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1

Preparation of uranium compounds  

DOE Patents [OSTI]

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

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

2013-02-19T23:59:59.000Z

2

Conversion of depleted uranium hexafluoride to a solid uranium compound  

DOE Patents [OSTI]

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

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

2001-01-01T23:59:59.000Z

3

Uranium Compounds and Other Natural Radioactivities  

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

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

4

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

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

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

5

Dissolution rates of uranium compounds in simulated lung fluid  

SciTech Connect (OSTI)

Maximum dissolution rates of uranium into simulated lung fluid from a variety of materials were measured at 37/sup 0/in the where f/sub i/ is in order to estimate clearance rates from the deep lung. A batch procedure was utilized in which samples containing as little as 10 ..mu..g of natural uranium could be tested. The materials included: products of uranium mining, milling and refining operations, coal fly ash, an environmental sample from a site exposed to multiple uranium sources, and purified samples of (NH/sub 4/)/sub 2/U/sub 2/O/sub 7/ U/sub 3/O/sub 8/, UO/sub 2/, and UF/sub 4/. Dissolution of uranium from several materials indicated the presence of more than one type of uranium compound; but in all cases, the fraction F of uranium remaining undissolved at any time t could be represented by the sum of up to three terms in the series: F = ..sigma../sub i/f/sub i/ exp (-0.693t/UPSILON/sub i/), where f/sub i/ is the initial fraction of component i with dissolution half-time epsilon/sub i/. Values of epsilon/sub i/ varied from 0.01 day to several thousand days depending on the physical and chemical form of the uranium. Dissolution occurred predominantly by formation of the (UO/sub 2/(CO/sub 3/)/sub 3/)/sup 4 -/ ion; and as a result, tetravalent uranium compounds dissolved slowly. Dissolution rates of size-separated yellow-cake aerosols were found to be more closely correlated with specific surface area than with aerodynamic diameter.

Kalkwarf, D.R.

1981-01-01T23:59:59.000Z

6

Derivation of uranium residual radioactive material guidelines for the Shpack site  

SciTech Connect (OSTI)

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

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

1991-08-01T23:59:59.000Z

7

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

E-Print Network [OSTI]

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

Svane, Axel Torstein

8

Containment of uranium in the proposed Egyptian geologic repository for radioactive waste using hydroxyapatite.  

SciTech Connect (OSTI)

Currently, the Egyptian Atomic Energy Authority is designing a shallow-land disposal facility for low-level radioactive waste. To insure containment and prevent migration of radionuclides from the site, the use of a reactive backfill material is being considered. One material under consideration is hydroxyapatite, Ca{sub 10}(PO{sub 4}){sub 6}(OH){sub 2}, which has a high affinity for the sorption of many radionuclides. Hydroxyapatite has many properties that make it an ideal material for use as a backfill including low water solubility (K{sub sp}>10{sup -40}), high stability under reducing and oxidizing conditions over a wide temperature range, availability, and low cost. However, there is often considerable variation in the properties of apatites depending on source and method of preparation. In this work, we characterized and compared a synthetic hydroxyapatite with hydroxyapatites prepared from cattle bone calcined at 500 C, 700 C, 900 C and 1100 C. The analysis indicated the synthetic hydroxyapatite was similar in morphology to 500 C prepared cattle hydroxyapatite. With increasing calcination temperature the crystallinity and crystal size of the hydroxyapatites increased and the BET surface area and carbonate concentration decreased. Batch sorption experiments were performed to determine the effectiveness of each material to sorb uranium. Sorption of U was strong regardless of apatite type indicating all apatite materials evaluated. Sixty day desorption experiments indicated desorption of uranium for each hydroxyapatite was negligible.

Moore, Robert Charles; Hasan, Ahmed Ali Mohamed; Headley, Thomas Jeffrey; Sanchez, Charles Anthony (University of Arizona, Yuma, AZ); Zhao, Hongting; Salas, Fred Manuel; Hasan, Mahmoud A. (Egyptian Atomic Energy Authority, Cairo, Egypt); Holt, Kathleen Caroline

2004-04-01T23:59:59.000Z

9

Reaction of Tris(cyclopentadienyl)uranium compounds with amines, azides, and related ligands  

SciTech Connect (OSTI)

The trivalent uranium compound, (MeC{sub 5}H{sub 4}){sub 3}U(thf), serves as a one- or two-electron reducing agent towards azides, RN{sub 3}. These reactions produce either the uranium(IV) azide, (MeC{sub 5}H{sub 4}){sub 3}UN{sub 3}, or uranium(V) imides, (MeC{sub 5}H{sub 4}){sub 3}UNR. The role of steric and electronic effects upon this reaction has been investigated using several series of azides. For Me{sub 3}XN{sub 3}, the imides are produced when X = C or Si, both products are formed when X = Ge, and the azide is produced when X = Sn. For Ph{sub 3}XN{sub 3}, the azide is produced when X = C or Sn. For Ph{sub 3-x}CH{sub 3}N{sub 3}, the imide is produced when x = 2 and both compounds are produced when x = 1. For substituted phenylazides, RC{sub 6}H{sub 4}N{sub 3}, only the imides are produced. The magnetic properties of uranium diimides, ((MeC{sub 5}H{sub 4}){sub 3}U){sub 2}({mu}-NRN), were investigated. Several uranium(III) amines, (MeC{sub 5}H{sub 4}){sub 3}U(NH{sub 2}R), were produced from (MeC{sub 5}H{sub 4}){sub 3}U(thf) and RNH{sub 2}, and NH{sub 3} was found to be a better ligand towards (MeC{sub 5}H{sub 4}){sub 3}U than is PMe{sub 3}.

Rosen, R.K.

1989-12-01T23:59:59.000Z

10

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

E-Print Network [OSTI]

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

Lawrence, Jon

11

Uranium Ore Uranium is extracted  

E-Print Network [OSTI]

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

12

Derivation of residual radioactive material guidelines for uranium in soil at the Middlesex Sampling Plant Site, Middlesex, New Jersey  

SciTech Connect (OSTI)

Residual radioactive material guidelines for uranium in soil were derived for the Middlesex Sampling Plant (MSP) site in Middlesex, New Jersey. This site has been designated for remedial action under the Formerly Utilized Sites Remedial Action Program (FUSRAP) of the US Department of Energy. The site became contaminated from operations conducted in support of the Manhattan Engineer District (MED) and the Atomic Energy Commission (AEC) between 1943 and 1967. Activities conducted at the site included sampling, storage, and shipment of uranium, thorium, and beryllium ores and residues. Uranium guidelines for single radioisotopes and total uranium were derived on the basis of the requirement that the 50-year committed effective dose equivalent to a hypothetical individual living or working in the immediate vicinity of the MSP site should not exceed a dose of 30 mrem/yr following remedial action for the current-use and likely future-use scenarios or a dose of 100 mrem/yr for less likely future-use scenarios. The RESRAD computer code, which implements the methodology described in the DOE manual for establishing residual radioactive material guidelines, was used in this evaluation. Four scenarios were considered for the site. These scenarios vary regarding future land use at the site, sources of water used, and sources of food consumed.

Dunning, D.E. [Argonne National Lab., IL (United States). Environmental Assessment Div.

1995-02-01T23:59:59.000Z

13

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

E-Print Network [OSTI]

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

Hwang, Chiachi

2009-01-01T23:59:59.000Z

14

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

E-Print Network [OSTI]

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 ...

American Society for Testing and Materials. Philadelphia

2010-01-01T23:59:59.000Z

15

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

SciTech Connect (OSTI)

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

Forsberg, C.W.

1997-02-19T23:59:59.000Z

16

Acute and chronic toxicity of uranium compounds to Ceriodaphnia-Daphnia dubia  

SciTech Connect (OSTI)

A study to determine the acute and chronic toxicity of uranyl nitrate, hydrogen uranyl phosphate, and uranium dioxide to the organism Ceriodaphnia dubia was conducted. The toxicity tests were conducted by two independent environmental consulting laboratories. Part of the emphasis for this determination was based on concerns expressed by SCDHEC, which was concerned that a safety factor of 100 must be applied to the previous 1986 acute toxicity result of 0.22 mg/L for Daphnia pulex, This would have resulted in the LETF release limits being based on an instream concentration of 0.0022 mg/L uranium. The NPDES Permit renewal application to SCDHEC utilized the results of this study and recommended that the LETF release limit for uranium be based an instream concentration of 0.004 mg/L uranium. This is based on the fact that the uranium releases from the M-Area LETF will be in the hydrogen uranyl phosphate form, or a uranyl phosphate complex at the pH (6--10) of the Liquid Effluent Treatment Facility effluent stream, and at the pH of the receiving stream (5.5 to 7.0). Based on the chronic toxicity of hydrogen uranyl phosphate, a lower uranium concentration limit for the Liquid Effluent Treatment Facility outfall vs. the existing NPDES permit was recommended: The current NPDES permit ``Guideline`` for uranium at outfall M-004 is 0.500 mg/L average and 1.0 mg/L maximum, at a design flowrate of 60 gpm. It was recommended that the uranium concentration at the M-004 outfall be reduced to 0.28 mg/L average, and 0.56 mg/L, maximum, and to reduce the design flowrate to 30 gpm. The 0.28 mg/L concentration will provide an instream concentration of 0.004 mg/L uranium. The 0.28 mg/L concentration at M-004 is based on the combined flows from A-014, A-015, and A-011 outfalls (since 1985) of 1840 gpm (2.65 MGD) and was the flow rate which was utilized in the 1988 NPDES permit renewal application.

Pickett, J.B.; Specht, W.L.; Keyes, J.L.

1993-03-31T23:59:59.000Z

17

JOURNAL DE PHYSIQUE Colloque C4, supplment au n" 4, Tome 40, avril 1979, page C4-142 Magnetic neutron scattering on intermetallic uranium compounds (*)  

E-Print Network [OSTI]

neutron scattering on intermetallic uranium compounds (*) M. Loewenhaupt (f ), S. Horn (**), F. Steglich.- Abstract. -- We report on inelastic neutron scattering experiments performed in the temperature range 5 K quasielastic line. Using thermal neutrons, no inelastic contributions to the magnetic scattering could

Paris-Sud XI, Université de

18

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

E-Print Network [OSTI]

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

Minarik, William

19

Lead, Uranium, and Nickel Compound Data from the XAFS Library at the Stanford Synchrotron Radiation Laboratory (SSRL)  

DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

The x-ray absorption fine structure spectroscopy (XAFS) library at the Stanford Synchrotron Radiation Laboratory is intended to be a reference library of XAFS spectra for various lead, uranium, and nickel compounds. Compounds are organized by central atom and all spectra are transmission data. Molecular Environmental Science (MES) research at SSRL focuses on the fundamental interfacial, molecular- and nano-scale processes that control contaminant and nutrient cycling in the biosphere with the goal of elucidating global elemental cycles and anthropogenic influences on the environment. Key areas of investigation include the: (a) Structural chemistry of water and dissolved solutes, (b) Structural chemistry and reactivity of complex natural environmental materials with respect to heavy metals and metalloids (biominerals, Fe- and Mn-oxides, biofilms, and organic materials), (c) Reactions at environmental interfaces, including sorption, precipitation and dissolution processes that affect the bioavailability of heavy metals and other contaminants, and (d) Microbial transformations of metals and anions. SSRL-based MES research utilizes synchrotron-based x-ray absorption spectroscopy (XAS), x-ray diffraction (XRD), small-angle x-ray scattering (SAXS), x-ray standing wave (XSW) spectroscopy, and photoemission spectroscopy (PES) because of their unique capabilities to probe structure/composition relationships in complex, non-crystalline, and dilute materials. [copied from http://www-ssrl.slac.stanford.edu/mes/index.html

20

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

E-Print Network [OSTI]

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

Hwang, Chiachi

2009-01-01T23:59:59.000Z

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


21

Microcalorimetric measurement of reaction enthalpies in solutions of uranium and neptunium compounds  

SciTech Connect (OSTI)

The formation of complexes of uranyl and neptunyl(VI) ions with carbonate and hydrogen carbonate has been studied by titration microcalorimetry. The measurements were carried out with a computer-controlled microcalorimeter which is described in detail. Sample volumes are typically in the range of 1.5 to 2.5 ccm, containing about 0.05 millimole of the ionic species to be studied. The small volume renders the calorimeter useful for the measurement of uncommon and strongly radioactive substances. Enthalpies of reaction were obtained for the formation of the dicarbonato and the tricarbonato uranyl ions in a sulfate medium of ionic strength 1.6. The enthalpies are ..delta..H/sub 2/ = -39.6 +- 1 kJ/mol and -57.5 +- 1.5 kJ/mol, respectively. The titration data for the neptunyl(VI) - carbonate system yield a value of -50 +- 2 kJ/mol for the tricarbonato-neptunyl ion when interpreted in analogy to the uranyl system.

Schreiner, F.; Friedman, A.M.; Richards, R.R.; Sullivan, J.C.

1984-01-01T23:59:59.000Z

22

Technology for Treatment of Liquid Radioactive Waste Generated during Uranium and Plutonium Chemical and Metallurgical Manufacturing in FSUE PO Mayak - 13616  

SciTech Connect (OSTI)

Created technological scheme for treatment of liquid radioactive waste generated while uranium and plutonium chemical and metallurgical manufacturing consists of: - Liquid radioactive waste (LRW) purification from radionuclides and its transfer into category of manufacturing waste; - Concentration of suspensions containing alpha-nuclides and their further conversion to safe dry state (calcinate) and moving to long controlled storage. The following technologies are implemented in LRW treatment complex: - Settling and filtering technology for treatment of liquid intermediate-level waste (ILW) with volume about 1500m{sup 3}/year and alpha-activity from 10{sup 6} to 10{sup 8} Bq/dm{sup 3} - Membrane and sorption technology for processing of low-level waste (LLW) of radioactive drain waters with volume about 150 000 m{sup 3}/year and alpha-activity from 10{sup 3} to 10{sup 4} Bq/dm{sup 3}. Settling and filtering technology includes two stages of ILW immobilization accompanied with primary settling of radionuclides on transition metal hydroxides with the following flushing and drying of the pulp generated; secondary deep after settling of radionuclides on transition metal hydroxides with the following solid phase concentration by the method of tangential flow ultrafiltration. Besides, the installation capacity on permeate is not less than 3 m{sup 3}/h. Concentrates generated are sent to calcination on microwave drying (MW drying) unit. Membrane and sorption technology includes processing of averaged sewage flux by the method of tangential flow ultrafiltration with total capacity of installations on permeate not less than 18 m{sup 3}/h and sorption extraction of uranium from permeate on anionite. According to radionuclide contamination level purified solution refers to general industrial waste. Concentrates generated during suspension filtering are evaporated in rotary film evaporator (RFE) in order to remove excess water, thereafter they are dried on infrared heating facility. Solid concentrate produced is sent for long controlled storage. Complex of the procedures carried out makes it possible to solve problems on treatment of LRW generated while uranium and plutonium chemical and metallurgical manufacturing in Federal State Unitary Enterprise (FSUE) Mayak and cease its discharge into open water reservoirs. (authors)

Adamovich, D. [SUE MosSIA Radon, 2/14 7th Rostovsky lane, Moscow, 119121 (Russian Federation)] [SUE MosSIA Radon, 2/14 7th Rostovsky lane, Moscow, 119121 (Russian Federation); Batorshin, G.; Logunov, M.; Musalnikov, A. [FSUE 'PO Mayak', 31 av. Lenin, Ozyorsk, Chelyabinsk region, 456780 (Russian Federation)] [FSUE 'PO Mayak', 31 av. Lenin, Ozyorsk, Chelyabinsk region, 456780 (Russian Federation)

2013-07-01T23:59:59.000Z

23

High loading uranium fuel plate  

DOE Patents [OSTI]

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

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

1990-01-01T23:59:59.000Z

24

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  

SciTech Connect (OSTI)

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.

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

1983-03-01T23:59:59.000Z

25

4.0 RISK FROM URANIUM MINING WASTE IN BUILDING In general, building materials contain low levels of radioactivity. For example, the range of  

E-Print Network [OSTI]

4.0 RISK FROM URANIUM MINING WASTE IN BUILDING MATERIALS In general, building materials contain low, especially in buildings constructed with materials containing uranium TENORM mine wastes. In the Grand the wastes from uranium mines have been removed from mining sites and used in local and nearby communities

26

Uranium Mill Tailings Management  

SciTech Connect (OSTI)

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

Nelson, J.D.

1982-01-01T23:59:59.000Z

27

E-Print Network 3.0 - alkaline radioactive liquid Sample Search...  

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

with Conventional Uranium Milling Introduction Summary: Radioactive Materials from Uranium Mining. Volume 1: Mining and Reclamation Background" by U.S. EPA (2006... as an...

28

Raman Investigation of The Uranium Compounds U3O8, UF4, UH3 and UO3 under Pressure at Room Temperature  

SciTech Connect (OSTI)

Our current state-of-the-art X-ray diffraction experiments are primarily sensitive to the position of the uranium atom. While the uranium - low-Z element bond (such as U-H or U-F) changes under pressure and temperature the X-ray diffraction investigations do not reveal information about the bonding or the stoichiometry. Questions that can be answered by Raman spectroscopy are (i) whether the bonding strength changes under pressure, as observed by either blue- or red-shifted peaks of the Raman active bands in the spectrum and (ii) whether the low-Z element will eventually be liberated and leave the host lattice, i.e. do the fluorine, oxygen, or hydrogen atoms form dimers after breaking the bond to the uranium atom. Therefore Raman spectra were also collected in the range where those decomposition products would appear. Raman is particularly well suited to these types of investigations due to its sensitivity to trace amounts of materials. One challenge for Raman investigations of the uranium compounds is that they are opaque to visible light. They absorb the incoming radiation and quickly heat up to the point of decomposition. This has been dealt with in the past by keeping the incoming laser power to very low levels on the tens of milliWatt range consequently affecting signal to noise. Recent modern investigations also used very small laser spot sizes (micrometer range) but ran again into the problem of heating and chemical sensitivity to the environment. In the studies presented here (in contrast to all other studies that were performed at ambient conditions only) we employ micro-Raman spectroscopy of samples situated in a diamond anvil cell. This increases the trustworthiness of the obtained data in several key-aspects: (a) We surrounded the samples in the DAC with neon as a pressure transmitting medium, a noble gas that is absolutely chemically inert. (b) Through the medium the sample is thermally heat sunk to the diamond anvils, diamond of course possessing the very best heat conductivity of any material. Therefore local heating and decomposition are avoided, a big challenge with other approaches casting doubts on their results. (c) This in turn benefits the signal/noise ratio tremendously since the Raman features of uranium-compounds are very small. The placement of the samples in DACs allows for higher laser powers to impinge on the sample spot while keeping the spot-size larger than in previous studies and keep the samples from heating up. Raman spectroscopy is a very sensitive non-invasive technique and we will show that it is even possible to distinguish the materials by their origin / manufacturer as we have studied samples from Cameco (Canada) and IBI-Labs (US-Florida) and can compare with ambient literature data for samples from Strem (US-MA) and Areva (Pierrelatte, France).

Lipp, M J; Jenei, Z; Park-Klepeis, J; Evans, W J

2011-12-15T23:59:59.000Z

29

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

SciTech Connect (OSTI)

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

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

2011-01-01T23:59:59.000Z

30

Magnetic Exchange Coupling and Single-Molecule Magnetism in Uranium Complexes  

E-Print Network [OSTI]

greater than 99% U-238 (depleted uranium), which has no neturanium, since this actinide element offers minimal radioactivity (in depleted

Rinehart, Jeffrey Dennis

2010-01-01T23:59:59.000Z

31

Radioactive Waste Radioactive Waste  

E-Print Network [OSTI]

#12;Radioactive Waste at UF Bldg 831 392-8400 #12;Radioactive Waste · Program is designed to;Radioactive Waste · Program requires · Generator support · Proper segregation · Packaging · labeling #12;Radioactive Waste · What is radioactive waste? · Anything that · Contains · or is contaminated

Slatton, Clint

32

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  

E-Print Network [OSTI]

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...

American Society for Testing and Materials. Philadelphia

2004-01-01T23:59:59.000Z

33

activity radioactive waste: Topics by E-print Network  

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

is: not high-level radioactive waste or irradiated nuclear fuel not uranium, thorium or other ore tailings or waste from extraction and concentration for source material...

34

aqueous radioactive waste: Topics by E-print Network  

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

is: not high-level radioactive waste or irradiated nuclear fuel not uranium, thorium or other ore tailings or waste from extraction and concentration for source material...

35

acidic radioactive waste: Topics by E-print Network  

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

is: not high-level radioactive waste or irradiated nuclear fuel not uranium, thorium or other ore tailings or waste from extraction and concentration for source material...

36

activities radioactive waste: Topics by E-print Network  

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

is: not high-level radioactive waste or irradiated nuclear fuel not uranium, thorium or other ore tailings or waste from extraction and concentration for source material...

37

activity radioactive wastes: Topics by E-print Network  

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

is: not high-level radioactive waste or irradiated nuclear fuel not uranium, thorium or other ore tailings or waste from extraction and concentration for source material...

38

Magnetic Exchange Coupling and Single-Molecule Magnetism in Uranium Complexes  

E-Print Network [OSTI]

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

Rinehart, Jeffrey Dennis

2010-01-01T23:59:59.000Z

39

Uranium Mill Tailings Remedial Action Project surface project management plan  

SciTech Connect (OSTI)

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

Not Available

1994-09-01T23:59:59.000Z

40

EPA Uranium Program Update Loren W. Setlow and  

E-Print Network [OSTI]

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

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


41

Soil to plant transfer of 238 Th on a uranium  

E-Print Network [OSTI]

Soil to plant transfer of 238 U, 226 Ra and 232 Th on a uranium mining-impacted soil from species grown in soils from southeastern China contaminated with uranium mine tailings were analyzed The radioactive waste (e.g. tailings) produced by uranium mining activities contains a series of long

Hu, Qinhong "Max"

42

Modeling Uranium-Proton Ion Exchange in Biosorption  

E-Print Network [OSTI]

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

Volesky, Bohumil

43

Understanding radioactive waste  

SciTech Connect (OSTI)

This document contains information on all aspects of radioactive wastes. Facts are presented about radioactive wastes simply, clearly and in an unbiased manner which makes the information readily accessible to the interested public. The contents are as follows: questions and concerns about wastes; atoms and chemistry; radioactivity; kinds of radiation; biological effects of radiation; radiation standards and protection; fission and fission products; the Manhattan Project; defense and development; uses of isotopes and radiation; classification of wastes; spent fuels from nuclear reactors; storage of spent fuel; reprocessing, recycling, and resources; uranium mill tailings; low-level wastes; transportation; methods of handling high-level nuclear wastes; project salt vault; multiple barrier approach; research on waste isolation; legal requiremnts; the national waste management program; societal aspects of radioactive wastes; perspectives; glossary; appendix A (scientific American articles); appendix B (reference material on wastes). (ATT)

Murray, R.L.

1981-12-01T23:59:59.000Z

44

Short Communication Bioreduction and precipitation of uranium in ionic liquid aqueous  

E-Print Network [OSTI]

with uranium from mining and milling operations, radioactive wastes, and from nuclear accidents is a majorShort Communication Bioreduction and precipitation of uranium in ionic liquid aqueous solution t s Uranium forms various complexes with ionic liquids. Uranium bioreduction was affected by the type

Ohta, Shigemi

45

Review The Toxicity of Depleted Uranium  

E-Print Network [OSTI]

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

Wayne Briner

46

An Assessment of the Stability and the Potential for In-Situ Synthesis of Regulated Organic Compounds in High Level Radioactive Waste Stored at Hanford, Richland, Washington  

SciTech Connect (OSTI)

The stability assessment examined 269 non-detected regulated compounds, first seeking literature references of the stability of the compounds, then evaluating each compound based upon the presence of functional groups using professional judgment. Compounds that could potentially survive for significant periods in the tanks (>1 year) were designated as stable. Most of the functional groups associated with the regulated organic compounds were considered unstable under tank waste conditions. The general exceptions with respect to functional group stability are some simple substituted aromatic and polycyclic aromatic compounds that resist oxidation and the multiple substituted aliphatic and aromatic halides that hydrolyze or dehydrohalogenate slowly under tank waste conditions. One-hundred and eighty-one (181) regulated, organic compounds were determined as likely unstable in the tank waste environment.

Wiemers, K.D.; Babad, H.; Hallen, R.T.; Jackson, L.P.; Lerchen, M.E.

1999-01-04T23:59:59.000Z

47

E-Print Network 3.0 - atmospheric radioactivity madrid Sample...  

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

elements "decay." Decay occurs as an element changes to another element, e... .g. uranium to lead. The parent element is radioactive, the daughter element is ... Source:...

48

Uranium from seawater  

SciTech Connect (OSTI)

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

Gregg, D.; Folkendt, M.

1982-09-21T23:59:59.000Z

49

Uranium industry annual 1997  

SciTech Connect (OSTI)

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

NONE

1998-04-01T23:59:59.000Z

50

URANIUM IN ALKALINE ROCKS  

E-Print Network [OSTI]

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

Murphy, M.

2011-01-01T23:59:59.000Z

51

Radioactivity in food crops  

SciTech Connect (OSTI)

Published levels of radioactivity in food crops from 21 countries and 4 island chains of Oceania are listed. The tabulation includes more than 3000 examples of 100 different crops. Data are arranged alphabetically by food crop and geographical origin. The sampling date, nuclide measured, mean radioactivity, range of radioactivities, sample basis, number of samples analyzed, and bibliographic citation are given for each entry, when available. Analyses were reported most frequently for /sup 137/Cs, /sup 40/K, /sup 90/Sr, /sup 226/Ra, /sup 228/Ra, plutonium, uranium, total alpha, and total beta, but a few authors also reported data for /sup 241/Am, /sup 7/Be, /sup 60/Co, /sup 55/Fe, /sup 3/H, /sup 131/I, /sup 54/Mn, /sup 95/Nb, /sup 210/Pb, /sup 210/Po, /sup 106/Ru, /sup 125/Sb, /sup 228/Th, /sup 232/Th, and /sup 95/Zr. Based on the reported data it appears that radioactivity from alpha emitters in food crops is usually low, on the order of 0.1 Bq.g/sup -1/ (wet weight) or less. Reported values of beta radiation in a given crop generally appear to be several orders of magnitude greater than those of alpha emitters. The most striking aspect of the data is the great range of radioactivity reported for a given nuclide in similar food crops with different geographical origins.

Drury, J.S.; Baldauf, M.F.; Daniel, E.W.; Fore, C.S.; Uziel, M.S.

1983-05-01T23:59:59.000Z

52

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

Broader source: Energy.gov [DOE]

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

53

Scrap uranium recycling via electron beam melting  

SciTech Connect (OSTI)

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

McKoon, R.

1993-11-01T23:59:59.000Z

54

Uranium in granites from the southwestern United States: actinide parent-daughter systems, sites and mobilization. Second year report. National Uranium Resource Evaluation  

SciTech Connect (OSTI)

Results of detailed field and laboratory studies are reported on the primary distribution of uranium (and thorium and lead) in the radioactive minerals of five radioactive granite bodies in Arizona and California. This distribution was examined in a granite pluton. Granites with uranium concentrations ranging from 4 to 47 ppM, thorium concentrations from 11 to 181 ppM, and Th/U ratios of 0.6 to 16.0 were compared. Evidence for secondary mobilization, migration, fixation and/or loss of uranium, thorium and radiogenic leads was explored. Uranium distribution in radioactive granites is hosted in a far greater diversity of sites than has previously been known. Uranium and thorium distribution in primary minerals of granites is almost entirely a disequilibrium product involving local fractionation processes during magmatic crystallization. Every radioactive granite studied contains minerals that contain uranium and/or thorium as major stoichiometric components. When the granites are subject to secondary geochemical events and processes, the behavior of uranium is determined by the stability fields of the different radioactive minerals in the rocks. The two most powerful tools for evaluating uranium migration in a granite are (a) isotope dilution mass spectrometry and (b) the electron microprobe. Uranium mobilization and loss is a common feature in radioactive granites of the southwestern United States. A model for the evaluation of uranium loss from granites has been developed. The mineral zircon can be used as an independent indicator of uranium and thorium endowment. The weathering products show surprising differences in the response of different granites in arid region settings. Significant losses of primary uranium (up to 70%) has been a common occurrence. Uranium, thorium and radiogenic lead exist in labile (movable) form on surfaces of cleavages, fractures and grain boundaries in granites.

Silver, L.T.; Woodhead, J.A.; Williams, I.S.; Chappell, B.W.

1984-09-01T23:59:59.000Z

55

Special Analysis for the Disposal of the Consolidated Edison Uranium Solidification Project Waste Stream at the Area 5 Radioactive Waste Management Site, Nevada National Security Site, Nye County, Nevada  

SciTech Connect (OSTI)

The purpose of this Special Analysis (SA) is to determine if the Oak Ridge (OR) Consolidated Edison Uranium Solidification Project (CEUSP) uranium-233 (233U) waste stream (DRTK000000050, Revision 0) is acceptable for shallow land burial (SLB) at the Area 5 Radioactive Waste Management Site (RWMS) on the Nevada National Security Site (NNSS). The CEUSP 233U waste stream requires a special analysis because the concentrations of thorium-229 (229Th), 230Th, 232U, 233U, and 234U exceeded their NNSS Waste Acceptance Criteria action levels. The acceptability of the waste stream is evaluated by determining if performance assessment (PA) modeling provides a reasonable expectation that SLB disposal is protective of human health and the environment. The CEUSP 233U waste stream is a long-lived waste with unique radiological hazards. The SA evaluates the long-term acceptability of the CEUSP 233U waste stream for near-surface disposal as a two tier process. The first tier, which is the usual SA process, uses the approved probabilistic PA model to determine if there is a reasonable expectation that disposal of the CEUSP 233U waste stream can meet the performance objectives of U.S. Department of Energy Manual DOE M 435.1-1, Radioactive Waste Management, for a period of 1,000 years (y) after closure. The second tier addresses the acceptability of the OR CEUSP 233U waste stream for near-surface disposal by evaluating long-term site stability and security, by performing extended (i.e., 10,000 and 60,000 y) modeling analyses, and by evaluating the effect of containers and the depth of burial on performance. Tier I results indicate that there is a reasonable expectation of compliance with all performance objectives if the OR CEUSP 233U waste stream is disposed in the Area 5 RWMS SLB disposal units. The maximum mean and 95th percentile PA results are all less than the performance objective for 1,000 y. Monte Carlo uncertainty analysis indicates that there is a high likelihood of compliance with all performance objectives. Tier II results indicate that the long-term performance of the OR CEUSP 233U waste stream is protective of human health and the environment. The Area 5 RWMS is located in one of the least populated and most arid regions of the U.S. Site characterization data indicate that infiltration of precipitation below the plant root zone at 2.5 meters (8.2 feet) ceased 10,000 to 15,000 y ago. The site is not expected to have a groundwater pathway as long as the current arid climate persists. The national security mission of the NNSS and the location of the Area 5 RWMS within the Frenchman Flat Corrective Action Unit require that access controls and land use restrictions be maintained indefinitely. PA modeling results for 10,000 to 60,000 y also indicate that the OR CEUSP 233U waste stream is acceptable for near-surface disposal. The mean resident air pathway annual total effective dose (TED), the resident all-pathways annual TED, and the acute drilling TED are less than their performance objectives for 10,000 y after closure. The mean radon-222 (222Rn) flux density exceeds the performance objective at 4,200 y, but this is due to waste already disposed at the Area 5 RWMS and is only slightly affected by disposal of the CEUSP 233U. The peak resident all-pathways annual TED from CEUSP key radionuclides occurs at 48,000 y and is less than the 0.25 millisievert performance objective. Disposal of the OR CEUSP 233U waste stream in a typical SLB trench slightly increases PA results. Increasing the depth was found to eliminate any impacts of the OR CEUSP 233U waste stream. Containers could not be shown to have any significant impact on performance due to the long half-life of the waste stream and a lack of data for pitting corrosion rates of stainless steel in soil. The results of the SA indicate that all performance objectives can be met with disposal of the OR CEUSP 233U waste stream in the SLB units at the Area 5 RWMS. The long-term performance of the OR CEUSP 233U waste stream disposed in the near surface is protective of human health

NSTec Environmental Management

2013-01-31T23:59:59.000Z

56

Uranium industry annual 1996  

SciTech Connect (OSTI)

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

NONE

1997-04-01T23:59:59.000Z

57

Process for reducing beta activity in uranium  

DOE Patents [OSTI]

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

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

1986-01-01T23:59:59.000Z

58

Process for reducing beta activity in uranium  

DOE Patents [OSTI]

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

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

1985-04-11T23:59:59.000Z

59

Uranium Industry Annual, 1992  

SciTech Connect (OSTI)

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

Not Available

1993-10-28T23:59:59.000Z

60

Extraction processes and solvents for recovery of cesium, strontium, rare earth elements, technetium and actinides from liquid radioactive waste  

DOE Patents [OSTI]

Cesium and strontium are extracted from aqueous acidic radioactive waste containing rare earth elements, technetium and actinides, by contacting the waste with a composition of a complex organoboron compound and polyethylene glycol in an organofluorine diluent mixture. In a preferred embodiment the complex organoboron compound is chlorinated cobalt dicarbollide, the polyethylene glycol has the formula RC.sub.6 H.sub.4 (OCH.sub.2 CH.sub.2).sub.n OH, and the organofluorine diluent is a mixture of bis-tetrafluoropropyl ether of diethylene glycol with at least one of bis-tetrafluoropropyl ether of ethylene glycol and bis-tetrafluoropropyl formal. The rare earths, technetium and the actinides (especially uranium, plutonium and americium), are extracted from the aqueous phase using a phosphine oxide in a hydrocarbon diluent, and reextracted from the resulting organic phase into an aqueous phase by using a suitable strip reagent.

