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1

Uranium Enrichment Decontamination and Decommissioning Fund's...  

Broader source: Energy.gov (indexed) [DOE]

Uranium Enrichment Decontamination and Decommissioning Fund's Fiscal Year 2008 and 2007 Financial Statement Audit Uranium Enrichment Decontamination and Decommissioning Fund's...

2

Uranium enrichment decontamination and decommissioning fund, 1995 report  

SciTech Connect (OSTI)

This report describes strategies for the decontamination and decommissioning of gaseous diffusion plants. Progress in remedial action activities are discussed.

NONE

1996-11-01T23:59:59.000Z

3

Office of Environmental Management Uranium Enrichment Decontamination and Decommissioning Fund financial statements, September 30, 1995 and 1994  

SciTech Connect (OSTI)

The Energy Policy Act of 1992 (Act) requires the Department of Energy to retain ownership and responsibility for the costs of environmental cleanup resulting from the Government`s operation of the three gaseous diffusion facilities located at the K-25 site in Oak Ridge, Tennessee; Paducah, Kentucky; and Portsmouth, Ohio. The Act transferred the uranium enrichment enterprise to the United States Enrichment Corporation (USEC) as of July 1, 1993, and established the Uranium Enrichment Decontamination and Decommissioning Fund (D&D Fund) to: Pay for the costs of decontamination and decommissioning at the diffusion facilities; pay the annual costs for remedial action at the diffusion facilities to the extent that the amount in the Fund is sufficient; and reimburse uranium/thorium licensees for the costs of decontamination, decommissioning, reclamation, and other remedial actions which are incident to sales to the Government.

NONE

1996-02-21T23:59:59.000Z

4

Office of Environmental Management uranium enrichment decontamination and decommissioning fund financial statements. September 30, 1994 and 1993  

SciTech Connect (OSTI)

The Energy Policy Act of 1992 (Act) transferred the uranium enrichment enterprise to the United States Enrichment Corporation as of July 1, 1993. However, the Act requires the Department of Energy to retain ownership and responsibility for the costs of environmental cleanup resulting from the Government`s operation of the three gaseous diffusion facilities located in Oak Ridge, Tennessee; Paducah, Kentucky; and Portsmouth, Ohio (diffusion facilities). The Act established the Uranium Enrichment Decontamination and Decommissioning Fund (D&D Fund) to: Pay for the costs of decontamination and decommissioning at the diffusion facilities; Pay the annual costs for remedial action at the diffusion facilities to the extent that the amount in the Fund is sufficient; and Reimburse uranium/thorium licensees for the costs of decontamination, decommissioning, reclamation, and other remedial actions which are incident to sales to the Government.

Marwick, P.

1994-12-15T23:59:59.000Z

5

United States Department of Energy, Office of Environmental Management, Uranium Enrichment Decontamination and Decomissioning Fund financial statements, September 30, 1996 and 1995  

SciTech Connect (OSTI)

The Energy Policy Act of 1992 (Act) established the Uranium Enrichment Decontamination and Decommissioning Fund (D and D Fund, or Fund) to pay the costs for decontamination and decommissioning three gaseous diffusion facilities located in Oak Ridge, Tennessee; Paducah, Kentucky; and Portsmouth, Ohio (diffusion facilities). The Act also authorized the Fund to pay remedial action costs associated with the Government`s operation of the facilities and to reimburse uranium and thorium licensees for the costs of decontamination, decommissioning, reclamation, and other remedial actions which are incident to sales to the Government. The report presents the results of the independent certified public accountants` audit of the D and D Fund financial statements as of September 30, 1996. The auditors have expressed an unqualified opinion on the 1996 statement of financial position and the related statements of operations and changes in net position and cash flows.

NONE

1997-05-01T23:59:59.000Z

6

Uranium Enrichment Decontamination and Decommissioning Fund's Fiscal Year 2011 Financial Statement Audit  

Energy Savers [EERE]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Office of Inspector GeneralDepartment of EnergyofProject is on Track|Solar DecathlonManufacturing LoanMaterialUranium

7

IPNS enriched uranium booster target  

SciTech Connect (OSTI)

Since startup in 1981, IPNS has operated on a fully depleted /sup 238/U target. With the booster as in the present system, high energy protons accelerated to 450 MeV by the Rapid Cycling Synchrotron are directed at the target and by mechanisms of spallation and fission of the uranium, produce fast neutrons. The neutrons from the target pass into adjacent moderator where they slow down to energies useful for spectroscopy. The target cooling systems and monitoring systems have operated very reliably and safely during this period. To provide higher neutron intensity, we have developed plans for an enriched uranium (booster) target. HETC-VIM calculations indicate that the target will produce approx.90 kW of heat, with a nominal x5 gain (k/sub eff/ = 0.80). The neutron beam intensity gain will be a factor of approx.3. Thermal-hydraulic and heat transport calculations indicate that approx.1/2 in. thick /sup 235/U discs are subject to about the same temperatures as the present /sup 238/U 1 in. thick discs. The coolant will be light demineralized water (H/sub 2/O) and the coolant flow rate must be doubled. The broadening of the fast neutron pulse width should not seriously affect the neutron scattering experiments. Delayed neutrons will appear at a level about 3% of the total (currently approx.0.5%). This may affect backgrounds in some experiments, so that we are assessing measures to control and correct for this (e.g., beam tube choppers). Safety analyses and neutronic calculations are nearing completion. Construction of the /sup 235/U discs at the ORNL Y-12 facility is scheduled to begin late 1985. The completion of the booster target and operation are scheduled for late 1986. No enriched uranium target assembly operating at the projected power level now exists in the world. This effort thus represents an important technological experiment as well as being a ''flux enhancer''.

Schulke, A.W. Jr.

1985-01-01T23:59:59.000Z

8

Toxic Substances Control Act Uranium Enrichment Federal Facility...  

Office of Environmental Management (EM)

Toxic Substances Control Act Uranium Enrichment Federal Facility Compliance Agreement Toxic Substances Control Act Uranium Enrichment Federal Facility Compliance Agreement Toxic...

9

Highly Enriched Uranium Materials Facility, Major Design Changes...  

Energy Savers [EERE]

Highly Enriched Uranium Materials Facility, Major Design Changes Late...Lessons Learned Report, NNSA, Dec 2010 Highly Enriched Uranium Materials Facility, Major Design Changes...

10

EIS-0329: Proposed Construction, Operation, Decontamination/Decommissioning of Depleted Uranium Hexafluoride Conversion Facilities  

Broader source: Energy.gov [DOE]

This EIS analyzes DOE's proposal to construct, operate, maintain, and decontaminate and decommission two depleted uranium hexafluoride (DUF 6) conversion facilities, at Portsmouth, Ohio, and Paducah, Kentucky.

11

Uncertainty clouds uranium enrichment corporation's plans  

SciTech Connect (OSTI)

An expected windfall to the US Treasury from the sale of the Energy Dept.'s commercial fuel enrichment facilities may evaporate in the next few weeks when the Clinton administration submits its fiscal 1994 budget proposal to Congress, according to congressional and administration officials. Under the Energy Policy Act of 1992, DOE is required to lease two uranium enrichment facilities, Portsmouth, Ohio, and Paducah, KY., to the government-owned US Enrichment Corp. (USEC) by July 1. Estimates by OMB and Treasury indicate a potential yearly payoff of $300 million from the government-owned company's sale of fuel for commercial reactors. Those two facilities use a process of gaseous diffusion to enrich uranium to about 3 percent for use as fuel in commercial power plants. DOE has contracts through at least 1996 to provide about 12 million separative work units (SWUs) yearly to US utilities and others world-wide. But under an agreement signed between the US and Russia last August, at least 10 metric tons, or 1.5 million SWUs, of low-enriched uranium (LEU) blended down from Russia warheads is expected to be delivered to the US starting in 1994. It could be sold at $50 to $60 per SWU, far below what DOE currently charges for its SWUs - $135 per SWU for 70 percent of the contract price and $90 per SWU for the remaining 30 percent.

Lane, E.

1993-03-24T23:59:59.000Z

12

Conversion and Blending Facility Highly enriched uranium to low enriched uranium as uranium hexafluoride. Revision 1  

SciTech Connect (OSTI)

This report describes the Conversion and Blending Facility (CBF) which will have two missions: (1) convert surplus HEU materials to pure HEU UF{sub 6} and a (2) blend the pure HEU UF{sub 6} with diluent UF{sub 6} to produce LWR grade LEU-UF{sub 6}. The primary emphasis of this blending be to destroy the weapons capability of large, surplus stockpiles of HEU. The blended LEU product can only be made weapons capable again by the uranium enrichment process. The chemical and isotopic concentrations of the blended LEU product will be held within the specifications required for LWR fuel. The blended LEU product will be offered to the United States Enrichment Corporation (USEC) to be sold as feed material to the commercial nuclear industry.

NONE

1995-07-05T23:59:59.000Z

13

Evaporation of Enriched Uranium Solutions Containing Organophosphates  

SciTech Connect (OSTI)

The Savannah River Site has enriched uranium (EU) solution which has been stored for almost 10 years since being purified in the second uranium cycle of the H area solvent extraction process. The preliminary SRTC data, in conjunction with information in the literature, is promising. However, very few experiments have been run, and none of the results have been confirmed with repeat tests. As a result, it is believed that insufficient data exists at this time to warrant Separations making any process or program changes based on the information contained in this report. When this data is confirmed in future testing, recommendations will be presented.

Pierce, R.A.

1999-03-18T23:59:59.000Z

14

Uranium enrichment export control guide: Gaseous diffusion  

SciTech Connect (OSTI)

This document was prepared to serve as a guide for export control officials in their interpretation, understanding, and implementation of export laws that relate to the Zangger International Trigger List for gaseous diffusion uranium enrichment process components, equipment, and materials. Particular emphasis is focused on items that are especially designed or prepared since export controls are required for these by States that are party to the International Nuclear Nonproliferation Treaty.

Not Available

1989-09-01T23:59:59.000Z

15

Conversion and Blending Facility highly enriched uranium to low enriched uranium as metal. Revision 1  

SciTech Connect (OSTI)

The mission of this Conversion and Blending Facility (CBF) will be to blend surplus HEU metal and alloy with depleted uranium metal to produce an LEU product. The primary emphasis of this blending operation will be to destroy the weapons capability of large, surplus stockpiles of HEU. The blended LEU product can only be made weapons capable again by the uranium enrichment process. The blended LEU will be produced as a waste suitable for storage or disposal.

NONE

1995-07-05T23:59:59.000Z

16

NNSA Authorizes Start-Up of Highly Enriched Uranium Materials...  

National Nuclear Security Administration (NNSA)

Authorizes Start-Up of Highly Enriched Uranium Materials Facility at Y-12 | National Nuclear Security Administration Facebook Twitter Youtube Flickr RSS People Mission Managing the...

17

An Optically Stimulated Luminescence Uranium Enrichment Monitor  

SciTech Connect (OSTI)

The Pacific Northwest National Laboratory (PNNL) has pioneered the use of Optically Stimulated Luminescence (OSL) technology for use in personnel dosimetry and high dose radiation processing dosimetry. PNNL has developed and patented an alumina-based OSL dosimeter that is being used by the majority of medical X-ray and imaging technicians worldwide. PNNL has conceived of using OSL technology to passively measure the level of UF6 enrichment by attaching the prototype OSL monitor to pipes containing UF6 gas within an enrichment facility. The prototype OSL UF6 monitor utilizes a two-element approach with the first element open and unfiltered to measure both the low energy and high energy gammas from the UF6, while the second element utilizes a 3-mm thick tungsten filter to eliminate the low energy gammas and pass only the high energy gammas from the UF6. By placing a control monitor in the room away from the UF6 pipes and other ionizing radiation sources, the control readings can be subtracted from the UF6 pipe monitor measurements. The ratio of the shielded to the unshielded net measurements provides a means to estimate the level of uranium enrichment. PNNL has replaced the commercially available MicroStar alumina-based dosimeter elements with a composite of polyethylene plastic, high-Z glass powder, and BaFBr:Eu OSL phosphor powder at various concentrations. The high-Z glass was added in an attempt to raise the average “Z” of the composite dosimeter and increase the response. Additionally, since BaFBr:Eu OSL phosphor is optimally excited and emits light at different wavelengths compared to alumina, the commercially available MicroStar reader was modified for reading BaFBr:Eu in a parallel effort to increase reader sensitivity. PNNL will present the design and performance of our novel OSL uranium enrichment monitor based on a combination of laboratory and UF6 test loop measurements. PNNL will also report on the optimization effort to achieve the highest possible performance from both the OSL enrichment monitor and the new custom OSL reader modified for this application. This project has been supported by the US Department of Energy’s National Nuclear Security Administration’s Office of Dismantlement and Transparency (DOE/NNSA/NA-241).

Miller, Steven D.; Tanner, Jennifer E.; Simmons, Kevin L.; Conrady, Matthew M.; Benz, Jacob M.; Greenfield, Bryce A.

2010-08-11T23:59:59.000Z

18

Measurement of uranium enrichment by gamma spectroscopy: result of an experimental design  

E-Print Network [OSTI]

, Gamma Spectrometry, uranium enrichment #12;PAPER Measurement of uranium enrichment by gamma spectroscopy: result of an experimental design Gamma spectroscopy is commonly used in nuclear safeguards to measure uranium enrichment. An experimental

19

The uranium cylinder assay system for enrichment plant safeguards  

SciTech Connect (OSTI)

Safeguarding sensitive fuel cycle technology such as uranium enrichment is a critical component in preventing the spread of nuclear weapons. A useful tool for the nuclear materials accountancy of such a plant would be an instrument that measured the uranium content of UF{sub 6} cylinders. The Uranium Cylinder Assay System (UCAS) was designed for Japan Nuclear Fuel Limited (JNFL) for use in the Rokkasho Enrichment Plant in Japan for this purpose. It uses total neutron counting to determine uranium mass in UF{sub 6} cylinders given a known enrichment. This paper describes the design of UCAS, which includes features to allow for unattended operation. It can be used on 30B and 48Y cylinders to measure depleted, natural, and enriched uranium. It can also be used to assess the amount of uranium in decommissioned equipment and waste containers. Experimental measurements have been carried out in the laboratory and these are in good agreement with the Monte Carlo modeling results.

Miller, Karen A [Los Alamos National Laboratory; Swinhoe, Martyn T [Los Alamos National Laboratory; Marlow, Johnna B [Los Alamos National Laboratory; Menlove, Howard O [Los Alamos National Laboratory; Rael, Carlos D [Los Alamos National Laboratory; Iwamoto, Tomonori [JNFL; Tamura, Takayuki [JNFL; Aiuchi, Syun [JNFL

2010-01-01T23:59:59.000Z

20

Conversion and Blending Facility highly enriched uranium to low enriched uranium as oxide. Revision 1  

SciTech Connect (OSTI)

This Conversion and Blending Facility (CBF) will have two missions: (1) convert HEU materials into pure HEU oxide and (2) blend the pure HEU oxide with depleted and natural uranium oxide to produce an LWR grade LEU product. The primary emphasis of this blending operation will be to destroy the weapons capability of large, surplus stockpiles of HEU. The blended LEU product can only be made weapons capable again by the uranium enrichment process. To the extent practical, the chemical and isotopic concentrations of blended LEU product will be held within the specifications required for LWR fuel. Such blended LEU product will be offered to the United States Enrichment Corporation (USEC) to be sold as feed material to the commercial nuclear industry. Otherwise, blended LEU will be produced as a waste suitable for storage or disposal.

NONE

1995-07-05T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


21

Basic characterization of highly enriched uranium by gamma spectrometry  

E-Print Network [OSTI]

Gamma-spectrometric methods suitable for the characterization of highly enriched uranium samples encountered in illicit trafficking of nuclear materials are presented. In particular, procedures for determining the 234U, 235U, 238U, 232U and 236U contents and the age of highly enriched uranium are described. Consequently, the total uranium content and isotopic composition can be calculated. For determining the 238U and 232U contents a low background chamber was used. In addition, age dating of uranium was also performed using low-background spectrometry.

Cong Tam Nguyen; Jozsef Zsigrai

2005-08-25T23:59:59.000Z

22

Basic characterization of highly enriched uranium by gamma spectrometry  

E-Print Network [OSTI]

Gamma-spectrometric methods suitable for the characterization of highly enriched uranium samples encountered in illicit trafficking of nuclear materials are presented. In particular, procedures for determining the 234U, 235U, 238U, 232U and 236U contents and the age of highly enriched uranium are described. Consequently, the total uranium content and isotopic composition can be calculated. For determining the 238U and 232U contents a low background chamber was used. In addition, age dating of uranium was also performed using low-background spectrometry.

Nguyen, C T

2006-01-01T23:59:59.000Z

23

Production of Mo-99 using low-enriched uranium silicide  

SciTech Connect (OSTI)

Over the last several years, uranium silicide fuels have been under development as low-enriched uranium (LEU) targets for Mo-99. The use of LEU silicide is aimed at replacing the UAl{sub x} alloy in the highly-enriched uranium dissolution process. A process to recover Mo-99 from low-enriched uranium silicide is being developed at Argonne National Laboratory. The uranium silicide is dissolved in alkaline hydrogen peroxide. Experiments performed to determine the optimum dissolution procedure are discussed, and the results of dissolving a portion of a high-burnup (>40%) U{sub 3}Si{sub 2} miniplate are presented. Future work related to Mo-99 separation and waste disposal are also discussed.

Hutter, J. C.; Srinivasan, B.; Vicek, M.; Vandegrift, G. F.

1994-09-01T23:59:59.000Z

24

Surface Decontamination of System Components in Uranium Conversion Plant at KAERI  

SciTech Connect (OSTI)

A chemical decontamination process using nitric acid solution was selected as in-situ technology for recycle or release with authorization of a large amount of metallic waste including process system components such as tanks, piping, etc., which is generated by dismantling a retired uranium conversion plant at Korea Atomic Energy Research Institute (KAERI). The applicability of nitric acid solution for surface decontamination of metallic wastes contaminated with uranium compounds was evaluated through the basic research on the dissolution of UO2 and ammonium uranyl carbonate (AUC) powder. Decontamination performance was verified by using the specimens contaminated with such uranium compounds as UO2 and AUC taken from the uranium conversion plant. Dissolution rate of UO2 powder is notably enhanced by the addition of H2O2 as an oxidant even in the condition of a low concentration of nitric acid and low temperature compared with those in a nitric acid solution without H2O2. AUC powders dissolve easily in nitric acid solutions until the solution pH attains about 2.5 {approx} 3. Above that solution pH, however, the uranium concentration in the solution is lowered drastically by precipitation as a form of U3(NH3)4O9 . 5H2O. Decontamination performance tests for the specimens contaminated with UO2 and AUC were quite successful with the application of decontamination conditions obtained through the basic studies on the dissolution of UO2 and AUC powders.

Choi, W. K.; Kim, K. N.; Won, H. J.; Jung, C. H.; Oh, W. Z.

2003-02-25T23:59:59.000Z

25

Examination of the conversion of the U.S. submarine fleet from highly enriched uranium to low enriched uranium  

E-Print Network [OSTI]

The nuclear reactors used by the U.S. Navy for submarine propulsion are currently fueled by highly enriched uranium (HEU), but HEU brings administrative and political challenges. This issue has been studied by the Navy ...

McCord, Cameron (Cameron Liam)

2014-01-01T23:59:59.000Z

26

The IMCA: A field instrument for uranium enrichment measurements  

SciTech Connect (OSTI)

The IMCA (Inspection Multi-Channel Analyzer) is a portable gamma-ray spectrometer designed to measure the enrichment of uranium either in a laboratory or in the field. The IMCA consists of a Canberra InSpector Multi-Channel Analyzer, sodium iodide or a planar germanium detector, and special application software. The system possesses a high degree of automation. The IMCA uses the uranium enrichment meter principle, and is designed to meet the International Atomic Energy Agency (IAEA) requirements for the verification of enriched uranium materials. The IMCA is available with MGA plutonium isotopic analysis software or MGAU uranium analysis software as well. In this paper, the authors present a detailed description of the hardware and software of the IMCA system, as well as results from preliminary measurements testing compliance of IMCA with IAEA requirements using uranium standards and UF6 cylinders. Measurements performed on UF6 cylinders in the field under variable environmental conditions (temperatures ranging from 0 to 35 C) have shown that good results can be achieved. The enrichment of UF6 contained in the cylinder is determined by using calibration constants generated from an instrument calibration, using traceable uranium oxide standards, performed in the laboratory under controlled environmental conditions. The IMCA software is designed to make the necessary matrix and container corrections to ensure that accurate results are achieved in the field.

Gardner, G.H.; Koskelo, M.; Moeslinger, M. [Canberra Industries, Meriden, CT (United States); Mayer, R.L. II; McGinnis, B.R. [Lockheed Martin Utility Services, Piketon, OH (United States). Portsmouth Gaseous Diffusion Plant; Wishard, B. [International Atomic Energy Agency, Vienna (Austria)

1996-12-31T23:59:59.000Z

27

EA-1172: Sale of Surplus Natural and Low Enriched Uranium, Piketon, Ohio  

Broader source: Energy.gov [DOE]

This EA evaluates the environmental impacts for the proposal to sell uranium for subsequent enrichment and fabrication into commercial nuclear power reactor fuel.  The uranium is currently stored...

28

Chapter 20 - Uranium Enrichment Decontamination & Decommissioning Fund  

Energy Savers [EERE]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious RankCombustion |Energyon ArmedWaste andAccessCO2 Injection Begins8: Variable Frequency Drive2: Commercial

29

Uranium Enrichment Decontamination and Decommissioning Fund's Fiscal Year  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious RankCombustion |Energy Usage »of EnergyTheTwo New12.'6/0.2 ...... 13:27DepartmentUpdatingMaterial2008

30

Development of a low enrichment uranium core for the MIT reactor  

E-Print Network [OSTI]

An investigation has been made into converting the MIT research reactor from using high enrichment uranium (HEU) to low enrichment uranium (LEU) with a newly developed fuel material. The LEU fuel introduces negative ...

Newton, Thomas Henderson

2006-01-01T23:59:59.000Z

31

CRAD, Training- Y-12 Enriched Uranium Operations Oxide Conversion Facility  

Broader source: Energy.gov [DOE]

A section of Appendix C to DOE G 226.1-2 "Federal Line Management Oversight of Department of Energy Nuclear Facilities." Consists of Criteria Review and Approach Documents (CRADs) used for a January 2005 assessment of the Training Program at the Y-12 - Enriched Uranium Operations Oxide Conversion Facility.

32

CRAD, Management- Y-12 Enriched Uranium Operations Oxide Conversion Facility  

Broader source: Energy.gov [DOE]

A section of Appendix C to DOE G 226.1-2 "Federal Line Management Oversight of Department of Energy Nuclear Facilities." Consists of Criteria Review and Approach Documents (CRADs) used for a January 2005 assessment of Management program at the Y-12 - Enriched Uranium Operations Oxide Conversion Facility.

33

Thermal hydraulics analysis of the MIT research reactor in support of a low enrichment uranium (LEU) core conversion .  

E-Print Network [OSTI]

??The MIT research reactor (MITR) is converting from the existing high enrichment uranium (HEU) core to a low enrichment uranium (LEU) core using a high-density… (more)

Ko, Yu-Chih, Ph. D. Massachusetts Institute of Technology

2008-01-01T23:59:59.000Z

34

SciTech Connect: enriched uranium  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administrationcontroller systemsBi (2) Sr (2) CawithMicrofluidicJournalWhat is aenriched uranium

35

Criticality Safety of Low-Enriched Uranium and High-Enriched Uranium Fuel Elements in Heavy Water Lattices  

SciTech Connect (OSTI)

The RB reactor was designed as a natural-uranium, heavy water, nonreflected critical assembly in the Vinca Institute of Nuclear Sciences, Belgrade, Yugoslavia, in 1958. From 1962 until 2002, numerous critical experiments were carried out with low-enriched uranium and high-enriched uranium fuel elements of tubular shape, known as the Russian TVR-S fuel assembly type, placed in various heavy water square lattices within the RB cylindrical aluminum tank. Some of these well-documented experiments were selected, described, evaluated, and accepted for inclusion in the 'International Handbook of Evaluated Criticality Safety Benchmark Experiments', contributing to the preservation of a rather small number of heavy water benchmark critical experiments.

Pesic, Milan P

2003-10-15T23:59:59.000Z

36

Simulation of transportation of low enriched uranium solutions  

SciTech Connect (OSTI)

A simulation of the transportation by truck of low enriched uranium solutions has been completed for NEPA purposes at the Savannah River Site. The analysis involves three distinct source terms, and establishes the radiological risks of shipment to three possible destinations. Additionally, loading accidents were analyzed to determine the radiological consequences of mishaps during handling and delivery. Source terms were developed from laboratory measurements of chemical samples from low enriched uranium feed materials being stored at SRS facilities, and from manufacturer data on transport containers. The transportation simulations were accomplished over the INTERNET using the DOE TRANSNET system at Sandia National Laboratory. The HIGHWAY 3.3 code was used to analyze routing scenarios, and the RADTRAN 4 code was used to analyze incident free and accident risks of transporting radiological materials. Loading accidents were assessed using the Savannah River Site AXAIR89Q and RELEASE 2 codes.

Hope, E.P.; Ades, M.J.

1996-08-01T23:59:59.000Z

37

High Accuracy U-235 Enrichment Verification Station for Low Enriched Uranium Alloys  

SciTech Connect (OSTI)

The Y-12 National Security Complex is playing a role in the U.S. High Performance Research Reactor (USHPRR) Conversion program sponsored by the U.S. National Nuclear Security Administration's Office of Global Threat Reduction. The USHPRR program has a goal of converting remaining U.S. reactors that continue to use highly enriched uranium (HEU) fuel to low enriched uranium (LEU) fuel. The USHPRR program is currently developing a LEU Uranium-Molybdenum (U-Mo) monolithic fuel for use in the U.S. high performance research reactors.Y-12 is supporting both the fuel development and fuel fabrication efforts by fabricating low enriched U-Mo foils from its own source material for irradiation experiments and for optimizing the fabrication process in support of scaling up the process to a commercial production scale. Once the new fuel is qualified, Y-12 will produce and ship U-Mo coupons with verified 19.75% +0.2% - 0.3% U-235 enrichment to be fabricated into fuel elements for the USHPRRs. Considering this small enrichment tolerance and the transition into HEU being set strictly at 20% U-235, a characterization system with a measurement uncertainty of less than or equal to 0.1% in enrichment is desired to support customer requirements and minimize production costs. Typical uncertainty for most available characterization systems today is approximately 1-5%; therefore, a specialized system must be developed which results in a reduced measurement uncertainty. A potential system using a High-Purity Germanium (HPGe) detector has been procured, and tests have been conducted to verify its capabilities with regards to the requirements. Using four U-Mo enrichment standards fabricated with complete isotopic and chemical characterization, infinite thickness and peak-ratio enrichment measurement methods have been considered for use. As a result of inhomogeneity within the U-Mo samples, FRAM, an isotopic analysis software, has been selected for initial testing. A systematic approach towards observing effects on FRAM's enrichment analysis has been conducted with regards to count and dead time.

Lillard, C. R.; Hayward, J. P.; Williamson, M. R.

2012-06-07T23:59:59.000Z

38

Natural uranium/conversion services/enrichment services  

SciTech Connect (OSTI)

This article is the 1993 uranium market summary. During this reporting period, there were 50 deals in the concentrates market, 26 deals in the UF6 market, and 14 deals for enrichment services. In the concentrates market, the restricted value closed $0.15 higher at $9.85, and the unrestricted value closed down $0.65 at $7.00. In the UF6 market, restricted prices fluctuated and closed higher at $31.00, and unrestricted prices closed at their initial value of $24.75. The restricted transaction value closed at $10.25 and the unrestricted value closed at $7.15. In the enrichment services market, the restricted value moved steadily higher to close at $84.00 per SWU, and the unrestricted value closed at its initial value of $68.00 per SWU.

NONE

1993-12-31T23:59:59.000Z

39

Accelerating the Reduction of Excess Russian Highly Enriched Uranium  

SciTech Connect (OSTI)

This paper presents the latest information on one of the Accelerated Highly Enriched Uranium (HEU) Disposition initiatives that resulted from the May 2002 Summit meeting between Presidents George W. Bush and Vladimir V. Putin. These initiatives are meant to strengthen nuclear nonproliferation objectives by accelerating the disposition of nuclear weapons-useable materials. The HEU Transparency Implementation Program (TIP), within the National Nuclear Security Administration (NNSA) is working to implement one of the selected initiatives that would purchase excess Russian HEU (93% 235U) for use as fuel in U.S. research reactors over the next ten years. This will parallel efforts to convert the reactors' fuel core from HEU to low enriched uranium (LEU) material, where feasible. The paper will examine important aspects associated with the U.S. research reactor HEU purchase. In particular: (1) the establishment of specifications for the Russian HEU, and (2) transportation safeguard considerations for moving the HEU from the Mayak Production Facility in Ozersk, Russia, to the Y-12 National Security Complex in Oak Ridge, TN.

Benton, J; Wall, D; Parker, E; Rutkowski, E

2004-02-18T23:59:59.000Z

40

International Atomic Energy Agency support of research reactor highly enriched uranium to low enriched uranium fuel conversion projects  

SciTech Connect (OSTI)

The IAEA has been involved for more than twenty years in supporting international nuclear non- proliferation efforts associated with reducing the amount of highly enriched uranium (HEU) in international commerce. IAEA projects and activities have directly supported the Reduced Enrichment for Research and Test Reactors (RERTR) programme, as well as directly assisted efforts to convert research reactors from HEU to LEU fuel. HEU to LEU fuel conversion projects differ significantly depending on several factors including the design of the reactor and fuel, technical needs of the member state, local nuclear infrastructure, and available resources. To support such diverse endeavours, the IAEA tailors each project to address the relevant constraints. This paper presents the different approaches taken by the IAEA to address the diverse challenges involved in research reactor HEU to LEU fuel conversion projects. Examples of conversion related projects in different Member States are fully detailed. (author)

Bradley, E.; Adelfang, P.; Goldman, I.N. [Research Reactors Unit, Division of Nuclear Fuel Cycle and Waste Technology, International Atomic Energy Agency, Wagramer Strasse 5, P.O. Box 100, A-1400 Vienna (Austria)

2008-07-15T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


41

Conversion and Blending Facility highly enriched uranium to low enriched uranium as uranyl nitrate hexahydrate. Revision 1  

SciTech Connect (OSTI)

This Conversion and Blending Facility (CBF) will have two missions: (1) convert HEU materials to pure HEU uranyl nitrate (UNH) and (2) blend pure HEU UNH with depleted and natural UNH to produce HEU UNH crystals. The primary emphasis of this blending operation will be to destroy the weapons capability of large, surplus stockpiles of HEU. The blended LEU product can only be made weapons capable again by the uranium enrichment process. To the extent practical, the chemical and isotopic concentrations of blended LEU product will be held within the specifications required for LWR fuel. Such blended LEU product will be offered to the United States Enrichment Corporation (USEC) to be sold as feed material to the commercial nuclear industry. Otherwise, blended LEU Will be produced as a waste suitable for storage or disposal.

NONE

1995-07-05T23:59:59.000Z

42

Uranium mineralization in fluorine-enriched volcanic rocks  

SciTech Connect (OSTI)

Several uranium and other lithophile element deposits are located within or adjacent to small middle to late Cenozoic, fluorine-rich rhyolitic dome complexes. Examples studied include Spor Mountain, Utah (Be-U-F), the Honeycomb Hills, Utah (Be-U), the Wah Wah Mountains, Utah (U-F), and the Black Range-Sierra Cuchillo, New Mexico (Sn-Be-W-F). The formation of these and similar deposits begins with the emplacement of a rhyolitic magma, enriched in lithophile metals and complexing fluorine, that rises to a shallow crustal level, where its roof zone may become further enriched in volatiles and the ore elements. During initial explosive volcanic activity, aprons of lithicrich tuffs are erupted around the vents. These early pyroclastic deposits commonly host the mineralization, due to their initial enrichment in the lithophile elements, their permeability, and the reactivity of their foreign lithic inclusions (particularly carbonate rocks). The pyroclastics are capped and preserved by thick topaz rhyolite domes and flows that can serve as a source of heat and of additional quantities of ore elements. Devitrification, vapor-phase crystallization, or fumarolic alteration may free the ore elements from the glassy matrix and place them in a form readily leached by percolating meteoric waters. Heat from the rhyolitic sheets drives such waters through the system, generally into and up the vents and out through the early tuffs. Secondary alteration zones (K-feldspar, sericite, silica, clays, fluorite, carbonate, and zeolites) and economic mineral concentrations may form in response to this low temperature (less than 200 C) circulation. After cooling, meteoric water continues to migrate through the system, modifying the distribution and concentration of the ore elements (especially uranium).

Burt, D.M.; Sheridan, M.F.; Bikun, J.; Christiansen, E.; Correa, B.; Murphy, B.; Self, S.

1980-09-01T23:59:59.000Z

43

New Prototype Safeguards Technology Offers Improved Confidence and Automation for Uranium Enrichment Facilities  

SciTech Connect (OSTI)

An important requirement for the international safeguards community is the ability to determine the enrichment level of uranium in gas centrifuge enrichment plants and nuclear fuel fabrication facilities. This is essential to ensure that countries with nuclear nonproliferation commitments, such as States Party to the Nuclear Nonproliferation Treaty, are adhering to their obligations. However, current technologies to verify the uranium enrichment level in gas centrifuge enrichment plants or nuclear fuel fabrication facilities are technically challenging and resource-intensive. NNSA’s Office of Nonproliferation and International Security (NIS) supports the development, testing, and evaluation of future systems that will strengthen and sustain U.S. safeguards and security capabilities—in this case, by automating the monitoring of uranium enrichment in the entire inventory of a fuel fabrication facility. One such system is HEVA—hybrid enrichment verification array. This prototype was developed to provide an automated, nondestructive assay verification technology for uranium hexafluoride (UF6) cylinders at enrichment plants.

Brim, Cornelia P.

2013-04-01T23:59:59.000Z

44

New Prototype Safeguards Technology Offers Improved Confidence and Automation for Uranium Enrichment Facilities  

SciTech Connect (OSTI)

An important requirement for the international safeguards community is the ability to determine the enrichment level of uranium in gas centrifuge enrichment plants and nuclear fuel fabrication facilities. This is essential to ensure that countries with nuclear nonproliferation commitments, such as States Party to the Nuclear Nonproliferation Treaty, are adhering to their obligations. However, current technologies to verify the uranium enrichment level in gas centrifuge enrichment plants or nuclear fuel fabrication facilities are technically challenging and resource-intensive. NNSA’s Office of Nonproliferation and International Security (NIS) supports the development, testing, and evaluation of future systems that will strengthen and sustain U.S. safeguards and security capabilities—in this case, by automating the monitoring of uranium enrichment in the entire inventory of a fuel fabrication facility. One such system is HEVA—hybrid enrichment verification array. This prototype was developed to provide an automated, nondestructive assay verification technology for uranium hexafluoride (UF6) cylinders at enrichment plants.

Brim, Cornelia P.

2013-03-04T23:59:59.000Z

45

Progress in alkaline peroxide dissolution of low-enriched uranium metal and silicide targets  

SciTech Connect (OSTI)

This paper reports recent progress on two alkaline peroxide dissolution processes: the dissolution of low-enriched uranium metal and silicide (U{sub 3}Si{sub 2}) targets. These processes are being developed to substitute low-enriched for high-enriched uranium in targets used for production of fission-product {sup 99}Mo. Issues that are addressed include (1) dissolution kinetics of silicide targets, (2) {sup 99}Mo lost during aluminum dissolution, (3) modeling of hydrogen peroxide consumption, (4) optimization of the uranium foil dissolution process, and (5) selection of uranium foil barrier materials. Future work associated with these two processes is also briefly discussed.

Chen, L.; Dong, D.; Buchholz, B.A.; Vandegrift, G.F. [Argonne National Lab., IL (United States). Chemical Technology Div.; Wu, D. [Univ. of Illinois, Urbana, IL (United States)

1996-12-31T23:59:59.000Z

46

Thermal hydraulic limits analysis for the MIT Research Reactor low enrichment uranium core conversion using statistical propagation of parametric uncertainties  

E-Print Network [OSTI]

The MIT Research Reactor (MITR) is evaluating the conversion from highly enriched uranium (HEU) to low enrichment uranium (LEU) fuel. In addition to the fuel element re-design from 15 to 18 plates per element, a reactor ...

Chiang, Keng-Yen

2012-01-01T23:59:59.000Z

47

Estimate of radiation release from MIT reactor with low enriched uranium (LEU) core during maximum hypothetical accident  

E-Print Network [OSTI]

In accordance with a 1986 NRC ruling, the MIT Research Reactor (MITR) is planning on converting from the use of highly enriched uranium (HEU) to low enriched uranium (LEU) for fuel. A component of the conversion analysis ...

Plumer, Kevin E. (Kevin Edward)

2011-01-01T23:59:59.000Z

48

Validation of NCSSHP for highly enriched uranium systems containing beryllium  

SciTech Connect (OSTI)

This document describes the validation of KENO V.a using the 27-group ENDF/B-IV cross section library for highly enriched uranium and beryllium neutronic systems, and is in accordance with ANSI/ANS-8.1-1983(R1988) requirements for calculational methods. The validation has been performed on a Hewlett Packard 9000/Series 700 Workstation at the Oak Ridge Y-12 Plant Nuclear Criticality Safety Department using the Oak Ridge Y-12 Plant Nuclear Criticality Safety Software code package. Critical experiments from LA-2203, UCRL-4975, ORNL-2201, and ORNL/ENG-2 have been identified as having the constituents desired for this validation as well as sufficient experimental detail to allow accurate construction of KENO V.a calculational models. The results of these calculations establish the safety criteria to be employed in future calculational studies of these types of systems.

Krass, A.W.; Elliott, E.P.; Tollefson, D.A.

1994-09-29T23:59:59.000Z

49

Methods for nondestructive assay holdup measurements in shutdown uranium enrichment facilities  

SciTech Connect (OSTI)

Measurement surveys of uranium holdup using nondestructive assay (NDA) techniques are being conducted for shutdown gaseous diffusion facilities at the Oak Ridge K-25 Site (formerly the Oak Ridge Gaseous Diffusion Plant). When in operation, these facilities processed UF{sub 6} with enrichments ranging from 0.2 to 93 wt % {sup 235}U. Following final shutdown of all process facilities, NDA surveys were initiated to provide process holdup data for the planning and implementation of decontamination and decommissioning activities. A three-step process is used to locate and quantify deposits: (1) high-resolution gamma-ray measurements are performed to generally define the relative abundances of radioisotopes present, (2) sizable deposits are identified using gamma-ray scanning methods, and (3) the deposits are quantified using neutron measurement methods. Following initial quantitative measurements, deposit sizes are calculated; high-resolution gamma-ray measurements are then performed on the items containing large deposits. The quantitative estimates for the large deposits are refined on the basis of these measurements. Facility management is using the results of the survey to support a variety of activities including isolation and removal of large deposits; performing health, safety, and environmental analyses; and improving facility nuclear material control and accountability records. 3 refs., 1 tab.

Hagenauer, R.C.; Mayer, R.L. II.

1991-09-01T23:59:59.000Z

50

EVALUATION OF FLOWSHEET CHANGES FOR THE HIGHLY ENRICHED URANIUM BLENDDOWN PROGRAM  

SciTech Connect (OSTI)

H Canyon is considering a flowsheet change for Plutonium (Pu) Contaminated Scrap (PuCS) material. The proposed change is to route dissolved PuCS material directly to a uranium (U) storage tank. As a result, the PuCS solution will bypass Head End and First U Cycle, and will be purified by solvent extraction in Second U Cycle. The PuCS solution contains appreciable amounts of boron (B) and fluoride (F{sup -}), which are currently at trace levels in the U storage tank. Though unlikely, if the B concentration in the U storage tank were to reach 1.8 g B/g U, the entire contents of the U storage tank would likely require a second pass through Second U Cycle to provide sufficient decontamination to meet the Tennessee Valley Authority (TVA) Blend Grade Highly Enriched Uranium (HEU) specification for B, which is 30 {micro}g/g U. In addition, Second U Cycle is expected to provide sufficient decontamination of F{sup -} and Pu regardless of the amount of PuCS solution sent to the storage tank. Though aluminum (Al) is not present in the PuCS solution, B can be credited as a complexant of F{sup -}. Both stability constants from the literature and Savannah River National Laboratory (SRNL) corrosion studies were documented to demonstrate that B complexation of F{sup -} in nitric acid solutions is sufficient to prevent excessive corrosion. Though B and Al complex F{sup -} to a similar degree, neither completely eliminates the presence of free F{sup -} in solution. Therefore, a limited amount of corrosion is expected even with complexed F{sup -} solutions. Tanks maintained at ambient temperature are not expected to experience significant corrosion. However, the Low Activity Waste (LAW) evaporators may be subjected to a corrosion rate of about 25 mils per year (mpy) as they reach their highest F{sup -} concentrations. The feed adjustment evaporator would only be subjected to the corrosion rate of about 25 mpy in the latter stages of the PuCS campaign. An issue that must be addressed as part of the proposed PuCS flowsheet change is that B has limited solubility in concentrated nitric acid solutions. As the proposed PuCS campaign progresses, the B concentration will increase in the U storage tank, in Second U Cycle feed, and in the 1DW stream sent to the LAW evaporators. Limitations on the B concentration in the LAW evaporators will be needed to prevent formation of boron-containing solids.

Crowder, M.; Rudisill, T.; Laurinat, J.; Mickalonis, J.

2007-10-22T23:59:59.000Z

51

S. 2415: Title I may be cited as the Uranium Enrichment Act of 1990; Title II may be cited as the Uranium Security and Tailings Reclamation Act of 1989; and Title III may be cited as The Solar, Wind, Waste, and Geothermal Power Production Incentives Act of 1990, introduced in the Senate, One Hundred First Congress, Second Session, April 4, 1990  

SciTech Connect (OSTI)

S. 2415 (which started out as a bill to encourage solar and geothermal power generation) now would amend the Atomic Energy Act of 1954 to redirect uranium enrichment enterprises to further the national interest, respond to competitive market forces, and to ensure the nation's common defense and security. It would establish a United States Enrichment Corporation for the following purposes: to acquire feed materials, enriched uranium, and enrichment facilities; to operate these facilities; to market enriched uranium for governmental purposes and qualified domestic and foreign persons; to conduct research into uranium enrichment; and to operate as a profitable, self-financing, reliable corporation and in a manner consistent with the health and safety of the public. The bill describes powers and duties of the corporation; the organization, finance, and management; decontamination and decommissioning. The second part of the bill would ensure an adequate supply of domestic uranium for defense and power production; provide assistance to the domestic uranium industry; and establish, facilitate, and expedite a comprehensive system for financing reclamation and remedial action at active uranium and thorium processing sites. The third part of the bill would remove the size limitations on power production facilities now part of the Public Utility Regulatory Policies Act of 1978. Solar, wind, waste, or geothermal power facilities would no longer have to be less than 80 MW to qualify as a small power production facility.

Not Available

1990-01-01T23:59:59.000Z

52

Standard specification for uranium hexafluoride enriched to less than 5 % 235U  

E-Print Network [OSTI]

1.1 This specification covers nuclear grade uranium hexafluoride (UF6) that either has been processed through an enrichment plant, or has been produced by the blending of Highly Enriched Uranium with other uranium to obtain uranium of any 235U concentration below 5 % and that is intended for fuel fabrication. The objectives of this specification are twofold: (1) To define the impurity and uranium isotope limits for Enriched Commercial Grade UF6 so that, with respect to fuel design and manufacture, it is essentially equivalent to enriched uranium made from natural UF6; and (2) To define limits for Enriched Reprocessed UF6 to be expected if Reprocessed UF6 is to be enriched without dilution with Commercial Natural UF6. For such UF6, special provisions, not defined herein, may be needed to ensure fuel performance and to protect the work force, process equipment, and the environment. 1.2 This specification is intended to provide the nuclear industry with a standard for enriched UF6 that is to be used in the pro...

American Society for Testing and Materials. Philadelphia

2010-01-01T23:59:59.000Z

53

Realities of verifying the absence of highly enriched uranium (HEU) in gas centrifuge enrichment plants  

SciTech Connect (OSTI)

Over a two and one-half year period beginning in 1981, representatives of six countries (United States, United Kingdom, Federal Republic of Germany, Australia, The Netherlands, and Japan) and the inspectorate organizations of the International Atomic Energy Agency and EURATOM developed and agreed to a technically sound approach for verifying the absence of highly enriched uranium (HEU) in gas centrifuge enrichment plants. This effort, known as the Hexapartite Safeguards Project (HSP), led to the first international concensus on techniques and requirements for effective verification of the absence of weapons-grade nuclear materials production. Since that agreement, research and development has continued on the radiation detection technology-based technique that technically confirms the HSP goal is achievable. However, the realities of achieving the HSP goal of effective technical verification have not yet been fully attained. Issues such as design and operating conditions unique to each gas centrifuge plant, concern about the potential for sensitive technology disclosures, and on-site support requirements have hindered full implementation and operator support of the HSP agreement. In future arms control treaties that may limit or monitor fissile material production, the negotiators must recognize and account for the realities and practicalities in verifying the absence of HEU production. This paper will describe the experiences and realities of trying to achieve the goal of developing and implementing an effective approach for verifying the absence of HEU production. 3 figs.

Swindle, D.W.

1990-03-01T23:59:59.000Z

54

Environmental Survey preliminary report, Portsmouth Uranium Enrichment Complex, Piketon, Ohio  

SciTech Connect (OSTI)

This report presents the preliminary findings from the first phase of the Environmental Survey of the United States Department of Energy (DOE) Portsmouth Uranium Enrichment Complex (PUEC), conducted August 4 through August 15, 1986. The Survey is being conducted by an interdisciplinary team of environmental specialists, led and managed by the Office of Environment, Safety and Health's Office of Environmental Audit. Team specialists are being supplied by a private contractor. The objective of the Survey is to identify environmental problems and areas of environmental regulation. It is being performed in accordance with the DOE Environmental Survey Manual. This phase of the Survey involves the review of existing site environmental data, observations of the operations performed at PUEC, and interviews with site personnel. The Survey team developed a Sampling and Analysis Plan to assist in further assessing certain of the environmental problems identified during its on-site activities. The Sampling and Analysis Plan will be executed by Argonne National Laboratory. When completed, the results will be incorporated into the PUEC Environmental Survey Interim Report. The Interim Report will reflect the final determinations of the PUEC Survey. 55 refs., 22 figs., 21 tabs.

Not Available

1987-08-01T23:59:59.000Z

55

Low-enriched uranium holdup measurements in Kazakhstan  

SciTech Connect (OSTI)

Quantification of the residual nuclear material remaining in process equipment has long been a challenge to those who work with nuclear material accounting systems. Fortunately, nuclear material has spontaneous radiation emissions that can be measured. If gamma-ray measurements can be made, it is easy to determine what isotope a deposit contains. Unfortunately, it can be quite difficult to relate this measured signal to an estimate of the mass of the nuclear deposit. Typically, the measurement expert must work with incomplete or inadequate information to determine a quantitative result. Simplified analysis models, the distribution of the nuclear material, any intervening attenuation, background(s), and the source-to-detector distance(s) can have significant impacts on the quantitative result. This presentation discusses the application of a generalized-geometry holdup model to the low-enriched uranium fuel pellet fabrication plant in Ust-Kamenogorsk, Kazakhstan. Preliminary results will be presented. Software tools have been developed to assist the facility operators in performing and documenting the measurements. Operator feedback has been used to improve the user interfaces.

Barham, M.A.; Ceo, R.N.; Smith, S.E. [Oak Ridge Y-12 Plant, TN (United States)] [and others

1998-12-31T23:59:59.000Z

56

Candidate processes for diluting the {sup 235}U isotope in weapons-capable highly enriched uranium  

SciTech Connect (OSTI)

The United States Department of Energy (DOE) is evaluating options for rendering its surplus inventories of highly enriched uranium (HEU) incapable of being used to produce nuclear weapons. Weapons-capable HEU was earlier produced by enriching uranium in the fissile {sup 235}U isotope from its natural occurring 0.71 percent isotopic concentration to at least 20 percent isotopic concentration. Now, by diluting its concentration of the fissile {sup 235}U isotope in a uranium blending process, the weapons capability of HEU can be eliminated in a manner that is reversible only through isotope enrichment, and therefore, highly resistant to proliferation. To the extent that can be economically and technically justified, the down-blended uranium product will be made suitable for use as commercial reactor fuel. Such down-blended uranium product can also be disposed of as waste if chemical or isotopic impurities preclude its use as reactor fuel.

Snider, J.D.

1996-02-01T23:59:59.000Z

57

EA-1255: Project Partnership Transportation of Foreign-Owned Enriched Uranium from the Republic of Georgia  

Broader source: Energy.gov [DOE]

This EA evaluates the environmental impacts for the proposal to transport 5.26 kilograms of enriched uranium-23 5 in the form of nuclear fuel, from the Republic of Georgia to the United Kingdom.

59

Criteria for the safe storage of enriched uranium at the Y-12 Plant  

SciTech Connect (OSTI)

Uranium storage practices at US Department of Energy (DOE) facilities have evolved over a period spanning five decades of programmatic work in support of the nuclear deterrent mission. During this period, the Y-12 Plant in Oak Ridge, Tennessee has served as the principal enriched uranium facility for fabrication, chemical processing, metallurgical processing and storage. Recent curtailment of new nuclear weapons production and stockpile reduction has created significant amounts of enriched uranium available as a strategic resource which must be properly and safely stored. This standard specifies criteria associated with the safe storage of enriched uranium at the Y-12 Plant. Because programmatic needs, compliance regulations and desirable materials of construction change with time, it is recommended that these standards be reviewed and amended periodically to ensure that they continue to serve their intended purpose.

Cox, S.O.

1995-07-01T23:59:59.000Z

60

Examination of the conversion of the U.S. submarine fleet from highly enriched uranium to low enriched uranium ; Examination of the conversion of the United States submarine fleet from HEU to low LEU .  

E-Print Network [OSTI]

??The nuclear reactors used by the U.S. Navy for submarine propulsion are currently fueled by highly enriched uranium (HEU), but HEU brings administrative and political… (more)

McCord, Cameron (Cameron Liam)

2014-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


61

Environmental monitoring for detection of uranium enrichment operations: Comparison of LEU and HEU facilities  

SciTech Connect (OSTI)

In 1994, the International Atomic Energy Agency (IAEA) initiated an ambitious program of worldwide field trials to evaluate the utility of environmental monitoring for safeguards. Part of this program involved two extensive United States field trials conducted at the large uranium enrichment facilities. The Paducah operation involves a large low-enriched uranium (LEU) gaseous diffusion plant while the Portsmouth facilities include a large gaseous diffusion plant that has produced both LEU and high-enriched uranium (HEU) as well as an LEU centrifuge facility. As a result of the Energy Policy Act of 1992, management of the uranium enrichment operations was assumed by the US Enrichment Corporation (USEC). The facilities are operated under contract by Martin Marietta Utility Services. Martin Marietta Energy Systems manages the environmental restoration and waste management programs at Portsmouth and Paducah for DOE. These field trials were conducted. Samples included swipes from inside and outside process buildings, vegetation and soil samples taken from locations up to 8 km from main sites, and hydrologic samples taken on the sites and at varying distances from the sites. Analytical results from bulk analysis were obtained using high abundance sensitivity thermal ionization mm spectrometers (TIMS). Uranium isotopics altered from the normal background percentages were found for all the sample types listed above, even on vegetation 5 km from one of the enrichment facilities. The results from these field trials demonstrate that dilution by natural background uranium does not remove from environmental samples the distinctive signatures that are characteristic of enrichment operations. Data from swipe samples taken within the enrichment facilities were particularly revealing. Particulate analysis of these swipes provided a detailed ``history`` of both facilities, including the assays of the end product and tails for both facilities.

Hembree, D.M. Jr.; Carter, J.A.; Ross, H.H.

1995-03-01T23:59:59.000Z

62

Containment and storage of uranium hexafluoride at US Department of Energy uranium enrichment plants  

SciTech Connect (OSTI)

Isotopically depleted UF{sub 6} (uranium hexafluoride) accumulates at a rate five to ten times greater than the enriched product and is stored in steel vessels at the enrichment plant sites. There are approximately 55,000 large cylinders now in storage at Paducah, Kentucky; Portsmouth, Ohio; and Oak Ridge, Tennessee. Most of them contain a nominal 14 tons of depleted UF{sub 6}. Some of these cylinders have been in the unprotected outdoor storage environment for periods approaching 40 years. Storage experience, supplemented by limited corrosion data, suggests a service life of about 70 years under optimum conditions for the 48-in. diameter, 5/16-in.-wall pressure vessels (100 psi working pressure), using a conservative industry-established 1/4-in.-wall thickness as the service limit. In the past few years, however, factors other than atmospheric corrosion have become apparent that adversely affect the serviceability of small numbers of the storage containers and that indicate the need for a managed program to ensure maintenance ofcontainment integrity for all the cylinders in storage. The program includes periodic visual inspections of cylinders and storage yards with documentation for comparison with other inspections, a group of corrosion test programs to permit cylinder life forecasts, and identification of (and scheduling for remedial action) situations in which defects, due to handling damage or accelerated corrosion, can seriously shorten the storage life or compromise the containment integrity of individual cylinders. The program also includes rupture testing to assess the effects of certain classes of damage on overall cylinder strength, aswell as ongoing reviews of specifications, procedures, practices, and inspection results to effect improvements in handling safety, containment integrity, and storage life.

Barlow, C.R.; Alderson, J.H.; Blue, S.C.; Boelens, R.A.; Conkel, M.E.; Dorning, R.E.; Ecklund, C.D.; Halicks, W.G.; Henson, H.M.; Newman, V.S.; Philpot, H.E.; Taylor, M.S.; Vournazos, J.P. [Oak Ridge K-25 Site, TN (United States). UEO Enrichment Technical Operations Div.; Russell, J.R. [USDOE Oak Ridge Field Office, TN (United States); Pryor, W.A. [PAI Corp., Oak Ridge, TN (United States); Ziehlke, K.T. [MJB Technical Associates (United States)

1992-07-01T23:59:59.000Z

63

Compact reaction cell for homogenizing and down-blending highly enriched uranium metal  

DOE Patents [OSTI]

The invention is a specialized reaction cell for converting uranium metal to uranium oxide. In a preferred form, the reaction cell comprises a reaction chamber with increasing diameter along its length (e.g. a cylindrical chamber having a diameter of about 2 inches in a lower portion and having a diameter of from about 4 to about 12 inches in an upper portion). Such dimensions are important to achieve the necessary conversion while at the same time affording criticality control and transportability of the cell and product. The reaction chamber further comprises an upper port and a lower port, the lower port allowing for the entry of reactant gases into the reaction chamber, the upper port allowing for the exit of gases from the reaction chamber. A diffuser plate is attached to the lower port of the reaction chamber and serves to shape the flow of gas into the reaction chamber. The reaction cell further comprises means for introducing gases into the reaction chamber and a heating means capable of heating the contents of the reaction chamber. The present invention also relates to a method for converting uranium metal to uranium oxide in the reaction cell of the present invention. The invention is useful for down-blending highly enriched uranium metal by the simultaneous conversion of highly enriched uranium metal and natural or depleted uranium metal to uranium oxide within the reaction cell. 4 figs.

