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...

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

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.

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

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.

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

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

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

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

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

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)

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

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)

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

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

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

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.

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

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

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

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)

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

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)

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

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

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.)

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

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

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

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.

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

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.

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.

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

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

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...

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)

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

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

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

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

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

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

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

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)

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...

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)

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

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

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

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...

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

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)

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

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.

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

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

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.)

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

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

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)

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

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

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

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

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

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.

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

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)

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

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

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)

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

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.

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.

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

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...

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

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

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

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.

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

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

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

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

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

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

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.

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.

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)

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

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)

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

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

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.

Uranium/water vapor reactions in gaseous atmospheres

International Nuclear Information System (INIS)

Jackson, R.L.; Condon, J.B.; Steckel, L.M.

1977-07-01

Experiments have been performed to determine the effect of varying humidities, gaseous atmospheres, and temperatures on the uranium/water vapor reaction. A balance, which allowed continuous in-system weighings, was used to determine the rates of the uranium/water vapor reactions at water vapor pressures of 383, 1586, and 2853 Pa and at temperatures of 80, 100, and 150 0 C in atmospheres of hydrogen, argon, or argon/oxygen mixtures. Based on rate data, the reactions were characterized as hydriding or nonhydriding. Hydriding reactions were found to be preferred in moist hydrogen systems at the higher temperatures and the lower humidities. The presence of hydrogen in hydriding systems was found to initially inhibit the reaction, but causes an acceleration of the rate in the final stages. In general, reaction rates of hydriding systems approached the hydriding rates calculated and observed in dry hydrogen. Hydriding and nonhydriding reaction rates showed a positive correlation to temperature and water vapor pressure. Final reaction rates in moist argon/oxygen mixtures of 1.93, 4.57, and 9.08 mole percent oxygen were greater than the rates observed in moist hydrogen or argon. Final reaction rates were negatively correlated to the oxygen concentration

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)

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

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

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...

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)

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

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)

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

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

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)

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

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)

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...

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

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)

The use of laser diodes for control of uranium vaporization rates

International Nuclear Information System (INIS)

Hagans, K.; Galkowski, J.

1993-09-01

Within the Atomic Vapor Laser Isotope Separation (AVLIS) program we have successfully used the laser absorption spectroscopy technique (LAS) to diagnose process physics performance and control vaporization rate. In the LAS technique, a narrow line-width laser is tuned to an absorption line of the species to be measured. The laser light that is propagated through the sample is and, from this data, the density of the species can be calculated. These laser systems have exclusively consisted of expensive, cumbersome, and difficult to maintain argon-ion-pumped ring dye lasers. While the wavelength flexibility of dye lasers is very useful in a laboratory environment, these laser systems are not well suited for the industrial process control system under development for an AVLIS plant. Diode-lasers offer lower system costs, reduced man power requirements, reduced space requirements, higher system availability, and improved operator safety. We report the. successful deployment and test of a prototype laser diode based uranium vapor rate control system. Diode-laser generated LAS data was used to control the uranium vaporization rate in a hands-off mode for greater than 50 hours. With one minor adjustment the system successfully controlled the vaporization rate for greater than 147 hours. We report excellent agreement with ring dye laser diagnostics and uranium weigh-back measurements

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

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

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

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)

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

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.

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

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)

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...

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)

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.

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.

Thermal decomposition of calcium aluminium phosphate of Thies. [Vaporization of uranium and phosphorus pentoxide

Energy Technology Data Exchange (ETDEWEB)

Allaf, K; Rouanet, A

1984-01-01

This study is related to the work on beneficiation of raw phosphates by thermal processing (selective vaporization). More precisely it deals with the ability of a calcium-aluminium phosphate (ores from Thies) to vaporize selectively as phosphorus pentoxide and uranium contents. Experiments are performed on liquid samples at Tsub(f)uranium and phosphorus pentoxide vaporize quite selectively up to 1600/sup 0/C with approximately the same rate of vaporization. At higher temperatures only calcic and aluminous compounds remain as stable phases in the residuum.

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

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

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

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

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...

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

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.

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.

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

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

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

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)

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.

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

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

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

Vapor corrosion of aluminum cladding alloys and aluminum-uranium fuel materials in storage environments

International Nuclear Information System (INIS)

Lam, P.; Sindelar, R.L.; Peacock, H.B. Jr.

1997-04-01

An experimental investigation of the effects of vapor environments on the corrosion of aluminum spent nuclear fuel (A1 SNF) has been performed. Aluminum cladding alloys and aluminum-uranium fuel alloys have been exposed to environments of air/water vapor/ionizing radiation and characterized for applications to degradation mode analysis for interim dry and repository storage systems. Models have been developed to allow predictions of the corrosion response under conditions of unlimited corrodant species. Threshold levels of water vapor under which corrosion does not occur have been identified through tests under conditions of limited corrodant species. Coupons of aluminum 1100, 5052, and 6061, the US equivalent of cladding alloys used to manufacture foreign research reactor fuels, and several aluminum-uranium alloys (aluminum-10, 18, and 33 wt% uranium) were exposed to various controlled vapor environments in air within the following ranges of conditions: Temperature -- 80 to 200 C; Relative Humidity -- 0 to 100% using atmospheric condensate water and using added nitric acid to simulate radiolysis effects; and Gamma Radiation -- none and 1.8 x 10 6 R/hr. The results of this work are part of the body of information needed for understanding the degradation of the A1 SNF waste form in a direct disposal system in the federal repository. It will provide the basis for data input to the ongoing performance assessment and criticality safety analyses. Additional testing of uranium-aluminum fuel materials at uranium contents typical of high enriched and low enriched fuels is being initiated to provide the data needed for the development of empirical models

Kinetics of the tungsten hexafluoride-silane reaction for the chemical vapor deposition of tungsten

International Nuclear Information System (INIS)

Gokce, Huseyin.

1991-01-01

In this study, the kinetics of the low-pressure chemical vapor deposition (LPCVD) of tungsten by silane reduction of tungsten hexafluoride on Si(100) surfaces was studied. A single-wafer, cold-wall reactor was sued for the experiments. The SiH 4 /WF 6 ratio was 1.0. The pressure and temperature range were 1-10 torr and 137-385 degree C, respectively. Kinetic data were obtained in the absence of mass-transfer effects. The film thicknesses were measured by gravimetry. Scanning electron microscopy (SEM), Auger electron spectroscopy (AES), x-ray diffraction (XRD), and resistivity measurements were used to analyze the W films. For the horizontal substrate position and 4-minute reaction times, the apparent activation energies were determined to be 0.35 eV/atom for 10 torr, 0.17 eV/atom for 3 torr, and 0.08 eV/atom for 1 torr. Lower temperatures and higher pressures produced porous films, while higher temperatures and lower pressures resulted in continuous films with smoother surfaces. As the Si-W interface, a W(110) preferential orientation was observed. As the W films grew thicker, W orientation switched from (110) to (100). Apparent activation energy seems to change with thickness

Reaction rate constant for uranium in water and water vapor

Energy Technology Data Exchange (ETDEWEB)

TRIMBLE, D.J.

1998-11-09

The literature on uranium oxidation in water and oxygen free water vapor was reviewed. Arrhenius rate equations were developed from the review data. These data and equations will be used as a baseline from which to compare reaction rates measured for K Basin fuel.

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

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

Chemical vapor deposition (CVD) of uranium for alpha spectrometry

International Nuclear Information System (INIS)

Ramirez V, M. L.; Rios M, C.; Ramirez O, J.; Davila R, J. I.; Mireles G, F.

2015-09-01

The uranium determination through radiometric techniques as alpha spectrometry requires for its proper analysis, preparation methods of the source to analyze and procedures for the deposit of this on a surface or substrate. Given the characteristics of alpha particles (small penetration distance and great loss of energy during their journey or its interaction with the matter), is important to ensure that the prepared sources are thin, to avoid problems of self-absorption. The routine methods used for this are the cathodic electro deposition and the direct evaporation, among others. In this paper the use of technique of chemical vapor deposition (CVD) for the preparation of uranium sources is investigated; because by this, is possible to obtain thin films (much thinner than those resulting from electro deposition or evaporation) on a substrate and comprises reacting a precursor with a gas, which in turn serves as a carrier of the reaction products to achieve deposition. Preliminary results of the chemical vapor deposition of uranium are presented, synthesizing and using as precursor molecule the uranyl acetylacetonate, using oxygen as carrier gas for the deposition reaction on a glass substrate. The uranium films obtained were found suitable for alpha spectrometry. The variables taken into account were the precursor sublimation temperatures and deposition temperature, the reaction time and the type and flow of carrier gas. Of the investigated conditions, two depositions with encouraging results that can serve as reference for further work to improve the technique presented here were selected. Alpha spectra obtained for these depositions and the characterization of the representative samples by scanning electron microscopy and X-ray diffraction are also presented. (Author)

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

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)

Theoretical study of adsorption of water vapor on surface of metallic uranium

CERN Document Server

Xiong Bi Tao; Xue Wei Dong; Zhu Zheng He; Jiang Gang; Wang Hong Yan; Gao Tao

2002-01-01

According to the experimental data, there is an intermediate substance that formed in the initial stage of oxidation reaction when water vapor is absorbed onto the metallic uranium. The minimum energy of UOH sub 2 witch C sub 2 subupsilon configuration is obtained in the state of sup 5 A sub 1 by B3LYP method of the density function theory (DFT), which is consistent with that by statics of atoms and molecules reaction (AMRS) and group theory. The results from calculations indicate that the adsorption of water vapor on the metallic uranium is an exothermic reaction and that the adsorbed amount decreases with the elevated temperatures. The adsorptive heat at 1 atm is -205.4747 kJ centre dot mol sup - sup 1 , which indicates a typical chemical adsorption

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

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.

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)

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

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)

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)

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

1 - Description of program or function: HGSYSTEMUF6 is a suite of models designed for use in estimating consequences associated with accidental, atmospheric release of Uranium Hexafluoride (UF 6 ) and its reaction products, namely Hydrogen Fluoride (HF), and other non-reactive contaminants which are either negatively, neutrally, or positively buoyant. It is based on HGSYSTEM Version 3.0 of Shell Research LTD., and contains specific algorithms for the treatment of UF 6 chemistry and thermodynamics. HGSYSTEMUF6 contains algorithms for the treatment of dense gases, dry and wet deposition, effects due to the presence of buildings (canyon and wake), plume lift-off, and the effects of complex terrain. The models components of the suite include (1) AEROPLUME/RK, used to model near-field dispersion from pressurized two-phase jet releases of UF6 and its reaction products, (2) HEGADAS/UF6 for simulating dense, ground based release of UF 6 , (3) PGPLUME for simulation of passive, neutrally buoyant plumes (4) UF6Mixer for modeling warm, potentially reactive, ground-level releases of UF 6 from buildings, and (5) WAKE, used to model elevated and ground-level releases into building wake cavities of non-reactive plumes that are either neutrally or positively buoyant. 2 - Methods: The atmospheric release and transport of UF 6 is a complicated process involving the interaction between dispersion, chemical and thermodynamic processes. This process is characterized by four separate stages (flash, sublimation, chemical reaction entrainment and passive dispersion) in which one or more of these processes dominate. The various models contained in the suite are applicable to one or more of these stages. For example, for modeling reactive, multiphase releases of UF 6 , the AEROPLUME/RK component employs a process-splitting scheme which numerically integrates the differential equations governing dispersion, UF 6 chemistry, and thermodynamics. This algorithm is based on the assumption that

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)

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

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

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

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

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.

Uranium vapor generator: pulsed hollow cathode lamp

International Nuclear Information System (INIS)

Carleer, M.; Gagne, J.; Leblanc, B.; Demers, Y.; Mongeau, B.

1979-01-01

The production of uranium vapors has been studied in the 5 L 0 6 ground state using a pulsed hollow cathode lamp. The evolution of the 238 U ( 5 L 0 6 ) concentration with time has been studied with Xe and Ar as buffer gases. A density of 2.7 x 10 13 atoms cm -3 was obtained with Xe as a buffer gas. In addition, those measurements, obtained from the absorption of a laser beam tuned to the 5758.143 A ( 5 L 0 6 -17,361 7 L 6 ) transition, allowed the determination of the transition probability A=2.1 x 10 5 sec -1 and of the branching ratio BR=0.08 for this transition

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

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)

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)

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.

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

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)

Chemical vapor deposition (CVD) of uranium for alpha spectrometry; Deposicion quimica de vapor (CVD) de uranio para espectrometria alfa

Energy Technology Data Exchange (ETDEWEB)

Ramirez V, M. L.; Rios M, C.; Ramirez O, J.; Davila R, J. I.; Mireles G, F., E-mail: luisalawliet@gmail.com [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Cipres No. 10, Fracc. La Penuela, 98068 Zacatecas (Mexico)

2015-09-15

The uranium determination through radiometric techniques as alpha spectrometry requires for its proper analysis, preparation methods of the source to analyze and procedures for the deposit of this on a surface or substrate. Given the characteristics of alpha particles (small penetration distance and great loss of energy during their journey or its interaction with the matter), is important to ensure that the prepared sources are thin, to avoid problems of self-absorption. The routine methods used for this are the cathodic electro deposition and the direct evaporation, among others. In this paper the use of technique of chemical vapor deposition (CVD) for the preparation of uranium sources is investigated; because by this, is possible to obtain thin films (much thinner than those resulting from electro deposition or evaporation) on a substrate and comprises reacting a precursor with a gas, which in turn serves as a carrier of the reaction products to achieve deposition. Preliminary results of the chemical vapor deposition of uranium are presented, synthesizing and using as precursor molecule the uranyl acetylacetonate, using oxygen as carrier gas for the deposition reaction on a glass substrate. The uranium films obtained were found suitable for alpha spectrometry. The variables taken into account were the precursor sublimation temperatures and deposition temperature, the reaction time and the type and flow of carrier gas. Of the investigated conditions, two depositions with encouraging results that can serve as reference for further work to improve the technique presented here were selected. Alpha spectra obtained for these depositions and the characterization of the representative samples by scanning electron microscopy and X-ray diffraction are also presented. (Author)

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)

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

Vapor pressures and vapor compositions in equilibrium with hypostoichiometric uranium-plutonium dioxide at high temperatures

International Nuclear Information System (INIS)

Green, D.W.; Fink, J.K.; Leibowitz, L.