Zaitsev, Boris N. (St. Petersburg, RU); Esimantovskiy, Vyacheslav M. (St. Petersburg, RU); Lazarev, Leonard N. (St. Petersburg, RU); Dzekun, Evgeniy G. (Ozersk, RU); Romanovskiy, Valeriy N. (St. Petersburg, RU); Todd, Terry A. (Aberdeen, ID); Brewer, Ken N. (Arco, ID); Herbst, Ronald S. (Idaho Falls, ID); Law, Jack D. (Pocatello, ID)

2001-01-01T23:59:59.000Z

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


61

Paragenesis and Geochronology of the Nopal I Uranium Deposit, Mexico  

SciTech Connect (OSTI)

Uranium deposits can, by analogy, provide important information on the long-term performance of radioactive waste forms and radioactive waste repositories. Their complex mineralogy and variable elemental and isotopic compositions can provide important information, provided that analyses are obtained on the scale of several micrometers. Here, we present a structural model of the Nopal I deposit as well as petrography at the nanoscale coupled with preliminary U-Th-Pb ages and O isotopic compositions of uranium-rich minerals obtained by Secondary Ion Mass Spectrometry (SIMS). This multi-technique approach promises to provide ''natural system'' data on the corrosion rate of uraninite, the natural analogue of spent nuclear fuel.

M. Fayek; M. Ren

2007-02-14T23:59:59.000Z

62

Depleted uranium: A DOE management guide  

SciTech Connect (OSTI)

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

NONE

1995-10-01T23:59:59.000Z

63

Uranium industry annual 1994  

SciTech Connect (OSTI)

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

NONE

1995-07-05T23:59:59.000Z

64

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

SciTech Connect (OSTI)

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

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

1993-12-31T23:59:59.000Z

65

Bugs boost Cold War clean-up: Bacteria could scrub uranium from sites contaminated decades ago. updated at midnight GMTtoday is friday, november 14  

E-Print Network [OSTI]

2003 · Fungus catches radioactive fallout 8 May 2002 · Depleted uranium soils battlefields 12 MarchBugs boost Cold War clean-up: Bacteria could scrub uranium from sites contaminated decades ago boost Cold War clean-up Bacteria could scrub uranium from sites contaminated decades ago. 13 October

Lovley, Derek

66

Uranium- and thorium-bearing pegmatites of the United States  

SciTech Connect (OSTI)

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.

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

1980-04-01T23:59:59.000Z

67

Final Uranium Leasing Program Programmatic Environmental Impact...  

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

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

68

Depleted Uranium Technical Brief  

E-Print Network [OSTI]

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

69

Uranium series disequilibrium in the Bargmann property area of Karnes County, Texas  

SciTech Connect (OSTI)

Historical evidence is presented for natural uranium series radioactive disequilibrium in uranium bearing soils in the Bargmann property area of karnes County on the Gulf Coastal Plain of south Texas. The early history of uranium exploration in the area is recounted and records of disequilibrium before milling and mining operations began are given. The property contains an open pit uranium mine associated with a larger ore body. In 1995, the US Department of Energy (DOE) directed Oak Ridge National Laboratory (ORNL) to evaluate the Bargmann tract for the presence of uranium mill tailings (ORNL 1996). There was a possibility that mill tailings had washed onto or blown onto the property from the former tailings piles in quantities that would warrant remediation under the Uranium Mill Tailings Remediation Action Project. Activity ratios illustrating disequilibrium between {sup 226}Ra and {sup 238}U in background soils during 1986 are listed and discussed. Derivations of uranium mass-to-activity conversion factors are covered in detail.

Davidson, J.R.

1998-02-01T23:59:59.000Z

70

Method for converting uranium oxides to uranium metal  

DOE Patents [OSTI]

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

Duerksen, Walter K. (Norris, TN)

1988-01-01T23:59:59.000Z

71

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

E-Print Network [OSTI]

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

Hart, Gus

72

Uranium Mill Tailings Remedial Action Project, Surface Project Management Plan. Revision 1  

SciTech Connect (OSTI)

Title I of the Uranium Mill Tailings Radiation Control Act (UMTRCA) authorizes the US Department of Energy (DOE) to undertake remedial action at 24 designated inactive uranium processing sites and associated vicinity properties (VP) containing uranium mill tailings and related residual radioactive materials. The purpose of the Uranium Mill Tailings Remedial Action (UMTRA) Surface Project is to minimize or eliminate radiation health hazards to the public and the environment at the 24 sites and related VPs. This document describes the management organization, system, and methods used to manage the design, construction, and other activities required to clean up the designated sites and associated VPs, in accordance with the UMTRCA.

Not Available

1994-12-01T23:59:59.000Z

73

Welding of uranium and uranium alloys  

SciTech Connect (OSTI)

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

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

1982-03-26T23:59:59.000Z

74

EIS-0132: Remedial Actions at the Former Union Carbide Corp. Uranium Mill Sites, Rifle, Garfield County, Colorado  

Broader source: Energy.gov [DOE]

The U.S. Department of Energy developed this statement to evaluate and compare the environmental impacts of remediating the residual radioactive materials left at the inactive uranium tailing sites in Rifle, Colorado.

75

EPA Update: NESHAP Uranium Activities  

E-Print Network [OSTI]

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

76

Uranium hexafluoride public risk  

SciTech Connect (OSTI)

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

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

1994-08-01T23:59:59.000Z

77

Process for continuous production of metallic uranium and uranium alloys  

DOE Patents [OSTI]

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

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

1995-06-06T23:59:59.000Z

78

Process for continuous production of metallic uranium and uranium alloys  

DOE Patents [OSTI]

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

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

1995-01-01T23:59:59.000Z

79

Radioactive Material Transportation Practices  

Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

Establishes standard transportation practices for Departmental programs to use in planning and executing offsite shipments of radioactive materials including radioactive waste. Does not cancel other directives.

2002-09-23T23:59:59.000Z

80

Radioactive Waste Management  

Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

To establish policies and guidelines by which the Department of Energy (DOE) manages tis radioactive waste, waste byproducts, and radioactively contaminated surplus facilities.

1984-02-06T23:59:59.000Z

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


81

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

E-Print Network [OSTI]

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

Winfree, Erik

82

Fernald vacuum transfer system for uranium materials repackaging  

SciTech Connect (OSTI)

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

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

2002-02-24T23:59:59.000Z

83

Uranium industry annual 1993  

SciTech Connect (OSTI)

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

Not Available

1994-09-01T23:59:59.000Z

84

Uranium Mill Tailings Remedial Action (UMTRA) Project. [UMTRA project  

SciTech Connect (OSTI)

The mission of the Uranium Mill Tailings Remedial Action (UMTRA) Project is explicitly stated and directed in the Uranium Mill Tailings Radiation Control Act of 1978, hereinafter referred to as the Act.'' Title I of the Act authorizes the Department of Energy (DOE) to undertake remedial action at designated inactive uranium processing sites (Attachment 1 and 2) and associated vicinity properties containing uranium mill tailings and other residual radioactive materials derived from the processing site. The purpose of the remedial actions is to stabilize and control such uranium mill tailings and other residual radioactive materials in a safe and environmentally sound manner to minimize radiation health hazards to the public. The principal health hazards and environmental concerns are: the inhalation of air particulates contaminated as a result of the emanation of radon from the tailings piles and the subsequent decay of radon daughters; and the contamination of surface and groundwaters with radionuclides or other chemically toxic materials. This UMTRA Project Plan identifies the mission and objectives of the project, outlines the technical and managerial approach for achieving them, and summarizes the performance, cost, and schedule baselines which have been established to guide operational activity. Estimated cost increases by 15 percent, or if the schedule slips by six months. 4 refs.

Not Available

1989-09-01T23:59:59.000Z

85

CHARACTERIZATION OF URANIUM, URANIUM OXIDE AND SILICON MULTILAYER THIN FILMS  

E-Print Network [OSTI]

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

Hart, Gus

86

Uranium dioxide electrolysis  

DOE Patents [OSTI]

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

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

2009-12-29T23:59:59.000Z

87

Pis'ma v ZhETF, vol.91, iss.9, pp.532{535 c 2010 May 10 First-principles investigation of uranium monochalcogenides  

E-Print Network [OSTI]

Pis'ma v ZhETF, vol.91, iss.9, pp.532{535 c 2010 May 10 First-principles investigation of uranium of the electronic structure and magnetic properties of uranium monochalcogenides: US, USe, UTe. The calculations. The electronic con guration 5f3 was found for all uranium compounds under investigation. Local Spin Density

Medvedeva, Julia E.

88

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

SciTech Connect (OSTI)

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

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

2013-01-01T23:59:59.000Z

89

WISE Uranium Project - Fact Sheet  

E-Print Network [OSTI]

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

Hazards From Depleted

90

India's Worsening Uranium Shortage  

SciTech Connect (OSTI)

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

Curtis, Michael M.

2007-01-15T23:59:59.000Z

91

U.S. Environmental Protection Agency Evaluation of Uranium Mining TENORM Wastes-Characteristics, Occurrence, and Risks  

SciTech Connect (OSTI)

The U.S. Environmental Protection Agency is completing a multi year effort to issue technical reports and obtain stakeholder views on future programs to mitigate potential hazards associated with uranium mining Technologically Enhanced Naturally Occurring Radioactive Materials (TENORM). The technical reports are the most comprehensive issued by the Agency on this topic, and should have utility for reclamation of abandoned uranium mines, as well as providing information for new mines proposed by the uranium mining industry. This presentation will provide principal results of the three technical reports issued, and elements of the proposed EPA program for uranium mining TENORM. (authors)

Setlow, L.W. [U.S. Environmental Protection Agency, Office of Radiation and Indoor Air (6608J), Washington, DC (United States); Peake, R.T. [U.S. Environmental Protection Agency, Office of Radiation and Indoor Air (6608J), Washington, DC (United States)

2007-07-01T23:59:59.000Z

92

Depleted uranium management alternatives  

SciTech Connect (OSTI)

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

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

1994-08-01T23:59:59.000Z

93

CHAPTER 5-RADIOACTIVE WASTE MANAGEMENT  

SciTech Connect (OSTI)

The ore pitchblende was discovered in the 1750's near Joachimstal in what is now the Czech Republic. Used as a colorant in glazes, uranium was identified in 1789 as the active ingredient by chemist Martin Klaproth. In 1896, French physicist Henri Becquerel studied uranium minerals as part of his investigations into the phenomenon of fluorescence. He discovered a strange energy emanating from the material which he dubbed 'rayons uranique.' Unable to explain the origins of this energy, he set the problem aside. About two years later, a young Polish graduate student was looking for a project for her dissertation. Marie Sklodowska Curie, working with her husband Pierre, picked up on Becquerel's work and, in the course of seeking out more information on uranium, discovered two new elements (polonium and radium) which exhibited the same phenomenon, but were even more powerful. The Curies recognized the energy, which they now called 'radioactivity,' as something very new, requiring a new interpretation, new science. This discovery led to what some view as the 'golden age of nuclear science' (1895-1945) when countries throughout Europe devoted large resources to understand the properties and potential of this material. By World War II, the potential to harness this energy for a destructive device had been recognized and by 1939, Otto Hahn and Fritz Strassman showed that fission not only released a lot of energy but that it also released additional neutrons which could cause fission in other uranium nuclei leading to a self-sustaining chain reaction and an enormous release of energy. This suggestion was soon confirmed experimentally by other scientists and the race to develop an atomic bomb was on. The rest of the development history which lead to the bombing of Hiroshima and Nagasaki in 1945 is well chronicled. After World War II, development of more powerful weapons systems by the United States and the Soviet Union continued to advance nuclear science. It was this defense application that formed the basis for the commercial nuclear power industry.

Marra, J.

2010-05-05T23:59:59.000Z

94

Flowsheets and source terms for radioactive waste projections  

SciTech Connect (OSTI)

Flowsheets and source terms used to generate radioactive waste projections in the Integrated Data Base (IDB) Program are given. Volumes of each waste type generated per unit product throughput have been determined for the following facilities: uranium mining, UF/sub 6/ conversion, uranium enrichment, fuel fabrication, boiling-water reactors (BWRs), pressurized-water reactors (PWRs), and fuel reprocessing. Source terms for DOE/defense wastes have been developed. Expected wastes from typical decommissioning operations for each facility type have been determined. All wastes are also characterized by isotopic composition at time of generation and by general chemical composition. 70 references, 21 figures, 53 tables.

Forsberg, C.W. (comp.)

1985-03-01T23:59:59.000Z

95

Method for the recovery of uranium values from uranium tetrafluoride  

DOE Patents [OSTI]

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

Kreuzmann, Alvin B. (Cincinnati, OH)

1983-01-01T23:59:59.000Z

96

Method for the recovery of uranium values from uranium tetrafluoride  

DOE Patents [OSTI]

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

Kreuzmann, A.B.

1982-10-27T23:59:59.000Z

97

Method for monitoring stack gases for uranium activity  

DOE Patents [OSTI]

A method for monitoring the stack gases of a purge cascade of a gaseous diffusion plant for uranium activity. A sample stream is taken from the stack gases and contacted with a volume of moisture-laden air for converting trace levels of uranium hexafluoride, if any, in the stack gases into particulate uranyl fluoride. A continuous strip of filter paper from a supply roll is passed through this sampling stream to intercept and gather any uranyl fluoride in the sampling stream. This filter paper is then passed by an alpha scintillation counting device where any radioactivity on the filter paper is sensed so as to provide a continuous monitoring of the gas stream for activity indicative of the uranium content in the stack gases.

Beverly, Claude R. (Paducah, KY); Ernstberger, Harold G. (Paducah, KY)

1988-01-01T23:59:59.000Z

98

Total effective dose equivalent associated with fixed uranium surface contamination  

SciTech Connect (OSTI)

This report provides the technical basis for establishing a uranium fixed-contamination action level, a fixed uranium surface contamination level exceeding the total radioactivity values of Appendix D of Title 10, Code of Federal Regulations, part 835 (10CFR835), but below which the monitoring, posting, and control requirements for Radiological Areas are not required for the area of the contamination. An area of fixed uranium contamination between 1,000 dpm/100 cm{sup 2} and that level corresponding to an annual total effective dose equivalent (TEDE) of 100 mrem requires only routine monitoring, posting to alert personnel of the contamination, and administrative control. The more extensive requirements for monitoring, posting, and control designated by 10CFR835 for Radiological Areas do not have to be applied for these intermediate fixed-contamination levels.

Bogard, J.S.; Hamm, R.N.; Ashley, J.C.; Turner, J.E.; England, C.A.; Swenson, D.E.; Brown, K.S.

1997-04-01T23:59:59.000Z

99

Method for monitoring stack gases for uranium activity  

DOE Patents [OSTI]

A method for monitoring the stack gases of a purge cascade of gaseous diffusion plant for uranium activity. A sample stream is taken from the stack gases and contacted with a volume of moisture-laden air for converting trace levels of uranium hexafluoride, if any, in the stack gases into particulate uranyl fluoride. A continuous strip of filter paper from a supply roll is passed through this sampling stream to intercept and gather any uranyl fluoride in the sampling stream. This filter paper is then passed by an alpha scintillation counting device where any radioactivity on the filter paper is sensed so as to provide a continuous monitoring of the gas stream for activity indicative of the uranium content in the stack gases. 1 fig.

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

1985-07-03T23:59:59.000Z

100

Proceedings of Workshop on Uranium Production Environmental Restoration: An exchange between the United States and Germany  

SciTech Connect (OSTI)

Scientists, engineers, elected officials, and industry regulators from the United, States and Germany met in Albuquerque, New Mexico, August 16--20, 1993, in the first joint international workshop to discuss uranium tailings remediation. Entitled ``Workshop on Uranium Production Environmental Restoration: An Exchange between the US and Germany,`` the meeting was hosted by the US Department of Energy`s (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project. The goal of the workshop was to further understanding and communication on the uranium tailings cleanup projects in the US and Germany. Many communities around the world are faced with an environmental legacy -- enormous quantities of hazardous and low-level radioactive materials from the production of uranium used for energy and nuclear weapons. In 1978, the US Congress passed the Uranium Mill Tailings Radiation Control Act. Title I of the law established a program to assess the tailings at inactive uranium processing sites and provide a means for joint federal and state funding of the cleanup efforts at sites where all or substantially all of the uranium was produced for sale to a federal agency. The UMTRA Project is responsible for the cleanup of 24 sites in 10 states. Germany is facing nearly identical uranium cleanup problems and has established a cleanup project. At the workshop, participants had an opportunity to interact with a broad cross section of the environmental restoration and waste disposal community, discuss common concerns and problems, and develop a broader understanding of the issues. Abstracts are catalogued individually for the data base.

Not Available

1993-12-31T23:59:59.000Z

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


101

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

DOE Patents [OSTI]

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

Herrmann, Steven Douglas

2014-05-27T23:59:59.000Z

102

Bioremediation of ground water contaminants at a uranium mill tailings site  

SciTech Connect (OSTI)

Ground water contaminated with uranium from milling operations must be remediated to reduce the migration of soluble toxic compounds. At the mill tailings site near Tuba City, Arizona (USA) the approach is to employ bioremediation for in situ immobilization of uranium by bacterial reduction of uranyl, U(VI), compounds to uraninite, U(IV). In this initial phase of remediation, details are provided to indicate the magnitude of the contamination problem and to present preliminary evidence supporting the proposition that bacterial immobilization of uranium is possible. Additionally, consideration is given to contaminating cations and anions that may be at toxic levels in ground water at this uranium mill tailing site and detoxification strategies using bacteria are addressed. A model concept is employed so that results obtained at the Tuba City site could contribute to bioremediation of ground water at other uranium mill tailings sites.

Barton, L.L.; Nuttall, H.E.; Thomson, B.M.; Lutze, W. [Univ. of New Mexico, Albuquerque, NM (United States)

1995-12-31T23:59:59.000Z

103

Radioactive Waste Management (Minnesota)  

Broader source: Energy.gov [DOE]

This section regulates the transportation and disposal of high-level radioactive waste in Minnesota, and establishes a Nuclear Waste Council to monitor the federal high-level radioactive waste...

104

Uranium Enrichment Decontamination and Decommissioning Fund's...  

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

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

105

Radioactive Materials License Commitments  

E-Print Network [OSTI]

Radioactive Materials License Commitments for The University of Texas at Austin May 2009 July 2009 in the use of radioactive materials. In July 1963, the State of Texas granted The University of Texas at Austin a broad radioactive materials license for research, development and instruction. While this means

106

Engineering assessment of inactive uranium mill tailings  

SciTech Connect (OSTI)

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

Not Available

1981-07-01T23:59:59.000Z

107

Process for electrolytically preparing uranium metal  

DOE Patents [OSTI]

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

Haas, Paul A. (Knoxville, TN)

1989-01-01T23:59:59.000Z

108

Controlling uranium reactivity March 18, 2008  

E-Print Network [OSTI]

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

Meyer, Karsten

109

Influence of uranium hydride oxidation on uranium metal behaviour  

SciTech Connect (OSTI)

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

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

2013-07-01T23:59:59.000Z

110

Uranium-titanium-niobium alloy  

DOE Patents [OSTI]

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

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

1990-01-01T23:59:59.000Z

111

Uranium deposits of Brazil  

SciTech Connect (OSTI)

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

NONE

1991-09-01T23:59:59.000Z

112

Uranium hexafluoride handling. Proceedings  

SciTech Connect (OSTI)

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

Not Available

1991-12-31T23:59:59.000Z

113

Polybenzimidazole compounds  

DOE Patents [OSTI]

A PBI compound includes imidazole nitrogens at least a portion of which are substituted with a moiety containing a carbonyl group, the substituted imidazole nitrogens being bonded to carbon of the carbonyl group. At least 85% of the nitrogens may be substituted. The carbonyl-containing moiety may include RCO--, where R is alkoxy or haloalkyl. The PBI compound may exhibit a first temperature marking an onset of weight loss corresponding to reversion of the substituted PBI that is less than a second temperature marking an onset of decomposition of an otherwise identical PBI compound without the substituted moiety. The PBI compound may be included in separatory media. A substituted PBI synthesis method may include providing a parent PBI in a less than 5 wt % solvent solution. Substituting may use more than 5 equivalents in relation to the imidazole nitrogens to be substituted.

Klaehn, John R. (Idaho Falls, ID); Peterson, Eric S. (Idaho Falls, ID); Orme, Christopher J. (Shelley, ID); Jones, Michael G. (Chubbuck, ID); Wertsching, Alan K. (Idaho Falls, ID); Luther, Thomas A. (Idaho Falls, ID); Trowbridge, Tammy L. (Idaho Falls, ID)

2011-11-22T23:59:59.000Z

114

Polybenzimidazole compounds  

DOE Patents [OSTI]

A PBI compound that includes imidazole nitrogens, at least a portion of which are substituted with an organic-inorganic hybrid moiety. At least 85% of the imidazole nitrogens may be substituted. The organic-inorganic hybrid moiety may be an organosilane moiety, for example, (R)Me.sub.2SiCH.sub.2--, where R is selected from among methyl, phenyl, vinyl, and allyl. The PBI compound may exhibit similar thermal properties in comparison to the unsubstituted PBI. The PBI compound may exhibit a solubility in an organic solvent greater than the solubility of the unsubstituted PBI. The PBI compound may be included in separatory media. A substituted PBI synthesis method may include providing a parent PBI in a less than 5 wt % solvent solution. Substituting may occur at about room temperature and/or at about atmospheric pressure. Substituting may use at least five equivalents in relation to the imidazole nitrogens to be substituted or, preferably, about fifteen equivalents.

Klaehn, John R. (Idaho Falls, ID); Peterson, Eric S. (Idaho Falls, ID); Wertsching, Alan K. (Idaho Falls, ID); Orme, Christopher J. (Shelley, ID); Luther, Thomas A. (Idaho Falls, ID); Jones, Michael G. (Pocatello, ID)

2010-08-10T23:59:59.000Z

115

DISSOLVED CONCENTRATION LIMITS OF RADIOACTIVE ELEMENTS  

SciTech Connect (OSTI)

The purpose of this study is to evaluate dissolved concentration limits (also referred to as solubility limits) of elements with radioactive isotopes under probable repository conditions, based on geochemical modeling calculations using geochemical modeling tools, thermodynamic databases, field measurements, and laboratory experiments. The scope of this modeling activity is to predict dissolved concentrations or solubility limits for 14 elements with radioactive isotopes (actinium, americium, carbon, cesium, iodine, lead, neptunium, plutonium, protactinium, radium, strontium, technetium, thorium, and uranium) important to calculated dose. Model outputs for uranium, plutonium, neptunium, thorium, americium, and protactinium are in the form of tabulated functions with pH and log (line integral) CO{sub 2} as independent variables, plus one or more uncertainty terms. The solubility limits for the remaining elements are either in the form of distributions or single values. The output data from this report are fundamental inputs for Total System Performance Assessment for the License Application (TSPA-LA) to determine the estimated release of these elements from waste packages and the engineered barrier system. Consistent modeling approaches and environmental conditions were used to develop solubility models for all of the actinides. These models cover broad ranges of environmental conditions so that they are applicable to both waste packages and the invert. Uncertainties from thermodynamic data, water chemistry, temperature variation, and activity coefficients have been quantified or otherwise addressed.

NA

2004-11-22T23:59:59.000Z

116

Uranium immobilization and nuclear waste  

SciTech Connect (OSTI)

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

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

1982-02-01T23:59:59.000Z

117

Radioactive and chemotoxic wastes: Only radioactive wastes?  

SciTech Connect (OSTI)

Radioactive waste arising from Italian Nuclear Power Plants and Research Centers, classified as 1st and 2nd Category wastes, are managed only as radioactive wastes following the Technical Guide No. 26 issued by the Italian Regulatory Body: ENEA DISP on 1987. A very important Regulatory Regime revision for Italian Nuclear Activities started at the end of 1991. This paper considers the need to develop a new strategy dedicated to mixed waste in line with current international trends.

Eletti, G.F.; Tocci, M. [ENEA DISP, Rome (Italy)

1993-12-31T23:59:59.000Z

118

Corrosion-resistant uranium  

DOE Patents [OSTI]

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

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

1981-10-21T23:59:59.000Z

119

Corrosion-resistant uranium  

DOE Patents [OSTI]

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

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

1983-01-01T23:59:59.000Z

120

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

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


121

Evaluation of Uranium Measurements in Water by Various Methods - 13571  

SciTech Connect (OSTI)

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

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

2013-07-01T23:59:59.000Z

122

Brazilian uranium mine decommissioning-chemical and radiological study of waste rock piles  

SciTech Connect (OSTI)

The Pocos de Caldas plateau is a high-natural-radioactivity area in the state of Minas Gerais, southeast Brazil. Uranium occurrence in the plateau was first observed in 1948. Mining started in 1977 with mine scouring, and the first ore pile was constructed in 1981. Waste rocks are derived from the mine material. The analysis of core samples is discussed.

Wiikmann, L. O. [Industrias Nucleares do Brasil, Pocos de Caldas (Brazil)

1996-12-31T23:59:59.000Z

123

Science Blog -Bacterium cleans up uranium, generates electricity Create an account  

E-Print Network [OSTI]

Science Blog - Bacterium cleans up uranium, generates electricity Create an account :: Home electricity Department of Energy-funded researchers have decoded and analyzed the genome of a bacterium with the potential to bioremediate radioactive metals and generate electricity. In an article published

Lovley, Derek

124

Radioactive Waste: 1. Radioactive waste from your lab is  

E-Print Network [OSTI]

Radioactive Waste: 1. Radioactive waste from your lab is collected by the RSO. 2. Dry radioactive waste must be segregated by isotope. 3. Liquid radioactive waste must be separated by isotope. 4. Liquid frequently and change them if contaminated. 5. Use radioactive waste container to collect the waste. 6. Check

Jia, Songtao

125

Radioactive Waste Management in Central Asia - 12034  

SciTech Connect (OSTI)

After the collapse of the Soviet Union the newly independent states in Central Asia (CA) whose regulatory bodies were set up recently are facing problems with the proper management of radioactive waste and so called 'nuclear legacy' inherited from the past activities. During the former Soviet Union (SU) period, various aspects of nuclear energy use took place in CA republics of Kazakhstan, Kyrgyzstan, Tajikistan and Uzbekistan. Activities range from peaceful use of energy to nuclear testing for example at the former Semipalatinsk Nuclear Test Site (SNTS) in Kazakhstan, and uranium mining and milling industries in all four countries. Large amounts of radioactive waste (RW) have been accumulated in Central Asia and are waiting for its safe disposal. In 2008 the Norwegian Radiation Protection Authority (NRPA), with the support of the Norwegian Ministry of Foreign Affairs, has developed bilateral projects that aim to assist the regulatory bodies in Kazakhstan, Kyrgyzstan Tajikistan, and Uzbekistan (from 2010) to identify and draft relevant regulatory requirements to ensure the protection of the personnel, population and environment during the planning and execution of remedial actions for past practices and radioactive waste management in the CA countries. The participating regulatory authorities included: Kazakhstan Atomic Energy Agency, Kyrgyzstan State Agency on Environmental Protection and Forestry, Nuclear Safety Agency of Tajikistan, and State Inspectorate on Safety in Industry and Mining of Uzbekistan. The scope of the projects is to ensure that activities related to radioactive waste management in both planned and existing exposure situations in CA will be carried out in accordance with the international guidance and recommendations, taking into account the relevant regulatory practice from other countries in this area. In order to understand the problems in the field of radioactive waste management we have analysed the existing regulations through the so called 'Threat assessment' in each CA country which revealed additional problems in the existing regulatory documents beyond those described at the start of our ongoing bilateral projects in Kazakhstan, Kirgizistan Tajikistan and Uzbekistan. (authors)

Zhunussova, Tamara; Sneve, Malgorzata; Liland, Astrid [Norwegian Radiation Protection Authority (Norway)

2012-07-01T23:59:59.000Z

126

Radioactive Waste Management Basis  

SciTech Connect (OSTI)

The purpose of this Radioactive Waste Management Basis is to describe the systematic approach for planning, executing, and evaluating the management of radioactive waste at LLNL. The implementation of this document will ensure that waste management activities at LLNL are conducted in compliance with the requirements of DOE Order 435.1, Radioactive Waste Management, and the Implementation Guide for DOE Manual 435.1-1, Radioactive Waste Management Manual. Technical justification is provided where methods for meeting the requirements of DOE Order 435.1 deviate from the DOE Manual 435.1-1 and Implementation Guide.

Perkins, B K

2009-06-03T23:59:59.000Z

127

Radioactivity in Food and the Environment, 2005  

E-Print Network [OSTI]

.............................................................................................. 0 .. Radioactive waste disposal from nuclear sites ........................................................................................................................... 9 . Disposals of radioactive waste............................................ .. Radioactive waste disposal at sea

128

Molten uranium dioxide structure and dynamics  

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

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

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

2014-11-20T23:59:59.000Z

129

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

E-Print Network [OSTI]

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

Igor Iosilevskiy; Victor Gryaznov

2010-05-23T23:59:59.000Z

130

Method of preparation of uranium nitride  

DOE Patents [OSTI]

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

Kiplinger, Jaqueline Loetsch; Thomson, Robert Kenneth James

2013-07-09T23:59:59.000Z

131

URANIUM MILLING ACTIVITIES AT SEQUOYAH FUELS CORPORATION  

E-Print Network [OSTI]

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

unknown authors

132

Interaction of Uranium(VI) with Phthalic Acid  

SciTech Connect (OSTI)

Phthalic acid, a ubiquitous organic compound found in soil, water, and in domestic and nuclear wastes can affect the mobility and bioavailability of metals and radionuclides. We examined the complexation of uranium with phthalic acid by potentiometric titration, electrospray ionization-mass spectroscopy (ESI-MS), and extended X-ray absorption fine structure (EXAFS) analysis. Potentiometric titration of a 1:1 U/phthalic acid indicated uranyl ion bonding with both carboxylate groups of phthalic acid; above pH 5 the uranyl ion underwent hydrolysis with one hydroxyl group coordinated to the inner-sphere of uranium. In the presence of excess phthalic acid, ESI-MS analysis revealed the formation of both 1:1 and 1:2 U/phthalic acid complexes. EXAFS studies confirmed the mononuclear biligand 1:2 U/phthalic acid complex as the predominant form. These results show that phthalates can form soluble stable complexes with uranium and may affect its mobility.

