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Sample records for uranium hexafluoride liquid

  1. Uranium hexafluoride liquid thermal expansion, elusive eutectic with hydrogen fluoride, and very first production using chlorine trifluoride

    Energy Technology Data Exchange (ETDEWEB)

    Rutledge, G.P. [Central Environmental, Inc., Anchorage, AK (United States)

    1991-12-31

    Three unusual incidents and case histories involving uranium hexafluoride in the enrichment facilities of the USA in the late 1940`s and early 1950`s are presented. The history of the measurements of the thermal expansion of liquids containing fluorine atoms within the molecule is reviewed with special emphasis upon uranium hexafluoride. A comparison is made between fluorinated esters, fluorocarbons, and uranium hexafluoride. The quantitative relationship between the thermal expansion coefficient, a, of liquids and the critical temperature, T{sub c} is presented. Uranium hexafluoride has an a that is very high in a temperature range that is used by laboratory and production workers - much higher than any other liquid measured. This physical property of UF{sub 6} has resulted in accidents involving filling the UF{sub 6} containers too full and then heating with a resulting rupture of the container. Such an incident at a uranium gaseous diffusion plant is presented. Production workers seldom {open_quotes}see{close_quotes} uranium hexafluoride. The movement of UF{sub 6} from one container to another is usually trailed by weight, not sight. Even laboratory scientists seldom {open_quotes}see{close_quotes} solid or liquid UF{sub 6} and this can be a problem at times. This inability to {open_quotes}see{close_quotes} the UF{sub 6}-HF mixtures in the 61.2{degrees}C to 101{degrees}C temperature range caused a delay in the understanding of the phase diagram of UF{sub 6}-HF which has a liquid - liquid immiscible region that made the eutectic composition somewhat elusive. Transparent fluorothene tubes solved the problem both for the UF{sub 6}-HF phase diagram as well as the UF{sub 6}-HF-CIF{sub 3} phase diagram with a miscibility gap starting at 53{degrees}C. The historical background leading to the first use of CIF{sub 3} to produce UF{sub 6} in both the laboratory and plant at K-25 is presented.

  2. Uranium hexafluoride purification

    International Nuclear Information System (INIS)

    Araujo, Eneas F. de

    1986-01-01

    Uranium hexafluoride might contain a large amount of impurities after manufacturing or handling. Three usual methods of purification of uranium hexafluoride were presented: selective sorption, sublimation, and distillation. Since uranium hexafluoride usually is contaminated with hydrogen fluoride, a theoretical study of the phase equilibrium properties was performed for the binary system UF 6 -HF. A large deviation from the ideal solution behaviour was observed. A purification unity based on a constant reflux batch distillation process was developed. A procedure was established in order to design the re boiler, condenser and packed columns for the UF 6 -HF mixture separation. A bench scale facility for fractional distillation of uranium hexafluoride was described. Basic operations for that facility and results extracted from several batches were discussed. (author)

  3. Reduction of uranium hexafluoride to uranium tetrafluoride

    International Nuclear Information System (INIS)

    Chang, I.S.; Do, J.B.; Choi, Y.D.; Park, M.H.; Yun, H.H.; Kim, E.H.; Kim, Y.W.

    1982-01-01

    The single step continuous reduction of uranium hexafluoride (UF 6 ) to uranium tetrafluoride (UF 4 ) has been investigated. Heat required to initiate and maintain the reaction in the reactor is supplied by the highly exothermic reaction of hydrogen with a small amount of elemental fluorine which is added to the uranium hexafluoride stream. When gases uranium hexafluoride and hydrogen react in a vertical monel pipe reactor, the green product, UF 4 has 2.5g/cc in bulk density and is partly contaminated by incomplete reduction products (UF 5 ,U 2 F 9 ) and the corrosion product, presumably, of monel pipe of the reactor itself, but its assay (93% of UF 4 ) is acceptable for the preparation of uranium metal with magnesium metal. Remaining problems are the handling of uranium hexafluoride, which is easily clogging the flowmeter and gas feeding lines because of extreme sensitivity toward moisture, and a development of gas nozzel for free flow of uranium hexafluoride gas. (Author)

  4. Uranium hexafluoride handling

    International Nuclear Information System (INIS)

    1991-01-01

    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 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

  5. Collect method of uranium hexafluoride

    International Nuclear Information System (INIS)

    Moura, S.C.; Bustillos, O.W.V.

    1991-01-01

    A collect method of uranium hexafluoride was designed, constructed and assembled in Analytical Laboratory from Instituto de Energia Atomica, Sao Paulo, Brazil. This method of collect is main for quality control of uranium hexafluoride. (author)

  6. Uranium hexafluoride handling. Proceedings

    Energy Technology Data Exchange (ETDEWEB)

    1991-12-31

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

  7. Standard practice for bulk sampling of liquid uranium hexafluoride

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2001-01-01

    1.1 This practice covers methods for withdrawing representative samples of liquid uranium hexafluoride (UF6) from bulk quantities of the material. Such samples are used for determining compliance with the applicable commercial specification, for example Specification C787 and Specification C996. 1.2 It is assumed that the bulk liquid UF6 being sampled comprises a single quality and quantity of material. This practice does not address any special additional arrangements that might be required for taking proportional or composite samples, or when the sampled bulk material is being added to UF6 residues already in a container (“heels recycle”). 1.3 The number of samples to be taken, their nominal sample weight, and their disposition shall be agreed upon between the parties. 1.4 The scope of this practice does not include provisions for preventing criticality incidents. 1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of th...

  8. Synthesis of graphite intercalation compound of group VI metals and uranium hexafluorides

    International Nuclear Information System (INIS)

    Fukui, Toshihiro; Hagiwara, Rika; Ema, Keiko; Ito, Yasuhiko

    1993-01-01

    Systematic investigations were made on the synthesis of graphite intercalation compounds of group VI transition metals (W and Mo) and uranium hexafluorides. The reactions were performed by interacting liquid or gaseous metal hexafluorides with or without elemental fluorine at ambient temperature. The degree of intercalation of these metal fluorides depends on the formation enthalpy of fluorometallate anion from the original metal hexafluoride, as has been found for other intercalation reactions of metal fluorides. (author)

  9. Uranium hexafluoride purification; Purificacao de hexafluoreto de uranio

    Energy Technology Data Exchange (ETDEWEB)

    Araujo, Eneas F. de

    1986-07-01

    Uranium hexafluoride might contain a large amount of impurities after manufacturing or handling. Three usual methods of purification of uranium hexafluoride were presented: selective sorption, sublimation, and distillation. Since uranium hexafluoride usually is contaminated with hydrogen fluoride, a theoretical study of the phase equilibrium properties was performed for the binary system UF{sub 6}-HF. A large deviation from the ideal solution behaviour was observed. A purification unity based on a constant reflux batch distillation process was developed. A procedure was established in order to design the re boiler, condenser and packed columns for the UF{sub 6}-HF mixture separation. A bench scale facility for fractional distillation of uranium hexafluoride was described. Basic operations for that facility and results extracted from several batches were discussed. (author)

  10. Obtention of uranium tetrafluoride from effluents generated in the hexafluoride conversion process

    International Nuclear Information System (INIS)

    Silva Neto, J.B.; Urano de Carvalho, E.F.; Durazzo, M.; Riella, H.G.

    2009-01-01

    Full text: The uranium silicide (U3Si2) fuel is produced from uranium hexafluoride (UF6) as the primary raw material. The uranium tetrafluoride (UF4) and metallic uranium are the two subsequent steps. There are two conventional routes for UF4 production: the first one reduces the uranium from the UF6 hydrolysis solution by adding stannous chloride (SnCl2). The second one is based on the hydrofluorination of solid uranium dioxide (UO2) produced from the ammonium uranyl carbonate (AUC). This work introduces a third route, a dry way route which utilizes the recovering of uranium from liquid effluents generated in the uranium hexafluoride reconversion process adopted at IPEN/CNEN-SP. Working in the liquid phase, this route comprises the recovery of ammonium fluoride by NH4HF2 precipitation. The crystallized bifluoride is added to the solid UO2 to get UF4, which returns to the metallic uranium production process and, finally, to the U3Si2 powder production. The UF4 produced by this new route was chemically and physically characterized and will be able to be used as raw material for metallic uranium production by magnesiothermic reduction. (author)

  11. Process for producing uranium oxide rich compositions from uranium hexafluoride

    International Nuclear Information System (INIS)

    DeHollander, W.R.; Fenimore, C.P.

    1978-01-01

    Conversion of gaseous uranium hexafluoride to a uranium dioxide rich composition in the presence of an active flame in a reactor defining a reaction zone is achieved by separately introducing a first gaseous reactant comprising a mixture of uranium hexafluoride and a reducing carrier gas, and a second gaseous reactant comprising an oxygen-containing gas. The reactants are separated by a shielding gas as they are introduced to the reaction zone. The shielding gas temporarily separates the gaseous reactants and temporarily prevents substantial mixing and reacting of the gaseous reactants. The flame occurring in the reaction zone is maintained away from contact with the inlet introducing the mixture to the reaction zone. After suitable treatment, the uranium dioxide rich composition is capable of being fabricated into bodies of desired configuration for loading into nuclear fuel rods. Alternatively, an oxygen-containing gas as a third gaseous reactant is introduced when the uranium hexafluoride conversion to the uranium dioxide rich composition is substantially complete. This results in oxidizing the uranium dioxide rich composition to a higher oxide of uranium with conversion of any residual reducing gas to its oxidized form

  12. Model of the coercion uranium hexafluoride on a human body

    International Nuclear Information System (INIS)

    Babenko, S.P.

    2007-01-01

    A method for calculating certain quantities characterizing the effect of uranium hexafluoride (UF 6 ) on the human body under industrial conditions in uranium enrichment plants is described. It is assumed that the effect is determined by uranium and fluorine inhaled together with the products of hydrolysis of uranium hexafluoride. The proposed complex model consists of three models, the first of which describes the contamination of the industrial environment and the second and third describe inhalation and percutaneous intake. A relation is obtained between uranium and fluorine intake and the uranium hexafluoride concentration in air at the moment the compound is discharged [ru

  13. Sequoyah Uranium Hexafluoride Plant (Docket No. 40-8027): Final environmental statement

    International Nuclear Information System (INIS)

    1975-02-01

    The proposed action is the continuation of Source Material License SUB-1010 issued to Kerr-McGee Nuclear Corporation authorizing the operation of a uranium hexafluoride manufacturing facility located in Sequoyah County, Oklahoma, close to the confluence of the Illinois and Arkansas Rivers. The plant produces high purity uranium hexafluoride using uranium concentrates (yellowcake) as the starting material. It is currently designed to produce 5000 tons of uranium per year as uranium hexafluoride and has been in operation since February 1970 without significant environmental incident or discernible offsite effect. The manufacturing process being used includes wet chemical purification to convert yellowcake to pure uranium trioxide followed by dry chemical reduction, hydrofluorination, and fluorination technique to produce uranium hexafluoride. 8 figs, 12 tabs

  14. Dry uranium tetrafluoride process preparation using the uranium hexafluoride reconversion process effluents

    International Nuclear Information System (INIS)

    Silva Neto, Joao Batista da

    2008-01-01

    It is a well known fact that the use of uranium tetrafluoride allows flexibility in the production of uranium suicide and uranium oxide fuel. To its obtention there are two conventional routes, the one which reduces uranium from the UF 6 hydrolysis solution with stannous chloride, and the hydro fluorination of a solid uranium dioxide. In this work we are introducing a third and a dry way route, mainly utilized to the recovery of uranium from the liquid effluents generated in the uranium hexafluoride reconversion process, at IPEN/CNEN-SP. Working in the liquid phase, this route comprises the recuperation of ammonium fluoride by NH 4 HF 2 precipitation. Working with the solid residues, the crystallized bifluoride is added to the solid UO 2 , which comes from the U mini plates recovery, also to its conversion in a solid state reaction, to obtain UF 4 . That returns to the process of metallic uranium production unity to the U 3 Si 2 obtention. This fuel is considered in IPEN CNEN/SP as the high density fuel phase for IEA-R1m reactor, which will replace the former low density U 3 Si 2 -Al fuel. (author)

  15. 49 CFR 173.420 - Uranium hexafluoride (fissile, fissile excepted and non-fissile).

    Science.gov (United States)

    2010-10-01

    ... 49 Transportation 2 2010-10-01 2010-10-01 false Uranium hexafluoride (fissile, fissile excepted....420 Uranium hexafluoride (fissile, fissile excepted and non-fissile). (a) In addition to any other... non-fissile uranium hexafluoride must be offered for transportation as follows: (1) Before initial...

  16. Uranium hexafluoride. Bromine spectrophotometric determination

    International Nuclear Information System (INIS)

    Anon.

    Bromine determination in hydrolized uranium hexafluoride by reduction of bromates by ferrous sulfate, oxidation of bromides by potassium permanganate to give bromine which is extracted into carbon tetrachloride and transformed in eosine for spectrophotometry at 510 nm. The method is suitable for determining 5 to 150 ppm with respect to uranium [fr

  17. Decommissioning of an uranium hexafluoride pilot plant

    International Nuclear Information System (INIS)

    Santos, Ivan; Abrao, Alcidio; Carvalho, Fatima M.S.; Ayoub, Jamil M.S.

    2009-01-01

    The Institute of Nuclear and Energetic Researches has completed fifty years of operation, belongs to the National Commission for Nuclear Energy, it is situated inside the city of Sao Paulo. The IPEN-CNEN/SP is a Brazilian reference in the nuclear fuel cycle, researches in this field began in 1970, having dominance in the cycle steps from Yellow Cake to Uranium Hexafluoride technology. The plant of Uranium Hexafluoride produced 35 metric tonnes of this gas by year, had been closed in 1992, due to domain and total transference of know-how for industrial scale, demand of new facilities for the improvement of recent researches projects. The Institute initiates decommissioning in 2002. Then, the Uranium Hexafluoride pilot plant, no doubt the most important unit of the fuel cycle installed at IPEN-CNEN/SP, beginning decommissioning and dismantlement (D and D) in 2005. Such D and D strategies, planning, assessment and execution are described, presented and evaluated in this paper. (author)

  18. Method for separation of uranium hexafluoride by specially activated carbons

    International Nuclear Information System (INIS)

    Bannasch, W.

    1976-01-01

    The present invention deals with the separation of urainium hexafluoride from gas streams on special activated carbon which can be released during an accident in nuclear plants. Those plants are concerned here in which as a rule uranium hexafluoride is handled in liquid aggregate state. The patent claims deal with the adsorption of UF 6 from gas mixtures in the temperature region of 70-200 0 C and the application of UF 6 adsorbing activated carbon of a certain grain based on petroleum and/or weight % and with a asch content of 4 to 6 weigt % and with a benzol yield of 50-60g benzene /100g activated carbon. (GG) [de

  19. Purification process of uranium hexafluoride containing traces of plutonium fluoride and/or neptunium fluoride

    International Nuclear Information System (INIS)

    Aubert, J.; Bethuel, L.; Carles, M.

    1983-01-01

    In this process impure uranium hexafluoride is contacted with a metallic fluoride chosen in the group containing lead fluoride PbF 2 , uranium fluorides UFsub(4+x) (0 3 at a temperature such as plutonium and/or neptunium are reduced and pure uranium hexafluoride is recovered. Application is made to uranium hexafluoride purification in spent fuel reprocessing [fr

  20. Analytical standards for accountability of uranium hexafluoride - 1972

    International Nuclear Information System (INIS)

    Anon.

    1976-01-01

    An analytical standard for the accountability of uranium hexafluoride is presented that includes procedures for subsampling, determination of uranium, determination of metallic impurities and isotopic analysis by gas and thermal ionization mass spectrometry

  1. Depleted Uranium Hexafluoride Management Program. The technology assessment report for the long-term management of depleted uranium hexafluoride. Volume 2

    International Nuclear Information System (INIS)

    Zoller, J.N.; Rosen, R.S.; Holliday, M.A.

    1995-01-01

    With the publication of a Request for Recommendations and Advance Notice of Intent in the November 10, 1994 Federal Register, the Department of Energy initiated a program to assess alternative strategies for the long-term management or use of depleted uranium hexafluoride. This Request was made to help ensure that, by seeking as many recommendations as possible, Department management considers reasonable options in the long-range management strategy. The Depleted Uranium Hexafluoride Management Program consists of three major program elements: Engineering Analysis, Cost Analysis, and an Environmental Impact Statement. This Technology Assessment Report is the first part of the Engineering Analysis Project, and assesses recommendations from interested persons, industry, and Government agencies for potential uses for the depleted uranium hexafluoride stored at the gaseous diffusion plants in Paducah, Kentucky, and Portsmouth, Ohio, and at the Oak Ridge Reservation in Tennessee. Technologies that could facilitate the long-term management of this material are also assessed. The purpose of the Technology Assessment Report is to present the results of the evaluation of these recommendations. Department management will decide which recommendations will receive further study and evaluation

  2. Depleted Uranium Hexafluoride Management Program. The technology assessment report for the long-term management of depleted uranium hexafluoride. Volume 2

    Energy Technology Data Exchange (ETDEWEB)

    Zoller, J.N.; Rosen, R.S.; Holliday, M.A. [and others

    1995-06-30

    With the publication of a Request for Recommendations and Advance Notice of Intent in the November 10, 1994 Federal Register, the Department of Energy initiated a program to assess alternative strategies for the long-term management or use of depleted uranium hexafluoride. This Request was made to help ensure that, by seeking as many recommendations as possible, Department management considers reasonable options in the long-range management strategy. The Depleted Uranium Hexafluoride Management Program consists of three major program elements: Engineering Analysis, Cost Analysis, and an Environmental Impact Statement. This Technology Assessment Report is the first part of the Engineering Analysis Project, and assesses recommendations from interested persons, industry, and Government agencies for potential uses for the depleted uranium hexafluoride stored at the gaseous diffusion plants in Paducah, Kentucky, and Portsmouth, Ohio, and at the Oak Ridge Reservation in Tennessee. Technologies that could facilitate the long-term management of this material are also assessed. The purpose of the Technology Assessment Report is to present the results of the evaluation of these recommendations. Department management will decide which recommendations will receive further study and evaluation.

  3. CFD-simulation of uranium hexafluoride during phase change

    International Nuclear Information System (INIS)

    Pakarinen, Tomi

    2014-01-01

    A model for simulating the behavior of uranium hexafluoride during melting and solidification cycles has been developed. First goal was to create a user-defined material of uranium hexafluoride for commercial computational fluid dynamics software (FLUENT). The results of the thermo physical properties are presented in this paper. The material properties were used to create a model that is able to simulate melting, solidification, evaporation and condensation. The model was used to obtain knowledge of UF 6 s behaviour when melting and solidifying the matter in a two-dimensional cylinder. The results were compared to the results of an analytical solution. The calculation results are consistent with the simulation. (authors)

  4. Depleted Uranium Hexafluoride Management Program. The technology assessment report for the long-term management of depleted uranium hexafluoride. Volume 1

    Energy Technology Data Exchange (ETDEWEB)

    Zoller, J.N.; Rosen, R.S.; Holliday, M.A. [and others

    1995-06-30

    With the publication of a Request for Recommendations and Advance Notice of Intent in the November 10, 1994 Federal Register, the Department of Energy initiated a program to assess alternative strategies for the long-term management or use of depleted uranium hexafluoride. This Request was made to help ensure that, by seeking as many recommendations as possible, Department management considers reasonable options in the long-range management strategy. The Depleted Uranium Hexafluoride Management Program consists of three major program elements: Engineering Analysis, Cost Analysis, and an Environmental Impact Statement. This Technology Assessment Report is the first part of the Engineering Analysis Project, and assesses recommendations from interested persons, industry, and Government agencies for potential uses for the depleted uranium hexafluoride stored at the gaseous diffusion plants in Paducah, Kentucky, and Portsmouth, Ohio, and at the Oak Ridge Reservation in Tennessee. Technologies that could facilitate the long-term management of this material are also assessed. The purpose of the Technology Assessment Report is to present the results of the evaluation of these recommendations. Department management will decide which recommendations will receive further study and evaluation. These Appendices contain the Federal Register Notice, comments on evaluation factors, independent technical reviewers resumes, independent technical reviewers manual, and technology information packages.

  5. Depleted Uranium Hexafluoride Management Program. The technology assessment report for the long-term management of depleted uranium hexafluoride. Volume 1

    International Nuclear Information System (INIS)

    Zoller, J.N.; Rosen, R.S.; Holliday, M.A.

    1995-01-01

    With the publication of a Request for Recommendations and Advance Notice of Intent in the November 10, 1994 Federal Register, the Department of Energy initiated a program to assess alternative strategies for the long-term management or use of depleted uranium hexafluoride. This Request was made to help ensure that, by seeking as many recommendations as possible, Department management considers reasonable options in the long-range management strategy. The Depleted Uranium Hexafluoride Management Program consists of three major program elements: Engineering Analysis, Cost Analysis, and an Environmental Impact Statement. This Technology Assessment Report is the first part of the Engineering Analysis Project, and assesses recommendations from interested persons, industry, and Government agencies for potential uses for the depleted uranium hexafluoride stored at the gaseous diffusion plants in Paducah, Kentucky, and Portsmouth, Ohio, and at the Oak Ridge Reservation in Tennessee. Technologies that could facilitate the long-term management of this material are also assessed. The purpose of the Technology Assessment Report is to present the results of the evaluation of these recommendations. Department management will decide which recommendations will receive further study and evaluation. These Appendices contain the Federal Register Notice, comments on evaluation factors, independent technical reviewers resumes, independent technical reviewers manual, and technology information packages

  6. Study of reactions for the production of uranium titrafluoride and uranium hexafluoride

    International Nuclear Information System (INIS)

    Guzella, M.F.R.

    1985-01-01

    The main production processes of uranium hexafluoride in pilot plants and industrial facilities are described. The known reactions confirmed in laboratory experiments that lead to Uf 6 or other intermediate fluorides are discussed. For the purpose of determining a thermodinamically feasible reaction involving the sulfur hexafluoride as fluorinating agent, a mock-up facility was designed and constructed as a part of the R and D work planned at the CDTN (Nuclebras Center for Nuclear Technology Development). IN the uranium tatrafluoride synthesis employing U 3 O 8 and SF 6 several experimental parameters are studied. The reaction time, gasflow, temperature and stoechiometic relations among reagents are described in detail. (Author) [pt

  7. Depleted uranium hexafluoride: Waste or resource?

    International Nuclear Information System (INIS)

    Schwertz, N.; Zoller, J.; Rosen, R.; Patton, S.; Bradley, C.; Murray, A.

    1995-07-01

    The US Department of Energy is evaluating technologies for the storage, disposal, or re-use of depleted uranium hexafluoride (UF 6 ). This paper discusses the following options, and provides a technology assessment for each one: (1) conversion to UO 2 for use as mixed oxide duel, (2) conversion to UO 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 3 O 8 as an option for long-term storage is discussed

  8. Reaction between uranium hexafluoride and trimethylsilylhalides

    Energy Technology Data Exchange (ETDEWEB)

    Brown, D; Berry, J A [UKAEA Atomic Energy Research Establishment, Harwell. Chemistry Div.; Holloway, J H; Staunton, G M [Leicester Univ. (UK). Dept. of Chemistry

    1938-07-01

    Reactions involving 1.1:1 molar ratios of uranium hexafluoride to either trimethylsilylchloride or trimethylsilylbromide in halocarbon solutions yield ..beta..-UF/sub 5/ at room temperature. With 2 mol equivalents of trimethylsilylchloride the product is UF/sub 4/. The reactions appear to proceed via the intermediate formation of unstable brown uranium(VI) chloride and bromide fluorides. Calculations show that UClF/sub 5/ and UCl/sub 2/F/sub 4/ are thermodynamically unstable with respect to the loss of chlorine at room temperature.

  9. Uranium hexafluoride and uranyl nitrate. Ionometric determination of bromine

    International Nuclear Information System (INIS)

    Anon.

    Bromine was determined in uranium hexafluoride. The method is suitable for determining 2 to 20 ppm with respect to uranium. Bromides are oxidized by potassium permanganate to give bromine which is extracted into carbon tetrachloride, reduced by ascorbic acid and determined by ionometry [fr

  10. Depleted uranium hexafluoride: Waste or resource?

    Energy Technology Data Exchange (ETDEWEB)

    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)

    1995-07-01

    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.

  11. Standard test method for the analysis of refrigerant 114, plus other carbon-containing and fluorine-containing compounds in uranium hexafluoride via fourier-transform infrared (FTIR) spectroscopy

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2004-01-01

    1.1 This test method covers determining the concentrations of refrigerant-114, other carbon-containing and fluorine-containing compounds, hydrocarbons, and partially or completely substituted halohydrocarbons that may be impurities in uranium hexafluoride. The two options are outlined for this test method. They are designated as Part A and Part B. 1.1.1 To provide instructions for performing Fourier-Transform Infrared (FTIR) spectroscopic analysis for the possible presence of Refrigerant-114 impurity in a gaseous sample of uranium hexafluoride, collected in a "2S" container or equivalent at room temperature. The all gas procedure applies to the analysis of possible Refrigerant-114 impurity in uranium hexafluoride, and to the gas manifold system used for FTIR applications. The pressure and temperatures must be controlled to maintain a gaseous sample. The concentration units are in mole percent. This is Part A. 1.2 Part B involves a high pressure liquid sample of uranium hexafluoride. This method can be appli...

  12. Corrosion of Al-7075 by uranium hexafluoride

    International Nuclear Information System (INIS)

    1989-01-01

    The results of the Al-7075 corrosion by uranium hexafluoride are presented in this work. The kinetic study shows that corrosion process occurs by two temperature dependent mechanism and that the alloy can be safely used up to 140 0 C. The corrosion film is formed by uranium oxifluoride with variable composition in depth. Two alternative corrosion models are proposed in order to explain the experimental results, as well as the tests taht will be carried out to confirm one of them [pt

  13. Preparation of sodium fluoride agglomerates for selective adsorption of uranium hexafluoride (U F6)

    International Nuclear Information System (INIS)

    Castro, A.R.; Maximiano, C.; Shimba, R.; Silva, E.R.F.

    1995-01-01

    Uranium hexafluoride (U F 6 ) and Sodium Fluoride (NaF) reacts reversibly to form a solid complex. Such reversibility accounts for the great interest in using Sodium Fluoride (NaF) to separate Uranium Hexafluoride (U F 6 ) from other gases. Therefore a chemical trap offers an alternative to the cryogenic trapping device. (author). 3 refs, 1 fig, 4 tabs

  14. Depleted uranium hexafluoride management program : data compilation for the Paducah site

    International Nuclear Information System (INIS)

    Hartmann, H.

    2001-01-01

    This report is a compilation of data and analyses for the Paducah site, near Paducah, Kentucky. The data were collected and the analyses were done in support of the U.S. Department of Energy (DOE) 1999 Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted Uranium Hexafluoride (DOE/EIS-0269). The report describes the affected environment at the Paducah site and summarizes potential environmental impacts that could result from conducting the following depleted uranium hexafluoride (UF 6 ) activities at the site: continued cylinder storage, preparation of cylinders for shipment, conversion, and long-term storage. DOE's preferred alternative is to begin converting the depleted UF 6 inventory as soon as possible to either uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible

  15. Depleted uranium hexafluoride management program : data compilation for the Portsmouth site

    International Nuclear Information System (INIS)

    Hartmann, H. M.

    2001-01-01

    This report is a compilation of data and analyses for the Portsmouth site, near Portsmouth, Ohio. The data were collected and the analyses were done in support of the U.S. Department of Energy (DOE) 1999 Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted Uranium Hexafluoride (DOE/EIS-0269). The report describes the affected environment at the Portsmouth site and summarizes potential environmental impacts that could result from conducting the following depleted uranium hexafluoride (UF 6 ) management activities at the site: continued cylinder storage, preparation of cylinders for shipment, conversion, and long-term storage. DOE's preferred alternative is to begin converting the depleted UF 6 inventory as soon as possible to either uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible

  16. Cost-effectiveness of safety measures applying to uranium hexafluoride transportation in France

    International Nuclear Information System (INIS)

    Hubert, P.; Pages, P.; Auguin, B.

    1983-01-01

    This paper addresses the problem of uranium hexafluoride transportation by truck and train. It consists of a probabilistic risk assessment of the potential hazards to the public that can arise from the traffice that will take place in France in 1990. The specificity of UF 6 is that it presents both chemical and radiological hazards. But, whatever the transported material, road traffic entails a risk of its own. Thus three kinds of risk are assessed for natural, depleted and enriched uranium hexafluoride. These assessments are the basis of a cost-effectiveness analysis which deals with such safety measures as using a protective overpack, avoiding populated area and escorting the trucks. The results presented here are based upon research supported by the C.E.A. (Commissariat a l'Energie Atomique). It is linked to a more general program of experiments and theoretical analyses on package safety and accidental releases for uranium hexafluoride. 7 references, 2 figures, 4 tables

  17. Investigation of transformation of uranium hexafluoride into dioxide

    International Nuclear Information System (INIS)

    Galkin, N.P.; Veryatin, U.D.; Yakhonin, I.F.; Logunov, A.F.; Dymkov, Yu.M.

    1982-01-01

    The process of transformation of uranium hexafluoride into dioxide using the method of pyrohydrolysis by steam-hydrogen mixture in a boiling layer using uranium dioxide granules applicable for production of fuel elements is considered. Technological parameters and equipment of the process are described, intermediate stages and process products are considered. Physicochemical and physicomechanical properties of the obtained uranium dioxide granules are given. The results of metallographical investigations into solid products of pyrohydrolysis in phase transformations at certain stages of the process as well as test on vibration packing of the obtained granules in fuel cans are presented

  18. Test emission of uranium hexafluoride in atmosphere. Results interpretation

    International Nuclear Information System (INIS)

    Crabol, B.; Deville-Cavelin, G.

    1989-01-01

    To permit the modelization of gaseous uranium hexafluoride behaviour in atmosphere, a validation test has been executed the 10 April 1987. The experimental conditions, the main results and a comparison with a diffusion model are given in this report [fr

  19. Management of wastes from the refining and conversion of uranium ore concentrate to uranium hexafluoride

    International Nuclear Information System (INIS)

    1981-01-01

    This report is the outcome of an IAEA Advisory Group Meeting on ''Waste Management Aspects in Relation to the Refining of Uranium Ore Concentrates and their Conversion to Uranium Hexafluoride'', which was held in Vienna from 17 to 21 December 1979. The report summarizes the main topics discussed at the meeting and gives an overview of uranium refining processes, being used in nuclear industry. The meeting was organized by the International Atomic Energy Agency, Radioactive Waste Management Section

  20. Summary of the engineering analysis report for the long-term management of depleted uranium hexafluoride

    International Nuclear Information System (INIS)

    Dubrin, J.W.; Rahm-Crites, L.

    1997-09-01

    The Department of Energy (DOE) is reviewing ideas for the long-term management and use of its depleted uranium hexafluoride. DOE owns about 560,000 metric tons (over a billion pounds) of depleted uranium hexafluoride. This material is contained in steel cylinders located in storage yards near Paducah, Kentucky; Portsmouth, Ohio; and at the East Tennessee Technology Park (formerly the K-25 Site) in Oak Ridge, Tennessee. On November 10, 1994, DOE announced its new Depleted Uranium Hexafluoride Management Program by issuing a Request for Recommendations and an Advance Notice of Intent in the Federal Register (59 FR 56324 and 56325). The first part of this program consists of engineering, costs and environmental impact studies. Part one will conclude with the selection of a long-term management plan or strategy. Part two will carry out the selected strategy

  1. Summary of the engineering analysis report for the long-term management of depleted uranium hexafluoride

    Energy Technology Data Exchange (ETDEWEB)

    Dubrin, J.W., Rahm-Crites, L.

    1997-09-01

    The Department of Energy (DOE) is reviewing ideas for the long-term management and use of its depleted uranium hexafluoride. DOE owns about 560,000 metric tons (over a billion pounds) of depleted uranium hexafluoride. This material is contained in steel cylinders located in storage yards near Paducah, Kentucky; Portsmouth, Ohio; and at the East Tennessee Technology Park (formerly the K-25 Site) in Oak Ridge, Tennessee. On November 10, 1994, DOE announced its new Depleted Uranium Hexafluoride Management Program by issuing a Request for Recommendations and an Advance Notice of Intent in the Federal Register (59 FR 56324 and 56325). The first part of this program consists of engineering, costs and environmental impact studies. Part one will conclude with the selection of a long-term management plan or strategy. Part two will carry out the selected strategy.

  2. World War II uranium hexafluoride inhalation event with pulmonary implications for today

    International Nuclear Information System (INIS)

    Moore, R.H.; Kathren, R.L.

    1985-01-01

    Two individuals were exposed to massive quantities of airborne uranium hexafluoride (UF6) and its hydrolysis products following a World War II equipment rupture. An excretion pattern for uranium exhibited by these patients is, in light of current knowledge, anomalous. The possible role of pulmonary edema is discussed. Examination of these individuals 38 years later showed no physical changes believed to be related to their uranium exposure and no deposition of uranium could be detected

  3. Research of heat releasing element of an active zone of gaseous nuclear reactor with pumped through nuclear fuel - uranium hexafluoride (UF6)

    International Nuclear Information System (INIS)

    Batyrbekov, G.; Batyrbekov, E.; Belyakova, E.; Kunakov, S.; Koltyshev, S.

    1996-01-01

    The purpose of the offered project is learning physics and substantiation of possibility of creation gaseous nuclear reactor with pumped through nuclear fuel-hexafluoride of uranium (Uf6).Main problems of this work are'. Determination of physic-chemical, spectral and optical properties of non-equilibrium nuclear - excited plasma of hexafluoride of uranium and its mixtures with other gases. Research of gas dynamics of laminar, non-mixing two-layer current of gases of hexafluoride of uranium and helium at availability and absence of internal energy release in hexafluoride of uranium with the purpose to determinate a possibility of isolation of hexafluoride of uranium from walls by inert helium. Creation and research of gaseous heat releasing element with pumped through fuel Uf6 in an active zone of research nuclear WWR-K reactor. Objects of a research: Non-equilibrium nuclear - excited plasma of hexafluoride of uranium and its mixtures with other gases. With use of specially created ampoules will come true in-reactor probe and spectral diagnostics of plasma. Calculations of kinetics with the account of main elementary processes proceeding in it, will be carried out. Two-layer non-mixed streams of hexafluoride of uranium and helium at availability and absence of internal energy release. Conditions of obtaining and characteristics of such streams will be investigated. Gaseous heat releasing element with pumped through fuel - Uf6 in an active zone of nuclear WWR-K reactor

  4. Depleted uranium hexafluoride management program : data compilation for the K-25 site

    International Nuclear Information System (INIS)

    Hartmann, H. M.

    2001-01-01

    This report is a compilation of data and analyses for the K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The data were collected and the analyses were done in support of the U.S. Department of Energy (DOE) 1999 Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted Uranium Hexafluoride (DOE/EIS-0269). The report describes the affected environment at the K-25 site and summarizes the potential environmental impacts that could result from continued cylinder storage and preparation of cylinders for shipment at the site. It is probable that the cylinders at the K-25 site will be shipped to another site for conversion. Because conversion and long-term storage of the entire inventory at the K-25 site are highly unlikely, these data are not presented in this report. DOE's preferred alternative is to begin converting the depleted uranium hexafluoride inventory as soon as possible to either uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible

  5. Nuclear fuel technology - Determination of uranium in solutions, uranium hexafluoride and solids - Part 2: Iron(II) reduction/cerium(IV) oxidation titrimetric method

    International Nuclear Information System (INIS)

    2004-01-01

    This first edition of ISO 7097-1 together with ISO 7097-2:2004 cancels and replaces ISO 7097:1983, which has been technically revised, and ISO 9989:1996. ISO 7097 consists of the following parts, under the general title Nuclear fuel technology - Determination of uranium in solutions, uranium hexafluoride and solids: Part 1: Iron(II) reduction/potassium dichromate oxidation titrimetric method; Part 2: Iron(II) reduction/cerium(IV) oxidation titrimetric method. This part 2. of ISO 7097 describes procedures for determination of uranium in solutions, uranium hexafluoride and solids. The procedures described in the two independent parts of this International Standard are similar: this part uses a titration with cerium(IV) and ISO 7097-1 uses a titration with potassium dichromate

  6. Nuclear fuel technology - Determination of uranium in solutions, uranium hexafluoride and solids - Part 1: Iron(II) reduction/potassium dichromate oxidation titrimetric method

    International Nuclear Information System (INIS)

    2004-01-01

    This first edition of ISO 7097-1 together with ISO 7097-2:2004 cancels and replaces ISO 7097:1983, which has been technically revised, and ISO 9989:1996. ISO 7097 consists of the following parts, under the general title Nuclear fuel technology - Determination of uranium in solutions, uranium hexafluoride and solids: Part 1: Iron(II) reduction/potassium dichromate oxidation titrimetric method; Part 2: Iron(II) reduction/cerium(IV) oxidation titrimetric method. This part 1. of ISO 7097 describes procedures for the determination of uranium in solutions, uranium hexafluoride and solids. The procedures described in the two independent parts of this International Standard are similar: this part uses a titration with potassium dichromate and ISO 7097-2 uses a titration with cerium(IV)

  7. Selection of a management strategy for depleted uranium hexafluoride

    International Nuclear Information System (INIS)

    Patton, S.E.; Hanrahan, E.J.; Bradley, C.E.

    1995-01-01

    A consequence of the uranium enrichment process used in the United States (US) is the accumulation of a significant amount of depleted uranium hexafluoride (UF 6 ). Currently, approximately 560,000 metric tons of the material are stored at three different sites. The US Department of Energy (DOE) has recently initiated a program to consider alternative strategies for the cost-effective and environmentally safe long-term management of this inventory of depleted UF 6 . The program involves a technology and engineering assessment of proposed management options (use/reuse, conversion, storage, or disposal) and an analysis of the potential environmental impacts and life-cycle costs of alternative management strategies. The information obtained from the studies will be used by the DOE to select a preferred long-term management strategy. The selection and implementation of a management strategy will involve consideration of a number of important issues such as environmental, health, and safety effects; the balancing of risks versus costs in a context of reduced government spending; socioeconomic implications, including effects on the domestic and international uranium industry; the technical status of proposed uses or technologies; and public involvement in the decision making process. Because of its provisions for considering a wide range of relevant issues and involving the public, this program has become a model for future DOE materials disposition programs. This paper presents an overview of the Depleted Uranium Hexafluoride Management Program. Technical findings of the program to date are presented, and major issues involved in selecting and implementing a management strategy are discussed

  8. A review of laser isotope separation of uranium hexafluoride

    International Nuclear Information System (INIS)

    Kelly, J.W.

    1983-04-01

    There is continuing world-wide interest in the possibility of enriching uranium by a laser process which uses uranium hexafluoride. Since no actual commercial plant exists at present, this review examines the key areas of related research. It concludes that such a process is feasible, that it must employ an adiabatic cooling system, with UF 6 the minor constituent in a predominantly monatomic or diatomic carrier gas, that the necessary infrared and/or ultraviolet-visible lasers are in a state of development bordering on the minimum required, and that the economics of such a process appear highly promising

  9. Processing device for gaseous waste containing uranium hexafluoride

    International Nuclear Information System (INIS)

    Hirosawa, Jun-ichi.

    1985-01-01

    Purpose: To enable to detect the inactivation of chemical traps thereby reduce the amount of adsorbents. Constitution: Two chemical traps are disposed in series and γ-detector for detecting γ-rays generated from U-235 in hexafluoride is disposed to the outer surface of a pipeway connecting these two chemical traps. Further, chemical traps are adapted to be swtichable between the first stage and the second stage thereof by the ON-OFF operation of a valve. Then, by determining γ-rays from U-235 at the pipeway downstream from the gas exit of the chemical traps, the counted value for the γ-rays is substantially at the background level so long as the chemical trap has an adsorbing performance for uranium hexafluoride. Then, since the γ-ray counted value is increased at the step upon inactivation of the chemical trap, the inactivation of the trap can be detected. (Yoshino, Y.)

  10. Criticality concerns in cleaning large uranium hexafluoride cylinders

    International Nuclear Information System (INIS)

    Sheaffer, M.K.; Keeton, S.C.; Lutz, H.F.

    1995-06-01

    Cleaning large cylinders used to transport low-enriched uranium hexafluoride (UF 6 ) presents several challenges to nuclear criticality safety. This paper presents a brief overview of the cleaning process, the criticality controls typically employed and their bases. Potential shortfalls in implementing these controls are highlighted, and a simple example to illustrate the difficulties in complying with the Double Contingency Principle is discussed. Finally, a summary of recommended criticality controls for large cylinder cleaning operations is presented

  11. Chemical toxicity of uranium hexafluoride compared to acute effects of radiation

    International Nuclear Information System (INIS)

    McGuire, S.A.

    1991-02-01

    The chemical effects from acute exposures to uranium hexafluoride are compared to the nonstochastic effects from acute radiation doses of 25 rems to the whole body and 300 rems to the thyroid. The analysis concludes that an intake of about 10 mg of uranium in soluble form is roughly comparable, in terms of early effects, to an acute whole body dose of 25 rems because both are just below the threshold for significant nonstochastic effects. Similarly, an exposure to hydrogen fluoride at a concentration of 25 mg/m 3 for 30 minutes is roughly comparable because there would be no significant nonstochastic effects. For times t other than 30 minutes, the concentration C of hydrogen fluoride considered to have the same effect can be calculated using a quadratic equation: C = 25 mg/m 3 (30 min/t). The purpose of these analyses is to provide information for developing design and siting guideline based on chemical toxicity for enrichment plants using uranium hexafluoride. These guidelines are to be similar, in terms of stochastic health effects, to criteria in NRC regulations of nuclear power plants, which are based on radiation doses. 26 refs., 1 fig., 5 tabs

  12. Chemical toxicity of uranium hexafluoride compared to acute effects of radiation

    Energy Technology Data Exchange (ETDEWEB)

    McGuire, S.A.

    1991-02-01

    The chemical effects from acute exposures to uranium hexafluoride are compared to the nonstochastic effects from acute radiation doses of 25 rems to the whole body and 300 rems to the thyroid. The analysis concludes that an intake of about 10 mg of uranium in soluble form is roughly comparable, in terms of early effects, to an acute whole body dose of 25 rems because both are just below the threshold for significant nonstochastic effects. Similarly, an exposure to hydrogen fluoride at a concentration of 25 mg/m{sup 3} for 30 minutes is roughly comparable because there would be no significant nonstochastic effects. For times t other than 30 minutes, the concentration C of hydrogen fluoride considered to have the same effect can be calculated using a quadratic equation: C = 25 mg/m{sup 3} (30 min/t). The purpose of these analyses is to provide information for developing design and siting guideline based on chemical toxicity for enrichment plants using uranium hexafluoride. These guidelines are to be similar, in terms of stochastic health effects, to criteria in NRC regulations of nuclear power plants, which are based on radiation doses. 26 refs., 1 fig., 5 tabs.

  13. Acute toxicity of uranium hexafluoride, uranyl fluoride and hydrogen fluoride

    International Nuclear Information System (INIS)

    Just, R.A.

    1988-01-01

    Uranium hexafluoride (UF 6 ) released into the atmosphere will react rapidly with moisture in the air to form the hydrolysis products uranyl fluoride (UO 2 F 2 ) and hydrogen fluoride (HF). Uranium compounds such as UF 6 and UO 2 F 2 exhibit both chemical toxicity and radiological effects, while HF exhibits only chemical toxicity. This paper describes the development of a methodology for assessing the human health consequences of a known acute exposure to a mixture of UF 6 , UO 2 F 2 , and HF. 4 refs., 2 figs., 5 tabs

  14. Depleted uranium hexafluoride: The source material for advanced shielding systems

    Energy Technology Data Exchange (ETDEWEB)

    Quapp, W.J.; Lessing, P.A. [Idaho National Engineering Lab., Idaho Falls, ID (United States); Cooley, C.R. [Department of Technology, Germantown, MD (United States)

    1997-02-01

    The U.S. Department of Energy (DOE) has a management challenge and financial liability problem 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. DOE is evaluating several options for the disposition of this UF{sub 6}, including continued storage, disposal, and recycle into a product. Based on studies conducted to date, the most feasible recycle option for the depleted uranium is shielding in low-level waste, spent nuclear fuel, or vitrified high-level waste containers. Estimates for the cost of disposal, using existing technologies, range between $3.8 and $11.3 billion depending on factors such as the disposal site and the applicability of the Resource Conservation and Recovery Act (RCRA). Advanced technologies can reduce these costs, but UF{sub 6} disposal still represents large future costs. This paper describes an application for depleted uranium in which depleted uranium hexafluoride is converted into an oxide and then into a heavy aggregate. The heavy uranium aggregate is combined with conventional concrete materials to form an ultra high density concrete, DUCRETE, weighing more than 400 lb/ft{sup 3}. DUCRETE can be used as shielding in spent nuclear fuel/high-level waste casks at a cost comparable to the lower of the disposal cost estimates. Consequently, the case can be made that DUCRETE shielded casks are an alternative to disposal. In this case, a beneficial long term solution is attained for much less than the combined cost of independently providing shielded casks and disposing of the depleted uranium. Furthermore, if disposal is avoided, the political problems associated with selection of a disposal location are also avoided. Other studies have also shown cost benefits for low level waste shielded disposal containers.

  15. Uranium hexafluoride: handling procedures and container criteria

    International Nuclear Information System (INIS)

    1977-04-01

    The U.S. Energy Research and Development Administration's (ERDA) procedures for packaging, measuring, and transferring uranium hexafluoride (UF 6 ) have been undergoing continual review and revision for several years to keep them in phase with developing agreements for the supply of enriched uranium. This report, first issued in 1966, was reissued in 1967 to make editorial changes and to provide for minor revisions in procedural information. In 1968 and 1972, Revisions 2 and 3, respectively, were issued as part of the continuing effort to present updated information. This document, Revision 4, includes primarily revisions to UF 6 cylinders, valves, and methods of use. This revision supersedes all previous issues of this report. The procedures will normally apply in all transactions involving receipt or shipment of UF 6 by ERDA, unless stipulated otherwise by contracts or agreements with ERDA or by notices published in the Federal Register

  16. Study of the molecular structure of uranium hexafluoride

    International Nuclear Information System (INIS)

    Bougon, R.

    1967-06-01

    The vibrational spectrum of uranium hexafluoride has been studied in both the gaseous and solid states. The study of gaseous UF 6 confirms the regular octahedral structure of the fluorine atoms around the central U atom and makes it possible to evaluate some of the vibrational frequencies. From these, some new force constants have been determined. A tetragonal distortion is observed on solid UF 6 ; this distortion has only observed up till now by means of X-ray diffraction and nuclear magnetic resonance techniques. (author) [fr

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

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2011-01-01

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

  18. Hazard analysis in uranium hexafluoride production facility

    International Nuclear Information System (INIS)

    Marin, Maristhela Passoni de Araujo

    1999-01-01

    The present work provides a method for preliminary hazard analysis of nuclear fuel cycle facilities. The proposed method identify both chemical and radiological hazards, as well as the consequences associated with accident scenarios. To illustrate the application of the method, a uranium hexafluoride production facility was selected. The main hazards are identified and the potential consequences are quantified. It was found that, although the facility handles radioactive material, the main hazards as associated with releases of toxic chemical substances such as hydrogen fluoride, anhydrous ammonia and nitric acid. It was shown that a contention bung can effectively reduce the consequences of atmospheric release of toxic materials. (author)

  19. Standard model for safety analysis report of hexafluoride power plants from natural uranium

    International Nuclear Information System (INIS)

    1983-01-01

    The standard model for safety analysis report for hexafluoride production power plants from natural uranium is presented, showing the presentation form, the nature and the degree of detail, of the minimal information required by the Brazilian Nuclear Energy Commission - CNEN. (E.G.) [pt

  20. Kinetics of gaseous uranium hexafluoride reaction with hydrogen chloride

    International Nuclear Information System (INIS)

    Ezubchenko, A.N.; Ilyukhin, A.I.; Merzlyakov, A.V.

    1993-01-01

    Kinetics of decrease of concentration of gaseous uranium hexafluoride in reaction with hydrogen chloride at temperatures close to room ones, was investigated by the method of IR spectroscopy. It was established that the process represented the first order reaction by both UF 6 and HCl. Activation energy of the reaction was determined: 7.6 ± 0.7 kcal/mol. Specific feature of reaction kinetics was noted: inversely proportional dependence of effective constant on UF 6 initial pressure. 5 refs., 3 figs

  1. Uranium fluoride chemistry. Part 1. The gas phase reaction of uranium hexafluoride with alcohols

    International Nuclear Information System (INIS)

    Schnautz, N.G.; Venter, P.J.

    1992-01-01

    The reaction between uranium hexafluoride (UF 6 ) and simple alcohols in the gas phase was observed to proceed by way of three possible reaction pathways involving dehydration, deoxygenative fluorination, and ether formation. These reactions can best be explained by assuming that alcohols first react with UF 6 to afford the alkoxy uranium pentafluoride intermediate ROUF 5 , which reacts further to give the dehydration, deoxygenative fluorination, and ether products. In each of the above three reaction pathways, UF 6 is transformed to UOF 4 , which being as reactive toward alcohols as UF 6 , reacts further with the alcohol in question to finally afford the unreactive uranyl fluoride (UO 2 F 2 ). 6 refs., 2 tabs

  2. Cost update technology, safety, and costs of decommissioning a reference uranium hexafluoride conversion plant

    International Nuclear Information System (INIS)

    Miles, T.L.; Liu, Y.

    1995-08-01

    The purpose of this study is to update the cost estimates developed in a previous report, NUREG/CR-1757 (Elder 1980) for decommissioning a reference uranium hexafluoride conversion plant from the original mid-1981 dollars to values representative of January 1993. The cost updates were performed by using escalation factors derived from cost index trends over the past 11.5 years. Contemporary price quotes wee used for costs that have increased drastically or for which is is difficult to find a cost trend. No changes were made in the decommissioning procedures or cost element requirements assumed in NUREG/CR-1757. This report includes only information that was changed from NUREG/CR-1757. Thus, for those interested in detailed descriptions and associated information for the reference uranium hexafluoride conversion plant, a copy of NUREG/CR-1757 will be needed

  3. A system for the synthesis of uranium hexafluoride by high pressure fluorination of uranium oxides

    International Nuclear Information System (INIS)

    Elizalde T, J.; Saniger B, J.M.; Nava S, R.

    1986-01-01

    An equipment for the synthesis of uranium hexafluoride by a direct fluorination method is reported. The equipment is composed by a gaseous fluorine supply, a gas burette, a reactor tube inside a protective shield, a soda-lime chemical trap and a vacuum system. The fluorination is accomplished at a pressure of about 70 kg/cm 2 (1000 lb in 2 ), using gaseous fluorine. (Author). 5 refs, 4 figs, 2 tabs

  4. Study of reactions for the obtention of uranium tetrafluoride and hexafluoride

    International Nuclear Information System (INIS)

    Guzella, M.F.R.

    1984-01-01

    Based on an exhaustive bibliographical review, the main production processes of uranium hexafluoride in pilot plants and industrial facilities are described. The known reactions, confirmed in laboratory experiments, that lead to UF 6 or other intermediate fluorides, are presented and discussed. In order to determine a new thermodinamically feasible reaction involving the sulfur hexafluoride as fluorinating agent, a mock-up facility was designed and constructed as part of the R and D work planned at CDTN (NUCLEBRAS Center for Nuclear Technology Development, MG - Brazil). For the UF 4 synthesis employing U 3 O 8 and SF 6 , several experimental parameters were studied. The reaction time, gas flow, temperature and stoichiometric relations among reagents are described in detail. Suggestions for further investigations regarding this new reagent are made. (Author) [pt

  5. Dry uranium tetrafluoride process preparation using the uranium hexafluoride reconversion process effluents; Processo alternativo para obtencao de tetrafluoreto de uranio a partir de efluentes fluoretados da etapa de reconversao de uranio

    Energy Technology Data Exchange (ETDEWEB)

    Silva Neto, Joao Batista da

    2008-07-01

    It is a well known fact that the use of uranium tetrafluoride allows flexibility in the production of uranium suicide and uranium oxide fuel. To its obtention there are two conventional routes, the one which reduces uranium from the UF{sub 6} hydrolysis solution with stannous chloride, and the hydro fluorination of a solid uranium dioxide. In this work we are introducing a third and a dry way route, mainly utilized to the recovery of uranium from the liquid effluents generated in the uranium hexafluoride reconversion process, at IPEN/CNEN-SP. Working in the liquid phase, this route comprises the recuperation of ammonium fluoride by NH{sub 4}HF{sub 2} precipitation. Working with the solid residues, the crystallized bifluoride is added to the solid UO{sub 2}, which comes from the U mini plates recovery, also to its conversion in a solid state reaction, to obtain UF{sub 4}. That returns to the process of metallic uranium production unity to the U{sub 3}Si{sub 2} obtention. This fuel is considered in IPEN CNEN/SP as the high density fuel phase for IEA-R1m reactor, which will replace the former low density U{sub 3}Si{sub 2}-Al fuel. (author)

  6. Emission characteristics of uranium hexafluoride at high temperatures

    International Nuclear Information System (INIS)

    Krascella, N.L.

    1976-01-01

    An experimental study was conducted to ascertain the spectral characteristics of uranium hexafluoride (UF 6 ) and possible UF 6 thermal decomposition products as a function of temperature and pressure. Relative emission measurements were made for UF 6 /Argon mixtures heated in a plasma torch over a range of temperatures from 800 to about 3600 0 K over a wavelength range from 80 to 600 nm. Total pressures were varied from 1 to approximately 1.7 atm. Similarly absorption measurements were carried out in the visible region from 420 to 580 nm over a temperature range from about 1000 to 1800 0 K. Total pressure for these measurements was 1.0 atm

  7. Reuse of ammonium fluoride generated in the uranium hexafluoride conversion

    International Nuclear Information System (INIS)

    Silva Neto, J.B.; Carvalho, E.F. Urano de; Durazzo, M.; Riella, H.G

    2010-01-01

    The Nuclear Fuel Centre of IPEN / CNEN - SP develops and manufactures dispersion fuel with high uranium concentration to meet the demand of the IEA-R1 reactor and future research reactors planned to be constructed in Brazil. The fuel uses uranium silicide (U 3 Si 2 ) dispersed in aluminum. For producing the fuel, the processes for uranium hexafluoride (UF 6 ) conversion consist in obtaining U 3 Si 2 and / or U 3 O 8 through the preparation of intermediate compounds, among them ammonium uranyl carbonate - AUC, ammonium diuranate - DUA and uranium tetrafluoride - UF 4 . This work describes a procedure for preparing uranium tetrafluoride by a dry route using as raw material the filtrate generated when producing routinely ammonium uranyl carbonate. The filtrate consists primarily of a solution containing high concentrations of ammonium (NH 4 + ), fluoride (F - ), carbonate (CO 3 -- ) and low concentrations of uranium. The procedure is basically the recovery of NH 4 F and uranium, as UF 4 , through the crystallization of ammonium bifluoride (NH 4 HF 2 ) and, in a later step, the addition of UO 2 , occurring fluoridation and decomposition. The UF 4 obtained is further diluted in the UF 4 produced routinely at IPEN / CNEN-SP by a wet route process. (author)

  8. Minimizing the risk and impact of uranium hexafluoride production

    International Nuclear Information System (INIS)

    Clark, D.R.; Kennedy, T.W.

    2010-01-01

    Cameco Corporation's Port Hope conversion facility, situated on the shore of Lake Ontario in the Municipality of Port Hope, Ontario, Canada, converts natural uranium trioxide (UO_3) into uranium dioxide (UO_2) or natural uranium hexafluoride (UF_6). Conversion of UO_3 to UF_6 has been undertaken at the Port Hope conversion facility since 1970 and is currently carried out in a second-generation plant licensed to annually produce 12,500 tonnes U as UF_6. Consistent with Cameco's vision, values and measures of success, Cameco recognizes safety and health of its workers and the public, protection of the environment, and the quality of our processes as the highest corporate priorities. Production of UF_6 in a brownfield urban setting requires a commitment to design, build and maintain multiple layers of containment (defence-in-depth) and to continually improve in all operational aspects to achieve this corporate commitment. This paper will describe the conversion processes utilized with a focus on the cultural, management and physical systems employed to minimize the risk and impact of the operation. (author)

  9. Previsional evaluation of risks associated with ground transportation of uranium hexafluoride

    International Nuclear Information System (INIS)

    Pages, P.; Tomachevsky, E.

    1987-11-01

    This communication is a concrete example of application of the evaluation method for risks associated with road transportation of uranium hexafluoride by 48Y shipping container. The statistical bases for UF6 transportation are given by analysis of the list of accidents for dangerous road transportation. This study examines all parameters (cost-safety-meteorology-radiation doses) to take in account in the safety analysis of the UF6 transportation between Pierrelatte and Le Havre [fr

  10. Moderation control in low enriched 235U uranium hexafluoride packaging operations and transportation

    International Nuclear Information System (INIS)

    Dyer, R.H.; Kovac, F.M.; Pryor, W.A.

    1993-01-01

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

  11. Dynamic tests for qualifying of national uranium hexafluoride

    International Nuclear Information System (INIS)

    Araujo Figueiredo, C. de; Abreu Mendonca Schvartzman, M.M. de; Vasconcelos, M.C.R.L.

    1990-01-01

    The dynamic behaviour of the Brazilian uranium hexafluoride is analyzed in this paper, with regard to its radiolytic decomposition and to the action of catalysts on the reaction between UF 6 and H 2 . The process gas (UF 6 /H 2 ) was submitted in the laboratory of dynamic tests (DV-II) to similar conditions as those used in the enrichment plant presently being erected in Resende - RJ, 'First Cascade - FC'. The tests carried out have shown that the Brazilian UF 6 has the same dynamic behaviour of the German UF 6 . It does not contain either any catalyst of the reaction between UF 6 and H 2 which could render it inappropriate for use in commercial plants. (author) [pt

  12. Standard test methods for arsenic in uranium hexafluoride

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2005-01-01

    1.1 These test methods are applicable to the determination of total arsenic in uranium hexafluoride (UF6) by atomic absorption spectrometry. Two test methods are given: Test Method A—Arsine Generation-Atomic Absorption (Sections 5-10), and Test Method B—Graphite Furnace Atomic Absorption (Appendix X1). 1.2 The test methods are equivalent. The limit of detection for each test method is 0.1 μg As/g U when using a sample containing 0.5 to 1.0 g U. Test Method B does not have the complete collection details for precision and bias data thus the method appears as an appendix. 1.3 Test Method A covers the measurement of arsenic in uranyl fluoride (UO2F2) solutions by converting arsenic to arsine and measuring the arsine vapor by flame atomic absorption spectrometry. 1.4 Test Method B utilizes a solvent extraction to remove the uranium from the UO2F2 solution prior to measurement of the arsenic by graphite furnace atomic absorption spectrometry. 1.5 Both insoluble and soluble arsenic are measured when UF6 is...

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

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2010-01-01

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

  14. Uranium hexafluoride: Handling procedures and container descriptions

    International Nuclear Information System (INIS)

    1987-09-01

    The US Department of Energy (DOE) guidelines for packaging, measuring, and transferring uranium hexafluoride (UF 6 ) have been undergoing continual review and revision for several years to keep them in phase with developing agreements for the supply of enriched uranium. Initially, K-1323 ''A Brief Guide to UF 6 Handling,'' was issued in 1957. This was superceded by ORO-651, first issued in 1966, and reissued in 1967 to make editorial changes and to provide minor revisions in procedural information. In 1968 and 1972, Revisions 2 and 3, respectively, were issued as part of the continuing effort to present updated information. Revision 4 issued in 1977 included revisions to UF 6 cylinders, valves, and methods to use. Revision 5 adds information dealing with pigtails, overfilled cylinders, definitions and handling precautions, and cylinder heel reduction procedures. Weighing standards previously presented in ORO-671, Vol. 1 (Procedures for Handling and Analysis of UF 6 ) have also been included. This revision, therefore, supercedes ORO-671-1 as well as all prior issues of this report. These guidelines will normally apply in all transactions involving receipt or shipment of UF 6 by DOE, unless stipulated otherwise by contracts or agreements with DOE or by notices published in the Federal Register. Any questions or requests for additional information on the subject matter covered herein should be directed to the United States Department of Energy, P.O. Box E, Oak Ridge, Tennessee 37831, Attention: Director, Uranium Enrichment Operations Division. 33 figs., 12 tabs

  15. Automatic liquid nitrogen feeding device

    International Nuclear Information System (INIS)

    Gillardeau, J.; Bona, F.; Dejachy, G.

    1963-01-01

    An automatic liquid nitrogen feeding device has been developed (and used) in the framework of corrosion tests realized with constantly renewed uranium hexafluoride. The issue was to feed liquid nitrogen to a large capacity metallic trap in order to condensate uranium hexafluoride at the exit of the corrosion chambers. After having studied various available devices, a feeding device has been specifically designed to be robust, secure and autonomous, as well as ensuring a high liquid nitrogen flowrate and a highly elevated feeding frequency. The device, made of standard material, has been used during 4000 hours without any problem [fr

  16. Uranium hexafluoride: Safe handling, processing, and transporting: Conference proceedings

    Energy Technology Data Exchange (ETDEWEB)

    Strunk, W.D.; Thornton, S.G. (eds.)

    1988-01-01

    This conference seeks to provide a forum for the exchange of information and ideas of the safety aspects and technical issue related to the handling of uranium hexafluoride. By allowing operators, engineers, scientists, managers, educators, and others to meet and share experiences of mutual concern, the conference is also intended to provide the participants with a more complete knowledge of technical and operational issues. The topics for the papers in the proceedings are widely varied and include the results of chemical, metallurgical, mechanical, thermal, and analytical investigations, as well as the developed philosophies of operational, managerial, and regulatory guidelines. Papers have been entered individually into EDB and ERA. (LTN)

  17. Uranium hexafluoride: Safe handling, processing, and transporting: Conference proceedings

    International Nuclear Information System (INIS)

    Strunk, W.D.; Thornton, S.G.

    1988-01-01

    This conference seeks to provide a forum for the exchange of information and ideas of the safety aspects and technical issue related to the handling of uranium hexafluoride. By allowing operators, engineers, scientists, managers, educators, and others to meet and share experiences of mutual concern, the conference is also intended to provide the participants with a more complete knowledge of technical and operational issues. The topics for the papers in the proceedings are widely varied and include the results of chemical, metallurgical, mechanical, thermal, and analytical investigations, as well as the developed philosophies of operational, managerial, and regulatory guidelines. Papers have been entered individually into EDB and ERA

  18. Parametric analyses of planned flowing uranium hexafluoride critical experiments

    Science.gov (United States)

    Rodgers, R. J.; Latham, T. S.