McLean, W. II; Miller, P.E.; Horton, J.A.

1995-05-02T23:59:59.000Z

64

Compact reaction cell for homogenizing and down-blanding highly enriched uranium metal  

DOE Patents [OSTI]

The invention is a specialized reaction cell for converting uranium metal to uranium oxide. In a preferred form, the reaction cell comprises a reaction chamber with increasing diameter along its length (e.g. a cylindrical chamber having a diameter of about 2 inches in a lower portion and having a diameter of from about 4 to about 12 inches in an upper portion). Such dimensions are important to achieve the necessary conversion while at the same time affording criticality control and transportability of the cell and product. The reaction chamber further comprises an upper port and a lower port, the lower port allowing for the entry of reactant gasses into the reaction chamber, the upper port allowing for the exit of gasses from the reaction chamber. A diffuser plate is attached to the lower port of the reaction chamber and serves to shape the flow of gas into the reaction chamber. The reaction cell further comprises means for introducing gasses into the reaction chamber and a heating means capable of heating the contents of the reaction chamber. The present invention also relates to a method for converting uranium metal to uranium oxide in the reaction cell of the present invention. The invention is useful for down-blending highly enriched uranium metal by the simultaneous conversion of highly enriched uranium metal and natural or depleted uranium metal to uranium oxide within the reaction cell.

McLean, II, William (Oakland, CA); Miller, Philip E. (Livermore, CA); Horton, James A. (Livermore, CA)

1995-01-01T23:59:59.000Z

65

Establishing a Cost Basis for Converting the High Flux Isotope Reactor from High Enriched to Low Enriched Uranium Fuel  

SciTech Connect (OSTI)

Under the auspices of the Global Threat Reduction Initiative Reduced Enrichment for Research and Test Reactors Program, the National Nuclear Security Administration /Department of Energy (NNSA/DOE) has, as a goal, to convert research reactors worldwide from weapons grade to non-weapons grade uranium. The High Flux Isotope Reactor (HFIR) at Oak Ridge National Lab (ORNL) is one of the candidates for conversion of fuel from high enriched uranium (HEU) to low enriched uranium (LEU). A well documented business model, including tasks, costs, and schedules was developed to plan the conversion of HFIR. Using Microsoft Project, a detailed outline of the conversion program was established and consists of LEU fuel design activities, a fresh fuel shipping cask, improvements to the HFIR reactor building, and spent fuel operations. Current-value costs total $76 million dollars, include over 100 subtasks, and will take over 10 years to complete. The model and schedule follows the path of the fuel from receipt from fuel fabricator to delivery to spent fuel storage and illustrates the duration, start, and completion dates of each subtask to be completed. Assumptions that form the basis of the cost estimate have significant impact on cost and schedule.

Primm, Trent [ORNL; Guida, Tracey [University of Pittsburgh

2010-02-01T23:59:59.000Z

66

Material accountancy in the Ningyo-Toge uranium enrichment pilot plant  

SciTech Connect (OSTI)

The uranium enrichment pilot plant at PNC Ningyo-Toge Works, Japan, started operation in August 1979. Since then, inspection activities by the government of Japan and the International Atomic Energy Agency (IAEA) have been carried out. A basic measure of safeguards is evaluation of material unaccounted for (MUF) by closing the material balance. As the plant now produces uranium of <5% enrichment, a material balance is closed only once a year. Until now, eight physical inventories have been taken. This paper describes the operator's procedures for material accountability and the values of MUF reported to the government of Japan and the IAEA.

Akiba, M; Iwamoto, T.; Hori, M.; Ikeda, K.; Tani, A.

1987-01-01T23:59:59.000Z

67

Uranium Enrichment Standards of the Y-12 Nuclear Detection and Sensor Testing Center  

SciTech Connect (OSTI)

The Y-12 National Security Complex has recently fabricated and characterized a new series of metallic uranium standards for use in the Nuclear Detection and Sensor Testing Center (NDSTC). Ten uranium metal disks with enrichments varying from 0.2 to 93.2% {sup 235}U were designed to provide researchers access to a wide variety of measurement scenarios in a single testing venue. Special care was taken in the selection of the enrichments in order to closely bracket the definitions of reactor fuel at 4% {sup 235}U and that of highly enriched uranium (HEU) at 20% {sup 235}U. Each standard is well characterized using analytical chemistry as well as a series of gamma-ray spectrometry measurements. Gamma-ray spectra of these standards are being archived in a reference library for use by customers of the NDSTC. A software database tool has been created that allows for easier access and comparison of various spectra. Information provided through the database includes: raw count data (including background spectra), regions of interest (ROIs), and full width half maximum calculations. Input is being sought from the user community on future needs including enhancements to the spectral database and additional Uranium standards, shielding configurations and detector types. A related presentation are planned for the INMM 53rd Annual Meeting (Hull, et al.), which describe new uranium chemical compound standards and testing opportunities at Y-12 Nuclear Detection and Sensor Testing Center (NDSTC).

Cantrell, J.

2012-05-23T23:59:59.000Z

68

CRAD, Criticality Safety- Y-12 Enriched Uranium Operations Oxide Conversion Facility  

Broader source: Energy.gov [DOE]

A section of Appendix C to DOE G 226.1-2 "Federal Line Management Oversight of Department of Energy Nuclear Facilities." Consists of Criteria Review and Approach Documents (CRADs) used for a January 2005 assessment of the Criticality Safety program at the Y-12 - Enriched Uranium Facility.

69

CRAD, Conduct of Operations- Y-12 Enriched Uranium Operations Oxide Conversion Facility  

Broader source: Energy.gov [DOE]

A section of Appendix C to DOE G 226.1-2 "Federal Line Management Oversight of Department of Energy Nuclear Facilities." Consists of Criteria Review and Approach Documents (CRADs) used for a January, 2005 assessment of Conduct of Operations program at the Y-12 - Enriched Uranium Operations Oxide Conversion Facility.

70

CRAD, Environmental Protection- Y-12 Enriched Uranium Operations Oxide Conversion Facility  

Broader source: Energy.gov [DOE]

A section of Appendix C to DOE G 226.1-2 "Federal Line Management Oversight of Department of Energy Nuclear Facilities." Consists of Criteria Review and Approach Documents (CRADs) used for a January 2005 assessment of Environmental Compliance program at the Y-12 - Enriched Uranium Operations Oxide Conversion Facility.

71

CRAD, Occupational Safety & Health- Y-12 Enriched Uranium Operations Oxide Conversion Facility  

Broader source: Energy.gov [DOE]

A section of Appendix C to DOE G 226.1-2 "Federal Line Management Oversight of Department of Energy Nuclear Facilities." Consists of Criteria Review and Approach Documents (CRADs) used for a January 2005 assessment of Industrial Safety and Industrial Health programs at the Y-12 - Enriched Uranium Operations Oxide Conversion Facility.

72

CRAD, Emergency Management- Y-12 Enriched Uranium Operations Oxide Conversion Facility  

Broader source: Energy.gov [DOE]

A section of Appendix C to DOE G 226.1-2 "Federal Line Management Oversight of Department of Energy Nuclear Facilities." Consists of Criteria Review and Approach Documents (CRADs) used for a January 2005 assessment of Emergency Management program at the Y-12 Enriched Uranium Operations Oxide Conversion Facility.

73

CRAD, Radiological Controls- Y-12 Enriched Uranium Operations Oxide Conversion Facility  

Broader source: Energy.gov [DOE]

A section of Appendix C to DOE G 226.1-2 "Federal Line Management Oversight of Department of Energy Nuclear Facilities." Consists of Criteria Review and Approach Documents (CRADs) used for a January 2005 assessment of the Radiation Protection Program at the Y-12 - Enriched Uranium Operations Oxide Conversion Facility.

74

CRAD, DOE Oversight- Y-12 Enriched Uranium Operations Oxide Conversion Facility  

Broader source: Energy.gov [DOE]

A section of Appendix C to DOE G 226.1-2 "Federal Line Management Oversight of Department of Energy Nuclear Facilities." Consists of Criteria Review and Approach Documents (CRADs) used for a DOE independent oversight assessment of the Y-12 Site Office's programs for oversight of its contractors at the Y-12 Enriched Uranium Operations Oxide Conversion Facility.

75

CRAD, Safety Basis- Y-12 Enriched Uranium Operations Oxide Conversion Facility  

Broader source: Energy.gov [DOE]

A section of Appendix C to DOE G 226.1-2 "Federal Line Management Oversight of Department of Energy Nuclear Facilities." Consists of Criteria Review and Approach Documents (CRADs) used for a January 2005 assessment of the Safety Basis at the Y-12 - Enriched Uranium Operations Oxide Conversion Facility.

76

SciTech Connect: "enriched uranium"  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administrationcontroller systems controller systemsisSchedulesenriched uranium" Find + Advanced

77

Initial report on characterization of excess highly enriched uranium  

SciTech Connect (OSTI)

DOE`s Office of Fissile Materials Disposition assigned to this Y-12 division the task of preparing a report on the 174.4 metric tons of excess highly enriched U. Characterization included identification by category, gathering existing data (assay), defining the likely needed processing steps for prepping for transfer to a blending site, and developing a range of preliminary cost estimates for those steps. Focus is on making commercial reactor fuel as a final disposition path.

NONE

1996-07-01T23:59:59.000Z

78

Continuing investigations for technology assessment of /sup 99/Mo production from LEU (low enriched Uranium) targets  

SciTech Connect (OSTI)

Currently much of the world's supply of /sup 99m/Tc for medical purposes is produced from /sup 99/Mo derived from the fissioning of high enriched uranium (HEU). The need for /sup 99m/Tc is continuing to grow, especially in developing countries, where needs and national priorities call for internal production of /sup 99/Mo. This paper presents the results of our continuing studies on the effects of substituting low enriched Uranium (LEU) for HEU in targets for the production of fission product /sup 99/Mo. Improvements in the electrodeposition of thin films of uranium metal are reported. These improvements continue to increase the appeal for the substitution of LEU metal for HEU oxide films in cylindrical targets. The process is effective for targets fabricated from stainless steel or hastaloy. A cost estimate for setting up the necessary equipment to electrodeposit uranium metal on cylindrical targets is reported. Further investigations on the effect of LEU substitution on processing of these targets are also reported. Substitution of uranium silicides for the uranium-aluminum alloy or uranium aluminide dispersed fuel used in other current target designs will allow the substitution of LEU for HEU in these targets with equivalent /sup 99/Mo-yield per target and no change in target geometries. However, this substitution will require modifications in current processing steps due to (1) the insolubility of uranium silicides in alkaline solutions and (2) the presence of significant quantities of silicate in solution. Results to date suggest that both concerns can be handled and that substitution of LEU for HEU can be achieved.

Vandergrift, G.F.; Kwok, J.D.; Marshall, S.L.; Vissers, D.R.; Matos, J.E.

1987-01-01T23:59:59.000Z

79

Measurement of the enrichment of uranium in the pipework of a gas centrifuge enrichment plant  

SciTech Connect (OSTI)

The US and UK have been separately working on the development of a NDA instrument to determine the enrichment of gaseous UF/sub 6/ at low pressures in cascade header pipework in line with the conclusions of the Hexapartite Safeguards Project viz. the instrument is capable of making a ''go/no go'' decision of whether the enrichment is less than/greater than 20%. Recently, there has been a series of very useful technical exchanges of ideas and information between the two countries. This has led to a technical formulation for such an instrumentation based on ..gamma..-ray spectrometry which, although plant-specific in certain features, nevertheless is based on the same physical principles. Experimental results from commercially operating enrichment plants are very encouraging and indicate that a complete measurement including set up time on the pipe should be attainable in about 30 minutes when measuring pipes of diameter around 110 mm. 5 refs., 4 figs.

Packer, T.W.; Lees, E.W.; Close, D.; Nixon, K.V.; Pratt, J.C.; Strittmatter, R.

1985-01-01T23:59:59.000Z

80

Moderation control in low enriched {sup 235}U uranium hexafluoride packaging operations and transportation  

SciTech Connect (OSTI)

Moderation control is the basic parameter for ensuring nuclear criticality safety during the packaging and transport of low {sup 235}U enriched uranium hexafluoride before its conversion to nuclear power reactor fuel. Moderation control has permitted the shipment of bulk quantities in large cylinders instead of in many smaller cylinders and, therefore, has resulted in economies without compromising safety. Overall safety and uranium accountability have been enhanced through the use of the moderation control. This paper discusses moderation control and the operating procedures to ensure that moderation control is maintained during packaging operations and transportation.

Dyer, R.H. [USDOE Oak Ridge Operations Office, TN (United States); Kovac, F.M. [Oak Ridge National Lab., TN (United States); Pryor, W.A. [PAI Corp., Oak Ridge, TN (United States)

1993-10-01T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


81

Prompt Neutron Decay for Delayed Critical Bare and Natural-Uranium-Reflected Metal Spheres of Plutonium and Highly Enriched Uranium  

SciTech Connect (OSTI)

Prompt neutron decay at delayed criticality was measured by Oak Ridge National Laboratory for uranium-reflected highly enriched uranium (HEU) and Pu metal spheres (FLATTOP), for an unreflected Pu metal (4.5% {sup 240}Pu) sphere (JEZEBEL) at Los Alamos National Laboratory (LANL) and for an unreflected HEU metal sphere at Oak Ridge Critical Experiments Facility. The average prompt neutron decay constants from hundreds of Rossi-{alpha} and randomly pulsed neutron measurements with {sup 252}Cf at delayed criticality are as follows: 3.8458 {+-} 0.0016 x 10{sup 5} s{sup -1}, 2.2139 {+-} 0.0022 x 10{sup 5} s{sup -1}, 6.3126 {+-} 0.0100 x 10{sup 5} s{sup -1}, and 1.1061 {+-} 0.0009 x 10{sup 6} s{sup -1}, respectively. These values agree with previous measurements by LANL for FLATTOP, JEZEBEL, and GODIVA I as follows: 3.82 {+-} 0.02 x 10{sup 5} s{sup -1} for a uranium core; 2.14 {+-} 0.05 x 10{sup 5} s{sup -1} and 2.29 x 10{sup 5} s{sup -1} (uncertainty not reported) for a plutonium core; 6.4 {+-} 0.1 x 10{sup 5} s{sup -1}, and 1.1 {+-} 0.1 x 10{sup 6} s{sup -1}, respectively, but have smaller uncertainties because of the larger number of measurements. For the FLATTOP and JEZEBEL assemblies, the measurements agree with calculations. Traditionally, the calculated decay constants for the bare uranium metal sphere GODIVA I and the Oak Ridge Uranium Metal Sphere were higher than experimental by {approx}10%. Other energy-dependent quantities for the bare uranium sphere agree within 1%.

Mihalczo, John T [ORNL

2011-01-01T23:59:59.000Z

82

Operating limit evaluation for disposal of uranium enrichment plant wastes  

SciTech Connect (OSTI)

A proposed solid waste landfill at Paducah Gaseous Diffusion Plant (PGDP) will accept wastes generated during normal plant operations that are considered to be non-radioactive. However, nearly all solid waste from any source or facility contains small amounts of radioactive material, due to the presence in most materials of trace quantities of such naturally occurring radionuclides as uranium and thorium. This paper describes an evaluation of operating limits, which are protective of public health and the environment, that would allow waste materials containing small amounts of radioactive material to be sent to a new solid waste landfill at PGDP. The operating limits are expressed as limits on concentrations of radionuclides in waste materials that could be sent to the landfill based on a site-specific analysis of the performance of the facility. These limits are advantageous to PGDP and DOE for several reasons. Most importantly, substantial cost savings in the management of waste is achieved. In addition, certain liabilities that could result from shipment of wastes to a commercial off-site solid waste landfill are avoided. Finally, assurance that disposal operations at the PGDP landfill are protective of public health and the environment is provided by establishing verifiable operating limits for small amounts of radioactive material; rather than relying solely on administrative controls. The operating limit determined in this study has been presented to the Commonwealth of Kentucky and accepted as a condition to be attached to the operating permit for the solid waste landfill.

Lee, D.W.; Kocher, D.C.; Wang, J.C.

1996-02-01T23:59:59.000Z

83

Establishing Specifications for Low Enriched Uranium Fuel Operations Conducted Outside the High Flux Isotope Reactor Site  

SciTech Connect (OSTI)

The National Nuclear Security Administration (NNSA) has funded staff at Oak Ridge National Laboratory (ORNL) to study the conversion of the High Flux Isotope Reactor (HFIR) from the current, high enriched uranium fuel to low enriched uranium fuel. The LEU fuel form is a metal alloy that has never been used in HFIR or any HFIR-like reactor. This report provides documentation of a process for the creation of a fuel specification that will meet all applicable regulations and guidelines to which UT-Battelle, LLC (UTB) the operating contractor for ORNL - must adhere. This process will allow UTB to purchase LEU fuel for HFIR and be assured of the quality of the fuel being procured.

Pinkston, Daniel [ORNL; Primm, Trent [ORNL; Renfro, David G [ORNL; Sease, John D [ORNL

2010-10-01T23:59:59.000Z

84

EA-1123: Transfer of Normal and Low-Enriched Uranium Billets to the United Kingdom, Hanford Site, Richland, Washington  

Broader source: Energy.gov [DOE]

This EA evaluates the environmental impacts of the proposal to transfer approximately 710,000 kilograms (1,562,000 pounds) of unneeded normal and low-enriched uranium to the United Kingdom; thus,...

85

The US uranium revitalization, Tailings Reclamation and Enrichment Act, Title 1  

SciTech Connect (OSTI)

On November 4, 1987, the US Senate Committee on Energy and Natural Resources reported out to the Senate bill number S.1846 (Uranium Revitalization, Tailings Reclamation and Enrichment Act of 1987). In early 1988, the bill was reintroduced as S.2097, withut some of its earlier provisions that had caused jurisdictional conflict with the Senate Finance Committee. One of the deleted provisions comprised most of Title I of S.1846, dealing primarily with establishing a fee on the use of imported uranium by US utilities. These provisions were reintroduced by amendment on the floor of the Senate on March 30, 1988. In a key vote, a motion to block the reintroduction of the deleted provisions was defeated by a 47-45 margin. The full bill S.2097, again with uranium import provisions, was subsequently passed by a vote of 62-28 in the Senate. The bill now goes to the US House of Representatives for its consideration.

NONE

1988-05-01T23:59:59.000Z

86

Design Study for a Low-Enriched Uranium Core for the High Flux Isotope Reactor, Annual report for FY 2009  

SciTech Connect (OSTI)

This report documents progress made during FY 2009 in studies of converting the High Flux Isotope Reactor (HFIR) from high enriched uranium (HEU) fuel to low enriched uranium (LEU) fuel. Conversion from HEU to LEU will require a change in fuel form from uranium oxide to a uranium-molybdenum alloy. With axial and radial grading of the fuel foil and an increase in reactor power to 100 MW, calculations indicate that the HFIR can be operated with LEU fuel with no degradation in reactor performance from the current level. Results of selected benchmark studies imply that calculations of LEU performance are accurate. Studies are reported of the application of a silicon coating to surrogates for spheres of uranium-molybdenum alloy. A discussion of difficulties with preparing a fuel specification for the uranium-molybdenum alloy is provided. A description of the progress in developing a finite element thermal hydraulics model of the LEU core is provided.

Chandler, David [ORNL; Freels, James D [ORNL; Ilas, Germina [ORNL; Miller, James Henry [ORNL; Primm, Trent [ORNL; Sease, John D [ORNL; Guida, Tracey [University of Pittsburgh; Jolly, Brian C [ORNL

2010-02-01T23:59:59.000Z

87

Experimental critical parameters of enriched uranium solution in annular tank geometries  

SciTech Connect (OSTI)

A total of 61 critical configurations are reported for experiments involving various combinations of annular tanks into which enriched uranium solution was pumped. These experiments were performed at two widely separated times in the 1980s under two programs at the Rocky Flats Plant`s Critical Mass Laboratory. The uranyl nitrate solution contained about 370 g of uranium per liter, but this concentration varied a little over the duration of the studies. The uranium was enriched to about 93% [sup 235]U. All tanks were typical of sizes commonly found in nuclear production plants. They were about 2 m tall and ranged in diameter from 0.6 m to 1.5 m. Annular thicknesses and conditions of neutron reflection, moderation, and absorption were such that criticality would be achieved with these dimensions. Only 13 of the entire set of 74 experiments proved to be subcritical when tanks were completely filled with solution. Single tanks of several radial thicknesses were studied as well as small line arrays (1 x 2 and 1 x 3) of annular tanks. Many systems were reflected on four sides and the bottom by concrete, but none were reflected from above. Many experiments also contained materials within and outside the annular regions that contained strong neutron absorbers. One program had such a thick external moderator/absorber combination that no reflector was used at all.

Rothe, R.E.

1996-04-01T23:59:59.000Z

88

Minimum mass of moderator required for criticality of homogeneous low-enriched uranium systems  

SciTech Connect (OSTI)

A parametric calculational analysis has been performed in order to estimate the minimum mass of moderator required for criticality of homogeneous low-enriched uranium systems. The analysis was performed using a version of the SCALE-4.0 code system and the 27-group ENDF/B-IV cross-section library. Water-moderated uranyl fluoride (UO[sub 2]F[sub 2] and H[sub 2]O) and hydrofluoric-acid-moderated uranium hexaflouride (UF[sub 6] and HF) systems were considered in the analysis over enrichments of 1.4 to 5 wt % [sup 235]U. Estimates of the minimum critical volume, minimum critical mass of uranium, and the minimum mass of moderator required for criticality are presented. There was significant disagreement between the values generated in this study when compared with a similar undocumented study performed in 1983 using ANISN and the Knight-modified Hansen-Roach cross sections. An investigation into the cause of the disagreement was made, and the results are presented.

Jordan, W.C.; Turner, J.C.

1992-12-01T23:59:59.000Z

89

Minimum mass of moderator required for criticality of homogeneous low-enriched uranium systems  

SciTech Connect (OSTI)

A parametric calculational analysis has been performed in order to estimate the minimum mass of moderator required for criticality of homogeneous low-enriched uranium systems. The analysis was performed using a version of the SCALE-4.0 code system and the 27-group ENDF/B-IV cross-section library. Water-moderated uranyl fluoride (UO{sub 2}F{sub 2} and H{sub 2}O) and hydrofluoric-acid-moderated uranium hexaflouride (UF{sub 6} and HF) systems were considered in the analysis over enrichments of 1.4 to 5 wt % {sup 235}U. Estimates of the minimum critical volume, minimum critical mass of uranium, and the minimum mass of moderator required for criticality are presented. There was significant disagreement between the values generated in this study when compared with a similar undocumented study performed in 1983 using ANISN and the Knight-modified Hansen-Roach cross sections. An investigation into the cause of the disagreement was made, and the results are presented.

Jordan, W.C.; Turner, J.C.

1992-12-01T23:59:59.000Z

90

DESIGN STUDY FOR A LOW-ENRICHED URANIUM CORE FOR THE HIGH FLUX ISOTOPE REACTOR, ANNUAL REPORT FOR FY 2010  

SciTech Connect (OSTI)

This report documents progress made during FY 2010 in studies of converting the High Flux Isotope Reactor (HFIR) from high enriched uranium (HEU) fuel to low enriched uranium (LEU) fuel. Conversion from HEU to LEU will require a change in fuel form from uranium oxide to a uranium-molybdenum alloy. With axial and radial grading of the fuel foil and an increase in reactor power to 100 MW, calculations indicate that the HFIR can be operated with LEU fuel with no degradation in performance to users from the current level. Studies are reported of support to a thermal hydraulic test loop design, the implementation of finite element, thermal hydraulic analysis capability, and infrastructure tasks at HFIR to upgrade the facility for operation at 100 MW. A discussion of difficulties with preparing a fuel specification for the uranium-molybdenum alloy is provided. Continuing development in the definition of the fuel fabrication process is described.

Cook, David Howard [ORNL; Freels, James D [ORNL; Ilas, Germina [ORNL; Jolly, Brian C [ORNL; Miller, James Henry [ORNL; Primm, Trent [ORNL; Renfro, David G [ORNL; Sease, John D [ORNL; Pinkston, Daniel [ORNL

2011-02-01T23:59:59.000Z

91

Validation of the Monte Carlo Criticality Program KENO V. a for highly-enriched uranium systems  

SciTech Connect (OSTI)

A series of calculations based on critical experiments have been performed using the KENO V.a Monte Carlo Criticality Program for the purpose of validating KENO V.a for use in evaluating Y-12 Plant criticality problems. The experiments were reflected and unreflected systems of single units and arrays containing highly enriched uranium metal or uranium compounds. Various geometrical shapes were used in the experiments. The SCALE control module CSAS25 with the 27-group ENDF/B-4 cross-section library was used to perform the calculations. Some of the experiments were also calculated using the 16-group Hansen-Roach Library. Results are presented in a series of tables and discussed. Results show that the criteria established for the safe application of the KENO IV program may also be used for KENO V.a results.

Knight, J.R.

1984-11-01T23:59:59.000Z

92

ZPR-3 Assembly 6F : A spherical assembly of highly enriched uranium, depleted uranium, aluminum and steel with an average {sup 235}U enrichment of 47 atom %.  

SciTech Connect (OSTI)

Over a period of 30 years, more than a hundred Zero Power Reactor (ZPR) critical assemblies were constructed at Argonne National Laboratory. The ZPR facilities, ZPR-3, ZPR-6, ZPR-9 and ZPPR, were all fast critical assembly facilities. The ZPR critical assemblies were constructed to support fast reactor development, but data from some of these assemblies are also well suited for nuclear data validation and to form the basis for criticality safety benchmarks. A number of the Argonne ZPR/ZPPR critical assemblies have been evaluated as ICSBEP and IRPhEP benchmarks. Of the three classes of ZPR assemblies, engineering mockups, engineering benchmarks and physics benchmarks, the last group tends to be most useful for criticality safety. Because physics benchmarks were designed to test fast reactor physics data and methods, they were as simple as possible in geometry and composition. The principal fissile species was {sup 235}U or {sup 239}Pu. Fuel enrichments ranged from 9% to 95%. Often there were only one or two main core diluent materials, such as aluminum, graphite, iron, sodium or stainless steel. The cores were reflected (and insulated from room return effects) by one or two layers of materials such as depleted uranium, lead or stainless steel. Despite their more complex nature, a small number of assemblies from the other two classes would make useful criticality safety benchmarks because they have features related to criticality safety issues, such as reflection by soil-like material. ZPR-3 Assembly 6 consisted of six phases, A through F. In each phase a critical configuration was constructed to simulate a very simple shape such as a slab, cylinder or sphere that could be analyzed with the limited analytical tools available in the 1950s. In each case the configuration consisted of a core region of metal plates surrounded by a thick depleted uranium metal reflector. The average compositions of the core configurations were essentially identical in phases A - F. ZPR-3 Assembly 6F (ZPR-3/6F), the final phase of the Assembly 6 program, simulated a spherical core with a thick depleted uranium reflector. ZPR-3/6F was designed as a fast reactor physics benchmark experiment with an average core {sup 235}U enrichment of approximately 47 at.%. Approximately 81.4% of the total fissions in this assembly occur above 100 keV, approximately 18.6% occur below 100 keV, and essentially none below 0.625 eV - thus the classification as a 'fast' assembly. This assembly is Fast Reactor Benchmark No. 7 in the Cross Section Evaluation Working Group (CSEWG) Benchmark Specifications and has historically been used as a data validation benchmark assembly. Loading of ZPR-3/6F began in late December 1956, and the experimental measurements were performed in January 1957. The core consisted of highly enriched uranium (HEU) plates, depleted uranium plates, perforated aluminum plates and stainless steel plates loaded into aluminum drawers, which were inserted into the central square stainless steel tubes of a 31 x 31 matrix on a split table machine. The core unit cell consisted of three columns of 0.125 in.-wide (3.175 mm) HEU plates, three columns of 0.125 in.-wide depleted uranium plates, nine columns of 0.125 in.-wide perforated aluminum plates and one column of stainless steel plates. The maximum length of each column of core material in a drawer was 9 in. (228.6 mm). Because of the goal to produce an approximately spherical core, core fuel and diluent column lengths generally varied between adjacent drawers and frequently within an individual drawer. The axial reflector consisted of depleted uranium plates and blocks loaded in the available space in the front (core) drawers, with the remainder loaded into back drawers behind the front drawers. The radial reflector consisted of blocks of depleted uranium loaded directly into the matrix tubes. The assembly geometry approximated a reflected sphere as closely as the square matrix tubes, the drawers and the shapes of fuel and diluent plates allowed. According to the logbook and loading records for ZPR-3/6F

Lell, R. M.; McKnight, R. D; Schaefer, R. W.; Nuclear Engineering Division

2010-09-30T23:59:59.000Z

93

CONCEPTUAL PROCESS DESCRIPTION FOR THE MANUFACTURE OF LOW-ENRICHED URANIUM-MOLYBDENUM FUEL  

SciTech Connect (OSTI)

The National Nuclear Security Agency Global Threat Reduction Initiative (GTRI) is tasked with minimizing the use of high-enriched uranium (HEU) worldwide. A key component of that effort is the conversion of research reactors from HEU to low-enriched uranium (LEU) fuels. The GTRI Convert Fuel Development program, previously known as the Reduced Enrichment for Research and Test Reactors program was initiated in 1978 by the United States Department of Energy to develop the nuclear fuels necessary to enable these conversions. The program cooperates with the research reactors’ operators to achieve this goal of HEU to LEU conversion without reduction in reactor performance. The programmatic mandate is to complete the conversion of all civilian domestic research reactors by 2014. These reactors include the five domestic high-performance research reactors (HPRR), namely: the High Flux Isotope Reactor at the Oak Ridge National Laboratory, the Advanced Test Reactor at the Idaho National Laboratory, the National Bureau of Standards Reactor at the National Institute of Standards and Technology, the Missouri University Research Reactor at the University of Missouri–Columbia, and the MIT Reactor-II at the Massachusetts Institute of Technology. Characteristics for each of the HPRRs are given in Appendix A. The GTRI Convert Fuel Development program is currently engaged in the development of a novel nuclear fuel that will enable these conversions. The fuel design is based on a monolithic fuel meat (made from a uranium-molybdenum alloy) clad in Al-6061 that has shown excellent performance in irradiation testing. The unique aspects of the fuel design, however, necessitate the development and implementation of new fabrication techniques and, thus, establishment of the infrastructure to ensure adequate fuel fabrication capability. A conceptual fabrication process description and rough estimates of the total facility throughput are described in this document as a basis for establishing preconceptual fabrication facility designs.

Daniel M. Wachs; Curtis R. Clark; Randall J. Dunavant

2008-02-01T23:59:59.000Z

94

Disposition of highly enriched uranium obtained from the Republic of Kazakhstan. Environmental assessment  

SciTech Connect (OSTI)

This EA assesses the potential environmental impacts associated with DOE`s proposal to transport 600 kg of Kazakhstand-origin HEU from Y-12 to a blending site (B&W Lynchburg or NFS Erwin), transport low-enriched UF6 blending stock from a gaseous diffusion plant to GE Wilmington and U oxide blending stock to the blending site, blending the HEU and uranium oxide blending stock to produce LEU in the form of uranyl nitrate, and transport the uranyl nitrate from the blending site to USEC Portsmouth.

NONE

1995-05-01T23:59:59.000Z

95

Process for producing enriched uranium having a {sup 235}U content of at least 4 wt. % via combination of a gaseous diffusion process and an atomic vapor laser isotope separation process to eliminate uranium hexafluoride tails storage  

DOE Patents [OSTI]

An uranium enrichment process capable of producing an enriched uranium, having a {sup 235}U content greater than about 4 wt. %, is disclosed which will consume less energy and produce metallic uranium tails having a lower {sup 235}U content than the tails normally produced in a gaseous diffusion separation process and, therefore, eliminate UF{sub 6} tails storage and sharply reduce fluorine use. The uranium enrichment process comprises feeding metallic uranium into an atomic vapor laser isotope separation process to produce an enriched metallic uranium isotopic mixture having a {sup 235} U content of at least about 2 wt. % and a metallic uranium residue containing from about 0.1 wt. % to about 0.2 wt. % {sup 235} U; fluorinating this enriched metallic uranium isotopic mixture to form UF{sub 6}; processing the resultant isotopic mixture of UF{sub 6} in a gaseous diffusion process to produce a final enriched uranium product having a {sup 235}U content of at least 4 wt. %, and up to 93.5 wt. % or higher, of the total uranium content of the product, and a low {sup 235}U content UF{sub 6} having a {sup 235}U content of about 0.71 wt. % of the total uranium content of the low {sup 235}U content UF{sub 6}; and converting this low {sup 235}U content UF{sub 6} to metallic uranium for recycle to the atomic vapor laser isotope separation process. 4 figs.

Horton, J.A.; Hayden, H.W. Jr.

1995-05-30T23:59:59.000Z

96

Process for producing enriched uranium having a .sup.235 U content of at least 4 wt. % via combination of a gaseous diffusion process and an atomic vapor laser isotope separation process to eliminate uranium hexafluoride tails storage  

DOE Patents [OSTI]

An uranium enrichment process capable of producing an enriched uranium, having a .sup.235 U content greater than about 4 wt. %, is disclosed which will consume less energy and produce metallic uranium tails having a lower .sup.235 U content than the tails normally produced in a gaseous diffusion separation process and, therefore, eliminate UF.sub.6 tails storage and sharply reduce fluorine use. The uranium enrichment process comprises feeding metallic uranium into an atomic vapor laser isotope separation process to produce an enriched metallic uranium isotopic mixture having a .sup.235 U content of at least about 2 wt. % and a metallic uranium residue containing from about 0.1 wt. % to about 0.2 wt. % .sup.235 U; fluorinating this enriched metallic uranium isotopic mixture to form UF.sub.6 ; processing the resultant isotopic mixture of UF.sub.6 in a gaseous diffusion process to produce a final enriched uranium product having a .sup.235 U content of at least 4 wt. %, and up to 93.5 wt. % or higher, of the total uranium content of the product, and a low .sup.235 U content UF.sub.6 having a .sup.235 U content of about 0.71 wt. % of the total uranium content of the low .sup.235 U content UF.sub.6 ; and converting this low .sup.235 U content UF.sub.6 to metallic uranium for recycle to the atomic vapor laser isotope separation process.

Horton, James A. (Livermore, CA); Hayden, Jr., Howard W. (Oakridge, TN)

1995-01-01T23:59:59.000Z

97

Using low-enriched uranium in research reactors: The RERTR program  

SciTech Connect (OSTI)

The goal of the RERTR program is to minimize and eventually eliminate use of highway enriched uranium (HEU) in research and test reactors. The program has been very successful, and has developed low-enriched uranium (LEU) fuel materials and designs which can be used effectively in approximately 90 percent of the research and test reactors which used HEU when the program began. This progress would not have been possible without active international cooperation among fuel developers, commercial vendors, and reactor operators. The new tasks which the RERTR program is undertaking at this time include development of new and better fuels that will allow use of LEU fuels in all research and test reactors; cooperation with Russian laboratories, which will make it possible to minimize and eventually eliminate use of HEU in research reactors throughout the world, irrespective of its origin; and development of an LEU-based process for the production of {sup 99}Mo. Continuation and intensification of international cooperation are essential to the achievement of the ultimate goals of the RERTR program.

Travelli, A.

1994-05-01T23:59:59.000Z

98

ZPR-3 Assembly 12 : A cylindrical assembly of highly enriched uranium, depleted uranium and graphite with an average {sup 235}U enrichment of 21 atom %.  

SciTech Connect (OSTI)

Over a period of 30 years, more than a hundred Zero Power Reactor (ZPR) critical assemblies were constructed at Argonne National Laboratory. The ZPR facilities, ZPR-3, ZPR-6, ZPR-9 and ZPPR, were all fast critical assembly facilities. The ZPR critical assemblies were constructed to support fast reactor development, but data from some of these assemblies are also well suited for nuclear data validation and to form the basis for criticality safety benchmarks. A number of the Argonne ZPR/ZPPR critical assemblies have been evaluated as ICSBEP and IRPhEP benchmarks. Of the three classes of ZPR assemblies, engineering mockups, engineering benchmarks and physics benchmarks, the last group tends to be most useful for criticality safety. Because physics benchmarks were designed to test fast reactor physics data and methods, they were as simple as possible in geometry and composition. The principal fissile species was {sup 235}U or {sup 239}Pu. Fuel enrichments ranged from 9% to 95%. Often there were only one or two main core diluent materials, such as aluminum, graphite, iron, sodium or stainless steel. The cores were reflected (and insulated from room return effects) by one or two layers of materials such as depleted uranium, lead or stainless steel. Despite their more complex nature, a small number of assemblies from the other two classes would make useful criticality safety benchmarks because they have features related to criticality safety issues, such as reflection by soil-like material. ZPR-3 Assembly 12 (ZPR-3/12) was designed as a fast reactor physics benchmark experiment with an average core {sup 235}U enrichment of approximately 21 at.%. Approximately 68.9% of the total fissions in this assembly occur above 100 keV, approximately 31.1% occur below 100 keV, and essentially none below 0.625 eV - thus the classification as a 'fast' assembly. This assembly is Fast Reactor Benchmark No. 9 in the Cross Section Evaluation Working Group (CSEWG) Benchmark Specifications and has historically been used as a data validation benchmark assembly. Loading of ZPR-3 Assembly 12 began in late Jan. 1958, and the Assembly 12 program ended in Feb. 1958. The core consisted of highly enriched uranium (HEU) plates, depleted uranium plates and graphite plates loaded into stainless steel drawers which were inserted into the central square stainless steel tubes of a 31 x 31 matrix on a split table machine. The core unit cell consisted of two columns of 0.125 in.-wide (3.175 mm) HEU plates, seven columns of 0.125 in.-wide depleted uranium plates and seven columns of 0.125 in.-wide graphite plates. The length of each column was 9 in. (228.6 mm) in each half of the core. The graphite plates were included to produce a softer neutron spectrum that would be more characteristic of a large power reactor. The axial blanket consisted of 12 in. (304.8 mm) of depleted uranium behind the core. The thickness of the radial blanket was approximately 12 in. and the length of the radial blanket in each half of the matrix was 21 in. (533.4 mm). The assembly geometry approximated a right circular cylinder as closely as the square matrix tubes allowed. According to the logbook and loading records for ZPR-3/12, the reference critical configuration was loading 10 which was critical on Feb. 5, 1958. The subsequent loadings were very similar but less clean for criticality because there were modifications made to accommodate reactor physics measurements other than criticality. Accordingly, ZPR-3/12 loading 10 was selected as the only configuration for this benchmark. As documented below, it was determined to be acceptable as a criticality safety benchmark experiment. An accurate transformation to a simplified model is needed to make any ZPR assembly a practical criticality-safety benchmark. There is simply too much geometric detail in an exact (as-built) model of a ZPR assembly, even a clean core such as ZPR-3/12 loading 10. The transformation must reduce the detail to a practical level without masking any of the important features of the critical experiment. And it must d

Lell, R. M.; McKnight, R. D.; Perel, R. L.; Wagschal, J. J.; Nuclear Engineering Division; Racah Inst. of Physics

2010-09-30T23:59:59.000Z

99

RADIO FREQUENCY IDENTIFICATION DEVICES: EFFECTIVENESS IN IMPROVING SAFEGUARDS AT GAS-CENTRIFUGE URANIUM-ENRICHMENT PLANTS.  

SciTech Connect (OSTI)

Recent advances in radio frequency identification devices (RFIDs) have engendered a growing interest among international safeguards experts. Potentially, RFIDs could reduce inspection work, viz. the number of inspections, number of samples, and duration of the visits, and thus improve the efficiency and effectiveness of international safeguards. This study systematically examined the applications of RFIDs for IAEA safeguards at large gas-centrifuge enrichment plants (GCEPs). These analyses are expected to help identify the requirements and desirable properties for RFIDs, to provide insights into which vulnerabilities matter most, and help formulate the required assurance tests. This work, specifically assesses the application of RFIDs for the ''Option 4'' safeguards approach, proposed by Bruce Moran, U. S. Nuclear Regulatory Commission (NRC), for large gas-centrifuge uranium-enrichment plants. The features of ''Option 4'' safeguards include placing RFIDs on all feed, product and tails (F/P/T) cylinders, along with WID readers in all FP/T stations and accountability scales. Other features of Moran's ''Option 4'' are Mailbox declarations, monitoring of load-cell-based weighing systems at the F/P/T stations and accountability scales, and continuous enrichment monitors. Relevant diversion paths were explored to evaluate how RFIDs improve the efficiency and effectiveness of safeguards. Additionally, the analysis addresses the use of RFIDs in conjunction with video monitoring and neutron detectors in a perimeter-monitoring approach to show that RFIDs can help to detect unidentified cylinders.

JOE,J.

2007-07-08T23:59:59.000Z

100

Signatures and Methods for the Automated Nondestructive Assay of UF6 Cylinders at Uranium Enrichment Plants  

SciTech Connect (OSTI)

International Atomic Energy Agency (IAEA) inspectors currently perform periodic inspections at uranium enrichment plants to verify UF6 cylinder enrichment declarations. Measurements are typically performed with handheld high-resolution sensors on a sampling of cylinders taken to be representative of the facility’s entire cylinder inventory. These measurements are time-consuming, expensive, and assay only a small fraction of the total cylinder volume. An automated nondestructive assay system capable of providing enrichment measurements over the full volume of the cylinder could improve upon current verification practices in terms of manpower and assay accuracy. Such a station would use sensors that can be operated in an unattended mode at an industrial facility: medium-resolution scintillators for gamma-ray spectroscopy (e.g., NaI(Tl)) and moderated He-3 neutron detectors. This sensor combination allows the exploitation of additional, more-penetrating signatures beyond the traditional 185-keV emission from U-235: neutrons produced from F-19(?,n) reactions (spawned primarily from U 234 alpha emission) and high-energy gamma rays (extending up to 8 MeV) induced by neutrons interacting in the steel cylinder. This paper describes a study of these non-traditional signatures for the purposes of cylinder enrichment verification. The signatures and the radiation sensors designed to collect them are described, as are proof-of-principle cylinder measurements and analyses. Key sources of systematic uncertainty in the non-traditional signatures are discussed, and the potential benefits of utilizing these non-traditional signatures, in concert with an automated form of the traditional 185-keV-based assay, are discussed.

Smith, Leon E.; Mace, Emily K.; Misner, Alex C.; Shaver, Mark W.

2010-08-08T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
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to obtain the most current and comprehensive results.


101

BLENDING LOW ENRICHED URANIUM WITH DEPLETED URANIUM TO CREATE A SOURCE MATERIAL ORE THAT CAN BE PROCESSED FOR THE RECOVERY OF YELLOWCAKE AT A CONVENTIONAL URANIUM MILL  

SciTech Connect (OSTI)

Throughout the United States Department of Energy (DOE) complex, there are a number of streams of low enriched uranium (LEU) that contain various trace contaminants. These surplus nuclear materials require processing in order to meet commercial fuel cycle specifications. To date, they have not been designated as waste for disposal at the DOE's Nevada Test Site (NTS). Currently, with no commercial outlet available, the DOE is evaluating treatment and disposal as the ultimate disposition path for these materials. This paper will describe an innovative program that will provide a solution to DOE that will allow disposition of these materials at a cost that will be competitive with treatment and disposal at the NTS, while at the same time recycling the material to recover a valuable energy resource (yellowcake) for reintroduction into the commercial nuclear fuel cycle. International Uranium (USA) Corporation (IUSA) and Nuclear Fuel Services, Inc. (NFS) have entered into a commercial relationship to pursue the development of this program. The program involves the design of a process and construction of a plant at NFS' site in Erwin, Tennessee, for the blending of contaminated LEU with depleted uranium (DU) to produce a uranium source material ore (USM Ore{trademark}). The USM Ore{trademark} will then be further processed at IUC's White Mesa Mill, located near Blanding, Utah, to produce conventional yellowcake, which can be delivered to conversion facilities, in the same manner as yellowcake that is produced from natural ores or other alternate feed materials. The primary source of feed for the business will be the significant sources of trace contaminated materials within the DOE complex. NFS has developed a dry blending process (DRYSM Process) to blend the surplus LEU material with DU at its Part 70 licensed facility, to produce USM Ore{trademark} with a U235 content within the range of U235 concentrations for source material. By reducing the U235 content to source material levels in this manner, the material will be suitable for processing at a conventional uranium mill under its existing Part 40 license to remove contaminants and enable the product to re-enter the commercial fuel cycle. The tailings from processing the USM Ore{trademark} at the mill will be permanently disposed of in the mill's tailings impoundment as 11e.(2) byproduct material. Blending LEU with DU to make a uranium source material ore that can be returned to the nuclear fuel cycle for processing to produce yellowcake, has never been accomplished before. This program will allow DOE to disposition its surplus LEU and DU in a cost effective manner, and at the same time provide for the recovery of valuable energy resources that would be lost through processing and disposal of the materials. This paper will discuss the nature of the surplus LEU and DU materials, the manner in which the LEU will be blended with DU to form a uranium source material ore, and the legal means by which this blending can be accomplished at a facility licensed under 10 CFR Part 70 to produce ore that can be processed at a conventional uranium mill licensed under 10 CFR Part 40.

Schutt, Stephen M.; Hochstein, Ron F.; Frydenlund, David C.; Thompson, Anthony J.

2003-02-27T23:59:59.000Z

102

Natural phenomena hazards evaluation of equipment and piping of Gaseous Diffusion Plant Uranium Enrichment Facility  

SciTech Connect (OSTI)

In support of the Gaseous Diffusion Plant Safety Analysis Report Upgrade program (GDP SARUP), a natural phenomena hazards evaluation was performed for the main process equipment and piping in the uranium enrichment buildings at Paducah and Portsmouth gaseous diffusion plants. In order to reduce the cost of rigorous analyses, the evaluation methodology utilized a graded approach based on an experience data base collected by SQUG/EPRI that contains information on the performance of industrial equipment and piping during past earthquakes. This method consisted of a screening walkthrough of the facility in combination with the use of engineering judgment and simple calculations. By using these screenings combined with evaluations that contain decreasing conservatism, reductions in the time and cost of the analyses were significant. A team of experienced seismic engineers who were trained in the use of the DOE SQUG/EPRI Walkdown Screening Material was essential to the success of this natural phenomena hazards evaluation.

Singhal, M.K.; Kincaid, J.H.; Hammond, C.R.; Stockdale, B.I.; Walls, J.C. [Oak Ridge National Lab., TN (United States). Technical Programs and Services; Brock, W.R.; Denton, D.R. [Lockheed Martin Energy Systems, Inc., Oak Ridge, TN (United States)

1995-12-31T23:59:59.000Z

103

RUSSIAN-ORIGIN HIGHLY ENRICHED URANIUM SPENT NUCLEAR FUEL SHIPMENT FROM BULGARIA  

SciTech Connect (OSTI)

In July 2008, the Global Threat Reduction Initiative and the IRT 2000 research reactor in Sofia, Bulgaria, operated by the Institute for Nuclear Research and Nuclear Energy (INRNE), safely shipped 6.4 kilograms of Russian origin highly enriched uranium (HEU) spent nuclear fuel (SNF) to the Russian Federation. The shipment, which resulted in the removal of all HEU from Bulgaria, was conducted by truck, barge, and rail modes of transport across two transit countries before reaching the final destination at the Production Association Mayak facility in Chelyabinsk, Russia. This paper describes the work, equipment, organizations, and approvals that were required to complete the spent fuel shipment and provides lessons learned that might assist other research reactor operators with their own spent nuclear fuel shipments.

Kelly Cummins; Igor Bolshinsky; Ken Allen; Tihomir Apostolov; Ivaylo Dimitrov

2009-07-01T23:59:59.000Z

104

Enrichment of specific protozoan populations during in situ bioremediation of uranium-contaminated groundwater  

SciTech Connect (OSTI)

The importance of bacteria in the anaerobic bioremediation of groundwater polluted with organic and/or metal contaminants is well-recognized and in some instances so well understood that modeling of the in situ metabolic activity of the relevant subsurface microorganisms in response to changes in subsurface geochemistry is feasible. However, a potentially significant factor influencing bacterial growth and activity in the subsurface that has not been adequately addressed is protozoan predation of the microorganisms responsible for bioremediation. In field experiments at a uranium-contaminated aquifer located in Rifle, CO, acetate amendments initially promoted the growth of metal-reducing Geobacter species followed by the growth of sulfate-reducers, as previously observed. Analysis of 18S rRNA gene sequences revealed a broad diversity of sequences closely related to known bacteriovorous protozoa in the groundwater prior to the addition of acetate. The bloom of Geobacter species was accompanied by a specific enrichment of sequences most closely related to the amoeboid flagellate, Breviata anathema, which at their peak accounted for over 80% of the sequences recovered. The abundance of Geobacter species declined following the rapid emergence of B. anathema. The subsequent growth of sulfate-reducing Peptococcaceae was accompanied by another specific enrichment of protozoa, but with sequences most similar to diplomonadid flagellates from the family Hexamitidae, which accounted for up to 100% of the sequences recovered during this phase of the bioremediation. These results suggest a prey-predator response with specific protozoa responding to increased availability of preferred prey bacteria. Thus, quantifying the influence of protozoan predation on the growth, activity, and composition of the subsurface bacterial community is essential for predictive modeling of in situ uranium bioremediation strategies.

Holmes, Dawn; Giloteaux, L.; Williams, Kenneth H.; Wrighton, Kelly C.; Wilkins, Michael J.; Thompson, Courtney A.; Roper, Thomas J.; Long, Philip E.; Lovley, Derek

2013-07-28T23:59:59.000Z

105

Development of a core design optimization tool and analysis in support of the planned LEU conversion of the MIT Research Reactor (MITR-II) ; Development of a core design optimization tool and analysis in support of the planned low enriched uranium conversion of the MIT Research Reactor (MITR-II) .  

E-Print Network [OSTI]

??The MIT Research Reactor (MITR-II) is currently undergoing analysis for the planned conversion from high enriched uranium (HEU) to low enriched uranium (LEU), as part… (more)

Connaway, Heather M. (Heather Moira)

2012-01-01T23:59:59.000Z

106

Validity of Hansen-Roach cross sections in low-enriched uranium systems  

SciTech Connect (OSTI)

Within the nuclear criticality safety community, the Hansen-Roach 16 group cross section set has been the standard'' for use in k{sub eff} calculations over the past 30 years. Yet even with its widespread acceptance, there are still questions about its validity and adequacy, about the proper procedure for calculating the potential scattering cross section, {sigma}{sub p}, for uranium and plutonium, and about the concept of resonance self shielding and its impact on cross sections. This paper attempts to address these questions. It provides a brief background on the Hansen-Roach cross sections. Next is presented a review of resonances in cross sections, self shielding of these resonances, and the use of {sigma}{sub p} to characterize resonance self shielding. Three prescriptions for calculating {sigma}{sub p} are given. Finally, results of several calculations of k{sub eff} on low-enriched uranium systems are provided to confirm the validity of the Hansen-Roach cross sections when applied to such systems.

Busch, R.D. (New Mexico Univ., Albuquerque, NM (United States)); O'Dell, R.D. (Los Alamos National Lab., NM (United States))

1991-01-01T23:59:59.000Z

107

E-Print Network 3.0 - anthropogenic uranium enrichments Sample...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Ecology ; Engineering 99 geology and Ranger 1 open-pit uranium mine in Australia Summary: Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

108

REMOVAL OF SOLIDS FROM HIGHLY ENRICHED URANIUM SOLUTIONS USING THE H-CANYON CENTRIFUGE  

SciTech Connect (OSTI)

Prior to the dissolution of Pu-containing materials in HB-Line, highly enriched uranium (HEU) solutions stored in Tanks 11.1 and 12.2 of H-Canyon must be transferred to provide storage space. The proposed plan is to centrifuge the solutions to remove solids which may present downstream criticality concerns or cause operational problems with the 1st Cycle solvent extraction due to the formation of stable emulsions. An evaluation of the efficiency of the H-Canyon centrifuge concluded that a sufficient amount (> 90%) of the solids in the Tank 11.1 and 12.2 solutions will be removed to prevent any problems. We based this conclusion on the particle size distribution of the solids isolated from samples of the solutions and the calculation of particle settling times in the centrifuge. The particle size distributions were calculated from images generated by scanning electron microscopy (SEM). The mean particle diameters for the distributions were 1-3 {micro}m. A significant fraction (30-50%) of the particles had diameters which were < 1 {micro}m; however, the mass of these solids is insignificant (< 1% of the total solids mass) when compared to particles with larger diameters. It is also probable that the number of submicron particles was overestimated by the software used to generate the particle distribution due to the morphology of the filter paper used to isolate the solids. The settling times calculated for the H-Canyon centrifuge showed that particles with diameters less than 1 to 0.5 {micro}m will not have sufficient time to settle. For this reason, we recommend the use of a gelatin strike to coagulate the submicron particles and facilitate their removal from the solution; although we have no experimental basis to estimate the level of improvement. Incomplete removal of particles with diameters < 1 {micro}m should not cause problems during purification of the HEU in the 1st Cycle solvent extraction. Particles with diameters > 1 {micro}m account for > 99% of the solid mass and will be efficiently removed by the centrifuge; therefore, the formation of emulsions during solvent extraction operations is not an issue. Under the current processing plan, the solutions from Tanks 11.1 and 12.2 will be transferred to the enriched uranium storage (EUS) tank following centrifugation. The solution from Tanks 11.1 and 12.2 may remain in the EUS tank for an extended time prior to purification. The effects of extended storage on the solution were not evaluated as part of this study.

Rudisill, T; Fernando Fondeur, F

2009-01-15T23:59:59.000Z

109

ZPR-3 Assembly 11 : A cylindrical sssembly of highly enriched uranium and depleted uranium with an average {sup 235}U enrichment of 12 atom % and a depleted uranium reflector.  