1982-01-01

Vapor pressures and vapor compositions in equilibrium with a hypostoichiometric uranium-plutonium dioxide condensed phase (U/sub 1-y/Pu/sub y/)O/sub 2-x/, as functions of T, x, and y, have been calculated for 0.0 less than or equal to x less than or equal to 0.1, 0.0 less than or equal to y less than or equal to 0.3, and for the temperature range 2500 less than or equal to T less than or equal to 6000 K. The range of compositions and temperatures was limited to the region of interest to reactor safety analysis. Thermodynamic functions for the condensed phase and for each of the gaseous species were combined with an oxygen potential model to obtain partial pressures of O, O 2 , Pu, PuO, PuO 2 , U, UO, UO 2 , and UO 3 as functions of T, x, and y

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

Thermodynamic functions and vapor pressures of uranium and plutonium oxides at high temperatures

International Nuclear Information System (INIS)

Green, D.W.; Reedy, G.T.; Leibowitz, L.

1977-01-01

The total energy release in a hypothetical reactor accident is sensitive to the total vapor pressure of the fuel. Thermodynamic functions which are accurate at high temperature can be calculated with the methods of statistical mechanics provided that needed spectroscopic data are available. This method of obtaining high-temperature vapor pressures should be greatly superior to the extrapolation of experimental vapor pressure measurements beyond the temperature range studied. Spectroscopic data needed for these calculations are obtained from infrared spectroscopy of matrix-isolated uranium and plutonium oxides. These data allow the assignments of the observed spectra to specific molecular species as well as the calculation of anharmonicities for monoxides, bond angles for dioxides, and molecular geometries for trioxides. These data are then employed, in combination with data on rotational and electronic molecular energy levels, to determine thermodynamic functions that are suitable for the calculation of high-temperature vapor pressures

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)

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

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)

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)

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

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)

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)

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

Method for producing uranium atomic beam source

International Nuclear Information System (INIS)

Krikorian, O.H.

1976-01-01

A method is described for producing a beam of neutral uranium atoms by vaporizing uranium from a compound UM/sub x/ heated to produce U vapor from an M boat or from some other suitable refractory container such as a tungsten boat, where M is a metal whose vapor pressure is negligible compared with that of uranium at the vaporization temperature. The compound, for example, may be the uranium-rhenium compound, URe 2 . An evaporation rate in excess of about 10 times that of conventional uranium beam sources is produced

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)

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.)

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

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

Environmental site description for a Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) production plant at the Paducah Gaseous Diffusion Plant site

International Nuclear Information System (INIS)

Marmer, G.J.; Dunn, C.P.; Moeller, K.L.; Pfingston, J.M.; Policastro, A.J.; Yuen, C.R.; Cleland, J.H.

1991-09-01

Uranium enrichment in the United States has utilized a diffusion process to preferentially enrich the U-235 isotope in the uranium product. The U-AVLIS process is based on electrostatic extraction of photoionized U-235 atoms from an atomic vapor stream created by electron-beam vaporization of uranium metal alloy. The U-235 atoms are ionized when precisely tuned laser light -- of appropriate power, spectral, and temporal characteristics -- illuminates the uranium vapor and selectively photoionizes the U-235 isotope. A programmatic document for use in screening DOE site to locate a U-AVLIS production plant was developed and implemented in two parts. The first part consisted of a series of screening analyses, based on exclusionary and other criteria, that identified a reasonable number of candidate sites. These sites were subjected to a more rigorous and detailed comparative analysis for the purpose of developing a short list of reasonable alternative sites for later environmental examination. This environmental site description (ESD) provides a detailed description of the PGDP site and vicinity suitable for use in an environmental impact statement (EIS). The report is based on existing literature, data collected at the site, and information collected by Argonne National Laboratory (ANL) staff during a site visit. 65 refs., 15 tabs

Environmental site description for a Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) production plant at the Paducah Gaseous Diffusion Plant site

Energy Technology Data Exchange (ETDEWEB)

Marmer, G.J.; Dunn, C.P.; Moeller, K.L.; Pfingston, J.M.; Policastro, A.J.; Yuen, C.R.; Cleland, J.H. (ed.)

1991-09-01

Uranium enrichment in the United States has utilized a diffusion process to preferentially enrich the U-235 isotope in the uranium product. The U-AVLIS process is based on electrostatic extraction of photoionized U-235 atoms from an atomic vapor stream created by electron-beam vaporization of uranium metal alloy. The U-235 atoms are ionized when precisely tuned laser light -- of appropriate power, spectral, and temporal characteristics -- illuminates the uranium vapor and selectively photoionizes the U-235 isotope. A programmatic document for use in screening DOE site to locate a U-AVLIS production plant was developed and implemented in two parts. The first part consisted of a series of screening analyses, based on exclusionary and other criteria, that identified a reasonable number of candidate sites. These sites were subjected to a more rigorous and detailed comparative analysis for the purpose of developing a short list of reasonable alternative sites for later environmental examination. This environmental site description (ESD) provides a detailed description of the PGDP site and vicinity suitable for use in an environmental impact statement (EIS). The report is based on existing literature, data collected at the site, and information collected by Argonne National Laboratory (ANL) staff during a site visit. 65 refs., 15 tabs.

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

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

High-temperature vaporization of thorium-uranium mixed monocarbide (Th1-y, Uy)C

International Nuclear Information System (INIS)

Koyama, Tadafumi; Yamawaki, Michio

1989-01-01

Vaporization thermodynamics of thorium-uranium mixed monocarbide phase (Th 1-y , U y )C was studied by mass spectrometric Knudsen effusion method for the compositions of (Th 0.9 , U 0.1 )C 0.855 , (Th 0.8 , U 0.2 )C 0.973 and (Th 0.6 , U 0.4 )C 0.973 . The partial vapor pressures of Th(g) and U(g) and activities of Th and U of these mixed monocarbides were determined at temperatures ranging from about 2000 to 2200 K. Further, the partial pressures of Th(g) and U(g) and activities of Th and U of the stoichiometric mixed monocarbides (Th 1-y , U y )C 1.00 were evaluated by compensating for the effect of carbon content. The Gibbs energies of formation of stoichiometric (Th 1-y , U y )C 1.00 were also evaluated. (orig.)

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

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.)

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

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

A review of selected aspects of the effect of water vapor on fission gas release from uranium oxycarbide

International Nuclear Information System (INIS)

Myers, B.F.

1994-04-01

A selective review is presented of previous measurements and the analysis of experiments on the effect of water vapor on fission gas release from uranium oxycarbide. Evidence for the time-dependent composition of the uranium oxycarbide fuel; the diffusional release of fission gas; and the initial, rapid and limited release of stored fission gas is discussed. In regard to the initial, rapid release of fission gas, clear restrictions on mechanistic hypotheses can be deduced from the experimental data. However, more fundamental experiments may be required to establish the mechanism of the rapid release

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

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

PROCESS FOR PREPARING URANIUM METAL

Science.gov (United States)

Prescott, C.H. Jr.; Reynolds, F.L.

1959-01-13

A process is presented for producing oxygen-free uranium metal comprising contacting iodine vapor with crude uranium in a reaction zone maintained at 400 to 800 C to produce a vaporous mixture of UI/sub 4/ and iodine. Also disposed within the maction zone is a tungsten filament which is heated to about 1600 C. The UI/sub 4/, upon contacting the hot filament, is decomposed to molten uranium substantially free of oxygen.

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

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

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)

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

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)

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.

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

RECOVERY OF URANIUM FROM ZIRCONIUM-URANIUM NUCLEAR FUELS

Science.gov (United States)

Gens, T.A.

1962-07-10

An improvement was made in a process of recovering uranium from a uranium-zirconium composition which was hydrochlorinated with gsseous hydrogen chloride at a temperature of from 350 to 800 deg C resulting in volatilization of the zirconium, as zirconium tetrachloride, and the formation of a uranium containing nitric acid insoluble residue. The improvement consists of reacting the nitric acid insoluble hydrochlorination residue with gaseous carbon tetrachloride at a temperature in the range 550 to 600 deg C, and thereafter recovering the resulting uranium chloride vapors. (AEC)

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

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

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.

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

Determination of ultratrace amounts of uranium and thorium in aluminium and aluminium alloys by electrothermal vaporization/ICP-MS

International Nuclear Information System (INIS)

Nakamura, Yasushi; Kobayashi, Yoshio; Kakurai, Yousuke

1993-01-01

A method has been developed for determining the 0.01 ng g -1 level of uranium and thorium in aluminium and aluminium alloys by electrothermal vaporization (ETV)/ICP-MS. This method was found to be significantly interfered with any matrices or other elements contained. An ion-exchange technique was therefore applied to separate uranium and thorium from aluminium and other elements. It was known that uranium are adsorbed on an anion-exchange resin and thorium are adsorbed on cation-exchange resin. However, aluminium and copper were eluted with 6 M hydrochloric acid. Dissolve the sample with hydrochloric acid containing copper which was added for analysis of pure aluminium, and oxidize with hydrogen peroxide. Concentration of hydrochloric acid in the solution was adjusted to 6 M, and then passed the solution through the mixed ion-exchange resin column. After the uranium and thorium were eluted with 1 M hydrofluoric acid-0.1 M hydrochloric acid, the solution was evaporated to dryness. It was then dissolved with 1 M hydrochloric acid. Uranium and thorium were analyzed by ETV/ICP-MS using tungsten and molybdenum boats, respectively, since the tungsten boat contained high-level thorium and the molybdenum boat contained uranium. The determination limit of uranium and thorium were 0.003 and 0.005 ng g -1 , respectively. (author)

Dispersion of UO2F2 aerosol and HF vapor in the operating floor during winter ventilation at the Paducah Gaseous Diffusion Plant

International Nuclear Information System (INIS)

Kim, S.H.; Chen, N.C.J.; Taleyarkhan, R.P.; Keith, K.D.; Schmidt, R.W.; Carter, J.C.

1996-01-01

The gaseous diffusion process is currently employed at two plants in the US: the Paducah Gaseous Diffusion Plant and the Portsmouth Gaseous Diffusion Plant. As part of a facility-wide safety evaluation, a postulated design basis accident involving large line-rupture induced releases of uranium hexafluoride (UF 6 ) into the process building of a gaseous diffusion plant (GDP) is evaluated. When UF 6 is released into the atmosphere, it undergoes an exothermic chemical reaction with moisture (H 2 O) in the air to form vaporized hydrogen fluoride (HF) and aerosolized uranyl fluoride (UO 2 F 2 ). These reactants disperse in the process building and transport through the building ventilation system. The ventilation system draws outside air into the process building, distributes it evenly throughout the building, and discharges it to the atmosphere at an elevated temperature. Since air is recirculated from the cell floor area to the operating floor, issues concerning in-building worker safety and evacuation need to be addressed. Therefore, the objective of this study is to evaluate the transport of HF vapor and UO 2 F 2 aerosols throughout the operating floor area following B-line break accident in the cell floor area

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

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

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)

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

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

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)

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.

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

Method and apparatus for separating uranium isotopes

International Nuclear Information System (INIS)

Bernstein, E.R.

1977-01-01

A uranium compound in the solid phase (uranium borohydride four) is subjected to radiation of a first predetermined frequency that excites the uranium-235 isotope-bearing molecules but not the uranium-238 isotope-bearing molecules. The compound is simultaneously subjected to radiation of a second predetermined frequency which causes the excited uranium-235 isotope-bearing molecules to chemically decompose but which does not affect the uranium-238 isotope-bearing molecules. Sufficient heat is then applied to the irradiated compound in the solid phase to vaporize the non-decomposed uranium-238 isotope-bearing molecules but not the decomposed uranium-235 isotope-bearing molecules, thereby physically separating the uranium-235 isotope-bearing molecules from the uranium-238 isotope-bearing molecules. The uranium compound sample in the solid phase is deposited or grown in an elongated tube supported within a dewar vessel having a clear optical path tail section surrounded by a coolant. Two sources of radiation are focused on the uranium compound sample. A heating element is attached to the elongated tube to vaporize the irradiated compound

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

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

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.)

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

Evaporation monitoring and composition control of alloy systems with widely differing vapor pressures

International Nuclear Information System (INIS)

Anklam, T.M.; Berzins, L.V.; Braun, D.G.; Haynam, C.; McClelland, M.A.; Meier, T.

1994-10-01

Lawrence Livermore National Laboratory is developing sensors and controls to improve and extend electron beam materials processing technology to alloy systems with constituents of widely varying vapor pressure. The approach under development involves using tunable lasers to measure the density and composition of the vapor plume. A laser based vaporizer control system for vaporization of a uranium-iron alloy has been previously demonstrated in multi-hundred hour, high rate vaporization experiments at LLNL. This paper reviews the design and performance of the uranium vaporization sensor and control system and discusses the extension of the technology to monitoring of uranium vaporization. Data is presented from an experiment in which titanium wire was fed into a molten niobium pool. Laser data is compared to deposited film composition and film cross sections. Finally, the potential for using this technique for composition control in melting applications is discussed

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

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.)

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

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

Process for recovering uranium

Science.gov (United States)

MacWood, G. E.; Wilder, C. D.; Altman, D.

1959-03-24

A process useful in recovering uranium from deposits on stainless steel liner surfaces of calutrons is presented. The deposit is removed from the stainless steel surface by washing with aqueous nitric acid. The solution obtained containing uranium, chromium, nickel, copper, and iron is treated with an excess of ammonium hydroxide to precipitnte the uranium, iron, and chromium and convert the nickel and copper to soluble ammonio complexions. The precipitated material is removed, dried and treated with carbon tetrachloride at an elevated temperature of about 500 to 600 deg C to form a vapor mixture of UCl/ sub 4/, UCl/sub 5/, FeCl/sub 3/, and CrCl/sub 4/. The UCl/sub 4/ is separated from this vapor mixture by selective fractional condensation at a temperature of about 500 to 400 deg C.

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

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

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

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.

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

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

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.

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

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

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

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)

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)

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).

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.

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)

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...

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

Uranium recovery from AVLIS slag

International Nuclear Information System (INIS)

D'Agostino, A.E.; Mycroft, J.R.; Oliver, A.J.; Schneider, P.G.; Richardson, K.L.