    1976-01-01

    Analytical investigations were conducted to determine preliminary design and operating characteristics of flowing uranium hexafluoride (UF6) gaseous nuclear reactor experiments in which a hybrid core configuration comprised of UF6 gas and a region of solid fuel will be employed. The investigations are part of a planned program to perform a series of experiments of increasing performance, culminating in an approximately 5 MW fissioning uranium plasma experiment. A preliminary design is described for an argon buffer gas confined, UF6 flow loop system for future use in flowing critical experiments. Initial calculations to estimate the operating characteristics of the gaseous fissioning UF6 in a confined flow test at a pressure of 4 atm, indicate temperature increases of approximately 100 and 1000 K in the UF6 may be obtained for total test power levels of 100 kW and 1 MW for test times of 320 and 32 sec, respectively.

  19. Some parameters of uranium hexafluoride plasma produced by products of nuclear reaction

    International Nuclear Information System (INIS)

    Batyrbekov, G.A.; Belyakova, Eh.A.

    1996-01-01

    The probe experimental results of investigation of uranium hexafluoride plasma produced in the centre of nuclear reactor core were demonstrated. Study of uranium hexafluoride plasma is continued by the following reasons: a possibility of U F 6 utilization as nuclear fuel, the utilization of U F 6 as volume source o ionization, search of active laser media compatible with U F 6 that is complicated by lack of constant rates data for most of plasma-chemical reactions with U F 6 and his dissociation products. Cylindrical probe volt-ampere characteristics (VAC) measured in U F 6 plasma at pressure 20 Torr and different thermal neutron fluxes and have following features: -firstly, it is possible to choose a linear part in the field of small positive potentials of probe (0-1) V; - secondary, ion branches of VAC have typical break which current of satiation corresponds to; -thirdly, probe VAC measured at small values of thermal neutron flux density are symmetrical. Diagnostics approaches were used for interpretation VAC of probe. The values of satiation current and linear part of electron branch were calculated, and such plasma parameters as conductivity, diffusion coefficient values of positive and negative ions were determined. The resonance recharge cross section was estimated on diffusion coefficient value

  20. Uranium hexafluoride packaging tiedown systems overview at Portsmouth Gaseous Diffusion Plant, Piketon, Ohio

    International Nuclear Information System (INIS)

    Becker, D.L.; Green, D.J.; Lindquist, M.R.

    1993-07-01

    The Portsmouth Gaseous Diffusion Plant (PORTS) in Piketon, Ohio, is operated by Martin Marietta Energy Systems, Inc., through the US Department of Energy-Oak Ridge Operations Office (DOE-ORO) for the US Department of Energy-Headquarters, Office of Nuclear Energy. The PORTS conducts those operations that are necessary for the production, packaging, and shipment of uranium hexafluoride (UF 6 ). Uranium hexafluoride enriched uranium than 1.0 wt percent 235 U shall be packaged in accordance with the US Department of Transportation (DOT) regulations of Title 49 CFR Parts 173 (Reference 1) and 178 (Reference 2), or in US Nuclear Regulatory Commission (NRC) or US Department of Energy (DOE) certified package designs. Concerns have been expressed regarding the various tiedown methods and condition of the trailers being used by some shippers/carriers for international transport of the UF 6 cylinders/overpacks. Because of the concerns about international shipments, the US Department of Energy-Headquarters (DOE-HQ) Office of Nuclear Energy, through DOE-HQ Transportation Management Division, requested Westinghouse Hanford Company (Westinghouse Hanford) to review UF 6 packaging tiedown and shipping practices used by PORTS, and where possible and appropriate, provide recommendations for enhancing these practices. Consequently, a team of two individuals from Westinghouse Hanford visited PORTS on March 5 and 6, 1990, for the purpose of conducting this review. The paper provides a brief discussion of the review activities and a summary of the resulting findings and recommendations. A detailed reporting of the is documented in Reference 4

  1. Infrared analysis of hydrogen fluoride in uranium hexafluoride

    International Nuclear Information System (INIS)

    Ohwada, Ken; Soga, Takeshi; Iwasaki, Matae; Tsujimura, Shigeo

    1975-01-01

    Quantitative analysis by infrared technique was made on hydrogen fluoride (HF) contained in uranium hexafluoride (UF 6 ). It was found that, among the vibration-rotation bands, the R(1)-, R(2)-, P(2)- and P(3)-branches having relatively large absorbances are convenient for the analysis of HF. Upon comparing the calibration curves of pure HF with the HF absorbances observed in the presence of UF 6 (approx. 70--100 Torr), N 2 (approx. 100 Torr) and Ar(approx. 100 Torr) gases, it was observed that the first-mentioned calibration curve could be applied to the analysis of HF when mixed with other substances, as in the latter cases. The detectable limits of HF pressure, using a infrared cell of 10cm path length, were 0.5--1 Torr at room temperature. (auth.)

  2. Formation of actinide hexafluorides at ambient temperatures with krypton difluoride

    International Nuclear Information System (INIS)

    Asprey, L.B.; Eller, P.G.; Kinkead, S.A.

    1986-01-01

    A second low-temperature agent, krypton difluoride, for generating volatile plutonium hexafluoride is reported (dioxygen difluoride is the only other reported agent). Plutonium hexafluoride is formed at ambient or lower temperature by the treatment of various solid substrates with krypton difluoride. Volatilization of uranium and neptunium from solid substrates using gaseous krypton difluoride is also reported for the first time. The formation of actinide hexafluorides has been confirmed for the reaction of krypton difluoride in anhydrous HF with UO 2 and with uranium and neptunium fluorides at ambient temperatures. Treatment of americium dioxide with krypton difluoride did not yield americium hexafluoride under the conditions studied. 15 references, 2 figures

  3. Status of overpacks for uranium hexafluoride transport

    International Nuclear Information System (INIS)

    Arendt, J.W.; Pryor, W.A.

    1985-01-01

    The original overpacks for uranium hexafluoride (UF 6 ) transport, which utilized phenolic foam insulation, were developed in the 1960's and ultimately became international standards. A second generation of overpacks for 10-ton-capacity UF 6 cylinders used polyurethane foam and was developed in the early 1970's. In the mid 1970's, a third generation was designed, but no attempt to develop it occurred until the early 1980's, when full-scale testing of an overpack for 14-ton capacity UF 6 cylinders was initiated and resulted in designs for a new family of UF 6 overpacks. In the meantime, two additional developments affected overpack use for UF 6 cylinder transport: (1) the discovery that phenolic-foam-insulated overpacks have water absorption and outleakage problems inaugurated a program for their improvement and (2) new polyurethane-insulated overpacks were manufactured. The current status of all these overpacks, including their designs, testing, and approval for transport is presented

  4. Estimates of health risks associated with uranium hexafluoride transport by air

    International Nuclear Information System (INIS)

    Elert, M.; Skagius, K.

    1990-01-01

    In Sweden air transport is considered as an alternative for the shipment of uranium hexafluoride (UF 6 ). The radiological consequences of an aeroplane accident involving UF 6 transport have been estimated and are presented as the dose from acute exposure and the dose from long-term exposure caused by ground contamination. Chemical effects of a UF 6 release are also discussed. A number of limiting scenarios have been defined, resulting in different mechanical and thermal impacts on the transport packages. The expected accident environment and the physical and chemical behaviour of the material have been used to derive a source term for the release to the air. A Gaussian dispersion model has been used to calculate the expected air concentration downwind from the accident site. The radiation dose from short-term exposure was found to be higher than the long-term exposure from uranium deposited on the ground. (author)

  5. Estimating the threshold levels of uranium and fluorine for the development of pulmonitis and toxic lung edema resultant from accidents involving uranium hexafluoride release

    International Nuclear Information System (INIS)

    Gasteva, G.N.; Antipin, E.B.; Bad'in, V.I.; Molokanov, A.A.; Mordasheva, V.V.; Mirkhajdarov, A.Kh.; Sorokin, A.V.; Savinova, I.A.

    1999-01-01

    Threshold doses of uranium and fluorine for the development of pulmonitis and toxic edema of the lung with lethal outcome are estimated. The levels of UF 6 entry under emergency conditions are evaluated and bronchopulmonary disease is described in subjects involved in three accidents with UF 6 release which occurred in the seventies and eighties, as shown by records. The results deny the previous assumption on the leading role of uranium in a single exposure to uranium hexafluoride. Fluorine ion triggering the mechanism of reactions in systems which determine the disease outcome is vitally important [ru

  6. Including environmental concerns in management strategies for depleted uranium hexafluoride

    International Nuclear Information System (INIS)

    Goldberg, M.; Avci, H.I.; Bradley, C.E.

    1995-01-01

    One of the major programs within the Office of Nuclear Energy, Science, and Technology of the US Department of Energy (DOE) is the depleted uranium hexafluoride (DUF 6 ) management program. The program is intended to find a long-term management strategy for the DUF 6 that is currently stored in approximately 46,400 cylinders at Paducah, KY; Portsmouth, OH; and Oak Ridge, TN, USA. The program has four major components: technology assessment, engineering analysis, cost analysis, and the environmental impact statement (EIS). From the beginning of the program, the DOE has incorporated the environmental considerations into the process of strategy selection. Currently, the DOE has no preferred alternative. The results of the environmental impacts assessment from the EIS, as well as the results from the other components of the program, will be factored into the strategy selection process. In addition to the DOE's current management plan, other alternatives continued storage, reuse, or disposal of depleted uranium, will be considered in the EIS. The EIS is expected to be completed and issued in its final form in the fall of 1997

  7. The physical and chemical properties of uranium hexafluoride

    International Nuclear Information System (INIS)

    Barber, E.J.

    1988-01-01

    This paper describes what uranium hexafluoride (UF 6 ) is, gives some of its pertinent physical properties, illustrates significant reactions between UF 6 and other substances, touches on its toxic properties, and states some of the ''do's'' and ''don't's'' of UF 6 handling. The properties of UF 6 determine how it must be handled and make direct observation impossible. To determine that the material in a container is UF 6 , one must use other instruments in addition to a scale. Because of the very large volume expanision of UF 6 upon melting, diligence must be exercised in filling cylinders in which the UF 6 is partially solidified. A cylinder of liquified UF 6 with no ullage is potentially the equivalent of a superheated hot water heater, not just a hydraulically overpressurized cylinder. Finally, UF 6 can be handled safely by careful attention to the suggested precautions. 9 refs., 2 tabs., 3 figs

  8. Evaluation of health effects in Sequoyah Fuels Corporation workers from accidental exposure to uranium hexafluoride

    International Nuclear Information System (INIS)

    Fisher, D.R.; Swint, M.J.; Kathren, R.L.

    1990-05-01

    Urine bioassay measurements for uranium and medical laboratory results were studied to determine whether there were any health effects from uranium intake among a group of 31 workers exposed to uranium hexafluoride (UF 6 ) and hydrolysis products following the accidental rupture of a 14-ton shipping cylinder in early 1986 at the Sequoyah Fuels Corporation uranium conversion facility in Gore, Oklahoma. Physiological indicators studied to detect kidney tissue damage included tests for urinary protein, casts and cells, blood, specific gravity, and urine pH, blood urea nitrogen, and blood creatinine. We concluded after reviewing two years of follow-up medical data that none of the 31 workers sustained any observable health effects from exposure to uranium. The early excretion of uranium in urine showed more rapid systemic uptake of uranium from the lung than is assumed using the International Commission on Radiological Protection (ICRP) Publication 30 and Publication 54 models. The urinary excretion data from these workers were used to develop an improved systemic recycling model for inhaled soluble uranium. We estimated initial intakes, clearance rates, kidney burdens, and resulting radiation doses to lungs, kidneys, and bone surfaces. 38 refs., 10 figs., 7 tabs

  9. Evaluation of health effects in Sequoyah Fuels Corporation workers from accidental exposure to uranium hexafluoride

    Energy Technology Data Exchange (ETDEWEB)

    Fisher, D.R. (Pacific Northwest Lab., Richland, WA (USA)); Swint, M.J.; Kathren, R.L. (Hanford Environmental Health Foundation, Richland, WA (USA))

    1990-05-01

    Urine bioassay measurements for uranium and medical laboratory results were studied to determine whether there were any health effects from uranium intake among a group of 31 workers exposed to uranium hexafluoride (UF{sub 6}) and hydrolysis products following the accidental rupture of a 14-ton shipping cylinder in early 1986 at the Sequoyah Fuels Corporation uranium conversion facility in Gore, Oklahoma. Physiological indicators studied to detect kidney tissue damage included tests for urinary protein, casts and cells, blood, specific gravity, and urine pH, blood urea nitrogen, and blood creatinine. We concluded after reviewing two years of follow-up medical data that none of the 31 workers sustained any observable health effects from exposure to uranium. The early excretion of uranium in urine showed more rapid systemic uptake of uranium from the lung than is assumed using the International Commission on Radiological Protection (ICRP) Publication 30 and Publication 54 models. The urinary excretion data from these workers were used to develop an improved systemic recycling model for inhaled soluble uranium. We estimated initial intakes, clearance rates, kidney burdens, and resulting radiation doses to lungs, kidneys, and bone surfaces. 38 refs., 10 figs., 7 tabs.

  10. Metabolic fate and evaluation of injury in rats and dogs following exposure to the hydrolysis products of uranium hexafluoride: implications for a bioassay program related to potential releases of uranium hexafluoride, July 1979-October 1981

    International Nuclear Information System (INIS)

    Morrow, P.E.; Leach, L.J.; Smith, F.A.

    1982-12-01

    This final report summarizes the experimental studies undertaken in rats and dogs in order to help provide adequate biological bases for quantifying and evaluating uranium hexafluoride (UF 6 ) exposures. Animals were administered the hydrolysis products of UF 6 by inhalation exposures, intratracheal instillations and intravenous injections. Attention was given to dose-effect relationships appropriate to the kidney, the unique site of subacute toxicity; to the rates of uranium excretion; and to uranium retention in renal tissue. These criteria were examined in both naive and multiply-exposed animals. The findings of these studies partly substantiate the ICRP excretion model for hexavalent uranium; generally provide a lower renal injury threshold concentration than implicit in the MPC for natural uranium; indicate distinctions in response (for example, uranium excretion) are based on exposure history; compare and evaluate various biochemical indices of renal injury; raise uncertainties about prevailing views of reversible renal injury, renal tolerance and possible hydrogen fluoride synergism with uranium effects; and reveal species differences in several areas, for example, renal retention of uranium. While these studies present some complicating features to extant bioassay practice, they nevertheless supply data supportive of the bioassay concept

  11. Uranium hexafluoride production plant decommissioning

    International Nuclear Information System (INIS)

    Santos, Ivan

    2008-01-01

    The Institute of Energetic and Nuclear Research - IPEN is a research and development institution, located in a densely populated area, in the city of Sao Paulo. The nuclear fuel cycle was developed from the Yellow Cake to the enrichment and reconversion at IPEN. After this phase, all the technology was transferred to private enterprises and to the Brazilian Navy (CTM/SP). Some plants of the fuel cycle were at semi-industrial level, with a production over 20 kg/h. As a research institute, IPEN accomplished its function of the fuel cycle, developing and transferring technology. With the necessity of space for the implementation of new projects, the uranium hexafluoride (UF 6 ) production plant was chosen, since it had been idle for many years and presented potential leaking risks, which could cause environmental aggression and serious accidents. This plant decommission required accurate planning, as this work had not been carried out in Brazil before, for this type of facility, and there were major risks involving gaseous hydrogen fluoride aqueous solution of hydrofluoric acid (HF) both highly corrosive. Evaluations were performed and special equipment was developed, aiming to prevent leaking and avoid accidents. During the decommissioning work, the CNEN safety standards were obeyed for the whole operation. The environmental impact was calculated, showing to be not relevant.The radiation doses, after the work, were within the limits for the public and the area was released for new projects. (author)

  12. Final programmatic environmental impact statement for alternative strategies for the long-term management and use of depleted uranium hexafluoride. Summary

    International Nuclear Information System (INIS)

    1999-04-01

    This PEIS assesses the potential impacts of alternative management strategies for depleted uranium hexafluoride (UF 6 ) currently stored at three DOE sites: Paducah site near Paducah, Kentucky, Portsmouth site near Portsmouth, Ohio; and K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The alternatives analyzed in the PEIS include no action, long-term storage as UF 6 , long-term storage as uranium oxide, use as uranium oxide, use as uranium metal, and disposal. DOE's preferred alternative is to begin conversion of the depleted UF 6 inventory as soon as possible, either to uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible

  13. Production of sized particles of uranium oxides and uranium oxyfluorides

    International Nuclear Information System (INIS)

    Knudsen, I.E.; Randall, C.C.

    1976-01-01

    A process is claimed for converting uranium hexafluoride (UF 6 ) to uranium dioxide (UO 2 ) of a relatively large particle size in a fluidized bed reactor by mixing uranium hexafluoride with a mixture of steam and hydrogen and by preliminary reacting in an ejector gaseous uranium hexafluoride with steam and hydrogen to form a mixture of uranium and oxide and uranium oxyfluoride seed particles of varying sizes, separating the larger particles from the smaller particles in a cyclone separator, recycling the smaller seed particles through the ejector to increase their size, and introducing the larger seed particles from the cyclone separator into a fluidized bed reactor where the seed particles serve as nuclei on which coarser particles of uranium dioxide are formed. 9 claims, 2 drawing figures

  14. Production of uranium hexafluoride by fluorination tetra-fluoride with elemental fluorine under pressure; Proizvodnja uraovega heksafluorida s tlacnim fluoriranjem uranovega tetrafluorida z elementarnim fluorom

    Energy Technology Data Exchange (ETDEWEB)

    Lutar, K; Smalc, A; Zemljic, A [Institut Jozef Stefan, Ljubljana (Yugoslavia)

    1984-07-01

    In the introduction a brief description of some activities of fluorine chemistry department at the J. Stefan Institute is given - from production of elemental fluorine to the investigations in the field of uranium technology. Furthermore, a new method for the production of uranium hexafluoride is described more in detail. The method is based on the fluorination of uranium tetrafluoride with elemental fluorine. (author)

  15. Depleted uranium hexafluoride (DUF6) management system--a decision tool

    International Nuclear Information System (INIS)

    Gasper, J.R.; Sutter, R.J.; Avci, H.I.

    1995-01-01

    The Depleted Uranium Hexafluoride (DUF 6 ) Management System (DMS) is being developed as a decision tool to provide cost and risk data for evaluation of short-and long-term management strategies for depleted uranium. It can be used to assist decision makers on a programmatic or site-specific level. Currently, the DMS allows evaluation of near-term cylinder management strategies such as storage yard improvements, cylinder restocking, and reconditioning. The DMS has been designed to provide the user with maximum flexibility for modifying data and impact factors (e.g., unit costs and risk factors). Sensitivity analysis can be performed on all key parameters such as cylinder corrosion rate, inspection frequency, and impact factors. Analysis may be conducted on a system-wide, site, or yard basis. The costs and risks from different scenarios may be compared in graphic or tabular format. Ongoing development of the DMS will allow similar evaluation of long-term management strategies such as conversion to other chemical forms. The DMS is a Microsoft Windows 3.1 based, stand-alone computer application. It can be operated on a 486 or faster computer with VGA, 4 MB of RAM, and 10 MB of disk space

  16. Fire testing of bare uranium hexafluoride cylinders

    Energy Technology Data Exchange (ETDEWEB)

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

    1991-12-31

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

  17. Fire testing of bare uranium hexafluoride cylinders

    Energy Technology Data Exchange (ETDEWEB)

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

    1991-12-31

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

  18. Uranium hexafluoride packaging tiedown systems overview at Portsmouth Gaseous Diffusion Plant, Piketon, Ohio

    International Nuclear Information System (INIS)

    Becker, D.L.; Lindquist, M.R.

    1993-01-01

    The Portsmouth Gaseous Diffusion Plant (PORTS) in Piketon, Ohio, is operated by Martin Marietta Energy Systems, Inc., through the US Department of Energy-Oak Ridge Operations Office (DOE-ORO) for the US Department of Energy-Headquarters, Office of Nuclear Energy. The PORTS conducts those operations that are necessary for the production, packaging, and shipment of enriched uranium hexafluoride (UF 6 ). Uranium hexafluoride enriched greater than 1.0 wt percent 235 U shall be packaged in accordance with the US Department of Transportation (DOT) regulations of Title 49 CFR Parts 173 and 178, or in US Nuclear Regulatory Commission (NRC) or US Department of Energy (DOE) certified package designs. Concerns have been expressed regarding the various tiedown methods and condition of the trailers being used by some shippers/carriers for international transport of the UF 6 cylinders/overpacks. International shipments typically are not made using dedicated trailers, and numerous trailers have been received at PORTS with improperly and potentially dangerously secured overpacks. Because of the concerns about international shipments, the US Department of Energy-Headquarters (DOE-HQ) Office of Nuclear Energy, through DOE-HQ Transportation Management Division, requested Westinghouse Hanford Company (Westinghouse Hanford) to review UF 6 packaging tiedown and shipping practices used by PORTS; and where possible and appropriate, provide recommendations for enhancing these practices. Consequently, a team of two individuals from Westinghouse Hanford visited PORTS on March 5 and 6, 1990, for the purpose of conducting this review. The paper provides a brief discussion of the review activities and a summary of the resulting findings and recommendations

  19. Isotopic analysis of uranium hexafluoride highly enriched in U-235

    International Nuclear Information System (INIS)

    Chaussy, L.; Boyer, R.

    1968-01-01

    Isotopic analysis of uranium in the form of the hexafluoride by mass-spectrometry gives gross results which are not very accurate. Using a linear interpolation method applied to two standards it is possible to correct for this inaccuracy as long as the isotopic concentrations are less than about 10 per cent in U-235. Above this level, the interpolations formula overestimates the results, especially if the enrichment of the analyzed samples is higher than 1.3 with respect to the standards. A formula is proposed for correcting the interpolation equation and for the extending its field of application to high values of the enrichment (≅2) and of the concentration. It is shown that by using this correction the results obtained have an accuracy which depends practically only on that of the standards, taking into account the dispersion in the measurements. (authors) [fr

  20. Assessment of the risk of transporting uranium hexafluoride by truck and train

    International Nuclear Information System (INIS)

    Geffen, C.A.; Johnson, J.F.; Davis, D.K.; Friley, J.R.; Ross, B.A.

    1978-08-01

    This report is the fifth in a series of studies of the risk of transporting potentially hazardous energy materials. The report presents an assessment of the risk of shipping uranium hexafluoride (UF 6 ) by truck and rail. The general risk assessment methodology, summarized in Section 3, used in this study is that developed for the first study in this series. The assessment includes the risks from release of uranium hexafluoride during truck or rail transport due to transportation accidents. The contribution to the risk of deteriorated or faulty packaging during normal transport was also considered. The report is sectioned to correspond to the specific analysis steps of the risk assessment model. The transportation system and accident environment are described in Sections 4 and 5. Calculation of the response of the shipping system to forces produced in transportation accidents are presented in Section 6 and the results of a survey to determine the condition of the package during transport are presented in Section 7. Sequences of events that could lead to a release of radioactive material from the shipping cask during transportation are postulated in Section 8 using fault tree analysis. These release sequences are evaluated in Sections 9 through 11, to determine both the likelihood and the possible consequences of each release. Supportive data and analyses are given in the appendices. The results of the risk assessment have been related to the year 1985, when it is projected that 100 GW of electric power will be generated annually by nuclear power plants. It was estimated that approximately 46,000 metric tons (MT) of natural UF 6 and 14,600 MT of enriched UF 6 would be shipped in the reference year

  1. TRIMOLECULAR REACTIONS OF URANIUM HEXAFLUORIDE WITH WATER

    Energy Technology Data Exchange (ETDEWEB)

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

    2010-02-25

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

  2. Some Investigations of the Reaction of Activated Charcoal with Fluorine and Uranium Hexafluoride

    Energy Technology Data Exchange (ETDEWEB)

    Del Cul, G.D.; Fiedor, J.N.; Simmons, D.W.; Toth, L.M.; Trowbridge, L.D.; Williams

    1998-09-01

    The Molten Salt Reactor Experiment (MSRE) at Oak Ridge National Laboratory has been shut down since 1969, when the fuel salt was drained from the core into two Hastelloy N drain tanks at the reactor site. Over time, fluorine (F{sub 2}) and uranium hexafluoride (UF{sub 6}) moved from the salt through the gas piping to a charcoal bed, where they reacted with the activated charcoal. Some of the immediate concerns related to the migration of F{sub 2} and UF{sub 6} to the charcoal bed were the possibility of explosive reactions between the charcoal and F{sub 2}, the existence of conditions that could induce a criticality accident, and the removal and recovery of the fissile uranium from the charcoal. This report addresses the reactions and reactivity of species produced by the reaction of fluorine and activated charcoal and between charcoal and F{sub 2}-UF{sub 6} gas mixtures in order to support remediation of the MSRE auxiliary charcoal bed (ACB) and the recovery of the fissile uranium. The chemical identity, stoichiometry, thermochemistry, and potential for explosive decomposition of the primary reaction product, fluorinated charcoal, was determined.

  3. Some Investigations of the Reaction of Activated Charcoal with Fluorine and Uranium Hexafluoride

    International Nuclear Information System (INIS)

    Del Cul, G.D.; Fiedor, J.N.; Simmons, D.W.; Toth, L.M.; Trowbridge, L.D.; Williams

    1998-01-01

    The Molten Salt Reactor Experiment (MSRE) at Oak Ridge National Laboratory has been shut down since 1969, when the fuel salt was drained from the core into two Hastelloy N drain tanks at the reactor site. Over time, fluorine (F 2 ) and uranium hexafluoride (UF 6 ) moved from the salt through the gas piping to a charcoal bed, where they reacted with the activated charcoal. Some of the immediate concerns related to the migration of F 2 and UF 6 to the charcoal bed were the possibility of explosive reactions between the charcoal and F 2 , the existence of conditions that could induce a criticality accident, and the removal and recovery of the fissile uranium from the charcoal. This report addresses the reactions and reactivity of species produced by the reaction of fluorine and activated charcoal and between charcoal and F 2 -UF 6 gas mixtures in order to support remediation of the MSRE auxiliary charcoal bed (ACB) and the recovery of the fissile uranium. The chemical identity, stoichiometry, thermochemistry, and potential for explosive decomposition of the primary reaction product, fluorinated charcoal, was determined

  4. Process for decontamination of surfaces in an facility of natural uranium hexafluoride production (UF6)

    International Nuclear Information System (INIS)

    Almeida, Claudio C. de; Silva, Teresinha M.; Rodrigues, Demerval L.; Carneiro, Janete C.G.G.

    2017-01-01

    The experience acquired in the actions taken during the decontamination process of an IPEN-CNEN / SP Nuclear and Energy Research Institute facility, for the purpose of making the site unrestricted, is reported. The steps of this operation involved: planning, training of facility operators, workplace analysis and radiometric measurements. The facility had several types of equipment from the natural uranium hexafluoride (UF 6 ) production tower and other facility materials. Rules for the transportation of radioactive materials were established, both inside and outside the facility and release of materials and installation

  5. F19 relaxation in non-magnetic hexafluorides

    International Nuclear Information System (INIS)

    Rigny, P.

    1969-01-01

    The interesting properties of the fluorine magnetic resonance in the hexafluorides of molybdenum, tungsten and uranium, are very much due to large anisotropies of the chemical shift tensors. In the solid phases these anisotropies, the values of which are deduced from line shape studies, allow one to show that the molecules undergo hindered rotations about the metal atom. The temperature and frequency dependence of the fluorine longitudinal relaxation times shows that the relaxation is due to the molecular motion. The dynamical parameters of this motion are then deduced from the complete study of the fluorine relaxation in the rotating frame. In the liquid phases, the existence of anisotropies allows an estimation of the different contributions to the relaxation. In particular, the frequency and temperature dependence of the relaxation shows it to be dominated by the spin-rotation interaction. We have shown that the strength of this interaction can be deduced from the chemical shifts, and the angle through which the molecule rotates quasi-freely can be determined. In the hexafluorides, this angle is roughly one radian at 70 C, and with the help of this value, the friction coefficients which describe the intermolecular interactions are discussed. (author) [fr

  6. Final programmatic environmental impact statement for alternative strategies for the long-term management and use of depleted uranium hexafluoride. Volume 2: Appendices

    International Nuclear Information System (INIS)

    1999-04-01

    This PEIS assesses the potential impacts of alternative management strategies for depleted uranium hexafluoride (UF 6 ) currently stored at three DOE sites: Paducah site near Paducah, Kentucky, Portsmouth site near Portsmouth, Ohio; and K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The alternatives analyzed in the PEIS include no action, long-term storage as UF 6 , long-term storage as uranium oxide, use as uranium oxide, use as uranium metal, and disposal. DOE's preferred alternative is to begin conversion of the depleted UF 6 inventory as soon as possible, either to uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible. This volume contains Appendices A--O

  7. Draft Programmatic Environmental Impact Statement for alternative strategies for the long-term management and use of depleted uranium hexafluoride. Volume 1: Main text

    International Nuclear Information System (INIS)

    1997-12-01

    This PEIS assesses the potential impacts of alternative management of alternative management strategies for depleted uranium hexafluoride (UF 6 ) currently stored at three DOE sites: Paducah site near Paducah, Kentucky; Portsmouth site near Portsmouth, Ohio; and K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The alternatives analyzed in the PEIS include no action, long-term storage as UF 6 , long-term storage as uranium oxide, use as uranium oxide, use as uranium metal, and disposal. The preferred alternative for the long-term management of depleted UF 6 is to use the entire inventory of material

  8. Final programmatic environmental impact statement for alternative strategies for the long-term management and use of depleted uranium hexafluoride. Volume 1: Main text

    International Nuclear Information System (INIS)

    1999-04-01

    This PEIS assesses the potential impacts of alternative management strategies for depleted uranium hexafluoride (UF 6 ) currently stored at three DOE sites: Paducah site near Paducah, Kentucky, Portsmouth site near Portsmouth, Ohio; and K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The alternatives analyzed in the PEIS include no action, long-term storage as UF 6 , long-term storage as uranium oxide, use as uranium oxide, use as uranium metal, and disposal. DOE's preferred alternative is to begin conversion of the depleted UF 6 inventory as soon as possible, either to uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible

  9. Draft Programmatic Environmental Impact Statement for alternative strategies for the long-term management and use of depleted uranium hexafluoride. Volume 2: Appendices

    International Nuclear Information System (INIS)

    1997-12-01

    This PEIS assesses the potential impacts of alternative management of alternative management strategies for depleted uranium hexafluoride (UF 6 ) currently stored at three DOE sites: Paducah site near Paducah, Kentucky; Portsmouth site near Portsmouth, Ohio; and K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The alternatives analyzed in the PEIS include no action, long-term storage as UF 6 , long-term storage as uranium oxide, use as uranium oxide, use as uranium metal, and disposal. The preferred alternative for the long-term management of depleted UF 6 is to use the entire inventory of material. This volume contains the appendices to volume I

  10. Chemisorption of uranium hexa-fluoride on sodium fluoride pellets

    Energy Technology Data Exchange (ETDEWEB)

    Kalburgi, A K; Sanyal, A; Puranik, V D; Bhattacharjee, B [Chemical Technology Division, Bhabha Atomic Research Centre, Mumbai (India)

    1994-06-01

    This paper comprises kinetics of chemical reaction or rather chemisorption of uranium hexafluoride gas on sodium fluoride pellets. The chemisorption is essentially irreversible at room temperature, while the process reverses at high temperature above 280 deg C. This chemisorption process was experimentally conducted in static condition at room temperature and its kinetics was studied. In the experiments, practically pure UF{sub 6} was used and the effects of gas pressure and weight of NaF pellets, were studied. In this heterogenous reaction, in which diffusion through ash layer is followed by chemical reaction, the reaction part is instantaneous and is first order with respect to gas concentration. Since the process of chemisorption is not only pure chemical reaction but also gas diffusion through ash layer, the rate constant depreciates with the percentage loading of UF{sub 6} on NaF pellets. The kinetic equation for the above process has been established for a particular size of NaF pellets and pellet porosity. (author). 5 refs., 3 figs., 3 tabs.

  11. Uniform deposition of uranium hexafluoride (UF6): Standardized mass deposits and controlled isotopic ratios using a thermal fluorination method

    Energy Technology Data Exchange (ETDEWEB)

    McNamara, Bruce K.; O’Hara, Matthew J.; Casella, Andrew M.; Carter, Jennifer C.; Addleman, R. Shane; MacFarlan, Paul J.

    2016-07-01

    Abstract: We report a convenient method for the generation of volatile uranium hexafluoride (UF6) from solid uranium oxides and other uranium compounds, followed by uniform deposition of low levels of UF6 onto sampling coupons. Under laminar flow conditions, UF6 is shown to interact with surfaces within the chamber to a highly predictable degree. We demonstrate the preparation of uranium deposits that range between ~0.01 and 470±34 ng∙cm-2. The data suggest the method can be extended to creating depositions at the sub-picogram∙cm-2 level. Additionally, the isotopic composition of the deposits can be customized by selection of the uranium source materials. We demonstrate a layering technique whereby two uranium solids, each with a different isotopic composition, are employed to form successive layers of UF6 on a surface. The result is an ultra-thin deposit of UF6 that bears an isotopic signature that is a composite of the two uranium sources. The reported deposition method has direct application to the development of unique analytical standards for nuclear safeguards and forensics.

  12. Stabilization of uranium hexafluoride by hydrolysis method for decommissioning of safeguard laboratory facility

    Energy Technology Data Exchange (ETDEWEB)

    Inagawa, Jun; Hotoku, Shinobu; Oda, Tetsuzo; Aoyagi, Noboru; Magara, Masaaki [Japan Atomic Energy Agency, Nuclear Science and Engineering Directorate, Tokai, Ibaraki (Japan)

    2014-03-15

    In safeguard laboratory (SGL) facility of Nuclear Science Research Institute of JAEA , uranium hexafluoride (UF{sub 6}) of enriched uranium of various enrichment was used for research and development of a spectrometric method for the determination of the enrichment of uranium in April 1983 through March 1993. After completion of this R and D, the UF{sub 6} has been stored in SGL facility. It was decided that the UF{sub 6} is carried to out of the facility, because the SGL facility will be decommissioning until March 2015. To transport and store in safety after transportation, it is necessary that the UF{sub 6} should be converted to stable chemical form. Hydrolysis of UF{sub 6} to uranyl fluoride (UO{sub 2}F{sub 2}) and evaporation to solid state were selected for the stabilization method. The equipment for hydrolysis and evaporation was installed in the SGL facility. Stabilization was operated in this equipment, and all of the UF{sub 6} in the SGL facility was converted to UO{sub 2}F{sub 2} solid state in October 2012 through August 2013. In this report, results of examination and operation for stabilization of UF{sub 6} were reported. (author)

  13. Preconceptual design studies and cost data of depleted uranium hexafluoride conversion plants

    International Nuclear Information System (INIS)

    Jones, E

    1999-01-01

    One of the more important legacies left with the Department of Energy (DOE) after the privatization of the United States Enrichment Corporation is the large inventory of depleted uranium hexafluoride (DUF6). The DOE Office of Nuclear Energy, Science and Technology (NE) is responsible for the long-term management of some 700,000 metric tons of DUF6 stored at the sites of the two gaseous diffusion plants located at Paducah, Kentucky and Portsmouth, Ohio, and at the East Tennessee Technology Park in Oak Ridge, Tennessee. The DUF6 management program resides in NE's Office of Depleted Uranium Hexafluoride Management. The current DUF6 program has largely focused on the ongoing maintenance of the cylinders containing DUF6. However, the long-term management and eventual disposition of DUF6 is the subject of a Programmatic Environmental Impact Statement (PEIS) and Public Law 105-204. The first step for future use or disposition is to convert the material, which requires construction and long-term operation of one or more conversion plants. To help inform the DUF6 program's planning activities, it was necessary to perform design and cost studies of likely DUF6 conversion plants at the preconceptual level, beyond the PEIS considerations but not as detailed as required for conceptual designs of actual plants. This report contains the final results from such a preconceptual design study project. In this fast track, three month effort, Lawrence Livermore National Laboratory and Bechtel National Incorporated developed and evaluated seven different preconceptual design cases for a single plant. The preconceptual design, schedules, costs, and issues associated with specific DUF6 conversion approaches, operating periods, and ownership options were evaluated based on criteria established by DOE. The single-plant conversion options studied were similar to the dry-conversion process alternatives from the PEIS. For each of the seven cases considered, this report contains information on

  14. Study of the molecular structure of uranium hexafluoride; Contribution a l'etude de la structure moleculaire de l'hexafluorure d'uranium

    Energy Technology Data Exchange (ETDEWEB)

    Bougon, R [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1967-06-01

    The vibrational spectrum of uranium hexafluoride has been studied in both the gaseous and solid states. The study of gaseous UF{sub 6} confirms the regular octahedral structure of the fluorine atoms around the central U atom and makes it possible to evaluate some of the vibrational frequencies. From these, some new force constants have been determined. A tetragonal distortion is observed on solid UF{sub 6}; this distortion has only observed up till now by means of X-ray diffraction and nuclear magnetic resonance techniques. (author) [French] Le spectre de vibration de l'hexafluorure d'uranium UF{sub 6} est etudie sous les formes gazeuse et solide. L'etude de l'UF{sub 6} gaz confirme la structure d'octaedre regulier d'atomes de fluor autour de l'atome central d'uranium et apporte une precision sur certaines frequences de vibration. A partir de ces valeurs, de nouvelles determinations de constantes de force ont ete realisees. L'observation de UF{sub 6} solide confirme la deformation tetragonale de l'octaedre, deformation observee jusqu'a present par les seules methodes de resonance magnetique nucleaire et diffraction des rayons X. (auteur)

  15. Uranium hexafluoride: A manual of good handling practices. Revision 7

    International Nuclear Information System (INIS)

    1995-01-01

    The United States Enrichment Corporation (USEC) is continuing the policy of the US Department of Energy (DOE) and its predecessor agencies in sharing with the nuclear industry their experience in the area of uranium hexafluoride (UF 6 ) shipping containers and handling procedures. The USEC has reviewed Revision 6 or ORO-651 and is issuing this new edition to assure that the document includes the most recent information on UF 6 handling procedures and reflects the policies of the USEC. This manual updates the material contained in earlier issues. It covers the essential aspects of UF 6 handling, cylinder filling and emptying, general principles of weighing and sampling, shipping, and the use of protective overpacks. The physical and chemical properties of UF 6 are also described. The procedures and systems described for safe handling of UF 6 presented in this document have been developed and evaluated during more than 40 years of handling vast quantities of UF 6 . With proper consideration for its nuclear properties, UF 6 may be safely handled in essentially the same manner as any other corrosive and/or toxic chemical

  16. Compilation of Requirements for Safe Handling of Fluorine and Fluorine-Containing Products of Uranium Hexafluoride Conversion

    International Nuclear Information System (INIS)

    Ferrada, J.J.; Hightower, J.R.; Begovich, J.M.

    2000-01-01

    Public Law (PL) 105--204 requires the U.S. Department of Energy to develop a plan for inclusion in the fiscal year 2000 budget for conversion of the Department's stockpile of depleted uranium hexafluoride (DUF6) to a more stable form over an extended period. The conversion process into a more stable form will produce fluorine compounds (e.g., elemental fluorine or hydrofluoric acid) that need to be handled safely. This document compiles the requirements necessary to handle these materials within health and safety standards, which may apply in order to ensure protection of the environment and the safety and health of workers and the public

  17. Uranium hexafluoride: A manual of good handling practices. Revision 7

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-01-01

    The United States Enrichment Corporation (USEC) is continuing the policy of the US Department of Energy (DOE) and its predecessor agencies in sharing with the nuclear industry their experience in the area of uranium hexafluoride (UF{sub 6}) shipping containers and handling procedures. The USEC has reviewed Revision 6 or ORO-651 and is issuing this new edition to assure that the document includes the most recent information on UF{sub 6} handling procedures and reflects the policies of the USEC. This manual updates the material contained in earlier issues. It covers the essential aspects of UF{sub 6} handling, cylinder filling and emptying, general principles of weighing and sampling, shipping, and the use of protective overpacks. The physical and chemical properties of UF{sub 6} are also described. The procedures and systems described for safe handling of UF{sub 6} presented in this document have been developed and evaluated during more than 40 years of handling vast quantities of UF{sub 6}. With proper consideration for its nuclear properties, UF{sub 6} may be safely handled in essentially the same manner as any other corrosive and/or toxic chemical.

  18. Rupture of Model 48Y UF6 cylinder and release of uranium hexafluoride, Sequoyah Fuels Facility, Gore, Oklahoma, January 4, 1986. Volume 1

    International Nuclear Information System (INIS)

    1986-02-01

    At 11:30 a.m. on January 4, 1986, a Model 48Y UF 6 cylinder filled with uranium hexafluoride (UF 6 ) ruptured while it was being heated in a steam chest at the Sequoyah Fuels Conversion Facility near Gore, Oklahoma. One worker died because he inhaled hydrogen fluoride fumes, a reaction product of UF 6 and airborne moisture. Several other workers were injured by the fumes, but none seriously. Much of the facility complex and some offsite areas to the south were contaminated with hydrogen fluoride and a second reaction product, uranyl fluoride. The interval of release was approximately 40 minutes. The cylinder, which had been overfilled, ruptured while it was being heated because of the expansion of UF 6 as it changed from the solid to the liquid phase. The maximum safe capacity for the cylinder is 27,560 pounds of product. Evidence indicates that it was filled with an amount exceeding this limit. 18 figs

  19. Uranium hexafluoride - chemistry and technology of a raw material of the nuclear fuel cycle

    International Nuclear Information System (INIS)

    Bacher, W.; Jacob, E.

    1986-01-01

    Uranium hexafluoride exhibits an unusual combination of properties: UF 6 is both a large-scale industrial product, and also one of the most reactive compounds known. Its industrial application arises from the need to use enriched uranium with up to 4% 235 U as fuel in light water reactors. Enrichment is performed in isotope separation plants with UF 6 as the working gas. Its volatility and thermal stability make UF 6 suitable for this application. UF 6 handling is difficult because of its high reactivity and its radioactivity, and special experience and equipment are required which are not commonly available in laboratories or industrial facilities. The chemical reactions of UF 6 are characterized by its marked fluorination efficiency which is similar to that of F 2 . Of special importance in connection with the handling of UF 6 is its extreme sensitivity to hydrolysis. Because they all use UF 6 , the isotope separation processes currently in use (gas diffusion, gas centrifuge, separation nozzle process) have a number of common features. For instance, they are all beset by the problem of formation of solid UF 6 decomposition products, e.g. by radiolysis of UF 6 molecules induced by its own radiation. Reconversion of UF 6 into UO 2 is achieved by three well-known methods (ADU, AUC, IDP-process). To produce uranium metal, UF 6 is first reduced to UF 4 , which is subsequently reduced by Ca 6 or Mg metal. 158 refs

  20. Standard test method for gamma energy emission from fission products in uranium hexafluoride and uranyl nitrate solution

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2005-01-01

    1.1 This test method covers the measurement of gamma energy emitted from fission products in uranium hexafluoride (UF6) and uranyl nitrate solution. It is intended to provide a method for demonstrating compliance with UF6 specifications C 787 and C 996 and uranyl nitrate specification C 788. 1.2 The lower limit of detection is 5000 MeV Bq/kg (MeV/kg per second) of uranium and is the square root of the sum of the squares of the individual reporting limits of the nuclides to be measured. The limit of detection was determined on a pure, aged natural uranium (ANU) solution. The value is dependent upon detector efficiency and background. 1.3 The nuclides to be measured are106Ru/ 106Rh, 103Ru,137Cs, 144Ce, 144Pr, 141Ce, 95Zr, 95Nb, and 125Sb. Other gamma energy-emitting fission nuclides present in the spectrum at detectable levels should be identified and quantified as required by the data quality objectives. 1.4 This standard does not purport to address all of the safety concerns, if any, associated with its us...

  1. Morse-Morse-Spline-Van der Waals intermolecular potential suitable for hexafluoride gases

    International Nuclear Information System (INIS)

    Coroiu, Ilioara

    2004-01-01

    Several effective isotopic pair potential functions have been proposed to characterize the bulk properties of quasispherical molecules, in particular the hexafluorides, but none got a success. Unfortunately, these potentials have repulsive walls steeper than those which describe the hexafluorides. That these intermolecular potentials are not quite adequate is shown by the lack of complete agreement between theory and experiment even for the rare gases. Not long ago, R. A. Aziz et al. have constructed a Morse-Morse-Spline-Van der Waals (MMSV) potential. The MMSV potential incorporates the determination of C 6 dispersion coefficient and it reasonably correlates second virial coefficients and viscosity data of sulphur hexafluoride at the same time. None of the potential functions previously proposed in literature could predict these properties simultaneously. We calculated the second virial coefficients and a large number of Chapman-Cowling collision integrals for this improved intermolecular potential, the MMSV potential. The results were tabulated for a large reduced temperature range, kT/ε from 0.1 to 100. The treatment was entirely classical and no corrections for quantum effects were made. The higher approximations to the transport coefficients and the isotopic thermal diffusion factor were also calculated and tabulated for the same range. In this paper we present the evaluation of the uranium hexafluoride potential parameters for the MMSV intermolecular potential. To find a single set of potential parameters which could predict all the transport properties (viscosity, thermal conductivity, self diffusion, etc.), as well as the second virial coefficients, simultaneously, the method suggested by Morizot and a large assortment of literature data were used. Our results emphasized that the Morse-Morse-Spline-Van der Waals potential have the best overall predictive ability for gaseous hexafluoride data, certain for uranium hexafluoride. (author)

  2. Safety analysis report on the ''Paducah Tiger'' overpack for 10-ton cylinder of uranium hexafluoride

    International Nuclear Information System (INIS)

    Stitt, D.H.

    1978-01-01

    A summary of analysis performed to assess the puncture resistance of the Paducah Tiger under a particularly severe (worst case) orientation of the external puncture pin is presented. The six-inch diameter cylindrical puncture pin has been oriented to place its impact location immediately opposite the valve body mounted to the dished head of the uranium hexafluoride cylinder. The valve body is assumed to have a one-inch clearance relative to the inner wall of the overpack. Analysis indicates that significant residual kinetic energy remains in the system at the instant of overpack inner wall contact with the valve body. Thus, there is strong evidence suggesting that the valve body can be damaged, or sheared from the dished head of the UF 6 , under the assumed worst case impact orientation

  3. Hydraulic breakage of tanks for the transport of uranium hexafluoride (UF6)

    International Nuclear Information System (INIS)

    Biaggio, A.L.; Lee Gonzales, H.M.; Lopez Vietri, J.R.; Novo, R.G.

    1987-01-01

    To begin with, the tank models that are proposed by the international norms for the transport and storage of hexafluoride of uranium (UF 6 ) are briefly described. The operations related to the transport in its different forms are also described, particularly those that can produce the hydraulic breakage of tanks during its course or in later stages, when incorrectly performed. With reference to those operations, the most important physicochemical properties of UF 6 as for safety are analyzed. A quantitative evaluation of the deviations of parameters that are controlled during the heating of tanks, comparing them with the normative nominal values, is performed. Adopting some simplifying hypothesis, a general study, applicable to all tank models proposed by norms, is carried out to determine the temperature at which the hydraulic breakage takes place when they are heated in closed-valve conditions. A curve is obtained by plotting the hydraulic breakage temperature against the filling degree. To conclude, the values obtained are compared with the results of other theoretical studies on this subject. (Author)

  4. Evaluation of a redesigned 3/4-inch uranium hexafluoride cylinder valve stem

    International Nuclear Information System (INIS)

    Zonner, L.A.; Wamsley, S.D.

    1978-01-01

    The performance of a redesigned 3/4-in. uranium hexafluoride cylinder valve stem has been evaluated at the Portsmouth Gaseous Diffusion Plant. Prototypes, machined from Monel bar stock and having a 45 0 tip angle instead of the 15 0 tip angle of the standard valve stem, were fabricated. Tests included: cyclic leak evaluation; flow restriction determination; wear testing with uranyl fluoride deposits in the valve seat; stress corrosion testing; field testing (in previously rejected valve bodies); and production leak testing. Because their overall test performance was excellent, actual production usage of the redesigned stems was initiated. The in-service performance of valves fitted with redesigned stems has been significantly superior to that of valves having the standard stems: rejection rates have been 0.7 and 16.6 percent, respectively. Recommendations are made to replace all 15 0 angle tip stems presently in service with new stems having a 45 0 angle tip and to specify the new stem tip design for future 3/4-in. valve purchases

  5. A concept of a nonfissile uranium hexafluoride overpack for storage, transport, and processing of corroded cylinders

    International Nuclear Information System (INIS)

    Pope, R.B.; Cash, J.M.; Singletary, B.H.

    1996-01-01

    There is a need to develop a means of safely transporting breached 48-in. cylinders containing depleted uranium hexafluoride (UF 6 ) from current storage locations to locations where the contents can be safely removed. There is also a need to provide a method of safely and easily transporting degraded cylinders that no longer meet the US Department of Transportation (DOT) and American National Standards Institute, Inc., (ANSI) requirements for shipments of depleted UF 6 . A study has shown that an overpack can be designed and fabricated to satisfy these needs. The envisioned overpack will handle cylinder models 48G, 48X, and 48Y and will also comply with the ANSI N14.1 and the American Society of Mechanical Engineers (ASME) Sect. 8 requirements

  6. Development of on-line uranium enrichment monitor of gaseous UF6 for uranium enrichment plant

    International Nuclear Information System (INIS)

    Lu Xuesheng; Liu Guorong; Jin Huimin; Zhao Yonggang; Li Jinghuai; Hao Xueyuan; Ying Bin; Yu Zhaofei

    2013-01-01

    An on-line enrichment monitor was developed to measure the enrichment of UF 6 , flowing through the processing pipes in uranium enrichment plant. A Nal (Tl) detector was used to measure the count rates of the 185.7 keV γ-ray emitted from 235 U, and the total quantity of uranium was determined from thermodynamic characteristics of gaseous uranium hexafluoride. The results show that the maximum relative standard deviation is less than 1% when the measurement time is 120 s or more and the pressure is more than 2 kPa in the measurement chamber. Uranium enrichment of gaseous uranium hexafluoride in the output end of cascade can be monitored continuously by using the device. It should be effective for nuclear materials accountability verifications and materials balance verification at uranium enrichment plant. (authors)

  7. Interim guidance on the safe transport of uranium hexafluoride

    International Nuclear Information System (INIS)

    1991-06-01

    Uranium hexafluoride (UF 6 ) is a radioactive material that has significant non-radiological hazardous properties. In conformity with international regulatory practice for dangerous goods transport, these properties are classed as ''subsidiary risks'', although they predominate in the cases of depleted and natural UF 6 . UF 6 is transported as a solid material below atmospheric pressure. The IAEA Regulations for the Safe Transport of Radioactive Material, 1985 Edition, Safety Series No. 6, make recommendations that aimed to provide an adequate level of safety against radiological and criticality hazards. The basis for these is that the stringency of package performance requirements, operational procedures and approval and administrative procedures is graded relative to the severity of the hazard. The cylinders used for transporting UF 6 are also used in the production, storage and use of the material and that the fraction of their life cycle in which transport is involved is small. Consideration must also be given to the large number of existing cylinders (estimated to be between 60,000 and 70,000). Specific recommendations provided for UF 6 transport, listed in Section II, are additional to the requirements of the Regulations. The intent of these additional recommendations is to restrict contamination and to provide protection to workers and to the general public against the chemical hazard possibly resulting from a severe accident involving the transport of UF 6 , and in addition against the consequences of explosive rupture of small bare cylinders of UF 6 . 20 refs, figs and tabs

  8. 49 CFR 173.477 - Approval of packagings containing greater than 0.1 kg of non-fissile or fissile-excepted uranium...

    Science.gov (United States)

    2010-10-01

    ... kg of non-fissile or fissile-excepted uranium hexafluoride. 173.477 Section 173.477 Transportation... non-fissile or fissile-excepted uranium hexafluoride. (a) Each offeror of a package containing more than 0.1 kg of uranium hexafluoride must maintain on file for at least one year after the latest...

  9. Uranium hexafluoride: A manual of good handling practices

    International Nuclear Information System (INIS)

    1991-10-01

    For many years, the US Department of Energy (DOE) and its predecessor agencies have shared with the nuclear industry their experience in the area of uranium hexafluoride (UF 6 ) shipping containers and handling procedures. The information contained in this manual updates information contained in earlier issues. It covers the essential aspects of UF 6 handling, cylinder filling and emptying, general principles of weighing and sampling, shipping, and the use of protective overpacks. The physical and chemical properties of UF 6 are also described and tabulated. The nuclear industry is responsible for furnishing its own shipping cylinders and suitable protective overpacks. A substantial effort has been made by the industry to standardize UF 6 cylinders, samples, and overpacks. The quality of feed materials is important to the safe and efficient operation of the enriching facilities, and the UF 6 product purity from the enriching facilities is equally important to the fuel fabricator, the utilities, the operators of research reactors, and other users. The requirements have been the impetus for an aggressive effort by DOE and its contractors to develop accurate techniques for sampling and for chemical and isotopic analysis. A quality control program is maintained within the DOE enriching facilities to ensure that the proper degree of accuracy and precision are obtained for all the required measurements. The procedures and systems described for safe handling of UF 6 presented in this document have been developed and evaluated in DOE facilities during more than 40 years of handling vast quantities of UF 6 . With proper consideration for its nuclear properties, UF 6 may be safely handled in essentially the same manner as any other corrosive and/or toxic chemical

  10. Depleted uranium processing and fluorine extraction

    International Nuclear Information System (INIS)

    Laflin, S.T.

    2010-01-01

    Since the beginning of the nuclear era, there has never been a commercial solution for the large quantities of depleted uranium hexafluoride generated from uranium enrichment. In the United States alone, there is already in excess of 1.6 billion pounds (730 million kilograms) of DUF_6 currently stored. INIS is constructing a commercial uranium processing and fluorine extraction facility. The INIS facility will convert depleted uranium hexafluoride and use it as feed material for the patented Fluorine Extraction Process to produce high purity fluoride gases and anhydrous hydrofluoric acid. The project will provide an environmentally friendly and commercially viable solution for DUF_6 tails management. (author)

  11. Uranium conversion

    International Nuclear Information System (INIS)

    Oliver, Lena; Peterson, Jenny; Wilhelmsen, Katarina

    2006-03-01

    FOI, has performed a study on uranium conversion processes that are of importance in the production of different uranium compounds in the nuclear industry. The same conversion processes are of interest both when production of nuclear fuel and production of fissile material for nuclear weapons are considered. Countries that have nuclear weapons ambitions, with the intention to produce highly enriched uranium for weapons purposes, need some degree of uranium conversion capability depending on the uranium feed material available. This report describes the processes that are needed from uranium mining and milling to the different conversion processes for converting uranium ore concentrate to uranium hexafluoride. Uranium hexafluoride is the uranium compound used in most enrichment facilities. The processes needed to produce uranium dioxide for use in nuclear fuel and the processes needed to convert different uranium compounds to uranium metal - the form of uranium that is used in a nuclear weapon - are also presented. The production of uranium ore concentrate from uranium ore is included since uranium ore concentrate is the feed material required for a uranium conversion facility. Both the chemistry and principles or the different uranium conversion processes and the equipment needed in the processes are described. Since most of the equipment that is used in a uranium conversion facility is similar to that used in conventional chemical industry, it is difficult to determine if certain equipment is considered for uranium conversion or not. However, the chemical conversion processes where UF 6 and UF 4 are present require equipment that is made of corrosion resistant material

  12. LIQUID METAL COMPOSITIONS CONTAINING URANIUM

    Science.gov (United States)

    Teitel, R.J.

    1959-04-21

    Liquid metal compositions containing a solid uranium compound dispersed therein is described. Uranium combines with tin to form the intermetallic compound USn/sub 3/. It has been found that this compound may be incorporated into a liquid bath containing bismuth and lead-bismuth components, if a relatively small percentage of tin is also included in the bath. The composition has a low thermal neutron cross section which makes it suitable for use in a liquid metal fueled nuclear reactor.

  13. HGSYSTEMUF6, Simulating Dispersion Due to Atmospheric Release of Uranium Hexafluoride (UF6)

    International Nuclear Information System (INIS)

    Hanna, G; Chang, J.C.; Zhang, J.X.; Bloom, S.G.; Goode, W.D. Jr; Lombardi, D.A.; Yambert, M.W.

    2001-01-01

    , for a given time step, the equations governing the processes of dispersion, chemical reaction, and thermodynamics can be solved sequentially and independently. Here, a Runge-Kutta solver is employed to solve the equations governing dispersion, a simple, first-order forward finite difference scheme is used to solve the rate equations for the consumption and production of reactants, while the proprietary nonlinear algebraic equation solver NAESOL, developed by Shell Research LTD. is used to solve equations governing thermodynamic balances of molar fraction, enthalpy and molar flow rate of HF. Conversely, for simulating downwind dispersion of a passive, ideal gas, the WAKE component employs equations based on advanced empirical formulations of wind tunnel data in conjunction with the standard gaussian plume model formation. 3 - Restriction on the complexity of the problem: HGSYSTEMUF6 is designed for a single user on a single personal computer. Array dimensions have been initially set to reflect realistic, limiting values. By modification of these limits the user may create executable versions of model files that are limited only by the hardware configuration of their machine. HGSYSTEMUF6 is designed specifically for the simulation of atmospheric releases of Uranium Hexafluoride and its reaction products. For other simulations which involve the dispersion of vapour from gas, liquid or two-phase releases including multi-component mixtures, HGSYSTEM, is available at no charge from the official shell Research LTD HGSYSTEM Web site: http://www.users.virtual-chester.com/hgsystem or email HGSystem at OPC.shell.com

  14. Study of the dry processing of uranium ores

    International Nuclear Information System (INIS)

    Guillet, H.

    1959-02-01

    A description is given of direct fluorination of pre-concentrated uranium ores in order to obtain the hexafluoride. After normal sulfuric acid treatment of the ore to eliminate silica, the uranium is precipitated by a load of lime to obtain: either impure calcium uranate of medium grade, or containing around 10% of uranium. This concentrate is dried in an inert atmosphere and then treated with a current of elementary fluorine. The uranium hexafluoride formed is condensed at the outlet of the reaction vessel and may be used either for reduction to tetrafluoride and the subsequent manufacture of uranium metal or as the initial product in a diffusion plant. (author) [fr

  15. Design and construction of a Type B overpack container for the safe transportation of enriched uranium hexafluoride

    International Nuclear Information System (INIS)

    Gablin, K.A.

    1976-01-01

    The Paducah Tiger is an overpack designed for the international shipment of ten-ton cylinders of uranium hexafluoride in enriched form above the level of low specific acitivity. This container is designed as a Type B Package and has undergone all the tests and analyses required for a U.S. Department of Transportation Permit No. 6553. The Paducah Tiger is currently being used to ship fuel material in the USA on both truck and rail modes of transportation. In many ways, the design resembles the Super Tigersup(R), but incorporates features such as ISO corners, quick opening fasteners, and interior shock isolators that provide a system approach to the high volume of fuel shipment required in the last half of the 20th century. (author)

  16. Refurbishment of uranium hexafluoride cylinder storage yards C-745-K, L, M, N, and P and construction of a new uranium hexafluoride cylinder storage yard (C-745-T) at the Paducah Gaseous Diffusion Plant, Paducah, Kentucky

    International Nuclear Information System (INIS)

    1996-07-01

    The Paducah Gaseous Diffusion Plant (PGDP) is a uranium enrichment facility owned by the US Department of Energy (DOE). A residual of the uranium enrichment process is depleted uranium hexafluoride (UF6). Depleted UF6, a solid at ambient temperature, is stored in 32,200 steel cylinders that hold a maximum of 14 tons each. Storage conditions are suboptimal and have resulted in accelerated corrosion of cylinders, increasing the potential for a release of hazardous substances. Consequently, the DOE is proposing refurbishment of certain existing yards and construction of a new storage yard. This environmental assessment (EA) evaluates the impacts of the proposed action and no action and considers alternate sites for the proposed new storage yard. The proposed action includes (1) renovating five existing cylinder yards; (2) constructing a new UF6 storage yard; handling and onsite transport of cylinders among existing yards to accommodate construction; and (4) after refurbishment and construction, restacking of cylinders to meet spacing and inspection requirements. Based on the results of the analysis reported in the EA, DOE has determined that the proposed action is not a major Federal action that would significantly affect the quality of the human environment within the context of the National Environmental Policy Act of 1969. Therefore, DOE is issuing a Finding of No Significant Impact. Additionally, it is reported in this EA that the loss of less than one acre of wetlands at the proposed project site would not be a significant adverse impact

  17. Refurbishment of uranium hexafluoride cylinder storage yards C-745-K, L, M, N, and P and construction of a new uranium hexafluoride cylinder storage yard (C-745-T) at the Paducah Gaseous Diffusion Plant, Paducah, Kentucky

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-07-01

    The Paducah Gaseous Diffusion Plant (PGDP) is a uranium enrichment facility owned by the US Department of Energy (DOE). A residual of the uranium enrichment process is depleted uranium hexafluoride (UF6). Depleted UF6, a solid at ambient temperature, is stored in 32,200 steel cylinders that hold a maximum of 14 tons each. Storage conditions are suboptimal and have resulted in accelerated corrosion of cylinders, increasing the potential for a release of hazardous substances. Consequently, the DOE is proposing refurbishment of certain existing yards and construction of a new storage yard. This environmental assessment (EA) evaluates the impacts of the proposed action and no action and considers alternate sites for the proposed new storage yard. The proposed action includes (1) renovating five existing cylinder yards; (2) constructing a new UF6 storage yard; handling and onsite transport of cylinders among existing yards to accommodate construction; and (4) after refurbishment and construction, restacking of cylinders to meet spacing and inspection requirements. Based on the results of the analysis reported in the EA, DOE has determined that the proposed action is not a major Federal action that would significantly affect the quality of the human environment within the context of the National Environmental Policy Act of 1969. Therefore, DOE is issuing a Finding of No Significant Impact. Additionally, it is reported in this EA that the loss of less than one acre of wetlands at the proposed project site would not be a significant adverse impact.