SciTech Connect (OSTI)

Over a period of 30 years, more than a hundred Zero Power Reactor (ZPR) critical assemblies were constructed at Argonne National Laboratory. The ZPR facilities, ZPR-3, ZPR-6, ZPR-9 and ZPPR, were all fast critical assembly facilities. The ZPR critical assemblies were constructed to support fast reactor development, but data from some of these assemblies are also well suited for nuclear data validation and to form the basis for criticality safety benchmarks. A number of the Argonne ZPR/ZPPR critical assemblies have been evaluated as ICSBEP and IRPhEP benchmarks. Of the three classes of ZPR assemblies, engineering mockups, engineering benchmarks and physics benchmarks, the last group tends to be most useful for criticality safety. Because physics benchmarks were designed to test fast reactor physics data and methods, they were as simple as possible in geometry and composition. The principal fissile species was {sup 235}U or {sup 239}Pu. Fuel enrichments ranged from 9% to 95%. Often there were only one or two main core diluent materials, such as aluminum, graphite, iron, sodium or stainless steel. The cores were reflected (and insulated from room return effects) by one or two layers of materials such as depleted uranium, lead or stainless steel. Despite their more complex nature, a small number of assemblies from the other two classes would make useful criticality safety benchmarks because they have features related to criticality safety issues, such as reflection by soil-like material. ZPR-3 Assembly 11 (ZPR-3/11) was designed as a fast reactor physics benchmark experiment with an average core {sup 235}U enrichment of approximately 12 at.% and a depleted uranium reflector. Approximately 79.7% of the total fissions in this assembly occur above 100 keV, approximately 20.3% occur below 100 keV, and essentially none below 0.625 eV - thus the classification as a 'fast' assembly. This assembly is Fast Reactor Benchmark No. 8 in the Cross Section Evaluation Working Group (CSEWG) Benchmark Specificationsa and has historically been used as a data validation benchmark assembly. Loading of ZPR-3 Assembly 11 began in early January 1958, and the Assembly 11 program ended in late January 1958. The core consisted of highly enriched uranium (HEU) plates and depleted uranium plates loaded into stainless steel drawers, which were inserted into the central square stainless steel tubes of a 31 x 31 matrix on a split table machine. The core unit cell consisted of two columns of 0.125 in.-wide (3.175 mm) HEU plates, six columns of 0.125 in.-wide (3.175 mm) depleted uranium plates and one column of 1.0 in.-wide (25.4 mm) depleted uranium plates. The length of each column was 10 in. (254.0 mm) in each half of the core. The axial blanket consisted of 12 in. (304.8 mm) of depleted uranium behind the core. The thickness of the depleted uranium radial blanket was approximately 14 in. (355.6 mm), and the length of the radial blanket in each half of the matrix was 22 in. (558.8 mm). The assembly geometry approximated a right circular cylinder as closely as the square matrix tubes allowed. According to the logbook and loading records for ZPR-3/11, the reference critical configuration was loading 10 which was critical on January 21, 1958. Subsequent loadings were very similar but less clean for criticality because there were modifications made to accommodate reactor physics measurements other than criticality. Accordingly, ZPR-3/11 loading 10 was selected as the only configuration for this benchmark. As documented below, it was determined to be acceptable as a criticality safety benchmark experiment. A very accurate transformation to a simplified model is needed to make any ZPR assembly a practical criticality-safety benchmark. There is simply too much geometric detail in an exact (as-built) model of a ZPR assembly, even a clean core such as ZPR-3/11 loading 10. The transformation must reduce the detail to a practical level without masking any of the important features of the critical experiment. And it must do this without increasing the total uncertain

Lell, R. M.; McKnight, R. D.; Tsiboulia, A.; Rozhikhin, Y.; National Security; Inst. of Physics and Power Engineering

2010-09-30T23:59:59.000Z

110

Low-Enriched Uranium Fuel Design with Two-Dimensional Grading for the High Flux Isotope Reactor  

SciTech Connect (OSTI)

An engineering design study of the conversion of the High Flux Isotope Reactor (HFIR) from high-enriched uranium (HEU) to low-enriched uranium (LEU) fuel is ongoing at Oak Ridge National Laboratory. The computational models developed during fiscal year 2010 to search for an LEU fuel design that would meet the requirements for the conversion and the results obtained with these models are documented and discussed in this report. Estimates of relevant reactor performance parameters for the LEU fuel core are presented and compared with the corresponding data for the currently operating HEU fuel core. The results obtained indicate that the LEU fuel design would maintain the current performance of the HFIR with respect to the neutron flux to the central target region, reflector, and beam tube locations under the assumption that the operating power for the reactor fueled with LEU can be increased from the current value of 85 MW to 100 MW.

Ilas, Germina [ORNL; Primm, Trent [ORNL

2011-05-01T23:59:59.000Z

111

Safeguards by design - industry engagement for new uranium enrichment facilities in the United States  

SciTech Connect (OSTI)

The United States Department of Energy's (DOE's) Office of Nonproliferation and International Security (NA-24) has initiated a Safeguards by Design (SBD) effort to encourage the incorporation of international (IAEA) safeguards features early in the design phase of a new nuclear facility in order to avoid the need to redesign or retrofit the facility at a later date. The main goals of Safeguards by Design are to (1) make the implementation of international safeguards at new civil nuclear facilities more effective and efficient, (2) avoid costly and time-consuming re-design work or retrofits at such facilities and (3) design such facilities in a way that makes proliferation as technically difficult, as time-consuming, and as detectable as possible. The U.S. Nuclear Regulatory Commission (NRC) has recently hosted efforts to facilitate the use of Safeguards by Design for new uranium enrichment facilities currently being planned for construction in the U.S. While SBD is not a NRC requirement, the NRC is aiding the implementation of SBD by coordinating discussions between DOE's NA-24 and industry's facility design teams. More specifically, during their normal course of licensing discussions the NRC has offered industry the opportunity to engage with NA-24 regarding SBD.

Demuth, Scott F [Los Alamos National Laboratory; Grice, Thomas [NRC; Lockwood, Dunbar [DOE/NA-243

2010-01-01T23:59:59.000Z

112

Fission Yield Measurements from Highly Enriched Uranium Irradiated Inside a Boron Carbide Capsule  

SciTech Connect (OSTI)

A boron carbide capsule was previously designed and tested by Pacific Northwest National Laboratory (PNNL) and Washington State University (WSU) for spectral-tailoring in mixed spectrum reactors. The presented work used this B4C capsule to create a fission product sample from the irradiation of highly enriched uranium (HEU) with a fast fission neutron spectrum. An HEU foil was irradiated inside of the capsule in WSU’s 1 MW TRIGA reactor at full power for 200 min to produce 5.8 × 1013 fissions. After three days of cooling, the sample was shipped to PNNL for radiochemical separations and analysis by gamma and beta spectroscopy. Fission yields for products were calculated from the radiometric measurements and compared to measurements from thermal neutron induced fission (analyzed in parallel with the non-thermal sample at PNNL) and published evaluated fast-pooled and thermal nuclear data. Reactor dosimetry measurements were also completed to fully characterize the neutron spectrum and total fluence of the irradiation.

Metz, Lori A.; Friese, Judah I.; Finn, Erin C.; Greenwood, Lawrence R.; Kephart, Rosara F.; Hines, Corey C.; King, Matthew D.; Henry, Kelley; Wall, Donald E.

2013-05-01T23:59:59.000Z

113

Environmental decontamination  

SciTech Connect (OSTI)

The record of the proceedings of the workshop on environmental decontamination contains twenty-seven presentations. Emphasis is placed upon soil and surface decontamination, the decommissioning of nuclear facilities, and assessments of instrumentation and equipment used in decontamination. (DLS)

Cristy, G.A.; Jernigan, H.C. (eds.)

1981-02-01T23:59:59.000Z

114

Low-Enriched Uranium Fuel Conversion Activities for the High Flux Isotope Reactor, Annual Report for FY 2011  

SciTech Connect (OSTI)

This report describes progress made during FY11 in ORNL activities to support converting the High Flux Isotope Reactor (HFIR) from high-enriched uranium (HEU) fuel to low-enriched uranium (LEU) fuel. Conversion from HEU to LEU will require a change in fuel form from uranium oxide to a uranium-molybdenum (UMo) alloy. With both radial and axial contouring of the fuel foil and an increase in reactor power to 100 MW, calculations indicate that the HFIR can be operated with LEU fuel with no degradation in performance to users from the current levels achieved with HEU fuel. Studies are continuing to demonstrate that the fuel thermal safety margins can be preserved following conversion. Studies are also continuing to update other aspects of the reactor steady state operation and accident response for the effects of fuel conversion. Technical input has been provided to Oregon State University in support of their hydraulic testing program. The HFIR conversion schedule was revised and provided to the GTRI program. In addition to HFIR conversion activities, technical support was provided directly to the Fuel Fabrication Capability program manager.

Renfro, David G [ORNL; Cook, David Howard [ORNL; Freels, James D [ORNL; Griffin, Frederick P [ORNL; Ilas, Germina [ORNL; Sease, John D [ORNL; Chandler, David [ORNL

2012-03-01T23:59:59.000Z

115

Preliminary Evaluation of Alternate Designs for HFIR Low-Enriched Uranium Fuel  

SciTech Connect (OSTI)

Engineering design studies of the feasibility of conversion of the High Flux Isotope Reactor (HFIR) from high-enriched uranium (HEU) to low-enriched uranium (LEU) fuel are ongoing at Oak Ridge National Laboratory (ORNL) as part of an effort sponsored by the U.S. Department of Energy’s Global Threat Reduction Initiative (GTRI)/Reduced Enrichment for Research and Test Reactors (RERTR) program. The fuel type selected by the program for the conversion of the five high-power research reactors in the U.S. that still use HEU fuel is a new U-Mo monolithic fuel. Studies by ORNL have previously indicated that HFIR can be successfully converted using the new fuel provided (1) the reactor power can be increased from 85 MW to 100 MW and (2) the fuel can be fabricated to a specific reference design. Fabrication techniques for the new fuel are under development by the program but are still immature, especially for the “complex” aspects of the HFIR fuel design. In FY 2012, the program underwent a major shift in focus to emphasize developing and qualifying processes for the fabrication of reliable and affordable LEU fuel. In support of this new focus and in an effort to ensure that the HFIR fuel design is as suitable for reliable fabrication as possible, ORNL undertook the present study to propose and evaluate several alternative design features. These features include (1) eliminating the fuel zone axial contouring in the previous reference design by substituting a permanent neutron absorber in the lower unfueled region of all of the fuel plates, (2) relocating the burnable neutron absorber from the fuel plates of the inner fuel element to the side plates of the inner fuel element (the fuel plates of the outer fuel element do not contain a burnable absorber), (3) relocating the fuel zone inside the fuel plate to be centered on the centerline of the depth of the plate, and (4) reshaping the radial contour of the relocated fuel zone to be symmetric about this centerline. The present studies used current analytical tools to evaluate the various alternate designs for cycle length, scientific performance (e.g., neutron scattering), and steady-state and transient thermal performance using both safety limit and nominal parameter assumptions. The studies concluded that a new reference design combining a permanent absorber in the lower unfueled region of all of the fuel plates, a burnable absorber in the inner element side plates, and a relocated and reshaped (but still radially contoured) fuel zone will allow successful conversion of HFIR. Future collaboration with the program will reveal whether the new reference design can be fabricated reliably and affordably. Following this feedback, additional studies using state-of-the-art developmental analytical tools are proposed to optimize the design of the fuel zone radial contour and the amount and location of both types of neutron absorbers to further flatten thermal peaks while maximizing the performance of the reactor.

Renfro, David [ORNL; Chandler, David [ORNL; Cook, David [ORNL; Ilas, Germina [ORNL; Jain, Prashant [ORNL; Valentine, Jennifer [ORNL

2014-10-30T23:59:59.000Z

116

Design Study for a Low-Enriched Uranium Core for the High Flux Isotope Reactor, Annual Report for FY 2006  

SciTech Connect (OSTI)

Neutronics and thermal-hydraulics studies show that, for equivalent operating power [85 MW(t)], a low-enriched uranium (LEU) fuel cycle based on uranium-10 wt % molybdenum (U-10Mo) metal foil with radially, “continuously graded” fuel meat thickness results in a 15% reduction in peak thermal flux in the beryllium reflector of the High Flux Isotope Reactor (HFIR) as compared to the current highly enriched uranium (HEU) cycle. The uranium-235 content of the LEU core is almost twice the amount of the HEU core when the length of the fuel cycle is kept the same for both fuels. Because the uranium-238 content of an LEU core is a factor of 4 greater than the uranium-235 content, the LEU HFIR core would weigh 30% more than the HEU core. A minimum U-10Mo foil thickness of 84 ?m is required to compensate for power peaking in the LEU core although this value could be increased significantly without much penalty. The maximum U-10Mo foil thickness is 457?m. Annual plutonium production from fueling the HFIR with LEU is predicted to be 2 kg. For dispersion fuels, the operating power for HFIR would be reduced considerably below 85 MW due to thermal considerations and due to the requirement of a 26-d fuel cycle. If an acceptable fuel can be developed, it is estimated that $140 M would be required to implement the conversion of the HFIR site at Oak Ridge National Laboratory from an HEU fuel cycle to an LEU fuel cycle. To complete the conversion by fiscal year 2014 would require that all fuel development and qualification be completed by the end of fiscal year 2009. Technological development areas that could increase the operating power of HFIR are identified as areas for study in the future.

Primm, R. T. [ORNL] [ORNL; Ellis, R. J. [ORNL] [ORNL; Gehin, J. C. [ORNL] [ORNL; Clarno, K. T. [ORNL] [ORNL; Williams, K. A. [ORNL] [ORNL; Moses, D. L. [ORNL] [ORNL

2006-11-01T23:59:59.000Z

117

NUCLEAR ISOTOPIC DILUTION OF HIGHLY ENRICHED URANIUM BY DRY BLENDING VIA THE RM-2 MILL TECHNOLOGY  

SciTech Connect (OSTI)

DOE has initiated numerous activities to focus on identifying material management strategies to disposition various excess fissile materials. In particular the INEEL has stored 1,700 Kg of offspec HEU at INTEC in CPP-651 vault facility. Currently, the proposed strategies for dispositioning are (a) aqueous dissolution and down blending to LEU via facilities at SRS followed by shipment of the liquid LEU to NFS for fabrication into LWR fuel for the TVA reactors and (b) dilution of the HEU to 0.9% for discard as a waste stream that would no longer have a criticality or proliferation risk without being processed through some type of enrichment system. Dispositioning this inventory as a waste stream via aqueous processing at SRS has been determined to be too costly. Thus, dry blending is the only proposed disposal process for the uranium oxide materials in the CPP-651 vault. Isotopic dilution of HEU to typically less than 20% by dry blending is the key to solving the dispositioning issue (i.e., proliferation) posed by HEU stored at INEEL. RM-2 mill is a technology developed and successfully tested for producing ultra-fine particles by dry grinding. Grinding action in RM-2 mill produces a two million-fold increase in the number of particles being blended in a centrifugal field. In a previous study, the concept of achieving complete and adequate blending and mixing (i.e., no methods were identified to easily separate and concentrate one titanium compound from the other) in remarkably short processing times was successfully tested with surrogate materials (titanium dioxide and titanium mono-oxide) with different particle sizes, hardness and densities. In the current project, the RM-2 milling technology was thoroughly tested with mixtures of natural uranium oxide (NU) and depleted uranium oxide (DU) stock to prove its performance. The effects of mill operating and design variables on the blending of NU/DU oxides were evaluated. First, NU and DU both made of the same oxide, UO{sub 3}, was used in the testing. Next, NU made up of UO{sub 3} and DU made up of UO{sub 2} was used in the test work. In every test, the blend achieved was characterized by spatial sampling of the ground product and analyzing for {sup 235}U concentration. The test work proved that these uranium oxide materials can be blended successfully. The spatial concentration was found to be uniform. Next, sintered thorium oxide pellets were used as surrogate for light water breeder reactor pellets (LWBR). To simulate LWBR pellet dispositioning, the thorium oxide pellets were first ground to a powder form and then the powder was blended with NU. In these tests also the concentration of {sup 235}U and {sup 232}Th in blended products fell within established limits proving the success of RM-2 milling technology. RM-2 milling technology is applicable to any dry radioactive waste, especially brittle solids that can be ground up and mixed with the non-radioactive stock.

Raj K. Rajamani; Sanjeeva Latchireddi; Vikas Devrani; Harappan Sethi; Roger Henry; Nate Chipman

2003-08-01T23:59:59.000Z

118

Transmutation Analysis of Enriched Uranium and Deep Burn High Temperature Reactors  

SciTech Connect (OSTI)

High temperature reactors (HTRs) have been under consideration for production of electricity, process heat, and for destruction of transuranics for decades. As part of the transmutation analysis efforts within the Fuel Cycle Research and Development (FCR&D) campaign, a need was identified for detailed discharge isotopics from HTRs for use in the VISION code. A conventional HTR using enriched uranium in UCO fuel was modeled having discharge burnup of 120 GWd/MTiHM. Also, a deep burn HTR (DB-HTR) was modeled burning transuranic (TRU)-only TRU-O2 fuel to a discharge burnup of 648 GWd/MTiHM. For each of these cases, unit cell depletion calculations were performed with SCALE/TRITON. Unit cells were used to perform this analysis using SCALE 6.1. Because of the long mean free paths (and migration lengths) of neutrons in HTRs, using a unit cell to represent a whole core can be non-trivial. The sizes of these cells were first set by using Serpent calculations to match a spectral index between unit cell and whole core domains. In the case of the DB-HTR, the unit cell which was arrived at in this way conserved the ratio of fuel to moderator found in a single block of fuel. In the conventional HTR case, a larger moderator-to-fuel ratio than that of a single block was needed to simulate the whole core spectrum. Discharge isotopics (for 500 nuclides) and one-group cross-sections (for 1022 nuclides) were delivered to the transmutation analysis team. This report provides documentation for these calculations. In addition to the discharge isotopics, one-group cross-sections were provided for the full list of 1022 nuclides tracked in the transmutation library.

Michael A. Pope

2012-07-01T23:59:59.000Z

119

Monte Carlo modeling and analyses of YALINA booster subcritical assembly, Part III : low enriched uranium conversion analyses.  

SciTech Connect (OSTI)

This study investigates the performance of the YALINA Booster subcritical assembly, located in Belarus, during operation with high (90%), medium (36%), and low (21%) enriched uranium fuels in the assembly's fast zone. The YALINA Booster is a zero-power, subcritical assembly driven by a conventional neutron generator. It was constructed for the purpose of investigating the static and dynamic neutronics properties of accelerator driven subcritical systems, and to serve as a fast neutron source for investigating the properties of nuclear reactions, in particular transmutation reactions involving minor-actinides. The first part of this study analyzes the assembly's performance with several fuel types. The MCNPX and MONK Monte Carlo codes were used to determine effective and source neutron multiplication factors, effective delayed neutron fraction, prompt neutron lifetime, neutron flux profiles and spectra, and neutron reaction rates produced from the use of three neutron sources: californium, deuterium-deuterium, and deuterium-tritium. In the latter two cases, the external neutron source operates in pulsed mode. The results discussed in the first part of this report show that the use of low enriched fuel in the fast zone of the assembly diminishes neutron multiplication. Therefore, the discussion in the second part of the report focuses on finding alternative fuel loading configurations that enhance neutron multiplication while using low enriched uranium fuel. It was found that arranging the interface absorber between the fast and the thermal zones in a circular rather than a square array is an effective method of operating the YALINA Booster subcritical assembly without downgrading neutron multiplication relative to the original value obtained with the use of the high enriched uranium fuels in the fast zone.

Talamo, A.; Gohar, Y. (Nuclear Engineering Division) [Nuclear Engineering Division

2011-05-12T23:59:59.000Z

120

Laser and gas centrifuge enrichment  

SciTech Connect (OSTI)

Principles of uranium isotope enrichment using various laser and gas centrifuge techniques are briefly discussed. Examples on production of high enriched uranium are given. Concerns regarding the possibility of using low end technologies to produce weapons grade uranium are explained. Based on current assessments commercial enrichment services are able to cover the global needs of enriched uranium in the foreseeable future.

Heinonen, Olli [Senior Fellow, Belfer Center for Science and International Affairs, Harvard Kennedy School, Cambridge, Massachusetts (United States)

2014-05-09T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


121

Uranium Ore Uranium is extracted  

E-Print Network [OSTI]

Milling of Uranium Ore Uranium is extracted from ore with strong acids or bases. The uranium is concentrated in a solid substance called"yellowcake." Chemical Conversion Plants convert the uranium in yellowcake to uranium hexafluoride (UF6 ), a compound that can be made into nuclear fuel. Enrichment

122

Compton DIV: Using a Compton-Based Gamma-Ray Imager for Design Information Verification of Uranium Enrichment Plants  

SciTech Connect (OSTI)

A feasibility study has been performed to determine the potential usefulness of Compton imaging as a tool for design information verification (DIV) of uranium enrichment plants. Compton imaging is a method of gamma-ray imaging capable of imaging with a 360-degree field of view over a broad range of energies. These systems can image a room (with a time span on the order of one hour) and return a picture of the distribution and composition of radioactive material in that room. The effectiveness of Compton imaging depends on the sensitivity and resolution of the instrument as well the strength and energy of the radioactive material to be imaged. This study combined measurements and simulations to examine the specific issue of UF{sub 6} gas flow in pipes, at various enrichment levels, as well as hold-up resulting from the accumulation of enriched material in those pipes. It was found that current generation imagers could image pipes carrying UF{sub 6} in less than one hour at moderate to high enrichment. Pipes with low enriched gas would require more time. It was also found that hold-up was more amenable to this technique and could be imaged in gram quantities in a fraction of an hour. another questions arises regarding the ability to separately image two pipes spaced closely together. This depends on the capabilities of the instrument in question. These results are described in detail. In addition, suggestions are given as to how to develop Compton imaging as a tool for DIV.

Burks, M; Verbeke, J; Dougan, A; Wang, T; Decman, D

2009-07-04T23:59:59.000Z

123

Evaluation of a RF-Based Approach for Tracking UF6 Cylinders at a Uranium Enrichment Plant  

SciTech Connect (OSTI)

Approved industry-standard cylinders are used globally to handle and store uranium hexafluoride (UF{sub 6}) feed, product, tails, and samples at uranium enrichment plants. The International Atomic Energy Agency (IAEA) relies on time-consuming physical inspections to verify operator declarations and detect possible diversion of UF{sub 6}. Development of a reliable, automated, and tamper-resistant system for near real-time tracking and monitoring UF{sub 6} cylinders (as they move within an enrichment facility) would greatly improve the inspector function. This type of system can reduce the risk of false or misreported cylinder tare weights, diversion of nuclear material, concealment of excess production, utilization of undeclared cylinders, and misrepresentation of the cylinders contents. This paper will describe a proof-of-concept approach that was designed to evaluate the feasibility of using radio frequency (RF)-based technologies to track individual UF{sub 6} cylinders throughout a portion of their life cycle, and thus demonstrate the potential for improved domestic accountability of materials, and a more effective and efficient method for application of site-level IAEA safeguards. The evaluation system incorporates RF-based identification devices (RFID) which provide a foundation for establishing a reliable, automated, and near real-time tracking system that can be set up to utilize site-specific, rules-based detection algorithms. This paper will report results from a proof-of-concept demonstration at a real enrichment facility that is specifically designed to evaluate both the feasibility of using RF to track cylinders and the durability of the RF equipment to survive the rigors of operational processing and handling. The paper also discusses methods for securely attaching RF devices and describes how the technology can effectively be layered with other safeguard systems and approaches to build a robust system for detecting cylinder diversion. Additionally, concepts for off-site tracking of cylinders are described.

Pickett, Chris A [ORNL] [ORNL; Younkin, James R [ORNL] [ORNL; Kovacic, Donald N [ORNL] [ORNL; Laughter, Mark D [ORNL] [ORNL; Hines, Jairus B [ORNL] [ORNL; Boyer, Brian [Los Alamos National Laboratory (LANL)] [Los Alamos National Laboratory (LANL); Martinez, B. [Los Alamos National Laboratory (LANL)] [Los Alamos National Laboratory (LANL)

2008-01-01T23:59:59.000Z

124

Design Study for a Low-enriched Uranium Core for the High Flux Isotope Reactor, Annual Report for FY 2007  

SciTech Connect (OSTI)

This report documents progress made during fiscal year 2007 in studies of converting the High Flux Isotope Reactor (HFIR) from highly enriched uranium (HEU) fuel to low enriched uranium fuel (LEU). Conversion from HEU to LEU will require a change in fuel form from uranium oxide to a uranium-molybdenum alloy. A high volume fraction U/Mo-in-Al fuel could attain the same neutron flux performance as with the current, HEU fuel but materials considerations appear to preclude production and irradiation of such a fuel. A diffusion barrier would be required if Al is to be retained as the interstitial medium and the additional volume required for this barrier would degrade performance. Attaining the high volume fraction (55 wt. %) of U/Mo assumed in the computational study while maintaining the current fuel plate acceptance level at the fuel manufacturer is unlikely, i.e. no increase in the percentage of plates rejected for non-compliance with the fuel specification. Substitution of a zirconium alloy for Al would significantly increase the weight of the fuel element, the cost of the fuel element, and introduce an as-yet untried manufacturing process. A monolithic U-10Mo foil is the choice of LEU fuel for HFIR. Preliminary calculations indicate that with a modest increase in reactor power, the flux performance of the reactor can be maintained at the current level. A linearly-graded, radial fuel thickness profile is preferred to the arched profile currently used in HEU fuel because the LEU fuel media is a metal alloy foil rather than a powder. Developments in analysis capability and nuclear data processing techniques are underway with the goal of verifying the preliminary calculations of LEU flux performance. A conceptual study of the operational cost of an LEU fuel fabrication facility yielded the conclusion that the annual fuel cost to the HFIR would increase significantly from the current, HEU fuel cycle. Though manufacturing can be accomplished with existing technology, several engineering proof-of-principle tests would be required. The RERTR program is currently conducting a series of generic fuel qualification tests at the Advanced Test Reactor. A review of these tests and a review of the safety basis for the current, HEU fuel cycle led to the identification of a set of HFIR-specific fuel qualification tests. Much additional study is required to formulate a HFIR-specific fuel qualification plan from this set. However, one such test - creating a graded fuel profile across a flat foil - has been initiated with promising results.

Primm, Trent [ORNL; Ellis, Ronald James [ORNL; Gehin, Jess C [ORNL; Ilas, Germina [ORNL; Miller, James Henry [ORNL; Sease, John D [ORNL

2007-11-01T23:59:59.000Z

125

RERTR program activities related to the development and application of new LEU fuels. [Reduced Enrichment Research and Test Reactor; low-enriched uranium  

SciTech Connect (OSTI)

The statue of the U.S. Reduced Enrichment Research and Test Reactor (RERTR) Program is reviewed. After a brief outline of RERTR Program objectives and goals, program accomplishments are discussed with emphasis on the development, demonstration and application of new LEU fuels. Most program activities have proceeded as planned, and a combination of two silicide fuels (U/sub 3/Si/sub 2/-Al and U/sub 3/Si-Al) holds excellent promise for achieving the long-term program goals. Current plans and schedules project the uranium density of qualified RERTR fuels for plate-type reactors to grow by approximately 1 g U/cm/sup 3/ each year, from the current 1.7 g U/cm/sup 3/ to the 7.0 g U/cm/sup 3/ which will be reached in late 1988. The technical needs of research and test reactors for HEU exports are also forecasted to undergo a gradual but dramatic decline in the coming years.

Travelli, A.

1983-01-01T23:59:59.000Z

126

Parametric Evaluation of Active Neutron Interrogation for the Detection of Shielded Highly-Enriched Uranium in the Field  

SciTech Connect (OSTI)

Parametric studies using numerical simulations are being performed to assess the performance capabilities and limits of active neutron interrogation for detecting shielded highly enriched uranium (HEU). Varying the shield material, HEU mass, HEU depth inside the shield, and interrogating neutron source energy, the simulations account for both neutron and photon emission signatures from the HEU with resolution in both energy and time. The results are processed to represent different irradiation timing schemes and several different classes of radiation detectors, and evaluated using a statistical approach considering signal intensity over background. This paper describes the details of the modeling campaign and some preliminary results, weighing the strengths of alternative measurement approaches for the different irradiation scenarios.

D. L. Chcihester; E. H. Seabury; S. J. Thompson; R. R. C. Clement

2011-10-01T23:59:59.000Z

127

Monte Carlo analysis of the slightly enriched uranium-D/sub 2/O critical experiment LTRIIA (AWBA Development Program)  

SciTech Connect (OSTI)

The Savannah River Laboratory LTRIIA slightly-enriched uranium-D/sub 2/O critical experiment was analyzed with ENDF/B-IV data and the RCP01 Monte Carlo program, which modeled the entire assembly in explicit detail. The integral parameters delta/sup 25/ and delta/sup 28/ showed good agreement with experiment. However, calculated K/sub eff/ was 2 to 3% low, due primarily to an overprediction of U238 capture. This is consistent with results obtained in similar analyses of the H/sub 2/O-moderated TRX critical experiments. In comparisons with the VIM and MCNP2 Monte Carlo programs, good agreement was observed for calculated reeaction rates in the B/sup 2/=0 cell.

Hardy, J. Jr.; Shore, J.M.

1981-11-01T23:59:59.000Z

128

Verification of the MCU precision code and ROSFOND neutron data in application to the calculations of criticality of fast reactors with highly enriched uranium  

SciTech Connect (OSTI)

Calculation of 335 critical assemblies (benchmark experiments) with the core of highly enriched uranium and reflectors of various materials is performed. The statistical analysis of the results shows that, for all 16 materials studied, the absolute value of the most probable deviation of the calculated value of K{sub eff} from the experimental one does not exceed 0.005.

Alekseev, N. I.; Kalugin, M. A.; Kulakov, A. S.; Novosel’tsev, A. P.; Sergeev, G. S.; Shkarovskiy, D. A.; Yudkevich, M. S., E-mail: umark@adis.vver.kiae.ru [National Research Center Kurchatov Institute (Russian Federation)

2014-12-15T23:59:59.000Z

129

Validation of SCALE 4. 0 -- CSAS25 module and the 27-group ENDF/B-IV cross-section library for low-enriched uranium systems  

SciTech Connect (OSTI)

A version of KENO V.a and the 27-group library in SCALE-4.0 were validated for use in evaluating the nuclear criticality safety of low-enriched uranium systems. A total of 59 critical systems were analyzed. A statistical analysis of the results was performed, and subcritical acceptanced criteria are established.

Jordan, W.C.

1993-02-01T23:59:59.000Z

130

Validation of SCALE 4.0 -- CSAS25 module and the 27-group ENDF/B-IV cross-section library for low-enriched uranium systems  

SciTech Connect (OSTI)

A version of KENO V.a and the 27-group library in SCALE-4.0 were validated for use in evaluating the nuclear criticality safety of low-enriched uranium systems. A total of 59 critical systems were analyzed. A statistical analysis of the results was performed, and subcritical acceptanced criteria are established.

Jordan, W.C.

1993-02-01T23:59:59.000Z

131

Assumptions and Criteria for Performing a Feasability Study of the Conversion of the High Flux Isotope Reactor Core to Use Low-Enriched Uranium Fuel  

SciTech Connect (OSTI)

A computational study will be initiated during fiscal year 2006 to examine the feasibility of converting the High Flux Isotope Reactor from highly enriched uranium fuel to low-enriched uranium. The study will be limited to steady-state, nominal operation, reactor physics and thermal-hydraulic analyses of a uranium-molybdenum alloy that would be substituted for the current fuel powder--U{sub 3}O{sub 8} mixed with aluminum. The purposes of this document are to (1) define the scope of studies to be conducted, (2) define the methodologies to be used to conduct the studies, (3) define the assumptions that serve as input to the methodologies, (4) provide an efficient means for communication with the Department of Energy and American research reactor operators, and (5) expedite review and commentary by those parties.

Primm, R.T., III; Ellis, R.J.; Gehin, J.C.; Moses, D.L.; Binder, J.L.; Xoubi, N. (U. of Cincinnati)

2006-02-01T23:59:59.000Z

132

Economic and Non-proliferation Policy Considerations of Uranium Enrichment in Brazil and Argentina  

SciTech Connect (OSTI)

The nuclear development programs of both Argentina and Brazil have, since the 1970s, been premised on the desire for self-sufficiency and assurance of nuclear fuel supply. While military rivalry and mutual distrust led to nuclear weapons related development programs in the 1970s and 1980s, both countries have since terminated these programs. Furthermore, the governments of both countries have pledged their commitment to exclusively non-explosive use of nuclear energy and have signed the Non Proliferation Treaty (NPT). Utilizing rights provided for under the NPT, both Argentina and Brazil have nuclear fuel production facilities, with the notable exception of enrichment plants, that provide much of the current indigenous fuel requirements for their nuclear power plants. However, both countries are actively developing enrichment capability to fill this gap. The purpose of this report is to assess the economic basis and non-proliferation policy considerations for indigenous enrichment capability within the context of their desired self-sufficiency and to evaluate possible United States Government policy options.

Short, Steven M.; Phillips, Jon R.; Weimar, Mark R.; Mahy, Heidi A.

2008-09-01T23:59:59.000Z

133

Assessment of enriched uranium storage safety issues at the Oak Ridge Y-12 Plant  

SciTech Connect (OSTI)

This document is an assessment of the technical safety issues pertaining to the storage of EU at the Oak Ridge Y-12 Plant. The purpose of the assessment is to serve as the basis for defining the technical standards for storage of EU at Y-12. A formal assessment of the Y-12 materials acceptance criteria for EU is currently being conducted by a task force cochaired by B. G. Eddy of DOE Oak Ridge Operations and S. 0. Cox of Y-12 Defense Programs. The mission of this technical assessment for storage is obviously dependent on results of the acceptance assessment. Clearly, the two efforts require coordination to avoid inconsistencies. In addition, both these Assessments must be consistent with the Environmental Assessment for EU storage at Y-12.1 Both the Storage Assessment and the Criteria for Acceptance must take cognizance of the fact that a portion of the EU to be submitted for storage in the future is expected to be derived from foreign sources and to include previously irradiated uranium containing significant levels of transuranics, radioactive daughter products, and unstable uranium isotopes that do not occur in the EU stream of the DOE weapons complex. National security considerations may dictate that these materials be accepted despite the fact that they fail to conform to the Acceptance Criteria. This document will attempt to address the complexities inherent in this situation.

NONE

1996-08-01T23:59:59.000Z

134

Environmental assessment for the purchase of Russian low enriched uranium derived from the dismantlement of nuclear weapons in the countries of the former Soviet Union  

SciTech Connect (OSTI)

The United States is proposing to purchase from the Russian Federation low enriched uranium (LEU) derived from highly enriched uranium (HEU) resulting from the dismantlement of nuclear weapons in the countries of the former Soviet Union. The purchase would be accomplished through a proposed contract requiring the United States to purchase 15,250 metric tons (tonnes) of LEU (or 22,550 tonnes of UF{sub 6}) derived from blending 500 metric tones uranium (MTU) of HEU from nuclear warheads. The LEU would be in the form of uranium hexafluoride (UF{sub 6}) and would be converted from HEU in Russia. The United States Enrichment Corporation (USEC) is the entity proposing to undertake the contract for purchase, sale, and delivery of the LEU from the Russian Federation. The US Department of Energy (DOE) is negotiating the procedure for gaining confidence that the LEU is derived from HEU that is derived from dismantled nuclear weapons (referred to as ``transparency),`` and would administer the transparency measures for the contract. There are six environments that could potentially be affected by the proposed action; marine (ocean); US ports of entry; truck or rail transportation corridors; the Portsmouth GDP; the electric power industry; and the nuclear fuel cycle industry. These environmental impacts are discussed.

Not Available

1994-01-01T23:59:59.000Z

135

Direct fissile assay of enriched uranium using random self-interrogation and neutron coincidence response  

DOE Patents [OSTI]

Apparatus and method for the direct, nondestructive evaluation of the .sup.235 U nuclide content of samples containing UF.sub.6, UF.sub.4, or UO.sub.2 utilizing the passive neutron self-interrogation of the sample resulting from the intrinsic production of neutrons therein. The ratio of the emitted neutron coincidence count rate to the total emitted neutron count rate is determined and yields a measure of the bulk fissile mass. The accuracy of the method is 6.8% (1.sigma.) for cylinders containing UF.sub.6 with enrichments ranging from 6% to 98% with measurement times varying from 3-6 min. The samples contained from below 1 kg to greater than 16 kg. Since the subject invention relies on fast neutron self-interrogation, complete sampling of the UF.sub.6 takes place, reducing difficulties arising from inhomogeneity of the sample which adversely affects other assay procedures.

Menlove, Howard O. (Los Alamos, NM); Stewart, James E. (Los Alamos, NM)

1986-01-01T23:59:59.000Z

136

Direct fissile assay of enriched uranium using random self-interrogation and neutron coincidence response  

DOE Patents [OSTI]

Apparatus and method for the direct, nondestructive evaluation of the /sup 235/U nuclide content of samples containing UF/sub 6/, UF/sub 4/, or UO/sub 2/ utilizing the passive neutron self-interrogation of the sample resulting from the intrinsic production of neutrons therein. The ratio of the emitted neutron coincidence count rate to the total emitted neutron count rate is determined and yields a measure of the bulk fissile mass. The accuracy of the method is 6.8% (1sigma) for cylinders containing UF/sub 6/ with enrichments ranging from 6% to 98% with measurement times varying from 3-6 min. The samples contained from below 1 kg to greater than 16 kg. Since the subject invention relies on fast neutron self-interrogation, complete sampling of the UF/sub 6/ takes place, reducing difficulties arising from inhomogeneity of the sample which adversely affects other assay procedures. 4 figs., 1 tab.

Menlove, H.O.; Stewart, J.E.

1985-02-04T23:59:59.000Z

137

Successful Completion of the Largest Shipment of Russian Research Reactor High-Enriched Uranium Spent Nuclear Fuel from Czech Republic to Russian Federation  

SciTech Connect (OSTI)

On December 8, 2007, the largest shipment of high-enriched uranium spent nuclear fuel was successfully made from a Russian-designed nuclear research reactor in the Czech Republic to the Russian Federation. This accomplishment is the culmination of years of planning, negotiations, and hard work. The United States, Russian Federation, and the International Atomic Energy Agency have been working together on the Russian Research Reactor Fuel Return (RRRFR) Program in support of the Global Threat Reduction Initiative. In February 2003, RRRFR Program representatives met with the Nuclear Research Institute in Rež, Czech Republic, and discussed the return of their high-enriched uranium spent nuclear fuel to the Russian Federation for reprocessing. Nearly 5 years later, the shipment was made. This paper discusses the planning, preparations, coordination, and cooperation required to make this important international shipment.

Michael Tyacke; Dr. Igor Bolshinsky; Jeff Chamberlin

2008-07-01T23:59:59.000Z

138

The Complete Burning of Weapons Grade Plutonium and Highly Enriched Uranium with (Laser Inertial Fusion-Fission Energy) LIFE Engine  

SciTech Connect (OSTI)

The National Ignition Facility (NIF) project, a laser-based Inertial Confinement Fusion (ICF) experiment designed to achieve thermonuclear fusion ignition and burn in the laboratory, is under construction at the Lawrence Livermore National Laboratory (LLNL) and will be completed in April of 2009. Experiments designed to accomplish the NIF's goal will commence in late FY2010 utilizing laser energies of 1 to 1.3 MJ. Fusion yields of the order of 10 to 20 MJ are expected soon thereafter. Laser initiated fusion-fission (LIFE) engines have now been designed to produce nuclear power from natural or depleted uranium without isotopic enrichment, and from spent nuclear fuel from light water reactors without chemical separation into weapons-attractive actinide streams. A point-source of high-energy neutrons produced by laser-generated, thermonuclear fusion within a target is used to achieve ultra-deep burn-up of the fertile or fissile fuel in a sub-critical fission blanket. Fertile fuels including depleted uranium (DU), natural uranium (NatU), spent nuclear fuel (SNF), and thorium (Th) can be used. Fissile fuels such as low-enrichment uranium (LEU), excess weapons plutonium (WG-Pu), and excess highly-enriched uranium (HEU) may be used as well. Based upon preliminary analyses, it is believed that LIFE could help meet worldwide electricity needs in a safe and sustainable manner, while drastically shrinking the nation's and world's stockpile of spent nuclear fuel and excess weapons materials. LIFE takes advantage of the significant advances in laser-based inertial confinement fusion that are taking place at the NIF at LLNL where it is expected that thermonuclear ignition will be achieved in the 2010-2011 timeframe. Starting from as little as 300 to 500 MW of fusion power, a single LIFE engine will be able to generate 2000 to 3000 MWt in steady state for periods of years to decades, depending on the nuclear fuel and engine configuration. Because the fission blanket in a fusion-fission hybrid system is subcritical, a LIFE engine can burn any fertile or fissile nuclear material, including unenriched natural or depleted U and SNF, and can extract a very high percentage of the energy content of its fuel resulting in greatly enhanced energy generation per metric ton of nuclear fuel, as well as nuclear waste forms with vastly reduced concentrations of long-lived actinides. LIFE engines could thus provide the ability to generate vast amounts of electricity while greatly reducing the actinide content of any existing or future nuclear waste and extending the availability of low cost nuclear fuels for several thousand years. LIFE also provides an attractive pathway for burning excess weapons Pu to over 99% FIMA (fission of initial metal atoms) without the need for fabricating or reprocessing mixed oxide fuels (MOX). Because of all of these advantages, LIFE engines offer a pathway toward sustainable and safe nuclear power that significantly mitigates nuclear proliferation concerns and minimizes nuclear waste. An important aspect of a LIFE engine is the fact that there is no need to extract the fission fuel from the fission blanket before it is burned to the desired final level. Except for fuel inspection and maintenance process times, the nuclear fuel is always within the core of the reactor and no weapons-attractive materials are available outside at any point in time. However, an important consideration when discussing proliferation concerns associated with any nuclear fuel cycle is the ease with which reactor fuel can be converted to weapons usable materials, not just when it is extracted as waste, but at any point in the fuel cycle. Although the nuclear fuel remains in the core of the engine until ultra deep actinide burn up is achieved, soon after start up of the engine, once the system breeds up to full power, several tons of fissile material is present in the fission blanket. However, this fissile material is widely dispersed in millions of fuel pebbles, which can be tagged as individual accountable items, and thus made difficult to diver

Farmer, J C; Diaz de la Rubia, T; Moses, E

2008-12-23T23:59:59.000Z

139

EA-1977: Acceptance and Disposition of Used Nuclear Fuel Containing U.S.-Origin Highly Enriched Uranium from the Federal Republic of Germany  

Broader source: Energy.gov [DOE]

This environmental assessment (EA) will evaluate the potential environmental impacts of a DOE proposal to accept used nuclear fuel from the Federal Republic of Germany at DOE’s Savannah River Site (SRS) for processing and disposition. This used nuclear fuel is composed of kernels containing thorium and U.S.-origin highly enriched uranium (HEU) embedded in small graphite spheres that were irradiated in nuclear reactors used for research and development purposes.

140

Feasibility studies to establish at the Kazakhstan Ulba metallurgical plant the manufacturing capability to produce low-enriched uranium certified reference materials  

SciTech Connect (OSTI)

One of the salient features of the transition plan that the United States Department of Energy/National Nuclear Security Administration (DOE/NNSA) is presently implementing in the Former Soviet Union countries is the availability of uranium certified reference materials for calibration of nondestructive assay (NDA) measurement equipment. To address this challenge, DOE/NNSA and U.S. national laboratories have focused their cooperative efforts on establishing a reliable source for manufacturing, certifying, and supplying of such standards. The Ulba Metallurgical Plant (UMP), Kazakhstan, which processes large quantities of low-enriched uranium to produce ceramic fuel pellets for nuclear-powered reactors, is well situated to become a key supplier of low-enriched uranium certified reference materials for the country and Central Asia region. We have recently completed Phase I of a feasibility study to establish at UMP capabilities of manufacturing these standards. In this paper we will discuss details of a proposed methodology for uranium down-blending, material selection and characterization, and a proposed methodology of measurement by destructive (DA) and non-destructive (NDA) analysis to form a database for material certification by the competent State authorities in the Republic of Kazakhstan. In addition, we will discuss the prospect for manufacturing of such standards at UMP.

Kuzminski, Jozef [Los Alamos National Laboratory; Nesuhoff, J [NBL; Cratto, P [NBL; Pfennigwerth, G [Y12 NATIONAL SEC. COMPLEX; Mikhailenko, A [ULBA METALLURGICAL PLANT; Maliutina, I [ULBA METALLURGICAL PLANT; Nations, J [GREGG PROTECTION SERVICES

2009-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


141

H. R. 4934: This title may be cited as the Uranium Revitalization, Tailings Reclamation and Enrichment Act of 1988. Introduced in the House of Representatives, One Hundredth Congress, Second Session, June 28, 1988  

SciTech Connect (OSTI)

H.R. 4934 is a bill to provide for a viable domestic uranium industry, to establish a program to fund reclamation and other remedial actions with respect to mill tailings at active uranium and thorium sites, to establish a wholly-owned Government corporation to manage the Nation's uranium enrichment enterprise, operating as a continuing, commercial enterprise on a profitable and efficient basis, and for other purposes.

Not Available

1988-01-01T23:59:59.000Z

142

SUB-LEU-METAL-THERM-001 SUBCRITICAL MEASUREMENTS OF LOW ENRICHED TUBULAR URANIUM METAL FUEL ELEMENTS BEFORE & AFTER IRRADIATION  

SciTech Connect (OSTI)

With the shutdown of the Hanford PUREX (Plutonium-Uranium Extraction Plant) reprocessing plant in the 1970s, adequate storage capacity for spent Hanford N Reactor fuel elements in the K and N Reactor pools became a concern. To maximize space utilization in the pools, accounting for fuel burnup was considered. Calculations indicated that at typical fuel exposures for N Reactor, the spent-fuel critical mass would be twice the critical mass for green fuel. A decision was reached to test the calculational result with a definitive experiment. If the results proved positive, storage capacity could be increased and N Reactor operation could be prolonged. An experiment to be conducted in the N Reactor spent-fuel storage pool was designed and assembled and the services of the Battelle Northwest Laboratories (BNWL) (now Pacific Northwest National Laboratory [PNNL]) critical mass laboratory were procured for the measurements. The experiments were performed in April 1975 in the Hanford N Reactor fuel storage pool. The fuel elements were MKIA fuel assemblies, comprising two concentric tubes of low-enriched metallic uranium. Two separate sets of measurements were performed: one with ''green'' (fresh) fuel and one with spent fuel. Both the green and spent fuel, were measured in the same geometry. The spent-fuel MKIA assemblies had an average burnup of 2865 MWd (megawatt days)/t. A constraint was imposed restricting the measurements to a subcritical limit of k{sub eff} = 0.97. Subcritical count rate data was obtained with pulsed-neutron and approach-to-critical measurements. Ten (10) configurations with green fuel and nine (9) configurations with spent fuel are described and evaluated. Of these, 3 green fuel and 4 spent fuel loading configurations were considered to serve as benchmark models. However, shortcomings in experimental data failed to meet the high standards for a benchmark problem. Nevertheless, the data provided by these subcritical measurements can supply useful information to analysts evaluating spent fuel subcriticality. The original purpose of the subcritical measurements was to validate computer model predictions that spent N Reactor fuel of a particular, typical exposure (2740 MWd/t) had a critical mass equal to twice that of unexposed fuel of the same type. The motivation for performing this work was driven by the need to increase spent fuel storage limits. These subcritical measurements confirmed the computer model predictions.

SCHWINKENDORF, K.N.

2006-05-12T23:59:59.000Z

143

Uranium industry annual 1996  

SciTech Connect (OSTI)

The Uranium Industry Annual 1996 (UIA 1996) provides current statistical data on the US uranium industry`s activities relating to uranium raw materials and uranium marketing. The UIA 1996 is prepared for use by the Congress, Federal and State agencies, the uranium and nuclear electric utility industries, and the public. Data on uranium raw materials activities for 1987 through 1996 including exploration activities and expenditures, EIA-estimated reserves, mine production of uranium, production of uranium concentrate, and industry employment are presented in Chapter 1. Data on uranium marketing activities for 1994 through 2006, including purchases of uranium and enrichment services, enrichment feed deliveries, uranium fuel assemblies, filled and unfilled market requirements, uranium imports and exports, and uranium inventories are shown in Chapter 2. A feature article, The Role of Thorium in Nuclear Energy, is included. 24 figs., 56 tabs.

NONE

1997-04-01T23:59:59.000Z

144

SUB-LEU-METAL-THERM-001 SUBCRITICAL MEASUREMENTS OF LOW ENRICHED TUBULAR URANIUM METAL FUEL ELEMENTS BEFORE & AFTER IRRADIATION  

SciTech Connect (OSTI)

With the shutdown of the Hanford PUREX (Plutonium-Uranium Extraction Plant) reprocessing plant in the 1970s, adequate storage capacity for spent Hanford N Reactor fuel elements in the K and N Reactor pools became a concern. To maximize space utilization in the pools, accounting for fuel burnup was considered. Fuel that had experienced a neutron environment in a reactor is known as spent, exposed, or irradiated fuel. In contrast fuel that has not yet been placed in a reactor is known as green, unexposed, or unirradiated fuel. Calculations indicated that at typical fuel exposures for N Reactor, the spent-fuel critical mass would be twice the critical mass for green fuel. A decision was reached to test the calculational result with a definitive experiment. If the results proved positive, storage capacity could be increased and N Reactor operation could be prolonged. An experiment to be conducted in the N Reactor spent-fuel storage pool was designed and assembled (References 1 and 2) and the services of the Battelle Northwest Laboratories (BNWL) (now Pacific Northwest National Laboratory [PNNL]) critical mass laboratory were procured for the measurements (Reference 3). The experiments were performed in April 1975 in the Hanford N Reactor fuel storage pool. The fuel elements were MKIA fuel assemblies, comprised of two concentric tubes of low-enriched metallic uranium. Two separate sets of measurements were performed: one with unirradiated fuel and one with irradiated fuel. Both the unirradiated and irradiated fuel, were measured in the same geometry. The spent-fuel MKIA assemblies had an average burnup of 2865 MWd (megawatt days)/t. A constraint was imposed restricting the measurements to a subcritical limit of k{sub eff} = 0.97. Subcritical count rate data was obtained with pulsed-neutron and approach-to-critical measurements. Ten (10) configurations with green fuel and nine (9) configurations with spent fuel are described and evaluated. Of these, three (3) green fuel and four (4) spent fuel loading configurations were considered to serve as benchmark models. However, shortcomings in experimental data, such as the uncertainty in fuel exposure impact on reactivity and the pulse neutron data evaluation methodology, failed to meet the high standards for a benchmark problem. Nevertheless, the data provided by these subcritical measurements supply useful information to analysts evaluating spent fuel subcriticality. The original purpose of the subcritical measurements was to validate computer model predictions that spent N Reactor fuel of a particular, typical exposure (2740 MWd/t) had a critical mass equal to twice that of unexposed fuel of the same type. The motivation for performing this work was driven by the need to increase spent fuel storage limits. These subcritical measurements confirmed the computer model predictions.

TOFFER, H.

2006-07-18T23:59:59.000Z

145

Experiments and Simulations of the Use of Time-Correlated Thermal Neutron Counting to Determine the Multiplication of an Assembly of Highly Enriched Uranium  

SciTech Connect (OSTI)

A series of experiments and numerical simulations using thermal-neutron time-correlated measurements has been performed to determine the neutron multiplication, M, of assemblies of highly enriched uranium available at Idaho National Laboratory. The experiments used up to 14.4 kg of highly-enriched uranium, including bare assemblies and assemblies reflected with high-density polyethylene, carbon steel, and tungsten. A small 252Cf source was used to initiate fission chains within the assembly. Both the experiments and the simulations used 6-channel and 8-channel detector systems, each consisting of 3He proportional counters moderated with polyethylene; data was recorded in list mode for analysis. 'True' multiplication values for each assembly were empirically derived using basic neutron production and loss values determined through simulation. A total of one-hundred and sixteen separate measurements were performed using fifty-seven unique measurement scenarios, the multiplication varied from 1.75 to 10.90. This paper presents the results of these comparisons and discusses differences among the various cases.

David L. Chichester; Mathew T. Kinlaw; Scott M. Watson; Jeffrey M. Kalter; Eric C. Miller; William A. Noonan

2014-11-01T23:59:59.000Z

146

DEPARTMENT OF ENERGY Excess Uranium Management: Effects of DOE...  

Broader source: Energy.gov (indexed) [DOE]

Excess Uranium Management: Effects of DOE Transfers of Excess Uranium on Domestic Uranium Mining, Conversion, and Enrichment Industries; Request for Information AGENCY: Office of...

147

Application of the HGSYSTEM/UF{sub 6} model to simulate atmospheric dispersion of UF{sub 6} releases from uranium enrichment plants  

SciTech Connect (OSTI)

Uranium hexafluoride is a dense, reactive gas used in Gaseous Diffusion Plants (GDPs) to make uranium enriched in the {sup 235}U isotope. Large quantities of UF{sub 6} exist at the GDPs in the form of in-process gas and as a solid in storage cylinders; smaller amounts exist as hot liquid during transfer operations. If liquid UF{sub 6} is released to the environment, it immediately flashes to a solid and a dense gas that reacts rapidly with water vapor in the air to form solid particles of uranyl fluoride and hydrogen fluoride gas. Preliminary analyses were done on various accidental release scenarios to determine which scenarios must be considered in the safety analyses for the GDPS. These scenarios included gas releases due to failure of process equipment and liquid/gas releases resulting from a breach of transfer piping from a cylinder. A major goal of the calculations was to estimate the response time for mitigating actions in order to limit potential off-site consequences of these postulated releases. The HGSYSTEM/UF{sub 6} code was used to assess the consequences of these release scenarios. Inputs were developed from release calculations which included two-phase, choked flow followed by expansion to atmospheric pressure. Adjustments were made to account for variable release rates and multiple release points. Superpositioning of outputs and adjustments for exposure time were required to evaluate consequences based on health effects due to exposures to uranium and HF at a specific location.

Goode, W.D. Jr.; Bloom, S.G.; Keith, K.D. Jr.

