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Sample records for ten thorium uranium

  1. ELECTROLYSIS OF THORIUM AND URANIUM

    Science.gov (United States)

    Hansen, W.N.

    1960-09-01

    An electrolytic method is given for obtaining pure thorium, uranium, and thorium-uranium alloys. The electrolytic cell comprises a cathode composed of a metal selected from the class consisting of zinc, cadmium, tin, lead, antimony, and bismuth, an anode composed of at least one of the metals selected from the group consisting of thorium and uranium in an impure state, and an electrolyte composed of a fused salt containing at least one of the salts of the metals selected from the class consisting of thorium, uranium. zinc, cadmium, tin, lead, antimony, and bismuth. Electrolysis of the fused salt while the cathode is maintained in the molten condition deposits thorium, uranium, or thorium-uranium alloys in pure form in the molten cathode which thereafter may be separated from the molten cathode product by distillation.

  2. Rays Emitted by Compounds of Uranium and of Thorium

    Indian Academy of Sciences (India)

    27 from 2 to 14. 20. 11 from 3 to 7 very active. All the uranium compounds studied are active, and are, in general, more active to the extent that they contain more uranium. The compounds of thorium are very active. Thorium oxide surpasses even metallic uranium in activity. It is remarkable that the two most active elements, ...

  3. Evolution of uranium and thorium minerals

    Science.gov (United States)

    Hazen, R. M.; Ewing, R. C.; Sverjensky, D. A.

    2009-12-01

    The origins and near-surface distributions of the approximately 250 known uranium and/or thorium minerals elucidate principles of mineral evolution. This history can be divided into four phases. The first, from ~4.5 to 3.5 Ga, involved successive concentrations of uranium and thorium from their initial uniform trace distribution into magmatic-related fluids from which the first U4+ and Th4+ minerals, uraninite (UO2), thorianite (ThO2) and coffinite (USiO4), precipitated in the crust. The second period, from ~3.5 to 2.2 Ga, saw the formation of large low-grade concentrations of detrital uraninite (containing several weight percent Th) in the Witwatersrand-type quartz-pebble conglomerates deposited in a highly anoxic fluvial environment. Abiotic alteration of uraninite and coffinite, including radiolysis and auto-oxidation caused by radioactive decay and the formation of helium from alpha particles, may have resulted in the formation of a limited suite of uranyl oxide-hydroxides. Earth’s third phase of uranium mineral evolution, during which most known U minerals first precipitated from reactions of soluble uranyl (U6+O2)2+ complexes, followed the Great Oxidation Event (GOE) at ~2.2 Ga and thus was mediated indirectly by biologic activity. Most uraninite deposited during this phase was low in Th and precipitated from saline and oxidizing hydrothermal solutions (100 to 300°C) transporting (UO2)2+-chloride complexes. Examples include the unconformity- and vein-type U deposits (Australia and Canada) and the unique Oklo natural nuclear reactors in Gabon. The onset of hydrothermal transport of (UO2)2+ complexes in the upper crust may reflect the availability of CaSO4-bearing evaporites after the GOE. During this phase, most uranyl minerals would have been able to form in the O2-bearing near-surface environment for the first time through weathering processes. The fourth phase of uranium mineralization began approximately 400 million years ago, as the rise of land plants

  4. Bioaccumulation of uranium and thorium from the solution containing both elements using various microorganisms

    Energy Technology Data Exchange (ETDEWEB)

    Tsuruta, T. [Department of Applied Chemistry, Tohwa University, 1-1-1 Chikushigaoka, Fukuoka 815-8510 (Japan)]. E-mail: ttsuruta@tohwa-u.ac.jp

    2006-02-09

    The effects of proton, thorium and uranium on the bioaccumulation of thorium and uranium from the solution (pH 3.5) containing uranium and thorium using Streptomyces levoris cells were examined. The amount of thorium accumulated using the cells decreased by the pre-contact between the cells and the solution (pH 3.5) containing no metals, whereas that of uranium was almost unaffected by the treatment. The amount of thorium was almost unaffected by the existence of uranium. On the other hand, the amount of uranium accumulated was strongly affected by the thorium, especially thorium addition after uranium accumulation. The decrease of uranium accumulated by the addition of thorium after the accumulation of uranium was higher than that from the solution containing both elements. Therefore, the contribution of uranium-thorium exchange reaction was higher than that of competition reaction. Accordingly, proton-uranium-thorium exchange reaction was occurred in the accumulation of thorium from the solution containing thorium and uranium. The gram-positive bacteria, such as Micrococcus luteus, Arthrobacter nicotianae, Bacillus subtilis and B. megaterium, has a much higher separation factor as thorium/uranium than that of actinomycetes. These gram-positive bacterial strains can be used for the accumulation of thorium from the solution containing uranium and thorium.

  5. 49 CFR 173.434 - Activity-mass relationships for uranium and natural thorium.

    Science.gov (United States)

    2010-10-01

    ....434 Activity-mass relationships for uranium and natural thorium. The table of activity-mass relationships for uranium and natural thorium are as follows: Thorium and uranium enrichment 1(Wt% 235 U present... 49 Transportation 2 2010-10-01 2010-10-01 false Activity-mass relationships for uranium and...

  6. Uranium and thorium recovery in thorianite ore-preliminary results

    Energy Technology Data Exchange (ETDEWEB)

    Gaiotte, Joao V.M. [Universidade Federal de Alfenas, Pocos de Caldas, MG (Brazil); Villegas, Raul A.S.; Fukuma, Henrique T., E-mail: rvillegas@cnen.gov.br, E-mail: htfukuma@cnen.gov.br [Comissao Nacional de Energia Nuclear (CNEN), Pocos de Caldas, MG (Brazil). Lab. de Pocos de Caldas

    2011-07-01

    This work presents the preliminary results of the studies aiming to develop a hydrometallurgical process to produce uranium and thorium concentrates from thorianite ore from Amapa State, Brazil. This process comprises two major parts: acid leaching and Th/U recovery using solvent extraction strategies. Thorianite ore has a typical composition of 60 - 70% of thorium, 8 - 10% lead and 7 - 10% uranium. Sulfuric acid leaching operational conditions were defined as follows: acid/ore ratio 7.5 t/t, ore size below 65 mesh (Tyler), 2 hours leaching time and temperature of 100 deg C. Leaching tests results showed that uranium and thorium recovery exceeded 95%, whereas 97% of lead ore content remained in the solid form. Uranium and thorium simultaneous solvent extraction is necessary due to high sulfate concentration in the liquor obtained from leaching, so the Primene JM-T primary anime was used for this extraction step. Aqueous raffinate from extraction containing sulfuric acid was recycled to the leaching step, reducing acid uptake around 60%, to achieve a net sulfuric acid consumption of 3 t/t of ore. Uranium and thorium simultaneous stripping was performed using sodium carbonate solution. In the aqueous stripped it was added sulfuric acid at pH 1.5, followed by a second solvent extraction step using the tertiary amine Alamine 336. The following stripping step was done with a solution of sodium chloride, resulting in a final solution of 23 g L-1 uranium. (author)

  7. Distribution of uranium, thorium, and isotopic composition of uranium in soil samples of south Serbia: Evidence of depleted uranium

    OpenAIRE

    Sahoo Sarata Kumar; Fujimoto Kenzo; Čeliković Igor; Ujić Predrag; Žunić Zora S.

    2004-01-01

    Inductively coupled plasma mass spectrometry and thermal ionization mass spectrom - etry were used to measure concentration of uranium and thorium as well as isotopic composition of uranium respectively in soil samples collected around south Serbia. An analytical method was established for a routine sample preparation procedure for uranium and thorium. Uranium was chemically separated and purified from soil samples by anion exchange resin and UTEVA extraction chromatography and its isotopic c...

  8. Landscape control of uranium and thorium in boreal streams – spatiotemporal variability and the role of wetlands

    Directory of Open Access Journals (Sweden)

    F. Lidman

    2012-11-01

    Full Text Available The concentrations of uranium and thorium in ten partly nested streams in the boreal forest region were monitored over a two-year period. The investigated catchments ranged from small headwaters (0.1 km2 up to a fourth-order stream (67 km2. Considerable spatiotemporal variations were observed, with little or no correlation between streams. The fluxes of both uranium and thorium varied substantially between the subcatchments, ranging from 1.7 to 30 g km−2 a−1 for uranium and from 3.2 to 24 g km−2 a−1 for thorium. Airborne gamma spectrometry was used to measure the concentrations of uranium and thorium in surface soils throughout the catchment, suggesting that the concentrations of uranium and thorium in mineral soils are similar throughout the catchment. The fluxes of uranium and thorium were compared to a wide range of parameters characterising the investigated catchments and the chemistry of the stream water, e.g. soil concentrations of these elements, pH, TOC (total organic carbon, Al, Si and hydrogen carbonate, but it was concluded that the spatial variabilities in the fluxes of both uranium and thorium mainly were controlled by wetlands. The results indicate that there is a predictable and systematic accumulation of both uranium and thorium in boreal wetlands that is large enough to control the transport of these elements. On the landscape scale approximately 65–80% of uranium and 55–65% of thorium entering a wetland were estimated to be retained in the peat. Overall, accumulation in mires and other types of wetlands was estimated to decrease the fluxes of uranium and thorium from the boreal forest landscape by 30–40%, indicating that wetlands play an important role for the biogeochemical cycling of uranium and thorium in the boreal forest landscape. The atmospheric deposition of uranium and thorium was also quantified, and its contribution to boreal streams was

  9. Thorium and Uranium in the Rock Raw Materials Used For the Production of Building Materials

    Science.gov (United States)

    Pękala, Agnieszka

    2017-10-01

    Thorium and uranium are constant components of all soils and most minerals thereby rock raw materials. They belong to the particularly dangerous elements because of their natural radioactivity. Evaluation of the content of the radioactive elements in the rock raw materials seems to be necessary in the early stage of the raw material evaluation. The rock formations operated from deposits often are accumulated in landfills and slag heaps where the concentration of the radioactive elements can be many times higher than under natural conditions. In addition, this phenomenon may refer to buildings where rock raw materials are often the main components of the construction materials. The global control system of construction products draws particular attention to the elimination of used construction products containing excessive quantities of the natural radioactive elements. In the presented study were determined the content of thorium and uranium in rock raw materials coming from the Bełachatów lignite deposit. The Bełchatów lignite deposit extracts mainly lignite and secondary numerous accompanying minerals with the raw material importance. In the course of the field works within the framework of the carried out work has been tested 92 samples of rocks of varied petrographic composition. There were carried out analyses of the content of the radioactive elements for 50 samples of limestone of the Jurassic age, 18 samples of kaolinite clays, and 24 samples of siliceous raw materials, represented by opoka-rocks, diatomites, gaizes and clastic rocks. The measurement of content of the natural radioactive elements thorium and uranium based on measuring the frequency counts of gamma quantum, recorded separately in measuring channels. At the same time performed measurements on volume patterns radioactive: thorium and uranium. The studies were carried out in Mazar spectrometer on the powdered material. Standardly performed ten measuring cycles, after which were calculated

  10. Experimental determination of uranium and thorium in Allchar ore

    Science.gov (United States)

    Ljubičić, A.; Krčmar, M.; Kaučić, S.; Logan, B. A.

    1988-08-01

    In addition to its production in the 205Tl(ν, e -) 205Pb reaction 205Pb can be produced in the Allchar mine by other reaction chains which are initiated by cosmic rays, and by alpha particles from the decay chains of uranium and thorium present in the lorandite and other ores found in the mine. We have measured the uranium and thorium concentrations in lorandite, realgar and marcasite samples from the mine by observing fission fragments produced in neutron induced fission. The fragments were recorded in Makrofol KG film and the measurement technique has a good level of sensitivity. Excellent discrimination against other radiations is obtained.

  11. Uranium- and thorium-bearing pegmatites of the United States

    Energy Technology Data Exchange (ETDEWEB)

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

    1980-04-01

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

  12. Uranium, thorium and potassium in Indian rocks and ores

    Indian Academy of Sciences (India)

    Abstract. Usinglsodiurn iodide gamma-ray spectrometer, the radioactivity content of the crustal material from various places in India has been estimated. “Sedi- mentary and metamorphic rocks contain more uranium and. thorium than igneous rocks. PhoSphate rocks and ores from Kerala region contain higher nranir m and.

  13. Concentrations of Uranium,Thorium and Potassium in Sweden

    Energy Technology Data Exchange (ETDEWEB)

    Thunholm, Bo; Linden, Anders H.; Gustafsson, Bosse [Geological Survey of Sweden, Uppsala (Sweden)

    2005-04-01

    This report is largely a result of the Swedish contribution to an IAEA co-ordinated research programme (CRP) on the use of selected safety indicators in the assessment of radioactive waste disposal. The CRP was focusing on the assessment of the longterm safety of radioactive waste disposal by means of additional safety indicators based on data from natural systems with emphasis on description of existing data on radioactive elements and radionuclides. A major part of the work was focused on collecting data on geophysics as well as geochemistry and groundwater chemistry; mainly uranium (U), thorium (Th) and potassium (K). Data were interpreted resulting in maps and statistical description.

  14. Photon attenuation properties of some thorium, uranium and plutonium compounds

    Energy Technology Data Exchange (ETDEWEB)

    Singh, V. P.; Badiger, N. M. [Karnatak University, Department of Physics, Dharwad-580003, Karnataka (India); Vega C, H. R., E-mail: kudphyvps@rediffmail.com [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Cipres No. 10, Fracc. La Penuela, 98068 Zacatecas, Zac. (Mexico)

    2015-10-15

    Mass attenuation coefficients, effective atomic numbers, effective electron densities for nuclear materials; thorium, uranium and plutonium compounds have been studied. The photon attenuation properties for the compounds have been investigated for partial photon interaction processes by photoelectric effect, Compton scattering and pair production. The values of these parameters have been found to change with photon energy and interaction process. The variations of mass attenuation coefficients, effective atomic number and electron density with energy are shown graphically. Moreover, results have shown that these compounds are better shielding and suggesting smaller dimensions. The study would be useful for applications of these materials for gamma ray shielding requirement. (Author)

  15. Laser-induced breakdown spectroscopy measurements of uranium and thorium powders and uranium ore

    Energy Technology Data Exchange (ETDEWEB)

    Judge, Elizabeth J. [Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Barefield, James E., E-mail: jbarefield@lanl.gov [Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Berg, John M. [Manufacturing Engineering and Technology Division, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Clegg, Samuel M.; Havrilla, George J.; Montoya, Velma M.; Le, Loan A.; Lopez, Leon N. [Chemistry Division, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States)

    2013-05-01

    Laser-induced breakdown spectroscopy (LIBS) was used to analyze depleted uranium and thorium oxide powders and uranium ore as a potential rapid in situ analysis technique in nuclear production facilities, environmental sampling, and in-field forensic applications. Material such as pressed pellets and metals, has been extensively studied using LIBS due to the high density of the material and more stable laser-induced plasma formation. Powders, on the other hand, are difficult to analyze using LIBS since ejection and removal of the powder occur in the laser interaction region. The capability of analyzing powders is important in allowing for rapid analysis of suspicious materials, environmental samples, or trace contamination on surfaces since it most closely represents field samples (soil, small particles, debris etc.). The rapid, in situ analysis of samples, including nuclear materials, also reduces costs in sample collection, transportation, sample preparation, and analysis time. Here we demonstrate the detection of actinides in oxide powders and within a uranium ore sample as both pressed pellets and powders on carbon adhesive discs for spectral comparison. The acquired LIBS spectra for both forms of the samples differ in overall intensity but yield a similar distribution of atomic emission spectral lines. - Highlights: • LIBS analysis of mixed actinide samples: depleted uranium oxide and thorium oxide • LIBS analysis of actinide samples in powder form on carbon adhesive discs • Detection of uranium in a complex matrix (uranium ore) as a precursor to analyzing uranium in environmental samples.

  16. Biomonitoring of environmental pollution by thorium and uranium in selected regions of the Republic of Kazakhstan.

    Science.gov (United States)

    Zoriy, P; Ostapczuk, P; Dederichs, H; Höbig, J; Lennartz, R; Zoriy, M

    2010-05-01

    Two former uranium mines and a uranium reprocessing factory in the city of Aktau, Kazakhstan, may represent a risk of contaminating the surrounding areas by uranium and its daughter elements. One of the possible fingerprinting tools for studying the environmental contamination is using plant samples, collected in the surroundings of this city in 2007 and 2008. The distribution pattern of environmental pollution by uranium and thorium was evaluated by determining the thorium and uranium concentrations in plant samples (Artemisia austriaca) from the city of Aktau and comparing these results with those obtained for the same species of plants from an unpolluted area (town of Kurchatov). The determination of the uranium and thorium concentrations in different parts of A. austriaca plants collected from the analyzed areas demonstrated that the main contamination of the flora in areas surrounding the city of Aktau was due to dust transported by the wind from the uranium mines. The results obtained demonstrate that all the areas surrounding Aktau have a higher pollution level due to thorium and uranium than the control area (Kurchatov). A few "hot points" with high concentrations of uranium and thorium were found near the uranium reprocessing factory and the uranium mines. Copyright (c) 2010 Elsevier Ltd. All rights reserved.

  17. Critical review of analytical techniques for safeguarding the thorium-uranium fuel cycle

    Energy Technology Data Exchange (ETDEWEB)

    Hakkila, E.A.

    1978-10-01

    Conventional analytical methods applicable to the determination of thorium, uranium, and plutonium in feed, product, and waste streams from reprocessing thorium-based nuclear reactor fuels are reviewed. Separations methods of interest for these analyses are discussed. Recommendations concerning the applicability of various techniques to reprocessing samples are included. 15 tables, 218 references.

  18. The contents of uranium and thorium in the dominating kinds of plants of the Central Caucasus

    Directory of Open Access Journals (Sweden)

    T. A. Asvarova

    2008-01-01

    Full Text Available The result of this work have shown that the difference of contents uranium and thorium of various plants of Great Caucasus dependents views plants, on various types rock, type of soils and physicalchemicalproperties of soil. The maximum concentration of uranium and thorium are registered in Saxifraga mochata, S. Dinikii, S. exarata, S. carinata, and the minimum concentration is in Veratrum Lobelianum.

  19. The structural and genetic position uranium-thorium mineralization of Azov megablock

    Directory of Open Access Journals (Sweden)

    Katalenets A.I.

    2014-12-01

    Full Text Available The genetic characteristics of development and placement uranium-thorium mineralization and distribution of their concentrations in Azov megablock areas are examined. The main structures of Azov megablock areas controlling of distribution of metasomatic types and ore occurrence related with them are set. Preliminary basis for the allocation of boundaries and areas of ore districts is created. Considered theoretical and practical problem associated with the establishment of regional characteristics, genetic types of mineralization, its structural and temporary accommodation, the development of search criteria and characteristics of mineralization, the release of potentially mineralized areas and study areas of prospecting for Azov megablock of Ukrainian shield. The research is based on data on the geological structure of the PM, and the structural control of the placement lithochemical uranium and thorium anomalies occurrences and deposits, typomorphic properties of minerals, the phase distribution of uranium, thorium. Distribution of uranium and thorium mineralization in areas considered structure is: own minerals, isomorphic impurity in minerals associated with them, or turn on the first to the last. Uranium and thorium PM mineralization is characterized by a genetic (paragenetic involving mineral associations exogenous and metasomatic rocks.

  20. Alpha-spectrometric analysis of uranium and thorium using solid-phase extraction for sample preparation

    Energy Technology Data Exchange (ETDEWEB)

    Weber, R.; Esterlund, R.A.; Patzelt, P

    1999-05-01

    A method is presented here for the preparation of thin uniform samples of naturally occurring uranium and thorium which are highly suitable for {alpha}-spectrometric analysis. The solid-phase extraction procedure simultaneously achieves a complete separation of the analytes from the sample matrix and a high enrichment factor for uranium and thorium, so that the ensuing eluate is ideally suited for either electrodeposition or ICP-MS, without the need for complicated and painstaking sample preparation. In contrast to conventional liquid-liquid phase-extraction methods, no organic waste solutions are produced, and the process can be easily automated.

  1. Smart thorium and uranium determination exploiting renewable solid-phase extraction applied to environmental samples in a wide concentration range

    Energy Technology Data Exchange (ETDEWEB)

    Avivar, Jessica; Ferrer, Laura; Cerda, Victor [University of the Balearic Islands, Chemistry Department, Palma (Spain); Casas, Montserrat [University of the Balearic Islands, Physic Department, IFISC-CSIC, Palma (Spain)

    2011-07-15

    A smart fully automated system is proposed for determination of thorium and uranium in a wide concentration range, reaching environmental levels. The hyphenation of lab-on-valve (LOV) and multisyringe flow injection analysis (MSFIA), coupled to a long path length liquid waveguide capillary cell, allows the spectrophotometric determination of thorium and uranium in different types of environmental sample matrices achieving high selectivity and sensitivity levels. Online separation and preconcentration of thorium and uranium is carried out by means of Uranium and TEtraValents Actinides resin. The potential of the LOV-MSFIA makes possible the full automation of the system by the in-line regeneration of the column and its combination with a smart methodology is a step forward in automation. After elution, thorium(IV) and uranium(VI) are spectrophotometrically detected after reaction with arsenazo-III. We propose a rapid, inexpensive, and fully automated method to determine thorium(IV) and uranium(VI) in a wide concentration range (0-1,200 and 0-2,000 {mu}g L{sup -1} Th and U, respectively). Limits of detection reached are 5.9 {eta}g L{sup -1} of uranium and 60 {eta}g L{sup -1} of thorium. Different water sample matrices (seawater, well water, freshwater, tap water, and mineral water), and a channel sediment reference material which contained thorium and uranium were satisfactorily analyzed with the proposed method. (orig.)

  2. Determination of isotopes of uranium and thorium in low-level environmental samples

    Energy Technology Data Exchange (ETDEWEB)

    Acena, M.L. (CIEMAT, Inst. de Investigacion Basica, Metrologia. Ed. 3, Madrid (Spain)); Crespo, M.T. (CIEMAT, Inst. de Investigacion Basica, Metrologia. Ed. 3, Madrid (Spain)); Galan, M.P. (CIEMAT, Inst. de Investigacion Basica, Metrologia. Ed. 3, Madrid (Spain)); Gascon, J.L. (CIEMAT, Inst. de Investigacion Basica, Metrologia. Ed. 3, Madrid (Spain))

    1994-01-22

    Different sample treatments and separation procedures are set up and compared for the analysis of uranium and thorium in coal, sediments, water and plant samples. Some considerations about the alpha-spectrometric measurements and the radioactive tracers used as yield determinants of the chemical process are presented. (orig.)

  3. 77 FR 3460 - Reimbursement for Costs of Remedial Action at Active Uranium and Thorium Processing Sites

    Science.gov (United States)

    2012-01-24

    ...] [FR Doc No: 2012-1352] DEPARTMENT OF ENERGY Reimbursement for Costs of Remedial Action at Active... (DOE) acceptance of claims in FY 2012 from eligible active uranium and thorium processing site.... 112-10); and the remaining $100,000 had been obligated for Title X audit support. No funds were...

  4. Biogeochemical investigation in south eastern Andhra Pradesh: the distribution of rare earths, thorium and uranium in plants and soils

    Energy Technology Data Exchange (ETDEWEB)

    Raju, K.K.; Raju, A.N. [Sri Venkateswara Univ., Tirupati (India). Dept. of Geology

    2000-09-01

    The concentration of rare earth elements (REE), thorium and uranium were determined by inductively coupled plasma mass spectrometry (ICP-MS) in the plant species, Pterocarpus santalinus, P. marsupium and P. dalbergioides, and the soils on which they were growing. Higher concentrations of lanthanum (La), cerium (Ce) were observed in both plants and soils. Large amounts of thorium and uranium were found in the soil. In all tree species, the concentration of REEs were higher in the heartwood than the leaves. The heartwood of P. santalinus accumulated larger quantities of uranium (average concentration of 1.22 ppm) and thorium (mean value of 2.57 ppm) than the other two species. (orig.)

  5. Arbuscular mycorrhiza reduces phytoextraction of uranium, thorium and other elements from phosphate rock

    DEFF Research Database (Denmark)

    Roos, Per; Jakobsen, Iver

    2008-01-01

    Uptake of metals from uranium-rich phosphate rock was studied in Medicago truncatula plants grown in symbiosis with the arbuscular mycorrhizal fungus Glomus intraradices or in the absence of mycorrhizas. Shoot concentrations of uranium and thorium were lower in mycorrhizal than in non-mycorrhizal......Uptake of metals from uranium-rich phosphate rock was studied in Medicago truncatula plants grown in symbiosis with the arbuscular mycorrhizal fungus Glomus intraradices or in the absence of mycorrhizas. Shoot concentrations of uranium and thorium were lower in mycorrhizal than in non......-mycorrhizal plants and root-to-shoot ratio of most metals was increased by mycorrhizas. This protective role of mycorrhizas was observed even at very high supplies of phosphate rock. In contrast, phosphorus uptake was similar at all levels of phosphate rock, suggesting that the P was unavailable to the plant......-fungus uptake systems. The results support the role of arbuscular mycorrhiza as being an important component in phytostabilization of uranium. This is the first study to report on mycorrhizal effect and the uptake and root-to-shoot transfer of thorium from phosphate rock. (c) 2007 Elsevier Ltd. All rights...

  6. Arbuscular mycorrhiza reduces phytoextraction of uranium, thorium and other elements from phosphate rock

    Energy Technology Data Exchange (ETDEWEB)

    Roos, Per [Radiation Research Department, Riso National Laboratory, Technical University of Denmark, DK-4000 Roskilde (Denmark); Jakobsen, Iver [Biosystems Department, Riso National Laboratory, Technical University of Denmark, DK-4000 Roskilde (Denmark)], E-mail: iver.jakobsen@risoe.dk

    2008-05-15

    Uptake of metals from uranium-rich phosphate rock was studied in Medicago truncatula plants grown in symbiosis with the arbuscular mycorrhizal fungus Glomus intraradices or in the absence of mycorrhizas. Shoot concentrations of uranium and thorium were lower in mycorrhizal than in non-mycorrhizal plants and root-to-shoot ratio of most metals was increased by mycorrhizas. This protective role of mycorrhizas was observed even at very high supplies of phosphate rock. In contrast, phosphorus uptake was similar at all levels of phosphate rock, suggesting that the P was unavailable to the plant-fungus uptake systems. The results support the role of arbuscular mycorrhiza as being an important component in phytostabilization of uranium. This is the first study to report on mycorrhizal effect and the uptake and root-to-shoot transfer of thorium from phosphate rock.

  7. Thorium

    Science.gov (United States)

    Wickleder, Mathias S.; Fourest, Blandine; Dorhout, Peter K.

    In 1815 Berzelius analyzed a rare mineral from the Falun district. He assumed that the mineral contained a new element, which he named thorium after the ancient Scandinavian god of thunder and weather, Thor (Weeks and Leicester, 1968).

  8. Determination of uranium and thorium contents inside different materials using track detectors and mean critical angles

    CERN Document Server

    Misdaq, M A; Ktata, A; Merzouki, A; Youbi, N

    1999-01-01

    The critical angles of the CR-39 (theta sub c) and LR-115 type II (theta sub c ') solid state nuclear track detectors (SSNTD) for detecting alpha-particles emitted by the uranium and thorium series have been evaluated by calculating the corresponding ranges of the emitted alpha-particles in different material samples and in the SSNTD studied. The influence of the emitted alpha-particles initial and residual energies on the critical angles of the SSNTD studied has been investigated. The uranium and thorium contents of different geological samples have been evaluated by exploiting data obtained for the critical angles of the CR-39 and LR-115 type II solid state nuclear track detectors and measuring the corresponding densities of tracks.

  9. Autoradiography of geological fluorite samples for determination of uranium and thorium distribution using nuclear track methodology

    Energy Technology Data Exchange (ETDEWEB)

    Pi, T.; Sole, J. [Instituto de Geologia, UNAM, Cd. Universitaria, Coyoacan, 04510 Mexico DF (Mexico); Golzarri, J.I; Rickards, J.; Espinosa, G. [IFUNAM, AP 20-364, 01000 Mexico DF (Mexico)]. e-mail: espinosa@fisica.unam.mx

    2007-07-01

    In this paper we present the uranium and thorium distribution analysis of several samples of the 'La Azul' an epithermal fluorspar deposit in southern Mexico, using nuclear track methodology (NTM), in the alpha-autoradiography mode, by placing the mineral sample in contact with a polycarbonate detector. This constitutes a non-destructive analysis, with sufficient sensitivity to provide valuable information about textural and para genetic characteristics of the geological samples. The selected nuclear track detector was CR-39 (Landauer). The region of interest of the geological samples was polished and put in contact with the detector material surface for 45 days in a vacuum chamber (10-3 torr). After this period of time, the detectors were chemically etched, revealing the auto radiograph of the radioactive material. The results show a clear distribution of bands of uranium and thorium in the fluorite samples. This is valuable information for the genetic or geochronological studies of the ore deposits. (Author)

  10. Sorption of Uranium(VI and Thorium(IV by Jordanian Bentonite

    Directory of Open Access Journals (Sweden)

    Fawwaz I. Khalili

    2013-01-01

    Full Text Available Purification of raw bentonite was done to remove quartz. This includes mixing the raw bentonite with water and then centrifuge it at 750 rpm; this process is repeated until white purified bentonite is obtained. XRD, XRF, FTIR, and SEM techniques will be used for the characterization of purified bentonite. The sorption behavior of purified Jordanian bentonite towards and Th4+ metal ions in aqueous solutions was studied by batch experiment as a function of pH, contact time, temperature, and column techniques at 25.0∘C and . The highest rate of metal ions uptake was observed after 18 h of shaking, and the uptake has increased with increasing pH and reached a maximum at . Bentonite has shown high metal ion uptake capacity toward uranium(VI than thorium(IV. Sorption data were evaluated according to the pseudo- second-order reaction kinetic. Sorption isotherms were studied at temperatures 25.0∘C, 35.0∘C, and 45.0∘C. The Langmuir, Freundlich, and Dubinin-Radushkevich (D-R sorption models equations were applied and the proper constants were derived. It was found that the sorption process is enthalpy driven for uranium(VI and thorium(IV. Recovery of uranium(VI and thorium(IV ions after sorption was carried out by treatment of the loaded bentonite with different concentrations of HNO3 1.0 M, 0.5 M, 0.1 M, and 0.01 M. The best percent recovery for uranium(VI and thorium(IV was obtained when 1.0 M HNO3 was used.

  11. Feasibility study of boiling water reactor core based on thorium-uranium fuel concept

    Energy Technology Data Exchange (ETDEWEB)

    Nunez-Carrera, Alejandro [Comision Nacional de Seguridad Nuclear y Salvaguardias, Dr. Barragan 779, Col Narvarte, 03020 Mexico D.F. (Mexico); Francois Lacouture, Juan Luis; Martin del Campo, Cecilia [Universidad Nacional Autonoma de Mexico, Facultad de Ingenieria, Paseo Cuauhnahuac 8532, Jiutepec, Mor. (Mexico); Espinosa-Paredes, Gilberto [Area de Ingenieria en Recursos Energeticos, Universidad Autonoma Metropolitana Iztapalapa, Apartado Postal 55-534, Mexico D.F. 09340 (Mexico)], E-mail: gepe@xanum.uam.mx

    2008-01-15

    The design of a boiling water reactor (BWR) equilibrium core using the thorium-uranium (blanket-seed) concept in the same integrated fuel assembly is presented in this paper. The lattice design uses the thorium conversion capability to {sup 233}U in a BWR spectrum. A core design was developed to achieve an equilibrium cycle of one effective full power year in a standard BWR with a reload of 104 fuel assemblies designed with an average {sup 235}U enrichment of 7.5 w/o in the seed sub-lattice. The main core operating parameters were obtained. It was observed that the analyzed parameters behave like those obtained in a standard BWR. The economic analysis shows that the fuel cycle cost of the proposed core design can be competitive with a standard uranium core design. Finally, a comparison of the toxicity of the spent fuel showed that the toxicity is lower in the thorium cycle than in other fuel cycles (UO{sub 2} and MOX uranium and plutonium) in the case of the once through cycle for light water reactors (LWR)

  12. Electrodeposition of uranium and thorium onto small platinum electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Reichenberger, Michael A., E-mail: mar89@ksu.edu [S.M.A.R.T. Laboratory, Mechanical and Nuclear Engineering Dept., Kansas State University, Manhattan, KS 66506 (United States); Ito, Takashi [Department of Chemistry, Kansas State University, 213 CBC Building, Manhattan, KS 66506-0401 (United States); Ugorowski, Philip B.; Montag, Benjamin W.; Stevenson, Sarah R.; Nichols, Daniel M.; McGregor, Douglas S. [S.M.A.R.T. Laboratory, Mechanical and Nuclear Engineering Dept., Kansas State University, Manhattan, KS 66506 (United States)

    2016-03-11

    Preparation of thin U- and Th-coated 0.3 mm diameter Pt working electrodes by the cyclic potential sweep method is described. Uranyl- and thorium hydroxide layers were electrodeposited from ethanol solutions containing 0.02 M natural uranyl and 0.02 M natural thorium nitrate, each with 3.6 M ammonium nitrate. The cell for electrodeposition was specially developed in order to accommodate the small working electrodes for this research by including a working electrode probe, 3-D translation stage, and microscope. The source material deposition was analyzed using digital microscopy and scanning electron microscopy, and confirmed using x-ray fluorescence measurements. The appropriate potential range for electrodeposition was determined to be −0.62 V to −0.64 V for a 0.3 mm diameter Pt working electrode placed 1 cm from the counter electrode. Smooth, uniform deposition was observed near the central region of the working electrode, while surface cracking and crystalline formations were found near the edge of the working electrode. The final procedure for sample substrate preparation, electrolytic solution preparation and electrodeposition are described.

  13. Electrodeposition of uranium and thorium onto small platinum electrodes

    Science.gov (United States)

    Reichenberger, Michael A.; Ito, Takashi; Ugorowski, Philip B.; Montag, Benjamin W.; Stevenson, Sarah R.; Nichols, Daniel M.; McGregor, Douglas S.

    2016-03-01

    Preparation of thin U- and Th-coated 0.3 mm diameter Pt working electrodes by the cyclic potential sweep method is described. Uranyl- and thorium hydroxide layers were electrodeposited from ethanol solutions containing 0.02 M natural uranyl and 0.02 M natural thorium nitrate, each with 3.6 M ammonium nitrate. The cell for electrodeposition was specially developed in order to accommodate the small working electrodes for this research by including a working electrode probe, 3-D translation stage, and microscope. The source material deposition was analyzed using digital microscopy and scanning electron microscopy, and confirmed using x-ray fluorescence measurements. The appropriate potential range for electrodeposition was determined to be -0.62 V to -0.64 V for a 0.3 mm diameter Pt working electrode placed 1 cm from the counter electrode. Smooth, uniform deposition was observed near the central region of the working electrode, while surface cracking and crystalline formations were found near the edge of the working electrode. The final procedure for sample substrate preparation, electrolytic solution preparation and electrodeposition are described.

  14. Transient and stability analysis of a BWR core with thorium-uranium fuel

    Energy Technology Data Exchange (ETDEWEB)

    Nunez-Carrera, Alejandro [Comision Nacional de Seguridad Nuclear y Salvaguardias, Dr. Barragan 779 Col. Narvarte, 03020 Mexico, DF (Mexico); Espinosa-Paredes, Gilberto [Division de Ciencias Basicas e Ingenieria, Universidad Autonoma Metropolitana, Av. San Rafael Atlixco 186, Col. Vicentina, 09340 Mexico, DF (Mexico)], E-mail: gepe@xanum.uam.mx; Francois, Juan-Luis [Departamento de Sistemas Energeticos, Facultad de Ingenieria, Universidad Nacional Autonoma de Mexico, Paseo Cuauhnahuac 8532, 62550 Jiutepec Mor. (Mexico)

    2008-08-15

    The kinetic response of a boiling water reactor (BWR) equilibrium core using thorium as a nuclear material, in an integrated blanket-seed assembly, is presented in this work. Additionally an in-house code was developed to evaluate this core under steady state and transient conditions including a stability analysis. The code has two modules: (a) the time domain module for transient analysis and (b) the frequency domain module for stability analysis. The thermal-hydraulic process is modeled by a set of five equations, considering no homogeneous flow with drift-flux approximation and non-equilibrium thermodynamic. The neutronic process is calculated with a point kinetics model. Typical BWR reactivity effects are considered: void fraction, fuel temperature, moderator temperature and control rod density. Collapsed parameters were included in the code to represent the core using an average fuel channel. For the stability analysis, in the frequency domain, the transfer function is determined by applying Laplace-transforming to the calculated pressure drop perturbations in each of the considered regions where a constant total pressure drop was considered. The transfer function was used to study the system response in the frequency domain when an inlet flow perturbation is applied. The results show that the neutronic behavior of the core with thorium uranium fuel is similar to a UO{sub 2} core, even during transient conditions. The stability and transient analysis show that the thorium-uranium fuel can be operated safely in current BWRs.

  15. Minimization of the fission product waste by using thorium based fuel instead of uranium dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Galahom, A. Abdelghafar, E-mail: Agalahom@yahoo.com

    2017-04-01

    This research discusses the neutronic characteristics of VVER-1200 assembly fueled with five different fuel types based on thorium. These types of fuel based on mixing thorium as a fertile material with different fissile materials. The neutronic characteristics of these fuels are investigated by comparing their neutronic characteristics with the conventional uranium dioxide fuel using the MCNPX code. The objective of this study is to reduce the production of long-lived actinides, get rid of plutonium component and to improve the fuel cycle economy while maintaining acceptable values of the neutronic safety parameters such as moderator temperature coefficient, Doppler coefficient and effective delayed neutrons (β). The thorium based fuel has a more negative Doppler coefficient than uranium dioxide fuel. The moderator temperature coefficient (MTC) has been calculated for the different proposed fuels. Also, the fissile inventory ratio has been calculated at different burnup step. The use of Th-232 as a fertile material instead of U-238 in a nuclear fuel is the most promising fuel in VVER-1200 as it is the ideal solution to avoid the production of more plutonium components and long-lived minor actinides. The reactor grade plutonium accumulated in light water reactor with burnup can be recycled by mixing it with Th-232 to fuel the VVER-1200 assembly. The concentrations of Xe-135 and Sm-151 have been investigated, due to their high thermal neutron absorption cross section.

  16. New supporting ligands in actinide chemistry: tetramethyltetraazaannulene complexes with thorium and uranium.

    Science.gov (United States)

    Hohloch, Stephan; Garner, Mary E; Parker, Bernard F; Arnold, John

    2017-10-17

    We report the synthesis, characterization, and preliminary reactivity of new heteroleptic thorium and uranium complexes supported by the macrocyclic TMTAA ligand (TMTAA = Tetramethyl-tetra-aza-annulene). The dihalide complexes Th(TMTAA)Cl2(THF)2 (1), [UCl2(TMTAA)]2 (2) and U(TMTAA)I2 (3) are further functionalized to the Cp* derivatives ThCp*(TMTAA)Cl (4), UCp*(TMTAA)Cl (5) and UCp*(TMTAA)I (6) (Cp* = pentamethylcyclopentadienide). Compounds 4-6 are also obtained through a one-pot reaction from standard thorium(iv) and uranium(iv) starting materials, Li2TMTAA and KCp*. Complexes 1-6 function as valuable starting materials for salt metathesis chemistry. Treatment of precursors 4 or 5 with trimethylsilylmethyllithium (LiCH2TMS) results in the new actinide TMTAA alkyl complexes ThCp*(TMTAA)(CH2TMS) (7) and UCp*(TMTAA)(CH2TMTS) (8), respectively. The TMTAA-derived alkyl complexes (7 and 8) show unexpected stability and are stable for several weeks at room temperature in solution and in the solid-state. Additionally, double substitution of the halide ligands in 1-3 shows a strong dependence on the nucleophile used. While weaker nucleophiles, such as amides, and more sterically demanding nucleophiles, such as Cp (Cp = cyclopenadienide), favour the formation of bis-TMTAA "sandwich" complexes [An(TMTAA)2] (An = Th (9) and An = U (10)), the use of oxygen-functionalized ligands like the ODipp anion (Dipp = diisopropylphenyl) results in the formation of the doubly substituted species Th(ODipp)2TMTAA (11) and U(ODipp)2TMTAA (12). We also describe the divergent reactivity of the TMTAA ligand towards uranium(iii). Unlike the syntheses of actinide(iv) TMTAA complexes, the synthesis of a uranium(iii) TMTAA was not successful and only uranium(iv) species could be obtained.

  17. The characterisation of a fulvic acid and its interactions with uranium and thorium

    Energy Technology Data Exchange (ETDEWEB)

    Davis, J.; Higgo, J.; Moore, Y.; Milne, C. [British Geological Survey, Nottingham (United Kingdom)

    1999-06-01

    The transport of actinides via colloids is very important to the production of a performance assessment for a nuclear waste repository e.g. Kersting et al. (1999). Organic colloids in the form of humic substances (HS) could constitute a major pathway for the migration of actinides away from the repository to the biosphere. The greater the stability of the actinide-HS complex the longer the potential migration pathway. BGS has continued with the laboratory experiments studying the interactions between U and Th and the Derwent Water-derived DE72 fulvic acid. DE72 FA has now been fully characterised, with data supplied for proton and copper binding titrations. Two different experimental methods have been developed to study complexation properties of actinides with DE72FA. Conditional stability constants have been derived for thorium binding to DE72 fulvic acid and these are comparable to literature data. Dissociation constants for thorium (IV) and the uranyl ion from DE72 FA have been obtained. After initial rapid dissociation the dissociation rates decrease to around 10{sup -5} min{sup -1}, for both uranium and thorium at pH between 6.5-7.4. The most important controlling parameter appears to be length of preconditioning time, or 'ageing' of solutions. (orig.)

  18. Uptake of uranium, thorium and radium isotopes by plants growing in dam impoundment Tasotkel and the Lower Shu region (Kazakhstan)

    Energy Technology Data Exchange (ETDEWEB)

    Matveyeva, Ilona; Burkitbayev, Mukhambetkali [al-Farabi Kazakh National University, Almaty (Kazakhstan). Faculty of Chemistry and Chemical Technology; Jacimovic, Radojko [Jozef Stefan Institute, Ljubljana (Slovenia). Dept. of Environmental Sciences; Planinsek, Petra; Smodis, Borut [Jozef Stefan Institute, Ljubljana (Slovenia). Dept. of Environmental Sciences; Jozef Stefan International Postgraduate School, Ljubljana (Slovenia)

    2016-04-01

    The activity concentrations of isotopes of uranium, thorium and radium-226 in dominant species of plants (Xantium strumarium, Phragmites communis, Artemisia nitrosa and Artemisia serotina) growing on the territories contaminated by uranium industry of Kazakhstan (close to dam impoundment Tasotkel and the Lower Shu region) are presented. The obtained data showed the significant variations of activity concentrations of isotopes of uranium, thorium and radium-226 in above ground parts. The concentrations of most of the investigated radionuclides in the root system are higher than in the aboveground parts; it can be explained by root barrier. It was found that the highest root barrier has Xantium strumarium, especially for uranium isotopes. The concentration ratios of radionuclides were calculated, and as the result it was found that the highest accumulation ability in the investigated region has Artemisia serotina.

  19. Uranium, thorium and rare earth elements distribution from different iron quadrangle spring waters

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Cláudia A.; Palmieri, Helena E.L.; Menezes, Maria A. de B.C.; Rodrigues, Paulo C.H., E-mail: cferreiraquimica@yahoo.com.br, E-mail: help@cdtn.br, E-mail: menezes@cdtn.br, E-mail: pchr@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2017-11-01

    This study was conducted to evaluate the concentrations of thorium, uranium and the rare earth elements (REE) in 26 spring waters, as well as the patterns of the REE of the samples from the Cercadinho, Moeda and Caue aquifers in different municipalities of the Iron Quadrangle (Quadrilatero Ferrifero), located in the central-southeast of Minas Gerais state. The pH value of the ground waters ranged from 3.8 to 7.0, indicating an acid nature of most of the spring waters. The investigation of REE speciation showed that all the REEs exist in the free X{sup 3+} ionic forms, under the prevailing Eh and pH conditions. In the studied samples the uranium concentrations (<2.3-1176 ng L{sup -1}) were below the guideline level set by Brazilian legislation (Ministry of Health 518- 03/2004). Thorium concentrations ranged from <0.39-11.0 ng L{sup -1} and the sum of the REE ranged from 6.0 to 37657 ng L{sup -1}. As there are no permissible limits related for the REE and thorium for different water quality standards in Brazil, more attention must be paid to the local residents' health risk caused by spring waters (REEs were > 1000 ng L{sup -1}) originating from aquifers located in Sabara, Barao de Cocais, Santa Barbara, Mario Campos, Congonhas and Lavras Novas. The REEs patterns in the spring waters from the Cercadinho, Caue and Moeda aquifers are characterized by middle REE (MREE) enrichment compared to light REE (LREE) and heavy REEs (HREE), negative Ce anomalies (except for one sample) and positive Eu anomalies in all three aquifers studied. (author)

  20. Optimization of thorium-uranium content in a 54-element fuel bundle for use in a CANDU-SCWR

    Energy Technology Data Exchange (ETDEWEB)

    Hummel, D.W.; Novog, D.R. [McMaster Univ., Dept. of Engineering Physics, Hamilton, Ontario (Canada)

    2011-07-01

    A new 54-element fuel bundle design has been proposed for use in a pressure-tube supercritical water-cooled reactor, a pre-conceptual evolution of existing CANDU reactors. Pursuant to the goals of the Generation IV International Forum regarding advancement in nuclear fuel cycles, optimization of the thorium and uranium content in each ring of fuel elements has been studied with the objectives of maximizing the achievable fuel utilization (burnup) and total thorium content within the bundle, while simultaneously minimizing the linear element ratings and coolant void reactivity. The bundle was modeled within a reactor lattice cell using WIMS-AECL, and the uranium and thorium content in each ring of fuel elements was optimized using a weighted merit function of the aforementioned criteria and a metaheuristic search algorithm. (author)

  1. Actinide Corroles: Synthesis and Characterization of Thorium(IV) and Uranium(IV) bis(-chloride) Dimers

    Energy Technology Data Exchange (ETDEWEB)

    Ward, Ashleigh L.; Buckley, Heather L.; Gryko, Daniel T.; Lukens, Wayne W.; Arnold, John

    2013-12-01

    The first synthesis and structural characterization of actinide corroles is presented. Thorium(IV) and uranium(IV) macrocycles of Mes2(p-OMePh)corrole were synthesised and characterized by single-crystal X-ray diffraction, UV-Visible spectroscopy, variable-temperature 1H NMR, ESI mass spectrometry and cyclic voltammetry.

  2. Uranium and thorium based phosphate matrix: synthesis, characterizations and lixiviation; Matrices a base de phosphate d'uranium et de thorium: syntheses, caracterisations et lixiviation

    Energy Technology Data Exchange (ETDEWEB)

    Dacheux, N

    1995-03-01

    In the framework of the search for a ceramic material usable in the radioactive waste storage, uranium and thorium phosphates have been investigated. Their experimental synthesis conditions have been entirely reviewed, they lead to the preparation of four new compounds: U(UO{sub 2})(PO{sub 4}){sub 2}, U{sub 2}O(PO{sub 4}){sub 2}, UCIPO{sub 4}, 4H{sub 2}O, and Th{sub 4}(PO{sub 4}){sub 4}P{sub 2}O{sub 7}. Experimental evidenced are advanced for non existent compounds such as: U{sub 3}(PO{sub 4}){sub 4}, U{sub 2}O{sub 3}P{sub 2}O{sub 7} and Th{sub 3} (PO{sub 4}){sub 4}. Characterization by several techniques (X-rays and neutron powder diffractions, UV-Visible and Infra-red spectroscopies, XPS,...) were performed. The ab initio structure determination of U(UO{sub 2})(PO{sub 4}){sub 2} has been achieved by X-rays and refined by neutron diffractions. Through its physico-chemical analysis, we found that this compound was a new mixed valence uranium phosphate in which U{sup 4+} and UO{sub 2}{sup 2+} ions are ordered in pairs along parallel chains according to a new type of arrangement. Reaction mechanism, starting from UCIPO{sub 4}, 4H{sub 2}O and based on redox processes of uranium in solid state was set up. From two main matrices U(UO{sub 2})(PO{sub 4}){sub 2} and Th{sub 4}(PO{sub 4}){sub 4}P{sub 2}O{sub 7}, solid solutions were studied. They consist of replacement of U(IV) by Th(IV) and reversely. The leaching tests on pure, loaded and doped matrices were performed in terms of storage time, pH of solutions, and determined by the use of solids labelled with {sup 230}U or by the measurement of uranyl concentration by Laser-Induced Time-Resolved Spectro-fluorimetry. Average concentration of uranium in the liquid phase is around 10{sup -4} M to 10{sup -6} M. Taking into account the very low solubilities of the studied phosphate ceramics, we estimated their chemical performances promising as an answer to the important nuclear waste problem, if we compare them to the glasses

  3. Contribution to the geochemical knowledge of the uranium-radium and thorium families in the southern Vosges. Applications of some results in the prospecting of uranium deposits; Contribution a la connaissance geochimique des familles uranium-radium et du thorium dans les Vosges meridionales. Application de certains resultats en prospection des gisements d'uranium

    Energy Technology Data Exchange (ETDEWEB)

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

    1962-07-01

    This work's aim is to lead to a more accurate knowledge of the geochemistry of the Uranium-Radium and Thorium families in the Southern Vosges and to apply some of the results to the prospecting of uraniferous deposits: It has been showed: a bond between Calcium-Magnesium and Uranium-Thorium in the calco-alkaline granites. The host minerals of Uranium and Thorium are hornblende, biotite, titanite and epidote. a concentration of Uranium, at present time with secular disequilibrium in a thermal zone where the satellite mineralizations form an epithermal paragenesis. a disequilibrium of the Uranium-Radium family in the supergene minerals of the lead (phosphate and vanadate) showing the present circulations of Uranium. a bond between the radon grade of the spring waters and Uranium-Radium of the rocks. Such a relation allow to realize a prospecting method based on the determination of radioactive gases from the cold spring-waters of a common country. (author) [French] L'etude presentee ici a pour but de conduire a une connaissance plus precise de la geochimie des familles Uranium-Radium et Thorium dans les Vosges meridionales et d'appliquer certains resultats a la prospection des gites uraniferes. Il a ete mis en evidence: une liaison Calcium-Magnesium et Uranium-Thorium dans des granites calco-alcalins. Les mineraux hotes de l'Uranium et du Thorium sont: la hornblende, la biotite, le sphene, l'epidote. une concentration actuelle de l'Uranium en desequilibre seculaire dans une zone thermale ou les mineralisations satellites constituent une paragenese epithermale. un desequilibre de la famille Uranium-Radium dans des mineraux supergenes du plomb (phosphates et vanadates) prouvant les circulations actuelles de l'Uranium. une liaison entre la teneur en Radon des eaux de sources et celle en Uranium-Radium des roches. Une telle liaison permet de realiser une methode de prospection fondee sur le dosage du gaz radioactif des eaux de sources

  4. 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.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1991-06-01

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

  6. Sorption and coprecipitation of trace concentrations of thorium with various minerals under conditions simulating an acid uranium mill effluent environment

    Science.gov (United States)

    Landa, Edward R.; Le, Anh H.; Luck, Rudy L.; Yeich, Philip J.

    1995-01-01

    Sorption of thorium by pre-existing crystals of anglesite (PbSO4), apatite (Ca5(PO4)3(HO)), barite (BaSO4), bentonite (Na0.7Al3.3Mg0.7Si8O20(OH)4), celestite (SrSO4), fluorite (CaF2), galena (PbS), gypsum (CaSO4·2H2O), hematite (Fe2O3), jarosite (KFe3(SO4)2(OH)6), kaolinite (Al2O3·2SiO2·2H2O), quartz (SiO2) and sodium feldspar (NaAlSi3O8) was studied under conditions that simulate an acidic uranium mill effluent environment. Up to 100% removal of trace quantitiees of thorim (approx. 1.00 ppm in 0.01 N H2SO4) from solution occurred within 3 h with fluorite and within 48 h in the case of bentonite. Quartz, jarosite, hematite, sodium feldspar, gypsum and galena removed less than 15% of the thorium from solution. In the coprecipitation studies, barite, anglesite, gypsum and celestite were formed in the presence of thorium (approx. 1.00 ppm). Approximately all of the thorium present in solution coprecipitated with barite and celestite; 95% coprecipitated with anglesite and less than 5% with gypsum under similar conditions. When jarosite was precipitated in the presence of thorium, a significant amount of thorium (78%) was incorporated in the precipitate.

  7. Feasibility study on AFR-100 fuel conversion from uranium-based fuel to thorium-based fuel

    Energy Technology Data Exchange (ETDEWEB)

    Heidet, F.; Kim, T.; Grandy, C. (Nuclear Engineering Division)

    2012-07-30

    Although thorium has long been considered as an alternative to uranium-based fuels, most of the reactors built to-date have been fueled with uranium-based fuel with the exception of a few reactors. The decision to use uranium-based fuels was initially made based on the technology maturity compared to thorium-based fuels. As a result of this experience, lot of knowledge and data have been accumulated for uranium-based fuels that made it the predominant nuclear fuel type for extant nuclear power. However, following the recent concerns about the extent and availability of uranium resources, thorium-based fuels have regained significant interest worldwide. Thorium is more abundant than uranium and can be readily exploited in many countries and thus is now seen as a possible alternative. As thorium-based fuel technologies mature, fuel conversion from uranium to thorium is expected to become a major interest in both thermal and fast reactors. In this study the feasibility of fuel conversion in a fast reactor is assessed and several possible approaches are proposed. The analyses are performed using the Advanced Fast Reactor (AFR-100) design, a fast reactor core concept recently developed by ANL. The AFR-100 is a small 100 MW{sub e} reactor developed under the US-DOE program relying on innovative fast reactor technologies and advanced structural and cladding materials. It was designed to be inherently safe and offers sufficient margins with respect to the fuel melting temperature and the fuel-cladding eutectic temperature when using U-10Zr binary metal fuel. Thorium-based metal fuel was preferred to other thorium fuel forms because of its higher heavy metal density and it does not need to be alloyed with zirconium to reduce its radiation swelling. The various approaches explored cover the use of pure thorium fuel as well as the use of thorium mixed with transuranics (TRU). Sensitivity studies were performed for the different scenarios envisioned in order to determine the

  8. Aqueous biphasic extraction of uranium and thorium from contaminated soils. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Chaiko, D.J.; Gartelmann, J.; Henriksen, J.L.; Krause, T.R.; Deepak; Vojta, Y.; Thuillet, E.; Mertz, C.J.