  18. Application of liquid-liquid extraction in uranium hydrometallurgy (Paper No. : V-1)

    Energy Technology Data Exchange (ETDEWEB)

    Murthy, T K.S.; Koppiker, K S

    1979-01-01

    Uranium recovery from the ores is carried out exclusively by hydrometallurgical techniques. The initial solubilisation of uranium is achieved by either sodium carbonate or sulphuric acid leaching, the latter being more common. Further purification and upgrading of uranium from the sulphate liquors is carried out by an ion-exchange process. Solid resin type anion exchangers or liquid ion-exchangers are employed. The processing of uranium liquors is, perhaps, the first major application of liquid-liquid extraction in metal recovery. Organophosphoric acids were initially used but later the long-chain aliphatic amines have superseded them. The amine extraction system has been widely studied and several variations are now known. Chloride, nitrate, carbonate or sulphate or acid stripping can be used for getting back the uranium into the aqueous phase. Combination of ion exchange (resin type) and solvent extraction processes called Eluex processes are developed for special applications. Studies have also been made of solvent extraction of uranium from leach pulps instead of clear liquors. Tributylphosphate has found wide application in the refining of uranium concentrates to meet the stringent needs of nuclear purity. liquid-liquid extraction is, perhaps, the only successful technique for the recovery of uranium, as by-product, from wet-process phosphoric acid. This has opened up a new source of uranium.

  19. New approach for safeguarding enriched uranium hexafluoride bulk transfers

    International Nuclear Information System (INIS)

    Doeher, L.W.; Pontius, P.E.; Whetstone, J.R.

    1978-01-01

    The unique concepts of American National Standard ANSI N15.18-1975 ''Mass Calibration Techniques for Nuclear Material Control'' are discussed in regard to the establishment and maintenance of control of mass measurement of Uranium Hexafluoride (UF 6 ) both within and between facilities. Emphasis is placed on the role of control of the measurements between facilities, and thus establish decision points for detection of measurement problems and making safeguards judgments. The unique concepts include the use of artifacts of UF 6 packaging cylinders, calibrated by a central authority, to introduce the mass unit into all of the industries' weighing processes. These are called Replicate Mass Standards (RMS). This feat is accomplished by comparing the RMS to each facility's In-House Standards (IHS), also artifacts, and thence the usage of these IHS to quantify the systematic and random errors of each UF 6 mass measurement process. A recent demonstration, which exchanged UF 6 cylinders between two facilities, who used ANSI N15.18-1975 concepts and procedures is discussed. The discussion includes methodology and treatment of data for use in detection of measurement and safeguards problems. The discussion incorporates the methodology for data treatment and judgments concerning (1) the common base, (2) measurement process off-sets, (3) measurement process precision, and (4) shipper-receiver bulk measurement differences. From the evidence gained in the demonstration, conclusions are reached as to the usefulness of the realistic criteria for detection of mass measurement problems upon acceptance of the concepts of ANSI N15.18-1975

  20. Recovery of valuable products in liquid effluents from uranium and thorium pilot units

    International Nuclear Information System (INIS)

    Jardim, E.A.; Abrao, A.

    1988-01-01

    IPEN-CNEN/SP has being very active in refining yellowcake to pure ammonium diuranate which is converted to uranium trioxide, uranium dioxide, uranium tetra- and hexafluoride in a sequential way. The technology of the thorium purification and its conversion to nuclear grade products has been a practice since several years as well. For both elements the major waste to be worked is the refinate from the solvent extraction column where uranium and thorium are purified via TBP-varsol in pulsed columns. In this paper the actual processing technology is reviewed with special emphasis on the recovery of valuable products, mainly nitric acid and ammonium nitrate. Distilled nitric acid and the final sulfuric acid as residue are recycle. Ammonium nitrate from the precipitation of uranium diuranate is of good quality, being radioactivity and uranium-free, and recommended to be applied as fertilizer. In conclusion the main effort is to maximise the recycle and reuse of the abovementioned chemicals. (author) [pt

  1. Reuse of ammonium fluoride generated in the uranium hexafluoride conversion; Reutilizacao do fluoreto de amonio gerado na reconversao do hexafluoreto de uranio

    Energy Technology Data Exchange (ETDEWEB)

    Silva Neto, J.B.; Carvalho, E.F. Urano de; Durazzo, M., E-mail: jbsneto@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Riella, H.G [Universidade Federal de Santa Catarina (UFSC), Florianopolis, SC (Brazil)

    2010-07-01

    The Nuclear Fuel Centre of IPEN / CNEN - SP develops and manufactures dispersion fuel with high uranium concentration to meet the demand of the IEA-R1 reactor and future research reactors planned to be constructed in Brazil. The fuel uses uranium silicide (U{sub 3}Si{sub 2}) dispersed in aluminum. For producing the fuel, the processes for uranium hexafluoride (UF{sub 6}) conversion consist in obtaining U{sub 3}Si{sub 2} and / or U{sub 3}O{sub 8} through the preparation of intermediate compounds, among them ammonium uranyl carbonate - AUC, ammonium diuranate - DUA and uranium tetrafluoride - UF{sub 4}. This work describes a procedure for preparing uranium tetrafluoride by a dry route using as raw material the filtrate generated when producing routinely ammonium uranyl carbonate. The filtrate consists primarily of a solution containing high concentrations of ammonium (NH{sub 4}{sup +}), fluoride (F{sup -}), carbonate (CO{sub 3}{sup --}) and low concentrations of uranium. The procedure is basically the recovery of NH{sub 4}F and uranium, as UF{sub 4}, through the crystallization of ammonium bifluoride (NH{sub 4}HF{sub 2}) and, in a later step, the addition of UO{sub 2}, occurring fluoridation and decomposition. The UF{sub 4} obtained is further diluted in the UF{sub 4} produced routinely at IPEN / CNEN-SP by a wet route process. (author)

  2. Standard test method for isotopic analysis of uranium hexafluoride by double standard single-collector gas mass spectrometer method

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2010-01-01

    1.1 This is a quantitative test method applicable to determining the mass percent of uranium isotopes in uranium hexafluoride (UF6) samples with 235U concentrations between 0.1 and 5.0 mass %. 1.2 This test method may be applicable for the entire range of 235U concentrations for which adequate standards are available. 1.3 This test method is for analysis by a gas magnetic sector mass spectrometer with a single collector using interpolation to determine the isotopic concentration of an unknown sample between two characterized UF6 standards. 1.4 This test method is to replace the existing test method currently published in Test Methods C761 and is used in the nuclear fuel cycle for UF6 isotopic analyses. 1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.6 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appro...

  3. Preparation of small uranium hexafluoride samples in view of mass spectrometry analysis; Preparation de petits echantillons d'hexafluorure d'uranium en vue d'analyse spectrometrique de masse

    Energy Technology Data Exchange (ETDEWEB)

    Severin, Michel

    1958-07-01

    We have studied the preparation of uranium hexafluoride for the determination of the isotopic ratio {sup 235}U/{sup 238}U by means of a mass spectrometer. UF{sub 6} should be produced from an amount of raw material (metallic uranium or oxide) that should not exceed 0,1 g. Our method has a good yield (we have studied the rate of transformation) and gives samples which present a content of impurities (HF and SiF{sub 4}) low enough to enable correct isotopic measurements. The method which seemed the best uses the cobalt trifluoride as a fluorining agent. It is now in current use in the laboratories of mass spectrometry. (author) [French] Nous avons etudie la preparation de l'hexafluorure d'uranium en vue de la determination au spectrometre de masse du rapport isotopique {sup 235}U/{sup 238}U. L'hexafluorure d'uranium devait etre produit a partir d'une quantite de matiere premiere (uranium metallique ou oxyde) ne devant pas exceder 0,1 g. Nous avons mis au point une methode de preparation presentant un rendement eleve (etude du taux de transformation) et donnant des echantillons dont le taux d'impuretes (HF et SiF{sub 4}) est suffisamment faible pour permettre des mesures isotopiques correctes. La methode ayant donne le plus de satisfaction utilise le trifluorure de cobalt comme agent fluorant. Ce procede est maintenant couramment employe dans les laboratoires de spectrometrie de masse. (auteur)

  4. Biological assessment of the effects of construction and operation of a depleted uranium hexafluoride conversion facility at the Paducah, Kentucky, site.

    Energy Technology Data Exchange (ETDEWEB)

    Van Lonkhuyzen, R.

    2005-09-09

    The U.S. Department of Energy (DOE) Depleted Uranium Hexafluoride (DUF{sub 6}) Management Program evaluated alternatives for managing its inventory of DUF{sub 6} and issued the ''Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted Uranium Hexafluoride'' (DUF{sub 6} PEIS) in April 1999 (DOE 1999). The DUF{sub 6} inventory is stored in cylinders at three DOE sites: Paducah, Kentucky; Portsmouth, Ohio; and East Tennessee Technology Park (ETTP), near Oak Ridge, Tennessee. In the Record of Decision for the DUF{sub 6} PEIS, DOE stated its decision to promptly convert the DUF6 inventory to a more stable chemical form. Subsequently, the U.S. Congress passed, and the President signed, the ''2002 Supplemental Appropriations Act for Further Recovery from and Response to Terrorist Attacks on the United States'' (Public Law No. 107-206). This law stipulated in part that, within 30 days of enactment, DOE must award a contract for the design, construction, and operation of a DUF{sub 6} conversion plant at the Department's Paducah, Kentucky, and Portsmouth, Ohio, sites, and for the shipment of DUF{sub 6} cylinders stored at ETTP to the Portsmouth site for conversion. This biological assessment (BA) has been prepared by DOE, pursuant to the National Environmental Policy Act of 1969 (NEPA) and the Endangered Species Act of 1974, to evaluate potential impacts to federally listed species from the construction and operation of a conversion facility at the DOE Paducah site.

  5. Uranium conversion; Urankonvertering

    Energy Technology Data Exchange (ETDEWEB)

    Oliver, Lena; Peterson, Jenny; Wilhelmsen, Katarina [Swedish Defence Research Agency (FOI), Stockholm (Sweden)

    2006-03-15

    FOI, has performed a study on uranium conversion processes that are of importance in the production of different uranium compounds in the nuclear industry. The same conversion processes are of interest both when production of nuclear fuel and production of fissile material for nuclear weapons are considered. Countries that have nuclear weapons ambitions, with the intention to produce highly enriched uranium for weapons purposes, need some degree of uranium conversion capability depending on the uranium feed material available. This report describes the processes that are needed from uranium mining and milling to the different conversion processes for converting uranium ore concentrate to uranium hexafluoride. Uranium hexafluoride is the uranium compound used in most enrichment facilities. The processes needed to produce uranium dioxide for use in nuclear fuel and the processes needed to convert different uranium compounds to uranium metal - the form of uranium that is used in a nuclear weapon - are also presented. The production of uranium ore concentrate from uranium ore is included since uranium ore concentrate is the feed material required for a uranium conversion facility. Both the chemistry and principles or the different uranium conversion processes and the equipment needed in the processes are described. Since most of the equipment that is used in a uranium conversion facility is similar to that used in conventional chemical industry, it is difficult to determine if certain equipment is considered for uranium conversion or not. However, the chemical conversion processes where UF{sub 6} and UF{sub 4} are present require equipment that is made of corrosion resistant material.

  6. Uranium refining in South Africa. The production of uranium trioxide, considering raw material properties and nuclear purity requirements

    International Nuclear Information System (INIS)

    Colborn, R.P.; Bayne, D.L.G.; Slabber, M.N.

    1980-01-01

    Conventional practice results in raw materials being delivered to the uranium refineries in a form more suitable for transportation than for processing, and therefore the refineries are required to treat these raw materials to produce an acceptable intermediate feed stock. During this treatment, it is advantageous to include a purification step to ensure that the feed stock is of the required purity for nuclear grade uranium hexafluoride production, and this usually results in ammonium diuranate slurries of the required quality being produced as the intermediate feed stock. All subsequent processing steps can therefore be standardized and are effectively independent of the origin of the raw materials. It is established practice in South Africa to transport uranium as an ammonium diuranate slurry from the various mines to the Nufcor central processing plant for UOC production, and therefore the process for the production of uranium hexafluoride in South Africa was designed to take cognizance of existing transport techniques and to accept ammonium diuranate slurries as the raw material. The South African refinery will be able to process these slurries directly to uranium trioxide. This paper discusses the conditions under which the various ammonium diuranate raw materials, exhibiting a wide range of properties, can be effectively processed to produce a uranium trioxide of acceptably consistent properties. Mention is also made of the uranium hexafluoride distillation process adopted

  7. Acute toxicity of the hydrolysis products of uranium hexafluoride (UF6) when inhaled by the rat and guinea pig. Final report

    International Nuclear Information System (INIS)

    Leach, L.J.; Gelein, R.M.; Panner, B.J.; Yulie, C.L.; Cox, C.C.; Balys, M.M.; Rolchigo, P.M.

    1984-04-01

    This report presents the experimental animal data base from which human health consequences may be predicted from exposures mimicing accidental discharges of uranium hexafluoride (UF 6 ) in the uranium industry. Rats or guinea pigs were exposed for two, five, or ten minutes duration to air having 0.44 g U/m 3 + 0.16 g HF/m 3 to 276.67 g U/m 3 + 94.07 g HF/m 3 . Survivors of each exposure were observed for 14 days for signs of U or HF intoxication. Selected animals were necropsied and samples of major organs were studied histopathologically. When enriched UF 6 (94 percent 235 U) was used, the urine and feces from each animal were measured daily for U content. Selected samples of urine were bioassayed in order to trace the course of renal injury during the two week postexposure period. 28 references, 51 figures, 23 tables

  8. Derived enriched uranium market

    International Nuclear Information System (INIS)

    Rutkowski, E.

    1996-01-01

    The potential impact on the uranium market of highly enriched uranium from nuclear weapons dismantling in the Russian Federation and the USA is analyzed. Uranium supply, conversion, and enrichment factors are outlined for each country; inventories are also listed. The enrichment component and conversion components are expected to cause little disruption to uranium markets. The uranium component of Russian derived enriched uranium hexafluoride is unresolved; US legislation places constraints on its introduction into the US market

  9. Final programmatic environmental impact statement for alternative strategies for the long-term management and use of depleted uranium hexafluoride. Volume 3: Responses to public comments

    International Nuclear Information System (INIS)

    1999-04-01

    This PEIS assesses the potential impacts of alternative management strategies for depleted uranium hexafluoride (UF 6 ) currently stored at three DOE sites: Paducah site near Paducah, Kentucky, Portsmouth site near Portsmouth, Ohio; and K-25 site on the Oak Ridge Reservation, Oak Ridge, Tennessee. The alternatives analyzed in the PEIS include no action, long-term storage as UF 6 , long-term storage as uranium oxide, use as uranium oxide, use as uranium metal, and disposal. DOE's preferred alternative is to begin conversion of the depleted UF 6 inventory as soon as possible, either to uranium oxide, uranium metal, or a combination of both, while allowing for use of as much of this inventory as possible. This volume of the Final PEIS contains the comments and DOE's responses to comments received during the comment period. Chapter 2 contains photocopies of written submissions received by DOE on the Draft PEIS; DOE's responses to those comments are listed in Chapter 3. Chapter 4 provides the oral comments received at the public hearings and DOE's responses. Chapter 5 provides indices to comments and responses arranged by commentor name and by comment number

  10. Standard test method for isotopic analysis of hydrolyzed uranium hexafluoride and uranyl nitrate solutions by thermal ionization mass spectrometry

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2005-01-01

    1.1 This method applies to the determination of isotopic composition in hydrolyzed nuclear grade uranium hexafluoride. It covers isotopic abundance of 235U between 0.1 and 5.0 % mass fraction, abundance of 234U between 0.0055 and 0.05 % mass fraction, and abundance of 236U between 0.0003 and 0.5 % mass fraction. This test method may be applicable to other isotopic abundance providing that corresponding standards are available. 1.2 This test method can apply to uranyl nitrate solutions. This can be achieved either by transforming the uranyl nitrate solution to a uranyl fluoride solution prior to the deposition on the filaments or directly by depositing the uranyl nitrate solution on the filaments. In the latter case, a calibration with uranyl nitrate standards must be performed. 1.3 This test method can also apply to other nuclear grade matrices (for example, uranium oxides) by providing a chemical transformation to uranyl fluoride or uranyl nitrate solution. 1.4 This standard does not purport to address al...

  11. Estimation of risks associated to land transport of uranium hexafluoride

    International Nuclear Information System (INIS)

    Pages, P.; Tomachevsky, E.

    1987-01-01

    The system analysed concerns the packaging 48Y containing about 12 tons of hexafluoride, 1000 tons/year are forecasted for 1990 on the 900 km road Pierrelatte-Le Havre (France). Probabilities are given by the accident file, container failure by impact or fire and sanitary consequences are analysed. Risk is evaluated and discussed [fr

  12. Manhattan Project Technical Series: The Chemistry of Uranium (I)

    International Nuclear Information System (INIS)

    Rabinowitch, E. I.; Katz, J. J.

    1947-01-01

    This constitutes Chapters 11 through 16, inclusive, of the Survey Volume on Uranium Chemistry prepared for the Manhattan Project Technical Series. Chapters are titled: Uranium Oxides, Sulfides, Selenides, and Tellurides; The Non-Volatile Fluorides of Uranium; Uranium Hexafluoride; Uranium-Chlorine Compounds; Bromides, Iodides, and Pseudo-Halides of Uranium; and Oxyhalides of Uranium.

  13. Manhattan Project Technical Series: The Chemistry of Uranium (I)

    Energy Technology Data Exchange (ETDEWEB)

    Rabinowitch, E. I. [Argonne National Lab. (ANL), Argonne, IL (United States); Katz, J. J. [Argonne National Lab. (ANL), Argonne, IL (United States)

    1947-03-10

    This constitutes Chapters 11 through 16, inclusive, of the Survey Volume on Uranium Chemistry prepared for the Manhattan Project Technical Series. Chapters are titled: Uranium Oxides, Sulfides, Selenides, and Tellurides; The Non-Volatile Fluorides of Uranium; Uranium Hexafluoride; Uranium-Chlorine Compounds; Bromides, Iodides, and Pseudo-Halides of Uranium; and Oxyhalides of Uranium.

  14. Safety criteria of uranium enrichment plants

    International Nuclear Information System (INIS)

    Nardocci, A.C.; Oliveira Neto, J.M. de

    1994-01-01

    The applicability of nuclear reactor safety criteria applied to uranium enrichment plants is discussed, and a new criterion based on the soluble uranium compounds and hexafluoride chemical toxicities is presented. (L.C.J.A.). 21 refs, 4 tabs

  15. Gas-phase thermal dissociation of uranium hexafluoride: Investigation by the technique of laser-powered homogeneous pyrolysis

    International Nuclear Information System (INIS)

    Bostick, W.D.; McCulla, W.H.; Trowbridge, L.D.

    1987-04-01

    In the gas-phase, uranium hexafluoride decomposes thermally in a quasi-unimolecular reaction to yield uranium pentafluoride and atomic fluorine. We have investigated this reaction using the relatively new technique of laser-powered homogeneous pyrolysis, in which a megawatt infrared laser is used to generate short pulses of high gas temperatures under strictly homogeneous conditions. In our investigation, SiF 4 is used as the sensitizer to absorb energy from a pulsed CO 2 laser and to transfer this energy by collisions with the reactant gas. Ethyl chloride is used as an external standard ''thermometer'' gas to permit estimation of the unimolecular reaction rate constants by a relative rate approach. When UF 6 is the reactant, CF 3 Cl is used as reagent to trap atomic fluorine reaction product, forming CF 4 as a stable indicator which is easily detected by infrared spectroscopy. Using these techniques, we estimate the UF 6 unimolecular reaction rate constant near the high-pressure limit. In the Appendix, we describe a computer program, written for the IBM PC, which predicts unimolecular rate constants based on the Rice-Ramsperger-Kassel theory. Parameterization of the theoretical model is discussed, and recommendations are made for ''appropriate'' input parameters for use in predicting the gas-phase unimolecular reaction rate for UF 6 as a function of temperature and gas composition and total pressure. 85 refs., 17 figs., 14 tabs

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

    International Nuclear Information System (INIS)

    Barlow, C.R.; Alderson, J.H.; Blue, S.C.; Boelens, R.A.; Conkel, M.E.; Dorning, R.E.; Ecklund, C.D.; Halicks, W.G.; Henson, H.M.; Newman, V.S.; Philpot, H.E.; Taylor, M.S.; Vournazos, J.P.; Pryor, W.A.; Ziehlke, K.T.

    1992-07-01

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

  17. Liquid-liquid extraction and separation studies of uranium(VI)

    International Nuclear Information System (INIS)

    Langade, A.D.; Shinde, V.M.

    1980-01-01

    Separation of uranium(VI) from iron(III), molybdenum(VI), vanadium(V), bismuth(III), zirconium(IV) and thorium(IV) is achieved by liquid-liquid extraction with 4-methyl-3-pentene-2-one (mesityl oxide; MeO) from sodium salicylate media (0.1M, pH 6.0). The extracted species is UO 2 (HO.C 6 H 4 COO) 2 .2MeO. A procedure for separating 50 μg of uranium from mg amounts of the other metals is described. (author)

  18. Liquid uranium contaimment in refractories metals

    International Nuclear Information System (INIS)

    Duarte, J.L.; Padilha, A.F.

    1982-01-01

    Tests were performed on metalic materials for liquid uranium containment up to 2100 0 C. The materials Nb, Mo, Ta and W in the form of crucibles were tested at 2100 0 C for one hour in the presence of flowing argon. After testing, the crucibles were etched using HCl and analysed by optical metallography and electron proble microanalysis. The results are discussed in terms of Berthoud equation and indicated that the solubility limit of the crucible material in uranium at the temperature controlls the crucible dissolution by liquid uranium. The various phases formed, the mechanism of dissolution and the possible material for future use are presented and discussed. (Author) [pt

  19. The uranium fuel cycle at IPEN - Energy and Nuclear Research Institute, SP, Brazil

    International Nuclear Information System (INIS)

    Abrao, Alcidio

    1994-09-01

    This paper summarizes the progress of research concerning the uranium fuel cycle set up at the IPEN, Sao Paulo, from the raw yellow-cake to the uranium hexafluoride. It covers the reconversion of the hexafluoride to ammonium uranyl tricarbonate and the manufacturing of the fuel elements for the swimming pool IEA-R1 reactor. This review extends the coverage of two pilot plants for uranium purification based upon ion exchange, one demonstration unity for the purification of uranyl nitrate by solvent extraction in pulsed columns, the unity of uranium tetrafluoride into moving bed reactors and a second one based upon the wet chemistry via uranium dioxide and aqueous hydrogen fluoride. The paper mentions the pilot plant for the preparation of uranium trioxide by the thermal decomposition of ammonium diuranate and a second unity by the thermal denitration of uranyl nitrate. The paper outlines the fluorine plant and the unity for the hexafluoride preparation, the unity for the conversion of the hexa to the ammonium uranyl tricarbonate and the fabrication of fuel elements for the IEA-R1 reactor. (author)

  20. Uniform deposition of uranium hexafluoride (UF6): Standardized mass deposits and controlled isotopic ratios using a thermal fluorination method.

    Science.gov (United States)

    McNamara, Bruce K; O'Hara, Matthew J; Casella, Andrew M; Carter, Jennifer C; Addleman, R Shane; MacFarlan, Paul J

    2016-07-01

    We report a convenient method for the generation of volatile uranium hexafluoride (UF6) from solid uranium oxides and other U compounds, followed by uniform deposition of low levels of UF6 onto sampling coupons. Under laminar flow conditions, UF6 is shown to interact with surfaces within a fixed reactor geometry to a highly predictable degree. We demonstrate the preparation of U deposits that range between approximately 0.01 and 500ngcm(-2). The data suggest the method can be extended to creating depositions at the sub-picogramcm(-2) level. The isotopic composition of the deposits can be customized by selection of the U source materials and we demonstrate a layering technique whereby two U solids, each with a different isotopic composition, are employed to form successive layers of UF6 on a surface. The result is an ultra-thin deposit that bears an isotopic signature that is a composite of the two U sources. The reported deposition method has direct application to the development of unique analytical standards for nuclear safeguards and forensics. Further, the method allows access to very low atomic or molecular coverages of surfaces. Copyright © 2016 Elsevier B.V. All rights reserved.

  1. Market for natural uranium conversion. Commercial aspect

    International Nuclear Information System (INIS)

    Durret, L.F.

    1986-01-01

    The main activity of COMURHEX is the conversion into uranium hexafluoride of uranium concentrates from mines and owned by electricity producers. Capacities of the 5 uranium converters in the Western World are compared. About 50% of COMUREX turnover is exported. Evolution of the market and of stockpile are reviewed [fr

  2. The multiphoton ionization of uranium hexafluoride

    International Nuclear Information System (INIS)

    Armstrong, D.P.

    1992-05-01

    Multiphoton ionization (MPI) time-of-flight mass spectroscopy and photoelectron spectroscopy studies of UF 6 have been conducted using focused light from the Nd:YAG laser fundamental (λ=1064 nm) and its harmonics (λ=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 x + fragment ions even at the lowest laser power densities at which signal could be detected. The laser power dependence of U 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 2+ ) intensity is much greater than that of the singly-charged uranium ion (U + ). For the case of the tunable dye laser experiments, the U 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 2+ ion and the absence or very small intensities of UF x + 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

  3. Removal of hydrogen fluoride from uranium plant emissions

    International Nuclear Information System (INIS)

    Ramani, M.P.S.

    1997-01-01

    Uranium production technology involves the use of hydrogen fluoride at various stages. It is used in the production of uranium tetrafluoride as well as for the production of fluorine for the conversion of tetrafluoride to hexafluoride in isotopic enrichment plants. The sources of HF pollution in the industry, besides accidental spillages and leakages, are the final off-gases from the UF 4 production process or from the hydrogen reduction of hexafluoride (where such process is adopted), venting of tanks and reactors containing HF, safety pressure rupture discs as well as dust collection and ventilation systems

  4. Liquid membrane process for uranium recovery

    International Nuclear Information System (INIS)

    Valint, P.L. Jr.

    1982-01-01

    An improved liquid membrane emulsion extraction process for recovering uranium from a WPPA feed solution containing uranyl cations wherein said feed is contacted with a water-in-oil emulsion which extracts and captures the uranium in the interior aqueous phase thereof, wherein the improvement comprises the presence of an alkane diphosphonic acid uranium complexing agent in the interior phase of the emulsion. This improvement results in greater extraction efficiency

  5. Uranium fluorides analysis. Titanium spectrophotometric determination

    International Nuclear Information System (INIS)

    Anon.

    Titanium determination in uranium hexafluoride in the range 0.7 to 100 microgrammes after transformation of uranium fluoride in sulfate. Titanium is separated by extraction with N-benzoylphenylhydroxylamine, reextracted by hydrochloric-hydrofluoric acid. The complex titanium-N-benzoylphenylhydroxylamine is extracted by chloroform. Spectrophotometric determination at 400 nm [fr

  6. Behaviour of uranium dioxide in liquid nitrogen tetraoxide

    International Nuclear Information System (INIS)

    Kobets, L.V.; Klavsut', G.N.; Dolgov, V.M.

    1983-01-01

    Interaction kinetics of uranium dioxide with liquid nitrogen tetroxide at 25-150 deg C has been studied. It is shown that in the temperature range studied NO[UO 2 (NO 3 ) 3 ] is the final product of the reaction. With the increase of specific surface of uranium dioxide and with the temperature increase the degree of oxide transformation increases. Uranium dioxide-liquid N 2 O 4 interaction proceeds in the diffusion region. Seeming activation energies and rate constants of the mentioned processes are calculated. Effect of nitrogen trioxide additions on transformation kinetics is considered

  7. Study of the dry processing of uranium ores; Etude des traitements de minerais d'uranium par voie seche

    Energy Technology Data Exchange (ETDEWEB)

    Guillet, H

    1959-02-01

    A description is given of direct fluorination of pre-concentrated uranium ores in order to obtain the hexafluoride. After normal sulfuric acid treatment of the ore to eliminate silica, the uranium is precipitated by a load of lime to obtain: either impure calcium uranate of medium grade, or containing around 10% of uranium. This concentrate is dried in an inert atmosphere and then treated with a current of elementary fluorine. The uranium hexafluoride formed is condensed at the outlet of the reaction vessel and may be used either for reduction to tetrafluoride and the subsequent manufacture of uranium metal or as the initial product in a diffusion plant. (author) [French] Il s'agit d'une description de fluoration directe de preconcentres de minerais d'uranium en vue d'obtention d'hexafluorure. Apres attaque sulfurique normale du minerai, afin d' eliminer la silice, l' uranium est precipite par un toit de chaux pour obtenir: ou uranate de chaux impur de titre moyen, ou uranium de la dizaine du pourcentage. Ce concentre seche en atmosphere inerte est soumis a un courant de fluor elementaire. L'hexafluorure d'uranium forme est condense a la sortie du reacteur et peut etre utilise soit apres reduction en tetrafluorure par l'elaboration d'uranium metal, soit comme produit de base dans le cadre d'une usine de diffusion. (auteur)

  8. The IAEA recommendations for providing protection during the transport of uranium hexafluoride

    International Nuclear Information System (INIS)

    Levin, I.; Wieser, K.

    1988-01-01

    The Regulations for the safe transport of radioactive materials, are the basis of national and international regulations concerning this subject throughout the world. These regulations require that subsidiary hazards associated with radioactive materials should also be considered. Other national and international regulations concerning the transport of dangerous materials consider that a radioactive material having other dangerous properties should be classified as class 7. Following this line and acting upon the recommendations of SAGSTRAM (Standing Advisory Committee on the Safe Transport of Radioactive Materials) that the Agency should take the lead in providing guidance to Member States with respect to UF 6 packaging and transport, the Agency convened two expert meetings during 1986 and 1987 in order to look into the special problems associated with the transport of uranium hexafluoride. The experts identified several areas in which additional safety measures should be considered if the transport of UF 6 is to have a non-radiological safety level consistent with that of its radiological risks. In this presentation the new recommendations are described. The main safety issues to be discussed are fire resistance, valve protection and compatibility with service and structural equipment. Another aspect of importance is the interface between the process and the transport phases, bearing in mind that the same containers are used in both. This paper also reveals how far the new recommendations concerning UF 6 have already been endorsed in the forthcoming European Transport Regulations (ADR/RID) together with the 1985 revised Edition of IAEA Safety Series No. 6

  9. Recovery and treatment of uranium from uranium-containing solution by liquid membrane emulsion technology

    International Nuclear Information System (INIS)

    Xia Liangshu; Zhou Yantong; Xiao Yiqun; Peng Anguo; Xiao Jingshui; Chen Wei

    2014-01-01

    The recovery and treatment of uranium from uranium-containing solution using liquid membrane emulsion (LME) technology were studied in this paper, which contained the best volume ratio of membrane materials, stirring speed during emulsion process, the conditions of extracting, such as temperature, pH, initial concentration of uranium. Moreover, the mechanism for extracting uranium was also discussed. The best experimental conditions of emulsifying were acquired. The volume fractions of P 204 and liquid paraffin are 0.1 and 0.05, the volume ratios of Span80 and sulphonated kerosene to P 204 are 0.06 and 0.79 respectively, stirring speed is controlled in 2 000 r/min, and the concentration of inner phase is 4 mol/L. The recovery rate of uranium is up to 99% through the LME extracted uranium for 0.5 h at pH 2.5 and room temperature when the initial concentration is less than 400 mg/L and the volume ratio is 5 between the uranium-containing waste water and LME. The calculation results of Gibbs free energy show that the reaction process is spontaneous. (authors)

  10. Studies on the fluorination of tri uranium octa oxide to Uranium tetrafluoride

    Energy Technology Data Exchange (ETDEWEB)

    Rofail, N H; Elfekey, S A [Nuclear chemistry department, hot laboratories centre, atomic energy authority, Cairo, (Egypt)

    1995-10-01

    Uranium tetrafluoride suitable for both uranium metal and hexafluoride preparations, was prepared by fluorination of U{sub 3} O{sub 8} with C F{sub 2} Cl{sub 2}. It was found that the oct oxide must have certain physical and chemical specifications to satisfy the specifications needed for subsequent operations. X-ray diffraction analysis, infra red investigations and chemical analysis confirm that the obtained uranium tetrafluoride contains more than 97% of U F{sub 4} with tap density equals to 3.5 g/cc. 3 FIGS., 2 TABS.

  11. Isotopic analysis of uranium hexafluoride highly enriched in U-235; Analyse isotopique de l'hexafluorure d'uranium fortement enrichi en U 235

    Energy Technology Data Exchange (ETDEWEB)

    Chaussy, L; Boyer, R [Commissariat a l' Energie Atomique, Pierrelatte (France). Centre d' Etudes Nucleaires

    1968-07-01

    Isotopic analysis of uranium in the form of the hexafluoride by mass-spectrometry gives gross results which are not very accurate. Using a linear interpolation method applied to two standards it is possible to correct for this inaccuracy as long as the isotopic concentrations are less than about 10 per cent in U-235. Above this level, the interpolations formula overestimates the results, especially if the enrichment of the analyzed samples is higher than 1.3 with respect to the standards. A formula is proposed for correcting the interpolation equation and for the extending its field of application to high values of the enrichment ({approx_equal}2) and of the concentration. It is shown that by using this correction the results obtained have an accuracy which depends practically only on that of the standards, taking into account the dispersion in the measurements. (authors) [French] L'analyse isotopique de l'uranium sous forme d'hexafluorure, par spectrometrie de masse, fournit des resultats bruts entaches d'inexactitude. Une methode d'interpolation lineaire entre deux etalons permet de corriger cette inexactitude, tant que les concentrations isotopiques sont inferieures a 10 pour cent en U-235 environ. Au-dessus de cette valeur, la formule d'interpolation surestime les resultats, notamment si l'enrichissement des echantillons analyses par rapport aux etalons est superieur a 1,3. On propose une formule de correction de l'equation d'interpolation qui etend son domaine d'application jusqu'a des valeurs elevees d'enrichissement ({approx_equal}2) et de concentration. On montre experimentalement que par cette correction, les resultats atteignent, a la precision des mesures, une exactitude qui ne depend pratiquement plus que de celles des etalons. (auteurs)

  12. Transformations of highly enriched uranium into metal or oxide

    International Nuclear Information System (INIS)

    Nollet, P.; Sarrat, P.

    1964-01-01

    The enriched uranium workshops in Cadarache have a double purpose on the one hand to convert uranium hexafluoride into metal or oxide, and on the other hand to recover the uranium contained in scrap materials produced in the different metallurgical transformations. The principles that have been adopted for the design and safety of these workshops are reported. The nuclear safety is based on the geometrical limitations of the processing vessels. To establish the processes and the technology of these workshops, many studies have been made since 1960, some of which have led to original achievements. The uranium hexafluoride of high isotopic enrichment is converted either by injection of the gas into ammonia or by an original process of direct hydrogen reduction to uranium tetrafluoride. The uranium contained m uranium-zirconium metal scrap can be recovered by combustion with hydrogen chloride followed treatment of the uranium chloride by fluorine in order to obtain the uranium in the hexafluoride state. Recovery of the uranium contained m various scrap materials is obtained by a conventional refining process combustion of metallic scrap, nitric acid dissolution of the oxide, solvent purification by tributyl phosphate, ammonium diuranate precipitation, calcining, reduction and hydro fluorination into uranium tetrafluoride, bomb reduction by calcium and slag treatment. Two separate workshops operate along these lines one takes care of the uranium with an isotopic enrichment of up to 3 p. 100, the other handles the high enrichments. The handling of each step of this process, bearing in mind the necessity for nuclear safety, has raised some special technological problems and has led to the conception of new apparatus, in particular the roasting furnace for metal turnings, the nitric acid dissolution unit, the continuous precipitator and ever safe filter and dryer for ammonium diuranate, the reduction and hydro fluorination furnace and the slag recovery apparatus These are

  13. Uranium price reporting systems

    International Nuclear Information System (INIS)

    1987-09-01

    This report describes the systems for uranium price reporting currently available to the uranium industry. The report restricts itself to prices for U 3 O 8 natural uranium concentrates. Most purchases of natural uranium by utilities, and sales by producers, are conducted in this form. The bulk of uranium in electricity generation is enriched before use, and is converted to uranium hexafluoride, UF 6 , prior to enrichment. Some uranium is traded as UF 6 or as enriched uranium, particularly in the 'secondary' market. Prices for UF 6 and enriched uranium are not considered directly in this report. However, where transactions in UF 6 influence the reported price of U 3 O 8 this influence is taken into account. Unless otherwise indicated, the terms uranium and natural uranium used here refer exclusively to U 3 O 8 . (author)

  14. Compilation of Requirements for Safe Handling of Fluorine and Fluorine-Containing Products of Uranium Hexafluoride Conversion

    Energy Technology Data Exchange (ETDEWEB)

    Ferrada, J.J.

    2000-04-03

    Public Law (PL) 105-204 requires the U.S. Department of Energy to develop a plan for inclusion in the fiscal year 2000 budget for conversion of the Department's stockpile of depleted uranium hexafluoride (DUF{sub 6}) to a more stable form over an extended period. The conversion process into a more stable form will produce fluorine compounds (e.g., elemental fluorine or hydrofluoric acid) that need to be handled safely. This document compiles the requirements necessary to handle these materials within health and safety standards, which may apply in order to ensure protection of the environment and the safety and health of workers and the public. Fluorine is a pale-yellow gas with a pungent, irritating odor. It is the most reactive nonmetal and will react vigorously with most oxidizable substances at room temperature, frequently with ignition. Fluorine is a severe irritant of the eyes, mucous membranes, skin, and lungs. In humans, the inhalation of high concentrations causes laryngeal spasm and broncospasms, followed by the delayed onset of pulmonary edema. At sublethal levels, severe local irritation and laryngeal spasm will preclude voluntary exposure to high concentrations, unless the individual is trapped or incapacitated. A blast of fluorine gas on the shaved skin of a rabbit causes a second degree burn. Lower concentrations cause severe burns of insidious onset, resulting in ulceration, similar to the effects produced by hydrogen fluoride. Hydrofluoric acid is a colorless, fuming liquid or gas with a pungent odor. It is soluble in water with release of heat. Ingestion of an estimated 1.5 grams produced sudden death without gross pathological damage. Repeated ingestion of small amounts resulted in moderately advanced hardening of the bones. Contact of skin with anhydrous liquid produces severe burns. Inhalation of AHA or aqueous hydrofluoric acid mist or vapors can cause severe respiratory tract irritation that may be fatal. Based on the extreme chemical

  15. Study of the dry processing of uranium ores; Etude des traitements de minerais d'uranium par voie seche

    Energy Technology Data Exchange (ETDEWEB)

    Guillet, H

    1959-02-01

    A description is given of direct fluorination of pre-concentrated uranium ores in order to obtain the hexafluoride. After normal sulfuric acid treatment of the ore to eliminate silica, the uranium is precipitated by a load of lime to obtain: either impure calcium uranate of medium grade, or containing around 10% of uranium. This concentrate is dried in an inert atmosphere and then treated with a current of elementary fluorine. The uranium hexafluoride formed is condensed at the outlet of the reaction vessel and may be used either for reduction to tetrafluoride and the subsequent manufacture of uranium metal or as the initial product in a diffusion plant. (author) [French] Il s'agit d'une description de fluoration directe de preconcentres de minerais d'uranium en vue d'obtention d'hexafluorure. Apres attaque sulfurique normale du minerai, afin d' eliminer la silice, l' uranium est precipite par un toit de chaux pour obtenir: ou uranate de chaux impur de titre moyen, ou uranium de la dizaine du pourcentage. Ce concentre seche en atmosphere inerte est soumis a un courant de fluor elementaire. L'hexafluorure d'uranium forme est condense a la sortie du reacteur et peut etre utilise soit apres reduction en tetrafluorure par l'elaboration d'uranium metal, soit comme produit de base dans le cadre d'une usine de diffusion. (auteur)

  16. Uranium,Radium and Iron Absorption from Liquid Waste Uranium Ore Processing by Zeolite

    International Nuclear Information System (INIS)

    Wismawati, T; Sorot sudiro, A; Herjati, T

    1998-01-01

    The aim of this work is to determine zeolites sorption capacity and the distribution coefficient of uranium, radium, and iron in zeolite-liquid waste system. Mineralogical composition of zeolite used in the experiment has been determine by examining the thin sections of zeolite grains under a microscope. Zeolite has ben activated by the dilute sulfuric acid or sodium hydroxide solution. The results show that the use of 0.25 N sodium hydroxide solution could be optimizing the zeolite for uranium and iron ions sorption and that of 0.1 N sulfuric acid solution is for radium sorption. The re-activation process has been carried out in three hours. Under such a condition, the sorption efficiency of zeolite to those ions have been known to be 45.85% for uranium, 96.63 % for iron and 87.80 % for radium. The distribution coefficients of uranium, radium and iron ion in zeolite-liquid waste system have been calculated 0.85, 7.02, and 28.65 ml/g respectively

  17. Obtain of uranium concentrates from fertil liquids

    International Nuclear Information System (INIS)

    Narvaez Castillo, W.A.

    1992-01-01

    This research tried to encounter the form to remove uranium from the rock in the best way, for that it was used different process like leaching, extraction, concentration and precipitation. To leach the mineral was chosen basic leaching, using a mixture of carbonate-sodium bicarbonate, this method is more adequated for the basic nature of the mineral. In extraction was used specific uranium ionic interchanges, so was chosen a tertiary amine like Alamina 336. The concentration phase is intimately binding with the extraction by ionic interchange, for the capability of resine's extraction to obtain concentrated liquids. When the liquids were obtained with high concentration of uranium in the same time were purified and then were precipitated, for that we employed a precipitant agent like: Sodium hydroxide, Amonium hydroxide, Magnesium hydroxide, Hydrogen peroxide and phosphates. With all concentrates we obtain the YELLOW CAKE

  18. A validation study of the intertran model for assessing risks of transportation accidents: Road transport of uranium hexafluoride

    International Nuclear Information System (INIS)

    Tomachevsky, E.G.; Ringot, C.; Pages, P.; Hubert, P.

    1985-06-01

    The INTERTRAN code was developed by the IAEA in order to provide member states with a simple and rapide method of assessing the risk involved in the transportation of radioactive materials and one which was applicable on a worldwide scale. Before being used, this code must be validated and the CEA thus compared the results obtained with the conventional risk assessment methods used by the CEPN with those derived from INTERTRAN. This paper gives the results of the studies made on the subject of road transportation of uranium hexafluoride in France. The conventional accident risk assessment method gave a figure of 8.84 x 10 -4 deaths/year, whereas INTERTRAN announces 1.78 x 10 -2 . To these figures should be added 3.38 x 10 -2 deaths/year, which is the intrinsic road risk, whatever the goods carried. In relation to conventional estimates, the INTERTRAN forecasts are five times lower for the U risk and twenty times higher for the HF risk. The chemical risk is indeed the most prevalent one in this case. Other comparisons are needed to validate this code

  19. Similarity of dependences of thermal conductivity and density of uranium and tungsten hexafluorides on desublimation conditions

    International Nuclear Information System (INIS)

    Barkov, V.A.

    1989-01-01

    Consideration is given to results of investigations of the dependence of thermal conductivity and density of UF 6 and WF 6 desublimates on volume content of hexafluoride in initial gaseous mixture. Similarity of these dependences, as well as the dependences of thermal conductivity of desublimates on their density was revealed. Generalized expressions, relating thermal conductivity and density of desublimates among each ofter and with volume content of hexafluoride in gaseous mixture were derived. Possibility of applying the generalized relations for calculation of thermal conductivity and density of other compounds of MeF 6 type under prescribed desublimation conclitions is shown. 15 refs.; 6 figs

  20. Method for monitoring stack gases for uranium activity

    International Nuclear Information System (INIS)

    Beverly, C.R.; Ernstberger, H.G.

    1988-01-01

    A method for sampling stack gases emanating from the purge cascade of a gaseous diffusion cascade system utilized to enrich uranium for determining the presence and extent of uranium in the stack gases in the form of gaseous uranium hexafluoride, is described comprising the steps of removing a side stream of gases from the stack gases, contacting the side stream of the stack gases with a stream of air sufficiently saturated with moisture for reacting with and converting any gaseous uranium hexafluroide contracted thereby in the side stream of stack gases to particulate uranyl fluoride. Thereafter contacting the side stream of stack gases containing the particulate uranyl fluoride with moving filter means for continuously intercepting and conveying the intercepted particulate uranyl fluoride away from the side stream of stack gases, and continually scanning the moving filter means with radiation monitoring means for sensing the presence and extent of particulate uranyl fluoride on the moving filter means which is indicative of the extent of particulate uranyl fluoride in the side stream of stack gases which in turn is indicative of the presence and extent of uranium hexafluoride in the stack gases

  1. Improved ionic model of liquid uranium dioxide

    NARCIS (Netherlands)

    Gryaznov, [No Value; Iosilevski, [No Value; Yakub, E; Fortov, [No Value; Hyland, GJ; Ronchi, C

    The paper presents a model for liquid uranium dioxide, obtained by improving a simplified ionic model, previously adopted to describe the equation of state of this substance [1]. A "chemical picture" is used for liquid UO2 of stoichiometric and non-stoichiometric composition. Several ionic species

  2. Uranium Extraction From Artificial Liquid Waste Using Continuous Extraction Liquid membrane Technique

    International Nuclear Information System (INIS)

    Rusdianasari; Buchari

    2002-01-01

    The continuous extraction of uranium from artificial liquid waste by emulsion liquid membrane was carried out using one stage mixer-settler. This emulsion liquid membrane containing di-2-ethylhexylphosphoric acid (D2EHPA) and tri-n-buthyl phosphate (TBP) as carrier were carried out using one stage mixer-settler. The optimum condition gave the ratio of emulsion velocity to the feed velocity 1:4 and steady state reached after five minutes. The optimum condition was obtained at the 90.91 % of uranium recovered from raffinate, using EDTA as the masking agent with concentration 5x10 - 2 M . The total concentration of carrier was 3% with ratio D2EHPA and TBP 3:1. The emulsion liquid membrane has high relative selectivity after steady state with separation factors were α U , N i= 115,43 and α U , Fe 328,55. The result of experiment showed that emulsion liquid membrane containing D2EHPA and TBP as carrier have good performance for continuous system

  3. Simple and Rapid Dual-Dispersive Liquid-Liquid Microextraction as an Innovative Extraction Method for Uranium in Real Water Samples Prior to the Determination of Uranium by a Spectrophotometric Technique.

    Science.gov (United States)

    Khan, Naeemullah; Tuzen, Mustafa; Kazi, Tasneem Gul

    2017-11-01

    An innovative, rapid, and simple dual-dispersive liquid-liquid microextraction (DDLL-ME) approach was used to extract uranium from real samples for the first time. The main objective of this study was to disperse extraction solvent by using an air-agitated syringe system to overcome matrix effects and avoid dispersion of hazardous dispersive organic solvents by using heat. The DDLL-ME method consisted of two dispersive liquid-liquid extraction steps with chloroform as the extracting solvent. Uranium formed complexes with 4-(2-thiazolylazo) resorcinol in the aqueous phase and was extracted in extracting solvent (chloroform) after the first dispersive liquid-liquid process. Uranium was then back-extracted in the acidic aqueous phase in a second dispersive liquid-liquid process. Finally, uranium was determined by a spectrophotometric detection technique. The variables that played a key role in the proposed method were studied and optimized. The LOD and sensitivity enhancement factor for uranium were found to be 0.60 µg/L and 45, respectively, under optimized conditions. Calibration graphs were found to be linear in the range of 5.0-600 µg/L. The RSD was 2.5%. Reliability of the proposed method was verified by analyzing certified reference material TM-28.3.

  4. Process for uranium separation and preparation of UO4.2NH3.2HF

    International Nuclear Information System (INIS)

    Dokuzoguz, H.Z.

    1976-01-01

    A process for treating the aqueous effluents that are produced in converting gaseous UF 6 (uranium hexafluoride) into solid UO 2 (uranium dioxide) by way of an intermediate (NH 4 ) 4 UO 2 (CO 3 ) 3 (''AUC'' Compound) is disclosed. These effluents, which contain large amounts of NH 4 + , CO 3 2- , F - , and a small amount of U are mixed with H 2 SO 4 (sulfuric acid) in order to expel CO 2 (carbon dioxide) and thereby reduce the carbonate concentration. The uranium is precipitated through treatment with H 2 O 2 (hydrogen peroxide) and the fluoride is easily recovered in the form of CaF 2 (calcium fluoride) by contacting the process liquid with CaO (calcium oxide). The presence of SO 4 2- (sulfate) in the process liquid during CaO contacting seems to prevent the development of a difficult-to-filter colloid. The process also provides for NH 3 recovery and recycling. Liquids discharged from the process, moreover, are essentially free of environmental pollutants. The waste treatment products, i.e., CO 2 , NH 3 , and U are economically recovered and recycled back into the UF 6 → UO 2 conversion process. The process, moreover, recovers the uranium as a precipitate in the second stage. This precipitate is a new inorganic chemical compound UO 4 .2NH 3 .2HF [uranyl peroxide-2-ammonia-2-(hydrogen fluoride)

  5. Some economic aspects of the low enriched uranium production

    International Nuclear Information System (INIS)

    1990-05-01

    At the Technical Committee Meeting on Economics of Low Enriched Uranium 14 papers were presented. A separate abstract was prepared for each of these papers. The five technical sessions covered several economic aspects of uranium concentrates production, conversion into uranium hexafluoride and uranium enrichment and the recycling of U and Pu in LWR. Four Panel discussions were held to discuss the uranium market trends, the situation of conversion industry, the reprocessing and the uranium market, the future trends of enrichment and the economics of LWRs compared with other reactors. Refs, figs and tabs

  6. Uranium extraction process in a sulfuric medium by means of liquid emulsified membranes

    International Nuclear Information System (INIS)

    Monteillet, A.

    1985-02-01

    Uranium ore processing, after leaching by sulfuric acid, by liquid-liquid extraction is a rather heavy process, not suitable for small deposits. Extraction by emulsions was suggested. In this process the leachate is contacted with an oil in water type emulsion, a liquid organic membrane is formed by the continuous phase. Uranium complexes diffuse through the liquid membrane towards the dispersed aqueous phase of the emulsion (stripping solution). Uranium is recovered by breaking the emulsion. Are successively studied: development of stable emulsions, influence of emulsion composition on uranium transfer kinetics, transfer mechanisms through the membrane and modelling of kinetics data obtained in the experimental study [fr

  7. The study on process of recycling uranium in mixture of residue and liquid

    International Nuclear Information System (INIS)

    Zhang Jie; Shen Weiwei; Hao Jidong; Wu Jiangming

    2014-01-01

    The treat method of mixture of residue and liquid produced from HWR nuclear fuel chemical process using some kind of U_3O_8 powder was studied in this experiment. For recycling the uranium in mixture of residue and liquid, chemical dissolving method, washing and centrifuging method and dilute nitric acid leaching uranium method was contrasted in this test. The merit of dilute nitric acid leaching uranium method is simpler, more effective and higher uranium recycling ratio. Next, dilute nitric acid leaching uranium method was studied systematically. As a result, the main influence factors of uranium recycling ratio is dip sour degree and dip sour temperature. The influence law of factors to uranium recycling ratio and filtering effect was found out also. Along with increasing of dip sour degree and dip sour temperature, uranium recycling ratio increases and speed of filtrate increases also. At last, the process of batch treating mixture of residue and liquid was build and abundant uranium was recycled. (authors)

  8. Liquid membranes and process for uranium recovery therewith

    International Nuclear Information System (INIS)

    Frankenfeld, J.W.; Li, N.N.T.; Bruncati, R.L.

    1981-01-01

    A liquid membrane system consisting of water-in-oil type emulsions dispersed in water, which is capable of extracting uranium-containing ions from an aqueous feed solution containing uranium ions at a temperature in the range of 25 0 C to 80 0 C, is described. The emulsion comprises an aqueous interior phase surrounded by a surfactant-containing exterior phase. The exterior phase is immiscible with the interior phase and comprises a transfer agent capable of transporting selectively the desired uranium-containing ions and a solvent for the transfer agent. The interior phase comprises a reactant capable of removing uranium-containing ions from the transfer agent and capable of changing the valency of the uranium in uranium-containing ions to a second valency state and converting the uranium-containing ions into a nonpermeable form. (U.K.)

  9. Options for disposal and reapplication of depleted uranium hexafluoride

    International Nuclear Information System (INIS)

    Fitch, St.H.

    2009-01-01

    The nuclear renaissance has spurred the need to enrich uranium to fuel power reactors to meet the nation's energy requirements. However, enriching uranium produces the volatile byproduct of DUF 6 tails. In an ambient environment, DUF 6 decomposes into uranium oxides and hydrogen fluoride (HF). This HF component makes DUF 6 unsuitable for disposal as low-level waste. To make DUF 6 suitable for disposal, it must be stabilized in a controlled process by converting it into uranium oxides and fluorine compounds by the processes of de-conversion and fluorine extraction. Once stabilized, the DU and fluorine have reapplication potential that would delay or divert the need for disposal. Certain challenges confound this process, notably the chemical toxicity from elemental fluorine and DU, radiation hazards, limited low-level waste disposal capacity, and potential political and public opposition. (authors)

  10. Uranium recovery from slags of metallic uranium

    International Nuclear Information System (INIS)

    Fornarolo, F.; Frajndlich, E.U.C.; Durazzo, M.

    2006-01-01

    The Center of the Nuclear Fuel of the Institute of Nuclear Energy Research - IPEN finished the program of attainment of fuel development for research reactors the base of Uranium Scilicet (U 3 Si 2 ) from Hexafluoride of Uranium (UF 6 ) with enrichment 20% in weight of 235 U. In the process of attainment of the league of U 3 Si 2 we have as Uranium intermediate product the metallic one whose attainment generates a slag contend Uranium. The present work shows the results gotten in the process of recovery of Uranium in slags of calcined slags of Uranium metallic. Uranium the metallic one is unstable, pyrophoricity and extremely reactive, whereas the U 3 O 8 is a steady oxide of low chemical reactivity, what it justifies the process of calcination of slags of Uranium metallic. The calcination of the Uranium slag of the metallic one in oxygen presence reduces Uranium metallic the U 3 O 8 . Experiments had been developed varying it of acid for Uranium control and excess, nitric molar concentration gram with regard to the stoichiometric leaching reaction of temperature of the leaching process. The 96,0% income proves the viability of the recovery process of slags of Uranium metallic, adopting it previous calcination of these slags in nitric way with low acid concentration and low temperature of leaching. (author)

  11. Depleted uranium management alternatives

    Energy Technology Data Exchange (ETDEWEB)

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

    1994-08-01

    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.

  12. Depleted uranium management alternatives

    International Nuclear Information System (INIS)

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

    1994-08-01

    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

  13. Treatment of liquid wastes from uranium hydrometallurgy

    International Nuclear Information System (INIS)

    Moraga G, J.C.

    1988-01-01

    Different treatments for low activity liquid wastes, generated by the hidromettalurgy of uranium ore are studied. A process of treatment was chosen which includes a neutralization with lime and limestone and a selective removal of Ra-226, through ion-exchange resins. A plant, with a capacity of treatment of 1 m 3 /h of liquid effluents was scoped. (author)

  14. No fluorinated compounds in the uranium conversion process: risk analysis and proposition of pictograms

    International Nuclear Information System (INIS)

    Jeronimo, Adroaldo Clovis; Oliveira, Wagner dos Santos

    2012-01-01

    The plants comprising the chemical conversion of uranium, which are part of the nuclear fuel cycle, present some risks, among others, because are associated with the non-fluorinated compounds handled in these processes. This study is the analysis of the risks associated with these compounds, i e, the non-fluorinated reactants and products, handled in different chemical processing plants, which include the production of uranium hexafluoride, while emphasizing the responsibilities and actions that fit to the chemical engineer with regard to minimizing risks during the various stages. The work is based on the experience gained during the development and mastery of the technology of production of uranium hexafluoride, the IPEN/ CNEN-SP, during the '80s, with the support of COPESP -Navy of Brazil. (author)

  15. Liquid-liquid extraction of uranium (VI) using Cyanex 272 in kerosene from sodium salicylate medium

    International Nuclear Information System (INIS)

    Kamble, Pravin N.; Mohite, Baburao S.; Suryavanshi, Vishal J.; Salunkhe, Suresh T.

    2015-01-01

    Liquid-liquid extraction of uranium (VI) from sodium salicylate media using Cyanex 272 in kerosene has been carried out. Uranium (VI) was quantitatively extracted from 1x10 -4 M sodium salicylate with 5x10 -4 M Cyanex 272 in kerosene. It was stripped quantitatively from the organic phase with 4M HCl and determined spectrophotometrically with arsenazo(III) at 600 nm. The effects of concentrations of sodium salicylate, metal ions and strippants have been studied. Separation of uranium (VI) from other elements was achieved from binary as well as from multicomponent mixtures. The method is simple, rapid and selective with good reproducibility (approximately ±2%). (author)

  16. Development of an On-Line Uranium Enrichment Monitor

    International Nuclear Information System (INIS)

    Xuesheng, L.; Guorong, L.; Yonggang, Z.; Xueyuan, H. X.-Y.

    2015-01-01

    An on-line enrichment monitor was developed to measure the enrichment of UF6 flowing through the processing pipes in centrifuge uranium enrichment plant. A NaI(Tl) detector was used to measure the count rates of the 186 keV gamma ray emitted from 235U, and the total quantity of uranium was determined from thermodynamic characteristics of gaseous uranium hexafluoride. The results show that the maximum relative standard deviation is less than 1% when the measurement time is 120 s or more and the pressure is more than 2 kPa in the measurement chamber. There are two working models for the monitor. The monitor works normally in the continuous model, When the gas's pressure in the pipe fluctuates greatly, it can work in the intermittent model, and the measurement result is very well. The background of the monitor can be measured automatically periodically. It can control automatically electromagnetic valves open and close, so as to change the gas's quantity in the chamber. It is a kind of unattended and remote monitor, all of data can be transfer to central control room. It should be effective for nuclear materials accountability verifications and materials balance verification at uranium enrichment plant by using the monitor to monitor Uranium enrichment of gaseous uranium hexafluoride in the output end of cascade continuously. (author)

  17. Determination of uranium in liquid samples

    International Nuclear Information System (INIS)

    Macefat, Martina R.; Grahek, Zeljko; Ivsic, Astrid G.

    2008-01-01

    Full text: Uranium is a natural occurring radionuclide and the first member of natural radioactive chains which makes its determination in natural materials interesting from geochemical and radioecological aspect. It can be quantitatively determined as element and/or its radioisotopes by different spectrometric methods (ICP-MS, spectrophotometry, alpha spectrometry). It is necessary to develop inexpensive, rapid and sensitive methods for the routine analysis. Therefore, in this paper, development of a new method for the isolation of uranium from liquid samples and subsequent determination by spectrophotometry and ICP-MS will be described. It is possible to isolate uranium from drinking and seawater using extraction chromatography or mixed solvent ion exchange. Uranium can be strongly bound on the TRU extraction chromatographic resin from nitric acid (chemical recovery is 100%) and can be separated from other interfering elements, while separation from thorium, which can be also strongly bound on this resin, is possible with hydrochloric acid. It is also possible to separate uranium from thorium on the anion exchanger Amberlite CG-400 (NO 3 - form) because uranium is much more weakly bound on this exchanger from alcoholic solutions of nitric acid. After the separation uranium is determined by ICP-MS and by spectrophotometric method with arsenazo III (λ max =652 nm). Developed method enables selection of the optimal mode of isolation for the given purposes. (author)

  18. Joint ANSI-INMM 8.1: Nuclear Regulatory Commission study of uranium hexafluoride cylinder material accountability bulk measurements

    International Nuclear Information System (INIS)

    Pontius, P.E.; Doher, L.W.

    1977-01-01

    This paper reports the progress to date in a demonstration of the procedures in ANSI N15.18-1975, ''Mass Calibration Techniques for Nuclear Material Control,'' sponsored and funded by the Nuclear Regulatory Commission (NRC). The philosophy of mass measurement as a production process, as promulgated in ANSI N15.18-1975, is reviewed. Special emphasis is placed on the use of artifact Reference Mass Standards (RMS) as references for uranium hexafluoride (UF 6 ) calibration and bulk measurement processes. The history of the creation of the artifact concept and its adoption by ANSI N15.18-1975 and the Nuclear Regulatory Commission is narrated. The program now under way is specifically described; including descriptions of the RMS, their calibration, and the assignment of uncertainties to them by the National Bureau of Standards (NBS). Instrument tests, in-house standards (IHS), and assignment of values relative to the RMS-NBS values at nuclear facilities which measure UF 6 cylinders are described. Comparisons and the data base are detailed to provide realistic measurement process parameters associated with accountable transfer of UF 6 . The as yet uncompleted part of the demonstration is described, that is, to further close the measurement loop by verification both between and within facilities

  19. Method of decontamination for uranium oxide particles floating in liquid waste

    International Nuclear Information System (INIS)

    Terakado, Tsutomu; Ebara, Tsuneo; Sato, Kuniaki.

    1981-01-01

    Purpose: To rapidly treat liquid waste containing uranium oxide particles floating in it and to enable substantially complete decontamination. Method: An iron salt such as ferrous sulfate or the like is added to liquid waste with floating uranium oxide particles, an alkaline solution such as caustic soda or the like is then added to the liquid waste while feeding compressed air at 0.1 to 0.02 l/sec. per ton of liquid waste, and the pH of the liquid waste is made to from 6.5 to 7.5. Thereafter, the feed of compressed air is stopped, the liquid waste is allowed to stand, and is then filtered. (Aizawa, K.)

  20. Pre-concentration of uranium from water samples by dispersive liquid-liquid micro-extraction

    Energy Technology Data Exchange (ETDEWEB)

    Khajeh, Mostafa; Nemch, Tabandeh Karimi [Zabol Univ. (Iran, Islamic Republic of). Dept. of Chemistry

    2014-07-01

    In this study, a simple and rapid dispersive liquid-liquid microextraction (DLLME) was developed for the determination of uranium in water samples prior to high performance liquid chromatography with diode array detection. 1-(2-pyridylazo)-2-naphthol (PAN) was used as complexing agent. The effect of various parameters on the extraction step including type and volume of extraction and dispersive solvents, pH of solution, concentration of PAN, extraction time, sample volume and ionic strength were studied and optimized. Under the optimum conditions, the limit of detection (LOD) and preconcentration factor were 0.3 μg L{sup -1} and 194, respectively. Furthermore, the relative standard deviation of the ten replicate was <2.6%. The developed procedure was then applied to the extraction and determination of uranium in the water samples.