2000-01-01

Uranium metal for the Atomic Vapor Laser Isotope Separation (AVLIS) project was to have been produced by the magnesiothermic reduction of uranium tetrafluoride. The other product from this reaction is a magnesium fluoride slag, which contains fine and entrained natural uranium as metal and oxide. Recovery of the uranium through conventional mill leaching would not give a magnesium residue free of uranium but to achieve more complete uranium recovery requires the destruction of the magnesium fluoride matrix and liberation of the entrapped uranium. Alternate methods of carrying out such treatments and the potential for recovery of other valuable byproducts were examined. Based on the process flowsheets, a number of economic assessments were performed, conclusions were drawn and the preferred processing alternatives were identified. (author)

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

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

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.)

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.…

Thermal plasma reduction of UF6

International Nuclear Information System (INIS)

Fincke, J.R.; Swank, W.D.; Haggard, D.C.

1995-01-01

This paper describes the experimental demonstration of a process for the direct plasma reduction of depleted uranium hexafluoride to uranium metal. The process exploits the large departures from equilibrium that can be achieved in the rapid supersonic expansion of a totally dissociated and partially ionized mixture of UF 6 , Ar, He, and H 2 . The process is based on the rapid condensation of subcooled uranium vapor and the relatively slow rate of back reaction between metallic uranium and HF to F 2 to reform stable fluorides. The high translational velocities and rapid cooling result in an overpopulation of atomic hydrogen which persists throughout the expansion process. Atomic hydrogen shifts the equilibrium composition by inhibiting the reformation of uranium-fluorine compounds. This process has the potential to reduce the cost of reducing UF 6 to uranium metal with the added benefit of being a virtually waste free process. The dry HF produced is a commodity which has industrial value

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.

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

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)

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)

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)

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).

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)

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)

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)

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

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.)

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

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

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

In situ leaching process for recording uranium values

International Nuclear Information System (INIS)

McKnight, W.M.; Timmins, T.H.; Sherry, H.S.

1977-01-01

A method of recovering uranium values from a subterranean deposit comprising: injecting an alkaline carbonate lixiviant into said deposit; flowing said alkaline carbonate lixiviant through said deposit to dissolve said uranium values into said lixiviant; producing said lixiviant and said dissolved uranium values from said deposit; flowing said lixiviant and said dissolved uranium values through an adsorption material to adsorp said uranium values from said lixiviant; eluting said adsorption material with an eluant of ammonium carbonate to desorb said uranium values from said adsorption material into said eluate in a concentration greater than in said lixiviant; heating said eluate and said desorbed uranium values to vaporize off ammonia and carbon dioxide therefrom, thereby causing uranium values to crystallize from the eluate; and recovering said solid uranium values

Uranium metal production by molten salt electrolysis

International Nuclear Information System (INIS)

Takasawa, Yutaka

1999-01-01

Atomic vapor laser isotope separation (AVLIS) is a promising uranium enrichment technology in the next generation. Electrolytic reduction of uranium oxides into uranium metal is proposed for the preparation of uranium metal as a feed material for AVLIS plant. Considering economical performance, continuos process concept and minimizing the amount of radioactive waste, an electrolytic process for producing uranium metal directly from uranium oxides will offer potential advantages over the existing commercial process. Studies of uranium metal by electrolysis in fluoride salts (BaF 2 -LiF-UF 4 (74-11-15 w/o) at 1150-1200degC, using both a laboratory scale apparatus and an engineering scale one, and continuous casting of uranium metal were carried out in order to decide the optimum operating conditions and the design of the industrial electrolytic cells. (author)

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 ...

Salt Separation from Uranium Deposits in Integrated Crucible

Energy Technology Data Exchange (ETDEWEB)

Kwon, S. W.; Park, K. M.; Chang, J. H.; Kim, J. G.; Park, S. B. [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2014-05-15

The solid cathode processing is necessary to separate the salt from the cathode since the uranium deposit in a solid cathode contains electrolyte salt. 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 processsing 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. The adhered salt in the uranium deposits was removed successfully. The salt content in the deposits was below 0.1 wt% after the sequential operation of the liquid salt separation - salt distillation.

Complex defects in the oxidation of uranium

International Nuclear Information System (INIS)

MacCrone, R.K.; Sankaran, S.; Shatynski, S.R.; Colmenares, C.A.

1986-01-01

We are reporting EPR results obtained with uranium powder samples fully oxidized in dry air, water vapor, and air/water vapor mixtures. The results reported previously are confirmed and additional paramagnetic centers, associated with chemisorbed species, have been identified. The temperature dependence of the g-value for these centers from room temperature to 10K is also reported

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)

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

PROCESSES OF CHLORINATION OF URANIUM OXIDES

Science.gov (United States)

Rosenfeld, S.

1958-09-16

An improvement is described in the process fur making UCl/sub 4/ from uranium oxide and carbon tetrachloride. In that process, oxides of uranium are contacted with carbon tetrachloride vapor at an elevated temperature. It has been fuund that the reaction product and yield are improved if the uranlum oxide charge is disposed in flat trays in the reaction zone, to a depth of not more than 1/2 centimeter.

Flow boiling test of GDP replacement coolants

International Nuclear Information System (INIS)

Park, S.H.

1995-01-01

The tests were part of the CFC replacement program to identify and test alternate coolants to replace CFC-114 being used in the uranium enrichment plants at Paducah and Portsmouth. The coolants tested, C 4 F 10 and C 4 F 8 , were selected based on their compatibility with the uranium hexafluoride process gas and how well the boiling temperature and vapor pressure matched that of CFC-114. However, the heat of vaporization of both coolants is lower than that of CFC-114 requiring larger coolant mass flow than CFC-114 to remove the same amount of heat. The vapor pressure of these coolants is higher than CFC-114 within the cascade operational range, and each coolant can be used as a replacement coolant with some limitation at 3,300 hp operation. The results of the CFC-114/C 4 F 10 mixture tests show boiling heat transfer coefficient degraded to a minimum value with about 25% C 4 F 10 weight mixture in CFC-114 and the degree of degradation is about 20% from that of CFC-114 boiling heat transfer coefficient. This report consists of the final reports from Cudo Technologies, Ltd

Status of Uranium Atomic Vapor Laser Isotope Separation Program

International Nuclear Information System (INIS)

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

1993-06-01

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

Physical analytical methods for uranium hexafluoride; Methodes physiques d'analyse de l'hexafluorure d'uranium

Energy Technology Data Exchange (ETDEWEB)

Vandenbussche, G [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

1965-12-15

Various physical methods of analysis currently used or still under investigation such as: sound analysis, vapor pressure measurements, fractional distillation, cryogenics, micro-sublimation, ultra-violet, visible and infra-red absorption spectrophotometry, nuclear magnetic resonance and mass spectrometry are reviewed. For each method, principle and applications are given, and results obtained concerning reproducibility, application limits and rapidity are discussed. (author) [French] On passe en revue les differentes methodes physiques d'analyse utilisees ou en cours d'etude actuellement: par mesure de la vitesse du son, de la pression de vapeur, par distillation fractionnee, cryometrie, microsublimation, spectrometrie d'absorption dans l'ultraviolet, le visible et l'infrarouge, par resonance magnetique nucleaire et par spectrometrie de masse. Pour chaque methode, on donne le principe et son application et on examine les resultats obtenus concernant la reproductibilite, le domaine d'application et la duree des mesures. (auteur)

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)

Environmental site description for a Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) production plant at the Oak Ridge Gaseous Diffusion Plant Site

Energy Technology Data Exchange (ETDEWEB)

1991-09-01

In January 1990, the Secretary of Energy approved a plan for the demonstration and deployment of the Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) technology, with the near-term goal to provide the necessary information to make a deployment decision by November 1992. The U-AVLIS process is based on electrostatic extraction of photoionized U-235 atoms from an atomic vapor stream created by electron-beam vaporization of uranium metal alloy. A programmatic document for use in screening DOE sites to locate the U-AVLIS production plant was developed and implemented in two parts (Wolsko et al. 1991). The first part consisted of a series of screening analyses, based on exclusionary and other criteria, that identified a reasonable number of candidate sites. These sites were then subjected to a more rigorous and detailed comparative analysis for the purpose of developing a short list of reasonable alternative sites for later environmental examination. This environmental site description (ESD) provides a detailed description of the ORGDP site and vicinity suitable for use in an environmental impact statement (EIS). The report is based on existing literature, data collected at the site, and information collected by Argonne National Laboratory (ANL) staff during a site visit. The organization of the ESD is as follows. Topics addressed in Sec. 2 include a general site description and the disciplines of geology, water resources, biotic resources, air resources, noise, cultural resources, land use, socioeconomics, and waste management. Identification of any additional data that would be required for an EIS is presented in Sec. 3. Following the site description and additional data requirements, Sec. 4 provides a short, qualitative assessment of potential environmental issues. 37 refs., 20 figs., 18 tabs.

Environmental site description for a Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) production plant at the Oak Ridge Gaseous Diffusion Plant Site

International Nuclear Information System (INIS)

1991-09-01

In January 1990, the Secretary of Energy approved a plan for the demonstration and deployment of the Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) technology, with the near-term goal to provide the necessary information to make a deployment decision by November 1992. The U-AVLIS process is based on electrostatic extraction of photoionized U-235 atoms from an atomic vapor stream created by electron-beam vaporization of uranium metal alloy. A programmatic document for use in screening DOE sites to locate the U-AVLIS production plant was developed and implemented in two parts (Wolsko et al. 1991). The first part consisted of a series of screening analyses, based on exclusionary and other criteria, that identified a reasonable number of candidate sites. These sites were then subjected to a more rigorous and detailed comparative analysis for the purpose of developing a short list of reasonable alternative sites for later environmental examination. This environmental site description (ESD) provides a detailed description of the ORGDP site and vicinity suitable for use in an environmental impact statement (EIS). The report is based on existing literature, data collected at the site, and information collected by Argonne National Laboratory (ANL) staff during a site visit. The organization of the ESD is as follows. Topics addressed in Sec. 2 include a general site description and the disciplines of geology, water resources, biotic resources, air resources, noise, cultural resources, land use, socioeconomics, and waste management. Identification of any additional data that would be required for an EIS is presented in Sec. 3. Following the site description and additional data requirements, Sec. 4 provides a short, qualitative assessment of potential environmental issues. 37 refs., 20 figs., 18 tabs

Innovative lasers for uranium isotope separation

International Nuclear Information System (INIS)

Brake, M.L.; Gilgenbach, R.M.

1993-07-01

Copper vapor laser have important applications to uranium atomic vapor laser isotope separation (AVLIS). We have investigated two innovative methods of exciting/pumping copper vapor lasers which have the potential to improve the efficiency and scaling of large laser systems used in uranium isotope separation. Experimental research has focused on the laser discharge kinetics of (1) microwave, and (2) electron beam excitation/pumping of large-volume copper vapor lasers. Microwave resonant cavity produced copper vapor plasmas at 2.45 GHz, have been investigated in three separate experimental configurations. The first examined the application of CW (0-500W) power and was found to be an excellent method for producing an atomic copper vapor from copper chloride. The second used a pulsed (5kW, 0.5--5 kHz) signal superimposed on the CW signal to attempt to produce vaporization, dissociation and excitation to the laser states. Enhanced emission of the optical radiation was observed but power densities were found to be too low to achieve lasing. In a third experiment we attempted to increase the applied power by using a high power magnetron to produce 100 kW of pulsed power. Unfortunately, difficulties with the magnetron power supply were encountered leaving inconclusive results. Detailed modeling of the electromagnetics of the system were found to match the diagnostics results well. An electron beam pumped copper vapor system (350 kV, 1.0 kA, 300 ns) was investigated in three separate copper chloride heating systems, external chamber, externally heated chamber and an internally heated chamber. Since atomic copper spectral lines were not observed, it is assumed that a single pulse accelerator is not capable of both dissociating the copper chloride and exciting atomic copper and a repetitively pulsed electron beam generator is needed

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.

Determination of Chlorinated Solvent Sorption by Porous Material-Application to Trichloroethene Vapor on Cement Mortar.

Science.gov (United States)

Musielak, Marion; Brusseau, Mark L; Marcoux, Manuel; Morrison, Candice; Quintard, Michel

2014-08-01

Experiments have been performed to investigate the sorption of trichloroethene (TCE) vapor by concrete material or, more specifically, the cement mortar component. Gas-flow experiments were conducted using columns packed with small pieces of cement mortar obtained from the grinding of typical concrete material. Transport and retardation of TCE at high vapor concentrations (500 mg L -1 ) was compared to that of a non-reactive gas tracer (Sulfur Hexafluoride, SF6). The results show a large magnitude of retardation (retardation factor = 23) and sorption (sorption coefficient = 10.6 cm 3 g -1 ) for TCE, compared to negligible sorption for SF6. This magnitude of sorption obtained with pollutant vapor is much bigger than the one obtained for aqueous-flow experiments conducted for water-saturated systems. The considerable sorption exhibited for TCE under vapor-flow conditions is attributed to some combination of accumulation at the air-water interface and vapor-phase adsorption, both of which are anticipated to be significant for this system given the large surface area associated with the cement mortar. Transport of both SF6 and TCE was simulated successfully with a two-region physical non-equilibrium model, consistent with the dual-medium structure of the crushed cement mortar. This work emphasizes the importance of taking into account sorption phenomena when modeling transport of volatile organic compounds through concrete material, especially in regard to assessing vapor intrusion.

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

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

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.

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

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

Purification method for calcium fluoride containing uranium

International Nuclear Information System (INIS)

Ogami, Takeshi

1998-01-01

Calcium fluoride (CaF 2 ) containing uranium is heated in an electrolytic bath having a cathode and an anode to form a molten salt, and the molten salt is electrolytically reduced to form metal uranium deposited on the surface of the cathode. The calcium fluoride molten salt separated by the deposition of generated metal uranium on the surface of the cathode is solidified by cooling. The solidified calcium fluoride is recovered. When metal uranium is deposited on the surface of the cathode by the electrolytic reduction of the molten salt, impurities such as plutonium and neptunium are also deposited on the surface of the anodes entrained by the metal uranium. Impurities having high vapor pressures such as americium and strontium are evaporated and removed from the molten salts. Then, nuclides such as uranium can thus be separated and recovered, and residual CaF 2 can be recovered in a state easily storable and reutilizable. (T.M.)

