National Library of Energy BETA

Sample records for low-enriched uranium billets

  1. 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,...

  2. Possibility of nuclear pumped laser experiment using low enriched uranium

    SciTech Connect (OSTI)

    Obara, Toru; Takezawa, Hiroki [Center for Research into Innovative Nuclear Energy Systems Tokyo Institute of Technology 2-12-1-N1-19, Ookayama Meguro-ku, Tokyo 152-8550 (Japan)

    2012-06-06

    Possibility to perform experiments for nuclear pumped laser oscillation by using low enriched uranium is investigated. Kinetic analyses are performed for two types of reactor design, one is using highly enriched uranium and the other is using low enriched uranium. The reactor design is based on the experiment reactor in IPPE. The results show the oscillation of nuclear pumped laser in the case of low enriched uranium reactor is also possible. The use of low enriched uranium in the experiment will make experiment easier.

  3. Measurements of Low-Enriched Uranium Holdup.

    SciTech Connect (OSTI)

    Belian, A. P. (Anthony P.); Reilly, T. D. (T. Douglas); Russo, P. A. (Phyllis A.); Tobin, S. J. (Stephen J.)

    2005-01-01

    A recent effort determined uranium holdup at a large fuel fabrication facility abroad where low enriched ({approx} 3%) uranium (LEU) oxide feeds the pellet manufacturing process. Measurements taken with both high- and low-resolution gamma-ray spectrometry systems include extensive data for the ventilation and vacuum systems. Equipment dimensions and the corresponding holdup deposit masses are large for LEU. Because deposits are infinitely thick to the 186 keV gamma ray in many locations in an LEU environment, measurements of both the 186 and 1001 keV gamma-rays were required, and self-attenuation was significant at 1001 keV in many cases. These wide-dynamic-range measruements used short count times, portable scintillator detectors, and portable MCAs. Because equipment is elevated above floor levels, most measurements were made with detectors mounted on extended telescoping poles. One of the main goals of this effort was to demonstrate and validate methods for measurement and quantitative analysis of LEU holdup using low-resolution detectors and the Generalized Geometry Holdup (GGH) techniques. The current GGH approach is applied elsewhere for holdup measurements of plutonium and high-enriched uranium. The recent experience is directly applicable to holdup measruements at LEU facilities such as the Paducah and Portmouth gaseous diffusion enrichment plants and elsewhere, including LEU sites where D and D is active. This report discusses the measurement methodology, calibration of the measurement equipment, measurement control, analysis of the data, and the global and local assay results including random and systematic uncertainties. It includes field-validation exercises (multiple calibrated systems that perform measruements on the same extended equipment) as well as quantitative validation results obtained on reference materials assembled to emulate the deposits in an extended vacuum line that was also measured by these techniques. The paper examines the differences in assay results between the low-resolution system using the GGH method and the high-resolution system utilizing the commercially available ISOCS analysis method.

  4. Simulation of transportation of low enriched uranium solutions

    SciTech Connect (OSTI)

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

    1996-08-01

    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.

  5. Development of a low enrichment uranium core for the MIT reactor

    E-Print Network [OSTI]

    Newton, Thomas Henderson

    2006-01-01

    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 ...

  6. Engineering analysis of low enriched uranium fuel using improved zirconium hydride cross sections 

    E-Print Network [OSTI]

    Candalino, Robert Wilcox

    2006-10-30

    for the change out of the existing high enriched uranium fuel to this high-burnup, low enriched uranium fuel design. The codes MCNP and Monteburns were utilized for the neutronic analysis while the code PARET was used to determine fuel and cladding temperatures...

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

    E-Print Network [OSTI]

    Plumer, Kevin E. (Kevin Edward)

    2011-01-01

    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 ...

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

    E-Print Network [OSTI]

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

    2008-01-01

    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 monolithic UMo fuel. The design of an optimum LEU core for the ...

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

    E-Print Network [OSTI]

    Chiang, Keng-Yen

    2012-01-01

    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 ...

  10. Active-Interrogation Measurements of Fast Neutrons from Induced Fission in Low-Enriched Uranium

    SciTech Connect (OSTI)

    J. L. Dolan; M. J. Marcath; M. Flaska; S. A. Pozzi; D. L. Chichester; A. Tomanin; P. Peerani

    2014-02-01

    A detection system was designed with MCNPX-PoliMi to measure induced-fission neutrons from U-235 and U-238 using active interrogation. Measurements were then performed with this system at the Joint Research Centre (JRC) in Ispra, Italy on low-enriched uranium samples. Liquid scintillators measured induced fission neutron to characterize the samples in terms of their uranium mass and enrichment. Results are presented to investigate and support the use of organic liquid scintillators with active interrogation techniques to characterize uranium containing materials.

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

    SciTech Connect (OSTI)

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

    2010-10-01

    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.

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

    SciTech Connect (OSTI)

    NONE

    1995-07-05

    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.

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

    SciTech Connect (OSTI)

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

    2012-06-07

    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.

  14. Conversion and standardization of university reactor fuels using low-enrichment uranium - options and costs

    SciTech Connect (OSTI)

    Harris, D.R.; Matos, J.E.; Young, H.H.

    1985-01-01

    The highly-enriched uranium (HEU) fuel used in twenty United States university reactors can be viewed as contributing to the risk of theft or diversion of weapons-useable material. The US Nuclear Regulatory Commission has issued a policy statement expressing its concern and has published a proposed rule on limiting the use of HEU in NRC-licensed non-power reactors. The fuel options, functional impacts, licensing, and scheduling of conversion and standardization of these reactor fuels to use of low-enrichment uranium (LEU) have been assessed. The university reactors span a wide range in form and function, from medium-power intense neutron sources where HEU fuel may be required, to low-power training and research facilities where HEU fuel is unnecessary. Conversion provides an opportunity to standardize university reactor fuels and improve reactor utilization in some cases. The entire program is estimated to cost about $10 million and to last about five years. Planning for conversion and standardization is facilitated by the US Department of Energy. 20 refs., 1 tab.

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

    SciTech Connect (OSTI)

    Busch, R.D. ); O'Dell, R.D. )

    1991-01-01

    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.

  16. Fuel Grading Study on a Low-Enriched Uranium Fuel Design for the High Flux Isotope Reactor

    SciTech Connect (OSTI)

    Ilas, Germina [ORNL; Primm, Trent [ORNL

    2009-11-01

    An engineering design study that would enable the conversion of the High Flux Isotope Reactor (HFIR) from high-enriched uranium to low-enriched uranium fuel is ongoing at Oak Ridge National Laboratory. The computational models used to search for a low-enriched uranium (LEU) fuel design that would meet the requirements for the conversion study, and the recent results obtained with these models during FY 2009, 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 high-enriched uranium fuel core. These studies 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.

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

    SciTech Connect (OSTI)

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

    2010-02-01

    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.

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

    SciTech Connect (OSTI)

    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

    2011-02-01

    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.

  19. Active-Interrogation Measurements of Induced-Fission Neutrons from Low-Enriched Uranium

    SciTech Connect (OSTI)

    J. L. Dolan; M. J. Marcath; M. Flaska; S. A. Pozzi; D. L. Chichester; A. Tomanin; P. Peerani; G. Nebbia

    2012-07-01

    Protection and control of nuclear fuels is paramount for nuclear security and safeguards; therefore, it is important to develop fast and robust controlling mechanisms to ensure the safety of nuclear fuels. Through both passive- and active-interrogation methods we can use fast-neutron detection to perform real-time measurements of fission neutrons for process monitoring. Active interrogation allows us to use different ranges of incident neutron energy to probe for different isotopes of uranium. With fast-neutron detectors, such as organic liquid scintillation detectors, we can detect the induced-fission neutrons and photons and work towards quantifying a sample’s mass and enrichment. Using MCNPX-PoliMi, a system was designed to measure induced-fission neutrons from U-235 and U-238. Measurements were then performed in the summer of 2010 at the Joint Research Centre in Ispra, Italy. Fissions were induced with an associated particle D-T generator and an isotopic Am-Li source. The fission neutrons, as well as neutrons from (n, 2n) and (n, 3n) reactions, were measured with five 5” by 5” EJ-309 organic liquid scintillators. The D-T neutron generator was available as part of a measurement campaign in place by Padova University. The measurement and data-acquisition systems were developed at the University of Michigan utilizing a CAEN V1720 digitizer and pulse-shape discrimination algorithms to differentiate neutron and photon detections. Low-enriched uranium samples of varying mass and enrichment were interrogated. Acquired time-of-flight curves and cross-correlation curves are currently analyzed to draw relationships between detected neutrons and sample mass and enrichment. In the full paper, the promise of active-interrogation measurements and fast-neutron detection will be assessed through the example of this proof-of-concept measurement campaign. Additionally, MCNPX-PoliMi simulation results will be compared to the measured data to validate the MCNPX-PoliMi code when used for active-interrogation simulations.

  20. PREPARING THE HIGH FLUX ISOTOPE REACTOR FOR CONVERSION TO LOW ENRICHED URANIUM FUEL ? RETURN TO 100 MW

    SciTech Connect (OSTI)

    Smith, Kevin Arthur [ORNL; Primm, Trent [ORNL

    2009-01-01

    The feasibility of low-enriched uranium (LEU) fuel as a replacement for the current, high enriched uranium (HEU) fuel for the High Flux Isotope Reactor (HFIR) has been under study since 2006. Reactor performance studies have been completed for conceptual plate designs and show that maintaining reactor performance while converting to LEU fuel requires returning the reactor power to 100 MW from 85 MW. The analyses required to up-rate the reactor power and the methods to perform these analyses are discussed. Comments regarding the regulatory approval process are provided along with a conceptual schedule.

  1. Design Study for a Low-Enriched Uranium Core for the High Flux Isotope Reactor, Annual Report for FY 2008

    SciTech Connect (OSTI)

    Primm, Trent [ORNL; Chandler, David [ORNL; Ilas, Germina [ORNL; Miller, James Henry [ORNL; Sease, John D [ORNL; Jolly, Brian C [ORNL

    2009-03-01

    This report documents progress made during FY 2008 in studies of converting the High Flux Isotope Reactor (HFIR) from highly 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. Scoping experiments with various manufacturing methods for forming the LEU alloy profile are presented.

  2. Two Methods for Converting a Heavy-Water Research Reactor to Use Low-Enriched-Uranium Fuel to Improve Proliferation Resistance After Startup

    E-Print Network [OSTI]

    Kemp, R. Scott

    This article demonstrates the feasibility of converting a heavy-water research reactor from natural to low-enriched uranium in order to slow the production of weapon-usable plutonium, even if the core cannot be physically ...

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

    SciTech Connect (OSTI)

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

    2014-10-30

    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.

  4. 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...

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

    SciTech Connect (OSTI)

    Ilas, Germina [ORNL; Primm, Trent [ORNL

    2011-05-01

    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.

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

    SciTech Connect (OSTI)

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

    2011-05-12

    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.

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

    SciTech Connect (OSTI)

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

    2012-03-01

    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.

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

    SciTech Connect (OSTI)

    Primm, Trent; Guida, Tracey

    2010-02-01

    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.

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

    E-Print Network [OSTI]

    McCord, Cameron (Cameron Liam)

    2014-01-01

    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 ...

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

    SciTech Connect (OSTI)

    SCHWINKENDORF, K.N.

    2006-05-12

    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.

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

    SciTech Connect (OSTI)

    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

    2009-01-01

    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.

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

    SciTech Connect (OSTI)

    TOFFER, H.

    2006-07-18

    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.

  13. 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)

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

    2006-02-01

    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.

  14. 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)

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

    1986-06-01

    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.

  15. Nuclear safety analyses and core design calculations to convert the Texas A & M University Nuclear Science Center reactor to low enrichment uranium fuel. Final report

    SciTech Connect (OSTI)

    Parish, T.A.

    1995-03-02

    This project involved performing the nuclear design and safety analyses needed to modify the license issued by the Nuclear Regulatory Commission to allow operation of the Texas A& M University Nuclear Science Center Reactor (NSCR) with a core containing low enrichment uranium (LEU) fuel. The specific type of LEU fuel to be considered was the TRIGA 20-20 fuel produced by General Atomic. Computer codes for the neutronic analyses were provided by Argonne National Laboratory (ANL) and the assistance of William Woodruff of ANL in helping the NSCR staff to learn the proper use of the codes is gratefully acknowledged. The codes applied in the LEU analyses were WIMSd4/m, DIF3D, NCTRIGA and PARET. These codes allowed full three dimensional, temperature and burnup dependent calculations modelling the NSCR core to be performed for the first time. In addition, temperature coefficients of reactivity and pulsing calculations were carried out in-house, whereas in the past this modelling had been performed at General Atomic. In order to benchmark the newly acquired codes, modelling of the current NSCR core with highly enriched uranium fuel was also carried out. Calculated results were compared to both earlier licensing calculations and experimental data and the new methods were found to achieve excellent agreement with both. Therefore, even if an LEU core is never loaded at the NSCR, this project has resulted in a significant improvement in the nuclear safety analysis capabilities established and maintained at the NSCR.

  16. 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)

    Rasmussen B.

    2010-01-01

    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.

  17. 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)

    David W. Nigg; Sean R. Morrell

    2012-09-01

    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.

  18. Radionuclide inventories : ORIGEN2.2 isotopic depletion calculation for high burnup low-enriched uranium and weapons-grade mixed-oxide pressurized-water reactor fuel assemblies.

    SciTech Connect (OSTI)

    Gauntt, Randall O.; Ross, Kyle W.; Smith, James Dean; Longmire, Pamela

    2010-04-01

    The Oak Ridge National Laboratory computer code, ORIGEN2.2 (CCC-371, 2002), was used to obtain the elemental composition of irradiated low-enriched uranium (LEU)/mixed-oxide (MOX) pressurized-water reactor fuel assemblies. Described in this report are the input parameters for the ORIGEN2.2 calculations. The rationale for performing the ORIGEN2.2 calculation was to generate inventories to be used to populate MELCOR radionuclide classes. Therefore the ORIGEN2.2 output was subsequently manipulated. The procedures performed in this data reduction process are also described herein. A listing of the ORIGEN2.2 input deck for two-cycle MOX is provided in the appendix. The final output from this data reduction process was three tables containing the radionuclide inventories for LEU/MOX in elemental form. Masses, thermal powers, and activities were reported for each category.

  19. :- : DRILLING URANIUM BILLETS ON A

    Office of Legacy Management (LM)

    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 Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefield Municipal Gas &SCE-SessionsSouth DakotaRobbins and Myers Co -VANaval Ordnance,:n5.5.8 'Xxy";^

  20. EA-1123: Final Environmental Assessment

    Office of Energy Efficiency and Renewable Energy (EERE)

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

  1. EA-1123: Finding of No Significant Impact

    Broader source: Energy.gov [DOE]

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

  2. Process for recovering niobium from uranium-niobium alloys

    DOE Patents [OSTI]

    Wallace, S.A.; Creech, E.T.; Northcutt, W.G.

    1982-09-27

    Niobium is recovered from scrap uranium-niobium alloy by melting the scrap with tin, solidifying the billet thus formed, heating the billet to combine niobium with tin therein, placing the billet in hydrochloric acid to dissolve the uranium and form a precipitate of niobium stannide, then separating the precipitate from the acid.

  3. Process for recovering niobium from uranium-niobium alloys

    DOE Patents [OSTI]

    Wallace, Steven A. (Knoxville, TN); Creech, Edward T. (Oak Ridge, TN); Northcutt, Walter G. (Oak Ridge, TN)

    1983-01-01

    Niobium is recovered from scrap uranium-niobium alloy by melting the scrap with tin, solidifying the billet thus formed, heating the billet to combine niobium with tin therein, placing the billet in hydrochloric acid to dissolve the uranium and leave an insoluble residue of niobium stannide, then separating the niobium stannide from the acid.

  4. Baseline Graphite Characterization: First Billet

    SciTech Connect (OSTI)

    Mark C. Carroll; Joe Lords; David Rohrbaugh

    2010-09-01

    The Next Generation Nuclear Plant Project Graphite Research and Development program is currently establishing the safe operating envelope of graphite core components for a very high temperature reactor design. To meet this goal, the program is generating the extensive amount of quantitative data necessary for predicting the behavior and operating performance of the available nuclear graphite grades. In order determine the in-service behavior of the graphite for the latest proposed designs, two main programs are underway. The first, the Advanced Graphite Creep (AGC) program, is a set of experiments that are designed to evaluate the irradiated properties and behavior of nuclear grade graphite over a large spectrum of temperatures, neutron fluences, and compressive loads. Despite the aggressive experimental matrix that comprises the set of AGC test runs, a limited amount of data can be generated based upon the availability of space within the Advanced Test Reactor and the geometric constraints placed on the AGC specimens that will be inserted. In order to supplement the AGC data set, the Baseline Graphite Characterization program will endeavor to provide supplemental data that will characterize the inherent property variability in nuclear-grade graphite without the testing constraints of the AGC program. This variability in properties is a natural artifact of graphite due to the geologic raw materials that are utilized in its production. This variability will be quantified not only within a single billet of as-produced graphite, but also from billets within a single lot, billets from different lots of the same grade, and across different billets of the numerous grades of nuclear graphite that are presently available. The thorough understanding of this variability will provide added detail to the irradiated property data, and provide a more thorough understanding of the behavior of graphite that will be used in reactor design and licensing. This report covers the development of the Baseline Graphite Characterization program from a testing and data collection standpoint through the completion of characterization on the first billet of nuclear-grade graphite. This data set is the starting point for all future evaluations and comparisons of material properties.

  5. Quadrilateral Cooperation on High-density Low-enriched Uranium...

    National Nuclear Security Administration (NNSA)

    This Site Budget IG Web Policy Privacy No Fear Act Accessibility FOIA Sitemap Federal Government The White House DOE.gov USA.gov Jobs Apply for Our Jobs Our Jobs Working at NNSA...

  6. Billet Heating with the Homopolar Generator 

    E-Print Network [OSTI]

    Weldon, W. F.; Keith, R. E.; Weldon, J. M.

    1980-01-01

    generators, operating in the pulsed mode, offer a fourth possible billet heating method. Although basically a direct resistance heating method, the homopolar generator type of power supply has several advantages over a conventional transformer-type supply...

  7. RELAP5 model of the high flux isotope reactor with low enriched fuel thermal flux profiles

    SciTech Connect (OSTI)

    Banfield, J.; Mervin, B.; Hart, S.; Ritchie, J.; Walker, S.; Ruggles, A.; Maldonado, G. I. [Dept. of Nuclear Engineering, Univ. of Tennessee Knoxville, Knoxville, TN 37996-2300 (United States)

    2012-07-01

    The High Flux Isotope Reactor (HFIR) currently uses highly enriched uranium (HEU) fabricated into involute-shaped fuel plates. It is desired that HFIR be able to use low enriched uranium (LEU) fuel while preserving the current performance capability for its diverse missions in material irradiation studies, isotope production, and the use of neutron beam lines for basic research. Preliminary neutronics and depletion simulations of HFIR with LEU fuel have arrived to feasible fuel loadings that maintain the neutronics performance of the reactor. This article illustrates preliminary models developed for the analysis of the thermal-hydraulic characteristics of the LEU core to ensure safe operation of the reactor. The beginning of life (BOL) LEU thermal flux profile has been modeled in RELAP5 to facilitate steady state simulation of the core cooling, and of anticipated and unanticipated transients. Steady state results are presented to validate the new thermal power profile inputs. A power ramp, slow depressurization at the outlet, and flow coast down transients are also evaluated. (authors)

  8. Method for fabricating .sup.99 Mo production targets using low enriched uranium, .sup.99 Mo production targets comprising low enriched uranium

    DOE Patents [OSTI]

    Wiencek, Thomas C. (Orland Park, IL); Matos, James E. (Oak Park, IL); Hofman, Gerard L. (Downers Grove, IL)

    2000-12-12

    A radioisotope production target and a method for fabricating a radioisotope production target is provided, wherein the target comprises an inner cylinder, a foil of fissionable material circumferentially contacting the outer surface of the inner cylinder, and an outer hollow cylinder adapted to receive the substantially foil-covered inner cylinder and compress tightly against the foil to provide good mechanical contact therewith. The method for fabricating a primary target for the production of fission products comprises preparing a first substrate to receive a foil of fissionable material so as to allow for later removal of the foil from the first substrate, preparing a second substrate to receive the foil so as to allow for later removal of the foil from the second substrate; attaching the first substrate to the second substrate such that the foil is sandwiched between the first substrate and second substrate to prevent foil exposure to ambient atmosphere, and compressing the exposed surfaces of the first and second substrate to assure snug mechanical contact between the foil, the first substrate and the second substrate.

  9. Method for fabricating .sup.99 Mo production targets using low enriched uranium, .sup.99 Mo production targets comprising low enriched uranium

    DOE Patents [OSTI]

    Wiencek, Thomas C. (Orland Park, IL); Matos, James E. (Oak Park, IL); Hofman, Gerard L. (Downers Grove, IL)

    1997-01-01

    A radioisotope production target and a method for fabricating a radioisotope production target is provided, wherein the target comprises an inner cylinder, a foil of fissionable material circumferentially contacting the outer surface of the inner cylinder, and an outer hollow cylinder adapted to receive the substantially foil-covered inner cylinder and compress tightly against the foil to provide good mechanical contact therewith. The method for fabricating a primary target for the production of fission products comprises preparing a first substrate to receive a foil of fissionable material so as to allow for later removal of the foil from the first substrate, preparing a second substrate to receive the foil so as to allow for later removal of the foil from the second substrate; attaching the first substrate to the second substrate such that the foil is sandwiched between the first substrate and second substrate to prevent foil exposure to ambient atmosphere, and compressing the exposed surfaces of the first and second substrate to assure snug mechanical contact between the foil, the first substrate and the second substrate.

  10. Method for fabricating {sup 99}Mo production targets using low enriched uranium, {sup 99}Mo production targets comprising low enriched uranium

    DOE Patents [OSTI]

    Wiencek, T.C.; Matos, J.E.; Hofman, G.L.

    1997-03-25

    A radioisotope production target and a method for fabricating a radioisotope production target is provided, wherein the target comprises an inner cylinder, a foil of fissionable material circumferentially contacting the outer surface of the inner cylinder, and an outer hollow cylinder adapted to receive the substantially foil-covered inner cylinder and compress tightly against the foil to provide good mechanical contact therewith. The method for fabricating a primary target for the production of fission products comprises preparing a first substrate to receive a foil of fissionable material so as to allow for later removal of the foil from the first substrate, preparing a second substrate to receive the foil so as to allow for later removal of the foil from the second substrate; attaching the first substrate to the second substrate such that the foil is sandwiched between the first substrate and second substrate to prevent foil exposure to ambient atmosphere, and compressing the exposed surfaces of the first and second substrate to assure snug mechanical contact between the foil, the first substrate and the second substrate. 3 figs.

  11. Report on the Effect the Low Enriched Uranium Delivered Under the Highly

    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 DeliciousMathematicsEnergyInterestedReplacement-2-A Wholesale Power Rate ScheduleSHERMAN STREET,and S.isEnriched

  12. Quadrilateral Cooperation on High-density Low-enriched Uranium 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity ofkandz-cm11 Outreach Home RoomPreservation of Fe(II) by Carbon-RichProton Delivery and Removal PurchasingProduction: Fact

  13. Method and apparatus for forming billets from metallic chip scraps

    DOE Patents [OSTI]

    Girshov, Vladimir Leonidovich (St. Petersburg, RU); Treschevskiy, Arnold Nikolayevich (St. Petersburg, RU); Kochkin, Victor Georgievich (St. Petersburg, RU); Abramov, Alexey Alexandrovich (St. Petersburg, RU); Sidenko, Natalja Semenovna (St. Petersburg, RU)

    2006-05-02

    After recycled titanium alloy chips are crushed and cleaned, they are pressed into cylindrically briquettes with a relative density of 0.6, and placed into capsules. The capsules are heated and placed into a preheated pressing rig. The pressing rig repetitively applies axial force to the capsule, resulting in a relative density of at least 0.95. The product billets are used for consumable electrodes, secondary casting alloys, forgings, extruded semi-finished products and the like.

  14. Fabrication and Characterization of Uranium-Molybdenum-Zirconium Alloys 

    E-Print Network [OSTI]

    Woolum, Connor

    2014-12-12

    As part of a global effort to convert reactors that require highly enriched uranium to instead operate with low enriched uranium, monolithic fuel plates consisting of a U-Mo fuel meat with a zirconium foil barrier layer and clad in aluminum...

  15. Assuaging Nuclear Energy Risks: The Angarsk International Uranium Enrichment Center

    SciTech Connect (OSTI)

    Myers, Astasia [Stanford University, Stanford, CA 94305, USA and MonAme Scientific Research Center, Ulaanbaatar (Mongolia)

    2011-06-28

    The recent nuclear renaissance has motivated many countries, especially developing nations, to plan and build nuclear power reactors. However, domestic low enriched uranium demands may trigger nations to construct indigenous enrichment facilities, which could be redirected to fabricate high enriched uranium for nuclear weapons. The potential advantages of establishing multinational uranium enrichment sites are numerous including increased low enrichment uranium access with decreased nuclear proliferation risks. While multinational nuclear initiatives have been discussed, Russia is the first nation to actualize this concept with their Angarsk International Uranium Enrichment Center (IUEC). This paper provides an overview of the historical and modern context of the multinational nuclear fuel cycle as well as the evolution of Russia's IUEC, which exemplifies how international fuel cycle cooperation is an alternative to domestic facilities.

  16. India's Worsening Uranium Shortage

    SciTech Connect (OSTI)

    Curtis, Michael M.

    2007-01-15

    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.

  17. The effect of residuals on the presence of intergranular surface cracks on continuously cast billets

    SciTech Connect (OSTI)

    Wijngaarden, M.J.U.T. van; Visagie, G.P.

    1996-12-31

    During 1991, Iscor Vereeniging experienced a dramatic increase in the rejection rate of specialty steel bars rolled from continuously cast billets due to the presence of seams on the bars. The seams originated from tearing of the billets during the first 2 passes in the roughing mill during hot rolling. The defective billets were found to contain fine intergranular cracks on the surface. Such cracks have been described in the literature and have been attributed to the presence of high levels of residuals resulting in the well-known phenomenon of surface hot shortness which results from the enrichment of residuals at the grain boundaries after preferential oxidation of iron during scaling of the steel. The present investigation revealed that the effect of residuals on intergranular surface cracking is a complex interaction between steel composition and casting conditions such as casting speed, intensity of secondary cooling, section size, and mold type. This paper quantifies the effect of residuals on the intergranular surface cracking of continuously cast billets and quantitatively relates the incidence of these cracks to parameters which can be controlled during steelmaking and continuous casting.

  18. Examination of the proposed conversion of the U.S. Navy nuclear fleet from highly enriched Uranium to low enriched Uranium

    E-Print Network [OSTI]

    McCord, Cameron (Cameron Liam)

    2013-01-01

    .The Treaty on the Non-Proliferation of Nuclear Weapons creates a loophole that allows a non-nuclear-weapon country to avoid international safeguards governing fissile materials if it claims that the materials will be used ...

  19. U. S. forms uranium enrichment corporation

    SciTech Connect (OSTI)

    Seltzer, R.

    1993-07-12

    After almost 40 years of operation, the federal government is withdrawing from the uranium enrichment business. On July 1, the Department of Energy turned over to a new government-owned entity--the US Enrichment Corp. (USEC)--both the DOE enrichment plants at Paducah, Ky., and Portsmouth, Ohio, and domestic and international marketing of enriched uranium from them. Pushed by the inability of DOE's enrichment operations to meet foreign competition, Congress established USEC under the National Energy Policy Act of 1992, envisioning the new corporation as the first step to full privatization. With gross revenues of $1.5 billion in fiscal 1992, USEC would rank 275th on the Fortune 500 list of top US companies. USEC will lease from DOE the Paducah and Portsmouth facilities, built in the early 1950s, which use the gaseous diffusion process for uranium enrichment. USEC's stock is held by the US Treasury, to which it will pay annual dividends. Martin Marietta Energy Systems, which has operated Paducah since 1984 and Portsmouth since 1986 for DOE, will continue to operate both plants for USEC. Closing one of the two facilities will be studied, especially in light of a 40% world surplus of capacity over demand. USEC also will consider other nuclear-fuel-related ventures. USEC will produce only low-enriched uranium, not weapons-grade material. Indeed, USEC will implement a contract now being completed under which the US will purchase weapons-grade uranium from dismantled Russian nuclear weapons and convert it into low-enriched uranium for power reactor fuel.

  20. EIS-0240: Disposition of Surplus Highly Enriched Uranium

    Broader source: Energy.gov [DOE]

    The Department proposes to eliminate the proliferation threat of surplus highly enriched uranium (HEU) by blending it down to low enriched uranium (LEU), which is not weapons-usable. The EIS assesses the disposition of a nominal 200 metric tons of surplus HEU. The Preferred Alternative is, where practical, to blend the material for use as LEU and use overtime, in commercial nuclear reactor field to recover its economic value. Material that cannot be economically recovered would be blended to LEU for disposal as low-level radioactive waste.

  1. Status of Uranium Atomic Vapor Laser Isotope Separation Program

    SciTech Connect (OSTI)

    Chen, Hao-Lin; Feinberg, R.M.

    1993-06-01

    This report discusses demonstrations of plant-scale hardware embodying AVLIS technology which were completed in 1992. These demonstrations, designed to provide key economic and technical bases for plant deployment, produced significant quantities of low enriched uranium which could be used for civilian power reactor fuel. We are working with industry to address the integration of AVLIS into the fuel cycle. To prepare for deployment, a conceptual design and cost estimate for a uranium enrichment plant were also completed. The U-AVLIS technology is ready for commercialization.

  2. 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

  3. Safeguarding a NWS International Enrichment Center as an Enriched Uranium Store

    SciTech Connect (OSTI)

    Curtis, Michael M.

    2008-03-31

    The operational and regulatory singularities of a multilateral facility designed to provide enriched uranium to a consortium of members may engender a new sub-category of safeguard criteria for the International Atomic Energy Agency (IAEA). This paper introduces the contingency of monitoring such a facility as a uranium storage center with cylinders containing low-enriched uranium (LEU) as the principal, and perhaps only, material open to verification. Accountancy and verification techniques will be proffered together with disparate means for maintaining continuity of knowledge (CoK) on verified stock.

  4. Design of Complex Systems to Achieve Passive Safety: Natural Circulation Cooling of Liquid Salt Pebble Bed Reactors

    E-Print Network [OSTI]

    Scarlat, Raluca Olga

    2012-01-01

    licensing basis events low enriched uranium liquid metalheat curve for low enriched uranium (LEU) cores. Unlikeclassified as low-enriched uranium. Additionally, while

  5. Long-Term Planning for Nuclear Energy Systems Under Deep Uncertainty

    E-Print Network [OSTI]

    Kim, Lance Kyungwoo

    2011-01-01

    LE and FR strategy Low Enriched Uranium Light Water Reactorhigh throughput of low enriched uranium (LEU) can be readilyreactor consumes low enriched uranium (LEU), generating de-

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

    E-Print Network [OSTI]

    Kim, C K; Park, H D

    2002-01-01

    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...

  7. HIGHLY ENRICHED URANIUM BLEND DOWN PROGRAM AT THE SAVANNAH RIVER SITE PRESENT AND FUTURE

    SciTech Connect (OSTI)

    Magoulas, V; Charles Goergen, C; Ronald Oprea, R

    2008-06-05

    The Department of Energy (DOE) and Tennessee Valley Authority (TVA) entered into an Interagency Agreement to transfer approximately 40 metric tons of highly enriched uranium (HEU) to TVA for conversion to fuel for the Browns Ferry Nuclear Power Plant. Savannah River Site (SRS) inventories included a significant amount of this material, which resulted from processing spent fuel and surplus materials. The HEU is blended with natural uranium (NU) to low enriched uranium (LEU) with a 4.95% 235U isotopic content and shipped as solution to the TVA vendor. The HEU Blend Down Project provided the upgrades needed to achieve the product throughput and purity required and provided loading facilities. The first blending to low enriched uranium (LEU) took place in March 2003 with the initial shipment to the TVA vendor in July 2003. The SRS Shipments have continued on a regular schedule without any major issues for the past 5 years and are due to complete in September 2008. The HEU Blend program is now looking to continue its success by dispositioning an additional approximately 21 MTU of HEU material as part of the SRS Enriched Uranium Disposition Project.

  8. Nonproliferation through delegation

    E-Print Network [OSTI]

    Brown, Robert Louis

    2008-01-01

    to use natural or low enriched uranium (enriched only toenriched to low-enriched or natural uranium. In some cases

  9. Policy Paper 37: Energy and Security in Northeast Asia: Proposals for Nuclear Cooperation

    E-Print Network [OSTI]

    Kaneko, Kumao; Suzuki, Atsuyuki; Choi, Jor-Shan; Fei, Edward

    1998-01-01

    reactors (LWRs) using low-enriched uranium (LEU) as fuelenrichment plant for low-enriched uranium, and a subcritical

  10. Design and Transient Analysis of Passive Safety Cooling Systems for Advanced Nuclear Reactors

    E-Print Network [OSTI]

    Galvez, Cristhian

    2011-01-01

    considers the usage of low enriched uranium fuel. A secondkernels are made from Low Enriched Uranium (LEU) in the form

  11. Development of three-wavelength CCD image pyrometer used for the temperature field measurements of continuous casting billets

    SciTech Connect (OSTI)

    Xie, Zhi; Bai, Haicheng [State Key Laboratory of Synthetical Automation for Process Industries, School of Information Science and Engineering, Northeastern University, Shenyang 110819 (China)] [State Key Laboratory of Synthetical Automation for Process Industries, School of Information Science and Engineering, Northeastern University, Shenyang 110819 (China)

    2014-02-15

    This paper develops an imaging based three-color pyrometer for the monitoring of temperature distribution in a continuous casting billet. A novel optical device, together with an embedded electronic system, is designed to sequentially collect a dark image and three thermal images with specified wavelengths on a same monochromatic charge-coupled-device (CCD). The three thermal images provide the basis for the determination of target temperature, while the dark image is used to online eliminate the dark noise of CCD with a differential method. This image pyrometer is not only independent of target emissivity but also overcomes the dissimilarity of measuring accuracy between the micro-sensors of CCD resulted from the non-uniformity of pixels’ intensity response and the vignetting of optical system. Furthermore, a precise two-color temperature field measuring model on the CCD pyrometer is established, based on which a self-adaptive light-integration mechanism is presented. Compared with the traditional fixed light-integration method, the measuring range of the pyrometer is greatly extended and its sensitivity in low temperature segment is improved. The test results in a steel factory demonstrate that the pyrometer is capable of meeting the requirement of surface temperature measurements about casting billets. Reliability and accuracy of measurement results are also discussed herein.

  12. Uranium industry annual 1997

    SciTech Connect (OSTI)

    NONE

    1998-04-01

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

  13. Report on the Effect the Low Enriched Uranium Delivered Under the Highly Enriched Uranium Agreement Between the Government of the United States and the Government of the Russian Federation has on the

    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 RankADVANCED MANUFACTURINGEnergy BillsNo. 195 - Oct.7, 2015Verizon and VerizonCells: S. DEPARTMENTonReport on

  14. Uranium enrichment

    SciTech Connect (OSTI)

    Not Available

    1991-04-01

    This book presents the GAO's views on the Department of Energy's (DOE) program to develop a new uranium enrichment technology, the atomic vapor laser isotope separation process (AVLIS). Views are drawn from GAO's ongoing review of AVLIS, in which the technical, program, and market issues that need to be addressed before an AVLIS plant is built are examined.