  1. Pre-concentration of uranium from water samples by dispersive liquid-liquid micro-extraction

    International Nuclear Information System (INIS)

    Khajeh, Mostafa; Nemch, Tabandeh Karimi

    2014-01-01

    In this study, a simple and rapid dispersive liquid-liquid microextraction (DLLME) was developed for the determination of uranium in water samples prior to high performance liquid chromatography with diode array detection. 1-(2-pyridylazo)-2-naphthol (PAN) was used as complexing agent. The effect of various parameters on the extraction step including type and volume of extraction and dispersive solvents, pH of solution, concentration of PAN, extraction time, sample volume and ionic strength were studied and optimized. Under the optimum conditions, the limit of detection (LOD) and preconcentration factor were 0.3 μg L -1 and 194, respectively. Furthermore, the relative standard deviation of the ten replicate was <2.6%. The developed procedure was then applied to the extraction and determination of uranium in the water samples.

  2. On the technical development to minimize the quantity of solid wastes in a uranium conversion

    International Nuclear Information System (INIS)

    Otomura, Keiichiro; Ogura, Yoshikazu; Fujisaki, Sakae

    1987-01-01

    We have developed the new process of treating the waste liquor from a uranium conversion at Ningyo Toge Works PNC, Japan. This process consists of neutralizing precipitation, solid liquid separation, distillation and adsorption. At a neutralizing precipitation step a magnesium oxide is added in the waste liquor containing uranium and fluorine. Most of the uranium and fluorine in the waste liquor precipitate as magnesium compounds. A sulfuric acid is added to the precipitate separated by a filter to dissolve. The resulting solution is then distilled to recover a hydrofluoric acid as a distillate. Uranium is recovered from a residue by an anion exchange method. The recoverd fluorine and uranium are recycled to the main process of conversion. The filtrate separated at the precipitation step is then passed through adsorbing columns. The residual fluorine and uranium in the filtrate were adsorbed and removed by the chelating resine which selectively adsorb the uranium and fluorine. After that the treated waste liquor is discharged out of the plant. This process has merits of being able to minimize the quantity of solid waste in comparison with the conventional process and to recover uranium and fluorine. This process can also be applied to uranium reconversion process from uranium hexafluoride to uranium oxide and to uranium metal production process, which produce the same kind of waste liquor. (author)

  3. FIREPLUME model for plume dispersion from fires: Application to uranium hexafluoride cylinder fires

    International Nuclear Information System (INIS)

    Brown, D.F.; Dunn, W.E.

    1997-06-01

    This report provides basic documentation of the FIREPLUME model and discusses its application to the prediction of health impacts resulting from releases of uranium hexafluoride (UF 6 ) in fires. The model application outlined in this report was conducted for the Draft Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted UF 6 . The FIREPLUME model is an advanced stochastic model for atmospheric plume dispersion that predicts the downwind consequences of a release of toxic materials from an explosion or a fire. The model is based on the nonbuoyant atmospheric dispersion model MCLDM (Monte Carlo Lagrangian Dispersion Model), which has been shown to be consistent with available laboratory and field data. The inclusion of buoyancy and the addition of a postprocessor to evaluate time-varying concentrations lead to the current model. The FIREPLUME model, as applied to fire-related UF 6 cylinder releases, accounts for three phases of release and dispersion. The first phase of release involves the hydraulic rupture of the cylinder due to heating of the UF 6 in the fire. The second phase involves the emission of material into the burning fire, and the third phase involves the emission of material after the fire has died during the cool-down period. The model predicts the downwind concentration of the material as a function of time at any point downwind at or above the ground. All together, five fire-related release scenarios are examined in this report. For each scenario, downwind concentrations of the UF 6 reaction products, uranyl fluoride and hydrogen fluoride, are provided for two meteorological conditions: (1) D stability with a 4-m/s wind speed, and (2) F stability with a 1-m/s wind speed

  4. Uranium recovering from slags generated in the metallic uranium by magnesiothermic reduction

    International Nuclear Information System (INIS)

    Fornarolo, F.; Carvalho, E.F. Urano de; Durazzo, M.; Riella, H.G.

    2008-01-01

    The Nuclear Fuel Center of IPEN/CNEN-SP has recent/y concluded a program for developing the fabrication technology of the nuclear fuel based on the U 3 Si 2 -Al dispersion, which is being used in the IEA-R1 research reactor. The uranium silicide (U 3 Si 2 ) fuel production starts with the uranium hexafluoride (UF 6 ) processing and uranium tetrafluoride (UF 4 ) precipitation. Then, the UF 4 is converted to metallic uranium by magnesiothermic reduction. The UF 4 reduction by magnesium generates MgF 2 slag containing considerable concentrations of uranium, which could reach 20 wt%. The uranium contained in that slag should be recovered and this work presents the results obtained in recovering the uranium from that slag. The uranium recovery is accomplished by acidic leaching of the calcined slag. The calcination transforms the metallic uranium in U 3 O 8 , promoting the pulverization of the pieces of metallic uranium and facilitating the leaching operation. As process variables, have been considered the nitric molar concentration, the acid excess regarding the stoichiometry and the leaching temperature. As result, the uranium recovery reached a 96% yield. (author)

  5. Minimum critical masses for uranium at the Portsmouth Gaseous Diffusion Plant

    International Nuclear Information System (INIS)

    Tayloe, R.W. Jr.; Davis, T.C.

    1994-06-01

    This report presents a tabulation of safe masses and minimum critical masses for uranium (U). These minimum critical mass and safe mass tables were obtained by interpolating between the values reported in the literature to obtain values as a function of enrichment within the 1.5 percent to 100 percent range. Equivalent mass values for uranium-235 (U 235 ), uranium hexafluoride (UF 6 ), and uranyl fluoride (UO 2 F 2 ) have been generated from the safe mass and minimum critical masses for uranium

  6. Relationship of pressure to temperature rise in overfilled cylinders

    International Nuclear Information System (INIS)

    Barber, E.J.

    1979-01-01

    Mild steel pressure vessels containing uranium hexafluoride are heated in 96-inch diameter autoclaves to allow the feed material to enter the gaseous diffusion process equipment for enrichment in the uranium 235 isotope. For purposes of safety analysis it is necessary to establish the ability of the instrumentation to shut off the steam supply to the autoclave prior to cylinder rupture if the cylinder has been overfilled. To make this determination requires estimates of the rate of change of pressure with respect to change of temperature at constant volume as a function of the temperature at which the ullage disappears. The paper presents the calculations for the estimation of this rate of change for liquid uranium hexafluoride using the ratio of the coefficients of expansion and compressibility using empirical liquid density data and the Eyring equation of state for liquids. 5 figs. (MB)

  7. Uranium - the element: its occurrence and uses

    International Nuclear Information System (INIS)

    Awan, I. Z.

    2015-01-01

    Uranium metal and its compounds have been of great interest to physicists and chemists due to its use for both civil and military applications, e.g. production of electricity, use in the medical field and for making nuclear weapons. This review paper describes the occurrence, chemistry and metallurgy of the element 'uranium', its conversion to stable compounds such as yellow cake, uranium tetrafluoride and uranium hexafluoride and the enrichment technologies and uses for both civil and military purposes. The paper is meant for ready reference for students and teachers in connection with the recent spate of interest shown in nuclear power generation in Pakistan and abroad. (author)

  8. Liquid-liquid extraction of uranium(VI) using Cyanex 272 in toluene from sodium salicylate medium

    International Nuclear Information System (INIS)

    Madane, Namdev S.; Nikam, Gurunath H.; Jadhav, Deepali V.; Mohite, Baburao S.

    2011-01-01

    Liquid-liquid extraction of U(VI) from sodium salicylate media using Cyanex 272 in toluene has been carried out. Uranium(VI) was quantitatively extracted from 1 x 10 -3 M sodium salicylate with 5 x 10 -4 M Cyanex 272 in toluene. It was stripped quantitatively from the organic phase with 1M HCl and determined spectrophotometrically with arsenazo(III) at 660 nm. The effect of concentrations of sodium salicylate, extractant, diluents, metal ion and strippants have been studied. Separation of uranium(VI) from other elements was achieved from binary as well as from multicomponent mixtures. The method was extended to determination of uranium(VI) in geological samples. The method is simple, rapid and selective with good reproducibility (approximately ± 2%). (author)

  9. Microbial accumulation of uranium from nuclear liquid waste

    International Nuclear Information System (INIS)

    Mahmood, A.H.

    1986-01-01

    This investigation includes the isolation, identification and the fluctuations of the population densities of microorganisms in the nuclear liquid waste released by some laboratories of Iraqi Atomic Energy Commission. The efficiency of uranium accumulation on isolates (22 bacterial strains, 24 fungal strains and 6 yeast strains) was assessed in aqueous solution using fluorometric techniques. Two of the isolated microoganisms namely Bacillus sp. -15B and Mucor sp.16F showed exceptionally high attitude towards uranium accumulation. Optimal conditions required for efficient accumulation and recovery of uranium was then studied using the two selected isolates. 10 figs.; 162 refs.; 16 tabs

  10. Process of quantity determination of uranium by chromatography in liquid zone

    International Nuclear Information System (INIS)

    Muller, J.P.; Cojean, J.; Daubizit, M.

    1993-01-01

    The invention concerns a process of quantity determination of uranium by chromatography in liquid zone, usable to determine the quantity of uranium traces. Solutions to be treated can be aqueous or organic

  11. Chemical treatment of ammonium fluoride solution in uranium reconversion plant

    International Nuclear Information System (INIS)

    Carvalho Frajndlich, E.U. de.

    1992-01-01

    A chemical procedure is described for the treatment of the filtrate, produced from the transformation of uranium hexafluoride (U F 6 ) into ammonium uranyl carbonate (AUC). This filtrate is an intermediate product in the U F 6 to uranium dioxide (U O 2 ) reconversion process. The described procedure recovers uranium as ammonium peroxide fluoro uranate (APOFU) by precipitation with hydrogen peroxide (H 2 O 2 ), and as later step, its calcium fluoride (CaF 2 ) co-precipitation. The recovered uranium is recycled to the AUC production plant. (author)

  12. Contribution to Yttria corrosion study by liquid uranium

    International Nuclear Information System (INIS)

    Tournier, C.

    1995-02-01

    We are studying liquid uranium and polycrystalline Yttria interactions under secondary vacuum. The type, morphology and thickness of interfacial reaction products between U and Y 2 O 3 are examined by optical and confocal microscopy, SEM, X ray diffraction, X analysis and XPS. The most important parameters are the stoechiometry and microstructure of the Yttria, the oxygen partial pressure of the furnace atmosphere, pO 2 , and the duration and temperature of experiments. In the thermodynamic modelization, we take into account exchanges at the ceramic/metal interface and exchanges between the molten metal and the furnace atmosphere. Liquid uranium reacts with Yttria to form UO 2 at the interface which gradually changes into a solid solution UO 2 -Y 2 O 3 . The total thickness of reaction products results from two opposing reactions: (i) oxidation of uranium by Yttria (low pO 2 ) or by the atmosphere (high pO 2 ), controlled by migration of oxygen vacancies at Yttria grain boundaries. (ii) deoxidation caused by the formation of volatile uranium monoxide. On the other hand, we observed a transition of the type ''non-wettability → wettability '' which occurs subsequent to an increase of the stoichiometric variation x in Y 2 O 3-x . (author). 69 refs., 76 figs., 30 tabs

  13. The uncertainty evaluation of measurement for uranium in UF_6 hydrolysate by potentiometric titration

    International Nuclear Information System (INIS)

    Jiang Haiying; Cheng Ruoyu; Meng Xiujun

    2014-01-01

    Based on the building of mathematical model, this paper analyzed the origin of component of indeterminacy of which the measurement result for uranium in uranium hexafluoride hydrolysate by potentiometric titration, also each uncertainty was calculated and the expanded uncertainty was given. By evaluation the result of the uranium concentration is that: (158.88 + 1.22) mgU/mL, K = 2, P = 95%. (authors)

  14. Can ionic liquids be used as templating agents for controlled design of uranium-containing nanomaterials?

    International Nuclear Information System (INIS)

    Visser, Ann E.; Bridges, Nicholas J.; Tosten, Michael H.

    2013-01-01

    Graphical abstract: - Highlights: • Uranium oxides nanoparticles prepared using ionic liquids. • IL cation alkyl length impacts oxide morphology. • Low temperature UO 2 synthesis. - Abstract: Nanostructured uranium oxides have been prepared in ionic liquids as templating agents. Using the ionic liquids as reaction media for inorganic nanomaterials takes advantage of the pre-organized structure of the ionic liquids which in turn controls the morphology of the inorganic nanomaterials. Variation of ionic liquid cation structure was investigated to determine the impact on the uranium oxide morphologies. For two ionic liquid cations, increasing the alkyl chain length increases the aspect ratio of the resulting nanostructured oxides. Understanding the resulting metal oxide morphologies could enhance fuel stability and design

  15. Development of uranium milling and conversion

    International Nuclear Information System (INIS)

    Takada, Shingo; Hirono, Shuichiro.

    1983-11-01

    The development and improvement of uranium milling and refining producing uranium tetrafluoride from ores by the wet process, without producing yellowcake as an intermediate product, have been carried out for over ten years with a small pilot plant (50 t-ore/day). In the past several years, a process for converting uranium tetrafluoride into hexafluoride has been developed successfully. To develop the process further, the construction of an integrated milling and conversion pilot plant (200 t-U/year) started in 1979 and was completed in 1981. This new plant has two systems of solvent extraction using tri-noctylamine: one of the systems treats the pregnant solution (uranyl sulphate) by heap-leaching followed by ion exchange, and the other treats the uranyl sulphate solution by dissolving imported yellowcake. The uranium loading solvents from the two systems are stripped with hydrochloric acid solution to obtain the concentrated uranium solution containing 100 g-U/1. Uranyl sulphate solution from the stripping circuit is reduced to a uranous sulphate solution by the electrolytic method. In a reduction cell, uranyl sulphate solution and dilute sulphuric acid are used respectively as catholyte and anolyte, and a cation exchange membrane is used to prevent re-oxidation of the uranous sulphate. In the following hydrofluorination step, uranium tetrafluoride, UF 4 .1-1.2H 2 O (particle size: 50-100μ), is produced continuously as the precipitate in an improved reaction vessel, and this makes it possible to simplify the procedures of liquid-solid separation, drying and granulation. The uranium tetrafluoride is dehydrated by heating to 350 0 C in an inert gas flow. The complete conversion from UF 4 into UF 6 is achieved by a fluidized-bed reactor and a high value of utilization efficiency of fluorine, over 99.9 percent, is attained at about 400 0 C. (author)

  16. Selection of a management strategy for depleted uranium

    International Nuclear Information System (INIS)

    Patton, S.; Hanrahan, E.; Bradley, C. Jnr.

    1995-01-01

    A consequence of the uranium enrichment process is the accumulation of a significant amount of depleted uranium hexafluoride (UF 6 ). Currently, in the United States approximately 560 000 tonnes of the material are stored at three different sites. The US Department of Energy (DOE) has recently initiated a programme to consider alternative strategies for the cost-effective and environmentally safe long-term management of this inventory of depleted UF 6 . The programme involves a technology and engineering assessment of proposed management options (which are: use/reuse, conversion, storage, or disposal) and an analysis of the potential environmental impacts and life-cycle costs of alternative management strategies. The information obtained from the studies will be used by the DOE to select a preferred long-term management strategy. Because of its provisions for considering a wide range of relevant issues and involving the public, this programme has become a model for future DOE materials disposition programmes. This paper presents an overview of the Depleted Uranium Hexafluoride Management Programme. Technical findings of the programme to date are presented, and major issues involved in selecting and implementing a management strategy are discussed. (author)

  17. Electrodeposition of uranium in stirred liquid cadmium cathode

    International Nuclear Information System (INIS)

    Koyama, T.; Tanaka, H.

    1997-01-01

    The electrodeposition of U in a liquid Cd cathode was known to be hampered by the formation of dendritic U on the Cd surface. Electrotransports of uranium to the stirred liquid Cd cathode were carried out at 773 K for different cathode current densities and different Reynolds number of stirring. The maximum amount of U taken in the liquid Cd cathode without forming dendrites was found to increase with an increasing Reynolds number of stirring and decrease with increasing cathode current density. (orig.)

  18. Transport of uranium by supported liquid membrane containing bis(2-ethylhexyl) hydrogenphosphate and 1-octanol

    International Nuclear Information System (INIS)

    Akiba, Kenichi; Kanno, Takuji; Takahashi, Toshihiko.

    1984-01-01

    Carrier-mediated transport of uranium(VI) has been studied by means of liquid membranes impregnated in a microporous polymer. Liquid membranes containing bis(2-ethylhexyl) hydrogenphosphate (DEHPA) alone yielded inadequate stripping of uranium. The addition of 1-octanol to DEHPA solutions resulted in a decrease in extractability, and made it possible to control the distribution ratio of uranium. Uranium in the feed solution was sufficiently transported across the liquid membrane containing this DEHPA-1-octanol mixture into the product solution. The apparent rate constant (ksub(obs)) of transport increased slightly with an increase in carrier concentrations. Variations in acid concentrations of the feed solution (pH 2.5--3.2) and the product solution (0.1--1.0 M H 2 SO 4 ) had little effect on the transport rate. A large excess of uranium, more than the carrier content in the liquid membrane, was finally concentrated in the stripping acid. (author)

  19. Distribution of uranium supply and enrichment

    International Nuclear Information System (INIS)

    Bamford, F.W.

    1982-01-01

    Uranium supply and demand is examined from the perspective of companies in the uranium hexafluoride (UF6) conversion business whose main interest is their sources of uranium supply and UF6 destinations because of transportation costs. Because of the variations in yellowcake transport, charges for conversion, and UF6 transport costs, most converters don't have standard prices. Companies try to look ahead to determine patterns of supplies and delivery points when they analyze the market and estimate future prices. Market analyses must take into account the purchasing policies of utilities around the world. The presentation shows North America supplying about 40% of world uranium, with about 13% of the enrichment done elsewhere. It also shows North American converters getting 53% of the business, but that will require importing uranium from outside North America. 6 tables

  20. Description of an engineering-scale facility for uranium fluorination studies

    International Nuclear Information System (INIS)

    Yagi, Eiji; Saito, Shinichi; Horiuchi, Masato

    1976-03-01

    In the research program of power reactor fuel reprocessing by fluoride volatility process, the engineering facility was constructed to establish the techniques of handling kilogram quantities of fluorine and uranium hexafluoride and to obtain engineering data on the uranium fluidized-bed oxidation and fluorination. This facility is designed for a capacity of 5 kg per batch. Descriptions on the facility and equipment are given, including design philosophy, safety and its analysis. (auth.)

  1. Contribution to Yttria corrosion study by liquid uranium; Contribution a l`etude de la corrosion de l`yttria par l`uranium liquide

    Energy Technology Data Exchange (ETDEWEB)

    Tournier, C

    1995-02-01

    We are studying liquid uranium and polycrystalline Yttria interactions under secondary vacuum. The type, morphology and thickness of interfacial reaction products between U and Y{sub 2}O{sub 3} are examined by optical and confocal microscopy, SEM, X ray diffraction, X analysis and XPS. The most important parameters are the stoechiometry and microstructure of the Yttria, the oxygen partial pressure of the furnace atmosphere, pO{sub 2}, and the duration and temperature of experiments. In the thermodynamic modelization, we take into account exchanges at the ceramic/metal interface and exchanges between the molten metal and the furnace atmosphere. Liquid uranium reacts with Yttria to form UO{sub 2} at the interface which gradually changes into a solid solution UO{sub 2}-Y{sub 2}O{sub 3}. The total thickness of reaction products results from two opposing reactions: (i) oxidation of uranium by Yttria (low pO{sub 2}) or by the atmosphere (high pO{sub 2}), controlled by migration of oxygen vacancies at Yttria grain boundaries. (ii) deoxidation caused by the formation of volatile uranium monoxide. On the other hand, we observed a transition of the type ``non-wettability {yields} wettability `` which occurs subsequent to an increase of the stoichiometric variation x in Y{sub 2}O{sub 3-x}. (author). 69 refs., 76 figs., 30 tabs.

  2. Surface decontamination in the old storage shed number 99 of the General Plan of IPEN/CNEN-SP, containing production equipment of natural uranium hexafluoride (UF6), aiming at its decommissioning

    International Nuclear Information System (INIS)

    Almeida, Claudio C. de; Cambises, Paulo B.S.; Paiva, Julio E. de; Paiva, Julio E. de; Silva, Teresina M.; Rodrigues, Demerval L.

    2013-01-01

    This paper presents the steps adopted in the operation planned for the decontamination of surfaces in the old storage shed number 99 the general layout of the Energy Research and Nuclear IPEN-CNEN/SP, Brazil, and contained various types of equipment originating from production hexafluoride natural uranium (UF6). This operation involved the planning, training of operators of the facility, analysis of workplaces and radiometric surveys for monitoring of external radiation and surface contamination. The training involved the procedures for decontamination of surfaces, segregation of materials and practical procedures for individual monitoring of contamination outside of the body. Were also established rules for the transport of radioactive materials in the internal and external facility and release of material and sites already decontaminated

  3. Performance of a uranium liquid argon calorimeter

    International Nuclear Information System (INIS)

    Tuts, P.M.

    1987-01-01

    The author presents results on the performance of a uranium and liquid argon colorimeter in the NW test beam at Fermilab. This study describes the calorimeter, and discusses its performance with electrons, pions and muons from 10 GeV to 150 GeV. The performance parameters measure response, linearity, resolution, compensation, and e/π separation

  4. Trace recovery of uranium and rare earth contained in phosphates by liquid-liquid extraction in sulfuric attack liquor

    International Nuclear Information System (INIS)

    Bousquet, F.; Foraison, D.; Leveque, A.; Sabot, J.L.

    1980-06-01

    Uranium and rare earths can be recovered in sedimentary phosphates during the wet processing of the ore by sulfuric acid giving raw phosphoric acid at 30 per cent of P 2 O 5 . Practically all the uranium contained and only part of rare earths are put into solution in this treatment. Separation of these elements in the phosphoric solution is obtained by liquid-liquid extraction with alkylphosphoric acids and especially with their mono and di esters. Partition isotherms are determined and counter-current tests are effected. Uranium and rare earths reextraction from these solvents can be simultaneous or separate with aqueous solutions alkaline or containing HF or by antisynergism. Pros and cons of each reextraction process are discussed. In conclusion HDEHP or OPPA are recommended because of availability, stability and hydrodynamic, OPPA less selective with rare earths allows the recovery with uranium of ceric earths, yttrium and yttric earths [fr

  5. Airborne uranium, its concentration and toxicity in uranium enrichment facilities

    International Nuclear Information System (INIS)

    Thomas, J.; Mauro, J.; Ryniker, J.; Fellman, R.

    1979-02-01

    The release of uranium hexafluoride and its hydrolysis products into the work environment of a plant for enriching uranium by means of gas centrifuges is discussed. The maximum permissible mass and curie concentration of airborne uranium (U) is identified as a function of the enrichment level (i.e., U-235/total U), and chemical and physical form. A discussion of the chemical and radiological toxicity of uranium as a function of enrichment and chemical form is included. The toxicity of products of UF 6 hydrolysis in the atmosphere, namely, UO 2 F 2 and HF, the particle size of toxic particulate material produced from this hydrolysis, and the toxic effects of HF and other potential fluoride compounds are also discussed. Results of an investigation of known effects of humidity and temperature on particle size of UO 2 F 2 produced by the reaction of UF 6 with water vapor in the air are reported. The relationship of the solubility of uranium compounds to their toxic effects was studied. Identification and discussion of the standards potentially applicable to airborne uranium compounds in the working environment are presented. The effectiveness of High Efficiency Particulate (HEPA) filters subjected to the corrosive environment imposed by the presence of hydrogen fluoride is discussed

  6. Main results obtained in France in the development of the gaseous diffusion process for uranium isotope separation

    International Nuclear Information System (INIS)

    Frejacques, C.; Bilous, O.; Dixmier, J.; Massignon, D.; Plurien, P.

    1958-01-01

    The main problems which occur in the study of uranium isotope separation by the gaseous diffusion process, concern the development of the porous barrier, the corrosive nature of uranium hexafluoride and also the chemical engineering problems related to process design and the choice of best plant and stage characteristics. Porous barriers may be obtained by chemical attack of non porous media or by agglomeration of very fine powders. Examples of these two types of barriers are given. A whole set of measurement techniques were developed for barrier structure studies, to provide control and guidance of barrier production methods. Uranium hexafluoride reactivity and corrosive properties are the source of many difficult technological problems. A high degree of plant leak tightness must be achieved. This necessity creates a special problem in compressor bearing design. Barrier lifetime is affected by the corrosive properties of the gas, which may lead to a change of barrier structure with time. Barrier hexafluoride permeability measurements have helped to make a systematic study of this point. Finally an example of a plant flowsheet, showing stage types and arrangements and based on a minimisation of enriched product costs is also given as an illustration of some of the chemical engineering problems present. (author) [fr

  7. Results of the remote sensing feasibility study for the uranium hexafluoride storage cylinder yard program

    International Nuclear Information System (INIS)

    Balick, L.K.; Bowman, D.R.

    1997-02-01

    The US DOE manages the safe storage of approximately 650,000 tons of depleted uranium hexafluoride remaining from the Cold War. This slightly radioactive, but chemically active, material is contained in more than 46,000 steel storage cylinders that are located at Oak Ridge, Tennessee; Paducah, Kentucky; and Portsmouth, Ohio. Some of the cylinders are more than 40 years old, and approximately 17,500 are considered problem cylinders because their physical integrity is questionable. These cylinders require an annual visual inspection. The remainder of the 46,000-plus cylinders must be visually inspected every four years. Currently, the cylinder inspection program is extremely labor intensive. Because these inspections are accomplished visually, they may not be effective in the early detection of leaking cylinders. The inspection program requires approximately 12--14 full-time-equivalent (FTE) employees. At the cost of approximately $125K per FTE, this translates to $1,500K per annum just for cylinder inspection. As part of the technology-development portion of the DOE Cylinder Management Program, the DOE Office of Facility Management requested the Remote Sensing Laboratory (RSL) to evaluate remote sensing techniques that have potential to increase the effectiveness of the inspection program and, at the same time, reduce inspection costs and personnel radiation exposure. During two site visits (March and May 1996) to the K-25 Site at Oak Ridge, TN, RSL personnel tested and characterized seven different operating systems believed to detect leakage, surface contamination, thickness and corrosion of cylinder walls, and general area contamination resulting from breached cylinders. The following techniques were used and their performances are discussed: Laser-induced fluorescent imaging; Long-range alpha detection; Neutron activation analysis; Differential gamma-ray attenuation; Compton scatterometry; Active infrared inspection; and Passive thermal infrared imaging

  8. Selectivity of NF membrane for treatment of liquid waste containing uranium

    International Nuclear Information System (INIS)

    Oliveira, Elizabeth E.M.; Barbosa, Celina C.R.; Afonso, Julio C.

    2013-01-01

    The performance of two nanofiltration membranes were investigated for treatment of liquid waste containing uranium through two conditions permeation: permeation test and concentration test of the waste. In the permeation test solution permeated returned to the feed tank after collected samples each 3 hours. In the test of concentration the permeated was collected continuously until 90% reduction of the feed volume. The liquid waste ('carbonated water') was obtained during conversion of UF 6 to UO 2 in the cycle of nuclear fuel. This waste contains uranium concentration on average 7.0 mg L -1 , and not be eliminated to the environmental. The waste was permeated using a cross-flow membrane cell in the pressure of the 1.5 MPa. The selectivity of the membranes for separation of uranium was between 83% and 90% for both tests. In the concentration tests the waste was concentrated around for 5 times. The surface layer of the membranes was evaluated before and after the tests by infrared spectroscopy (ATR-FTIR), field emission microscopy (FESEM) and atomic force spectroscopy (AFM). The membrane separation process is a technique feasible to and very satisfactory for treatment the liquid waste. (author)

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

    Science.gov (United States)

    Visser, Ann E; Bridges, Nicholas J

    2014-06-10

    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.

  10. Rupture of Model 48Y UF6 cylinder and release of uranium hexafluoride. Cylinder overfill, March 12-13, 1986. Investigation of a failed UF6 shipping container. Volume 2

    International Nuclear Information System (INIS)

    1986-06-01

    NUREG-1179, Volume 1, reported on the rupture of a Model 48Y uranium hexafluoride (UF 6 ) cylinder and the subsequent release of UF 6 . At the time of publication, a detailed metallurgical examination of the damaged cylinder was under way and results were not available. Subsequent to the publication of Volume 1, a second incident occurred at the Sequoyah Fuels Corporation facility. On March 13, 1986, a Model 48X cylinder was overfilled during a special one-time draining procedure; however, no release of UF 6 occurred. An Augmented Investigation Team investigated this second incident. This report, NUREG-1179, Volume 2, presents the findings made by the Augmented Investigation Team of the March 13 incident and the report of the detailed metallurgical examination conducted by Battelle Columbus Division of the cylinder damaged on January 4, 1986

  11. Separation of uranium from aqueous solutions using calix[6]arenes in liquid-liquid extraction as well as solid phase extraction

    International Nuclear Information System (INIS)

    Schmeide, K.; Geipel, G.; Bernhard, G.

    2004-11-01

    The suitability of different calyx[n] arene types for uranyl extraction from liquid solutions was examined by means of liquid-liquid extraction using aqueous phases and organic solvents of varying compositions. It was found that COOH-derivatised calyx[6] arenes have good extraction properties and can even be used in the acid pH range. The use of calixarene-modified fleeces for the separation of uranyl from aqueous phases was examined in batch experiments with pH and uranyl concentration as variables and in the presence or absence of competing ions. The results showed that calixarene-modified fleeces can be used for uranium separation starting from pH 4. At pH 5, up to a maximum of 7.6 x 10 -7 mol uranium can be bound per 1 g of calixarene-modified fleece. The separation of uranyl from synthetic pit waters was examined as a means of testing the separation capacity of calixarene-modified fleeces in environmentally sensitive waters. Studies on the reversibility of uranium bonding to calixarene-treated polyester fleeces have shown that under environmentally realistic conditions (neutral pH range) the uranium is firmly bound to the calixarene-modified fleeces and cannot be mobilised. By contrast, in acidic environments calixarene-modified fleeces are capable of near-complete regeneration. Such regenerated textile filter materials can then be used for further uranium separation cycles [de

  12. Application of the HGSYSTEM/UF6 model to simulate atmospheric dispersion of UF6 releases from uranium enrichment plants

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  13. The preparation of uranium tetrafluoride from dioxide by aqueous way

    International Nuclear Information System (INIS)

    Aquino, A.R. de; Abrao, A.

    1990-01-01

    This paper describes the study for the wet way obtention of uranium tetrafluoride by the reaction of hydrofluoric acid and powder uranium dioxide. With the results obtained at laboratory scale a pilot plant was planned and erected. It is presently in operation for experimental data aquisition. Time of reaction, temperature, excess of reagents and the hydrofluoric acid / uranium dioxide ratio were the main parameters studied to obtain a product with the following characteristics: - density greater than 1 g/cm 3 , - conversion rate greater than 96%, -water content equal to 0,2%, that allows its application to hexafluoride convertion or to magnesiothermic process. (authOr) [pt

  14. Ningyo Toge uranium enrichment pilot plant comes into full

    International Nuclear Information System (INIS)

    1982-01-01

    The uranium enrichment pilot plant of the Power Reactor and Nuclear Fuel Development Corporation at Ningyo Toge went into full operation on March 26, 1982. This signifies that the front end of the nuclear fuel cycle in Japan, from uranium ore to enrichment, is only a step away from commercialization. On the same day, the pilot plant of uranium processing and conversion to UF 6 , the direct purification of uranium ore into uranium hexafluoride, began batch operation at the same works. The construction of the uranium enrichment pilot plant has been advanced in three stages: i.e. OP-1A with 1000 centrifuges, OP-1B with 3000 centrifuges and OP-2 with 3000 centrifuges. With a total of 7000 centrifuges, the pilot plant, the first enrichment plant in Japan, has now a capacity of supplying enriched uranium for six months operation of a 1,000 MW nuclear power plant. (J.P.N.)

  15. The physics of uranium isotope separation by laser

    International Nuclear Information System (INIS)

    Clerc, M.; Rigny, P.

    1985-01-01

    SILMO is the isotopic separation process using a laser and the uranium hexafluoride molecule. SILVA is the laser process whereby the enriched medium is formed by the atomic vapour from uranium. The scientific bases of the two processes are described using very simple parameters such as photoionisation selectivity and useful availability of photons and atoms. It is shown that SILVA can have a specific energy consumption lower than 100 KWh/UTS. A separator module could be made up, for instance, of a dihedron of uranium vapour several metres long in which the laser beams would have to be bent within a multi-duct cell to cover about 180 to 200 meters. This separator module would use overall laser light power of some 10 KW and could supply 3.5% enriched uranium in a single phase from natural uranium by rejecting 0.20% impoverished U. 27 refs [fr

  16. Technology, Safety and Costs of Decommissioning a Reference Uranium Hexafluoride Conversion Plant

    Energy Technology Data Exchange (ETDEWEB)

    Elder, H. K.

    1981-10-01

    Safety and cost information is developed for the conceptual decommissioning of a commercial uranium hexafluoride conversion (UF{sub 6}) plant. Two basic decommissioning alternatives are studied to obtain comparisons between cost and safety impacts: DECON, and passive SAFSTOR. A third alternative, DECON of the plant and equipment with stabilization and long-term care of lagoon wastes. is also examined. DECON includes the immediate removal (following plant shutdown) of all radioactivity in excess of unrestricted release levels, with subsequent release of the site for public use. Passive SAFSTOR requires decontamination, preparation, maintenance, and surveillance for a period of time after shutdown, followed by deferred decontamination and unrestricted release. DECON with stabilization and long-term care of lagoon wastes (process wastes generated at the reference plant and stored onsite during plant operation} is also considered as a decommissioning method, although its acceptability has not yet been determined by the NRC. The decommissioning methods assumed for use in each decommissioning alternative are based on state-of-the-art technology. The elapsed time following plant shutdown required to perform the decommissioning work in each alternative is estimated to be: for DECON, 8 months; for passive SAFSTOR, 3 months to prepare the plant for safe storage and 8 months to accomplish deferred decontamination. Planning and preparation for decommissioning prior to plant shutdown is estimated to require about 6 months for either DECON or passive SAFSTOR. Planning and preparation prior to starting deferred decontamination is estimated to require an additional 6 months. OECON with lagoon waste stabilization is estimated to take 6 months for planning and about 8 months to perform the decommissioning work. Decommissioning cost, in 1981 dollars, is estimated to be $5.91 million for OECON. For passive SAFSTOR, preparing the facility for safe storage is estimated to cost $0

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

    International Nuclear Information System (INIS)

    2003-01-01

    This document is a site-specific environmental impact statement (EIS) for construction and operation of a proposed depleted uranium hexafluoride (DUF 6 ) conversion facility at the U.S. Department of Energy (DOE) Paducah site in northwestern Kentucky (Figure S-1). The proposed facility would convert the DUF 6 stored at Paducah to a more stable chemical form suitable for use or disposal. In a Notice of Intent (NOI) published in the ''Federal Register'' (FR) on September 18, 2001 (''Federal Register'', Volume 66, page 48123 [66 FR 48123]), DOE announced its intention to prepare a single EIS for a proposal to construct, operate, maintain, and decontaminate and decommission two DUF 6 conversion facilities at Portsmouth, Ohio, and Paducah, Kentucky, in accordance with the National Environmental Policy Act of 1969 (NEPA) (''United States Code'', Title 42, Section 4321 et seq. [42 USC 4321 et seq.]) and DOE's NEPA implementing procedures (''Code of Federal Regulations'', Title 10, Part 1021 [10 CFR Part 1021]). Subsequent to award of a contract to Uranium Disposition Services, LLC (hereafter referred to as UDS), Oak Ridge, Tennessee, on August 29, 2002, for design, construction, and operation of DUF 6 conversion facilities at Portsmouth and Paducah, DOE reevaluated its approach to the NEPA process and decided to prepare separate site-specific EISs. This change was announced in a ''Federal Register'' Notice of Change in NEPA Compliance Approach published on April 28, 2003 (68 FR 22368); the Notice is included as Attachment B to Appendix C of this EIS. This EIS addresses the potential environmental impacts from the construction, operation, maintenance, and decontamination and decommissioning (DandD) of the proposed conversion facility at three alternative locations within the Paducah site; from the transportation of depleted uranium conversion products to a disposal facility; and from the transportation, sale, use, or disposal of the fluoride-containing conversion products

  18. Evaluation of transport properties of nanofiltration membranes exposed to radioactive liquid waste

    Energy Technology Data Exchange (ETDEWEB)

    Oliveira, Elizabeth E.M.; Barbosa, Celina C.R.; Bastos, Edna T.R., E-mail: eemo@ien.gov.br [Instituto de Engenharia Nuclear (IEN/CNEN-RJ), Rio de Janeira, RJ (Brazil); Afonso, Julio C., E-mail: Julio@iq.ufrj.br [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Inst. de Quimica. Dept. de Quimica Analitica

    2011-07-01

    The application of membrane separation processes (PSM) for treatment of radioactive waste requires the selection of a suitable membrane for the treatment of waste, as the membrane will be directly exposed to the radioactive liquid waste, and also exposed to ionizing radiation. The nanofiltration membrane is most suitable for treatment of radioactive waste, since it has high rejection of multivalent ions. Usually the membranes are made of polymers and depending on the composition of the waste, type and dose of radiation absorbed may be changes in the structure of the membrane, resulting in loss of its transport properties. We tested two commercial nanofiltration membranes: NF and SW Dow/Filmtec. The waste liquid used was obtained in the process of conversion of uranium hexafluoride gas to solid uranium dioxide, known as 'carbonated water'. The membranes were characterized as their transport properties (hydraulic permeability, permeate flux and salt rejection) before and after their immersion in the waste for 24 hours. The surface of the membranes was also evaluated by SEM and FTIR. It was observed that in both the porosity of the membrane selective layer was altered, but not the membrane surface charge, which is responsible for the selectivity of the membrane. The NF membranes and SW showed uranium ion rejection of 64% and 55% respectively. (author)

  19. Bibliographical study on photochemical separation of uranium isotopes

    International Nuclear Information System (INIS)

    Bougon, Roland

    1975-01-01

    The objective of this report is to propose an overview of knowledge and current works on isotopic separation of uranium by means of selective excitation where this excitation is obtained by a light source with a wave length corresponding to a selective or preferential absorption by a molecule or by the atom itself of one of the isotopes. After a brief overview of principles and requirements of isotopic separation by selective excitation, the author reviews compounds which can be used for this process. These compounds are mainly considered in terms of spectroscopy, and the study focuses on the most volatile among them, the uranium hexafluoride, its spectra, and possible processes for extraction. Some much less volatile uranium compounds are also mentioned with, when available, their spectroscopic properties. The uranium vapour excitation process is described, and some orientations for further researches are proposed [fr

  20. Review of experience gained in fabricating nuclear grade uranium and thorium compounds and their analytical quality control at the Instituto de Energia Atomica, Sao Paulo, Brazil

    International Nuclear Information System (INIS)

    Abrao, A.; Franca Junior, J.M.; Ikuta, A.

    1977-01-01

    The main activities developed at 'Instituto de Energia Atomica' Sao Paulo, Brazil, on the recovery of uranium from ores, the purification of uranium and thorium raw concentrates and their transformation in nuclear grade compounds, are reviewed. The design and assemble of pilot facilities for ammonium diuranate (ADV) uranium tetrafluoride, uranium trioxide, uranium oxide microspheres, uranyl nitrate denitration, uranim hexafluoride and thorium compounds are discussed. The establishment of analytical procedures are emphasized [pt

  1. Fluorine nuclear magnetic resonance study of enrichment effects in gaseous, liquid and solid uranium hexafluoride

    International Nuclear Information System (INIS)

    Ursu, I.; Demco, D.E.; Simplaceanu, V.; Valcu, N.

    1977-01-01

    The nuclear magnetic resonance method is able to provide information concerning the isotopic content of 235 U in UF 6 by means of measuring the nuclear magnetic transverse relaxation time (T,L2) of 19 F nuclei in liquid UF 6 . In this work, the sources of errors in the T 2 measurements have been analysed and methods for reducing them are dicussed. Typical errors in T 2 determinations are below 2%. The enrichment estimations made by using the linear calibration curves had a deviation of less than 2% with some exceptions. It was found that the chemical impurities may significantly affect the enrichment estimations. 19 F NMR spectra of liquid and gaseous UF 6 at low pressures did not reveal any structure or enrichment effect. The longitudinal nuclear magnetic relaxation of 19 F nuclei in low pressure, gaseous and solid UF 6 showed no enrichment dependence, nor the dipolar relaxation time in solid UF 6 did. (author)

  2. Reaction of water vapor with a clean liquid uranium surface

    International Nuclear Information System (INIS)

    Siekhaus, W.

    1985-01-01

    To study the reaction of water vapor with uranium, we have exposed clean liquid uranium surfaces to H 2 O under UHV conditions. We have measured the surface concentration of oxygen as a function of exposure, and determined the maximum attainable surface oxygen concentration X 0 /sup s/ as a function of temperature. We have used these measurements to estimate, close to the melting point, the solubility of oxygen (X 0 /sup b/, -4 ) and its surface segregation coefficient β/sup s/(> 10 3 ). 8 refs., 5 figs., 1 tab

  3. Technology for down-blending weapons grade uranium into commercial reactor-usable uranium

    International Nuclear Information System (INIS)

    Arbital, J.G.; Snider, J.D.

    1996-01-01

    The US Department of Energy (DOE) is evaluating options for rendering surplus inventories of highly enriched uranium (HEU) incapable of being used in nuclear weapons. Weapons-capable HEU was earlier produced by enriching the uranium isotope 235 U from its natural occurring 0.71 percent isotopic concentration to at least 20 percent isotopic concentration. Now, by permanently diluting the concentration of the 235 U isotope, the weapons capability of HEU can be eliminated in a manner that is reversible only through isotope re-enrichment, and therefore, highly resistant to proliferation. To the extent that can be economically and technically justified, the down-blended, low-enriched uranium product will be made suitable for use as commercial reactor fuel. Such down-blended uranium product can also be disposed of as waste if chemical or isotopic impurities preclude its use as reactor fuel. The DOE has evaluated three candidate processes for down blending surplus HEU. These candidate processes are: (1) uranium hexafluoride blending; (2) molten uranium metal blending; and (3) uranyl nitrate solution blending. This paper describes each of these candidate processes. It also compares the relative advantages and disadvantages of each process with respect to: (1) the various forms and compounds of HEU comprising the surplus inventory, (2) the use of down-blended product as commercial reactor fuel, or (3) its disposal as waste

  4. No fluorinated compounds in the uranium conversion process: risk analysis and proposition of pictograms; Os compostos nao fluorados nos processos da conversao do uranio: analise de riscos e proposicao de pictogramas

    Energy Technology Data Exchange (ETDEWEB)

    Jeronimo, Adroaldo Clovis; Oliveira, Wagner dos Santos, E-mail: acejota18@yahoo.com.br, E-mail: oliveira@feq.unicamp.br [Universidade Estadual de Campinas (UNICAMP), SP (Brazil). Fac. de Engenharia Quimica; Aquino, Afonso Rodrigues de, E-mail: araquino@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2012-03-15

    The plants comprising the chemical conversion of uranium, which are part of the nuclear fuel cycle, present some risks, among others, because are associated with the non-fluorinated compounds handled in these processes. This study is the analysis of the risks associated with these compounds, i e, the non-fluorinated reactants and products, handled in different chemical processing plants, which include the production of uranium hexafluoride, while emphasizing the responsibilities and actions that fit to the chemical engineer with regard to minimizing risks during the various stages. The work is based on the experience gained during the development and mastery of the technology of production of uranium hexafluoride, the IPEN/ CNEN-SP, during the '80s, with the support of COPESP -Navy of Brazil. (author)

  5. A rapid method to estimate uranium using ionic liquid as extracting agent from basic aqueous media

    International Nuclear Information System (INIS)

    Prabhath Ravi, K.; Sathyapriya, R.S.; Rao, D.D.; Ghosh, S.K.

    2016-01-01

    Room temperature ionic liquids, as their name suggests are salts with a low melting point typically less than 100 °C and exist as liquid at room temperature. The common cationic parts of ionic liquids are imidazolium, pyridinium, pyrrolidinium, quaternary ammonium, or phosphonium ions, and common anionic parts are chloride, bromide, boron tetrafluorate, phosphorous hexafluorate, triflimide etc. The physical properties of ionic liquids can be tuned by choosing appropriate cations with differing alkyl chain lengths and anions. Application of ionic liquids in organic synthesis, liquid-liquid extractions, electrochemistry, catalysis, speciation studies, nuclear reprocessing is being studied extensively in recent times. In this paper a rapid method to estimate the uranium content in aqueous media by extraction with room temperature ionic liquid tricaprylammoniumthiosalicylate ((A- 336)(TS)) followed by liquid scintillation analysis is described. Re-extraction of uranium from ionic liquid phase to aqueous phase was also studied

  6. Study of neptunium hexafluoride formation and its adsorption on metallic fluorides

    International Nuclear Information System (INIS)

    Matcheret, Georges

    1970-01-01

    This report involves two parts. The first part deals with the action of elementary fluorine on neptunium compounds by a thermogravimetric method. The mechanism and the kinetics of this reaction vary according to the nature of the compound. 1 - With neptunium tetrafluoride the reaction, proceeds in a single step. The kinetics corresponds to a uniform attack of the entire surface of the sample and follows the kinetics law: (1-α) 1/3 1-k rel t . 2 - The reaction with neptunium dioxyde involves two steps, neptunium tetrafluoride being the intermediate compound. The kinetics of the first step corresponds to a diffusion process and follows the kinetic law: log (1-α) = kt 1/2 . The kinetics of the second step corresponds to an uniform attack of the entire sur face of the sample. The object of the second part is a study of the adsorption of uranium hexafluoride and neptunium hexafluoride on sodium, magnesium and barium fluorides by a volumetric method. The adsorption of UF 6 on MgF 2 has been investigated at 20 deg. C. The isothermal curve obtained is characteristic of a physical one layer monomolecular adsorption. In a way similar to the behaviour of UF 6 the adsorption of NpF 6 involves in addition a chemical reduction with formation of NpF 5 and release of fluorine. The reaction of NpF 6 with BaF 2 permitted to confirm the influence of the polarizing power of the Ba ++ ion on formation and stability of the product of addition. (author) [fr

  7. An experimental study of molten salt electrorefining of uranium using solid iron cathode and liquid cadmium cathode for development of pyrometallurgical reprocessing

    International Nuclear Information System (INIS)

    Koyama, Tadafumi; Iizuka, Masatoshi; Tanaka, Hiroshi; Tokiwai, Moriyasu; Shoji, Yuichi; Fujita, Reiko; Kobayashi, Tsuguyuki.

    1997-01-01

    Electrorefining of uranium was studied for developing pyrometallurgical reprocessing technology of metal fuel cycle. After concentration dependence of polarization curve was measured, uranium was electrodeposited either on solid iron cathode or in liquid cadmium cathode. Design and operational conditions of the cathode were improved for obtaining much greater quantity of deposit, resulting in recovery of 732g of dendritic uranium on a single solid cathode, and of 232g of uranium in 2,344g of a liquid cadmium cathode. The behaviors of electro-codeposition of rare earth elements with uranium were observed for liquid cadmium cathode, and were found to follow the local equilibrium between salt electrolyte and cathode. The decontamination factors of FP simulating elements from uranium were tentatively determined as >2,000 for deposition to solid cathode and as >7 for deposition to liquid cadmium cathode, respectively. (author)

  8. South Australia, uranium enrichment

    International Nuclear Information System (INIS)

    1976-02-01

    The Report sets out the salient data relating to the establishment of a uranium processing centre at Redcliff in South Australia. It is conceived as a major development project for the Commonwealth, the South Australian Government and Australian Industry comprising the refining and enrichment of uranium produced from Australian mines. Using the data currently available in respect of markets, demand, technology and possible financial return from overseas sales, the project could be initiated immediately with hexafluoride production, followed rapidly in stages by enrichment production using the centrifuge process. A conceptual development plan is presented, involving a growth pattern that would be closely synchronised with the mining and production of yellowcake. The proposed development is presented in the form of an eight-and-half-year programme. Costs in this Report are based on 1975 values, unless otherwise stated. (Author)

  9. Gasket for uranium enrichment plant

    Energy Technology Data Exchange (ETDEWEB)

    Kishi, S; Aiyoshi, H

    1977-02-08

    A gasket to be inserted between flange joints in the equipments and pipe lines of an uranium enrichment plant having neither permeability nor adsorptivity to water while maintaining mechanical, physical and chemical properties of an elastomer gasket is described. A gasket made of an elastomeric material such as a polymer is integratedly formed at its surface with anti-slip projections. The gasket is further surrounded at its upper and lower peripheral sides, as well as outer circumferential portion with a U-sectioned cover (enclosure) made of fluoro-plastics. In this arrangement, the gasket main body shows a gas-tightness for uranium hexafluoride gas and the cover exhibits a gas-tightness for other component gases such as moisture to thereby prevent degradation of the gasket due to absorption and permeation of the moisture.

  10. Production of uranium dioxide

    International Nuclear Information System (INIS)

    Hart, J.E.; Shuck, D.L.; Lyon, W.L.

    1977-01-01

    A continuous, four stage fluidized bed process for converting uranium hexafluoride (UF 6 ) to ceramic-grade uranium dioxide (UO 2 ) powder suitable for use in the manufacture of fuel pellets for nuclear reactors is disclosed. The process comprises the steps of first reacting UF 6 with steam in a first fluidized bed, preferably at about 550 0 C, to form solid intermediate reaction products UO 2 F 2 , U 3 O 8 and an off-gas including hydrogen fluoride (HF). The solid intermediate reaction products are conveyed to a second fluidized bed reactor at which the mol fraction of HF is controlled at low levels in order to prevent the formation of uranium tetrafluoride (UF 4 ). The first intermediate reaction products are reacted in the second fluidized bed with steam and hydrogen at a temperature of about 630 0 C. The second intermediate reaction product including uranium dioxide (UO 2 ) is conveyed to a third fluidized bed reactor and reacted with additional steam and hydrogen at a temperature of about 650 0 C producing a reaction product consisting essentially of uranium dioxide having an oxygen-uranium ratio of about 2 and a low residual fluoride content. This product is then conveyed to a fourth fluidized bed wherein a mixture of air and preheated nitrogen is introduced in order to further reduce the fluoride content of the UO 2 and increase the oxygen-uranium ratio to about 2.25

  11. F{sup 19} relaxation in non-magnetic hexafluorides; Contribution a l'etude de la relaxation des fluors dans les hexafluorures non magnetiques

    Energy Technology Data Exchange (ETDEWEB)

    Rigny, P [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1967-12-01

    The interesting properties of the fluorine magnetic resonance in the hexafluorides of molybdenum, tungsten and uranium, are very much due to large anisotropies of the chemical shift tensors. In the solid phases these anisotropies, the values of which are deduced from line shape studies, allow one to show that the molecules undergo hindered rotations about the metal atom. The temperature and frequency dependence of the fluorine longitudinal relaxation times shows that the relaxation is due to the molecular motion. The dynamical parameters of this motion are then deduced from the complete study of the fluorine relaxation in the rotating frame. In the liquid phases, the existence of anisotropies allows an estimation of the different contributions to the relaxation. In particular, the frequency and temperature dependence of the relaxation shows it to be dominated by the spin-rotation interaction. We have shown that the strength of this interaction can be deduced from the chemical shifts, and the angle through which the molecule rotates quasi-freely can be determined. In the hexafluorides, this angle is roughly one radian at 70 C, and with the help of this value, the friction coefficients which describe the intermolecular interactions are discussed. (author) [French] Les proprietes de la resonance magnetique des fluors dans les hexafluorures de molybdene, tungstene et uranium sont influencees par l'existence de deplacements chimiques tres anisotropes. Dans les phases solides, la valeur de cette anisotropie peut etre determinee par l'analyse des formes de raies et son existence permet de montrer que les molecules sont en rotation empechee autour de leur atome central. L'etude du temps de relaxation longitudinal en fonction de la temperature et de la frequence montre que la relaxation est due aux mouvements moleculaires, aux plus hautes temperatures. Les proprietes dynamiques du mouvement sont obtenues par l'etude complete de la relaxation spin-reseau dans le referentiel

  12. Radiation protection training at uranium hexafluoride and fuel fabrication plants

    International Nuclear Information System (INIS)

    Brodsky, A.; Soong, A.L.; Bell, J.

    1985-05-01

    This report provides general information and references useful for establishing or operating radiation safety training programs in plants that manufacture nuclear fuels, or process uranium compounds that are used in the manufacture of nuclear fuels. In addition to a brief summary of the principles of effective management of radiation safety training, the report also contains an appendix that provides a comprehensive checklist of scientific, safety, and management topics, from which appropriate topics may be selected in preparing training outlines for various job categories or tasks pertaining to the uranium nuclear fuels industry. The report is designed for use by radiation safety training professionals who have the experience to utilize the report to not only select the appropriate topics, but also to tailor the specific details and depth of coverage of each training session to match both employee and management needs of a particular industrial operation. 26 refs., 3 tabs

  13. Transformations of highly enriched uranium into metal or oxide; Etudes des procedes de transformation des composes d'uranium a fort enrichissement isotopique

    Energy Technology Data Exchange (ETDEWEB)

    Nollet, P; Sarrat, P [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1964-07-01

    The enriched uranium workshops in Cadarache have a double purpose on the one hand to convert uranium hexafluoride into metal or oxide, and on the other hand to recover the uranium contained in scrap materials produced in the different metallurgical transformations. The principles that have been adopted for the design and safety of these workshops are reported. The nuclear safety is based on the geometrical limitations of the processing vessels. To establish the processes and the technology of these workshops, many studies have been made since 1960, some of which have led to original achievements. The uranium hexafluoride of high isotopic enrichment is converted either by injection of the gas into ammonia or by an original process of direct hydrogen reduction to uranium tetrafluoride. The uranium contained m uranium-zirconium metal scrap can be recovered by combustion with hydrogen chloride followed treatment of the uranium chloride by fluorine in order to obtain the uranium in the hexafluoride state. Recovery of the uranium contained m various scrap materials is obtained by a conventional refining process combustion of metallic scrap, nitric acid dissolution of the oxide, solvent purification by tributyl phosphate, ammonium diuranate precipitation, calcining, reduction and hydro fluorination into uranium tetrafluoride, bomb reduction by calcium and slag treatment. Two separate workshops operate along these lines one takes care of the uranium with an isotopic enrichment of up to 3 p. 100, the other handles the high enrichments. The handling of each step of this process, bearing in mind the necessity for nuclear safety, has raised some special technological problems and has led to the conception of new apparatus, in particular the roasting furnace for metal turnings, the nitric acid dissolution unit, the continuous precipitator and ever safe filter and dryer for ammonium diuranate, the reduction and hydro fluorination furnace and the slag recovery apparatus These are

  14. Process for decontamination of surfaces in an facility of natural uranium hexafluoride production (UF{sub 6}); Processo de descontaminação de superfícies em uma instalação de produção de hexafluoreto de urânio natural (UF{sub 6})

    Energy Technology Data Exchange (ETDEWEB)

    Almeida, Claudio C. de; Silva, Teresinha M.; Rodrigues, Demerval L.; Carneiro, Janete C.G.G., E-mail: calmeida@ipen.br [Instituto de Pesquisas Energéticas e Nucleares(IPEN/CNEN-SP), São Paulo, SP (Brazil). Gerência de Radioproteção

    2017-07-01

    The experience acquired in the actions taken during the decontamination process of an IPEN-CNEN / SP Nuclear and Energy Research Institute facility, for the purpose of making the site unrestricted, is reported. The steps of this operation involved: planning, training of facility operators, workplace analysis and radiometric measurements. The facility had several types of equipment from the natural uranium hexafluoride (UF{sub 6}) production tower and other facility materials. Rules for the transportation of radioactive materials were established, both inside and outside the facility and release of materials and installation.

  15. New method for conversion of uranium hexafluoride to uranium dioxide

    International Nuclear Information System (INIS)

    Nakabayashi, S.; Suzuki, M.; Tanaka, H.

    1987-01-01

    Five different methods for conversion of UF 6 to ceramic-grade UO 2 powder have been developed to industrial scale. Two of them, the ammonium diuranate (ADU) and AUC processes, are based on precipitation of uranium compounds from aqueous solutions. The other three follow a dry route in which UF 6 is hydrolyzed and reduced by steam and hydrogen using fluidized bed techniques, rotating kilns, or flame chemistry methods. The ADU process has the advantage of flexible product powder characteristics, while disadvantages include a large quantity of waste, low powder fluidity, and a complicated process. On the other hand, the dry process using fluidized-bed techniques has the advantages of hydrofluoric acid recovery, a free-flowing powder, and process simplicity, but the disadvantages of poorer ceramic properties for the product. The new method developed at Mitsubishi Metal Corp. is a semidry process, which has well-balanced merits over the ADU process and the dry process using fluidized-bed techniques. This process is very attractive from powder characteristics, process simplicity, and waste reduction

  16. The Determination of Uranium and Trace Metal Impurities in Yellow Cake Sample by Chemical Method

    International Nuclear Information System (INIS)

    Busamongkol, Arporn; Rodthongkom, Chouvana

    1999-01-01

    The purity of uranium cake is very critical in nuclear-grade uranium (UO 2 ) and uranium hexafluoride (UF 6 ) production. The major element in yellow cake is uranium and trace metal impurities. The objective of this study is to determine uranium and 25 trace metal impurities; Aluminum, Barium, Bismuth, Calcium, Cadmium, Cobalt, Chromium, Copper, Iron, Potassium, Iithium, Magnesium, Manganese, Molybdenum, Sodium, Niobium, Nickel, Lead, Antimony, Tin, Strontium, Titanium, Vanadium, Zinc and Zirconium, Uranium is determined by Potassium dichromate titration, after solvent extraction with Cupferon in Chloroform, Trace metal impurities are determined by solvent extraction with Tributyl Phosphate in Carbon-tetrachloride ( for first 23 elements) and N-Benzoyl-N-Phenylhydroxylamine in Chloroform ( for last 2 elements), then analyzed by Atomic Absorption Spectrophotometer (AAS) compared with Inductively Couple Plasma Spectrophotometers (ICP). The accuracy and precision are studied with standard uranium octaoxide

  17. LEAK: A source term generator for evaluating release rates from leaking vessels

    International Nuclear Information System (INIS)

    Clinton, J.H.

    1994-01-01

    An interactive computer code for estimating the rate of release of any one of several materials from a leaking tank or broken pipe leading from a tank is presented. It is generally assumed that the material in the tank is liquid. Materials included in the data base are acetonitrile, ammonia, carbon tetrachloride, chlorine, chlorine trifluoride, fluorine, hydrogen fluoride, nitric acid, nitrogen tetroxide, sodium hydroxide, sulfur hexafluoride, sulfuric acid, and uranium hexafluoride. Materials that exist only as liquid and/or vapor over expected ranges of temperature and pressure can easily be added to the data base file. The Fortran source code for LEAK and the data file are included with this report

  18. Recovery of valuable products from the raffinate of uranium and thorium pilot-plant

    International Nuclear Information System (INIS)

    Martins, E.A.J.

    1990-01-01

    IPEN-CNEN/SP has being very active in refining yellow cake to pure ammonium diuranate which is converted to uranium trioxide, uranium dioxide, uranium tetra-and hexa-fluoride in sequential way. The technology of the thorium purification and its conversion to nuclear grade products has been a practice since several years as well. For both elements the major waste to be worked is the raffinate from purification via TBP-varsol in pulsed columns. In this paper the actual processing technology is reviewed with special emphasis on the recovery of valuable products, mainly nitric acid, ammonium nitrate, uranium, thorium and rare earth elements. Ammonium nitrate from the precipitation of uranium diuranate is of good quality, being radioactivity and uranium-free, and recommended to be applied as fertilizer. In conclusion the main effort is to maximize the recycle and reuse of the above mentioned chemicals. (author)

  19. Wetland assessment of the effects of construction and operation of a depleted uranium hexafluoride conversion facility at the Portsmouth, Ohio, site

    International Nuclear Information System (INIS)

    Van Lonkhuyzen, R.

    2005-01-01

    The U.S. Department of Energy (DOE) Depleted Uranium Hexafluoride (DUF 6 ) Management Program evaluated alternatives for managing its inventory of DUF 6 and issued the ''Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted Uranium Hexafluoride'' (DUF 6 PEIS) in April 1999 (DOE 1999). The DUF 6 inventory is stored in cylinders at three DOE sites: Paducah, Kentucky; Portsmouth, Ohio; and East Tennessee Technology Park (ETTP), near Oak Ridge, Tennessee. In the Record of Decision for the DUF 6 PEIS, DOE stated its decision to promptly convert the DUF 6 inventory to a more stable chemical form. Subsequently, the U.S. Congress passed, and the President signed, the ''2002 Supplemental Appropriations Act for Further Recovery from and Response to Terrorist Attacks on the United States'' (Public Law No. 107-206). This law stipulated in part that, within 30 days of enactment, DOE must award a contract for the design, construction, and operation of a DUF 6 conversion plant at the Department's Paducah, Kentucky, and Portsmouth, Ohio, sites, and for the shipment of DUF 6 cylinders stored at ETTP to the Portsmouth site for conversion. This wetland assessment has been prepared by DOE, pursuant to Executive Order 11990 (''Protection of Wetlands'') and DOE regulations for implementing this Executive Order as set forth in Title 10, Part 1022, of the ''Code of Federal Regulations'' (10 CFR Part 1022 [Compliance with Floodplain and Wetland Environmental Review Requirements]), to evaluate potential impacts to wetlands from the construction and operation of a conversion facility at the DOE Portsmouth site. Approximately 0.02 acre (0.009 ha) of a 0.08-acre (0.03-ha) palustrine emergent wetland would likely be eliminated by direct placement of fill material during facility construction at Location A. Portions of this wetland that are not filled may be indirectly affected by an altered hydrologic regime because of the

  20. Biological assessment of the effects of construction and operation of a depleted uranium hexafluoride conversion facility at the Portsmouth, Ohio,site

    International Nuclear Information System (INIS)

    Van Lonkhuyzen, R.