1995-03-01T23:59:59.000Z

148

Results from a "Proof-of-Concept" Demonstration of RF-Based Tracking of UF6 Cylinders during a Processing Operation at a Uranium Enrichment Plant  

SciTech Connect (OSTI)

Approved industry-standard cylinders are used globally for processing, storing, and transporting uranium hexafluoride (UF{sub 6}) at uranium enrichment plants. To ensure that cylinder movements at enrichment facilities occur as declared, the International Atomic Energy Agency (IAEA) must conduct time-consuming periodic physical inspections to validate facility records, cylinder identity, and containment. By using a robust system design that includes the capability for real-time unattended monitoring (of cylinder movements), site-specific rules-based event detection algorithms, and the capability to integrate with other types of monitoring technologies, one can build a system that will improve overall inspector effectiveness. This type of monitoring system can provide timely detection of safeguard events that could be used to ensure more timely and appropriate responses by the IAEA. It also could reduce reliance on facility records and have the additional benefit of enhancing domestic safeguards at the installed facilities. This paper will discuss the installation and evaluation of a radio-frequency- (RF-) based cylinder tracking system that was installed at a United States Enrichment Corporation Centrifuge Facility. This system was installed primarily to evaluate the feasibility of using RF technology at a site and the operational durability of the components under harsh processing conditions. The installation included a basic system that is designed to support layering with other safeguard system technologies and that applies fundamental rules-based event processing methodologies. This paper will discuss the fundamental elements of the system design, the results from this site installation, and future efforts needed to make this technology ready for IAEA consideration.

Pickett, Chris A [ORNL] [ORNL; Kovacic, Donald N [ORNL] [ORNL; Whitaker, J Michael [ORNL] [ORNL; Younkin, James R [ORNL] [ORNL; Hines, Jairus B [ORNL] [ORNL; Laughter, Mark D [ORNL] [ORNL; Morgan, Jim [Innovative Solutions] [Innovative Solutions; Carrick, Bernie [USEC] [USEC; Boyer, Brian [Los Alamos National Laboratory (LANL)] [Los Alamos National Laboratory (LANL); Whittle, K. [USEC] [USEC

2008-01-01T23:59:59.000Z

149

WISE Uranium Project - Fact Sheet  

E-Print Network [OSTI]

t in the depleted uranium. For this purpose, we first need to calculate the mass balance of the enrichment process. We then calculate the inhalation doses from the depleted uranium and compare the dose contributions from the nuclides of interest. Mass balance for uranium enrichment at Paducah [DOE_1984, p.35] Feed Product Tails Other Mass [st] 758002 124718 621894 11390 Mass fraction 100.00% 16.45% 82.04% 1.50% Concentration of plutonium in tails (depleted uranium) from enrichment of reprocessed uranium, assuming that all plutonium were transfered to the tails: Concentration of neptunium in tails from enrichment of reprocessed uranium uranium, assuming that all neptunium were transfered to the tails: - 2 - Schematic of historic uranium enrichment process at Paducah [DOE_1999b] - -7 For comparison, we first calculate the inhalation dose from depleted uranium produced from natural uranium. We assume that the short-lived decay products have reached secular equilibrium with th

Hazards From Depleted

150

Progress in developing processes for converting {sup 99}Mo production from high- to low-enriched uranium--1998.  

SciTech Connect (OSTI)

During 1998, the emphasis of our activities was focused mainly on target fabrication. Successful conversion requires a reliable irradiation target; the target being developed uses thin foils of uranium metal, which can be removed from the target hardware for dissolution and processing. This paper describes successes in (1) improving our method for heat-treating the uranium foil to produce a random-small grain structure, (2) improving electrodeposition of zinc and nickel fission-fragment barriers onto the foil, and (3) showing that these fission fragment barriers should be stable during transport of the targets following irradiation. A method was also developed for quantitatively electrodepositing uranium and plutonium contaminants in the {sup 99}Mo. Progress was also made in broadening international cooperation in our development activities.

Conner, C.

1998-10-28T23:59:59.000Z

151

Fernald vacuum transfer system for uranium materials repackaging  

SciTech Connect (OSTI)

The Fernald Environmental Management Project (FEMP) is the site of a former Department of Energy (DOE) uranium processing plant. When production was halted, many materials were left in an intermediate state. Some of this product material included enriched uranium compounds that had to be repackaged for shipment of off-site storage. This paper provides an overview, technical description, and status of a new application of existing technology, a vacuum transfer system, to repackage the uranium bearing compounds for shipment. The vacuum transfer system provides a method of transferring compounds from their current storage configuration into packages that meet the Department of Transportation (DOT) shipping requirements for fissile materials. This is a necessary activity, supporting removal of nuclear materials prior to site decontamination and decommissioning, key to the Fernald site's closure process.

Kaushiva, Shirley; Weekley, Clint; Molecke, Martin; Polansky, Gary

2002-02-24T23:59:59.000Z

152

Advanced technologies for decontamination and conversion of scrap metals  

SciTech Connect (OSTI)

Recycle of radioactive scrap metals (RSM) from decommissioning of DOE uranium enrichment and nuclear weapons manufacturing facilities is mandatory to recapture the value of these metals and avoid the high cost of disposal by burial. The scrap metals conversion project detailed below focuses on the contaminated nickel associated with the gaseous diffusion plants. Stainless steel can be produced in MSC`s vacuum induction melting process (VIM) to the S30400 specification using nickel as an alloy constituent. Further the case alloy can be rolled in MSC`s rolling mill to the mechanical property specification for S30400 demonstrating the capability to manufacture the contaminated nickel into valuable end products at a facility licensed to handle radioactive materials. Bulk removal of Technetium from scrap nickel is theoretically possible in a reasonable length of time with the high calcium fluoride flux, however the need for the high temperature creates a practical problem due to flux volatility. Bulk decontamination is possible and perhaps more desirable if nickel is alloyed with copper to lower the melting point of the alloy allowing the use of the high calcium fluoride flux. Slag decontamination processes have been suggested which have been proven technically viable at the Colorado School of Mines.

Muth, T.R. [Manufacturing Sciences Corp., Oak Ridge, TN (United States); Moore, J.; Olson, D.; Mishra, B. [Colorado School of Mines, Golden, CO (United States)

1994-12-31T23:59:59.000Z

153

In-Situ Measurements of Low Enrichment Uranium Holdup Process Gas Piping at K-25 - Paper for Waste Management Symposia 2010 East Tennessee Technology Park Oak Ridge, Tennessee  

SciTech Connect (OSTI)

This document is the final version of a paper submitted to the Waste Management Symposia, Phoenix, 2010, abstract BJC/OR-3280. The primary document from which this paper was condensed is In-Situ Measurement of Low Enrichment Uranium Holdup in Process Gas Piping at K-25 Using NaI/HMS4 Gamma Detection Systems, BJC/OR-3355. This work explores the sufficiency and limitations of the Holdup Measurement System 4 (HJVIS4) software algorithms applied to measurements of low enriched uranium holdup in gaseous diffusion process gas piping. HMS4 has been used extensively during the decommissioning and demolition project of the K-25 building for U-235 holdup quantification. The HMS4 software is an integral part of one of the primary nondestructive assay (NDA) systems which was successfully tested and qualified for holdup deposit quantification in the process gas piping of the K-25 building. The initial qualification focused on the measurement of highly enriched UO{sub 2}F{sub 2} deposits. The purpose of this work was to determine if that qualification could be extended to include the quantification of holdup in UO{sub 2}F{sub 2} deposits of lower enrichment. Sample field data are presented to provide evidence in support of the theoretical foundation. The HMS4 algorithms were investigated in detail and found to sufficiently compensate for UO{sub 2}F{sub 2} source self-attenuation effects, over the range of expected enrichment (4-40%), in the North and East Wings of the K-25 building. The limitations of the HMS4 algorithms were explored for a described set of conditions with respect to area source measurements of low enriched UO{sub 2}F{sub 2} deposits when used in conjunction with a 1 inch by 1/2 inch sodium iodide (NaI) scintillation detector. The theoretical limitations of HMS4, based on the expected conditions in the process gas system of the K-25 building, are related back to the required data quality objectives (DQO) for the NBA measurement system established for the K-25 demolition project. The combined review of the HMS software algorithms and supporting field measurements lead to the conclusion that the majority of process gas pipe measurements are adequately corrected for source self-attenuation using HMS4. While there will be instances where the UO{sub 2}F{sub 2} holdup mass presents an infinitely thick deposit to the NaI-HMS4 system these situations are expected to be infrequent. This work confirms that the HMS4 system can quantify UO{sub 2}F{sub 2} holdup, in its current configuration (deposition, enrichment, and geometry), below the DQO levels for the K-25 building decommissioning and demolition project. For an area measurement of process gas pipe in the K-25 building, if an infinitely thick UO{sub 2}F{sub 2} deposit is identified in the range of enrichment of {approx}4-40%, the holdup quantity exceeds the corresponding DQO established for the K-25 building demolition project.

Rasmussen B.

2010-01-01T23:59:59.000Z

154

Gamma/neutron time-correlation for special nuclear material characterization %3CU%2B2013%3E active stimulation of highly enriched uranium.  

SciTech Connect (OSTI)

A series of simulations and experiments were undertaken to explore and evaluate the potential for a novel new technique for fissile material detection and characterization, the timecorrelated pulse-height (TCPH) method, to be used concurrent with active stimulation of potential nuclear materials. In previous work TCPH has been established as a highly sensitive method for the detection and characterization of configurations of fissile material containing Plutonium in passive measurements. By actively stimulating fission with the introduction of an external radiation source, we have shown that TCPH is also an effective method of detecting and characterizing configurations of fissile material containing Highly Enriched Uranium (HEU). The TCPH method is shown to be robust in the presence of the proper choice of external radiation source. An evaluation of potential interrogation sources is presented.

Marleau, Peter; Nowack, Aaron B.; Clarke, Shaun D. [University of Michigan; Monterial, Mateusz [University of Michigan; Paff, Marc [University of Michigan; Pozzi, Sara A. [University of Michigan

2013-09-01T23:59:59.000Z

155

A study of a zone approach to IAEA (International Atomic Energy Agency) safeguards: The low-enriched-uranium zone of a light-water-reactor fuel cycle  

SciTech Connect (OSTI)

At present the IAEA designs its safeguards approach with regard to each type of nuclear facility so that the safeguards activities and effort are essentially the same for a given type and size of nuclear facility wherever it may be located. Conclusions regarding a state are derived by combining the conclusions regarding the effectiveness of safeguards for the individual facilities within a state. In this study it was convenient to define three zones in a state with a closed light-water-reactor nuclear fuel cycle. Each zone contains those facilities or parts thereof which use or process nuclear materials of the same safeguards significance: low-enriched uranium, radioactive spent fuel, or recovered plutonium. The possibility that each zone might be treated as an extended material balance area for safeguards purposes is under investigation. The approach includes defining the relevant features of the facilities in the three zones and listing the safeguards activities which are now practiced. This study has focussed on the fresh-fuel zone, the several facilities of which use or process low-enriched uranium. At one extreme, flows and inventories would be verified at each material balance area. At the other extreme, the flows into and out of the zone and the inventory of the whole zone would be verified. There are a number of possible safeguards approaches which fall between the two extremes. The intention is to develop a rational approach which will make it possible to compare the technical effectiveness and the inspection effort for the facility-oriented approach, for the approach involving the zone as a material balance area, and for some reasonable intermediate safeguards approaches.

Fishbone, L.G.; Higinbotham, W.A.

1986-06-01T23:59:59.000Z

156

Financial Assurance for In Situ Uranium Facilities (Texas)  

Broader source: Energy.gov [DOE]

Owners or operators are required to provide financial assurance for in situ uranium sites. This money is required for: decommissioning, decontamination, demolition, and waste disposal for buildings...

157

Y-12 Plant Decontamination and Decommissioning Technology Logic Diagram for Building 9201-4. Volume 1: Technology evaluation  

SciTech Connect (OSTI)

During World War 11, the Oak Ridge Y-12 Plant was built as part of the Manhattan Project to supply enriched uranium for weapons production. In 1945, Building 9201-4 (Alpha-4) was originally used to house a uranium isotope separation process based on electromagnetic separation technology. With the startup of the Oak Ridge K-25 Site gaseous diffusion plant In 1947, Alpha-4 was placed on standby. In 1953, the uranium enrichment process was removed, and installation of equipment for the Colex process began. The Colex process--which uses a mercury solvent and lithium hydroxide as the lithium feed material-was shut down in 1962 and drained of process materials. Residual Quantities of mercury and lithium hydroxide have remained in the process equipment. Alpha-4 contains more than one-half million ft{sup 2} of floor area; 15,000 tons of process and electrical equipment; and 23,000 tons of insulation, mortar, brick, flooring, handrails, ducts, utilities, burnables, and sludge. Because much of this equipment and construction material is contaminated with elemental mercury, cleanup is necessary. The goal of the Y-12 Plant Decontamination and Decommissioning Technology Logic Diagram for Building 9201-4 is to provide a planning document that relates decontamination and decommissioning and waste management problems at the Alpha-4 building to the technologies that can be used to remediate these problems. The Y-12 Plant Decontamination and Decommissioning Technology Logic Diagram for Building 9201-4 builds on the methodology transferred by the U.S. Air Force to the Environmental Management organization with DOE and draws from previous technology logic diagram-efforts: logic diagrams for Hanford, the K-25 Site, and ORNL.

NONE

1994-09-01T23:59:59.000Z

158

Decontamination n Sterilization  

E-Print Network [OSTI]

.10 Decontamination Methods #12;n Types n Moist ­ steam n Dry n Incineration *The most effective method Incineration n Method of choice for animal carcasses n Requires certified incinerator 2.10 Decontamination Heat

Collins, Gary S.

159

Uranium Industry Annual, 1992  

SciTech Connect (OSTI)

The Uranium Industry Annual provides current statistical data on the US uranium industry for the Congress, Federal and State agencies, the uranium and electric utility industries, and the public. The feature article, ``Decommissioning of US Conventional Uranium Production Centers,`` is included. Data on uranium raw materials activities including exploration activities and expenditures, resources and reserves, mine production of uranium, production of uranium concentrate, and industry employment are presented in Chapter 1. Data on uranium marketing activities including domestic uranium purchases, commitments by utilities, procurement arrangements, uranium imports under purchase contracts and exports, deliveries to enrichment suppliers, inventories, secondary market activities, utility market requirements, and uranium for sale by domestic suppliers are presented in Chapter 2.

Not Available

1993-10-28T23:59:59.000Z

160

Electroosmotic decontamination of concrete  

SciTech Connect (OSTI)

A method is described for the electroosmotic decontamination of concrete surfaces, in which an electrical field is used to induce migration of ionic contaminants from porous concrete into an electrolyte solution that may be disposed of as a low-level liquid radioactive waste (LLRW); alternately, the contaminants from the solution can be sorbed onto anion exchange media in order to prevent contaminant buildup in the solution and to minimize the amount of LLRW generated. We have confirmed the removal of uranium (and infer the removal of {sup 99}Tc) from previously contaminated concrete surfaces. In a typical experimental configuration, a stainless steel mesh is placed in an electrolyte solution contained within a diked cell to serve as the negative electrode (cathode) and contaminant collection medium, respectively, and an existing metal penetration (e.g., piping, conduit, or rebar reinforcement within the concrete surface) serves as the positive electrode (anode) to complete the cell. Typically we have achieved 70 to >90% reductions in surface activity by applying <400 V and <1 A for 1--3 h (energy consumption of 0.4--12 kWh/ft{sup 2}).

Bostick, W.D.; Bush, S.A.; Marsh, G.C.; Henson, H.M. [Oak Ridge K-25 Site, TN (United States); Box, W.D.; Morgan, I.L. [Oak Ridge National Lab., TN (United States)

1993-03-01T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


161

Reactive decontamination formulation  

DOE Patents [OSTI]

The present invention provides a universal decontamination formulation and method for detoxifying chemical warfare agents (CWA's) and biological warfare agents (BWA's) without producing any toxic by-products, as well as, decontaminating surfaces that have come into contact with these agents. The formulation includes a sorbent material or gel, a peroxide source, a peroxide activator, and a compound containing a mixture of KHSO.sub.5, KHSO.sub.4 and K.sub.2 SO.sub.4. The formulation is self-decontaminating and once dried can easily be wiped from the surface being decontaminated. A method for decontaminating a surface exposed to chemical or biological agents is also disclosed.

Giletto, Anthony (College Station, TX); White, William (College Station, TX); Cisar, Alan J. (Cypress, TX); Hitchens, G. Duncan (Bryan, TX); Fyffe, James (Bryan, TX)

2003-05-27T23:59:59.000Z

162

Preconceptual design of the gas-phase decontamination demonstration cart  

SciTech Connect (OSTI)

Removal of uranium deposits from the interior surfaces of gaseous diffusion equipment will be a major portion of the overall multibillion dollar effort to decontaminate and decommission the gaseous diffusion plants. Long-term low-temperature (LTLT) gas-phase decontamination is being developed at the K-25 Site as an in situ decontamination process that is expected to significantly lower the decontamination costs, reduce worker exposure to radioactive materials, and reduce safeguard concerns. This report documents the preconceptual design of the process equipment that is necessary to conduct a full-scale demonstration of the LTLT method in accordance with the process steps listed above. The process equipment and method proposed in this report are not intended to represent a full-scale production campaign design and operation, since the gas evacuation, gas charging, and off-gas handling systems that would be cost effective in a production campaign are not cost effective for a first-time demonstration. However, the design presented here is expected to be applicable to special decontamination projects beyond the demonstration, which could include the Deposit Recovery Program. The equipment will therefore be sized to a 200 ft size 1 converter (plus a substantial conservative design margin), which is the largest item of interest for gas phase decontamination in the Deposit Recovery Program. The decontamination equipment will allow recovery of the UF{sub 6}, which is generated from the reaction of ClF{sub 3} with the uranium deposits, by use of NaF traps.

Munday, E.B.

1993-12-01T23:59:59.000Z

163

Safeguards Guidance Document for Designers of Commercial Nuclear Facilities: International Nuclear Safeguards Requirements and Practices For Uranium Enrichment Plants  

SciTech Connect (OSTI)

This report is the second in a series of guidelines on international safeguards requirements and practices, prepared expressly for the designers of nuclear facilities. The first document in this series is the description of generic international nuclear safeguards requirements pertaining to all types of facilities. These requirements should be understood and considered at the earliest stages of facility design as part of a new process called “Safeguards-by-Design.” This will help eliminate the costly retrofit of facilities that has occurred in the past to accommodate nuclear safeguards verification activities. The following summarizes the requirements for international nuclear safeguards implementation at enrichment plants, prepared under the Safeguards by Design project, and funded by the U.S. Department of Energy (DOE) National Nuclear Security Administration (NNSA), Office of NA-243. The purpose of this is to provide designers of nuclear facilities around the world with a simplified set of design requirements and the most common practices for meeting them. The foundation for these requirements is the international safeguards agreement between the country and the International Atomic Energy Agency (IAEA), pursuant to the Treaty on the Non-proliferation of Nuclear Weapons (NPT). Relevant safeguards requirements are also cited from the Safeguards Criteria for inspecting enrichment plants, found in the IAEA Safeguards Manual, Part SMC-8. IAEA definitions and terms are based on the IAEA Safeguards Glossary, published in 2002. The most current specification for safeguards measurement accuracy is found in the IAEA document STR-327, “International Target Values 2000 for Measurement Uncertainties in Safeguarding Nuclear Materials,” published in 2001. For this guide to be easier for the designer to use, the requirements have been restated in plainer language per expert interpretation using the source documents noted. The safeguards agreement is fundamentally a legal document. As such, it is written in a legalese that is understood by specialists in international law and treaties, but not by most outside of this field, including designers of nuclear facilities. For this reason, many of the requirements have been simplified and restated. However, in all cases, the relevant source document and passage is noted so that readers may trace the requirement to the source. This is a helpful living guide, since some of these requirements are subject to revision over time. More importantly, the practices by which the requirements are met are continuously modernized by the IAEA and nuclear facility operators to improve not only the effectiveness of international nuclear safeguards, but also the efficiency. As these improvements are made, the following guidelines should be updated and revised accordingly.

Robert Bean; Casey Durst

2009-10-01T23:59:59.000Z

164

Uranium industry annual 1994  

SciTech Connect (OSTI)

The Uranium Industry Annual 1994 (UIA 1994) provides current statistical data on the US uranium industry`s activities relating to uranium raw materials and uranium marketing during that survey year. The UIA 1994 is prepared for use by the Congress, Federal and State agencies, the uranium and nuclear electric utility industries, and the public. It contains data for the 10-year period 1985 through 1994 as collected on the Form EIA-858, ``Uranium Industry Annual Survey.`` Data collected on the ``Uranium Industry Annual Survey`` (UIAS) provide a comprehensive statistical characterization of the industry`s activities for the survey year and also include some information about industry`s plans and commitments for the near-term future. Where aggregate data are presented in the UIA 1994, care has been taken to protect the confidentiality of company-specific information while still conveying accurate and complete statistical data. A feature article, ``Comparison of Uranium Mill Tailings Reclamation in the United States and Canada,`` is included in the UIA 1994. Data on uranium raw materials activities including exploration activities and expenditures, EIA-estimated resources and reserves, mine production of uranium, production of uranium concentrate, and industry employment are presented in Chapter 1. Data on uranium marketing activities, including purchases of uranium and enrichment services, and uranium inventories, enrichment feed deliveries (actual and projected), and unfilled market requirements are shown in Chapter 2.

NONE

1995-07-05T23:59:59.000Z

165

Gross decontamination experiment report  

SciTech Connect (OSTI)

A Gross Decontamination Experiment was conducted on various levels and surfaces of the TMI - Unit 2 reactor building in March 1982. The polar crane, D-rings, missile shields, refueling canals, refueling bridges, equipment, and elevations 305' and 347'-6'' were flushed with low pressure water. Additionally, floor surfaces on elevation 305' and floor surfaces and major pieces of equipment on elevation 347'-6'' were sprayed with high pressure water. Selective surfaces were decontaminated with a mechanical scrubber and chemicals. Strippable coating was tested and evaluated on equipment and floor surfaces. The effectiveness, efficiency, and safety of several decontamination techniques were established for the large, complex decontamination effort. Various decontamination equipment was evaluated and its effectiveness was documented. Decontamination training and procedures were documented and evaluated, as were the support system and organization for the experiment.

Mason, R.; Kinney, K.; Dettorre, J.; Gilbert, V.

1983-07-01T23:59:59.000Z

166

Decontamination and reuse of ORGDP aluminum scrap  

SciTech Connect (OSTI)

The Gaseous Diffusion Plants, or GDPs, have significant amounts of a number of metals, including nickel, aluminum, copper, and steel. Aluminum was used extensively throughout the GDPs because of its excellent strength to weight ratios and good resistance to corrosion by UF{sub 6}. This report is concerned with the recycle of aluminum stator and rotor blades from axial compressors. Most of the stator and rotor blades were made from 214-X aluminum casting alloy. Used compressor blades were contaminated with uranium both as a result of surface contamination and as an accumulation held in surface-connected voids inside of the blades. A variety of GDP studies were performed to evaluate the amounts of uranium retained in the blades; the volume, area, and location of voids in the blades; and connections between surface defects and voids. Based on experimental data on deposition, uranium content of the blades is 0.3%, or roughly 200 times the value expected from blade surface area. However, this value does correlate with estimated internal surface area and with lengthy deposition times. Based on a literature search, it appears that gaseous decontamination or melt refining using fluxes specific for uranium removal have the potential for removing internal contamination from aluminum blades. A melt refining process was used to recycle blades during the 1950s and 1960s. The process removed roughly one-third of the uranium from the blades. Blade cast from recycled aluminum appeared to perform as well as blades from virgin material. New melt refining and gaseous decontamination processes have been shown to provide substantially better decontamination of pure aluminum. If these techniques can be successfully adapted to treat aluminum 214-X alloy, internal and, possibly, external reuse of aluminum alloys may be possible.

Compere, A.L.; Griffith, W.L.; Hayden, H.W.; Wilson, D.F.

1996-12-01T23:59:59.000Z

167

February 2010 Office of Chief Financial Officer DOE/CF-0046  

E-Print Network [OSTI]

.......................................................................................40 Uranium Enrichment Decontamination and Decommissioning Fund ........................................................................................44 Nuclear Energy................................................................55 National Nuclear Security Administration

168

Reactor Physics Methods and Preconceptual Core Design Analyses for Conversion of the Advanced Test Reactor to Low-Enriched Uranium Fuel Annual Report for Fiscal Year 2012  

SciTech Connect (OSTI)

Under the current long-term DOE policy and planning scenario, both the ATR and the ATRC will be reconfigured at an appropriate time within the next several years to operate with low-enriched uranium (LEU) fuel. This will be accomplished under the auspices of the Reduced Enrichment Research and Test Reactor (RERTR) Program, administered by the DOE National Nuclear Security Administration (NNSA). At a minimum, the internal design and composition of the fuel element plates and support structure will change, to accommodate the need for low enrichment in a manner that maintains total core excess reactivity at a suitable level for anticipated operational needs throughout each cycle while respecting all control and shutdown margin requirements and power distribution limits. The complete engineering design and optimization of LEU cores for the ATR and the ATRC will require significant multi-year efforts in the areas of fuel design, development and testing, as well as a complete re-analysis of the relevant reactor physics parameters for a core composed of LEU fuel, with possible control system modifications. Ultimately, revalidation of the computational physics parameters per applicable national and international standards against data from experimental measurements for prototypes of the new ATR and ATRC core designs will also be required for Safety Analysis Report (SAR) changes to support routine operations with LEU. This report is focused on reactor physics analyses conducted during Fiscal Year (FY) 2012 to support the initial development of several potential preconceptual fuel element designs that are suitable candidates for further study and refinement during FY-2013 and beyond. In a separate, but related, effort in the general area of computational support for ATR operations, the Idaho National Laboratory (INL) is conducting a focused multiyear effort to introduce modern high-fidelity computational reactor physics software and associated validation protocols to replace several obsolete components of the current analytical tool set used for ATR neutronics support. This aggressive computational and experimental campaign will have a broad strategic impact on the operation of the ATR, both in terms of improved computational efficiency and accuracy for support of ongoing DOE programs as well as in terms of national and international recognition of the ATR National Scientific User Facility (NSUF). It will also greatly facilitate the LEU conversion effort, since the upgraded computational capabilities are now at a stage where they can be, and in fact have been, used for the required physics analysis from the beginning. In this context, extensive scoping neutronics analyses were completed for six preconceptual candidate LEU fuel element designs for the ATR (and for its companion critical facility, ATRC). Of these, four exhibited neutronics performance in what is believed to be an acceptable range. However, there are currently some concerns with regard to fabricability and mechanical performance that have emerged for one of the four latter concepts. Thus three concepts have been selected for more comprehensive conceptual design analysis during the upcoming fiscal year.

David W. Nigg; Sean R. Morrell

2012-09-01T23:59:59.000Z

169

Long lasting decontamination foam  

DOE Patents [OSTI]

Compositions and methods for decontaminating surfaces are disclosed. More specifically, compositions and methods for decontamination using a composition capable of generating a long lasting foam are disclosed. Compositions may include a surfactant and gelatin and have a pH of less than about 6. Such compositions may further include affinity-shifting chemicals. Methods may include decontaminating a contaminated surface with a composition or a foam that may include a surfactant and gelatin and have a pH of less than about 6.

Demmer, Ricky L. (Idaho Falls, ID); Peterman, Dean R. (Idaho Falls, ID); Tripp, Julia L. (Pocatello, ID); Cooper, David C. (Idaho Falls, ID); Wright, Karen E. (Idaho Falls, ID)

2010-12-07T23:59:59.000Z

170

Statistical sampling method for releasing decontaminated vehicles  

SciTech Connect (OSTI)

Earth moving vehicles (e.g., dump trucks, belly dumps) commonly haul radiologically contaminated materials from a site being remediated to a disposal site. Traditionally, each vehicle must be surveyed before being released. The logistical difficulties of implementing the traditional approach on a large scale demand that an alternative be devised. A statistical method (MIL-STD-105E, {open_quotes}Sampling Procedures and Tables for Inspection by Attributes{close_quotes}) for assessing product quality from a continuous process was adapted to the vehicle decontamination process. This method produced a sampling scheme that automatically compensates and accommodates fluctuating batch sizes and changing conditions without the need to modify or rectify the sampling scheme in the field. Vehicles are randomly selected (sampled) upon completion of the decontamination process to be surveyed for residual radioactive surface contamination. The frequency of sampling is based on the expected number of vehicles passing through the decontamination process in a given period and the confidence level desired. This process has been successfully used for 1 year at the former uranium mill site in Monticello, Utah (a CERCLA regulated clean-up site). The method forces improvement in the quality of the decontamination process and results in a lower likelihood that vehicles exceeding the surface contamination standards are offered for survey. Implementation of this statistical sampling method on Monticello Projects has resulted in more efficient processing of vehicles through decontamination and radiological release, saved hundreds of hours of processing time, provided a high level of confidence that release limits are met, and improved the radiological cleanliness of vehicles leaving the controlled site.

Lively, J.W.; Ware, J.A. [Rust Geotech, Grand Junction, CO (United States)

1996-06-01T23:59:59.000Z

171

EIS-0360: Depleted Uranium Oxide Conversion Product at the Portsmouth, Ohio Site  

Broader source: Energy.gov [DOE]

This site-specific EIS analyzes the construction, operation, maintenance, and decontamination and decommissioning of the proposed depleted uranium hexafluoride (DUF6) conversion facility at three alternative locations within the Paducah site; transportation of all cylinders (DUF6, enriched, and empty) currently stored at the East Tennessee Technology Park (ETTP) near Oak Ridge, Tennessee, to Portsmouth; construction of a new cylinder storage yard at Portsmouth (if required) for ETTP cylinders; transportation of depleted uranium conversion products and waste materials to a disposal facility; transportation and sale of the hydrogen fluoride (HF) produced as a conversion coproduct; and neutralization of HF to calcium fluoride and its sale or disposal in the event that the HF product is not sold.

172

Removal of uranium from uranium-contaminated soils -- Phase 1: Bench-scale testing. Uranium in Soils Integrated Demonstration  

SciTech Connect (OSTI)

To address the management of uranium-contaminated soils at Fernald and other DOE sites, the DOE Office of Technology Development formed the Uranium in Soils Integrated Demonstration (USID) program. The USID has five major tasks. These include the development and demonstration of technologies that are able to (1) characterize the uranium in soil, (2) decontaminate or remove uranium from the soil, (3) treat the soil and dispose of any waste, (4) establish performance assessments, and (5) meet necessary state and federal regulations. This report deals with soil decontamination or removal of uranium from contaminated soils. The report was compiled by the USID task group that addresses soil decontamination; includes data from projects under the management of four DOE facilities [Argonne National Laboratory (ANL), Los Alamos National Laboratory (LANL), Oak Ridge National Laboratory (ORNL), and the Savannah River Plant (SRP)]; and consists of four separate reports written by staff at these facilities. The fundamental goal of the soil decontamination task group has been the selective extraction/leaching or removal of uranium from soil faster, cheaper, and safer than current conventional technologies. The objective is to selectively remove uranium from soil without seriously degrading the soil`s physicochemical characteristics or generating waste forms that are difficult to manage and/or dispose of. Emphasis in research was placed more strongly on chemical extraction techniques than physical extraction techniques.

Francis, C. W.

1993-09-01T23:59:59.000Z

173

Oxidative Tritium Decontamination System  

DOE Patents [OSTI]

The Oxidative Tritium Decontamination System, OTDS, provides a method and apparatus for reduction of tritium surface contamination on various items. The OTDS employs ozone gas as oxidizing agent to convert elemental tritium to tritium oxide. Tritium oxide vapor and excess ozone gas is purged from the OTDS, for discharge to atmosphere or transport to further process. An effluent stream is subjected to a catalytic process for the decomposition of excess ozone to diatomic oxygen. One of two configurations of the OTDS is employed: dynamic apparatus equipped with agitation mechanism and large volumetric capacity for decontamination of light items, or static apparatus equipped with pressurization and evacuation capability for decontamination of heavier, delicate, and/or valuable items.

Gentile, Charles A. (Plainsboro, NJ), Guttadora, Gregory L. (Highland Park, NJ), Parker, John J. (Medford, NJ)

2006-02-07T23:59:59.000Z

174

Decontamination of process equipment using recyclable chelating solvent  

SciTech Connect (OSTI)

The Department of Energy (DOE) is now faced with the task of meeting decontamination and decommissioning obligations at numerous facilities by the year 2019. Due to the tremendous volume of material involved, innovative decontamination technologies are being sought that can reduce the volumes of contaminated waste materials and secondary wastes requiring disposal. With sufficient decontamination, some of the material from DOE facilities could be released as scrap into the commercial sector for recycle, thereby reducing the volume of radioactive waste requiring disposal. Although recycling may initially prove to be more costly than current disposal practices, rapidly increasing disposal costs are expected to make recycling more and more cost effective. Additionally, recycling is now perceived as the ethical choice in a world where the consequences of replacing resources and throwing away reusable materials are impacting the well-being of the environment. Current approaches to the decontamination of metals most often involve one of four basic process types: (1) chemical, (2) manual and mechanical, (3) electrochemical, and (4) ultrasonic. {open_quotes}Hard{close_quotes} chemical decontamination solutions, capable of achieving decontamination factors (Df`s) of 50 to 100, generally involve reagent concentrations in excess of 5%, tend to physically degrade the surface treated, and generate relatively large volumes of secondary waste. {open_quotes}Soft{close_quotes} chemical decontamination solutions, capable of achieving Df`s of 5 to 10, normally consist of reagents at concentrations of 0.1 to 1%, generally leave treated surfaces in a usable condition, and generate relatively low secondary waste volumes. Under contract to the Department of Energy, the Babcock & Wilcox Company is developing a chemical decontamination process using chelating agents to remove uranium compounds and other actinide species from process equipment.

Jevec, J.; Lenore, C.; Ulbricht, S.

1995-12-01T23:59:59.000Z

175

Decontaminating metal surfaces  

DOE Patents [OSTI]

Radioactively contaminated surfaces can be electrolytically decontaminated with greatly increased efficiencies by using electrolytes containing higher than heretofore conventional amounts of nitrate, e.g., >600 g/1 of NaNO/sub 3/, or by using nitrate-containing electrolytes which are acidic, e.g., of a pH < 6.

Childs, E.L.

1984-01-23T23:59:59.000Z

176

Decontaminating metal surfaces  

DOE Patents [OSTI]

Radioactively contaminated surfaces can be electrolytically decontaminated with greatly increased efficiencies by using electrolytes containing higher than heretofore conventional amounts of nitrate, e.g.,>600 g/l of NaNO.sub.3, or by using nitrate-containing electrolytes which are acidic, e.g., of a pH<6.

Childs, Everett L. (Boulder, CO)

1984-11-06T23:59:59.000Z

177

NNSA and Kazakhstan Complete Operation to Eliminate Highly Enriched...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Kazakhstan Complete Operation to Eliminate Highly Enriched Uranium | National Nuclear Security Administration Facebook Twitter Youtube Flickr RSS People Mission Managing the...

178

Integrated decontamination process for metals  

DOE Patents [OSTI]

An integrated process for decontamination of metals, particularly metals that are used in the nuclear energy industry contaminated with radioactive material. The process combines the processes of electrorefining and melt refining to purify metals that can be decontaminated using either electrorefining or melt refining processes.

Snyder, Thomas S. (Oakmont, PA); Whitlow, Graham A. (Murrysville, PA)

1991-01-01T23:59:59.000Z

179

Feasibility of gas-phase decontamination of gaseous diffusion equipment  

SciTech Connect (OSTI)

The five buildings at the K-25 Site formerly involved in the gaseous diffusion process contain 5000 gaseous diffusion stages as well as support facilities that are internally contaminated with uranium deposits. The gaseous diffusion facilities located at the Portsmouth Gaseous Diffusion Plant and the Paducah Gaseous Diffusion Plant also contain similar equipment and will eventually close. The decontamination of these facilities will require the most cost-effective technology consistent with the criticality, health physics, industrial hygiene, and environmental concerns; the technology must keep exposures to hazardous substances to levels as low as reasonably achievable (ALARA). This report documents recent laboratory experiments that were conducted to determine the feasibility of gas-phase decontamination of the internal surfaces of the gaseous diffusion equipment that is contaminated with uranium deposits. A gaseous fluorinating agent is used to fluorinate the solid uranium deposits to gaseous uranium hexafluoride (UF{sub 6}), which can be recovered by chemical trapping or freezing. The lab results regarding the feasibility of the gas-phase process are encouraging. These results especially showed promise for a novel decontamination approach called the long-term, low-temperature (LTLT) process. In the LTLT process: The equipment is rendered leak tight, evacuated, leak tested, and pretreated, charged with chlorine trifluoride (ClF{sub 3}) to subatmospheric pressure, left for an extended period, possibly > 4 months, while processing other items. Then the UF{sub 6} and other gases are evacuated. The UF{sub 6} is recovered by chemical trapping. The lab results demonstrated that ClF{sub 3} gas at subatmospheric pressure and at {approx} 75{degree}F is capable of volatilizing heavy deposits of uranyl fluoride from copper metal surfaces sufficiently that the remaining radioactive emissions are below limits.

Munday, E.B.; Simmons, D.W.

1993-02-01T23:59:59.000Z

180

Granulated decontamination formulations  

DOE Patents [OSTI]

A decontamination formulation and method of making that neutralizes the adverse health effects of both chemical and biological compounds, especially chemical warfare (CW) and biological warfare (BW) agents, and toxic industrial chemicals. The formulation provides solubilizing compounds that serve to effectively render the chemical and biological compounds, particularly CW and BW compounds, susceptible to attack, and at least one reactive compound that serves to attack (and detoxify or kill) the compound. The formulation includes at least one solubilizing agent, a reactive compound, a sorbent additive, and water. A highly adsorbent sorbent additive (e.g., amorphous silica, sorbitol, mannitol, etc.) is used to "dry out" one or more liquid ingredients into a dry, free-flowing powder that has an extended shelf life, and is more convenient to handle and mix in the field.

Tucker, Mark D. (Albuquerque, NM)

2007-10-02T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


181

Decontamination & decommissioning focus area  

SciTech Connect (OSTI)

In January 1994, the US Department of Energy Office of Environmental Management (DOE EM) formally introduced its new approach to managing DOE`s environmental research and technology development activities. The goal of the new approach is to conduct research and development in critical areas of interest to DOE, utilizing the best talent in the Department and in the national science community. To facilitate this solutions-oriented approach, the Office of Science and Technology (EM-50, formerly the Office of Technology Development) formed five Focus AReas to stimulate the required basic research, development, and demonstration efforts to seek new, innovative cleanup methods. In February 1995, EM-50 selected the DOE Morgantown Energy Technology Center (METC) to lead implementation of one of these Focus Areas: the Decontamination and Decommissioning (D & D) Focus Area.

NONE

1996-08-01T23:59:59.000Z

182

Decontaminating lead bricks and shielding  

SciTech Connect (OSTI)

Lead used for shielding is often surface contaminated with radioisotopes and is therefore a RCRA D008 mixed waste. The technology-based standard for treatment is macroencapsulation. However, decontaminating and recycling the clean lead is a more attractive solution. Los Alamos National Laboratory decontaminates material and equipment contaminated with radioisotopes. Decontaminating lead poses special problems because of the RCRA hazard classification and the size of the inventory, now about 50 tons and likely to grow substantially because of planned decommissioning operations. This lead, in the form of bricks and other shield shapes, is surface contaminated with fission products. One of the best methods for decontaminating lead is removing the thin superficial layer of contamination with an abrasive medium trader pressure. For lead, a mixture of alumina with water and air at about 40 psig rapidly and effectively decontaminates the lead. The abrasive medium is sprayed onto the lead in a sealed-off area. The slurry of abrasive and particles of lead falls through a floor grating and is collected in a sump. A pump sends the slurry mixture back to the spray gun, creating a continuous process. The process generates small volumes of contaminated lead slurry that can be solidified and, because it passes the TCLP, is not a mixed waste. The decontaminated lead can be released for recycling.

Lussiez, G.W.

1993-05-01T23:59:59.000Z

183

Decontaminating lead bricks and shielding  

SciTech Connect (OSTI)

Lead used for shielding is often surface contaminated with radioisotopes and is therefore a RCRA D008 mixed waste. The technology-based standard for treatment is macroencapsulation. However, decontaminating and recycling the clean lead is a more attractive solution. Los Alamos National Laboratory decontaminates material and equipment contaminated with radioisotopes. Decontaminating lead poses special problems because of the RCRA hazard classification and the size of the inventory, now about 50 tons and likely to grow substantially because of planned decommissioning operations. This lead, in the form of bricks and other shield shapes, is surface contaminated with fission products. One of the best methods for decontaminating lead is removing the thin superficial layer of contamination with an abrasive medium trader pressure. For lead, a mixture of alumina with water and air at about 40 psig rapidly and effectively decontaminates the lead. The abrasive medium is sprayed onto the lead in a sealed-off area. The slurry of abrasive and particles of lead falls through a floor grating and is collected in a sump. A pump sends the slurry mixture back to the spray gun, creating a continuous process. The process generates small volumes of contaminated lead slurry that can be solidified and, because it passes the TCLP, is not a mixed waste. The decontaminated lead can be released for recycling.

Lussiez, G.W.

1993-01-01T23:59:59.000Z

184

India's Worsening Uranium Shortage  

SciTech Connect (OSTI)

As a result of NSG restrictions, India cannot import the natural uranium required to fuel its Pressurized Heavy Water Reactors (PHWRs); consequently, it is forced to rely on the expediency of domestic uranium production. However, domestic production from mines and byproduct sources has not kept pace with demand from commercial reactors. This shortage has been officially confirmed by the Indian Planning Commission’s Mid-Term Appraisal of the country’s current Five Year Plan. The report stresses that as a result of the uranium shortage, Indian PHWR load factors have been continually decreasing. The Uranium Corporation of India Ltd (UCIL) operates a number of underground mines in the Singhbhum Shear Zone of Jharkhand, and it is all processed at a single mill in Jaduguda. UCIL is attempting to aggrandize operations by establishing new mines and mills in other states, but the requisite permit-gathering and development time will defer production until at least 2009. A significant portion of India’s uranium comes from byproduct sources, but a number of these are derived from accumulated stores that are nearing exhaustion. A current maximum estimate of indigenous uranium production is 430t/yr (230t from mines and 200t from byproduct sources); whereas, the current uranium requirement for Indian PHWRs is 455t/yr (depending on plant capacity factor). This deficit is exacerbated by the additional requirements of the Indian weapons program. Present power generation capacity of Indian nuclear plants is 4350 MWe. The power generation target set by the Indian Department of Atomic Energy (DAE) is 20,000 MWe by the year 2020. It is expected that around half of this total will be provided by PHWRs using indigenously supplied uranium with the bulk of the remainder provided by breeder reactors or pressurized water reactors using imported low-enriched uranium.

Curtis, Michael M.

2007-01-15T23:59:59.000Z

185

New generation enrichment monitoring technology for gas centrifuge enrichment plants  

SciTech Connect (OSTI)

The continuous enrichment monitor, developed and fielded in the 1990s by the International Atomic Energy Agency, provided a go-no-go capability to distinguish between UF{sub 6} containing low enriched (approximately 4% {sup 235}U) and highly enriched (above 20% {sup 235}U) uranium. This instrument used the 22-keV line from a {sup 109}Cd source as a transmission source to achieve a high sensitivity to the UF{sub 6} gas absorption. The 1.27-yr half-life required that the source be periodically replaced and the instrument recalibrated. The instrument's functionality and accuracy were limited by the fact that measured gas density and gas pressure were treated as confidential facility information. The modern safeguarding of a gas centrifuge enrichment plant producing low-enriched UF{sub 6} product aims toward a more quantitative flow and enrichment monitoring concept that sets new standards for accuracy stability, and confidence. An instrument must be accurate enough to detect the diversion of a significant quantity of material, have virtually zero false alarms, and protect the operator's proprietary process information. We discuss a new concept for advanced gas enrichment assay measurement technology. This design concept eliminates the need for the periodic replacement of a radioactive source as well as the need for maintenance by experts. Some initial experimental results will be presented.

Ianakiev, Kiril D [Los Alamos National Laboratory; Alexandrov, Boian S. [Los Alamos National Laboratory; Boyer, Brian D. [Los Alamos National Laboratory; Hill, Thomas R. [Los Alamos National Laboratory; Macarthur, Duncan W. [Los Alamos National Laboratory; Marks, Thomas [Los Alamos National Laboratory; Moss, Calvin E. [Los Alamos National Laboratory; Sheppard, Gregory A. [Los Alamos National Laboratory; Swinhoe, Martyn T. [Los Alamos National Laboratory

2008-06-13T23:59:59.000Z

186

Decontaminating lead bricks and shielding  

SciTech Connect (OSTI)

Lead used for shielding is often surface contaminated with radioisotopes and is therefore a RCRA D008 mixed waste. The technology-based standard for treatment is macroencapsulation. However, decontaminating and recycling the clean lead is a more attractive solution. Los Alamos National Laboratory decontaminates material and equipment contaminated with radioisotopes. Decontaminating lead poses special problems because of the RCRA hazard classification and the size of the inventory, now about 50 tons and likely to grow substantially of planned decommissioning operations. Thus lead, in the form of bricks and other shield shapes, is surface contaminated with fission products. One of the best methods for contaminated lead is removing the superficial layer of contamination with an abrasive medium under pressure. For lead, a mixture of alumina with water and air at about 40 psig rapidly and effectively decontaminates the lead. The abrasive medium is sprayed onto the lead in a scaled-off area. The slurry of abrasive and particles of lead falls through a floor and is collected in a sump. A pump sends the slurry mixture back to the spray gun, creating a continuous process. The process generates small volumes of lead slurry that can be solidified and, because it passes the TCLP, is not a mixed waste. The decontaminated lead can be released for recycling.

Lussiez, G.

1994-02-01T23:59:59.000Z

187

Decontamination and decommissioning of the Mayaguez (Puerto Rico) facility  

SciTech Connect (OSTI)

On February 6, 1987 the US Department of Energy (DOE) awarded the final phase of the decontamination and decommissioning of the nuclear and reactor facilities at the Center for Energy and Environmental Research (CEER), in Mayaguez, Puerto Rico. Bechtel National, Inc., was made the decontamination and decommissioning (D and D) contractor. The goal of the project was to enable DOE to proceed with release of the CEER facility for use by the University of Puerto Rico, who was the operator. This presentation describes that project and lesson learned during its progress. The CEER facility was established in 1957 as the Puerto Rico Nuclear Center, a part of the Atoms for Peace Program. It was a nuclear training and research institution with emphasis on the needs of Latin America. It originally consisted of a 1-megawatt Materials Testing Reactor (MTR), support facilities and research laboratories. After eleven years of operation the MTR was shutdown and defueled. A 2-megawatt TRIGA reactor was installed in 1972 and operated until 1976, when it woo was shutdown. Other radioactive facilities at the center included a 10-watt homogeneous L-77 training reactor, a natural uranium graphite-moderated subcritical assembly, a 200KV particle accelerator, and a 15,000 Ci Co-60 irradiation facility. Support facilities included radiochemistry laboratories, counting rooms and two hot cells. As the emphasis shifted to non-nuclear energy technology a name change resulted in the CEER designation, and plans were started for the decontamination and decommissioning effort.

Jackson, P.K.; Freemerman, R.L. [Bechtel National, Inc., Oak Ridge, TN (United States)

1989-11-01T23:59:59.000Z

188

Microbial Janitors: Enabling natural microbes to clean up uranium contamination  

E-Print Network [OSTI]

Microbial Janitors: Enabling natural microbes to clean up uranium contamination Oak Ridge to the development of the atomic bomb. Uranium enrichment activities on the Oak Ridge Reservation in the 1940s until then the uranium and nitrate contamination has spread through the ground and now covers an area of about 7 km

189

Disposition of Surplus Highly Enriched Uranium  

Broader source: Energy.gov (indexed) [DOE]

project, The impacts from normal (accident-free) transportation, inclu- ding handling and air pollution would be about 1,9x10-2 fatalities. The combined impact for the total...

190

Disposition of Surplus Highly Enriched Uranium  

Broader source: Energy.gov (indexed) [DOE]

dose calculated by GENH. Latent cancer fatalities were calculated by applying this dose to all workers assuming that they are located 1,000 m away (or at the site bounda if...

191

Disposition of Surplus Highly Enriched Uranium  

Broader source: Energy.gov (indexed) [DOE]

fuel or the blending of HEU to LEU as metal. Under dl blending dtematives, the maximum radiation dose to the maximy exposed individual of the public is 2.0 millirem (mrem)...

192

Uranium Mining, Conversion, and Enrichment Industries  

Broader source: Energy.gov (indexed) [DOE]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) "ofEarly Career Scientists' Research Petroleum ReserveDepartment ofEnergy,Potomac RiverNiketa KumarUraniumi

193

Rehabilitation of contaminated territories while liquidating enterprises of uranium mining industry of the CIS  

SciTech Connect (OSTI)

Uranium mining in the Russian Federation has caused contamination of the environment with solid, liquid and gaseous wastes. Radioactive materials are being leached from residual uranium ores and mill tailings piles. These contaminated areas are being decontaminated and recultivated. Ensuring radiation safety in remediating is of prime importance.

Karamushka, V.P.; Ostroborodov, V.V. [VNIPIPROMTECHNOLOGII, Moscow (Russian Federation)

1993-12-31T23:59:59.000Z

194

Ultrafiltration evaluation with depleted uranium oxide  

SciTech Connect (OSTI)

Scientists at the Los Alamos National Laboratory Plutonium Facility are using electrodissolution in neutral to alkaline solutions to decontaminate oralloy parts that have surface plutonium contamination. Ultrafiltration of the electrolyte stream removes precipitate so that the electrolyte stream to the decontamination fixture is precipitate free. This report describes small-scale laboratory ultrafiltration experiments that the authors performed to determine conditions necessary for full-scale operation of an ultrafiltration module. Performance was similar to what they observed in the ferric hydroxide system. At 12 psi transmembrane pressure, a shear rate of 12,000 sec{sup {minus}1} was sufficient to sustain membrane permeability. Ultrafiltration of uranium(VI) oxide appears to occur as easily as ultrafiltration of ferric hydroxide. Considering the success reported in this study, the authors plan to add ultrafiltration to the next decontamination system for oralloy parts.

Weisbrod, K.R.; Schake, A.R.; Morgan, A.N.; Purdy, G.M.; Martinez, H.E.; Nelson, T.O.

1998-03-01T23:59:59.000Z

195

Heterogeneous modeling of the uranium in situ recovery: Kinetic versus solubility Jrmy. Nosa,1, 2  

E-Print Network [OSTI]

Heterogeneous modeling of the uranium in situ recovery: Kinetic versus solubility control Jérémy Mines, Tour AREVA, 1 place Jean Millier, 92084 Paris La Défense Cedex, France The uranium in situ, into the deposit to selectively dissolve uranium. The solution enriched in uranium is pumped out and processed

Boyer, Edmond

196

Proceedings of the 1988 International Meeting on Reduced Enrichment for Research and Test Reactors  

SciTech Connect (OSTI)

The international effort to develop and implement new research reactor fuels utilizing low-enriched uranium, instead of highly- enriched uranium, continues to make solid progress. This effort is the cornerstone of a widely shared policy aimed at reducing, and possibly eliminating, international traffic in highly-enriched uranium and the nuclear weapon proliferation concerns associated with this traffic. To foster direct communication and exchange of ideas among the specialists in this area, the Reduced Enrichment Research and Test Reactor (RERTR) Program, at Argonne National Laboratory, sponsored this meeting as the eleventh of a series which began 1978. Individual papers presented at the meeting have been cataloged separately.

Not Available

1993-07-01T23:59:59.000Z

197

Concrete decontamination by Electro-Hydraulic Scabbling (EHS). Topical report  

SciTech Connect (OSTI)

Electro-Hydraulic Scabbling (EHS) technology and equipment for decontaminating concrete structures from radionuclides, organic substances, and hazardous metals is being developed by Textron Systems Division (TSD). This wet scabbling technique involves the generation of powerful shock waves and intense cavitation by a strong pulsed electric discharge in a water layer at the concrete surface. The high pressure impulse results in stresses which crack and peel off a concrete layer of a controllable thickness. Scabbling produces contaminated debris of relatively small volume which can be easily removed, leaving clean bulk concrete. This new technology is being developed under Contract No. DE-AC21-93MC30164. The project objective is to develop and demonstrate a cost-efficient, rapid, controllable process to remove the surface layer of contaminated concrete while generating minimal secondary waste. The primary target of this program is uranium-contaminated concrete floors which constitute a substantial part of the contaminated area at DOE weapon facilities.

NONE

1996-03-30T23:59:59.000Z

198

INTEGRATED VERTICAL AND OVERHEAD DECONTAMINATION SYSTEM  

SciTech Connect (OSTI)

This report summarizes the activities performed during FY98 and describes the planned activities for FY99. Accomplishments for FY98 include identifying and selecting decontamination, the screening of potential characterization technologies, development of minimum performance factors for the decontamination technology, and development and identification of Applicable, Relevant and Appropriate Regulations (ARARs).

M.A. Ebadian, Ph.D.

1999-01-01T23:59:59.000Z

199

Composition of the U.S. DOE Depleted Uranium Inventory  

E-Print Network [OSTI]

about 2.75 wt% U-235. For further enrichment, the material was shipped to the Oak Ridge and Portsmouth plants. In addition to natural uranium, also uranium recycled from spent fuel was fed into the Paducah enrichment cascade (Table 2 and Fig. 2). The recycled uranium introduced various isotopes not found in natural uranium into the cascade: fission products, such as Technetium-99; transuranics, such as Neptunium-237 and Plutonium-239; and the artificial uranium isotope of Uranium-236. The spent fuel, from which uranium was recycled, originated from the Hanford and Savannah River military plutonium production reactors. This uranium was recycled, although its assay of U-235 was somewhat lower than in natural uranium (Table 2). This obviously must be seen in the context of the Cold War era, when uranium was a scarce resource. Due to the low burn-up of the military reactors, concentrations of artificial U-236 are comparatively low in this recycled uranium. The recycled uranium represents

Concentration Of Less

200

Uranium from seawater  

SciTech Connect (OSTI)

A novel process for recovering uranium from seawater is proposed and some of the critical technical parameters are evaluated. The process, in summary, consists of two different options for contacting adsorbant pellets with seawater without pumping the seawater. It is expected that this will reduce the mass handling requirements, compared to pumped seawater systems, by a factor of approximately 10/sup 5/, which should also result in a large reduction in initial capital investment. Activated carbon, possibly in combination with a small amount of dissolved titanium hydroxide, is expected to be the preferred adsorbant material instead of the commonly assumed titanium hydroxide alone. The activated carbon, after exposure to seawater, can be stripped of uranium with an appropriate eluant (probably an acid) or can be burned for its heating value (possible in a power plant) leaving the uranium further enriched in its ash. The uranium, representing about 1% of the ash, is then a rich ore and would be recovered in a conventional manner. Experimental results have indicated that activated carbon, acting alone, is not adequately effective in adsorbing the uranium from seawater. We measured partition coefficients (concentration ratios) of approximately 10/sup 3/ in seawater instead of the reported values of 10/sup 5/. However, preliminary tests carried out in fresh water show considerable promise for an extraction system that uses a combination of dissolved titanium hydroxide (in minute amounts) which forms an insoluble compound with the uranyl ion, and the insoluble compound then being sorbed out on activated carbon. Such a system showed partition coefficients in excess of 10/sup 5/ in fresh water. However, the system was not tested in seawater.