  15. Uranium industry annual 1996

    SciTech Connect (OSTI)

    1997-04-01

    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.

  16. Research Reactor Preparations for the Air Shipment of Highly Enriched Uranium from Romania

    SciTech Connect (OSTI)

    K. J. Allen; I. Bolshinsky; L. L. Biro; M. E. Budu; N. V. Zamfir; M. Dragusin; C. Paunoiu; M. Ciocanescu

    2010-03-01

    In June 2009 two air shipments transported both unirradiated (fresh) and irradiated (spent) Russian-origin highly enriched uranium (HEU) nuclear fuel from two research reactors in Romania to the Russian Federation for conversion to low enriched uranium. The Institute for Nuclear Research at Pitesti (SCN Pitesti) shipped 30.1 kg of HEU fresh fuel pellets to Dimitrovgrad, Russia and the Horia Hulubei National Institute of Physics and Nuclear Engineering (IFIN-HH) shipped 23.7 kilograms of HEU spent fuel assemblies from the VVR S research reactor at Magurele, Romania, to Chelyabinsk, Russia. Both HEU shipments were coordinated by the Russian Research Reactor Fuel Return Program (RRRFR) as part of the U.S. Department of Energy Global Threat Reduction Initiative (GTRI), were managed in Romania by the National Commission for Nuclear Activities Control (CNCAN), and were conducted in cooperation with the Russian Federation State Corporation Rosatom and the International Atomic Energy Agency. Both shipments were transported by truck to and from respective commercial airports in Romania and the Russian Federation and stored at secure nuclear facilities in Russia until the material is converted into low enriched uranium. These shipments resulted in Romania becoming the 3rd country under the RRRFR program and the 14th country under the GTRI program to remove all HEU. This paper describes the research reactor preparations and license approvals that were necessary to safely and securely complete these air shipments of nuclear fuel.

  17. URANIUM IN ALKALINE ROCKS

    E-Print Network [OSTI]

    Murphy, M.

    2011-01-01

    1962. "Diatremes and Uranium Deposits in the Hopi Buttes,H. , 1970. "Low-Grade Uranium Deposits in Agpaitic NephelineL. Torkild, 1974B. "The Uranium Deposit at Kvanefjeld, The

  18. URANIUM IN ALKALINE ROCKS

    E-Print Network [OSTI]

    Murphy, M.

    2011-01-01

    1977. "Geology of Brazil's Uranium and Thorium Occurrences,"A tantalo-niobate of uranium, near pyrochlore. Isometric,niobate and tantalate of uranium, with ferrous iron and rare

  19. Uranium enrichment

    SciTech Connect (OSTI)

    Not Available

    1991-08-01

    This paper reports that in 1990 the Department of Energy began a two-year project to illustrate the technical and economic feasibility of a new uranium enrichment technology-the atomic vapor laser isotope separation (AVLIS) process. GAO believes that completing the AVLIS demonstration project will provide valuable information about the technical viability and cost of building an AVLIS plant and will keep future plant construction options open. However, Congress should be aware that DOE still needs to adequately demonstrate AVLIS with full-scale equipment and develop convincing cost projects. Program activities, such as the plant-licensing process, that must be completed before a plant is built, could take many years. Further, an updated and expanded uranium enrichment analysis will be needed before any decision is made about building an AVLIS plant. GAO, which has long supported legislation that would restructure DOE's uranium enrichment program as a government corporation, encourages DOE's goal of transferring AVLIS to the corporation. This could reduce the government's financial risk and help ensure that the decision to build an AVLIS plant is based on commercial concerns. DOE, however, has no alternative plans should the government corporation not be formed. Further, by curtailing a planned public access program, which would have given private firms an opportunity to learn about the technology during the demonstration project, DOE may limit its ability to transfer AVLIS to the private sector.

  20. Uranium Industry Annual, 1992

    SciTech Connect (OSTI)

    Not Available

    1993-10-28

    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.

  1. Corrosion Evaluation of RERTR Uranium Molybdenum Fuel

    SciTech Connect (OSTI)

    A K Wertsching

    2012-09-01

    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.

  2. Kr Ion Irradiation Study of the Depleted-Uranium Alloys

    SciTech Connect (OSTI)

    J. Gan; D. Keiser; B. Miller; M. Kirk; J. Rest; T. Allen; D. Wachs

    2010-12-01

    Fuel development for the Reduced Enrichment Research and Test Reactor program is tasked with the development of new low-enriched uranium nuclear fuels that can be employed to replace existing highly enriched uranium fuels currently used in some research reactors throughout the world. For dispersion-type fuels, radiation stability of the fuel/cladding interaction product has a strong impact on fuel performance. Three depleted uranium alloys are cast for the radiation stability studies of the fuel/cladding interaction product using Kr ion irradiation to investigate radiation damage from fission products. SEM analysis indicates the presence of the phases of interest: U(Si, Al)3, (U, Mo)(Si, Al)3, UMo2Al20, U6Mo4Al43, and UAl4. Irradiations of TEM disc samples were conducted with 500 keV Kr ions at 200ºC to ion doses up to 2.5 × 1015 ions/cm2 (~ 10 dpa) with an Kr ion flux of 1012 ions/cm2-sec (~ 4.0 × 10-3 dpa/sec). Microstructural evolution of the phases relevant to fuel-cladding interaction products was investigated using transmission electron microscopy.

  3. Method for improving the mechanical properties of uranium-1 to 3 wt % zirconium alloy

    DOE Patents [OSTI]

    Anderson, R.C.

    1983-11-22

    A uranium-1 to 3 wt % zirconium alloy characterized by high strength, high ductility and stable microstructure is fabricated by an improved thermal mechanical process. A homogenous ingot of the alloy which has been reduced in thickness of at least 50% in the two-step forging operation, rolled into a plate with a 75% reduction and then heated in vacuum at a temperature of about 750 to 850/sup 0/C and then quenched in water, is subjected to further thermal-mechanical operation steps to increase the compressive yield strength approximately 30%, stabilize the microstructure, and decrease the variations in mechanical properties throughout the plate is provided. These thermal-mechanical steps are achieved by cold rolling the quenchd plate to reduce the thickness thereof about 8 to 12%, aging the cold rolled plate at a first temperature of about 325 to 375/sup 0/C for five to six hours and then aging the plate at a higher temperature ranging from 480 to 500/sup 0/C for five to six hours prior to cooling the billet to ambient conditions and sizing the billet or plate into articles provides the desired increase in mechanical properties and phase stability throughout the plate.

  4. Overview of transparency issues under the US-Russian highly enriched uranium purchase agreement

    SciTech Connect (OSTI)

    Bieniawski, A.J.; Dougherty, D.R.

    1995-12-31

    The US has signed an Agreement with the Russian Federation for the purchase of 500 metric tons of highly enriched uranium (HEU) derived from dismantled Russian nuclear weapons. The BEU will be blended down to low-enriched uranium (LEU) in Russia and will be transported to the US to be used by fuel Fabricators to make fuel for commercial nuclear power plants. Both the United States and Russia have been preparing to institute transparency measures to provide confidence that the nonproliferation, physical protection, and material control and accounting requirements specified in the Agreement are met. This paper provides a background on the Agreement and subsequent on-going negotiations to develop transparency measures suited to the facilities and processes which are expected to be involved.

  5. Assessment of severe accident source terms in pressurized-water reactors with a 40% mixed-oxide and 60% low-enriched uranium core using MELCOR 1.8.5.

    SciTech Connect (OSTI)

    Gauntt, Randall O.; Goldmann, Andrew S.; Wagner, Kenneth C.; Powers, Dana Auburn; Ashbaugh, Scott G.; Longmire, Pamela

    2010-04-01

    As part of a Nuclear Regulatory Commission (NRC) research program to evaluate the impact of using mixed-oxide (MOX) fuel in commercial nuclear power plants, a study was undertaken to evaluate the impact of the usage of MOX fuel on the consequences of postulated severe accidents. A series of 23 severe accident calculations was performed using MELCOR 1.8.5 for a four-loop Westinghouse reactor with an ice condenser containment. The calculations covered five basic accident classes that were identified as the risk- and consequence-dominant accident sequences in plant-specific probabilistic risk assessments for the McGuire and Catawba nuclear plants, including station blackouts and loss-of-coolant accidents of various sizes, with both early and late containment failures. Ultimately, the results of these MELCOR simulations will be used to provide a supplement to the NRC's alternative source term described in NUREG-1465. Source term magnitude and timing results are presented consistent with the NUREG-1465 format. For each of the severe accident release phases (coolant release, gap release, in-vessel release, ex-vessel release, and late in-vessel release), source term timing information (onset of release and duration) is presented. For all release phases except for the coolant release phase, magnitudes are presented for each of the NUREG-1465 radionuclide groups. MELCOR results showed variation of noble metal releases between those typical of ruthenium (Ru) and those typical of molybdenum (Mo); therefore, results for the noble metals were presented for Ru and Mo separately. The collection of the source term results can be used as the basis to develop a representative source term (across all accident types) that will be the MOX supplement to NUREG-1465.

  6. Method for selective recovery of PET-usable quantities of [.sup.18 F] fluoride and [.sup.13 N] nitrate/nitrite from a single irradiation of low-enriched [.sup.18 O] water

    DOE Patents [OSTI]

    Ferrieri, Richard A. (Patchogue, NY); Schlyer, David J. (Bellport, NY); Shea, Colleen (Wading River, NY)

    1995-06-13

    A process for simultaneously producing PET-usable quantities of [.sup.13 N]NH.sub.3 and [.sup.18 F]F.sup.- for radiotracer synthesis is disclosed. The process includes producing [.sup.13 N]NO.sub.2.sup.- /NO.sub.3.sup.- and [.sup.18 F]F.sup.- simultaneously by exposing a low-enriched (20%-30%) [.sup.18 O]H.sub.2 O target to proton irradiation, sequentially isolating the [.sup.13 N]NO.sub.2.sup.- /NO.sub.3.sup.- and [.sup.18 F]F.sup.- from the [.sup.18 O]H.sub.2 O target, and reducing the [.sup.13 N]NO.sub.2.sup.- /NO.sub.3.sup.- to [.sup.13 N]NH.sub.3. The [.sup.13 N]NH.sub.3 and [.sup.18 F]F.sup.- products are then conveyed to a laboratory for radiotracer applications. The process employs an anion exchange resin for isolation of the isotopes from the [.sup.18 O]H.sub.2 O, and sequential elution of [.sup.13 N]NO.sub.2.sup.- /NO.sub.3.sup.- and [ .sup.18 F]F.sup.- fractions. Also the apparatus is disclosed for simultaneously producing PET-usable quantities of [.sup.13 N]NH.sub.3 and [.sup.18 F]F.sup.- from a single irradiation of a single low-enriched [.sup.18 O]H.sub.2 O target.

  7. Final Uranium Leasing Program Programmatic Environmental Impact...

    Energy Savers [EERE]

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

  8. 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

  9. Method for converting uranium oxides to uranium metal

    DOE Patents [OSTI]

    Duerksen, Walter K. (Norris, TN)

    1988-01-01

    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.

  10. Method of increasing the phase stability and the compressive yield strength of uranium-1 to 3 wt. % zirconium alloy

    DOE Patents [OSTI]

    Anderson, Robert C. (Crossville, TN)

    1986-01-01

    A uranium-1 to 3 wt. % zirconium alloy characterized by high strength, high ductility and stable microstructure is fabricated by an improved thermal mechanical process. A homogenous ingot of the alloy which has been reduced in thickness of at least 50% in the two-step forging operation, rolled into a plate with a 75% reduction and then heated in vacuum at a temperature of about 750.degree. to 850.degree. C. and then quenched in water is subjected to further thermal-mechanical operation steps to increase the compressive yield strength approximately 30%, stabilize the microstructure, and decrease the variations in mechanical properties throughout the plate is provided. These thermal-mechanical steps are achieved by cold rolling the quenched plate to reduce the thickness thereof about 8 to 12%, aging the cold rolled plate at a first temperature of about 325.degree. to 375.degree. C. for five to six hours and then aging the plate at a higher temperature ranging from 480.degree. to 500.degree. C. for five to six hours prior to cooling the billet to ambient conditions and sizing the billet or plate into articles provides the desired increase in mechanical properties and phase stability throughout the plate.

  11. Recovery and Blend-Down Uranium for Beneficial use in Commercial Reactors - 13373

    SciTech Connect (OSTI)

    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)

    2013-07-01

    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)

  12. Compact D-D/D-T neutron generators and their applications

    E-Print Network [OSTI]

    Lou, Tak Pui

    2003-01-01

    HEU research reactors to low enriched uranium by using highPu without U. If low-enriched uranium is used, the gain from

  13. Method for selective recovery of PET-usable quantities of [{sup 18}F] fluoride and [{sup 13}N] nitrate/nitrite from a single irradiation of low-enriched [{sup 18}O] water

    DOE Patents [OSTI]

    Ferrieri, R.A.; Schlyer, D.J.; Shea, C.

    1995-06-13

    A process for simultaneously producing PET-usable quantities of [{sup 13}N]NH{sub 3} and [{sup 18}F]F{sup {minus}} for radiotracer synthesis is disclosed. The process includes producing [{sup 13}N]NO{sub 2}{sup {minus}}/NO{sub 3}{sup {minus}}and [{sup 18}F]F{sup {minus}} simultaneously by exposing a low-enriched (20%-30%) [{sup 18}O]H{sub 2}O target to proton irradiation, sequentially isolating the [{sup 13}N]NO{sub 2}{sup {minus}}/NO{sub 3}{sup {minus}} and [{sup 18}F]F{sup {minus}} from the [{sup 18}O]H{sub 2}O target, and reducing the [{sup 13}N]NO{sub 2}{sup {minus}}/NO{sub 3}{sup {minus}} to [{sup 13}N]NH{sub 3}. The [{sup 13}N]NH{sub 3} and [{sup 18}F]F{sup {minus}} products are then conveyed to a laboratory for radiotracer applications. The process employs an anion exchange resin for isolation of the isotopes from the [{sup 18}O]H{sub 2}O, and sequential elution of [{sup 13}N]NO{sub 2}{sup {minus}}/NO{sub 3}{sup {minus}} and [{sup 18}F]F{sup {minus}} fractions. Also the apparatus is disclosed for simultaneously producing PET-usable quantities of [{sup 13}N]NH{sub 3} and [{sup 18}F]F{sup {minus}} from a single irradiation of a single low-enriched [{sup 18}O]H{sub 2}O target. 2 figs.

  14. Process for continuous production of metallic uranium and uranium alloys

    DOE Patents [OSTI]

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

    1995-06-06

    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.

  15. Process for continuous production of metallic uranium and uranium alloys

    DOE Patents [OSTI]

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

    1995-01-01

    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.

  16. Effect of short-term material balances on the projected uranium measurement uncertainties for the gas centrifuge enrichment plant

    SciTech Connect (OSTI)

    Younkin, J.M.; Rushton, J.E.

    1980-02-05

    A program is under way to design an effective International Atomic Energy Agency (IAEA) safeguards system that could be applied to the Portsmouth Gas Centrifuge Enrichment Plant (GCEP). This system would integrate nuclear material accountability with containment and surveillance. Uncertainties in material balances due to errors in the measurements of the declared uranium streams have been projected on a yearly basis for GCEP under such a system in a previous study. Because of the large uranium flows, the projected balance uncertainties were, in some cases, greater than the IAEA goal quantity of 75 kg of U-235 contained in low-enriched uranium. Therefore, it was decided to investigate the benefits of material balance periods of less than a year in order to improve the sensitivity and timeliness of the nuclear material accountability system. An analysis has been made of projected uranium measurement uncertainties for various short-term material balance periods. To simplify this analysis, only a material balance around the process area is considered and only the major UF/sub 6/ stream measurements are included. That is, storage areas are not considered and uranium waste streams are ignored. It is also assumed that variations in the cascade inventory are negligible compared to other terms in the balance so that the results obtained in this study are independent of the absolute cascade inventory. This study is intended to provide information that will serve as the basis for the future design of a dynamic materials accounting component of the IAEA safeguards system for GCEP.

  17. Preparation of uranium compounds

    DOE Patents [OSTI]

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

    2013-02-19

    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.

  18. Uranium Purchases Report

    Reports and Publications (EIA)

    1996-01-01

    Final issue. This report details natural and enriched uranium purchases as reported by owners and operators of commercial nuclear power plants. 1996 represents the most recent publication year.

  19. U.S.Uranium Reserves

    Gasoline and Diesel Fuel Update (EIA)

    Uranium Reserves Data for: 2003 Release Date: June 2004 Next Release: Not determined Uranium Reserves Estimates The Energy Information Administration (EIA) has reported the...

  20. Uranium dioxide electrolysis

    DOE Patents [OSTI]

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

    2009-12-29

    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.

  1. 2013 Domestic Uranium Production Report

    E-Print Network [OSTI]

    2013 Domestic Uranium Production Report May 2014 Independent Statistics & Analysis www.eia.gov U Administration | 2013 Domestic Uranium Production Report ii Contacts This report was prepared by the staff of the Renewables and Uranium Statistics Team, Office of Electricity, Renewables, and Uranium Statistics. Questions

  2. BEHAVIOR OF METALLIC INCLUSIONS IN URANIUM DIOXIDE

    E-Print Network [OSTI]

    Yang, Rosa L.

    2013-01-01

    Metallic Inclusions in Uranium Dioxide", LBL-11117 (1980).in Hypostoichiornetric Uranium Dioxide 11 , LBL-11095 (OF METALLIC INCLUSIONS IN URANIUM DIOXIDE Rosa L. Yang and

  3. Method for the recovery of uranium values from uranium tetrafluoride

    DOE Patents [OSTI]

    Kreuzmann, Alvin B. (Cincinnati, OH)

    1983-01-01

    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.

  4. Method for the recovery of uranium values from uranium tetrafluoride

    DOE Patents [OSTI]

    Kreuzmann, A.B.

    1982-10-27

    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.

  5. The concept of the use of recycled uranium for increasing the degree of security of export deliveries of fuel for light-water reactors

    SciTech Connect (OSTI)

    Alekseev, P. N.; Ivanov, E. A.; Nevinitsa, V. A.; Ponomarev-Stepnoi, N. N.; Rumyantsev, A. N.; Shmelev, V. M. [Russian Research Center Kurchatov Institute (Russian Federation); Borisevich, V. D.; Smirnov, A. Yu.; Sulaberidze, G. A. [National Nuclear Research University MEPhI (Russian Federation)

    2010-12-15

    The present paper deals with investigation of the possibilities for reducing the risk of proliferation of fissionable materials by means of increasing the degree of protection of fresh fuel intended for light-water reactors against unsanctioned use in the case of withdrawal of a recipient country of deliveries from IAEA safeguards. It is shown that the use of recycled uranium for manufacturing export nuclear fuel makes transfer of nuclear material removed from the fuel assemblies for weapons purposes difficult because of the presence of isotope {sup 232}U, whose content increases when one attempts to enrich uranium extracted from fresh fuel. In combination with restricted access to technologies for isotope separation by means of establishing international centers for uranium enrichment, this technical measure can significantly reduce the risk of proliferation associated with export deliveries of fuel made of low-enriched uranium. The assessment of a maximum level of contamination of nuclear material being transferred by isotope {sup 232}U for the given isotope composition of the initial fuel is obtained. The concept of further investigations of the degree of security of export deliveries of fuel assemblies with recycled uranium intended for light-water reactors is suggested.

  6. file://\\\\fs-f1\\shared\\uranium\\uranium.html

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

    Glossary Home > Nuclear > U.S. Uranium Reserves Estimates U.S. Uranium Reserves Estimates Data for: 2008 Report Released: July 2010 Next Release Date: 2012 Summary The U.S. Energy...

  7. Process for electrolytically preparing uranium metal

    DOE Patents [OSTI]

    Haas, Paul A. (Knoxville, TN)

    1989-01-01

    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.

  8. Long-Term Planning for Nuclear Energy Systems Under Deep Uncertainty

    E-Print Network [OSTI]

    Kim, Lance Kyungwoo

    2011-01-01

    and E. Davies. Uranium Enrichment by Gas Centrifuge. Mills ¢rifuges, capable of producing a high throughput of low enriched uranium (

  9. Uranium-titanium-niobium alloy

    DOE Patents [OSTI]

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

    1990-01-01

    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.

  10. Uranium hexafluoride handling. Proceedings

    SciTech Connect (OSTI)

    Not Available

    1991-12-31

    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.

  11. Corrosion-resistant uranium

    DOE Patents [OSTI]

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

    1981-10-21

    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.

  12. Uranium Transport Modeling

    SciTech Connect (OSTI)

    Bostick, William D.

    2008-01-15

    Uranium contamination is prevalent at many of the U.S. DOE facilities and at several civilian sites that have supported the nuclear fuel cycle. The potential off-site mobility of uranium depends on the partitioning of uranium between aqueous and solid (soil and sediment) phases. Hexavalent U (as uranyl, UO{sub 2}{sup 2+}) is relatively mobile, forming strong complexes with ubiquitous carbonate ion which renders it appreciably soluble even under mild reducing conditions. In the presence of carbonate, partition of uranyl to ferri-hydrate and select other mineral phases is usually maximum in the near-neutral pH range {approx} 5-8. The surface complexation reaction of uranyl with iron-containing minerals has been used as one means to model subsurface migration, used in conjunction with information on the site water chemistry and hydrology. Partitioning of uranium is often studied by short-term batch 'equilibrium' or long-term soil column testing ; MCLinc has performed both of these methodologies, with selection of method depending upon the requirements of the client or regulatory authority. Speciation of uranium in soil may be determined directly by instrumental techniques (e.g., x-ray photoelectron spectroscopy, XPS; x-ray diffraction, XRD; etc.) or by inference drawn from operational estimates. Often, the technique of choice for evaluating low-level radionuclide partitioning in soils and sediments is the sequential extraction approach. This methodology applies operationally-defined chemical treatments to selectively dissolve specific classes of macro-scale soil or sediment components. These methods recognize that total soil metal inventory is of limited use in understanding bioavailability or metal mobility, and that it is useful to estimate the amount of metal present in different solid-phase forms. Despite some drawbacks, the sequential extraction method can provide a valuable tool to distinguish among trace element fractions of different solubility related to mineral phases. Four case studies are presented: Water and Soil Characterization, Subsurface Stabilization of Uranium and other Toxic Metals, Reductive Precipitation (in situ bioremediation) of Uranium, and Physical Transport of Particle-bound Uranium by Erosion.

  13. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9.3.3. Uranium

  14. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9.3.3. Uranium5.

  15. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9.3.3.b. Uranium

  16. High loading uranium fuel plate

    DOE Patents [OSTI]

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

    1990-01-01

    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.

  17. Air Shipment of Highly Enriched Uranium Spent Nuclear Fuel from Romania

    SciTech Connect (OSTI)

    K. J. Allen; I. Bolshinsky; L. L. Biro; M. E. Budu; N. V. Zamfir; M. Dragusin

    2010-07-01

    Romania safely air shipped 23.7 kilograms of Russian origin highly enriched uranium (HEU) spent nuclear fuel from the VVR S research reactor at Magurele, Romania, to the Russian Federation in June 2009. This was the world’s first air shipment of spent nuclear fuel transported in a Type B(U) cask under existing international laws without special exceptions for the air transport licenses. This shipment was coordinated by the Russian Research Reactor Fuel Return Program (RRRFR), part of the U.S. Department of Energy Global Threat Reduction Initiative (GTRI), in cooperation with the Romania National Commission for Nuclear Activities Control (CNCAN), the Horia Hulubei National Institute of Physics and Nuclear Engineering (IFIN-HH), and the Russian Federation State Corporation Rosatom. The shipment was transported by truck to and from the respective commercial airports in Romania and the Russian Federation and stored at a secure nuclear facility in Russia where it will be converted into low enriched uranium. With this shipment, Romania became the 3rd country under the RRRFR program and the 14th country under the GTRI program to remove all HEU. This paper describes the work, equipment, and approvals that were required to complete this spent fuel air shipment.

  18. Improved Irradiation Performance of Uranium-Molybdenum/Aluminum Dispersion Fuel by Silicon Addition in Aluminum

    SciTech Connect (OSTI)

    Yeon Soo Kim; G. L. Hofman; A. B. Robinson; D. M. Wachs

    2013-10-01

    Uranium-molybdenum fuel particle dispersion in aluminum is a form of fuel under development for conversion of high-power research and test reactors from highly enriched to low-enriched uranium in the U.S. Global Threat Reduction Initiative program (also known as the Reduced Enrichment for Research and Test Reactors program). Extensive irradiation tests have been conducted to find a solution for problems caused by interaction layer growth and pore formation between U-Mo and Al. Adding a small amount of Si (up to [approximately]5 wt%) in the Al matrix was one of the proposed remedies. The effect of silicon addition in the Al matrix was examined using irradiation test results by comparing side-by-side samples with different Si additions. Interaction layer growth was progressively reduced with increasing Si addition to the matrix Al, up to 4.8 wt%. The Si addition also appeared to delay pore formation and growth between the U-Mo and Al.

  19. Extrusion-formed uranium-2.4 wt. % article with decreased linear thermal expansion and method for making the same

    DOE Patents [OSTI]

    Anderson, Robert C. (Crossville, TN); Jones, Jack M. (Oak Ridge, TN); Kollie, Thomas G. (Oak Ridge, TN)

    1982-01-01

    The present invention is directed to the fabrication of an article of uranium-2.4 wt. % niobium alloy in which the linear thermal expansion in the direction transverse to the extrusion direction is less than about 0.98% between 22.degree. C. and 600.degree. C. which corresponds to a value greater than the 1.04% provided by previous extrusion operations over the same temperature range. The article with the improved thermal expansion possesses a yield strength at 0.2% offset of at least 400 MPa, an ultimate tensile strength of 1050 MPa, a compressive yield strength of at least 0.2% offset of at least 675 MPa, and an elongation of at least 25% over 25.4 mm/sec. To provide this article with the improved thermal expansion, the uranium alloy billet is heated to 630.degree. C. and extruded in the alpha phase through a die with a reduction ratio of at least 8.4:1 at a ram speed no greater than 6.8 mm/sec. These critical extrusion parameters provide the article with the desired decrease in the linear thermal expansion while maintaining the selected mechanical properties without encountering crystal disruption in the article.

  20. Controlling uranium reactivity March 18, 2008

    E-Print Network [OSTI]

    Meyer, Karsten

    March 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 research groups have been involved in utilizing the large size and unique reactivity of the uranium atom

  1. Method of preparation of uranium nitride

    DOE Patents [OSTI]

    Kiplinger, Jaqueline Loetsch; Thomson, Robert Kenneth James

    2013-07-09

    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.

  2. Method for fabricating uranium foils and uranium alloy foils

    DOE Patents [OSTI]

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

    2006-09-05

    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.

  3. OXYGEN DIFFUSION IN HYPOSTOICHIOMETRIC URANIUM DIOXIDE

    E-Print Network [OSTI]

    Kim, Kee Chul

    2010-01-01

    IN HYPOSTOICHIOMETRIC URANIUM DIOXIDE Kee Chul Kim Ph.D.727-366; Figure 1. Oxygen-uranium phase-equilibrium _ystem [18]. uranium dioxide powders and 18 0 enriched carbon

  4. Uranium in prehistoric Indian pottery 

    E-Print Network [OSTI]

    Filberth, Ernest William

    1976-01-01

    URANIUM IN PREHISTORIC INDIAN POTTERY A Thesis by ERNEST WILLIAM FILBERTH Submitted to the Graduate College of Texas A&M University in partial fulfillment of the requirement for the degree of MASTER OF SCIENCE December 1976 Major Subject...: Chemistry URANIUM IN PREHISTORIC INDIAN POTTERY A Thesis by ERNEST WILLIAM FILBERTH Approved as to style and content by: (Chairman of Committee) (Head of Department) (Member) (Membe (Member) (Member) December 1976 ABSTRACT Uranium in Prehistoric...

  5. Highly Enriched Uranium Materials Facility

    National Nuclear Security Administration (NNSA)

    Appropriations Subcommittee, is shown some of the technology in the Highly Enriched Uranium Materials Facility by Warehousing and Transportation Operations Manager Byron...

  6. Uranium Enrichment Decontamination and Decommissioning Fund's...

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

    Uranium Enrichment Decontamination and Decommissioning Fund's Fiscal Year 2008 and 2007 Financial Statement Audit, OAS-FS-10-05 Uranium Enrichment Decontamination and...

  7. Uranium Biomineralization By Natural Microbial Phosphatase Activities...

    Office of Scientific and Technical Information (OSTI)

    Technical Report: Uranium Biomineralization By Natural Microbial Phosphatase Activities in the Subsurface Citation Details In-Document Search Title: Uranium Biomineralization By...

  8. Conversion of depleted uranium hexafluoride to a solid uranium compound

    DOE Patents [OSTI]

    Rothman, Alan B. (Willowbrook, IL); Graczyk, Donald G. (Lemont, IL); Essling, Alice M. (Elmhurst, IL); Horwitz, E. Philip (Naperville, IL)

    2001-01-01

    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.

  9. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium purchased by

  10. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium purchased byb.

  11. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium purchased byb.S2.

  12. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium purchased

  13. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium purchasedb.

  14. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium purchasedb.4.

  15. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium purchasedb.4..

  16. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium purchasedb.4..0.

  17. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium

  18. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3. Deliveries of

  19. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3. Deliveries of4.

  20. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3. Deliveries

  1. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3. Deliveries6.

  2. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3. Deliveries6.7.

  3. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.

  4. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9. Foreign

  5. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9. Foreign.

  6. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9. Foreign.0.

  7. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9. Foreign.0.1.

  8. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9.

  9. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9.3. Inventories

  10. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9.3.

  11. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9.3.3.

  12. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9.3.3.b.

  13. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9.3.3.b.8.

  14. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming963 1.969 1.979Coal Consumers inYear JanSalesa. Uranium3.9.3.3.b.8.9.

  15. Domestic Uranium Production Report

    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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration would like submit theCovalentLaboratory |Sector Full reportTown2008 Final May1. U.S. uranium

  16. Special Training Materials | Y-12 National Security Complex

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

    Uranium in many forms (metal, oxides) and enrichments (highly enriched uranium, low enriched uranium, natural and depleted) Cesium-137 Cobalt-60 Strontium-90 Others as needed...

  17. EIS-0471: Final Environmental Impact Statement | Department of...

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

    EIS-0468: Final Environmental Impact Statement EA-1607: Final Environmental Assessment Disposition of DOE Excess Depleted Uranium, Natural Uranium, and Low-Enriched Uranium...

  18. APPENDIX J Partition Coefficients For Uranium

    E-Print Network [OSTI]

    APPENDIX J Partition Coefficients For Uranium #12;Appendix J Partition Coefficients For Uranium J.1.0 Background The review of uranium Kd values obtained for a number of soils, crushed rock and their effects on uranium adsorption on soils are discussed below. The solution pH was also used as the basis

  19. SHEEP MOUNTAIN URANIUM PROJECT CROOKS GAP, WYOMING

    E-Print Network [OSTI]

    SHEEP MOUNTAIN URANIUM PROJECT CROOKS GAP, WYOMING US EPA Project Meeting April 7 2011April 7, 2011/Titan Uranium, VP Development · Deborah LebowAal/EPA Region 8 Air Program Introduction to Titan Uranium USA;PROJECT OVERVIEW ·Site Location·Site Location ·Fremont , Wyoming ·Existing Uranium Mine Permit 381C

  20. statistical physics canonical ensemble Uranium Centrifuges

    E-Print Network [OSTI]

    statistical physics canonical ensemble Uranium Centrifuges The easiest type of nuclear weapon of the physics behind crude uranium enrichment methods. 2 The centrifuge concept is a very generic way of trying the uranium, we remove gas from the ends of the centrifuge, where the heavier uranium atoms are more

  1. US-Russian collaboration for enhancing nuclear materials protection, control, and accounting at the Elektrostal uranium fuel-fabrication plant

    SciTech Connect (OSTI)

    Smith, H. [Los Alamos National Lab., NM (United States); Allentuck, J. [Brookhaven National Lab., Upton, NY (United States); Barham, M. [Oak Ridge National Lab., TN (United States); Bishop, M. [Sandia National Labs., Albuquerque, NM (United States); Wentz, D. [Lawrence Livermore National Lab., CA (United States); Steele, B.; Bricker, K. [Pacific Northwest National Lab., Richland, WA (United States); Cherry, R. [USDOE, Washington, DC (United States); Snegosky, T. [Dept. of Defense, Washington, DC (United States). Defense Nuclear Agency

    1996-09-01

    In September 1993, an implementing agreement was signed that authorized collaborative projects to enhance Russian national materials control and accounting, physical protection, and regulatory activities, with US assistance funded by the Nunn-Lugar Act. At the first US-Russian technical working group meeting in Moscow in February 1994, it was decided to identify a model facility where materials protection, control, and accounting (MPC and A) and regulatory projects could be carried out using proven technologies and approaches. The low-enriched uranium (LEU or RBMK and VVER) fuel-fabrication process at Elektrostal was selected, and collaborative work began in June 1994. Based on many factors, including initial successes at Elektrostal, the Russians expanded the cooperation by proposing five additional sites for MPC and A development: the Elektrostal medium-enriched uranium (MEU or BN) fuel-fabrication process and additional facilities at Podolsk, Dmitrovgrad, Obninsk, and Mayak. Since that time, multilaboratory teams have been formed to develop and implement MPC and A upgrades at the additional sites, and much new work is underway. This paper summarizes the current status of MPC and A enhancement projects in the LEU fuel-fabrication process and discusses the status of work that addresses similar enhancements in the MEU (BN) fuel processes at Elektrostal, under the recently expanded US-Russian MPC and A cooperation.

  2. Extrusion-formed uranium-2. 4 wt % article with decreased linear thermal expansion and method for making the same. [Patent application

    DOE Patents [OSTI]

    Anderson, R.C.; Jones, J.M.; Kollie, T.G.

    1982-05-24

    The present invention is directed to the fabrication of an article of uranium-2.4 wt % niobium alloy in which the linear thermal expansion in the direction transverse to the extrusion direction is less than about 0.98% between 22 and 600/sup 0/C which corresponds to a value greater than the 1.04% provided by previous extrusion operations over the same temperature range. The article with the improved thermal expansion possesses a yield strength at 0.2% offset of at least 400 MPa, an ultimate tensile strength of 1050 MPa, a compressive yield strength of at least 0.2% offset of at least 675 MPa, and an elongation of at least 25% over 25.4 mm/s. To provide this article with the improved thermal expansion, the uranium alloy billet is heated to 630/sup 0/C and extruded in the alpha phase through a die with a reduction ratio of at least 8.4:1 at a ram speed no greater than 6.8 mm/s. These critical extrusion parameters provide the article with a desired decrease in the linear thermal expansion while maintaining the selected mechanical properties without encountering crystal disruption in the article.

