WorldWideScience

Sample records for uranium complex obtained

  1. Phospholyl-uranium complexes

    International Nuclear Information System (INIS)

    Gradoz, Philippe

    1993-01-01

    After having reported a bibliographical study on penta-methylcyclopentadienyl uranium complexes, and a description of the synthesis and radioactivity of uranium (III) and (IV) boron hydrides compounds, this research thesis reports the study of mono and bis-tetramethyl-phospholyl uranium complexes comprising chloride, boron hydride, alkyl and alkoxide ligands. The third part reports the comparison of structures, stabilities and reactions of homologue complexes in penta-methylcyclopentadienyl and tetramethyl-phospholyl series. The last part addresses the synthesis of tris-phospholyl uranium (III) and (IV) complexes. [fr

  2. Uranium thiolate complexes

    International Nuclear Information System (INIS)

    Leverd, Pascal C.

    1994-01-01

    This research thesis proposes a new approach to the chemistry of uranium thiolate complexes as these compounds are very promising for various uses (in bio-inorganic chemistry, in some industrial processes like oil desulphurization). It more particularly addresses the U-S bond or more generally bonds between polarizable materials and hard metals. The author thus reports the study of uranium organometallic thiolates (tricyclo-penta-dienic and mono-cyclo-octa-tetraenylic complexes), and of uranium homoleptic thiolates (tetra-thiolate complexes, hexa-thiolate complexes, reactivity of homoleptic thiolate complexes) [fr

  3. Obtain of uranium concentrates from fertil liquids

    International Nuclear Information System (INIS)

    Narvaez Castillo, W.A.

    1992-01-01

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

  4. Uranium nucleophilic carbene complexes

    International Nuclear Information System (INIS)

    Tourneux, Jean-Christophe

    2012-01-01

    The only stable f-metal carbene complexes (excluding NHC) metals f present R 2 C 2- groups having one or two phosphorus atoms in the central carbon in alpha position. The objective of this work was to develop the chemistry of carbenes for uranium (metal 5f) with the di-anion C{Ph 2 P(=S)} 2 2- (SCS 2- ) to extend the organometallic chemistry of this element in its various oxidation states (+3-+6), and to reveal the influence of the 5f orbitals on the nature and reactivity of the double bond C=U. We first isolated the reactants M(SCHS) (M = Li and K) and demonstrated the role of the cation M + on the evolution of the di-anion M 2 SCS (M = Li, K, Tl) which is transformed into LiSCHS in THF or into product of intramolecular cyclization K 2 [C(PhPS) 2 (C 6 H 4 )]. We have developed the necessary conditions mono-, bis- and tris-carbene directly from the di-anion SCS 2- and UCl 4 , as the precursor used in uranium chemistry. The protonolysis reactions of amides compounds (U-NEt 2 ) by the neutral ligand SCH 2 S were also studied. The compounds [Li(THF)] 2 [U(SCS)Cl 3 ] and [U(SCS)Cl 2 (THF) 2 ] were then used to prepare a variety of cyclopentadienyl and mono-cyclo-octa-tetra-enyliques uranium(IV) carbene compounds of the DFT analysis of compounds [M(SCS)Cl 2 (py) 2 ] and [M(Cp) 2 (SCS)] (M = U, Zr) reveals the strong polarization of the M=C double bond, provides information on the nature of the σ and π interactions in this binding, and shows the important role of f orbitals. The influence of ancillary ligands on the M=C bond is revealed by examining the effects of replacing Cl - ligands and pyridine by C 5 H 5 - groups. Mulliken and NBO analyzes show that U=C bond, unlike the Zr=C bond, is not affected by the change in environment of the metal center. While the oxidation tests of carbene complexes of U(IV) were disappointing, the first carbene complex of uranium (VI), [UO 2 (SCS)(THF) 2 ], was isolated with the uranyl ion UO 2 2+ . The reactions of compounds UO 2 X 2

  5. Uranium extraction by complexation with siderophores

    Science.gov (United States)

    Bahamonde Castro, Cristina

    One of the major concerns of energy production is the environmental impact associated with the extraction of natural resources. Nuclear energy fuel is obtained from uranium, an abundant and naturally occurring element in the environment, but the currently used techniques for uranium extraction leave either a significant fingerprint (open pit mines) or a chemical residue that alters the pH of the environment (acid or alkali leaching). It is therefore clear that a new and greener approach to uranium extraction is needed. Bioleaching is one potential alternative. In bioleaching, complexants naturally produced from fungi or bacteria may be used to extract the uranium. In the following research, the siderophore enterobactin, which is naturally produced by bacteria to extract and solubilize iron from the environment, is evaluated to determine its potential for complexing with uranium. To determine whether enterobactin could be used for uranium extraction, its acid dissociation and its binding strength with the metal of interest must be determined. Due to the complexity of working with radioactive materials, lanthanides were used as analogs for uranium. In addition, polyprotic acids were used as structural and chemical analogs for the siderophore during method development. To evaluate the acid dissociation of enterobactin and the subsequent binding constants with lanthanides, three different analytical techniques were studied including: potentiometric titration, UltraViolet Visible (UV-Vis) spectrophotometry and Isothermal Titration Calorimetry (ITC). After evaluation of three techniques, a combination of ITC and potentiometric titrations was deemed to be the most viable way for studying the siderophore of interest. The results obtained from these studies corroborate the ideal pH range for enterobactin complexation to the lanthanide of interest and pave the way for determining the strength of complexation relative to other naturally occurring metals. Ultimately, this

  6. Uranium complex recycling method of purifying uranium liquors

    International Nuclear Information System (INIS)

    Elikan, L.; Lyon, W.L.; Sundar, P.S.

    1976-01-01

    Uranium is separated from contaminating cations in an aqueous liquor containing uranyl ions. The liquor is mixed with sufficient recycled uranium complex to raise the weight ratio of uranium to said cations preferably to at least about three. The liquor is then extracted with at least enough non-interfering, water-immiscible, organic solvent to theoretically extract about all of the uranium in the liquor. The organic solvent contains a reagent which reacts with the uranyl ions to form a complex soluble in the solvent. If the aqueous liquor is acidic, the organic solvent is then scrubbed with water. The organic solvent is stripped with a solution containing at least enough ammonium carbonate to precipitate the uranium complex. A portion of the uranium complex is recycled and the remainder can be collected and calcined to produce U 3 O 8 or UO 2

  7. Synthesis and reactivity of triscyclopentadienyl uranium (III) and (IV) complexes

    International Nuclear Information System (INIS)

    Berthet, J.C.

    1992-01-01

    The reactions of (RC 5 H 4 ) 3 U with R=trimethylsilylcyclopentadienyl or tertiobutylcyclopentadienyl are studied for the synthesis of new uranium organometallic compounds. Reactions with sodium hydride are first described uranium (III) anionic hydrides obtained are oxidized for synthesis of stable uranium (IV) organometallic hydrides. Stability of these compounds is discussed. Reactivity of these uranium (III) and (IV) hydrides are studied. Formation of new binuclear compounds with strong U-O and U-N bonds is examined and crystal structure are presented. Monocyclooctatetraenylic uranium complexes are also investigated

  8. Methods for obtaining sorption data from uranium-series disequilibria

    International Nuclear Information System (INIS)

    Finnegan, D.L.; Bryant, E.A.

    1987-12-01

    Two possible methods have been identified for obtaining in situ retardation factors from measurements of uranium-series disequilibria at Yucca Mountain. The first method would make use of the enhanced 234 U/ 238 U ratio in groundwater to derive a signature for exchangeable uranium sorbed on the rock; the exchangeable uranium would be leached and assayed. The second method would use the ratio of 222 Rn to 234 U in solution, corrected for weathering, to infer the retardation factor for uranium. Similar methods could be applied to thorium and radium

  9. U3O8 obtained from metallic uranium

    International Nuclear Information System (INIS)

    Lopez, Marisol; Gonzalez, Alfredo; Pasqualini, Enrique E.

    2003-01-01

    Enriched uranium oxide, U 3 O 8 , used as nuclear powder in MTR's, can be obtained by direct oxidation of metallic uranium at 800 C degrees. Maximum density, 8.2 gr/cm 3 , is achieved after grinding and a high temperature treatment at 1400 C degrees. All the process is highly controllable and performed in dry environments. (author)

  10. Simulation of uranium and plutonium oxides compounds obtained in plasma

    Science.gov (United States)

    Novoselov, Ivan Yu.; Karengin, Alexander G.; Babaev, Renat G.

    2018-03-01

    The aim of this paper is to carry out thermodynamic simulation of mixed plutonium and uranium oxides compounds obtained after plasma treatment of plutonium and uranium nitrates and to determine optimal water-salt-organic mixture composition as well as conditions for their plasma treatment (temperature, air mass fraction). Authors conclude that it needs to complete the treatment of nitric solutions in form of water-salt-organic mixtures to guarantee energy saving obtainment of oxide compounds for mixed-oxide fuel and explain the choice of chemical composition of water-salt-organic mixture. It has been confirmed that temperature of 1200 °C is optimal to practice the process. Authors have demonstrated that condensed products after plasma treatment of water-salt-organic mixture contains targeted products (uranium and plutonium oxides) and gaseous products are environmental friendly. In conclusion basic operational modes for practicing the process are showed.

  11. Towards new developments in uranium chemistry. Scientific report presented to obtain and Accreditation to Supervise Research

    International Nuclear Information System (INIS)

    Berthet, Jean-Claude

    2003-01-01

    After a presentation of his academic curriculum, the author proposes an overview of some of his main research activities and works which notably addressed the reactivity of uranium III complexes (synthesis and reactivity of uranium hydride complexes, synthesis of poly-metallic complexes), amide complexes (synthesis of uranium IV amide precursors, reactivity of cationic complexes, synthesis of uranium IV complexes), uranium triflate (or trifluoromethanesulfonate) complexes, the synthesis of U(Cot)X_2(L)_n complexes and of their derivatives, the complexing of lanthanide iodides and triflates

  12. Phthalocyaninato complexes of thorium, protactinium and uranium

    International Nuclear Information System (INIS)

    Beck, O.F.

    1985-01-01

    For the preparation of Bis(phthalocyaninato)-actinoid(IV) complexes, AnPc 2 , a new optimizing synthesis procedure was developed, with which it was possible to prepare spectrally pure, that is, H 2 Pc-free, ThPc 2 , UPc 2 and the isostructurally similar 231 PaPc 2 .PaPc 2 . This was verified with the help of electron spectra, which were compared to preparations which were synthesized in another manner. The corresponding perfluorinated compounds were also produced for thorium and uranium by use of tetrafluorophthalic acid nitrile instead of phthalic acid nitrile as initial product. Electron and infrared spectra show the typical bands of the non-substituted complexes. By the attempt to produce a mono(phthalocyaninato)-thorium complex with the use of ThI 4 as initial material a pyridine-extracted pure ThPcI 2 (py) 2 was obtained with a typical mono(phthalocyaninato) complex electron spectrum, an extremely moisture sensitive compound which in water or acids decomposes and produces H 2 Pc. (orig./RB) [de

  13. Structure of some complex halides of uranium(III)

    International Nuclear Information System (INIS)

    Volkov, V.A.; Suglobova, I.G.; Chirkst, D.E.

    1987-01-01

    Polycrystals of some halide complexes of uranium(III) were obtained and investigated by x-ray diffraction. The M 2 UCl 5 compounds (M = K, Rb) are isostructural with K 2 PrCl 5 ; RbU 2 Cl 7 is of the same type as RbDy 2 Cl 7 or KDy 2 Cl 7 . The coordination number of the uranium is 7. The M 2 UBr 5 compounds (M = K-Cs) are isostructural with Cs 2 DyCl 5 , and the coordination number of the uranium is 6. Rb 2 NaUCl 6 is a 12L-hexagonal polytype, the structural analog of Cs 2 NaCrF 6 . The most characteristic coordination number of uranium in the UHal 3 -MHal systems is 8 for Hal = F, 7 for Hal = Cl, and 6 for Hal = Br

  14. Obtaining of uranium tetrafluoride UF4 by electrodialysis reactive from uranium concentrates

    International Nuclear Information System (INIS)

    Munoz Lay, Danny Mauricio

    2014-01-01

    The generation of uranium fuels has always been a topic worldwide. The uranium fuel manufacturing base is made under very strict parameters of radiological and industrial safety, being a stage called 'nuclear fuel cycle'. In Chile, it is done constant research for fuels. This report focuses primarily on participating in such research; mainly in the production of uranium tetrafluoride (UF 4 ) .The tetrafluoride production is very crucial for the nuclear fuel industry. Its production varies from precipitation in stirred conditions to electrolysis in mercury. However, both processes has shortcomings either in performance and environmental pollution, which is why it is proposed a new method of production based on a friendly process to the environment and easier to operate, the reactive electrodialysis (RED). Electrodialysis is a hybrid reactive process of separation by membranes, cationic and / or anionic, namely, ionic species. In the process, ions are induced to move by an electric potential applied and separated by these membranes, a highly selective physical barrier which allows passage of ions with certain charge, and prevents the passage of oppositely charged ions. And in turn, it is reactive because it forces a chemical reaction, redox, to obtain uranium tetrafluoride (UF 4 ). The results of these experiments show that by reactive electrodialysis, NH 4 UF 5 deposits were obtained. However, calcinating the NH 4 UF 5 to 450 o C, it decomposes to obtain uranium tetrafluoride, UF 4 . The best working conditions were obtained with an electric current of 0.5 (A), 41 o C and a flow of 16 (ml / s) of the electrolyte. It was possible to obtain 5,995 (g) to 3 (h), giving a current efficiency of 71.42%. In turn, working at high temperatures and flow recirculation is possible to operate with a potential difference of 1.7 (V)

  15. Cordilleran metamorphic core complexes and their uranium favorability

    International Nuclear Information System (INIS)

    Coney, P.J.; Reynolds, S.J.

    1980-11-01

    The objective of this report is to provide a descriptive body of knowledge on Cordilleran metamorphic core complexes including their lithologic and structural characteristics, their distribution within the Cordillera, and their evolutionary history and tectonic setting. The occurrence of uranium in the context of possibility for uranium concentration is also examined. This volume contains appendices of the following: annotated bibliography of Cordilleran metamorphic core complexes; annotated bibliography of the uranium favorability of Cordilleran metamorphic core complexes; uranium occurrences in the Cordilleran metamorphic core complex belt; and geology, uranium favorability, uranium occurrences and tectonic maps of individual Cordilleran metamorphic core complexes; and locations, lithologic descriptions, petrographic information and analytical data for geochemical samples

  16. Complex defects in the oxidation of uranium

    International Nuclear Information System (INIS)

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

    1986-01-01

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

  17. Uranium

    International Nuclear Information System (INIS)

    Hamdoun, N.A.

    2007-01-01

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

  18. Macrocyclic ligands for uranium complexation

    International Nuclear Information System (INIS)

    Potts, K.T.

    1991-04-01

    A highly preorganized 24-macrocycle containing biuret, thiobiuret and pyridine subunits has been prepared by high dilution ring-closure procedures. Intermediate products to this macrocycle have been utilized to extend this synthetic route to include further representatives where solubility and stability will be influenced by substituent variation. A 1:1 complex has been formed from uranyl acetate and a quinquepyridine derivative, this representing a new type of ligand for the uranyl ion. A very convenient synthetic procedure that will allow the incorporation of these macrocycles into polymeric systems has been developed for the introduction of a vinyl substituent into the 4-position of the pyridine ring. Using triflate, vinyltributyltin and Pd 0 chemistry, this procedure should make a variety of substituted 4-vinylpyridines available for the first time. 3 refs

  19. Obtaining uranium and/or vanadium values from solutions

    Energy Technology Data Exchange (ETDEWEB)

    Vojkovic, M

    1982-04-22

    A process for the recovery of at least one of uranium and vanadium from an aqueous liquor is claimed. It comprises: (a) treating the liquor with a low molecular weight completely water-miscible solvent selected from the group consisting of methanol, iso-propyl alcohol or acetone to form at least two phases; (b) separating the phases; (c) recovering the solvent from the first phase as the azeotropic solvent/water mixture by simple, non-fractional distillation and recycling the mixture to step (a); and (d) recovering metal values from a second one of the phases.

  20. Introduction. Physicochemical aspects of uranium concentrates obtaining from the wastes and raw materials

    International Nuclear Information System (INIS)

    Mirsaidov, I.U.

    2014-01-01

    The uranium deposits of Tajikistan played an immensely significant role in the practical solution of a radioactive raw materials problem which appeared during the post-World War II years in the USSR. The pioneer in this field became complex №6 (currently known as 'Vostokredmet'). The first soviet uranium was produced from the ores extracted from the republic's deposits. For 50 years (1945-1995 y.), uranium bearing raw materials from all over the former USSR were delivered to Tajikistan, and uranium oxide was produced, which was later delivered back to Russia for further production of enriched uranium. The total volume of uranium produced in Tajikistan plants was approximately 100 thousands tons. In Sughd region, during that period, more than 55 million tons of uranium waste was accumulated. The total activity of the waste, according to different calculations, is approximately 240-285 TBq. The total amount of waste in dumps and tailings piles is estimated to be more than 170 million tons, most of which are located in the neighborhoods of hydrometallurgical plants and heap leaching locations. Uranium industry wastes in Northern Tajikistan have become attractive for different investors and commercial companies, from secondary reprocessing of mines and tailings' point of view, since the uranium price is increasing. In this regard, research on developing uranium extraction methods from wastes is broadening. The study of the possibility and economic reasonability of reprocessing former year's dumps requires comprehensive examination, and relates not only to uranium extraction but to safe extraction of dumps from tailings as well.

  1. A method for the electrolytic coating of uranium or uranium alloy parts, and parts thus obtained

    International Nuclear Information System (INIS)

    1973-01-01

    A method, preceded by a surface treatment, for applying an electrolytic coating (e.g. of nickel) on uranium, or uranium alloy parts. This method is characterized in that the previous surface treatment comprises a chemical removal of grease in halogenated solvent bath (free from halogen ions) and an anodic scouring in a buffered aqueous solution solution of an acid free from halogen ions. The coating can be applied to fuel elements for nuclear industry, counter-weight for aeronautics and space industries and to radiation shields [fr

  2. Uranium hetero-bimetallic complexes: synthesis, structure and magnetic properties

    International Nuclear Information System (INIS)

    Le Borgne, Th.

    2000-01-01

    The aim of this thesis is to synthesize molecular complexes with uranium and transition metal ions in close proximity, to determine the nature of the magnetic interaction between them. We decided to use Schiff bases as assembling ligands, which are unusual for uranium (IV). Although the simplest Schiff bases, such as H 2 Salen, lead to ligand exchange reactions, the bi-compartmental Schiff base H 4 L 6 (bis(3-hydroxy-salicylidene) - 2,2-dimethyl-propylene) allows the crystal structure determination of the complex [L 6 Cu(pyr)]U[L 6 Cu].2pyr, obtained by reaction of the metallo-ligand H 2 L 6 Cu with U(acac) 4 . In this manner, the complexes [L 6 Co(pyr)] 2 U and [L 6 Ni(pyr)] 2 U.pyr were also isolated, as well as the compounds in which the paramagnetic ions have been exchanged by the diamagnetic ions Zn II , Zr IV and Th IV ': [L 6 Zn(pyr)] 2 U, [L 6 Cu] 2 Zr and [L 6 Cu(pyr)]Th[L 6 Cu].2pyr. These complexes are the first which involve three metallic centres assembling by the means of a hexa-dentate Schiff base. The crystalline structures show, for all these complexes, the outstanding orthogonal arrangement of the two fragments L 6 M around the central atom which is in a dodecahedral environment of eight oxygen atoms of two Schiff bases. The syntheses of the isostructural complexes Cu2 II and Zn 2 U in which the uranium (IV) ion is close, in the first one, to the paramagnetic ion Cu II and, in the second one, to the diamagnetic ion Zn II , has allowed the use of the empiric method to determine the nature of the magnetic interaction between an f element and a transition metal. The comparison of the magnetic behaviour of two complexes Cu 2 U and Zn 2 U, expressed by the variation of χT vs T, reveals the ferromagnetic interaction in the heart of the triad Cu-U-Cu. The magnetic behaviour of the complexes Cu 2 Th et Cu 2 Zr which does not show any coupling between the two copper (II) ions and the weak antiferromagnetic interaction in the Ni 2 U compound, favour the

  3. Uranium

    International Nuclear Information System (INIS)

    Poty, B.; Cuney, M.; Bruneton, P.; Virlogeux, D.; Capus, G.

    2010-01-01

    concentration in peat bogs, deposits combined with marine phosphates, with coal and lignite, with black shales, with carbonate rocks, deposits in Precambrian quartz pebble conglomerates, basal-type deposits, deposits in sandstones (tabular, roll-type and tectono-lithologic deposits), breccia chimney filling deposits, deposits in metamorphic rocks, metasomatic deposits, deposits in intrusive rocks, deposits associated with hematite breccia complexes, deposits in granitic rocks, deposits in volcanic rocks, deposits in proterozoic discordances (Athabasca basin, Pine Creek geo-syncline); 4 - French uranium bearing areas and deposits: history of the French uranium mining industry, geological characteristics of French deposits (black shales, sandstones, granites), abroad success of French mining companies (Africa, North America, South America, Australia, Asia); 5 - exploration and exploitation; 6 - uranium economy: perspectives of uranium demand, present day production status, secondary resources, possible resources, market balances, prices and trends, future availability and nuclear perspectives. (J.S.)

  4. Unique advantages of organometallic supporting ligands for uranium complexes

    Energy Technology Data Exchange (ETDEWEB)

    Diaconescu, Paula L. [Univ. of California, Los Angeles, CA (United States); Garcia, Evan [Univ. of California, Los Angeles, CA (United States)

    2014-05-31

    The objective of our research project was to study the reactivity of uranium complexes supported by ferrocene-based ligands. In addition, this research provides training of graduate students as the next generation of actinide scientists.

  5. Unique advantages of organometallic supporting ligands for uranium complexes

    International Nuclear Information System (INIS)

    Diaconescu, Paula L.; Garcia, Evan

    2014-01-01

    The objective of our research project was to study the reactivity of uranium complexes supported by ferrocene-based ligands. In addition, this research provides training of graduate students as the next generation of actinide scientists.

  6. Sintering of uranium dioxide obtained by continuous precipitation of AUC

    International Nuclear Information System (INIS)

    Amaya, C.D.; Sterba, M.E.; Russo, D.O.

    1993-01-01

    The Nuclear Materials Division in Bariloche Atomic Center evaluates the ceramic behaviour of UO 2 powders obtained from continuously precipitated and reduced AUC (Ammonium Uranyl Tri Carbonate). An analysis is made of powder characteristics (particle morphology and size distribution and specific area) on behaviour of UO 2 during sintering (compaction, sintering, pore and grain microstructure, etc.). 1 ref

  7. Alecto - results obtained with homogeneous critical experiments on plutonium 239, uranium 235 and uranium 233

    International Nuclear Information System (INIS)

    Bruna, J.G.; Brunet, J.P.; Caizegues, R.; Clouet d'Orval, Ch.; Kremser, J.; Tellier, H.; Verriere, Ph.

    1965-01-01

    In this report are given the results of the homogeneous critical experiments ALECTO, made on plutonium 239, uranium 235 and uranium 233. After a brief description of the equipment, the critical masses for cylinders of diameters varying from 25 to 42 cm, are given and compared with other values (foreign results, criticality guide). With respect to the specific conditions of neutron reflection in the ALECTO experiments the minimal values of critical masses are: Pu239 M c = 910 ± 10 g, U235 M c = 1180 ± 12 g and U233 M c = 960 ± 10 g. Experiments relating to cross sections and constants to be used on these materials are presented. Lastly, kinetic experiments allow to compare pulsed neutron methods to fluctuation methods [fr

  8. Ligand influences on properties of uranium coordination complexes. Structure, reactivity, and spectroscopy

    International Nuclear Information System (INIS)

    Kosog, Boris

    2012-01-01

    example of a uranium(IV) μ-trithiocarbonate was synthesized and characterized. Reaction of the μ-sulfide complex [{(( Ad ArO) 3 N)U IV } 2 (μ-S)], which is obtained by reaction of the uranium(III) complex with triphenylphosphine sulfide, with CS 2 leads to the formation of the [{(( Ad ArO) 3 N)U IV } 2 (μ-κ 2 :κ 2 -CS 3 )]. The coordination mode of the trithicarbonate differes from that of the respective carbonate, obtained previously from a similar reaction of the μ-oxo complex with CO 2 . With the help of detailed DFT calculations, the different reactivity of uranium(III) towards CO 2 and CS 2 is rationalized. Finally, a series of the first uranium vinyl complexes is presented. These are obtained through inter- and intramolecular C-C-coupling reactions of terminal mono- or bisalkynes on a uranium(III) complex. Detailed mechanistic DFT calculations show that a bimetallic mechanism is energetically most likely. This mechanism can be transferred to the catalytic alkyne coupling using both uranium(III), as reported by Eisen in the late 90's, and also transition metal catalyzed C-C-coupling, where a bimetallic mechanism should be taken into account.

  9. Cordilleran metamorphic core complexes and their uranium favorability. Final report

    International Nuclear Information System (INIS)

    Coney, P.J.; Reynolds, S.J.

    1980-11-01

    The objective of this report is to provide a descriptive body of knowledge on Cordilleran metamorphic core complexes including their lithologic and structural characteristics, their distribution within the Cordillera, and their evolutionary history and tectonic setting. The occurrence of uranium in the context of possibility for uranium concentration is also examined. Chapter 1 is an overview of Cordilleran metamorphic core complexes which describes their physical characteristics, tectonic setting and geologic history. This overview is accompanied by a tectonic map. Chapter 2 is a discussion of the mantled gneiss dome concept. The purpose of including this work is to provide a basic history of this concept and to describe the characteristics and distribution of gneiss domes throughout the world to enable one to compare and contrast them with the metamorphic core complexes as discussed in this report. Some gneiss domes are known producers of uranium (as are also some core complexes). Chapter 3 is an examination of the effects of the core complex process on adjacent sedimentary and volcanic cover terranes. Also included is a discussion of the kinematic significance of these cover terranes as they are related to process within the cores of the complexes. Some of the cover terranes have uranium prospects in them. Chapter 4 is a detailed discussion of uranium in Cordilleran metamorphic core complexes and includes the conceptual basis for the various types of occurrences and the processes that might favor concentration of uranium. The report is supported by a 5-part Appendix. The majority of the core complexes discussed in this report either do not appear or are not recognizable on existing published geologic maps

  10. The uranium potential of the Bushveld igneous complex

    International Nuclear Information System (INIS)

    Andreoli, M.A.G.; Hart, R.J.; Brynard, H.J.; Camisani-Calzolari, F.A.G.M.

    1987-06-01

    A review of published literature supported by field observations on the uranium potential of the Bushveld Complex indicates that this geological region may host deposits with reserves in the range of a few thousand tons U 3 O 8 . The possibility that the Bushveld Complex or its cover rocks hosts, or has ever hosted in the past, giant uranium deposits such as those of Olympic Dam, Key Lake, Jabiluka or Rossing is considered to be unlikely. The potential for volcanogenic, caldera-type deposits in the Rooiberg Felsites remains at present untested. Recommendations for research currently sponsored by the AEC at the University of Pretoria are presented

  11. Method of purifying uranium tetrafluoride hydrate and preparing uranium (VI) peroxide hydrate using a fluoride complexing agent

    International Nuclear Information System (INIS)

    Barreiro, A.J.; Lowe, C.M.T.; Lefever, J.A.; Pyman, R.L.

    1983-01-01

    The annual production of phosphate rock, on the order of about 30-40 million tons yearly, represents several million pounds of uranium. The present invention provides a process of purifying uranium tetrafluoride hydrate to produce a uranium (VI) peroxide product meeting 'yellow cake' standards using a double precipitation procedure. A fluoride complexing agent is used in the precipitation

  12. Uranium in 50 years? - Deeper, lower grade and more metallurgically complex? - 5312

    International Nuclear Information System (INIS)

    Polak, C.

    2015-01-01

    The economic exploitation of uranium deposits in the next 50 years will benefit from advances in mining and processing technology. The 'easiness' to find uranium deposits are a relic of the past. Exploration will need to make use of new technologies to help find blind or deep deposits. These issues are already being addressed by the uranium industry. Another issue will be to obtain social and environmental acceptation of the industry. To summarize the uranium mining industry is faced with 3 main challenges that are not necessarily mutually exclusive: deeper deposits, lower grades and chemically complex ores. The deposits of the next half of 21. century are likely to face at least one but potentially a combination of two or three of these challenges

  13. Recovery of enriched Uranium (20% U-235) from wastes obtained in the preparation of fuel elements for argonaut type reactors

    International Nuclear Information System (INIS)

    Uriarte, A.; Ramos, L.; Estrada, J.; del Val, J. L.

    1962-01-01

    Results obtained with the two following installations for recovering enriched uranium (20% U-235) from wastes obtained in the preparation of fuel elements for Argonaut type reactors are presented. Ion exchange unit to recover uranium form mother liquors resulting from the precipitation ammonium diuranate (ADU) from UO 2 F 2 solutions. Uranium recovery unit from solid wastes from the process of manufacture of fuel elements, consisting of a) waste dissolution, and b) extraction with 10% (v/v) TBP. (Author) 9 refs

  14. Uranium complexes with macrosyclic polyethers. Synthesis and structural chemical analysis

    International Nuclear Information System (INIS)

    Elbasyouny, A.

    1983-01-01

    This dissertation reports about studies on the chemical coordination behaviour of uranium of oxidation stages IV and VI with regard to twelve different macrocyclic ligands. For the preparation of the complexes, for every system a different method has been developed. The elementary analysis of the various complexes including the uranium had been done by X-ray fluorescence analysis, and the structural characterization proceeded via vibrational, uv-vis and emission spectroscopy as well as 1 H-NMR and 13 C-spin-lattice relaxation time studies. Conformational analysis of the polyethers used allowed the structural changes in the complexes to be observed. The structural analysis of the hydrous uranium VI crown ether complexes yielded information of characteristic features of these types of complexes. The first coordination sphere of the uranyl ion with covalently bonded anion remains unchanged. As to the water content, there is a certain range. Depending upon the solvent used, the complexes have two or four H 2 O molecules per formula unit. (orig./EF) [de

  15. More light on the U clan. [Uranium behaviour in complex ores

    Energy Technology Data Exchange (ETDEWEB)

    De Waal, S.A. (Potchefstroom Univ. for C.H.E. (South Africa). Dept. of Geology)

    1983-07-01

    A thorough knowledge of the geochemistry of uranium is necessary for the exploration and beneficiation of this mineral. At present we lack knowledge of the behaviour of uranium minerals in complex ores. This article deals with the geochemistry of uranium, its group identity, uranium minerals and the extraction mineralogy.

  16. Controlled thermolysis of uranium (alkoxy)siloxy complexes: a route to polymetallic complexes of Low-Valent uranium

    Energy Technology Data Exchange (ETDEWEB)

    Camp, Clement; Pecaut, Jacques; Mazzanti, Marinella [Laboratoire de Reconnaissance Ionique et Chimie de Coordination, SCIB, UMR-E3 CEA-UJF, INAC, CEA-Grenoble (France); Kefalidis, Christos E.; Maron, Laurent [LPCNO, CNRS et INSA, UPS, Universite de Toulouse (France)

    2013-07-01

    Decomposition into higher species: Intramolecular U{sup III}-mediated homolytic C-O bond cleavage in U{sup III} (alkoxy)siloxy complexes at low temperature and subsequent reduction with KC{sub 8} led to unprecedented polymetallic complexes containing siloxy, silanediolate, and silanetriolate ligands. Such compounds may be useful precursors to uranium ceramics relevant for catalysis and the storage of spent nuclear fuel. (Copyright copyright 2013 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  17. Nitrogen reduction and functionalization by a multimetallic uranium nitride complex

    Science.gov (United States)

    Falcone, Marta; Chatelain, Lucile; Scopelliti, Rosario; Živković, Ivica; Mazzanti, Marinella

    2017-07-01

    Molecular nitrogen (N2) is cheap and widely available, but its unreactive nature is a challenge when attempting to functionalize it under mild conditions with other widely available substrates (such as carbon monoxide, CO) to produce value-added compounds. Biological N2 fixation can do this, but the industrial Haber-Bosch process for ammonia production operates under harsh conditions (450 degrees Celsius and 300 bar), even though both processes are thought to involve multimetallic catalytic sites. And although molecular complexes capable of binding and even reducing N2 under mild conditions are known, with co-operativity between metal centres considered crucial for the N2 reduction step, the multimetallic species involved are usually not well defined, and further transformation of N2-binding complexes to achieve N-H or N-C bond formation is rare. Haber noted, before an iron-based catalyst was adopted for the industrial Haber-Bosch process, that uranium and uranium nitride materials are very effective heterogeneous catalysts for ammonia production from N2. However, few examples of uranium complexes binding N2 are known, and soluble uranium complexes capable of transforming N2 into ammonia or organonitrogen compounds have not yet been identified. Here we report the four-electron reduction of N2 under ambient conditions by a fully characterized complex with two UIII ions and three K+ centres held together by a nitride group and a flexible metalloligand framework. The addition of H2 and/or protons, or CO to the resulting complex results in the complete cleavage of N2 with concomitant N2 functionalization through N-H or N-C bond-forming reactions. These observations establish that a molecular uranium complex can promote the stoichiometric transformation of N2 into NH3 or cyanate, and that a flexible, electron-rich, multimetallic, nitride-bridged core unit is a promising starting point for the design of molecular complexes capable of cleaving and functionalizing N2 under

  18. Vibrational spectroscopy and structural analysis of complex uranium compounds (review)

    International Nuclear Information System (INIS)

    Umreiko, D.S.; Nikanovich, M.V.

    1985-01-01

    The paper reports on the combined application of experimental and theoretical methods of vibrational spectroscopy together with low-temperature luminescence data to determine the characteristic features of the formation and structure of complex systems, not only containing ligands directly coordinated to the CA uranium, but also associated with the extraspherical polyatomic electrically charged particles: organic cations. These include uranyl complexes and heterocyclical amines. Studied here were compounds of tetra-halouranylates with pyridine and its derivates, as well as dipyridyl, quinoline and phenanthroline. Structural schemes are also proposed for other uranyl complexes with protonated heterocyclical amines with a more complicated composition, which correctly reflect their spectroscopic properties

  19. Synthesis and reactivity of uranium (III) cyclopentadienyl complexes

    International Nuclear Information System (INIS)

    Foyentin, M.

    1987-01-01

    New uranium organometallic complexes are synthetized from the addition compound Cp U (THF). Reactions with lithium compounds, chlorides, alkynes and borohydrides. Oxidizing addition reactions are evidenced with alkyl halogenides. With a strong reducing agent, the complex Cp-UCH-Li allows the fixation and the reduction of nitrogen into ammonia. Lability of ligands bound to U (III) is evidenced, giving very reactive species and hence catalytic properties for these compounds. Catalytic hydrogenation of olefins is studied. Substitution reactions of alkyl groups of these complexes with olefins in presence or not of hydrogen or with alkyllithium are original [fr

  20. Study of the machining of uranium carbide rods obtained by continuous casting under electronic bombardment

    International Nuclear Information System (INIS)

    Rousset, P.; Accary, A.

    1965-01-01

    The authors consider the various methods of machining uranium mono-carbide and compare them critically in the case of their application to uranium carbide obtained by fusion under an electronic bombardment and continuous casting. This study leads them to propose two mechanical machining methods: cylindrical rectification and center-less rectification, preceded by a preliminary roughing out of a cylinder, the latter appearing more suitable. A study of the machining yields as a function of the diameter of the rough bars and of the diameter of the finished rods has shown that an optimum value of the rough bar diameter exists for each value of the finished rod diameter. It is found that the yield increases as the diameter itself increases, this yield rising from 45 per cent to around 70 per cent as the diameter of the rough bars increases from 25-26 mm to 37-38 mm. (authors) [fr

  1. The obtainment of highly concentrated uranium pellets for plate type (MTR) fuel by dispersion of uranium aluminides in aluminium

    International Nuclear Information System (INIS)

    Morando, R.A.; Raffaeli, H.A.; Balzaretti, D.E.

    1980-01-01

    The use of the intermetallic UAl 3 for manufacturing plate type MTR fuel with 20% U 235 enriched uranium and a density of about 20 kg/m 3 is analyzed. The technique used is the dispersion of UAl 3 particles in aluminium powder. The obtainment of the UAl 3 intermetallic was performed by fusion in an induction furnace in an atmosphere of argon at a pressure of 0.7 BAR (400 mm) using an alumina melting pot. To make the aluminide powder and attain the wished granulometry a cutting and a rotating crusher were used. Aluminide powders of different granulometries and different pressures of compactation were analyzed. In each case the densities were measured. The compacts were colaminated with the 'Picture Frame' technique at temperatures of 490 and 0 deg C with excellent results from the manufacturing view point. (M.E.L.) [es

  2. Radioactive effluents, Portsmouth Uranium Enrichment Complex, calendar year 1983

    International Nuclear Information System (INIS)

    Acox, T.A.; Klein, L.S.

    1984-03-01

    Radioactive discharges from the Portsmouth Uranium Enrichment Complex are discussed and tabulated. Tables indicate both the location of the discharge and the nuclides discharged. Routine discharges for 1983 are well below the Radioactive Concentration Guide limits specified in DOE Order 5480.1, Chapter XI. There was, however, an unplanned release in December from the X-326 Building Side Purge which exceeded the limits. 1 figure

  3. Evaluating the effectiveness of dilution of the recovered uranium with depleted uranium and low-enriched uranium to obtain fuel for VVER reactors

    International Nuclear Information System (INIS)

    Smirnov, A Yu; Sulaberidze, G A; Dudnikov, A A; Nevinitsa, V A

    2016-01-01

    The possibility of the recovered uranium enrichment in a cascade of gas centrifuges with three feed flows (depleted uranium, low-enriched uranium, recovered uranium) with simultaneous dilution of U-232,234,236 isotopes was shown. A series of numerical experiments were performed for different content of U-235 in low-enriched uranium. It has been demonstrated that the selected combination of diluents can simultaneously reduce the cost of separative work and the consumption of natural uranium, not only with respect to the previously used multi-flow cascade schemes, but also in comparison to the standard cascade for uranium enrichment. (paper)

  4. Study of new complexes of uranium and comba radical. I.- Complexes defective in sodium carbonate

    International Nuclear Information System (INIS)

    Vera Palomino, J.; Galiano Sedano, J. A.; Parellada Bellod, R.; Bellido Gonzalez, A.

    1975-01-01

    Some complexes formed in presence of defect of sodium carbonate with respect to the stoichiometric ratio (U): (C0 3 ) = 1:3 are studied. This ratio corresponds to the main complex which is responsible for the uranium extraction with CDMBAC organic solutions and from U(VI) aqueous solutions with an excess of sodium carbonate. (Author) 10 refs

  5. Synthesis of uranium and thorium dioxides by Complex Sol-Gel Processes (CSGP). Synthesis of uranium oxides by Complex Sol-Gel Processes (CSGP)

    International Nuclear Information System (INIS)

    Deptula, A.; Brykala, M.; Lada, W.; Olczak, T.; Wawszczak, D.; Chmielewski, A.G.; Modolo, G.; Daniels, H.

    2010-01-01

    In the Institute of Nuclear Chemistry and Technology (INCT), a new method of synthesis of uranium and thorium dioxides by original variant of sol-gel method - Complex Sol-Gel Process (CSGP), has been elaborated. The main modification step is the formation of nitrate-ascorbate sols from components alkalized by aqueous ammonia. Those sols were gelled into: - irregularly agglomerates by evaporation of water; - medium sized microspheres (diameter <150) by IChTJ variant of sol-gel processes by water extraction from drops of emulsion sols in 2-ethylhexanol-1 by this solvent. Uranium dioxide was obtained by a reduction of gels with hydrogen at temperatures >700 deg. C, while thorium dioxide by a simple calcination in the air atmosphere. (authors)

  6. Formation and uranium explorating prospect of sub-volcanic granitic complex and rich uranium ore deposit in South China

    International Nuclear Information System (INIS)

    Wang Yusheng

    1997-01-01

    The rich uranium ore deposits are all closely related to tecto-magmatism of late-magmatic cycle whether volcanic types or granitic types in south China. Volcanic type rich uranium deposit has closely relationship with sub-volcanic activity, and granitic type rich uranium deposit is also closely related to mid-fine, unequal particle small massif in late main invasion stage. Based on characteristics of magmatism, we name the rock sub-volcanic granite complex, which is a unique style and closely related to the formation of rich uranium ore deposit

  7. Uranium extraction from ores with lemon juice I,b-uranium recovery from pregnant lemon juice liquors obtained by attacking phosphate ores and suggested flowsheet

    International Nuclear Information System (INIS)

    EL-Sayed, M.H.

    1992-01-01

    In order to recover uranium from the pregnant liquors obtained by attacking safaga phosphate and qatrani phosphatic sandstone ore materials with lemon juice, methylation for acidic fraction-salt separation has been carried out. Afterwards, separation of uranium from the associated calcium (mainly present in lemon juice liquors as citrate) has been performed by making-use of the wide difference in their water solubility. The solutions containing the separated uranium were then subjected to evaporation till dryness whereby the precipitated uranyl citrate was calcined at 500 degree C to obtain the yellow orange oxide powder (U o 3 ). On the basis of one ton ore treatment, a flowsheet for uranium recovery from the two ore materials has been suggested

  8. Uranium extraction from ores with lemon juice; II,b. uranium recovery from pregnant lemon juice liquors obtained by attacking phosphate ore and suggested flowsheet

    International Nuclear Information System (INIS)

    Hussein, E.M.

    1997-01-01

    In order to recover uranium from the pregnant liquors obtained by attacking Safaga phosphate and Qatrani phosphatic sandstone ore materials with lemon juice, methylation for acidic fraction-salt separation has been carried out. Afterwards, separation of uranium from the associated calcium (mainly present in lemon juice liquors as citrate) has been performed by making-use of the wide difference in their water solubility. The solutions containing the separated uranium were then subjected to evaporation till dryness whereby the precipitated uranyl citrate was calcined at 500 degree C to obtain the yellow orange oxide powder (UO 3 ). On the basis of one ton ore treatment, a flowsheet for uranium recovery from the two ore materials has been suggested

  9. Determination of the stability constants of uranium-tetracycline complexes

    International Nuclear Information System (INIS)

    Tarenzi, L.R.; Saiki, M.

    1983-01-01

    Stability constants of complexes formed with tetracycline (TC) and uranium have been determined by solvent extraction technique. The site on the tetracycline molecule at which uranyl ion may be bound has been studied by means of potentiometric titration and spectrophotometric techniques. The complex species with 1:1 and 1:2 for UO 2 : TC ratio have been identified by conductometric titration. Solvent extraction studies have also shown that the complexes are mononuclear of the type UO 2 (TC) sub (n) (n=1,2) and that no hidroxocomplexes or negatively charged complexes have been formed. Stability constant values have been calculated by numerical weighted least square method and by graphical methods of two parameters, of the average number of ligands and of the limiting value. (Author) [pt

  10. Recovery of enriched Uranium (20% U-235) from wastes obtained in the preparation of fuel elements for argonaut type reactors

    Energy Technology Data Exchange (ETDEWEB)

    Uriarte, A; Ramos, L; Estrada, J; Val, J L. del

    1962-07-01

    Results obtained with the two following installations for recovering enriched uranium (20% U-235) from wastes obtained in the preparation of fuel elements for Argonaut type reactors are presented. Ion exchange unit to recover uranium form mother liquors resulting from the precipitation ammonium diuranate (ADU) from UO{sub 2}F{sub 2} solutions. Uranium recovery unit from solid wastes from the process of manufacture of fuel elements, consisting of a) waste dissolution, and b) extraction with 10% (v/v) TBP. (Author) 9 refs.

  11. Process for the winning of a concentrate containing uranium and purified phosphoric acid, as well as the concentrate containing uranium and purified phosphoric acid obtained by this process

    International Nuclear Information System (INIS)

    1980-01-01

    The uranium containing concentrate and purified phosphoric acid are obtained by treating wet phosphoric acid with an inorganic fluorine compound (ammonium fluoride) and an aliphatic ketone (acetone) in the presence of a reducing agent (finely divided iron). The ketone is added first and the formed uranium precipitate is separated from the solution. If the fluorine compound is added first, the yield is lowered by a factor of 2. (Th.P.)

  12. Investigations on the elution behaviour of TOPO complexes of uranium and thorium using supercritical fluid chromatography

    International Nuclear Information System (INIS)

    Kumar, R.; Sivaraman, N.; Srinivasan, T.G.; Vasudeva Rao, P.R.

    2004-01-01

    In summary uranium and thorium could be separated by supercritical fluid chromatography technique as their TOPO complexes. The elution profiles with pre-complexation of the metal nitrate indicate a better separation than the in-situ complexation. The technique can also be employed for the assay of uranium and thorium at low levels

  13. Biotransformation of uranium and transition metal citrate complexes by clostridia

    International Nuclear Information System (INIS)

    Francis, A.J.; Joshi-Tope, G.A.; Dodge, C.J.; Gillow, J.B.

    2002-01-01

    Clostridium sphenoides, which uses citric acid as its sole carbon source, metabolized equimolar Fe(III)-citrate with the degradation of citric acid and the reduction of Fe(III) to Fe(II), but not the U(VI)-citrate complex. However, in the presence of excess citric acid or added glucose it was reduced to U(IV)-citrate. In contrast, Clostridium sp., which ferments glucose but not citrate, reduced Fe(III)-citrate to Fe(II)-citrate and U(VI)-citrate to U(IV)-citrate only when supplied with glucose. These results show that complexed uranium is readily accessible as an electron acceptor despite the bacterium's inability to metabolize the organic ligand complexed to the actinide. These results also show that the metabolism of the metal-citrate complex depends upon the type of complex formed between the metal and citric acid. Fe(III) forms a bidentate complex with citric acid and was metabolized, whereas U forms a binuclear complex with citric acid and was recalcitrant. (author)

  14. Vibrational spectroscopy and structural analysis of uranium complexes

    Energy Technology Data Exchange (ETDEWEB)

    Umrejko, D.S.; Nikanovich, M.V.

    1984-12-01

    On the basis of experimental and theoretical studies of vibbrational spectra for halides, sulfates, phosphates, uranyl oxalates (and uranium) as well as for more complicated complex systems, reliable spectroscopic criteria have been established for estimation of their structural features by more simple and accessible (than direct) methods. Due to coordination to a central ion of U/sup 6/(U/sup 4/) ligands a geometry variation specific for each method of addition occurs and concomitant redistribution of the force interaction in the mentioned system as well, which directly affects the variation of their frequency characteristics and vibration modes. On this ground stable indications of particular types of coordination for mono- and polyatomic groups (including bridge-type, characteristic of polymetric structures) are pointed out in the IR absorption and Raman spectra. In the investigated structures the predominant effect of coordination on the spectral properties of complexes, as compared with other factors (for example, outer-sphere binding) is established. The presence of water molecules in an interlayer space does not tell essentially on the state of polyatomic ligands with all donor atoms bound with the uranium central atom (particularly, in binary uranyl phosphates). In the presence of free oxygen atoms the H/sub 2/O effect can lead only to some shift of the maxima of separate bands and their additional weak splitting (in uranyl sulfates).

  15. Interactions of quercetin-uranium complexes with biomembranes and DNA

    Energy Technology Data Exchange (ETDEWEB)

    Attia, Enas Mohammed Hassan

    2014-07-21

    Uranium decontamination gains a great importance with the spread of nuclear waste in both soil and water systems across the planet. All known remediation methods of uranium can be exclusively based either on synthetic materials with high adsorbent power and known physical chemistry or life organisms by which the uranium eventually accumulated inside their tissues. In the present thesis, it was attempted to design a rational approach for uranyl removal primarily from waters using the reducing potential of quercetin, which is a plant-derived small organic molecules, along with its photochemical activities. Such approach, which is neither a fully synthetic nor an organism-based approach, was chosen here to avoid disadvantages with both traditional strategies. Here, complexation experiments were designed to assess the use of uranyl-quercetin complexes for the photoreduction of water-soluble U(VI) to insoluble U(IV) by comparing absorption properties of uranyl-quercetin complexes in acetone, water, and hydrophobic bilayer lipid vesicles. The UV-vis data show that uranyl quercetin complex can form in both hydrophobic and hydrophilic environments. In both cases the B-ring band in quercetin structure becomes reduced, red shifted and a pronounced absorption arises in the 400-500 nm range. Such data suggests that U(VI) binds at the 3-OH and 4-carbonyl of ring C of quercetin. Interestingly, the results of UV-Vis spectroscopy part hint at a crucial role of a stable or transiently ionized hydroxyl for the efficient uranyl-dependent photodegradation of quercetin. FTIR spectroscopy absorption changes further demonstrates that the UV-vis-spectroscopic changes are indeed accompanied by changes in the chemical structure of the complex as expected for a uranyl-dependent photodegradation. IR data thus suggest that U(VI) becomes reduced by the photoreaction, rather than merely changing its coordination shell. The frequency shifts in the C=C and C=O absorption range on the other hand

  16. Interactions of quercetin-uranium complexes with biomembranes and DNA

    International Nuclear Information System (INIS)

    Attia, Enas Mohammed Hassan

    2014-01-01

    Uranium decontamination gains a great importance with the spread of nuclear waste in both soil and water systems across the planet. All known remediation methods of uranium can be exclusively based either on synthetic materials with high adsorbent power and known physical chemistry or life organisms by which the uranium eventually accumulated inside their tissues. In the present thesis, it was attempted to design a rational approach for uranyl removal primarily from waters using the reducing potential of quercetin, which is a plant-derived small organic molecules, along with its photochemical activities. Such approach, which is neither a fully synthetic nor an organism-based approach, was chosen here to avoid disadvantages with both traditional strategies. Here, complexation experiments were designed to assess the use of uranyl-quercetin complexes for the photoreduction of water-soluble U(VI) to insoluble U(IV) by comparing absorption properties of uranyl-quercetin complexes in acetone, water, and hydrophobic bilayer lipid vesicles. The UV-vis data show that uranyl quercetin complex can form in both hydrophobic and hydrophilic environments. In both cases the B-ring band in quercetin structure becomes reduced, red shifted and a pronounced absorption arises in the 400-500 nm range. Such data suggests that U(VI) binds at the 3-OH and 4-carbonyl of ring C of quercetin. Interestingly, the results of UV-Vis spectroscopy part hint at a crucial role of a stable or transiently ionized hydroxyl for the efficient uranyl-dependent photodegradation of quercetin. FTIR spectroscopy absorption changes further demonstrates that the UV-vis-spectroscopic changes are indeed accompanied by changes in the chemical structure of the complex as expected for a uranyl-dependent photodegradation. IR data thus suggest that U(VI) becomes reduced by the photoreaction, rather than merely changing its coordination shell. The frequency shifts in the C=C and C=O absorption range on the other hand

  17. Rapid determination of fluoride in uranyl nitrate solution obtained in conversion process of uranium tetrafluoride

    International Nuclear Information System (INIS)

    Levin, R.; Feldman, R.; Sahar, E.

    1976-01-01

    In uranium production the conversion of impure uranium tetrafluoride by sodium hydroxide was chosen as a current process. A rapid method for determination of fluoride in uranyl-nitrate solution was developed. The method includes precipitation of uranium as diuranate, separation by centrifugation, and subsequent determination of fluoride in supernate by titration with thorium nitrate. Fluoride can be measured over the range 0.15-2.5 gr/gr U, with accuracy of +-5%, within 15 minutes. (author)

  18. Controlled thermolysis of uranium (alkoxy)siloxy complexes. A route to polymetallic complexes of low-valent uranium

    Energy Technology Data Exchange (ETDEWEB)

    Camp, Clement; Pecaut, Jacques; Mazzanti, Marinella [CEA-Grenoble (France). Lab. de Reconnaissance Ionique et Chimie de Coordination; Kefalidis, Christos E.; Maron, Laurent [Toulouse Univ. (France). LPCNO, CNRS et INSA, UPS

    2013-11-25

    Decomposition into higher species: Intramolecular U{sup III}-mediated homolytic C-O bond cleavage in U{sup III} (alkoxy)siloxy complexes at low temperature and subsequent reduction with KC{sub 8} led to unprecedented polymetallic complexes containing siloxy, silanediolate, and silanetriolate ligands (see example: U green, Si yellow, K blue, O red). Such compounds may be useful precursors to uranium ceramics relevant for catalysis and the storage of spent nuclear fuel. [German] Zerfall in hoehere Spezies: Die intramolekulare U{sup III}-vermittelte homolytische C-O-Spaltung in U{sup III}-(Alkoxy)siloxy-Komplexen bei tiefer Temperatur mit nachfolgender Reduktion mit KC{sub 8} fuehrte zu ungewoehnlichen Polymetallkomplexen mit Siloxy-, Silandiolat- und Silantriolatliganden (siehe Beispiel: U gruen, Si gelb, K blau, O rot). Solche Verbindungen sind nuetzliche Vorstufen von Urankeramiken, die fuer die Katalyse und fuer die Speicherung verbrauchter Kernbrennstoffe wichtig sind.

  19. Uranium mill tailings neutralization: contaminant complexation and tailings leaching studies

    International Nuclear Information System (INIS)

    Opitz, B.E.; Dodson, M.E.; Serne, R.J.

    1985-05-01

    Laboratory experiments were performed to compare the effectiveness of limestone (CaCO 3 ) and hydrated lime [Ca(OH) 2 ] for improving waste water quality through the neutralization of acidic uranium mill tailings liquor. The experiments were designed to also assess the effects of three proposed mechanisms - carbonate complexation, elevated pH, and colloidal particle adsorption - on the solubility of toxic contaminants found in a typical uranium mill waste solution. Of special interest were the effects each of these possible mechanisms had on the solution concentrations of trace metals such as Cd, Co, Mo, Zn, and U after neutralization. Results indicated that the neutralization of acidic tailings to a pH of 7.3 using hydrated lime provided the highest overall waste water quality. Both the presence of a carbonate source or elevating solution pH beyond pH = 7.3 resulted in a lowering of previously achieved water quality, while adsorption of contaminants onto colloidal particles was not found to affect the solution concentration of any constituent investigated. 24 refs., 8 figs., 19 tabs

  20. Coordination phenomena of cationic uranium(iv) complexes

    International Nuclear Information System (INIS)

    Rohwer, H.E.

    1974-12-01

    The coordination properties of the cationic uranium(IV) complexes UCl 3 + , UCl 2 2+ , UCl 3+ , and U 4+ were studied in a non-aqueous medium in the presence of perchlorate as counterion which, however, proved to coordinate to a much greater extent than expected. The strong neutral ligand, HMPA, could successively displace some of the perchlorates. An electrostatic model for the U(CIO 4 ) 4 -HMPA-acetone system compared favourably with the actual results. This emphasized the high ionic content in the bonding with actenoid cations, even with such a high charge as +4 . These conclusions are in agreement with studies 75 in which nitrate acts as counter ion. Correspondingly the uranium (IV) chemistry is characterized by the absence of typical 3d-organometallic chemistry, for example, strong bonding with CO, P(Phi) 3 etc, which strongly depends on covalent bonding. This stresses the fact that the d and f orbitals are not readily available for strong bond formation with the actenoids. 76

  1. Nanostructured Thin Films Obtained from Fischer Aminocarbene Complexes

    Directory of Open Access Journals (Sweden)

    Rosa E. Lazo-Jiménez

    2016-03-01

    Full Text Available The synthesis of four amphiphilic organometallic complexes with the general formula RC = M(CO5NH(CH215CH3, where R is a ferrocenyl 2(a-b or a phenyl 4(a-b group as a donor moiety and a Fischer carbene of chromium (0 or tungsten (0 as an acceptor group, are reported. These four push-pull systems formed Langmuir (L monolayers at the air-water interface, which were characterized by isotherms of surface pressure versus molecular area and compression/expansion cycles (hysteresis curves; Brewster angle microscopic images were also obtained. By using the Langmuir–Blodgett (LB method, molecular monolayers were transferred onto glass substrates forming Z-type multilayers. LB films were characterized through ultraviolet-visible spectroscopy, atomic force microscopy and X-ray diffraction techniques. Results indicated that films obtained from 2b complex [(Ferrocenyl(hexadecylaminemethylidene] pentacarbonyl tungsten (0 are the most stable and homogeneous; due to their properties, these materials may be incorporated into organic electronic devices.

  2. Nanostructured Thin Films Obtained from Fischer Aminocarbene Complexes

    Science.gov (United States)

    Lazo-Jiménez, Rosa E.; Ortega-Alfaro, M. Carmen; López-Cortés, José G.; Alvarez-Toledano, Cecilio; Chávez-Carvayar, José Á.; Ignés-Mullol, Jordi; González-Torres, Maykel; Carreón-Castro, Pilar

    2016-01-01

    The synthesis of four amphiphilic organometallic complexes with the general formula RC = M(CO)5NH(CH2)15CH3, where R is a ferrocenyl 2(a-b) or a phenyl 4(a-b) group as a donor moiety and a Fischer carbene of chromium (0) or tungsten (0) as an acceptor group, are reported. These four push-pull systems formed Langmuir (L) monolayers at the air-water interface, which were characterized by isotherms of surface pressure versus molecular area and compression/expansion cycles (hysteresis curves); Brewster angle microscopic images were also obtained. By using the Langmuir–Blodgett (LB) method, molecular monolayers were transferred onto glass substrates forming Z-type multilayers. LB films were characterized through ultraviolet-visible spectroscopy, atomic force microscopy and X-ray diffraction techniques. Results indicated that films obtained from 2b complex [(Ferrocenyl)(hexadecylamine)methylidene] pentacarbonyl tungsten (0) are the most stable and homogeneous; due to their properties, these materials may be incorporated into organic electronic devices. PMID:28773289

  3. Speciation of bioaccumulated uranium(VI) by Euglena mutabilis cells obtained by laser fluorescence spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Brockmann, Sina; Bernhard, Gert [Technical Univ. Dresden (Germany). Radiochemistry; Helmholtz-Zentrum Dresden-Rossendorf (HZDR) e.V., Dresden (Germany). Inst. of Resource Ecology; Arnold, Thuro [Helmholtz-Zentrum Dresden-Rossendorf (HZDR) e.V., Dresden (Germany). Inst. of Resource Ecology

    2014-07-01

    The ability of Euglena mutabilis cells - a unicellular protozoan with a flexible pellicle, which is typically found in acid mine drainage (AMD) environments - to bioaccumulate uranium under acid conditions was studied in batch sorption experiments at pH 3 and 4 using Na{sub 2}SO{sub 4} and NaClO{sub 4} as background media. It was found that axenic cultures of Euglena mutabilis Schmitz were able to bioaccumulate in 5 days 94.9 to 99.2% of uranium from a 1 x 10{sup -5} mol/L uranium solution in perchlorate medium and 95.1 to 95.9% in sodium sulfate medium, respectively. The speciation of uranium in solution and uranium bioaccumulated by Euglena mutabilis cells, were studied by laser induced fluorescence spectroscopy (LIFS). The LIFS investigations showed that the uranium speciation in the NaClO{sub 4} systems was dominated by free uranyl(VI) species and that the UO{sub 2}SO{sub 4} species was dominating in the Na{sub 2}SO{sub 4} medium. Fluorescence spectra of the bioaccumulated uranium revealed that aqueous uranium binds to carboxylic and/or (organo)phosphate groups located on the euglenid pellicle or inside the Euglena mutabilis cells. Reduced uranium immobilization rates of 0.93-1.43 mg uranium per g Euglena mutabilis biomass were observed in similar experiments, using sterile filtrated AMD waters containing, 4.4 x 10{sup -5} mol/L uranium. These lower rates were attributed to competition with other cations for available sorption sites. Additional LIFS measurements, however, showed that the speciation of the bioaccumulated uranium by the Euglena mutabilis cells was found to be identical with the uranium speciation found in the bioaccumulation experiments carried out in Na{sub 2}SO{sub 4} and NaClO{sub 4} media. The results indicate that Euglena mutabilis has the potential to immobilize aqueous uranium under acid condition and thus may be used in future as promising agent for immobilizing uranium in low pH waste water environments. (orig.)

  4. Speciation of bioaccumulated uranium(VI) by Euglena mutabilis cells obtained by laser fluorescence spectroscopy

    International Nuclear Information System (INIS)

    Brockmann, Sina; Bernhard, Gert; Helmholtz-Zentrum Dresden-Rossendorf; Arnold, Thuro

    2014-01-01

    The ability of Euglena mutabilis cells - a unicellular protozoan with a flexible pellicle, which is typically found in acid mine drainage (AMD) environments - to bioaccumulate uranium under acid conditions was studied in batch sorption experiments at pH 3 and 4 using Na 2 SO 4 and NaClO 4 as background media. It was found that axenic cultures of Euglena mutabilis Schmitz were able to bioaccumulate in 5 days 94.9 to 99.2% of uranium from a 1 x 10 -5 mol/L uranium solution in perchlorate medium and 95.1 to 95.9% in sodium sulfate medium, respectively. The speciation of uranium in solution and uranium bioaccumulated by Euglena mutabilis cells, were studied by laser induced fluorescence spectroscopy (LIFS). The LIFS investigations showed that the uranium speciation in the NaClO 4 systems was dominated by free uranyl(VI) species and that the UO 2 SO 4 species was dominating in the Na 2 SO 4 medium. Fluorescence spectra of the bioaccumulated uranium revealed that aqueous uranium binds to carboxylic and/or (organo)phosphate groups located on the euglenid pellicle or inside the Euglena mutabilis cells. Reduced uranium immobilization rates of 0.93-1.43 mg uranium per g Euglena mutabilis biomass were observed in similar experiments, using sterile filtrated AMD waters containing, 4.4 x 10 -5 mol/L uranium. These lower rates were attributed to competition with other cations for available sorption sites. Additional LIFS measurements, however, showed that the speciation of the bioaccumulated uranium by the Euglena mutabilis cells was found to be identical with the uranium speciation found in the bioaccumulation experiments carried out in Na 2 SO 4 and NaClO 4 media. The results indicate that Euglena mutabilis has the potential to immobilize aqueous uranium under acid condition and thus may be used in future as promising agent for immobilizing uranium in low pH waste water environments. (orig.)

  5. recovery of enriched uranium from waste solution obtained from fuel fabrication laboratories

    International Nuclear Information System (INIS)

    Othman, S.H.A.

    2003-01-01

    reversed-phase partition chromatography is shown to be a convenient and applicable method for the quantitative recovery of uranium (19.7% enriched with 235 U) from highly impure solution . the processing of uranium compounds for atomic energy project especially in FMPP(Egyptian fuel manufacture pilot plant) gives rise to a variety of wastes in which the uranium content is of considerable importance. the recovery of uranium from concentrated mother liquors produced from ADU (ammonium diuranate ) precipitation, as well as those due to ADU washing is studied in this work. column of poly-trifluoro-monochloro-ethilene (Kel-F) supporting tri-n-butyl-phosphate (TBP) retains uranium .impurities are eluted with 6.5 M HCl, and the uranium is eluted with water and the recovery of uranium is better than 94%. A mathematical model was suggested to stimulate the sorption process of uranium ions (or any other ion ) by column of solvent impregnated resin containing organic extractant (the same as the previous column) . An excellent agreement was founded between the experimental results and the mathematical model

  6. Study of uranium oxide milling in order to obtain nanostructured UC{sub x} target

    Energy Technology Data Exchange (ETDEWEB)

    Guillot, Julien, E-mail: guillotjulien@ipno.in2p3.fr [Institut de Physique Nucléaire CNRS/IN2P3 UMR 8608 – Université Paris Sud, F-91406 ORSAY Cedex (France); Tusseau-Nenez, Sandrine; Roussière, Brigitte; Barré-Boscher, Nicole [Institut de Physique Nucléaire CNRS/IN2P3 UMR 8608 – Université Paris Sud, F-91406 ORSAY Cedex (France); Brisset, François [ICMMO UMR 8182 CNRS – Université Paris Sud, F-91405 Orsay Cedex (France); Mhamed, Maher Cheikh; Lau, Christophe [Institut de Physique Nucléaire CNRS/IN2P3 UMR 8608 – Université Paris Sud, F-91406 ORSAY Cedex (France); Nowak, Sophie [ITODYS, Université Paris Diderot, Sorbonne Paris Cité, CNRS UMR-7086, F-75013 Paris (France); IPSL CNRS UMR 7583 Universités Paris Est Créteil et Paris Diderot, F-94010 Créteil Cedex (France)

    2016-05-01

    A R&D program is developed at the ALTO facility to provide new beams of exotic neutron-rich nuclei, as intense as possible. In the framework of European projects, it has been shown that the use of refractory targets with nanometric structure allows us to obtain beams of nuclei unreachable until now. The first parameter to be controlled in the processing to obtain targets with a homogeneous nanostructure is the grinding of uranium dioxide, down to 100 nm grain size. In this study, dry and wet grinding routes are studied and the powders are analyzed in terms of phase stabilization, specific surface area and grain morphology. It appears that the grinding, as well dry as wet, leads to the decrease of the particle size. The oxidation of UO{sub 2} is observed whatever the grinding. However, the dry grinding is the most efficient and leads to the oxidation of UO{sub 2} into U{sub 4}O{sub 9} and U{sub 3}O{sub 7} whose quantities increase with the grinding time while crystallite sizes decrease.

  7. Methods for obtaining distributions of uranium occurrence from estimates of geologic features

    International Nuclear Information System (INIS)

    Ford, C.E.; McLaren, R.A.

    1980-04-01

    The problem addressed in this paper is the determination of a quantitative estimate of a resource from estimates of fundamental variables which describe the resource. Due to uncertainty about the estimates, these basic variables are stochastic. The evaluation of random equations involving these variables is the core of the analysis process. The basic variables are originally described in terms of a low and a high percentile (the 5th and 95th, for example) and a central value (the mode, mean or median). The variable thus described is then generally assumed to be represented by a three-parameter lognormal distribution. Expressions involving these variables are evaluated by computing the first four central moments of the random functions (which are usually products and sums of variables). Stochastic independence is discussed. From the final set of moments a Pearson distribution is obtained; the high values of skewness and kurtosis resulting from uranium data require obtaining Pearson curves beyond those described in published tables. A cubic spline solution to the Pearson differential equation accomplishes this task. A sample problem is used to illustrate the application of the process; sensitivity to the estimated values of the basic variables is discussed. Appendices contain details of the methods and descriptions of computer programs

  8. Methods for obtaining distributions of uranium occurrence from estimates of geologic features

    International Nuclear Information System (INIS)

    Ford, C.E.; McLaren, R.A.

    1980-04-01

    The problem addressed in this report is the determination of a quantitative estimate of a resource from estimates of fundamental variables which describe the resource. Due to uncertainty about the estimates, these basic variables are stochastic. The evaluation of random equations involving these variables is the core of the analysis process. The basic variables are originally described in terms of a low and a high percentile (the 5th and 95th, for example) and a central value (the mode, mean or median). The variable thus described is then generally assumed to be represented by a three-parameter lognormal distribution. Expressions involving these variables are evaluated by computing the first four central moments of the random functions (which are usually products and sums of variables). Stochastic independence is discussed. From the final set of moments a Pearson distribution is obtained; the high values of skewness and kurtosis resulting from uranium data requires obtaining Pearson curves beyond those described in published tables. A cubic spline solution to the Pearson differential equation accomplishes this task. A sample problem is used to illustrate the application of the process; sensitivity to the estimated values of the basic variables is discussed. Appendices contain details of the methods and descriptions of computer programs

  9. Interest of uranium complexes for the mechanism study of the McMurry reaction

    International Nuclear Information System (INIS)

    Maury, O.

    1997-01-01

    The reducing coupling reactions of ketones in diols and olefins are generally carried out with titanium or samarium compounds. In this work uranium complexes have been used. They have allowed to study the chemical reaction mechanism. This thesis is divided into three parts: 1) the reduction mechanism of uranium tetrachloride by cyclic voltametry has been studied at first. It has been shown that this reduction is followed by a transfer reaction of chlorides between the reduced specie of the higher electronic density and UCl . 2) In the second part is described: the synthesis, the crystal structure, the reactivity of the chemical agents, the stereochemistry of diols and alkenes formation and the pinacolisation reaction catalysis. 3) In the last part, the limits of the McMurry reaction are given by the study of the aromatic ketones pinacolisation reaction by-products. The obtained results show that the complexes of the metals which present a high reducing and oxo-philic (Ti, Sm, U..) character react in a similar way with the carbonyl compounds. If the uranium compounds are less used than those of the titanium in the field of the organic synthesis applications, they are precious auxiliaries and excellent models for reactions mechanisms study and for the synthesis methods optimization. (O.M.)