    2005-01-01

    The U.S. Department of Energy (DOE) Depleted Uranium Hexafluoride (DUF 6 ) Management Program evaluated alternatives for managing its inventory of DUF 6 and issued the ''Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted Uranium Hexafluoride'' (DUF 6 PEIS) in April 1999 (DOE 1999). The DUF 6 inventory is stored in cylinders at three DOE sites: Paducah, Kentucky; Portsmouth, Ohio; and East Tennessee Technology Park (ETTP), near Oak Ridge, Tennessee. In the Record of Decision for the DUF 6 PEIS, DOE stated its decision to promptly convert the DUF 6 inventory to a more stable chemical form. Subsequently, the U.S. Congress passed, and the President signed, the ''2002 Supplemental Appropriations Act for Further Recovery from and Response to Terrorist Attacks on the United States'' (Public Law No. 107-206). This law stipulated in part that, within 30 days of enactment, DOE must award a contract for the design, construction, and operation of a DUF 6 conversion plant at the Department's Paducah, Kentucky, and Portsmouth, Ohio, sites, and for the shipment of DUF 6 cylinders stored at ETTP to the Portsmouth site for conversion. This biological assessment (BA) has been prepared by DOE, pursuant to the National Environmental Policy Act of 1969 and the Endangered Species Act of 1974, to evaluate potential impacts to federally listed species from the construction and operation of a conversion facility at the DOE Portsmouth site. The Indiana bat is known to occur in the area of the Portsmouth site and may potentially occur on the site during spring or summer. Evaluations of the Portsmouth site indicated that most of the site was found to have poor summer habitat for the Indiana bat because of the small size, isolation, and insufficient maturity of the few woodlands on the site. Potential summer habitat for the Indiana bat was identified outside the developed area bounded by Perimeter Road, within the corridors

  1. Measurement system analysis (MSA) of the isotopic ratio for uranium isotope enrichment process control

    Energy Technology Data Exchange (ETDEWEB)

    Medeiros, Josue C. de; Barbosa, Rodrigo A.; Carnaval, Joao Paulo R., E-mail: josue@inb.gov.br, E-mail: rodrigobarbosa@inb.gov.br, E-mail: joaocarnaval@inb.gov.br [Industrias Nucleares do Brasil (INB), Rezende, RJ (Brazil)

    2013-07-01

    Currently, one of the stages in nuclear fuel cycle development is the process of uranium isotope enrichment, which will provide the amount of low enriched uranium for the nuclear fuel production to supply 100% Angra 1 and 20% Angra 2 demands. Determination of isotopic ration n({sup 235}U)/n({sup 238}U) in uranium hexafluoride (UF{sub 6} - used as process gas) is essential in order to control of enrichment process of isotopic separation by gaseous centrifugation cascades. The uranium hexafluoride process is performed by gas continuous feeding in separation unit which uses the centrifuge force principle, establishing a density gradient in a gas containing components of different molecular weights. The elemental separation effect occurs in a single ultracentrifuge that results in a partial separation of the feed in two fractions: an enriched on (product) and another depleted (waste) in the desired isotope ({sup 235}UF{sub 6}). Industrias Nucleares do Brasil (INB) has used quadrupole mass spectrometry (QMS) by electron impact (EI) to perform isotopic ratio n({sup 235}U)/n({sup 238}U) analysis in the process. The decision of adjustments and change te input variables are based on the results presented in these analysis. A study of stability, bias and linearity determination has been performed in order to evaluate the applied method, variations and systematic errors in the measurement system. The software used to analyze the techniques above was the Minitab 15. (author)

  2. Thermodynamic properties of UF sub 6 measured with a ballistic piston compressor

    Science.gov (United States)

    Sterritt, D. E.; Lalos, G. T.; Schneider, R. T.

    1973-01-01

    From experiments performed with a ballistic piston compressor, certain thermodynamic properties of uranium hexafluoride were investigated. Difficulties presented by the nonideal processes encountered in ballistic compressors are discussed and a computer code BCCC (Ballistic Compressor Computer Code) is developed to analyze the experimental data. The BCCC unfolds the thermodynamic properties of uranium hexafluoride from the helium-uranium hexafluoride mixture used as the test gas in the ballistic compressor. The thermodynamic properties deduced include the specific heat at constant volume, the ratio of specific heats for UF6, and the viscous coupling constant of helium-uranium hexafluoride mixtures.

  3. Evaluation of nanofiltration membranes for treatment of liquid radioactive waste

    International Nuclear Information System (INIS)

    Oliveira, Elizabeth Eugenio de Mello

    2013-01-01

    The physicochemical behavior of two nanofiltration membranes for treatment of a low-level radioactive liquid waste (carbonated water) was investigated through static, dynamic and concentration tests. This waste was produced during conversion of uranium hexafluoride (UF 6 ) to uranium dioxide (UO 2 ) in the cycle of nuclear fuel. This waste contains about 7.0 mg L -1 of uranium and cannot be discarded to the environment without an adequate treatment. In static tests membrane samples were immersed in the waste for 24 to 5000 h. Their transport properties (hydraulic permeability, permeate flux, sulfate and chloride ions rejection) were evaluated before and after immersion in the waste using a permeation flux front system under 0.5 MPa. The selective layer (polyamide) was characterized by zeta potential, contact angle, scanning electron microscopy for field emission, atomic force microscopy, infrared spectroscopy, x-ray fluorescence and thermogravimetric analysis before and after static tests. In dynamic tests the waste was permeated under 0.5 MPa, and the membranes showed rejection to uranium above 85% were obtained. The short-term static tests (24-72 h) showed that the selective layer and surface charge of the membranes were not chemical changed, according infrared spectra data. After 5000 h a coating layer was released from the membranes, poly(vinyl alcohol), PVA. After this loss the rejection for uranium decreased. Permeation and concentration of the waste were carried out in permeation flux tangential system under 1.5 MPa. The rejection of uranium was around 90% for permeation tests. In concentration tests the permeated was collected continuously until about 80% reduction of the feed volume. The rejection of uranium was of the 97%. The nanofiltration membranes tested were efficient to concentrate the uranium from the waste. (author)

  4. Development of ammonium uranyl carbonate reduction to uranium dioxide using fluidized bed

    International Nuclear Information System (INIS)

    Gomes, R.P.; Riella, H.G.

    1988-01-01

    Laboratory development of Ammonium Uranyl Carbonate (AUC) reduction to uranium dioxide (UO 2 ) using fluidized bed furnace technique is described. The reaction is carried out at 500-550 0 C using hydrogen, liberated from cracking of ammonia, as a reducing agent. As the AUC used is obtained from uranium hexafluoride (UF 6 ) it contains considerable amounts of fluoride ( - 500μgF - /gTCAU) as contaminant. The presence of fluoride leads to high corrosion rates and hence the fluoride concentrations is reduced by pyrohydrolisis of UO 2 . Physical and Chemical proterties of the final product (UO 2 ) obtained were characterized. (author) [pt

  5. Operation of the D0 uranium liquid-argon calorimeter system

    International Nuclear Information System (INIS)

    Guida, J.

    1992-12-01

    The DO calorimeter consists of three separate cryostats containing uranium modules in liquid argon. This odorimeter has transverse segmentation of 0.1 x 0.1 in η x 0 and consists of eight or nine longitudinal readout segments. The coverage in η extends to 4. As a result of the large coverage and fine segmentation there are 50,000 channels of electronics. After a brief description of the electronics, stability and noise aspects will be investigated. Results of the liquid-argon purity studies will be discssed. The backgrounds in the calorimeter due to the Fermilab main ring will also be examined

  6. Seismic design of a uranium conversion plant building

    International Nuclear Information System (INIS)

    Peixoto, O.J.M.; Botelho, C.L.A.; Braganca, A. Jr.; C. Santos, S.H. de.

    1992-01-01

    The design of facilities with small radioactive inventory has been traditionally performed following the usual criteria for industrial buildings. In the last few years, more stringent criteria have been adopted in new nuclear facilities in order to achieve higher standards for environmental protection. In uranium conversion plants, the UF 6 (uranium hexafluoride) production step is the part of the process with the highest potential for radioactivity release to the environment because of the operations performed in the UF 6 desublimers and cylinder filling areas as well as UF 6 distillation facilities, when they are also required in the process. This paper presents the design guidelines and some details of the seismic resistance design of a UF 6 production building to be constructed in Brazil

  7. A study of UF4 preparations

    International Nuclear Information System (INIS)

    Chang, I.S.; Doh, J.B.; Choi, Y.D.

    1985-05-01

    Uranium tetrafluoride (UF 4 ), green salt, is very important intermediate in the production of metallic uranium and uranium hexafluoride (UF 6 ) for enrichment. The hydrofluorination of uranium dioxide (UO 2 ) with anhydrous hydrogen fluoride (HF), produced from ADU (ammonium diuranate) process or AUC (ammonium uranyl carbonate) process, are commercially used for the production of uranium tetrafluoride. At present, a new approach such as direct UF 4 preparation at the mine-site without further precipitation, filteration and drying of yellow cake from leaching solution has been studied. The single step continous reduction of uranium hexafluoride to uranium tetrafluoride is one of the most interesting process being applied for the commercial use of a large amount of depleted UF 6 which is produced in tail after enrichment. The direct conversion of UF 6 and UF 4 with hydrogen and fluorine gases using cold wall reactor has a certain advantage over various wet process such as AUD and AUC processes in which hydrolysis of UF 6 and various kind of chemicals are required, including liquid waste treatment. This report reviews and analyzes the theory and processes being used commercially or under study. (Author)

  8. The present state of laser isotope separation of uranium

    International Nuclear Information System (INIS)

    Tashiro, Hideo; Nemoto, Koshichi.

    1994-01-01

    As the methods of uranium enrichment, gas diffusion method and centrifugal separation method in which power consumption is less and the cost is low have been carried out. On the other hand, as the future technology, the research and development of laser isotope separation technology have been carried out. There are the atomic laser separation process in which the laser beam of visible light is irradiated to atomic state uranium and the molecular laser separation process in which far infrared laser beam is irradiated to uranium hexafluoride molecules. The atomic process is divided into three steps, that is, the processes of uranium evaporation, the reaction of uranium with laser beam and the recovery of enriched uranium. The principle of the laser separation is explained. The state of development of laser equipment and separation equipment is reported. The principle and the present state of development of the molecular separation process which consists of the cooling of UF 6 gas, the generation of high power 16 μm laser pulses and the collection of the reaction product are explained. The present state of both processes in foreign countries is reported. (K.I.)

  9. Radium 226 and uranium isotopes simultaneously determination in water samples using liquid scintillation counter

    International Nuclear Information System (INIS)

    Al-Masri, M.S.; Al-Akel, B.; Saaid, S.; Nashawati, A.

    2007-04-01

    In this work a method has been developed to determine simultaneously Radium 226 and Uranium isotopes in water samples by low back ground Liquid Scintillation Counter. Radium 226 was determined by its progeny Polonium 214 after one month of sample storage in order to achieve the equilibrium between Radium 226 and Polonium 214. Uranium isotopes were determined by subtracting Radium 226 activity from total alpha activity. The method detection limits were 0.049 Bq/L and 0.176 Bq/L for Radium 226 and Uranium isotopes respectively. The repeatability limits were ± 0.32 Bq/L and ± 0.9 Bq/L for Radium 226 and Uranium isotopes respectively. While relative errors were % 9.5 and %18.2 for Radium 226 and Uranium isotopes respectively. On the other hand, the report presented the results of different standard and natural samples.(author)

  10. Kinetics study of the fluorination of uranium tetrafluoride in a fluidized bed reactor

    International Nuclear Information System (INIS)

    Khani, M.H.; Pahlavanzadeh, H.; Ghannadi, M.

    2008-01-01

    The kinetics of reaction of the uranium tetrafluoride conversion to the uranium hexafluoride with fluorine gas taking place in a fluidized bed reactor operating in industrial conditions have been studied. The external and internal diffusion effects are investigated by Mears and Weisz-Prater criterions. The kinetic equation for the fluorination of uranium tetrafluoride is developed in the absence of diffusional limitation using an integral method by assuming that the gas flow is of plug or perfectly mixed type. A good agreement is observed between the experimental data and a first-order model with respect to fluorine in the CSTR system. The activation energy of the reaction and the pre-exponential factor are obtained using analytical results from a better model

  11. Present state and problems of uranium fuel fabrication businesses

    International Nuclear Information System (INIS)

    Yuki, Akio

    1981-01-01

    The businesses of uranium fuel fabrication converting uranium hexafluoride to uranium dioxide powder and forming fuel assemblies are the field of most advanced industrialization among nuclear fuel cycle industries in Japan. At present, five plants of four companies engage in this business, and their yearly sales exceeded 20 billion yen. All companies are planning the augmentation of installation capacity to meet the growth of nuclear power generation. The companies of uranium fuel fabrication make the nuclear fuel of the specifications specified by reactor manufacturers as the subcontractors. In addition to initially loaded fuel, the fuel for replacement is required, therefore the demand of uranium fuel is relatively stable. As for the safety of enriched uranium flowing through the farbicating processes, the prevention of inhaling uranium powder by workers and the precaution against criticality are necessary. Also the safeguard measures are imposed so as not to convert enriched uranium to other purposes than peacefull ones. The strict quality control and many times of inspections are carried out to insure the soundness of nuclear fuel. The growth of the business of uranium fuel fabrication and the regulation of the businesses by laws are described. As the problems for the future, the reduction of fabrication cost, the promotion of research and development and others are pointed out. (Kako, I.)

  12. A neutron multiplicity analysis method for uranium samples with liquid scintillators

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Hao, E-mail: zhouhao_ciae@126.com [China Institute of Atomic Energy, P.O.BOX 275-8, Beijing 102413 (China); Lin, Hongtao [Xi' an Reasearch Institute of High-tech, Xi' an, Shaanxi 710025 (China); Liu, Guorong; Li, Jinghuai; Liang, Qinglei; Zhao, Yonggang [China Institute of Atomic Energy, P.O.BOX 275-8, Beijing 102413 (China)

    2015-10-11

    A new neutron multiplicity analysis method for uranium samples with liquid scintillators is introduced. An active well-type fast neutron multiplicity counter has been built, which consists of four BC501A liquid scintillators, a n/γdiscrimination module MPD-4, a multi-stop time to digital convertor MCS6A, and two Am–Li sources. A mathematical model is built to symbolize the detection processes of fission neutrons. Based on this model, equations in the form of R=F*P*Q*T could be achieved, where F indicates the induced fission rate by interrogation sources, P indicates the transfer matrix determined by multiplication process, Q indicates the transfer matrix determined by detection efficiency, T indicates the transfer matrix determined by signal recording process and crosstalk in the counter. Unknown parameters about the item are determined by the solutions of the equations. A {sup 252}Cf source and some low enriched uranium items have been measured. The feasibility of the method is proven by its application to the data analysis of the experiments.

  13. Main results obtained in France in the development of the gaseous diffusion process for uranium isotope separation; Principaux resultats obtenus en France dans les etudes sur la separation des isotopes de l'uranium par diffusion gazeuse

    Energy Technology Data Exchange (ETDEWEB)

    Frejacques, C; Bilous, O; Dixmier, J; Massignon, D; Plurien, P [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1958-07-01

    The main problems which occur in the study of uranium isotope separation by the gaseous diffusion process, concern the development of the porous barrier, the corrosive nature of uranium hexafluoride and also the chemical engineering problems related to process design and the choice of best plant and stage characteristics. Porous barriers may be obtained by chemical attack of non porous media or by agglomeration of very fine powders. Examples of these two types of barriers are given. A whole set of measurement techniques were developed for barrier structure studies, to provide control and guidance of barrier production methods. Uranium hexafluoride reactivity and corrosive properties are the source of many difficult technological problems. A high degree of plant leak tightness must be achieved. This necessity creates a special problem in compressor bearing design. Barrier lifetime is affected by the corrosive properties of the gas, which may lead to a change of barrier structure with time. Barrier hexafluoride permeability measurements have helped to make a systematic study of this point. Finally an example of a plant flowsheet, showing stage types and arrangements and based on a minimisation of enriched product costs is also given as an illustration of some of the chemical engineering problems present. (author) [French] Les principaux problemes qui se sont poses dans l'etude de la separation des isotopes de l'uranium par diffusion gazeuse, sont ceux relatifs a l'obtention de barrieres poreuses, ceux lies a l'utilisation de l'hexafluorure d'uranium, enfin les problemes de genie chimique relatifs au procede et a l'agencement optimum des etages et des cascades entre elles. On peut obtenir des barrieres poreuses soit par attaque de membranes pleines, soit par agglomeration de poudres de petites dimensions. Des exemples de ces deux types de barrieres seront donnes. L'etude des proprietes de texture des barrieres obtenues, necessaire pour orienter les recherches de

  14. Uranium-scintillator device

    International Nuclear Information System (INIS)

    Smith, S.D.

    1979-01-01

    The calorimeter subgroup of the 1977 ISABELLE Summer Workshop strongly recommended investigation of the uranium-scintillator device because of its several attractive features: (1) increased resolution for hadronic energy, (2) fast time response, (3) high density (i.e., 16 cm of calorimeter per interaction length), and, in comparison with uranium--liquid argon detectors, (4) ease of construction, (5) simple electronics, and (6) lower cost. The AFM group at the CERN ISR became interested in such a calorimeter for substantially the same reasons, and in the fall of 1977 carried out tests on a uranium-scintillator (U-Sc) calorimeter with the same uranium plates used in their 1974 studies of the uranium--liquid argon (U-LA) calorimeter. The chief disadvantage of the scintillator test was that the uranium plates were too small to fully contain the hadronic showers. However, since the scintillator and liquid argon tests were made with the plates, direct comparison of the two types of devices could be made

  15. Study on direct dissolution of U-10Zr alloy and distribution of uranium and zirconium in liquid cadmium

    International Nuclear Information System (INIS)

    Ye Yuxing; Gao Yuan

    1997-09-01

    The effect of dissolution time, temperature, total surface area of U-10Zr alloy pellets and stirring on the dissolution and dissolution rate of uranium in liquid cadmium were studied. Cadmium containing U and Zr dissolved from U-10Zr alloy at 475 degree C and 500 degree C respectively was analyzed with electron microanalyzer. The experimental results show that at 400 degree and 500 degree C with the stirring rate of some 150 r/min, the solubilities of uranium in liquid cadmium are 0.4% and 2.2%, respectively. At the first 30 min, the dissolution rates of U-10Zr alloy pellets are 0.05 g/(cm 2 ·h) and 0.32 g/(cm 2 ·h), respectively. The suitable dissolution conditions for U-10Zr alloy pellets in liquid cadmium (the ratio of the mass of liquid cadmium to that of the pellets ≅7) are: temperature, about 480 degree C; stirring rate, about 150 r/min; dissolution time, 4 h. The distribution of uranium and zirconium in cadmium is homogeneous

  16. The structure of Canada's uranium industry and its future market prospects

    International Nuclear Information System (INIS)

    1981-01-01

    Production of uranium in Canada began in the 1940s to supply the needs of US weapons development. After 1966 a growing demand for uranium for nuclear power production stimulated exploration, and since then the health of the Canadian uranium industry has been tied to the state of the nuclear power industry. Uranium exploration in Canada is carried out mainly by private enterprise, although the federal and two provincial governments compete through crown corporations. Seven companies produce ore, and six have processing plants. Expansion is underway at several existing operations, and some new projects are underway. The industry is strongly dependent on export markets; only about 15 percent of Canadian production is used in the country. There is one uranium refinery which produces UO 2 powder for CANDU reactor fuel and UF 6 for export. The uranium hexafluoride facility is being expanded. Federal government policy affects the uranium industry in the fields of regulation, ownership, safeguards, protection of the domestic industry, and international marketing. The short-term outlook for the industry is deteriorating, with declining uranium prices, but prospects seem considerably brighter in the longer term. Canada has about 12 percent of the world's uranium reserves, and is the second-largest producer. Discovery potential is believed to be excellent

  17. Process and system for isotope separation using the selective vibrational excitation of molecules

    International Nuclear Information System (INIS)

    Woodroffe, J.A.; Keck, J.C.

    1976-01-01

    This invention concerns the separation of isotopes by using the isotopically selective vibrational excitation and the vibration-translation reactions of the excited particles. UF 6 molecular mixed with a carrier gas, such as argon, are directed through a refrigerated chamber lighted by a laser radiation tuned to excite vibrationally the uranium hexafluoride molecules of a particular uranium isotope. The density of the carrier gas is preferably maintained above the density of the uranium hexafluoride to allow a greater collision probability of the vibrationally excited molecules with a carried molecule. In such a case, the vibrationally excited uranium hexafluoride will collide with a carrier gas molecule provoking the conversion of the excitation energy into a translation of the excited molecule, resulting in thermal energy or greater diffusibility than that of the other uranium hexafluoride molecules [fr

  18. Measurement of uranium in soil environment optimization of liquid fluorescent method improvement

    International Nuclear Information System (INIS)

    Qin Guangcheng; Li Yan

    2013-01-01

    Measurement of uranium in soil environment were introduced in this paper optimization improvement fluid fluorescence analysis method. Use 'on the determination of uranium in soil, rocks, etc. Samples of liquid fluorescent method' when measuring low environment soil samples can not meet the required precision of 8% or less in gansu province and method detection limit of 0.3 mg/kg or less. In affecting the method detection limit, recovery rate and precision of the soil sample decomposition temperature, measuring the temperature of the sample, sample pH value measurement, the background fluorescence measurement condition optimization of analysis is determined, the method detection limit of 0.133 mg/kg, the average recovery rate was 96.6%, the precision is 3.80%. The experimental results show that the method can meet the requirements for determination of trace uranium m environment soil samples. (authors)

  19. Department of Energy depleted uranium recycle

    International Nuclear Information System (INIS)

    Kosinski, F.E.; Butturini, W.G.; Kurtz, J.J.

    1994-01-01

    With its strategic supply of depleted uranium, the Department of Energy is studying reuse of the material in nuclear radiation shields, military hardware, and commercial applications. the study is expected to warrant a more detailed uranium recycle plan which would include consideration of a demonstration program and a program implementation decision. Such a program, if implemented, would become the largest nuclear material recycle program in the history of the Department of Energy. The bulk of the current inventory of depleted uranium is stored in 14-ton cylinders in the form of solid uranium hexafluoride (UF 6 ). The radioactive 235 U content has been reduced to a concentration of 0.2% to 0.4%. Present estimates indicate there are about 55,000 UF 6 -filled cylinders in inventory and planned operations will provide another 2,500 cylinders of depleted uranium each year. The United States government, under the auspices of the Department of Energy, considers the depleted uranium a highly-refined strategic resource of significant value. A possible utilization of a large portion of the depleted uranium inventory is as radiation shielding for spent reactor fuels and high-level radioactive waste. To this end, the Department of Energy study to-date has included a preliminary technical review to ascertain DOE chemical forms useful for commercial products. The presentation summarized the information including preliminary cost estimates. The status of commercial uranium processing is discussed. With a shrinking market, the number of chemical conversion and fabrication plants is reduced; however, the commercial capability does exist for chemical conversion of the UF 6 to the metal form and for the fabrication of uranium radiation shields and other uranium products. Department of Energy facilities no longer possess a capability for depleted uranium chemical conversion

  20. Criticality safety concerns of uranium deposits in cascade equipment

    International Nuclear Information System (INIS)

    Plaster, M.J.

    1996-01-01

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

  1. Correlation of radioactive-waste-treatment costs and the environmental impact of waste effluents in the nuclear fuel cycle: conversion of yellow cake to uranium hexafluoride. Part II. The solvent extraction-fluorination process

    Energy Technology Data Exchange (ETDEWEB)

    Sears, M.B.; Etnier, E.L.; Hill, G.S.; Patton, B.D.; Witherspoon, J.P.; Yen, S.N.

    1983-03-01

    A cost/benefit study was made to determine the cost and effectiveness of radioactive waste (radwaste) treatment systems for decreasing the release of radioactive materials and chemicals from a model uranium hexafluoride (UF/sub 6/) production plant using the solvent extraction-fluorination process, and to evaluate the radiological impact (dose commitment) of the release materials on the environment. The model plant processes 10,000 metric tons of uranium per year. Base-case waste treatment is the minimum necessary to operate the process. Effluents meet the radiological requirements listed in the Code of Federal Regulations, Title 10, Part 20 (10 CFR 20), Appendix B, Table II, but may not be acceptable chemically at all sites. Additional radwaste treatment techniques are applied to the base-case plant in a series of case studies to decrease the amounts of radioactive materials released and to reduce the amounts of radioactive materials released and to reduce the radiological dose commitment to the population in the surrounding area. The costs for the added waste treatment operations and the corresponding dose committment are correlated with the annual cost for treatment of the radwastes. The status of the radwaste treatment methods used in the case studies is discussed. Much of the technology used in the advanced cases will require development and demonstration, or else is proprietary and unavailable for immediate use. The methodology and assumptions for the radiological doses are found in ORNL-4992.

  2. Correlation of radioactive-waste-treatment costs and the environmental impact of waste effluents in the nuclear fuel cycle: conversion of yellow cake to uranium hexafluoride. Part II. The solvent extraction-fluorination process

    International Nuclear Information System (INIS)

    Sears, M.B.; Etnier, E.L.; Hill, G.S.; Patton, B.D.; Witherspoon, J.P.; Yen, S.N.

    1983-03-01

    A cost/benefit study was made to determine the cost and effectiveness of radioactive waste (radwaste) treatment systems for decreasing the release of radioactive materials and chemicals from a model uranium hexafluoride (UF 6 ) production plant using the solvent extraction-fluorination process, and to evaluate the radiological impact (dose commitment) of the release materials on the environment. The model plant processes 10,000 metric tons of uranium per year. Base-case waste treatment is the minimum necessary to operate the process. Effluents meet the radiological requirements listed in the Code of Federal Regulations, Title 10, Part 20 (10 CFR 20), Appendix B, Table II, but may not be acceptable chemically at all sites. Additional radwaste treatment techniques are applied to the base-case plant in a series of case studies to decrease the amounts of radioactive materials released and to reduce the amounts of radioactive materials released and to reduce the radiological dose commitment to the population in the surrounding area. The costs for the added waste treatment operations and the corresponding dose committment are correlated with the annual cost for treatment of the radwastes. The status of the radwaste treatment methods used in the case studies is discussed. Much of the technology used in the advanced cases will require development and demonstration, or else is proprietary and unavailable for immediate use. The methodology and assumptions for the radiological doses are found in ORNL-4992

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

    International Nuclear Information System (INIS)

    1995-01-01

    This report describes the Conversion and Blending Facility (CBF) which will have two missions: (1) convert surplus HEU materials to pure HEU UF 6 and a (2) blend the pure HEU UF 6 with diluent UF 6 to produce LWR grade LEU-UF 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

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

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-07-05

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

  5. Measurement of surface temperature profiles on liquid uranium metal during electron beam evaporation

    Energy Technology Data Exchange (ETDEWEB)

    Ohba, Hironori; Shibata, Takemasa [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    1998-11-01

    Surface temperature distributions of liquid uranium in a water-cooled copper crucible during electron beam evaporation were measured. Evaporation surface was imaged by a lens through a band-path filter (650{+-}5 nm) and a double mirror system on a charge coupled device (CCD) camera. The video signals of the recorded image were connected to an image processor and converted to two-dimensional spectral radiance profiles. The surface temperatures were obtained from the spectral radiation intensity ratio of the evaporation surface and a freezing point of uranium and/or a reference light source using Planck`s law of radiation. The maximum temperature exceeded 3000 K and had saturation tendency with increasing electron beam input. The measured surface temperatures agreed with those estimated from deposition rates and data of saturated vapor pressure of uranium. (author)

  6. Depleted uranium: A DOE management guide

    International Nuclear Information System (INIS)

    1995-10-01

    The U.S. Department of Energy (DOE) has a management challenge and financial liability in the form of 50,000 cylinders containing 555,000 metric tons of depleted uranium hexafluoride (UF 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 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 6 to an oxide aggregate that is used in concrete to make dry storage casks

  7. Floodplain/wetland assessment of the effects of construction and operation ofa depleted uranium hexafluoride conversion facility at the Paducah, Kentucky,site.

    Energy Technology Data Exchange (ETDEWEB)

    Van Lonkhuyzen, R.

    2005-09-09

    The U.S. Department of Energy (DOE) Depleted Uranium Hexafluoride (DUF{sub 6}) Management Program evaluated alternatives for managing its inventory of DUF{sub 6} and issued the ''Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted Uranium Hexafluoride'' (DUF{sub 6} PEIS) in April 1999 (DOE 1999). The DUF{sub 6} inventory is stored in cylinders at three DOE sites: Paducah, Kentucky; Portsmouth, Ohio; and East Tennessee Technology Park (ETTP), near Oak Ridge, Tennessee. In the Record of Decision for the DUF{sub 6} PEIS, DOE stated its decision to promptly convert the DUF{sub 6} inventory to a more stable chemical form. Subsequently, the U.S. Congress passed, and the President signed, the ''2002 Supplemental Appropriations Act for Further Recovery from and Response to Terrorist Attacks on the United States'' (Public Law No. 107-206). This law stipulated in part that, within 30 days of enactment, DOE must award a contract for the design, construction, and operation of a DUF{sub 6} conversion plant at the Department's Paducah, Kentucky, and Portsmouth, Ohio, sites, and for the shipment of DUF{sub 6} cylinders stored at ETTP to the Portsmouth site for conversion. This floodplain/wetland assessment has been prepared by DOE, pursuant to Executive Order 11988 (''Floodplain Management''), Executive Order 11990 (Protection of Wetlands), and DOE regulations for implementing these Executive Orders as set forth in Title 10, Part 1022, of the ''Code of Federal Regulations'' (10 CFR Part 1022 [''Compliance with Floodplain and Wetland Environmental Review Requirements'']), to evaluate potential impacts to floodplains and wetlands from the construction and operation of a conversion facility at the DOE Paducah site. Reconstruction of the bridge crossing Bayou Creek would occur within the Bayou Creek 100-year

  8. Fundamental study on decontamination of wastes contaminated by uranium fluorides by using ionic liquids - dissolution and electrochemistry of uranium in 1-butyl-3-methylimidazolium chloride

    International Nuclear Information System (INIS)

    Noriko Asanuma; Yusuke Ohhashi; Yukio Wada; Masayuki Harada; Yasuhisa Ikeda

    2008-01-01

    Treatment method for wastes contaminated uranium fluorides by using ionic liquids as media of pyrochemical process instead of alkali metal chloride molten salts was proposed. In this method, uranium fluorides such as UF 4 or NaF adsorbing UF 6 are dissolved in 1-butyl-3-methylimidazolium chloride (BMICl) and dissolved uranium species are recovered as deposits by electrochemical reduction. Under the atmospheric condition, UF 4 was completely dissolved in BMICl at 100 deg. C. UV-vis absorption spectra of the sample solution indicated that main species of uranium are U(VI) and a part of uranium exists as U(IV). Chemical form of uranium in the NaF adsorbents is Na 3 UO 2 F 5 . Therefore, it was immediately dissolved to BMICl. However, complete dissolution was not achieved. Cyclic voltammetry of the solutions prepared by dissolution experiments was performed. Redox properties of uranium species in each sample were irreversible. It was assigned to reduction of U(VI) to U(IV). As a result of preliminary bulk electrolysis, it was expected that reduction products are deposited on the carbon cathode. (authors)

  9. Method for converting uranium oxides to uranium metal

    Science.gov (United States)

    Duerksen, Walter K.

    1988-01-01

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

  10. Development of a reduction process of ammonium uranyl carbonate to uranium dioxide in a fluidized bed

    International Nuclear Information System (INIS)

    Gomes, R.P.; Riella, H.G.

    1990-07-01

    Laboratory development of ammonium uranyl carbonate (AUC) reduction to uranium dioxide (UO 2 ) using fluidized bed furnace technique is described. The reaction is carried out at 500-550 0 C using hydrogen, liberated from cracking of ammonia, as a reducing agent. As the AUC used is obtained from uranium hexafluoride (UF 6 ) it contains considerable amount of fluoride (approx. 500μg/g) as contaminant. The presence of fluoride leads to high corrosion rates and hence the fluoride concentration is reduced by pyrohydrolisis of UO 2 . Physical and Chemical properties of the final product (UO 2 ) obtained were characterized. (author) [pt

  11. Emergency exposure levels for natural uranium

    International Nuclear Information System (INIS)

    Spoor, N.L.; Harrison, N.T.

    1980-12-01

    An attempt is made to identify the inhalation hazards associated with the over-exposure of workers and of the general public, following an accidental release of uranium hexafluoride. Maximum emergency concentrations are recommended for periods of 10, 30, and 60 minutes. The quantitative aspect of the assessment is considered in the context of the development of exposure standards for chemical substances and this facilitates the derivation of levels which are compatible with occupational and public health experience and attainable by management, and to which most workers and members of the general public may be exposed without adverse effect. The radiological implications are also considered. (author)

  12. Development of a process to reduce the uranium concentration of liquid radioactive waste

    International Nuclear Information System (INIS)

    Fuentealba Toro, Edgardo David

    2015-01-01

    The purpose of radioactive waste management is to prevent the discharge of waste into the biosphere, a function carried out in Chile by the Chilean Nuclear Energy Commission (CCHEN), which stores around 500 [L] of these organic and inorganic waste in cans coming from research of Universities and CCHEN' laboratories. Within the inorganic liquid waste are concentrations of Uranyl salts with sulfates, chlorides and phosphates. The purpose of this work is to develop at laboratory level a process to concentrate and precipitate uranium salts (Sulfate and Uranyl Chloride) present in radioactive liquid effluents, because in the case of these very long period wastes in liquid state, the most widely used processes are aimed at concentrating or extracting radioactive compounds through separation processes, for their conditioning and final storage under conditions whose radiological risk is minimized. The selected process is liquid-liquid extraction, being evaluated solvents such as benzene and kerosene with the following extractants: tri-n-octylphosphine oxide (TOPO), di-2-ethylhexyl phosphoric acid (DEHPA) and Cyanex© 923. To determine the extraction conditions, which allow to reduce the concentration of uranium to values lower than 10 ppm, the extractant concentration was modified from 0.05 to 0.41 [M] with solvent volume / residue (VO/VA) ratios of 0.2 to 0.5, at an initial concentration of 8,446 [gU/L] and subsequent precipitation of uranium extracted by a reaction with ammonium carbonate. From these experimental tests the maximum extraction conditions were determined. To the generated effluents, a second stage of extraction was necessary in order to reduce its concentration below 10 [mg / L]. The experimental tests allowed to reduce the concentration under 2.5 [mgU/L], equivalent to 99.97% extraction efficiency. The tests with Cyanex© 923 in replacement of the TOPO, allowed to obtain similar results and even better in some cases, due to the fact that final

  13. In-SEM Raman microspectroscopy coupled with EDX - a case study of uranium reference particles

    International Nuclear Information System (INIS)

    Stefaniak, Elzbieta A.; Pointurier, Fabien; Marie, Olivier; Truyens, Jan; Aregbe, Yetunde

    2014-01-01

    Information about the molecular composition of airborne uranium-bearing particles may be useful as an additional tool for nuclear safeguards. In order to combine the detection of micrometer-sized particles with the analysis of their molecular forms, we used a hybrid system enabling Raman microanalysis in high vacuum inside a SEM chamber (SEM-SCA system). The first step involved an automatic scan of a sample to detect and save coordinates of uranium particles, along with X-ray microanalysis. In the second phase, the detected particles were relocated in a white light image and subjected to Raman microanalysis. The consecutive measurements by the two beams showed exceptional fragility of uranium particles, leading to their ultimate damage and change of uranium oxidation state. We used uranium reference particles prepared by hydrolysis of uranium hexafluoride to test the reliability of the Raman measurements inside the high vacuum. The results achieved by the hybrid system were verified by using a standalone Raman micro spectrometer. When deposited on exceptionally smooth substrates, uranyl fluoride particles smaller than 1000 nm could successfully be analyzed with the SEM-SCA system. (authors)

  14. Study of uranium matrix interference on ten analytes using inductively coupled plasma atomic emission spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Ghazi, A.A.; Qamar, S.; Atta, M.A. (A.Q. Khan Research Labs., Rawalpindi (Pakistan))

    1993-08-01

    Maximum allowable concentrations of 12 elements in uranium hexafluoride feed for enrichment to reactor grade material (about 3%), vary from 1 to 100 ppm ([mu]g/g). Using an inductively coupled plasma atomic emission spectrometer, 51 lines of tine of these elements (B, Cr, Mo, P, Sb, Si, Ta, Ti, V and W) has been studied with a uranium matrix to investigate the matrix interference on the basis of signal to background (SBR), and background to background ratios (BBR). Detection limits and limits of quantitative determination (LQDs) were calculated for these elements in a uranium matrix using SBR and relative standard deviation of the background signal (RSD[sub B]) approach. In almost all cases, the uranium matrix interference reduces the SBRs to the extent that direct trace analysis is impossible. A uranium sample having known concentrations of impurities (around LQDs) was directly analysed with results that showed reasonable accuracy and precision. (Author).

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

    Energy Technology Data Exchange (ETDEWEB)

    Brim, Cornelia P.

    2013-04-01

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

  16. Nuclear material control and accounting system evaluation in uranium conversion operations

    International Nuclear Information System (INIS)

    Moreira, Jose Pontes

    1994-01-01

    The Nuclear Material Control and Accounting Systems in uranium conversion operations are described. The conversion plant, uses ammonium diuranate (ADU), as starting material for the production of uranium hexafluoride. A combination of accountability and verification measurement is used to verify physical inventory quantities. Two types of inspection are used to minimize the measurements uncertainty of the Material Unaccounted For (MUF) : Attribute inspection and Variation inspection. The mass balance equation is the base of an evaluation of a Material Balance Area (MBA). Statistical inference is employed to facilitate rapid inventory taking and enhance material control of Safeguards. The calculation of one sampling plan for a MBA and the methodology of inspection evaluation are also described. We have two kinds of errors : no detection and false delation. (author)

  17. Application of insoluble tannin to recovery of uranium, TRU and heavy metals elements form radioactive liquid waste

    International Nuclear Information System (INIS)

    Hamaguchi, Kazuhiko; Shirato, Wataru; Nakamura, Yasuo; Matsumura, Tatsuro; Takeshita, Kenji; Nakano, Yoshio

    1999-01-01

    Mitsubishi Nuclear Fuel Co., Ltd. (MNF) has developed a new adsorbent, TANNIX (tread mark), for the recovery of uranium, TRU and heavy metal elements in the liquid waste, in which TANNIX derived from a natural tannin polymer. TANNIX has same advantages that handling is easier than that of standard IX-resin, and that the volume of secondary waste is reduced by burning the used TANNIX. We have replaced its radioactive liquid waste treatment system from the conventional co-precipitation process to adsorption process by using TANNIX. TANNIX was founded to be more effective for the recovery of Pu, TRU, and hexavalent chromium Cr-(VI) as well as Uranium. (author)

  18. Fundamental study on decontamination of wastes contaminated by uranium fluorides by using ionic liquids - dissolution and electrochemistry of uranium in 1-butyl-3-methylimidazolium chloride

    Energy Technology Data Exchange (ETDEWEB)

    Noriko Asanuma [Department of Energy Science and Engineering, School of Engineering, Tokai University 1117 Kitakaname, Hiratsuka-shi, Kanagawa 259-1292 (Japan); Yusuke Ohhashi; Yukio Wada [Ningyo-toge Environmental Engineering Center, Japan Atomic Energy Agency Kagamino-cho, Tomata-gun, Okayama 708-0698 (Japan); Masayuki Harada; Yasuhisa Ikeda [Research Laboratory for Nuclear Reactors, Tokyo Institute of Technology 2-12-1-N1-34 Ookayama, Meguro-ku, Tokyo 152-8550 (Japan)

    2008-07-01

    Treatment method for wastes contaminated uranium fluorides by using ionic liquids as media of pyrochemical process instead of alkali metal chloride molten salts was proposed. In this method, uranium fluorides such as UF{sub 4} or NaF adsorbing UF{sub 6} are dissolved in 1-butyl-3-methylimidazolium chloride (BMICl) and dissolved uranium species are recovered as deposits by electrochemical reduction. Under the atmospheric condition, UF{sub 4} was completely dissolved in BMICl at 100 deg. C. UV-vis absorption spectra of the sample solution indicated that main species of uranium are U(VI) and a part of uranium exists as U(IV). Chemical form of uranium in the NaF adsorbents is Na{sub 3}UO{sub 2}F{sub 5}. Therefore, it was immediately dissolved to BMICl. However, complete dissolution was not achieved. Cyclic voltammetry of the solutions prepared by dissolution experiments was performed. Redox properties of uranium species in each sample were irreversible. It was assigned to reduction of U(VI) to U(IV). As a result of preliminary bulk electrolysis, it was expected that reduction products are deposited on the carbon cathode. (authors)

  19. Biosorption of uranium in radioactive liquid organic waste by coconut fiber

    International Nuclear Information System (INIS)

    Marumo, Julio Takehiro; Ferreira, Eduardo Gurzoni Alvares; Vieira, Ludmila Cabreira; Ferreira, Rafael Vicente de Padua; Silva, Edson Antonio da

    2013-01-01

    Radioactive liquid organic waste needs special attention because the available treatment processes are often expensive and difficult to be managed. Biosorption is a potential technique since it allies low cost with relatively high efficiency. Biosorption has been defined as the property of certain biomolecules to bind and remove selected ions or other molecules from aqueous solutions. Biosorption using vegetable biomass from agricultural waste has become a very attractive technique because it involves the removal of heavy metal ions by low cost biosorbent. This technique could be employed in the treatment of radioactive liquid wastes. Among the biosorbent reported in the literature, coconut fiber (Cocos nucifera L.) is highlighted due to the large number of functional groups in its composition. The aim of this study was to assess the potential of coconut fiber to remove uranium from radioactive liquid organic waste. This work was divided into three stages: 1) Preparation and activation of the coconut fiber; 2) Physical characterization of the biomass, 3) Batch biosorption experiments. Two forms of coconut fiber were tested, raw and activated. The activation was performed with dilute HNO3 and NaOH solutions. The parameters evaluated for physical characterization of biomass were morphological characteristics of coconut fiber, real and apparent density and surface area. The biomass was suspended in 10 ml of solutions prepared with distillate water and radioactive liquid waste for 2 hours in the proportion of 0.2% w/v. After the contact time, the coconut fiber was removed by filtration and the supernatant, analyzed by inductively coupled plasma optical emission spectrometry (ICP-OES).The results were evaluated using Langmuir and Freundlich isotherms. The maximum capacity for the raw coconut fiber was lower than the activated one, removing only 1.14mg/g against 2.61mg/g. These results suggest that biosorption with coconut fiber in activated form can be applied in the

  20. Biosorption of uranium in radioactive liquid organic waste by coconut fiber

    Energy Technology Data Exchange (ETDEWEB)

    Marumo, Julio Takehiro; Ferreira, Eduardo Gurzoni Alvares; Vieira, Ludmila Cabreira; Ferreira, Rafael Vicente de Padua, E-mail: jtmarumo@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Silva, Edson Antonio da, E-mail: edson.silva2@unioeste.br [Universidade Estadual do Oeste do Parana (UNIOESTE), Toledo, PR (Brazil)

    2013-07-01

    Radioactive liquid organic waste needs special attention because the available treatment processes are often expensive and difficult to be managed. Biosorption is a potential technique since it allies low cost with relatively high efficiency. Biosorption has been defined as the property of certain biomolecules to bind and remove selected ions or other molecules from aqueous solutions. Biosorption using vegetable biomass from agricultural waste has become a very attractive technique because it involves the removal of heavy metal ions by low cost biosorbent. This technique could be employed in the treatment of radioactive liquid wastes. Among the biosorbent reported in the literature, coconut fiber (Cocos nucifera L.) is highlighted due to the large number of functional groups in its composition. The aim of this study was to assess the potential of coconut fiber to remove uranium from radioactive liquid organic waste. This work was divided into three stages: 1) Preparation and activation of the coconut fiber; 2) Physical characterization of the biomass, 3) Batch biosorption experiments. Two forms of coconut fiber were tested, raw and activated. The activation was performed with dilute HNO3 and NaOH solutions. The parameters evaluated for physical characterization of biomass were morphological characteristics of coconut fiber, real and apparent density and surface area. The biomass was suspended in 10 ml of solutions prepared with distillate water and radioactive liquid waste for 2 hours in the proportion of 0.2% w/v. After the contact time, the coconut fiber was removed by filtration and the supernatant, analyzed by inductively coupled plasma optical emission spectrometry (ICP-OES).The results were evaluated using Langmuir and Freundlich isotherms. The maximum capacity for the raw coconut fiber was lower than the activated one, removing only 1.14mg/g against 2.61mg/g. These results suggest that biosorption with coconut fiber in activated form can be applied in the

  1. 49 CFR 173.417 - Authorized fissile materials packages.

    Science.gov (United States)

    2010-10-01

    ... for export and import shipments. (2) A residual “heel” of enriched solid uranium hexafluoride may be... made in accordance with Table 2, as follows: Table 2—Allowable Content of Uranium Hexafluoride (UF6... Liters Cubic feet Maximum Uranium 235-enrichment (weight)percent Maximum “Heel” weight per cylinder UF6...

  2. Preliminary study for treatment methodology establishment of liquid waste containing uranium in refining facility lagoon

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Byung Jik; Lee, Kune Woo; Won, Hui Jun; Ahn, Byung Gil; Shim, Joon Bo

    1999-12-01

    The preliminary study which establishes the treatment methodology of the sludge waste containing uranium in the conversion facility lagoon was performed. The property of lagoon liquid waste such as the initial water content, the density including radiochemical analysis results were obtained using the samples taken from the lagoon. The objective of this study is to provide some basically needed materials for selection of the most proper lagoon waste treatment methodology by reviewing the effective processes and methods for minimizing the secondary waste resulting from the treatment and disposition of large amount of radioactive liquid waste according to the facility closing. The lagoon waste can be classified into two sorts, such as supernatant and precipitate. The supernatants contain uranium less than 5 ppm and their water content are about 35 percent. Therefore, supernatants are solutions composed of mainly salt components. However, the precipitates have lots of uranium compound contained in the coagulation matrix, and are formed as two kinds of crystalline structures. The most proper method minimizing the secondary waste would be direct drying and solidification of the supernatants and precipitates after separation of them by filtering. (author)

  3. Recovery of valuable products in the raffinate of the uranium and thorium pilot-plant

    International Nuclear Information System (INIS)

    Jardim, E.A.; Abrao, A.

    1988-11-01

    IPEN-CNEN/SP has being very active in refining yellowcake to pure ammonium diuranate which is converted to uranium trioxide, uranium dioxide, tetra - and hexafluoride in a sequential way. The technology of the thorium purification and its conversion to nuclear grade products has been a practice since several years as well. For both elements the major to be worked is the raffinate from the solvent extraction colum where and thorium are purified via TBP-varsol in pulsed columns. In this paper the actual processing technology is reviewed with special emphasis on the recovery of valuable products, mainly nitric acid and ammonium nitrate. Distilled nitric acid and the final sulfuric acid as residue are recycle. Ammonium nitrate from the precipitation of uranium diuranate is of good quality, being radioactivity and uranium - free, and recommended to be applied as fertilizer. In conclusion the main effort is to maximize the recycle and reuse of the above mentioned chemicals. (author) [pt

  4. Separation of uranium isotopes by gas centrifugation

    International Nuclear Information System (INIS)

    Jordan, I.

    1980-05-01

    The uranium isotope enrichment is studied by means of the countercurrent gas centrifuge driven by thermal convection. A description is given of (a) the transfer and purification of the uranium hexafluoride used as process gas in the present investigation; (b) the countercurrent centrifuge ZG3; (c) the system designed for the introduction and extraction of the process gas from the centrifuge; (d) the measurement of the process gas flow rate through the centrifuge; (e) the determination of the uranium isotopic abundance by mass spectrometry; (f) the operation and mechanical behavior of the centrifuge and (g) the isotope separation experiments, performed, respectively, at total reflux and with production of enriched material. The results from the separation experiments at total reflux are discussed in terms of the enrichment factor variation with the magnitude and flow profile of the countercurrent given by the temperature difference between the rotor covers. As far as the separation experiments with production are concerned, the discussion of their results is presented through the variation of the enrichment factor as a function of the flow rate, the observed asymmetry of the process and the calculated separative power of the centrifuge. (Author) [pt

  5. The Separation Of The Uranium On The Liquid Radioactive Wastes By Using Zeolites

    International Nuclear Information System (INIS)

    Budiyono, ME; Peornomo, Herry; S, Djoko

    2000-01-01

    The experimental investigation on the separation of uranium of liquid radioactive wastes by using zeolite has been carried out. The aims of this investigation was to separate uranium and to determine the solid content of the liquid radioactive waste. This investigation was carried out because zeolite could be used as a good sorption material. The investigation parameters were the number of zeolites, the pH of wastes and the grain size of zeolites. The number of zeolites was varied from 10-100 g, the waste pH was varied from 1-12 and the grain size of zeolites was varied from 20/40-100/200 mesh, each parameters to included in the waste. The conclusion that could be drawn from this investigation were that the best result of the 80 g zeolites used, pH was 9, and the grain size of zeolites was 60/80 mesh, the solid content was 119,46 g/l and efficiency of separation was 81,74 %. As a rule, the solid content in the evaporator process should be about 200-300 g/l

  6. Development and technical implementation of the separation nozzle process for enrichment of uranium 235

    International Nuclear Information System (INIS)

    Syllus Martins Pinto, C.; Voelcker, H.; Becker, E.W.

    1977-12-01

    The separation nozzle process for the enrichment of uranium-235 has been developed at the Karlsruhe Nuclear Research Center as an alternative to the gaseous diffusion and centrifuge process. The separation of uranium isotopes is achieved by the deflection of a jet of uranium hexafluoride mixed with hydrogen. Since 1970, the German company of STEAG, has been involved in the technological development and commercial implementation of the nozzle process. In 1975, the Brazilian company of NUCLEBRAS, and the German company of Interatom, joined the effort. The primary objective of the common activity is the construction of a separation nozzle demonstration plant with an annual capacity of about 200 000 SWU and the development of components of a commercial plant. The paper covers the most important steps in the development and the technical implementation of the process. (orig.) [de

  7. Helium and Sulfur Hexafluoride in Musical Instruments

    Science.gov (United States)

    Forinash, Kyle; Dixon, Cory L.

    2014-01-01

    The effects of inhaled helium on the human voice were investigated in a recent article in "The Physics Teacher." As mentioned in that article, demonstrations of the effect are a popular classroom activity. If the number of YouTube videos is any indication, the effects of sulfur hexafluoride on the human voice are equally popular.…

  8. Qualification for Safeguards Purposes of UF6 Sampling using Alumina – Results of the Evaluation Campaign of ABACC-Cristallini Method

    OpenAIRE

    ESTAEBAN ADOLFO; GAUTIER EDUARDO; MACHADO DA SILVA LUIS; FERNANDEZ MORENO SONIA; RENHA JR GERALDO; DIAS FABIO; PEREIRA DE OLIVEIRA JUNIOR OLIVIO; AMMARAGGI DAVID; MASON PETER; SORIANO MICHAEL; CROATTO PAUL; ZULEGER EVELYN; GIAQUINTO JOSEPH; HEXEL COLE; VERCOUTER THOMAS

    2017-01-01

    The procedure currently used to sample material from process lines in uranium enrichment plants consists of collecting the uranium hexafluoride (UF6) in gaseous phase by desublimation inside a metal sampling cylinder cooled with liquid nitrogen or in certain facilities in a fluorothene P-10 tube type. The ABACC-Cristallini method (A-C method) has been proposed to collect the UF6 (gas) by adsorption in alumina (Al2O3) in the form of uranyl fluoride (UO2F2) (solid). This method uses a fluor...

  9. Correlation of radioactive waste treatment costs and the environmental impact of waste effluents in the nuclear fuel cycle: conversion of yellow cake to uranium hexafluoride. Part I. The fluorination-fractionation process

    Energy Technology Data Exchange (ETDEWEB)

    Sears, M.B.; Blanco, R.E.; Finney, B.C.; Hill, G.S.; Moore, R.E.; Witherspoon, J.P.

    1977-07-01

    A cost/benefit study was made to determine the cost and effectiveness of radioactive waste (radwaste) treatment systems for decreasing the release of radioactive materials and chemicals from a model uranium hexafluoride (UF/sub 6/) production plant using the fluorination-fractionation (dry hydrofluor) process, and to evaluate the radiological impact (dose commitment) of the released materials on the environment. This study is designed to assist in defining the term as low as is reasonably achievable (ALARA) in relation to limiting the release of radioactive materials from nuclear facilities. The model plant processes 10,000 metric tons of uranium per year. Base-case waste treatment is the minimum necessary to operate the process. Effluents meet the radiological requirements listed in the Code of Federal Regulations, Title 10, Part 20 (10 CFR 20), Appendix B, Table II, but may not be acceptable chemically at all sites. Additional radwaste treatment techniques are applied to the base-case plant in a series of case studies to decrease the amounts of radioactive materials released and to reduce the radiological dose commitment to the population in the surrounding area. The costs for the added waste treatment operations and the corresponding dose commitment are calculated for each case. In the final analysis, radiological dose is plotted vs the annual cost for treatment of the radwastes. The status of the radwaste treatment methods used in the case studies is discussed. Much of the technology used in the advanced cases will require development and demonstration or else is proprietary and unavailable for immediate use. The methodology and assumptions for the radiological doses are found in ORNL-4992.

  10. Correlation of radioactive waste treatment costs and the environmental impact of waste effluents in the nuclear fuel cycle: conversion of yellow cake to uranium hexafluoride. Part I. The fluorination-fractionation process

    International Nuclear Information System (INIS)

    Sears, M.B.; Blanco, R.E.; Finney, B.C.; Hill, G.S.; Moore, R.E.; Witherspoon, J.P.

    1977-07-01

    A cost/benefit study was made to determine the cost and effectiveness of radioactive waste (radwaste) treatment systems for decreasing the release of radioactive materials and chemicals from a model uranium hexafluoride (UF 6 ) production plant using the fluorination-fractionation (dry hydrofluor) process, and to evaluate the radiological impact (dose commitment) of the released materials on the environment. This study is designed to assist in defining the term as low as is reasonably achievable (ALARA) in relation to limiting the release of radioactive materials from nuclear facilities. The model plant processes 10,000 metric tons of uranium per year. Base-case waste treatment is the minimum necessary to operate the process. Effluents meet the radiological requirements listed in the Code of Federal Regulations, Title 10, Part 20 (10 CFR 20), Appendix B, Table II, but may not be acceptable chemically at all sites. Additional radwaste treatment techniques are applied to the base-case plant in a series of case studies to decrease the amounts of radioactive materials released and to reduce the radiological dose commitment to the population in the surrounding area. The costs for the added waste treatment operations and the corresponding dose commitment are calculated for each case. In the final analysis, radiological dose is plotted vs the annual cost for treatment of the radwastes. The status of the radwaste treatment methods used in the case studies is discussed. Much of the technology used in the advanced cases will require development and demonstration or else is proprietary and unavailable for immediate use. The methodology and assumptions for the radiological doses are found in ORNL-4992

  11. Study on treatment of radioactive liquid waste from uranium ore processing by the use of nano oxide ferromagnetic

    International Nuclear Information System (INIS)

    Vuong Huu Anh; Nguyen Van Chinh; Nguyen Ba Tien; Doan Thi Thu Hien; Luu Cao Nguyen

    2015-01-01

    Nano oxide ferromagnetic Fe_3O_4 KT which was produced by the Military Institute of Science and Technology were used to adsorbed heavy metal elements in liquid waste. In this report, the nano oxide ferromagnetic Fe_3O_4 KT with the particle size of 80-100 nm and the specific surface area of 50-70 m"2/g was applied to study the adsorption of radioactive elements in the liquid waste of uranium ores processing. The effective parameters on adsorption process included temperature, stirring rate, stirring time, the pH value of the solution, the initial concentration of uranium in solution were investigated. The results showed that the maximum adsorption capacity for uranium of the nano Fe_3O_4 KT was 53.5 mgU/g with conditions such as: room temperature, stirring speed 120 rounds/minute, the pH value of solution was 8, stirring time about 2 hours . From the results obtained, nano Fe_3O_4 KT was tested to treatment real liquid waste of uranium ore processing after removing almost heavy metals and a part of radioactive elements by preliminary precipitation at pH 8. The results were analyzed on the ICP-MS and α, β total activity equipment, the solution concentration after treatment suitable for Vietnamese Technical Regulation on industrial wastewater QCVN 40: 2011 (concentrations of heavy metals; total activity of α and β). (author)

  12. Uranium material removing and recovering device

    International Nuclear Information System (INIS)

    Takita, Shin-ichi.

    1997-01-01

    A uranium material removing and recovering device for use in removing surplus uranium heavy metal (UO 2 ) generated in a uranium handling facility comprises a uranium material removing device and a uranium material recovering device. The uranium material removing device comprises an adsorbing portion filled with a uranium adsorbent, a control portion for controlling the uranium adsorbent of the uranium adsorbing portion by a controlling agent, a uranium adsorbing device connected thereto and a jetting device for jetting the adsorbing liquid to equipments deposited with uranium. The recovering device comprises a recovering apparatus for recovering uranium materials deposited with the adsorbent liquid removed by the jetting device and a recovering tank for storing the recovered uranium materials. The device of the present invention can remove surplus uranium simply and safely, mitigate body's load upon removing and recovering operations, facilitate the processing for the exchange of the adsorbent and reduces the radioactive wastes. (T.M.)

  13. Lessons learned from recent safety related incidents at A Canadian uranium conversion facility

    International Nuclear Information System (INIS)

    Jaferi, Jafir

    2013-01-01

    This paper presents the Canadian Nuclear Safety Commission's (CNSC) regulatory requirements for nuclear fuel facility licensees to report any situation or incident that results or is likely to result in a hazard to the health or safety of any person or the environment and to submit its incident investigation report with cause(s) of the incident and corrective actions taken or planned. In addition, the paper presents two recent safety-related incidents that occurred at a uranium conversion facility in Canada along with their consequences, causes, corrective actions and any lessons learned. The first incident resulted in a release of uranium hexafluoride (UF6) inside the UF6 cylinder filling station and the second one resulted in a spill of uranium tetrafluoride (UF 4 ) slurry inside the UF6 plant. Both incidents had no impact on the workers or the environment. (authors)

  14. Mathematical Modeling for the Extraction of Uranium and Molybdenum with Emulsion Liquid Membrane, Including Industrial Application and Cost Evaluation of the Uranium Recovery

    International Nuclear Information System (INIS)

    Kris Tri Basuki

    2008-01-01

    Emulsion liquid membrane systems are double emulsion drops. Two immiscible phases are separated by a third phase which is immiscible with the other two phases. The liquid membrane systems were classified into two types: (1) carrier mediated mass transfer, (2) mass transfer without any reaction involved. Uranium extraction, molybdenum extraction and solvent extraction were used as purposed elements for each type of the membrane systems in the derivation of their mathematical models. Mass transfer in emulsion liquid membrane (ELM) systems has been modeled by several differential and algebraic equations. The models take into account the following : mass transfer of the solute from the bulk external phase to the external phase-membrane interface; an equilibrium reaction between the solute and the carrier to form the solute-carrier complex at the interface; mass transfer by diffusion of the solute-carrier complex in the membrane phase to the membrane-internal phase interface; another equilibrium reaction of the solute-carrier complex to release the solute at the membrane-internal phase interface into the internal phase. Models with or without the consideration of film resistances were developed and compared. The models developed in this study can predict the extraction rate through emulsion liquid membranes theoretically. All parameters required in the models can be determined before an experimental extraction run. Experimental data from literature (uranium extraction) and (molybdenum extraction and solvent extraction) were used to test the models. The agreements between the theoretical predictions and the experimental data were very good. The advantages of emulsion liquid membrane systems over traditional methods were discussed. The models developed in this research can be used directly for the design of emulsion liquid membrane systems. The results of this study represent a very significant step toward the practical applications of the emulsion liquid membrane

  15. Depleted uranium storage and disposal trade study: Summary report

    Energy Technology Data Exchange (ETDEWEB)

    Hightower, J.R.; Trabalka, J.R.

    2000-02-01

    The objectives of this study were to: identify the most desirable forms for conversion of depleted uranium hexafluoride (DUF6) for extended storage, identify the most desirable forms for conversion of DUF6 for disposal, evaluate the comparative costs for extended storage or disposal of the various forms, review benefits of the proposed plasma conversion process, estimate simplified life-cycle costs (LCCs) for five scenarios that entail either disposal or beneficial reuse, and determine whether an overall optimal form for conversion of DUF6 can be selected given current uncertainty about the endpoints (specific disposal site/technology or reuse options).

  16. Depleted uranium storage and disposal trade study: Summary report

    International Nuclear Information System (INIS)

    Hightower, J.R.; Trabalka, J.R.

    2000-01-01

    The objectives of this study were to: identify the most desirable forms for conversion of depleted uranium hexafluoride (DUF6) for extended storage, identify the most desirable forms for conversion of DUF6 for disposal, evaluate the comparative costs for extended storage or disposal of the various forms, review benefits of the proposed plasma conversion process, estimate simplified life-cycle costs (LCCs) for five scenarios that entail either disposal or beneficial reuse, and determine whether an overall optimal form for conversion of DUF6 can be selected given current uncertainty about the endpoints (specific disposal site/technology or reuse options)

  17. UF{sub 6} cylinder lifting equipment enhancements

    Energy Technology Data Exchange (ETDEWEB)

    Hortel, J.M. [Martin Marietta Energy Systems, Inc., Piketon, OH (United States)

    1991-12-31

    This paper presents numerous enhancements that have been made to the Portsmouth lifting equipment to ensure the safe handling of cylinders containing liquid uranium hexafluoride (UF{sub 6}). The basic approach has been to provide redundancy to all components of the lift path so that any one component failure would not cause the load to drop or cause any undesirable movement.

  18. Fluorinated compounds in the uranium conversion process: risk analysis and proposition of pictograms

    International Nuclear Information System (INIS)

    Jeronimo, Adroaldo Clovis; Oliveira, Wagner dos Santos

    2012-01-01

    In the process of uranium hexafluoride production there are risks that must be taken into account since the time of completing the project chemist, in its conceptual stage, until to the stage of detailed design and are associated with the handling of chemicals, especially fluoride hydrogen and fluorine. This paper aims to address issues related to the prevention of risks related to industrial safety and health and the environment, considering the different stages of the uranium conversion. Take into account the safety warnings of the plant and, accordingly, make the proposition of pictograms adequate to alert operators of care to be taken during the proposition of pictograms adequate to alert operators of care to be taken during the conduct of these chemical processes. (author)

  19. URANIUM BISMUTHIDE DISPERSION IN MOLTEN METAL

    Science.gov (United States)

    Teitel, R.J.