  3. The End of Cheap Uranium

    E-Print Network [OSTI]

    Michael Dittmar

    2011-06-21

    Historic data from many countries demonstrate that on average no more than 50-70% of the uranium in a deposit could be mined. An analysis of more recent data from Canada and Australia leads to a mining model with an average deposit extraction lifetime of 10+- 2 years. This simple model provides an accurate description of the extractable amount of uranium for the recent mining operations. Using this model for all larger existing and planned uranium mines up to 2030, a global uranium mining peak of at most 58 +- 4 ktons around the year 2015 is obtained. Thereafter we predict that uranium mine production will decline to at most 54 +- 5 ktons by 2025 and, with the decline steepening, to at most 41 +- 5 ktons around 2030. This amount will not be sufficient to fuel the existing and planned nuclear power plants during the next 10-20 years. In fact, we find that it will be difficult to avoid supply shortages even under a slow 1%/year worldwide nuclear energy phase-out scenario up to 2025. We thus suggest that a worldwide nuclear energy phase-out is in order. If such a slow global phase-out is not voluntarily effected, the end of the present cheap uranium supply situation will be unavoidable. The result will be that some countries will simply be unable to afford sufficient uranium fuel at that point, which implies involuntary and perhaps chaotic nuclear phase-outs in those countries involving brownouts, blackouts, and worse.

  4. Helium on Venus: Implications for uranium and thorium

    E-Print Network [OSTI]

    Prather, MJ; Mcelroy, MB

    1983-01-01

    Implications for Uranium and Thorium Abstract. Helium isa wide range of uranium and thorium abundances. simi· lar toof crustal uranium and thorium. Studies of helium in Earth's

  5. THE THEORY OF URANIUM ENRICHMENT BY THE GAS CENTRIFUGE

    E-Print Network [OSTI]

    Olander, Donald R.

    2013-01-01

    Soubbaramayer, (1979) in "Uranium Enrichment", S. Villani,and Davies, E. (1973) "Uranium Enrichment by Gas Centrifuge"Nuclear Energy THE THEORY OF URANIUM ENRICHMENT BY THE GAS

  6. Excess Uranium Inventory Management Plan | Department of Energy

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

    Excess Uranium Inventory Management Plan Excess Uranium Inventory Management Plan The 2013 Excess Uranium Inventory Management Plan describes a framework for the effective...

  7. THE HIGH TEMPERATURE BEHAVIOR OF METALLIC INCLUSIONS IN URANIUM DIOXIDE.

    E-Print Network [OSTI]

    Yang, Rosa Lu.

    2010-01-01

    Products in Irradiated Uranium Dioxide," UKAEA Report AERE-OF METALLIC INCLUSIONS IN URANIUM DIOXIDE Rosa Lu Yang (Chemical State of Irradiated Uranium- Plutonium Oxide Fuel

  8. Uranium hexafluoride bibliography

    SciTech Connect (OSTI)

    Burnham, S.L.

    1988-01-01

    This bibliography is a compilation of reports written about the transportation, handling, safety, and processing of uranium hexafluoride. An on-line literature search was executed using the DOE Energy files and the Nuclear Science Abstracts file to identify pertinent reports. The DOE Energy files contain unclassified information that is processed at the Office of Scientific and Technical Information of the US Department of Energy. The reports selected from these files were published between 1974 and 1983. Nuclear Science Abstracts contains unclassified international nuclear science and technology literature published from 1948 to 1976. In addition, scientific and technical reports published by the US Atomic Energy Commission and the US Energy Research and Development Administration, as well as those published by other agencies, universities, and industrial and research organizations, are included in the Nuclear Science Abstracts file. An alphabetical listing of the acronyms used to denote the corporate sponsors follows the bibliography.

  9. 2014 Uranium Marketing Annual Report

    U.S. Energy Information Administration (EIA) 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| Open Energy Informationmonthly gasoline price to fall toUranium Marketing Annual Report 2014 Uranium 201457 201425.

  10. 2014 Uranium Marketing Annual Report

    U.S. Energy Information Administration (EIA) 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| Open Energy Informationmonthly gasoline price to fall toUranium Marketing Annual Report 2014 Uranium 201457

  11. 2014 Uranium Marketing Annual Report

    U.S. Energy Information Administration (EIA) 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| Open Energy Informationmonthly gasoline price to fall toUranium Marketing Annual Report 2014 Uranium 201457Feed

  12. 2014 Uranium Marketing Annual Report

    U.S. Energy Information Administration (EIA) 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| Open Energy Informationmonthly gasoline price to fall toUranium Marketing Annual Report 2014 Uranium

  13. 2014 Uranium Marketing Annual Report

    U.S. Energy Information Administration (EIA) 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| Open Energy Informationmonthly gasoline price to fall toUranium Marketing Annual Report 2014 Uranium17. Purchases of

  14. 2014 Uranium Marketing Annual Report

    U.S. Energy Information Administration (EIA) 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| Open Energy Informationmonthly gasoline price to fall toUranium Marketing Annual Report 2014 Uranium17. Purchases

  15. 2014 Uranium Marketing Annual Report

    U.S. Energy Information Administration (EIA) 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| Open Energy Informationmonthly gasoline price to fall toUranium Marketing Annual Report 2014 Uranium17.

  16. 2014 Uranium Marketing Annual Report

    U.S. Energy Information Administration (EIA) 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| Open Energy Informationmonthly gasoline price to fall toUranium Marketing Annual Report 20144. Uranium sellers to

  17. 2014 Uranium Marketing Annual Survey

    U.S. Energy Information Administration (EIA) 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| Open Energy Informationmonthly gasoline price to fall toUranium Marketing Annual Report 20144. Uranium sellers to57.

  18. Laser induced phosphorescence uranium analysis

    DOE Patents [OSTI]

    Bushaw, Bruce A. (Kennewick, WA)

    1986-01-01

    A method is described for measuring the uranium content of aqueous solutions wherein a uranyl phosphate complex is irradiated with a 5 nanosecond pulse of 425 nanometer laser light and resultant 520 nanometer emissions are observed for a period of 50 to 400 microseconds after the pulse. Plotting the natural logarithm of emission intensity as a function of time yields an intercept value which is proportional to uranium concentration.

  19. Laser induced phosphorescence uranium analysis

    DOE Patents [OSTI]

    Bushaw, B.A.

    1983-06-10

    A method is described for measuring the uranium content of aqueous solutions wherein a uranyl phosphate complex is irradiated with a 5 nanosecond pulse of 425 nanometer laser light and resultant 520 nanometer emissions are observed for a period of 50 to 400 microseconds after the pulse. Plotting the natural logarithm of emission intensity as a function of time yields an intercept value which is proportional to uranium concentration.

  20. Beneficial Uses of Depleted Uranium

    SciTech Connect (OSTI)

    Brown, C. [U.S. Department of Energy, Germantown, MD (United States); Croff, A.G.; Haire, M. J. [Oak Ridge National Lab., TN (United States)

    1997-08-01

    Naturally occurring uranium contains 0.71 wt% {sup 235}U. In order for the uranium to be useful in most fission reactors, it must be enriched the concentration of the fissile isotope {sup 235}U must be increased. Depleted uranium (DU) is a co-product of the processing of natural uranium to produce enriched uranium, and DU has a {sup 235}U concentration of less than 0.71 wt%. In the United States, essentially all of the DU inventory is in the chemical form of uranium hexafluoride (UF{sub 6}) and is stored in large cylinders above ground. If this co-product material were to be declared surplus, converted to a stable oxide form, and disposed, the costs are estimated to be several billion dollars. Only small amounts of DU have at this time been beneficially reused. The U.S. Department of Energy (DOE) has begun the Beneficial Uses of DU Project to identify large-scale uses of DU and encourage its reuse for the primary purpose of potentially reducing the cost and expediting the disposition of the DU inventory. This paper discusses the inventory of DU and its rate of increase; DU disposition options; beneficial use options; a preliminary cost analysis; and major technical, institutional, and regulatory issues to be resolved.

  1. Standard Test Method for Determination of Uranium, Oxygen to Uranium (O/U), and Oxygen to Metal (O/M) in Sintered Uranium Dioxide and Gadolinia-Uranium Dioxide Pellets by Atmospheric Equilibration

    E-Print Network [OSTI]

    American Society for Testing and Materials. Philadelphia

    2007-01-01

    Standard Test Method for Determination of Uranium, Oxygen to Uranium (O/U), and Oxygen to Metal (O/M) in Sintered Uranium Dioxide and Gadolinia-Uranium Dioxide Pellets by Atmospheric Equilibration

  2. Standard practice for removal of uranium or plutonium, or both, for impurity assay in uranium or plutonium materials

    E-Print Network [OSTI]

    American Society for Testing and Materials. Philadelphia

    2006-01-01

    Standard practice for removal of uranium or plutonium, or both, for impurity assay in uranium or plutonium materials

  3. Uranium Tris-aryloxide Derivatives Supported by Triazacyclononane: Engendering a Reactive Uranium(III)

    E-Print Network [OSTI]

    Meyer, Karsten

    Uranium Tris-aryloxide Derivatives Supported by Triazacyclononane: Engendering a Reactive Uranium-mail: kmeyer@ucsd.edu Abstract: The synthesis and spectroscopic characterization of the mononuclear uranium complex [((ArO)3tacn)UIII (NCCH3)] is reported. The uranium(III) complex reacts with organic azides

  4. Inherently safe in situ uranium recovery

    DOE Patents [OSTI]

    Krumhansl, James L; Brady, Patrick V

    2014-04-29

    An in situ recovery of uranium operation involves circulating reactive fluids through an underground uranium deposit. These fluids contain chemicals that dissolve the uranium ore. Uranium is recovered from the fluids after they are pumped back to the surface. Chemicals used to accomplish this include complexing agents that are organic, readily degradable, and/or have a predictable lifetime in an aquifer. Efficiency is increased through development of organic agents targeted to complexing tetravalent uranium rather than hexavalent uranium. The operation provides for in situ immobilization of some oxy-anion pollutants under oxidizing conditions as well as reducing conditions. The operation also artificially reestablishes reducing conditions on the aquifer after uranium recovery is completed. With the ability to have the impacted aquifer reliably remediated, the uranium recovery operation can be considered inherently safe.

  5. The End of Cheap Uranium

    E-Print Network [OSTI]

    Dittmar, Michael

    2011-01-01

    Historic data from many countries demonstrate that on average no more than 50-70% of the uranium in a deposit could be mined. An analysis of more recent data from Canada and Australia leads to a mining model with an average deposit extraction lifetime of 10+- 2 years. This simple model provides an accurate description of the extractable amount of uranium for the recent mining operations. Using this model for all larger existing and planned uranium mines up to 2030, a global uranium mining peak of at most 58 +- 4 ktons around the year 2015 is obtained. Thereafter we predict that uranium mine production will decline to at most 54 +- 5 ktons by 2025 and, with the decline steepening, to at most 41 +- 5 ktons around 2030. This amount will not be sufficient to fuel the existing and planned nuclear power plants during the next 10-20 years. In fact, we find that it will be difficult to avoid supply shortages even under a slow 1%/year worldwide nuclear energy phase-out scenario up to 2025. We thus suggest that a world...

  6. Decolonizing cartographies : sovereignty, territoriality, and maps of meaning in the uranium landscape

    E-Print Network [OSTI]

    Voyles, Traci Brynne

    2010-01-01

    227! Figure 19 Uranium depositsthe Geological Features and Uranium Deposits in the Shiprockresource sovereignty” to uranium deposits located on Native

  7. URANIUM MILL TAILINGS RADON FLUX CALCULATIONS

    E-Print Network [OSTI]

    URANIUM MILL TAILINGS RADON FLUX CALCULATIONS PIÑON RIDGE PROJECT MONTROSE COUNTY, COLORADO (EFRC) proposes to license, construct, and operate a conventional acid leach uranium and vanadium mill storage pad, and access roads. The mill is designed to process ore containing uranium and vanadium

  8. High strength uranium-tungsten alloy process

    DOE Patents [OSTI]

    Dunn, Paul S. (Santa Fe, NM); Sheinberg, Haskell (Los Alamos, NM); Hogan, Billy M. (Los Alamos, NM); Lewis, Homer D. (Bayfield, CO); Dickinson, James M. (Los Alamos, NM)

    1990-01-01

    Alloys of uranium and tungsten and a method for making the alloys. The amount of tungsten present in the alloys is from about 4 wt % to about 35 wt %. Tungsten particles are dispersed throughout the uranium and a small amount of tungsten is dissolved in the uranium.

  9. High strength uranium-tungsten alloys

    DOE Patents [OSTI]

    Dunn, Paul S. (Santa Fe, NM); Sheinberg, Haskell (Los Alamos, NM); Hogan, Billy M. (Los Alamos, NM); Lewis, Homer D. (Bayfield, CO); Dickinson, James M. (Los Alamos, NM)

    1991-01-01

    Alloys of uranium and tungsten and a method for making the alloys. The amount of tungsten present in the alloys is from about 4 wt % to about 35 wt %. Tungsten particles are dispersed throughout the uranium and a small amount of tungsten is dissolved in the uranium.

  10. Y-12 Uranium Exposure Study

    SciTech Connect (OSTI)

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

    1999-08-05

    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.

  11. Continuous reduction of uranium tetrafluoride

    SciTech Connect (OSTI)

    DeMint, A.L.; Maxey, A.W.

    1993-10-21

    Operation of a pilot-scale system for continuous metallothermic reduction of uranium tetrafluoride (UF{sub 4} or green salt) has been initiated. This activity is in support of the development of a cost- effective process to produce uranium-iron (U-Fe) alloy feed for the Uranium-Atomic Vapor Laser Isotope Separation (U-AVLIS) program. To date, five runs have been made to reduce green salt (UF{sub 4}) with magnesium. During this quarter, three runs were made to perfect the feeding system, examine feed rates, and determine the need for a crust breaker/stirrer. No material was drawn off in any of the runs; both product metal and by-product salt were allowed to accumulate in the reactor.

  12. 2014 Uranium Marketing Annual Report

    U.S. Energy Information Administration (EIA) 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| Open Energy Informationmonthly gasoline price to fall toUranium Marketing Annual Report 2014 Uranium 201457 201425.+1

  13. 2014 Uranium Marketing Annual Report

    U.S. Energy Information Administration (EIA) 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| Open Energy Informationmonthly gasoline price to fall toUranium Marketing Annual Report 2014 Uranium17. Purchases6a.

  14. Process for alloying uranium and niobium

    DOE Patents [OSTI]

    Holcombe, Cressie E. (Farragut, TN); Northcutt, Jr., Walter G. (Oak Ridge, TN); Masters, David R. (Knoxville, TN); Chapman, Lloyd R. (Knoxville, TN)

    1991-01-01

    Alloys such as U-6Nb are prepared by forming a stacked sandwich array of uraniun sheets and niobium powder disposed in layers between the sheets, heating the array in a vacuum induction melting furnace to a temperature such as to melt the uranium, holding the resulting mixture at a temperature above the melting point of uranium until the niobium dissolves in the uranium, and casting the uranium-niobium solution. Compositional uniformity in the alloy product is enabled by use of the sandwich structure of uranium sheets and niobium powder.

  15. Domestic utility attitudes toward foreign uranium supply

    SciTech Connect (OSTI)

    Not Available

    1981-06-01

    The current embargo on the enrichment of foreign-origin uranium for use in domestic utilization facilities is scheduled to be removed in 1984. The pending removal of this embargo, complicated by a depressed worldwide market for uranium, has prompted consideration of a new or extended embargo within the US Government. As part of its on-going data collection activities, Nuclear Resources International (NRI) has surveyed 50 domestic utility/utility holding companies (representing 60 lead operator-utilities) on their foreign uranium purchase strategies and intentions. The most recent survey was conducted in early May 1981. A number of qualitative observations were made during the course of the survey. The major observations are: domestic utility views toward foreign uranium purchase are dynamic; all but three utilities had some considered foreign purchase strategy; some utilities have problems with buying foreign uranium from particular countries; an inducement is often required by some utilities to buy foreign uranium; opinions varied among utilities concerning the viability of the domestic uranium industry; and many utilities could have foreign uranium fed through their domestic uranium contracts (indirect purchases). The above observations are expanded in the final section of the report. However, it should be noted that two of the observations are particularly important and should be seriously considered in formulation of foreign uranium import restrictions. These important observations are the dynamic nature of the subject matter and the potentially large and imbalanced effect the indirect purchases could have on utility foreign uranium procurement.

  16. Uranium 2005 resources, production and demand

    E-Print Network [OSTI]

    Organisation for Economic Cooperation and Development. Paris

    2006-01-01

    Published every other year, Uranium Resources, Production, and Demand, or the "Red Book" as it is commonly known, is jointly prepared by the OECD Nuclear Energy Agency and the International Atomic Energy Agency. It is the recognised world reference on uranium and is based on official information received from 43 countries. This 21st edition presents the results of a thorough review of world uranium supplies and demand as of 1st January 2005 and provides a statistical profile of the world uranium industry in the areas of exploration, resource estimates, production and reactor-related requirements. It provides substantial new information from all major uranium production centres in Africa, Australia, Central Asia, Eastern Europe and North America. Projections of nuclear generating capacity and reactor-related uranium requirements through 2025 are provided as well as a discussion of long-term uranium supply and demand issues. This edition focuses on recent price and production increases that could signal major c...

  17. EPA Update: NESHAP Uranium Activities

    E-Print Network [OSTI]

    EPA Update: NESHAP Uranium Activities Reid J. Rosnick Environmental Protection Agency Radiation Mining (Clean Air Act) · 40 CFR 61.20, Subpart B regulations limiting radon emissions from underground air radon standard not to exceed 10 mrem/yr to any member of the public-compliance determined

  18. Uranium isotopes fingerprint biotic reduction

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Stylo, Malgorzata; Neubert, Nadja; Wang, Yuheng; Monga, Nikhil; Romaniello, Stephen J.; Weyer, Stefan; Bernier-Latmani, Rizlan

    2015-04-20

    Knowledge of paleo-redox conditions in the Earth’s history provides a window into events that shaped the evolution of life on our planet. The role of microbial activity in paleo-redox processes remains unexplored due to the inability to discriminate biotic from abiotic redox transformations in the rock record. The ability to deconvolute these two processes would provide a means to identify environmental niches in which microbial activity was prevalent at a specific time in paleo-history and to correlate specific biogeochemical events with the corresponding microbial metabolism. Here, we demonstrate that the isotopic signature associated with microbial reduction of hexavalent uranium (U),more »i.e., the accumulation of the heavy isotope in the U(IV) phase, is readily distinguishable from that generated by abiotic uranium reduction in laboratory experiments. Thus, isotope signatures preserved in the geologic record through the reductive precipitation of uranium may provide the sought-after tool to probe for biotic processes. Because uranium is a common element in the Earth’s crust and a wide variety of metabolic groups of microorganisms catalyze the biological reduction of U(VI), this tool is applicable to a multiplicity of geological epochs and terrestrial environments. The findings of this study indicate that biological activity contributed to the formation of many authigenic U deposits, including sandstone U deposits of various ages, as well as modern, Cretaceous, and Archean black shales. In addition, engineered bioremediation activities also exhibit a biotic signature, suggesting that, although multiple pathways may be involved in the reduction, direct enzymatic reduction contributes substantially to the immobilization of uranium.« less

  19. Inherently safe in situ uranium recovery.

    SciTech Connect (OSTI)

    Krumhansl, James Lee; Beauheim, Richard Louis; Brady, Patrick Vane; Arnold, Bill Walter; Kanney, Joseph F.; McKenna, Sean Andrew

    2009-05-01

    Expansion of uranium mining in the United States is a concern to some environmental groups and sovereign Native American Nations. An approach which may alleviate some problems is to develop inherently safe in situ uranium recovery ('ISR') technologies. Current ISR technology relies on chemical extraction of trace levels of uranium from aquifers that, once mined, can still contain dissolved uranium and other trace metals that are a health concern. Existing ISR operations are few in number; however, high uranium prices are driving the industry to consider expanding operations nation-wide. Environmental concerns and enforcement of the new 30 ppb uranium drinking water standard may make opening new mining operations more difficult and costly. Here we propose a technological fix: the development of inherently safe in situ recovery (ISISR) methods. The four central features of an ISISR approach are: (1) New 'green' leachants that break down predictably in the subsurface, leaving uranium, and associated trace metals, in an immobile form; (2) Post-leachant uranium/metals-immobilizing washes that provide a backup decontamination process; (3) An optimized well-field design that increases uranium recovery efficiency and minimizes excursions of contaminated water; and (4) A combined hydrologic/geochemical protocol for designing low-cost post-extraction long-term monitoring. ISISR would bring larger amounts of uranium to the surface, leave fewer toxic metals in the aquifer, and cost less to monitor safely - thus providing a 'win-win-win' solution to all stakeholders.

  20. Global terrestrial uranium supply and its policy implications : a probabilistic projection of future uranium costs

    E-Print Network [OSTI]

    Matthews, Isaac A

    2010-01-01

    An accurate outlook on long-term uranium resources is critical in forecasting uranium costresource relationships, and for energy policy planning as regards the development and deployment of nuclear fuel cycle alternatives. ...

  1. Uranium 2009 resources, production and demand

    E-Print Network [OSTI]

    Organisation for Economic Cooperation and Development. Paris

    2010-01-01

    With several countries currently building nuclear power plants and planning the construction of more to meet long-term increases in electricity demand, uranium resources, production and demand remain topics of notable interest. In response to the projected growth in demand for uranium and declining inventories, the uranium industry – the first critical link in the fuel supply chain for nuclear reactors – is boosting production and developing plans for further increases in the near future. Strong market conditions will, however, be necessary to trigger the investments required to meet projected demand. The "Red Book", jointly prepared by the OECD Nuclear Energy Agency and the International Atomic Energy Agency, is a recognised world reference on uranium. It is based on information compiled in 40 countries, including those that are major producers and consumers of uranium. This 23rd edition provides a comprehensive review of world uranium supply and demand as of 1 January 2009, as well as data on global ur...

  2. Uranium Metal Analysis via Selective Dissolution

    SciTech Connect (OSTI)

    Delegard, Calvin H.; Sinkov, Sergey I.; Schmidt, Andrew J.; Chenault, Jeffrey W.

    2008-09-10

    Uranium metal, which is present in sludge held in the Hanford Site K West Basin, can create hazardous hydrogen atmospheres during sludge handling, immobilization, or subsequent transport and storage operations by its oxidation/corrosion in water. A thorough knowledge of the uranium metal concentration in sludge therefore is essential to successful sludge management and waste process design. The goal of this work was to establish a rapid routine analytical method to determine uranium metal concentrations as low as 0.03 wt% in sludge even in the presence of up to 1000-fold higher total uranium concentrations (i.e., up to 30 wt% and more uranium) for samples to be taken during the upcoming sludge characterization campaign and in future analyses for sludge handling and processing. This report describes the experiments and results obtained in developing the selective dissolution technique to determine uranium metal concentration in K Basin sludge.

  3. Depleted uranium disposal options evaluation

    SciTech Connect (OSTI)

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

    1994-05-01

    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.

  4. U.S. And Russia Complete Nuclear Security Upgrades Under Bratislava...

    Office of Environmental Management (EM)

    research reactors internationally fueled with highly enriched uranium (HEU) to low enriched uranium fuel and to return all Russian-origin HEU fresh and spent nuclear fuel stored...

  5. Friday, September 24, 2010 | National Nuclear Security Administration

    National Nuclear Security Administration (NNSA)

    States also disposes of its surplus highly enriched uranium by downblending it to low enriched uranium for peaceful use as commercial nuclear reactor fuel. These programs are a...

  6. IAEA 2010 General Conference Travel Blog | National Nuclear Security...

    National Nuclear Security Administration (NNSA)

    States also disposes of its surplus highly enriched uranium by downblending it to low enriched uranium for peaceful use as commercial nuclear reactor fuel. These programs are a...

  7. DOE F 1325

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

    (NNSA) manages a program for converting surplus highly enriched uranium (HEU) to low enriched uranium (LEU) suitable for use in commercial nuclear reactors. Under this program,...

  8. heu

    National Nuclear Security Administration (NNSA)

    plans to reduce the proliferation threat from stockpiles of surplus highly enriched uranium (HEU) by down-blending, or converting, it to low enriched uranium (LEU). In this...

  9. 2014 Uranium Marketing Annual Report

    U.S. Energy Information Administration (EIA) 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| Open Energy Informationmonthly gasoline price to fall toUranium Marketing Annual Report 2014

  10. Decay Heat Calculations for PWR and BWR Assemblies Fueled with Uranium and Plutonium Mixed Oxide Fuel using SCALE

    SciTech Connect (OSTI)

    Ade, Brian J; Gauld, Ian C

    2011-10-01

    In currently operating commercial nuclear power plants (NPP), there are two main types of nuclear fuel, low enriched uranium (LEU) fuel, and mixed-oxide uranium-plutonium (MOX) fuel. The LEU fuel is made of pure uranium dioxide (UO{sub 2} or UOX) and has been the fuel of choice in commercial light water reactors (LWRs) for a number of years. Naturally occurring uranium contains a mixture of different uranium isotopes, primarily, {sup 235}U and {sup 238}U. {sup 235}U is a fissile isotope, and will readily undergo a fission reaction upon interaction with a thermal neutron. {sup 235}U has an isotopic concentration of 0.71% in naturally occurring uranium. For most reactors to maintain a fission chain reaction, the natural isotopic concentration of {sup 235}U must be increased (enriched) to a level greater than 0.71%. Modern nuclear reactor fuel assemblies contain a number of fuel pins potentially having different {sup 235}U enrichments varying from {approx}2.0% to {approx}5% enriched in {sup 235}U. Currently in the United States (US), all commercial nuclear power plants use UO{sub 2} fuel. In the rest of the world, UO{sub 2} fuel is still commonly used, but MOX fuel is also used in a number of reactors. MOX fuel contains a mixture of both UO{sub 2} and PuO{sub 2}. Because the plutonium provides the fissile content of the fuel, the uranium used in MOX is either natural or depleted uranium. PuO{sub 2} is added to effectively replace the fissile content of {sup 235}U so that the level of fissile content is sufficiently high to maintain the chain reaction in an LWR. Both reactor-grade and weapons-grade plutonium contains a number of fissile and non-fissile plutonium isotopes, with the fraction of fissile and non-fissile plutonium isotopes being dependent on the source of the plutonium. While only RG plutonium is currently used in MOX, there is the possibility that WG plutonium from dismantled weapons will be used to make MOX for use in US reactors. Reactor-grade plutonium in MOX fuel is generally obtained from reprocessed irradiated nuclear fuel, whereas weapons-grade plutonium is obtained from decommissioned nuclear weapons material and thus has a different plutonium (and other actinides) concentration. Using MOX fuel instead of UOX fuel has potential impacts on the neutronic performance of the nuclear fuel and the design of the nuclear fuel must take these differences into account. Each of the plutonium sources (RG and WG) has different implications on the neutronic behavior of the fuel because each contains a different blend of plutonium nuclides. The amount of heat and the number of neutrons produced from fission of plutonium nuclides is different from fission of {sup 235}U. These differences in UOX and MOX do not end at discharge of the fuel from the reactor core - the short- and long-term storage of MOX fuel may have different requirements than UOX fuel because of the different discharged fuel decay heat characteristics. The research documented in this report compares MOX and UOX fuel during storage and disposal of the fuel by comparing decay heat rates for typical pressurized water reactor (PWR) and boiling water reactor (BWR) fuel assemblies with and without weapons-grade (WG) and reactor-grade (RG) MOX fuel.

  11. Dry process fluorination of uranium dioxide using ammonium bifluoride

    E-Print Network [OSTI]

    Yeamans, Charles Burnett, 1978-

    2003-01-01

    An experimental study was conducted to determine the practicality of various unit operations for fluorination of uranium dioxide. The objective was to prepare ammonium uranium fluoride double salts from uranium dioxide and ...

  12. THE THEORY OF URANIUM ENRICHMENT BY THE GAS CENTRIFUGE

    E-Print Network [OSTI]

    Olander, Donald R.

    2013-01-01

    E. (1973) "Uranium Enrichment by Gas Centrifuge" Mills andTHEORY OF URANIUM ENRICHMENT BY THE GAS CENTRIFUGE Donald R.THEORY OF URANIUM ENRICHMENT BY THE GAS CENTRIFUGE by Donald

  13. Colorimetric detection of uranium in water

    DOE Patents [OSTI]

    DeVol, Timothy A. (Clemson, SC); Hixon, Amy E. (Piedmont, SC); DiPrete, David P. (Evans, GA)

    2012-03-13

    Disclosed are methods, materials and systems that can be used to determine qualitatively or quantitatively the level of uranium contamination in water samples. Beneficially, disclosed systems are relatively simple and cost-effective. For example, disclosed systems can be utilized by consumers having little or no training in chemical analysis techniques. Methods generally include a concentration step and a complexation step. Uranium concentration can be carried out according to an extraction chromatographic process and complexation can chemically bind uranium with a detectable substance such that the formed substance is visually detectable. Methods can detect uranium contamination down to levels even below the MCL as established by the EPA.

  14. Final Uranium Leasing Program Programmatic Environmental Impact...

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

    Tribe 11 12 Title: Final Uranium Leasing Program Programmatic Environmental Impact Statement 13 (DOEEIS-0472) 14 15 For additional information on this Programmatic...

  15. High strength and density tungsten-uranium alloys

    DOE Patents [OSTI]

    Sheinberg, Haskell (Los Alamos, NM)

    1993-01-01

    Alloys of tungsten and uranium and a method for making the alloys. The amount of tungsten present in the alloys is from about 55 vol % to about 85 vol %. A porous preform is made by sintering consolidated tungsten powder. The preform is impregnated with molten uranium such that (1) uranium fills the pores of the preform to form uranium in a tungsten matrix or (2) uranium dissolves portions of the preform to form a continuous uranium phase containing tungsten particles.

  16. Sequestering Uranium from Seawater: Binding Strength and Modes...

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

    Sequestering Uranium from Seawater: Binding Strength and Modes of Uranyl Complexes with Glutarimidedioxime Sequestering Uranium from Seawater: Binding Strength and Modes of Uranyl...

  17. 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...

  18. Department of Energy to Continue Managing Uranium Leasing Program...

    Energy Savers [EERE]

    Department of Energy to Continue Managing Uranium Leasing Program in Western Colorado Department of Energy to Continue Managing Uranium Leasing Program in Western Colorado May 12,...

  19. DOE Extends Public Comment Period for the Draft Uranium Leasing...

    Energy Savers [EERE]

    Extends Public Comment Period for the Draft Uranium Leasing Program Programmatic Environmental Impact Statement DOE Extends Public Comment Period for the Draft Uranium Leasing...

  20. Decommissioning of U.S. Uranium Production Facilities

    Reports and Publications (EIA)

    1995-01-01

    This report analyzes the uranium production facility decommissioning process and its potential impact on uranium supply and prices. 1995 represents the most recent publication year.

  1. Secretarial Determination of No Adverse Material Impact for Uranium...

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

    Secretarial Determination of No Adverse Material Impact for Uranium Transfers Secretarial Determination of No Adverse Material Impact for Uranium Transfers The determination covers...

  2. 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...

  3. DOE Extends Public Comment Period for Uranium Program Environmental...

    Office of Environmental Management (EM)

    Uranium Program Environmental Impact Statement DOE Extends Public Comment Period for Uranium Program Environmental Impact Statement April 18, 2013 - 1:08pm Addthis Contractor, Bob...

  4. DOE Seeks Contractor for Depleted Uranium Hexafluoride (DUF6...

    Energy Savers [EERE]

    DOE Seeks Contractor for Depleted Uranium Hexafluoride (DUF6) Operations at Ohio and Kentucky Facilities DOE Seeks Contractor for Depleted Uranium Hexafluoride (DUF6) Operations at...

  5. Record of Decision for the Uranium Leasing Program Programmatic...

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

    Record of Decision for the Uranium Leasing Program Programmatic Environmental Impact Statement Record of Decision for the Uranium Leasing Program Programmatic Environmental Impact...

  6. Uranium Speciation As a Function of Depth in Contaminated Hanford...

    Office of Scientific and Technical Information (OSTI)

    PLUMES; PONDS; SEDIMENTS; SILICATE MINERALS; SODIUM; SPECTRA; SPECTROSCOPY; SURFACE COATING; URANIUM; URANIUM MINERALS; WASTES; WATER TABLES Word Cloud More Like This Full Text...

  7. Control of structure and reactivity by ligand design : applications to small molecule activation by low-valent uranium complexes

    E-Print Network [OSTI]

    Lam, Oanh Phi

    2010-01-01

    Coordination Chemistry of Uranium………………………………….11 1.4researchers from uranium chemistry. Fortunately, despiteclassical coordination chemistry of uranium has flourished

  8. Uranium Management - Preservation of a National Asset

    SciTech Connect (OSTI)

    Jackson, J. D.; Stroud, J. C.

    2002-02-27

    The Uranium Management Group (UMG) was established at the Department of Energy's (DOE's) Oak Ridge Operations in 1999 as a mechanism to expedite the de-inventory of surplus uranium from the Fernald Environmental Management Project site. This successful initial venture has broadened into providing uranium material de-inventory and consolidation support to the Hanford site as well as retrieving uranium materials that the Department had previously provided to universities under the loan/lease program. As of December 31, 2001, {approx} 4,300 metric tons of uranium (MTU) have been consolidated into a more cost effective interim storage location at the Portsmouth site near Piketon, OH. The UMG continues to uphold its corporate support mission by promoting the Nuclear Materials Stewardship Initiative (NMSI) and the twenty-five (25) action items of the Integrated Nuclear Materials Management Plan (1). Before additional consolidation efforts may commence to remove excess inventory from Environmental Management closure sites and universities, a Programmatic Environmental Assessment (PEA) must be completed. Two (2) noteworthy efforts currently being pursued involve the investigation of re-use opportunities for surplus uranium materials and the recovery of usable uranium from the shutdown Portsmouth cascade. In summary, the UMG is available as a DOE complex-wide technical resource to promote the responsible management of surplus uranium.

  9. Clean Air Act Requirements: Uranium Mill Tailings

    E-Print Network [OSTI]

    EPA'S Clean Air Act Requirements: Uranium Mill Tailings Radon Emissions Rulemaking Reid J. Rosnick Requirements for Uranium Operations (Clean Air Act) Subpart W Requirements (continued) · Radon emission standard of 20 pCi/m2/sec -- annual reporting requirements, notification in advance of testing · The radon

  10. Molten-Salt Depleted-Uranium Reactor

    E-Print Network [OSTI]

    Dong, Bao-Guo; Gu, Ji-Yuan

    2015-01-01

    The supercritical, reactor core melting and nuclear fuel leaking accidents have troubled fission reactors for decades, and greatly limit their extensive applications. Now these troubles are still open. Here we first show a possible perfect reactor, Molten-Salt Depleted-Uranium Reactor which is no above accident trouble. We found this reactor could be realized in practical applications in terms of all of the scientific principle, principle of operation, technology, and engineering. Our results demonstrate how these reactors can possess and realize extraordinary excellent characteristics, no prompt critical, long-term safe and stable operation with negative feedback, closed uranium-plutonium cycle chain within the vessel, normal operation only with depleted-uranium, and depleted-uranium high burnup in reality, to realize with fission nuclear energy sufficiently satisfying humanity long-term energy resource needs, as well as thoroughly solve the challenges of nuclear criticality safety, uranium resource insuffic...