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

Lasers and uranium isotope separation

Energy Technology Data Exchange (ETDEWEB)

Gilles, L

1987-12-01

The use of lasers by the electronuclear industry to enrich uranium is discussed, particularly economic aspects. The SILMO and SILVA processes (chosen by France for industrial development) are presented. Criteria which lead to the choice of lasers and to their set-up (architecture of the chain) are described. For electricity - consumption linked to the use of lasers of 40 kWh/STU, a laser uranium enrichment plant with 10 STU/yr capacity requires 50kW of light from copper vapor lasers, i.e., 500 units each having 100W capacity, compared with the 40W units currently marketed.

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.

AEC determines uranium enrichment policy

International Nuclear Information System (INIS)

Anon.

1992-01-01

The Advisory Committee on Uranium Enrichment of the Atomic Energy Commission (AEC) has submitted a report to AEC chairman concerning the promotion of the introduction of advanced material, high performance centrifuges to replace conventional metallic drum centrifuges, and the development of next generation advanced centrifuges. The report also called for the postponement until around 1997 of the decision whether the development should be continued or not on atomic vapor laser isotope separation (AVLIS) and molecular laser isotope separation (MLIS) processes, as well as the virtual freezing of the construction of a chemical process demonstration plant. The report was approved by the AEC chairman in August. The uranium enrichment service market in the world will continue to be characterized by oversupply. The domestic situation of uranium enrichment supply-demand trend, progress of the expansion of Rokkasho enrichment plant, the trend in the development of gas centrifuge process and the basic philosophy of commercializing domestic uranium enrichment are reported. (K.I.)

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

Energetics and dynamics of atomic uranium levels

International Nuclear Information System (INIS)

Miron, E.

1978-01-01

New methods for discovering and identifying new electronic levels of atomic uranium and measuring parameters, such as radiative lifetimes and absorption cross-sections, are described. The uranium atoms are produced within an especially designed induction-heated oven. The uranium vapor is irradiated by nitrogen laser pumped, pulsed dye lasers. The various measurements are accomplished by detection of laser induced fluorescence from selectively excited levels. 138 atomic-uranium odd levels in the region 32260-34900 cm -1 and 16 even levels in the region 49500-49900 cm -1 are reported. Unique J values are presented for 64 levels and partial assignment (two possibilities) for 42 levels. Radiative lifetimes are presented for 134 levels. Absorption cross sections were measured for 12 transitions. Isotope shifts of 17 levels are given. Cross-sections for internal excitation transfer in uranium which are induced by collisions with argon atoms, are presented for 11 levels. (author)

Innovative lasers for uranium isotope separation. [Progress report

Energy Technology Data Exchange (ETDEWEB)

Brake, M.L.; Gilgenbach, R.M.

1991-06-01

Copper vapor lasers have important applications to uranium atomic vapor laser isotope separation (AVLIS). The authors have spent the first two years of their project investigating two innovative methods of exciting/pumping copper vapor lasers which have the potential to improve the efficiency and scaling of large laser systems used in uranium isotope separation. Experimental research has focused on the laser discharge kinetics of (1) microwave, and (2) electron beam excitation/pumping of large-volume copper vapor lasers. During the first year, the experiments have been designed and constructed and initial data has been taken. During the second year these experiments have been diagnosed. Highlights of some of the second year results as well as plans for the future include the following: Microwave resonant cavity produced copper vapor plasmas at 2.45 GHz, have been investigated. A CW (0--500 W) signal heats and vaporizes the copper chloride to provide the atomic copper vapor. A pulsed (5 kW, 0.5--5kHz) signal is added to the incoming CW signal via a hybrid mixer to excite the copper states to the laser levels. An enhancement of the visible radiation has been observed during the pulsed pardon of the signal. Electrical probe measurements have been implemented on the system to verify the results of the electromagnetic model formulated last year. Laser gain measurements have been initiated with the use of a commercial copper vapor laser. Measurements of the spatial profile of the emission are also currently being made. The authors plan to increase the amount of pulsed microwave power to the system by implementing a high power magnetron. A laser cavity will be designed and added to this system.

R and D on laser uranium enrichment

International Nuclear Information System (INIS)

Anon.

1986-01-01

An AEC Advisory Committee on Uranium Enrichment has completed investigations into the actual condition of laser isotope separation. The working group set up for the purpose has issued a report on the series of investigations made on its development and measures for promoting it. The report says that the development of the process in Japan is at a fundamental stage. Noting that further efforts are needed before its future can be predicted, the report proposes a cource of research and development for the immediate future. For the atomic vapor laser isotope separation (AVLIS), government organizations are engaged in data base buildup and conducting basis engineering tests, and Japan Atomic Energy Research Institute will consider the re-enrichment of uranium recovered from reprocessing. Non-governmental unions of researchers will promote the combination of copper-vapor laser and dye laser. For the molecular laser isotope separation (MLIS), the Institute of Physical and Chemical Research will take up studies with the cooperation of the Power Reactor and Nuclear Fuel Development Corporation. In chapters covering the philosophy of laser uranium enrichment technology development, the report deals with its significance, actual conditions and tasks, and goals and measures for its promotion. (Nogami, K.)

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

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.

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)

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)

Scrap uranium recycling via electron beam melting

International Nuclear Information System (INIS)

McKoon, R.

1993-11-01

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

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)

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)

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

Reactions of plutonium dioxide with water and oxygen-hydrogen mixtures: Mechanisms for corrosion of uranium and plutonium

Energy Technology Data Exchange (ETDEWEB)

Haschke, John M.; Allen, Thomas H.; Morales, Luis A.

1999-06-18

Investigation of the interactions of plutonium dioxide with water vapor and with an oxygen-hydrogen mixture show that the oxide is both chemically reactive and catalytically active. Correspondence of the chemical behavior with that for oxidation of uranium in moist air suggests that similar catalytic processes participate in the mechanism of moisture-enhanced corrosion of uranium and plutonium. Evaluation of chemical and kinetic data for corrosion of the metals leads to a comprehensive mechanism for corrosion in dry air, water vapor, and moist air. Results are applied in confirming that the corrosion rate of Pu in water vapor decreases sharply between 100 and 200 degrees C.

Isotopic measurement of uranium using NP-type chelate resin beads

International Nuclear Information System (INIS)

Wu Lanbi; Chen Wenpo; Wang Shijun

1994-08-01

NP-type chelate resin beads is used as a carrier of samples in the isotopic measurements of uranium by mass spectrometry. The results show that its absorption efficiency for uranium can be greater than 50%. It is one order magnitude higher than that strong basic anion resin, however, the ionization efficiencies of both are almost the same. Therefore, the amount of uranium required for isotopic analysis can be reduced one order of magnitude. This method has been used for isotopic analysis of uranium in NP-type chelate resin beads contained 10 -9 ∼ 10 -7 g uranium. For standard sample UTB-500, the external precision of measurements are within +-0.2%, for natural uranium samples are within +- 0.5%. The application of NP-type chelate resin beads in the isotopic measurement of uranium is a new creative achievement. It has been used in the depletion test of uranium-atomic vapor laser isotope separation

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.)

Atomic vapor laser isotope separation

International Nuclear Information System (INIS)

Stern, R.C.; Paisner, J.A.

1985-01-01

Atomic vapor laser isotope separation (AVLIS) is a general and powerful technique. A major present application to the enrichment of uranium for light-water power reactor fuel has been under development for over 10 years. In June 1985 the Department of Energy announced the selection of AVLIS as the technology to meet the nation's future need for the internationally competitive production of uranium separative work. The economic basis for this decision is considered, with an indicated of the constraints placed on the process figures of merit and the process laser system. We then trace an atom through a generic AVLIS separator and give examples of the physical steps encountered, the models used to describe the process physics, the fundamental parameters involved, and the role of diagnostic laser measurements

Uranium reactions with water vapor. Final progress report

International Nuclear Information System (INIS)

Condon, J.B.; Cristy, S.S.; Kirkpatrick, J.R.

1983-01-01

The reaction kinetics and ion microprobe mass analyzer (IMMA) depth-profile data for water-oxygen-uranium reaction is explained in terms of the perfusive-precipitation model. This model is reviewed extensively enough to deal with this interacting, 3-element reaction system. The model, based on simultaneous diffusion and product precipitation, can be applied to several systems in a parameterless fashion. It is applied to the uranium-water reaction in the absence and presence of the oxygen inhibitor. The results of the calculations of the model are compared to the experimental rates and the IMMA depth profiles obtained when 18 O-labeled water is used. The predictions are excellent for the pressure dependence of the rates, the activation energies for both the oxygen-poisoned and oxygen-free reactions, the absolute rates for the oxygen-poisoned case, and the IMMA depth profiles. The prediction of the absolute rate for the oxygen-free case is only within a factor of five due to the approximations made for the thermodynamics of the product layer that fixes the oxygen activity. Comparison of the model to experimental data for other metal-oxidation systems such as iron, silicon, copper, zirconium with oxygen, and thorium with water, is also presented to lend credibility to the modeling technique

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

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.)

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.)

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

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

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

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

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)

Uranium isotope fractionation resulting from UF6 vapor distillation from containers

International Nuclear Information System (INIS)

Hedge, W.D.; Turner, C.M.

1985-01-01

This empirical study for possible isotopic fractionation due to UF 6 vapor distillation from valved containers was performed to determine the effects of repeated vapor sampling. Four different experiments were performed, each of which varied by the method of measuring the isotopic contents and/or by the difference in temperature gradients as follows: The ratio of the parent UF 6 to the desublimed UF 6 collected at liquid nitrogen temperature and homogenized was measured by sampling the containers. The ratio of the parent UF 6 to the desublimed UF 6 collected at liquid nitrogen temperature and homogenized was measured by direct comparison to each other without subsampling. The ratio of the parent UF 6 to the desublimed UF 6 collected at liquid nitrogen and ice-water temperatures and homogenized was measured by indirect comparison to a common UF 6 reference material without subsampling. The ratio of the parent UF 6 to the desublimed UF 6 collected at liquid nitrogen temperature without homogenizing was measured by indirect comparison to a common UF 6 reference. Gas-phase, relative mass spectrometry was used for all isotopic measurements. Results of the study indicate that fractionation does occur. The U-235 isotope becomes more enriched in the parent container as the UF 6 is vaporized from it and desublimed into the receiving cylinder; i.e., the vaporized fraction is enriched in the U-238 isotope. The degree of fractionation indicates that the separation is due to the U-238 isotope of UF 6 having a higher vapor pressure than the U-235 isotope of UF 6 . 3 refs., 4 figs., 4 tabs

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)

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

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

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

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)

Thermodynamic data for uranium fluorides

International Nuclear Information System (INIS)

Leitnaker, J.M.

1983-03-01

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

Multilayer Porous Crucibles for the High Throughput Salt Separation from Uranium Deposits

International Nuclear Information System (INIS)

Kwon, S. W.; Park, K. M.; Kim, J. G.; Kim, I. T.; Seo, B. K.; Moon, J. G.

2013-01-01

Solid cathode processing is necessary to separate the salt from the cathode since the uranium deposit in a solid cathode contains electrolyte salt. A physical separation process, such as a 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 processsing 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 nonvolatile uranium remains behind. It is very important to increase the throughput of the salt separation system owing 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 an electro-refiner. Therefore, a wide evaporation area or high distillation temperature is necessary for the successful salt separation. In this study, it was attempted to enlarge a throughput of the salt distiller with a multilayer porous crucibles for the separation of adhered salt in the uranium deposits generated from the electrorefiner. The feasibility of the porous crucibles was tested by the salt distillation experiments. In this study, the salt distiller with multilayer porous crucibles was proposed and the feasibility of liquid salt separation was examined to increase a throughput. It was found that the effective separation of salt from uranium deposits was possible by the multilayer porous crucibles

Multilayer Porous Crucibles for the High Throughput Salt Separation from Uranium Deposits

Energy Technology Data Exchange (ETDEWEB)

Kwon, S. W.; Park, K. M.; Kim, J. G.; Kim, I. T.; Seo, B. K.; Moon, J. G. [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2013-05-15

Solid cathode processing is necessary to separate the salt from the cathode since the uranium deposit in a solid cathode contains electrolyte salt. A physical separation process, such as a 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 processsing 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 nonvolatile uranium remains behind. It is very important to increase the throughput of the salt separation system owing 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 an electro-refiner. Therefore, a wide evaporation area or high distillation temperature is necessary for the successful salt separation. In this study, it was attempted to enlarge a throughput of the salt distiller with a multilayer porous crucibles for the separation of adhered salt in the uranium deposits generated from the electrorefiner. The feasibility of the porous crucibles was tested by the salt distillation experiments. In this study, the salt distiller with multilayer porous crucibles was proposed and the feasibility of liquid salt separation was examined to increase a throughput. It was found that the effective separation of salt from uranium deposits was possible by the multilayer porous crucibles.

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

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)

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.

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

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

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)

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)

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)

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

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.)

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)

Vapour pressures of uranium and uranium nitride over UN(s)

International Nuclear Information System (INIS)

Venugopal, V.; Kulkarni, S.G.; Subbanna, C.S.; Sood, D.D.

1992-01-01

The vaporization of uranium mononitride is investigated in the temperature range 1757 to 2400 K by Knudsen effusion cell mass spectrometry. The vaporization occurs incongruently by the preferential loss of nitrogen and the formation of U(1) in equilibrium with UN phase. In addition the vapour phase has U(g) and UN(g). The vapour pressure of U(g) and UN(g) are measured and their dependence with temperatures can be represented by: log(p U (Pa))=[(10.59±0.18)-(26857±357)/T(K)] (1757 UN (Pa))=[(12.19±0.57)-(37347±235)/T(K)] (2190 f G 0 (UN, g, T)(kJ/mol)=352.75-0.0494 T(K). The equilibrium constants for the dissociation of UN(s)(K 1 ) and UN(g)(K 2 ) into gaseous elements are given by: log(K 1 )=(13.03±0.18)-(42857±357)/T(K), log(K 2 )=(0.84±0.60)-(5510±427)/T(K). (orig.)

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

Increasing of charge of uranium ion beam in vacuum-arc-type source (MEVVA)

CERN Document Server

Kulevoj, T V; Petrenko, S V; Seleznev, D N; Pershin, V I; Batalin, V A; Kolomiets, A A

2002-01-01

Research efforts with MEVVA type source (Metal Vapor Vacuum Arc) and with its modifications are in progress now in the ITEP. In the course of research one revealed possibility to increase charge state of generated beam of uranium ions. Increase of charge results from propagation of high-current vacuum-arc charge from the source cathode to the extra anode located in increasing axial magnetic field. One obtained uranium ion beam with 150 mA output current 10% of which were contributed by U sup 7 sup + uranium ions

Uranium enrichment

International Nuclear Information System (INIS)

1991-08-01

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

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.