    1959-10-27

    The formation of intermetallic bismuth compounds of thorium or uranium dispersed in a liquid media containing bismuth and lead is described. A bismuthide of uranium dispersed in a liquid metal medium is formed by dissolving uranium in composition of lead and bismuth containing less than 80% lead and lowering the temperature of the composition to a temperature below the point at which the solubility of uranium is exceeded and above the melting point of the composition.

  20. Study contribution to the new international philosophy of the radiological safety system on chemical processing of the natural uranium

    International Nuclear Information System (INIS)

    Silva, T.M. da.

    1988-01-01

    The objective of the work is to adapt the radiological Safety System in the facilities concerned to the chemical treatment of the uranium concentrated (yellow-cake) until conversion in uranium hexafluoride in the pilot plant of IPEN-CNEN/SP, to the new international philosophy adopted by the International Commission Radiological on Protection ICPR publication 22(1973), 26(1977), 30(1978) and the International Atomic Energy Agency IAEA publication 9(1982). The new philosophy changes fully the Radiological Protection concepts of preceding philosophy, changes, also, the concept of the work place and individual monitoring as well as the classification of the working areas. These new concepts are applied in each phase of the natural uranium treatment chemical process in conversion facility. (author)

  1. Hadron and electron response of uranium/liquid argon calorimeter modules for the D0 detector

    International Nuclear Information System (INIS)

    Abolins, M.; Astur, R.; Edmunds, D.; Linnemann, J.T.; Mooney, P.; Owen, D.P.; Pi, B.; Pope, B.G.; Weerts, H.; Ahn, S.C.; Demarteau, M.; Forden, G.E.; Good, M.L.; Grannis, P.D.; Guida, J.A.; Heuring, T.; Marx, M.; McCarthy, R.; Ng, K.K.; Paterno, M.; Schamberger, R.D.; Timko, M.; Aronson, S.H.; Featherly, J.; Gibbard, B.G.; Gordon, H.A.; Guida, J.M.; Guryn, W.; Kahn, S.; Protopopescu, S.; Yamin, P.; Bartlett, J.F.; Bross, A.D.; Christenson, J.H.; Cooper, W.E.; Fisk, H.E.; Haggerty, H.; Ito, A.S.; Johnson, M.E.; Jonckheere, A.M.; Merritt, K.W.; Raja, R.; Smith, R.P.; Treadwell, E.; Blazey, G.C.; Borders, J.; Draper, P.; Durston, S.; Ferbel, T.; Hirosky, R.; Kewley, D.; Libonate, S.; Lobkowicz, F.; Franzini, P.; Tuts, P.M.; Gerecht, J.; Kononenko, W.; Selove, W.; Wang, H.; Hadley, N.J.; Hagopian, S.; Linn, S.; Piekarz, H.; Wahl, H.D.; Yousseff, S.; Klopfenstein, C.; Madaras, R.J.; Spadafora, A.L.; Stevenson, M.L.; Wenzel, W.A.; Kotcher, J.; Kourlas, J.; Nemethy, P.; Nesic, D.; Sculli, J.; Martin, H.J.; Zieminski, A.; Roberts, K.; Wimpenny, S.J.; White, A.P.; Womersley, W.J.

    1989-01-01

    We present the results of tests on two types of uranium/liquid calorimeter modules, one electromagnetic and one hadronic, constructed for the DO detector at the Fermilab Tevatron Collider. For electrons and hardons with energies between 10 and 150 GeV, we present measurements of energy resolution, linearity of response, electromagnetic to hadronic response ratio (e/π), and longitudinal hadronic shower development. We have also investigated the effects of adding small amounts of methane to the liquid argon. (orig.)

  2. Isotope separation using vibrationally excited molecules

    International Nuclear Information System (INIS)

    Woodroffe, J.A.; Keck, J.C.

    1979-01-01

    Vibrational excitation of molecules having components of a selected isotope type is used to produce a conversion from vibrational to translational excitation of the molecules by collision with the molecules of a heavy carrier gas. The resulting difference in translaton between the molecules of the selected isotope type and all other molecules of the same compound permits their separate collection. When applied to uranium enrichment, a subsonic cryogenic flow of molecules of uranium hexafluoride in combination with an argon carrier gas is directed through a cooled chamber that is illuminated by laser radiaton tuned to vibrationally excite the uranium hexafluoride molecules of a specific uranium isotope. The excited molecules collide with carrier gas molecules, causing a conversion of the excitation energy into a translation of the excited molecule, which results in a higher thermal energy or diffusivity than that of the other uranium hexafluoride molecules. The flowing molecules including the excited molecules directly enter a set of cryogenically cooled channels. The higher thermal velocity of the excited molecules increases the probability of their striking a collector surface. The molecules which strike this surface immediately condense. After a predetermined thickness of molecules is collected on the surface, the flow of uranium hexafluoride is interrupted and the chamber heated to the point of vaporization of the collected hexafluoride, permitting its removal. (LL)

  3. Monte Carlo studies of uranium calorimetry

    International Nuclear Information System (INIS)

    Brau, J.; Hargis, H.J.; Gabriel, T.A.; Bishop, B.L.

    1985-01-01

    Detailed Monte Carlo calculations of uranium calorimetry are presented which reveal a significant difference in the responses of liquid argon and plastic scintillator in uranium calorimeters. Due to saturation effects, neutrons from the uranium are found to contribute only weakly to the liquid argon signal. Electromagnetic sampling inefficiencies are significant and contribute substantially to compensation in both systems. 17 references

  4. The regulation of uranium refineries and conversion facilities in Canada

    International Nuclear Information System (INIS)

    Didyk, J.P.

    1986-04-01

    The nuclear regulatory process as it applies to uranium refineries and conversion facilities in Canada is reviewed. In the early 1980s, Eldorado Resources Limited proposed to construct and operate new facilities for refining yellowcake and for the production of uranium hexafluoride (UF 6 ). These projects were subject to regulation by the Atomic Energy Control Board (AECB). A description of the AECB's comprehensive licensing process covering all stages of siting, construction, operation and eventual decommissioning of nuclear facilities is traced as it was applied to the Eldorado projects. The AECB's concern with occupational health and safety, with public health and safety and with the protection of the environment in so far as it affects public health and safety is emphasized. Some regulatory difficulties encountered during the project's development which led to opening up the licensing process to public input and closer coordination of regulatory activities with other provincial and federal regulatory agencies are described. The Board's regulatory operational compliance program for uranium refineries and conversion facilities is summarized

  5. Combination of solid phase extraction and dispersive liquid-liquid microextraction for separation/preconcentration of ultra trace amounts of uranium prior to its fiber optic-linear array spectrophotometry determination.

    Science.gov (United States)

    Dadfarnia, Shayessteh; Shabani, Ali Mohammad Haji; Shakerian, Farid; Shiralian Esfahani, Golnaz

    2013-12-15

    A simple and sensitive method for the separation and preconcentration of the ultra trace amounts of uranium and its determination by spectrophotometry was developed. The method is based on the combination of solid phase extraction and dispersive liquid-liquid microextraction. Thus, by passing the sample through the basic alumina column, the uranyl ion and some cations are separated from the sample matrix. The retained uranyl ion along with the cations are eluted with 5 mL of nitric acid (2 mol L(-1)) and after neutralization of the eluent, the extracted uranyl ion is converted to its anionic benzoate complex and is separated from other cations by extraction of its ion pair with malachite green into small volume of chloroform using dispersive liquid-liquid microextraction. The amount of uranium is then determined by the absorption measurement of the extracted ion pair at 621 nm using flow injection spectrophotometry. Under the optimum conditions, with 500 mL of the sample, a preconcentration factor of 1980, a detection limit of 40 ng L(-1), and a relative standard deviation of 4.1% (n=6) at 400 ng L(-1) were obtained. The method was successfully applied to the determination of uranium in mineral water, river water, well water, spring water and sea water samples. Copyright © 2013 Elsevier B.V. All rights reserved.

  6. Status and prospects of safety research of fuel cycle facilities in France

    International Nuclear Information System (INIS)

    Auchere, H.; Mercier, J.P.

    1996-01-01

    The following themes of research are discussed: prolonged loss of cooling in concentrated fission product solution storage tanks; dewatering of a spent fuel storage pond; explosion risks in nuclear fuel cycle laboratories and plants; dissemination of radioactive materials in case of fire in fuel manufacturing plants and in spent fuel analysis laboratories; contamination transfer; phenomenology of liquid uranium hexafluoride vaporization into the atmosphere; ways and means of intervention in the event of liquid ClF 3 leakage; offsite explosion; seismic research. (K.A.)

  7. Mortality of workers in a factory of uranium conversion in France: situation of the follow up from 1968 to 2005

    International Nuclear Information System (INIS)

    Guseva Canu, I.; Metz, C.; Tirmarche, M.; Caer, S.; Auriol, B.

    2008-01-01

    A cohort of workers of Areva NC of Pierrelatte was constituted to study the effects of the internal irradiation after the incorporation of uranium. Between 1960 and 1996, this establishment provided the uranium hexafluoride enrichment and since 1982, the chemical conversion of the different compounds of yellow cake. The cohort descriptive and the results of mortality are reported. The cohort presents a a good follow up (zero lost sight people) of workers potentially exposed to uranium. Its mortality is similar to this one of other workers (at Areva NC). The effect of the sane worker is important, due essentially to the selection of workers at hiring. The employments-exposures matrix at Pierrelatte will allow to study the effects of exposure on the mortality by cancer. (N.C.)

  8. Electrotransport of Uranium from a Liquid Cadmium Anode to a Solid Cathode

    International Nuclear Information System (INIS)

    Ahluwalia, Rajesh K.; Hua, Thanh Q.

    2002-01-01

    During anodic dissolution of irradiated binary Experimental Breeder Reactor-II fuel, a portion of the electrorefined uranium collects in the underlying cadmium pool. It is periodically recovered by setting up a cell configuration in which the pool is made the anode and uranium is electrodeposited on a solid cathode mandrel. A theoretical model is used to determine the current structure of the liquid cadmium anode. The model is validated by comparing against the measured composition of the cathode deposits. Multinodal simulations are conducted to explain the bell shape of deposits observed with this mode of electrotransport. The simulations also determine the dependence of collection efficiency on the electrical charge passed that is functionally consistent with the experimental data. Finally, a simplified operating map of the electrorefiner is presented that can be used to determine the conditions for growing cathode deposits of target composition

  9. Reaction between molybdenum hexafluoride and carboxylic acids

    International Nuclear Information System (INIS)

    Shustov, L.D.; Nikolenko, L.N.; Senchenkova, T.M.

    1983-01-01

    Trifluoromethyl derivatives of pyridine, imidazole and difluoromethane are synthesized during interaction of MoF 6 surplUs (190-210 deg) with nicotine-isomicotine-, 2,6-pyridinedicarboxylic-, 4,5-imidazoledicarboxyclic- and diffluoroacetic acids. The yield of trifluoromethyl derivatives attains 84%. Molybdenum hexafluoride offers some advantages in comparisoo with toxic SF 4 . MoF 6 toxicity is low; leakage of MoF 6 vapors is easily detected

  10. Laboratory studies on leaching of low grade uranium ores and treatment of low level liquid waste generated by leaching experiments

    International Nuclear Information System (INIS)

    Palabrica, O.T.; Antonino, E.J.; Caluag, L.A.; Villamater, D.

    1980-07-01

    Acid leaching experiments of preconcentrated uranium ore were carried out at a pulp density of 50% solids, using sulfuric acid with sodium chlorate as oxidant. The different leaching parameters considered in this work were temperature, oxidant level and leaching time. In the experimental procedure, the concentration of oxidant and the temperature were varied to determine how they affect the leaching process. Experimental results are illustrated in tabulated form for better interpretation. Uranium analyses were done by fluorimetric and delayed-neutron activation analysis. An anion exchange method using Dowex 1 x 8, 200-400 mesh (Cl - ) was used in treating the low-level liquid waste generated by leaching experiments. The purpose of this treatment was to minimize radioactive contamination in the waste materials and also to recover some of the uranium left in the liquid waste. (author)

  11. Liquid-liquid extraction of uranium from nitric acid solution using di-n-butylsulfoxide in petroleum ether as extractant

    Energy Technology Data Exchange (ETDEWEB)

    Khan, M.H.; Shahida, S. [Dept. of Chemistry, Univ. of Azad Jammu and Kashmir, Muzaffarabad (Pakistan); Ali, A. [Nuclear Chemistry Div., Pakistan Inst. of Nuclear Science and Technology, Nilore, Islamabad (Pakistan)

    2008-07-01

    A simple, efficient and economical liquid-liquid extraction method has been developed for quantitative extraction of uranium from 2 M HNO{sub 3} using di-n-butyl sulfoxide in petroleum ether. The dependence of the partition reaction of U(VI) on the concentration of HNO{sub 3}, extractant and temperature was studied. The reaction was found to be inversely dependent upon the temperature and the values for related thermodynamics functions ({delta}H, {delta}S, {delta}G) for extraction equilibrium were determined to be -33.6 kJ/mol, -1.29 kJ/mol/degree and -0.11 kJ/mol/degree, respectively. The effect of Al(NO{sub 3}){sub 3} as salting-out agent and diverse ions on the extraction was examined. The salting-out agent slightly enhanced the extraction. All cations studied have showed negligible effect on the extraction, whereas phosphate and fluoride interfered seriously. Among others, oxalate, citrate and sulphide ions affect the extraction to a lesser extent. Uranium was successfully extracted from a synthetic mixture of Ti{sup +4}, Zr{sup +4}, Hf{sup +4} and Th{sup +4} using EDTA as masking agent. Among strippants, deionized water was found most suitable, and the recovery of uranium was noted to be {>=} 96%. The stoichiometric composition of the extracted species was found to be UO{sub 2}(NO{sub 3}){sub 2} . 2DBSO. The extraction mechanism is discussed on the basis of the results obtained. The extractant has high loading as well as recycling capacity without any degradation. The method was also applied to the Standard Reference Material (NBL-49) and the measured value was found to be in agreement with the reported value within {+-}2% deviation. (orig.)

  12. The development of the uranium and nuclear industry in South Africa, 1945 - 1970 : a historical study

    International Nuclear Information System (INIS)

    Janson, E.J.G.

    1995-12-01

    This thesis traces the historical development of nuclear research in South Africa between 1945 and 1970, starting with the efforts of metallurgists of South Africa and the Allied Nations to extract uranium from the gold ores of the Witwatersrand. During the 1950's seventeen uranium extraction plants formed a very important part of the country's industrial activity. The prospect of using South African uranium for nuclear power production (in the Western Cape area), led to the Atomic Energy Research and Development Programme investigation into nuclear energy production in South Africa. The programme provided for the refining of uranium for nuclear fuel, the establishment of a nuclear research centre at Pelindaba, the acquisition of a research reactor, and facilities for nuclear reactor research and uranium enrichment experiments. The two major projects that were initiated in the 1960's were the Pelinduna nuclear reactor project and experimentation on the vortex tube method for uranium enrichment (the Gas Cooling Project). An Investigation Committee was appointed by the Government to assess the viability of a pilot uranium enrichment plant. In 1970 it was announced that a process had been developed that was a combination of the separating element using uranium hexafluoride in hydrogen as the process fluid and a new cascade technique. 331 refs., 19 figs

  13. Anodic behavior of uranium in AlCl3-1-ethyl-3-methyl-imidazolium chloride ionic liquid

    Science.gov (United States)

    Jiang, Yidong; Luo, Lizhu; Wang, Shaofei; Bin, Ren; Zhang, Guikai; Wang, Xiaolin

    2018-01-01

    The oxidation state of metals unambiguously affects its anodic behavior in ionic liquid. We systematically investigated the anodic behavior of uranium with different surface oxidation states by electrochemical measurements, spectroscopic methods and surface analysis techniques. In the anodic process, metal uranium can be oxidized to U3+. The corresponding products accumulated on the metal/ILs interface will form a viscous layer. The anodic behavior of uranium is also strongly dependent upon the surface oxide states including thickness and homogeneity of the oxide film. With an increase in the thickness of oxide film, it will be breached at potentials in excess of a critical value. A uniform oxide on uranium surface can be breached evenly, and then the underlying metal starts to dissolve forming a viscous layer which can facilitate uniformly stripping of oxide, thus giving an oxide-free surface. Otherwise, a nonuniform oxide can result in a severe pitted surface with residue oxygen.

  14. Environmental monitoring program design for uranium refining and conversion operations

    International Nuclear Information System (INIS)

    1984-08-01

    The objective of this study was to develop recommendations for the design of environmental monitoring programs at Canadian uranium refining and conversion operations. In order to develop monitoring priorities, chemical and radioactive releases to the air and water were developed for reference uranium refining and conversion facilities. The relative significance of the radioactive releases was evaluated through a pathways analysis which estimated dose to individual members of the critical receptor group. The effects of chemical releases to the environment were assessed by comparing predicted air and water contaminant levels to appropriate standards or guidelines. For the reference facilities studied, the analysis suggested that environmental effects are likely to be dominated by airborne release of both radioactive and nonradioactive contaminants. Uranium was found to be the most important radioactive species released to the air and can serve as an overall indicator of radiological impacts for any of the plants considered. The most important nonradioactive air emission was found to be fluoride (as hydrogen fluoride) from the uranium hexafluoride plant. For the uranium trioxide and uranium dioxide plants, air emissions of oxides of nitrogen were considered to be most important. The study recommendations for the design of an environmental monitoring program are based on consideration of those factors most likely to affect local air and water quality, and human radiation exposure. Site- and facility-specific factors will affect monitoring program design and the selection of components such as sampling media, locations and frequency, and analytical methods

  15. Treatment of liquid effluents from uranium analytical method 'DAVIES & GRAY' by electrodialysis and electrodialysis reactive tests

    International Nuclear Information System (INIS)

    Zuniga Alvear, Karina Andrea

    2014-01-01

    This work describes the process which produces liquid waste coming from the chemical analysis laboratory of the Chilean Nuclear Energy Commission (CCHEN), from the analytical technique called 'Davies and Gray' and their further treatment, using electro dialysis (ED) and reactive electro dialysis (RED), in order to achieve lower uranium contents in solution. The contamination in water is a big problem, since there are many places in the world where is limited. For these reasons new treatments must be done, and the ion-selective membrane has opened a new path for these processes. The radioactive liquid waste have lots of other restrictions in their final disposal, which difficult even more the water recovery, because the law has very strict security margins with respect to these ones. In the case of liquid waste containing uranium, the concern increases, because being the uranium a radioactive element has it has to be lowered at its maximum, or eliminated directly, in order to avoid any kind of contamination. There exist national regulations and international recommendations. They have stipulated the correct management and disposal for radioactive waste. These can come from any uranium production process. In any of these, the liquid waste contains certain uranium content, which after the end of the process; the discarded waste must go through a conditioning and cleaning process for its afterward liberation or recycling. In this study, it was tested the electro dialysis as a radioactive waste treatment, only uranium containing waste coming from the chemical analysis laboratory in CCHEN. The electro dialysis process has a direct competition with other separation process, such as distillation, ionic exchange, and reverse osmosis, among others. The classic electro dialysis has been developed during the 50's, and until today, there has been different version, as inverse, reactive, reversible. The unidirectional and reactive electro dialysis will be the

  16. Experimental study for the use of sulfur hexafluoride as dielectric gas in particle accelerators

    International Nuclear Information System (INIS)

    Candanedo y Bernabe, C.

    1993-01-01

    The sulfur hexafluoride is the better dielectric gas in the world. It is used in particle accelerator, power stations and high voltage transformators. This is a high stable gas, but when is used as dielectric is degraded in toxic and corrosive fluorides this degradation of sulfur hexafluoride is a function of the voltaic arc, crown effect, pressure, temperature and radiation. The purification of the sulfur fluoride permitted to work in safe form and without the risks as contaminant. The objective of the work is the development of a process for the separation of the wastes from the fabrication of sulphur fluoride and the products of degradation. This process used adsorbents when this gas is used as dielectric. The methodology employed was bibliography research, experimental design of the equipment, construction of the experimental equipment, selection and use of adsorbents, installation of the adsorption columns for the experimentation, flow of the sulfur hexafluoride through the adsorbents, searching of the fluoride hexafluoride before and after of the step through the adsorption columns and writing of the results. In base to the results we conclude that the process is good. The work could be advantage using chromatographic techniques with adequate standards. Is possible to extend the study using an additional number of adsorbents. (Author). 34 refs, 7 graphs, 3 tabs

  17. Uranium. Suppl. Vol. C7

    International Nuclear Information System (INIS)

    Keim, R.; Keller, C.

    1982-01-01

    In this supplement volume C7 the nitrogen compounds of uranium-anides, imides, nitrides, nitrites, nitrates are dealt with. Whereas amides, imides and nitrates have only been of scientific interest up to now, uranium nitride and uranylnitrate are of great technological importance. Therefore the description of the chemical and physical characteristics of UN as a potential fuel for future reactors already comprises about 1/4 of this volume. Also the description of uranyl nitrate - as one of the most important commercial forms of uranium and because of its importance in the chemistry of nuclear fuel element reprocessing - comprises many pages. This is supplemented by further uranium nitrides, ternary and polynary nitrides, oxide nitrides, double nitrides of the various valence steps as well as nitrate complexes and ternary and quarternary systems containing uranyl nitrate. The radiation behaviour of UN, and its distribution (liquid/liquid, liquid solid) as well as the complex formation of the uranyl ion with nitrate are described in other volumes of the uranium series. (RB) [de

  18. A roadmap to uranium ionic liquids: anti-crystal engineering.

    Science.gov (United States)

    Yaprak, Damla; Spielberg, Eike T; Bäcker, Tobias; Richter, Mark; Mallick, Bert; Klein, Axel; Mudring, Anja-Verena

    2014-05-19

    In the search for uranium-based ionic liquids, tris(N,N-dialkyldithiocarbamato)uranylates have been synthesized as salts of the 1-butyl-3-methylimidazolium (C4mim) cation. As dithiocarbamate ligands binding to the UO2(2+) unit, tetra-, penta-, hexa-, and heptamethylenedithiocarbamates, N,N-diethyldithiocarbamate, N-methyl-N-propyldithiocarbamate, N-ethyl-N-propyldithiocarbamate, and N-methyl-N-butyldithiocarbamate have been explored. X-ray single-crystal diffraction allowed unambiguous structural characterization of all compounds except N-methyl-N-butyldithiocarbamate, which is obtained as a glassy material only. In addition, powder X-ray diffraction as well as vibrational and UV/Vis spectroscopy, supported by computational methods, were used to characterize the products. Differential scanning calorimetry was employed to investigate the phase-transition behavior depending on the N,N-dialkyldithiocarbamato ligand with the aim to establish structure-property relationships regarding the ionic liquid formation capability. Compounds with the least symmetric N,N-dialkyldithiocarbamato ligand and hence the least symmetric anions, tris(N-methyl-N-propyldithiocarbamato)uranylate, tris(N-ethyl-N-propyldithiocarbamato)uranylate, and tris(N-methyl-N-butyldithiocarbamato)uranylate, lead to the formation of (room-temperature) ionic liquids, which confirms that low-symmetry ions are indeed suitable to suppress crystallization. These materials combine low melting points, stable complex formation, and hydrophobicity and are therefore excellent candidates for nuclear fuel purification and recovery. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  19. Operating conditions of T.B.P. line uranium purification plant, for uranium dioxide production

    International Nuclear Information System (INIS)

    Vardich, R.N.; La Gamma, A.M.; Anasco, R.; Soler, S.M.G. de; Isnardi, E.; Gea, V.; Chiaraviglio, R.; Matyjasczyk, E.; Aramayo, R.

    1992-01-01

    In this contribution are presented the operative conditions and the results obtained step of the Uranium dioxide production plant of Argentina. The refining step involve the Uranium concentrate dissolution, the silica ageing, the filtration and liquid - liquid extraction with n-tributyl phosphate solution in kerosene. The established operative conditions allow to obtain Uranyl nitrate solutions of nuclear purity in industrial scale. (author)

  20. Extraction of uranium(VI) by emulsion liquid membrane containing 5,8-diethyl-7-hydroxy-6-dodecanone oxime

    International Nuclear Information System (INIS)

    Akiba, Kenichi; Takahashi, Toshihiko; Kanno, Takuji

    1984-01-01

    Extraction of uranium(VI) by a liquid surfactant membrane has been studied. The stability of water-in-oil (w/o) emulsion dispersed in the continuous aqueous phase increased with an increase in surfactant concentrations and in the fraction of the organic phase in emulsion globules. Uranium(VI) in dilute acid solutions was extracted into (w/o) emulsions containing 5,8-diethyl-7-hydroxy-6-dodecanone oxime (LIX 63) as a mobile carrier and its concentration decreased according to [U]sub(t)=[U]sub(o)exp(-ksub(obsd)t). The apparent rate constants (ksub(obsd)) increased with an increase in carrier concentrations and in external pH values, while they were slightly dependent on the stripping acid concentrations. Uranium was transported and concentrated into the internal aqueous droplets. The final concentration of uranium in the external aqueous phase dropped to about 10 -3 of its initial value. (author)

  1. Study on treatment of radioactive liquid waste from uranium ore processing by the use of nano Fe_3O_4 KT particles

    International Nuclear Information System (INIS)

    Vuong Huu Anh; Nguyen Ba Tien; Doan Thi Thu Hien; Luu Cao Nguyen; Nguyen Van Chinh

    2015-01-01

    Nano Fe_3O_4 KT was produced from the Military Institute of Science and Technology were used to adsorbed heavy metal elements in liquid waste. In this report, the nano Fe_3O_4 KT particles sized 80-100 nm and specific surface area was 50-70 m"2/g was applied to study the adsorption of radioactive elements in the liquid waste of uranium ores processing. The effective parameters on adsorption process included temperature, stirring rate, stirring time, the pH value of the solution, the initial concentration of uranium in solution. The results showed the maximum adsorption capacity of the nano Fe_3O_4 KT was 53.5 mg/g with conditions such as room temperature, stirring speed 120 rounds/minute, the pH value of solution was 8, stirring time about 2 hours (Uranium/materials). From the results obtained, nano Fe_3O_4 KT tested to treatment liquid waste of uranium ore processing after preliminary precipitation removed almost heavy metals and a part of radioactive elements. The results were analyzed on the ICP-MS and α, β total counting, instrument. The solution concentration after treatment was suitable for Vietnam discharge standards into environment (QCVN 40:2011 on Industrial wastewater). (author)

  2. Microwave-assisted of dispersive liquid-liquid microextraction and spectrophotometric determination of uranium after optimization based on Box-Behnken design and chemometrics methods

    Science.gov (United States)

    Niazi, Ali; Khorshidi, Neda; Ghaemmaghami, Pegah

    2015-01-01

    In this study an analytical procedure based on microwave-assisted dispersive liquid-liquid microextraction (MA-DLLME) and spectrophotometric coupled with chemometrics methods is proposed to determine uranium. In the proposed method, 4-(2-pyridylazo) resorcinol (PAR) is used as a chelating agent, and chloroform and ethanol are selected as extraction and dispersive solvent. The optimization strategy is carried out by using two level full factorial designs. Results of the two level full factorial design (24) based on an analysis of variance demonstrated that the pH, concentration of PAR, amount of dispersive and extraction solvents are statistically significant. Optimal condition for three variables: pH, concentration of PAR, amount of dispersive and extraction solvents are obtained by using Box-Behnken design. Under the optimum conditions, the calibration graphs are linear in the range of 20.0-350.0 ng mL-1 with detection limit of 6.7 ng mL-1 (3δB/slope) and the enrichment factor of this method for uranium reached at 135. The relative standard deviation (R.S.D.) is 1.64% (n = 7, c = 50 ng mL-1). The partial least squares (PLS) modeling was used for multivariate calibration of the spectrophotometric data. The orthogonal signal correction (OSC) was used for preprocessing of data matrices and the prediction results of model, with and without using OSC, were statistically compared. MA-DLLME-OSC-PLS method was presented for the first time in this study. The root mean squares error of prediction (RMSEP) for uranium determination using PLS and OSC-PLS models were 4.63 and 0.98, respectively. This procedure allows the determination of uranium synthesis and real samples such as waste water with good reliability of the determination.

  3. Microwave-assisted of dispersive liquid-liquid microextraction and spectrophotometric determination of uranium after optimization based on Box-Behnken design and chemometrics methods.

    Science.gov (United States)

    Niazi, Ali; Khorshidi, Neda; Ghaemmaghami, Pegah

    2015-01-25

    In this study an analytical procedure based on microwave-assisted dispersive liquid-liquid microextraction (MA-DLLME) and spectrophotometric coupled with chemometrics methods is proposed to determine uranium. In the proposed method, 4-(2-pyridylazo) resorcinol (PAR) is used as a chelating agent, and chloroform and ethanol are selected as extraction and dispersive solvent. The optimization strategy is carried out by using two level full factorial designs. Results of the two level full factorial design (2(4)) based on an analysis of variance demonstrated that the pH, concentration of PAR, amount of dispersive and extraction solvents are statistically significant. Optimal condition for three variables: pH, concentration of PAR, amount of dispersive and extraction solvents are obtained by using Box-Behnken design. Under the optimum conditions, the calibration graphs are linear in the range of 20.0-350.0 ng mL(-1) with detection limit of 6.7 ng mL(-1) (3δB/slope) and the enrichment factor of this method for uranium reached at 135. The relative standard deviation (R.S.D.) is 1.64% (n=7, c=50 ng mL(-1)). The partial least squares (PLS) modeling was used for multivariate calibration of the spectrophotometric data. The orthogonal signal correction (OSC) was used for preprocessing of data matrices and the prediction results of model, with and without using OSC, were statistically compared. MA-DLLME-OSC-PLS method was presented for the first time in this study. The root mean squares error of prediction (RMSEP) for uranium determination using PLS and OSC-PLS models were 4.63 and 0.98, respectively. This procedure allows the determination of uranium synthesis and real samples such as waste water with good reliability of the determination. Copyright © 2014. Published by Elsevier B.V.

  4. Separation of uranium(VI) by liquid-solid extraction with tri-n-octylphosphine oxide diluted with naphthalene

    International Nuclear Information System (INIS)

    Shigetomi, Y.; Kojima, T.; Kamba, H.; Yamamoto, Y.

    1980-01-01

    Liquid-liquid distribution with tri-n-octylphosphine oxide (TOPO) and molten naphthalene has been investigated for the extraction of 20 metals from nitric acid and hydrochloric acid solutions. Uranium is quantitatively extracted from 1 M nitric acid or hydrochloric acid by using 100 mg of TOPO and 200 mg of naphthalene and shaking for 5 min at 80 0 C, and separated from transition metals, alkaline earth metals and rare earth metals (except scandium). Addition of naphthalene increases the extraction efficiency. (Auth.)

  5. Standard test method for determination of impurities in nuclear grade uranium compounds by inductively coupled plasma mass spectrometry

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2010-01-01

    1.1 This test method covers the determination of 67 elements in uranium dioxide samples and nuclear grade uranium compounds and solutions without matrix separation by inductively coupled plasma mass spectrometry (ICP-MS). The elements are listed in Table 1. These elements can also be determined in uranyl nitrate hexahydrate (UNH), uranium hexafluoride (UF6), triuranium octoxide (U3O8) and uranium trioxide (UO3) if these compounds are treated and converted to the same uranium concentration solution. 1.2 The elements boron, sodium, silicon, phosphorus, potassium, calcium and iron can be determined using different techniques. The analyst's instrumentation will determine which procedure is chosen for the analysis. 1.3 The test method for technetium-99 is given in Annex A1. 1.4 The values stated in SI units are to be regarded as standard. 1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish ...

  6. Analytical method of uranium (IV) and uranium (VI) in uranium ores and uranium-bearing rocks

    International Nuclear Information System (INIS)

    Shen Zhuqin; Zheng Yongfeng; Li Qingzhen; Zhong Miaolan; Gu Dingxiang

    1995-11-01

    The best conditions for keeping the original valences of uranium during the dissolution and separation procedure of geological samples (especially those micro uranium-bearing rock) were studied. With the exist of high concentration protectants, the sample was decomposed with concentration HF at 40 +- 5 degree C. The U(VI) was dissolved completely and formed stable complex UO 2 F 2 , the U(IV) was precipitated rapidly and carried by carrier. Quantitative separation was carried out immediately with suction. The decomposition of sample and separation of solid/liquid phases was completed within two minutes. After separation, the U(IV) and U(VI) were determined quantitatively with laser fluorescence or voltametry respectively according to the uranium content. The limit of detection for this method is 0.7 μg/g, RSD is 10.5%, the determinate range of uranium is 2 x 10 -6 ∼10 -1 g/g. The uranium contents and their valence state ratio were measured for more than one hundred samples of sand stone and granite, the accuracy and precision of these results are satisfactory for uranium geological research. (12 tabs.; 11 refs.)

  7. Contribution to the study of the new international philosophy of the radiological safety in the natural uranium chemical treatment

    International Nuclear Information System (INIS)

    Moraes da Silva, T. de

    1990-01-01

    The objective of this work is to adapt the Radiological Safety System in the facilities concerned to the chemical treatment of the uranium concentrated (yellow-cake) until conversion in uranium hexafluoride in the pilot plant of IPEN-CNEN/SP, to the new international philosophy adopted by ICRP and IAEA. The new philosophy changes fully the Radiological Protection concepts of preceding philosophy, changes, also, the concept of the workplace and individual monitoring as well as the classification of the working areas. In this paper we show the monitoring program, in each phase of the natural uranium treatment chemical process in conversion facility for external irradiation, surface contamination and air contamination. The results were analysed according with the new philosophy and used to reclassify the workplace. It was introduced the condition work concept taking account the time spent by the worker in that workplace. (author)

  8. Processing of stored uranium tetrafluoride for productive use

    International Nuclear Information System (INIS)

    Whinnery, W.N. III

    1987-01-01

    Waste uranium tetrafluoride (UF4) was created from converting uranium hexafluoride (UF6) to UF4 for generation of hydrogen fluoride. This resulted in more tails cylinders being made available in the early days of the Paducah Gaseous Diffusion Plant. A need arose for the UF4; however, a large portion of the material was stored outside in 55-gallon drums where the material became caked and very hard. Chemical operations crushed, ground, and screened a large portion of the waste UF4 from 1981-1987. Over 111,935,000 pounds of the material has been processed and put into productive use at Westinghouse Materials Company of Ohio or at Department of Defense facilities. This long-term effort saved the disposal cost of the material which is estimated at $9,327,900. In addition, the work was for an outside contract which lowered the operating cost of the Chemical Operations Department by $4,477,400. Disposal options for the material still present in the current inventory are outlined

  9. A roadmap to uranium ionic liquids: Anti-crystal engineering

    Energy Technology Data Exchange (ETDEWEB)

    Yaprak, Damla; Spielberg, Eike T.; Baecker, Tobias; Richter, Mark; Mallick, Bert [Inorganic Chemistry III, Ruhr-University Bochum (Germany); Klein, Axel [Institut fuer Anorganische Chemie, Koeln Univ. (Germany); Mudring, Anja-Verena [Inorganic Chemistry III, Ruhr-University Bochum (Germany); Materials Science and Engineering, Iowa State University and Critical Materials Institute, Ames Laboratory, Ames, IA (United States)

    2014-05-19

    In the search for uranium-based ionic liquids, tris(N,N-dialkyldithiocarbamato)uranylates have been synthesized as salts of the 1-butyl-3-methylimidazolium (C{sub 4}mim) cation. As dithiocarbamate ligands binding to the UO{sub 2}{sup 2+} unit, tetra-, penta-, hexa-, and heptamethylenedithiocarbamates, N,N-diethyldithiocarbamate, N-methyl-N-propyldithiocarbamate, N-ethyl-N-propyldithiocarbamate, and N-methyl-N-butyldithiocarbamate have been explored. X-ray single-crystal diffraction allowed unambiguous structural characterization of all compounds except N-methyl-N-butyldithiocarbamate, which is obtained as a glassy material only. In addition, powder X-ray diffraction as well as vibrational and UV/Vis spectroscopy, supported by computational methods, were used to characterize the products. Differential scanning calorimetry was employed to investigate the phase-transition behavior depending on the N,N-dialkyldithiocarbamato ligand with the aim to establish structure-property relationships regarding the ionic liquid formation capability. Compounds with the least symmetric N,N-dialkyldithiocarbamato ligand and hence the least symmetric anions, tris(N-methyl-N-propyldithiocarbamato)uranylate, tris(N-ethyl-N-propyldithiocarbamato)uranylate, and tris(N-methyl-N-butyldithiocarbamato)uranylate, lead to the formation of (room-temperature) ionic liquids, which confirms that low-symmetry ions are indeed suitable to suppress crystallization. These materials combine low melting points, stable complex formation, and hydrophobicity and are therefore excellent candidates for nuclear fuel purification and recovery. (copyright 2014 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  10. A roadmap to uranium ionic liquids: Anti-crystal engineering

    International Nuclear Information System (INIS)

    Yaprak, Damla; Spielberg, Eike T.; Baecker, Tobias; Richter, Mark; Mallick, Bert; Klein, Axel; Mudring, Anja-Verena

    2014-01-01

    In the search for uranium-based ionic liquids, tris(N,N-dialkyldithiocarbamato)uranylates have been synthesized as salts of the 1-butyl-3-methylimidazolium (C_4mim) cation. As dithiocarbamate ligands binding to the UO_2"2"+ unit, tetra-, penta-, hexa-, and heptamethylenedithiocarbamates, N,N-diethyldithiocarbamate, N-methyl-N-propyldithiocarbamate, N-ethyl-N-propyldithiocarbamate, and N-methyl-N-butyldithiocarbamate have been explored. X-ray single-crystal diffraction allowed unambiguous structural characterization of all compounds except N-methyl-N-butyldithiocarbamate, which is obtained as a glassy material only. In addition, powder X-ray diffraction as well as vibrational and UV/Vis spectroscopy, supported by computational methods, were used to characterize the products. Differential scanning calorimetry was employed to investigate the phase-transition behavior depending on the N,N-dialkyldithiocarbamato ligand with the aim to establish structure-property relationships regarding the ionic liquid formation capability. Compounds with the least symmetric N,N-dialkyldithiocarbamato ligand and hence the least symmetric anions, tris(N-methyl-N-propyldithiocarbamato)uranylate, tris(N-ethyl-N-propyldithiocarbamato)uranylate, and tris(N-methyl-N-butyldithiocarbamato)uranylate, lead to the formation of (room-temperature) ionic liquids, which confirms that low-symmetry ions are indeed suitable to suppress crystallization. These materials combine low melting points, stable complex formation, and hydrophobicity and are therefore excellent candidates for nuclear fuel purification and recovery. (copyright 2014 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  11. Uranium chemistry: significant advances

    International Nuclear Information System (INIS)

    Mazzanti, M.

    2011-01-01

    The author reviews recent progress in uranium chemistry achieved in CEA laboratories. Like its neighbors in the Mendeleev chart uranium undergoes hydrolysis, oxidation and disproportionation reactions which make the chemistry of these species in water highly complex. The study of the chemistry of uranium in an anhydrous medium has led to correlate the structural and electronic differences observed in the interaction of uranium(III) and the lanthanides(III) with nitrogen or sulfur molecules and the effectiveness of these molecules in An(III)/Ln(III) separation via liquid-liquid extraction. Recent work on the redox reactivity of trivalent uranium U(III) in an organic medium with molecules such as water or an azide ion (N 3 - ) in stoichiometric quantities, led to extremely interesting uranium aggregates particular those involved in actinide migration in the environment or in aggregation problems in the fuel processing cycle. Another significant advance was the discovery of a compound containing the uranyl ion with a degree of oxidation (V) UO 2 + , obtained by oxidation of uranium(III). Recently chemists have succeeded in blocking the disproportionation reaction of uranyl(V) and in stabilizing polymetallic complexes of uranyl(V), opening the way to to a systematic study of the reactivity and the electronic and magnetic properties of uranyl(V) compounds. (A.C.)

  12. Performance of the mesh-type liquid cadmium cathode structure for the electrodeposition of uranium from the molten salt

    International Nuclear Information System (INIS)

    Paek, S.; Kim, S.H.; Lee, H.; Ahn, D.H.; Yoon, D.S.

    2010-01-01

    A mesh-type liquid cadmium cathode (LCC) structure has been devised to improve the performance of the electro-winning process for the recovery of actinides in a molten chloride system. For the verification of its performance, electrodeposition experiments of uranium from the molten LiCl-KCl-UCl 3 salt were conducted at 773 K for different current densities using the mesh-type LCC structure. Uranium was successfully collected over 5 wt. % in the LCC without growing uranium dendrites. The mesh-type LCC structure prevented the uncontrolled growth of uranium dendrites into the electrolyte phase above the cadmium surface and caused the LCC deposit to accumulate at the higher in the cadmium phase over uranium solubility in cadmium. After cooling the LCC crucible, its solid deposits were identified as an intermetallic compound UCd 11 by EPMA and XRD analysis. The cathode potential profiles from the electrochemical experiments and the chemical structure of the LCC deposits showed that it could be applied practically to recover the actinides above their solubility in cadmium. (orig.)

  13. Phosphorus and uranium recovery process from phosphated rocks

    Energy Technology Data Exchange (ETDEWEB)

    Sze, M C.Y.; Long, R H

    1981-01-30

    Improvement of uranium recovery in phosphate rocks by treatment with nitric acid avoiding the formation of a precipitate including a part of the uranium. The separation of uranium from phosphoric acid is obtained by liquid-liquid extraction using dialkyl posphoric acid with at least 10 carbon atoms and a phosphoryl alkyl alkoxy compound with at least 10 carbon atoms and a non water miscible organic solvent.

  14. Determination of the isotopic ratio 235U/238U in UF6 using quadrupole mass spectrometry

    International Nuclear Information System (INIS)

    Kusahara, Helena Sueco

    1979-01-01

    In this work measurements of isotope ratios 235 U / 23 '8U in uranium hexafluoride are carried out using a quadrupole mass spectrometer. The operational parameters, which affect the final precision of the results, are standardized. Optimized procedures for the preparation of uranium hexafluoride samples by fluorination of uranium oxides using cobalt trifluoride method are established. Careful attention is given to the process of purification of uranium hexafluoride samples by fractional distillation. Adequate statistical methods for analysing the results obtained for single ratio measurements as well as the ratio ' of isotopic ratios of sample and standard ar.e developed. A precision of about 10 -4 for single ratio measurements and accuracy of about 0,3% for the ratio of sample and standard ratios are obtained. These results agree with the values which have been obtained using magnetic mass spectrometers. The procedures and methods established in this work can be employed in the systematic uranium isotope analysis in UF 6 form. (author)

  15. Carbon diffusion in molten uranium: an ab initio molecular dynamics study

    Science.gov (United States)

    Garrett, Kerry E.; Abrecht, David G.; Kessler, Sean H.; Henson, Neil J.; Devanathan, Ram; Schwantes, Jon M.; Reilly, Dallas D.

    2018-04-01

    In this work we used ab initio molecular dynamics within the framework of density functional theory and the projector-augmented wave method to study carbon diffusion in liquid uranium at temperatures above 1600 K. The electronic interactions of carbon and uranium were described using the local density approximation (LDA). The self-diffusion of uranium based on this approach is compared with literature computational and experimental results for liquid uranium. The temperature dependence of carbon and uranium diffusion in the melt was evaluated by fitting the resulting diffusion coefficients to an Arrhenius relationship. We found that the LDA calculated activation energy for carbon was nearly twice that of uranium: 0.55 ± 0.03 eV for carbon compared to 0.32 ± 0.04 eV for uranium. Structural analysis of the liquid uranium-carbon system is also discussed.

  16. Overview of toxicity data and risk assessment methods for evaluating the chemical effects of depleted uranium compounds

    International Nuclear Information System (INIS)

    Hartmann, H.M.; Monette, F.A.; Avci, H.I.

    2000-01-01

    In the United States, depleted uranium is handled or used in several chemical forms by both governmental agencies and private industry (primarily companies producing and machining depleted uranium metal for military applications). Human exposure can occur as a result of handling these compounds, routine low-level effluent releases to the environment from processing facilities, or materials being accidentally released from storage locations or during processing or transportation. Exposure to uranium can result in both chemical and radiological toxicity, but in most instances chemical toxicity is of greater concern. This article discusses the chemical toxic effects from human exposure to depleted uranium compounds that are likely to be handled during the long-term management and use of depleted uranium hexafluoride (UF 6 ) inventories in the United States. It also reviews representative publications in the toxicological literature to establish appropriate reference values for risk assessments. Methods are described for evaluating chemical toxicity caused by chronic low-level exposure and acute exposure. Example risk evaluations are provided for illustration. Preliminary results indicate that chemical effects of chronic exposure to uranium compounds under normal operating conditions would be negligibly small. Results also show that acute exposures under certain accident conditions could cause adverse chemical effects among the populations exposed.

  17. Uranium dioxide in Fe(III)-containing ionic liquids with DMSO: Dissolution, separation, and structural characterization

    Energy Technology Data Exchange (ETDEWEB)

    Yao, Aining; Chu, Taiwei, E-mail: twchu@pku.edu.cn

    2016-11-15

    UO{sub 2} can be successfully dissolved in imidazolium-based Fe(III)-containing ionic liquids (ILs) with the help of DMSO. Spectroscopic studies and X-ray diffraction show that UO{sub 2}Cl{sub 4}{sup 2−} is the principal product. The dissolved uranyl species can be easily separated from the ILs via a combination of crystallization and solvent extraction. Moreover, even if 15.2 wt% of the rare-earth elements of Sm, Eu, and Gd, compared with the total amount of uranium and the rare-earth elements, exist in the IL, only uranium-containing crystals would be selectively formed and separated from the system. The solvents of acetone and acetonitrile could be used to separate the rare-earth elements from uranium in the IL with the help of imidazolium chloride. Considering the complete process from the dissolution of UO{sub 2} and some rare-earth oxides to the separation of uranium and rare-earth elements in the IL, the facile approach is promising for the spent nuclear fuel reprocessing. - Graphical abstract: UO{sub 2} can be successfully dissolved in Fe-containing ILs with the help of DMSO to form UO{sub 2}Cl{sub 4}{sup 2−}. The rare earth elements of Sm, Eu, and Gd can be separated from uranium in the IL, and meanwhile, the recovery of dissolved uranyl species and Fe-containing IL can also be achieved. - Highlights: • Dissolution of UO{sub 2} can be successfully achieved in imidazolium-based Fe-containing ILs with the help of DMSO without additional oxidants. • Compared with the total amount of uranium and the rare-earth elements, even if 15.2 wt% of the rare-earth elements of Sm, Eu, and Gd exist in the IL, only uranium-containing crystals would be selectively formed and separated from the system. • The separation of the rare-earth elements from uranium has also been achieved via a combination of crystallization and solvent extraction.

  18. Uranium dioxide in Fe(III)-containing ionic liquids with DMSO: Dissolution, separation, and structural characterization

    International Nuclear Information System (INIS)

    Yao, Aining; Chu, Taiwei

    2016-01-01

    UO_2 can be successfully dissolved in imidazolium-based Fe(III)-containing ionic liquids (ILs) with the help of DMSO. Spectroscopic studies and X-ray diffraction show that UO_2Cl_4"2"− is the principal product. The dissolved uranyl species can be easily separated from the ILs via a combination of crystallization and solvent extraction. Moreover, even if 15.2 wt% of the rare-earth elements of Sm, Eu, and Gd, compared with the total amount of uranium and the rare-earth elements, exist in the IL, only uranium-containing crystals would be selectively formed and separated from the system. The solvents of acetone and acetonitrile could be used to separate the rare-earth elements from uranium in the IL with the help of imidazolium chloride. Considering the complete process from the dissolution of UO_2 and some rare-earth oxides to the separation of uranium and rare-earth elements in the IL, the facile approach is promising for the spent nuclear fuel reprocessing. - Graphical abstract: UO_2 can be successfully dissolved in Fe-containing ILs with the help of DMSO to form UO_2Cl_4"2"−. The rare earth elements of Sm, Eu, and Gd can be separated from uranium in the IL, and meanwhile, the recovery of dissolved uranyl species and Fe-containing IL can also be achieved. - Highlights: • Dissolution of UO_2 can be successfully achieved in imidazolium-based Fe-containing ILs with the help of DMSO without additional oxidants. • Compared with the total amount of uranium and the rare-earth elements, even if 15.2 wt% of the rare-earth elements of Sm, Eu, and Gd exist in the IL, only uranium-containing crystals would be selectively formed and separated from the system. • The separation of the rare-earth elements from uranium has also been achieved via a combination of crystallization and solvent extraction.

  19. Removal of Radioactive Pollutants by Liquid Emulsion Membrane From Liquid Waste

    International Nuclear Information System (INIS)

    Yossef, Y.A.A.

    2013-01-01

    Radioactive liquid waste should be safely managed because it is potentially hazardous to human health and the environment. Several methods were used for treatment of liquid waste, such as liquid emulsion membrane (LEM). In this work, liquid emulsion membrane using Tri-butyl phosphate (TBP) plus Bis (2-ethylhexyl) phosphate (HDEHP) as mobile carriers, hydrochloric acid (HCl) as stripping agents and an emulsifying agent (span 80) was used for the extraction of uranium ions from radioactive liquid waste. Various parameters influencing the permeation of uranium ions through the membrane have been optimized to separate uranium ions from radioactive liquid waste such as: the effects of membrane material, carrier concentration, operating conditions, etc. were examined; moreover, the transport mechanism of this uranium was also studied. The internal mass transfer in the water/oil (W/O) emulsion drop, the external mass transfer around the drop, the rates of formation, and the decomposition of the complex at the external aqueous-organic interface were considered. The results show that, the liquid emulsion membrane which consists of (25% by volume HDEHP, 0.005 M + 75% by volume TBP, 0.01 M) as extractant (carrier), span 80, 4% (v/v) (sorbitan monooleate) as surfactant agent, hydrochloric acid (HCl), (1.0 M) as stripping agent. From the results, the maximum extraction percent of uranium ions (nearly about of 100%) occurred at the operating conditions: stirring speed =500 rpm, the ratio between LEM and feed phase (liquid waste) = 20 ml: 100 ml, the ratio between organic phase (membrane phase) to internal aqueous phase (stripping phase) = 1.0 and the ph value of the external aqueous phase equal to 5.0.

  20. Isotope separation using vibrationally excited molecules

    International Nuclear Information System (INIS)

    Woodroffe, J.A.; Keck, J.C.

    1977-01-01

    A system for isotope separation or enrichment wherein molecules of a selected isotope type in a flow of molecules of plural isotope types are vibrationally excited and collided with a background gas to provide enhanced diffusivity for the molecules of the selected isotope type permitting their separate collection. The system typically is for the enrichment of uranium using a uranium hexafluoride gas in combination with a noble gas such as argon. The uranium hexafluoride molecules having a specific isotope of uranium are vibrationally excited by laser radiation. The vibrational energy is converted to a translation energy upon collision with a particle of the background gas and the added translation energy enhances the diffusivity of the selected hexafluoride molecules facilitating its condensation on collection surfaces provided for that purpose. This process is periodically interrupted and the cryogenic flow halted to permit evaporation of the collected molecules to provide a distinct, enriched flow

  1. Uranium recovery from wet process phosphoric acid

    International Nuclear Information System (INIS)

    Carrington, O.F.; Pyrih, R.Z.; Rickard, R.S.

    1981-01-01

    Improvement in the process for recovering uranium from wetprocess phosphoric acid solution derived from the acidulation of uraniferous phosphate ores by the use of two ion exchange liquidliquid solvent extraction circuits in which in the first circuit (A) the uranium is reduced to the uranous form; (B) the uranous uranium is recovered by liquid-liquid solvent extraction using a mixture of mono- and di-(Alkyl-phenyl) esters of orthophosphoric acid as the ion exchange agent; and (C) the uranium oxidatively stripped from the agent with phosphoric acid containing an oxidizing agent to convert uranous to uranyl ions, and in the second circuit (D) recovering the uranyl uranium from the strip solution by liquid-liquid solvent extraction using di(2ethylhexyl)phosphoric acid in the presence of trioctylphosphine oxide as a synergist; (E) scrubbing the uranium loaded agent with water; (F) stripping the loaded agent with ammonium carbonate, and (G) calcining the formed ammonium uranyl carbonate to uranium oxide, the improvement comprising: (1) removing the organics from the raffinate of step (B) before recycling the raffinate to the wet-process plant, and returning the recovered organics to the circuit to substantially maintain the required balance between the mono and disubstituted esters; (2) using hydogren peroxide as the oxidizing agent in step (C); (3) using an alkali metal carbonate as the stripping agent in step (F) following by acidification of the strip solution with sulfuric acid; (4) using some of the acidified strip solution as the scrubbing agent in step (E) to remove phosphorus and other impurities; and (5) regenerating the alkali metal loaded agent from step (F) before recycling it to the second circuit

  2. Extraction of Uranium from Aqueous Solutions Using Ionic Liquid and Supercritical Carbon Dioxide in Conjunction

    International Nuclear Information System (INIS)

    Wang, Joanna S.; Sheaff, Chrystal N.; Yoon, Byunghoon; Addleman, Raymond S.; Wai, Chien M.

    2009-01-01

    Uranyl ions (UO2)2+ in aqueous nitric acid solutions can be extracted into supercritical CO2 (sc-CO2) via an imidazolium-based ionic liquid using tri-n-butylphosphate (TBP) as a complexing agent. The transfer of uranium from the ionic liquid to the supercritical fluid phase was monitored by UV/Vis spectroscopy using a high-pressure fiberoptic cell. The form of the uranyl complex extracted into the supercritical CO2 phase was found to be UO2(NO3)2(TBP)2. The extraction results were confirmed by UV/Vis spectroscopy and by neutron activation analysis. This technique could potentially be used to extract other actinides for applications in the field of nuclear waste management.

  3. Application of supported liquid membranes for removal of uranium from groundwater

    International Nuclear Information System (INIS)

    Chiarizia, R.; Horwitz, E.P.; Rickert, P.G.; Hodgson, K.M.

    1989-01-01

    The separation of uranium from Hanford site groundwater as studied by hollow-fiber supported liquid membranes, SLM. The carrier bis(2,4,4-trimethylpentyl)phosphinic acid, H[DTMPep], contained in the commercial extractant Cyanex trademark 272 was used as a membrane carrier, because of its selectivity for U over calcium and magnesium. The water soluble complexing agent, 1-hydroxyethane-1,1-diphosphonic acid, HEDPA, was used as stripping agent. Polypropylene hollow-fibers and n-dodecane were used as polymeric support and diluent, respectively. Laboratory scale hollow-fiber modules were employed in a recycling mode, using as feed synthetic groundwater at pH 2, to confirm the capability of the proposed SLM system to separate and concentrate U(VI) in the strip solution. Information was obtained on the U(VI) concentration factor and on the long-term performance of the SLMs. Encouraging results were obtained both with a conventional module and with a module containing a carrier solution reservoir. Industrial scale modules were used at Hanford to test the SLM separation of U(VI) from real contaminated groundwater. The uranium concentration was reduced from approximately 3500 ppB to about 1 ppB in a few hours. 9 refs., 8 figs., 4 tabs

  4. Liver metastases: Sulphur hexafluoride-enhanced ultrasonography for lesion detection: a systematic review

    NARCIS (Netherlands)

    Cabassa, Paolo; Bipat, Shandra; Longaretti, Laura; Morone, Mario; Maroldi, Roberto

    2010-01-01

    This is a systematic review to evaluate the accuracy of contrast-enhanced ultrasonography (CEUS) performed with "SonoVue" (sulphur hexafluoride) in the detection of hepatic metastases. The MEDLINE, EMBASE and COCHRANE Databases were searched, regardless of language, for relevant articles published

  5. Development of solid materials for UF6 sampling: FY16 Annual Report

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Nicholas [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Savina, Joseph [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Hebden, Andrew [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division

    2016-10-31

    A handheld implementation of the ABACC-developed Cristallini method, which captures uranium hexafluoride samples as an inert salt, was organized in FY17 and succeeded in demonstrating the handheld sampler concept with reactive hexafluoride gases. The Cristallini method relies on the use of a hydrated substrate to react the incoming hexafluoride resulting in the formation of a stable uranyl fluoride salt. The Cristallini method has been demonstrated as a facility modification installed near the sampling tap of a gas centrifuge enrichment plant. While very successful in reducing the hazards of uranium hexafluoride sample, the method still takes a considerable amount of time and can only be used in facilities where the apparatus has been installed; this arrangement generally prohibits the sampling of filled cylinders that have already exited the facility and have been deposited in the on-site tank storage yard. The handheld unit under development will allow the use of the Cristallini method at facilities that have not been converted as well as tanks in the storage yard. The handheld system utilizes an active vacuum system, rather than a passive vacuum system in the facility setup, to drive the uranium hexafluoride onto the adsorbing media. The handheld unit will be battery operated for fully autonomous operation and will include onboard pressure sensing and flushing capability. To date, the system concept of operations was demonstrated with tungsten hexafluoride that showed the active vacuum pump with multiple cartridges of adsorbing media was viable. Concurrently, the hardened prototype system was developed and tested; removable sample cartridges were developed (the only non-COTS component to date); and preparations were made for uranium tests and a domestic field test.

  6. Method of separation of uranium from contaminating ions in an aqueous feed liquid containing uranyl ions

    International Nuclear Information System (INIS)

    Sundar, P.S.; Elikan, L.; Lyon, W.L.

    1975-01-01

    A coupled cationic/anionic method for the separation of uranium from contaminated aqueous solutions which contain uranyl ions is proposed. The fluid is extracted using an organic solvent containing a reagent which, together with the uranyl ions, forms a soluble aggregate in that solvent. As an example, 0.1 - 1 Mol/l Di-2-ethyl-hexyl-phosphorous acid in kerosene is mentioned. The organic solvent is then treated with a sealing liquid (volume ratio 20 - 35). For separation, an aqueous carbonate solution or a sulfuric acid solution can be used; the most favorable pH-values and concentrations for both cases are mentioned. The U +4 -ion at the sulfuric acid separation is subsequently oxidized to the uranyl ion with air. In each case, an extraction with an amine follows; after that, the amine is separated using an ammonium-carbonate solution and the uranium aggregate is precipitated, for example as ammonium uranyl tricarbonate, and then further processed to uranium oxide. The solvents and fluids used are led back in closed circuit; a flow diagram is given. (UWI) [de

  7. The extraction of uranium from wet process phosphoric acid using a liquid surfactant membrane system

    International Nuclear Information System (INIS)

    Dickens, N.; Davies, G.A.

    1984-01-01

    A liquid membrane extraction process is examined for the extraction of uranium from wet process phosphoric acid. Uranium is present in the acid in concentrations up to 100 ppm which in principle makes it ideal for treatment with a membrane process. The membrane system studied is based on extraction using DEHPA-TOPO reagents which are contained within the organic phase of a water in oil emulsion. Formulations of the emulsion membrane system have been studied, the limitations of acid temperature, P 2 O 5 concentration and solid dispersed impurities in the acid have been studied in laboratory batch experiments and in a continuous pilot plant unit capable of treating 5l of concentrated acid per minute. Data from the pilot plant work has been used to develop a flowsheet for a commercial unit based on this process. (author)

  8. The TRUEX [TRansUranium EXtraction] process and the management of liquid TRU [transuranic] waste

    International Nuclear Information System (INIS)

    Schulz, W.W.; Horwitz, E.P.

    1987-01-01

    The TRUEX process is a new generic liquid-liquid extraction process for removal of all actinides from acidic nitrate or chloride nuclear waste solutions. Because of its high efficiency and great flexibility, the TRUEX process appears destined to be widely used in the US and possibly in other countries for cost-effective management and disposal of transuranic (TRU) wastes. In the US, TRU wastes are those that contain ≥3.7 x 10 6 Bq/kg) of TRU elements with half-lives greater than 20 y. This paper gives a brief review of the relevant chemistry and summarizes the current status of development and deployment of the TRUEX (TRansUranium EXtraction) process flowsheets to treat specific acidic waste solutions at several US Department of Energy sites. 19 refs., 4 figs., 4 tabs

  9. Kinetics of low pressure chemical vapor deposition of tungsten silicide from dichlorocilane reduction of tungsten hexafluoride

    International Nuclear Information System (INIS)

    Srinivas, D.; Raupp, G.B.; Hillman, J.

    1990-01-01

    The authors report on experiments to determine the intrinsic surface reaction rate dependences and film properties' dependence on local reactant partial pressures and wafer temperature in low pressure chemical vapor deposition (LPCVD) of tungsten silicide from dichlorosilane reduction of tungsten hexafluoride. Films were deposited in a commercial-scale Spectrum CVD cold wall single wafer reactor under near differential, gradientless conditions. Over the range of process conditions investigated, deposition rate was found to be first order in dichlorosillane and negative second order in tungsten hexafluoride partial pressure. The apparent activation energy in the surface reaction limited regime was found to be 70-120 kcal/mol. The silicon to tungsten ratio of as deposited silicide films ranged from 1.1 to 2.4, and increased with increasing temperature and dichlorosillane partial pressure, and decreased with increasing tungsten hexafluoride pressure. These results suggest that the apparent silicide deposition rate and composition are controlled by the relative rates of at least two competing reactions which deposit stoichiometric tungsten silicides and/or silicon

  10. Determination of uranium and thorium in complex matrices by two solvent extraction separation techniques and photon electron rejecting alpha liquid spectrometry

    International Nuclear Information System (INIS)

    Ayranov, M.; Wacker, L.; Kraehenbuehl, U.

    2001-01-01

    The separation of uranium and thorium from complex matrixes such as marine sediments using solvent extraction and determination by means of photon-electron rejecting liquid alpha spectrometry (PERALS trademark) has successfully been performed. Two extraction schemes, using TOPO and HDEHP, respectively, were compared for the separation of uranium and thorium from the matrix components. The results show recoveries between 73 and 92% for 234 U, 238 U, 232 Th, 230 Th and 238 Th with an accuracy of the methods ±12%. Minimum detectable activities for counting time up to 500 000 seconds for 0.5 g sample material were between 0.34-1.15 Bq/kg for uranium and 0.31-1.66 Bq/kg for thorium. (orig.)

  11. Nuclear Science and Technology Branch report 1977

    International Nuclear Information System (INIS)

    Hardy, C.J.

    1977-12-01

    A report of research programs continuing in the following areas is presented: mining and treatment of uranium ores, manufacture of uranium hexafluoride, uranium enrichment, waste treatment, reprocessing and the uranium fuel cycle. Staff responsible for each project are indicated

  12. Measurements of the thermal radiative properties of liquid uranium

    International Nuclear Information System (INIS)

    Havstad, M.A.; McLean, W. II; Self, S.A.