  11. Method for fabricating laminated uranium composites

    DOE Patents [OSTI]

    Chapman, L.R.

    1983-08-03

    The present invention is directed to a process for fabricating laminated composites of uranium or uranium alloys and at least one other metal or alloy. The laminated composites are fabricated by forming a casting of the molten uranium with the other metal or alloy which is selectively positioned in the casting and then hot-rolling the casting into a laminated plate in or around which the casting components are metallurgically bonded to one another to form the composite. The process of the present invention provides strong metallurgical bonds between the laminate components primarily since the bond disrupting surface oxides on the uranium or uranium alloy float to the surface of the casting to effectively remove the oxides from the bonding surfaces of the components.

  12. Scrap uranium recycling via electron beam melting

    SciTech Connect (OSTI)

    McKoon, R.

    1993-11-01

    A program is underway at the Lawrence Livermore National Laboratory (LLNL) to recycle scrap uranium metal. Currently, much of the material from forging and machining processes is considered radioactive waste and is disposed of by oxidation and encapsulation at significant cost. In the recycling process, uranium and uranium alloys in various forms will be processed by electron beam melting and continuously cast into ingots meeting applicable specifications for virgin material. Existing vacuum processing facilities at LLNL are in compliance with all current federal and state environmental, safety and health regulations for the electron beam melting and vaporization of uranium metal. One of these facilities has been retrofitted with an auxiliary electron beam gun system, water-cooled hearth, crucible and ingot puller to create an electron beam melt furnace. In this furnace, basic process R&D on uranium recycling will be performed with the goal of eventual transfer of this technology to a production facility.

  13. Thermodynamic data for uranium fluorides

    SciTech Connect (OSTI)

    Leitnaker, J.M.

    1983-03-01

    Self-consistent thermodynamic data have been tabulated for uranium fluorides between UF/sub 4/ and UF/sub 6/, including UF/sub 4/ (solid and gas), U/sub 4/F/sub 17/ (solid), U/sub 2/F/sub 9/ (solid), UF/sub 5/ (solid and gas), U/sub 2/F/sub 10/ (gas), and UF/sub 6/ (solid, liquid, and gas). Included are thermal function - the heat capacity, enthalpy, and free energy function, heats of formation, and vaporization behavior.

  14. 2014 Domestic Uranium Production Report

    U.S. Energy Information Administration (EIA) 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: AlternativeMonthly","10/2015"Monthly","10/2015" ,"Release7 Relative Standard Errors for Relative StandardCensusp2. U.S. uranium

  15. Uranium Cluster Chemistry DOI: 10.1002/anie.200906605

    E-Print Network [OSTI]

    Uranium Cluster Chemistry DOI: 10.1002/anie.200906605 Tetranuclear Uranium Clusters by Reductive in the coordination chemistry and small-molecule reactivity of uranium. Among the intriguing reactivity patterns of tetravalent uranium with 3,5-dimethylpyrazolate (Me2PzÀ ) led to forma- tion of an unprecedented homoleptic

  16. The Homopolar Pulse Billet Heating Process 

    E-Print Network [OSTI]

    Keith, R. E.; Weldon, W. F.

    1982-01-01

    ., Rylander, H. G., and Woodson, H. H., "Feasibility Study of Pipe Welding ~'- "Inertial Energy Storage Research at Using a Homopolar Generator", Electric The University of Texas at Austin", Power Research Institute Rept. No. IEEE Int'l. Pulsed Power Conf... and Design, Fabrication, and Testing of a Topological Considerations for Fast Five Megajoule Homopolar Discharge Homopolar Machines", IEEE Motor-Generator", Int'l. Conf. on Int'l. Conf. on Plasma Science, Ann Energy Storage, Comp~ession, and Arbor, MI...

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

    SciTech Connect (OSTI)

    N /A

    2003-11-28

    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.

  18. Technical Basis for Assessing Uranium Bioremediation Performance

    SciTech Connect (OSTI)

    PE Long; SB Yabusaki; PD Meyer; CJ Murray; AL N’Guessan

    2008-04-01

    In situ bioremediation of uranium holds significant promise for effective stabilization of U(VI) from groundwater at reduced cost compared to conventional pump and treat. This promise is unlikely to be realized unless researchers and practitioners successfully predict and demonstrate the long-term effectiveness of uranium bioremediation protocols. Field research to date has focused on both proof of principle and a mechanistic level of understanding. Current practice typically involves an engineering approach using proprietary amendments that focuses mainly on monitoring U(VI) concentration for a limited time period. Given the complexity of uranium biogeochemistry and uranium secondary minerals, and the lack of documented case studies, a systematic monitoring approach using multiple performance indicators is needed. This document provides an overview of uranium bioremediation, summarizes design considerations, and identifies and prioritizes field performance indicators for the application of uranium bioremediation. The performance indicators provided as part of this document are based on current biogeochemical understanding of uranium and will enable practitioners to monitor the performance of their system and make a strong case to clients, regulators, and the public that the future performance of the system can be assured and changes in performance addressed as needed. The performance indicators established by this document and the information gained by using these indicators do add to the cost of uranium bioremediation. However, they are vital to the long-term success of the application of uranium bioremediation and provide a significant assurance that regulatory goals will be met. The document also emphasizes the need for systematic development of key information from bench scale tests and pilot scales tests prior to full-scale implementation.

  19. Stratigraphy of the PB-1 well, Nopal I uranium deposit, Sierra Pena Blanca, Chihuahua, Mexico

    E-Print Network [OSTI]

    Dobson, P.

    2009-01-01

    of the Nopal I uranium deposit, Mexico: Proceedings, 2006of the Nopal I uranium deposit (Sierra Peña Blanca, Mexico),Chihuahua, Mexico, in Uranium Deposits in Volcanic Rocks,

  20. Electrochemistry, Spectroscopy, and Reactivity of Uranium Complexes Supported by Ferrocene Diamide Ligands

    E-Print Network [OSTI]

    Duhovic, Selma

    2012-01-01

    J. L. , Pentavalent Uranium Chemistry-Synthetic Pursuit of aand High-Valent Uranium Chemistry. Organometallics 2011,for Trivalent Uranium Chemistry. Inorg. Chem. 1989, 28, (

  1. Behavior of Uranium(VI) during HEDPA Leaching for Aluminum Dissolution in Tank Waste Sludges

    E-Print Network [OSTI]

    Powell, Brian A.; Rao, Linfeng; Nash, Kenneth L.; Martin, Leigh

    2006-01-01

    Behavior of Uranium(VI) during HEDPA Leaching for Aluminuman increase in the aqueous phase uranium concentration.The concentration of uranium continually increased over 59

  2. In-well sediment incubators to evaluate microbial community stability and dynamics following bioimmobilization of uranium

    E-Print Network [OSTI]

    Baldwin, B.R.

    2010-01-01

    D. R. (1992). Enzymatic uranium precipitation. Environmentalof technetium and uranium in a nitrate-contaminated aquifer.in situ bioremediation of uranium-contaminated groundwater.

  3. Sequestering Uranium from Seawater: Binding Strength and Modes of Uranyl Complexes with Glutarimidedioxime

    E-Print Network [OSTI]

    Tian, Guoxin

    2013-01-01

    data_request/cif. OECD, Uranium 2009: Resources, Productionthermodynamics of uranium”, (H. Wanner and I. Forest,of California. Sequestering uranium from seawater: binding

  4. Sulfur isotopes as indicators of amended bacterial sulfate reduction processes influencing field scale uranium bioremediation

    E-Print Network [OSTI]

    Druhan, J.L.

    2009-01-01

    in situ bioremediation of uranium in a highly contaminatedwith bioremediation of uranium to submicromolar levels.Reoxidation of bioreduced uranium under reducing conditions.

  5. Stability of uranium incorporated into Fe(hydr)oxides under fluctuating redox conditions

    E-Print Network [OSTI]

    Stewart, B.D.

    2009-01-01

    for Bioremediation of uranium-contaminated aquifers withReoxidation of bioreduced uranium under reducing conditions.Komlos, J. ; Jaffe, P. R. Uranium reoxidation in previously

  6. Decolonizing cartographies : sovereignty, territoriality, and maps of meaning in the uranium landscape

    E-Print Network [OSTI]

    Voyles, Traci Brynne

    2010-01-01

    Figure 8 Colorado Plateau uranium district, Life magazine in146! Figure 12 Navajo Nation and uranium industry162! Figure 14 An undated poster protesting uranium

  7. Inherently safe in situ uranium recovery (Patent) | SciTech Connect

    Office of Scientific and Technical Information (OSTI)

    Inherently safe in situ uranium recovery Citation Details In-Document Search Title: Inherently safe in situ uranium recovery An in situ recovery of uranium operation involves...

  8. Incorporation of oxidized uranium into Fe (hydr)oxides during Fe(II) catalyzed remineralization

    E-Print Network [OSTI]

    Nico, Peter S.

    2010-01-01

    B. M. ; Geesey, G. G. Uranium complexes formed at hematiteheterogeneity in an in situ uranium bioremediation fieldL. R. In-situ evidence for uranium immobilization and

  9. Novel Transformations using Uranium and Group 5 Metal Complexes Supported by 1,1'-diamidoferrocene Ligands

    E-Print Network [OSTI]

    Lopez, Michael Joseph

    2013-01-01

    in the past decade. 1 Uranium is the most studiedactinide, due the stability of uranium-238and uranium involvement in nuclear power. Despite interest

  10. Uranium-series comminution ages of continental sediments: Case study of a Pleistocene alluvial fan

    E-Print Network [OSTI]

    Lee, Victoria E.

    2010-01-01

    and river transport. Uranium-Series Geochemistry 52, 533-using high- precision uranium isotopic measurements.B. , Turner, S.P. , 2008. Uranium-series isotopes in river

  11. Magnetic Exchange Coupling and Single-Molecule Magnetism in Uranium Complexes

    E-Print Network [OSTI]

    Rinehart, Jeffrey Dennis

    2010-01-01

    method for interpreting uranium magnetism and will becontaining lower-valent uranium centers can be seen to1995. Chapter 4: Tetranuclear Uranium Clusters via Reductive

  12. Decolonizing cartographies : sovereignty, territoriality, and maps of meaning in the uranium landscape

    E-Print Network [OSTI]

    Voyles, Traci Brynne

    2010-01-01

    uranium mining .. 176!Doug, “The History of Uranium Mining and the Navajo People,”The Navajo People and Uranium Mining, University of New

  13. Electrolytic process for preparing uranium metal

    DOE Patents [OSTI]

    Haas, Paul A. (Knoxville, TN)

    1990-01-01

    An electrolytic process for making uranium from uranium oxide using Cl.sub.2 anode product from an electrolytic cell to react with UO.sub.2 to form uranium chlorides. The chlorides are used in low concentrations in a melt comprising fluorides and chlorides of potassium, sodium and barium in the electrolytic cell. The electrolysis produces Cl.sub.2 at the anode that reacts with UO.sub.2 in the feed reactor to form soluble UCl.sub.4, available for a continuous process in the electrolytic cell, rather than having insoluble UO.sub.2 fouling the cell.

  14. 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefield Municipal GasAdministration Medal01 Sandia4)9 FederalRivers andMEDA Station3/%2A ¡BLM Public

  15. Uranium isotopic composition and uranium concentration in special reference material SRM A (uranium in KCl/LiCl salt matrix)

    SciTech Connect (OSTI)

    Graczyk, D.G.; Essling, A.M.; Sabau, C.S.; Smith, F.P.; Bowers, D.L.; Ackerman, J.P.

    1997-07-01

    To help assure that analysis data of known quality will be produced in support of demonstration programs at the Fuel Conditioning Facility at Argonne National Laboratory-West (Idaho Falls, ID), a special reference material has been prepared and characterized. Designated SRM A, the material consists of individual units of LiCl/KCl eutectic salt containing a nominal concentration of 2.5 wt. % enriched uranium. Analyses were performed at Argonne National Laboratory-East (Argonne, IL) to determine the uniformity of the material and to establish reference values for the uranium concentration and uranium isotopic composition. Ten units from a batch of approximately 190 units were analyzed by the mass spectrometric isotope dilution technique to determine their uranium concentration. These measurements provided a mean value of 2.5058 {+-} 0.0052 wt. % U, where the uncertainty includes estimated limits to both random and systematic errors that might have affected the measurements. Evidence was found of a small, apparently random, non-uniformity in uranium content of the individual SRM A units, which exhibits a standard deviation of 0.078% of the mean uranium concentration. Isotopic analysis of the uranium from three units, by means of thermal ionization mass spectrometry with a special, internal-standard procedure, indicated that the uranium isotopy is uniform among the pellets with a composition corresponding to 0.1115 {+-} 0.0006 wt. % {sup 234}U, 19.8336 {+-} 0.0059 wt. % {sup 235}U, 0.1337 {+-} 0.0006 wt. % {sup 236}U, and 79.9171 {+-} 0.0057 wt. % {sup 238}U.

  16. Thermodynamic properties of uranium dioxide

    SciTech Connect (OSTI)

    Fink, J.K.; Chasanov, M.G.; Leibowitz, L.

    1981-04-01

    In order to provide reliable and consistent data on the thermophysical properties of reactor materials for reactor safety studies, this revision is prepared for the thermodynamic properties of the uranium dioxide portion of the fuel property section of the report Properties for LMFBR Safety Analysis. Since the original report was issued in 1976, there has been international agreement on a vapor pressure equation for the total pressure over UO/sub 2/, new methods have been suggested for the calculation of enthalpy and heat capacity, and a phase change at 2670 K has been proposed. In this report, an electronic term is used in place of the Frenkel defect term in the enthalpy and heat capacity equation and the phase transition is accepted.

  17. Highly Enriched Uranium Disposition | National Nuclear Security...

    National Nuclear Security Administration (NNSA)

    NNSA seeks to recover the economic value of the material by using the resulting LEU as nuclear reactor fuel. U.S.-Russian Highly Enriched Uranium Purchase Agreement NNSA's HEU...

  18. Process for reducing beta activity in uranium

    DOE Patents [OSTI]

    Briggs, G.G.; Kato, T.R.; Schonegg, E.

    1985-04-11

    This invention is a method for lowering the beta radiation hazards associated with the casting of uranium. The method reduces the beta radiation emitted from the as-cast surfaces of uranium ingots. The method also reduces the amount of beta radiation emitters retained on the interiors of the crucibles that have been used to melt the uranium charges and which undergone cleaning in a remote handling facility. The lowering of the radioactivity is done by scavenging the beta emitters from the molten uranium with a molten mixture containing the fluorides of magnesium and calcium. The method provides a means of collection and disposal of the beta emitters in a manner that reduces radiation exposure to operating personnel in the work area where the ingots are cast and processed. 5 tabs.

  19. U.S. Uranium Reserves Estimates

    Gasoline and Diesel Fuel Update (EIA)

    1. U.S. Forward-Cost Uranium Reserves by State, Year-End 2008 State 50lb 100lb Ore (million tons) Gradea (%) U3O8 (million lbs) Ore (million tons) Gradea (%) U3O8 (million lbs)...

  20. Process for reducing beta activity in uranium

    DOE Patents [OSTI]

    Briggs, Gifford G. (Cincinnatti, OH); Kato, Takeo R. (Cincinnatti, OH); Schonegg, Edward (Cleves, OH)

    1986-01-01

    This invention is a method for lowering the beta radiation hazards associated with the casting of uranium. The method reduces the beta radiation emitted from the as-cast surfaces of uranium ingots. The method also reduces the amount of beta radiation emitters retained on the interiors of the crucibles that have been used to melt the uranium charges and which have undergone cleaning in a remote handling facility. The lowering of the radioactivity is done by scavenging the beta emitters from the molten uranium with a molten mixture containing the fluorides of magnesium and calcium. The method provides a means of collection and disposal of the beta emitters in a manner that reduces radiation exposure to operating personnel in the work area where the ingots are cast and processed.

  1. U.S. Uranium Reserves Estimates

    Gasoline and Diesel Fuel Update (EIA)

    Methodology The U.S. uranium ore reserves reported by EIA for specific MFC categories represent the sums of quantities estimated to occur in known deposits on properties where data...

  2. U.S. Uranium Reserves Estimates

    Gasoline and Diesel Fuel Update (EIA)

    2. U.S. Forward-Cost Uranium Reserves by Mining Method, Year-End 2008 Mining Method 50 per pound 100 per pound Ore (million tons) Gradea (percent U3O8) U3O8 (million pounds) Ore...

  3. Innovative design of uranium startup fast reactors

    E-Print Network [OSTI]

    Fei, Tingzhou

    2012-01-01

    Sodium Fast Reactors are one of the three candidates of GEN-IV fast reactors. Fast reactors play an important role in saving uranium resources and reducing nuclear wastes. Conventional fast reactors rely on transuranic ...

  4. Decommissioning of uranium mines in Canada

    SciTech Connect (OSTI)

    Zgola, M.B. [Atomic Energy Control Board, Ottawa, Ontario (Canada)

    1996-12-31

    The Atomic Energy Control Board (AECB) regulates the nuclear fuel cycle in Canada. This paper overviews the nature and function of the AECB; discusses its {open_quotes}site-specific{close_quotes} approach to regulating the decommissioning of uranium mining facilities; catalogues the location and status of inactive uranium tailings impoundments in Canada; and, summarizes the decommissioning work at the licensed Elliot Lake tailings impoundments.

  5. The ultimate disposition of depleted uranium

    SciTech Connect (OSTI)

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

    1991-12-31

    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.

  6. Depleted uranium: A DOE management guide

    SciTech Connect (OSTI)

    1995-10-01

    The U.S. Department of Energy (DOE) has a management challenge and financial liability in the form of 50,000 cylinders containing 555,000 metric tons of depleted uranium hexafluoride (UF{sub 6}) that are stored at the gaseous diffusion plants. The annual storage and maintenance cost is approximately $10 million. This report summarizes several studies undertaken by the DOE Office of Technology Development (OTD) to evaluate options for long-term depleted uranium management. Based on studies conducted to date, the most likely use of the depleted uranium is for shielding of spent nuclear fuel (SNF) or vitrified high-level waste (HLW) containers. The alternative to finding a use for the depleted uranium is disposal as a radioactive waste. Estimated disposal costs, utilizing existing technologies, range between $3.8 and $11.3 billion, depending on factors such as applicability of the Resource Conservation and Recovery Act (RCRA) and the location of the disposal site. The cost of recycling the depleted uranium in a concrete based shielding in SNF/HLW containers, although substantial, is comparable to or less than the cost of disposal. Consequently, the case can be made that if DOE invests in developing depleted uranium shielded containers instead of disposal, a long-term solution to the UF{sub 6} problem is attained at comparable or lower cost than disposal as a waste. Two concepts for depleted uranium storage casks were considered in these studies. The first is based on standard fabrication concepts previously developed for depleted uranium metal. The second converts the UF{sub 6} to an oxide aggregate that is used in concrete to make dry storage casks.

  7. Electrochemical method of producing eutectic uranium alloy and apparatus

    DOE Patents [OSTI]

    Horton, James A. (Livermore, CA); Hayden, H. Wayne (Oakridge, TN)

    1995-01-01

    An apparatus and method for continuous production of liquid uranium alloys through the electrolytic reduction of uranium chlorides. The apparatus includes an electrochemical cell formed from an anode shaped to form an electrolyte reservoir, a cathode comprising a metal, such as iron, capable of forming a eutectic uranium alloy having a melting point less than the melting point of pure uranium, and molten electrolyte in the reservoir comprising a chlorine or fluorine containing salt and uranium chloride. The method of the invention produces an eutectic uranium alloy by creating an electrolyte reservoir defined by a container comprising an anode, placing an electrolyte in the reservoir, the electrolyte comprising a chlorine or fluorine containing salt and uranium chloride in molten form, positioning a cathode in the reservoir where the cathode comprises a metal capable of forming an uranium alloy having a melting point less than the melting point of pure uranium, and applying a current between the cathode and the anode.

  8. Stability of uranium incorporated into Fe(hydr)oxides under fluctuating redox conditions

    E-Print Network [OSTI]

    Stewart, B.D.

    2009-01-01

    at the Koongarra uranium deposit, Northern Australia -Uranium isotopic evidence for the origin of the Bahariya iron deposits,

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

    SciTech Connect (OSTI)

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

    2009-07-04

    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.

  10. Spain`s uranium industry

    SciTech Connect (OSTI)

    Ferguson, M.P.

    1992-05-01

    Spain currently operates nine nuclear reactors totalling over 7,100 MWe of capacity, contributing about one-third of all electricity generated in Spain. Four reactors at advanced stages of construction remain mothballed as the result of a government-imposed moratorium, and a fire at Vandellos 1 in 1989 led to its premature closure and to a revival of anti-nuclear sentiment in the country. In the new national energy plan, which was sent to the Spanish Parliament on July 25, 1991, Spain opted to continue the nuclear moratorium that began in 1984 and rely upon conservation measures, additional natural gas imports, and electricity imports to meet expected demand. Under the new plan, nuclear power`s share of Spain`s total installed electrical generating capacity will fall from about 17 percent in 1990, to approximately 14 percent by the end of the century, as only the current nuclear facilities will continue to operate and no new nuclear plants will be built. Spain`s integration into the European Community also is affecting the country`s energy plans, prompting consolidation within the Spanish electricity sector in order to be more competitive in Europe. To supply the existing reactors, the government is supporting a major expansion of the country`s domestic uranium industry.

  11. Uranium mill ore dust characterization

    SciTech Connect (OSTI)

    Knuth, R.H.; George, A.C.

    1980-11-01

    Cascade impactor and general air ore dust measurements were taken in a uranium processing mill in order to characterize the airborne activity, the degree of equilibrium, the particle size distribution and the respirable fraction for the /sup 238/U chain nuclides. The sampling locations were selected to limit the possibility of cross contamination by airborne dusts originating in different process areas of the mill. The reliability of the modified impactor and measurement techniques was ascertained by duplicate sampling. The results reveal no significant deviation from secular equilibrium in both airborne and bulk ore samples for the /sup 234/U and /sup 230/Th nuclides. In total airborne dust measurements, the /sup 226/Ra and /sup 210/Pb nuclides were found to be depleted by 20 and 25%, respectively. Bulk ore samples showed depletions of 10% for the /sup 226/Ra and /sup 210/Pb nuclides. Impactor samples show disequilibrium of /sup 226/Ra as high as +-50% for different size fractions. In these samples the /sup 226/Ra ratio was generally found to increase as particle size decreased. Activity median aerodynamic diameters of the airborne dusts ranged from 5 to 30 ..mu..m with a median diameter of 11 ..mu..m. The maximum respirable fraction for the ore dusts, based on the proposed International Commission on Radiological Protection's (ICRP) definition of pulmonary deposition, was < 15% of the total airborne concentration. Ore dust parameters calculated for impactor duplicate samples were found to be in excellent agreement.

  12. RESOLUTION OF URANIUM ISOTOPES WITH KINETIC PHOSPHORESCENCE ANALYSIS

    SciTech Connect (OSTI)

    Miley, Sarah M.; Hylden, Anne T.; Friese, Judah I.

    2013-04-01

    This study was conducted to test the ability of the Chemchek™ Kinetic Phosphorescence Analyzer Model KPA-11 with an auto-sampler to resolve the difference in phosphorescent decay rates of several different uranium isotopes, and therefore identify the uranium isotope ratios present in a sample. Kinetic phosphorescence analysis (KPA) is a technique that provides rapid, accurate, and precise determination of uranium concentration in aqueous solutions. Utilizing a pulsed-laser source to excite an aqueous solution of uranium, this technique measures the phosphorescent emission intensity over time to determine the phosphorescence decay profile. The phosphorescence intensity at the onset of decay is proportional to the uranium concentration in the sample. Calibration with uranium standards results in the accurate determination of actual concentration of the sample. Different isotopes of uranium, however, have unique properties which should result in different phosphorescence decay rates seen via KPA. Results show that a KPA is capable of resolving uranium isotopes.

  13. Depleted Uranium Hexafluoride (DUF6) Fully Operational at the...

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

    Jack Zimmerman, DUF6 at the PortsmouthPaducah Project Office. DUF6 is depleted uranium hexafluoride, a byproduct of uranium enrichment that has taken place at U.S. gaseous...

  14. EA-1290: Disposition of Russian Federation Titled Natural Uranium

    Broader source: Energy.gov [DOE]

    This EA evaluates the potential environmental impacts of a proposal to transport up to an average of 9,000 metric tons per year of natural uranium as uranium hexafluoride (UF6) from the United...

  15. ORNL/TM-2009/110 Profile of World Uranium

    E-Print Network [OSTI]

    Pennycook, Steve

    ORNL/TM-2009/110 Profile of World Uranium Enrichment Programs--2009 April 2009 Prepared by M. D PROFILE OF WORLD URANIUM ENRICHMENT PROGRAMS--2009 M. D. Laughter Date Published: April 2009 This work

  16. Prospects for the recovery of uranium from seawater

    E-Print Network [OSTI]

    Best, F. R.

    1980-01-01

    A computer program entitled URPE (Uranium Recovery Performance and Economics) has been developed to simulate the engineering performance and provide an economic analysis O of a plant recovering uranium from seawater. The ...

  17. Assessments of long-term uranium supply availability

    E-Print Network [OSTI]

    Zaterman, Daniel R

    2009-01-01

    The future viability of nuclear power will depend on the long-term availability of uranium. A two-form uranium supply model was used to estimate the date at which peak production will occur. The model assumes a constant ...

  18. Electron Microbeam Investigation of Uranium-Contaminated Soils from

    E-Print Network [OSTI]

    Zhu, Chen

    . Uranium(VI), which typically occurs in the uranyl (UO2 2+) ion or in uranyl complexes, dominates under

  19. Monitoring Uranium Transformations Determined by the Evolution of Biogeochemical Processes

    SciTech Connect (OSTI)

    Marsh, Terence L.

    2013-07-30

    Our contribution to the larger project (ANL) was the phylogenetic analysis of evolved communities capable of reducing metals including uranium.

  20. The Uranium Processing Facility (UPF) Finite Element Meshing Discussion

    Broader source: Energy.gov [DOE]

    The Uranium Processing Facility (UPF) Finite Element Meshing Discussion Loring Wyllie Arne Halterman Degenkolb Engineers, San Francisco

  1. Modeling Uranium-Proton Ion Exchange in Biosorption

    E-Print Network [OSTI]

    Volesky, Bohumil

    Modeling Uranium-Proton Ion Exchange in Biosorption J I N B A I Y A N G A N D B O H U M I L V O L E, Quebec, Canada H3A 2B2 Biosorption of uranium metal ions by a nonliving protonated Sargassum fluitans seaweed biomass was used to remove the heavy metal uranium from the aqueous solution. Uranium biosorption

  2. Retrieval of buried depleted uranium from the T-1 trench

    SciTech Connect (OSTI)

    Burmeister, M.; Castaneda, N.; Greengard, T. |; Hull, C.; Barbour, D.; Quapp, W.J.

    1998-07-01

    The Trench 1 remediation project will be conducted this year to retrieve depleted uranium and other associated materials from a trench at Rocky Flats Environmental Technology Site. The excavated materials will be segregated and stabilized for shipment. The depleted uranium will be treated at an offsite facility which utilizes a novel approach for waste minimization and disposal through utilization of a combination of uranium recycling and volume efficient uranium stabilization.

  3. The radioactive Substances (Uranium and Thorium) Exemption Order 1962 

    E-Print Network [OSTI]

    Joseph, Keith

    1962-01-01

    STATUTORY INSTRUMENTS 1962 No.2710 ATOMIC ENERGY AND RADIOACTIVE SUBSTANCES The Radioactive Substances (Uranium and Thorium) Exemption Order 1962

  4. Plutonium recovery from spent reactor fuel by uranium displacement

    DOE Patents [OSTI]

    Ackerman, J.P.

    1992-03-17

    A process is described for separating uranium values and transuranic values from fission products containing rare earth values when the values are contained together in a molten chloride salt electrolyte. A molten chloride salt electrolyte with a first ratio of plutonium chloride to uranium chloride is contacted with both a solid cathode and an anode having values of uranium and fission products including plutonium. A voltage is applied across the anode and cathode electrolytically to transfer uranium and plutonium from the anode to the electrolyte while uranium values in the electrolyte electrolytically deposit as uranium metal on the solid cathode in an amount equal to the uranium and plutonium transferred from the anode causing the electrolyte to have a second ratio of plutonium chloride to uranium chloride. Then the solid cathode with the uranium metal deposited thereon is removed and molten cadmium having uranium dissolved therein is brought into contact with the electrolyte resulting in chemical transfer of plutonium values from the electrolyte to the molten cadmium and transfer of uranium values from the molten cadmium to the electrolyte until the first ratio of plutonium chloride to uranium chloride is reestablished.

  5. Uranium Mill Tailings Remedial Action Project surface project management plan

    SciTech Connect (OSTI)

    Not Available

    1994-09-01

    This Project Management Plan describes the planning, systems, and organization that shall be used to manage the Uranium Mill Tailings Remedial Action Project (UMTRA). US DOE is authorized to stabilize and control surface tailings and ground water contamination at 24 inactive uranium processing sites and associated vicinity properties containing uranium mill tailings and related residual radioactive materials.

  6. Soil to plant transfer of 238 Th on a uranium

    E-Print Network [OSTI]

    Hu, Qinhong "Max"

    Soil to plant transfer of 238 U, 226 Ra and 232 Th on a uranium mining-impacted soil from species grown in soils from southeastern China contaminated with uranium mine tailings were analyzed. Keywords: Uranium; Thorium; Radium; Tailings-contaminated soil; Soileplant transfer 1. Introduction

  7. Uranium Reduction in Sediments under Diffusion-Limited Transport of

    E-Print Network [OSTI]

    Hazen, Terry

    Uranium Reduction in Sediments under Diffusion-Limited Transport of Organic Carbon T E T S U K, Chicago, Illinois 60637 Costly disposal of uranium (U) contaminated sediments is motivating research. Introduction Uranium (U) is an important subsurface contaminant at sites associated with its mining

  8. Estimating terrestrial uranium and thorium by antineutrino flux measurements

    E-Print Network [OSTI]

    Mcdonough, William F.

    Estimating terrestrial uranium and thorium by antineutrino flux measurements Stephen T. Dye, and approved November 16, 2007 (received for review July 11, 2007) Uranium and thorium within the Earth produce of uranium and thorium concentrations in geological reservoirs relies largely on geochemi- cal model

  9. EPA Uranium Program Update Loren W. Setlow and

    E-Print Network [OSTI]

    EPA Uranium Program Update Loren W. Setlow and Reid J. Rosnick Environmental Protection Agency Office of Radiation and Indoor Air (6608J) Washington, DC 20460 NMA/NRC Uranium Recovery Workshop April 30, 2008 #12;2 Overview EPA Radiation protection program Uranium reports and abandoned mine lands

  10. Standard Review Plan for In Situ Leach Uranium

    E-Print Network [OSTI]

    NUREG-1569 Standard Review Plan for In Situ Leach Uranium Extraction License Applications Final Washington, DC 20555-0001 #12;NUREG-1569 Standard Review Plan for In Situ Leach Uranium Extraction License OF A STANDARD REVIEW PLAN (NUREG­1569) FOR STAFF REVIEWS FOR IN SITU LEACH URANIUM EXTRACTION LICENSE

  11. Plutonium recovery from spent reactor fuel by uranium displacement

    DOE Patents [OSTI]

    Ackerman, John P. (Downers Grove, IL)

    1992-01-01

    A process for separating uranium values and transuranic values from fission products containing rare earth values when the values are contained together in a molten chloride salt electrolyte. A molten chloride salt electrolyte with a first ratio of plutonium chloride to uranium chloride is contacted with both a solid cathode and an anode having values of uranium and fission products including plutonium. A voltage is applied across the anode and cathode electrolytically to transfer uranium and plutonium from the anode to the electrolyte while uranium values in the electrolyte electrolytically deposit as uranium metal on the solid cathode in an amount equal to the uranium and plutonium transferred from the anode causing the electrolyte to have a second ratio of plutonium chloride to uranium chloride. Then the solid cathode with the uranium metal deposited thereon is removed and molten cadmium having uranium dissolved therein is brought into contact with the electrolyte resulting in chemical transfer of plutonium values from the electrolyte to the molten cadmium and transfer of uranium values from the molten cadmium to the electrolyte until the first ratio of plutonium chloride to uranium chloride is reestablished.

  12. Appendix IV. Risks Associated with Conventional Uranium Milling Introduction

    E-Print Network [OSTI]

    as in situ leaching (ISL) mining operations, to provide a more complete picture of uranium production. While this report focuses on the impacts associated with conventional surface and underground uranium mines Radioactive Materials from Uranium Mining. Volume 1: Mining and Reclamation Background" by U.S. EPA (2006

  13. SANS Measurement of Hydrides in Uranium

    SciTech Connect (OSTI)

    Spooner, S; Ludtka, G.M.; Bullock, J.S.; Bridges, R.L.; Powell, G.L.

    2001-09-04

    SANS scattering is shown to be an effective method for detecting the presence of hydrogen precipitates in uranium. High purity polycrystalline samples of depleted uranium were given several hydriding treatments which included extended exposures to hydrogen gas at two different pressures at 630 C as well as a furnace anneal at 850 C followed by slow cooling in the near absence hydrogen gas. All samples exhibited neutron scattering that was in proportion to the expected levels of hydrogen content. While the scattering signal was strong, the shape of the scattering curve indicated that the scattering objects were large sized objects. Only by use of a very high angular resolution SANS technique was it possible to make estimates of the major diameter of the scattering objects. This analysis permits an estimate of the volume fraction and means size of the hydride precipitates in uranium.

  14. Method for fluorination of uranium oxide

    DOE Patents [OSTI]

    Petit, George S. (Oak Ridge, TN)

    1987-01-01

    Highly pure uranium hexafluoride is made from uranium oxide and fluorine. The uranium oxide, which includes UO.sub.3, UO.sub.2, U.sub.3 O.sub.8 and mixtures thereof, is introduced together with a small amount of a fluorine-reactive substance, selected from alkali chlorides, silicon dioxide, silicic acid, ferric oxide, and bromine, into a constant volume reaction zone. Sufficient fluorine is charged into the zone at a temperature below approximately 0.degree. C. to provide an initial pressure of at least approximately 600 lbs/sq. in. at the ambient atmospheric temperature. The temperature is then allowed to rise in the reaction zone until reaction occurs.

  15. Fission Enhanced diffusion of uranium in zirconia

    E-Print Network [OSTI]

    Bérerd, N; Moncoffre, N; Sainsot, P; Faust, H; Catalette, H

    2005-01-01

    This paper deals with the comparison between thermal and Fission Enhanced Diffusion (FED) of uranium into zirconia, representative of the inner face of cladding tubes. The experiments under irradiation are performed at the Institut Laue Langevin (ILL) in Grenoble using the Lohengrin spectrometer. A thin $^{235}UO\\_2$ layer in direct contact with an oxidized zirconium foil is irradiated in the ILL high flux reactor. The fission product flux is about 10$^{11}$ ions cm$^{-2}$ s$^{-1}$ and the target temperature is measured by an IR pyrometer. A model is proposed to deduce an apparent uranium diffusion coefficient in zirconia from the energy distribution broadening of two selected fission products. It is found to be equal to 10$^{-15}$ cm$^2$ s$^{-1}$ at 480$\\circ$C and compared to uranium thermal diffusion data in ZrO$\\_2$ in the same pressure and temperature conditions. The FED results are analysed in comparison with literature data.