Vazquez, G.; Dodge, C; Francis, A

2008-01-01T23:59:59.000Z

133

Depleted-Uranium Weapons the Whys and Wherefores  

E-Print Network [OSTI]

The only military application in which present-day depleted-uranium (DU) alloys out-perform tungsten alloys is long-rod penetration into a main battle-tank's armor. However, this advantage is only on the order of 10% and disappearing when the comparison is made in terms of actual lethality of complete anti-tank systems instead of laboratory-type steel penetration capability. Therefore, new micro- and nano-engineered tungsten alloys may soon out-perform existing DU alloys, enabling the production of tungsten munition which will be better than uranium munition, and whose overall life-cycle cost will be less due to the absence of the problems related to the radioactivity of uranium. The reasons why DU weapons have been introduced and used are analysed from the perspective that their radioactivity must have played an important role in the decision making process. It is found that DU weapons belong to the diffuse category of low-radiological-impact nuclear weapons to which emerging types of low-yield, i.e., fourth...

Gsponer, A

2003-01-01T23:59:59.000Z

134

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

SciTech Connect (OSTI)

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

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

2013-02-01T23:59:59.000Z

135

Radioactive waste disposal package  

DOE Patents [OSTI]

A radioactive waste disposal package comprising a canister for containing vitrified radioactive waste material and a sealed outer shell encapsulating the canister. A solid block of filler material is supported in said shell and convertible into a liquid state for flow into the space between the canister and outer shell and subsequently hardened to form a solid, impervious layer occupying such space.

Lampe, Robert F. (Bethel Park, PA)

1986-01-01T23:59:59.000Z

136

EIS-0084: Incineration Facility for Radioactively Contaminated PCBs and Other Wastes, Oak Ridge, Tennessee  

Broader source: Energy.gov [DOE]

The U.S. Department of Energy Office of Uranium Enrichment and Assessment prepared this statement to assess the environmental impacts of the construction and operation of the proposed Oak Ridge Gaseous Diffusion Plant, an incineration facility to dispose of radioactively contaminated polychlorinated biophenyls, as well as combustible waste from the Paducah, Portsmouth and Oak Ridge facilities.

137

Method for fabricating uranium foils and uranium alloy foils  

DOE Patents [OSTI]

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

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

2006-09-05T23:59:59.000Z

138

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

SciTech Connect (OSTI)

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

Sarychev, Michael; /Fermilab

2011-09-21T23:59:59.000Z

139

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

SciTech Connect (OSTI)

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

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

2003-08-01T23:59:59.000Z

140

ICPP radioactive liquid and calcine waste technologies evaluation. Interim report  

SciTech Connect (OSTI)

The Department of Energy (DOE) has received spent nuclear fuel (SNF) at the Idaho Chemical Processing Plant (ICPP) for interim storage since 1951 and reprocessing since 1953. Until recently, the major activity of the ICPP has been the reprocessing of SNF to recover fissile uranium; however, changing world events have raised questions concerning the need to recover and recycle this material. In April 1992, DOE chose to discontinue reprocessing SNF for uranium recovery and shifted its focus toward the management and disposition of radioactive wastes accumulated through reprocessing activities. Currently, 1.8 million gallons of radioactive liquid wastes (1.5 million gallons of radioactive sodium-bearing liquid wastes and 0.3 million gallons of high-level liquid waste) and 3,800 cubic meters (m{sup 3}) of calcine waste are in inventory at the ICPP. Legal drivers and agreements exist obligating the INEL to develop, demonstrate, and implement technologies for safe and environmentally sound treatment and interim storage of radioactive liquid and calcine waste. Candidate treatment processes and waste forms are being evaluated using the Technology Evaluation and Analysis Methodology (TEAM) Model. This process allows decision makers to (1) identify optimum radioactive waste treatment and disposal form alternatives; (2) assess tradeoffs between various optimization criteria; (3) identify uncertainties in performance parameters; and (4) focus development efforts on options that best satisfy stakeholder concerns. The Systems Analysis technology evaluation presented in this document supports the DOE in selecting the most effective radioactive liquid and calcine waste management plan to implement in compliance with established regulations, court orders, and agreements.

Murphy, J.A.; Pincock, L.F.; Christiansen, I.N.

1994-06-01T23:59:59.000Z

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


141

XAFS of Synthetic Iron(III)-Arsenate Co-Precipitates and Uranium Mill Neutralized Raffinate  

SciTech Connect (OSTI)

XAFS studies were carried out for chemical speciation of arsenic species in uranium mill neutralized raffinate solids. To aid the structural characterization, synthetic iron(III)-arsenate co-precipitates were prepared to mimic the actual uranium mill tailings neutralization products. The principle components analysis method was used to validate the synthetic amorphous scorodite as a primary model compound for arsenate species in the raffinate samples under the specific precipitation conditions.

Chen, N. [Canadian Light Source, University of Saskatchewan, Saskatoon, SK S7N 0X4 (Canada); Department of Geological Sciences, University of Saskatchewan, Saskatoon, SK (Canada); Jiang, D. T. [Canadian Light Source, University of Saskatchewan, Saskatoon, SK S7N 0X4 (Canada); COGEMA Resources Inc., Saskatoon, SK S7K 3X5 (Canada); Department of Physics, University of Guelph, Guelph, ON N1G 2W1 (Canada); Cutler, J. [Canadian Light Source, University of Saskatchewan, Saskatoon, SK S7N 0X4 (Canada); Demopoulos, G. P. [Department of Geological Sciences, University of Saskatchewan, Saskatoon, SK (Canada); Rowson, J. W. [Department of Materials Engineering, McGill University, Montreal, QC H3A 2B2 (Canada)

2007-02-02T23:59:59.000Z

142

RADIOACTIVE WASTE DISPOSAL IN GRANITE  

E-Print Network [OSTI]

RADIOACTIVE WASTE DISPOSAL IN GRANITE Paul A. WitherspoonRADIOACTIVE WASTE DISPOSAL IN GRANITE Paul A. Wither spoona repository site in granite are to evaluate the suitability

Witherspoon, P.A.

2010-01-01T23:59:59.000Z

143

Annual status report on the Uranium Mill Tailings Remedial Action Program  

SciTech Connect (OSTI)

This fourteenth annual status report for the Uranium Mill Tailings Remedial Action (UMTRA) Project Office summarizes activities of the Uranium Mill Tailings Remedial Action Surface (UMTRA-Surface) and Uranium Mill Tailings Remedial Action Groundwater (UMTRA-Groundwater) Projects undertaken during fiscal year (FY) 1992 by the US Department of Energy (DOE) and other agencies. Project goals for FY 1993 are also presented. An annual report of this type was a statutory requirement through January 1, 1986, pursuant to the Uranium Mill Tailings Radiation Control Act (UMTRCA) of 1978, Public Law (PL) 95-604. The DOE will continue to submit annual reports to DOE-Headquarters, the states, tribes, and local representatives through Project completion in order to inform the public of the yearly Project status. The purpose of the remedial action is to stabilize and control the tailings and other residual radioactive material (RRM) located on the inactive uranium processing sites in a safe and environmentally sound manner, and to minimize or eliminate potential health hazards. Commercial and residential properties near designated processing sites that are contaminated with material from the sites, herein referred to as ``vicinity properties (VP),`` are also eligible for remedial action. Included in the UMTRA Project are 24 inactive uranium processing sites and associated VPs located in 10 states, and the VPs associated with the Edgemont, South Dakota, uranium mill currently owned by the Tennessee Valley Authority (TVA) (Figure A.1, Appendix A).

Not Available

1992-12-01T23:59:59.000Z

144

Strongly correlated electron systems in uranium-based compounds  

E-Print Network [OSTI]

T (K) Figure 3.4: Electrical resistivity ? vs. temperature TT (K) Figure 3.5: Electrical resistivity ? vs. temperature TT (K) Figure 3.6: Electrical resistivity ? vs. temperature T

Kanchanavatee, Noravee

2012-01-01T23:59:59.000Z

145

LANL researchers improve path to producing uranium compounds, candidates  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc DocumentationP-SeriesFlickrinformationPostdocs &Jeff Yarbrough joins Los AlamosLANL

146

Uranium Mill Tailings Remedial Action Project 1993 Environmental Report  

SciTech Connect (OSTI)

This annual report documents the Uranium Mill Tailing Remedial Action (UMTRA) Project environmental monitoring and protection program. The UMTRA Project routinely monitors radiation, radioactive residual materials, and hazardous constituents at associated former uranium tailings processing sites and disposal sites. At the end of 1993, surface remedial action was complete at 10 of the 24 designated UMTRA Project processing sites. In 1993 the UMTRA Project office revised the UMTRA Project Environmental Protection Implementation Plan, as required by the US DOE. Because the UMTRA Project sites are in different stages of remedial action, the breadth of the UMTRA environmental protection program differs from site to site. In general, sites actively undergoing surface remedial action have the most comprehensive environmental programs for sampling media. At sites where surface remedial action is complete and at sites where remedial action has not yet begun, the environmental program consists primarily of surface water and ground water monitoring to support site characterization, baseline risk assessments, or disposal site performance assessments.

Not Available

1994-10-01T23:59:59.000Z

147

Standard specification for sintered (Uranium-Plutonium) dioxide pellets  

E-Print Network [OSTI]

1.1 This specification covers finished sintered and ground (uranium-plutonium) dioxide pellets for use in thermal reactors. It applies to uranium-plutonium dioxide pellets containing plutonium additions up to 15 % weight. This specification may not completely cover the requirements for pellets fabricated from weapons-derived plutonium. 1.2 This specification does not include (1) provisions for preventing criticality accidents or (2) requirements for health and safety. Observance of this specification does not relieve the user of the obligation to be aware of and conform to all applicable international, federal, state, and local regulations pertaining to possessing, processing, shipping, or using source or special nuclear material. Examples of U.S. government documents are Code of Federal Regulations Title 10, Part 50Domestic Licensing of Production and Utilization Facilities; Code of Federal Regulations Title 10, Part 71Packaging and Transportation of Radioactive Material; and Code of Federal Regulations Tit...

American Society for Testing and Materials. Philadelphia

2001-01-01T23:59:59.000Z

148

Radioactive Waste Management Manual  

Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

This Manual further describes the requirements and establishes specific responsibilities for implementing DOE O 435.1, Radioactive Waste Management, for the management of DOE high-level waste, transuranic waste, low-level waste, and the radioactive component of mixed waste. The purpose of the Manual is to catalog those procedural requirements and existing practices that ensure that all DOE elements and contractors continue to manage DOE's radioactive waste in a manner that is protective of worker and public health and safety, and the environment. Does not cancel other directives.

1999-07-09T23:59:59.000Z

149

Unexpected, Stable Form of Uranium Detected | EMSL  

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

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

150

Radioactive occurrences in veins and igneous and metamorphic rocks of New Mexico with annotated bibliography. [Over 600 citations  

SciTech Connect (OSTI)

From an extensive literature search and field examination of 96 nonsandstone radioactive occurrences, the author compiled an annotated bibliography of over 600 citations and a list of 327 radioactive occurrences in veins and igneous and metamorphic rocks of New Mexico. The citations are indexed by individual radioactive occurrence, geographic area, county, fluorspar deposits and occurrences, geochemical analyses, and geologic maps. In addition, the geology, mineralization, and uranium and thorium potential of 41 geographic areas in New Mexico containing known radioactive occurrences in veins and igneous and metamorphic rocks or that contain host rocks considered favorable for uranium or thorium mineralization are summarized. A list of aerial-radiometric, magnetic, hydrogeochemical, and stream-sediment survey reports is included.

McLemore, V. T.

1982-01-01T23:59:59.000Z

151

Dynamic radioactive particle source  

DOE Patents [OSTI]

A method and apparatus for providing a timed, synchronized dynamic alpha or beta particle source for testing the response of continuous air monitors (CAMs) for airborne alpha or beta emitters is provided. The method includes providing a radioactive source; placing the radioactive source inside the detection volume of a CAM; and introducing an alpha or beta-emitting isotope while the CAM is in a normal functioning mode.

Moore, Murray E.; Gauss, Adam Benjamin; Justus, Alan Lawrence

2012-06-26T23:59:59.000Z

152

Radioactive Waste Management Manual  

Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

This Manual further describes the requirements and establishes specific responsibilities for implementing DOE O 435.1, Radioactive Waste Management, for the management of DOE high-level waste, transuranic waste, low-level waste, and the radioactive component of mixed waste. Change 1 dated 6/19/01 removes the requirement that Headquarters is to be notified and the Office of Environment, Safety and Health consulted for exemptions for use of non-DOE treatment facilities. Certified 1-9-07.

1999-07-09T23:59:59.000Z

153

DISSOLVED CONCENTRATION LIMITS OF RADIOACTIVE ELEMENTS  

SciTech Connect (OSTI)

The purpose of this study is to evaluate dissolved concentration limits (also referred to as solubility limits) of elements with radioactive isotopes under probable repository conditions, based on geochemical modeling calculations using geochemical modeling tools, thermodynamic databases, field measurements, and laboratory experiments. The scope of this activity is to predict dissolved concentrations or solubility limits for elements with radioactive isotopes (actinium, americium, carbon, cesium, iodine, lead, neptunium, plutonium, protactinium, radium, strontium, technetium, thorium, and uranium) relevant to calculated dose. Model outputs for uranium, plutonium, neptunium, thorium, americium, and protactinium are provided in the form of tabulated functions with pH and log fCO{sub 2} as independent variables, plus one or more uncertainty terms. The solubility limits for the remaining elements are either in the form of distributions or single values. Even though selection of an appropriate set of radionuclides documented in Radionuclide Screening (BSC 2002 [DIRS 160059]) includes actinium, transport of Ac is not modeled in the total system performance assessment for the license application (TSPA-LA) model because of its extremely short half-life. Actinium dose is calculated in the TSPA-LA by assuming secular equilibrium with {sup 231}Pa (Section 6.10); therefore, Ac is not analyzed in this report. The output data from this report are fundamental inputs for TSPA-LA used to determine the estimated release of these elements from waste packages and the engineered barrier system. Consistent modeling approaches and environmental conditions were used to develop solubility models for the actinides discussed in this report. These models cover broad ranges of environmental conditions so they are applicable to both waste packages and the invert. Uncertainties from thermodynamic data, water chemistry, temperature variation, and activity coefficients have been quantified or otherwise addressed.

P. Bernot

2005-07-13T23:59:59.000Z

154

Uranium Mill Tailings Radiation Control Act of 1978  

SciTech Connect (OSTI)

The long-term environmental effects of the Uranium Mill Tailings Radiation Control Act of 1978 address the public health hazards of radioactive wastes and recognize the significance of this issue to public acceptance of nuclear energy. Title I of the Act deals with stabilizing and controlling mill tailings at inactive sites and classifies the sites by priority. It represents a major Federal commitment. Title II changes and strengthens Nuclear Regulatory Commission authority, but it will have little overall impact. It is not possible to assess the Act's effect because there is no way to know if current technology will be adequate for the length of time required. 76 references. (DCK)

Magee, J.

1980-01-01T23:59:59.000Z

155

2013 Domestic Uranium Production Report  

E-Print Network [OSTI]

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

156

Domestic Uranium Production Report  

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

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

157

Domestic Uranium Production Report  

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

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

158

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

159

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

160

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

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


161

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

162

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

163

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

164

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

165

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

166

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

167

Uranium Marketing Annual Report -  

Gasoline and Diesel Fuel Update (EIA)

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

168

Fingerprinting Uranium | EMSL  

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

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169

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

SciTech Connect (OSTI)

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

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

1995-09-01T23:59:59.000Z

170

Preserving Ultra-Pure Uranium-233  

SciTech Connect (OSTI)

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

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

2011-10-01T23:59:59.000Z

171

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

SciTech Connect (OSTI)

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

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

2000-09-01T23:59:59.000Z

172

APPENDIX J Partition Coefficients For Uranium  

E-Print Network [OSTI]

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

173

Uranium ore treatment. January 1970-May 1981 (citations from the Engineering Index Data Base). Report for Jan 70-May 81  

SciTech Connect (OSTI)

The treatment of uranium ores is presented with emphasis placed on acid leaching as the primary step in the process. Tailing disposal and proper handling of radioactive materials, including environmental monitoring is emphasized. Primary treatment procedures include ion exchange, sulfuric acid leaching, solvent extraction and sedimentation. (Contains 300 citations fully indexed and including a title list.)

Not Available

1981-05-01T23:59:59.000Z

174

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

Broader source: Energy.gov [DOE]

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

175

Integrated data base report--1996: US spent nuclear fuel and radioactive waste inventories, projections, and characteristics  

SciTech Connect (OSTI)

The Integrated Data Base Program has compiled historic data on inventories and characteristics of both commercial and U.S. Department of Energy (DOE) spent nuclear fuel (SNF) and commercial and U.S. government-owned radioactive wastes. Inventories of most of these materials are reported as of the end of fiscal year (FY) 1996, which is September 30, 1996. Commercial SNF and commercial uranium mill tailings inventories are reported on an end-of-calendar year (CY) basis. All SNF and radioactive waste data reported are based on the most reliable information available from government sources, the open literature, technical reports, and direct contacts. The information forecasted is consistent with the latest DOE/Energy Information Administration (EIA) projections of U.S. commercial nuclear power growth and the expected DOE-related and private industrial and institutional activities. The radioactive materials considered, on a chapter-by-chapter basis, are SNF, high-level waste, transuranic waste, low-level waste, uranium mill tailings, DOE Environmental Restoration Program contaminated environmental media, naturally occurring and accelerator-produced radioactive material, and mixed (hazardous and radioactive) low-level waste. For most of these categories, current and projected inventories are given through FY 2030, and the radioactivity and thermal power are calculated based on reported or estimated isotopic compositions.

NONE

1997-12-01T23:59:59.000Z

176

Operating limit evaluation for disposal of uranium enrichment plant wastes  

SciTech Connect (OSTI)

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

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

1996-02-01T23:59:59.000Z

177

The End of Cheap Uranium  

E-Print Network [OSTI]

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

Michael Dittmar

2011-06-21T23:59:59.000Z

178

Annual status report on the Uranium Mill Tailings Remedial Action Program  

SciTech Connect (OSTI)

This eleventh annual status report summarizes activities of the Uranium Mill Tailings Remedial Action (UMTRA) Project undertaken during Fiscal Year (FY) 1989 by the US Department of Energy (DOE) and other agencies. Project goals for FY 1990 are also presented. An annual report of this type was a statutory requirement through January 1, 1986, pursuant to the Uranium Mill Tailings Radiation Control Act (UMTRCA) of 1978, Public Law (PL) 95--604. The DOE will continue to submit an annual report through project completion in order to inform the public of yearly project status. Title I of the UMTRCA authorizes the DOE, in cooperation with affected states and Indian tribes within whose boundaries designated uranium processing sites are located, to provide a program of assessment and remedial action at such sites. The purpose of the remedial action is to stabilize and control the tailings and other residual radioactive materials located on the inactive uranium processing sites in a safe and environmentally sound manner and to minimize or eliminate potential radiation health hazards. Commercial and residential properties in the vicinity of designated processing sites that are contaminated with material from the sites, herein referred to as vicinity properties,'' are also eligible for remedial action. Included in the UMTRA Project are 24 inactive uranium processing sites and associated vicinity properties located in 10 states, and the vicinity properties associated with Edgemont, South Dakota, an inactive uranium mill currently owned by the Tennessee Valley Authority (TVA).

Not Available

1989-12-01T23:59:59.000Z

179

Dismantlement and Radioactive Waste Management of DPRK Nuclear Facilities  

SciTech Connect (OSTI)

One critical aspect of any denuclearization of the Democratic Peoples Republic of Korea (DPRK) involves dismantlement of its nuclear facilities and management of their associated radioactive wastes. The decommissioning problem for its two principal operational plutonium facilities at Yongbyun, the 5MWe nuclear reactor and the Radiochemical Laboratory reprocessing facility, alone present a formidable challenge. Dismantling those facilities will create radioactive waste in addition to existing inventories of spent fuel and reprocessing wastes. Negotiations with the DPRK, such as the Six Party Talks, need to appreciate the enormous scale of the radioactive waste management problem resulting from dismantlement. The two operating plutonium facilities, along with their legacy wastes, will result in anywhere from 50 to 100 metric tons of uranium spent fuel, as much as 500,000 liters of liquid high-level waste, as well as miscellaneous high-level waste sources from the Radiochemical Laboratory. A substantial quantity of intermediate-level waste will result from disposing 600 metric tons of graphite from the reactor, an undetermined quantity of chemical decladding liquid waste from reprocessing, and hundreds of tons of contaminated concrete and metal from facility dismantlement. Various facilities for dismantlement, decontamination, waste treatment and packaging, and storage will be needed. The shipment of spent fuel and liquid high level waste out of the DPRK is also likely to be required. Nuclear facility dismantlement and radioactive waste management in the DPRK are all the more difficult because of nuclear nonproliferation constraints, including the call by the United States for complete, verifiable and irreversible dismantlement, or CVID. It is desirable to accomplish dismantlement quickly, but many aspects of the radioactive waste management cannot be achieved without careful assessment, planning and preparation, sustained commitment, and long completion times. The radioactive waste management problem in fact offers a prospect for international participation to engage the DPRK constructively. DPRK nuclear dismantlement, when accompanied with a concerted effort for effective radioactive waste management, can be a mutually beneficial goal.

Jooho, W.; Baldwin, G. T.

2005-04-01T23:59:59.000Z

180

Safe Operating Procedure SAFETY PROTOCOL: URANIUM  

E-Print Network [OSTI]

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

Farritor, Shane

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


181

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

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

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

182

Radioactive mixed waste disposal  

SciTech Connect (OSTI)

Various types of waste have been generated during the 50-year history of the Hanford Site. Regulatory changes in the last 20 years have provided the emphasis for better management of these wastes. Interpretations of the Atomic Energy Act of 1954 (AEA), the Resource Conservation and Recovery Act of 1976 (RCRA), and the Hazardous and Solid Waste Amendments (HSWA) have led to the definition of radioactive mixed wastes (RMW). The radioactive and hazardous properties of these wastes have resulted in the initiation of special projects for the management of these wastes. Other solid wastes at the Hanford Site include low-level wastes, transuranic (TRU), and nonradioactive hazardous wastes. This paper describes a system for the treatment, storage, and disposal (TSD) of solid radioactive waste.

Jasen, W.G.; Erpenbeck, E.G.

1993-02-01T23:59:59.000Z

183

Radioactive Waste Management Manual  

Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

This Manual further describes the requirements and establishes specific responsibilities for implementing DOE O 435.1, Radioactive Waste Management, for the management of DOE high-level waste, transuranic waste, low-level waste, and the radioactive component of mixed waste. Change 1 dated 6/19/01 removes the requirement that Headquarters is to be notified and the Office of Environment, Safety and Health consulted for exemptions for use of non-DOE treatment facilities. Certified 1-9-07. Admin Chg 2, dated 6-8-11, cancels DOE M 435.1-1 Chg 1.

1999-07-09T23:59:59.000Z

184

Container for radioactive materials  

DOE Patents [OSTI]

A container is claimed for housing a plurality of canister assemblies containing radioactive material. The several canister assemblies are stacked in a longitudinally spaced relation within a carrier to form a payload concentrically mounted within the container. The payload package includes a spacer for each canister assembly, said spacer comprising a base member longitudinally spacing adjacent canister assemblies from each other and sleeve surrounding the associated canister assembly for centering the same and conducting heat from the radioactive material in a desired flow path. 7 figures.

Fields, S.R.

1984-05-30T23:59:59.000Z

185

Uranium mining and milling sites remediation by COGEMA impact on the environment  

SciTech Connect (OSTI)

Mining and milling of any metal have a common impact on the environment. Because of radioactivity uranium ores and their residues generate specific potential hazards. First we quote the french regulation as regards to radioactive impact through the different pathways. Then we overview the different types of uranium mining wastes and the type of storage for milling residues; Objectives being set for the remediation we describe basic principles of the methodology and give a few examples from France and the US Monitoring goes on all through the active period of the site and is fitted to it after its remediation. To date, according to the measurements done in the environment, the added radiological impact is equivalent to the natural background.

Daroussin, J.L.; Pfiffelmann, J.P. [COGEMA, Velizy (France)

1994-12-31T23:59:59.000Z

186

Deep liquid-chromatographic purification of uranium extract from technetium  

SciTech Connect (OSTI)

The recycling of uranium in the nuclear fuel cycle requires the removal of a number of radioactive and stable impurities like {sup 99}Tc from spent fuels. In order to improve the grade of uranium extract purification from technetium the method of liquid chromatography and the apparatus for its performance have been developed. Process of technetium extraction and concentrating in aqueous solution containing reducing agent has been studied on simulated solutions (U-Tc-HNO{sub 3}-30% TBP-isoparM). The dynamic tests of the method have been carried out on the laboratory unit. Solution of diformyl-hydrazine in nitric acid was used as a stationary phase. Silica gel with specific surface of 186 m{sup 2}/g was used as a carrier of the stationary phase. It is shown that the volume of purified extract increases as the solution temperature increases, concentration of reducing agent increases and extract flow rate decreases. It is established that the technetium content in uranium by this method could achieve a value below 0.3 ppm. Some variants of overload and composition of the stationary phase containing the extracted technetium have been offered and tested. It is defined that the method provides reduction of processing medium-active wastes by more than 10 times during finish refining process. (authors)

Volk, V.; Dvoeglazov, K; Podrezova, L.; Vidanov, V.; Pavlyukevich, E. [OAO State Research Center - VNIINM, Rogov str., bld. 5, Moscow (Russian Federation)

2013-07-01T23:59:59.000Z

187

Radionuclides in the terrestrial ecosystem near a Canadian uranium mill -- Part 2: Small mammal food chains and bioavailability  

SciTech Connect (OSTI)

Food chain transfer through the soil-vegetation-small mammal food chain was measured by concentration ratios (CRs) for uranium, {sup 226}Ra, {sup 210}Pb, and {sup 210}Po at three sites near the Key Lake uranium mill in northern Saskatchewan. Plant/soil CRs, animal carcass/GI tract CRs, and animal/soil CRs were depressed at sites impacted by mill and tailings dusts relative to a nearby control site. Thus, radionuclides associated with large particulates in tailings and/or ore dusts may be less bioavailable to terrestrial plants and animals than natural sources of radioactive dust. These results show that reliance on default food chain transfer parameters, obtained from uncontaminated terrestrial ecosystems, may overpredict impacts at uranium mine and mill sites. Given the omnivorous diet of small mammals and birds, animal/soil CRs are recommended as the most cost-effective and robust means of predicting animal concentrations from environmental monitoring data at uranium mill facilities.

Thomas, P.A.

2000-06-01T23:59:59.000Z

188

Oxidation Protection of Uranium Nitride Fuel using Liquid Phase Sintering  

SciTech Connect (OSTI)

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

Dr. Paul A. Lessing

2012-03-01T23:59:59.000Z

189

Laser induced phosphorescence uranium analysis  

DOE Patents [OSTI]

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

Bushaw, Bruce A. (Kennewick, WA)

1986-01-01T23:59:59.000Z

190

Laser induced phosphorescence uranium analysis  

DOE Patents [OSTI]

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

Bushaw, B.A.

1983-06-10T23:59:59.000Z

191

Radioactive Waste Management  

Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

The objective of this Order is to ensure that all Department of Energy (DOE) radioactive waste is managed in a manner that is protective of worker and public health and safety and the environment. Cancels DOE O 5820.2A

1999-07-09T23:59:59.000Z

192

Sealed Radioactive Source Accountability  

Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

To establish Department of Energy (DOE) interim policy and to provide guidance for sealed radioactive source accountability. The directive does not cancel any directives. Extended by DOE N 5400.10 to 12-24-93 & Extended by DOE N 5400.12 to 12-24-94.

1991-12-24T23:59:59.000Z

193

Radioactive Waste Management  

Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

The objective of this Order is to ensure that all Department of Energy (DOE) radioactive waste is managed in a manner that is protective of worker and public health and safety and the environment. Cancels DOE O 5820.2A. Chg 1 dated 8-28-01. Certified 1-9-07.

1999-07-09T23:59:59.000Z

194

Sealed Radioactive Source Accountability  

Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

This Notice extends DOE N 5400.9, Sealed Radioactive Source Accountability, of 12-24-91, until 12-24-95, unless sooner superseded or rescinded. The contents of DOE N 5400.9 will be updated and incorporated in the revised DOE O 5480.11, Radiation Protection for Occupational Workers.

1994-12-22T23:59:59.000Z

195

Representativeness of large sample INAA in the study of Brazilian uranium mine waste  

SciTech Connect (OSTI)

Osamu Utsumi was the first uranium mine to be explored in Brazil and has been active for approximately two decades. It is located on the Poqos de Caldas plateau in the state of Minas Gerais, which is an area of the world with one of the highest levels of natural radioactivity. Mining activities were terminated in April 1996, leaving some tons of uranium at depths at which exploration is not economically viable. The decision to prematurely terminate mining activities was taken in light of the planned commissioning within 2 yr of a new mine in the state of Bahia in the Jazida da Cachoeira region, where a high-grade uranium ore is found. This paper describes the use of INAA for the analysis of wastes produced from ores.

De Nadai Fernandes, E.A. [Centro de Energia Nuclear na Agricultura, Piracicaba (Brazil); Bode, P. [Interfaculty Reactor Institute, Delft (Netherlands)

1997-12-01T23:59:59.000Z

196

Scientific basis for risk assessment and management of uranium mill tailings  

SciTech Connect (OSTI)

A National Research Council study panel, convened by the Board on Radioactive Waste Management, has examined the scientific basis for risk assessment and management of uranium mill tailings and issued this final report containing a number of recommendations. Chapter 1 provides a brief introduction to the problem. Chapter 2 examines the processes of uranium extraction and the mechanisms by which radionuclides and toxic chemicals contained in the ore can enter the environment. Chapter 3 is devoted to a review of the evidence on health risks associated with radon and its decay products. Chapter 4 provides a consideration of conventional and possible new technical alternatives for tailings management. Chapter 5 explores a number of issues of comparative risk, provides a brief history of uranium mill tailings regulation, and concludes with a discussion of choices that must be made in mill tailing risk management. 211 refs., 30 figs., 27 tabs.

Not Available

1986-01-01T23:59:59.000Z

197

Radioactive Contamination of Danish Territory  

E-Print Network [OSTI]

Risø-R-462 Radioactive Contamination of Danish Territory after Core-melt Accidents at the Barsebäck;#12;RIS0-R-462 RADIOACTIVE CONTAMINATION OF DANISH TERRITORY AFTER CORE-MELT ACCIDENTS AT THE BARSEBACK. An assessment is made of the radioactive contamination of Danish territory in the event of a core-melt accident

198

Radioactive Contamination of Danish Territory  

E-Print Network [OSTI]

» & Risø-R-462 Radioactive Contamination of Danish Territory after Core-melt Accidents 1982 Risø National Laboratory, DK-4000 Roskilde, Denmark #12;RIS?-R-462 RADIOACTIVE CONTAMINATION. Heikel Vinther, L. Warming and A. Aarkrog Abstract. An assessment is made of the radioactive

199

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

E-Print Network [OSTI]

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

American Society for Testing and Materials. Philadelphia

2007-01-01T23:59:59.000Z

200

Thermo-chemical Modelling of Uranium-free Nitride Fuels Mikael JOLKKONEN1;;y  

E-Print Network [OSTI]

and accepted December 22, 2003) A production process for americium-bearing, uranium-free nitride fuels environments was also estimated. We show that sintering of nitride compounds containing americium should be performed under nitrogen atmosphere in order to the avoid the excessive losses of americium reported from

Haviland, David

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


201

Systematic evaluation of satellite remote sensing for identifying uranium mines and mills.  