    1995-07-01

    The aqueous biphasic extraction (ABE) process for soil decontamination involves the selective partitioning of solutes and fine particulates between two immiscible aqueous phases. The biphase system is generated by the appropriate combination of a water-soluble polymer (e.g., polyethlene glycol) with an inorganic salt (e.g., sodium carbonate). Selective partitioning results in 99 to 99.5% of the soil being recovered in the cleaned-soil fraction, while only 0.5 to 1% is recovered in the contaminant concentrate. The ABE process is best suited to the recovery of ultrafine, refractory material from the silt and clay fractions of soils. During continuous countercurrent extraction tests with soil samples from the Fernald Environmental Management Project site (Fernald, OH), particulate thorium was extracted and concentrated between 6- and 16-fold, while the uranium concentration was reduced from about 500 mg/kg to about 77 mg/kg. Carbonate leaching alone was able to reduce the uranium concentration only to 146 mg/kg. Preliminary estimates for treatment costs are approximately $160 per ton of dry soil. A detailed flowsheet of the ABE process is provided.

  9. Criticality analysis for mixed thorium-uranium fuel in the Angra-2 PWR reactor using KENO-VI

    Energy Technology Data Exchange (ETDEWEB)

    Wichrowski, Caio C.; Gonçalves, Isadora C.; Oliveira, Claudio L.; Vellozo, Sergio O.; Baptista, Camila O., E-mail: wichrowski@ime.eb.br, E-mail: isadora.goncalves@ime.eb.br, E-mail: d7luiz@yahoo.com.br, E-mail: vellozo@ime.eb.br, E-mail: camila.oliv.baptista@gmail.com [Instituto Militar de Engenharia (IME), Rio de Janeiro, RJ (Brazil). Seção de Engenharia Nuclear

    2017-07-01

    The increasing energy demand associated to the current sustainability challenges have given the thorium nuclear fuel cycle renewed interest in the scientific community. Studies have focused on energy production in different reactor designs through the fission of uranium 233, the product of thorium fertilization by neutrons. In order to make it possible for near future applications a strategy based on the adaptation of current nuclear reactors for the use of thorium fuels is being considered. In this work, bearing in mind these limitations, a code was used to evaluate the effect on criticality (k{sub inf}) of the mixing of thorium and uranium in different proportions in the fuel of a PWR, the German designed Angra-2 Brazilian reactor in order to scrutinise its behaviour and determine the feasibility of an adapted ThO{sub 2}-UO{sub 2} mixed fuel cycle using current PWR technology. The analysis is performed using the KENO-VI module in the SCALE 6.1 nuclear safety analysis simulation code and the information is taken from the Angra-2 FSAR (Final Security Analysis Report). (author)

  10. Environmental releases from fuel cycle facility: part 1: radionuclide resuspension vs. stack releases on ambient airborne uranium and thorium levels.

    Science.gov (United States)

    Masson, Olivier; Pourcelot, Laurent; Boulet, Béatrice; Cagnat, Xavier; Videau, Gérard

    2015-03-01

    Airborne activity levels of uranium and thorium series were measured in the vicinity (1.1 km) of a uranium (UF4) processing plant, located in Malvési, south of France. Regarding its impact on the environment, this facility is characterized by its routine atmospheric releases of uranium and by the emission of radionuclide-labelled particles from a storage pond filled with waste water or that contain dried sludge characterized by traces of plutonium and thorium ((230)Th). This study was performed during a whole year (November 2009-November 2010) and based on weekly aerosol sampling. Thanks to ICP-MS results, it was possible to perform investigations of uranium and thorium decay product concentration in the air. The number of aerosol filters sampled (50) was sufficient to establish a relationship between airborne radionuclide variations and the wind conditions. As expected, the more the time spent in the plume, the higher the ambient levels. The respective contributions of atmospheric releases and resuspension from local soil and waste ponds on ambient dust load and uranium-bearing aerosols were estimated. Two shutdown periods dedicated to facility servicing made it possible to estimate the resuspension contribution and to specify its origin (local or regional) according to the wind direction and remote background concentration. Airborne uranium mainly comes from the emission stack and, to a minor extent (∼20%), from wind resuspension of soil particles from the surrounding fields and areas devoted to waste storage. Moreover, weighed activity levels were clearly higher during operational periods than for shutdown periods. Copyright © 2014 Elsevier Ltd. All rights reserved.

  11. Different periods of uranium and thorium occurrence in Madagascar (1960); Cycles uraniferes et thoriferes a Madagascar (1960)

    Energy Technology Data Exchange (ETDEWEB)

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

    1960-07-01

    In Madagascar, the first typical occurrences of thorium and uranium are about 500 million years old. Previously thorium and uranium were rather concentrated in the granitic and charnockitic zones, chiefly in minerals such as monazite, apatite and zircon. At the end of the Precambrian period, metasomatic granites occur especially in the anticlinal series (Andriba orthite granite). The granitization is followed by the formation of the main pegmatitic areas in the Island with Th-U niobotantalates, uraninite and beryl. The pegmatites are well developed in the synclinal series with a poor migmatization or no migmatization at all. In the same time a large uranium and thorium province with uranothorianite deposits appears within the calcomagnesian series of the Southern part of Madagascar. Later, large amounts of monazite were carried down to the detritic Karroo sediments during tile erosion of the metamorphic precambrian rocks. Monazite has been concentrated again by frequent marine incursions, till the present time. In the medium Karroo, near Folakara, uranium minerals occur in direct relation with carbonaceous material. Finally we must note the uranium occurrence in the pleistocene carbonaceous shales of Antsirabe basin, in contact with crystalline rocks. (author) [French] A Madagascar, le premier cycle uranifere et thorifere bien caracterise se situe aux alentours de 500 millions d'annees. Auparavant, le thorium et l'uranium sont concentres de preference dans les zones granitiques et charnockites sous forme de monazite, apatite ou zircon. Vers la fin du Precambrien, se produisent des granitisations metasomatiques, surtout dans les zones anticlinales (type Andriba a orthite). La fin de cette granitisation s'accompagne de la formation des principaux champs pegmatitiques de l'Ile a niobotantalates uraniferes, uraninite et beryl, qui se developpent de preference dans les series synclinales peu ou pas migmatisees. A cette meme epoque s

  12. Dissolution study of thorium-uranium oxides in aqueous triflic acid solutions

    Energy Technology Data Exchange (ETDEWEB)

    Bulemela, E.; Bergeron, A.; Stoddard, T. [Canadian Nuclear Laboratories - CNL, 286 Plant Rd., Chalk River, Ontario, K0J 1J0 (Canada)

    2016-07-01

    The dissolution of sintered mixed oxides of thorium with uranium in various concentrations of trifluoromethanesulfonic (triflic) acid solutions was investigated under reflux conditions to evaluate the suitability of the method. Various fragment sizes (1.00 mm < x < 7.30 mm) of sintered (Th,U)O{sub 2} and simulated high-burnup nuclear fuel (SIMFUEL) were almost completely dissolved in a few hours, which implies that triflic acid could be used as an alternative to the common dissolution method, involving nitric acid-hydrofluoric acid mixture. The influence of acid concentration, composition of the solids, and reaction time on the dissolution yield of Th and U ions was studied using Inductively Coupled Plasma - Mass Spectrometry (ICP-MS). The dissolution rate was found to depend upon the triflic acid concentration and size of the solid fragments, with near complete dissolution for the smallest fragments occurring in boiling 87% w/w triflic acid. The formation of Th and U ions in solution appears to occur at the same rate as the triflic acid simultaneously reacts with the constituent oxides as evidenced by the results of a constant U/Th concentration ratio with the progress of the dissolution. (authors)

  13. Assessment of the bioavailability and depuration of uranium, cesium and thorium in snails (Cantareus aspersus) using kinetics models

    Energy Technology Data Exchange (ETDEWEB)

    Pauget, B., E-mail: benjamin.pauget@tesora.fr [Tésora, Le Visium, 22 Av. Aristide Briand, 94110 Arcueil (France); Andra, R& D Division, Centre de Meuse/Haute-Marne, RD 960, 55290 Bure (France); University of Bourgogne Franche-Comté, Department Chrono-Environnement, UMR UFC/CNRS 6249, 16 Route de Gray, 25030 Besançon Cedex (France); Villeneuve, A.; Redon, P.O. [Tésora, Le Visium, 22 Av. Aristide Briand, 94110 Arcueil (France); Cuvier, A. [ECOLAB, Université de Toulouse, CNRS, INPT, UPS, Toulouse (France); IRSN/PRP-ENV/SESURE/Laboratoire d’études radioécologiques en milieu continental et marin, BP 1, 13108 Saint-Paul-lès-Durance Cedex (France); Vaufleury, A. de [University of Bourgogne Franche-Comté, Department Chrono-Environnement, UMR UFC/CNRS 6249, 16 Route de Gray, 25030 Besançon Cedex (France)

    2017-08-05

    Highlights: • Kinetic studies allow to take into account the dynamic mechanisms of bioavailability. • An absence of Cs and Th accumulation is evidenced showing their low bioavailability. • The uranium accumulation is not only a function of the soil contamination. - Abstract: Uranium ore waste has led to soil contamination that may affect both environmental and soil health. To analyze the risk of metal transfer, metal bioavailability must be estimated by measuring biological parameters. Kinetic studies allow taking into account the dynamic mechanisms of bioavailability, as well as the steady state concentration in organisms necessary to take into account for relevant risk assessment. In this way, this work aims to model the snail accumulation and excretion kinetics of uranium (U), cesium (Cs) and thorium (Th). Results indicate an absence of Cs and Th accumulation showing the low bioavailability of these two elements and a strong uranium accumulation in snails related to the levels of soil contamination. During the depuration phase, most of the uranium ingested was excreted by the snails. After removing the source of uranium by soil remediation, continued snails excretion of accumulated uranium would lead to the return of their initial internal concentration, thus the potential trophic transfer of this hazardous element would stop.

  14. Functional Sorbents for Selective Capture of Plutonium, Americium, Uranium, and Thorium in Blood

    Science.gov (United States)

    Yantasee, Wassana; Sangvanich, Thanapon; Creim, Jeffery A; Pattamakomsan, Kanda; Wiacek, Robert J; Fryxell, Glen E; Addleman, R Shane; Timchalk, Charles

    2010-01-01

    Self-assembled monolayer on mesoporous supports (SAMMS™) are hybrid materials created from attachment of organic moieties onto very high surface area mesoporous silica. SAMMS with surface chemistries including three isomers of hydroxypyridinone, diphosphonic acid, acetamide phosphonic acid, glycinyl urea, and diethylenetriamine pentaacetate (DTPA) analog were evaluated for chelation of actinides (239Pu, 241Am, uranium, thorium) from blood. Direct blood decorporation using sorbents does not have toxicity or renal challenges associated with traditional chelation therapy and may have potential applications for critical exposure cases, reduction of nonspecific dose during actinide radiotherapy, and for sorbent hemoperfusion in renal insufficient patients, whose kidney clear radionuclides at very slow rate. Sorption affinity (Kd), sorption rate, selectivity, and stability of SAMMS were measured in batch contact experiments. An isomer of hydroxypyridinone (3,4-HOPO) on SAMMS demonstrated the highest affinity for all four actinides from blood and plasma and greatly outperformed the DTPA analog on SAMMS and commercial resins. In batch contact, a fifty percent reduction of actinides in blood was achieved within minutes, and there was no evidence of protein fouling or material leaching in blood after 24 hr. The engineered form of SAMMS (bead format) was further evaluated in a 100-fold scaled-down hemoperfusion device and showed no blood clotting after 2 hr. A 0.2 g quantity of SAMMS could reduce 50 wt.% of 100 ppb uranium in 50 mL of plasma in 18 min and that of 500 dpm mL−1 in 24 min. 3,4-HOPO-SAMMS has a long shelf-life in air and at room temperature for at least 8 years, indicating its feasibility for stockpiling in preparedness for an emergency. The excellent efficacy and stability of SAMMS materials in complex biological matrices suggest that SAMMS can also be used as orally administered drugs and for wound decontamination. By changing the organic groups of SAMMS

  15. Functional sorbents for selective capture of plutonium, americium, uranium, and thorium in blood.

    Science.gov (United States)

    Yantasee, Wassana; Sangvanich, Thanapon; Creim, Jeffery A; Pattamakomsan, Kanda; Wiacek, Robert J; Fryxell, Glen E; Addleman, R Shane; Timchalk, Charles

    2010-09-01

    Self-assembled monolayer on mesoporous supports (SAMMS) are hybrid materials created from attachment of organic moieties onto very high surface area mesoporous silica. SAMMS with surface chemistries including three isomers of hydroxypyridinone, diphosphonic acid, acetamide phosphonic acid, glycinyl urea, and diethylenetriamine pentaacetate (DTPA) analog were evaluated for chelation of actinides ((239)Pu, (241)Am, uranium, thorium) from blood. Direct blood decorporation using sorbents does not have the toxicity or renal challenges associated with traditional chelation therapy and may have potential applications for critical exposure cases, reduction of nonspecific dose during actinide radiotherapy, and for sorbent hemoperfusion in renal insufficient patients, whose kidneys clear radionuclides at a very slow rate. Sorption affinity (K(d)), sorption rate, selectivity, and stability of SAMMS were measured in batch contact experiments. An isomer of hydroxypyridinone (3,4-HOPO) on SAMMS demonstrated the highest affinity for all four actinides from blood and plasma and greatly outperformed the DTPA analog on SAMMS and commercial resins. In batch contact, a fifty percent reduction of actinides in blood was achieved within minutes, and there was no evidence of protein fouling or material leaching in blood after 24 h. The engineered form of SAMMS (bead format) was further evaluated in a 100-fold scaled-down hemoperfusion device and showed no blood clotting after 2 h. A 0.2 g quantity of SAMMS could reduce 50 wt.% of 100 ppb uranium in 50 mL of plasma in 18 min and that of 500 dpm mL(-1) in 24 min. 3,4-HOPO-SAMMS has a long shelf-life in air and at room temperature for at least 8 y, indicating its feasibility for stockpiling in preparedness for an emergency. The excellent efficacy and stability of SAMMS materials in complex biological matrices suggest that SAMMS can also be used as orally administered drugs and for wound decontamination. By changing the organic groups of

  16. Uranium and thorium series disequilibrium in quaternary carbonate deposits from the Serra da Bodoquena and Pantanal do Miranda, Mato Grosso do Sul State, central Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Ribeiro, Fernando Brenha E-mail: brenha@iag.usp.br; Roque, Arnaldo; Boggiani, Paulo Cesar; Flexor, J.-M

    2001-01-15

    Activities of gamma-ray emitting members of the uranium ({sup 238}U) and thorium ({sup 232}Th) series were measured in a quaternary limestone deposit that outcrops in the southeastern Pantanal Matogrossense Basin and in quaternary tufas deposited at the drainage of the Serra da Bodoquena. It is a first step in a study of the mobilization of uranium and thorium series and its relation to surface hydrology, in a region where carbonate deposits are being continuously dissolved and reprecipitated. The obtained results show that all these deposits are characterized by very low concentrations of uranium and thorium. The {sup 238}U/{sup 226}Ra and {sup 228}Th/{sup 228}Ra activity ratios are significantly different than 1.0, indicating that both series are in radioactive disequilibrium. Although the Serra da Bodoquena deposits seem to be very recent, their very fine granulation and high porosity suggest that they behave as open systems for geochemical exchanges of uranium and thorium series members. The Pantanal do Miranda limestone has a radiocarbon age of 3900 yr BP. Since the thorium series is in disequilibrium it is also concluded that this deposit behaves as an open system for geochemical exchanges.

  17. Adsorption of uranium and thorium on new adsorbent prepared from Moroccan oil shale impregnated with phosphoric acid

    OpenAIRE

    El Hassane Khouya; Khadija Legrouri; Said Fakhi; Hassan Hannache

    2010-01-01

    Attention has been focused recently on the production of new adsorbents from Moroccan oil shale of Tarfaya (layer R3) by chemical activation with phosphoric acid and its application in wastewaters treatment. The optimal conditions for the preparation were searched and the tests of adsorption of uranium and thorium ions were affected. The best product was obtained by used of the ratio of activated agent/precursor equal 3 and activation of the mixture in air at 250°C during two hours after...

  18. Elemental bio-imaging of thorium, uranium, and plutonium in tissues from occupationally exposed former nuclear workers.

    Science.gov (United States)

    Hare, Dominic; Tolmachev, Sergei; James, Anthony; Bishop, David; Austin, Christine; Fryer, Fred; Doble, Philip

    2010-04-15

    Internal exposure from naturally occurring radionuclides (including the inhaled long-lived actinides (232)Th and (238)U) is a component of the ubiquitous background radiation dose (National Council on Radiation Protection and Measurements. Ionizing radiation exposure of the population of the United States; NCRP Report No. 160; NCRP: Bethesda, MD, 2009). It is of interest to compare the concentration distribution of these natural alpha-emitters in the lungs and respiratory lymph nodes with those resulting from occupational exposure, including exposure to anthropogenic plutonium and depleted and enriched uranium. This study examines the application of laser ablation-inductively coupled plasma-mass spectrometry (LA-ICPMS) to quantifying and visualizing the mass distribution of uranium and thorium isotopes from both occupational and natural background exposure in human respiratory tissues and, for the first time, extends this application to the direct imaging of plutonium isotopes. Sections of lymphatic and lung tissues taken from deceased former nuclear workers with a known history of occupational exposure to specific actinide elements (uranium, plutonium, or americium) were analyzed by LA-ICPMS. Using a previously developed LA-ICPMS protocol for elemental bio-imaging of trace elements in human tissue and a new software tool, we generated images of thorium ((232)Th), uranium ((235)U and (238)U), and plutonium ((239)Pu and (240)Pu) mass distributions in sections of tissue. We used a laboratory-produced matrix-matched standard to quantify the (232)Th, (235)U, and (238)U concentrations. The plutonium isotopes (239)Pu and (240)Pu were detected by LA-ICPMS in 65 mum diameter localized regions of both a paratracheal lymph node and a sample of lung tissue from a person who was occupationally exposed to refractory plutonium (plutonium dioxide). The average (overall) (239)Pu concentration in the lymph node was 39.2 ng/g, measured by high purity germanium (HPGe) gamma

  19. Standard test method for analysis of uranium and thorium in soils by energy dispersive X-Ray fluorescence spectroscopy

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2011-01-01

    1.1 This test method covers the energy dispersive X-ray fluorescence (EDXRF) spectrochemical analysis of trace levels of uranium and thorium in soils. Any sample matrix that differs from the general ground soil composition used for calibration (that is, fertilizer or a sample of mostly rock) would have to be calibrated separately to determine the effect of the different matrix composition. 1.2 The analysis is performed after an initial drying and grinding of the sample, and the results are reported on a dry basis. The sample preparation technique used incorporates into the sample any rocks and organic material present in the soil. This test method of sample preparation differs from other techniques that involve tumbling and sieving the sample. 1.3 Linear calibration is performed over a concentration range from 20 to 1000 μg per gram for uranium and thorium. 1.4 The values stated in SI units are to be regarded as the standard. The inch-pound units in parentheses are for information only. 1.5 This standard...

  20. Uranium and thorium nuclides series determined in medicinal plants commonly used in Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Silva, P.; Francisconi, L.; Damatto, S. [IPEN/CNEN-SP, Sao Paulo (Brazil)

    2014-07-01

    In recent years the study of medicinal plants has become the focus of ever more extensive research all over the world due to their diversity and potential as source of medicinal products. According to the World Health Organization approximately 80% of world population makes use of medicinal herbs due to their believed therapeutic action. Besides being used as medicine, medicinal plants are also largely used as dietary supplements. The presence of radionuclides in plants constitutes one of the main pathways for their transfer to man. The amount of radioactive nuclides from U and Th series in edible vegetables are relatively well known since they have been the main concern of research conducted worldwide. Medicinal plants, on the other hand, have been neglected in these studies, possibly because the ingestion of radioactive material through their consumption has not been recognized or was considered insignificant. The objective of the present study was to determine the content of natural radionuclides from {sup 238}U and {sup 232}Th series in 25 species of medicinal plants used in Brazil, both as medicine and as dietary supplement. The medicinal plant samples were obtained in specialized pharmacies and drugstores. The raw plant and their extracts, produced as recommended by the National Agency for Sanitary Vigilance, were analyzed by Instrumental Neutron Activation Analyses for the determination of U and Th and by Total Alpha and Beta Counting after Radiochemical Separation for determination of {sup 226}Ra, {sup 228}Ra and {sup 210}Pb. In the raw plants the activity concentrations varied from 0,08 Bq kg{sup -1} to 8,0 Bq kg{sup -1} for thorium, from < LID to 22 Bq kg{sup -1} for uranium, from 1,8 Bq kg{sup -1} to 12 Bq kg{sup -1} for {sup 226}Ra, from 33 Bq kg{sup -1} to 74 Bq kg{sup -1} for {sup 228}Ra and from 10 Bq kg{sup -1} to 120 Bq kg{sup -1} for {sup 210}Pb. In the extracts, the activity concentrations varied from 9 mBq kg{sup -1} to 137 mBq kg{sup -1} for Th

  1. Fluor determination by alkaline hydrolysis of the uranium and thorium fluorides; Determinacion de fluor por hidrolisis alcalina en fluoruros de uranio y torio

    Energy Technology Data Exchange (ETDEWEB)

    Barrachina Gomez, L.; Gasco Sanchez, L.

    1961-07-01

    The alkaline hydrolysis of the uranium and thorium fluorides is studded and a new method for the determination of the fluoride, on the basis of a indirect volumetric titration with standard soda, is proposed. The compounds that may influence the hydrolysis of the uranium fluoride and that may be occasionally found in it as impurities are also studied. the method can be applied to the uranium fluoride except when there is a great quantity of F{sub 2}UO{sub 2} or UO{sub 3} present in the sample. (Author) 20 refs.

  2. Uptake of radionuclide thorium by twelve native plants grown in uranium mill tailings soils from south part of China

    Energy Technology Data Exchange (ETDEWEB)

    Yan, Xun, E-mail: m13836295186@163.com

    2016-08-01

    Highlights: • Screen dominant plants grown in uranium mill tailings soils. • Quantify the content of {sup 232}Th of soil samples from uranium mill tailings. • Quantify the transfer factor, bioconcentration factor and phytoremediation factor. • Screen out the plant species capable of remediating radionuclide contaminated soils. • Guide the reuse of study area in future. - Abstract: The concentrations of thorium ({sup 232}Th) in soil from a uranium mill tailings repository in South China were analyzed. The results showed that all the soil samples were acidic and the concentrations of {sup 232}Th in all the soil samples were more than the natural radionuclide content in soil of China. Through the field investigation, twelve kinds of dominant plants were discovered. The total quantity of {sup 232}Th in the whole plant is highest in rice flat sedge. We also found that Miscanthus floridulus has the greatest transfer factor (TF) for {sup 232}Th, rice flat sedge has the greatest bioconcentration factor (BF) for {sup 232}Th. At the mean time, M. floridulus has the greatest phytoremediation factor (PF) for {sup 232}Th. On the basis of the above conclusions and the definition for hyperaccumulator, rice flat sedge and M. floridulus could be the candidates of phytoremediation for radionuclide {sup 232}Th in the soil.

  3. Potentialities and practical limitations of absolute neutron dosimetry using thin films of uranium and thorium applied to the fission track dating

    CERN Document Server

    Bigazzi, G; Hadler-Neto, J C; Iunes, P J; Paulo, S R; Oddone, M; Osorio, A M A; Zúñiga, A G

    1999-01-01

    Neutron dosimetry using natural uranium and thorium thin films makes possible that mineral dating by the fission-track method can be accomplished, even when poor thermalized neutron facilities are employed. In this case, the contributions of the fissions of sup 2 sup 3 sup 5 U, sup 2 sup 3 sup 8 U and sup 2 sup 3 sup 2 Th induced by thermal, epithermal and fast neutrons to the population of tracks produced during irradiation are quantified through the combined use of natural uranium and thorium films. If the Th/U ratio of the sample is known, only one irradiation (where the sample and the films of uranium and thorium are present) is necessary to perform the dating. However, if that ratio is unknown, it can be determined through another irradiation where the mineral to be dated and both films are placed inside a cadmium box. Problems related with film manufacturing and calibration are discussed. Special attention is given to the utilization of thin films having very low uranium content. The problems faced sugg...

  4. Uranium, thorium, gross alpha and gross beta assessment in fountain waters in towns of the Iron Quadrangle, Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira, Claudia A.; Palmieri, Helena E.L.; Menezes, Maria Angela de B.C.; Chaves, Renata D.A.; Dalmazio, Ilza, E-mail: cferreiraquimica@yahoo.com.br, E-mail: help@cdtn.br, E-mail: menezes@cdtn.br, E-mail: rda@cdtn.br, E-mail: id@cdtn.br [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil)

    2013-07-01

    The Iron Quadrangle region is known worldwide for its diversity, both ores and rock types, which record a long and important period of Earth's history. For thousands of years erosive processes have exposed ancient rocks, Archean and Proterozoic, in this region. The concentration of uranium, thorium, gross alpha and gross beta activities has been assessed in 34 fountains water samples collected from different towns in the Iron Quadrangle. The results obtained were compared to values established by CONAMA nº 396/2008 and Decree nº 2914/2011 by the Ministry of Health. For Th in water consumption there is no value established in the Brazilian legislation and the concentrations in all samples were lower than 0.01 μg L{sup -1}. For uranium, the values ranged from less than 0.002 to 0.61 μg L{sup -1}, and all results were lower than the value allowed of 15 μg L{sup -1} and 30 μg L{sup -1} established by the legislations above, respectively. The results for the radiation levels of gross alpha and gross beta activity in some fountains waters were slightly above the limits (0.5 Bq L{sup -1} and 1.0 Bq L{sup -1}) established by CONAMA nº 396/2008 and Decreet nº 2914/2011, respectively. (author)

  5. Dioxins, furans, biphenyls, arsenic, thorium and uranium in natural and anthropogenic sources of phosphorus and calcium used in agriculture.

    Science.gov (United States)

    Avelar, A C; Ferreira, W M; Pemberthy, D; Abad, E; Amaral, M A

    2016-05-01

    The aim of this study was to assess the presence of dioxins, furans and biphenyls, and the inorganic contaminants such as arsenic (As), thorium (Th) and uranium (U) in three main products used in Agriculture in Brazil: feed grade dicalcium phosphate, calcined bovine bone meal and calcitic limestone. The first two are anthropogenic sources of phosphorus and calcium, while calcitic limestone is a natural unprocessed mineral. Regarding to dioxin-like substances, all samples analyzed exhibited dioxins (PCDD) and furans (PCDF) and dioxin-like polychlorinated biphenyls (dl-PCBs) concentrations below limit of detection (LOD). In general, achieved is in accordance with regulation in Brazil where is established a maximum limit in limestone used in the citric pulp production (0.50pg WHO-TEQ g(-1)). In addition, reported data revealed very low levels for limestone in comparison with similar materials reported by European legislation. As result for toxic metals, achieved data were obtained using Instrumental Neutron Activation Analysis (INAA). On one hand, limestone sample exhibits the largest arsenic concentration. On another hand, dicalcium phosphate exhibited the largest uranium concentration, which represents a standard in animal nutrition. Therefore, it is phosphorus source in the animal feed industry can be a goal of concern in the feed field. Copyright © 2016 Elsevier B.V. All rights reserved.

  6. Further insight into uranium and thorium metaphosphate chemistry and the effect of Nd{sup 3+} incorporation into uranium(IV) metaphosphate

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Na; Neumeier, Stefan; Bosbach, Dirk [Forschungszentrum Juelich GmbH, Institute of Energy and Climate Research (IEK-6), Juelich (Germany); Klepov, Vladislav V. [Forschungszentrum Juelich GmbH, Institute of Energy and Climate Research (IEK-6), Juelich (Germany); Department of Chemistry, Samara State University (Russian Federation); Depmeier, Wulf [Institute of Geosciences, University of Kiel (Germany); Suleimanov, Evgeny V. [Department of Chemistry, Lobachevsky State University of Nizhny Novgorod (Russian Federation); Alekseev, Evgeny V. [Forschungszentrum Juelich GmbH, Institute of Energy and Climate Research (IEK-6), Juelich (Germany); Institut fuer Kristallographie, RWTH Aachen University, (Germany)

    2015-03-15

    A tetragonal modification of uranium polymetaphosphate U(PO{sub 3}){sub 4}, a mixed U{sup 4+}/Nd{sup 3+} polymetaphosphate ''(U{sub 0.62}Nd{sub 0.38})(PO{sub 3}){sub 4}'', and two new tetraphosphates, Th(P{sub 4}O{sub 12}) and U(P{sub 4}O{sub 12}), were synthesized. The structures of the obtained materials were characterized by X-ray diffraction and Raman spectroscopy. The presence of Nd in (U{sub 0.62}Nd{sub 0.38})(PO{sub 3}){sub 4} was proven by energy-dispersive X-ray spectroscopy (EDX), and the measured degree of substitution for U agrees well with the X-ray crystallography results; however, the mechanism of the necessary charge compensation could not be identified. The cation arrangements in the crystal structures of thorium and uranium polymetaphosphates have been studied in terms of Voronoi-Dirichlet polyhedra. Different conformations of the tetraphosphate polyanions were observed in the crystal structures of Th(P{sub 4}O{sub 12}) and U(P{sub 4}O{sub 12}). The Raman spectrum of a single crystal of Th(P{sub 4}O{sub 12}) was recorded, and the bands were assigned. (Copyright copyright 2015 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  7. Thorium effect on the oxidation of uranium: Photoelectron spectroscopy (XPS/UPS) and cyclic voltammetry (CV) investigation on (U{sub 1−x}Th{sub x})O{sub 2} (x = 0 to 1) thin films

    Energy Technology Data Exchange (ETDEWEB)

    Cakir, P., E-mail: pelincakir@outlook.com [European Commission, Joint Research Centre, P.O. Box 2340, D-76125, Karlsruhe (Germany); Department of Radiation Science and Technology, Delft University of Technology, Mekelweg 15, 2629, JB Delft (Netherlands); Eloirdi, R.; Huber, F. [European Commission, Joint Research Centre, P.O. Box 2340, D-76125, Karlsruhe (Germany); Konings, R.J.M. [European Commission, Joint Research Centre, P.O. Box 2340, D-76125, Karlsruhe (Germany); Department of Radiation Science and Technology, Delft University of Technology, Mekelweg 15, 2629, JB Delft (Netherlands); Gouder, T. [European Commission, Joint Research Centre, P.O. Box 2340, D-76125, Karlsruhe (Germany)

    2017-01-30

    Highlights: • XRD and XPS data of U{sub x}Th{sub 1-x}O{sub 2} films are in agreement with data obtained on bulk. • Oxygen affinity of thorium is much stronger than uranium. • Oxidation of uranium decreases as a function of thorium in the matrix. • XPS made pre and post CV shows thorium enrichment indicating a protective layer. • Higher initial uranium content is directly proportional to higher oxidation states. - Abstract: Thin films of U{sub 1−x}Th{sub x}O{sub 2} (x = 0 to 1) have been deposited via reactive DC sputter technique and characterized by X-ray/Ultra-violet Photoelectron Spectroscopy (XPS/UPS), X-ray Powder Diffractometer (XRD) and Cyclic Voltammetry (CV) in order to understand the effect of Thorium on the oxidation mechanism. During the deposition, the competition between uranium and thorium for oxidation showed that thorium has a much higher affinity for oxygen. Deposition conditions, time and temperature were also the subject of this study, to look at the homogeneity and the stability of the films. While core level and valence band spectra were not altered by the time of deposition, temperature was affecting the oxidation state of uranium and the valence band due to the mobility increase of oxygen through the film. X-ray diffraction patterns, core level spectra obtained for U{sub 1−x}Th{sub x}O{sub 2} versus the composition showed that lattice parameters follow the Vegard's law and together with the binding energies of U-4f and Th-4f are in good agreement with literature data obtained on bulk compounds. To study the effect of thorium on the oxidation of U{sub 1−x}Th{sub x}O{sub 2} films, we used CV experiments at neutral pH of a NaCl solution in contact with air. The results indicated that thorium has an effect on the uranium oxidation as demonstrated by the decrease of the current of the oxidation peak of uranium. XPS measurements made before and after the CV, showed a relative enrichment of thorium at the extent of uranium at

  8. On-line solid phase extraction using ion-pair microparticles combined with ICP-OES for the simultaneous preconcentration and determination of uranium and thorium

    Energy Technology Data Exchange (ETDEWEB)

    Yousefi, Seyed Reza; Zolfonoun, Ehsan [Nuclear Science and Technology Research Institute, Tehran (Iran, Islamic Republic of). NFCRS

    2016-07-01

    In this work, after on-line and in-situ solid phase extraction technique was used for the extraction and preconcentration of uranium and thorium from aqueous samples prior to inductively coupled plasma optical emission spectrometry (ICP-OES) determination. In this method, sodium hexafluorophosphate (as an ion-pairing agent) was added to the sample solution containing the cationic surfactant (dodecyltrimethylammonium bromide) and the complexing agent (dibenzoylmethane). A cloudy solution was formed as a result of formation of an ion pair between surfactant and hexafluorophosphate. The solid microparticles were passed through a microcolumn filter and the adsorbed microparticles were subsequently eluted with acid, which was directly introduced into the ICP-OES nebulizer. The main variables affecting the pre-concentration and determination steps of uranium and thorium were studied and optimized. Under the optimum conditions, the enhancement factors of 97 and 95 and the detection limits of 0.52 and 0.21 μg L{sup -1} were obtained for uranium and thorium, respectively.

  9. The crystal chemistry of novel thorium and uranium compounds with oxo-anions from group VI of periodic table (S, Se, Te, Cr, Mo and W)

    Energy Technology Data Exchange (ETDEWEB)

    Xiao, Bin

    2016-01-26

    This dissertation focus on the synthesis, phase studies and physicochemical properties of novel thorium and uranium compounds with the Group VI (S, Se, Te, Cr, Mo, W) of the Periodic Table. All the studied compounds are listed in Table 2.2 from the page 15. I subdivided all the newly synthesized compounds into several chapters according to their structural and topological differences. First, for thorium molybdates and tungstates, almost all of these compounds are based on corner-sharing of ThO{sub x} (x = 6, 8 and 9) and MoO{sub 4} or WO{sub x} (x = 4, 5, 6) polyhedra. Interestingly, all these compounds can be seen as derived from a pure thorium molybdate compound (ThMo{sub 2}O{sub 8}) which was isolated from high-temperature solid-state synthesis method. Therefore, the polymorphs of this most basic ThMo{sub 2}O{sub 8} compound is firstly introduced (see Chapter 3.1 from page 18). The thermodynamic, electronic and vibrational properties of all investigated ThMo{sub 2}O{sub 8} polymorphs were studied using ab initio calculations. Then, two subfamilies of thorium molybdates, that is, rubidium thorium molybdate and cesium thorium molybdate and their thermal and vibrational behaviors were discussed in details in Chapter 4.1 from page 37 and Chapter 4.2 from page 50, respectively. Moreover, some new insights about the complexity of thorium tungstates were also discussed (Chapter 4.3 from page 59). Some novel thorium molybdate and chromate compounds synthesized from aqueous condition are discussed in Chapter 5 from page 71. In the Chapter 8.2.4, the stereochemistry for thorium and uranium compounds are introduced, especially thorium selinites and uranyl tellurites (see Chapter 6.1 from page 82), thorium tellurites (Chapter 6.2 from page 93), and uranyl tellurites (Chapter 6.3 from page 99 for sodium uranyl tellurium and Chapter 6.4 from page 110 for potassium uranyl tellurium, respectively). In the actinide tellurium systems, additional MoO{sub 3}/WO{sub 3} were also

  10. Sustainability of thorium-uranium in pebble-bed fluoride salt-cooled high temperature reactor

    Directory of Open Access Journals (Sweden)

    Zhu Guifeng

    2016-01-01

    Full Text Available Sustainability of thorium fuel in a Pebble-Bed Fluoride salt-cooled High temperature Reactor (PB-FHR is investigated to find the feasible region of high discharge burnup and negative Flibe (2LiF-BeF2 salt Temperature Reactivity Coefficient (TRC. Dispersion fuel or pellet fuel with SiC cladding and SiC matrix is used to replace the tristructural-isotropic (TRISO coated particle system for increasing fuel loading and decreasing excessive moderation. To analyze the neutronic characteristics, an equilibrium calculation method of thorium fuel self-sustainability is developed. We have compared two refueling schemes (mixing flow pattern and directional flow pattern and two kinds of reflector materials (SiC and graphite. This method found that the feasible region of breeding and negative Flibe TRC is between 20 vol% and 62 vol% fuel loading in the fuel. A discharge burnup could be achieved up to about 200 MWd/kgHM. The case with directional flow pattern and SiC reflector showed superior burnup characteristics but the worst radial power peak factor, while the case with mixing flow pattern and SiC reflector, which was the best tradeoff between discharge burnup and radial power peak factor, could provide burnup of 140 MWd/kgHM and about 1.4 radial power peak factor with 50 vol% dispersion fuel. In addition, Flibe salt displays good neutron properties as a coolant of quasi-fast reactors due to the strong 9Be(n,2n reaction and low neutron absorption of 6Li (even at 1000 ppm in fast spectrum. Preliminary thermal hydraulic calculation shows good safety margin. The greatest challenge of this reactor may be the decades irradiation time of the pebble fuel.

  11. Dioxins, furans, biphenyls, arsenic, thorium and uranium in natural and anthropogenic sources of phosphorus and calcium used in agriculture

    Energy Technology Data Exchange (ETDEWEB)

    Avelar, A.C., E-mail: avelara@ufmg.br [Department of Animal Sciences, Veterinary School, Universidad de Federal de Minas Gerais Avenida Antonio Carlos, 6627 Campus UFMG, Belo Horizonte (Brazil); Ferreira, W.M. [Department of Animal Sciences, Veterinary School, Universidad de Federal de Minas Gerais Avenida Antonio Carlos, 6627 Campus UFMG, Belo Horizonte (Brazil); Pemberthy, D. [Spanish Council for Scientific Research (CSIC), Institute of Environmental Assessment and Water Research, C/ Jordi Girona 18-26, 08034 Barcelona (Spain); Universidad de Antioquia, Departamento de Ingeniería Química, Facultad de Ingeniería, Grupo Catálisis Ambiental, Calle 70 No. 52-2, Medellín (Colombia); Abad, E. [Spanish Council for Scientific Research (CSIC), Institute of Environmental Assessment and Water Research, C/ Jordi Girona 18-26, 08034 Barcelona (Spain); Amaral, M.A. [Department of Animal Sciences, Veterinary School, Universidad de Federal de Minas Gerais Avenida Antonio Carlos, 6627 Campus UFMG, Belo Horizonte (Brazil)

    2016-05-01

    The aim of this study was to assess the presence of dioxins, furans and biphenyls, and the inorganic contaminants such as arsenic (As), thorium (Th) and uranium (U) in three main products used in Agriculture in Brazil: feed grade dicalcium phosphate, calcined bovine bone meal and calcitic limestone. The first two are anthropogenic sources of phosphorus and calcium, while calcitic limestone is a natural unprocessed mineral. Regarding to dioxin-like substances, all samples analyzed exhibited dioxins (PCDD) and furans (PCDF) and dioxin-like polychlorinated biphenyls (dl-PCBs) concentrations below limit of detection (LOD). In general, achieved is in accordance with regulation in Brazil where is established a maximum limit in limestone used in the citric pulp production (0.50 pg WHO-TEQ g{sup −1}). In addition, reported data revealed very low levels for limestone in comparison with similar materials reported by European legislation. As result for toxic metals, achieved data were obtained using Instrumental Neutron Activation Analysis (INAA). On one hand, limestone sample exhibits the largest arsenic concentration. On another hand, dicalcium phosphate exhibited the largest uranium concentration, which represents a standard in animal nutrition. Therefore, it is phosphorus source in the animal feed industry can be a goal of concern in the feed field. - Highlights: • PCDD/Fs dl- PCBs is not a matter since levels below the LOD in phosphate materials subject of study. • Significant accumulation of As and U in Limestone. Th was originally found in dicalcium phosphate. • High concentration of U in dicalcium phosphate suggests that a special attention should be paid.

  12. Analysis of radon, uranium 238 and thorium 232 in potable waters: Dose to adult members of the Moroccan urban population

    Energy Technology Data Exchange (ETDEWEB)

    Misdaq, M.A. [Nuclear Physics and Techniques Laboratory, Faculty of Sciences Semlalia, BP 2390, University Cadi Ayyad, Marrakech (Morocco)], E-mail: misdaq@ucam.ac.ma; Ouabi, H. [Nuclear Physics and Techniques Laboratory, Faculty of Sciences Semlalia, BP 2390, University Cadi Ayyad, Marrakech (Morocco); Merzouki, A. [Nuclear Physics and Techniques Laboratory, Faculty of Sciences Semlalia, BP 2390, University Cadi Ayyad, Marrakech (Morocco); Remote Sensing and Geomatics of the Environmental Laboratory, Ottawa-Carleton Geoscience Centre, Marion Hall, 140 Louis Pasteur, Ottawa, ON, KIN6N5 (Canada)

    2007-10-15

    Uranium ({sup 238}U) and thorium ({sup 232}Th) concentrations as well as radon ({sup 222}Rn) and thoron ({sup 220}Rn) alpha-activities per unit volume have been measured inside various potable water samples collected from nineteen cities in Morocco by using CR-39 and LR-115 type II solid state nuclear track detectors (SSNTDs). Measured radon alpha-activities ranged from (0.37 {+-} 0.02) Bq l{sup -1} to (13.6 {+-} 1.10) Bq l{sup -1} for the potable water samples studied. Alpha-activities due to radon from the ingestion of the studied potable water samples were determined in different compartments of the gastrointestinal system by using the ICRP compartmental model for radon. Annual committed equivalent doses due to radon were evaluated in the gastrointestinal compartments from the ingestion of the potable water samples studied. The influence of the target tissue mass, radon intake and alpha-activity integral due to radon on the annual committed equivalent doses in the gastrointestinal compartments was investigated.

  13. Uranium and thorium enrichment in rocks from the base of DSDP hole 465A, Hess Rise, central North Pacific

    Energy Technology Data Exchange (ETDEWEB)

    Hein, J.R.; Koski, R.A.; Morgenson, L.A. (Geological Survey, Menlo Park, CA (USA))

    1982-07-01

    Uranium and thorium are concentrated in Cretaceous limestone, chert, ash, basalt, and other rock types at Deep Sea Drilling Project Site 465 located on the southern Hess Rise in the central North Pacific. U concentrations, up to 194 ppm on a carbonate-free basis, are among the highest recorded for any deep-sea deposits. U was initially derived from seawater and concentrated by absorption on terrigenous (humic) organic matter in limestone in a shallow marine environment. U and Th were probably concentrated further by low-temperature hydrothermal fluids emanating from the basaltic basement. Mainly montmorillonite, an alteration product of basalt and ash, and organic matter in sedimentary rocks acted as hosts for U and Th. The unique combination of sediments rich in humic organic matter, abundant smectite in altered ash and basalt, and warm hydrothermal solutions provided the necessary conditions for migration and concentration of U and Th. To better understand the conditions limiting the migrating and concentration of U and Th, other rocks deposited during the ocean-wide Cretaceous anoxic events should be analyzed for these elements.

  14. Assessment of radionuclides (uranium and thorium) atmospheric pollution around Manjung district, Perak using moss as bio-indicator

    Energy Technology Data Exchange (ETDEWEB)

    Arshad, Nursyairah, E-mail: nursyairah1990@gmail.com; Hamzah, Zaini; Wood, Ab. Khalik [Faculty of Applied Sciences, Universiti Teknologi MARA, 40450, Shah Alam Selangor (Malaysia); Saat, Ahmad [Faculty of Applied Sciences, Universiti Teknologi MARA, 40450, Shah Alam Selangor (Malaysia); Institute of Science, Universiti Teknologi MARA, 40450, Shah Alam Selangor (Malaysia)

    2016-01-22

    Bio-monitoring method using mosses have been widely done around the world and the effectiveness has been approved. Mosses can be used to assess the levels of atmospheric pollution as mosses pick up nutrients from the atmosphere and deposition retaining many trace elements. In this study, the deposition of two radionuclides; uranium (U) and thorium (Th) around Manjung districts have been evaluated using Leucobryum aduncum as bio-monitoring medium. The samples were collected from 24 sampling sites covering up to 40 km radius to the North, North-East and South-East directions from Teluk Rubiah. The concentrations of U and Th in moss samples were analysed using Energy Dispersive X-Ray Fluorescence (EDXRF) Spectrometer. The concentrations of Th are in the range of 0.07-2.09 mg/kg. Meanwhile, the concentrations of U in the moss are in the range of 0.03-0.18 mg/kg. The Enrichment Factor (EF) was calculated to determine the origin of the radionuclides distributions. Other than that, the distribution maps were developed to observe the distribution of the radionuclides around the study area.

  15. Determination of the coefficient of uranium and thorium distribution in phosphogypsum for their use in sanitary landfills

    Energy Technology Data Exchange (ETDEWEB)

    Marchesi, Marcos Vinicius A.; Hama, Naruhiko; Jacomino, Vanusa M. F.; Ladeira, Ana Claudia Q.; Cota, Stela D. S., E-mail: mvmarchesi@hotmail.com, E-mail: sdsc@cdtn.br, E-mail: vmfj@cdtn.br, E-mail: ana.ladeira@cdtn.br, E-mail: naruhikohama@hotmail.com [Centro de Desenvolvimento da Tecnologia Nuclear (CDTN/CNEN-MG), Belo Horizonte, MG (Brazil); Nascimento, Marcos Roberto Lopes do; Taddei, Maria Helena, E-mail: pmarcos@cnen.gov.br, E-mail: mhtaddei@cnen.gov.br [Comissao Nacional de Energia Nuclear (LAPOC/CNEN), Pocos de Caldas, MG (Brazil). Laboratorio de Pocos de Caldas

    2013-07-01

    Phosphogypsum is a byproduct from the production of phosphoric acid, and contain radionuclides, heavy metals and metalloids from phosphate rock. It represents a risk to the environment if improperly stored. Because it is composed mainly of dihydrated calcium sulphate, phosphogypsum can be used in anaerobic environments such as those found in landfills to accelerate microbial processes of decomposition of municipal solid waste and thus increase the life of these facilities. One of the options of your application being studied is the use of phosphogypsum replacing the covers of soil/clay in landfills. Besides reducing the demand for soil and clay, this application would be an alternative to disposal of the waste, since the alternatives are not sufficient for more than five million tons produced per year in Brazil. To ensure the safety of this application, the potential environmental impact of contaminants in phosphogypsum should be evaluated. The rate of leaching of contaminants are being studied by determining the coefficient of distribution of the contaminants in the phosphogypsum. Batch tests were performed by mixing different proportions of slurry and phosphogypsum. This work presents the results for the chain of uranium and natural thorium.

  16. MACHINING TECHNIQUES AND PROCEDURES FOR URANIUM, GRAPHITE, TITANIUM, ZIRCONIUM, THORIUM, TANTALUM, BERYLLIUM, BISMUTH, LITHIUM, AND STELLITE

    Energy Technology Data Exchange (ETDEWEB)

    Davis, C.

    1952-11-04

    Techniqnes are presented which are applicable in machining materinls such as U, graphite, Ti, Zr, Th, Ta, Be, Bi, Li, and stellite. Included in the general considerations are factors related to machinability of the materials, operating condition of the machines, and the condition of the cutting tools. In addition, industrial hygtene and safety aspects are examined. The techniques for each material are discussed in detail, the greatest attention being focused on uranium.

  17. Induced Formation of Chelating Agents by Pseudomonas aeruginosa Grown in Presence of Thorium and Uranium

    Science.gov (United States)

    1985-07-01

    increased. At concentrations of 1000 ppm and higher, there was an extended lag period followed by reduction in growth. Uranium has a stronger...formation !s rapid (Wl min) at room temperature , with a lower sensitivity limit of 0.05 ppm for Th and U under experimental conditions used. Since the...Nellands J1 (1977) Siderophores: Biochemical ecology and mechanism of iron transport in enterobacteria . In: Raymond KN (ed) Hlinorganic Chemistry-1I

  18. Photochemical route to actinide-transition metal bonds: synthesis, characterization and reactivity of a series of thorium and uranium heterobimetallic complexes

    Energy Technology Data Exchange (ETDEWEB)

    Ward, Ashleigh; Lukens, Wayne; Lu, Connie; Arnold, John

    2014-04-01

    A series of actinide-transition metal heterobimetallics has been prepared, featuring thorium, uranium and cobalt. Complexes incorporating the binucleating ligand N[-(NHCH2PiPr2)C6H4]3 and Th(IV) (4) or U(IV) (5) with a carbonyl bridged [Co(CO)4]- unit were synthesized from the corresponding actinide chlorides (Th: 2; U: 3) and Na[Co(CO)4]. Irradiation of the isocarbonyls with ultraviolet light resulted in the formation of new species containing actinide-metal bonds in good yields (Th: 6; U: 7); this photolysis method provides a new approach to a relatively rare class of complexes. Characterization by single-crystal X-ray diffraction revealed that elimination of the bridging carbonyl is accompanied by coordination of a phosphine arm from the N4P3 ligand to the cobalt center. Additionally, actinide-cobalt bonds of 3.0771(5) and 3.0319(7) for the thorium and uranium complexes, respectively, were observed. The solution state behavior of the thorium complexes was evaluated using 1H, 1H-1H COSY, 31P and variable-temperature NMR spectroscopy. IR, UV-Vis/NIR, and variable-temperature magnetic susceptibility measurements are also reported.

  19. Standard test method for analysis of total and isotopic uranium and total thorium in soils by inductively coupled plasma-mass spectrometry

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2008-01-01

    1.1 This test method covers the measurement of total uranium (U) and thorium (Th) concentrations in soils, as well as the determination of the isotopic weight percentages of 234U, 235U, 236U, and 238U, thereby allowing for the calculation of individual isotopic uranium activity or total uranium activity. This inductively coupled plasma-mass spectroscopy (ICP-MS) method is intended as an alternative analysis to methods such as alpha spectroscopy or thermal ionization mass spectroscopy (TIMS). Also, while this test method covers only those isotopes listed above, the instrumental technique may be expanded to cover other long-lived radioisotopes since the preparation technique includes the preconcentration of the actinide series of elements. The resultant sample volume can be further reduced for introduction into the ICP-MS via an electrothermal vaporization (ETV) unit or other sample introduction device, even though the standard peristaltic pump introduction is applied for this test method. The sample preparatio...

  20. Determination of specific alpha-emitting radionuclides (uranium, plutonium, thorium and polonium) in water using [Ba+Fe]-coprecipitation method.

    Science.gov (United States)

    Suarez-Navarro, J A; Pujol, Ll; Suarez-Navarro, M J

    2017-12-01

    The indicative dose (ID) is one of the parameters established in the current European directive for water intended for human consumption. To determine the ID, it is necessary to know the activity concentration of: 238U, 234U, 226Ra, 210Po, 239,240Pu and 241Am. The existing methods to determine these radionuclides involve complex radiochemical separations (ionic exchange columns, extraction chromatography, etc.), followed by measurements with a semiconductor detector, laboratory procedures that are time-consuming and costly. As a lower cost alternative that reduces measuring and preparation times, avoids the need for a self-absorption correction and the use of tracers, and above all that can be used in any laboratory, methods based on liquid-liquid extraction and selective co-precipitation were developed. These methodologies offer high separation recovery and selectivity, and the measurements are made using a gas proportional counter or a solid ZnS(Ag) scintillation counter. The separation factor ranged between 91.4% and 100.0% for all alpha-emitting radionuclides across the different methods. The activity concentration for each method was computed through linear equations that represent the relationship between the activity and selectivity of the different alpha-emitting radionuclides. This mathematical procedure simplifies the radiochemical separations and provides more accurate activity concentrations. The results of the internal and external validation studies proved that the proposed method is suitable for determining 241Am, 226Ra, uranium, plutonium, thorium and 210Po in water samples. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. Determination of trace element concentrations and stable lead, uranium and thorium isotope ratios by quadrupole-ICP-MS in NORM and NORM-polluted sample leachates

    Energy Technology Data Exchange (ETDEWEB)

    Mas, J.L., E-mail: ppmasb@us.es [Dpto. Fisica Aplicada I, EPS, Universidad de Sevilla, 41012 Sevilla (Spain); Villa, M. [Servicio de Radioisotopos, Centro de Investigacion, Tecnologia e Innovacion (CITIUS), Universidad de Sevilla, Avda. Reina Mercedes 4b, 41012 Sevilla (Spain); Dpto. Fisica Aplicada II, ETS de Arquitectura, Universidad de Sevilla, Avda. Reina Mercedes 2, 41012 Sevilla (Spain); Hurtado, S. [Servicio de Radioisotopos, Centro de Investigacion, Tecnologia e Innovacion (CITIUS), Universidad de Sevilla, Avda. Reina Mercedes 4b, 41012 Sevilla (Spain); Garcia-Tenorio, R. [Dpto. Fisica Aplicada II, ETS de Arquitectura, Universidad de Sevilla, Avda. Reina Mercedes 2, 41012 Sevilla (Spain)

    2012-02-29

    Highlights: Black-Right-Pointing-Pointer Polluted sediment and NORM samples. Black-Right-Pointing-Pointer An efficient yet fast process allowing multi-parametric determinations in <3 days. Black-Right-Pointing-Pointer Trace element concentrations, Pb, Th and U isotope ratios with a single instrument. - Abstract: This work focuses on the monitoring of the potential pollution in scenarios that involve NORM-related industrial activities (environmental or in-door scenarios). The objective was to develop a method to determine extent and origin of the contamination, suitable for monitoring (i.e. simple, fast and economical) and avoiding the use of too many different instruments. It is presented a radiochemical method that allows the determination of trace element concentrations and {sup 206}Pb/{sup 207}Pb/{sup 208}Pb, {sup 238}U/{sup 234}U and {sup 232}Th/{sup 230}Th isotope ratios using a single sample aliquot and a single instrument (ICP-QMS). Eichrom UTEVA{sup Registered-Sign} extraction chromatography minicolumns were used to separate uranium and thorium in sample leachates. Independent ICP-MS determinations of uranium and thorium isotope ratios were carried out afterwards. Previously a small aliquot of the leachate was used for the determination of trace element concentrations and lead isotope ratios. Several radiochemical arrangements were tested to get maximum performances and simplicity of the method. The performances of the method were studied in terms of chemical yields of uranium and thorium and removal of the potentially interfering elements. The established method was applied to samples from a chemical industry and sediments collected in a NORM-polluted scenario. The results obtained from our method allowed us to infer not only the extent, but also the sources of the contamination in the area.