  16. Aseismic design criteria for uranium enrichment plants

    SciTech Connect (OSTI)

    Beavers, J.E.

    1980-01-01

    In this paper technological, economical, and safety issues of aseismic design of uranium enrichment plants are presented. The role of management in the decision making process surrounding these issues is also discussed. The resolution of the issues and the decisions made by management are controlling factors in developing aseismic design criteria for any facility. Based on past experience in developing aseismic design criteria for the GCEP various recommendations are made for future enrichment facilities, and since uranium enrichment plants are members of the nuclear fuel cycle the discussion and recommendations presented herein are applicable to other nonreactor nuclear facilities.

  17. Simplifying strong electronic correlations in uranium: Localized uranium heavy-fermion UM2Zn20 (M=Co,Rh) compounds

    E-Print Network [OSTI]

    Lawrence, Jon

    Simplifying strong electronic correlations in uranium: Localized uranium heavy-fermion UM2Zn20 (M Atómica, 8400 Bariloche, Argentina 6 Department of Chemistry and Biochemistry, University of Delaware-field effects corroborate an ionic-like uranium electronic configura- tion in UM2Zn20. DOI: 10.1103/PhysRevB.78

  18. Steady State Sputtering Yields and Surface Compositions of Depleted Uranium and Uranium Carbide bombarded by 30 keV Gallium or 16 keV Cesium Ions.

    SciTech Connect (OSTI)

    Siekhaus, W. J.; Teslich, N. E.; Weber, P. K.

    2014-10-23

    Depleted uranium that included carbide inclusions was sputtered with 30-keV gallium ions or 16-kev cesium ions to depths much greater than the ions’ range, i.e. using steady-state sputtering. The recession of both the uranium’s and uranium carbide’s surfaces and the ion corresponding fluences were used to determine the steady-state target sputtering yields of both uranium and uranium carbide, i.e. 6.3 atoms of uranium and 2.4 units of uranium carbide eroded per gallium ion, and 9.9 uranium atoms and 3.65 units of uranium carbide eroded by cesium ions. The steady state surface composition resulting from the simultaneous gallium or cesium implantation and sputter-erosion of uranium and uranium carbide were calculated to be U??Ga??, (UC)??Ga?? and U??Cs?, (UC)??Cs??, respectively.

  19. EA-1495: Finding of No Significant Impact | Department of Energy

    Office of Environmental Management (EM)

    Publications EIS-0468: Final Environmental Impact Statement Advance Patent Waiver W(A)2012-021 Disposition of DOE Excess Depleted Uranium, Natural Uranium, and Low-Enriched Uranium...

  20. Securing the Sustainability of Global Medical Nuclear Supply Chains Through Economic Cost Recovery, Risk Management, and Optimization

    E-Print Network [OSTI]

    Nagurney, Anna

    of the radioisotope from highly enriched uranium targets to low enriched uranium targets. A case study for North of Molybdenum-99. The Molybde- num is produced by primarily irradiating Highly Enriched Uranium (HEU) targets

  1. The Uranium Institute 24th Annual Symposium

    E-Print Network [OSTI]

    Laughlin, Robert B.

    -239 for use in subsequent reactors. A fast neutron reactor is capable of producing more plutonium fuel than the uranium fuel it burns, leading to a breeder reactor. In addition, if the reactor is a fast with half lives of 30 years or less. The fast neutron reactor of preference was to be cooled with liquid

  2. The Quest for the Heaviest Uranium Isotope

    E-Print Network [OSTI]

    S. Schramm; D. Gridnev; D. V. Tarasov; V. N. Tarasov; W. Greiner

    2012-01-17

    We study Uranium isotopes and surrounding elements at very large neutron number excess. Relativistic mean field and Skyrme-type approaches with different parametrizations are used in the study. Most models show clear indications for isotopes that are stable with respect to neutron emission far beyond N=184 up to the range of around N=258.

  3. Standard test method for determination of uranium or gadolinium (or both) in gadolinium oxide-uranium oxide pellets or by X-ray fluorescence (XRF)

    E-Print Network [OSTI]

    American Society for Testing and Materials. Philadelphia

    2008-01-01

    Standard test method for determination of uranium or gadolinium (or both) in gadolinium oxide-uranium oxide pellets or by X-ray fluorescence (XRF)

  4. Quantifying Uranium Isotope Ratios Using Resonance Ionization Mass Spectrometry: The Influence of Laser Parameters on Relative Ionization Probability

    E-Print Network [OSTI]

    Isselhardt, Brett Hallen

    2011-01-01

    4.5 Uranium Isotope Ratio Measurements . . . . . .4.32 Uranium sputtered from three U-rich materials of varying uranium isotopic

  5. Control of structure and reactivity by ligand design : applications to small molecule activation by low-valent uranium complexes

    E-Print Network [OSTI]

    Lam, Oanh Phi

    2010-01-01

    of a Charge- Separated Uranium Benzophenone Ketyl Radical3. Charge-Separation in Uranium Diazomethane ComplexesRelated Small Molecules by Uranium Coordination Complexes”,

  6. Assessing the environmental availability of uranium in soils and sediments

    SciTech Connect (OSTI)

    Amonette, J.E.; Holdren, G.R. Jr.; Krupa, K.M.; Lindenmeier, C.W. [Pacific Northwest Lab., Richland, WA (United States)

    1994-06-01

    Soils and sediments contaminated with uranium pose certain environmental and ecological risks. At low to moderate levels of contamination, the magnitude of these risks depends not only on the absolute concentrations of uranium in the material but also on the availability of the uranium to drinking water supplies, plants, or higher organisms. Rational approaches for regulating the clean-up of sites contaminated with uranium, therefore, should consider the value of assessing the environmental availability of uranium at the site before making decisions regarding remediation. The purpose of this work is to review existing approaches and procedures to determine their potential applicability for assessing the environmental availability of uranium in bulk soils or sediments. In addition to making the recommendations regarding methodology, the authors have tabulated data from the literature on the aqueous complexes of uranium and major uranium minerals, examined the possibility of predicting environmental availability of uranium based on thermodynamic solubility data, and compiled a representative list of analytical laboratories capable of performing environmental analyses of uranium in soils and sediments.

  7. Fermentation and Hydrogen Metabolism Affect Uranium Reduction by Clostridia

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Gao, Weimin; Francis, Arokiasamy J.

    2013-01-01

    Previously, it has been shown that not only is uranium reduction under fermentation condition common among clostridia species, but also the strains differed in the extent of their capability and the pH of the culture significantly affected uranium(VI) reduction. In this study, using HPLC and GC techniques, metabolic properties of those clostridial strains active in uranium reduction under fermentation conditions have been characterized and their effects on capability variance of uranium reduction discussed. Then, the relationship between hydrogen metabolism and uranium reduction has been further explored and the important role played by hydrogenase in uranium(VI) and iron(III) reduction bymore »clostridia demonstrated. When hydrogen was provided as the headspace gas, uranium(VI) reduction occurred in the presence of whole cells of clostridia. This is in contrast to that of nitrogen as the headspace gas. Without clostridia cells, hydrogen alone could not result in uranium(VI) reduction. In alignment with this observation, it was also found that either copper(II) addition or iron depletion in the medium could compromise uranium reduction by clostridia. In the end, a comprehensive model was proposed to explain uranium reduction by clostridia and its relationship to the overall metabolism especially hydrogen (H 2 ) production. « less

  8. NNSA Partnership Successfully Removes All Remaining HEU from...

    National Nuclear Security Administration (NNSA)

    on nuclear and radiological security issues. NNSA worked with Uzbekistan's Institute of Nuclear Physics to convert its research reactor from HEU to low enriched uranium (LEU)...

  9. Y-12 fulfills major milestone in fuel conversion commitment for...

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

    The Y-12 National Security Complex recently fulfilled its commitment to provide low-enriched uranium as feedstock to fuel the "Safe LOW-POwer Kritical Experiment" (SLOWPOKE)...

  10. At DOE, nonproliferation sinks despite its success

    SciTech Connect (OSTI)

    Kramer, David

    2014-05-01

    Milestones are slipping for US efforts to round up vulnerable fissile materials and convert research reactors to low-enriched uranium.

  11. Quantification of the Potential Impact on Commercial Markets...

    Office of Environmental Management (EM)

    Introduction of the Enrichment Services Component of DOE Low Enriched Uranium Inventory During Calendar Year 2013 Quantification of the Potential Impact on Commercial Markets of...

  12. Uranium-Loaded Water Treatment Resins: 'Equivalent Feed' at NRC and Agreement State-Licensed Uranium Recovery Facilities - 12094

    SciTech Connect (OSTI)

    Camper, Larry W.; Michalak, Paul; Cohen, Stephen; Carter, Ted [Nuclear Regulatory Commission (United States)

    2012-07-01

    Community Water Systems (CWSs) are required to remove uranium from drinking water to meet EPA standards. Similarly, mining operations are required to remove uranium from their dewatering discharges to meet permitted surface water discharge limits. Ion exchange (IX) is the primary treatment strategy used by these operations, which loads uranium onto resin beads. Presently, uranium-loaded resin from CWSs and mining operations can be disposed as a waste product or processed by NRC- or Agreement State-licensed uranium recovery facilities if that licensed facility has applied for and received permission to process 'alternate feed'. The disposal of uranium-loaded resin is costly and the cost to amend a uranium recovery license to accept alternate feed can be a strong disincentive to commercial uranium recovery facilities. In response to this issue, the NRC issued a Regulatory Issue Summary (RIS) to clarify the agency's policy that uranium-loaded resin from CWSs and mining operations can be processed by NRC- or Agreement State-licensed uranium recovery facilities without the need for an alternate feed license amendment when these resins are essentially the same, chemically and physically, to resins that licensed uranium recovery facilities currently use (i.e., equivalent feed). NRC staff is clarifying its current alternate feed policy to declare IX resins as equivalent feed. This clarification is necessary to alleviate a regulatory and financial burden on facilities that filter uranium using IX resin, such as CWSs and mine dewatering operations. Disposing of those resins in a licensed facility could be 40 to 50 percent of the total operations and maintenance (O and M) cost for a CWS. Allowing uranium recovery facilities to treat these resins without requiring a license amendment lowers O and M costs and captures a valuable natural resource. (authors)

  13. The uranium cylinder assay system for enrichment plant safeguards

    SciTech Connect (OSTI)

    Miller, Karen A; Swinhoe, Martyn T; Marlow, Johnna B; Menlove, Howard O; Rael, Carlos D; Iwamoto, Tomonori; Tamura, Takayuki; Aiuchi, Syun

    2010-01-01

    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.

  14. In-line assay monitor for uranium hexafluoride

    DOE Patents [OSTI]

    Wallace, S.A.

    1980-03-21

    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 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 uranium-235. The uranium-235 content of the specimen is determined from comparison of the accumulated 185 keV energy counts and reference energy counts. The latter is used to measure the total uranium isotopic content of the specimen.

  15. Uranium accountancy in Atomic Vapor Laser Isotope Separation

    SciTech Connect (OSTI)

    Carver, R.D.

    1986-01-01

    The AVLIS program pioneers the large scale industrial application of lasers to produce low cost enriched uranium fuel for light water reactors. In the process developed at Lawrence Livermore National Laboratory, normal uranium is vaporized by an electron beam, and a precisely tuned laser beam selectively photo-ionizes the uranium-235 isotopes. These ions are moved in an electromagnetic field to be condensed on the product collector. All other uranium isotopes remain uncharged and pass through the collector section to condense as tails. Tracking the three types of uranium through the process presents special problems in accountancy. After demonstration runs, the uranium on the collector was analyzed for isotopic content by Battelle Pacific Northwest Laboratory. Their results were checked at LLNL by analysis of parallel samples. The differences in isotopic composition as reported by the two laboratories were not significant.

  16. Uranium enrichment management review: summary of analysis

    SciTech Connect (OSTI)

    Not Available

    1981-01-01

    In May 1980, the Assistant Secretary for Resource Applications within the Department of Energy requested that a group of experienced business executives be assembled to review the operation, financing, and management of the uranium enrichment enterprise as a basis for advising the Secretary of Energy. After extensive investigation, analysis, and discussion, the review group presented its findings and recommendations in a report on December 2, 1980. The following pages contain background material on which that final report was based. This report is arranged in chapters that parallel those of the uranium enrichment management review final report - chapters that contain summaries of the review group's discussion and analyses in six areas: management of operations and construction; long-range planning; marketing of enrichment services; financial management; research and development; and general management. Further information, in-depth analysis, and discussion of suggested alternative management practices are provided in five appendices.

  17. Assessment of Preferred Depleted Uranium Disposal Forms

    SciTech Connect (OSTI)

    Croff, A.G.; Hightower, J.R.; Lee, D.W.; Michaels, G.E.; Ranek, N.L.; Trabalka, J.R.

    2000-06-01

    The Department of Energy (DOE) is in the process of converting about 700,000 metric tons (MT) of depleted uranium hexafluoride (DUF6) containing 475,000 MT of depleted uranium (DU) to a stable form more suitable for long-term storage or disposal. Potential conversion forms include the tetrafluoride (DUF4), oxide (DUO2 or DU3O8), or metal. If worthwhile beneficial uses cannot be found for the DU product form, it will be sent to an appropriate site for disposal. The DU products are considered to be low-level waste (LLW) under both DOE orders and Nuclear Regulatory Commission (NRC) regulations. The objective of this study was to assess the acceptability of the potential DU conversion products at potential LLW disposal sites to provide a basis for DOE decisions on the preferred DU product form and a path forward that will ensure reliable and efficient disposal.

  18. Uranium Oxide Aerosol Transport in Porous Graphite

    SciTech Connect (OSTI)

    Blanchard, Jeremy; Gerlach, David C.; Scheele, Randall D.; Stewart, Mark L.; Reid, Bruce D.; Gauglitz, Phillip A.; Bagaasen, Larry M.; Brown, Charles C.; Iovin, Cristian; Delegard, Calvin H.; Zelenyuk, Alla; Buck, Edgar C.; Riley, Brian J.; Burns, Carolyn A.

    2012-01-23

    The objective of this paper is to investigate the transport of uranium oxide particles that may be present in carbon dioxide (CO2) gas coolant, into the graphite blocks of gas-cooled, graphite moderated reactors. The transport of uranium oxide in the coolant system, and subsequent deposition of this material in the graphite, of such reactors is of interest because it has the potential to influence the application of the Graphite Isotope Ratio Method (GIRM). The GIRM is a technology that has been developed to validate the declared operation of graphite moderated reactors. GIRM exploits isotopic ratio changes that occur in the impurity elements present in the graphite to infer cumulative exposure and hence the reactor’s lifetime cumulative plutonium production. Reference Gesh, et. al., for a more complete discussion on the GIRM technology.

  19. Engineering assessment of inactive uranium mill tailings

    SciTech Connect (OSTI)

    Not Available

    1981-07-01

    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.

  20. Fayans functional for deformed nuclei. Uranium region

    E-Print Network [OSTI]

    S. V. Tolokonnikov; I. N. Borzov; M. Kortelainen; Yu. S. Lutostansky; E. E. Saperstein

    2015-08-03

    Fayans energy density functional (EDF) FaNDF^0 has been applied to the nuclei around uranium region. Ground state characteristics of the Th, U and Pu isotopic chains, up to the two-neutron drip line, are found and compared with predictions from several Skyrme EDFs. The two-neutron drip line is found for FaNDF^0, SLy4 and SkM^* EDFs for a set of elements with even proton number, from Pb up to Fm.

  1. Fayans functional for deformed nuclei. Uranium region

    E-Print Network [OSTI]

    Tolokonnikov, S V; Kortelainen, M; Lutostansky, Yu S; Saperstein, E E

    2015-01-01

    Fayans energy density functional (EDF) FaNDF^0 has been applied to the nuclei around uranium region. Ground state characteristics of the Th, U and Pu isotopic chains, up to the two-neutron drip line, are found and compared with predictions from several Skyrme EDFs. The two-neutron drip line is found for FaNDF^0, SLy4 and SkM^* EDFs for a set of elements with even proton number, from Pb up to Fm.

  2. Incorporation of oxidized uranium into Fe (hydr)oxides during Fe(II) catalyzed remineralization

    E-Print Network [OSTI]

    Nico, Peter S.

    2010-01-01

    Uranium isotopic evidence for the origin of the Bahariya iron deposits,U deposit, and the DOE Oak Ridge site (where uranium bearingdeposits, mining activities, and nuclear weapons production. Uranium

  3. Magnetic Exchange Coupling and Single-Molecule Magnetism in Uranium Complexes

    E-Print Network [OSTI]

    Rinehart, Jeffrey Dennis

    2010-01-01

    in molecular uranium cluster chemistry. 13 Compound 2 ischemistry and small-molecule reactivity of uranium. AmongUranium Complexes by Jeffrey Dennis Rinehart Doctor of Philosophy in Chemistry

  4. Recent International R&D Activities in the Extraction of Uranium from Seawater

    E-Print Network [OSTI]

    Rao, Linfeng

    2011-01-01

    Uranium and Rare Earth Elements Using Biomass of Algae, Bioinorganic Chemistry andRecovery of uranium from sea water. Chemistry & Industry (of uranium from seawater. Turkish Journal of Chemistry, 17 (

  5. CRYSTAL AND MOLECULAR STRUCTURE OF HYDRIDOTIS (BIS(TRIMETHYLSILYL)AMIDO]URANIUM(IV)

    E-Print Network [OSTI]

    Andersen, Richard A.

    2012-01-01

    BIS(TRIMETHYLSILYL)AMIDO]URANIUM(IV) Richard A. Andersen,BIS(TRIMETHYLSILYL)AMIDO]URANIUM(IV) Richard A. Andersen,of thorium (IV) and uranium (IV), HM[N(SiMe ) 2] 3 , have

  6. Examination of Uranium(VI) Leaching During Ligand Promoted Dissolution of Waste Tank Sludge Surrogates

    E-Print Network [OSTI]

    Powell, Brian A.

    2008-01-01

    Effects of phosphate on uranium(VI) adsorption to goethite-and ionic strength upon uranium(VI) sorption onto alumina asD. R. , Leslie, B. W. , Uranium sorption on a-alumina:

  7. Investigation of the electronic structure of mono(1,1?- diamidoferrocene) uranium(IV) complexes

    E-Print Network [OSTI]

    Duhovi?, S; Oria, JV; Odoh, SO; Schreckenbach, G; Batista, ER; Diaconescu, PL

    2013-01-01

    1,1’- Diamidoferrocene) Uranium(IV) Complexes Selma Duhovi?,mono(1,1’- diamidoferrocene) uranium complexes (NN R )UX 2 (as actinides. 17-19 For uranium, we have observed a wide

  8. Uranium Recovery from Seawater: Development of Fiber Adsorbents Prepared via Atom-Transfer Radical Polymerization

    SciTech Connect (OSTI)

    Saito, Tomonori; Brown, Suree; Chatterjee, Sabornie; Kim, Jungseung; Tsouris, Constantinos; Mayes, Richard; Kuo, Li-Jung; Gill, Gary A.; Oyola, Yatsandra; Janke, C.; Dai, Sheng

    2014-07-09

    Uranium exists uniformly at a concentration of ~3.3 ppb in seawater. The extraction of uranium from seawater presents a very attractive alternative source of uranium for nuclear fuel needs.

  9. The US uranium industry: Regulatory and policy impediments

    SciTech Connect (OSTI)

    Drennen, T.E.; Glicken, J.

    1995-06-01

    The Energy Policy Act of 1992 required the DOE to develop recommendations and implement government programs to assist the domestic uranium industry in increasing export opportunities. In 1993, as part of that effort, the Office of Nuclear Energy identified several key factors that could (or have) significantly impact(ed) export opportunities for domestic uranium. This report addresses one of these factors: regulatory and policy impediments to the flow of uranium products between the US and other countries. It speaks primarily to the uranium market for civil nuclear power. Changes in the world political and economic order have changed US national security requirements, and the US uranium industry has found itself without the protected market it once enjoyed. An unlevel playing field for US uranium producers has resulted from a combination of geology, history, and a general US political philosophy of nonintervention that precludes the type of industrial policy practiced in other uranium-exporting countries. The US has also been hampered in its efforts to support the domestic uranium-producing industry by its own commitment to free and open global markets and by international agreements such as GATT and NAFTA. Several US policies, including the imposition of NRC fees and licensing costs and Harbor Maintenance fees, directly harm the competitiveness of the domestic uranium industry. Finally, requirements under US law, such as those in the 1979 Nuclear Nonproliferation Act, place very strict limits on the use of US-origin uranium, limitations not imposed by other uranium-producing countries. Export promotion and coordination are two areas in which the US can help the domestic uranium industry without violating existing trade agreements or other legal or policy constraints.

  10. Colloids generation from metallic uranium fuel

    SciTech Connect (OSTI)

    Metz, C.; Fortner, J.; Goldberg, M.; Shelton-Davis, C.

    2000-07-20

    The possibility of colloid generation from spent fuel in an unsaturated environment has significant implications for storage of these fuels in the proposed repository at Yucca Mountain. Because colloids can act as a transport medium for sparingly soluble radionuclides, it might be possible for colloid-associated radionuclides to migrate large distances underground and present a human health concern. This study examines the nature of colloidal materials produced during corrosion of metallic uranium fuel in simulated groundwater at elevated temperature in an unsaturated environment. Colloidal analyses of the leachates from these corrosion tests were performed using dynamic light scattering and transmission electron microscopy. Results from both techniques indicate a bimodal distribution of small discrete particles and aggregates of the small particles. The average diameters of the small, discrete colloids are {approximately}3--12 nm, and the large aggregates have average diameters of {approximately}100--200 nm. X-ray diffraction of the solids from these tests indicates a mineral composition of uranium oxide or uranium oxy-hydroxide.

  11. Equation of State of Uranium and Plutonium

    E-Print Network [OSTI]

    Barroso, Dalton Ellery Girão

    2015-01-01

    The objective of this work is to define the parameters of the three-term equation of state for uranium and plutonium, appropriate for conditions in which these materials are subjected to strong shock compressions, as in cylindrical and spherical implosions. The three-term equation of state takes into account the three components of the pressure that resist to compression in the solid: the elastic or "cold" pressure (coulombian repulsion between atoms), the thermal pressure due to vibratory motion of atoms in the lattice of the solid and the thermal pressure of electrons thermally excited. The equation of state defined here permits also to take into account the variation of the specific heat with the transition of the solid to the liquid or gaseous state due to continued growth of temperature in strong shock compressions. In the definition of uranium equation of state, experimental data on the uranium compression, available in the open scientific literature, are used. In the plutonium case, this element was co...

  12. Equation of State of Uranium and Plutonium

    E-Print Network [OSTI]

    Dalton Ellery Girão Barroso

    2015-07-13

    The objective of this work is to define the parameters of the three-term equation of state for uranium and plutonium, appropriate for conditions in which these materials are subjected to strong shock compressions, as in cylindrical and spherical implosions. The three-term equation of state takes into account the three components of the pressure that resist to compression in the solid: the elastic or "cold" pressure (coulombian repulsion between atoms), the thermal pressure due to vibratory motion of atoms in the lattice of the solid and the thermal pressure of electrons thermally excited. The equation of state defined here permits also to take into account the variation of the specific heat with the transition of the solid to the liquid or gaseous state due to continued growth of temperature in strong shock compressions. In the definition of uranium equation of state, experimental data on the uranium compression, available in the open scientific literature, are used. In the plutonium case, this element was considered initially in the alpha-phase or stabilized in the delta-phase. In the last case, an abrupt and instantaneous transition to the alpha-phase was considered when the delta-phase plutonium is submitted to strong compressions.

  13. Supply of enriched uranium for research reactors

    SciTech Connect (OSTI)

    Mueller, H. [NUKEM GmbH, Alzenau (Germany)

    1997-08-01

    Since the RERTR-meeting In Newport/USA in 1990 the author delivered a series of papers in connection with the fuel cycle for research reactors dealing with its front-end. In these papers the author underlined the need for unified specifications for enriched uranium metal suitable for the production of fuel elements and made proposals with regard to the re-use of in Europe reprocessed highly enriched uranium. With regard to the fuel cycle of research reactors the research reactor community was since 1989 more concentrating on the problems of its back-end since the USA stopped the acceptance of spent research reactor fuel on December 31, 1988. Now, since it is apparent that these back-end problem have been solved by AEA`s ability to reprocess and the preparedness of the USA to again accept physically spent research reactor fuel the author is focusing with this paper again on the front-end of the fuel cycle on the question whether there is at all a safe supply of low and high enriched uranium for research reactors in the future.

  14. Chapter 3. Volume and Characteristics of Uranium Mine Wastes Uranium has been found and mined in a wide variety of rocks, including sandstone, carbonates1

    E-Print Network [OSTI]

    3-1 Chapter 3. Volume and Characteristics of Uranium Mine Wastes Uranium has been found and mined conventional mining, solution extraction, and milling of uranium, a principal focus of this report is TENORM, or which may need future reclamation. When uranium mining first started, most of the ores were recovered

  15. Uranium from Seawater Program Review; Fuel Resources Uranium from Seawater Program DOE Office of Nuclear Energy

    SciTech Connect (OSTI)

    2013-07-01

    For nuclear energy to remain sustainable in the United States, economically viable sources of uranium beyond terrestrial ores must be developed. The goal of this program is to develop advanced adsorbents that can extract uranium from seawater at twice the capacity of the best adsorbent developed by researchers at the Japan Atomic Energy Agency (JAEA), 1.5 mg U/g adsorbent. A multidisciplinary team from Oak Ridge National Laboratory, Lawrence Berkeley National Laboratory, Pacific Northwest National Laboratory, and the University of Texas at Austin was assembled to address this challenging problem. Polymeric adsorbents, based on the radiation grafting of acrylonitrile and methacrylic acid onto high surface-area polyethylene fibers followed by conversion of the nitriles to amidoximes, have been developed. These poly(acrylamidoxime-co-methacrylic acid) fibers showed uranium adsorption capacities for the extraction of uranium from seawater that exceed 3 mg U/g adsorbent in testing at the Pacific Northwest National Laboratory Marine Sciences Laboratory. The essence of this novel technology lies in the unique high surface-area trunk material that considerably increases the grafting yield of functional groups without compromising its mechanical properties. This technology received an R&D100 Award in 2012. In addition, high surface area nanomaterial adsorbents are under development with the goal of increasing uranium adsorption capacity by taking advantage of the high surface areas and tunable porosity of carbon-based nanomaterials. Simultaneously, de novo structure-based computational design methods are being used to design more selective and stable ligands and the most promising candidates are being synthesized, tested and evaluated for incorporation onto a support matrix. Fundamental thermodynamic and kinetic studies are being carried out to improve the adsorption efficiency, the selectivity of uranium over other metals, and the stability of the adsorbents. Understanding the rate-limiting step of uranium uptake from seawater is also essential in designing an effective uranium recovery system. Finally, economic analyses have been used to guide these studies and highlight what parameters, such as capacity, recyclability, and stability, have the largest impact on the cost of extraction of uranium from seawater. Initially, the cost estimates by the JAEA for extraction of uranium from seawater with braided polymeric fibers functionalized with amidoxime ligands were evaluated and updated. The economic analyses were subsequently updated to reflect the results of this project while providing insight for cost reductions in the adsorbent development through “cradle-to-grave” case studies for the extraction process. This report highlights the progress made over the last three years on the design, synthesis, and testing of new materials to extract uranium for seawater. This report is organized into sections that highlight the major research activities in this project: (1) Chelate Design and Modeling, (2) Thermodynamics, Kinetics and Structure, (3) Advanced Polymeric Adsorbents by Radiation Induced Grafting, (4) Advanced Nanomaterial Adsorbents, (5) Adsorbent Screening and Modeling, (6) Marine Testing, and (7) Cost and Energy Assessment. At the end of each section, future research directions are briefly discussed to highlight the challenges that still remain to reduce the cost of extractions of uranium for seawater. Finally, contributions from the Nuclear Energy University Programs (NEUP), which complement this research program, are included at the end of this report.

  16. The radioactive Substances (Prepared Uranium Thorium Compounds) Exemption Order 1962 

    E-Print Network [OSTI]

    Joseph, Keith

    1962-01-01

    STATUTORY INSTRUMENTS 1962 No. 2711 ATOMIC ENERGY AND RADIOACI1VE SUBSTANCES The Radioactive Substances (prepared Uranium and Thorium Compounds) Exemption Order 1962

  17. High grade uranium resources in the United States : an overview

    E-Print Network [OSTI]

    Graves, Richard E.

    1974-01-01

    A time analysis of uranium exploration, production and known reserves in the United States is employed to reveal industry trends. The

  18. The Hydrogen Corrosion of Uranium: Identification of Underlying...

    Office of Scientific and Technical Information (OSTI)

    The Hydrogen Corrosion of Uranium: Identification of Underlying Causes and Proposed Mitigation Strategies Citation Details In-Document Search Title: The Hydrogen Corrosion of...

  19. Degradation problems with the solvent extraction organic at Roessing uranium

    SciTech Connect (OSTI)

    Munyungano, Brodrick; Feather, Angus; Virnig, Michael

    2008-07-01

    Roessing Uranium Ltd recovers uranium from a low-grade ore in Namibia. Uranium is recovered and purified from an ion-exchange eluate in a solvent-extraction plant. The solvent-extraction plant uses Alamine 336 as the extractant for uranium, with isodecanol used as a phase modifier in Sasol SSX 210, an aliphatic hydrocarbon diluent. Since the plant started in the mid 1970's, there have been a few episodes where the tertiary amine has been quickly and severely degraded when the plant was operated outside certain operating parameters. The Rossing experience is discussed in more detail in this paper. (authors)

  20. Basic characterization of highly enriched uranium by gamma spectrometry

    E-Print Network [OSTI]

    Cong Tam Nguyen; Jozsef Zsigrai

    2005-08-25

    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.

  1. Basic characterization of highly enriched uranium by gamma spectrometry

    E-Print Network [OSTI]

    Nguyen, C T

    2006-01-01

    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.

  2. EIS-0359: Uranium Hexafluoride Conversion Facility at the Paducah...

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

    and decontamination and decommissioning of the proposed depleted uranium hexafluoride (DUF6) conversion facility at three locations within the Paducah site; transportation of...

  3. EIS-0360: Depleted Uranium Oxide Conversion Product at the Portsmouth...

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

    and decontamination and decommissioning of the proposed depleted uranium hexafluoride (DUF6) conversion facility at three alternative locations within the Portsmouth site;...

  4. DOE Evaluates Environmental Impacts of Uranium Mining on Government...

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

    JUNCTION, Colo. - The U.S. Department of Energy (DOE) today announced that the Final Uranium Leasing Program Programmatic Environmental Impact Statement (PEIS) is available to...

  5. Uranium and Strontium Batch Sorption and Diffusion Kinetics into...

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

    Uranium and Strontium Batch Sorption and Diffusion Kinetics into Mesoporous Silica Friday, February 27, 2015 Figure 1 Figure 1. Transmission electron microscopy images of (A)...

  6. Abandoned Uranium Mine Technical Services and Cleanup Industry...

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

    Abandoned Uranium Mine Technical Services and Cleanup Industry Day In January 2015, the United States (U.S.) and the Anadarko Litigation Trust ("Litigation Trust") entered into a...

  7. Electrochemical method of producing eutectic uranium alloy and apparatus

    DOE Patents [OSTI]

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

    1995-01-10

    An apparatus and method are disclosed for continuous production of liquid uranium alloys through the electrolytic reduction of uranium chlorides. The apparatus includes an electrochemical cell formed from an anode shaped to form an electrolyte reservoir, a cathode comprising a metal, such as iron, capable of forming a eutectic uranium alloy having a melting point less than the melting point of pure uranium, and molten electrolyte in the reservoir comprising a chlorine or fluorine containing salt and uranium chloride. The method of the invention produces an eutectic uranium alloy by creating an electrolyte reservoir defined by a container comprising an anode, placing an electrolyte in the reservoir, the electrolyte comprising a chlorine or fluorine containing salt and uranium chloride in molten form, positioning a cathode in the reservoir where the cathode comprises a metal capable of forming an uranium alloy having a melting point less than the melting point of pure uranium, and applying a current between the cathode and the anode. 2 figures.

  8. Toxic Substances Control Act Uranium Enrichment Federal Facilities...

    Office of Environmental Management (EM)

    Toxic Substance Control Act Uranium Enrichment Federal Facilities Compliance Agreement (TSCA-UE- FFCA), February 20, 1992 State Kentucky Agreement Type Compliance Agreement Legal...

  9. The Uranium Processing Facility Finite Element Meshing Discussion

    Office of Environmental Management (EM)

    Uranium Processing Facility (UPF) Finite Element Meshing Discussion ...Need picture of Building... October 25, 2011 Department of Energy - Natural Phenomenon Hazard Workshop 1...

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

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

    440 Highly Enriched Uranium Materials Facility (HEUMF) Major Design Changes Late Lessons Learned Report Apr 2010.pdf More Documents & Publications EIS-0387: Draft Site-Wide...

  11. Toxic Substances Control Act Uranium Enrichment Federal Facilities...

    Office of Environmental Management (EM)

    Toxic Substance Control Act Uranium Enrichment Federal Facilities Compliance Agreement (TSCA-UE- FFCA), February 20, 1992 State Ohio Agreement Type Compliance Agreement Legal...

  12. Method of fabricating a uranium-bearing foil

    DOE Patents [OSTI]

    Gooch, Jackie G. (Seymour, TN); DeMint, Amy L. (Kingston, TN)

    2012-04-24

    Methods of fabricating a uranium-bearing foil are described. The foil may be substantially pure uranium, or may be a uranium alloy such as a uranium-molybdenum alloy. The method typically includes a series of hot rolling operations on a cast plate material to form a thin sheet. These hot rolling operations are typically performed using a process where each pass reduces the thickness of the plate by a substantially constant percentage. The sheet is typically then annealed and then cooled. The process typically concludes with a series of cold rolling passes where each pass reduces the thickness of the plate by a substantially constant thickness amount to form the foil.

  13. President Truman Increases Production of Uranium and Plutonium...

    National Nuclear Security Administration (NNSA)

    Increases Production of Uranium and Plutonium | National Nuclear Security Administration Facebook Twitter Youtube Flickr RSS People Mission Managing the Stockpile Preventing...

  14. Promoting Uranium Immobilization by the Activities of Microbial...

    Office of Scientific and Technical Information (OSTI)

    of uranium U(VI) phosphate precipitates. Specifically, we hypothesize that the precipitation of U(VI) phosphate minerals may be promoted through the microbial release andor...

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

    SciTech Connect (OSTI)

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

    1993-02-01

    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.

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

    SciTech Connect (OSTI)

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

    1993-02-01

    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.

  17. Reaction of uranium oxides with chlorine and carbon or carbon monoxide to prepare uranium chlorides

    SciTech Connect (OSTI)

    Haas, P.A.; Lee, D.D.; Mailen, J.C.