    1992-07-01

    Measurements of the thermal radiative properties of liquid uranium have been made using an instrument with two optical systems, one for measuring the complex index of refraction by ellipsometry, the other for measuring the normal spectral emissivity by direct comparison to an integral blackbody cavity. The measurements cover the wavelength range 0.4 to 10 μm with sample temperatures between 940 and 1630 K. Two 5keV ion sputter guns and an Auger spectrometer produce and verify, in-situ, atomically pure sample surfaces. Good agreement between the two methods is observed for the normal spectral emissivity, which varies with wavelength in a manner typical of transition metals. The two components of the complex index of refraction, the index of refraction and the extinction coefficient, increase with wavelength, from ∼3 at 0.4 μm to -20 at 9.5 μm. Both components of polarized reflectivity are shown for visible to infrared wavelengths

  13. Supercritical fluid extraction of uranium

    International Nuclear Information System (INIS)

    Kumar, Pradeep

    2017-01-01

    Uranium being strategic material, its separation and purification is of utmost importance in nuclear industry, for which solvent extraction is being employed. During solvent extraction significant quantity of radioactive liquid waste gets generated which is of environmental concern. In recent decades supercritical fluid extraction (SFE) has emerged as promising alternative to solvent extraction owing to its inherent advantage of reduction in liquid waste generation and simplification of process. In this paper a brief overview of research work carried out so far on SFE of uranium by BARC has been given

  14. Salt Removal from the Uranium Deposits of Electrorefiner

    Energy Technology Data Exchange (ETDEWEB)

    Kwon, S. W.; Park, K. M.; Lee, S. J.; Park, S. B.; Cho, C. H.; Choi, S. Y.; Lee, H. S.; Kim, J. G. [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2010-10-15

    Electrorefining is a key step in pyroprocessing. The electrorefining process is generally composed of two recovery steps. The deposit of uranium onto a solid cathode and the recovery of the remaining uranium and TRU elements simultaneously by a liquid cadmium cathode. The solid cathode processing is necessary to separate the salt from the cathode since the uranium deposit in a solid cathode contains electrolyte salt. In the liquid cathode, cadmium metal should be removed to recover actinide product. A physical separation process, such as distillation separation, is more attractive than a chemical or dissolution process because physical processes generate much less secondary process. Distillation process was employed for the cathode processing due to the advantages of minimal generation of secondary waste, compact unit process, simple and low cost equipment. The basis for vacuum distillation separation is the difference in vapor pressures between salt and uranium. A solid cathode deposit is heated in a heating region and salt vaporizes, while non volatile uranium remains behind. It is very important to increase the throughput of the salt separation system due to the high uranium content of spent nuclear fuel and high salt fraction of uranium dendrites. The evaporation rate of the LiCl-KCl eutectic salt in vacuum distiller is not so high to come up with the generation capacity of uranium dendrites in electro-refiner. Therefore, wide evaporation area or high distillation temperature is necessary for the successful salt separation. In this study, the solid-liquid separation was proposed prior to distillation of salt and a feasibility of the separation of the liquid salt by a metallic wire mesh (sieve) was tested for the reduction of the burden of the following vacuum distillation process

  15. Salt Removal from the Uranium Deposits of Electrorefiner

    International Nuclear Information System (INIS)

    Kwon, S. W.; Park, K. M.; Lee, S. J.; Park, S. B.; Cho, C. H.; Choi, S. Y.; Lee, H. S.; Kim, J. G.

    2010-01-01

    Electrorefining is a key step in pyroprocessing. The electrorefining process is generally composed of two recovery steps. The deposit of uranium onto a solid cathode and the recovery of the remaining uranium and TRU elements simultaneously by a liquid cadmium cathode. The solid cathode processing is necessary to separate the salt from the cathode since the uranium deposit in a solid cathode contains electrolyte salt. In the liquid cathode, cadmium metal should be removed to recover actinide product. A physical separation process, such as distillation separation, is more attractive than a chemical or dissolution process because physical processes generate much less secondary process. Distillation process was employed for the cathode processing due to the advantages of minimal generation of secondary waste, compact unit process, simple and low cost equipment. The basis for vacuum distillation separation is the difference in vapor pressures between salt and uranium. A solid cathode deposit is heated in a heating region and salt vaporizes, while non volatile uranium remains behind. It is very important to increase the throughput of the salt separation system due to the high uranium content of spent nuclear fuel and high salt fraction of uranium dendrites. The evaporation rate of the LiCl-KCl eutectic salt in vacuum distiller is not so high to come up with the generation capacity of uranium dendrites in electro-refiner. Therefore, wide evaporation area or high distillation temperature is necessary for the successful salt separation. In this study, the solid-liquid separation was proposed prior to distillation of salt and a feasibility of the separation of the liquid salt by a metallic wire mesh (sieve) was tested for the reduction of the burden of the following vacuum distillation process

  16. Multi-column bioleaching of a uranium ore

    International Nuclear Information System (INIS)

    Meng Yunsheng; Zheng Ying; Liu Hui; Cheng Hao

    2014-01-01

    The technology of bioleaching uranium ore can increase the uranium leaching rate and shorten the leaching uranium period, save consumption of acid and oxidant, lower production costs. An experiment on multi-column bioleaching of a uranium ore was done using mesophilic bacteria, the average uranium recovery of 90% was achieved in 39 days. Compared with traditional process, leaching period was shortened to 39 d from 59 d, acid consumption and liquid-solid ratio were also reduced. The results showed it is suitable to bioleach the uranium ore. (authors)

  17. Surface decontamination in the old storage shed number 99 of the General Plan of IPEN/CNEN-SP, containing production equipment of natural uranium hexafluoride (UF{sub 6}), aiming at its decommissioning; Descontaminacao de superficies no antigo galpao de estocagem numero 99 da planta geral do IPEN/CNEN-SP, contendo equipamentos da producao de hexafluoreto de uranio natural, (UF{sub 6}), visando seu descomissionamento

    Energy Technology Data Exchange (ETDEWEB)

    Almeida, Claudio C. de; Cambises, Paulo B.S.; Paiva, Julio E. de; Paiva, Julio E. de; Silva, Teresina M.; Rodrigues, Demerval L., E-mail: calmeida@ipen.br, E-mail: cambises@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil)

    2013-11-01

    This paper presents the steps adopted in the operation planned for the decontamination of surfaces in the old storage shed number 99 the general layout of the Energy Research and Nuclear IPEN-CNEN/SP, Brazil, and contained various types of equipment originating from production hexafluoride natural uranium (UF6). This operation involved the planning, training of operators of the facility, analysis of workplaces and radiometric surveys for monitoring of external radiation and surface contamination. The training involved the procedures for decontamination of surfaces, segregation of materials and practical procedures for individual monitoring of contamination outside of the body. Were also established rules for the transport of radioactive materials in the internal and external facility and release of material and sites already decontaminated.

  18. Contribution to the Chemical and Technological Study of Ammonium Diuranate Precipitation

    International Nuclear Information System (INIS)

    Vuillemey, R.

    1962-01-01

    The present work is designed to study the relationship between the conditions for precipitation by ammonia and the properties of ammonium diuranate obtained either from uranyl nitrate solution or from gaseous uranium hexafluoride. In each case the optimum processes are defined leading on the one hand to uranate which can afterwards be treated in a reduction- fluorination oven to give uranium tetrafluoride, and on the other hand to a uranate suitable for the production of a sinterable uranium oxide. In particular it is shown that the treatment of uranyl nitrate solutions by stoichiometric quantities of ammonia leads to the complete precipitation of the uranium leaving less than 1 mg/litre of uranium in the solution, whereas the treatment of uranium hexafluoride necessitates the use of at least 8 times the stoichiometric quantity. (author) [fr

  19. Demand forecast for rail shipment of radioactive material in the United States

    International Nuclear Information System (INIS)

    Allen, G.C.; Cashwell, J.W.

    1981-01-01

    A summary of the market potential for radioactive material (in millions of ton-miles) is presented in tabular form. These include the following: milled uranium ore; mill tailings; natural uranium hexafluoride; enriched uranium hexafluoride; fresh fuel, spent fuel; low-level waste; transuranic waste; and high-level waste. The maximum realistic market share for rail carriers is always less than these values because of the lack of rail access to some shipping and receiving facilities, small material quantities which could most easily move by other modes, short shipping distances for certain transport segments and greater operational convenience of other modes for some material categories. While market share and revenues for radioactive material are presently small, rail carriers appear to have a market advantage for milled uranium ore, transuranic waste and high-level waste. The potential for a significantly increased market share exists for spent fuel and uranium hexafluoride. While more fresh fuel and low-level waste can be transported by rail, it is unlikely that rail market share for radioactive materials (RAM) in general will rise to the potential maximum because many of these materials have historically been moved by truck and transported in frequent, small shipments

  20. Chemistry of the 5g Elements: Relativistic Calculations on Hexafluorides.

    Science.gov (United States)

    Dognon, Jean-Pierre; Pyykkö, Pekka

    2017-08-14

    A Periodic System was proposed for the elements 1-172 by Pyykkö on the basis of atomic and ionic calculations. In it, the elements 121-138 were nominally assigned to a 5g row. We now perform molecular, relativistic four-component DFT calculations and find that the hexafluorides of the elements 125-129 indeed enjoy occupied 5g states. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  1. Chemistry of the 5g elements. Relativistic calculations on hexafluorides

    International Nuclear Information System (INIS)

    Dognon, Jean-Pierre; Pyykkoe, Pekka

    2017-01-01

    A Periodic System was proposed for the elements 1-172 by Pyykkoe on the basis of atomic and ionic calculations. In it, the elements 121-138 were nominally assigned to a 5g row. We now perform molecular, relativistic four-component DFT calculations and find that the hexafluorides of the elements 125-129 indeed enjoy occupied 5g states. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  2. Chemistry of the 5g elements. Relativistic calculations on hexafluorides

    Energy Technology Data Exchange (ETDEWEB)

    Dognon, Jean-Pierre [NIMBE, CEA, CNRS, Universite Paris-Saclay, CEA Saclay, Gif-sur-Yvette (France); Pyykkoe, Pekka [Department of Chemistry, University of Helsinki (Finland)

    2017-08-14

    A Periodic System was proposed for the elements 1-172 by Pyykkoe on the basis of atomic and ionic calculations. In it, the elements 121-138 were nominally assigned to a 5g row. We now perform molecular, relativistic four-component DFT calculations and find that the hexafluorides of the elements 125-129 indeed enjoy occupied 5g states. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  3. Determination of boron in uranium and aluminium by high pressure liquid chromatography (HPLC)

    International Nuclear Information System (INIS)

    Rao, Radhika M.; Aggarwal, S.K.

    2003-01-01

    Experiments were conducted for the determination of boron in U 3 O 8 powder and aluminium metal using dynamically modified reversed phase high pressure liquid chromatography (RP-HPLC) and using precolumn chromogenic agent viz. curcumin for complexing boron. The complex was separated from the excess of reagent and determined by HPLC. The boron curcumin complex (rosocyanin) was formed after extraction of boron with 2-ethyl-1,3-hexane diol (EHD). Linear calibration curves for boron amounts in the range of 0.02 μg to 0.5 μg were developed and used for the determination of boron in aluminium and uranium samples. (author)

  4. The handling of plutonium hexafluoride (1962); Manipulation de l'hexafluorure de plutonium (1962)

    Energy Technology Data Exchange (ETDEWEB)

    Berard, Ph [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1961-11-15

    The major problem posed in this work is the instability of plutonium hexafluoride. The influence of various factors on the decomposition of the fluoride has been studied: physical aspect of the walls, nature of the metal and its pretreatment, influence of the temperature. A means of detecting plutonium-239 in a metallic apparatus by {gamma}-ray counting has been developed; the sensitivity is of the order of half a milligram, but the precision is very low (about 50 per cent). Yields of over 95 per cent have been obtained for the transfer of plutonium during the preparation and sublimation of the hexafluoride. This study confirms the possibility of using plutonium hexafluoride for the extraction of plutonium from irradiated fuel elements by a dry method. (author) [French] Le probleme majeur de cette etude a ete l'instabilite de l'hexafluorure de plutonium. Nous avons etudie l'influence de divers facteurs sur la decomposition de l'hexafluorure: aspect physique des parois, nature du metal et de son pretraitement, influence de la temperature. Nous avons mis au point un mode de detection du plutonium-239 dans un appareillage metallique par comptage du rayonnement {gamma}; la sensibilite est de l'ordre du demi-milligramme, mais la precision est tres faible (50 pour cent environ). Nous avons obtenu des rendements depassant 95 pour cent dans le transfert du plutonium au cours de la fabrication et de la sublimation de l'hexafluorure. Cette etude confirme la possibilite d'utiliser l'hexafluorure de plutonium dans l'extraction du plutonium des combustibles irradies par voie seche. (auteur)

  5. Iron liquid-argon and uranium liquid-argon calorimeters for hadron energy measurement

    CERN Document Server

    Fabjan, Christian Wolfgang; Lankford, A J; Rehak, P; Struczinski, W; Willis, W J

    1977-01-01

    The authors studied, with a specially designed hadron calorimeter, the contributions of different mechanisms affecting the energy resolution of such instruments. It is shown that in ordinary materials the resolution is dominated by 'nuclear fluctuations'. Measurements with a uranium calorimeter show that these fluctuations can be effectively compensated by the amplifying effect of nuclear fission in uranium. The resolution at low energies is good ( sigma =9.6% for 10 GeV/c pions) and improving with energy. (12 refs).

  6. Research and economic evaluation on uranium enrichment by gaseous diffusion process in Japan

    International Nuclear Information System (INIS)

    Aochi, T.; Takahashi, S.

    1977-01-01

    Research and development works on uranium enrichment by gaseous diffusion process were carried out by JAERI, IPCR and industries since 1965. There are two important keys to reduce the uranium separation cost. One is the characteristics of the barrier and the other is financing and/or political planning. The technics to prepare the barrier with pore diameter of 40A have been developed with polytetrafluoroethylene, alumina and nickel. The experiment on corrosion behavior of PTFE barriers has shown better characteristics than the others. In the field of engineering research, the adiabatic efficiency of axial compressor for UF 6 was resulted to as high as 90% by long term operation tests. Based on these experimental data, techno-economic evaluation on a uranium enrichment plant was carried out with regard to the optimization of separation efficiency, numbers of step and operating conditions of the plant. Sensitivity in the separation cost were calculated as a function of pore diameter, uranium hexafluoride cost, plant capacity, electric power cost, and the plant annual expenditure. A financing plan must be such as to achieve 1. maximization of debt in a percentage of total capitalization 2. off-take contracts to utilities as security for financing 3. minimization of risks to equity and achievable cost of capital. Therefore the cash flow analysis and the schedule for construction and operation are very important for a economical feasibility of a uranium enrichment plant. To minimize the risk, not only economical but also political environment are important. The governmental supports and international agreements will be necessary

  7. A review of the environmental impact of mining and milling of radioactive ores, upgrading processes, and fabrication of nuclear fuels

    International Nuclear Information System (INIS)

    Costello, J.M.; Davy, D.R.; Cattell, F.C.R.; Cook, J.E.

    1980-01-01

    The subject is discussed under the headings: uranium mining; milling of uranium ores; manufacture of uranium hexafluoride; uranium enrichment; fuel manufacture and fabrication; environmental impact (use of natural resources; effluents from fuel cycle operations; occupational health; public health); alternative fuel cycles; additional waste treatment. (U.K.)

  8. Active-interrogation measurements of fast neutrons from induced fission in low-enriched uranium

    International Nuclear Information System (INIS)

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

    2014-01-01

    A detection system was designed with MCNPX-PoliMi to measure induced-fission neutrons from U-235 and U-238 using active interrogation. Measurements were then performed with this system at the Joint Research Centre in Ispra, Italy on low-enriched uranium samples. Liquid scintillators measured induced fission neutrons to characterize the samples in terms of their uranium mass and enrichment. Results are presented to investigate and support the use of organic liquid scintillators with active interrogation techniques to characterize uranium containing materials. -- Highlights: • We studied low-enriched uranium using active-interrogation experiments including a deuterium–tritium neutron generator and an americium–lithium isotopic neutron source. • Liquid scintillators measured induced-fission neutrons from the active-interrogation methods. • Fast-neutron (DT) and thermal-neutron (Am–Li) interrogation resulted in the measurement of trends in uranium mass and 235 U enrichment respectively. • MCNPX-PoliMi, the Monte Carlo transport code, simulated the measured induced-fission neutron trends in the liquid scintillators

  9. Active-interrogation measurements of fast neutrons from induced fission in low-enriched uranium

    Energy Technology Data Exchange (ETDEWEB)

    Dolan, J.L., E-mail: jldolan@umich.edu [Department of Nuclear Engineering and Radiological Sciences, University of Michigan, Ann Arbor, MI 48109 (United States); Marcath, M.J.; Flaska, M.; Pozzi, S.A. [Department of Nuclear Engineering and Radiological Sciences, University of Michigan, Ann Arbor, MI 48109 (United States); Chichester, D.L. [Idaho National Laboratory, Idaho Falls, ID 83415 (United States); Tomanin, A.; Peerani, P. [European Commission, Joint Research Centre, Institute for Transuranium Elements, Ispra (Italy)

    2014-02-21

    A detection system was designed with MCNPX-PoliMi to measure induced-fission neutrons from U-235 and U-238 using active interrogation. Measurements were then performed with this system at the Joint Research Centre in Ispra, Italy on low-enriched uranium samples. Liquid scintillators measured induced fission neutrons to characterize the samples in terms of their uranium mass and enrichment. Results are presented to investigate and support the use of organic liquid scintillators with active interrogation techniques to characterize uranium containing materials. -- Highlights: • We studied low-enriched uranium using active-interrogation experiments including a deuterium–tritium neutron generator and an americium–lithium isotopic neutron source. • Liquid scintillators measured induced-fission neutrons from the active-interrogation methods. • Fast-neutron (DT) and thermal-neutron (Am–Li) interrogation resulted in the measurement of trends in uranium mass and {sup 235}U enrichment respectively. • MCNPX-PoliMi, the Monte Carlo transport code, simulated the measured induced-fission neutron trends in the liquid scintillators.

  10. Treatment of liquid effluent from uranium mines and mills. Report of a co-ordinated research project 1996-2000

    International Nuclear Information System (INIS)

    2004-10-01

    Treatment and control of liquid effluents produced during uranium mining and milling operations is an integral part of environmental project management. Research has continued to add to the large body of science that has been built up around the treatment of radioactive and non-radioactive effluents to minimize their long-term environmental impact. The objective of the meetings on which this publication is based was to exchange information on active effluent treatment technologies that have application during operations and passive treatment techniques such as constructed wetlands and use of micro-organisms that are applicable during project reclamation and long-term care and maintenance. Papers describe effluent treatment case histories from active uranium mining and processing operations as well as effluent treatment research on both active and passive systems that have potential application under a wide range of operating and post-operational conditions including new information on high-density sludge from effluent neutralization (Australia), aerated manganese hydroxide for removal of radium (China), nanofiltration and macropore resins to treat mine water (Australia and China), in situ microbial treatment and permeable reactive walls for treatment of contaminated groundwater (Germany), construction of wetlands to treat mine water runoff (Australia and Germany), biogenic granules to remove 226 Ra from mill effluent (India), self-remediation of acidic in situ leach aquifers (Kazakhstan) and sorption characteristics of soil for self-remediation of contaminated groundwater (Hungary). These and other topics presented in this publication will be of interest to technical personnel who deal with day-to-day practical aspects of liquid effluent control and treatment at uranium production facilities worldwide

  11. Waste monitoring of the uranium ore processing activities in Romania

    International Nuclear Information System (INIS)

    Nica, L.

    2002-01-01

    The uranium ore processing activities at the Feldioara site produce a range of liquid and solid waste that are monitored. Liquids are treated through decantation, pH correction and uranium precipitation before their release into the environment. The solid waste is gathered into ore specific area and are covered regularly with clay materials. (author)

  12. Determination of uranium distribution in the evaporation of simulated Savannah River Site waste

    International Nuclear Information System (INIS)

    Barnes, M.J.; Chandler, G.T.

    1995-01-01

    The results of an experimental program addressing the distribution of uranium in saltcake and supernate for two Savannah River Site waste compositions are presented. Successive batch evaporations were performed on simulated H-Area Modified Purex low-heat and post-aluminum dissolution wastes spiked with depleted uranium. Waste compositions and physical data were obtained for supernate and saltcake samples. For the H-Area Modified Purex low-heat waste, the product saltcake contained 42% of the total uranium from the original evaporator feed solution. However, precipitated solids only accounted for 10% of the original uranium mass; the interstitial liquid within the saltcake matrix contained the remainder of the uranium. In the case of the simulated post-aluminum dissolution waste; the product saltcake contained 68% of the total uranium from the original evaporator feed solution. Precipitated solids accounted for 52% of the original uranium mass; again, the interstitial liquid within the saltcake matrix contained the remainder of the uranium. An understanding of the distribution of uranium between supernatant liquid, saltcake, and sludge is required to develop a material balance for waste processing operations. This information is necessary to address nuclear criticality safety concerns

  13. Study of the Treatment of the Liquid Radioactive Waste Nong Son Uranium Ore Processing

    International Nuclear Information System (INIS)

    Nguyen Ba Tien; Trinh Giang Huong; Luu Cao Nguyen; Harvey, L.K.; Tran Van Quy

    2011-01-01

    Liquid waste from Nong Son uranium ore processing is treated with concentrated acid, agglomerated, leached, run through ion exchange and then treated with H 2 O 2 to precipitate yellowcake. The liquid radioactive waste has a pH of 1.86 and a high content of radioactive elements, such as: [U] 143.898 ppm and [Th] = 7.967 ppm. In addition, this waste contains many polluted chemical elements with high content, such as arsenic, mercury, aluminum, iron, zinc, magnesium, manganese and nickel. The application of the general method as one stage precipitation or precipitation in coordination with BaCl 2 is not effective. These methods generated a large amount of sludge with poor settling characteristics. The volume of final treated waste was large. This paper introduces the investigation of the treatment of this liquid radioactive waste by the method of two stage of precipitation in association with polyaluminicloride (PAC) and polymer. The impact of factors: pH, neutralizing agents, quantity of PAC and polymer to effect precipitation and improve the settling characteristics during processing was studied. The results showed that the processing of liquid radioactive waste treatment through two stages: first stage at pH = 3 and the second stage at pH = 8.0 with limited PAC and polymer (A 101) resulted in significant reduced volume of the treated waste. The discharged liquid satisfied the requirement of the National Technical Regulation on Industrial Waste Water (QCVN 24:2009). (author)

  14. Treatment alternatives of liquid radioactive waste containing uranium in phosphoric acid

    International Nuclear Information System (INIS)

    Bustamante Escobedo, Mauricio

    2003-01-01

    The UGDR, receives annually 100 [l] of liquid radioactive waste containing, highly acid (pH=0) uranium in phosphoric acid from the Laboratory of Chemical Analysis. This waste must be chemically and radiologically decontaminated before it can be discharged in accordance with local environmental standards. Chemical precipitation and evaporation test were carried out to define the operating conditions for the radiological decontamination of this radioactive waste and to obtain a solid waste that can be conditioned in a cement matrix. The evaporation process generates excellent rates of volume reduction, over 80%, but generates a pulp that is hard handle when submitted to a drying process. Chemical precipitation generates good results for decontaminating these solutions and reducing volume (above 50%) to obtain a uranium free effluent. The treatment with calcium carbonate generated an effluent with a low concentration of polluting agents. A preliminary test was carried out condition these solids in a cement matrix, using ratios of 0.45 waste/cement and 2 of water/cement. The mix prepared with waste from the sodium hydroxide treatment had low mechanical resistance resulting from the saline incrustations. The waste from the calcium carbonate treatment was very porous due to the water evaporation from the highly exothermic reaction between the waste and the cement. The mix of the calcium carbonate generated waste and the cement matrix needs to be optimized, since it generates favorable conditions for adhering with the cement matrix (au)

  15. Primary metals extraction by liquid membranes

    International Nuclear Information System (INIS)

    Subramanian, K.N.

    1980-01-01

    The extraction of copper and uranium by liquid membranes is presented. The recovery of uranium from wet process phosphoric acid is described. The development of this process has progressed through three stages, firstly the chemistry of uranium extraction as it pertains to liquid membrane systems. This was followed by continuous extraction tests on fresh black acid and on aged acid. Results on a 1 litre/minute pilot plant demonstrated that the process could be operated with a minimum of feed pretreatment and about 90% of uranium could be extracted. The extraction of copper from copper leach liquors is also described. (U.K.)

  16. Determination of 232Th, 230Th and 228Th in liquid effluents from uranium mining

    International Nuclear Information System (INIS)

    Godoy, Jose Marcus de Oliveira

    1979-10-01

    A liquid scintillator αlpha spectrometer was built for the determination of Th- 228 , Th- 230 and Th- 232 in liquid effluents from Uranium mines and mills. The resolution of the αlpha spectrometer was found to be 200-300 KeV, when the scintillator was 8% T0P0, 0,77% scintimix-4 (91% PP0 and 9% Dimetil-P0P0P) and 10% of naphthalene in toluene. Aliquat-336 in xylene (30% v/v) was used to separate the thorium isotopes from other interfering radionuclides (U- 238 , U- 234 , Ra- 226 , Po- 210 ). Under the extraction experimental conditions, the detection limits were 1,2 pCi/1 for Th- 232 , 1,2 pCi/1 for Th- 230 and 0,9 pCi/1 for Th- 228 , for 1000 minutes of counting time. (author)

  17. Evaluation of sulfur hexafluoride and helium for steam generator leak location: Final report

    International Nuclear Information System (INIS)

    Kassen, W.R.

    1987-01-01

    Since the use of sulfur hexafluoride as a tracer for identifying sources of primary to secondary leakage in PWR steam generators appeared to offer significant sensitivity advantages, the thermal stability of sulfur hexafluoride in water was evaluated at steam generator operating temperature. Significant decomposition was observed after 2 to 4 hours at temperature. Key decomposition products were fluoride and sulfide ions. Based on this observation and these limited test results, the use of SF 6 for PWR steam generator leak location can not be recommended at this time. A survey of 15 utilities was conducted in regard to their application experience with the helium tracer-mass spectroscopy technique for steam generator leak location. Although several successful steam generator integrity programs do not include use of this technique, it has proven to be a useful addition to the inspection program at some plants. No corrosion concerns appear to be associated with this technique

  18. Preconcentration of uranium in water samples using dispersive ...

    African Journals Online (AJOL)

    Preconcentration of uranium in water samples using dispersive liquid-liquid micro- extraction coupled with solid-phase extraction and determination with inductively coupled plasma-optical emission spectrometry.

  19. Isotope separation using vibrationally excited molecules

    International Nuclear Information System (INIS)

    1979-01-01

    This invention relates to isotope separation employing isotopically selective vibrational excitation and vibration-translation reactions of the excited particles. Uranium enrichment, using uranium hexafluoride, is a particular embodiment. (U.K.)

  20. Cristallini Material Review and Selection

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Nicholas [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Savina, Joseph [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division; Hebden, Andrew [Argonne National Lab. (ANL), Argonne, IL (United States). Nuclear Engineering Division

    2016-09-30

    The creation of a handheld unit to utilize the Cristallini method of uranium hexafluoride sampling requires the identification and qualification of suitable substrate materials. These materials will need to quickly and completely react with the process gas, resist vapor locking under vacuum, while being relatively inexpensive and homogeneous. Two forms of powdered alumina have been chosen for a head-to-head comparison during upcoming uranium hexafluoride tests. Both materials have shown ideal uptake characteristics during tungsten hexafluoride tests with a high loading capacity and no measureable breakthrough. They have also been shown to work well at vacuums below 10 Torr, are commercially available and inexpensive. In addition, two possible hydrogen fluoride trapping materials, sodium fluoride and saturated calcium carbonate, have been identified for further testing.

  1. Nuclear science and technology branch report 1975

    International Nuclear Information System (INIS)

    Hardy, C.J.

    1975-10-01

    Research programs are reported into topics such as the mining and treatment of uranium ore, the manufacture of uranium hexafluoride, enrichment of uranium, fuel manufacture, waste treatment, reprocessing, heavy water production and the uranium fuel cycle. The names of staff responsible for each project are indicated. (R.L.)

  2. Safety aspects of gas centrifuge enrichment plants

    International Nuclear Information System (INIS)

    Hansen, A.H.

    1987-01-01

    Uranium enrichment by gas centrifuge is a commercially proven, viable technology. Gas centrifuge enrichment plant operations pose hazards that are also found in other industries as well as unique hazards as a result of processing and handling uranium hexafluoride and the handling of enriched uranium. Hazards also found in other industries included those posed by the use of high-speed rotating equipment and equipment handling by use of heavy-duty cranes. Hazards from high-speed rotating equipment are associated with the operation of the gas centrifuges themselves and with the operation of the uranium hexafluoride compressors in the tail withdrawal system. These and related hazards are discussed. It is included that commercial gas centrifuge enrichment plants have been designed to operate safely

  3. Preparation of plutonium hexafluoride. Recovery of plutonium from waste dross (1962)

    International Nuclear Information System (INIS)

    Gendre, R.

    1962-01-01

    The object of this work is to study the influence of various physical factors on the rate of fluorination of solid plutonium tetrafluoride by fluorine. In a horizontal oven with a circulation for pure fluorine at atmospheric pressure and 520 deg. C, at a fluorine rate of 9 litres/hour, it is possible to transform 3 g of tetrafluoride to hexafluoride with about 100 per cent transformation and a recovery yield of over 90 per cent, in 4 to 5 hours. The fluorination rate is a function of the temperature, of the fluorine flow-rate, of the crucible surface, of the depth of the tetrafluoride layer and of the reaction time. It does not depend on the diffusion of the fluorine into the solid but is determined by the reaction at the gas-solid interface and obeys the kinetic law (1 - T T ) 1/3 = kt + 1. The existence of intermediate fluorides, in particular Pu 4 F 17 , is confirmed by a break in the Arrhenius plot at about 370 deg. C, by differences in the fluorination rates inside the tetrafluoride layer, and by reversible colour changes. The transformation to hexafluoride occurs with a purification with respect of the foreign elements present in the initial plutonium. Recovery of plutonium from waste dross: The study is based on the transformation of occluded plutonium particles to gaseous hexafluoride which is then decomposed thermally to the tetrafluoride which can be reintroduced directly in the production circuit. Under the conditions considered this process is not applicable industrially. After milling, it is possible to separate the dross into enriched (75 per cent Pu in 2.6 per cent by weight of dross) and depleted portions. By prolonged fluorination (16 hours) of the various fractions it is possible to recover about 80 per cent of the plutonium. A treatment plant using fluidization, as described at the end of this study, should make it possible to substantially improve the yield. (author) [fr

  4. Uranium hexaflouride freezer/sublimer process simulator/trainer

    International Nuclear Information System (INIS)

    Carnal, C.L.; Belcher, J.D.; Tapp, P.A.; Ruppel, F.R.; Wells, J.C.

    1991-01-01

    This paper describes a software and hardware simulation of a freezer/sublimer unit used in gaseous diffusion processing of uranium hexafluoride (UF 6 ). The objective of the project was to build a plant simulator that reads control signals and produces plant signals to mimic the behavior of an actual plant. The model is based on physical principles and process data. Advanced Continuous Simulation Language (ACSL) was used to develop the model. Once the simulation was validated with actual plant process data, the ACSL model was translated into Advanced Communication and Control Oriented Language (ACCOL). A Bristol Babcock Distributed Process Controller (DPC) Model 3330 was the hardware platform used to host the ACCOL model and process the real world signals. The DPC will be used as a surrogate plant to debug control system hardware/software and to train operators to use the new distributed control system without disturbing the process. 2 refs., 4 figs

  5. Application of alkaline leaching to the extraction of uranium from shale of the Vosges; Application de la lixiviation alcaline a l'extraction de l'uranium du schiste des Vosges

    Energy Technology Data Exchange (ETDEWEB)

    Mouret, P; Pottier, P; Le Bris, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires; Soudan, P [Centre d' Etude de Lalumine, Compagnie Pechiney (France)

    1958-07-01

    Description of chemical treatment of Vosges shales to obtain uranium by alkaline leaching. Mineralogy aspects of ore, physical and chemical conditions of leaching, solid/liquid separation, uranium recovery by either ion exchange process or electrolytic precipitation. (author)Fren. [French] Description du traitement chimique des schistes des Vosges pour extraire l'uranium en milieu alcalin. L'aspect mineralogique, les conditions physiques et chimiques de la lixiviation, la separation solide/liquide et la recuperation de l'uranium soit par echangeurs d'ions, soit par precipitation electrolytique y sont exposes. (auteur)

  6. Uranium enrichment in South Africa: from the world-unique Z-plant to the use of high-technology lasers

    International Nuclear Information System (INIS)

    McDowell, M.W.

    1995-01-01

    A historical discussion of the technology used in South Africa for the enrichment of uranium, as well as other technological spin-offs for the country that followed from the construction of the Z-plant. The national energy strategy and objectives of the government during the Apartheid years resulted in the development of several large-scale energy projects. The pressure of sanctions forced the Z-plant to be rushed into operation at an uneconomical capacity of 250 000 SWU per annum. In 1994 this implied that enriched uranium was produced at a cost of $200 per SWU while the world market price was below $90. While the production of enriched uranium at the Z-plant ceased early in 1995, the expertise gained will not be lost entirely. As a result of the high energy and financial capital intensive current methods of producing enriched uranium, research started in the early 1970's into alternative production processes making use of lasers. South Africa has opted for the MLIS (molecular laser isotope separation) process, as a result of its vast experience gained from the Z-plant in the handling of the molecular input gas UF6 (uranium hexafluoride), and this has been under development since the early 1980's. During 1994 significant progress was made with MLIS, in particular with single-step enrichment from natural uranium to better than 4% uranium 235 on a macro scale. The Atomic Energy Corporation of South Africa's strategy is to licence the process internationally. 3 tabs., 3 figs

  7. Study for uranium advantage as byproduct of the phosphorite from Brazilian Northeast

    International Nuclear Information System (INIS)

    Almeida, M.G. de.

    1974-01-01

    The distribution and recovery of uranium contained in marine phosphates from Northeast Brazil were investigated by treating these ores with hydrochloric acid. The average content of uranium in the phosphorite was found to be about 0.03%. The leaching of phosphate from the ore and the amount of solubilized uranium supplied the basic information for the uranium recovery. The solutions, obtained in laboratory, leaching the phosphorite with hydrochloric acid contained 40.70 mg:U/l. An analytical method to control the uranium solubilization was outlined. A liquid-liquid extraction of uranium from these leaching solutions was performed using mixture of 3.3% di-(2-ethyl-hexyl)-phosphoric acid and 2.2% TBP in kerosene. After extraction the phosphoric acid free from uranium is sent to the calcium hydrogeno-phosphate production. The uranium is stripped from the organic phase by alkaline treatment and then precipitated as diuranate. (Author) [pt

  8. An automated, self-verifying system for monitoring uranium in effluent streams

    International Nuclear Information System (INIS)

    Reda, R.J.; Pickett, J.L.

    1992-01-01

    In nuclear facilities such as nuclear fuel fabrication plants, a constant vigil is required to ensure that the concentrations of uranium in process or waste streams do not exceed required specifications. The specifications may be dictated by the process owner, a regulatory agency such as the US Nuclear Regulatory Agency or Environmental Protection Agency, or by criticality safety engineering criteria. Traditionally, uranium monitoring in effluent streams has been accomplished by taking periodic samples of the liquid stream and determining the concentration by chemical analysis. Despite its accuracy, chemical sampling is not timely enough for practical use in continuously flowing systems because of the possibility that a significant quantity of uranium may be discharged between sampling intervals. To completely satisfy regulatory standards, the liquid waste stream must be monitored for uranium on a 100% basis. To this end, an automated, radioisotopic liquid-waste monitoring system was developed by GE Nuclear Energy as an integral part of the uranium conversion and waste recovery operations. The system utilizes passive gamma-ray spectroscopy and is thus a robust, on-line, and nondestructive assay for uranium. The system provides uranium concentration data for process monitoring and assures regulatory compliance for criticality safety. A summary of the principles of system operation, calibration, and verification is presented in this paper

  9. The nuclear fuel cycle: (2) fuel element manufacture

    International Nuclear Information System (INIS)

    Doran, J.

    1976-01-01

    Large-scale production of nuclear fuel in the United Kingdom is carried out at Springfields Works of British Nuclear Fuels Ltd., a company formed from the United Kingdom Atomic Energy Authority in 1971. The paper describes in some detail the Springfields Works processes for the conversion of uranium ore concentrate to uranium tetrafluoride, then conversion of the tetrafluoride to either uranium metal for cladding in Magnox to form fuel for the British Mk I gas-cooled reactors, or to uranium hexafluoride for enrichment of the fissile 235 U isotope content at the Capenhurst Works of BNFL. Details are given of the reconversion at Springfields Works of this enriched uranium hexafluoride to uranium dioxide, which is pelleted and then clad in either stainless steel or zircaloy containers to form the fuel assemblies for the British Mk II AGR or advanced gas-cooled reactors or for the water reactor fuels. (author)

  10. Radioactively induced noise in gas-sampling uranium calorimeters

    International Nuclear Information System (INIS)

    Gordon, H.A.; Rehak, P.

    1982-01-01

    The signal induced by radioactivity of a U 238 absorber in a cell of a gas-sampling uranium calorimeter was studied. By means of Campbell's theorem, the levels of the radioactively induced noise in uranium gas-sampling calorimeters was calculated. It was shown that in order to obtain similar radioactive noise performance as U-liquid argon or U-scintillator combinations, the α-particles from the uranium must be stopped before entering the sensing volume of gas-uranium calorimeters

  11. Recovery of uranium as a by product of phosphorites from Brazilian northeast area

    International Nuclear Information System (INIS)

    Gonzaga, M.; Abrao, A.

    1976-01-01

    The extraction and recobery of uranium contained in marine phosphates of northeast Brazil were investigated by treating ores with hydrochloric acid. The average content of uranium in the ore was found to be about 0,03 percent which corresponds to the highest worldly known content of uranium in phoshorite. The solutions obtained in laboratory, by leaching the phosphorite with hydrochloric acid, contained 40-70mg U/1. A method to control the uranium solubilization was outlined. A liquid-liquid extrction of uranium from these liquors was performed using a mixture of 3 percent di (2-ethyl hexyl)-phosphoric acid and 2.2 percent TBP in Kerosene. An overall uranium recovery of about 85 percent was reached

  12. Observation of inner surface of flame-tower type reactor for uranium conversion

    International Nuclear Information System (INIS)

    Amamoto, Ippei; Terai, Takayuki; Umetsu, Hiroshi

    2003-01-01

    A fluorination reactor, which has been used to convert uranium tetrafluoride (UF 4 ) into uranium hexafluoride (UF 6 ), was completed after approximately 6000 hours operation at the uranium conversion facility in Japan. The observation of its inner surface was carried out to understand its corrosive condition and mechanism. The main wall of the reactor is made of Monel Alloy and its operational temperature is approximately 450degC at external surface under gaseous fluorine atmosphere. A sampling was undertaken from the most corrosive part of the reactor wall, and its analysis was carried out to obtain the data for the condition of appearance, thickness, macro and micro structure, etc. The results of observation are as follows: (1) The thickness decreased evenly (average 3.9 mm/year); (2) The chemical composition of corrosive products as coating was mainly nickel fluoride (NiF 2 ), which suggested that the corrosion mechanism could have been caused by the high temperature gas corrosion; (3) The total amount of coating was lower than that of a loss in thickness. For some reason, some of coating would seem to become extinct on the surface of the wall. The deterioration of coating, which formed a protector on the wall due to excess heating of the wall, the sand erosion effect by UF 4 , etc. have contributed to this state of condition. (author)

  13. Design, construction, commissioning and long term operational experience with the D0 Uranium/Liquid Argon calorimeter

    OpenAIRE

    Schamberger, Dean

    2014-01-01

    The D0 experiment was designed in the mid 1980s and ran at the Fermilab pp collider from 1992 through 2011. I describe the uranium-liquid argon calorimeter and its readout electronic which was upgraded in the late 1990s to handle the higher luminosity of the upgraded Tevatron during its second running period from 2001-2011. I summarize maintaining the calorimeter for 20 years of data taking. I further describe a few issues that arose during that time, including different types of noise and th...

  14. Irans Nuclear Program: Tehrans Compliance with International Obligations

    Science.gov (United States)

    2016-04-07

    reactors. Iran also has a uranium conversion facility, which converts uranium oxide into several compounds, including uranium hexafluoride. Tehran claims... uranium .  The importation of natural uranium metal and its subsequent transfer for use in laser enrichment experiments, including the production of...investigation of its nuclear activities, suspend its uranium enrichment program, suspend its construction of a heavy-water reactor and related

  15. 1996 year-end market review

    International Nuclear Information System (INIS)

    Anon.

    1996-01-01

    A summary of financial data for uranium markets in 1996 is provided. Spot market activity and buyers and sellers of spot uranium are outlined for the restricted and unrestricted market. Data on the concentrates, uranium hexafluoride, enriched uranium product, and term uranium markets are also presented. Market data is also provided for conversion and enrichment services

  16. Use of Savannah River Site facilities for blend down of highly enriched uranium

    International Nuclear Information System (INIS)

    Bickford, W.E.; McKibben, J.M.

    1994-02-01

    Westinghouse Savannah River Company was asked to assess the use of existing Savannah River Site (SRS) facilities for the conversion of highly enriched uranium (HEU) to low enriched uranium (LEU). The purpose was to eliminate the weapons potential for such material. Blending HEU with existing supplies of depleted uranium (DU) would produce material with less than 5% U-235 content for use in commercial nuclear reactors. The request indicated that as much as 500 to 1,000 MT of HEU would be available for conversion over a 20-year period. Existing facilities at the SRS are capable of producing LEU in the form of uranium trioxide (UO 3 ) powder, uranyl nitrate [UO 2 (NO 3 ) 2 ] solution, or metal. Additional processing, and additional facilities, would be required to convert the LEU to uranium dioxide (UO 2 ) or uranium hexafluoride (UF 3 ), the normal inputs for commercial fuel fabrication. This study's scope does not include the cost for new conversion facilities. However, the low estimated cost per kilogram of blending HEU to LEU in SRS facilities indicates that even with fees for any additional conversion to UO 2 or UF 6 , blend-down would still provide a product significantly below the spot market price for LEU from traditional enrichment services. The body of the report develops a number of possible facility/process combinations for SRS. The primary conclusion of this study is that SRS has facilities available that are capable of satisfying the goals of a national program to blend HEU to below 5% U-235. This preliminary assessment concludes that several facility/process options appear cost-effective. Finally, SRS is a secure DOE site with all requisite security and safeguard programs, personnel skills, nuclear criticality safety controls, accountability programs, and supporting infrastructure to handle large quantities of special nuclear materials (SNM)

  17. Uranium oxide recovering method

    International Nuclear Information System (INIS)

    Ota, Kazuaki; Takazawa, Hiroshi; Teramae, Naoki; Onoue, Takeshi.

    1997-01-01

    Nitrates containing uranium nitrate are charged in a molten salt electrolytic vessel, and a heat treatment is applied to prepare molten salts. An anode and a cathode each made of a graphite rod are disposed in the molten salts. AC voltage is applied between the anode and the cathode to conduct electrolysis of the molten salts. Uranium oxides are deposited as a recovered product of uranium, on the surface of the anode. The nitrates containing uranium nitrate are preferably a mixture of one or more nitrates selected from sodium nitrate, potassium nitrate, calcium nitrate and magnesium nitrate with uranium nitrate. The nitrates may be liquid wastes of nitrates. The temperature for the electrolysis of the molten salts is preferably from 150 to 300degC. The voltage for the electrolysis of the molten salts is preferably an AC voltage of from 2 to 6V, more preferably from 4 to 6V. (I.N.)

  18. Liquid-liquid extraction of uranium(VI) with cryptand-222 and Eosin as the counter ion

    International Nuclear Information System (INIS)

    Viji Jacob Mathew; Khopkar, S.M.

    1995-01-01

    Uranium(VI), (5 μg) was quantitatively extracted at pH 6.0 with 0.01M cryptand-222 in chloroform in the presence of 0.005M Eosin as the counter ion. The metal from the organic phase was stripped with 0.1M perchloric acid. Uranium(VI) from the aqueous phase was determined spectrophotometrically at 430 nm as its complex with oxine. The extraction was quantitative between pH 5.5-6.5. Nitrobenzene, chloroform and dichloromethane were the best diluents. The optimum extractant concentration was 0.01M, while that of Eosin was 0.005M. Except for perchloric acid (0.01M), other acids could not strip uranium. Uranium was separated from manganese, cadmium, lead, thallium and nickel, etc., in the multicomponent mixtures. The relative standard deviation was ±1%. (author). 18 refs., 1 fig., 6 tabs

  19. Contribution to the study of interactions between uranium hexafluoride and alkali fluorides

    International Nuclear Information System (INIS)

    Paillet, Alain

    1972-01-01

    The author describes the complexation of UF 6 with alkaline fluorides by various ways: a preliminary chemical study of the synthesis, a spectrographic study (diffraction of X-rays, Raman-laser spectroscopy, I.R. spectroscopy), a calorimetric study, at last a study of kinetics by thermogravimetry. The complexes present the formula MF, UF 6 or 2MF, UF 6 whatever is M (including Rb and Cs). The X ray diffraction study, made for analytical purposes, enabled to describe the spectra of NaUF 7 , Na 2 UF 8 , KUF 7 , RbUF 7 , CsUF 7 . For KUF 7 , RbUF 7 , CsUF 7 the tri-periodic array of the uranium atoms is cubic. The thermodynamical study shows that the initial stage of germination evolves, at room temperature, 40 or CO Kcal/mole for a reaction rate, lower than 5%, for all the complexes; then, approximately 16 Kcal/mole. For the ulterior stages, the activation energy for the inter-crystalline diffusion is about 6 Kcal/mole. Various types of original apparatus, working in fluorinating atmosphere, are described: particularly a miniaturized microcalorimeter, especially designed to gain a great sensitivity. (author) [fr

  20. Research on and economic evaluation of uranium enrichment by gaseous diffusion in Japan

    International Nuclear Information System (INIS)

    Aochi, T.; Takahashi, S.

    1977-01-01

    Research and development on uranium enrichment by the gaseous diffusion process have been carried out by the Japan Atomic Energy Research Institute, the Institute of Physical and Chemical Research, and industries since 1965. The paper describes the two important keys to reducing the cost of uranium separation. One is the characteristics of barriers and the other is financing and/or political planning. The techniques of preparing a barrier with pore diameter 40A have been developed with polytetrafluoroethylene (PTFE), alumina and nickel. Experiments on corrosion behaviour have indicated that PTFE barriers are the most favourable. In the field of engineering research, the adiabatic efficiency of the axial compressor for UF 6 was raised to as high as 90% by long-term operation tests. Based on these experimental data, technico-economic evaluation of a uranium enrichment plant was carried out for optimization of separation efficiency, number of steps and plant operating conditions. Sensitivity in the separation cost was calculated as a function of pore diameter, cost of uranium hexafluoride, plant capacity, cost of electric power, and annual expenditure of the plant. A finance plan must be such as to achieve: (a) maximization of debt in a percentage of total capital; (b) off-take contracts to utilities as security for financing; (c) minimization of risks to equity and achievable cost of capital. Therefore, the cash flow analysis and the schedule for construction and operation are very important for the economic feasibility of a uranium enrichment plant. To minimize the risk, the economic as well as the political environment is important. Government support and international agreements are necessary. (author)

  1. Study on technology for radioactive waste treatment and management from uranium production

    International Nuclear Information System (INIS)

    Vu Hung Trieu; Vu Thanh Quang; Nguyen Duc Thanh; Trinh Giang Huong; Tran Van Hoa; Hoang Minh Chau; Ngo Van Tuyen; Nguyen Hoang Lan; Vuong Huu Anh

    2007-01-01

    There is some solid and liquid radioactive waste created during producing Uranium that needs being treated and managed to keep our environment safe. This radioactive waste contains Uranium (U-238), Thorium (Th-232), Radium (Ra-226) and some heavy metals and mainly is low radioactive waste. Our project has researched and built up appropriate technology for treating and managing the radioactive waste. After researching and experimenting, we have built up four technology processes as follows: Technology for separating Radium from liquid waste; Technology for treating and managing solid waste containing Ra; Technology for separating Thorium from liquid waste after recovering radium; Technology for stabilizing solid waste from Uranium production. (author)

  2. Fuel-cycle facilities: preliminary safety and environmental information document. Volume VII

    Energy Technology Data Exchange (ETDEWEB)

    1980-01-01

    Information is presented concerning the mining and milling of uranium and thorium; uranium hexafluoride conversion; enrichment; fuel fabrication; reprocessing; storage options; waste disposal options; transportation; heavy-water-production facilities; and international fuel service centers.

  3. Fuel-cycle facilities: preliminary safety and environmental information document. Volume VII

    International Nuclear Information System (INIS)

    1980-01-01

    Information is presented concerning the mining and milling of uranium and thorium; uranium hexafluoride conversion; enrichment; fuel fabrication; reprocessing; storage options; waste disposal options; transportation; heavy-water-production facilities; and international fuel service centers

  4. Measurement of the enrichment of uranium-hexafluoride gas in product pipes in the centrifuge enrichment plant at Almelo

    International Nuclear Information System (INIS)

    Packer, T.W.; Lees, E.W.; Aaldijk, J.K.; Harry, R.J.S.

    1987-09-01

    One of the objectives of safeguarding centrifuge enrichment plants is to apply non-destructive measurements inside the cascade area to confirm that the enrichment level is in the low enriched uranium range. Research in the UK and USA has developed a NDA instrument which can confirm the presence of low enriched uranium on a rapid go/no go basis in cascade header pipework of their centrifuge enrichment plants. The instrument is based on a gamma spectroscopic measurement coupled with an X-ray fluorescence analysis. This report gives the results of measurements carried out at Almelo by the UKAEA Harwell, ECN Petten and KFA Juelich to determine if these techniques could be employed at Almelo and Gronau. The energy dispersive X-ray fluorescence analysis has been applied to determine the total mass of uranium in the gas phase, and the deposit correction technique and the two geometry technique have been applied at Almelo to correct the measured gamma intensities for those emitted by the deposit. After an executive summary the report discusses the principles of the two correction methods. A short description of the equipment precedes the presentation of the results of the measurements and the discussion. After the conclusions the report contains two appendices which contain the derivation of the formulae for the deposit correction technique and a discussion of the systematic errors of this technique. 8 figs.; 11 refs.; 6 tables

  5. Development of windowless liquid lithium targets for fragmentation and fission of 400-kW uranium beams

    CERN Document Server

    Nolen, J A; Hassanein, A; Novick, V J; Plotkin, P; Specht, J R

    2003-01-01

    The driver linac of the proposed rare isotope accelerator facility is designed to deliver 2x10 sup 1 sup 3 uranium ions per second at 400 MeV/u on target for radionuclide production via the fission and fragmentation mechanisms. The ion optics of the large acceptance, high-resolution fragment separators that follow the production target require primary beam spot widths of 1 mm. To cope with the resulting high power densities, windowless liquid lithium targets are being developed. The present designs build on existing experience with liquid lithium and liquid sodium systems that have been used for fusion and fission applications. However, no completely windowless systems have been developed or tested to date. For the beam power indicated above (400 kW), the flow requirements are up to about 20 m/s and 10 l/s linear and volume flow rates, respectively. The required target thickness is 1-1.5 g/cm sup 2 (2-3 cm lithium thickness). At this time a prototype windowless system with a lithium thickness of 1-2 cm is und...

  6. The Study of Isolated Bacteria Application for Bioremediation Agent of Uranium Radionuclide in the Environment

    International Nuclear Information System (INIS)

    Yazid, Mochd

    2007-01-01

    Application of the isolated bacteria on the Low Level Uranium Waste as uranium bioremediation agent in the environment has been studied. The objective of this research is to study the possibility of isolated bacteria to be used on uranium remediation process. The isolation of uranium resistance bacteria was carried out on the selective medium SBS containing 10 mg/l uranium, incubated at 37°C until the growth was visible. Selection of binding uranium bacteria was carried out based on their ability to grow on liquid medium containing various concentration of uranium that shacked on 120 rpm speed. The isolated bacteria with the highest specific growth rate constant (μ) were selected for biochemical characterization and identification by matching profile method. The result of this research showed that three selected isolate bacteria were able to grow well on liquid SBS medium until 100 mg/l uranium concentration. The identification results showed that two of them were suspected belong to the genus Pseudomonas and one isolates belong to the genus of Bacillus. The uranium reduction studied was performed by growing up the isolated bacteria on the SBS liquid medium that containing 40 mg/l uranium. Bacterial growth were measured by weighted of bacterial biomass and uranium concentration were measured by spectrophotometer. The research result showed that the selected isolates bacteria may applicable for bioremediation agent because of their ability to grow well on liquid SBS medium and their ability on uranium concentration reduction. The efficiency of reduction by Pseudomonas in the isolated bacteria one were 78.51 % and in the isolated bacteria three were 91.47 % , and Bacillus in the isolate bacteria six were 52.73%. (author)

  7. Fluorinated compounds in the uranium conversion process: risk analysis and proposition of pictograms; Os compostos fluorados nos processos da conversao do uranio: analise de riscos e proposicao de pictogramas

    Energy Technology Data Exchange (ETDEWEB)

    Jeronimo, Adroaldo Clovis; Oliveira, Wagner dos Santos, E-mail: acejota18@yahoo.com.br, E-mail: oliveira@feq.unicamp.br [Universidade Estadual de Campinas (UNICAMP), SP (Brazil). Fac. de Engenharia Quimica; Aquino, Afonso Rodrigues de, E-mail: araquino@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2012-03-15

    In the process of uranium hexafluoride production there are risks that must be taken into account since the time of completing the project chemist, in its conceptual stage, until to the stage of detailed design and are associated with the handling of chemicals, especially fluoride hydrogen and fluorine. This paper aims to address issues related to the prevention of risks related to industrial safety and health and the environment, considering the different stages of the uranium conversion. Take into account the safety warnings of the plant and, accordingly, make the proposition of pictograms adequate to alert operators of care to be taken during the proposition of pictograms adequate to alert operators of care to be taken during the conduct of these chemical processes. (author)

  8. On the applicability of the critical safety function concept to a uranium hexafluoride conversion unit

    International Nuclear Information System (INIS)

    Santos, F.C.; Goncalves, J.S.; Melo, P.F. Frutuoso e; Medeiros, J.A.C.C.

    2013-01-01

    This paper presents a discussion on the applicability on the critical safety function (CSF) concept as a design criterion for the new UF 6 conversion plant of Industrias Nucleares do Brazil (INB). This discussion is in the context of accident management, under the safety function oriented management. Safety functions may be understood as those whose loss may lead to releases of radioactive material or highly toxic chemicals, having possible radiological and/or occupational consequences for workers, the public or the environment. They should be designed to prevent criticality and to ensure adequate process confinement, thus preventing radioactive material releases that might lead to internal or external exposure and highly toxic chemical releases and exposure. The main hazards is the potential release of chemicals, especially HF and UF 6 . A criticality hazard exists only if the conversion facility processes uranium with a 235 U concentration greater than 1% Industrial activities for UF 6 production include handling and processing explosive, toxic and lethal chemicals, such as HF, H 2 and elemental F 2 , besides intermediate compounds containing uranium. State trees and definition of logical arrangements to construct an annunciation system are the next development stages, resulting form the establishment of applicable CSFs as representative of the next development stages, resulting from the establishment of applicable CSFs as representative of the various systems that make up the conversion plant. Discussed also in the biggest challenge of the development of this innovation, that is, the uncertainties related to the impact of human factors (not subject to monitoring by sensors or process conventional instrumentation). (author)

  9. Contribution to the study of the intermediate fluorides of uranium; Contribution a l'etude des fluorures intermediaires d'uranium

    Energy Technology Data Exchange (ETDEWEB)

    Nguyen-Hoang, Nghi [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1961-10-15

    The reaction of gaseous uranium hexafluoride with solid uranium tetrafluoride has been studied between 20 and 300 deg. C. The intermediate fluorides resulting from this reaction were prepared and then identified by chemical analysis and Debye-Scherrer diagrams. Their magnetic susceptibility and action on various common solvents were determined. The kinetic study was carried out up to 45 deg. C at a constant gas pressure equal to 17,7 mm of mercury. The experimental results indicate that the reaction, limited by the diffusion process of ionic reactants, obeys the kinetic law: L (1 - C) = k{radical}t. The observed rate constant K and the diffusion coefficient D vary with the temperature according to the expressions: K min{sup -1/2} = - (1,88 {+-} 0,22) 10{sup 8} exp[-(14100 {+-} 1400 cal/mole)/(RT)]; D cm{sup 2} sec{sup -1} = (1,15 {+-} 0,51) 10{sup 6} exp[-(30200 {+-} 5700 cal/mole)/(RT)]. (author) [French] La reaction de l'hexafluorure d'uranium gazeux sur le tetrafluorure d'uranium solide a ete etudiee entre 20 et 300 deg. C. Les fluorures intermediaires resultant de cette reaction ont ete prepares, puis identifies par analyses chimiques et par diagrammes Debye-Scherrer. Leur susceptibilite magnetique et leur action sur divers solvants usuels ont ete determinees. L'etude cinetique a ete entreprise jusqu'a 45 deg. C, sous une pression de gaz constante et egale a 17,7 mm de mercure. Les resultats experimentaux obtenus indiquent que la reaction, limitee par le processus de diffusion de reactifs ioniques, suit la loi cinetique: L (1 - C) = k{radical}t. La constante de vitesse observee K et le coefficient de diffusion D varient avec la temperature selon les expressions: K min{sup -1/2} = - (1,88 {+-} 0,22) 10{sup 8} exp[-(14100 {+-} 1400 cal/mole)/(RT)]; D cm{sup 2} sec{sup -1} = (1,15 {+-} 0,51) 10{sup 6} exp[-(30200 {+-} 5700 cal/mole)/(RT)]. (auteur)

  10. The mechanism of uranium adsorption on Resin 508 and isoelectric point of the resin

    International Nuclear Information System (INIS)

    Han Qingping; Lu Weichang; Su Huijuan; Hu Jinbo; Zhang Liqin; Chen Banglin

    1990-01-01

    The adsorption process of uranium by Resin 508 at the solid-liquid interface was investigated and the mechanism of uranium adsorption including adsorption dynamics, adsorption thermodynamics and isoelectric point of resin was studied. The results are as follows: The maximum of uranium adsorption is attained at pH5-7; Uranium adsorption isotherm by Resin 508 in experimental conditions agrees with Langmuir's adsorption isotherm, the maximum of uranium adsorbed (Vm) is 716 mg U/g-dried resin; The adsorption of uranium by Resin 508 is an endothermic reaction and ΔH = 16.87 kJ/mol; The exchange-adsorption rate is mainly controlled by liquid film diffusion; The isoelectric points of Resin 508 before and after uranium adsorption are found to be pH7.5 and pH5.7 respectively. It is a specific adsorption for uranium

  11. The study of the possibilities for the processing and exploatation of nuclear raw materials

    International Nuclear Information System (INIS)

    Smalc, A.

    1977-01-01

    Laboratory scale fluorinations of uranium tetrafluoride with elemental fluorine under pressure and the reactions of uranium hexafluoride with boron trioxide and sulphur are described. A review of the reactions with UF 6 and the processes for the conversion of UF 6 into non-volatile uranium compounds is given

  12. Treatment of effluents from the nuclear fuel cycle reconversion stage

    International Nuclear Information System (INIS)

    Ladeira, Ana C.Q.; Morais, Carlos A.; Goncalves, Joao S.; Souza, Pedro de

    2007-01-01

    The conversion of uranium hexafluoride (UF 6 ) into uranium dioxide (UO 2 ) takes place in Resende (RJ) at the Nuclear Fuel Factory - FCN. The process generates liquid effluents with significant concentrations of uranium which might be treated before being discharged into the environment. This work is aimed at the recovery of uranium from two distinct liquid effluents; one with high carbonate content and the other with elevated fluoride concentration. It is also presented a study about carbonate removal from an effluent that consists of water - methanol solution generated during the filtration step of the ammonium uranyl tricarbonate (AUT). The results showed that (1) the uranium from the carbonated solution can be recovered through the ion exchange technique using the strong base anionic resin IRA 910-U since carbonate has been removed as CO 2 after heating; (2) the most suitable technique to recover uranium from the fluoride solution is by precipitation as (NH 4 ) 2 UO 4 F 2 - ammonium fluorouranate peroxide (APOFU), (3) the solution free of carbonate can be added to the fluoride solution and the uranium from the final solution can be recovered by precipitation as ammonium fluorouranate peroxide as well; (4) the carbonate from the water-methanol solution can be recovered as calcium carbonate through the addition of calcium chloride or it can be removed through the addition of sulfuric acid. The product formed by adding sulfuric acid is ammonium sulfate and might be used as fertilizer. (author)

  13. An isotope-enrichment unit and a process for isotope separation

    International Nuclear Information System (INIS)

    1981-01-01

    A process and equipment for isotope enrichment using gas-centrifuge cascades are described. The method is described as applied to the separation of uranium isotopes, using natural-abundance uranium hexafluoride as the gaseous-mixture feedstock. (U.K.)

  14. On the applicability of the critical safety function concept to a uranium hexafluoride conversion unit

    Energy Technology Data Exchange (ETDEWEB)

    Santos, F.C.; Goncalves, J.S.; Melo, P.F. Frutuoso e; Medeiros, J.A.C.C., E-mail: fcruz@nuclear.ufrj.br, E-mail: jsgoncalves@inb.gov.br, E-mail: frutuoso@nuclear.ufrj.br, E-mail: canedo@imp.ufrj.br [Coordenacao dos Programas de Pos-Graduacao em Engenharia (COPPE/UFRJ), Rio de Janeiro, RJ (Brazil)

    2013-07-01

    This paper presents a discussion on the applicability on the critical safety function (CSF) concept as a design criterion for the new UF{sub 6} conversion plant of Industrias Nucleares do Brazil (INB). This discussion is in the context of accident management, under the safety function oriented management. Safety functions may be understood as those whose loss may lead to releases of radioactive material or highly toxic chemicals, having possible radiological and/or occupational consequences for workers, the public or the environment. They should be designed to prevent criticality and to ensure adequate process confinement, thus preventing radioactive material releases that might lead to internal or external exposure and highly toxic chemical releases and exposure. The main hazards is the potential release of chemicals, especially HF and UF{sub 6}. A criticality hazard exists only if the conversion facility processes uranium with a {sup 235}U concentration greater than 1% Industrial activities for UF{sub 6} production include handling and processing explosive, toxic and lethal chemicals, such as HF, H{sub 2} and elemental F{sub 2}, besides intermediate compounds containing uranium. State trees and definition of logical arrangements to construct an annunciation system are the next development stages, resulting form the establishment of applicable CSFs as representative of the next development stages, resulting from the establishment of applicable CSFs as representative of the various systems that make up the conversion plant. Discussed also in the biggest challenge of the development of this innovation, that is, the uncertainties related to the impact of human factors (not subject to monitoring by sensors or process conventional instrumentation). (author)

  15. Contacting gases and liquids

    International Nuclear Information System (INIS)

    Robinson, L.F.; Cahalan, M.J.