SciTech Connect (OSTI)

In this report, we systematically evaluate the ability of current-generation, satellite-based spectroscopic sensors to distinguish uranium mines and mills from other mineral mining and milling operations. We perform this systematic evaluation by (1) outlining the remote, spectroscopic signal generation process, (2) documenting the capabilities of current commercial satellite systems, (3) systematically comparing the uranium mining and milling process to other mineral mining and milling operations, and (4) identifying the most promising observables associated with uranium mining and milling that can be identified using satellite remote sensing. The Ranger uranium mine and mill in Australia serves as a case study where we apply and test the techniques developed in this systematic analysis. Based on literature research of mineral mining and milling practices, we develop a decision tree which utilizes the information contained in one or more observables to determine whether uranium is possibly being mined and/or milled at a given site. Promising observables associated with uranium mining and milling at the Ranger site included in the decision tree are uranium ore, sulfur, the uranium pregnant leach liquor, ammonia, and uranyl compounds and sulfate ion disposed of in the tailings pond. Based on the size, concentration, and spectral characteristics of these promising observables, we then determine whether these observables can be identified using current commercial satellite systems, namely Hyperion, ASTER, and Quickbird. We conclude that the only promising observables at Ranger that can be uniquely identified using a current commercial satellite system (notably Hyperion) are magnesium chlorite in the open pit mine and the sulfur stockpile. Based on the identified magnesium chlorite and sulfur observables, the decision tree narrows the possible mineral candidates at Ranger to uranium, copper, zinc, manganese, vanadium, the rare earths, and phosphorus, all of which are milled using sulfuric acid leaching.

Blair, Dianna Sue; Stork, Christopher Lyle; Smartt, Heidi Anne; Smith, Jody Lynn

2006-01-01T23:59:59.000Z

202

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

E-Print Network [OSTI]

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

Helmreich, Grant

2012-02-14T23:59:59.000Z

203

The Hazard Posed by Depleted Uranium Munitions  

E-Print Network [OSTI]

This paper assesses the radiological and chemical hazards resulting from the use of depleted uranium (DU) munitions. Due to the low radioactivity of DU, radiological hazards to individuals would become significant in comparison to natural background radiation doses only in cases of prolonged contact---for example, when shards of a DU penetrator remain embedded in a soldier's body. Although the radiation doses to virtually all civilians would be very low, the cumulative "population dose" resulting from the dispersal of hundreds of tons of DU, as occurred during the Gulf War, could result in up to ten cancer deaths. It is highly unlikely that exposures of persons downwind from the use of DU munitions or consuming food or water contaminated by DU dust would reach the estimated threshold for chemical heavy-metal effects. The exposures of soldiers in vehicles struck by DU munitions could be much higher, however, and persons who subsequently enter such vehicles without adequate respiratory protection could potentially be at risk. Soldiers should be trained to avoid unnecessary exposure to DU, and vehicles struck by DU munitions should be made inaccessible to curious civilians. INTRODUCTION

Steve Fetter And; Steve Fetter A

204

Introduction to naturally occurring radioactive material  

SciTech Connect (OSTI)

Naturally occurring radioactive material (NORM) is everywhere; we are exposed to it every day. It is found in our bodies, the food we eat, the places where we live and work, and in products we use. We are also bathed in a sea of natural radiation coming from the sun and deep space. Living systems have adapted to these levels of radiation and radioactivity. But some industrial practices involving natural resources concentrate these radionuclides to a degree that they may pose risk to humans and the environment if they are not controlled. Other activities, such as flying at high altitudes, expose us to elevated levels of NORM. This session will concentrate on diffuse sources of technologically-enhanced (TE) NORM, which are generally large-volume, low-activity waste streams produced by industries such as mineral mining, ore benefication, production of phosphate Fertilizers, water treatment and purification, and oil and gas production. The majority of radionuclides in TENORM are found in the uranium and thorium decay chains. Radium and its subsequent decay products (radon) are the principal radionuclides used in characterizing the redistribution of TENORM in the environment by human activity. We will briefly review other radionuclides occurring in nature (potassium and rubidium) that contribute primarily to background doses. TENORM is found in many waste streams; for example, scrap metal, sludges, slags, fluids, and is being discovered in industries traditionally not thought of as affected by radionuclide contamination. Not only the forms and volumes, but the levels of radioactivity in TENORM vary. Current discussions about the validity of the linear no dose threshold theory are central to the TENORM issue. TENORM is not regulated by the Atomic Energy Act or other Federal regulations. Control and regulation of TENORM is not consistent from industry to industry nor from state to state. Proposed regulations are moving from concentration-based standards to dose-based standards. So when is TENORM a problem? Where is it a problem? That depends on when, where, and whom you talk to! We will start by reviewing background radioactivity, then we will proceed to the geology, mobility, and variability of these radionuclides. We will then review some of the industrial sectors affected by TENORM, followed by a brief discussion on regulatory aspects of the issue.

Egidi, P.

1997-08-01T23:59:59.000Z

205

Radioactive ion detector  

DOE Patents [OSTI]

Apparatus for detecting the presence, in aqueous media, of substances which emit alpha and/or beta radiation and determining the oxidation state of these radioactive substances, that is, whether they are in cationic or anionic form. In one embodiment, a sensor assembly has two elements, one comprised of an ion-exchange material which binds cations and the other comprised of an ion-exchange material which binds anions. Each ion-exchange element is further comprised of a scintillation plastic and a photocurrent generator. When a radioactive substance to which the sensor is exposed binds to either element and emits alpha or beta particles, photons produced in the scintillation plastic illuminate the photocurrent generator of that element. Sensing apparatus senses generator output and thereby indicates whether cationic species or anionic species or both are present and also provides an indication of species quantity. 2 figs.

Bower, K.E.; Weeks, D.R.

1997-08-12T23:59:59.000Z

206

Radioactive ion detector  

DOE Patents [OSTI]

Apparatus for detecting the presence, in aqueous media, of substances which emit alpha and/or beta radiation and determining the oxidation state of these radioactive substances, that is, whether they are in cationic or anionic form. In one embodiment, a sensor assembly has two elements, one comprised of an ion-exchange material which binds cations and the other comprised of an ion-exchange material which binds anions. Each ion-exchange element is further comprised of a scintillation plastic and a photocurrent generator. When a radioactive substance to which the sensor is exposed binds to either element and emits alpha or beta particles, photons produced in the scintillation plastic illuminate the photocurrent generator of that element. Sensing apparatus senses generator output and thereby indicates whether cationic species or anionic species or both are present and also provides an indication of species quantity.

Bower, Kenneth E. (Los Alamos, NM); Weeks, Donald R. (Saratoga, CA)

1997-01-01T23:59:59.000Z

207

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

E-Print Network [OSTI]

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

Fayek, Mostafa

208

Precipitate hydrolysis process for the removal of organic compounds from nuclear waste slurries  

DOE Patents [OSTI]

A process for removing organic compounds from a nuclear waste slurry comprising reacting a mixture of radioactive waste precipitate slurry and an acid in the presence of a catalytically effective amount of a copper(II) catalyst whereby the organic compounds in the precipitate slurry are hydrolyzed to form volatile organic compounds which are separated from the reacting mixture. The resulting waste slurry, containing less than 10 percent of the original organic compounds, is subsequently blended with high level radioactive sludge land transferred to a vitrification facility for processing into borosilicate glass for long-term storage. 2 figs., 3 tabs.

Doherty, J.P.; Marek, J.C.

1987-02-25T23:59:59.000Z

209

Precipitate hydrolysis process for the removal of organic compounds from nuclear waste slurries  

DOE Patents [OSTI]

A process for removing organic compounds from a nuclear waste slurry comprising reacting a mixture of radioactive waste precipitate slurry and an acid in the presence of a catalytically effective amount of a copper (II) catalyst whereby the organic compounds in the precipitate slurry are hydrolyzed to form volatile organic compounds which are separated from the reacting mixture. The resulting waste slurry, containing less than 10 percent of the orginal organic compounds, is subsequently blended with high level radioactive sludge and transferred to a virtrification facility for processing into borosilicate glass for long-term storage.

Doherty, Joseph P. (Elkton, MD); Marek, James C. (Augusta, GA)

1989-01-01T23:59:59.000Z

210

Inherently safe in situ uranium recovery  

DOE Patents [OSTI]

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

Krumhansl, James L; Brady, Patrick V

2014-04-29T23:59:59.000Z

211

Uranium Acquisition | Y-12 National Security Complex  

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

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

212

The End of Cheap Uranium  

E-Print Network [OSTI]

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

Dittmar, Michael

2011-01-01T23:59:59.000Z

213

Environmental assessment of remedial action at the Naturita uranium processing site near Naturita, Colorado: Revision 5  

SciTech Connect (OSTI)

Title 1 of the Uranium Mill Tailings Radiation Control Act (UMTRCA) of 1978, Public Law (PL) 95-604, authorized the US Department of Energy (DOE) to perform remedial action at the inactive Naturita, Colorado, uranium processing site to reduce the potential health effects from the radioactive materials at the site and at vicinity properties associated with the site. Title 2 of the UMTRCA authorized the US Nuclear Regulatory Commission (NRC) or agreement state to regulate the operation and eventual reclamation of active uranium processing sites. The uranium mill tailings at the site were removed and reprocessed from 1977 to 1979. The contaminated areas include the former tailings area, the mill yard, the former ore storage area, and adjacent areas that were contaminated by uranium processing activities and wind and water erosion. The Naturita remedial action would result in the loss of 133 acres (ac) of contaminated soils at the processing site. If supplemental standards are approved by the NRC and the state of Colorado, approximately 112 ac of steeply sloped contaminated soils adjacent to the processing site would not be cleaned up. Cleanup of this contamination would have adverse environmental consequences and would be potentially hazardous to remedial action workers.

Not Available

1994-10-01T23:59:59.000Z

214

Baseline risk assessment of groundwater contamination at the Uranium Mill Tailings Site near Gunnison, Colorado  

SciTech Connect (OSTI)

This Baseline Risk Assessment of Groundwater Contamination at the Uranium Mill Tailings Site Near Gunnison, Colorado evaluates potential impacts to public health or the environment resulting from groundwater contamination at the former uranium mill processing site. The tailings and other contaminated material at this site are being placed in an off-site disposal cell by the US Department of Energy`s (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project. Currently, the UMTRA Project is evaluating groundwater contamination. This is the second risk assessment of groundwater contamination at this site. The first risk assessment was performed primarily to evaluate existing domestic wells. This risk assessment evaluates the most contaminated monitor wells at the processing site. It will be used to assist in determining what remedial action is needed for contaminated groundwater at the site after the tailings are relocated. This risk assessment follows an approach outlined by the US Environmental Protection Agency (EPA). The first step is to evaluate groundwater data collected from monitor wells at the site. Evaluation of these data showed that the main contaminants in the groundwater are cadmium, cobalt, iron, manganese, sulfate, uranium, and some of the products of radioactive decay of uranium.

Not Available

1993-12-01T23:59:59.000Z

215

Surface Decontamination of System Components in Uranium Conversion Plant at KAERI  

SciTech Connect (OSTI)

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

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

2003-02-25T23:59:59.000Z

216

Lawrence Berkeley National Laboratory 1996 Site Environmental Report Vol. I  

E-Print Network [OSTI]

radioactive. uranium, depleted Uranium consisting primarilyoccurring in nature, depleted uranium is man-made. uranium,

2010-01-01T23:59:59.000Z

217

Thorium and uranium diphosphonates: Syntheses, structures, and spectroscopic properties  

SciTech Connect (OSTI)

Four new thorium and uranium diphosphonate compounds, [H{sub 3}O]{l_brace}Th{sub 2}[C{sub 6}H{sub 4}(PO{sub 3}){sub 2}]{sub 2}F{r_brace} (Thbbp-1), An{sub 2}{l_brace}(O{sub 3}PC{sub 6}H{sub 4}PO{sub 3}H){sub 2}[C{sub 6}H{sub 4}(PO{sub 3}H){sub 2}]{r_brace} [An=Th(IV), U(IV)] (Thbbp-2)/(U4bbp), and [(C{sub 2}H{sub 5})(CH{sub 3}){sub 3}N][(UO{sub 2}){sub 3}(O{sub 3}PC{sub 6}H{sub 4}PO{sub 3}H){sub 2}F(H{sub 2}O)] (U6bbp) have been synthesized hydrothermally using 1,4-benzenebisphosphonic acid as ligand. The crystal structures of these compounds were determined by single crystal X-ray diffraction. Thbbp-1 and Thbbp-2 contain seven-coordinate Th(IV) within ThO{sub 6}F and ThO{sub 7} units with capped trigonal prismatic and capped octahedral geometries, respectively. U4bbp is isotypic with Thbbp-2. The structure of U6bbp contains U(VI) is the common seven-coordinate pentagonal bipyramid. - Graphical abstract: Coordination polyhedra and luminescence properties in thorium and uranium compounds. Highlights: Black-Right-Pointing-Pointer Three-dimensional thorium and uranium complexes. Black-Right-Pointing-Pointer Conversion of U(VI) to U(IV) under hydrothermal condition. Black-Right-Pointing-Pointer Unusual seven-coordinate thorium complexes exhibiting capped octahedral and capped trigonal prismatic geometries.

Adelani, Pius O. [Department of Civil Engineering and Geological Sciences, and Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556 (United States); Albrecht-Schmitt, Thomas E., E-mail: talbrec1@nd.edu [156 Fitzpatrick Hall, University of Notre Dame, Notre Dame, IN 46556 (United States)

2012-08-15T23:59:59.000Z

218

High strength uranium-tungsten alloys  

DOE Patents [OSTI]

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

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

1991-01-01T23:59:59.000Z

219

High strength uranium-tungsten alloy process  

DOE Patents [OSTI]

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

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

1990-01-01T23:59:59.000Z

220

Clean Air Act Requirements: Uranium Mill Tailings  

E-Print Network [OSTI]

EPA'S Clean Air Act Requirements: Uranium Mill Tailings Radon Emissions Rulemaking Reid J. Rosnick requirements for operating uranium mill tailings (Subpart W) Status update on Subpart W activities Outreach/Communications #12;3 EPA Regulatory Requirements for Operating Uranium Mill Tailings (Clean Air Act) · 40 CFR 61

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


221

URANIUM MILL TAILINGS RADON FLUX CALCULATIONS  

E-Print Network [OSTI]

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

222

Remediation and Recovery of Uranium from Contaminated  

E-Print Network [OSTI]

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

Lovley, Derek

223

Uranium Watch REGULATORY CONFUSION: FEDERALAND STATE  

E-Print Network [OSTI]

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

224

D Riso-R-429 Automated Uranium  

E-Print Network [OSTI]

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

225

Y-12 Uranium Exposure Study  

SciTech Connect (OSTI)

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

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

1999-08-05T23:59:59.000Z

226

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

SciTech Connect (OSTI)

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

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

2012-07-25T23:59:59.000Z

227

Radioactive waste material disposal  

DOE Patents [OSTI]

The invention is a process for direct conversion of solid radioactive waste, particularly spent nuclear fuel and its cladding, if any, into a solidified waste glass. A sacrificial metal oxide, dissolved in a glass bath, is used to oxidize elemental metal and any carbon values present in the waste as they are fed to the bath. Two different modes of operation are possible, depending on the sacrificial metal oxide employed. In the first mode, a regenerable sacrificial oxide, e.g., PbO, is employed, while the second mode features use of disposable oxides such as ferric oxide. 3 figs.

Forsberg, C.W.; Beahm, E.C.; Parker, G.W.

1995-10-24T23:59:59.000Z

228

Radioactive waste material disposal  

DOE Patents [OSTI]

The invention is a process for direct conversion of solid radioactive waste, particularly spent nuclear fuel and its cladding, if any, into a solidified waste glass. A sacrificial metal oxide, dissolved in a glass bath, is used to oxidize elemental metal and any carbon values present in the waste as they are fed to the bath. Two different modes of operation are possible, depending on the sacrificial metal oxide employed. In the first mode, a regenerable sacrificial oxide, e.g., PbO, is employed, while the second mode features use of disposable oxides such as ferric oxide.

Forsberg, Charles W. (155 Newport Dr., Oak Ridge, TN 37830); Beahm, Edward C. (106 Cooper Cir., Oak Ridge, TN 37830); Parker, George W. (321 Dominion Cir., Knoxville, TN 37922)

1995-01-01T23:59:59.000Z

229

Geo-neutrinos and the Radioactive Power of the Earth  

E-Print Network [OSTI]

Chemical and physical Earth models agree little as to the radioactive power of the planet. Each predicts a range of radioactive powers, overlapping slightly with the other at about 24 TW, and together spanning 14-46 TW. Approximately 20 % of this radioactive power (3-8 TW) escapes to space in the form of geo-neutrinos. The remaining 11-38 TW heats the planet with significant geo-dynamical consequences, appearing as the radiogenic component of the 43-49 TW surface heat flow. The non-radiogenic component of the surface heat flow (5-38 TW) is presumably primordial, a legacy of the formation and early evolution of the planet. A constraining measurement of radiogenic heating provides insights to the thermal history of the Earth and potentially discriminates chemical and physical Earth models. Radiogenic heating in the planet primarily springs from unstable nuclides of uranium, thorium, and potassium. The paths to their stable daughter nuclides include nuclear beta decays, producing geo-neutrinos. Large sub-surface detectors efficiently record the energy but not the direction of the infrequent interactions of the highest energy geo-neutrinos, originating only from uranium and thorium. The measured energy spectrum of the interactions estimates the relative amounts of these heat-producing elements, while the intensity estimates planetary radiogenic power. Recent geo-neutrino observations in Japan and Italy find consistent values of radiogenic heating. The combined result mildly excludes the lowest model values of radiogenic heating and, assuming whole mantle convection, identifies primordial heat loss. Future observations have the potential to measure radiogenic heating with better precision, further constraining geological models and the thermal evolution of the Earth.

Steve Dye

2012-09-11T23:59:59.000Z

230

Process for alloying uranium and niobium  

DOE Patents [OSTI]

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

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

1991-01-01T23:59:59.000Z

231

Remedial Action Plan and site design for stabilization of the inactive uranium mill tailings site at Falls City, Texas. [Uranium Mill Tailings Remedial Action (UMTRA) Project  

SciTech Connect (OSTI)

The uranium processing site near Falls City, Texas, was one of 24 inactive uranium mill sites designated to be remediated by the US Department of Energy (DOE) under Title I of the Uranium Mill Tailings Radiation Control Act of 1978 (UMTRCA). The UMTRCA requires that the US Nuclear Regulatory Commission (NRC) concur with the DOE's remedial action plan (RAP) and certify that the remedial action conducted at the site complies with the standards promulgated by the US Environmental Protection Agency (EPA). The RAP, which includes this summary remedial action selection report (RAS), serves a two-fold purpose. First, it describes the activities proposed by the DOE to accomplish long-term stabilization and control of the residual radioactive materials at the inactive uranium processing site near Falls City, Texas. Second, this document and the remainder of the RAP, upon concurrence and execution by the DOE, the State of Texas, and the NRC, becomes Appendix B of the Cooperative Agreement between the DOE and the State of Texas.

Chernoff, A.R. (USDOE Albuquerque Field Office, NM (United States). Uranium Mill Tailings Remedial Action Project Office); Lacker, D.K. (Texas State Dept. of Health, Austin, TX (United States). Bureau of Radiation Control)

1992-09-01T23:59:59.000Z

232

Uranium Recovery Surface Activities (Texas)  

Broader source: Energy.gov [DOE]

This section of the Texas Commission on Environmental Quality enforces and makes the rules and regulations for handling and recovering radioactive materials associated with in situ mining in Texas....

233

Uranium 2014 resources, production and demand  

E-Print Network [OSTI]

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

Organisation for Economic Cooperation and Development. Paris

2014-01-01T23:59:59.000Z

234

Uranium 2005 resources, production and demand  

E-Print Network [OSTI]

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

Organisation for Economic Cooperation and Development. Paris

2006-01-01T23:59:59.000Z

235

Radioactive waste processing apparatus  

DOE Patents [OSTI]

Apparatus for use in processing radioactive waste materials for shipment and storage in solid form in a container is disclosed. The container includes a top, and an opening in the top which is smaller than the outer circumference of the container. The apparatus includes an enclosure into which the container is placed, solution feed apparatus for adding a solution containing radioactive waste materials into the container through the container opening, and at least one rotatable blade for blending the solution with a fixing agent such as cement or the like as the solution is added into the container. The blade is constructed so that it can pass through the opening in the top of the container. The rotational axis of the blade is displaced from the center of the blade so that after the blade passes through the opening, the blade and container can be adjusted so that one edge of the blade is adjacent the cylindrical wall of the container, to insure thorough mixing. When the blade is inside the container, a substantially sealed chamber is formed to contain vapors created by the chemical action of the waste solution and fixant, and vapors emanating through the opening in the container.

Nelson, Robert E. (Lombard, IL); Ziegler, Anton A. (Darien, IL); Serino, David F. (Maplewood, MN); Basnar, Paul J. (Western Springs, IL)

1987-01-01T23:59:59.000Z

236

Radiation Awareness TrainingRadiation Awareness Training Radioactive Material &Radioactive Material &  

E-Print Network [OSTI]

quarterly · Radioactive waste retrieval, storage, disposal · Dosimetry exchange · Leak tests of sealedRadiation Awareness TrainingRadiation Awareness Training Radioactive Material &Radioactive Material, Chemistry, Physics, Applied Physiology · Radioactive Material ­ Sealed Sources, Unsealed Sources (liquid

Sherrill, David

237

RSSC RADIOACTIVE WASTE DISPOSAL 08/2011 7-1 RADIOACTIVE WASTE DISPOSAL  

E-Print Network [OSTI]

RSSC RADIOACTIVE WASTE DISPOSAL 08/2011 7-1 CHAPTER 7 RADIOACTIVE WASTE DISPOSAL PAGE I. Radioactive Waste Disposal ............................................................................................ 7-2 II. Radiation Control Technique #2 Instructions for Preparation of Radioactive Waste

Slatton, Clint

238

Method for acid oxidation of radioactive, hazardous, and mixed organic waste materials  

DOE Patents [OSTI]

The present invention is directed to a process for reducing the volume of low level radioactive and mixed waste to enable the waste to be more economically stored in a suitable repository, and for placing the waste into a form suitable for permanent disposal. The invention involves a process for preparing radioactive, hazardous, or mixed waste for storage by contacting the waste starting material containing at least one organic carbon-containing compound and at least one radioactive or hazardous waste component with nitric acid and phosphoric acid simultaneously at a contacting temperature in the range of about 140.degree. C. to about 210 .degree. C. for a period of time sufficient to oxidize at least a portion of the organic carbon-containing compound to gaseous products, thereby producing a residual concentrated waste product containing substantially all of said radioactive or inorganic hazardous waste component; and immobilizing the residual concentrated waste product in a solid phosphate-based ceramic or glass form.

Pierce, Robert A. (Aiken, SC); Smith, James R. (Corrales, NM); Ramsey, William G. (Aiken, SC); Cicero-Herman, Connie A. (Aiken, SC); Bickford, Dennis F. (Folly Beach, SC)

1999-01-01T23:59:59.000Z

239

Exotic fission properties of highly neutron-rich Uranium isotopes  

E-Print Network [OSTI]

The series of Uranium isotopes with $N=154 \\sim 172$ around the magic number N=162/164 are identified to be thermally fissile. The thermal neutron fission of a typical representative $^{249}$U of this region amenable to synthesis in the radioactive ion beam facilities is considered here. Semiempirical study of fission barrier height and width shows this nucleus to be infinitely stable against spontaneous fission due to increase in barrier width arising out of excess neutrons. Calculation of probability of fragment mass yields and microscopic study in relativistic mean field theory, show this nucleus to undergo a new mode of thermal fission decay termed {\\it multifragmentation fission} where a number of prompt scission neutrons are simultaneously released along with the two heavy fission fragments.

L. Satpathy; S. K. Patra; R. K. Choudhury

2007-03-05T23:59:59.000Z

240

CHERNOBYL DATA BASE ENVIRONMENTAL RADIOACTIVITY  

E-Print Network [OSTI]

MAY 1990 THE NORDIC CHERNOBYL DATA BASE ENVIRONMENTAL RADIOACTIVITY MEASUREMENTS Nordic liaison CHERNOBYL DATA BASE ENVIRONMENTAL RADIOACTIVITY MEASUREMENTS Final Report of the NKA Project AKT 242 Edited the members of the working group. Graphic Systems AB, Malmo 1990 #12;111 ABSTRACT. The NORDIC CHERNOBYL DATA

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


241

Radioactive Material Transportation Practices Manual  

Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

This Manual establishes standard transportation practices for the Department of Energy, including National Nuclear Security Administration to use in planning and executing offsite shipments of radioactive materials and waste. The revision reflects ongoing collaboration of DOE and outside organizations on the transportation of radioactive material and waste. Cancels DOE M 460.2-1.

2008-06-04T23:59:59.000Z

242

The potential human health effect(s) of the metal uranium in the environment. Report on the known human health effects associated with the exposure to the metal uranium  

SciTech Connect (OSTI)

Concern over the levels of the metal uranium in the environment as a result of industrial activities has been expressed by several Federal and State agencies. This concern is associated with potential human health effects of this metal on kidney function and bone formation. Although limits for the Metal uranium in the environment remain to be set, the Environmental Protection Agency (EPA) is currently in the process of establishing guidance limits for this metal in water and soil. These limits will be established for both the metal and the associated radioactivity. The suggested limits currently being considered for water and soil are, 20 pCi/liter and 10 pCi/gram wet weight, respectively. For naturally occurring uranium EPA assumes that 1 ug of uranium metal equals 0.67 pCi at equilibrium (i.e. at equilibrium the mass ratio of {sup 234}uranium to {sup 238}uranium is small but their activities are equal). Thus the limits for water and soil on weight basis for the uranium metal would be 30 ug/liter and 15 ug/gram wet weight, respectively. These limits are being established based on the potential increase in cancer death in populations that exceed this limit. Since there does not appear to be a significant correlation between cancer deaths and.uranium metal exposure (see discussion below), these limits will probably be established based on the known association between radionuclides exposure and cancer deaths. The exposure limits for other health effects such as kidney damage and retardation in bone formation apparently are not being considered by EPA.

Not Available

1990-12-31T23:59:59.000Z

243

Radioactivity in Food and the Environment, 2009  

E-Print Network [OSTI]

................................................................................................................22 1.2.1 Radioactive waste disposal from nuclear sites ............................................................................................................................22 1.2 Disposals of radioactive waste ..............................................................................................................27 1.2.5 Solid radioactive waste disposal at sea

244

Radioactivity in Food and the Environment, 2006  

E-Print Network [OSTI]

................................................................................................................22 1.2.1 Radioactive waste disposal from nuclear sites .............................................................................................................................22 1.2 Disposals of radioactive waste.......................................................................................................25 1.2.5 Solid radioactive waste disposal at sea

245

Environmental assessment of remedial action at the Slick Rock uranium mill tailings sites, Slick Rock, Colorado  

SciTech Connect (OSTI)

The Uranium Mill Tailings Radiation Control Act of 1978, hereafter referred to as the UMTRCA, authorized the US Department of Energy (DOE) to clean up two uranium mill tailings processing sites near Slick Rock, Colorado, in San Miguel County. The purpose of the cleanup is to reduce the potential health effects associated with the radioactive materials remaining on the processing sites and on vicinity properties (VPs) associated with the sites. The US Environmental Protection Agency (EPA) promulgated standards for the UMTRCA that contained measures to control the contaminated materials and to protect the ground water from further degradation. The sites contain concrete foundations of mill buildings, tailings piles, and areas contaminated by windblown and waterborne radioactive tailings materials. The proposed action is to remediate the UC and NC sites by removing all contaminated materials within the designated site boundaries or otherwise associated with the sites, and relocating them to, and stabilizing them at, a location approximately 5 road mi (8 km) northeast of the processing sites on land administered by the US Bureau of Land Management (BLM). Remediation would be performed by the DOE`s Uranium Mill Tailings Remedial Action (UMTRA) Project.

NONE

1995-01-01T23:59:59.000Z

246

Uranium mine and mill tailings - Liabilities in the European Union  

SciTech Connect (OSTI)

Available in abstract form only. Full text of publication follows: Uranium mining and milling has taken place on large scale in the Member States of the European Union (EU) for some 60 years. Although, compared to mining, milling activities are normally concentrated in fewer locations, this can still result in a relatively large number of disposal sites for the tailings, compared to other radioactive wastes. In addition these sites are also quite large, in terms of both volume and surface area. Coupled with the residual uranium in the tailings together with other radionuclides, heavy metals, chemicals etc this results in an environmental legacy continuing far into the future. Often during production no or little provision has been made for the closure, remediation and future supervision of such sites. In 1996 the European Commission funded an inventory of uranium mining and milling liabilities in nine Central and Eastern European Countries. Additionally, pilot projects were funded to carry out remediation activities at several sites. Almost ten years later the Commission has identified the need to address the situation of these large liabilities in all EU Member States and to assess the progress made in remediation of the sites, especially in view of the closure of almost all mining activities in Europe. The Commission study has identified the current tailings liabilities in Europe, their status, the future plans for these sites and the hazards that continue to be associated with them. It is clear that although considerable progress has been made in recent years, much work remains to be carried out in the areas of remediation, and ensuring the long-term safety of many of the identified objects. The paper presents the main findings of the study, as well as the challenges identified to ensure long-term safety of these wastes. (authors)

Hilden, Wolfgang; Murphy, Simon [European Commission, Maison de l'Europe, L-2920 (Luxembourg); Vrijen, Jan [KARUWEEG BV, Leliendaalsedreef 9, 4333 JZ Middelburg (Netherlands)

2007-07-01T23:59:59.000Z

247

UMTRA (Uranium Mill Tailings Remedial Action) Project site management manual  

SciTech Connect (OSTI)

The purpose of this manual is to summarize the organizational interfaces and the technical approach used to manage the planning, design development, National Environmental Policy Act (NEPA) compliance, engineering, and remedial action required to stabilize and control the designated Uranium Mill Tailings Remedial Action (UMTRA) Project sites. This manual describes the Project's objective, participants' roles and responsibilities, technical approach for accomplishing the objective, and planning and managerial controls to be used in performing the site work. The narrative follows the flow of activities depicted in Figure 1.1, which provides the typical sequence of key Project activities. A list of acronyms used is presented at the end of the manual. The comparable manual for UMTRA Project vicinity properties is the Vicinity Properties Management and Implementation Manual'' (VPMIM) (UMTRA-DOE/AL-050601). Together, the two manuals cover the remedial action activities associated with UMTRA Project sites. The UMTRA Project's objective is to stabilize and control the uranium mill tailings, vicinity property materials, and other residual radioactive materials at the designated sites (Figure 1.2) in a safe and environmentally sound manner in order to minimize radiation health hazards to the public. 26 figs., 6 tabs.

Not Available

1990-10-01T23:59:59.000Z

248

Uranium Mill Tailings Remedial Action Project 1994 environmental report  

SciTech Connect (OSTI)

This annual report documents the Uranium Mill Tailings Remedial Action (UMTRA) Project environmental monitoring and protection program. The UMTRA Project routinely monitors radiation, radioactive residual materials, and hazardous constituents at associated former uranium tailings processing sites and disposal sites. At the end of 1994, surface remedial action was complete at 14 of the 24 designated UMTRA Project processing sites: Canonsburg, Pennsylvania; Durango, Colorado; Grand Junction, Colorado; Green River Utah, Lakeview, Oregon; Lowman, Idaho; Mexican Hat, Utah; Riverton, Wyoming; Salt Lake City, Utah; Falls City, Texas; Shiprock, New Mexico; Spook, Wyoming, Tuba City, Arizona; and Monument Valley, Arizona. Surface remedial action was ongoing at 5 sites: Ambrosia Lake, New Mexico; Naturita, Colorado; Gunnison, Colorado; and Rifle, Colorado (2 sites). Remedial action has not begun at the 5 remaining UMTRA Project sites that are in the planning stage. Belfield and Bowman, North Dakota; Maybell, Colorado; and Slick Rock, Colorado (2 sites). The ground water compliance phase of the UMTRA Project started in 1991. Because the UMTRA Project sites are.` different stages of remedial action, the breadth of the UMTRA environmental protection program differs from site to site. In general, sites actively undergoing surface remedial action have the most comprehensive environmental programs for sampling media. At sites where surface remedial action is complete and at sites where remedial action has not yet begun, the environmental program consists primarily of surface water and ground water monitoring to support site characterization, baseline risk assessments, or disposal site performance assessments.