  2. Adapting the deep burn in-core fuel management strategy for the gas turbine - modular helium reactor to a uranium-thorium fuel

    Energy Technology Data Exchange (ETDEWEB)

    Talamo, Alberto [Department of Nuclear and Reactor Physics, Royal Institute of Technology, Roslagstullsbacken 21, S-10691, Stockholm (Sweden)]. E-mail: alby@neutron.kth.se; Gudowski, Waclaw [Department of Nuclear and Reactor Physics, Royal Institute of Technology, Roslagstullsbacken 21, S-10691, Stockholm (Sweden)

    2005-11-15

    In 1966, Philadelphia Electric has put into operation the Peach Bottom I nuclear reactor, it was the first high temperature gas reactor (HTGR); the pioneering of the helium-cooled and graphite-moderated power reactors continued with the Fort St. Vrain and THTR reactors, which operated until 1989. The experience on HTGRs lead General Atomics to design the gas turbine - modular helium reactor (GT-MHR), which adapts the previous HTGRs to the generation IV of nuclear reactors. One of the major benefits of the GT-MHR is the ability to work on the most different types of fuels: light water reactors waste, military plutonium, MOX and thorium. In this work, we focused on the last type of fuel and we propose a mixture of 40% thorium and 60% uranium. In a uranium-thorium fuel, three fissile isotopes mainly sustain the criticality of the reactor: {sup 235}U, which represents the 20% of the fresh uranium, {sup 233}U, which is produced by the transmutation of fertile {sup 232}Th, and {sup 239}Pu, which is produced by the transmutation of fertile {sup 238}U. In order to compensate the depletion of {sup 235}U with the breeding of {sup 233}U and {sup 239}Pu, the quantity of fertile nuclides must be much larger than that one of {sup 235}U because of the small capture cross-section of the fertile nuclides, in the thermal neutron energy range, compared to that one of {sup 235}U. At the same time, the amount of {sup 235}U must be large enough to set the criticality condition of the reactor. The simultaneous satisfaction of the two above constrains induces the necessity to load the reactor with a huge mass of fuel; that is accomplished by equipping the fuel pins with the JAERI TRISO particles. We start the operation of the reactor with loading fresh fuel into all the three rings of the GT-MHR and after 810 days we initiate a refueling and shuffling schedule that, in 9 irradiation periods, approaches the equilibrium of the fuel composition. The analysis of the k {sub eff} and mass

  3. On the sequential separation and quantification of (237)Np, (241)Am, thorium, plutonium, and uranium isotopes in environmental and urine samples.

    Science.gov (United States)

    Vasile, M; Jacobs, K; Bruggeman, M; Van Hoecke, K; Dobney, A; Verrezen, F

    2017-07-13

    The implementation of the one-pass-through separation technique using two stacked chromatography columns of TEVA - TRU resins for the separation of (237)Np, (241)Am, thorium, plutonium and uranium from environmental and urine samples was investigated. The sequential separation technique proved to be successful and gave similar results to those obtained when using individual separations. The analysis time was considerably improved. The amount of chemical waste was also reduced by 50% and the use of HClO4 was avoided. The technique of ICP-MS was also investigated as a complementary technique to alpha-spectrometry. Copyright © 2017 Elsevier Ltd. All rights reserved.

  4. Model for the behaviour of thorium and uranium fuels at pelletization; Modelo para o comportamento de microesferas combustiveis de torio e uranio na peletizacao

    Energy Technology Data Exchange (ETDEWEB)

    Ferreira Neto, Ricardo Alberto

    2000-11-15

    In this work, a model for the behaviour of thorium-uranium-mixed oxide microspheres in the pelletizing process is presented. This model was developed in a program whose objective was to demonstrate the viability of producing fissile material through the utilization of thorium in pressurized water reactors. This is important because it allows the saving of the strategic uranium reserves, and makes it possible the nuclear utilization of the large brazilian thorium reserves. The objective was to develop a model for optimizing physical properties of the microspheres, such as density, fracture strength and specific surface, so as to produce fuel pellets with microstructure, density, open porosity and impurity content, in accordance with the fuel specification. And, therefore, to adjust the sol-gel processing parameters in order to obtain these properties, and produce pellets with an optimized microstructure, adequate to a stable behaviour under irradiation. The model made it clear that to achieve this objective, it is necessary to produce microspheres with density and specific surface as small as possible. By changing the sol-gel processing parameters, microspheres with the desired properties were produced, and the model was experimentally verified by manufacturing fuel pellets with optimized microstructures, density, open porosity and impurity content, meeting the specifications for this new nuclear fuel for pressurized water reactors. Furthermore it was possible to obtain mathematical expressions that enables to calculate from the microspheres properties and the utilized compaction pressure, the sinter density that will be obtained in the sintered pellet and the necessary compaction pressure to reach the sintered density specified for the fuel. (author)

  5. Depth-Resolved Cathodoluminescence of Thorium Dioxide

    Science.gov (United States)

    2013-03-01

    1 238Pu……………... Plutonium -238... plutonium -239 (239Pu)-based nuclear weapons. Thorium also results in less highly radioactive waste in comparison to the uranium fuels. Thorium is four...spectra. Direct determination of fractional parts per million amounts of rare earths in thorium.” Analytical Chemistry , 42, no. 3 (1970): 325-329. B

  6. Uranium, radium and thorium in soils with high-resolution gamma spectroscopy, MCNP-generated efficiencies, and VRF non-linear full-spectrum nuclide shape fitting

    Science.gov (United States)

    Metzger, Robert; Riper, Kenneth Van; Lasche, George

    2017-09-01

    A new method for analysis of uranium and radium in soils by gamma spectroscopy has been developed using VRF ("Visual RobFit") which, unlike traditional peak-search techniques, fits full-spectrum nuclide shapes with non-linear least-squares minimization of the chi-squared statistic. Gamma efficiency curves were developed for a 500 mL Marinelli beaker geometry as a function of soil density using MCNP. Collected spectra were then analyzed using the MCNP-generated efficiency curves and VRF to deconvolute the 90 keV peak complex of uranium and obtain 238U and 235U activities. 226Ra activity was determined either from the radon daughters if the equilibrium status is known, or directly from the deconvoluted 186 keV line. 228Ra values were determined from the 228Ac daughter activity. The method was validated by analysis of radium, thorium and uranium soil standards and by inter-comparison with other methods for radium in soils. The method allows for a rapid determination of whether a sample has been impacted by a man-made activity by comparison of the uranium and radium concentrations to those that would be expected from a natural equilibrium state.

  7. Uranium, radium and thorium in soils with high-resolution gamma spectroscopy, MCNP-generated efficiencies, and VRF non-linear full-spectrum nuclide shape fitting

    Directory of Open Access Journals (Sweden)

    Metzger Robert

    2017-01-01

    Full Text Available A new method for analysis of uranium and radium in soils by gamma spectroscopy has been developed using VRF (“Visual RobFit” which, unlike traditional peak-search techniques, fits full-spectrum nuclide shapes with non-linear least-squares minimization of the chi-squared statistic. Gamma efficiency curves were developed for a 500 mL Marinelli beaker geometry as a function of soil density using MCNP. Collected spectra were then analyzed using the MCNP-generated efficiency curves and VRF to deconvolute the 90 keV peak complex of uranium and obtain 238U and 235U activities. 226Ra activity was determined either from the radon daughters if the equilibrium status is known, or directly from the deconvoluted 186 keV line. 228Ra values were determined from the 228Ac daughter activity. The method was validated by analysis of radium, thorium and uranium soil standards and by inter-comparison with other methods for radium in soils. The method allows for a rapid determination of whether a sample has been impacted by a man-made activity by comparison of the uranium and radium concentrations to those that would be expected from a natural equilibrium state.

  8. Thorium and the Third Fuel

    Energy Technology Data Exchange (ETDEWEB)

    Dukert, Joseph M.

    1970-01-01

    This booklet discusses energy sources for nuclear power plants. Uranium-235 by itself will not be able to handle the energy needs. The two man-made supplements that can be used for nuclear power plants energy sources are plutonium and uranium-233. Uranium-233 is an isotope that appears as a result of radioactive decay after neutrons have been absorbed in thorium-232. This uranium-233 is called the third fuel.

  9. Formation of uranium-thorium-rich bitumen nodules in the Lockne impact structure, Sweden: A mechanism for carbon concentration at impact sites

    Science.gov (United States)

    Lindgren, Paula; Parnell, John; Norman, Craig; Mark, Darren F.; Baron, Martin; Ormö, Jens; Sturkell, Erik; Conliffe, James; Fraser, Wesley

    The Ordovician Lockne impact structure is located in central Sweden. The target lithology consisted of limestone and black unconsolidated shale overlaying a Precambrian crystalline basement. The Precambrian basement is uranium-rich, and the black shale is both uranium- and organic-rich. This circumstance makes Lockne a good candidate for testing the occurrence of U-Th-rich bitumen nodules in an impact structure setting. U-Th-rich bitumen nodules are formed through irradiation; hence the increase in the complexity of organic matter by a radioactive (uranium- and thorium-rich) mineral phase. U-Th-rich bitumen nodules were detected in crystalline impact breccia and resurge deposits from the impact structure, but samples of non-impact-affected rocks from outside the impact structure do not contain any U-Th-rich bitumen nodules. This implies that in the Lockne impact structure, the nodules are associated with impact-related processes. U-Th-rich bitumen nodules occur throughout the geological record and are not restricted to an impact structure setting, but our studies at Lockne show that this process of irradiation can readily occur in impact structures where fracturing of rocks and a post-impact hydrothermal system enhances fluid circulation. The irradiation of organic matter by radioactive minerals has previously been proposed as a process for concentration of carbon on the early Earth. Impact structures are suggested as sites for prebiotic chemistry and primitive evolution, and irradiation by radioactive minerals could be an important mechanism for carbon concentration at impact sites.

  10. New insights into thorium and uranium oxo-arsenic (III/V) and oxo-phosphates (V) crystal chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Yu, Na

    2015-12-11

    -phosphate(V) phases that were derived from the before mentioned methods. They can be separated into several main parts according to the structural features: layers in U(VI) phases (chapter 3); cations driving structural diversity of thorium arsenates and phosphates (chapter 4 and 5); uranium metaphosphate with (PO{sub 3}){sub n}{sup n-} polymeric chains (chapter 6); mixed-valent arsenic(III/V) Th compounds obtained under extreme pressure (chapter 7); series of compounds adopting the typical structure type of KTh{sub 2}(AsO{sub 4}){sub 3} and presented by ATh{sub 2}(AsO{sub 4}){sub 3}(A= K, Rb, Cs, Ag), LiTh{sub 2}(PO{sub 4}){sub 3} and BU{sup IV}{sub 2}(PO{sub 4}){sub 3} (B= Rb, Cs); tri-phosphate and tri-arsenate T{sub 3}O{sub 10} units in the ATh(T{sub 3}O{sub 10}) (A= Rb, Cs; T= P, As) family (chapter 7).

  11. Synthesis, sintering and dissolution of thorium and uranium (IV) mixed oxide solid solutions: influence of the method of precursor preparation; Synthese, frittage et caracterisation de solutions solides d'oxydes mixtes de thorium et d'uranium (IV): influence de la methode de preparation du precurseur

    Energy Technology Data Exchange (ETDEWEB)

    Hingant, N

    2008-12-15

    Mixed actinide dioxides are currently considered as potential fuels for the third and fourth generations of nuclear reactors. In this context, thorium-uranium (IV) dioxide solid solutions were studied as model compounds to underline the influence of the method of preparation on their physico-chemical properties. Two methods of synthesis, both based on the initial precipitation of oxalate precursors have been developed. The first consisted in the direct precipitation ('open' system) while the second involved hydrothermal conditions ('closed' system). The second method led to a significant improvement in the crystallization of the samples especially in the field of the increase of the grain size. In these conditions, the formation of a complete solid solution Th{sub 1-x}U{sub x}(C{sub 2}O{sub 4}){sub 2}.2H{sub 2}O was prepared between both end-members. Its crystal structure was also resolved. Whatever the initial method considered, these compounds led to the final dioxides after heating above 400 C. The various steps associated to this transformation, involving the dehydration of precursors then the decomposition of oxalate groups have been clarified. Moreover, the use of wet chemistry methods allowed to reduce the sintering temperature of the final thorium-uranium (IV) dioxide solid solutions. Whatever the method of preparation considered, dense samples (95% to 97% of the calculated value) were obtained after only 3 hours of heating at 1500 C. Additionally, the use of hydrothermal conditions significantly increased the grain size, leading to the reduction of the occurrence of the grain boundaries and of the global residual porosity. The significant improvement in the homogeneity of cations distribution in the samples was also highlighted. Finally, the chemical durability of thorium-uranium (IV) dioxide solid solutions was evaluated through the development of leaching tests in nitric acid. The optimized homogeneity especially in terms of the

  12. Design of a boiling water reactor core based on an integrated blanket-seed thorium-uranium concept

    Energy Technology Data Exchange (ETDEWEB)

    Nunez-Carrera, Alejandro [Facultad de Ingenieria, Universidad Nacional Autonoma de Mexico, Laboratorio de Analisis en Ingenieria de Reactores Nucleares, Paseo Cuauhnahuac 8532, 62550 Jiutepec, Mor. (Mexico); Comision Nacional de Seguridad Nuclear y Salvaguardias, Dr. Barragan 779, Col. Narvarte, 03020 Mexico, D.F. (Mexico); Francois, Juan Luis [Facultad de Ingenieria, Universidad Nacional Autonoma de Mexico, Laboratorio de Analisis en Ingenieria de Reactores Nucleares, Paseo Cuauhnahuac 8532, 62550 Jiutepec, Mor. (Mexico)]. E-mail: jlfl@fi-b.unam.mx; Martin-del-Campo, Cecilia [Facultad de Ingenieria, Universidad Nacional Autonoma de Mexico, Laboratorio de Analisis en Ingenieria de Reactores Nucleares, Paseo Cuauhnahuac 8532, 62550 Jiutepec, Mor. (Mexico); Espinosa-Paredes, Gilberto [Area de Ingenieria en Recursos Energeticos, Universidad Autonoma Metropolitana, Avenida San Rafael Atlixco 186, Col. Vicentina, 09340 Mexico, D.F. (Mexico)

    2005-04-15

    This paper is concerned with the design of a boiling water reactor (BWR) equilibrium core using thorium as a nuclear material in an integrated blanket-seed (BS) assembly. The integrated BS concept comes from the fact that the blanket and the seed rods are located in the same assembly, and are burned out in a once-through cycle. The idea behind the lattice design is to use the thorium conversion capability in a BWR spectrum, taking advantage of the {sup 233}U build-up. A core design was developed to achieve an equilibrium cycle of 365 effective full power days in a standard BWR with a reload of 104 fuel assemblies designed with an average {sup 235}U enrichment of 7.5 w/o in the seed sub-lattice. The main operating parameters, like power, linear heat generation rate and void distributions were obtained as well as the shutdown margin. It was observed that the analyzed parameters behave like those obtained in a standard BWR. The shutdown margin design criterion was fulfilled by addition of a burnable poison region in the fuel assembly.

  13. Behavior and Distribution of Heavy Metals Including Rare Earth Elements, Thorium, and Uranium in Sludge from Industry Water Treatment Plant and Recovery Method of Metals by Biosurfactants Application

    Science.gov (United States)

    Gao, Lidi; Kano, Naoki; Sato, Yuichi; Li, Chong; Zhang, Shuang; Imaizumi, Hiroshi

    2012-01-01

    In order to investigate the behavior, distribution, and characteristics of heavy metals including rare earth elements (REEs), thorium (Th), and uranium (U) in sludge, the total and fractional concentrations of these elements in sludge collected from an industry water treatment plant were determined and compared with those in natural soil. In addition, the removal/recovery process of heavy metals (Pb, Cr, and Ni) from the polluted sludge was studied with biosurfactant (saponin and sophorolipid) elution by batch and column experiments to evaluate the efficiency of biosurfactant for the removal of heavy metals. Consequently, the following matters have been largely clarified. (1) Heavy metallic elements in sludge have generally larger concentrations and exist as more unstable fraction than those in natural soil. (2) Nonionic saponin including carboxyl group is more efficient than sophorolipid for the removal of heavy metals in polluted sludge. Saponin has selectivity for the mobilization of heavy metals and mainly reacts with heavy metals in F3 (the fraction bound to carbonates) and F5 (the fraction bound to Fe-Mn oxides). (3) The recovery efficiency of heavy metals (Pb, Ni, and Cr) reached about 90–100% using a precipitation method with alkaline solution. PMID:22693485

  14. Evaluations of Radionuclides of Uranium, Thorium, and Radium Associated with Produced Fluids, Precipitates, and Sludges from Oil, Gas, and Oilfield Brine Injection Wells in Mississippi

    Energy Technology Data Exchange (ETDEWEB)

    Ericksen, R.L.

    1999-10-28

    There is an unsurpassed lack of scientific data with respect to the concentrations and isotopic compositions of uranium, thorium, and radium in the produced formation fluids (brine), precipitates, and sludges generated with the operation of oil and gas wells in Mississippi. These radioactive elements when contained in the formation fluids have been given the term NORM, which is an acronym for naturally occurring radioactive materials. When they are technologically enhanced during oil and gas production activities resulting in the formation of scale (precipitates) and sludges they are termed TENORM (technologically enhanced naturally occurring radioactive materials). As used in this document, NORM and TENORM will be considered equivalent terms and the occurrence of NORM in the oilfield will be considered the result of production operations. As a result of the lack of data no scientifically sound theses may be developed concerning the presence of these radionuclides in the fluid brine, precipitate (scale), or sludge phases. Over the period of just one year, 1997 for example, Mississippi produced over 39,372,963,584 liters (10,402,368,186 gallons or 247,675,433 barrels) of formation water associated with hydrocarbon production from 41 counties across the state.

  15. ALPHA SPECTROMETRIC EVALUATION OF SRM-995 AS A POTENTIAL URANIUM/THORIUM DOUBLE TRACER SYSTEM FOR AGE-DATING URANIUM MATERIALS

    Energy Technology Data Exchange (ETDEWEB)

    Beals, D.

    2011-12-06

    Uranium-233 (t{sub 1/2} {approx} 1.59E5 years) is an artificial, fissile isotope of uranium that has significant importance in nuclear forensics. The isotope provides a unique signature in determining the origin and provenance of uranium-bearing materials and is valuable as a mass spectrometric tracer. Alpha spectrometry was employed in the critical evaluation of a {sup 233}U standard reference material (SRM-995) as a dual tracer system based on the in-growth of {sup 229}Th (t{sub 1/2} {approx} 7.34E3 years) for {approx}35 years following radiochemical purification. Preliminary investigations focused on the isotopic analysis of standards and unmodified fractions of SRM-995; all samples were separated and purified using a multi-column anion-exchange scheme. The {sup 229}Th/{sup 233}U atom ratio for SRM-995 was found to be 1.598E-4 ({+-} 4.50%) using recovery-corrected radiochemical methods. Using the Bateman equations and relevant half-lives, this ratio reflects a material that was purified {approx} 36.8 years prior to this analysis. The calculated age is discussed in contrast with both the date of certification and the recorded date of last purification.

  16. Design of an equilibrium nucleus of a BWR type reactor based in a Thorium-Uranium fuel; Diseno de un nucleo de equilibrio de un reactor tipo BWR basado en un combustible de Torio-Uranio

    Energy Technology Data Exchange (ETDEWEB)

    Francois, J.L.; Nunez C, A. [Laboratorio de Analisis en Ingenieria de Reactores Nucleares, Facultad de Ingenieria-UNAM, Paseo Cuauhnahuac 8532, Jiutepec, Morelos (Mexico)

    2003-07-01

    In this work the design of the reactor nucleus of boiling water using fuel of thorium-uranium is presented. Starting from an integral concept based in a type cover-seed assemble is carried out the design of an equilibrium reload for the nucleus of a reactor like that of the Laguna Verde Central and its are analyzed some of the main design variables like the cycle length, the reload fraction, the burnt fuel, the vacuum distribution, the generation of lineal heat, the margin of shutdown, as well as a first estimation of the fuel cost. The results show that it is feasible to obtain an equilibrium reload, comparable to those that are carried out in the Laguna Verde reactors, with a good behavior of those analyzed variables. The cost of the equilibrium reload designed with the thorium-uranium fuel is approximately 2% high that the uranium reload producing the same energy. It is concluded that it is convenient to include burnable poisons, type gadolinium, in the fuel with the end of improving the reload design, the fuel costs and the margin of shutdown. (Author)

  17. Thorium and Uranium Hydride Phosphorus and Arsenic Bearing Molecules with Single and Double Actinide-Pnictogen and Bridged Agostic Hydrogen Bonds.

    Science.gov (United States)

    Andrews, Lester; Cho, Han-Gook; Thanthiriwatte, K Sahan; Dixon, David A

    2017-03-06

    Thorium atoms from laser ablation react with phosphine during condensation in excess argon to produce two new infrared absorptions at 1467.2 and 1436.6 cm(-1) near weak bands for ThH and ThH2, which increase on annealing to 25 and 30 K, indicating spontaneous reactions. Analogous experiments with uranium produced two similar bands at 1473.4 and 1456.7 cm(-1) above UH at 1423.8 cm(-1) and another absorption at 1388.2 cm(-1). Electronic structure calculations at the coupled cluster CCSD(T) for Th and density functional theory calculations for U as well as their proximity to other actinide hydride absorptions support assignments of these bands to the simplest molecules HP═ThH2, HP═UH2, and PH2-UH. Arsine gave the analogous products HAs═ThH2, HAs═UH2, and AsH2-UH. The HE═AnH2 molecules (E = P, As; An = Th, U) have strong agostic An-H(E) interactions with H-E-An angles in the range of 60-64°. The calculated agostic bond distances are 9% to 12% longer than terminal single An-H bonds, which suggests that these strong agostic bonds can be considered as bridge bonds since similar relationships are found for the dibridged M2H6 molecules (M = Al, Ga, In). The NBO analysis and the molecular orbitals show the presence of a σ and a π bond for HE═AnH2 molecules that are heavily polarized with most of the density on the P or As.

  18. Advanced Proliferation Resistant, Lower Cost, Uranium-Thorium Dioxide Fuels for Light Water Reactors (Progress report for work through June 2002, 12th quarterly report)

    Energy Technology Data Exchange (ETDEWEB)

    Mac Donald, Philip Elsworth

    2002-09-01

    The overall objective of this NERI project is to evaluate the potential advantages and disadvantages of an optimized thorium-uranium dioxide (ThO2/UO2) fuel design for light water reactors (LWRs). The project is led by the Idaho National Engineering and Environmental Laboratory (INEEL), with the collaboration of three universities, the University of Florida, Massachusetts Institute of Technology (MIT), and Purdue University; Argonne National Laboratory; and all of the Pressurized Water Reactor (PWR) fuel vendors in the United States (Framatome, Siemens, and Westinghouse). In addition, a number of researchers at the Korean Atomic Energy Research Institute and Professor Kwangheon Park at Kyunghee University are active collaborators with Korean Ministry of Science and Technology funding. The project has been organized into five tasks: · Task 1 consists of fuel cycle neutronics and economics analysis to determine the economic viability of various ThO2/UO2 fuel designs in PWRs, · Task 2 will determine whether or not ThO2/UO2 fuel can be manufactured economically, · Task 3 will evaluate the behavior of ThO2/UO2 fuel during normal, off-normal, and accident conditions and compare the results with the results of previous UO2 fuel evaluations and U.S. Nuclear Regulatory Commission (NRC) licensing standards, · Task 4 will determine the long-term stability of ThO2/UO2 high-level waste, and · Task 5 consists of the Korean work on core design, fuel performance analysis, and xenon diffusivity measurements.

  19. Assessment of the solubility of thorium and uranium from black sand of Camargue in both simulated lung and gut fluids for dose calculation after internal exposure

    Energy Technology Data Exchange (ETDEWEB)

    Frelon, S.; Chazel, V.; Tourlonias, E.; Paquet, F. [IRSN/ DRPH/ SRBE, LRTOX, BP 166, 26702 Pierrelatte Cedex (France); Blanchardon, E. [IRSN/ DRPH/ SDI, LEDI, BP 17, 92262 Fontenay Aux Roses Cedex (France); Bouisset, P. [IRSN/ DEI/ STEME, LMRE, Bois des rames, 91400 Orsay (France); Pourcelot, L. [IRSN/ DEI/ SESURE, LERCM, BP3, 13 115 St Paul lez Durance Cedex (France)

    2006-07-01

    In the south of France, some beaches of Camargue present a high rate of natural radioactivity due to thorium and uranium from zircon and apatite heavy minerals present in the so-called black sand. These radionuclides may lead to internal exposure consecutive to inhalation or ingestion of this sand. The accurate assessment of radiological risk after internal exposure of public frequenting these beaches requires some information on the human bioavailability of U and Th from the sand. Both routes of intake were studied in this work and the consecutive dose delivered was calculated under two different scenarios for each type of exposure. As far as inhalation is concerned, the first important conclusion is that the inhalable fraction, i.e. particles with aerodynamic diameters below 50 {mu}m, was tiny (0.002%) in this sample of sand. Moreover in vitro assays of solubility were performed for this fraction and showed that U and Th as well as their progeny presented moderate solubility. Then effective doses under several scenarios were calculated and seem to demonstrate a very poor risk of exposure after inhalation. Indeed, a dose of 1 mSv would be received by a babies after inhalation of about 40 Kg of sand, that is impossible, whereas a more realistic scenario of chronic exposure only reached 31 {mu} Sv. In case of ingestion, the solubility of Th and U in the gastrointestinal fluids was found to be very low with a maximum solubility of 0.5% of the initial mass of radioelement in the sample of sand. Then the worst hypothesis studied yields an effective dose of 0.018 mSv./(g-swallowed sand) that is roughly 50 times less than the legal annual dose limit for members of the public. as a conclusion, the possible internal dose after exposure by inhalation or ingestion of black sand of Camargue seems to be very low under the conditions of this study. (N.C.)

  20. Determination of plutonium-239, thorium-232, and natural uranium isotopic concentrations in biological samples using photofission track analysis

    Science.gov (United States)

    Parry, James Roswell

    Fission track analysis (FTA) has many uses in the scientific community including but not limited to geological dating, neutron flux mapping, and dose reconstruction. The common method of fission for FTA is through neutrons from a nuclear reactor. This dissertation investigates the use of bremsstrahlung radiation produced from an electron linear accelerator to induce fission in FTA samples. This provides a means of simultaneously measuring the amount of Pu-239, U-nat, and Th-232 in a single sample. The benefit of measuring the three isotopes simultaneously is the possible elimination of costly and time consuming chemical processing for dose reconstruction samples. Samples containing the three isotopes were irradiated in two different bremsstrahlung spectra and a neutron spectrum to determine the amount of Pu-239, U-nat, and Th-232 in the samples. The reaction rate from the calibration samples and the counted fission tracks on the samples were used in determining the concentration of each isotope in the samples. The results were accurate to within a factor of two or three, showing that the method can work to predict the concentrations of multiple isotopes in a sample. The limitations of current accelerators and detectors limits the application of this specific procedure to higher concentrations of isotopes. The method detection limits for Pu-239, U-nat, and Th-232 are 20 pCi, 1 fCi, and 0.4 flCI respectively. Analysis of extremely low concentrations of isotopes would require the use of different detectors such as quartz due to the embrittlement encountered in the Lexan at high exposures. Cracking of the Texan detectors started to appear at a fluence of about 2 x 1018 electrons from the accelerator. This may be partly due to the beam stop not being an adequate thickness. The procedure is likely limited to specialty applications for the near term. However, with the world concerns of exposure to depleted uranium, this procedure may find applications in this area since

  1. Simultaneous determination of Ra-226, natural uranium and natural thorium by gamma-ray spectrometry INa(Ti), in solid samples.; Determinacion de U (Natural), Th (Natural) y Ra-226 en diversos materiales, mediante espectrometria con INa (TI)

    Energy Technology Data Exchange (ETDEWEB)

    Salvador, S.; Navarro, T.; Alvarez, A.

    1991-07-01

    A method has been developed to determine activities of Ra-226, natural uranium and natural thorium by gamma-ray spectrometry. The measurement system has been calibrated using standards specially prepared at the laboratory. It is necessary to assume secular equilibrium in the samples, between Ra-226 and Th-232 and its daughters nuclides, and between U-238 and its immediate daughter Th-234, as the photo peaks measured are those of the daughters. The results obtained indicate that this method can of ter replace the radiochemical techniques used to measure activities in this type of sample. The method has been successfully used to determine these natural isotopes in samples from uranium mills. (Author) 9 refs.

  2. Proceedings of the 9. international conference on health effects of incorporated radionuclides emphasis on radium, thorium, uranium and their daughter products - HEIR 2004

    Energy Technology Data Exchange (ETDEWEB)

    Oeh, U.; Roth, P.; Paretzke, H.G. (eds.) [GSF - Forschungszentrum fuer Umwelt und Gesundheit GmbH, Neuherberg (Germany)

    2005-07-01

    The ninth international conference on 'Health Effects of Incorporated Radionuclides - Emphasis on Radium, Thorium, Uranium and their Daughter Products' HEIR 2004 was held at GSF-National Research Center for Environment and Health, Neuherberg, Germany, from November 29 until December 1, 2004. The growing popularity of this topic among the scientific community, especially the radiation protection community, was demonstrated by the largest number of participants in comparison to the earlier conferences. In all, there were 157 participants from 20 different countries of the world. In the conference 62 scientific and 12 poster presentations were included in 13 sessions. The scope of the conference covered studies related to the long-term follow-up of thorotrast subjects in Japan, Germany and Portugal, and also of the subjects exposed to Ra-224 for the treatment of bone tuberculosis and ankylosing spondylitis. The studies and discussions on these topics are important in view of the large number of liver cancers observed in the thorotrast patients and the number of bone cancers in the cases treated with Ra-224. A growth stunting was also observed for the subjects who received the Ra-224 injections early in their lives. Besides atom bomb survivors, the data from thorotrast patients could well help towards a better understanding of the health effects of irradiations. In addition to the scientific presentations on the above topics, there were a number of presentations on the incidence of lung cancer from radon exposure of miners and plutonium exposures causing lung cancer among the Mayak workers in the Russian Federation. Other stimulating presentations were on the tissue damaging mechanisms of alpha particles, having very high L.E.T., and also the related radiation weighting factor in comparison to beta and gamma radiations. There were also interesting presentations on the topics of uncertainties involved in the internal dose assessment from radiation exposure and

  3. Thorium Energy for the World

    CERN Document Server

    Revol, Jean-Pierre; Bourquin, Maurice; Kadi, Yacine; Lillestol, Egil; De Mestral, Jean-Christophe; Samec, Karel

    2016-01-01

    The Thorium Energy Conference (ThEC13) gathered some of the world’s leading experts on thorium technologies to review the possibility of destroying nuclear waste in the short term, and replacing the uranium fuel cycle in nuclear systems with the thorium fuel cycle in the long term. The latter would provide abundant, reliable and safe energy with no CO2 production, no air pollution, and minimal waste production. The participants, representatives of 30 countries, included Carlo Rubbia, Nobel Prize Laureate in physics and inventor of the Energy Amplifier; Jack Steinberger, Nobel Prize Laureate in physics; Hans Blix, former Director General of the International Atomic Energy Agency (IAEA); Rolf Heuer, Director General of CERN; Pascal Couchepin, former President of the Swiss Confederation; and Claude Haegi, President of the FEDRE, to name just a few. The ThEC13 proceedings are a source of reference on the use of thorium for energy generation. They offer detailed technical reviews of the status of thorium energy ...

  4. 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.

  5. Thorium-uranium fission radiography

    Science.gov (United States)

    Haines, E. L.; Weiss, J. R.; Burnett, D. S.; Woolum, D. S.

    1976-01-01

    Results are described for studies designed to develop routine methods for in-situ measurement of the abundance of Th and U on a microscale in heterogeneous samples, especially rocks, using the secondary high-energy neutron flux developed when the 650 MeV proton beam of an accelerator is stopped in a 42 x 42 cm diam Cu cylinder. Irradiations were performed at three different locations in a rabbit tube in the beam stop area, and thick metal foils of Bi, Th, and natural U as well as polished silicate glasses of known U and Th contents were used as targets and were placed in contact with mica which served as a fission track detector. In many cases both bare and Cd-covered detectors were exposed. The exposed mica samples were etched in 48% HF and the fission tracks counted by conventional transmitted light microscopy. Relative fission cross sections are examined, along with absolute Th track production rates, interaction tracks, and a comparison of measured and calculated fission rates. The practicality of fast neutron radiography revealed by experiments to data is discussed primarily for Th/U measurements, and mixtures of other fissionable nuclei are briefly considered.

  6. Safety and Regulatory Issues of the Thorium Fuel Cycle

    Energy Technology Data Exchange (ETDEWEB)

    Ade, Brian [ORNL; Worrall, Andrew [ORNL; Powers, Jeffrey [ORNL; Bowman, Steve [ORNL; Flanagan, George [ORNL; Gehin, Jess [ORNL

    2014-02-01

    Thorium has been widely considered an alternative to uranium fuel because of its relatively large natural abundance and its ability to breed fissile fuel (233U) from natural thorium (232Th). Possible scenarios for using thorium in the nuclear fuel cycle include use in different nuclear reactor types (light water, high temperature gas cooled, fast spectrum sodium, molten salt, etc.), advanced accelerator-driven systems, or even fission-fusion hybrid systems. The most likely near-term application of thorium in the United States is in currently operating light water reactors (LWRs). This use is primarily based on concepts that mix thorium with uranium (UO2 + ThO2), add fertile thorium (ThO2) fuel pins to LWR fuel assemblies, or use mixed plutonium and thorium (PuO2 + ThO2) fuel assemblies. The addition of thorium to currently operating LWRs would result in a number of different phenomenological impacts on the nuclear fuel. Thorium and its irradiation products have nuclear characteristics that are different from those of uranium. In addition, ThO2, alone or mixed with UO2 fuel, leads to different chemical and physical properties of the fuel. These aspects are key to reactor safety-related issues. The primary objectives of this report are to summarize historical, current, and proposed uses of thorium in nuclear reactors; provide some important properties of thorium fuel; perform qualitative and quantitative evaluations of both in-reactor and out-of-reactor safety issues and requirements specific to a thorium-based fuel cycle for current LWR reactor designs; and identify key knowledge gaps and technical issues that need to be addressed for the licensing of thorium LWR fuel in the United States.

  7. Correlation of radioactive waste treatment costs and the environmental impact of waste effluents in the nuclear fuel cycle: fabrication of high-temperature gas-cooled reactor fuel containing uranium-233 and thorium

    Energy Technology Data Exchange (ETDEWEB)

    Roddy, J.W.; Blanco, R.E.; Hill, G.S.; Moore, R.E.; Seagren, R.D.; Witherspoon, J.P.

    1976-06-01

    A cost/benefit study was made to determine the cost and effectiveness of various radioactive waste (radwaste) treatment systems for decreasing the release of radioactive materials from model High-Temperature Gas-Cooled (HTGR) fuel fabrication plants and to determine the radiological impact (dose commitment) of the released materials on the environment. The study is designed to assist in defining the term ''as low as reasonably achievable'' as it applies to these nuclear facilities. The base cases of the two model plants, a fresh fuel fabrication plant and a refabrication plant, are representative of current proposed commercial designs or are based on technology that is being developed to fabricate uranium, thorium, and graphite into fuel elements. The annual capacities of the fresh fuel plant and the refabrication plant are 450 and 245 metric tons of heavy metal (where heavy metal is uranium plus thorium), as charged to about fifty 1000-MW(e) HTGRs. Additional radwaste treatment systems are added to the base case plants in a series of case studies to decrease the amounts of radioactive materials released and to reduce the radiological dose commitment to the population in the surrounding area. The capital and annual costs for the added waste treatment operations and the corresponding reductions in dose commitments are calculated for each case. In the final analysis, the cost/benefit of each case, calculated as additional cost of radwaste system divided by the reduction in dose commitment, is tabulated or the dose commitment is plotted with cost as the variable. The status of each of the radwaste treatment methods is discussed. 48 figures, 74 tables.

  8. Study Of Thorium As A Nuclear Fuel.

    Directory of Open Access Journals (Sweden)

    Prakash Humane

    2017-10-01

    Full Text Available Conventional fuel sources for power generation are to be replacing by nuclear power sources like nuclear fuel Uranium. But Uranium-235 is the only fissile fuel which is in 0.72 found in nature as an isotope of Uranium-238. U-238 is abundant in nature which is not fissile while U-239 by alpha decay naturally converted to Uranium- 235. For accompanying this nuclear fuel there is another nuclear fuel Thorium is present in nature is abundant can be used as nuclear fuel and is as much as safe and portable like U-235.

  9. Uranium in granites from the Southwestern United States: actinide parent-daughter systems, sites and mobilization. First year report

    Energy Technology Data Exchange (ETDEWEB)

    Silver, L T; Williams, I S; Woodhead, J A

    1980-10-01

    Some of the principal findings of the study on the Lawler Peak Granite are: the granite is dated precisely by this work at 1411 +- 3 m.y., confirming its synchroneity with a great regional terrane of granites. Uranium is presently 8-10 times crustal abundance and thorium 2-3 times in this granite. Uranium is found to be enriched in at least eight, possibly ten, primary igneous mineral species over the whole-rock values. Individual mineral species show distinct levels in, and characteristics ranges of, uranium concentration. It appears that in a uraniferous granite such as this, conventional accuracy mineral suites probably cannot account for most of the uranium in the rock, and more rare, high U-concentration phases also are present and are significant uranium hosts. It appears that at least two different geological episodes have contributed to the disturbance of the U-Th-Pb isotope systems. Studies of various sites for transient dispersal of uranium, thorium, and radiogenic lead isotopes indicate a non-uniform dispersal of these components. It appears that the bulk rock has lost at least 24 percent of its original uranium endowment, accepting limited or no radiogenic lead or thorium migration from the sample.

  10. Thorium: An energy source for the world of tomorrow

    Directory of Open Access Journals (Sweden)

    Revol J.-P.

    2015-01-01

    Full Text Available To meet the tremendous world energy needs, systematic R&D has to be pursued to replace fossil fuels. Nuclear energy, which produces no green house gases and no air pollution, should be a leading candidate. How nuclear energy, based on thorium rather than uranium, could be an acceptable solution is discussed. Thorium can be used both to produce energy and to destroy nuclear waste. The thorium conference, organized by iThEC at CERN in October 2013, has shown that thorium is seriously considered by some major developing countries as a key element of their energy strategy. However, developed countries do not seem to move fast enough in that direction, while global cooperation is highly desirable in this domain. Thorium is not fissile. Various possible ways of using thorium will be reviewed. However, an elegant option is to drive an “Accelerator Driven System (ADS” with a proton accelerator, as suggested by Nobel Prize laureate Carlo Rubbia .

  11. Towards an intrinsically safe and economic thorium breeder reactor

    Energy Technology Data Exchange (ETDEWEB)

    Jagannathan, V. [Light Water Reactor Physics Section, Reactor Physics Design Division, Bhabha Atomic Research Centre, 5th Floor, Central Complex, Mumbai 400085 (India)]. E-mail: vjagan@magnum.barc.ernet.in; Pal, Usha [Light Water Reactor Physics Section, Reactor Physics Design Division, Bhabha Atomic Research Centre, 5th Floor, Central Complex, Mumbai 400085 (India)

    2006-10-15

    Thorium does not have intrinsic fissile content unlike uranium. {sup 232}Th has nearly three times thermal absorption cross section compared to {sup 238}U and hence requires much larger externally fed fissile content compared to uranium based fuel. These factors give a permanent economic competitive edge to uranium. Thus thorium is not inducted in any significant measure in present day power reactors, despite the fact that thorium is three times more abundant in the earth's crust than uranium. Uranium reserves vary from country to country and there is also difficulty in having equitable distribution of uranium. Thus when {sup 235}U would get exhausted, perhaps much sooner in countries having limited uranium reserve, there will be a need to switch over from the today's open fuel cycle programme based on {sup 235}U feed to closed fuel cycle based on Pu feed. At that stage thorium and (depleted) uranium would become equal candidates to form the fertile base. All economic considerations would have to be readdressed. The size and growth of the nuclear power programme based on closed fuel cycle would be dependent on maximizing the fissile conversion rate in those reactors. In this paper we reemphasize the principles and the details of the thermal reactor concept 'A Thorium Breeder Reactor' (ATBR), in which the use of PuO{sub 2} seeded thoria fuel is found to give excellent core characteristics like two years cycle length with nearly zero control maneuvers, fairly high seed output to input ratio and intrinsically safe reactivity coefficients [Jagannathan V, Ganesan S, Karthikeyan R. Sensitivity studies for a thorium breeder reactor design with the nuclear data libraries of WIMS library update project. In: Proceedings of the international conference on emerging nuclear energy systems ICENES-2000, September 25-28, 2000, Petten, The Netherlands].

  12. 10 CFR 40.28 - General license for custody and long-term care of uranium or thorium byproduct materials disposal...

    Science.gov (United States)

    2010-01-01

    ... 10 Energy 1 2010-01-01 2010-01-01 false General license for custody and long-term care of uranium... COMMISSION DOMESTIC LICENSING OF SOURCE MATERIAL General Licenses § 40.28 General license for custody and... issued for the custody of and long-term care, including monitoring, maintenance, and emergency measures...

  13. Radionuclide Basics: Thorium

    Science.gov (United States)

    Thorium is a naturally occurring radioactive metal found at trace levels in soil, rocks, plants and animals. Thorium is used very little in industry, but can be found in heat-resistant alloys and paints and optical lenses.

  14. Neutron- and proton-induced nuclear data evaluation of thorium, uranium and curium isotopes for energies up to 250 MeV

    CERN Document Server

    Young, Ouk Lee; Jonghwa, Chang; Konobeyev, A Yu

    2004-01-01

    The evaluation of neutron- and proton nuclear data for thorium-232, U-233,234,236, and Cm-243,244,245,246 isotopes have been performed at energies up to 250 MeV. Neutron data was evaluated at energies from 20 MeV to 250 MeV, and combined with the JENDL-3.3 data at 20 MeV while proton data was obtained for energies from 1 to 250 MeV. Nuclear model parameters are largely based on the IAEA-RIPL recommendation, and adjusted to better reproduce the available measurements. The coupled channel optical model was applied to calculate the total, reaction, elastic, and direct inelastic cross sections, and to obtain the transmission coefficients. Decay of excited nuclei was described with the Hauser-Feshbach and exciton models using the GNASH code to simultaneously handle neutron, proton, deuteron, triton, helium-3, alpha , gamma emissions and fissions. Special attention was paid on the fission cross sections for energies where experimental data are scant, using appropriate systematics and fittings. Particles and gamma e...

  15. Uranium, radium and thorium in soils with high-resolution gamma spectroscopy, MCNP-generated efficiencies, and VRF non-linear full-spectrum nuclide shape fitting

    OpenAIRE

    Metzger Robert; Riper Kenneth Van; Lasche George

    2017-01-01

    A new method for analysis of uranium and radium in soils by gamma spectroscopy has been developed using VRF (“Visual RobFit”) which, unlike traditional peak-search techniques, fits full-spectrum nuclide shapes with non-linear least-squares minimization of the chi-squared statistic. Gamma efficiency curves were developed for a 500 mL Marinelli beaker geometry as a function of soil density using MCNP. Collected spectra were then analyzed using the MCNP-generated efficiency curves and VRF to dec...

  16. Uranium-238 and thorium-232 series concentrations in soil, radon-222 indoor and drinking water concentrations and dose assessment in the city of Alameda, Chihuahua, Mexico

    Energy Technology Data Exchange (ETDEWEB)

    Colmenero Sujo, L.; Montero Cabrera, M.E. E-mail: elena.montero@cimav.edu.mx; Villalba, L.; Renteria Villalobos, M.; Torres Moye, E.; Garcia Leon, M.; Garcia-Tenorio, R.; Mireles Garcia, F.; Herrera Peraza, E.F.; Sanchez Aroche, D

    2004-07-01

    High-resolution gamma spectrometry was used to determine the concentration of {sup 40}K, {sup 238}U and {sup 232}Th series in soil samples taken from areas surrounding the city of Aldama, in Chihuahua. Results of indoor air short-time sampling, with diffusion barrier charcoal detectors, revealed relatively high indoor radon levels, ranging from 29 to 422 Bq/m{sup 3}; the radon concentrations detected exceeded 148 Bq/m{sup 3} in 76% of the homes tested. Additionally, liquid scintillation counting showed concentrations of radon in drinking water ranging from 4.3 to 42 kBq/m{sup 3}. The high activity of {sup 238}U in soil found in some places may be a result of the uranium milling process performed 20 years ago in the area. High radon concentrations indoor and in water may be explained by assuming the presence of uranium-bearing rocks underneath of the city, similar to a felsic dike located near Aldama. The estimated annual effective dose of gamma radiation from the soil and radon inhalation was 3.83 mSv.

  17. Raman Spectroscopy for Analysis of Thorium Compounds

    Energy Technology Data Exchange (ETDEWEB)

    Su, Yin-Fong; Johnson, Timothy J.; Olsen, Khris B.

    2016-05-12

    The thorium fuel cycle is an alternative to the uranium fuel cycle in that when 232Th is irradiated with neutrons it is converted to 233U, another fissile isotope. There are several chemical forms of thorium which are used in the Th fuel cycle. Recently, Raman spectroscopy has become a very portable and facile analytical technique useful for many applications, including e.g. determining the chemical composition of different materials such as for thorium compounds. The technique continues to improve with the development of ever-more sensitive instrumentation and better software. Using a laboratory Fourier-transform (FT)-Raman spectrometer with a 785 nm wavelength laser, we were able to obtain Raman spectra from a series of thorium-bearing compounds of unknown origin. These spectra were compared to the spectra of in-stock-laboratory thorium compounds including ThO2, ThF4, Th(CO3)2 and Th(C2O4)2. The unknown spectra showed very good agreement to the known standards, demonstrating the applicability of Raman spectroscopy for detection and identification of these nuclear materials.

  18. Thorium impact on tobacco root transcriptome

    Czech Academy of Sciences Publication Activity Database

    Mazari, Kateřina; Landa, Přemysl; Přerostová, Sylva; Müller, Karel; Vaňková, Radomíra; Soudek, Petr; Vaněk, Tomáš

    2017-01-01

    Roč. 325 (2017), s. 163-169 ISSN 0304-3894 R&D Projects: GA MŠk(CZ) LD11073; GA MŠk(CZ) LD13029 Institutional support: RVO:61389030 Keywords : arabidopsis-thaliana roots * juncea var. foliosa * cadmium accumulation * deficiency responses * mineral-nutrition * gene-expression * plant transfer * iron uptake * uranium * soil * Microarray * Thorium * Gene expression * Toxicity * Nicotiana tabacum Subject RIV: ED - Physiology Impact factor: 6.065, year: 2016

  19. Thorium dioxide: properties and nuclear applications

    Energy Technology Data Exchange (ETDEWEB)

    Belle, J.; Berman, R.M. (eds.)

    1984-01-01

    This is the sixth book on reactor materials published under sponsorship of the Naval Reactors Office of the United States Department of Energy, formerly the United States Atomic Energy Commission. This book presents a comprehensive compilation of the most significant properties of thorium dioxide, much like the book Uranium Dioxide: Properties and Nuclear Applications presented information on the fuel material used in the Shippingport Pressurized Water Reactor core.

  20. A review on the status of development in thorium-based nuclear fuels

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Young Woo; Na, S. H.; Lee, Y. W.; Kim, H. S.; Kim, S. H.; Joung, C.Y

    2000-02-01

    Thorium as an alternative nuclear energy source had been widely investigated in the 1950s-1960s because it is more abundant than uranium, but the studies of thorium nuclear fuel cycle were discontinued by political and economic reasons in the 1970s. Recently, however, renewed interest was vested in thorium-based nuclear fuel cycle because it may generate less long-lived minor actinides and has a lower radiotoxicity of high level wastes after reprocessing compared with the thorium fuel cycle. In this state-of the art report, thorium-based nuclear cycle. In this state-of the art report, thorium-based nuclear fuel cycle and fuel fabrication processes developed so far with different reactor types are reviewed and analyzed to establish basic technologies of thorium fuel fabrication which could meet our situation. (author)

  1. THORIUM DISPERSION IN BISMUTH

    Science.gov (United States)

    Bryner, J.S.

    1961-07-01

    The growth of thorium bismutaide particles, which are formed when thorium is suspended in liquid bismuth, is inhibited when the liquid metal suspension is being flowed through a reactor and through a heat exchanger in sequence. It involves the addition of as little as 1 part by weight of tellurium to 100 parts of thorium. This addition is sufficient to inhibit particle growth and agglomeration.

  2. LWR First Recycle of TRU with Thorium Oxide for Transmutation and Cross Sections

    Energy Technology Data Exchange (ETDEWEB)

    Andrea Alfonsi; Gilles Youinou

    2012-07-01

    Thorium has been considered as an option to uranium-based fuel, based on considerations of resource utilization (thorium is approximately three times more plentiful than uranium) and as a result of concerns about proliferation and waste management (e.g. reduced production of plutonium, etc.). Since the average composition of natural Thorium is dominated (100%) by the fertile isotope Th-232, Thorium is only useful as a resource for breeding new fissile materials, in this case U-233. Consequently a certain amount of fissile material must be present at the start-up of the reactor in order to guarantee its operation. The thorium fuel can be used in both once-through and recycle options, and in both fast and thermal spectrum systems. The present study has been aimed by the necessity of investigating the option of using reprocessed plutonium/TRU, from a once-through reference LEU scenario (50 GWd/ tIHM), mixed with natural thorium and the need of collect data (mass fractions, cross-sections etc.) for this particular fuel cycle scenario. As previously pointed out, the fissile plutonium is needed to guarantee the operation of the reactor. Four different scenarios have been considered: • Thorium – recycled Plutonium; • Thorium – recycled Plutonium/Neptunium; • Thorium – recycled Plutonium/Neptunium/Americium; • Thorium – recycled Transuranic. The calculations have been performed with SCALE6.1-TRITON.

  3. LWR First Recycle of TRU with Thorium Oxide for Transmutation and Cross Sections

    Energy Technology Data Exchange (ETDEWEB)

    Andrea Alfonsi; Gilles Youinou; Sonat Sen

    2013-02-01

    Thorium has been considered as an option to uranium-based fuel, based on considerations of resource utilization (thorium is approximately three times more plentiful than uranium) and as a result of concerns about proliferation and waste management (e.g. reduced production of plutonium, etc.). Since the average composition of natural Thorium is dominated (100%) by the fertile isotope Th-232, Thorium is only useful as a resource for breeding new fissile materials, in this case U-233. Consequently a certain amount of fissile material must be present at the start-up of the reactor in order to guarantee its operation. The thorium fuel can be used in both once-through and recycle options, and in both fast and thermal spectrum systems. The present study has been aimed by the necessity of investigating the option of using reprocessed plutonium/TRU, from a once-through reference LEU scenario (50 GWd/ tIHM), mixed with natural thorium and the need of collect data (mass fractions, cross-sections etc.) for this particular fuel cycle scenario. As previously pointed out, the fissile plutonium is needed to guarantee the operation of the reactor. Four different scenarios have been considered: • Thorium – recycled Plutonium; • Thorium – recycled Plutonium/Neptunium; • Thorium – recycled Plutonium/Neptunium/Americium; • Thorium – recycled Transuranic. The calculations have been performed with SCALE6.1-TRITON.

  4. Recognition of favorable zones for uranium and thorium accumulation, at Um Ara-Um Shilman granitic pluton, south eastern desert, Egypt, using airborne spectrometric and magnetic data

    Energy Technology Data Exchange (ETDEWEB)

    Elkattan, E.M. [Nuclear Materials Authority, Cairo (Egypt)

    1995-06-01

    The objective is aimed at identifying significant U and Th anomalies, the amount of re-mobilization of U and Th, the structural framework of the granite pluton and the distribution of spectrometric anomalies. The study revealed that the granite pluton could be represented as a single radio-lithologic unit excluding abnormal measurements exceeding Xban + 2S. It also revealed the existence of eight strong spectrometric anomalies. Observed values of eU correlate well with eTh, r=0.72 while the correlation between eU/eTh and eU is lacking, r=0.190. Meanwhile, there is a negative correlation between eU/eTh and eTh,r= -0.335. This deficiency in correlation suggests a limited or zero remobilization of uranium, which was partly governed by magmatic processes. Most of the radioactive anomalies were found within or near the major contact faults which may act as channels for mineralized fluids from the subsurface. These fluids possess increased concentrations of U and/or Th which could exist in appropriate chemical and/or structural traps. The U and Th anomalies were found to be associated with the northern and southern parts of the granite pluton respectively. The difference between the northern and southern parts of the granite pluton may be attributed to differences in radioelement content, the effect of partial and/or complete digestion of older rocks, or to different levels of erosion. (author).