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)

A novel method for the preparation of uranium metal, oxide and carbide via electrolytic amalgamation

International Nuclear Information System (INIS)

Wang, L.C.; Lee, H.C.; Lee, T.S.; Lai, W.C.; Chang, C.T.

1978-01-01

A solid uranium amalgam was prepared electrolytically using a two-compartment cell separated with an ion exchange membrane for the purpose of regulating pH value within a narrowly restricted region of 2 to 3. The mercury cathode was kept at -1.8V vs SCE during electrolysis. The thereby obtained amalgam containing as high as 1.9gm U/ml Hg is easily converted into uranium metal by heating in vacuo above 1300 0 C. Uranium dioxide and uranium monocarbide could be easily obtained at relatively low temperature by reacting the amalgam with water vapor and methane. (author)

A kinetic study of the reaction of water vapor and carbon dioxide on uranium

International Nuclear Information System (INIS)

Santon, J.P.

1964-09-01

The kinetic study of the reaction of water vapour and carbon dioxide with uranium has been performed by thermogravimetric methods at temperatures between 160 and 410 deg G in the first case, 350 and 1050 deg C in the second: Three sorts of uranium specimens were used: uranium powder, thin evaporated films, and small spheres obtained from a plasma furnace. The experimental results led in the case of water vapour, to a linear rate of reaction controlled by diffusion at the lower temperatures, and by a surface reaction at the upper ones. In the case of carbon dioxide, a parabolic law has been found, controlled by diffusional processes. (author) [fr

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

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)

Environmental site description for a Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) production plant at the Portsmouth Gaseous Diffusion Plant site

International Nuclear Information System (INIS)

Marmer, G.J.; Dunn, C.P.; Filley, T.H.; Moeller, K.L.; Pfingston, J.M.; Policastro, A.J.; Cleland, J.H.

1991-09-01

Uranium enrichment in the United States has utilized a diffusion process to preferentially enrich the U-235 isotope in the uranium product. In the 1970s, the US Department of Energy (DOE) began investigating more efficient and cost-effective enrichment technologies. In January 1990, the Secretary of Energy approved a plan for the demonstration and deployment of the Uranium Atomic Vapor Laser isotope Separation (U-AVLIS) technology with the near-term goal to provide the necessary information to make a deployment decision by November 1992. Initial facility operation is anticipated for 1999. A programmatic document for use in screening DOE sites to locate a U-AVLIS production plant was developed and implemented in two parts. The first part consisted of a series of screening analyses, based on exclusionary and other criteria, that identified a reasonable number of candidate sites. The final evaluation, which included sensitivity studies, identified the Oak Ridge Gaseous Diffusion Plant (ORGDP) site, the Paducah Gaseous Diffusion Plant (PGDP) site, and the Portsmouth Gaseous Diffusion Plant (PORTS) site as having significant advantages over the other sites considered. This environmental site description (ESD) provides a detailed description of the PORTS site and vicinity suitable for use in an environmental impact statement (EIS). This report is based on existing literature, data collected at the site, and information collected by Argonne National Laboratory (ANL) staff during site visits. The organization of the ESD is as follows. Topics addressed in Sec. 2 include a general site description and the disciplines of geology, water resources, biotic resources, air resources, noise, cultural resources, land use. Socioeconomics, and waste management. Identification of any additional data that would be required for an EIS is presented in Sec. 3

Environmental site description for a Uranium Atomic Vapor Laser Isotope Separation (U-AVLIS) production plant at the Portsmouth Gaseous Diffusion Plant site

Energy Technology Data Exchange (ETDEWEB)

Marmer, G.J.; Dunn, C.P.; Filley, T.H.; Moeller, K.L.; Pfingston, J.M.; Policastro, A.J.; Cleland, J.H.

1991-09-01

Uranium enrichment in the United States has utilized a diffusion process to preferentially enrich the U-235 isotope in the uranium product. In the 1970s, the US Department of Energy (DOE) began investigating more efficient and cost-effective enrichment technologies. In January 1990, the Secretary of Energy approved a plan for the demonstration and deployment of the Uranium Atomic Vapor Laser isotope Separation (U-AVLIS) technology with the near-term goal to provide the necessary information to make a deployment decision by November 1992. Initial facility operation is anticipated for 1999. A programmatic document for use in screening DOE sites to locate a U-AVLIS production plant was developed and implemented in two parts. The first part consisted of a series of screening analyses, based on exclusionary and other criteria, that identified a reasonable number of candidate sites. The final evaluation, which included sensitivity studies, identified the Oak Ridge Gaseous Diffusion Plant (ORGDP) site, the Paducah Gaseous Diffusion Plant (PGDP) site, and the Portsmouth Gaseous Diffusion Plant (PORTS) site as having significant advantages over the other sites considered. This environmental site description (ESD) provides a detailed description of the PORTS site and vicinity suitable for use in an environmental impact statement (EIS). This report is based on existing literature, data collected at the site, and information collected by Argonne National Laboratory (ANL) staff during site visits. The organization of the ESD is as follows. Topics addressed in Sec. 2 include a general site description and the disciplines of geology, water resources, biotic resources, air resources, noise, cultural resources, land use. Socioeconomics, and waste management. Identification of any additional data that would be required for an EIS is presented in Sec. 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

Uranium enrichment activities: the SILVA program

International Nuclear Information System (INIS)

Guyot, J.; Cazalet, J.; Camarcat, N.; Figuet, J.

1994-01-01

Through its commitment to a nuclear electricity generation policy, France holds today a specific position in the uranium enrichment market thanks to the modern multinational EURODIF gaseous diffusion plant. France has, altogether, a long-term goal in developing SILVA, a laser uranium enrichment process, based on the selective photo-ionization of U-235. After reviewing the fundamentals of SILVA (the laser system with copper vapor lasers and dye lasers and the separator system), a description of the general organization of the R and D program is provided going through basic research, subsystems assessment, production demonstrations and simulations (with the LACAN code), plant design and economics. The general schedule of SILVA is outlined, leading to the possible construction of a commercial plant. 7 figs., 11 refs

Thermodynamic data for uranium fluorides

Energy Technology Data Exchange (ETDEWEB)

Leitnaker, J.M.

1983-03-01

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

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...

Method for the production of uranium chloride salt

Science.gov (United States)

Westphal, Brian R.; Mariani, Robert D.

2013-07-02

A method for the production of UCl.sub.3 salt without the use of hazardous chemicals or multiple apparatuses for synthesis and purification is provided. Uranium metal is combined in a reaction vessel with a metal chloride and a eutectic salt- and heated to a first temperature under vacuum conditions to promote reaction of the uranium metal with the metal chloride for the production of a UCl.sub.3 salt. After the reaction has run substantially to completion, the furnace is heated to a second temperature under vacuum conditions. The second temperature is sufficiently high to selectively vaporize the chloride salts and distill them into a condenser region.

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

Nuclear vapor thermal reactor propulsion technology

International Nuclear Information System (INIS)

Maya, I.; Diaz, N.J.; Dugan, E.T.; Watanabe, Y.; McClanahan, J.A.; Wen-Hsiung Tu; Carman, R.L.

1993-01-01

The conceptual design of a nuclear rocket based on the vapor core reactor is presented. The Nuclear Vapor Thermal Rocket (NVTR) offers the potential for a specific impulse of 1000 to 1200 s at thrust-to-weight ratios of 1 to 2. The design is based on NERVA geometry and systems with the solid fuel replaced by uranium tetrafluoride (UF 4 ) vapor. The closed-loop core does not rely on hydrodynamic confinement of the fuel. The hydrogen propellant is separated from the UF 4 fuel gas by graphite structure. The hydrogen is maintained at high pressure (∼100 atm), and exits the core at 3,100 K to 3,500 K. Zirconium carbide and hafnium carbide coatings are used to protect the hot graphite from the hydrogen. The core is surrounded by beryllium oxide reflector. The nuclear reactor core has been integrated into a 75 klb engine design using an expander cycle and dual turbopumps. The NVTR offers the potential for an incremental technology development pathway to high performance gas core reactors. Since the fuel is readily available, it also offers advantages in the initial cost of development, as it will not require major expenditures for fuel development

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

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

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.

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)

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

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

International Nuclear Information System (INIS)

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

1994-01-01

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

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

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.)

Kinetics of laser pulse vaporization of uranium dioxide by mass spectrometry

Energy Technology Data Exchange (ETDEWEB)

Tsai, C.

1981-11-01

Safety analyses of nuclear reactors require knowledge of the evaporation behavior of UO/sub 2/ at temperatures well above the melting point of 3140 K. In this study, rapid transient heating of a small spot on a UO/sub 2/ specimen was accomplished by a laser pulse, which generates a surface temperature excursion. This in turn vaporizes the target surface and the gas expands into vacuum. The surface temperature transient was monitored by a fast-response automatic optical pyrometer. The maximum surface temperatures investigated range from approx. 3700 K to approx. 4300 K. A computer program was developed to simulate the laser heating process and calculate the surface temperature evolution. The effect of the uncertainties of the high temperature material properties on the calculation was included in a sensitivity study for UO/sub 2/ vaporization. The measured surface temperatures were in satisfactory agreements.

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

Uranium and sulphate values from carbonate leach process

International Nuclear Information System (INIS)

Berger, B.

1983-01-01

The process concerns the recovery of uraniferous and sulphur values from liquor resulting from the attack of sulphur containing uraniferous ores by an alkaline solution of sodium carbonate and/or bicarbonate. Ammonia is introduced into the liquor to convert any HCO 3 - to CO 3 2- . The neutralised liquor from this step is then contacted with an anion exchange resin to fix the uranium and sulphate ions, leaving a liquor containing ammonia, sodium carbonate and/or bicarbonate in solution. Uranium and sulphate ions are eluted with an ammonia carbonate and/or bicarbonate solution to yield a solution of ammonium uranyl carbonate complex and ammonium sulphate. The solution is subjected to thermal treatment until a suspension of precipitated ammonium uranate and/or diuranate is obtained in a solution of the ammonium sulphate. Carbon dioxide, ammonia and water vapor are driven off. The precipitated ammonium uranate and/or diuranate is then separated from the solution of ammonium sulphate and the precipitate is calcined to yield uranium trioxide and ammonia

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)

Uranium Oxide Rate Summary for the Spent Nuclear Fuel (SNF) Project (OCRWM)

Energy Technology Data Exchange (ETDEWEB)

PAJUNEN, A.L.

2000-09-20

The purpose of this document is to summarize the uranium oxidation reaction rate information developed by the Hanford Spent Nuclear Fuel (SNF) Project and describe the basis for selecting reaction rate correlations used in system design. The selection basis considers the conditions of practical interest to the fuel removal processes and the reaction rate application during design studies. Since the reaction rate correlations are potentially used over a range of conditions, depending of the type of evaluation being performed, a method for transitioning between oxidation reactions is also documented. The document scope is limited to uranium oxidation reactions of primary interest to the SNF Project processes. The reactions influencing fuel removal processes, and supporting accident analyses, are: uranium-water vapor, uranium-liquid water, uranium-moist air, and uranium-dry air. The correlation selection basis will consider input from all available sources that indicate the oxidation rate of uranium fuel, including the literature data, confirmatory experimental studies, and fuel element observations. Trimble (2000) summarizes literature data and the results of laboratory scale experimental studies. This document combines the information in Trimble (2000) with larger scale reaction observations to describe uranium oxidation rate correlations applicable to conditions of interest to the SNF Project.

Uranium Oxide Rate Summary for the Spent Nuclear Fuel (SNF) Project (OCRWM)

International Nuclear Information System (INIS)

PAJUNEN, A.L.

2000-01-01

The purpose of this document is to summarize the uranium oxidation reaction rate information developed by the Hanford Spent Nuclear Fuel (SNF) Project and describe the basis for selecting reaction rate correlations used in system design. The selection basis considers the conditions of practical interest to the fuel removal processes and the reaction rate application during design studies. Since the reaction rate correlations are potentially used over a range of conditions, depending of the type of evaluation being performed, a method for transitioning between oxidation reactions is also documented. The document scope is limited to uranium oxidation reactions of primary interest to the SNF Project processes. The reactions influencing fuel removal processes, and supporting accident analyses, are: uranium-water vapor, uranium-liquid water, uranium-moist air, and uranium-dry air. The correlation selection basis will consider input from all available sources that indicate the oxidation rate of uranium fuel, including the literature data, confirmatory experimental studies, and fuel element observations. Trimble (2000) summarizes literature data and the results of laboratory scale experimental studies. This document combines the information in Trimble (2000) with larger scale reaction observations to describe uranium oxidation rate correlations applicable to conditions of interest to the SNF Project

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)

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.)

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.)

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

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.

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

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)

Isotopic analysis of uranium by thermoionic mass spectrometry

International Nuclear Information System (INIS)

Moraes, N.M.P. de.

1979-01-01

Uranium isotopic ratio measurements by thermoionic spectrometry are presented. Emphasis is given upon the investigation of the parameters that directly affect the precision and accuracy of the results. Optimized procedures, namely, chemical processing, sample loading on the filaments, vaporization, ionization and measurements of ionic currents, are established. Adequate statistical analysis of the data for the calculation of the internal and external variances and mean standard deviation are presented. These procedures are applied to natural and NBS isotopic standard uranium samples. The results obtained agree with the certified values within specified limits. 235 U/ 238 U isotopic ratios values determined for NBS-U500, and a series of standard samples with variable isotopic compositon, are used to calculate mass discrimination factor [pt

Improved method for removing metal vapor from gas streams

International Nuclear Information System (INIS)

Ahluwalia, R.K.; Im, K.H.