NONE

1995-08-01T23:59:59.000Z

249

Elements & Compounds Atoms (Elements)  

E-Print Network [OSTI]

#12;Elements & Compounds #12;Atoms (Elements) Molecules (Compounds) Cells Elements & Compounds #12 #12;First shell Second shell Third shell Hydrogen 1H Lithium 3Li Sodium 11Na Beryllium 4Be Magnesium energy Higher energy (a) A ball bouncing down a flight of stairs provides an analogy for energy levels

Frey, Terry

250

Remedial action plan for the inactive Uranium Processing Site at Naturita, Colorado. Remedial action plan: Attachment 2, Geology report, Attachment 3, Ground water hydrology report: Working draft  

SciTech Connect (OSTI)

The uranium processing site near Naturita, Colorado, is one of 24 inactive uranium mill sites designated to be cleaned up by the US Department of Energy (DOE) under the Uranium Mill Tailings Radiation Control Act of 1978 (UMTRCA), 42 USC {section}7901 et seq. Part of the UMTRCA requires that the US Nuclear Regulatory Commission (NRC) concur with the DOE`s remedial action plan (RAP) and certify that the remedial action conducted at the site complies with the standards promulgated by the US Environmental Protection Agency (EPA). This RAP serves two purposes. First, it describes the activities that are proposed by the DOE to accomplish remediation and long-term stabilization and control of the radioactive materials at the inactive uranium processing site near Naturita, Colorado. Second, this RAP, upon concurrence and execution by the DOE, the state of Colorado, and the NRC, become Appendix B of the cooperative agreement between the DOE and the state of Colorado.

Not Available

1994-09-01T23:59:59.000Z

251

Reports on investigations of uranium anomalies. National Uranium Resource Evaluation  

SciTech Connect (OSTI)

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

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

1982-10-01T23:59:59.000Z

252

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

E-Print Network [OSTI]

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

Matthews, Isaac A

2010-01-01T23:59:59.000Z

253

Uranium 2009 resources, production and demand  

E-Print Network [OSTI]

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

Organisation for Economic Cooperation and Development. Paris

2010-01-01T23:59:59.000Z

254

Uranium Metal Analysis via Selective Dissolution  

SciTech Connect (OSTI)

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

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

2008-09-10T23:59:59.000Z

255

Depleted uranium disposal options evaluation  

SciTech Connect (OSTI)

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

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

1994-05-01T23:59:59.000Z

256

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

E-Print Network [OSTI]

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

Boyer, Edmond

257

Method for the simultaneous recovery of radionuclides from liquid radioactive wastes using a solvent  

DOE Patents [OSTI]

The present invention relates to solvents, and methods, for selectively extracting and recovering radionuclides, especially cesium and strontium, rare earths and actinides from liquid radioactive wastes. More specifically, the invention relates to extracting agent solvent compositions comprising complex organoboron compounds, substituted polyethylene glycols, and neutral organophosphorus compounds in a diluent. The preferred solvent comprises a chlorinated cobalt dicarbollide, diphenyl-dibutylmethylenecarbamoylphosphine oxide, PEG-400, and a diluent of phenylpolyfluoroalkyl sulfone. The invention also provides a method of using the invention extracting agents to recover cesium, strontium, rare earths and actinides from liquid radioactive waste.

Romanovskiy, Valeriy Nicholiavich (St. Petersburg, RU); Smirnov, Igor V. (St. Petersburg, RU); Babain, Vasiliy A. (St. Petersburg, RU); Todd, Terry A. (Aberdeen, ID); Brewer, Ken N. (Arco, ID)

2001-01-01T23:59:59.000Z

258

Solvent for the simultaneous recovery of radionuclides from liquid radioactive wastes  

DOE Patents [OSTI]

The present invention relates to solvents, and methods, for selectively extracting and recovering radionuclides, especially cesium and strontium, rare earths and actinides from liquid radioactive wastes. More specifically, the invention relates to extracting agent solvent compositions comprising complex organoboron compounds, substituted polyethylene glycols, and neutral organophosphorus compounds in a diluent. The preferred solvent comprises a chlorinated cobalt dicarbollide, diphenyl-dibutylmethylenecarbamoylphosphine oxide, PEG-400, and a diluent of phenylpolyfluoroalkyl sulfone. The invention also provides a method of using the invention extracting agents to recover cesium, strontium, rare earths and actinides from liquid radioactive waste.

Romanovskiy, Valeriy Nicholiavich (St. Petersburg, RU); Smirnov, Igor V. (St. Petersburg, RU); Babain, Vasiliy A. (St. Petersburg, RU); Todd, Terry A. (Aberdeen, ID); Brewer, Ken N. (Arco, ID)

2002-01-01T23:59:59.000Z

259

Dry process fluorination of uranium dioxide using ammonium bifluoride  

E-Print Network [OSTI]

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

Yeamans, Charles Burnett, 1978-

2003-01-01T23:59:59.000Z

260

SHEEP MOUNTAIN URANIUM PROJECT CROOKS GAP, WYOMING  

E-Print Network [OSTI]

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

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


261

Uranium(VI) extraction by TBP in the presence of HDBP  

SciTech Connect (OSTI)

The influence of di-n-butyl phosphoric acid (HDBP) upon extraction of uranium(VI) by tri-n-butyl phosphate (TBP) from 0.5--3.0 M nitric acid solutions has been studied. It has been shown that the uranium(VI) distribution coefficient D{sub U} for extraction by 1.1 M TBP in tri-decane or xylene is increased when HDBP is present in the organic phase. For iso-molar solutions of (TBP + HDBP) with a total concentration of 0.36 M, and Uranium(VI) aqueous concentration up to 10--20 g/l, a maximum value of D{sub U} is observed when TBP/HDBP = 1; for higher U(VI) concentration the maximum gradually disappears, with D{sub U} growing monotonically with the HDBP content in the organic phase. Uranium(VI) absorption spectra for 1.1 M TBP in tri-decane or xylene, containing HDBP, provide evidence for the formation of compounds, of which composition is intermediate between uranyl nitrate--TBP disolvate and the U(VI)--HDBP complex. It is proposed that these intermediate compounds are UO{sub 2}(NO{sub 3}){sub 2}HDBP.TBP and UO{sub 2}(NO{sub 3}){sub 2}(HDBP){sub 2}.

Fedorov, Yu.S.; Zilberman, B.Ya.; Kulikov, S.M.; Blazheva, I.V.; Mishin, E.N. [V.G. Khlopin Radium Inst., Saint-Petersburg (Russian Federation); Wallwork, A.L.; Denniss, I.S.; May, I. [British Nuclear Fuels plc, Sellafield (United Kingdom); Hill, N.J. [British Nuclear Fuels plc, Risley (United Kingdom)

1999-03-01T23:59:59.000Z

262

Review of uranium bioassay techniques  

SciTech Connect (OSTI)

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

Bogard, J.S.

1996-04-01T23:59:59.000Z

263

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

SciTech Connect (OSTI)

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

Cantrell, J.

2012-05-23T23:59:59.000Z

264

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

E-Print Network [OSTI]

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

Meyer, Karsten

265

Electric Turbo Compounding Technology Update  

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

Turbo Compounding Technology Update Electric Turbo Compounding Technology Update 15 August, 2007 Carl Vuk 15 August, 2007 Carl Vuk Electric Turbo Compounding Highlights Electric...

266

Statistical data of the uranium industry  

SciTech Connect (OSTI)

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

none,

1982-01-01T23:59:59.000Z

267

Adsorptive Stripping Voltammetric Measurements of Trace Uranium...  

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

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

268

Biogeochemical Processes In Ethanol Stimulated Uranium Contaminated...  

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

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

269

Colorimetric detection of uranium in water  

DOE Patents [OSTI]

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

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

2012-03-13T23:59:59.000Z

270

Uranium Weapons Components Successfully Dismantled | National...  

National Nuclear Security Administration (NNSA)

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

271

High strength and density tungsten-uranium alloys  

DOE Patents [OSTI]

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

Sheinberg, Haskell (Los Alamos, NM)

1993-01-01T23:59:59.000Z

272

Distribution of uranium-bearing phases in soils from Fernald  

SciTech Connect (OSTI)

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

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

1993-12-31T23:59:59.000Z

273

Finding of No Significant Impact, proposed remediation of the Maybell Uranium Mill Processing Site, Maybell, Colorado  

SciTech Connect (OSTI)

The U.S. Department of Energy (DOE) has prepared an environmental assessment (EA) (DOE/EA-0347) on the proposed surface remediation of the Maybell uranium mill processing site in Moffat County, Colorado. The mill site contains radioactively contaminated materials from processing uranium ore that would be stabilized in place at the existing tailings pile location. Based on the analysis in the EA, DOE has determined that the proposed action does not constitute a major federal action significantly affecting the quality of the human environment within the meaning of the National Environmental Policy Act (NEPA) of 1969, Public Law 91-190 (42 U.S.C. {section}4321 et seq.), as amended. Therefore, preparation of an environmental impact statement is not required and DOE is issuing this Finding of No Significant Impact (FONSI).

Not Available

1995-12-31T23:59:59.000Z

274

Cleanup of inactive Uranium Mill Tailings Sites in the Navajo Nation  

SciTech Connect (OSTI)

The U.S. Congress passed the Uranium Mill Tailings Radiation Control Act (UMTRCA) in 1978 to address potential and significant radiation health hazards to the public from active and inactive mill operations. Title I to the UMTRCA identified sites to be designated for remedial action. These include four uranium mill tailings remedial action (UMTRA) sites in the Navajo Nation. These sites are located in Shiprock, New Mexico; Tuba City, Arizona; Cane Valley, Arizona; and Halchita, Utah. The U.S. Department of Energy (DOE) was directed to select and execute a plan of remedial action that provides long-term stabilization and control of radioactive materials and satisfies the U.S. Environmental Protection Agency standards and other applicable laws and regulations.

Martin, B.

1994-12-31T23:59:59.000Z

275

How much Uranium is in the Earth? Predictions for geo-neutrinos at KamLAND  

E-Print Network [OSTI]

Geo-neutrino detection can determine the amount of long-lived radioactive elements within our planet, thus providing a direct test of the Bulk Silicate Earth (BSE) model and fixing the radiogenic contribution to the terrestrial heat. We present a prediction for the geo-neutrino signal at KamLAND as a function of the Uranium mass in the Earth. The prediction is based on global mass balance, supplemented by a detailed geochemical and geophysical study of the region near the detector. The prediction is weakly dependent on mantle modeling. If BSE is correct, Uranium geo-neutrinos will produce between 25 and 35 events per year and 10^32 protons at Kamioka.

Gianni Fiorentini; Marcello Lissia; Fabio Mantovani; Riccardo Vannucci

2005-08-04T23:59:59.000Z

276

Radioactive decay data tables  

SciTech Connect (OSTI)

The estimation of radiation dose to man from either external or internal exposure to radionuclides requires a knowledge of the energies and intensities of the atomic and nuclear radiations emitted during the radioactive decay process. The availability of evaluated decay data for the large number of radionuclides of interest is thus of fundamental importance for radiation dosimetry. This handbook contains a compilation of decay data for approximately 500 radionuclides. These data constitute an evaluated data file constructed for use in the radiological assessment activities of the Technology Assessments Section of the Health and Safety Research Division at Oak Ridge National Laboratory. The radionuclides selected for this handbook include those occurring naturally in the environment, those of potential importance in routine or accidental releases from the nuclear fuel cycle, those of current interest in nuclear medicine and fusion reactor technology, and some of those of interest to Committee 2 of the International Commission on Radiological Protection for the estimation of annual limits on intake via inhalation and ingestion for occupationally exposed individuals.

Kocher, D.C.

1981-01-01T23:59:59.000Z

277

Transmutation of high-level radioactive waste - Perspectives  

E-Print Network [OSTI]

In a fast neutron spectrum essentially all long-lived actinides (e.g. Plutonium) undergo fission and thus can be transmuted into generally short lived fission products. Innovative nuclear reactor concepts e.g. accelerator driven systems (ADS) are currently in development that foresee a closed fuel cycle. The majority of the fissile nuclides (uranium, plutonium) shall be used for power generation and only fission products will be put into final disposal that needs to last for a historical time scale of only 1000 years. For the transmutation of high-level radioactive waste a lot of research and development is still required. One aspect is the precise knowledge of nuclear data for reactions with fast neutrons. Nuclear reactions relevant for transmutation are being investigated in the framework of the european project ERINDA. First results from the new neutron time-of-flight facility nELBE at Helmholtz-Zentrum Dresden-Rossendorf will be presented.

Junghans, Arnd; Grosse, Eckart; Hannaske, Roland; Kgler, Toni; Massarczyk, Ralf; Schwengner, Ronald; Wagner, Andreas

2014-01-01T23:59:59.000Z

278

President Truman Increases Production of Uranium and Plutonium...  

National Nuclear Security Administration (NNSA)

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

279

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

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

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

280

Toxic Substances Control Act Uranium Enrichment Federal Facility...  

Office of Environmental Management (EM)

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

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


281

Geochemical Controls on Contaminant Uranium in Vadose Hanford...  

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

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

282

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

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

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

283

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

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

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

284

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

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

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

285

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

Energy Savers [EERE]

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

286

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

Energy Savers [EERE]

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

287

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

Office of Environmental Management (EM)

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

288

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

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

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

289

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

Office of Environmental Management (EM)

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

290

Microsoft Word - Workers Demolishing Last Inactive Facility at...  

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

structure contaminated with asbestos and a low-level radioactive chemical compound called uranium hexafluoride (UF 6 ). With an original footprint of almost five acres - roughly...

291

Geochemical information for sites contaminated with low-level radioactive wastes: II. St. Louis Airport Storage Site  

SciTech Connect (OSTI)

The St. Louis Airport Storage Site (SLASS) became radioactively contaminated as a result of wastes that were being stored from operations to recover uranium from pitchblende ores in the 1940s and 1950s. The US Department of Energy is considering various remedial action options for the SLASS under the Formerly Utilized Site Remedial Action Program (FUSRAP). This report describes the results of geochemical investigations, carried out to support the FUSRAP activities and to aid in quantifying various remedial action options. Soil and groundwater samples from the site were characterized, and sorption ratios for uranium and radium and apparent concentration limit values for uranium were measured in soil/groundwater systems by batch contact methodology. The uranium and radium concentrations in soil samples were significantly above background near the old contaminated surface horizon (now at the 0.3/sup -/ to 0.9/sup -/m depth); the maximum values were 1566 ..mu..g/g and 101 pCi/g, respectively. Below about the 6/sup -/m depth, the concentrations appeared to be typical of those naturally present in soils of this area (3.8 +- 1.2 ..mu..g/g and 3.1 +- 0.6 pCi/g). Uranium sorption ratios showed stratigraphic trends but were generally moderate to high (100 to 1000 L/kg). The sorption isotherm suggested an apparent uranium concentration limit of about 200 mg/L. This relatively high solubility can probably be correlated with the carbonate content of the soil/groundwater systems. The lower sorption ratio values obtained from the sorption isotherm may have resulted from changes in the experimental procedure or the groundwater used. The SLASS appears to exhibit generally favorable behavior for the retardation of uranium solubilized from waste in the site. Parametric tests were conducted to estimate the sensitivity of uranium sorption and solubility to the pH and carbonate content of the system.

Seeley, F.G.; Kelmers, A.D.

1985-01-01T23:59:59.000Z

292

Radioactive waste material melter apparatus  

DOE Patents [OSTI]

An apparatus for preparing metallic radioactive waste material for storage is disclosed. The radioactive waste material is placed in a radiation shielded enclosure. The waste material is then melted with a plasma torch and cast into a plurality of successive horizontal layers in a mold to form a radioactive ingot in the shape of a spent nuclear fuel rod storage canister. The apparatus comprises a radiation shielded enclosure having an opening adapted for receiving a conventional transfer cask within which radioactive waste material is transferred to the apparatus. A plasma torch is mounted within the enclosure. A mold is also received within the enclosure for receiving the melted waste material and cooling it to form an ingot. The enclosure is preferably constructed in at least two parts to enable easy transport of the apparatus from one nuclear site to another.

Newman, Darrell F. (Richland, WA); Ross, Wayne A. (Richland, WA)

1990-01-01T23:59:59.000Z

293

Radioactive waste material melter apparatus  

DOE Patents [OSTI]

An apparatus for preparing metallic radioactive waste material for storage is disclosed. The radioactive waste material is placed in a radiation shielded enclosure. The waste material is then melted with a plasma torch and cast into a plurality of successive horizontal layers in a mold to form a radioactive ingot in the shape of a spent nuclear fuel rod storage canister. The apparatus comprises a radiation shielded enclosure having an opening adapted for receiving a conventional transfer cask within which radioactive waste material is transferred to the apparatus. A plasma torch is mounted within the enclosure. A mold is also received within the enclosure for receiving the melted waste material and cooling it to form an ingot. The enclosure is preferably constructed in at least two parts to enable easy transport of the apparatus from one nuclear site to another. 8 figs.

Newman, D.F.; Ross, W.A.

1990-04-24T23:59:59.000Z

294

XAFS Model Compound Library  

DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

The XAFS Model Compound Library contains XAFS data on model compounds. The term "model" compounds refers to compounds of homogeneous and well-known crystallographic or molecular structure. Each data file in this library has an associated atoms.inp file that can be converted to a feff.inp file using the program ATOMS. (See the related Searchable Atoms.inp Archive at http://cars9.uchicago.edu/~newville/adb/) This Library exists because XAFS data on model compounds is useful for several reasons, including comparing to unknown data for "fingerprinting" and testing calculations and analysis methods. The collection here is currently limited, but is growing. The focus to date has been on inorganic compounds and minerals of interest to the geochemical community. [Copied, with editing, from http://cars9.uchicago.edu/~newville/ModelLib/

Newville, Matthew

295

Storage depot for radioactive material  

DOE Patents [OSTI]

Vertical drilling of cylindrical holes in the soil, and the lining of such holes, provides storage vaults called caissons. A guarded depot is provided with a plurality of such caissons covered by shielded closures preventing radiation from penetrating through any linear gap to the atmosphere. The heat generated by the radioactive material is dissipated through the vertical liner of the well into the adjacent soil and thus to the ground surface so that most of the heat from the radioactive material is dissipated into the atmosphere in a manner involving no significant amount of biologically harmful radiation. The passive cooling of the radioactive material without reliance upon pumps, personnel, or other factor which might fail, constitutes one of the most advantageous features of this system. Moreover this system is resistant to damage from tornadoes or earthquakes. Hermetically sealed containers of radioactive material may be positioned in the caissons. Loading vehicles can travel throughout the depot to permit great flexibility of loading and unloading radioactive materials. Radioactive material can be shifted to a more closely spaced caisson after ageing sufficiently to generate much less heat. The quantity of material stored in a caisson is restricted by the average capacity for heat dissipation of the soil adjacent such caisson.

Szulinski, Milton J. (Richland, WA)

1983-01-01T23:59:59.000Z

296

Petrochemical and Mineralogical Constraints on the Source and Processes of Uranium Mineralisation in the Granitoids of Zing-Monkin Area, Adamawa Massif, NE Nigeria  

SciTech Connect (OSTI)

Zing-Monkin area, located in the northern part of Adamawa Massif, is underlain by extensive exposures of moderately radioactive granodiorites, anatectic migmatites, equigranular granites, porphyritic granites and highly radioactive fine-grained granites with minor pegmatites. Selected major and trace element petrochemical investigations of the rocks show that a progression from granodiorite through migmatite to granites is characterised by depletion of MgO, CaO, Fe{sub 2}O{sub 3,} Sr, Ba, and Zr, and enrichment of SiO{sub 2} and Rb. This trend is associated with uranium enrichment and shows a chemical gradation from the more primitive granodiorite to the more evolved granites. Electron microprobe analysis shows that the uranium is content in uranothorite and in accessories, such as monazite, titanite, apatite, epidote and zircon. Based on petrochemical and mineralogical data, the more differentiated granitoids (e.g., fine-grained granite) bordering the Benue Trough are the immediate source of the uranium prospect in Bima Sandstone within the Trough. Uranium was derived from the granitoids by weathering and erosion. Transportation and subsequent interaction with organic matter within the Bima Sandstone led to precipitation of insoluble secondary uranium minerals in the Benue Trough.

Haruna, I. V., E-mail: vela_hi@yahoo.co.uk [Federal University of Technology, Geology Department (Nigeria); Orazulike, D. M. [Abubakar Tafawa Balewa University, Geology Programme (Nigeria); Ofulume, A. B. [Federal University of Technology, Geosciences Department (Nigeria); Mamman, Y. D. [Federal University of Technology, Geology Department (Nigeria)

2011-12-15T23:59:59.000Z

297

Partially fluorinated ionic compounds  

DOE Patents [OSTI]

Partially fluorinated ionic compounds are prepared. They are useful in the preparation of partially fluorinated dienes, in which the repeat units are cycloaliphatic.

Han, legal representative, Amy Qi (Hockessin, DE); Yang, Zhen-Yu (Hockessin, DE)

2008-11-25T23:59:59.000Z

298

Baseline risk assessment of ground water contamination at the uranium mill tailings site near Canonsburg, Pennsylvania. Revision 1  

SciTech Connect (OSTI)

For the UMTRA Project site located near Canonsburg, Pennsylvania (the Canonsburg site), the Surface Project cleanup occurred from 1983 to 1985, and involved removing the uranium processing mill tailings and radioactively contaminated soils and materials from their original locations and placing them in a disposal cell located on the former Canonsburg uranium mill site. This disposal cell is designed to minimize radiation emissions and further contamination of ground water beneath the site. The Ground Water Project will evaluate the nature and the extent of ground water contamination resulting from uranium processing at the former Canonsburg uranium mill site, and will determine a ground water strategy for complying with the US Environmental Protection Agency`s (EPA) ground water standards established for the UMTRA Project. For the Canonsburg site, an evaluation was made to determine whether exposure to ground water contaminated by uranium processing could affect people`s health. This risk assessment report is the first site-specific document prepared for the UMTRA Ground Water Project at the Canonsburg site. The results of this report and further site characterization of the Canonsburg site will be used to determine how to protect public health and the environment, and how to comply with the EPA standards.

NONE

1995-11-01T23:59:59.000Z

299

National low-level waste management program radionuclide report series, Volume 15: Uranium-238  

SciTech Connect (OSTI)

This report, Volume 15 of the National Low-Level Waste Management Program Radionuclide Report Series, discusses the radiological and chemical characteristics of uranium-238 ({sup 238}U). The purpose of the National Low-Level Waste Management Program Radionuclide Report Series is to provide information to state representatives and developers of low-level radioactive waste disposal facilities about the radiological, chemical, and physical characteristics of selected radionuclides and their behavior in the waste disposal facility environment. This report also includes discussions about waste types and forms in which {sup 238}U can be found, and {sup 238}U behavior in the environment and in the human body.

Adams, J.P.

1995-09-01T23:59:59.000Z

300

Bioremediation of uranium contaminated soils and wastes  

SciTech Connect (OSTI)

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

Francis, A.J.

1998-12-31T23:59:59.000Z

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


301

Uranium Management - Preservation of a National Asset  

SciTech Connect (OSTI)

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

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

2002-02-27T23:59:59.000Z

302

Removal of Historic Low-Level Radioactive Sediment from the Port Hope Harbour - 13314  

SciTech Connect (OSTI)

At the Port Hope Harbour, located on the north shore of Lake Ontario, the presence of low-level radioactive sediment, resulting from a former radium and uranium refinery that operated alongside the Harbour, currently limits redevelopment and revitalization opportunities. These waste materials contain radium-226, uranium, arsenic and other contaminants. Several other on-land locations within the community of Port Hope are also affected by the low-level radioactive waste management practices of the past. The Port Hope Project is a community initiated undertaking that will result in the consolidation of an estimated 1.2 million cubic metres of the low-level radioactive waste from the various sites in Port Hope into a new engineered above ground long-term waste management facility. The remediation of the estimated 120,000 m{sup 3} of contaminated sediments from the Port Hope Harbour is one of the more challenging components of the Port Hope Project. Following a thorough review of various options, the proposed method of contaminated sediment removal is by dredging. The sediment from the dredge will then be pumped as a sediment-water slurry mixture into geo-synthetic containment tubes for dewatering. Due to the hard substrate below the contaminated sediment, the challenge has been to set performance standards in terms of low residual surface concentrations that are attainable in an operationally efficient manner. (authors)

Kolberg, Mark [Baird and Associates, 1267 Cornwall Rd., Suite 100, Oakville ON, L6J7T5 (Canada)] [Baird and Associates, 1267 Cornwall Rd., Suite 100, Oakville ON, L6J7T5 (Canada); Case, Glenn [Atomic Energy of Canada Limited, Port Hope, ON (Canada)] [Atomic Energy of Canada Limited, Port Hope, ON (Canada); Ferguson Jones, Andrea [MMM Group Limited, Thornhill, ON (Canada)] [MMM Group Limited, Thornhill, ON (Canada)

2013-07-01T23:59:59.000Z

303

IPNS enriched uranium booster target  

SciTech Connect (OSTI)

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

Schulke, A.W. Jr.

1985-01-01T23:59:59.000Z

304

Impact assessment of draft DOE Order 5820.2B. Radioactive Waste Technical Support Program  

SciTech Connect (OSTI)

The Department of Energy (DOE) has prepared a revision to DOE Order 5820.2A, entitled ``Radioactive Waste Management.`` DOE issued DOE Order 5820.2A in September 1988 and, as the title implies, it covered only radioactive waste forms. The proposed draft order, entitled ``Waste Management,`` addresses the management of both radioactive and nonradioactive waste forms. It also includes spent nuclear fuel, which DOE does not consider a waste. Waste forms covered include hazardous waste, high-level waste, transuranic (TRU) waste, low-level radioactive waste, uranium and thorium mill tailings, mixed waste, and sanitary waste. The Radioactive Waste Technical Support Program (TSP) of Leached Idaho Technologies Company (LITCO) is facilitating the revision of this order. The EM Regulatory Compliance Division (EM-331) has requested that TSP estimate the impacts and costs of compliance with the revised order. TSP requested Dames & Moore to aid in this assessment by comparing requirements in Draft Order 5820.2B to ones in DOE Order 5820.2A and other DOE orders and Federal regulations. The assessment started with a draft version of 5820.2B dated January 14, 1994. DOE has released three updated versions of the draft order since then (dated May 20, 1994; August 26, 1994; and January 23, 1995). Each time DOE revised the order, Dames and Moore updated the assessment work to reflect the text changes. This report reflects the January 23, 1995 version of the draft order.

NONE

1995-04-01T23:59:59.000Z

305

Integrated data base report - 1994: US spent nuclear fuel and radioactive waste inventories, projections, and characteristics  

SciTech Connect (OSTI)

The Integrated Data Base Program has compiled historic data on inventories and characteristics of both commercial and U.S. Department of Energy (DOE) spent nuclear fuel and commercial and U.S. government-owned radioactive wastes. Except for transuranic wastes, inventories of these materials are reported as of December 31, 1994. Transuranic waste inventories are reported as of December 31, 1993. All spent nuclear fuel and radioactive waste data reported are based on the most reliable information available from government sources, the open literature, technical reports, and direct contacts. The information forecasted is consistent with the latest DOE/Energy Information Administration (EIA) projections of U.S. commercial nuclear power growth and the expected DOE-related and private industrial and institutional activities. The radioactive materials considered, on a chapter-by-chapter basis, are spent nuclear fuel, high-level waste, transuranic waste, low-level waste, commercial uranium mill tailings, DOE Environmental Restoration Program contaminated environmental media, commercial reactor and fuel-cycle facility decommissioning wastes, and mixed (hazardous and radioactive) low-level waste. For most of these categories, current and projected inventories are given through the calendar-year 2030, and the radioactivity and thermal power are calculated based on reported or estimated isotopic compositions.

NONE

1995-09-01T23:59:59.000Z

306

Molten-Salt Depleted-Uranium Reactor  

E-Print Network [OSTI]

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

Dong, Bao-Guo; Gu, Ji-Yuan

2015-01-01T23:59:59.000Z

307

Method for fabricating laminated uranium composites  

DOE Patents [OSTI]

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

Chapman, L.R.

1983-08-03T23:59:59.000Z

308

National Uranium Resource Evaluation, Tonopah quadrangle, Nevada  

SciTech Connect (OSTI)

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

Hurley, B W; Parker, D P

1982-04-01T23:59:59.000Z

309

Uranium in prehistoric Indian pottery  

E-Print Network [OSTI]

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

Filberth, Ernest William

2012-06-07T23:59:59.000Z

310

2013 Uranium Marketing Annual Report  

Gasoline and Diesel Fuel Update (EIA)

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

311

2013 Uranium Marketing Annual Report  

Gasoline and Diesel Fuel Update (EIA)

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

312

2013 Uranium Marketing Annual Report  

Gasoline and Diesel Fuel Update (EIA)

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

313

2013 Uranium Marketing Annual Report  

Gasoline and Diesel Fuel Update (EIA)

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

314

2013 Uranium Marketing Annual Report  

Gasoline and Diesel Fuel Update (EIA)

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

315

U.S.Uranium Reserves  

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

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

316

2013 Uranium Marketing Annual Report  

U.S. Energy Information Administration (EIA) Indexed Site

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data CenterFranconia, Virginia:FAQ < RAPID Jump to:SeadovCooperativeA2. World liquids consumption by region,Purchases2 U.S.Feed6a. Uranium

317

2013 Uranium Marketing Annual Report  

U.S. Energy Information Administration (EIA) Indexed Site

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data CenterFranconia, Virginia:FAQ < RAPID Jump to:SeadovCooperativeA2. World liquids consumption by region,Purchases2 U.S.Feed6a.4. Uranium

318

Studies of the mobility of uranium and thorium in Nevada Test Site tuff  

SciTech Connect (OSTI)

Hydro-geochemical processes must be understood if the movement of radionuclides away from a breached radioactive waste canister is to be modeled and predicted. In this respect, occurrences of uranium and thorium in hydrothermal systems are under investigation in tuff and in rhyolitic tuff that was heated to simulate the effects of introduction of radioactive waste. In these studies, high-resolution gamma spectrometry and fission-track radiography are coupled with observations of alteration mineralogy and thermal history to deduce the evidence of, or potential for movement of, U and Th in response to the thermal environment. Observations to date suggest that U was mobile in the vicinity of the heater but that localized reducing environments provided by Fe-Ti-Mn-oxide minerals concentrated U and thus attenuated its migration.

Wollenberg, H.A.; Flexser, S.; Smith, A.R. [Lawrence Berkeley Lab., CA (United States)

1991-06-01T23:59:59.000Z

319

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

SciTech Connect (OSTI)

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

Francis, C. W.