  10. Dissolution of uranium oxide TBP-HNO3 complex

    International Nuclear Information System (INIS)

    Mizuno, Mineo; Kosaka, Yuji; Mori, Yukihide; Shimada, Takashi

    2002-12-01

    As a head end process for the pulverization of the spent fuel, the mechanical method (the shredder method) and the pyro-chemical method (oxidisation heat-treatment) have been examined. UO 2 is a main ingredient of Uranium oxide powder by the mechanical method, and U 3 O 8 is that by the pyro-chemical method. Moreover, the particle size of the pulverized powder depend on the conditions of the pulverizing process. As it was considered that the difference of dissolution rates of samples was caused by the difference of sample chemical forms and dissolution temperature, parametric surveys on chemical form and particle size of powder and dissolution temperature were carried out, and the following results were obtained. 1) The remarkable difference of dissolution rate between U 3 O 8 powder (average particle size 3.7 μm) and UO 2 powder (average particle size 2.4 μm) which have comparatively similar particle size was not observed. 2) It was confirmed that the dissolution rate became lower according to the particle size increase (average particle size 2.4 μm-1 mm). And it was considered that dissolution rate had strong dependency on particle size, according to the results that the powder with 1 mm particle size did not dissolute completely after 5 hours test. 3) The temperature dependency of the dissolution rate was confirmed by dissolution test with UO 2 powder (average particle size 2.4 μm-1 mm). The higher dissolution rate was obtained in the higher dissolution temperature, and 11 kcal/mol was obtained as activation energy of dissolution. 4) In the dissolution test of UO 2 powder, the nitric acid concentration started to change earlier than that of U 3 O 8 powder and concentration change range became larger compared with that in the dissolution test of U 3 O 8 powder. It was considered that those differences were caused by difference in mole ratio of Uranium and nitric acid which are consumed in the dissolution reaction (3:7 for U 3 O 8 , 3:8 for UO 2 ). 5) In case

  11. Syntheses and properties of complex resins obtained by the reaction of polyethyleneimine with maleic anhydride-isobutene copolymer

    International Nuclear Information System (INIS)

    Usami, Shiro; Hasegawa, Kiyoshi; Takata, Kyoko; Naito, Ryunosuke; Uchida, Hiroshi; Kozuka, Hiroshi.

    1985-01-01

    Complex resins obtained by the reaction of polyethyleneimine with maleic anhydride-isobutene copolymer around 100 0 C revealed selective ion adsorption depending on the equivalent ratio of nitrogen to carboxyl group (N/COOH). In detail, polyanion-excess complex resins (N/COOH 2+ , Pb 2+ , Zn 2+ and Ni 2+ , and resins containing excess polycation (N/COOH > 1) for metal complex anions such as [CrO 4 ] 2- , [Ag(S 2 O 3 ) 2 ] 3- and [Fe(CN) 6 ] 4- . Furthermore, the polycation-excess complex resins had high adsorption capacity for uranium in solution, for example, a polycationic resin (N/COOH = 1.79) had an adsorption capacity of more than 100 mg U/g-dry base resin in a 75 ppm uranium solution. It also adsorbed and recovered uranium from solution contatining such infinitesimal amounts of uranium as sea water. The results from electron probe X-ray microanalyser (EPMA) of a polycationic resin (N/COOH = 1.79) indicated that cations such as Ca 2+ and Mg 2+ , abundant in sea water, were not adsorbed at all while such anions as Cl - and S 2- were adsorbed. It was found that Br - , I - , etc. were not adsorbed from sea water while these anions were adsorbed from the solutions containing them independently. The result indicated that Cl - in sea water probably interfered the adsorption of Br - , I - , etc. However, uranium was adsorbed from sea water in spite of its extremely low concentration without any disturbance of other co-existing ions. It was found that Ni 2+ and Cu 2+ were also adsorbed. (author)

  12. Uranium

    International Nuclear Information System (INIS)

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

    1992-01-01

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

  13. Reactivity of uranium(IV) bridged chalcogenido complexes UIV–E–UIV (E = S, Se) with elemental sulfur and selenium: synthesis of polychalcogenido-bridged uranium complexes

    OpenAIRE

    Franke, Sebastian M.; Heinemann, Frank W.; Meyer, Karsten

    2014-01-01

    We report the syntheses, electronic properties, and molecular structures of a series of polychalcogenido-bridged dinuclear uranium species. These complexes are supported by the sterically encumbering but highly flexible, single N-anchored tris(aryloxide) chelator (AdArO)3N3−. Reaction of an appropriate uranium precursor, either the U(III) starting material, [((AdArO)3N)U(DME)], or the dinuclear mono-chalcogenido-bridged uranium(IV/IV) compounds [{((AdArO)3N)U(DME)}2(μ-E)] (E = S, Se), with el...

  14. The 1/4 technical scale, continuous process of obtaining the ceramic uranium dioxide from ammonium polyuranates containing fluoride

    International Nuclear Information System (INIS)

    Wlodarski, R.

    1977-01-01

    Based on the laboratory results, the 1/4 technical apparatus for the continuous reduction and defluorination of ammonium polyuranate containing fluoride was designed and constructed. The possibility of obtaining the ceramic uranium dioxide in a continuous process has been confirmed. The main part of the apparatus used in this process was the horizontal tubular oven with the extruder transporting material. (author)

  15. Uranium(iii) complexes supported by hydrobis(mercaptoimidazolyl)borates: synthesis and oxidation chemistry.

    Science.gov (United States)

    Maria, Leonor; Santos, Isabel C; Santos, Isabel

    2018-05-23

    The reaction of [UI3(thf)4] with the sodium or lithium salts of hydrobis(2-mercapto-1-methylimidazolyl)borate ligands ([H(R)B(timMe)2]-) in a 1 : 2 ratio, in tetrahydrofuran, gave the U(iii) complexes [UI{κ3-H,S,S'-H(R)B(timMe)2}2(thf)2] (R = H (1), Ph (2)) in good yields. Crystals of [UI{κ3-H,S,S'-H(Ph)B(timMe)2}2(thf)2] (2) were obtained by recrystallization from a tetrahydrofuran/acetonitrile solution, and the ion-separated uranium complex [U{κ3-H,S,S'-H(Ph)B(timMe)2}2(CH3CN)3][I] (3-I) was obtained by dissolution of 2 in acetonitrile followed by recrystallization. One-electron oxidation of 2 with AgBPh4 or I2 resulted in the formation of the cationic U(iv) complexes [U{κ3-H,S,S'-H(Ph)B(timMe)2}3][X] (X = BPh4 (6-BPh4), I (6-I)), due to a ligand redistribution process. These complexes are the first examples of homoleptic poly(azolyl)borate U(iv) complexes. Treatment of complex 2 with azobenzene led to the isolation of crystals of the U(iv) compound [UI{κ3-H(Ph)B(timMe)2}2(κ2-timMe)] (7). Treatment of 2 with pyridine-N oxide (pyNO) led to the formation of the uranyl complex [UO2{κ2-S,S'-H(Ph)B(timMe)2}2] (8) and of complex 6-I, while from the reaction of [U{κ3-H(Ph)B(timMe)2}2(thf)3][BPh4] (5) with pyNO, the oxo-bridged U(iv) complex [{U{κ3-H(Ph)B(timMe)2}2(pyNO)}2(μ-O)][BPh4]2 (9) was also obtained. In the U(iii) and U(iv) complexes, the bis(azolyl)borate ligands bind to the uranium center in a κ3-H,S,S' coordination mode, while in the U(vi) complex the ligands bind to the metal in a κ2-S,S' mode. The presence of UH-B interactions in the solid-state, for the nine-coordinate complexes 1, 2, 3, 6 and 7 and for the eight-coordinate complex 9, was supported by IR spectroscopy and/or X-ray diffraction analysis.

  16. Complex formation of uranium(VI) with fructose and glucose phosphates

    International Nuclear Information System (INIS)

    Koban, A.; Geipel, G.; Bernhard, G.; Fanghaenel, T.

    2002-01-01

    The uptake of heavy metals into plants is commonly quantified by the soil-plant transfer factor. Up to now little is known about the chemical speciation of actinides in plants. To compare the obtained spectroscopic data of uranium complexes in plants with model compounds, we investigate the complexation of uranium with relevant bioligands of various functionalities. A very important class of ligands consists of phosphate esters, which serve as phosphate group and energy transmitters as well as energy storage media in biological systems. Heavy metal ions bound to the phosphate esters can be transported into living cells and then deposited. Therefore, in our study we present the results of uranium complexation with glucose-6-phosphate (G6P), and fructose-6-phosphate (F6P) obtained by time-resolved laser-induced fluorescence spectroscopy (TRLFS). The experiments were performed at a fixed uranyl concentration (10 -5 M) as a function of the ligand concentrations (10 -5 to 10 -3 M) in a pH range from 2 to 4.5. For the glucose phosphate system we observed, using increasing ligand concentrations, a decrease in the fluorescence intensity and a small red shift of the emission bands. From this we conclude that the complexed uranyl glucose phosphate species show only minor or no fluorescence properties. The TRLFS spectra of the glucose phosphate samples indicated the presence of a single species with fluorescence properties. This species has a lifetime of approximately 1.5 μs and was identified as the free uranyl ion. An opposite phenomenon was observed for the fructose phosphate system: there was no decrease in fluorescence intensity. However, a strong red shift of the spectra was observed, illustrating the fluorescence properties of the uranyl fructose phosphate complex. The TRLFS spectra of the fructose phosphate system showed a second lifetime ( 2 2+ UO 2 (lig) x (2-y)+ + y H + (lig = sugar phosphate). Applying the mass action law and transformation to the logarithmic

  17. Trivalent metallocene chemistry of some uranium, titanium, and zirconium complexes

    International Nuclear Information System (INIS)

    Lukens, W.W. Jr.

    1995-05-01

    Dicyclopentadienyluranium halide dimers have been prepared and their solution behavior examined. These molecules exist as dimers in solution, and the halide ligands undergo rapid site exchange on the NMR timescale above 50 C. Analogous dicyclopentadienyluranium hydroxide dimers have also been prepared; they oxidatively eliminate hydrogen to give the corresponding oxide dimers. Mechanism of this reaction is consistent with αmigration of one of the hydroxide hydrogen atoms to a uranium center followed by elimination of hydrogen. Ground state of [(Me 3 Si) 2 C 5 H 3 ] 3 M M = Nd, U and their base adducts has been examined by variable temperature magnetic susceptibility and EPR spectroscopy. The ground state is found to be 4 I 9/2 with a crystal field state consisting largely of J z = 1/2 lowest, in agreement with previous studies on tris-cyclopentadienylneodymium complexes. The zirconium metallocene Cp 3 Zr has been prepared, characterized crystallographically, and its reactivity studied. Its chemical behavior is controlled by presence of an electron in the non-bonding, d z 2 orbital which prevents formation of base adducts Of Cp 3 Zr, but allows Cp 3 Zr to abstract atoms from other molecules. Electonic and EPR spectra of Cp* 2 TiX complexes, where Cp* is Me 5 C 5 and X is a monodentate, anionic ligand such as halide, have been studied. A π-bonding spectrochemical series is developed, and trends in π-bonding ability are found similar to those in other inorganic complexes. The β-agostic interactions in Cp* 2 TiN(Me)Ph have been examined using variable temperature EPR spectroscopy, and the enthalpy/entropy of the interaction determined. In Cp* 2 TiEt, enthalpy of the β-agostic interaction is -1.9 kcal/mol. The titanocene anion, Cp* 2 TiLi(TMEDA) (TMEDA is N,N,N',N'-tetramethylethylenediamine), has been prepared and its structure determined

  18. Single-molecule magnetism in a single-ion triamidoamine uranium(V) terminal mono-oxo complex

    International Nuclear Information System (INIS)

    King, David M.; McMaster, Jonathan; Lewis, William; Blake, Alexander J.; Liddle, Stephen T.; Tuna, Floriana; McInnes, Eric J.L.

    2013-01-01

    Straightforward oxidation of a triamidoamine uranium(III) complex with trimethyl-N-oxide affords a uranium(V) terminal mono-oxo complex which is the first clear-cut example of a uranium(V) single-molecule magnet (SMM). This monometallic complex unambiguously shows that a strongly axially ligated and thus anisotropic ligand field can be used to overcome the limited magnetic anisotropy of uranium(V). [de

  19. Uranium

    International Nuclear Information System (INIS)

    Anon.

    1984-01-01

    The article briefly discusses the Australian government policy and the attitude of political party factions towards the mining and exporting of the uranium resources in Australia. Australia has a third of the Western World's low-cost uranium resources

  20. Sorption of uranium (VI) on homoionic sodium smectite experimental study and surface complexation modeling.

    Science.gov (United States)

    Korichi, Smain; Bensmaili, Aicha

    2009-09-30

    This paper is an extension of a previous paper where the natural and purified clay in the homoionic Na form were physico-chemically characterized (doi:10.1016/j.clay.2008.04.014). In this study, the adsorption behavior of U (VI) on a purified Na-smectite suspension is studied using batch adsorption experiments and surface complexation modeling (double layer model). The sorption of uranium was investigated as a function of pH, uranium concentration, solid to liquid ratio, effect of natural organic matter (NOM) and NaNO(3) background electrolyte concentration. Using the MINTEQA2 program, the speciation of uranium was calculated as a function of pH and uranium concentration. Model predicted U (VI) aqueous speciation suggests that important aqueous species in the [U (VI)]=1mg/L and pH range 3-7 including UO(2)(2+), UO(2)OH(+), and (UO(2))(3)(OH)(5)(+). The concentration of UO(2)(2+) decreased and that of (UO(2))(3)(OH)(5)(+) increased with increasing pH. The potentiometric titration values and uptake of uranium in the sodium smectite suspension were simulated by FITEQL 4.0 program using a two sites model, which is composed of silicate and aluminum reaction sites. We compare the acidity constants values obtained by potentiometric titration from the purified sodium smectite with those obtained from single oxides (quartz and alpha-alumina), taking into account the surface heterogeneity and the complex nature of natural colloids. We investigate the uranium sorption onto purified Na-smectite assuming low, intermediate and high edge site surfaces which are estimated from specific surface area percentage. The sorption data is interpreted and modeled as a function of edge site surfaces. A relationship between uranium sorption and total site concentration was confirmed and explained through variation in estimated edge site surface value. The modeling study shows that, the convergence during DLM modeling is related to the best estimation of the edge site surface from the N(2

  1. Redox properties of biscyclopentadienyl uranium(V) imido-halide complexes: a relativistic DFT study.

    Science.gov (United States)

    Elkechai, Aziz; Kias, Farida; Talbi, Fazia; Boucekkine, Abdou

    2014-06-01

    Calculations of ionization energies (IE) and electron affinities (EA) of a series of biscyclopentadienyl imido-halide uranium(V) complexes Cp*2U(=N-2,6-(i)Pr2-C6H3)(X) with X =  F, Cl, Br, and I, related to the U(IV)/U(V) and U(V)/U(VI) redox systems, were carried out, for the first time, using density functional theory (DFT) in the framework of the relativistic zeroth order regular approximation (ZORA) coupled with the conductor-like screening model (COSMO) solvation approach. A very good linear correlation (R(2) =  0.993) was obtained, between calculated ionization energies at the ZORA/BP86/TZP level, and the experimental half-wave oxidation potentials E1/2. A similar linear correlation between the computed electron affinities and the electrochemical reduction U(IV)/U(III) potentials (R(2) =  0.996) is obtained. The importance of solvent effects and of spin-orbit coupling is definitively confirmed. The molecular orbital analysis underlines the crucial role played by the 5f orbitals of the central metal whereas the Nalewajski-Mrozek (N-M) bond indices explain well the bond distances variations following the redox processes. The IE variation of the complexes, i.e., IE(F) uranium charges and E1/2 in the reduction process of the U(V) species.

  2. Uranium

    International Nuclear Information System (INIS)

    Mackay, G.A.

    1978-01-01

    The author discusses the contribution made by various energy sources in the production of electricity. Estimates are made of the future nuclear contribution, the future demand for uranium and future sales of Australian uranium. Nuclear power growth in the United States, Japan and Western Europe is discussed. The present status of the six major Australian uranium deposits (Ranger, Jabiluka, Nabarlek, Koongarra, Yeelerrie and Beverley) is given. Australian legislation relevant to the uranium mining industry is also outlined

  3. Uranium

    International Nuclear Information System (INIS)

    1982-01-01

    The development, prospecting, research, processing and marketing of South Africa's uranium industry and the national policies surrounding this industry form the headlines of this work. The geology of South Africa's uranium occurences and their positions, the processes used in the extraction of South Africa's uranium and the utilisation of uranium for power production as represented by the Koeberg nuclear power station near Cape Town are included in this publication

  4. Uranium

    International Nuclear Information System (INIS)

    Stewart, E.D.J.

    1974-01-01

    A discussion is given of uranium as an energy source in The Australian economy. Figures and predictions are presented on the world supply-demand position and also figures are given on the added value that can be achieved by the processing of uranium. Conclusions are drawn about Australia's future policy with regard to uranium (R.L.)

  5. Uranium

    International Nuclear Information System (INIS)

    Toens, P.D.

    1981-03-01

    The geological setting of uranium resources in the world can be divided in two basic categories of resources and are defined as reasonably assured resources, estimated additional resources and speculative resources. Tables are given to illustrate these definitions. The increasing world production of uranium despite the cutback in the nuclear industry and the uranium requirements of the future concluded these lecture notes

  6. Catalytic properties and dynamic behaviour of uranium complexes

    International Nuclear Information System (INIS)

    Le Marechal, J.F.

    1986-01-01

    The catalytic properties of organometallic uranium III and IV compounds in solution as well as reaction mechanisms are studied. The structure in solution of CpUCl 3 L 2 (L=THF, HMPA, OPPh 3 , OP(OR) 3 ) is investigated. When L=HMPA, the complex exists in two isomers in equilibrium with the L ligands either in trans or mer-cis configuration. The isomerization (Ea=92 kJ mol -1 ) as well as the bimolecular exchange with an outer sphere ligand L are observable in 1 H and 31 P NMR, and quantified with the spin saturation transfer technique in several solvents and at different temperatures between 230 and 330 K. This property is extended to other ligands. The compound U(AlH 4 ) 3 is synthetized. This compound catalyses the hydroalumination of olefins by LiAlH 4 with a very good anti-Markovnikov regioselectivity. A simple mechanism for this reaction is suggested. The reactions of the organoaluminates products with several reactants (D 2 O, I 2 , CH 2 O, Allyl-Br...) has been shown to be a powerful synthetic tool. Some specific alkenes and alkynes exhibit an interesting behaviour as dimerization or β-alkyl elimination which is easily interpreted by our mechanism [fr

  7. Environmental Survey preliminary report, Portsmouth Uranium Enrichment Complex, Piketon, Ohio

    International Nuclear Information System (INIS)

    1987-08-01

    This report presents the preliminary findings from the first phase of the Environmental Survey of the United States Department of Energy (DOE) Portsmouth Uranium Enrichment Complex (PUEC), conducted August 4 through August 15, 1986. The Survey is being conducted by an interdisciplinary team of environmental specialists, led and managed by the Office of Environment, Safety and Health's Office of Environmental Audit. Team specialists are being supplied by a private contractor. The objective of the Survey is to identify environmental problems and areas of environmental regulation. It is being performed in accordance with the DOE Environmental Survey Manual. This phase of the Survey involves the review of existing site environmental data, observations of the operations performed at PUEC, and interviews with site personnel. The Survey team developed a Sampling and Analysis Plan to assist in further assessing certain of the environmental problems identified during its on-site activities. The Sampling and Analysis Plan will be executed by Argonne National Laboratory. When completed, the results will be incorporated into the PUEC Environmental Survey Interim Report. The Interim Report will reflect the final determinations of the PUEC Survey. 55 refs., 22 figs., 21 tabs

  8. Absorption spectra analysis of hydrated uranium(III) complex chlorides

    Science.gov (United States)

    Karbowiak, M.; Gajek, Z.; Drożdżyński, J.

    2000-11-01

    Absorption spectra of powdered samples of hydrated uranium(III) complex chlorides of the formulas NH 4UCl 4 · 4H 2O and CsUCl 4 · 3H 2O have been recorded at 4.2 K in the 4000-26 000 cm -1 range. The analysis of the spectra enabled the determination of crystal-field parameters and assignment of 83 and 77 crystal-field levels for the tetrahydrate and trihydrate, respectively. The energies of the levels were computed by applying a simplified angular overlap model as well as a semiempirical Hamiltonian representing the combined atomic and crystal-field interactions. Ab initio calculations have enabled the application of a simplified parameterization and the determination of the starting values of the AOM parameters. The received results have proved that the AOM approach can quite well predict both the structure of the ground multiplet and the positions of the crystal-field levels in the 17 000-25 000 cm -1 range, usually obscured by strong f-d bands.

  9. Synthesis and structure determination of a stable organometallic uranium(V) imine complex and its isolobal anionic U(IV)-ate complex

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, M.; Botoshanskii, M.; Eisen, M.S. [Schulich Faculty of Chemistry, and Institute of Catalysis Science and Technology, Technion Israel Institute of Technology, Haifa (Israel); Bannenberg, Th.; Tamm, M. [Institut fur Anorganische und Analytische Chemie, Technische Universitat Braunschweig (Germany)

    2010-06-15

    The reaction of one equivalent of Cp*{sub 2}UCl{sub 2} with 2-(trimethylsilyl-imino)-1,3-di-tert-butyl-imidazoline in boiling toluene afforded a one electron oxidation of the uranium metal and the opening of the N-heterocyclic ring, resulting in the formation of an organometallic uranium(V) imine complex. This complex crystallized with one molecule of toluene in the unit cell, and its solid-state structure was determined by X-ray diffraction analysis. When the same reaction was performed in perdeuterated toluene, a myriad of organometallic complexes were obtained, however, when equimolar amounts of water were used in toluene, the same complex was obtained, and its solid state characterization shows two independent molecules in the unit cell with an additional water molecule. For comparison of the geometric parameters, the corresponding isolobal anionic uranium(IV) complex [Cp*{sub 2}UCl{sub 3}]{sup -} was synthesized by the reaction of Cp*{sub 2}UCl{sub 2} with 1,3-di-tert-butyl-imidazolium chloride, and the resulting U(IV)-ate complex was characterized by X-ray diffraction analysis. (authors)

  10. EXAFS investigation of uranium(6) complexes formed at Acidithiobacillus ferro oxidans types

    International Nuclear Information System (INIS)

    Merroun, M.; Reich, T.; Hennig, Ch.; Selenska-Pobell, S.

    2002-01-01

    Mining activities have brought excessive amounts of uranium into the environment. In uranium deposits a number of acidophilic chemo-litho-autotrophic bacteria have been identified which are able to oxidize sulphide minerals, elemental sulphur, ferrous iron and also (in the presence of uranium mineral) U(IV). In particular, the interaction of one representative of the group Acidithiobacillus ferro oxidans (new designation of Thiobacillus ferro oxidans) with uranium has been investigated. Uranium(VI) complex formations at the surfaces of Acidithiobacillus ferro oxidans were studied using uranium L III -edge extended X-ray absorption fine structure (EXAFS) spectroscopy. In all samples uranium is co-ordinated by two axial oxygen atoms (O ax ) at a distance of 1.77-1.78 angstrom. The average distance between uranium and the equatorial oxygen atoms (O eq ) is 2.35 angstrom. The co-ordination number for O eq is 5-6. In comparison to the uranium crystal structure data, the U-O eq distance indicates a co-ordination number of the equatorial oxygen of 5. Within the experimental error, there are no differences in the U-O bond distances between samples from the three types of A. ferro oxidans investigated. The fit to the EXAFS data of samples measured as wet pastes gave the same results as for dried samples. No significant structural differences were observed for the uranium complexes formed by the eco-types of A. ferro oxidans. However, the EXAFS spectra do indicate a formation of uranium complexes which are different from those formed by Bacilli where the bond length of 2.28 angstrom indicates a co-ordination number of 4 for the equatorial oxygen atoms. (authors)

  11. Uranium hetero-bimetallic complexes: synthesis, structure and magnetic properties; Complexes heterobimetalliques de l'uranium: synthese, structure et proprietes magnetiques

    Energy Technology Data Exchange (ETDEWEB)

    Le Borgne, Th

    2000-10-04

    The aim of this thesis is to synthesize molecular complexes with uranium and transition metal ions in close proximity, to determine the nature of the magnetic interaction between them. We decided to use Schiff bases as assembling ligands, which are unusual for uranium (IV). Although the simplest Schiff bases, such as H{sub 2}Salen, lead to ligand exchange reactions, the bi-compartmental Schiff base H{sub 4}L{sup 6} (bis(3-hydroxy-salicylidene) - 2,2-dimethyl-propylene) allows the crystal structure determination of the complex [L{sup 6}Cu(pyr)]U[L{sup 6}Cu].2pyr, obtained by reaction of the metallo-ligand H{sub 2}L{sup 6}Cu with U(acac){sub 4}. In this manner, the complexes [L{sup 6}Co(pyr)]{sub 2}U and [L{sup 6}Ni(pyr)]{sub 2}U.pyr were also isolated, as well as the compounds in which the paramagnetic ions have been exchanged by the diamagnetic ions Zn{sup II}, Zr{sup IV} and Th{sup IV}': [L{sup 6}Zn(pyr)]{sub 2}U, [L{sup 6}Cu]{sub 2}Zr and [L{sup 6}Cu(pyr)]Th[L{sup 6}Cu].2pyr. These complexes are the first which involve three metallic centres assembling by the means of a hexa-dentate Schiff base. The crystalline structures show, for all these complexes, the outstanding orthogonal arrangement of the two fragments L{sup 6}M around the central atom which is in a dodecahedral environment of eight oxygen atoms of two Schiff bases. The syntheses of the isostructural complexes Cu2{sup II} and Zn{sub 2}U in which the uranium (IV) ion is close, in the first one, to the paramagnetic ion Cu{sup II} and, in the second one, to the diamagnetic ion Zn{sup II}, has allowed the use of the empiric method to determine the nature of the magnetic interaction between an f element and a transition metal. The comparison of the magnetic behaviour of two complexes Cu{sub 2}U and Zn{sub 2}U, expressed by the variation of {chi}T vs T, reveals the ferromagnetic interaction in the heart of the triad Cu-U-Cu. The magnetic behaviour of the complexes Cu{sub 2}Th et Cu{sub 2}Zr which does not

  12. Radium removal from Canadian uranium mining effluents by a radium-selective ion exchange complexer

    International Nuclear Information System (INIS)

    1984-07-01

    A laboratory test program was initiated by the Department of Energy, Mines and Resources as part of the National Uranium Tailings Program to investigate the applicability of a radium-selective ion exchange complexer for removing radium from Canadian uranium mining effluents. The ion exchange complexer was shown to be efficient in removing radium from contaminated water of uranium mining operations, with the ultimate loading capacity of the resin on one type of water treated being determined as approximately 1,600 Bq/cm 3 of new resin. The results showed that the resin was effective in removing radium but not any other contaminants

  13. Trivalent metallocene chemistry of some uranium, titanium, and zirconium complexes

    Energy Technology Data Exchange (ETDEWEB)

    Lukens, Jr., Wayne Wendell [Univ. of California, Berkeley, CA (United States)

    1995-05-01

    Dicyclopentadienyluranium halide dimers have been prepared and their solution behavior examined. These molecules exist as dimers in solution, and the halide ligands undergo rapid site exchange on the NMR timescale above 50 C. Analogous dicyclopentadienyluranium hydroxide dimers have also been prepared; they oxidatively eliminate hydrogen to give the corresponding oxide dimers. Mechanism of this reaction is consistent with αmigration of one of the hydroxide hydrogen atoms to a uranium center followed by elimination of hydrogen. Ground state of [(Me3Si)2C5H3]3M M = Nd, U and their base adducts has been examined by variable temperature magnetic susceptibility and EPR spectroscopy. The ground state is found to be 4I9/2 with a crystal field state consisting largely of Jz = 1/2 lowest, in agreement with previous studies on tris-cyclopentadienylneodymium complexes. The zirconium metallocene Cp3Zr has been prepared, characterized crystallographically, and its reactivity studied. Its chemical behavior is controlled by presence of an electron in the non-bonding, dz2 orbital which prevents formation of base adducts Of Cp3Zr, but allows Cp3Zr to abstract atoms from other molecules. Electonic and EPR spectra of Cp*2TiX complexes, where Cp* is Me5C5 and X is a monodentate, anionic ligand such as halide, have been studied. A π-bonding spectrochemical series is developed, and trends in π-bonding ability are found similar to those in other inorganic complexes. The β-agostic interactions in Cp*2TiN(Me)Ph have been examined using variable temperature EPR spectroscopy, and the enthalpy/entropy of the interaction determined. In Cp*2TiEt, enthalpy of the β-agostic interaction is -1.9 kcal/mol. The titanocene anion, Cp*2TiLi(TMEDA) (TMEDA is N,N,N`,N`-tetramethylethylenediamine), has been

  14. An oxyde mixture fuel containing uranium and plutonium dioxides and process to obtain this oxyde mixture

    International Nuclear Information System (INIS)

    Hannerz, K.

    1976-01-01

    An oxide-mixture fuel containing uranium and plutonium dioxides having the slage of spherical, or nearly spherical, oxide-mixture particles with a diameter within the range of from 0.2 to 2 mn charactarized in that each oxide-mixture particles is provided with an outer layer comprising mainly UO2, the thickness of which is at least 0.05; whereas the inner portion of the oxide-mixture particles comprises mainly PUO 2

  15. Evaluation of the uranium potential of the Bushveld Complex

    International Nuclear Information System (INIS)

    Cheney, E.S.

    1986-04-01

    The poor quality of the airborne radiometric surveys and the lack of exploration geochemical data in the public domain prevent a satisfactory assessment of the uranium potential of the Bushveld area. Undue reliance must be placed upon fitting models of uranium ore deposits to the geology of the Bushveld area. Although the Bushveld granites have an unusually high background of uranium (20 to 40 ppm), they probably only host small vein-type deposits. The vein at the Albert Silver mine should be investigated as a type example to determine if it is only economic in the narrow interval of supergene enrichment. The Rooiberg Group has considerable potential for caldera-related deposits and for uranium-bearing sulphide deposits (including Olympic Dam-type deposits) in sedimentary interbeds. The Loskop Formation appears to be correlative with the Glentig and lower Swaershoek Formations of the Waterberg area. The Waterberg Group is the logical host to investigate for giant uncomformity/vein-type uranium deposits like those in Canada and Australia. Because the Waterberg consists of four uncomformity-bounded sequences, it is rarely more than 3 km thick; all of the sequences could be younger than 1770 Ma

  16. Synthesis and insertion chemistry of mixed tether uranium metallocene complexes

    Energy Technology Data Exchange (ETDEWEB)

    Siladke, Nathan A.; LeDuc, Jennifer; Ziller, Joseph W.; Evans, William J. [Department of Chemistry, University of California, Irvine, CA (United States)

    2012-11-12

    The synthesis of mixed tethered alkyl uranium metallocenes has been investigated by examining the reactivity of the bis(tethered alkyl) metallocene [(η{sup 5}-C{sub 5}Me{sub 4}SiMe{sub 2}CH{sub 2}-κC){sub 2}U] (1) with substrates that react with only one of the U-C linkages. The effect of these mixed tether coordination environments on the reactivity of the remaining U-C bond has been studied by using CO insertion chemistry. One equivalent of azidoadamantane (AdN{sub 3}) reacts with 1 to yield the mixed tethered alkyl triazenido complex [(η{sup 5}-C{sub 5}Me{sub 4}SiMe{sub 2}CH{sub 2}-κC)U(η{sup 5}-C{sub 5}Me{sub 4}SiMe{sub 2}-CH{sub 2}NNN-Ad-κ{sup 2}N{sup 1,3})]. Similarly, a single equivalent of CS{sub 2} reacts with 1 to form the mixed tethered alkyl dithiocarboxylate complex [(η{sup 5}-C{sub 5}Me{sub 4}SiMe{sub 2}CH{sub 2}-κC)U(η{sup 5}-C{sub 5}Me{sub 4}SiMe{sub 2}- CH{sub 2}C(S){sub 2}-κ{sup 2}S,S{sup '})], a reaction that constitutes the first example of CS{sub 2} insertion into a U{sup 4+}-C bond. Complex 1 reacts with one equivalent of pyridine N-oxide by C-H bond activation of the pyridine ring to form a mixed tethered alkyl cyclometalated pyridine N-oxide complex [(η{sup 5}-C{sub 5}Me{sub 4}SiMe{sub 2}CH{sub 2}-κC)(η{sup 5}-C{sub 5}Me{sub 4}SiMe{sub 3})U(C{sub 6}H{sub 4}NO-κ{sup 2} C,O)]. The remaining (η{sup 5}-C{sub 5}Me{sub 4}SiMe{sub 2}CH{sub 2}-κC){sup 2-} ligand in each of these mixed tethered species show reactivity towards CO and tethered enolate ligands form by insertion. Subsequent rearrangement have been identified in [(η{sup 5}-C{sub 5}Me{sub 4}SiMe{sub 3})U(C{sub 5}H{sub 4}NO-κ{sup 2}C,O)(η{sup 5}-C{sub 5}Me{sub 4}SiMe{sub 2}C(=CH{sub 2})O- κO)] and [(η{sup 5}-C{sub 5}Me{sub 4}SiMe{sub 2}CH{sub 2}NNN-Ad-κ{sup 2}N{sup 1,3})U(η{sup 5}-C{sub 5}Me{sub 4}SiMe{sub 2}C(=CH{sub 2})O-κO)]. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  17. Oxo-group-14-element bond formation in binuclear uranium(V) pacman complexes

    International Nuclear Information System (INIS)

    Jones, Guy M.; Arnold, Polly L.; Love, Jason B.

    2013-01-01

    Simple and versatile routes to the functionalization of uranyl-derived U"V-oxo groups are presented. The oxo-lithiated, binuclear uranium(V)-oxo complexes [{(py)_3LiOUO}_2(L)] and [{(py)_3LiOUO}(OUOSiMe_3)(L)] were prepared by the direct combination of the uranyl(VI) silylamide ''ate'' complex [Li(py)_2][(OUO)(N'')_3](N''=N(SiMe_3)_2) with the polypyrrolic macrocycle H_4L or the mononuclear uranyl (VI) Pacman complex [UO_2(py)(H_2L)], respectively. These oxo-metalated complexes display distinct U-O single and multiple bonding patterns and an axial/equatorial arrangement of oxo ligands. Their ready availability allows the direct functionalization of the uranyl oxo group leading to the binuclear uranium(V) oxo-stannylated complexes [{(R_3Sn)OUO}_2(L)] (R=nBu, Ph), which represent rare examples of mixed uranium/tin complexes. Also, uranium-oxo-group exchange occurred in reactions with [TiCl(OiPr)_3] to form U-O-C bonds [{(py)_3LiOUO}(OUOiPr)(L)] and [(iPrOUO)_2(L)]. Overall, these represent the first family of uranium(V) complexes that are oxo-functionalised by Group 14 elements. (Copyright copyright 2013 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

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

    International Nuclear Information System (INIS)

    1995-05-01

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

  19. Uranium

    International Nuclear Information System (INIS)

    Whillans, R.T.

    1981-01-01

    Events in the Canadian uranium industry during 1980 are reviewed. Mine and mill expansions and exploration activity are described, as well as changes in governmental policy. Although demand for uranium is weak at the moment, the industry feels optimistic about the future. (LL)

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

    International Nuclear Information System (INIS)

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

    1958-01-01

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

  1. Bioreduction of Uranium(VI) Complexed with Citric Acid by Clostridia Affects its Structure and Mobility

    International Nuclear Information System (INIS)

    Francis, A.; Dodge, C.

    2008-01-01

    Uranium contamination of the environment from mining and milling operations, nuclear-waste disposal, and ammunition use is a widespread global problem. Natural attenuation processes such as bacterial reductive precipitation and immobilization of soluble uranium is gaining much attention. However, the presence of naturally occurring organic ligands can affect the precipitation of uranium. Here, we report that the anaerobic spore-forming bacteria Clostridia, ubiquitous in soils, sediments, and wastes, capable of reduction of Fe(III) to Fe(II), Mn(IV) to Mn(II), U(VI) to U(IV), Pu(IV) to Pu(III), and Tc(VI) to Tc(IV); reduced U(VI) associated with citric acid in a dinuclear 2:2 U(VI):citric acid complex to a biligand mononuclear 1:2 U(IV):citric acid complex, which remained in solution, in contrast to reduction and precipitation of uranium. Our findings show that U(VI) complexed with citric acid is readily accessible as an electron acceptor despite the inability of the bacterium to metabolize the complexed organic ligand. Furthermore, it suggests that the presence of organic ligands at uranium-contaminated sites can affect the mobility of the actinide under both oxic and anoxic conditions by forming such soluble complexes.

  2. Radiological risk assessment of U(nat) in the ground water around Jaduguda uranium mining complex

    International Nuclear Information System (INIS)

    Sethy, N.K.; Jha, V.N.; Shukla, A.K.; Tripathi, R.M.; Puranik, V.D.

    2010-01-01

    Uranium is present naturally in earth crust and hence at trace level in ground water, sea water, building materials etc. Naturally occurring radionuclide originating from industrial activities, metal mining and waste depository may contribute to the nearby ground water by radionuclide migration. Ground water ecosystem surrounding the uranium processing facility at Jaduguda has been studied for natural uranium distribution. In the present study, the drinking water sources at various distance zone (with in 1.6 km, 1.6-5 km and > 5km) covering all directions around the waste depository (tailings pond) have been investigated for uranium content. Evaluation of intake, ingestion dose and subsequent risk for population residing around the tailings pond has been carried out. Annual intake of uranium through drinking water for members of public residing around the uranium complex is found to be in the range of 41.8 - 44.4 Bq.y -1 . The intake and ingestion dose is appreciably low ( -1 ) which is far below the WHO recommended level of 100 Sv.y -1 . The life time radiological risk due to uranium natural in drinking water is insignificant and found to be of the order of 10 -6 . (author)

  3. Uranium

    Energy Technology Data Exchange (ETDEWEB)

    Williams, R M

    1976-01-01

    Evidence of expanding markets, improved prices and the short supply of uranium became abundantly clear in 1975, providing the much needed impetus for widespread activity in all phases of uranium operations. Exploration activity that had been at low levels in recent years in Canada was evident in most provinces as well as the Northwest Territories. All producers were in the process of expanding their uranium-producing facilities. Canada's Atomic Energy Control Board (AECB) by year-end had authorized the export of over 73,000 tons of U/sub 3/0/sub 8/ all since September 1974, when the federal government announced its new uranium export guidelines. World production, which had been in the order of 25,000 tons of U/sub 3/0/sub 8/ annually, was expected to reach about 28,000 tons in 1975, principally from increased output in the United States.

  4. Ligand Influences on Properties of Uranium Coordination Complexes - Structure, Reactivity, and Spectroscopy

    OpenAIRE

    Kosog, Boris

    2012-01-01

    In this thesis several different aspects of uranium chemistry are presented. It was shown that terminal uranium(V) oxo and imido complexes [((RArO)3tacn)UV(O)] and [((RArO)3tacn)UV(NSiMe3)] (R = t Bu, Ad) can be oxidized by silver(I) hexafluoro-antimonate to the uranium(VI) oxo and imido complexes [((RArO)3tacn)UVI(O)]SbF6 and [((RArO)3tacn)UVI(NSiMe3)]SbF6. While for the t Bu-derivative of the oxo complex an equatorial coordination is observed due to stabilization by the inverse trans-influe...

  5. Study of new complexes of uranium and comba radical. II-Complexes formed in the presence of OH-, CO3H, CH3-COO-, and B4O7

    International Nuclear Information System (INIS)

    Vera Palomino, V.; Galiano Sedano, J. A.; Parellada Bellod, R.; Bellido Gonzalez, A.

    1975-01-01

    Several complexes extracted with CDMBAC organic solutions from uranium aqueous solutions, in presence of sodium and ammonium hydroxides, are studied. These complexes fit to the general formula: U0 2 (OH) n (C[DMBA) n -2 . The uranium extraction in presence of an excess of sodium bicarbonate is also studied. From aqueous solutions of uranyl acetate we have isolated the complex U0 2 (CH 3 -C00) n (CDMBA) n -2. In presence of boric acid and sodium tetraborate an U-CDMBA compound containing boron in its molecule has being obtained by precipitation and liquid-liquid extraction. (Author) 5 refs

  6. Single-molecule magnetism in a single-ion triamidoamine uranium(V) terminal mono-oxo complex

    Energy Technology Data Exchange (ETDEWEB)

    King, David M.; McMaster, Jonathan; Lewis, William; Blake, Alexander J.; Liddle, Stephen T. [School of Chemistry, University of Nottingham (United Kingdom); Tuna, Floriana; McInnes, Eric J.L. [School of Chemistry and Photon Science Institute, University of Manchester (United Kingdom)

    2013-04-26

    Straightforward oxidation of a triamidoamine uranium(III) complex with trimethyl-N-oxide affords a uranium(V) terminal mono-oxo complex which is the first clear-cut example of a uranium(V) single-molecule magnet (SMM). This monometallic complex unambiguously shows that a strongly axially ligated and thus anisotropic ligand field can be used to overcome the limited magnetic anisotropy of uranium(V). (Copyright copyright 2013 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  7. Single-molecule magnetism in a single-ion triamidoamine uranium(V) terminal mono-oxo complex

    International Nuclear Information System (INIS)

    King, David M.; McMaster, Jonathan; Lewis, William; Blake, Alexander J.; Liddle, Stephen T.; Tuna, Floriana; McInnes, Eric J.L.

    2013-01-01

    Straightforward oxidation of a triamidoamine uranium(III) complex with trimethyl-N-oxide affords a uranium(V) terminal mono-oxo complex which is the first clear-cut example of a uranium(V) single-molecule magnet (SMM). This monometallic complex unambiguously shows that a strongly axially ligated and thus anisotropic ligand field can be used to overcome the limited magnetic anisotropy of uranium(V). (Copyright copyright 2013 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  8. Ultraviolet-B radiation mobilizes uranium from uranium-dissolved organic carbon complexes in aquatic systems, demonstrated by asymmetrical flow field-flow fractionation.

    Science.gov (United States)

    Nehete, Sachin Vilas; Christensen, Terje; Salbu, Brit; Teien, Hans-Christian

    2017-05-05

    Humic substances have a tendency to form complexes with metal ions in aquatic medium, impacting the metal mobility, decreasing bioavailability and toxicity. Ultraviolet-B (UV-B) radiation exposure degrades the humic substance, changes their molecular weight distribution and their metal binding capacity in aquatic medium. In this study, we experimented the effect of UV-B radiation on the uranium complexed with fulvic acids and humic acids in a soft water system at different pH, uranium concentrations and radiant exposure. The concentration and distribution of uranium in a complexed form were investigated by asymmetrical flow field-flow fractionation coupled to multi detection technique (AsFlFFF-UV-ICP-MS). The major concentration of uranium present in complexes was primarily associated with average and higher molecular weight fulvic and humic acids components. The concentration of uranium in a complexed form increased with increasing fulvic and humic acid concentrations as well as pH of the solution. The higher molecular weight fraction of uranium was degraded due to the UV-B exposure, transforming about 50% of the uranium-dissolved organic carbon complexes into low molecular weight uranium species in complex form with organic ligands and/or free form. The result also suggests AsFlFFF-UV-ICP-MS to be an important separation and detection technique for understanding the interaction of radionuclides with dissolved organic matter, tracking size distribution changes during degradation of organic complexes for understanding mobility, bioavailability and ecosystem transfer of radionuclides as well as metals. Copyright © 2017 Elsevier B.V. All rights reserved.

  9. Uranium

    International Nuclear Information System (INIS)

    Perkin, D.J.

    1982-01-01

    Developments in the Australian uranium industry during 1980 are reviewed. Mine production increased markedly to 1841 t U 3 O 8 because of output from the new concentrator at Nabarlek and 1131 t of U 3 O 8 were exported at a nominal value of $37.19/lb. Several new contracts were signed for the sale of yellowcake from Ranger and Nabarlek Mines. Other developments include the decision by the joint venturers in the Olympic Dam Project to sink an exploration shaft and the release of an environmental impact statement for the Honeymoon deposit. Uranium exploration expenditure increased in 1980 and additions were made to Australia's demonstrated economic uranium resources. A world review is included

  10. Uranium

    International Nuclear Information System (INIS)

    Gabelman, J.W.; Chenoweth, W.L.; Ingerson, E.

    1981-01-01

    The uranium production industry is well into its third recession during the nuclear era (since 1945). Exploration is drastically curtailed, and many staffs are being reduced. Historical market price production trends are discussed. A total of 3.07 million acres of land was acquired for exploration; drastic decrease. Surface drilling footage was reduced sharply; an estimated 250 drill rigs were used by the uranium industry during 1980. Land acquisition costs increased 8%. The domestic reserve changes are detailed by cause: exploration, re-evaluation, or production. Two significant discoveries of deposits were made in Mohave County, Arizona. Uranium production during 1980 was 21,850 short tons U 3 O 8 ; an increase of 17% from 1979. Domestic and foreign exploration highlights were given. Major producing areas for the US are San Juan basin, Wyoming basins, Texas coastal plain, Paradox basin, northeastern Washington, Henry Mountains, Utah, central Colorado, and the McDermitt caldera in Nevada and Oregon. 3 figures, 8 tables

  11. Environmental significance of copper, lead, manganese, uranium and zinc speciation in the event of contaminated waters release from the Ranger Uranium Mining Complex

    International Nuclear Information System (INIS)

    Noller, B.N.; Currey, N.A.

    1983-01-01

    The likely impact of the accidental release of tailings dam water during the dry season at the Ranger Uranium Mining Complex was examined. A speciation scheme utilising sizing by filtration and ion-exchange with Chelex 100 has given an insight into the likely partitioning of zinc, copper, lead, manganese and uranium following the addition of tailings dam water to samples from waterbodies in the vicinity of the uranium mining/milling complex. The speciation findings are discussed in terms of likely toxic effects on fish

  12. Interest of uranium complexes for the mechanism study of the McMurry reaction; Interet des complexes de l`uranium pour l`etude du mecanisme de la reaction de McMurry

    Energy Technology Data Exchange (ETDEWEB)

    Maury, O

    1997-07-04

    The reducing coupling reactions of ketones in diols and olefins are generally carried out with titanium or samarium compounds. In this work uranium complexes have been used. They have allowed to study the chemical reaction mechanism. This thesis is divided into three parts: 1) the reduction mechanism of uranium tetrachloride by cyclic voltametry has been studied at first. It has been shown that this reduction is followed by a transfer reaction of chlorides between the reduced specie of the higher electronic density and UCl . 2) In the second part is described: the synthesis, the crystal structure, the reactivity of the chemical agents, the stereochemistry of diols and alkenes formation and the pinacolisation reaction catalysis. 3) In the last part, the limits of the McMurry reaction are given by the study of the aromatic ketones pinacolisation reaction by-products. The obtained results show that the complexes of the metals which present a high reducing and oxo-philic (Ti, Sm, U..) character react in a similar way with the carbonyl compounds. If the uranium compounds are less used than those of the titanium in the field of the organic synthesis applications, they are precious auxiliaries and excellent models for reactions mechanisms study and for the synthesis methods optimization. (O.M.). 284 refs.

  13. The Y-12 National Security Complex Foreign Research Reactor Uranium Supply Production

    Energy Technology Data Exchange (ETDEWEB)

    Nelson, T. [Nuclear Technology and Nonproliferation Programs, B and W Y-12, L.L.C., Y-12 National Security Complex, Oak Ridge, Tennessee (United States); Keller, A.P. [Disposition and Supply Programs, B and W Y-12, L.L.C., Y-12 National Security Complex, Oak Ridge, Tennessee (United States)

    2011-07-01

    The Foreign Research Reactor (FRR) Uranium Supply Program at the Y-12 National Security Complex supports the nonproliferation objectives of the National Nuclear Security Administration (NNSA) HEU Disposition, the Reduced Enrichment Research and Test Reactors (RERTR), and the United States (U.S.) FRR Spent Nuclear Fuel (SNF) Acceptance Programs. The FRR Supply Program supports the important U.S. government nuclear nonproliferation commitment to serve as a reliable and cost-effective uranium supplier for those foreign research reactors that are converting or have converted to Low-Enriched Uranium (LEU) fuel under the RERTR Program. The NNSA Y-12 Site Office maintains the prime contracts with foreign government agencies for the supply of LEU for their research reactors. The LEU is produced by down blending Highly Enriched Uranium (HEU) that has been declared surplus to the U.S. national defense needs. The down blending and sale of the LEU supports the Surplus HEU Disposition Program Record of Decision to make the HEU non-weapons usable and to recover the economic value of the uranium to the extent feasible. In addition to uranium metal feedstock for fuel fabrication, Y-12 can produce LEU in different forms to support new fuel development or target fabrication for medical isotope production. With production improvements and efficient delivery preparations, Y-12 continues to successfully support the global research reactor community. (author)

  14. Study of aqueous complexes of uranium (IV) in an acid medium by nuclear magnetic resonance

    International Nuclear Information System (INIS)

    Kiener, C.; Folcher, G.; Rigny, P.; Virlet, J.

    1976-01-01

    The hydration of tetravalent uranium in acid solutions has been studied by proton magnetic resonance. Longitudinal and transversal relaxation rates of water are reported as a function of temperature, acidity, and added ions. The relaxation rates observed in perchloric solutions at high temperature are governed by the exchange process of water molecules between the inner coordination sphere of uranium(IV) and the bulk water. The bound proton's lifetime lies between 10 ms and 1 s. At pH > 0, the exchange rate depends upon acidity according to a simple expression. At high concentrations of diamagnetic ions the exchange rate depends linearly upon water activity. At low temperature, the proton relaxation rates are dominated by an outer sphere effect and the electronic relaxation time of uranium(IV) is found to be about 10 -13 s. No signal is observed from protons of the water molecules in the first sphere, firmly bound to uranium(IV), which undergo rapid relaxation. The chemical shift of the proton absorption signal in hydrochloric solutions arise from tightly bound water molecules in paramagnetic interaction with uranium(IV) in a second sphere, and in fast exchange with the bulk water. Above a chlorine concentration of 6 M, the monochloro complex of uranium(IV) contributes to the chemical shift. (author)

  15. Oxo-group-14-element bond formation in binuclear uranium(V) pacman complexes

    Energy Technology Data Exchange (ETDEWEB)

    Jones, Guy M.; Arnold, Polly L.; Love, Jason B. [EaStCHEM School of Chemistry, University of Edinburgh (United Kingdom)

    2013-07-29

    Simple and versatile routes to the functionalization of uranyl-derived U{sup V}-oxo groups are presented. The oxo-lithiated, binuclear uranium(V)-oxo complexes [{(py)_3LiOUO}{sub 2}(L)] and [{(py)_3LiOUO}(OUOSiMe{sub 3})(L)] were prepared by the direct combination of the uranyl(VI) silylamide ''ate'' complex [Li(py){sub 2}][(OUO)(N''){sub 3}](N''=N(SiMe{sub 3}){sub 2}) with the polypyrrolic macrocycle H{sub 4}L or the mononuclear uranyl (VI) Pacman complex [UO{sub 2}(py)(H{sub 2}L)], respectively. These oxo-metalated complexes display distinct U-O single and multiple bonding patterns and an axial/equatorial arrangement of oxo ligands. Their ready availability allows the direct functionalization of the uranyl oxo group leading to the binuclear uranium(V) oxo-stannylated complexes [{(R_3Sn)OUO}{sub 2}(L)] (R=nBu, Ph), which represent rare examples of mixed uranium/tin complexes. Also, uranium-oxo-group exchange occurred in reactions with [TiCl(OiPr){sub 3}] to form U-O-C bonds [{(py)_3LiOUO}(OUOiPr)(L)] and [(iPrOUO){sub 2}(L)]. Overall, these represent the first family of uranium(V) complexes that are oxo-functionalised by Group 14 elements. (Copyright copyright 2013 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  16. Uranium

    International Nuclear Information System (INIS)

    Anon.

    1983-01-01

    Recent decisions by the Australian Government will ensure a significant expansion of the uranium industry. Development at Roxby Downs may proceed and Ranger may fulfil two new contracts but the decision specifies that apart from Roxby Downs, no new mines should be approved. The ACTU maintains an anti-uranium policy but reaction to the decision from the trade union movement has been muted. The Australian Science and Technology Council (ASTEC) has been asked by the Government to conduct an inquiry into a number of issues relating to Australia's role in the nuclear fuel cycle. The inquiry will examine in particular Australia's nuclear safeguards arrangements and the adequacy of existing waste management technology. In two additional decisions the Government has dissociated itself from a study into the feasibility of establishing an enrichment operation and has abolished the Uranium Advisory Council. Although Australian reserves account for 20% of the total in the Western World, Australia accounts for a relatively minor proportion of the world's uranium production

  17. Uranium

    International Nuclear Information System (INIS)

    Anon.

    1981-01-01

    The French Government has decided to freeze a substantial part of its nuclear power programme. Work has been halted on 18 reactors. This power programme is discussed, as well as the effect it has on the supply of uranium by South Africa

  18. Diazoalkane reduction for the synthesis of uranium hydrazonido complexes

    Energy Technology Data Exchange (ETDEWEB)

    Matson, Ellen M.; Fanwick, Phillip E.; Bart, Suzanne C. [Department of Chemistry, Purdue University, West Lafayette, IN (United States)

    2012-11-15

    The reactivity of the uranium(III) alkyl Tp*{sub 2}UCH{sub 2}Ph (1) toward diazoalkanes is reported. Addition of 1 equiv. N{sub 2}CPh{sub 2} produces 0.5 equiv. bibenzyl, along with Tp*{sub 2}U(N{sub 2}CPh{sub 2}) (2). This species is dynamic in solution at room temperature and rapidly interconverts between the η{sup 1}- and η{sup 2} isomers as determined by variable-temperature {sup 1}H NMR spectroscopy. X-ray crystallographic analysis at low temperature shows exclusively the η{sup 2} isomer, which features a short U-N multiple bond analogous to an imido species. The η{sup 1} isomer reacts quantitatively with aldehydes and ketones through multiple bond metathesis to produce Tp*{sub 2}U(O) and the corresponding ketazine. Treatment of 1 with N{sub 2}CHSiMe{sub 3} generates 0.5 equiv. bibenzyl and the η{sup 1} isomer Tp*{sub 2}U(N{sub 2}CHSiMe{sub 3}) (3). This species is unstable over the course of hours, and there is no spectroscopic evidence for the η{sup 2} isomer. Tp*{sub 2}U(η{sup 1}-N{sub 2}CHSiMe{sub 3}) can be trapped by addition of phenylacetylene by a [2+2] cycloaddition to afford the uranium(IV) metallacycle Tp*{sub 2}U[(N-N = CHSiMe{sub 3})CHCPh] (4). Crystallographic data for 4 are presented. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  19. Thermochemistry of the complex oxides of uranium, vanadium, and alkali metals

    International Nuclear Information System (INIS)

    Karyakin, N.V.; Chernorukov, N.G.; Suleimanov, E.V.; Kharyushina, E.A.

    1992-01-01

    The standard enthalpies of the formation at T 298.15 K of complex oxides of uranium(VI), vanadium(V) and alkali metals with the general formula M 1 VUO 6 where M 1 = Na, K, Rb, and Cs, were calculated from the results of calorimetric experiments and from published data. 8 refs., 1 tab

  20. Surface complexation models for uranium adsorption in the sub-surface environment

    International Nuclear Information System (INIS)

    Payne, T.E.

    2007-01-01

    Adsorption experiments with soil component minerals under a range of conditions are being used to develop models of uranium(VI) uptake in the sub-surface environment. The results show that adsorption of U on iron oxides and clay minerals is influenced by chemical factors including the pH, partial pressure of CO 2 , and the presence of ligands such as phosphate. Surface complexation models (SCMs) can be used to simulate U adsorption on these minerals. The SCMs are based on plausible mechanistic assumptions and describe the experimental data more adequately than Kd values or sorption isotherms. It is conceptually possible to simulate U sorption data on complex natural samples by combining SCMs for individual component minerals. This approach was used to develop a SCM for U adsorption to mineral assemblages from Koongarra (Australia), and produced a reasonable description of U uptake. In order to assess the applicability of experimental data to the field situation, in-situ measurements of U distributions between solid and liquid phases were undertaken at the Koongarra U deposit. This field partitioning data showed a satisfactory agreement with laboratory sorption data obtained under comparable conditions. (author)

  1. Public communication on times of environmental crisis. The opening of San Rafael 's uranium complex

    International Nuclear Information System (INIS)

    Calvino, Carlos; Cisneros, Martin

    2008-01-01

    Full text: Argentina has had a lot of cultural changes in the last few years. An environmental movement has gathered and is trying to stop the opening of the Sierra Pintada uranium complex, near the city of San Rafael, in the south of Mendoza province. Since 2005, several 'groundless information' have been published in the local media about the dangers of this re-opening. These news exaggerate the properties of radon gas, claiming that it will reach San Rafael city (20 miles from the complex), rising radiological risk among the population, etc. This scene shows a 'non-real' picture of the regulatory activities that the Nuclear Regulatory Authority (ARN), a government agency that regulates nuclear facilities in Argentina, is really and systematically accomplishing. In this situation, the board of Directors of ARN decided to entrust a full analysis of the environmental issue in the area. The Office of Press and Communication implemented a local communication plan, using a Strategic and Systemic tool kit. The period to be analyzed is from second semester 2005 to February 2007. A little bit of history: the San Rafael Complex started in September 20 of 1979. It belongs to the National Commission of Atomic Energy (CNEA), a government agency. Until its temporary suspension in 1995 for international market reasons (uranium price was U$S 10 / pound), almost 2 million tons of uranium were processed. Besides its temporary suspension, the ARN has been constantly monitoring this particular former complex. In the year 2001, CNEA notices that the uranium price starts to rise and entrust National Technology University, Avellaneda Branch, to accomplish an Environmental Impact Report, according to the argentine law 25.585. Due especially to the rising of uranium price, (actually, the uranium price is approximately U$S 200) the national government determined to restart the extraction of the mineral again. By the year 2004, with the results of the Environmental Impact report, CNEA

  2. Spectroscopic Confirmation of Uranium (VI)-Carbonato Adsorption Complexes on Hematite

    International Nuclear Information System (INIS)

    Bargar, John R

    1999-01-01

    Evaluating societal risks posed by uranium contamination from waste management facilities, mining sites, and heavy industry requires knowledge about uranium transport in groundwater, often the most significant pathway of exposure to humans. It has been proposed that uranium mobility in aquifers may be controlled by adsorption of U(VI)-carbonato complexes on oxide minerals. The existence of such complexes has not been demonstrated, and little is known about their compositions and reaction stoichiometries. We have used Attenuated Total Reflectance Fourier Transform Infrared (ATR-FTIR) and Extended X-ray Absorption Fine Structure (EXAFS) spectroscopies to probe the existence, structures, and compositions of FeO surface -U(VI)-carbonato complexes on hematite throughout the pH range of uranyl uptake under conditions relevant to aquifers. U(VI)-carbonato complexes were found to be the predominant adsorbed U(VI) species at all pH values examined, a much wider pH range than previously postulated based on analogy to aqueous U(VI)-carbonato complexes, which are trace constituents at pH < 6. This result indicates the inadequacy of the common modeling assumption that the compositions and predominance of adsorbed species can be inferred from aqueous species. By extension, adsorbed carbonato complexes may be of major importance to the groundwater transport of similar actinide contaminants such as neptunium and plutonium

  3. Spectroscopic confirmation of uranium(VI)-carbonato adsorption complexes on hematite

    Science.gov (United States)

    Bargar, John R.; Reitmeyer, Rebecca; Davis, James A.

    1999-01-01

    Evaluating societal risks posed by uranium contamination from waste management facilities, mining sites, and heavy industry requires knowledge about uranium transport in groundwater, often the most significant pathway of exposure to humans. It has been proposed that uranium mobility in aquifers may be controlled by adsorption of U(VI)−carbonato complexes on oxide minerals. The existence of such complexes has not been demonstrated, and little is known about their compositions and reaction stoichiometries. We have used attenuated total reflectance Fourier transform infrared (ATR-FTIR) and extended X-ray absorption fine structure (EXAFS) spectroscopies to probe the existence, structures, and compositions of ≡FeOsurface−U(VI)−carbonato complexes on hematite throughout the pH range of uranyl uptake under conditions relevant to aquifers. U(VI)−carbonato complexes were found to be the predominant adsorbed U(VI) species at all pH values examined, a much wider pH range than previously postulated based on analogy to aqueous U(VI)−carbonato complexes, which are trace constituents at pH carbonato complexes may be of major importance to the groundwater transport of similar actinide contaminants such as neptunium and plutonium.

  4. Distribution of radium and chemical toxins in the environment of a uranium complex

    International Nuclear Information System (INIS)

    Markose, P.M.; Eapen, K.P.; Venkataraman, S.; Kamath, P.R.

    1978-01-01

    The discharge of waste effluents from mining and milling of uranium ore brings into the aquatic environment radioactive pollutants and chemical toxins. The radioactive element of primary concern is radium and the nonactive pollutants are manganese, chlorides, sulphates and water hardness. In the Uranium Complex, Bihar (India), the low grade ore is mined and processed for recovery of uranium. The waste slurries from the process are neutralised and discharged into the tailings pond(TP) where the solids settle and the effluents flow out into a natural stream, Jurianala. The TP effluent mixes with mine water and floor washings from the mill in the canal on its down stream course to the river, R. Subarnarekha. This study was conducted to assess the total pollution from the liquid discharges in the environment and the impact of discharge on water quality. The results of the study of movement of pollutants in the biosphere and laboratory investigations on containment are presented. (author)

  5. Extraction of uranium from sea water by means of fibrous complex adsorbents

    International Nuclear Information System (INIS)

    Miyamatsu, Tokuhisa; Oguchi, Noboru; Kanchiku, Yoshihiko; Aoyagi, Takanobu

    1982-01-01

    Fibrous complex adsorbents for uranium extraction from sea water were prepared by introducing titanic acid or basic zinc carbonate as effective constituents into fibrous ion exchangers. A fibrous chelate type adsorbent was also tested. Among the adsorbents examined, the following ones demonstrated excellent properties for the recovery of uranium from sea water. a) A fibrous, weakly acidic cation exchanger was treated with titanyl sulfate in aqueous sulfuric acid solution, which was followed by neutralization to afford a fibrous adsorbent containing titanic acid (QC-1f(Ti)). The adsorption capacity for uranium in sea water was estimated by extrapolation to be 50μg-U/g-Ad or 1170 μg-U/g-Ti. b) A fibrous, strongly acidic cation exchanger was treated in a similar way to afford another type of fibrous adsorbent with titanic acid incorporated (QCS-Ti). The adsorption capacity was estimated by extrapolation to be 20-30 μg-U/g-Ad. (author)

  6. Magnetic-superexchange interactions of uranium(IV) chloride-addition complexes with amides, 2

    International Nuclear Information System (INIS)

    Miyake, Chie; Hinatsu, Yukio; Imoto, Shosuke

    1983-01-01

    The magnetic susceptibilities of five cyclic amide (lactam)-addition complexes of uranium(IV) chloride were measured between room temperature and 2 K. Magnetic-exchange interaction was found only for N-methyl-substituted amide complexes, and a dimer structure was assumed for them on the basis of their chemical properties. Treating interdimer interaction with a molecular-field approximation, the magnetic susceptibilities were calculated to be in good agreement with the experimental results in the temperature region of the maxima in chi sub(A). The transmission of antiparallel spin coupling via the π orbitals of the bridging amide ligands is proposed to explain the strong intradimer superexchange interaction for the uranium(IV) chloride-amide complexes with the magnetic-susceptibility maximum. (author)

  7. Uranium-lead age determinations on granitic rocks from the eastern Bushveld Complex

    International Nuclear Information System (INIS)

    Faurie, J.N.

    1978-08-01

    Uranium-lead age determinations were carried out on four types of granitic rocks from the eastern Bushveld Complex. The oldest rocks in the area are gneisses and felsites - 2604 plus minus 100 m.y. old - which form the centre of the Dennilton dome. The Rooiberg felsites could not be dated directly because of the absence of zircon, however a porphyritic granite sill, which shows intrusive relations with the Rooiberg felsites, was dated at 2090 plus minus 40 m.y., an age which can also be regarded as a minimum age for the Rooiberg felsites. No reliable age could be determined for the granophyres because of the large amount of lead-loss reflected in the zircon. The majority of zircons from these granophyres showed a peculiar hieroglyphic texture, a phenomena which has not yet been recorded in literature. The samples collected from the granites gave an age of 1950 plus minus 80 m.y. and thus form part of the Nebo Granite. Attempts have been made to obtain more concordant zircon ages throughout the present study. Although some success was achieved by analysing different size fractions of a zircon population, the non-magnetic fractions gave the most promising results [af

  8. Foreign research reactor uranium supply program: The Y-12 national security complex process

    International Nuclear Information System (INIS)

    Nelson, T.; Eddy, B.G.

    2010-01-01

    The Foreign Research Reactor (FRR) Uranium Supply Program at the Y-12 National Security Complex supports the nonproliferation objectives of the HEU Disposition Program, the Reduced Enrichment Research and Test Reactors (RERTR) Program, and the United States FRR Spent Nuclear Fuel (SNF) Acceptance Program. The Y-12 National Nuclear Security Administration (NNSA) Y-12 Site Office maintains the prime contracts with foreign governments for the supply of Low-Enriched Uranium (LEU) for their research reactors. The LEU is produced by down blending Highly Enriched Uranium (HEU) that has been declared surplus to the U.S. national defense needs. The down blending and sale of the LEU supports the Surplus HEU Disposition Program Record of Decision to make the HEU non-weapons usable and to recover the economic value of the uranium to the extent feasible. This program supports the important U.S. government and nuclear nonproliferation commitment to serve as a reliable and cost-effective uranium supplier for those foreign research reactors that are converting or have converted to LEU fuel under the guidance of the NNSA RERTR Program. In conjunction with the FRR SNF Acceptance Program which supports the global nonproliferation efforts to disposition U.S.-origin HEU, the Y-12 FRR Uranium Supply Program can provide the LEU for the replacement fuel fabrication. In addition to feedstock for fuel fabrication, Y-12 supplies LEU for target fabrication for medical isotope production. The Y-12 process uses supply forecasting tools, production improvements and efficient delivery preparations to successfully support the global research reactor community

  9. Magnetic study of solid uranium-fluorine complexes; Contribution a l'etude magnetique de composes fluores solides de l'uranium

    Energy Technology Data Exchange (ETDEWEB)

    Dianoux, A J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1969-06-01

    A study of the magnetic susceptibility of uranium V fluorine complexes and of the magnetic resonance of fluorine atoms in uranium VI fluorine complexes has made it possible to put forward a structural model for these compounds for which it is impossible, because of the lack of suitable single crystals for X-ray diffraction work, to deduce the exact position of the fluorine atoms. It is shown that it is difficult to interpret the paramagnetism of uranium fluorides, because the uranium ions are in low-symmetry sites. A theoretical study of the magnetism of the U{sup V} ion in complex fluorides of the type M{sub 3}UF{sub 8} (M = NH{sub 4}, Na, Rb, Cs) leads to an interpretation based on a trigonal deformation of the eight fluorine atom structure surrounding the uranium atom. By applying a Hamiltonian spin formalism and making a systematic use of group theory, it is possible to present the susceptibility calculations very concisely. Study of the resonance and of the relaxation of the fluorine atoms in powdered uranium VI complex fluorides suggests a structural model in the case of NaUF{sub 7}. It is shown that the shape of the magnetic resonance absorption lines is strongly affected by the presence of large anisotropic chemical shifts. In the model proposed here, six fluorine atoms are linked to the uranium, atom by strongly covalent bonds in a deformed UF{sub 6} octahedral structure; the seventh fluorine atom remains ionic. The occurrence of a rotational movement of the octahedron is confirmed by a study of the longitudinal relaxation of the fluorine atoms, the activation energy being 0.46 eV. (author) [French] L'etude de la susceptibilite magnetique de complexes fluores d'uranium V et la resonance magnetique des fluors dans des complexes fluores d'uranium VI permettent de proposer un modele structural pour ces composes, ou la diffraction des rayons X, en l'absence de monocristaux convenables, est incapable de preciser la position des atomes de fluor. Nous montrons

  10. Magnetic study of solid uranium-fluorine complexes; Contribution a l'etude magnetique de composes fluores solides de l'uranium

    Energy Technology Data Exchange (ETDEWEB)

    Dianoux, A.J. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1969-06-01

    A study of the magnetic susceptibility of uranium V fluorine complexes and of the magnetic resonance of fluorine atoms in uranium VI fluorine complexes has made it possible to put forward a structural model for these compounds for which it is impossible, because of the lack of suitable single crystals for X-ray diffraction work, to deduce the exact position of the fluorine atoms. It is shown that it is difficult to interpret the paramagnetism of uranium fluorides, because the uranium ions are in low-symmetry sites. A theoretical study of the magnetism of the U{sup V} ion in complex fluorides of the type M{sub 3}UF{sub 8} (M = NH{sub 4}, Na, Rb, Cs) leads to an interpretation based on a trigonal deformation of the eight fluorine atom structure surrounding the uranium atom. By applying a Hamiltonian spin formalism and making a systematic use of group theory, it is possible to present the susceptibility calculations very concisely. Study of the resonance and of the relaxation of the fluorine atoms in powdered uranium VI complex fluorides suggests a structural model in the case of NaUF{sub 7}. It is shown that the shape of the magnetic resonance absorption lines is strongly affected by the presence of large anisotropic chemical shifts. In the model proposed here, six fluorine atoms are linked to the uranium, atom by strongly covalent bonds in a deformed UF{sub 6} octahedral structure; the seventh fluorine atom remains ionic. The occurrence of a rotational movement of the octahedron is confirmed by a study of the longitudinal relaxation of the fluorine atoms, the activation energy being 0.46 eV. (author) [French] L'etude de la susceptibilite magnetique de complexes fluores d'uranium V et la resonance magnetique des fluors dans des complexes fluores d'uranium VI permettent de proposer un modele structural pour ces composes, ou la diffraction des rayons X, en l'absence de monocristaux convenables, est incapable de preciser la position des atomes de

  11. A coupled mass transfer and surface complexation model for uranium (VI) removal from wastewaters

    International Nuclear Information System (INIS)

    Lenhart, J.; Figueroa, L.A.; Honeyman, B.D.