Gregg, D.; Folkendt, M.

1982-09-21T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


201

The ultimate disposition of depleted uranium  

SciTech Connect (OSTI)

Depleted uranium (DU) is produced as a by-product of the uranium enrichment process. Over 340,000 MTU of DU in the form of UF{sub 6} have been accumulated at the US government gaseous diffusion plants and the stockpile continues to grow. An overview of issues and objectives associated with the inventory management and the ultimate disposition of this material is presented.

Lemons, T.R. [Uranium Enrichment Organization, Oak Ridge, TN (United States)

1991-12-31T23:59:59.000Z

202

Summary of decontamination cover manufacturing experience  

SciTech Connect (OSTI)

Decontamination cover forming cracks and vent cup assembly leaks through the decontamination covers were early manufacturing problems. The decontamination cover total manufacturing process yield was as low as 55%. Applicable tooling and procedures were examined. All manufacturing steps from foil fabrication to final assembly leak testing were considered as possible causes or contributing factors to these problems. The following principal changes were made to correct these problems: (1) the foil annealing temperature was reduced from 1375{degrees} to 1250{degrees}C, (2) the decontamination cover fabrication procedure (including visual inspection for surface imperfections and elimination of superfluous operations) was improved, (3) the postforming dye penetrant inspection procedure was revised for increased sensitivity, (4) a postforming (prewelding) 1250{degrees}C/1 h vacuum stress-relief operation was added, (5) a poststress relief (prewelding) decontamination cover piece-part leak test was implemented, (6) the hold-down fixture used during the decontamination cover-to-cup weld was modified, and concomitantly, and (7) the foil fabrication process was changed from the extruding and rolling of 63-mm-diam vacuum arc-remelted ingots (extrusion process) to the rolling of 19-mm-square arc-melted drop castings (drop cast process). Since these changes were incorporated, the decontamination cover total manufacturing process yield has been 91 %. Most importantly, more than 99% of the decontamination covers welded onto vent cup assemblies were acceptable. The drastic yield improvement is attributed primarily to the change in the foil annealing temperature from 1375{degrees} to 1250{degrees}C and secondarily to the improvements in the decontamination cover fabrication procedure.

Ulrich, G.B.; Berry, H.W.

1995-02-01T23:59:59.000Z

203

Deactivation, Decontamination and Decommissioning Project Summaries  

SciTech Connect (OSTI)

This report is a compilation of summary descriptions of Deactivation, Decontamination and Decommissioning, and Surveillance and Maintenance projects planned for inactive facilities and sites at the INEEL from FY-2002 through FY-2010. Deactivations of contaminated facilities will produce safe and stable facilities requiring minimal surveillance and maintenance pending further decontamination and decommissioning. Decontamination and decommissioning actions remove contaminated facilities, thus eliminating long-term surveillance and maintenance. The projects are prioritized based on risk to DOE-ID, the public, and the environment, and the reduction of DOE-ID mortgage costs and liability at the INEEL.

Peterson, David Shane; Webber, Frank Laverne

2001-07-01T23:59:59.000Z

204

Decontamination formulation with sorbent additive  

DOE Patents [OSTI]

A decontamination formulation and method of making that neutralizes the adverse health effects of both chemical and biological compounds, especially chemical warfare (CW) and biological warfare (BW) agents, and toxic industrial chemicals. The formulation provides solubilizing compounds that serve to effectively render the chemical and biological compounds, particularly CW and BW compounds, susceptible to attack, and at least one reactive compound that serves to attack (and detoxify or kill) the compound. The formulation includes at least one solubilizing agent, a reactive compound, a bleaching activator, a sorbent additive, and water. The highly adsorbent, water-soluble sorbent additive (e.g., sorbitol or mannitol) is used to "dry out" one or more liquid ingredients, such as the liquid bleaching activator (e.g., propylene glycol diacetate or glycerol diacetate) and convert the activator into a dry, free-flowing powder that has an extended shelf life, and is more convenient to handle and mix in the field.

Tucker; Mark D. (Albuquerque, NM), Comstock; Robert H. (Gardendale, AL)

2007-10-16T23:59:59.000Z

205

Uranium industry annual 1997  

SciTech Connect (OSTI)

This report provides statistical data on the U.S. uranium industry`s activities relating to uranium raw materials and uranium marketing.

NONE

1998-04-01T23:59:59.000Z

206

URANIUM IN ALKALINE ROCKS  

E-Print Network [OSTI]

Greenland," in Uranium Exploration Geology, Int. AtomicOklahoma," 1977 Nure Geology Uranium Symposium, Igneous HostMcNeil, M. , 1977. "Geology of Brazil's Uranium and Thorium

Murphy, M.

2011-01-01T23:59:59.000Z

207

Y-12 Uranium Exposure Study  

SciTech Connect (OSTI)

Following the recent restart of operations at the Y-12 Plant, the Radiological Control Organization (RCO) observed that the enriched uranium exposures appeared to involve insoluble rather than soluble uranium that presumably characterized most earlier Y-12 operations. These observations necessitated changes in the bioassay program, particularly the need for routine fecal sampling. In addition, it was not reasonable to interpret the bioassay data using metabolic parameter values established during earlier Y-12 operations. Thus, the recent urinary and fecal bioassay data were interpreted using the default guidance in Publication 54 of the International Commission on Radiological Protection (ICRP); that is, inhalation of Class Y uranium with an activity median aerodynamic diameter (AMAD) of 1 {micro}m. Faced with apparently new workplace conditions, these actions were appropriate and ensured a cautionary approach to worker protection. As additional bioassay data were accumulated, it became apparent that the data were not consistent with Publication 54. Therefore, this study was undertaken to examine the situation.

Eckerman, K.F.; Kerr, G.D.

1999-08-05T23:59:59.000Z

208

The geochemistry of uranium in the Orca Basin  

E-Print Network [OSTI]

no uranium enrichment, with concentrations ranging from 2. 1 to 4. gppm, reflective of normal Gulf of Mexico sediments. This is the result of two dominant processes operating within the basin. First, the sharp pycnocline at the brine/seawater interface... . . . . . . . . , . . . , 37 xi Figure Page 16 Ores Basin Seismic Reflection Profile A 40 17 Ores Basin Seismic Reflection Profile B 42 18 Proposed Mechanism of Uranium Uptake in the Atlantis II Deep 59 INTRODUCTION Economic Status of Uranium in the United States...

Weber, Frederick Fewell

1979-01-01T23:59:59.000Z

209

Urban Decontamination Experience at Pripyat Ukraine - 13526  

SciTech Connect (OSTI)

This paper describes the efficiency of radioactive decontamination activities of the urban landscape in the town of Pripyat, Ukraine. Different methods of treatment for various urban infrastructure and different radioactive contaminants are assessed. Long term changes in the radiation condition of decontaminated urban landscapes are evaluated: 1. Decontamination of the urban system requires the simultaneous application of multiple methods including mechanical, chemical, and biological. 2. If a large area has been contaminated, decontamination of local areas of a temporary nature. Over time, there is a repeated contamination of these sites due to wind transport from neighboring areas. 3. Involvement of earth-moving equipment and removal of top soil by industrial method achieves 20-fold reduction in the level of contamination by radioactive substances, but it leads to large amounts of waste (up to 1500 tons per hectare), and leads to the re-contamination of treated areas due to scatter when loading, transport pollutants on the wheels of vehicles, etc.. (authors)

Paskevych, Sergiy [Institute for Safety Problems of Nuclear Power Plants, National Academy of Sciences of Ukraine, 36 a Kirova str. Chornobyl, Kiev region, 07200 (Ukraine)] [Institute for Safety Problems of Nuclear Power Plants, National Academy of Sciences of Ukraine, 36 a Kirova str. Chornobyl, Kiev region, 07200 (Ukraine); Voropay, Dmitry [Federal State Unitary Enterprise 'Russian State Center of Inventory and Registration and Real Estate - Federal Bureau of Technical Inventory', 37-2 Bernadsky Prospekt, Moscow Russia 119415 (Russian Federation)] [Federal State Unitary Enterprise 'Russian State Center of Inventory and Registration and Real Estate - Federal Bureau of Technical Inventory', 37-2 Bernadsky Prospekt, Moscow Russia 119415 (Russian Federation); Schmieman, Eric [Battelle Memorial Institute, PO Box 999 MSIN K6-90, Richland, WA 99352 (United States)] [Battelle Memorial Institute, PO Box 999 MSIN K6-90, Richland, WA 99352 (United States)

2013-07-01T23:59:59.000Z

210

Enclosure 1 -CCP-AK-INL-004, Table 5-2 (1 page) Table 5-2. Isotopic Compositions of Rocky Flats Plutonium and Uranium  

E-Print Network [OSTI]

Flats Plutonium and Uranium Weapons-Grade Plutonium Enriched Uranium Depleted Uranium Plutonium-238 0.01 ­ 0.05% Uranium-234 0.1 ­ 1.02% Uranium-234 0.0006% Plutonium-239 92.8 ­ 94.4% Uranium-235 90 ­ 94% Uranium-235 0.2 ­ 0.3% Plutonium-240 4.85 ­ 6.5% Uranium-236 0.4 ­ 0.5% Uranium-238 99.7 ­ 99.8% Plutonium

211

Nuclear reactor cooling system decontamination reagent regeneration  

DOE Patents [OSTI]

An improved method for decontaminating the coolant system of water-cooled nuclear power reactors and for regenerating the decontamination solution. A small amount of one or more weak-acid organic complexing agents is added to the reactor coolant, and the pH is adjusted to form a decontamination solution which is circulated throughout the coolant system to dissolve metal oxides from the interior surfaces and complex the resulting metal ions and radionuclide ions. The coolant containing the complexed metal ions and radionuclide ions is passed through a strong-base anion exchange resin bed which has been presaturated with a solution containing the complexing agents in the same ratio and having the same pH as the decontamination solution. As the decontamination solution passes through the resin bed, metal-complexed anions are exchanged for the metal-ion-free anions on the bed, while metal-ion-free anions in the solution pass through the bed, thus removing the metal ions and regenerating the decontamination solution.

Anstine, Larry D. (San Jose, CA); James, Dean B. (Saratoga, CA); Melaika, Edward A. (Berkeley, CA); Peterson, Jr., John P. (Livermore, CA)

1985-01-01T23:59:59.000Z

212

EIS-0359: Uranium Hexafluoride Conversion Facility at the Paducah, Kentucky Site  

Broader source: Energy.gov [DOE]

This site-specific EIS considers the construction, operation, maintenance, and decontamination and decommissioning of the proposed depleted uranium hexafluoride (DUF6) conversion facility at three locations within the Paducah site; transportation of depleted uranium conversion products and waste materials to a disposal facility; transportation and sale of the hydrogen fluoride (HF) produced as a conversion co-product; and neutralization of HF to calcium fluoride and its sale or disposal in the event that the HF product is not sold.

213

RERTR 2009 (Reduced Enrichment for Research and Test Reactors)  

SciTech Connect (OSTI)

The U.S. Department of Energy/National Nuclear Security Administration's Office of Global Threat Reduction in cooperation with the China Atomic Energy Authority and International Atomic Energy Agency hosted the 'RERTR 2009 International Meeting on Reduced Enrichment for Research and Test Reactors.' The meeting was organized by Argonne National Laboratory, China Institute of Atomic Energy and Idaho National Laboratory and was held in Beijing, China from November 1-5, 2009. This was the 31st annual meeting in a series on the same general subject regarding the conversion of reactors within the Global Threat Reduction Initiative (GTRI). The Reduced Enrichment for Research and Test Reactors (RERTR) Program develops technology necessary to enable the conversion of civilian facilities using high enriched uranium (HEU) to low enriched uranium (LEU) fuels and targets.

Totev, T.; Stevens, J.; Kim, Y. S.; Hofman, G.; Matos, J.; Hanan, N.; Garner, P.; Dionne, B.; Olson, A.; Feldman, E.; Dunn, F.; Nuclear Engineering Division; Atomic Research Center; Inst. of Nuclear Physics; LLNL; INL; Korea Atomic Energy Research Inst.; Comisi?n Nacional de Energ?a At?mica; Nuclear Reactor Lab.; Inst. of Atomic Energy-Poland; AECL-Canada; Hungarian Academy of Sciences KFKI Atomic Energy Research Inst.; Japan Atomic Energy Agency; Nuclear Power Inst. of China; Kyoto Univ. Research Reactor Inst.

2010-03-01T23:59:59.000Z

214

Mechanical decontamination techniques for floor drain systems  

SciTech Connect (OSTI)

The unprecedented nature of cleanup activities at Three Mile Island Unit 2 (TMI-2) following the 1979 accident has necessitated the development of new techniques to deal with radiation and contamination in the plant. One of these problems was decontamination of floor drain systems, which had become highly contaminated with various forms of dirt and sludge containing high levels of fission products and fuel from the damaged reactor core. The bulk of this contamination is loosely adherent to the drain pipe walls; however, significant amounts of contamination have become incorporated into pipe wall oxide and corrosion layers and embedded in microscopic pits and fissures in the pipe wall material. The need to remove this contamination was recognized early in the TMI-2 cleanup effort. A program consisting of development and laboratory testing of floor drain decontamination techniques was undertaken early in the cleanup with support from the Electric Power Research Institute (EPRI). Based on this initial research, two techniques were judged to show promise for use at TMI-2: a rotating brush hone system and a high-pressure water mole nozzle system. Actual use of these devices to clean floor drains at TMI-2 has yielded mixed decontamination results. The decontamination effectiveness that has been obtained is highly dependent on the nature of the contamination in the drain pipe and the combination of decontamination techniques used.

Palau, G.L.; Saigusa, Moriyuki

1987-01-01T23:59:59.000Z

215

Effect of reduced enrichment on the fuel cycle for research reactors  

SciTech Connect (OSTI)

The new fuels developed by the RERTR Program and by other international programs for application in research reactors with reduced uranium enrichment (<20% EU) are discussed. It is shown that these fuels, combined with proper fuel-element design and fuel-management strategies, can provide at least the same core residence time as high-enrichment fuels in current use, and can frequently significantly extend it. The effect of enrichment reduction on other components of the research reactor fuel cycle, such as uranium and enrichment requirements, fuel fabrication, fuel shipment, and reprocessing are also briefly discussed with their economic implications. From a systematic comparison of HEU and LEU cores for the same reference research reactor, it is concluded that the new fuels have a potential for reducing the research reactor fuel cycle costs while reducing, at the same time, the uranium enrichment of the fuel.

Travelli, A.

1982-01-01T23:59:59.000Z

216

Draft Environmental Impact Statement for Construction and Operation of a Depleted Uranium Hexafluoride Conversion Facility at the Portsmouth, Ohio, Site  

SciTech Connect (OSTI)

This document is a site-specific environmental impact statement (EIS) for construction and operation of a proposed depleted uranium hexafluoride (DUF{sub 6}) conversion facility at the U.S. Department of Energy (DOE) Portsmouth site in Ohio (Figure S-1). The proposed facility would convert the DUF{sub 6} stored at Portsmouth to a more stable chemical form suitable for use or disposal. The facility would also convert the DUF{sub 6} from the East Tennessee Technology Park (ETTP) site near Oak Ridge, Tennessee. In a Notice of Intent (NOI) published in the Federal Register on September 18, 2001 (Federal Register, Volume 66, page 48123 [66 FR 48123]), DOE announced its intention to prepare a single EIS for a proposal to construct, operate, maintain, and decontaminate and decommission two DUF{sub 6} conversion facilities at Portsmouth, Ohio, and Paducah, Kentucky, in accordance with the National Environmental Policy Act of 1969 (NEPA) (United States Code, Title 42, Section 4321 et seq. [42 USC 4321 et seq.]) and DOE's NEPA implementing procedures (Code of Federal Regulations, Title 10, Part 1021 [10 CFR Part 1021]). Subsequent to award of a contract to Uranium Disposition Services, LLC (hereafter referred to as UDS), Oak Ridge, Tennessee, on August 29, 2002, for design, construction, and operation of DUF{sub 6} conversion facilities at Portsmouth and Paducah, DOE reevaluated its approach to the NEPA process and decided to prepare separate site-specific EISs. This change was announced in a Federal Register Notice of Change in NEPA Compliance Approach published on April 28, 2003 (68 FR 22368); the Notice is included as Attachment B to Appendix C of this EIS. This EIS addresses the potential environmental impacts from the construction, operation, maintenance, and decontamination and decommissioning (D&D) of the proposed conversion facility at three alternative locations within the Portsmouth site; from the transportation of all ETTP cylinders (DUF{sub 6}, low-enriched UF6 [LEU-UF{sub 6}], and empty) to Portsmouth; from the transportation of depleted uranium conversion products to a disposal facility; and from the transportation, sale, use, or disposal of the fluoride-containing conversion products (hydrogen fluoride [HF] or calcium fluoride [CaF{sub 2}]). An option of shipping the ETTP cylinders to Paducah is also considered. In addition, this EIS evaluates a no action alternative, which assumes continued storage of DUF{sub 6} in cylinders at the Portsmouth and ETTP sites. A separate EIS (DOE/EIS-0359) evaluates potential environmental impacts for the proposed Paducah conversion facility.

N /A

2003-11-28T23:59:59.000Z

217

Draft Environmental Impact Statement for Construction and Operation of a Depleted Uranium Hexafluoride Conversion Facility at the Paducah, Kentucky, Site  

SciTech Connect (OSTI)

This document is a site-specific environmental impact statement (EIS) for construction and operation of a proposed depleted uranium hexafluoride (DUF{sub 6}) conversion facility at the U.S. Department of Energy (DOE) Paducah site in northwestern Kentucky (Figure S-1). The proposed facility would convert the DUF{sub 6} stored at Paducah to a more stable chemical form suitable for use or disposal. In a Notice of Intent (NOI) published in the ''Federal Register'' (FR) on September 18, 2001 (''Federal Register'', Volume 66, page 48123 [66 FR 48123]), DOE announced its intention to prepare a single EIS for a proposal to construct, operate, maintain, and decontaminate and decommission two DUF{sub 6} conversion facilities at Portsmouth, Ohio, and Paducah, Kentucky, in accordance with the National Environmental Policy Act of 1969 (NEPA) (''United States Code'', Title 42, Section 4321 et seq. [42 USC 4321 et seq.]) and DOE's NEPA implementing procedures (''Code of Federal Regulations'', Title 10, Part 1021 [10 CFR Part 1021]). Subsequent to award of a contract to Uranium Disposition Services, LLC (hereafter referred to as UDS), Oak Ridge, Tennessee, on August 29, 2002, for design, construction, and operation of DUF{sub 6} conversion facilities at Portsmouth and Paducah, DOE reevaluated its approach to the NEPA process and decided to prepare separate site-specific EISs. This change was announced in a ''Federal Register'' Notice of Change in NEPA Compliance Approach published on April 28, 2003 (68 FR 22368); the Notice is included as Attachment B to Appendix C of this EIS. This EIS addresses the potential environmental impacts from the construction, operation, maintenance, and decontamination and decommissioning (D&D) of the proposed conversion facility at three alternative locations within the Paducah site; from the transportation of depleted uranium conversion products to a disposal facility; and from the transportation, sale, use, or disposal of the fluoride-containing conversion products (hydrogen fluoride [HF] or calcium fluoride [CaF{sub 2}]). Although not part of the proposed action, an option of shipping all cylinders (DUF{sub 6}, low-enriched UF{sub 6} [LEU-UF{sub 6}], and empty) stored at the East Tennessee Technology Park (ETTP) near Oak Ridge, Tennessee, to Paducah rather than to Portsmouth is also considered. In addition, this EIS evaluates a no action alternative, which assumes continued storage of DUF{sub 6} in cylinders at the Paducah site. A separate EIS (DOE/EIS-0360) evaluates the potential environmental impacts for the proposed Portsmouth conversion facility.

N /A

2003-11-28T23:59:59.000Z

218

DECONTAMINATION AND BENEFICIAL USE OF DREDGED MATERIALS.  

SciTech Connect (OSTI)

Our group is leading a large-sale demonstration of dredged material decontamination technologies for the New York/New Jersey Harbor. The goal of the project is to assemble a complete system for economic transformation of contaminated dredged material into an environmentally-benign material used in the manufacture of a variety of beneficial use products. This requires the integration of scientific, engineering, business, and policy issues on matters that include basic knowledge of sediment properties, contaminant distribution visualization, sediment toxicity, dredging and dewatering techniques, decontamination technologies, and product manufacturing technologies and marketing. A summary of the present status of the system demonstrations including the use of both existing and new manufacturing facilities is given here. These decontamination systems should serve as a model for use in dredged material management plans of regions other than NY/NJ Harbor, such as Long Island Sound, where new approaches to the handling of contaminated sediments are desirable.

STERN, E.A.; LODGE, J.; JONES, K.W.; CLESCERI, N.L.; FENG, H.; DOUGLAS, W.S.

2000-12-03T23:59:59.000Z

219

Decontamination, decommissioning, and vendor advertorial issue, 2007  

SciTech Connect (OSTI)

The focus of the July-August issue is on Decontamination, decommissioning, and vendor advertorials. Major articles/reports in this issue include: An interesting year ahead of us, by Tom Christopher, AREVA NP Inc.; U.S.-India Civil Nuclear Cooperation; Decontamination and recycling of retired components, by Sean P. Brushart, Electric Power Research Institute; and, ANO is 33 and going strong, by Tyler Lamberts, Entergy Nuclear Operations, Inc. The industry innovation article is: Continuous improvement process, by ReNae Kowalewski, Arkansas Nuclear One.

Agnihotri, Newal (ed.)

2007-07-15T23:59:59.000Z

220

Decontamination of metals using chemical etching  

DOE Patents [OSTI]

The invention relates to chemical etching process for reclaiming contaminated equipment wherein a reduction-oxidation system is included in a solution of nitric acid to contact the metal to be decontaminated and effect reduction of the reduction-oxidation system, and includes disposing a pair of electrodes in the reduced solution to permit passage of an electrical current between said electrodes and effect oxidation of the reduction-oxidation system to thereby regenerate the solution and provide decontaminated equipment that is essentially radioactive contamination-free.

Lerch, Ronald E. (Kennewick, WA); Partridge, Jerry A. (Richland, WA)

1980-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


221

Engineering assessment of inactive uranium mill tailings  

SciTech Connect (OSTI)

The Grand Junction site has been reevaluated in order to revise the October 1977 engineering assessment of the problems resulting from the existence of radioactive uranium mill tailings at Grand Junction, Colorado. This engineering assessment has included the preparation of topographic maps, the performance of core drillings and radiometric measurements sufficient to determine areas and volumes of tailings and radiation exposures of individuals and nearby populations, the investigations of site hydrology and meteorology, and the evaluation and costing of alternative corrective actions. Radon gas released from the 1.9 million tons of tailings at the Grand Junction site constitutes the most significant environmental impact, although windblown tailings and external gamma radiation are also factors. The eight alternative actions presented herein range from millsite and off-site decontamination with the addition of 3 m of stabilization cover material (Option I), to removal of the tailings to remote disposal sites and decontamination of the tailings site (Options II through VIII). Cost estimates for the eight options range from about $10,200,000 for stabilization in-place to about $39,500,000 for disposal in the DeBeque area, at a distance of about 35 mi, using transportation by rail. If transportation to DeBeque were by truck, the cost estimated to be about $41,900,000. Three principal alternatives for the reprocessing of the Grand Junction tailings were examined: (a) heap leaching; (b) treatment at an existing mill; and (c) reprocessing at a new conventional mill constructed for tailings reprocessing. The cost of the uranium recovered would be about $200/lb by heap leach and $150/lb by conventional plant processes. The spot market price for uranium was $25/lb early in 1981. Therefore, reprocessing the tailings for uranium recovery appears not to be economically attractive.

Not Available

1981-07-01T23:59:59.000Z

222

Decontamination Systems Information and Research Program  

SciTech Connect (OSTI)

The following paragraphs comprise the research efforts during the second quarter of 1998 (April 1 - June 30.) These tasks have been granted a continuation until the end of August 1998. This report represents the last technical quarterly report deliverable for the WVU Cooperative Agreement - Decontamination Systems Information and Research Program. Final draft technical reports will be the next submission. During this period, work was completed on the Injection and Circulation of Potable Water Through PVDs on Task 1.6 - Pilot Scale Demonstration of TCE Flushing Through PVDs at the DOE/RMI Extrusion Plant. The data has been evaluated and representative graphs are presented. The plot of Cumulative Injected Volume vs. Cumulative Week Time show the ability to consistently inject through the two center PVDs at a rate of approximately ten (10) gallons per hour. This injection rate was achieved under a static head that varied from five (5) feet to three (3) feet. The plot of Extracted Flow Rate vs. Cumulative Week Time compares the extraction rate with and without the injection of water. The injection operation was continuous for eight hour periods while the extraction operation was executed over a pulsing schedule. Extraction rates as high as forty-five (45) gallons per hour were achieved in conjunction with injection (a 350% increase over no injection.) The retrieved TCE in the liquid phase varied to a considerable degree depending on the pulsing scheme, indicating a significant amount of stripping (volatilization) took place during the extraction process. A field experiment was conducted to confirm this. A liquid sample was obtained using the same vacuum system used in the pad operation and a second liquid sample was taken by a bailer. Analyzation of TCE concentration showed 99.5% volatilization when the vacuum system was used for extraction. This was also confirmed by data from the air monitoring program which indicated that 92%-99% of the retrieved TCE was being transported in the gas phase. Data on the recovered TCE concentration for the pulsing schemes implemented in the field were collected. Based on the TCE concentration in the liquid phase, the optimum schedule for recovery during an extraction only scenario is ?one hour on - seven hours off - one hour on? which allows for the recharging of the groundwater with TCE by the process of diffusion. With injection utilized, the optimum schedule for the operation is ?one hour on - three hours off - one hour on,? which allows for the optimum recovery of TCE in an optimized amount of liquid. Uranium (U) was recovered in conjunction with TCE removal. Although specifically not targeted, the PVDs indiscriminately retrieved the subsurface contaminants on the order of 65-95 pCi/L. The field work was completed on surfactant augmented injection. Circulation and data reduction from this sequence of testing is ongoing.

Echol E. Cook; Tia Maria Beatty

1998-07-01T23:59:59.000Z

223

Chapter 5. Conclusion Uranium, a naturally occurring element, contributes to low levels of natural background radiation in the  

E-Print Network [OSTI]

are extracted from the earth. Protore is mined uranium ore that is not rich enough to meet the market demand conventional open-pit and underground uranium mining include overburden (although most overburden is not necessarily enriched in uranium as is protore), unreclaimed protore, waste rock, evaporites from mine water

224

The non-aqueous chemistry of uranium has been an active area of exploration in recent decades1,2  

E-Print Network [OSTI]

-purity depleted uranium produced as a by-product of nuclear isotope enrichment programmes. The early actinideThe non-aqueous chemistry of uranium has been an active area of exploration in recent decades1 for uranium will be created in part by the quest of researchers to understand the properties and potential

Cai, Long

225

Melting characteristics of the stainless steel generated from the uranium conversion plant  

SciTech Connect (OSTI)

The partition ratio of cerium (Ce) and uranium (U) in the ingot, slag and dust phases has been investigated for the effect of the slag type, slag concentration and basicity in an electric arc melting process. An electric arc furnace (EAF) was used to melt the stainless steel wastes, simulated by uranium oxide and the real wastes from the uranium conversion plant in Korea Atomic Energy Research Institute (KAERI). The composition of the slag former used to capture the contaminants such as uranium, cerium, and cesium during the melt decontamination process generally consisted of silica (SiO{sub 2}), calcium oxide (CaO) and aluminum oxide (Al{sub 2}O{sub 3}). Also, Calcium fluoride (CaF{sub 2} ), nickel oxide (NiO), and ferric oxide (Fe{sub 2}O{sub 3}) were added to provide an increase in the slag fluidity and oxidative potential. Cerium was used as a surrogate for the uranium because the thermochemical and physical properties of cerium are very similar to those of uranium. Cerium was removed from the ingot phase to slag phase by up to 99% in this study. The absorption ratio of cerium was increased with an increase of the amount of the slag former. And the maximum removal of cerium occurred when the basicity index of the slag former was 0.82. The natural uranium (UO{sub 2}) was partitioned from the ingot phase to the slag phase by up to 95%. The absorption of the natural uranium was considerably dependent on the basicity index of the slag former and the composition of the slag former. The optimum condition for the removal of the uranium was about 1.5 for the basicity index and 15 wt% of the slag former. According to the increase of the amount of slag former, the absorption of uranium oxide in the slag phase was linearly increased due to an increase of its capacity to capture uranium oxide within the slag phase. Through experiments with various slag formers, we verified that the slag formers containing calcium fluoride (CaF{sub 2}) and a high amount of silica were more effective for a melt decontamination of stainless steel wastes contaminated with uranium. During the melting tests with stainless steel wastes from the uranium conversion plant(UCP ) in KAERI, we found that the results of the uranium decontamination were very similar to those of the uranium oxide from the melting of stimulated metal wastes. (authors)

Choi, W.K.; Song, P.S.; Oh, W.Z.; Jung, C.H. [Korea Atomic Energy Research Institute (Korea, Republic of); Min, B.Y. [Chungnam National University, 220 Gung-Dong, Yusung-Gu Taejon 305-764 (Korea, Republic of)

2007-07-01T23:59:59.000Z

226

Separation of uranium from technetium in recovery of spent nuclear fuel  

DOE Patents [OSTI]

A method for decontaminating uranium product from the Purex process comprises addition of hydrazine to the product uranyl nitrate stream from the Purex process, which contains hexavalent (UO.sub.2.sup.2+) uranium and heptavalent technetium (TcO.sub.4 -). Technetium in the product stream is reduced and then complexed by the addition of oxalic acid (H.sub.2 C.sub.2 O.sub.4), and the Tc-oxalate complex is readily separated from the uranium by solvent extraction with 30 vol. % tributyl phosphate in n-dodecane.

Friedman, Horace A. (Oak Ridge, TN)

1985-01-01T23:59:59.000Z

227

Separation of uranium from technetium in recovery of spent nuclear fuel  

DOE Patents [OSTI]

A method for decontaminating uranium product from the Purex 5 process comprises addition of hydrazine to the product uranyl nitrate stream from the Purex process, which contains hexavalent (UO/sub 2//sup 2 +/) uranium and heptavalent technetium (TcO/sub 4/-). Technetium in the product stream is reduced and then complexed by the addition of oxalic acid (H/sub 2/C/sub 2/O/sub 4/), and the Tc-oxalate complex is readily separated from the 10 uranium by solvent extraction with 30 vol % tributyl phosphate in n-dodecane.

Friedman, H.A.

1984-06-13T23:59:59.000Z

228

Biotechnology for the decontamination of Metal  

E-Print Network [OSTI]

Laurentian University SNO Science North #12;Problem: Pollution Heavy Metals Aluminium Lead Caesium CalciumBiotechnology for the decontamination of Metal Wastes Professor Vasu D. Appanna PhD Chair Yttrium #12;Accumulation of metals in living systems #12;Biological Effects #12;Adaptation #12;Aluminium

Appanna, Vasu

229

INTEGRATED VERTICAL AND OVERHEAD DECONTAMINATION (IVOD) SYSTEM  

SciTech Connect (OSTI)

The deactivation and decommissioning of 1200 buildings within the U.S. Department of Energy-Office of Environmental Management complex will require the disposition of a large quantity of contaminated concrete and metal surfaces. It has been estimated that 23 million cubic meters of concrete and over 600,000 tons of metal will need disposition. The disposition of such large quantities of material presents difficulties in the area of decontamination and characterization. The final disposition of this large amount of material will take time and money as well as risk to the D&D work force. A single automated system that would decontaminate and characterize surfaces in one step would not only reduce the schedule and decrease cost during D&D operations but would also protect the D&D workers from unnecessary exposures to contaminated surfaces. This report summarizes the activities performed during FY00 and describes the planned activities for FY01. Accomplishments for FY00 include the following: Development and field-testing of characterization system; Completion of Title III design of deployment platform and decontamination unit; In-house testing of deployment platform and decontamination unit; Completion of system integration design; Identification of deployment site; and Completion of test plan document for deployment of IVOD at Rancho Seco nuclear power facility.

M.A. Ebadian, Ph.D.

2001-01-01T23:59:59.000Z

230

Depleted uranium disposal options evaluation  

SciTech Connect (OSTI)

The Department of Energy (DOE), Office of Environmental Restoration and Waste Management, has chartered a study to evaluate alternative management strategies for depleted uranium (DU) currently stored throughout the DOE complex. Historically, DU has been maintained as a strategic resource because of uses for DU metal and potential uses for further enrichment or for uranium oxide as breeder reactor blanket fuel. This study has focused on evaluating the disposal options for DU if it were considered a waste. This report is in no way declaring these DU reserves a ``waste,`` but is intended to provide baseline data for comparison with other management options for use of DU. To PICS considered in this report include: Retrievable disposal; permanent disposal; health hazards; radiation toxicity and chemical toxicity.

Hertzler, T.J.; Nishimoto, D.D.; Otis, M.D. [Science Applications International Corp., Idaho Falls, ID (United States). Waste Management Technology Div.

1994-05-01T23:59:59.000Z

231

Reduced enrichment for research and test reactors: Proceedings  

SciTech Connect (OSTI)

The international effort to develop new research reactor fuel materials and designs based on the use of low-enriched uranium, instead of highly-enriched uranium, has made much progress during the eight years since its inception. To foster direct communication and exchange of ideas among the specialist in this area, the Reduced Enrichment Research and Test Reactor (RERTR) Program, at the Argonne National Laboratory, sponsored this meeting as the ninth of a series which began in 1978. All previous meetings of this series are listed on the facing page. The focus of this meeting was on the LEU fuel demonstration which was in progress at the Oak Ridge Research (ORR) reactor, not far from where the meeting was held. The visit to the ORR, where a silicide LEU fuel with 4.8 g A/cm/sup 3/ was by then in routine use, illustrated how far work has progressed.

Not Available

1988-05-01T23:59:59.000Z

232

Investigation of the low enrichment conversion of the Texas A and M Nuclear Science Center Reactor  

SciTech Connect (OSTI)

The use of highly enriched uranium as a fuel research reactors is of concern due to the possibility of diversion for nuclear weapons applications. The Texas A M TRIGA reactor currently uses 70% enriched uranium in a FLIP (Fuel Life Improvement Program) fuel element manufactured by General Atomics. Thus fuel also contains 1.5 weight percent of erbium as a burnable poison to prolong useful core life. US university reactors that use highly enriched uranium will be required to covert to 20% or less enrichment to satisfy Nuclear Regulatory Commission requirements for the next core loading if the fuel is available. This investigation examined the feasibility of a material alternate to uranium-zirconium hydride for LEU conversion of a TRIGA reactor. This material is a beryllium oxide uranium dioxide based fuel. The theoretical aspects of core physics analyses were examined to assess the potential advantages of the alternative fuel. A basic model was developed for the existing core configuration since it is desired to use the present fuel element grid for the replacement core. The computing approach was calibrated to the present core and then applied to a core of BeO-UO{sub 2} fuel elements. Further calculations were performed for the General Atomics TRIGA low-enriched uranium zirconium hydride fuel.

Reuscher, J.A.

1988-01-01T23:59:59.000Z

233

The development of uranium foil farication technology utilizing twin roll method for Mo-99 irradiation target  

E-Print Network [OSTI]

MDS Nordion in Canada, occupying about 75% of global supply of Mo-99 isotope, has provided the irradiation target of Mo-99 using the rod-type UAl sub x alloys with HEU(High Enrichment Uranium). ANL (Argonne National Laboratory) through co-operation with BATAN in Indonesia, leading RERTR (Reduced Enrichment for Research and Test Reactors) program substantially for nuclear non-proliferation, has designed and fabricated the annular cylinder of uranium targets, and successfully performed irradiation test, in order to develop the fabrication technology of fission Mo-99 using LEU(Low Enrichment Uranium). As the uranium foils could be fabricated in laboratory scale, not in commercialized scale by hot rolling method due to significant problems in foil quality, productivity and economic efficiency, attention has shifted to the development of new technology. Under these circumstances, the invention of uranium foil fabrication technology utilizing twin-roll casting method in KAERI is found to be able to fabricate LEU or...

Kim, C K; Park, H D

2002-01-01T23:59:59.000Z

234

EIS-0111: Remedial Actions at the Former Vanadium Corporation of America Uranium Mill Site, Durango, La Plata County, Colorado  

Broader source: Energy.gov [DOE]

The U.S. Department of Energy developed this statement to evaluate the environmental impacts of several scenarios for management and control of the residual radioactive wastes at the inactive Durango, Colorado, uranium processing site, including a no action alternative, an alternative to manage wastes on-site and three alternatives involving off-site management and decontamination of the Durango site.

235

Automated UF6 Cylinder Enrichment Assay: Status of the Hybrid Enrichment Verification Array (HEVA) Project: POTAS Phase II  

SciTech Connect (OSTI)

Pacific Northwest National Laboratory (PNNL) intends to automate the UF6 cylinder nondestructive assay (NDA) verification currently performed by the International Atomic Energy Agency (IAEA) at enrichment plants. PNNL is proposing the installation of a portal monitor at a key measurement point to positively identify each cylinder, measure its mass and enrichment, store the data along with operator inputs in a secure database, and maintain continuity of knowledge on measured cylinders until inspector arrival. This report summarizes the status of the research and development of an enrichment assay methodology supporting the cylinder verification concept. The enrichment assay approach exploits a hybrid of two passively-detected ionizing-radiation signatures: the traditional enrichment meter signature (186-keV photon peak area) and a non-traditional signature, manifested in the high-energy (3 to 8 MeV) gamma-ray continuum, generated by neutron emission from UF6. PNNL has designed, fabricated, and field-tested several prototype assay sensor packages in an effort to demonstrate proof-of-principle for the hybrid assay approach, quantify the expected assay precision for various categories of cylinder contents, and assess the potential for unsupervised deployment of the technology in a portal-monitor form factor. We refer to recent sensor-package prototypes as the Hybrid Enrichment Verification Array (HEVA). The report provides an overview of the assay signatures and summarizes the results of several HEVA field measurement campaigns on populations of Type 30B UF6 cylinders containing low-enriched uranium (LEU), natural uranium (NU), and depleted uranium (DU). Approaches to performance optimization of the assay technique via radiation transport modeling are briefly described, as are spectroscopic and data-analysis algorithms.

Jordan, David V.; Orton, Christopher R.; Mace, Emily K.; McDonald, Benjamin S.; Kulisek, Jonathan A.; Smith, Leon E.

2012-06-01T23:59:59.000Z

236

Method for electrochemical decontamination of radioactive metal  

DOE Patents [OSTI]

A decontamination method for stripping radionuclides from the surface of stainless steel or aluminum material comprising the steps of contacting the metal with a moderately acidic carbonate/bicarbonate electrolyte solution containing sodium or potassium ions and thereafter electrolytically removing the radionuclides from the surface of the metal whereby radionuclides are caused to be stripped off of the material without corrosion or etching of the material surface.

Ekechukwu, Amy A. (Augusta, GA)

2008-06-10T23:59:59.000Z

237

Reduced-Enrichment Research and Test Reactor Program: Environmental assessment  

SciTech Connect (OSTI)

The principal program objective and principal part of the proposed action is to improve the proliferation resistance of nuclear fuels used in research and test reactors by providing the technical means (through technical development, design, and testing) for reducing the uranium enrichment requirements of these fuels to substantially less than the 90 to 93% enrichment currently used. Operator acceptance of the reduced-enrichment-uranium (REU) fuel alternative will require minimizing of reactor performance reduction, fuel cycle cost increases, the number of new safety and licensing issues raised, and reactor and facility modifications. The other part of the proposed action is to assure the capability for commercial production and supply of REU fuel for use both in the US and abroad. The RERTR Program scope is limited to generic design studies, technical support to reactor operating organizations in preparing for conversions to REU fuels, fuel development, fuel demonstrations, and technical support for commercialization of REU fuels. This environmental assessment addresses the environmental consequences of RERTR Program activities and of specific conversions of typical reactors (the Ford Nuclear Reactor and one or two other to-be-designated demonstrations) to REU-fuel cycles, including domestic and international shipments of enriched uranium pertinent to the conduct of RERTR Program activities.

Not Available

1980-05-01T23:59:59.000Z

238

Equipment decontamination: A brief survey of the DOE complex  

SciTech Connect (OSTI)

Deactivation at DOE facilities has left a tremendous amount of contaminated equipment behind. In-situ methods are needed to decontaminate the interiors of the equipment sufficiently to allow either free release or land disposal. A brief survey was completed of the DOE complex on their needs for equipment decontamination with in-situ technology to determine (1) the types of contamination problems within the DOE complex, (2) decontamination processes that are being used or are being developed within the DOE, and (3) the methods that are available to dispose of spent decontamination solutions. In addition, potential sites for testing decontamination methods were located. Based on the information obtained from these surveys, the Rocky Flats Plant and the Idaho National Engineering Laboratory appear to be best suited to complete the initial testing of the decontamination processes.

Conner, C.; Chamberlain, D.B; Chen, L.; Vandegrift, G.F.

1995-03-01T23:59:59.000Z

239

Development of decontamination techniques for decommissioning commercial nuclear power plants  

SciTech Connect (OSTI)

NUPEC has been developing various techniques to safely and efficiently decommission large commercial nuclear power plants. The development work, referred to as the verification tests, has been performed since 1982. The verification tests on decontamination techniques have focused on the reduction of both occupational radiation exposure and radioactive waste volume. Experiments on various decontamination methods have been carried out. Prospects of applying efficient decontamination techniques to commercial nuclear power plant decommissioning are bright due to the experimental results.

Ishikura, T.; Miwa, T.; Onozawa, T.; Ohtsuka, H. [Nuclear Power Engineering Corp., Tokyo (Japan). Plant and Components Dept.; Ishigure, K. [Univ. of Tokyo (Japan). Dept. of Quantum Engineering and System Science

1993-12-31T23:59:59.000Z

240

Corrective Action Decision Document for Corrective Action Unit 254: Area 25 R-MAD Decontamination Facility, Nevada Test Site, Nevada  

SciTech Connect (OSTI)

This Corrective Action Decision Document identifies and rationalizes the US Department of Energy, Nevada Operations Office's selection of a recommended corrective action alternative (CAA) appropriate to facilitate the closure of Corrective Action Unit (CAU) 254, R-MAD Decontamination Facility, under the Federal Facility Agreement and Consent Order. Located in Area 25 at the Nevada Test Site in Nevada, CAU 254 is comprised of Corrective Action Site (CAS) 25-23-06, Decontamination Facility. A corrective action investigation for this CAS as conducted in January 2000 as set forth in the related Corrective Action Investigation Plan. Samples were collected from various media throughout the CAS and sent to an off-site laboratory for analysis. The laboratory results indicated the following: radiation dose rates inside the Decontamination Facility, Building 3126, and in the storage yard exceeded the average general dose rate; scanning and static total surface contamination surveys indicated that portions of the locker and shower room floor, decontamination bay floor, loft floor, east and west decon pads, north and south decontamination bay interior walls, exterior west and south walls, and loft walls were above preliminary action levels (PALs). The investigation-derived contaminants of concern (COCs) included: polychlorinated biphenyls, radionuclides (strontium-90, niobium-94, cesium-137, uranium-234 and -235), total volatile and semivolatile organic compounds, total petroleum hydrocarbons, and total Resource Conservation and Recovery Act (Metals). During the investigation, two corrective action objectives (CAOs) were identified to prevent or mitigate human exposure to COCs. Based on these CAOs, a review of existing data, future use, and current operations at the Nevada Test Site, three CAAs were developed for consideration: Alternative 1 - No Further Action; Alternative 2 - Unrestricted Release Decontamination and Verification Survey; and Alternative 3 - Unrestricted Release Decontamination and Verification Survey and Dismantling of Building 3126. These alternatives were evaluated based on four general corrective action standards and five remedy selection decision factors, and the preferred CAA chosen on technical merit was Alternative 2. This CAA was judged to meet all requirements for the technical components evaluated and applicable state and federal regulations for closure of the site, and reduce the potential for future exposure pathways.

U.S. Department of Energy, Nevada Operations Office

2000-06-01T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


241

Selective leaching of uranium from uranium-contaminated soils: Progress report 1  

SciTech Connect (OSTI)

Three soils and a sediment contaminated with uranium were used to determine the effectiveness of sodium carbonate and citric acid leaching to decontaminated or remove uranium to acceptable regulatory levels. Two of the soils were surface soils from the DOE facility formerly called the Feed Materials Production Center (FMPC) at Fernald, Ohio. This facility is presently called the Femald Environmental Management Project (FEMP). Carbonate extractions generally removed from 70 to 90% of the uranium from the Fernald storage pad soil. Uranium was slightly more difficult to extract from the Fernald incinerator and the Y-12 landfarm soils. Very small amounts of uranium could be extracted from the storm sewer sediment. Extraction with carbonate at high solution-to-soil ratios were as effective as extractions at low solution-to-soil ratios, indicating attrition by the paddle mixer was not significantly different than that provided in a rotary extractor. Also, pretreatments such as milling or pulverizing the soil sample did not appear to increase extraction efficiency when carbonate extractions were carried out at elevated temperatures (60[degree]C) or long extraction times (23 h). Adding KMnO[sub 4] in the carbonate extraction appeared to increase extraction efficiency from the Fernald incinerator soil but not the Fernald storage pad soil. The most effective leaching rates (> 90 % from both Fernald soils) were obtained using a citrate/dithionite extraction procedure designed to remove amorphous (noncrystalline) iron/aluminum sesquioxides from surfaces of clay minerals. Citric acid also proved to be a very good extractant for uranium.

Francis, C.W.; Mattus, A.J.; Farr, L.L.; Elless, M.P.; Lee, S.Y.

1993-02-01T23:59:59.000Z

242

Selective leaching of uranium from uranium-contaminated soils: Progress report 1  

SciTech Connect (OSTI)

Three soils and a sediment contaminated with uranium were used to determine the effectiveness of sodium carbonate and citric acid leaching to decontaminated or remove uranium to acceptable regulatory levels. Two of the soils were surface soils from the DOE facility formerly called the Feed Materials Production Center (FMPC) at Fernald, Ohio. This facility is presently called the Femald Environmental Management Project (FEMP). Carbonate extractions generally removed from 70 to 90% of the uranium from the Fernald storage pad soil. Uranium was slightly more difficult to extract from the Fernald incinerator and the Y-12 landfarm soils. Very small amounts of uranium could be extracted from the storm sewer sediment. Extraction with carbonate at high solution-to-soil ratios were as effective as extractions at low solution-to-soil ratios, indicating attrition by the paddle mixer was not significantly different than that provided in a rotary extractor. Also, pretreatments such as milling or pulverizing the soil sample did not appear to increase extraction efficiency when carbonate extractions were carried out at elevated temperatures (60{degree}C) or long extraction times (23 h). Adding KMnO{sub 4} in the carbonate extraction appeared to increase extraction efficiency from the Fernald incinerator soil but not the Fernald storage pad soil. The most effective leaching rates (> 90 % from both Fernald soils) were obtained using a citrate/dithionite extraction procedure designed to remove amorphous (noncrystalline) iron/aluminum sesquioxides from surfaces of clay minerals. Citric acid also proved to be a very good extractant for uranium.

Francis, C.W.; Mattus, A.J.; Farr, L.L.; Elless, M.P.; Lee, S.Y.

1993-02-01T23:59:59.000Z

243

Reports on investigations of uranium anomalies. National Uranium Resource Evaluation  

SciTech Connect (OSTI)

During the National Uranium Resource Evaluation (NURE) program, conducted for the US Department of Energy (DOE) by Bendix Field Engineering Corporation (BFEC), radiometric and geochemical surveys and geologic investigations detected anomalies indicative of possible uranium enrichment. Data from the Aerial Radiometric and Magnetic Survey (ARMS) and the Hydrogeochemical and Stream-Sediment Reconnaissance (HSSR), both of which were conducted on a national scale, yielded numerous anomalies that may signal areas favorable for the occurrence of uranium deposits. Results from geologic evaluations of individual 1/sup 0/ x 2/sup 0/ quadrangles for the NURE program also yielded anomalies, which could not be adequately checked during scheduled field work. Included in this volume are individual reports of field investigations for the following six areas which were shown on the basis of ARMS, HSSR, and (or) geologic data to be anomalous: (1) Hylas zone and northern Richmond basin, Virginia; (2) Sischu Creek area, Alaska; (3) Goodman-Dunbar area, Wisconsin; (4) McCaslin syncline, Wisconsin; (5) Mt. Withington Cauldron, Socorro County, New Mexico; (6) Lake Tecopa, Inyo County, California. Field checks were conducted in each case to verify an indicated anomalous condition and to determine the nature of materials causing the anomaly. The ultimate objective of work is to determine whether favorable conditions exist for the occurrence of uranium deposits in areas that either had not been previously evaluated or were evaluated before data from recent surveys were available. Most field checks were of short duration (2 to 5 days). The work was done by various investigators using different procedures, which accounts for variations in format in their reports. All papers have been abstracted and indexed.

Goodknight, C.S.; Burger, J.A. (comps.) [comps.

1982-10-01T23:59:59.000Z

244

Final Environmental Impact Statement for the construction and operation of Claiborne Enrichment Center, Homer, Louisiana (Docket No. 70-3-70). Volume 2, Public comments and NRC response  

SciTech Connect (OSTI)

The Final Environmental Impact Statement (FEIS) (Volume 1), was prepared by the Nuclear Regulatory Commission (NRC) in accordance with regulation 10 CFR Part 51, which implements the National Environmental Policy Act (NEPA), to assess the potential environmental impacts for licensing the construction and operation of a proposed gaseous centrifuge enrichment facility to be built in Claiborne Parish, Louisiana by Louisiana Energy Services, L.P. (LES). The proposed facility would have a production capacity of about 866 metric tons annually of up to 5 weight percent enriched UF{sub 6}, using a proven centrifuge technology. Included in the assessment are co on, both normal operations and potential accidents (internal and external events), and the eventual decontamination and decommissioning of the site. In order to help assure that releases from the operation of the facility and potential impacts on the public are as low as reasonably achievable, an environmental monitoring program was developed by LES to detect significant changes in the background levels of uranium around the site. Other issues addressed include the purpose and need for the facility, the alternatives to the proposed action, potential disposition of the tails, the site selection process, and environmental justice. The NRC staff concludes that the facility can be constructed and operated with small and acceptable impacts on the public and the environment, and proposes to issue a license to the applicant, Louisiana Energy Services, to authorize construction and operation of the proposed facility. The letters in this Appendix have been divided into three sections. Section One contains letters to which the NRC responded by addressing specific comments. Section Two contains the letters that concerned the communities of Forest Grove and Center Springs. Section Three is composed of letters that required no response. These letters were generally in support of the facility.

Zeitoun, A. [Science Applications International Corp., Germantown, MD (United States)

1994-08-01T23:59:59.000Z

245

The study of material accountancy procedures for uranium in a whole nuclear fuel cycle  

SciTech Connect (OSTI)

Material accountancy procedures for uranium under a whole nuclear fuel cycle were studied by taking into consideration the material accountancy capability associated with realistic measurement uncertainties. The significant quantity used by the International Atomic Energy Agency (IAEA) for low-enriched uranium is 75 kg U-235 contained. A loss of U-235 contained in uranium can be detected by either of the following two procedures: one is a traditional U-235 isotope balance, and the other is a total uranium element balance. Facility types studied in this paper were UF6 conversion, gas centrifuge uranium enrichment, fuel fabrication, reprocessing, plutonium conversion, and MOX fuel production in Japan, where recycled uranium is processed in addition to natural uranium. It was found that the material accountancy capability of a total uranium element balance was almost always higher than that of a U-235 isotope balance under normal accuracy of weight, concentration, and enrichment measurements. Changing from the traditional U-235 isotope balance to the total uranium element balance for these facilities would lead to a gain of U-235 loss detection capability through material accountancy and to a reduction in the required resources of both the IAEA and operators.

Nakano, Hiromasa; Akiba, Mitsunori [Power Reactor and Nuclear Fuel Development Corp., Tokyo (Japan)

1995-07-01T23:59:59.000Z

246

Derivation of uranium residual radioactive material guidelines for the Shpack site  

SciTech Connect (OSTI)

Residual radioactive material guidelines for uranium were derived for the Shpack site in Norton, Massachusetts. This site has been identified for remedial action under the Formerly Utilized Sites Remedial Action Program (FUSRAP) of the US Department of Energy (DOE). The uranium guidelines were derived on the basis of the requirement that the 50-year committed effective dose equivalent to a hypothetical individual who lives or works in the immediate vicinity of the Shpack site should not exceed a dose of 100 mrem/yr following decontamination. The DOE residual radioactive material guideline computer code, RESRAD, which implements the methodology described in the DOE manual for implementing residual radioactive material guidelines, was used in this evaluation. Three potential scenarios were considered for the site; the scenarios vary with regard to time spent at the site, sources of water used, and sources of food consumed. The results of the evaluation indicate that the basic dose limit of 100 mrem/yr will not be exceeded for uranium (including uranium-234, uranium-235, and uranium-238) within 1000 years, provided that the soil concentration of combined uranium (uranium-234 and uranium-238) at the Shpack site does not exceed the following levels: 2500 pCi/g for Scenario A (recreationist: the expected scenario); 1100 pCi/g for Scenario B (industrial worker: a plausible scenario); and 53 pCi/g for Scenario C (resident farmer using a well water as the only water source: a possible but unlikely scenario). The uranium guidelines derived in this report apply to the combined activity concentration of uranium-234 and uranium-238 and were calculated on the basis of a dose of 100 mrem/yr. In setting the actual uranium guidelines for the Shpack site, DOE will apply the as low as reasonably achievable (ALARA) policy to the decision-making process, along with other factors, such as whether a particular scenario is reasonable and appropriate. 8 refs., 2 figs., 8 tabs.