1993-09-01T23:59:59.000Z

320

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

SciTech Connect (OSTI)

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

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

1995-12-31T23:59:59.000Z

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


321

Uranium Cluster Chemistry DOI: 10.1002/anie.200906605  

E-Print Network [OSTI]

Uranium Cluster Chemistry DOI: 10.1002/anie.200906605 Tetranuclear Uranium Clusters by Reductive in the coordination chemistry and small-molecule reactivity of uranium. Among the intriguing reactivity patterns of tetravalent uranium with 3,5-dimethylpyrazolate (Me2Pz? ) led to forma- tion of an unprecedented homoleptic

322

Regional impacts of uranium mining and milling employment decline: a preliminary appraisal  

SciTech Connect (OSTI)

The purpose of this report is to identify counties that have been significantly impacted by declining uranium employment and to gauge the relative severity of impacts upon different counties given the differing compositions of their economic bases. Colorado, New Mexico, Texas, Utah, and Wyoming have been identified as major uranium mining and milling states. Twenty-four major uranium mining and milling counties within these states lost an estimated total of 9400 jobs between 1980 and 1983 following the 1980 peak employment of approximately 15,700. Economic profiles for these 24 counties were prepared using an historical employment data base containing annual employment data for major economic sectors 1970 through 1983. Additionally, regression analysis was used to derive a mining employment impact multiplier of 2.5. This means that for every mining job lost, an additional 1.5 jobs are lost in the service sector. The historical growth experiences in other economic sectors for 16 of these counties have been such that the counties are unlikely to regain the lost uranium mining and milling jobs through growth in other basic employment sectors. These counties may experience an additional loss of 12.2 thousand service sector jobs through the multiplier effect of basic sector employment loss. The other eight uranium-producing counties should have sufficient growth opportunities in other basic sectors to enable them to retain existing service sector jobs. However, economic growth in these counties may not be as great as it would have been had the counties not lost the uranium employment. For both sets of counties, the downturn in the national economy in the early 1980s has compounded the local employment problem. 22 refs., 6 figs., 12 tabs.

Vogt, D.P.; Rizy, C.G.; Watson, R.A.

1985-07-01T23:59:59.000Z

323

Electrostatics and radioactive aerosol behavior  

SciTech Connect (OSTI)

Radioactive aerosols differ from their nonradioactive counterparts by their ability to charge themselves by emitting charged particles during the radioactive decay process. Evidence that electrostatics, including this charging process, can affect the transport of the aerosols was summarized previously. Charge distributions and the mean charge for a monodisperse radioactive aerosol have been considered in detail. The principal results of theory to calculate charge distributions on a aerosol with a size distribution, changes to Brownian coagulation rates for an aerosol in a reactor containment, and possible changes to aerosol deposition resulting from the charging will be presented. The main purpose of the work has been to improve calculations of aerosol behavior in reactor containments, but behavior in less ionizing environments will be affected more strongly, and some problems remain to be solved in performing reliable calculations.

Clement, C.F.

1994-12-31T23:59:59.000Z

324

Technical Basis for Assessing Uranium Bioremediation Performance  

SciTech Connect (OSTI)

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

PE Long; SB Yabusaki; PD Meyer; CJ Murray; AL NGuessan

2008-04-01T23:59:59.000Z

325

Storage containers for radioactive material  

DOE Patents [OSTI]

A radioactive material storage system for use in the laboratory having a flat base plate with a groove in one surface thereof and a hollow pedestal extending perpendicularly away from the other surface thereof, a sealing gasket in the groove, a cover having a filter therein and an outwardly extending flange which fits over the plate, the groove and the gasket, and a clamp for maintaining the cover and the plate sealed together, whereby the plate and the cover and the clamp cooperate to provide a storage area for radioactive material readily accessible for use or

Groh, Edward F. (Naperville, IL); Cassidy, Dale A. (Valparaiso, IN); Dates, Leon R. (Elmwood Park, IL)

1981-01-01T23:59:59.000Z

326

Storage containers for radioactive material  

DOE Patents [OSTI]

A radioactive material storage system is claimed for use in the laboratory having a flat base plate with a groove in one surface thereof and a hollow pedestal extending perpendicularly away from the other surface thereof, a sealing gasket in the groove, a cover having a filter therein and an outwardly extending flange which fits over the plate, the groove and the gasket, and a clamp for maintaining the cover and the plate sealed together. The plate and the cover and the clamp cooperate to provide a storage area for radioactive material readily accessible for use or inventory. Wall mounts are provided to prevent accidental formation of critical masses during storage.

Groh, E.F.; Cassidy, D.A.; Dates, L.R.

1980-07-31T23:59:59.000Z

327

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

E-Print Network [OSTI]

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

Duhovic, Selma

2012-01-01T23:59:59.000Z

328

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

E-Print Network [OSTI]

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

Rao, Linfeng

2011-01-01T23:59:59.000Z

329

Electrolytic process for preparing uranium metal  

DOE Patents [OSTI]

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

Haas, Paul A. (Knoxville, TN)

1990-01-01T23:59:59.000Z

330

Capstone Depleted Uranium Aerosols: Generation and Characterization  

SciTech Connect (OSTI)

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

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

2004-10-19T23:59:59.000Z

331

Heart testing compound  

DOE Patents [OSTI]

The compound 15-(p-[.sup.125 I]-iodophenyl)-6-tellurapentadecanoic acid is disclosed as a myocardial imaging agent having rapid and pronounced uptake, prolonged myocardial retention, and low in vivo deiodination.

Knapp, Jr., Furn F. (Oak Ridge, TN); Goodman, Mark M. (Knoxville, TN)

1985-01-01T23:59:59.000Z

332

Heart testing compound  

DOE Patents [OSTI]

The compound 15-(p-(/sup 125/I)-iodophenyl)-6-tellurapentadecanoic acid is disclosed as a myocardial imaging agent having rapid and pronounced uptake, prolonged myocardial retention, and low in vivo deiodination.

Knapp, F.F. Jr.; Goodman, M.M.

1983-06-29T23:59:59.000Z

333

EA-1599: Disposition of Radioactively Contaminated Nickel Located at the East Tennessee Technology Park, Oak Ridge, Tennessee, and the Paducah Gaseous Diffusion Plant, Paducah, Kentucky, for Controlled Radiological Applications  

Broader source: Energy.gov [DOE]

This EA was being prepared to evaluate potential environmental impacts of a proposal to dispose of nickel scrap that is volumetrically contaminated with radioactive materials and that DOE recovered from equipment it had used in uranium enrichment. This EA is on hold.

334

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

E-Print Network [OSTI]

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

Sigmon, Ginger E.

2010-01-01T23:59:59.000Z

335

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

E-Print Network [OSTI]

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

Geiler, Andrea

2007-01-01T23:59:59.000Z

336

The Radioactive Beam Program at Argonne  

E-Print Network [OSTI]

In this talk I will present selected topics of the ongoing radioactive beam program at Argonne and discuss the capabilities of the CARIBU radioactive ion production facility as well as plans for construction of a novel superconducting solenoid spectrometer.

B. B. Back

2006-06-06T23:59:59.000Z

337

Low Level Radioactive Waste Authority (Michigan)  

Broader source: Energy.gov [DOE]

Federal laws passed in 1980 and 1985 made each state responsible for the low-level radioactive waste produced within its borders. Act 204 of 1987 created the Low-Level Radioactive Waste Authority ...

338

Internal and External Radioactive Backgrounds  

E-Print Network [OSTI]

Chapter 3 Internal and External Radioactive Backgrounds New physics is often discovered by pushing energies. With the current large mixing angle-MSW oscillation parameters, Borexino expects to observe 0.35 neutrino events per day per ton from 7Be in the energy window. Because there are so few events

339

SRP RADIOACTIVE WASTE RELEASES S  

Office of Scientific and Technical Information (OSTI)

. . . . . -- SRP RADIOACTIVE WASTE RELEASES S t a r t u p t h r o u g h 1 9 5 9 September 1 9 6 0 - R E C O R D - W O R K S T E C H N I C A L D E P A R T M E N T 1 J. E. C o l e ,...

340

Reporting of Radioactive Sealed Sources  

Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

To establish U.S. Department of Energy requirements for inventory reporting, transaction reporting, verification of reporting, and assign responsibilities for reporting of radioactive sealed sources. DOE N 251.86 extends this notice until 5-6-11. No cancellations. Canceled by DOE O 231.1B

2008-02-27T23:59:59.000Z

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


341

(Revised May 25, 2012) Radioactivity  

E-Print Network [OSTI]

(Revised May 25, 2012) Radioactivity GOALS (1) To gain a better understanding of naturally-occurring. (3) To measure the amount of "background radiation" from natural sources. (4) To test whether and man-made radiation sources. (2) To use a Geiger-Mueller tube to detect both beta and gamma radiation

Collins, Gary S.

342

LITERATURE SURVEY FOR GROUNDWATER TREATMENT OPTIONS FOR NITRATE IODINE-129 AND URANIUM 200-ZP-1 OPERABLE UNIT HANFORD SITE  

SciTech Connect (OSTI)

This literature review presents treatment options for nitrate, iodine-129, and uranium, which are present in groundwater at the 200-ZP-I Groundwater Operable Unit (OU) within the 200 West Area of the Hanford Site. The objective of this review is to determine available methods to treat or sequester these contaminants in place (i.e., in situ) or to pump-and-treat the groundwater aboveground (i.e., ex situ). This review has been conducted with emphasis on commercially available or field-tested technologies, but theoretical studies have, in some cases, been considered when no published field data exist. The initial scope of this literature review included only nitrate and iodine-I 29, but it was later expanded to include uranium. The focus of the literature review was weighted toward researching methods for treatment of nitrate and iodine-129 over uranium because of the relatively greater impact of those compounds identified at the 200-ZP-I OU.

BYRNES ME

2008-06-05T23:59:59.000Z

343

Characterization of Uranium Codeposited with Hydrogen on Nickel Cathodes  

SciTech Connect (OSTI)

Previously, it has been reported that nuclear transmutation reactions are accelerated when radioactive elements are subjected to low-level electric fields during electrolysis of aqueous electrolytes. Our research investigated the codeposition of U{sub 3}O{sub 8} and H on Ni cathodes, using an acidic electrolyte and a Pt anode. Then, the radiation emitted by the electroplated U{sub 3}O{sub 8} was compared with radiation emitted by unelectrolyzed U{sub 3}O{sub 8} from the same batch. The electroplated U{sub 3}O{sub 8} initially produced {approx}2900 counts in 3 min (April 17, 2000). This rose sporadically in steps to {approx} 3700 counts in 3 min on May 11, 2000, and it remained relatively constant at this level until the GM measurements ended on June 8, 2000. The unelectrolyzed U{sub 3}O{sub 8} from the same batch emitted radiation at a much lower rate, {approx}1250 counts in 3 min, and this remained almost constant over the entire period of measurement. After the GM measurements, a gamma-ray spectrometer was used to measure radiation from the same two, 10-mg electroplated and unelectrolyzed U{sub 3}O{sub 8} samples. The net integral of the same 36 peaks for the same measurement time (25 h) gave 53 000 counts for the electroplated sample, 1.7 times as many as the 31 000 counts for the unelectrolyzed sample. Alpha and beta measurements are under way for both samples. Figure 2 shows a scanning electron microscope micrograph of a typical surface structure of uranium electroplated on a nickel cathode. The donut-like features appear to be the result of microscopic surface eruptions that produced voids surrounded by raised circular rims. Figure 3 shows an energy dispersive spectrometer spectrum from electroplated U{sub 3}O{sub 8} on a nickel cathode. In addition to oxygen and uranium, cesium, iron, and nickel are present. A peak at 16.36 keV, which overlaps with a uranium peak at 16.44 keV, is tentatively labeled as fermium. Mass spectrometer and X-ray diffraction studies are also underway.

G. Goddard; S. Frantz

2000-11-12T23:59:59.000Z

344

MILDOS - A Computer Program for Calculating Environmental Radiation Doses from Uranium Recovery Operations  

SciTech Connect (OSTI)

The MILDOS Computer Code estimates impacts from radioactive emissions from uranium milling facilities. These impacts are presented as dose commitments to individuals and the regional population within an 80 km radius of the facility. Only airborne releases of radioactive materials are considered: releases to surface water and to groundwater are not addressed in MILDOS. This code is multi-purposed and can be used to evaluate population doses for NEPA assessments, maximum individual doses for predictive 40 CFR 190 compliance evaluations, or maximum offsite air concentrations for predictive evaluations of 10 CFR 20 compliance. Emissions of radioactive materials from fixed point source locations and from area sources are modeled using a sector-averaged Gaussian plume dispersion model, which utilizes user-provided wind frequency data. Mechanisms such as deposition of particulates, resuspension. radioactive decay and ingrowth of daughter radionuclides are included in the transport model. Annual average air concentrations are computed, from which subsequent impacts to humans through various pathways are computed. Ground surface concentrations are estimated from deposition buildup and ingrowth of radioactive daughters. The surface concentrations are modified by radioactive decay, weathering and other environmental processes. The MILDOS Computer Code allows the user to vary the emission sources as a step function of time by adjustinq the emission rates. which includes shutting them off completely. Thus the results of a computer run can be made to reflect changing processes throughout the facility's operational lifetime. The pathways considered for individual dose commitments and for population impacts are: Inhalation External exposure from ground concentrations External exposure from cloud immersion Ingestioo of vegetables Ingestion of meat Ingestion of milk Dose commitments are calculated using dose conversion factors, which are ultimately based on recommendations of the International Commission on Radiological Protection (ICRP). These factors are fixed internally in the code, and are not part of the input option. Dose commitments which are available from the code are as follows: Individual dose commitments for use in predictive 40 CFR 190 compliance evaluations (Radon and short-lived daughters are excluded) Total individual dose commitments (impacts from all available radionuclides are considered) Annual population dose commitments (regional, extraregional, total and cummulative). This model is primarily designed for uranium mill facilities, and should not be used for operations with different radionuclides or processes.

Strange, D. L.; Bander, T. J.

1981-04-01T23:59:59.000Z

345

Depleted uranium disposition study -- Supplement, Revision 1  

SciTech Connect (OSTI)

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

Becker, G.W.

1993-11-01T23:59:59.000Z

346

In situ remediation of uranium contaminated groundwater  

SciTech Connect (OSTI)

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

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

1997-12-31T23:59:59.000Z

347

In situ remediation of uranium contaminated groundwater  

SciTech Connect (OSTI)

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

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

1997-02-01T23:59:59.000Z

348

Method of recovering uranium from aqueous solution  

SciTech Connect (OSTI)

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

Albright, R.L.

1980-01-22T23:59:59.000Z

349

Innovative design of uranium startup fast reactors  

E-Print Network [OSTI]

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

Fei, Tingzhou

2012-01-01T23:59:59.000Z

350

CRAD, Radioactive Waste Management- June 22, 2009  

Broader source: Energy.gov [DOE]

Radioactive Waste Management, Inspection Criteria, Approach, and Lines of Inquiry (HSS CRAD 64-33, Rev. 0)

351

Characterization of uranium in surface-waters collected at the Rocky Flats Facility  

SciTech Connect (OSTI)

The Rocky Flats Plant (RFP) is a Department of Energy (DOE) facility where plutonium and uranium components were manufactured for nuclear weapons. During plant operations radioactivity was inadvertently released into the environment. This study was initiated to characterize the uranium present in surface-waters at RFP. Three drainage basins and natural ephemeral streams transverse RFP. The Woman Creek drainage basin traverses and drains the southern portion of the site. The Rock Creek drainage basin drains the northwestern portion of the plant complex. The Walnut Creek drainage basin traverses the western, northern, and northeastern portions of the RFP site. Dams, detention ponds, diversion structures, and ditches have been constructed at RFP to control the release of plant discharges and surface (storm water) runoff. The ponds located downstream of the plant complex on North Walnut Creek are designated A-1 through A-4. Ponds on South Walnut Creek are designated B-1 through B-5. The ponds in the Woman Creek drainage basin are designated C-1 and C-2. Water samples were collected from each pond and the uranium was characterized by TIMS measurement techniques.

Efurd, D.W.; Rokop, D.J.; Aguilar, R.D.; Roensch, F.R.; Perrin, R.E.; Banar, J.C.

1994-06-01T23:59:59.000Z

352

[Uranium Mill Tailings Remedial Action Project Office Quality Assurance Program Plan]. Revision 4  

SciTech Connect (OSTI)

The Uranium Mill Tailings Remedial Action (UMTRA) Project was established to accomplish remedial actions at inactive uranium mill tailings sites in accordance with Public Law 95-604, the Uranium Mill Tailings Radiation Control Act of 1978 (UMTRCA). The UMTRA Project`s mission is to stabilize and control the residual radioactive materials at designated sites in a safe and environmentally sound manner so as to minimize or eliminate radiation health hazards to the public. The US Department of Energy (DOE) UMTRA Project Office (UMTRA PO) directs the overall project. Since these efforts may involve possible risks to public health and safety, a quality assurance (QA) program that conforms to the applicable criteria (set forth in the reference documents) has been established to control the quality of the work. This document, the Quality Assurance Program Plan (QAPP), brings into one document the essential criteria to be applied on a selective basis, depending upon the nature of the activity being conducted, and describes how those criteria shall be applied to the UMTRA Project. The UMTRA PO shall require each Project contractor to prepare and submit for approval a more detailed QAPP that is based on the applicable criteria of this QAPP and the referenced documents. All QAPPs on the UMTRA Project shall fit within the framework of this plan.

Not Available

1992-06-01T23:59:59.000Z

353

[Uranium Mill Tailings Remedial Action Project Office Quality Assurance Program Plan  

SciTech Connect (OSTI)

The Uranium Mill Tailings Remedial Action (UMTRA) Project was established to accomplish remedial actions at inactive uranium mill tailings sites in accordance with Public Law 95-604, the Uranium Mill Tailings Radiation Control Act of 1978 (UMTRCA). The UMTRA Project's mission is to stabilize and control the residual radioactive materials at designated sites in a safe and environmentally sound manner so as to minimize or eliminate radiation health hazards to the public. The US Department of Energy (DOE) UMTRA Project Office (UMTRA PO) directs the overall project. Since these efforts may involve possible risks to public health and safety, a quality assurance (QA) program that conforms to the applicable criteria (set forth in the reference documents) has been established to control the quality of the work. This document, the Quality Assurance Program Plan (QAPP), brings into one document the essential criteria to be applied on a selective basis, depending upon the nature of the activity being conducted, and describes how those criteria shall be applied to the UMTRA Project. The UMTRA PO shall require each Project contractor to prepare and submit for approval a more detailed QAPP that is based on the applicable criteria of this QAPP and the referenced documents. All QAPPs on the UMTRA Project shall fit within the framework of this plan.

Not Available

1992-06-01T23:59:59.000Z

354

Environmental assessment of remedial action at the Naturita Uranium Processing Site near Naturita, Colorado. Revision 4  

SciTech Connect (OSTI)

The Uranium Mill Tailings Radiation Control Act (UMTRCA) of 1978, Public Law (PL) 95-604, authorized the US Department of Energy (DOE) to perform remedial action at the Naturita, Colorado, uranium processing site to reduce the potential health effects from the radioactive materials at the site and at vicinity properties associated with the site. The US Environmental Protection Agency (EPA) promulgated standards for the UMTRCA that contain measures to control the contaminated materials and to protect groundwater quality. Remedial action at the Naturita site must be performed in accordance with these standards and with the concurrence of the US Nuclear Regulatory Commission (NRC) and the state of Colorado. The proposed remedial action for the Naturita processing site is relocation of the contaminated materials and debris to either the Dry Flats disposal site, 6 road miles (mi) [10 kilometers (km)] to the southeast, or a licensed non-DOE disposal facility capable of handling RRM. At either disposal site, the contaminated materials would be stabilized and covered with layers of earth and rock. The proposed Dry Flats disposal site is on land administered by the Bureau of Land Management (BLM) and used primarily for livestock grazing. The final disposal site would cover approximately 57 ac (23 ha), which would be permanently transferred from the BLM to the DOE and restricted from future uses. The remedial action would be conducted by the DOE`s Uranium Mill Tailings Remedial Action (UMTRA) Project. This report discusses environmental impacts associated with the proposed remedial action.

Not Available

1994-05-01T23:59:59.000Z

355

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

SciTech Connect (OSTI)

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

REGUERA, GEMMA [Michigan State University

2014-01-16T23:59:59.000Z

356

The ultimate disposition of depleted uranium  

SciTech Connect (OSTI)

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

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

1991-12-31T23:59:59.000Z

357

BIOREMEDIATION OF URANIUM CONTAMINATED SOILS AND WASTES.  

SciTech Connect (OSTI)

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

FRANCIS,A.J.

1998-09-17T23:59:59.000Z

358

Material property correlations for uranium mononitride  

E-Print Network [OSTI]

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

Hayes, Steven Lowe

2012-06-07T23:59:59.000Z

359

Spills of Radioactive Materials -Emergency Procedures  

E-Print Network [OSTI]

to radioactive waste container. For surface decontamination, use soap and water and cleansers appropriateSpills of Radioactive Materials - Emergency Procedures Procedure: 7.53 Created: 1/16/2014 Version for injured personnel. B. Applicability/scope This policy applies to all facilities where radioactive

Jia, Songtao

360

Laboratory Surveys when Working with Radioactive Materials  

E-Print Network [OSTI]

radioactive materials (RAM) are used or stored, including waste areas. Negative results should be clearlyLaboratory Surveys when Working with Radioactive Materials Procedure: 7.546 Created: 9/25/14 Version: 1.0 Revised: Environmental Health & Safety Page 1 of 6 A. Purpose Radioactive contamination and

Jia, Songtao

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


361

Environmental Radioactivity in Greenland in 1981  

E-Print Network [OSTI]

Ris-R-471 v Environmental Radioactivity in Greenland in 1981 A. Aarkrog, Henning Dahlgaard, Elis July 1962 #12;Ris-R-471 ENVIRONMENTAL RADIOACTIVITY IN GREENLAND IN 1981 A. Aarkrog, Henning Dahlgaard. Measurements of fallout radioactivity in Greenland in 1981 are reported. Strontium-90 (and Cesium-137 in most

362

Environmental Radioactivity in Greenland in 1978  

E-Print Network [OSTI]

ft I la 0 0 0 0 Risn-R-405 Environmental Radioactivity in Greenland in 1978 A. Aarkrog, Heinz ENVIRONMENTAL RADIOACTIVITY IN GREENLAND IN 1978 A. Aarkrog, Heinz Hansen and J. Lippert Abstract. Heasureaents of fallout radioactivity in Greenland in 1978 are reported. Strontium-90 (and Cesium-137 in most cases

363

Radioactivity in Food and the Environment, 1997  

E-Print Network [OSTI]

Radioactivity in Food and the Environment, 1997 RIFE - 3 1998 SCOTTISH ENVIRONMENT PROTECTION SCOTTISH ENVIRONMENT PROTECTION AGENCY Radioactivity in Food and the Environment, 1997 September 1998 #12 Environment Protection Agency in 1997. Measurements of radioactivity have been carried out in a range

364

Radioactive isotopes in Danish drinking water  

E-Print Network [OSTI]

Radioactive isotopes in Danish drinking water Sven P. Nielsen Risø National Laboratory Working OF INVESTIGATION 11 3 DESCRIPTION OF INVESTIGATION 12 4 RADIOACTIVITY IN DRINKING WATER 13 5 SAMPLING 15 6 27 #12;4 #12;5 Preface This project for investigation of radioactivity in drinking water shall

365

Electrochemical method of producing eutectic uranium alloy and apparatus  

DOE Patents [OSTI]

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

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

1995-01-01T23:59:59.000Z

366

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

SciTech Connect (OSTI)

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

NONE

1995-07-05T23:59:59.000Z

367

Radio-Ecological Conditions of Groundwater in the Area of Uranium Mining and Milling Facility - 13525  

SciTech Connect (OSTI)

Manmade chemical and radioactive contamination of groundwater is one of damaging effects of the uranium mining and milling facilities. Groundwater contamination is of special importance for the area of Priargun Production Mining and Chemical Association, JSC 'PPMCA', because groundwater is the only source of drinking water. The paper describes natural conditions of the site, provides information on changes of near-surface area since the beginning of the company, illustrates the main trends of contaminators migration and assesses manmade impact on the quality and mode of near-surface and ground waters. The paper also provides the results of chemical and radioactive measurements in groundwater at various distances from the sources of manmade contamination to the drinking water supply areas. We show that development of deposits, mine water discharge, leakages from tailing dams and cinder storage facility changed general hydro-chemical balance of the area, contributed to new (overlaid) aureoles and flows of scattering paragenetic uranium elements, which are much smaller in comparison with natural ones. However, increasing flow of groundwater stream at the mouth of Sukhoi Urulyungui due to technological water infiltration, mixing of natural water with filtration streams from industrial reservoirs and sites, containing elevated (relative to natural background) levels of sulfate-, hydro-carbonate and carbonate- ions, led to the development and moving of the uranium contamination aureole from the undeveloped field 'Polevoye' to the water inlet area. The aureole front crossed the southern border of water inlet of drinking purpose. The qualitative composition of groundwater, especially in the southern part of water inlet, steadily changes for the worse. The current Russian intervention levels of gross alpha activity and of some natural radionuclides including {sup 222}Rn are in excess in drinking water; regulations for fluorine and manganese concentrations are also in excess. Possible ways to improve the situation are considered. (authors)

Titov, A.V.; Semenova, M.P.; Seregin, V.A.; Isaev, D.V.; Metlyaev, E.G. [FSBU SRC A.I.Burnasyan Federal Medical Biophysical Center of FMBA of Russia, Zhivopisnaya Street, 46, Moscow (Russian Federation)] [FSBU SRC A.I.Burnasyan Federal Medical Biophysical Center of FMBA of Russia, Zhivopisnaya Street, 46, Moscow (Russian Federation); Glagolev, A.V.; Klimova, T.I.; Sevtinova, E.B. [FSESP 'Hydrospecgeologiya' (Russian Federation)] [FSESP 'Hydrospecgeologiya' (Russian Federation); Zolotukhina, S.B.; Zhuravleva, L.A. [FSHE 'Centre of Hygiene and Epidemiology no. 107' under FMBA of Russia (Russian Federation)] [FSHE 'Centre of Hygiene and Epidemiology no. 107' under FMBA of Russia (Russian Federation)

2013-07-01T23:59:59.000Z

368

Determination of aerosol size distributions at uranium mill tailings remedial action project sites  

SciTech Connect (OSTI)

The U.S. Department of Energy (DOE) has an ongoing program, the Uranium Mill Tailings Remedial Action (UMTRA) Project, to stabilize piles of uranium mill tailings in order to reduce the potential radiological hazards to the public. Protection of workers and the general public against airborne radioactivity during remedial action is a top priority at the UMTRA Project. The primary occupational radionuclides of concern are {sup 230}Th, {sup 226}Ra, {sup 210}Pb, {sup 210}Po, and the short-lived decay products of {sup 222}Rn with {sup 230}Th causing the majority of the committed effective dose equivalent (CEDE) from inhaling uranium mill tailings. Prior to this study, a default particle size of 1.0 {mu}m activity median aerodynamic diameter (AMAD) was assumed for airborne radioactive tailings dust. Because of recent changes in DOE requirements, all DOE operations are now required to use the CEDE methodology, instead of the annual effective dose equivalent (AEDE) methodology, to evaluate internal radiation exposures. Under the transition from AEDE to CEDE, with a 1.0 {mu}m AMAD particle size, lower bioassay action levels would be required for the UMTRA Project. This translates into an expanded internal dosimetry program where significantly more bioassay monitoring would be required at the UMTRA Project sites. However, for situations where the particle size distribution is known to differ significantly from 1.0 {mu}m AMAD, the DOE allows for corrections to be made to both the estimated dose to workers and the derived air concentration (DAC) values. For particle sizes larger than 1.0 {mu}m AMAD, the calculated CEDE from inhaling tailings would be relatively lower.

Newton, G.J.; Reif, R.H. [CWM Federal Environmental Services, Inc., Albuquerque, NM (United States); Hoover, M.D.

1994-11-01T23:59:59.000Z

369

Determination of the Relative Amount of Fluorine in Uranium Oxyfluoride Particles using Secondary Ion Mass Spectrometry and Optical Spectroscopy  

SciTech Connect (OSTI)

Both nuclear forensics and environmental sampling depend upon laboratory analysis of nuclear material that has often been exposed to the environment after it has been produced. It is therefore important to understand how those environmental conditions might have changed the chemical composition of the material over time, particularly for chemically sensitive compounds. In the specific case of uranium enrichment facilities, uranium-bearing particles stem from small releases of uranium hexafluoride, a highly reactive gas that hydrolyzes upon contact with moisture from the air to form uranium oxyfluoride (UO{sub 2}F{sub 2}) particles. The uranium isotopic composition of those particles is used by the International Atomic Energy Agency (IAEA) to verify whether a facility is compliant with its declarations. The present study, however, aims to demonstrate how knowledge of time-dependent changes in chemical composition, particle morphology and molecular structure can contribute to an even more reliable interpretation of the analytical results. We prepared a set of uranium oxyfluoride particles at the Institute for Reference Materials and Measurements (IRMM, European Commission, Belgium) and followed changes in their composition, morphology and structure with time to see if we could use these properties to place boundaries on the particle exposure time in the environment. Because the rate of change is affected by exposure to UV-light, humidity levels and elevated temperatures, the samples were subjected to varying conditions of those three parameters. The NanoSIMS at LLNL was found to be the optimal tool to measure the relative amount of fluorine in individual uranium oxyfluoride particles. At PNNL, cryogenic laser-induced time-resolved U(VI) fluorescence microspectroscopy (CLIFS) was used to monitor changes in the molecular structure.

Kips, R; Kristo, M J; Hutcheon, I D; Amonette, J; Wang, Z; Johnson, T; Gerlach, D; Olsen, K B

2009-05-29T23:59:59.000Z

370

A Characteristics-Based Approach to Radioactive Waste Classification in Advanced Nuclear Fuel Cycles  

E-Print Network [OSTI]

05-?20 Regarding Depleted Uranium. Rulemaking Issue (Department of Energy depleted uranium Environmental waste (MLLW) and depleted uranium (DU) from

Djokic, Denia

2013-01-01T23:59:59.000Z

371

Baseline risk assessment of groundwater contamination at the Uranium Mill Tailings Site near Gunnison, Colorado. Revision 1  

SciTech Connect (OSTI)

This report evaluates potential impacts to public health or the environment resulting from groundwater contamination at the former uranium mill processing site. The tailings and other contaminated material at this site are being placed in an off-site disposal cell by the US Department of Energy`s (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project. Currently, the UMTRA Project is evaluating groundwater contamination. This is the second risk assessment of groundwater contamination at this site. The first risk assessment was performed primarily to evaluate existing domestic wells to determine the potential for immediate human health and environmental impacts. This risk assessment evaluates the most contaminated groundwater that flows beneath the processing site towards the Gunnison River. The monitor wells that have consistently shown the highest concentration of most contaminants are used in this risk assessment. This risk assessment will be used in conjunction with additional activities and documents to assist in determining what remedial action is needed for contaminated groundwater at the site after the tailings are relocated. This risk assessment follows an approach outlined by the US Environmental Protection Agency (EPA). The first step is to evaluate groundwater data collected from monitor wells at the site. Evaluation of these data showed that the main contaminants in the groundwater are cadmium, cobalt, iron, manganese, sulfate, uranium, and some of the products of radioactive decay of uranium.

Not Available

1994-04-01T23:59:59.000Z

372

Radioactive waste treatment technologies and environment  

SciTech Connect (OSTI)

The radioactive waste treatment and conditioning are the most important steps in radioactive waste management. At the Slovak Electric, plc, a range of technologies are used for the processing of radioactive waste into a form suitable for disposal in near surface repository. These technologies operated by JAVYS, PLc. Nuclear and Decommissioning Company, PLc. Jaslovske Bohunice are described. Main accent is given to the Bohunice Radwaste Treatment and Conditioning Centre, Bituminization plant, Vitrification plant, and Near surface repository of radioactive waste in Mochovce and their operation. Conclusions to safe and effective management of radioactive waste in the Slovak Republic are presented. (authors)

HORVATH, Jan; KRASNY, Dusan [JAVYS, PLc. - Nuclear and Decommisioning Company, PLc. (Slovakia)

2007-07-01T23:59:59.000Z

373

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

SciTech Connect (OSTI)

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

Knight, J.R.