    1994-01-01

    A remediation technique has been developed for removing uranium (VI) from complex contaminated groundwater using flake chitin as a biosorbent in batch and continuous flow configurations. With this system, U(VI) removal efficiency can be predicted using a model that integrates surface complexation models, mass transport limitations and sorption kinetics. This integration allows the reactor model to predict removal efficiencies for complex groundwaters with variable U(VI) concentrations and other constituents. The system has been validated using laboratory-derived kinetic data in batch and CSTR systems to verify the model predictions of U(VI) uptake from simulated contaminated groundwater

  12. Uranium mineralization in the ring complex of Taperuaba, CE, Brazil

    International Nuclear Information System (INIS)

    Haddad, R.C.

    1981-01-01

    The study of the uraniferous deposit in the Northeast has been increased in last year, because of the discovery of many anomalies containing phosphate uraniferous mineralization. The anomalies in vila de Taperuaba at Ceara were examined. The petrografic, structural and geochemical study of the Taperuaba Ring complex, is made, in an attempt to estabilish the ore genesis and its probable controls. (L.H.L.L.) [pt

  13. Characterization of the sorption of uranium(VI) on different complexing resins

    International Nuclear Information System (INIS)

    Pesavento, Maria; Biesuz, Raffaela; Alberti, Giancarla; Sturini, Michela

    2003-01-01

    The sorption of uranium(VI) on two cationic resins containing different complexing groups, the iminodiacetic resin Chelex 100 and the weak carboxylic resin Amberlite CG-50, was investigated. The Gibbs-Donnan model was used to describe and to predict the sorption through the determination of the intrinsic complexation constants. These quantities, even though non-thermodynamic, characterize the sorption as being independent of experimental conditions. The sorption mechanism of the metal on the complexing resins was also studied by adding a competitive soluble ligand that shifts the sorption curves to higher pH values. The ligand competes with the resin for the complexation with the metal ion. Uranium is also strongly sorbed on Chelex 100 at very acid pH, through formation of two complexes in the resin phase: ML with logβ 110i =-1.16, in more acidic solution, and ML 2 with log β 120i =-5.72. Only the presence of the competitive ligand in solution makes the determination of the second complex possible. Also on Amberlite CG-50 the sorption is strong and involves the formation of the complex ML 2 , in more acidic solution, with log β 120i =-3.16. In the presence of the ligand EDTA, the complex ML 2 (OH) 2 was characterized with log β 12-2i =-5.15. In all the experiments the hydrolysis reaction in the aqueous phase was quantitatively considered. (orig.)

  14. The uranium potential of the Bushveld Complex, South Africa

    International Nuclear Information System (INIS)

    Simpson, P.R.

    1986-04-01

    This paper presents a summary on much of the existing geochemical data on the siliceous components of the Bushveld Complex (i.e., the felsites, granophyres and granites) with a view to establishing the U potential of the district. Although very few U analyses are actually available, sophisticated normalised data plots are utilized to estimate the probable U contents of the rock types. The members of the siliceous suite exhibit a gradual chemical evolution through time and illustrates that the most evolved members of the suite probably contained the highest primary U contents. It is emphasized that most known Bushveld Sn and F occurrences, with which U is likely to be associated, and most of the recognized radiometric anomalies in the complex, are concentrated along major lineaments. In this respect the Murchison and Franspoort directions are considered to be particularly important. In conclusion the argument follows that the potential for undiscovered hydrothermal U ores in the Bushveld Complex is high, and that five factors will probably control the location of such deposits. These factors include: 1. Sn, F and LIL-enriched source granite; 2. High post-emplacement heat production to promote the development of post-emplacement mineralizing systems; 3. A tectonically unstable source region with major fracture zones; 4. Suitable trap environments in the granites and their country rocks; 5. A source of fluids from aquifers in the granite aureole

  15. Alecto - results obtained with homogeneous critical experiments on plutonium 239, uranium 235 and uranium 233; Alecto - resultats des experiences critiques homogenes realisees sur le plutonium 239, l'uranium 235 et l'uranium 233

    Energy Technology Data Exchange (ETDEWEB)

    Bruna, J G; Brunet, J P; Caizegues, R; Clouet d' Orval, Ch; Kremser, J; Tellier, H; Verriere, Ph [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1965-07-01

    In this report are given the results of the homogeneous critical experiments ALECTO, made on plutonium 239, uranium 235 and uranium 233. After a brief description of the equipment, the critical masses for cylinders of diameters varying from 25 to 42 cm, are given and compared with other values (foreign results, criticality guide). With respect to the specific conditions of neutron reflection in the ALECTO experiments the minimal values of critical masses are: Pu239 M{sub c} = 910 {+-} 10 g, U235 M{sub c} = 1180 {+-} 12 g and U233 M{sub c} = 960 {+-} 10 g. Experiments relating to cross sections and constants to be used on these materials are presented. Lastly, kinetic experiments allow to compare pulsed neutron methods to fluctuation methods. [French] On presente dans ce rapport les resultats des experiences critiques homogenes ALECTO, effectuees sur le plutonium 239, l'uranium 235 et l'uranium 233. Apres avoir rappele la description des installations, on donne les masses critiques pour des cylindres de diametres variant entre 25 et 42 cm, qui sont comparees avec d'autres chiffres (resultats etrangers, guide de criticite). Dans les gammes des diametres etudies pour des cuves a fond plat reflechies lateralement, la valeur minimale des masses critiques est la suivante: Pu239 M{sub c} = 910 {+-} 10 g, U235 M{sub c} = 1180 {+-} 12 g et U233 M{sub c} 960 {+-} 10 g. Des experiences portant sur les sections efficaces et les constantes a utiliser sur ces milieux sont ensuite presentees. Enfin des experiences de cinetique permettent une comparaison entre la methode des neutrons pulses et la methode des fluctuations. (auteur)

  16. Extraction of uranium (VI) sulphate complexes by Adogen amines

    Energy Technology Data Exchange (ETDEWEB)

    Elyamani, I S; Abd Elmessieh, E N [Nuclear chemistry department, hot laboratories center, atomic energy authority, Cairo, (Egypt)

    1995-10-01

    The distribution of U(VI) between aqueous H{sub 2} So{sub 4} solutions and organic phases of adogen-368 has been described. The dependence of extraction on acidity, diluent type, metal and extractant concentrations was investigated. The possible extraction mechanism is discussed in the light of results obtained. The separation of U(VI) from rare earths is suggested. 5 figs., 1 tab.

  17. Uranium

    International Nuclear Information System (INIS)

    Battey, G.C.; McKay, A.D.

    1988-01-01

    Production for 1986 was 4899 t U 3 O 8 (4154 t U), 30% greater than in 1985, mainly because of a 39% increase in production at Ranger. Exports for 1986 were 4166 t U 3 O 8 at an average f.o.b. unit value of $40.57/lb U 3 O 8 . Private exploration expenditure for uranium in Australia during the 1985-86 fiscal year was $50.2 million. Plans were announced to increase the nominal capacity of the processing plant at Ranger from 3000 t/year U 3 O 8 to 4500 t and later to 6000 t/year. Construction and initial mine development at Olympic Dam began in March. Production is planned for mid 1988 at an annual rate of 2000 t U 3 O 8 , 30 000 t Cu, and 90 000 oz (2800 kg) Au. The first long-term sales agreement was concluded in September 1986. At the Manyingee deposit, testing of the alkaline solution mining method was completed, and the treatment plant was dismantled. Spot market prices (in US$/lb U 3 O 8 ) quoted by Nuexco were generally stable. From January-October the exchange value fluctuated from US$17.00-US$17.25; for November and December it was US$16.75. Australia's Reasonably Assured Resources of uranium recoverable at less than US$80/kg U at December 1986 were estimated as 462 000 t U, 3000 t U less than in 1985. This represents 30% of the total low-cost RAR in the WOCA (World Outside the Centrally Planned Economy Areas) countries. Australia also has 257 000 t U in the low-cost Estimated Additional Resources Category I, 29% of the WOCA countries' total resources in this category

  18. Effects of solution pH and complexing reagents on uranium and thorium desorption under saturated equilibrium conditions

    International Nuclear Information System (INIS)

    Wang, Yug-Yea; Yu, C.

    1992-01-01

    Three contaminated bulk surface soils were used for investigating the effect of solution pH and complexing reagents on uranium and thorium desorption. At a low solution pH, the major chemical species of uranium and thorium, uranyl UO 2 +2 , thorium dihydroxide Th(OH) 2 +2 , and thorium hydroxide Th(OH) +3 , tend to form complexes with acetates in the solution phase, which increases the fractions of uranium and thorium desorbed into this phase. At a high solution pH, important uranium and thorium species such as uranyl tricarbonate complex UO 2 (CO) 33 -4 and thorium tetrahydroxide complex Th(OH) 4 tend to resist complexation with acetates. The presence of complexing reagents in solution can release radionuclides such as uranium and/or thorium from the soil to the solution by forming soluble complexes. Sodium bicarbonate (NaHCO 3 ) and diethylenetriaminepentaacetic acid (DTPA) are strong complex formers that released 38% to 62% of total uranium activity and 78% to 86% of total thorium activity, respectively, from the soil samples investigated. Solutions of 0.1 molar sodium nitrate (NaNO 3 ) and 0.1 molar sodium sulfate (Na 2 SO 4 ) were not effective complex formers with uranium and thorium under the experimental conditions. Fractions of uranium and thorium desorbed by 0.15g/200ml humic acid ranged from 4.62% to 6.17% and 1.59% to 7.09%, respectively. This work demonstrates the importance of a knowledge of solution chemistry in investigating the desorption of radionuclides

  19. Development of complex electrokinetic decontamination method for soil contaminated with uranium

    International Nuclear Information System (INIS)

    Kim, Gye-Nam; Kim, Seung-Soo; Park, Hye-Min; Kim, Wan-Suk; Moon, Jei-Kwon; Hyeon, Jay-Hyeok

    2012-01-01

    520L complex electrokinetic soil decontamination equipment was manufactured to clean up uranium contaminated soils from Korean nuclear facilities. To remove uranium at more than 95% from the radioactive soil through soil washing and electrokinetic technology, decontamination experiments were carried out. To reduce the generation of large quantities of metal oxides in cathode, a pH controller is used to control the pH of the electrolyte waste solution between 0.5 and 1 for the formation of UO 2+ . More than 80% metal oxides were removed through pre-washing, an electrolyte waste solution was circulated by a pump, and a metal oxide separator filtered the metal oxide particles. 80–85% of the uranium was removed from the soil by soil washing as part of the pre-treatment. When the initial uranium concentration of the soil was 21.7 Bq/g, the required electrokinetic decontamination time was 25 days. When the initial concentration of 238 U in the soil was higher, a longer decontamination time was needed, but the removal rate of 238 U from the soil was higher.

  20. Radiological and environmental safety aspects of uranium fuel fabrication plants at Nuclear Fuel Complex, Hyderabad

    International Nuclear Information System (INIS)

    Viswanathan, S.; Surya Rao, B.; Lakshmanan, A.R.; Krishna Rao, T.

    1991-01-01

    Nuclear Fuel Complex, Hyderabad manufactures uranium dioxide fuel assemblies for PHWRs and BWRs operating in India. Starting materials are magnesium diuranate received from UCIL, Jaduguda and imported UF. Both of these are converted to UO 2 pellets by identical chemical processes and mechanical compacting. Since the uranium handled here is free of daughter product activities, external radiation is not a problem. Inhalation of airborne U compounds is one of the main source of exposure. Engineered protective measures like enclosures around U bearing powder handling equipment and local exhausts reduce worker's exposure. Installation of pre-filters, wet rotoclones and electrostatic precipitators in the ventillation system reduces the release of U into the environment. The criticality hazard in handling slightly enriched uranium is very low due to the built-in control based on geometry and inventory. Where airborne uranium is significant, workers are provided with protective respirators. The workers are regularly monitored for external exposure and also for internal exposure. The environmental releases from the NFC facility is well controlled. Soil, water and air from the NFC environment are routinely collected and analysed for all the possible pollutants. The paper describes the Health Physics experience during the last five years on occupational exposures and on environmental surveillance which reveals the high quality of safety observed in our nuclear fuel fabricating installations. (author). 4 refs., 6 tabs

  1. Reactions of uranium (III) and (IV) compounds with ketones, nitriles and acid chlorides. Towards a use of uranium complexes in organic synthesis

    International Nuclear Information System (INIS)

    Adam, Raymond

    1993-01-01

    In this research thesis, the author shows that various organic molecules can be interestingly transformed into uranium complexes with degrees of oxidation of +3 or +4. In a first part, the author describes reactions of carbonyl compounds with the UCl 4 -Na(Hg) reducing system. Then, he addresses reductions of ketones, nitriles and acid chlorides by a uranium (III) complex: Cp 3 U(THF). The third part reports a detailed study of the reduction of ketones by U(BH 4 ) 4 [fr

  2. Agpaitic nepheline syenites from the Ilimaussaq Complex, south Greenland; an important new uranium ore type (v.2)

    International Nuclear Information System (INIS)

    Mair, J.L.; Bunn, S.

    2010-01-01

    The Ilimaussaq Intrusive Complex in south Greenland is a layered alkaline igneous body that is predominantly comprised of agpaitic nepheline syenites. The Complex is now recognized as containing vast resources of uranium in polymetallic ores that are also strongly enriched in rare earth elements (REEs) and zinc. Uranium and REEs are dominantly hosted in phosphate minerals with a minor proportion hosted in zirconium silicate minerals. Equivalent ores are yet to be mined for uranium anywhere in the world; however, studies are well advanced in confirming a process route to economically extract uranium. The Ilimaussaq Complex is considered the world's type-locality for agpaitic rocks. Formation of the complex is attributed to four successive pulses of magma. The first produced an augite syenite, which now forms a marginal shell. This was followed by intrusion of a sheet of peralkaline granite. The third and fourth stages make up the bulk of the intrusion and are peralkaline to hyper-agpaitic in composition. The third batch of magma differentiated to produce pulaskite, foyaite and naujaite. Stage four produced the kakortokites and lujavrites, which are the units of particular economic significance. Kakortokites are strongly enriched in zirconium, niobium and tantalum, whereas the lujavrites are strongly enriched in uranium, rare earth elements, fluorine and zinc. Lujavrites are vertically zoned with arfvedonsite (black) lujavrites grading downward into aegerine (green) lujavrites. The upper most portions of the black lujavrites contain uranium concentrations of greater than 450 ppm, which decreases downward over 200 - 300m toward green lujavrites where uranium concentrations rarely exceeds 200 ppm. Resources defined to date in accordance with the Australian JORC code include 192 million lb. of U_3O_8 at 350 ppm within an overall resource of 282 million lb. of uranium oxide at a grade of 280 ppm. With scope for several other similar sized resources within complex, the

  3. 'Pincer' dicarbene complexes of some early transition metals and uranium.

    Science.gov (United States)

    Pugh, David; Wright, Joseph A; Freeman, Sandra; Danopoulos, Andreas A

    2006-02-14

    The complexes [(C-N-C)MX(n)(thf)(m)] with the 'pincer' 2,6-bis(imidazolylidene)pyridine, (C-N-C) = 2,6-bis(arylimidazol-2-ylidene)pyridine, aryl = 2,6-Pr(i)2C6H3, M = V, X = Cl, n = 2, m = 1 1a; M = Cr, X = Cl, n = 2, m = 0, 2a, X = Br, 2b; M = Mn, X = Br, n = 2, m = 0, 3; M = Nb, X = Cl, n = 3, m = 0, 4; and M = U, X = Cl, n = 4, m = 0, 5, were synthesised by (a) substitution of labile tmed (1a), thf (2a, 3, 5) or dme (4) by free (C-N-C) or by (b) reaction of the bisimidazolium salt (CH-N-CH)Br2 with {Cr[N(SiMe3)2]2(thf)2} followed by amine elimination (2b). Attempted alkylation of 1a, 2, 3a and 4 with Grignard or alkyl lithiums gave intractable mixtures, and in one case [reaction of 1a with (mesityl)MgBr] resulted in exchange of Cl by Br (1b). Oxidation of 1a or [(C-N-C)VCl3] with 4-methylmorpholine N-oxide afforded the trans-V(C-N-C)(=O)Cl2, 6, which by reaction with AgBF4 in MeCN gave trans-[V(C-N-C)(=O)(MeCN)2][BF4]2, 7. Reaction of 1a with p-tolyl azide gave trans-V(C-N-C)(=N-p-tolyl)Cl2 8. The complex trans-Ti(C-N-C)(=NBu(t))Cl2, 9, was prepared by substitution of the pyridine ligands in Ti(NBu(t))Cl2(py)3 by C-N-C.

  4. Procedure for recovery from an uranium containing concentrate and phosphoric acid, as well as an uranium containing concentrate and phosphoric acid obtained by this procedure

    International Nuclear Information System (INIS)

    1980-01-01

    The phosphate ore is dissolved in sulphuric acid and the formed calcium sulphate is separated from the solution. The uranium is then precipitated by adding ammonium fluoride solution to the remaining phosphoric acid solution. When the phosphate ore is dissolved in sulphuric acid, fluorine gas is liberated and this is then used to produce the ammonium fluoride solution. (Th.P.)

  5. A direct algebraic method applied to obtain complex solutions of some nonlinear partial differential equations

    International Nuclear Information System (INIS)

    Zhang Huiqun

    2009-01-01

    By using some exact solutions of an auxiliary ordinary differential equation, a direct algebraic method is described to construct the exact complex solutions for nonlinear partial differential equations. The method is implemented for the NLS equation, a new Hamiltonian amplitude equation, the coupled Schrodinger-KdV equations and the Hirota-Maccari equations. New exact complex solutions are obtained.

  6. New South African complex leaches gold, uranium, and sulphur from slimes

    Energy Technology Data Exchange (ETDEWEB)

    Payne, A.

    1978-01-01

    Slimes dams at various mines in the Orange Free State and the Transvaal are being re-treated to recover U, Au, and H/sub 2/SO/sub 4/. Components of the Free State Metallurgical Complex include flotation plants, a uranium plant, the President Brand plant for H/sub 2/SO/sub 4/ production from the pyrite concentrates, and a calcine leaching plant for producing gold from the calcines of the acid plant. Reasons for the complex and its operation are discussed. (DLC)

  7. Complex formation between uranium(VI) and α-D-glucose 1-phosphate

    International Nuclear Information System (INIS)

    Koban, A.; Geipel, G.; Bernhard, G.

    2003-01-01

    The complex formation of uranium(VI) with α-D-glucose 1-phosphate (C 6 H 11 O 6 PO 3 2- , G1P) was determined by time-resolved laser-induced fluorescence spectroscopy (TRLFS) at pH 4 and potentiometric titration in the pH range from 3 to 10. Both measurements show the formation of a 1 : 1 complex at lower pH values. The formation constant of UO 2 (C 6 H 11 O 6 PO 3 ) was calculated from TRLFS measurements to be log β 11 = 5.72±0.12, and from potentiometric titration log β 11 = 5.40±0.25, respectively. It was found by potentiometric titration that at higher pH values the complexation changes to a 1 : 2 complex. The stability constant for this complex was calculated to be log β 12 = 8.96±0.18. (orig.)

  8. Single-molecule magnetism in a single-ion triamidoamine uranium(V) terminal mono-oxo complex

    Energy Technology Data Exchange (ETDEWEB)

    King, David M.; McMaster, Jonathan; Lewis, William; Blake, Alexander J.; Liddle, Stephen T. [Nottingham Univ. (United Kingdom). School of Chemistry; Tuna, Floriana; McInnes, Eric J.L. [Manchester Univ. (United Kingdom). School of Chemistry

    2013-04-26

    Straightforward oxidation of a triamidoamine uranium(III) complex with trimethyl-N-oxide affords a uranium(V) terminal mono-oxo complex which is the first clear-cut example of a uranium(V) single-molecule magnet (SMM). This monometallic complex unambiguously shows that a strongly axially ligated and thus anisotropic ligand field can be used to overcome the limited magnetic anisotropy of uranium(V). [German] Die direkte Oxidation eines Triamidoamin-Uran(III)-Komplexes mit Trimethyl-N-oxid liefert einen terminalen Uran(V)-Mono(oxo)komplex, der das erste gesicherte Beispiel eines Uran(V)-Einzelmolekuelmagnets ist. Dieser monometallische Komplex zeigt eindeutig, dass ein starkes axiales und somit anisotropes Ligandenfeld die begrenzte magnetische Anisotropie von Uran(V) beseitigen kann.

  9. Investigation and analytical application of thorium and uranium complexes with amino acids

    International Nuclear Information System (INIS)

    Korenman, I.M.; Sergeev, G.M.

    1979-01-01

    The coordination is investigated of thorium (4) and uranium (6) with aminoacids, particularly, with aspartic acid. With the latter the metals form chelates, which have a particular structure and a stationary inner sphere. A description is made of the composition, conditions of formation (gr H), and a stability of some asparaginate complexes of actinoids, the coordination methods of aspartic acid. An asparaginatometric method is proposed for a direct complexometric titration of microgram amounts of thorium in the presence of uranium, zirconium and rare earth elements with photometric indication. As metal-chromic indicators the sulfophthaleins are applied. The given procedure allows measurement of impurities of accompanying elements, viz., beryllium (up to 1%) in thorium preparations. Application of aspartic acid and arsenazo 1 indicator permits us to define Be(2) with a relative error not higher than 5% in thorium compounds, which exclude the analysis by other methods

  10. Extraction of uranium from simulated ore by the supercritical carbon dioxide fluid extraction method with nitric acid-TBP complex

    International Nuclear Information System (INIS)

    Dung, Le Thi Kim; Imai, Tomoki; Tomioka, Osamu; Nakashima, Mikio; Takahashi, Kuniaki; Meguro, Yoshihiro

    2006-01-01

    The supercritical fluid extraction (SFE) method using CO 2 as a medium with an extractant of HNO 3 -tri-n-butyl phosphate (TBP) complex was applied to extract uranium from several uranyl phosphate compounds and simulated uranium ores. An extraction method consisting of a static extraction process and a dynamic one was established, and the effects of the experimental conditions, such as pressure, temperature, and extraction time, on the extraction of uranium were ascertained. It was found that uranium could be efficiently extracted from both the uranyl phosphates and simulated ores by the SFE method using CO 2 . It was thus demonstrated that the SFE method using CO 2 is useful as a pretreatment method for the analysis of uranium in ores. (author)

  11. Recycled Uranium Mass Balance Project Y-12 National Security Complex Site Report

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2000-12-01

    This report has been prepared to summarize the findings of the Y-12 National Security Complex (Y-12 Complex) Mass Balance Project and to support preparation of associated U. S. Department of Energy (DOE) site reports. The project was conducted in support of DOE efforts to assess the potential for health and environmental issues resulting from the presence of transuranic (TRU) elements and fission products in recycled uranium (RU) processed by DOE and its predecessor agencies. The United States government used uranium in fission reactors to produce plutonium and tritium for nuclear weapons production. Because uranium was considered scarce relative to demand when these operations began almost 50 years ago, the spent fuel from U.S. fission reactors was processed to recover uranium for recycling. The estimated mass balance for highly enriched RU, which is of most concern for worker exposure and is the primary focus of this project, is summarized in a table. A discrepancy in the mass balance between receipts and shipments (plus inventory and waste) reflects an inability to precisely distinguish between RU and non-RU shipments and receipts involving the Y-12 Complex and Savannah River. Shipments of fresh fuel (non-RU) and sweetener (also non-RU) were made from the Y-12 Complex to Savannah River along with RU shipments. The only way to distinguish between these RU and non-RU streams using available records is by enrichment level. Shipments of {le}90% enrichment were assumed to be RU. Shipments of >90% enrichment were assumed to be non-RU fresh fuel or sweetener. This methodology using enrichment level to distinguish between RU and non-RU results in good estimates of RU flows that are reasonably consistent with Savannah River estimates. Although this is the best available means of distinguishing RU streams, this method does leave a difference of approximately 17.3 MTU between receipts and shipments. Slightly depleted RU streams received by the Y-12 Complex from ORGDP and

  12. Uranium (VI) complexing by macrocyclic or chelating ligands in aqueous solutions stability, formation kinetics, polarographic properties

    International Nuclear Information System (INIS)

    Brighli, M.

    1984-07-01

    Stability of chelates (with EDTA,N,N ethylenediamine diacetic acid EDDA nitrilotriacetic acid NTA and iminodiacetic acid) of UO 2 2+ and UO 4 species of uranium VI is studied in aqueous solution (NaClO 4 3M at 25 deg celcius). Structure in solution are proposed and discussed for mononuclear species. Only complexing kinetics (formation and acid hydrolysis) of UO 4 with EDDA and NTA are studied by spectrophotometry (other reactions are too fast). Besides UO 2 2+ complexes are formed with crown ethers I5C5 and I8C6 in aqueous solution (TEA ClO 4 M/10 at 25 deg celcius. Complexes are probably stabilized by solvation. Results are confirmed by voltametry and reduction mechanisms of UO 2 2+ and its complexes on mercury drop are proposed. 143 refs [fr

  13. Synthesis and characterization of thorium(IV) and uranium(IV) complexes with Schiff bases

    Energy Technology Data Exchange (ETDEWEB)

    Radoske, Thomas; Maerz, Juliane; Kaden, Peter; Patzschke, Michael; Ikeda-Ohno, Atsushi [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Chemistry of the F-Elements

    2017-06-01

    We report herein the synthesis and characterization of several imine complexes of tetravalent thorium (Th(IV)) and uranium (U(IV)). The ligands investigated in this study are a Schiff base type, including the well-known salen ligand (H{sub 2}Le, Fig. 1). The complexation in solution was investigated by NMR measurements indicating paramagnetic effects of unpaired f-electrons of U(IV) on the ligand molecule. We also determined the solid-state molecular structures of the synthesized complexes by single crystal X-ray diffraction. The synthesized complexes show an eight-fold coordination geometry around the actinide center surrounded by two tetradentate ligands with 2N- and 2O-donor atoms.

  14. Tetra- and hexavalent uranium forms bidentate-mononuclear complexes with particulate organic matter in a naturally uranium-enriched peatland

    International Nuclear Information System (INIS)

    Mikutta, Christian; Langner, Peggy; Bargar, John R.; Kretzschmar, Ruben

    2016-01-01

    Peatlands frequently serve as efficient biogeochemical traps for U. Mechanisms of U immobilization in these organic matter-dominated environments may encompass the precipitation of U-bearing mineral(oid)s and the complexation of U by a vast range of (in)organic surfaces. The objective of this work was to investigate the spatial distribution and molecular binding mechanisms of U in soils of an alpine minerotrophic peatland (pH 4.7–6.6, E_h = –127 to 463 mV) using microfocused X-ray fluorescence spectrometry and bulk and microfocused U L_3-edge X-ray absorption spectroscopy. The soils contained 2.3–47.4 wt % organic C, 4.1–58.6 g/kg Fe, and up to 335 mg/kg geogenic U. Uranium was found to be heterogeneously distributed at the micrometer scale and enriched as both U(IV) and U(VI) on fibrous and woody plant debris (48 ± 10% U(IV), x̄ ± σ, n = 22). Bulk U X-ray absorption near edge structure (XANES) spectroscopy revealed that in all samples U(IV) comprised 35–68% of total U (x̄ = 50%, n = 15). Shell-fit analyses of bulk U L_3-edge extended X-ray absorption fine structure (EXAFS) spectra showed that U was coordinated to 1.3 ± 0.2 C atoms at a distance of 2.91 ± 0.01 Å (x̄ ± σ), which implies the formation of bidentate-mononuclear U(IV/VI) complexes with carboxyl groups. We neither found evidence for U shells at ~3.9 Å, indicative of mineral-associated U or multinuclear U(IV) species, nor for a substantial P/Fe coordination of U. As a result, our data indicates that U(IV/VI) complexation by natural organic matter prevents the precipitation of U minerals as well as U complexation by Fe/Mn phases at our field site, and suggests that organically complexed U(IV) is formed via reduction of organic matter-bound U(VI).

  15. Tetra- and Hexavalent Uranium Forms Bidentate-Mononuclear Complexes with Particulate Organic Matter in a Naturally Uranium-Enriched Peatland.

    Science.gov (United States)

    Mikutta, Christian; Langner, Peggy; Bargar, John R; Kretzschmar, Ruben

    2016-10-04

    Peatlands frequently serve as efficient biogeochemical traps for U. Mechanisms of U immobilization in these organic matter-dominated environments may encompass the precipitation of U-bearing mineral(oid)s and the complexation of U by a vast range of (in)organic surfaces. The objective of this work was to investigate the spatial distribution and molecular binding mechanisms of U in soils of an alpine minerotrophic peatland (pH 4.7-6.6, E h = -127 to 463 mV) using microfocused X-ray fluorescence spectrometry and bulk and microfocused U L 3 -edge X-ray absorption spectroscopy. The soils contained 2.3-47.4 wt % organic C, 4.1-58.6 g/kg Fe, and up to 335 mg/kg geogenic U. Uranium was found to be heterogeneously distributed at the micrometer scale and enriched as both U(IV) and U(VI) on fibrous and woody plant debris (48 ± 10% U(IV), x̅ ± σ, n = 22). Bulk U X-ray absorption near edge structure (XANES) spectroscopy revealed that in all samples U(IV) comprised 35-68% of total U (x̅ = 50%, n = 15). Shell-fit analyses of bulk U L 3 -edge extended X-ray absorption fine structure (EXAFS) spectra showed that U was coordinated to 1.3 ± 0.2 C atoms at a distance of 2.91 ± 0.01 Å (x̅ ± σ), which implies the formation of bidentate-mononuclear U(IV/VI) complexes with carboxyl groups. We neither found evidence for U shells at ∼3.9 Å, indicative of mineral-associated U or multinuclear U(IV) species, nor for a substantial P/Fe coordination of U. Our data indicates that U(IV/VI) complexation by natural organic matter prevents the precipitation of U minerals as well as U complexation by Fe/Mn phases at our field site, and suggests that organically complexed U(IV) is formed via reduction of organic matter-bound U(VI).

  16. Synthesis, characterization, and reactivity of a uranium(VI) carbene imido oxo complex

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Erli; Cooper, Oliver J.; McMaster, Jonathan; Lewis, William; Blake, Alexander J.; Liddle, Stephen T. [Nottingham Univ. (United Kingdom). School of Chemistry; Tuna, Floriana; McInnes, Eric J.L. [Manchester Univ. (United Kingdom). School of Chemistry and Photon Science Inst.

    2014-06-23

    We report the uranium(VI) carbene imido oxo complex [U(BIPM{sup TMS})(NMes)(O)(DMAP){sub 2}] (5, BIPM{sup TMS}=C(PPh{sub 2}NSiMe{sub 3}){sub 2}; Mes=2,4,6-Me{sub 3}C{sub 6}H{sub 2}; DMAP=4-(dimethylamino)pyridine) which exhibits the unprecedented arrangement of three formal multiply bonded ligands to one metal center where the coordinated heteroatoms derive from different element groups. This complex was prepared by incorporation of carbene, imido, and then oxo groups at the uranium center by salt elimination, protonolysis, and two-electron oxidation, respectively. The oxo and imido groups adopt axial positions in a T-shaped motif with respect to the carbene, which is consistent with an inverse trans-influence. Complex 5 reacts with tert-butylisocyanate at the imido rather than carbene group to afford the uranyl(VI) carbene complex [U(BIPM{sup TMS})(O){sub 2}(DMAP){sub 2}] (6).

  17. Synthesis, characterization, and reactivity of a uranium(VI) carbene imido oxo complex

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Erli; Cooper, Oliver J.; McMaster, Jonathan; Lewis, William; Blake, Alexander J.; Liddle, Stephen T. [School of Chemistry, University of Nottingham (United Kingdom); Tuna, Floriana; McInnes, Eric J.L. [School of Chemistry and Photon Science Institute, University of Manchester (United Kingdom)

    2014-06-23

    We report the uranium(VI) carbene imido oxo complex [U(BIPM{sup TMS})(NMes)(O)(DMAP){sub 2}] (5, BIPM{sup TMS}=C(PPh{sub 2}NSiMe{sub 3}){sub 2}; Mes=2,4,6-Me{sub 3}C{sub 6}H{sub 2}; DMAP=4-(dimethylamino)pyridine) which exhibits the unprecedented arrangement of three formal multiply bonded ligands to one metal center where the coordinated heteroatoms derive from different element groups. This complex was prepared by incorporation of carbene, imido, and then oxo groups at the uranium center by salt elimination, protonolysis, and two-electron oxidation, respectively. The oxo and imido groups adopt axial positions in a T-shaped motif with respect to the carbene, which is consistent with an inverse trans-influence. Complex 5 reacts with tert-butylisocyanate at the imido rather than carbene group to afford the uranyl(VI) carbene complex [U(BIPM{sup TMS})(O){sub 2}(DMAP){sub 2}] (6). (copyright 2014 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  18. Cation-mediated conversion of the state of charge in uranium arene inverted-sandwich complexes

    Energy Technology Data Exchange (ETDEWEB)

    Camp, Clement; Mougel, Victor; Pecaut, Jacques; Mazzanti, Marinella [Laboratoire de Reconnaissance Ionique et Chimie de Coordination, SCIB, UMR-E3 CEA-UJF, INAC, CEA-Grenoble (France); Maron, Laurent [LCPNO, CNRS and INSA, UPS, Universite de Toulouse (France)

    2013-12-16

    Two new arene inverted-sandwich complexes of uranium supported by siloxide ancillary ligands [K{U(OSi(OtBu)_3)_3}{sub 2}(μ-η{sup 6}:η{sup 6}-C{sub 7}H{sub 8})] (3) and [K{sub 2}{U(OSi(OtBu)_3)_3}{sub 2}(μ-η{sup 6}:η{sup 6}-C{sub 7}H{sub 8})] (4) were synthesized by the reduction of the parent arene-bridged complex [{U(OSi(OtBu)_3)_3}{sub 2}(μ-η{sup 6}:η{sup 6}-C{sub 7}H{sub 8})] (2) with stoichiometric amounts of KC{sub 8} yielding a rare family of inverted-sandwich complexes in three states of charge. The structural data and computational studies of the electronic structure are in agreement with the presence of high-valent uranium centers bridged by a reduced tetra-anionic toluene with the best formulation being U{sup V}-(arene{sup 4-})-U{sup V}, KU{sup IV}-(arene{sup 4-})-U{sup V}, and K{sub 2}U{sup IV}-(arene{sup 4-})-U{sup IV} for complexes 2, 3, and 4 respectively. The potassium cations in complexes 3 and 4 are coordinated to the siloxide ligands both in the solid state and in solution. The addition of KOTf (OTf=triflate) to the neutral compound 2 promotes its disproportionation to yield complexes 3 and 4 (depending on the stoichiometry) and the U{sup IV} mononuclear complex [U(OSi(OtBu){sub 3}){sub 3}(OTf)(thf){sub 2}] (5). This unprecedented reactivity demonstrates the key role of potassium for the stability of these complexes. (Copyright copyright 2013 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  19. Characterization of the sorption of uranium(VI) on different complexing resins

    Energy Technology Data Exchange (ETDEWEB)

    Pesavento, Maria; Biesuz, Raffaela; Alberti, Giancarla; Sturini, Michela [Dipartimento di Chimica Generale dell' Universita degli Studi di Pavia, Via Taramelli 12, 27100, Pavia (Italy)

    2003-08-01

    The sorption of uranium(VI) on two cationic resins containing different complexing groups, the iminodiacetic resin Chelex 100 and the weak carboxylic resin Amberlite CG-50, was investigated. The Gibbs-Donnan model was used to describe and to predict the sorption through the determination of the intrinsic complexation constants. These quantities, even though non-thermodynamic, characterize the sorption as being independent of experimental conditions. The sorption mechanism of the metal on the complexing resins was also studied by adding a competitive soluble ligand that shifts the sorption curves to higher pH values. The ligand competes with the resin for the complexation with the metal ion. Uranium is also strongly sorbed on Chelex 100 at very acid pH, through formation of two complexes in the resin phase: ML with log{beta}{sub 110i}=-1.16, in more acidic solution, and ML{sub 2}with log {beta}{sub 120i}=-5.72. Only the presence of the competitive ligand in solution makes the determination of the second complex possible. Also on Amberlite CG-50 the sorption is strong and involves the formation of the complex ML {sub 2}, in more acidic solution, with log {beta}{sub 120i}=-3.16. In the presence of the ligand EDTA, the complex ML {sub 2}(OH) {sub 2}was characterized with log {beta}{sub 12-2i}=-5.15. In all the experiments the hydrolysis reaction in the aqueous phase was quantitatively considered. (orig.)

  20. Thorium and uranium separation from Rare Earth complex minerals in Turkey

    International Nuclear Information System (INIS)

    Uzmen, R.

    2014-01-01

    Conclusion: • Thorium and uranium separation from a REEs solution is possible in by using simple traditional methods. • Main advantage of this method is to separate with high recovery yield uraniumand almost completely thorium which is an undesirable element due to its radioactive property in the different REEs group or individual REE. • Separation of thorium before any other step of REE’s group or individual element separation is crucial. • By using this flowsheet it would be possible to obtain uranium and other valuable elements (Zr, Ti, etc.) as coproducts of REEs. • Another important point, during REEs production, it is avoided to accumalate U and Th contaminated process wastes. • Thus, in the contrary, radioactive elements are refined and contained for safe storage.

  1. The use of tetracycline as complexing agent for the separation of interfering elements during uranium activation analysis

    International Nuclear Information System (INIS)

    Petrauskas, R.

    1984-01-01

    A method was developed for uranium separation, when its determination could not be performed by non-destructive neutron activation analysis due to the presence of interfering elements. Th, Zn, Na, Ta, Fe, W, Mo, Ag and the lanthanides were considered interferents because some of these elements, via (n, γ) reactions, form the same radioisotopes produced in the fission of 235 U, or radioisotopes that emit gamma-rays with energies close to the ones emitted by 239 Np or by the fission products of 235 U. Besides they could form radioisotopes whose Compton continuum makes difficult the detection of the gamma-rays of 239 Np and the fission products of 235 U. The separation method is based on the extraction of uranium from the interfering elements using a solution of tetracycline in benzyl alcohol. Adequate conditions for the separation were studied and extraction curves of uranium and interferents were obtained separately and in the presence of a solution of uranium ore from the IAEA. Separation of uranium from Na, Ag and Zn was achieved with a single extraction operation and by controlling the pH of the aqueous phase. Diethylenetriaminepentaacetic acid was used as masking agent for uranium separation from Fe, Th and lanthanides. For other elements, the separation was partial, meaning that about 11% of W, 32% of Mo and 5% of Ta were extracted together with uranium after two extraction operations (extraction and washing). Chemical separation presented a recovery of 97% for uranium. After separation an aliquot of organic phase containing uranium was irradiated for uranium and isotopic ratio 235 U/ 238 U determinations. This method was applied in the analysis of the following ores: standard S-7 (pitchblende) provided by IAEA, monazite and an ore called 'goianita' from the state of Goias (GO, Brazil). The accuracy and precision of results were discussed, and the isotopic ratio results indicated that the ores analysed present an isotopic abundance of natural uranium. (Author

  2. Exploration of Bernabe Montano complex of uranium deposits, New Mexico, USA

    International Nuclear Information System (INIS)

    Porter, D.A.

    1981-01-01

    The Bernabe Montano discovery is a significant eastern extension of the Grants Mineral Belt, consisting of two nearly parallel mineralized trends with a combined strike length of about 14.5 km. One deposit with approximately 10 6 lb of uranium oxide has been blocked out and several km of mineralized trend require additional delineation drilling. The mineralization exhibits many similarities to Westwater Canyon Member ore deposits in other parts of the Grants Mineral Belt; one of the most significant is the continuation of the south-easterly trend that has persisted, with some breaks, for a length of over 175 km. As with other Grants Mineral Belt deposits, the mineralization is associated with multilevel humate masses that are roughly parallel to the bedding of the Westwater Canyon Member host sandstone beds. These humate masses and the associated uranium deposits show a marked preference for the margins of the thicker, more laterally continuous, channelways. The discovery of the Bernabe Montano complex of deposits is significant for several reasons. First, it opened up exploration in the distal fan facies where many geologists thought the uranium potential was relatively low. The discovery is potentially more significant in that it demonstrates the ability of detailed subsurface geologic mapping to suggest the location of high potential geologic trends in partially explored but favourable regions where the more traditional surface geologic and radiometric techniques are no longer effective in finding new deposits. (author)

  3. Indoor radon related to uranium in granitoids of the Central Bohemian plutonic complex

    International Nuclear Information System (INIS)

    Barnet, I.; Fojtikova, I.

    2004-01-01

    The study is based on the indoor radon data (one year measurements, Kodak LR 115 track etch detectors), vectorized geological maps 1:50000, vectorized coordinates of dwellings and uranium data for granitoid types of the Central Bohemian Plutonic Complex (CBPC). Using ArcGis 8.2 programme, the position of 16145 dwellings was linked to a geological database covering the CBPC (approx. 3200 km 2 ), and the type of underlying rock type was specified for each house. The resulting databases enabled us to calculate the mean EEC indoor Rn data for particular granitoid types and to study the relationship between the indoor Rn and the U concentrations. The petrogenetically variable CBPC was emplaced during Variscan orogenesis (330-350 Ma) and is among the most radioactive rock types within the Bohemian Massif. A long-term process of CBPC genesis resulted in more than 20 granitoid types, differing by their petrogenetic characteristics as well as mineralogical and chemical composition, including uranium concentration. The relation between the mean indoor radon values and uranium concentrations in particular rock types was examined. A positive regression between indoor Rn and uranium as the source of Rn soil gas clearly demonstrates how regional geology influences the indoor radon activity concentration in dwellings. The highest indoor Rn concentrations were observed in the Sedlcany granodiorite and Certovo bremeno syenite, where also the highest gamma dose rates (150-210 nGy.h -1 ) within all granitoid types in the Czech Republic were observed. The two rock types differ from other granitoids by a relatively high zircon concentration, which is the main source of U and subsequently of soil gas Rn being released from the bedrock. The lower indoor Rn values of Certovo bremeno syenite which do not correspond with the high U concentrations can be explained by a relatively low permeability of its clayey weathering crust. This feature was also observed for soil gas radon concentration

  4. Complexes carbéniques nucléophiles de l'uranium

    OpenAIRE

    Tourneux , Jean-Christophe

    2012-01-01

    The only stable f-metal carbene complexes (excluding NHC) metals f present R2C(2-) groups having one or two phosphorus atoms in the central carbon in alpha position. The objective of this work was to develop the chemistry of carbenes for uranium (metal 5f) with the dianion C{Ph2P(=S)}2(2-) (SCS(2-)) to extend the organometallic chemistry of this element in its various oxidation states (+3-6), and to reveal the influence of the 5f orbitals on the nature and reactivity of the double bond C=U.We...

  5. Southern complex: geology, geochemistry, mineralogy, and mineral chemistry of selected uranium- and thorium-rich granites

    International Nuclear Information System (INIS)

    Hoffman, M.A.

    1987-01-01

    Four major rock groups are defined in the Southern Complex: the Bell Creek Granite (BCG), the Clotted Granitoids (CGR), the Albite Granite (AGR), and the Migmatite Complex. Metatexites of the Migmatite Complex are the oldest rocks and include paleosome of a metasedimentary and metavolcanic protolith represented by Banded Iron Formation, Banded Amphibolite, and Banded Gneisses, and interlayered or crosscutting leucogranites. The CGR span the range from metatexite to diatexite and represent in-situ partial melting of metapelitic layers in the protolith during intrusion of the BCG. The BCG cuts the migmatites, is locally cut by the CGR, and was derived by partial melting of a dominantly metasedimentary protolith at some depth below the presently exposed migmatites during a regional tectonothermal event. The Albite Granite is a 2km diameter, muscovite-fluorite-columbite-bearing intrusive stock that cuts all other major units. The thorium history of the BCG is a function of the history of monazite. The thorium history of the CGR is also dominated by monazite but the thorium content of this unit cannot be entirely accounted for by original restite monazite. The uranium history of the BCG and CGR was dominated by magmatic differentiation and post magmatic, metamorphic and supergene redistributions and is largely independent of the thorium history. The thorium and uranium history of the AGR was dominated by magmatic/deuteric processes unlike the BCG and CGR

  6. A Highly Expressed High-Molecular-Weight S-Layer Complex of Pelosinus sp. Strain UFO1 Binds Uranium

    Energy Technology Data Exchange (ETDEWEB)

    Thorgersen, Michael P. [Univ. of Georgia, Athens, GA (United States). Dept. of Biochemistry and Molecular Biology; Lancaster, W. Andrew [Univ. of Georgia, Athens, GA (United States). Dept. of Biochemistry and Molecular Biology; Rajeev, Lara [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Biological Systems and Engineering Division; Ge, Xiaoxuan [Univ. of Georgia, Athens, GA (United States). Dept. of Biochemistry and Molecular Biology; Vaccaro, Brian J. [Univ. of Georgia, Athens, GA (United States). Dept. of Biochemistry and Molecular Biology; Poole, Farris L. [Univ. of Georgia, Athens, GA (United States). Dept. of Biochemistry and Molecular Biology; Arkin, Adam P. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Biological Systems and Engineering Division; Mukhopadhyay, Aindrila [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Biological Systems and Engineering Division; Adams, Michael W. W. [Univ. of Georgia, Athens, GA (United States). Dept. of Biochemistry and Molecular Biology

    2016-12-02

    Cell suspensions of Pelosinus sp. strain UFO1 were previously shown, using spectroscopic analysis, to sequester uranium as U(IV) complexed with carboxyl and phosphoryl group ligands on proteins. The goal of our present study was to characterize the proteins involved in uranium binding. Virtually all of the uranium in UFO1 cells was associated with a heterodimeric protein, which was termed the uranium-binding complex (UBC). The UBC was composed of two S-layer domain proteins encoded by UFO1_4202 and UFO1_4203. Samples of UBC purified from the membrane fraction contained 3.3 U atoms/heterodimer, but significant amounts of phosphate were not detected. The UBC had an estimated molecular mass by gel filtration chromatography of 15 MDa, and it was proposed to contain 150 heterodimers (UFO1_4203 and UFO1_4202) and about 500 uranium atoms. The UBC was also the dominant extracellular protein, but when purified from the growth medium, it contained only 0.3 U atoms/heterodimer. The two genes encoding the UBC were among the most highly expressed genes within the UFO1 genome, and their expressions were unchanged by the presence or absence of uranium. Therefore, the UBC appears to be constitutively expressed and is the first line of defense against uranium, including by secretion into the extracellular medium. Although S-layer proteins were previously shown to bind U(VI), here we showed that U(IV) binds to S-layer proteins, we identified the proteins involved, and we quantitated the amount of uranium bound. Widespread uranium contamination from industrial sources poses hazards to human health and to the environment. Here in this paper, we identified a highly abundant uranium-binding complex (UBC) from Pelosinus sp. strain UFO1. The complex makes up the primary protein component of the S-layer of strain UFO1 and binds 3.3 atoms of U(IV) per heterodimer. Finally, while other bacteria have been shown to bind U(VI) on their S-layer, we demonstrate here an example of U(IV) bound by

  7. Incorporation of europium III complex into nanoparticles and films obtained by the Sol-Gel methodology

    Directory of Open Access Journals (Sweden)

    Faley Jean de Sousa

    2010-03-01

    Full Text Available The sol-gel process is very effective for the preparation of new materials with potential applications in optics, sensors, catalyst supports, coatings, and specialty inorganic polymers that can be used as hosts for the accommodation of organic molecules. The low temperature employed in the process is the main advantage of this methodology. In this work, the europium (III complex with 1,10-phenantroline was prepared, and this luminescent complex was incorporated into silica nanoparticles and films by the sol-gel process. The nanoparticles were obtained by the modified Stöber methodology. The films were obtained by the dip-coating technique, at different deposition rates and numbers of layers. The nanoparticles and films were characterized by photoluminescence, thermal analysis, and Raman and infrared spectroscopies. Characterization revealed that the europium (III complex was not affected upon incorporation into the nanoparticles and films, opening a new field for the application of these materials.

  8. Synthesis and reduction of uranium(V) imido complexes with redox-active substituents

    Energy Technology Data Exchange (ETDEWEB)

    Mullane, Kimberly C.; Carroll, Patrick J.; Schelter, Eric J. [P. Roy and Diana T. Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, PA (United States)

    2017-04-27

    Organic azides that contain naphthyl functional groups were used to prepare uranium(V) imido complexes U{sup V}[=NC(2-naph)Ph{sub 2}][N(SiMe{sub 3}){sub 2}]{sub 3} (2), U{sup V}[=NC(2-naph){sub 3}][N(SiMe{sub 3}){sub 2}]{sub 3} (3), and U{sup V}[=N(2-naph)][N(SiMe{sub 3}){sub 2}]{sub 3} (4), and their properties were compared with U{sup V}[=NCPh{sub 3}][N(SiMe{sub 3}){sub 2}]{sub 3} (1). The electronic structures of these compounds were investigated by solution electrochemistry studies, which revealed accessible U{sup V/VI}, U{sup IV/V}, and naphthalene{sup 0}/naphthalene{sup -1} couples. The uranium(V) naphthylimido complexes were reduced by potassium graphite to yield their uranium(IV) congeners K[U{sup IV}[=NC(2-naph)Ph{sub 2}][N(SiMe{sub 3}){sub 2}]{sub 3}] (2-K), K[U{sup IV}[=NC(2-naph){sub 3}][N(SiMe{sub 3}){sub 2}]{sub 3}] (3-K), and K[U{sup IV}[=N(2-naph)][N(SiMe{sub 3}){sub 2}]{sub 3}] (4-K). The electronic structure of the dianionic compounds were investigated by DFT calculations, and this revealed that the second reduction was ligand-based, which opens the possibility of accomplishing multi-electron redox chemistry by using a tailored multiply-bonded ligand. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  9. Determination of Background Uranium Concentration in the Snake River Plain Aquifer under the Idaho National Engineering and Environmental Laboratory's Radioactive Waste Management Complex

    International Nuclear Information System (INIS)

    Molly K. Leecaster; L. Don Koeppen; Gail L. Olson

    2003-01-01

    Uranium occurs naturally in the environment and is also a contaminant that is disposed of at the Radioactive Waste Management Complex (RWMC) at the Idaho National Engineering and Environmental Laboratory. To determine whether uranium concentrations in the Snake River Plain Aquifer, which underlies the laboratory, are elevated as a result of migration of anthropogenic uranium from the Subsurface Disposal Area in the RWMC, uranium background concentrations are necessary. Guideline values are calculated for total uranium, 234U, 235U, and 238U from analytical results from up to five datasets. Three of the datasets include results of samples analyzed using isotope dilution thermal ionization mass spectrometry (ID-TIMS) and two of the datasets include results obtained using alpha spectrometry. All samples included in the statistical testing were collected from aquifer monitoring wells located within 10 miles of the RWMC. Results from ID-TIMS and alpha spectrometry are combined when the data are not statistically different. Guideline values for total uranium were calculated using four of the datasets, while guideline values for 234U were calculated using only the alpha spectrometry results (2 datasets). Data from all five datasets were used to calculate 238U guideline values. No limit is calculated for 235U because the ID-TIMS results are not useful for comparison with routine monitoring data, and the alpha spectrometry results are too close to the detection limit to be deemed accurate or reliable for calculating a 235U guideline value. All guideline values presented represent the upper 95% coverage 95% confidence tolerance limits for background concentration. If a future monitoring result is above this guideline, then the exceedance will be noted in the quarterly monitoring report and assessed with respect to other aquifer information. The guidelines (tolerance limits) for total U, 234U, and 238U are 2.75 pCi/L, 1.92 pCi/L, and 0.90 pCi/L, respectively

  10. Comparison of Ho and Y complexation data obtained by electromigration methods, potentiometry and spectrophotometry

    International Nuclear Information System (INIS)

    Vinsova, H.; Koudelkova, M.; Ernestova, M.; Jedinakova-Krizova, V.

    2003-01-01

    Many of holmium and yttrium complex compounds of both organic and inorganic origin have been studied recently from the point of view of their radiopharmaceutical behavior. Complexes with Ho-166 and Y-90 can be either directly used as pharmaceutical preparations or they can be applied in a conjugate form with selected monoclonal antibody. Appropriate bifunctional chelation agents are necessary in the latter case for indirect binding of monoclonal antibody and selected radionuclide. Our present study has been focused on the characterization of radionuclide (metal) - ligand interaction using various analytical methods. Electromigration methods (capillary electrophoresis, capillary isotachophoresis), potentiometric titration and spectrophotometry have been tested from the point of view of their potential to determine conditional stability constants of holmium and yttrium complexes. A principle of an isotachophoretic determination of stability constants is based on the linear relation between logarithms of stability constant and a reduction of a zone of complex. For the calculation of thermodynamic constants using potentiometry it was necessary at first to determine the protonation constants of acid. Those were calculated using the computer program LETAGROP Etitr from data obtained by potentiometric acid-base titration. Consequently, the titration curves of holmium and yttrium with studied ligands and protonation constants of corresponding acid were applied for the calculation of metal-ligand stability constants. Spectrophotometric determination of stability constants of selected systems was based on the titration of holmium and yttrium nitrate solutions by Arsenazo III following by the titration of metal-Arsenazo III complex by selected ligand. Data obtained have been evaluated using the computation program OPIUM. Results obtained by all analytical methods tested in this study have been compared. It was found that direct potentiometric titration technique could not be

  11. Communication: Relativistic Fock-space coupled cluster study of small building blocks of larger uranium complexes

    International Nuclear Information System (INIS)

    Tecmer, Paweł; Visscher, Lucas; Severo Pereira Gomes, André; Knecht, Stefan

    2014-01-01

    We present a study of the electronic structure of the [UO 2 ] + , [UO 2 ] 2 + , [UO 2 ] 3 + , NUO, [NUO] + , [NUO] 2 + , [NUN] − , NUN, and [NUN] + molecules with the intermediate Hamiltonian Fock-space coupled cluster method. The accuracy of mean-field approaches based on the eXact-2-Component Hamiltonian to incorporate spin–orbit coupling and Gaunt interactions are compared to results obtained with the Dirac–Coulomb Hamiltonian. Furthermore, we assess the reliability of calculations employing approximate density functionals in describing electronic spectra and quantities useful in rationalizing Uranium (VI) species reactivity (hardness, electronegativity, and electrophilicity)

  12. Communication: Relativistic Fock-space coupled cluster study of small building blocks of larger uranium complexes

    Science.gov (United States)

    Tecmer, Paweł; Severo Pereira Gomes, André; Knecht, Stefan; Visscher, Lucas

    2014-07-01

    We present a study of the electronic structure of the [UO2]+, [UO2]2 +, [UO2]3 +, NUO, [NUO]+, [NUO]2 +, [NUN]-, NUN, and [NUN]+ molecules with the intermediate Hamiltonian Fock-space coupled cluster method. The accuracy of mean-field approaches based on the eXact-2-Component Hamiltonian to incorporate spin-orbit coupling and Gaunt interactions are compared to results obtained with the Dirac-Coulomb Hamiltonian. Furthermore, we assess the reliability of calculations employing approximate density functionals in describing electronic spectra and quantities useful in rationalizing Uranium (VI) species reactivity (hardness, electronegativity, and electrophilicity).

  13. A spectroscopic study of uranium and molybdenum complexation within the pore channels of hybrid mesoporous silica

    Energy Technology Data Exchange (ETDEWEB)

    Charlot, Alexandre [CEA, DEN, DTDC, SPDE, Laboratoire des Procedes Supercritiques de Separation, Bagnols-sur-Ceze (France); CEA, DEN, DTDC, SPDE, Laboratoire de Developpement des Procedes de Separation, Bagnols-sur-Ceze (France); Dumas, Thomas [CEA, DEN, DTDC, SPDE, Laboratoire d' Interaction Ligands Actinides, Bagnols-sur-Ceze (France); Solari, Pier L. [Synchrotron SOLEIL, L' Orme des Merisiers, Saint-Aubin, Gif-sur-Yvette (France); Cuer, Frederic [CEA, DEN, DTDC, SPDE, Laboratoire de Developpement des Procedes de Separation, Bagnols-sur-Ceze (France); Grandjean, Agnes [CEA, DEN, DTDC, SPDE, Laboratoire des Procedes Supercritiques de Separation, Bagnols-sur-Ceze (France)

    2017-01-18

    To enable the reduction of the environmental impact of nuclear energy generation, in this paper, we link the molecular and macroscopic behaviour of a functionalized material (TR rate at SBA15) used to extract uranium from sulfuric media. Two organic 3-[N,N-di(2-ethylhexyl)carbamoyl]-3-[ethoxy(hydroxy)phosphoryl]propanoic acid (TR) molecules grafted onto the solid are involved in the extraction process and form a 2:1 TR-U complex. FTIR and extended X-ray absorption fine structure (EXAFS) spectroscopic analyses show that the TR-U bond is realized through a phosphonate group in a monodentate fashion below pH 3, in agreement with the macroscopic observations. The first coordination sphere of the uranyl ion is completed by two monodentate sulfate ions and one water molecule. Above pH 3, the TR contribution decreases, and other inner-sphere complexes appear, which is consistent with the increased extraction observed on the macroscopic scale. Molybdenum, a competitor element, reduces the uranium extraction capacity but not its speciation, whereas polyoxomolybdates form inside the pores from the molybdenum in solution. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  14. Estimation of rare earth elements in uranium matrix after solvent extraction of uranium as uranium-antipyrine-anion complex using chloroform as solvent

    International Nuclear Information System (INIS)

    Bose, Roopa; Murthy, D.S.R.; Malhotra, R.K.

    1999-01-01

    The neutron economy in a nuclear reactor dictates the occurrence of neutron absorbers at very low levels. Hence the determination of lanthanides especially Sm, Eu, Gd and Dy is one of the most difficult and complicated analytical tasks particularly in high uranium matrix. Solvent extraction is a potent and versatile technique for the separation of lanthanides. The systems generally used for lanthanide extraction are TBP-nitrate, TBP-chloride, TBP-thiocyanate TOPO, DEHPA-nitrate etc. However, these methods of extraction of lanthanides fail to give a clear cut separation for their determination from uranium matrix. Hence analytical procedures have been standardised for extraction of uranium matrix into the organic phase leaving lanthanides unextracted in the aqueous phase. In this direction Cyanex-923 a mixture of 4 trialkyl phosphine oxides, TBP- TOPO and trioctylamine in xylene have been used for extraction of uranium and consequent determination of lanthanides by ICP-AES in the aqueous phase. In this paper the authors have investigated uranium -antipyrine -anion, a different combination other than the well known phosphine oxides and tertiary amines for extraction of uranium

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1958-07-01

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

  16. Trinuclear Schiff base complexes with uranium(V) and copper(II) or zinc(II) ions

    Energy Technology Data Exchange (ETDEWEB)

    Salmon, L.; Thuery, P.; Ephritikhine, M. [CEA Saclay, DSM, DRECAM, Serv Chim Mol, Lab Claude Frejacques, CNRS URA 331, F-91191 Gif Sur Yvette, (France)

    2007-07-01

    Treatment of the uranium(IV) complexes [{l_brace}ML{sup 1}(py){r_brace}{sub 2}U(IV)] (M = Cu, Zn; L{sup 1} = N, N'-bis(3-hydroxy-salicylidene)-1,3-propane-diamine) with silver nitrate in pyridine led to the formation of the corresponding cationic uranium(V) species which were found to be thermally unstable and were converted back into the parent U(IV) complexes; no electron transfer was observed in solution between the U(IV) and U(V) compounds. In the crystals of [{l_brace}ML{sup 1}(py){r_brace}{sub 2}U(IV)][{l_brace}ML{sup 1}(py){r_brace}{sub 2}U(V)][NO{sub 3}], the neutral U(IV) and cationic U(V) species are clearly identified by the distinct U-O distances. Similar reaction of [{l_brace}ZnL{sup 2}(py){r_brace}{sub 2}U(IV)] [L{sup 2} N,N'-bis(3-hydroxy-salicylidene)-1,4-butane-diamine] with AgNO{sub 3} gave crystals of [{l_brace}ZnL{sup 2}(py){r_brace}U(V){l_brace}ZnL{sup 2}(py){sub 2}{r_brace}][NO{sub 3}] but the copper counterpart was not isolated. Crystals of [{l_brace}ZnL{sup 1}(py){r_brace}{sub 2}U(V)][OTf].THF (OTf = OSO{sub 2}CF{sub 3}) were obtained fortuitously from the reaction of [Zn(H{sub 2}L{sup 1})] and U(OTf){sub 3}. (authors)

  17. Radiochemical investigations to the complex formation of uranium (VI) with silicic acid

    International Nuclear Information System (INIS)

    Hrnecek, E.

    1997-12-01

    The complexation of tracer amounts of UO 2 2+ by silicic acid was investigated by an extraction method using 2,5. 10 -3 M 1-(2-thenoyl)-3,3,3-trifloroacetone (IMA) in benzene as extractant at 25 degree C. The tracer used in the experiments was uranium-232, which has been separated from its daughter nuclides by ion exchange from 10 M HCl on Dowex 1x2. The ionic strength in the aqueous phase for the extractions was kept constant at 0,2 M (Na, H)ClO 4 and the pH was varied between pH 2,5 and pH 4,5. For the determination of the stability constants, a silicic acid concentration of 0,01 M, 0,03 M and 0,067 M in the (Na, H)ClO 4 solution was used. The time- and pH- dependence of the polymerization of these silicic acid solutions was determined by kinetical investigations with an ammoniumheptamolybdate-reagent. The uranium concentration in the aqueous and organic phases was determined by liquid scintillation counting using α/β -discrimination. The stability constants determined were log Q1, = -2,20 for the reaction UO 2 2+ Si(OH) 4 = UO 2 OSi(OH) 3 + + H + and Q 2 = -5,87 for the reaction of the polymeric silicate UO 2 2+ (-SiOH) j (-SiOH) j-2 (SiO) 2 UO 2 +2 H + . The influence of silicate on the speciation calculations for uranium in a model natural water is also discussed. (author)

  18. 1. Mono([8]annulene)Uranium(4) half-sandwich complexes, 2. Novel syntheses of symmetrically substituted cyclooctatetetraenes

    International Nuclear Information System (INIS)

    Boussie, T.R.

    1991-10-01

    A reproducible, high-yield synthesis of mono([8]annulene)uranium(4)dichloride (1) is reported, along with the X-ray crystal structural of the bis(pyridine) adduct. Metathesis reactions of the half-sandwich complex 1 with a variety of simple alkyl and alkoxy reagents failed to generate any isolable mono-ring complexes. Reactions of 1 with polydentate, delocalized anions did produce stable derivatives, including mono([8]annulene)uranium(4)bis(acetylacetonate) (4). An X-ray crystal structure of 4 is reported

  19. 1. Mono([8]annulene)Uranium(4) half-sandwich complexes, 2. Novel syntheses of symmetrically substituted cyclooctatetetraenes

    Energy Technology Data Exchange (ETDEWEB)

    Boussie, Thomas Richard [Univ. of California, Berkeley, CA (United States)

    1991-10-01

    A reproducible, high-yield synthesis of mono([8]annulene)uranium(4)dichloride (1) is reported, along with the X-ray crystal structural of the bis(pyridine) adduct. Metathesis reactions of the half-sandwich complex 1 with a variety of simple alkyl and alkoxy reagents failed to generate any isolable mono-ring complexes. Reactions of 1 with polydentate, delocalized anions did produce stable derivatives, including mono([8]annulene)uranium(4)bis(acetylacetonate) (4). An X-ray crystal structure of 4 is reported.

  20. 1. Mono((8)annulene)Uranium(4) half-sandwich complexes, 2. Novel syntheses of symmetrically substituted cyclooctatetetraenes

    Energy Technology Data Exchange (ETDEWEB)

    Boussie, T.R.

    1991-10-01

    A reproducible, high-yield synthesis of mono((8)annulene)uranium(4)dichloride (1) is reported, along with the X-ray crystal structural of the bis(pyridine) adduct. Metathesis reactions of the half-sandwich complex 1 with a variety of simple alkyl and alkoxy reagents failed to generate any isolable mono-ring complexes. Reactions of 1 with polydentate, delocalized anions did produce stable derivatives, including mono((8)annulene)uranium(4)bis(acetylacetonate) (4). An X-ray crystal structure of 4 is reported.

  1. Extraction of Uranium (VI) Nitrate Complexes By Adogen 464. Vol. 3

    International Nuclear Information System (INIS)

    El-Yamani, I.S.; Abd El-Messieh, E.N.

    1996-01-01

    Long-chain amines are frequently used for the extraction of actinides and offer several advantages for their use in the reprocessing of high burn-up nuclear fuels. The present investigation was undertaken to obtain some information on the extraction of Uranium (VI)by adogen 464 from nitrate medium. Extraction parameters studied include: acidity, salting agent, metal and extractant concentrations, diluent type, and temperature. Extraction mechanism was proposed on the basis of results obtained. Best results were attained at 6 M H N O 3 and sodium nitrate was found to increase appreciably the extraction. It was infrared that extraction was dominated by solvation, and ion exchange reaction mechanisms at lower (<6 M) and higher acidities, respectively. As far as diluents are concerned, the dielectric constant, solvation power and donor characteristics were used to explain the variation in the extraction efficiency of the diluents. Kerosene, the most economic particularly when used on industrial scale, was recommended as optimal diluent. Extractability decreases markedly with rise of temperature, suggesting that the extraction behaviour is exothermic; the thermodynamic functions were also calculated and discussed. A method for the separation of uranium (VI) from some fission products existing in high liquid waste was outlined. 3 figs., 2 tabs

  2. Uranium chemistry: significant advances

    International Nuclear Information System (INIS)

    Mazzanti, M.

    2011-01-01

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

  3. Uranium Isotopes as a Tracer of Groundwater Evolution in the Complexe Terminal Aquifer of Southern Tunisia

    Energy Technology Data Exchange (ETDEWEB)

    Hadj Ammar, F. [Laboratory of Radio-Analysis and Environment, National School of Engineering of Sfax, Sfax (Tunisia); Centre Europeen de Recherche et d' Enseignement de Geosciences de l' Environnement, Aix en Provence (France); Deschamps, P.; Hamelin, B. [Centre Europeen de Recherche et d' Enseignement de Geosciences de l' Environnement, Aix en Provence (France); Chkir, N.; Zouari, K. [Laboratory of Radio-Analysis and Environment, National School of Engineering of Sfax, Sfax (Tunisia)

    2013-07-15

    The Complexe Terminal (CT) aquifer system is the main water supply for remote areas of southern Tunisia. Its exploitation has resulted in significant draw-down of the water table. The CT aquifer is a multilayered aquifer lodged in Miocene sand deposits, Senonian limestones and Turonian carbonates. Little is known about the relationships and exchanges between the different layers. Here, uranium isotopic measurements carried out in groundwater samples from the CT aquifer are presented in order to constrain models for mixing of water masses, water-rock interaction and groundwater flow. Analyses were performed using a VG54 (TIMS) at the CEREGE. Results indicate a range in {sup 238}U concentration and {sup 234}U/{sup 238}U activity ratios of 1.5 to 8 ppb and 1.1 to 3.2 respectively. Together with major and trace analyses, uranium isotopic compositions provide important insights into the factors controlling the chemical evolution of groundwater and shows very distinct patterns between carbonate and sandstone layers. (author)

  4. Technological problems concerning the complex recovery of uranium and accompanying elements from sedimentary ores

    International Nuclear Information System (INIS)

    Pinkas, K.

    1977-01-01

    In Poland a deposit of carbonaceous clay shales has been discovered, it contains 1600ppmV, 100ppmu and 180ppm Mo. On the basis of the experiments carried out on the laboratory scale, it has been shown, that the leaching of the shales by means of the diluted solutions of sulphuric acid or sodium carbonates does not assure the high recovery of vanadium and uranium because of their occurrence in shales in refractory forms. The treatment of the shales by using of the concentrated sulphuric acid /250g/1kg shales/, according to the ''acid cure'' method and baking them in the temperature of 250 0 C, has permitted the recovery of 70% vanadium and 65% uranium. From the acid leaching residue, or from the shales directly, 70% of molybdenum can be gained, employing an alkaline pretreatment. The solutions after acid leaching contain great quantities of Al and Fe, which before the separation of U and V by solvent extraction must be to some extent removed. The performed tests have confirmed this, and by using a crystallization process, as by-products the aluminum- and iron sulphates have been obtained. From the solutions, after crystallization by amine solvent extraction, the uranium and vanadium concentrates have been recovered. The currently recognized technological method has been estimated as difficult and expensive. In order to utilize, more economically, this low grade and very refractory for pretreatment shales it is necessary to continue intensive technological research on the improvement of the recognized method and explore new ways, which could contribute to successful solution of this complicated technological problem

  5. Extraction of uranium and lead from mixed waste debris using a variety of metal/ligand complexes

    International Nuclear Information System (INIS)

    Needham, D.A.; Duran, B.L.; Ehler, D.S.; Sauer, N.N.