    1991-11-01

    The preferred preparation concept of uranium metal for feed to an AVLIS uranium enrichment process requires preparation of uranium tetrachloride (UCI{sub 4}) by reacting uranium oxides (UO{sub 2}/UO{sub 3}) and chlorine (Cl{sub 2}) in a molten chloride salt medium. UO{sub 2} is a very stable metal oxide; thus, the chemical conversion requires both a chlorinating agent and a reducing agent that gives an oxide product which is much more stable than the corresponding chloride. Experimental studies in a quartz reactor of 4-cm ID have demonstrated the practically of some chemical flow sheets. Experimentation has illustrated a sequence of results concerning the chemical flow sheets. Tests with a graphite block at 850{degrees}C demonstrated rapid reactions of Cl{sub 2} and evolution of carbon dioxide (CO{sub 2}) as a product. Use of carbon monoxide (CO) as the reducing agent also gave rapid reactions of Cl{sub 2} and formation of CO{sub 2} at lower temperatures, but the reduction reactions were slower than the chlorinations. Carbon powder in the molten salt melt gave higher rates of reduction and better steady state utilization of Cl{sub 2}. Addition of UO{sub 2} feed while chlorination was in progress greatly improved the operation by avoiding the plugging effects from high UO{sub 2} concentrations and the poor Cl{sub 2} utilizations from low UO{sub 2} concentrations. An UO{sub 3} feed gave undesirable effects while a feed of UO{sub 2}-C spheres was excellent. The UO{sub 2}-C spheres also gave good rates of reaction as a fixed bed without any molten chloride salt. Results with a larger reactor and a bottom condenser for volatilized uranium show collection of condensed uranium chlorides as a loose powder and chlorine utilizations of 95--98% at high feed rates. 14 refs., 7 figs., 14 tabs.

  18. Stratigraphy of the PB-1 well, Nopal I uranium deposit, Sierra Pena Blanca, Chihuahua, Mexico

    E-Print Network [OSTI]

    Dobson, P.

    2009-01-01

    and geochronology of the Nopal I uranium deposit, Mexico:with hydrothermally altered Nopal Formation rhyolitic tuff.uranium mineralization at the Nopal deposit include Calas (

  19. CRYSTAL AND MOLECULAR STRUCTURE OF HYDRIDOTIS (BIS(TRIMETHYLSILYL)AMIDO]URANIUM(IV)

    E-Print Network [OSTI]

    Andersen, Richard A.

    2012-01-01

    Chemistry University of California Berkeley, California 94720 New hydride derivatives of thorium (IV) and uranium (Chemistry CRYSTAL AND MOLECULAR STRUCTURE OF HYDRIDOTRIS[BIS(TRIMETHYLSILYL)AMIDO]URANIUM(

  20. Novel Transformations using Uranium and Group 5 Metal Complexes Supported by 1,1'-diamidoferrocene Ligands

    E-Print Network [OSTI]

    Lopez, Michael Joseph

    2013-01-01

    chemistry has grown significantly in the past decade. 1 UraniumChemistry by Michael Joseph Lopez ABSTRACT OF THE THESIS Novel Transformations using Uranium

  1. Inherently safe in situ uranium recovery (Patent) | SciTech Connect

    Office of Scientific and Technical Information (OSTI)

    Inherently safe in situ uranium recovery Citation Details In-Document Search Title: Inherently safe in situ uranium recovery You are accessing a document from the Department of...

  2. DOE Announces Transfer of Depleted Uranium to Advance the U.S...

    Energy Savers [EERE]

    Transfer of Depleted Uranium to Advance the U.S. National Security Interests, Extend Operations at Paducah Gaseous Diffusion Plant DOE Announces Transfer of Depleted Uranium to...

  3. Recent International R&D Activities in the Extraction of Uranium from Seawater

    E-Print Network [OSTI]

    Rao, Linfeng

    2011-01-01

    Poletiko, S. Prabhakar, P. K. Tewari, Extraction of uranium1982) 145-150. 27. P. K. Tewari, Recovery of Uranium from

  4. Process for recovering uranium from waste hydrocarbon oils containing the same. [Uranium contaminated lubricating oils from gaseous diffusion compressors

    DOE Patents [OSTI]

    Conrad, M.C.; Getz, P.A.; Hickman, J.E.; Payne, L.D.

    1982-06-29

    The invention is a process for the recovery of uranium from uranium-bearing hydrocarbon oils containing carboxylic acid as a degradation product. In one aspect, the invention comprises providing an emulsion of water and the oil, heating the same to a temperature effecting conversion of the emulsion to an organic phase and to an acidic aqueous phase containing uranium carboxylate, and recovering the uranium from the aqueous phase. The process is effective, simple and comparatively inexpensive. It avoids the use of toxic reagents and the formation of undesirable intermediates.

  5. Development of Novel Sorbents for Uranium Extraction from Seawater

    SciTech Connect (OSTI)

    Lin, Wenbin; Taylor-Pashow, Kathryn

    2014-01-08

    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.

  6. Uranium isotopes in ground water as a prospecting technique

    SciTech Connect (OSTI)

    Cowart, J.B.; Osmond, J.K.

    1980-02-01

    The isotopic concentrations of dissolved uranium were determined for 300 ground water samples near eight known uranium accumulations to see if new approaches to prospecting could be developed. It is concluded that a plot of /sup 234/U//sup 238/U activity ratio (A.R.) versus uranium concentration (C) can be used to identify redox fronts, to locate uranium accumulations, and to determine whether such accumulations are being augmented or depleted by contemporary aquifer/ground water conditions. In aquifers exhibiting flow-through hydrologic systems, up-dip ground water samples are characterized by high uranium concentration values (> 1 to 4 ppB) and down-dip samples by low uranium concentration values (less than 1 ppB). The boundary between these two regimes can usually be identified as a redox front on the basis of regional water chemistry and known uranium accumulations. Close proximity to uranium accumulations is usually indicated either by very high uranium concentrations in the ground water or by a combination of high concentration and high activity ratio values. Ground waters down-dip from such accumulations often exhibit low uranium concentration values but retain their high A.R. values. This serves as a regional indicator of possible uranium accumulations where conditions favor the continued augmentation of the deposit by precipitation from ground water. Where the accumulation is being dispersed and depleted by the ground water system, low A.R. values are observed. Results from the Gulf Coast District of Texas and the Wyoming districts are presented.

  7. Mixed uranium dicarbide and uranium dioxide microspheres and process of making same

    DOE Patents [OSTI]

    Stinton, David P. (Knoxville, TN)

    1983-01-01

    Nuclear fuel microspheres are made by sintering microspheres containing uranium dioxide and uncombined carbon in a 1 mole percent carbon monoxide/99 mole percent argon atmosphere at 1550.degree. C. and then sintering the microspheres in a 3 mole percent carbon monoxide/97 mole percent argon atmosphere at the same temperature.

  8. Spectroscopic Evidence for Uranium Bearing Precipitates in Vadose Zone

    E-Print Network [OSTI]

    of past nuclear fuel fabrication processes, uranium (U) has been recognized as one of the most widespreadHanfordsitesthatreceivedU-containingwastesduring its mission of Pu production between 1940 and 1990. Unirradiated fuel rod wastes were disposed to the 300 Area that included copper-uranium-nitric acid solutions and dissolved aluminum cladding (basic

  9. Uranium and cesium diffusion in fuel cladding of electrogenerating channel

    SciTech Connect (OSTI)

    Vasil’ev, I. V. Ivanov, A. S.; Churin, V. A.

    2014-12-15

    The results of reactor tests of a carbonitride fuel in a single-crystal cladding from a molybdenum-based alloy can be used in substantiating the operational reliability of fuels in developing a project of a megawatt space nuclear power plant. The results of experimental studies of uranium and cesium penetration into the single-crystal cladding of fuel elements with a carbonitride fuel are interpreted. Those fuel elements passed nuclear power tests in the Ya-82 pilot plant for 8300 h at a temperature of about 1500°C. It is shown that the diffusion coefficients for uranium diffusion into the cladding are virtually coincident with the diffusion coefficients measured earlier for uranium diffusion into polycrystalline molybdenum. It is found that the penetration of uranium into the cladding is likely to occur only in the case of a direct contact between the cladding and fuel. The experimentally observed nonmonotonic uranium-concentration profiles are explained in terms of predominant uranium diffusion along grain boundaries. It is shown that a substantially nonmonotonic behavior observed in our experiment for the uranium-concentration profile may be explained by the presence of a polycrystalline structure of the cladding in the surface region from its inner side. The diffusion coefficient is estimated for the grain-boundary diffusion of uranium. The diffusion coefficients for cesium are estimated on the basis of experimental data obtained in the present study.

  10. Case Study/ Effects of Groundwater Development on Uranium

    E-Print Network [OSTI]

    Case Study/ Effects of Groundwater Development on Uranium: Central Valley, California, USA Abstract Uranium (U) concentrations in groundwater in several parts of the eastern San Joaquin Valley development during the last 100 years have changed the chemistry and magnitude of groundwater recharge

  11. Adsorption study for uranium in Rocky Flats groundwater

    SciTech Connect (OSTI)

    Laul, J.C.; Rupert, M.C.; Harris, M.J.; Duran, A.

    1995-01-01

    Six adsorbents were studied to determine their effectiveness in removing uranium in Rocky Flats groundwater. The bench column and batch (Kd) tests showed that uranium can be removed (>99.9%) by four adsorbents. Bone Charcoal (R1O22); F-1 Alumina (granular activated alumina); BIOFIX (immobilized biological agent); SOPBPLUS (mixed metal oxide); Filtrasorb 300 (granular activated carbon); and Zeolite (clinoptilolite).

  12. Uranium in US surface, ground, and domestic waters. Volume 2

    SciTech Connect (OSTI)

    Drury, J.S.; Reynolds, S.; Owen, P.T.; Ross, R.H.; Ensminger, J.T.

    1981-04-01

    The report Uranium in US Surface, Ground, and Domestic Waters comprises four volumes. Volumes 2, 3, and 4 contain data characterizing the location, sampling date, type, use, and uranium conentrations of 89,994 individual samples presented in tabular form. The tabular data in volumes 2, 3, and 4 are summarized in volume 1 in narrative form and with maps and histograms.

  13. Uranium in US surface, ground, and domestic waters

    SciTech Connect (OSTI)

    Drury, J.S.; Reynolds, S.; Owen, P.T.; Ross, R.H.; Ensminger, J.T.

    1981-04-01

    The report Uranium in US Surface, Ground, and Domestic Waters comprises four volumes. Volumes 2, 3, and 4 contain data characterizing the location, sampling date, type, use, and uranium concentrations of 89,994 individual samples presented in tabular form. The tabular data in volumes 2, 3, and 4 are summarized in volume 1 in narrative form and with maps and histograms.

  14. Preserving Ultra-Pure Uranium-233

    SciTech Connect (OSTI)

    Krichinsky, Alan M [ORNL; Goldberg, Dr. Steven A. [DOE SC - Chicago Office; Hutcheon, Dr. Ian D. [Lawrence Livermore National Laboratory (LLNL)

    2011-10-01

    Uranium-233 ({sup 233}U) is a synthetic isotope of uranium formed under reactor conditions during neutron capture by natural thorium ({sup 232}Th). At high purities, this synthetic isotope serves as a crucial reference material for accurately quantifying and characterizing uranium-bearing materials assays and isotopic distributions for domestic and international nuclear safeguards. Separated, high purity {sup 233}U is stored in vaults at Oak Ridge National Laboratory (ORNL). These materials represent a broad spectrum of {sup 233}U from the standpoint of isotopic purity - the purest being crucial for precise analyses in safeguarding uranium. All {sup 233}U at ORNL is currently scheduled to be disposed of by down-blending with depleted uranium beginning in 2015. This will reduce safety concerns and security costs associated with storage. Down-blending this material will permanently destroy its potential value as a certified reference material for use in uranium analyses. Furthermore, no credible options exist for replacing {sup 233}U due to the lack of operating production capability and the high cost of restarting currently shut down capabilities. A study was commissioned to determine the need for preserving high-purity {sup 233}U. This study looked at the current supply and the historical and continuing domestic need for this crucial isotope. It examined the gap in supplies and uses to meet domestic needs and extrapolated them in the context of international safeguards and security activities - superimposed on the recognition that existing supplies are being depleted while candidate replacement material is being prepared for disposal. This study found that the total worldwide need by this projection is at least 850 g of certified {sup 233}U reference material over the next 50 years. This amount also includes a strategic reserve. To meet this need, 18 individual items totaling 959 g of {sup 233}U were identified as candidates for establishing a lasting supply of certified reference materials (CRM), all having an isotopic purity of at least 99.4% {sup 233}U and including materials up to 99.996% purity. Current plans include rescuing the purest {sup 233}U materials during a 3-year project beginning in FY 2012 in three phases involving preparations, handling preserved materials, and cleanup. The first year will involve preparations for handling the rescued material for sampling, analysis, distribution, and storage. Such preparations involve modifying or developing work control documents and physical preparations in the laboratory, which include preparing space for new material-handling equipment and procuring and (in some cases) refurbishing equipment needed for handling {sup 233}U or qualifying candidate CRM. Once preparations are complete, an evaluation of readiness will be conducted by independent reviewers to verify that the equipment, work controls, and personnel are ready for operations involving handling radioactive materials with nuclear criticality safety as well as radiological control requirements. The material-handling phase will begin in FY 2013 and be completed early in FY 2014, as currently scheduled. Material handling involves retrieving candidate CRM items from the ORNL storage facility and shipping them to another laboratory at ORNL; receiving and handling rescued items at the laboratory (including any needed initial processing, acquisition and analysis of samples from each item, and preparation for shipment); and shipping bulk material to destination labs or to a yet-to-be-designated storage location. There are seven groups of {sup 233}U identified for handling based on isotopic purity that require the utmost care to prevent cross-contamination. The last phase, cleanup, also will be completed in 2014. It involves cleaning and removing the equipment and material-handling boxes and characterizing, documenting, and disposing of waste. As part of initial planning, the cost of rescuing candidate {sup 233}U items was estimated roughly. The annualized costs were found to be $1,228K in FY 2012, $1,375K in FY 2013,

  15. Modeled atmospheric radon concentrations from uranium mines

    SciTech Connect (OSTI)

    Droppo, J.G.

    1985-04-01

    Uranium mining and milling operations result in the release of radon from numerous sources of various types and strengths. The US Environmental Protection Agency (EPA) under the Clean Air Act, is assessing the health impact of air emissions of radon from underground uranium mines. In this case, the radon emissions may impact workers and residents in the mine vicinity. To aid in this assessment, the EPA needs to know how mine releases can affect the radon concentrations at populated locations. To obtain this type of information, Pacific Northwest Laboratory used the radon emissions, release characteristics and local meterological conditions for a number of mines to model incremental radon concentrations. Long-term, average, incremental radon concentrations were computed based on the best available information on release rates, plume rise parameters, number and locations of vents, and local dispersion climatology. Calculations are made for a model mine, individual mines, and multiple mines. Our approach was to start with a general case and then consider specific cases for comparison. A model underground uranium mine was used to provide definition of the order of magnitude of typical impacts. Then computations were made for specific mines using the best mine-specific information available for each mine. These case study results are expressed as predicted incremental radon concentration contours plotted on maps with local population data from a previous study. Finally, the effect of possible overlap of radon releases from nearby mines was studied by calculating cumulative radon concentrations for multiple mines in a region with many mines. The dispersion model, modeling assumptions, data sources, computational procedures, and results are documented in this report. 7 refs., 27 figs., 18 tabs.

  16. Selective Extraction of Uranium from Liquid or Supercritical Carbon Dioxide

    SciTech Connect (OSTI)

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

    2012-07-31

    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.

  17. VANE Uranium One JV | Open Energy Information

    Open Energy Info (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 QA:QA J-E-1 SECTION J APPENDIX ECoop IncIowa (Utility Company) JumpGTZUtility Rates API Version 2(RECP)VANE Uranium One

  18. Manhattan Project: More Uranium Research, 1942

    Office of Scientific and Technical Information (OSTI)

    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 Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfate Reducing(Journalspectroscopy ofArticle)SciTechNorris Bradbury,Cubes of uranium metal, Los

  19. Uranium Weapons Components Successfully Dismantled | 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power AdministrationRobust,Field-effectWorking With WIPPfinalUnexpectedofWyko NT33004. Uranium4.

  20. Nuclear Fuel Facts: Uranium | Department of Energy

    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 DeliciousMathematicsEnergyInterested Parties -DepartmentAvailable forSite |n t e OfficeResearch andFacts: Uranium

  1. Uranium Marketing Annual Report - Energy Information Administration

    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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustments (Billion Cubic Feet) Wyoming Dry NaturalPrices Globaldieselgasolinemonthlysummer gasolineall Uranium

  2. Innovative Elution Processes for Recovering Uranium from Seawater

    SciTech Connect (OSTI)

    Wai, Chien; Tian, Guoxin; Janke, Christopher

    2014-05-29

    Utilizing amidoxime-based polymer sorbents for extraction of uranium from seawater has attracted considerable interest in recent years. Uranium collected in the sorbent is recovered typically by elution with an acid. One drawback of acid elution is deterioration of the sorbent which is a significant factor that limits the economic competitiveness of the amidoxime-based sorbent systems for sequestering uranium from seawater. Developing innovative elution processes to improve efficiency and to minimize loss of sorbent capacity become essential in order to make this technology economically feasible for large-scale industrial applications. This project has evaluated several elution processes including acid elution, carbonate elution, and supercritical fluid elution for recovering uranium from amidoxime-based polymer sorbents. The elution efficiency, durability and sorbent regeneration for repeated uranium adsorption- desorption cycles in simulated seawater have been studied. Spectroscopic techniques are used to evaluate chemical nature of the sorbent before and after elution. A sodium carbonate-hydrogen peroxide elution process for effective removal of uranium from amidoxime-based sorbent is developed. The cause of this sodium carbonate and hydrogen peroxide synergistic leaching of uranium from amidoxime-based sorbent is attributed to the formation of an extremely stable uranyl peroxo-carbonato complex. The efficiency of uranium elution by the carbonate-hydrogen peroxide method is comparable to that of the hydrochloric acid elution but damage to the sorbent material is much less for the former. The carbonate- hydrogen peroxide elution also does not need any elaborate step to regenerate the sorbent as those required for hydrochloric acid leaching. Several CO2-soluble ligands have been tested for extraction of uranium from the sorbent in supercritical fluid carbon dioxide. A mixture of hexafluoroacetylacetone and tri-n-butylphosphate shows the best result but uranium removal from the sorbent reaches only 80% after 10 hours of leaching. Some information regarding coordination of vanadium with amidoxime molecules and elution of vanadium from amidoxime- based sorbents is also given in the report.

  3. Decommissioning of U.S. uranium production facilities

    SciTech Connect (OSTI)

    Not Available

    1995-02-01

    From 1980 to 1993, the domestic production of uranium declined from almost 44 million pounds U{sub 3}O{sub 8} to about 3 million pounds. This retrenchment of the U.S. uranium industry resulted in the permanent closing of many uranium-producing facilities. Current low uranium prices, excess world supply, and low expectations for future uranium demand indicate that it is unlikely existing plants will be reopened. Because of this situation, these facilities eventually will have to be decommissioned. The Uranium Mill Tailings and Radiation Control Act of 1978 (UMTRCA) vests the U.S. Environmental Protection Agency (EPA) with overall responsibility for establishing environmental standards for decommissioning of uranium production facilities. UMTRCA also gave the U.S. Nuclear Regulatory Commission (NRC) the responsibility for licensing and regulating uranium production and related activities, including decommissioning. Because there are many issues associated with decommissioning-environmental, political, and financial-this report will concentrate on the answers to three questions: (1) What is required? (2) How is the process implemented? (3) What are the costs? Regulatory control is exercised principally through the NRC licensing process. Before receiving a license to construct and operate an uranium producing facility, the applicant is required to present a decommissioning plan to the NRC. Once the plan is approved, the licensee must post a surety to guarantee that funds will be available to execute the plan and reclaim the site. This report by the Energy Information Administration (EIA) represents the most comprehensive study on this topic by analyzing data on 33 (out of 43) uranium production facilities located in Colorado, Nebraska, New Mexico, South Dakota, Texas, Utah, and Washington.

  4. Electrorefining process and apparatus for recovery of uranium and a mixture of uranium and plutonium from spent fuels

    DOE Patents [OSTI]

    Ackerman, John P. (Downers Grove, IL); Miller, William E. (Naperville, IL)

    1989-01-01

    An electrorefining process and apparatus for the recovery of uranium and a mixture of uranium and plutonium from spent fuel using an electrolytic cell having a lower molten cadmium pool containing spent nuclear fuel, an intermediate electrolyte pool, an anode basket containing spent fuel, and two cathodes, the first cathode composed of either a solid alloy or molten cadmium and the second cathode composed of molten cadmium. Using this cell, additional amounts of uranium and plutonium from the anode basket are dissolved in the lower molten cadmium pool, and then substantially pure uranium is electrolytically transported and deposited on the first alloy or molten cadmium cathode. Subsequently, a mixture of uranium and plutonium is electrotransported and deposited on the second molten cadmium cathode.

  5. Electrorefining process and apparatus for recovery of uranium and a mixture of uranium and plutonium from spent fuels

    DOE Patents [OSTI]

    Ackerman, J.P.; Miller, W.E.

    1987-11-05

    An electrorefining process and apparatus for the recovery of uranium and a mixture of uranium and plutonium from spent fuels is disclosed using an electrolytic cell having a lower molten cadmium pool containing spent nuclear fuel, an intermediate electrolyte pool, an anode basket containing spent fuels, two cathodes and electrical power means connected to the anode basket, cathodes and lower molten cadmium pool for providing electrical power to the cell. Using this cell, additional amounts of uranium and plutonium from the anode basket are dissolved in the lower molten cadmium pool, and then purified uranium is electrolytically transported and deposited on a first molten cadmium cathode. Subsequently, a mixture of uranium and plutonium is electrotransported and deposited on a second cathode. 3 figs.

  6. Potential remediation approach for uranium-contaminated groundwaters through potassium uranyl vanadate precipitation

    E-Print Network [OSTI]

    Tokunaga, T.K.

    2010-01-01

    Uranium solution-mineral equilibria at low temperatures with applications to sedimentary ore deposits.

  7. DETECTION OF ULTRA-TRACE LEVELS OF URANIUM IN AQUEOUS SAMPLES BY LASER INDUCED FLUORESCENCE SPECTROMETRY

    E-Print Network [OSTI]

    Perry, Dale L.

    2012-01-01

    deposits (especially around nuclear waste repositories) requires rapid, high sensitive analytical techniques. Hydrogeochemical exploration for uranium

  8. Standard practice for the ion exchange separation of uranium and plutonium prior to isotopic analysis

    E-Print Network [OSTI]

    American Society for Testing and Materials. Philadelphia

    2008-01-01

    Standard practice for the ion exchange separation of uranium and plutonium prior to isotopic analysis

  9. Method for removing adhering or dust-like deposits in systems handling uranium hexafluoride

    SciTech Connect (OSTI)

    Bacher, W.; Jacob, E.

    1984-02-28

    A process is claimed for removing adhering or dust-like deposits in an apparatus which handles uranium hexafluoride. The process includes the steps of: (a) reacting the deposits with a gaseous boron halogenide other than boron trifluoride, to form at least one uranium halogenide; and (b) reacting the at least one uranium halogenide with a fluorine containing substance to form uranium hexafluoride.

  10. Stability of uranium incorporated into Fe(hydr)oxides under fluctuating redox conditions

    E-Print Network [OSTI]

    Stewart, B.D.

    2009-01-01

    uranium deposit, Northern Australia - Lessons from the Alligator Rivers analogue project. Physics and Chemistry

  11. Complexation of Gluconate with Uranium(VI) in Acidic Solutions: Thermodynamic Study with Structural Analysis

    E-Print Network [OSTI]

    Zhang, Zhicheng

    2009-01-01

    uranium is approximately one order of magnitude lower than expected, suggesting that the coordination chemistry

  12. MODELING ANISOTROPIC STRESS-STRAIN RESPONSE AND TEXTURE EVOLUTION OF -URANIUM

    E-Print Network [OSTI]

    Mihaila, Bogdan

    MODELING ANISOTROPIC STRESS-STRAIN RESPONSE AND TEXTURE EVOLUTION OF -URANIUM Marko Knezevic Metz, France, laurent.capolungo@me.gatech.edu ABSTRACT The deformation behavior of wrought -uranium, and their role on strain hardening and texture evolution in -uranium. INTRODUCTION: At room temperature -uranium

  13. Occupational exposures to uranium: processes, hazards, and regulations

    SciTech Connect (OSTI)

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

    1981-04-01

    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.

  14. Uranium (VI) solubility in carbonate-free ERDA-6 brine

    SciTech Connect (OSTI)

    Lucchini, Jean-francois; Khaing, Hnin; Reed, Donald T

    2010-01-01

    When present, uranium is usually an element of importance in a nuclear waste repository. In the Waste Isolation Pilot Plant (WIPP), uranium is the most prevalent actinide component by mass, with about 647 metric tons to be placed in the repository. Therefore, the chemistry of uranium, and especially its solubility in the WIPP conditions, needs to be well determined. Long-term experiments were performed to measure the solubility of uranium (VI) in carbonate-free ERDA-6 brine, a simulated WIPP brine, at pC{sub H+} values between 8 and 12.5. These data, obtained from the over-saturation approach, were the first repository-relevant data for the VI actinide oxidation state. The solubility trends observed pointed towards low uranium solubility in WIPP brines and a lack of amphotericity. At the expected pC{sub H+} in the WIPP ({approx} 9.5), measured uranium solubility approached 10{sup -7} M. The objective of these experiments was to establish a baseline solubility to further investigate the effects of carbonate complexation on uranium solubility in WIPP brines.

  15. Method of precipitating uranium from an aqueous solution and/or sediment

    DOE Patents [OSTI]

    Tokunaga, Tetsu K; Kim, Yongman; Wan, Jiamin

    2013-08-20

    A method for precipitating uranium from an aqueous solution and/or sediment comprising uranium and/or vanadium is presented. The method includes precipitating uranium as a uranyl vanadate through mixing an aqueous solution and/or sediment comprising uranium and/or vanadium and a solution comprising a monovalent or divalent cation to form the corresponding cation uranyl vanadate precipitate. The method also provides a pathway for extraction of uranium and vanadium from an aqueous solution and/or sediment.

  16. Heavy Ion Beam in Resolution of the Critical Point Problem for Uranium and Uranium Dioxide

    E-Print Network [OSTI]

    Iosilevskiy, Igor

    2010-01-01

    Important advantages of heavy ion beam (HIB) irradiation of matter are discussed in comparison with traditional sources - laser heating, electron beam, electrical discharge etc. High penetration length (~ 10 mm) is of primary importance for investigation of dense matter properties. This gives an extraordinary chance to reach the uniform heating regime when HIB irradiation is being used for thermophysical property measurements. Advantages of HIB heating of highly-dispersive samples are claimed for providing free and relatively slow quasi-isobaric heating without fast hydrodynamic expansion of heated sample. Perspective of such HIB application are revised for resolution of long-time thermophysical problems for uranium and uranium-bearing compounds (UO2). The priorities in such HIB development are stressed: preferable energy levels, beam-time duration, beam focusing, deposition of the sample etc.

  17. Heavy Ion Beam in Resolution of the Critical Point Problem for Uranium and Uranium Dioxide

    E-Print Network [OSTI]

    Igor Iosilevskiy; Victor Gryaznov

    2010-05-23

    Important advantages of heavy ion beam (HIB) irradiation of matter are discussed in comparison with traditional sources - laser heating, electron beam, electrical discharge etc. High penetration length (~ 10 mm) is of primary importance for investigation of dense matter properties. This gives an extraordinary chance to reach the uniform heating regime when HIB irradiation is being used for thermophysical property measurements. Advantages of HIB heating of highly-dispersive samples are claimed for providing free and relatively slow quasi-isobaric heating without fast hydrodynamic expansion of heated sample. Perspective of such HIB application are revised for resolution of long-time thermophysical problems for uranium and uranium-bearing compounds (UO2). The priorities in such HIB development are stressed: preferable energy levels, beam-time duration, beam focusing, deposition of the sample etc.

  18. Modeling non-steady state radioisotope transport in the vadose zone--A case study using uranium isotopes at Pena Blanca, Mexico

    E-Print Network [OSTI]

    Ku, T. L.

    2010-01-01

    map of the Nopal I uranium deposit, indicating the locationflow at the Nopal I uranium deposit, Sierra Peña Blanca,Chihuahua, Mexico. In: Uranium Deposits in Volcanic Rocks,

  19. Uranium and other heavy metals in the plant-animal-human food chain near abandoned mining sites and structures in an American Indian community in northwestern New Mexico

    E-Print Network [OSTI]

    Samuel-Nakamura, Christine

    2013-01-01

    environment of uranium deposits of the Grants region, Newan area with large uranium deposits. The area was initiallyepigenetic sandstone uranium ore deposits, the predominant

  20. Uranium and other heavy metals in the plant-animal-human food chain near abandoned mining sites and structures in an American Indian community in northwestern New Mexico

    E-Print Network [OSTI]

    Samuel-Nakamura, Christine

    2013-01-01

    of risk maps to minimize uranium exposures in the NavajoThe Navajo people and uranium mining. Albuquerque, NM:toxicity of natural uranium: A review. Reviews on

  1. Uranium 238U/235U isotope ratios as indicators of reduction: Results from an in situ biostimulation experiment at Rifle, Colorado, USA

    E-Print Network [OSTI]

    Bopp IV, C.J.

    2010-01-01

    Series Geochemistry; In Uranium-Series Geochemistry; BernardIsotopic Fractionation of Uranium. Earth and Planetaryand precipitation of uranium and vanadium at low

  2. High temperature behavior of metallic inclusions in uranium dioxide

    SciTech Connect (OSTI)

    Yang, R.L.

    1980-08-01

    The object of this thesis was to construct a temperature gradient furnace to simulate the thermal conditions in the reactor fuel and to study the migration of metallic inclusions in uranium oxide under the influence of temperature gradient. No thermal migration of molybdenum and tungsten inclusions was observed under the experimental conditions. Ruthenium inclusions, however, dissolved and diffused atomically through grain boundaries in slightly reduced uranium oxide. An intermetallic compound (probably URu/sub 3/) was formed by reaction of Ru and UO/sub 2-x/. The diffusivity and solubility of ruthenium in uranium oxide were measured.

  3. Characterization of Thermal Properties of Depleted Uranium Metal Microspheres 

    E-Print Network [OSTI]

    Humrickhouse, Carissa Joy

    2012-07-16

    llment of the requirements for the degree of MASTER OF SCIENCE Approved by: Chair of Committee, Sean M. McDeavitt Committee Members, Kenneth L. Peddicord Lin Shao Head of Department, Yassin A. Hassan May 2012 Major Subject: Nuclear Engineering iii.../m-K) Density (units: g/cm3) CHTA Crucible Heater Test Assembly DU Depleted uranium EU Enriched uranium LFA Laser (or light) ash analysis LFA 447 Light ash analyzer, model 447, by Netzsch Instruments LWR Light water reactor ODU Oxidized depleted uranium...

  4. Uranium Track Team | 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: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power AdministrationRobust,Field-effectWorking With WIPPfinalUnexpectedofWyko NT33004. Uranium4. UraniumUraniumTrack

  5. TRIMOLECULAR REACTIONS OF URANIUM HEXAFLUORIDE WITH WATER

    SciTech Connect (OSTI)

    Westbrook, M.; Becnel, J.; Garrison, S.

    2010-02-25

    The hydrolysis reaction of uranium hexafluoride (UF{sub 6}) is a key step in the synthesis of uranium dioxide (UO{sub 2}) powder for nuclear fuels. Mechanisms for the hydrolysis reactions are studied here with density functional theory and the Stuttgart small-core scalar relativistic pseudopotential and associated basis set for uranium. The reaction of a single UF{sub 6} molecule with a water molecule in the gas phase has been previously predicted to proceed over a relatively sizeable barrier of 78.2 kJ {center_dot} mol{sup -1}, indicating this reaction is only feasible at elevated temperatures. Given the observed formation of a second morphology for the UO{sub 2} product coupled with the observations of rapid, spontaneous hydrolysis at ambient conditions, an alternate reaction pathway must exist. In the present work, two trimolecular hydrolysis mechanisms are studied with density functional theory: (1) the reaction between two UF{sub 6} molecules and one water molecule, and (2) the reaction of two water molecules with a single UF{sub 6} molecule. The predicted reaction of two UF{sub 6} molecules with one water molecule displays an interesting 'fluorine-shuttle' mechanism, a significant energy barrier of 69.0 kJ {center_dot} mol{sup -1} to the formation of UF{sub 5}OH, and an enthalpy of reaction ({Delta}H{sub 298}) of +17.9 kJ {center_dot} mol{sup -1}. The reaction of a single UF{sub 6} molecule with two water molecules displays a 'proton-shuttle' mechanism, and is more favorable, having a slightly lower computed energy barrier of 58.9 kJ {center_dot} mol{sup -1} and an exothermic enthalpy of reaction ({Delta}H{sub 298}) of -13.9 kJ {center_dot} mol{sup -1}. The exothermic nature of the overall UF{sub 6} + 2 {center_dot} H{sub 2}O trimolecular reaction and the lowering of the barrier height with respect to the bimolecular reaction are encouraging; however, the sizable energy barrier indicates further study of the UF{sub 6} hydrolysis reaction mechanism is warranted to resolve the remaining discrepancies between the predicted mechanisms and experimental observations.

  6. Uranium-series constraints on radionuclide transport and groundwater flow at the Nopal I uranium deposit, Sierra Pena Blanca, Mexico

    SciTech Connect (OSTI)

    Goldstein, S.J.; Abdel-Fattah, A.I.; Murrell, M.T.; Dobson, P.F.; Norman, D.E.; Amato, R.S.; Nunn, A. J.

    2009-10-01

    Uranium-series data for groundwater samples from the Nopal I uranium ore deposit were obtained to place constraints on radionuclide transport and hydrologic processes for a nuclear waste repository located in fractured, unsaturated volcanic tuff. Decreasing uranium concentrations for wells drilled in 2003 are consistent with a simple physical mixing model that indicates that groundwater velocities are low ({approx}10 m/y). Uranium isotopic constraints, well productivities, and radon systematics also suggest limited groundwater mixing and slow flow in the saturated zone. Uranium isotopic systematics for seepage water collected in the mine adit show a spatial dependence which is consistent with longer water-rock interaction times and higher uranium dissolution inputs at the front adit where the deposit is located. Uranium-series disequilibria measurements for mostly unsaturated zone samples indicate that {sup 230}Th/{sup 238}U activity ratios range from 0.005-0.48 and {sup 226}Ra/{sup 238}U activity ratios range from 0.006-113. {sup 239}Pu/{sup 238}U mass ratios for the saturated zone are <2 x 10{sup -14}, and Pu mobility in the saturated zone is >1000 times lower than the U mobility. Saturated zone mobility decreases in the order {sup 238}U{approx}{sup 226}Ra > {sup 230}Th{approx}{sup 239}Pu. Radium and thorium appear to have higher mobility in the unsaturated zone based on U-series data from fractures and seepage water near the deposit.