1984-11-01T23:59:59.000Z

374

Microoptical compound lens  

DOE Patents [OSTI]

An apposition microoptical compound lens comprises a plurality of lenslets arrayed around a segment of a hollow, three-dimensional optical shell. The lenslets collect light from an object and focus the light rays onto the concentric, curved front surface of a coherent fiber bundle. The fiber bundle transports the light rays to a planar detector, forming a plurality of sub-images that can be reconstructed as a full image. The microoptical compound lens can have a small size (millimeters), wide field of view (up to 180.degree.), and adequate resolution for object recognition and tracking.

Sweatt, William C. (Albuquerque, NM); Gill, David D. (Albuquerque, NM)

2007-10-23T23:59:59.000Z

375

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

SciTech Connect (OSTI)

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

none,

1981-10-01T23:59:59.000Z

376

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

SciTech Connect (OSTI)

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

none,

1981-09-01T23:59:59.000Z

377

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

SciTech Connect (OSTI)

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

none,

1981-09-01T23:59:59.000Z

378

Environmental assessment of remedial action at the Slick Rock uranium mill tailings sites Slick Rock, Colorado. Draft  

SciTech Connect (OSTI)

The Uranium Mill Tailings Radiation Control Act of 1978 (UMTRCA) authorized the US Department of Energy (DOE) to clean up two uranium mill tailings processing sites near Slick Rock, Colorado, in San Miguel County. The purpose of the cleanup is to reduce the potential health effects associated with the radioactive materials remaining on the sites and on vicinity properties (VP) associated with the sites. The US Environmental Protection Agency (EPA) promulgated standards for the UMTRCA that contained measures to control the contaminated materials and to protect the groundwater from further degradation. Remedial actions at the Slick Rock sites must be performed in accordance with these standards and with the concurrence of the US Nuclear Regulatory Commission (NRC).

NONE

1993-06-01T23:59:59.000Z

379

Aminopropyl thiophene compounds  

DOE Patents [OSTI]

Radiopharmaceuticals useful in brain imaging comprising radiohalogenated thienylethylamine derivatives. The compounds are 5-halo-thiophene-2-isopropyl amines able to cross the blood-brain barrier and be retained for a sufficient length of time to allow the evaluation of regional blood flow by radioimaging of the brain.

Goodman, Mark M. (Knoxville, TN); Knapp, Jr., Furn F. (Oak Ridge, TN)

1990-01-01T23:59:59.000Z

380

Engineering study of 50 miscellaneous inactive underground radioactive waste tanks located at the Hanford Site, Washington  

SciTech Connect (OSTI)

This engineering study addresses 50 inactive underground radioactive waste tanks. The tanks were formerly used for the following functions associated with plutonium and uranium separations and waste management activities in the 200 East and 200 West Areas of the Hanford Site: settling solids prior to disposal of supernatant in cribs and a reverse well; neutralizing acidic process wastes prior to crib disposal; receipt and processing of single-shell tank (SST) waste for uranium recovery operations; catch tanks to collect water that intruded into diversion boxes and transfer pipeline encasements and any leakage that occurred during waste transfer operations; and waste handling and process experimentation. Most of these tanks have not been in use for many years. Several projects have, been planned and implemented since the 1970`s and through 1985 to remove waste and interim isolate or interim stabilize many of the tanks. Some tanks have been filled with grout within the past several years. Responsibility for final closure and/or remediation of these tanks is currently assigned to several programs including Tank Waste Remediation Systems (TWRS), Environmental Restoration and Remedial Action (ERRA), and Decommissioning and Resource Conservation and Recovery Act (RCRA) Closure (D&RCP). Some are under facility landlord responsibility for maintenance and surveillance (i.e. Plutonium Uranium Extraction [PUREX]). However, most of the tanks are not currently included in any active monitoring or surveillance program.

Freeman-Pollard, J.R.

1994-03-02T23:59:59.000Z

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


381

EA-1290: Disposition of Russian Federation Titled Natural Uranium  

Broader source: Energy.gov [DOE]

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

382

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

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

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

383

Assessments of long-term uranium supply availability  

E-Print Network [OSTI]

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

Zaterman, Daniel R

2009-01-01T23:59:59.000Z

384

Prospects for the recovery of uranium from seawater  

E-Print Network [OSTI]

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

Best, F. R.

1980-01-01T23:59:59.000Z

385

Single-Pass Flow-Through Test Elucidation of Weathering Behavior and Evaluation of Contaminant Release Models for Hanford Tank Residual Radioactive Waste  

SciTech Connect (OSTI)

Contaminant release models are required to evaluate and predict long-term environmental impacts of even residual amounts of high-level radioactive waste after cleanup and closure of radioactively contaminated sites such as the DOEs Hanford Site. More realistic and representative models have been developed for release of uranium, technetium, and chromium from Hanford Site tanks C-202, C-203, and C-103 residual wastes using data collected with a single-pass flow-through test (SPFT) method. These revised models indicate that contaminant release concentrations from these residual wastes will be considerably lower than previous estimates based on batch experiments. For uranium, a thermodynamic solubility model provides an effective description of uranium release, which can account for differences in pore fluid chemistry contacting the waste that could occur through time and as a result of different closure scenarios. Under certain circumstances in the SPFT experiments various calcium rich precipitates (calcium phosphates and calcite) form on the surfaces of the waste particles, inhibiting dissolution of the underlying uranium phases in the waste. This behavior was not observed in previous batch experiments. For both technetium and chromium, empirical release models were developed. In the case of technetium, release from all three wastes was modeled using an equilibrium Kd model. For chromium release, a constant concentration model was applied for all three wastes.

Cantrell, Kirk J.; Carroll, Kenneth C.; Buck, Edgar C.; Neiner, Doinita; Geiszler, Keith N.

2013-01-01T23:59:59.000Z

386

The use of non-destructive passive neutron measurement methods in dismantling and radioactive waste characterization  

SciTech Connect (OSTI)

The cleaning up and dismantling of nuclear facilities lead to a great volume of technological radioactive wastes which need to be characterized in order to be sent to the adequate final disposal or interim storage. The control and characterization can be performed with non-destructive nuclear measurements such as gamma-ray spectrometry. Passive neutron counting is an alternative when the alpha-gamma emitters cannot be detected due to the presence of a high gamma emission resulting from fission or activation products, or when the waste matrix is too absorbing for the gamma rays of interest (too dense and/or made of high atomic number elements). It can also be a complement to gamma-ray spectrometry when two measurement results must be confronted to improve the confidence in the activity assessment. Passive neutron assays involve the detection of spontaneous fission neutrons emitted by even nuclides ({sup 238}Pu, {sup 240}Pu, {sup 242}Pu, {sup 242}Cm, {sup 244}Cm...) and neutrons resulting from ({alpha}, n) reactions with light nuclides (O, F, Be...). The latter is conditioned by the presence of high {alpha}-activity radionuclides ({sup 234}U, {sup 238}Pu, {sup 240}Pu, {sup 241}Am...) and low-Z elements, which depends on the chemical form (metallic, oxide or fluorine) of the plutonium or uranium contaminant. This paper presents the recent application of passive neutron methods to the cleaning up of a nuclear facility located at CEA Cadarache (France), which concerns the Pu mass assessment of 2714 historic, 100 litre radioactive waste drums produced between 1980 and 1997. Another application is the dismantling and decommissioning of an uranium enrichment facility for military purposes, which involves the {sup 235}U and total uranium quantifications in about a thousand, large compressors employed in the gaseous diffusion enrichment process. (authors)

Jallu, F.; Allinei, P. G. [CEA, DEN, Cadarache, Nuclear Measurement Laboratory, F-13108 Saint-Paul-lez-Durance (France); Bernard, P.; Loridon, J. [CEA, DEN, Cadarache, Nuclear Measurement Laboratory, F-13108 Saint-Paul-lez-Durance (France); Soyer, P.; Pouyat, D. [CEA, DEN, Marcoule, DPAD, F-30207 Bagnols-sur-Ceze Cedex (France); Torreblanca, L. [CEA, DEN, Cadarache, LMDE, F-13108 Saint-Paul-lez-Durance (France); Reneleau, A. [AREVA NC, Pierrelatte, DDAC/ESD, BP16, F-26701 Pierrelatte Cedex (France)

2011-07-01T23:59:59.000Z

387

Radioactive Waste Management and Nuclear Facility Decommissioning Progress in Iraq - 13216  

SciTech Connect (OSTI)

Management of Iraq's radioactive wastes and decommissioning of Iraq's former nuclear facilities are the responsibility of Iraq's Ministry of Science and Technology (MoST). The majority of Iraq's former nuclear facilities are in the Al-Tuwaitha Nuclear Research Center located a few kilometers from the edge of Baghdad. These facilities include bombed and partially destroyed research reactors, a fuel fabrication facility and radioisotope production facilities. Within these facilities are large numbers of silos, approximately 30 process or waste storage tanks and thousands of drums of uncharacterised radioactive waste. There are also former nuclear facilities/sites that are outside of Al-Tuwaitha and these include the former uranium processing and waste storage facility at Jesira, the dump site near Adaya, the former centrifuge facility at Rashdiya and the former enrichment plant at Tarmiya. In 2005, Iraq lacked the infrastructure needed to decommission its nuclear facilities and manage its radioactive wastes. The lack of infrastructure included: (1) the lack of an organization responsible for decommissioning and radioactive waste management, (2) the lack of a storage facility for radioactive wastes, (3) the lack of professionals with experience in decommissioning and modern waste management practices, (4) the lack of laws and regulations governing decommissioning or radioactive waste management, (5) ongoing security concerns, and (6) limited availability of electricity and internet. Since its creation eight years ago, the MoST has worked with the international community and developed an organizational structure, trained staff, and made great progress in managing radioactive wastes and decommissioning Iraq's former nuclear facilities. This progress has been made, despite the very difficult implementing conditions in Iraq. Within MoST, the Radioactive Waste Treatment and Management Directorate (RWTMD) is responsible for waste management and the Iraqi Decommissioning Directorate (IDD) is responsible for decommissioning activities. The IDD and the RWTMD work together on decommissioning projects. The IDD has developed plans and has completed decommissioning of the GeoPilot Facility in Baghdad and the Active Metallurgical Testing Laboratory (LAMA) in Al-Tuwaitha. Given this experience, the IDD has initiated work on more dangerous facilities. Plans are being developed to characterize, decontaminate and decommission the Tamuz II Research Reactor. The Tammuz Reactor was destroyed by an Israeli air-strike in 1981 and the Tammuz II Reactor was destroyed during the First Gulf War in 1991. In addition to being responsible for managing the decommissioning wastes, the RWTMD is responsible for more than 950 disused sealed radioactive sources, contaminated debris from the first Gulf War and (approximately 900 tons) of naturally-occurring radioactive materials wastes from oil production in Iraq. The RWTMD has trained staff, rehabilitated the Building 39 Radioactive Waste Storage building, rehabilitated portions of the French-built Radioactive Waste Treatment Station, organized and secured thousands of drums of radioactive waste organized and secured the stores of disused sealed radioactive sources. Currently, the IDD and the RWTMD are finalizing plans for the decommissioning of the Tammuz II Research Reactor. (authors)

Al-Musawi, Fouad; Shamsaldin, Emad S.; Jasim, Hadi [Ministry of Science and Technology (MoST), Al-Jadraya, P.O. Box 0765, Baghdad (Iraq)] [Ministry of Science and Technology (MoST), Al-Jadraya, P.O. Box 0765, Baghdad (Iraq); Cochran, John R. [Sandia National Laboratories1, New Mexico, Albuquerque New Mexico 87185 (United States)] [Sandia National Laboratories1, New Mexico, Albuquerque New Mexico 87185 (United States)

2013-07-01T23:59:59.000Z

388

A thick homogeneous vegetated cover design proves cost - and schedule-effective for the reclamation of uranium mills sites near Spokane, Washington  

SciTech Connect (OSTI)

The Washington State Department of Health (WDOH) has licensed two medium sized uranium mills with tailings impoundments covering 28 and 40 hectares (70 and 100 acres), respectively, The uranium mill licensees have submitted closure and reclamation plans to the state, and site-specific conditions have determined the closure design features, Conventional uranium mill cover designs usually incorporate an overall cap of one to three meters, which includes a low-permeability clay barrier layer. A technical evaluation of several uranium mill facilities that used this design was published in the fall of 1994 and reported that unexpected vegetation root damage had occurred in the low-permeability clay (or bentonite amended) barrier layers. The technical report suggested that the low-permeability design feature at some sites could be compromised within a very short time and the regulatory goal of 1,000 years performance might not be achieved. In October 1994, WDOH sponsored a technical forum meeting to consider design alternatives to address these reliability concerns. Representatives from the federal government, nuclear industry, licensees, engineering firms, and state regulatory agencies attended the workshop. Risk factors considered in the evaluation of the uranium mill reclamation plans include: (1) radon gas emanation through the cover (the air pathway), and (2) migration of hazardous and/or radioactive constituents (the groundwater pathway). Additional design considerations include site structural stability, longevity of 1,000 years, and no active (ongoing) maintenance. 9 refs.

Blacklaw, J.; Robertson, G.; Stoffel, D.; Ahmad, J.; Fordham, E. [Washington State Dept. of Health, Olympia, WA (United States)] [and others

1997-08-01T23:59:59.000Z

389

Monitoring Uranium Transformations Determined by the Evolution of Biogeochemical Processes  

SciTech Connect (OSTI)

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

Marsh, Terence L.

2013-07-30T23:59:59.000Z

390

Depleted Uranium in Kosovo Post-Conflict Environmental Assessment  

E-Print Network [OSTI]

2.1 UNEPs role in post-conflict environmental assessment................................................9 2.2 Depleted uranium............................................................10

Unep Scientific; Mission Kosovo

391

Integrated Data Base for 1992: US spent fuel and radioactive waste inventories, projections, and characteristics. Revision 8  

SciTech Connect (OSTI)

The Integrated Data Base (IDB) Program has compiled current data on inventories and characteristics of commercial spent fuel and both commercial and US government-owned radioactive wastes through December 31, 1991. These data are based on the most reliable information available from government sources, the open literature, technical reports, and direct contacts. The information forecasted is consistent with the latest US Department of Energy/Energy Information Administration (DOE/EIA) projections of US commercial nuclear power growth and the expected DOE-related and private industrial and institutional (I/I) activities. The radioactive materials considered, on a chapter-by-chapter basis, are spent nuclear fuel, high-level waste, transuranic waste, low-level waste, commercial uranium mill tailings, environmental restoration wastes, commercial reactor and fuel cycle facility decommissioning wastes, and mixed (hazardous and radioactive) low-level waste. For most of these categories, current and projected inventories are given through the year 2030, and the radioactivity and thermal power are calculated based on reported or estimated isotopic compositions. In addition, characteristics and current inventories are reported for miscellaneous radioactive materials that may require geologic disposal.

Not Available

1992-10-01T23:59:59.000Z

392

Integrated Data Base report--1993: U.S. spent nuclear fuel and radioactive waste inventories, projections, and characteristics. Revision 10  

SciTech Connect (OSTI)

The Integrated Data Base Program has compiled historic data on inventories and characteristics of both commercial and DOE spent nuclear fuel; also, commercial and US government-owned radioactive wastes through December 31, 1993. These data are based on the most reliable information available from government sources, the open literature, technical reports, and direct contacts. The information forecasted is consistent with the latest US Department of Energy/Energy Information Administration projections of US commercial nuclear power growth and the expected DOE-related and private industrial and institutional activities. The radioactive materials considered, on a chapter-by-chapter basis, are spent nuclear fuel, high-level waste, transuranic waste, low-level waste, commercial uranium mill tailings, DOE Environmental Restoration Program wastes, commercial reactor and fuel-cycle facility decommissioning wastes, and mixed (hazardous and radioactive) low-level waste. For most of these categories, current and projected inventories are given the calendar-year 2030, and the radioactivity and thermal power are calculated based on reported or estimated isotopic compositions. In addition, characteristics and current inventories are reported for miscellaneous radioactive materials that may require geologic disposal. 256 refs., 38 figs., 141 tabs.

Not Available

1994-12-01T23:59:59.000Z

393

Integrated data base for 1993: US spent fuel and radioactive waste inventories, projections, and characteristics. Revision 9  

SciTech Connect (OSTI)

The Integrated Data Base (IDB) Program has compiled historic data on inventories and characteristics of both commercial and DOE spent fuel; also, commercial and U.S. government-owned radioactive wastes through December 31, 1992. These data are based on the most reliable information available from government sources, the open literature, technical reports, and direct contacts. The information forecasted is consistent with the latest U.S. Department of Energy/Energy Information Administration (DOE/EIA) projections of U.S. commercial nuclear power growth and the expected DOE-related and private industrial and institutional (I/I) activities. The radioactive materials considered, on a chapter-by-chapter basis, are spent nuclear fuel, high-level waste (HLW), transuranic (TRU), waste, low-level waste (LLW), commercial uranium mill tailings, environmental restoration wastes, commercial reactor and fuel-cycle facility decommissioning wastes, and mixed (hazardous and radioactive) LLW. For most of these categories, current and projected inventories are given through the calendar-year (CY) 2030, and the radioactivity and thermal power are calculated based on reported or estimated isotopic compositions. In addition, characteristics and current inventories are reported for miscellaneous radioactive materials that may require geologic disposal.

Klein, J.A.; Storch, S.N.; Ashline, R.C. [and others

1994-03-01T23:59:59.000Z

394

Remedial actions at the former Climax Uranium Company, Uranium Mill site, Grand Junction, Mesa County, Colorado. Volume 1, Text: Final environmental impact statement  

SciTech Connect (OSTI)

This statement evaluates and compares the environmental impacts associated with the remedial actions of the residual radioactive materials remaining at the inactive uranium processing site and associated vicinity properties at Grand Junction, Mesa County, Colorado. This statement is also intended to aid the BLM in amending their management framework plans and final resource management plan, as well as assisting in compliance with the withdrawal application as appropriate. The site is a 114-acre tract of private and state owned land which contains approximately 3.1 million cubic yards of tailings and associated contaminated soils. The vicinity properties are homes, businesses, public buildings, and vacant lots which may have been contaminated during construction by the use of tailings as building material. An estimated 3465 vicinity properties would be cleaned up during remedial action of the tailings pile. The tailings were produced by the former Climax Uranium Company which processed uranium ore, which it sold to the US Atomic Energy Commission from 1951 to 1966 and to private sources from 1966 to 1970. This statement evaluates six alternatives for stabilization and disposal of the tailings and other contaminated materials: (1) No action. (2) Stabilization at the Grand Junction site. (3) Disposal at the Cheney Reservoir site with truck transport. (4) Disposal at the Cheney Reservoir site with train and truck transport. (5) Disposal at the Two Road site with truck transport. (6) Disposal at the Two Road site with train and truck transport. All of the alternatives except no action include remedial action at an estimated 3465 vicinity properties. Alternative 3 is DOE`s preferred alternative.

None

1986-12-01T23:59:59.000Z

395

Microbial Janitors: Enabling natural microbes to clean up uranium contamination  

E-Print Network [OSTI]

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

396

Plutonium recovery from spent reactor fuel by uranium displacement  

DOE Patents [OSTI]

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

Ackerman, John P. (Downers Grove, IL)

1992-01-01T23:59:59.000Z

397

Standard Review Plan for In Situ Leach Uranium  

E-Print Network [OSTI]

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

398

Bioremediation of Uranium Plumes with Nano-scale  

E-Print Network [OSTI]

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

Fay, Noah

399

Plutonium recovery from spent reactor fuel by uranium displacement  

DOE Patents [OSTI]

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

Ackerman, J.P.

1992-03-17T23:59:59.000Z

400

Composition of the U.S. DOE Depleted Uranium Inventory  

E-Print Network [OSTI]

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

Concentration Of Less

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


401

Estimating terrestrial uranium and thorium by antineutrino flux measurements  

E-Print Network [OSTI]

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

Mcdonough, William F.

402

A Geostatistical Study of the Uranium Deposit at Kvanefjeld,  

E-Print Network [OSTI]

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

403

Depleted uranium plasma reduction system study  

SciTech Connect (OSTI)

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

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

1994-12-01T23:59:59.000Z

404

Depleted uranium hexafluoride: Waste or resource?  

SciTech Connect (OSTI)

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

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

1995-07-01T23:59:59.000Z

405

Method for fluorination of uranium oxide  

DOE Patents [OSTI]

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

Petit, George S. (Oak Ridge, TN)

1987-01-01T23:59:59.000Z

406

Radioactive Waste Management BasisSept 2001  

SciTech Connect (OSTI)

This Radioactive Waste Management Basis (RWMB) documents radioactive waste management practices adopted at Lawrence Livermore National Laboratory (LLNL) pursuant to Department of Energy (DOE) Order 435.1, Radioactive Waste Management. The purpose of this RWMB is to describe the systematic approach for planning, executing, and evaluating the management of radioactive waste at LLNL. The implementation of this document will ensure that waste management activities at LLNL are conducted in compliance with the requirements of DOE Order 435.1, Radioactive Waste Management, and the Implementation Guide for DOE manual 435.1-1, Radioactive Waste Management Manual. Technical justification is provided where methods for meeeting the requirements of DOE Order 435.1 deviate from the DOE Manual 435.1-1 and Implementation Guide.

Goodwin, S S

2011-08-31T23:59:59.000Z

407

Evaporation of Enriched Uranium Solutions Containing Organophosphates  

SciTech Connect (OSTI)

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

Pierce, R.A.

1999-03-18T23:59:59.000Z

408

Decarburization of uranium via electron beam processing  

SciTech Connect (OSTI)

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

McKoon, R H

1998-10-23T23:59:59.000Z

409

Progress toward uranium scrap recycling via EBCHR  

SciTech Connect (OSTI)

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

McKoon, R.H.

1994-11-01T23:59:59.000Z

410

Geochemical information for sites contaminated with low-level radioactive wastes. III. Weldon Spring Storage Site  

SciTech Connect (OSTI)

The Weldon Spring Storage Site (WSSS), which includes both the chemical site and the quarry, became radioactively contaminated as the result of wastes that were being stored from operations to recover uranium from pitchblende ores in the 1940s and 1950s. The US Department of Energy (DOE) is considering various remedial action options for the WSSS. This report describes the results of geochemical investigations carried out at Oak Ridge National Laboratory (ORNL) to support these activities and to help quantify various remedial action options. Soil and groundwater samples were characterized, and uranium and radium sorption ratios were measured in site soil/groundwater systems by batch contact methodology. Soil samples from various locations around the raffinate pits were found to contain major amounts of silica, along with illite as the primary clay constituent. Particle sizes of the five soil samples were variable (50% distribution point ranging from 12 to 81 ..mu..m); the surface areas varied from 13 to 62 m/sup 2//g. Elemental analysis of the samples showed them to be typical of sandy clay and silty clay soils. Groundwater samples included solution from Pit 3 and well water from Well D. Anion analyses showed significant concentrations of sulfate and nitrate (>350 and >7000 mg/L, respectively) in the solution from Pit 3. These anions were also present in the well water, but in lower concentrations. Uranium sorption ratios for four of the soil samples contacted with the solution from Pit 3 were moderate to high (approx. 300 to approx. 1000 mL/g). The fifth sample had a ratio of only 12 mL/g. Radium sorption ratios for the five samples were moderate to high (approx. 600 to approx. 1000 mL/g). These values indicate that soil at the WSSS may show favorable retardation of uranium and radium in the groundwater. 13 references, 13 figures, 10 tables.

Seeley, F.G.; Kelmers, A.D.

1985-02-01T23:59:59.000Z

411

Annual Transportation Report for Radioactive Waste Shipments...  

National Nuclear Security Administration (NNSA)

ANNUAL TRANSPORTATION REPORT FY 2008 Radioactive Waste Shipments to and from the Nevada Test Site (NTS) February 2009 United States Department of Energy National Nuclear Security...

412

Office of Civilian Radioactive Waste Management Transportation...  

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

Jay Jones Office of Civilian Radioactive Waste Management April 22, 2004 Albuquerque, New Mexico 2 Session Overview * Meeting objectives and expectations * Topic Group...

413

Radiation Machines and Radioactive Materials (Iowa)  

Broader source: Energy.gov [DOE]

These chapters describe general provisions and regulatory requirements; registration, licensure, and transportation of radioactive materials; and exposure standards for radiation protection.

414

Radiation Sources and Radioactive Materials (Connecticut)  

Broader source: Energy.gov [DOE]

These regulations apply to persons who receive, transfer, possess, manufacture, use, store, handle, transport or dispose of radioactive materials and/or sources of ionizing radiation. Some...

415

One million curies of radioactive material recovered  

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

Removal Program and OSRP mission includes removal and disposal of excess, unwanted, abandoned, or orphan radioactive sealed sources that pose a potential risk to national...

416

Radioactive Material Declaration Form Exhibit to the Radioactive Waste Manual (RWM)  

E-Print Network [OSTI]

Radioactive Material Declaration Form Exhibit to the Radioactive Waste Manual (RWM) 12/5/2013 (form Declaration Form Exhibit to the Radioactive Waste Manual (RWM) 12/5/2013 (form date) SLAC-I-760-2A08Z-001 (RWM date) SLAC-I-760-2A08Z-001 (RWM number) Page 1 of 2 RADIOACTIVE MATERIAL DECLARATION FORM For RP use

Wechsler, Risa H.

417

Cosmic radioactivity and INTEGRAL results  

SciTech Connect (OSTI)

Gamma-ray lines from radioactive decay of unstable isotopes co-produced by nucleosynthesis in massive stars and supernova have been measured since more than thirty years. Over the past ten years, INTEGRAL complemented the first sky survey made by COMPTEL. The {sup 26}A1 isotope with 1 My decay time had been first direct proof of currently-ongoing nucleosynthesis in our Galaxy. This has now become a tool to study the ?My history of specific source regions, such as massive-star groups and associations in nearby regions which can be discriminated from the galactic-plane background, and the inner Galaxy, where Doppler shifted lines add to the astronomical information about bar and spiral structure. Recent findings suggest that superbubbles show a remarkable asymmetry, on average, in the spiral arms of our galaxy. {sup 60}Fe is co-produced by the sources of {sup 26}A1, and the isotopic ratio from their nucleosynthesis encodes stellar-structure information. Annihilation gamma-rays from positrons in interstellar space show a puzzling bright and extended source region central to our Galaxy, but also may be partly related to nucleosynthesis. {sup 56}Ni and {sup 44}Ti isotope gamma-rays have been used to constrain supernova explosion mechanisms. Here we report latest results using the accumulated multi-year database of INTEGRAL observations, and discuss their astrophysical interpretations, connecting to other traces of cosmic radioactivity and to other cosmic messengers.

Diehl, Roland [Max Planck Institut fr Extraterrestrische Physik, D-85748 Garching, Germany and Excellence Cluster Origin and Evolution of the Universe', D-85748 Garching (Germany)

2014-05-02T23:59:59.000Z

418

Radioactive material package seal tests  

SciTech Connect (OSTI)

General design or test performance requirements for radioactive materials (RAM) packages are specified in Title 10 of the US Code of Federal Regulations Part 71 (US Nuclear Regulatory Commission, 1983). The requirements for Type B packages provide a broad range of environments under which the system must contain the RAM without posing a threat to health or property. Seals that provide the containment system interface between the packaging body and the closure must function in both high- and low-temperature environments under dynamic and static conditions. A seal technology program, jointly funded by the US Department of Energy Office of Environmental Restoration and Waste Management (EM) and the Office of Civilian Radioactive Waste Management (OCRWM), was initiated at Sandia National Laboratories. Experiments were performed in this program to characterize the behavior of several static seal materials at low temperatures. Helium leak tests on face seals were used to compare the materials. Materials tested include butyl, neoprene, ethylene propylene, fluorosilicone, silicone, Eypel, Kalrez, Teflon, fluorocarbon, and Teflon/silicone composites. Because most elastomer O-ring applications are for hydraulic systems, manufacturer low-temperature ratings are based on methods that simulate this use. The seal materials tested in this program with a fixture similar to a RAM cask closure, with the exception of silicone S613-60, are not leak tight (1.0 {times} 10{sup {minus}7} std cm{sup 3}/s) at manufacturer low-temperature ratings. 8 refs., 3 figs., 1 tab.

Madsen, M.M.; Humphreys, D.L.; Edwards, K.R.

1990-01-01T23:59:59.000Z

419

Selected radionuclides important to low-level radioactive waste management  

SciTech Connect (OSTI)

The purpose of this document is to provide information to state representatives and developers of low level radioactive waste (LLW) management facilities about the radiological, chemical, and physical characteristics of selected radionuclides and their behavior in the environment. Extensive surveys of available literature provided information for this report. Certain radionuclides may contribute significantly to the dose estimated during a radiological performance assessment analysis of an LLW disposal facility. Among these are the radionuclides listed in Title 10 of the Code of Federal Regulations Part 61.55, Tables 1 and 2 (including alpha emitting transuranics with half-lives greater than 5 years). This report discusses these radionuclides and other radionuclides that may be significant during a radiological performance assessment analysis of an LLW disposal facility. This report not only includes essential information on each radionuclide, but also incorporates waste and disposal information on the radionuclide, and behavior of the radionuclide in the environment and in the human body. Radionuclides addressed in this document include technetium-99, carbon-14, iodine-129, tritium, cesium-137, strontium-90, nickel-59, plutonium-241, nickel-63, niobium-94, cobalt-60, curium -42, americium-241, uranium-238, and neptunium-237.

NONE

1996-11-01T23:59:59.000Z

420

CHARACTERISTICS Nitrated compounds constitute a  

E-Print Network [OSTI]

compounds. If there is a chance of an explosive reaction, conduct the operation behind a blast shield

Wilcock, William

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


421

Identifying Mixed Chemical and Radioactive Waste Mixed waste is: any waste material containing both radioactive materials  

E-Print Network [OSTI]

Identifying Mixed Chemical and Radioactive Waste Mixed waste is: any waste material containing both as noted on the list, you do not have a mixed waste and it may be managed as a normal radioactive waste radioactive waste after initially dating the container, the hold for decay time is extended, but you cannot

Straight, Aaron

422

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

SciTech Connect (OSTI)

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

NONE

1995-07-05T23:59:59.000Z

423

Boronated porphyrin compounds  

DOE Patents [OSTI]

A compound is described having the structure ##STR1## where R preferably is ##STR2## and most preferably R.sup.3 is a closo-carborane and R.sup.2 is --H, an alkyl or aryl having 1 to about 7 carbon atoms, This invention was made with Government support under NIH Grant No. CA-37961 awarded by the Department of Health and Human Services and under the Associated Universities Inc. Contract No. De-AC02-76CH00016 with the U.S. Department of Energy. The Government has rights in this invention.

Kahl, Stephen B. (Portola Valley, CA); Koo, Myoung-Seo (San Francisco, CA)

1992-01-01T23:59:59.000Z

424

Boronated porphyrin compounds  

DOE Patents [OSTI]

A compound is described having the structure ##STR1## where R preferably is ##STR2## and most preferably R.sup.3 is a closo-carborane and R.sup.2 is --H, an alkyl or aryl having 1 to about 7 carbon atoms, This invention was made with Government support under NIH Grant No. CA-37961 awarded by the Department of Health and Human Services and under the Associated Universities Inc. Contract No. De-AC02-76CH00016 with the U.S. Department of Energy. The Government has rights in this invention.

Kahl, S.B.; Koo, M.S.