    1997-01-01

    To ensure the safety of our Nation's nuclear stockpile, Los Alamos National Laboratory is in the process of constructing the DARHT (Dual Axis Radiographic Hydrodynamic Test) facility. DARHT will examine the effects of aging and the stability of our stockpile. Contained testing will be phased in to reduce the impact of these tests, which contain depleted uranium, on our environment. The main focus of this research is to develop a treatment scheme for the recovery of depleted uranium and lead from shot debris that will result from these tests. The goals of this research are to optimize the conditions on a bench scale using a commercially available water soluble polymer to bind the lead and a variety of metal/ligand complexes such as 4,5-dihydroxy-1,3-benzene-disulfonic acid, dithionite, sodium carbonate/bicarbonate, and sodium hypochlorite to bind the uranium. Studies were conducted on a mixture of debris, such as wood, cable, paper towels, and tubing that contained both uranium and lead ranging in concentration from 10-1000's of ppm of contaminants. Experiments were done varying combinations and successions of extractant solutions as well as a number of sequential extractions. Studies show that a mixture of sodium hypochlorite and carbonate removed 90+% of both uranium and lead. We then focused on a separation scheme for the lead and uranium

  6. Decontamination of Uranium-Contaminated Soil Sand Using Supercritical CO2 with a TBP–HNO3 Complex

    Directory of Open Access Journals (Sweden)

    Kwangheon Park

    2015-09-01

    Full Text Available An environmentally friendly decontamination process for uranium-contaminated soil sand is proposed. The process uses supercritical CO2 as the cleaning solvent and a TBP–HNO3 complex as the reagent. Four types of samples (sea sand and coarse, medium, and fine soil sand were artificially contaminated with uranium. The effects of the amount of the reagent, sand type, and elapsed time after the preparation of the samples on decontamination were examined. The extraction ratios of uranium in all of the four types of sand samples were very high when the time that elapsed after preparation was less than a few days. The extraction ratio of uranium decreased in the soil sand with a higher surface area as the elapsed time increased, indicating the possible formation of chemisorbed uranium on the surface of the samples. The solvent of supercritical CO2 seemed to be very effective in the decontamination of soil sand. However, the extraction of chemisorbed uranium in soil sand may need additional processes, such as the application of mechanical vibration and the addition of bond-breaking reagents.

  7. Quantum mechanical calculation of aqueuous uranium complexes: carbonate, phosphate, organic and biomolecular species

    Directory of Open Access Journals (Sweden)

    Jha Prashant

    2009-08-01

    Full Text Available Abstract Background Quantum mechanical calculations were performed on a variety of uranium species representing U(VI, U(V, U(IV, U-carbonates, U-phosphates, U-oxalates, U-catecholates, U-phosphodiesters, U-phosphorylated N-acetyl-glucosamine (NAG, and U-2-Keto-3-doxyoctanoate (KDO with explicit solvation by H2O molecules. These models represent major U species in natural waters and complexes on bacterial surfaces. The model results are compared to observed EXAFS, IR, Raman and NMR spectra. Results Agreement between experiment and theory is acceptable in most cases, and the reasons for discrepancies are discussed. Calculated Gibbs free energies are used to constrain which configurations are most likely to be stable under circumneutral pH conditions. Reduction of U(VI to U(IV is examined for the U-carbonate and U-catechol complexes. Conclusion Results on the potential energy differences between U(V- and U(IV-carbonate complexes suggest that the cause of slower disproportionation in this system is electrostatic repulsion between UO2 [CO3]35- ions that must approach one another to form U(VI and U(IV rather than a change in thermodynamic stability. Calculations on U-catechol species are consistent with the observation that UO22+ can oxidize catechol and form quinone-like species. In addition, outer-sphere complexation is predicted to be the most stable for U-catechol interactions based on calculated energies and comparison to 13C NMR spectra. Outer-sphere complexes (i.e., ion pairs bridged by water molecules are predicted to be comparable in Gibbs free energy to inner-sphere complexes for a model carboxylic acid. Complexation of uranyl to phosphorus-containing groups in extracellular polymeric substances is predicted to favor phosphonate groups, such as that found in phosphorylated NAG, rather than phosphodiesters, such as those in nucleic acids.

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

    International Nuclear Information System (INIS)

    Babenko, S.P.

    2007-01-01

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

  9. Synthesis, characterization, thermogravimetry, and structural study of uranium complexes derived from dibasic S-alkylated thiosemicarbazone ligands

    Czech Academy of Sciences Publication Activity Database

    Fasihizad, A.; Barak, T.; Ahmadi, M.; Dušek, Michal; Pojarová, Michaela

    2014-01-01

    Roč. 67, č. 12 (2014), s. 2160-2170 ISSN 0095-8972 R&D Projects: GA ČR(CZ) GA14-03276S Institutional support: RVO:68378271 Keywords : uranium complex * isothiosemicarbazone * crystallography * spectra * thermal stability Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 2.012, year: 2014

  10. Study of the machining of uranium carbide rods obtained by continuous casting under electronic bombardment; Etude de l'usinage de barreaux de carbure d'uranium obtenus par coulee continue sous bombardement electronique

    Energy Technology Data Exchange (ETDEWEB)

    Rousset, P; Accary, A [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1965-07-01

    The authors consider the various methods of machining uranium mono-carbide and compare them critically in the case of their application to uranium carbide obtained by fusion under an electronic bombardment and continuous casting. This study leads them to propose two mechanical machining methods: cylindrical rectification and center-less rectification, preceded by a preliminary roughing out of a cylinder, the latter appearing more suitable. A study of the machining yields as a function of the diameter of the rough bars and of the diameter of the finished rods has shown that an optimum value of the rough bar diameter exists for each value of the finished rod diameter. It is found that the yield increases as the diameter itself increases, this yield rising from 45 per cent to around 70 per cent as the diameter of the rough bars increases from 25-26 mm to 37-38 mm. (authors) [French] Les auteurs envisagent les differentes methodes d'usinage du monocarbure d'uranium et se livrent a une etude critique de celles-ci, dans le cas de leur application a l'usinage de barreaux de carbure d'uranium obtenus par fusion sous bombardement electronique et coulee continue. Cette etude les conduit a proposer deux methodes d'usinage mecanique: la rectification cylindrique et la rectification 'centerless', precedee d'un ebauchage par carottage, la seconde paraissant la plus appropriee. L'etude des rendements d'usinage en fonction du diametre des barreaux bruts et du diametre des barreaux finis, a mis en evidence une valeur optimale du diametre des barreaux bruts pour chaque valeur du diametre des barreaux usines. Elle a montre que le rendement croit lorsque le diametre croit lui-meme, ce rendement passant d'environ 45 pour cent a environ 70 pour cent, lorsque le diametre des barreaux bruts passe de 25-26 mm a 37-38 mm.

  11. Reversible dihydrogen activation and hydride transfer by a uranium nitride complex

    Energy Technology Data Exchange (ETDEWEB)

    Falcone, Marta; Poon, Lok Nga; Fadaei Tirani, Farzaneh; Mazzanti, Marinella [Institut des Sciences et Ingenierie Chimiques, Ecole Polytechnique Federale de Lausanne (EPFL), Lausanne (Switzerland)

    2018-03-26

    Cleavage of dihydrogen is an important step in the industrial and enzymatic transformation of N{sub 2} into ammonia. The reversible cleavage of dihydrogen was achieved under mild conditions (room temperature and 1 atmosphere of H{sub 2}) by the molecular uranium nitride complex, [Cs{U(OSi(O"tBu)_3)_3}{sub 2}(μ-N)], leading to a rare hydride-imide bridged diuranium(IV) complex, [Cs{U(OSi(O"tBu)_3)_3}{sub 2}(μ-H)(μ-NH)], that slowly releases H{sub 2} under vacuum. This complex is highly reactive and quickly transfers hydride to acetonitrile and carbon dioxide at room temperature, affording the ketimide- and formate-bridged U{sup IV} species [Cs{U(OSi(O"tBu)_3)_3}{sub 2}(μ-NH)(μ-CH{sub 3}CHN)] and [Cs{U(OSi(O"tBu)_3)_3}{sub 2}(μ-HCOO)(μ-NHCOO)]. (copyright 2018 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  12. Study on complexation behaviour of uranium and thorium with amino acids at different temperatures in aqueous media

    International Nuclear Information System (INIS)

    Joshi, J.D.; Patel, M.R.; Patel, A.D.

    1992-01-01

    The complexation behaviour of uranium and thorium with important amino acids have been studied using Irving-Rossotti titration technique at 25deg, 35deg and 45degC in inert atmosphere of nitrogen and 0.1M ionic strength using NaClO 4 . The thermodynamic parameters ΔG, ΔH and ΔS have been calculated. Results indicate that thorium (IV) is forming more stable complexes than UO 2 2+ . (author). 3 refs., 2 tab

  13. Uranium mining during the Cold War. The Wismut plant in the Soviet atomic complex

    International Nuclear Information System (INIS)

    Boch, Rudolf; Karlsch, Rainer

    2011-01-01

    The book on the Wismut plant covers the following issues: Introduction: history of uranium mining of Wismut. Significance of uranium mining in politics and science: Uranium for the strategic equilibrium; the ore of the Cold War; special zones; ''Party within the Party'', radiation protection in uranium mining; Freiberg's geoscientists searching strategic metals in the 1940ies; end of the shift. Social history and daily routine: Good money for hard work; foreign among ''friends''; personnel data; gainful employment for women and emancipation in the frame of mining; from symphony orchestra to laymen circles; the fightning spirit of pitman-sportsmen.

  14. Luminescent hybrid films obtained by covalent grafting of terbium complex to silica network

    International Nuclear Information System (INIS)

    Liu Fengyi; Fu Lianshe; Wang Jun; Liu Ze; Li Huanrong; Zhang Hongjie

    2002-01-01

    Luminescent hybrid thin films consisting of terbium complex covalently bonded to a silica-based network have been obtained in situ via a sol-gel approach. A new monomer, N-(4-benzoic acid-yl), N'-(propyltriethoxysilyl)urea (PABI), has been synthesized by grafting isocyanatopropyltriethoxysilane (ICPTES) to p-aminobenzoic acid and characterized by 1 H NMR, IR and MS. The monomer acts as a ligand for Tb 3+ ion and as a sol-gel precursor. Band emission from Tb 3+ ion due to an efficient ligand-to-metal energy transfer was observed by UV excitation. The decay curves of Tb 3+ in the hybrid films were measured. The energy difference between the triplet state energy of PABI and the 5 D 4 level of Tb 3+ ion falls in the exciting range to sensitize Tb 3+ ion fluorescence

  15. Chromatographic retention of molybdenum, titanium and uranium complexes for removal of some interferences in inductively-coupled plasma mass spectrometry

    International Nuclear Information System (INIS)

    Jiang, S.-J.; Palmieri, M.D.; Fritz, J.S.; Houk, R.S.; Iowa State Univ., of Science and Technology, Ames

    1987-01-01

    Complexes of molybdenum(VI) or titanium(IV) with N-methylfurohydroxamic acid (N-MFHA) are retained on a column packed with polystyrene/divinylbenzene. At the pH values chosen, copper, zinc and cadmium are washed rapidly through the column and are detected by inductively-coupled plasma mass spectrometry without interference from metal oxide ions of titanium or molybdenum. Detection limits are 1 to 2 μg l -1 , and analyte recoveries are essentially 100%. The resin capacity for the titanium and molybdenum complexes is sufficient for several hundred injections, and the complexes can be readily washed from the column. Uranium(VI) also forms a stable complex with N-MFHA, and ionization interference caused by excess of uranium can be avoided by chromatographic removal of the uranium complex. Various other potentially interfering elements with aqueous oxidation states of +4 or higher (e.g. Sn, W, Hf or Zr) could also be separated by this technique. 33 refs.; 4 figs.; 3 tabs

  16. Uranium mining

    International Nuclear Information System (INIS)

    Lange, G.

    1975-01-01

    The winning of uranium ore is the first stage of the fuel cycle. The whole complex of questions to be considered when evaluating the profitability of an ore mine is shortly outlined, and the possible mining techniques are described. Some data on uranium mining in the western world are also given. (RB) [de

  17. Activation of the C-H bond: catalytic hydroxylation of hydrocarbons by new cobaltic alkylperoxydic complexes; selective and catalytic cycloalkane dehydrogenation in presence of uranium for hydrogen transfer

    International Nuclear Information System (INIS)

    Brazi, E.

    1987-01-01

    The aim of the thesis is to improve efficiency and selectivity of chemical reactions for alkane transformations. In the first part decomposition of hydroperoxides and hydrocarbon hydroxylation by cobalt complexes is studied. In the second part cycloalkanes are dehydrogenated into aromatics with a Pt catalyst, trapping hydrogen by uranium. Uranium hydride UH 3 can yield very pure hydrogen at reasonable temperature [fr

  18. Study of electrochemical properties of the Prussian blue obtained via pentacyanidoferrate complex

    Energy Technology Data Exchange (ETDEWEB)

    Monteiro, Marcio Cristiano; Toledo, Kalil Cristhian Figueiredo; Pires, Bruno Morandi; Bonacin, Juliano Alves, E-mail: monteiromarcioc@gmail.com [Universidade Estadual de Campinas (UNICAMP), SP (Brazil). Instituto de Quimica; Wick, Rene [University of Zurich (Switzerland)

    2016-07-01

    Full text: Prussian blue (PB) is one the most important compounds used in electrochemical sensing of molecular targets as H{sub 2}O{sub 2}. Many diseases or biochemical abnormalities can be diagnosed by analysis of H{sub 2}O{sub 2}. The properties found in PB comes from the electronic structure of this material which is formed by Fe{sup 2+} bonded to iron Fe{sup 3+} by cyanide bridged arranged in a 3D structure. Furthermore, the intervalence observed allows to achieve different levels of oxidation in the same process[1]. The challenge in this area is how to control and modulate specific features of PB. Because of this, we are interested in evaluating how the ligand Nmethylpyrazinium affects the structure and reactivity of the N-methylpyraziniumpentacyanidoferrate(II)(PCF) and its PB corresponding. According to XRD, the PB obtained from PCF produces an amorphous structure instead of the highly ordered structure of PB obtained by classical methods. The stoichiometry of formation of the PB(classic) obtained by the Job's method is 1: 1 (Fe(III): [Fe(CN){sub 6}]{sup 4-}), on the other hand, in PB-PCF the stoichiometry is 1: 2 (Fe(III):PCF). The reported features cause differences in the oxidation potential of the films, PB(classic) Eox=0.167V and PB-PCF Eox=0.219V. In terms of sensing of H{sub 2}O{sub 2}, the PB(classic) presented LOD= 1.2 10{sup -4} M and PB-mpz LOD= 5.8 10{sup -5}M. We have concluded that different sources of iron complexes cause alterations in the organization and electronic structure of the PB. Reference: [1] B. M. Pires, S. A. V. Jannuzzi, A. L. B. Formiga, J. A. Bonacin, Eur J Inorg Chem, 5812, (2014). (author)

  19. Complexation of vanadium with amidoxime and carboxyl groups. Uncovering the competitive role of vanadium in uranium extraction from seawater

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Cong-Zhi; Wu, Qun-Yan; Lan, Jian-Hui; Shi, Wei-Qun [Chinese Academy of Sciences, Beijing (China). Inst. of High Energy Physics; Chai, Zhi-Fang [Chinese Academy of Sciences, Beijing (China). Inst. of High Energy Physics; Soochow Univ., Suzhou (China). School of Radiological and Interdisciplinary Sciences (RAD-X); Wu, Guo-Zhong [Chinese Academy of Sciences, Shanghai (China). Shanghai Inst. of Applied Physics

    2017-09-01

    At present, amidoxime-based adsorbents are considered to be the most promising materials for extraction of uranium from seawater. However, the high concentrations of transition metals especially vanadium strongly compete with uranium in the sequestration process, which is extremely limited the commercial use of amidoxime-based adsorbents. In this work, the coordination modes, bonding nature, and stabilities of possible vanadium(IV) (VO{sup 2+}) and (V) (VO{sub 2}{sup +}, VO{sup 3+}, V{sup 5+}) complexes with amidoximate (AO{sup -}), carboxyl (Ac{sup -}), glutarimidedioximate (HA{sup -}) and deprotonated glutarimidedioximate (A{sup 2-}) on single and double alkyl chains (R=C{sub 13}H{sub 26}) are systematically explored by quantum chemical calculations. Different from the uranyl (UO{sub 2}{sup 2+}) complexes, the AO{sup -} groups of the vanadium(IV) and (V) complexes prefer to coordinate as monodentate and chelate ligands, while few species with AO{sup -} groups in η{sup 2}-binding mode have been observed in the vanadium complexes. Besides, the vanadium complexes are predicted to have obvious covalent metal-ligand bonds. According to thermodynamic stability analysis, all the vanadium complexes with AO{sup -}, Ac{sup -}, HA{sup -} and A{sup 2-} ligands on double alkyl chains are found to be more stable than corresponding complexes with ligands on a single chain. The synergistic effect of the amidoxime and carboxyl groups can be observed in most of VO{sub 2}{sup +} and VO{sup 3+} complexes with mixed ligands (AO{sup -}/Ac{sup -}). The vanadium(IV) and (V) complexes are more stable than the corresponding uranyl complexes, and the adsorption capability of the amidoxime-based adsorbents toward vanadium(V) ions decrease in the order of VO{sub 2}{sup +}>VO{sup 3+}> V{sup 5+}. The dioxovanadium cation VO{sub 2}{sup +} is predicted to form multinuclear vanadium complex in the sequestration process, possibly resulting in higher stable VO{sub 2}{sup +} complexes. Therefore

  20. On the influence of infiltration of radioactive beds by flushing fluid on γ-ray logging results obtained from uranium deposit No. 387

    International Nuclear Information System (INIS)

    Ren Bingxiang; Zhang Yuechun; Ai Shuyi.

    1985-01-01

    A large number of field logging data obtained during the course of exploration on uranium deposit No. 387 show when the radioactive beds are encountered by drill holes and the drilling continues the γ-ray intensity decreases. It is considered that the escape of emanation does not considerably influence the logging results. Therefore, based upon the experiment of immerseing ores in fluid and geological and hydrogeological data of the deposit, the hypotheses that the γ-ray intensity in drill hole is closely related with the infiltration of flushing fluid is suggested. The ore bodies are strictly controlled by faults. Most of the uranium and thorium are absorbed by pelitic-carbonaceous cements or fill the porous spaces in structural breccia and cataclasite. They are easy to dissolve in water. Moreover, the ore-bearing structures are the unique water aquifers which is under pressure. As the level of flushing fluid is higher than the pressure head so it continuously pours into the ore-bearing beds, resulting in the infiltration of U and Ra. Consequently, the radioactivity detected is low

  1. Adsorption of uranium(VI) to manganese oxides: X-ray absorption spectroscopy and surface complexation modeling.

    Science.gov (United States)

    Wang, Zimeng; Lee, Sung-Woo; Catalano, Jeffrey G; Lezama-Pacheco, Juan S; Bargar, John R; Tebo, Bradley M; Giammar, Daniel E

    2013-01-15

    The mobility of hexavalent uranium in soil and groundwater is strongly governed by adsorption to mineral surfaces. As strong naturally occurring adsorbents, manganese oxides may significantly influence the fate and transport of uranium. Models for U(VI) adsorption over a broad range of chemical conditions can improve predictive capabilities for uranium transport in the subsurface. This study integrated batch experiments of U(VI) adsorption to synthetic and biogenic MnO(2), surface complexation modeling, ζ-potential analysis, and molecular-scale characterization of adsorbed U(VI) with extended X-ray absorption fine structure (EXAFS) spectroscopy. The surface complexation model included inner-sphere monodentate and bidentate surface complexes and a ternary uranyl-carbonato surface complex, which was consistent with the EXAFS analysis. The model could successfully simulate adsorption results over a broad range of pH and dissolved inorganic carbon concentrations. U(VI) adsorption to synthetic δ-MnO(2) appears to be stronger than to biogenic MnO(2), and the differences in adsorption affinity and capacity are not associated with any substantial difference in U(VI) coordination.

  2. Study of the machining of uranium carbide rods obtained by continuous casting under electronic bombardment; Etude de l'usinage de barreaux de carbure d'uranium obtenus par coulee continue sous bombardement electronique

    Energy Technology Data Exchange (ETDEWEB)

    Rousset, P.; Accary, A. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1965-07-01

    The authors consider the various methods of machining uranium mono-carbide and compare them critically in the case of their application to uranium carbide obtained by fusion under an electronic bombardment and continuous casting. This study leads them to propose two mechanical machining methods: cylindrical rectification and center-less rectification, preceded by a preliminary roughing out of a cylinder, the latter appearing more suitable. A study of the machining yields as a function of the diameter of the rough bars and of the diameter of the finished rods has shown that an optimum value of the rough bar diameter exists for each value of the finished rod diameter. It is found that the yield increases as the diameter itself increases, this yield rising from 45 per cent to around 70 per cent as the diameter of the rough bars increases from 25-26 mm to 37-38 mm. (authors) [French] Les auteurs envisagent les differentes methodes d'usinage du monocarbure d'uranium et se livrent a une etude critique de celles-ci, dans le cas de leur application a l'usinage de barreaux de carbure d'uranium obtenus par fusion sous bombardement electronique et coulee continue. Cette etude les conduit a proposer deux methodes d'usinage mecanique: la rectification cylindrique et la rectification 'centerless', precedee d'un ebauchage par carottage, la seconde paraissant la plus appropriee. L'etude des rendements d'usinage en fonction du diametre des barreaux bruts et du diametre des barreaux finis, a mis en evidence une valeur optimale du diametre des barreaux bruts pour chaque valeur du diametre des barreaux usines. Elle a montre que le rendement croit lorsque le diametre croit lui-meme, ce rendement passant d'environ 45 pour cent a environ 70 pour cent, lorsque le diametre des barreaux bruts passe de 25-26 mm a 37-38 mm.

  3. Portsmouth Uranium Enrichment Complex environmental monitoring report for calendar year 1984

    International Nuclear Information System (INIS)

    1985-05-01

    At the Portsmouth Uranium Enrichment Complex all effluent streams are sampled regularly and analyzed to assess compliance with applicable environmental standards. Radioactivity is measured in air, water, fish, produce, soil, and sediments; and radiation doses to the public are calculated. The calculated public radiation doses from process effluents are within US Department of Energy (DOE) and US Environmental Protection Agency standards. An extensive amount of engineering effort is underway to modify existing airborne radioactivity emissions sources to further reduce emissions in compliance with DOE policy. Non-radioactive effluents either presently comply with federal standards or will comply upon completion of planned projects. CY-1984 was the fourth full year under the current National Pollutant Discharge Elimination System (NPDES) permit for liquid effluents, and the second year the Ohio Environmental Protection Agency (EPA) assumed responsibility for administering the NPDES program. Compliance with the permit's discharge limits, with the exception of violations due to the startup of two new wastewater treatment facilities, did not present any significant problems. Overall compliance was 94.7%

  4. Portsmouth Uranium Enrichment Complex environmental monitoring report for calendar year 1985

    International Nuclear Information System (INIS)

    1986-05-01

    At the Portsmouth Uranium Enrichment Complex all effluent streams are sampled regularly and analyzed to assess compliance with applicable environmental standards. Radioactivity is measured in air, water, fish, produce, soil, sediments and vegetation; and radiation doses to the public are calculated. The calculated public radiation doses from process effluents are within US Department of Energy (DOE) and US Environmental protection Agency (USEPA) standards. An extensive amount of engineering effort is underway to modify existing airborne radioactivity emissions sources to further reduce emissions in compliance with DOE policy. Non-radioactive effluents either presently comply with federal standards or will comply upon completion of planned projects. CY-1985 was the fifth full year under the current National Pullutant Discharge Elimination System (NPDES) permit for liquid effluents, and the third year since the Ohio Environmental Protection Agency (OEPA) assumed responsibility for administering the NPDES program. Compliance with the permit's discharge limits, with the exception of violations due to the Coal Pile Treatment Facility and the Biodenitrification Plant for which projects to improve performance are currently underway, did not present any significant problems. Overall compliance was 95.5%. There was increased activity in the areas of groundwater monitoring, hazardous waste and PCB waste management to comply with Federal regulations

  5. Geochemistry of the uranium mineralized Achala granitic complex, Argentina: Comparison with Hercynian peraluminous leucogranites of western Europe

    International Nuclear Information System (INIS)

    Cuney, M.; Leroy, J.; Valdiviezo, P.A.; Daziano, C.; Gamba, M.; Zarco, A.J.; Morello, O.; Ninci, C.; Molina, P.

    1989-01-01

    The Achala granitic complex belongs to the Sierras Pampeanas Hercynian belt, located west of the city of Cordoba, Argentina. This complex is very large (about 100 km N-S and 40 km E-W) and is composed of biotite, biotite with muscovite and muscovite with tourmaline granites intruded in amphibolite grade metamorphic rocks, along a main N 20 deg. E structural direction. Numerous uranium mineralizations are located within the granitic massif and tungsten mineralizations are present both in the enclosing metamorphic rocks and in the granite. The geochemistry of the granite has been studied in four test areas (Southern, Copina, Median and Don Vincente). Two test areas (Median and Don Vicente) present clear evidence of hydrothermal alteration: albitization and dequartzification similar to the French 'episyenites', silicification and argillic alteration. Potassic alteration is rare and weakly developed. The two test areas with hydrothermal alteration present a high uranium geochemical background (5-30 ppm). High thorium contents (up to 65 ppm) are essentially observed in the less differentiated granites of the Copina and Median areas. Thorium/uranium ratios are highly variable (1-10). Uranium minerals are related to different environments - (1) apatite-biotite enclave mineralized with uraninite and uranothorite, (2) gneiss from the contact metamorphism rim, (3) granite with incipient dequartzification, (4) granite associated with albitic episyenites and (5) silicified granite - but are all located in the two test areas presenting clear evidence of hydrothermal alteration. The three petrogenetic events are clearly related to very different mechanisms, separated from each other by several tens of millions of years in the west European Hercynian chain. In the same period the same succession of events leading to uranium deposits is observed in Argentina. 34 refs, 10 figs, 1 tab

  6. Uranium exploration target selection for proterozoic iron oxide/breccia complex type deposits in India

    International Nuclear Information System (INIS)

    Dwivedy, K.K.; Sinha, K.K.

    1997-01-01

    Multimetal iron oxide/breccia complex (IOBC) type deposits exemplified by Olympic Dam in Australia, fall under low grade, large tonnage deposits. A multidisciplinary integrated exploration programme consisting of airborne surveys, ground geological surveys, geophysical and geochemical investigations and exploratory drilling, supported adequately by the state of the art analytical facilities, data processing using various software and digital image processing has shown moderate success in the identification of target areas for this type of deposits in the Proterozoic terrains of India. Intracratonic, anorogenic, continental rift to continental margin environment have been identified in a very wide spectrum of rock associations. The genesis and evolution of such associations during the Middle Proterozoic period have been reviewed and applied for target selection in the (i) Son-Narmada rift valley zone; (ii) areas covered by Dongargarh Supergroup of rocks in Madhya Pradesh; (iii) areas exposing ferruginous breccia in the western part of the Singhbhum Shear Zone (SSZ) around Lotapahar; (iv) Siang Group of rocks in Arunachal Pradesh; (v) Crystalline rocks of Garo Hills around Anek; and (vi) Chhotanagpur Gneissic complex in the Bahia-Ulatutoli tract of Ranchi Plateau. Of theses six areas, the Son-Narmada rift area appears to be the most promising area for IOBC type deposits. Considering occurrences of the uranium anomalies near Meraraich, Kundabhati, Naktu and Kudar and positive favourability criteria observed in a wide variety of rocks spatially related to the rifts and shears, certain sectors in Son-Narmada rift zone have been identified as promising for intense subsurface exploration. 20 refs, 4 figs, 1 tab

  7. Environmental management plan of the mining and industrial uranium complex in Brazil

    International Nuclear Information System (INIS)

    Figuereido, N.; Hilton, M.; Wiikman, L.; Oliveira, M.; Taddei, J.

    1996-01-01

    The Mining and Industrial Complex of the Pocos de Caldas Plateau (CIPC) is located at Caldas, county in the southwest of Minas Gerais state. It is a plant of the Industrias Nucleares do Brazil S.A. -INB, the only installation in Brazil for the production of uranium concentrate (yellow-cake) as ammonium diuranate (Adu). The Environmental protection and control program in practice assures the environmental management plan, in operation, maintaining the Complex within technology standards required by updated environmental concepts. The mine is an open pit operation with a surface diameter of 1000 m and an actual average depth of 120 m. Some 44 x 10 6 m 3 of the overburden material were used in embankments structures to civil engineering works in the implantation of several installations in CIPC, and the other portion of the removed material was deposited in two pre-selected areas having both an upper area of about 2,0 x 10 6 m 2 . The annual average volume of waters transported to chemical treatment is about 9,0 x 10 5 m 3 . The mill, in its full operation, processes 2500 t of ore per day and the solid and liquid tailings are directed to a waste pond system where are contained approximately 2,0 x 10 6 m 3 (2,2 x 10 6 t) of solid wastes with an estimation of further 70 x 10 5 m 3 to be disposed. The upper surface of tailings pond is about 2,0 x 10 5 m 2 . Nowadays, the environmental protection and control program aims to the development of potential pollutant areas stabilization reintegrating them into their original features or adjusting them to other forms of laudable restoration. (authors). 1 fig

  8. Synthesis and studies of novel high metal content organic aerogels obtained from a polymerizable titanium complex

    International Nuclear Information System (INIS)

    Cadra, S.

    2010-01-01

    Inertial Confinement Fusion (ICF) is a technique widely studied by the French atomic commission (CEA). Experiments will be performed within the Laser Megajoule (LMJ). They require innovative materials like organic aerogels that constitute laser targets. Such polymeric material must provide both a high porosity and a significant titanium percentage (1 atom %). Moreover, the monomers developed must be compatible with the synthesis procedure already in use. According to these specifications, a new polymerizable titanium complex was synthesized and fully characterized. This air and moisture-stable monomer provides a high metal percentage. Its free-radical cross-linked copolymerization affords several titanium-containing polymers. These gels were dried under supercritical conditions and organic aerogels were obtained. The chemical compositions of these materials were investigated by NMR, IR and elemental analysis while their structure was characterized by MEB-EDS, MET, N 2 adsorption/desorption isotherms measurements and SAXS. The data collected fit the specification requirements. Moreover, the mechanisms responsible of the foam nano-structure formation were discussed. (author) [fr

  9. Complex-shaped ceramic composites obtained by machining compact polymer-filler mixtures

    Directory of Open Access Journals (Sweden)

    Rosa Maria da Rocha

    2005-06-01

    Full Text Available Research in the preparation of ceramics from polymeric precursors is giving rise to increased interest in ceramic technology because it allows the use of several promising polymer forming techniques. In this work ceramic composite pieces were obtained by pyrolysis of a compacted mixture of a polysiloxane resin and alumina/silicon powder. The mixture consists of 60 vol% of the polymer phase and 40 vol% of the filler in a 1:1 ratio for alumina/silicon, which was hot pressed to crosslink the polymer, thus forming a compact body. This green body was trimmed into different geometries and pyrolised in nitrogen atmosphere at temperatures up to 1600 °C. X-ray diffraction analysis indicated the formation of phases such as mullite and Si2ON2 during pyrolysis, that result from reactions between fillers, polymer decomposition products and nitrogen atmosphere. The porosity was found to be less than 20% and the mass loss around 10%. The complex geometry was maintained after pyrolysis and shrinkage was approximately 8%, proving pyrolisis to be a suitable process to form near-net-shaped bulk ceramic components.

  10. Tetra- and hexavalent uranium forms bidentate-mononuclear complexes with particulate organic matter in a naturally uranium-enriched peatland

    DEFF Research Database (Denmark)

    Mikutta, Christian; Langner, Peggy; Bargar, John R.

    2016-01-01

    Peatlands frequently serve as efficient biogeochemical traps for U. Mechanisms of U immobilization in these organic matter-dominated environments may encompass the precipitation of U-bearing mineral(oid)s and the complexation of U by a vast range of (in)organic surfaces. The objective of this work...... of bidentate-mononuclear U(IV/VI) complexes with carboxyl groups. We neither found evidence for U shells at ∼3.9 Å, indicative of mineral-associated U or multinuclear U(IV) species, nor for a substantial P/Fe coordination of U. Our data indicates that U(IV/VI) complexation by natural organic matter prevents...... the precipitation of U minerals as well as U complexation by Fe/Mn phases at our field site, and suggests that organically complexed U(IV) is formed via reduction of organic matter-bound U(VI)....

  11. Uranium Conversion & Enrichment

    Energy Technology Data Exchange (ETDEWEB)

    Karpius, Peter Joseph [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2017-02-06

    The isotopes of uranium that are found in nature, and hence in ‘fresh’ Yellowcake’, are not in relative proportions that are suitable for power or weapons applications. The goal of conversion then is to transform the U3O8 yellowcake into UF6. Conversion and enrichment of uranium is usually required to obtain material with enough 235U to be usable as fuel in a reactor or weapon. The cost, size, and complexity of practical conversion and enrichment facilities aid in nonproliferation by design.

  12. Method of preparation of uranium nitride

    Science.gov (United States)

    Kiplinger, Jaqueline Loetsch; Thomson, Robert Kenneth James

    2013-07-09

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

  13. Complexes of uranium tetrachlorides and thorium tetrachloride with N-methylpiperazine, 2-methylpiperazine, N-phenylpiperazine, N,N'-dimethylpiperazine and pyrazine

    Energy Technology Data Exchange (ETDEWEB)

    Manhas, B S; Trikha, A K [Punjabi Univ., Patiala (India). Dept. of Chemistry; Singh, M

    1979-01-01

    Stable complexes of uranium tetrachloride and thorium tetrachloride with the title ligands have been synthesised and characterised on the basis of elemental analyses, IR and electronic reflectance spectral studies and magnetic susceptibility measurements. The ligands probably coordinate in the chair conformation bridging the metal ions as indicated by IR spectral studies and insolubility of these complexes in common organic solvents. A coordination number of six for uranium (IV) is suggested by the electronic reflectance spectral and magnetic susceptibility data.

  14. Multisensor system for determination of iron(II), iron(III), uranium(VI) and uranium(IV) in complex solutions

    International Nuclear Information System (INIS)

    Legin, A.V.; Seleznev, B.L.; Rudnitskaya, A.M.; Vlasov, Yu.G.; Tverdokhlebov, S.V.; Mack, B.; Abraham, A.; Arnold, T.; Baraniak, L.; Nitsche, H.

    1999-01-01

    Development and analytical evaluation of a multisensor system based on the principles of 'electronic tongue' for the determination of low contents of uranium(VI), uranium(IV), iron(II) and iron(III) in complex aqueous media have been carried out. A set of 29 different chemical sensors on the basis of all- solid-state crystalline and vitreous materials with enhanced electronic conductivity and redox and ionic cross-sensitivity have been incorporated into the sensor array. Multidimensional data have been processed by pattern recognition methods such as artificial neural networks and partial least squares. It has been demonstrated that Fe(II) and Fe(III) contents in the range from 10 -7 to 10 -4 mol L -1 of total iron concentration can be determined with the average precision of about 25 %. U(VI) and U(IV) contents can been determined with the average precision of 10-40% depending on the concentration. The developed multisensor system can be applied in future for the analysis of mining and borehole waters as well other contaminated natural media, including on-site measurements. (author)

  15. Technical Basis For Radiological Acceptance Criteria For Uranium At The Y-12 National Security Complex

    Energy Technology Data Exchange (ETDEWEB)

    Veinot, K. G.

    2009-07-22

    The purpose of this report is to establish radiological acceptance criteria for uranium. Other factors for acceptance not considered include criticality safety concerns, contaminants to the process stream, and impacts to the Safety Basis for the affected facilities. Three types of criteria were developed in this report. They include limits on external penetrating and non-penetrating radiation and on the internal hazard associated with inhalation of the material. These criteria are intended to alleviate the need for any special controls beyond what are normally utilized for worker protection from uranium hazards. Any proposed exceptions would require case-by-case evaluations to determine cost impacts and feasibility. Since Y-12 has set rigorous ALARA goals for worker doses, the external limits are based on assumptions of work time involved in the movement of accepted material plus the desire that external doses normally received are not exceeded, and set so that no special personnel monitoring would be required. Internal hazard controls were established so that dose contributions from non-uranium nuclides would not exceed 10% of that expected from the uranium component. This was performed using a Hazard Index (HI) previously established for work in areas contaminated with non-uranium nuclides. The radiological acceptance criteria for uranium are summarized in Table 1. Note that these limits are based on the assumption that radioactive daughter products have reached equilibrium.

  16. Solution of environmental protection problems and complex utilization of raw materials during mining and processing of uranium ores

    International Nuclear Information System (INIS)

    Litvinenko, V.G.; Savva, P.P.

    1993-01-01

    Consideration is given to the complex of measures taken in Priargunsky industrial mine-chemical association and directed to environment protection, complex utilization of raw materials during mining and processing of uranium ores. These measures include: 1) reduction of toxic chemical agent effluents into atmosphere due to introduction of new methods and gas cleaning systems; 2) rational use of water resources owing to application of circulating water supply systems, waste waters treatment and effective control of the state of water consumption by industrial enterprises; 3) utilization of gangue and industrial solid wastes

  17. Approaches to surface complexation modeling of Uranium(VI) adsorption on aquifer sediments

    Science.gov (United States)

    Davis, J.A.; Meece, D.E.; Kohler, M.; Curtis, G.P.

    2004-01-01

    Uranium(VI) adsorption onto aquifer sediments was studied in batch experiments as a function of pH and U(VI) and dissolved carbonate concentrations in artificial groundwater solutions. The sediments were collected from an alluvial aquifer at a location upgradient of contamination from a former uranium mill operation at Naturita, Colorado (USA). The ranges of aqueous chemical conditions used in the U(VI) adsorption experiments (pH 6.9 to 7.9; U(VI) concentration 2.5 ?? 10-8 to 1 ?? 10-5 M; partial pressure of carbon dioxide gas 0.05 to 6.8%) were based on the spatial variation in chemical conditions observed in 1999-2000 in the Naturita alluvial aquifer. The major minerals in the sediments were quartz, feldspars, and calcite, with minor amounts of magnetite and clay minerals. Quartz grains commonly exhibited coatings that were greater than 10 nm in thickness and composed of an illite-smectite clay with occluded ferrihydrite and goethite nanoparticles. Chemical extractions of quartz grains removed from the sediments were used to estimate the masses of iron and aluminum present in the coatings. Various surface complexation modeling approaches were compared in terms of the ability to describe the U(VI) experimental data and the data requirements for model application to the sediments. Published models for U(VI) adsorption on reference minerals were applied to predict U(VI) adsorption based on assumptions about the sediment surface composition and physical properties (e.g., surface area and electrical double layer). Predictions from these models were highly variable, with results overpredicting or underpredicting the experimental data, depending on the assumptions used to apply the model. Although the models for reference minerals are supported by detailed experimental studies (and in ideal cases, surface spectroscopy), the results suggest that errors are caused in applying the models directly to the sediments by uncertain knowledge of: 1) the proportion and types of

  18. Copolymers containing phosphorescent iridium(III) complexes obtained by free and controlled radical polymerization techniques

    NARCIS (Netherlands)

    Ulbricht, C.; Becer, C.R.; Winter, A.; Veldman, D.; Schubert, U.S.

    2008-01-01

    A methacrylate-functionalized phosphorescent Ir(III)-complex has been synthesized, characterized, and applied as a monomer in radical copolymerizations. Together with methyl methacrylate, the complex has been copolymerized under free radical polymerization conditions. Aiming for host-guest-systems,

  19. Zircon U-Pb geochronology and geochemistry of granites in the Zhuguangshan complex, South China: Implications for uranium mineralization

    Science.gov (United States)

    Zhang, Long; Chen, Zhenyu; Li, Xiaofeng; Li, Shengrong; Santosh, M.; Huang, Guolong

    2018-05-01

    The Zhuguangshan complex, composed of Caledonian, Indosinian, and Yanshanian granites, and Cretaceous mafic dykes, is one of the most important granite-hosted uranium producers in South China. Here we present LA-ICP-MS zircon U-Pb and hornblende 40Ar/39Ar geochronology and whole-rock and biotite geochemistry for the granites in this complex to evaluate the magmatism and its constraints on uranium mineralization. Samples collected from the Fuxi, Youdong, Longhuashan, Chikeng, Qiling, and Sanjiangkou intrusions yield zircon weighted 206Pb/238U ages of 426.7 ± 5.4 Ma, 226.4 ± 3.5 Ma, 225.0 ± 2.7 Ma, 152.2 ± 3.0 Ma, 153.9 ± 2.1 Ma, and 155.2 ± 2.1 Ma, respectively. A new Ar-Ar dating of the hornblende of the diabase from the Changjiang uranium ore field yields a plateau age of 145.1 ± 1.5 Ma. These results coupled with published geochronological data indicate that six major magmatic events occurred in the study area at 420-435 Ma, 225-240 Ma, 150-165 Ma, 140 Ma, 105 Ma, and 90 Ma. Both U-bearing and barren granites occur in this complex, and they display differences in whole-rock and biotite geochemistry. The barren granites show higher Al2O3, CaO, TFMM, Rb, Zr, Ba, SI, Mg#, (La/Yb)N, and Eu/Eu*, but lower SiO2, ALK, Rb, DI, Rb/Sr, and TiO2/MgO than those of the U-bearing granites. Biotites in the U-bearing granites are close to the Fe-rich siderophyllite-annite end member with Fe/(Fe + Mg) ratios higher than 0.66, whereas those in the barren granites are relatively close to the Mg-rich eastonite-phlogopite end member with Fe/(Fe + Mg) ratios uranium ore potential of the granites in the Zhuguangshan complex. The geochemical variations of U-bearing and barren granites can serve as a potential detector for granite-hosted uranium deposits.

  20. Final Report - Elucidating Bioreductive Transformations within Physically Complex Media: Impact on the Fate and Transport of Uranium and Chromium

    International Nuclear Information System (INIS)

    Benner, Shawn G.; Fendorf, Scott

    2009-01-01

    In situ stabilization (inclusive of natural attenuation) of toxic metals and radionuclides is an attractive approach for remediating many contaminated DOE sites. By immobilizing toxic metals and radionuclides in place, the removal of contaminated water to the surface for treatment as well as the associated disposal costs are avoided. To enhance in situ remediaton, microbiological reductive stabilization of contaminant metals has been, and continues to be, actively explored. It is likely that surface and subsurface microbial activity can alter the redox state of toxic metals and radionuclides, either directly or indirectly, so they are rendered immobile. Furthermore, anaerobic bacterial metabolic products will help to buffer pulses of oxidation, typically from fluxes of nitrate or molecular oxygen, and thus may stabilize reduced contaminants from oxidative mobilization. Uranium and chromium are two elements of particular concern within the DOE complex that, owing to their abundance and toxicity, appear well suited for biologically mediated reductive stabilization. Subsurface microbial activity can alter the redox state of toxic metals and radionuclides, rending them immobile. Imparting an important criterion on the probability that contaminants will undergo reductive stabilization, however, is the chemical and physical heterogeneity of the media. Our research first examined microbially induced transformation of iron (hydr)oxide minerals and their impact on contaminant attenuation. We revealed that in intricate cascade of geochemical reactions is induced by microbially produced Fe(II), and that during transformation contaminants such as U(VI) can be incorporated into the structure, and a set of Fe(II) bearing solids capable of reducing Cr(VI) and stabilizing resulting Cr(III). We also note, however, that common subsurface constituents such as phosphate can modify iron oxide transformation pathways and thus impact contaminant sequestration - 'affecting both Cr and U

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

    International Nuclear Information System (INIS)

    Fendorf, Scott; Francis, Chris; Jardine, Phil; Benner, Shawn

    2009-01-01

    In situ stabilization (inclusive of natural attenuation) of toxic metals and radionuclides is an attractive approach for remediating many contaminated DOE sites. By immobilizing toxic metals and radionuclides in place, the removal of contaminated water to the surface for treatment as well as the associated disposal costs are avoided. To enhance in situ remediaton, microbiological reductive stabilization of contaminant metals has been, and continues to be, actively explored. It is likely that surface and subsurface microbial activity can alter the redox state of toxic metals and radionuclides, either directly or indirectly, so they are rendered immobile. Furthermore, anaerobic bacterial metabolic products will help to buffer pulses of oxidation, typically from fluxes of nitrate or molecular oxygen, and thus may stabilize reduced contaminants from oxidative mobilization. Uranium and chromium are two elements of particular concern within the DOE complex that, owing to their abundance and toxicity, appear well suited for biologically mediated reductive stabilization. Subsurface microbial activity can alter the redox state of toxic metals and radionuclides, rending them immobile. Imparting an important criterion on the probability that contaminants will undergo reductive stabilization, however, is the chemical and physical heterogeneity of the media. Our research first examined microbially induced transformation of iron (hydr)oxide minerals and their impact on contaminant attenuation. We revealed that in intricate cascade of geochemical reactions is induced by microbially produced Fe(II), and that during transformation contaminants such as U(VI) can be incorporated into the structure, and a set of Fe(II) bearing solids capable of reducing Cr(VI) and stabilizing resulting Cr(III). We also note, however, that common subsurface constituents such as phosphate can modify iron oxide transformation pathways and thus impact contaminant sequestration - affecting both Cr and U

  2. A new sub-equation method applied to obtain exact travelling wave solutions of some complex nonlinear equations

    International Nuclear Information System (INIS)

    Zhang Huiqun

    2009-01-01

    By using a new coupled Riccati equations, a direct algebraic method, which was applied to obtain exact travelling wave solutions of some complex nonlinear equations, is improved. And the exact travelling wave solutions of the complex KdV equation, Boussinesq equation and Klein-Gordon equation are investigated using the improved method. The method presented in this paper can also be applied to construct exact travelling wave solutions for other nonlinear complex equations.

  3. The application of iterative transformation factor analysis to resolve multi-component EXAFS spectra of uranium(6) complexes with acetic acid as a function of pH

    International Nuclear Information System (INIS)

    Robberg, A.; Reich, T.

    2002-01-01

    Synchrotron-based EXAFS spectroscopy is a powerful technique to obtain structural information on radionuclide complexes in solution. Depending on the chemical conditions of the samples several radionuclide species can coexist in the solution as is often the case for environmentally related samples. All radionuclide species, which may have different near-neighbour environments, contribute to the measured EXAFS signal. In order to isolate the EXAFS spectra of the individual species (pure spectral components), it is necessary, in a first step, to measure a series of samples where their composition is changed by variation of one physico-chemical parameter (e.g. pH, concentration, etc.). For the spectral decomposition it is necessary that the EXAFS signal change as a function of the chosen physico-chemical parameter. In a second step, the series of EXAFS spectra is analysed with Eigen analysis and Iterative Transformation Factor Analysis (ITFA). As a result of the ITFA one obtains: a) for each sample the relative concentration of the structural distinguishable species and b) their corresponding pure spectral components. From the information obtained in a), one can construct a speciation diagram. The pure spectral components contain the structural information of the individual species, which can be extracted by conventional EXAFS analysis. To evaluate our ITFA algorithm for EXAFS analysis of mixtures, we prepared a series of eight solution samples of 0.05 M uranium(VI) and 1 M acetate (Ac) in the pH range of 0.1 to 4.5. From thermodynamic constants it is known that under these conditions up to four species can occur: uranyl hydrate, and the 1:1, 1:2 and 1:3 complexes of uranyl acetate. The uranium L III -edge EXAFS spectra were measured at room temperature in transmission mode at the Rossendorf Beamline (ROBL) at the ESRF. The average bond length between uranium and the equatorial oxygen atoms (O eq ) increases from 2.40 to 2.46 angstrom with increasing pH. This increase

  4. Comparison between two sampling methods by results obtained using petrographic techniques, specially developed for minerals of the Itataia uranium phosphate deposit, Ceara, Brazil

    International Nuclear Information System (INIS)

    Salas, H.T.; Murta, R.L.L.

    1985-01-01

    The results of comparison of two sampling methods applied to a gallery of the uranium-phosphate ore body of Itataia-Ceara State, Brazil, along 235 metres of mineralized zone, are presented. The results were obtained through petrographic techniques especially developed and applied to both samplings. In the first one it was studied hand samples from a systematically sampling made at intervals of 2 metres. After that, the estimated mineralogical composition studies were carried out. Some petrogenetic observations were for the first time verified. The second sampling was made at intervals of 20 metres and 570 tons of ore extracted and distributed in sections and a sample representing each section was studied after crushing at -65. Their mineralogy were quantified and the degree of liberation of apatite calculated. Based on the mineralogical data obtained it was possible to represent both samplings and to make the comparison of the main mineralogical groups (phosphates, carbonates and silicates). In spite of utilizing different methods and methodology and the kind of mineralization, stockwork, being quite irregular, the results were satisfactory. (Author) [pt

  5. Study of new complexes of uranium and comba radical. II-Complexes formed in the presence of OH{sup -}, CO{sub 3}H{sup -}, CH{sub 3}-COO{sup -}, and B{sub 4}={sub 7}; Estudio de nuevos complejos entre uranio y el radical CADMBA. II. Complejos formados en presencia de OH{sup -}, CO{sub 3}H, CH{sub 3}-COO{sup -} y B{sub 4}O{sub 7}

    Energy Technology Data Exchange (ETDEWEB)

    Vera Palomino, V; Galiano Sedano, J A; Parellada Bellod, R; Bellido Gonzalez, A

    1975-07-01

    Several complexes extracted with CDMBAC organic solutions from uranium aqueous solutions, in presence of sodium and ammonium hydroxides, are studied. These complexes fit to the general formula: U0{sub 2}(OH){sub n}(CDMBA){sub n}-2 . The uranium extraction in presence of an excess of sodium bicarbonate is also studied. From aqueous solutions of uranyl acetate we have isolated the complex U0{sub 2}(CH{sub 3}-C00){sub n} (CDMBA){sub n}-2. In presence of boric acid and sodium tetraborate an U-CDMBA compound containing boron in its molecule has being obtained by precipitation and liquid-liquid extraction. (Author) 5 refs.

  6. A novel cetyltrimethyl ammonium silver bromide complex and silver bromide nanoparticles obtained by the surfactant counterion.

    Science.gov (United States)

    Liu, Xian-Hao; Luo, Xiao-Hong; Lu, Shu-Xia; Zhang, Jing-Chang; Cao, Wei-Liang

    2007-03-01

    A novel cetyltrimethyl ammonium silver bromide (CTASB) complex has been prepared simply through the reaction of silver nitrate with cetyltrimethyl ammonium bromide (CTAB) in aqueous solution at room temperature by controlling the concentration of CTAB and the molar ratio of CTAB to silver nitrate in the reaction solution, in which halogen in CTAB is used as surfactant counterion. The structure and thermal behavior of cetyltrimethyl ammonium silver bromide have been investigated by using X-ray diffraction (XRD), infrared spectroscopy (IR), X-ray photoelectron spectroscopy (XPS), UV/vis spectroscopy, thermal analysis (TG-DTA), transmission electron microscopy (TEM), and scanning electron microscopy (SEM). The results show that the complex possesses a metastable layered structure. Upon heating the CTASB aqueous dispersion to above 80 degrees C, the structure change of the complex took place and CTAB-capped nanosized silver bromide particles further formed.

  7. Immobilization of Mo(IV) complex in hybrid matrix obtained via sol-gel technique

    Energy Technology Data Exchange (ETDEWEB)

    Marques, C.; Sousa, A.M.; Freire, C.; Neves, I.C.; Fonseca, A.M.; Silva, C.J.R

    2003-10-06

    A molybdenum(IV) complex, trans-bis-[1,2-bis(diphenylphosphino)ethane]-fluoro-(diazopropano) -molybdenum tetraphenylborate, [MoF(DIAZO)(dppe){sub 2}][BPh{sub 4}], was prepared and immobilized in a hybrid matrix synthesized by the sol-gel process. The host matrix, designated as U(500), is an organic-inorganic network material, classed as ureasil, that combines a reticulated siliceous backbone linked by short polyether-based segments. Urea bridges make the link between these two components, and the polymerization of silicate substituted terminal groups generates the inorganic network. The free Mo(IV) complex and all new materials were characterized by spectroscopic techniques (FT-IR and UV-Vis) and thermal analysis (DSC). The ionic conductivity of the resulting material was also studied. The results indicate that immobilized Mo(IV) complex has kept its solid-state structure, although there is evidence of inter-molecular interactions between the Mo(IV) complex and some groups/atoms of the hybrid host matrix.

  8. Uranium management activities

    International Nuclear Information System (INIS)

    Jackson, D.; Marshall, E.; Sideris, T.; Vasa-Sideris, S.

    2001-01-01

    One of the missions of the Department of Energy's (DOE) Oak Ridge Office (ORO) has been the management of the Department's uranium materials. This mission has been accomplished through successful integration of ORO's uranium activities with the rest of the DOE complex. Beginning in the 1980's, several of the facilities in that complex have been shut down and are in the decommissioning process. With the end of the Cold War, the shutdown of many other facilities is planned. As a result, inventories of uranium need to be removed from the Department facilities. These inventories include highly enriched uranium (HEU), low enriched uranium (LEU), normal uranium (NU), and depleted uranium (DU). The uranium materials exist in different chemical forms, including metals, oxides, solutions, and gases. Much of the uranium in these inventories is not needed to support national priorities and programs. (author)

  9. Treatment of the X and γ rays lung monitoring spectra obtained by using HP-Ge detectors in case of exposures to uranium

    International Nuclear Information System (INIS)

    Berard, P.; Pourret, O.; Aussel, J.P.; Rongier, E.

    1996-01-01

    A lung monitoring counting spectrum can be described as a random phenomenon. Channel-by-channel Poisson-type modelling was verified for cases of pure background. When carrying out spectral analysis for qualitative research, one must work with the sum of the detectors. The quantification must be calculated detector by detector. Statistical tests make it possible to certify that one or several peaks are really present in the organism. The calculations are currently made with automatic spectral analysis, peak search, specific area, statistics and probability of the real presence of analytic photo peak taking into account the morphological parameters of the worker. The results are analysed detector by detector, with and without the background of the room. Detection limits obtained in Pierrelatte in monitoring measurement conditions were assessed for variable tissues covering the range of subjects to be examined. For each subject, the calculations are made taking into account the equivalent tissue thicknesses derived from individual morphological parameters. This method makes it possible to quantify lung activities with a detection limit of 3.9 Bq ( 235 U; thirty minutes counting time; reference man parameters) and to monitor exposure to the different compounds of uranium. (author)

  10. Project development for mining-metallurgical complexes for production of uranium concentrates - an analysis and a methodology

    International Nuclear Information System (INIS)

    Ajuria G, S.; Blanco P, B.; Pena A, J.; Manzanera Q, C.

    1978-10-01

    Activities comprising the development of a project for a mining-metallurgical complex for production of uranium concentrates, from sampling and evaluation of an orebody until plant start-up, are analyzed. The analysis of the orebody, characterization of the ore, bench scale and pilot plant metallurgical studies, environmental studies and economic analyses of the project are described. The mining project and mine preparation and engineering and construction of the plant are reviewed in less detail. The estimated time lapse for the development of a typical project under ideal conditions is 66 months. A bar diagram is included showing an approximate timetable for each activity. (author)

  11. Effect of denaturants on the speciation of uranium(VI) complexes of malonic acid in micellar media

    International Nuclear Information System (INIS)

    Sailaja, B.B.V.; Kebede, Tesfahun; Nageswara Rao, G.; Prasada Rao, M.S.

    2001-01-01

    A computer assisted investigation has been made on the nature of complexes of uranium(VI) with malonic acid. The formation constants have been determined experimentally by monitoring hydrogen ion concentration. The distribution of the metal ion amongst the complexes formed with the above carboxylic acid has also been computed. The formation constants have been refined with the computer program, MINIQUAD75 using the primary alkalimetric data. The predominant complexes formed are UO 2 (H 2 C 3 O 4 ) 2 ) 2- , UO 2 (H 2 C 3 O 4 ) and UO 2 (H 2 C 3 O 4 )(H 2 C 3 O 4 H) - . The distribution pattern of different species varies with the relative concentrations of the metal ion and the ligand. The variation of stability with surfactant concentrations is found to be the cumulative effect of various factors like electrostatic interactions. dilution effect and competition for hydrogen ion associated with the nature of micelles. (author)

  12. Synthesis and characterization of a uranium(III) complex containing a redox-active 2,2'-bipyridine ligand.

    Science.gov (United States)

    Kraft, Steven J; Fanwick, Phillip E; Bart, Suzanne C

    2010-02-01

    Hydrotris(3,5-dimethylpyrazolyl)borate uranium(III) diiodide derivatives have been prepared as an entry into low-valent uranium chemistry with these ligands. The bis(tetrahydrofuran) adduct, Tp*UI(2)(THF)(2) (1) (Tp* = hydrotris(3,5-dimethylpyrazolyl)borate), was synthesized by addition of sodium hydrotris(3,5-dimethylpyrazolyl)borate (NaTp*) to an equivalent of UI(3)(THF)(4). Addition of 2,2'-bipyridine (2,2'-bpy) to 1 displaced the THF molecules producing Tp*UI(2)(2,2'-bpy) (2). Both derivatives were characterized by (1)H NMR and IR spectroscopies, magnetic measurements, and X-ray crystallography. Reduction of both species was attempted with two equivalents of potassium graphite. The reduction of 1 did not result in a clean product, but rather decomposition and ligand redistribution. However, compound 2 was reduced to form Tp*(2)U(2,2'-bpy), 3, which is composed of a uranium(III) ion with a radical monoanionic bipyridine ligand. This was confirmed by X-ray crystallography, which revealed distortions in the bond lengths of the bipyridine consistent with reduction. Further support was obtained by (1)H NMR spectroscopy, which showed resonances shifted far upfield, consistent with radical character on the 2,2'-bipyridine ligand. Future studies will explore the reactivity of this compound as well as the consequences for redox-activity in the bipyridine ligand.

  13. Synthesis, structure, spectroscopy and redox energetics of a series of uranium(4) mixed-ligand metallocene complexes

    Energy Technology Data Exchange (ETDEWEB)

    Thomson, R.K.; Scott, B.L.; Morris, D.E.; Kiplinger, J.L. [Los Alamos National Laboratory, Los Alamos, NM (United States)

    2010-06-15

    A series of uranium(IV) mixed-ligand amide-halide/pseudo-halide complexes (C{sub 5}Me{sub 5}){sub 2}U[N(SiMe{sub 3}){sub 2}](X) (X = F (1), Cl (2), Br (3), I (4), N{sub 3} (5), NCO (6)), (C{sub 5}Me{sub 5}){sub 2}U(NPh{sub 2})(X) (X = Cl (7), N{sub 3} (8)), and (C{sub 5}Me{sub 5}){sub 2}U[N(Ph)(SiMe{sub 3})](X) (X Cl (9), N{sub 3} (10)) have been prepared by one electron oxidation of the corresponding uranium(III) amide precursors using either copper halides, silver iso-cyanate, or triphenylphosphine gold(I)azide. Agostic U---H-C interactions and {eta}{sub 3}-(N,C,C') coordination are observed for these complexes in both the solid-state and solution. There is a linear correlation between the chemical shift values of the C{sub 5}Me{sub 5} ligand protons in the {sup 1}H NMR spectra and the U(IV)/U(III) reduction potentials of the (C{sub 5}Me{sub 5}){sub 2}U[N(SiMe{sub 3}){sub 2}](X) complexes, suggesting that there is a common origin, that is overall {sigma}-/{pi}-donation from the ancillary (X) ligand to the metal, contributing to both observables. Optical spectroscopy of the series of complexes 1-6 is dominated by the (C{sub 5}Me{sub 5}){sub 2}U[N(SiMe{sub 3}){sub 2}] core, with small variations derived from the identity of the halide/pseudo-halide. The considerable {pi}-donating ability of the fluoride ligand is reflected in both the electrochemistry and UV-visible-NIR spectroscopic behavior of the fluoride complex (C{sub 5}Me{sub 5}){sub 2}U[N(SiMe{sub 3}){sub 2}](F) (1). The syntheses of the new trivalent uranium amide complex, (C{sub 5}Me{sub 5}){sub 2}U[N(Ph)(SiMe{sub 3})](THF), and the two new weakly-coordinating electrolytes, [Pr{sub 4}N][B{l_brace}3,5-(CF{sub 3}){sub 2}C{sub 6}H{sub 3{r_brace}4}] and [Pr{sub 4}N][B(C{sub 6}F{sub 5}){sub 4}], are also reported. (authors)

  14. Study of uranium +4 stabilization by the formation of a complex with a heteropolyanion ligand, for its off-lines analysis

    International Nuclear Information System (INIS)

    Bion, L.

    1995-01-01

    The study of the behaviour of uranium in oxidation state +4, during uranium/plutonium separation step of the PUREX process for reprocessing nuclear fuels, requires the availability of an efficient analytical method allowing the stabilization and off-line analysis of sample of aqueous and organic solutions containing this reagent. It was accordingly decided to develop a stabilization method using the heteropolyanion P 2 W 17 O 61 10- (PWO ' ) as a selective ligand. Besides the stabilization effect, the complexation of uranium +4 results in the appearance of an intense and specific band on the visible absorption spectrum of the formed U(PWO) 2 16- complex. This property made it possible to consider the sensitive spectrophotometric analysis of the sample. The work presented first helped to determine, in the presence of PWO, the characteristic thermodynamic data of the reaction involving uranium +4 and +6, plutonium +3 and +4, nitrous and nitric acids, and hydrazine. In the light of these results, it was possible to plan the development of the stabilisation method. The use of PWO thus helped (1) to design a method capable of stopping any reaction involving the uranium +4 / uranium +6 pair, and (2) to perform the simple analysis of uranium +4. The study presented in the second part uses the example of the U 4+ cation to understand the reasons for the selectivity of the complexation of actinides +4 by PWO. Owing to the remarkable spectroscopic and magnetic properties of this cation, ti was possible to acquire data concerning the structure of the U(PWO) 2 16- complex, both in solution and in the solid state. It was thus demonstrated that the geometry of the environment of U 4+ (eight oxygen forming a cubic anti-prism), which is perfectly complementary to that of the 5f electron wave functions of the actinide, helps to explain the selectivity of the complexation of actinides +4. (author). refs., 46 figs., 40 tabs

  15. The structure study of boron carbonitride films obtained by use of trimethylamine borane complex

    CERN Document Server

    Kosinova, M L; Fainer, N I; Maximovski, E A; Kuznetsov, F A

    2001-01-01

    Diffraction of synchrotron radiation (SR) was used to investigate crystalline structure and phase composition of thin films (1500-5000 A) of boron carbonitride. These films were synthesized by plasma-enhanced chemical vapor deposition using nontraditional volatile single source precursor trimethylamine borane complex (CH sub 3) sub 3 N centre dot BH sub 3 and its mixture with ammonia. The effect of the gas ratio and substrate temperature on chemical and phase composition as well as the structure of the films were investigated. The XRD peculiarities of texture films and ways of increasing sensibility of measurements were considered. A possibility of the information density rise of the thin film XRD was shown due to application of different methods for recording diffraction patterns.

  16. New complex fertilizer 'Suprodit' to obtain safe agricultural productions on contaminated lands.

    Science.gov (United States)

    Nikolaevich Ratnikov, Alexander; Sergeevich Anisimov, Vyacheslav; Nikoaevna Anisimova, Lidiya; Georgievich Sviridenko, Dmitry; Jurievna Balanova, Olesya

    2015-04-01

    One of the reclamation techniques to reduce the accumulation of radionuclides and heavy metals in the crop is the use of natural sorbents, industrial deposits of which are located in the contaminated areas or at distances that allows one to organize cheap their delivery to the application site. More promising reclamation technique is the use of new types of complex fertilizers, the main components of which are special sorbents of natural or artificial origin. New complex fertilizer of prolonged action - "SUPRODIT", containing in addition to nutrients highly efficient mineral and organic sorbents, was developed by specialists of the RIRAE. The feedstock for mineral sorbent was Tripoli (finely porous siliceous mineral) from local field (Kaluga region), organic sorbent - peat. The "SUPRODIT"composition: N - 8-11%; P2O5 - 11-13 %; K2O - 11-17%, organic matter and 30-40%, respectively. The effect of a single application of complex fertilizer will be maintained for two or more growing seasons. Received RF patent for the invention "Method of production of complex fertilizer of prolonged action". In a series of field experiments on sod-podzolic sandy loam soil it was shown that the application of "SUPRODIT" at dose of 800 kg/ha to soil contaminated with dehydrated sewage sludge (DSS), significantly reduces heavy metals (Cd, Ni, Pb) content in a crop of oats and barley due to the sorption properties of this fertilizers. Thus, Cd accumulation in the oats grain decreased 1.3 times, barley grain - 1.5 times, Ni - 1.5 times for barley and oats; Pb - 1.8 and 1.7 times respectively opposite to variant where the DSS was applied only. "SUPRODIT" reduces the negative effects of HM on the growth and development of plants, and limits the accumulation of 137Cs and HM in biomass. The 137Cs content in the biomass of barley in the variant of jointly added to soil of 137Cs and "SUPRODIT" decreased by 8.9 times in comparison with control and 4.4 times compared with standard fertilizers (NPK

  17. The effect of surfactants and complexing agents on the fluorimetric determination of uranium

    International Nuclear Information System (INIS)

    Pakalns, P.; Lane, H.T.

    1979-01-01

    The effect of surfactants, condensed phosphates, soap, EDTA, NTA, citric acid, oil and Alamine-336 on the fluorimetric determination of uranium in a 5-ml aqueous sample extracted with methyl isobutyl ketone after addition of saturated calcium nitrate or 1 N acid-deficient saturated aluminium nitrate salting-out solutions has been established. The error produced by these compounds, even at concentrations up to 500 mg/l, does not exceed = 10%, except for anionic LAS-type detergent, which at above the 50 mg/1 level forms stable emulsions after extraction from solutions containing the acid-deficient aluminium nitrate salting-out reagent. Up to 1 hour of standing time after extraction may be required for the emulsions to break. The detection limit for uranium is 1.1 μg (2s). (author)

  18. Cyclopentadienyl complexes of uranium(IV) chlorides. Crystal structures of trichloro(eta5-cyclopentadienyl)bis(triphenylphosphine oxide)uranium(IV) tetrahydrofuran solvate and of trichloro(eta5-cyclopentadienyl)bis(hexamethylphosphoramide)uranium(IV)

    International Nuclear Information System (INIS)

    Bagnall, K.W.; De Paoli, G.

    1984-01-01

    The crystal and molecular structures of [U(cp)Cl 3 (PPh 3 O) 2 ].thf (thf = tetrahydrofuran) (1) and [U(cp)Cl 3 (P(NMe 2 ) 3 O) 2 ] (cp = eta 5 -cyclopentadienyl) (2) have been determined from three-dimensional X-ray diffraction data. The results are presented. In both compounds the uranium atom is octahedrally co-ordinated with the two neutral ligands [PPh 3 O and P(NMe 2 ) 3 O] in cis positions; the chlorine atoms are in the mer arrangement and the cyclopentadienyl group is trans to one neutral ligand. The appearance of cis octahedral geometry in complexes of the type [U(cp)Cl 3 L 2 ] is discussed in terms of the operation of a possible trans effect. (author)

  19. Extraction of bivalent vanadium as its pyridine thiocyanate complex and separation from uranium, titanium, chromium and aluminium

    International Nuclear Information System (INIS)

    Yatirajam, V.; Arya, S.P.

    1975-01-01

    A simple method is described for the extraction of V(II) as its pyridine thiocyanate complex. Vanadate is reduced to V(II) in 1 to 2 N sulphuric acid by zinc amalgam. Thiocyanate and pyridine are added, the solution is adjusted to pH 5.2 to 5.5 and the complex extracted with chloroform. The vanadium is back-extracted with peroxide solution. Zinc from the reductant accompanies the vanadium but alkali and alkaline earth metal ions, titanium, uranium, chromium and aluminium are separated, besides those ions reduced to the elements by zinc amalgam. The method takes about 20 min and is applicable to microgram as well as milligram amounts of vanadium. (author)

  20. Uranium sorption to natural substrates-insights provided by isotope exchange, selective extraction and surface complexation modelling approaches

    International Nuclear Information System (INIS)

    Waite, T.D.; Payne T.E.; Davis, J.A.

    1993-01-01

    An extensive experimental program has been conducted over the last three years into the interaction of U(VI) with both single oxides and clays and complex natural substrates from the weathered zone in the vicinity of a uranium ore body in northern Australia. While iron oxides have frequently been considered to account for much of the uptake on such natural substrates, the results of laboratory open-quotes pH edgeclose quotes studies and of isotope exchange and selective extraction studies suggest that other phases must also play a significant role in controlling the partitioning of U(VI) between solid and solution phases. Supporting studies on kaolinite, the dominant clay in this system, provide insight into the most appropriate method of modelling the interaction of U(VI) with these natural substrates. The problems still remaining in adequately describing sorption of radionuclides and trace elements to complex natural substrates are discussed

  1. Uranium leaching analysis (IAEA method) and total uranium determination in caldasite by the fluorometric method

    International Nuclear Information System (INIS)

    Sardela, I.A.; Fujimori, K.

    1980-10-01

    Caldasite is a radioactive mineral known mostly for its high radioactive content (U and Th). It is found only at the Pocos de Caldas Alkaline Complex, States of Minas Gerais. Samples colected at Campos do Serrote, Taquari and Brigrada located in the alkaline complex were submitted to the fluorometric method of uranium analysis. The results show a good precision and close agreement with those obtained with gamma ray spectroscopy. IAEA uranium leaching analysis has also been applied to this mineral, but only 0,4% of the total content was dissolved. The uranium leaching was more intense on the samples that have smaller equivalent uranium than total uranium and it may be attributed to a higher range Rn gas escape from this mineral. (Author) [pt

  2. Sponge-like silver obtained by decomposition of silver nitrate hexamethylenetetramine complex

    International Nuclear Information System (INIS)

    Afanasiev, Pavel

    2016-01-01

    Silver nitrate hexamethylenetetramine [Ag(NO 3 )·N 4 (CH 2 ) 6 ] coordination compound has been prepared via aqueous route and characterized by chemical analysis, XRD and electron microscopy. Decomposition of [Ag(NO 3 )·N 4 (CH 2 ) 6 ] under hydrogen and under inert has been studied by thermal analysis and mass spectrometry. Thermal decomposition of [Ag(NO 3 )·N 4 (CH 2 ) 6 ] proceeds in the range 200–250 °C as a self-propagating rapid redox process accompanied with the release of multiple gases. The decomposition leads to formation of sponge-like silver having hierarchical open pore system with pore size spanning from 10 µm to 10 nm. The as-obtained silver sponges exhibited favorable activity toward H 2 O 2 electrochemical reduction, making them potentially interesting as non-enzyme hydrogen peroxide sensors. - Graphical abstract: Thermal decomposition of silver nitrate hexamethylenetetramine coordination compound [Ag(NO 3 )·N 4 (CH 2 ) 6 ] leads to sponge like silver that possesses open porous structure and demonstrates interesting properties as an electrochemical hydrogen peroxide sensor. Display Omitted - Highlights: • [Ag(NO 3 )·N 4 (CH 2 ) 6 ] orthorhombic phase prepared and characterized. • Decomposition of [Ag(NO 3 )·N 4 (CH 2 ) 6 ] leads to metallic silver sponge with opened porosity. • Ag sponge showed promising properties as a material for hydrogen peroxide sensors.