  5. Dynamic Analysis of the Thorium Fuel Cycle in CANDU Reactors

    Energy Technology Data Exchange (ETDEWEB)

    Jeong, Chang Joon; Park, Chang Je

    2006-02-15

    The thorium fuel recycle scenarios through the Canada deuterium uranium (CANDU) reactor have been analyzed for two types of thorium fuel: homogeneous ThO{sub 2}UO{sub 2} and ThO{sub 2}UO{sub 2}-DUPIC fuels. The recycling is performed through the dry process fuel technology which has a proliferation resistance. For the once-through fuel cycle model, the existing nuclear power plant construction plan was considered up to 2016, while the nuclear demand growth rate from the year 2016 was assumed to be 0%. After setting up the once-through fuel cycle model, the thorium fuel CANDU reactor was modeled to investigate the fuel cycle parameters. In this analysis, the spent fuel inventory as well as the amount of plutonium, minor actinides and fission products of the multiple recycling fuel cycle were estimated and compared to those of the once-through fuel cycle. From the analysis results, it was found that the closed or partially closed thorium fuel cycle can be constructed through the dry process technology. Also, it is known that both the homogeneous and heterogeneous thorium fuel cycles can reduce the SF accumulation and save the natural uranium resource compared with the once-through cycle. From the material balance view point, the heterogeneous thorium fuel cycle seems to be more feasible. It is recommended, however, the economic analysis should be performed in future.

  6. Thorium as a Fuel for Accelerator Driven Subcritical Electronuclear Systems

    CERN Document Server

    Barashenkov, V S; Singh, V

    2000-01-01

    Neutron yield and energy production in a very large, practically infinite, uranium and thorium target-blocks irradiated by protons with energies in the range 0.1-2 GeV are studied by Monte Carlo method. Though the comparison of uranium and thorium targets shows that the neutron yield in the latter is 30-40 % less and the energy gain is approximatelly two times smaller, accelerator Driven subcritical Systems (ADS) with thorium fuel are very perspective at the bombarding energies higher than several hundreds MeV. An admixture of fissile elements U^{233}, U^{235}, Pu^{239} in the set-up gives larger neutron multiplication which in turn shows better energy amplification. It is argued that due to the practically complete burning of the fuel in such set-up there is no need of technology of conversion of the exhaust fuel.

  7. Comparison of the reactivity of 2-Li-C{sub 6}H{sub 4}CH{sub 2}NMe{sub 2} with MCl{sub 4} (M=Th, U). Isolation of a thorium aryl complex or a uranium benzyne complex

    Energy Technology Data Exchange (ETDEWEB)

    Seaman, Lani A.; Pedrick, Elizabeth A.; Wu, Guang; Hayton, Trevor W. [California Univ., Santa Barbara, CA (United States). Dept. of Chemistry and Biochemistry; Tsuchiya, Takashi; Jakubikova, Elena [North Carolina State Univ., Raleigh, NC (United States). Dept. of Chemistry

    2013-09-27

    Individualism under actinoids: The reaction of 2-Li-C{sub 6}H{sub 4}CH{sub 2}NMe{sub 2} with [MCl{sub 4} (dme) {sub n}] (M=Th, n=2; M=U, n=0) gives the thorium aryl complex [Th(2-C{sub 6}H{sub 4}CH{sub 2}NMe{sub 2}){sub 4}] or the uranium benzene complex Li[U(2,3-C{sub 6}H{sub 3}CH{sub 2}NMe{sub 2})(2-C{sub 6}H{sub 4}CH{sub 2}NMe{sub 2}){sub 3}]. A DFT analysis suggests that the formation of a benzyne complex with uranium but not with thorium is a kinetic and not thermodynamic effect. [German] Individualismus unter Actinoiden: Die Reaktion von 2-Li-C{sub 6}H{sub 4}CH{sub 2}NMe{sub 2} mit [MCl{sub 4} (dme) {sub n}] (M=Th, n=2; M=U, n=0) ergibt den Thoriumarylkomplex [Th(2-C{sub 6}H{sub 4}CH{sub 2}NMe{sub 2}){sub 4}] bzw. den Uranbenz-inkomplex Li[U(2,3-C{sub 6}H{sub 3}CH{sub 2}NMe{sub 2})(2-C{sub 6}H{sub 4}CH{sub 2}NMe{sub 2}){sub 3}]. Einer dichtefunktionaltheoretischen Analyse zufolge ist es kinetisch und nicht thermodynamisch bedingt, dass der Benz-inkomplex im Fall von Uran entsteht, nicht aber im Fall von Thorium.

  8. CATALYTIC RECOMBINATION OF RADIOLYTIC GASES IN THORIUM OXIDE SLURRIES

    Science.gov (United States)

    Morse, L.E.

    1962-08-01

    A method for the coinbination of hydrogen and oxygen in aqueous thorium oxide-uranium oxide slurries is described. A small amount of molybdenum oxide catalyst is provided in the slurry. This catalyst is applicable to the recombination of hydrogen and/or deuterium and oxygen produced by irradiation of the slurries in nuclear reactors. (AEC)

  9. Radiochemical separation of thorium 234 from uranile acetylacetonate

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Rendon, R.M.; Solache, R.M.; Tenorio, D. (Instituto Nacional de Investigaciones Nucleares, Mexico City)

    1984-03-15

    The optimum conditions for the chemical separation of thorium compounds obtained by the chemical effects of ..cap alpha.. decay of uranium 238, in uranile acetylacetonate were established. The separation technique used was solvent extraction; the retention value obtained was 9.8+-2.1%.

  10. Uranium-thorium-protactinium dating systematics

    Science.gov (United States)

    Cheng, H.; Edwards, R. Lawrence; Murrell, M. T.; Benjamin, T. M.

    1998-11-01

    With precise 234U, 230Th, and 231Pa data available, 230Th and 231Pa ages can now be tested rigorously for concordancy. If the material is not concordant, the isotopic characteristics of this material may be examined in some detail. Here, models similar to those used to describe the U-Pb system are evaluated for use in U-Th-Pa studies, for the case in which initial 230Th and 231Pa concentrations are effectively zero. The systematics of concordia plots in relation to models of variation in δ 234U, episodic U loss or gain, continuous U loss or gain, and continuous 234U, 230Th and 231Pa gain or loss are considered for the case in which initial U concentration is significant (for example, in many carbonate deposits). We also examine linear U uptake models for the case in which initial U concentration is effectively zero (for example, in teeth and bones). Such models should prove useful in interpreting data from materials that have behaved as open-systems. In particular, these models may help constrain the nature of diagenetic processes, and in some situations it may be possible to determine or constrain true ages with materials that have behaved as open-systems.

  11. Self-Sustaining Thorium Boiling Water Reactors

    Directory of Open Access Journals (Sweden)

    Ehud Greenspan

    2012-10-01

    Full Text Available A thorium-fueled water-cooled reactor core design approach that features a radially uniform composition of fuel rods in stationary fuel assembly and is fuel-self-sustaining is described. This core design concept is similar to the Reduced moderation Boiling Water Reactor (RBWR proposed by Hitachi to fit within an ABWR pressure vessel, with the following exceptions: use of thorium instead of depleted uranium for the fertile fuel; elimination of the internal blanket; and elimination of absorbers from the axial reflectors, while increasing the length of the fissile zone. The preliminary analysis indicates that it is feasible to design such cores to be fuel-self-sustaining and to have a comfortably low peak linear heat generation rate when operating at the nominal ABWR power level of nearly 4000 MWth. However, the void reactivity feedback tends to be too negative, making it difficult to have sufficient shutdown reactivity margin at cold zero power condition. An addition of a small amount of plutonium from LWR used nuclear fuel was found effective in reducing the magnitude of the negative void reactivity effect and enables attaining adequate shutdown reactivity margin; it also flattens the axial power distribution. The resulting design concept offers an efficient incineration of the LWR generated plutonium in addition to effective utilization of thorium. Additional R&D is required in order to arrive at a reliable practical and safe design.

  12. Thorium as an energy source. Opportunities for Norway

    Energy Technology Data Exchange (ETDEWEB)

    2008-01-15

    Final Recommendations of the Thorium Report Committee: 1) No technology should be idolized or demonized. All carbon-dioxide (Co2) emission-free energy production technologies should be considered. The potential contribution of nuclear energy to a sustainable energy future should be recognized. 2) An investigation into the resources in the Fen Complex and other sites in Norway should be performed. It is essential to assess whether thorium in Norwegian rocks can be defined as an economical asset for the benefit of future generations. Furthermore, the application of new technologies for the extraction of thorium from the available mineral sources should be studied. 3) Testing of thorium fuel in the Halden Reactor should be encouraged, taking benefit of the well recognized nuclear fuel competence in Halden. 4) Norway should strengthen its participation in international collaborations by joining the EURATOM fission program and the GIF program on Generation IV reactors suitable for the use of thorium. 5) The development of an Accelerator Driven System (ADS) using thorium is not within the capability of Norway working alone. Joining the European effort in this field should be considered. Norwegian research groups should be encouraged to participate in relevant international projects, although these are currently focused on waste management. 6) Norway should bring its competence in waste management up to an international standard and collaboration with Sweden and Finland could be beneficial. 7) Norway should bring its competence with respect to dose assessment related to the thorium cycle up to an international standard. 8) Since the proliferation resistance of uranium-233 depends on the reactor and reprocessing technologies, this aspect will be of key concern should any thorium reactor be built in Norway. 9) Any new nuclear activities in Norway, e.g. thorium fuel cycles, would need strong international pooling of human resources, and in the case of thorium, a strong long

  13. Dosimetry evaluation of the potential exposure bound to uranium and thorium natural accumulation in the sand of some beaches of the Camargue littoral; Evaluations dosimetriques de l'exposition potentielle liee a l'accumulation naturelle d'uranium et de thorium dans les sables de certaines plages du littoral de Camargue

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2007-07-01

    The aim of this report is the assessment of potential exposure to radioactive sands discovered in 2000 in two points of the coast of the Camargue (East of Beauduc and Espiguette lighthouses), where specific activity can reach up several thousands of Bq.kg{sup -1} for radionuclides of U{sup 238} and Th{sup 232} radioactive families, and environmental dose rate up to ten times of usual natural background. The excess of radioactivity is carried by small particles of sand (apatites and zircons less than 100 {mu}m). First chapter focuses on radioactivity of the coast of the Golfe du lion and of the Camargue, and more particularly on these two points (cartography, measure, radionuclide identification, mineralogical characterization of particles). This chapter concludes the excess of radioactivity is natural; particles come from several massifs of the Rhone basin, transported by the river and re-distributed on the coast. Second chapter focuses on dosimetric assessment, using reasonable scenarios for the frequenting of these sites by persons of the public in one hand, and drawing up the sizing of the sands and their solubility in gastric and intestinal fluids in an other hand. the annual effective dose, carefully calculated, is about 1 mSv, mainly due to external exposure to gamma rays. such a dose, of same levels as the dose received for 17 months of residence in Paris for example, does not involve any particular action. (authors)

  14. TRU Recycling in Thorium Fuel Cycle of PWR with various moderator-to-fuel volume ratio

    Energy Technology Data Exchange (ETDEWEB)

    Waris, Abdul; Su' ud, Zaki; Kurniadi, Rizal [Institut Teknologi Bandung, Jl. Ganesa No. 10, Bandung, West Java 40132 (Indonesia)

    2009-06-15

    Global attention to proliferation resistance has increased and as a result advanced nuclear core and fuel designs are required to possess a high level of proliferation resistance. Thorium fuel is well recognized for its inherently high proliferation resistance potential because of the low production rates of plutonium and minor actinides as compared with uranium fuel. Thorium has less radio-toxicity of spent fuel and also displays a good breeding ratio in thermal reactors. Therefore, study on thorium-based nuclear fuels has become interesting again. It is believed that by using a modern thorium-based fuel design in current reactor, a better economic performance can be achieved [1, 2]. Thorium can be utilized as fuel in nuclear reactors like uranium even though thorium is not fissile material, since {sup 232}Th is capable to capture thermal neutrons to produce {sup 233}U, a fissile isotope. Therefore, the common thorium fuel consists of {sup 232}Th and {sup 233}U for initial loading fuel. For this reason we need a thorium breeder to realize the thorium fuel reactor system, since {sup 233}U does not occur naturally. As a part of revisiting the thorium-based nuclear fuel for the present and future nuclear energy system, the present study focuses on analysis of trans-uranium (TRU) recycling in thorium fuel cycle of pressurized water reactor (PWR) to overcome the need of thorium breeder. PWR was chosen since it will still dominate the nuclear energy system up to 2050. For comprehensive study, an influence of moderator-to-fuel volume ratio (MFR) changes by changing the pin-pitch of fuel cell is also evaluated. The MFR ranges from 0.5 to 4.0. The result show that the standard PWR with MFR = 2.0 may be a good design for TRU recycling in thorium fuel cycle. The complete results will be given in the full paper. References: [1] A. Waris, H. Sekimoto and G. Kastchiev (2002), Influence of Moderator-to-Fuel Volume Ratio on Pu and MA Recycling in Equilibrium Fuel Cycle of PWR

  15. METHOD OF SEPARATING URANIUM VALUES, PLUTONIUM VALUES AND FISSION PRODUCTS BY CHLORINATION

    Science.gov (United States)

    Brown, H.S.; Seaborg, G.T.

    1959-02-24

    The separation of plutonium and uranium from each other and from other substances is described. In general, the method comprises the steps of contacting the uranium with chlorine in the presence of a holdback material selected from the group consisting of lanthanum oxide and thorium oxide to form a uranium chloride higher than uranium tetrachloride, and thereafter heating the uranium chloride thus formed to a temperature at which the uranium chloride is volatilized off but below the volatilizalion temperature of plutonium chloride.

  16. Recovery of thorium and rare earths by their peroxides precipitation from a residue produced in the thorium purification facility; Recuperacao de torio e terras raras via peroxido do residuo originado na unidade de purificacao de torio

    Energy Technology Data Exchange (ETDEWEB)

    Freitas, Antonio Alves de

    2008-07-01

    As consequence of the operation of a Thorium purification facility, for pure Thorium Nitrate production, the IPEN (Instituto de Pesquisas Energeticas e Nucleares) has stored away a solid residue called RETOTER (REsiduo de TOrio e TErras Raras). The RETOTER is rich in Rare-Earth Elements and significant amount of Thorium-232 and minor amount of Uranium. Furthermore it contains several radionuclides from the natural decay series. Significant radioactivity contribution is generated by the Thorium descendent, mainly the Radium-228(T{sub 1/2}=5.7y), known as meso thorium and Thorium-228(T{sub 1/2} 1.90y). An important thorium daughter is the Lead-208, a stable isotope present with an expressive quantity. After the enclosure of the operation of the Thorium purification facility, many researches have been developed for the establishment of methodologies for recovery of Thorium, Rare-Earth Elements and Lead-208 from the RETOTER. This work presents a method for RETOTER decontamination, separating and bordering upon some radioactive isotopes. The residue was digested with nitric acid and the Radium-228 was separated by the Barium Sulphate co-precipitation procedure. Finally, the Thorium was separated by the peroxide precipitation and the Rare-Earth Elements were also recovered by the Rare-Earth peroxide precipitation in the filtrate solution.(author)

  17. Elaboration of thorium uranium phosphate-diphosphate({beta}-TUPD) and {beta}-TUPD/monazite composite materials from crystallized precursors: sintering and study of the long term behavior of the ceramics; Elaboration de phosphate-diphosphate de thorium et d'uranium ({beta}-PDTU) et de materiaux composites {beta}-PDTU/Monazite a partir de precurseurs cristallises. Etudes du frittage et de la durabilite chimique

    Energy Technology Data Exchange (ETDEWEB)

    Clavier, N

    2004-11-01

    Thorium Phosphate-Diphosphate ({beta}-TPD) is actually considered as potential host matrix for the immobilization of radionuclides, and especially actinides, in the field of an underground repository. The studies reported in this work are based on the precipitation of the Thorium Phosphate Hydrogen-Phosphate Hydrate (TPHPH) as a precursor of {beta}-TPD. The crystal structure of TPHPH was solved then the reactions involved during its transformation into {beta}-TPD were established. It allows us to put in evidence a new monoclinic variety of TPD, called {alpha}-TPD, acting as intermediate of reaction. Moreover, the existence of a complete solid solution between TPHPH and UPHPH was demonstrated.The experimental conditions of sintering leading to an optimal densification of the pellets were determined. The relative density of the samples was always between 95 and 100% of the calculated value while a significant improvement of the homogeneity of the samples was noted. By this way, the process based on the precipitation of low-temperature crystallized precursors followed by their heat treatment at high temperature was applied to the preparation of {beta}-TUPD/Monazite based composites in the aim to incorporate simultaneously tri- and tetravalent actinides. The chemical durability of {beta}-TUPD sintered samples was evaluated. The normalized leaching rates determined in several experimental conditions revealed the good resistance of the solids to aqueous alteration. Moreover, the normalized dissolution rates exhibited a low dependence to temperature, pH as well as to several ions present in the leachate. For all the samples, thorium was quickly precipitated as a neo-formed phosphate phase identified to TPHPH. (author)

  18. Thorium-based fuel cycles: Reassessment of fuel economics and proliferation risk

    Energy Technology Data Exchange (ETDEWEB)

    Serfontein, Dawid E., E-mail: Dawid.Serfontein@nwu.ac.za [Senior Lecturer at the School of Mechanical and Nuclear Engineering, North West University (PUK-Campus), PRIVATE BAG X6001, Internal Post Box 360, Potchefstroom 2520 (South Africa); Mulder, Eben J. [Professor at the School of Mechanical and Nuclear Engineering, North West University (South Africa)

    2014-05-01

    At current consumption and current prices, the proven reserves for natural uranium will last only about 100 years. However, the more abundant thorium, burned in breeder reactors, such as large High Temperature Gas-Cooled Reactors, and followed by chemical reprocessing of the spent fuel, could stretch the 100 years for uranium supply to 15,000 years. Thorium-based fuel cycles are also viewed as more proliferation resistant compared to uranium. However, several barriers to entry caused all countries, except India and Russia, to abandon their short term plans for thorium reactor projects, in favour of uranium/plutonium fuel cycles. In this article, based on the theory of resonance integrals and original analysis of fast fission cross sections, the breeding potential of {sup 232}Th is compared to that of {sup 238}U. From a review of the literature, the fuel economy of thorium-based fuel cycles is compared to that of natural uranium-based cycles. This is combined with a technical assessment of the proliferation resistance of thorium-based fuel cycles, based on a review of the literature. Natural uranium is currently so cheap that it contributes only about 10% of the cost of nuclear electricity. Chemical reprocessing is also very expensive. Therefore conservation of natural uranium by means of the introduction of thorium into the fuel is not yet cost effective and will only break even once the price of natural uranium were to increase from the current level of about $70/pound yellow cake to above about $200/pound. However, since fuel costs constitutes only a small fraction of the total cost of nuclear electricity, employing reprocessing in a thorium cycle, for the sake of its strategic benefits, may still be a financially viable option. The most important source of the proliferation resistance of {sup 232}Th/{sup 233}U fuel cycles is denaturisation of the {sup 233}U in the spent fuel by {sup 232}U, for which the highly radioactive decay chain potentially poses a large

  19. High resolution analysis of uranium and thorium concentration as well as U-series isotope distributions in a Neanderthal tooth from Payre (Ardèche, France) using laser ablation ICP-MS

    Science.gov (United States)

    Grün, Rainer; Aubert, Maxime; Joannes-Boyau, Renaud; Moncel, Marie-Hélène

    2008-11-01

    We have mapped U ( 238U) and Th ( 232Th) elemental concentrations as well as U-series isotope distributions in a Neanderthal tooth from the Middle Palaeolithic site of Payre using laser ablation ICP-MS. The U-concentrations in an enamel section varied between 1 and 1500 ppb. The U-concentration maps show that U-migration through the external enamel surface is minute, the bulk of the uranium having migrated internally via the dentine into the enamel. The uranium migration and uptake is critically dependent on the mineralogical structure of the enamel. Increased U-concentrations are observed along lineaments, some of which are associated with cracks, and others may be related to intra-prismatic zones or structural weaknesses reaching from the dentine into the enamel. The uranium concentrations in the dentine vary between about 25,000 and 45,000 ppb. Our systematic mapping of U-concentration and U-series isotopes provides insight into the time domain of U-accumulation. Most of the uranium was accumulated in an early stage of burial, with some much later overprints. None of the uranium concentration and U-series profiles across the root of the tooth complied with a single stage diffusion-adsorption (D-A) model that is used for quality control in U-series dating of bones and teeth. Nevertheless, in the domains that yielded the oldest apparent U-series age estimates, U-leaching could be excluded. This means that the oldest apparent U-series ages of around 200 ka represent a minimum age for this Neanderthal specimen. This is in good agreement with independent age assessments (200-230 ka) for the archaeological layer, in which it was found. The Th elemental concentrations in the dental tissues were generally low (between about 1 and 20 ppb), and show little relationship with the nature of the tissue.

  20. Multiparametric study of thorium oxide dissolution in aqueous media

    Energy Technology Data Exchange (ETDEWEB)

    Simonnet, Marie; Barre, Nicole; Drot, Romuald; Le Naour, Claire; Sladkov, Vladimir; Delpech, Sylvie [Universite Paris-Saclay, CNRS-IN2P3, Orsay (France). Institut de Physique Nucleaire

    2016-07-01

    Thorium oxide is poorly soluble: unlike uranium oxide, concentrated nitric acid medium is not sufficient to get quantitative dissolution. Addition of small amounts of fluoride is required to achieve thorium oxide total dissolution. The effect of several parameters on thorium oxide dissolution in order to optimize the dissolution conditions is reported in this paper. Thus the influence of solid characteristics, dissolution method, temperature and composition of dissolution medium on ThO{sub 2} dissolution rate has been studied. No complexing agents tested other than fluoride allows total dissolution. Beyond a given HF concentration a decrease of the dissolution rate is observed due to the formation of a precipitate at the solid/solution interface. It was demonstrated by XPS measurements that this precipitate is constituted of thorium fluoride (ThF{sub 4}) formed during the ThO{sub 2} dissolution. The low concentration of HF required to achieve a total dissolution and the activation energy value measured tends to show a catalytic effect of HF on the dissolution process.

  1. Geological and geochemical aspects of uranium deposits. A selected, annotated bibliography

    Energy Technology Data Exchange (ETDEWEB)

    Garland, P.A.; Thomas, J.M.; Brock, M.L.; Daniel, E.W. (comps.)

    1980-06-01

    A bibliography of 479 references encompassing the fields of uranium and thorium geochemistry and mineralogy, geology of uranium deposits, uranium mining, and uranium exploration techniques has been compiled by the Ecological Sciences Information Center of Oak Ridge National Laboratory. The bibliography was produced for the National Uranium Resource Evaluation Program, which is funded by the Grand Junction Office of the Department of Energy. The references contained in the bibliography have been divided into the following eight subject categories: (1) geology of deposits, (2) geochemistry, (3) genesis O deposits, (4) exploration, (5) mineralogy, (6) uranium industry, (7) reserves and resources, and (8) geology of potential uranium-bearing areas. All categories specifically refer to uranium and thorium; the last category contains basic geologic information concerning areas which the Grand Junction Office feels are particularly favorable for uranium deposition. The references are indexed by author, geographic location, quadrangle name, geoformational feature, taxonomic name, and keyword.

  2. Thorium nuclear fuel cycle technology

    Energy Technology Data Exchange (ETDEWEB)

    Eom, Tae Yoon; Do, Jae Bum; Choi, Yoon Dong; Park, Kyoung Kyum; Choi, In Kyu; Lee, Jae Won; Song, Woong Sup; Kim, Heong Woo

    1998-03-01

    Since thorium produces relatively small amount of TRU elements after irradiation in the reactor, it is considered one of possible media to mix with the elements to be transmuted. Both solid and molten-salt thorium fuel cycles were investigated. Transmutation concepts being studied involved fast breeder reactor, accelerator-driven subcritical reactor, and energy amplifier with thorium. Long-lived radionuclides, especially TRU elements, could be separated from spent fuel by a pyrochemical process which is evaluated to be proliferation resistance. Pyrochemical processes of IFR, MSRE and ATW were reviewed and evaluated in detail, regarding technological feasibility, compatibility of thorium with TRU, proliferation resistance, their economy and safety. (author). 26 refs., 22 figs

  3. Anticipated radiological impacts from the mining and milling of thorium for the nonproliferative fuels. [Dose commitments to individuals and populations from inhalation or ingestion of thorium-cycle-related radionuclides

    Energy Technology Data Exchange (ETDEWEB)

    Meyer, H. R.; Till, J. E.

    1978-01-01

    Recent emphasis on proliferation-resistant fuel cycles utilizing thorium--uranium-233 fuels has necessitated evaluation of the potential radiological impact of mining and milling thorium ore. Therefore, an analysis has been completed of hypothetical mine-mill complexes using population and meteorological data representative of a thorium resource site in the Lemhi Pass area of Idaho/Montana, United States of America. Source terms for the site include thorium-232 decay chain radionuclides suspended as dusts and radon-220 and daughters initially released as gas. Fifty-year dose commitments to maximally exposed individuals of 2.4 mrem to total body, 9.5 mrem to bone, and 35 mrem to lungs are calculated to result from facility operation. Radium-228, thorium-228, thorium-232 and lead-212 (daughter of radon-220) are found to be the principal contributors to dose. General population doses for a 50-mile radius surrounding the facility are estimated to be 0.05 man-rem to total body, 0.1 man-rem to bone, and 0.7 man-rem to lungs. Generally speaking, the results of this study indicate that the radiological aspects of thorium mining and milling should pose no significant problems with regard to implementation of thorium fuel cycles.

  4. Contributions to the geology of uranium and thorium by the United States Geological Survey and Atomic Energy Commission for the United Nations International Conference on Peaceful Uses of Atomic Energy, Geneva, Switzerland, 1955

    Science.gov (United States)

    Page, Lincoln R.; Stocking, Hobart E.; Smith, Harriet B.

    1956-01-01

    Within the boundaries of the United States abnormal amounts of uranium have been found in rocks of nearly all geologic ages and lithologic types. Distribution of ore is more restricted. On the Colorado Plateau, the Morrison formation of Jurassic age yields 61.4 percent of the ore produced in the United States, and the Chinle conglomerate and Shinarump formation of Triassic age contribute 26.0 and 5.8 percent, respectively. Clastic, carbonaceous, and carbonate sedimentary rocks of Tertiary, Mesozoic, and Paleozoic ages and veins of Tertiary age are the source of the remaining 6.8 percent.

  5. Simulation on reactor TRIGA Puspati core kinetics fueled with thorium (Th) based fuel element

    Science.gov (United States)

    Mohammed, Abdul Aziz; Pauzi, Anas Muhamad; Rahman, Shaik Mohmmed Haikhal Abdul; Zin, Muhamad Rawi Muhammad; Jamro, Rafhayudi; Idris, Faridah Mohamad

    2016-01-01

    In confronting global energy requirement and the search for better technologies, there is a real case for widening the range of potential variations in the design of nuclear power plants. Smaller and simpler reactors are attractive, provided they can meet safety and security standards and non-proliferation issues. On fuel cycle aspect, thorium fuel cycles produce much less plutonium and other radioactive transuranic elements than uranium fuel cycles. Although not fissile itself, Th-232 will absorb slow neutrons to produce uranium-233 (233U), which is fissile. By introducing Thorium, the numbers of highly enriched uranium fuel element can be reduced while maintaining the core neutronic performance. This paper describes the core kinetic of a small research reactor core like TRIGA fueled with a Th filled fuel element matrix using a general purpose Monte Carlo N-Particle (MCNP) code.

  6. Determination of thorium in plutonium-thorium oxides and carbides

    Energy Technology Data Exchange (ETDEWEB)

    Walker, L.F.; Temer, D.J.

    1979-10-01

    Thorium is determined in (PuTh)C and (PuTh)O/sub 2/ by complexometric titration with ethylenediaminetetraacetic acid (EDTA) following separation on anion-exchange resin. Carbides are first oxidized by ignition in air at about 800/sup 0/C. Oxide or oxidized carbide samples are dissolved in acids by the sealed-reflux technique or by heating in beakers. The plutonium is selectively sorbed from the 12M hydrochloric acid solution of the fuel on a Bio-Rad AG1-X2 anion-exchange resin column, and the eluted thorium is titrated with EDTA using xylenol orange as the indicator. The average recovery of thorium in 20 samples is 99.98% with a relative standard deviation of 0.07%.

  7. Determination of the equivalent doses due to the ingestion of radionuclides from the uranium and thorium series presents in drinking waters of the region of Santa Luzia, Paraiba state, Brazil; Determinacao das doses equivalentes devido a ingestao de radionuclideos das series do uranio e torio presentes em aguas de consumo do municipio de Santa Luzia, estado da Paraiba

    Energy Technology Data Exchange (ETDEWEB)

    Pastura, Valeria F. da S., E-mail: vpastura@cnen.gov.b [Comissao Nacional de Energia Nuclear (DRSN/CNEN), Rio de Janeiro, RJ (Brazil). Diretoria de Radioprotecao e Seguranca Nuclear. Coordenacao de Materias Primas e Minerais; Campos, Thomas F. da C.; Petta, Reinaldo A., E-mail: thomascampos@geologia.ufrn.b, E-mail: petta@geologia.ufrn.b [Universidade Federal do Rio Grande do Norte (LARANA/UFRN), Natal, RN (Brazil). Lab. de Radioatividade Natural

    2011-10-26

    This paper determined the original dose equivalents from radionuclides of uranium and thorium series in a drinking water of well which is supplied to the population of Santa Luzia, Paraiba state, Brazil. The collected waters are near to the mineralized phlegmatic bodies in rose quartz and amazonite feldspar. Radiometric measurements performed on the feldspar vein point out counting ratios surrounding 30000 cps and the analysis of collected samples of minerals presented tenors for the {sup 226}Ra and {sup 219}Pb varying from 0.50 to 2.30 Bq/sw. For determination of concentration of radionuclides U{sub Total}, {sup 226}Ra, {sup 228}Ra and {sup 219}Pb, found in the not desalinated, two methods were used, spectrophotometry with arsenazo and radiochemistry, both realized in the CNEN-LAPOC laboratories. For the calculation of dose equivalent it was taken into consideration the following parameters: the dose coefficients for incorporation by ingestion for public individuals with ages over 17 years (Norma CNEN-NN-3.01, Regulatory Position 3.01/011) and daily ingestion of 4 liters of water, which is over the recommended by the WHO of 2L/day - 1993. The obtained values were compared with the reference value for compromised dose equivalent established by WHO for evaluate the risk potential to the health of population, by ingestion. The radionuclide concentrations in the wells varies from 0.054 to 0.21 Bq/L, resulting dose equivalents of 3.94 x 10{sup -3} mSv/year and 0.17 mSv/year in the studied population

  8. Radiochemical separation of thorium acetylacetonate from other thorium species

    Energy Technology Data Exchange (ETDEWEB)

    Solache Rios, M.; Tenorio, D.

    1987-01-16

    A solvent extraction technique to separate different chemical species of thorium is presented. The products formed by the chemical effects of the (n,el) reaction on the Th(acac)/sub 4/ were separated by this method and the retention value was measured. 6 refs.

  9. Thorium Energy Resources and its Potential of Georgian Republic, The Caucasus

    Science.gov (United States)

    Gogoladze, Salome; Okrostsvaridze, Avtandil

    2017-04-01

    Energy resources, currently consumed by modern civilization, are represented by hydrocarbons - 78-80 %, however these reserves are exhausting. In light of these challenges, search of new energy resources is vital importance problem for the modern civilization. Based on the analysis of existing energy reserves and potential, as the main energy resources for the future of our civilization, the renewable and nuclear energy should be considered. However, thorium has a number of advantages compared to Uranium (Kazimi, 2003; et al.): It is concentrated in the earth crust 4-5 times more than uranium; extraction and enrichment of thorium is much cheaper than uranium's; It is less radioactive; complete destruction of its waste products is possible; thorium yields much more energy than uranium. Because of unique properties and currently existed difficult energetic situation thorium is considered as the main green energy resource in the 3rd millennium of the human civilization (Martin, 2009). Georgia republic, which is situated in the central part of Caucasus, poor of hydrocarbons, but has a thorium resource important potential. In general the Caucasus represents a collisional orogen, that formed along the Eurasian North continental margin and extends over 1200 km from Caspian to Black Sea. Three major units are distinguished in its construction: the Greater and Lesser Caucasian mobile belts and the Transcaucasus microplate. Currently it represents the Tethyan segment connecting the Mediterranean and Iran-Himalayan orogenic belts, between the Gondvana-derived Arabian plate and East European platform. Now in Georgian Republic are marked thorium four ore occurrences (Okrostsvaridze, 2014): 1- in the Sothern slope of the Greater Caucasus, in the quartz -plagioclases veins (Th concentrations vary between 51g/t - 3882 g/t); 2- in the Transcaucasus Dzirula massif hydrothermally altered rocks of the Precambrian quartz-diorite gneisses (Th concentrations vary between 117 g/t -266 g

  10. Integral experiments on thorium assemblies with D-T neutron source

    Directory of Open Access Journals (Sweden)

    Liu Rong

    2017-01-01

    Full Text Available To validate nuclear data and code in the neutronics design of a hybrid reactor with thorium, integral experiments in two kinds of benchmark thorium assemblies with a D-T fusion neutron source have been performed. The one kind of 1D assemblies consists of polyethylene and depleted uranium shells. The other kind of 2D assemblies consists of three thorium oxide cylinders. The capture reaction rates, fission reaction rates, and (n, 2n reaction rates in 232Th in the assemblies are measured by ThO2 foils. The leakage neutron spectra from the ThO2 cylinders are measured by a liquid scintillation detector. The experimental uncertainties in all the results are analyzed. The measured results are compared to the calculated ones with MCNP code and ENDF/B-VII.0 library data.

  11. Integral experiments on thorium assemblies with D-T neutron source

    Science.gov (United States)

    Liu, Rong; Yang, Yiwei; Feng, Song; Zheng, Lei; Lai, Caifeng; Lu, Xinxin; Wang, Mei; Jiang, Li

    2017-09-01

    To validate nuclear data and code in the neutronics design of a hybrid reactor with thorium, integral experiments in two kinds of benchmark thorium assemblies with a D-T fusion neutron source have been performed. The one kind of 1D assemblies consists of polyethylene and depleted uranium shells. The other kind of 2D assemblies consists of three thorium oxide cylinders. The capture reaction rates, fission reaction rates, and (n, 2n) reaction rates in 232Th in the assemblies are measured by ThO2 foils. The leakage neutron spectra from the ThO2 cylinders are measured by a liquid scintillation detector. The experimental uncertainties in all the results are analyzed. The measured results are compared to the calculated ones with MCNP code and ENDF/B-VII.0 library data.

  12. Evaluation of U-Zr hydride fuel for a thorium fuel cycle in an RTR concept

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Kyung Taek; Cho, Nam Zin [Korea Advanced Institute of Science and Technology, Taejon (Korea, Republic of)

    1998-12-31

    In this paper, we performed a design study of a thorium fueled reactor according to the design concept of the Radkowsky Thorium Reactor (RTR) and evaluated its overall performance. To enhance its performance and alleviate its problems, we introduced a new metallic uranium fuel, uranium-zirconium hydride (U-ZrH{sub 1.6}), as a seed fuel. For comparison, typical ABB/CE-type PWR based on SYSTEM 80+and standard RTR-type thorium reactor were also studied. From the results of performance analysis, we could ascertain advantages of RTR-type thorium fueled reactor in proliferation resistance, fuel cycle economics, and back-end fuel cycle. Also, we found that enhancement of proliferation resistance and safer operating conditions may be achieved by using the U-ZrH{sub 1.6} fuel in the seed region without additional penalties in comparison with the standard RTR`s U-Zr fuel. 6 refs., 2 figs., 6 tabs. (Author)

  13. A novel biamperometric methodology for thorium determination by EDTA complexometric titration

    Energy Technology Data Exchange (ETDEWEB)

    Jayachandran, K.; Gamare, J.S.; Nair, P.R.; Xavier, M.; Aggarwal, S.K. [Bhabha Atomic Reseach Centre, Mumbai (India). Fuel Chemistry Div.

    2012-07-01

    A biamperometric methodology is described for the determination of thorium by EDTA complexometric titration, based on the observed electrochemical behaviour of EDTA when the applied potential was {>=} 200 mV between the twin Pt electrodes. Studies carried out showed that a pH range of 2.4-2.7 was optimum for the determination. Accuracy and precision of the method were evaluated using different amounts of thorium ranging from 50 {mu}g to 5 mg. Studies on the interference of uranium were carried out with different amounts of uranium ranging from 20 to 80% using the presently developed approach of biamperometry as well as the conventional indicator method. The method was employed for the determination of Th in (Th,U)O{sub 2} samples containing different amounts of Th and U. (orig.)

  14. The Thorium-Cycle: safe, abundant power for the new millennium

    Science.gov (United States)

    Don, May; George, Kim; Peter, Mcintyre; Charles, Meitzler; Robert, Rogers; Akhdior, Sattarov; Mustafa, Yavuz

    2001-10-01

    A design has been developed for using accelerator-driven thorium fission to produce electric power. A thorium-cycle reactor works by electro-breeding. A pattern of thorium fuel rods is supported in a vessel containing molten lead. A beam of high-energy (1 GeV) protons is targeted in the center of the vessel, and produces a copious flux of energetic neutrons by spallation. The neutrons transmute the thorium nuclei two steps up the periodic table to U233, which fissions rapidly to produce thermal energy. The lead serves as the spallation target, the moderator, and the heat exchange medium to transfer heat from the core to steam exchangers above the core. The thorium cycle has several important advantages over current uranium-cycle fission technology: it is intrinsically stable it cannot melt down; it eats its own waste; it cannot produce bomb-grade isotopes; and there are sufficient thorium reserves to supply the entire Earth’s energy economy for the next millennium. The concept of a thorium-cycle power reactor was first proposed by Rubbia in 1995. Key problems in the original concept were the proton injector (15 MW beam power), reliability of accelerator systems, and parasitic absorption of neutrons by fission products during the life of the core. We have addressed all three problems in a design for a flux-coupled stack of isochronous cyclotrons, delivering a pattern of 7 independent beams to the core. An interdisciplinary collaboration is being formed to develop the concept to a serious design.

  15. Spectrophotometric study of the thorium-morin mixed-color system

    Science.gov (United States)

    Fletcher, M.H.; Milkey, R.G.

    1956-01-01

    A spectrophotometric study was made of the thoriummorin reaction to evaluate the suitability of morin as a reagent for the determination of trace amounts of thorium. At pH 2, the equilibrium constant for the reaction is 1 ?? 106, and a single complex having a thorium-morin ratio of 1 to 2 is formed. The complex shows maximum absorbance at a wave length of 410 m??, and its absorbance obeys Beer's law. The absorbance readings are highly reproducible, and the sensitivity is relatively high, an absorbance difference of 0.001 being equivalent to 0.007 ?? of ThO2 per sq. cm. The effects of acid, alcohol, and morin concentration, time, temperature, and age of the morin reagent as well as the behavior of morin with zirconium(IV), iron(III), aluminum(III), ytterbium(III), yttrium(III), uranium(VI), praseodymium(III), lead(II), lanthanum(III), and calcium(II) ions are discussed. A method is presented for the determination of thorium in pure solutions. Appropriate separations for the isolation of thorium may extend the usefulness of the method and permit the determination of trace amounts of thorium in complex materials.

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

    Energy Technology Data Exchange (ETDEWEB)

    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 {sup 234}U/{sup 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 {sup 222}Rn to {sup 234}U in solution, corrected for weathering, to infer the retardation factor for uranium. Similar methods could be applied to thorium and radium.

  17. National Uranium Resource Evaluation. Volume 1. Summary of the geology and uranium potential of Precambrian conglomerates in southeastern Wyoming

    Energy Technology Data Exchange (ETDEWEB)

    Karlstrom, K.E.; Houston, R.S.; Flurkey, A.J.; Coolidge, C.M.; Kratochvil, A.L.; Sever, C.K.

    1981-02-01

    A series of uranium-, thorium-, and gold-bearing conglomerates in Late Archean and Early Proterozoic metasedimentary rocks have been discovered in southern Wyoming. The mineral deposits were found by applying the time and strata bound model for the origin of uranium-bearing quartz-pebble conglomerates to favorable rock types within a geologic terrane known from prior regional mapping. No mineral deposits have been discovered that are of current (1981) economic interest, but preliminary resource estimates indicate that over 3418 tons of uranium and over 1996 tons of thorium are present in the Medicine Bow Mountains and that over 440 tons of uranium and 6350 tons of thorium are present in Sierra Madre. Sampling has been inadequate to determine gold resources. High grade uranium deposits have not been detected by work to date but local beds of uranium-bearing conglomerate contain as much as 1380 ppM uranium over a thickness of 0.65 meters. This project has involved geologic mapping at scales from 1/6000 to 1/50,000 detailed sampling, and the evaluation of 48 diamond drill holes, but the area is too large to fully establish the economic potential with the present information. This first volume summarizes the geologic setting and geologic and geochemical characteristics of the uranium-bearing conglomerates. Volume 2 contains supporting geochemical data, lithologic logs from 48 drill holes in Precambrian rocks, and drill site geologic maps and cross-sections from most of the holes. Volume 3 is a geostatistical resource estimate of uranium and thorium in quartz-pebble conglomerates.

  18. Analysis of burnup of Angra 2 PWR nuclear with addition of thorium dioxide fuel using ORIGEN-ARP

    Energy Technology Data Exchange (ETDEWEB)

    Goncalves, Isadora C.; Wichrowski, Caio C.; Oliveira, Claudio L. de; Vellozo, Sergio O.; Baptista, Camila O., E-mail: isadora.goncalves@ime.eb.br, E-mail: wichrowski@ime.eb.br, E-mail: d7luiz@yahoo.com.br, E-mail: vellozo@ime.eb.br, E-mail: camila.oliv.baptista@gmail.com [Instituto Militar de Engenharia (IME), Rio de Janeiro, RJ (Brazil). Secao de Engenharia Nuclear

    2017-11-01

    It is known that isotope {sup 232}thorium is a fertile nuclide with the ability to convert into {sup 233}uranium, a potentially fissile isotope, after absorbing a neutron. As there is a large stock of available thorium in the world, this element shows great promise in mitigate the world energy crisis, more particularly in the problem of uranium scarcity, besides being an alternative nuclear fuel for those currently used in reactors, and yet presenting advantages as an option for the non-proliferation movement, among others. In this study, the analysis of the remaining nuclides of burnup was carried out for the core configuration of a PWR (pressurized water reactor) reactor, specifically the Angra 2 reactor, using only uranium dioxide, its current configuration, and in different configurations including a mixed oxide of uranium and thorium in three concentrations, allowing a preliminary assessment of the feasibility of the modification of the fuel, the resulting production of {sup 233}uranium, the emergence of {sup 231}protactinium (an isotope that only occurs as a fission product of {sup 232}Th) resulting from burning. The study was carried out using data obtained from FSAR (Final Safety Analysis Report) of Angra 2, using the SCALE 6.1, a modeling and simulation nuclear code, especially its ORIGEN-ARP module, which analyzes the depletion of isotopes presents in a reactor. (author)

  19. Rescuing a Treasure Uranium-233

    Energy Technology Data Exchange (ETDEWEB)

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

    2011-01-01

    Uranium-233 (233U) is a synthetic isotope of uranium formed under reactor conditions during neutron capture by natural thorium (232Th). At high purities, this synthetic isotope serves as a crucial reference for accurately quantifying and characterizing natural uranium isotopes for domestic and international safeguards. Separated 233U is stored in vaults at Oak Ridge National Laboratory. These materials represent a broad spectrum of 233U from the standpoint isotopic purity the purest being crucial for precise analyses in safeguarding uranium. All 233U at ORNL currently is scheduled to be down blended with depleted uranium beginning in 2015. Such down blending will permanently destroy the potential value of pure 233U samples as certified reference material for use in uranium analyses. Furthermore, no replacement 233U stocks are expected to be produced in the future due to a lack of operating production capability and the high cost of returning to operation this currently shut down capability. This paper will describe the efforts to rescue the purest of the 233U materials arguably national treasures from their destruction by down blending.

  20. Thorium-U Recycle Facility (7930)

    Data.gov (United States)

    Federal Laboratory Consortium — The Thorium-U Recycle Facility (7930), along with the Transuranic Processing Facility (7920). comprise the Radiochemical Engineering Development Complex. 7930 is a...

  1. Uranium assessment for the Precambrian pebble conglomerates in southeastern Wyoming

    Energy Technology Data Exchange (ETDEWEB)

    Borgman, L.E.; Sever, C.; Quimby, W.F.; Andrew, M.E.; Karlstrom, K.E.; Houston, R.S.

    1981-03-01

    This volume is a geostatistical resource estimate of uranium and thorium in quartz-pebble conglomerates, and is a companion to Volume 1: The Geology and Uranium Potential to Precambrian Conglomerates in the Medicine Bow Mountains and Sierra Madre of Southeastern Wyoming; and to Volume 2: Drill-Hole Data, Drill-Site Geology, and Geochemical Data from the Study of Precambrian Uraniferous Conglomerates of the Medicine Bow Mountains and the Sierra Madre of Southeastern Wyoming.

  2. Depletion Analysis of Modular High Temperature Gas-cooled Reactor Loaded with LEU/Thorium Fuel

    Energy Technology Data Exchange (ETDEWEB)

    Sonat Sen; Gilles Youinou

    2013-02-01

    Thorium based fuel has been considered as an option to uranium-based fuel, based on considerations of resource utilization (Thorium is more widely available when compared to Uranium). The fertile isotope of Thorium (Th-232) can be converted to fissile isotope U-233 by neutron capture during the operation of a suitable nuclear reactor such as High Temperature Gas-cooled Reactor (HTGR). However, the fertile Thorium needs a fissile supporter to start and maintain the conversion process such as U-235 or Pu-239. This report presents the results of a study that analyzed the thorium utilization in a prismatic HTGR, namely Modular High Temperature Gas-Cooled Reactor (MHTGR) that was designed by General Atomics (GA). The collected for the modeling of this design come from Chapter 4 of MHTGR Preliminary Safety Information Document that GA sent to Department of Energy (DOE) on 1995. Both full core and unit cell models were used to perform this analysis using SCALE 6.1 and Serpent 1.1.18. Because of the long mean free paths (and migration lengths) of neutrons in HTRs, using a unit cell to represent a whole core can be non-trivial. The sizes of these cells were set to match the spectral index between unit cell and full core domains. It was found that for the purposes of this study an adjusted unit cell model is adequate. Discharge isotopics and one-group cross-sections were delivered to the transmutation analysis team. This report provides documentation for these calculations

  3. Fabrication of thorium nitrate at the factory at the Bouchet; Fabrication du nitrate de thorium pur a l'usine du Bouchet

    Energy Technology Data Exchange (ETDEWEB)

    Braun, C.; Lorrain, Ch.; Mahut, R.; Mariette, R.; Muller, J.; Prugnard, J. [Commissariat a l' Energie Atomique, Usine du Bouchet, Saclay (France). Centre d' Etudes Nucleaires

    1958-07-01

    A urano-thorianite mineral from Madagascar is industrially treated at the factory of the Bouchet in order to obtain pure thorium in the form of the nitrate and a uranium concentrate in the form of uranate. The required factory was designed and constructed in 1955 and 1956 by the firm Potasse et Engrais Chimiques (P.E.C.) on behalf of the French Atomic Energy authority. The mineral which has previously undergone a gravimetric sorting and enrichment at the mine, is in the form of a heavy rock (the density can be as high as 10), having a cubic structure. It consists principally of a mixture of thorium oxide and uranium oxide and contains between 50 and 75 per cent thorium and between 5 and 20 per cent of uranium. On the same sample a high content in either thorium or uranium in general corresponds to a low content in the other of the two metals; this rule is not however always obeyed absolutely. Among other elements present we shall only mention the Pb, Fe, Ce, Ra and other radioactive elements, since their presence influences the treatment of the mineral. We shall first briefly describe the process, which has already been described in previous publications, we consider to be worthy of attention. (author)Fren. [French] Le minerai d'uranothorianite en provenance de Madagascar est traite industriellement a l'Usine du Bouchet en vue de l'obtentionn sel de thorium pur, le nitrate, et d'un concentre d'uranium, un uranate. L'etude et la construction de l'atelier destine a cet effet ont ete realisees en 1955 et 1956 par la Societe Potasse et Engrais chimiques pour le Commissariat a l'Energie atomique. Le minerai, scheide ou enrichi a la mine par voie gravimetrique, se presente comme une roche dense (la densite peut atteindre 10), de structure cubique. Il est constitue essentiellement d'un melange d'oxyde de thorium et d'oxyde d'uranium qui titre 50 a 75 pour cent de Th et 5 a 20 pour cent d'uranium. A une forte

  4. Matrix Infrared Spectroscopic and Computational Investigations of Novel Small Uranium Containing Molecules - Final Technical Report

    Energy Technology Data Exchange (ETDEWEB)

    Andrews, Lester

    2014-10-17

    Direct reactions of f-element uranium, thorium and lanthanide metal atoms were investigated with small molecules. These metal atoms were generated by laser ablation and mixed with the reagent molecules then condensed with noble gases at 4K. The products were analyzed by absorption of infrared light to measure vibrational frequencies which were confirmed by quantum chemical calculations. We have learned more about the reactivity of uranium atoms with common molecules, which will aid in the develolpment of further applications of uranium.

  5. Uranium in alkaline rocks

    Energy Technology Data Exchange (ETDEWEB)

    Murphy, M.; Wollenberg, H.; Strisower, B.; Bowman, H.; Flexser, S.; Carmichael, I.

    1978-04-01

    Geologic and geochemical criteria were developed for the occurrence of economic uranium deposits in alkaline igneous rocks. A literature search, a limited chemical analytical program, and visits to three prominent alkaline-rock localities (Ilimaussaq, Greenland; Pocos de Caldas, Brazil; and Powderhorn, Colorado) were made to establish criteria to determine if a site had some uranium resource potential. From the literature, four alkaline-intrusive occurrences of differing character were identified as type-localities for uranium mineralization, and the important aspects of these localities were described. These characteristics were used to categorize and evaluate U.S. occurrences. The literature search disclosed 69 U.S. sites, encompassing nepheline syenite, alkaline granite, and carbonatite. It was possible to compare two-thirds of these sites to the type localities. A ranking system identified ten of the sites as most likely to have uranium resource potential.

  6. Uranium-throium isotopes and transition metal fluxes in two oriented manganese nodules from the Central Indian Basin: implications for nodule turnover

    Digital Repository Service at National Institute of Oceanography (India)

    Banakar, V.K.

    -76 71 Elsevier Science Publishers B.V., Amsterdam Letter Section Uranium-thorium isotopes and transition metal fluxes in two oriented manganese nodules from the Central Indian Basin: implications for nodule turnover V.K. Banakar National Institute... of Oceanography, Dona Paula, 403 004 Goa, India (Revision accepted May 7, 1990 ) ABSTRACT Banakar, V.K., 1990. Uranium-thorium isotopes and transition metal fluxes in two oriented manganese nodules from the Central Indian Basin: implications for nodule...

  7. Model Matematik Reduksi Thorium dalam Proses Elektrokoagulasi

    Directory of Open Access Journals (Sweden)

    Prayitno

    2017-11-01

    Full Text Available Thorium reduction by electrocoagulation has been conducted on radioactive waste with thorium contaminant grade of 5x10-4Kg/l through a batch system using aluminium electrodes. This study aims to determine a mathematical model of thorium reduction through speed reaction, constante reaction rate and reaction order which are affected by electrocoagulation process parameters like voltage, time, electrode distance, and pH. The research results the optimum voltage condition at 12.5 V at 1 cm electrode spacing, pH 7, and 30 minutes of processing time with 99.6 % efficiency. Prediction on thorium decline rate constante is obtained through mathematic integral method calculation. The research results thorium decline rate is following second order constante with its value at 5x10-3KgL-1min-1.

  8. Determination of thorium and uranium contents in soil samples ...

    Indian Academy of Sciences (India)

    contents, it is simple, inexpensive and non-destructive and it may be applied to a wide variety of samples such as building materials, environmental samples and naturally occurring radioactive materials (NORM) in petroleum fields. Acknowledgement. One of the authors (TAS) would like to express his deep gratitude to Prof.

  9. Uranium-Thorium evolution of extrasolar silicate worlds

    Science.gov (United States)

    Frank, Elizabeth A.; Mojzsis, Stephen J.

    2013-04-01

    As the suite of known exoplanets expands with the discovery of thousands of worlds around other stars, the need arises to further constrain the range of possible compositions of these objects. This is of particular importance for geophysical modeling of terrestrial exoplanets that may be capable of supporting life. A poorly constrained parameter in these models is radiogenic heating from the long-lived, heat-producing isotopes that are key to keeping planetary interiors warm. In Earth's mantle, the decay of 40K, 232Th, 235U, and 238U provides the majority of the heat output that helps sustain plate tectonics. Given that plate tectonics plays an integral role in keeping Earth's surface habitable, radiogenic heat production is an important factor to consider in modeling terrestrial exoplanets. In published models, radiogenic heat production is scaled from Earth's or chondritic values. Given that Earth's own heat production has decreased at least fivefold over solar system history, it is unreasonable to assume that exoplanets with different ages and geochemical histories should have comparable values. Age is an important factor for heating in that not only will old stars form with a lower metallicity than young stars, but their isotopes will have had a longer period of time to decay. Here we present a model in which we make predictions for the heat generated by 232Th, 235U, and 238U in a solar system within the (galactic) solar cylinder as a function of age. The primary constraints in our model are (i) the ages of our solar system and galaxy, (ii) production ratios of the isotopes, (iii) concentrations of 232Th, 235U, and 238U at the time our solar system formed, and (iv) half-lives. We assumed a hybrid model of the production of these nuclides in our galaxy by taking into account both the burst of nuclides created by massive stars at galaxy formation and those generated in supernovae over galactic history. We numerically solved for the relative contributions of nuclides generated by each process and then used the resulting proportions to constrain the heat they generate in a solar system given its age. Sensitivity tests indicate that of the constraints, the 235U/238U and 232Th/238U production ratios have the most significant effect on the results. By comparison, our predictions are relatively insensitive to the age of the galaxy. The 235U/238U production ratio is particularly fickle due to the relatively short half-life of 235U compared to 238U. For a galaxy age of 12.5 Gyr, the 235U/238U production ratio can only provide a minimum production ratio, found to be 1.42, whereas the allowable spectrum of the 232Th/238U production ratio is found to be 1.02 to 1.64, the higher values of which are consistent with published ratios. To ground-truth our model, we compared predicted Th/U ratios to published observations of ancient, metal-poor halo stars. Despite the wide error bars for the calculated ages of these stars due to observational limitations, our model predicts Th/U ratios consistent with observations. As such, in addition to making predictions for heat production in extrasolar systems, our model may also be used to constrain stellar ages.