1992-09-22T23:59:59.000Z

425

Geodatabase of the South Texas Uranium District  

E-Print Network [OSTI]

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

Mark Beaman; William Wade Mcgee

426

The Quest for the Heaviest Uranium Isotope  

E-Print Network [OSTI]

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

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

2012-01-17T23:59:59.000Z

427

The multiphoton ionization of uranium hexafluoride  

SciTech Connect (OSTI)

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

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

1992-05-01T23:59:59.000Z

428

Radiological health aspects of uranium milling  

SciTech Connect (OSTI)

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

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

1983-05-01T23:59:59.000Z

429

Investigation of Trace Uranium in Biological Matrices  

E-Print Network [OSTI]

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

Miller, James Christopher

2013-05-31T23:59:59.000Z

430

Distinguishing Between Site Waste, Natural, and Other Sources of Contamination at Uranium and Thorium Contaminated Sites - 12274  

SciTech Connect (OSTI)

Uranium and thorium processing and milling sites generate wastes (source, byproduct, or technically enhanced naturally occurring material), that contain contaminants that are similar to naturally occurring radioactive material deposits and other industry wastes. This can lead to mis-identification of other materials as Site wastes. A review of methods used by the US Army Corps of Engineers and the Environmental Protection Agency to distinguish Site wastes from potential other sources, enhanced materials, and natural deposits, at three different thorium mills was conducted. Real case examples demonstrate the importance of understanding the methods of distinguishing wastes. Distinguishing between Site wastes and enhanced Background material can be facilitated by establishing and applying a formal process. Significant project cost avoidance may be realized by distinguishing Site wastes from enhanced NORM. Collection of information on other potential sources of radioactive material and physical information related to the potential for other radioactive material sources should be gathered and reported in the Historical Site Assessment. At a minimum, locations of other such information should be recorded. Site decision makers should approach each Site area with the expectation that non site related radioactive material may be present and have a process in place to distinguish from Site and non Site related materials. (authors)

Hays, David C. [United States Army Corps of Engineers, Kansas City, Missouri, 64106 (United States)

2012-07-01T23:59:59.000Z

431

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

E-Print Network [OSTI]

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

American Society for Testing and Materials. Philadelphia

2008-01-01T23:59:59.000Z

432

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

E-Print Network [OSTI]

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

Lam, Oanh Phi

2010-01-01T23:59:59.000Z

433

Bioindicators for Monitoring Radioactive Pollution of the  

E-Print Network [OSTI]

* IK s Dfc2looX|o Risø-R-443 Bioindicators for Monitoring Radioactive Pollution of the Marine-R-443 BIOINDICATORS FOR MONITORING RADIOACTIVE POLLUTION OF THE MARINE ENVIRONMENT Experiments Dahlgaard Abstract. Mussels (Mytilus edulis) are globally used as bio- indicators for pollution of coastal

434

4. Nuclei and Radioactivity Paradoxes and Puzzles  

E-Print Network [OSTI]

, and Firearms tests wine, gin, whisky, and vodka for radioactivity. If the product does not have sufficient. The key feature of radioactivity that makes it so fascinating is that the energy released is enormous-- at least when compared to typical chemical energies. The typical energy release in the explosion of one

Browder, Tom

435

Radioactivity in Food and the Environment, 2004  

E-Print Network [OSTI]

Radioactivity in Food and the Environment, 2004 RIFE - 10 2005 #12;Food Standards Agency Emergency Planning, Radiation and Incidents Division Aviation House 125 Kingsway London WC2B 6NH RadioactivityinFoodandtheEnvironment,2004 Scottish Environment ProtectionAgency Radioactive Substances Unit Erskine Court The Castle

436

Radioactivity in Food and the Environment, 2002  

E-Print Network [OSTI]

Radioactivity in Food and the Environment, 2002 RIFE - 8 2003 #12;1 ENVIRONMENT AGENCY ENVIRONMENT AND HERITAGE SERVICE FOOD STANDARDS AGENCY SCOTTISH ENVIRONMENT PROTECTION AGENCY Radioactivity in Food and the Environment, 2002 RIFE - 8 October 2003 #12;2 This report was compiled by the Centre for Environment

437

Rev August 2006 Radiation Safety Manual Section 14 Radioactive Waste  

E-Print Network [OSTI]

Rev August 2006 Radiation Safety Manual Section 14 ­ Radioactive Waste Page 14-1 Section 14 Radioactive Waste Contents A. Proper Collection, Disposal, and Packaging and Putrescible Animal Waste.........................14-8 a. Non-Radioactive Animal Waste

Wilcock, William

438

Radioactivity studies in Lowestoft: the first fifty years  

E-Print Network [OSTI]

; it was renamed Windscale to avoid confusion with the uranium factory at Springfields. The site at Drigg had also

439

Apparatus and method for radioactive waste screening  

DOE Patents [OSTI]

An apparatus and method relating to screening radioactive waste are disclosed for ensuring that at least one calculated parameter for the measurement data of a sample falls within a range between an upper limit and a lower limit prior to the sample being packaged for disposal. The apparatus includes a radiation detector configured for detecting radioactivity and radionuclide content of the of the sample of radioactive waste and generating measurement data in response thereto, and a collimator including at least one aperture to direct a field of view of the radiation detector. The method includes measuring a radioactive content of a sample, and calculating one or more parameters from the radioactive content of the sample.

Akers, Douglas W.; Roybal, Lyle G.; Salomon, Hopi; Williams, Charles Leroy

2012-09-04T23:59:59.000Z

440

Thermal treatment of organic radioactive waste  

SciTech Connect (OSTI)

The organic radioactive waste which is generated in nuclear and isotope facilities (power plants, research centers and other) must be treated in order to achieve a waste form suitable for long term storage and disposal. Therefore the resulting waste treatment products should be stable under influence of temperature, time, radioactivity, chemical and biological activity. Another reason for the treatment of organic waste is the volume reduction with respect to the storage costs. For different kinds of waste, different treatment technologies have been developed and some are now used in industrial scale. The paper gives process descriptions for the treatment of solid organic radioactive waste of low beta/gamma activity and alpha-contaminated solid organic radioactive waste, and the pyrolysis of organic radioactive waste.

Chrubasik, A.; Stich, W. [NUKEM GmbH, Alzenau (Germany)

1993-12-31T23:59:59.000Z

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


441

Comparison of potential radiological consequences from a spent-fuel repository and natural uranium deposits  

SciTech Connect (OSTI)

A general criterion has been suggested for deep geological repositories containing spent fuel - the repositories should impose no greater radiological risk than due to naturally occurring uranium deposits. The following analysis investigates the rationale of that suggestion and determines whether current expectations of spent-fuel repository performance are consistent with such a criterion. In this study, reference spent-fuel repositories were compared to natural uranium-ore deposits. Comparisons were based on intrinsic characteristics, such as radionuclide inventory, depth, proximity to aquifers, and regional distribution, and actual and potential radiological consequences that are now occurring from some ore deposits and that may eventually occur from repositories and other ore deposits. The comparison results show that the repositories are quite comparable to the natural ore deposits and, in some cases, present less radiological hazard than their natural counterparts. On the basis of the first comparison, placing spent fuel in a deep geologic repository apparently reduces the hazard from natural radioactive materials occurring in the earth's crust by locating the waste in impermeable strata without access to oxidizing conditions. On the basis of the second comparison, a repository constructed within reasonable constraints presents no greater hazard than a large ore deposit. It is recommended that if the naturally radioactive environment is to be used as a basis for a criterion regarding repositories, then this criterion should be carefully constructed. The criterion should be based on the radiological quality of the waters in the immediate region of a specific repository, and it should be in terms of an acceptable potential increase in the radiological content of those waters due to the existence of the repository.

Wick, O.J.; Cloninger, M.O.

1980-09-01T23:59:59.000Z

442

New insights into uranium (VI) sol-gel processing  

SciTech Connect (OSTI)

Nuclear Magnetic Resonance (NMR) investigations on the Oak Ridge National Laboratory process for sol-gel synthesis of microspherical nuclear fuel (UO{sub 2}), has been extremely useful in sorting out the chemical mechanism in the sol-gel steps. {sup 13}C, {sup 15}N, and {sup 1}H NMR studies on the HMTA gelation agent (Hexamethylene tetramine, C{sub 6}H{sub 12}N{sub 4}) has revealed near quantitative stability of this adamantane-like compound in the sol-gel process, contrary to its historical role as an ammonia source for gelation from the worldwide technical literature. {sup 17}O NMR of uranyl (UO{sub 2}{sup ++}) hydrolysis fragments produced in colloidal sols has revealed the selective formation of a uranyl trimer, ((UO{sub 2}){sub 3}({mu}{sub 3}-O)({mu}{sub 2}-OH){sub 3}){sup +}, induced by basic hydrolysis with the HMTA gelation agent. Spectroscopic results will be presented to illustrate that trimer condensation occurs during sol-gel processing leading to layered polyanionic hydrous uranium oxides in which HMTAH{sup +} is occluded as an intercalation'' cation. Subsequent sol-gel processing of microspheres by ammonia washing results in in-situ exchange and formation of a layered hydrous ammonium uranate with a proposed structural formula of (NH{sub 4}){sub 2} ((UO{sub 2}){sub 8} O{sub 4} (OH){sub 10}) {center dot} 8H{sub 2}O. This compound is the precursor to sintered UO{sub 2} ceramic fuel. 23 refs., 10 figs.

King, C.M.; Thompson, M.C.; Buchanan, B.R. (Westinghouse Savannah River Co., Aiken, SC (USA)); King, R.B. (Georgia Univ., Athens, GA (USA). Dept. of Chemistry); Garber, A.R. (South Carolina Univ., Columbia, SC (USA). Dept. of Chemistry)

1990-01-01T23:59:59.000Z

443

2010 Annual Planning Summary for Civilian Radioactive Waste Management...  

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

Civilian Radioactive Waste Management (CRWM) 2010 Annual Planning Summary for Civilian Radioactive Waste Management (CRWM) Annual Planning Summaries briefly describe the status of...

444

Fiscal Year 2007 Civilian Radioactive Waste Management Fee Adequacy...  

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

Fiscal Year 2007 Civilian Radioactive Waste Management Fee Adequacy Assessment Report Fiscal Year 2007 Civilian Radioactive Waste Management Fee Adequacy Assessment Report U.S....

445

Office of Civilian Radioactive Waste Management-Quality Assurance...  

Office of Environmental Management (EM)

Office of Civilian Radioactive Waste Management-Quality Assurance Requirements and Description Office of Civilian Radioactive Waste Management-Quality Assurance Requirements and...

446

Lab obtains approval to begin design on new radioactive waste...  

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

New radioactive waste staging facility Lab obtains approval to begin design on new radioactive waste staging facility The 4-acre complex will include multiple staging buildings...

447

Letter to Congress RE: Office of Civilian Radioactive Waste Management...  

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

to Congress RE: Office of Civilian Radioactive Waste Management's Annual Financial Report Letter to Congress RE: Office of Civilian Radioactive Waste Management's Annual Financial...

448

Radioactive Material Use at the EMSL Radiochemistry Annex  

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

Dispersible radioactive material must be placed in rigid, leak- tight inner containers (e.g., durable screw-top sample jars). Non-dispersible radioactive material may...

449

Southwestern Low-Level Radioactive Waste Disposal Compact (South Dakota)  

Broader source: Energy.gov [DOE]

This legislation authorizes the state's entrance into the Southwestern Low-Level Radioactive Waste Disposal Compact, which provides for the cooperative management of low-level radioactive waste....

450

Portsmouth Site Delivers First Radioactive Waste Shipment to...  

Office of Environmental Management (EM)

Portsmouth Site Delivers First Radioactive Waste Shipment to Disposal Facility in Texas Portsmouth Site Delivers First Radioactive Waste Shipment to Disposal Facility in Texas...

451

RESRAD Computer Code- Evaluation of Radioactively Contaminated Sites  

Broader source: Energy.gov [DOE]

The evaluation of sites with radioactive contamination was a problem until the RESidual RADioactivity (RESRAD) Computer Code was first released in 1989.

452

EIS-0200: Managing Treatment, Storage, and Disposal of Radioactive...  

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

00: Managing Treatment, Storage, and Disposal of Radioactive and Hazardous Waste EIS-0200: Managing Treatment, Storage, and Disposal of Radioactive and Hazardous Waste SUMMARY This...

453

Baseline risk assessment of ground water contamination at the Uranium Mill Tailings Site near Maybell, Colorado  

SciTech Connect (OSTI)

The US Department of Energy (DOE) Uranium Mill Tailings Remedial Action (UMTRA) Project consists of the Surface Project (Phase I) and the Ground Water Project (Phase II). Under the UMTRA Surface Project, tailings, radioactive contaminated soil, building foundations, and materials associated with the former processing of uranium ore at UMTRA sites are placed into disposal cells. The cells are designed to reduce radon and other radiation emissions and to prevent further contamination of ground water. One UMTRA Project site is near Maybell, Colorado. Surface cleanup at this site is under way and is scheduled for completion in 1996. The tailings are being stabilized in-place at this site. The disposal area has been withdrawn from public use by the DOE and is referred to as the permanent withdrawal area. The Ground Water Project evaluates the nature and extent of ground water contamination resulting from past uranium ore processing activities. The Ground Water Project at this site is in its beginning stages. This report is a site-specific document that will be used to evaluate current and future potential impacts to the public and the environment from exposure to contaminated ground water. The results of this evaluation and further site characterization will determine whether any action is needed to protect human health or the environment. Currently, no points of exposure (e.g. a drinking water well); and no receptors of contaminated ground water have been identified at the Maybell site. Therefore, there are no current human health and ecological risks associated with exposure to contaminated ground water. Furthermore, if current site conditions and land- and water-use patterns do not change, it is unlikely that contaminated ground water would reach people or the ecological communities in the future.

NONE

1995-09-01T23:59:59.000Z

454

Baseline risk assessment of ground water contamination at the Uranium Mill Tailings Site near Naturita, Colorado  

SciTech Connect (OSTI)

The Uranium Mill Tailings Remedial Action (UMTRA) Project consists of the Surface Project (phase I), and the Ground Water Project (phase II). For the UMTRA Project site located near Naturita, Colorado (the Naturita site), phase I involves the removal of radioactively contaminated soils and materials and their transportation to a disposal site at Union Carbide Corporation`s Upper Burbank Repository at Uravan, Colorado, about 13 road miles (mi) (21 kilometers [km]) to the northwest. No uranium mill tailings are involved because the tailings were removed from the Naturita site and placed at Coke Oven, Colorado, during 1977 to 1979. Phase II of the project will evaluate the nature and extent of ground water contamination resulting from uranium processing and its effect on human health or the environment; and will determine site-specific ground water compliance strategies in accordance with the US Environmental Protection Agency (EPA) ground water standards established for the UMTRA Project. Human health risks could occur from drinking water pumped from a hypothetical well drilled in the contaminated ground water area. Environmental risks may result if plants or animals are exposed to contaminated ground water, or surface water that has received contaminated ground water. Therefore, a risk assessment is conducted for the Naturita site. This risk assessment report is the first site-specific document prepared for the Ground Water Project at the Naturita site. What follows is an evaluation of current and possible future impacts to the public and the environment from exposure to contaminated ground water. The results of this evaluation and further site characterization will be used to determine whether any action is needed to protect human health or the environment.

NONE

1995-08-01T23:59:59.000Z

455

Current issues (and problems) in uranium mine and mill site remediation  

SciTech Connect (OSTI)

The environmental impact of the mining and milling of uranium ores is similar to that of traditional metal mining with the added factor of the characteristic radioactivity in uranium ores. Residues of these ores therefore generate specific potential hazards requiring special precautions on a site specific basis, as well as special regulatory procedures and controls to ensure protection of public health and safety in the long term. There are strong indications that on a global scale U-mining tailings management and remediation-activities are steadily becoming governed by the ultimate goal of sustainable stabilization and re-establishment of a healthy environment, rather than by immediate or short term needs. In Central Europe rehabilitation of uranium mining and milling districts has only started. Some problems are listed as follows: (1) Limitation, long term control and prediction of aquatic and atmospheric dispersal of contaminants from tailings impoundments, waste rock dumps and abandoned underground mines, (2) Dewatering of tailings (large volumes), (3) Design of cover systems and inhibition of microbian process, (4) Controlled flooding of extensive underground mine workings and related prognosis and control of containment dispersion, (5) Reduction of Rn-exhalation during the flooding process and after mine abandonment, in particular in areas close to densely populated regions, (6) Determination of long term radiological impacts on residents near sources of contamination and identification of natural background levels, (7) Identification of critical containment pathways that remain active, (8) Conception and implementation of a comprehensive monitoring system for all pathways which would operate on a long term basis, (9) Limitation of mine water drainage to be treated and decontaminated and of resulting sludges (in considerable quantities) to be disposed of and which would have to be classified as hazardous waste in the future due to their radionuclide content.

Quarch, H. [DSR GmbH, Saarbruecken (Germany); Kuhlmann, J.; Zettwoog, P. [CERTAC, Auffargis (France)

1994-12-31T23:59:59.000Z

456

Environmental assessment of remedial action at the slick rock Uranium Mill Tailings sites Slick Rock, Colorado  

SciTech Connect (OSTI)

The Uranium Mill Tailings Radiation Control Act of 1978 (42 USC {section} 7901 et seq.), hereafter referred to as the UMTRCA, authorized the U.S. Department of Energy (DOE) to clean up two uranium mill tailings processing sites near Slick Rock, Colorado, in San Miguel County. The purpose of the cleanup is to reduce the potential health effects associated with the radioactive materials remaining on the sites and on vicinity properties (VPs) associated with the sites. Contaminated materials cover an estimated 55 acres of the Union Carbide (UC) processing site and 12 ac of the North Continent (NC) processing site. The total estimated volume of contaminated materials is approximately 61 8,300 cubic yards. In addition to the contamination in the two processing site areas, four VPs were found to contain contamination. As a result of the tailings being exposed to the environment, contamination associated with the UC and NC sites has leached into shallow ground water. Surface water has not been affected. The closest residence is approximately 0.3 air mi from either site. The proposed action is to remediate the UC and NC sites by removing all contaminated materials within the designated site boundaries or otherwise associated with the sites, and relocating them to, and stabilizing them at, a location approximately 5 road mi (8 km) northeast of the sites on land administered by the Bureau of Land Management (BLM). Remediation would be performed by the DOE`s Uranium Mill Tailings Remedial Action (UMTRA) Project. All solid contaminated materials would be buried under 5 feet (ft) of rock and soil materials. The proposed disposal site area is currently used by ranchers for cattle grazing over a 7-month period. The closest residence to the proposed disposal site is 2 air mi. An estimated 44 ac of land would be permanently transferred from the BLM to the DOE and restricted from future use.

Not Available

1994-09-01T23:59:59.000Z

457

Incentives for the use of depleted uranium alloys as transport cask containment structure  

SciTech Connect (OSTI)

Radioactive material transport casks use either lead or depleted uranium (DU) as gamma-ray shielding material. Stainless steel is conventionally used for structural containment. If a DU alloy had sufficient properties to guarantee resistance to failure during both nominal use and accident conditions to serve the dual-role of shielding and containment, the use of other structure materials (i.e., stainless steel) could be reduced. (It is recognized that lead can play no structural role.) Significant reductions in cask weight and dimensions could then be achieved perhaps allowing an increase in payload. The mechanical response of depleted uranium has previously not been included in calculations intended to show that DU-shielded transport casks will maintain their containment function during all conditions. This paper describesa two-part study of depleted uranium alloys: First, the mechanical behavior of DU alloys was determined in order to extend the limited set of mechanical properties reported in the literature. The mechanical properties measured include the tensile behavior the impact energy. Fracture toughness testing was also performed to determine the sensitivity of DU alloys to brittle fracture. Fracture toughness is the inherent material property which quantifies the fracmm resistance of a material. Tensile strength and ductility are significant in terms of other failure modes, however, as win be discussed. These mechanical properties were then input into finite element calculations of cask response to loading conditions to quantify the potential for claiming structural credit for DU. (The term structural credit'' describes whether a material has adequate properties to allow it to assume a positive role in withstanding structural loadings.)

McConnell, P [GRAM, Inc., Albuquerque, NM (United States); Salzbrenner, R; Wellman, G W; Sorenson, K B [Sandia National Labs., Albuquerque, NM (United States)

1992-01-01T23:59:59.000Z

458

Characterization of past and present solid waste streams from the Plutonium-Uranium Extraction Plant  

SciTech Connect (OSTI)

During the next two decades the transuranic wastes, now stored in the burial trenches and storage facilities at the Hanford Site, are to be retrieved, processed at the Waste Receiving and Processing Facility, and shipped to the Waste Isolation Pilot Plant near Carlsbad, New Mexico for final disposal. Over 7% of the transuranic waste to be retrieved for shipment to the Waste Isolation Pilot Plant has been generated at the Plutonium-Uranium Extraction (PUREX) Plant. The purpose of this report is to characterize the radioactive solid wastes generated by PUREX using process knowledge, existing records, and oral history interviews. The PUREX Plant is currently operated by the Westinghouse Hanford Company for the US Department of Energy and is now in standby status while being prepared for permanent shutdown. The PUREX Plant is a collection of facilities that has been used primarily to separate plutonium for nuclear weapons from spent fuel that had been irradiated in the Hanford Site`s defense reactors. Originally designed to reprocess aluminum-clad uranium fuel, the plant was modified to reprocess zirconium alloy clad fuel elements from the Hanford Site`s N Reactor. PUREX has provided plutonium for research reactor development, safety programs, and defense. In addition, the PUREX was used to recover slightly enriched uranium for recycling into fuel for use in reactors that generate electricity and plutonium. Section 2.0 provides further details of the PUREX`s physical plant and its operations. The PUREX Plant functions that generate solid waste are as follows: processing operations, laboratory analyses and supporting activities. The types and estimated quantities of waste resulting from these activities are discussed in detail.

Pottmeyer, J.A.; Weyns, M.I.; Lorenzo, D.S.; Vejvoda, E.J. [Los Alamos Technical Associates, Inc., NM (US); Duncan, D.R. [Westinghouse Hanford Co., Richland, WA (US)

1993-04-01T23:59:59.000Z

459

Determination of thorium, uranium, and potassium elemental concentrations in surface soils in Cyprus  

E-Print Network [OSTI]

A comprehensive study was conducted to determine thorium, uranium and potassium elemental concentrations in surface soils throughout the accessible area of Cyprus using high-resolution gamma-ray spectrometry. A total of 115 soil samples was collected from all over the bedrock surface of the island based on the different lithological units of the study area. The soil samples were sieved through a fine mesh, sealed in 1000-mL plastic Marinelli beakers, and measured in the laboratory in terms of their gamma radioactivity for a counting time of 18 hours each. From the measured gamma-ray spectra, elemental concentrations were determined for thorium (range from 2.5x10^-3 to 9.8 micro g g-1), uranium (from 8.1x10^-4 to 3.2 micro g g-1) and potassium (from 1.3x10^-4 to 1.9 %). The Arithmetic mean values (A.M. +- S.D.) calculated are (1.2 +- 1.7) micro g g-1, (0.6 +- 0.7) micro g g-1, and (0.4 +- 0.3) %, for thorium, uranium and potassium, respectively, which are by a factor of three to six lower than the world average values of 7.4 micro g g-1 (Th), 2.8 micro g g-1 (U) and 1.3 % (K) derived from all data available worldwide. The best-fitting relation between the concentrations of Th and K versus U, and also of K versus Th, is essentially of linear type with a correlation coefficient of 0.93, 0.84, and 0.90, respectively. The Th/U, K/U, and K/Th ratios (slopes) calculated are equal to 2.0, 2.8x10^3,and 1.4x10^3, respectively.

Michalis Tzortzis; Haralabos Tsertos

2004-03-15T23:59:59.000Z

460

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

SciTech Connect (OSTI)

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

NONE

1996-08-01T23:59:59.000Z

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461

Uranium Mill Tailings Remedial Action Project, fiscal year 1995 annual report to stakeholders  

SciTech Connect (OSTI)

In 1978, Congress authorized the DOE to assess and clean up contamination at 24 designated former uranium processing sites. The DOE is also responsible for cleaning up properties in the vicinity of the sites where wind and water erosion deposited tailings or people removed them from the site for use in construction or landscaping projects. Cleanup is being undertaken in cooperation with state governments and Indian tribes within whose boundaries the sites are located. It is being conducted in two phases: the surface project and the ground water project. This report addresses specifics about both phases of the UMTRA Project. DOE`s UMTRA Project is the world`s largest materials management project ever undertaken to reduce or eliminate risk to the general public from exposure to potentially hazardous and radioactive materials. With an estimated cost at completion of nearly $2 billion for both phases of the UMTRA Project, and with the responsibility for encapsulating and isolating almost one-fourth of all the uranium mill tailings generated across the entire US (more than 44 million cubic yards), the UMTRA Project and its people have achieved a long record of safely and effectively completing its mission. It continually enhances its national reputation through its diligent process and cost efficiency as well as its international recognition for its technological innovation.

NONE

1995-09-30T23:59:59.000Z

462

Progress Toward Remediation of Uranium Tailings in Mailuu-Suu, Kyrgyzstan  

SciTech Connect (OSTI)

The town of Mailuu-Suu in Kyrgyzstan inherited 23 distinct tailings deposits from Soviet-Era uranium mining operations. Mailuu-Suu is located in the narrow landslide-prone valley of the Mailuu-Suu River about 25 km from the Uzbekistan border. Large-scale release of the radioactive tailings, as a result of landslides, could lead to irreversible contamination of the river and downstream areas. The Mailuu-Suu River is a tributary to the Syr-Darya River, the Fergana valley's main source of irrigation water. The Fergana Valley is a key agricultural region and major population center that spans Kyrgyzstan, Tajikistan, and Uzbekistan. The trans-boundary nature of the Mailuu-Suu tailings issue presents an opportunity for collaboration among these Central Asian states. A cooperative approach to addressing environmental issues such as Mailuu-Suu may contribute to the region's stability by facilitating peaceful associations. Experience from remediation of sites in the US under the Uranium Mill Tailings Remediation Action Project (UMTRA) will be useful in progressing toward remediation at Mailuu-Suu.

Buckley, P B; Ranville, J; Honeyman, B D; Smith, D K; Rosenberg, N; Knapp, R B

2003-07-09T23:59:59.000Z

463

Summary report on reprocessing evaluation of selected inactive uranium mill tailings sites  

SciTech Connect (OSTI)

Sandia National Laboratories has been assisting the Department of Energy in the Uranium Mill Tailings Remedial Actions Program (UMTRAP) the purpose of which is to implement the provisions of Title I of Public Law 95-604, Uranium Mill Tailings Radiation Control Act of 1978.'' As part of this program, there was a need to evaluate the mineral concentration of the residual radioactive materials at some of the designated processing sites to determine whether mineral recovery would be practicable. Accordingly, Sandia contracted Mountain States Research and Development (MSRD), a division of Mountain States Mineral Enterprises, to drill, sample, and test tailings at 12 sites to evaluate the cost of and the revenue that could be derived from mineral recovery. UMTRAP related environmental and engineering sampling and support activities were performed in conjunction with the MSRD operations. This summary report presents a brief description of the various activities in the program and of the data and information obtained and summarizes the results. 8 refs., 9 tabs.

Not Available

1983-09-01T23:59:59.000Z

464

Environmental assessment of remedial action at the Gunnison Uranium Mill Tailings Site, Gunnison, Colorado. [UMTRA Project  

SciTech Connect (OSTI)

This document assesses and compares the environmental impacts of various alternatives for remedial action at the Gunnison uranium of mill tailings site located 0.5 miles south of Gunnison, Colorado. The site covers 56 acres and contains 35 acres of tailings, 2 of the original mill buildings and a water tower. The Uranium Mill Tailings Radiation Control of Act of 1978 (UMTRCA), Public Law 95-604, authorizes the US Department of Energy to clean up the site to reduce the potential health impacts associated with the residual radioactive materials remaining at the site and at associated (vicinity) properties off the site. The US Environmental Protection Agency promulgated standards for the remedial actions (40 CFR 192). Remedial actions must be performed in accordance with these standards and with the occurrence of the Nuclear Regulatory Commission. Four alternatives have been addressed in this document. The first alternative is to consolidate the tailings and associated contaminated soils into a recontoured pile on the southern portion of the existing site. A radon barrier of silty clay would be constructed over the pile and various erosion control measures would be taken to assure the long-term integrity of the pile. Two other alternatives which involve moving the tailings to new locations are assessed in this document. These alternatives generally involve greater short-term impacts and are more costly but would result in the tailings being stabilized in a location farther from the city of Gunnison. The no action alternative is also assessed.

Bachrach, A.; Hoopes, J.; Morycz, D. (Jacobs Engineering Group, Inc., Pasadena, CA (USA)); Bone, M.; Cox, S.; Jones, D.; Lechel, D.; Meyer, C.; Nelson, M.; Peel, R.; Portillo, R.; Rogers, L.; Taber, B.; Zelle, P. (Weston (Roy F.), Inc., Washington, DC (USA)); Rice, G. (Sergent, Hauskins and Beckwith (USA))

1984-12-01T23:59:59.000Z

465

Summary of Uranium Solubility Studies in Concrete Waste Forms and Vadose Zone Environments  

SciTech Connect (OSTI)

One of the methods being considered for safely disposing of Category 3 low-level radioactive wastes is to encase the waste in concrete. Concrete encasement would contain and isolate the waste packages from the hydrologic environment and act as an intrusion barrier. The current plan for waste isolation consists of stacking low-level waste packages on a trench floor, surrounding the stacks with reinforced steel, and encasing these packages in concrete. These concrete-encased waste stacks are expected to vary in size with maximum dimensions of 6.4 m long, 2.7 m wide, and 4 m high. The waste stacks are expected to have a surrounding minimum thickness of 15 cm of concrete encasement. These concrete-encased waste packages are expected to withstand environmental exposure (solar radiation, temperature variations, and precipitation) until an interim soil cover or permanent closure cover is installed and to remain largely intact thereafter. Any failure of concrete encasement may result in water intrusion and consequent mobilization of radionuclides from the waste packages. This report presents the results of investigations elucidating the uranium mineral phases controlling the long-term fate of uranium within concrete waste forms and the solubility of these phases in concrete pore waters and alkaline, circum-neutral vadose zone environments.

Golovich, Elizabeth C.; Wellman, Dawn M.; Serne, R. Jeffrey; Bovaird, Chase C.

2011-09-30T23:59:59.000Z

466

Method for production of an isotopically enriched compound  

DOE Patents [OSTI]

A method is presented for producing and isolating an isotopically enriched compound of a desired isotope from a parent radionuclide. The method includes forming, or placing, a precipitate containing a parent radionuclide of the desired daughter isotope in a first reaction zone and allowing sufficient time for the parent to decay into the desired gaseous daughter radioisotope. The method further contemplates collecting the desired daughter isotope as a solid in a second reaction zone through the application of temperatures below the freezing point of the desired isotope to a second reaction zone that is connected to the first reaction zone. Specifically, a method is presented for producing isotopically enriched compounds of xenon, including the radioactive isotope Xe-131m and the stable isotope Xe-131.

Watrous, Matthew G.

2012-12-11T23:59:59.000Z

467

Baseline risk assessment of ground water contamination at the uranium mill tailings site near Riverton, Wyoming. Revision 1  

SciTech Connect (OSTI)

The Uranium Mill Tailings Remedial Action (UMTRA) Project consists of two phases: the Surface Project and the Ground Water Project. At the UMTRA Project site near Riverton, Wyoming, Surface Project cleanup occurred from 1988 to 1990. Tailings and radioactively contaminated soils and materials were taken from the Riverton site to a disposal cell in the Gas Hills area, about 60 road miles (100 kilometers) to the east. The surface cleanup reduces radon and other radiation emissions and minimizes further ground water contamination. The UMTRA Project`s second phase, the Ground Water Project, will evaluate the nature and extent of ground water contamination at the Riverton site that has resulted from the uranium ore processing activities. Such evaluations are used at each site to determine a strategy for complying with UMTRA ground water standards established by the US Environmental Protection Agency (EPA) and if human health risks could result from exposure to ground water contaminated by uranium ore processing. Exposure could hypothetically occur if drinking water were pumped from a well drilled in an area where ground water contamination might have occurred. Human health and environmental risks may also result if people, plants, or animals are exposed to surface water that has mixed with contaminated ground water.

NONE

1995-09-01T23:59:59.000Z