Cheng, J.J.; Yu, C.; Monette, F.; Jones, L.

1991-08-01T23:59:59.000Z

247

EIS-0471: Department of Energy Loan Guarantee to Support Proposed Eagle Rock Enrichment Facility in Bonneville County, Idaho  

Broader source: Energy.gov [DOE]

This EIS evaluates the environmental impacts of construction, operation, and decommissioning of the proposed Eagle Rock Enrichment Facility (EREF), a gas centrifuge uranium enrichment facility to be located in a rural area in western Bonneville County, Idaho. (DOE adopted this EIS issued by NRC on 04/13/2007.)

248

DECONTAMINATION FACTORS AND FILTRATION FLUX IMPACT TO ARP AT REDUCED MST CONCENTRATION  

SciTech Connect (OSTI)

Tank Farm and Closure Engineering is evaluating changes to the Actinide Removal Process facility operations to decrease the MST concentration from 0.4 g/L to 0.2 g/L and the contact time from 12 hours to between 6 and 8 hours. For this evaluation, SRNL reviewed previous datasets investigating the performance of MST at 0.2 g/L in salt solutions ranging from 4.5 to 7.5 M in sodium concentration. In general, reducing the MST concentration from 0.4 to 0.2 g/L and increasing the ionic strength from 4.5 to 7.5 M in sodium concentration will decrease the measured decontamination factors for plutonium, neptunium, uranium and strontium. The decontamination factors as well as single standard deviation values for each sorbate are reported. These values are applicable within the sorbate and sodium concentrations used in the experimental measurements. Decreasing the MST concentration in the ARP from 0.4 g/L to 0.2 g/L will produce an increase in the filter flux, and could lead to longer operating times between filter cleaning. The increase in flux is a function of a number of operating parameters, and is difficult to quantify. However, it is estimated that the reduction in MST could result in a reduction of filtration time of up to 20%.

Hobbs, D.

2012-06-27T23:59:59.000Z

249

Technical Report: Contaminant Organic Complexes: Their structure and energetics in surface decontamination  

SciTech Connect (OSTI)

The Department of Energy has a goal of decontaminating an estimated 180,000 metric tons of metal wastes in various surplus facilities. Uranium (U) and other radioactive actinides and lanthanides are embedded within the mixed oxide structures of the passivity layers of corroded iron and steel. These toxic metals can be dissolved out of the surface layers by a naturally occurring bacterial siderophore called Desferrioxamine B (DFB). DFB is a trihydroxamate ligand with one amine (pK1 =10.89) and three hydroxamate groups (pK2 =9.70, pK3 =9.03, and pK4 =8.30), which chelates with metals through hydroxamate coordination. Complexation of DFB with U can be utilized in decontamination strategy of the passivity layers. Therefore, we have been studying reactions of uranyl U(VI) with zerovalent iron (Fe0) followed by dissolution by DFB. The objectives were to determine the structure and speciation of solution and solid phases of U and to assess the effectiveness of DFB in U dissolution.

Samuel J. Traina; Shankar Sharma

2007-04-22T23:59:59.000Z

250

Decontamination, decommissioning, and vendor advertorial issue, 2005  

SciTech Connect (OSTI)

The focus of the July-August issue is on Decontamination, decommissioning, and vendor advertorials. Major interviews, articles and reports in this issue include: Increasing momentum, by Gary Taylor, Entergy Nuclear, Inc.; An acceptable investment, by Tom Chrisopher, Areva, Inc.; Fuel recycling for the U.S. and abroad, by Philippe Knoche, Areva, France; We're bullish on nuclear power, by Dan R. Keuter, Entergy Nuclear, Inc.; Ten key actions for decommissioning, by Lawrence E. Boing, Argonne National Laboratory; Safe, efficient and cost-effective decommissioning, by Dr. Claudio Pescatore and Torsten Eng, OECD Nuclear Energy Agency (NEA), France; and, Plant profile: SONGS decommissioning.

Agnihotri, Newal (ed.)

2005-07-15T23:59:59.000Z

251

SEDIMENT DECONTAMINATION TREATMENT TRAIN: COMMERCIAL-SCALE DEMONSTRATION  

E-Print Network [OSTI]

1 SEDIMENT DECONTAMINATION TREATMENT TRAIN: COMMERCIAL-SCALE DEMONSTRATION FOR THE PORT OF NEW YORK York and New Jersey. We describe here a regional contaminated sediment decontamination program) public outreach. Several types of treatment technologies suitable for use with varying levels of sediment

Brookhaven National Laboratory

252

Enrichment Assay Methods for a UF6 Cylinder Verification Station  

SciTech Connect (OSTI)

International Atomic Energy Agency (IAEA) inspectors currently perform periodic inspections at uranium enrichment plants to verify UF6 cylinder enrichment declarations. Measurements are typically performed with handheld high-resolution sensors on a sampling of cylinders taken to be representative of the facility’s entire cylinder inventory. These enrichment assay methods interrogate only a small fraction of the total cylinder volume, and are time-consuming and expensive to execute for inspectors. Pacific Northwest National Laboratory (PNNL) is developing an unattended measurement system capable of automated enrichment measurements over the full volume of Type 30B and Type 48 cylinders. This Integrated Cylinder Verification System (ICVS) could be located at key measurement points to positively identify each cylinder, measure its mass and enrichment, store the collected data in a secure database, and maintain continuity of knowledge on measured cylinders until IAEA inspector arrival. The focus of this paper is the development of nondestructive assay (NDA) methods that combine “traditional” enrichment signatures (e.g. 185-keV emission from U-235) and more-penetrating “non-traditional” signatures (e.g. high-energy neutron-induced gamma rays spawned primarily from U-234 alpha emission) collected by medium-resolution gamma-ray spectrometers (i.e. sodium iodide or lanthanum bromide). The potential of these NDA methods for the automated assay of feed, tail and product cylinders is explored through MCNP modeling and with field measurements on a cylinder population ranging from 0.2% to 5% in U-235 enrichment.

Smith, Leon E.; Jordan, David V.; Misner, Alex C.; Mace, Emily K.; Orton, Christopher R.

2010-11-30T23:59:59.000Z

253

The Office of Environmental Management Uranium Enrichment D&D...  

Energy Savers [EERE]

and Staffing Plan Report - Portsmouth Paducah Project Office Above on the left is K-25, at Oak Ridge before and after the 844,000 sq-ft demolition. In addition, on the...

254

Oak Ridge, Tenn. Selected as Uranium Enrichment Site | National Nuclear  

National Nuclear Security Administration (NNSA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) "ofEarlyEnergyDepartment ofDepartment ofofOxford SiteToledoSampling at theOfficials to discuss NPT

255

Highly Enriched Uranium Materials Facility | Y-12 National Security Complex  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-SeriesFlickr FlickrGuidedCH2MLLC High-Rate,Highlights Highlights Below is aHighly

256

Highly Enriched Uranium Transparency Program | National Nuclear Security  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-SeriesFlickr FlickrGuidedCH2MLLC High-Rate,Highlights Highlights Below is

257

Highly Enriched Uranium Materials Facility, Major Design Changes  

Office of Environmental Management (EM)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelinesProvedDecember 2005DepartmentDecemberGlossaryEnergy and Commerceof Energy

258

US, Kazakhstan Cooperate to Eliminate Highly Enriched Uranium | National  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsrucLasDelivered energy consumption by sectorlong version) The0 -ITER's centralNewUSUS

259

NNSA helps eliminate highly enriched uranium from Kazakhstan...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Kazakhstan. The HEU was transported via two air shipments to a secure facility in Russia for permanent disposition. This complex operation was the culmination of a multi-year...

260

Italy Highly Enriched Uranium and Plutonium Removals | National Nuclear  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-SeriesFlickrinformation for andFuel-Efficient Engines |Iron isCancerFuelIt

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
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they are not comprehensive nor are they the most current set.
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261

Special Nuclear Materials: EM Manages Plutonium, Highly Enriched Uranium  

Broader source: Energy.gov (indexed) [DOE]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) "ofEarly Career Scientists' Research |RegulationRenewable EnergySouthwest MichiganNovember 27, 2006November

262

Belgium Highly Enriched Uranium and Plutonium Removals | National Nuclear  

National Nuclear Security Administration (NNSA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) "ofEarlyEnergyDepartment ofDepartment ofofOxford SiteToledoSampling atSFO |Alternate| National

263

NNSA and Kazakhstan Complete Operation to Eliminate Highly Enriched Uranium  

National Nuclear Security Administration (NNSA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) "ofEarlyEnergyDepartment ofDepartment ofofOxfordVeterans |NuclearOffice of GeneralLaboratory |Nuclear|

264

GTRI's Convert Program: Minimizing the Use of Highly Enriched Uranium |  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-SeriesFlickr Flickr Editor's note:ComputingFusionSanGE Global40-DOPGTC

265

German Pebble Bed Research Reactor Highly Enriched Uranium (HEU) Fuel  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-SeriesFlickr Flickr Editor'sshortGeothermal Heat PumpsChad Simmons Gerdenis Kodis

266

Toxic Substances Control Act Uranium Enrichment Federal Facility Compliance  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious Rank EERE:YearRound-Up from theDepartment of EnergyThe Sun and ItsXVIIofPotential

267

Active Waste Materials Corrosion and Decontamination Tests  

SciTech Connect (OSTI)

Stainless steel alloys, 304L and 316L, were corrosion tested in representative radioactive samples of three actual Hanford tank waste solutions (Tanks AW-101, C-104, AN-107). Both the 304L and 316L exhibited good corrosion performance when immersed in boiling waste solutions. The maximum general corrosion rate was 0.015 mm/y (0.60 mils per year). Generally, the 304L had a slightly higher rate than the 316L. No localized attack was observed after 122 days of testing in the liquid phase, liquid/vapor phase, or vapor phase. Radioactive plate-out decontamination tests indicated that a 24-hour exposure to 1 {und M} HNO{sub 3} could remove about 99% of the radioactive components in the metal film when exposed to the C-104 and AN-107 solutions. The decontamination results are less certain for the AW-101 solution, since the initial contamination readings exceeded the capacity of the meter used for this test.

MJ Danielson; MR Elmore; SG Pitman

2000-08-15T23:59:59.000Z

268

Criticality safety concerns of uranium deposits in cascade equipment  

SciTech Connect (OSTI)

The Paducah and Portsmouth Gaseous Diffusion Plants enrich uranium in the {sup 235}U isotope by diffusing gaseous uranium hexafluoride (UF{sub 6}) through a porous barrier. The UF{sub 6} gaseous diffusion cascade utilized several thousand {open_quotes}stages{close_quotes} of barrier to produce highly enriched uranium (HEU). Historically, Portsmouth has enriched the Paducah Gaseous Diffusion Plant`s product (typically 1.8 wt% {sup 235}U) as well as natural enrichment feed stock up to 97 wt%. Due to the chemical reactivity of UF{sub 6}, particularly with water, the formation of solid uranium deposits occur at a gaseous diffusion plant. Much of the equipment operates below atmospheric pressure, and deposits are formed when atmospheric air enters the cascade. Deposits may also be formed from UF{sub 6} reactions with oil, UF{sub 6} reactions with the metallic surfaces of equipment, and desublimation of UF{sub 6}. The major deposits form as a result of moist air in leakage due to failure of compressor casing flanges, blow-off plates, seals, expansion joint convolutions, and instrument lines. This report describes criticality concerns and deposit disposition.

Plaster, M.J. [Lockheed Martin Utility Services, Inc., Piketon, OH (United States)

1996-12-31T23:59:59.000Z

269

In-line assay monitor for uranium hexafluoride  

DOE Patents [OSTI]

An in-line assay monitor for determining the content of uranium-235 in a uranium hexafluoride gas isotopic separation system is provided which removes the necessity of complete access to the operating parameters of the system for determining the uranium-235 content. The monitor is intended for uses such as safeguard applications to assure that weapons grade uranium is not being produced in an enrichment cascade. The method and monitor for carrying out the method involve cooling of a radiation pervious chamber connected in fluid communication with the selected point in the system to withdraw a specimen and solidify the specimen in the chamber. The specimen is irradiated by means of an ionizing radiation source of energy different from that of the 185 keV gamma emissions from the uranium-235 present in the specimen. Simultaneously, the gamma emissions from the uranium-235 of the specimen and the source emissions transmitted through the sample are counted and stored in a multiple channel analyzer. The uranium-235 content of the specimen is determined from the comparison of the accumulated 185 keV energy counts and the reference energy counts. The latter is used to measure the total uranium isotopic content of the specimen. The process eliminates the necessity of knowing the system operating conditions and yet obtains the necessary data without need for large scintillation crystals and sophisticated mechanical designs.

Wallace, Steven A. (Knoxville, TN)

1981-01-01T23:59:59.000Z

270

Final Uranium Leasing Program Programmatic Environmental Impact...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Final Uranium Leasing Program Programmatic Environmental Impact Statement (PEIS) Final Uranium Leasing Program Programmatic Environmental Impact Statement (PEIS) Uranium Leasing...

271

Final report of the decontamination and decommissioning of the exterior land areas at the Grand Junction Projects Office facility  

SciTech Connect (OSTI)

The US Department of Energy (DOE) Grand Junction Projects Office (GJPO) facility occupies approximately 56.4 acres (22.8 hectares) along the Gunnison River near Grand Junction, Colorado. The site was contaminated with uranium ore and mill tailings during uranium-refining activities conducted by the Manhattan Engineer District and during pilot-milling experiments conducted for the US Atomic Energy Commission`s (AEC`s) domestic uranium procurement program. The GJPO facility was the collection and assay point for AEC uranium and vanadium oxide purchases until the early 1970s. The DOE Decontamination and Decommissioning Program sponsored the Grand Junction Projects Office Remedial Action Project (GJPORAP) to remediate the facility lands, site improvements, and the underlying aquifer. The site contractor, Rust Geotech, was the Remedial Action Contractor for GJPORAP. The exterior land areas of the facility assessed as contaminated have been remediated in accordance with identified standards and can be released for unrestricted use. Restoration of the aquifer will be accomplished through the natural flushing action of the aquifer during the next 50 to 80 years. The remediation of the DOE-GJPO facility buildings is ongoing and will be described in a separate report.

Widdop, M.R.

1995-09-01T23:59:59.000Z

272

Depleted Uranium Technical Brief  

E-Print Network [OSTI]

Depleted Uranium Technical Brief United States Environmental Protection Agency Office of Air and Radiation Washington, DC 20460 EPA-402-R-06-011 December 2006 #12;#12;Depleted Uranium Technical Brief EPA of Radiation and Indoor Air Radiation Protection Division ii #12;iii #12;FOREWARD The Depleted Uranium

273

Preliminary study on weapon grade uranium utilization in molten salt reactor miniFUJI  

SciTech Connect (OSTI)

Preliminary study on weapon grade uranium utilization in 25MWth and 50MWth of miniFUJI MSR (molten salt reactor) has been carried out. In this study, a very high enriched uranium that we called weapon grade uranium has been employed in UF{sub 4} composition. The {sup 235}U enrichment is 90 - 95 %. The results show that the 25MWth miniFUJI MSR can get its criticality condition for 1.56 %, 1.76%, and 1.96% of UF{sub 4} with {sup 235}U enrichment of at least 93%, 90%, and 90%, respectively. In contrast, the 50 MWth miniFUJI reactor can be critical for 1.96% of UF{sub 4} with {sup 235}U enrichment of at smallest amount 95%. The neutron spectra are almost similar for each power output.

Aji, Indarta Kuncoro [Department of Physics, Faculty of Mathematics and Natural Sciences, Institut Teknologi Bandung (Indonesia); Waris, A., E-mail: awaris@fi.itb.ac.id [Nuclear Physics and Biophysics Research Division, Department of Physics, Faculty of Mathematics and Natural Sciences, Institut Teknologi Bandung, Jl. Ganesa No. 10 Bandung 40132 (Indonesia)

2014-09-30T23:59:59.000Z

274

Detection of illicit HEU production in gaseous centrifuge enrichment plants using neutron counting techniques on product cylinders  

SciTech Connect (OSTI)

Innovative and novel safeguards approaches are needed for nuclear energy to meet global energy needs without the threat of nuclear weapons proliferation. Part of these efforts will include creating verification techniques that can monitor uranium enrichment facilities for illicit production of highly-enriched uranium (HEU). Passive nondestructive assay (NDA) techniques will be critical in preventing illicit HEU production because NDA offers the possibility of continuous and unattended monitoring capabilities with limited impact on facility operations. Gaseous centrifuge enrichment plants (GCEP) are commonly used to produce low-enriched uranium (LEU) for reactor fuel. In a GCEP, gaseous UF{sub 6} spins at high velocities in centrifuges to separate the molecules containing {sup 238}U from those containing the lighter {sup 235}U. Unfortunately, the process for creating LEU is inherently the same as HEU, creating a proliferation concern. Insuring that GCEPs are producing declared enrichments poses many difficult challenges. In a GCEP, large cascade halls operating thousands of centrifuges work together to enrich the uranium which makes effective monitoring of the cascade hall economically prohibitive and invasive to plant operations. However, the enriched uranium exiting the cascade hall fills product cylinders where the UF{sub 6} gas sublimes and condenses for easier storage and transportation. These product cylinders hold large quantities of enriched uranium, offering a strong signal for NDA measurement. Neutrons have a large penetrability through materials making their use advantageous compared to gamma techniques where the signal is easily attenuated. One proposed technique for detecting HEU production in a GCEP is using neutron coincidence counting at the product cylinder take off stations. This paper discusses findings from Monte Carlo N-Particle eXtended (MCNPX) code simulations that examine the feasibility of such a detector.

Freeman, Corey R [Los Alamos National Laboratory; Geist, William H [Los Alamos National Laboratory

2010-01-01T23:59:59.000Z

275

Decontamination Systems Information and Research Program. Quarterly technical progress report, January 1--March 31, 1994  

SciTech Connect (OSTI)

West Virginia University (WVU) and the US DOE Morgantown Energy Technology Center (METC) entered into a Cooperative Agreement on August 29, 1992 entitled ``Decontamination Systems Information and Research Programs.`` Stipulated within the Agreement is the requirement that WVU submit to METC a series of Technical Progress Reports on a quarterly basis. This report comprises the first Quarterly Technical Progress Report for Year 2 of the Agreement. This report reflects the progress and/or efforts performed on the sixteen (16) technical projects encompassed by the Year 2 Agreement for the period of January 1 through March 31, 1994. In situ bioremediation of chlorinated organic solvents; Microbial enrichment for enhancing in-situ biodegradation of hazardous organic wastes; Treatment of volatile organic compounds (VOCs) using biofilters; Drain-enhanced soil flushing (DESF) for organic contaminants removal; Chemical destruction of chlorinated organic compounds; Remediation of hazardous sites with steam reforming; Soil decontamination with a packed flotation column; Use of granular activated carbon columns for the simultaneous removal of organics, heavy metals, and radionuclides; Monolayer and multilayer self-assembled polyion films for gas-phase chemical sensors; Compact mercuric iodide detector technology development; Evaluation of IR and mass spectrometric techniques for on-site monitoring of volatile organic compounds; A systematic database of the state of hazardous waste clean-up technologies; Dust control methods for insitu nuclear and hazardous waste handling; Winfield Lock and Dam remediation; and Socio-economic assessment of alternative environmental restoration technologies.

Not Available

1994-05-01T23:59:59.000Z

276

Long-term decontamination engineering study. Volume 1  

SciTech Connect (OSTI)

This report was prepared by Westinghouse Hanford Company (WHC) with technical and cost estimating support from Pacific Northwest Laboratories (PNL) and Parsons Environmental Services, Inc. (Parsons). This engineering study evaluates the requirements and alternatives for decontamination/treatment of contaminated equipment at the Hanford Site. The purpose of this study is to determine the decontamination/treatment strategy that best supports the Hanford Site environmental restoration mission. It describes the potential waste streams requiring treatment or decontamination, develops the alternatives under consideration establishes the criteria for comparison, evaluates the alternatives, and draws conclusions (i.e., the optimum strategy for decontamination). Although two primary alternatives are discussed, this study does identify other alternatives that may warrant additional study. hanford Site solid waste management program activities include storage, special processing, decontamination/treatment, and disposal facilities. This study focuses on the decontamination/treatment processes (e.g., waste decontamination, size reduction, immobilization, and packaging) that support the environmental restoration mission at the Hanford Site.

Geuther, W.J.

1995-04-03T23:59:59.000Z

277

Corrosion Evaluation of RERTR Uranium Molybdenum Fuel  

SciTech Connect (OSTI)

As part of the National Nuclear Security Agency (NNSA) mandate to replace the use of highly enriched uranium (HEU) fuel for low enriched uranium (LEU) fuel, research into the development of LEU fuel for research reactors has been active since the late 1970’s. Originally referred to as the Reduced Enrichment for Research and Test Reactor (RERTR) program the new effort named Global Threat Reduction Initiative (GTRI) is nearing the goal of replacing the standard aluminum clad dispersion highly enriched uranium aluminide fuel with a new LEU fuel. The five domestic high performance research reactors undergoing this conversion are High Flux Isotope reactor (HFIR), Advanced Test Reactor (ATR), National Institute of Standards and Technology (NIST) Reactor, Missouri University Research Reactor (MURR) and the Massachusetts Institute of Technology Reactor II (MITR-II). The design of these reactors requires a higher neutron flux than other international research reactors, which to this point has posed unique challenges in the design and development of the new mandated LEU fuel. The new design utilizes a monolithic fuel configuration in order to obtain sufficient 235U within the LEU stoichoimetry to maintain the fission reaction within the domestic test reactors. The change from uranium aluminide dispersion fuel type to uranium molybdenum (UMo) monolithic configuration requires examination of possible corrosion issues associated with the new fuel meat. A focused analysis of the UMo fuel under potential corrosion conditions, within the ATR and under aqueous storage indicates a slow and predictable corrosion rate. Additional corrosion testing is recommended for the highest burn-up fuels to confirm observed corrosion rate trends. This corrosion analysis will focus only on the UMo fuel and will address corrosion of ancillary components such as cladding only in terms of how it affects the fuel. The calculations and corrosion scenarios are weighted with a conservative bias to provide additional confidence with the results. The actual corrosion rates of UMo fuel is very likely to be lower than assumed within this report which can be confirmed with additional testing.

A K Wertsching

2012-09-01T23:59:59.000Z

278

Health physics and industrial hygiene aspects of decontamination as a precursor to decontamination  

SciTech Connect (OSTI)

The Pacific Northwest Laboratory is conducting a comprehensive study of the impacts, benefits and effects of decontamination as a precursor to decommissioning for the US Nuclear Regulatory Commission. The program deals primarily with chemical cleaning of light-water reactor (LWR) systems that will not be returned to operation. A major section of this study defines the health physics and industrial hygiene and safety concerns during decontamination operations. The primary health physics concerns include providing adequate protection for workers from radiation sources which are transported by the decontamination processes, estimating and limiting radioactive effluents to the environment and maintaining operations in accordance with the ALARA philosophy. Locating and identifying the areas of contamination and measuring the radiation exposure rates throughout the reactor primary system are fundamental to implementing these health physics goals. The principal industrial hygiene and safety concerns stem from the fact that a nuclear power plant is being converted for a time to a chemical plant which will contain large volumes of chemical solutions.

Card, C.J.; Hoenes, G.R.; Munson, L.F.; Halseth, G.A.

1982-06-01T23:59:59.000Z

279

Method for converting uranium oxides to uranium metal  

DOE Patents [OSTI]

A process is described for converting scrap and waste uranium oxide to uranium metal. The uranium oxide is sequentially reduced with a suitable reducing agent to a mixture of uranium metal and oxide products. The uranium metal is then converted to uranium hydride and the uranium hydride-containing mixture is then cooled to a temperature less than -100.degree. C. in an inert liquid which renders the uranium hydride ferromagnetic. The uranium hydride is then magnetically separated from the cooled mixture. The separated uranium hydride is readily converted to uranium metal by heating in an inert atmosphere. This process is environmentally acceptable and eliminates the use of hydrogen fluoride as well as the explosive conditions encountered in the previously employed bomb-reduction processes utilized for converting uranium oxides to uranium metal.

Duerksen, Walter K. (Norris, TN)

1988-01-01T23:59:59.000Z

280

Decontamination Technologies, Task 3, Urban Remediation and Response Project  

SciTech Connect (OSTI)

In the aftermath of a Radiological Dispersal Device (RDD, also known as a dirty bomb) it will be necessary to remediate the site including building exteriors and interiors, equipment, pavement, vehicles, personal items etc. Remediation will remove or reduce radioactive contamination from the area using a combination of removing and disposing of many assets (including possible demolition of buildings), decontaminating and returning to service other assets, and fixing in place or leaving in place contamination that is deemed 'acceptable'. The later will require setting acceptable dose standards, which will require negotiation with all involved parties and a balance of risk and cost to benefit. To accomplish the first two, disposal or decontamination, a combination of technologies will be deployed that can be loosely classified as: Decontamination; Equipment removal and size reduction; and Demolition. This report will deal only with the decontamination technologies that will be used to return assets to service or to reduce waste disposal. It will not discuss demolition, size reduction or removal technologies or equipment (e.g., backhoe mounted rams, rock splitter, paving breakers and chipping hammers, etc.). As defined by the DOE (1994), decontamination is removal of radiological contamination from the surfaces of facilities and equipment. Expertise in this field comes primarily from the operation and decommissioning of DOE and commercial nuclear facilities as well as a small amount of ongoing research and development closely related to RDD decontamination. Information related to decontamination of fields, buildings, and public spaces resulting from the Goiania and Chernobyl incidents were also reviewed and provide some meaningful insight into decontamination at major urban areas. In order to proceed with decontamination, the item being processed needs to have an intrinsic value that exceeds the cost of the cleaning and justifies the exposure of any workers during the decontamination process(es). In the case of an entire building, the value may be obvious; it's costly to replace the structure. For a smaller item such as a vehicle or painting, the cost versus benefit of decontamination needs to be evaluated. This will be determined on a case by case basis and again is beyond the scope of this report, although some thoughts on decontamination of unique, personal and high value items are given. But, this is clearly an area that starting discussions and negotiations early on will greatly benefit both the economics and timeliness of the clean up. In addition, high value assets might benefit from pre-event protection such as protective coatings or HEPA filtered rooms to prevent contaminated outside air from entering the room (e.g., an art museum).

Heiser,J.; Sullivan, T.

2009-06-30T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


281

Optical Constants ofOptical Constants of Uranium Nitride Thin FilmsUranium Nitride Thin Films  

E-Print Network [OSTI]

Optical Constants ofOptical Constants of Uranium Nitride Thin FilmsUranium Nitride Thin FilmsDelta--Beta Scatter Plot at 220 eVBeta Scatter Plot at 220 eV #12;Why Uranium Nitride?Why Uranium Nitride? UraniumUranium, uranium,Bombard target, uranium, with argon ionswith argon ions Uranium atoms leaveUranium atoms leave

Hart, Gus

282

Proceedings of the workshop on transite decontamination dismantlement and recycle/disposal  

SciTech Connect (OSTI)

On February 3--4, 1993, a workshop was conducted to examine issues associated with the decontamination, dismantlement, and recycle/disposal of transite located at the US Department of Energy Fernald site near Cincinnati, OH. The Fernald Environmental Management Project (FEMP) is a Superfund Site currently undergoing remediation. A major objective of the workshop was to assess the state-of-the-art of transite remediation, and generate concepts that could be useful to the Fernald Environmental Restoration Management Co. (FERMCO) for remediation of transite. Transite is a building material consisting of asbestos fiber and cement and may be radioactively contaminated as a result of past uranium processing operations at the FEMP. Many of the 100 buildings within the former uranium production area were constructed of transite siding and roofing and consequently, over 180,000 m{sup 2} of transite must be disposed or recycled. Thirty-six participants representing industry, academia, and government institutions such as the EPA and DOE assembled at the workshop to present their experience with transite, describe work in progress, and address the issues involved in remediating transite.

Not Available

1993-12-31T23:59:59.000Z

283

Engineering evaluation/cost analysis for decontamination at the St. Louis Downtown Site, St. Louis, Missouri  

SciTech Connect (OSTI)

The US Department of Energy (DOE) is implementing a cleanup program for three groups of properties in the St. Louis, Missouri, area: the St. Louis Downtown Site (SLDS), the St. Louis Airport Site (SLAPS) and vicinity properties, and the Latty Avenue Properties, including the Hazelwood Interim Storage Site (HISS). The general location of these properties is shown in Figure 1; the properties are referred to collectively as the St. Louis Site. None of the properties are owned by DOE, but each property contains radioactive residues from federal uranium processing activities conducted at the SLDS during and after World War 2. The activities addressed in this environmental evaluation/cost analysis (EE/CA) report are being proposed as interim components of a comprehensive cleanup strategy for the St. Louis Site. As part of the Department's Formerly Utilized Sites Remedial Action Program (FUSRAP), DOE is proposing to conduct limited decontamination in support of proprietor-initiated activities at the SLDS, commonly referred to as the Mallinckrodt Chemical Works. The primary goal of FUSRAP activity at the SLDS is to eliminate potential environmental hazards associated with residual contamination resulting from the site's use for government-funded uranium processing activities. 17 refs., 3 figs., 5 tabs.

Picel, M.H.; Hartmann, H.M.; Nimmagadda, M.R. (Argonne National Lab., IL (USA)); Williams, M.J. (Bechtel National, Inc., Oak Ridge, TN (USA))

1991-05-01T23:59:59.000Z

284

Decontamination, decommissioning, and vendor advertorial issue, 2008  

SciTech Connect (OSTI)

The focus of the July-August issue is on Decontamination, decommissioning, and vendor advertorials. Articles and reports in this issue include: D and D technical paper summaries; The role of nuclear power in turbulent times, by Tom Chrisopher, AREVA, NP, Inc.; Enthusiastic about new technologies, by Jack Fuller, GE Hitachi Nuclear Energy; It's important to be good citizens, by Steve Rus, Black and Veatch Corporation; Creating Jobs in the U.S., by Guy E. Chardon, ALSTOM Power; and, and, An enviroment and a community champion, by Tyler Lamberts, Entergy Nuclear Operations, Inc. The Industry Innovations article is titled Best of the best TIP achievement 2008, by Edward Conaway, STP Nuclear Operating Company.

Agnihotri, Newal (ed.)

2008-07-15T23:59:59.000Z

285

Radioactive hot cell access hole decontamination machine  

DOE Patents [OSTI]

Radioactive hot cell access hole decontamination machine. A mobile housing has an opening large enough to encircle the access hole and has a shielding door, with a door opening and closing mechanism, for uncovering and covering the opening. The housing contains a shaft which has an apparatus for rotating the shaft and a device for independently translating the shaft from the housing through the opening and access hole into the hot cell chamber. A properly sized cylindrical pig containing wire brushes and cloth or other disks, with an arrangement for releasably attaching it to the end of the shaft, circumferentially cleans the access hole wall of radioactive contamination and thereafter detaches from the shaft to fall into the hot cell chamber.

Simpson, William E. (Richland, WA)

1982-01-01T23:59:59.000Z

286

Decontamination Systems Information and Research Program  

SciTech Connect (OSTI)

The Decontamination Systems Information and Research Program at West Virginia University consists of research and development associated with hazardous waste remediation problems at the Department of Energy complex and elsewhere. This program seeks to facilitate expedited development and implementation of solutions to the nation`s hazardous waste clean-up efforts. By a unique combination of university research and private technology development efforts, new paths toward implementing technology and speeding clean-ups are achievable. Mechanisms include aggressive industrial tie-ins to academic development programs, expedited support of small business technology development efforts, enhanced linkages to existing DOE programs, and facilitated access to hazardous waste sites. The program topically falls into an information component, which includes knowledge acquisition, technology evaluation and outreach activities and an R and D component, which develops and implements new and improved technologies. Projects began in February 1993 due to initiation of a Cooperative Agreement between West Virginia University and the Department of Energy.

Berg, M.; Sack, W.A.; Gabr, M. [and others

1994-12-31T23:59:59.000Z

287

Surface Decontamination Using Laser Ablation Process - 12032  

SciTech Connect (OSTI)

A new decontamination method has been investigated and used during two demonstration stages by the Clean-Up Business Unit of AREVA. This new method is based on the use of a Laser beam to remove the contaminants present on a base metal surface. In this paper will be presented the type of Laser used during those tests but also information regarding the efficiency obtained on non-contaminated (simulated contamination) and contaminated samples (from the CEA and La Hague facilities). Regarding the contaminated samples, in the first case, the contamination was a quite thick oxide layer. In the second case, most of the contamination was trapped in dust and thin grease layer. Some information such as scanning electron microscopy (SEM), X-Ray scattering spectroscopy and decontamination factors (DF) will be provided in this paper. Laser technology appears to be an interesting one for the future of the D and D applications. As shown in this paper, the results in terms of efficiency are really promising and in many cases, higher than those obtained with conventional techniques. One of the most important advantages is that all those results have been obtained with no generation of secondary wastes such as abrasives, chemicals, or disks... Moreover, as mentioned in introduction, the Laser ablation process can be defined as a 'dry' process. This technology does not produce any liquid waste (as it can be the case with chemical process or HP water process...). Finally, the addition of a vacuum system allows to trap the contamination onto filters and thus avoiding any dissemination in the room where the process takes place. The next step is going to be a commercial use in 2012 in one of the La Hague buildings. (authors)

Moggia, Fabrice; Lecardonnel, Xavier; Damerval, Frederique [AREVA, Back End Business Group, Clean Up Business Unit (France)

2012-07-01T23:59:59.000Z

288

Experimental partitioning of uranium between liquid iron sulfide and liquid silicate: Implications for radioactivity in the Earth's core  

E-Print Network [OSTI]

Experimental partitioning of uranium between liquid iron sulfide and liquid silicate: Implications Measurable uranium (U) is found in metal sulfide liquids in equilibrium with molten silicate at conditions shows that K is depleted in the Earth by $50%, while U and Th are slightly enriched (Palme and O

Minarik, William

289

Welding of uranium and uranium alloys  

SciTech Connect (OSTI)

The major reported work on joining uranium comes from the USA, Great Britain, France and the USSR. The driving force for producing this technology base stems from the uses of uranium as a nuclear fuel for energy production, compact structures requiring high density, projectiles, radiation shielding, and nuclear weapons. This review examines the state-of-the-art of this technology and presents current welding process and parameter information. The welding metallurgy of uranium and the influence of microstructure on mechanical properties is developed for a number of the more commonly used welding processes.

Mara, G.L.; Murphy, J.L.

1982-03-26T23:59:59.000Z

290

Development of Novel Sorbents for Uranium Extraction from Seawater  

SciTech Connect (OSTI)

As the uranium resource in terrestrial ores is limited, it is difficult to ensure a long-term sustainable nuclear energy technology. The oceans contain approximately 4.5 billion tons of uranium, which is one thousand times the amount of uranium in terrestrial ores. Development of technologies to recover the uranium from seawater would greatly improve the uranium resource availability, sustaining the fuel supply for nuclear energy. Several methods have been previously evaluated including solvent extraction, ion exchange, flotation, biomass collection, and adsorption; however, none have been found to be suitable for reasons such as cost effectiveness, long term stability, and selectivity. Recent research has focused on the amidoxime functional group as a promising candidate for uranium sorption. Polymer beads and fibers have been functionalized with amidoxime functional groups, and uranium adsorption capacities as high as 1.5 g U/kg adsorbent have recently been reported with these types of materials. As uranium concentration in seawater is only ~3 ppb, great improvements to uranium collection systems must be made in order to make uranium extraction from seawater economically feasible. This proposed research intends to develop transformative technologies for economic uranium extraction from seawater. The Lin group will design advanced porous supports by taking advantage of recent breakthroughs in nanoscience and nanotechnology and incorporate high densities of well-designed chelators into such nanoporous supports to allow selective and efficient binding of uranyl ions from seawater. Several classes of nanoporous materials, including mesoporous silica nanoparticles (MSNs), mesoporous carbon nanoparticles (MCNs), meta-organic frameworks (MOFs), and covalent-organic frameworks (COFs), will be synthesized. Selective uranium-binding liagnds such as amidoxime will be incorporated into the nanoporous materials to afford a new generation of sorbent materials that will be evaluated for their uranium extraction efficiency. The initial testing of these materials for uranium binding will be carried out in the Lin group, but more detailed sorption studies will be carried out by Dr. Taylor-Pashow of Savannah River National Laboratory in order to obtain quantitative uranyl sorption selectivity and kinetics data for the proposed materials. The proposed nanostructured sorbent materials are expected to have higher binding capacities, enhanced extraction kinetics, optimal stripping efficiency for uranyl ions, and enhanced mechanical and chemical stabilities. This transformative research will significantly impact uranium extraction from seawater as well as benefit DOE’s efforts on environmental remediation by developing new materials and providing knowledge for enriching and sequestering ultralow concentrations of other metals.

Lin, Wenbin; Taylor-Pashow, Kathryn

2014-01-08T23:59:59.000Z

291

Pilot-scale treatability testing -- Recycle, reuse, and disposal of materials from decontamination and decommissioning activities: Soda blasting demonstration  

SciTech Connect (OSTI)

The US Department of Energy (DOE) is in the process of defining the nature and magnitude of decontamination and decommissioning (D and D) obligations at its sites. With disposal costs rising and available storage facilities decreasing, DOE is exploring and implementing new waste minimizing D and D techniques. Technology demonstrations are being conducted by LMES at a DOE gaseous diffusion processing plant, the K-25 Site, in Oak Ridge, Tennessee. The gaseous diffusion process employed at Oak Ridge separated uranium-235 from uranium ore for use in atomic weapons and commercial reactors. These activities contaminated concrete and other surfaces within the plant with uranium, technetium, and other constituents. The objective of current K-25 D and D research is to make available cost-effective and energy-efficient techniques to advance remediation and waste management methods at the K-25 Site and other DOE sites. To support this objective, O`Brien and Gere tested a decontamination system on K-25 Site concrete and steel surfaces contaminated with radioactive and hazardous waste. A scouring system has been developed that removes fixed hazardous and radioactive surface contamination and minimizes residual waste. This system utilizes an abrasive sodium bicarbonate medium that is projected at contaminated surfaces. It mechanically removes surface contamination while leaving the surface intact. Blasting residuals are captured and dissolved in water and treated using physical/chemical processes. Pilot-scale testing of this soda blasting system and bench and pilot-scale treatment of the generated residuals were conducted from December 1993 to September 1994.

NONE

1995-08-01T23:59:59.000Z

292

A Robust Infrastructure Design for Gas Centrifuge Enrichment Plant Unattended Online Enrichment Monitoring  

SciTech Connect (OSTI)

An online enrichment monitor (OLEM) is being developed to continuously measure the relative isotopic composition of UF6 in the unit header pipes of a gas centrifuge enrichment plant (GCEP). From a safeguards perspective, OLEM will provide early detection of a facility being misused for production of highly enriched uranium. OLEM may also reduce the number of samples collected for destructive assay and if coupled with load cell monitoring can provide isotope mass balance verification. The OLEM design includes power and network connections for continuous monitoring of the UF6 enrichment and state of health of the instrument. Monitoring the enrichment on all header pipes at a typical GCEP could require OLEM detectors on each of the product, tails, and feed header pipes. If there are eight process units, up to 24 detectors may be required at a modern GCEP. Distant locations, harsh industrial environments, and safeguards continuity of knowledge requirements all place certain demands on the network robustness and power reliability. This paper describes the infrastructure and architecture of an OLEM system based on OLEM collection nodes on the unit header pipes and power and network support nodes for groupings of the collection nodes. A redundant, self-healing communications network, distributed backup power, and a secure communications methodology. Two candidate technologies being considered for secure communications are the Object Linking and Embedding for Process Control Unified Architecture cross-platform, service-oriented architecture model for process control communications and the emerging IAEA Real-time And INtegrated STream-Oriented Remote Monitoring (RAINSTORM) framework to provide the common secure communication infrastructure for remote, unattended monitoring systems. The proposed infrastructure design offers modular, commercial components, plug-and-play extensibility for GCEP deployments, and is intended to meet the guidelines and requirements for unattended and remotely monitored safeguards systems.

Younkin, James R [ORNL; Rowe, Nathan C [ORNL; Garner, James R [ORNL

2012-01-01T23:59:59.000Z

293

EPA Update: NESHAP Uranium Activities  

E-Print Network [OSTI]

for underground uranium mining operations (Subpart B) EPA regulatory requirements for operating uranium mill for Underground Uranium Mining Operations (Subpart B) #12;5 EPA Regulatory Requirements for Underground Uranium uranium mines include: · Applies to 10,000 tons/yr ore production, or 100,000 tons/mine lifetime · Ambient

294

Uranium hexafluoride public risk  

SciTech Connect (OSTI)

The limiting value for uranium toxicity in a human being should be based on the concentration of uranium (U) in the kidneys. The threshold for nephrotoxicity appears to lie very near 3 {mu}g U per gram kidney tissue. There does not appear to be strong scientific support for any other improved estimate, either higher or lower than this, of the threshold for uranium nephrotoxicity in a human being. The value 3 {mu}g U per gram kidney is the concentration that results from a single intake of about 30 mg soluble uranium by inhalation (assuming the metabolism of a standard person). The concentration of uranium continues to increase in the kidneys after long-term, continuous (or chronic) exposure. After chronic intakes of soluble uranium by workers at the rate of 10 mg U per week, the concentration of uranium in the kidneys approaches and may even exceed the nephrotoxic limit of 3 {mu}g U per gram kidney tissue. Precise values of the kidney concentration depend on the biokinetic model and model parameters assumed for such a calculation. Since it is possible for the concentration of uranium in the kidneys to exceed 3 {mu}g per gram tissue at an intake rate of 10 mg U per week over long periods of time, we believe that the kidneys are protected from injury when intakes of soluble uranium at the rate of 10 mg U per week do not continue for more than two consecutive weeks. For long-term, continuous occupational exposure to low-level, soluble uranium, we recommend a reduced weekly intake limit of 5 mg uranium to prevent nephrotoxicity in workers. Our analysis shows that the nephrotoxic limit of 3 {mu}g U per gram kidney tissues is not exceeded after long-term, continuous uranium intake at the intake rate of 5 mg soluble uranium per week.

Fisher, D.R.; Hui, T.E.; Yurconic, M.; Johnson, J.R.

1994-08-01T23:59:59.000Z

295

Modification of the Decontamination Facility at the Kruemmel NPP - 13451  

SciTech Connect (OSTI)

In February 2009, Siempelkamp Nukleartechnik GmbH was awarded the contract for the design, manufacture, delivery and construction of a new Decontamination Facility in the controlled area for Kruemmel NPP. The new decontamination equipment has been installed according to the state of art of Kruemmel NPP. The existing space required the following modification, retrofitting and reconstruction works: - Demounting of the existing installation: to create space for the new facility it was necessary to dismantle the old facility. The concrete walls and ceilings were cut into sizes of no more than 400 kg for ease of handling. This enabled decontamination so largest possible amount could be released for recycling. All steel parts were cut into sizes fitting for iron-barred boxes, respecting the requirement to render the parts decontaminable and releasable. - Reconstructing a decontamination facility: Reconstruction of a decontamination box with separate air lock as access area for the decontamination of components and assemblies was conducted using pressurized air with abrasives (glass beads or steel shots). The walls were equipped with sound protection, the inner walls were welded gap-free to prevent the emergence of interstices and were equipped with changeable wear and tear curtains. Abrasive processing unit positioned underneath the dry blasting box adjacent to the two discharge hoppers. A switch has been installed for the separation of the glass beads and the steel shot. The glass beads are directed into a 200 l drum for the disposal. The steel shot was cleaned using a separator. The cleaned steel shot was routed via transportation devices to the storage container, making it available for further blasting operations. A decontamination box with separate air lock as access area for the decontamination of components and assemblies using high pressure water technology was provided by new construction. Water pressures between 160 bar and 800 bar can be selected. The inner walls are welded gap-free and all rough edges are rounded off. All wetted parts are steel grade 1.4301 or higher. In an extension to the high pressure water decontamination box, 2 ultrasonic ponds and one washing station for small components as provide by new construction. A long pond with 3.25 m length for the decontamination of large components (e.g. turbine blades, pump rotors, driving rods) was installed. For the handling heavy components, a 2 t crane was installed. New construction of a mechanical effluent treatment facility including oil separator was connected to the existing effluent storage tank provided by the customer. One exhaust air filtration system is provided for each decontamination box, with the following requirements. The exhaust air is sent back to the room (recirculated air system). Dry blasting box including raw separator with dust collection in 200 l drum, filter for suspended particles; High pressure water decontamination box and wet area with water separator, pre-separator, filter for suspended particles. Installation of a steel platform at building height +12.85 above the decontamination boxes + 8.50 m for the erection of the high pressure water facilities, the recirculating air filter system, the air compressor and the respiratory air supply unit. The aforementioned components are placed on the steel platform and have been encased in a sound-lowering and accessible manner. New construction of the entire E and C technology for the TU system including modification of the supply lines from the switch gear. All devices are to be operated automatically. Dry blasting box, high pressure water decontamination box and wet area are designed to guarantee a unitary 'exterior view' of the decontamination facility. (authors)

Klute, Stefan; Kupke, Peter [Siempelkamp Nukleartechnik GmbH Am Taubenfeld 25/1, 69123 Heidelberg (Germany)] [Siempelkamp Nukleartechnik GmbH Am Taubenfeld 25/1, 69123 Heidelberg (Germany)

2013-07-01T23:59:59.000Z

296

Decontamination of water using nitrate selective ion exchange resin  

DOE Patents [OSTI]

A method for nitrate decontamination of water which involves passing the water through a bed of alkyl phosphonium anion exchange resin which has pendant alkyl groups of C[sub 3] or larger.

Lockridge, J.E.; Fritz, J.S.

1990-07-31T23:59:59.000Z

297

Enhanced toxic cloud knockdown spray system for decontamination applications  

DOE Patents [OSTI]

Methods and systems for knockdown and neutralization of toxic clouds of aerosolized chemical or biological warfare (CBW) agents and toxic industrial chemicals using a non-toxic, non-corrosive aqueous decontamination formulation.

Betty, Rita G. (Rio Rancho, NM); Tucker, Mark D. (Albuquerque, NM); Brockmann, John E. (Albuquerque, NM); Lucero, Daniel A. (Albuquerque, NM); Levin, Bruce L. (Tijeras, NM); Leonard, Jonathan (Albuquerque, NM)

2011-09-06T23:59:59.000Z

298

Y-12 Plant decontamination and decommissioning Technology Logic Diagram for Building 9201-4: Volume 3, Technology evaluation data sheets: Part B, Decontamination; robotics/automation; waste management  

SciTech Connect (OSTI)

This volume consists of the Technology Logic Diagrams (TLDs) for the decontamination, robotics/automation, and waste management areas.

NONE

1994-09-01T23:59:59.000Z

299

The Enriched Xenon Observatory  

SciTech Connect (OSTI)

The Enriched Xenon Observatory (EXO) experiment will search for neutrinoless double beta decay of {sup 136}Xe. The EXO Collaboration is actively pursuing both liquid-phase and gas-phase Xe detector technologies with scalability to the ton-scale. The search for neutrinoless double beta decay of {sup 136}Xe is especially attractive because of the possibility of tagging the resulting Ba daughter ion, eliminating all sources of background other than the two neutrino decay mode. EXO-200, the first phase of the project, is a liquid Xe time projection chamber with 200 kg of Xe enriched to 80% in {sup 136}Xe. EXO-200, which does not include Ba-tagging, will begin taking data in 2009, with two-year sensitivity to the half-life for neutrinoless double beta decay of 6.4x10{sup 25} years. This corresponds to an effective Majorana neutrino mass of 0.13 to 0.19 eV.

Dolinski, M. J. [Stanford University Physics Department, 382 Via Pueblo Mall, Stanford, CA 94305-4060 (United States)

2009-12-17T23:59:59.000Z

300

Occupational exposures to uranium: processes, hazards, and regulations  

SciTech Connect (OSTI)

The United States Uranium Registry (USUR) was formed in 1978 to investigate potential hazards from occupational exposure to uranium and to assess the need for special health-related studies of uranium workers. This report provides a summary of Registry work done to date. The history of the uranium industry is outlined first, and the current commercial uranium industry (mining, milling, conversion, enrichment, and fuel fabrication) is described. This description includes information on basic processes and areas of greatest potential radiological exposure. In addition, inactive commercial facilities and other uranium operations are discussed. Regulation of the commercial production industry for uranium fuel is reported, including the historic development of regulations and the current regulatory agencies and procedures for each phase of the industry. A review of radiological health practices in the industry - facility monitoring, exposure control, exposure evaluation, and record-keeping - is presented. A discussion of the nonradiological hazards of the industry is provided, and the final section describes the tissue program developed as part of the Registry.

Stoetzel, G.A.; Fisher, D.R.; McCormack, W.D.; Hoenes, G.R.; Marks, S.; Moore, R.H.; Quilici, D.G.; Breitenstein, B.D.

1981-04-01T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


301

A survey of decontamination processes applicable to DOE nuclear facilities  

SciTech Connect (OSTI)

The objective of this survey was to select an appropriate technology for in situ decontamination of equipment interiors as part of the decommissioning of U.S. Department of Energy nuclear facilities. This selection depends on knowledge of existing chemical decontamination methods. This report provides an up-to-date review of chemical decontamination methods. According to available information, aqueous systems are probably the most universally used method for decontaminating and cleaning metal surfaces. We have subdivided the technologies, on the basis of the types of chemical solvents, into acid, alkaline permanganate, highly oxidizing, peroxide, and miscellaneous systems. Two miscellaneous chemical decontamination methods (electrochemical processes and foam and gel systems) are also described. A concise technical description of various processes is given, and the report also outlines technical considerations in the choice of technologies, including decontamination effectiveness, waste handing, fields of application, and the advantages and limitations in application. On the basis of this survey, six processes were identified for further evaluation. 144 refs., 2 tabs.

Chen, L.; Chamberlain, D.B.; Conner, C.; Vandegrift, G.F.

1997-05-01T23:59:59.000Z

302

Anthrax Sampling and Decontamination: Technology Trade-Offs  

SciTech Connect (OSTI)

The goal of this project was to answer the following questions concerning response to a future anthrax release (or suspected release) in a building: 1. Based on past experience, what rules of thumb can be determined concerning: (a) the amount of sampling that may be needed to determine the extent of contamination within a given building; (b) what portions of a building should be sampled; (c) the cost per square foot to decontaminate a given type of building using a given method; (d) the time required to prepare for, and perform, decontamination; (e) the effectiveness of a given decontamination method in a given type of building? 2. Based on past experience, what resources will be spent on evaluating the extent of contamination, performing decontamination, and assessing the effectiveness of the decontamination in abuilding of a given type and size? 3. What are the trade-offs between cost, time, and effectiveness for the various sampling plans, sampling methods, and decontamination methods that have been used in the past?

Price, Phillip N.; Hamachi, Kristina; McWilliams, Jennifer; Sohn, Michael D.

2008-09-12T23:59:59.000Z

303

Uranium Mill Tailings Management  

SciTech Connect (OSTI)

This book presents the papers given at the Fifth Symposium on Uranium Mill Tailings Management. Advances made with regard to uranium mill tailings management, environmental effects, regulations, and reclamation are reviewed. Topics considered include tailings management and design (e.g., the Uranium Mill Tailings Remedial Action Project, environmental standards for uranium mill tailings disposal), surface stabilization (e.g., the long-term stability of tailings, long-term rock durability), radiological aspects (e.g. the radioactive composition of airborne particulates), contaminant migration (e.g., chemical transport beneath a uranium mill tailings pile, the interaction of acidic leachate with soils), radon control and covers (e.g., radon emanation characteristics, designing surface covers for inactive uranium mill tailings), and seepage and liners (e.g., hydrologic observations, liner requirements).

Nelson, J.D.

1982-01-01T23:59:59.000Z

304

Process for continuous production of metallic uranium and uranium alloys  

DOE Patents [OSTI]

A method is described for forming metallic uranium, or a uranium alloy, from uranium oxide in a manner which substantially eliminates the formation of uranium-containing wastes. A source of uranium dioxide is first provided, for example, by reducing uranium trioxide (UO{sub 3}), or any other substantially stable uranium oxide, to form the uranium dioxide (UO{sub 2}). This uranium dioxide is then chlorinated to form uranium tetrachloride (UCl{sub 4}), and the uranium tetrachloride is then reduced to metallic uranium by reacting the uranium chloride with a metal which will form the chloride of the metal. This last step may be carried out in the presence of another metal capable of forming one or more alloys with metallic uranium to thereby lower the melting point of the reduced uranium product. The metal chloride formed during the uranium tetrachloride reduction step may then be reduced in an electrolysis cell to recover and recycle the metal back to the uranium tetrachloride reduction operation and the chlorine gas back to the uranium dioxide chlorination operation. 4 figs.

Hayden, H.W. Jr.; Horton, J.A.; Elliott, G.R.B.

1995-06-06T23:59:59.000Z

305

Process for continuous production of metallic uranium and uranium alloys  

DOE Patents [OSTI]

A method is described for forming metallic uranium, or a uranium alloy, from uranium oxide in a manner which substantially eliminates the formation of uranium-containing wastes. A source of uranium dioxide is first provided, for example, by reducing uranium trioxide (UO.sub.3), or any other substantially stable uranium oxide, to form the uranium dioxide (UO.sub.2). This uranium dioxide is then chlorinated to form uranium tetrachloride (UCl.sub.4), and the uranium tetrachloride is then reduced to metallic uranium by reacting the uranium chloride with a metal which will form the chloride of the metal. This last step may be carried out in the presence of another metal capable of forming one or more alloys with metallic uranium to thereby lower the melting point of the reduced uranium product. The metal chloride formed during the uranium tetrachloride reduction step may then be reduced in an electrolysis cell to recover and recycle the metal back to the uranium tetrachloride reduction operation and the chlorine gas back to the uranium dioxide chlorination operation.

Hayden, Jr., Howard W. (Oakridge, TN); Horton, James A. (Livermore, CA); Elliott, Guy R. B. (Los Alamos, NM)

1995-01-01T23:59:59.000Z

306

Preparation of uranium compounds  

DOE Patents [OSTI]

UI.sub.3(1,4-dioxane).sub.1.5 and UI.sub.4(1,4-dioxane).sub.2, were synthesized in high yield by reacting turnings of elemental uranium with iodine dissolved in 1,4-dioxane under mild conditions. These molecular compounds of uranium are thermally stable and excellent precursor materials for synthesizing other molecular compounds of uranium including alkoxide, amide, organometallic, and halide compounds.