  7. Analysis of uranium urinalysis and in vivo measurement results from eleven participating uranium mills

    SciTech Connect (OSTI)

    Spitz, H.B.; Simpson, J.C.; Aldridge, T.L.

    1984-05-01

    Uranium urinalysis and in vivo examination results obtained from workers at eleven uranium mills between 1978 and 1980 were evaluated. The main purpose was to determine the degree of the mills' compliance with bioassay monitoring recommendations given in the draft NRC Regulatory Guide 8.22 (USNRC 1978). The effect of anticipated changes in the draft regulatory guidance, as expressed to PNL in May 1982, was also studied. Statistical analyses of the data showed that the bioassay results did not reliably meet the limited performance criteria given in the draft regulatory guide. Furthermore, quality control measurements of uranium in urine indicated that detection limits at ..cap alpha.. = ..beta.. = 0.05 ranged from 13 ..mu..g/l to 29 ..mu..g/l, whereas the draft regulatory guidance suggests 5 ..mu..g/l as the detection limit. Recommendations for monitoring frequencies given in the draft guide were not followed consistently from mill to mill. The results of these statistical analyses indicate a need to include performance criteria for accuracy, precision, and confidence in revisions of the draft Regulatory Guide 8.22. Revised guidance should also emphasize the need for each mill to continually test the laboratory performing urinalyses by submitting quality control samples (i.e., blank and spiked urine samples as open and blind test) to insure that the performance criteria are being met. Recommendations for a bioassay audit program are also given. 25 references, 15 figures, 17 tables.

  8. Small cell experiments for electrolytic reduction of uranium oxides to uranium metal using fluoride salts

    SciTech Connect (OSTI)

    Haas, P.A.; Adcock, P.W.; Coroneos, A.C.; Hendrix, D.E. )

    1994-08-01

    Electrolytic reduction of uranium oxide was proposed for the preparation of uranium metal feed for the atomic vapor laser isotope separation (AVLIS) process. A laboratory cell of 25-cm ID was operated to obtain additional information in areas important to design and operation of a pilot plant cell. Reproducible test results and useful operating and control procedures were demonstrated. About 20 kg of uranium metal of acceptable purity were prepared. A good supply of dissolved UO[sub 2] feed at the anode is the most important controlling requirement for efficient cell operation. A large fraction of the cell current is nonproductive in that it does not produce a metal product nor consume carbon anodes. All useful test conditions gave some reduction of UF[sub 4] to produce CF[sub 4] in addition to the reduction of UO[sub 2], but the fraction of metal from the reduction of UF[sub 4] can be decreased by increasing the concentration of dissolved UO[sub 2]. Operation of large continuous cells would probably be limited to current efficiencies of less than 60 pct, and more than 20 pct of the metal would result from the reduction of UF[sub 4].

  9. Novel Sensor for the In Situ Measurement of Uranium Fluxes

    SciTech Connect (OSTI)

    Hatfield, Kirk

    2015-02-10

    The goal of this project was to develop a sensor that incorporates the field-tested concepts of the passive flux meter to provide direct in situ measures of flux for uranium and groundwater in porous media. Measurable contaminant fluxes [J] are essentially the product of concentration [C] and groundwater flux or specific discharge [q ]. The sensor measures [J] and [q] by changes in contaminant and tracer amounts respectively on a sorbent. By using measurement rather than inference from static parameters, the sensor can directly advance conceptual and computational models for field scale simulations. The sensor was deployed in conjunction with DOE in obtaining field-scale quantification of subsurface processes affecting uranium transport (e.g., advection) and transformation (e.g., uranium attenuation) at the Rifle IFRC Site in Rifle, Colorado. Project results have expanded our current understanding of how field-scale spatial variations in fluxes of uranium, groundwater and salient electron donor/acceptors are coupled to spatial variations in measured microbial biomass/community composition, effective field-scale uranium mass balances, attenuation, and stability. The coupling between uranium, various nutrients and micro flora can be used to estimate field-scale rates of uranium attenuation and field-scale transitions in microbial communities. This research focuses on uranium (VI), but the sensor principles and design are applicable to field-scale fate and transport of other radionuclides. Laboratory studies focused on sorbent selection and calibration, along with sensor development and validation under controlled conditions. Field studies were conducted at the Rifle IFRC Site in Rifle, Colorado. These studies were closely coordinated with existing SBR (formerly ERSP) projects to complement data collection. Small field tests were conducted during the first two years that focused on evaluating field-scale deployment procedures and validating sensor performance under controlled field conditions. In the third and fourth year a suite of larger field studies were conducted. For these studies, the uranium flux sensor was used with uranium speciation measurements and molecular-biological tools to characterize microbial community and active biomass at synonymous wells distributed in a large grid. These field efforts quantified spatial changes in uranium flux and field-scale rates of uranium attenuation (ambient and stimulated), uranium stability, and quantitatively assessed how fluxes and effective reaction rates were coupled to spatial variations in microbial community and active biomass. Analyses of data from these field experiments were used to generate estimates of Monod kinetic parameters that are ‘effective’ in nature and optimal for modeling uranium fate and transport at the field-scale. This project provided the opportunity to develop the first sensor that provides direct measures of both uranium (VI) and groundwater flux. A multidisciplinary team was assembled to include two geochemists, a microbiologist, and two quantitative contaminant hydrologists. Now that the project is complete, the sensor can be deployed at DOE sites to evaluate field-scale uranium attenuation, source behavior, the efficacy of remediation, and off-site risk. Because the sensor requires no power, it can be deployed at remote sites for periods of days to months. The fundamental science derived from this project can be used to advance the development of predictive models for various transport and attenuation processes in aquifers. Proper development of these models is critical for long-term stewardship of contaminated sites in the context of predicting uranium source behavior, remediation performance, and off-site risk.

  10. Developing fuel management capabilities based on coupled Monte Carlo depletion in support of the MIT Research Reactor (MITR) conversion

    E-Print Network [OSTI]

    Romano, Paul K. (Paul Kollath)

    2009-01-01

    Pursuant to a 1986 NRC ruling, the MIT Reactor (MITR) is planning on converting from the use of highly enriched uranium (HEU) to low enriched uranium (LEU) for fuel. Prior studies have shown that the MITR will be able to ...

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

    E-Print Network [OSTI]

    Connaway, Heather M. (Heather Moira)

    2012-01-01

    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 of a global effort to minimize the availability of ...

  12. Deputy Secretary Daniel Poneman's Remarks to the International...

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

    uranium from the Kazakh Institute of Nuclear Physics in Almaty. The resulting low-enriched uranium cannot be redirected for use in nuclear weapons. Instead, it will be returned...

  13. Two U.S. University Research Reactors to be Converted From Highly...

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

    of Energy (DOE) has begun to convert research reactors from using highly-enriched uranium (HEU) to low-enriched uranium fuel (LEU) at the University of Florida and Texas A&M...

  14. US developments in technology for uranium enrichment

    SciTech Connect (OSTI)

    Wilcox, W.J. Jr.; McGill, R.M.

    1982-01-01

    The purpose of this paper is to review recent progress and the status of the work in the United States on that part of the fuel cycle concerned with uranium enrichment. The United States has one enrichment process, gaseous diffusion, which has been continuously operated in large-scale production for the past 37 years; another process, gas centrifugation, which is now in the construction phase; and three new processes, molecular laser isotope separation, atomic vapor laser isotope separation, plasma separation process, in which the US has also invested sizable research and development efforts over the last few years. The emphasis in this paper is on the technical aspects of the various processes, but the important economic factors which will define the technological mix which may be applied in the next two decades are also discussed.

  15. Molten uranium dioxide structure and dynamics

    SciTech Connect (OSTI)

    Skinner, L. B. [Argonne National Laboratory (ANL), Argonne, IL (United States); Stony Brook Univ., Stony Brook, NY (United States); Materials Development Inc., Arlington Heights, IL (United States); Parise, J. B. [Stony Brook Univ., Stony Brook, NY (United States); Benmore, C. J. [Argonne National Laboratory (ANL), Argonne, IL (United States); Weber, J. K.R. [Materials Development Inc., Arlington Heights, IL (United States); Williamson, M. A. [Argonne National Laboratory (ANL), Argonne, IL (United States); Tamalonis, A. [Materials Development Inc., Arlington Heights, IL (United States); Hebden, A. [Argonne National Laboratory (ANL), Argonne, IL (United States); Wiencek, T. [Argonne National Laboratory (ANL), Argonne, IL (United States); Alderman, O. L.G. [Materials Development Inc., Arlington Heights, IL (United States); Guthrie, M. [Carnegie Inst., Washington, DC (United States); Leibowitz, L. [Argonne National Laboratory (ANL), Argonne, IL (United States)

    2014-11-20

    Uranium dioxide (UO2) is the major nuclear fuel component of fission power reactors. A key concern during severe accidents is the melting and leakage of radioactive UO2 as it corrodes through its zirconium cladding and steel containment. Yet, the very high temperatures (>3140 kelvin) and chemical reactivity of molten UO2 have prevented structural studies. In this work, we combine laser heating, sample levitation, and synchrotron x-rays to obtain pair distribution function measurements of hot solid and molten UO2. The hot solid shows a substantial increase in oxygen disorder around the lambda transition (2670 K) but negligible U-O coordination change. On melting, the average U-O coordination drops from 8 to 6.7 ± 0.5. Molecular dynamics models refined to this structure predict higher U-U mobility than 8-coordinated melts.

  16. Molten uranium dioxide structure and dynamics

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Skinner, L. B. [Argonne National Laboratory (ANL), Argonne, IL (United States); Stony Brook Univ., Stony Brook, NY (United States); Materials Development Inc., Arlington Heights, IL (United States); Parise, J. B. [Stony Brook Univ., Stony Brook, NY (United States); Benmore, C. J. [Argonne National Laboratory (ANL), Argonne, IL (United States); Weber, J. K.R. [Materials Development Inc., Arlington Heights, IL (United States); Williamson, M. A. [Argonne National Laboratory (ANL), Argonne, IL (United States); Tamalonis, A. [Materials Development Inc., Arlington Heights, IL (United States); Hebden, A. [Argonne National Laboratory (ANL), Argonne, IL (United States); Wiencek, T. [Argonne National Laboratory (ANL), Argonne, IL (United States); Alderman, O. L.G. [Materials Development Inc., Arlington Heights, IL (United States); Guthrie, M. [Carnegie Inst., Washington, DC (United States); Leibowitz, L. [Argonne National Laboratory (ANL), Argonne, IL (United States)

    2014-11-20

    Uranium dioxide (UO2) is the major nuclear fuel component of fission power reactors. A key concern during severe accidents is the melting and leakage of radioactive UO2 as it corrodes through its zirconium cladding and steel containment. Yet, the very high temperatures (>3140 kelvin) and chemical reactivity of molten UO2 have prevented structural studies. In this work, we combine laser heating, sample levitation, and synchrotron x-rays to obtain pair distribution function measurements of hot solid and molten UO2. The hot solid shows a substantial increase in oxygen disorder around the lambda transition (2670 K) but negligible U-O coordination change. On melting, the average U-O coordination drops from 8 to 6.7 ± 0.5. Molecular dynamics models refined to this structure predict higher U-U mobility than 8-coordinated melts.

  17. Molten uranium dioxide structure and dynamics

    SciTech Connect (OSTI)

    Skinner, L. B.; Parise, J. B.; Benmore, C. J.; Weber, J. K.R.; Williamson, M. A.; Tamalonis, A.; Hebden, A.; Wiencek, T.; Alderman, O. L.G.; Guthrie, M.; Leibowitz, L.

    2014-11-21

    Uranium dioxide (UO2) is the major nuclear fuel component of fission power reactors. A key concern during severe accidents is the melting and leakage of radioactive UO2 as it corrodes through its zirconium cladding and steel containment. Yet, the very high temperatures (>3140 kelvin) and chemical reactivity of molten UO2 have prevented structural studies. In this work, we combine laser heating, sample levitation, and synchrotron x-rays to obtain pair distribution function measurements of hot solid and molten UO2. The hot solid shows a substantial increase in oxygen disorder around the lambda transition (2670 K) but negligible U-O coordination change. On melting, the average U-O coordination drops from 8 to 6.7 ± 0.5. Molecular dynamics models refined to this structure predict higher U-U mobility than 8-coordinated melts.

  18. Molten uranium dioxide structure and dynamics

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Skinner, L. B.; Parise, J. B.; Benmore, C. J.; Weber, J. K.R.; Williamson, M. A.; Tamalonis, A.; Hebden, A.; Wiencek, T.; Alderman, O. L.G.; Guthrie, M.; et al

    2014-11-21

    Uranium dioxide (UO2) is the major nuclear fuel component of fission power reactors. A key concern during severe accidents is the melting and leakage of radioactive UO2 as it corrodes through its zirconium cladding and steel containment. Yet, the very high temperatures (>3140 kelvin) and chemical reactivity of molten UO2 have prevented structural studies. In this work, we combine laser heating, sample levitation, and synchrotron x-rays to obtain pair distribution function measurements of hot solid and molten UO2. The hot solid shows a substantial increase in oxygen disorder around the lambda transition (2670 K) but negligible U-O coordination change. Onmore »melting, the average U-O coordination drops from 8 to 6.7 ± 0.5. Molecular dynamics models refined to this structure predict higher U-U mobility than 8-coordinated melts.« less

  19. Systems studies on the extraction of uranium from seawater

    E-Print Network [OSTI]

    Driscoll, Michael J.

    1981-01-01

    This report summarizes the work done at MIT during FY 1981 on the overall system design of a uranium-from-seawater facility. It consists of a sequence of seven major chapters, each of which was originally prepared as a ...

  20. Uncertainty analysis of multi-rate kinetics of uranium desorption...

    Office of Scientific and Technical Information (OSTI)

    multi-rate kinetics of uranium desorption from sediments A multi-rate expression for uranyl U(VI) surface complexation reactions has been proposed to describe diffusion-limited...

  1. Method to remove uranium/vanadium contamination from groundwater

    DOE Patents [OSTI]

    Metzler, Donald R. (DeBeque, CO); Morrison, Stanley (Grand Junction, CO)

    2004-07-27

    A process for removing uranium/vanadium-based contaminants from groundwater using a primary in-ground treatment media and a pretreatment media that chemically adjusts the groundwater contaminant to provide for optimum treatment by the primary treatment media.

  2. Radiation and Uranium Resources Exposure Control (South Dakota)

    Broader source: Energy.gov [DOE]

    The public policy of South Dakota is to encourage the constructive uses of radiation, the proper development of uranium resources, and the control of any associated harmful effects. The disposal of...

  3. Fuel cycle optimization of thorium and uranium fueled PWR systems

    E-Print Network [OSTI]

    Garel, Keith Courtnay

    1977-01-01

    The burnup neutronics of uniform PWR lattices are examined with respect to reduction of uranium ore requirements with an emphasis on variation of the fuel-to-moderator ratio

  4. Final report on improved uranium utilization in PWRs

    E-Print Network [OSTI]

    Driscoll, Michael J.

    1982-01-01

    This is the final summary progress report on a research program carried out within the MIT Energy Laboratory/Nuclear Engineering Department under the US Department of Energy's program to increase the effectiveness of uranium ...

  5. DOE Evaluates Environmental Impacts of Uranium Mining on Government...

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

    25,000 acres - that are leased to private entities for uranium and vanadium mining. There have been three previous leasing periods on the tracts since the program was...

  6. Safeguards for Uranium Extraction (UREX) +1a Process 

    E-Print Network [OSTI]

    Feener, Jessica S.

    2011-08-08

    As nuclear energy grows in the United States and around the world, the expansion of the nuclear fuel cycle is inevitable. All currently deployed commercial reprocessing plants are based on the Plutonium - Uranium Extraction ...

  7. Toxic Substances Control Act Uranium Enrichment Federal Facilities...

    Office of Environmental Management (EM)

    Thomas L. McCall, Jr. http:www.em.doe.govffaaortsca.html 4252001 Toxic Substances Control Act Uranium Enrichment Federal Facilities Compliance Agree.. Page 12 of 26 Deputy...

  8. U.S. Uranium Reserves Estimates - Energy Information Administration

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

    all Nuclear Reports U.S. Uranium Reserves Estimates Data for: 2008 | Release Date: July 2010 | Next Release Date: Discontinued The U.S. Energy Information Administration (EIA) has...

  9. Legacy Management Work Progresses on Defense-Related Uranium...

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

    (LM) continues to work on a report to Congress regarding defense-related legacy uranium mines. LM was directed by the U.S. Congress in the National Defense Authorization Act...

  10. Speciation of Uranium in Biologically Reduced Sediments in the...

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

    Speciation of Uranium in Biologically Reduced Sediments in the Old Rifle Aquifer Wednesday, May 16, 2012 - 1:30pm SSRL Conference Room 137-322 Juan S. Lezama Pacheco The speciation...

  11. Solidification/stabilization of simulated uranium and nickel contaminated sludges 

    E-Print Network [OSTI]

    Ramabhadran, Sanjay

    1996-01-01

    Research missions in nuclear energy conducted by the U.S. Department of Energy facilities have generated large volumes of mixed wastes with hazardous and radioactive components. Uranium and nickel are the primary contaminants of concern...

  12. Uranium Adsorption on Granular Activated Carbon – Batch Testing

    SciTech Connect (OSTI)

    Parker, Kent E.; Golovich, Elizabeth C.; Wellman, Dawn M.

    2013-09-26

    The uranium adsorption performance of two activated carbon samples (Tusaar Lot B-64, Tusaar ER2-189A) was tested using unadjusted source water from well 299-W19-36. These batch tests support ongoing performance optimization efforts to use the best material for uranium treatment in the Hanford Site 200 West Area groundwater pump-and-treat system. A linear response of uranium loading as a function of the solution-to-solid ratio was observed for both materials. Kd values ranged from ~380,000 to >1,900,000 ml/g for the B-64 material and ~200,000 to >1,900,000 ml/g for the ER2-189A material. Uranium loading values ranged from 10.4 to 41.6 ?g/g for the two Tusaar materials.

  13. Method to Remove Uranium/Vanadium Contamination from Groundwater

    DOE Patents [OSTI]

    Metzler, Donald R.; Morrison Stanley

    2004-07-27

    A process for removing uranium/vanadium-based contaminants from groundwater using a primary in-ground treatment media and a pretreatment media that chemically adjusts the groundwater contaminant to provide for optimum treatment by the primary treatment media.

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

    SciTech Connect (OSTI)

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

    2008-12-23

    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

  15. Uranium - thorium series study on Yucatan slope cores 

    E-Print Network [OSTI]

    Exner, Mary Elizabeth

    1972-01-01

    URANIUM ? THORIUM SERIES STUDY ON YUCATAN SLOPE CORES A Thesis by Mary Elizabeth Exner Submitted to the Graduate College of Texas A&M University in partial fulfillment of the requirement for the degree of MASTER OF SCIENCE August, 1972... Major Subject: Oceanography URANIUM ? THORIUM SERIES STUDY ON YUCATAN SLOPE CORES A Thesis by Mary Elizabeth Exner Approved as to style and content by: (Chairman of ommittee) , 1 (Head of Department)' p (Member ) (Member) August, 1972 gg...

  16. Pentavalent Uranium Chemistry - Synthetic Pursuit Of A Rare Oxidation State

    SciTech Connect (OSTI)

    Graves, Christopher R; Kiplinger, Jaqueline L

    2009-01-01

    This feature article presents a comprehensive overview of pentavalent uranium systems in non-aqueous solution with a focus on the various synthetic avenues employed to access this unusual and very important oxidation state. Selected characterization data and theoretical aspects are also included. The purpose is to provide a perspective on this rapidly evolving field and identify new possibilities for future developments in pentavalent uranium chemistry.

  17. Geological and geochemical aspects of uranium deposits. A selected, annotated bibliography

    SciTech Connect (OSTI)

    Garland, P.A.; Thomas, J.M.; Brock, M.L.; Daniel, E.W.

    1980-06-01

    A bibliography of 479 references encompassing the fields of uranium and thorium geochemistry and mineralogy, geology of uranium deposits, uranium mining, and uranium exploration techniques has been compiled by the Ecological Sciences Information Center of Oak Ridge National Laboratory. The bibliography was produced for the National Uranium Resource Evaluation Program, which is funded by the Grand Junction Office of the Department of Energy. The references contained in the bibliography have been divided into the following eight subject categories: (1) geology of deposits, (2) geochemistry, (3) genesis O deposits, (4) exploration, (5) mineralogy, (6) uranium industry, (7) reserves and resources, and (8) geology of potential uranium-bearing areas. All categories specifically refer to uranium and thorium; the last category contains basic geologic information concerning areas which the Grand Junction Office feels are particularly favorable for uranium deposition. The references are indexed by author, geographic location, quadrangle name, geoformational feature, taxonomic name, and keyword.

  18. Uranium Biomineralization by Natural Microbial Phosphatase Activities in the Subsurface

    SciTech Connect (OSTI)

    Sobecky, Patricia A.

    2015-04-06

    In this project, inter-disciplinary research activities were conducted in collaboration among investigators at The University of Alabama (UA), Georgia Institute of Technology (GT), Lawrence Berkeley National Laboratory (LBNL), Brookhaven National Laboratory (BNL), the DOE Joint Genome Institute (JGI), and the Stanford Synchrotron Radiation Light source (SSRL) to: (i) confirm that phosphatase activities of subsurface bacteria in Area 2 and 3 from the Oak Ridge Field Research Center result in solid U-phosphate precipitation in aerobic and anaerobic conditions; (ii) investigate the eventual competition between uranium biomineralization via U-phosphate precipitation and uranium bioreduction; (iii) determine subsurface microbial community structure changes of Area 2 soils following organophosphate amendments; (iv) obtain the complete genome sequences of the Rahnella sp. Y9-602 and the type-strain Rahnella aquatilis ATCC 33071 isolated from these soils; (v) determine if polyphosphate accumulation and phytate hydrolysis can be used to promote U(VI) biomineralization in subsurface sediments; (vi) characterize the effect of uranium on phytate hydrolysis by a new microorganism isolated from uranium-contaminated sediments; (vii) utilize positron-emission tomography to label and track metabolically-active bacteria in soil columns, and (viii) study the stability of the uranium phosphate mineral product. Microarray analyses and mineral precipitation characterizations were conducted in collaboration with DOE SBR-funded investigators at LBNL. Thus, microbial phosphorus metabolism has been shown to have a contributing role to uranium immobilization in the subsurface.

  19. The IMCA: A field instrument for uranium enrichment measurements

    SciTech Connect (OSTI)

    Gardner, G.H.; Koskelo, M.; Moeslinger, M.; Mayer, R.L. II; McGinnis, B.R.; Wishard, B.

    1996-12-31

    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.

  20. Standard specification for sintered gadolinium oxide-uranium dioxide pellets

    E-Print Network [OSTI]

    American Society for Testing and Materials. Philadelphia

    2008-01-01

    1.1 This specification is for finished sintered gadolinium oxide-uranium dioxide pellets for use in light-water reactors. It applies to gadolinium oxide-uranium dioxide pellets containing uranium of any 235U concentration and any concentration of gadolinium oxide. 1.2 This specification recognizes the presence of reprocessed uranium in the fuel cycle and consequently defines isotopic limits for gadolinium oxide-uranium dioxide pellets made from commercial grade UO2. Such commercial grade UO2 is defined so that, regarding fuel design and manufacture, the product is essentially equivalent to that made from unirradiated uranium. UO2 falling outside these limits cannot necessarily be regarded as equivalent and may thus need special provisions at the fuel fabrication plant or in the fuel design. 1.3 This specification does not include (1) provisions for preventing criticality accidents or (2) requirements for health and safety. Observance of this specification does not relieve the user of the obligation to be aw...

  1. Sampling Plan for Assaying Plates Containing Depleted or Normal Uranium

    SciTech Connect (OSTI)

    Ivan R. Thomas

    2011-11-01

    This paper describes the rationale behind the proposed method for selecting a 'representative' sample of uranium metal plates, portions of which will be destructively assayed at the Y-12 Security Complex. The total inventory of plates is segregated into two populations, one for Material Type 10 (depleted uranium (DU)) and one for Material Type 81 (normal [or natural] uranium (NU)). The plates within each population are further stratified by common dimensions. A spreadsheet gives the collective mass of uranium element (and isotope for DU) and the piece count of all plates within each stratum. These data are summarized in Table 1. All plates are 100% uranium metal, and all but approximately 60% of the NU plates have Kel-F{reg_sign} coating. The book inventory gives an overall U-235 isotopic percentage of 0.22% for the DU plates, ranging from 0.19% to 0.22%. The U-235 ratio of the NU plates is assumed to be 0.71%. As shown in Table 1, the vast majority of the plates are comprised of depleted uranium, so most of the plates will be sampled from the DU population.

  2. Diffusion model of the non-stoichiometric uranium dioxide

    SciTech Connect (OSTI)

    Moore, Emily, E-mail: emily.moore@cea.fr [CEA Saclay, DEN-DPC-SCCME, 91191 Gif-sur-Yvette Cedex (France); Guéneau, Christine, E-mail: christine.gueneau@cea.fr [CEA Saclay, DEN-DPC-SCCME, 91191 Gif-sur-Yvette Cedex (France); Crocombette, Jean-Paul, E-mail: jean-paul.crocombette@cea.fr [CEA Saclay, DEN DEN, Service de Recherches de Métallurgie Physique, 91191 Gif-sur-Yvette Cedex (France)

    2013-07-15

    Uranium dioxide (UO{sub 2}), which is used in light water reactors, exhibits a large range of non-stoichiometry over a wide temperature scale up to 2000 K. Understanding diffusion behavior of uranium oxides under such conditions is essential to ensure safe reactor operation. The current understanding of diffusion properties is largely limited by the stoichiometric deviations inherent to the fuel. The present DICTRA-based model considers diffusion across non-stoichiometric ranges described by experimentally available data. A vacancy and interstitial model of diffusion is applied to the U–O system as a function of its defect structure derived from CALPHAD-type thermodynamic descriptions. Oxygen and uranium self and tracer diffusion coefficients are assessed for the construction of a mobility database. Chemical diffusion coefficients of oxygen are derived with respect to the Darken relation and migration energies of defects are evaluated as a function of stoichiometric deviation. - Graphical abstract: Complete description of Oxygen–Uranium diffusion as a function of composition at various temperatures according to the developed Dictra model. - Highlights: • Assessment of a uranium–oxygen diffusion model with Dictra. • Complete description of U–O diffusion over wide temperature and composition range. • Oxygen model includes terms for interstitial and vacancy migration. • Interaction terms between defects help describe non-stoichiometric domain of UO{sub 2±x}. • Uranium model is separated into mobility terms for the cationic species.

  3. Engineering analysis report for the long-term management of depleted uranium hexafluoride : storage of depleted uranium metal.

    SciTech Connect (OSTI)

    Folga, S.M.; Kier, P.H.; Thimmapuram, P.R.

    2001-01-24

    This report contains an engineering analysis of long-term storage of uranium metal in boxes as an option for long-term management of depleted uranium hexafluoride (UF{sub 6}). Three storage facilities are considered: buildings, vaults, and mined cavities. Three cases are considered: either all, half, or a quarter of the depleted uranium metal that would be produced from the conversion of depleted UF{sub 6} is stored at the facility. The analysis of these alternatives is based on a box design used in the Final Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted Uranium Hexafluoride, report DOE/EIS-0269, published in 1999 by the US Department of Energy. This box design does not appear to effectively use space within the box. Hence, an alternative box design that allows for a reduced storage area is addressed in the appendices for long-term storage in buildings.

  4. EIS-0126: Remedial Actions at the Former Climax Uranium Company Uranium Mill Site, Grand Junction, Mesa County, Colorado

    Broader source: Energy.gov [DOE]

    The U.S. Department of Energy developed this EIS to assess the environmental impacts of remediating the residual radioactive materials left from the inactive uranium processing site and associated properties located in Grand Junction, Colorado.

  5. Standard test method for the determination of uranium by ignition and the oxygen to uranium (O/U) atomic ratio of nuclear grade uranium dioxide powders and pellets

    E-Print Network [OSTI]

    American Society for Testing and Materials. Philadelphia

    2000-01-01

    1.1 This test method covers the determination of uranium and the oxygen to uranium atomic ratio in nuclear grade uranium dioxide powder and pellets. 1.2 This test method does not include provisions for preventing criticality accidents or requirements for health and safety. Observance of this test method does not relieve the user of the obligation to be aware of and conform to all international, national, or federal, state and local regulations pertaining to possessing, shipping, processing, or using source or special nuclear material. 1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. 1.4 This test method also is applicable to UO3 and U3O8 powder.

  6. Radical anionic versus neutral 2,2'-bipyridyl coordination in uranium complexes supported by amide and ketimide ligands.

    E-Print Network [OSTI]

    Diaconescu, PL; Cummins, CC

    2015-01-01

    the organometallic chemistry of uranium. The radical anionicof Chemistry 2012 Journal Name present 2.4(9) at the uraniumChemistry 2013 Since our initial examples, others have also reported bridging benzene or toluene uranium

  7. Radical anionic versus neutral 2,2'-bipyridyl coordination in uranium complexes supported by amide and ketimide ligands.

    E-Print Network [OSTI]

    Diaconescu, PL; Cummins, CC

    2015-01-01

    A series of 2,2’-bipyridyl uranium complexes shows that bipyor a neutral ligand such that uranium is in the +4 oxidationBipyridyl Coordination in Uranium Complexes Supported by

  8. Uranium diphosphonates templated by interlayer organic amines

    SciTech Connect (OSTI)

    Nelson, Anna-Gay D.; Alekseev, Evgeny V.; Institut fuer Kristallographie, RWTH Aachen University, D-52066 Aachen ; Albrecht-Schmitt, Thomas E.; Department of Chemistry and Biochemistry, University of Notre Dame, IN 46556 ; Ewing, Rodney C.

    2013-02-15

    The hydrothermal treatment of uranium trioxide and methylenediphosphonic acid with a variety of amines (2,2-dipyridyl, triethylenediamine, ethylenediamine, and 1,10-phenanthroline) at 200 Degree-Sign C results in the crystallization of a series of layered uranium diphosphonate compounds, [C{sub 10}H{sub 9}N{sub 2}]{l_brace}UO{sub 2}(H{sub 2}O)[CH{sub 2}(PO{sub 3})(PO{sub 3}H)]{r_brace} (Ubip2), [C{sub 6}H{sub 14}N{sub 2}]{l_brace}(UO{sub 2}){sub 2}[CH{sub 2}(PO{sub 3})(PO{sub 3}H)]{sub 2}{center_dot}2H{sub 2}O{r_brace} (UDAB), [C{sub 2}H{sub 10}N{sub 2}]{sub 2}{l_brace}(UO{sub 2}){sub 2}(H{sub 2}O){sub 2}[CH{sub 2}(PO{sub 3}){sub 2}]{sub 2}{center_dot}0.5H{sub 2}O{r_brace} (Uethyl), and [C{sub 12}H{sub 9}N{sub 2}]{l_brace}UO{sub 2}(H{sub 2}O)[CH{sub 2}(PO{sub 3})(PO{sub 3}H)]{r_brace} (Uphen). The crystal structures of the compounds are based on UO{sub 7} units linked by methylenediphosphonate molecules to form two-dimensional anionic sheets in Ubip2 and UDAB, and one-dimensional anionic chains in Uethyl and Uphen, which are charge balanced by protonated amine molecules. Interaction of the amine molecules with phosphonate oxygens and water molecules results in extensive hydrogen bonding in the interlayer. These amine molecules serve both as structure-directing agents and charge-balancing cations for the anionic uranium phosphonate sheets and chains in the formation of the different coordination geometries and topologies of each structure. Reported herein are the syntheses, structural and spectroscopic characterization of the synthesized compounds. - Graphical abstract: The Raman spectra of the synthesized compounds and an illustration of the stacking of the layers with the diprotonated triethylenediamine molecules in [C{sub 6}H{sub 14}N{sub 2}]{l_brace}(UO{sub 2}){sub 2}[CH{sub 2}(PO{sub 3})(PO{sub 3}H)]{sub 2}{center_dot}2H{sub 2}O{r_brace} UDAB. Solvent water molecules are removed for clarity. The corresponding Raman spectra for the complexes synthesized is also shown. The structure is constructed from UO{sub 7} pentagonal bipyramids (yellow), oxygen=red, phosphorus=magenta, carbon=black, and nitrogen=blue. Highlights: Black-Right-Pointing-Pointer Organic amines act both as charge-balancing and as structure-directing agents. Black-Right-Pointing-Pointer Extensive hydrogen bonding interactions with solvent water molecules and amines. Black-Right-Pointing-Pointer Altering the organic amine (size or flexibility) affects structure formation.

  9. Evaluation of Uranium Measurements in Water by Various Methods - 13571

    SciTech Connect (OSTI)

    Tucker, Brian J. [Shaw Environmental and Infrastructure Group, 150 Royall Street, Canton, MA (United States)] [Shaw Environmental and Infrastructure Group, 150 Royall Street, Canton, MA (United States); Workman, Stephen M. [ALS Laboratory Group, Environmental Division, 225 Commerce Drive, Fort Collins, CO 80524 (United States)] [ALS Laboratory Group, Environmental Division, 225 Commerce Drive, Fort Collins, CO 80524 (United States)

    2013-07-01

    In December 2000, EPA amended its drinking water regulations for radionuclides by adding a Maximum Contaminant Level (MCL) for uranium (so called MCL Rule)[1] of 30 micrograms per liter (?g/L). The MCL Rule also included MCL goals of zero for uranium and other radionuclides. Many radioactively contaminated sites must test uranium in wastewater and groundwater to comply with the MCL rule as well as local publicly owned treatment works discharge limitations. This paper addresses the relative sensitivity, accuracy, precision, cost and comparability of two EPA-approved methods for detection of total uranium: inductively plasma/mass spectrometry (ICP-MS) and alpha spectrometry. Both methods are capable of measuring the individual uranium isotopes U-234, U- 235, and U-238 and both methods have been deemed acceptable by EPA. However, the U-238 is by far the primary contributor to the mass-based ICP-MS measurement, especially for naturally-occurring uranium, which contains 99.2745% U-238. An evaluation shall be performed relative to the regulatory requirement promulgated by EPA in December 2000. Data will be garnered from various client sample results measured by ALS Laboratory in Fort Collins, CO. Data shall include method detection limits (MDL), minimum detectable activities (MDA), means and trends in laboratory control sample results, performance evaluation data for all methods, and replicate results. In addition, a comparison will be made of sample analyses results obtained from both alpha spectrometry and the screening method Kinetic Phosphorescence Analysis (KPA) performed at the U.S. Army Corps of Engineers (USACE) FUSRAP Maywood Laboratory (UFML). Many uranium measurements occur in laboratories that only perform radiological analysis. This work is important because it shows that uranium can be measured in radiological as well as stable chemistry laboratories and it provides several criteria as a basis for comparison of two uranium test methods. This data will indicate which test method is the most accurate and most cost effective. This paper provides a benefit to Formerly Utilized Sites Remedial Action Program (FUSRAP) and other Department of Defense (DOD) programs that may be performing uranium measurements. (authors)

  10. Microbiological, Geochemical and Hydrologic Processes Controlling Uranium Mobility: An Integrated Field Scale Subsurface Research Challenge Site at Rifle, Colorado, February 2011 to January 2012

    E-Print Network [OSTI]

    Long, P.E.