  10. Uranium and thorium in fossil bones : activity ratios and dating

    NARCIS (Netherlands)

    Plicht, J. van der; Bartstra, G.J.

    1989-01-01

    We have analysed fossil bones by U-series disequilibrium from five different sites (Ngandong and Sonde, Indonesia; Gold Ox Hill, People's Republic of China; Pestera, Romania and Ksar Akil, Lebanon). Two samples were taken from all bones: one representing surface material, and one from the inner bone

  11. Determination of thorium and uranium contents in soil samples ...

    Indian Academy of Sciences (India)

    Experimental Nuclear Physics Department, Atomic Energy Authority, Nuclear Research Center, Abu Zabaal, 13759 Cairo, Egyp; Experimental Nuclear Physics Department, Atomic Energy Authority, Nuclear Research Center, Abu Zabaal, 13759 Cairo, Egypt; Faculty of Girls for Art, Science and Education, Ain-Shams ...

  12. OPTIMIZATION OF HETEROGENEOUS UTILIZATION OF THORIUM IN PWRS TO ENHANCE PROLIFERATION RESISTANCE AND REDUCE WASTE.

    Energy Technology Data Exchange (ETDEWEB)

    TODOSOW,M.; KAZIMI,M.

    2004-08-01

    Issues affecting the implementation, public perception and acceptance of nuclear power include: proliferation, radioactive waste, safety, and economics. The thorium cycle directly addresses the proliferation and waste issues, but optimization studies of core design and fuel management are needed to ensure that it fits within acceptable safety and economic margins. Typical pressurized water reactors, although loaded with uranium fuel, produce 225 to 275 kg of plutonium per gigawatt-year of operation. Although the spent fuel is highly radioactive, it nevertheless offers a potential proliferation pathway because the plutonium is relatively easy to separate, amounts to many critical masses, and does not present any significant intrinsic barrier to weapon assembly. Uranium 233, on the other hand, produced by the irradiation of thorium, although it too can be used in weapons, may be ''denatured'' by the addition of natural, depleted or low enriched uranium. Furthermore, it appears that the chemical behavior of thoria or thoria-urania fuel makes it a more stable medium for the geological disposal of the spent fuel. It is therefore particularly well suited for a once-through fuel cycle. The use of thorium as a fertile material in nuclear fuel has been of interest since the dawn of nuclear power technology due to its abundance and to potential neutronic advantages. Early projects include homogeneous mixtures of thorium and uranium oxides in the BORAX-IV, Indian Point I, and Elk River reactors, as well as heterogeneous mixtures in the Shippingport seed-blanket reactor. However these projects were developed under considerably different circumstances than those which prevail at present. The earlier applications preceded the current proscription, for non-proliferation purposes, of the use of uranium enriched to more than 20 w/o in {sup 235}U, and has in practice generally prohibited the use of uranium highly enriched in {sup 235}U. They were designed when

  13. Facile and Efficient Decontamination of Thorium from Rare Earths Based on Selective Selenite Crystallization.

    Science.gov (United States)

    Wang, Yaxing; Lu, Huangjie; Dai, Xing; Duan, Tao; Bai, Xiaojing; Cai, Yawen; Yin, Xuemiao; Chen, Lanhua; Diwu, Juan; Du, Shiyu; Zhou, Ruhong; Chai, Zhifang; Albrecht-Schmitt, Thomas E; Liu, Ning; Wang, Shuao

    2018-02-19

    The coexistence of radioactive contaminants (e.g., thorium, uranium, and their daughters) in rare earth minerals introduces significant environmental, economic, and technological hurdles in modern rare earth production. Efficient, low cost, and green decontamination strategies are therefore desired to ameliorate this problem. We report here a single-step and quantitative decontamination strategy of thorium from rare earths based on a unique periodic trend in the formation of crystalline selenite compounds across the lanthanide series, where Ce(III) is fully oxidized in situ to Ce(IV). This gives rise to a crystallization system that is highly selective to trap tetravalent f-blocks while all other trivalent lanthanides completely remain in solution when coexist. These results are bolstered by first-principles calculations of lattice energies and an examination of bonding in these compounds. This system is contrasted with typical natural and synthetic systems, where trivalent and tetravalent f-block elements often cocrystallize. The separation factors after one round of crystallization were determined from binary systems of Th(IV)/La(III), Th(IV)/Eu(III), and Th(IV)/Yb(III) to reach 2.1 × 10 5 , 1.2 × 10 5 , and 9 × 10 4 , respectively. Selective crystallization of thorium from a simulated monazite composite yields a separation factor of 1.9 × 10 3 with nearly quantitative removal of thorium.

  14. Antineutrino monitoring of thorium reactors

    Science.gov (United States)

    Akindele, Oluwatomi A.; Bernstein, Adam; Norman, Eric B.

    2016-09-01

    Various groups have demonstrated that antineutrino monitoring can be successful in assessing the plutonium content in water-cooled nuclear reactors for nonproliferation applications. New reactor designs and concepts incorporate nontraditional fuel types and chemistry. Understanding how these properties affect the antineutrino emission from a reactor can extend the applicability of antineutrino monitoring. Thorium molten salt reactors breed 233U, that if diverted constitute a direct use material as defined by the International Atomic Energy Agency (IAEA). The antineutrino spectrum from the fission of 233U has been estimated for the first time, and the feasibility of detecting the diversion of 8 kg of 233U, within a 30 day timeliness goal has been evaluated. The antineutrino emission from a thorium reactor operating under normal conditions is compared to a diversion scenario by evaluating the daily antineutrino count rate and the energy spectrum of the detected antineutrinos at a 25 m standoff. It was found that the diversion of a significant quantity of 233U could not be detected within the current IAEA timeliness detection goal using either tests. A rate-time based analysis exceeded the timeliness goal by 23 days, while a spectral based analysis exceeds this goal by 31 days.

  15. Thorium isotopes in human tissues

    Energy Technology Data Exchange (ETDEWEB)

    Stehney, A.F.; Lucas, H.F.

    1991-12-31

    Concentrations of {sup 232}Th and activity ratios of {sup 228}Th to {sup 232}Th and {sup 230}Th to {sup 232}Th were determined in autopsy samples from five former employees of a thorium refinery. The ranges of {sup 232}Th activity concentrations (mBq g{sup {minus}1}) were 0.17--94 in lungs, 3.9--1210 in pulmonary lymph nodes, 0.14--1.19 in bones, 0.015--0.68 in liver, 0.97--5.8 in spleen, and 0.009--0.068 in kidneys. These concentrations are 10 to 1000 times greater than have been reported for persons not occupationally exposed to Th. In most of the samples, the ratios of {sup 230}Th to {sup 232}Th and {sup 228}Th to {sup 232}Th activity at death of the subject were 0.1--0.2 and 0.2--0.4, respectively. Thorium-228 to {sup 228}Ra activity ratios ({plus_minus} standard errors) of 0.86 {plus_minus} 0.11 in lungs and 1.18 {plus_minus} 0.13 in lymph nodes of one subject were obtained by calculation from ratios of {sup 228}Th to {sup 232}Th.

  16. Extraction of some strategic elements from thorium–uranium concentrate using bioproducts of Aspergillus ficuum and Pseudomonas aeruginosa

    OpenAIRE

    Osman A. Desouky; El-Mougith, Abdou A.; Wesam A. Hassanien; Gamal S. Awadalla; Shimaa S. Hussien

    2016-01-01

    The activity of the bioproducts from Aspergillus ficuum and Pseudomonas aeruginosa for extraction of thorium (Th4+), uranium (UO22+) and rare earth elements (REEs) from thorium–uranium concentrate was studied. P. aeruginosa produce element-specific ligand (siderophore) that is able to change pH and enhance chelation of Th4+ and UO22+. The produced siderophore at pH 5.3 has the ability to bioleach and is complexed with 68.00% of uranium and 65.00% of thorium. Also, A. ficuum produced different...

  17. High-quality thorium TRISO fuel performance in HTGRs

    Energy Technology Data Exchange (ETDEWEB)

    Verfondern, Karl [Forschungszentrum Juelich GmbH (Germany); Allelein, Hans-Josef [Forschungszentrum Juelich GmbH (Germany); Technische Hochschule Aachen (Germany); Nabielek, Heinz; Kania, Michael J.

    2013-11-01

    Thorium as a nuclear fuel has received renewed interest, because of its widespread availability and the good irradiation performance of Th and mixed (Th,U) oxide compounds as fuels in nuclear power systems. Early HTGR development employed thorium together with high-enriched uranium (HEU). After 1980, HTGR fuel systems switched to low-enriched uranium (LEU). After completing fuel development for the AVR and the THTR with BISO coated particles, the German program expanded its efforts utilizing thorium and HEU TRISO coated particles in advanced HTGR concepts for process heat applications (PNP) and direct-cycle electricity production (HHT). The combination of a low-temperature isotropic (LTI) inner and outer pyrocarbon layers surrounding a strong, stable SiC layer greatly improved manufacturing conditions and the subsequent contamination and defective particle fractions in production fuel elements. In addition, this combination provided improved mechanical strength and a higher degree of solid fission product retention, not known previously with high-temperature isotropic (HTI) BISO coatings. The improved performance of the HEU (Th, U)O{sub 2} TRISO fuel system was successfully demonstrated in three primary areas of development: manufacturing, irradiation testing under normal operating conditions, and accident simulation testing. In terms of demonstrating performance for advanced HTGR applications, the experimental failure statistic from manufacture and irradiation testing are significantly below the coated particle requirements specified for PNP and HHT designs at the time. Covering a range to 1300 C in normal operations and 1600 C in accidents, with burnups to 13% FIMA and fast fluences to 8 x 10{sup 25} n/m{sup 2} (E> 16 fJ), the performance results exceed the design limits on manufacturing and operational requirements for the German HTR-Modul concept, which are 6.5 x 10{sup -5} for manufacturing, 2 x 10{sup -4} for normal operating conditions, and 5 x 10{sup -4

  18. Concomitant carboxylate and oxalate formation from the activation of CO{sub 2} by a thorium(III) complex

    Energy Technology Data Exchange (ETDEWEB)

    Formanuik, Alasdair; Ortu, Fabrizio; Mills, David P. [School of Chemistry, The University of Manchester (United Kingdom); Inman, Christopher J. [Department of Chemistry and Biochemistry, School of Life Sciences, University of Sussex, Brighton (United Kingdom); Kerridge, Andrew [Department of Chemistry, Lancaster University (United Kingdom); Castro, Ludovic; Maron, Laurent [LPCNO, CNRA et INSA, Universite Paul Sabatier, Toulouse (France)

    2016-12-12

    Improving our comprehension of diverse CO{sub 2} activation pathways is of vital importance for the widespread future utilization of this abundant greenhouse gas. CO{sub 2} activation by uranium(III) complexes is now relatively well understood, with oxo/carbonate formation predominating as CO{sub 2} is readily reduced to CO, but isolated thorium(III) CO{sub 2} activation is unprecedented. We show that the thorium(III) complex, [Th(Cp''){sub 3}] (1, Cp''={C_5H_3(SiMe_3)_2-1,3}), reacts with CO{sub 2} to give the mixed oxalate-carboxylate thorium(IV) complex [{Th(Cp'')_2[κ"2-O_2C{C_5H_3-3,3'-(SiMe_3)_2}]}{sub 2}(μ-κ{sup 2}:κ{sup 2}-C{sub 2}O{sub 4})] (3). The concomitant formation of oxalate and carboxylate is unique for CO{sub 2} activation, as in previous examples either reduction or insertion is favored to yield a single product. Therefore, thorium(III) CO{sub 2} activation can differ from better understood uranium(III) chemistry. (copyright 2016 The Authors. Published by Wiley-VCH Verlag GmbH and Co. KGaA.)

  19. Uranium;L'uranium

    Energy Technology Data Exchange (ETDEWEB)

    Poty, B. [CNRS, 54 - Gondreville (France); Cuney, M.; Bruneton, P.; Virlogeux, D.; Capus, G.

    2010-03-15

    With the worldwide revival of nuclear energy comes the question of uranium reserves. For more than 20 years, nuclear energy has been neglected and uranium prospecting has been practically abandoned. Therefore, present day production covers only 70% of needs and stocks are decreasing. Production is to double by 2030 which represents a huge industrial challenge. The FBR-type reactors technology, which allows to consume the whole uranium content of the fuel, is developing in several countries and will ensure the long-term development of nuclear fission. However, the implementation of these reactors (the generation 4) will be progressive during the second half of the 21. century. For this reason an active search for uranium ores will be necessary during the whole 21. century to ensure the fueling of light water reactors which are huge uranium consumers. This dossier covers all the aspects of natural uranium production: mineralogy, geochemistry, types of deposits, world distribution of deposits with a particular attention given to French deposits, the exploitation of which is abandoned today. Finally, exploitation, ore processing and the economical aspects are presented. Contents: 1 - the uranium element and its minerals: from uranium discovery to its industrial utilization, the main uranium minerals (minerals with tetravalent uranium, minerals with hexavalent uranium); 2 - uranium in the Earth's crust and its geochemical properties: distribution (in sedimentary rocks, in magmatic rocks, in metamorphic rocks, in soils and vegetation), geochemistry (uranium solubility and valence in magmas, uranium speciation in aqueous solution, solubility of the main uranium minerals in aqueous solution, uranium mobilization and precipitation); 3 - geology of the main types of uranium deposits: economical criteria for a deposit, structural diversity of deposits, classification, world distribution of deposits, distribution of deposits with time, superficial deposits, uranium

  20. Economics and utilization of thorium in nuclear reactors. Technical annexes 1 and 2

    Energy Technology Data Exchange (ETDEWEB)

    1978-05-01

    An assessment of the impact of utilizing the /sup 233/U/thorium fuel cycle in the U.S. nuclear economy is strongly dependent upon several decisions involving nuclear energy policy. These decisions include: (1) to recycle or not recycle fissile material; (2) if fissile material is recycled, to recycle plutonium, /sup 233/U, or both; and (3) to deploy or not to deploy advanced reactor designs such as Fast Breeder Reactors (FBR's), High Temperature Gas Reactors (HTGR's), and Canadian Deuterium Uranium Reactors (CANDU's). This report examines the role of thorium in the context of the above policy decisions while focusing special attention on economics and resource utilization.

  1. A Review of Thorium Utilization as an option for Advanced Fuel Cycle--Potential Option for Brazil in the Future

    Energy Technology Data Exchange (ETDEWEB)

    Maiorino, J.R.; Carluccio, T.

    2004-10-03

    Since the beginning of Nuclear Energy Development, Thorium was considered as a potential fuel, mainly due to the potential to produce fissile uranium 233. Several Th/U fuel cycles, using thermal and fast reactors were proposed, such as the Radkwoski once through fuel cycle for PWR and VVER, the thorium fuel cycles for CANDU Reactors, the utilization in Molten Salt Reactors, the utilization of thorium in thermal (AHWR), and fast reactors (FBTR) in India, and more recently in innovative reactors, mainly Accelerator Driven System, in a double strata fuel cycle. All these concepts besides the increase in natural nuclear resources are justified by non proliferation issues (plutonium constrain) and the waste radiological toxicity reduction. The paper intended to summarize these developments, with an emphasis in the Th/U double strata fuel cycle using ADS. Brazil has one of the biggest natural reserves of thorium, estimated in 1.2 millions of tons of ThO{sub 2}, as will be reviewed in this paper, and therefore R&D programs would be of strategically national interest. In fact, in the past there was some projects to utilize Thorium in Reactors, as the ''Instinto/Toruna'' Project, in cooperation with France, to utilize Thorium in Pressurized Heavy Water Reactor, in the mid of sixties to mid of seventies, and the thorium utilization in PWR, in cooperation with German, from 1979-1988. The paper will review these initiatives in Brazil, and will propose to continue in Brazil activities related with Th/U fuel cycle.

  2. Rocks of the Thirtynine Mile volcanic field as possible sources of uranium for epigenetic deposits in central Colorado, USA.

    Science.gov (United States)

    Dickinson, K.A.

    1987-01-01

    The most likely volcanic source rock for uranium in epigenetic deposits of the Tallahassee Creek uranium district and nearby areas is the Wall Mountain Tuff. The widespread occurrence of the Tuff, its high apparent original uranium content, approx 11 ppm, and its apparent loss of uranium from devitrification and other alteration suggest its role in providing that element. An estimate of the original Th/U ratio is based on the present thorium and uranium contents of the basal vitrophyre of the Tuff from Castle Rock Gulch, Hecla Junction and other areas.-from Author

  3. Burn-up calculation of different thorium-based fuel matrixes in a thermal research reactor using MCNPX 2.6 code

    Directory of Open Access Journals (Sweden)

    Gholamzadeh Zohreh

    2014-12-01

    Full Text Available Decrease of the economically accessible uranium resources and the inherent proliferation resistance of thorium fuel motivate its application in nuclear power systems. Estimation of the nuclear reactor’s neutronic parameters during different operational situations is of key importance for the safe operation of nuclear reactors. In the present research, thorium oxide fuel burn-up calculations for a demonstrative model of a heavy water- -cooled reactor have been performed using MCNPX 2.6 code. Neutronic parameters for three different thorium fuel matrices loaded separately in the modelled thermal core have been investigated. 233U, 235U and 239Pu isotopes have been used as fissile element in the thorium oxide fuel, separately. Burn-up of three different fuels has been calculated at 1 MW constant power. 135X and 149Sm concentration variations have been studied in the modelled core during 165 days burn-up. Burn-up of thorium oxide enriched with 233U resulted in the least 149Sm and 135Xe productions and net fissile production of 233U after 165 days. The negative fuel, coolant and void reactivity of the used fuel assures safe operation of the modelled thermal core containing (233U-Th O2 matrix. Furthermore, utilisation of thorium breeder fuel demonstrates several advantages, such as good neutronic economy, 233U production and less production of long-lived α emitter high radiotoxic wastes in biological internal exposure point of view

  4. Analysis of the effects of stirring condition of separation of thorium in the elution process of monazite partial solution by solvent impregnated resin method

    Science.gov (United States)

    Prassanti, R.; Putra, D. S.; Kusuma, B. P.; Nawawi, F. W.

    2018-01-01

    Monazite is a natural mineral which contains abundant valuable element such as Radioactive Element and Rare Earth Element(REE). In this experiment, it is proven that solution of residual Thorium Sulfate from Monazite mineral process, can be seperated selectively by using extracting method of Solvent Impregnated Resin(SIR), with the elutant solution HNO3. In the earlier process, Thorium solution is conditioned at PH 1 by using H2SO4. Then REE, Thorium and Uranium elements are seperated. This seperation is conducted by using adsorption method by Amberlite XAD-16 Resin, which has been impregnated by Tributhyl Phosphate extractant. It is continued with elution process, which is aimed to obtain Thorium solution of a higher level of concentration. This elution process is conducted by using HNO3, with the elution variables of the lenght of mixing and amount concentration elutant. Based on this experiment, SIR extracting method is able to dissolve Thorium solution until 63,2%grade and a higher level of %grade about 92,40%. It can be concluded that this SIR method can extracted Thorium elements selectively, improve extracting process recovery, and determine optimum stripping condition in the 45th minutes with elutant concentration of 1,0M HNO3.

  5. Vil løyse global energikrise med thorium

    CERN Multimedia

    Aure, Gyri

    2007-01-01

    A professor from Bergen claims thorium can contribute to save the world from a global energy crisis. He wants Norway to construct the first accelerator driven reactor in the world powered by thorium. (5 pages)

  6. Occupational exposures to thorium in two Brazilian niobium plants

    Energy Technology Data Exchange (ETDEWEB)

    Dias da Cunha, K.; Lipsztein, J.L.; Barros Leite, C.V

    1998-07-01

    The worker exposure to thorium-bearing airborne particulate was estimated in two Brazilian plants that process niobium minerals, one in the Amazon Forest (Plant A) and the other in the State of Goias (Plant B). The aerosol particle size and the thorium concentrations in the respirable fractions of aerosol concentrations were determined. Results indicate that in Plant A, the MMAD (Mass Median Aerodynamic Diameter) of particles containing thorium were in the range 1.1 to 1.8 {mu}m: in Plant B they were in the range 1.1 to 3.4 {mu}m. The thorium faeces concentrations before the vacation were higher than thorium faeces concentrations in the control group. After the vacation the thorium faeces concentrations were similar to the thorium faeces concentrations in the control group. These results indicate that the thorium incorporation by the workers are mostly due to ingestion. (author)

  7. Synthesis of uranyl acetylacetonate free of thorium 234

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Rendon, R.; Solache R, M.; Tenorio, D. (Instituto Nacional de Investigaciones Nucleares, Mexico City)

    1983-01-01

    A technique is described for synthesizing uranyl acetylacetonate free of thorium-234, and the method utilized in identifying it. The aim in the preparation of the thorium-234 free compound was to study the chemical effects produced by U-238 decay by means of detection only of the thorium-234 decay product.

  8. Measurements of /sup 234/U, /sup 238/U and /sup 230/Th in excreta of uranium-mill crushermen

    Energy Technology Data Exchange (ETDEWEB)

    Fisher, D.R.; Jackson, P.O.; Brodacynski, G.G.; Scherpelz, R.I.

    1982-07-01

    Uranium and thorium levels in excreta of uranium mill crushermen who are routinely exposed to airborne uranium ore dust were measured. The purpose was to determine whether /sup 230/Th was preferentially retained over either /sup 234/U or /sup 238/U in the body. Urine and fecal samples were obtained from fourteen active crushermen with long histories of exposure to uranium ore dust, plus four retired crushermen and three control individuals for comparison. Radiochemical procedures were used to separate out the uranium and thorium fractions, which were then electroplated on stainless steel discs and assayed by alpha spectrometry. Significantly greater activity levels of /sup 234/U and /sup 238/U were measured in both urine and fecal samples obtained from uranium mill crushermen, indicating that uranium in the inhaled ore dust was cleared from the body with a shorter biological half-time than the daughter product /sup 230/Th. The measurements also indicated that uranium and thorium separate in vivo and have distinctly different metabolic pathways and transfer rates in the body. The appropriateness of current ICRP retention and clearance parameters for /sup 230/Th in ore dust is questioned.

  9. Optimization of the self-sufficient thorium fuel cycle for CANDU power reactors

    Directory of Open Access Journals (Sweden)

    Bergelson Boris R.

    2008-01-01

    Full Text Available The results of optimization calculations for CANDU reactors operating in the thorium cycle are presented in this paper. Calculations were performed to validate the feasibility of operating a heavy-water thermal neutron power reactor in a self-sufficient thorium cycle. Two modes of operation were considered in the paper: the mode of preliminary accumulation of 233U in the reactor itself and the mode of operation in a self-sufficient cycle. For the mode of accumulation of 233U, it was assumed that enriched uranium or plutonium was used as additional fissile material to provide neutrons for 233U production. In the self-sufficient mode of operation, the mass and isotopic composition of heavy nuclei unloaded from the reactor should provide (after the removal of fission products the value of the multiplication factor of the cell in the following cycle K>1. Additionally, the task was to determine the geometry and composition of the cell for an acceptable burn up of 233U. The results obtained demonstrate that the realization of a self-sufficient thorium mode for a CANDU reactor is possible without using new technologies. The main features of the reactor ensuring a self-sufficient mode of operation are a good neutron balance and moving of fuel through the active core.

  10. Effect of Using Thorium Molten Salts on the Neutronic Performance of PACER

    Science.gov (United States)

    Acır, Adem; Übeyli, Mustafa

    2010-04-01

    Utilization of nuclear explosives can produce a significant amount of energy which can be converted into electricity via a nuclear fusion power plant. An important fusion reactor concept using peaceful nuclear explosives is called as PACER which has an underground containment vessel to handle the nuclear explosives safely. In this reactor, Flibe has been considered as a working coolant for both tritium breeding and heat transferring. However, the rich neutron source supplied from the peaceful nuclear explosives can be used also for fissile fuel production. In this study, the effect of using thorium molten salts on the neutronic performance of the PACER was investigated. The computations were performed for various coolants bearing thorium and/or uranium-233 with respect to the molten salt zone thickness in the blanket. Results pointed out that an increase in the fissile content of the salt increased the neutronic performance of the reactor remarkably. In addition, higher energy production was obtained with thorium molten salts compared to the pure mode of the reactor. Moreover, a large quantity of 233U was produced in the blanket in all cases.

  11. Borehole Logging for Uranium by Gamma-Ray Spectrometry

    DEFF Research Database (Denmark)

    Løvborg, Leif; Nyegaard, P.; Christiansen, E. M.

    1980-01-01

    The resources in a large syngenetic deposit of low-grade uranium (U) ore with thorium at Kvanefjeld, South Greenland, were evaluated by spectrometric gamma-ray logging of 23 boreholes, 46 mm in diameter and 200 m deep. The borehole probe's detector contained 22 cm3 of sodium-iodide, and the photo......The resources in a large syngenetic deposit of low-grade uranium (U) ore with thorium at Kvanefjeld, South Greenland, were evaluated by spectrometric gamma-ray logging of 23 boreholes, 46 mm in diameter and 200 m deep. The borehole probe's detector contained 22 cm3 of sodium...... to another; this variation is believed to be caused by emanation of radon (Rn) from the borehole walls. Block calculations based on individual calibration constants for the boreholes logged made it possible to obtain a reliable estimate of the tonnage of U. This estimate was only slightly different from...

  12. Large-Scale Physical Separation of Depleted Uranium from Soil

    Science.gov (United States)

    2012-09-01

    the garden versus approximately 18 months in the Catch Box); differences in soil chemistry (the DU garden was a desert soil, the Catch Box...increased tendency to burn after prolonged exposure to moist air. A few metals, such as thorium, uranium, and plutonium , emit ionizing radiation that...Catch Box), differences in soil chemistry (the DU garden was a desert soil, the Catch Box construction grade sand), and/or better aqueous drainage in

  13. The low enriched fuel cycle in the GA 1160 MW design and the switch-over to thorium

    Energy Technology Data Exchange (ETDEWEB)

    Larsen, H.

    1974-03-15

    Calculations for the GA 1160 MW HTR are presented. The aim of these investigations was to compare the Low Enriched Uranium (LEU) cycle and the Thorium cycle for the GA 1160 MW HTR both using the same GA designed integral block fuel element. The total fuel cycle cost for the equilibrium cycle comes out to be about 16% cheaper for the Thorium cycle than for the Low-Enriched cycle. However, these favorable results for the thorium cycle are completely dependent on the availability of reprocessing and refabrication facilities, for costs comparable with the costs used for these investigations. The possibility of starting the reactor on a LEU 3 year cycle and later switching over to a thorium 4 year cycle was investigated. No cost penalties were found to be paid during the switch-over. The problems of local power peaks and age factors were not investigated in greater detail as only integral physical quantities were obtained from the neutron physics calculations. However, no indications of any problem in the switch-over phase were given. Elaborate 3-dimensional methods are necessary for further investigation of these types of problems.

  14. 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)

  15. Geochemical behaviour of uranium and thorium in the waste of a uranium conversion facility

    OpenAIRE

    Fernandes, Teresa

    2017-01-01

    Los residuos contenidos en las balsas de decantación de la planta de conversión de uranio de Comurhex - Malvési, Francia, han sido caracterizados con el objectivo de investigar el comportamiento de uranio y torio en este entorno específico. El residuo es una sucesión de estratos heterogénea que comprende una mezcla de los efluentes del proceso con el suelo (que han tenido su origen en la re-construcción de los diques de las balsas, el efluente de lodo, y los antiguos desechos d...

  16. Nuclear fission and diplomacy. Kernsplijting en diplomatie; De Nederlandse politiek ten aanzien van de vreedzame toepassing van kernenergie, 1939-1957

    Energy Technology Data Exchange (ETDEWEB)

    Van Splunter, J.M. (Vakgroep Internationale Betrekkingen en Volkenrecht, Faculteit PSCW, Univ. van Amsterdam (Netherlands))

    1993-01-01

    The title study, based on archive investigations in the Netherlands, the United States and Great Britain, deals with early phase of Dutch involvement in nuclear energy, that is up to the signing of the Euratom treaty in 1957. It concentrates upon the international aspects of Dutch activities in nuclear energy, especially upon relations with other countries active in the field. In chapter two the Dutch government policy regarding the strategic materials uranium and thorium is discussed. Attention is paid to the interest of the United States for such materials. It is explained why the Dutch government kept it a secret that they possessed a certain amount of uranium and why they negotiated the thorium reserves which were mined in the Netherlands East Indies (now Indonesia). In chapter three the Dutch policy in the United Nations regarding the so-called Baruch plan, being the USA-proposal for international control and management of the use of nuclear energy, and the counter proposal of the USSR, the Gromyko plan, in the period 1946-152 is outlined. In chapter four an overview is given of how the Dutch nuclear energy research in the first ten years after the Second World War was set up and organized. As a result of US president Eisenhower's 'Atoms for Peace' speech, held in December 1953, the Americans offered to cooperate with Western European countries, already involved in research on peaceful applications of nuclear energy. This change in the US-policy of secrecy is described in chapter five. The consequences of that speech are dealt with in chapter six. It resulted, amongst other things in the foundation of the Reactor Centre Netherlands (RCN), now Netherlands Energy Research Foundation (ECN). It is concluded that only in the last years of the period, studied in this thesis, the Netherlands reconciled itself to American supremacy, partly explained by the weakly developed political structure in the Netherlands regarding the nuclear energy policy. 17

  17. On the role of fusion neutron source with thorium blanket in forming the nuclide composition of the nuclear fuel cycle of the Russian Federation

    Energy Technology Data Exchange (ETDEWEB)

    Shmelev, A. N.; Kulikov, G. G., E-mail: ggkulikov@mephi.ru [National Research Nuclear University (Moscow Engineering Physics Institute) (Russian Federation)

    2016-12-15

    The possible role of available thorium resources of the Russian Federation in utilization of thorium in the closed (U–Pu)-fuel cycle of nuclear power is considered. The efficiency of application of fusion neutron sources with thorium blanket for economical use of available thorium resources is demonstrated. The objective of this study is the search for a solution of such major tasks of nuclear power as reduction of the amount of front-end operations in the nuclear fuel cycle and enhancement of its protection against uncontrolled proliferation of fissile materials with the smallest possible alterations in the fuel cycle. The earlier results are analyzed, new information on the amount of thorium resources of the Russian Federation is used, and additional estimates are made. The following basic results obtained on the basis of the assumption of involving fusion reactors with Th-blanket in future nuclear power for generation of the light uranium fraction {sup 232+233+234}U and {sup 231}Pa are formulated. (1) The fuel cycle would shift from fissile {sup 235}U to {sup 233}U, which is more attractive for thermal power reactors. (2) The light uranium fraction is the most “protected” in the uranium fuel component, and being mixed with regenerated uranium, it would become reduced-enrichment uranium fuel, which would relieve the problem of nonproliferation of the fissile material. (3) The addition of {sup 231}Pa into the fuel would stabilize its neutron-multiplying properties, thus making it possible to implement a long fuel residence time and, as a consequence, increase the export potential of the whole nuclear power technology. (4) The available thorium resource in the vicinity of Krasnoufimsk is sufficient for operation of the large-scale nuclear power industry of the Russian Federation with an electric power of 70 GW for more than one quarter of a century. The general conclusion is that involvement of a small number of fusion reactors with Th-blanket in the future

  18. Uranium recovery from waste of the nuclear fuel cycle plants at IPEN-CNEN/SP, Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Freitas, Antonio A.; Ferreira, Joao C.; Zini, Josiane; Scapin, Marcos A.; Carvalho, Fatima Maria Sequeira de, E-mail: afreitas@ipen.b, E-mail: jcferrei@ipen.b, E-mail: jzini@ipen.b, E-mail: mascapin@ipen.b, E-mail: fatimamc@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2011-07-01

    Sodium diuranate (DUS) is a uranium concentrate produced in monazite industry with 80% typical average grade of U{sup 3}O{sup 8}, containing sodium, silicon, phosphorus, thorium and rare earths as main impurities. Purification of such concentrate was achieved at the nuclear fuel cycle pilot plants of uranium at IPEN by nitric dissolution and uranium extraction into an organic phase using TBP/Varsol, while the aqueous phase retains impurities and a small quantity of non extracted uranium; both can be recovered later by precipitation with sodium hydroxide. Then the residual sodium diuranate goes to a long term storage at a safeguards deposit currently reaching 20 tonnes. This work shows how uranium separation and purification from such bulk waste can be achieved by ion exchange chromatography, aiming at decreased volume and cost of storage, minimization of environmental impacts and reduction of occupational doses. Additionally, the resulting purified uranium can be reused in nuclear fuel cycle.(author)

  19. Hybrid fusion–fission reactor with a thorium blanket: Its potential in the fuel cycle of nuclear reactors

    Energy Technology Data Exchange (ETDEWEB)

    Shmelev, A. N., E-mail: shmelan@mail.ru; Kulikov, G. G., E-mail: ggkulikov@mephi.ru; Kurnaev, V. A., E-mail: kurnaev@yandex.ru; Salahutdinov, G. H., E-mail: saip07@mail.ru; Kulikov, E. G., E-mail: egkulikov@mephi.ru; Apse, V. A., E-mail: apseva@mail.ru [National Research Nuclear University MEPhI (Moscow Engineering Physics Institute) (Russian Federation)

    2015-12-15

    Discussions are currently going on as to whether it is suitable to employ thorium in the nuclear fuel cycle. This work demonstrates that the {sup 231}Pa–{sup 232}U–{sup 233}U–Th composition to be produced in the thorium blanket of a hybrid thermonuclear reactor (HTR) as a fuel for light-water reactors opens up the possibility of achieving high, up to 30% of heavy metals (HM), or even ultrahigh fuel burnup. This is because the above fuel composition is able to stabilize its neutron-multiplying properties in the process of high fuel burnup. In addition, it allows the nuclear fuel cycle (NFC) to be better protected against unauthorized proliferation of fissile materials owing to an unprecedentedly large fraction of {sup 232}U (several percent!) in the uranium bred from the Th blanket, which will substantially hamper the use of fissile materials in a closed NFC for purposes other than power production.

  20. Preparation of uranium-based oxide catalysts; Preparation de catalyseurs oxydes a base d'uranium

    Energy Technology Data Exchange (ETDEWEB)

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

    1965-07-01

    We have studied the thermal decomposition of uranyl and uranium IV oxalates as a mean of producing uranium dioxide. We have isolated the main intermediate phases of the decompositions and have indexed the lines of their X-ray diffraction patterns. The oxides produced by the decomposition are ill-defined and unstable: they strongly absorb atmospheric oxygen with modification of the composition and, in certain cases, of the structure (pyrophoric oxide). With a view to obtaining stable oxides, we have prepared mixed uranium-thorium oxalates. In order to prepare an oxalate having a homogeneous composition, it is necessary to adopt a well-defined preparation method: the addition of solutions of thorium and uranium IV nitrates to a continually saturated oxalic acid solution. The mixed oxide obtained from the thermal decomposition of an oxalate U{sub x}Th{sub 1-x}(C{sub 2}O{sub 4}){sub 2}, 2 H{sub 2}O at 500 C for 24 hours in a current of oxygen leads to a cubic structure which is well-defined both in the bulk and superficially when x is less than 0.35. Above this atomic concentration of uranium, some uranium moves out of the lattice in the form of UO{sub 3} or U{sub 3}O{sub 8} according to the temperature. The mixed oxide is not stoichiometric,(U{sub x}Th{sub 1-x}O{sub 2+y}) and the average degree of oxidation of the uranium varies with the temperature and partial oxygen pressure. The oxides thus formed have a high surface area. By dissolving the mixed oxalates in a concentrated solution of ammonium oxalate, it is possible to deposit the catalyst on a support, but the differences in the solubilities of the thorium and uranium IV oxalates in the ammonium oxalate make it impossible to prepare double salts formed either of thorium and uranium and of ammonium. (author) [French] Nous avons etudie la decomposition thermique des oxalates d'uranyle et d'uranium IV en vue d'aboutir au dioxide d'uranium. Nous avons pu isoler les principales phases

  1. Thorium: An energy source for the world of tomorrow ?

    CERN Multimedia

    CERN. Geneva

    2014-01-01

    To meet the tremendous world energy needs, systematic R&D has to be pursued to replace fossil fuels. The ThEC13 conference organized by iThEC at CERN last October has shown that thorium is seriously considered by developing countries as a key element of their energy strategy. Developed countries are also starting to move in the same direction. How thorium could make nuclear energy (based on thorium) acceptable to society will be discussed. Thorium can be used both to produce energy and to destroy nuclear waste. As thorium is not fissile, one elegant option is to use an accelerator, in so-called “Accelerator Driven Systems (ADS)”, as suggested by Carlo Rubbia. CERN’s important contributions to R&D on thorium related issues will be mentioned as well as the main areas where CERN could contribute to this field in the future.

  2. Concentration and purification of plutonium or thorium

    Science.gov (United States)

    Hayden, John A.; Plock, Carl E.

    1976-01-01

    In this invention a first solution obtained from such as a plutonium/thorium purification process or the like, containing plutonium (Pu) and/or thorium (Th) in such as a low nitric acid (HNO.sub.3) concentration may have the Pu and/or Th separated and concentrated by passing an electrical current from a first solution having disposed therein an anode to a second solution having disposed therein a cathode and separated from the first solution by a cation permeable membrane, the Pu or Th cation permeating the cation membrane and forming an anionic complex within the second solution, and electrical current passage affecting the complex formed to permeate an anion membrane separating the second solution from an adjoining third solution containing disposed therein an anode, thereby effecting separation and concentration of the Pu and/or Th in the third solution.

  3. Computer simulations for thorium doped tungsten crystals

    Energy Technology Data Exchange (ETDEWEB)

    Eberhard, Bernd

    2009-07-17

    Tungsten has the highest melting point among all metals in the periodic table of elements. Furthermore, its equilibrium vapor pressure is by far the lowest at the temperature given. Thoria, ThO{sub 2}, as a particle dopant, results in a high temperature creep resistant material. Moreover, thorium covered tungsten surfaces show a drastically reduced electronic work function. This results in a tremendous reduction of tip temperatures of cathodes in discharge lamps, and, therefore, in dramatically reduced tungsten vapor pressures. Thorium sublimates at temperatures below those of a typical operating cathode. For proper operation, a diffusional flow of thorium atoms towards the surface has to be maintained. This atomic flux responds very sensitively on the local microstructure, as grain boundaries as well as dislocation cores offer ''short circuit paths'' for thorium atoms. In this work, we address some open issues of thoriated tungsten. A molecular dynamics scheme (MD) is used to derive static as well as dynamic material properties which have their common origin in the atomistic behavior of tungsten and thorium atoms. The interatomic interactions between thorium and tungsten atoms are described within the embedded atom model (EAM). So far, in literature no W-Th interaction potentials on this basis are described. As there is no alloying system known between thorium and tungsten, we have determined material data for the fitting of these potentials using ab-initio methods. This is accomplished using the full potential augmented plane wave method (FLAPW), to get hypothetical, i.e. not occurring in nature, ''alloy'' data of W-Th. In order to circumvent the limitations of classical (NVE) MD schemes, we eventually couple our model systems to external heat baths or volume reservoirs (NVT, NPT). For the NPT ensemble, we implemented a generalization of the variable cell method in combination with the Langevin piston, which results in a

  4. Self-Sustaining Thorium Boiling Water Reactors

    Energy Technology Data Exchange (ETDEWEB)

    Greenspan, Ehud [Univ. of California, Berkeley, CA (United States); Gorman, Phillip M. [Univ. of California, Berkeley, CA (United States); Bogetic, Sandra [Univ. of California, Berkeley, CA (United States); Seifried, Jeffrey E. [Univ. of California, Berkeley, CA (United States); Zhang, Guanheng [Univ. of California, Berkeley, CA (United States); Varela, Christopher R. [Univ. of California, Berkeley, CA (United States); Fratoni, Massimiliano [Univ. of California, Berkeley, CA (United States); Vijic, Jasmina J. [Univ. of California, Berkeley, CA (United States); Downar, Thomas [Univ. of Michigan, Ann Arbor, MI (United States); Hall, Andrew [Univ. of Michigan, Ann Arbor, MI (United States); Ward, Andrew [Univ. of Michigan, Ann Arbor, MI (United States); Jarrett, Michael [Univ. of Michigan, Ann Arbor, MI (United States); Wysocki, Aaron [Univ. of Michigan, Ann Arbor, MI (United States); Xu, Yunlin [Univ. of Michigan, Ann Arbor, MI (United States); Kazimi, Mujid [Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States); Shirvan, Koroush [Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States); Mieloszyk, Alexander [Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States); Todosow, Michael [Brookhaven National Lab. (BNL), Upton, NY (United States); Brown, Nicolas [Brookhaven National Lab. (BNL), Upton, NY (United States); Cheng, Lap [Brookhaven National Lab. (BNL), Upton, NY (United States)

    2015-03-15

    The primary objectives of this project are to: Perform a pre-conceptual design of a core for an alternative to the Hitachi proposed fuel-self- sustaining RBWR-AC, to be referred to as a RBWR-Th. The use of thorium fuel is expected to assure negative void coefficient of reactivity (versus positive of the RBWR-AC) and improve reactor safety; Perform a pre-conceptual design of an alternative core to the Hitachi proposed LWR TRU transmuting RBWR-TB2, to be referred to as the RBWR-TR. In addition to improved safety, use of thorium for the fertile fuel is expected to improve the TRU transmutation effectiveness; Compare the RBWR-Th and RBWR-TR performance against that of the Hitachi RBWR core designs and sodium cooled fast reactor counterparts - the ARR and ABR; and, Perform a viability assessment of the thorium-based RBWR design concepts to be identified along with their associated fuel cycle, a technology gap analysis, and a technology development roadmap. A description of the work performed and of the results obtained is provided in this Overview Report and, in more detail, in the Attachments. The major findings of the study are summarized.

  5. Thorium: in search of a global solution

    CERN Multimedia

    Antonella Del Rosso

    2013-01-01

    Last week, an international conference held at CERN brought together the world’s main experts in the field of alternative nuclear technology for the first time to discuss the use of thorium for the production of energy and the destruction of nuclear waste. Among the different technologies presented and discussed at the conference was ADS (Accelerator-Driven Systems) which relies primarily on particle accelerators.   The conference Chair (far left), the organisers and some of the distinguished participants of the ThEC13 conference held at CERN from 27 to 31 October 2013. “CERN has always been interested in finding ways in which fundamental research can help to resolve the problems of society,” says Jean-Pierre Revol, a physicist at the ALICE experiment who recently retired from CERN and is President of iThEC, the international not-for-profit organisation which promotes research and development in the field of thorium and which organised the Thorium Energy 2013 (Th...

  6. Electronic structure of eka-thorium (element 122) compared with thorium

    Energy Technology Data Exchange (ETDEWEB)

    Eliav, Ephraim; Landau, Arie; Kaldor, Uzi [School of Chemistry, Tel Aviv University, Tel Aviv (Israel)]. E-mail: kaldor@jade.tau.ac.il; Ishikawa, Yasuyuki [Department of Chemistry, University of Puerto Rico, San Juan, Puerto Rico (United States)

    2002-04-14

    The electronic levels of thorium and eka-thorium (element 122) are calculated in the framework of the Dirac-Coulomb-Breit Hamiltonian using a large Gaussian-spinor basis. Correlation is included by the Fock-space or intermediate Hamiltonian coupled-cluster method. The 51 reported levels of thorium and its ions are compared with experiment, giving an average error of 0.062 V for Fock space and 0.051 V for the intermediate Hamiltonian method. Predicted E122 levels are expected to have similar accuracy. The ground state of E122 is 8s{sup 2}7d8p, to be contrasted with 7s{sup 2}6d{sup 2} for Th. Increased relativistic effects in the super-heavy element lead to major differences between the level structure of these two atoms and their ions. The effects of Breit and QED terms are discussed. (author)

  7. 230Th-234U Age-Dating Uranium by Mass Spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Williams, R W; Gaffney, A M

    2012-04-18

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

  8. Uranium-series constraints on radionuclide transport and groundwater flow at the Nopal I uranium deposit, Sierra Pena Blanca, Mexico.

    Science.gov (United States)

    Goldstein, Steven J; Abdel-Fattah, Amr I; Murrell, Michael T; Dobson, Patrick F; Norman, Deborah E; Amato, Ronald S; Nunn, Andrew J

    2010-03-01

    Uranium-series data for groundwater samples from the Nopal I uranium ore deposit were obtained to place constraints on radionuclide transport and hydrologic processes for a nuclear waste repository located in fractured, unsaturated volcanic tuff. Decreasing uranium concentrations for wells drilled in 2003 are consistent with a simple physical mixing model that indicates that groundwater velocities are low ( approximately 10 m/y). Uranium isotopic constraints, well productivities, and radon systematics also suggest limited groundwater mixing and slow flow in the saturated zone. Uranium isotopic systematics for seepage water collected in the mine adit show a spatial dependence which is consistent with longer water-rock interaction times and higher uranium dissolution inputs at the front adit where the deposit is located. Uranium-series disequilibria measurements for mostly unsaturated zone samples indicate that (230)Th/(238)U activity ratios range from 0.005 to 0.48 and (226)Ra/(238)U activity ratios range from 0.006 to 113. (239)Pu/(238)U mass ratios for the saturated zone are 1000 times lower than the U mobility. Saturated zone mobility decreases in the order (238)U approximately (226)Ra > (230)Th approximately (239)Pu. Radium and thorium appear to have higher mobility in the unsaturated zone based on U-series data from fractures and seepage water near the deposit.

  9. Uranium-series constraints on radionuclide transport and groundwater flow at the Nopal I uranium deposit, Sierra Pena Blanca, Mexico

    Energy Technology Data Exchange (ETDEWEB)

    Goldstein, S.J.; Abdel-Fattah, A.I.; Murrell, M.T.; Dobson, P.F.; Norman, D.E.; Amato, R.S.; Nunn, A. J.

    2009-10-01

    Uranium-series data for groundwater samples from the Nopal I uranium ore deposit were obtained to place constraints on radionuclide transport and hydrologic processes for a nuclear waste repository located in fractured, unsaturated volcanic tuff. Decreasing uranium concentrations for wells drilled in 2003 are consistent with a simple physical mixing model that indicates that groundwater velocities are low ({approx}10 m/y). Uranium isotopic constraints, well productivities, and radon systematics also suggest limited groundwater mixing and slow flow in the saturated zone. Uranium isotopic systematics for seepage water collected in the mine adit show a spatial dependence which is consistent with longer water-rock interaction times and higher uranium dissolution inputs at the front adit where the deposit is located. Uranium-series disequilibria measurements for mostly unsaturated zone samples indicate that {sup 230}Th/{sup 238}U activity ratios range from 0.005-0.48 and {sup 226}Ra/{sup 238}U activity ratios range from 0.006-113. {sup 239}Pu/{sup 238}U mass ratios for the saturated zone are <2 x 10{sup -14}, and Pu mobility in the saturated zone is >1000 times lower than the U mobility. Saturated zone mobility decreases in the order {sup 238}U{approx}{sup 226}Ra > {sup 230}Th{approx}{sup 239}Pu. Radium and thorium appear to have higher mobility in the unsaturated zone based on U-series data from fractures and seepage water near the deposit.

  10. Updated determination of particulate and dissolved thorium-234

    Science.gov (United States)

    Fleer, Alan P.

    The determination of particulate and dissolved 234Th is similar to the procedure of Anderson and Fleer [1982]. Samples are collected using 30 L Niskin bottles with Teflon- or epoxy-coated internal springs. On deck, the sample is pumped with a delrin impeller pump through a 0.45 μm pore size 147-mm diameter Millipore filter and into a pre-rinsed 6 gallon plastic cubitainer held in a plastic milk crate. An in-line plastic water meter records volumes in gallons. The particulate sample filter is folded twice and stored in a polyethylene sample bag. To the ˜20 L filtered sample is added: 30 mL reagent grade 16 N HNO3; 500 mL 230Th tracer of ˜30 dpm mL-l and 5 mL 50 mg mL-l iron carrier previously cleaned by extraction into isopropyl ether from an 8 M HCl solution and back-extracted into 0.1 M HCl. The acidified sample is allowed to equilibrate for from one day to a maximum of several days. The sample is weighed on a Heathkit digital scale and the pH is adjusted to approximately 8 with about 40 mL 10 M NH4OH to precipitate iron hydroxide, which carries the thorium and uranium from the solution. The precipitate is allowed to settle for 12 to 24 hours. The supernate is drawn off, and the precipitate is spun down in a centrifuge tube to about an 8 mL volume. The precipitate is resuspended in distilled water and spun down again, then dissolved in three times its volume with 12 N HCl to make a 9 N HCl solution. A 1.5 cm×12 cm ion exchange column is filled with AG1×8 100-200 mesh resin and conditioned with 9 N HCl. The sample solution is run slowly through.

  11. Uranium provinces of North America; their definition, distribution, and models

    Science.gov (United States)

    Finch, Warren Irvin

    1996-01-01

    Uranium resources in North America are principally in unconformity-related, quartz-pebble conglomerate, sandstone, volcanic, and phosphorite types of uranium deposits. Most are concentrated in separate, well-defined metallogenic provinces. Proterozoic quartz-pebble conglomerate and unconformity-related deposits are, respectively, in the Blind River–Elliot Lake (BRELUP) and the Athabasca Basin (ABUP) Uranium Provinces in Canada. Sandstone uranium deposits are of two principal subtypes, tabular and roll-front. Tabular sandstone uranium deposits are mainly in upper Paleozoic and Mesozoic rocks in the Colorado Plateau Uranium Province (CPUP). Roll-front sandstone uranium deposits are in Tertiary rocks of the Rocky Mountain and Intermontane Basins Uranium Province (RMIBUP), and in a narrow belt of Tertiary rocks that form the Gulf Coastal Uranium Province (GCUP) in south Texas and adjacent Mexico. Volcanic uranium deposits are concentrated in the Basin and Range Uranium Province (BRUP) stretching from the McDermitt caldera at the Oregon-Nevada border through the Marysvale district of Utah and Date Creek Basin in Arizona and south into the Sierra de Peña Blanca District, Chihuahua, Mexico. Uraniferous phosphorite occurs in Tertiary sediments in Florida, Georgia, and North and South Carolina and in the Lower Permian Phosphoria Formation in Idaho and adjacent States, but only in Florida has economic recovery been successful. The Florida Phosphorite Uranium Province (FPUP) has yielded large quantities of uranium as a byproduct of the production of phosphoric acid fertilizer. Economically recoverable quantities of copper, gold, molybdenum, nickel, silver, thorium, and vanadium occur with the uranium deposits in some provinces.Many major epochs of uranium mineralization occurred in North America. In the BRELUP, uranium minerals were concentrated in placers during the Early Proterozoic (2,500–2,250 Ma). In the ABUP, the unconformity-related deposits were most likely

  12. Economics and utilization of thorium in nuclear reactors

    Energy Technology Data Exchange (ETDEWEB)

    1978-05-01

    Information on thorium utilization in power reactors is presented concerning the potential demand for nuclear power, the potential supply for nuclear power, economic performance of thorium under different recycle policies, ease of commercialization of the economically preferred cases, policy options to overcome institutional barriers, and policy options to overcome technological and regulatory barriers.

  13. Assessment of Thorium in the Environment (A Review)

    National Research Council Canada - National Science Library

    Bhatti, Ijaz Ahmad; Hayat, Mohammad Atique; Iqbal, Munawar

    2012-01-01

    ... a fraction of thorium to be released in the environment eventually. This review focuses on the radiochemical techniques, such as alpha, gamma spectroscopy as well as inductively coupled plasma mass spectrometry (ICP-MS) that are used for the measurement of thorium. A survey of current research activities intend to control the incorporation ...

  14. Evaluation of thorium based nuclear fuel. Chemical aspects

    Energy Technology Data Exchange (ETDEWEB)

    Konings, R.J.M.; Blankenvoorde, P.J.A.M.; Cordfunke, E.H.P.; Bakker, K.

    1995-07-01

    This report describes the chemical aspects of a thorium-based fuel cycle. It is part of a series devoted to the study of thorium-based fuel as a means to achieve a considerable reduction of the radiotoxicity of the waste from nuclear power production. Therefore special emphasis is placed on fuel (re-)fabrication and fuel reprocessing in the present work. (orig.).