Kiplinger, Jaqueline L; Montreal, Marisa J; Thomson, Robert K; Cantat, Thibault; Travia, Nicholas E

2013-02-19T23:59:59.000Z

307

THE ENERGY SPECTRA OF URANIUM ATOMS SPUTTERED FROM URANIUM METAL AND URANIUM DIOXIDE TARGETS  

E-Print Network [OSTI]

THE ENERGY SPECTRA OF URANIUM ATOMS SPUTTERED FROM URANIUM METAL AND URANIUM DIOXIDE TARGETS Thesis. I have benefitted from conversations with many persons w~ile engaged in this project. I would like

Winfree, Erik

308

Kit systems for granulated decontamination formulations  

DOE Patents [OSTI]

A decontamination formulation and method of making that neutralizes the adverse health effects of both chemical and biological compounds, especially chemical warfare (CW) and biological warfare (BW) agents, and toxic industrial chemicals. The formulation provides solubilizing compounds that serve to effectively render the chemical and biological compounds, particularly CW and BW compounds, susceptible to attack, and at least one reactive compound that serves to attack (and detoxify or kill) the compound. The formulation includes at least one solubilizing agent, a reactive compound, a sorbent additive, and water. A highly adsorbent sorbent additive (e.g., amorphous silica, sorbitol, mannitol, etc.) is used to "dry out" one or more liquid ingredients into a dry, free-flowing powder that has an extended shelf life, and is more convenient to handle and mix in the field. The formulation can be pre-mixed and pre-packaged as a multi-part kit system, where one or more of the parts are packaged in a powdered, granulated form for ease of handling and mixing in the field.

Tucker, Mark D. (Albuquerque, NM)

2010-07-06T23:59:59.000Z

309

Mobile workstation for decontamination and decommissioning operations  

SciTech Connect (OSTI)

This project is an interdisciplinary effort to develop effective mobile worksystems for decontamination and decommissioning (D&D) of facilities within the DOE Nuclear Weapons Complex. These mobile worksystems will be configured to operate within the environmental and logistical constraints of such facilities and to perform a number of work tasks. Our program is designed to produce a mobile worksystem with capabilities and features that are matched to the particular needs of D&D work by evolving the design through a series of technological developments, performance tests and evaluations. The project has three phases. In this the first phase, an existing teleoperated worksystem, the Remote Work Vehicle (developed for use in the Three Mile Island Unit 2 Reactor Building basement), was enhanced for telerobotic performance of several D&D operations. Its ability to perform these operations was then assessed through a series of tests in a mockup facility that contained generic structures and equipment similar to those that D&D work machines will encounter in DOE facilities. Building upon the knowledge gained through those tests and evaluations, a next generation mobile worksystem, the RWV II, and a more advanced controller will be designed, integrated and tested in the second phase, which is scheduled for completion in January 1995. The third phase of the project will involve testing of the RWV II in the real DOE facility.

Whittaker, W.L.; Osborn, J.F.; Thompson, B.R. [Carnegie-Mellon Univ., Pittsburgh, PA (United States). Robotics Inst.

1993-10-01T23:59:59.000Z

310

Gas centrifuge enrichment plants inspection frequency and remote monitoring issues for advanced safeguards implementation  

SciTech Connect (OSTI)

Current safeguards approaches used by the IAEA at gas centrifuge enrichment plants (GCEPs) need enhancement in order to verify declared low enriched uranium (LEU) production, detect undeclared LEU production and detect high enriched uranium (BEU) production with adequate probability using non destructive assay (NDA) techniques. At present inspectors use attended systems, systems needing the presence of an inspector for operation, during inspections to verify the mass and {sup 235}U enrichment of declared cylinders of uranium hexafluoride that are used in the process of enrichment at GCEPs. This paper contains an analysis of how possible improvements in unattended and attended NDA systems including process monitoring and possible on-site destructive analysis (DA) of samples could reduce the uncertainty of the inspector's measurements providing more effective and efficient IAEA GCEPs safeguards. We have also studied a few advanced safeguards systems that could be assembled for unattended operation and the level of performance needed from these systems to provide more effective safeguards. The analysis also considers how short notice random inspections, unannounced inspections (UIs), and the concept of information-driven inspections can affect probability of detection of the diversion of nuclear material when coupled to new GCEPs safeguards regimes augmented with unattended systems. We also explore the effects of system failures and operator tampering on meeting safeguards goals for quantity and timeliness and the measures needed to recover from such failures and anomalies.

Boyer, Brian David [Los Alamos National Laboratory; Erpenbeck, Heather H [Los Alamos National Laboratory; Miller, Karen A [Los Alamos National Laboratory; Ianakiev, Kiril D [Los Alamos National Laboratory; Reimold, Benjamin A [Los Alamos National Laboratory; Ward, Steven L [Los Alamos National Laboratory; Howell, John [GLASGOW UNIV.

2010-09-13T23:59:59.000Z

311

Oxygen enriched fireflooding  

SciTech Connect (OSTI)

Both pure oxygen and enriched air have been considered in fireflooding for enhanced oil recovery. Laboratory and field testing have conclusively shown that oxygen is practical and cost effective for this application. For reservoirs that require a large volume of high pressure gas, oxygen is cheaper than air simply based on compression costs. Additional process benefits with oxygen include: Faster Oil Production; Lower Injection Pressure; Greater Well Spacing; Increased Carbon Dioxide Partial Pressure; Lower Gas-to-Oil Ratios; and Purer Produced Gas. These features provide a compelling case for oxygen, once the safety and materials compatibility issues are properly addressed.

Shahani, G.H.; Gunardson, H.H. [Air Products and Chemicals, Allentown, PA (United States)

1995-02-01T23:59:59.000Z

312

Uranium industry annual 1993  

SciTech Connect (OSTI)

Uranium production in the United States has declined dramatically from a peak of 43.7 million pounds U{sub 3}O{sub 8} (16.8 thousand metric tons uranium (U)) in 1980 to 3.1 million pounds U{sub 3}O{sub 8} (1.2 thousand metric tons U) in 1993. This decline is attributed to the world uranium market experiencing oversupply and intense competition. Large inventories of uranium accumulated when optimistic forecasts for growth in nuclear power generation were not realized. The other factor which is affecting U.S. uranium production is that some other countries, notably Australia and Canada, possess higher quality uranium reserves that can be mined at lower costs than those of the United States. Realizing its competitive advantage, Canada was the world`s largest producer in 1993 with an output of 23.9 million pounds U{sub 3}O{sub 8} (9.2 thousand metric tons U). The U.S. uranium industry, responding to over a decade of declining market prices, has downsized and adopted less costly and more efficient production methods. The main result has been a suspension of production from conventional mines and mills. Since mid-1992, only nonconventional production facilities, chiefly in situ leach (ISL) mining and byproduct recovery, have operated in the United States. In contrast, nonconventional sources provided only 13 percent of the uranium produced in 1980. ISL mining has developed into the most cost efficient and environmentally acceptable method for producing uranium in the United States. The process, also known as solution mining, differs from conventional mining in that solutions are used to recover uranium from the ground without excavating the ore and generating associated solid waste. This article describes the current ISL Yang technology and its regulatory approval process, and provides an analysis of the factors favoring ISL mining over conventional methods in a declining uranium market.

Not Available

1994-09-01T23:59:59.000Z

313

DUSCOBS - a depleted-uranium silicate backfill for transport, storage, and disposal of spent nuclear fuel  

SciTech Connect (OSTI)

A Depleted Uranium Silicate COntainer Backfill System (DUSCOBS) is proposed that would use small, isotopically-depleted uranium silicate glass beads as a backfill material inside storage, transport, and repository waste packages containing spent nuclear fuel (SNF). The uranium silicate glass beads would fill all void space inside the package including the coolant channels inside SNF assemblies. Based on preliminary analysis, the following benefits have been identified. DUSCOBS improves repository waste package performance by three mechanisms. First, it reduces the radionuclide releases from SNF when water enters the waste package by creating a local uranium silicate saturated groundwater environment that suppresses (1) the dissolution and/or transformation of uranium dioxide fuel pellets and, hence, (2) the release of radionuclides incorporated into the SNF pellets. Second, the potential for long-term nuclear criticality is reduced by isotopic exchange of enriched uranium in SNF with the depleted uranium (DU) in the glass. Third, the backfill reduces radiation interactions between SNF and the local environment (package and local geology) and thus reduces generation of hydrogen, acids, and other chemicals that degrade the waste package system. In addition, the DUSCOBS improves the integrity of the package by acting as a packing material and ensures criticality control for the package during SNF storage and transport. Finally, DUSCOBS provides a potential method to dispose of significant quantities of excess DU from uranium enrichment plants at potential economic savings. DUSCOBS is a new concept. Consequently, the concept has not been optimized or demonstrated in laboratory experiments.

Forsberg, C.W.; Pope, R.B.; Ashline, R.C.; DeHart, M.D.; Childs, K.W.; Tang, J.S.

1995-11-30T23:59:59.000Z

314

A simplified model of decontamination by BWR steam suppression pools  

SciTech Connect (OSTI)

Phenomena that can decontaminate aerosol-laden gases sparging through steam suppression pools of boiling water reactors during reactor accidents are described. Uncertainties in aerosol properties, aerosol behavior within gas bubbles, and bubble behavior in plumes affect predictions of decontamination by steam suppression pools. Uncertainties in the boundary and initial conditions that are dictated by the progression of severe reactor accidents and that will affect predictions of decontamination by steam suppression pools are discussed. Ten parameters that characterize boundary and initial condition uncertainties, nine parameters that characterize aerosol property and behavior uncertainties, and eleven parameters that characterize uncertainties in the behavior of bubbles in steam suppression pools are identified. Ranges for the values of these parameters and subjective probability distributions for parametric values within the ranges are defined. These uncertain parameters are used in Monte Carlo uncertainty analyses to develop uncertainty distributions for the decontamination that can be achieved by steam suppression pools and the size distribution of aerosols that do emerge from such pools. A simplified model of decontamination by steam suppression pools is developed by correlating features of the uncertainty distributions for total decontamination factor, DF(total), mean size of emerging aerosol particles, d{sub p}, and the standard deviation of the emerging aerosol size distribution, {sigma}, with pool depth, H. Correlations of the median values of the uncertainty distributions are suggested as the best estimate of decontamination by suppression pools. Correlations of the 10 percentile and 90 percentile values of the uncertainty distributions characterize the uncertainty in the best estimates. 295 refs., 121 figs., 113 tabs.

Powers, D.A.

1997-05-01T23:59:59.000Z

315

CHARACTERIZATION OF URANIUM, URANIUM OXIDE AND SILICON MULTILAYER THIN FILMS  

E-Print Network [OSTI]

CHARACTERIZATION OF URANIUM, URANIUM OXIDE AND SILICON MULTILAYER THIN FILMS by David T. Oliphant. Woolley Dean, College of Physical and Mathematical Sciences #12;ABSTRACT CHARACTERIZATION OF URANIUM, URANIUM OXIDE AND SILICON MULTILAYER THIN FILMS David T. Oliphant Department of Physics and Astronomy

Hart, Gus

316

Uranium dioxide electrolysis  

DOE Patents [OSTI]

This is a single stage process for treating spent nuclear fuel from light water reactors. The spent nuclear fuel, uranium oxide, UO.sub.2, is added to a solution of UCl.sub.4 dissolved in molten LiCl. A carbon anode and a metallic cathode is positioned in the molten salt bath. A power source is connected to the electrodes and a voltage greater than or equal to 1.3 volts is applied to the bath. At the anode, the carbon is oxidized to form carbon dioxide and uranium chloride. At the cathode, uranium is electroplated. The uranium chloride at the cathode reacts with more uranium oxide to continue the reaction. The process may also be used with other transuranic oxides and rare earth metal oxides.

Willit, James L. (Batavia, IL); Ackerman, John P. (Prescott, AZ); Williamson, Mark A. (Naperville, IL)

2009-12-29T23:59:59.000Z

317

Oak Ridge National Laboratory Technology Logic Diagram. Volume 2, Technology Logic Diagram: Part A, Decontamination and Decommissioning  

SciTech Connect (OSTI)

This report documents activities of decontamination and decommissioning at ORNL. Topics discussed include general problems, waste types, containment, robotics automation and decontamination processes.

Not Available

1993-09-01T23:59:59.000Z

318

Selective Extraction of Uranium from Liquid or Supercritical Carbon Dioxide  

SciTech Connect (OSTI)

Current liquid-liquid extraction processes used in recycling irradiated nuclear fuel rely on (1) strong nitric acid to dissolve uranium oxide fuel, and (2) the use of aliphatic hydrocarbons as a diluent in formulating the solvent used to extract uranium. The nitric acid dissolution process is not selective. It dissolves virtually the entire fuel meat which complicates the uranium extraction process. In addition, a solvent washing process is used to remove TBP degradation products, which adds complexity to the recycling plant and increases the overall plant footprint and cost. A liquid or supercritical carbon dioxide (l/sc -CO2) system was designed to mitigate these problems. Indeed, TBP nitric acid complexes are highly soluble in l/sc -CO2 and are capable of extracting uranium directly from UO2, UO3 and U3O8 powders. This eliminates the need for total acid dissolution of the irradiated fuel. Furthermore, since CO2 is easily recycled by evaporation at room temperature and pressure, it eliminates the complex solvent washing process. In this report, we demonstrate: (1) A reprocessing scheme starting with the selective extraction of uranium from solid uranium oxides into a TBP-HNO3 loaded Sc-CO2 phase, (2) Back extraction of uranium into an aqueous phase, and (3) Conversion of recovered purified uranium into uranium oxide. The purified uranium product from step 3 can be disposed of as low level waste, or mixed with enriched uranium for use in a reactor for another fuel cycle. After an introduction on the concept and properties of supercritical fluids, we first report the characterization of the different oxides used for this project. Our extraction system and our online monitoring capability using UV-Vis absorbance spectroscopy directly in sc-CO2 is then presented. Next, the uranium extraction efficiencies and kinetics is demonstrated for different oxides and under different physical and chemical conditions: l/sc -CO2 pressure and temperature, TBP/HNO3 complex used, reductant or complexant used for selectivity, and ionic liquids used as supportive media. To complete the extraction and recovery cycle, we then demonstrate uranium back extraction from the TBP loaded sc-CO2 phase into an aqueous phase and the characterization of the uranium complex formed at the end of this process. Another aspect of this project was to limit proliferation risks by either co-extracting uranium and plutonium, or by leaving plutonium behind by selectively extracting uranium. We report that the former is easily achieved, since plutonium is in the tetravalent or hexavalent oxidation state in the oxidizing environment created by the TBP-nitric acid complex, and is therefore co-extracted. The latter is more challenging, as a reductant or complexant to plutonium has to be used to selectively extract uranium. After undertaking experiments on different reducing or complexing systems (e.g., AcetoHydroxamic Acid (AHA), Fe(II), ascorbic acid), oxalic acid was chosen as it can complex tetravalent actinides (Pu, Np, Th) in the aqueous phase while allowing the extraction of hexavalent uranium in the sc-CO2 phase. Finally, we show results using an alternative media to commonly used aqueous phases: ionic liquids. We show the dissolution of uranium in ionic liquids and its extraction using sc-CO2 with and without the presence of AHA. The possible separation of trivalent actinides from uranium is also demonstrated in ionic liquids using neodymium as a surrogate and diglycolamides as the extractant.

Farawila, Anne F.; O'Hara, Matthew J.; Wai, Chien M.; Taylor, Harry Z.; Liao, Yu-Jung

2012-07-31T23:59:59.000Z

319

MERCURY CONTAMINATED MATERIAL DECONTAMINATION METHODS: INVESTIGATION AND ASSESSMENT  

SciTech Connect (OSTI)

Over the years mercury has been recognized as having serious impacts on human health and the environment. This recognition has led to numerous studies that deal with the properties of various mercury forms, the development of methods to quantify and speciate the forms, fate and transport, toxicology studies, and the development of site remediation and decontamination technologies. This report reviews several critical areas that will be used in developing technologies for cleaning mercury from mercury-contaminated surfaces of metals and porous materials found in many DOE facilities. The technologies used for decontamination of water and mixed wastes (solid) are specifically discussed. Many technologies that have recently appeared in the literature are included in the report. Current surface decontamination processes have been reviewed, and the limitations of these technologies for mercury decontamination are discussed. Based on the currently available technologies and the processes published recently in the literature, several processes, including strippable coatings, chemical cleaning with iodine/iodide lixiviant, chemisorbing surface wipes with forager sponge and grafted cotton, and surface/pore fixation through amalgamation or stabilization, have been identified as potential techniques for decontamination of mercury-contaminated metal and porous surfaces. Their potential merits and applicability are discussed. Finally, two processes, strippable coatings and chemical cleaning with iodine/iodide lixiviant, were experimentally investigated in Phase II of this project.

M.A. Ebadian, Ph.D.

2001-01-01T23:59:59.000Z

320

Decontamination by cleaning with fluorocarbon surfactant solutions  

SciTech Connect (OSTI)

In the nuclear industry, facilities and their components inevitably become contaminated with radioactive materials. This report documents the application of a novel particle-removal process developed by Entropic Systems, Inc. (ESI), to decontaminate critical instruments and parts that are contaminated with small radioactive particles that adhere to equipment surfaces. The tests were performed as a cooperative effort between ESI and the Chemical Technology Division of the Oak Ridge National Laboratory (ORNL). ESI developed a new, environmentally compatible process to remove small particles from solid surfaces that is more effective than spraying or sonicating with CFC-113. This process uses inert perfluorinated liquids as working media; the liquids have zero ozone-depleting potential, are nontoxic and nonflammnable, and are generally recognized as nonhazardous materials. In the ESI process, parts to be cleaned are first sprayed or sonicated with a dilute solution of a high-molecular-weight fluorocarbon surfactant in an inert perfluorinated liquid to effect particle removal. The parts are then rinsed with the perfluorinated liquid to remove the fluorocarbon surfactant applied in the first step, and the residual rinse liquid is then evaporated from the parts into an air or nitrogen stream from which it is recovered. Nuclear contamination is inherently a surface phenomenon. The presence of radioactive particles is responsible for all ``smearable`` contamination and, if the radioactive particles are small enough, for some of the fixed contamination. Because radioactivity does not influence the physical chemistry of particle adhesion, the ESI process should be just as effective in removing radioactive particles as it is in removing nonradioactive particles.

Kaiser, R. [Entropic Systems, Inc., Winchester, MA (United States); Benson, C.E.; Meyers, E.S. [Oak Ridge National Lab., TN (United States); Vaughen, V.C.A. [Chemical Engineering and Safety Consulting Services, Knoxville, TN (United States)

1994-02-01T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


321

An extremely radioresistant green eukaryote for radionuclide bio-decontamination in the nuclear  

E-Print Network [OSTI]

of adaptation to extreme environments. Introduction Nuclear energy technologies generate radioactiveAn extremely radioresistant green eukaryote for radionuclide bio-decontamination in the nuclear Blignyabcd Nuclear activities generate radioactive elements which require processes for their decontamination

Boyer, Edmond

322

The Soviet uranium industry and exports of nuclear materials and services  

SciTech Connect (OSTI)

The USSR has been offering Western countries, through long-term contracts, services in the processing and enrichment of uranium for their nuclear power industries since 1973. Although known for some time from Western sources, this was confirmed by Boris Semyenov, First Deputy Chairman of the USSR State Committee for the Utilization of Atomic Energy, in 1989. Other sources state that the first service contract was signed in 1971, with initial deliveries beginning in 1973, and that altogether, there are now about 10-12 long-term contracts with firms in various Western European countries that extend to the year 2000 or in some cases to 2010. Although these services are said to remain the mainstay of business with the capitalist countries of the West, the export of enriched uranium materials produced from domestic ore began in 1988. Clients include firms in both the US and Western Europe. Evidently, the severe balance-of-payments problems in Soviet foreign trade operations in recent years have led the Soviets to push alternatives to oil exports as much as possible, notably metals and minerals and chemicals and fertilizers, and this has now extended to the Soviet uranium industry. The paper discusses the USSR uranium industry, uranium mining, uranium enrichment, and plutonium production.

Sagers, M.J.

1990-08-01T23:59:59.000Z

323

Systems analysis of decontamination options for civilian vehicles.  

SciTech Connect (OSTI)

The objective of this project, which was supported by the Department of Homeland Security (DHS) Science and Technology Directorate (S&T) Chemical and Biological Division (CBD), was to investigate options for the decontamination of the exteriors and interiors of vehicles in the civilian setting in order to restore those vehicles to normal use following the release of a highly toxic chemical. The decontamination of vehicles is especially challenging because they often contain sensitive electronic equipment, multiple materials some of which strongly adsorb chemical agents, and in the case of aircraft, have very rigid material compatibility requirements (i.e., they cannot be exposed to reagents that may cause even minor corrosion). A systems analysis approach was taken examine existing and future civilian vehicle decontamination capabilities.

Foltz, Greg W.; Hoette, Trisha Marie

2010-11-01T23:59:59.000Z

324

Testing and evaluation of electrokinetic decontamination of concrete  

SciTech Connect (OSTI)

The goals and objectives of the technical task plan (TTP) are to (1) describe the nature and extent of concrete contamination within the Department of Energy (DOE) complex and emerging and commercial technologies applicable to these problems; (2) to match technologies to the concrete problems and recommend up to four demonstrations; (3) to initiate recommended demonstrations; and (4) to continue investigation and evaluation of the application of electrokinetic decontamination processes to concrete. This document presents findings of experimental and theoretical studies of the electrokinetic decontamination (EK) process and their implications for field demonstrations. This effort is an extension of the work performed under TTP 142005, ``Electroosmotic Concrete Decontamination. The goals of this task were to determine the applicability of EK for treating contaminated concrete and, if warranted, to evaluate EK as a potential technology for demonstration. 62 refs.

DePaoli, D.W.; Harris, M.T.; Ally, M.R. [Oak Ridge National Lab., TN (United States). Chemical Technology Div.] [and others

1996-10-01T23:59:59.000Z

325

Operating and life-cycle costs for uranium-contaminated soil treatment technologies  

SciTech Connect (OSTI)

The development of a nuclear industry in the US required mining, milling, and fabricating a large variety of uranium products. One of these products was purified uranium metal which was used in the Savannah River and Hanford Site reactors. Most of this feed material was produced at the US Department of Energy (DOE) facility formerly called the Feed Materials Production Center at Fernald, Ohio. During operation of this facility, soils became contaminated with uranium from a variety of sources. To avoid disposal of these soils in low-level radioactive waste burial sites, increasing emphasis has been placed on the remediating soils contaminated with uranium and other radionuclides. To address remediation and management of uranium-contaminated soils at sites owned by DOE, the DOE Office of Technology Development (OTD) evaluates and compares the versatility, efficiency, and economics of various technologies that may be combined into systems designed to characterize and remediate uranium-contaminated soils. Each technology must be able to (1) characterize the uranium in soil, (2) decontaminate or remove uranium from soil, (3) treat or dispose of resulting waste streams, (4) meet necessary state and federal regulations, and (5) meet performance assessment objectives. The role of the performance assessment objectives is to provide the information necessary to conduct evaluations of the technologies. These performance assessments provide the basis for selecting the optimum system for remediation of large areas contaminated with uranium. One of the performance assessment tasks is to address the economics of full-scale implementation of soil treatment technologies. The cost of treating contaminated soil is one of the criteria used in the decision-making process for selecting remedial alternatives.

Douthat, D.M.; Armstrong, A.Q. [Oak Ridge National Lab., TN (United States). Health Sciences Research Div.; Stewart, R.N. [Univ. of Tennessee, Knoxville, TN (United States)

1995-09-01T23:59:59.000Z

326

Study of Transients in an Enrichment Closed Loop  

E-Print Network [OSTI]

In the present thesis a mathematic model is presented in order to describe the dynamic behavior inside a closed enrichment loop, the latter representing a single stage of an uranium gaseous diffusion enrichment cascade.The analytical model is turned into a numerical model, and implemented through a computational code.For the verification of the model, measurements were taken in an experimental circuit using air as the process fluid.This circuit was instrumented so as to register its characteristic thermohydraulic variables.The measured transients were simulated, comparing the numerical results with the experimental measurements.A good agreement between the characteristic setting times and the thermohydraulic parameters evolution was observed.Besides, other transients of two species separation were numerically analyzed, including setting times of each magnitude, behavior of each one of them during different transients, and redistribution of concentrations.

Fernandino, M

2002-01-01T23:59:59.000Z

327

Process for decontaminating radioactive liquids using a calcium cyanamide-containing composition. [Patent application  

DOE Patents [OSTI]

The present invention provides a process for decontaminating a radioactive liquid containing a radioactive element capable of forming a hydroxide. This process includes the steps of contacting the radioactive liquid with a decontaminating composition and separating the resulting radioactive sludge from the resulting liquid. The decontaminating composition contains calcium cyanamide.

Silver, G.L.

1980-09-24T23:59:59.000Z

328

Depleted uranium management alternatives  

SciTech Connect (OSTI)

This report evaluates two management alternatives for Department of Energy depleted uranium: continued storage as uranium hexafluoride, and conversion to uranium metal and fabrication to shielding for spent nuclear fuel containers. The results will be used to compare the costs with other alternatives, such as disposal. Cost estimates for the continued storage alternative are based on a life-cycle of 27 years through the year 2020. Cost estimates for the recycle alternative are based on existing conversion process costs and Capital costs for fabricating the containers. Additionally, the recycle alternative accounts for costs associated with intermediate product resale and secondary waste disposal for materials generated during the conversion process.

Hertzler, T.J.; Nishimoto, D.D.

1994-08-01T23:59:59.000Z

329

Concrete decontamination by Electro-Hydraulic Scabbling (EHS)  

SciTech Connect (OSTI)

EHS is being developed for decontaminating concrete structures from radionuclides, organic substances, and hazardous metals. EHS involves the generation of powerful shock waves and intense cavitation by a strong pulsed electric discharge in a water layer at the concrete surface; high impulse pressure results in stresses which crack and peel off a concrete layer of controllable thickness. Scabbling produces contaminated debris of relatively small volume which can be easily removed, leaving clean bulk concrete. Objective of Phase I was to prove the technical feasibility of EH for controlled scabbling and decontamination of concrete. Phase I is complete.

NONE

1994-11-01T23:59:59.000Z

330

Safeguards Verification Measurements using Laser Ablation, Absorbance Ratio Spectrometry in Gaseous Centrifuge Enrichment Plants  

SciTech Connect (OSTI)

Laser Ablation Absorbance Ratio Spectrometry (LAARS) is a new verification measurement technology under development at the US Department of Energy (DOE) Pacific Northwest National Laboratory (PNNL). LAARS uses three lasers to ablate and then measure the relative isotopic abundance of uranium compounds. An ablation laser is tightly focused on uranium-bearing solids, producing a small atomic uranium vapor plume. Two collinear wavelength-tuned spectrometry lasers transit through the plume and the absorbance of U-235 and U-238 isotopes are measured to determine U-235 enrichment. The measurement is independent of chemical form and degree of dilution with nuisance dust and other materials. LAARS has high relative precision and detection limits approaching the femtogram range for U-235. The sample is scanned and assayed point-by-point at rates reaching 1 million measurements/hour, enabling LAARS to detect and analyze uranium in trace samples. The spectrometer is assembled using primarily commercially available components and features a compact design and automated analysis.Two specific gaseous centrifuge enrichment plant (GCEP) applications of the spectrometer are currently under development: 1) LAARS-Environmental Sampling (ES), which collects and analyzes aerosol particles for GCEP misuse detection and 2) LAARS-Destructive Assay (DA), which enables onsite enrichment DA sample collection and analysis for protracted diversion detection. The two applications propose game-changing technological advances in GCEP safeguards verification.

Anheier, Norman C.; Cannon, Bret D.; Kulkarni, Gourihar R.; Munley, John T.; Nelson, Danny A.; Qiao, Hong (Amy) [Amy; Phillips, Jon R.

2012-07-17T23:59:59.000Z

331

Irradiation behavior of miniature experimental uranium silicide fuel plates  

SciTech Connect (OSTI)

Uranium silicides, because of their relatively high uranium density, were selected as candidate dispersion fuels for the higher fuel densities required in the Reduced Enrichment Research and Test Reactor (RERTR) Program. Irradiation experience with this type of fuel, however, was limited to relatively modest fission densities in the bulk from, on the order of 7 x 10/sup 20/ cm/sup -3/, far short of the approximately 20 x 10/sup 20/ cm/sup -3/ goal established for the RERTR program. The purpose of the irradiation experiments on silicide fuels on the ORR, therefore, was to investigate the intrinsic irradiation behavior of uranium silicide as a dispersion fuel. Of particular interest was the interaction between the silicide particles and the aluminum matrix, the swelling behavior of the silicide particles, and the maximum volume fraction of silicide particles that could be contained in the aluminum matrix.

Hofman, G.L.; Neimark, L.A.; Mattas, R.F.

1983-01-01T23:59:59.000Z

332

Enrichment Assay Methods Development for the Integrated Cylinder Verification System  

SciTech Connect (OSTI)

International Atomic Energy Agency (IAEA) inspectors currently perform periodic inspections at uranium enrichment plants to verify UF6 cylinder enrichment declarations. Measurements are typically performed with handheld high-resolution sensors on a sampling of cylinders taken to be representative of the facility's entire product-cylinder inventory. Pacific Northwest National Laboratory (PNNL) is developing a concept to automate the verification of enrichment plant cylinders to enable 100 percent product-cylinder verification and potentially, mass-balance calculations on the facility as a whole (by also measuring feed and tails cylinders). The Integrated Cylinder Verification System (ICVS) could be located at key measurement points to positively identify each cylinder, measure its mass and enrichment, store the collected data in a secure database, and maintain continuity of knowledge on measured cylinders until IAEA inspector arrival. The three main objectives of this FY09 project are summarized here and described in more detail in the report: (1) Develop a preliminary design for a prototype NDA system, (2) Refine PNNL's MCNP models of the NDA system, and (3) Procure and test key pulse-processing components. Progress against these tasks to date, and next steps, are discussed.

Smith, Leon E.; Misner, Alex C.; Hatchell, Brian K.; Curtis, Michael M.

2009-10-22T23:59:59.000Z

333

Defining the needs for gas centrifuge enrichment plants advanced safeguards  

SciTech Connect (OSTI)

Current safeguards approaches used by the International Atomic Energy Agency (IAEA) at gas centrifuge enrichment plants (GCEPs) need enhancement in order to verify declared low-enriched (LEU) production, detect undeclared LEU production and detect highly enriched uranium (HEU) production with adequate detection probability using nondestructive assay (NDA) techniques. At present inspectors use attended systems, systems needing the presence of an inspector for operation, during inspections to verify the mass and {sup 235}U enrichment of declared UF{sub 6} containers used in the process of enrichment at GCEPs. In verifying declared LEU production, the inspectors also take samples for off-site destructive assay (DA) which provide accurate data, with 0.1% to 0.5% measurement uncertainty, on the enrichment of the UF{sub 6} feed, tails, and product. However, taking samples of UF{sub 6} for off-site analysis is a much more labor and resource intensive exercise for the operator and inspector. Furthermore, the operator must ship the samples off-site to the IAEA laboratory which delays the timeliness of results and interruptions to the continuity of knowledge (CofK) of the samples during their storage and transit. This paper contains an analysis of possible improvements in unattended and attended NDA systems such as process monitoring and possible on-site analysis of DA samples that could reduce the uncertainty of the inspector's measurements and provide more effective and efficient IAEA GCEPs safeguards. We also introduce examples advanced safeguards systems that could be assembled for unattended operation.

Boyer, Brian David [Los Alamos National Laboratory; Erpenbeck, Heather H [Los Alamos National Laboratory; Miller, Karen A [Los Alamos National Laboratory; Swinhoe, Martyn T [Los Alamos National Laboratory; Ianakiev, Kiril [Los Alamos National Laboratory; Marlow, Johnna B [Los Alamos National Laboratory

2010-04-05T23:59:59.000Z

334

Ultraslow Wave Nuclear Burning of Uranium-Plutonium Fissile Medium on Epithermal Neutrons  

E-Print Network [OSTI]

For a fissile medium, originally consisting of uranium-238, the investigation of fulfillment of the wave burning criterion in a wide range of neutron energies is conducted for the first time, and a possibility of wave nuclear burning not only in the region of fast neutrons, but also for cold, epithermal and resonance ones is discovered for the first time. For the first time the results of the investigation of the Feoktistov criterion fulfillment for a fissile medium, originally consisting of uranium-238 dioxide with enrichments 4.38%, 2.00%, 1.00%, 0.71% and 0.50% with respect to uranium-235, in the region of neutron energies 0.015-10.0eV are presented. These results indicate a possibility of ultraslow wave neutron-nuclear burning mode realization in the uranium-plutonium media, originally (before the wave initiation by external neutron source) having enrichments with respect to uranium-235, corresponding to the subcritical state, in the regions of cold, thermal, epithermal and resonance neutrons. In order to validate the conclusions, based on the slow wave neutron-nuclear burning criterion fulfillment depending on the neutron energy, the numerical modeling of ultraslow wave neutron-nuclear burning of a natural uranium in the epithermal region of neutron energies (0.1-7.0eV) was conducted for the first time. The presented simulated results indicate the realization of the ultraslow wave neutron-nuclear burning of the natural uranium for the epithermal neutrons.

V. D. Rusov; V. A. Tarasov; M. V. Eingorn; S. A. Chernezhenko; A. A. Kakaev; V. M. Vashchenko; M. E. Beglaryan

2014-09-29T23:59:59.000Z

335

Measurement and Analysis of Fission Rates in a Spherical Mockup of Uranium and Polyethylene  

E-Print Network [OSTI]

Measurements of the reaction rate distribution were carried out using two kinds of Plate Micro Fission Chamber(PMFC). The first is a depleted uranium chamber and the second an enriched uranium chamber. The material in the depleted uranium chamber is strictly the same as the material in the uranium assembly. With the equation solution to conduct the isotope contribution correction, the fission rate of 238U and 235U were obtained from the fission rate of depleted uranium and enriched uranium. And then, the fission count of 238U and 235U in an individual uranium shell was obtained. In this work, MCNP5 and continuous energy cross sections ENDF/BV.0 were used for the analysis of fission rate distribution and fission count. The calculated results were compared with the experimental ones. The calculation of fission rate of DU and EU were found to agree with the measured ones within 10% except at the positions in polyethylene region and the two positions near the outer surface. Beacause the fission chamber was not co...

Tong-Hua, Zhu; Xin-Xin, Lu; Rong, Liu; Zi-Jie, Han; Li, Jiang; Mei, Wang

2013-01-01T23:59:59.000Z

336

Method for the recovery of uranium values from uranium tetrafluoride  

DOE Patents [OSTI]

The invention is a novel method for the recovery of uranium from dry, particulate uranium tetrafluoride. In one aspect, the invention comprises reacting particulate uranium tetrafluoride and calcium oxide in the presence of gaseous oxygen to effect formation of the corresponding alkaline earth metal uranate and alkaline earth metal fluoride. The product uranate is highly soluble in various acidic solutions wherein the product fluoride is virtually insoluble therein. The product mixture of uranate and alkaline earth metal fluoride is contacted with a suitable acid to provide a uranium-containing solution, from which the uranium is recovered. The invention can achieve quantitative recovery of uranium in highly pure form.

Kreuzmann, Alvin B. (Cincinnati, OH)

1983-01-01T23:59:59.000Z

337

Method for the recovery of uranium values from uranium tetrafluoride  

DOE Patents [OSTI]

The invention is a novel method for the recovery of uranium from dry, particulate uranium tetrafluoride. In one aspect, the invention comprises reacting particulate uranium tetrafluoride and calcium oxide in the presence of gaseous oxygen to effect formation of the corresponding alkaline earth metal uranate and alkaline earth metal fluoride. The product uranate is highly soluble in various acidic solutions whereas the product fluoride is virtually insoluble therein. The product mixture of uranate and alkaline earth metal fluoride is contacted with a suitable acid to provide a uranium-containing solution, from which the uranium is recovered. The invention can achieve quantitative recovery of uranium in highly pure form.

Kreuzmann, A.B.

1982-10-27T23:59:59.000Z

338

Characterization of decontamination and decommissioning wastes expected from the major processing facilities in the 200 Areas  

SciTech Connect (OSTI)

This study was intended to characterize and estimate the amounts of equipment and other materials that are candidates for removal and subsequent processing in a solid waste facility when the major processing and handling facilities in the 200 Areas of the Hanford Site are decontaminated and decommissioned. The facilities in this study were selected based on processing history and on the magnitude of the estimated decommissioning cost cited in the Surplus Facilities Program Plan; Fiscal Year 1993 (Winship and Hughes 1992). The facilities chosen for this study include B Plant (221-B), T Plant (221-T), U Plant (221-U), the Uranium Trioxide (UO{sub 3}) Plant (224-U and 224-UA), the Reduction Oxidation (REDOX) or S Plant (202-S), the Plutonium Concentration Facility for B Plant (224-B), and the Concentration Facility for the Plutonium Finishing Plant (PFP) and REDOX (233-S). This information is required to support planning activities for current and future solid waste treatment, storage, and disposal operations and facilities.

Amato, L.C.; Franklin, J.D.; Hyre, R.A.; Lowy, R.M.; Millar, J.S.; Pottmeyer, J.A. [Los Alamos Technical Associates, Kennewick, WA (United States); Duncan, D.R. [Westinghouse Hanford Co., Richland, WA (United States)

1994-08-01T23:59:59.000Z

339

Graphite Waste Tank Cleanup and Decontamination under the Marcoule UP1 D and D Program - 13166  

SciTech Connect (OSTI)

The UP1 plant in Marcoule reprocessed nearly 20,000 tons of used natural uranium gas cooled reactor fuel coming from the first generation of civil nuclear reactors in France. During more than 40 years, the decladding operations produced thousands of tons of processed waste, mainly magnesium and graphite fragments. In the absence of a French repository for the graphite waste, the graphite sludge content of the storage pits had to be retrieved and transferred into a newer and safer pit. After an extensive R and D program, the equipment and process necessary for retrieval operations were designed, built and tested. The innovative process is mainly based on the use of two pumps (one to capture and the other one to transfer the sludge) working one after the other and a robotic arm mounted on a telescopic mast. A dedicated process was also set up for the removal of the biggest fragments. The retrieval of the most irradiating fragments was a challenge. Today, the first pit is totally empty and its stainless steel walls have been decontaminated using gels. In the second pit, the sludge retrieval and transfer operations have been almost completed. Most of the non-pumpable graphite fragments has been removed and transferred to a new storage pit. After more than 6 years of operations in sludge retrieval, a lot of experience was acquired from which important 'lessons learned' could be shared. (authors)

Thomasset, Philippe [AREVA D and D BU, Marcoule (France)] [AREVA D and D BU, Marcoule (France); Chabeuf, Jean-Michel [AREVA D and D BU, La Hague (France)] [AREVA D and D BU, La Hague (France); Thiebaut, Valerie [CEA/DEN/DAPD/CPUP, Marcoule (France)] [CEA/DEN/DAPD/CPUP, Marcoule (France); Chambon, Frederic [AREVA FEDERAL SERVICES, Columbia, MD (United States)] [AREVA FEDERAL SERVICES, Columbia, MD (United States)

2013-07-01T23:59:59.000Z

340

Advanced technologies for decontamination and conversion of scrap metal  

SciTech Connect (OSTI)

In October 1993, Manufacturing Sciences Corporation was awarded DOE contract DE-AC21-93MC30170 to develop and test recycling of radioactive scrap metal (RSM) to high value and intermediate and final product forms. This work was conducted to help solve the problems associated with decontamination and reuse of the diffusion plant barrier nickel and other radioactively contaminated scrap metals present in the diffusion plants. Options available for disposition of the nickel include decontamination and subsequent release or recycled product manufacture for restricted end use. Both of these options are evaluated during the course of this research effort. work during phase I of this project successfully demonstrated the ability to make stainless steel from barrier nickel feed. This paved the way for restricted end use products made from stainless steel. Also, after repeated trials and studies, the inducto-slag nickel decontamination process was eliminated as a suitable alternative. Electro-refining appeared to be a promising technology for decontamination of the diffusion plant barrier material. Goals for phase II included conducting experiments to facilitate the development of an electro-refining process to separate technetium from nickel. In parallel with those activities, phase II efforts were to include the development of the necessary processes to make useful products from radioactive scrap metal. Nickel from the diffusion plants as well as stainless steel and carbon steel could be used as feed material for these products.

MacNair, V.; Muth, T.; Shasteen, K.; Liby, A.; Hradil, G.; Mishra, B.

1996-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


341

COMPARING DETECTION METHODS OF AFLATOXIN AND EXPLORING AFLATOXIN DECONTAMINATION METHODS  

E-Print Network [OSTI]

DECONTAMINATION METHODS Pages in Study: 81 Candidate for Degree of Master of Science Ethanol fermentation if aflatoxin concentrated in the distilled ethanol and/or dry distillers grain end-products. Alliquots of fermented mash, distilled ethanol, stillage, and dry distillers grain (DDG) were analyzed via LC

Ray, David

342

Ris-R-1029(EN) Mechanical decontamination tests in  

E-Print Network [OSTI]

Risø-R-1029(EN) Mechanical decontamination tests in areas affected by the Chernobyl accident J % at the ground floor and by 27 % at the first floor. The soil around the houses was removed by a bobcat, while in the Area 23 Depth Distribution of 137 Cs in the Soil. 25 Type 27 Summary of Soil Contamination 29 Roof

343

Atmospheric-pressure plasma decontamination/sterilization chamber  

DOE Patents [OSTI]

An atmospheric-pressure plasma decontamination/sterilization chamber is described. The apparatus is useful for decontaminating sensitive equipment and materials, such as electronics, optics and national treasures, which have been contaminated with chemical and/or biological warfare agents, such as anthrax, mustard blistering agent, VX nerve gas, and the like. There is currently no acceptable procedure for decontaminating such equipment. The apparatus may also be used for sterilization in the medical and food industries. Items to be decontaminated or sterilized are supported inside the chamber. Reactive gases containing atomic and metastable oxygen species are generated by an atmospheric-pressure plasma discharge in a He/O.sub.2 mixture and directed into the region of these items resulting in chemical reaction between the reactive species and organic substances. This reaction typically kills and/or neutralizes the contamination without damaging most equipment and materials. The plasma gases are recirculated through a closed-loop system to minimize the loss of helium and the possibility of escape of aerosolized harmful substances.

Herrmann, Hans W. (Los Alamos, NM); Selwyn, Gary S. (Los Alamos, NM)

2001-01-01T23:59:59.000Z

344

The ultimate disposition of depleted uranium  

SciTech Connect (OSTI)

Significant amounts of the depleted uranium (DU) created by past uranium enrichment activities have been sold, disposed of commercially, or utilized by defense programs. In recent years, however, the demand for DU has become quite small compared to quantities available, and within the US Department of Energy (DOE) there is concern for any risks and/or cost liabilities that might be associated with the ever-growing inventory of this material. As a result, Martin Marietta Energy Systems, Inc. (Energy Systems), was asked to review options and to develop a comprehensive plan for inventory management and the ultimate disposition of DU accumulated at the gaseous diffusion plants (GDPs). An Energy Systems task team, under the chairmanship of T. R. Lemons, was formed in late 1989 to provide advice and guidance for this task. This report reviews options and recommends actions and objectives in the management of working inventories of partially depleted feed (PDF) materials and for the ultimate disposition of fully depleted uranium (FDU). Actions that should be considered are as follows. (1) Inspect UF{sub 6} cylinders on a semiannual basis. (2) Upgrade cylinder maintenance and storage yards. (3) Convert FDU to U{sub 3}O{sub 8} for long-term storage or disposal. This will include provisions for partial recovery of costs to offset those associated with DU inventory management and the ultimate disposal of FDU. Another recommendation is to drop the term tails'' in favor of depleted uranium'' or DU'' because the tails'' label implies that it is waste.'' 13 refs.

Not Available

1990-12-01T23:59:59.000Z

345

Relative performance properties of the ORNL Advanced Neutron Source Reactor with reduced enrichment fuels  

SciTech Connect (OSTI)

Three cores for the Advanced Neutron Source reactor, differing in size, enrichment, and uranium density in the fuel meat, have been analyzed. Performance properties of the reduced enrichment cores are compared with those of the HEU reference configuration. Core lifetime estimates suggest that none of these configurations will operate for the design goal of 17 days at 330 MW. With modes increases in fuel density and/or enrichment, however, the operating lifetimes of the HEU and MEU designs can be extended to the desired length. Achieving this lifetime with LEU fuel in any of the three studies cores, however, will require the successful development of denser fuels and/or structural materials with thermal neutron absorption cross sections substantially less than that of Al-6061. Relative to the HEU reference case, the peak thermal neutron flux in cores with reduced enrichment will be diminished by about 25--30%.

Bretscher, M.M.; Deen, J.R.; Hanan, N.A.; Matos, J.E.; Mo, S.C.; Pond, R.B.; Travelli, A.; Woodruff, W.L.

1994-12-31T23:59:59.000Z

346

Decontamination Processes for Restorative Operations and as a Precursor to Decommissioning: A Literature Review  

SciTech Connect (OSTI)

Pacific Northwest Laboratory (PNL) conducted an comprehensive literature review of actual reactor decontamination processes that are currently available. In general, any decontamination process should be based on the following criteria: effectiveness, efficiency, safety, and waste production. The information that was collected and analyzed has been divided into three major categories of decontamination: chemical, mechanical, and electrochemical. Chemical methods can be further classified as either low-concentration, singlestep processes or high-concentration, single- or multistep processes. Numerous chemical decontamination methods are detailed. Mechanical decontamination methods are usually restricted to the removal of a contaminated surface layer, whlch limits their versatility; several mechanical decontamination methods are described. Electrochemical decontamination. is both fast and easily controlled, and numerous processes that have been used in industry for many years are discussed. Information obtained from this work is tabulated in Appendix A for easy access, and a bibliography and a glossary have been provided.

Nelson, J. L.; Divine, J. R.

1981-05-01T23:59:59.000Z

347

Status Report on the Passive Neutron Enrichment Meter (PNEM) for UF6 Cylinder Assay  

SciTech Connect (OSTI)

The Passive Neutron Enrichment Meter (PNEM) is a nondestructive assay (NDA) system being developed at Los Alamos National Laboratory (LANL). It was designed to determine {sup 235}U mass and enrichment of uranium hexafluoride (UF{sub 6}) in product, feed, and tails cylinders (i.e., 30B and 48Y cylinders). These cylinders are found in the nuclear fuel cycle at uranium conversion, enrichment, and fuel fabrication facilities. The PNEM is a {sup 3}He-based neutron detection system that consists of two briefcase-sized detector pods. A photograph of the system during characterization at LANL is shown in Fig. 1. Several signatures are currently being studied to determine the most effective measurement and data reduction technique for unfolding {sup 235}U mass and enrichment. The system collects total neutron and coincidence data for both bare and cadmium-covered detector pods. The measurement concept grew out of the success of the Uranium Cylinder Assay System (UCAS), which is an operator system at Rokkasho Enrichment Plant (REP) that uses total neutron counting to determine {sup 235}U mass in UF{sub 6} cylinders. The PNEM system was designed with higher efficiency than the UCAS in order to add coincidence counting functionality for the enrichment determination. A photograph of the UCAS with a 48Y cylinder at REP is shown in Fig. 2, and the calibration measurement data for 30B product and 48Y feed and tails cylinders is shown in Fig. 3. The data was collected in a low-background environment, meaning there is very little scatter in the data. The PNEM measurement concept was first presented at the 2010 Institute of Nuclear Materials Management (INMM) Annual Meeting. The physics design and uncertainty analysis were presented at the 2010 International Atomic Energy Agency (IAEA) Safeguards Symposium, and the mechanical and electrical designs and characterization measurements were published in the ESARDA Bulletin in 2011.

Miller, Karen A. [Los Alamos National Laboratory; Swinhoe, Martyn T. [Los Alamos National Laboratory; Menlove, Howard O. [Los Alamos National Laboratory; Marlow, Johnna B. [Los Alamos National Laboratory

2012-05-02T23:59:59.000Z

348

Process for electrolytically preparing uranium metal  

DOE Patents [OSTI]

A process for making uranium metal from uranium oxide by first fluorinating uranium oxide to form uranium tetrafluoride and next electrolytically reducing the uranium tetrafluoride with a carbon anode to form uranium metal and CF.sub.4. The CF.sub.4 is reused in the fluorination reaction rather than being disposed of as a hazardous waste.

Haas, Paul A. (Knoxville, TN)

1989-01-01T23:59:59.000Z

349

Controlling uranium reactivity March 18, 2008  

E-Print Network [OSTI]

for the last decade. Most of their work involves depleted uranium, a more common form of uraniumMarch 2008 Controlling uranium reactivity March 18, 2008 Uranium is an often misunderstood metal uranium research. In reality, uranium presents a wealth of possibilities for funda- mental chemistry. Many

Meyer, Karsten

350

Influence of uranium hydride oxidation on uranium metal behaviour  

SciTech Connect (OSTI)

This work addresses concerns that the rapid, exothermic oxidation of active uranium hydride in air could stimulate an exothermic reaction (burning) involving any adjacent uranium metal, so as to increase the potential hazard arising from a hydride reaction. The effect of the thermal reaction of active uranium hydride, especially in contact with uranium metal, does not increase in proportion with hydride mass, particularly when considering large quantities of hydride. Whether uranium metal continues to burn in the long term is a function of the uranium metal and its surroundings. The source of the initial heat input to the uranium, if sufficient to cause ignition, is not important. Sustained burning of uranium requires the rate of heat generation to be sufficient to offset the total rate of heat loss so as to maintain an elevated temperature. For dense uranium, this is very difficult to achieve in naturally occurring circumstances. Areas of the uranium surface can lose heat but not generate heat. Heat can be lost by conduction, through contact with other materials, and by convection and radiation, e.g. from areas where the uranium surface is covered with a layer of oxidised material, such as burned-out hydride or from fuel cladding. These rates of heat loss are highly significant in relation to the rate of heat generation by sustained oxidation of uranium in air. Finite volume modelling has been used to examine the behaviour of a magnesium-clad uranium metal fuel element within a bottle surrounded by other un-bottled fuel elements. In the event that the bottle is breached, suddenly, in air, it can be concluded that the bulk uranium metal oxidation reaction will not reach a self-sustaining level and the mass of uranium oxidised will likely to be small in relation to mass of uranium hydride oxidised. (authors)

Patel, N.; Hambley, D. [National Nuclear Laboratory (United Kingdom); Clarke, S.A. [Sellafield Ltd (United Kingdom); Simpson, K.

2013-07-01T23:59:59.000Z

351

Analysis of the effectiveness of gas centrifuge enrichment plants advanced safeguards  

SciTech Connect (OSTI)

Current safeguards approaches used by the International Atomic Energy Agency (IAEA) at gas centrifuge enrichment plants (GCEPs) need enhancement in order to verify declared low-enriched uranium (LEU) production, detect undeclared LEU production and detect highly enriched uranium (HEU) production with adequate detection probability using non destructive assay (NDA) techniques. At present inspectors use attended systems, systems needing the presence of an inspector for operation, during inspections to verify the mass and 235U enrichment of declared UF6 containers used in the process of enrichment at GCEPs. This paper contains an analysis of possible improvements in unattended and attended NDA systems including process monitoring and possible on-site destructive assay (DA) of samples that could reduce the uncertainty of the inspector's measurements. These improvements could reduce the difference between the operator's and inspector's measurements providing more effective and efficient IAEA GCEPs safeguards. We also explore how a few advanced safeguards systems could be assembled for unattended operation. The analysis will focus on how unannounced inspections (UIs), and the concept of information-driven inspections (IDS) can affect probability of detection of the diversion of nuclear materials when coupled to new GCEPs safeguards regimes augmented with unattended systems.

Boyer, Brian David [Los Alamos National Laboratory; Erpenbeck, Heather H [Los Alamos National Laboratory; Miller, Karen A [Los Alamos National Laboratory; Swinjoe, Martyn T [Los Alamos National Laboratory; Ianakiev, Kiril D [Los Alamos National Laboratory; Marlow, Johnna B [Los Alamos National Laboratory

2010-01-01T23:59:59.000Z

352

Uranium-titanium-niobium alloy  

DOE Patents [OSTI]

A uranium alloy having small additions of Ti and Nb shows improved strength and ductility in cross section of greater than one inch over prior uranium alloy having only Ti as an alloying element.

Ludtka, Gail M. (Oak Ridge, TN); Ludtka, Gerard M. (Oak Ridge, TN)

1990-01-01T23:59:59.000Z

353

Uranium deposits of Brazil  

SciTech Connect (OSTI)

Brazil is a country of vast natural resources, including numerous uranium deposits. In support of the country`s nuclear power program, Brazil has developed the most active uranium industry in South America. Brazil has one operating reactor (Angra 1, a 626-MWe PWR), and two under construction. The country`s economic challenges have slowed the progress of its nuclear program. At present, the Pocos de Caldas district is the only active uranium production. In 1990, the Cercado open-pit mine produced approximately 45 metric tons (MT) U{sub 3}O{sub 8} (100 thousand pounds). Brazil`s state-owned uranium production and processing company, Uranio do Brasil, announced it has decided to begin shifting its production from the high-cost and nearly depleted deposits at Pocos de Caldas, to lower-cost reserves at Lagoa Real. Production at Lagoa Real is schedules to begin by 1993. In addition to these two districts, Brazil has many other known uranium deposits, and as a whole, it is estimated that Brazil has over 275,000 MT U{sub 3}O{sub 8} (600 million pounds U{sub 3}O{sub 8}) in reserves.

NONE

1991-09-01T23:59:59.000Z

354

Uranium hexafluoride handling. Proceedings  

SciTech Connect (OSTI)

The United States Department of Energy, Oak Ridge Field Office, and Martin Marietta Energy Systems, Inc., are co-sponsoring this Second International Conference on Uranium Hexafluoride Handling. The conference is offered as a forum for the exchange of information and concepts regarding the technical and regulatory issues and the safety aspects which relate to the handling of uranium hexafluoride. Through the papers presented here, we attempt not only to share technological advances and lessons learned, but also to demonstrate that we are concerned about the health and safety of our workers and the public, and are good stewards of the environment in which we all work and live. These proceedings are a compilation of the work of many experts in that phase of world-wide industry which comprises the nuclear fuel cycle. Their experience spans the entire range over which uranium hexafluoride is involved in the fuel cycle, from the production of UF{sub 6} from the naturally-occurring oxide to its re-conversion to oxide for reactor fuels. The papers furnish insights into the chemical, physical, and nuclear properties of uranium hexafluoride as they influence its transport, storage, and the design and operation of plant-scale facilities for production, processing, and conversion to oxide. The papers demonstrate, in an industry often cited for its excellent safety record, continuing efforts to further improve safety in all areas of handling uranium hexafluoride. Selected papers were processed separately for inclusion in the Energy Science and Technology Database.