1994-01-01

This invention relates to a process for gas cleanup to remove one or more metallic contaminants present as vapor. More particularly, the invention relates to a gas cleanup process using mass transfer to control the saturation levels such that essentially no particulates are formed, and the vapor condenses on the gas passage surfaces. It addresses the need to cleanup an inert gas contaminated with cadmium which may escape from the electrochemical processing of Integral Fast Reactor (IFR) fuel in a hot cell. The IFR is a complete, self-contained, sodium-cooled, pool-type fast reactor fueled with a metallic alloy of uranium, plutonium and zirconium, and is equipped with a close-coupled fuel cycle. Tests with a model have shown that removal of cadmium from argon gas is in the order of 99.99%. The invention could also apply to the industrial cleanup of air or other gases contaminated with zinc, lead, or mercury. In addition, the invention has application in the cleanup of other gas systems contaminated with metal vapors which may be toxic or unhealthy

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

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)

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)

Separation and recovery of uranium ore by chlorinating, chelate resin and molten salt treatment

International Nuclear Information System (INIS)

Taki, Tomohiro

2000-12-01

Three fundamental researches of separation and recovery of uranium from uranium ore are reported in this paper. Three methods used the chloride pyrometallurgy, sodium containing molten salts and chelate resin. When uranium ore is mixed with activated carbon and reacted for one hour under the mixed gas of chlorine and oxygen at 950 C, more than 90% uranium volatilized and vaporization of aluminum, silicone and phosphorus were controlled. The best activated carbon was brown coal because it was able to control the large range of oxygen concentration. By blowing oxygen into the molten sodium hydroxide, the elution rate of uranium attained to about 95% and a few percent of uranium was remained in the residue. On the uranium ore of unconformity-related uranium deposits, a separation method of uranium, molybdenum, nickel and phosphorus from the sulfuric acid elusion solution with U, Ni, As, Mo, Fe and Al was developed. Methylene phosphonic acid type chelate resin (RCSP) adsorbed Mo and U, and then 100 % Mo was eluted by sodium acetate solution and about 100% U by sodium carbonate solution. Ni and As in the passing solution were recovered by imino-diacetic acid type chelate resin and iron hydroxide, respectively. (S.Y.)

Recent developments in the United States uranium enrichment enterprise

International Nuclear Information System (INIS)

Longenecker, J.R.

1987-01-01

In the near term, DOE is reducing production costs at the gaseous diffusion plants (GDPs), and we've made significant progress already. GDP production costs are expected to decline even further in the near future. DOE is also negotiating new power contracts for the GDPs. The new power contracts, capital improvements, and the use of more unfirm power should reduce our GDP average cost of production to about $60/SWU in the 1990s. Significant technical progress on the Atomic Vapor Laser Isotope Separation (AVLIS) advanced enrichment technology has been made recently. The highlight has been a series of half-scale integrated enrichment experiments using the Laser Demonstration Facility and the Mars separator. We are also ready to initiate testing in the full-scale Separator Demonstration Facility, including a 100 hour run that will vaporize over 5 tons of uranium. DOE is developing plans to restructure the enterprise into a more businesslike entity. The key objective in 1987 is to work with Congress to advance the restructuring of the U.S. uranium enrichment enterprise, to assure its long term competitiveness. We hope to establish in law the charter, objectives, and goals for the restructured enterprise. DOE expects that the world price for enrichment services will continue to decrease in the future. There should be sufficient excess enrichment capacity in the future to assure that competition will be keen. Such a healthy, competitive, world enrichment market will be beneficial to both suppliers and consumers of uranium enrichment services. (J.P.N.)

Study of ion plating parameters, coating structure, and corrosion protection for aluminum coatings on uranium

International Nuclear Information System (INIS)

Egert, C.M.; Scott, D.G.

1987-01-01

A study of ion-plating parameters (primarily deposition rate and substrate bias voltage), coating structure, and the corrosion protection provided by aluminum coatings on uranium is presented. Ion plating at low temperatures yields a variety of aluminum coating structures on uranium. For example, aluminum coatings produced at high deposition rates and low substrate bias voltages are columnar with voids between columns, as expected for high-rate vapor deposition at low temperatures. On the other hand, low deposition rate and high bias voltage produce a modified coating with a dense, noncolumnar structure. These results are not in agreement with other studies that have found no relationship between deposition rate and coating structure in ion plating. This discrepancy is probably due to the high deposition rates used in these studies. An accelerated, water vapor corrosion test indicates that the columnar aluminum coatings provide some corrosion protection despite their porous nature; however, the dense noncolumnar coatings provide significantly greater protection. These results indicate that ion-plated aluminum coatings produced at low deposition rates and high substrate bias voltages creates dense coating structures that are most effective in protecting uranium from corrosion

Uranium- and thorium-bearing pegmatites of the United States

International Nuclear Information System (INIS)

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

1980-04-01

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

Uranium- and thorium-bearing pegmatites of the United States

Energy Technology Data Exchange (ETDEWEB)

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

1980-04-01

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

The red atom. The help of german scientists to USSR between 1945-1961

International Nuclear Information System (INIS)

Andurand, R.

2009-01-01

In this issue is tackled the cooperation between German and Russian scientists in nuclear energy from 1945 to 1961 and especially about the uranium enrichment by gaseous diffusion of uranium hexafluoride in cascade. The problems they encountered and their solutions are related until the explosion of the first Russian atomic bomb even if it was not a bomb with enriched uranium but with plutonium got in a nuclear reactor. (N.C.)

Using laser absorption spectroscopy to monitor composition and physical properties of metal vapors

International Nuclear Information System (INIS)

Berzins, L.V.

1993-01-01

The Atomic Vapor Laser Isotope Separation (AVLIS) program has been using laser absorption spectroscopy to monitor vapor densities for over 15 years. Laser absorption spectroscopy has proven itself to be an accurate and reliable method to monitor both density and composition. During this time the diagnostic has moved from a research tool toward a robust component of a process control system. The hardware used for this diagnostic is discussed elsewhere at this symposium. This paper describes how the laser absorption spectroscopy diagnostic is used as a component of a process control system as well as supplying detailed measurements on vapor densities, composition, flow velocity, internal and kinetic temperatures, and constituent distributions. Examples will be drawn from the uranium AVLIS program. In addition potential applications such as composition control in the production of metal matrix composites or aircraft alloys will be discussed

UO{sub 2} surface oxidation by mixtures of water vapor and hydrogen as a function of temperature

Energy Technology Data Exchange (ETDEWEB)

Espriu-Gascon, A., E-mail: alexandra.espriu@upc.edu [Department of Chemical Engineering, Universitat Politècnica Catalunya-Barcelona Tech, Diagonal 647, E-08028 Barcelona (Spain); Llorca, J.; Domínguez, M. [Institut de Tècniques Energètiques (INTE), Universitat Politècnica Catalunya-Barcelona Tech, Diagonal 647, E-08028 Barcelona (Spain); Centre for Research in NanoEngineering (CRNE), Universitat Politècnica Catalunya-Barcelona Tech, Diagonal 647, E-08028 Barcelona (Spain); Giménez, J.; Casas, I. [Department of Chemical Engineering, Universitat Politècnica Catalunya-Barcelona Tech, Diagonal 647, E-08028 Barcelona (Spain); Pablo, J. de [Department of Chemical Engineering, Universitat Politècnica Catalunya-Barcelona Tech, Diagonal 647, E-08028 Barcelona (Spain); Fundació CTM Centre Tecnològic, Plaça de la Ciència 2, E-08243 Manresa (Spain)

2015-12-15

In the present work, X-Ray Photoelectron Spectroscopy (XPS) was used to study the effect of water vapor on the UO{sub 2} surface as a function of temperature. The experiments were performed in situ inside a high pressure chamber attached to the XPS instrument. UO{sub 2} samples were put in contact with either hydrogen or argon streams, saturated with water at room temperature, and the sample surface evolution was analyzed by XPS. In the case of the water vapor/argon experiments, one experiment at 350 °C was performed and, in the case of the water vapor/hydrogen experiments, the temperatures used inside the reactor were 60, 120, 200 and 350 °C. On one hand, in presence of argon, the results obtained showed that the water vapor in the argon stream oxidized 93% of the U(IV) in the sample surface. On the other hand, the degree of UO{sub 2} surface oxidation showed a different dependence on the temperature in the experiments performed in the presence of hydrogen: the maximum surface oxidation occurred at 120 °C, where 65.4% of U(IV) in the sample surface was oxidized, while at higher temperatures, the surface oxidation decreased. This observation is attributed to the increase of hydrogen reducing effect when temperature increases which prevents part of the oxidation of the UO{sub 2} surface by the water vapor. - Highlights: • UO{sub 2} surface has been oxidized by water vapor in an argon stream at 350 °C. • H{sub 2} reduced more uranium oxidation produced by water at 350 °C when compared to Ar. • In H{sub 2} presence, the uranium oxidation produced by water depends on the temperature.

NF ISO 7097-1. Nuclear fuel technology - Uranium dosimetry in solutions, in uranium hexafluoride and in solids - Part 1: reduction with iron (II) / oxidation with potassium bi-chromate / titration method

International Nuclear Information System (INIS)

2002-04-01

This standard document describes the mode of operation of three different methods for the quantitative dosimetry of uranium in solutions, in UF 6 and in solids: reduction by iron (II), oxidation by potassium bi-chromate and titration. (J.S.)

Galvanic cell for processing of used nuclear fuel

Science.gov (United States)

Garcia-Diaz, Brenda L.; Martinez-Rodriguez, Michael J.; Gray, Joshua R.; Olson, Luke C.

2017-02-07

A galvanic cell and methods of using the galvanic cell is described for the recovery of uranium from used nuclear fuel according to an electrofluorination process. The galvanic cell requires no input energy and can utilize relatively benign gaseous fluorinating agents. Uranium can be recovered from used nuclear fuel in the form of gaseous uranium compound such as uranium hexafluoride, which can then be converted to metallic uranium or UO.sub.2 and processed according to known methodology to form a useful product, e.g., fuel pellets for use in a commercial energy production system.

Electrochemical fluorination for processing of used nuclear fuel

Science.gov (United States)

Garcia-Diaz, Brenda L.; Martinez-Rodriguez, Michael J.; Gray, Joshua R.; Olson, Luke C.

2016-07-05

A galvanic cell and methods of using the galvanic cell is described for the recovery of uranium from used nuclear fuel according to an electrofluorination process. The galvanic cell requires no input energy and can utilize relatively benign gaseous fluorinating agents. Uranium can be recovered from used nuclear fuel in the form of gaseous uranium compound such as uranium hexafluoride, which can then be converted to metallic uranium or UO.sub.2 and processed according to known methodology to form a useful product, e.g., fuel pellets for use in a commercial energy production system.

Uranium hexafluoride container design no. 0236

International Nuclear Information System (INIS)

1976-02-01

The specification covers the construction of the mild steel container complete with cover, sealing ring, sealing plug and with mild steel skirt and lifting lug welded on as shown. It specifies in detail only those factors essential to the maintenance of interchangeability on the plant between containers supplied by different manufacturers. (U.K.)

Reactions of uranium hexafluoride photolysis products

Science.gov (United States)

Lyman, John L.; Laguna, Glenn; Greiner, N. R.

1985-01-01

This paper confirms that the ultraviolet photolysis reactions of UF6 in the B band spectral region is simple bond cleavage to UF5 and F. The photolysis products may either recombine to UF6 or the UF5 may dimerize, and ultimately polymerize, to solid UF5 particles. We use four methods to set an upper limit for the rate constant for recombination of krUF6 and UF5 after laser photolysis of the UF6 gas sample.

Industrias Nucleares do Brasil in the context of the Brazilian nuclear program

International Nuclear Information System (INIS)

1996-10-01

The activities carried out by Industrias Nucleares Brasileiras (INB) related to the nuclear fuel cycle are described. These activities comprise presently uranium prospecting and processing and fuel elements assembly.Starting in 1997,INB will also perform the reconversion of enriched uranium hexafluoride and the fabrication of fuel pellets.Furthermore, INB produces as well rare earth oxides

Correlation of radioactive waste treatment costs and the environmental impact of waste effluents in the nuclear fuel cycle: conversion of recycle uranium to UF6

International Nuclear Information System (INIS)

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

1977-04-01

A cost/benefit study was made to determine the cost and effectiveness of various radioactive waste (radwaste) treatment systems for decreasing the amount of radioactive materials released from a model recycle uranium conversion and uranium hexafluoride (UF 6 ) production plant and to determine the radiological impact (dose commitment) of the released radioactive materials on the environment. This study is designed to assist the US NRC in defining the term ''as low as reasonably achievable'' as it applies to these nuclear facilities. The base case model plant is representative of a licensable UF 6 production plant and has an annual capacity of 1500 metric tons of uranium. Additional radwaste treatment systems are added 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 cost for the added waste treatment operations and the corresponding dose commitments is 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. The methodology used in estimating the costs is presented

Health and environmental impact of depleted uranium

International Nuclear Information System (INIS)

Furitsu, Katsumi

2010-01-01

Depleted Uranium (DU) is 'nuclear waste' produced from the enrichment process and is mostly made up of 238 U and is depleted in the fissionable isotope 235 U compared to natural uranium (NU). Depleted uranium has about 60% of the radioactivity of natural uranium. Depleted uranium and natural uranium are identical in terms of the chemical toxicity. Uranium's high density gives depleted uranium shells increased range and penetrative power. This density, combined with uranium's pyrophoric nature, results in a high-energy kinetic weapon that can punch and burn through armour plating. Striking a hard target, depleted uranium munitions create extremely high temperatures. The uranium immediately burns and vaporizes into an aerosol, which is easily diffused in the environment. People can inhale the micro-particles of uranium oxide in an aerosol and absorb them mainly from lung. Depleted uranium has both aspects of radiological toxicity and chemical toxicity. The possible synergistic effect of both kinds of toxicities is also pointed out. Animal and cellular studies have been reported the carcinogenic, neurotoxic, immuno-toxic and some other effects of depleted uranium including the damage on reproductive system and foetus. In addition, the health effects of micro/ nano-particles, similar in size of depleted uranium aerosols produced by uranium weapons, have been reported. Aerosolized DU dust can easily spread over the battlefield spreading over civilian areas, sometimes even crossing international borders. Therefore, not only the military personnel but also the civilians can be exposed. The contamination continues after the cessation of hostilities. Taking these aspects into account, DU weapon is illegal under international humanitarian laws and is considered as one of the inhumane weapons of 'indiscriminate destruction'. The international society is now discussing the prohibition of DU weapons based on 'precautionary principle'. The 1991 Gulf War is reportedly the first

Metal-free reduction of the greenhouse gas sulfur hexafluoride, formation of SF5 containing ion pairs and the application in fluorinations

KAUST Repository

Rueping, Magnus; Nikolaienko, Pavlo; Lebedev, Yury; Adams, Alina

2017-01-01

A protocol for the fast and selective two-electron reduction of the potent greenhouse gas sulfur hexafluoride (SF6) by organic electron donors at ambient temperature has been developed. The reaction yields solid ion pairs consisting of donor

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)

Study on the surface reaction of uranium metal in hydrogen atmosphere with XPS

International Nuclear Information System (INIS)

Wang Xiaolin; Fu Yibei; Xie Renshou; Zuo Changming; Zhao Chunpei; Chen Hong

1998-01-01

The surface reactions of uranium metal in hydrogen atmosphere at 25 degree C and 200 degree C and effects of temperature and carbon monoxide to the hydriding reaction have been studied by X-ray photoelectron spectroscopy (XPS). The reaction between H 2 and uranium metal at 25 degree C leads to the further oxidation of surface layer of metal due to traces of water vapor. At 200 degree C, it may lead to the hydriding reaction of uranium and the hydriding increases with increasing exposure to H 2 in the initial stages. The U4f 7/2 binding energy of UH 3 has been found to be 378.6 eV. Investigation indicates carbon monoxide inhibits both the hydriding reaction and oxidation on the condition of H 2 -CO atmosphere

Distillation modeling for a uranium refining process

International Nuclear Information System (INIS)

Westphal, B.R.