  15. Study of the thorium phosphate-diphosphate (TPD) dissolution: kinetic aspect - thermodynamic aspect: analysis of the neo-formed phases; Etude de la dissolution du phosphate diphosphate de thorium: - aspect cinetique - aspect thermodynamique: analyse des phases neoformees

    Energy Technology Data Exchange (ETDEWEB)

    Thomas, A.Ch

    2000-10-06

    The aim of this work is to study the aqueous corrosion of the thorium phosphate-diphosphate (TPD), of the formula Th{sub 4}(PO{sub 4}){sub 4}P{sub 2}O{sub 7}, in the framework of the actinides immobilization. In order to complete the anterior studies concerning solid solutions where thorium is substituted by a tetravalent ion (uranium (IV) or plutonium (IV)) in the TPD structure, compounds of thorium and neptunium phosphate-diphosphate, of formula Th{sub 4-x}Np{sub x}(PO{sub 4}){sub 4}P{sub 2}O{sub 7}, have been prepared. Furthermore, a new chemical way of synthesis has been investigated in order to sinter solids solution of thorium and uranium phosphate-diphosphate (TUPD) in good conditions. The TPD dissolution study showed two principals steps. The first one corresponds to the control of element concentration by the material dissolution whereas the second corresponds to the formation of secondary precipitates for which thermodynamic equilibrium controls the concentration of the species in solution. Leaching tests have been performed varying several independent parameters in order to determine the TPD dissolution rate. The partial orders related to the protons or to the hydroxide ions have been found between 0.35 and 0.45 whereas the apparent dissolution rate constants are in the range 1.10{sup -5} for 9.10{sup -5} g.m{sup -2}.j{sup -1} for acidic and basic media. The neo-formed phases have been characterized after the dissolution of TPD and TUPD. We found that the TPD leaching in acidic medium leads to the formation of the crystallized thorium phosphate-hydrogen-phosphate (TPHP), of formula Th{sub 2}(PO{sub 4}){sub 2}(HPO{sub 4}), x H{sub 2}O, whereas the TUPD dissolution leads to the TPHP and an other compound, of formula (UO{sub 2}){sub 3}(PO{sub 4}){sub 2}, 5 H{sub 2}O. We calculated its solubility product which is in good agreement with those found in the literature. The phases formed during the leaching of solids containing plutonium; americium or curium (Th

  16. Design and Analysis of Thorium-fueled Reduced Moderation Boiling Water Reactors

    Science.gov (United States)

    Gorman, Phillip Michael

    The Resource-renewable Boiling Water Reactors (RBWRs) are a set of light water reactors (LWRs) proposed by Hitachi which use a triangular lattice and high void fraction to incinerate fuel with an epithermal spectrum, which is highly atypical of LWRs. The RBWRs operate on a closed fuel cycle, which is impossible with a typical thermal spectrum reactor, in order to accomplish missions normally reserved for sodium fast reactors (SFRs)--either fuel self-sufficiency or waste incineration. The RBWRs also axially segregate the fuel into alternating fissile "seed" regions and fertile "blanket" regions in order to enhance breeding and leakage probability upon coolant voiding. This dissertation focuses on thorium design variants of the RBWR: the self-sufficient RBWR-SS and the RBWR-TR, which consumes reprocessed transuranic (TRU) waste from PWR used nuclear fuel. These designs were based off of the Hitachi-designed RBWR-AC and the RBWR-TB2, respectively, which use depleted uranium (DU) as the primary fertile fuel. The DU-fueled RBWRs use a pair of axially segregated seed sections in order to achieve a negative void coefficient; however, several concerns were raised with this multi-seed approach, including difficulty with controlling the reactor and unacceptably high axial power peaking. Since thorium-uranium fuel tends to have much more negative void feedback than uranium-plutonium fuels, the thorium RBWRs were designed to use a single elongated seed to avoid these issues. A series of parametric studies were performed in order to find the design space for the thorium RBWRs, and optimize the designs while meeting the required safety constraints. The RBWR-SS was optimized to maximize the discharge burnup, while the RBWR-TR was optimized to maximize the TRU transmutation rate. These parametric studies were performed on an assembly level model using the MocDown simulator, which calculates an equilibrium fuel composition with a specified reprocessing scheme. A full core model was

  17. Design study of Thorium-232 and Protactinium-231 based fuel for long life BWR

    Science.gov (United States)

    Trianti, N.; Su'ud, Z.; Riyana, E. S.

    2012-06-01

    A preliminary design study for the utilization of thorium added with 231Pa based fuel on BWR type reactor has been performed. In the previous research utilization of fuel based Thorium-232 and Uranium-233 show 10 years operation time with maximum excess-reactivity about 4.075% dk/k. To increase reactor operation time and reduce excess-reactivity below 1% dk/k, Protactinium (Pa-231) is used as Burnable Poison. Protactinium-231 has very interesting neutronic properties, which enable the core to reduce initial excess-reactivity and simultaneously increase production of 233U to 231Pa in burn-up process. Optimizations of the content of 231Pa in the core enables the BWR core to sustain long period of operation time with reasonable burn-up reactivity swing. Based on the optimization of fuel element composition (Th and Pa) in various moderation ratio we can get reactor core with longer operation time, 20 ˜ 30 years operation without fuel shuffling or refuelling, with average power densities maximum of about 35 watt/cc, and maximum excess-reactivity 0.56% dk/k.

  18. Naturally occurring radionuclides in food and drinking water from a thorium-rich area

    Energy Technology Data Exchange (ETDEWEB)

    Costa Lauria, Dejanira da; Rochedo, Elaine R.R.; Godoy, Maria Luisa D.P.; Santos, Eliane E. [Brazilian Nuclear Energy Commission, Instituto de Radioprotecao e Dosimetria, Rio de Janeiro (Brazil); Hacon, Sandra S. [Oswaldo Cruz Foundation, Escola Nacional de Saude Publica, Rio de Janeiro (Brazil)

    2012-11-15

    This paper focuses on a survey of uranium and thorium decay chain radionuclides in food and drinking water from the thorium-rich (monazite-bearing) region of Buena, which is located in the state of Rio de Janeiro, Brazil. The radionuclide concentration values in the food and drinking water from Buena reached values higher than 100-fold the international reference values. The daily intake of radionuclides by the local population is similar to that of another high background radiation area in Brazil, but the intake is higher than that of residents from a normal background radiation area. Approximately 58 % of the food consumed by Buena inhabitants is produced locally. Based on that figure, locally produced food and the dilution of total radionuclides in the diet of residents caused by food importation are both highly relevant to a population's intake of radionuclides. The concentration values for {sup 210}Pb and the radium isotopes in drinking water from Buena are among the highest values to be reported in the literature. {sup 228}Ra is the most important radionuclide ingested with both food and water among the inhabitants of Buena. (orig.)

  19. Synthesis of ion-exchange resin for selective thorium and uranyl ions sorption

    Science.gov (United States)

    Konovalov, Konstantin; Sachkov, Victor

    2017-11-01

    In this work, the method of ion-exchange resin synthesis selective to radionuclides (uranium and thorium) is presented. The method includes synthesis of polymeric styrene-divinylbenzene macroporous matrix with size of 0.1-0.2 mm, and its subsequent transformation by nitration and then reduction by tin (II) chloride. For passivation of active primary amines partially oxidation by oxygen from air is used. Obtained ion-exchange resin has ratio of sorption sum U+Th to sorption sum of other total rare-earth elements as 1:1.88 at ratio of solid to liquid phase 1:200. The proposed method of ion-exchange resin synthesis is scaled-up for laboratory reactors with volume of 5 and 50 liters.

  20. Electronic States in Thorium under Pressure

    DEFF Research Database (Denmark)

    Skriver, Hans Lomholt; Jan, J. P.

    1980-01-01

    We have used the local-density formalism and the atomic-sphere approximation to calculate self-consistently the electronic properties of thorium at pressures up to 400 kbar. The derived equation of state agrees very well with static pressure experiments and shock data. Below the Fermi level (EF......) the electronic band structure is formed by 7s and 6d states while the bottom of a relatively broad 5f band is positioned 0.07 Ry above EF. The calculated extremal areas of the Fermi surface and their calculated pressure dependence agree with earlier calculations and with de Haas-van Alphen measurements...

  1. 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.

  2. Uranium, mining and hydrogeology

    Energy Technology Data Exchange (ETDEWEB)

    Merkel, Broder J. [TU Bergakademie Freiberg (Germany). Inst. fuer Geologie; Hasche-Berger, Andrea (eds.) [TU Bergakademie Freiberg (Germany). Inst. fuer Geophysik

    2008-07-01

    Subject of the book is Uranium and its migration in aquatic environments. The following subjects are emphasised: Uranium mining, Phosphate mining, mine closure and remediation, Uranium in groundwater and in bedrock, biogeochemistry of Uranium, environmental behavior, and modeling. Particular results from the leading edge of international research are presented. (orig.)

  3. Uranium processing and properties

    CERN Document Server

    2013-01-01

    Covers a broad spectrum of topics and applications that deal with uranium processing and the properties of uranium Offers extensive coverage of both new and established practices for dealing with uranium supplies in nuclear engineering Promotes the documentation of the state-of-the-art processing techniques utilized for uranium and other specialty metals

  4. Weathering and transport of sediments in the Bolivian Andes : time constraints from uranium-series isotopes

    OpenAIRE

    Dosseto, A.; Bourdon, B.; Gaillardet, J.; Maurice Bourgoin, Laurence; Allegre, C.J.

    2006-01-01

    Rivers from the upper Rio Madeira basin (Bolivia) have been studied with uranium-series isotopes in order to constrain the timescales of weathering and sediment transfer from the Andes through the Amazon tropical plain. Uranium (U), thorium, (Th) and radium (Ra) isotopes (U-238-U-234-Th-230-Ra-226 and Th-232) have been analyzed in the suspended load (> 0.2 mu m) of rivers. Increasing Th-230 excesses relative to U-238 in suspended particles from the Andes to the tropical plain is interpreted a...

  5. URANIUM DECONTAMINATION

    Science.gov (United States)

    Buckingham, J.S.; Carroll, J.L.

    1959-12-22

    A process is described for reducing the extractability of ruthenium, zirconium, and niobium values into hexone contained in an aqueous nitric acid uranium-containing solution. The solution is made acid-deficient, heated to between 55 and 70 deg C, and at that temperature a water-soluble inorganic thiosulfate is added. By this, a precipitate is formed which carries the bulk of the ruthenium, and the remainder of the ruthenium as well as the zirconium and niobium are converted to a hexone-nonextractable form. The rutheniumcontaining precipitate can either be removed from the solu tion or it can be dissolved as a hexone-non-extractable compound by the addition of sodium dichromate prior to hexone extraction.

  6. Uranium series geochemistry in aquifers: quantification of transport mechanisms of uranium and daughter products: the chalk aquifer (Champagne, France); Desequilibres des series de l'uranium dans les aquiferes: quantification des mecanismes de transport de l'uranium et de ses descendants: cas de l'aquifere de la craie (Champagne, France)

    Energy Technology Data Exchange (ETDEWEB)

    Hubert, A

    2005-09-15

    With the increase of contaminant flux of radionuclides in surface environment (soil, river, aquifer...), there is a need to understand and model the processes that control the distribution of uranium and its daughter products during transport within aquifers. We have used U-series disequilibria as an analogue for the transport of uranium and its daughter products in aquifer to understand such mechanisms. The measurements of uranium ({sup 234}U et {sup 238}U), thorium ({sup 230}Th et {sup 232}Th), {sup 226}Ra and {sup 222}Rn isotopes in the solid and liquid phases of the chalk aquifer in Champagne (East of France) allows us to understand the processes responsible for fractionation within the uranium decay chain. Fractionations are induced by physical and chemical properties of the elements (leaching, adsorption) but also by radioactive properties (recoil effect during {alpha}-decay). For the first time a comprehensive sampling of the solid phase has been performed, allowing quantifying mechanisms responsible for the long term evolution of the aquifer. A non steady state 1D model has been developed which takes into account leaching, adsorption processes as well as radioactive filiation and {alpha}-recoil effect. Retardation coefficients have been calculated for uranium, thorium and radium. The aquifer is characterised by a double porosity, and the contribution of fracture and matrix porosity on the water/rock interaction processes has been estimated. (author)

  7. Geochemical orientation survey of stream sediment, stream water, and ground water near uranium prospects, Monticello area, New York. National Uranium Resource Evaluation Program

    Energy Technology Data Exchange (ETDEWEB)

    Rose, A. W.; Smith, A. T.; Wesolowski, D.

    1982-08-01

    A detailed geochemical test survey has been conducted in a 570 sq km area around six small copper-uranium prospects in sandstones of the Devonian Catskill Formation near Monticello in southern New York state. This report summarizes and interprets the data for about 500 stream sediment samples, 500 stream water samples, and 500 ground water samples, each analyzed for 40 to 50 elements. The groundwater samples furnish distinctive anomalies for uranium, helium, radon, and copper near the mineralized localities, but the samples must be segregated into aquifers in order to obtain continuous well-defined anomalies. Two zones of uranium-rich water (1 to 16 parts per billion) can be recognized on cross sections; the upper zone extends through the known occurrences. The anomalies in uranium and helium are strongest in the deeper parts of the aquifers and are diluted in samples from shallow wells. In stream water, copper and uranium are slightly anomalous, as in an ore factor derived from factor analysis. Ratios of copper, uranium, and zinc to conductivity improve the resolution of anomalies. In stream sediment, extractable uranium, copper, niobium, vanadium, and an ore factor furnish weak anomalies, and ratios of uranium and copper to zinc improve the definition of anomalies. The uranium/thorium ratio is not helpful. Published analyses of rock samples from the nearby stratigraphic section show distinct anomalies in the zone containing the copper-uranium occurrences. This report is being issued without the normal detailed technical and copy editing, to make the data available to the public before the end of the National Uranium Reconnaissance Evaluation program.

  8. Uranium industry annual 1994

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-07-05

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

  9. Extraction of some strategic elements from thorium–uranium concentrate using bioproducts of Aspergillus ficuum and Pseudomonas aeruginosa

    Directory of Open Access Journals (Sweden)

    Osman A. Desouky

    2016-09-01

    Full Text Available The activity of the bioproducts from Aspergillus ficuum and Pseudomonas aeruginosa for extraction of thorium (Th4+, uranium (UO22+ and rare earth elements (REEs from thorium–uranium concentrate was studied. P. aeruginosa produce element-specific ligand (siderophore that is able to change pH and enhance chelation of Th4+ and UO22+. The produced siderophore at pH 5.3 has the ability to bioleach and is complexed with 68.00% of uranium and 65.00% of thorium. Also, A. ficuum produced different kinds of organic acids which leached 30.00% of uranium and 29.12% of thorium in addition to 20.00% of lanthanum, 33.00% of cerium and 2.51% of yttrium as rare earth elements at pH 3.0. Oxalic acid was efficient for Th4+, UO22+and REEs precipitation. The binocular stereo-microscope (BSM, environmental scanning electron microscope (ESEM and X-ray diffraction (XRD analyses confirmed the percentages of extracted metals. Exogenous polysaccharides (EPSs seem to play an important role in bioleaching and removal of these elements. It was found that EPSs produced by A. ficuum adsorbed Th4+, UO22+ and REEs while that produced by P. aeruginosa adsorbed REEs only.

  10. URANIUM RECOVERY PROCESS

    Science.gov (United States)

    Bailes, R.H.; Long, R.S.; Olson, R.S.; Kerlinger, H.O.

    1959-02-10

    A method is described for recovering uranium values from uranium bearing phosphate solutions such as are encountered in the manufacture of phosphate fertilizers. The solution is first treated with a reducing agent to obtain all the uranium in the tetravalent state. Following this reduction, the solution is treated to co-precipitate the rcduced uranium as a fluoride, together with other insoluble fluorides, thereby accomplishing a substantially complete recovery of even trace amounts of uranium from the phosphate solution. This precipitate usually takes the form of a complex fluoride precipitate, and after appropriate pre-treatment, the uranium fluorides are leached from this precipitate and rccovered from the leach solution.

  11. Economics of large-scale thorium oxide production: assessment of domestic resources

    Energy Technology Data Exchange (ETDEWEB)

    Young, J.K.; Bloomster, C.H.; Enderlin, W.I.; Morgenstern, M.H.; Ballinger, M.Y.; Drost, M.K.; Weakley, S.A.

    1980-02-01

    The supply curve illustrates that sufficient amounts of thorium exist supply a domestic thorium-reactor economy. Most likely costs of production range from $3 to $60/lb ThO/sub 2/. Near-term thorium oxide resources include the stockpiles in Ohio, Maryland, and Tennessee and the thorite deposits at Hall Mountain, Idaho. Costs are under $10/lb thorium oxide. Longer term economic deposits include Wet Mountain, Colorado; Lemhi Pass, Idaho; and Palmer, Michigan. Most likely costs are under $20/lb thorium oxide. Long-term deposits include Bald Mountain, Wyoming; Bear Lodge, Wyoming; and Conway, New Hampshire. Costs approximately equal or exceed $50/lb thorium oxide.

  12. The influence of different hydroponic conditions on thorium uptake by Brassica juncea var. foliosa.

    Science.gov (United States)

    Wang, Dingna; Zhou, Sai; Liu, Li; Du, Liang; Wang, Jianmei; Huang, Zhenling; Ma, Lijian; Ding, Songdong; Zhang, Dong; Wang, Ruibing; Jin, Yongdong; Xia, Chuanqin

    2015-05-01

    The effects of different hydroponic conditions (such as concentration of thorium (Th), pH, carbonate, phosphate, organic acids, and cations) on thorium uptake by Brassica juncea var. foliosa were evaluated. The results showed that acidic cultivation solutions enhanced thorium accumulation in the plants. Phosphate and carbonate inhibited thorium accumulation in plants, possibly due to the formation of Th(HPO4)(2+), Th(HPO4)2, or Th(OH)3CO3 (-) with Th(4+), which was disadvantageous for thorium uptake in the plants. Organic aids (citric acid, oxalic acid, lactic acid) inhibited thorium accumulation in roots and increased thorium content in the shoots, which suggested that the thorium-organic complexes did not remain in the roots and were beneficial for thorium transfer from the roots to the shoots. Among three cations (such as calcium ion (Ca(2+)), ferrous ion (Fe(2+)), and zinc ion (Zn(2+))) in hydroponic media, Zn(2+) had no significant influence on thorium accumulation in the roots, Fe(2+) inhibited thorium accumulation in the roots, and Ca(2+) was found to facilitate thorium accumulation in the roots to a certain extent. This research will help to further understand the mechanism of thorium uptake in plants.

  13. Synthesis of uranium fluorides from uranium dioxide with ammonium bifluoride and ammonolysis of uranium fluorides to uranium nitrides

    Science.gov (United States)

    Yeamans, Charles Burnett

    This work presents the chemical conversion of uranium oxides to uranium fluorides, and their subsequent conversion to uranium nitrides. Uranium dioxide reacts with ammonium bifluoride at 20°C to form compound in the ammonium-uranium fluoride chemical system. This reaction occurs between solid uranium dioxide at the surface of the particles and ammonium fluoride vapor. A shrinking-sphere model demonstrated surface reaction kinetics, not mass transport by diffusion through the product layer, limit the reaction rate when the starting material consists of 100 mum uranium dioxide particles. Powder x-ray diffraction showed the reaction to be complete within 8 hours, with (NH4) 4UF8 the reaction product. High-resolution electron microcopy revealed the product is largely amorphous on a micrometer-scale, but contains well-formed crystal domains on the order of 10x10 nm. X-ray diffraction showed the reaction progresses though beta-NH4UF5, delta-(NH 4)2UF6, and gamma-(NH4)2UF6 intermediate phases before finally forming (NH4)4UF 8. Modeling the system as a series of first-order reaction suggested a fourth intermediate, possibly UF4, is likely to occur. The reaction of (NH4)4UF8 with ammonia gas at 800°C forms alpha-U2N3/UN2 solid solution products with a composition of UN1.83. The x-ray powder diffraction pattern of this product is the fcc pattern commonly referenced as that of UN2 and the lattice parameter was 0.53050 nm. Surface area increased by a factor of ten during ammonolysis, consistent with the action of a hydriding agent. The alpha-U2N 3/UN2 solid solution system formed contained 1 wt% UO 2 as an impurity. Upon subsequent heating to 1150°C for 4.5 hours under argon, the nitride sample formed UN with a UO2 impurity of 9 wt%. Based on the HRTEM images, oxidation in the UN product appears to be limited to within 20 nm of particle surfaces and grain boundaries.

  14. Uranium Processing Facility

    Data.gov (United States)

    Federal Laboratory Consortium — An integral part of Y‑12's transformation efforts and a key component of the National Nuclear Security Administration's Uranium Center of Excellence, the Uranium...

  15. Cathodoluminescence of uranium oxides

    Energy Technology Data Exchange (ETDEWEB)

    Winer, K.; Colmenares, C.; Wooten, F.

    1984-08-09

    The cathodoluminescence of uranium oxide surfaces prepared in-situ from clean uranium exposed to dry oxygen was studied. The broad asymmetric peak observed at 470 nm is attributed to F-center excitation.

  16. Uranium mining: Saskatchewan status

    Energy Technology Data Exchange (ETDEWEB)

    Martin, V. [AREVA Resources Canada Inc., Saskatoon, Saskatchewan, Ontario (Canada)

    2012-07-01

    This paper gives the status of uranium mining by Areva in Saskatchewan. Uranium production now meets 85% of world demand for power generation. 80% of world production of uranium comes from top 5 countries: Kazakhstan, Canada, Australia, Niger and Namibia. Saskatchewan is currently the only Canadian province with active uranium mines and mills and the largest exploration programs. Several mine projects are going through the environmental assessment process. Public opinion is in favour of mining activities in Saskatchewan.

  17. Valence electronic state density in thorium dioxide

    Directory of Open Access Journals (Sweden)

    Teterin Anton Yu.

    2008-01-01

    Full Text Available This work analyses the fine low energy (0-40 eV X-ray photoelectron spectra of ThO2, taking into account relativistic Xα-discrete variation electronic structure calculations for the ThO8 (D4h cluster reflecting thorium's close environment in ThO2. As a result, it was theoretically shown and experimentally confirmed that Th5f electrons in ThO2 can participate directly (~0.6 Th5f electrons in chemical bond formation.Th6p electrons were shown to be a significant part (~0.44 Th6p electrons not only of inner valence molecular orbitals, but to play a significant role in outer valence molecular orbitals formation, as well. Inner valence molecular orbitals composition and sequent order were established to belong to the binding energy range of 13 eV to 40 eV. The valence electronic state density in the range of 0-40 eV in ThO2 was also calculated. For the first time, these data allowed an interpretation of the fine X-ray photoelectron spectra (0-40 eV and high resolution O4,5(Th X-ray emition spectral structure (~60 - ~85 eV of ThO2.

  18. Potential Radon-222 Emissions from the Thorium Nitrate Stockpile

    Energy Technology Data Exchange (ETDEWEB)

    Terry, J.W.

    2003-09-04

    The Defense National Stockpile Center (DNSC), a field level activity of the Defense Logistics Agency, has stewardship of a stockpile of thorium nitrate that has been in storage for decades. The thorium nitrate stockpile was produced from 1959 to 1964 for the Atomic Energy Commission and previously has been under the control of several federal agencies. The stockpile consists of approximately 7 million pounds of thorium nitrate crystals (hydrate form) stored at two depot locations in the United States (75% by weight at Curtis Bay, Maryland, and 25% by weight at Hammond, Indiana). The material is stored in several configurations in over 21,000 drums. The U.S. Congress has declared the entire DNSC thorium nitrate stockpile to be in excess of the needs of the Department of Defense. Part of DNSC's mission is to safely manage the continued storage, future sales, and/or disposition of the thorium nitrate stockpile. Historically, DNSC has sold surplus thorium nitrate to domestic and foreign companies, but there is no demand currently for this material. Analyses conducted by Oak Ridge National Laboratory (ORNL) in 2001 demonstrated that disposition of the thorium nitrate inventory as a containerized waste, without processing, is the least complex and lowest-cost option for disposition. A characterization study was conducted in 2002 by ORNL, and it was determined that the thorium nitrate stockpile may be disposed of as low-level waste. The Nevada Test Site (NTS) was used as a case study for the disposal alternative, and special radiological analyses and waste acceptance requirements were documented. Among the special radiological considerations is the emission of {sup 220}Rn and {sup 222}Rn from buried material. NTS has a performance objective on the emissions of radon: 20 pCi m{sup -2} sec{sup -1} at the surface of the disposal facility. The radon emissions from the buried thorium nitrate stockpile have been modeled. This paper presents background information and

  19. Chemistry of tetravalent actinides phosphates. The thorium phosphate-diphosphate as immobilisation matrix of actinides; Chimie des phosphates d'actinides tetravalents. Le phosphate-diphosphate de thorium en tant que matrice d'imobilisation des actinides

    Energy Technology Data Exchange (ETDEWEB)

    Dacheux, N

    2002-07-01

    The author presents in this document its scientific works from 1992 to 2001, in order to obtain the enabling to manage scientific and chemical researches at the university Paris Sud Orsay. The first part gives an abstract of the thesis on the characterizations, lixiviation and synthesis of uranium and thorium based phosphate matrix in the framework of the search for a ceramic material usable in the radioactive waste storage. The second part presents briefly the researches realized at the CEA, devoted to a reliable, independent and accurate measure of some isotopes activity. The last part presents the abstracts of researches activities from 1996 to 2001 on the tetravalent actinides phosphates chemistry, the sintering of PDT and solid solutions of PDTU and the kinetic and thermodynamical studies of the PDT dissolution. Many references and some publication in full text are provided. (A.L.B.)

  20. Microminiature nuclear reactor using liquid thorium fuel

    Energy Technology Data Exchange (ETDEWEB)

    Furukawa, Kazuo.

    1988-11-07

    Purpose: To provide a microminiature nuclear reactor of about 0.2 - 20,000 KW power. Constitution: A reactor core having graphite moderator disposed cylindrically therein has a volume of 200 - 3000 liter and a height/ diameter ratio of about 1.10 - 1.30, in which the inside is divided into two regions, that is, a central region I and a blanket region II. The gap ratio of the moderator in the central region I is set to about 10% and that in the blanket region II is set to about 30%. Nuclear fuel-containing salts flow through the gaps in the moderators of the central region I and the blanket region II. Uranium in the nuclear fuels causes nuclear fission to generate energy and tritium is converted into uranium by neutrons generated upon nuclear fission to continue the reaction. Critical value can be attained even if the neutron density is made uniform and low. The fuel conversion ratio is as high as 50 - 70%, design, manufacture, operation and maintenance are easy and the installation and the running costs can be saved. (Furukawa, K.).

  1. Uranium speciation in plants

    Energy Technology Data Exchange (ETDEWEB)

    Guenther, A.; Bernhard, G.; Geipel, G.; Reich, T.; Rossberg, A. [Forschungszentrum Rossendorf e.V., Inst. of Radiochemistry, Dresden (Germany); Nitsche, H. [Univ. of California at Berkeley and Lawrence Berkeley National Lab., Nuclear Sciences Div., Berkeley, CA (United States)

    2003-07-01

    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.)

  2. Recovery of Ra-223 from natural thorium irradiated by protons

    Energy Technology Data Exchange (ETDEWEB)

    Vasiliev, Aleksandr N.; Ostapenko, Valentina S. [Lomonosov Moscow State Univ. (Russian Federation); Russian Academy of Sciences, Moscow-Troitsk (Russian Federation). Inst. for Nuclear Research; Lapshina, Elena V.; Ermolaev, Stanislav V.; Zhuikov, Boris L. [Russian Academy of Sciences, Moscow-Troitsk (Russian Federation). Inst. for Nuclear Research; Danilov, Sergey S. [Lomonosov Moscow State Univ. (Russian Federation); Kalmykov, Stepan N. [Lomonosov Moscow State Univ. (Russian Federation); National Research Center ' Kurchatov Institute' (NRC ' Kurchatov Institute' ), Moscow (Russian Federation)

    2016-11-01

    Irradiation of natural thorium with medium-energy protons is considered to be a prospective approach to large-scale production of {sup 225}Ac and {sup 223}Ra. In addition to the earlier-developed method of {sup 225}Ac isolation, the present work focuses on the simultaneous recovery of {sup 223}Ra from the same thorium target. Radiochemical procedure is based on liquid-liquid extraction, cation exchange and extraction chromatography. The procedure provides separation of radium from spallation and fission products generated in the thorium target. High chemical yield (85-90%) and radionuclide purity of {sup 223}Ra (> 99.8% except {sup 224}Ra and {sup 225}Ra isotopes) have been achieved.

  3. Adsorption of thorium from aqueous solutions by perlite.

    Science.gov (United States)

    Talip, Z; Eral, M; Hiçsönmez, U

    2009-02-01

    The use of expanded perlite for the adsorption of thorium from aqueous solution by batch technique is presented. The effects of particle size, pH of the solution, initial thorium concentration, shaking time, V/m ratio and temperature were determined. It was found that the adsorption capacity increases by the increase in the pH of the suspensions. The rate of thorium adsorption on expanded perlite was observed to be fast in the first hour of the reaction time. Adsorption isotherms were expressed by Langmuir and Freundlich adsorption models and the adsorption experiments conducted at 30 +/- 1 degrees C showed that the adsorption isotherms correlated well with the Langmuir model. From the adsorption data, thermodynamic parameters such as DeltaG(o), DeltaH(o) and DeltaS(o) were calculated as a function of temperature.

  4. Alterations of thorium oxalate morphology by changing elementary precipitation conditions

    Science.gov (United States)

    Tyrpekl, V.; Beliš, M.; Wangle, T.; Vleugels, J.; Verwerft, M.

    2017-09-01

    Oxalates of actinide elements are widely used in research and industry mainly due to their low solubility in aqueous solution and easy conversion to oxide. Although thorium oxide is worldwide mostly produced by the oxalate precipitation and conversion route, the powder morphology obtained through this process is known to inhibit the packing and sintering step of the pellet production. The presented work investigates the effects of oxalate precipitation conditions on the final powder morphology. Among the precipitation conditions considered are: pH of the thorium feed solution, concentration, temperature and the order of addition (thorium solution in oxalic acid solution and vice versa) known as reverse/direct strike. Herein, we show that the morphology of the final oxalate depends significantly on the above mentioned precipitation parameters.

  5. A survey of arsenic, manganese, boron, thorium, and other toxic metals in the groundwater of a West Bengal, India neighbourhood.

    Science.gov (United States)

    Bacquart, Thomas; Bradshaw, Kelly; Frisbie, Seth; Mitchell, Erika; Springston, George; Defelice, Jeffrey; Dustin, Hannah; Sarkar, Bibudhendra

    2012-07-01

    Around 150 million people are at risk from arsenic-contaminated groundwater in India and Bangladesh. Multiple metal analysis in Bangladesh has found other toxic elements above the World Health Organization (WHO) health-based drinking water guidelines which significantly increases the number of people at risk due to drinking groundwater. In this study, drinking water samples from the Bongaon area (North 24 Parganas district, West Bengal, India) were analyzed for multiple metal contamination in order to evaluate groundwater quality on the neighbourhood scale. Each sample was analyzed for arsenic (As), boron (B), barium (Ba), chromium (Cr), manganese (Mn), molybdenum (Mo), nickel (Ni), lead (Pb), and uranium (U). Arsenic was found above the WHO health-based drinking water guideline in 50% of these tubewells. Mn and B were found at significant concentrations in 19% and 6% of these tubewells, respectively. The maps of As, Mn, and B concentrations suggest that approximately 75% of this area has no safe tubewells. The concentrations of As, Mn, B, and many other toxic elements are independent of each other. The concentrations of Pb and U were not found above WHO health-based drinking water guidelines but they were statistically related to each other (p-value = 0.001). An analysis of selected isotopes in the Uranium, Actinium, and Thorium Radioactive Decay Series revealed the presence of thorium (Th) in 31% of these tubewells. This discovery of Th, which does not have a WHO health-based drinking water guideline, is a potential public health challenge. In sum, the widespread presence and independent distribution of other metals besides As must be taken into consideration for drinking water remediation strategies involving well switching or home-scale water treatment.

  6. THE IMPACT ASSESSMENT OF THE ABANDONED URANIUM MINING EXPLOITATIONS ON ROCKS AND SOILS - ZIMBRU PERIMETER, ARAD COUNTY

    Directory of Open Access Journals (Sweden)

    DIANA M. BANU

    2016-10-01

    Full Text Available The mining exploration and exploitation, especially the activity of uranium mineralization exploration and exploitation has a negative impact on the environment by the alterations of the landscape and the degradation of the environmental factors' quality. The principal environmental factors that could be affected by mining operations resulting from uranium exploitation are: water, air, soil, population, fauna, and flora. The aim of this study is, first, to identify the sources of pollution (natural radionuclides - natural radioactive series of uranium, radium, thorium, potassium and heavy metals that are accompanying the mineralizations for two of the most important environmental factors: rocks and soils: and, second, to assess the pollution impact on those two environmental factors. In order to identify this pollutants and their impact assessment it was selected as a study case an abandoned uranium mining perimeter named the Zimbru perimeter located in Arad County, Romania.

  7. Uranium hexafluoride public risk

    Energy Technology Data Exchange (ETDEWEB)

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

    1994-08-01

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

  8. Uranium mineralization in the two mica granite of gabal Ribdab area, South Eastern Desert, Egypt.

    Science.gov (United States)

    Ibrahim, M E; Saleh, G M; Abd El-Naby, H H

    2001-12-01

    Among the different rock units in the Gabal Ribdab area, the two-mica leucogranite and muscovite pegmatitic granite are the most favourable host rocks for uranium and thorium mineralization. The muscovite pegmatitic granite shows evidence of post-magmatic alteration, e.g. Na- and K-metasomatism, whereas the two-mica leucogranite could be regarded as being fresh. The spectrometric survey revealed the presence of three enriched zones with a maximum eU content of 140 ppm and the maximum eTh is 36 ppm. Uranophane, zippeite and becquerelite are the most abundant uranium minerals. The origin of these secondary minerals is mainly related to alteration of primary minerals by the action of oxidizing fluids, mobilization of uranium and then redeposition in other forms. Redistribution by circulating meteoric waters might have taken place.

  9. Electronic structure of the actinides and their dioxides. Application to the defect formation energy and krypton solubility in uranium dioxide; Etude de la structure electronique des actinides et de leurs dioxydes. Application aux defauts ponctuels et aux gaz de fission dans le dioxyde d`uranium

    Energy Technology Data Exchange (ETDEWEB)

    Petit, T. [CEA Centre d`Etudes Nucleaires de Grenoble, 38 (France)]|[CEA Centre d`Etudes de Grenoble, 38 (France). Dept. de Thermohydraulique et de Physique

    1996-09-28

    Uranium dioxide is the standard nuclear fuel used in French h power plants. During irradiation, fission products such as krypton and xenon are created inside fuel pellets. So, gas release could become, at very high burnup, a limiting factor in the reactor exploitation. To study this subject, we have realised calculations using the Density Functional Theory (DFT) into the Local Density Approximation (LDA) and the Atomic Sphere Approximation (ASA). First, we have validated our approach by calculating cohesive properties of thorium, protactinium and uranium metals. The good agreement between our results and experimental values implies that 5f electrons are itinerant. Calculated lattice parameter, cohesive energy and bulk modulus for uranium and thorium dioxides are in very good agreement with experiment. We show that binding between uranium and oxygen atoms is not completely ionic but partially covalent. The question of the electrical conductivity still remains an open problem. We have been able to calculate punctual defect formation energies in uranium dioxide. Accordingly to experimental observations, we find that it is easier to create a defect in the oxygen sublattice than in the uranium sublattice. Finally, we have been able to predict a probable site of krypton atoms in nuclear fuel: the Schottky trio. Experiences of Extended X-ray Absorption Fine structure Spectroscopy (EXAFS) and X-ray Photoelectron Spectroscopy (XPS) on uranium dioxide doped by ionic implantation will help us in the comprehension of the studied phenomena and the interpretation of our calculations. (author). 256 refs.

  10. Analytical Characterization of the Thorium Nitrate Stockpile

    Energy Technology Data Exchange (ETDEWEB)

    Mattus, CH

    2003-12-30

    For several years, Oak Ridge National Laboratory (ORNL) has been supporting the Defense Logistics Agency-Defense National Stockpile Center with stewardship of a thorium nitrate (ThN) stockpile. The effort for fiscal year 2002 was to prepare a sampling and analysis plan and to use the activities developed in the plan to characterize the ThN stockpile. The sampling was performed in June and July 2002 by RWE NUKEM with oversight by ORNL personnel. The analysis was performed by Southwest Research Institute of San Antonio, Texas, and data validation was performed by NFT, Inc., of Oak Ridge, Tennessee. Of the {approx} 21,000 drums in the stockpile, 99 were sampled and 53 were analyzed for total metals composition, radiological constituents (using alpha and gamma spectrometry), and oxidizing characteristics. Each lot at the Curtis Bay Depot was sampled. Several of the samples were also analyzed for density. The average density of the domestic ThN was found to be 1.89 {+-} 0.08 g/cm{sup 3}. The oxidizer test was performed following procedures issued by the United Nations in 1999. Test results indicated that none of the samples tested was a Division 5.1 oxidizer per Department of Transportation definition. The samples were analyzed for total metals following the U.S. Environmental Protection Agency methods SW-846-6010B and 6020 (EPA 2003) using a combination of inductively coupled plasma--atomic emission spectroscopy and inductively coupled plasma--mass spectroscopy techniques. The results were used to compare the composition of the eight Resource Conservation and Recovery Act metals present in the sample (arsenic, barium, cadmium, chromium, lead, mercury, selenium, and silver) to regulatory limits. None of the samples was found to be hazardous for toxicity characteristics. The radiological analyses confirmed, when possible, the results obtained by the inductively coupled plasma analyses. These results--combined with the historical process knowledge acquired on the material

  11. Energy from thorium?! Reconnoitering a new possibility : FEA

    NARCIS (Netherlands)

    van Klinken, J.

    1998-01-01

    The worldwide increasing energy consumption depends largely on fossil resources and is not sustainable. Section 1 starts with a reflection on this precarious situation as an introduction to a recently proposed possibility of a thorium-fueled sub-critical reactor driven by a proton accelerator. In

  12. Structural phase transition and elastic properties of thorium pnictides ...

    Indian Academy of Sciences (India)

    In the present paper we have pointed out the weaknesses of the approach by Aynyas et al [1] to study the structural phase transition and elastic properties of thorium pnictides. The calculated values of phase transition pressure and other elastic properties using the realistic and actual approach are also given and compared ...

  13. Preparation of uranium compounds

    Science.gov (United States)

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

    2013-02-19

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

  14. METHOD OF ROLLING URANIUM

    Science.gov (United States)

    Smith, C.S.

    1959-08-01

    A method is described for rolling uranium metal at relatively low temperatures and under non-oxidizing conditions. The method involves the steps of heating the uranium to 200 deg C in an oil bath, withdrawing the uranium and permitting the oil to drain so that only a thin protective coating remains and rolling the oil coated uranium at a temperature of 200 deg C to give about a 15% reduction in thickness at each pass. The operation may be repeated to accomplish about a 90% reduction without edge cracking, checking or any appreciable increase in brittleness.

  15. CHEMICAL TOXICITY OF URANIUM

    Directory of Open Access Journals (Sweden)

    Sermin Cam

    2007-06-01

    Full Text Available Uranium, occurs naturally in the earth’s crust, is an alpha emitter radioactive element from the actinide group. For this reason, U-235 and U-238, are uranium isotopes with long half lives, have got radiological toxicity. But, for natural-isotopic-composition uranium (NatU, there is greater risk from chemical toxicity than radiological toxicity. When uranium is get into the body with anyway, also its chemical toxicity must be thought. [TAF Prev Med Bull 2007; 6(3.000: 215-220

  16. 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.

  17. Fission cross sections of some thorium, uranium, neptunium and plutonium isotopes relative to /sup 235/U

    Energy Technology Data Exchange (ETDEWEB)

    Meadows, J W

    1983-10-01

    Earlier results from the measurements, at this Laboratory, of the fission cross sections of /sup 230/Th, /sup 232/Th, /sup 233/U, /sup 234/U, /sup 236/U, /sup 238/U, /sup 237/Np, /sup 239/Pu, /sup 240/Pu, and /sup 242/Pu relative to /sup 235/U are reviewed with revisions to include changes in data processing procedures, alpha half lives and thermal fission cross sections. Some new data have also been included. The current experimental methods and procedures and the sample assay methods are described in detail and the sources of error are presented in a systematic manner. 38 references.

  18. Determination of uranium and thorium by neutron activation analysis applied to fossil samples dating

    Energy Technology Data Exchange (ETDEWEB)

    Ticianelli, Regina B.; Figueiredo, Ana Maria Graciano; Zahn, Guilherme S. [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Kinoshita, Angela; Baffa, Oswaldo [Universidade de Sao Paulo (FFCRLP/USP), Ribeirao Preto, SP (Brazil). Faculdade de Filosofia, Ciencias e Letras de Ribeirao Preto. Dept. de Fisica

    2011-07-01

    Electron Spin Resonance (ESR) dating is based on the fact that ionizing radiation can create stable free radicals in insulating materials, like tooth enamel and bones. The concentration of these radicals - determined by ESR - is a function of the dose deposed in the sample along the years. The accumulated dose of radiation, called Archaeological Dose, is produced by the exposition to environmental radiation provided by U, Th, K and cosmic rays. If the environmental dose rate in the site where the fossil sample is found is known, it is possible to convert this dose into the age of the sample. The annual dose rate coming from the radioactive elements present in the soil and in the sample itself can be calculated by determining the U, Th and K concentration. Therefore, the determination of the dose rate depends on the concentration of these main radioactive elements. Neutron Activation Analysis has the sensitivity and the accuracy necessary to determine U, Th and K with this objective. Depending on the composition of the sample, the determination of U and Th can be improved irradiating the sample inside a Cd capsule, reducing the thermal neutron incidence on the sample and, therefore, diminishing the activation of possible interfering nuclides. In this study the optimal irradiation and counting conditions were established for U and Th determination in fossil teeth and soil. (author)

  19. Adventures in Actinide Chemistry: A Year of Exploring Uranium and Thorium in Los Alamos

    Energy Technology Data Exchange (ETDEWEB)

    Pagano, Justin [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-01-08

    The first part of this collection of slides is concerned with considerations when working with actinides. The topics discussed in the document as a whole are the following: Actinide chemistry vs. transition metal chemistry--tools we can use; New synthetic methods to obtain actinide hydrides; Actinide metallacycles: synthesis, structure, and properties; and Reactivity of actinide metallacycles.

  20. (Uranium-Thorium)/Helium Thermochronologic Constraints on Secondary Iron-Oxide Mineralization in Southwestern New Mexico

    OpenAIRE

    Channer, Michael

    2017-01-01

    Southwestern New Mexico experienced protracted volcanism from ~60 Ma to 500 ka and associated epithermal mineralization. We apply hematite (U-Th)/He (hematite He) thermochronology to fracture-hosted hematite in the Lordsburg Mining District to resolve the timing of mineralization related to hydrothermal fluid circulation. We interpret hematite He dates with integrated field and structural observations, scanning electron microscopy to characterize hematite texture and grain size distribution, ...

  1. High pressure studies on uranium and thorium silicide compounds: Experiment and theory

    DEFF Research Database (Denmark)

    Yagoubi, S.; Heathman, S.; Svane, A.

    2013-01-01

    The actinide silicides ThSi, USi and USi2 have been studied under high pressure using both theory and experiment. High pressure synchrotron X-ray diffraction experiments were performed on polycrystalline samples in diamond anvil cells at room temperature and for pressures up to 54, 52 and 26 GPa,...

  2. Uranium and Thorium in Deep-Sea Manganese Nodules from the Central Pacific

    DEFF Research Database (Denmark)

    Kunzendorf, Helmar; Friedrich, G. H. W.

    1976-01-01

    When the analytical results of 119 ferromanganese samples were considered on a more regional basis, the authors found that U enrichment generally occurred in samples with relatively high Fe contents. For all areas together, the correlation between Fe and Th was a factor less than the correlation ...... in the shelf area, may indicate useful manganese nodules deposits in this area....

  3. Optical absorption spectra of the uranium (4+) ion in the thorium germanate matrix

    CERN Document Server

    Gajek, Z; Antic-Fidancev, E

    1997-01-01

    Visible and infrared absorption measurements on the U sup 4 sup + ion in tetragonal zircon-type matrix beta-ThGeO sub 4 are reported and analysed in terms of the standard parametrization scheme. The observed 17 main peaks and a number of less intense lines have been assigned and fitted to most of the 32 allowed electric dipole transitions with the root mean square error equal to 65 cm sup - sup 1. The free-ion parameters obtained for the model Hamiltonian, zeta 5f = 1809 cm sup - sup 1 , F sup 2 =43 065 cm sup - sup 1 , F sup 4 =38 977 cm sup - sup 1 and F sup 6 =24 391 cm sup - sup 1 , as well as the corresponding crystal-field parameters, B sub 0 sup 2 =-1790 cm sup - sup 1 , B sub 0 sup 4 =1200 cm sup - sup 1 , B sub 4 sup 4 =3260 cm sup - sup 1 , B sub 0 sup 6 =-3170 cm sup - sup 1 and B sub 4 sup 6 =990 cm sup - sup 1 , agree fairly well with the initial theoretical estimations. The results are discussed in relation to the previous spectroscopic study on the scheelite-type matrix UGeO sub 4. (author)

  4. Geochemistry of uranium and thorium and natural radioactivity levels of the western Anatolian plutons, Turkey

    Science.gov (United States)

    Papadopoulos, Argyrios; Altunkaynak, Şafak; Koroneos, Antonios; Ünal, Alp; Kamaci, Ömer

    2017-10-01

    Seventy samples from major plutons (mainly granitic) of Western Anatolia (Turkey) have been analyzed by γ-ray spectrometry to determine the specific activities of 238U, 226Ra, 232Th and 40K (Bq/kg). Τhe natural radioactivity ranged up to 264 Bq/kg for 238U, 229.62 Bq/kg for 226Ra, up to 207.32 Bq/kg for 232Th and up to 2541.95 Bq/kg for 40K. Any possible relationship between the specific activities of 226Ra, 238U, 232Th and 40K and some characteristics of the studied samples (age, rock-type, colour, grain size, occurrence, chemical and mineralogical composition) was investigated. Age, major and trace element geochemistry, color, pluton location and mineralogical composition are likely to affect the concentrations of the measured radionuclides. The range of the Th/U ratio was large (0.003-11.374). The latter, along with 226Ra/238U radioactive secular disequilibrium, is also discussed and explained by magmatic processes during differentiation.

  5. Age of the moon: An isotopic study of uranium-thorium-lead systematics of lunar samples

    Science.gov (United States)

    Tatsumoto, M.; Rosholt, J.N.

    1970-01-01

    Concentrations of U, Th, and Pb in Apollo 11 samples studied are low (U. 0.16 to 0.87; Th, 0.53 to 3.4; Pb, 0.29 to 1.7, in ppm) but the extremely radiogenic lead in samples allows radiometric dating. The fine dust and the breccia have a concordant age of 4.66 billion years on the basis of 207Pb/206Pb, 206Pb/238U, 207Pb/235U, and 208Pb/232Th ratios. This age is comparable with the age of meteorites and with the age generally accepted for the earth. Six crystalline and vesicular samples are distinctly younger than the dust and breccia. The 238U/235U ratio is the same as that in earth rocks, and 234U is in radioactive equilibrium with parent 238U.

  6. A comparative study of europium, thorium and uranium binding to an aquatic fulvic acid

    Energy Technology Data Exchange (ETDEWEB)

    Norden, M.; Ephraim, H.J.; Allard, B. [Linkoeping Univ. (Sweden); Albinsson, Y. [Chalmers Univ. of Technology, Goeteborg (Sweden)

    1993-12-31

    Advances in safe management and disposal of radioactive waste have shown that a comprehensive program requires the incorporation of dissolved organics into radwaste and transport effluent models, with respect to their binding of radionuclides. The binding of Eu{sup 3+}, Th{sup 4+} and UO{sub 2}{sup 2+} to a well-characterized aquatic fulvic acid has been studied using an ultrafiltration method at a bulk electrolyte concentration of 0.10 M NaClO{sub 4}, trace amounts of radionuclides and fulvic acid concentrations of 60 and 120 mg/l. The results expressed as the overall complex formation function, {beta}{sub ov}, versus pH show the following order: Th{sup 4+} > Eu{sup 3+} > UO{sub 2}{sup 2+}. The estimated {beta}{sub 0v} values have been discussed by considering the aqueous chemistry of Eu{sup 3+}, Th{sup 4+} and UO{sub 2}{sup 2+} vis-a-vis the solution chemistry of the fulvic acid sample.

  7. Complexation studies of uranium and thorium with a natural fulvic acid

    Energy Technology Data Exchange (ETDEWEB)

    Davis, J.R.; Higgo, J.J.W.; Noy, D.J.; Hooker, P.J. [British Geological Survey, Keyworth (United Kingdom)

    2000-10-01

    The BGS investigations under task 2 focussed on laboratory experiments to elucidate the complexation behaviour of aqueous U(VI) and Th(IV) with a well-characterised natural fulvic acid, DE72 FA, collected from the Derwent Reservoir, Derbyshire, UK. This paper summarises the previous BGS work on U and Th complexation and describes some new results for Th dissociation. Three laboratory batch methods, involving ion-exchange, solvent extraction and kinetics experiments, were used to study the complexation behaviour of U and Th with DE72FA covering a range of ionic strengths and pH. The ion exchange and solvent extraction experiments gave similar conditional stability constant results for U, and the log beta values were of the same order as those obtained previously for other U-natural fulvic acid systems. Batch kinetics experiments were used to measure the rates of dissociation of U and Th from their complexes with DE72 FA. The calculated rate constants were reciprocated to give the average-lives or time-constants ({tau}1, {tau}2 and {tau}3) of the metals in the three binding modes. The {tau}3 times for Th undergoing slow dissociation ranged from 470 to 1913 hours and were much less sensitive to metal-fulvic acid equilibration time and ionic strength than the {tau}3 values for U. The slow dissociation rates for U were comparable to the Th rates after the longest period of U-fulvic acid equilibration, but the fraction of U remaining in the hindered sites was much smaller ({proportional_to}7% compared to {proportional_to}55% for Th). Although it was not possible to determine the irreversibly-bound proportions of these fractions of U and Th in the hindered sites, these new data serve as important constraints when modelling the far-field transport of actinide-fulvate complexes under in-situ conditions. (orig.)

  8. Uranium and thorium series nuclides in river sediments and river water

    Energy Technology Data Exchange (ETDEWEB)

    Scott, M. R.; Salter, P. F

    1980-01-01

    Large volume suspended sediment samples were taken from Rio Grande, Mississippi and Suwannee Rivers. These rivers drain arid, moderate and subtropical regions, respectively. The samples were taken to provide enough material to use for chemical fractionation leaching studies of the relationship between Pu and other nuclides with various components of the sediment. This work is still in progress and is described in detail in a separate section of the progress report.

  9. Humic acid provenance influence to the adsorption capacity in uranium and thorium removal

    Science.gov (United States)

    Prasetyo, E.

    2018-01-01

    It is common knowledge that humic acid is organic compound without certain chemical composition since it is derived from different organic materials. Further this raises question whether the different humic acid sample used could lead to different adsorbent properties e.g. adsorption capacity. To address the problem, this paper is aimed to clarify the relation between the provenances of humic acid and synthesized adsorbent properties especially adsorption capacities by quantitative and qualitative functional groups determination including discussion on their effect to the metal ion adsorption mechanism using three humic acid samples. Two commercial samples were derived from recent compost while the other extracted from tertiary carbonaceous mudstone strata.

  10. Uranium industry annual 1993

    Energy Technology Data Exchange (ETDEWEB)

    1994-09-01

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

  11. 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

    This document brings together the abstracts of the 39 presentations given at this meeting days on uranium, organized by the French geological society, and dealing with: 1 - Prospective study of the electronuclear technological transition; 2 - The front-end of the nuclear cycle: from the molecule to the process; 3 - Geophysics: recent changes; 4 - Use of well logging in uranium exploration; 5 - Genetical classification of thorium deposits; 6 - Genetical nomenclature of uranium sources; 7 - Uranium deposits linked to a Proterozoic discordance - retrospective; 8 - The use of spectral analysis techniques in uranium exploration: real-time mapping of clay alteration features; 9 - Development of functionalized silk-screened carbon electrodes for the analysis of uranium trace amounts; 10 - Study of the actinides solvation sphere in organic environment; 11 - Thermodynamic of uraniferous phases of interest for the nuclear cycle; 12 - Heap leaching of marginal minerals at Somair: from lab studies to the production of 700 t of uranium/year; 13 - Agglomeration phenomenology and role of iron in uranium heap leaching; 14 - Chloride uranyl complexes up to 300 deg. C along the saturation vapour curve: Raman spectroscopy analysis and metallogenic consequences; 15 - Weathering systems in the Shea Creek deposit (Athabasca, Canada): vertical variability of argillaceous weathering; 16 - Weathering systems in the Shea Creek deposit (Athabasca, Canada): contribution of irradiation defects in clays to the tracing of past uranium migrations; 17 - Uranium concentrations in mineralizing fluids of the Athabasca basin: analytical and experimental approach; 18 - Paleo-surfaces and metallic rooting: the autochthonous uranium of pre-Athabasca paleo-alterites, Canada; 19 - Distribution of argillaceous parageneses in the Imouraren deposit - Niger; 20 - Heat flux and radioelements concentration (U, Th, K) of precambrian basements: implications in terms of crust growth mechanisms, paleo

  12. Uranium: A Dentist's perspective.

    Science.gov (United States)

    Toor, R S S; Brar, G S

    2012-01-01

    Uranium is a naturally occurring radionuclide found in granite and other mineral deposits. In its natural state, it consists of three isotopes (U-234, U-235 and U-238). On an average, 1% - 2% of ingested uranium is absorbed in the gastrointestinal tract in adults. The absorbed uranium rapidly enters the bloodstream and forms a diffusible ionic uranyl hydrogen carbonate complex (UO2HCO3+) which is in equilibrium with a nondiffusible uranyl albumin complex. In the skeleton, the uranyl ion replaces calcium in the hydroxyapatite complex of the bone crystal. Although in North India, there is a risk of radiological toxicity from orally ingested natural uranium, the principal health effects are chemical toxicity. The skeleton and kidney are the primary sites of uranium accumulation. Acute high dose of uranyl nitrate delays tooth eruption, and mandibular growth and development, probably due to its effect on target cells. Based on all previous research and recommendations, the role of a dentist is to educate the masses about the adverse effects of uranium on the overall as well as the dental health. The authors recommended that apart from the discontinuation of the addition of uranium to porcelain, the Public community water supplies must also comply with the Environmental Protection Agency (EPA) standards of uranium levels being not more than 30 ppb (parts per billion).