    2013-01-01

    Hasche-Berger, A. Eds. ), Uranium, Mining and Hydrogeology.Monitoring: A History of Uranium Mining and Processing in

  11. An Optically Stimulated Luminescence Uranium Enrichment Monitor

    SciTech Connect (OSTI)

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

    2010-08-11

    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).

  12. Interdiffusion and Reaction between Uranium and Iron

    SciTech Connect (OSTI)

    K. Huang; Y. Park; A. Ewh; B. H. Sencer; J. R. Kennedy; K. R. Coffey; Y. H. Sohn

    2012-05-01

    Metallic uranium alloy fuels cladded in stainless steel are being examined for fast reactors that operate at high temperature. In this work, solid-to-solid diffusion couples were assembled between pure U and Fe, and annealed at 853K, 888K and 923K where U exists as orthorhombic {alpha}, and at 953K and 973K where U exists as tetragonal {beta}. The microstructures and concentration profiles developed during annealing were examined by scanning electron microscopy and electron probe microanalysis, respectively. U{sub 6}Fe and UFe{sub 2} intermetallics developed in all diffusion couples, and U{sub 6}Fe was observed to grow faster than UFe{sub 2}. The interdiffusion fluxes of U and Fe were calculated to determine the integrated interdiffusion coefficients in U{sub 6}Fe and UFe{sub 2}. The extrinsic (K{sub I}) and intrinsic growth constants (K{sub II}) of U{sub 6}Fe and UFe{sub 2} were also calculated according to Wagner's formalism. The difference between K{sub I} and K{sub II} of UFe{sub 2} indicate that its growth was impeded by the fast-growing U{sub 6}Fe phase. However, the thin UFe{sub 2} played only a small role on the growth of U{sub 6}Fe as its K{sub I} and K{sub II} values were determined to be similar. The allotropic transformation of uranium (orthorhombic {alpha} to tetragonal {beta} phase) was observed to influence the growth of U{sub 6}Fe directly, because the growth rate of U{sub 6}Fe changed based on variation of activation energy. The change in chemical potential and crystal structure of U due to the allotropic transformation affected the interdiffusion between U and U{sub 6}Fe. Faster growth of U{sub 6}Fe is also examined with respect to various factors including crystal structure, phase diagram, and diffusion.

  13. Uranium- and thorium-bearing pegmatites of the United States

    SciTech Connect (OSTI)

    Adams, J.W.; Arengi, J.T.; Parrish, I.S.

    1980-04-01

    This report is part of the National Uranium Resource Evaluation (NURE) Program designed to identify criteria favorable for the occurrence of the world's significant uranium deposits. This project deals specifically with uranium- and thorium-bearing pegmatites in the United States and, in particular, their distribution and origin. From an extensive literature survey and field examination of 44 pegmatite localities in the United States and Canada, the authors have compiled an index to about 300 uranium- and thorium-bearing pegmatites in the United States, maps giving location of these deposits, and an annotated bibliography to some of the most pertinent literature on the geology of pegmatites. Pegmatites form from late-state magma differentiates rich in volatile constituents with an attendant aqueous vapor phase. It is the presence of an aqueous phase which results in the development of the variable grain size which characterizes pegmatites. All pegmatites occur in areas of tectonic mobility involving crustal material usually along plate margins. Those pegmatites containing radioactive mineral species show, essentially, a similar distribution to those without radioactive minerals. Criteria such as tectonic setting, magma composition, host rock, and elemental indicators among others, all serve to help delineate areas more favorable for uranium- and thorium-bearing pegmatites. The most useful guide remains the radioactivity exhibited by uranium- and thorium-bearing pegmatites. Although pegmatites are frequently noted as favorable hosts for radioactive minerals, the general paucity and sporadic distribution of these minerals and inherent mining and milling difficulties negate the resource potential of pegmatites for uranium and thorium.

  14. Thermodynamics of the Complexation of Uranium(VI) by oxalate in aqueous solution at 10-70oC

    E-Print Network [OSTI]

    Di Bernardo, Plinio

    2009-01-01

    O. Tochiyama in Chemical Thermodynamics of Compounds andUpdate on the Chemical Thermodynamics of Uranium, Neptunium,Thermodynamics of the Complexation of Uranium(VI) with

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

    E-Print Network [OSTI]

    Mcdonough, William F.

    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

  16. Recovery of Depleted Uranium Fragments from Soil

    SciTech Connect (OSTI)

    Farr, C.P.; Alecksen, T.J.; Heronimus, R.S.; Simonds, M.H.; Farrar, D.R.; Baker, K.R. [Environmental Restoration Group, Inc., Washington St. NE, Albuquerque, NM (United States); Miller, M.L. [Sandia National Laboratories, Albuquerque, NM (United States)

    2008-07-01

    A cost-effective method was demonstrated for recovering depleted uranium (DU) fragments from soil. A compacted clean soil pad was prepared adjacent to a pile of soil containing DU fragments. Soil from the contaminated pile was placed on the pad in three-inch lifts using conventional construction equipment. Each lift was scanned with an automatic scanning system consisting of an array of radiation detectors coupled to a detector positioning system. The data were downloaded into ArcGIS for data presentation. Areas of the pad exhibiting scaler counts above the decision level were identified as likely locations of DU fragments. The coordinates of these locations were downloaded into a PDA that was wirelessly connected to the positioning system. The PDA guided technicians to the locations where hand-held trowels and shovels were used to remove the fragments. After DU removal, the affected areas were re-scanned and the new data patched into the data base to replace the original data. This new data set along with soil sample results served as final status survey data. (authors)

  17. Fire testing of bare uranium hexafluoride cylinders

    SciTech Connect (OSTI)

    Pryor, W.A. [PAI Corp., Oak Ridge, TN (United States)

    1991-12-31

    In 1965, the Oak Ridge Gaseous Diffusion Plant (ORGDP), now the K-25 Site, conducted a series of tests in which bare cylinders of uranium hexafluoride (UF{sub 6}) were exposed to engulfing oil fires for the US Atomic Energy Commission (AEC), now the US Department of Energy (DOE). The tests are described and the results, conclusions, and observations are presented. Two each of the following types of cylinders were tested: 3.5-in.-diam {times} 7.5-in.-long cylinders of Monel (Harshaw), 5.0-in.-diam {times} x 30-in.-long cylinders of Monel, and 8-in.-diam {times} 48-in.-long cylinders of nickel. The cylinders were filled approximately to the standard UF{sub 6} fill limits of 5, 55, and 250 lb, respectively, with a U-235 content of 0.22%. The 5-in.- and 8-in.-diam cylinders were tested individually with and without their metal valve covers. For the 3.5-in.-diam Harshaw cylinders and the 5.0-in.-diam cylinder without a valve cover, the valves failed and UF{sub 6} was released. The remaining 6 cylinders ruptured explosively in time intervals ranging from about 8.5 to 11 min.

  18. Fire testing of bare uranium hexafluoride cylinders

    SciTech Connect (OSTI)

    Pryor, W.A. [PAI Corp., Oak Rige, TN (United States)

    1991-12-31

    In 1965, the Oak Ridge Gaseous Diffusion Plant (ORGDP), now the K-25 Site, conducted a series of tests in which bare cylinders of uranium hexafluoride (UF{sub 6}) were exposed to engulfing oil fires for the US Atomic Energy Commission (AEC), now the US Department of Energy (DOE). The tests are described and the results, conclusions, and observations are presented. Two each of the following types of cylinders were tested: 3.5-in.-diam {times} 7.5-in.-long cylinders of Monel (Harshaw), 5.0-in.-diam {times} 30-in.-long cylinders of Monel, and 8-in.-diam {times} 48-in.-long cylinders of nickel. The cylinders were filled approximately to the standard UF{sub 6} fill limits of 5, 55, and 250 lb, respectively, with a U-235 content of 0.22%. The 5-in.- and 8-in.-diam cylinders were tested individually with and without their metal valve covers. For the 3.5-in.-diam Harshaw cylinders and the 5.0-in.-diam cylinder without a valve cover the valves failed and UF{sub 6} was released. The remaining cylinders ruptured explosively in time intervals ranging from about 8.5 to 11 min.

  19. The solubility of uranium hexafluoride in perfluoroethers

    SciTech Connect (OSTI)

    Barber, E.J.

    1984-07-15

    The polyperfluoroethers are compatible with uranium hexafluoride (UF/sub 6/) and are suitable for use in diffusion pumps and in mechanical vacuum pumps which rely on oil as both the lubricant and the seal. The UF/sub 6/ is soluble in all fluids with which it is compatible. Because a number of vacuum pumps in the BOP facilities of the GCEP plant employ these perfluoroether oils as the working fluid and have oil chambers which are large, questions have been raised as to the relationships governing the solubility of UF/sub 6/ in these materials and the maximum quantities of UF/sub 6/ which could be dissolved in these oils under credible accident conditions. This report summarizes these solubility relations and the interaction of the UF/sub 6/ solubility and the pumping capability of this type of vacuum pump. It will be shown that, whereas the solubility of UF/sub 6/ in Fomblin Y25 fluoroether fluid under a UF/sub 6/ pressure of 760 torr and at the pump operating temperature of 160/sup 0/F is about 500 g of UF/sub 6/ per liter of oil, the system controls are such as to isolate the system from the pumps before the quantity of UF/sub 6/ dissolved in the perfluoroether exceeds about 10 g of UF/sub 6/ per liter of oil. 13 refs., 7 figs.

  20. Liquid uranium alloy-helium fission reactor

    DOE Patents [OSTI]

    Minkov, Vladimir (Skokie, IL)

    1986-01-01

    This invention teaches a nuclear fission reactor having a core vessel and at least one tandem heat exchanger vessel coupled therewith across upper and lower passages to define a closed flow loop. Nuclear fuel such as a uranium alloy in its liquid phase fills these vessels and flow passages. Solid control elements in the reactor core vessel are adapted to be adjusted relative to one another to control fission reaction of the liquid fuel therein. Moderator elements in the other vessel and flow passages preclude fission reaction therein. An inert gas such as helium is bubbled upwardly through the heat exchanger vessel operable to move the liquid fuel upwardly therein and unidirectionally around the closed loop and downwardly through the core vessel. This helium gas is further directed to heat conversion means outside of the reactor vessels to utilize the heat from the fission reaction to generate useful output. The nuclear fuel operates in the 1200.degree.-1800.degree. C. range, and even higher to 2500.degree. C., limited only by the thermal effectiveness of the structural materials, increasing the efficiency of power generation from the normal 30-35% with 300.degree.-500.degree. C. upper limit temperature to 50-65%. Irradiation of the circulating liquid fuel, as contrasted to only localized irradiation of a solid fuel, provides improved fuel utilization.

  1. Liquid uranium alloy-helium fission reactor

    DOE Patents [OSTI]

    Minkov, V.

    1984-06-13

    This invention describes a nuclear fission reactor which has a core vessel and at least one tandem heat exchanger vessel coupled therewith across upper and lower passages to define a closed flow loop. Nuclear fuel such as a uranium alloy in its liquid phase fills these vessels and flow passages. Solid control elements in the reactor core vessel are adapted to be adjusted relative to one another to control fission reaction of the liquid fuel therein. Moderator elements in the other vessel and flow passages preclude fission reaction therein. An inert gas such as helium is bubbled upwardly through the heat exchanger vessel operable to move the liquid fuel upwardly therein and unidirectionally around the closed loop and downwardly through the core vessel. This helium gas is further directed to heat conversion means outside of the reactor vessels to utilize the heat from the fission reaction to generate useful output. The nuclear fuel operates in the 1200 to 1800/sup 0/C range, and even higher to 2500/sup 0/C.

  2. Uranium Adsorption on Ion-Exchange Resins - Batch Testing

    SciTech Connect (OSTI)

    Mattigod, Shas V.; Golovich, Elizabeth C.; Wellman, Dawn M.; Cordova, Elsa A.; Smith, Ronald M.

    2010-12-01

    The uranium adsorption performance of five resins (Dowex 1, Dowex 21K 16-30 [fresh], Dowex 21K 16-30 [regenerated], Purofine PFA600/4740, and ResinTech SIR-1200) were tested using unspiked, nitrate-spiked, and nitrate-spiked/pH adjusted source water from well 299-W19-36. These batch tests were conducted in support of a resin selection process in which the best resin to use for uranium treatment in the 200-West Area groundwater pump-and-treat system will be identified. The results from these tests are as follows: • The data from the high-nitrate (1331 mg/L) tests indicated that Dowex 1, Dowex 21K 16-30 (fresh), Purofine PFA600/4740, and ResinTech SIR-1200 all adsorbed uranium similarly well with Kd values ranging from ~15,000 to 95,000 ml/g. All four resins would be considered suitable for use in the treatment system based on uranium adsorption characteristics. • Lowering the pH of the high nitrate test conditions from 8.2 to 7.5 did not significantly change the uranium adsorption isotherms for the four tested resins. The Kd values for these four resins under high nitrate (1338 mg/L), lower pH (7.5) ranged from ~15,000 to 80,000 ml/g. • Higher nitrate concentrations greatly reduced the uranium adsorption on all four resins. Tests conducted with unspiked (no amendments; nitrate at 337 mg/L and pH at 8.2) source water yielded Kd values for Dowex 1, Dowex 21K 16-30 (fresh), Purofine PFA600/4740, and ResinTech SIR-1200 resins ranging from ~800,000 to >3,000,000 ml/g. These values are about two orders of magnitude higher than the Kd values noted from tests conducted using amended source water. • Compared to the fresh resin, the regenerated Dowex 21K 16-30 resin exhibited significantly lower uranium-adsorption performance under all test conditions. The calculated Kd values for the regenerated resin were typically an order of magnitude lower than the values calculated for the fresh resin. • Additional testing using laboratory columns is recommended to better resolve differences between the adsorption abilities of the resins and to develop estimates of uranium loading on the resins. By determining the quantity of uranium that each resin can adsorb and the time required to reach various levels of loading, resin lifetime in the treatment system can be estimated.

  3. Impact of organic matter and speciation on the behaviour of uranium in submerged ultrafiltration 

    E-Print Network [OSTI]

    Semião, Andrea J.C.; Rossiter, Helfrid M.A.; Schäfer, Andrea

    2010-01-01

    Influence of organic matter (OM) on uranium removal mechanisms by ultrafiltration (UF) over a pH range of 3–11 was investigated. Humic, alginic and tannic acid were used as OM. It was found that uranium adsorbed strongly ...

  4. Multiconfigurational nature of 5f orbitals in uranium and plutonium intermetallics

    E-Print Network [OSTI]

    Booth, C. H.

    2014-01-01

    Orbitals in Uranium and Plutonium Intermetallics C. H. BoothAbstract: Uranium and plutonium’s 5f electrons are tenuouslyanomalous properties of ?-plutonium. Nature 446(7135):513.

  5. Remediation of Uranium-contaminated Groundwater by Sorption onto Hydroxyapatite Derived

    E-Print Network [OSTI]

    Clement, Prabhakar

    Remediation of Uranium-contaminated Groundwater by Sorption onto Hydroxyapatite Derived from of CFHA to remove uranium (U(VI)) from aqueous phase was investigated using both batch and column experi

  6. 2014 Review of the Potential Impact of DOE Excess Uranium Inventory...

    Office of Environmental Management (EM)

    4 Review of the Potential Impact of DOE Excess Uranium Inventory On the Commercial Markets 2014 Review of the Potential Impact of DOE Excess Uranium Inventory On the Commercial...

  7. EIS-0472: Uranium Leasing Program, Mesa, Montrose, and San Miguel Counties, Colorado

    Broader source: Energy.gov [DOE]

    This EIS evaluated the potential environmental impacts of management alternatives for DOE’s Uranium Leasing Program, under which DOE administers tracts of land in western Colorado for exploration, development, and the extraction of uranium and vanadium ores.

  8. Uranium-series isotope and thermal constraints on the rate and depth of silicic magma genesis

    E-Print Network [OSTI]

    Sandiford, Mike

    Uranium-series isotope and thermal constraints on the rate and depth of silicic magma genesis A Sciences, University of Durham, South Road, Durham DH1 3LE, UK Abstract: Uranium-series isotopes provide

  9. Management Controls over the Department of Energy's Uranium Leasing Program, OAS-M-08-05

    Broader source: Energy.gov [DOE]

    The Department of Energy's Uranium Leasing Program was established by the Atomic Energy Act of 1954 to develop a supply of domestic uranium to meet the nation's defense needs. Pursuant to the Act,...

  10. Bacterial influence on uranium oxidation reduction reactions : implications for environmental remediation and isotopic composition

    E-Print Network [OSTI]

    Mullen, Lisa Maureen

    2007-01-01

    The bacterial influence on the chemistry and speciation of uranium has some important impacts on the environment, and can be exploited usefully for the purposes of environmental remediation of uranium waste contamination. ...

  11. Moab Uranium Mill Tailings Cleanup Project Steps into Spotlight at International Meeting in Vienna

    Broader source: Energy.gov [DOE]

    VIENNA – The Moab Uranium Mill Tailings Remedial Action (UMTRA) Project has kept the United States at the forefront of characterization, remediation, and end-state reuse of uranium millsites around the world.

  12. Synthesis of Uranium Trichloride for the Pyrometallurgical Processing of Used Nuclear Fuel

    SciTech Connect (OSTI)

    B.R. Westphal; J.C. Price; R.D. Mariani

    2011-11-01

    The pyroprocessing of used nuclear fuel via electrorefining requires the continued addition of uranium trichloride to sustain operations. Uranium trichloride is utilized as an oxidant in the system to allow separation of uranium metal from the minor actinides and fission products. The inventory of uranium trichloride had diminished to a point that production was necessary to continue electrorefiner operations. Following initial experimentation, cupric chloride was chosen as a reactant with uranium metal to synthesize uranium trichloride. Despite the variability in equipment and charge characteristics, uranium trichloride was produced in sufficient quantities to maintain operations in the electrorefiner. The results and conclusions from several experiments are presented along with a set of optimized operating conditions for the synthesis of uranium trichloride.

  13. Decolonizing cartographies : sovereignty, territoriality, and maps of meaning in the uranium landscape

    E-Print Network [OSTI]

    Voyles, Traci Brynne

    2010-01-01

    the 1940s, when the Manhattan Project used uranium found inthe lead of the Manhattan Project and the AEC geologists andyears (prior to the Manhattan Project, uranium was largely

  14. Molecular uranates - laser synthesis of uranium oxide anions in the gas phase

    E-Print Network [OSTI]

    Marcalo, Joaquim

    2011-01-01

    readily from solutions of uranyl salts by reaction withstate of the uranium, a uranyl moiety may or may not be

  15. Decolonizing cartographies : sovereignty, territoriality, and maps of meaning in the uranium landscape

    E-Print Network [OSTI]

    Voyles, Traci Brynne

    2010-01-01

    July 16, 1979, a mill tailings pond upstream of the Churchthe UNC uranium mill tailings pond ran right through our

  16. Stratigraphy of the PB-1 well, Nopal I uranium deposit, Sierra Pena Blanca, Chihuahua, Mexico

    E-Print Network [OSTI]

    Dobson, P.

    2009-01-01

    2006, Paragenesis and geochronology of the Nopal I uranium1977, Subcommision on geochronology: Convention on the use

  17. Uranium Elemental and Isotopic Constraints on Groundwater Flow Beneath the Nopal I Uranium Deposit, Pena Blanca, Mexico

    SciTech Connect (OSTI)

    S.J. Goldstein; M.T. Murrell; A.M. Simmons

    2005-07-11

    The Nopal I uranium deposit in Chihuahua, Mexico, is an excellent analogue for evaluating the fate of spent fuel, associated actinides, and fission products over long time scales for the proposed Yucca Mountain high-level nuclear waste repository. In 2003, three groundwater wells were drilled directly adjacent to (PB-1) and 50 m on either side of the uranium deposit (PB-2 and PB-3) in order to evaluate uranium-series transport in three dimensions. After drilling, uranium concentrations were elevated in all of the three wells (0.1-18 ppm) due to drilling activities and subsequently decreased to {approx}5-20% of initial values over the next several months. The {sup 234}U/{sup 238}U activity ratios were similar for PB-1 and PB-2 (1.005 to 1.079) but distinct for PB-3 (1.36 to 1.83) over this time period, suggesting limited mixing between groundwater from these wells over these short time and length scales. Regional groundwater wells located up to several km from the deposit also have distinct uranium isotopic characteristics and constrain mixing over larger length and time scales. We model the decreasing uranium concentrations in the newly drilled wells with a simple one-dimensional advection-dispersion model, assuming uranium is introduced as a slug to each of the wells and transported as a conservative tracer. Using this model for our data, the relative uranium concentrations are dependent on both the longitudinal dispersion as well as the mean groundwater flow velocity. These parameters have been found to be correlated in both laboratory and field studies of groundwater velocity and dispersion (Klotz et al., 1980). Using typical relationships between velocity and dispersion for field and laboratory studies along with the relationship observed from our uranium data, both velocity (1-10 n/yr) and dispersion coefficient (1E-5 to 1E-2 cm{sup 2}/s) can be derived from the modeling. As discussed above, these relatively small flow velocities and dispersivities agree with mixing considerations derived from the {sup 234}U/{sup 238}U data. While these results and the limited productivity of these wells consistently suggest limited groundwater flow and mixing, we anticipate additional work with artificial tracers to better establish groundwater flow velocities and gradient at this site.

  18. DETERMINING OPTICAL CONSTANTS OF URANIUM NITRIDE THIN FILMS IN THE EXTREME

    E-Print Network [OSTI]

    Hart, Gus

    deposition and characterization of reactively-sputtered uranium nitride thin films. I also report opticalDETERMINING OPTICAL CONSTANTS OF URANIUM NITRIDE THIN FILMS IN THE EXTREME ULTRAVIOLET (1.6-35 NM.1 Application 1 1.2 Optical Constants 2 1.3 Project Focus 7 2 Uranium Nitride Thin Films 8 2.1 Sputtering 8 2

  19. Acoustic Measurements of the Elastic Properties and Quality of Plutonium and Uranium Based Oxide Fuels

    E-Print Network [OSTI]

    Acoustic Measurements of the Elastic Properties and Quality of Plutonium and Uranium Based Oxide ranged from depleted uranium oxide to mixtures of plutonium and depleted uranium oxide (MOX) and mixed.8Pu0.2 92 121 152.6 63.3 281Plutonium Futures -- The Science 2010, September 19-23, 2010, Keystone, CO

  20. Fermi Surface of Uranium at Ambient Pressure Gregory S. Boebinger, National High Magnetic Field Laboratory

    E-Print Network [OSTI]

    Weston, Ken

    Fermi Surface of ­Uranium at Ambient Pressure Gregory S. Boebinger, National High Magnetic Field Laboratory DMR-Award 0654118 DC Field Facility User Program The fermi surface of ­Uranium has been measured surface of alpha-uranium at ambient pressure, Phys. Rev. B Rapid Commun., 80, 241101 (2009). B//c-axis B

  1. Short Communication Bioreduction and precipitation of uranium in ionic liquid aqueous

    E-Print Network [OSTI]

    Ohta, Shigemi

    Short Communication Bioreduction and precipitation of uranium in ionic liquid aqueous solution by Clostridium sp. C. Zhang a,b, , C.J. Dodge c , S.V. Malhotra a,1 , A.J. Francis c,d a Department of Chemistry t s Uranium forms various complexes with ionic liquids. Uranium bioreduction was affected by the type

  2. FINITE ELEMENT IMPLEMENTATION OF A SELF-CONSISTENT POLYCRYSTAL PLASTICITY MODEL: APPLICATION TO -URANIUM

    E-Print Network [OSTI]

    Mihaila, Bogdan

    TO -URANIUM Marko Knezevic, Rodney J. McCabe, Ricardo A. Lebensohn, Carlos N. Tomé, and Bogdan Mihaila Keywords: Uranium; Constitutive modeling; Finite Element Method Abstract We present an improved mechanical response of wrought -uranium. In this regard, a finite element integration point is considered

  3. UserCalc: A Web-based uranium series calculator for magma migration problems

    E-Print Network [OSTI]

    Spiegelman, Marc W.

    UserCalc: A Web-based uranium series calculator for magma migration problems M. Spiegelman Lamont] Abstract: Measured departures from secular equilibrium in the uranium series decay chains provide important series models. Keywords: Uranium series disequilibrium; geochemical models; mantle modeling; magma

  4. Uranium in iron formations and the rise of atmospheric oxygen C.A. Partin a,

    E-Print Network [OSTI]

    Konhauser, Kurt

    Uranium in iron formations and the rise of atmospheric oxygen C.A. Partin a, , S.V. Lalonde b , N Paleoproterozoic Geochemical uranium cycle The concept of the Great Oxidation Event (GOE), during which atmospheric oxygenation through the record of uranium (U) concentrations in iron formations (IF). Just as IF are important

  5. Uranium Oxide as a Highly Reflective Coating from 150-350 eV

    E-Print Network [OSTI]

    Hart, Gus

    1 Uranium Oxide as a Highly Reflective Coating from 150-350 eV Richard L. Sandberg, David D. Allred.byu.edu ABSTRACT We present the measured reflectances (beamline 6.3.2, ALS at LBNL) of naturally oxidized uranium incidence. These show that uranium, as UO2, can fulfill its promise as the highest known single surface

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

    E-Print Network [OSTI]

    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 design has been carried out for the measurement of uranium enrichment using this technique with different

  7. INTERACTIONS OF 100 MeV/NUCLEON 40 Ar WITH URANIUM

    E-Print Network [OSTI]

    Frankel, Kenneth Alan

    2010-01-01

    100 MeV/nucleon " A r with Uranium D by Kenneth Alan Frankelc t i l e s w i t h a uranium t a r g e t have been measuredMeV/nucleon *° Argon + Uranium • Fragments (5 6 Z _ c l , <

  8. 2.0 GEOGRAPHIC ANALYSIS ON THE LOCATION OF URANIUM MINES

    E-Print Network [OSTI]

    2.0 GEOGRAPHIC ANALYSIS ON THE LOCATION OF URANIUM MINES With the exception of some phosphate mine areas in central and northern Florida, people are most likely to be exposed to uranium mining to understand the potential impacts and scenarios by which humans and the environment may be impacted by uranium

  9. Refinement in the ultrasonic velocity data and estimation of the critical parameters for molten uranium dioxide

    E-Print Network [OSTI]

    Azad, Abdul-Majeed

    uranium dioxide Abdul-Majeed Azad * Department of Chemical and Environmental Engineering, The University, reliable data on the sound prop- agation velocity in molten uranium dioxide have been obtained. An equation 61:98 ffiffiffiffi T p : ð1Þ For stoichiometric uranium oxide (O/U = 2.00) values of 3070 K [6], 3115

  10. ORNL/TM-2008/195 Model of a Generic Natural Uranium

    E-Print Network [OSTI]

    Pennycook, Steve

    ORNL/TM-2008/195 Model of a Generic Natural Uranium Conversion Plant--Suggested Measures OF A GENERIC NATURAL URANIUM CONVERSION PLANT-- SUGGESTED MEASURES TO STRENGTHEN INTERNATIONAL SAFEGUARD From ........................................................................................................................ 1 2. TECHNICAL PROCESS FOR NATURAL URANIUM CONVERSION PLANTS ...................... 2 2.1 Generic

  11. UserCalc: a web-based Uranium Series Calculator for magma migration problems

    E-Print Network [OSTI]

    Spiegelman, Marc W.

    UserCalc: a web-based Uranium Series Calculator for magma migration problems M. Spiegelman Lamont. Measured departures from secular equilibrium in the Uranium-series decay chains provide important-series models. Introduction Radioactive decay chains such as the two Uranium series 238 U230 Th226 Ra and 235 U

  12. Aerobic uranium (VI) bioprecipitation by metal-resistant bacteria isolated from radionuclide-

    E-Print Network [OSTI]

    Skolnick, Jeff

    Aerobic uranium (VI) bioprecipitation by metal-resistant bacteria isolated from radionuclide uranium [U(VI)] mediated by the intrinsic phosphatase acti- vities of naturally occurring bacteria such as uranium (U), technetium (Tc) and other toxic metals [e.g. cadmium (Cd), lead (Pb), chromium (Cr

  13. Uranium Watch 76 South Main Street, # 7 | P.O. Box 344

    E-Print Network [OSTI]

    Uranium Watch 76 South Main Street, # 7 | P.O. Box 344 Moab, Utah 84532 435-26O-8384, May 2, 2014. Dear Mr. Rosnick: REQUEST FOR EXTENSION OF TIME TO SUBMIT COMMENTS Uranium Watch requests Rosnick/EPA 2 June 10, 2014 1 http://www.radiationcontrol.utah.gov/Uranium_Mills/uraniumone/docs/2012

  14. CHAPTER 6. BIBLIOGRAPHY AAPG 2005--American Association of Petroleum Geologists. Recent Uranium Industry Developments,

    E-Print Network [OSTI]

    Industry Developments, Exploration, Mining and Environmental Programs in the U.S. and Overseas. Uranium-Solution Mining. Uranium 1 (1978): 37-52. Burghardt 2003--Burghardt. J. Capitol Reef National Park (Utah): Rainy Day and Duchess Uranium Mines-Site Characterization (September 2002) Summary results presented at U

  15. Multicomponent reactive transport modeling at the Ratones uranium mine, Cceres (Spain)

    E-Print Network [OSTI]

    Politècnica de Catalunya, Universitat

    Multicomponent reactive transport modeling at the Ratones uranium mine, Cáceres (Spain) Modelación management. The Ratones uranium mine was abandoned and flooded in 1974. Due to its reducing underground water, uranium, reactive transport, granite hydrochemistry, Ratones mine. Resumen La inundación de minas

  16. New Technique for Speciation of Uranium in Sediments Following Acetate-Stimulated Bioremediation

    SciTech Connect (OSTI)

    Not Available

    2011-06-22

    Acetate-stimulated bioremediation is a promising new technique for sequestering toxic uranium contamination from groundwater. The speciation of uranium in sediments after such bioremediation attempts remains unknown as a result of low uranium concentration, and is important to analyzing the stability of sequestered uranium. A new technique was developed for investigating the oxidation state and local molecular structure of uranium from field site sediments using X-Ray Absorption Spectroscopy (XAS), and was implemented at the site of a former uranium mill in Rifle, CO. Glass columns filled with bioactive Rifle sediments were deployed in wells in the contaminated Rifle aquifer and amended with a hexavalent uranium (U(VI)) stock solution to increase uranium concentration while maintaining field conditions. This sediment was harvested and XAS was utilized to analyze the oxidation state and local molecular structure of the uranium in sediment samples. Extended X-Ray Absorption Fine Structure (EXAFS) data was collected and compared to known uranium spectra to determine the local molecular structure of the uranium in the sediment. Fitting was used to determine that the field site sediments did not contain uraninite (UO{sub 2}), indicating that models based on bioreduction using pure bacterial cultures are not accurate for bioremediation in the field. Stability tests on the monomeric tetravalent uranium (U(IV)) produced by bioremediation are needed in order to assess the efficacy of acetate-stimulation bioremediation.

  17. Plutonium (III) and uranium (III) nitrile complexes

    SciTech Connect (OSTI)

    Enriquez, A. E.; Matonic, J. H.; Scott, B. L.; Neu, M. P.

    2002-01-01

    Iodine oxidation of uranium and plutonium metals in tetrahydrofuran and pyridine form AnI{sub 3}(THF){sub 4} and AnI{sub 3}(py){sub 4} (An = Pu, U). These compounds represent convenient entries Into solution An(III) chemistry in organic solvents. Extensions of the actinide metal oxidation methodology in nitrile solvents by I{sub 2}, AgPF{sub 6}, and TIPF{sub 6} are presented here. Treatment of Pu{sup 0} in acetonitrile with iodine yields a putative PuI{sub 3}(NCMe){sub x} intermediate which can be trapped with the tripodal nitrogen donor ligand tpza (tpza = (tris[(2-pyrazinyl)methyl]amine)) and forms the eight-coordinate complex (tpza)PuI{sub 3}(NCMe). Treatment of excess U{sup 0} metal by iodine in acetonitrile afforded a brown crystalline mixed valence complex, [U(NCMe){sub 9}][UI{sub 6}][I], instead of UI{sub 3}(NCMe){sub 4}. The analogous reaction in bezonitrile forms red crystalline UI{sub 4}(NCPh){sub 4}. In contrast, treatment of UI{sub 3}(THF){sub 4} with excess acetonitrile cleanly generates [U(NCMe){sub 9}][I]{sub 3}. Oxidation of Pu{sup 0} by either TI(I) or Ag(I) hexafluorophosphate salts generates a nine-coordinate homoleptic acetonitrile adduct [Pu(NCMe){sub 9}][PF{sub 6}]{sub 3}. Attempts to oxidize U{sub 0} with these salts were unsuccessful.

  18. Method for monitoring stack gases for uranium activity

    DOE Patents [OSTI]

    Beverly, Claude R. (Paducah, KY); Ernstberger, Harold G. (Paducah, KY)

    1988-01-01

    A method for monitoring the stack gases of a purge cascade of a gaseous diffusion plant for uranium activity. A sample stream is taken from the stack gases and contacted with a volume of moisture-laden air for converting trace levels of uranium hexafluoride, if any, in the stack gases into particulate uranyl fluoride. A continuous strip of filter paper from a supply roll is passed through this sampling stream to intercept and gather any uranyl fluoride in the sampling stream. This filter paper is then passed by an alpha scintillation counting device where any radioactivity on the filter paper is sensed so as to provide a continuous monitoring of the gas stream for activity indicative of the uranium content in the stack gases.

  19. Method for monitoring stack gases for uranium activity

    DOE Patents [OSTI]

    Beverly, C.R.; Ernstberger, E.G.

    1985-07-03

    A method for monitoring the stack gases of a purge cascade of gaseous diffusion plant for uranium activity. A sample stream is taken from the stack gases and contacted with a volume of moisture-laden air for converting trace levels of uranium hexafluoride, if any, in the stack gases into particulate uranyl fluoride. A continuous strip of filter paper from a supply roll is passed through this sampling stream to intercept and gather any uranyl fluoride in the sampling stream. This filter paper is then passed by an alpha scintillation counting device where any radioactivity on the filter paper is sensed so as to provide a continuous monitoring of the gas stream for activity indicative of the uranium content in the stack gases. 1 fig.

  20. Uranium Metal Reaction Behavior in Water, Sludge, and Grout Matrices

    SciTech Connect (OSTI)

    Delegard, Calvin H.; Schmidt, Andrew J.

    2008-09-25

    This report summarizes information and data on the reaction behavior of uranium metal in water, in water-saturated simulated and genuine K Basin sludge, and in grout matrices. This information and data are used to establish the technical basis for metallic uranium reaction behavior for the K Basin Sludge Treatment Project (STP). The specific objective of this report is to consolidate the various sources of information into a concise document to serve as a high-level reference and road map for customers, regulators, and interested parties outside the STP (e.g., external reviewers, other DOE sites) to clearly understand the current basis for the corrosion of uranium metal in water, sludge, and grout.