1996-01-01

As part of the spent fuel treatment program at Argonne National Laboratory, a vacuum distillation process is being employed for the recovery of uranium following an electrorefining process. Distillation of a salt electrolyte, containing a eutectic mixture of lithium and potassium chlorides, from uranium is achieved by a simple batch operation and is termed open-quotes cathode processingclose quotes. The incremental distillation of electrolyte salt will be modeled by an equilibrium expression and on a molecular basis since the operation is conducted under moderate vacuum conditions. As processing continues, the two models will be compared and analyzed for correlation with actual operating results. Possible factors that may contribute to aberrations from the models include impurities at the vapor-liquid boundary, distillate reflux, anomalous pressure gradients, and mass transport phenomena at the evaporating surface. Ultimately, the purpose of either process model is to enable the parametric optimization of the process

Distillation modeling for a uranium refining process

Energy Technology Data Exchange (ETDEWEB)

Westphal, B.R.

1996-03-01

As part of the spent fuel treatment program at Argonne National Laboratory, a vacuum distillation process is being employed for the recovery of uranium following an electrorefining process. Distillation of a salt electrolyte, containing a eutectic mixture of lithium and potassium chlorides, from uranium is achieved by a simple batch operation and is termed {open_quotes}cathode processing{close_quotes}. The incremental distillation of electrolyte salt will be modeled by an equilibrium expression and on a molecular basis since the operation is conducted under moderate vacuum conditions. As processing continues, the two models will be compared and analyzed for correlation with actual operating results. Possible factors that may contribute to aberrations from the models include impurities at the vapor-liquid boundary, distillate reflux, anomalous pressure gradients, and mass transport phenomena at the evaporating surface. Ultimately, the purpose of either process model is to enable the parametric optimization of the process.

Scoping study to expedite development of a field deployable and portable instrument for UF6 enrichment assay

OpenAIRE

Chan, CYG; Valentine, JD; Russo, RE

2017-01-01

The primary objective of the present study is to identity the most promising, viable technologies that are likely to culminate in an expedited development of the next-generation, field-deployable instrument for providing rapid, accurate, and precise enrichment assay of uranium hexafluoride (UF6). UF6 is typically involved, and is arguably the most important uranium compound, in uranium enrichment processes. As the first line of defense against proliferation, accurate analytical techniques t...

Implementation of the environmental management system in nuclear fuel cycle. A case study of the USEXA - CTMSP

International Nuclear Information System (INIS)

Mattiolo, Sandra Regina; Aquino, Afonso Rodrigues de

2009-01-01

CTMSP is the institution where the Brazilian Nuclear Navy Program is developed. The objective of this program is to dominate the technology, industrial and operational processes in nuclear facilities, applied to navy propulsion. In the nuclear fuel cycle, the most complex technological stage is the Uranium Enrichment, that is, a higher concentration of Uranium isotope 235, allowing its utilization as a fuel element of the nuclear reactor. The USEXA - Unit of Production of Uranium Hexafluoride will develop the following stages of the project cycle: material reception and storage, washing drum, production of uranyl nitrate, production of uranium trioxide, production of uranium tetrafluoride; production of fluorine; production of uranium hexafluoride; recoveries of uranium; effluent and waste treatment; and storage of chemical products. This paper presents the advantages and the importance of the Environmental Management System - EMS application, in accordance with ISO 14001: 2004 standard, in Nuclear Public Units, in implementation stages. The incentives are sent to the responsible sectors with questions on the environment, to be answered by the workers affected. An EMS brings any company (public or private) benefits resulting from its implementation, decreasing expenses, enhancing the environment and expanding human resources capability. The paper also shows a new approach of the Environmental Management Implementation: an outside and inside view, with personal motivation as the main tool in human resources. (author)

Pena Blanca uranium deposits and ash-flow tuffs relationship

International Nuclear Information System (INIS)

Magonthier, M.

1987-01-01

The Pena Blanca uranium deposits (Chihuahua, Mexico) are associated with a Tertiary sequence of ash-flow tuffs. Stratigraphic control is dominant and uranium mineralization occurs in stratiform and fracture-controlled deposits within 44 My-old units: Nopal Rhyolite and Escuadra Rhyolite. These units consist of highly vapor-phase crystallized ash-flow tuffs. They contain sanidine, quartz and granophyric phenocrysts, and minor ferromagnesian silicates. Nopal and Escuadra units are high-silica alkali-rich rhyolites that have a primary potassic character. The trace-element chemistry shows high concentrations in U-Th-Rb-Cs and low contents in Ba-Sr-Eu. These chemical properties imply a genetic relationship between deposits and host-units. The petrochemical study show that the Nopal Rhyolite and Escuadra Rhyolite are the source of U and of hydrothermal solutions [fr

Ionization and excitation of uranium in a hollow-cathode lamp

International Nuclear Information System (INIS)

Gagne, J.M.; Pianarosa, P.; Larin, G.; Saint-Dizier, J.P.; Bouchard, P.

1981-01-01

The influence of different carrier gases (Ne,Ar,Kr,Xe) their pressure, and discharge current on the excitation and ionization of uranium atoms in a vapor generator of hollow-cathode design has been investigated by monitoring emission line intensities. From our measurements of line intensities as a function of the carrier gas we obtain an indication of the role of Penning collisions on the excitation of radiative levels in U II

Mobile vapor recovery and vapor scavenging unit

International Nuclear Information System (INIS)

Stokes, C.A.; Steppe, D.E.

1991-01-01

This patent describes a mobile anti- pollution apparatus, for the recovery of hydrocarbon emissions. It comprises a mobile platform upon which is mounted a vapor recovery unit for recovering vapors including light hydrocarbons, the vapor recovery unit having an inlet and an outlet end, the inlet end adapted for coupling to an external source of hydrocarbon vapor emissions to recover a portion of the vapors including light hydrocarbons emitted therefrom, and the outlet end adapted for connection to a means for conveying unrecovered vapors to a vapor scavenging unit, the vapor scavenging unit comprising an internal combustion engine adapted for utilizing light hydrocarbon in the unrecovered vapors exiting from the vapor recovery unit as supplemental fuel

Thermodynamic properties of uranium--mercury system

International Nuclear Information System (INIS)

Lee, T.S.

1979-01-01

The EMF values in the fused salt cells of the type U(α)/KCl--LiCl--BaCl 2 eutectic, UCl 3 /U--Hg alloy, for the different two-phase alloys in the uranium--mercury system have been measured and the thermodynamic properties of this system have been calculated. These calculated values are in good agreement with values based on mercury vapor pressure measurements made by previous investigators. The inconsistency of the thermodynamic properties with the phase diagram determined by Frost are also confirmed. A tentative phase diagram based on the thermodynamic properties measured in this work was constructed

Industrias Nucleares do Brasil in the context of the Brazilian nuclear program; A INB no contexto do programa nuclear brasileiro

Energy Technology Data Exchange (ETDEWEB)

NONE

1996-10-01

The activities carried out by Industrias Nucleares Brasileiras (INB) related to the nuclear fuel cycle are described. These activities comprise presently uranium prospecting and processing and fuel elements assembly.Starting in 1997,INB will also perform the reconversion of enriched uranium hexafluoride and the fabrication of fuel pellets.Furthermore, INB produces as well rare earth oxides 2 figs., 1 tab.

Global Modeling of Uranium Molecular Species Formation Using Laser-Ablated Plasmas

Science.gov (United States)

Curreli, Davide; Finko, Mikhail; Azer, Magdi; Armstrong, Mike; Crowhurst, Jonathan; Radousky, Harry; Rose, Timothy; Stavrou, Elissaios; Weisz, David; Zaug, Joseph

2016-10-01

Uranium is chemically fractionated from other refractory elements in post-detonation nuclear debris but the mechanism is poorly understood. Fractionation alters the chemistry of the nuclear debris so that it no longer reflects the chemistry of the source weapon. The conditions of a condensing fireball can be simulated by a low-temperature plasma formed by vaporizing a uranium sample via laser heating. We have developed a global plasma kinetic model in order to model the chemical evolution of U/UOx species within an ablated plasma plume. The model allows to track the time evolution of the density and energy of an uranium plasma plume moving through an oxygen atmosphere of given fugacity, as well as other relevant quantities such as average electron and gas temperature. Comparison of model predictions with absorption spectroscopy of uranium-ablated plasmas provide preliminary insights on the key chemical species and evolution pathways involved during the fractionation process. This project was sponsored by the DoD, Defense Threat Reduction Agency, Grant HDTRA1-16-1-0020. This work was performed in part under the auspices of the U.S. DoE by Lawrence Livermore National Laboratory under Contract DE-AC52-07NA27344.

Smoking in uranium enrichment research building in Tokai Research Establishment, Japan Atomic Energy Research Institute

International Nuclear Information System (INIS)

1990-01-01

On the smoking occurred on May 30, 1989 in the uranium enrichment research building, the investigation has been carried out about the presumed cause and the countermeasures for preventing the recurrence, and the following report was presented. In the uranium scrap after the oxidation treatment of vapor-deposited metallic uranium was carried out, a small quantity of unoxidized part having reactivity remained. This unoxidized part existing locally reacts with air in a container, and there is the possibility of generating heat after about one day. In this accident, unoxidized part existed near the wall of a polyethylene vessel, and the oxidation and heat generation reaction advanced. The vessel broke, air supply increased, and heat generation spread. After the temperature reached 300degC, the oxidation of UO 2 to U 3 O 8 took part, thus the polyethylene vessel and others generated smoke. As the countermeasures, for the preservation of uranium scrap, metallic vessels are used, and the atmosphere of inert gas or vacuum is maintained. The uranium scrap containing unoxidized part is rapidly oxidized. The uranium enrichment research building was decontamination. (K.I.)

Uranium sesqui nitride synthesis and its use as catalyst for the thermo decomposition of ammonia

International Nuclear Information System (INIS)

Rocha, Soraya Maria Rizzo da

1996-01-01

The preoccupation to have a secure destination for metallic uranium scraps and wastes and to search new non-nuclear uses for the huge amount of depleted metal uranium accumulated at the nuclear industry encouraged the study of the uranium sesqui nitride synthesis and its use. The use of uranium sesqui nitride as a catalyst for the thermo decomposition of ammonia for the hydrogen production has enormous significance. One of the most important nuclear cycle step is the reduction of the higher uranium oxides for the production of uranium dioxide and its conversion to uranium tetrafluoride. The reduction of the UO 3 and U 3 O 8 oxides is accomplished by the gas-solid reaction with elementary hydrogen. For economical purposes and for the safety concern the nuclear industry prefers to manufacture the hydrogen gas at the local and at the moment of use, exploring the catalytic decomposition of ammonia vapor. Using metallic uranium scraps as the raw material the obtention of its nitride was achieved by the reaction with ammonia. The results of the chemical and physical characterization of the prepared uranium sesqui nitride and its behavior as a catalyst for the cracking of ammonia are commented. A lower ammonia cracking temperature (550 deg C) using the uranium sesqui nitride compared with recommended industrial catalysts iron nitride (650 deg C) and manganese nitride (700 deg C) sounds reliable and economically advantageous. (author)

A new era in U.S. uranium enrichment

International Nuclear Information System (INIS)

Longenecker, J.R.

1984-01-01

Complex market conditions, including lower than anticipated electrical growth rates, creation of a large spot market of enriched uranium, fluctuations in currency exchange rates, and certain political considerations, have created an unstable market for all primary producers, including the United States. In response to these conditions, the Department of Energy made significant changes to the U.S. program including the issuance of the Utility Services contract on January 18, 1984. Other major changes include redirecting research and development efforts on the advanced gas centrifuge and atomic vapor laser isotope separation processes, rescoping of the Gas Centrifuge Enrichment Plant project, and reevaluation of the operational mode of the three gaseous diffusion plants. Taken together, we believe these actions will retain the U.S. position of leadership in uranium enrichment. In summary, we plan to compete--through introduction of the world's most advanced, lowest cost technology and through responsiveness to our customers' needs

Uranium

International Nuclear Information System (INIS)

Hamdoun, N.A.

2007-01-01

The article includes a historical preface about uranium, discovery of portability of sequential fission of uranium, uranium existence, basic raw materials, secondary raw materials, uranium's physical and chemical properties, uranium extraction, nuclear fuel cycle, logistics and estimation of the amount of uranium reserves, producing countries of concentrated uranium oxides and percentage of the world's total production, civilian and military uses of uranium. The use of depleted uranium in the Gulf War, the Balkans and Iraq has caused political and environmental effects which are complex, raising problems and questions about the effects that nuclear compounds left on human health and environment.

Uranium extraction from gold-uranium ores

Energy Technology Data Exchange (ETDEWEB)

Laskorin, B.N.; Golynko, Z.Sh.

1981-01-01

The process of uranium extraction from gold-uranium ores in the South Africa is considered. Flowsheets of reprocessing gold-uranium conglomerates, pile processing and uranium extraction from the ores are presented. Continuous counter flow ion-exchange process of uranium extraction using strong-active or weak-active resins is noted to be the most perspective and economical one. The ion-exchange uranium separation with the succeeding extraction is also the perspective one.

Toxicity evaluation of the effluent of the ammonium diuranate process proceeding from the Uranium Reconversion Cycle (IPEN/CNEN-SP)

International Nuclear Information System (INIS)

Osti, Silvio Cesar de

2001-01-01

This project was developed with the objective to evaluate the acute and chronic toxicity of the ammonium diuranate proceeding from the process used to obtain uranium hexafluoride (UF 6 ), substance which is necessary to produce fuel used by the IEA-R1-IPEN reactor. Five acute toxicity tests were done with Daphnia similis in which concentration values of EC(I)50;48h, between 0,39% and 0,57% of the effluent were determined, and other five with Danio rerio in which concentration values of EC(I)50;48h, between 0,06% and 0,07% of the effluent were determined. Three chronic toxicity tests with Selenastrum capricornutum were done, having found NOEC values for concentrations below 0,12% of the effluents. To determine the ion fluoride toxicity in the Daphnia similis, five acute toxicity tests were done in which values of EC(I)50;48h, between 263.90 mgL -1 and 292.82 mgL -1 were found. The acute toxicity tests done with D. similis demonstrated that the effluent toxicity persisted during its storage period. The acute toxicity test with D.rerio and chronic ones with S. capricornutum using the effluents after the ionic-replace treatment, which objective is to recover uranium for reuse, demonstrated the effluent toxicity persistency. (author)

Field test of short-notice random inspections for inventory-change verification at a low-enriched-uranium fuel-fabrication plant

International Nuclear Information System (INIS)

Fishbone, L.G.; Moussalli, G.; Naegele, G.

1995-01-01

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. Then a statistical inference can be made from verification results for items verified during SNRIs to the entire populations, i.e. the entire strata, even if inspectors were not present when many items were received or produced. A six-month field test of the feasibility of such SNRIs took place at the Westinghouse Electric Corporation Commercial Nuclear Fuel Division during 1993. 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. They arrived unannounced at the plant, in most cases immediately after travel from Canada, where the IAEA maintains a regional office. Items from both strata were verified during the SNRIs by meant of nondestructive assay equipment

The mortality and cancer morbidity experience of workers at the Springfields uranium production facility, 1946-95

International Nuclear Information System (INIS)

McGeoghegan, D.; Binks, K.

2000-01-01

The results presented here are from the follow-up of the cohort of workers ever employed at the Springfields site of British Nuclear Fuels plc (BNFL) between 1946 and 1995. The main activity of the site is uranium fuel fabrication and uranium hexafluoride production. The study cohort consists of 19 454 current and former employees, 13 960 of which were classified as radiation workers, and contains 479 146 person-years of follow-up. The mean follow-up period is 24.6 years. To the end of 1995 there have been 4832 deaths recorded for this cohort, 3476 of which were amongst radiation workers and 1356 were amongst non-radiation workers. The standardised mortality ratios (SMRs) for all causes were 84 and 98 for radiation workers and non-radiation workers respectively. For all cancers the SMRs were 86 and 96 respectively. For cancer morbidity the standardised registration ratios (SRRs) for all cancers were 81 and 81 respectively. Significant associations were noted for both mortality and morbidity due to Hodgkin's disease and cumulative external dose. A strong association was also noted for morbidity, but not mortality, due to non-Hodgkin's lymphoma. These associations, however, are unlikely to be causal. The excess relative risk estimates for cancer other than leukaemia and for leukaemia excluding chronic lymphatic leukaemia are consistent with other occupationally exposed cohorts and estimates from the high-dose studies. (author)

Uranium enrichment by laser: a technology for the future

International Nuclear Information System (INIS)

Cazalet, J.

1999-01-01

The SILVA (Isotopic Separation by Laser on atomic Vapor of uranium) process, developed by CEA and COGEMA, is an innovative system of production of enriched uranium, to be used as the fuel of nuclear reactors. It is a sound research program, calling on advanced technologies that are quickly changing. The goal is to cut drastically the production cost in comparison with the operating cost of the present plants based on gaseous diffusion. its industrialization is forecast for the beginning of next century. The SILVA process consists in putting a vapor of uranium through a beam of photons emitted by finely tuned lasers capable of ionising selectively the isotopes 235. The ionised isotopes are attracted on plates by an electric field, they are condensed and collected on these plates. The very high selectivity of enrichment technologies by laser, which are quite new, pave the way for compact and modular plants, which will consume little energy. Accordingly their production cost will be very low. So a new process could take a significant part of the uranium enrichment market after 2010. Even if the multinational EURODIF gaseous diffusion plant is modern and performing, it will be necessary to strengthen the French industry of uranium enrichment to maintain or improve its competitive position on the world market. This could be achieved by smoothly replacing EURODIF by a high performance laser plant. This is the common goal of CEA and COGEMA: all the efforts are concentrated on SILVA, the qualities of which (high selectivity, separation in one single step) have been demonstrated in the facilities of Saclay and Pierrelatte. 400 researchers and technicians are involved, as well as many industrial firms. The budget is equally by CEA and COGEMA through a cooperation agreement. The program includes: a phase of scientific and technical research, which has been highlighted in 1997-1998 by a demonstration of feasibility of the process; a phase of technological development, with

Method for converting uranium oxides to uranium metal

International Nuclear Information System (INIS)

Duerksen, W.K.

1988-01-01

A method for converting uranium oxide to uranium metal is described comprising the steps of heating uranium oxide in the presence of a reducing agent to a temperature sufficient to reduce the uranium oxide to uranium metal and form a heterogeneous mixture of a uranium metal product and oxide by-products, heating the mixture in a hydrogen atmosphere at a temperature sufficient to convert uranium metal in the mixture to uranium hydride, cooling the resulting uranium hydride-containing mixture to a temperature sufficient to produce a ferromagnetic transition in the uranium hydride, magnetically separating the cooled uranium hydride from the mixture, and thereafter heating the separated uranium hydride in an inert atmosphere to a temperature sufficient to convert the uranium hydride to uranium metal

Simple electrolytic cell for production of elemental fluorine

International Nuclear Information System (INIS)

Dides F, M.; Padilla S, U.

1990-01-01

It was constructed and tested a simple electrolytic cell for the production of elemental fluorine. The fluorine production is essential in the obtainment of uranium hexafluoride, a compound for the nuclear fuel cycle. (A.C.A.S.)

Global Monitoring Of Uranium Hexifloride Cylinders Next Steps In Development Of An Action Plan

International Nuclear Information System (INIS)

Hanks, D.

2010-01-01

Over 40 industrial facilities world-wide use standardized uranium hexafluoride (UF 6 ) cylinders for transport, storage and in-process receiving in support of uranium conversion, enrichment and fuel fabrication processes. UF 6 is processed and stored in the cylinders, with over 50,000 tU of UF 6 transported each year in these International Organization for Standardization (ISO) qualified containers. Although each cylinder is manufactured to an ISO standard that calls for a nameplate with the manufacturer's identification number (ID) and the owner's serial number engraved on it, these can be quite small and difficult to read. Recognizing that each facility seems to use a different ID, a cylinder can have several different numbers recorded on it by means of metal plates, sticky labels, paint or even marker pen as it travels among facilities around the world. The idea of monitoring movements of UF 6 cylinders throughout the global uranium fuel cycle has become a significant issue among industrial and safeguarding stakeholders. Global monitoring would provide the locations, movements, and uses of cylinders in commercial nuclear transport around the world, improving the efficiency of industrial operations while increasing the assurance that growing nuclear commerce does not result in the loss or misuse of cylinders. It should be noted that a unique ID (UID) attached to a cylinder in a verifiable manner is necessary for safeguarding needs and ensuring positive ID, but not sufficient for an effective global monitoring system. Modern technologies for tracking and inventory control can pair the UID with sensors and secure data storage for content information and complete continuity of knowledge over the cylinder. This paper will describe how the next steps in development of an action plan for employing a global UF 6 cylinder monitoring network could be cultivated using four primary UID functions - identification, tracking, controlling, and accounting.

DUF6 Materials Use Roadmap

International Nuclear Information System (INIS)

Haire, M.J.

2002-01-01

The U.S. government has ∼500,000 metric tons (MT) of surplus depleted uranium (DU) in various chemical forms stored at U.S. Department of Energy (DOE) sites across the United States. This DU, most of which is DU hexafluoride (DUF 6 ) resulting from uranium enrichment operations, is the largest amount of nuclear material in DOE's inventory. On July 6, 1999, DOE issued the ''Final Plan for the Conversion of Depleted Uranium Hexafluoride as required by Public Law 105-204'', in which DOE committed to develop a ''Depleted Uranium Hexafluoride Materials Use Roadmap'' in order to establish a strategy for the products resulting from conversion of DUF 6 to a stable form. This report meets the commitment in the Final Plan by providing a comprehensive roadmap that DOE will use to guide any future research and development activities for the materials associated with its DUF 6 inventory. The Roadmap supports the decision presented in the ''Record of Decision for Long-Term Management and Use of Depleted Uranium Hexafluoride'', namely to begin conversion of the DUF 6 inventory as soon as possible, either to uranium oxide, uranium metal, or a combination of both, while allowing for future uses of as much of this inventory as possible. In particular, the Roadmap is intended to explore potential uses for the DUF 6 conversion products and to identify areas where further development work is needed. It focuses on potential governmental uses of DUF 6 conversion products but also incorporates limited analysis of using the products in the private sector. The Roadmap builds on the analyses summarized in the recent ''Programmatic Environmental Impact Statement for Alternative Strategies for the Long-Term Management and Use of Depleted Uranium Hexafluoride''. It also addresses other surplus DU, primarily in the form of DU trioxide and DU tetrafluoride. The DU-related inventory considered here includes the following: (1) Components directly associated with the DUF 6 presently being stored

NRC licensing of uranium enrichment plants

International Nuclear Information System (INIS)

Moran, B.W.

1991-01-01

The US Nuclear Regulatory Commission (NRC) is preparing a rule making that establishes the licensing requirements for low-enriched uranium enrichment plants. Although implementation of this rule making is timed to correspond with receipt of a license application for the Louisiana Energy Services centrifuge enrichment plant, the rule making is applicable to all uranium enrichment technologies. If ownership of the US gaseous diffusion plants and/or atomic vapor laser isotope separation is transferred to a private or government corporation, these plants also would be licensable under the new rule making. The Safeguards Studies Department was tasked by the NRC to provide technical assistance in support of the rule making and guidance preparation process. The initial and primary effort of this task involved the characterization of the potential safeguards concerns associated with a commercial enrichment plant, and the licensing issues associated with these concerns. The primary safeguards considerations were identified as detection of the loss of special nuclear material, detection of unauthorized production of material of low strategic significance, and detection of production of uranium enriched to >10% 235 U. The primary safeguards concerns identified were (1) large absolute limit of error associated with the material balance closing, (2) the inability to shutdown some technologies to perform a cleanout inventory of the process system, and (3) the flexibility of some technologies to produce higher enrichments. Unauthorized production scenarios were identified for some technologies that could prevent conventional material control and accounting programs from detecting the production and removal of 5 kg 235 U as highly enriched uranium. Safeguards techniques were identified to mitigate these concerns

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.

75 FR 67086 - Proposed Subsequent Arrangement

Science.gov (United States)

2010-11-01

... concerns the retransfer of 1,470,588.2 kg of U.S.-origin natural uranium hexafluoride (68.00% U), 1,000,000... Areva Resources, will be transferred to Eurodif Production for enrichment and use as fuel in civilian...

75 FR 67087 - Proposed Subsequent Arrangement

Science.gov (United States)

2010-11-01

... concerns the retransfer of 514,705.9 kg of U.S.-origin natural uranium hexafluoride (68.00% U), 350,000 kg... be transferred to URENCO-Gronau for enrichment and use as fuel in civilian nuclear power programs in...

Development of Liquid-Vapor Core Reactors with MHD Generator for Space Power and Propulsion Applications

International Nuclear Information System (INIS)

Samim Anghaie

2002-01-01

Any reactor that utilizes fuel consisting of a fissile material in a gaseous state may be referred to as a gaseous core reactor (GCR). Studies on GCRs have primarily been limited to the conceptual phase, mostly due to budget cuts and program cancellations in the early 1970's. A few scientific experiments have been conducted on candidate concepts, primarily of static pressure fissile gas filling a cylindrical or spherical cavity surrounded by a moderating shell, such as beryllium, heavy water, or graphite. The main interest in this area of nuclear power generation is for space applications. The interest in space applications has developed due to the promise of significant enhancement in fuel utilization, safety, plant efficiency, special high-performance features, load-following capabilities, power conversion optimization, and other key aspects of nuclear power generation. The design of a successful GCR adapted for use in space is complicated. The fissile material studied in the pa st has been in a fluorine compound, either a tetrafluoride or a hexafluoride. Both of these molecules have an impact on the structural material used in the making of a GCR. Uranium hexafluoride as a fuel allows for a lower operating temperature, but at temperatures greater than 900K becomes essentially impossible to contain. This difficulty with the use of UF6 has caused engineers and scientists to use uranium tetrafluoride, which is a more stable molecule but has the disadvantage of requiring significantly higher operating temperatures. Gas core reactors have traditionally been studied in a steady state configuration. In this manner a fissile gas and working fluid are introduced into the core, called a cavity, that is surrounded by a reflector constructed of materials such as Be or BeO. These reactors have often been described as cavity reactors because the density of the fissile gas is low and criticality is achieved only by means of the reflector to reduce neutron leakage from the core

Uranium

International Nuclear Information System (INIS)

Cuney, M.; Pagel, M.; Leroy, J.

1992-01-01

First, this book presents the physico-chemical properties of Uranium and the consequences which can be deduced from the study of numerous geological process. The authors describe natural distribution of Uranium at different scales and on different supports, and main Uranium minerals. A great place in the book is assigned to description and classification of uranium deposits. The book gives also notions on prospection and exploitation of uranium deposits. Historical aspects of Uranium economical development (Uranium resources, production, supply and demand, operating costs) are given in the last chapter. 7 refs., 17 figs

Metal-free reduction of the greenhouse gas sulfur hexafluoride, formation of SF5 containing ion pairs and the application in fluorinations

KAUST Repository

Rueping, Magnus

2017-05-04

A protocol for the fast and selective two-electron reduction of the potent greenhouse gas sulfur hexafluoride (SF6) by organic electron donors at ambient temperature has been developed. The reaction yields solid ion pairs consisting of donor dications and SF5-anions which can be effectively used in fluorination reactions.

Uranium