  13. Incorporation of tetravalent actinides in three phosphated matrices: britholite, monazite/brabandite and thorium phosphate diphosphate ({beta}-TPD); Incorporation d'actinides tetravalents dans trois matrices phosphatees: britholite, monazite/brabantite et phosphate - diphosphate de thorium ({beta}-PDT)

    Energy Technology Data Exchange (ETDEWEB)

    Terra, O

    2005-03-01

    Three phosphate based ceramics were studied for the immobilization of tri- and tetravalent actinides: britholite Ca{sub 9}Nd{sub 1-x}An{sub x}{sup IV}(PO{sub 4}){sub 5-x}(SiO{sub 4}){sub 1+x}F{sub 2}, monazite/brabantite solid solutions Ln{sub 1-2x}{sup III} Ca{sub x}An{sub x}{sup IP}O{sub 4} and Thorium Phosphate Diphosphate ({beta}-TPD) Th{sub 4-}xAn{sub x}{sup IV}(PO{sub 4}){sub 4}P{sub 2}O{sub 7}. For each material, the incorporation of thorium and uranium (IV) was studied as a surrogate of plutonium. This work was the early beginning of the incorporation of {sup 239}Pu and/or {sup 238}Pu in order to evaluate the effects of {alpha}-decay on the three crystallographic structures. The incorporation of tetravalent cations was carried out by dry chemistry methods, using mechanical grinding to improve the reactivity of the initial mixture then the homogeneity of final solid prepared after calcination at high temperature (1200-1400 deg C). For britholites, the thorium incorporation was complete for weight loading up to 20 wt.%, leading to the preparation of homogeneous and single phase solid solutions when using the coupled substitution (Nd{sup 3+}, PO{sub 4}{sup 3-}) {r_reversible} (Th{sup 4+}, SiO{sub 4}{sup 4-}). Due to redox problems, the incorporation of uranium was limited to 5 to 8 wt.% and always led to a two-phase mixture of U-britholite and CaU{sub 2}O{sub 5+y}. The preparation of homogeneous solid solutions of {beta}-TUPD and of brabantites containing thorium and uranium samples was successfully obtained using three steps of mechanical grinding/calcination. For each matrix, dense pellets were prepared prior to the study of their chemical behaviour during leaching tests. The chemical durability of brabantites and {beta}-TUPD were found to be close to that reported in literature. The formation of neo-formed phases was also evidenced onto the surface of Th-britholite samples. (author)

  14. Uranium dioxide electrolysis

    Science.gov (United States)

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

    2009-12-29

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

  15. Mobility of radium and uranium in an uranium mill tailings deposit; Mobilite du radium et de l`uranium dans un site de stockage de residus issus du traitement de minerais d`uranium

    Energy Technology Data Exchange (ETDEWEB)

    Bassot, S. [CEA Centre d`Etudes de Fontenay-aux-Roses, 92 (France). Dept. de Protection de l`Environnement et des Installations]|[Besancon Univ., 25 (France)

    1997-03-01

    In France, the extraction of uranium for nuclear power plants has generated more than 60 millions tons of residues. They are disposed at the surface and contain still more than 70 % of the initial activity of the ores due to the presence of uranium 238 daughters like thorium 230, radium 226 and lead 210. When water percolates through the tailings, the radioelements can migrate until they reach the geosphere. The radioelements rate coming from such a disposal depends on the hydrodynamic characteristics of the site and on the physicochemical processes which control the mobility of the radioelements. Therefore, we have studied the geochemical behaviour of radium and uranium at the Lengenfeld site in Germany. Analysis of the residues has allowed us to reconstituted the history of the site. The disposal was probably the result of an alkaline treatment applied to a mixture of granitic and sedimentary ores. Moreover, this analysis has permitted us to determine the nature of the mineral phases which can sorb the radioelements (clays, carbonate phases and iron oxo-hydroxides). For some of them, a mechanism of sorption was proposed and the associated constants were determined. Applying geochemical codes to our results has shown which solids control the solution composition and has also permitted us to estimate the distribution of radium between the solid and solution phases. From these data, the beginning of a prediction of the radium mobility evolution with time, at the Lengenfeld site, has been carried out. (authors) 50 refs.

  16. Utilisation of mixer-settler on thorium purification from raw thorium hydroxide; Uso de um misturador-decantador na purificacao de torio proveniente do hidroxido de torio bruto

    Energy Technology Data Exchange (ETDEWEB)

    Gomes, Luciano F.; Carvalho, Fatima M.S.; Mindrisz, Ana C.; Scapin, Marcos A.; Salvador, Vera R.L.; Lainetti, Paulo E.O. [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil). Centro de Quimica e Meio Ambiente

    2002-07-01

    In this paper one showed the development of a process for the obtainment of pure thorium nitrate from a thorium concentrate known as raw thorium hydroxide (HTBR). This concentrate is mainly constituted by thorium hydroxides, rare earths, iron, lead, calcium and silica among other impurities. After several experiments and analyses through wet analytical chemical methods and X-Ray fluorescence the operation conditions were optimized. The process includes the dissolution of HTBR in nitric medium and flocculation for the separation of the insoluble ones until the final purification by solvent extraction. In this stage a mixer-settler unit with tri-n-butil phosphate eextractor agent was utilized. At end of the process a thorium nitrate with a high purity degree and a rich concentrate of rare earths were obtained which will be later purified were obtained. (author)

  17. Accident analysis of heavy water cooled thorium breeder reactor

    Science.gov (United States)

    Yulianti, Yanti; Su'ud, Zaki; Takaki, Naoyuki

    2015-04-01

    Thorium has lately attracted considerable attention because it is accumulating as a by-product of large scale rare earth mining. The objective of research is to analyze transient behavior of a heavy water cooled thorium breeder that is designed by Tokai University and Tokyo Institute of Technology. That is oxide fueled, PWR type reactor with heavy water as primary coolant. An example of the optimized core has relatively small moderator to fuel volume ratio (MFR) of 0.6 and the characteristics of the core are burn-up of 67 GWd/t, breeding ratio of 1.08, burn-up reactivity loss during cycles of fuel and claddings during accident are still below limitations which are in secure condition.

  18. Point defects in thorium nitride: A first-principles study

    Energy Technology Data Exchange (ETDEWEB)

    Pérez Daroca, D., E-mail: pdaroca@tandar.cnea.gov.ar [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas (Argentina); Llois, A.M. [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas (Argentina); Mosca, H.O. [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica (Argentina); Instituto de Tecnología Jorge A. Sabato, UNSAM-CNEA (Argentina)

    2016-11-15

    Thorium and its compounds (carbides and nitrides) are being investigated as possible materials to be used as nuclear fuels for Generation-IV reactors. As a first step in the research of these materials under irradiation, we study the formation energies and stability of point defects in thorium nitride by means of first-principles calculations within the framework of density functional theory. We focus on vacancies, interstitials, Frenkel pairs and Schottky defects. We found that N and Th vacancies have almost the same formation energy and that the most energetically favorable defects of all studied in this work are N interstitials. These kind of results for ThN, to the best authors' knowledge, have not been obtained previously, neither experimentally, nor theoretically.

  19. First-principles study of point defects in thorium carbide

    Energy Technology Data Exchange (ETDEWEB)

    Pérez Daroca, D., E-mail: pdaroca@tandar.cnea.gov.ar [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica, Av. General Paz 1499, (1650) San Martin, Buenos Aires (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas, (1033) Buenos Aires (Argentina); Jaroszewicz, S. [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica, Av. General Paz 1499, (1650) San Martin, Buenos Aires (Argentina); Instituto de Tecnología Jorge A. Sabato, UNSAM-CNEA, Av. General Paz 1499, (1650) San Martin, Buenos Aires (Argentina); Llois, A.M. [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica, Av. General Paz 1499, (1650) San Martin, Buenos Aires (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas, (1033) Buenos Aires (Argentina); Mosca, H.O. [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica, Av. General Paz 1499, (1650) San Martin, Buenos Aires (Argentina); Instituto de Tecnología Jorge A. Sabato, UNSAM-CNEA, Av. General Paz 1499, (1650) San Martin, Buenos Aires (Argentina)

    2014-11-15

    Thorium-based materials are currently being investigated in relation with their potential utilization in Generation-IV reactors as nuclear fuels. One of the most important issues to be studied is their behavior under irradiation. A first approach to this goal is the study of point defects. By means of first-principles calculations within the framework of density functional theory, we study the stability and formation energies of vacancies, interstitials and Frenkel pairs in thorium carbide. We find that C isolated vacancies are the most likely defects, while C interstitials are energetically favored as compared to Th ones. These kind of results for ThC, to the best authors’ knowledge, have not been obtained previously, neither experimentally, nor theoretically. For this reason, we compare with results on other compounds with the same NaCl-type structure.

  20. {sup 232}Th/{sup 238}U in a uranium mobility estimate in an agricultural area in the municipality of Pedra-Pernambuco - Brazil

    Energy Technology Data Exchange (ETDEWEB)

    Santos Junior, Jose Araujo dos; Amaral, Romilton dos Santos; Bezerra, Jairo Dias; Damascena, Kennedy Francys Rodrigues; Oliveira, Jose Valdez Monterazo de; Bispo, Rodrigo Cesar Bezerra, E-mail: jaraujo@ufpe.br [Departamento de Energia Nuclear - Grupo de Radioecologia (RAE). Universidade Federal de Pernambuco (UFPE), Recife, PE (Brazil); Silva, Cleomacio Miguel da [Universidade de Pernambuco (UPE), Petrolina, PE (Brazil). Departamento de Matematica; Rocha, Edilson Accioly [Instituto Federal de Educacao, Ciencia e Tecnologia de Pernambuco, Recife, PE (Brazil). Departamento de Quimica

    2011-07-01

    The mobility of the radionuclides in soil depends primarily on the physic-chemical parameters. The uranium is easily oxidized in aqueous environment, which allows its characterization with higher mobility. The Thorium is practically insoluble, mainly if the environment has organic matter and sulfates. The geochemical characteristics of the rocks, associated with the weather and metamorphism produce alterations in the concentration diagrams of the natural radionuclides in different types of soil. The ratio {sup 232}Th/{sup 238}U has been used as an indicator of oxidizing and reducing conditions. Th/U less than 2 suggests that the uranium is in its concentrated form abundantly when compared to the thorium. In reducing conditions, the value Th/U higher than 7 indicates a removal of the uranium. In this work it was possible to analyze the agricultural soil in the municipality of Pedra, Pernambuco, Brazil where there are uranium anomaly and thorium in rocky outcrops. Sixty-two samples of the horizon C soil were collected, in an area of 2 km{sup 2}, where the main uranium occurrences are located. The analyses were done by High-Resolution Gamma-Spectroscopy. In the analyses the secular equilibrium was assumed and the {sup 238}U and the {sup 232}Th specific activities were used to estimate the oxidizing and reducing conditions defining the uranium mobility in the soil. The obtained findings show that the ratio Th/U varied from 0.3 to 13.4, with average of 4.6. The biggest {sup 238}U fraction was fix (80.3%), with low mobility; the smallest fraction concentrated (6.6%) and a lixiviated intermediate fraction (13.1%). (author)

  1. Phonon spectrum, mechanical and thermophysical properties of thorium carbide

    Energy Technology Data Exchange (ETDEWEB)

    Pérez Daroca, D., E-mail: pdaroca@tandar.cnea.gov.ar [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica (Argentina); Consejo Nacional de Investigaciones Cientı´ficas y Técnicas (Argentina); Jaroszewicz, S. [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica (Argentina); Instituto de Tecnología Jorge A. Sabato, UNSAM-CNEA (Argentina); Llois, A.M. [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica (Argentina); Consejo Nacional de Investigaciones Cientı´ficas y Técnicas (Argentina); Mosca, H.O. [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica (Argentina); Instituto de Tecnología Jorge A. Sabato, UNSAM-CNEA (Argentina)

    2013-06-15

    In this work, we study, by means of density functional perturbation theory and the pseudopotential method, mechanical and thermophysical properties of thorium carbide. These properties are derived from the lattice dynamics in the quasi-harmonic approximation. The phonon spectrum of ThC presented in this article, to the best authors’ knowledge, have not been studied, neither experimentally, nor theoretically. We compare mechanical properties, volume thermal expansion and molar specific capacities with previous results and find a very good agreement.

  2. On the structure of thorium and americium adenosine triphosphate complexes.

    Science.gov (United States)

    Mostapha, Sarah; Fontaine-Vive, Fabien; Berthon, Laurence; Boubals, Nathalie; Zorz, Nicole; Solari, Pier Lorenzo; Charbonnel, Marie Christine; Den Auwer, Christophe

    2014-11-01

    The actinides are chemical poisons and radiological hazards. One challenge to better appraise their toxicity and develop countermeasures in case of exposure of living organisms is to better assess pathways of contamination. Because of the high chemical affinity of those actinide elements for phosphate groups and the ubiquity of such chemical functions in biochemistry, nucleotides and in particular adenosine triphosphate nucleotide (ATP) may be considered critical target building blocks for actinides. Combinations of spectroscopic techniques (Fourier transformed Infra Red [FTIR], Electrospray Ionization Mass Spectrometry [ESI-MS], and Extended X-ray Absorption Fine Structure [EXAFS]) with quantum chemical calculations have been implemented in order to assess the actinides coordination arrangement with ATP. We describe and compare herein the interaction of ATP with thorium and americium; thorium(IV) as a representative of actinide(IV) like plutonium(IV) and americium(III) as a representative of all heavier actinides. In the case of thorium, an insoluble complex is readily formed. In the case of americium, a behavior identical to that described previously for lutetium has been observed with insoluble and soluble complexes. The comparative study of ATP complexation with Th(IV) and Am(III) shows their ability to form insoluble complexes for which a structural model has been proposed by analogy with previously described Lu(III) complexes.

  3. UDATE1: A computer program for the calculation of uranium-series isotopic ages

    Science.gov (United States)

    Rosenbauer, Robert J.

    UDATE1 is a FORTRAN-77 program with an interface for an Apple Macintosh computer that calculates isotope activities from measured count rates to date geologic materials by uranium-series disequilibria. Dates on pure samples can be determined directly by the accumulation of 230Th from 234U and of 231Pa from 235U. Dates for samples contaminated by clays containing abundant natural thorium can be corrected by the program using various mixing models. Input to the program and file management are made simple and user friendly by a series of Macintosh modal dialog boxes.

  4. Uranium hydrogeochemical and stream sediment reconnaissance data release for the Elk City NTMS Quadrangle, Idaho/Montana, including concentrations of forty-five additional elements

    Energy Technology Data Exchange (ETDEWEB)

    Broxton, D.E.; Beyth, M.

    1980-07-01

    Totals of 1580 water and 1720 sediment samples were collected from 1754 locations in the quadrangle. Elemental concentration, field measurement, weather, geologic, and geographic data for each sample location are listed for waters in Appendix I-A and for sediments in Appendix I-B. Uranium/thorium ratios for sediment samples are also included in Appendix I-B. All elemental analyses were performed at the LASL. Water samples were initially analyzed for uranium by fluorometry. All water samples containing more than 40 parts per billion (ppB) uranium were reanalyzed by delayed-neutron counting (DNC). A supplemental report containing the multielement analyses of water samples will be open filed in the near future. Sediments were analyzed for uranium and thorium as well as aluminum, antimony, arsenic, barium, beryllium, bismuth, cadmium, calcium, cerium, cesium, chlorine, chromium, cobalt, copper, dysprosium, europium, gold, hafnium, iron, lanthanum, lead, lithium, lutetium, magnesium, manganese, nickel, niobium, potassium, rubidium, samarium, selenium, scandium, silver, sodium, strontium, tantalum, terbium, tin, titanium, tungsten, vanadium, ytterbium, zinc, and zirconium. Basic statistics for 40 of these elements are presented. All sediments were analyzed for uranium by delayed-neutron counting. Other elemental concentrations in sediments were determined by neutron-activation analysis for 30 elements, by x-ray fluorescence for 12 elements, and by arc-source emission spectrography for 2 elements. Analytical results for sediments are reported as parts per million.

  5. Production of Actinium-225 via High Energy Proton Induced Spallation of Thorium-232

    Energy Technology Data Exchange (ETDEWEB)

    Harvey, James T.; Nolen, Jerry; Vandergrift, George; Gomes, Itacil; Kroc, Tom; Horwitz, Phil; McAlister, Dan; Bowers, Del; Sullivan, Vivian; Greene, John

    2011-12-30

    The science of cancer research is currently expanding its use of alpha particle emitting radioisotopes. Coupled with the discovery and proliferation of molecular species that seek out and attach to tumors, new therapy and diagnostics are being developed to enhance the treatment of cancer and other diseases. This latest technology is commonly referred to as Alpha Immunotherapy (AIT). Actinium-225/Bismuth-213 is a parent/daughter alpha-emitting radioisotope pair that is highly sought after because of the potential for treating numerous diseases and its ability to be chemically compatible with many known and widely used carrier molecules (such as monoclonal antibodies and proteins/peptides). Unfortunately, the worldwide supply of actinium-225 is limited to about 1,000mCi annually and most of that is currently spoken for, thus limiting the ability of this radioisotope pair to enter into research and subsequently clinical trials. The route proposed herein utilizes high energy protons to produce actinium-225 via spallation of a thorium-232 target. As part of previous R and D efforts carried out at Argonne National Laboratory recently in support of the proposed US FRIB facility, it was shown that a very effective production mechanism for actinium-225 is spallation of thorium-232 by high energy proton beams. The base-line simulation for the production rate of actinium-225 by this reaction mechanism is 8E12 atoms per second at 200 MeV proton beam energy with 50 g/cm2 thorium target and 100 kW beam power. An irradiation of one actinium-225 half-life (10 days) produces {approx}100 Ci of actinium-225. For a given beam current the reaction cross section increases slightly with energy to about 400 MeV and then decreases slightly for beam energies in the several GeV regime. The object of this effort is to refine the simulations at proton beam energies of 400 MeV and above up to about 8 GeV. Once completed, the simulations will be experimentally verified using 400 MeV and 8 Ge

  6. Study of the uranium availability through the research method Th/U

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez, Zahily Herrero; Santos Junior, Jose Araujo dos; Amaral, Romilton dos Santos; Santos, Josineide Marques do Nascimento; Damascena, Kennedy Francys Rodrigues; Medeiros, Nilson Vicente da Silva; Maciel Neto, Jose de Almeida, E-mail: zahily1985@gmail.com, E-mail: jaraujo@ufpe.br, E-mail: romilton@ufpe.br, E-mail: neideden@hotmail.com, E-mail: kennedy.eng.ambiental@gmail.com, E-mail: nvsmedeiros@gmail.com, E-mail: profjosemaciel@gmail.com [Universidade Federal de Pernambuco (UFPE), Recife, PE (Brazil). Centro de Tecnologia e Geociencias. Departamento de Energia Nuclear; Alvarez, Juan Reinaldo Estevez, E-mail: jestevez@ceaden.cu [Centro de Aplicaciones Tecnologicas y Desarrollo Nuclear (CEADEN), Havana (Cuba); Silva, Alberto Antonio da, E-mail: alberto.silva@barreiros.ifpe.edu.br [Instituto Federal de Educacao, Ciencia e Tecnologia de Pernambuco (IFPE), Barreiros, PE (Brazil)

    2015-07-01

    The uranium and thorium, precursors of the main natural radioactive series, have different concentrations in the Earth's crust. The ratio Th/U has been used as an indicator of oxidizing and reducing conditions, whose factors suggest availability of uranium to displacement in the environment and incorporations in different matrices. This parameter become essential to determine possible conditions of availability by the chemical form and incorporation in the food chain. The state of Paraiba, in northeastern Brazil, has a uranium deposits located in Sao Jose de Espinharas, where there are agricultural practices in areas surrounding the deposit of natural uranium. The Environmental Monitoring Program and Radioecological, making it an area that offers all the features for research mobility of uranium, chemical form and availability of incorporation, in addition to understanding the kinetics and transport of this natural radionuclide in the environment. Soil samples were collected from agricultural areas, close to the uraniferous occurrences where the samples were analyzed in the Laboratorio de Radioecologia e Controle Ambiental (LARCA) of the Departamento de Energia Nuclear at the Universidade Federal de Pernambuco (UFPE) by High Resolution Gamma Spectrometry, obtaining the experimental activities of {sup 238}U and {sup 232}Th using indirect gamma measures. The obtained findings show that the ratio Th/U varied from 0.11 to 1.33, with an average of 0.69. (author)

  7. Uranium Location Database

    Data.gov (United States)

    U.S. Environmental Protection Agency — A GIS compiled locational database in Microsoft Access of ~15,000 mines with uranium occurrence or production, primarily in the western United States. The metadata...

  8. Uranium hexakisamido complexes

    Energy Technology Data Exchange (ETDEWEB)

    Meyer, K.; Mindiola, D.J.; Baker, T.A.; Davis, W.M.; Cummins, C.C. [Massachusetts Inst. of Tech., Cambridge, MA (United States). Dept. of Chemistry

    2000-09-01

    Minimal structural changes accompany the oxidation of the paramagnetic uranium(V) anion [U(dbabh){sub 6}]{sup -} to the neutral, diamagnetic counterpart [U(dbabh){sub 6}] (see structure). These two T{sub h}-stmmetric complexes, which were synthetized starting from 2,3:5,6-dibenzo-7-azabicyclo[2.2.1]hepta-2,5-diene (Hdbabh), are the first isolable homoleptic hexakisamido complexes of uranium(V) and (VI). (orig.)

  9. Accumulation of uranium by biopigments

    Energy Technology Data Exchange (ETDEWEB)

    Sakaguchi, Takashi; Nakajima, Akira

    1987-01-01

    The uranium adsorbing abilities of various biopigments were investigated. Extremely high adsorption capacities for uranium were found in melanin and bioflavonols (quercetin and morin) having chelating positions with uranium. As a step towards improving the adsorption characteristics of the bioflavonols, quercetin and morin were immobilized on both Bemberg rayon fiber and polyaminostyrene, and the basic features of uranium adsorption by the immobilized bioflavonols were studied. The bioflavonols immobilized on Bemberg rayon fiber have a highly selective capacity to adsorb uranium. Uranium recovery from seawater by the immobilized bioflavonols was markedly affected by the pH value of the seawater, and the uptake at pH 8, which is the pH value of natural seawater, was difficult. However, this adsorbent can accumulate large amounts of uranium from non-saline water. Thus it can be used to remove and recover uranium from uranium refining waste water and other waste sources.

  10. 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

  11. Operation of CANDU power reactor in thorium self-sufficient fuel cycle

    Indian Academy of Sciences (India)

    This paper presents the results of calculations for CANDU reactor operation in thorium fuel cycle. Calculations are performed to estimate the feasibility of operation of heavy-water thermal neutron power reactor in self-sufficient thorium cycle. Parameters of active core and scheme of fuel reloading were considered to be the ...

  12. New twists and turns for actinide chemistry. Organometallic infinite coordination polymers of thorium diazide

    Energy Technology Data Exchange (ETDEWEB)

    Monreal, Marisa J.; Seaman, Lani A.; Goff, George S.; Michalczyk, Ryszard; Morris, David E.; Scott, Brian L.; Kiplinger, Jaqueline L. [Los Alamos National Laboratory, Los Alamos, NM (United States)

    2016-03-07

    Two organometallic 1D infinite coordination polymers and two organometallic monometallic complexes of thorium diazide have been synthesized and characterized. Steric control of these self-assembled arrays, which are dense in thorium and nitrogen, has also been demonstrated: infinite chains can be circumvented by using steric bulk either at the metallocene or with a donor ligand in the wedge.

  13. Design of a homogeneous subcritical nuclear reactor based on thorium with a source of californium 252; Diseno de un reactor nuclear subcritico homogeneo a base de Torio con una fuente de Californio 252

    Energy Technology Data Exchange (ETDEWEB)

    Delgado H, C. E.; Vega C, H. R. [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Cipres No. 10, Fracc. La Penuela, 98068 Zacatecas, Zac. (Mexico); Sajo B, L., E-mail: ce_delgado89@hotmail.com [Universidad Simon Bolivar, Laboratorio de Fisica Nuclear, Apdo. 89000, 1080A Caracas (Venezuela, Bolivarian Republic of)

    2015-10-15

    Full text: One of the energy alternatives to fossil fuels which do not produce greenhouse gases is the nuclear energy. One of the drawbacks of this alternative is the generation of radioactive wastes of long half-life and its relation to the generation of nuclear materials to produce weapons of mass destruction. An option to these drawbacks of nuclear energy is to use Thorium as part of the nuclear fuel which it becomes in U{sup 233} when capturing neutrons, that is a fissile material. In this paper Monte Carlo methods were used to design a homogeneous subcritical reactor based on thorium. As neutron reflector graphite was used. The reactor core is homogeneous and is formed of 70% light water as moderator, 12% of enriched uranium UO{sub 2}(NO{sub 3}){sub 4} and 18% of thorium Th(NO{sub 3}){sub 4} as fuel. To start the nuclear fission chain reaction an isotopic source of californium 252 was used with an intensity of 4.6 x 10{sup 7} s{sup -1}. In the design the value of the effective multiplication factor, whose value turned out k{sub eff} <1 was calculated. Also, the neutron spectra at different distances from the source and the total fluence were calculated, as well as the values of the ambient dose equivalent in the periphery of the reactor. (Author)

  14. Thorium Chemistry in Oxo-Tellurium System under Extreme Conditions.

    Science.gov (United States)

    Xiao, Bin; Kegler, Philip; Bosbach, Dirk; Alekseev, Evgeny V

    2017-03-06

    Through the use of a high-temperature/high-pressure synthesis method, four thorium oxo-tellurium compounds with different tellurium valence states were isolated. The novel inorganic phases illustrate the intrinsic complexity of the actinide tellurium chemistry under extreme conditions of pressure and temperature. Th2Te3O11 is the first instance of a mixed-valent oxo-tellurium compound, and at the same time, Te exhibits three different coordination environments (TeIVO3, TeIVO4, and TeVIO6) within a single structure. These three types of Te polyhedra are further fused together, resulting in a [Te3O11]8- fragment. Na4Th2(TeVI3O15) and K2Th(TeVIO4)3 are the first alkaline thorium tellurates described in the literature. Both compounds are constructed from ThO9 tricapped trigonal prisms and TeVIO6 octahedra. Na4Th2(TeVI3O15) is a three-dimensional framework based on Th2O15 and Te2O10 dimers, while K2Th(TeVIO4)3 contains tungsten oxide bronze like Te layers linked by ThO9 polyhedra. The structure of β-Th(TeIVO3)(SO4) is built from infinite thorium chains cross-linked by TeIVO32- and SO42- anions. Close structural analysis suggests that β-Th(TeIVO3)(SO4) is highly related to the structure of α-Th(SeO4)2. Additionally, the Raman spectra are recorded and the characteristic peaks are assigned based on a comparison of reported tellurites or tellurates.

  15. Ecological condition around the uranium tailing pits in Tajikistan

    Energy Technology Data Exchange (ETDEWEB)

    Mirsaidov, I.; Mirsaidov, U.; Khakimov, N.; Nazarov, Kh. [Nuclear and Radiation Safety Agency under the Academy of Sciences of the Republic of Tajikistan, 33 Rudaki avenue, Dushanbe 734025 (Tajikistan)

    2010-07-01

    One of the basic sectors of the economy in Tajikistan is the mining industry. Its development in the past led to an accumulation of large amounts of waste mainly associated with the uranium milling facilities. These wastes contain radionuclides in high concentrations (basically uranium- thorium series) and other hazardous substances. These facilities are often located in residential areas and in the upper side of the main watersheds of the region, such as Amu-Daria and Syr-Daria. Tajikistan has a number of uranium ore deposits and mining and milling facilities, which operated in the past. This country's own ores and imported raw materials were processed mainly at the former Leninabad Geochemical Combine facility (currently State Enterprise (SE) 'Vostokredmet') and also at other hydro-metallurgical plants located in the vicinity of uranium ore extraction sites (Adrasman, Taboshar, Isphara etc.). Presently the only operating enterprise in the Republic of Tajikistan, which still has the potential to process Uranium ores, using an acid leach extraction process, is the SE 'Vostokredmet'. It is interesting is to note that the mine wastes at the Adrasman site were recently successfully reprocessed to produce a lead concentrate. Otherwise, all underground and open pit mines and old radium and uranium facilities have been decommissioned, but most of them are still not remediated. Due to the recent significant increase in the price of uranium, the uranium mining residues have become a focus of interest for various different investors and commercial companies who are considering reprocessing the waste rock piles and mill tailings of Northern Tajikistan. Based on estimates from SE 'Vostokredmet', the total amount of residual uranium in the tailings and waste rock piles in the Republic of Tajikistan is about 55 million tons. The total activity of these wastes is estimated to be approximately 240-285 10{sup 12} Bq. The total volume of waste

  16. Uranium: War, Energy and the Rock That Shaped the World; Uranium: la biographie

    Energy Technology Data Exchange (ETDEWEB)

    Zoellner, T.

    2009-07-01

    Having traveled extensively through the savannah of Africa, the mountains of Eastern Europe, and the deserts of Utah, the author delves into the complex science, politics and history of uranium, which presents the best and worst of mankind: the capacity for scientific progress and political genius; the capacity for nihilism, exploitation, and terror. Because the author covers so much ground, from the discovery of radioactivity, through the development of the atomic bomb, he does not go into great depth on any one topic. Nonetheless, he paints vivid pictures of uranium's impact, including forced labor in Soviet mines and lucky prospectors who struck it rich in harsh environments, the spread of uranium smuggling, as well as an explanation of why it was absurd to claim that Saddam Hussein was attempting to purchase significant quantities of uranium from Niger. The only shortcoming is the author's omission of the issue of radioactive wastes generated by nuclear power. The author knows well what uranium looks like, why peril pulses in its every atom, and how scientists exploit its nuclear volatility. The drama is found in the weaponry uranium has spawned as demonstrated at Hiroshima and Nagasaki. In pursuit of this raw power, the U.S. let Navajos die extracting needed ore and let southwestern cities sicken beneath clouds from reckless testing. The Soviet Union sentenced tens of thousands to lethal gulag mines. Israel diverted ore through deception on the high seas. Pakistan stole European refining technology. Alive with devious personalities, the author's narrative ultimately exposes the frightening vulnerability of a world with too many sources of a dangerous substance and too little wisdom to control it

  17. Geochemical investigations by the U.S. Geological Survey on uranium mining, milling, and environmental restoration

    Science.gov (United States)

    Landa, Edward R.; Cravotta, Charles A.; Naftz, David L.; Verplanck, Philip L.; Nordstrom, D. Kirk; Zielinski, Robert A.

    2000-01-01

    Recent research by the U.S. Geological Survey has characterized contaminant sources and identified important geochemical processes that influence transport of radionuclides from uranium mining and milling wastes. 1) Selective extraction studies indicated that alkaline earth sulfates and hydrous ferric oxides are important hosts of 226Ra in uranium mill tailings. The action of sulfate-reducing and ironreducing bacteria on these phases was shown to enhance release of radium, and this adverse result may temper decisions to dispose of uranium mill tailings in anaerobic environments. 2) Field studies have shown that although surface-applied sewage sludge/wood chip amendments aid in revegetating pyritic spoil, the nitrogen in sludge leachate can enhance pyrite oxidation, acidification of groundwater, and the consequent mobilization of metals and radionuclides. 3) In a U.S. Environmental Protection Agencyfunded study, three permeable reactive barriers consisting of phosphate-rich material, zero-valent iron, or amorphous ferric oxyhydroxide have been installed at an abandoned uranium upgrader facility near Fry Canyon, UT. Preliminary results indicate that each of the permeable reactive barriers is removing the majority of the uranium from the groundwater. 4) Studies on the geochemistry of rare earth elements as analogues for actinides such as uranium and thorium in acid mine drainage environments indicate high mobility under acid-weathering conditions but measurable attenuation associated with iron and aluminum colloid formation. Mass balances from field and laboratory studies are being used to quantify the amount of attenuation. 5) A field study in Colorado demonstrated the use of 234U/238U isotopic ratio measurements to evaluate contamination of shallow groundwater with uranium mill effluent.

  18. SOLVENT EXTRACTION OF THORIUM VALUES FROM AQUEOUS SOLUTIONS

    Science.gov (United States)

    Warf, J.C.

    1959-04-21

    The separation of thorium values from rare earth metals contained ln aqueous solutions by means of extraction with a water immiscible alkyl phosphate diluted with a hydrocarbon such as hexane is described. While the extraction according to this invention may be carried out from any aqueous salt solution, it is preferred to use solutions containing free mineral acid. Hydrochloric acid and in particular nitric acid are sultable in a concentration ranging from 0.1 to 7 normal. The higher acid concentration results in higher extraction values.

  19. Gas-phase energetics of thorium fluorides and their ions.

    Science.gov (United States)

    Irikura, Karl K

    2013-02-14

    Gas-phase thermochemistry for neutral ThF(n) and cations ThF(n)(+) (n = 1-4) is obtained from large-basis CCSD(T) calculations, with a small-core pseudopotential on thorium. Electronic partition functions are computed with the help of relativistic MRCI calculations. Geometries, vibrational spectra, electronic fine structure, and ion appearance energies are tabulated. These results support the experimental results by Lau, Brittain, and Hildenbrand for the neutral species, except for ThF. The ion thermochemistry is presented here for the first time.

  20. Uranium hexafluoride handling. Proceedings

    Energy Technology Data Exchange (ETDEWEB)

    1991-12-31

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

  1. Mechanism of thorium biosorption by the cells of the soil fungal isolate Geotrichum sp. dwc-1

    Energy Technology Data Exchange (ETDEWEB)

    Ding, Congcong; Feng, Su [Sichuan Univ., Chengdu (China). Key Laboratory of Biological Resource and Ecological Environment; Li, Xiaolong [Sichuan Univ., Chengdu (China). Key Laboratory of Radiation Physics and Technology; and others

    2014-04-01

    In order to understand the impact of microorganisms on the fate of thorium in soils, we investigated the thorium biosorption behavior and the corresponding mechanisms by the cells of Geotrichum sp. dwc-1, one of the dominant species of fungal group isolated from 3.5 m depth soil layer in Southwest China. It was observed that fast thorium adsorption onto cells of G. sp. dwc-1 could take place, with a high distribution coefficient K{sub d} (0.93 mL/mg) obtained, when Geotrichum sp. dwc-1and thorium concentrations were 5 g/L and 10 mg/L, respectively. The thorium biosorption behavior was dependent on the pH value, and the lower pH could disrupt cell membrane of G. sp. dwc-1. At pH 1, thorium was accumulated in the cytoplasmic region of the cells. When pH was higher than 1, thorium was adsorbed on the cell surface of G. sp. dwc-1, like in periplasmic region or in the outer membrane. FTIR study combined with biosorption experiments further indicated that the thorium distribution and binding behavior on cell surface were associated with amino, hydroxyl groups and phosphate or sulphur functional groups, and might also be governed by electrostatic interaction. Moreover, PIXE and EPBS showed that ion-exchange mechanism contributed to the thorium biosorption process, in which the tetravalent thorium ions replaced smaller counter-ions (K{sup +}, Ca{sup 2+} and Fe{sup 3+}) occuring on the cell surface. (orig.)

  2. Gas Turbine Energy Conversion Systems for Nuclear Power Plants Applicable to LiFTR Liquid Fluoride Thorium Reactor Technology

    Science.gov (United States)

    Juhasz, Albert J.

    2014-01-01

    This panel plans to cover thermal energy and electric power production issues facing our nation and the world over the next decades, with relevant technologies ranging from near term to mid-and far term.Although the main focus will be on ground based plants to provide baseload electric power, energy conversion systems (ECS) for space are also included, with solar- or nuclear energy sources for output power levels ranging tens of Watts to kilo-Watts for unmanned spacecraft, and eventual mega-Watts for lunar outposts and planetary surface colonies. Implications of these technologies on future terrestrial energy systems, combined with advanced fracking, are touched upon.Thorium based reactors, and nuclear fusion along with suitable gas turbine energy conversion systems (ECS) will also be considered by the panelists. The characteristics of the above mentioned ECS will be described, both in terms of their overall energy utilization effectiveness and also with regard to climactic effects due to exhaust emissions.

  3. Uranium immobilization and nuclear waste

    Energy Technology Data Exchange (ETDEWEB)

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

    1982-02-01

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

  4. The Kintyre uranium project

    Energy Technology Data Exchange (ETDEWEB)

    Larson, B. [Canning Resources Pty. Ltd., Perth, WA (Australia)

    1997-12-31

    The Kintyre Uranium Project is being developed by Canning Resources Pty Ltd, a subsidiary of Rio Tinto (formerly CRA). The work on the project includes the planning and management of a number of background environmental studies. The company has also commissioned studies by external consultants into process technologies, mining strategies and techniques for extracting the uranium ore from the waste rock. In addition, Canning Resources has made a detailed assessment of the worldwide market potential for Australian uranium in the late 1990s and into the 21st century. The most significant factor affecting the future of this project is the current product price. This price is insufficient to justify the necessary investment to bring this project into production. 8 figs.

  5. Monitoring for thorium intakes by means of thoron (RN-220) in breath measurement; Inkorporationsueberwachung auf Thorium mittels RN-220-Exhalationsanalyse

    Energy Technology Data Exchange (ETDEWEB)

    Eisenmenger, A.; Riedel, W. [Freie Univ. Berlin (Germany). Universitaetsklinikum Benjamin Franklin; Brose, J.; Scheler, R. [Bundesamt fuer Strahlenschutz, Berlin (Germany)

    1998-12-31

    Thoron (Rn-220) in Breath Measurement is a sensitive method for routine monitoring of inhaled thorium intakes. Decay products of exhaled thoron (Po-216 and Pb-212), emanating from Thorium body burdens, are collected electrostatically and their progeny (esp. Po-212) are measured subsequently by alpha-spectrometry. The method has been optimized in respect to chamber volume, collection head geometry and position, supplied high voltage, breathing rate, humidity and counting time. Actually the method is capable to detect Th-228 in the lungs at a level as high as 3% of an Annual Limit on Intake, corresponding to 6 Bq of inhaled Th-228 (class W), as required by the German radiation protection monitoring guidelines. First measurements at occupationally exposed subjects in germany showed burdens up to 7,4 Bq Thorium in lungs derived from an exhalation rate of 3,7%. The amount of Th-232 results from the ratio of Th-228/Th-232 of the handeled material. Corresponding urine excretion analysis showed similar results. With in-vivo measurements no result above detection limit was found at all. (orig.) [Deutsch] Rn-220 Exhalationsmessungen sind eine sensible Methode zur Routineueberwachung von (inhalativen) Thoriuminkorporationen. Zerfallsprodukte des aus Thoriumkoerperdepots abgeatmeten Rn-220 (Po-216 und Pb-212) werden elektrostatisch gesammelt und deren Folgeprodukte dann alpha-spektrometrisch gemessen (spez. Po-212). Die Methode wurde in bezug auf das Sammelkammervolumen, die Sammelkopfgeometrie und -position, die angelegte Hochspannung, die Atemrate, die Atemfeuchtigkeit und die Messzeit optimiert. Derzeit ist es moeglich, mit dieser Methode 3% einer Jahresaktivitaetszufuhr ueber Inhalation in Bezug auf Th-228, entsprechend 6 Bq (Klasse W), nachzuweisen. Erste Messungen an beruflich Exponierten der Thorium-verarbeitenden Industrie in Deutschland zeigten Ergebnisse von bis 7,4 Bq Th-228 Lungendepots bei einer zugrunde gelegten Abatemrate von 3.7%. Der Th-232 Anteil ergibt sich

  6. PREPARATION OF URANIUM TRIOXIDE

    Science.gov (United States)

    Buckingham, J.S.

    1959-09-01

    The production of uranium trioxide from aqueous solutions of uranyl nitrate is discussed. The uranium trioxide is produced by adding sulfur or a sulfur-containing compound, such as thiourea, sulfamic acid, sulfuric acid, and ammonium sulfate, to the uranyl solution in an amount of about 0.5% by weight of the uranyl nitrate hexahydrate, evaporating the solution to dryness, and calcining the dry residue. The trioxide obtained by this method furnished a dioxide with a considerably higher reactivity with hydrogen fluoride than a trioxide prepared without the sulfur additive.

  7. 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.

  8. A Simplified Supercritical Fast Reactor with Thorium Fuel

    Directory of Open Access Journals (Sweden)

    Peng Zhang

    2014-01-01

    Full Text Available Super-Critical water-cooled Fast Reactor (SCFR is a feasible option for the Gen-IV SCWR designs, in which much less moderator and thus coolant are needed for transferring the fission heat from the core compared with the traditional LWRs. The fast spectrum of SCFR is useful for fuel breeding and thorium utilization, which is then beneficial for enhancing the sustainability of the nuclear fuel cycle. A SCFR core is constructed in this work, with the aim of simplifying the mechanical structure and keeping negative coolant void reactivity during the whole core life. A core burnup simulation scheme based on Monte Carlo lattice homogenization is adopted in this study, and the reactor physics analysis has been performed with DU-MOX and Th-MOX fuel. The main issues discussed include the fuel conversion ratio and the coolant void reactivity. The analysis shows that thorium-based fuel can provide inherent safety for SCFR without use of blanket, which is favorable for the mechanical design of SCFR.

  9. Nuclear feasibility study on thorium fueled PWR core

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Myung Hyun; Woo, Il Tak; Lim, Jae Yong; Ku, Bon Seung; Kim, Jong Chae; Lee, Sang Yun [Kyunghee University, Seoul (Korea)

    1999-04-01

    A computer code system, HELIOS and NESTLE or MASTER was established and checked for its reliability for the calculation of thorium fueled reactor. Previous results for the thorium fuel applications were evaluated including RTR reactor concept. Based on the detailed analysis on RTR, a new design concept was proposed. Characteristics of designed core should be checked for conversion ratio, nuclear design feasibility, proliferation resistance, fuel cycle economics, thermal-hydraulic safety, etc. Research was done only for the nuclear feasibility and high conversion in this 1st year. In order to seek for the design methodology, parametric studies were done for the following design parameters-fuel pin size, seed/blanket ratio, fuel material composition, and fissile enrichment. An optimization was done based on once-through fuel cycle with UO{sub 2} seed and (U, Th)O{sub 2} blanket. Economics, safety, non-proliferation, and waste transmutation will be checked in the future research works. (author). 19 refs., 39 figs., 39 tabs.

  10. Ten Top Tech Trends

    Science.gov (United States)

    McLester, Susan

    2008-01-01

    In this article, the author discusses the major technical issues, products, and practices of the day. The top ten tech trends are listed and discussed. These include: (1) data mining; (2) cyberbullying; (3) 21st century skills; (4) digital content; (5) learning at leisure; (6) personal responders; (7) mobile tools; (8) bandwidth; (9) open-source…

  11. Affordances: Ten Years On

    Science.gov (United States)

    Brown, Jill P.; Stillman, Gloria

    2014-01-01

    Ten years ago the construct, affordance, was rising in prominence in scholarly literature. A proliferation of different uses and meanings was evident. Beginning with its origin in the work of Gibson, we traced its development and use in various scholarly fields. This paper revisits our original question with respect to its utility in mathematics…

  12. Tens bij bevallingen

    NARCIS (Netherlands)

    Tuin-Nuis, F.D.F.

    2000-01-01

    TENS (Transcutane Electrische Neuro Stimulatie) is een pijnverlichtingsmethode die berust op de Gate Control Theory van Melzack en Wall. Door middel van electrische pulsen via de huid zou de geleiding van nociceptieve signalen (pijnprikkels) worden beïnvloed en zou het lichaam endorfinen aanmaken:

  13. Powers of ten

    CERN Multimedia

    Pyramid FILMS

    1977-01-01

    Powers of Ten is a 1977 short documentary film written and directed by Charles Eames and his wife, Ray. The film depicts the relative scale of the Universe in factors of ten (see also logarithmic scale and order of magnitude). The film begins with an aerial image of a man reclining on a blanket; the view is that of one meter across. The viewpoint, accompanied by expository voiceover, then slowly zooms out to a view ten meters across ( or 101 m in standard form), revealing that the man is picnicking in a park with a female companion. The zoom-out continues, to a view of 100 meters (102 m), then 1 kilometer (103 m), and so on, increasing the perspective—the picnic is revealed to be taking place near Soldier Field on Chicago's waterfront—and continuing to zoom out to a field of view of 1024 meters, or the size of the observable universe. The camera then zooms back in to the picnic, and then to views of negative powers of ten—10-1 m (10 centimeters), and so forth, until we are viewing a carbon nucl...

  14. URANIUM RECOVERY PROCESS

    Science.gov (United States)

    Hyman, H.H.; Dreher, J.L.

    1959-07-01

    The recovery of uranium from the acidic aqueous metal waste solutions resulting from the bismuth phosphate carrier precipitation of plutonium from solutions of neutron irradiated uranium is described. The waste solutions consist of phosphoric acid, sulfuric acid, and uranium as a uranyl salt, together with salts of the fission products normally associated with neutron irradiated uranium. Generally, the process of the invention involves the partial neutralization of the waste solution with sodium hydroxide, followed by conversion of the solution to a pH 11 by mixing therewith sufficient sodium carbonate. The resultant carbonate-complexed waste is contacted with a titanated silica gel and the adsorbent separated from the aqueous medium. The aqueous solution is then mixed with sufficient acetic acid to bring the pH of the aqueous medium to between 4 and 5, whereby sodium uranyl acetate is precipitated. The precipitate is dissolved in nitric acid and the resulting solution preferably provided with salting out agents. Uranyl nitrate is recovered from the solution by extraction with an ether such as diethyl ether.

  15. URANIUM SOLVENT EXTRACTION PROCESS

    Science.gov (United States)

    Harrington, C.D.

    1959-09-01

    A method is given for extracting uranium values from ores of high phosphate content consisting of dissolving them in aqueous nitric acid, adjusting the concentration of the aqueous solution to about 2 M with respect to nitric acid, and then contacting it with diethyl ether which has previously been made 1 M with respect to nitric acid.

  16. Uranium from seawater

    Energy Technology Data Exchange (ETDEWEB)

    Gregg, D.; Folkendt, M.

    1982-09-21

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

  17. Uranium hydrogeochemical and stream sediment reconnaissance of the Arminto NTMS quadrangle, Wyoming, including concentrations of forty-three additional elements

    Energy Technology Data Exchange (ETDEWEB)

    Morgan, T.L.

    1979-11-01

    During the summers of 1976 and 1977, 570 water and 1249 sediment samples were collected from 1517 locations within the 18,000-km/sup 2/ area of the Arminto NTMS quadrangle of central Wyoming. Water samples were collected from wells, springs, streams, and artifical ponds; sediment samples were collected from wet and dry streams, springs, and wet and dry ponds. All water samples were analyzed for 13 elements, including uranium, and each sediment sample was analyzed for 43 elements, including uranium and thorium. Uranium concentrations in water samples range from below the detection limit to 84.60 parts per billion (ppb) with a mean of 4.32 ppb. All water sample types except pond water samples were considered as a single population in interpreting the data. Pond water samples were excluded due to possible concentration of uranium by evaporation. Most of the water samples containing greater than 20 ppb uranium grouped into six clusters that indicate possible areas of interest for further investigation. One cluster is associated with the Pumpkin Buttes District, and two others are near the Kaycee and Mayoworth areas of uranium mineralization. The largest cluster is located on the west side of the Powder River Basin. One cluster is located in the central Big Horn Basin and another is in the Wind River Basin; both are in areas underlain by favorable host units. Uranium concentrations in sediment samples range from 0.08 parts per million (ppm) to 115.50 ppm with a mean of 3.50 ppm. Two clusters of sediment samples over 7 ppm were delineated. The first, containing the two highest-concentration samples, corresponds with the Copper Mountain District. Many of the high uranium concentrations in samples in this cluster may be due to contamination from mining or prospecting activity upstream from the sample sites. The second cluster encompasses a wide area in the Wind River Basin along the southern boundary of the quadrangle.

  18. Ten Utah Painters

    OpenAIRE

    Whitlock, Andrew

    1984-01-01

    Today the art world is rich and diverse with regional as well as national art centers. As in the past, art is alive and well in Utah. The show Ten Utah Painters invites us to see and experiece what some of Utah's best contemporary artists are doing. Their paintings invite us to look and to enjoy but also to learn and open up our visual senses to a broader vista.

  19. Uranium in soils integrated demonstration site characterization at Fernald, Ohio. Report of uranium concentrations in soil determined by in situ LA-ICP-AES

    Energy Technology Data Exchange (ETDEWEB)

    Baldwin, D.; Zamzow, D.; Bajic, S.J. [and others

    1993-02-02

    Laser ablation-inductively coupled plasma-atomic emission spectrometry was used for in situ determination of uranium and thorium concentrations in soil at 80 sampling sites in the Sewage Treatment Plant area. This work was performed by the Environmental Technology Development Program of the Ames Laboratory using a completely self-contained mobile laboratory. This laboratory, the mobile demonstration laboratory for environmental screening technologies and the robotic sampling accessory, were designed and constructed by the Ames Laboratory during FY 1992. The instrumentation is capable of analyzing each sample for twenty operator-defined elements simultaneously. Using the MDLEST/RSA, the uranium concentrations in the soil at the 80 sampling sites were found to range from <20 parts-per-million (ppM)(<13.5 pCi/g) to 303 ppM (205 pCi/g). The 95% confidence interval for these field determined values range from 80 to 110 ppM. Bore hole samples from two sites were analyzed. No measurable uranium concentration was detected below the one foot depth. Seven samples taken from sites within an area currently under remediation were analyzed and found to contain uranium concentrations ranging from 101 ppM (68.3 pCi/g) to 788 ppM (532 pCi/g). Soil samples were taken from twelve of the 80 sampling sites in the field, using conventional sampling techniques. These samples were prepared by microwave digestion, using the wet chemistry capability in the MDLEST, and field analyzed using solution nebulization ICP-AES. The laboratory procedure followed for microwave digestion required the samples to be diluted by a factor of 100. This dilution resulted in uranium intensities too low to be accurately quantitated in the field. Optimization of the instrumentation and sample preparation will make this field capability useful in determining near real-time the soil matrix, and enable the performance of this quality assurance process in the field with greater sensitivity and accuracy.

  20. Diffusion in thorium carbide: A first-principles study

    Energy Technology Data Exchange (ETDEWEB)

    Pérez Daroca, D., E-mail: pdaroca@tandar.cnea.gov.ar [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica, Av. General Paz 1499, 1650, San Martín, Buenos Aires (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas, 1025, Buenos Aires (Argentina); Llois, A.M. [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica, Av. General Paz 1499, 1650, San Martín, Buenos Aires (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas, 1025, Buenos Aires (Argentina); Mosca, H.O. [Gerencia de Investigación y Aplicaciones, Comisión Nacional de Energía Atómica, Av. General Paz 1499, 1650, San Martín, Buenos Aires (Argentina); Instituto de Tecnología Jorge A. Sabato, UNSAM–CNEA, Av. General Paz 1499, 1650, San Martín, Buenos Aires (Argentina)

    2015-12-15

    The prediction of the behavior of Th compounds under irradiation is an important issue for the upcoming Generation-IV nuclear reactors. The study of self-diffusion and hetero-diffusion is a central key to fulfill this goal. As a first approach, we obtained, by means of first-principles methods, migration and activation energies of Th and C atoms self-diffusion and diffusion of He atoms in ThC. We also calculate diffusion coefficients as a function of temperature. - Highlights: • Diffusion in thorium carbide by means of first-principles calculations is studied. • The most favorable migration event is a C atom moving through a C-vacancy aided path. • Calculated C atoms diffusion coefficients agree very well with the experimental data. • For He, the energetically most favorable migration path is through Th-vacancies.

  1. Burnup calculations using serpent code in accelerator driven thorium reactors

    Energy Technology Data Exchange (ETDEWEB)

    Korkmaz, M.E.; Agar, O. [Karamanoglu Mehmetbey Univ., Karaman (Turkey). Physics Dept.; Yigit, M. [Aksaray Univ. (Turkey). Physics Dept.

    2013-07-15

    In this study, burnup calculations have been performed for a sodium cooled Accelerator Driven Thorium Reactor (ADTR) using the Serpent 1.1.16 Monte Carlo code. The ADTR has been designed for burning minor actinides, mixed {sup 232}Th and mixed {sup 233}U fuels. A solid Pb-Bi spallation target in the center of the core is used and sodium as coolant. The system is designed for a heating power of 2 000 MW and for an operation time of 600 days. For burnup calculations the Advanced Matrix Exponential Method CRAM (Chebyshev Rational Approximation Method) and different nuclear data libraries (ENDF7, JEF2.2, JEFF3.1.1) were used. The effective multiplication factor change from 0.93 to 0.97 for different nuclear data libraries during the reactor operation period. (orig.)

  2. DE-NE0000735 - FINAL REPORT ON THORIUM FUEL CYCLE NEUP PROJECT

    Energy Technology Data Exchange (ETDEWEB)

    Krahn, Steven [Vanderbilt Univ., Nashville, TN (United States); Ault, Timothy [Vanderbilt Univ., Nashville, TN (United States); Worrall, Andrew [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2017-09-30

    The report is broken into six chapters, including this executive summary chapter. Following an introduction, this report discusses each of the project’s three major components (Fuel Cycle Data Package (FCDP) Development, Thorium Fuel Cycle Literature Analysis and Database Development, and the Thorium Fuel Cycle Technical Track and Proceedings). A final chapter is devoted to summarization. Various outcomes, publications, etc. originating from this project can be found in the Appendices at the end of the document.

  3. The Growth of Monoraphidium sp. and Scenedesmus sp. Cells in the Presence of Thorium

    Directory of Open Access Journals (Sweden)

    Juliana Cristina de Queiroz

    2012-01-01

    Full Text Available Toxicity of thorium by Monoraphidium sp. and Scenedesmus sp. was studied. Microalgal cultures were inoculated in ASM-1 medium in presence and absence of thorium. Its effect was monitored by direct counting on Fuchs-Rosenthal chamber and with software. The toxicity of thorium over the species was observed for concentrations over 50.0 mg/L. After 30 days, Monoraphidium cells decreased their concentration from 4.23×106 to 4.27×105 and 8.57×105 cells/mL, in the presence of 50.0 and 100.0 mg/L of thorium, respectively. Scenedesmus sp. cells were more resistant to thorium: for an initial cell concentration of 7.65×104 cells/mL it was observed a change to 5.25×105 and 5.12×105 cells/mL, in the presence of thorium at 50.0 and 100.0 mg/L, respectively. This is an indication that low concentrations of the radionuclide favored the growth, and that Scenedesmus cells are more resistant to thorium than Monoraphidium cells. The software used for comparison with direct count method proved to be useful for the improvement of accuracy of the results obtained, a decrease in the uncertainty and allowed recording of the data. The presence of thorium suggests that low concentrations have a positive effect on the growth, due to the presence of the nitrate, indicating its potential for ecotoxicological studies.