    1980-01-01

    A process is described for contacting substantially immiscible phases to transfer material from one phase to another, which comprises passing the phases through a contactor, while causing portions of at least one phase to be repeatedly passed through at least one other phase. One phase in the contactor is gaseous, and another liquid. A further phase can be liquid or solid The process may be used for extracting impurities from china clay, or extracting uranium values from ore with oxygen gas acting to oxidise the uranium. (author)

  16. Chemical aspects of nuclear fuel fabrication processes

    Energy Technology Data Exchange (ETDEWEB)

    Naylor, A; Ellis, J F; Watson, R H

    1986-04-01

    Processes used by British Nuclear Fuels plc for the conversion of uranium ore concentrates to uranium metal and uranium hexafluoride, are reviewed. Means of converting the latter compound, after enrichment, to sintered UO/sub 2/ fuel bodies are also described. An overview is given of the associated chemical engineering technology.

  17. Study on uranium adsorption ability of tannix resin from solution

    International Nuclear Information System (INIS)

    Le Thi Kim Dung; Le Quang Thai; Nguyen Lanh; Le Ngoc Thuy

    2004-01-01

    During past years, generated liquid waste from uranium ore processing has been treated by co-precipitation method in ITRRE. In this liquid waste treatment process, mixing liquid waste and lime, decantation, filtration of precipitate were implemented. The treated fluid has underlimited toxic concentration and ensures for moving into environment. Residue was dried and packed into drums as low level radioactive waste. Next to the advantages of this method such as simplest technology, cheapest cost, easy operation. Some amount of secondary radioactive waste as noncombustible materials must be stored with complicated technologies a highly cost. We have been researching a new liquid waste treatment system replaceable precipitation system. In the new process, insoluble tannin is utilized as adsorbent of uranium liquid waste. Advantage of insoluble tannin is expected to be possible to reduce its volume incineration as well as its adsorption ability. Those are the reasons why tannix resin is used this research subject. In this subject, we have studied adsorption capacity of uranium in Tannix, relation of adsorption rate and pH, the change of adsorption ability of column system, the pyrolysis curve of dried Tannix (author)

  18. URANIUM DECONTAMINATION WITH RESPECT TO ZIRCONIUM

    Science.gov (United States)

    Vogler, S.; Beederman, M.

    1961-05-01

    A process is given for separating uranium values from a nitric acid aqueous solution containing uranyl values, zirconium values and tetravalent plutonium values. The process comprises contacting said solution with a substantially water-immiscible liquid organic solvent containing alkyl phosphate, separating an organic extract phase containing the uranium, zirconium, and tetravalent plutonium values from an aqueous raffinate, contacting said organic extract phase with an aqueous solution 2M to 7M in nitric acid and also containing an oxalate ion-containing substance, and separating a uranium- containing organic raffinate from aqueous zirconium- and plutonium-containing extract phase.

  19. The action of uranium hexafluoride on some metallic fluorides (1962); Action de l'hexafluorure d'uranium sur quelques fluorures metalliques (1962)

    Energy Technology Data Exchange (ETDEWEB)

    Michallet, M [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1961-12-15

    A metallic difluoride is inert to UF{sub 6} unless the metal can exist in a higher valency state. In this case, UF{sub 6} acts as an oxidising agent and is transformed into UF{sub 4}. The fluorides of tri- and tetra-valent metals give rise to new compounds when they are maintained at a high temperature (500 deg. C) in the presence of uranium hexachloride vapour. The products obtained are characterized by their X-ray diffraction diagrams. The distributions of the lines of the powder diagrams are very similar to that of U{sub 4}F{sub 17}. Assuming that this resemblance is due to a stacking of identical fluorine atoms, it can be calculated that the corresponding structure is given by the theoretical formulae: MeF{sub 3}, 0,562 UF{sub 6}; MeF{sub 4}, 0,396 UF{sub 6} which are in good agreement with chemical measurements. (author) [French] Un di-fluorure metallique est inerte vis-a-vis de UF{sub 6}, sauf si le metal est susceptible d'exister a une valence plus elevee. Dans ce cas, UF{sub 6} joue le role d'un oxydant et se transforme en UF{sub 4}. Les fluorures de metaux tri et tetravalents donnent naissance a des composes nouveaux quand ils sont maintenus a haute temperature (500 deg. C) en presence de vapeur d'hexafluorure d'uranium. Les produits obtenus sont caracterises par leurs diagrammes de diffraction X. Les distributions de raies des diagrammes de poudre sont tres voisines de celles de U{sub 4}F{sub 17}. En supposant que cette analogie resulte d'un empilement d'ions fluor identique, le calcul conduit aux formules theoriques suivantes: MeF{sub 3}, 0,562 UF{sub 6}; MeF{sub 4}, 0,396 UF{sub 6} en bon accord avec les resultats des dosages chimiques. (auteur)

  20. Manufacture of uranium dioxide powder

    International Nuclear Information System (INIS)

    Becker, M.

    1976-01-01

    Uranium dioxide powder is prepared by the AUC (ammonium uranyl carbonate) method. Supplementing the known process steps, the AUC, after separation from the mother liquor, is washed with an ammonium hydrogen carbonate or an NH 4 OH solution and is subsequently post-treated with a liquid which reduces the surface tension of the residual water in an AUC. Such a liquid is, for instance, alcohol

  1. Spectrophotometric determination of uranium with arsenazo previous liquid-liquid extraction and colour development in organic medium

    International Nuclear Information System (INIS)

    Palomares Delgado, F.; Vera Palomino, J.; Petrement Eguiluz, J. C.

    1964-01-01

    The determination of uranium with arsenazo is hindered by a great number of cation which form stable complexes with the reactive and may given rise to serious interferences. By studying the optimum conditions of uranium the extraction be means of tributylphosphate solutions dissolved in methylisobuthylketone, under conditions for previous masking of the interfering cations, an organic extract was obtained containing all the uranium together with small amounts of iron. The possible interference derived from the latter element is avoided by reduction with hydroxylammoniumchlorid followed by complex formation of the Fe(II)-ortophenantroline compound in alcoholic medium. (Author) 17 refs

  2. Present status of refining and conversion facility dismantling. Progress in 2008 first half of the fiscal year

    International Nuclear Information System (INIS)

    Kado, Kazumi; Sugitsue, Noritake; Morimoto, Yasuyuki; Ikegami, Sohei; Takahashi, Nobuo; Tokuyasu, Takashi

    2009-06-01

    The Refining and Conversion Facility located in the Ningyo-toge Environmental Engineering Center. Process of natural uranium conversion facility (PNC Process) and reprocessed uranium conversion facility (two-stage dry fluorination system) is in a Refining and Conversion Facility. This building started construction in 1979 and was completed in October 1981. The PNC process operated from March 1982 to March 1991. As a result, uranium hexafluoride of about 385 tonU was manufactured. Also, the reprocessed uranium conversion process operated from December 1982 to July 1999. As a result, uranium hexafluoride of about 338 tonU was manufactured. The demonstration of the demolition method was done using the PNC process after the end of operation. The schedule which will finish dismantling of all equipment in a radiation controlled area is by the 2011 fiscal year. This report summarized the present situation by the first half of the 2008 fiscal year of a Refining and Conversion Facility decommissioning. (author)

  3. Radiation protection program applied to occupationally exposed individuals at the IPEN/CNEN-SP pilot plant in the 1980s for natural uranium compounds

    International Nuclear Information System (INIS)

    Silva, Teresinha de Moraes da; Sordi, Gian Maria A.A.; Vasques, Francisco Mário Feijó

    2017-01-01

    The work evidences the chemical processing of natural uranium from the yellowcake phase to the production of UF 6 natural uranium hexafluoride, a process carried out at the IPEN/CNEN-SP pilot plant. Radiation protection management was intended to monitor occupationally exposed individuals - IOEs, the workplace and the environment. An individual monitoring program for IOEs was developed for both external irradiation and incorporation of radioactive material. The IOEs were monitored externally with film-type dosimeters and the in vitro method was applied internally for urine analysis. For the workplace the monitoring program for equipment and floors was developed, determining the exposure rate from the process equipment, surface contamination expressed in Bq.cm -2 in equipment and floors, complemented by the air monitoring program both for the worker as well as for the workplace. Cellulose filters with aerodynamic diameter of 0.3 micron to 8.0 micron were used

  4. Distribution of uranium in marine sediments

    International Nuclear Information System (INIS)

    Ordonez R, E.; Ramirez T, J.J.; Lopez M, J.; Aspiazu, J.; Ruiz F, A.C.; Valero C, N.

    2008-01-01

    The marine sediments obtained by means of a sampling nucleus in the Gulf of Tehuantepec, Mexico, they have been object of crystallographic and morphological characterization. The PIXE analysis of some samples in study is shown. The normal methodology to carry out the alpha spectroscopy indicates that the sample should be dissolved, but due to the nature of the marine sediments, it thinks about the necessity to make a fractional separation of the sample components. In each stratum of the profile it separates the organic part and the mineral to recover the uranium. It was observed that in the organic phase, the uranium is in two oxidation states (IV and Vl), being necessary the radiochemical separation with a liquid/liquid column chromatographic that uses the di-2-ethyl hexyl phosphoric acid as stationary phase. The uranium compounds extracts are electrodeposited in fine layers on stainless steel disks to carry out the analysis by alpha spectroscopy. The spectroscopic analysis of the uranium indicates us that for each stratum one has a difference marked in the quotient of activities of 234 U/ 238 U that depends on the nature of the studied fraction. These results give us a clear idea about how it is presented the effect of the uranium migration and other radioelements in the biosphere, with what we can determine which are the conditions in that these have their maximum mobility and to know their diffusion patterns in the different media studied. (Author)

  5. Methodology of simultaneous analysis of Uranium and Thorium by nuclear and atomic techniques. Application to the Uranium and Thorium dosing in mineralogic samples

    International Nuclear Information System (INIS)

    Fakhi, S.

    1988-01-01

    This work concerns essentially the potential applications of 100 kW nuclear reactor of Strasbourg Nuclear Research Centre to neutron activation analysis of Uranium and Thorium. The Uranium dosing has been made using: 239-U, 239-Np, fission products or delayed neutrons. Thorium has been showed up by means of 233-Th or 233-Pa. The 239-U and 233-Th detection leads to a rapid and non-destructive analysis of Uranium and Thorium. The maximum sensitivity is of 78 ng for Uranium and of 160 ng for Thorium. The Uranium and Thorium dosing based on 239-Np and 233-Pa detection needs chemical selective separations for each of these radionuclides. The liquid-liquid extraction has permitted to elaborate rapid and quantitative separation methods. The sensitivities of the analysis after extraction reach 30 ng for Uranium and 50 ng for Thorium. The fission products separation study has allowed to elaborate the La, Ce and Nd extractions and its application to the Uranium dosing gives satisfying results. A rapid dosing method with a sensitivity of 0.35 microgramme has been elaborated with the help of delayed neutrons measurement. These different methods have been applied to the Uranium and Thorium dosing in samples coming from Oklo mine in Gabon. The analyses of these samples by atomic absorption spectroscopy and by the proton induced X-ray emission (PIXE) method confirm that the neutron activation analysis methods are reliable. 37 figs., 14 tabs., 50 refs

  6. Uranium as Raw Material for Nuclear Energy

    International Nuclear Information System (INIS)

    Lelek, V.

    2006-01-01

    There is lot of information bringing our attention to the problem of limited raw material resources. Fortunately uranium for nuclear energy is very concentrated source and that is why its transport brings no problems and could be realized from anywhere. Second question is if overall resources are available for current nuclear energy development. Data documenting reasons for nowadays price growth are presenting and it is clearly shown that the most probable explanation is that there is gap in new uranium mines preparation and the lot of smaller mines were closed in the period of low uranium prices. Conclusion is that there is at least for the first half of this century even for thermal reactors enough uranium. Situation could be changed if there will massive production of liquid fuel using hydrogen, produced through nuclear heating. Public information about former military uranium resources are also included. Contemporary about one half of US nuclear power-stations is using high enriched uranium diluted with natural uranium - it is expected to continue this way up to 2012. Uranium is complicated market (Authors)

  7. Contribution to the study of liquid-liquid extraction dynamics in the case of fast transfers. Extractions of uranium, plutonium and neptunium in a laboratory centrifugal extractor

    International Nuclear Information System (INIS)

    Bergeonneau, Philippe

    1978-01-01

    The liquid-liquid extraction (also named solvent-based extraction) is a very important technique for the reprocessing of irradiated nuclear fuels. This research thesis is based on the use of a laboratory centrifugal extractor which allows interesting conditions to be achieved: fast transfer due to an intense solution mixing, very short duration of contact between solutions. Thus, after a report of a bibliographical study on chemical mechanisms of extraction, on the composition of extracted species, on extraction kinetics, and on centrifugal extractors, this thesis reports the design, fabrication and use of a centrifugal extractor: presentation of fundamental principles, description and characteristics (materials, hydrodynamic operation test and problems, prototype). It reports studies of fast transfer kinetics: mathematical processing, result interpretation, results and discussions of extraction kinetics for nitric acid, uranium VI and IV, plutonium IV, neptunium IV, and comparison of the different extraction kinetics

  8. Commercial experimental on bacteria heap leaching of uranium ore from Caotaobei mining area in Ganzhou uranium mine

    International Nuclear Information System (INIS)

    Fan Baotuan; Meng Yunsheng; Liu Jian; Xiao Jinfeng; Chen Sencai; Cao Jianbo; Wu Yichang; Liu Chengwu

    2002-01-01

    The author presents the result of commercial experiment on bacteria heap leaching of uranium ore from Caotaobei mining area in Ganzhou Uranium Mine and summarizes the heap situation, installation of spraying and sprinkling devices, and operation management of continuous oxidizing tank of bio-membrane. The leaching rate is 92.95% and 91.88% respectively by liquid and residue measurement during 85 d bacterial leaching experiment. The acid consumption is 2.1% and the total liquid-solid ratio is 2.9 m 3 /t. Compared with conventional heap leaching, the time of bacteria heap leaching shorted about 75 d, the acid consumption reduced by 0.35% and the leaching rate improved by 2%. It is an optimize plan to reform the heap leaching technology for Caotaobei ore

  9. Plant start-up operation of treatment of liquid radioactive waste containing uranium in sulfuric acid by means of ion exchange

    International Nuclear Information System (INIS)

    Bustamante Escobedo, Mauricio

    2003-01-01

    The hydrometallurgy of uranium developed by CCHEN in the '80s generated different types of liquid radioactive waste: organic and aqueous, which have to be treated to extract the uranium, obtaining uranium concentrate less than 3 [ppm], in order to comply with the current regulations and to be able to be discharged as industrial waste over to specialized companies. The radioactive wastes were treated using strongly basic ion exchange resins to obtain a lower volume of concentrated uranium in solid phase. Batch processes were carried out with different pH values (1.4-1.6-1.7-1-8 and 2.0) and different residence times (5-10-15-240 [min]), to define the optimum processing conditions. Three resins were used: IONAC, AFP-329, IONAC A-641, DOWEX 11. The load capacities for each one were: 2[g/l], 1.85 [g/l] and 2.1 [g/l], respectively. Dowex 11 obtained the best uranium load results. Because of the nature of the treated solutions, the pH variation with sodium hydroxide generated precipitation and then crystallization of the existing pieces. Ninety-five percent of the resin's maximum load was attained after about 20 [min] of residence time. Continuous tests were carried out at the solution's original pH to verify the results obtained in the batch stage. This ion exchange process was compared with the chemical precipitation, with lime and sodium hydroxide as well as evaporation and in both processes the volumes of solid that were generated were significantly greater. The ion exchange plant worked with two serially connected columns, using 10 [l] of Dowex 11 resin in each one, with a residence time of 20 [min] per column. A total of 8 [m 3 ] of solution, obtaining an effluent with a uranium concentrate of less than 3 [ppm], using 140 [l] of resin, which generated an average load of 3 [g/l] of uranium (au)

  10. Application of Calixarenes as Macrocyclic Ligands for Uranium(VI: A Review

    Directory of Open Access Journals (Sweden)

    Katarzyna Kiegiel

    2013-01-01

    Full Text Available Calixarenes represent a well-known family of macrocyclic molecules with broad range of potential applications in chemical, analytical, and engineering materials fields. This paper covers the use of calixarenes as complexing agents for uranium(VI. The high effectiveness of calix[6]arenes in comparison to other calixarenes in uranium(VI separation process is also presented. Processes such as liquid-liquid extraction (LLE, liquid membrane (LM separation, and ion exchange are considered as potential fields for application of calixarenes as useful agents for binding UO22+ for effective separation from aqueous solutions containing other metal components.

  11. 75 FR 12738 - Proposed Subsequent Arrangement

    Science.gov (United States)

    2010-03-17

    ... the retransfer of 302,188 kg of U.S.-origin natural uranium trioxide (UO3) (82.73% U), 250,000 kg of which is uranium, from Cameco in Saskatoon, Saskatchewan, Canada to Springfields Fuels Ltd. in... transferred to Springfields Fuels Ltd. for conversion to uranium hexafluoride (UF6) for ultimate end use in a...

  12. Uranium and thorium mining and milling: material security and risk assessment

    International Nuclear Information System (INIS)

    Steinhaeusler, F.; Zaitseva, L.

    2005-01-01

    Full text: At present physical protection for the front end of the nuclear fuel cycle is typically at a significantly lower level than at any other part of the nuclear fuel cycle. In view of past experiences (Israel, South Africa, Pakistan, India) it is feasible to take into consideration some generic threat scenarios, potentially resulting in loss of control over uranium or thorium, respectively their concentrates, such as: illegal mining of an officially closed uranium- or thorium mine; covert diversion of uranium- or thorium ore whilst officially mining another ore; covert transport of radioactive ore or product, using means of public rail, road, ship, or air transport; covert en route diversion of an authorized uranium- or thorium transport; covert removal of uranium-or thorium ore or concentrate from an abandoned facility. The Stanford-Salzburg database on nuclear smuggling, theft, and orphan radiation sources (DSTO) contains information on trafficking incidents involving mostly uranium, but also some thorium, from 30 countries in five continents with altogether 113 incidents in the period 1991 to 2004. These activities range from uranium transported in backpacks by couriers in Afghanistan, to a terrorist organization purchasing land in order to mine covertly for uranium in Australia, and the clandestine shipment of almost two tons of uranium hexafluoride from Asia to Africa, using the services of a national airline. Potential participants in such illegal operations range from entrepreneurs to members of organized crime, depending on the level of sophistication of the operation. End-users and 'customers' of such illegal operations are suspected to be non-state actors, organizations or governments involved in a covert operation with the ultimate aim to acquire a sufficient amount of nuclear material for a nuclear device. The actual risk for these activities to succeed in the acquisition of an adequate amount of suitable radioactive material depends on one or

  13. Degradation and dielectric properties of sulfur hexafluoride

    International Nuclear Information System (INIS)

    Fluck, Eric

    1985-01-01

    Sparking potential of sulfur hexafluoride is studied as a function of its decomposition by electrical discharges. The analysis of the gas is performed by mass spectrometry. The quantity of products resulting from spark discharges as a function of charge transported is plotted for SO_2F_2, SiF_4, SOF_4; it shows a linear increase with charge transported. Production rates of fluoride gases strongly increase with quantity of water vapor present at the beginning of the spark discharges. Decomposition of the gas, even at high levels (20%) does not exhibit measurable variations of sparking potential (at constant pressure). Production of SiF_4 by degradation of glass walls by hydrofluoric acid produced by discharges shows the important role played by this acid in the decomposition of the gas. It is necessary to use a gas containing water impurities at a level as small as possible. (author)

  14. Uranium and thorium migration under dislocative metamorphism

    International Nuclear Information System (INIS)

    Titov, V.K.; Bilibina, T.V.; Dashkova, A.D.; Il'in, V.K.; Makarova, L.I.; Shmuraeva, L.Ya.

    1978-01-01

    Investigated were peculiarities of uranium and thorium behaviour in the process of dislocation metamorphism on the basis of regional fracture zones of early-proterozoic embedding of Ukrainian, Aldan and Baltic shields. The studied zones correspond to tectonite of green-shale and almandin-amphibolite facies of regional metamorphism according to mineral associations. The most peculiar feature of the tectonites of green-shale facies is uranium presence in migrationally able forms, which can be involved afterwards into the ore process by hydrothermal solutions. Adsorved forms of uranium on the crystal surface or separate grains and in the cracks, as well as microinclusions of uranium minerals, selectively timed to mineral structure defects prevail among easily mobile uranium compounds. Dissolved uranium is present, evidently in gas-liquid inclusions in minerals and pore waters. There forms of uranium presence are peculiar for epidote-chlorite mylonites, as well as cataclasites and diaphthorites related to them by blastomylonites of almandin-amphibolite facies. Wide range of manifestation of this process, caused by multikilometer extension of deep fracture zones permit to consider the formations of green-shale facies of dislocation metamorphism as one of the main uranium sources in deposit formation in different uranium-ore associations different age

  15. Review of recent developments in uranium extraction technology

    International Nuclear Information System (INIS)

    Alfredson, P.G.; Crawford, R.E.; Ring, R.J.

    1978-12-01

    Developments in uranium ore processing technology since the AAEC Symposium on Uranium Processing in July 1972 are reviewed. The main developments include the use of autogenous or semi-autogenous grinding, beneficiation techniques such as radiometric sorting, flotation, magnetic and gravity seperation, strong acid and ferric bacterial leaching processes, solution mining and heap leaching operations, horizontal belt filters for solid-liquid separation, continuous ion exchange processes for use with solutions containing up to 8 wt % solids, hydrogen peroxide and ammonia for the precipitation of uranium to improve product yield and purity, and the recovery of by-product uranium from the manufacture of phosphoric acid and copper processing operations

  16. In situ leaching of uranium in South Australia

    International Nuclear Information System (INIS)

    Matthews, D.

    1998-01-01

    The proposed two new uranium mines at Beverley and Honeymoon, South Australia plan to use the cheap but potentially polluting process of in situ leaching (ISL) and permission has already been given for experimental underground leaching at Beverley. The mining industry describes ISL as environmentally benign because, instead of excavating, a corrosive liquid such as sulphuric acid is used. The liquid, sometimes 10000 times more acid than the aquifer water, is pumped into the ground in order to leach out the uranium and the resulting solution is then pumped to the surface where the uranium is extracted. Because the groundwater is salty and radioactive, the mining companies regard it as useless, so its contamination by ISL is considered of no concern. Salty radioactive water can be purified or desalinated and such processes are commonly used by mining companies such as Western Mining Corporation at Roxby Downs. (author)

  17. Hydrofluoric Acid Corrosion Testing on Unplated and Electroless Gold-Plated Samples

    International Nuclear Information System (INIS)

    Osborne, P.E.; Icenhour, A.S.; Del Cul, G.D.

    2000-01-01

    The Molten Salt Reactor Experiment (MSRE) remediation requires that almost 40 kg of uranium hexafluoride (UF6) be converted to uranium oxide (UO). In the process of this conversion, six moles of hydrofluoric acid (HP) are produced for each mole of UF6 converted

  18. Treatment of uranium contaminated wastewater – a review

    International Nuclear Information System (INIS)

    Dulama, M.; Iordache, M.; Deneanu, N.

    2013-01-01

    The paper presents a study of the treatment techniques used for uranium recovery from aqueous solutions, such as: precipitation, ion exchange processes, sorption processes, solvent extractions, separation by liquid membrane, nanofiltration and reverse osmosis. The necessary elements for rigorous treatment experiments that can be used to define innovative procedure for uranium contaminated wastewater treatment are described in this review. The published data were summarized and the areas for further research were identified in order to be able to propose an environmental friendly technology in the field of uranium production and recovery cycle. (authors)

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

    International Nuclear Information System (INIS)

    1994-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

    1994-01-01

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

  1. Investigations into the operating behavior of separation nozzle cascades for uranium-235 enrichment in a 10-stage pilot plant

    International Nuclear Information System (INIS)

    Bley, P.; Hein, H.; Linder, G.

    1984-03-01

    The separation nozzle method developed by the Karlsruhe Nuclear Research Center is based on the centrifugal force in a curved jet consisting of uranium hexafluoride and a light auxiliary gas. To determine in experiments the operating and controlling behavior of separation nozzle cascades a 10-stage pilot plant was erected some year ago. This plant was transferred to the Centro de Desenvolvimento da Tecnologia Nuclear (CDTN) in Belo Horizonte as a donation made within the framework of the German-Brazilian Agreement on scientific cooperation in the field of uranium enrichment. The plant previously equipped with single deflection systems was modified to operate with the double deflection system envisaged for commercial plants. A controlling concept meanwhile developed and improved for separation nozzle cascades equipped with single and double deflection systems was verified experimentally and optimized at the pilot plant of the CDTN. A comparison of the experimental operating behavior with the operating behavior calculated by simulation programs has confirmed the faithfulness of simulation of the computer codes developed to apply to cascades with double deflection systems as well. (orig.) [de

  2. Proserpine - plutonium 239 - Proserpine - uranium 235 - comparison of experimental results; Proserpine - plutonium 239 - proserpine - uranium 235 - comparaison de resultats experimentaux

    Energy Technology Data Exchange (ETDEWEB)

    Brunet, J P; Caizergues, R; Clouet D' Orval, Ch; Kremser, J; Moret-Bailly, J; Verriere, Ph [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1964-07-01

    The Proserpine homogeneous reactor is constituted by a tank, 25 cm dia, 30 cm high, surrounded by a composite reflector made of beryllium oxide and graphite. In this tank can be made critical plutonium or 90 per cent enriched uranium solutions, the fissile substances being in the form of a dissolved salt. In varying the concentration of the solution, critical masses were studied as a function of the level of the liquid in the tank. The minimum critical mass is 256 {+-} 2 grs for plutonium and 409 {+-} 3 grs for uranium 235. In the range of the critical concentrations which were studied, the neutronic properties of fissionable solutions of plutonium and enriched uranium were compared for identical geometries. (authors) [French] Proserpine est un reacteur homogene comportant une cuve de diametre 25 cm, de hauteur 30 cm, entouree d'un reflecteur composite d'oxyde de beryllium et de graphite. On y a rendu critiques des solutions de plutonium ou d'uranium enrichi a 90 pour cent, le produit fissile se trouvant sous la forme d'un sel dissous. En faisant varier la concentration de la solution, on a etudie les masses critiques en fonction de la hauteur du liquide dans la cuve. La masse- critique minimum est, pour le plutonium de 256 {+-} 2 g, pour l'uranium 235 de 409 {+-} 3 g. Dans la gamme des concentrations critiques etudiees, on a compare, dans des conditions de geometrie identique, les proprietes neutroniques des solutions fissiles de plutonium et d'uranium enrichi. (auteurs)

  3. Thermodynamics of the vaporization of uranium tetrabromide

    International Nuclear Information System (INIS)

    Singh, Z.; Prasad, R.; Venugopal, P.V.; Roy, K.N.; Sood, D.D.

    1981-01-01

    Vapour pressures of solid and liquid uranium tetrabromide have been measured in the temperature range of 696 to 805 K and 805 to 1003 K respectively by transpiration and evaporation-temperature techniques. The vapour pressures obtained by the two techniques are in good agreement and have been combined to give the reported vapour-pressure equations for solid and liquid uranium tetrabromide. The melting temperature, the normal boiling temperature, the standard enthalpy of vaporization ΔH 0 (vap, 298.15 K), and the standard entropy of vaporization ΔS 0 (vap, 298.15 K) are reported. The enthalpy of fusion ΔH 0 (fus, 802 K) is also reported. The thermodynamic quantities from the present study are compared with those in the literature and critically analysed. (author)

  4. Combination of solid phase extraction and dispersive liquid–liquid microextraction for separation/preconcentration of ultra trace amounts of uranium prior to its fiber optic-linear array spectrophotometry determination

    International Nuclear Information System (INIS)

    Dadfarnia, Shayessteh; Shabani, Ali Mohammad Haji; Shakerian, Farid; Shiralian Esfahani, Golnaz

    2013-01-01

    Graphical abstract: Pass the sample through the basic alumina column ⇒ elute retained uranium along with the cations ⇒ convert the uranium to its anionic benzoate complex ⇒ extract its ion pair with malachite green into small volume of chloroform by DLLME ⇒ measure its absorption at 621 nm using fiber optic-linear array detection spectrophotometry. -- Highlights: • By combination of SPE and DDLME a high preconcentration factor of 2500 was obtained. • Development of SPE-DDLME-Spectrophotometric method for det. of trace amounts of uranium. • Ultra trace amount of uranium in water samples was det. by the proposed method. • The detection limit of the proposed method is comparable to the most sensitive method. • The proposed method is a free interference spectrophotometric method for uranium det. -- Abstract: A simple and sensitive method for the separation and preconcentration of the ultra trace amounts of uranium and its determination by spectrophotometry was developed. The method is based on the combination of solid phase extraction and dispersive liquid–liquid microextraction. Thus, by passing the sample through the basic alumina column, the uranyl ion and some cations are separated from the sample matrix. The retained uranyl ion along with the cations are eluted with 5 mL of nitric acid (2 mol L −1 ) and after neutralization of the eluent, the extracted uranyl ion is converted to its anionic benzoate complex and is separated from other cations by extraction of its ion pair with malachite green into small volume of chloroform using dispersive liquid–liquid microextraction. The amount of uranium is then determined by the absorption measurement of the extracted ion pair at 621 nm using flow injection spectrophotometry. Under the optimum conditions, with 500 mL of the sample, a preconcentration factor of 1980, a detection limit of 40 ng L −1 , and a relative standard deviation of 4.1% (n = 6) at 400 ng L −1 were obtained. The method was

  5. Uranium recovery from wet-process phosphoric acid

    International Nuclear Information System (INIS)

    McCullough, J.F.; Phillips, J.F. Jr.; Tate, L.R.

    1979-01-01

    A method of recovering uranium from wet-process phosphoric acid is claimed where the acid is treated with a mixture of an ammonium salt or ammonia, a reducing agent, and then a miscible solvent. Solids are separated from the phosphoric acid liquid phase. The solid consists of a mixture of metal phosphates and uranium. It is washed free of adhering phosphoric acid with fresh miscible solvent. The solid is dried and dissolved in acid whereupon uranium is recovered from the solution. Miscible solvent and water are distilled away from the phosphoric acid. The distillate is rectified and water discarded. All miscible solvent is recovered for recycle. 5 claims

  6. Generic report on health effects for the US Gaseous Diffusion Plants. Sect. 8, Pt. 1

    International Nuclear Information System (INIS)

    Just, R.A.; Emler, V.S.

    1984-06-01

    Toxic substances present in uranium enrichment plants include uranium hexafluoride (UF 6 ), hydrogen fluoride (HF), uranyl fluoride (UO 2 F 2 ), chlorine (Cl 2 ), chlorine trifluoride (ClF 3 ), fluorine (F 2 ), uranium tetrafluoride (UF 4 ), and technetium (Tc). The current knowledge of the expected health effects of acute exposures to these substances is described. 10 references, 2 figures, 6 tables

  7. Uncontrolled transport of nuclear materials

    International Nuclear Information System (INIS)

    Wassermann, U.

    1985-01-01

    An account is given of international transport of plutonium, uranium oxides, uranium hexafluoride, enriched uranium and irradiated fuel for reprocessing. Referring to the sinking of the 'Mont Louis', it is stated that the International Maritime Organization has been asked by the National Union of Seamen and 'Greenpeace' to bar shipment of radioactive material until stricter international safety regulations are introduced. (U.K.)

  8. Semitechnical studies of uranium recovery from wet process phosphoric acid by liquid-liquid-extraction method

    International Nuclear Information System (INIS)

    Poczynajlo, A.; Wlodarski, R.; Giers, M.

    1987-01-01

    A semitechnical installation for uranium recovery from wet process phosphoric acid has been built. The installation is based on technological process comprising 2 extraction cycles, the first with a mixture of mono- and dinonylphenylphosphoric acids (NPPA) and the second with a synergic mixture of di-/2-ethylhexyl/-phosphoric acid (D2EHPA) and trioctylphosphine oxide (TOPO). The installation was set going and the studies on the concentration distributions of uranium and other components of phosphoric acid have been performed for all technological circuits. 23 refs., 15 figs., 3 tabs. (author)

  9. Alpha spectrometry enriched uranium urinalysis results from IPEN

    International Nuclear Information System (INIS)

    Lima, Marina Ferreira

    2008-01-01

    Full text: IPEN (Instituto de Pesquisas Energeticas e Nucleares) manufactures the nuclear fuel to its research reactor, the IEA-R1. The CCN (Centro do Ciclo do Combustivel) facility produces the fuel cermets from UF 6 (uranium hexafluoride) enriched to 19.75% in 235 U. The production involves the transformation of the gaseous form in oxides and silicates by ceramic and metallurgical processing. The workers act in more than one step that involves exposition to types F, S and M compounds of uranium. Until 2003, only fluorimetric analysis was carried out by the LRT (Laboratorio de Radiotoxicologia - IPEN) in order to evaluate the intake of uranium, in spite of the sub estimation of the 234 U contribution to the internal doses. Isotopic uranium determination in urine by alpha spectrometry is the current method to monitoring the contribution of 234 U, 235 U and 238 U. Alpha spectrometry data of 164 samples from 84 individuals separate in three categories of workers: routinely work group; special operation group and control group - were analyzed how the isotopic composition excreted by urinary tract corresponds with the level of enrichment and isotopic composition of the plant products. Results show that is hard to estimate these intakes of 234 U and 235 U since these isotopes alpha activities are below the limit of detection or minimum detectable activity (MAD) of this method in the most part of the samples. Only in 22 samples it was possibly to measure the three radionuclides. Not expected high contribution of 234 U activity was found in samples of the control group. No one result over the 234 U and 235 U MAD was found in the samples from the special operation group. Only in 5 samples from the routinely group the levels of 235 U was higher than the levels of others groups. In a complementary study, 3 solid samples of UF 6 , U 2 O 8 and U 3 Si 2 from CCN plant were analyzed to determinate the isotopic uranium composition in these salts, since this composition varies

  10. Recovery of uranium from biological adsorbents - desorption equilibrium

    International Nuclear Information System (INIS)

    Tsezos, M.

    1984-01-01

    Results are presented of the experimental investigations of uranium elution and reloading for the waste inactive biomass of Rhizopus arrhizus. The experimental data and the analysis of the present work suggest the following conclusions: recovery of uranium that has been taken up by R. arrhizus is possible by elution; of the six elution systems examined, sodium bicarbonate solutions appear to be the most promising because they can effect near complete uranium recovery and high uranium concentration factors; the bicarbonate solution causes the least damage to the biomass; solid-to-liquid ratios in bicarbonate elution systems can exceed 120:1 (mg:mL) for a 1N NaHCO 3 solution, with almost complete uranium recovery and eluate uranium concentrations of over 1.98 x 10 4 mg/L; mineral acids, although good elution agents, result in substantial damage to the biomass thus limiting the biomass reuse potential; sulfate ions in the elutions solution limit the elution potential of the biomass, possibly by conferring novel crystallinity to the cell wall chitin network and confining inside the chitin network more biosorbed uranium

  11. Technology for Treatment of Liquid Radioactive Waste Generated during Uranium and Plutonium Chemical and Metallurgical Manufacturing in FSUE PO Mayak - 13616

    Energy Technology Data Exchange (ETDEWEB)

    Adamovich, D. [SUE MosSIA Radon, 2/14 7th Rostovsky lane, Moscow, 119121 (Russian Federation); Batorshin, G.; Logunov, M.; Musalnikov, A. [FSUE ' PO Mayak' , 31 av. Lenin, Ozyorsk, Chelyabinsk region, 456780 (Russian Federation)

    2013-07-01

    Created technological scheme for treatment of liquid radioactive waste generated while uranium and plutonium chemical and metallurgical manufacturing consists of: - Liquid radioactive waste (LRW) purification from radionuclides and its transfer into category of manufacturing waste; - Concentration of suspensions containing alpha-nuclides and their further conversion to safe dry state (calcinate) and moving to long controlled storage. The following technologies are implemented in LRW treatment complex: - Settling and filtering technology for treatment of liquid intermediate-level waste (ILW) with volume about 1500m{sup 3}/year and alpha-activity from 10{sup 6} to 10{sup 8} Bq/dm{sup 3} - Membrane and sorption technology for processing of low-level waste (LLW) of radioactive drain waters with volume about 150 000 m{sup 3}/year and alpha-activity from 10{sup 3} to 10{sup 4} Bq/dm{sup 3}. Settling and filtering technology includes two stages of ILW immobilization accompanied with primary settling of radionuclides on transition metal hydroxides with the following flushing and drying of the pulp generated; secondary deep after settling of radionuclides on transition metal hydroxides with the following solid phase concentration by the method of tangential flow ultrafiltration. Besides, the installation capacity on permeate is not less than 3 m{sup 3}/h. Concentrates generated are sent to calcination on microwave drying (MW drying) unit. Membrane and sorption technology includes processing of averaged sewage flux by the method of tangential flow ultrafiltration with total capacity of installations on permeate not less than 18 m{sup 3}/h and sorption extraction of uranium from permeate on anionite. According to radionuclide contamination level purified solution refers to general industrial waste. Concentrates generated during suspension filtering are evaporated in rotary film evaporator (RFE) in order to remove excess water, thereafter they are dried on infrared heating

  12. Uranium mill tailings regulation and the generic environmental impact statement

    International Nuclear Information System (INIS)

    Rogers, V.C.

    1980-01-01

    The following topics are discussed: the history of the Canadian uranium industry; the Canadian management of uranium mining wastes; Canadian federal and provincial effluent guidelines for radium-226; tailings and mine water management; backfill; liquid effluents from tailings storage; barium chloride treatment; mine water (Fay Mine); mine water (Dubyna Mine); and revegetation. 22 refs

  13. Environmental impact of uranium mining and milling in Australia

    International Nuclear Information System (INIS)

    Levins, D.M.

    1980-01-01

    Australia has almost twenty per cent of the Western World's low-cost uranium reserves, located mostly in the Alligator Rivers region of the Northern Territory. At present, only one uranium mill is operating in Australia, but a number of new mills are planned for the early 1980s. Details are given of Australian uranium mining and milling proposals and the measures taken to minimize their environmental impact. Major factors affecting environmental impact are discussed, including treatment of liquid wastes, water management, control of radon and other airborne releases, and disposal of tailings. (auth)

  14. Investigation of applications for high-power, self-critical fissioning uranium plasma reactors. Final technical report

    International Nuclear Information System (INIS)

    Rodgers, R.J.; Latham, T.S.; Krascella, N.L.

    1976-09-01

    Analytical studies were conducted to investigate potentially attractive applications for gaseous nuclear cavity reactors fueled by uranium hexafluoride and its decomposition products at temperatures of 2000 to 6000 K and total pressures of a few hundred atmospheres. Approximate operating conditions and performance levels for a class of nuclear reactors in which fission energy removal is accomplished principally by radiant heat transfer from the high temperature gaseous nuclear fuel to surrounding absorbing media were determined. The results show the radiant energy deposited in the absorbing media may be efficiently utilized in energy conversion system applications which include (1) a primary energy source for high thrust, high specific impulse space propulsion, (2) an energy source for highly efficient generation of electricity, and (3) a source of high intensity photon flux for heating working fluid gases for hydrogen production or MHD power extraction. (Author)

  15. The nuclear fuel cycle

    International Nuclear Information System (INIS)

    1998-05-01

    After a short introduction about nuclear power in the world, fission physics and the French nuclear power plants, this brochure describes in a digest way the different steps of the nuclear fuel cycle: uranium prospecting, mining activity, processing of uranium ores and production of uranium concentrates (yellow cake), uranium chemistry (conversion of the yellow cake into uranium hexafluoride), fabrication of nuclear fuels, use of fuels, reprocessing of spent fuels (uranium, plutonium and fission products), recycling of energetic materials, and storage of radioactive wastes. (J.S.)

  16. The nuclear fuel cycle; Le cycle du combustible nucleaire

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-05-01

    After a short introduction about nuclear power in the world, fission physics and the French nuclear power plants, this brochure describes in a digest way the different steps of the nuclear fuel cycle: uranium prospecting, mining activity, processing of uranium ores and production of uranium concentrates (yellow cake), uranium chemistry (conversion of the yellow cake into uranium hexafluoride), fabrication of nuclear fuels, use of fuels, reprocessing of spent fuels (uranium, plutonium and fission products), recycling of energetic materials, and storage of radioactive wastes. (J.S.)

  17. Determination of uranium in clinical and environmental samples by FIAS-ICPMS

    International Nuclear Information System (INIS)

    Karpas, Z.; Lorber, A.; Halicz, L.; Gavrieli, I.

    1998-01-01

    Uranium may enter the human body through ingestion or inhalation. Ingestion of uranium compounds through the diet, mainly drinking water, is a common occurrence, as these compounds are present in the biosphere. Inhalation of uranium-containing particles is mainly an occupational safety problem, but may also take place in areas where uranium compounds are abundant. The uranium concentration in urine samples may serve as an indication of the total uranium body content. A method based on flow injection and inductively coupled plasma mass spectrometry (FIAS-ICPMS) was found to be most suitable for determination of uranium in clinical samples (urine and serum), environmental samples (seawater, wells and carbonate rocks) and in liquids consumed by humans (drinking water and commercial beverages). Some examples of the application of the FIAS-ICPMS method are reviewed and presented here

  18. The Ellweiler uranium plant - a demolition and recycling project

    International Nuclear Information System (INIS)

    Mika, S.; Rohr, T.; Seehars, R.; Feser, A.

    1999-01-01

    The uranium plant at Ellweiler, district of Birkenfeld, was used for the production and storage of uranium concentrates. The owner of the Ellweiler uranium plant (UAE), Gewerkschaft Brunhilde GmbH, ceased processing uranium ore and recycling in 1989 and has been in liquidation since September 1991. The State of Rhineland-Palatinate, had safety measures adopted in a first step, getting the plant into a safe state by former plant personnel. The entire plant was demolished in a second step. The contract for demolishing the former uranium plant was awarded to ABB Reaktor as the general contractor in August 1996. Demolition work was carried out between April 1997 and May 1999. A total of approx. 7900 Mg of material was disposed of. At present, recultivation measures are being carried out. (orig.) [de

  19. Recovery of uranium from the Syrian phosphate by solid-liquid method using alkaline solutions

    International Nuclear Information System (INIS)

    Shlewit, H.; Alibrahim, M.

    2007-01-01

    Uranium concentrations were analyzed in the Syrian phosphate deposits. Mean concentrations were found between 50 and 110 ppm. As a consequence, an average phosphate dressing of 22 kg/ha phosphate would charge the soil with 5-20 g/ha uranium when added as a mineral fertilizer. Fine grinding phosphate produced at the Syrian mines was used for uranium recovery by carbonate leaching. The formation of the soluble uranyl tricarbonate anion UO 2 (CO 3 ) 3 4- permits use of alkali solutions of sodium carbonate and sodium bicarbonate salts for the nearly selective dissolution of uranium from phosphate. Separation of iron, aluminum, titanium, etc., from the uranium during leaching was carried out. Formation of some small amounts of molybdates, vanadates, phosphates, aluminates, and some complexes metal was investigated. This process could be used before the manufacture of TSP fertilizer, and the final products would contain smaller uranium quantities. (author)

  20. Field test of short-notice random inspections for inventory-change verification at a low-enriched-uranium fuel-fabrication plant: Preliminary summary

    International Nuclear Information System (INIS)

    Fishbone, L.G.; Moussalli, G.; Naegele, G.; Ikonomou, P.; Hosoya, M.; Scott, P.; Fager, J.; Sanders, C.; Colwell, D.; Joyner, C.J.

    1994-01-01

    An approach of short-notice random inspections (SNRIs) for inventory-change verification can enhance the effectiveness and efficiency of international safeguards at natural or low-enriched uranium (LEU) fuel fabrication plants. According to this approach, the plant operator declares the contents of nuclear material items before knowing if an inspection will occur to verify them. Additionally, items about which declarations are newly made should remain available for verification for an agreed time. This report details a six-month field test of the feasibility of such SNRIs which took place at the Westinghouse Electric Corporation Commercial Nuclear Fuel Division. Westinghouse personnel made daily declarations about both feed and product items, uranium hexafluoride cylinders and finished fuel assemblies, using a custom-designed computer ''mailbox''. Safeguards inspectors from the IAEA conducted eight SNRIs to verify these declarations. Items from both strata were verified during the SNRIs by means of nondestructive assay equipment. The field test demonstrated the feasibility and practicality of key elements of the SNRI approach for a large LEU fuel fabrication plant

  1. Cost-effectiveness of safety measures to reduce public risk associated with the transportation of UF{sub 6} by truck and trains

    Energy Technology Data Exchange (ETDEWEB)

    Hubert, Philippe; Pages, Pierre

    1989-08-01

    The present case study deals with the problem of uranium hexafluoride transportation by truck and train. It consists of a probabilistic risk assessment of the potential hazards to the public that can arise from the traffic that will take place in France in 1990. The specificity of UF{sub 6} is that it presents both chemical and radiological hazards. But, whatever the transported material, road traffic entails a risk of its own. Thus three kinds of risks are assessed for natural, depleted and enriched uranium hexafluoride. These assessments are the basis of a cost-effectiveness analysis which deals with such safety measures as using a protective overpack, avoiding populated areas and escorting the trucks.

  2. Cost-effectiveness of safety measures to reduce public risk associated with the transportation of UF6 by truck and trains

    International Nuclear Information System (INIS)

    Hubert, Philippe; Pages, Pierre

    1989-01-01

    The present case study deals with the problem of uranium hexafluoride transportation by truck and train. It consists of a probabilistic risk assessment of the potential hazards to the public that can arise from the traffic that will take place in France in 1990. The specificity of UF 6 is that it presents both chemical and radiological hazards. But, whatever the transported material, road traffic entails a risk of its own. Thus three kinds of risks are assessed for natural, depleted and enriched uranium hexafluoride. These assessments are the basis of a cost-effectiveness analysis which deals with such safety measures as using a protective overpack, avoiding populated areas and escorting the trucks

  3. Process control of a gaseous diffusion cascade for isotopic separation of uranium

    International Nuclear Information System (INIS)

    Bilous, Olegh; Doneddu, F.

    1986-01-01

    Various aspects of dynamics and process control of a gaseous diffusion cascade are described. The cascade enriches uranium hexafluoride gas (HEX) in the light isotope of uranium in a countercurrent flow. The linearized equations describing the equipment models are derived. One can then write the mass balances on the high and low pressure sides of a stage and the overall heat balance of a stage. These heat and mass balances are linear difference equations on the stage number with time derivatives which are then replaced by jω factors to examine the effects of cyclic perturbations. The mass balances are first treated for a cascade section of 12 stages with temperatures assumed constant. The effect of a perturbation of pressure on one of the stages is described first for ω=0 (that is for steady state). Then Nyquist diagrams are obtained. The effect of transport change is also studied. Then temperature is introduced, assuming pressures to be constant. The cases of a section of 12 stages and a cascade of 120 stages are examined. Again Nyquist diagrams of temperature frequency response to a perturbation on one stage are calculated. Process control of the heat exchangers is introduced. The method used to solve the difference equations may be applied to other types of perturbations and to the complete scheme of process control. (author)

  4. Sorption of natural uranium by algerian bentonite

    International Nuclear Information System (INIS)

    Megouda, N.; Kadi, H.; Hamla, M.S.; Brahimi, H.

    2004-01-01

    Full text.Batch sorption experiments have been used to assess the sorption behaviour of uranium onto natural and drilling bentonites. The operating parameters (pH, aolis-liquid ratio, particle size, time and initial uranium concentration) influenced the rate of adsorption. The distribution coefficient (Kd) range values at equilibrium time are 45.95-1079.26 ml/g and 32.81-463053 ml/g for the drilling and natural bentonites respectively. The equilibrium isotherms show that the data correlate with both Freundlich and Langmuir models

  5. Separation of adhered salt from uranium deposits generated in electro-refiner

    International Nuclear Information System (INIS)

    Kwon, S.W.; Park, K.M.; Lee, H.S.; Kim, J.G.; Ahn, H.G.

    2011-01-01

    It is important to increase a throughput of the salt removal process from uranium deposits which is generated on the solid cathode of electro-refiner in pyroprocess. In this study, it was proposed to increase the throughput of the salt removal process by the separation of the liquid salt prior to the distillation of the LiCl-KCl eutectic salt from the uranium deposits. The feasibility of liquid salt separation was examined by salt separation experiments on a stainless steel sieve. It was found that the amount of salt to be distilled could be reduced by the liquid salt separation prior to the salt distillation. The residual salt remained in the deposits after the liquid salt separation was successfully removed further by the vacuum distillation. It was concluded that the combination of a liquid salt separation and a vacuum distillation is an effective route for the achievement of a high throughput performance in the salt separation process. (author)

  6. Use of a pulsed column with discs and crowns for uranium extraction from phosphoric acid

    International Nuclear Information System (INIS)

    1982-04-01

    The physico-chemistry of the system phosphoric acid-uranium-dioctylpyrophosphoric acid is studied for the determination of analytical methods and extraction parameters (oxidation state of uranium and iron, phosphorus concentration, extractant concentration). Extraction is then realized on a pilot scale with a liquid-liquid extraction column 4m high and of 50 mm in diameter with a column packing made of discs and crowns. Column efficiency is evaluated by studying uranium transfer as a function of operating conditions. The results obtained are extrapolated to an industrial scale and a comparative economic evaluation is made between a pulsed column and a mixer-settler [fr

  7. Liquid-liquid extraction of uranium from Egyptian phosphoric acid using a synergistic D2EHPA-DBBP mixture

    International Nuclear Information System (INIS)

    Abdel-Khalek, A.A.

    2011-01-01

    Extraction of uranium from Egyptian phosphoric acid with synergistic mixture of di-2-ethylhexylphosphoric acid (D2EHPA) and di-butyl butyl phosphonate (DBBP) is reported in this paper. The influence of various factors such as D2EHPA concentration, DBBP concentration, phosphoric acid concentration, contact time, aqueous: organic phase's ratio (aq:org) and temperature on the degree of extraction has been established. The data on the effect of temperature on the extraction showed that the enthalpy change is -23.12 kJ/mol. Uranium extracted by D2EHPA- DBBP is further subjected to a second cycle of extraction and scrubbing impurities. The uranium is finally converted to a high purity UO 3 product using precipitation with hydrogen peroxide and heat treatment at 375 deg C. (author)

  8. Advancing liquid metal reactor technology with nitride fuels

    International Nuclear Information System (INIS)

    Lyon, W.F.; Baker, R.B.; Leggett, R.D.; Matthews, R.B.

    1991-08-01

    A review of the use of nitride fuels in liquid metal fast reactors is presented. Past studies indicate that both uranium nitride and uranium/plutonium nitride possess characteristics that may offer enhanced performance, particularly in the area of passive safety. To further quantify these effects, the analysis of a mixed-nitride fuel system utilizing the geometry and power level of the US Advanced Liquid Metal Reactor as a reference is described. 18 refs., 2 figs., 2 tabs

  9. Laboratory-scale catalysis studies of uranium and plutonium fluorination reactions by solid metal-fluorides

    International Nuclear Information System (INIS)

    Hochel, R.C.

    1984-03-01

    Various catalysts were evaluated for their effect on the rate of fluorination of the tetrafluorides of uranium and plutonium to produce the hexafluorides. Results of this work show that CoF 3 and AgF 2 are more effective than NiF 2 for UF 4 fluorination, producing rate increases in the range of 150 to 300 compared to UF 4 and fluorine alone. The use of these three catalysts was also found effective in the fluorinations of PuO 2 /PuF 4 and pure PuF 4 . However, enhancements were less. NiF 2 produced the best increases which were 8.1 for PuO 2 /PuF 4 and 3.6 for PuF 4 . Experiments were conducted in a simple flow-loop. Even larger enhancements might be obtained with fluidized beds. Details of the apparatus, experiments, methods, and a discussion of results are presented

  10. Reducing emissions from uranium dissolving

    International Nuclear Information System (INIS)

    Griffith, W.L.; Compere, A.L.; Huxtable, W.P.; Googin, J.M.

    1992-10-01

    This study was designed to assess the feasibility of decreasing NO x emissions from the current uranium alloy scrap tray dissolving facility. In the current process, uranium scrap is dissolved in boiling nitric acid in shallow stainless-steel trays. As scrap dissolves, more metal and more nitric acid are added to the tray by operating personnel. Safe geometry is assured by keeping liquid level at or below 5 cm, the depth of a safe infinite slab. The accountability batch control system provides additional protection against criticality. Both uranium and uranium alloys are dissolved. Nitric acid is recovered from the vapors for reuse. Metal nitrates are sent to uranium recovery. Brown NO x fumes evolved during dissolving have occasionally resulted in a visible plume from the trays. The fuming is most noticeable during startup and after addition of fresh acid to a tray. Present environmental regulations are expected to require control of brown NO x emissions. A detailed review of the literature, indicated the feasibility of slightly altering process chemistry to favor the production of NO 2 which can be scrubbed and recycled as nitric acid. Methods for controlling the process to manage offgas product distribution and to minimize chemical reaction hazards were also considered

  11. Study of ion separation through solid-supported liquid membrane

    International Nuclear Information System (INIS)

    Kang, Young Ho; Kim, Jung Do; Kim, Kyoung Ho

    1990-01-01

    The membranes used in this study consist of a microporous polymeric support with the solvent contraining alamine 336, Tri-N-Octyl phosphine oxide, Tri-N-butyl phosphate, Di-(2-ethylhexyl) phosphoric acid as a carrier within the pores by the capillary forces. When this liquid membrane is interposed between aqueous feed and product solutions, the carrier serving as a complexing agent, can pick up the uranium ions on the feed side of the membrane and carry them across the membrane by diffusion. In this study, the uranium flux through the solid-supported liquid membrane was analyzed as a function of carrier concentration and acidity of the feed solution for the carrier species. Also, the Gel-liquid extraction of uranium ions from aqueous solution was performed. The adsorbents were prepared by casting the polymer solution composed of polyvinyl chloride, TOPO, and additions. The extraction of uranyl nitrate ions has been investigated as a function of TOPO/PVC ratio, evaporation time, and the stability. The results show that is maybe possible to develop an alternative uranium purification process. (author)

  12. Thermophysical measurements on liquid metals above 4000 K

    International Nuclear Information System (INIS)

    Shaner, J.W.; Gathers, G.R.; Hodgson, W.M.

    1977-01-01

    Thermophysical data are presented for liquid niobium up to approximately 6000 0 K and for liquid lead up to approximately 5000 0 K. These new results are summarized along with previously obtained high temperature data for liquid molybdenum, tantalum, tungsten, and uranium

  13. Process for recovering uranium from wet process phosphoric acid (III)

    International Nuclear Information System (INIS)

    Pyrih, R.Z.; Rickard, R.S.; Carrington, O.F.

    1983-01-01

    Uranium is conventionally recovered from wet-process phosphoric acid by two liquid ion exchange steps using a mixture of mono- and disubstituted phenyl esters of orthophosphoric acid (OPPA). Efficiency of the process drops as the mono-OPPA is lost preferentially to the aqueous phase. This invention provides a process for the removal of the uranium process organics (OPPA and organic solvents) from the raffinate of the first liquid ion exchange step and their return to the circuit. The process organics are removed by a combination flotation and absorption step, which results in the recovery of the organics on beads of a hydrophobic styrene polymer

  14. The uranium waste fluid processing examination by liquid and liquid extraction method using the emulsion flow method

    International Nuclear Information System (INIS)

    Kanda, Nobuhiro; Daiten, Masaki; Endo, Yuji; Yoshida, Hideaki; Mita, Yutaka; Naganawa, Hirochika; Nagano, Tetsushi; Yanase, Nobuyuki

    2015-03-01

    Spent centrifuges which had used for the development of the uranium enrichment technology are stored in the uranium enrichment facility located in Ningyo-toge Environmental Center, Japan Atomic Energy Agency (JAEA). Our technology of the centrifugal machine processing are supposed to separate the radioactive material adhered on surface of inner parts of centrifuges by the wet way decontamination method using the ultrasonic bath filled dilute sulfuric acid and water, and it is generated the neutralization sediment (sludge) by the processing of the radioactive waste fluid with the decontamination. JAEA had been considering the applicability of a streamlining and reduction of the processing of the sludge by decreases radioactive concentration including the sludge through the removes uranium from the radioactive waste fluid. As part of considerations, JAEA have been promoting technological developments of the uranium extraction separation using The Emulsion Flow Extraction Method (a theory propounded by JAEA-Nuclear Science and Engineering Center) in close coordination and cooperation between with JAEA-Nuclear Science and Engineering Center and Ningyo-toge Environmental Center from 2007 fiscal year. This report describes the outline of the application test using actual waste fluid of dilute sulfuric acid and water by developed the examination system introducing the emulsion flow extraction method. (author)

  15. Development of uranium metal targets for 99Mo production

    International Nuclear Information System (INIS)

    Wiencek, T.C.; Hofman, G.L.

    1993-10-01

    A substantial amount of high enriched uranium (HEU) is used for the production of medical-grade 99 Mo. Promising methods of producing irradiation targets are being developed and may lead to the reduction or elimination of this HEU use. To substitute low enriched uranium (LEU) for HEU in the production of 99 Mo, the target material may be changed to uranium metal foil. Methods of fabrication are being developed to simplify assembly and disassembly of the targets. Removal of the uranium foil after irradiation without dissolution of the cladding is a primary goal in order to reduce the amount of liquid radioactive waste material produced in the process. Proof-of-concept targets have been fabricated. Destructive testing indicates that acceptable contact between the uranium foil and the cladding can be achieved. Thermal annealing tests, which simulate the cladding/uranium diffusion conditions during irradiation, are underway. Plans are being made to irradiate test targets

  16. Application of alkaline leaching to the extraction of uranium from shale of the Vosges

    International Nuclear Information System (INIS)

    Mouret, P.; Pottier, P.; Le Bris, J.

    1958-01-01

    Description of chemical treatment of Vosges shales to obtain uranium by alkaline leaching. Mineralogy aspects of ore, physical and chemical conditions of leaching, solid/liquid separation, uranium recovery by either ion exchange process or electrolytic precipitation. (author) [fr

  17. Guidelines for evaluation of the environmental expense

    International Nuclear Information System (INIS)

    Komatsu, Cintia Nagako; Aquino, Afonso Rodrigues de

    2009-01-01

    The main objective of this research is to establish guidelines to fit the Environment Account in the Nuclear Fuel Cycle, using as study of case the Uranium Hexafluoride Production Unit of Centro Tecnologico da Marinha in Sao Paulo. The environment accounting, branch of the accounting science, supply a source of tools capable to measure the protection efforts, the nature preservation, the environment monitoring and the recovering during all the Conversion phase (since the Uranium concentrated, the yellow cake, up to the Uranium hexafluoride production). It was performed several researches, visits to the Centre, databank creation, interviews and extensive consulting to the preliminary safety report, in order to obtain the percentage of the total expenses related to environment protection in regarding to the total amount invested in the unit. It was also evaluated the total preserved green area making possible a preliminary environment accounting balance. (author)

  18. Guidelines for evaluation of the environmental expense in the nuclear fuel cycle

    International Nuclear Information System (INIS)

    Komatsu, Cintia Nagako

    2008-01-01

    The main objective of this research is to establish guidelines to fit the environment account in the nuclear fuel cycle, using as study of case the uranium hexafluoride production unit of Centro Tecnologico da Marinha in Sao Paulo. The environment accounting, branch of the accounting science, supply a source of tools capable to measure the protection efforts, the nature preservation, the environment monitoring and the recovering during all the conversion phase (since the uranium concentrated, the yellow cake, up to the Uranium hexafluoride production). It was performed several researches, visits to the Centre, databank creation, interviews and extensive consulting to the preliminary safety report, in order to obtain the percentage of the total expenses related to environment protection in regarding to the total amount invested in the unit. It was also evaluated the total preserved green area making possible a preliminary environment accounting balance. (author)

  19. Characteristics of chlorites from Huangnihu uranium deposit and their implications in uranium metallogenic environment in the southern part of Jiangxi Province

    International Nuclear Information System (INIS)

    Hu Zhihua; Lin Jinrong; Pang Yaqing; Gao Fei; Rong Jiashu; Guo Shuying

    2013-01-01

    Chlorite is genetically related to uranium mineralization in Huangnihu uranium deposit. By means of microscopic and electronic microprobe analysis, the authors investigated chemical composition and texture of the chlorite and found that chlorite in Huangnihu deposit has the following characteristics: 1. they are mainly Fe-rich chlorite composed of chamosite and brunsvigite, of which chemical composition is mainly affected by mud and mafic rock; 2. the Fe-Mg and Al"I"V-Si substitution dominates the octahedral substitution supplemented by Al"V"I-Fe substitution; the oolitic chlorite and biotite feinted chlorite closely associated with uranium were formed at temperatures of 216.23 ∼ 256.73℃ (average 228.6℃). The chemical composition and forming environment of the oolitic chlorite and biotite illusion chlorite suggests that Huangnihu uranium deposit is a low-moderate temperature hydrothermal uranium deposit formed in a reducing environment and iron-rich formation, the ore-forming fluid mainly originated from shale rock, partly from ultramafic or mafic liquid. (authors)

  20. Studies on the mechanism for in-place leaching of fragmented uranium ore by blasting

    International Nuclear Information System (INIS)

    Wu Hengshan; Wang Changhan

    2001-01-01

    The report is based on the locale test studies at No.745 Mine and Baifang Copper (Uranium) Mine. According to hydrokinetics of porous medium. The character of mining methods of in-place leaching of fragmented uranium are, the best application conditions, in-place leaching theory, the fittest composite of fragments of crashing uranium ore, the lowest velocity of flow in solution liquid, the reasonable parameter of stop structure, the technology of leaching, meaning, the equation of solution liquid, the name of solution mining and its classification are studied. Especially some creation in the theory of leaching in mud ore and the technology of strengthened leaching are given. It would be helpful to the design and production

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