  3. Solvothermal synthesis of uranium(VI) phases with aromatic carboxylate ligands: A dinuclear complex with 4-hydroxybenzoic acid and a 3D framework with terephthalic acid

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Yingjie, E-mail: yzx@ansto.gov.au [Australian Nuclear Science and Technology Organisation, Locked Bag 2001, Kirrawee DC, NSW 2232 (Australia); Karatchevtseva, Inna [Australian Nuclear Science and Technology Organisation, Locked Bag 2001, Kirrawee DC, NSW 2232 (Australia); Bhadbhade, Mohan [Mark Wainwright Analytical Centre, University of New South Wales, Kensington, NSW 2052 (Australia); Tran, Toan Trong; Aharonovich, Igor [School of Physics and Advanced Materials, University of Technology Sydney, Ultimo, NSW 2007 (Australia); Fanna, Daniel J.; Shepherd, Nicholas D. [School of Science and Health, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751 (Australia); Lu, Kim [Australian Nuclear Science and Technology Organisation, Locked Bag 2001, Kirrawee DC, NSW 2232 (Australia); Li, Feng [School of Science and Health, Western Sydney University, Locked Bag 1797, Penrith, NSW 2751 (Australia); Lumpkin, Gregory R. [Australian Nuclear Science and Technology Organisation, Locked Bag 2001, Kirrawee DC, NSW 2232 (Australia)

    2016-02-15

    With the coordination of dimethylformamide (DMF), two new uranium(VI) complexes with either 4-hydroxybenzoic acid (H{sub 2}phb) or terephthalic acid (H{sub 2}tph) have been synthesized under solvothermal conditions and structurally characterized. [(UO{sub 2}){sub 2}(Hphb){sub 2}(phb)(DMF)(H{sub 2}O){sub 3}]·4H{sub 2}O (1) has a dinuclear structure constructed with both pentagonal and hexagonal bipyramidal uranium polyhedra linked through a µ{sub 2}-bridging ligand via both chelating carboxylate arm and alcohol oxygen bonding, first observation of such a coordination mode of 4-hydroxybenzoate for 5 f ions. [(UO{sub 2})(tph)(DMF)] (2) has a three-dimensional (3D) framework built with pentagonal bipyramidal uranium polyhedra linked with µ{sub 4}-terephthalate ligands. The 3D channeled structure is facilitated by the unique carboxylate bonding with nearly linear C–O–U angles and the coordination of DMF molecules. The presence of phb ligands in different coordination modes, uranyl ions in diverse environments and DMF in complex 1, and tph ligand, DMF and uranyl ion in complex 2 has been confirmed by Raman spectroscopy. In addition, their thermal stability and photoluminescence properties have been investigated. - Graphical abstract: With the coordination of dimethylformamide, two new uranyl complexes with either 4-hydroxybenzoate or terephthalate have been synthesized under solvothermal conditions and structurally characterized. - Highlights: • Solvent facilitates the synthesis of two new uranium(VI) complexes. • A dinuclear complex with both penta- and hexagonal bipyramidal uranium polyhedral. • A unique µ{sub 2}-bridging mode of 4-hydroxybenzoate via alcohol oxygen for 5 f ions. • A 3D framework with uranium polyhedra and µ{sub 4}-terephthalate ligands. • Vibration modes and photoluminescence properties are reported.

  4. Sponge-like silver obtained by decomposition of silver nitrate hexamethylenetetramine complex

    Energy Technology Data Exchange (ETDEWEB)

    Afanasiev, Pavel, E-mail: pavel.afanasiev@ircelyon.univ-lyon.fr

    2016-07-15

    Silver nitrate hexamethylenetetramine [Ag(NO{sub 3})·N{sub 4}(CH{sub 2}){sub 6}] coordination compound has been prepared via aqueous route and characterized by chemical analysis, XRD and electron microscopy. Decomposition of [Ag(NO{sub 3})·N{sub 4}(CH{sub 2}){sub 6}] under hydrogen and under inert has been studied by thermal analysis and mass spectrometry. Thermal decomposition of [Ag(NO{sub 3})·N{sub 4}(CH{sub 2}){sub 6}] proceeds in the range 200–250 °C as a self-propagating rapid redox process accompanied with the release of multiple gases. The decomposition leads to formation of sponge-like silver having hierarchical open pore system with pore size spanning from 10 µm to 10 nm. The as-obtained silver sponges exhibited favorable activity toward H{sub 2}O{sub 2} electrochemical reduction, making them potentially interesting as non-enzyme hydrogen peroxide sensors. - Graphical abstract: Thermal decomposition of silver nitrate hexamethylenetetramine coordination compound [Ag(NO{sub 3})·N{sub 4}(CH{sub 2}){sub 6}] leads to sponge like silver that possesses open porous structure and demonstrates interesting properties as an electrochemical hydrogen peroxide sensor. Display Omitted - Highlights: • [Ag(NO{sub 3})·N{sub 4}(CH{sub 2}){sub 6}] orthorhombic phase prepared and characterized. • Decomposition of [Ag(NO{sub 3})·N{sub 4}(CH{sub 2}){sub 6}] leads to metallic silver sponge with opened porosity. • Ag sponge showed promising properties as a material for hydrogen peroxide sensors.

  5. New french uranium mineral species

    International Nuclear Information System (INIS)

    Branche, G.; Chervet, J.; Guillemin, C.

    1952-01-01

    In this work, the authors study the french new uranium minerals: parsonsite and renardite, hydrated phosphates of lead and uranium; kasolite: silicate hydrated of uranium and lead uranopilite: sulphate of uranium hydrated; bayleyite: carbonate of uranium and of hydrated magnesium; β uranolite: silicate of uranium and of calcium hydrated. For all these minerals, the authors give the crystallographic, optic characters, and the quantitative chemical analyses. On the other hand, the following species, very rare in the french lodgings, didn't permit to do quantitative analyses. These are: the lanthinite: hydrated uranate oxide; the α uranotile: silicate of uranium and of calcium hydrated; the bassetite: uranium phosphate and of hydrated iron; the hosphuranylite: hydrated uranium phosphate; the becquerelite: hydrated uranium oxide; the curite: oxide of uranium and lead hydrated. Finally, the authors present at the end of this survey a primary mineral: the brannerite, complex of uranium titanate. (author) [fr

  6. Multisensor system for determination of iron(II), iron(III) and uranium(VI) in complex solutions

    International Nuclear Information System (INIS)

    Legin, A.V.; Seleznev, B.L.; Rudnitskaya, A.M.; Vlasov, Yu.G.

    1998-01-01

    The aim of the present paper is the development and analytical evaluation of a multisensor system for determination of low content of iron(II), iron(III) and uranium(VI) in complex aqueous media. Sensor array included sensors on the basis of chalcogenide vitreous materials with redox and ionic cross-sensitivities, crystalline silver sulphide electrode, noble metal electrodes Pt, Au, Ag and redox sensor on the basis of oxide glass. Potentiometric measurements have been taken in a conventional electrochemical cell vs. a standard Ag/AgCl reference electrode. All measurements have been taken at room temperature. Calibration solutions contained UO 2 (NO 3 ) 2 in concentration range 10 -6 -1,610 -5 mol/L, K 3 Fe(CN) 6 and K 4 Fe(CN) 6 or FeSO 4 (NH 4 ) 2 SO 4 and FeCl 3 , with the ratio of Fe(II)/Fe(III) concentration from 100:1 to 1:100, the total concentration of Fe was 10 -4 and 10 -5 mol/L. All solutions have been made on the background electrolyte of calcium and magnesium chlorides and sulphates with the fixed content of 5-27 mmol/L of each component which is a typical one for groundwater or mining water. Sensor potentials have been processed by a back-propagation artificial neural net. Average error of determination of Fe(II) and Fe(III) is about 20 %, of uranium(VI) - 40 %. It was found that sensitivity of the sensor array to iron and uranium is irrespective of the chemical form of these species

  7. Steric control of redox events in organo-uranium chemistry: synthesis and characterisation of U(V) oxo and nitrido complexes

    OpenAIRE

    Tsoureas, Nikolaos; Kilpatrick, Alexander; Inman, Christopher; Cloke, Frederick Geoffrey

    2016-01-01

    The synthesis and molecular structures of a U(V) neutral terminal oxo complex and a U(V) sodium uranium nitride contact ion pair are described. The synthesis of the former is achieved by the use of tBuNCO as a mild oxygen transfer reagent, whilst that of the latter is via the reduction of NaN3. Both mono-uranium complexes are stabilised by the presence of bulky silyl substituents on the ligand framework that facilitate a 2e- oxidation of a single U(III) centre. In contrast, when steric hindra...

  8. Crystal and molecular structures of thorium and uranium tetrakis(hexafluoroacetonylpyrazolide) complexes

    International Nuclear Information System (INIS)

    Volz, K.; Zalkin, A.; Templeton, D.H.

    1976-01-01

    Triclinic crystals of thorium(IV) and uranium(IV) tetrakis(hexafluoroacetonylpyrazolide) are isostructural, with space group P1 and Z = 2. At 23 0 C for Th(C 6 H 3 ON 2 F 6 ) 4 α = 11.282 (5) A, b = 16.245 (7) A, c = 10.836 (5) A, α = 90.14 (5) 0 , β = 108.75 (5) 0 , and γ = 107.07 (5) 0 . For the uranium compound a = 11.302 (5) A, b = 16.377 (8) A, c = 11.000 (5) A, α = 87.85 (5) 0 , β = 111.02 (5) 0 , and γ = 109.95 (5) 0 . X-ray diffraction data were measured with a scintillation counter, theta-2theta scans, and Mo Kα radiation. For thorium the conventional R value is 0.026 for 2966 unique data with I greater than sigma(I), and for uranium it is 0.027 for 4125 unique data with I greater than sigma(I). The full-matrix least-squares refinement of the 598 parameters of each structure included anisotropic thermal parameters for the 61 nonhydrogen atoms and isotropic ones for the 12 hydrogen atoms. The actinide ion is at the center of an irregular polyhedron of four oxygen and four nitrogen atoms. The average Th-O, Th-N, U-O, and U-N distances are 2.291 (4), 2.637 (5), 2.237 (3), and 2.574 (5) A. The molecules are packed in a manner which resembles cubic closest packing but which is more nearly analogous to the body-centered tetragonal structure of protactinium metal

  9. Installation of Radiometric Sorting throughout the Cogema-Simo Mining Complex at Lodeve. [Uranium ores

    Energy Technology Data Exchange (ETDEWEB)

    Grenier, J.; Winter, J.M.; Deville, P.

    1986-06-01

    The ores of Lodeve present no physical characteristics which permit an elimination of the lowest grade fractions, with the exception of the radioactivity and the radium which accompanies the uranium. The mine therefore turned to radiometric pebble-by-pebble sorting on a machine model M 17 of Ore Sorters who have a monopoly of this type of equipment; this permits an operation over a size range from 25 to 160 mm. Sampling of the deposit investigation of pebble samples, construction of the sorting plant and commissioning are described.

  10. Study of new complexes of uranium and comba radical. I.- Complexes defective in sodium carbonate; Estudio de nuevos complejos entre el uranio y el radical CDMBA. I. Complejos con defectos de carbonato sodico

    Energy Technology Data Exchange (ETDEWEB)

    Vera Palomino, J; Galiano Sedano, J A; Parellada Bellod, R; Bellido Gonzalez, A

    1975-07-01

    Some complexes formed in presence of defect of sodium carbonate with respect to the stoichiometric ratio (U): (C0{sub 3}) = 1:3 are studied. This ratio corresponds to the main complex which is responsible for the uranium extraction with CDMBAC organic solutions and from U(VI) aqueous solutions with an excess of sodium carbonate. (Author) 10 refs.

  11. Complexation modeling of uranium and other actinides by organic compounds of natural or synthetic origin

    International Nuclear Information System (INIS)

    Bouby, M.

    1998-01-01

    The behaviour of nuclear wastes raises many questions, the answers of which require a precise knowledge of the physical, chemical and biological processes affecting the properties of the radio-elements present in the wastes. Three ways of research are approached. The results obtained give some elements of answer to these questions. The experimental methods that have been used are the neutron activation analysis, the UV-visible spectrophotometry, and the time-resolved laser spectro-fluorimetry. The analysis of the results has permitted to model part of the phenomena evidenced by using suitable ionic force correction models (Davies or MSA type) when chemical equilibria have been considered. The main results show: the bio-sorption capacities of Mycobacterium phlei microorganism with respect to UO 2 2+ and NpO 2+ cations such as: Q eq (UO 2 2+ ) = 60 and Q eq (NpO 2+ ) = 444 moles of cation per g of dry biomass; the retention capacities, in various leaching conditions, of this bacteria of the preliminarily adsorbed ions; the complexation properties of two siderophores with respect to UO 2 2+ , U 4+ and Th 4+ cations. One siderophore, Pyoverdine A, shows a selectiveness which is explained by the value of the thermodynamic equilibrium constant determined for each cation using the same model: K(UO 2 2+ ) 4+ ) 4+ ). The behaviour in highly acid environment (HCl and HClO 4 up to 12 M) of acylisoxazolone HPBI (1-phenyl-4-benzoyl-5-isoxazolone) and the value of its acidity thermodynamical constant (0.13 th 4 and CF 3 SO 3 H up to 12 M). It seems that a complexation between uranyl and the counter-ions present in the solution occurs. (J.S.)

  12. Obtaining isochrones from pollution signals in a fluvial sediment record: A case study in a uranium-polluted floodplain of the Ploučnice River, Czech Republic

    International Nuclear Information System (INIS)

    Matys Grygar, T.; Elznicová, J.; Bábek, O.; Hošek, M.; Engel, Z.; Kiss, T.

    2014-01-01

    Highlights: • Integrated approach to assess pollutant distribution in floodplain. • Natural background concentration is a function and not a value. • Concept of local enrichment factors based on local background functions. • Secondary pollution from transient fluvial deposits. - Abstract: Uranium mining and processing in the watershed of the Ploučnice River in the Czech Republic during a well-defined time interval (1969–1989) allowed for a study of pollutant fates in sediments of a meandering river that is otherwise in a nearly natural state. A considerable part of the primary pollution is present in hotspots in the floodplain 10–15 km downstream from the mining district. One of the hotspots was characterised using geoinformatic, geophysical and geochemical means. The floodplain geomorphology and architecture and river channel dynamics were studied to develop an understanding of the formation of the hotspot and evaluate further movement of pollutants in the river system. Local background functions (with Rb or Ti as a predictor) and local enrichment factors (LEFs) were obtained for Ba, Ni, Pb, U and Zn concentrations in unpolluted sediments from the deeper strata of the active floodplain, an abandoned floodplain and an ancient terrace. The most recent (2013) overbank fines in the study area are still considerably enriched in Ni, U and Zn (LEF 3, 6 and 8, respectively), and thus pollution by heavy metals several km downstream of the hotspots continuously increases even though the primary source of pollution was terminated more than 20 years ago. The onset of the primary pollution (the base of the polluted strata) is hence clearly identified in the distal floodplain sediments as persistent and a potentially isochronous pollution signal in the fluvial record, whereas a secondary pollution signal overwrites the expected “primary pollution climax” and “pollution improvement” signals. That inertia of the fluvial system can also be expected in other

  13. Uranium recovery from phosphonitric solutions

    International Nuclear Information System (INIS)

    Bunus, F.T.; Miu, I.

    1997-01-01

    A new technology for uranium and rare earth recovery applied in a semi-industrial plant processing 5 m 3 /h phosphoric acid has been extended to phosphonitric solution, resulting in the process of nitric acid attack of phosphate rock for complex fertilizer production. In this process uranium and rare earths are obtained at larger quantities due to the complete dissolution of elements involved. The method is based on a one cycle extraction-stripping process using as extractants: di(2-ethylhexyl) phosphate (DEPA) in mixture either with tri-n-butylphosphate (TBP) or tri-n-octylphosphine oxide (TOPO) in view of obtaining a synergic effect for U (VI). A mixer-settler extractor in four steps was used. Two stripping steps are involved for the elements mentioned. Before uranium stripping a scrubbing with urea was introduced to eliminate nitric acid extracted. Uranium was obtained as green cake (hydrated uranium tetrafluoride) which can be easily transformed in hexfluoride or converted to a diuranate. At the same time the radium is also eliminated leading to a non-radioactive fertilizer product. (author),. 8 refs, 4 figs

  14. Simultaneous precipitation of carbonato complexes of uranium and plutonium with cationic surfactants

    International Nuclear Information System (INIS)

    Heckmann, K.; Strnad, J.; Huber, K.

    1992-01-01

    The proposed method allows to separate Uranium, Thorium and Cerium from carbonate solutions and the further processing of these metals to mixed oxides. The separation can be divided into three steps: 1. Precipitation of the metals with a 10-fold surplus of carbonate and a 5-fold surplus of a cationic surfactant. 2. Thermal decomposition of the precipitates in air at 600 C. 3. Reduction of U(VI) to U(IV) with CO at 500 C. Mixed oxides in any ratio are formed in this way. This is possible due to the coprecipitation of both metals. Comparing the standard potentials it is clear that Ce(IV) is more easily reduced that Pu(IV). Therefore, the chance on the formation of U/Pu mixed oxides by this method is quite good. (orig.) [de

  15. Chemical shift of U L3 edges in different uranium compounds obtained by X-ray absorption spectroscopy with synchrotron radiation

    International Nuclear Information System (INIS)

    Joseph, D.; Jha, S.N.; Nayak, C.; Bhattacharyya, D.; Babu, P. Venu

    2014-01-01

    Uranium L 3 X-ray absorption edge was measured in various compounds containing uranium in U 4+ , U 5+ and U 5+ oxidation states. The measurements have been carried out at the Energy Dispersive EXAFS beamline (BL-08) at INDUS-2 synchrotron radiation source at RRCAT, Indore. Energy shifts of ∼ 2-3 eV were observed for U L 3 edge in the U-compounds compared to their value in elemental U. The different chemical shifts observed for the compounds having the same oxidation state of the cation but different anions or ligands show the effect of different chemical environments surrounding the cations in determining their X-ray absorption edges in the above compounds. The above chemical effect has been quantitatively described by determining the effective charges on U cation in the above compounds. (author)

  16. Influence of phosphates when uranium in solutions obtained by attacking Forez with sulfuric acid is precipitated by the action of lime; Influence des phosphates, lors de la precipitation par la chaux, de l'uranium contenu dans les solutions d'attaque sulfurique du Forez

    Energy Technology Data Exchange (ETDEWEB)

    Brebec, G

    1959-03-01

    Influence of phosphates when uranium in solutions obtained by attacking Forez with sulfuric acid is precipitated by the action of lime was studied. Most of the phosphates were eliminated in the form of ferric phosphates without noticeable losses of uranium: for this it is only necessary to add sufficient ferric sulfate to the solution to be treated so that [Po{sub 4}{sup 3-}]/[Fe{sup 3+}] {approx} 0,4. In these conditions, the preparation of a calcium concentrate rich in uranium takes place in two stages. The first is neutralization at pH 2,7 to 2,8 with elimination of phosphates, sulfates and iron; the second is precipitation of the concentrate at pH 6,5. (author) [French] Nous avons reussi a eliminer la majeure partie des phosphates sous forme de phosphates ferriques, sans pertes sensibles d'uranium. Pour cela, il suffit d'ajouter a la solution a traiter, du sulfate ferrique en quantite telle que: (Po{sub 4}{sup 3-}]/[Fe{sup 3+}] {approx} 0,4. Dans ces conditions, la preparation du concentre calcique, riche en uranium, s'effectue normalement en deux temps: 1) preneutralisation a pH 2,7-2,8: elimination des sulfates, phosphates et fer; 2) precipitation du concentre a pH 6,5. (auteur)

  17. Synthesis and characterization of chiral thorium(IV) and uranium(IV) benzamidinate complexes

    Energy Technology Data Exchange (ETDEWEB)

    Schoene, Sebastian; Maerz, Juliane; Kaden, Peter; Patzschke, Michael; Ikeda-Ohno, Atsushi [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Chemistry of the F-Elements

    2017-06-01

    Two chiral benzamidinate complexes of tetravalent actinides (Th(IV) and U(IV)) were synthesized using a salt metathesis reaction of the corresponding actinide(IV) tetrachlorides and the potassium salt of the chiral benzamidine (S,S)-N,N-Bis-(1-phenylethyl)-benzamidine ((S)-HPEBA). The structure of the complexes was determined with single crystal X-ray diffraction. These are the first examples of chiral amidinate complexes of actinides.

  18. Macrocyclic ligands for uranium complexation. Final report, August 1, 1986--March 31, 1993

    International Nuclear Information System (INIS)

    Potts, K.T.

    1993-01-01

    Macrocycles, designed for complexation of the uranyl ion by computer modeling studies and utilizing six ligating atoms in the equatorial plane of the uranyl ions, have been prepared and their complexation of the uranyl ions evaluated. The ligating atoms, either oxygen or sulfur, were part of acylurea, biuret or thiobiuret subunits with alkane chains or pyridine units completing the macrocyclic periphery. These macrocycles with only partial preorganization formed uranyl complexes in solution but no crystalline complexes were isolated. Refinement of the cavity diameter by variation of the peripheral functional groups is currently studied to achieve an optimized cavity diameter of 4.7--5.2 angstrom. Acyclic ligands containing the same ligating atoms in equivalent functional entities were found to form a crystalline 1:1 uranyl-ligand complex (stability constant log K = 10.7) whose structure was established by X-ray data. This complex underwent a facile, DMSO-induced rearrangement to a 2:1 uranyl-ligand complex whose structure was also established by X-ray data. The intermediates to the macrocycles all behaved as excellent ligands for the complexation of transition metals. Acylthiourea complexes of copper and nickel as well as intermolecular, binuclear copper and nickel complexes of bidentate carbonyl thioureas formed readily and their structures were established in several representative instances by X-ray structural determinations. Tetradentate bis(carbonylthioureas) were found to be very efficient selective reagents for the complexation of copper in the presence of nickel ions. Several preorganized macrocycles were also prepared but in most instances these macrocycles underwent ring-opening under complexation conditions

  19. Redox reactivity and coordination chemistry of uranium

    International Nuclear Information System (INIS)

    Nocton, G.

    2009-09-01

    The study and the understanding of actinides chemistry have important implications in the nuclear field both for the development of new actinides materials and the retreatment of the nuclear wastes. One of the major issues in that chemistry is that the actinides elements are known to undergo redox reaction and to form assemblies of different size and different topologies. In that context uranium can be a good model of the heavier radioelement because it is much less radioactive. So, this work concerns the synthesis and the study of the spectroscopy and the magnetic properties of several uranium based polymetallic assemblies synthesized by taking advantage of the redox properties and the coordination chemistry of uranium. The hydrolysis reactivity of trivalent uranium has been studied in absence of sterically hindered ligands and led to the synthesis of oxo/hydroxo uranium assemblies with different sizes by changing the starting complex or the reaction conditions. By following the same strategy, the controlled oxidation of trivalent uranium complexes led to an original azido/nitrido uranium complex. The coordination chemistry of the pentavalent uranyl polymer {[UO 2 py 5 ][KI 2 py 3 ]} n has also been studied with different ligand and in different conditions and led to several cation-cation complexes for which the stability is sufficient for studying there dismutation by proton NMR. By changing the ancillary ligands stable monomeric complexes of pentavalent uranyl complexes were also obtained. The magnetic properties of all the complexes, monomers and polymetallic complexes were studied and an antiferromagnetic coupling was observed for the cation-cation pentavalent uranyl dimer [UO 2 (dbm) 2 (K 18 C 6 )] 2 . (author)

  20. Macrocyclic ligands for uranium complexation: Progress report, August 15, 1987-present

    International Nuclear Information System (INIS)

    Potts, K.T.

    1988-03-01

    The synthesis of several macrocyclic ligands, designed by a computer modeling approach for the complexation of the uranyl ion, has now been completed and their structures established. Preliminary indicate that these macrocycles successfully complex the uranyl ion. Other synthetic efforts have led to a variety of intermediates suitable for final ring closure to the desired macrocycles, providing appreciable potential for variation of the macrocyclic peripheral atoms. A 1:1-uranyl ion complex of one of these precursor products has been shown to undergo a DMSO-induced rearrangement to a 2:1 uranyl ion to ligand complex, both structures having been established by single crystal x-ray data. 10 refs

  1. Mixed-ligand complexes of zirconium (IV) and uranium with salicylaldehyde and some heterocyclic azopyrazolones

    International Nuclear Information System (INIS)

    Amrallahi, A.H.

    1994-01-01

    Mixed-ligand complexes of Zr(IV) and U(IV) with salicylaldehyde (SA) and some heterocyclic azopyrazolenes have been studied spectrophotometrically. All formed chelates have ratio 1:1:1. The stoichiometry and stability of the binary mixed chelates been evaluated. Elemental analysis, molar conductance and IR spectra have been used for identification of solid mixed complexes. (author)

  2. Determination of uranium and thorium in complex matrices by two solvent extraction separation techniques and photon electron rejecting alpha liquid spectrometry

    International Nuclear Information System (INIS)

    Ayranov, M.; Wacker, L.; Kraehenbuehl, U.

    2001-01-01

    The separation of uranium and thorium from complex matrixes such as marine sediments using solvent extraction and determination by means of photon-electron rejecting liquid alpha spectrometry (PERALS trademark) has successfully been performed. Two extraction schemes, using TOPO and HDEHP, respectively, were compared for the separation of uranium and thorium from the matrix components. The results show recoveries between 73 and 92% for 234 U, 238 U, 232 Th, 230 Th and 238 Th with an accuracy of the methods ±12%. Minimum detectable activities for counting time up to 500 000 seconds for 0.5 g sample material were between 0.34-1.15 Bq/kg for uranium and 0.31-1.66 Bq/kg for thorium. (orig.)

  3. Uranium mining

    International Nuclear Information System (INIS)

    2008-01-01

    Full text: The economic and environmental sustainability of uranium mining has been analysed by Monash University researcher Dr Gavin Mudd in a paper that challenges the perception that uranium mining is an 'infinite quality source' that provides solutions to the world's demand for energy. Dr Mudd says information on the uranium industry touted by politicians and mining companies is not necessarily inaccurate, but it does not tell the whole story, being often just an average snapshot of the costs of uranium mining today without reflecting the escalating costs associated with the process in years to come. 'From a sustainability perspective, it is critical to evaluate accurately the true lifecycle costs of all forms of electricity production, especially with respect to greenhouse emissions, ' he says. 'For nuclear power, a significant proportion of greenhouse emissions are derived from the fuel supply, including uranium mining, milling, enrichment and fuel manufacture.' Dr Mudd found that financial and environmental costs escalate dramatically as the uranium ore is used. The deeper the mining process required to extract the ore, the higher the cost for mining companies, the greater the impact on the environment and the more resources needed to obtain the product. I t is clear that there is a strong sensitivity of energy and water consumption and greenhouse emissions to ore grade, and that ore grades are likely to continue to decline gradually in the medium to long term. These issues are critical to the current debate over nuclear power and greenhouse emissions, especially with respect to ascribing sustainability to such activities as uranium mining and milling. For example, mining at Roxby Downs is responsible for the emission of over one million tonnes of greenhouse gases per year and this could increase to four million tonnes if the mine is expanded.'

  4. Ternary uranium(VI) carbonato humate complex studied by cryo-TRLFS

    International Nuclear Information System (INIS)

    Steudtner, R.; Sachs, S.; Schmeide, K.; Brendler, V.; Bernhard, G.

    2011-01-01

    The complex formation of U(VI) with humic acid (HA) in the presence of carbonate was studied by time-resolved laser-induced fluorescence spectroscopy at low temperature (cryo-TRLFS) at pH 8.5. In the presence of HA, a decrease of the luminescence intensity of U(VI) and no shift of the emission band maxima in comparison to the luminescence spectrum of the UO 2 (CO 3 ) 3 4- complex, the dominating U(VI) species under the applied experimental conditions in the absence of HA, was observed. The formation of a ternary U(VI) carbonato humate complex of the type UO 2 (CO 3 ) 2 HA(II) 4- starting from UO 2 (CO 3 ) 3 4- was concluded from the luminescence data. For this complex a complex stability constant of log K=2.83 ± 0.17 was determined. Slope analysis resulted in a slope of 1.12 ± 0.11, which verifies the postulated complexation reaction. The results agree very well with literature data. Speciation calculations show that the formation of the ternary U(VI) carbonato humate complex can significantly influence the U(VI) speciation under environmental conditions. (orig.)

  5. Ternary uranium(VI) carbonato humate complex studied by cryo-TRLFS

    Energy Technology Data Exchange (ETDEWEB)

    Steudtner, R.; Sachs, S.; Schmeide, K.; Brendler, V.; Bernhard, G. [Helmholtz-Zentrum Dresden-Rossendorf, Dresden (Germany). Inst. of Radiochemistry

    2011-07-01

    The complex formation of U(VI) with humic acid (HA) in the presence of carbonate was studied by time-resolved laser-induced fluorescence spectroscopy at low temperature (cryo-TRLFS) at pH 8.5. In the presence of HA, a decrease of the luminescence intensity of U(VI) and no shift of the emission band maxima in comparison to the luminescence spectrum of the UO{sub 2}(CO{sub 3}){sub 3}{sup 4-} complex, the dominating U(VI) species under the applied experimental conditions in the absence of HA, was observed. The formation of a ternary U(VI) carbonato humate complex of the type UO{sub 2}(CO{sub 3}){sub 2}HA(II){sup 4-} starting from UO{sub 2}(CO{sub 3}){sub 3}{sup 4-} was concluded from the luminescence data. For this complex a complex stability constant of log K=2.83 {+-} 0.17 was determined. Slope analysis resulted in a slope of 1.12 {+-} 0.11, which verifies the postulated complexation reaction. The results agree very well with literature data. Speciation calculations show that the formation of the ternary U(VI) carbonato humate complex can significantly influence the U(VI) speciation under environmental conditions. (orig.)

  6. The uranium behaviour during rock-water interaction in the granites from the Itu complex (Sao Paulo, Brazil): a laboratory study

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Helen S.B. da; Marques, Leila S.; Kawauchi, Roberto K., E-mail: leila@iag.usp.br, E-mail: keiji@iag.usp.br [Instituto de Astronomia, Geofisica e Ciencias Atmosfericas. Universidade de Sao Paulo (USP), SP (Brazil)

    2011-07-01

    In order to elucidate the mechanisms involved in the process of uranium leaching due to the rock-water interaction in the granitic rocks from Itu Complex (Sao Paulo, Brazil), an experimental arrangement was developed and built. About 2.5kg of crushed rock fragments from Cabreuva and Indaiatuba Intrusions were maintained at room temperature within a glass flask filled with circulating water. The percolating water was removed periodically (from 10 to 30 days) for uranium analysis and then replaced by an equal volume of fresh water. Alpha spectrometry was used to determine the activity concentrations of {sup 234}U and {sup 238}U, and {sup 234}U/{sup 238}U activity ratios, of the waters as well as of the granites. The results for both samples showed that most of the uranium is leached in the first days after the contact between rock and water. The {sup 234}U/{sup 238}U activity ratios were significantly greater than unity, indicating radioactive disequilibrium between those isotopes, probably due to alpha recoil. Although the uranium activity concentrations in the water samples diminished with the increasing of time, it was not observed considerable variations of the {sup 234}U/{sup 238}U activity ratios. It was also noticed that, the amount of leached uranium as well as the {sup 234}U/{sup 238}U activity ratios are characteristics of each sample submitted to leaching, reflecting the differences of the granite facies mineralogy.(author)

  7. Estimation of the Pitzer equation parameters for aqueous complexes. A case study for uranium at 298.15 K and 1 atm

    International Nuclear Information System (INIS)

    Plyasunov, A.; Grenthe, I.; Fanghaenel, T.

    1998-01-01

    A procedure to estimate the Pitzer parameters for complexes or complex formation reactions from a small number of equilibrium constants (log K vs. I) obtained in 'constant ionic media' is discussed in some detail. It is then often impossible to determine both log K deg., the equilibrium constant at I=0, and all Pitzer parameters, hence some estimations or other simplifications are necessary. Solution coordination chemists have therefore preferred to use the less parametrized Broensted-Guggenheim-Scatchard (SIT) model. By comparison of analytical statements for the mean activity coefficients and equilibrium constants, for the SIT and Pitzer models we have shown that they are equivalent for ionic strengths less than 4 mol kg -1 , and have also established relationships between the Pitzer parameter β (1) and the charge type of the interacting ions, and between Δβ (1) for a complex formation reaction and ΔZETA 2 for the reaction, where ΔZETA 2 is the sum of the squared charges of the reactants/products with the proper stoichiometric coefficients. The first relationship is based on data in single electrolyte systems and the second on equilibrium-constant data determined in ionic media. For reactions involving species of charges one and two in 1-1 electrolyte ionic media we recommend the use of Δβ (1) /ΔZETA 2 = 0.337±0.014 kg mol -1 for the estimation of the Δβ (1) at 298.15 K and 1 atm. In this way we have used concentration equilibrium constant data to estimate log K deg. and Pitzer parameters β (0) and β (1) for more than 30 uranium complexes with other ions at 298.15 K and 1 atm. The procedure makes it possible to use the information on complex formation, acid/base and redox equilibria obtained in ionic media together with the Pitzer parameters for strong electrolytes for the modeling of complex equilibrium systems oer a broad range of ionic strength/ionic medium compositions, up to at least 4 mol kg -1 . (au)

  8. What a difference a 5f element makes: trivalent and tetravalent uranium halide complexes supported by one and two bis[2-(diisopropylphosphino)-4-methylphenyl]amido (PNP) ligands.

    Science.gov (United States)

    Cantat, Thibault; Scott, Brian L; Morris, David E; Kiplinger, Jaqueline L

    2009-03-02

    The coordination behavior of the bis[2-(diisopropylphosphino)-4-methylphenyl]amido ligand (PNP) toward UI3(THF)4 and UCl4 has been investigated to access new uranium(III) and uranium(IV) halide complexes supported by one and two PNP ligands. The reaction between (PNP)K (6) and 1 equiv of UI3(THF)4 afforded the trivalent halide complex (PNP)UI2(4-tBu-pyridine)2 (7) in the presence of 4-tert-butylpyridine. The same reaction carried out with UCl4 and no donor ligand gave [(PNP)UCl3]2 (8), in which the uranium coordination sphere in the (PNP)UCl3 unit is completed by a bridging chloride ligand. When UCl4 is reacted with 1 equiv (PNP)K (6) in the presence of THF, trimethylphosphine oxide (TMPO), or triphenylphosphineoxide (TPPO), the tetravalent halide complexes (PNP)UCl3(THF) (9), (PNP)UCl3(TMPO)2 (10), and (PNP)UCl3(TPPO) (11), respectively, are formed in excellent yields. The bis(PNP) complexes of uranium(III), (PNP)2UI (12), and uranium(IV), (PNP)2UCl2 (13), were easily isolated from the analogous reactions between 2 equiv of 6 and UI3(THF)4 or UCl4, respectively. Complexes 12 and 13 represent the first examples of complexes featuring two PNP ligands coordinated to a single metal center. Complexes 7-13 have been characterized by single-crystal X-ray diffraction and 1H and 31P NMR spectroscopy. The X-ray structures demonstrate the ability of the PNP ligand to adopt new coordination modes upon coordination to uranium. The PNP ligand can adopt both pseudo-meridional and pseudo-facial geometries when it is kappa3-(P,N,P) coordinated, depending on the steric demand at the uranium metal center. Additionally, its hemilabile character was demonstrated with an unusual kappa2-(P,N) coordination mode that is maintained in both the solid-state and in solution. Comparison of the structures of the mono(PNP) and bis(PNP) complexes 7, 9, 11-13 with their respective C5Me5 analogues 1-4 undoubtedly show that a more sterically congested environment is provided by the PNP ligand. The

  9. Chapter 6. Uranium extraction possibilities from natural uranium-bearing waters of complex salt composition. 6.2. Technology for uranium extraction from brine with a high content of ion-chlorine

    International Nuclear Information System (INIS)

    Khakimov, N.; Nazarov, Kh.M.; Mirsaidov, I.U.

    2012-01-01

    Present article is devoted to technology for uranium extraction from brine with a high content of ion-chlorine. The content of basic anions and cations in lake waters of Sasik-Kul deposit was defined. Results of X-ray spectral analysis of salt residual after water evaporation from Sasik-Kul lake was discussed. Investigations revealed that uranium extraction from brines containing ion-chlorine is possible. The developed basic process flow diagram of uranium extraction from Sasik-Kul Lake' brine consists of the following basic stages: evaporation, leaching, catching of formed gases (HCl), sorption, desorption, deposition, drying and tempering.

  10. Chapter 6. Uranium extraction possibilities from natural uranium-bearing waters of complex salt composition. 6.2. Technology for uranium extraction from brine with a high content of ion-chlorine

    International Nuclear Information System (INIS)

    Khakimov, N.; Nazarov, Kh.M.; Mirsaidov, I.U.

    2011-01-01

    Present article is devoted to technology for uranium extraction from brine with a high content of ion-chlorine. The content of basic anions and cations in lake waters of Sasik-Kul deposit was defined. Results of X-ray spectral analysis of salt residual after water evaporation from Sasik-Kul lake was discussed. Investigations revealed that uranium extraction from brines containing ion-chlorine is possible. The developed basic process flow diagram of uranium extraction from Sasik-Kul Lake' brine consists of the following basic stages: evaporation, leaching, catching of formed gases (HCl), sorption, desorption, deposition, drying and tempering.

  11. Spectroscopic investigations on sorption of uranium onto suspended bentonite. Effects of pH, ionic strength and complexing anions

    Energy Technology Data Exchange (ETDEWEB)

    Verma, Parveen Kumar; Pathak, Priyanath; Mohapatra, Manoj; Mohapatra, Prasanta Kumar [Bhabha Atomic Research Centre, Mumbai (India). Radiochemistry Div.; Yadav, Ashok Kumar; Jha, Sambhunath; Bhattacharyya, Dibyendu [Bhabha Atomic Research Centre, Mumbai (India). Atomic and Molecular Physics Div.

    2015-06-01

    Batch sorption experiments were carried out under aerobic conditions to understand the sorption behavior of U(VI) onto bentonite clay under varying pH (2-8) and ionic strength (I = 0.01 - 1 M (NaClO{sub 4})) conditions. The influences of different complexing anions (1 x 10{sup -4} M) such as oxalic acid (ox), carbonate (CO{sub 3}{sup 2-}), citric acid (cit), and humic acid (HA, 10 mg/L) on the sorption behavior were also investigated. The sorption of U(VI) increased with increasing pH up to pH 6 beyond which a decrease was attributed to the formation of anionic carbonate species. Marginal influence of the change in the ionic strength of the medium on the sorption profile of uranium suggested inner-sphere complexation onto the bentonite surface. The presence of humic acid showed interesting sorption profile with varying pH. Initially, there was an enhancement in the sorption with increased pH followed by a plateau and finally a decrease thereafter due to the formation of aqueous U(VI)-humate complexes. Spectroscopic studies such as UV spectrophotometry, luminescence and extended X-ray absorption fine structure (EXAFS) measurements were also performed to understand the changes in aqueous speciation of U(VI) ion. The luminescence yields of different aqueous U(VI) species followed the order: U(VI){sub Hydroxy} > U(VI){sub HumicAcid} > U(VI){sub carbonate} > U(VI){sub citrate}. The lower luminescence yield of U(VI)carbonate complex can be attributed to the strong dynamic quenching by carbonate at room temperature. The U(VI) samples shows two distinct life-time suggesting the presence of the different luminescent U(VI) species. Similar trend was observed for U(VI)-bentonite suspension in presence/absence of the complexing ligands. There was luminescence quenching for the sorbed U(VI) due to surface complexation. These observations were further supported by spectrophotometric measurements. EXAFS spectra of U(VI) samples were recorded in luminescence mode at the U L{sub 3

  12. Mixed complexes of uranium(IV) and thorium(IV) with N,N'-ethylenebis(salicylideneimine) and N,N'-propylenebis(salicylideneimine)

    Energy Technology Data Exchange (ETDEWEB)

    Doretti, L; Madalosso, F; Sitran, S; Faleschini, S [Consiglio Nazionale delle Ricerche, Padua (Italy). Lab. di Chimica e Tecnologia dei Radioelementi

    1976-01-01

    Recently some uranium tetrachloride adducts with N-(hydroxyphenyl)-salicylaldimine and N-(methoxyphenyl)salicylaldimine have been prepared (Doretti et al., J. Inorg. Nucl. Chem., (in press)): the study has now extended to the complexes of Uranium(IV) and Thorium(IV) with N,N'-Ethylenebis(salicylideneimine), H/sub 2/salen, and N,N'-Propylenebis(salicylideneimine), H/sub 2/salpropen, with the aim to prepare fully substituted complexes, mixed complexes containing both chloride and Schiff base groups and adducts of tetrachlorides with free Schiff bases. This paper reports the preparation and properties of the compounds MCl/sub 4/(H/sub 2/salen), MCl/sub 4/(H/sub 2/salpropen), M(salen)Cl/sub 2/, M(salen)/sub 2/ and M(salpropen)/sub 2/, where M = U or Th. These compounds have been characterized by elemental analyses and their IR spectra are reported and discussed.

  13. Studies on the extraction of uranium by N-octanoyl-N-phenylhydroxamic acid

    International Nuclear Information System (INIS)

    Saha, B.; Venkatesan, K.A.; Antony, M.P.; Vasudeva Rao, P.R.; Natarajan, R.

    2002-01-01

    N-octanoyl-N-phenylhydroxamic acid (OHA) has been prepared by partial reduction of nitrobenzene with Zn dust/NH 4 Cl, followed by acylation with n-octanoyl chloride. Structure of OHA was confirmed by 1 H NMR, IR spectra and CHNS microanalysis. The extraction of uranium by OHA has been studied as a function of pH, temperature and concentration of OHA. The extraction of uranium was found to increase with increase in pH. Uranium forms a 1 : 2 complex with OHA. IR Spectra and NMR Spectra of the uranium-OHA complex and slope analysis obtained from extraction studies indicated that the extraction of uranium was due to the formation of a chelate. The enthalpy change accompanied by the extraction of uranium by OHA has been obtained by temperature variation method. The extraction process was found to be endothermic at pH 2 and exothermic at pH 6. (orig.)

  14. Simultaneous precipitation of the carbonato complexes of uranium and plutonium by cationic surfactants

    International Nuclear Information System (INIS)

    Heckmann, K.; Strnad, J.

    1990-01-01

    Concerning the simultaneous precipitation of U and Pu or Th, preliminary experiments were made with various alkyl pyridinium salts and alkyl trimethyl ammonium salts to determine their precipitation properties with regard to carbonato and hydroxo complexes. The first experiments were made with cetyl pyridinium nitrate, with Th and U being precipitated from solutions with different carbonate concentrations. (DG) [de

  15. Isolation and structural characterization of uranium and other f block complexes with tridentate Schiff bases

    International Nuclear Information System (INIS)

    Singh, Kavita; Agarwala, B.V.

    1992-01-01

    Two Schiff base ligands, isatin semicarbazone(ISC) and o-vanillin salicyloylhydrazone(o-VSH) have been prepared and their complexes with U, La, Ce, Pr are synthesized and characterized by IR spectra, diffuse reflectance spectra, elemental analysis and other physico-chemical techniques. (author). 4 refs

  16. Efficient red organic electroluminescent devices based on trivalent europium complex obtained by designing the device structure with stepwise energy levels

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Liang; Jiang, Yunlong; Cui, Rongzhen; Li, Yanan; Zhao, Xuesen; Deng, Ruiping; Zhang, Hongjie, E-mail: hongjie@ciac.ac.cn

    2016-02-15

    In this study, we aim to further enhance the electroluminescence (EL) performances of trivalent europium complex Eu(TTA){sub 3}phen (TTA=thenoyltrifluoroacetone and phen=1,10-phenanthroline) by designing the device structure with stepwise energy levels. The widely used bipolar material 2,6-bis(3-(9H-carbazol-9-yl)phenyl)pyridine (26DCzPPy) was chosen as host material, while the doping concentration of Eu(TTA){sub 3}phen was optimized to be 4%. To facilitate the injection and transport of holes, MoO{sub 3} anode modification layer and 4,4′,4′′-Tris(carbazole-9-yl)triphenylamine (TcTa) hole transport layer were inserted in sequence. Efficient pure red emission with suppressed efficiency roll-off was obtained attributed to the reduction of accumulation holes, the broadening of recombination zone, and the improved balance of holes and electrons on Eu(TTA){sub 3}phen molecules. Finally, the device with 3 nm MoO{sub 3} and 5 nm TcTa obtained the highest brightness of 3278 cd/m{sup 2}, current efficiency of 12.45 cd/A, power efficiency of 11.50 lm/W, and external quantum efficiency of 6.60%. Such a device design strategy helps to improve the EL performances of emitters with low-lying energy levels and provides a chance to simplify device fabrication processes. - Highlights: • Electroluminescent performances of europium complex were further improved. • Device structure with stepwise energy levels was designed. • Better carriers' balance was realized by improving the injection and transport of holes. • The selection of bipolar host caused the broadening of recombination zone.

  17. Determination of traces of uranium in sea water after separation by froth flotation

    International Nuclear Information System (INIS)

    Sekine, K.

    1975-01-01

    Uranium in sea water is separated by froth flotation of the uranium (VI)-Arsenazo III-Zephiramine ion-adduct and then determined by neutron activation or spectrophotometric method using the uranium(IV)-Arsenazo III complex. Results of the analysis of Pacific coastal samples by the two methods are in good agreement; an average value of 3.0μg U/per liter was obtained. (author)

  18. The efficacy of the supramolecular complexes of niclosamide obtained by mechanochemical technology and targeted delivery against cestode infection of animals.

    Science.gov (United States)

    Arkhipov, Ivan A; Sadov, Konstantin M; Limova, Yulia V; Sadova, Alexandra K; Varlamova, Anastasiya I; Khalikov, Salavat S; Dushkin, Alexandr V; Chistyachenko, Yulia S

    2017-11-15

    Niclosamide is an anthelmintic that is widely used to treat cestode infection of animals. The efficacy of the supramolecular complexes of niclosamide obtained by mechanochemical technology and targeted delivery was studied in hymenolepiosis of mice and monieziosis of sheep. The efficacy of new substances of niclosamide with polyvinylpyrrolidone polymer in different ratios (1:10; 1:5; 1:2) was determined by the results of helminthological necropsy of the small intestine of sheep and mice. Pre-treatment eggs per gram (EPG) were not significantly different (P>0.1) among groups. The controlled test was used to evaluate the efficacy. A high efficacy (>95% efficacy) of the supramolecular complexes of niclosamide with PVP (SCoNwPVP) was shown in different ratios (1:10; 1:5 and 1:2) at a dose of 20mg/kg of body weight at oral administration against Hymenolepis nana in mice and Moniezia expansa in sheep. Whereas the basic drug - substance of niclosamide was effective at a dose of 100mg/kg of b/w. No adverse effects of the drugs on animal health were detected during the study. Copyright © 2017 Elsevier B.V. All rights reserved.

  19. The study of complex equilibria of uranium(VI) with selenate

    International Nuclear Information System (INIS)

    Lubal, P.; Havel, J.

    1997-01-01

    Uranyl (M)-selenate (L) complex equilibria in solution were investigated by spectrophotometry in visible range and potentiometry by means of uranyl ion selective electrode. The formation ML and ML 2 species was proved and the corresponding stability constants calculated were: log β 1 = 1.57 6 ± 0.01 6 , log β 2 = 2.42 3 ± 0.01 3 (I 3.0 mol 1 -1 Na(ClO 4 , SeO 4 ) (spectrophotometry) at 298.2 K. Using potentiometry the values for infinite dilution (I → 0 mol 1 -1 ) were: log β 1 = 2.64 ± 0.01, log β 2 ≤ 3.4 at 298.2 K. Absorption spectra of the complexes were calculated and analysed by deconvolution technique. Derivative spectrophotometry for the chemical model determination has also been successfully applied. (author)

  20. Alkyne- and alkyl-tris(cyclopentadienyl) complexes of uranium(III)

    International Nuclear Information System (INIS)

    Foyentin, M.; Folcher, G.; Ephritkhine, M.

    1987-01-01

    Treatment of cp 3 U(THF) (1) (cp=eta-C 5 H 5 , THF=tetrahydrofuran) with diphenylacetylene affords the alkyne complex cp 3 U(Ph-C identical to C-Ph); (1) reacts with RLi (R = Me, Busup(n)) to give the alkyl compounds cp 3 URLi (3); hydrogenolysis of (3) in the presence of a terminal alkene R'(-H) leads to the formation of cp 3 UR'Li. (author)

  1. Surface complexation modeling of the effects of phosphate on uranium(VI) adsorption

    Energy Technology Data Exchange (ETDEWEB)

    Romero-Gonzalez, M.R.; Cheng, T.; Barnett, M.O. [Auburn Univ., AL (United States). Dept. of Civil Engeneering; Roden, E.E. [Wisconsin Univ., Madison, WI (United States). Dept. of Geology and Geophysics

    2007-07-01

    Previous published data for the adsorption of U(VI) and/or phosphate onto amorphous Fe(III) oxides (hydrous ferric oxide, HFO) and crystalline Fe(III) oxides (goethite) was examined. These data were then used to test the ability of a commonly-used surface complexation model (SCM) to describe the adsorption of U(VI) and phosphate onto pure amorphous and crystalline Fe(III) oxides and synthetic goethite-coated sand, a surrogate for a natural Fe(III)-coated material, using the component additivity (CA) approach. Our modeling results show that this model was able to describe U(VI) adsorption onto both amorphous and crystalline Fe(III) oxides and also goethite-coated sand quite well in the absence of phosphate. However, because phosphate adsorption exhibits a stronger dependence on Fe(III) oxide type than U(VI) adsorption, we could not use this model to consistently describe phosphate adsorption onto both amorphous and crystalline Fe(III) oxides and goethite-coated sand. However, the effects of phosphate on U(VI) adsorption could be incorporated into the model to describe U(VI) adsorption to both amorphous and crystalline Fe(III) oxides and goethite-coated sand, at least for an initial approximation. These results illustrate both the potential and limitations of using surface complexation models developed from pure systems to describe metal/radionuclide adsorption under more complex conditions. (orig.)

  2. Surface complexation modeling of the effects of phosphate on uranium(VI) adsorption

    International Nuclear Information System (INIS)

    Romero-Gonzalez, M.R.; Cheng, T.; Barnett, M.O.; Roden, E.E.

    2007-01-01

    Previous published data for the adsorption of U(VI) and/or phosphate onto amorphous Fe(III) oxides (hydrous ferric oxide, HFO) and crystalline Fe(III) oxides (goethite) was examined. These data were then used to test the ability of a commonly-used surface complexation model (SCM) to describe the adsorption of U(VI) and phosphate onto pure amorphous and crystalline Fe(III) oxides and synthetic goethite-coated sand, a surrogate for a natural Fe(III)-coated material, using the component additivity (CA) approach. Our modeling results show that this model was able to describe U(VI) adsorption onto both amorphous and crystalline Fe(III) oxides and also goethite-coated sand quite well in the absence of phosphate. However, because phosphate adsorption exhibits a stronger dependence on Fe(III) oxide type than U(VI) adsorption, we could not use this model to consistently describe phosphate adsorption onto both amorphous and crystalline Fe(III) oxides and goethite-coated sand. However, the effects of phosphate on U(VI) adsorption could be incorporated into the model to describe U(VI) adsorption to both amorphous and crystalline Fe(III) oxides and goethite-coated sand, at least for an initial approximation. These results illustrate both the potential and limitations of using surface complexation models developed from pure systems to describe metal/radionuclide adsorption under more complex conditions. (orig.)

  3. Uranium speciation in plants

    International Nuclear Information System (INIS)

    Guenther, A.; Bernhard, G.; Geipel, G.; Reich, T.; Rossberg, A.; Nitsche, H.

    2003-01-01

    Detailed knowledge of the nature of uranium complexes formed after the uptake by plants is an essential prerequisite to describe the migration behavior of uranium in the environment. This study focuses on the determination of uranium speciation after uptake of uranium by lupine plants. For the first time, time-resolved laser-induced fluorescence spectroscopy and X-ray absorption spectroscopy were used to determine the chemical speciation of uranium in plants. Differences were detected between the uranium speciation in the initial solution (hydroponic solution and pore water of soil) and inside the lupine plants. The oxidation state of uranium did not change and remained hexavalent after it was taken up by the lupine plants. The chemical speciation of uranium was identical in the roots, shoot axis, and leaves and was independent of the uranium speciation in the uptake solution. The results indicate that the uranium is predominantly bound as uranyl(VI) phosphate to the phosphoryl groups. Dandelions and lamb's lettuce showed uranium speciation identical to lupine plants. (orig.)

  4. Chemical thermodynamics of uranium

    International Nuclear Information System (INIS)

    Grenthe, I.; Fuger, J.; Lemire, R.J.; Muller, A.B.; Nguyen-Trung Cregu, C.; Wanner, H.

    1992-01-01

    A comprehensive overview on the chemical thermodynamics of those elements that are of particular importance in the safety assessment of radioactive waste disposal systems is provided. This is the first volume in a series of critical reviews to be published on this subject. The book provides an extensive compilation of chemical thermodynamic data for uranium. A description of procedures for activity corrections and uncertainty estimates is given. A critical discussion of data needed for nuclear waste management assessments, including areas where significant gaps of knowledge exist is presented. A detailed inventory of chemical thermodynamic data for inorganic compounds and complexes of uranium is listed. Data and their uncertainty limits are recommended for 74 aqueous complexes and 199 solid and 31 gaseous compounds containing uranium, and on 52 aqueous and 17 solid auxiliary species containing no uranium. The data are internally consistent and compatible with the CODATA Key Values. The book contains a detailed discussion of procedures used for activity factor corrections in aqueous solution, as well as including methods for making uncertainty estimates. The recommended data have been prepared for use in environmental geochemistry. Containing contributions written by experts the chapters cover various subject areas such a s: oxide and hydroxide compounds and complexes, the uranium nitrides, the solid uranium nitrates and the arsenic-containing uranium compounds, uranates, procedures for consistent estimation of entropies, gaseous and solid uranium halides, gaseous uranium oxides, solid phosphorous-containing uranium compounds, alkali metal uranates, uncertainties, standards and conventions, aqueous complexes, uranium minerals dealing with solubility products and ionic strength corrections. The book is intended for nuclear research establishments and consulting firms dealing with uranium mining and nuclear waste disposal, as well as academic and research institutes

  5. A comparative study between the dissolution and the leaching methods for the separation of rare earths, uranium and thorium from hydrous metal oxide cake obtained by the alkaline digestion of monazite

    International Nuclear Information System (INIS)

    Chayavadhanangkur, C.; Busamongkol, A.; Hongsirinirachorn, S.; Rodthongkom, C.; Sirisena, K.

    1986-12-01

    Methods for the group-separation of rare-earths, thorium and uranium from hydrous metal oxide cake obtained by the alkaline digestion of monazite were studied. Leaching of the hydrous metal oxide cake at pH between 4-5 separates the elements under investigation into 3 major groups which are suitable to be used as feed materials for further purification. Total dissolution and gradient precipitation at pH 4-5 yields a poorer separation in comparison to the leaching method

  6. Mono-, di- and trinuclear dioxo complexes of uranium containing hydrazonato and azomethine ligands

    International Nuclear Information System (INIS)

    Gatto, C.C.; Schulz Lang, E.

    2004-01-01

    Mono-, di or trinuclear dioxouranium complexes with benzoylhydrazonato or azomethine ligands were prepared by reactions of common dioxouranium precursors such as UO 2 (NO 3 ) 2 . 6 H 2 O or [NBu 4 ] 2 [UO 2 Cl 4 ] with vanillin benzoylhydrazone (H 2 L 4 ), salicylaldehyde benzoylhydrazone (H 2 L 5 ), 2-hydroxyacetylbenzene salicylhydrazone (H 3 L 6 ) or N-(2-ethoxycarbonyl-3-oxo-but-1-en(1)yl)-2-aminophenol (H 2 L 7 ). Spectroscopic and X-ray crystallographic studies on the complexes [NBu 4 ] 2 [UO 2 Cl 4 ] . 2 H 2 L 4 , [UO 2 (HL 5 )(H 2 L 5 ) 2 ](NO 3 ), [HNEt 3 ] 2 [{UO 2 (L 6 )} 2 ] and [HNEt 3 ] 2 [{UO 2 (L 7 } 3 O)] confirm that the individual donor atom constellation, the size of the potential chelate rings and the acidity of the OH and NH functionalities of the proligands have a strong influence on the structure of the products. (Abstract Copyright [2004], Wiley Periodicals, Inc.) [de

  7. Triamidoamine-uranium(IV)-stabilized terminal parent phosphide and phosphinidene complexes

    Energy Technology Data Exchange (ETDEWEB)

    Gardner, Benedict M.; McMaster, Jonathan; Lewis, William; Blake, Alexander J.; Liddle, Stephen T. [School of Chemistry, University of Nottingham (United Kingdom); Balazs, Gabor; Scheer, Manfred [Institut of Inorganic Chemistry, University of Regensburg (Germany); Tuna, Floriana; McInnes, Eric J.L. [School of Chemistry and Photon Science Institute, University of Manchester (United Kingdom)

    2014-04-22

    Reaction of [U(Tren{sup TIPS})(THF)][BPh{sub 4}] (1; Tren{sup TIPS}=N{CH_2CH_2NSi(iPr)_3}{sub 3}) with NaPH{sub 2} afforded the novel f-block terminal parent phosphide complex [U(Tren {sup TIPS})(PH{sub 2})] (2; U-P=2.883(2) Aa). Treatment of 2 with one equivalent of KCH{sub 2}C{sub 6}H{sub 5} and two equivalents of benzo-15-crown-5 ether (B15C5) afforded the unprecedented metal-stabilized terminal parent phosphinidene complex [U(Tren{sup TIPS})(PH)][K(B15C5){sub 2}] (4; U=P=2.613(2) Aa). DFT calculations reveal a polarized-covalent U=P bond with a Mayer bond order of 1.92. (copyright 2014 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  8. Investigation of quantitative separation of thorium, uranium, neptunium and plutonium from complex radiochemical mixtures

    International Nuclear Information System (INIS)

    Ushatskij, V.N.; Preobrazhenskaya, L.D.; Kolychev, V.B.; Gugel', E.S.

    1979-01-01

    Quantitative separation of actinides and their radiochemical purification with the aid of TBP with subsequent separation of thorium and quantitative separation of U, Np and Pu with the aid of D2EHPA have been studied. The method has been developed for quantitative extraction-chromatographic separation and radiochemical purification of nanogram amounts of U, Pu and microgram amounts of Th and Np from complex radiochemical mixtures containing both fragment radioisotopes and non-radioactive macrocomponents ( Fe,Al,Mg,Mn, Na and others). The method calls for application of one-extraction-chromatographic column with TBP and one column with D2EHPA. Thorium is separated at the first stage since it does not form complexes in a chloride solution during washing of the sorption column with 6. OM HCl. Npsup((4)) and Pusup((3)) required for separation are stabilized with the aid of hydrazine and hydroxylamine mixture. The yield of each of the above-cited actinide elements during the complete two-stage separation and at the stage of their separation varies within the range of 98.5-99.3%

  9. Improved fluorimetric measurement of uranium uptake and distribution in spring wheat (Triticum aestivum L.)

    Energy Technology Data Exchange (ETDEWEB)

    Borcia, Catalin [' ' Alexandru Ioan Cuza' ' Univ., Iasi (Romania). Dept. of Physics; Popa, Karin; Cecal, Alexandru [' ' Alexandru Ioan Cuza' ' Univ., Iasi (Romania). Dept. of Chemistry; Murariu, Manuela [' ' Petru Poni' ' Institute of Macromolecular Chemistry, Iasi (Romania)

    2016-08-01

    Uranium uptake and (radio)toxicity was tested on spring wheat (Triticum aestivum L.) in a laboratory study using differently concentrated uranium nitrate solutions. Within these experiments, two analytical assays of uranium were comparatively tested: a fast and improved fluorimetric assay and the classical colorimetric (U(IV)-arsenazo(III) complexation) one. During the germination, the wheat seeds and plantlets supported well the uranium solutions of treatment within the entire concentration range (1 x 10{sup -4} -5 x 10{sup -3} M). Uranium proved to be non (radio)toxic to wheat as compared with other natural and anthropogenic radiocations, probably because its uptake by spring wheat during the germination is low. Indeed, only a small fraction of uranium administered was located within the roots, whereas the uranium content of the stems was negligible. A high correlation between the results obtained by two analytical methods was found. However, the fluorimetric assay proved to be more reliable and fast, and accurate.

  10. Near-field high-temperature transport: Evidence from the genesis of the Osamu Utsumi uranium mine, Pocos de Caldas alkaline complex, Brazil

    International Nuclear Information System (INIS)

    Cathles, L.M.; Shea, M.E.

    1990-01-01

    The chemical, isotopic and mineralogical alteration which occurred during primary uranium ore deposition at the breccia pipe-hosted Osamu Utsumi mine, Pocos de Caldas, Brazil, was studied as a natural analogue for near-field radionuclide migration. Chemical and isotopic alteration models were combined with finite difference models of the convective cooling of caldera intrusives. Application of the chemical models successfully used to interpret mineralization and alteration at the Osamu Utsumi mine to the hypothetical waste repository shows that even in a worst case scenario (waste emplaced in a permeable host rock with no measures taken to inhibit flow through the repository), the amount of hydrothermal alteration in the hypothetical repository will be about 0.1% of that in the breccia pipe at the Osamu Utsumi mine. Assuming no barriers to uranium mobility, uranium precipitation above the hypothetical repository would be 0.05 ppm (rather than 50 ppm), hydrothermal alteration 0.03 wt.% (rather than 30 wt.%), etc. The analysis indicates that mineralogical alteration is extremely sensitive to thermodynamic data. Prediction of mineralogical alteration (which may be necessary to predict the migration of radionuclides other than uranium, for example) probably cannot be based directly on even very carefully collected laboratory thermodynamic data. Mineralogical complexities of the system, as well as database uncertainties, will require calibration of the thermodynamic framework against mineralogical alteration observed in the laboratory or field by procedures briefly described. (au)

  11. Activation of CO{sub 2} and related small molecules by neopentyl-derivatized uranium complexes

    Energy Technology Data Exchange (ETDEWEB)

    Schmidt, Anna-Corina

    2015-06-18

    This work reports the newly synthesized neopentyl derivatized tris(aryloxide) U{sup III} complex [(({sup nP,Me}ArO){sub 3}tacn)U{sup III}] (1) and its reactivity with small molecules like nitrous oxide (N{sub 2}O), carbon dioxide (CO{sub 2}), and sulfur dioxide (SO{sub 2}). Additionally, a deeper insight into covalency of U-R bonds with R = O, N and the participation of the f-orbitals to bonding are discussed. For this purpose, a large number of characterization methods were used, such as X-ray diffraction analysis, U{sup V}/vis/NIR, IR vibrational, Raman, X-ray absorption, EPR, and {sup 1}H, {sup 15}N, {sup 13}C and {sup 19}F NMR spectroscopy, cyclic voltammetry, SQUID magnetization measurements and DFT calculations. Moreover, all compounds were checked for purity by elemental analysis.

  12. Complexation modelling of uranium and other actinides by organic compounds of natural or synthetic origin

    International Nuclear Information System (INIS)

    Bouby, M.

    1998-01-01

    The future of nuclear wastes raises a lot of questions. Their resolution require an accurate knowledge of the physical, chemical and biological processes which affect the properties of radioelements constituting the wastes. 3 research themes have been approached. The experimental methods used are: neutronic activation analysis, UV-visible spectrophotometry and time-resolved induced laser spectro-fluorimetry. A part of the phenomena has been modelled by ionic strength correction models (as Davies or MSA). The main results have revealed: 1)the bio-sorption capacities of the microorganism (Mycobacterium phlei) for UO 2 2+ and NpO 2+ (in conditions where the specific adsorption capacities Qe(UO 2 2+ )=60 and Qe(NpO 2+ )=444 moles cations/g dry biomass 2)the retention capacities, in various leaching conditions, by this bacteria of the ions initially adsorbed 3)the complexation properties of 2 siderophores for the cations UO 2 2+ , U 4+ and Th 4+ . The thermodynamical equilibrium constants were determined for one of the siderophore: the pyoverdine A; they were such that KUO 2 2+ ≤KU 4+ ≤KTh 4+ 4)in very acidic media (HCl and HClO 4 until 12 M), the behaviour of the acylisoxazolone HPBI (1-phenyl-4-benzoyl-5-isoxazolone) and the value of its acidity thermodynamical constant is such that 0.13≤KATh≤0.32 at 25 degrees Celsius 5)the variations of the fluorescence properties of the uranyl cation in terms of the acidity of the concentrated media (HClO 4 and CF 3 SO 3 H) in which they are in solution; it seems that a complexation between the uranyl ion and the counter-ions present in solution occur. (O.M.)

  13. Spectrophotometric determination of trace uranium in phosphate ore samples from kurum and uro areas, Nuba mountains, Sudan

    International Nuclear Information System (INIS)

    Mohamed, A. A.; Ali, A. H.; Altayeb, M. A. H.

    2004-01-01

    A method was proposed for the spectrophotometric determination of uranium content in phosphate ores. the method is based on the use of nitrogen (v) acid for leaching the rock, and treatment with ammonium carbonate solution, whereby uranium (Vi) is kept in solution as its carbonate complex. The ion-exchange technique was used for the recovery of uranium. Uranium was determined spectrophotometrically by measurement of the absorbance of the yellow uranium (Vi)-8-hydroxyquinolate complex at λ 425 nm. The procedure was used for the determination of trace uranium content in 30 phosphate ore samples collected from Kurun and Uro areas in Nuba mountains in Sudan. X-ray fluorescence technique was employed for the assessment of the method used. The spectrophotometric method results show a high similarity with those obtained by XRF technique. This agreement indicates that the procedure proposed here has been successfully applied for the determination of uranium in phosphate ores. (Author)

  14. Crystal structure of importin-{alpha} complexed with a classic nuclear localization sequence obtained by oriented peptide library screening

    Energy Technology Data Exchange (ETDEWEB)

    Takeda, A.A.S.; Fontes, M.R.M. [UNESP, Universidade Estadual Paulista, Botucatu, SP (Brazil); Yang, S.N.Y. [University of Melbourne, Melbourne (Australia); Harris, J.M. [Queensland University of Technology, Brisbane (Australia); Jans, D.A. [Monash University, Clayton (Australia); Kobe, B. [University of Queensland, Brisbane, QU (Australia)

    2012-07-01

    Full text: Importin-{alpha} (Imp{alpha}) plays a role in the classical nuclear import pathway, binding to cargo proteins with activities in the nucleus. Different Imp{alpha} paralogs responsible for specific cargos can be found in a single organism. The cargos contain nuclear localization sequences (NLSs), which are characterized by one or two clusters of basic amino acids (monopartite and bipartite NLSs, respectively). In this work we present the crystal structure of Imp{alpha} from M. musculus (residues 70-529, lacking the auto inhibitory domain) bound to a NLS peptide (pepTM). The peptide corresponds to the optimal sequence obtained by an oriented peptide library experiment designed to probe the specificity of the major NLS binding site. The peptide library used five degenerate positions and identified the sequence KKKRR as the optimal sequence for binding to this site for mouse Imp{alpha} (70-529). The protein was obtained using an E. coli expression system and purified by affinity chromatography followed by an ion exchange chromatography. A single crystal of Imp{alpha} -pepTM complex was grown by the hanging drop method. The data were collected using the Synchrotron Radiation Source LNLS, Brazil and processed to 2.3. Molecular replacement techniques were used to determine the crystal structure. Electron density corresponding to the peptide was present in both major and minor binding sites The peptide is bound to Imp{alpha} similar as the simian virus 40 (SV40) large tumour (T)-antigen NLS. Binding assays confirmed that the peptide bound to Imp{alpha} with low nM affinities. This is the first time that structural information has been linked to an oriented peptide library screening approach for importin-{alpha}; the results will contribute to understanding of the sequence determinants of classical NLSs, and may help identify as yet unidentified classical NLSs in novel proteins. (author)

  15. Contribution to the study of gaseous Carburization of Uranium

    International Nuclear Information System (INIS)

    Esteban Hernandez, J. A.; Jimenez Moreno, J. M.; Villota Ruiz, P. de

    1966-01-01

    Thermal decomposition of uranium hydride powder obtained by hydrogenation of uranium turnings is studied on the first part of this paper. Carburization of the uranium hydride or metallic uranium powder with methane is studied in the second part. A method of uranium monocarbide fabrication under static atmosphere is described. On this method hydrogen is removed by means of an uranium getter. (Author) 6 refs

  16. Surface complexation modeling of uranium (Vi) retained onto zirconium diphosphate in presence of organic acids

    International Nuclear Information System (INIS)

    Almazan T, M. G.; Garcia G, N.; Ordonez R, E.

    2010-10-01

    In the field of nuclear waste disposal, predictions regarding radionuclide migration through the geosphere, have to take account the effects of natural organic matter. This work presents an investigation of interaction mechanisms between U (Vi) and zirconium diphosphate (ZrP 2 O 7 ) in presence of organic acids (citric acid and oxalic acid). The retention reactions were previously examined using a batch equilibrium method. Previous results showed that U (Vi) retention was more efficient when citric acid or oxalic acid was present in solid surface at lower ph values. In order to determine the retention equilibria for both systems studied, a phosphorescence spectroscopy study was carried out. The experimental data were then fitted using the Constant Capacitance Model included in the FITEQL4.0 code. Previous results concerning surface characterization of ZrP 2 O 7 (surface sites density and surface acidity constants) were used to constraint the modeling. The best fit for U (Vi)/citric acid/ZrP 2 O 7 and U (Vi)/oxalic acid/ZrP 2 O 7 systems considered the formation of a ternary surface complex. (Author)

  17. Uranium extraction from underground deposits

    International Nuclear Information System (INIS)

    Wolfe, C.R.

    1982-01-01

    Uranium is extracted from underground deposits by passing an aqueous oxidizing solution of carbon dioxide over the ore in the presence of calcium ions. Complex uranium carbonate or bicarbonate ions are formed which enter the solution. The solution is forced to the surface and the uranium removed from it

  18. A Solution to Modeling Multilevel Confirmatory Factor Analysis with Data Obtained from Complex Survey Sampling to Avoid Conflated Parameter Estimates

    Directory of Open Access Journals (Sweden)

    Jiun-Yu Wu

    2017-09-01

    Full Text Available The issue of equality in the between-and within-level structures in Multilevel Confirmatory Factor Analysis (MCFA models has been influential for obtaining unbiased parameter estimates and statistical inferences. A commonly seen condition is the inequality of factor loadings under equal level-varying structures. With mathematical investigation and Monte Carlo simulation, this study compared the robustness of five statistical models including two model-based (a true and a mis-specified models, one design-based, and two maximum models (two models where the full rank of variance-covariance matrix is estimated in between level and within level, respectively in analyzing complex survey measurement data with level-varying factor loadings. The empirical data of 120 3rd graders' (from 40 classrooms perceived Harter competence scale were modeled using MCFA and the parameter estimates were used as true parameters to perform the Monte Carlo simulation study. Results showed maximum models was robust to unequal factor loadings while the design-based and the miss-specified model-based approaches produced conflated results and spurious statistical inferences. We recommend the use of maximum models if researchers have limited information about the pattern of factor loadings and measurement structures. Measurement models are key components of Structural Equation Modeling (SEM; therefore, the findings can be generalized to multilevel SEM and CFA models. Mplus codes are provided for maximum models and other analytical models.

  19. Contribution to uranium geochemistry in intrusive granites

    International Nuclear Information System (INIS)

    Coulomb, R.

    1959-01-01

    This work aims to define the position of a certain number of French granitic deposits within the field of the geochemistry of granites in general, and of the geochemistry of uranium in particular. The regions concerned are: - 3 French Hercynian ranges, in the Vendee, in Brittany and in the Morvan, - 1 African range, probably precambrian, of the Hoggar. For each range, the petrochemical framework is first of all determined and then the degree of chemical homogeneity of the rocks is evaluated. In the petrochemical groups thus obtained the geochemical behaviour of the uranium is studied. From a point of view of the geochemistry of the granites under investigation, a comparison of the laws of distribution of the major elements in the 4 ranges shows up a convergence of average composition which was not anticipated by geological and petrographic considerations alone. The statistical and geochemical distribution laws of the total uranium as a function of the petrochemical variations are established. A study of the chemical forms of uranium in the rocks has drawn an attention to the qualitative and quantitative importance of the fraction of this uranium soluble in dilute acids. We have therefore reconsidered on the one hand, the laws of distribution of the insoluble uranium, which represents essentially the uranium fixed in crystalline structures (zircon, allanite...), and we have justified on the other hand the interest presented by the soluble uranium: this, although more complex in character, presents a geochemical unity in post magmatic phenomena which makes possible to find a genetic connection between the uraniferous deposits and the intrusive massifs. Finally we have given a plan of the geochemical cycle of uranium, in which we hope to have provided some more accurate data on the igneous phase. (author) [fr

  20. Uranium mining

    International Nuclear Information System (INIS)

    Cheeseman, E.W.

    1980-01-01

    The international uranium market appears to be currently over-supplied with a resultant softening in prices. Buyers on the international market are unhappy about some of the restrictions placed on sales by the government, and Canadian sales may suffer as a result. About 64 percent of Canada's shipments come from five operating Ontario mines, with the balance from Saskatchewan. Several other properties will be producing within the next few years. In spite of the adverse effects of the Three Mile Island incident and the default by the T.V.A. of their contract, some 3 600 tonnes of new uranium sales were completed during the year. The price for uranium had stabilized at US $42 - $44 by mid 1979, but by early 1980 had softened somewhat. The year 1979 saw the completion of major environmental hearings in Ontario and Newfoundland and the start of the B.C. inquiry. Two more hearings are scheduled for Saskatchewan in 1980. The Elliot Lake uranium mining expansion hearings are reviewed, as are other recent hearings. In the production of uranium for nuclear fuel cycle, environmental matters are of major concern to the industry, the public and to governments. Research is being conducted to determine the most effective method for removing radium from tailings area effluents. Very stringent criteria are being drawn up by the regulatory agencies that must be met by the industry in order to obtain an operating licence from the AECB. These criteria cover seepages from the tailings basin and through the tailings retention dam, seismic stability, and both short and long term management of the tailings waste management area. (auth)

  1. Depleted uranium

    International Nuclear Information System (INIS)

    Huffer, E.; Nifenecker, H.

    2001-02-01

    This document deals with the physical, chemical and radiological properties of the depleted uranium. What is the depleted uranium? Why do the military use depleted uranium and what are the risk for the health? (A.L.B.)

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

    International Nuclear Information System (INIS)

    Monteillet, A.

    1985-02-01

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

  3. Uranium ore waste management of the CIPC (Mining Industrial Complex of Pocos de Caldas Plateau, Minas Gerais State, Brazil)

    International Nuclear Information System (INIS)

    Wiikmann, Luiz Oide; Figueiredo, Nestor; Taddei, Jose Fernando Aguiar Carrazedo; Valente, Sergio Mozart Coutinho; Chilelli Junior, Vicente; Souza, Vicente Paulo de

    1995-01-01

    Since 1982, the facilities in CIPC has been producing a uranium concentrate under ammonium diuranate form, from uranium ore. The CIPC,s Waste Management System is responsible for monitoring and controlling the mining and milling effluents, in accordance with norms established by government regulatory agencies. Here we are concerned with this system's efficiency, costs and, with necessary procedures for waste rock piles'stabilization in physical, chemical and biological aspects with aim of environmentally restoring these areas. (author). 2 refs., 6 figs., 5 tabs

  4. Vaal Reefs South uranium plant

    International Nuclear Information System (INIS)

    Anon.

    1979-01-01

    The Vaal Reefs mining complex, part of the Anglo American Corporation, is the largest gold and uranium producing complex in the world, being South Africa's principal producer, accounting for about a quarter of the country's uranium production. Vaal Reefs South uranium plant in the Orkney district was recently officially opened by Dr AJA Roux, the retiring president of the Atomic Energy Board and chairman of the Uranium Enrichment Corporation and will increase the country's uranium production. In the field of technology, and particularly processing technology, South Africa has shown the world unprecedented technology achievement in the field of uranium extraction from low grade ores and the development of the unique uranium enrichment process. New technical innovations that have been incorporated in this new plant are discussed

  5. Formation of Aqueous MgUO2(CO3)32- Complex and Uranium Anion Exchange Mechanism onto an Exchange Resin

    International Nuclear Information System (INIS)

    Dong, Wenming; Brooks, Scott C

    2008-01-01

    The formation of and stability constants for aqueous Mg-UO2-CO3 complexes were determined using an anion exchange method. Magnesium concentration was varied (up to 20 mmol/L) at constant ionic strength (I = 0.101, 0.202, 0.304, 0.406, and 0.509 mol/kg NaNO3), pH = 8.1, total [U(VI)] = 10.4 mol/L under equilibrium with atmospheric CO2. The results indicate that only the MgUO2(CO3)32- complex is formed. The cumulative formation constant extrapolated to zero ionic strength is similar regardless of the activity correction convention used: log = 25.8 b 0.5 using Davies equation and = 25.02 b 0.08 using specific ion interaction theory (SIT). Uranium sorption onto the exchange resin decreased in the presence of Mg putatively due to the formation of MgUO2(CO3)32- that had a lower affinity for the resin than UO2(CO3)34-. Uranium sorption results are consistent with an equivalent anion exchange reaction between NO3- and UO2(CO3)34- species to retain charge neutrality regardless of Mg concentration. No Mg was associated with the anion exchange resin indicating that the MgUO2(CO3)32- complex did not sorb

  6. Discovery of uranium mineralizations in the rhyolite-granite complex in the Jabal Eghei area of southern Libya

    Directory of Open Access Journals (Sweden)

    Kovačević Jovan

    2013-01-01

    Full Text Available During investigation of the Jabal Eghei area in southern Libya and the production of geological maps at a scale of 1:250 000 (Tibesti sector, sheet Wadi Eghei NF 34-1 and NF 34-2, regional prospecting for mineral raw materials was performed. Radiometric survey of observed targets at the sites indicated two significant uranium mineralizations in rhyolites, and some smaller ones in granites that are in close contact with rhyolites. Rhyolites are located in the central part of the investigated region. They cut through granite rocks. The first mineralization is in the central part of the rhyolite region, which is mostly composed of silificated rhyolites. The second one was discovered near the granite-rhyolite contact zone, characterized by the presence of silicified breccia rocks. These findings were confirmed by laboratory measurements of more than seventy samples collected in the area, using high resolution gamma-ray spectrometry. The concentrations of uranium in these mineralizations were found to range from approx. 50 mg kg-1 to more than 600 mg kg-1. The latter value is about 240 times above the Earth’s average. Besides uranium, these measurements have also given concentrations of thorium and potassium. Additional geochemical analysis was performed on samples taken from locations where uranium anomalies were discovered using ICP-MS technique, in which concentrations of more than forty elements were determined. Uranium mineralizations are accompained by increased contents of silver (up to 17 times, arsenic (up to 8 times, molybdenum (up to 50 times, mercury (up to 9 times, and lead (up to 14 times, in regard to the Clark’s values. These results warrant a continued investigation of this region because of potential interest in the discovery of nuclear mineral raw materials.

  7. Uranium conversion

    International Nuclear Information System (INIS)

    Oliver, Lena; Peterson, Jenny; Wilhelmsen, Katarina

    2006-03-01

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

  8. Uranium exploration

    International Nuclear Information System (INIS)

    De Voto, R.H.

    1984-01-01

    This paper is a review of the methodology and technology that are currently being used in varying degrees in uranium exploration activities worldwide. Since uranium is ubiquitous and occurs in trace amounts (0.2 to 5 ppm) in virtually all rocks of the crust of the earth, exploration for uranium is essentially the search of geologic environments in which geologic processes have produced unusual concentrations of uranium. Since the level of concentration of uranium of economic interest is dependent on the present and future price of uranium, it is appropriate here to review briefly the economic realities of uranium-fueled power generation. (author)

  9. Uranium and lanthanide complexes with the 2-mercapto benzothiazolate ligand: Evidence for a specific covalent binding site in the differentiation of isostructural lanthanide(III) and actinide(III) compounds

    Energy Technology Data Exchange (ETDEWEB)

    Roger, M.; Arliguie, T.; Thuery, P.; Ephritikhine, M. [CEA Saclay, DSM, DRECAM, Serv Chim Mol, CNRS URA 331, F-91191 Gif Sur Yvette, (France); Belkhiri, L. [Univ Mentouri Constantine, Fac Sci, Dept Chim, Lab Chim Mol LACMOM, Constantine 25017, (Algeria); Boucekkine, A. [Univ Rennes 1, CNRS, UMR Sci Chim Rennes 6226, F-35042 Rennes, (France)

    2008-07-01

    Treatment Of [U(Cp*){sub 2}Cl{sub 2}] with KSBT in THF gave [U(Cp*){sub 2}(SBT){sub 2}], which exhibits the usual bent sandwich configuration in the solid state with the two SBT ligands adopting the bidentate ligation mode. The mono-cyclopentadienyl compound [U(Cp*)(SBT){sub 3}] was synthesized by reaction of [U(Cp*)(BH{sub 4}){sub 3}] with KSBT in THF, and its reduction with potassium amalgam in the presence of 18-crown-6 afforded the corresponding anionic complex [K(18-crown-6)(THF){sub 2}][U(Cp*)(SBT){sub 3}]. The lanthanide analogues [K(THF){sub 2}Ln(Cp*)(SBT){sub 3}] were obtained by treating [Ln(BH{sub 4}){sub 3}(THF){sub 3}] with KSBT and KCp*; isomorphous crystals of [K(15-crown-5){sub 2}] [Ln(Cp*)(SBT){sub 3}].THF [Ln = La, Ce, Nd] were formed upon addition of 15-crown-5. Comparison of the crystal structures of the pentagonal bipyramidal complexes [M(Cp*)(SBT){sub 3}]{sup -} reveals that the M-Nax distances are shorter than the M-Neq distances, whatever the metal, the phenomenon being enhanced in the U(III) compound versus the Ln(III) analogues. The structural data obtained by relativistic density functional theory (DFT) calculations reproduce experimental trends. Electronic population and molecular orbital analyses show that the structural differences in the series of [M(Cp*)(SBT){sub 3}]{sup -} anions are related to the uranium 5f orbital-ligand mixing, which is greater than the lanthanide 4f orbital-ligand mixing. Moreover, the consideration of the corresponding bond orders and the analysis of the bonding energy bring to light a strong and specific interaction between the uranium and apical nitrogen atoms. (authors)

  10. How much complexity is warranted in a rainfall-runoff model? Findings obtained from symbolic regression, using Eureqa

    Science.gov (United States)

    Abrahart, R. J.; Beriro, D. J.

    2012-04-01

    The information content in a rainfall-runoff record is sufficient to support models of only very limited complexity (Jakeman and Hornberger, 1993). This begs the question of what limits should observed data place on the allowable complexity of rainfall-runoff models? Eureqa1 (Schmidt and Lipson, 2009) - pronounced "eureka" - is a software tool for finding equations and detecting mathematical relationships in a dataset. The challenge, for both software and modeller, is to identify, by means of symbolic regression, the simplest mathematical formulas which describe the underlying mechanisms that produced the data. It actually delivers, however, a series of preferred modelling solutions comprising one champion for each specific level of complexity i.e. related to solution enlargement involving the progressive incorporation of additional permitted factors (internal operators/ external drivers). The potential benefit of increased complexity can as a result be assessed in a rational manner. Eureqa is free to download and use; and, in the current study, has been employed to construct a set of rainfall-runoff transfer function models for the Annapolis River at Wilmot, in north-western Nova Scotia, Canada. The climatic conditions in this catchment present an interesting set of modelling challenges; daily variations and seasonal changes in temperature, snowfall and retention result in great difficulty for runoff prediction by means of a data-driven approach. Data from 10 years of daily observations are used in the present study (01/01/2000-31/12/2009): comprising [i] discharge, [ii] total rainfall (excluding snowfall), [iii] total snowfall, [iv] thickness of snow cover, and [v] maximum and [vi] minimum temperature. Precipitation occurs throughout the whole year being slightly lower during summer. Snowfall is common from November until April and rare hurricane weather may occur in autumn. The average maximum temperature is below 0 0C in January and February, but significant

  11. Spectrophotometric study of the complexation equilibria of uranium(VI) with 1,4-bis(4'-methylanilino)anthraquinone and determination of uranium(VI)

    International Nuclear Information System (INIS)

    Idriss, K.A.; Seleim, M.M.; Abu-Bakr, M.S.; Sedaira, H.

    1985-01-01

    The reaction of U(VI) with 1,4-bis(4'-methylanilino)anthraquinone (quinizarin green) in water-dimethylformamide medium was investigated spectrophotometrically. The complexation equilibria in solution were demonstrated. The study of the reaction in presence of equimolar concentrations or in solutions containing metal or ligand excess gave evidence for the formation of complexes with stoichiometric ratios of UO 2 :L = 1:1 and 1:2 in dependence on the pH of the medium. Their thermodynamic stabilities and the values of their molar absorption coefficients were determined. The optimum conditions for spectrophotometric determination of U(VI) with this reagent were found. (author)

  12. Thermodynamic method for obtaining the solubilities of complex medium-sized chemicals in pure and mixed solvents

    DEFF Research Database (Denmark)

    Abildskov, Jens; O'Connell, J.P.

    2005-01-01

    This paper extends our previous simplified approach to using group contribution methods and limited data to determine differences in solubility of sparingly soluble complex chemicals as the solvent is changed. New applications include estimating temperature dependence and the effect of adding cos....... Though we present no new solution theory, the paper shows an especially efficient use of thermodynamic models for solvent and cosolvent selection for product formulations. Examples and discussion of applications are given. (c) 2004 Elsevier B.V. All rights reserved.......This paper extends our previous simplified approach to using group contribution methods and limited data to determine differences in solubility of sparingly soluble complex chemicals as the solvent is changed. New applications include estimating temperature dependence and the effect of adding...

  13. Chromium(III) Complex Obtained from Dipicolinic Acid: Synthesis, Characterization, X-Ray Crystal Structure and Electrochemical Studies

    Energy Technology Data Exchange (ETDEWEB)

    Ghasemi, Khaled; Rezvani, Ali Reza; Ghasemi, Fatemeh [Univ. of Sistan and Baluchestan, Zahedan (Iran, Islamic Republic of); Razak, Ibrahim Abdul; Rosli, Mohd Mustaqim [Universiti Sains Malaysia, Penang (Malaysia)

    2013-10-15

    The synthesis, X-ray crystallography, spectroscopic (IR, UV-vis), and electrochemical properties of the title compound, [H{sub 3}O][Cr(dipic){sub 2}] [H{sub 3}O{sup +}.Cl{sup -}] (1), (H{sub 2}dipic = 2,6-pyridinedicarboxylic acid), are reported. This complex crystallizes in the monoclinic space group Cc with a = 14.9006(10) A, b = 12.2114(8) A, c = 8.6337(6) A, α = 90.00 .deg., β = 92.7460(10) .deg., γ = 90.00 .deg., and V = 1569.16(18) A3 with Z = 4. The hydrogen bonding and noncovalent interactions play roles in the stabilization of the structure. In order to gain a better understanding of the most important geometrical parameters in the structure of the complex, atoms in molecules (AIM) method at B3LYP/6-31G level of theory has been employed.

  14. Characterization of 10 μm thick porous silicon dioxide obtained by complex oxidation process for RF application

    International Nuclear Information System (INIS)

    Park, Jeong-Yong; Lee, Jong-Hyun

    2003-01-01

    This paper proposes a 10 μm thick oxide layer structure, which can be used as a substrate for RF circuits. The structure has been fabricated by anodic reaction and complex oxidation, which is a combined process of low temperature thermal oxidation (500 deg. C, for 1 h at H 2 O/O 2 ) and a rapid thermal oxidation (RTO) process (1050 deg. C, for 1 min). The electrical characteristics of oxidized porous silicon layer (OPSL) were almost the same as those of standard thermal silicon dioxide. The leakage current through the OPSL of 10 μm was about 100-500 pA in the range of 0-50 V. The average value of breakdown field was about 3.9 MV cm -1 . From the X-ray photo-electron spectroscopy (XPS) analysis, surface and internal oxide films of OPSL, prepared by complex process were confirmed to be completely oxidized and also the role of RTO process was important for the densification of porous silicon layer (PSL) oxidized at a lower temperature. For the RF-test of Si substrate with thick silicon dioxide layer, we have fabricated high performance passive devices such as coplanar waveguide (CPW) on OPSL substrate. The insertion loss of CPW on OPSL prepared by complex oxidation process was -0.39 dB at 4 GHz and similar to that of CPW on OPSL prepared by a temperature of 1050 deg. C (1 h at H 2 O/O 2 ). Also the return loss of CPW on OPSL prepared by complex oxidation process was -23 dB at 10 GHz, which is similar to that of CPW on OPSL prepared by high temperature

  15. The treatment of irradiated uranium fuel. Results obtained while operating the pilot plant at Fontenay-aux-Roses; Le traitement de l'uranium irradie. Resultats d'exploitation de l'usine-pilote de Fontenay-aux-Roses

    Energy Technology Data Exchange (ETDEWEB)

    Regnaut, P; Faugeras, P; Brut, A; Helou, R; Redon, A [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1958-07-01

    In this paper the results obtained from four years operation of the pilot plant when using bars of increasing activity, are summarised and compared with the results of parallel studies carried out in the laboratory. As a conclusion to the article, the optimum conditions for the different phases of a process based on solvent extraction are given. (author)Fren. [French] Cette conference resume les resultats obtenus durant quatre annees de fonctionnement de l'Usine-Pilote, avec des barreaux d'activite croissante et les compare aux resultats d'etudes conduites parallelement en laboratoire. En conclusion sont donnees les conditions optima pour les differentes phases d'un procede base sur l'extraction par solvant. (auteur)

  16. Uranium extraction from Uro area phosphate ore, Nuba mountains, Sudan

    International Nuclear Information System (INIS)

    Mohammed, A. A.; Eltayeb, M. A. H.

    2003-01-01

    This study was carried out mainly to extract uranium from Uro area phosphate ore in the eastern part of Nuba mountains near Abu Gibiha town in southern Kurdufan state. For this purpose first, the phosphate ore samples were decomposed with sulphuric acid. the resulting phosphoric acid was filtered off, and pretreated with pyrite and activated charcoal. the chemical analysis of the obtained grain phosphoric acid showed that about 98% of uranium content of the phosphate ore was rendered soluble in the phosphoric acid. The clear green phosphoric acid was introduced to uranium extraction by 25% tributylphosphate (Tbp) in kerosene. The effect of several factors on the extraction and stripping processes namely, interference's effect, the suitable strip solution, the required number of extraction and stripping stages, the optimum phase ratio have been studied in details. A three stage extraction at a phase ratio (aqueous/organic) of 1:2, followed by two stages stripping using 0.5 M sodium carbonate solution at a phase ratio (A/O) of 1:4 were found to be the optimum conditions to report more than 98% of uranium content in green phosphoric acid to the aqueous phase as uranyl tricarbonate complex (UO 2 (CO 3 ) 3 ) 4- . By applying sodica decomposition upon the stripping carbonate solution using 50% sodium hydroxide, about 98% of uranium content was precipitated as sodium diuranate concentrate (Na 2 U 2 O 7 ). The chemical analysis using atomic absorption spectrometry (Aas) showed a good agreement between the specification of the obtained uranium concentrate with the standard commercial specification of sodium diuranate concentrate. Further purification was achieved for the yellow cake by selective precipitation of uranium from the solution as uranium peroxide (UO 4 .2H 2 O) using 30% hydrogen peroxide. Finally the uranium peroxide precipitated was calcined at 450 degree C to obtain the orange powder uranium trioxide (UO 3 ). The chemical analysis of the final uranium trioxide

  17. Impact of uranyl-calcium-carbonato complexes on uranium(VI) adsorption to synthetic and natural sediments.

    Science.gov (United States)

    Stewart, Brandy D; Mayes, Melanie A; Fendorf, Scott

    2010-02-01

    Adsorption on soil and sediment solids may decrease aqueous uranium concentrations and limit its propensity for migration in natural and contaminated settings. Uranium adsorption will be controlled in large part by its aqueous speciation, with a particular dependence on the presence of dissolved calcium and carbonate. Here we quantify the impact of uranyl speciation on adsorption to both goethite and sediments from the Hanford Clastic Dike and Oak Ridge Melton Branch Ridgetop formations. Hanford sediments were preconditioned with sodium acetate and acetic acid to remove carbonate grains, and Ca and carbonate were reintroduced at defined levels to provide a range of aqueous uranyl species. U(VI) adsorption is directly linked to UO(2)(2+) speciation, with the extent of retention decreasing with formation of ternary uranyl-calcium-carbonato species. Adsorption isotherms under the conditions studied are linear, and K(d) values decrease from 48 to 17 L kg(-1) for goethite, from 64 to 29 L kg (-1) for Hanford sediments, and from 95 to 51 L kg(-1) for Melton Branch sediments as the Ca concentration increases from 0 to 1 mM at pH 7. Our observations reveal that, in carbonate-bearing waters, neutral to slightly acidic pH values ( approximately 5) and limited dissolved calcium are optimal for uranium adsorption.

  18. EPR of uranium ions

    International Nuclear Information System (INIS)

    Ursu, I.; Lupei, V.

    1984-02-01

    A review of the electron paramagnetic resonance data on the uranium ions is given. After a general account of the electronic structure of the uranium free atoms and ions, the influence of the external fields (magnetic field, crystal fields) is discussed. The main information obtained from EPR studies on the uranium ions in crystals are emphasized: identification of the valence and of the ground electronic state, determination of the structure of the centers, crystal field effects, role of the intermediate coupling and of the J-mixing, role of the covalency, determination of the nuclear spin, maqnetic dipole moment and electric quadrupole moment of the odd isotopes of uranium. These data emphasize the fact that the actinide group has its own identity and this is accutely manifested at the beginning of the 5fsup(n) series encompassed by the uranium ions. (authors)

  19. Chiroptical methods in a wide wavelength range for obtaining Ln3+ complexes with circularly polarized luminescence of practical interest.

    Science.gov (United States)

    Górecki, Marcin; Carpita, Luca; Arrico, Lorenzo; Zinna, Francesco; Di Bari, Lorenzo

    2018-05-29

    We studied enantiopure chiral trivalent lanthanide (Ln3+ = La3+, Sm3+, Eu3+, Gd3+, Tm3+, and Yb3+) complexes with two fluorinated achiral tris(β-diketonate) ligands (HFA = hexafluoroacetylacetonate and TTA = 2-thenoyltrifluoroacetonate), incorporating a chiral bis(oxazolinyl)pyridine (PyBox) unit as a neutral ancillary ligand, by the combined use of optical and chiroptical methods, ranging from UV to IR both in absorption and circular dichroism (CD), and including circularly polarized luminescence (CPL). Ultimately, all the spectroscopic information is integrated into a total and a chiroptical super-spectrum, which allows one to characterize a multidimensional chemical space, spanned by the different Ln3+ ions, the acidity and steric demand of the diketone and the chirality of the PyBox ligand. In all cases, the Ln3+ ions endow the systems with peculiar chiroptical properties, either allied to f-f transitions or induced by the metal onto the ligand. In more detail, we found that Sm3+ complexes display interesting CPL features, which partly superimpose and partly integrate the more common Eu3+ properties. Especially, in the context of security tags, the pair Sm/Eu may be a winning choice for chiroptical barcoding.

  20. A Heterobimetallic Complex With an Unsupported Uranium(III)-Aluminum(I) Bond: (CpSiMe3)3U-AlCp* (Cp* = C5Me5)

    Energy Technology Data Exchange (ETDEWEB)

    Minasian, Stefan; Krinsky Ph.D., Jamin; Williams, Valerie; Arnold Ph.D., John

    2008-07-23

    The discovery of molecular metal-metal bonds has been of fundamental importance to the understanding of chemical bonding. For the actinides, examples of unsupported metal-metal bonds are relatively uncommon, consisting of Cp{sub 3}U-SnPh{sub 3}, and several actinide-transition metal complexes. Traditionally, bonding in the f-elements has been described as electrostatic; however, elucidating the degree of covalency is a subject of recent research. In carbon monoxide complexes of the trivalent uranium metallocenes, decreased {nu}{sub CO} values relative to free CO suggest that the U(III) atom acts as a {pi}-donor. Ephritikhine and coworkers have demonstrated that {pi}-accepting ligands can differentiate trivalent lanthanide and actinide ions, an effect that renders this chemistry of interest in the context of nuclear waste separation technology.

  1. Preparation and characterization of uranium-iron triple-bonded UFe(CO){sub 3}{sup -} and OUFe(CO){sub 3}{sup -} complexes

    Energy Technology Data Exchange (ETDEWEB)

    Chi, Chaoxian; Meng, Luyan; Luo, Mingbiao [School of Chemistry, Biological and Materials Sciences, State Key Laboratory Breeding Base of Nuclear Resources and Environment, East China University of Technology, Nanchang (China); Wang, Jia-Qi; Li, Wan-Lu; Li, Jun [Department of Chemistry and Key Laboratory of Organic Optoelectronics and Molecular Engineering of Ministry of Education, Tsinghua University, Beijing (China); Qu, Hui; Zhou, Mingfei [Department of Chemistry, Collaborative Innovation Center of Chemistry for Energy Materials, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Fudan University, Shanghai (China)

    2017-06-06

    We report the preparation of UFe(CO){sub 3}{sup -} and OUFe(CO){sub 3}{sup -} complexes using a laser-vaporization supersonic ion source in the gas phase. These compounds were mass-selected and characterized by infrared photodissociation spectroscopy and state-of-the-art quantum chemical studies. There are unprecedented triple bonds between U 6d/5f and Fe 3d orbitals, featuring one covalent σ bond and two Fe-to-U dative π bonds in both complexes. The uranium and iron elements are found to exist in unique formal U(I or III) and Fe(-II) oxidation states, respectively. These findings suggest that there may exist a whole family of stable df-d multiple-bonded f-element-transition-metal compounds that have not been fully recognized to date. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  2. Temperature dependent electrical characteristics of an organic-inorganic heterojunction obtained from a novel organometal Mn complex

    International Nuclear Information System (INIS)

    Ocak, Y.S.; Ebeoglu, M.A.; Topal, G.; Kilicoglu, T.

    2010-01-01

    This study includes synthesizing a Mn hexaamide (MnHA) organometal compound (C 27 H 21 N 9 O 6 MnCl 2 ).(1/2H 2 O), fabrication of MnHA/n-Si organic-inorganic heterojunction and analysis of conduction mechanism of the device over the room temperature. After synthesizing the molecule, the structure of the compound was determined using spectroscopic methods. The Sn/MnHA/n-Si structure was constructed by forming a thin MnHA layer on n-Si inorganic semiconductor and evaporating Sn metal on organic complex. The structure has shown good rectifying behavior and obeys the thermionic emission theory. The current-voltage (I-V) characteristics of the diode have been measured at temperatures ranging from 300 to 380 K at 10 K intervals to determine the temperature dependent electrical characteristics of the device.

  3. Syntheses, crystal structures and properties of novel copper(II) complexes obtained by reactions of copper(II) sulfate pentahydrate with tripodal ligands.

    Science.gov (United States)

    Zhao, Wei; Fan, Jian; Song, You; Kawaguchi, Hiroyuki; Okamura, Taka-aki; Sun, Wei-Yin; Ueyama, Norikazu

    2005-04-21

    Three novel metal-organic frameworks (MOFs), [Cu(1)SO4].H2O (4), [Cu2(2)2(SO4)2].4H2O (5) and [Cu(3)(H2O)]SO4.5.5H2O (6), were obtained by hydrothermal reactions of CuSO4.5H2O with the corresponding ligands, which have different flexibility. The structures of the synthesized complexes were determined by single-crystal X-ray diffraction analyses. Complex 4 has a 2D network structure with two types of metallacycles. Complex 5 also has a 2D network structure in which each independent 2D sheet contains two sub-layers bridged by oxygen atoms of the sulfate anions. Complex 6 has a 2D puckered structure in which the sulfate anions serve as counter anions, which are different from those in complexes 4 (terminators) and 5 (bridges). The different structures of complexes 4, 5 and 6 indicate that the nature of organic ligands affected the structures of the assemblies greatly. The magnetic behavior of complex 5 and anion-exchange properties of complex 6 were investigated.

  4. Purification of uranium metal

    International Nuclear Information System (INIS)

    Suzuki, Kenji; Shikama, Tatsuo; Ochiai, Akira.

    1993-01-01

    We developed the system for purifying uranium metal and its metallic compounds and for growing highly pure uranium compounds to study their intrinsic physical properties. Uranium metal was zone refined under low contamination conditions as far as possible. The degree of the purity of uranium metal was examined by the conventional electrical resistivity measurement and by the chemical analysis using the inductive coupled plasma emission spectrometry (ICP). The results show that some metallic impurities evaporated by the r.f. heating and other usual metallic impurities moved to the end of a rod with a molten zone. Therefore, we conclude that the zone refining technique is much effective to the removal of metallic impurities and we obtained high purified uranium metal of 99.99% up with regarding to metallic impurities. The maximum residual resistivity ratio, the r.r.r., so far obtained was about 17-20. Using the purified uranium, we are attempting to grow a highly pure uranium-titanium single crystals. (author)

  5. Regulatory impacts on the Canadian uranium industry

    International Nuclear Information System (INIS)

    Frost, S.E.

    2001-01-01

    The development of environmental and safety regulation in Canada is described and the impacts of these developments on various phases of the uranium industry are examined. In the past 25 years, seven new uranium mining projects, major expansions to four projects, and five uranium refining/conversion projects have undergone environmental assessment in Canada. As regulations and the processes for applying them have developed, the size, complexity and cost of obtaining operating approvals for uranium projects have increased exponentially. Uranium projects are subject to a level of scrutiny that goes far beyond what can be justified by their potential for environmental damage, based primarily on a perceived degree of public concern, rather than any objective measure of environmental risk. The author believes that it is time to re-examine our priorities, to establish some balance between the risks of a project and the assessment effort required. Otherwise, we shall soon find ourselves in the position where smaller projects will never be developed because they cannot cover the regulatory costs. (author)

  6. Low temperature sintering of hyperstoichiometric uranium dioxide

    International Nuclear Information System (INIS)

    Chevrel, H.

    1991-12-01

    In the lattice of uranium dioxide with hyperstoichiometric oxygen content (UO 2+x ), each additional oxygen atoms is introduced by shifting two anions from normal sites to interstitial ones, thereby creating two oxygen vacancies. The point defects then combine to form complex defects comprising several interstitials and vacancies. The group of anions (3x) in the interstitial position participate in equilibria promoting the creation of uranium vacancies thereby considerably increasing uranium self-diffusion. However, uranium grain boundaries diffusion governs densification during the first two stages of sintering of uranium dioxide with hyperstoichiometric oxygen content, i.e., up to 93% of the theoretical density. Surface diffusion and evaporation-condensation, which are considerably accentuated by the hyperstoichiometric deviation, play an active role during sintering by promoting crystalline growth during the second and third stages of sintering. U 8 O 8 can be added to adjust the stoichiometry and to form a finely porous structure and thus increase the pore area subjected to surface phenomena. The composition with an O/U ratio equal to 2.25 is found to densify the best, despite a linear growth in sintering activation energy with hyperstoichiometric oxygen content, increasing from 300 kj.mol -1 for UO 2.10 to 440 kJ.mol -1 for UO 2.25 . Seeds can be introduced to obtain original microstructures, for example the presence of large grains in small-grain matrix

  7. The uranium in the environment; L'uranium dans l'environnement

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-07-01

    The uranium is a natural element omnipresent in the environment, with a complex chemistry more and more understood. Many studies are always today devoted to this element to better improve the uranium behavior in the environment. To illustrate this knowledge and for the public information the CEA published this paper. It gathers in four chapters: historical aspects and properties of the uranium, the uranium in the environment and the impacts, the metrology of the uranium and its migration. (A.L.B.)

  8. Recovery of uranium from seawater

    International Nuclear Information System (INIS)

    Hirotsu, Takahiro; Takagi, Norio; Katoh, Shunsaku

    1995-01-01

    Present status of the development of chelating adsorbents for the recovery of uranium from seawater is outlined with emphasis on the research by the author. Uranium is estimated to exist as stable tri (carbonate) uranylate (6) ion in seawater in a very low concentration. The adsorbent for uranium from seawater in a very low concentration. The adsorbent for uranium from seawater should have high selectivity and affinity for uranium around pH 8. The required characteristics for uranium adsorbent are examined. Various chelating adsorbents have been proposed for the uranium adsorbent and their structures are discussed. Amidoxime type adsorbents have the highest adsorbing power for uranium among the adsorbents hitherto developed and fibrous amidoxime adsorbents are most promising for the practical application. Synthesis, structure and suitable shape of the amidoxime adsorbents are discussed. Uranium adsorption behavior and the amount of saturated adsorption are examined theoretically based on the complexation of an amidoxime monomer and the formula for the adsorption equiliburium is derived. The adsorption and recovery process for uranium from seawater is composed of adsorption, desorption, separation and concentration and finally, uranium is recovered as the yellow cake. A floating body mooring system is proposed by Nobukawa. (T.H.)

  9. Vacuum fusion of uranium

    International Nuclear Information System (INIS)

    Stohr, J.A.

    1957-01-01

    After having outlined that vacuum fusion and moulding of uranium and of its alloys have some technical and economic benefits (vacuum operations avoid uranium oxidation and result in some purification; precision moulding avoids machining, chip production and chemical reprocessing of these chips; direct production of the desired shape is possible by precision moulding), this report presents the uranium fusion unit (its low pressure enclosure and pumping device, the crucible-mould assembly, and the MF supply device). The author describes the different steps of cast production, and briefly comments the obtained results

  10. Preparation of uranium-230 as a new uranium tracer

    International Nuclear Information System (INIS)

    Hashimoto, T.; Kido, K.; Sotobayashi, T.

    1977-01-01

    A uranium isotope, 230 U(T=20.8 d), was produced from the 231 Pa(γ,n) 230 Pa→viaβ - decay 230 U process with a bremsstrahlung irradiation on a protactinium target. After standing for about one month to obtain a maximal growth of 230 U, the uranium was chemically purified, applying an ion-exchange method. The purity of the 230 U obtained was examined with alpha spectrometry and an intrinsic alpha peak due to 230 U as a new uranium tracer in an alpha spectrometric analysis of uranium isotopes is described. (author)

  11. Electrochemical investigation of uranium β-diketonates for all-uranium redox flow battery

    International Nuclear Information System (INIS)

    Yamamura, Tomoo; Shiokawa, Yoshinobu; Yamana, Hajimu; Moriyama, Hirotake

    2002-01-01

    The redox flow battery using uranium as the negative and the positive active materials in polar aprotic solvents was proposed. In order to establish the guiding principle for the uranium compounds as the active materials, the investigation of uranium β-diketonate complexes was conducted on (i) the solubility of active materials, (ii) the electrode reaction of U(VI) and U(IV) β-diketonate complexes and (iii) the estimation of the open circuit voltage of the battery. The solubilities of higher than 0.8 mol dm -3 of U(VI) complexes and higher than 0.4 mol dm -3 of a U(IV) complex were obtained in the solvents. The electrode reactions of U(pta) 4 , UO 2 (dpm) 2 , UO 2 (fod) 2 and UO 2 (pta) 2 were first studied and the redox potentials of uranium β-diketonates were thermodynamically discussed. The open circuit voltage is estimated more than 1 V by using Hacac or Hdpm. The larger open circuit voltage is expected when a ligand with the larger basicity is used

  12. Electrochemical investigation of tetravalent uranium β-diketones for active materials of all-uranium redox flow battery

    International Nuclear Information System (INIS)

    Yamamura, Tomoo; Shiokawa, Yoshinobu; Ikeda, Yasuhisa

    2002-01-01

    For active materials of the all-uranium redox flow battery for the power storage, tetravalent uranium β-diketones were investigated. The electrode reactions of U(ba) 4 and U(btfa) 4 were examined in comparison with that of U(acac) 4 , where ba denotes benzoylacetone, btfa benzoyltrifluoroacetone and acac acetylacetone. The cyclic voltammograms of U(ba) 4 and U(btfa) 4 solutions indicate that there are two series of redox reactions corresponding to the complexes with different coordination numbers of four and three. The electrode kinetics of the U(IV)/U(III) redox reactions for btfa complexes is examined. The obtained result supports that the uranium β-diketone complexes examined in the present study will serve as excellent active materials for negative electrolyte in the redox flow battery. (author)

  13. Paragenesis and Geochronology of the Nopal I Uranium Deposit, Mexico

    International Nuclear Information System (INIS)

    M. Fayek; M. Ren

    2007-01-01

    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

  14. Uranium(VI) sorption on iron oxides in Hanford Site sediment: Application of a surface complexation model

    International Nuclear Information System (INIS)

    Um, Wooyong; Serne, R. Jeffrey; Brown, Christopher F.; Rod, Kenton A.

    2008-01-01

    Sorption of U(VI) on Hanford fine sand (HFS) with varying Fe-oxide (especially ferrihydrite) contents showed that U(VI) sorption increased with the incremental addition of synthetic ferrihydrite into HFS, consistent with ferrihydrite being one of the most reactive U(VI) sorbents present in natural sediments. Surface complexation model (SCM) calculations for U(VI) sorption, using only U(VI) surface-reaction constants obtained from U(VI) sorption data on freshly synthesized ferrihydrite at different pHs, were similar to the measured U(VI) sorption results on pure synthetic ferrihydrite and on HFS with high contents of ferrihydrite (5 wt%) added. However, the SCM prediction using only U(VI) sorption reactions and constants for synthetic ferrihydrite overestimated U(VI) sorption on the natural HFS or HFS with addition of low amounts of added ferrihydrite (1 wt% added). Over-predicted U(VI) sorption was attributed to reduced reactivity of natural ferrihydrite present in Hanford Site sediments, compared to freshly prepared synthetic ferrihydrite. Even though the SCM general composite (GC) approach is considered to be a semi-quantitative estimation technique for contaminant sorption, which requires systematic experimental data on the sorbent-sorbate system being studied to obtain credible SCM parameters, the general composite SCM model was still found to be a useful technique for describing U(VI) sorption on natural sediments. Based on U(VI) batch sorption results, two simple U(VI) monodentate surface species, SO U O 2 HCO 3 and SO U O 2 OH on ferrihydrite and phyllosillicate in HFS, respectively, can be successfully used to describe U(VI) sorption onto Hanford Site sediment contacting varying geochemical solutions

  15. Argentinian uranium production

    International Nuclear Information System (INIS)

    Anon.

    1983-01-01

    A profit-making process for the exploitation of low grade uranium is presented. The process of lixiviation will be used, which will make it possible to obtain a final product whose humidity level will not exceed 10% and whose uranium oxide content will be no less than 68%. The operations of the plant are described. The plant can produce between 100 and 150 t of U 3 O 8 /yr in the form of yellow cake

  16. US uranium market developments

    International Nuclear Information System (INIS)

    Krusiewski, S.V.; Patterson, J.A.

    1980-01-01

    Domestic uranium delivery commitments have risen significantly since January 1979, with the bulk of deliveries scheduled after 1990. Much of the long-term procurement will be obtained from captive production. However, buyers have adjusted their delivery schedules in the near term, deferring some procurement to later years, including a portion of planned captive production. Under current commitments, US imports of foreign uranium in the 1981 to 1985 period will be greater than our exports of domestic uranium. The anticipated supply of domestic uranium through 1985 is clearly more than adequate to fill the probable US demand in the meantime, uranium producers are continuing their efforts to increase future domestic supply by their considerable investments in new or expanded mine and mill facilities. Since January 1980, average contract prices including market-price settlements, for 1980 uranium deliveries have increased slightly, but average market-price settlements made this year have decreased by several dollars. While the general trend of US uranium prices has been upward since we began reporting price data in 1973, some reductions in average prices for future deliveries appeared in 1980. The softening of prices for new procurement can be expected to be increasingly apparent in future surveys

  17. The Lagoa Real subalkaline granitic complex (south Bahia, Brazil): a source for uranium mineralizations associated with Na-Ca metasomatism

    International Nuclear Information System (INIS)

    Maruejol, P.; Cuney, M.; Poty, B.; Neto, A.M.

    1987-01-01

    In the central zone of the Sao Francisco Craton (South Bahia), the lower Proterozoic Lagoa Real granites and orthogneisses overthrust to the West the younger Urandi and Espinhaco metamorphic series, probably a late Brazilian event. This thrust is related to the regional metamorphism (amphibolite facies) of the Lagoa Real granites and induces a reverse HP metamorphism in the over thrusted series. Undeformed granites (sao Timoeto type) present two feldspars, perthitic orthoclase largely predominant over plagioclase (oligoclase ≥ albite), blue quartz, Fe-rich amphibole and biotite ± clinopyroxene assemblages, ilmenite ≥ magnetite, zircon, apatite, allanite and Nb ± Ti-REE oxides and silicates. The crystallization of the granites begins at high temperature and under low fO 2 and P H2O conditions. Fractional crystallization of pyroxene and plagioclase leads to silica enrichment during magmatic differentiation. Increasing fO 2 and P H2O are observed during this evolution. Orthogneisses show strongly recrystallized paragenesis: equal abundance of non-perthitic microcline and plagioclase (oligoclase ≤ albite), quartz, more Al-rich amphibole and biotite, magnetite, sphene, zircon, allanite, Nb ± Ti-REE oxides and silicates, and ± apatite. HT Na and Ca metasomatism occurs 330 Ma later than granite emplacement and is synchronous with important uranium mineralizations. Major elements and trace-elements geochemistry of the granites and orthogneisses indicate subalkaline to alkaline typology. Incompatible behaviour of Th, REE, Y, Zr, Nb, and F points out a convergence with alkaline magmatism. CI, F, Th, Y, REE, NB enrichments and Ba, Sr depletions are also related to a late magmatic stage. U-Th-rich and metamict accessory minerals of the granites represent a favorabl source for the Lagoa Real uranium ore-deposits [pt

  18. Uranium solubility and speciation in ground water

    International Nuclear Information System (INIS)

    Ollila, K.

    1985-04-01

    The purpose of this study has been to assess the solubility and possible species of uranium in groundwater at the disposal conditions of spent fuel. The effects of radiolysis and bentonite are considered. The assessment is based on the theoretical calculations found in the literature. The Finnish experimental results are included. The conservative estimate for uranium solubility under the oxidizing conditions caused by alpha radiolysis is based on the oxidation of uranium to the U(VI) state and formation of carbonate complex. For the groundwater with the typical carbonate content of 275 mg/l and the high carbonate content of 485 mg/l due to bentonite, the solubility values of 360 mg u/l and 950 mg U/l, are obtained, respectively. The experimental results predict considerably lower values, 0.5-20 mg U/l. The solubility of uranium under the undisturbed reducing conditions may be calculated based on the hydrolysis, carbonate complexation and redox reactions. The results vary considerably depending on the thermodynamic data used. The wide ranges of the most important groundwater parameters are seen in the solubility values. The experimental results show the same trends. As a conservative value for the solubility in reducing groundwater 50-500 μg U/l is estimated. (author)

  19. Physicochemical aspects of extraction of uranium concentrate from the wastes and thermodynamic characteristics of thorium-uranium compounds

    International Nuclear Information System (INIS)

    Khamidov, F.A.

    2017-01-01

    The purpose of present work is elaboration of physicochemical aspects of extraction of uranium concentrate from the wastes and study of thermodynamic characteristics of thorium-uranium compounds. Therefore, the radiological monitoring of tailing dumps of Tajikistan has been conducted; the obtaining of uranium concentrate from the tailing dumps of uranium production has been studied; the obtaining of uranium concentrate from the tailing dumps of uranium production with application of local sorbents has been studied as well; thermal stability and thermodynamic characteristics of uranium-thorium compounds has been investigated; the flowsheets of extraction of uranium concentrate from the wastes have been elaborated.

  20. Uranium exploration techniques in Bolivia

    International Nuclear Information System (INIS)

    Virreira, V.

    1981-01-01

    The exploration techniques used by the Bolivian Nuclear Energy Commission/Comision Boliviana de Energia Nuclear (COBOEN) in certain areas of Bolivia that are considered promising from the standpoint of uranium deposits are presented in summary form. The methods and results obtained are described, including the techniques used by the Italian company AGIP-URANIUM during four years of exploration under contract with COBOEN. Statistical data are also given explaining the present level of uranium exploration in Bolivia. (author)

  1. Inherently safe in situ uranium recovery

    Science.gov (United States)

    Krumhansl, James L; Brady, Patrick V

    2014-04-29

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

  2. Uranium recovery from mine water

    International Nuclear Information System (INIS)

    Sarkar, K.M.

    1984-01-01

    In many plant trials it has been proven that very small amounts (10 to 20 ppm) of uranium dissolved in mine water can be effectively recovered by the use of ion exchange resins and this uranium recovery has many advantages. In this paper an economic analysis at different levels of uranium contamination and at different market prices of uranium are described. For this study an operating mine-mill complex with a sulphuric acid leach circuit, followed by solvent extraction (SX) process, is considered, where contaminated mine water is available in excess of process requirements. It is further assumed that the sulphuric acid eluant containing uranium would be mixed with the mill pregnant liquor stream that proceeds to the SX plant for final uranium recovery

  3. Uranium dioxide pellets

    International Nuclear Information System (INIS)

    Zawidzki, T.W.

    1982-01-01

    A process for the preparation of a sintered, high density, large crystal grain size uranium dioxide pellet is described which involves: (i) reacting a uranyl nitrate of formula UO 2 (NO 3 ) 2 .6H 2 O with a sulphur source, at a temperature of from about 300 deg. C to provide a sulphur-containing uranium trioxide; (ii) reacting the thus-obtained modified uranium trioxide with ammonium nitrate to form an insoluble sulphur-containing ammonium uranate; (iii) neutralizing the thus-formed slurry with ammonium hydroxide to precipitate out as an insoluble ammonium uranate the remaining dissolved uranium; (iv) recovering the thus-formed precipitates in a dry state; (v) reducing the dry precipitate to UO 2 , and forming it into 'green' pellets; and (vi) sintering the pellets in a hydrogen atmosphere at an elevated temperature

  4. Czechoslovak uranium

    International Nuclear Information System (INIS)

    Pluskal, O.

    1992-01-01

    Data and knowledge related to the prospecting, mining, processing and export of uranium ores in Czechoslovakia are presented. In the years between 1945 and January 1, 1991, 98,461.1 t of uranium were extracted. In the period 1965-1990 the uranium industry was subsidized from the state budget to a total of 38.5 billion CSK. The subsidies were put into extraction, investments and geologic prospecting; the latter was at first, ie. till 1960 financed by the former USSR, later on the two parties shared costs on a 1:1 basis. Since 1981 the prospecting has been entirely financed from the Czechoslovak state budget. On Czechoslovak territory uranium has been extracted from deposits which may be classified as vein-type deposits, deposits in uranium-bearing sandstones and deposits connected with weathering processes. The future of mining, however, is almost exclusively being connected with deposits in uranium-bearing sandstones. A brief description and characteristic is given of all uranium deposits on Czechoslovak territory, and the organization of uranium mining in Czechoslovakia is described as is the approach used in the world to evaluate uranium deposits; uranium prices and actual resources are also given. (Z.S.) 3 figs

  5. Peroxo complexes of molybdenum(VI), tungsten(VI), uranium(VI), zirconium(IV) and thorium(IV) ions containing tridentate Schiff bases derived from salicylaldehyde and amino acids

    International Nuclear Information System (INIS)

    Tarafder, M.T.H.; Khan, A.R.

    1997-01-01

    The synthesis of peroxo complexes of molybdenum(VI), tungsten(VI), uranium(VI), zirconium(IV), thorium(IV) and their possible oxygen transfer reactions is presented. An attempt has also been made to study the size of the metal ions and the electronic effect derived from the tridentate Schiff bases on the v 1 (O-O) mode of the complexes in their IR spectra

  6. Oxygen isotope fractionation in uranium oxides

    International Nuclear Information System (INIS)

    Zheng Yongfei

    1995-01-01

    Thermodynamic oxygen isotope factors for uranium oxides have been calculated by means of the modified increment method. The sequence of 18 O-enrichment in the uranium oxides with respect to the common rock-forming minerals is predicted as follows: spinel 3 < illite. Two sets of self-consistent fractionation factors between the uranium oxides and water and between the uranium oxides and the other minerals have been obtained for 0∼1200 degree C. The theoretical results are applicable to the isotopic geothermometry of uranium ores when pairing with other gangue minerals in hydrothermal uranium deposits

  7. Spectrophotometric determination of uranium with arsenazo previous liquid-liquid extraction and colour development in organic medium

    International Nuclear Information System (INIS)

    Palomares Delgado, F.; Vera Palomino, J.; Petrement Eguiluz, J. C.

    1964-01-01

    The determination of uranium with arsenazo is hindered by a great number of cation which form stable complexes with the reactive and may given rise to serious interferences. By studying the optimum conditions of uranium the extraction be means of tributylphosphate solutions dissolved in methylisobuthylketone, under conditions for previous masking of the interfering cations, an organic extract was obtained containing all the uranium together with small amounts of iron. The possible interference derived from the latter element is avoided by reduction with hydroxylammoniumchlorid followed by complex formation of the Fe(II)-ortophenantroline compound in alcoholic medium. (Author) 17 refs

  8. Uranium(VI) sorption onto magnetite. Increasing confidence in surface complexation models using chemically evident surface chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Bok, Frank [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Surface Processes

    2017-06-01

    Surface complexation models have made great efforts in describing the sorption of various radionuclides on naturally occurring mineral phases. Unfortunately, many of the published sorption parameter sets are built upon unrealistic or even wrong surface chemistry. This work describes the benefit of combining spectroscopic and batch sorption experimental data to create a reliable and consistent surface complexation parameter set.

  9. Uranium removal from organic solutions of PUREX process

    International Nuclear Information System (INIS)

    Dell'Occhio, L.A.; Dupetit, G.A.; Pascale, A.A.; Vicens, H.E.

    1987-01-01

    During the uranium extraction process with tributyl phosphate (TBP) in nitric medium, a bi solvated, non hydrated complex is formed, of formula UO2(NO3)2TBP, which is soluble in the diluent, a paraffin hydrocarbon. As it is known that some uranium salts, for instance the nitrate, when dissolved in organic solvents, like isopropanol, can be discharged as complex molecules at the cathode of an electrodeposition cell, it was decided to apply this technique to uranium loaded TBP solutions. From preliminary experiments resulted a practical possibility for the analytical control through the alpha measurement of electro deposits. This technique could be applied as well to the treatment of depleted organic streams carrying undesirable alpha activity, because the so treated solutions become deprived of uranium. This work presents the curves obtained working at constant voltage with uranium-loaded TBP solutions, the determination of the optimal operation voltage in these conditions, the electrodeposition yield for electro polished copper and stainless steel cathodes and the tests of reproducibility of deposits. A summary of the results obtained operating the high voltage supply at constant power is also presented. (Author)

  10. Direct extraction of uranium and plutonium from oxide fuel using TBP-HNO3 complex for super-DIREX process

    International Nuclear Information System (INIS)

    Miura, S.; Kamiya, M.; Nomura, K.; Koyama, T.; Ogum, S.; Shimada, T.; Mori, Y.; Enokida, Y.

    2004-01-01

    Super-DIREX is a new reprocessing method which has high economical efficiency. Experimental study of this process was started on the direct extraction of U and Pu from irradiated MOX fuel by the supercritical carbon dioxide (SFCO 2 ) containing TBP-HNO 3 complex. This report describes direct extraction of U and Pu with TBP-HNO 3 complex at atmospheric pressure, as the first test for irradiated fuel, in order to investigate the applicability of SFCO 2 containing TBP-HNO 3 complex. In this test, dependency on dissolution temperature, Pu content, fuel/ TBP-HNO 3 complex ratio and effect of voloxidation were investigated. From these results, TBP-HNO 3 complex was found to be effective in the respect of the recovery of U and Pu. The number of the process step in dissolution and co-extraction is small, and amount of waste can be reduced. It is applicable to the direct extraction in Super-DIREX. (authors)

  11. Relationship of the vibrational frequency of the uranyl ion with the uranium electronegativity

    International Nuclear Information System (INIS)

    Rodriguez S, A.; Martinez Q, E.

    1990-07-01

    It has been demonstrated that the vibrational asymmetric frequency of the uranyl ion, it experiences a consistent spectrochemical displacement with the variations of electronegativity of the uranium in their complexes. The values of the electronegativity of the uranium they were dear by means of calculations that it involves measures of those lengths of the connection uranium-oxygen, obtained by vibrational spectroscopy, effective nuclear charges and the Allred and Rochow equation. The results show the evidence of a natural order that relates to the vibrational frequency with the electronegativity of the uranium atom; settling down that if the electronegativity is graph against it bond length to the oxygen or to it frequency value, a simple relationship is obtained as a form to obtain clear responses in absence of complementary information. (Author)

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

    International Nuclear Information System (INIS)

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

    1995-11-01

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

  13. X-ray spectroscopic studies of microbial transformations of uranium

    International Nuclear Information System (INIS)

    Dodge, C.J.; Francis, A.J.; Clayton, C.R.

    1995-10-01

    Several uranium compounds U-metal (α-phase), UO 2 , U 3 O 8 , γ-UO 3 , uranyl acetate, uranyl nitrate, uranyl sulfate, aqueous and solid forms of 1:1 U:citric acid and 1:1:2 U:Fe:citric acid mixed-metal complexes, and a precipitate obtained by photodegradation of the U-citrate complex were characterized by X-ray spectroscopy using XPS, XANES, and EXAFS. XPS and XANES were used to determine U oxidation states. Spectral shifts were obtained at the U 4f 7/2 and U 4f 5/2 binding energies using XPS, and at the uranium M V absorption edge using XANES. The magnitude of the energy shift with oxidation state, and the ability to detect mixed-valent forms make these ideal techniques for determining uranium speciation in wastes subjected to bacterial action. The structure of 1:1 U:citric acid complex in both the aqueous and solid state was determined by EXAFS analysis of hexavalent uranium at the L M absorption edge and suggests the presence of a binuclear complex with a (UO 2 ) 2 (μ,η 2 -citrato) 2 core with a U-U distance of 5.2 angstrom. The influence of Fe on the structure of U-citrate complex was determined by EXAFS and the presence of a binuclear mixed-metal citrate complex with a U-Fe distance of 4.8 angstrom was confirmed. The precipitate resulting from photodegradation of U-citrate complex was identified as an amorphous form of uranium trioxide by XPS and EXAS

  14. Multinuclear NMR spectroscopy of the tetrahedral uranium(IV) complex U(BH3CH3)4

    International Nuclear Information System (INIS)

    Gamp, E.; Shinomoto, R.; Edelstein, N.; McGarvey, B.R.

    1987-01-01

    The temperature dependence of the 1 H, 11 B, and 13 C NMR spectra of T/sub d/ U(BH 3 CH 3 ) 4 in solution is reported. The paramagnetic shifts are interpreted as originating purely from spin delocalization mechanisms with no contribution from the metal-orbital dipolar interaction. It is shown that the temperature dependence of both 1 H shifts (bridging and terminal protons) is identical with that calculated from a polarization theory which assumes the shift is proportional to the average value of electron spin in the inner 5f orbitals. The proportionality constant is -5.64 MHz for the bridging protons and -0.59 MHz for the terminal protons. The temperature dependences of 11 B and 13 shifts are found to depart significantly from that predicted by the polarization theory with the largest deviations shown by the 11 B shifts. It is shown how those deviations can be accounted for by postulating a second spin delocalization through direct covalency involving molecular orbitals formed from the uranium 5f orbitals and ligand s and p orbitals. 29 references, 4 figures, 3 tables

  15. Highly dispersive ion exchangers in the analytical chemistry of uranium, particularly regarding separation methods

    International Nuclear Information System (INIS)

    Schoening, R.

    1975-01-01

    The reaction of water-insoluble polyvinyl pyrrolidon with uranium VI was investigated and a determination method for uranium was worked out in which the polyvinyl pyrrolidon was used as specific exchanger. Good separations of uranium from numerous transition metal ions were achieved here. The application of this exchanger for a fast and simple elution and determination method was of particular importance. A possible sorption mechanism was suggested based on the capacity curve of uranium with polyvinyl pyrrolidon and nitrogen and chloride content at maximum load. The sorption occurs by coordination of the carbonyl oxygen of single pyrrolidon rings with the protons of the complex acides and uranium. This assumption is supported by IR investigations. The sorbability of other inorganic acids was also investigated and possible structures were formulated for the sorption mechanism. In addition to this, ion exchangers were prepared based on cellulose by converting cellulose powder with aziridine and tris-1-aziridinyl-phosphine oxide. A polyethylene imine cellulose of high capacity was obtained in the conversion of cellulose powder with aziridine. This exchanger absorbs cobalt III very strongly. The exchanger loaded with cobalt III was used to separate the uranium as cyanato complex. The exchanger obtained in converting chlorated cellulose with tris-1-aziridinyl phosphine oxide also absorbs uranium VI very strongly. Thus a separation method of high specifity and selectivity was developed. (orig.) [de

  16. World uranium resources

    International Nuclear Information System (INIS)

    Deffeyes, K.S.; MacGregor, I.D.

    1980-01-01

    To estimate the total resource availability of uranium, the authors' approach has been to ask whether the distribution of uranium in the earth's crust can be reasonably approximated by a bell-shaped log-normal curve. In addition they have asked whether the uranium deposits actually mined appear to be a portion of the high-grade tail, or ascending slope, of the distribution. This approach preserves what they feel are the two most important guiding principles of Hubbert's work, for petroleum, namely recognizing the geological framework that contains the deposits of interest and examining the industry's historical record of discovering those deposits. Their findings, published recently in the form of a book-length report prepared for the US Department of Energy, suggest that for uranium the crustal-distribution model and the mining-history model can be brought together in a consistent picture. In brief, they conclude that both sets of data can be described by a single log-normal curve, the smoothly ascending slope of which indicates approximately a 300-fold increase in the amount of uranium recoverable for each tenfold decrease in ore grade. This conclusion has important implications for the future availability of uranium. They hasten to add, however, that this is only an approximative argument; no rigorous statistical basis exists for expecting a log-normal distribution. They continue, pointing out the enormously complex range of geochemical behavior of uranium - and its wide variety of different binds of economic deposit. Their case study, supported by US mining records, indicates that the supply of uranium will not be a limiting factor in the development of nuclear power

  17. Recovery of uranium from lignites

    International Nuclear Information System (INIS)

    Hurst, F.J.

    1980-01-01

    Uranium in raw lignite is associated with the organic matter and is readily soluble in acid (and carbonate) solutions. However, beneficiation techniques were not successful for concentrating the uranium or removing part of the reagent-consuming materials. Once the lignite was heated, the uranium became much less soluble in both acid and carbonate solutions, and complete removal of carbon was required to convert it back to a soluble form. Proper burning improves acid-leaching efficiency; that is, it reduces the reagent consumption and concentrates the uranium, thereby reducing plant size for comparable uranium throughput, and it eliminates organic fouling of leach liquors. Restrictions are necessary during burning to prevent the uranium from becoming refractory. The most encouraging results were obtained by flash-burning lignite at 1200 to 1300 0 C and utilizing the released SO 2 to supplement the acid requirement. The major acid consumers were aluminum and iron

  18. Uranium ores

    International Nuclear Information System (INIS)

    Poty, B.; Roux, J.

    1998-01-01

    The processing of uranium ores for uranium extraction and concentration is not much different than the processing of other metallic ores. However, thanks to its radioactive property, the prospecting of uranium ores can be performed using geophysical methods. Surface and sub-surface detection methods are a combination of radioactive measurement methods (radium, radon etc..) and classical mining and petroleum prospecting methods. Worldwide uranium prospecting has been more or less active during the last 50 years, but the rise of raw material and energy prices between 1970 and 1980 has incited several countries to develop their nuclear industry in order to diversify their resources and improve their energy independence. The result is a considerable increase of nuclear fuels demand between 1980 and 1990. This paper describes successively: the uranium prospecting methods (direct, indirect and methodology), the uranium deposits (economical definition, uranium ores, and deposits), the exploitation of uranium ores (use of radioactivity, radioprotection, effluents), the worldwide uranium resources (definition of the different categories and present day state of worldwide resources). (J.S.)

  19. Uranium market

    International Nuclear Information System (INIS)

    Rubini, L.A.; Asem, M.A.D.

    1990-01-01

    The historical development of the uranium market is present in two periods: The initial period 1947-1970 and from 1970 onwards, with the establishment of a commercial market. The world uranium requirements are derived from the corresponding forecast of nuclear generating capacity, with, particular emphasis to the brazilian requirements. The forecast of uranium production until the year 2000 is presented considering existing inventories and the already committed demand. The balance between production and requirements is analysed. Finally the types of contracts currently being used and the development of uranium prices in the world market are considered. (author)

  20. Uranium enrichment

    International Nuclear Information System (INIS)

    1990-01-01

    This report looks at the following issues: How much Soviet uranium ore and enriched uranium are imported into the United States and what is the extent to which utilities flag swap to disguise these purchases? What are the U.S.S.R.'s enriched uranium trading practices? To what extent are utilities required to return used fuel to the Soviet Union as part of the enriched uranium sales agreement? Why have U.S. utilities ended their contracts to buy enrichment services from DOE?

  1. Contribution to uranium geochemistry in intrusive granites; Contribution a la geochimie de l'uranium dans les granites intrusifs

    Energy Technology Data Exchange (ETDEWEB)

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

    1959-01-15

    This work aims to define the position of a certain number of French granitic deposits within the field of the geochemistry of granites in general, and of the geochemistry of uranium in particular. The regions concerned are: - 3 French Hercynian ranges, in the Vendee, in Brittany and in the Morvan, - 1 African range, probably precambrian, of the Hoggar. For each range, the petrochemical framework is first of all determined and then the degree of chemical homogeneity of the rocks is evaluated. In the petrochemical groups thus obtained the geochemical behaviour of the uranium is studied. From a point of view of the geochemistry of the granites under investigation, a comparison of the laws of distribution of the major elements in the 4 ranges shows up a convergence of average composition which was not anticipated by geological and petrographic considerations alone. The statistical and geochemical distribution laws of the total uranium as a function of the petrochemical variations are established. A study of the chemical forms of uranium in the rocks has drawn an attention to the qualitative and quantitative importance of the fraction of this uranium soluble in dilute acids. We have therefore reconsidered on the one hand, the laws of distribution of the insoluble uranium, which represents essentially the uranium fixed in crystalline structures (zircon, allanite...), and we have justified on the other hand the interest presented by the soluble uranium: this, although more complex in character, presents a geochemical unity in post magmatic phenomena which makes possible to find a genetic connection between the uraniferous deposits and the intrusive massifs. Finally we have given a plan of the geochemical cycle of uranium, in which we hope to have provided some more accurate data on the igneous phase. (author) [French] Le but du travail presente est de situer sur le plan de la geochimie des granites en general, sur le plan de la geochimie de l'uranium en particulier, un

  2. Contribution to uranium geochemistry in intrusive granites; Contribution a la geochimie de l'uranium dans les granites intrusifs

    Energy Technology Data Exchange (ETDEWEB)

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

    1959-01-15

    This work aims to define the position of a certain number of French granitic deposits within the field of the geochemistry of granites in general, and of the geochemistry of uranium in particular. The regions concerned are: - 3 French Hercynian ranges, in the Vendee, in Brittany and in the Morvan, - 1 African range, probably precambrian, of the Hoggar. For each range, the petrochemical framework is first of all determined and then the degree of chemical homogeneity of the rocks is evaluated. In the petrochemical groups thus obtained the geochemical behaviour of the uranium is studied. From a point of view of the geochemistry of the granites under investigation, a comparison of the laws of distribution of the major elements in the 4 ranges shows up a convergence of average composition which was not anticipated by geological and petrographic considerations alone. The statistical and geochemical distribution laws of the total uranium as a function of the petrochemical variations are established. A study of the chemical forms of uranium in the rocks has drawn an attention to the qualitative and quantitative importance of the fraction of this uranium soluble in dilute acids. We have therefore reconsidered on the one hand, the laws of distribution of the insoluble uranium, which represents essentially the uranium fixed in crystalline structures (zircon, allanite...), and we have justified on the other hand the interest presented by the soluble uranium: this, although more complex in character, presents a geochemical unity in post magmatic phenomena which makes possible to find a genetic connection between the uraniferous deposits and the intrusive massifs. Finally we have given a plan of the geochemical cycle of uranium, in which we hope to have provided some more accurate data on the igneous phase. (author) [French] Le but du travail presente est de situer sur le plan de la geochimie des granites en general, sur le plan de la geochimie de l'uranium en particulier

  3. Can we predict uranium bioavailability based on soil parameters? Part 2: soil solution uranium concentration is not a good bioavailability index.

    Science.gov (United States)

    Vandenhove, H; Van Hees, M; Wannijn, J; Wouters, K; Wang, L

    2007-01-01

    The present study aimed to quantify the influence of soil parameters on uranium uptake by ryegrass. Ryegrass was established on eighteen distinct soils, spiked with (238)U. Uranium soil-to-plant transfer factors (TF) ranged from 0.0003 to 0.0340kgkg(-1). There was no significant relation between the U soil-to-plant transfer (or total U uptake or flux) and the uranium concentration in the soil solution or any other soil factor measured, nor with the U recovered following selective soil extractions. Multiple linear regression analysis resulted in a significant though complex model explaining up to 99% of variation in TF. The influence of uranium speciation on uranium uptake observed was featured: UO(2)(+2), uranyl carbonate complexes and UO(2)PO(4)(-) seem the U species being preferentially taken up by the roots and transferred to the shoots. Improved correlations were obtained when relating the uranium TF with the summed soil solution concentrations of mentioned uranium species.

  4. Filtration aids in uranium ore processing

    International Nuclear Information System (INIS)

    Ford, H.L.; Levine, N.M.; Risdon, A.R.

    1975-01-01

    A process of improving the filtration efficiency and separation of uranium ore pulps obtained by carbonate leaching of uranium ore which comprises treating said ore pulps with an aqueous solution of hydroxyalkyl guar selected from the group consisting of hydroxyethyl and hydroxypropyl guar in the amount of 0.1 and 2.0 pounds of hydroxyalkyl guar per ton of uranium ore

  5. Rare-earth- and uranium-mesoionic carbenes. A new class of f-block carbene complex derived from an N-heterocyclic olefin

    Energy Technology Data Exchange (ETDEWEB)

    Seed, John A.; Gregson, Matthew; Chilton, Nicholas F.; Wooles, Ashley J.; Liddle, Stephen T. [School of Chemistry, The University of Manchester (United Kingdom); Tuna, Floriana; McInnes, Eric J.L. [School of Chemistry and Photon Science Institute, The University of Manchester (United Kingdom)

    2017-09-11

    Neutral mesoionic carbenes (MICs) have emerged as an important class of carbene, however they are found in the free form or ligated to only a few d-block ions. Unprecedented f-block MIC complexes [M(N''){sub 3}{CN(Me)C(Me)N(Me)CH}] (M=U, Y, La, Nd; N''=N(SiMe{sub 3}){sub 2}) are reported. These complexes were prepared by a formal 1,4-proton migration reaction when the metal triamides [M(N''){sub 3}] were treated with the N-heterocyclic olefin H{sub 2}C=C(NMeCH){sub 2}, which constitutes a new, general way to prepare MIC complexes. Quantum chemical calculations on the 5f{sup 3} uranium(III) complex suggest the presence of a U=C donor-acceptor bond, composed of a MIC→U σ-component and a U(5f)→MIC(2p) π-back-bond, but for the d{sup 0}f{sup 0} Y and La and 4f{sup 3} Nd congeners only MIC→M σ-bonding is found. Considering the generally negligible π-acidity of MICs, this is surprising and highlights that greater consideration should possibly be given to recognizing MICs as potential π-acid ligands when coordinated to strongly reducing metals. (copyright 2017 The Authors. Published by Wiley-VCH Verlag GmbH and Co. KGaA.)

  6. Meeting of the French geological society - Uranium: geology, geophysics, chemistry. Book of abstracts; Reunion de la Societe Geologique de France - Uranium: geologie, geophysique, chimie. Recueil des resumes

    Energy Technology Data Exchange (ETDEWEB)

    Zakari, A.A.; Mima, S.; Bidaud, A.; Criqui, P.; Menanteau, P.; David, S.; Pagel, M.; Chagnes, A.; Cote, G.; Courtaud, B.; Thiry, J.; Miehe, J.M.; Gilbert, F.; Cuney, M.; Bruneton, P.; Ewington, D.; Vautrin-Ul, C.; Cannizzo, C.; Betelu, S.; Chausse, A.; Ly, J.; Bourgeois, D.; Maynadie, J.; Meyer, D.; Clavier, N.; Costin, D.T.; Cretaz, F.; Szenknect, S.; Ravaux, J.; Poinssot, C.; Dacheux, N.; Durupt, N.; Blanvillain, J.J.; Geffroy, F.; Aparicio, B.; Dubessy, J.; Nguyen-Trung, C.; Robert, P.; Uri, F.; Beaufort, D.; Lescuyer, J.L.; Morichon, E.; Allard, T.; Milesi, J.P.; Richard, A.; Rozsypal, C.; Mercadier, J.; Banks, D.A.; Boiron, M.C.; Cathelineau, M.; Dardel, J.; Billon, S.; Patrier, P.; Wattinne, A.; Vanderhaeghe, O.; Fabre, C.; Castillo, M.; Salvi, S.; Beziat, D.; Williams-Jones, A.E.; Trap, P.; Durand, C.; Goncalves, P.; Marquer, D.; Feybesse, J.L.; Richard, Y.; Orberger, B.; Hofmann, A.; Megneng, M.; Orberger, B.; Bouttemy, M.; Vigneron, J.; Etcheberry, A.; Perdicakis, M.; Prignon, N.; Toe, W.; Andre-Mayer, A.S.; Eglinger, A.; Jordaan, T.; Hocquet, S.; Ledru, P.; Selezneva, V.; Vendryes, G.; Lach, P.; Cuney, M.; Mercadier, J.; Brouand, M.; Duran, C.; Seydoux-Guillaume, A.M.; Bingen, B.; Parseval, P. de; Guillaume, D.; Bosse, V.; Paquette, J.L.; Ingrin, J.; Montel, J.M.; Giot, R.; Maucotel, F.; Hubert, S.; Gautheron, C.; Tassan-Got, L.; Pagel, M.; Barbarand, J.; Cuney, M.; Lach, P.; Bonhoure, J.; Leisen, M.; Kister, P.; Salaun, A.; Villemant, B.; Gerard, M.; Komorowski, J.C.; Michel, A.; Riegler, T.; Tartese, R.; Boulvais, P.; Poujols, M.; Gloaguen, E.; Mazzanti, M.; Mougel, V.; Nocton, G.; Biswas, B.; Pecaut, J.; Othmane, G.; Menguy, N.; Vercouter, T.; Morin, G.; Galoisy, L.; Calas, G.; Fayek, M.

    2010-11-15

    -temperature, and metallogenic provinces; 21 - Magmatic-hydrothermal transition in the Roessing pegmatite: implications for uranium mineralisation; 22 - Deformation and partial fusion of a Archean-paleo-Proterozoic crust: implication on uraniferous ores mobilization and deposition, Torngats orogenesis, Ungava bay; 23 - Black chert pebbles of the Pongola basin conglomerates ({approx}2, 9 Ga - South Africa): a potential uranium source?; 24 - origin and evolution of detrital pyrites in meso-Archean conglomerates (3.08-2.64 Ga) of South Africa: uranium source or trap?; 25 - Experimental study of U(VI) carbonates with respect to 3 parameters: pH, carbonate concentration, temperature, using vibrational (Raman, FTIR, ATR) and optical (UV-visible) spectroscopy; 26 - Nature and significance of the contact between the Abbabis gneiss complex and the meta-sedimentary sequences of the Damara orogenic belt; 27 - Metallogenic potentialities of Proterozoic orogenic belts accreted to Archean basements: the Damara/Lufilien orogen - Namibia and Zambia; 28 - Contribution of the Geological Exploration to the development of the KATCO ISR mine - Chu-Sarysu basin, Kazakhstan; 29 - Remarks about some remarkable events which occurred during the Francevillien formation; 30 - Geochemical signature of different mineral phases obtained by ICP-MS laser ablation (trace elements and rare earths): Application Uranium deposits; 31 - Role of fluids and irradiation in complex pegmatite euxenite/zircon assemblies from Norway and their U-Pb geochronological consequences; 32 - Mechanical modeling of rupture around metamictic minerals; 33 - Helium diffusion in apatite: Effect alpha recoil-linked damages; 34 - Rare earth spectra in uranium oxides: a marker of the uranium deposit type; 35 - Rare earths: tracers of uranium behaviour during acid sulphated hydrothermal weathering - the Guadeloupe example; 36 - What metallogenic model for the Kiggavik-Andrew Lake trend? Nunavut, Canada; 37 - Uranium mobility in the Southern

  7. Uranium mining during the Cold War. The Wismut plant in the Soviet atomic complex; Uranbergbau im Kalten Krieg. Die Wismut im sowjetischen Atomkomplex. Bd. 1. Studien

    Energy Technology Data Exchange (ETDEWEB)

    Boch, Rudolf [TU Chemnitz (Germany). Wirtschafts- und Sozialgeschichte; Karlsch, Rainer (ed.)

    2011-07-01

    The book on the Wismut plant covers the following issues: Introduction: history of uranium mining of Wismut. Significance of uranium mining in politics and science: Uranium for the strategic equilibrium; the ore of the Cold War; special zones; ''Party within the Party'', radiation protection in uranium mining; Freiberg's geoscientists searching strategic metals in the 1940ies; end of the shift. Social history and daily routine: Good money for hard work; foreign among ''friends''; personnel data; gainful employment for women and emancipation in the frame of mining; from symphony orchestra to laymen circles; the fightning spirit of pitman-sportsmen.

  8. Automated uranium titration system

    International Nuclear Information System (INIS)

    Takahashi, M.; Kato, Y.

    1983-01-01

    An automated titration system based on the Davies-Gray method has been developed for accurate determination of uranium. The system consists of a potentiometric titrator with precise burettes, a sample changer, an electronic balance and a desk-top computer with a printer. Fifty-five titration vessels are loaded in the sample changer. The first three contain the standard solution for standardizing potassium dichromate titrant, and the next two and the last two contain the control samples for data quality assurance. The other forty-eight measurements are carried out for sixteen unknown samples. Sample solution containing about 100 mg uranium is taken in a titration vessel. At the pretreatment position, uranium (VI) is reduced to uranium (IV) by iron (II). After the valency adjustment, the vessel is transferred to the titration position. The rate of titrant addition is automatically controlled to be slower near the end-point. The last figure (0.01 mL) of the equivalent titrant volume for uranium is calculated from the potential change. The results obtained with this system on 100 mg uranium gave a precision of 0.2% (RSD,n=3) and an accuracy of better than 0.1%. Fifty-five titrations are accomplished in 10 hours. (author)

  9. A comparative study of the complexation of uranium(VI) with oxydiacetic acid and its amide derivatives

    International Nuclear Information System (INIS)

    Rao, Linfeng; Tian, Guoxin

    2005-01-01

    There has been significant interest in recent years in the studies of alkyl-substituted amides as extractants for actinide separation because the products of radiolytic and hydrolytic degradation of amides are less detrimental to separation processes than those of organophosphorus compounds traditionally used in actinide separations. Stripping of actinides from the amide-containing organic solvents is relatively easy. In addition, the amide ligands are completely incinerable so that the amount of secondary wastes generated in nuclear waste treatment could be significantly reduced. One group of alkyl-substituted oxa-diamides have been shown to be promising in the separation of actinides from nuclear wastes. For example, tetraoctyl-3-oxa-glutaramide and tetraisobutyl-oxa-glutaramide form actinide complexes that can be effectively extracted from nitric acid solutions. To understand the thermodynamic principles governing the complexation of actinides with oxa-diamides, we have studied the complexation of U(VI) with dimethyl-3-oxa-glutaramic acid (DMOGA) and tetramethyl-3-oxa-glutaramide (TMOGA) in aqueous solutions, in comparison with oxydiacetic acid (ODA) (Figure 1). Previous studies have indicated that the complexation of U(VI) with ODA is strong and entropy-driven. Comparing the results for DMOGA and TMOGA with those for ODA could provide insight into the energetics of amide complexation with U(VI) and the relationship between the thermodynamic properties and the ligand structure

  10. Laser based analytical spectroscopy of uranium

    International Nuclear Information System (INIS)

    Argekar, A.A.; Kulkarni, M.J.; Godbole, S.V.; Page, A.G.; Samuel, J.K.; Paranjape, D.B.; Singh Mudher, K.D.

    1992-01-01

    Analytical spectroscopy of uranium has been studied using a XeCl excimer laser, using the fluorescence emission of U(VI) ions doped in a solid solution of sodium fluoride (NaF) and sodium chloride (NaCl) in 3:2 proportion. An electronic circuitry involving time-gating of the photomultiplier tube and facility to integrate the analytical signal over ten laser pulses has been developed to enable laser operation and signal detection with high S/N ratio. The matrix enhanced U(VI) fluorescence emission is free from chemical and spectral interferences due to the concomitant presence of ten metallic elements generally associated with uranium. The digital signal output is highly precise and does not saturate upto 5 ppm uranium concentration. X-ray diffraction patterns obtained for uranium doped compounds at 2.5% and 10% dopant concentrations are broadly similar to that of Na 2 U 2 O 7 . The detailed studies have, however, revealed fine structure for individual peaks, thereby, revealing the formation of sodium fluoro-uranate complex which is responsible for the enhanced intensity of fluorescence emission. (author). 10 refs., 6 figs., 2 tabs

  11. Uranium enrichment

    International Nuclear Information System (INIS)

    1989-01-01

    GAO was asked to address several questions concerning a number of proposed uranium enrichment bills introduced during the 100th Congress. The bill would have restructured the Department of Energy's uranium enrichment program as a government corporation to allow it to compete more effectively in the domestic and international markets. Some of GAO's findings discussed are: uranium market experts believe and existing market models show that the proposed DOE purchase of a $750 million of uranium from domestic producers may not significantly increase production because of large producer-held inventories; excess uranium enrichment production capacity exists throughout the world; therefore, foreign producers are expected to compete heavily in the United States throughout the 1990s as utilities' contracts with DOE expire; and according to a 1988 agreement between DOE's Offices of Nuclear Energy and Defense Programs, enrichment decommissioning costs, estimated to total $3.6 billion for planning purposes, will be shared by the commercial enrichment program and the government

  12. Uranium resources

    International Nuclear Information System (INIS)

    1976-01-01

    This is a press release issued by the OECD on 9th March 1976. It is stated that the steep increases in demand for uranium foreseen in and beyond the 1980's, with doubling times of the order of six to seven years, will inevitably create formidable problems for the industry. Further substantial efforts will be needed in prospecting for new uranium reserves. Information is given in tabular or graphical form on the following: reasonably assured resources, country by country; uranium production capacities, country by country; world nuclear power growth; world annual uranium requirements; world annual separative requirements; world annual light water reactor fuel reprocessing requirements; distribution of reactor types (LWR, SGHWR, AGR, HWR, HJR, GG, FBR); and world fuel cycle capital requirements. The information is based on the latest report on Uranium Resources Production and Demand, jointly issued by the OECD's Nuclear Energy Agency (NEA) and the International Atomic Energy Agency. (U.K.)

  13. A high-throughput 2D-analytical technique to obtain single protein parameters from complex cell lysates for in silico process development of ion exchange chromatography.

    Science.gov (United States)

    Kröner, Frieder; Elsäßer, Dennis; Hubbuch, Jürgen

    2013-11-29

    The accelerating growth of the market for biopharmaceutical proteins, the market entry of biosimilars and the growing interest in new, more complex molecules constantly pose new challenges for bioseparation process development. In the presented work we demonstrate the application of a multidimensional, analytical separation approach to obtain the relevant physicochemical parameters of single proteins in a complex mixture for in silico chromatographic process development. A complete cell lysate containing a low titre target protein was first fractionated by multiple linear salt gradient anion exchange chromatography (AEC) with varying gradient length. The collected fractions were subsequently analysed by high-throughput capillary gel electrophoresis (HT-CGE) after being desalted and concentrated. From the obtained data of the 2D-separation the retention-volumes and the concentration of the single proteins were determined. The retention-volumes of the single proteins were used to calculate the related steric-mass action model parameters. In a final evaluation experiment the received parameters were successfully applied to predict the retention behaviour of the single proteins in salt gradient AEC. Copyright © 2013 Elsevier B.V. All rights reserved.

  14. Coordination chemistry of actinide elements: preparation of new uranium complexes with schiff bases and their characterization (Preprint No. CT-31)

    International Nuclear Information System (INIS)

    Hingorani, S.; Reddy, P.S.N.; Agarwala, B.V.

    1988-02-01

    The Schiff bases, o-vanillin semicarbazone (oVSC) and 2-pyridine carboxaldehyde isonicotinoyl hydrazone (PCINH) have been prepared and their novel complexes with dioxouranium(VI) have been synthesized and characterized by IR spectra, elemental analysis and other physico-chemical techniques. (author)

  15. The influence of a selenium-chromium-lipid complex obtained from Chlorella vulgaris on the energy metabolism in rats with experimental diabetes

    Directory of Open Access Journals (Sweden)

    O. Y. Lukashiv

    2017-07-01

    Full Text Available One of the leading roles in treating diabetes mellitus belongs to chrome ions therapy (III, especially in the complex with selenium (IV. Currently selenium is obtained from unicellular algae, which contain biologically active substances and which are capable of accumulating exogenous microelements. By incubating unicellular algae Chlorella vulgaris Biej. in the conditions of aquaculture with sodium selenite (IV and chromium (III chloride, we obtained a biologically active lipid substance which contains selenium and chromium. The substance was tested for the impact on energy metabolism of animals exposed to experimentally induced diabetes mellitus. The diabetes was caused by modeling obesity of the animals with further injection of streptozotocin in the amount of 65 mg/kg and nicotinamide at the dose of 230 mg/kg. The rats were intragastrically injected with 1 ml of 1% starch solution which contained a selenium-chrome-lipid complex extracted from the Chlorella containing 0.6 µg of selenium, 1.05 µg of chrome and 0.5 mg of lipids for prophylactic, therapeutic and prophylactic-therapeutic purposes; the other group of rats for therapeutic purposes was injected with starch solution with the same composition of microelements in inorganic form – sodium selenite (IV and chromium chloride (III. This paper presents the results of our study of the impact of organic and inorganic compounds of chrome and selenium on the energetic metabolism of rats exposed to experimental diabetes mellitus. The analysis determined that in the rats’ organism, the selenium-chrome-lipid complex from the Chlorella improved the indicators of the energetic metabolism – in the group of rats which received it for therapeutic purposes, we observed an up to 7.5 fold increase in the activity of succinate dehydrogenase compared to the rats which did not receive therapeutic treatment. The increase in the activity of succinate dehydrogenase corresponded to the increase in the

  16. Influence of Ambient Gas on Laser-Induced Breakdown Spectroscopy of Uranium Metal

    International Nuclear Information System (INIS)

    Zhang Dacheng; Ma Xinwen; Wang Shulong; Zhu Xiaolong

    2015-01-01

    Laser-induced breakdown spectroscopy (LIBS) is regarded as a suitable method for the remote analysis of materials in any phase, even in an environment with high radiation levels. In the present work we used the third harmonic pulse of a Nd:YAG laser for ablation of uranium metal and measured the plasma emission with a fiber-optic spectrometer. The LIBS spectra of uranium metal and their features in different ambient gases (i.e., argon, neon, oxygen, and nitrogen) at atmospheric pressure were studied. Strong continuum spectrum and several hundreds of emission lines from UI and UII were observed. It is found that the continuum spectrum observed in uranium not only comes from bremsstrahlung emission but is also due to the complex spectrum of uranium. The influence of ambient gas and the gas flow rate for ablation of uranium metal was investigated. The experimental results indicate that the intensity of the uranium lines was enhanced in argon and nitrogen. However, the intensity of uranium lines was decreased in oxygen due to the generation of UO and other oxides. The results also showed that the highest intensity of uranium lines were obtained in argon gas with a gas flow rate above 2.5 L/min. The enhanced mechanism in ambient gas and the influence of the gas flow rate were analyzed in this work. (paper)

  17. Removing and recovering of uranium from the acid mine waters by using ion exchange resin

    International Nuclear Information System (INIS)

    Nascimento, Marcos Roberto Lopes do

    1998-01-01

    Ion exchange using resins is one of the few processes capable of reducing ionic contaminants in effluents to very low levels. In this study the process was used to remove and recovery uranium from acid mine waters at Pocos de Caldas-MG Uranium Mining and Milling Plant. The local mineralogical features, allied to the biogeochemical phenomena, owing to presence of pyrite in the rock piles, moreover another factors, resulting acid drainage with several pollutants, including uranium ranging from 6 to 14 mg/l, as sulfate complex, that can be removed by anionic exchanger. The iron interference is eliminated by lime pretreatment of water, increasing pH from 2.6 to 3.3-3.8 to precipitate this cation, without changing the uranium amount. Eight anionic resins were tested, based on the uranium loading, in sorption studies. Retention time, and pH influence was verified for the exchanger chose. With breakthrough of 1 mg U/L and 10 mg U/l in the feed solution, the uranium decontamination level was 94%. Typical values of loading resin were 20-30 g U/l and 70-90 g SO 4 /l. Uranium elution was done with Na Cl solution. Retention time, saline, and acid concentration were the parameters studied. The concentrate, obtained from the eluate by ammonia precipitation, presented uranium (86,8% as U 3 O 8 ) and impurities within commercial specifications. (author)

  18. Larger red-shift in optical emissions obtained from the thin films of globular proteins (BSA, lysozyme) – polyelectrolyte (PAA) complexes

    Energy Technology Data Exchange (ETDEWEB)

    Talukdar, Hrishikesh [Physical Sciences Division, Institute of Advanced Study in Science and Technology, Vigyan Path, Paschim Boragaon, Garchuk, Guwahati 781035, Assam (India); Kundu, Sarathi, E-mail: sarathi.kundu@gmail.com [Physical Sciences Division, Institute of Advanced Study in Science and Technology, Vigyan Path, Paschim Boragaon, Garchuk, Guwahati 781035, Assam (India); Basu, Saibal [Solid State Physics Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India)

    2016-09-30

    Graphical abstract: Thin films of protein-polyelectrolyte complexes show larger red-shift in optical emission. - Highlights: • Globular proteins (lysozyme and BSA) and polyelectrolyte (sodium polyacrylic acid) are used to form protein-polyelectrolyte complexes (PPC). • Larger red-shift in optical emission is obtained from the thin films of PPC. • Red-shift is not obtained from the solution of PPC and pure protein thin films. • Larger red-shift from PPC films is due to the energy dissipation as non-radiative form through interactions with nearby atoms. • Red-shift in optical emission is independent on the thickness of the PPC film. - Abstract: Globular proteins (lysozyme and BSA) and polyelectrolyte (sodium polyacrylic acid) are used to form protein-polyelectrolyte complexes (PPC). Out-of-plane structures of ≈30–60 nm thick PPC films and their surface morphologies have been studied by using X-ray reflectivity and atomic force microscopy, whereas optical behaviors of PPC and protein conformations have been studied by using UV–vis, photoluminescence and FTIR spectroscopy respectively. Our study reveals that thin films of PPC show a larger red-shift of 23 and 16 nm in the optical emissions in comparison to that of pure protein whereas bulk PPC show a small blue-shift of ≈3 nm. A small amount of peak-shift is found to occur due to the heat treatment or concentration variation of the polyelectrolyte/protein in bulk solution but cannot produce such film thickness independent larger red-shift. Position of the emission peak remains nearly unchanged with the film thickness. Mechanism for such larger red-shift has been proposed.

  19. Complex formation in the system uranium(VI) - alpha-substituted carboxylic acids studied by TRLFS. Pt. III. Alpha-aminoisobutyric acid at pH 4

    International Nuclear Information System (INIS)

    Moll, H.; Geipel, G.; Bernhard, G.; Fanghaenel, Th.; Grenthe, I.

    2002-01-01

    At higher ligand concentrations a 1:2 complex between UO 2 2+ and α-aminoisobutyric acid was observed at pH 4. Fluorescence lifetimes and spectra were obtained for UO 2 [NH 3 C(CH 3 ) 2 COO] 2 2+ . The complex formation constant was found to be log β 1:2 = 2.07±0.25. (orig.)

  20. Uranium supply and demand

    Energy Technology Data Exchange (ETDEWEB)

    Spriggs, M J

    1976-01-01

    Papers were presented on the pattern of uranium production in South Africa; Australian uranium--will it ever become available; North American uranium resources, policies, prospects, and pricing; economic and political environment of the uranium mining industry; alternative sources of uranium supply; whither North American demand for uranium; and uranium demand and security of supply--a consumer's point of view. (LK)

  1. Diffusive gradient in thin FILMS (DGT) compared with soil solution and labile uranium fraction for predicting uranium bioavailability to ryegrass.

    Science.gov (United States)

    Duquène, L; Vandenhove, H; Tack, F; Van Hees, M; Wannijn, J

    2010-02-01

    The usefulness of uranium concentration in soil solution or recovered by selective extraction as unequivocal bioavailability indices for uranium uptake by plants is still unclear. The aim of the present study was to test if the uranium concentration measured by the diffusive gradient in thin films (DGT) technique is a relevant substitute for plant uranium availability in comparison to uranium concentration in the soil solution or uranium recovered by ammonium acetate. Ryegrass (Lolium perenne L. var. Melvina) is grown in greenhouse on a range of uranium spiked soils. The DGT-recovered uranium concentration (C(DGT)) was correlated with uranium concentration in the soil solution or with uranium recovered by ammonium acetate extraction. Plant uptake was better predicted by the summed soil solution concentrations of UO(2)(2+), uranyl carbonate complexes and UO(2)PO(4)(-). The DGT technique did not provide significant advantages over conventional methods to predict uranium uptake by plants. Copyright 2009 Elsevier Ltd. All rights reserved.

  2. Diffusive gradient in thin FILMS (DGT) compared with soil solution and labile uranium fraction for predicting uranium bioavailability to ryegrass

    Energy Technology Data Exchange (ETDEWEB)

    Duquene, L. [SCK-CEN, Biosphere Impact Studies, Boeretang 200, B-2400 Mol (Belgium); Vandenhove, H., E-mail: hvandenh@sckcen.b [SCK-CEN, Biosphere Impact Studies, Boeretang 200, B-2400 Mol (Belgium); Tack, F. [Ghent University, Laboratory for Analytical Chemistry and Applied Ecochemistry, Coupure Links 653, B-9000 Gent (Belgium); Van Hees, M.; Wannijn, J. [SCK-CEN, Biosphere Impact Studies, Boeretang 200, B-2400 Mol (Belgium)

    2010-02-15

    The usefulness of uranium concentration in soil solution or recovered by selective extraction as unequivocal bioavailability indices for uranium uptake by plants is still unclear. The aim of the present study was to test if the uranium concentration measured by the diffusive gradient in thin films (DGT) technique is a relevant substitute for plant uranium availability in comparison to uranium concentration in the soil solution or uranium recovered by ammonium acetate. Ryegrass (Lolium perenne L. var. Melvina) is grown in greenhouse on a range of uranium spiked soils. The DGT-recovered uranium concentration (C{sub DGT}) was correlated with uranium concentration in the soil solution or with uranium recovered by ammonium acetate extraction. Plant uptake was better predicted by the summed soil solution concentrations of UO{sub 2}{sup 2+}, uranyl carbonate complexes and UO{sub 2}PO{sub 4}{sup -}. The DGT technique did not provide significant advantages over conventional methods to predict uranium uptake by plants.

  3. Diffusive gradient in thin FILMS (DGT) compared with soil solution and labile uranium fraction for predicting uranium bioavailability to ryegrass

    International Nuclear Information System (INIS)

    Duquene, L.; Vandenhove, H.; Tack, F.; Van Hees, M.; Wannijn, J.

    2010-01-01

    The usefulness of uranium concentration in soil solution or recovered by selective extraction as unequivocal bioavailability indices for uranium uptake by plants is still unclear. The aim of the present study was to test if the uranium concentration measured by the diffusive gradient in thin films (DGT) technique is a relevant substitute for plant uranium availability in comparison to uranium concentration in the soil solution or uranium recovered by ammonium acetate. Ryegrass (Lolium perenne L. var. Melvina) is grown in greenhouse on a range of uranium spiked soils. The DGT-recovered uranium concentration (C DGT ) was correlated with uranium concentration in the soil solution or with uranium recovered by ammonium acetate extraction. Plant uptake was better predicted by the summed soil solution concentrations of UO 2 2+ , uranyl carbonate complexes and UO 2 PO 4 - . The DGT technique did not provide significant advantages over conventional methods to predict uranium uptake by plants.

  4. Anticorrosion protection of uranium

    Energy Technology Data Exchange (ETDEWEB)

    Goncharov, Ivan D.; Kazakovskaya, Tatiana; Tukmakov, Victor; Shapovalov, Vyacheslav [Russian Federal Nuclear Center-VNIIEF, 37, Mira Ave., RU-607190 Sarov (Nizhnii Gorod), 010450 (Russian Federation)

    2004-07-01

    Uranium in atmospheric conditions is non-stable. Sloughing products are being generated on its surface during storage or use. These corrosion products make many difficulties because of necessity to provide personnel safety. Besides, uranium corrosion may cause damage in parts. The first works devoted to uranium corrosion were performed in the framework of the USA Manhattan Project in the early forties of last century. Various methods of uranium protection were investigated, among them the galvanic one was the most studied. Later on the galvanic technology was patented. The works on this problem remains urgent up to the present time. In Russia, many methods of uranium corrosion protection, mainly against atmospheric corrosion, were tried on. In particular, such methods as diffusion zinc and paint coating were investigated. In the first case, a complex intermetallic U-Zn compound was formed but its protection was not reliable enough, this protection system was inconvenient and uncertain and that is why an additional paint coating was necessary. In the case of paint coatings another problem appeared. It was necessary to find such a coating where gas-permeability would prevail over water-permeability. Otherwise significant uranium corrosion occurs. This circumstance together with low mechanical resistance of paint coatings does not allow to use paint coating for long-term protection of uranium. Currently, there are following methods of uranium protection: ion-plasma, galvanic and thermo-vacuum annealing. These are described in this paper. In the end the issue of corrosion protection in reactor core zones is addressed. Here the greatest difficulties are caused when enriched uranium heated up to 500 deg. C needs anticorrosion protection. In this case various metal coatings are not reliable because of brittle inter-metallide formation. The reliable protection may be provided only up to the temperature plus 400 - 500 deg. C with the help of galvanic copper coating since

  5. Anticorrosion protection of uranium

    International Nuclear Information System (INIS)

    Goncharov, Ivan D.; Kazakovskaya, Tatiana; Tukmakov, Victor; Shapovalov, Vyacheslav

    2004-01-01

    Uranium in atmospheric conditions is non-stable. Sloughing products are being generated on its surface during storage or use. These corrosion products make many difficulties because of necessity to provide personnel safety. Besides, uranium corrosion may cause damage in parts. The first works devoted to uranium corrosion were performed in the framework of the USA Manhattan Project in the early forties of last century. Various methods of uranium protection were investigated, among them the galvanic one was the most studied. Later on the galvanic technology was patented. The works on this problem remains urgent up to the present time. In Russia, many methods of uranium corrosion protection, mainly against atmospheric corrosion, were tried on. In particular, such methods as diffusion zinc and paint coating were investigated. In the first case, a complex intermetallic U-Zn compound was formed but its protection was not reliable enough, this protection system was inconvenient and uncertain and that is why an additional paint coating was necessary. In the case of paint coatings another problem appeared. It was necessary to find such a coating where gas-permeability would prevail over water-permeability. Otherwise significant uranium corrosion occurs. This circumstance together with low mechanical resistance of paint coatings does not allow to use paint coating for long-term protection of uranium. Currently, there are following methods of uranium protection: ion-plasma, galvanic and thermo-vacuum annealing. These are described in this paper. In the end the issue of corrosion protection in reactor core zones is addressed. Here the greatest difficulties are caused when enriched uranium heated up to 500 deg. C needs anticorrosion protection. In this case various metal coatings are not reliable because of brittle inter-metallide formation. The reliable protection may be provided only up to the temperature plus 400 - 500 deg. C with the help of galvanic copper coating since

  6. The blue complexes of U in aqueous solutions

    International Nuclear Information System (INIS)

    Musikas, C.

    1976-01-01

    Mixed-valence uranium complexes were synthesized. Hydrolysis of hexavalent U leads to anionic species soluble in aqueous solutions when the UO 2 ++ ions are neutralized by tetraalkylammonium hydroxides. These complexes are polynuclear and the size and interatomic distances found for the polyanions are those of macromolecules. By hydrazine of these complexes, solutions were obtained and their absorption spectra studied. The spectra of U(VI) and U(V) ions are observed, together with new bands attributable to a charge transfer. It may be concluded that the blue complexes of uranium are type II composite-valence complexes for which the delocalization coefficient α can be calculated [fr

  7. Anti-infective properties of the melanin-glucan complex obtained from medicinal tinder bracket mushroom, Fomes fomentarius (L.: Fr.) Fr. (Aphyllophoromycetideae).

    Science.gov (United States)

    Seniuk, Olga F; Gorovoj, Leontiy F; Beketova, Galina V; Savichuk, Hatalia O; Rytik, Petr G; Kucherov, Igor I; Prilutskay, Alla B; Prilutsky, Alexandr I

    2011-01-01

    The goal of this investigation was to comparatively study the efficiency of traditionally used anti-infective drugs and biopolymer complexes originated from the medicinal mushroom Fomes fomentarius (L.:Fr.) Fr.: 1) water-soluble melanin-glucan complex (MGC; -80% melanins and -20% beta-glucans) and 2) insoluble chitin-glucan-melanin complex (ChGMC; -70% chitin, -20% beta-glucans, and -10% melanins). Infectious materials (Helicobacter pylori, Candida albicans, and Herpes vulgaris I and HIV-1(zmb) were used in pure cultures of in vitro and in vivo models on experimental animals. Comparison studies of fungal biopolymers and effective modern antifungal, antibacterial, and antiviral drugs were used in in vitro models. The comparative clinical efficiency of ChGMC and of etiotropic pharmaceuticals in models of H. pylori, C. albicans, and H. vulgaris I infection contamination were studied. Using in vitro models, it was established that MGC completely depresses growth of C. albicans. MGC had an antimicrobial effect on H. pylori identical to erythromycin in all concentrations, and had a stronger action on this bacterium than other tested antibiotics. Tested MGC possesses simultaneously weak toxicity and high anti-HIV-1 activity in comparison with zidovudine (Retrovir). The obtained results show that CLUDDT therapy in Wistar rats with the application of ChGMC is, on average, 1.35-1.43 times as effective as a traditional one. Considering the absence of MGC and ChGMC toxic properties on blood cells even in very high concentrations, these complexes may be used as a source of biopolymers for the creation of essentially new agents for wide application in infectious pathology.

  8. On medicative application of complexons in the case of uranium intoxication

    International Nuclear Information System (INIS)

    Ivannikov, A.T.

    1987-01-01

    The report deals with the problem of accelerating the uranium elimination from the body in the light of present knowledge. Based on data available in the literature and obtained by the author, effects of sodium bicarbonate, complexons (polyamine-polycarbonic acids) and their phosphonic analogues - polyamine-polyalkyl-phosphonic acids (AMPAs) in the case of uranium intoxication have been analysed. Thus, sodium bicarbonate recommended by the ICRP and IAEA as a remedy for uranium intoxication produces some adverse action reducing its efficiency, while warning against complexons because of risk for kidneys proved to be unjustified. Experimental evidence presented demonstrates conclusively that AMPAs are the most efficient complexing agents for uranium binding and eliminating from the body, essentially superior to complexons due to greater stability constants of AMPA with uranyl ion. AMPAs form stable protonated complexes with uranyl ion which are resistant to acid medium typical of certain kidney parts, so that decomposition of these complexes and deposition of uranium are prevented, thus lowering risk for kidneys. This compares favourably with sodium bicarbonate whose complex with uranyl ion is rather unstable at low pH values. An AMPA compound, Na 6 Ca 2 -diethylene-triamine-pentamethyl- phosphonic acid (the preparation called trimephacin), is adopted in the USSR as an antidote for uranium intoxication and proposed to be included into ICRP Recommendations. (author)

  9. 77 FR 51579 - Application for a License To Export High-Enriched Uranium

    Science.gov (United States)

    2012-08-24

    ... NUCLEAR REGULATORY COMMISSION Application for a License To Export High-Enriched Uranium Pursuant.... Complex, July 30, 2012, August Uranium (93.35%). uranium-235 high-enriched 1, 2012, XSNM3726, 11006037. contained in 7.5 uranium in the kilograms uranium. form of broken metal to the Atomic Energy of Canada...

  10. New french uranium mineral species; Nouvelles especes uraniferes francaises

    Energy Technology Data Exchange (ETDEWEB)

    Branche, G; Chervet, J; Guillemin, C [Commissariat a l' Energie Atomique, Lab. du Fort de Chatillon, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1952-07-01

    In this work, the authors study the french new uranium minerals: parsonsite and renardite, hydrated phosphates of lead and uranium; kasolite: silicate hydrated of uranium and lead uranopilite: sulphate of uranium hydrated; bayleyite: carbonate of uranium and of hydrated magnesium; {beta} uranolite: silicate of uranium and of calcium hydrated. For all these minerals, the authors give the crystallographic, optic characters, and the quantitative chemical analyses. On the other hand, the following species, very rare in the french lodgings, didn't permit to do quantitative analyses. These are: the lanthinite: hydrated uranate oxide; the {alpha} uranotile: silicate of uranium and of calcium hydrated; the bassetite: uranium phosphate and of hydrated iron; the hosphuranylite: hydrated uranium phosphate; the becquerelite: hydrated uranium oxide; the curite: oxide of uranium and lead hydrated. Finally, the authors present at the end of this survey a primary mineral: the brannerite, complex of uranium titanate. (author) [French] Dans ce travail, les auteurs etudient les nouveaux mineraux uraniferes francais: parsonsite et renardite, phosphates hydrates de plomb et d'uranium; kasolite: silicate hydrate d'uranium et de plomb uranopilite: sulfate d'uranium hydrate; bayleyite: carbonate d'uranium et de magnesium hydrate; {beta} uranolite: silicate d'uranium et de calcium hydrate. Pour tous ces mineraux, les auteurs donnent les caracteres cristallographiques, optiques, et les analyses chimiques quantitatives. Par contre, les especes suivantes, tres rares dans les gites francais, n'ont pas permis d'effectuer d'analyses quantitatives. Ce sont: l'ianthinite: oxyde uraneux hydrate; l'{alpha} uranotile: silicate d'uranium et de calcium hydrate; le bassetite: phosphate d'uranium et de fer hydrate; la hosphuranylite: phosphate duranium hydrate; la becquerelite: oxyde d'uranium hydrate; la curite: oxyde d'uranium et de plomb hydrate. Enfin, les auteurs presentent a la fin de cette etude

  11. Uranium exploration and mining in Australia

    International Nuclear Information System (INIS)

    Wutzler, B.

    1984-01-01

    Uranium minerals were discovered in Australia in the years 1850 to 1900 already, but most of them were not recognised as such. It was not until 1894 that the first significant uranium find was made in Carcoar, west of Sydney. At that time, the uranium output of the world, which only amounted to a few hundred cwts, was for the most part obtained from mining areas close to the border between Saxony and Bohemia. In South Australia, uranium ore was mined experimentally for the production of radium at Radium Hill from 1906 onwards and at Mt. Painter from 1910 onwards. It was not until World War II, however, that uranium gained importance as a valuable raw material that could also be used for military purposes. The second phase of uranium mining in Australia commenced in 1944. Within ten years Australia's presumed uranium potential was confirmed by extensive exploration. The development of uranium mining in Australia is described in the present paper. (orig.)

  12. Adsorption of Rh(III) complexes from chloride solutions obtained by leaching chlorinated spent automotive catalysts on ion-exchange resin Diaion WA21J

    International Nuclear Information System (INIS)

    Shen Shaobo; Pan Tonglin; Liu Xinqiang; Yuan Lei; Wang Jinchao; Zhang Yongjian; Guo Zhanchen

    2010-01-01

    It was found that Rh, Pd and Pt contained in the spent ceramic automotive catalysts could be effectively extracted by dry chlorination with chlorine. In order to concentrate Rh(III) ions contained in the chloride solutions obtained, thermodynamic and kinetics studies for adsorption of Rh(III) complexes from the chloride solutions on an anionic exchange resin Diaion WA21J were carried out. Rh, Pd, Pt, Al, Fe, Si, Zn and Pb from the chloride solution could be adsorbed on the resin. The distribution coefficients (K d ) of Rh(III) decreased with the increase in initial Rh(III) concentration or in adsorption temperature. The isothermal adsorption of Rh(III) was found to fit Langmuir, Freundlich and Dubinin-Kaganer-Radushkevich models under the adsorption conditions. The maximum monolayer adsorption capacities Q max based on Langmuir adsorption isotherms were 6.39, 6.61 and 5.81 mg/g for temperatures 18, 28 and 40 deg. C, respectively. The apparent adsorption energy of Rh was about -7.6 kJ/mol and thus Rh(III) adsorption was a physical type. The experimental data obtained could be better simulated by pseudo-first-order kinetic model and the activation energy obtained was 6.54 J/mol. The adsorption rate of Rh(III) was controlled by intraparticle diffusion in most of time of adsorption process.

  13. Chemical aspects of the precise and accurate determination of uranium and plutonium from nuclear fuel solutions

    International Nuclear Information System (INIS)

    Heinonen, O.J.

    1981-01-01

    A method for the simultaneous or separate determination of uranium and plutonium has been developed. The method is based on the sorption of uranium and plutonium as their chloro complexes on Dowex 1x10 column. When separate uranium and plutonium fractions are desired, plutonium ions are reduced to Pu (III) and eluted, after which the uranium ions are eluted with dilute HCl. Simultaneous stripping of a mass ratio U/Pu approximately 1 fraction for mass spectrometric measurements is achieved by proper choice of eluant HC1 concentration. Special attention was paid to the obtaining of americium free plutonium fractions. The distribution coefficient measurements showed that at 12.5-M HCl at least 30 % of americium ions formed anionic chloro complexes. The chemical aspects of isotopic fractionation in a multiple filament thermal ionization source were also investigated. Samples of uranium were loaded as nitrates, chlorides, and sulphates and the dependence of the measured uranium isotopic ratios on the chemical form of the loading solution as well as on the filament material was studied. Likewise the dependence of the formation of uranium and its oxide ions on various chemical and instrumental conditions was investigated using tungsten and rhenium filaments. Systematic errors arising from the chemical conditions are compared with errors arising from the automatic evaluation of of spectra. (author)

  14. Extractive separation of uranium(VI) as perchlorate/chloroacetate complexes with 1-phenyl-2,3 dimethyl-5-pyrazolone and its applications

    International Nuclear Information System (INIS)

    Bose, R.; Murty, D.S.R.

    2003-01-01

    The extraction of U(VI) with 1-phenyl 2,3 dimethyl-5-pyrazolone, at a pH of 2.5, in the presence of common anions, like perchlorate and tri-, di-, and monochloroacetates has been investigated. The optimum experimental conditions have been evaluated by studying various parameters such as pH, equilibration period, reagent concentration, metal concentration, and solvents. Effect of diverse anions and cations on the extraction has also been studied. The extracted species, determined by log D - log R plots are represented as, [UO 2 (Apy) 4 (ClO 4 ) 2 ], [UO 2 (Apy) 2 (TCA) 2 ], [UO 2 (Apy) 2 (DCA) 2 ], [UO 2 (Apy)(H 2 O)(MCA) 2 ]. The conditional stability constants of the quantitatively extracted complexes are calculated. The proposed method allows the selective separation of uranium(VI) from multicomponent mixtures and geological matrices and is also applied for the separation and chemical characterization of impurities at trace and ultratrace levels. (author)

  15. Contribution to the study of gaseous Carburization of Uranium; Contribucion al estudio de la Carburacion gaesosa del uranio

    Energy Technology Data Exchange (ETDEWEB)

    Esteban Hernandez, J A; Jimenez Moreno, J M; Villota Ruiz, P de

    1966-07-01

    Thermal decomposition of uranium hydride powder obtained by hydrogenation of uranium turnings is studied on the first part of this paper. Carburization of the uranium hydride or metallic uranium powder with methane is studied in the second part. A method of uranium monocarbide fabrication under static atmosphere is described. On this method hydrogen is removed by means of an uranium getter. (Author) 6 refs.

  16. Alkaline lixiviation of uranium in granitic pegmatite

    International Nuclear Information System (INIS)

    Jambor, S.

    1980-06-01

    The work described herein concerns the determination of the experimental optimum conditions for the alkaline lixiviation of uranium based on the following parameters: time, pH, temperature, density and grane size. The samples were obtained from the Supamo complex, near the Currupia river in the Piar District of the Bolivar State in Venezuela. They have a granitic composition and graphitic texture. The uranium was found in them as a secondary oxidized mineral of green-yellow colour localized in fractures fissures, intergranular spaces and also in the mica as. Secondary uranitite. The lixiviation process was carried out using Na 2 CO 3 /NaHCO 3 buffer solution and for 100 gr. samples the best values for an efficient process were found by using 170 mesh grane size and 500 ml of pH buffer at 70 0 C for a 24 hour time period. (author)

  17. Meeting of the French geological society - Uranium: geology, geophysics, chemistry. Book of abstracts

    International Nuclear Information System (INIS)

    Zakari, A.A.; Mima, S.; Bidaud, A.; Criqui, P.; Menanteau, P.; David, S.; Pagel, M.; Chagnes, A.; Cote, G.; Courtaud, B.; Thiry, J.; Miehe, J.M.; Gilbert, F.; Cuney, M.; Bruneton, P.; Ewington, D.; Vautrin-Ul, C.; Cannizzo, C.; Betelu, S.; Chausse, A.; Ly, J.; Bourgeois, D.; Maynadie, J.; Meyer, D.; Clavier, N.; Costin, D.T.; Cretaz, F.; Szenknect, S.; Ravaux, J.; Poinssot, C.; Dacheux, N.; Durupt, N.; Blanvillain, J.J.; Geffroy, F.; Aparicio, B.; Dubessy, J.; Nguyen-Trung, C.; Robert, P.; Uri, F.; Beaufort, D.; Lescuyer, J.L.; Morichon, E.; Allard, T.; Milesi, J.P.; Richard, A.; Rozsypal, C.; Mercadier, J.; Banks, D.A.; Boiron, M.C.; Cathelineau, M.; Dardel, J.; Billon, S.; Patrier, P.; Wattinne, A.; Vanderhaeghe, O.; Fabre, C.; Castillo, M.; Salvi, S.; Beziat, D.; Williams-Jones, A.E.; Trap, P.; Durand, C.; Goncalves, P.; Marquer, D.; Feybesse, J.L.; Richard, Y.; Orberger, B.; Hofmann, A.; Megneng, M.; Orberger, B.; Bouttemy, M.; Vigneron, J.; Etcheberry, A.; Perdicakis, M.; Prignon, N.; Toe, W.; Andre-Mayer, A.S.; Eglinger, A.; Jordaan, T.; Hocquet, S.; Ledru, P.; Selezneva, V.; Vendryes, G.; Lach, P.; Cuney, M.; Mercadier, J.; Brouand, M.; Duran, C.; Seydoux-Guillaume, A.M.; Bingen, B.; Parseval, P. de; Guillaume, D.; Bosse, V.; Paquette, J.L.; Ingrin, J.; Montel, J.M.; Giot, R.; Maucotel, F.; Hubert, S.; Gautheron, C.; Tassan-Got, L.; Pagel, M.; Barbarand, J.; Cuney, M.; Lach, P.; Bonhoure, J.; Leisen, M.; Kister, P.; Salaun, A.; Villemant, B.; Gerard, M.; Komorowski, J.C.; Michel, A.; Riegler, T.; Tartese, R.; Boulvais, P.; Poujols, M.; Gloaguen, E.; Mazzanti, M.; Mougel, V.; Nocton, G.; Biswas, B.; Pecaut, J.; Othmane, G.; Menguy, N.; Vercouter, T.; Morin, G.; Galoisy, L.; Calas, G.; Fayek, M.

    2010-11-01

    -temperature, and metallogenic provinces; 21 - Magmatic-hydrothermal transition in the Roessing pegmatite: implications for uranium mineralisation; 22 - Deformation and partial fusion of a Archean-paleo-Proterozoic crust: implication on uraniferous ores mobilization and deposition, Torngats orogenesis, Ungava bay; 23 - Black chert pebbles of the Pongola basin conglomerates (∼2, 9 Ga - South Africa): a potential uranium source?; 24 - origin and evolution of detrital pyrites in meso-Archean conglomerates (3.08-2.64 Ga) of South Africa: uranium source or trap?; 25 - Experimental study of U(VI) carbonates with respect to 3 parameters: pH, carbonate concentration, temperature, using vibrational (Raman, FTIR, ATR) and optical (UV-visible) spectroscopy; 26 - Nature and significance of the contact between the Abbabis gneiss complex and the meta-sedimentary sequences of the Damara orogenic belt; 27 - Metallogenic potentialities of Proterozoic orogenic belts accreted to Archean basements: the Damara/Lufilien orogen - Namibia and Zambia; 28 - Contribution of the Geological Exploration to the development of the KATCO ISR mine - Chu-Sarysu basin, Kazakhstan; 29 - Remarks about some remarkable events which occurred during the Francevillien formation; 30 - Geochemical signature of different mineral phases obtained by ICP-MS laser ablation (trace elements and rare earths): Application Uranium deposits; 31 - Role of fluids and irradiation in complex pegmatite euxenite/zircon assemblies from Norway and their U-Pb geochronological consequences; 32 - Mechanical modeling of rupture around metamictic minerals; 33 - Helium diffusion in apatite: Effect alpha recoil-linked damages; 34 - Rare earth spectra in uranium oxides: a marker of the uranium deposit type; 35 - Rare earths: tracers of uranium behaviour during acid sulphated hydrothermal weathering - the Guadeloupe example; 36 - What metallogenic model for the Kiggavik-Andrew Lake trend? Nunavut, Canada; 37 - Uranium mobility in the Southern

  18. Uranium, depleted uranium, biological effects; Uranium, uranium appauvri, effets biologiques

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2001-07-01

    Physicists, chemists and biologists at the CEA are developing scientific programs on the properties and uses of ionizing radiation. Since the CEA was created in 1945, a great deal of research has been carried out on the properties of natural, enriched and depleted uranium in cooperation with university laboratories and CNRS. There is a great deal of available data about uranium; thousands of analyses have been published in international reviews over more than 40 years. This presentation on uranium is a very brief summary of all these studies. (author)

  19. Uranium toxicology

    International Nuclear Information System (INIS)

    Ferreyra, Mariana D.; Suarez Mendez, Sebastian

    1997-01-01

    In this paper are presented the methods and procedures optimized by the Nuclear Regulatory Authority (ARN) for the determination of: natural uranium mass, activity of enriched uranium in samples of: urine, mucus, filters, filter heads, rinsing waters and Pu in urine, adopted and in some cases adapted, by the Environmental Monitoring and Internal Dosimetry Laboratory. The analyzed material corresponded to biological and environmental samples belonging to the staff professionally exposed that work in plants of the nuclear fuel cycle. For a better comprehension of the activities of this laboratory, it is included a brief description of the uranium radiochemical toxicity and the limits internationally fixed to preserve the workers health

  20. Characterization of Cu–Ni nanostructured alloys obtained by a chemical route. Influence of the complexing agent content in the starting solution

    Energy Technology Data Exchange (ETDEWEB)

    Carreras, Alejo C., E-mail: acarreras@famaf.unc.edu.ar [Instituto de Física Enrique Gaviola (IFEG), Facultad de Matemática, Astronomía y Física, Universidad Nacional de Córdoba—CONICET, Medina Allende s/n, Ciudad Universitaria, 5016 Córdoba (Argentina); Cangiano, María de los A.; Ojeda, Manuel W.; Ruiz, María del C. [Instituto de Investigaciones en Tecnología Qumica (INTEQUI), Facultad de Química, Bioquímica y Farmacia, Universidad Nacional de San Luis—CONICET, Chacabuco y Pedernera, 5700 San Luis (Argentina)

    2015-03-15

    The influence of the amount of complexing agent added to the starting solution on the physicochemical properties of Cu–Ni nanostructured alloys obtained through a chemical route, was studied. For this purpose, three Cu–Ni nanoalloy samples were synthesized by a previously developed procedure, starting from solutions with citric acid to metal molar ratios (C/Me) of 0.73, 1.00 and 1.50. The synthesis technique consisted in preparing a precursor via the citrate-gel method, and carrying out subsequent thermal treatments in controlled atmospheres. Sample characterization was performed by scanning electron microscopy, X-ray microanalysis, X-ray diffraction, transmission electron microscopy, X-ray nanoanalysis and electron diffraction. In the three cases, copper and nickel formed a solid solution with a Cu/Ni atomic ratio close to 50/50, and free of impurities inside the crystal structure. The citric acid content of the starting solution proved to have an important influence on the morphology, size distribution, porosity, and crystallinity of the Cu–Ni alloy microparticles obtained, but a lesser influence on their chemical composition. The molar ratio C/Me = 1.00 resulted in the alloy with the Cu/Ni atomic ratio closest to 50/50. - Highlights: • We synthesize Cu–Ni nanoalloys by a chemical route based on the citrate-gel method. • We study the influence of the complexing agent content of the starting solution. • We characterize the samples by electron microscopy and X-ray techniques. • Citric acid influences the shape, size, porosity and crystallinity of the alloys.

  1. Uranium metallogenesis of the peraluminous leucogranite from the Pontivy-Rostrenen magmatic complex (French Armorican Variscan belt): the result of long-term oxidized hydrothermal alteration during strike-slip deformation

    Science.gov (United States)

    Ballouard, C.; Poujol, M.; Mercadier, J.; Deloule, E.; Boulvais, P.; Baele, J. M.; Cuney, M.; Cathelineau, M.

    2018-06-01

    In the French Armorican Variscan belt, most of the economically significant hydrothermal U deposits are spatially associated with peraluminous leucogranites emplaced along the south Armorican shear zone (SASZ), a dextral lithospheric scale wrench fault that recorded ductile deformation from ca. 315 to 300 Ma. In the Pontivy-Rostrenen complex, a composite intrusion, the U mineralization is spatially associated with brittle structures related to deformation along the SASZ. In contrast to monzogranite and quartz monzodiorite (3 3), the leucogranite samples are characterized by highly variable U contents ( 3 to 27 ppm) and Th/U ratios ( 0.1 to 5) suggesting that the crystallization of magmatic uranium oxide in the more evolved facies was followed by uranium oxide leaching during hydrothermal alteration and/or surface weathering. U-Pb dating of uranium oxides from the deposits reveals that they mostly formed between ca. 300 and 270 Ma. In monzogranite and quartz monzodiorite, apatite grains display magmatic textures and provide U-Pb ages of ca. 315 Ma reflecting the time of emplacement of the intrusions. In contrast, apatite grains from the leucogranite display textural, geochemical, and geochronological evidences for interaction with U-rich oxidized hydrothermal fluids contemporaneously with U mineralizing events. From 300 to 270 Ma, infiltration of surface-derived oxidized fluids leached magmatic uranium oxide from fertile leucogranite and formed U deposits. This phenomenon was sustained by brittle deformation and by the persistence of thermal anomalies associated with U-rich granitic bodies.

  2. Complexation study of a tert-butyl-calix[4]arene-based 2-hydroxynaphthalene ligand with uranium(VI) in non-aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Bauer, Anne; Schmeide, Katja [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Surface Processes

    2017-06-01

    The actinide uranium, well known from nuclear power cycle, plays also a role in rare earth production as it is an undesired constituent of the respective ores. To facilitate the production of rare earth elements, uranium has to be removed. Due to their modifiable selectivity and solubility calix[n]arenes are interesting compounds for the extraction of actinides and lanthanides. The mechanism of uranium(VI) interaction with a tert-butyl-calix[4]arene-based 2-hydroxynaphthalene ligand (L1) was studied by TRLFS, UV-vis spectroscopy and isothermal calorimetry.

  3. Why can rossing uranium mine keep mining even in low price conditions of uranium market

    International Nuclear Information System (INIS)

    Tan Chenglong

    2004-01-01

    Rossing uranium mine is the only operating uranium mine in the world where the uranium occurs in intrusive alaskite. In the past 10 years, uranium market regressed in the world, uranium production weakened, expenditures of capital for uranium exploration were insufficient. Uranium spot market price rapidly decreased from $111.8/kg U in late 1970's to $22.1/kg U in mid-1990's. Why can Rossing uranium mine mined with traditional underground and open pit operation can keep running even in low price conditions of uranium market? Augumenting research on the deposit, mineral and technology, decreasing production cost and improving selling strategy can not only maintain Rossing's uranium production at present, but also ensure sustainable development in the coming 15 years. Exploration of low-costed uranium deposits is very important. However, obvious economic benefits can be obtained, as Rossing uranium mine does, by augumenting geological-economical research on the known uranium deposits of hard-rock type and by using new techniques to improve the conventional techniques in the uranium mine development. (authors)

  4. Rossing uranium

    International Nuclear Information System (INIS)

    Anon.

    1979-01-01

    In this article the geology of the deposits of the Rossing uranium mine in Namibia is discussed. The planning of the open-pit mining, the blasting, drilling, handling and the equipment used for these processes are described

  5. Investigation of uranium binding forms in environmentally relevant waters and bio-fluids

    International Nuclear Information System (INIS)

    Osman, Alfatih Ahmed Alamin

    2014-01-01

    Uranium from natural and anthropogenic sources is continuously and increasingly released into the environment, enters the food chain, and eventually accumulates into the bio-systems including humans. Therefore, uranium exposure to human becomes more and more a subject of interest in many scientific disciplines such as environmental medicine, toxicology, and radiation protection. Ingestion of uranium via food and drinking water is one of the important pathways of exposure. The ongoing discussion in Germany and the European Union (EU) on the maximum uranium levels in drinking water reflects the increasing awareness of uranium as a public health problem. For water suppliers in many countries around the world, uranium contamination of drinking water also becomes a salient issue. Nevertheless, the health consequences are dependent not only on the level and duration of exposure, but mainly on the physical and chemical forms of uranium (speciation). Unlike total concentration, speciation can provide more information on uranium behavior (mobility, bioavailability, and toxicity) in both geo-systems and bio-systems. The aim of the current work is to elucidate uranium speciation in natural samples (water, bio-fluids) by both spectroscopic means and theoretical modeling. For this purpose, environmentally relevant waters (mineral water, groundwater, acid drainage waters) and natural human body fluids have been investigated. The cryogenic time-resolved laser-induced fluorescence spectroscopy (cryo-TRLFS) at 153 K has successfully been used to identify the speciation in such complex matrices of high organic content and low uranium concentrations without any prior treatment. Data about uranium binding forms in natural waters could be used for more insight research on uranium chemo-toxicity in drinking water since there is no available information on the long-term exposure of low uranium concentrations via ingestion on humans. Altogether the obtained data provides a comprehensive

  6. Investigation of uranium binding forms in environmentally relevant waters and bio-fluids

    Energy Technology Data Exchange (ETDEWEB)

    Osman, Alfatih Ahmed Alamin

    2014-06-04

    Uranium from natural and anthropogenic sources is continuously and increasingly released into the environment, enters the food chain, and eventually accumulates into the bio-systems including humans. Therefore, uranium exposure to human becomes more and more a subject of interest in many scientific disciplines such as environmental medicine, toxicology, and radiation protection. Ingestion of uranium via food and drinking water is one of the important pathways of exposure. The ongoing discussion in Germany and the European Union (EU) on the maximum uranium levels in drinking water reflects the increasing awareness of uranium as a public health problem. For water suppliers in many countries around the world, uranium contamination of drinking water also becomes a salient issue. Nevertheless, the health consequences are dependent not only on the level and duration of exposure, but mainly on the physical and chemical forms of uranium (speciation). Unlike total concentration, speciation can provide more information on uranium behavior (mobility, bioavailability, and toxicity) in both geo-systems and bio-systems. The aim of the current work is to elucidate uranium speciation in natural samples (water, bio-fluids) by both spectroscopic means and theoretical modeling. For this purpose, environmentally relevant waters (mineral water, groundwater, acid drainage waters) and natural human body fluids have been investigated. The cryogenic time-resolved laser-induced fluorescence spectroscopy (cryo-TRLFS) at 153 K has successfully been used to identify the speciation in such complex matrices of high organic content and low uranium concentrations without any prior treatment. Data about uranium binding forms in natural waters could be used for more insight research on uranium chemo-toxicity in drinking water since there is no available information on the long-term exposure of low uranium concentrations via ingestion on humans. Altogether the obtained data provides a comprehensive

  7. Process for recovering uranium

    Science.gov (United States)

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

    1959-03-24

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

  8. Uranium extraction from seawater

    International Nuclear Information System (INIS)

    Bals, H.G.

    1976-03-01

    After an introduction to the physics and chemistry of the sea and an estimation of the chances for the absorption of uranium from rivers, the material-sepecific characteristics of the adsorber technology are decribed in detail. Then, the methods used for gaining uranium form seawater are described with special regard to the tidal and the so-called serial (sequency) method. Whether all methods described can be realised is an economic problem since very high quantitics of water are necessary because of the low contents of uranium. A positive energy balance (gained energy/lost energy) is not definitely ensured yet for the production methods used. The development measures to be taken to obtain a positive energy balance are briefly described, and the research programme of the UEBG is mentioned. (UA) [de

  9. Control of the formation Yield of complex with DTPA and DOTATATE of the Chloride of 90Y taken place in CENTIS for the obtaining of Radiopharmaceutical

    International Nuclear Information System (INIS)

    Soler Iglesias, Joel; Serra Aguila, Rolando; Morín Zorrilla, José; Pino Peraza, Madián; Alberti Ramírez, Alejandro; Turiño Perez, David

    2016-01-01

    Issuing beta pure with period of semidesintegration of 64,1 hours and 2,28 MeV of energy, the 90Y are useful as therapeutic radionuclide. Radiopharmaceuticals 90Y has been effective in the treatment of chronic synovitis, liver cancer, pain for bony metastasis and tumors of origin neuroendocrine. They are of particular interest the results obtained in the treatment of the lymphomas no-Hodgkin that combine the specificity of an antibody monoclonal for the antigen CD20 and the energy pure beta of the 90Y. It could be verified that for their content of 90Sr similar to 0,110 ± 0,004 (k = 2) kBq / g carried out by different methods and their combination capacity with DTPA And DOTATATE, chelate bifunctional in appropriate range of concentrations and in presence of metallic appearances, it is of excellent characteristics for their use as precursor in the obtaining of therapeutic, included radiopharmaceuticals the radioimmunotherapy. The presence of Faith (III) was studied in details by the addition method and it could be determined that it only affects the yield of labeling of 90Y with DTPA if its presence is superior to a concentration of 0,018 µ mol / L. It is demonstrated that the presence of other metals like Pb (II), Zn (II) and Cu (II) also influence significantly in the yield of included complexation in excess presence of the tying bifunctional. (author)

  10. Uranium extraction in phosphoric acid

    International Nuclear Information System (INIS)

    Araujo Figueiredo, C. de

    1984-01-01

    Uranium is recovered from the phosphoric liquor produced from the concentrate obtained from phosphorus-uraniferous mineral from Itataia mines (CE, Brazil). The proposed process consists of two extraction cycles. In the first one, uranium is reduced to its tetravalent state and then extracted by dioctylpyrophosphoric acid, diluted in Kerosene. Re-extraction is carried out with concentrated phosphoric acid containing an oxidising agent to convert uranium to its hexavalent state. This extract (from the first cycle) is submitted to the second cycle where uranium is extracted with DEPA-TOPO (di-2-hexylphosphoric acid/tri-n-octyl phosphine oxide) in Kerosene. The extract is then washed and uranium is backextracted and precipitated as commercial concentrate. The organic phase is recovered. Results from discontinuous tests were satisfactory, enabling to establish operational conditions for the performance of a continuous test in a micro-pilot plant. (Author) [pt

  11. Uranium, depleted uranium, biological effects

    International Nuclear Information System (INIS)

    2001-01-01

    Physicists, chemists and biologists at the CEA are developing scientific programs on the properties and uses of ionizing radiation. Since the CEA was created in 1945, a great deal of research has been carried out on the properties of natural, enriched and depleted uranium in cooperation with university laboratories and CNRS. There is a great deal of available data about uranium; thousands of analyses have been published in international reviews over more than 40 years. This presentation on uranium is a very brief summary of all these studies. (author)

  12. Stability effect of cholesterol-poly(acrylic acid) in a stimuli-responsive polymer-liposome complex obtained from soybean lecithin for controlled drug delivery.

    Science.gov (United States)

    Simões, M G; Alves, P; Carvalheiro, Manuela; Simões, P N

    2017-04-01

    The development of polymer-liposome complexes (PLCs), in particular for biomedical applications, has grown significantly in the last decades. The importance of these studies comes from the emerging need in finding intelligent controlled release systems, more predictable, effective and selective, for applications in several areas, such as treatment and/or diagnosis of cancer, neurological, dermatological, ophthalmic and orthopedic diseases, gene therapy, cosmetic treatments, and food engineering. This work reports the development and characterization of a pH sensitive system for controlled release based on PLCs. The selected hydrophilic polymer was poly(acrylic acid) (PAA) synthesized by atom transfer radical polymerization (ATRP) with a cholesterol (CHO) end-group to improve the anchoring of the polymer into the lipid bilayer. The polymer was incorporated into liposomes formulated from soybean lecithin and stearylamine, with different stearylamine/phospholipid and polymer/phospholipid ratios (5, 10 and 20%). The developed PLCs were characterized in terms of particle size, polydispersity, zeta potential, release profiles, and encapsulation efficiency. Cell viability studies were performed to assess the cytotoxic potential of PLCs. The results showed that the liposomal formulation with 5% of stearylamine and 10% of polymer positively contribute to the stabilization of the complexes. Afterwards, the carboxylic acid groups of the polymer present at the surface of the liposomes were crosslinked and the same parameters analyzed. The crosslinked complexes showed to be more stable at physiologic conditions. In addition, the release profiles at different pHs (2-12) revealed that the obtained complexes released all their content at acidic conditions. In summary, the main accomplishments of this work are: (i) innovative synthesis of cholesterol-poly(acrylic acid) (CHO-PAA) by ATRP; (ii) stabilization of the liposomal formulation by incorporation of stearylamine and CHO

  13. Uranium loans

    International Nuclear Information System (INIS)

    Anon.

    1990-01-01

    When NUEXCO was organized in 1968, its founders conceived of a business based on uranium loans. The concept was relatively straightforward; those who found themselves with excess supplies of uranium would deposit those excesses in NUEXCO's open-quotes bank,close quotes and those who found themselves temporarily short of uranium could borrow from the bank. The borrower would pay interest based on the quantity of uranium borrowed and the duration of the loan, and the bank would collect the interest, deduct its service fee for arranging the loan, and pay the balance to those whose deposits were borrowed. In fact, the original plan was to call the firm Nuclear Bank Corporation, until it was discovered that using the word open-quotes Bankclose quotes in the name would subject the firm to various US banking regulations. Thus, Nuclear Bank Corporation became Nuclear Exchange Corporation, which was later shortened to NUEXCO. Neither the nuclear fuel market nor NUEXCO's business developed quite as its founders had anticipated. From almost the very beginning, the brokerage of uranium purchases and sales became a more significant activity for NUEXCO than arranging uranium loans. Nevertheless, loan transactions have played an important role in the international nuclear fuel market, requiring the development of special knowledge and commercial techniques

  14. United States uranium enrichment policies

    International Nuclear Information System (INIS)

    Roberts, R.W.

    1977-01-01

    ERDA's uranium enrichment program policies governing the manner in which ERDA's enrichment complex is being operated and expanded to meet customer requirements for separative work, research and development activities directed at providing technology alternatives for future enrichment capacity, and establishing the framework for additional domestic uranium enrichment capacity to meet the domestic and foreign nuclear industry's growing demand for enrichment services are considered. The ERDA enrichment complex consists of three gaseous diffusion plants located in Oak Ridge, Tennessee; Paducah, Kentucky; and Portsmouth, Ohio. Today, these plants provide uranium enrichment services for commercial nuclear power generation. These enrichment services are provided under contracts between the Government and the utility customers. ERDA's program involves a major pilot plant cascade, and pursues an advanced isotope separation technique for the late 1980's. That the United States must develop additional domestic uranium enrichment capacity is discussed

  15. Preparation of UO_2 Fine Particle by Hydrolysis of Uranium(IV) Alkoxide

    OpenAIRE

    Satoh, Isamu; Takahashi, Mitsuyuki; Miura, Shigeyuki

    1997-01-01

    Fine particles of uranium(IV) dioxides were obtained by hydrolysis of uranium(IV) ethoxide which was synthesized by reacting uranium tetrachloride with sodium ethoxide. The monodispersed submicrometer particles were confirmed by SEM observation.

  16. Ionic flotation of uranium contained in industrial phosphoric acid

    International Nuclear Information System (INIS)

    Jdid; Blazy; Bessiere

    1983-01-01

    A new process for uranium recovery from industrial phosphoric acid at 30% of P 2 O 5 is applied by the ionic flotation process. Research is carried out on determination of the nature of ionic species of U in H 3 PO 4 5.5 M and the behavior of reagents from CECA Co. in very acid media. Reagents able to form complexes directly with uranium and stable in phosphoric acid selected are: potassium ethylene diamine tetra (methylene phosphonate) (INIPOL AD32) and sodium dialkyldiphosphonate (34S). Uranium IV, obtained by reduction of uranium VI with iron powder, is precipitated by these reagents. Flotation of the precipitate obtained with INIPOL AD 32 is realized by addition of hexylamino bis (methylene phosphonic acid). A recovery of 80 wt% is obtained. Flotation of the coprecipitate 34S-U(IV) is obtained without any other additions because 34S is a surfactant. Metal recovery is better than 90% and the coprecipitate contains more than 10% U. The process is fast precipitation 10 minutes and flotation 5 minutes and is efficient even at 60 0 C [fr

  17. Solubility measurement of uranium in uranium-contaminated soils

    International Nuclear Information System (INIS)

    Lee, S.Y.; Elless, M.; Hoffman, F.

    1993-08-01

    A short-term equilibration study involving two uranium-contaminated soils at the Fernald site was conducted as part of the In Situ Remediation Integrated Program. The goal of this study is to predict the behavior of uranium during on-site remediation of these soils. Geochemical modeling was performed on the aqueous species dissolved from these soils following the equilibration study to predict the on-site uranium leaching and transport processes. The soluble levels of total uranium, calcium, magnesium, and carbonate increased continually for the first four weeks. After the first four weeks, these components either reached a steady-state equilibrium or continued linearity throughout the study. Aluminum, potassium, and iron, reached a steady-state concentration within three days. Silica levels approximated the predicted solubility of quartz throughout the study. A much higher level of dissolved uranium was observed in the soil contaminated from spillage of uranium-laden solvents and process effluents than in the soil contaminated from settling of airborne uranium particles ejected from the nearby incinerator. The high levels observed for soluble calcium, magnesium, and bicarbonate are probably the result of magnesium and/or calcium carbonate minerals dissolving in these soils. Geochemical modeling confirms that the uranyl-carbonate complexes are the most stable and dominant in these solutions. The use of carbonate minerals on these soils for erosion control and road construction activities contributes to the leaching of uranium from contaminated soil particles. Dissolved carbonates promote uranium solubility, forming highly mobile anionic species. Mobile uranium species are contaminating the groundwater underlying these soils. The development of a site-specific remediation technology is urgently needed for the FEMP site

  18. Estimation of uranium forms in oceanic water

    International Nuclear Information System (INIS)

    Krylov, O.T.; Novikov, P.D.; Nesterova, M.P.