Not Available

1991-12-31T23:59:59.000Z

355

High Purity Germanium Gamma-PHA Assay of Uranium in Scrap Cans for 321-M Facility  

SciTech Connect (OSTI)

The Analytical Development Section of SRTC was requested by the Facilities Disposition Division to determine the holdup of enriched uranium in the 321-M facility as part of an overall deactivation project of the facility. This report includes a description of two efficiency calibration configurations and also the results of the assay. A description of the quality control checks is included as well.

Salaymeh, S.R.

2002-03-22T23:59:59.000Z

356

Nuclear reactor fuel structure containing uranium alloy wires embedded in a metallic matrix plate  

DOE Patents [OSTI]

A flat or curved plate structure, to be used as fuel in a nuclear reactor, comprises elongated fissionable wires or strips embedded in a metallic continuous non-fissionable matrix plate. The wires or strips are made predominantly of a malleable uranium alloy, such as uranium silicide, uranium gallide or uranium germanide. The matrix plate is made predominantly of aluminum or an aluminum alloy. The wires or strips are located in a single row at the midsurface of the plate, parallel with one another and with the length dimension of the plate. The wires or strips are separated from each other, and from the surface of the plate, by sufficient thicknesses of matrix material, to provide structural integrity and effective fission product retention, under neutron irradiation. This construction makes it safely feasible to provide a high uranium density, so that the uranium enrichment with uranium 235 may be reduced below about 20%, to deter the reprocessing of the uranium for use in nuclear weapons.

Travelli, A.

1985-10-25T23:59:59.000Z

357

Nuclear reactor fuel structure containing uranium alloy wires embedded in a metallic matrix plate  

SciTech Connect (OSTI)

A flat or curved plate structure, to be used as fuel in a nuclear reactor, comprises elongated fissionable wires or strips embedded in a metallic continuous non-fissionable matrix plate. The wires or strips are made predominantly of a malleable uranium alloy, such as uranium silicide, uranium gallide or uranium germanide. The matrix plate is made predominantly of aluminum or an aluminum alloy. The wires or strips are located in a single row at the midsurface of the plate, parallel with one another and with the length dimension of the plate. The wires or strips are separated from each other, and from the surface of the plate, by sufficient thicknesses of matrix material, to provide structural integrity and effective fission product retention, under neutron irradiation. This construction makes it safely feasible to provide a high uranium density, so that the uranium enrichment with uranium 235 may be reduced below about 20%, to deter the reprocessing of the uranium for use in nuclear weapons.

Travelli, Armando (Hinsdale, IL)

1988-01-01T23:59:59.000Z

358

Fuel development activities of the US RERTR Program. [Reduced Enrichment Research and Test Reactor  

SciTech Connect (OSTI)

Progress in the development and irradiation testing of high-density fuels for use with low-enriched uranium in research and test reactors is reported. Swelling and blister-threshold temperature data obtained from the examination of miniature fuel plates containing UAl/sub x/, U/sub 3/O/sub 8/, U/sub 3/Si/sub 2/, or U/sub 3/Si dispersed in an aluminum matrix are presented. Combined with the results of metallurgical examinations, these data show that these four fuel types will perform adequately to full burnup of the /sup 235/U contained in the low-enriched fuel. The exothermic reaction of the uranium-silicide fuels with aluminum has been found to occur at about the same temperature as the melting of the aluminum matrix and cladding and to be essentially quenched by the melting endotherm. A new series of miniature fuel plate irradiations is also discussed.

Snelgrove, J.L.; Domagala, R.F.; Wiencek, T.C.; Copeland, G.L.

1983-01-01T23:59:59.000Z

359

Uranium immobilization and nuclear waste  

SciTech Connect (OSTI)

Considerable information useful in nuclear waste storage can be gained by studying the conditions of uranium ore deposit formation. Further information can be gained by comparing the chemistry of uranium to nuclear fission products and other radionuclides of concern to nuclear waste disposal. Redox state appears to be the most important variable in controlling uranium solubility, especially at near neutral pH, which is characteristic of most ground water. This is probably also true of neptunium, plutonium, and technetium. Further, redox conditions that immobilize uranium should immobilize these elements. The mechanisms that have produced uranium ore bodies in the Earth's crust are somewhat less clear. At the temperatures of hydrothermal uranium deposits, equilibrium models are probably adequate, aqueous uranium (VI) being reduced and precipitated by interaction with ferrous-iron-bearing oxides and silicates. In lower temperature roll-type uranium deposits, overall equilibrium may not have been achieved. The involvement of sulfate-reducing bacteria in ore-body formation has been postulated, but is uncertain. Reduced sulfur species do, however, appear to be involved in much of the low temperature uranium precipitation. Assessment of the possibility of uranium transport in natural ground water is complicated because the system is generally not in overall equilibrium. For this reason, Eh measurements are of limited value. If a ground water is to be capable of reducing uranium, it must contain ions capable of reducing uranium both thermodynamically and kinetically. At present, the best candidates are reduced sulfur species.

Duffy, C.J.; Ogard, A.E.

1982-02-01T23:59:59.000Z

360

Safeguards Verification Measurements using Laser Ablation, Absorbance Ratio Spectrometry in Gaseous Centrifuge Enrichment Plants  

SciTech Connect (OSTI)

Laser Ablation Absorbance Ratio Spectrometry (LAARS) is a new verification measurement technology under development at the US Department of Energy’s (DOE) Pacific Northwest National Laboratory (PNNL). LAARS uses three lasers to ablate and then measure the relative isotopic abundance of uranium compounds. An ablation laser is tightly focused on uranium-bearing solids producing a small plume containing uranium atoms. Two collinear wavelength-tuned spectrometry lasers transit through the plume and the absorbance of U-235 and U-238 isotopes are measured to determine U-235 enrichment. The measurement has high relative precision and detection limits approaching the femtogram range for uranium. It is independent of chemical form and degree of dilution with nuisance dust and other materials. High speed sample scanning and pinpoint characterization allow measurements on millions of particles/hour to detect and analyze the enrichment of trace uranium in samples. The spectrometer is assembled using commercially available components at comparatively low cost, and features a compact and low power design. Future designs can be engineered for reliable, autonomous deployment within an industrial plant environment. Two specific applications of the spectrometer are under development: 1) automated unattended aerosol sampling and analysis and 2) on-site small sample destructive assay measurement. The two applications propose game-changing technological advances in gaseous centrifuge enrichment plant (GCEP) safeguards verification. The aerosol measurement instrument, LAARS-environmental sampling (ES), collects aerosol particles from the plant environment in a purpose-built rotating drum impactor and then uses LAARS-ES to quickly scan the surface of the impactor to measure the enrichments of the captured particles. The current approach to plant misuse detection involves swipe sampling and offsite analysis. Though this approach is very robust it generally requires several months to obtain results from a given sample collection. The destructive assay instrument, LAARS-destructive assay (DA), uses a simple purpose-built fixture with a sampling planchet to collect adsorbed UF6 gas from a cylinder valve or from a process line tap or pigtail. A portable LAARS-DA instrument scans the microgram quantity of uranium collected on the planchet and the assay of the uranium is measured to ~0.15% relative precision. Currently, destructive assay samples for bias defect measurements are collected in small sample cylinders for offsite mass spectrometry measurement.

Anheier, Norman C.; Cannon, Bret D.; Qiao, Hong (Amy) [Amy; Phillips, Jon R.

2012-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


361

Decontamination Systems Information and Research Program. Quarterly report, October--December 1993  

SciTech Connect (OSTI)

This report is a summary of the work conducted for the period of October--December 1993 by the West Virginia University for the US DOE Morgantown Energy Technology Center. Research under the program focuses on pertinent technology for hazardous waste clean-up. This report reflects the progress performed on sixteen technical projects encompassed by this program: Systematic assessment of the state of hazardous waste clean-up technologies; Site remediation technologies: (a) Drain-enhanced soil flushing and (b) In situ bio-remediation of organic contaminants; Excavation systems for hazardous waste sites: Dust control methods for in-situ nuclear waste handling; Chemical destruction of polychlorinated biphenyls; Development of organic sensors: Monolayer and multilayer self-assembled films for chemical sensors; Winfield lock and dam remediation; Assessment of technologies for hazardous waste site remediation: Non-treatment technologies and pilot scale test facility implementation; Remediation of hazardous sites with steam reforming; Microbial enrichment for enhancing biodegradation of hazardous organic wastes in soil; Soil decontamination with a packed flotation column; Treatment of volatile organic compounds using biofilters; Use of granular activated carbon columns for the simultaneous removal of organic, heavy metals, and radionuclides; Compact mercuric iodide detector technology development; Evaluation of IR and mass spectrometric techniques for on-site monitoring of volatile organic compounds; and Improved socio-economic assessment of alternative environmental restoration techniques.

Not Available

1994-02-01T23:59:59.000Z

362

Corrosion-resistant uranium  

DOE Patents [OSTI]

The present invention is directed to the protecting of uranium and uranium alloy articles from corrosion by providing the surfaces of the articles with a layer of an ion-plated metal selected from aluminum and zinc to a thickness of at least 60 microinches and then converting at least the outer surface of the ion-plated layer of aluminum or zinc to aluminum chromate or zinc chromate. This conversion of the aluminum or zinc to the chromate form considerably enhances the corrosion resistance of the ion plating so as to effectively protect the coated article from corrosion.

Hovis, V.M. Jr.; Pullen, W.C.; Kollie, T.G.; Bell, R.T.

1981-10-21T23:59:59.000Z

363

Corrosion-resistant uranium  

DOE Patents [OSTI]

The present invention is directed to the protecting of uranium and uranium alloy articles from corrosion by providing the surfaces of the articles with a layer of an ion-plated metal selected from aluminum and zinc to a thickness of at least 60 microinches and then converting at least the outer surface of the ion-plated layer of aluminum or zinc to aluminum chromate or zinc chromate. This conversion of the aluminum or zinc to the chromate form considerably enhances the corrosion resistance of the ion plating so as to effectively protect the coated article from corrosion.

Hovis, Jr., Victor M. (Kingston, TN); Pullen, William C. (Knoxville, TN); Kollie, Thomas G. (Oak Ridge, TN); Bell, Richard T. (Knoxville, TN)

1983-01-01T23:59:59.000Z

364

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium froma. Uranium

365

Foam and gel methods for the decontamination of metallic surfaces  

DOE Patents [OSTI]

Decontamination of nuclear facilities is necessary to reduce the radiation field during normal operations and decommissioning of complex equipment. In this invention, we discuss gel and foam based diphosphonic acid (HEDPA) chemical solutions that are unique in that these solutions can be applied at room temperature; provide protection to the base metal for continued applications of the equipment; and reduce the final waste form production to one step. The HEDPA gels and foams are formulated with benign chemicals, including various solvents, such as ionic liquids and reducing and complexing agents such as hydroxamic acids, and formaldehyde sulfoxylate. Gel and foam based HEDPA processes allow for decontamination of difficult to reach surfaces that are unmanageable with traditional aqueous process methods. Also, the gel and foam components are optimized to maximize the dissolution rate and assist in the chemical transformation of the gel and foam to a stable waste form.

Nunez, Luis; Kaminski, Michael Donald

2007-01-23T23:59:59.000Z

366

Environmental Assessment for decontamination and dismantlement, Pinellas Plant  

SciTech Connect (OSTI)

The US Department of Energy (DOE) has prepared an Environmental Assessment (EA) (DOE/EA-1092) of the proposed decontamination and dismantlement of the Pinellas Plant in Largo, Florida. Under the Decontamination and Dismantlement EA, the DOE proposes to clean up facilities, structures, and utilities; dismantle specific structures; and mitigate or eliminate any environmental impacts associated with the cleanup, dismantlement, and related activities. Related activities include utilization of specific areas by new tenants prior to full-scale cleanup. Based on the analyses in the EA, the DOE has determined that the proposed action is not a major Federal action significantly affecting the quality of the human environment, within the meaning of the National Environmental Policy Act of 1969. Therefore, the preparation of an environmental impact statement is not required. This report contains the Environmental Assessment, as well as the Finding of No Significant Impact (FONSI).

NONE

1995-06-01T23:59:59.000Z

367

High loading uranium fuel plate  

DOE Patents [OSTI]

Two embodiments of a high uranium fuel plate are disclosed which contain a meat comprising structured uranium compound confined between a pair of diffusion bonded ductile metal cladding plates uniformly covering the meat, the meat having a uniform high fuel loading comprising a content of uranium compound greater than about 45 Vol. % at a porosity not greater than about 10 Vol. %. In a first embodiment, the meat is a plurality of parallel wires of uranium compound. In a second embodiment, the meat is a dispersion compact containing uranium compound. The fuel plates are fabricated by a hot isostatic pressing process.

Wiencek, Thomas C. (Bolingbrook, IL); Domagala, Robert F. (Indian Head Park, IL); Thresh, Henry R. (Palos Heights, IL)

1990-01-01T23:59:59.000Z

368

Proceedings: Decommissioning, Decontamination, ALARA, and Worker Safety Workshop  

SciTech Connect (OSTI)

This workshop on decontamination, ALARA, and worker safety was the sixth in a series initiated by EPRI to aid utility personnel in assessing the technologies for decommissioning nuclear power plants. The workshop focused on specific aspects of decommissioning related to the management of worker radiation exposure and safety. The information presented will help individual utilities assess benefits of programs in these areas for their projects, including their potential to reduce decommissioning costs.

None

2000-09-01T23:59:59.000Z

369

Idaho National Engineering and Environmental Laboratory Site Report on the Production and Use of Recycled Uranium  

SciTech Connect (OSTI)

Recent allegations regarding radiation exposure to radionuclides present in recycled uranium sent to the gaseous diffusion plants prompted the Department of Energy to undertake a system-wide study of recycled uranium. Of particular interest, were the flowpaths from site to site operations and facilities in which exposure to plutonium, neptunium and technetium could occur, and to the workers that could receive a significant radiation dose from handling recycled uranium. The Idaho National Engineering and Environmental Laboratory site report is primarily concerned with two locations. Recycled uranium was produced at the Idaho Chemical Processing Plant where highly enriched uranium was recovered from spent fuel. The other facility is the Specific Manufacturing Facility (SMC) where recycled, depleted uranium is manufactured into shapes for use by their customer. The SMC is a manufacturing facility that uses depleted uranium metal as a raw material that is then rolled and cut into shapes. There are no chemical processes that might concentrate any of the radioactive contaminant species. Recyclable depleted uranium from the SMC facility is sent to a private metallurgical facility for recasting. Analyses on the recast billets indicate that there is no change in the concentrations of transuranics as a result of the recasting process. The Idaho Chemical Processing Plant was built to recover high-enriched uranium from spent nuclear fuel from test reactors. The facility processed diverse types of fuel which required uniquely different fuel dissolution processes. The dissolved fuel was passed through three cycles of solvent extraction which resulted in a concentrated uranyl nitrate product. For the first half of the operating period, the uranium was shipped as the concentrated solution. For the second half of the operating period the uranium solution was thermally converted to granular, uranium trioxide solids. The dose reconstruction project has evaluated work exposure and exposure to the public as the result of normal operations and accidents that occurred at the INEEL. As a result of these studies, the maximum effective dose equivalent from site activities did not exceed seventeen percent of the natural background in Eastern Idaho. There was no year in which the radiation dose to the public exceeded the applicable limits for that year. Worker exposure to recycled uranium was minimized by engineering features that reduced the possibility of direct exposure.

L. C. Lewis; D. C. Barg; C. L. Bendixsen; J. P. Henscheid; D. R. Wenzel; B. L. Denning

2000-09-01T23:59:59.000Z

370

Assessment of strippable coatings for decontamination and decommissioning  

SciTech Connect (OSTI)

Strippable or temporary coatings were developed to assist in the decontamination of the Three Mile Island (TMI-2) reactor. These coatings have become a viable option during the decontamination and decommissioning (D and D) of both US Department of Energy (DOE) and commercial nuclear facilities to remove or fix loose contamination on both vertical and horizontal surfaces. A variety of strippable coatings are available to D and D professionals. However, these products exhibit a wide range of performance criteria and uses. The Hemispheric Center for Environmental Technology (HCET) at Florida International University (FIU) was commissioned to perform a 2-year investigation into strippable coatings. This investigation was divided into four parts: (1) identification of commercially available strippable coating products; (2) survey of D and D professionals to determine current uses of these coatings and performance criteria; (3) design and implementation of a non-radiological testing program to evaluate the physical properties of these coatings; and (4) design and implementation of a radiological testing program to determine decontamination factors and effects of exposure to ionizing radiation. Activities during fiscal year 1997 are described.

Ebadian, M.A.

1998-01-01T23:59:59.000Z

371

FEMO, A FLOW AND ENRICHMENT MONITOR FOR VERIFYING COMPLIANCE WITH INTERNATIONAL SAFEGUARDS REQUIREMENTS AT A GAS CENTRIFUGE ENRICHMENT FACILITY  

SciTech Connect (OSTI)

A number of countries have received construction licenses or are contemplating the construction of large-capacity gas centrifuge enrichment plants (GCEPs). The capability to independently verify nuclear material flows is a key component of international safeguards approaches, and the IAEA does not currently have an approved method to continuously monitor the mass flow of 235U in uranium hexafluoride (UF6) gas streams. Oak Ridge National Laboratory is investigating the development of a flow and enrichment monitor, or FEMO, based on an existing blend-down monitoring system (BDMS). The BDMS was designed to continuously monitor both 235U mass flow and enrichment of UF6 streams at the low pressures similar to those which exists at GCEPs. BDMSs have been installed at three sites-the first unit has operated successfully in an unattended environment for approximately 10 years. To be acceptable to GCEP operators, it is essential that the instrument be installed and maintained without interrupting operations. A means to continuously verify flow as is proposed by FEMO will likely be needed to monitor safeguards at large-capacity plants. This will enable the safeguards effectiveness that currently exists at smaller plants to be maintained at the larger facilities and also has the potential to reduce labor costs associated with inspections at current and future plants. This paper describes the FEMO design requirements, operating capabilities, and development work required before field demonstration.

Gunning, John E [ORNL; Laughter, Mark D [ORNL; March-Leuba, Jose A [ORNL

2008-01-01T23:59:59.000Z

372

Enrichment of light hydrocarbon mixture  

SciTech Connect (OSTI)

Light hydrocarbon enrichment is accomplished using a vertically oriented distillation column having a plurality of vertically oriented, nonselective micro/mesoporous hollow fibers. Vapor having, for example, both propylene and propane is sent upward through the distillation column in between the hollow fibers. Vapor exits neat the top of the column and is condensed to form a liquid phase that is directed back downward through the lumen of the hollow fibers. As vapor continues to ascend and liquid continues to countercurrently descend, the liquid at the bottom of the column becomes enriched in a higher boiling point, light hydrocarbon (propane, for example) and the vapor at the top becomes enriched in a lower boiling point light hydrocarbon (propylene, for example). The hollow fiber becomes wetted with liquid during the process.

Yang; Dali (Los Alamos, NM); Devlin, David (Santa Fe, NM); Barbero, Robert S. (Santa Cruz, NM); Carrera, Martin E. (Naperville, IL); Colling, Craig W. (Warrenville, IL)

2010-08-10T23:59:59.000Z

373

Enrichment of light hydrocarbon mixture  

DOE Patents [OSTI]

Light hydrocarbon enrichment is accomplished using a vertically oriented distillation column having a plurality of vertically oriented, nonselective micro/mesoporous hollow fibers. Vapor having, for example, both propylene and propane is sent upward through the distillation column in between the hollow fibers. Vapor exits neat the top of the column and is condensed to form a liquid phase that is directed back downward through the lumen of the hollow fibers. As vapor continues to ascend and liquid continues to countercurrently descend, the liquid at the bottom of the column becomes enriched in a higher boiling point, light hydrocarbon (propane, for example) and the vapor at the top becomes enriched in a lower boiling point light hydrocarbon (propylene, for example). The hollow fiber becomes wetted with liquid during the process.

Yang, Dali (Los Alamos, NM); Devlin, David (Santa Fe, NM); Barbero, Robert S. (Santa Cruz, NM); Carrera, Martin E. (Naperville, IL); Colling, Craig W. (Warrenville, IL)

2011-11-29T23:59:59.000Z

374

Engineering assessment of inactive uranium mill tailings: Phillips/United Nuclear site, Ambrosia Lake, New Mexico  

SciTech Connect (OSTI)

Ford, Bacon and Davis Utah, Inc., has reevaluated the Phillips/United Nuclear site in order to revise the December 1977 engineering assessment of the problems resulting from the existence of radioactive uranium mill tailings at Ambrosia Lake, New Mexico. This engineering assessment has included the preparation of topographic maps, the performance of core drillings and radiometric measurements sufficient to determine areas and volumes of tailings and radiation exposures of individuals and nearby populations, the investigations of site hydrology and meteorology, and the evaluation and costing of alternative corrective actions. Radon gas released from 2.6 million dry tons of tailings at the Phillips/United Nuclear site constitutes the most significant environmental impact, although windblown tailings and external gamma radiation also are factors. The four alternative actions presented in this engineering assessment range from millsite decontamination with the addition of 3 m of stabilization cover material, to removal of the tailings to remote disposal sites and decontamination of the tailings site. Cost estimates for the four options range from about $21,500,000 for stabilization in-place, to about $45,200,000 for disposal at a distance of about 15 mi. Three principal alternatives for the reprocessing of the Phillips/United Nuclear tailings were examined: heap leaching; treatment at an existing mill; and reprocessing at a new conventional mill constructed for tailings reprocessing.The cost of the uranium recovered would be about $87/lb of U/sub 3/O/sub 8/ by either heap leach or conventional plant process. The spot market price for uranium was $25/lb early in 1981. Reprocessing the Phillips/United Nuclear tailings for uranium recovery does not appear to be economically attractive under present or foreseeable market conditions.

none,

1981-10-01T23:59:59.000Z

375

Engineering assessment of inactive uranium mill tailings: Slick Rock sites, Slick Rock, Colorado  

SciTech Connect (OSTI)

Ford, Bacon and Davis Utah, Inc., has reevaluated the Slick Rock sites in order to revise the October 1977 engineering radioactive uranium mill tailings at Slick Rock, Colorado. This engineering assessment has included the preparation of topographic maps, the performance of core drillings and radiometric measurements sufficient to determine areas and volumes of tailings and radiation exposures of individuals and nearby populations, the investigations of site hydrology and meteorology, and the evaluation and costing of alternative corrective actions. Radon gas released from the 387,000 tons of tailings at the Slick Rock sites constitutes the most significant environmental impact, although windblown tailings and external gamma radiation also are factors. The five alternative actions presented in this engineering assessment include millsite decontamination with the addition of 3 m of stabilization cover material, consolidation of the piles, and removal of the tailings to remote disposal sites and decontamination of the tailings sites. Cost estimates for the five options range from about $6,800,000 for stabilization in-place, to about $11,000,000 for disposal at a distance of about 6.5 mi. Three principal alternatives for the reprocessing of the Slick Rock tailings were examined: heap leaching; treatment at an existing mill; and reprocessing at a new conventional mill constructed for tailings reprocessing. The cost of the uranium recovered would be over $800/lb of U/sub 3/O/sub 8/ whether by conventional or heap leach plant processes. The spot market price for uranium was $25/lb early in 1981. Therefore, reprocessing the tailings for uranium recovery is not economically attractive at present, nor for the foreseeable future.

none,

1981-09-01T23:59:59.000Z

376

Engineering assessment of inactive uranium mill tailings: Maybell Site, Maybell, Colorado  

SciTech Connect (OSTI)

Ford, Bacon and Davis Utah Inc. has reevaluated the Maybell site in order to revise the October 1977 engineering assessment of the problems resulting from the existence of radioactive uranium mill tailings at Maybell, Colorado. This engineering assessment has included the preparation of topographic maps, the performance of core drillings and radiometric measurements sufficient to determine areas and volumes of tailings and radiation exposures of individuals and nearby populations, the investigations of site hydrology and meteorology, and the evaluation and costing of alternative corrective actions. Radon gas released from the 2.6 million dry tons of tailings at the Maybell site constitutes the most significant environmental impact, although windblown tailings and external gamma radiation also are factors. The two alternative actions presented in this engineering assessment range from millsite decontamination with the addition of 3 m of stabilization cover material (Option I), to disposal of the tailings in a nearby open pit mine and decontamination of the tailings site (Option II). Cost estimates for the two options are about $11,700,000 for stabilization in-place and about $22,700,000 for disposal within a distance of 2 mi. Three principal alternatives for the reprocessing of the Maybell tailings were examined: (a) heap leaching; (b) treatment at an existing mill; and (c) reprocessing at a new conventional mill constructed for tailings reprocessing. The cost of the uranium recovered would be about $125 and $165/lb of U/sub 3/O/sub 8/ by heap leach and conventional plant processes, respectively. The spot market price for uranium was $25/lb early in 1981. Therefore, reprocessing the tailings for uranium recovery is not economically attractive at present.

none,

1981-09-01T23:59:59.000Z

377

Standard test methods for chemical, mass spectrometric, spectrochemical, nuclear, and radiochemical analysis of uranium hexafluoride  

E-Print Network [OSTI]

1.1 These test methods cover procedures for subsampling and for chemical, mass spectrometric, spectrochemical, nuclear, and radiochemical analysis of uranium hexafluoride UF6. Most of these test methods are in routine use to determine conformance to UF6 specifications in the Enrichment and Conversion Facilities. 1.2 The analytical procedures in this document appear in the following order: Note 1—Subcommittee C26.05 will confer with C26.02 concerning the renumbered section in Test Methods C761 to determine how concerns with renumbering these sections, as analytical methods are replaced with stand-alone analytical methods, are best addressed in subsequent publications. Sections Subsampling of Uranium Hexafluoride 7 - 10 Gravimetric Determination of Uranium 11 - 19 Titrimetric Determination of Uranium 20 Preparation of High-Purity U3O 8 21 Isotopic Analysis 22 Isotopic Analysis by Double-Standard Mass-Spectrometer Method 23 - 29 Determination of Hydrocarbons, Chlorocarbons, and Partially Substitut...

American Society for Testing and Materials. Philadelphia

2011-01-01T23:59:59.000Z

378

Fabrication of Cerium Oxide and Uranium Oxide Microspheres for Space Nuclear Power Applications  

SciTech Connect (OSTI)

Cerium oxide and uranium oxide microspheres are being produced via an internal gelation sol-gel method to investigate alternative fabrication routes for space nuclear fuels. Depleted uranium and non-radioactive cerium are being utilized as surrogates for plutonium-238 (Pu-238) used in radioisotope thermoelectric generators and for enriched uranium required by nuclear thermal rockets. While current methods used to produce Pu-238 fuels at Los Alamos National Laboratory (LANL) involve the generation of fine powders that pose a respiratory hazard and have a propensity to contaminate glove boxes, the sol-gel route allows for the generation of oxide microsphere fuels through an aqueous route. The sol-gel method does not generate fine powders and may require fewer processing steps than the LANL method with less operator handling. High-quality cerium dioxide microspheres have been fabricated in the desired size range and equipment is being prepared to establish a uranium dioxide microsphere production capability.

Jeffrey A. Katalenich; Michael R. Hartman; Robert C. O'Brien

2013-02-01T23:59:59.000Z

379

From the Lab to the real world : sources of error in UF {sub 6} gas enrichment monitoring  

SciTech Connect (OSTI)

Safeguarding uranium enrichment facilities is a serious concern for the International Atomic Energy Agency (IAEA). Safeguards methods have changed over the years, most recently switching to an improved safeguards model that calls for new technologies to help keep up with the increasing size and complexity of today’s gas centrifuge enrichment plants (GCEPs). One of the primary goals of the IAEA is to detect the production of uranium at levels greater than those an enrichment facility may have declared. In order to accomplish this goal, new enrichment monitors need to be as accurate as possible. This dissertation will look at the Advanced Enrichment Monitor (AEM), a new enrichment monitor designed at Los Alamos National Laboratory. Specifically explored are various factors that could potentially contribute to errors in a final enrichment determination delivered by the AEM. There are many factors that can cause errors in the determination of uranium hexafluoride (UF{sub 6}) gas enrichment, especially during the period when the enrichment is being measured in an operating GCEP. To measure enrichment using the AEM, a passive 186-keV (kiloelectronvolt) measurement is used to determine the {sup 235}U content in the gas, and a transmission measurement or a gas pressure reading is used to determine the total uranium content. A transmission spectrum is generated using an x-ray tube and a “notch” filter. In this dissertation, changes that could occur in the detection efficiency and the transmission errors that could result from variations in pipe-wall thickness will be explored. Additional factors that could contribute to errors in enrichment measurement will also be examined, including changes in the gas pressure, ambient and UF{sub 6} temperature, instrumental errors, and the effects of uranium deposits on the inside of the pipe walls will be considered. The sensitivity of the enrichment calculation to these various parameters will then be evaluated. Previously, UF{sub 6} gas enrichment monitors have required empty pipe measurements to accurately determine the pipe attenuation (the pipe attenuation is typically much larger than the attenuation in the gas). This dissertation reports on a method for determining the thickness of a pipe in a GCEP when obtaining an empty pipe measurement may not be feasible. This dissertation studies each of the components that may add to the final error in the enrichment measurement, and the factors that were taken into account to mitigate these issues are also detailed and tested. The use of an x-ray generator as a transmission source and the attending stability issues are addressed. Both analytical calculations and experimental measurements have been used. For completeness, some real-world analysis results from the URENCO Capenhurst enrichment plant have been included, where the final enrichment error has remained well below 1% for approximately two months.

Lombardi, Marcie L.

2012-03-01T23:59:59.000Z

380

E-Print Network 3.0 - abrasive decontamination operating Sample...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

must be integrated into a program that includes both navigational operation... Venice, Italy 30 September - 3 October 2003 SEDIMENT DECONTAMINATION FOR NAVIGATIONAL AND...

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


381

E-Print Network 3.0 - agricultural pathogen decontamination Sample...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

B. Decontaminate the entire cart (be sure to ... Source: Krovi, Venkat - Department of Mechanical and Aerospace Engineering, State University of New York at Buffalo Collection:...

382

Health care facility-based decontamination of victims exposed to chemical, biological, and radiological materials  

E-Print Network [OSTI]

contaminants, and management of contaminated materials andmanagement, triage, surveillance, decontamination procedures and materials,from the body, and management of contaminated materials and

Koenig, Kristi L MD

2008-01-01T23:59:59.000Z

383

Method of preparation of uranium nitride  

DOE Patents [OSTI]

Method for producing terminal uranium nitride complexes comprising providing a suitable starting material comprising uranium; oxidizing the starting material with a suitable oxidant to produce one or more uranium(IV)-azide complexes; and, sufficiently irradiating the uranium(IV)-azide complexes to produce the terminal uranium nitride complexes.

Kiplinger, Jaqueline Loetsch; Thomson, Robert Kenneth James

2013-07-09T23:59:59.000Z

384

URANIUM MILLING ACTIVITIES AT SEQUOYAH FUELS CORPORATION  

E-Print Network [OSTI]

Sequoyah Fuels Corporation (SFC) describes previous operations at its Gore, Oklahoma, uranium conversion facility as: (1) the recovery of uranium by concentration and purification processes; and (2) the conversion of concentrated and purified uranium ore into uranium hexafluoride (UF 6), or the reduction of depleted uranium tetrafluoride (UF 4) to UF 6. SFC contends that these

unknown authors

385

D0 Decomissioning : Storage of Depleted Uranium Modules Inside D0 Calorimeters after the Termination of D0 Experiment  

SciTech Connect (OSTI)

Dzero liquid Argon calorimeters contain hadronic modules made of depleted uranium plates. After the termination of DO detector's operation, liquid Argon will be transferred back to Argon storage Dewar, and all three calorimeters will be warmed up. At this point, there is no intention to disassemble the calorimeters. The depleted uranium modules will stay inside the cryostats. Depleted uranium is a by-product of the uranium enrichment process. It is slightly radioactive, emits alpha, beta and gamma radiation. External radiation hazards are minimal. Alpha radiation has no external exposure hazards, as dead layers of skin stop it; beta radiation might have effects only when there is a direct contact with skin; and gamma rays are negligible - levels are extremely low. Depleted uranium is a pyrophoric material. Small particles (such as shavings, powder etc.) may ignite with presence of Oxygen (air). Also, in presence of air and moisture it can oxidize. Depleted uranium can absorb moisture and keep oxidizing later, even after air and moisture are excluded. Uranium oxide can powder and flake off. This powder is also pyrographic. Uranium oxide may create health problems if inhaled. Since uranium oxide is water soluble, it may enter the bloodstream and cause toxic effects.

Sarychev, Michael; /Fermilab

2011-09-21T23:59:59.000Z

386

Proceedings of the 1990 International Meeting on Reduced Enrichment for Research and Test Reactors  

SciTech Connect (OSTI)

The global effort to reduce, and possibly, eliminate the international traffic in highly-enriched uranium caused by its use in research reactors requires extensive cooperation and free exchange of information among all participants. To foster this free exchange of information, the Reduced Enrichment Research and Test Reactor (RERTR) Program, at Argonne National Laboratory, sponsored this meeting as the thirteenth of a series which began in 1978. The common effort brought together, past, a large number of specialists from many countries. On hundred twenty-three participants from 26 countries, including scientists, reactor operators, and personnel from commercial fuel suppliers, research centers, and government organizations, convened in Newport, Rhode Island to discuss their results, their activities, and their plans relative to converting research reactors to low-enriched fuels. As more and more reactors convert to the use of low-enriched uranium, the emphasis of our effort has begun to shift from research and development to tasks more directly related to implementation of the new fuels and technologies that have been developed, and to refinements of those fuels and technologies. It is appropriate, for this reason, that the emphasis of this meeting was placed on safety and on conversion experiences. This individual papers in this report have been cataloged separately.

Not Available

1993-07-01T23:59:59.000Z

387

A more accurate and penetrating method to measure the enrichment and mass of UF6 storage containers using passive neutron self-interrogation  

SciTech Connect (OSTI)

This paper describes an unattended mode neutron measurement that can provide the enrichment of the uranium in UF{sub 6} cylinders. The new passive neutron measurement provides better penetration into the uranium mass than prior gamma-ray enrichment measurement methods. The Passive Neutron Enrichment Monitor (PNEM) provides a new measurement technique that uses passive neutron totals and coincidence counting together with neutron self-interrogation to measure the enrichment in the cylinders. The measurement uses the neutron rates from two detector pods. One of the pods has a bare polyethylene surface next to the cylinder and the other polyethylene surface is covered with Cd to prevent thermal neutrons from returning to the cylinder. The primary neutron source from the enriched UF{sub 6} is the alpha-particle decay from the {sub 234}U that interacts with the fluorine to produce random neutrons. The singles neutron counting rate is dominated by the {sub 234}U neutrons with a minor contribution from the induced fissions in the {sub 235}U. However, the doubles counting rate comes primarily from the induced fissions (i.e., multiplication) in the {sub 235}U in enriched uranium. The PNEM concept makes use of the passive neutrons that are initially produced from the {sub 234}U reactions that track the {sub 235}U enrichment during the enrichment process. The induced fission reactions from the thermal-neutron albedo are all from the {sub 235}U and provide a measurement of the {sub 235}U. The Cd ratio has the desirable feature that all of the thermal-neutron-induced fissions in {sub 235}U are independent of the original neutron source. Thus, the ratio is independent of the uranium age, purity, and prior reactor history.

Menlove, Howard O [Los Alamos National Laboratory; Swinhoe, Martyn T [Los Alamos National Laboratory; Miller, Karen A [Los Alamos National Laboratory

2010-01-01T23:59:59.000Z

388

The independent verification process in decommissioning, decontamination, and reutilization activities - description, benefits, and lessons learned  

SciTech Connect (OSTI)

Oak Ridge National Laboratory Environmental Technology Section has been performing Independent Verification (IV) activities for U.S. DOE sites since 1986. DOE has successfully used IV in the Uranium Mill Tailings Remedial Action Program, Decontamination and Decommissioning projects, and Formerly Utilized Sites Remedial Action Projects/Surplus Facilities Management Program. Projects that have undergone IV range from small residential properties to large, industrial sites. The IV process provides a third-party review conducted by an independent organization. The purpose is to verify accuracy and completeness of contractor field measurements and final documentation, evaluate the credibility of procedures, and independently assess post-cleanup conditions versus decommissioning project plans and release criteria. Document reviews of plans, dose models, procedures, and reports are some IV activities undertaken. Independent measurements are also collected during field visits to confirm the contractor`s findings. Corrective actions for discrepancies are suggested if necessary. Finally, archival and reporting of the final site environmental conditions for project closeout and certification are completed. The IV contractor reports to DOE headquarters and acts as a quality assurance feedback mechanism. An IV also provides additional assurance that projects are planned, carried out, and documented properly. Decommissioning projects benefit from the IV process by: (1) cost and time savings from early identification of potential problems, (2) assurance that cleanup meets regulatory guidelines, and (3) technical reviews and consultation with experts in field instrumentation, sampling strategy, etc. Some lessons learned from the IV process include avoiding: (1) improper survey techniques, (2) reporting data in units not comparable with guideline values, (3) premature release of surfaces, (4) poor decommissioning project planning, (5) misapplication of release guidelines. 20 refs.

Egidi, P.V.

1997-06-01T23:59:59.000Z

389

Stimulating the In Situ Activity of Geobacter Species to Remove Uranium from the Groundwater of a Uranium-Contaminated Aquifer  

SciTech Connect (OSTI)

The potential for removing uranium from contaminated groundwater by stimulating the in situ activity of dissimilatory metal-reducing microorganisms was evaluated in a uranium-contaminated aquifer located in Rifle, Colo. Acetate (1 to 3 mM) was injected into the subsurface over a 3-month period via an injection gallery composed of 20 injection wells, which was installed upgradient from a series of 15 monitoring wells. U(VI) concentrations decreased in as little as 9 days after acetate injection was initiated, and within 50 days uranium had declined below the prescribed treatment level of 0.18 _M in some of the monitoring wells. Analysis of 16S ribosomal DNA (rDNA) sequences and phospholipid fatty acid profiles demonstrated that the initial loss of uranium from the groundwater was associated with an enrichment of Geobacter species in the treatment zone. Fe(II) in the groundwater also increased during this period, suggesting that U(VI) reduction was coincident with Fe(III) reduction. As the acetate injection continued over 50 days there was a loss of sulfate from the groundwater and an accumulation of sulfide and the composition of the microbial community changed. Organisms with 16S rDNA sequences most closely related to those of sulfate reducers became predominant, and Geobacter species became a minor component of the community. This apparent switch from Fe(III) reduction to sulfate reduction as the terminal electron accepting process for the oxidation of the injected acetate was associated with an increase in uranium concentration in the groundwater. These results demonstrate that in situ bioremediation of uranium-contaminated groundwater is feasible but suggest that the strategy should be optimized to better maintain long-term activity of Geobacter species.

Anderson, R. T.; Vrionis, Helen A.; Ortiz-Bernad, Irene; Resch, Charles T.; Long, Philip E.; Dayvault, R. D.; Karp, Ken; Marutzky, Sammy J.; Metzler, Donald R.; Peacock, Aaron D.; White, David C.; Lowe, Mary; Lovley, Derek R.

2003-10-01T23:59:59.000Z

390

Long-term criticality control in radioactive waste disposal facilities using depleted uranium  

SciTech Connect (OSTI)

Plant photosynthesis has created a unique planetary-wide geochemistry - an oxidizing atmosphere with oxidizing surface waters on a planetary body with chemically reducing conditions near or at some distance below the surface. Uranium is four orders of magnitude more soluble under chemically oxidizing conditions than it is under chemically reducing conditions. Thus, uranium tends to leach from surface rock and disposal sites, move with groundwater, and concentrate where chemically reducing conditions appear. Earth`s geochemistry concentrates uranium and can separate uranium from all other elements except oxygen, hydrogen (in water), and silicon (silicates, etc). Fissile isotopes include {sup 235}U, {sup 233}U, and many higher actinides that eventually decay to one of these two uranium isotopes. The potential for nuclear criticality exists if the precipitated uranium from disposal sites has a significant fissile enrichment, mass, and volume. The earth`s geochemistry suggests that isotopic dilution of fissile materials in waste with {sup 238}U is a preferred strategy to prevent long-term nuclear criticality in and beyond the boundaries of waste disposal facilities because the {sup 238}U does not separate from the fissile uranium isotopes. Geological, laboratory, and theoretical data indicate that the potential for nuclear criticality can be minimized by diluting fissile materials with-{sup 238}U to 1 wt % {sup 235}U equivalent.

Forsberg, C.W.

1997-02-19T23:59:59.000Z

391

Method for fabricating uranium foils and uranium alloy foils  

DOE Patents [OSTI]

A method of producing thin foils of uranium or an alloy. The uranium or alloy is cast as a plate or sheet having a thickness less than about 5 mm and thereafter cold rolled in one or more passes at substantially ambient temperatures until the uranium or alloy thereof is in the shape of a foil having a thickness less than about 1.0 mm. The uranium alloy includes one or more of Zr, Nb, Mo, Cr, Fe, Si, Ni, Cu or Al.

Hofman, Gerard L. (Downers Grove, IL); Meyer, Mitchell K. (Idaho Falls, ID); Knighton, Gaven C. (Moore, ID); Clark, Curtis R. (Idaho Falls, ID)

2006-09-05T23:59:59.000Z

392

Fissile sample worths in the Uranium/Iron Benchmark  

SciTech Connect (OSTI)

One of the long-standing problems from LMFBR critical experiments is the central worth discrepancy, the consistent overprediction of the reactivity associated with introducing a small material sample near the center of an assembly. Reactivity (sample worth) experiments in ZPR-9, assembly 34, the Uranium/Iron Benchmark (U/Fe), were aimed at investigating this discrepancy. U/Fe had a large, single-region core whose neutronics was governed almost entirely by /sup 235/U and iron. The essentially one-dimensional plate unit cell had one 1.6 mm-wide column of 93% enriched uranium (U(93)) near the center, imbedded in about 50 mm of iron and stainless steel. The neutron spectrum was roughly comparable to that of an LMFBR, but the adjoint spectrum was much flatter than an LMFBR's. The worths of four different fissile materials were measured and the worth of U(93) was measured using several different experimental techniques.

Schaefer, R.W.; Bucher, R.G.

1983-01-01T23:59:59.000Z

393

Recovery and Blend-Down Uranium for Beneficial use in Commercial Reactors - 13373  

SciTech Connect (OSTI)

In April 2001 the Department of Energy (DOE) and the Tennessee Valley Authority (TVA) signed an Interagency Agreement to transfer approximately 33 MT of off-specification (off-spec) highly enriched uranium (HEU) from DOE to TVA for conversion to commercial reactor fuel. Since that time additional surplus off-spec HEU material has been added to the program, making the total approximately 46 MT off-spec HEU. The disposition path for approximately half (23 MT) of this 46 MT of surplus HEU material, was down blending through the H-canyon facility at the Savannah River Site (SRS). The HEU is purified through the H-canyon processes, and then blended with natural uranium (NU) to form low enriched uranium (LEU) solution with a 4.95% U-235 isotopic content. This material was then transported to a TVA subcontractor who converted the solution to uranium oxide and then fabricated into commercial light water reactor (LWR) fuel. This fuel is now powering TVA reactors and supplying electricity to approximately 1 million households in the TVA region. There is still in excess of approximately 10 to 14 MT of off-spec HEU throughout the DOE complex or future foreign and domestic research reactor returns that could be recovered and down blended for use in either currently designed light water reactors, ?5% enriched LEU, or be made available for use in subsequent advanced 'fast' reactor fuel designs, ?19% LEU. (authors)

Magoulas, Virginia [Savannah River National Laboratory, Savannah River Site, Aiken, SC 29808 (United States)] [Savannah River National Laboratory, Savannah River Site, Aiken, SC 29808 (United States)

2013-07-01T23:59:59.000Z

394

Method and apparatus for measuring enrichment of UF6  

DOE Patents [OSTI]

A system and method are disclosed for determining the enrichment of .sup.235U in Uranium Hexafluoride (UF6) utilizing synthesized X-rays which are directed at a container test zone containing a sample of UF6. A detector placed behind the container test zone then detects and counts the X-rays which pass through the container and the UF6. In order to determine the portion of the attenuation due to the UF6 gas alone, this count rate may then be compared to a calibration count rate of X-rays passing through a calibration test zone which contains a vacuum, the test zone having experienced substantially similar environmental conditions as the actual test zone. Alternatively, X-rays of two differing energy levels may be alternately directed at the container, where either the container or the UF6 has a high sensitivity to the difference in the energy levels, and the other having a low sensitivity.

Hill, Thomas Roy (Santa Fe, NM); Ianakiev, Kiril Dimitrov (Los Alamos, NM)

2011-06-07T23:59:59.000Z

395

Stimulating the in situ activity of Geobacter species to remove uranium from the groundwater of a uranium-contaminated aquifer  

E-Print Network [OSTI]

The potential for removing uranium from contaminated groundwater by stimulating the in situ activity of dissimilatory metal-reducing microorganisms was evaluated in a uranium-contaminated aquifer located in Rifle, Colo. Acetate (1 to 3 mM) was injected into the subsurface over a 3-month period via an injection gallery composed of 20 injection wells, which was installed upgradient from a series of 15 monitoring wells. U(VI) concentrations decreased in as little as 9 days after acetate injection was initiated, and within 50 days uranium had declined below the prescribed treatment level of 0.18 ?M in some of the monitoring wells. Analysis of 16S ribosomal DNA (rDNA) sequences and phospholipid fatty acid profiles demonstrated that the initial loss of uranium from the groundwater was associated with an enrichment of Geobacter species in the treatment zone. Fe(II) in the groundwater also increased during this period, suggesting that U(VI) reduction was coincident with Fe(III) reduction. As the acetate injection continued over 50 days there was a loss of sulfate from the groundwater and an accumulation of sulfide and the composition of the microbial community changed. Organisms with 16S rDNA sequences most closely related to those of sulfate reducers became predominant,

Robert T. Anderson; Helen A. Vrionis; Irene Ortiz-bernad; Charles T. Resch; Philip E. Long; Richard Dayvault; Ken Karp; Sam Marutzky; Donald R. Metzler; Aaron Peacock; David C. White; Mary Lowe; Derek R. Lovley

2003-01-01T23:59:59.000Z

396

Precipitation-adsorption process for the decontamination of nuclear waste supernates  

DOE Patents [OSTI]

High-level nuclear waste supernate is decontaminated of cesium by precipitation of the cesium and potassium with sodium tetraphenyl boron. Simultaneously, strontium-90 is removed from the waste supernate sorption of insoluble sodium titanate. The waste solution is then filtered to separate the solution decontaminated of cesium and strontium.

Lee, Lien-Mow (North Augusta, SC); Kilpatrick, Lester L. (Aiken, SC)

1984-01-01T23:59:59.000Z

397

Precipitation-adsorption process for the decontamination of nuclear waste supernates  

DOE Patents [OSTI]

High-level nuclear waste supernate is decontaminated of cesium by precipitation of the cesium and potassium with sodium tetraphenyl boron. Simultaneously, strontium-90 is removed from the waste supernate sorption of insoluble sodium titanate. The waste solution is then filtered to separate the solution decontaminated of cesium and strontium.

Lee, L.M.; Kilpatrick, L.L.

1982-05-19T23:59:59.000Z

398

112 STERN ET AL. Decontamination and BeneficialUse of Dredged Materials  

E-Print Network [OSTI]

112 STERN ET AL. Decontamination and BeneficialUse of Dredged Materials E. A. STERN! U. S";.. ABSTRACT: Our group is leading a large-sale demonstration of dredged material decontamination technologies transformation of contaminated dredged material into an environmentally-benign material used in the manufacture

Brookhaven National Laboratory

399

Decontamination of Dredged Material from The Port of New York and New Jersey  

E-Print Network [OSTI]

of the United States and thereby reducing overall energy consumption. The purpose of this paper is to describeDecontamination of Dredged Material from The Port of New York and New Jersey .K.W. Jones Brookhaven copyrightcoveringthispaper. #12;Decontamination of Dredged Material from The Port of New York and New Jersey K. W. Jones

Brookhaven National Laboratory

400

Decontamination of the populated areas contaminated as a result of nuclear accident  

SciTech Connect (OSTI)

Decontamination tests on urban surfaces contaminated by the Chernobyl accident have shown that Chernobyl fallout behaves differently from fallout from nuclear weapons tests and contamination on surfaces in nuclear power plant. The effectiveness of various decontamination compositions for removing Chernobyl fallout from urban surfaces and machinery was determined in a series of laboratory experiments and field trials.

Voronik, N.I.; Shatilo, N.N.; Davydov, Y.P. [Institute of Radioecological Problems, Minsk-Sosny (Belarus)

1996-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "uranium enrichment decontamination" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


401

Unexpected, Stable Form of Uranium Detected | EMSL  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Unexpected, Stable Form of Uranium Detected Unexpected, Stable Form of Uranium Detected Insights on underappreciated reaction could shed light on environmental cleanup options...

402

Determination of the 235U Mass and Enrichment within Small UF6 Cylinders via a Neutron Coincidence Well Counting System  

SciTech Connect (OSTI)

The construction of three new uranium enrichment facilities in the United States has sparked renewed interest in the development and enhancement of methods to determine the enrichment and fissile mass content of UF6 cylinders. We describe the design and examine the expected performance of a UF6 bottle counter developed for the assay of Type 5A cylinders. The counter, as designed and subsequently constructed, is a tall passive neutron well counter with a clam-shell configuration and graphite end plugs operated in fast neutron mode. Factory performance against expectation is described. The relatively high detection efficiency and effectively 4 detection geometry provide a near-ideal measurement configuration, making the UF6 bottle counter a valuable tool for the evaluation of the neutron coincidence approach to UF6 cylinder assay. The impacts of non-uniform filling, voids, enrichment, and mixed enrichments are examined

McElroy, Robert Dennis [ORNL; Croft, Dr. Stephen [Los Alamos National Laboratory (LANL); Young, Brian M [Canberra Industries, Inc., Meriden, CT; Venkataraman, Ram [Canberra Industries, Inc., Meriden, CT

2011-01-01T23:59:59.000Z

403

Conversion of depleted uranium hexafluoride to a solid uranium compound  

DOE Patents [OSTI]

A process for converting UF.sub.6 to a solid uranium compound such as UO.sub.2 and CaF. The UF.sub.6 vapor form is contacted with an aqueous solution of NH.sub.4 OH at a pH greater than 7 to precipitate at least some solid uranium values as a solid leaving an aqueous solution containing NH.sub.4 OH and NH.sub.4 F and remaining uranium values. The solid uranium values are separated from the aqueous solution of NH.sub.4 OH and NH.sub.4 F and remaining uranium values which is then diluted with additional water precipitating more uranium values as a solid leaving trace quantities of uranium in a dilute aqueous solution. The dilute aqueous solution is contacted with an ion-exchange resin to remove substantially all the uranium values from the dilute aqueous solution. The dilute solution being contacted with Ca(OH).sub.2 to precipitate CaF.sub.2 leaving dilute NH.sub.4 OH.

Rothman, Alan B. (Willowbrook, IL); Graczyk, Donald G. (Lemont, IL); Essling, Alice M. (Elmhurst, IL); Horwitz, E. Philip (Naperville, IL)

2001-01-01T23:59:59.000Z

404

Student Science Enrichment Training Program  

SciTech Connect (OSTI)

Funds are requested for the science enrichment training program (emphasis on chemistry and computer science), which will be held at Claflin College during the 1990 and 1991 summers, concomitant with summer school. The thirty participants will include high school students and some college freshmen; the students will come from rural South Carolina schools with limited science and computer facilities. Focus will be on high ability minority students.

Sandhu, S.S.

1990-12-31T23:59:59.000Z

405

Decontamination and decommissioning surveillance and maintenance report for FY 1991  

SciTech Connect (OSTI)

The Decontamination and Decommissioning (D D) Program has three distinct phases: (1) surveillance and maintenance (S M); (2) decontamination and removal of hazardous materials and equipment (which DOE Headquarters in Washington, D.C., calls Phase I of remediation); and (3) decommissioning and ultimate disposal, regulatory compliance monitoring, and property transfer (which DOE Headquarters calls Phase II of remediation). A large part of D D is devoted to S M at each of the sites. Our S M activities, which are performed on facilities awaiting decommissioning, are designed to minimize potential hazards to human health and the environment by: ensuring adequate containment of residual radioactive and hazardous materials; and, providing physical safety and security controls to minimize potential hazards to on-site personnel and the general public. Typically, we classify maintenance activities as either routine or special (major repairs). Routine maintenance includes such activities as painting, cleaning, vegetation control, minor structural repairs, filter changes, and building system(s) checks. Special maintenance includes Occupational Safety and Health Act facility upgrades, roof repairs, and equipment overhaul. Surveillance activities include inspections, radiological measurements, reporting, records maintenance, and security (as required) for controlling and monitoring access to facilities. This report summarizes out FY 1991 S M activities for the Tennessee plant sites, which include the K-25 Site, the Gas Centrifuge facilities, ORNL, and the Y-12 Plant.

Not Available

1991-12-01T23:59:59.000Z

406

2013 Domestic Uranium Production Report  

E-Print Network [OSTI]

Administration (EIA), the statistical and analytical agency within the U.S. Department of Energy. By law, EIA.S. Energy Information Administration | 2013 Domestic Uranium Production Report iii Preface The U.S. Energy://www.eia.doe.gov/glossary/. #12;U.S. Energy Information Administration | 2013 Domestic Uranium Production Report iv Contents

407

Domestic Uranium Production Report  

Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines AboutDecember 2005 (Thousand9, 2015Year109 AppendixCostsDistributedSep-1410. Uranium

408

Domestic Uranium Production Report  

Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines AboutDecember 2005 (Thousand9, 2015Year109 AppendixCostsDistributedSep-1410. Uranium9.

409

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium from U.S.

410

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium from U.S.2.

411

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium from U.S.2.3.

412

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium from U.S.2.3.5.

413

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium from U.S.2.3.5.3.

414

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium from