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Note: This page contains sample records for the topic "uranium oxide lb" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
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1

Method for converting uranium oxides to uranium metal  

DOE Patents [OSTI]

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

Duerksen, Walter K. (Norris, TN)

1988-01-01T23:59:59.000Z

2

CHARACTERIZATION OF URANIUM, URANIUM OXIDE AND SILICON MULTILAYER THIN FILMS  

E-Print Network [OSTI]

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

Hart, Gus

3

Influence of uranium hydride oxidation on uranium metal behaviour  

SciTech Connect (OSTI)

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

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

2013-07-01T23:59:59.000Z

4

Method for fluorination of uranium oxide  

DOE Patents [OSTI]

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.

Petit, George S. (Oak Ridge, TN)

1987-01-01T23:59:59.000Z

5

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]

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

American Society for Testing and Materials. Philadelphia

2008-01-01T23:59:59.000Z

6

Uranium Oxide Aerosol Transport in Porous Graphite  

SciTech Connect (OSTI)

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.

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.

2012-01-23T23:59:59.000Z

7

Ultrafiltration evaluation with depleted uranium oxide  

SciTech Connect (OSTI)

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

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

1998-03-01T23:59:59.000Z

8

Probing the Electronic Structures of Low Oxidation-State Uranium...  

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

Fluoride Molecules UFx- (x2-4). Probing the Electronic Structures of Low Oxidation-State Uranium Fluoride Molecules UFx- (x2-4). Abstract: We report the experimental observation...

9

Probing the electronic structures of low oxidation-state uranium...  

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

molecules UFx- (x2-4) . Probing the electronic structures of low oxidation-state uranium fluoride molecules UFx- (x2-4) . Abstract: We report the experimental observation...

10

Uranium Oxide as a Highly Reflective Coating from 150-350 eV  

E-Print Network [OSTI]

of depleted uranium metal (less than 0.2% U-235). After sputtering, the uranium was allowed to oxidize1 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

Hart, Gus

11

Standard specification for sintered gadolinium oxide-uranium dioxide pellets  

E-Print Network [OSTI]

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...

American Society for Testing and Materials. Philadelphia

2008-01-01T23:59:59.000Z

12

Pentavalent Uranium Chemistry - Synthetic Pursuit Of A Rare Oxidation State  

SciTech Connect (OSTI)

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.

Graves, Christopher R [Los Alamos National Laboratory; Kiplinger, Jaqueline L [Los Alamos National Laboratory

2009-01-01T23:59:59.000Z

13

Fundamental study on recovery uranium oxide from HEPA filters  

SciTech Connect (OSTI)

Large numbers of spent HEPA filters are produced at uranium fuel fabrication facilities. Uranium oxide particles have been collected on these filters. Then, a spent HEPA filter treatment system was developed from the viewpoint of recovering the UO{sub 2} and minimizing the volume. The system consists of a mechanical separation process and a chemical dissolution process. This paper describes the results of fundamental experiments on recovering UO{sub 2} from HEPA filters.

Izumida, T. [Hitachi Ltd., Ibaraki (Japan). Hitachi Works; Matsumoto, H.; Tsuchiya, H.; Iba, H. [Hitachi Nuclear Engineering Co., Ltd., Ibaraki (Japan); Noguchi, Y. [Radioactive Waste Management Center, Tokyo (Japan)

1993-12-31T23:59:59.000Z

14

Oxidation Protection of Uranium Nitride Fuel using Liquid Phase Sintering  

SciTech Connect (OSTI)

Two methods are proposed to increase the oxidation resistance of uranium nitride (UN) nuclear fuel. These paths are: (1) Addition of USi{sub x} (e.g. U3Si2) to UN nitride powder, followed by liquid phase sintering, and (2) 'alloying' UN nitride with various compounds (followed by densification via Spark Plasma Sintering or Liquid Phase Sintering) that will greatly increase oxidation resistance. The advantages (high thermal conductivity, very high melting point, and high density) of nitride fuel have long been recognized. The sodium cooled BR-10 reactor in Russia operated for 18 years on uranium nitride fuel (UN was used as the driver fuel for two core loads). However, the potential advantages (large power up-grade, increased cycle lengths, possible high burn-ups) as a Light Water Reactor (LWR) fuel are offset by uranium nitride's extremely low oxidation resistance (UN powders oxidize in air and UN pellets decompose in hot water). Innovative research is proposed to solve this problem and thereby provide an accident tolerant LWR fuel that would resist water leaks and high temperature steam oxidation/spalling during an accident. It is proposed that we investigate two methods to increase the oxidation resistance of UN: (1) Addition of USi{sub x} (e.g. U{sub 3}Si{sub 2}) to UN nitride powder, followed by liquid phase sintering, and (2) 'alloying' UN nitride with compounds (followed by densification via Spark Plasma Sintering) that will greatly increase oxidation resistance.

Dr. Paul A. Lessing

2012-03-01T23:59:59.000Z

15

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

Broader source: Energy.gov [DOE]

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

16

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

Broader source: Energy.gov [DOE]

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

17

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

SciTech Connect (OSTI)

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

NONE

1995-07-05T23:59:59.000Z

18

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

SciTech Connect (OSTI)

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

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

2013-02-01T23:59:59.000Z

19

Standard test methods for analysis of sintered gadolinium oxide-uranium dioxide pellets  

E-Print Network [OSTI]

1.1 These test methods cover procedures for the analysis of sintered gadolinium oxide-uranium dioxide pellets to determine compliance with specifications. 1.2 The analytical procedures appear in the following order: Section Carbon (Total) by Direct CombustionThermal Conductivity Method C1408 Test Method for Carbon (Total) in Uranium Oxide Powders and Pellets By Direct Combustion-Infrared Detection Method Chlorine and Fluorine by Pyrohydrolysis Ion-Selective Electrode Method C1502 Test Method for Determination of Total Chlorine and Fluorine in Uranium Dioxide and Gadolinium Oxide Gadolinia Content by Energy-Dispersive X-Ray Spectrometry C1456 Test Method for Determination of Uranium or Gadolinium, or Both, in Gadolinium Oxide-Uranium Oxide Pellets or by X-Ray Fluorescence (XRF) Hydrogen by Inert Gas Fusion C1457 Test Method for Determination of Total Hydrogen Content of Uranium Oxide Powders and Pellets by Carrier Gas Extraction Isotopic Uranium Composition by Multiple-Filament Surface-Ioni...

American Society for Testing and Materials. Philadelphia

2006-01-01T23:59:59.000Z

20

Standard test method for carbon (total) in uranium oxide powders and pellets by direct combustion-infrared detection method  

E-Print Network [OSTI]

Standard test method for carbon (total) in uranium oxide powders and pellets by direct combustion-infrared detection method

American Society for Testing and Materials. Philadelphia

2009-01-01T23:59:59.000Z

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


21

Preparation and Characterization of Uranium Oxides in Support of the K Basin Sludge Treatment Project  

SciTech Connect (OSTI)

Uraninite (UO2) and metaschoepite (UO3·2H2O) are the uranium phases most frequently observed in K Basin sludge. Uraninite arises from the oxidation of uranium metal by anoxic water and metaschoepite arises from oxidation of uraninite by atmospheric or radiolytic oxygen. Studies of the oxidation of uraninite by oxygen to form metaschoepite were performed at 21°C and 50°C. A uranium oxide oxidation state characterization method based on spectrophotometry of the solution formed by dissolving aqueous slurries in phosphoric acid was developed to follow the extent of reaction. This method may be applied to determine uranium oxide oxidation state distribution in K Basin sludge. The uraninite produced by anoxic corrosion of uranium metal has exceedingly fine particle size (6 nm diameter), forms agglomerates, and has the formula UO2.004±0.007; i.e., is practically stoichiometric UO2. The metaschoepite particles are flatter and wider when prepared at 21°C than the particles prepared at 50°C. These particles are much smaller than the metaschoepite observed in prolonged exposure of actual K Basin sludge to warm moist oxidizing conditions. The uraninite produced by anoxic uranium metal corrosion and the metaschoepite produced by reaction of uraninite aqueous slurries with oxygen may be used in engineering and process development testing. A rapid alternative method to determine uranium metal concentrations in sludge also was identified.

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

2008-07-08T23:59:59.000Z

22

Molten salt extraction of transuranic and reactive fission products from used uranium oxide fuel  

DOE Patents [OSTI]

Used uranium oxide fuel is detoxified by extracting transuranic and reactive fission products into molten salt. By contacting declad and crushed used uranium oxide fuel with a molten halide salt containing a minor fraction of the respective uranium trihalide, transuranic and reactive fission products partition from the fuel to the molten salt phase, while uranium oxide and non-reactive, or noble metal, fission products remain in an insoluble solid phase. The salt is then separated from the fuel via draining and distillation. By this method, the bulk of the decay heat, fission poisoning capacity, and radiotoxicity are removed from the used fuel. The remaining radioactivity from the noble metal fission products in the detoxified fuel is primarily limited to soft beta emitters. The extracted transuranic and reactive fission products are amenable to existing technologies for group uranium/transuranic product recovery and fission product immobilization in engineered waste forms.

Herrmann, Steven Douglas

2014-05-27T23:59:59.000Z

23

Importance of atmospheric inputs and Fe-oxides in controlling soil uranium budgets and behavior along a Hawaiian chronosequence  

E-Print Network [OSTI]

Importance of atmospheric inputs and Fe-oxides in controlling soil uranium budgets and behavior: D. Rickard Abstract A long-term budget of uranium calculated for a chronosequence of Hawaiian soils extractions on the same soils shows a strong association between Fe-oxides and uranium, especially

Derry, Louis A.

24

Uranium Extraction From Laboratory Synthesized, Uranium-Doped Hydrous Ferric Oxides  

SciTech Connect (OSTI)

The extractability of uranium (U) from synthetic hydrous ferric oxides has been shown to decrease as a function of mineral ripening, consistent with the hypothesis that the ripening process decrease contaminant lability. To evaluate this process, three hydrous ferric oxide (HFO) suspensions were co-precipitated with uranyl (UO22+) and maintained at pH 7.0 ± 0.1. Uranyl was added to the HFO post-precipitation in a fourth suspension. Two suspensions also contained either co-precipitated silicate (Si-U-HFO) or phosphate (P-U-HFO). After precipitation of the HFOs, at time intervals of one week, one month, six months, one year, and 2 years, aliquots of the suspensions were contacted with five solutions for a range of time. The extracts were analyzed for U and iron (Fe). The results are consistent with the hypothesis that U and Fe extractability will decrease as the mineral phase ripens. All extracting solutions exhibited some degree of selectivity for U, as the proportional extraction of U exceeded that for congruent dissolution. Micro X-ray diffraction analysis indicates the transformation from an amorphous phase to a material containing substantial proportions of crystalline goethite and hematite, except the P-U-HFO which remained primarily amorphous. Further analysis of the co-precipitates by the Mössbauer technique and scanning electron microscopy (SEM) provides further evidence of mineralogic ripening

Smith, Steven C.; Douglas, Matthew; Moore, Dean A.; Kukkadapu, Ravi K.; Arey, Bruce W.

2009-03-01T23:59:59.000Z

25

A comparison of two lung clearance models based on the dissolution rates of oxidized depleted uranium  

E-Print Network [OSTI]

by Cuddihy. Predictions fr'om bai. h models based on the dissolution rates of the amount of oxidized depleted uranium that wau'ld be cleared to blood irom the pu lraana ry region i'o'i)owing an i nba !at i cn exposure were compared . It was f:urd ti... to oxidized depleted uranium (DU) aerosol. The ob, ject. ive of th. is i:hesis was three fold: (1) to determine the dissolution rates for two respirable DU samples, (2) to determine the specific pulmonary clearance characteristics of oxidized DU, (3) Co...

Crist, Kevin Craig

1983-01-01T23:59:59.000Z

26

Purification of uranium alloys by differential solubility of oxides and production of purified fuel precursors  

DOE Patents [OSTI]

A method is described for purifying metallic alloys of uranium for use as nuclear reactor fuels in which the metal alloy is first converted to an oxide and then dissolved in nitric acid. Initial removal of metal oxide impurities not soluble in nitric acid is accomplished by filtration or other physical means. Further purification can be accomplished by carbonate leaching of uranyl ions from the partially purified solution or using traditional methods such as solvent extraction. 3 figs.

McLean, W. II; Miller, P.E.

1997-12-16T23:59:59.000Z

27

Purification of uranium alloys by differential solubility of oxides and production of purified fuel precursors  

DOE Patents [OSTI]

A method for purifying metallic alloys of uranium for use as nuclear reactor fuels in which the metal alloy is first converted to an oxide and then dissolved in nitric acid. Initial removal of metal oxide impurities not soluble in nitric acid is accomplished by filtration or other physical means. Further purification can be accomplished by carbonate leaching of uranyl ions from the partially purified solution or using traditional methods such as solvent extraction.

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

1997-01-01T23:59:59.000Z

28

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

Broader source: Energy.gov [DOE]

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

29

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

Broader source: Energy.gov [DOE]

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

30

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

Broader source: Energy.gov [DOE]

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

31

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

Broader source: Energy.gov [DOE]

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

32

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

Broader source: Energy.gov [DOE]

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

33

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

Broader source: Energy.gov [DOE]

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

34

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

Broader source: Energy.gov [DOE]

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

35

Author's personal copy Microbial reduction of chlorite and uranium followed by air oxidation  

E-Print Network [OSTI]

Author's personal copy Microbial reduction of chlorite and uranium followed by air oxidation, University Park, PA, USA c Department of Geological and Environmental Sciences, University of Akron, Akron, OH, USA d Department of Geology, Miami University, Oxford, OH, USA e Biosciences Division, Argonne

Burgos, William

36

EIS-0089: PUREX Plant and Uranium Oxide Plant Facilities, Hanford Site, Richland, Washington  

Broader source: Energy.gov [DOE]

The U.S. Department of Energy developed this statement to evaluate the environmental impacts of resumption of operations of the PUREX/Uranium Oxide facilities at the Hanford Site to produce plutonium and other special nuclear materials for national defense needs.

37

Standard specification for uranium oxides with a 235U content of less than 5 % for dissolution prior to conversion to nuclear-grade uranium dioxide  

E-Print Network [OSTI]

1.1 This specification covers uranium oxides, including processed byproducts or scrap material (powder, pellets, or pieces), that are intended for dissolution into uranyl nitrate solution meeting the requirements of Specification C788 prior to conversion into nuclear grade UO2 powder with a 235U content of less than 5 %. This specification defines the impurity and uranium isotope limits for such urania powders that are to be dissolved prior to processing to nuclear grade UO2 as defined in Specification C753. 1.2 This specification provides the nuclear industry with a general standard for such uranium oxide powders. It recognizes the diversity of conversion processes and the processes to which such powders are subsequently to be subjected (for instance, by solvent extraction). It is therefore anticipated that it may be necessary to include supplementary specification limits by agreement between the buyer and seller. 1.3 The scope of this specification does not comprehensively cover all provisions for prevent...

American Society for Testing and Materials. Philadelphia

2005-01-01T23:59:59.000Z

38

Observations of Oxygen Ion Behavior in the Lithium-Based Electrolytic Reduction of Uranium Oxide  

SciTech Connect (OSTI)

Parametric studies were performed on a lithium-based electrolytic reduction process at bench-scale to investigate the behavior of oxygen ions in the reduction of uranium oxide for various electrochemical cell configurations. Specifically, a series of eight electrolytic reduction runs was performed in a common salt bath of LiCl – 1 wt% Li2O. The variable parameters included fuel basket containment material (i.e., stainless steel wire mesh and sintered stainless steel) and applied electrical charge (i.e., 75 – 150% of the theoretical charge for complete reduction of uranium oxide in a basket to uranium metal). Samples of the molten salt electrolyte were taken at regular intervals throughout each run and analyzed to produce a time plot of Li2O concentrations in the bulk salt over the course of the runs. Following each run, the fuel basket was sectioned and the fuel was removed. Samples of the fuel were analyzed for the extent of uranium oxide reduction to metal and for the concentration of salt constituents, i.e., LiCl and Li2O. Extents of uranium oxide reduction ranged from 43 – 70% in stainless steel wire mesh baskets and 8 – 33 % in sintered stainless steel baskets. The concentrations of Li2O in the salt phase of the fuel product from the stainless steel wire mesh baskets ranged from 6.2 – 9.2 wt%, while those for the sintered stainless steel baskets ranged from 26 – 46 wt%. Another series of tests was performed to investigate the dissolution of Li2O in LiCl at 650 °C across various cathode containment materials (i.e., stainless steel wire mesh, sintered stainless steel and porous magnesia) and configurations (i.e., stationary and rotating cylindrical baskets). Dissolution of identical loadings of Li2O particulate reached equilibrium within one hour for stationary stainless steel wire mesh baskets, while the same took several hours for sintered stainless steel and porous magnesia baskets. Rotation of an annular cylindrical basket of stainless steel wire mesh accelerated the Li2O dissolution rate by more than a factor of six.

Steven D. Herrmann; Shelly X. Li; Brenda E. Serrano-Rodriguez

2009-09-01T23:59:59.000Z

39

Uranium Immobilization through Fe(II) bio-oxidation: A Column study  

SciTech Connect (OSTI)

Current research on the bioremediation of heavy metals and radionuclides is focused on the ability of reducing organisms to use these metals as alternative electron acceptors in the absence of oxygen and thus precipitate them out of solution. However, many aspects of this proposed scheme need to be resolved, not the least of which is the time frame of the treatment process. Once treatment is complete and the electron donor addition is halted, the system will ultimately revert back to an oxic state and potentially result in the abiotic reoxidation and remobilization of the immobilized metals. In addition, the possibility exists that the presence of more electropositive electron acceptors such as nitrate or oxygen will also stimulate the biological oxidation and remobilization of these contaminants. The selective nitrate-dependent biooxidation of added Fe(II) may offer an effective means of “capping off” and completing the attenuation of these contaminants in a reducing environment making the contaminants less accessible to abiotic and biotic reactions and allowing the system to naturally revert to an oxic state. Our previous DOE-NABIR funded studies demonstrated that radionuclides such as uranium and cobalt are rapidly removed from solution during the biogenic formation of Fe(III)-oxides. In the case of uranium, X-ray spectroscopy analysis indicated that the uranium was in the hexavalent form (normally soluble) and was bound to the precipitated Fe(III)-oxides thus demonstrating the bioremediative potential of this process. We also demonstrated that nitrate-dependent Fe(II)- oxidizing bacteria are prevalent in the sediment and groundwater samples collected from sites 1 and 2 and the background site of the NABIR FRC in Oakridge, TN. However, all of these studies were performed in batch experiments in the laboratory with pure cultures and although a significant amount was learned about the microbiology of nitrate-dependent bio-oxidation of Fe(II), the effects of complex processes (such as advective flow) present in the natural environment are unknown. The objective of the current studies was to address some of these short-comings in an attempt to develop this bioremediative strategy into a robust, field applicable technology. This objective was approached by both pure culture studies investigating the mechanism of Fe(II) oxidation by nitrate reducing bacteria and examining the flow dynamics and microbial processes in advective flow columns amended with Fe(II) and nitrate over an extended period.

Coates, John D.

2009-09-14T23:59:59.000Z

40

Criticality experiments with mixed oxide fuel pin arrays in plutonium-uranium nitrate solution  

SciTech Connect (OSTI)

A series of critical experiments was completed with mixed plutonium-uranium solutions having a Pu/(Pu + U) ratio of approximately 0.22 in a boiler tube-type lattice assembly. These experiments were conducted as part of the Criticality Data Development Program between the United States Department of Energy (USDOE) and the Power Reactor and Nuclear Fuel Development Corporation (PNC) of Japan. A complete description of the experiments and data are included in this report. The experiments were performed with an array of mixed oxide fuel pins in aqueous plutonium-uranium solutions. The fuel pins were contained in a boiler tube-type tank and arranged in a 1.4 cm square pitch array which resembled cylindrical geometry. One experiment was perfomed with the fuel pins removed from the vessel. The experiments were performed with a water reflector. The concentration of the solutions in the boiler tube-type tank was varied from 4 to 468 g (Pu + U)/liter. The ratio of plutonium to total heavy metal (plutonium plus uranium) was approximately 0.22 for all experiments.

Lloyd, R.C. (Pacific Northwest Lab., Richland, WA (United States)); Smolen, G.R. (Oak Ridge National Lab., TN (United States))

1988-08-01T23:59:59.000Z

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


41

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

E-Print Network [OSTI]

uranium budgets and behavior along a Hawaiian chronosequence. Chemical GeologyUranium isotopic evidence for the origin of the Bahariya iron deposits, Egypt. Ore Geology

Stewart, B.D.

2009-01-01T23:59:59.000Z

42

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

E-Print Network [OSTI]

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

Stewart, B.D.

2009-01-01T23:59:59.000Z

43

Fire hazards analysis for the uranium oxide (UO{sub 3}) facility  

SciTech Connect (OSTI)

The Fire Hazards Analysis (FHA) documents the deactivation end-point status of the UO{sub 3} complex fire hazards, fire protection and life safety systems. This FHA has been prepared for the Uranium Oxide Facility by Westinghouse Hanford Company in accordance with the criteria established in DOE 5480.7A, Fire Protection and RLID 5480.7, Fire Protection. The purpose of the Fire Hazards Analysis is to comprehensively and quantitatively assess the risk from a fire within individual fire areas in a Department of Energy facility so as to ascertain whether the objectives stated in DOE Order 5480.7, paragraph 4 are met. Particular attention has been paid to RLID 5480.7, Section 8.3, which specifies the criteria for deactivating fire protection in decommission and demolition facilities.

Wyatt, D.M.

1994-12-06T23:59:59.000Z

44

Process for electrolytically preparing uranium metal  

DOE Patents [OSTI]

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

Haas, Paul A. (Knoxville, TN)

1989-01-01T23:59:59.000Z

45

Bacterial influence on uranium oxidation reduction reactions : implications for environmental remediation and isotopic composition  

E-Print Network [OSTI]

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. ...

Mullen, Lisa Maureen

2007-01-01T23:59:59.000Z

46

Survey of Worldwide Light Water Reactor Experience with Mixed Uranium-Plutonium Oxide Fuel  

SciTech Connect (OSTI)

The US and the Former Soviet Union (FSU) have recently declared quantities of weapons materials, including weapons-grade (WG) plutonium, excess to strategic requirements. One of the leading candidates for the disposition of excess WG plutonium is irradiation in light water reactors (LWRs) as mixed uranium-plutonium oxide (MOX) fuel. A description of the MOX fuel fabrication techniques in worldwide use is presented. A comprehensive examination of the domestic MOX experience in US reactors obtained during the 1960s, 1970s, and early 1980s is also presented. This experience is described by manufacturer and is also categorized by the reactor facility that irradiated the MOX fuel. A limited summary of the international experience with MOX fuels is also presented. A review of MOX fuel and its performance is conducted in view of the special considerations associated with the disposition of WG plutonium. Based on the available information, it appears that adoption of foreign commercial MOX technology from one of the successful MOX fuel vendors will minimize the technical risks to the overall mission. The conclusion is made that the existing MOX fuel experience base suggests that disposition of excess weapons plutonium through irradiation in LWRs is a technically attractive option.

Cowell, B.S.; Fisher, S.E.

1999-02-01T23:59:59.000Z

47

Method of preparation of uranium nitride  

DOE Patents [OSTI]

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

Kiplinger, Jaqueline Loetsch; Thomson, Robert Kenneth James

2013-07-09T23:59:59.000Z

48

ELECTRONIC SOLUTION SPECTRA FOR URANIUM AND NEPTUNIUM IN OXIDATION STATES (III) TO (VI) IN ANHYDROUS HYDROGEN FLUORIDE  

SciTech Connect (OSTI)

Spectra have been recorded for solutions in anhydrous hydrogen fluoride (AHF) of uranium and neptunium in oxidation states (III) to (VI). The spectra for U(III), Np(III) and Np(IV) in AHF are very similar to those in acidified aqueous solution, but that for U(IV) suggests that the cationic species is UF{sub 2}{sup 2+}. The AHF spectra for the elements in oxidation states (V) and (VI) are not comparable with those of the formally analogous aqueous solutions, where the elements exist as well-defined dioxo-cations. However, the AHF spectra can be related to spectra in the gas phase, in the solid state or in non-aqueous solvents for each element in its appropriate oxidation state.

Baluka, M.; Edelstein, N.; O'Donnell, T. A.

1980-10-01T23:59:59.000Z

49

Atomistic Simulations of Uranium Incorporation into Iron (Hydr...  

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

of Uranium Incorporation into Iron (Hydr)Oxides. Atomistic Simulations of Uranium Incorporation into Iron (Hydr)Oxides. Abstract: Atomistic simulations were carried out to...

50

Process for continuous production of metallic uranium and uranium alloys  

DOE Patents [OSTI]

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

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

1995-06-06T23:59:59.000Z

51

Process for continuous production of metallic uranium and uranium alloys  

DOE Patents [OSTI]

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

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

1995-01-01T23:59:59.000Z

52

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

SciTech Connect (OSTI)

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.

Ade, Brian J [ORNL; Gauld, Ian C [ORNL

2011-10-01T23:59:59.000Z

53

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

Broader source: Energy.gov [DOE]

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

54

Dissolution of metal oxides and separation of uranium from lanthanides and actinides in supercritical carbon dioxide  

SciTech Connect (OSTI)

This paper investigates the feasibility of extracting and separating uranium from lanthanides and other actinides by using supercritical fluid carbon dioxide (sc-CO{sub 2}) as a solvent modified with tri-n-butylphosphate (TBP) for the development of a counter current stripping technique, which would be a more efficient and environmentally benign technology for spent nuclear fuel reprocessing compared to traditional solvent extraction. Several actinides (U, Pu, and Np) and europium were extracted in sc-CO{sub 2} modified with TBP over a range of nitric acid concentrations and then the actinides were exposed to reducing and complexing agents to suppress their extractability. According to this study, uranium/europium and uranium/plutonium extraction and separation in sc-CO{sub 2} modified with TBP is successful at nitric acid concentrations of less than 6 M and at nitric acid concentrations of less than 3 M with acetohydroxamic acid or oxalic acid, respectively. A scheme for recycling uranium from spent nuclear fuel by using sc-CO{sub 2} and counter current stripping columns is presented. (authors)

Quach, D.L.; Wai, C.M. [Department of Chemistry, University of Idaho, Moscow, Idaho 83844 (United States); Mincher, B.J. [Idaho National Lab, Idaho Falls, Idaho (United States)

2013-07-01T23:59:59.000Z

55

DISSOLUTION OF METAL OXIDES AND SEPARATION OF URANIUM FROM LANTHANIDES AND ACTINIDES IN SUPERCRITICAL CARBON DIOXIDE  

SciTech Connect (OSTI)

This paper investigates the feasibility of extracting and separating uranium from lanthanides and other actinides by using supercritical fluid carbon dioxide (sc-CO2) as a solvent modified with tri-n-butylphosphate (TBP) for the development of a counter current stripping technique, which would be a more efficient and environmentally benign technology for spent nuclear fuel reprocessing compared to traditional solvent extraction. Several actinides (U, Pu, and Np) and europium were extracted in sc-CO2 modified with TBP over a range of nitric acid concentrations and then the actinides were exposed to reducing and complexing agents to suppress their extractability. According to this study, uranium/europium and uranium/plutonium extraction and separation in sc-CO2 modified with TBP is successful at nitric acid concentrations of less than 6 M and at nitric acid concentrations of less than 3 M with acetohydroxamic acid or oxalic acid, respectively. A scheme for recycling uranium from spent nuclear fuel by using sc-CO2 and counter current stripping columns is presented.

Donna L. Quach; Bruce J. Mincher; Chien M. Wai

2013-10-01T23:59:59.000Z

56

Uranium dioxide electrolysis  

DOE Patents [OSTI]

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

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

2009-12-29T23:59:59.000Z

57

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

Broader source: Energy.gov [DOE]

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

58

Method for the recovery of uranium values from uranium tetrafluoride  

DOE Patents [OSTI]

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

Kreuzmann, Alvin B. (Cincinnati, OH)

1983-01-01T23:59:59.000Z

59

Method for the recovery of uranium values from uranium tetrafluoride  

DOE Patents [OSTI]

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

Kreuzmann, A.B.

1982-10-27T23:59:59.000Z

60

A coupled transport and solid mechanics formulation with improved reaction kinetics parameters for modeling oxidation and decomposition in a uranium hydride bed.  

SciTech Connect (OSTI)

Modeling of reacting flows in porous media has become particularly important with the increased interest in hydrogen solid-storage beds. An advanced type of storage bed has been proposed that utilizes oxidation of uranium hydride to heat and decompose the hydride, releasing the hydrogen. To reduce the cost and time required to develop these systems experimentally, a valid computational model is required that simulates the reaction of uranium hydride and oxygen gas in a hydrogen storage bed using multiphysics finite element modeling. This SAND report discusses the advancements made in FY12 (since our last SAND report SAND2011-6939) to the model developed as a part of an ASC-P&EM project to address the shortcomings of the previous model. The model considers chemical reactions, heat transport, and mass transport within a hydride bed. Previously, the time-varying permeability and porosity were considered uniform. This led to discrepancies between the simulated results and experimental measurements. In this work, the effects of non-uniform changes in permeability and porosity due to phase and thermal expansion are accounted for. These expansions result in mechanical stresses that lead to bed deformation. To describe this, a simplified solid mechanics model for the local variation of permeability and porosity as a function of the local bed deformation is developed. By using this solid mechanics model, the agreement between our reacting bed model and the experimental data is improved. Additionally, more accurate uranium hydride oxidation kinetics parameters are obtained by fitting the experimental results from a pure uranium hydride oxidation measurement to the ones obtained from the coupled transport-solid mechanics model. Finally, the coupled transport-solid mechanics model governing equations and boundary conditions are summarized and recommendations are made for further development of ARIA and other Sandia codes in order for them to sufficiently implement the model.

Salloum, Maher N.; Shugard, Andrew D.; Kanouff, Michael P.; Gharagozloo, Patricia E.

2013-03-01T23:59:59.000Z

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


61

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

62

LB CRAC Workshops (rates/meetings)  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: VegetationEquipment Surfaces and Interfaces Sample Environment: Magnet and6 th LAPDLoad-Based (LB) CRAC

63

Uranium immobilization and nuclear waste  

SciTech Connect (OSTI)

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

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

1982-02-01T23:59:59.000Z

64

Uranium hexafluoride handling. Proceedings  

SciTech Connect (OSTI)

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

Not Available

1991-12-31T23:59:59.000Z

65

MASS AND DENSITY 1 kg = 2.2046 lb 1 lb = 0.4536 kg  

E-Print Network [OSTI]

.m = 0.73756 ft.lbf 1 ft.lbf = 1.35582 J 1 kJ = 737.56 ft.lbf 1 Btu = 778.17 ft.lbf 1 kJ = 0.9478 Btu 1 Btu = 1.0551 kJ 1 kJ/kg = 0.42992 Btu/lb 1 Btu/lb = 2.326 kJ/kg 1 kcal = 4.1868 kJ ENERGY TRANSFER RATE 1 W = 1 J/s = 3.413 Btu/h 1 Btu/h = 0.293 W 1kW = 1.341 hp 1 hp =2545 Btu/h 1 hp = 550 ft.lbf/s 1

Kostic, Milivoje M.

66

Pulsed DD Neutron Generator Measurements for HEU Oxide Fuel Pins Using Liquid Scintillators with Pulse Shape Discrimination  

E-Print Network [OSTI]

measurements have been performed on high-enriched uranium (HEU) oxide fuel pins and depleted uranium metal

Pennycook, Steve

67

Inherently safe in situ uranium recovery  

DOE Patents [OSTI]

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.

Krumhansl, James L; Brady, Patrick V

2014-04-29T23:59:59.000Z

68

Engineering assessment of inactive uranium mill tailings  

SciTech Connect (OSTI)

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

Not Available

1981-07-01T23:59:59.000Z

69

E-Print Network 3.0 - actinide doped uranium Sample Search Results  

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

dissolution rate in oxidizing... media is increasing all the more the content of uranium is increases in the mixed oxide. While for Th Source: Ecole Polytechnique, Centre...

70

Subsurface Uranium Fate and Transport: Integrated Experiments and Modeling of Coupled Biogeochemical Mechanisms of Nanocrystalline Uraninite Oxidation by Fe(III)-(hydr)oxides - Project Final Report  

SciTech Connect (OSTI)

Subsurface bacteria including sulfate reducing bacteria (SRB) reduce soluble U(VI) to insoluble U(IV) with subsequent precipitation of UO2. We have shown that SRB reduce U(VI) to nanometer-sized UO2 particles (1-5 nm) which are both intra- and extracellular, with UO2 inside the cell likely physically shielded from subsequent oxidation processes. We evaluated the UO2 nanoparticles produced by Desulfovibrio desulfuricans G20 under growth and non-growth conditions in the presence of lactate or pyruvate and sulfate, thiosulfate, or fumarate, using ultrafiltration and HR-TEM. Results showed that a significant mass fraction of bioreduced U (35-60%) existed as a mobile phase when the initial concentration of U(VI) was 160 µM. Further experiments with different initial U(VI) concentrations (25 - 900 ?M) in MTM with PIPES or bicarbonate buffers indicated that aggregation of uraninite depended on the initial concentrations of U(VI) and type of buffer. It is known that under some conditions SRB-mediated UO2 nanocrystals can be reoxidized (and thus remobilized) by Fe(III)-(hydr)oxides, common constituents of soils and sediments. To elucidate the mechanism of UO2 reoxidation by Fe(III) (hydr)oxides, we studied the impact of Fe and U chelating compounds (citrate, NTA, and EDTA) on reoxidation rates. Experiments were conducted in anaerobic batch systems in PIPES buffer. Results showed EDTA significantly accelerated UO2 reoxidation with an initial rate of 9.5?M day-1 for ferrihydrite. In all cases, bicarbonate increased the rate and extent of UO2 reoxidation with ferrihydrite. The highest rate of UO2 reoxidation occurred when the chelator promoted UO2 and Fe(III) (hydr)oxide dissolution as demonstrated with EDTA. When UO2 dissolution did not occur, UO2 reoxidation likely proceeded through an aqueous Fe(III) intermediate as observed for both NTA and citrate. To complement to these laboratory studies, we collected U-bearing samples from a surface seep at the Rifle field site and have measured elevated U concentrations in oxic iron-rich sediments. To translate experimental results into numerical analysis of U fate and transport, a reaction network was developed based on Sani et al. (2004) to simulate U(VI) bioreduction with concomitant UO2 reoxidation in the presence of hematite or ferrihydrite. The reduction phase considers SRB reduction (using lactate) with the reductive dissolution of Fe(III) solids, which is set to be microbially mediated as well as abiotically driven by sulfide. Model results show the oxidation of HS– by Fe(III) directly competes with UO2 reoxidation as Fe(III) oxidizes HS– preferentially over UO2. The majority of Fe reduction is predicted to be abiotic, with ferrihydrite becoming fully consumed by reaction with sulfide. Predicted total dissolved carbonate concentrations from the degradation of lactate are elevated (log(pCO2) ~ –1) and, in the hematite system, yield close to two orders-of-magnitude higher U(VI) concentrations than under initial carbonate concentrations of 3 mM. Modeling of U(VI) bioreduction with concomitant reoxidation of UO2 in the presence of ferrihydrite was also extended to a two-dimensional field-scale groundwater flow and biogeochemically reactive transport model for the South Oyster site in eastern Virginia. This model was developed to simulate the field-scale immobilization and subsequent reoxidation of U by a biologically mediated reaction network.

Peyton, Brent M. [Montana State University; Timothy, Ginn R. [University of California Davis; Sani, Rajesh K. [South Dakota School of Mines and Technology

2013-08-14T23:59:59.000Z

71

Uranium industry annual 1997  

SciTech Connect (OSTI)

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

NONE

1998-04-01T23:59:59.000Z

72

URANIUM IN ALKALINE ROCKS  

E-Print Network [OSTI]

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

Murphy, M.

2011-01-01T23:59:59.000Z

73

Method for fabricating laminated uranium composites  

DOE Patents [OSTI]

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.

Chapman, L.R.

1983-08-03T23:59:59.000Z

74

High pressure studies on uranium and thorium silicide compounds: Experiment S. Yagoubi a,b,c,  

E-Print Network [OSTI]

High pressure studies on uranium and thorium silicide compounds: Experiment and theory S. Yagoubi a, USi3, as well as some non-stoichiometric phases presented in Table 1. Among the thoriumB-type) that a ferromagnetic ordering is reported, with TC = 127 K and a saturated moment of 0.1 lB [3]. Concerning the thorium

Svane, Axel Torstein

75

Creation Date: August 8, 2013 Version: 1 Edited by: Application Services -LB ITS Managed Document  

E-Print Network [OSTI]

Creation Date: August 8, 2013 Version: 1 Edited by: Application Services - LB ITS Managed Document Date: August 8, 2013 Version: 1 Edited by: Application Services - LB ITS Managed Document PASSWORD

Northern British Columbia, University of

76

Uranium Metal Analysis via Selective Dissolution  

SciTech Connect (OSTI)

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.

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

2008-09-10T23:59:59.000Z

77

Creation Date: December, 2013 Version: 1 Edited by: LB Application Services -ITS Managed Document 1  

E-Print Network [OSTI]

Creation Date: December, 2013 Version: 1 Edited by: LB Application Services - ITS Managed Document". #12;Creation Date: December, 2013 Version: 1 Edited by: LB Application Services - ITS Managed Document Version: 1 Edited by: LB Application Services - ITS Managed Document 3 Forwarding Your UNBC Email

Northern British Columbia, University of

78

Creation Date: Mar 2014 Version: 1 Edited by: LB Application Services ITS Managed Document  

E-Print Network [OSTI]

Creation Date: Mar 2014 Version: 1 Edited by: LB Application Services ITS Managed Document VIEW Date: Mar 2014 Version: 1 Edited by: LB Application Services ITS Managed Document VIEW CLIENT Date: Mar 2014 Version: 1 Edited by: LB Application Services ITS Managed Document VIEW CLIENT

Northern British Columbia, University of

79

Disposition of Depleted Uranium Oxide  

SciTech Connect (OSTI)

This document summarizes environmental information which has been collected up to June 1983 at Savannah River Plant. Of particular interest is an updating of dose estimates from changes in methodology of calculation, lower cesium transport estimates from Steel Creek, and new sports fish consumption data for the Savannah River. The status of various permitting requirements are also discussed.

Crandall, J.L.

2001-08-13T23:59:59.000Z

80

Uranium industry annual 1996  

SciTech Connect (OSTI)

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

NONE

1997-04-01T23:59:59.000Z

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


81

Table 1. Canola 2010 large-plot variety and systems trial at Roseau. Yield, Lb/Acre at Test Wt, Lb/Bu at  

E-Print Network [OSTI]

Table 1. Canola 2010 large-plot variety and systems trial at Roseau. Yield, Lb/Acre at Test Wt, Lb Ready, LL = LibertyLink and CL = Clearfield. 51 Varietal Trials Results Canola Canola (Brassica napus and B. rapa) is a crop developed from oilseed rape by Canadian plant breeders; the first canola variety

Thomas, David D.

82

Scrap uranium recycling via electron beam melting  

SciTech Connect (OSTI)

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.

McKoon, R.

1993-11-01T23:59:59.000Z

83

Electrolytic process for preparing uranium metal  

DOE Patents [OSTI]

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.

Haas, Paul A. (Knoxville, TN)

1990-01-01T23:59:59.000Z

84

Capstone Depleted Uranium Aerosols: Generation and Characterization  

SciTech Connect (OSTI)

In a study designed to provide an improved scientific basis for assessing possible health effects from inhaling depleted uranium (DU) aerosols, a series of DU penetrators was fired at an Abrams tank and a Bradley fighting vehicle. A robust sampling system was designed to collect aerosols in this difficult environment and continuously monitor the sampler flow rates. Aerosols collected were analyzed for uranium concentration and particle size distribution as a function of time. They were also analyzed for uranium oxide phases, particle morphology, and dissolution in vitro. The resulting data provide input useful in human health risk assessments.

Parkhurst, MaryAnn; Szrom, Fran; Guilmette, Ray; Holmes, Tom; Cheng, Yung-Sung; Kenoyer, Judson L.; Collins, John W.; Sanderson, T. Ellory; Fliszar, Richard W.; Gold, Kenneth; Beckman, John C.; Long, Julie

2004-10-19T23:59:59.000Z

85

Uranium Industry Annual, 1992  

SciTech Connect (OSTI)

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

Not Available

1993-10-28T23:59:59.000Z

86

Using flow through reactors to study the non-reductive biomineralization of uranium phosphate minerals.  

E-Print Network [OSTI]

??Uranium contaminations of the subsurface in the vicinity of nuclear materials processing sites pose a health risk as the uranyl ion in its oxidized state,… (more)

Williams, Anna Rachel

2012-01-01T23:59:59.000Z

87

Creation Date: Feb 2014 Version: 1 Edited by: LB Application Services ITS Managed Document  

E-Print Network [OSTI]

Creation Date: Feb 2014 Version: 1 Edited by: LB Application Services ITS Managed Document VIEW: LB Application Services ITS Managed Document VIEW CLIENT INSTALLATION - MICROSOFT FEB 2014 STUDENT Managed Document VIEW CLIENT INSTALLATION - MICROSOFT FEB 2014 STUDENT Page 3 Virtual Desktop Login

Northern British Columbia, University of

88

Uranium industry annual 1994  

SciTech Connect (OSTI)

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

NONE

1995-07-05T23:59:59.000Z

89

Uranium-contaminated soils: Ultramicrotomy and electron beam analysis  

SciTech Connect (OSTI)

Uranium contaminated soils from the Fernald Operation Site, Ohio, have been examined by a combination of optical microscopy, scanning electron microscopy with backscattered electron detection (SEM/BSE), and analytical electron microscopy (AEM). A method is described for preparing of transmission electron microscopy (TEM) thin sections by ultramicrotomy. By using these thin sections, SEM and TEM images can be compared directly. Uranium was found in iron oxides, silicates (soddyite), phosphates (autunites), and fluorite. Little uranium was associated with clays. The distribution of uranium phases was found to be inhomogeneous at the microscopic level.

Buck, E.C.; Dietz, N.L.; Bates, J.K.; Cunnane, J.C.

1994-04-01T23:59:59.000Z

90

3-D Finite Element Electromagnetic and Stress Analyses of the JET LB-SRP Divertor Element (Tungsten Lamella Design)  

E-Print Network [OSTI]

3-D Finite Element Electromagnetic and Stress Analyses of the JET LB-SRP Divertor Element (Tungsten Lamella Design)

91

Depleted uranium disposal options evaluation  

SciTech Connect (OSTI)

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

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

1994-05-01T23:59:59.000Z

92

Electron Backscatter Diffraction (EBSD) Characterization of Uranium and Uranium Alloys  

SciTech Connect (OSTI)

Electron backscatter diffraction (EBSD) was used to examine the microstructures of unalloyed uranium, U-6Nb, U-10Mo, and U-0.75Ti. For unalloyed uranium, we used EBSD to examine the effects of various processes on microstructures including casting, rolling and forming, recrystallization, welding, and quasi-static and shock deformation. For U-6Nb we used EBSD to examine the microstructural evolution during shape memory loading. EBSD was used to study chemical homogenization in U-10Mo, and for U-0.75Ti, we used EBSD to study the microstructure and texture evolution during thermal cycling and deformation. The studied uranium alloys have significant microstructural and chemical differences and each of these alloys presents unique preparation challenges. Each of the alloys is prepared by a sequence of mechanical grinding and polishing followed by electropolishing with subtle differences between the alloys. U-6Nb and U-0.75Ti both have martensitic microstructures and both require special care in order to avoid mechanical polishing artifacts. Unalloyed uranium has a tendency to rapidly oxidize when exposed to air and a two-step electropolish is employed, the first step to remove the damaged surface layer resulting from the mechanical preparation and the second step to passivate the surface. All of the alloying additions provide a level of surface passivation and different one and two step electropolishes are employed to create good EBSD surfaces. Because of its low symmetry crystal structure, uranium exhibits complex deformation behavior including operation of multiple deformation twinning modes. EBSD was used to observe and quantify twinning contributions to deformation and to examine the fracture behavior. Figure 1 shows a cross section of two mating fracture surfaces in cast uranium showing the propensity of deformation twinning and intergranular fracture largely between dissimilarly oriented grains. Deformation of U-6Nb in the shape memory regime occurs by the motion of twin boundaries formed during the martensitic transformation. Deformation actually results in a coarsening of the microstructure making EBSD more practical following a limited amount of strain. Figure 2 shows the microstructure resulting from 6% compression. Casting of U-10Mo results in considerable chemical segregation as is apparent in Figure 2a. The segregation subsists through rolling and heat treatment processes as shown in Figure 2b. EBSD was used to study the effects of homogenization time and temperature on chemical heterogeneity. It was found that times and temperatures that result in a chemically homogeneous microstructure also result in a significant increase in grain size. U-0.75Ti forms an acicular martinsite as shown in Figure 4. This microstructure prevails through cycling into the higher temperature solid uranium phases.

McCabe, Rodney J. [Los Alamos National Laboratory; Kelly, Ann Marie [Los Alamos National Laboratory; Clarke, Amy J. [Los Alamos National Laboratory; Field, Robert D. [Los Alamos National Laboratory; Wenk, H. R. [University of California, Berkeley

2012-07-25T23:59:59.000Z

93

Selective Extraction of Uranium from Liquid or Supercritical Carbon Dioxide  

SciTech Connect (OSTI)

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

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

2012-07-31T23:59:59.000Z

94

Final Uranium Leasing Program Programmatic Environmental Impact...  

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

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

95

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

96

Mechanism of biosynthesis of the dimanganese-tyrosyl radical cofactor of class lb Ribonucleotide reductase  

E-Print Network [OSTI]

Ribonucleotide reductases (RNRs) catalyze the reduction of nucleotides to deoxynucleotides in all organisms. The class Ia and lb RNRs comprise two subunits: a2 contains the site of nucleotide reduction, and p2 contains an ...

Cotruvo, Joseph Alfred, Jr

2012-01-01T23:59:59.000Z

97

Depleted uranium: A DOE management guide  

SciTech Connect (OSTI)

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.

NONE

1995-10-01T23:59:59.000Z

98

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

E-Print Network [OSTI]

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

Hart, Gus

99

New Technique for Speciation of Uranium in Sediments Following Acetate-Stimulated Bioremediation  

SciTech Connect (OSTI)

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.

Not Available

2011-06-22T23:59:59.000Z

100

Synthesis of Uranium Trichloride for the Pyrometallurgical Processing of Used Nuclear Fuel  

SciTech Connect (OSTI)

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.

B.R. Westphal; J.C. Price; R.D. Mariani

2011-11-01T23:59:59.000Z

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


101

Welding of uranium and uranium alloys  

SciTech Connect (OSTI)

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

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

1982-03-26T23:59:59.000Z

102

EPA Update: NESHAP Uranium Activities  

E-Print Network [OSTI]

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

103

Uranium hexafluoride public risk  

SciTech Connect (OSTI)

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

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

1994-08-01T23:59:59.000Z

104

Depleted uranium hexafluoride: Waste or resource?  

SciTech Connect (OSTI)

the US Department of Energy is evaluating technologies for the storage, disposal, or re-use of depleted uranium hexafluoride (UF{sub 6}). This paper discusses the following options, and provides a technology assessment for each one: (1) conversion to UO{sub 2} for use as mixed oxide duel, (2) conversion to UO{sub 2} to make DUCRETE for a multi-purpose storage container, (3) conversion to depleted uranium metal for use as shielding, (4) conversion to uranium carbide for use as high-temperature gas-cooled reactor (HTGR) fuel. In addition, conversion to U{sub 3}O{sub 8} as an option for long-term storage is discussed.

Schwertz, N.; Zoller, J.; Rosen, R.; Patton, S. [Lawrence Livermore National Lab., CA (United States); Bradley, C. [USDOE Office of Nuclear Energy, Science, Technology, Washington, DC (United States); Murray, A. [SAIC (United States)

1995-07-01T23:59:59.000Z

105

Uranium Mill Tailings Management  

SciTech Connect (OSTI)

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

Nelson, J.D.

1982-01-01T23:59:59.000Z

106

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

SciTech Connect (OSTI)

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

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

2007-07-01T23:59:59.000Z

107

advanced oxidation process: Topics by E-print Network  

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

new tools for nuclear forensic science to facilitate the identification of chemical process history in uranium oxides. Nuclear forensics (more) Plaue, Jonathan 2013-01-01...

108

advanced oxidation processes: Topics by E-print Network  

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

new tools for nuclear forensic science to facilitate the identification of chemical process history in uranium oxides. Nuclear forensics (more) Plaue, Jonathan 2013-01-01...

109

actinide mixed oxide: Topics by E-print Network  

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

Nuclear fuel devices of Pressurised Water Reactors are composed of uranium oxide pellets which is correlated to an oxygen mass gain. From these experiments, we deduce the...

110

Preparation of uranium compounds  

DOE Patents [OSTI]

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

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

2013-02-19T23:59:59.000Z

111

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

E-Print Network [OSTI]

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

Winfree, Erik

112

Uranium industry annual 1993  

SciTech Connect (OSTI)

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

Not Available

1994-09-01T23:59:59.000Z

113

Porous membrane electrochemical cell for uranium and transuranic recovery from molten salt electrolyte  

DOE Patents [OSTI]

An improved process and device for the recovery of the minor actinides and the transuranic elements (TRU's) from a molten salt electrolyte. The process involves placing the device, an electrically non-conducting barrier between an anode salt and a cathode salt. The porous barrier allows uranium to diffuse between the anode and cathode, yet slows the diffusion of uranium ions so as to cause depletion of uranium ions in the catholyte. This allows for the eventual preferential deposition of transuranics present in spent nuclear fuel such as Np, Pu, Am, Cm. The device also comprises an uranium oxidation anode. The oxidation anode is solid uranium metal in the form of spent nuclear fuel. The spent fuel is placed in a ferric metal anode basket which serves as the electrical lead or contact between the molten electrolyte and the anodic uranium metal.

Willit, James L. (Ratavia, IL)

2007-09-11T23:59:59.000Z

114

Porous membrane electrochemical cell for uranium and transuranic recovery from molten salt electrolyte  

DOE Patents [OSTI]

An improved process and device for the recovery of the minor actinides and the transuranic elements (TRU's) from a molten salt electrolyte. The process involves placing the device, an electrically non-conducting barrier between an anode salt and a cathode salt. The porous barrier allows uranium to diffuse between the anode and cathode, yet slows the diffusion of uranium ions so as to cause depletion of uranium ions in the catholyte. This allows for the eventual preferential deposition of transuranics present in spent nuclear fuel such as Np, Pu, Am, Cm. The device also comprises an uranium oxidation anode. The oxidation anode is solid uranium metal in the form of spent nuclear fuel. The spent fuel is placed in a ferric metal anode basket which serves as the electrical lead or contact between the molten electrolyte and the anodic uranium metal.

Willit, James L. (Batavia, IL)

2010-09-21T23:59:59.000Z

115

WISE Uranium Project - Fact Sheet  

E-Print Network [OSTI]

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

Hazards From Depleted

116

India's Worsening Uranium Shortage  

SciTech Connect (OSTI)

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

Curtis, Michael M.

2007-01-15T23:59:59.000Z

117

Ionic Liquids as templating agents in formation of uranium-containing nanomaterials  

SciTech Connect (OSTI)

A method for forming nanoparticles containing uranium oxide is described. The method includes combining a uranium-containing feedstock with an ionic liquid to form a mixture and holding the mixture at an elevated temperature for a period of time to form the product nanoparticles. The method can be carried out at low temperatures, for instance less than about 300.degree. C.

Visser, Ann E; Bridges, Nicholas J

2014-06-10T23:59:59.000Z

118

Depleted uranium management alternatives  

SciTech Connect (OSTI)

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

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

1994-08-01T23:59:59.000Z

119

A New Look at Natural Humics on Uranium Stability and Mobility Humic substances naturally forming organic materials in soil and groundwater, have  

E-Print Network [OSTI]

A New Look at Natural Humics on Uranium Stability and Mobility Humic substances ­ naturally forming are significant because humics could present a potential challenge to immobilizing and stabilizing reduced uranium uranium bioreduction and oxidation. Environ. Sci. Technol. (in press). #12;

120

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

SciTech Connect (OSTI)

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

Sarychev, Michael; /Fermilab

2011-09-21T23:59:59.000Z

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


121

Uranium-contaminated soils: Ultramicrotomy and electron beam analysis  

SciTech Connect (OSTI)

Uranium-contaminated soils from the U.S. Department of Energy (DOE) Fernald Site, Ohio, have been examined by a combination of scanning electron microscopy with backscattered electron imaging (SEM/BSE) and analytical electron microscopy (AEM). The inhomogeneous distribution of particulate uranium phases in the soil required the development of a method for using ultramicrotomy to prepare transmission electron microscopy (TEM) thin sections of the SEM mounts. A water-miscible resin was selected that allowed comparison between SEM and TEM images, permitting representative sampling of the soil. Uranium was found in iron oxides, silicates (soddyite), phosphates (autunites), and fluorite (UO{sub 2}). No uranium was detected in association with phyllosilicates in the soil.

Buck, E.C.; Dietz, N.L.; Bates, J.K.; Cunnane, J.C.

1994-02-01T23:59:59.000Z

122

Fire testing of bare uranium hexafluoride cylinders  

SciTech Connect (OSTI)

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.

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

1991-12-31T23:59:59.000Z

123

Fire testing of bare uranium hexafluoride cylinders  

SciTech Connect (OSTI)

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.

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

1991-12-31T23:59:59.000Z

124

Mineralogical analysis and uranium distribution of the sediments from the upper Jackson formation, Karnes County, Texas  

E-Print Network [OSTI]

of the relationship between uranium distribu- tion and mineralogic composition of the sediment may provide more reliable methods for uranium exploration. Open pit mining and subsequent milling, or in situ leach- ing, are the two methods of uranium recovery... of the oxidized deposits, at and directly above the water table, are larger deposits of generally lower-grade ore that contains unoxidized uranium. The Galen Mine was the first mine in the unoxidized ore. This open pit mine is about two miles (3 km) south...

Fishman, Paul Harold

1978-01-01T23:59:59.000Z

125

XPS Determination of Uranium Oxidations States. | EMSL  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear SecurityTensile Strain Switched FerromagnetismWaste and MaterialsWenjun1ofRadiative Heating in

126

Uranium Enrichment Decontamination and Decommissioning Fund's...  

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

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

127

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

DOE Patents [OSTI]

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

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

1995-05-02T23:59:59.000Z

128

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

DOE Patents [OSTI]

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

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

1995-01-01T23:59:59.000Z

129

Controlling uranium reactivity March 18, 2008  

E-Print Network [OSTI]

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

Meyer, Karsten

130

Spatial and Geochemical Spatial and Geochemical Heterogeneity Impacts on Iron Biomineralization and Uranium Sequestration  

SciTech Connect (OSTI)

Bioreductive transformations of iron (hydr)oxides are a critically important processes controlling the fate and transport of contaminants in soil and aquifer systems. Heterogeneity arising from both chemical and physical conditions will lead to various biomineralization products of iron oxides and will additionally alter reactions controlling the partitioning of hazardous elements such as uranium. We are presently exploring chemical and mineralogical transformations within physically complex material having a range of pore-size distribution and chemical environments. Here we discuss the impact of calcium on the reactive transport of uranium and the spatial heterogeneity in iron hydroxide mineralization and concomitant uranium reduction along a diffusive flow path.

Scott Fendorf; Shawn Benner; Jim Neiss; Colleen Hansel; Peter Nico; Chris Francis; Phil Jardine

2004-03-17T23:59:59.000Z

131

Analytical Electron Microscopy examination of uranium contamination at the DOE Fernald operation site  

SciTech Connect (OSTI)

Analytical Electron Microscopy (AEM) has been used to identify uranium-bearing phases present in contaminated soils from the DOE Fernald operation site. A combination of optical microscopy, scanning electron microscopy with backscattered electron detection (SEM/BSE), and AEM was used in isolating and characterizing uranium-rich regions of the contaminated soils. Soil samples were prepared for transmission electron microscopy (TEM) by ultramicrotomy using an embedding resin previously employed for aquatic colloids and biological samples. This preparation method allowed direct comparison between SEM and TEM images. At the macroscopic level much of the uranium appears to be associated with clays in the soils; however, electron beam analysis revealed that the uranium is present as discrete phases, including iron oxides, silicates (soddyite), phosphates (autunites), and fluorite. Only low levels of uranium were actually within the clay minerals. The distribution of uranium phases was inhomogeneous at the submicron level.

Buck, E.C.; Dietz, N.L.; Bates, J.K.; Cunnane, J.C.

1993-02-01T23:59:59.000Z

132

Assessment of Preferred Depleted Uranium Disposal Forms  

SciTech Connect (OSTI)

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.

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

2000-06-01T23:59:59.000Z

133

Corrosion of aluminum-uranium alloys in water vapor at 200 C  

SciTech Connect (OSTI)

Specimens of aluminum-uranium alloys at 10 and 18 wt.% uranium were exposed to a saturated water vapor condition at 200 C up to about 12 weeks and compared to previous results for aluminum 1100. The aluminum-uranium materials exhibited a range of initial corrosion rates and approached similar rates with the formation of a passive film of boehmite (Al{sub 2}O{sub 3}{center{underscore}dot}H{sub 2}O). The initial corrosion rates of the aluminum-uranium materials were one to four times higher than that for aluminum 1100. It is postulated that a micro-galvanic coupling between the large UAl{sub 4} particles and the aluminum matrix has caused this difference. Sectioning the exposed specimens shows different characteristics of the oxide layers. In the oxide on the aluminum-10% uranium alloy (Al-10%U), small uranium aluminide particles can be seen in a boehmite matrix and do not seem to be corroded. The oxide film on the aluminum-18% uranium alloy (Al-18%U) appears to have two distinct oxide layers. The outer layer has mass aggregates in a boehmite matrix, while the inner layer contains UAl{sub 4} particles as in the case of Al-10%U.

Lam, P.S.; Sindelar, R.L.; Barrett, K.Y.

1999-07-01T23:59:59.000Z

134

Uranium-titanium-niobium alloy  

DOE Patents [OSTI]

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

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

1990-01-01T23:59:59.000Z

135

Uranium deposits of Brazil  

SciTech Connect (OSTI)

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

NONE

1991-09-01T23:59:59.000Z

136

Corrosion-resistant uranium  

DOE Patents [OSTI]

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

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

1981-10-21T23:59:59.000Z

137

Corrosion-resistant uranium  

DOE Patents [OSTI]

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

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

1983-01-01T23:59:59.000Z

138

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

139

The IMCA: A field instrument for uranium enrichment measurements  

SciTech Connect (OSTI)

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

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

1996-12-31T23:59:59.000Z

140

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

SciTech Connect (OSTI)

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

none,

1981-10-01T23:59:59.000Z

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


141

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

SciTech Connect (OSTI)

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

none,

1981-09-01T23:59:59.000Z

142

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

SciTech Connect (OSTI)

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

none,

1981-09-01T23:59:59.000Z

143

High loading uranium fuel plate  

DOE Patents [OSTI]

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

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

1990-01-01T23:59:59.000Z

144

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

SciTech Connect (OSTI)

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

Forsberg, C.W.

1997-02-19T23:59:59.000Z

145

Uranium from seawater  

SciTech Connect (OSTI)

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

Gregg, D.; Folkendt, M.

1982-09-21T23:59:59.000Z

146

URANIUM MILLING ACTIVITIES AT SEQUOYAH FUELS CORPORATION  

E-Print Network [OSTI]

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

unknown authors

147

Method for fabricating uranium foils and uranium alloy foils  

DOE Patents [OSTI]

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

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

2006-09-05T23:59:59.000Z

148

Method for providing uranium with a protective copper coating  

DOE Patents [OSTI]

The present invention is directed to a method for providing uranium metal with a protective coating of copper. Uranium metal is subjected to a conventional cleaning operation wherein oxides and other surface contaminants are removed, followed by etching and pickling operations. The copper coating is provided by first electrodepositing a thin and relatively porous flash layer of copper on the uranium in a copper cyanide bath. The resulting copper-layered article is then heated in an air or inert atmosphere to volatilize and drive off the volatile material underlying the copper flash layer. After the heating step an adherent and essentially non-porous layer of copper is electro-deposited on the flash layer of copper to provide an adherent, multi-layer copper coating which is essentially impervious to corrosion by most gases.

Waldrop, Forrest B. (Powell, TN); Jones, Edward (Knoxville, TN)

1981-01-01T23:59:59.000Z

149

Economics of nuclear fuel cycles : option valuation and neutronics simulation of mixed oxide fuels  

E-Print Network [OSTI]

In most studies aiming at the economic assessment of nuclear fuel cycles, a primary concern is to keep scenarios economically comparable. For Uranium Oxide (UOX) and Mixed Oxide (MOX) fuels, a traditional way to achieve ...

De Roo, Guillaume

2009-01-01T23:59:59.000Z

150

Design and performance of a parachute for the recovery of a 760-lb payload  

SciTech Connect (OSTI)

A 26-ft-diameter ribbon parachute deployed using a pilot parachute system has been developed at Sandia National Laboratories for the recovery of a 760-lb payload released at subsonic and transonic speeds. The wide range of deployment dynamic pressures led to the design, utilizing wind tunnel testing and computer simulation, of a unique pilot parachute system verified in full-scale flight tests. Performance data from 20 full-scale flight tests were used to evaluate system performance and structural validity. The concical ribbon parachute design chosen for this development effort follows the practice of previous Sandia National Laboratory parachute development programs for high performance airdropped payloads. The design process for this parachute system included a tradeoff study to evaluate and compare the performance between an equivalent drag area 26-foot-diameter single parachute system and a cluster system of three 14-ft-diameter parachutes. The results showed a small advantage for the cluster system in inflation and initial deceleration characteristics. However, the higher cost, higher weight, greater packing complexity and greater risk involved in the development of the cluster system outweighed the performance advantages and led to the choice of the 26-ft-diameter parachute as the baseline design for the development. This paper describes the design and performance of the 26-ft-diameter parachute which was chosen for the recovery of a 760-lb payload. The results of 20 full-scale flight test of this parachute system are summarized. 8 refs., 13 figs., 2 tabs.

Waye, D.E.

1991-01-01T23:59:59.000Z

151

Unexpected, Stable Form of Uranium Detected | EMSL  

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

Unexpected, Stable Form of Uranium Detected Unexpected, Stable Form of Uranium Detected Insights on underappreciated reaction could shed light on environmental cleanup options...

152

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

SciTech Connect (OSTI)

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

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

2010-02-01T23:59:59.000Z

153

Conversion of depleted uranium hexafluoride to a solid uranium compound  

DOE Patents [OSTI]

A process for converting UF.sub.6 to a solid uranium compound such as UO.sub.2 and CaF. The UF.sub.6 vapor form is contacted with an aqueous solution of NH.sub.4 OH at a pH greater than 7 to precipitate at least some solid uranium values as a solid leaving an aqueous solution containing NH.sub.4 OH and NH.sub.4 F and remaining uranium values. The solid uranium values are separated from the aqueous solution of NH.sub.4 OH and NH.sub.4 F and remaining uranium values which is then diluted with additional water precipitating more uranium values as a solid leaving trace quantities of uranium in a dilute aqueous solution. The dilute aqueous solution is contacted with an ion-exchange resin to remove substantially all the uranium values from the dilute aqueous solution. The dilute solution being contacted with Ca(OH).sub.2 to precipitate CaF.sub.2 leaving dilute NH.sub.4 OH.

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

2001-01-01T23:59:59.000Z

154

Distribution and a possible mechanism of uranium accumulation in the Catahoula Tuff, Live Oak County, Texas  

E-Print Network [OSTI]

- and micro-scopic distribution of' uranium within the Catahoula Tuff. METHODS A uranium ore body exposed in the Pant Tuff' Member of the Catahoula Tuff and exposed by open-pit mining was inves- tigated in this study. The distribution of the uranium... by oil and mining companies and the United States Geological Survey found numerous radiometric anomalies, In 1959, the San Antonio Mine Company began open pit mining of several small, shallow (less than 15 meters deep) . oxidized ore bodies in Karnes...

Parks, Steven Louis

1979-01-01T23:59:59.000Z

155

2013 Domestic Uranium Production Report  

E-Print Network [OSTI]

Administration (EIA), the statistical and analytical agency within the U.S. Department of Energy. By law, EIA.S. Energy Information Administration | 2013 Domestic Uranium Production Report iii Preface The U.S. Energy://www.eia.doe.gov/glossary/. #12;U.S. Energy Information Administration | 2013 Domestic Uranium Production Report iv Contents

156

Record production on Gary No. 13 blast furnace with 450 lb./THM co-injection rates  

SciTech Connect (OSTI)

Coal injection was initiated on No. 13 Blast Furnace in 1993 with 400 lb/THM achieved in 9 months. In early 1994, cold weather and coal preparation upsets led to the use of a second injectant, oil atomized by natural gas, to supplement the coal. Various combinations of coal and oil were investigated as total injection was increased to 450 lb/THM. Beginning in the last half of 1994, a continuing effort has been made to increase furnace production while maintaining this high co-injection level. Typical furnace production is now in excess of 10,000 THM/day compared with about 8500 THM/day in late 1993.

Schuett, K.J.; White, D.G. [US Steel Group, Gary, IN (United States). Gary Works

1996-12-31T23:59:59.000Z

157

Domestic Uranium Production Report  

Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines AboutDecember 2005 (Thousand9, 2015Year109 AppendixCostsDistributedSep-1410. Uranium

158

Domestic Uranium Production Report  

Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines AboutDecember 2005 (Thousand9, 2015Year109 AppendixCostsDistributedSep-1410. Uranium9.

159

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

160

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium from U.S.2.

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


161

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium from U.S.2.3.

162

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium from U.S.2.3.5.

163

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium from U.S.2.3.5.3.

164

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

165

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

166

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium froma. Uraniumb.7.

167

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

168

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelines About U.S. NaturalA. Michael SchaalNovember1. Foreign sales of uranium froma.9.

169

Fingerprinting Uranium | EMSL  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsing ZirconiaPolicyFeasibilityField Office FinalFinancingFingerprinting Uranium

170

Electronic structure and ionicity of actinide oxides from first principles L. Petit,1,2,* A. Svane,1 Z. Szotek,2 W. M. Temmerman,2 and G. M. Stocks3  

E-Print Network [OSTI]

. A mixture of UO2 and PuO2, where Pu is blended with either natural or depleted uranium, constitutes. INTRODUCTION Actinide oxides play a dominant role in the nuclear fuel cycle.1 For many years, uranium dioxide

Svane, Axel Torstein

171

National uranium resource evaluation. Geology and recognition criteria for sandstone uranium deposits of the salt wash type, Colorado Plateau Province. Final report  

SciTech Connect (OSTI)

The uranium-vanadium deposits of the Salt Wash Member of the Morrison Formation in the Colorado Plateau are similar to sandstone uranium deposits elsewhere in the USA. The differences between Salt Wash deposits and other sandstone uranium deposits are also significant. The Salt Wash deposits are unique among sandstone deposits in that they are dominantly vanadium deposits with accessory uranium. The Salt Wash ores generally occur entirely within reduced sandstone, without adjacent tongues of oxidized sandstone. They are more like the deposits of Grants, which similarly occur in reduced sandstones. Recent studies of the Grants deposits have identified alteration assemblages which are asymmetrically distributed about the deposits and provide a basis for a genetic model for those deposits. The alteration types recognized by Shawe in the Slick Rock district may provide similar constraints on ore formation when expanded to broader areas and more complete chemical analyses.

Thamm, J.K.; Kovschak, A.A. Jr.; Adams, S.S.

1981-01-01T23:59:59.000Z

172

Corrosion of Aluminum-Uranium Alloys in Water Vapor at 200\\260C  

SciTech Connect (OSTI)

Coupons of aluminum-uranium alloys at 10 and 18 weight percent were exposed to a saturated water vapor condition at 200 degrees C up to about 1500 hours and compared to previous results for aluminum 1100. The aluminum-uranium materials exhibited a range of initial corrosion rates and approached similar rates with the formation of a passive film of boehmite (Al2O3oH2O). The cast and extruded 10 percent uranium, having a primary aluminum-eutectic microstructure, was more corrosion resistant than the 18% cast and extruded. The initial corrosion rates of the aluminum-uranium materials were one to four times higher than that for aluminum 1100. It is postulated that a micro-galvanic coupling between the large UAl4 particles and the aluminum matrix has caused the variation. Sectioning the exposed specimens shows different characteristics of the oxide layers. In the case of the cast and extruded Al-10 percent U alloy, small uranium aluminide particles can be seen in the boehmite matrix and do not seem to be corroded. The oxide film of the Al-18 percent U alloy appears to have two distinct oxide layers. The outer layer has mass aggregates formed in the aluminum oxide matrix, while the inner layer contains UAl4 particles as in the case of Al-10 percent U

Lam, P.S.

1998-11-25T23:59:59.000Z

173

Contents of environmental impact statements prepared for the Uranium Mill Tailings Remedial Action Project. [Uranium Mill Tailings Remedial Action (UMTRA) Project  

SciTech Connect (OSTI)

This document presents two versions of the outline for the environmental impact statements (EISS) to be prepared for the Uranium Mill Tailings Remedial Action (UMTRA) Project. The first displays the basic structure of the statements; it lists only the titles of sections. The second is a guide to the contents of the statements which provides, under each title, a brief summary of contents. The outline is intended to comply with the planning requirements and the definitions of terms established by the Council on Environmental Quality as well as DOE Order 5440.lB (Implementation of the National Environmental Policy Act), and compliance with Floodplain/Wetlands Environmental Review Requirements. These requirements and definitions are implicity part of the outline. The outline presented in this document will guide the preparation of EISs Guidelines for preparation of environmental assessments for the UMTRA Project are available.

Not Available

1986-01-01T23:59:59.000Z

174

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

175

Microwell Plate Luminometer -LB 96V MicrolumatPlus luminomet... http://www.berthold.com.au/bioanalytical_pages/LB96V.html 1 of 3 3/19/06 1:31 PM  

E-Print Network [OSTI]

://www.berthold.com.au/bioanalytical_pages/LB96V.html 1 of 3 3/19/06 1:31 PM | Home | Industrial Measurement | Radiation Protection | Life for all applications in luminescence measurement. For overload detection, the optical channel is shutterGlow software offers the possibility to control the instrument with a Windows based system. Robot access

Raizada, Manish N.

176

The End of Cheap Uranium  

E-Print Network [OSTI]

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.

Michael Dittmar

2011-06-21T23:59:59.000Z

177

Innovative Approach to Prevent Acid Drainage from Uranium Mill Tailings Based on the Application of Na-Ferrate (VI)  

SciTech Connect (OSTI)

The operation of uranium mining and milling plants gives rise to huge amounts of wastes from both mining and milling operations. When pyrite is present in these materials, the generation of acid drainage can take place and result in the contamination of underground and surface waters through the leaching of heavy metals and radionuclides. To solve this problem, many studies have been conducted to find cost-effective solutions to manage acid mine drainage; however, no adequate strategy to deal with sulfide-ric h wastes is currently available. Ferrate (VI) is a powerful oxidizing agent in aqueous media. Under acidic conditions, the redox potential of the Ferrate (VI) ion is the highest of any other oxidant used in wastewater treatment processes. The standard half cell reduction potential of ferrate (VI) has been determined as +2.20 V to + 0.72 V in acidic and basic solutions, respectively. Ferrate (VI) exhibits a multitude of advantageous properties, including higher reactivity and selectivity than traditional oxidant alternatives, as well as disinfectant, flocculating, and coagulant properties. Despite numerous beneficial properties in environmental applications, ferrate (VI) has remained commercially unavailable. Starting in 1953, different methods for producing a high purity, powdered ferrate (VI) product were developed. However, producing this dry, stabilized ferrate (VI) product required numerous process steps which led to excessive synthesis costs (over $20/lb) thereby preventing bulk industrial use. Recently a novel synthesis method for the production of a liquid ferrate (VI) based on hypochlorite oxidation of ferric ion in strongly alkaline solutions has been discovered (USPTO 6,790,428; September 14, 2004). This on-site synthesis process dramatically reduces manufacturing cost for the production of ferrate (VI) by utilizing common commodity feedstocks. This breakthrough means that for the first time ferrate (VI) can be an economical alternative to treating acid mining drainage generating materials. The objective of the present study was to investigate a methodology of preventing the generation of acid drainage by applying ferrate (VI) to acid generating materials prior to the disposal in impoundments or piles. Oxidizing the pyritic material in mining waste could diminish the potential for acid generation and its related environmental risks and long-term costs at disposal sites. The effectiveness of toxic metals removal from acid mine drainage by applying ferrate (VI) is also examined. Preliminary results presented in this paper show that the oxidation of pyrite by ferrate is a first-order rate reaction in Fe(VI) with a half-life of about six hours. The stability of Fe(VI) in water solutions will not influence the reaction rate in a significant manner. New low-cost production methods for making liquid ferrate on-site makes this technology a very attractive option to mitigate one of the most pressing environmental problems in the mining industry. (authors)

Fernandes, H.M.; Reinhart, D.; Lettie, L.; Franklin, M.R. [University of Central Florida, P.O. Box. 162450, Orlando, FL, 32816-2450 (United States); Fernandes, H.M.; Franklin, M.R. [Institute of Radiation Protection and Dosimetry (IRD), Av. Salvador Allende s/n - Recreio - Rio de Janeiro - RJ - 22795-090 (Brazil); Sharma, V. [Florida Institute of Technology, 150 West University Boulevard, Melbourne, FL 32901 (United States); Daly, L.J. [Ferrate Treatment Technologies, LLC, 6432 Pine Castle Blvd. Unit 2C, Orlando, FL, 32809 (United States)

2006-07-01T23:59:59.000Z

178

Investigations of factors affecting the use of uranium metal as a source of alpha particles for the evaluation of alpha track detectors  

E-Print Network [OSTI]

, an uranium foil was used as the alpha particle source. The foil created new problems which needed to be studied in detail. Among these problems, the effect of the thickness of the oxide layer on the uranium metal foil surface was the most important. To study...

Voirin, Marc

1994-01-01T23:59:59.000Z

179

Evidence for Alkane Coordination to an Electron-Rich Uranium Center Ingrid Castro-Rodriguez, Hidetaka Nakai, Peter Gantzel, Lev N. Zakharov, Arnold L. Rheingold, and  

E-Print Network [OSTI]

Evidence for Alkane Coordination to an Electron-Rich Uranium Center Ingrid Castro of Chemistry and Biochemistry, UniVersity of California, San Diego, 9500 Gilman DriVe, MC 0358, La Jolla adducts of the low-valent, coordinatively unsaturated, tris-aryl oxide uranium(III) complex [((ArO)3tacn

Meyer, Karsten

180

Safe Operating Procedure SAFETY PROTOCOL: URANIUM  

E-Print Network [OSTI]

involve the use of natural or depleted uranium. Natural isotopes of uranium are U-238, U-235 and U-234 (see Table 1 for natural abundances). Depleted uranium contains less of the isotopes: U-235 and U-234. The specific activity of depleted uranium (5.0E-7 Ci/g) is less than that of natural uranium (7.1E-7 Ci

Farritor, Shane

Note: This page contains sample records for the topic "uranium oxide lb" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
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We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


181

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

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

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

182

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

SciTech Connect (OSTI)

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

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

2003-10-01T23:59:59.000Z

183

Process for the recovery of uranium from wet-process phosphoric acid  

SciTech Connect (OSTI)

In a process for the recovery of uranium from a wet-process phosphoric acid, comprising treating in an extraction step the preliminarily oxidized acid first with an organic solvent consisting essentially of a dialkylphosphoric acid and a trialkyphosphine oxide dissolved in an inert and unreactive organic solvent whereby there are obtained a uranium-free phosphoric acid and an organic extract consisting essentially of the solvent containing the major portion of uranium; then, in a reextraction step, separating the uranium from the organic extract as ammonium uranyl tricarbonate by reacting the organic extract with ammonium hydroxide and ammonium carbonate; and recycling the uranium-free solvent to the extraction step; an improvement comprises treating the organic extract in a reextraction apparatus having at least two stages, by (A) introducing the extract at the head of the first stage; (B) countercurrently introducing ammonia or ammonium hydroxide solution at the bottom of the first stage; the ph of the first stage being controlled and maintained at a value of 8.0 to 8.5; (C) introducing an ammonium carbonate aqueous solution at the bottom of the last stage; the amount of ammonium carbonate employed being 50-80 percent by weight of the theoretical molar quantity which is necessary to neutralize the dialkylphosphoric acid contained in the solvent and to convert the uranium to ammonium uranyl tricarbonate; and (D) regenerating the ammoniated solvent obtained after the reextraction step by treating it with an acid before recycling it to the extraction step.

Francois, A.; Sialino, A.

1980-12-09T23:59:59.000Z

184

Laser induced phosphorescence uranium analysis  

DOE Patents [OSTI]

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.

Bushaw, Bruce A. (Kennewick, WA)

1986-01-01T23:59:59.000Z

185

Laser induced phosphorescence uranium analysis  

DOE Patents [OSTI]

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.

Bushaw, B.A.

1983-06-10T23:59:59.000Z

186

Neutron-Rich Isotope Production Using a Uranium Carbide Carbon Nanotubes SPES Target Prototype  

SciTech Connect (OSTI)

The SPES (Selective Production of Exotic Species) project, under development at the Istituto Nazionale di Fisica Nucleare - Laboratori Nazionali di Legnaro (INFN-LNL), is a new-generation Isotope Separation On-Line (ISOL) facility for the production of radioactive ion beams by means of the proton-induced fission of uranium. In the framework of the research on the SPES target, seven uranium carbide discs, obtained by reacting uranium oxide with graphite and carbon nanotubes, were irradiated with protons at the Holifield Radioactive Ion Beam Facility (HRIBF) of Oak Ridge National Laboratory (ORNL). In the following, the yields of several fission products obtained during the experiment are presented and discussed. The experimental results are then compared to those obtained using a standard uranium carbide target. The reported data highlights the capability of the new type of SPES target to produce and release isotopes of interest for the nuclear physics community.

Corradetti, Stefano [ORNL; Biasetto, Lisa [INFN, Laboratori Nazionali di Legnaro, Italy; Manzolaro, Mattia [INFN, Laboratori Nazionali di Legnaro, Italy; Scarpa, Daniele [ORNL; Carturan, S. [INFN, Laboratori Nazionali di Legnaro, Italy; Andrighetto, Alberto [INFN, Laboratori Nazionali di Legnaro, Italy; Prete, Gianfranco [ORNL; Vasquez, Jose L [ORNL; Zanonato, P. [Dipartimento di Scienze Chimiche, Padova, Italy; Colombo, P. [Dipartimento di Ingegneria Meccanica, Padova, Italy; Jost, Carola [University of Tennessee, Knoxville (UTK); Stracener, Daniel W [ORNL

2013-01-01T23:59:59.000Z

187

Potential incorporation of transuranics into uranium phases  

SciTech Connect (OSTI)

The UO{sub 2} in spent nuclear fuel is unstable under moist oxidizing conditions and will be altered to uranyl oxide hydrate phases. The transuranics released during the corrosion of spent fuel may also be incorporated into the structures of secondary U{sup 6+} phases. The incorporation of radionuclides into alteration products will affect their mobility. A series of precipitation tests were conducted at either 150 or 90 C for seven days to determine the potential incorporation of Ce{sup 4+} and Nd{sup 3+} (surrogates for Pu{sup 4+} and Am{sup 3+}, respectively) into uranium phases. Ianthinite ([U{sub 2}{sup 4+}(UO{sub 2}){sub 4}O{sub 6}(OH){sub 4}(H{sub 2}O){sub 4}](H{sub 2}O){sub 5}) was produced by dissolving uranium oxyacetate in a solution containing copper acetate monohydrate as a reductant. The leachant used in these tests were doped with either 2.1 ppm cerium or 399 ppm neodymium. Inductively coupled plasma-mass spectrometer (ICP-MS) analysis of the solid phase reaction products which were dissolved in a HNO{sub 3} solution indicates that about 306 ppm Ce (K{sub d} = 146) was incorporated into ianthinite, while neodymium contents were much higher, being approximately 24,800 ppm (K{sub d} = 62). Solid phase examinations using an analytical transmission electron microscope/electron energy-loss spectrometer (AEM/EELS) indicate a uniform distribution of Nd, while Ce contents were below detection. Becquerelite (Ca[(UO{sub 2}){sub 6}O{sub 4}(OH){sub 6}]{center_dot}8H{sub 2}O) was produced by dissolving uranium oxyacetate in a solution containing calcium acetate. The leachant in these tests was doped with either 2.1 ppm cerium or 277 ppm neodymium. ICP-MS results indicate that about 33 ppm Ce (K{sub d}=16) was incorporated into becquerelite, while neodymium contents were higher, being approximately 1,300 ppm (K{sub d}=5). Homogeneous distribution of Nd in the solid phase was noted during AEM/EELS examination, and Ce contents were also below detection.

Kim, C. W.; Wronkiewicz, D. J.; Buck, E. C.

1999-12-07T23:59:59.000Z

188

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]

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

American Society for Testing and Materials. Philadelphia

2007-01-01T23:59:59.000Z

189

Contents of environmental impact statements prepared for the Uranium Mill Tailings Remedial Action Project  

SciTech Connect (OSTI)

This document presents two versions of the outline for the environmental impact statements (EISS) to be prepared for the Uranium Mill Tailings Remedial Action (UMTRA) Project. The first displays the basic structure of the statements; it lists only the titles of sections. The second is a guide to the contents of the statements which provides, under each title, a brief summary of contents. The outline is intended to comply with the planning requirements and the definitions of terms established by the Council on Environmental Quality as well as DOE Order 5440.lB (Implementation of the National Environmental Policy Act), and compliance with Floodplain/Wetlands Environmental Review Requirements. These requirements and definitions are implicity part of the outline. The outline presented in this document will guide the preparation of EISs Guidelines for preparation of environmental assessments for the UMTRA Project are available.

Not Available

1986-01-01T23:59:59.000Z

190

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

SciTech Connect (OSTI)

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

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

2011-02-01T23:59:59.000Z

191

Uranium chloride extraction of transuranium elements from LWR fuel  

DOE Patents [OSTI]

A process of separating transuranium actinide values from uranium values present in spent nuclear oxide fuels containing rare earth and noble metal fission products as well as other fission products is disclosed. The oxide fuel is reduced with Ca metal in the presence of Ca chloride and a U-Fe alloy which is liquid at about 800 C to dissolve uranium metal and the noble metal fission product metals and transuranium actinide metals and rare earth fission product metals leaving Ca chloride having CaO and fission products of alkali metals and the alkali earth metals and iodine dissolved therein. The Ca chloride and CaO and the fission products contained therein are separated from the U-Fe alloy and the metal values dissolved therein. The U-Fe alloy having dissolved therein reduced metals from the spent nuclear fuel is contacted with a mixture of one or more alkali metal or alkaline earth metal halides selected from the class consisting of alkali metal or alkaline earth metal and Fe or U halide or a combination thereof to transfer transuranium actinide metals and rare earth metals to the halide salt leaving the uranium and some noble metal fission products in the U-Fe alloy and thereafter separating the halide salt and the transuranium metals dissolved therein from the U-Fe alloy and the metals dissolved therein. 1 figure.

Miller, W.E.; Ackerman, J.P.; Battles, J.E.; Johnson, T.R.; Pierce, R.D.

1992-08-25T23:59:59.000Z

192

Uranium chloride extraction of transuranium elements from LWR fuel  

DOE Patents [OSTI]

A process of separating transuranium actinide values from uranium values present in spent nuclear oxide fuels containing rare earth and noble metal fission products as well as other fission products is disclosed. The oxide fuel is reduced with Ca metal in the presence of Ca chloride and a U-Fe alloy which is liquid at about 800.degree. C. to dissolve uranium metal and the noble metal fission product metals and transuranium actinide metals and rare earth fission product metals leaving Ca chloride having CaO and fission products of alkali metals and the alkali earth metals and iodine dissolved therein. The Ca chloride and CaO and the fission products contained therein are separated from the U-Fe alloy and the metal values dissolved therein. The U-Fe alloy having dissolved therein reduced metals from the spent nuclear fuel is contacted with a mixture of one or more alkali metal or alkaline earth metal halides selected from the class consisting of alkali metal or alkaline earth metal and Fe or U halide or a combination thereof to transfer transuranium actinide metals and rare earth metals to the halide salt leaving the uranium and some noble metal fission products in the U-Fe alloy and thereafter separating the halide salt and the transuranium metals dissolved therein from the U-Fe alloy and the metals dissolved therein.

Miller, William E. (Naperville, IL); Ackerman, John P. (Downers Grove, IL); Battles, James E. (Oak Forest, IL); Johnson, Terry R. (Wheaton, IL); Pierce, R. Dean (Naperville, IL)

1992-01-01T23:59:59.000Z

193

Characterization of Alpha-Phase Sintering of Uranium and Uranium-Zirconium Alloys for Advanced Nuclear Fuel Applications  

E-Print Network [OSTI]

The sintering behavior of uranium and uranium-zirconium alloys in the alpha phase were characterized in this research. Metal uranium powder was produced from pieces of depleted uranium metal acquired from the Y-12 plant via hydriding...

Helmreich, Grant

2012-02-14T23:59:59.000Z

194

Evidence of uranium biomineralization in sandstone-hosted roll-front uranium deposits, northwestern China  

E-Print Network [OSTI]

Evidence of uranium biomineralization in sandstone-hosted roll-front uranium deposits, northwestern Available online 25 January 2005 Abstract We show evidence that the primary uranium minerals, uraninite-front uranium deposits, Xinjiang, northwestern China were biogenically precipitated and psuedomorphically

Fayek, Mostafa

195

Uranium Acquisition | Y-12 National Security Complex  

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

of Interest (EOI) to acquire up to 6,800 metric tons of Uranium (MTU) of high purity depleted uranium metal (DU) and related material and services. This request for EOI does...

196

The End of Cheap Uranium  

E-Print Network [OSTI]

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...

Dittmar, Michael

2011-01-01T23:59:59.000Z

197

In Situ Community Control of the Stability of Bioreduced Uranium  

SciTech Connect (OSTI)

The overall objective of this research is to understand the mechanisms for maintenance of bio-reduced uranium in an aerobic to microaerophylic aquifer under actual field conditions after electron donor addition for biostimulation has ended. Primary Objectives: (1) Determine the relative importance of microbial communities and/or chemical and physical environments mediating uranium reduction/oxidation after cessation of donor addition in an aerobic aquifer. (2) Determine, after cessation of donor addition, the linkages between microbial functions and abiotic processes mediating. Initial Hypotheses: (1) The typical bio-reduced subsurface environments that maintain U(VI) reduction rates after biostimulation contain limited amounts of oxidized iron on mineral surfaces. Therefore, the non sulfate-reducing dissimilatory iron reducing bacteria will move to more conducive areas or be out-competed by more versatile microbes. (2) Microbes capable of sulfate reduction play an important role in the post-treatment maintenance of bio-reduced uranium because these bacteria either directly reduce U(VI) or generate H2S, and/or FeS0.9 which act as oxygen sinks maintaining U(IV) in a reduced state. (3) The presence of bioprecipitated amorphous FeS0.9 in sediments will maintain low U(IV) reoxidation rates under conditions of low biomass, but FeS0.9 by itself is not sufficient to remove U(VI) from groundwater by abiotic reduction. FIELD SCALE EXPERIMENTS: Field-scale electron donor amendment experiments were conducted in 2002, 2003, and 2004 at the Old Rifle Uranium Mill Tailings Remedial Action (UMTRA) site in Rifle, Colorado.

White, David C.

2006-06-01T23:59:59.000Z

198

230Th-234U Age-Dating Uranium by Mass Spectrometry  

SciTech Connect (OSTI)

This is the standard operating procedure used by the Isotope Ratio Mass Spectrometry Group of the Chemical Sciences Division at LLNL for the preparation of a sample of uranium oxide or uranium metal for {sup 230}Th-{sup 234}U age-dating. The method described here includes the dissolution of a sample of uranium oxide or uranium metal, preparation of a secondary dilution, spiking of separate aliquots for uranium and thorium isotope dilution measurements, and purification of uranium and thorium aliquots for mass spectrometry. This SOP may be applied to uranium samples of unknown purity as in a nuclear forensic investigation, and also to well-characterized samples such as, for example, U{sub 3}O{sub 8} and U-metal certified reference materials. The sample of uranium is transferred to a quartz or PFA vial, concentrated nitric acid is added and the sample is heated on a hotplate at approximately 100 C for several hours until it dissolves. The sample solution is diluted with water to make the solution approximately 4 M HNO{sub 3} and hydrofluoric acid is added to make it 0.05 M HF. A secondary dilution of the primary uranium solution is prepared. Separate aliquots for uranium and thorium isotope dilution measurements are taken and spiked with {sup 233}U and {sup 229}Th, respectively. The spiked aliquot for uranium isotope dilution analysis is purified using EiChrom UTEVA resin. The spiked aliquot for thorium isotope dilution analysis is purified by, first, a 1.8 mL AG1x8 resin bed in 9 M HCl on which U adsorbs and Th passes through; second, adsorbing Th on a 1 mL AG1x8 resin bed in 8 M HNO{sub 3} and then eluting it with 9 M HCl followed by 0.1 M HCl + 0.005 M HF; and third, by passing the Th through a final 1.0 mL AG1x8 resin bed in 9 M HCl. The mass spectrometry is performed using the procedure 'Th and U Mass Spectrometry for {sup 230}Th-{sup 234}U Age Dating'.

Williams, R W; Gaffney, A M

2012-04-18T23:59:59.000Z

199

Multicomponent reactive transport modeling of uranium bioremediation field experiments  

SciTech Connect (OSTI)

Biostimulation field experiments with acetate amendment are being performed at a former uranium mill tailings site in Rifle, Colorado, to investigate subsurface processes controlling in situ bioremediation of uranium-contaminated groundwater. An important part of the research is identifying and quantifying field-scale models of the principal terminal electron-accepting processes (TEAPs) during biostimulation and the consequent biogeochemical impacts to the subsurface receiving environment. Integrating abiotic chemistry with the microbially mediated TEAPs in the reaction network brings into play geochemical observations (e.g., pH, alkalinity, redox potential, major ions, and secondary minerals) that the reactive transport model must recognize. These additional constraints provide for a more systematic and mechanistic interpretation of the field behaviors during biostimulation. The reaction network specification developed for the 2002 biostimulation field experiment was successfully applied without additional calibration to the 2003 and 2007 field experiments. The robustness of the model specification is significant in that 1) the 2003 biostimulation field experiment was performed with 3 times higher acetate concentrations than the previous biostimulation in the same field plot (i.e., the 2002 experiment), and 2) the 2007 field experiment was performed in a new unperturbed plot on the same site. The biogeochemical reactive transport simulations accounted for four TEAPs, two distinct functional microbial populations, two pools of bioavailable Fe(III) minerals (iron oxides and phyllosilicate iron), uranium aqueous and surface complexation, mineral precipitation, and dissolution. The conceptual model for bioavailable iron reflects recent laboratory studies with sediments from the Old Rifle Uranium Mill Tailings Remedial Action (UMTRA) site that demonstrated that the bulk (~90%) of Fe(III) bioreduction is associated with the phyllosilicates rather than the iron oxides. The uranium reaction network includes a U(VI) surface complexation model based on laboratory studies with Old Rifle UMTRA sediments and aqueous complexation reactions that include ternary complexes (e.g., calcium-uranyl-carbonate). The bioreduced U(IV), Fe(II), and sulfide components produced during the experiments are strongly associated with the solid phases and may play an important role in long-term uranium immobilization.

Fang, Yilin; Yabusaki, Steven B.; Morrison, Stan J.; Amonette, James E.; Long, Philip E.

2009-10-15T23:59:59.000Z

200

Greater solubility usually = greater toxicity Chromium (Cr) Six oxidation states, +1, +2, +3, +4, +5, +6  

E-Print Network [OSTI]

(depleted uranium) · 4 oxidation states (+4, +6 most common) · U(VI) water-soluble, U(IV) in-soluble Metals Uranium ­ heaviest natural element - 17 isotopes · Natural form % = U-238 (99.27), U-235 (0.72), U-234 (0 in nuclear fuel ­ U-235 (readily fissionable) · Used in nuclear and conventional weapons · Uranium enrichment

Bruns, Tom

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


201

Assessment of the Group 5-6 (LB C2, LB S2, LV S1) Stack Sampling Probe Locations for Compliance with ANSI/HPS N13.1 1999  

SciTech Connect (OSTI)

This document reports on a series of tests to assess the proposed air sampling locations for the Hanford Tank Waste Treatment and Immobilization Plant (WTP) Group 5-6 exhaust stacks with respect to the applicable criteria regarding the placement of an air sampling probe. The LB-C2, LV-S1, and LB S2 exhaust stacks were tested together as a group (Test Group 5-6) because the common factor in their design is that the last significant flow disturbance upstream of the air sampling probe is a reduction in duct diameter. Federal regulations( ) require that a sampling probe be located in the exhaust stack according to the criteria of the American National Standards Institute/Health Physics Society (ANSI/HPS) N13.1-1999, Sampling and Monitoring Releases of Airborne Radioactive Substances from the Stack and Ducts of Nuclear Facilities. These criteria address the capability of the sampling probe to extract a sample that represents the effluent stream. The testing on scale models of the stacks conducted for this project was part of the River Protection Project—Waste Treatment Plant Support Program under Contract No. DE-AC05-76RL01830 according to the statement of work issued by Bechtel National Inc. (BNI, 24590-QL-SRA-W000-00101, N13.1-1999 Stack Monitor Scale Model Testing and Qualification, Revision 1, 9/12/2007) and Work Authorization 09 of Memorandum of Agreement 24590-QL-HC9-WA49-00001. The internal Pacific Northwest National Laboratory (PNNL) project for this task is 53024, Work for Hanford Contractors Stack Monitoring. The testing described in this document was further guided by the Test Plan Scale Model Testing the Waste Treatment Plant LB-C2, LB-S2, and LV-S1 (Test Group 5-6) Stack Air Sampling Positions (TP-RPP-WTP-594). The tests conducted by PNNL during 2009 and 2010 on the Group 5-6 scale model systems are described in this report. The series of tests consists of various measurements taken over a grid of points in the duct cross-section at the designed sampling probe locations and at five duct diameters up and downstream from the design location to accommodate potential construction variability. The tests were done only at the design sampling probe location on the scale model of LB-S2 because that ductwork was already constructed. The ANSI/HPS N13.1-1999 criteria and the corresponding results of the test series on the scale models are summarized in this report.

Glissmeyer, John A.; Flaherty, Julia E.; Piepel, Gregory F.

2011-03-11T23:59:59.000Z

202

Uranium-233 purification and conversion to stabilized ceramic grade urania for LWBR fuel fabrication (LWBR Development Program)  

SciTech Connect (OSTI)

High purity ceramic grade urania (/sup 233/UO/sub 2/) used in manufacturing the fuel for the Light Water Breeder Reactor (LWBR) core was made from uranium-233 that was obtained by irradiating thoria under special conditions to result in not more than 10 ppM of uranium-232 in the recovered uranium-233 product. A developmental study established the operating parameters of the conversion process for transforming the uranium-233 into urania powder with the appropriate chemical and physical attributes for use in fabricating the LWBR core fuel. This developmental study included the following: (a) design of an ion exchange purification process for removing the gamma-emitting alpha-decay daughters of uranium-232, to reduce the gamma-radiation field of the uranium-233 during LWBR fuel manufacture; (b) definition of the parameters for precipitating the uranium-233 as ammonium uranate (ADU) and for reducing the ADU with hydrogen to yield a urania conversion product of the proper particle size, surface area and sinterability for use in manufacturing the LWBR fuel; (c) establishment of parameters and design of equipment for stabilizing the urania conversion product to prevent it from undergoing excessive oxidation on exposure to the air during LWBR fuel manufacturing operations; and (d) development of a procedure and a facility to reprocess the unirradiated thoria-urania fuel scrap from the LWBR core manufacturing operations to recover the uranium-233 and convert it into high purity ceramic grade urania for LWBR core fabrication.

Lloyd, R.

1980-10-01T23:59:59.000Z

203

High strength uranium-tungsten alloys  

DOE Patents [OSTI]

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.

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)

1991-01-01T23:59:59.000Z

204

High strength uranium-tungsten alloy process  

DOE Patents [OSTI]

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.

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)

1990-01-01T23:59:59.000Z

205

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 operating uranium mill tailings (Subpart W) Status update on Subpart W activities Outreach/Communications #12;3 EPA Regulatory Requirements for Operating Uranium Mill Tailings (Clean Air Act) · 40 CFR 61

206

URANIUM MILL TAILINGS RADON FLUX CALCULATIONS  

E-Print Network [OSTI]

URANIUM MILL TAILINGS RADON FLUX CALCULATIONS PIĂ?ON RIDGE PROJECT MONTROSE COUNTY, COLORADO Inc. (Golder) was commissioned by EFRC to evaluate the operations of the uranium mill tailings storage in this report were conducted using the WISE Uranium Mill Tailings Radon Flux Calculator, as updated on November

207

Remediation and Recovery of Uranium from Contaminated  

E-Print Network [OSTI]

Remediation and Recovery of Uranium from Contaminated Subsurface Environments with Electrodes K E L that Geobacter species can effectively remove uranium from contaminated groundwater by reducing soluble U was stably precipitated until reoxidized in the presence of oxygen. When an electrode was placed in uranium

Lovley, Derek

208

Uranium Watch REGULATORY CONFUSION: FEDERALAND STATE  

E-Print Network [OSTI]

Uranium Watch Report REGULATORY CONFUSION: FEDERALAND STATE ENFORCEMENT OF 40 C.F.R. PART 61 SUBPART W INTRODUCTION 1. This Uranium Watch Report, Regulatory Confusion: Federal and State Enforcement at the White Mesa Uranium Mill, San Juan County, Utah. 2. The DAQ, a Division of the Utah Department

209

D Riso-R-429 Automated Uranium  

E-Print Network [OSTI]

routinely used analytical techniques for uranium determina- tions in geological samples, fissionCM i D Riso-R-429 Automated Uranium Analysis by Delayed-Neutron Counting H. Kunzendorf, L. Løvborg AUTOMATED URANIUM ANALYSIS BY DELAYED-NEUTRON COUNTING H. Kunzendorf, L. Løvborg and E.M. Christiansen

210

Y-12 Uranium Exposure Study  

SciTech Connect (OSTI)

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

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

1999-08-05T23:59:59.000Z

211

Modeling of UO{sub 2} oxidation in steam atmosphere  

SciTech Connect (OSTI)

Nuclear fuel oxidation is an important phenomenon affecting fission product behavior. As indicated by a number of studies, uranium dioxide shows a very wide range of nonstoichiometric states. In steam, fuel oxidation produces a hyperstoichiometric composition, changing the transport properties. Variation of stoichiometry changes diffusion coefficients for oxygen, noble gases, and fission products substantially, affecting the release of fission products.

Dobrov, B.V.; Likhanskii, V.V. [Triniti Research Center, Triniti, Moscow (Russian Federation); Ozrin, V.D. [Nuclear Safety Institute IBREA, Moscow (Russian Federation)] [and others

1997-12-01T23:59:59.000Z

212

Aquifer restoration at in-situ leach uranium mines: evidence for natural restoration processes  

SciTech Connect (OSTI)

Pacific Northwest Laboratory conducted experiments with aquifer sediments and leaching solution (lixiviant) from an in-situ leach uranium mine. The data from these laboratory experiments and information on the normal distribution of elements associated with roll-front uranium deposits provide evidence that natural processes can enhance restoration of aquifers affected by leach mining. Our experiments show that the concentration of uranium (U) in solution can decrease at least an order of magnitude (from 50 to less than 5 ppM U) due to reactions between the lixiviant and sediment, and that a uranium solid, possibly amorphous uranium dioxide, (UO/sub 2/), can limit the concentration of uranium in a solution in contact with reduced sediment. The concentrations of As, Se, and Mo in an oxidizing lixiviant should also decrease as a result of redox and precipitation reactions between the solution and sediment. The lixiviant concentrations of major anions (chloride and sulfate) other than carbonate were not affected by short-term (less than one week) contact with the aquifer sediments. This is also true of the total dissolved solids level of the solution. Consequently, we recommend that these solution parameters be used as indicators of an excursion of leaching solution from the leach field. Our experiments have shown that natural aquifer processes can affect the solution concentration of certain constituents. This effect should be considered when guidelines for aquifer restoration are established.

Deutsch, W.J.; Serne, R.J.; Bell, N.E.; Martin, W.J.

1983-04-01T23:59:59.000Z

213

Process for alloying uranium and niobium  

DOE Patents [OSTI]

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.

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

1991-01-01T23:59:59.000Z

214

Composite catalyst for carbon monoxide and hydrocarbon oxidation  

DOE Patents [OSTI]

A method and composition for the complete oxidation of carbon monoxide and/or hydrocarbon compounds. The method involves reacting the carbon monoxide and/or hydrocarbons with an oxidizing agent in the presence of a metal oxide composite catalyst. The catalyst is prepared by combining fluorite-type oxygen ion conductors with active transition metals. The fluorite oxide, selected from the group consisting of cerium oxide, zirconium oxide, thorium oxide, hafnium oxide, and uranium oxide, and may be doped by alkaline earth and rare earth oxides. The transition metals, selected from the group consisting of molybdnum, copper, cobalt, maganese, nickel, and silver, are used as additives. The atomic ratio of transition metal to fluorite oxide is less than one.

Liu, Wei (Cambridge, MA); Flytzani-Stephanopoulos, Maria (Winchester, MA)

1996-01-01T23:59:59.000Z

215

Composite catalyst for carbon monoxide and hydrocarbon oxidation  

DOE Patents [OSTI]

A method and composition are disclosed for the complete oxidation of carbon monoxide and/or hydrocarbon compounds. The method involves reacting the carbon monoxide and/or hydrocarbons with an oxidizing agent in the presence of a metal oxide composite catalyst. The catalyst is prepared by combining fluorite-type oxygen ion conductors with active transition metals. The fluorite oxide, selected from the group consisting of cerium oxide, zirconium oxide, thorium oxide, hafnium oxide, and uranium oxide, and may be doped by alkaline earth and rare earth oxides. The transition metals, selected from the group consisting of molybdenum, copper, cobalt, manganese, nickel, and silver, are used as additives. The atomic ratio of transition metal to fluorite oxide is less than one.

Liu, W.; Flytzani-Stephanopoulos, M.

1996-03-19T23:59:59.000Z

216

Radiochemistry of uranium, neptunium and plutonium: an updating  

SciTech Connect (OSTI)

This report presents some procedures used in the radiochemical isolation, purification and/or analysis of uranium, neptunium, and plutonium. In this update of the procedures, we have not attempted to discuss the developments in the chemistry of U, Np, and Pu but have restricted the report to the newer procedures, most of which have resulted from the increased emphasis in environmental concern which requires analysis of extremely small amounts of the actinide element in quite complex matrices. The final section of this report describes several schemes for isolation of actinides by oxidation state.

Roberts, R.A.; Choppin, G.R.; Wild, J.F.

1986-02-01T23:59:59.000Z

217

Uranium 2014 resources, production and demand  

E-Print Network [OSTI]

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. It presents the results of a thorough review of world uranium supplies and demand 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. Long-term projections of nuclear generating capacity and reactor-related uranium requirements 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 changes in the industry.

Organisation for Economic Cooperation and Development. Paris

2014-01-01T23:59:59.000Z

218

Uranium 2005 resources, production and demand  

E-Print Network [OSTI]

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...

Organisation for Economic Cooperation and Development. Paris

2006-01-01T23:59:59.000Z

219

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

SciTech Connect (OSTI)

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

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

1987-01-01T23:59:59.000Z

220

Standard test method for analysis of isotopic composition of uranium in nuclear-grade fuel material by quadrupole inductively coupled plasma-mass spectrometry  

E-Print Network [OSTI]

1.1 This test method is applicable to the determination of the isotopic composition of uranium (U) in nuclear-grade fuel material. The following isotopic weight percentages are determined using a quadrupole inductively coupled plasma-mass spectrometer (Q-ICP-MS): 233U, 234U, 235U, 236U, and 238U. The analysis can be performed on various material matrices after acid dissolution and sample dilution into water or dilute nitric (HNO3) acid. These materials include: fuel product, uranium oxide, uranium oxide alloys, uranyl nitrate (UNH) crystals, and solutions. The sample preparation discussed in this test method focuses on fuel product material but may be used for uranium oxide or a uranium oxide alloy. Other preparation techniques may be used and some references are given. Purification of the uranium by anion-exchange extraction is not required for this test method, as it is required by other test methods such as radiochemistry and thermal ionization mass spectroscopy (TIMS). This test method is also described i...

American Society for Testing and Materials. Philadelphia

2000-01-01T23:59:59.000Z

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


221

Reports on investigations of uranium anomalies. National Uranium Resource Evaluation  

SciTech Connect (OSTI)

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

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

1982-10-01T23:59:59.000Z

222

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

E-Print Network [OSTI]

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. ...

Matthews, Isaac A

2010-01-01T23:59:59.000Z

223

Method for providing uranium articles with a corrosion resistant anodized coating  

DOE Patents [OSTI]

Uranium articles are provided with anodized oxide coatings in an aqueous solution of an electrolyte selected from the group consisting of potassium phosphate, potassium hydroxide, ammonium hydroxide, and a mixture of potassium tetraborate and boric acid. The uranium articles are anodized at a temperature greater than about 75.degree. C. with a current flow of less than about 0.036 A/cm.sup.2 of surface area while the pH of the solution is maintained in a range of about 2 to 11.5. The pH values of the aqueous solution and the low current density utilized during the electrolysis prevent excessive dissolution of the uranium and porosity in the film or watering. The relatively high temperature of the electrolyte bath inhibits hydration and the attendant deleterious pitting so as to enhance corrosion resistance of the anodized coating.

Waldrop, Forrest B. (Powell, TN); Washington, Charles A. (Oak Ridge, TN)

1982-01-01T23:59:59.000Z

224

Method for providing uranium articles with a corrosion-resistant anodized coating  

DOE Patents [OSTI]

Uranium articles are provided with anodized oxide coatings in an aqueous solution of an electrolyte selected from the group consisting of potassium phosphate, potassium hydroxide, ammonium hydroxide, and a mixture of potassium tetraborate and boric acid. The uranium articles are anodized at a temperature greater than about 75/sup 0/C with a current flow of less than about 0.036 A/cm/sup 2/ of surface area while the pH of the solution is maintained in a range of about 2 to 11.5. The pH values of the aqueous solution and the low current density utilized during the electrolysis prevent excessive dissolution of the uranium and porosity in the film or watering. The relatively high temperature of the electrolyte bath inhibits hydration and the attendant deleterious pitting so as to enhance corrosion resistance of the anodized coating.

Waldrop, F.B.; Washington, C.A.

1981-01-07T23:59:59.000Z

225

Bacterial Community Succession During in situ Uranium Bioremediation: Spatial Similarities Along Controlled Flow Paths  

E-Print Network [OSTI]

problem, and the use of depleted uranium and other heavyenvironmental hazard. Depleted uranium is weakly radioactive

Hwang, Chiachi

2009-01-01T23:59:59.000Z

226

Uranium 2009 resources, production and demand  

E-Print Network [OSTI]

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...

Organisation for Economic Cooperation and Development. Paris

2010-01-01T23:59:59.000Z

227

L'URANIUM ET LES ARMES L'URANIUM APPAUVRI. Pierre Roussel*  

E-Print Network [OSTI]

L'URANIUM ET LES ARMES � L'URANIUM APPAUVRI. Pierre Roussel* Institut de Physique Nucléaire, CNRS massivement dans la guerre du Golfe, des obus anti- chars ont été utilisés, avec des "charges d'uranium, avec une charge de 300 g d'uranium et tiré par des avions, l'autre de 120 mm de diamètre avec une

Boyer, Edmond

228

Dry process fluorination of uranium dioxide using ammonium bifluoride  

E-Print Network [OSTI]

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 ...

Yeamans, Charles Burnett, 1978-

2003-01-01T23:59:59.000Z

229

SHEEP MOUNTAIN URANIUM PROJECT CROOKS GAP, WYOMING  

E-Print Network [OSTI]

;PROJECT OVERVIEW ·Site Location·Site Location ·Fremont , Wyoming ·Existing Uranium Mine Permit 381C·Existing Uranium Mine Permit 381C ·Historical Operation ·Western Nuclear Crooks Gap Project ·Mined 1956 ­ 1988 and Open Pit Mining ·Current Mine Permit (381C) ·Updating POO, Reclamation Plan & Bond ·Uranium Recovery

230

Review of uranium bioassay techniques  

SciTech Connect (OSTI)

A variety of analytical techniques is available for evaluating uranium in excreta and tissues at levels appropriate for occupational exposure control and evaluation. A few (fluorometry, kinetic phosphorescence analysis, {alpha}-particle spectrometry, neutron irradiation techniques, and inductively-coupled plasma mass spectrometry) have also been demonstrated as capable of determining uranium in these materials at levels comparable to those which occur naturally. Sample preparation requirements and isotopic sensitivities vary widely among these techniques and should be considered carefully when choosing a method. This report discusses analytical techniques used for evaluating uranium in biological matrices (primarily urine) and limits of detection reported in the literature. No cost comparison is attempted, although references are cited which address cost. Techniques discussed include: {alpha}-particle spectrometry; liquid scintillation spectrometry, fluorometry, phosphorometry, neutron activation analysis, fission-track counting, UV-visible absorption spectrophotometry, resonance ionization mass spectrometry, and inductively-coupled plasma mass spectrometry. A summary table of reported limits of detection and of the more important experimental conditions associated with these reported limits is also provided.

Bogard, J.S.

1996-04-01T23:59:59.000Z

231

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

E-Print Network [OSTI]

, we are currently investigating the coordina- tion chemistry of uranium metal centers with classicalUranium Tris-aryloxide Derivatives Supported by Triazacyclononane: Engendering a Reactive Uranium, and Karsten Meyer* Contribution from the Department of Chemistry and Biochemistry, UniVersity of California

Meyer, Karsten

232

Statistical data of the uranium industry  

SciTech Connect (OSTI)

Statistical Data of the Uranium Industry is a compendium of information relating to US uranium reserves and potential resources and to exploration, mining, milling, and other activities of the uranium industry through 1981. The statistics are based primarily on data provided voluntarily by the uranium exploration, mining, and milling companies. The compendium has been published annually since 1968 and reflects the basic programs of the Grand Junction Area Office (GJAO) of the US Department of Energy. The production, reserves, and drilling information is reported in a manner which avoids disclosure of proprietary information.

none,

1982-01-01T23:59:59.000Z

233

Adsorptive Stripping Voltammetric Measurements of Trace Uranium...  

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

Measurements of Trace Uranium at the Bismuth Film Electrode. Abstract: Bismuth-coated carbon-fiber electrodes have been successfully applied for adsorptive-stripping...

234

Biogeochemical Processes In Ethanol Stimulated Uranium Contaminated...  

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

A laboratory incubation experiment was conducted with uranium contaminated subsurface sediment to assess the geochemical and microbial community response to ethanol amendment. A...

235

Colorimetric detection of uranium in water  

DOE Patents [OSTI]

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.

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

2012-03-13T23:59:59.000Z

236

Uranium Weapons Components Successfully Dismantled | National...  

National Nuclear Security Administration (NNSA)

Successfully Dismantled March 20, 2007 Uranium Weapons Components Successfully Dismantled Oak Ridge, TN Continuing its efforts to reduce the size of the U.S. nuclear weapons...

237

Review The Toxicity of Depleted Uranium  

E-Print Network [OSTI]

Abstract: Depleted uranium (DU) is an emerging environmental pollutant that is introduced into the environment primarily by military activity. While depleted uranium is less radioactive than natural uranium, it still retains all the chemical toxicity associated with the original element. In large doses the kidney is the target organ for the acute chemical toxicity of this metal, producing potentially lethal tubular necrosis. In contrast, chronic low dose exposure to depleted uranium may not produce a clear and defined set of symptoms. Chronic low-dose, or subacute, exposure to depleted uranium alters the appearance of milestones in developing organisms. Adult animals that were exposed to depleted uranium during development display persistent alterations in behavior, even after cessation of depleted uranium exposure. Adult animals exposed to depleted uranium demonstrate altered behaviors and a variety of alterations to brain chemistry. Despite its reduced level of radioactivity evidence continues to accumulate that depleted uranium, if ingested, may pose a radiologic hazard. The current state of knowledge concerning DU is discussed.

Wayne Briner

238

High strength and density tungsten-uranium alloys  

DOE Patents [OSTI]

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.

Sheinberg, Haskell (Los Alamos, NM)

1993-01-01T23:59:59.000Z

239

Distribution of uranium-bearing phases in soils from Fernald  

SciTech Connect (OSTI)

Electron beam techniques have been used to characterize uranium-contaminated soils and the Fernald Site, Ohio. Uranium particulates have been deposited on the soil through chemical spills and from the operation of an incinerator plant on the site. The major uranium phases have been identified by electron microscopy as uraninite, autunite, and uranium phosphite [U(PO{sub 3}){sub 4}]. Some of the uranium has undergone weathering resulting in the redistribution of uranium within the soil.

Buck, E.C.; Brown, N.R.; Dietz, N.L.

1993-12-31T23:59:59.000Z

240

Surface Decontamination of System Components in Uranium Conversion Plant at KAERI  

SciTech Connect (OSTI)

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

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

2003-02-25T23:59:59.000Z

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


241

SORPTION OF URANIUM, PLUTONIUM AND NEPTUNIUM ONTO SOLIDS PRESENT IN HIGH CAUSTIC NUCLEAR WASTE STORAGE TANKS  

SciTech Connect (OSTI)

Solids such as granular activated carbon, hematite and sodium phosphates, if present as sludge components in nuclear waste storage tanks, have been found to be capable of precipitating/sorbing actinides like plutonium, neptunium and uranium from nuclear waste storage tank supernatant liqueur. Thus, the potential may exists for the accumulation of fissile materials in such nuclear waste storage tanks during lengthy nuclear waste storage and processing. To evaluate the nuclear criticality safety in a typical nuclear waste storage tank, a study was initiated to measure the affinity of granular activated carbon, hematite and anhydrous sodium phosphate to sorb plutonium, neptunium and uranium from alkaline salt solutions. Tests with simulated and actual nuclear waste solutions established the affinity of the solids for plutonium, neptunium and uranium upon contact of the solutions with each of the solids. The removal of plutonium and neptunium from the synthetic salt solution by nuclear waste storage tank solids may be due largely to the presence of the granular activated carbon and transition metal oxides in these storage tank solids or sludge. Granular activated carbon and hematite also showed measurable affinity for both plutonium and neptunium. Sodium phosphate, used here as a reference sorbent for uranium, as expected, exhibited high affinity for uranium and neptunium, but did not show any measurable affinity for plutonium.

Oji, L; Bill Wilmarth, B; David Hobbs, D

2008-05-30T23:59:59.000Z

242

President Truman Increases Production of Uranium and Plutonium...  

National Nuclear Security Administration (NNSA)

Increases Production of Uranium and Plutonium October 09, 1950 President Truman Increases Production of Uranium and Plutonium Washington, DC President Truman approves a 1.4...

243

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...

244

Geochemical Controls on Contaminant Uranium in Vadose Hanford...  

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

Controls on Contaminant Uranium in Vadose Hanford Formation Sediments at the 200 Area and 300 Area, Hanford Site, Geochemical Controls on Contaminant Uranium in Vadose Hanford...

245

Microbial Reduction of Uranium under Iron- and Sulfate-reducing...  

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

Uranium under Iron- and Sulfate-reducing Conditions: Effect of Amended Goethite on Microbial Community Microbial Reduction of Uranium under Iron- and Sulfate-reducing Conditions:...

246

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

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

Uncertainty analysis of multi-rate kinetics of uranium desorption from sediments. Uncertainty analysis of multi-rate kinetics of uranium desorption from sediments. Abstract: A...

247

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

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

Most recently, LM visited 84 defense-related legacy uranium mine sites located within 11 uranium mining districts in 6 western states. At these sites, photographs and global...

248

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...

249

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

Energy Savers [EERE]

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

250

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

Office of Environmental Management (EM)

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

251

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...

252

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

Office of Environmental Management (EM)

Depleted Uranium Hexafluoride (DUF6) Fully Operational at the Portsmouth and Paducah Gaseous Diffusion Sites Depleted Uranium Hexafluoride (DUF6) Fully Operational at the...

253

Separation and Recovery of Uranium Metal from Spent Light Water Reactor Fuel via Electrolytic Reduction and Electrorefining  

SciTech Connect (OSTI)

A series of bench-scale experiments was performed in a hot cell at Idaho National Laboratory to demonstrate the separation and recovery of uranium metal from spent light water reactor (LWR) oxide fuel. The experiments involved crushing spent LWR fuel to particulate and separating it from its cladding. Oxide fuel particulate was then converted to metal in a series of six electrolytic reduction runs that were performed in succession with a single salt loading of molten LiCl – 1 wt% Li2O at 650 °C. Analysis of salt samples following the series of electrolytic reduction runs identified the diffusion of select fission products from the spent fuel to the molten salt electrolyte. The extents of metal oxide conversion in the post-test fuel were also quantified, including a nominal 99.7% conversion of uranium oxide to metal. Uranium metal was then separated from the reduced LWR fuel in a series of six electrorefining runs that were performed in succession with a single salt loading of molten LiCl-KCl-UCl3 at 500 °C. Analysis of salt samples following the series of electrorefining runs identified additional partitioning of fission products into the molten salt electrolyte. Analyses of the separated uranium metal were performed, and its decontamination factors were determined.

S. D. Herrmann; S. X. Li

2010-09-01T23:59:59.000Z

254

Structural Sequestration of Uranium in Bacteriogenic Manganese Oxides  

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

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255

Atomistic Simulations of Uranium Incorporation into Iron (Hydr)Oxides. |  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-Series to someone byDear Friend,ArthurMaterialsRibonuclease H.[0001]EMSL of

256

Standard test methods for chemical and mass spectrometric analysis of nuclear-grade gadolinium oxide (Gd2O3) powder  

E-Print Network [OSTI]

1.1 These test methods cover procedures for the chemical and mass spectrometric analysis of nuclear-grade gadolinium oxide powders to determine compliance with specifications. 1.2 The analytical procedures appear in the following order: Sections Carbon by Direct CombustionThermal Conductivity C1408 Test Method for Carbon (Total) in Uranium Oxide Powders and Pellets By Direct Combustion-Infrared Detection Method Total Chlorine and Fluorine by Pyrohydrolysis Ion Selective Electrode C1502 Test Method for Determination of Total Chlorine and Fluorine in Uranium Dioxide and Gadolinium Oxide Loss of Weight on Ignition 7-13 Sulfur by CombustionIodometric Titration Impurity Elements by a Spark-Source Mass Spectrographic C761 Test Methods for Chemical, Mass Spectrometric, Spectrochemical,Nuclear, and Radiochemical Analysis of Uranium Hexafluoride C1287 Test Method for Determination of Impurities In Uranium Dioxide By Inductively Coupled Plasma Mass Spectrometry Gadolinium Content in Gadolinium Oxid...

American Society for Testing and Materials. Philadelphia

2006-01-01T23:59:59.000Z

257

Texas plant will use new process to coproduce propylene oxide, MTBE  

SciTech Connect (OSTI)

Texaco Chemical Co. is building a $400 + million facility to produce 1.2 billion lb/year (14,000 b/d) methyl tertiary butyl ether (MTBE) and 400 million lb/year (about 500 metric tons/day) propylene oxide (PO). The facility-under construction at Port Neches, Tex.-will utilize a newly developed Texaco process that coproduces the two chemicals. The process produces propylene oxide and tertiary butyl alcohol (TBA) from the reaction of isobutane with oxygen in one step, then in a second step with propylene. The TBA is then reacted with methanol in a one-step process that synthesizes MTBE. The paper describes the Port Neches facilities, construction schedule, feedstocks, product uses, and auxiliary equipment.

Rhodes, A.K.

1993-08-30T23:59:59.000Z

258

Bioremediation of uranium contaminated soils and wastes  

SciTech Connect (OSTI)

Contamination of soils, water, and sediments by radionuclides and toxic metals from uranium mill tailings, nuclear fuel manufacturing and nuclear weapons production is a major concern. Studies of the mechanisms of biotransformation of uranium and toxic metals under various microbial process conditions has resulted in the development of two treatment processes: (1) stabilization of uranium and toxic metals with reduction in waste volume and (2) removal and recovery of uranium and toxic metals from wastes and contaminated soils. Stabilization of uranium and toxic metals in wastes is accomplished by exploiting the unique metabolic capabilities of the anaerobic bacterium, Clostridium sp. The radionuclides and toxic metals are solubilized by the bacteria directly by enzymatic reductive dissolution, or indirectly due to the production of organic acid metabolites. The radionuclides and toxic metals released into solution are immobilized by enzymatic reductive precipitation, biosorption and redistribution with stable mineral phases in the waste. Non-hazardous bulk components of the waste volume. In the second process uranium and toxic metals are removed from wastes or contaminated soils by extracting with the complexing agent citric acid. The citric-acid extract is subjected to biodegradation to recover the toxic metals, followed by photochemical degradation of the uranium citrate complex which is recalcitrant to biodegradation. The toxic metals and uranium are recovered in separate fractions for recycling or for disposal. The use of combined chemical and microbiological treatment process is more efficient than present methods and should result in considerable savings in clean-up and disposal costs.

Francis, A.J.

1998-12-31T23:59:59.000Z

259

Uranium Management - Preservation of a National Asset  

SciTech Connect (OSTI)

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.

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

2002-02-27T23:59:59.000Z

260

IPNS enriched uranium booster target  

SciTech Connect (OSTI)

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

Schulke, A.W. Jr.

1985-01-01T23:59:59.000Z

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


261

Molten-Salt Depleted-Uranium Reactor  

E-Print Network [OSTI]

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...

Dong, Bao-Guo; Gu, Ji-Yuan

2015-01-01T23:59:59.000Z

262

National Uranium Resource Evaluation, Tonopah quadrangle, Nevada  

SciTech Connect (OSTI)

The Tonopah Quadrangle, Nevada, was evaluated using National Uranium Resource Evaluation criteria to identify and delineate areas favorable for uranium deposits. Investigations included reconnaissance and detailed surface geologic and radiometric studies, geochemical sampling and evaluation, analysis and ground-truth followup of aerial radiometric and hydrogeochemical and stream-sediment reconnaissance data, and subsurface data evaluation. The results of these investigations indicate environments favorable for hydroallogenic uranium deposits in Miocene lacustrine sediments of the Big Smoky Valley west of Tonopah. The northern portion of the Toquima granitic pluton is favorable for authigenic uranium deposits. Environments considered unfavorable for uranium deposits include Quaternary sediments; intermediate and mafic volcanic and metavolcanic rocks; Mesozoic, Paleozoic, and Precambrian sedimentary and metasedimentary rocks; those plutonic rocks not included within favorable areas; and those felsic volcanic rocks not within the Northumberland and Mount Jefferson calderas.

Hurley, B W; Parker, D P

1982-04-01T23:59:59.000Z

263

Uranium in prehistoric Indian pottery  

E-Print Network [OSTI]

present in the sample, and the cross l section of the process (the measure of the probability of a neutron interacting with an uranium atom), In general, a daughter product 235 of U fission is analyzed on a detector which counts either gamma rays... for quantitative analysis of various elements on archaeological artifacts, Manganese has been determined in Mesoamerican pot sherds (Bennyhoff and Heizer 1965). A Pu-Be radioisotope neutron source with a flux of 4 x 10 4 -2 -1 neutrons cm sec was used...

Filberth, Ernest William

2012-06-07T23:59:59.000Z

264

2013 Uranium Marketing Annual Report  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"Click worksheet9,1,50022,3,,,,6,1,,781Title: Telephone:short version)ec 1827190List of Tables3 Uranium

265

2013 Uranium Marketing Annual Report  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"Click worksheet9,1,50022,3,,,,6,1,,781Title: Telephone:short version)ec 1827190List of Tables3 Uranium11

266

2013 Uranium Marketing Annual Report  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"Click worksheet9,1,50022,3,,,,6,1,,781Title: Telephone:short version)ec 1827190List of6,2009Uranium

267

2013 Uranium Marketing Annual Report  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"Click worksheet9,1,50022,3,,,,6,1,,781Title: Telephone:short version)ec 1827190List of6,2009UraniumNext

268

2013 Uranium Marketing Annual Report  

Gasoline and Diesel Fuel Update (EIA)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"Click worksheet9,1,50022,3,,,,6,1,,781Title: Telephone:short version)ec 1827190List of6,2009UraniumNext

269

U.S.Uranium Reserves  

Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

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270

2013 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 CenterFranconia, Virginia:FAQ < RAPID Jump to:SeadovCooperativeA2. World liquids consumption by region,Purchases2 U.S.Feed6a. Uranium

271

2013 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 CenterFranconia, Virginia:FAQ < RAPID Jump to:SeadovCooperativeA2. World liquids consumption by region,Purchases2 U.S.Feed6a.4. Uranium

272

Treatment of Uranium and Plutonium Solutions Generated in the Atalante Facility, France - 12004  

SciTech Connect (OSTI)

The Atalante complex operated by the French Alternative Energies and Atomic Energy Commission (CEA) at the Rhone Valley Research Center consolidates research programs on actinide chemistry, especially separation chemistry, processing for recycling spent fuel, and fabrication of actinide targets for innovative concepts in future nuclear systems. The design of future systems (Generation IV reactors, material recycling) will increase the uranium and plutonium flows in the facility, making it important to anticipate the stepped-up activity and provide Atalante with equipment dedicated to processing these solutions to obtain a mixed uranium-plutonium oxide that will be stored pending reuse. Ongoing studies for integral recycling of the actinides have highlighted the need for reserving equipment to produce actinides mixed oxide powder and also minor actinides bearing oxide for R and D purpose. To meet this double objective a new shielded line should be built in the facility and should be operational 6 years after go decision. The main functions of the new unit would be to receive, concentrate and store solutions, purify them, ensure group conversion of actinides and conversion of excess uranium. This new unit will be constructed in a completely refurbished building devoted to subcritical and safe geometry of the process equipments. (author)

Lagrave, Herve [French Alternative Energies and Atomic Energy Commission - CEA, Rhone Valley Research Center, BP 17171, 30207 Bagnols-sur-Ceze Cedex (France)

2012-07-01T23:59:59.000Z

273

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

SciTech Connect (OSTI)

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

Francis, C. W.

1993-09-01T23:59:59.000Z

274

Recovery of uranium by using new microorganisms isolated from North American uranium deposits  

SciTech Connect (OSTI)

Some attempts were made to remove uranium that may be present in refining effluents, mine tailings by using new microorganisms isolated from uranium deposits and peculiar natural environments. To screen microorganisms isolated from uranium deposits and peculiar natural environments in North America and Japan for maximal accumulation of uranium, hundreds of microorganisms were examined. Some microorganisms can accumulate about 500 mg (4.2 mEq) of uranium per gram of Microbial cells within 1 h. The uranium accumulation capacity of the cells exceeds that of commercially available chelating agents (2-3 mEq/g adsorbent). We attempted to recover uranium from uranium refining waste water by using new microorganisms. As a result, these microbial cells can recover trace amounts of uranium from uranium waste water with high efficiency. These strains also have a high accumulating ability for thorium. Thus, these new microorganisms can be used as an adsorbing agent for the removal of nuclear elements may be present in metallurgical effluents, mine tailings and other waste sources.

Sakaguchi, T.; Nakajima, A.; Tsuruta, T. [Miyazaki Medical College (Japan)

1995-12-31T23:59:59.000Z

275

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 (Me2PzĂ? ) led to forma- tion of an unprecedented homoleptic

276

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

SciTech Connect (OSTI)

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

NONE

1995-05-01T23:59:59.000Z

277

Technical Basis for Assessing Uranium Bioremediation Performance  

SciTech Connect (OSTI)

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.

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

2008-04-01T23:59:59.000Z

278

Flammability Analysis For Actinide Oxides Packaged In 9975 Shipping Containers  

SciTech Connect (OSTI)

Packaging options are evaluated for compliance with safety requirements for shipment of mixed actinide oxides packaged in a 9975 Primary Containment Vessel (PCV). Radiolytic gas generation rates, PCV internal gas pressures, and shipping windows (times to reach unacceptable gas compositions or pressures after closure of the PCV) are calculated for shipment of a 9975 PCV containing a plastic bottle filled with plutonium and uranium oxides with a selected isotopic composition. G-values for radiolytic hydrogen generation from adsorbed moisture are estimated from the results of gas generation tests for plutonium oxide and uranium oxide doped with curium-244. The radiolytic generation of hydrogen from the plastic bottle is calculated using a geometric model for alpha particle deposition in the bottle wall. The temperature of the PCV during shipment is estimated from the results of finite element heat transfer analyses.

Laurinat, James E.; Askew, Neal M.; Hensel, Steve J.

2013-03-21T23:59:59.000Z

279

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

E-Print Network [OSTI]

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

Duhovic, Selma

2012-01-01T23:59:59.000Z

280

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

E-Print Network [OSTI]

Uranium and Rare Earth Elements Using Biomass of Algae, Bioinorganic ChemistryRecovery of uranium from sea water. Chemistry & Industry (uranium recovery from seawater. Industrial & Engineering Chemistry

Rao, Linfeng

2011-01-01T23:59:59.000Z

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


281

Bacterial Community Succession During in situ Uranium Bioremediation: Spatial Similarities Along Controlled Flow Paths  

E-Print Network [OSTI]

problem, and the use of depleted uranium and other heavyenvironmental hazard. Depleted uranium is weakly radioactiveMB. (2004). Depleted and natural uranium: chemistry and

Hwang, Chiachi

2009-01-01T23:59:59.000Z

282

Crystal Chemistry of Early Actinides (Thorium, Uranium, and Neptunium) and Uranium Mesoporous Materials.  

E-Print Network [OSTI]

??Despite their considerable global importance, the structural chemistry of actinides remains understudied. Thorium and uranium fuel cycles are used in commercial nuclear reactors in India… (more)

Sigmon, Ginger E.

2010-01-01T23:59:59.000Z

283

Prokaryotic microorganisms in uranium mining waste piles and their interactions with uranium and other heavy metals.  

E-Print Network [OSTI]

??The influence of uranyl and sodium nitrate under aerobic and anaerobic conditions on the microbial community structure of a soil sample from the uranium mining… (more)

Geißler, Andrea

2007-01-01T23:59:59.000Z

284

The New Generation of Uranium In Situ Recovery Facilities: Design Improvements Should Reduce Radiological Impacts Relative to First Generation Uranium Solution Mining Plants  

SciTech Connect (OSTI)

In the last few years, there has been a significant increase in the demand for Uranium as historical inventories have been consumed and new reactor orders are being placed. Numerous mineralized properties around the world are being evaluated for Uranium recovery and new mining / milling projects are being evaluated and developed. Ore bodies which are considered uneconomical to mine by conventional methods such as tunneling or open pits, can be candidates for non-conventional recovery techniques, involving considerably less capital expenditure. Technologies such as Uranium In Situ Leaching / In Situ Recovery (ISL / ISR - also referred to as 'solution mining'), have enabled commercial scale mining and milling of relatively small ore pockets of lower grade, and are expected to make a significant contribution to overall world wide uranium supplies over the next ten years. Commercial size solution mining production facilities have operated in the US since the mid 1970's. However, current designs are expected to result in less radiological wastes and emissions relative to these 'first' generation plants (which were designed, constructed and operated through the 1980's). These early designs typically used alkaline leach chemistries in situ including use of ammonium carbonate which resulted in groundwater restoration challenges, open to air recovery vessels and high temperature calcining systems for final product drying vs the 'zero emissions' vacuum dryers as typically used today. Improved containment, automation and instrumentation control and use of vacuum dryers in the design of current generation plants are expected to reduce production of secondary waste byproduct material, reduce Radon emissions and reduce potential for employee exposure to uranium concentrate aerosols at the back end of the milling process. In Situ Recovery in the U.S. typically involves the circulation of groundwater, fortified with oxidizing (gaseous oxygen e.g) and complexing agents (carbon dioxide, e.g) into an ore body, solubilizing the uranium in situ, and then pumping the solutions to the surface where they are fed to a processing plant ( mill). Processing involves ion exchange and may also include precipitation, drying or calcining and packaging operations depending on facility specifics. This paper presents an overview of the ISR process and the health physics monitoring programs developed at a number of commercial scale ISL / ISR Uranium recovery and production facilities as a result of the radiological character of these processes. Although many radiological aspects of the process are similar to that of conventional mills, conventional-type tailings as such are not generated. However, liquid and solid byproduct materials may be generated and impounded. The quantity and radiological character of these by products are related to facility specifics. Some special monitoring considerations are presented which are required due to the manner in which radon gas is evolved in the process and the unique aspects of controlling solution flow patterns underground. The radiological character of these processes are described using empirical data collected from many operating facilities. Additionally, the major aspects of the health physics and radiation protection programs that were developed at these first generation facilities are discussed and contrasted to circumstances of the current generation and state of the art of uranium ISR technologies and facilities. In summary: This paper has presented an overview of in situ Uranium recovery processes and associated major radiological aspects and monitoring considerations. Admittedly, the purpose was to present an overview of those special health physics considerations dictated by the in situ Uranium recovery technology, to point out similarities and differences to conventional mill programs and to contrast these alkaline leach facilities to modern day ISR designs. As evidenced by the large number of ISR projects currently under development in the U.S. and worldwide, non conventional Uranium recovery techniques

Brown, S.H. [CHP, SHB INC., Centennial, Colorado (United States)

2008-07-01T23:59:59.000Z

285

In Situ Microbial Community Control of the Stability of Bio-reduced Uranium  

SciTech Connect (OSTI)

In aerobic aquifers typical of many Department of Energy (DOE) legacy waste sites, uranium is present in the oxidized U(VI) form which is more soluble and thus more mobile. Field experiments at the Old Rifle UMTRA site have demonstrated that biostimulation by electron donor addition (acetate) promotes biological U(VI) reduction (2). However, U(VI) reduction is reversible and oxidative dissolution of precipitated U(IV) after the cessation of electron donor addition remains a critical issue for the application of biostimulation as a treatment technology. Despite the potential for oxidative dissolution, field experiments at the Old Rifle site have shown that rapid reoxidation of bio-reduced uranium does not occur and U(VI) concentrations can remain at approximately 20% of background levels for more than one year. The extent of post-amendment U(VI) removal and the maintenance of bioreduced uranium may result from many factors including U(VI) sorption to iron-containing mineral phases, generation of H2S or FeS0.9, or the preferential sorption of U(VI) by microbial cells or biopolymers, but the processes controlling the reduction and in situ reoxidation rates are not known. To investigate the role of microbial community composition in the maintenance of bioreduced uranium, in-well sediment incubators (ISIs) were developed allowing field deployment of amended and native sediments during on-going experiments at the site. Field deployment of the ISIs allows expedient interrogation of microbial community response to field environmental perturbations and varying geochemical conditions.

Baldwin, Brett, R.; Peacock, Aaron, D.; Resch, Charles, T.; Arntzen, Evan; Smithgall, Amanda, N.; Pfiffner, Susan; Gan, M.; McKinley, James, P.; Long, Philip, E.; White, David, C.

2008-03-28T23:59:59.000Z

286

Depleted uranium disposition study -- Supplement, Revision 1  

SciTech Connect (OSTI)

The Department of Energy Office of Weapons and Materials Planning has requested a supplemental study to update the recent Depleted Uranium Disposition report. This supplemental study addresses new disposition alternatives and changes in status.

Becker, G.W.

1993-11-01T23:59:59.000Z

287

In situ remediation of uranium contaminated groundwater  

SciTech Connect (OSTI)

In an effort to develop cost-efficient techniques for remediating uranium contaminated groundwater at DOE Uranium Mill Tailing Remedial Action (UMTRA) sites nationwide, Sandia National Laboratories (SNL) deployed a pilot scale research project at an UMTRA site in Durango, CO. Implementation included design, construction, and subsequent monitoring of an in situ passive reactive barrier to remove Uranium from the tailings pile effluent. A reactive subsurface barrier is produced by emplacing a reactant material (in this experiment - various forms of metallic iron) in the flow path of the contaminated groundwater. Conceptually the iron media reduces and/or adsorbs uranium in situ to acceptable regulatory levels. In addition, other metals such as Se, Mo, and As have been removed by the reductive/adsorptive process. The primary objective of the experiment was to eliminate the need for surface treatment of tailing pile effluent. Experimental design, and laboratory and field preliminary results are discussed with regard to other potential contaminated groundwater treatment applications.

Dwyer, B.P.; Marozas, D.C. [Sandia National Labs., Albuquerque, NM (United States)

1997-12-31T23:59:59.000Z

288

In situ remediation of uranium contaminated groundwater  

SciTech Connect (OSTI)

In an effort to develop cost-efficient techniques for remediating uranium contaminated groundwater at DOE Uranium Mill Tailing Remedial Action (UMTRA) sites nationwide, Sandia National Laboratories (SNL) deployed a pilot scale research project at an UMTRA site in Durango, CO. Implementation included design, construction, and subsequent monitoring of an in situ passive reactive barrier to remove Uranium from the tailings pile effluent. A reactive subsurface barrier is produced by emplacing a reactant material (in this experiment various forms of metallic iron) in the flow path of the contaminated groundwater. Conceptually the iron media reduces and/or adsorbs uranium in situ to acceptable regulatory levels. In addition, other metals such as Se, Mo, and As have been removed by the reductive/adsorptive process. The primary objective of the experiment was to eliminate the need for surface treatment of tailing pile effluent. Experimental design, and laboratory and field results are discussed with regard to other potential contaminated groundwater treatment applications.

Dwyer, B.P.; Marozas, D.C.

1997-02-01T23:59:59.000Z

289

Process for reducing beta activity in uranium  

DOE Patents [OSTI]

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.

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

1986-01-01T23:59:59.000Z

290

Method of recovering uranium from aqueous solution  

SciTech Connect (OSTI)

Anion exchange resin derived from insoluble crosslinked polymers of vinyl benzyl chloride which are prepared by polymerizing vinyl benzyl chloride and a crosslinking monomer are particularly suitable in the treatment of uranium bearing leach liquors.

Albright, R.L.

1980-01-22T23:59:59.000Z

291

Innovative design of uranium startup fast reactors  

E-Print Network [OSTI]

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 ...

Fei, Tingzhou

2012-01-01T23:59:59.000Z

292

Process for reducing beta activity in uranium  

DOE Patents [OSTI]

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.

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

1985-04-11T23:59:59.000Z

293

EMSL - oxides  

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

oxides en Influence of Adsorption Site and Wavelength on the Photodesorption of NO from the (Fe,Cr)3O4(111) Mixed Oxide Surface. http:www.emsl.pnl.govemslwebpublications...

294

TRANSITION STATE FOR THE GAS-PHASE REACTION OF URANIUM HEXAFLUORIDE WITH WATER  

SciTech Connect (OSTI)

Density Functional Theory and small-core, relativistic pseudopotentials were used to look for symmetric and asymmetric transitions states of the gas-phase hydrolysis reaction of uranium hexafluoride, UF{sub 6}, with water. At the B3LYP/6-31G(d,p)/SDD level, an asymmetric transition state leading to the formation of a uranium hydroxyl fluoride, U(OH)F{sub 5}, and hydrogen fluoride was found with an energy barrier of +77.3 kJ/mol and an enthalpy of reaction of +63.0 kJ/mol (both including zero-point energy corrections). Addition of diffuse functions to all atoms except uranium led to only minor changes in the structure and relative energies of the reacting complex and transition state. However, a significant change in the product complex structure was found, significantly reducing the enthalpy of reaction to +31.9 kJ/mol. Similar structures and values were found for PBE0 and MP2 calculations with this larger basis set, supporting the B3LYP results. No symmetric transition state leading to the direct formation of uranium oxide tetrafluoride, UOF{sub 4}, was found, indicating that the reaction under ambient conditions likely includes several more steps than the mechanisms commonly mentioned. The transition state presented here appears to be the first published transition state for the important gas-phase reaction of UF{sub 6} with water.

Garrison, S; James Becnel, J

2008-03-18T23:59:59.000Z

295

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

SciTech Connect (OSTI)

In April 2001 the Department of Energy (DOE) and the Tennessee Valley Authority (TVA) signed an Interagency Agreement to transfer approximately 33 MT of off-specification (off-spec) highly enriched uranium (HEU) from DOE to TVA for conversion to commercial reactor fuel. Since that time additional surplus off-spec HEU material has been added to the program, making the total approximately 46 MT off-spec HEU. The disposition path for approximately half (23 MT) of this 46 MT of surplus HEU material, was down blending through the H-canyon facility at the Savannah River Site (SRS). The HEU is purified through the H-canyon processes, and then blended with natural uranium (NU) to form low enriched uranium (LEU) solution with a 4.95% U-235 isotopic content. This material was then transported to a TVA subcontractor who converted the solution to uranium oxide and then fabricated into commercial light water reactor (LWR) fuel. This fuel is now powering TVA reactors and supplying electricity to approximately 1 million households in the TVA region. There is still in excess of approximately 10 to 14 MT of off-spec HEU throughout the DOE complex or future foreign and domestic research reactor returns that could be recovered and down blended for use in either currently designed light water reactors, ?5% enriched LEU, or be made available for use in subsequent advanced 'fast' reactor fuel designs, ?19% LEU. (authors)

Magoulas, Virginia [Savannah River National Laboratory, Savannah River Site, Aiken, SC 29808 (United States)] [Savannah River National Laboratory, Savannah River Site, Aiken, SC 29808 (United States)

2013-07-01T23:59:59.000Z

296

Bioreduction and immobilization of uranium in situ: a case study at a USA Department of Energy radioactive waste site, Oak Ridge, Tennessee  

SciTech Connect (OSTI)

Bioremediation of uranium contaminated groundwater was tested by delivery of ethanol as an electron donor source to stimulate indigenous microbial bioactivity for reduction and immobilization of uranium in situ, followed by tests of stability of uranium sequestration in the bioreduced area via delivery of dissolved oxygen or nitrate at the US Department of energy's Integrated Field Research Challenge site located at Oak Ridge, Tennessee, USA. After long term treatment that spanned years, uranium in groundwater was reduced from 40-60 mg {center_dot} L{sup -1} to <0.03 mg {center_dot} L{sup -1}, below the USA EPA standard for drinking water. The bioreduced uranium was stable under anaerobic or anoxic conditions, but addition of DO and nitrate to the bioreduced zone caused U remobilization. The change in the microbial community and functional microorganisms related to uranium reduction and oxidation were characterized. The delivery of ethanol as electron donor stimulated the activities of indigenous microorganisms for reduction of U(VI) to U(IV). Results indicated that the immobilized U could be partially remobilized by D0 and nitrate via microbial activity. An anoxic environmental condition without nitrate is essential to maintain the stability of bioreduced uranium.

Wu, Weimin [Stanford University; Carley, Jack M [ORNL; Watson, David B [ORNL; Gu, Baohua [ORNL; Brooks, Scott C [ORNL; Kelly, Shelly D [Argonne National Laboratory (ANL); Kemner, Kenneth M [Argonne National Laboratory (ANL); Van Nostrand, Joy [University of Oklahoma, Norman; Wu, Liyou [University of Oklahoma, Norman; Zhou, Jizhong [University of Oklahoma, Norman; Luo, Jian [Georgia Institute of Technology; Cardenas, Erick [Michigan State University, East Lansing; Fields, Matthew Wayne [Miami University, Oxford, OH; Marsh, Terence [Michigan State University, East Lansing; Tiedje, James [Michigan State University, East Lansing; Green, Stefan [Florida State University; Kostka, Joel [Florida State University; Kitanidis, Peter K. [Stanford University; Jardine, Philip [University of Tennessee, Knoxville (UTK); Criddle, Craig [Stanford University

2011-01-01T23:59:59.000Z

297

The ultimate disposition of depleted uranium  

SciTech Connect (OSTI)

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

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

1991-12-31T23:59:59.000Z

298

BIOREMEDIATION OF URANIUM CONTAMINATED SOILS AND WASTES.  

SciTech Connect (OSTI)

Contamination of soils, water, and sediments by radionuclides and toxic metals from uranium mill tailings, nuclear fuel manufacturing and nuclear weapons production is a major concern. Studies of the mechanisms of biotransformation of uranium and toxic metals under various microbial process conditions has resulted in the development of two treatment processes: (i) stabilization of uranium and toxic metals with reduction in waste volume and (ii) removal and recovery of uranium and toxic metals from wastes and contaminated soils. Stabilization of uranium and toxic metals in wastes is accomplished by exploiting the unique metabolic capabilities of the anaerobic bacterium, Clostridium sp. The radionuclides and toxic metals are solubilized by the bacteria directly by enzymatic reductive dissolution, or indirectly due to the production of organic acid metabolites. The radionuclides and toxic metals released into solution are immobilized by enzymatic reductive precipitation, biosorption and redistribution with stable mineral phases in the waste. Non-hazardous bulk components of the waste such as Ca, Fe, K, Mg and Na released into solution are removed, thus reducing the waste volume. In the second process uranium and toxic metals are removed from wastes or contaminated soils by extracting with the complexing agent citric acid. The citric-acid extract is subjected to biodegradation to recover the toxic metals, followed by photochemical degradation of the uranium citrate complex which is recalcitrant to biodegradation. The toxic metals and uranium are recovered in separate fractions for recycling or for disposal. The use of combined chemical and microbiological treatment process is more efficient than present methods and should result in considerable savings in clean-up and disposal costs.

FRANCIS,A.J.

1998-09-17T23:59:59.000Z

299

Material property correlations for uranium mononitride  

E-Print Network [OSTI]

MATERIAL PROPERTY CORRELATIONS FOR URANIUM MONONITRIDE A Thesis by STEVEN LOWE HAYES Submitted to the Office of Graduate Studies of Texas ARM University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE August... 1989 Major Subject: Nuclear Engineering MATERIAL PROPERTY CORRELATIONS FOR URANIUM MONONITRIDE A Thesis by STEVEN LOWE HAYES Approved as to style and content by: K. L. Peddicord (Chair of Committee) R. R. Hart (Member) C. P. Burger (Member...

Hayes, Steven Lowe

2012-06-07T23:59:59.000Z

300

Electrochemical method of producing eutectic uranium alloy and apparatus  

DOE Patents [OSTI]

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.

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

1995-01-01T23:59:59.000Z

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


301

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

SciTech Connect (OSTI)

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

NONE

1995-07-05T23:59:59.000Z

302

Engineering assessment of inactive uranium mill tailings: Lakeview site, Lakeview, Oregon  

SciTech Connect (OSTI)

This 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 constitutes the most significant environmental impact, although windblown tailings and external gamma radiation also are factors. The three alternative actions presented in this engineering assessment include millsite decontamination with the addition of 3 m of stabilization cover material (Option I) and removal of the tailings to remote disposal sites and decontamination of the tailings site (Options II and III). Cost estimates range from about $6,000,000 for stabilization in-place, to about $7,500,000 for disposal at a distance of about 10 miles. Three alternatives for reprocessing the Lakeview tailings were examined: heap leaching, treatment at an existing mill, and reprocessing at a new conventional mill. The cost of the uranium recovered would be over $450/lb of U/sub 3/O/sub 8/ and hence reprocessing is not economical.

none,

1981-10-01T23:59:59.000Z

303

Extracting metals directly from metal oxides  

DOE Patents [OSTI]

A method of extracting metals directly from metal oxides by exposing the oxide to a supercritical fluid solvent containing a chelating agent is described. Preferably, the metal is an actinide or a lanthanide. More preferably, the metal is uranium, thorium or plutonium. The chelating agent forms chelates that are soluble in the supercritical fluid, thereby allowing direct removal of the metal from the metal oxide. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is selected from the group consisting of {beta}-diketones, halogenated {beta}-diketones, phosphinic acids, halogenated phosphinic acids, carboxylic acids, halogenated carboxylic acids, and mixtures thereof. In especially preferred embodiments, at least one of the chelating agents is fluorinated. The method provides an environmentally benign process for removing metals from metal oxides without using acids or biologically harmful solvents. The chelate and supercritical fluid can be regenerated, and the metal recovered, to provide an economic, efficient process. 4 figs.

Wai, C.M.; Smart, N.G.; Phelps, C.

1997-02-25T23:59:59.000Z

304

Extracting metals directly from metal oxides  

DOE Patents [OSTI]

A method of extracting metals directly from metal oxides by exposing the oxide to a supercritical fluid solvent containing a chelating agent is described. Preferably, the metal is an actinide or a lanthanide. More preferably, the metal is uranium, thorium or plutonium. The chelating agent forms chelates that are soluble in the supercritical fluid, thereby allowing direct removal of the metal from the metal oxide. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is selected from the group consisting of .beta.-diketones, halogenated .beta.-diketones, phosphinic acids, halogenated phosphinic acids, carboxylic acids, halogenated carboxylic acids, and mixtures thereof. In especially preferred embodiments, at least one of the chelating agents is fluorinated. The method provides an environmentally benign process for removing metals from metal oxides without using acids or biologically harmful solvents. The chelate and supercritical fluid can be regenerated, and the metal recovered, to provide an economic, efficient process.

Wai, Chien M. (Moscow, ID); Smart, Neil G. (Moscow, ID); Phelps, Cindy (Moscow, ID)

1997-01-01T23:59:59.000Z

305

Production of small uranium dioxide microspheres for cermet nuclear fuel using the internal gelation process  

SciTech Connect (OSTI)

The U.S. National Aeronautics and Space Administration (NASA) is developing a uranium dioxide (UO2)/tungsten cermet fuel for potential use as the nuclear cryogenic propulsion stage (NCPS). The first generation NCPS is expected to be made from dense UO2 microspheres with diameters between 75 and 150 m. Previously, the internal gelation process and a hood-scale apparatus with a vibrating nozzle were used to form gel spheres, which became UO2 kernels with diameters between 350 and 850 m. For the NASA spheres, the vibrating nozzle was replaced with a custom designed, two-fluid nozzle to produce gel spheres in the desired smaller size range. This paper describes the operational methodology used to make 3 kg of uranium oxide microspheres.

Collins, Robert T [ORNL] [ORNL; Collins, Jack Lee [ORNL] [ORNL; Hunt, Rodney Dale [ORNL] [ORNL; Ladd-Lively, Jennifer L [ORNL] [ORNL; Patton, Kaara K [ORNL] [ORNL; Hickman, Robert [NASA Marshall Space Flight Center, Huntsville, AL] [NASA Marshall Space Flight Center, Huntsville, AL

2014-01-01T23:59:59.000Z

306

Determination of kinetic coefficients for the simultaneous reduction of sulfate and uranium by Desulfovibrio desulfuricans bacteria  

SciTech Connect (OSTI)

Uranium contamination of groundwaters and surface waters near abandoned mill tailings piles is a serious concern in many areas of the western United States. Uranium usually exists in either the U(IV) or the U(VI) oxidation state. U(VI) is soluble in water and, as a result, is very mobile in the environment. U(IV), however, is generally insoluble in water and, therefore, is not subject to aqueous transport. In recent years, researchers have discovered that certain anaerobic microorganisms, such as the sulfate-reducing bacteria Desulfovibrio desulfuricans, can mediate the reduction of U(VI) to U(IV). Although the ability of this microorganism to reduce U(VI) has been studied in some detail by previous researchers, the kinetics of the reactions have not been characterized. The purpose of this research was to perform kinetic studies on Desulfovibrio desulficans bacteria during simultaneous reduction of sulfate and uranium and to determine the phase in which uranium exists after it has been reduced and precipitated from solution. The studies were conducted in a laboratory-scale chemostat under substrate-limited growth conditions with pyruvate as the substrate. Kinetic coefficients for substrate utilization and cell growth were calculated using the Monod equation. The maximum rate of substrate utilization (k) was determined to be 4.70 days{sup {minus}1} while the half-velocity constant (K{sub s}) was 140 mg/l COD. The yield coefficient (Y) was determined to be 0.17 mg cells/mg COD while the endogenous decay coefficient (k{sub d}) was calculated as 0.072 days{sup {minus}1}. After reduction, U(IV) Precipitated from solution in the uraninite (UO{sub 2}) phase. Uranium removal efficiency as high as 90% was achieved in the chemostat.

Tucker, M.D.

1995-05-01T23:59:59.000Z

307

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...

308

Fabrication and Characterization of Uranium-based High Temperature...  

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

Fabrication and Characterization of Uranium-based High Temperature Reactor Fuel June 01, 2013 The Uranium Fuel Development Laboratory is a modern R&D scale lab for the fabrication...

309

Assessments of long-term uranium supply availability  

E-Print Network [OSTI]

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 ...

Zaterman, Daniel R

2009-01-01T23:59:59.000Z

310

Prospects for the recovery of uranium from seawater  

E-Print Network [OSTI]

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 ...

Best, F. R.

1980-01-01T23:59:59.000Z

311

Monitoring Uranium Transformations Determined by the Evolution of Biogeochemical Processes  

SciTech Connect (OSTI)

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

Marsh, Terence L.

2013-07-30T23:59:59.000Z

312

Depleted Uranium in Kosovo Post-Conflict Environmental Assessment  

E-Print Network [OSTI]

2.1 UNEP’s role in post-conflict environmental assessment................................................9 2.2 Depleted uranium............................................................10

Unep Scientific; Mission Kosovo

313

Research, development and demonstration of nickel-zinc batteries for electric vehicle propulsion. Annual report, 1979. [70 W/lb  

SciTech Connect (OSTI)

This second annual report under Contract No. 31-109-39-4200 covers the period July 1, 1978 through August 31, 1979. The program demonstrates the feasibility of the nickel-zinc battery for electric vehicle propulsion. The program is divided into seven distinct but highly interactive tasks collectively aimed at the development and commercialization of nickel-zinc technology. These basic technical tasks are separator development, electrode development, product design and analysis, cell/module battery testing, process development, pilot manufacturing, and thermal management. A Quality Assurance Program has also been established. Significant progress has been made in the understanding of separator failure mechanisms, and a generic category of materials has been specified for the 300+ deep discharge (100% DOD) applications. Shape change has been reduced significantly. A methodology has been generated with the resulting hierarchy: cycle life cost, volumetric energy density, peak power at 80% DOD, gravimetric energy density, and sustained power. Generation I design full-sized 400-Ah cells have yielded in excess of 70 W/lb at 80% DOD. Extensive testing of cells, modules, and batteries is done in a minicomputer-based testing facility. The best life attained with electric vehicle-size cell components is 315 cycles at 100% DOD (1.0V cutoff voltage), while four-cell (approx. 6V) module performance has been limited to about 145 deep discharge cycles. The scale-up of processes for production of components and cells has progressed to facilitate component production rates of thousands per month. Progress in the area of thermal management has been significant, with the development of a model that accurately represents heat generation and rejection rates during battery operation. For the balance of the program, cycle life of > 500 has to be demonstrated in modules and full-sized batteries. 40 figures, 19 tables. (RWR)

Not Available

1980-06-01T23:59:59.000Z

314

Uranium Mill Tailings Remedial Action Project surface project management plan  

SciTech Connect (OSTI)

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.

Not Available

1994-09-01T23:59:59.000Z

315

Microbial Janitors: Enabling natural microbes to clean up uranium contamination  

E-Print Network [OSTI]

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

316

Plutonium recovery from spent reactor fuel by uranium displacement  

DOE Patents [OSTI]

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.

Ackerman, John P. (Downers Grove, IL)

1992-01-01T23:59:59.000Z

317

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

318

Bioremediation of Uranium Plumes with Nano-scale  

E-Print Network [OSTI]

(IV) (UO2[s], uraninite) Anthropogenic · Release of mill tailings during uranium mining - MobilizationBioremediation of Uranium Plumes with Nano-scale Zero-valent Iron Angela Athey Advisers: Dr. Reyes Undergraduate Student Fellowship Program April 15, 2011 #12;Main Sources of Uranium Natural · Leaching from

Fay, Noah

319

EPA Uranium Program Update Loren W. Setlow and  

E-Print Network [OSTI]

30, 2008 #12;2 Overview EPA Radiation protection program Uranium reports and abandoned mine lands and Liability Act #12;4 Uranium Reports and Abandoned Mine Lands Program ·Technologically Enhanced Naturally Occurring Radioactive Materials from Uranium Mining, Volume I: Mining and Reclamation Background (Revised

320

Soil to plant transfer of 238 Th on a uranium  

E-Print Network [OSTI]

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 The radioactive waste (e.g. tailings) produced by uranium mining activities contains a series of long

Hu, Qinhong "Max"

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


321

Plutonium recovery from spent reactor fuel by uranium displacement  

DOE Patents [OSTI]

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.

Ackerman, J.P.

1992-03-17T23:59:59.000Z

322

Composition of the U.S. DOE Depleted Uranium Inventory  

E-Print Network [OSTI]

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

Concentration Of Less

323

Modeling Uranium-Proton Ion Exchange in Biosorption  

E-Print Network [OSTI]

threatening heavy metals because of its high toxicity and some radioactivity. Excessive amounts of uranium seaweed biomass was used to remove the heavy metal uranium from the aqueous solution. Uranium biosorption the heavy metal uptake performance of different biosorbents.LangmuirandFreundlichmodelsoftengenerally fit

Volesky, Bohumil

324

Estimating terrestrial uranium and thorium by antineutrino flux measurements  

E-Print Network [OSTI]

of uranium and thorium concentrations in geological reservoirs relies largely on geochemi- cal modelEstimating 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

Mcdonough, William F.

325

A Geostatistical Study of the Uranium Deposit at Kvanefjeld,  

E-Print Network [OSTI]

with the geology. It is also shown that, although anisotropy exists, the uranium variation has a secondRisa-R-468 A Geostatistical Study of the Uranium Deposit at Kvanefjeld, The Ilimaussaq Intrusion A GEOSTATISTICAL STUDY OF THE URANIUM DEPOSIT AT KVANEFJELD, THE ILIMAUSSAQ INTRUSION, SOUTH GREENLAND Flemming

326

Depleted uranium plasma reduction system study  

SciTech Connect (OSTI)

A system life-cycle cost study was conducted of a preliminary design concept for a plasma reduction process for converting depleted uranium to uranium metal and anhydrous HF. The plasma-based process is expected to offer significant economic and environmental advantages over present technology. Depleted Uranium is currently stored in the form of solid UF{sub 6}, of which approximately 575,000 metric tons is stored at three locations in the U.S. The proposed system is preconceptual in nature, but includes all necessary processing equipment and facilities to perform the process. The study has identified total processing cost of approximately $3.00/kg of UF{sub 6} processed. Based on the results of this study, the development of a laboratory-scale system (1 kg/h throughput of UF6) is warranted. Further scaling of the process to pilot scale will be determined after laboratory testing is complete.

Rekemeyer, P.; Feizollahi, F.; Quapp, W.J.; Brown, B.W.

1994-12-01T23:59:59.000Z

327

Evaporation of Enriched Uranium Solutions Containing Organophosphates  

SciTech Connect (OSTI)

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

Pierce, R.A.

1999-03-18T23:59:59.000Z

328

Decarburization of uranium via electron beam processing  

SciTech Connect (OSTI)

For many commercial and military applications, the successive Vacuum Induction Melting of uranium metal in graphite crucibles results in a product which is out of specification in carbon. The current recovery method involves dissolution of the metal in acid and chemical purification. This is both expensive and generates mixed waste. A study was undertaken at Lawrence Livermore National Laboratory to investigate the feasibility of reducing the carbon content of uranium metal using electron beam techniques. Results will be presented on the rate and extent of carbon removal as a function of various operating parameters.

McKoon, R H

1998-10-23T23:59:59.000Z

329

Progress toward uranium scrap recycling via EBCHR  

SciTech Connect (OSTI)

A 250 kW electron beam cold hearth refining (EBCHR) melt furnace at Lawrence Livermore National Laboratory (LLNL) has been in operation for over a year producing 5.5 in.-diameter ingots of various uranium alloys. Production of in-specification uranium-6%-niobium (U-6Nb) alloy ingots has been demonstrated using virgin feedstock. A vibratory scrap feeder has been installed on the system and the ability to recycle chopped U-6Nb scrap has been established. A preliminary comparison of vacuum arc remelted (VAR) and electron beam (EB) melted product is presented.

McKoon, R.H.

1994-11-01T23:59:59.000Z

330

Variably Saturated Flow and Multicomponent Biogeochemical Reactive Transport Modeling of a Uranium Bioremediation Field Experiment  

SciTech Connect (OSTI)

Field experiments at a former uranium mill tailings site have identified the potential for stimulating indigenous bacteria to catalyze the conversion of aqueous uranium in the +6 oxidation state to immobile solid-associated uranium in the +4 oxidation state. This effectively removes uranium from solution resulting in groundwater concentrations below actionable standards. Three-dimensional, coupled variably-saturated flow and biogeochemical reactive transport modeling of a 2008 in situ uranium bioremediation field experiment is used to better understand the interplay of transport rates and biogeochemical reaction rates that determine the location and magnitude of key reaction products. A comprehensive reaction network, developed largely through previous 1-D modeling studies, was used to simulate the impacts on uranium behavior of pulsed acetate amendment, seasonal water table variation, spatially-variable physical (hydraulic conductivity, porosity) and geochemical (reactive surface area) material properties. A principal challenge is the mechanistic representation of biologically-mediated terminal electron acceptor process (TEAP) reactions whose products significantly alter geochemical controls on uranium mobility through increases in pH, alkalinity, exchangeable cations, and highly reactive reduction products. In general, these simulations of the 2008 Big Rusty acetate biostimulation field experiment in Rifle, Colorado confirmed previously identified behaviors including (1) initial dominance by iron reducing bacteria that concomitantly reduce aqueous U(VI), (2) sulfate reducing bacteria that become dominant after {approx}30 days and outcompete iron reducers for the acetate electron donor, (3) continuing iron-reducer activity and U(VI) bioreduction during dominantly sulfate reducing conditions, and (4) lower apparent U(VI) removal from groundwater during dominantly sulfate reducing conditions. New knowledge on simultaneously active metal and sulfate reducers has been incorporated into the modeling. In this case, an initially small population of slow growing sulfate reducers is active from the initiation of biostimulation. Three-dimensional, variably saturated flow modeling was used to address impacts of a falling water table during acetate injection. These impacts included a significant reduction in aquifer saturated thickness and isolation of residual reactants and products, as well as unmitigated uranium, in the newly unsaturated vadose zone. High permeability sandy gravel structures resulted in locally high flow rates in the vicinity of injection wells that increased acetate dilution. In downgradient locations, these structures created preferential flow paths for acetate delivery that enhanced local zones of TEAP reactivity and subsidiary reactions. Conversely, smaller transport rates associated with the lower permeability lithofacies (e.g., fine) and vadose zone were shown to limit acetate access and reaction. Once accessed by acetate, however, these same zones limited subsequent acetate dilution and provided longer residence times that resulted in higher concentrations of TEAP products when terminal electron donors and acceptors were not limiting. Finally, facies-based porosity and reactive surface area variations were shown to affect aqueous uranium concentration distributions; however, the ranges were sufficiently small to preserve general trends. Large computer memory and high computational performance were required to simulate the detailed coupled process models for multiple biogeochemical components in highly resolved heterogeneous materials for the 110-day field experiment and 50 days of post-biostimulation behavior. In this case, a highly-scalable subsurface simulator operating on 128 processor cores for 12 hours was used to simulate each realization. An equivalent simulation without parallel processing would have taken 60 days, assuming sufficient memory was available.

Yabusaki, Steven B.; Fang, Yilin; Williams, Kenneth H.; Murray, Christopher J.; Ward, Anderson L.; Dayvault, Richard; Waichler, Scott R.; Newcomer, Darrell R.; Spane, Frank A.; Long, Philip E.

2011-11-01T23:59:59.000Z

331

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

E-Print Network [OSTI]

Simplifying strong electronic correlations in uranium: Localized uranium heavy-fermion UM2Zn20 (M AtĂłmica, 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

Lawrence, Jon

332

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

SciTech Connect (OSTI)

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

NONE

1995-07-05T23:59:59.000Z

333

Competing retention pathways of uranium upon reaction with Fe(II)  

SciTech Connect (OSTI)

Biogeochemical retention processes, including adsorption, reductive precipitation, and incorporation into host minerals, are important in contaminant transport, remediation, and geologic deposition of uranium. Recent work has shown that U can become incorporated into iron (hydr)oxide minerals, with a key pathway arising from Fe(II)-induced transformation of ferrihydrite, (Fe(OH)3•nH2O) to goethite (?-FeO(OH)); this is a possible U retention mechanism in soils and sediments. Several key questions, however, remain unanswered regarding U incorporation into iron (hydr)oxides and this pathway’s contribution to U retention, including: (i) the competitiveness of U incorporation versus reduction to U(IV) and subsequent precipitation of UO2; (ii) the oxidation state of incorporated U; (iii) the effects of uranyl aqueous speciation on U incorporation; and, (iv) the mechanism of U incorporation. Here we use a series of batch reactions conducted at pH ~7, [U(VI)] from 1 to 170 ?M, [Fe(II)] from 0 to 3 mM, and [Ca] at 0 or 4 mM) coupled with spectroscopic examination of reaction products of Fe(II)-induced ferrihydrite transformation to address these outstanding questions. Uranium retention pathways were identified and quantified using extended x-ray absorption fine structure (EXAFS) spectroscopy, x-ray powder diffraction, x-ray photoelectron spectroscopy, and transmission electron microscopy. Analysis of EXAFS spectra showed that 14 to 89% of total U was incorporated into goethite, upon reaction with Fe(II) and ferrihydrite. Uranium incorporation was a particularly dominant retention pathway at U concentrations ? 50 ?M when either uranyl-carbonato or calcium-uranyl-carbonato complexes were dominant, accounting for 64 to 89% of total U. With increasing U(VI) and Fe(II) concentrations, U(VI) reduction to U(IV) became more prevalent, but U incorporation remained a functioning retention pathway. These findings highlight the potential importance of U(V) incorporation within iron oxides as a retention process of U across a wide range of biogeochemical environments and the sensitivity of uranium retention processes to operative (bio)geochemical conditions.

Massey, Michael S.; Lezama Pacheco, Juan S.; Jones, Morris; Ilton, Eugene S.; Cerrato, Jose M.; Bargar, John R.; Fendorf, Scott

2014-10-01T23:59:59.000Z

334

Geodatabase of the South Texas Uranium District  

E-Print Network [OSTI]

Uranium and its associated trace elements and radionuclides are ubiquitous in the South Texas Tertiary environment. Surface mining of this resource from the 1960s through the early 1980s at over sixty locations has left an extensive anthropological footprint (Fig. 1) in the lower Nueces and San Antonio river basins. Reclamation of mining initiated after 1975 has been under the regulatory authority of the Railroad Commission of Texas (RCT). However, mines that were active before the Texas Surface Mining Act of 1975 was enacted, and never reclaimed, are now considered abandoned. The Abandoned Mine Land Section of the RCT is currently reclaiming these pre-regulation uranium mines with funding from the federal government. The RCT monitors the overall effectiveness of this process through post-reclamation radiation and vegetative cover surveys, water quality testing, slope stability and erosion control monitoring. Presently a number of graduate and postgraduate students are completing research on the watershed and reservoir distribution of trace elements and radionuclides downstream of the South Texas Uranium District. The question remains as to whether the elevated levels of uranium, its associated trace elements and radiation levels in the South Texas environment are due to mining

Mark Beaman; William Wade Mcgee

335

The Quest for the Heaviest Uranium Isotope  

E-Print Network [OSTI]

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.

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

2012-01-17T23:59:59.000Z

336

The multiphoton ionization of uranium hexafluoride  

SciTech Connect (OSTI)

Multiphoton ionization (MPI) time-of-flight mass spectroscopy and photoelectron spectroscopy studies of UF{sub 6} have been conducted using focused light from the Nd:YAG laser fundamental ({lambda}=1064 nm) and its harmonics ({lambda}=532, 355, or 266 nm), as well as other wavelengths provided by a tunable dye laser. The MPI mass spectra are dominated by the singly and multiply charged uranium ions rather than by the UF{sub x}{sup +} fragment ions even at the lowest laser power densities at which signal could be detected. The laser power dependence of U{sup n+} ions signals indicates that saturation can occur for many of the steps required for their ionization. In general, the doubly-charged uranium ion (U{sup 2+}) intensity is much greater than that of the singly-charged uranium ion (U{sup +}). For the case of the tunable dye laser experiments, the U{sup n+} (n = 1- 4) wavelength dependence is relatively unstructured and does not show observable resonance enhancement at known atomic uranium excitation wavelengths. The dominance of the U{sup 2+} ion and the absence or very small intensities of UF{sub x}{sup +} fragments, along with the unsaturated wavelength dependence, indicate that mechanisms may exist other than ionization of bare U atoms after the stepwise photodissociation of F atoms from the parent molecule.

Armstrong, D.P. (Oak Ridge K-25 Site, TN (United States). UEO Enrichment Technical Operations Div.)

1992-05-01T23:59:59.000Z

337

Radiological health aspects of uranium milling  

SciTech Connect (OSTI)

This report describes the operation of conventional and unconventional uranium milling processes, the potential for occupational exposure to ionizing radiation at the mill, methods for radiological safety, methods of evaluating occupational radiation exposures, and current government regulations for protecting workers and ensuring that standards for radiation protection are adhered to. In addition, a survey of current radiological health practices is summarized.

Fisher, D.R.; Stoetzel, G.A.

1983-05-01T23:59:59.000Z

338

Investigation of Trace Uranium in Biological Matrices  

E-Print Network [OSTI]

complex. As a result, the data varies in its breadth and quality due to the variety of sources.[41-44] Additional studies have been undertaken to understand the effects of using depleted uranium munitions in war and the accompanying exposures.[45...

Miller, James Christopher

2013-05-31T23:59:59.000Z

339

Thermochemical Modeling of the Uranium-Cerium-Oxygen System  

SciTech Connect (OSTI)

The objective of the Fuel Cycle R&D Program, Advanced Fuels campaign is to provide the research and development necessary to develop low loss, high quality nuclear fuels for ultra-high burnup reactor operation. Primary work in this area will be focused on the ceramic and metallic fuel systems. The goal of the current work is to enhance the understanding of ceramic nuclear fuel thermochemistry to support fuel research and development efforts. The thermochemical behavior of oxide nuclear fuel under irradiation is dependent on the oxygen to metal ratio (O:M). In fluorite-structured fuel, the actinide metal cation is bonded with {approx}2 oxygen atoms on a crystal lattice and as the metal atoms fission, fission fragments and free oxygen are created. The resulting fission fragments will contain some oxide forming elements, however these are insufficient to bind to all the liberated oxygen and therefore, there is an average increase in O:M with fuel burnup. Some of the fission products also form species that will migrate to and react with the cladding surface in a phenomenon known as Fuel Clad Chemical Interaction (FCCI). Cladding corrosion is life-limiting so it is desirable to understand influencing factors, such as oxide thermochemistry, which can be used to guide the design and fabrication of higher burn up fuel. A phased oxide fuel thermochemical model development effort is underway within the Advanced Fuels Campaign. First models of binary oxide systems are developed. For nuclear fuel system this means U-O and transuranic systems such as Pu-O, Np-O and Am-O. Next, the binary systems will be combined to form pseudobinary systems such as U-Pu-O, etc. The model development effort requires the use of data to allow optimization based on known thermochemical parameters as a function of composition and temperature. Available data is mined from the literature and supplemented by experimental work as needed. Due to the difficulty of performing fuel fabrication development with actinide materials, fundamental studies with uranium are performed using surrogate materials as stand-ins for transuranic elements. In most cases, cerium can be used as a suitable substitute for plutonium when performing O:M and sintering kinetics studies because of identical valence states. Differences exist between the magnitude of reported thermodynamic data of (U,Pu)O{sub x} and (U,Ce)O{sub x}, however the change in oxygen potential versus O:M follows the same trend for both systems. Cerium is also a major fission product element, and thus understanding its behavior in fuel is an important issue as well.

Voit, Stewart L [ORNL; Besmann, Theodore M [ORNL

2010-10-01T23:59:59.000Z

340

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

E-Print Network [OSTI]

researchers from uranium chemistry. Fortunately, despitescarce in uranium coordination chemistry. A more detailedligands for uranium coordination chemistry. Figure 4-2.

Lam, Oanh Phi

2010-01-01T23:59:59.000Z

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


341

Warm Water Oxidation Verification - Scoping and Stirred Reactor Tests  

SciTech Connect (OSTI)

Scoping tests to evaluate the effects of agitation and pH adjustment on simulant sludge agglomeration and uranium metal oxidation at {approx}95 C were performed under Test Instructions(a,b) and as per sections 5.1 and 5.2 of this Test Plan prepared by AREVA. (c) The thermal testing occurred during the week of October 4-9, 2010. The results are reported here. For this testing, two uranium-containing simulant sludge types were evaluated: (1) a full uranium-containing K West (KW) container sludge simulant consisting of nine predominant sludge components; (2) a 50:50 uranium-mole basis mixture of uraninite [U(IV)] and metaschoepite [U(VI)]. This scoping study was conducted in support of the Sludge Treatment Project (STP) Phase 2 technology evaluation for the treatment and packaging of K-Basin sludge. The STP is managed by CH2M Hill Plateau Remediation Company (CHPRC) for the U.S. Department of Energy. Warm water ({approx}95 C) oxidation of sludge, followed by immobilization, has been proposed by AREVA and is one of the alternative flowsheets being considered to convert uranium metal to UO{sub 2} and eliminate H{sub 2} generation during final sludge disposition. Preliminary assessments of warm water oxidation have been conducted, and several issues have been identified that can best be evaluated through laboratory testing. The scoping evaluation documented here was specifically focused on the issue of the potential formation of high strength sludge agglomerates at the proposed 95 C process operating temperature. Prior hydrothermal tests conducted at 185 C produced significant physiochemical changes to genuine sludge, including the formation of monolithic concretions/agglomerates that exhibited shear strengths in excess of 100 kPa (Delegard et al. 2007).

Braley, Jenifer C.; Sinkov, Sergey I.; Delegard, Calvin H.; Schmidt, Andrew J.

2011-06-15T23:59:59.000Z

342

From Nanowires to Biofilms: An Exploration of Novel Mechanisms of Uranium Transformation Mediated by Geobacter Bacteria  

SciTech Connect (OSTI)

One promising strategy for the in situ bioremediation of radioactive groundwater contaminants that has been identified by the SBR Program is to stimulate the activity of dissimilatory metal-reducing microorganisms to reductively precipitate uranium and other soluble toxic metals. The reduction of U(VI) and other soluble contaminants by Geobacteraceae is directly dependent on the reduction of Fe(III) oxides, their natural electron acceptor, a process that requires the expression of Geobacter’s conductive pili (pilus nanowires). Expression of conductive pili by Geobacter cells leads to biofilm development on surfaces and to the formation of suspended biogranules, which may be physiological closer to biofilms than to planktonic cells. Biofilm development is often assumed in the subsurface, particularly at the matrix-well screen interface, but evidence of biofilms in the bulk aquifer matrix is scarce. Our preliminary results suggest, however, that biofilms develop in the subsurface and contribute to uranium transformations via sorption and reductive mechanisms. In this project we elucidated the mechanism(s) for uranium immobilization mediated by Geobacter biofilms and identified molecular markers to investigate if biofilm development is happening in the contaminated subsurface. The results provided novel insights needed in order to understand the metabolic potential and physiology of microorganisms with a known role in contaminant transformation in situ, thus having a significant positive impact in the SBR Program and providing novel concept to monitor, model, and predict biological behavior during in situ treatments.

REGUERA, GEMMA [Michigan State University

2014-01-16T23:59:59.000Z

343

The burnup dependence of light water reactor spent fuel oxidation  

SciTech Connect (OSTI)

Over the temperature range of interest for dry storage or for placement of spent fuel in a permanent repository under the conditions now being considered, UO{sub 2} is thermodynamically unstable with respect to oxidation to higher oxides. The multiple valence states of uranium allow for the accommodation of interstitial oxygen atoms in the fuel matrix. A variety of stoichiometric and nonstoichiometric phases is therefore possible as the fuel oxidizers from UO{sub 2} to higher oxides. The oxidation of UO{sub 2} has been studied extensively for over 40 years. It has been shown that spent fuel and unirradiated UO{sub 2} oxidize via different mechanisms and at different rates. The oxidation of LWR spent fuel from UO{sub 2} to UO{sub 2.4} was studied previously and is reasonably well understood. The study presented here was initiated to determine the mechanism and rate of oxidation from UO{sub 2.4} to higher oxides. During the early stages of this work, a large variability in the oxidation behavior of samples oxidized under nearly identical conditions was found. Based on previous work on the effect of dopants on UO{sub 2} oxidation and this initial variability, it was hypothesized that the substitution of fission product and actinide impurities for uranium atoms in the spent fuel matrix was the cause of the variable oxidation behavior. Since the impurity concentration is roughly proportional to the burnup of a specimen, the oxidation behavior of spent fuel was expected to be a function of both temperature and burnup. This report (1) summarizes the previous oxidation work for both unirradiated UO{sub 2} and spent fuel (Section 2.2) and presents the theoretical basis for the burnup (i.e., impurity concentration) dependence of the rate of oxidation (Sections 2.3, 2.4, and 2.5), (2) describes the experimental approach (Section 3) and results (Section 4) for the current oxidation tests on spent fuel, and (3) establishes a simple model to determine the activation energies associated with spent fuel oxidation (Section 5).

Hanson, B.D.

1998-07-01T23:59:59.000Z

344

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

SciTech Connect (OSTI)

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

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

2003-08-01T23:59:59.000Z

345

Elucidating Bioreductive Transformations within Physically Complex Media: Impact on the Fate and Transport of Uranium and Chromium  

SciTech Connect (OSTI)

In situ stabilization (inclusive of natural attenuation) of toxic metals and radionuclides is an attractive approach for remediating many contaminated DOE sites. By immobilizing toxic metals and radionuclides in place, the removal of contaminated water to the surface for treatment as well as the associated disposal costs are avoided. To enhance in situ remediaton, microbiological reductive stabilization of contaminant metals has been, and continues to be, actively explored. It is likely that surface and subsurface microbial activity can alter the redox state of toxic metals and radionuclides, either directly or indirectly, so they are rendered immobile. Furthermore, anaerobic bacterial metabolic products will help to buffer pulses of oxidation, typically from fluxes of nitrate or molecular oxygen, and thus may stabilize reduced contaminants from oxidative mobilization. Uranium and chromium are two elements of particular concern within the DOE complex that, owing to their abundance and toxicity, appear well suited for biologically mediated reductive stabilization. Subsurface microbial activity can alter the redox state of toxic metals and radionuclides, rending them immobile. Imparting an important criterion on the probability that contaminants will undergo reductive stabilization, however, is the chemical and physical heterogeneity of the media. Our research first examined microbially induced transformation of iron (hydr)oxide minerals and their impact on contaminant attenuation. We revealed that in intricate cascade of geochemical reactions is induced by microbially produced Fe(II), and that during transformation contaminants such as U(VI) can be incorporated into the structure, and a set of Fe(II) bearing solids capable of reducing Cr(VI) and stabilizing resulting Cr(III). We also note, however, that common subsurface constituents such as phosphate can modify iron oxide transformation pathways and thus impact contaminant sequestration—affecting both Cr and U stabilization. We extended our work to explore factors controlling the sequestration of uranium in the subsurface, with a particular emphasis on mineralogic and geochemical complexity. We reveal that one of the primary factors controlling uranium reduction, via both biological and chemical pathways, is the aqueous speciation of U(VI). Specifically, ternary calcium-uranyl-carbonato complexes stabilize U(VI) relative to reduction. However, countering the lack of reduction, we note a novel sequestration pathway in which the U(VI), as the uranate ion, is incorporated into the structure of transformation iron oxides; magnetite and goethite, both products of Fe(II) induced transformation of ferrihydrite, harbor appreciable quantities of uranium. In sum, our results provide important information on predicting and potentially controlling the migration of chromium and uranium within the DOE complex.

Scott Fendorf; Chris Francis; Phil Jardine; Shawn Benner

2009-03-01T23:59:59.000Z

346

Gas Generation from K East Basin Sludges and Irradiated Metallic Uranium Fuel Particles Series III Testing  

SciTech Connect (OSTI)

The path forward for managing of Hanford K Basin sludge calls for it to be packaged, shipped, and stored at T Plant until final processing at a future date. An important consideration for the design and cost of retrieval, transportation, and storage systems is the potential for heat and gas generation through oxidation reactions between uranium metal and water. This report, the third in a series (Series III), describes work performed at the Pacific Northwest National Laboratory (PNNL) to assess corrosion and gas generation from irradiated metallic uranium particles (fuel particles) with and without K Basin sludge addition. The testing described in this report consisted of 12 tests. In 10 of the tests, 4.3 to 26.4 g of fuel particles of selected size distribution were placed into 60- or 800-ml reaction vessels with 0 to 100 g settled sludge. In another test, a single 3.72-g fuel fragment (i.e., 7150-mm particle) was placed in a 60 ml reaction vessel with no added sludge. The twelfth test contained only sludge. The fuel particles were prepared by crushing archived coupons (samples) from an irradiated metallic uranium fuel element. After loading the sludge materials (whether fuel particles, mixtures of fuel particles and sludge, or sludge-only) into reaction vessels, the solids were covered with an excess of K Basin water, the vessels closed and connected to a gas measurement manifold, and the vessels back-flushed with inert neon cover gas. The vessels were then heated to a constant temperature. The gas pressures and temperatures were monitored continuously from the times the vessels were purged. Gas samples were collected at various times during the tests, and the samples analyzed by mass spectrometry. Data on the reaction rates of uranium metal fuel particles with water as a function of temperature and particle size were generated. The data were compared with published studies on metallic uranium corrosion kinetics. The effects of an intimate overlying sludge layer (''blanket'') on the uranium metal corrosion rates were also evaluated.

Schmidt, Andrew J.; Delegard, Calvin H.; Bryan, Samuel A.; Elmore, Monte R.; Sell, Rachel L.; Silvers, Kurt L.; Gano, Susan R.; Thornton, Brenda M.

2003-08-01T23:59:59.000Z

347

Destruction of plutonium using non-uranium fuels in pressurized water reactor peripheral assemblies  

SciTech Connect (OSTI)

This thesis examines and confirms the feasibility of using non-uranium fuel in a pressurized water reactor (PWR) radial blanket to eliminate plutonium of both weapons and civilian origin. In the equilibrium cycle, the periphery of the PWR is loaded with alternating fresh and once burned non-uranium fuel assemblies, with the interior of the core comprised of conventional three batch UO{sub 2} assemblies. Plutonium throughput is such that there is no net plutonium production: production in the interior is offset by destruction in the periphery. Using this approach a 50 MT WGPu inventory could be eliminated in approximately 400 reactor years of operation. Assuming all other existing constraints were removed, the 72 operating US PWRs could disposition 50 MT of WGPu in 5.6 years. Use of a low fissile loading plutonium-erbium inert-oxide-matrix composition in the peripheral assemblies essentially destroys 100% of the {sup 239}Pu and {ge}90% {sub total}Pu over two 18 month fuel cycles. Core radial power peaking, reactivity vs EFPD profiles and core average reactivity coefficients were found to be comparable to standard PWR values. Hence, minimal impact on reload licensing is anticipated. Examination of potential candidate fuel matrices based on the existing experience base and thermo-physical properties resulted in the recommendation of three inert fuel matrix compositions for further study: zirconia, alumina and TRISO particle fuels. Objective metrics for quantifying the inherent proliferation resistance of plutonium host waste and fuel forms are proposed and were applied to compare the proposed spent WGPu non-uranium fuel to spent WGPu MOX fuels and WGPu borosilicate glass logs. The elimination disposition option spent non-uranium fuel product was found to present significantly greater barriers to proliferation than other plutonium disposal products.

Chodak, P. III

1996-05-01T23:59:59.000Z

348

Electrodic voltages accompanying stimulated bioremediation of a uranium-contaminated aquifer  

SciTech Connect (OSTI)

The inability to track the products of subsurface microbial activity during stimulated bioremediation has limited its implementation. We used spatiotemporal changes in electrodic potentials (EP) to track the onset and persistence of stimulated sulfate-reducing bacteria in a uranium-contaminated aquifer undergoing acetate amendment. Following acetate injection, anomalous voltages approaching -900 mV were measured between copper electrodes within the aquifer sediments and a single reference electrode at the ground surface. Onset of EP anomalies correlated in time with both the accumulation of dissolved sulfide and the removal of uranium from groundwater. The anomalies persisted for 45 days after halting acetate injection. Current-voltage and current-power relationships between measurement and reference electrodes exhibited a galvanic response, with a maximum power density of 10 mW/m{sup 2} during sulfate reduction. We infer that the EP anomalies resulted from electrochemical differences between geochemically reduced regions and areas having higher oxidation potential. Following the period of sulfate reduction, EP values ranged from -500 to -600 mV and were associated with elevated concentrations of ferrous iron. Within 10 days of the voltage decrease, uranium concentrations rebounded from 0.2 to 0.8 {mu}M, a level still below the background value of 1.5 {mu}M. These findings demonstrate that EP measurements provide an inexpensive and minimally invasive means for monitoring the products of stimulated microbial activity within aquifer sediments and are capable of verifying maintenance of redox conditions favorable for the stability of bioreduced contaminants, such as uranium.

Williams, K.H.; N'Guessan, A.L.; Druhan, J.; Long, P.E.; Hubbard, S.S.; Lovley, D.R.; Banfield, J.F.

2009-11-15T23:59:59.000Z

349

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

SciTech Connect (OSTI)

Resonance Ionization Mass Spectrometry (RIMS) has been developed as a method to measure relative uranium isotope abundances. In this approach, RIMS is used as an element-selective ionization process to provide a distinction between uranium atoms and potential isobars without the aid of chemical purification and separation. We explore the laser parameters critical to the ionization process and their effects on the measured isotope ratio. Specifically, the use of broad bandwidth lasers with automated feedback control of wavelength was applied to the measurement of {sup 235}U/{sup 238}U ratios to decrease laser-induced isotopic fractionation. By broadening the bandwidth of the first laser in a 3-color, 3-photon ionization process from a bandwidth of 1.8 GHz to about 10 GHz, the variation in sequential relative isotope abundance measurements decreased from >10% to less than 0.5%. This procedure was demonstrated for the direct interrogation of uranium oxide targets with essentially no sample preparation. A rate equation model for predicting the relative ionization probability has been developed to study the effect of variation in laser parameters on the measured isotope ratio. This work demonstrates that RIMS can be used for the robust measurement of uranium isotope ratios.

Isselhardt, B H

2011-09-06T23:59:59.000Z

350

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

SciTech Connect (OSTI)

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

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

2012-03-01T23:59:59.000Z

351

Contents of environmental assessments prepared for the Uranium Mill Tailings Remedial Action Project  

SciTech Connect (OSTI)

This document presents two versions of the outline for the environmental assessments (EAS) to be prepared for the Uranium Mill Tailings Remedial Action (UMTRA) Project. The first displays the basic structure of the assessments; it lists only the titles of sections. The second is a guide to the contents of the assessments which provides, under each title, a brief summary of contents. The outline is intended to comply with the planning requirements (40 CFR Part 1501) and the definitions of terms (40-' CFR Part 1508) established by the Council on Environmental Quality as well as DOE order 5440.lB (Implementation of the National Environmental Policy Act), and compliance with Floodplain/Wetlands Environmental Review Requirements (10 CFR Part 1022). These requirements and definitions are implicitly part of the outline. The outline presented in this document will guide the preparation of EAs. The UMTRA Project EAs will be used in determining whether the DOE should prepare an environmental impact statement or a finding of no significant impact for the actions at each of the sites. If no impact statement is necessary, the environmental assessment for that site will aid the DOE in complying with the National Environmental Policy Act before beginning remedial actions. If an impact statement is needed, the assessment will aid its preparation. These purposes, established by the Council on Environmental Quality in 40 CFR Part 1508.9(a), have guided the construction of the outline presented in this document. Remedial actions at each site will include the cleanup of properties in the vicinity of the tailings sites that have been contaminated by the tailings.

Not Available

1986-01-01T23:59:59.000Z

352

Contents of environmental assessments prepared for the Uranium Mill Tailings Remedial Action Project  

SciTech Connect (OSTI)

This document presents two versions of the outline for the environmental assessments (EAS) to be prepared for the Uranium Mill Tailings Remedial Action (UMTRA) Project. The first displays the basic structure of the assessments; it lists only the titles of sections. The second is a guide to the contents of the assessments which provides, under each title, a brief summary of contents. The outline is intended to comply with the planning requirements (40 CFR Part 1501) and the definitions of terms (40-` CFR Part 1508) established by the Council on Environmental Quality as well as DOE order 5440.lB (Implementation of the National Environmental Policy Act), and compliance with Floodplain/Wetlands Environmental Review Requirements (10 CFR Part 1022). These requirements and definitions are implicitly part of the outline. The outline presented in this document will guide the preparation of EAs. The UMTRA Project EAs will be used in determining whether the DOE should prepare an environmental impact statement or a finding of no significant impact for the actions at each of the sites. If no impact statement is necessary, the environmental assessment for that site will aid the DOE in complying with the National Environmental Policy Act before beginning remedial actions. If an impact statement is needed, the assessment will aid its preparation. These purposes, established by the Council on Environmental Quality in 40 CFR Part 1508.9(a), have guided the construction of the outline presented in this document. Remedial actions at each site will include the cleanup of properties in the vicinity of the tailings sites that have been contaminated by the tailings.

Not Available

1986-01-01T23:59:59.000Z

353

In-Well Sediment Incubators to Evaluate Microbial Community Stability and Dynamics following Bioimmobilization of Uranium  

SciTech Connect (OSTI)

An in-situ incubation device (ISI) was developed in order to investigate the stability and dynamics of sediment associated microbial communities to prevailing subsurface oxidizing or reducing conditions. Here we describe the use of these devices at the Old Rifle Uranium Mill Tailings Remedial Action (UMTRA) site. During the 7 month deployment oxidized Rifle aquifer background sediments (RABS) were deployed in previously biostimulated wells under iron reducing conditions, cell densities of known iron reducing bacteria including Geobacteraceae increased significantly showing the microbial community response to local subsurface conditions. PLFA profiles of RABS following in situ deployment were strikingly similar to those of adjacent sediment cores suggesting ISI results could be extrapolated to the native material of the test plots. Results for ISI deployed reduced sediments showed only slight changes in community composition and pointed toward the ability of the ISIs to monitor microbial community stability and response to subsurface conditions.

Baldwin, Brett R.; Peacock, Aaron D.; Gan, M.; Resch, Charles T.; Arntzen, Evan V.; Smithgall, A. N.; Pfiffner, S.; Freifeld, Barry M.; White, D. C.; Long, Philip E.

2009-09-23T23:59:59.000Z

354

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

SciTech Connect (OSTI)

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)

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

2012-07-01T23:59:59.000Z

355

Dry air oxidation kinetics of K-Basin spent nuclear fuel  

SciTech Connect (OSTI)

The safety and process analyses of the proposed Integrated Process Strategy (IPS) to move the N-Reactor spent nuclear fuel (SNF) stored at K-Basin to an interim storage facility require information about the oxidation behavior of the metallic uranium. Limited experiments have been performed on the oxidation reaction of SNF samples taken from an N-Reactor outer fuel element in various atmospheres. This report discusses studies on the oxidation behavior of SNF using two independent experimental systems: (1) a tube furnace with a flowing gas mixture of 2% oxygen/98% argon; and (2) a thermogravimetric system for dry air oxidation.

Abrefah, J.; Buchanan, H.C.; Gerry, W.M.; Gray, W.J.; Marschman, S.C.

1998-06-01T23:59:59.000Z

356

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]

comparable to National Uranium Resource Evaluation (NURE)comparable to National Uranium Resource Evaluation (NURE)

Samuel-Nakamura, Christine

2013-01-01T23:59:59.000Z

357

The uranium cylinder assay system for enrichment plant safeguards  

SciTech Connect (OSTI)

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

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

2010-01-01T23:59:59.000Z

358

In-line assay monitor for uranium hexafluoride  

DOE Patents [OSTI]

An in-line assay monitor for determining the content of uranium-235 in a uranium hexafluoride gas isotopic separation system is provided which removes the necessity of complete access to the operating parameters of the system for determining the uranium-235 content. The 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.

Wallace, S.A.

1980-03-21T23:59:59.000Z

359

In situ Microbial Community Control of the Stability of Bio-Reduced Uranium  

SciTech Connect (OSTI)

In aerobic aquifers typical of many Department of Energy (DOE) legacy waste sites, uranium is present in the oxidized U(VI) form which is soluble and thus mobile compared to U(IV). Previous work at the Old Rifle Uranium Mill Tailings Remedial Action (UMTRA) site demonstrated that biostimulation by acetate injection promoted growth of Geobacteraceae and stimulated the microbial reduction of U(VI) to less soluble U(IV) (1, 4). Despite the potential for oxidative dissolution of bio-reduced U(IV), field experiments at the Old Rifle site show that although the rate of U(VI) reduction decreases following the on-set of sulfate reduction, U(VI) reduction continues even following the cessation of acetate injection (1, 4). However, U(VI) reduction is reversible and the basis for the observed maintenance of U(VI) reduction post-stimulation is a critical but as yet unresolved issue for the application of biostimulation as a treatment technology. The continued U(VI) reduction and the maintenance of reduced U(IV) may result from many factors including U(VI) reduction by sulfate reducing bacteria (SRB), generation of H2S or FeS0.9 which serves as an oxygen sink, or the preferential sorption of U(VI) by microbial cells or biopolymers. The overall goal of the project is to develop an understanding of the mechanisms for the maintenance of bio-reduced uranium in an aerobic aquifer under field conditions following the cessation of electron donor addition.

Long, Phillip E.; McKinley, James P.; White, David C.

2006-06-01T23:59:59.000Z

360

Separation of uranium from nitric and hydrochloric acid solutions with extractant-coated magnetic microparticles.  

SciTech Connect (OSTI)

The magnetically assisted chemical separation (MACS) process utilizes selective magnetic microparticle composites to separate dissolved metals from solution. In this study, MACS particles were coated with neutral and acidic organophosphorus extractants,octyl(phenyl)-N,N-diisobutylcarbamoylmethyl phosphine oxide (CMPO), tributyl phosphate (TBP), trioctylphosphine oxide (TOPO), and bis(2-ethyl-hexyl)phosphoric acid (D{sub 2}EHPA or HDEHP) and were evaluated for the separation of uranyl ions from nitric- and hydrochloric-acid solutions. The results suggest that a synergistic interaction between the particle surface and solvent coating may explain why the particles display, in some cases, orders of magnitude of higher partitioning coefficients than are estimated from solvent-extraction measurements. Particles coated with TBP and those coated with a combination of TOPO and D{sub 2}EHPA displayed the most desirable characteristics for removing uranium from dilute acid environments typical of contaminated groundwater. Uranium separation from moderate to highly acidic waste streams typical of Department of Energy (DOE) nuclear wastes is best accomplished using particles coated with a combination of CMPO and TBP.

Kaminski, M. D.; Nunez, L.; Chemical Engineering

2000-01-01T23:59:59.000Z

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


361

The ultimate disposition of depleted uranium  

SciTech Connect (OSTI)

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

Not Available

1990-12-01T23:59:59.000Z

362

Energy balance for uranium recovery from seawater  

SciTech Connect (OSTI)

The energy return on investment (EROI) of an energy resource is the ratio of the energy it ultimately produces to the energy used to recover it. EROI is a key viability measure for a new recovery technology, particularly in its early stages of development when financial cost assessment would be premature or highly uncertain. This paper estimates the EROI of uranium recovery from seawater via a braid adsorbent technology. In this paper, the energy cost of obtaining uranium from seawater is assessed by breaking the production chain into three processes: adsorbent production, adsorbent deployment and mooring, and uranium elution and purification. Both direct and embodied energy inputs are considered. Direct energy is the energy used by the processes themselves, while embodied energy is used to fabricate their material, equipment or chemical inputs. If the uranium is used in a once-through fuel cycle, the braid adsorbent technology EROI ranges from 12 to 27, depending on still-uncertain performance and system design parameters. It is highly sensitive to the adsorbent capacity in grams of U captured per kg of adsorbent as well as to potential economies in chemical use. This compares to an EROI of ca. 300 for contemporary terrestrial mining. It is important to note that these figures only consider the mineral extraction step in the fuel cycle. At a reference performance level of 2.76 g U recovered per kg adsorbent immersed, the largest energy consumers are the chemicals used in adsorbent production (63%), anchor chain mooring system fabrication and operations (17%), and unit processes in the adsorbent production step (12%). (authors)

Schneider, E.; Lindner, H. [The University of Texas, 1 University Station C2200, Austin, TX 78712 (United States)

2013-07-01T23:59:59.000Z

363

Uranium enrichment export control guide: Gaseous diffusion  

SciTech Connect (OSTI)

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

Not Available

1989-09-01T23:59:59.000Z

364

Uranio impoverito: perché? (Depleted uranium: why?)  

E-Print Network [OSTI]

In this paper we develop a simple model of the penetration process of a long rod through an uniform target. Applying the momentum and energy conservation laws, we derive an analytical relation which shows how the penetration depth depends upon the density of the rod, given a fixed kinetic energy. This work was sparked off by the necessity of understanding the effectiveness of high density penetrators (e.g. depleted uranium penetrators) as anti-tank weapons.

Germano D'Abramo

2003-06-05T23:59:59.000Z

365

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

E-Print Network [OSTI]

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

366

Magnetic Exchange Coupling and Single-Molecule Magnetism in Uranium Complexes  

E-Print Network [OSTI]

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

Rinehart, Jeffrey Dennis

2010-01-01T23:59:59.000Z

367

E-Print Network 3.0 - active uranium americium Sample Search...  

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

<< < 1 2 3 4 5 > >> 21 geology and Ranger 1 open-pit uranium mine in Australia Summary: Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

368

E-Print Network 3.0 - alkaline-earth metal uranium Sample Search...  

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

In metamorphic rocks uranium and rare earth metals can form minerals. An example... Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

369

E-Print Network 3.0 - arlit uranium mines Sample Search Results  

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

Mathematics 5 geology and Ranger 1 open-pit uranium mine in Australia Summary: Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

370

E-Print Network 3.0 - area uranium plume Sample Search Results  

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

Sciences and Ecology 4 geology and Ranger 1 open-pit uranium mine in Australia Summary: Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

371

E-Print Network 3.0 - abandoned uranium mill Sample Search Results  

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

Sciences and Ecology 17 geology and Ranger 1 open-pit uranium mine in Australia Summary: Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

372

E-Print Network 3.0 - anaconda uranium mill Sample Search Results  

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

Sciences and Ecology 7 geology and Ranger 1 open-pit uranium mine in Australia Summary: Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

373

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

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

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

374

E-Print Network 3.0 - acute uranium intoxication Sample Search...  

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

Biology and Medicine 19 geology and Ranger 1 open-pit uranium mine in Australia Summary: Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

375

E-Print Network 3.0 - atomized uranium silicide Sample Search...  

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

Materials Science 11 geology and Ranger 1 open-pit uranium mine in Australia Summary: Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

376

E-Print Network 3.0 - abandoned uranium mines Sample Search Results  

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

Sciences and Ecology 15 geology and Ranger 1 open-pit uranium mine in Australia Summary: Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

377

E-Print Network 3.0 - ash doped uranium Sample Search Results  

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

Sciences and Ecology 2 geology and Ranger 1 open-pit uranium mine in Australia Summary: Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

378

E-Print Network 3.0 - adepleted uranium hexafluoride Sample Search...  

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

Mathematics 15 geology and Ranger 1 open-pit uranium mine in Australia Summary: Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

379

E-Print Network 3.0 - alloyed uranium sicral Sample Search Results  

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

Sciences and Ecology 33 geology and Ranger 1 open-pit uranium mine in Australia Summary: Uranium geology and mining Ranger 1 open-pit uranium mine in Australia Mikael Hk UHDSG...

380

The geochemistry of uranium in the Orca Basin  

E-Print Network [OSTI]

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

Weber, Frederick Fewell

1979-01-01T23:59:59.000Z

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


381

Tables des principaux minerais d'uranium et de thorium  

E-Print Network [OSTI]

233 Tables des principaux minerais d'uranium et de thorium Par B. SZILARD [Faculté des Sciences de minerais d'uranium et de thorium avec leurs données les plus importantes, telles que la com- position, la teneur en uranium et en thorium, la provenance et quelques indications générales. La liste ne prétend pas

Paris-Sud XI, Université de

382

Uncertainty clouds uranium enrichment corporation's plans  

SciTech Connect (OSTI)

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

Lane, E.

1993-03-24T23:59:59.000Z

383

Oxidation catalyst  

DOE Patents [OSTI]

The present invention generally relates to catalyst systems and methods for oxidation of carbon monoxide. The invention involves catalyst compositions which may be advantageously altered by, for example, modification of the catalyst surface to enhance catalyst performance. Catalyst systems of the present invention may be capable of performing the oxidation of carbon monoxide at relatively lower temperatures (e.g., 200 K and below) and at relatively higher reaction rates than known catalysts. Additionally, catalyst systems disclosed herein may be substantially lower in cost than current commercial catalysts. Such catalyst systems may be useful in, for example, catalytic converters, fuel cells, sensors, and the like.

Ceyer, Sylvia T. (Cambridge, MA); Lahr, David L. (Cambridge, MA)

2010-11-09T23:59:59.000Z

384

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

385

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

SciTech Connect (OSTI)

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.

none,

2013-07-01T23:59:59.000Z

386

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

E-Print Network [OSTI]

coordination chemistry is depleted uranium, a by-product innuclear reactors. Depleted uranium Figure 1-1. The periodic

Lam, Oanh Phi

2010-01-01T23:59:59.000Z

387

Dissolution of Uranium-Bearing Minerals and Mobilization of Uranium by Organic Ligands in a Biologically Reduced Sediment  

SciTech Connect (OSTI)

The stability and mobility of uranium (U) is a concern following its reductive precipitation or immobilization by techniques such as bioremediation at contaminated sites. In this study, the influences of complexing organic ligands such as citrate and ethylenediaminetetraacetate (EDTA) on the mobilization of U were investigated in both batch and column flow systems using a contaminated and bioreduced sediment. Results indicate that both reduced U(IV) and oxidized U(VI) in the sediment can be effectively mobilized with the addition of EDTA or citrate under anaerobic conditions. The dissolution and mobilization of U appear to be correlated to the dissolution of iron (Fe)- or aluminum (Al)-bearing minerals, with EDTA being more effective (with R2 0.89) than citrate (R2 <0.60) in dissolving these minerals. The column flow experiments confirm that U, Fe, and Al can be mobilized by these ligands under anoxic conditions, although the cumulative amounts of U removal constituted ~0.1% of total U present in this sediment following a limited period of leaching. This study concludes that the presence of complexing organic ligands may pose a long-term concern by slowly dissolving U-bearing minerals and mobilizing U even under a strict anaerobic environment.

Luo, Wensui [ORNL; Gu, Baohua [ORNL

2011-01-01T23:59:59.000Z

388

Uranium in Framboidal Pyrite from a Naturally Bioreduced Alluvial...  

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

in Framboidal Pyrite from a Naturally Bioreduced Alluvial Sediment . Uranium in Framboidal Pyrite from a Naturally Bioreduced Alluvial Sediment . Abstract: Samples of a naturally...

389

Microscopic Reactive Diffusion of Uranium in the Contaminated...  

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

States. Abstract: Microscopic and spectroscopic analysis of uranium-contaminated sediment cores beneath the BX waste tank farm at the US Department of Energy (DOE) Hanford...

390

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

National Nuclear Security Administration (NNSA)

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

391

Method of fabricating a uranium-bearing foil  

DOE Patents [OSTI]

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.

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

2012-04-24T23:59:59.000Z

392

Uranium Leasing Program Draft PEIS Public Comment Period Extended...  

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

Uranium Leasing Program Draft PEIS Public Comment Period Extended to May 31, 2013 Draft ULPEIS comment extension community notification041813 (3).pdf More Documents & Publications...

393

Uranium immobilization by sulfate-reducing biofilms grown on...  

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

immobilization by sulfate-reducing biofilms grown on hematite, dolomite, and calcite. Uranium immobilization by sulfate-reducing biofilms grown on hematite, dolomite, and calcite....

394

Electrochemical method of producing eutectic uranium alloy and apparatus  

DOE Patents [OSTI]

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.

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

1995-01-10T23:59:59.000Z

395

High grade uranium resources in the United States : an overview  

E-Print Network [OSTI]

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

Graves, Richard E.

1974-01-01T23:59:59.000Z

396

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)...

397

Basic characterization of highly enriched uranium by gamma spectrometry  

E-Print Network [OSTI]

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

Cong Tam Nguyen; Jozsef Zsigrai

2005-08-25T23:59:59.000Z

398

Basic characterization of highly enriched uranium by gamma spectrometry  

E-Print Network [OSTI]

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

Nguyen, C T

2006-01-01T23:59:59.000Z

399

Measurements of uranium in soils and small mammals  

SciTech Connect (OSTI)

The objective of this study was to evaluate the bioavailability of uranium to a single species of small mammal, Peromyscus maniculatus rufinus (Merriam), white-footed deer mouse, from two different source terms: a Los Alamos National Laboratory dynamic weapons testing site in north central New Mexico, where an estimated 70,000 kg of uranium have been expended over a 31-y period; and an inactive uranium mill tailings pile located in west central New Mexico near Grants, which received wastes over a 5-y period from the milling of 2.7 x 10/sup 9/ kg of uranium ore.

Miera, F.R. Jr.

1980-12-01T23:59:59.000Z

400

EIS-0472: Uranium Leasing Program, Mesa, Montrose, and San Miguel...  

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

Uranium Leasing Program, Mesa, Montrose, and San Miguel Counties, Colorado March 15, 2013 EIS-0472: DOE Notice of Availability of a Draft Programmatic Environmental Impact...

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


401

Uranium biokinetics in gavaged young adult female rats.  

E-Print Network [OSTI]

??Blood, liver, kidney, femur, and ovaries were assayed from female Wistar rats following oral administration of uranyl nitrate. Three uranium concentrations were studied for six… (more)

Keizer, Philip John

1986-01-01T23:59:59.000Z

402

Assessment of Controlling Processes for Field-Scale Uranium Reactive...  

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

at the 300A site. However, the model simulations also revealed that the groundwater chemistry was relatively stable during the uranium tracer experiment and therefore...

403

americium plutonium uranium: Topics by E-print Network  

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

a fascinating ele- ment. Last year, we learned that some com- pounds of plutonium superconduct at sur- prisingly Steinberger, Bernhard 110 Standard specification for uranium...

404

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

Energy Savers [EERE]

set forth in the 2012 Secretarial Determination and the Department's Excess Uranium Inventory Management Plan released in July 2013. Secretarial Determination 5-15-14.pdf More...

405

Collaboration and Communication: DOE and Navajo Nation Tour Uranium...  

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

site managers, along with Navajo Nation technical staff, visited five reclaimed uranium-mine sites on tribal lands to share expertise in the use of technical approaches...

406

Financial Assurance for In Situ Uranium Facilities (Texas)  

Broader source: Energy.gov [DOE]

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

407

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

SciTech Connect (OSTI)

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

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

1993-02-01T23:59:59.000Z

408

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

SciTech Connect (OSTI)

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

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

1993-02-01T23:59:59.000Z

409

Pyroprocessing of Oxidized Sodium-Bonded Fast Reactor Fuel -- an Experimental Study of Treatment Options for Degraded EBR-II Fuel  

SciTech Connect (OSTI)

An experimental study was conducted to assess pyrochemical treatment options for degraded EBR-II fuel. As oxidized material, the degraded fuel would need to be converted back to metal to enable electrorefining within an existing electrometallurgical treatment process. A lithium-based electrolytic reduction process was studied to assess the efficacy of converting oxide materials to metal with a particular focus on the impact of zirconium oxide and sodium oxide on this process. Bench-scale electrolytic reduction experiments were performed in LiCl-Li2O at 650 °C with combinations of manganese oxide (used as a surrogate for uranium oxide), zirconium oxide, and sodium oxide. The experimental study illustrated how zirconium oxide and sodium oxide present different challenges to a lithium-based electrolytic reduction system for conversion of select metal oxides to metal.

S. D. Herrmann; L. A. Wurth; N. J. Gese

2013-09-01T23:59:59.000Z

410

Corrosion Evaluation of RERTR Uranium Molybdenum Fuel  

SciTech Connect (OSTI)

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

A K Wertsching

2012-09-01T23:59:59.000Z

411

A novel hohlraum with ultrathin depleted-uranium-nitride coating layer for low hard x-ray emission and high radiation temperature  

E-Print Network [OSTI]

An ultra-thin layer of uranium nitrides (UN) has been coated on the inner surface of the depleted uranium hohlraum (DUH), which has been proved by our experiment can prevent the oxidization of Uranium (U) effectively. Comparative experiments between the novel depleted uranium hohlraum and pure golden (Au) hohlraum are implemented on Shenguang III prototype laser facility. Under the laser intensity of 6*10^14 W/cm2, we observe that, the hard x-ray (> 1.8 keV) fraction of this uranium hohlraum decreases by 61% and the peak intensity of total x-ray flux (0.1 keV ~ 5 keV) increases by 5%. Two dimensional radiation hydrodynamic code LARED are exploited to interpret the above observations. Our result for the first time indicates the advantage of the UN-coated DUH in generating the uniform x-ray field with a quasi Planckian spectrum and thus has important implications in optimizing the ignition hohlraum design.

Guo, Liang; Xing, Peifeng; Li, Sanwei; Yi, Taimin; Kuang, Longyu; Li, Zhichao; Li, Renguo; Wu, Zheqing; Jing, Longfei; Zhang, Wenhai; Zhan, Xiayu; Yang, Dong; Jiang, Bobi; Yang, Jiamin; Liu, Shenye; Jiang, Shaoen; Li, Yongsheng; Liu, Jie; Huo, Wenyi; Lan, Ke

2014-01-01T23:59:59.000Z

412

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

E-Print Network [OSTI]

the open-pit mining employed elsewhere in uranium landscape.as open-pit and underground uranium mining. Local residents,

Voyles, Traci Brynne

2010-01-01T23:59:59.000Z

413

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...

414

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

E-Print Network [OSTI]

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

Lopez, Michael Joseph

2013-01-01T23:59:59.000Z

415

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

E-Print Network [OSTI]

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

Andersen, Richard A.

2012-01-01T23:59:59.000Z

416

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

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

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...

417

E-Print Network 3.0 - aqueuous uranium complexes Sample Search...  

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

12;Breccia complex deposits: This is a type of uranium formations that occur near... Uranium geology and mining Ranger ... Source: Uppsala Universitet, Department of...

418

E-Print Network 3.0 - adsorbing uranium compounds Sample Search...  

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

compound, davidite-brannerite-absite type of uranium titanates and the euxenite... Uranium geology and mining Ranger 1 ... Source: Uppsala Universitet, Department of...

419

E-Print Network 3.0 - alloyed uranium transformation Sample Search...  

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

the sink term in the governing mass balance equation and the transformation from average uranium... Mathematical Geology, Vol. 33, No. 1, 2001 Modeling Uranium Transport in ......

420

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

E-Print Network [OSTI]

P.C. , 1981, Geology of the Peńa Blanca uranium deposits,uranium mineralizations in the Sierra Peńa Blanca district, Chihuahua, Mexico: Three genetic models: Economic Geology,

Dobson, P.

2009-01-01T23:59:59.000Z

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


421

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

DOE Patents [OSTI]

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.

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

1982-06-29T23:59:59.000Z

422

Geochemical, mineralogical and microbiological characteristics of sediment from a naturally reduced zone in a uranium-contaminated aquifer  

SciTech Connect (OSTI)

Localized zones or lenses of naturally reduced sediments have the potential to play a significant role in the fate and transport of redox-sensitive metals and metalloids in aquifers. To assess the mineralogy, microbiology, and redox processes that occur in these zones, we examined several cores from a region of naturally occurring reducing conditions in a uranium-contaminated aquifer (Rifle, CO). Sediment samples from a transect of cores ranging from oxic/suboxic Rifle aquifer sediment to naturally reduced sediment were analyzed for uranium and iron content, oxidation state, and mineralogy, reduced sulfur phases, and solid phase organic carbon content using a suite of analytical and spectroscopic techniques on bulk sediment and size fractions. Solid-phase uranium concentrations were higher in the naturally reduced zone, with a high proportion of the uranium present as reduced U(IV). The sediments were also elevated in reduced sulfur phases and Fe(II), indicating it is very likely that U(VI), Fe(III), and sulfate reduction occurred or is occurring in the sediment. The microbial community was assessed using lipid- and DNA-based techniques, and statistical redundancy analysis was performed to determine correlations between the microbial community and the geochemistry. Increased concentration of solid phase organic carbon and biomass in the naturally reduced sediment suggests that natural bioreduction is stimulated by a zone of increased organic carbon concentration associated with fine-grained material and lower permeability to groundwater flow. Characterization of the naturally bioreduced sediment provides an understanding of the natural processes that occur in the sediment under reducing conditions and how they may impact natural attenuation of radionuclides and other redox sensitive materials. Results also suggest the importance of recalcitrant organic carbon for maintaining reducing conditions and uranium immobilization.

Campbell, Kate M.; Kukkadapu, Ravi K.; Qafoku, Nikolla; Peacock, Aaron D.; Lesher, E.; Williams, Kenneth H.; Bargar, John R.; Wilkins, Michael J.; Figueroa, Linda A.; Ranville, James; Davis, James; Long, Philip E.

2012-05-23T23:59:59.000Z

423

Development of Novel Sorbents for Uranium Extraction from Seawater  

SciTech Connect (OSTI)

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

Lin, Wenbin; Taylor-Pashow, Kathryn

2014-01-08T23:59:59.000Z

424

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

DOE Patents [OSTI]

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.

Stinton, David P. (Knoxville, TN)

1983-01-01T23:59:59.000Z

425

Assessment of Waste Treatment Plant Lab C3V (LB-S1) Stack Sampling Probe Location for Compliance with ANSI/HPS N13.1-1999  

SciTech Connect (OSTI)

This report documents a series of tests used to assess the proposed air sampling location in the Hanford Tank Waste Treatment and Immobilization Plant (WTP) Lab C3V (LB-S1) exhaust stack with respect to the applicable criteria regarding the placement of an air sampling probe. Federal regulations require that an air sampling probe be located in the exhaust stack in accordance with the criteria of American National Standards Institute/Health Physics Society (ANSI/HPS) N13.1-1999, Sampling and Monitoring Releases of Airborne Radioactive Substances from the Stack and Ducts of Nuclear Facilities. These criteria address the capability of the sampling probe to extract a sample that represents the effluent stream.

Glissmeyer, John A.; Geeting, John GH

2013-02-01T23:59:59.000Z

426

Appendix IV. Risks Associated with Conventional Uranium Milling Introduction  

E-Print Network [OSTI]

by the addition of water/lixiviant is generally collected by air pollution control mechanisms, which return 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

427

Process for recovering niobium from uranium-niobium alloys  

DOE Patents [OSTI]

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.

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

1983-01-01T23:59:59.000Z

428

Nuclear power fleets and uranium resources recovered from phosphates  

SciTech Connect (OSTI)

Current light water reactors (LWR) burn fissile uranium, whereas some future reactors, as Sodium fast reactors (SFR) will be capable of recycling their own plutonium and already-extracted depleted uranium. This makes them a feasible solution for the sustainable development of nuclear energy. Nonetheless, a sufficient quantity of plutonium is needed to start up an SFR, with the plutonium already being produced in light water reactors. The availability of natural uranium therefore has a direct impact on the capacity of the reactors (both LWR and SFR) that we can build. It is therefore important to have an accurate estimate of the available uranium resources in order to plan for the world's future nuclear reactor fleet. This paper discusses the correspondence between the resources (uranium and plutonium) and the nuclear power demand. Sodium fast reactors will be built in line with the availability of plutonium, including fast breeders when necessary. Different assumptions on the global uranium resources are taken into consideration. The largely quoted estimate of 22 Mt of uranium recovered for phosphate rocks can be seriously downscaled. Based on our current knowledge of phosphate resources, 4 Mt of recoverable uranium already seems to be an upper bound value. The impact of the downscaled estimate on the deployment of a nuclear fleet is assessed accordingly. (authors)

Gabriel, S.; Baschwitz, A.; Mathonniere, G. [CEA, DEN/DANS/I-tese, F-91191 Gif-sur-Yvette (France)

2013-07-01T23:59:59.000Z

429

In-line assay monitor for uranium hexafluoride  

DOE Patents [OSTI]

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

Wallace, Steven A. (Knoxville, TN)

1981-01-01T23:59:59.000Z

430

Uranium and cesium diffusion in fuel cladding of electrogenerating channel  

SciTech Connect (OSTI)

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.

Vasil’ev, I. V., E-mail: fnti@mail.ru; Ivanov, A. S.; Churin, V. A. [National Research Center Kurchatov Institute (Russian Federation)

2014-12-15T23:59:59.000Z

431

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

SciTech Connect (OSTI)

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.

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

1981-04-01T23:59:59.000Z

432

Process for recovering niobium from uranium-niobium alloys  

DOE Patents [OSTI]

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.

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

1982-09-27T23:59:59.000Z

433

NUREG/CR-6911 Tests of Uranium (VI) Adsorption  

E-Print Network [OSTI]

NUREG/CR-6911 Tests of Uranium (VI) Adsorption Models in a Field Setting U.S. Geological Survey U/CR-6911 Tests of Uranium (VI) Adsorption Models in a Field Setting Manuscript Completed: August 2006 Date Published: August 2006 Prepared by G. P. Curtis, J. A. Davis Water Resources Division U.S. Geological Survey

434

Spectroscopic Evidence for Uranium Bearing Precipitates in Vadose Zone  

E-Print Network [OSTI]

Spectroscopic Evidence for Uranium Bearing Precipitates in Vadose Zone Sediments at the Hanford 300, Advanced Light Source, One Cyclotron Road, Berkeley, California 94720, United States Geological Survey Northwest Laboratory, Richland, Washington 99352 Uranium (U) solid-state speciation in vadose zone sediments

435

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 products sold (U.S. Department of 1Corresponding author: U.S. Geological Survey, California Water Science

436

Electron Microbeam Investigation of Uranium-Contaminated Soils from  

E-Print Network [OSTI]

Research Electron Microbeam Investigation of Uranium-Contaminated Soils from Oak Ridge, TN, USA J O Street, Baltimore, Maryland 21218, Department of Geological Sciences, Indiana University, 1001 East 10th Street, Bloomington, Indiana 47405 Two samples of uranium-contaminated soil from the Department of Energy

Zhu, Chen

437

Preserving Ultra-Pure Uranium-233  

SciTech Connect (OSTI)

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,

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

2011-10-01T23:59:59.000Z

438

Modeled atmospheric radon concentrations from uranium mines  

SciTech Connect (OSTI)

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.

Droppo, J.G.

1985-04-01T23:59:59.000Z

439

Production of Mo-99 using low-enriched uranium silicide  

SciTech Connect (OSTI)

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

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

1994-09-01T23:59:59.000Z

440

National uranium resource evaluation: Clifton Quadrangle, Arizona and New Mexico  

SciTech Connect (OSTI)

The Clifton Quadrangle, Arizona and New Mexico, was evaluated to identify environments and delineate areas favorable for uranium deposits. The evaluation used criteria formulated for the National Uranium Resource Evaluation program. Evidence for the evaluation was based on surface studies, hydrogeochemical and stream-sediment reconnaissance, and aerial radiometric surveys. The quadrangle encompasses parts of three physiographic provinces: the Colorado Plateau, the transition zone, and the Basin and Range. The one environment determined, during the present study, to be favorable for uranium deposits is the Whitewater Creek member of the Cooney tuff, which is favorable for magmatic-hydrothermal uranium deposits on the west side of the Bursum caldera. No other areas were favorable for uranium deposits in sandstone, limestone, volcanogenic, igneous, or metamorphic environments. The subsurface is unevaluated because of lack of information, as are areas where access is a constraint.

White, D L; Foster, M

1982-05-01T23:59:59.000Z

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


441

Active neutron multiplicity counting of bulk uranium  

SciTech Connect (OSTI)

This paper describes a new nondestructive assay technique being developed to assay bulk uranium containing kilogram quantities of {sup 235}U. The new technique uses neutron multiplicity analysis of data collected with a coincidence counter outfitted with AmLi neutron sources. We have calculated the expected neutron multiplicity count rate and assay precision for this technique and will report on its expected performance as a function of detector design characteristics, {sup 235 }U sample mass, AmLi source strength, and source-to-sample coupling. 11 refs., 2 figs., 2 tabs.

Ensslin, N.; Krick, M.S.; Langner, D.G.; Miller, M.C.

1991-01-01T23:59:59.000Z

442

Uranium Management and Policy | Department of Energy  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear SecurityTensile Strain Switched Ferromagnetism inS-4500II Field Emission SEM with EDAXUpdatedEnergyUranium Management

443

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:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"Click worksheet9,1,50022,3,,,,6,1,,781Title: Telephone:short version) Themonthly4 Oil(EIA)Uranium

444

SciTech Connect: enriched uranium  

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

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

445

U.S. Uranium Reserves Estimates  

Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelinesProved ReservesFeet)per Thousand28 198 18Biomass GasPropane,Major U.S. Uranium

446

U.S. Uranium Reserves Estimates  

Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelinesProved ReservesFeet)per Thousand28 198 18Biomass GasPropane,Major U.S. Uranium1. U.S.

447

U.S. Uranium Reserves Estimates  

Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelinesProved ReservesFeet)per Thousand28 198 18Biomass GasPropane,Major U.S. Uranium1.

448

Innovative Elution Processes for Recovering Uranium from Seawater  

SciTech Connect (OSTI)

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.

Wai, Chien; Tian, Guoxin; Janke, Christopher

2014-05-29T23:59:59.000Z

449

Decommissioning of U.S. uranium production facilities  

SciTech Connect (OSTI)

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.

Not Available

1995-02-01T23:59:59.000Z

450

Process for combined control of mercury and nitric oxide.  

SciTech Connect (OSTI)

Continuing concern about the effects of mercury in the environment may lead to requirements for the control of mercury emissions from coal-fired power plants. If such controls are mandated, the use of existing flue-gas cleanup systems, such as wet scrubbers currently employed for flue-gas desulfurization, would be desirable, Such scrubbers have been shown to be effective for capturing oxidized forms of mercury, but cannot capture the very insoluble elemental mercury (Hg{sup 0}) that can form a significant fraction of the total emissions. At Argonne National Laboratory, we have proposed and tested a concept for enhancing removal of Hg{sup 0}, as well as nitric oxide, through introduction of an oxidizing agent into the flue gas upstream of a scrubber, which readily absorbs the soluble reaction products. Recently, we developed a new method for introducing the oxidizing agent into the flue-gas stream that dramatically improved reactant utilization. The oxidizing agent employed was NOXSORB{trademark}, which is a commercial product containing chloric acid and sodium chlorate. When a dilute solution of this agent was introduced into a gas stream containing Hg{sup 0} and other typical flue-gas species at 300 F, we found that about 100% of the mercury was removed from the gas phase and recovered in process liquids. At the same time, approximately 80% of the nitric oxide was removed. The effect of sulfur dioxide on this process was also investigated and the results showed that it slightly decreased the amount of Hg{sup 0} oxidized while appearing to increase the removal of nitric oxide from the gas phase. We are currently testing the effects of variations in NOXSORB{trademark} concentration, sulfur dioxide concentration, nitric oxide concentration, and reaction time (residence time). Preliminary economic projections based on the results to date indicate that the chemical cost for nitric oxide oxidation could be less than $5,000/ton removed, while for Hg{sup 0} oxidation it would be about $20,000/lb removed.

Livengood, C. D.; Mendelsohn, M. H.

1999-11-03T23:59:59.000Z

451

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

DOE Patents [OSTI]

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.

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

1989-01-01T23:59:59.000Z

452

Defining Conditions for Maximizing Bioreduction of Uranium  

SciTech Connect (OSTI)

Correlations between modifying electron donor and acceptor accessibility, the in-situ microbial community, and bioreduction of Uranium at the FRC and UMTRA research sites indicated that significant modifications in the rate, amount and by inference the potential stability of immobilized Uranium are feasible in these environments. The in-situ microbial community at these sites was assessed with a combination of lipid and real-time molecular techniques providing quantitative insights of effects of electron donor and manipulations. Increased (9mM in 2003 vs 3mM 2002) donor amendment at the Old Rifle site resulted in the stimulation of anaerobic conditions downgradient of the injection gallery. Biomass within the test plot increased relative to the control well at 17 feet. Q-PCR specific for IRB/SRB showed increased copy numbers within the test plot and was the highest at the injection gallery. Q-PCR specific for Geobacter sp. showed increased copy numbers within the test plot but further downgradient from the injection gallery than the SRB/IRB. DNA and Lipid analysis confirm changes in the microbial community structure due to donor addition. See also the PNNL (Long) and UMASS (Anderson) posters for more information about this site.

David C. White; Aaron D. Peacock; Yun-Juan Chang; Roland Geyer; Philip E. Long; Jonathan D. Istok; Amanda N.; R. Todd Anderson; Dora Ogles

2004-03-17T23:59:59.000Z

453

RIB Production with Photofission of Uranium  

E-Print Network [OSTI]

The process of uranium photofission with electron beams of 20 div 50 MeV is considered in terms of the production of fission fragments. It is shown that in the interaction between an electron beam (25 MeV in energy and 20 mu A in intensity), produced by a compact accelerator of the microtron type, and a uranium target of about 40 g/cm^2 in thickness, an average of 1.5 cdot 10^11 fission events/second is generated. According to the calculations and test experiments, this corresponds to the yield of ^132 Sn and ^142 Xe isotopes of approximately 2 cdot 10^9/s. The results of experiments on the optimal design of the U-target are presented. Problems are discussed connected with the separation of isotopes and isobars for their furher acceleration up to energies of 5-18 MeV/n. The photofission reactions of a heavy nucleus are compared with other methods of RIB production of medium mass nuclei.

Oganessian, Yu T; Kliman, J; Maslov, O D; Starodub, G Ya; Belov, A G; Tretyakova, S P

2002-01-01T23:59:59.000Z

454

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

E-Print Network [OSTI]

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

Boyer, Edmond

455

Short Communication Bioreduction and precipitation of uranium in ionic liquid aqueous  

E-Print Network [OSTI]

with uranium from mining and milling operations, radioactive wastes, and from nuclear accidents is a majorShort Communication Bioreduction and precipitation of uranium in ionic liquid aqueous solution t s Uranium forms various complexes with ionic liquids. Uranium bioreduction was affected by the type

Ohta, Shigemi

456

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

E-Print Network [OSTI]

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

Zhang, Zhicheng

2009-01-01T23:59:59.000Z

457

Status Report and Proposal Concerning the Supply of Depleted Uranium Metal Bands for a Particle Detector  

E-Print Network [OSTI]

Status Report and Proposal Concerning the Supply of Depleted Uranium Metal Bands for a Particle Detector

1980-01-01T23:59:59.000Z

458

Final Scientific/Technical Report for Project entitled "Mechanism of Uranium Reduction by Shewanella oneidensis"  

SciTech Connect (OSTI)

Final Scientific/Technical Report for Project entitled "Mechanism of Uranium Reduction by Shewanella oneidensis"

DiChristina, Thomas J. [Georgia Tech

2013-04-30T23:59:59.000Z

459

E-Print Network 3.0 - arsenic manganese uranium Sample Search...  

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

IN-SITU LEACHIN-SITU RECOVERY (ISLISR) SITES Radiation Protection Division Office... .1 Uranium Geology......

460

THERMODYNAMIC MODEL FOR URANIUM DIOXIDE BASED NUCLEAR FUEL  

SciTech Connect (OSTI)

Many projects involving nuclear fuel rest on a quantitative understanding of the co-existing phases at various stages of burnup. Since the many fission products have considerably different abilities to chemically associate with oxygen, and the oxygen-to-metal molar ratio is slowly changing, the chemical potential of oxygen is a function of burnup. Concurrently, well-recognized small fractions of new phases such as inert gas, noble metals, zirconates, etc. also develop. To further complicate matters, the dominant UO2 fuel phase may be non-stoichiometric and most of the minor phases themselves have a variable composition dependent on temperature and possible contact with the coolant in the event of a sheathing breach. A thermodynamic fuel model to predict the phases in partially burned CANDU (CANada Deuterium Uranium) nuclear fuel containing many major fission products has been under development. The building blocks of the model are the standard Gibbs energies of formation of the many possible compounds expressed as a function of temperature. To these data are added mixing terms associated with the appearance of the component species in particular phases. In operational terms, the treatment rests on the ability to minimize the Gibbs energy in a multicomponent system, in our case using the algorithms developed by Eriksson. The model is capable of handling non-stoichiometry in the UO2 fluorite phase, dilute solution behaviour of significant solute oxides, noble metal inclusions, a second metal solid solution U(Pd-Rh-Ru)3, zirconate, molybdate, and uranate solutions as well as other minor solid phases, and volatile gaseous species.

Thompson, Dr. William T. [Royal Military College of Canada; Lewis, Dr. Brian J [Royal Military College of Canada; Corcoran, E. C. [Royal Military College of Canada; Kaye, Dr. Matthew H. [Royal Military College of Canada; White, S. J. [Royal Military College of Canada; Akbari, F. [Atomic Energy of Canada Limited, Chalk River Laboratories; Higgs, Jamie D. [Atomic Energy of Canada Limited, Point Lepreau; Thompson, D. M. [Praxair Inc.; Besmann, Theodore M [ORNL; Vogel, S. C. [Los Alamos National Laboratory (LANL)

2007-01-01T23:59:59.000Z

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


461

New insights into uranium (VI) sol-gel processing  

SciTech Connect (OSTI)

Nuclear Magnetic Resonance (NMR) investigations on the Oak Ridge National Laboratory process for sol-gel synthesis of microspherical nuclear fuel (UO{sub 2}), has been extremely useful in sorting out the chemical mechanism in the sol-gel steps. {sup 13}C, {sup 15}N, and {sup 1}H NMR studies on the HMTA gelation agent (Hexamethylene tetramine, C{sub 6}H{sub 12}N{sub 4}) has revealed near quantitative stability of this adamantane-like compound in the sol-gel process, contrary to its historical role as an ammonia source for gelation from the worldwide technical literature. {sup 17}O NMR of uranyl (UO{sub 2}{sup ++}) hydrolysis fragments produced in colloidal sols has revealed the selective formation of a uranyl trimer, ((UO{sub 2}){sub 3}({mu}{sub 3}-O)({mu}{sub 2}-OH){sub 3}){sup +}, induced by basic hydrolysis with the HMTA gelation agent. Spectroscopic results will be presented to illustrate that trimer condensation occurs during sol-gel processing leading to layered polyanionic hydrous uranium oxides in which HMTAH{sup +} is occluded as an intercalation'' cation. Subsequent sol-gel processing of microspheres by ammonia washing results in in-situ exchange and formation of a layered hydrous ammonium uranate with a proposed structural formula of (NH{sub 4}){sub 2} ((UO{sub 2}){sub 8} O{sub 4} (OH){sub 10}) {center dot} 8H{sub 2}O. This compound is the precursor to sintered UO{sub 2} ceramic fuel. 23 refs., 10 figs.

King, C.M.; Thompson, M.C.; Buchanan, B.R. (Westinghouse Savannah River Co., Aiken, SC (USA)); King, R.B. (Georgia Univ., Athens, GA (USA). Dept. of Chemistry); Garber, A.R. (South Carolina Univ., Columbia, SC (USA). Dept. of Chemistry)

1990-01-01T23:59:59.000Z

462

PWR core design, neutronics evaluation and fuel cycle analysis for thorium-uranium breeding recycle  

SciTech Connect (OSTI)

This paper was focused on core design, neutronics evaluation and fuel cycle analysis for Thorium-Uranium Breeding Recycle in current PWRs, without any major change to the fuel lattice and the core internals, but substituting the UOX pellet with Thorium-based pellet. The fuel cycle analysis indicates that Thorium-Uranium Breeding Recycle is technically feasible in current PWRs. A 4-loop, 193-assembly PWR core utilizing 17 x 17 fuel assemblies (FAs) was taken as the model core. Two mixed cores were investigated respectively loaded with mixed reactor grade Plutonium-Thorium (PuThOX) FAs and mixed reactor grade {sup 233}U-Thorium (U{sub 3}ThOX) FAs on the basis of reference full Uranium oxide (UOX) equilibrium-cycle core. The UOX/PuThOX mixed core consists of 121 UOX FAs and 72 PuThOX FAs. The reactor grade {sup 233}U extracted from burnt PuThOX fuel was used to fabrication of U{sub 3}ThOX for starting Thorium-. Uranium breeding recycle. In UOX/U{sub 3}ThOX mixed core, the well designed U{sub 3}ThOX FAs with 1.94 w/o fissile uranium (mainly {sup 233}U) were located on the periphery of core as a blanket region. U{sub 3}ThOX FAs remained in-core for 6 cycles with the discharged burnup achieving 28 GWD/tHM. Compared with initially loading, the fissile material inventory in U{sub 3}ThOX fuel has increased by 7% via 1-year cooling after discharge. 157 UOX fuel assemblies were located in the inner of UOX/U{sub 3}ThOX mixed core refueling with 64 FAs at each cycle. The designed UOX/PuThOX and UOX/U{sub 3}ThOX mixed core satisfied related nuclear design criteria. The full core performance analyses have shown that mixed core with PuThOX loading has similar impacts as MOX on several neutronic characteristic parameters, such as reduced differential boron worth, higher critical boron concentration, more negative moderator temperature coefficient, reduced control rod worth, reduced shutdown margin, etc.; while mixed core with U{sub 3}ThOX loading on the periphery of core has no visible impacts on neutronic characteristics compared with reference full UOX core. The fuel cycle analysis has shown that {sup 233}U mono-recycling with U{sub 3}ThOX fuel could save 13% of natural uranium resource compared with UOX once through fuel cycle, slightly more than that of Plutonium single-recycling with MOX fuel. If {sup 233}U multi-recycling with U{sub 3}ThOX fuel is implemented, more natural uranium resource would be saved. (authors)

Bi, G.; Liu, C.; Si, S. [Shanghai Nuclear Engineering Research and Design Inst., No. 29, Hongcao Road, Shanghai, 200233 (China)

2012-07-01T23:59:59.000Z

463

Some effects of data base variations on numerical simulations of uranium migration  

SciTech Connect (OSTI)

Numerical simulations of migration of chemicals in the geosphere depend on knowledge of identities of chemical species and on values of chemical equilibrium constants supplied to the simulators. In this work, some effects of variability in assumed speciation and in equilibrium constants were examined, using migration of uranium as an example. Various simulations were done of uranium migration in systems with varying oxidation potential, pH, and mator component content. A simulation including formation of aqueous species UO/sub 2//sup 2 +/, UO/sub 2/CO/sub 3//sup 0/, UO/sub 2/(CO/sub 3/)/sub 2//sup 2 -/, UO/sub 2/(CO/sub 3/)/sub 3//sup 4 -/, (UO/sub 2/)/sub 2/CO/sub 3/(OH)/sub 3//sup -/, UO/sub 2//sup +/, U(OH)/sub 4//sup 0/, and U(OH)/sub 5//sup -/ is compared to simulation excluding formation of UO/sub 2//sup +/ and U(OH)/sub 5//sup -/. These simulations relied on older data bases, and they are compared to a further simulation using recently published data on formation of U(OH)/sub 4//sup 0/, (UO/sub 2/)/sub 2/CO/sub 3/(OH)/sub 3//sup -/, UO/sub 2/(CO/sub 3/)/sub 5//sup 5 -/, and U(CO/sub 3/)/sub 5//sup 6 -/. Significant differences in dissolved uranium concentrations are noted among the simulations. Differences are noted also in precipitation of two solids, USiO/sub 4/(c) (coffinite) and CaUO/sub 4/(c) (calcium uranate), although the solubility products of the solids were not varied in the simulations. 18 refs., 9 figs., 2 tabs.

Carnahan, C.L.

1987-12-01T23:59:59.000Z

464

Project Profile: High Performance Reduction/Oxidation Metal Oxides...  

Office of Environmental Management (EM)

High Performance ReductionOxidation Metal Oxides for Thermochemical Energy Storage Project Profile: High Performance ReductionOxidation Metal Oxides for Thermochemical Energy...

465

Occupational exposures to uranium: processes, hazards, and regulations  

SciTech Connect (OSTI)

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

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

1981-04-01T23:59:59.000Z

466

Trivalent metallocene chemistry of some uranium, titanium, and zirconium complexes  

SciTech Connect (OSTI)

Dicyclopentadienyluranium halide dimers have been prepared and their solution behavior examined. These molecules exist as dimers in solution, and the halide ligands undergo rapid site exchange on the NMR timescale above 50 C. Analogous dicyclopentadienyluranium hydroxide dimers have also been prepared; they oxidatively eliminate hydrogen to give the corresponding oxide dimers. Mechanism of this reaction is consistent with {alpha}migration of one of the hydroxide hydrogen atoms to a uranium center followed by elimination of hydrogen. Ground state of [(Me{sub 3}Si){sub 2}C{sub 5}H{sub 3}]{sub 3}M M = Nd, U and their base adducts has been examined by variable temperature magnetic susceptibility and EPR spectroscopy. The ground state is found to be {sup 4}I{sub 9/2} with a crystal field state consisting largely of J{sub z} = 1/2 lowest, in agreement with previous studies on tris-cyclopentadienylneodymium complexes. The zirconium metallocene Cp{sub 3}Zr has been prepared, characterized crystallographically, and its reactivity studied. Its chemical behavior is controlled by presence of an electron in the non-bonding, d{sub z}2 orbital which prevents formation of base adducts Of Cp{sub 3}Zr, but allows Cp{sub 3}Zr to abstract atoms from other molecules. Electonic and EPR spectra of Cp*{sub 2}TiX complexes, where Cp* is Me{sub 5}C{sub 5} and X is a monodentate, anionic ligand such as halide, have been studied. A {pi}-bonding spectrochemical series is developed, and trends in {pi}-bonding ability are found similar to those in other inorganic complexes. The {beta}-agostic interactions in Cp*{sub 2}TiN(Me)Ph have been examined using variable temperature EPR spectroscopy, and the enthalpy/entropy of the interaction determined. In Cp*{sub 2}TiEt, enthalpy of the {beta}-agostic interaction is {minus}1.9 kcal/mol. The titanocene anion, Cp*{sub 2}TiLi(TMEDA) (TMEDA is N,N,N`,N`-tetramethylethylenediamine), has been prepared and its structure determined.

Lukens, W.W. Jr.

1995-05-01T23:59:59.000Z