    1985-01-01

    A critical consideration is given to the notions about uranium forms in ocean water. To estimate uranium forms a model is suggested which takes into account possjble formation of complexes of uranyl ions and ocean water anions Cl - , SO 4 2- , CO 3 2- , HCO 3 - , OH - , F - . The available published data are used to estimate necessary thermodynamic stability constants of the complexes, activity coefficients and concentration of componenets. The thermodynamic calculation shows that uranium hydroxocomplex compounds UO 2 (OH) 4 2- (99.17%) and UO 2 (OH) 3 - (083%) are the most probable uranium forms in ocear water of 34.3% salinity at 25 deg C and 1 atm pressure

  19. Geochemical methods for identification of formations being prospective for uranium

    International Nuclear Information System (INIS)

    Zhukova, A.M.; Komarova, N.I.; Spiridonov, A.A.; Shor, G.M.

    1985-01-01

    Geochemical methods of uranium content evaluation in metamorphic, ultrametamorphic and sedimentary formations are considered. At that, the following four factors are of the highest importance: 1) average uranium content-geochemical background; 2) character of uranium distribution; 3) forms of uranium presence; 4) the value of thorium-uranium ratio. A complex of radiogeochemical criteria, favourable for uranium presence is formulated: high average background content of total and '' mobile''uranium and high value of variation coefficient (80-100% and above); low (approximately one or lower) thorium-uranium ratio; sharp increase in uranium concentration in accessory minerals. Radiogeochemical peculiarities of metamorphic and ultrametamorphic formations prospective for uranium are enumerated. The peculiarities condition specificity of geochemical prospecting methods. Prospecting methods first of all must be directed at the evaluation of radioelement distribution parameters and specification of the forms of their presence

  20. Standard specification for uranium metal enriched to more than 15 % and less Than 20 % 235U

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2000-01-01

    1.1 This specification covers nuclear grade uranium metal that has either been processed through an enrichment plant, or has been produced by the blending of highly enriched uranium with other uranium, to obtain uranium of any 235U concentration below 20 % (and greater than 15 %) and that is intended for research reactor fuel fabrication. The scope of this specification includes specifications for enriched uranium metal derived from commercial natural uranium, recovered uranium, or highly enriched uranium. Commercial natural uranium, recovered uranium and highly enriched uranium are defined in Section 3. The objectives of this specification are to define the impurity and uranium isotope limits for commercial grade enriched uranium metal. 1.2 This specification is intended to provide the nuclear industry with a standard for enriched uranium metal which is to be used in the production of research reactor fuel. In addition to this specification, the parties concerned may agree to other appropriate conditions. ...

  1. Uranium ore deposits: geology and processing implications

    International Nuclear Information System (INIS)

    Belyk, C.L.

    2010-01-01

    There are fifteen accepted types of uranium ore deposits and at least forty subtypes readily identified around the world. Each deposit type has a unique set of geological characteristics which may also result in unique processing implications. Primary uranium production in the past decade has predominantly come from only a few of these deposit types including: unconformity, sandstone, calcrete, intrusive, breccia complex and volcanic ones. Processing implications can vary widely between and within the different geological models. Some key characteristics of uranium deposits that may have processing implications include: ore grade, uranium and gangue mineralogy, ore hardness, porosity, uranium mineral morphology and carbon content. Processing difficulties may occur as a result of one or more of these characteristics. In order to meet future uranium demand, it is imperative that innovative processing approaches and new technological advances be developed in order that many of the marginally economic traditional and uneconomic non-traditional uranium ore deposits can be exploited. (author)

  2. The significance of zircon characteristic and its uranium concentration in evaluation of uranium metallogenetic prospect

    International Nuclear Information System (INIS)

    Li Yaosong; Zhu Jiechen; Xia Yuliang

    1992-02-01

    Zircon characteristic and its relation to uranium metallogenetic process have been studied on the basis of physics properties and chemical compositions. It is indicated that the colour of zircon crystal is related to uranium concentration; on the basis of method of zircon population type of Pupin J.P., the sectional plan of zircon population type has been designed, from which result that zircon population type of uranium-producing rock body is distributed mainly in second section, secondly in fourth section; U in zircon presents synchronous increase trend with Th, Hf and Ta; the uranium concentration in zircon from uranium-producing geologic body increases obviously and its rate of increase is more than that of the uranium concentration in rock; the period, in which uranium concentration in zircon is increased, is often related to better uranium-producing condition in that period of this area. 1785 data of the average uranium concentration in zircon have been counted and clear regularity has been obtained, namely the average uranium concentrations in zircon in rich uranium-producing area, rock, geologic body and metallogenetic zone are all higher than that in poor or no uranium-producing area, rock, geologic body and metallogenetic zone. This shows that the average uranium concentration in zircon within the region in fact reflects the primary uranium-bearing background in region and restricts directly follow-up possibility of uranium mineralization. On the basis of this, the uranium source conditions of known uranium metallogenetic zones and prospective provinces have been discussed, and the average uranium concentrations in zircon from magmatic rocks for 81 districts have been contrasted and graded, and some districts in which exploration will be worth doing further are put forward

  3. Synthesis of Uranium nitride powders using metal uranium powders

    International Nuclear Information System (INIS)

    Yang, Jae Ho; Kim, Dong Joo; Oh, Jang Soo; Rhee, Young Woo; Kim, Jong Hun; Kim, Keon Sik

    2012-01-01

    Uranium nitride (UN) is a potential fuel material for advanced nuclear reactors because of their high fuel density, high thermal conductivity, high melting temperature, and considerable breeding capability in LWRs. Uranium nitride powders can be fabricated by a carbothermic reduction of the oxide powders, or the nitriding of metal uranium. The carbothermic reduction has an advantage in the production of fine powders. However it has many drawbacks such as an inevitable engagement of impurities, process burden, and difficulties in reusing of expensive N 15 gas. Manufacturing concerns issued in the carbothermic reduction process can be solved by changing the starting materials from oxide powder to metals. However, in nitriding process of metal, it is difficult to obtain fine nitride powders because metal uranium is usually fabricated in the form of bulk ingots. In this study, a simple reaction method was tested to fabricate uranium nitride powders directly from uranium metal powders. We fabricated uranium metal spherical powder and flake using a centrifugal atomization method. The nitride powders were obtained by thermal treating those metal particles under nitrogen containing gas. We investigated the phase and morphology evolutions of powders during the nitriding process. A phase analysis of nitride powders was also a part of the present work

  4. Uranium extraction from gold-uranium ores

    Energy Technology Data Exchange (ETDEWEB)

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

    1981-01-01

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

  5. Flotation of uranium from uranium ores in Canada. Part 1

    International Nuclear Information System (INIS)

    Muthuswami, S.V.; Vigayan, S.; Woods, D.R.; Banerjee, S.

    1983-01-01

    About 150 flotation tests were done on Elliot Lake ore with 15 reagents as collectors in order to screen and choose an attractive collector for uranium flotation. Several variables were studied including pH, conditioning time and mode of collector addition. The tests were done in a Denver or Agitair subaeration cell. The particle size of the ore was kept at 85% below -325 mesh. Three reagents (Kelex 00, TOPO, and cupferron) were identified as having the most promise. The best results were obtained with cupferron, where 93-95% of the uranium was recovered in 25-30% of the mass of original ore. Radium in the tails varied between 5 and 30 pCi/g depending on the mass of uranium floated. Radium was recovered in proportion to uranium in the tests done at neutral pH. The preconcentration results obtained by flotation alone were comparable to those obtained using pyrite flotation and wet high-intensity magnetic separation of uranium. The consumption of cupferron was 4 kg/Mg ore for each flotation stage. This was 10-15 times larger than the collector usage in conventional oxide flotation. This scheme did not require other reagents as depressants, activators or modifiers. Reproducibility was good and similar recoveries were obtained with fresh or old ores, and with distilled or mine water. The selectivity of cupferron for uranium in the ore studied was outstanding

  6. Enhancement of Extraction of Uranium from Seawater

    Energy Technology Data Exchange (ETDEWEB)

    Al-Sheikhly, Mohamad [Univ. of Maryland, College Park, MD (United States); Dietz, Travis [Univ. of Maryland, College Park, MD (United States); Tsinas, Zois [Univ. of Maryland, College Park, MD (United States); Tomaszewski, Claire [Univ. of Maryland, College Park, MD (United States); Pazos, Ileana M. [Univ. of Maryland, College Park, MD (United States); Nigliazzo, Olga [The Catholic Univ. of America, Washington, DC (United States); Li, Weixing [The Catholic Univ. of America, Washington, DC (United States); Adel-Hadadi, Mohamad [Univ. of Maryland, College Park, MD (United States); Barkatt, Aaron [Univ. of Palermo (Italy)

    2016-04-01

    Even at a concentration of 3 μg/L, the world’s oceans contain a thousand times more uranium than currently know terrestrial sources. In order to take advantage of this stockpile, methods and materials must be developed to extract it efficiently, a difficult task considering the very low concentration of the element and the competition for extraction by other atoms in seawater such as sodium, calcium, and vanadium. The majority of current research on methods to extract uranium from seawater are vertical explorations of the grafting of amidoxime ligand, which was originally discovered and promoted by Japanese studies in the late 1980s. Our study expands on this research horizontally by exploring the effectiveness of novel uranium extraction ligands grafted to the surface of polymer substrates using radiation. Through this expansion, a greater understanding of uranium binding chemistry and radiation grafting effects on polymers has been obtained. While amidoxime-functionalized fabrics have been shown to have the greatest extraction efficiency so far, they suffer from an extensive chemical processing step which involves treatment with powerful basic solutions. Not only does this add to the chemical waste produced in the extraction process and add to the method’s complexity, but it also significantly impacts the regenerability of the amidoxime fabric. The approach of this project has been to utilize alternative, commercially available monomers capable of extracting uranium and containing a carbon-carbon double bond to allow it to be grafted using radiation, specifically phosphate, oxalate, and azo monomers. The use of commercially available monomers and radiation grafting with electron beam or gamma irradiation will allow for an easily scalable fabrication process once the technology has been optimized. The need to develop a cheap and reliable method for extracting uranium from seawater is extremely valuable to energy independence and will extend the quantity of

  7. Enhancement of Extraction of Uranium from Seawater

    International Nuclear Information System (INIS)

    Al-Sheikhly, Mohamad; Dietz, Travis; Tsinas, Zois; Tomaszewski, Claire; Pazos, Ileana M.; Nigliazzo, Olga; Li, Weixing; Adel-Hadadi, Mohamad; Barkatt, Aaron

    2016-01-01

    Even at a concentration of 3 @@g/L, the world@@@s oceans contain a thousand times more uranium than currently know terrestrial sources. In order to take advantage of this stockpile, methods and materials must be developed to extract it efficiently, a difficult task considering the very low concentration of the element and the competition for extraction by other atoms in seawater such as sodium, calcium, and vanadium. The majority of current research on methods to extract uranium from seawater are vertical explorations of the grafting of amidoxime ligand, which was originally discovered and promoted by Japanese studies in the late 1980s. Our study expands on this research horizontally by exploring the effectiveness of novel uranium extraction ligands grafted to the surface of polymer substrates using radiation. Through this expansion, a greater understanding of uranium binding chemistry and radiation grafting effects on polymers has been obtained. While amidoxime-functionalized fabrics have been shown to have the greatest extraction efficiency so far, they suffer from an extensive chemical processing step which involves treatment with powerful basic solutions. Not only does this add to the chemical waste produced in the extraction process and add to the method@@@s complexity, but it also significantly impacts the regenerability of the amidoxime fabric. The approach of this project has been to utilize alternative, commercially available monomers capable of extracting uranium and containing a carbon-carbon double bond to allow it to be grafted using radiation, specifically phosphate, oxalate, and azo monomers. The use of commercially available monomers and radiation grafting with electron beam or gamma irradiation will allow for an easily scalable fabrication process once the technology has been optimized. The need to develop a cheap and reliable method for extracting uranium from seawater is extremely valuable to energy independence and will extend the quantity of

  8. Determination and interpretation of environmental water samples contaminated by uranium mining activities

    International Nuclear Information System (INIS)

    Meinrath, G.; Volke, P.; Helling, C.; Merkel, B.J.; Dudel, E.G.

    1999-01-01

    Interpretation of environmental behavior of uranium is based on several steps of data analysis and statistical inference. First step is sampling and analyzing of uranium in field samples by routine laboratory methods. Such methods have to fulfill multiple requirements like robustness, efficiency, low detection limit and precision. A comparison of different approaches in assigning uncertainty to experimentally obtained analytical data shows that classical error estimation is not significantly inferior to more sophisticated modern techniques like inverse regression or orthogonal regression. A second step is the correlation of analytical data with current state of insight into environmental behavior of uranium. Such a correlation furthers the choice of adequate geochemical models and quality of geochemical data base for subsequent detailed analysis, e.g. by geochemical modeling. An appraisal of the individual steps in this complex analysis is given on the basis of statistical procedures for calibration and an E H -pH diagram of uranium for atmospheric conditions. (orig.)

  9. Microparticles obtained by complex coacervation: influence of the type of reticulation and the drying process on the release of the core material

    Directory of Open Access Journals (Sweden)

    Izabela Dutra Alvim

    2010-12-01

    Full Text Available Microparticles obtained by complex coacervation were crosslinked with glutaraldehyde or with transglutaminase and dried using freeze drying or spray drying. Moist samples presented Encapsulation Efficiency (%EE higher than 96%. The mean diameters ranged from 43.7 ± 3.4 to 96.4 ± 10.3 µm for moist samples, from 38.1 ± 5.36 to 65.2 ± 16.1 µm for dried samples, and from 62.5 ± 7.5 to 106.9 ± 26.1 µm for rehydrated microparticles. The integrity of the particles without crosslinking was maintained when freeze drying was used. After spray drying, only crosslinked samples were able to maintain the wall integrity. Microparticles had a round shape and in the case of dried samples rugged walls apparently without cracks were observed. Core distribution inside the particles was multinuclear and homogeneous and core release was evaluated using anhydrous ethanol. Moist particles crosslinked with glutaraldehyde at the concentration of 1.0 mM.g-1 protein (ptn, were more efficient with respect to the core retention compared to 0.1 mM.g-1 ptn or those crosslinked with transglutaminase (10 U.g-1 ptn. The drying processes had a strong influence on the core release profile reducing the amount released to all dry samples

  10. Use of tetracycline as complexing agent in analytical chemistry

    International Nuclear Information System (INIS)

    Nastasi, M.J.C.; Saiki, M.; Lima, F.W.

    1977-01-01

    The behavior of tetracyline as complexing agent in solvent extraction studies is presented. The extraction curves for the lanthanide elements, scandium, thorium, uranium and neptunium, are determined for the extraction system benzyl alcohol-tetracycline, as well as the acid and extractant dependences of extraction of the lanthanide elements. Separation of neptunium from uranium is formed by carrying out the extraction experiment at a proper pH value. Use is made of masking agents namely, ethylenediaminetetraacetic acid (EDTA) and diethylenetriaminepentaacetic acid (DTPA), in order to obtain separations of uranium from scadium and lanthanides as well as of uranium and thorium, respectively. The extraction experiments are carried out by using radioisotopes of each element, except for uranium in which case the determinations are by using epithermal neutron activation analysis [pt

  11. Uranium enrichment

    International Nuclear Information System (INIS)

    Rae, H.K.; Melvin, J.G.

    1988-06-01

    Canada is the world's largest producer and exporter of uranium, most of which is enriched elsewhere for use as fuel in LWRs. The feasibility of a Canadian uranium-enrichment enterprise is therefore a perennial question. Recent developments in uranium-enrichment technology, and their likely impacts on separative work supply and demand, suggest an opportunity window for Canadian entry into this international market. The Canadian opportunity results from three particular impacts of the new technologies: 1) the bulk of the world's uranium-enrichment capacity is in gaseous diffusion plants which, because of their large requirements for electricity (more than 2000 kW·h per SWU), are vulnerable to competition from the new processes; 2) the decline in enrichment costs increases the economic incentive for the use of slightly-enriched uranium (SEU) fuel in CANDU reactors, thus creating a potential Canadian market; and 3) the new processes allow economic operation on a much smaller scale, which drastically reduces the investment required for market entry and is comparable with the potential Canadian SEU requirement. The opportunity is not open-ended. By the end of the century the enrichment supply industry will have adapted to the new processes and long-term customer/supplier relationships will have been established. In order to seize the opportunity, Canada must become a credible supplier during this century

  12. Method for electrodeposition of nickel--chromium alloys and coating of uranium

    International Nuclear Information System (INIS)

    Stromatt, R.W.; Lundquist, J.R.

    1975-01-01

    High-quality electrodeposits of nickel-chromium binary alloys in which the percentage of chromium is controlled can be obtained by the addition of a complexing agent such as ethylenediaminetetraacetic disodium salt to the plating solution. The nickel-chromium alloys were found to provide an excellent hydrogen barrier for the protection of uranium fuel elements. (U.S.)

  13. Electrical impedance studies of uranium oxide

    International Nuclear Information System (INIS)

    Hampton, R.N.

    1986-11-01

    The thesis presents data on the electrical properties of uranium oxide at temperatures from 1700K to 4.2K, and pressures between 25 K bar and 70 K bar. The impedance data were analysed using the technique of complex plane representation to establish the conductivity and dielectric constant of uranium dioxide. The thermophysical data were compared with previously reported experimental and theoretical work on uranium dioxide and other fluorite structured oxides. (U.K.)

  14. Liquid membrane process for uranium recovery

    International Nuclear Information System (INIS)

    Valint, P.L. Jr.

    1982-01-01

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

  15. U uranium. Suppl. Vol. D3

    International Nuclear Information System (INIS)

    Haug, H.O.

    1982-01-01

    This volume of the uranium series of the Gmelin handbook deals with the anion exchange of uranium. Compounds of the valence states of III, IV, V and VI of uranium in halide, nitrate, sulfate, phosphate, and carbonate media as well as in media containing organic complexing agents are treated. The literature cited covers the period from about 1947 to the end of 1980. (RB) [de

  16. Activation of chalcogens and chalcogenides at reactive uranium centers

    Energy Technology Data Exchange (ETDEWEB)

    Franke, Michael Sebastian

    2015-07-23

    -κ{sup 1}:κ{sup 2}-COSE)] (E = S, Se) could be obtained via insertion of CO{sub 2} or COS into the U-E bond, whereas CS{sub 2} is added to the U-Se-U bond and thus forms dithioselenocarbonate [{(("A"d","M"eArO)_3N)U"I"V(DME)}{sub 2}(μ-κ{sup 2}:κ{sup 2}-CS{sub 2}Se)]. The synthesis of terminal uranium monochalcogenido complexes with a U=E multiple bond is of great current interest, as ligands containing soft donor atoms such as sulfur, selenium, and tellurium are expected to participate in covalent bonding with uranium.s 5f-orbitals. Generating those compounds is difficult due to the high nucleophilicity of the E{sup 2-} ligands and requires special conditions to prevent the formation of di-, tri-, and polynuclear species. The development of new precursor complexes in order to access terminal uranium monochalcogenido species was another subject of this thesis and resulted in the synthesis of the hydrochalcogenido complexes [(({sup Ad,Me}ArO){sub 3}N)U{sup IV}(DME)(EH)] from H{sub 2}E (E = S, Se, Te). Many terminal ligands like the nitrido (N{sup 3-}), phosphido (P{sup 3-}), and chalcogenido (O{sup 2-}, S{sup 2-}, Se{sup 2-}, Te{sup 2-}) moieties are very reactive and require metal complexes with sterically demanding, supporting ligands that prevent undesired further reactivity. As a consequence, a new phenol HOAr* (Ar* = 2,6-(CHPh{sub 2}){sub 2}-4-Me-C{sub 6}H{sub 2}, 2,6-bis(diphenylmethyl)-4-methylphenyl) that combines bulkiness around the uranium center with very high flexibility, was developed to be used for uranium coordination chemistry. Depending on the reaction conditions, both a THF-coordinated and a solvent-free uranium(III) tris(aryloxo) complex could be obtained. Both compounds exhibit a uranium-(η{sup 6}-arene) interaction in their respective molecular structures, which could be further confirmed through DFT calculations. In a preliminary reactivity study it is shown that both uranium(III) complexes, the THF-coordinated and the coordinatively unsaturated

  17. The primary discuss with migmatite uranium mineralization of 505 uranium points in Datian, Panzhihua, Sichuan province

    International Nuclear Information System (INIS)

    Zhao Jianbo; Yao Jian; Li Pilin

    2012-01-01

    The Presinian migmatitic complexes of Kangding Group distributed along 505 area of Datian, Panzhihua, Sichuan Province. Describing the geological features on 505 Uranium points, summarizing and analyzing the genesis of the migmatite complexes, overall structure, hydrothermal alteration, ore characteristics. It comes to a conclusion that the mineral type is migmatite uranium mineralization which is controlled by the migmatization and east-west structure. (authors)

  18. Uranium update

    International Nuclear Information System (INIS)

    Steane, R.

    1997-01-01

    This paper is about the current uranium mining situation, especially that in Saskatchewan. Canada has a unique advantage with the Saskatchewan uranium deposits. Making the most of this opportunity is important to Canada. The following is reviewed: project development and the time and capital it takes to bring a new project into production; the supply and demand situation to show where the future production fits into the world market; and our foreign competition and how we have to be careful not to lose our opportunity. (author)

  19. Oxidation of uranium and uranium alloys

    International Nuclear Information System (INIS)

    Orman, S.

    1976-01-01

    The corrosion behaviour of uranium in oxygen, water and water + oxygen mixtures is compared and contrasted. A considerable amount of work, much of it conflicting, has been published on the U + H 2 O and U + H 2 O + O 2 systems. An attempt has been made to summarise this data and to explain the reasons for the lack of agreement between the experimental results. The evidence for the mechanism involving OH - ion diffusion as the reacting entity in both the U + H 2 O and U + O 2 + H 2 O reactions is advanced. The more limited corrosion data on some lean uranium alloys and on some higher addition alloys referred to as stainless materials is summarised together with some previously unreported results obtained with these materials at AWRE. The data indicates that in the absence of oxygen the lean alloys behave in a similar manner to uranium and evolve hydrogen in approximately theoretical quantities. But the stainless alloys absorb most of the product hydrogen and assessments of reactivity based on hydrogen evolution would be very inaccurate. The direction that future corrosion work on these materials should take is recommended

  20. Efficient blue-green and green electroluminescent devices obtained by doping iridium complexes into hole-block material as supplementary light-emitting layer

    Energy Technology Data Exchange (ETDEWEB)

    Zhou, Liang [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Zheng, Youxuan, E-mail: yxzheng@mail.nju.edu.cn [State Key Laboratory of Coordination Chemistry, Nanjing National Laboratory of Microstructures, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093 (China); Deng, Ruiping; Feng, Jing; Song, Mingxing; Hao, Zhaomin [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Zhang, Hongjie, E-mail: hongjie@ciac.jl.cn [State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China); Zuo, Jinglin; You, Xiaozeng [State Key Laboratory of Coordination Chemistry, Nanjing National Laboratory of Microstructures, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093 (China)

    2014-04-15

    In this work, organic electroluminescent (EL) devices with dominant and supplementary light-emitting layers (EMLs) were designed to further improve the EL performances of two iridium{sup III}-based phosphorescent complexes, which have been reported to provide EL devices with slow EL efficiency roll-off. The widely used hole-block material 2,2′,2''-(1,3,5-Benzinetriyl)-tris(1-phenyl-1-H-benzimidazole) (TPBi) was selected as host material to construct the supplementary EML. Compared with single-EML devices, double-EMLs devices showed higher EL efficiencies, higher brightness, and lower operation voltage attributed to wider recombination zone and better balance of carriers. In addition, the insertion of supplementary EML is instrumental in facilitating carriers trapping, thus improving the color purity. Finally, high performance blue-green and green EL devices with maximum current efficiencies of 35.22 and 90.68 cd/A, maximum power efficiencies of 26.36 and 98.18 lm/W, and maximum brightness of 56,678 and 112,352 cd/m{sup 2}, respectively, were obtained by optimizing the doping concentrations. Such a device design strategy extends the application of a double EML device structure and provides a chance to simplify device fabrication processes. -- Highlights: • Electroluminescent devices with supplementary light-emitting layer were fabricated. • Doping concentrations and thicknesses were optimized. • Better balance of holes and electrons causes the enhanced efficiency. • Improved carrier trapping suppresses the emission of host material.

  1. Autonomic components of Complex Regional Pain Syndrome (CRPS) are favourably affected by Electrical Twitch-Obtaining Intramuscular Stimulation (ETOIMS): effects on blood pressure and heart rate.

    Science.gov (United States)

    Chu, Jennifer; Bruyninckx, Frans; Neuhauser, Duncan V

    2017-07-01

    Favourable pain relief results on evoking autonomous twitches at myofascial trigger points with Electrical Twitch Obtaining Intramuscular Stimulation (ETOIMS). To document autonomic nervous system (ANS) dysfunction in Complex Regional Pain Syndrome (CRPS) from blood pressure (BP) and pulse/heart rate changes with ETOIMS. A patient with persistent pain regularly received serial ETOIMS sessions of 60, 90, 120 or ≥150 min over 24 months. Outcome measures include BP: systolic, diastolic, pulse pressure and pulse/heart rate, pre-session/immediate-post-session summed differences (SDPPP index), and pain reduction. His results were compared with that of two other patients and one normal control. Each individual represented the following maximal elicitable twitch forces (TWF) graded 1-5: maximum TWF2: control subject; maximum TWF3: CRPS patient with suspected ANS dysfunction; and maximum TWF4 and TWF5: two patients with respective slow-fatigue and fast-fatigue twitches who during ETOIMS had autonomous twitching at local and remote myotomes simultaneously from denervation supersensitivity. ETOIMS results between TWFs were compared using one-way analysis of variance test. The patients showed immediate significant pain reduction, BP and pulse/heart rate changes/reduction(s) except for diastolic BP in the TWF5 patient. TWF2 control subject had diastolic BP reduction with ETOIMS but not with rest. Linear regression showed TWF grade to be the most significant variable in pain reduction, more so than the number of treatments, session duration and treatment interval. TWF grade was the most important variable in significantly reducing outcome measures, especially pulse/heart rate. Unlike others, the TWF3 patient had distinctive reductions in SDPPP index. Measuring BP and pulse/heart rate is clinically practical for alerting ANS dysfunction maintained CRPS. SDPPP index (≥26) and pulse/heart rate (≥8) reductions with almost every ETOIMS treatment, plus inability to evoke

  2. Machining of uranium and uranium alloys

    International Nuclear Information System (INIS)

    Morris, T.O.

    1981-01-01

    Uranium and uranium alloys can be readily machined by conventional methods in the standard machine shop when proper safety and operating techniques are used. Material properties that affect machining processes and recommended machining parameters are discussed. Safety procedures and precautions necessary in machining uranium and uranium alloys are also covered. 30 figures

  3. Training manual for uranium mill workers on health protection from uranium

    International Nuclear Information System (INIS)

    McElroy, N.; Brodsky, A.

    1986-01-01

    This report provides information for uranium mill workers to help them understand the radiation safety aspects of working with uranium as it is processed from ore to yellowcake at the mills. The report is designed to supplement the radiation safety training provided by uranium mills to their workers. It is written in an easily readable style so that new employees with no previous experience working with uranium or radiation can obtain a basic understanding of the nature of radiation and the particular safety requirements of working with uranium. The report should be helpful to mill operators by providing training material to support their radiation safety training programs

  4. Linear uranium complexes X2UL5 with L=cyanide, iso-cyanate: DFT evidence for similarities between uranyl (X = O) and uranocene (X = Cp) derivatives

    International Nuclear Information System (INIS)

    Iche-Tarrat, N.; Marsden, Colin J.; Barros, N.; Maron, L.; Barros, N.

    2008-01-01

    A DFT study of the isostructural compounds [UO 2 L 5 ] n- with n=3-5 and linear [Cp 2 UL 5 ] m- with m=1-3 has been carried out for two different anionic ligands. Structurally stable structures are obtained for all systems. The coordination competition between cyanide (CN - ) and isocyanide (NC - ) as well as between cyanate (OCN - ) and iso-cyanate (NCO - ) has been studied in the uranyl case. A clear preference for cyanide and iso-cyanate complexes is reported. The coordination of five ligands in the equatorial plane is rationalized by the analysis of the MO diagram of both systems. Moreover, the qualitative comparison of the two MO diagrams shows a high similarity in agreement with the isolobality concept. The existence of linear [Cp 2 UL 5 ] - organometallic U(VI) complexes is thus proposed, as well as the possibility of obtaining complexes of both types for U(VI) and U(V) with OCN - ligands. In addition, the U(IV) linear metallocene is calculated to be stable for the latter ligand. (authors)

  5. The peraluminous leucogranitic complex of St Sylvestre (France, Massif Central NW). Evolution of the crystallochemistry of mineral phases and of the geochemistry of major and trace elements. Polygenetism characterization in peraluminous granites. Implication on uranium metallogeny

    International Nuclear Information System (INIS)

    Friedrich, M.

    1983-07-01

    The main purpose of this study is to improve the knowledge of the behaviour of uranium during magmatic and late magmatic processes. In France and other part of the world the close association of uranium (Sn-W) deposits and showings with this type of granite justifies the metallogenic interest of this study. At the scale of the whole granitic complex two distinct petrological groups are redefined: the facies of Brame and St Sylvestre. Mineral paragenesis closely follow the geochemical differentiation. Abundance of uraninite and scarcity of monazite and zircon, are additional features of these samples. The opposite behaviour of monazite (typical of the less evolved facies) and uraninite (whose abundance is directly related to the degree of differentiation) suggests two conclusions. Abundance in uranium is directly related to the magmatic differentiation processes. The early crystallization of monazite and zircon and their high abundance in poorly evolved facies imply a compatible behaviour for Th, Zr and light rare earths. More detailed geochemical studies evidence heterogeneities at on hectometric and locally at a metric scale. Differentiation processes, which appear to be continuous at a kilometric scale in the St Sylvestre facies, are discontinuous at the hectometric and metric scale. Such petrogeochemical discontinuities, implying petrogenitic heterogeneities are expressed in the concept of polygenetism [fr

  6. Uranium fluorides analysis. Titanium spectrophotometric determination

    International Nuclear Information System (INIS)

    Anon.

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

  7. Differential pulse cathodic stripping voltammetric determination of uranium with arsenazo-III at the hanging mercury dropping electrode

    Energy Technology Data Exchange (ETDEWEB)

    Kadi, M.W.; El-Shahawi, M.S. [Chemistry Dept., King Abdulaziz Univ., Jeddah (Saudi Arabia)

    2009-07-01

    An accurate, inexpensive and less laborious controlled adsorptive accumulation of uranium(VI)-arsenazo-III on a hanging mercury drop electrode (HMDE) has been developed for uranium(VI) determination. The method is based upon the collection of uranium(VI)-arsenazo-III complex at pH 5-6 at the HMDE and subsequent direct stripping measurement of the element in the nanomolar concentration level. The cathodic peak current (i{sub p,c}) of the adsorbed complex ions of uranium(VI) was measured at -0.35 V vs. Ag/AgCl reference electrode by differential pulse cathodic stripping voltammetry (DP-CSV), proceeded by an accumulation period of 150s2.5 in Britton-Robinson buffer of pH 5. The plot of the resulting i{sub p,c} vs. uranium(VI) concentration was linear in the range 2.1 x 10{sup -9} to 9.60 x 10{sup -7} mol L{sup -1} uranium(VI) and tended to level off at above 9.6 x 10{sup -7} mol L{sup -1}. The limits of detection and quantification of uranium(VI) were found to be 4.7 x 10{sup -10} and 1.5 x 10{sup -9} mol L{sup -1}, respectively. A relative standard deviation of {+-}2.39% (n = 5) at 8.5 x 10{sup -7} mol L{sup -1} uranium(VI) was obtained. The method was validated by comparing the results with that obtained by ICP-MS method with RSD less than {+-}3.3%. The method was applied successfully for the analysis of uranium in certified reference material (IAEA soil-7), and in phosphate fertilizers. (orig.)

  8. Investigation of adsorbers for the extracting of uranium from seawater

    International Nuclear Information System (INIS)

    Witte, E.G.; Astheimer, L.; Schenk, H.J.; Schwochau, K.

    1979-01-01

    Organic ion exchangers have been tested with respect to their efficiency uranium from seawater. A complexing polymer resin which combines fast uptake of uranium with high selectivity is found to be able to accumulate uranium from natural seawater by a factor of 2.6 x 10 5 . (orig.) 891 HK/orig. 892 MKO [de

  9. Uranium industry annual 1996

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-04-01

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

  10. Uranium industry annual 1996

    International Nuclear Information System (INIS)

    1997-04-01

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

  11. Assessment of the uranium potential of the Jurassic volcanism (Bahía Laura and El Quemado Complexes), Province of Santa Cruz, using ground-borne gamma-ray spectrometry and rock geochemistry

    International Nuclear Information System (INIS)

    Kleinman, L.E.; Maloberti, A.L.; Gayone, M.R.; Kaufmann, C.; Sruoga, P.

    2013-01-01

    Radiometric surveys are a rapid tool to measure uranium (U), thorium (Th) and potassium (K) concentrations in rocks and are very useful in the exploration for radioactive minerals. The distribution of uranium in Jurassic volcanic rocks of the province of Santa Cruz is evaluated in this work using ground gamma-ray spectrometry and rock geochemistry in order to assess its potential to form uranium deposits. Five areas were selected, which had some previous data of high radiometric values and detailed geological information. Measurements were carried out with a portable gamma-ray spectrometer (Exploranium-GR 320®) in andesites, ignimbrites, rhyolites, silicified areas, ash-fall tuffs and lacustrine sediments corresponding to the Bahía Laura and to El Quemado complexes. The results were similar in the five surveyed areas: radiometric concentrations show good positive correlations with chemical composition of the studied rocks for both K and Th, and a relatively poorer correlation for U. Different processes such as magmatic differentiation, vapor phase crystallization, hydrothermal alteration and supergene alteration are reflected in the distribution of these elements. U concentrations increase in the more glassy rocks, in areas with hydrothermal silicification, and in fracture zones, features that should be considered in future surveys. The calkalkaline composition and arc-signatures of the Jurassic magmatism are not the most favorable for uranium enrichment and for concentration of significant mineralizations. However, the extensional tectonic setting; the occurrence of calderas with facies slightly enriched in U and Th, in addition to hydrothermal activity are positive factors for U exploration. (authors) [es

  12. Uranium industry annual, 1991

    International Nuclear Information System (INIS)

    1992-10-01

    In the Uranium Industry Annual 1991, 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. A feature article entitled ''The Uranium Industry of the Commonwealth of Independent States'' is included in this report

  13. Uranium refining by solvent extraction

    International Nuclear Information System (INIS)

    Kraikaew, J.; Srinuttrakul, W.

    2014-01-01

    The solvent extraction process to produce higher purity uranium from yellowcake was studied in laboratory scale. Yellowcake, which the uranium purity is around 70% and the main impurity is thorium, was obtained from monazite processing pilot plant of Rare Earth Research and Development Center in Thailand. For uranium re-extraction process, the extractant chosen was Tributylphosphate (TBP) in kerosene. It was found that the optimum concentration of TBP was 10% in kerosene and the optimum nitric acid concentration in uranyl nitrate feed solution was 4 N. An increase in concentrations of uranium and thorium in feed solution resulted in a decrease in the distribution of both components in the extractant. However, the distribution of uranium into the extractant was found to be more than that of thorium. The equilibration study of the extraction system, UO_2(NO_3)/4N HNO_3 – 10%TBP/Kerosene, was also investigated. Two extraction stages were calculated graphically from 100,000 ppm uranium concentration in feed solution input with 90% extraction efficiency and the flow ratio of aqueous phase to organic phase was adjusted to 1.0. For thorium impurity scrubbing process, 10% TBP in kerosene was loaded with uranium and minor thorium from uranyl nitrate solution prepared from yellowcake and was scrubbed with different low concentration nitric acid. The results showed that at nitric acid normality was lower than 1 N, uranium distributed well to aqueous phase. As conclusion, optimum nitric acid concentration for scrubbing process should not less than 1 N and diluted nitric acid or de-ionized water should be applied to strip uranium from organic phase in the final refining process. (author)

  14. Oxidation-extraction of uranium from wet-process phosphoric acid

    International Nuclear Information System (INIS)

    Lawes, B.C.

    1985-01-01

    The invention involves an improvement to the reductive stripping process for recovering uranium values from wet-process phosphoric acid solution, where uranium in the solution is oxidized to uranium (VI) oxidation state and then extracted from the solution by contact with a water immiscible organic solvent, by adding sufficient oxidant, hydrogen peroxide, to obtain greater than 90 percent conversion of the uranium to the uranium (VI) oxidation state to the phosphoric acid solution and simultaneously extracting the uranium (VI)

  15. Case study of forecasting uranium supply and demand

    International Nuclear Information System (INIS)

    Noritake, Kazumitsu

    1992-01-01

    PNC collects and analyzes information about uranium market trend, world uranium supply and demand, and world uranium resources potential in order to establish the strategy of uranium exploration. This paper outlines the results obtained to forecast uranium supply and demand. Our forecast indicates that 8,500 tU, accounting for one-sixth of the demand in the year 2001, must be met by uranium produced by mines to be newly developed. After 2019, demand cannot be met by the 123 mines currently in operation or expected to have gone into production by this year. The projected shortage must therefore be covered by uranium to be newly discovered. To preclude this occurrence, uranium exploration will have to be steadily continued in order to ensure future new uranium resources, to alleviate anxiety about future supply, and to prevent sharp price hikes. (author)

  16. Potentiometric determination of uranium in the presence of plutonium in Hsub(2)SOsub(4) medium

    International Nuclear Information System (INIS)

    Gopinath, N.; Rama Rao, G.A.; Manchanda, V.K.; Natarajan, P.R.

    1985-01-01

    The potentiometric determination of uranium is widely carried out in phosphoric acid medium to suppress the interferences of plutonium by complexation. Owing to the complexity of the recycling plutonium from the phosphate based waste involving manifold stages of separation, a method is proposed which does not use phosphoric acid. Uranium and plutonium are reduced to U(IV) and Pu(III) in IM Hsub(2)SOsub(4) by Ti(III), and NaNOsub(2) is chosen to selectively oxidize Pu(III) and the excess of Ti(III). The unreacted NaNOsub(2) is destroyed by sulphamic acid and excess Fe(III) is added following dilution. The euqivalent amount of Fe(II) thus liberated is titrated against standard Ksub(2)Crsub(2)Osub(7). RSD obtained for the determination of uranium (1-2 mg) is 0.3% with plutonium present up to 4.0 mg. (author)

  17. A study on chlorination of uranium metal using ammonium chloride

    International Nuclear Information System (INIS)

    Eun, H.C.; Kim, T.J.; Jang, J.H.; Kim, G.Y.; Lee, S.J.; Hur, J.M.

    2017-01-01

    In this study, the chlorination of uranium metal using ammonium chloride (NH 4 Cl) was conducted to derive an easy and simple uranium chloride production method without impurities. In thermodynamic equilibrium calculations, it was predicted that only uranium chlorides can be produced by the reactions between uranium metal and NH 4 Cl. Experimental conditions for the chlorination of uranium metal were determined using a chlorination test of cerium metal using NH 4 Cl. It was confirmed that UCl 3 and UCl 4 in the form of particles as uranium chlorination products can be obtained from the chlorination method using NH 4 Cl. (author)

  18. Spectrophotometric determination of uranium with arsenazo previous liquid-liquid extraction and colour development in organic medium; Determinacion espectrofotometrica de uranio con arsenazo, previa extraccion y desarrollo del color en medio organico

    Energy Technology Data Exchange (ETDEWEB)

    Palomares Delgado, F; Vera Palomino, J; Petrement Eguiluz, J C

    1964-07-01

    The determination of uranium with arsenazo is hindered by a great number of cation which form stable complexes with the reactive and may given rise to serious interferences. By studying the optimum conditions of uranium the extraction be means of tributylphosphate solutions dissolved in methylisobuthylketone, under conditions for previous masking of the interfering cations, an organic extract was obtained containing all the uranium together with small amounts of iron. The possible interference derived from the latter element is avoided by reduction with hydroxylammoniumchlorid followed by complex formation of the Fe(II)-ortophenantroline compound in alcoholic medium. (Author) 17 refs.

  19. Paragenesis and Geochronology of the Nopal I Uranium Deposit, Mexico

    Energy Technology Data Exchange (ETDEWEB)

    M. Fayek; M. Ren

    2007-02-14

    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.

  20. An alternate procedure in the recovery of no fissioned remainder uranium in the production of molybdenum 99 from fission

    International Nuclear Information System (INIS)

    Acosta Chavez, A.L.

    1992-01-01

    An effective modification of the chemical processes to dissolve the U-IV in the dissolver has been obtained, using its highly alkaline pH and extracting it as Uranyl Triperoxidate soluble anionic complex, in its experimental design without fission products. Even when the extraction of uranium is usually more complete through acidic dissolution, the characteristics for the dissolver used in production of fission Mo-99 do not allow this kind of extraction and alkaline option is more adecuate for this purpose. The dissolution of the insoluble residue, through the production of the anionic Triperoxidate Uranyl complexes, arises rapidly due to the presence of and oxidizing agent. The best results in the extraction of soluble Uranium were obtained with and organic solvent and a mixture of carbonate/bicarbonate. The concentrated Uranium in the aqueous alkaline solution was separated through fixation as an anion Tricarbonate of Uranyl in columns of anionic resin, moderately basic in dynamic conditions. The superiority of the resin used, over other exchangers, was evident in the elution with nitric acid that may be done for small volumes with a quite favorable separation of Uranium. The eluate contains the Uranium as an hexahydrated Uranyl Nitrate with a high degree of purity in reduced volume, in an average concentration of 90.2 % with respect to the initial concentration of Uranium (Author)

  1. Uranium - what role

    International Nuclear Information System (INIS)

    Grey, T.; Gaul, J.; Crooks, P.; Robotham, R.

    1980-01-01

    Opposing viewpoints on the future role of uranium are presented. Topics covered include the Australian Government's uranium policy, the status of nuclear power around the world, Australia's role as a uranium exporter and problems facing the nuclear industry

  2. Brazilian uranium exploration program

    International Nuclear Information System (INIS)

    Marques, J.P.M.

    1981-01-01

    General information on Brazilian Uranium Exploration Program, are presented. The mineralization processes of uranium depoits are described and the economic power of Brazil uranium reserves is evaluated. (M.C.K.) [pt

  3. Uranium enrichment

    International Nuclear Information System (INIS)

    1991-11-01

    This paper analyzes under four different scenarios the adequacy of a $500 million annual deposit into a fund to pay for the cost of cleaning up the Department of Energy's (DOE) three aging uranium enrichment plants. These plants are located in Oak Ridge, Tennessee; Paducah, Kentucky; and Portsmouth, Ohio. In summary the following was found: A fixed annual $500 million deposit made into a cleanup fund would not be adequate to cover total expected cleanup costs, nor would it be adequate to cover expected decontamination and decommissioning (D and D) costs. A $500 million annual deposit indexed to an inflation rate would likely be adequate to pay for all expected cleanup costs, including D and D costs, remedial action, and depleted uranium costs

  4. Uranium production

    International Nuclear Information System (INIS)

    Spriggs, M.

    1980-01-01

    The balance between uranium supply and demand is examined. Should new resources become necessary, some unconventional sources which could be considered include low-grade extensions to conventional deposits, certain types of intrusive rock, tuffs, and lake and sea-bed sediments. In addition there are large but very low grade deposits in carbonaceous shales, granites, and seawater. The possibility of recovery is discussed. Programmes of research into the feasibility of extraction of uranium from seawater, as a by-product from phosphoric acid production, and from copper leach solutions, are briefly discussed. Other possible sources are coal, old mine dumps and tailings, the latter being successfully exploited commercially in South Africa. The greatest constraints on increased development of U from lower grade sources are economics and environmental impact. It is concluded that apart from U as a by-product from phosphate, other sources are unlikely to contribute much to world requirements in the foreseeable future. (U.K.)

  5. 77 FR 73056 - Application for a License To Export High-Enriched Uranium

    Science.gov (United States)

    2012-12-07

    ... NUCLEAR REGULATORY COMMISSION Application for a License To Export High-Enriched Uranium Pursuant... Complex. Uranium (93.2%). uranium-235 at CERCA AREVA Romans October 10, 2012 contained in 6.2 in France and to October 12, 2012 kilograms irradiate targets at XSNM3729 uranium. the BR-2 Research 11006053...

  6. 77 FR 73055 - Application for a License To Export High-Enriched Uranium

    Science.gov (United States)

    2012-12-07

    ... NUCLEAR REGULATORY COMMISSION Application for a License To Export High-Enriched Uranium Pursuant.... Security Complex. Uranium uranium-235 at CERCA AREVA October 10, 2012 (93.35%). contained in Romans in France October 12, 2012 10.1 kilograms and to irradiate XSNM3730 uranium. targets at the HFR 11006054...

  7. 78 FR 33448 - Application for a License To Export High-Enriched Uranium

    Science.gov (United States)

    2013-06-04

    ... NUCLEAR REGULATORY COMMISSION Application for a License To Export High-Enriched Uranium Pursuant.... Security Complex, May 13, Uranium (93.35%). uranium-235 at the National 2013, May 21, 2013, XSNM3745, contained in 7.5 Research Universal 11006098. kilograms reactor in Canada for uranium. ultimate use in...

  8. 76 FR 72984 - Revised Application for a License To Export High-Enriched Uranium

    Science.gov (United States)

    2011-11-28

    ... NUCLEAR REGULATORY COMMISSION Revised Application for a License To Export High-Enriched Uranium The application for a license to export high-enriched Uranium has been revised as noted below. Notice... fabricate fuel France. Security Complex; October 18, Uranium (93.35%). uranium (174.0 elements in France...

  9. Influence of acidified acidity to uranium bioleaching

    International Nuclear Information System (INIS)

    Li Jiang; Liu Yajie; Zheng Zhihong; Yuan Baohua; Shen Chuan; Shi Weijun

    2012-01-01

    The relationship between the acidified acidity and the acid consumption and uranium leaching rate in the process of uranium bioleaching is investigated. Results indicate that higher uranium leaching rate is obtained when the relatively high acidity was applied at beginning. For different minerals, although the original acidity should be different, lower original acidity was not better for shortening leaching period and improving uranium leaching rate. It confirms 30-40 g/L sulfuric acid as the original acidity was more suitable and more than 30 g/ L should be applied if the mineral particle sizes were larger. (authors)

  10. Titrimetric determination of uranium in tributyl phosphate

    International Nuclear Information System (INIS)

    Sobkowska, A.

    1978-01-01

    The titrimetric method involving the reduction of U(VI) to uranium(IV) by iron(II) in phosphoric acid, selective oxidation of the excess of iron(II) and potentiometric titration with dichromate was directly used for the determination of uranium in tributyl phosphate mixtures. The procedure was applied to solutions containing more than 2 mg of uranium in the sample but the highest precision and accuracy were obtained in the range from 20 to 200 mg of uranium. Dibutyl phosphate and monobutyl phosphate as well as the other radiolysis products of TBP had no influence on the results of determinations. (author)

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

    International Nuclear Information System (INIS)

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

    1992-01-01

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

  12. Uranium enrichment

    International Nuclear Information System (INIS)

    1991-08-01

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

  13. Uranium Metal Analysis via Selective Dissolution

    Energy Technology Data Exchange (ETDEWEB)

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

    2008-09-10

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

  14. Drawing of uranium in γ phase

    International Nuclear Information System (INIS)

    Stohr, J.A.

    1955-01-01

    It describes the study of working and drawing of uranium in γ phase. In a first part, the forgeable characteristics of uranium metal in the three different phases (α, β and γ) are compared by using BASTIEN-PORTEVIN method. The different experiments are testing the behaviour metal in each phase under different stresses and a temperature gradient as slow and shock traction, slow and shock compression, resilience, flexibility. Results show that optimum conditions for uranium drawing is uranium in phase γ. In a second part, it described the drawing method and process. The uranium rods obtained by this technique are of very good quality. In addition, the material wear is very low which permits a low production cost. Finally, the uranium rod physical properties are studied. (M.P.)

  15. Derived enriched uranium market

    International Nuclear Information System (INIS)

    Rutkowski, E.

    1996-01-01

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

  16. On the uptake and binding of uranium (VI) by the green alga Chlorella Vulgaris

    International Nuclear Information System (INIS)

    Vogel, Manja

    2011-01-01

    the algae cells during the sorption experiment and a behavior analogue to initially heat killed cells. Differences in the contribution of functional groups to the uranium binding depending on the metabolic activity of the algal biomass were also shown by the difference spectra of the ATR-FTIR measurements calculated between uranium contaminated and untreated biomass. All together the spectroscopic investigations showed in case of Chlorella vulgaris a mixture of functional groups is responsible for the coordination of U(VI). The metabolic activity of the cells influences the binding of uranium under the given experimental conditions. Models of the structure of the formed U(VI)-algae complexes in dependence of the metabolic activity were created. For living algal cells, mainly carboxylic and organic phosphate groups are involved in the binding of uranium, whereas in dead algal biomass additionally inorganic phosphates are involved to some extend in the interaction of uranium with algal cells. The transferability of the obtained findings concerning the experiments in mineral medium to natural occurring mining related waters was verified exemplary with the surface water of ''Gessenwiese'' (former ''Gessenhalde'' at Ronneburg). The obtained results of this study contribute to the prediction of the migration behavior of uranium under environmental conditions, the radiological risk assessment of geogenic and anthropogenic appearing uranium and a reliable estimation of the accumulation of uranium in the food chain.

  17. Hydrolysis of uranium monocarbide

    International Nuclear Information System (INIS)

    Hajek, B.; Karen, P.; Brozek, V.

    1984-01-01

    The substoichiometric uranium monocarbide UCsub(0.95) was hydrolyzed in acid medium at 80 degC. The composition of the products of hydrolysis corresponds to published data but it correlates better with the stoichiometric composition of the hydrolyzable carbide. The mechanisms of the hydrolytic reaction are discussed and a modified radical mechanism is suggested based on the concept of initiation of the radical process by Hsup(.) radicals formed owing to the nonstoichiometry of the substance. A relation is proposed for calculating the content of free hydrogen in the hydrolysis products of carbides of metallic nature for which a radical mechanism of their reaction with water can be assumed. Some effects occurring during the hydrolysis of uranium carbide, as described in literature, are explained in terms of the concept suggested. The results obtained by the authors for carbides of manganese (Mn 7 C 3 ) and for rare earth elements are discussed. (author)

  18. Processing of Sierra Albarrana uranium ores

    International Nuclear Information System (INIS)

    Gutierrez Jodra, L.; Perez Luina, A.; Perarnau, M.

    1960-01-01

    Uranium recovery by hydrometallurgy from brannerite, found in Hornachuelos (Cordoba) is described. It has been studied the acid and alkaline leaching and salt roasting, proving as more satisfactory the acid leaching. Besides the uranium solubilization by acid leaching, is described the further process to obtain pure uranyl nitrate. (Author)

  19. A spectroscopic study of uranium(VI) interaction with magnetite

    International Nuclear Information System (INIS)

    El Aamrani, S.; Gimenez, J.; Rovira, M.; Seco, F.; Grive, M.; Bruno, J.; Duro, L.; Pablo, J. de

    2007-01-01

    The uranium sorbed onto commercial magnetite has been characterized by using two different spectroscopic techniques such as X-ray photoelectron spectroscopy (XPS), and extended X-ray absorption fine structure (EXAFS). Magnetite samples have been put in contact with uranium(VI) solutions in conditions in which a high uranium uptake is expected. After several days, the magnetite surface has been analysed by XPS and EXAFS. The XPS results obtained are not conclusive regarding the uranium oxidation state in the magnetite surface. On the other hand, the results obtained with the EXAFS technique show that the uranium-magnetite sample spectrum has characteristics from both the UO 2 and schoepite spectra, e.g. a relatively high coordination number of equatorial oxygens and two axial oxygens, respectively. These results would indicate that the uranium sorbed onto magnetite would be a mixture of uranium(IV) and uranium(VI)

  20. Uranium manufacturing process employing the electrolytic reduction method

    International Nuclear Information System (INIS)

    Oda, Yoshio; Kazuhare, Manabu; Morimoto, Takeshi.

    1986-01-01

    The present invention related to a uranium manufacturing process that employs the electrolytic reduction method, but particularly to a uranium manufacturing process that employs an electrolytic reduction method requiring low voltage. The process, in which uranium is obtained by means of the electrolytic method and with uranyl acid as the raw material, is prior art

  1. Uranium industry annual, 1986

    International Nuclear Information System (INIS)

    1987-01-01

    Uranium industry data collected in the EIA-858 survey provide a comprehensive statistical characterization of annual activities of the industry and include some information about industry plans over the next several years. This report consists of two major sections. The first addresses uranium raw materials activities and covers the following topics: exploration activities and expenditures, resources and reserves, mine production of uranium, production of uranium concentrate, and industry employment. The second major section is concerned with the following uranium marketing activities: uranium purchase commitments, uranium prices, procurement arrangements, uranium imports and exports, enrichment services, inventories, secondary market activities utility market requirements and related topics

  2. Uranium Industry. Annual 1984

    International Nuclear Information System (INIS)

    Lawrence, M.S.S.

    1985-01-01

    This report provides a statistical description of activities of the US uranium industry during 1984 and includes a statistical profile of the status of the industry at the end of 1984. It is based on the results of an Energy Information Administration (EIA) survey entitled ''Uranium Industry Annual Survey'' (Form EIA-858). The principal findings of the survey are summarized under two headings - Uranium Raw Materials Activities and Uranium Marketing Activities. The first heading covers exploration and development, uranium resources, mine and mill production, and employment. The second heading covers uranium deliveries and delivery commitments, uranium prices, foreign trade in uranium, inventories, and other marketing activities. 32 figs., 48 tabs

  3. Uranium. Suppl. Vol. C7

    International Nuclear Information System (INIS)

    Keim, R.; Keller, C.

    1982-01-01

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

  4. Aftermath of Uranium Ore Processing on Floodplains: Lasting Effects of Uranium on Soil and Microbes

    Science.gov (United States)

    Tang, H.; Boye, K.; Bargar, J.; Fendorf, S. E.

    2016-12-01

    A former uranium ore processing site located between the Wind River and the Little Wind River near the city of Riverton, Wyoming, has generated a uranium plume in the groundwater within the floodplain. Uranium is toxic and poses a threat to human health. Thus, controlling and containing the spread of uranium will benefit the human population. The primary source of uranium was removed from the processing site, but a uranium plume still exists in the groundwater. Uranium in its reduced form is relatively insoluble in water and therefore is retained in organic rich, anoxic layers in the subsurface. However, with the aid of microbes uranium becomes soluble in water which could expose people and the environment to this toxin, if it enters the groundwater and ultimately the river. In order to better understand the mechanisms controlling uranium behavior in the floodplains, we examined sediments from three sediment cores (soil surface to aquifer). We determined the soil elemental concentrations and measured microbial activity through the use of several instruments (e.g. Elemental Analyzer, X-ray Fluorescence, MicroResp System). Through the data collected, we aim to obtain a better understanding of how the interaction of geochemical factors and microbial metabolism affect uranium mobility. This knowledge will inform models used to predict uranium behavior in response to land use or climate change in floodplain environments.

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

    International Nuclear Information System (INIS)

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

    2008-01-01

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

  6. Near field chemical speciation: the reaction of uranium and thorium with Hanford basalt and elevated pH

    International Nuclear Information System (INIS)

    Perry, D.L.

    1984-01-01

    The hydrolysis of radionuclides such as thorium and uranium and their subsequent chemisorption on Hanford basalt have been studied using a variety of techniques, including x-ray photoelectron and infrared spectroscopy. Data obtained to date indicate mixed complexes of uranium and thorium to be on the basalt surface, the complexes being radionuclide oxides, hydrated oxides (hydroxides), and carbonates. These findings are discussed with respect to their importance for input for models describing speciation and dissolution processes involving nuclear waste repository materials such as Hanford basalt. 5 figures, 2 tables

  7. Uranium determination in different compositions

    International Nuclear Information System (INIS)

    Bulyanitsa, L.S.; Ivanova, K.S.; Ryzhinskij, M.V.; Alekseeva, N.A.; Solntseva, L.F.; Shereshevskaya, I.I.

    1978-01-01

    For clarifying the suitability of two different methods of analysis for determining uranium without its previous purification, the analysis of uranium carbides (UC, UC 2 , UC - ZrC) and alloys (U - Al, U - Zr - Nb, U- Ti) has been carried out. Dissolution of the compositions examined was carried out either after previous calcining (UC, UC 2 ) or fusion with KHSO 4 (UC - ZrC), or in phosphoric acid (alloys). The first method, a variant of potentiometric titration, has been modified for small amounts of uranium. Titration was carried out on a semiautomatic titrating unit. The uranium amount per titration is about 4 to 5 mg. The second method of analysis is the coulombmetric titration at a constant current intensity. The quantity of uranium per titration was equal to 1 - 3 mg. The statistical processing of the results obtained was carried out by a dispersion analysis that allowed to reveal the influence of separate factors, such as method of analysis, type of composition, the non-uniformity of a sample, the enumerated factors influencing the dispersion of the analysis results. It has been shown that the both methods are equally suitable for analysis of the uranium compounds examined

  8. Uranium - resources development and availability

    International Nuclear Information System (INIS)

    1983-01-01

    Australia possesses a major portion of the world's low cost uranium and it is confidently expected that further exploration will delineate yet more reserves. The level of such exploration and the rate of development of new production will remain critically dependent on world market developments. For the foreseeable future all development will be dedicated to supplying the export market. Australian government policies for uranium take account of both domestic and international concerns. With Australia, the policies act to protect the interests of the Aboriginal people affected by uranium production. In response to national interests and concerns, foreign investment in uranium production ventures is regulated in a manner which requires Australian control but allows a measure of foreign equity. Environmental concerns are recognized and projects may only be approved after comprehensive environmental protection procedures have been complied with. Without these policies public acceptability, which provides the foundations for long-term stability of the industry, would be prejudiced. On the world scene, Australia's safeguards policy serves to support international nuclear safeguards and, in particular, to honour its obligations under the Nuclear Non-Proliferation Treaty. Export policy requires that reasonable sales contract conditions apply and that fair negotiated market prices are obtained for Australia's uranium. Australia's recent re-emergence as a major producer and exporter of uranium is convincing testimony to the success of these policies. (author)

  9. A study on the formation of uranium carbide in an induction furnace

    International Nuclear Information System (INIS)

    Song, In Young; Lee, Yoon Sang; Kim, Eung Soo; Lee, Don Bae; Kim, Chang Kyu

    2005-01-01

    Uranium is a typical carbide-forming element. Three carbides, UC, U 2 C 3 and UC 2 , are formed in the uranium-carbon system. The most important of these as fuel is uranium monocarbide UC. It is well known that Uranium carbides can be obtained by three basic methods: 1) by reaction of uranium metal with carbon; 2) by reaction of uranium metal powder with gaseous hydrocarbons; 3) by reaction of uranium oxides with carbon. The use of uranium monocarbide, or materials based on it, has great prospects as fuel for nuclear reactors. It is quite possible that uranium dicarbide UC 2 may also acquire great importance as a fuel, particularly in dispersion fuel elements with graphite matrix. In the present study, uranium carbides are obtained by direct reaction of uranium metal with graphite in a high frequency induction furnace

  10. Contribution of analytical techniques coupled to the knowledge of the uranium speciation in natural conditions

    International Nuclear Information System (INIS)

    Petit, J.

    2009-06-01

    To understand the transport mechanisms and the radionuclides behaviour in the bio-geosphere is necessary to evaluate healthy and environmental risks of nuclear industry. These mechanisms are monitored by radioelements speciation, namely the distribution between their different physico-chemical forms in the environment. From this perspective, this PhD thesis deals with uranium speciation in a natural background. A detailed summary of uranium biogeochemistry has been written, which enables to restrict the PhD issue to uranium complexation with oxalic acid, a hydrophilic organic acid with good binding properties, ubiquitous in soil waters. Analytical conditions have been established by means of speciation diagrams. The speciation diagrams building by means of literature stability constants has allowed to define the analytical conditions of complex formation. The chosen analytical technique is the hyphenation of a separative technique (liquid chromatography LC or capillary electrophoresis CE) with mass spectrometry (ICPMS). The studied complexes presence in the synthetic samples has been confirmed with UV/visible spectrophotometry. LC-ICPMS analyses have proved the lability of the uranyl-organic acid complexes, namely their tendency to dissociate during analysis, which prevents from studying uranium speciation. CE-ICPMS study of labile complexes from a metal-ligand system has been made possible by employing affinity capillary electrophoresis, which enables to determine stability constants and electrophoretic mobilities. This PhD thesis has allowed to compare the different mathematical treatments of binding isotherm and to take into account ionic strength and real ligand concentration. Affinity CE has been applied successfully to lanthanum-oxalate (model system) and uranium-oxalate systems. The obtained results have been applied to a real system (situated in Le Bouchet). This shows the contribution of the developed method to the modelling of uranium speciation. (author)

  11. Direct separation of uranium and thorium from Qatrani phosphatic raw ore by consecutive percolation leaching

    Energy Technology Data Exchange (ETDEWEB)

    Hussein El-Sayed, M

    1984-07-01

    Phosphatic sandstone of Qatrani area contains high concentrations of uranium and thorium (1450 and 870 ppm respectively). These elements were directly separated from a representative sample of the ore by percolation leaching. Separation made was carried out by using two different leaching reagents, citric and nitric acids for obtaining two separate concentrates of U and Th consecutively from the sample. Uranium was leached first by using citric acid where other rock ingredients were left intact. The effects of: (a) increasing acid input amounts and (b) increasing leaching solution volumes (dilution) on U leaching efficiency were studied. The results revealed that citric acid reaction upon phosphate is limited in spite of higher residual acidity reported in the leach liquors. Regarding uranium, its leaching efficiency increased by increasing acid amounts and/or leaching solution volumes while fixing the acid input amounts. The efficiency of U leaching is more pronounced in the second case than in the first. Increasing U leaching while phosphate dissolution is limited could be interpreted as that the relative complexing affinity of citrate anion for hexavalent uranium is by far much greater than with phosphate. Thorium was thereafter leached by using dilute solutions of nitric acid to avoid dissolution of nitric acid to avoid dissolution of impurities. Percolation leaching experiments were thus performed on the uranium-free samples in the columns used previously in uranium leaching. The effects of increasing acid amounts and increasing leach liquor recycles on Th (and P/sub 2/O/sub 5/) leaching efficiency were studied.

  12. Cyclopentadienyl uranium, neptunium and plutonium chemistry

    International Nuclear Information System (INIS)

    Plews, M.J.

    1985-01-01

    The thesis presents the preparation and characterisation of a number of mono, bis and tris(cyclopentadienyl) complexes of uranium(IV), neptunium(IV) and plutonium(IV). The work of previous studies on mono(cyclopentadienyl) thorium and uranium complexes has been extended, and a range of isostructural neptunium species isolated. Their mode of formation and stability in tetrahydrofuran and acetonitrile solutions was investigated. (author)

  13. Determination of natural uranium in urine (233U)

    International Nuclear Information System (INIS)

    Jeanmaire, L.; Jammet, H.

    1959-01-01

    A procedure for the quantitative analysis of uranium in urine is described. The residue obtained by mineralization is dissolved in diluted hydrochloric acid. Uranium is separated by fixation on a permutit 50 column, elution with 0,2 M oxalic acid and electrodeposition on nickel. Uranium is then measured by α counting. It is thus possible to detect less than 1 pico-curie of uranium in the sample. (author) [fr

  14. Uranium concentrations in groundwater, northeastern Washington

    Science.gov (United States)

    Kahle, Sue C.; Welch, Wendy B.; Tecca, Alison E.; Eliason, Devin M.

    2018-04-18

    88,600 μg/L, and the median concentration of uranium in groundwater for all sites was 1.4 μg/L.New (2017) uranium in groundwater concentration data were obtained by sampling 13 private domestic wells for uranium in areas without recent (2000s) water-quality data. Uranium was detected in all 13 wells sampled for this study; concentrations ranged from 1.03 to 1,180 μg/L with a median of 22 μg/L. Uranium concentrations of groundwater samples from 6 of the 13 wells exceeded the MCL for uranium. Uranium concentrations in water samples from two wells were 1,130 and 1,180 μg/L, respectively; nearly 40 times the MCL.Additional data collection and analysis are needed in rural areas where self-supplied groundwater withdrawals are the primary source of water for human consumption. Of the roughly 43,000 existing water wells in the study area, only 1,755 wells, as summarized in this document, have available uranium concentration data, and some of those data are decades old. Furthermore, analysis of area groundwater quality would benefit from a more extensive chemical-analysis suite including general chemistry in order to better understand local geochemical conditions that largely govern the mobility of uranium. Although the focus of the present study is uranium, it also is important to recognize that there are other radionuclides of concern that may be present in area groundwater.

  15. A clean environment approach to uranium mining

    International Nuclear Information System (INIS)

    Grancea, Luminita

    2015-01-01

    A global and multi-faceted response to climate change is essential if meaningful and cost-effective progress is to be made in reducing the effects of climate change around the world. There is no doubt that the uranium mining sector has an important role to play in such a goal. Uranium is the raw material used to produce fuel for long-lived nuclear facilities, necessary for the generation of significant amounts of baseload low-carbon electricity for decades to come. Given expectations of growth in nuclear generating capacity and the associated uranium demand, enhancing awareness of leading practices in uranium mining is indispensable. Actors in the uranium mining sector operate in a complex world, throughout different geographies, and involving global supply chains. They manage climate-sensitive water, land and energy resources and balance the interests of various stakeholders. Managed well, uranium mining delivers sustainable value for economic growth, employment and infrastructure, with specific attention given to the preservation of the environment. In the early phases of the industry, however, downside risks existed, which created legacy environmental and health issues that still can be recalled today. This article addresses key aspects of modern uranium mining operations that have been introduced as regulations and practices have evolved in response to societal attitudes about health, safety and environmental protection. Such aspects of mine management were seldom, if ever, respected in the early stages of uranium mining. With the implementation of modern mine lifecycle parameters and regulatory requirements, uranium mining has become a leader in safety and environmental management. Today, uranium mining is conducted under significantly different circumstances and is now the most regulated and one of the safest forms of mining in the world. Experiences from modern uranium mines show that successful companies develop innovative strategies to manage all the

  16. Uranium-contaminated soil pilot treatment study

    International Nuclear Information System (INIS)

    Turney, W.R.J.R.; Mason, C.F.V.; Michelotti, R.A.

    1996-01-01

    A pilot treatment study is proving to be effective for the remediation of uranium-contaminated soil from a site at the Los Alamos National Laboratory by use of a two-step, zero-discharge, 100% recycle system. Candidate uranium-contaminated soils were characterized for uranium content, uranium speciation, organic content, size fractionization, and pH. Geochemical computer codes were used to forecast possible uranium leach scenarios. Uranium contamination was not homogenous throughout the soil. In the first step, following excavation, the soil was sorted by use of the ThemoNuclean Services segmented gate system. Following the sorting, uranium-contaminated soil was remediated in a containerized vat leach process by use of sodium-bicarbonate leach solution. Leach solution containing uranium-carbonate complexes is to be treated by use of ion-exchange media and then recycled. Following the treatment process the ion exchange media will be disposed of in an approved low-level radioactive landfill. It is anticipated that treated soils will meet Department of Energy site closure guidelines, and will be given open-quotes no further actionclose quotes status. Treated soils are to be returned to the excavation site. A volume reduction of contaminated soils will successfully be achieved by the treatment process. Cost of the treatment (per cubic meter) is comparable or less than other current popular methods of uranium-contamination remediation

  17. Removal of uranium from uranium plant wastewater using zero-valent iron in an ultrasonic field

    Energy Technology Data Exchange (ETDEWEB)

    Li, Jing; Zhang, Libo; Peng, Jinhui; Ma, Aiyuan; Xia, Hong Ying; Guo, Wen Qian; Yu, Xia [Yunnan Provincial Key Laboratory of Intensification Metallurgy, Kunming (China); Hu, Jinming; Yang, Lifeng [Nuclear Group Two Seven Two Uranium Industry Limited Liability Company, Hengyang (China)

    2016-06-15

    Uranium removal from uranium plant wastewater using zero-valent iron in an ultrasonic field was investigated. Batch experiments designed by the response surface methodology (RSM) were conducted to study the effects of pH, ultrasonic reaction time, and dosage of zero-valent iron on uranium removal efficiency. From the experimental data obtained in this work, it was found that the ultrasonic method employing zero-valent iron powder effectively removes uranium from uranium plant wastewater with a uranium concentration of 2,772.23 μg/L. The pH ranges widely from 3 to 7 in the ultrasonic field, and the prediction model obtained by the RSM has good agreement with the experimental results.

  18. Uranium price reporting systems

    International Nuclear Information System (INIS)

    1987-09-01

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

  19. Uranium Industry Annual, 1992

    International Nuclear Information System (INIS)

    1993-01-01

    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

  20. Uranium Industry Annual, 1992

    Energy Technology Data Exchange (ETDEWEB)

    1993-10-28

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