  4. The Growth of Monoraphidium sp. and Scenedesmus sp. Cells in the Presence of Thorium

    Science.gov (United States)

    de Queiroz, Juliana Cristina; Ferreira, Ana Cristina de Melo; da Costa, Antonio Carlos Augusto

    2012-01-01

    Toxicity of thorium by Monoraphidium sp. and Scenedesmus sp. was studied. Microalgal cultures were inoculated in ASM-1 medium in presence and absence of thorium. Its effect was monitored by direct counting on Fuchs-Rosenthal chamber and with software. The toxicity of thorium over the species was observed for concentrations over 50.0 mg/L. After 30 days, Monoraphidium cells decreased their concentration from 4.23 × 106 to 4.27 × 105 and 8.57 × 105 cells/mL, in the presence of 50.0 and 100.0 mg/L of thorium, respectively. Scenedesmus sp. cells were more resistant to thorium: for an initial cell concentration of 7.65 × 104 cells/mL it was observed a change to 5.25 × 105 and 5.12 × 105 cells/mL, in the presence of thorium at 50.0 and 100.0 mg/L, respectively. This is an indication that low concentrations of the radionuclide favored the growth, and that Scenedesmus cells are more resistant to thorium than Monoraphidium cells. The software used for comparison with direct count method proved to be useful for the improvement of accuracy of the results obtained, a decrease in the uncertainty and allowed recording of the data. The presence of thorium suggests that low concentrations have a positive effect on the growth, due to the presence of the nitrate, indicating its potential for ecotoxicological studies. PMID:22649297

  5. New Twists and Turns for Actinide Chemistry: Organometallic Infinite Coordination Polymers of Thorium Diazide.

    Science.gov (United States)

    Monreal, Marisa J; Seaman, Lani A; Goff, George S; Michalczyk, Ryszard; Morris, David E; Scott, Brian L; Kiplinger, Jaqueline L

    2016-03-07

    Two organometallic 1D infinite coordination polymers and two organometallic monometallic complexes of thorium diazide have been synthesized and characterized. Steric control of these self-assembled arrays, which are dense in thorium and nitrogen, has also been demonstrated: infinite chains can be circumvented by using steric bulk either at the metallocene or with a donor ligand in the wedge. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. New twists and turns for actinide chemistry: organometallic infinite coordination polymers of thorium diazide

    Energy Technology Data Exchange (ETDEWEB)

    Monreal, Marisa J.; Seaman, Lani A.; Goff, George S.; Michalczyk, Ryszard; Morris, David E.; Scott, Brian L.; Kiplinger, Jaqueline L. [Los Alamos National Laboratory, Los Alamos, NM (United States)

    2016-03-07

    Two organometallic 1D infinite coordination polymers and two organometallic monometallic complexes of thorium diazide have been synthesized and characterized. Steric control of these self-assembled arrays, which are dense in thorium and nitrogen, has also been demonstrated: infinite chains can be circumvented by using steric bulk either at the metallocene or with a donor ligand in the wedge. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  7. Uranium Mines and Mills Location Database

    Science.gov (United States)

    The Uranium Mines and Mills location database identifies and shows the location of active and inactive uranium mines and mills, as well as mines which principally produced other minerals, but were known to have uranium in the ore.

  8. Radiochemistry of uranium

    Energy Technology Data Exchange (ETDEWEB)

    Gindler, J.E.

    1962-03-01

    This volume which deals with the radiochemistry of uranium is one of a series of monographs on radiochemistry of the elements. There is included a review of the nuclear and chemical features of particular interest to the radiochemist, a discussion of problems of dissolution of a sample and counting technique, and finally, a collection of radiochemical procedures for the element as found in the literature.

  9. Raw material uranium; Rohstoff Uran

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2017-03-15

    Uranium is an important raw material in human life. Mostly using nuclear fission uranium is used in nuclear medicine, industry and research. The most important application is the generation of electricity in nuclear power plants. Due to the global availability the worldwide uranium supply is guaranties for a long time. The contribution covers the issues medicine, neutron research, energy generation, occurrence, mining, processing, recycling and disposal.

  10. Biological pathways of exposure and ecotoxicity values for uranium and associated radionuclides: Chapter D in Hydrological, geological, and biological site characterization of breccia pipe uranium deposits in Northern Arizona

    Science.gov (United States)

    Hinck, Jo E.; Linder, Greg L.; Finger, Susan E.; Little, Edward E.; Tillitt, Donald E.; Kuhne, Wendy

    2010-01-01

    This chapter compiles available chemical and radiation toxicity information for plants and animals from the scientific literature on naturally occurring uranium and associated radionuclides. Specifically, chemical and radiation hazards associated with radionuclides in the uranium decay series including uranium, thallium, thorium, bismuth, radium, radon, protactinium, polonium, actinium, and francium were the focus of the literature compilation. In addition, exposure pathways and a food web specific to the segregation areas were developed. Major biological exposure pathways considered were ingestion, inhalation, absorption, and bioaccumulation, and biota categories included microbes, invertebrates, plants, fishes, amphibians, reptiles, birds, and mammals. These data were developed for incorporation into a risk assessment to be conducted as part of an environmental impact statement for the Bureau of Land Management, which would identify representative plants and animals and their relative sensitivities to exposure of uranium and associated radionuclides. This chapter provides pertinent information to aid in the development of such an ecological risk assessment but does not estimate or derive guidance thresholds for radionuclides associated with uranium. Previous studies have not attempted to quantify the risks to biota caused directly by the chemical or radiation releases at uranium mining sites, although some information is available for uranium mill tailings and uranium mine closure activities. Research into the biological impacts of uranium exposure is strongly biased towards human health and exposure related to enriched or depleted uranium associated with the nuclear energy industry rather than naturally occurring uranium associated with uranium mining. Nevertheless, studies have reported that uranium and other radionuclides can affect the survival, growth, and reproduction of plants and animals. Exposure to chemical and radiation hazards is influenced by a

  11. Uranium Carbide Powder Ignition Studies

    Energy Technology Data Exchange (ETDEWEB)

    Berthinier, C.; Coullomb, S.; Rado, C.; Le Guyadec, F. [CEA, DEN, DTEC, SDTC, LEME, F-30207 Bagnols-sur-Ceze (France); Chatillon, C.; Blanquet, E.; Boichot, R. [SIMAP, Sciences et Ingenierie des Materiaux et Procedes, INPG-CNRS-UJF ENSEEG, BP 75, 38402 St Martin-d' Heres (France)

    2009-06-15

    Mixed (U, Pu) carbide, constituted by means of 80% of uranium monocarbide (UC), is considered as a possible fuel material for future gas fast reactors or sodium fast reactor. However, UC undergoes a strong exothermic reaction with air and fine powders of UC are pyrophoric. Thus, it is necessary to understand this high reactivity in order to determine safe handling conditions for the production and reprocessing of carbide fuels. UC powder was obtained by arc melting and milling. The reactivity of uranium carbide was studied in oxidizing atmosphere and different experimental devices were used to determine ignition temperatures. The phases formed at the various observed stages of the oxidation process were determined by post-mortem X ray diffraction analysis. Studies were first performed using small quantities of UC powder (around 50 mg) in Differential Thermal Analysis / Thermogravimetric Analysis (DTA/TGA) and Differential Scanning Calorimetry (DSC). Experiments were realized using different parameters, such as heating rate and gas flow rate and composition, to determine their influence on pyro-phoricity. Results obtained with small quantities (tens of milligrams) revealed that UC powder is highly reactive in air in the range 200- 250 deg. C. Studies were also performed in the 'Pyro' test facility multi-function furnace allowing CCD camera recording, during heating and ignition, through view-ports. Lower ignition temperatures, around 100 deg. C, were obtained using around 1 g UC powder samples. Results are discussed and analysed with theory of burning curve ignition and numerical simulations. Simulations aim to understand the influence of the different parameters on pyro-phoricity. Small scale simulations (on a spherical grain) confirm the influence of UC grains size, heat rate and gas composition on powder ignition temperature with small quantities. The issue is now to understand the influence of grain pile form factor and volume on the pyro-phoricity of

  12. Safety evaluation for packaging (onsite) depleted uranium waste boxes

    Energy Technology Data Exchange (ETDEWEB)

    McCormick, W.A.

    1997-08-27

    This safety evaluation for packaging (SEP) allows the one-time shipment of ten metal boxes and one wooden box containing depleted uranium material from the Fast Flux Test Facility to the burial grounds in the 200 West Area for disposal. This SEP provides the analyses and operational controls necessary to demonstrate that the shipment will be safe for the onsite worker and the public.

  13. Uranium prospecting; La prospection de l'uranium

    Energy Technology Data Exchange (ETDEWEB)

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

    1955-07-01

    This report is an instruction book for uranium prospecting. It appeals to private prospecting. As prospecting is now a scientific and technical research, it cannot be done without preliminary studies. First of all, general prospecting methods are given with a recall of fundamental geologic data and some general principles which are common with all type of prospecting. The peculiarities of uranium prospecting are also presented and in particular the radioactivity property of uranium as well as the special aspect of uranium ores and the aspect of neighbouring ores. In a third part, a description of the different uranium ores is given and separated in two different categories: primary and secondary ores, according to the place of transformation, deep or near the crust surface respectively. In the first category, the primary ores include pitchblende, thorianite and rare uranium oxides as euxenite and fergusonite for example. In the second category, the secondary ores contain autunite and chalcolite for example. An exhaustive presentation of the geiger-Mueller counter is given with the presentation of its different components, its functioning and utilization and its maintenance. The radioactivity interpretation method is showed as well as the elaboration of a topographic map of the measured radioactivity. A brief presentation of other detection methods than geiger-Mueller counters is given: the measurement of fluorescence and a chemical test using the fluorescence properties of uranium salts. Finally, the main characteristics of uranium deposits are discussed. (M.P.)

  14. FLAME DENITRATION AND REDUCTION OF URANIUM NITRATE TO URANIUM DIOXIDE

    Science.gov (United States)

    Hedley, W.H.; Roehrs, R.J.; Henderson, C.M.

    1962-06-26

    A process is given for converting uranyl nitrate solution to uranium dioxide. The process comprises spraying fine droplets of aqueous uranyl nitrate solution into a hightemperature hydrocarbon flame, said flame being deficient in oxygen approximately 30%, retaining the feed in the flame for a sufficient length of time to reduce the nitrate to the dioxide, and recovering uranium dioxide. (AEC)

  15. Preliminary study of a radiological survey in an abandoned uranium mining area in Madagascar

    Science.gov (United States)

    N, Rabesiranana; M, Rasolonirina; F, Solonjara A.; Andriambololona., Raoelina; L, Mabit

    2010-05-01

    The region of Vinaninkarena located in central Madagascar (47°02'40"E, 19°57'17"S), is known to be a high natural radioactive area. Uranium ore was extracted in this region during the 1950s and the early 1960s. In the mid-1960s, mining activities were stopped and the site abandoned. In the meantime, the region, which used to be without any inhabitants, has recently been occupied by new settlers with presumed increase in exposure of the local population to natural ionizing radiation. In order to assess radiological risk, a survey to assess the soil natural radioactivity background was conducted during the year 2004. This study was implemented in the frame of the FADES Project SP99v1b_21 entitled: Assessment of the environmental pollution by multidisciplinary approach, and the International Atomic Energy Agency Technical Cooperation Project MAG 7002 entitled: Effects of air and water pollution on human health. Global Positioning System (GPS) was used to determine the geographical coordinates of the top soil samples (0-15cm) collected. The sampling was performed using a multi integrated scale approach to estimate the spatial variability of the parameters under investigation (U, Th and K) using geo-statistical approach. A total of 205 soil samples was collected in the study site (16 km2). After humidity correction, the samples were sealed in 100 cm3 cylindrical air-tight plastic containers and stored for more than 6 months to reach a secular equilibrium between parents and short-lived progeny (226Ra and progeny, 238U and 234Th). Measurements were performed using a high-resolution HPGe Gamma-detector with a 30% relative efficiency and an energy resolution of 1.8 keV at 1332.5 keV, allowing the determination of the uranium and thorium series and 40K. In case of secular equilibrium, a non-gamma-emitting radionuclide activity was deduced from its gamma emitting progeny. This was the case for 238U (from 234Th), 226Ra (from 214Pb and 214Bi) and 232Th (from 228Ac, 212Pb or

  16. Uranium in soils and water; Uran in Boden und Wasser

    Energy Technology Data Exchange (ETDEWEB)

    Dienemann, Claudia; Utermann, Jens

    2012-07-15

    The report of the Umweltbundesamt (Federal Environmental Agency) on uranium in soils and water covers the following chapters: (1) Introduction. (2) Deposits and properties: Use of uranium; toxic effects on human beings, uranium in ground water and drinking water, uranium in surface waters, uranium in soils, uranium in the air. (3) Legal regulations. (4) Uranium deposits, uranium mining, polluted area recultivation. (5) Diffuse uranium entry in soils and water: uranium insertion due to fertilizers, uranium insertion due to atmospheric precipitation, uranium insertion from the air. (6) Diffuse uranium release from soils and transfer in to the food chain. (7) Conclusions and recommendations.

  17. Aluminosilicate Precipitation Impact on Uranium

    Energy Technology Data Exchange (ETDEWEB)

    WILMARTH, WILLIAM

    2006-03-10

    Experiments have been conducted to examine the fate of uranium during the formation of sodium aluminosilicate (NAS) when wastes containing high aluminate concentrations are mixed with wastes of high silicate concentration. Testing was conducted at varying degrees of uranium saturation. Testing examined typical tank conditions, e.g., stagnant, slightly elevated temperature (50 C). The results showed that under sub-saturated conditions uranium is not removed from solution to any large extent in both simulant testing and actual tank waste testing. This aspect was not thoroughly understood prior to this work and was necessary to avoid criticality issues when actual tank wastes were aggregated. There are data supporting a small removal due to sorption of uranium on sites in the NAS. Above the solubility limit the data are clear that a reduction in uranium concentration occurs concomitant with the formation of aluminosilicate. This uranium precipitation is fairly rapid and ceases when uranium reaches its solubility limit. At the solubility limit, it appears that uranium is not affected, but further testing might be warranted.

  18. SOLVENT EXTRACTION OF URANIUM VALUES

    Science.gov (United States)

    Feder, H.M.; Ader, M.; Ross, L.E.

    1959-02-01

    A process is presented for extracting uranium salt from aqueous acidic solutions by organic solvent extraction. It consists in contacting the uranium bearing solution with a water immiscible dialkylacetamide having at least 8 carbon atoms in the molecule. Mentioned as a preferred extractant is dibutylacetamide. The organic solvent is usually used with a diluent such as kerosene or CCl/sub 4/.

  19. High priority nuclear data request list. The data for long-lived fission products, minor actinides and the thorium cycle

    Energy Technology Data Exchange (ETDEWEB)

    Rowlands, J. [Organisation for Economic Co-Operation and Development, Nuclear Energy Agency, 75 - Paris (France)

    2002-07-01

    This workshop is organised by the Research Group GEDEON together with CERN, OECD-NEA and the CFDN (French Committee for Nuclear Data). It is the continuation of the one at CERN on September 21 and 22, 1998, jointly organised with EC, GEDEON and OCDE-NEA. This last one is centred on the CERN proposal of a facility for neutron production up to 250 MeV, devoted to neutron data measurements. The first aim of the Paris workshop is to identify the present status of specific nuclear data relevant to innovative options (accelerator driven system - ADS and thorium) in the nuclear fuel cycle, beyond what has been gathered for standard reactors (PWR, FBR) and for the associated fuel cycles based on uranium and plutonium. The following topics were presented and discussed: 1. extension of present evaluated nuclear data files beyond 20 MeV needed to correctly describe the high energy part (up to approximately 200 MeV) of the spallation process used to generate the external neutrons needed for the sub-critical assemblies; 2. differential and integral cross section data in relation with the use of a thorium based; 3. the same for minor actinides and some long-lived fission residues likely to be destroyed in reactors; 4. the same for new type of materials such as lead or lead-bismuth, to be used as spallation target or as cooling, in relation with corrosion and irradiation effects. Beyond these specific issues, ADS will also take advantage of better known nuclear data coming from the existing reactors in operation. Very recent results related to spallation target physics such as neutron and residues production from heavy targets were also presented at this workshop. One very important aim of this workshop is also to bring physicists from different origin, especially from CERN, to cooperate in a program on nuclear data in relation with innovative options. This document brings together two articles entitled ''high priority nuclear data request list. The data for long lived

  20. The ten thousand Kims

    Science.gov (United States)

    Baek, Seung Ki; Minnhagen, Petter; Kim, Beom Jun

    2011-07-01

    In Korean culture, the names of family members are recorded in special family books. This makes it possible to follow the distribution of Korean family names far back in history. It is shown here that these name distributions are well described by a simple null model, the random group formation (RGF) model. This model makes it possible to predict how the name distributions change and these predictions are shown to be borne out. In particular, the RGF model predicts that for married women entering a collection of family books in a certain year, the occurrence of the most common family name 'Kim' should be directly proportional to the total number of married women with the same proportionality constant for all the years. This prediction is also borne out to a high degree. We speculate that it reflects some inherent social stability in the Korean culture. In addition, we obtain an estimate of the total population of the Korean culture down to the year 500 AD, based on the RGF model, and find about ten thousand Kims.

  1. Radionuclides in waters and soil near the Lagoa Real uranium mine

    Energy Technology Data Exchange (ETDEWEB)

    Souza, Susana Oliveira de; Freire, Fabinara Dantas, E-mail: sosouza@ufs.br [Universidade Federal de Sergipe (UFS), Sao Cristovao, SE (Brazil). Departamento de Fisica; Kozlowska, Beata; Walencik-Lata, Agata, E-mail: beata.kozlowska@us.edu.pl [University of Silesia, Institute of Physics, Katowice (Poland); Dias, Dario M., E-mail: engenheirodario@gmail.com [Secretaria Municipal de Meio Ambiente e Turismo, Andarai, BA (Brazil); Veiga, Artur Jose Pires, E-mail: tk1@ibest.com [Universidade Estadual do Sudoeste da Bahia (UESB), Itapetinga, BA (Brazil). Departamento de Ciencias Exatas e Tecnologicas

    2015-07-01

    Uranium mining generates fuel for the nuclear power plants and it is the main source of income for the region of Caetite-BA. However, Non-Governmental Organizations claim that mining pollutes the environment and jeopardizes human health and safety. Besides uranium, the ground contains significant concentrations of thorium and of all radionuclides of its family, such as radium isotopes. In this framework, we carried out an independent study analyzing the concentration of the radionuclides activities {sup 226,} {sup 228}Ra and {sup 234,238}U in water samples and radionuclides {sup 226}Ra, {sup 232}Th and {sup 40}K in soil samples using different techniques of nuclear spectrometry. The selection criteria for the collection points were their proximity to the uranium processing plant and to affluent rivers. The soil samples presented very low concentration of activity for radionuclides investigated, compared to the limits established of the exclusion, exemption and impartiality for radiation protection requirement given by the Regulator Position established by CNEN. The amount of radioisotopes appears consistent with a natural origin, thus it is not possible to state that the mining process in Caetite increases pollution or radiation exposure in a significant way. (author)

  2. TRISO Fuel Performance: Modeling, Integration into Mainstream Design Studies, and Application to a Thorium-fueled Fusion-Fission Hybrid Blanket

    Energy Technology Data Exchange (ETDEWEB)

    Powers, Jeffrey James [Univ. of California, Berkeley, CA (United States)

    2011-11-30

    This study focused on creating a new tristructural isotropic (TRISO) coated particle fuel performance model and demonstrating the integration of this model into an existing system of neutronics and heat transfer codes, creating a user-friendly option for including fuel performance analysis within system design optimization and system-level trade-off studies. The end product enables both a deeper understanding and better overall system performance of nuclear energy systems limited or greatly impacted by TRISO fuel performance. A thorium-fueled hybrid fusion-fission Laser Inertial Fusion Energy (LIFE) blanket design was used for illustrating the application of this new capability and demonstrated both the importance of integrating fuel performance calculations into mainstream design studies and the impact that this new integrated analysis had on system-level design decisions. A new TRISO fuel performance model named TRIUNE was developed and verified and validated during this work with a novel methodology established for simulating the actual lifetime of a TRISO particle during repeated passes through a pebble bed. In addition, integrated self-consistent calculations were performed for neutronics depletion analysis, heat transfer calculations, and then fuel performance modeling for a full parametric study that encompassed over 80 different design options that went through all three phases of analysis. Lastly, side studies were performed that included a comparison of thorium and depleted uranium (DU) LIFE blankets as well as some uncertainty quantification work to help guide future experimental work by assessing what material properties in TRISO fuel performance modeling are most in need of improvement. A recommended thorium-fueled hybrid LIFE engine design was identified with an initial fuel load of 20MT of thorium, 15% TRISO packing within the graphite fuel pebbles, and a 20cm neutron multiplier layer with beryllium pebbles in flibe molten salt coolant. It operated

  3. Preserving Ultra-Pure Uranium-233

    Energy Technology Data Exchange (ETDEWEB)

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

    2011-10-01

    Uranium-233 ({sup 233}U) is a synthetic isotope of uranium formed under reactor conditions during neutron capture by natural thorium ({sup 232}Th). At high purities, this synthetic isotope serves as a crucial reference material for accurately quantifying and characterizing uranium-bearing materials assays and isotopic distributions for domestic and international nuclear safeguards. Separated, high purity {sup 233}U is stored in vaults at Oak Ridge National Laboratory (ORNL). These materials represent a broad spectrum of {sup 233}U from the standpoint of isotopic purity - the purest being crucial for precise analyses in safeguarding uranium. All {sup 233}U at ORNL is currently scheduled to be disposed of by down-blending with depleted uranium beginning in 2015. This will reduce safety concerns and security costs associated with storage. Down-blending this material will permanently destroy its potential value as a certified reference material for use in uranium analyses. Furthermore, no credible options exist for replacing {sup 233}U due to the lack of operating production capability and the high cost of restarting currently shut down capabilities. A study was commissioned to determine the need for preserving high-purity {sup 233}U. This study looked at the current supply and the historical and continuing domestic need for this crucial isotope. It examined the gap in supplies and uses to meet domestic needs and extrapolated them in the context of international safeguards and security activities - superimposed on the recognition that existing supplies are being depleted while candidate replacement material is being prepared for disposal. This study found that the total worldwide need by this projection is at least 850 g of certified {sup 233}U reference material over the next 50 years. This amount also includes a strategic reserve. To meet this need, 18 individual items totaling 959 g of {sup 233}U were identified as candidates for establishing a lasting supply of

  4. The Liquid Fluoride Thorium Reactor: Energy Cheaper Than Coal

    Science.gov (United States)

    Stone, Cavan

    2011-11-01

    This century, we face significant environmental challenges. Our demand for limited natural resources is rapidly increasing and much of humanity is concerned about the consequences. Our unsustainably growing population drives these challenges, and humanely stabilizing it would alleviate these pressures. Demographic data clearly shows that prosperity stabilizes population and it also shows that prosperity critically requires energy. In spite of the pressing and demonstrable nature of these challenges however, politically there is no international consensus on global energy policy. Developing nations simply will not accept a policy that will hamper their economic growth. Yet, we do have a solution to these challenges, an idea conceived and experimentally tested by Alvin Weinberg at Oak Ridge National Laboratory, the Liquid Fluoride Thorium Reactor. Presently, various laboratories and start-up companies, including the Chinese Academy of Sciences have begun efforts to commercialize the technology. By delivering the promise of inexpensive energy it will be in the economic interest of the developing nations to use this carbon-free energy source. By delivering superior performance on longstanding public concerns about nuclear energy, it will be technologically and politically feasible for developing nations to stabilize their population with the bounty of energy cheaper than coal.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1947-03-10

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

  6. PREPARATION OF URANIUM-ALUMINUM ALLOYS

    Science.gov (United States)

    Moore, R.H.

    1962-09-01

    A process is given for preparing uranium--aluminum alloys from a solution of uranium halide in an about equimolar molten alkali metal halide-- aluminum halide mixture and excess aluminum. The uranium halide is reduced and the uranium is alloyed with the excess aluminum. The alloy and salt are separated from each other. (AEC)

  7. Natural radionuclides in effluents release by a deactivated uranium mine

    Energy Technology Data Exchange (ETDEWEB)

    Pereira, Wagner S.; Kelecom, Alphonse; Silva, Ademir X.; Lopes, José M.; Pinto, Carlos E.C.; Py Júnior, Delcy A.; Antunes, Marcos M., E-mail: pereiraws@gmail.com, E-mail: caerjbr@gmail.com, E-mail: wspereira@inb.gov.br, E-mail: delcy@inb.gov.br, E-mail: Antunes@inb.gov.br, E-mail: lararapls@hotmail.com, E-mail: Ademir@nuclear.ufrj.br, E-mail: marqueslopes@yahoo.com.br [Universidade Veiga de Almeida (UVA), Rio de Janeiro, RJ (Brazil); Indústrias Nucleares do Brasil (COMAP.N/FCN/INB), Resende RJ (Brazil). Fábrica de Combustível Nuclear. Coordenação de Meio Ambiente e Proteção Radiológica Ambiental; Universidade Federal Fluminense (LARARA-PLS/UFF), Niterói, RJ (Brazil). Laboratório de Radiobiologia e Radiometria; Coordenacao de Pos-Graduacao e Pesquisa de Engenharia (COPPE/UFRJ), Rio de Janeiro, RJ (Brazil). Programa de Engenharia Nuclear

    2017-07-01

    The Ore Treatment Unit (OTU) is a mine and deactivated uranium plant in the city of Caldas, Minas Gerais, Brazil. This facility possesses three points of release of liquid effluents containing radionuclides: point 014, 025 and 076. At these points, the values of activity concentrations (AC) of the radionuclides U{sub nat}, {sup 226}Ra, {sup 210}Pb, {sup 232}Th and {sup 228}Ra were analyzed in 2012. The evaluation of point 014 by univariate statistics pointed four groups. [U{sub nat} > {sup 228}Ra > ({sup 226}Ra = {sup 210}Pb) >{sup 232}Th]. The multivariate statistics separated the radionuclides into two groups: [(U{sub nat} and {sup 232}Th) and ({sup 226}Ra, {sup 228}Ra and {sup 210}Pb)]. At point 025, the univariate statistics described three groups: [Un{sub at} > ({sup 228}Ra = {sup 210}Pb) > ({sup 226}Ra = {sup 232}Th)] and the multivariate analysis also described three but different groups: [(U{sub nat} and {sup 228}Ra), ({sup 226}Ra and {sup 210}Pb) and {sup 232}Th]. In turn, point 076 showed another behavior. The univariate analysis showed only two groups: [(U{sub nat}) > ({sup 226}Ra, {sup 228}Ra, {sup 210}Pb, {sup 232}Th)]. Differently, the multivariate statistics defined three groups: [(U{sub nat} and {sup 232}Th), ({sup 226}Ra and {sup 228}Ra) and {sup 210}Pb].Thus, statistical analysis showed that each point has releases of effluents with different characteristics. Both the behaviors of releases, based on multivariate statistics, and of the AC magnitudes, based on the univariate statistics, are different between the points. The only common features were the greater magnitude of uranium and the smaller magnitude of thorium. (author)

  8. Biomedical and environmental aspects of the thorium fuel cycle: a selected, annotated bibliography

    Energy Technology Data Exchange (ETDEWEB)

    Faust, R.A.; Fore, C.S.; Cone, M.V.; Meyer, H.R.; Till, J.E.

    1979-07-01

    This bibliography was compiled to assist in the evaluation of the health and environmental consequences of high specific activity thorium and related nuclides which could be released to the environment by activities related to the Thorium Fuel Cycle. The general scope covers studies regarding potential releases, environmental transport, metabolism, dosimetry, dose assessment, and overall risk assessment for radionuclides specific to the NASAP project. This publication of 740 abstracted references highlights the biological and medical aspects of thorium 228 and thorium 232 in man and animals. Similar studies on related nuclides such as radium 224, radium 226, radium 228, and thorium 230 are also emphasized. Additional categories relevant to these radionuclides are included as follows: chemical analysis; ecological aspects; energy; geological aspects; instrumentation; legal and political aspects; monitoring, measurement and analysis; physical aspects; production; radiation safety and control; and waste disposal and management. Environmental assessment and sources categories were used for entries which contain a multiple use of categories. Leading authors appear alphabetically within each category. Indexes are provided for : author(s), geographic location, keywords, title, and publication description. The bibliography contains literature dating from December 1925 to February 1978.

  9. Pollution of the stream waters and sediments associated with the Crucea uranium mine (East Carpathians, Romania)

    Science.gov (United States)

    Petrescu, L.; Bilal, E.; Iatan, E. L.

    2009-04-01

    Uranium and thorium are omnipresent in our environment. Various anthropogenic activities involving the processing or use of materials rich in uranium may modify the natural abundance of uranium in water. The study is related to uranium mineralization located within Crucea ore deposit, in the East Carpathians, Romania. The Crucea uranium ore deposit is located in the eastern part of the Bistrita Mountains (40 Km southeast of the town of Vatra Dornei) in the headwaters of Crucea, Lesu and Livezi valleys. At present, this is the largest uranium mine in the country. In the past, the mining area covered 18 km2, but was gradually overtaken by logging activities. The exploration and mining facilities include thirty-two galleries, situated between 780 and 1040 m above sea level. Radioactive waste resulted from mining are disposed next to the mining facilities. The waste rock was disposed in piles of variable size that are spread over an area of 364,000 m2. Older dumps (18) have been already naturally reclaimed by forest vegetation. The vegetation cover played an important role in stabilizing the waste dump cover and in slowing down the uranium migration processes. A number of 46 water samples were taken in order to evaluate the impact of ore deposit (including its exploitation process) on the chemical composition of waters down to the exploitation galleries. The sediment samples were collected at 16 sampling points from the bottom of the studied stream waters. ICP-OES, XRF and IC methods was used to evaluate the impact of uranium mine dumps on the surface waters from Crucea region. According to the analytical data the stream waters showed a Ca - carbonate character. In relation to salinity, the pH and the anion NO3-, CO32-and SO42- contents display generally non-linear relationships with chloride. Uranium is the most significant trace element in the river waters nearby the waste rock dumps, sometimes reaching levels up to 1-mgṡL-1, well in excess of the Romanian

  10. Study of the 'Impatiens walleriana' for phytoremediation of chromium, thorium, uranium and zinc soil contamination

    Energy Technology Data Exchange (ETDEWEB)

    Torrecilha, Jefferson K.; Mariano, Gabriela P.; Silva, Paulo S.C. da, E-mail: jeffkoy@usp.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2013-07-01

    The objective of this study was to determine the Cr, Th, U and Zn transfer from soil to Impatiens walleriana and verify if this plant species is suitable for soil decontamination. Samples of small, medium and large size of the plant were collected in three different locations, University of Sao Paulo, IPEN and Cotia, as well as soil samples from the surroundings. Instrumental neutron activation analysis was applied to determine the element concentrations. Roots, stems and leaves of the plant samples were analyzed in separate in order to verify the preferential site of concentration of these elements in the plant. For the analyses, samples of the soil and the plants were dried and pulverized into a fine powder, accurately weighed and sealed in polyethylene bags, irradiated together with reference standard materials in the IEA-R1 IPEN reactor and counted in a Ge-hiperpure detector. Cr, Th, and U did not present a significant potential to be accumulated in none of the plant parts. Zinc, on the other hand, showed great capacity to be accumulated in in all parts of Impatiens walleriana and, therefore, this species is a good candidate to be used for phytoremediation purpose, in case of soil contamination with zinc. (author)

  11. An analytical method to determine activity concentrations of uranium- and thorium-series radionuclides in outdoor air

    Energy Technology Data Exchange (ETDEWEB)

    Rozas, S.; Moja, M.; Alegria, N.; Idoeta, R.; Herranz, M. [Department of Nuclear Engineering and Fluid Mechanics, University of the Basque Country (UPV/EHU), Alameda Urquijo s/n, E-48013, Bilbao (Spain)

    2014-07-01

    Radon and its progeny in the outdoor air are one of the contributors to human exposure from natural sources. However, not only are their concentrations in the low layers of the atmosphere very low and affected by atmospheric mixing phenomena, some of these radionuclides have quite a low or very low half-life as well. These facts make the assessment of an independent activity concentration value for each of them difficult and as the existence of radioactive equilibrium in free air among the different radionuclides from the radioactive series cannot be considered, some approaches like the use of an established equilibrium factor are usually taken into account. Therefore, the objectives of this study are to characterize the outdoor air of Bilbao (Spain) in terms of natural radionuclides composition and to obtain the specific value of the equilibrium factor between radon and its progeny. To achieve these objectives a set of experimental steps have been carried out: aerosols and particles have been collected from the air using an aerosol sampling station with a nominal flow rate of 500 m{sup 3} h{sup -1} and, simultaneously, the Rn activity concentration was obtained by means of an automatic radon probe which provides values applying a pseudo-coincidence technique. Obtained particle filters were immediately measured by gamma-ray spectrometry and also one week and one month after the first measurement. After that, an analytical method, based on Bateman equations, has been used to obtain the activity concentrations of short-lived radionuclides in the sampled air from the values obtained in the early gamma-ray measurements. This analytical method has been previously used to determine the activity concentration of these radionuclides during a welding process and results have been published. As a result of this process, the air is characterized and the data needed to assess the equilibrium factor, by means of the equilibrium equivalent radon concentration, obtained. Achieved results show that activity concentration mean values are close to the values reported by UNSCEAR, being: 1.5 ± 0.1 μBq m{sup -3} of {sup 238}U, 3.0 ± 0.8 μBq m{sup -3} of {sup 226}Ra, 2.2 ± 0.1 Bq m{sup -3} of {sup 218}Po, {sup 214}Pb and {sup 214}Bi, 0.36 ± 0.05 mBq m{sup -3} of {sup 210}Pb, 1.8 ± 0.1 μBq m{sup -3} of {sup 228}Ra, 1.41 ± 0.04 μBq m{sup -3} of {sup 228}Th, 1.51 ± 0.04 μBq m{sup -3} of {sup 228}Ra and 0.022 ± 0.011 Bq m{sup -3} of {sup 212}Pb and {sup 212}Bi. Besides, obtained equilibrium factor between radon and its progeny has a mean value of 0.24. This value matches other values provided by the scientific literature. (authors)

  12. Coordination polymers of uranium(IV) terephthalates.

    Science.gov (United States)

    Falaise, Clément; Assen, Ayalew; Mihalcea, Ionut; Volkringer, Christophe; Mesbah, Adel; Dacheux, Nicolas; Loiseau, Thierry

    2015-02-14

    A series of tetravalent uranium terephthalates has been solvothermally synthesized in the solvent N,N-dimethylformamide (DMF) at temperature 100-150 °C with different water amounts. Composition diagrams have been determined for the U(4+) metallic cation in the presence of terephthalic acid, and their crystal structures revealed the occurrence of two- or three-dimensional coordination polymers. In the absence of water, a mixture of two polytypes T-U(2)Cl(2)(bdc)(3)(DMF)(4) (1) and M-U(2)Cl(2)(bdc)(3)(DMF)(4) (2) has been identified at low temperature (100-110 °C) for bdc/U = 1-4 (bdc = terephthalate linker). Their structures are built up from isolated uranium centers in nine-fold coordination, surrounded by 6 carboxyl oxygen atoms, 2 oxygen atoms coming from DMF molecules and one chlorine atom. The uranium cations are linked to each other through the bdc ligand in order to generate a 3D framework. By increasing the temperature (130-150 °C), a layered like compound has been isolated, U(2)(bdc)(4)(DMF)(4) (3). It is composed of discrete actinide centers in ten-fold coordination, with 8 carboxyl oxygen atoms and 2 oxygen atoms from DMF molecules. The connection of the UO10 units with the bdc linkers generates 2D sheets. When a controlled amount of water is added to the reaction medium, the crystallization of the UiO-66-like U(6)O(4)(OH)(4)(H(2)O)(6)(bdc)(6)·10DMF solid (containing a hexanuclear sub-unit) is observed for temperature 110-120 °C and the H(2)O/U molar ratio in the range of 2-10. At higher temperature (140-150 °C), a distinct phase appeared, U(2)O(2)(bdc)(2)(DMF) (4), which consists of infinite chains of uranium centers, linked to each other via the bdc ligands. Higher water contents led to the formation of urania UO(2).

  13. Stabilization of Th 3+ ions into mixed-valence thorium fluoride

    Science.gov (United States)

    Dubois, Marc; Dieudonné, Belto; Mesbah, Adel; Bonnet, Pierre; El-Ghozzi, Malika; Renaudin, Guillaume; Avignant, Daniel

    2011-01-01

    The unusual oxidation state +3 of the thorium has been stabilized into a lithium containing non-stoichiometric mixed-valence (III/IV) thorium fluorinated phase with formula Li 2+ xTh 12F 50 (0afore mentioned single phase may be considered as an insertion compound. The Li + insertion is accompanied by the simultaneous reduction of a part of the Th 4+ ions, resulting in a mixed-valence III/IV thorium fluoride. The electrochemical insertion of Li + ions into the open channels of the host matrix has been carried out at 60 °C, using an alkylcarbonate PC-LiClO 4 1 M electrolyte. The Li + and Th 3+ contents, both in the starting composition and the Li + inserted ones, were investigated by high resolution solid state 7Li NMR and EPR, respectively.

  14. Thorium-230 Stratigraphy of Alpha Ridge Sediment (Arctic Ocean)

    Science.gov (United States)

    Not, C.; Hillaire-Marcel, C.; Polyak, L.; Darby, D.

    2006-12-01

    The Alpha Ridge (central Arctic Ocean) is characterized by very uniform sedimentary deposition essentially linked to vertical particulate rain. This property led us to investigate the behavior of U-series isotopes (Th-230 and Pb-210) in such a setting, i.e., one without significant sedimentary advection. Two sites cored with a 70 cm-long multicorer during the 2005 Hotrax Expedition and located about 20 nautical miles apart and at different water depths (core 11: 2644 m and core 12: 1585 m) were selected for the purpose of this study. Lead-210 profiles are practically identical in both cores, with high activities at the surface (>30 dpm/g), followed by a first minimum at 1 cm (depth. This pattern suggests significant bioturbation, at least down to 8-10 cm, and some Pb-210 diffusion below. At three distinct depths the Th-230 activities are above supported Th-230 values (approx. 1.2 dpm/g): from 0 to 8 cm (with a maximum ranging 25-30 dpm/g), 15 to 20 cm (up to 7 dpm/g) and 26 cm to core bottom (34 and 38 cm, respectively in cores 12 and 11). Here again, despite their large bathymetric difference, the two sites yielded almost identical 230Th-profiles. 230Th-activities are highly correlated with the CaCO3 content, allowing for the decay of the excess-thorium 230 (230Thxs) downcore. Assuming a linear initial relationship between CaCO3 and Th-230xs, the assignment of the lowermost part (below 37 cm) of core 11 to the oxygen isotope 5e seems probable. Maximums in organic carbon and carbonate contents at the base and top of the cores would support this interpretation. In such settings, Th-230 reveals useful data to constrain the stratigraphy of the late Pleistocene sediments, and may compensate for the absence of a viable oxygen isotope stratigraphy.

  15. Measurement of radium and thorium isotopes in environmental samples by alpha-spectrometry

    OpenAIRE

    Rodríguez Álvarez, María José; Sánchez, F.

    1995-01-01

    The final publication is available at Springer via http://dx.doi.org/10.1007/BF02035979 A new method for the determination of low-level radium and thorium isotopes in environmental samples by α-spectrometry is described. Thorium and radium isotopes were chemically separated from the same sample, by using the same tracer (229Th). Two different ways were explored for the concentration process in water samples, obtaining a chemical yield for Ra isotopes between 70–90% in both cases using KMnO...

  16. Uranium favourability study in Nigeria

    Science.gov (United States)

    Oshin, I. O.; Rahaman, M. A.

    Geological considerations indicate that four types of uranium deposits, three from within the crystalline rocks and the fourth from the sedimentary formations, can be explored for in Nigeria. The Precambrian Basement Complex underwent crustal reactivation in Pan-African times (600 ± 150 Ma) during which migmatites and rocks of the Older Granite suite were emplaced. The occurrences of these rocks in northeastern, north-central and central Nigeria are possible hosts for the granitic type of uranium deposit. Vein-type uranium deposits are often localized in areas of the Basement Complex which have undergone intense brittle deformation. The high-level, anorogenic, peralkaline Younger Granites of Nigeria of Carboniferous to Cretaceous age have geochemical characteristics which are similar to those of the host rocks of non-orogenic type uranium deposit in alkali complexes such as the Bokan mountains of Alaska. The sandstone type of uranium deposit may be found in the Cretaceous-Recent continental sandstone formations in the Sokoto, Niger, Chad and Benue Basins of Nigeria and in the sediments overlying the Oban Massif in Cross Rivers State. Geologically similar sandstone occurrences elsewhere in the world (Gabon, Niger and Colorado, U.S.A.) are known to harbour important uranium mineralization.

  17. Uranium uptake by hydroponically cultivated crop plants

    Energy Technology Data Exchange (ETDEWEB)

    Soudek, Petr; Petrova, Sarka [Laboratory of Plant Biotechnologies, Joint Laboratory of Institute of Experimental Botany AS CR, v.v.i. and Crop Research Institute, v.v.i., Rozvojova 263, 162 05 Prague 6 (Czech Republic); Benesova, Dagmar [Laboratory of Plant Biotechnologies, Joint Laboratory of Institute of Experimental Botany AS CR, v.v.i. and Crop Research Institute, v.v.i., Rozvojova 263, 162 05 Prague 6 (Czech Republic); Faculty of Environment Technology, Institute of Chemical Technology, Technicka 5, 166 28 Prague 6 (Czech Republic); Dvorakova, Marcela [Laboratory of Plant Biotechnologies, Joint Laboratory of Institute of Experimental Botany AS CR, v.v.i. and Crop Research Institute, v.v.i., Rozvojova 263, 162 05 Prague 6 (Czech Republic); Vanek, Tomas, E-mail: vanek@ueb.cas.cz [Laboratory of Plant Biotechnologies, Joint Laboratory of Institute of Experimental Botany AS CR, v.v.i. and Crop Research Institute, v.v.i., Rozvojova 263, 162 05 Prague 6 (Czech Republic)

    2011-06-15

    Hydroponicaly cultivated plants were grown on medium containing uranium. The appropriate concentrations of uranium for the experiments were selected on the basis of a standard ecotoxicity test. The most sensitive plant species was determined to be Lactuca sativa with an EC{sub 50} value about 0.1 mM. Cucumis sativa represented the most resistant plant to uranium (EC{sub 50} = 0.71 mM). Therefore, we used the uranium in a concentration range from 0.1 to 1 mM. Twenty different plant species were tested in hydroponic solution supplemented by 0.1 mM or 0.5 mM uranium concentration. The uranium accumulation of these plants varied from 0.16 mg/g DW to 0.011 mg/g DW. The highest uranium uptake was determined for Zea mays and the lowest for Arabidopsis thaliana. The amount of accumulated uranium was strongly influenced by uranium concentration in the cultivation medium. Autoradiography showed that uranium is mainly localized in the root system of the plants tested. Additional experiments demonstrated the possibility of influencing the uranium uptake from the cultivation medium by amendments. Tartaric acid was able to increase uranium uptake by Brassica oleracea and Sinapis alba up to 2.8 times or 1.9 times, respectively. Phosphate deficiency increased uranium uptake up to 4.5 times or 3.9 times, respectively, by Brassica oleracea and S. alba. In the case of deficiency of iron or presence of cadmium ions we did not find any increase in uranium accumulation. - Highlights: > The uranium accumulation in twenty different plant species varied from 0.160 to 0.011 mg/g DW. > Uranium is mainly localized in the root system. > Tartaric acid was able to increase uranium uptake by Brassica oleracea and Sinapis alba. > The phosphates deficiency increase the uranium uptake.

  18. Microbial accumulation of uranium, radium, and cesium

    Energy Technology Data Exchange (ETDEWEB)

    Strandberg, G.W.; Shumate, S.E. II; Parrott, J.R. Jr.; North, S.E.

    1981-05-01

    Diverse microbial species varied considerably in their ability to accumulate uranium, cesium, and radium. Mechanistic differences in uranium uptake by Saccharomyces cerevisiae and Pseudomonas aeruginosa were indicated. S. serevisiae exhibited a slow (hours) surface accumulation of uranium which was subject to environmental factors, while P. aeruginosa accumulated uranium rapidly (minutes) as dense intracellular deposits and did not appear to be affected by environmental parameters. Metabolism was not required for uranium uptake by either organism. Cesium and radium were concentrated to a considerably lesser extent than uranium by the several species tested.

  19. SOLVENT EXTRACTION PROCESS FOR URANIUM RECOVERY

    Science.gov (United States)

    Clark, H.M.; Duffey, D.

    1958-06-17

    A process is described for extracting uranium from uranium ore, wherein the uranium is substantially free from molybdenum contamination. In a solvent extraction process for recovering uranium, uranium and molybdenum ions are extracted from the ore with ether under high acidity conditions. The ether phase is then stripped with water at a lower controiled acidity, resaturated with salting materials such as sodium nitrate, and reextracted with the separation of the molybdenum from the uranium without interference from other metals that have been previously extracted.

  20. Optimization of Uranium Molecular Deposition for Alpha-Counting Sources

    Energy Technology Data Exchange (ETDEWEB)

    Monzo, Ellen [Univ. of Minnesota, Duluth, MN (United States); Parsons-Moss, Tashi [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Genetti, Victoria [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Knight, Kimberly [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2016-12-12

    Method development for molecular deposition of uranium onto aluminum 1100 plates was conducted with custom plating cells at Lawrence Livermore National Laboratory. The method development focused primarily on variation of electrode type, which was expected to directly influence plated sample homogeneity. Solid disc platinum and mesh platinum anodes were compared and data revealed that solid disc platinum anodes produced more homogenous uranium oxide films. However, the activity distribution also depended on the orientation of the platinum electrode relative to the aluminum cathode, starting current, and material composition of the plating cell. Experiments demonstrated these variables were difficult to control under the conditions available. Variation of plating parameters among a series of ten deposited plates yielded variations up to 30% in deposition efficiency. Teflon particles were observed on samples plated in Teflon cells, which poses a problem for alpha activity measurements of the plates. Preliminary electropolishing and chemical polishing studies were also conducted on the aluminum 1100 cathode plates.

  1. Two novel thorium organic frameworks constructed by bi- and tritopic ligands

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Fei [National Institute for Radiological Protection, Beijing (China). China CDC Key Lab. of Radiological Pretection and Nuclear Emergency; Chinese Academy of Sciences, Beijing (China). Inst. of High Energy Physics; Wang, Congzhi; Lan, Jianhui; Chai, Zhifang [Chinese Academy of Sciences, Beijing (China). Inst. of High Energy Physics; Ji, Yanqin [National Institute for Radiological Protection, Beijing (China). China CDC Key Lab. of Radiological Pretection and Nuclear Emergency

    2017-09-01

    Two thorium organic frameworks, Th(BDC){sub 2} and Th(OH)(BCPBA) have been hydrothermally synthesized using 1,4-benzenedicarboxylic acid (H{sub 2}BDC) and 3,5-bi(4-carboxyphenoxy)benzoic acid (H{sub 3}BCPBA), respectively. The obtained two compounds were determined by single-crystal XRD, and they exhibited two new topologies. Th(BDC){sub 2} shows a 3-dimensional (4,4,8)-connected framework with the Schlaefli symbol of (4{sup 14}.6{sup 12}.8{sup 2})(4{sup 2}.6{sup 3}.8)(4{sup 4}.6{sup 2}), and it is a mononuclear thorium(IV) complex. Th(OH)(BCPBA) possesses a (4,6)-connected topology with the Schlaefli symbol of (4{sup 15}){sup 2}(4{sup 6}){sup 3}, and it has a dinuclear thorium(IV) asymmetric unit with the shortest Th-Th distances. Viewing along suitable directions, channels with different shapes can be found in the obtained two frameworks. Based on calculation with PLATON, the amount of void space is 21.9% and 13.5% in Th(BDC){sub 2} and Th(OH)(BCPBA), respectively. Density functional theory (DFT) studies revealed that the metal-ligand interactions were mainly of ionic character in both compounds and the hydroxyl ions might play an important role in the stability of dinuclear thorium(IV) of Th(OH)(BCPBA).

  2. Application of hollow cylindrical wheat stem for electromembrane extraction of thorium in water samples

    DEFF Research Database (Denmark)

    Khajeh, Mostafa; Pedersen-Bjergaard, Stig; Barkhordar, Afsaneh

    2015-01-01

    In this study, wheat stem was used for electromembrane extraction (EME) for the first time. The EME technique involved the use of a wheat stem whose channel was filled with 3 M HCl, immersed in 10 mL of an aqueous sample solution. Thorium migrated from aqueous samples, through a thin layer of 1...

  3. Page 1 Gravimetric Determination of Thorium 239 done in the pH ...

    Indian Academy of Sciences (India)

    The thorium content of the solution was determined by the 8-hydroxy-quinoline method. (b) 1-hydroxy-3-methoxy Xanthone.--It was prepared by the condensa- tion of phloroglucinol-dimethyl ether' with salicylic acid in presence of fused zinc chloride. A 2% (almost Saturated) solution of the xanthone in alcohol was used.

  4. Evaluation of the level of thorium in Yargalma gold ore by x-ray ...

    African Journals Online (AJOL)

    The analytical study for the first time has provided a baseline data on the level of thorium and other elemental composition in Yargalma gold ore, a baseline information on the anthropogenic impact of environmental pollution in the mining community and the basis for planning management strategy to achieve better ...

  5. Extração líquido-líquido de urânio(VI do colofanito de itataia (Santa Quitéria, Ceará por extratantes orgânicos em presença de ácido fosfórico Liquid-liquid extraction of uranium(VI from colofanite of itataia (Santa Quitéria, Ceará by organic extractants in the presence of phosphoric acid

    Directory of Open Access Journals (Sweden)

    Valeria Aparecida Leitão Ribeiro

    2008-01-01

    Full Text Available This work describes the liquid-liquid extraction of uranium after digestion of colofanite (a fluoroapatite from Itataia with sulfuric acid. The experiments were run at room temperature in one stage. Among the solutions tested the highest distribution coefficient (D > 60 was found for 40%vol. DEHPA (di(2-ethyl-hexylphosphoric acid + 20% vol. TOPO (trioctylphosphine oxide in kerosene. Thorium in the raffinate was quantitatively extracted by TOPO (0.1% vol. in cyclohexane. Uranium stripping and separation from iron was possible using 1.5 mol L-1 ammonium or sodium carbonate (room temperature, one stage. However, pH control is essential for a good separation.

  6. Development of uranium waste management concept

    Energy Technology Data Exchange (ETDEWEB)

    Yamamoto, Masafumi [Research Division of LLW Disposal System, Radioactive Waste Management Funding and Research Center (RWMC), Tokyo (Japan)

    2001-02-01

    The Japanese long-term program for nuclear energy development and utilization issued in 2000 says that a considerable fraction of uranium wastes can be disposed using shallow underground facilities by controlling uranium concentration in the uranium wastes and by adopting the allowable exposure dose not exceeding 0.1 mSv per year. The present report gives an estimate on the total amount of uranium wastes currently generated in Japan and its future prospect. Uranium wastes whose uranium concentration range from 10{sup 6} Bq/t to 10{sup 10} Bq/t are generated from nuclear facilities, such as fuel cycle (JNC), fuel fabricating, and uranium enrichment facilities. Stress is put on uranium recovery (decontamination) process and various anticipated techniques of waste disposals depending on their generation sources are briefly discussed. (S. Ohno)

  7. Variations in the uranium isotopic compositions of uranium ores from different types of uranium deposits

    Science.gov (United States)

    Uvarova, Yulia A.; Kyser, T. Kurt; Geagea, Majdi Lahd; Chipley, Don

    2014-12-01

    Variations in 238U/235U and 234U/238U ratios were measured in uranium minerals from a spectrum of uranium deposit types, as well as diagenetic phosphates in uranium-rich basins and peraluminous rhyolites and associated autunite mineralisation from Macusani Meseta, Peru. Mean δ238U values of uranium minerals relative to NBL CRM 112-A are 0.02‰ for metasomatic deposits, 0.16‰ for intrusive, 0.18‰ for calcrete, 0.18‰ for volcanic, 0.29‰ for quartz-pebble conglomerate, 0.29‰ for sandstone-hosted, 0.44‰ for unconformity-type, and 0.56‰ for vein, with a total range in δ238U values from -0.30‰ to 1.52‰. Uranium mineralisation associated with igneous systems, including low-temperature calcretes that are sourced from U-rich minerals in igneous systems, have low δ238U values of ca. 0.1‰, near those of their igneous sources, whereas uranium minerals in basin-hosted deposits have higher and more variable values. High-grade unconformity-related deposits have δ238U values around 0.2‰, whereas lower grade unconformity-type deposits in the Athabasca, Kombolgie and Otish basins have higher δ238U values. The δ234U values for most samples are around 0‰, in secular equilibrium, but some samples have δ234U values much lower or higher than 0‰ associated with addition or removal of 234U during the past 2.5 Ma. These δ238U and δ234U values suggest that there are at least two different mechanisms responsible for 238U/235U and 234U/238U variations. The 234U/238U disequilibria ratios indicate recent fluid interaction with the uranium minerals and preferential migration of 234U. Fractionation between 235U and 238U is a result of nuclear-field effects with enrichment of 238U in the reduced insoluble species (mostly UO2) and 235U in oxidised mobile species as uranyl ion, UO22+, and its complexes. Therefore, isotopic fractionation effects should be reflected in 238U/235U ratios in uranium ore minerals formed either by reduction of uranium to UO2 or chemical

  8. Uranium briquettes for irradiation target

    Energy Technology Data Exchange (ETDEWEB)

    Saliba-Silva, Adonis Marcelo; Garcia, Rafael Henrique Lazzari; Martins, Ilson Carlos; Carvalho, Elita Fontenele Urano de; Durazzo, Michelangelo, E-mail: saliba@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2011-07-01

    Direct irradiation on targets inside nuclear research or multiple purpose reactors is a common route to produce {sup 99}Mo-{sup 99m}Tc radioisotopes. Nevertheless, since the imposed limits to use LEU uranium to prevent nuclear armament production, the amount of uranium loaded in target meats has physically increased and new processes have been proposed for production. Routes using metallic uranium thin film and UAl{sub x} dispersion have been used for this purpose. Both routes have their own issues, either by bringing difficulties to disassemble the aluminum case inside hot cells or by generating great amount of alkaline radioactive liquid rejects. A potential route might be the dispersion of powders of LEU metallic uranium and nickel, which are pressed as a blend inside a die and followed by pulse electroplating of nickel. The electroplating provides more strength to the briquettes and creates a barrier for gas evolution during neutronic disintegration of {sup 235}U. A target briquette platted with nickel encapsulated in an aluminum case to be irradiated may be an alternative possibility to replace other proposed targets. This work uses pulse Ni-electroplating over iron powder briquette to simulate the covering of uranium by nickel. The following parameters were applied 10 times for each sample: 900Hz, -0.84A/square centimeters with duty cycle of 0.1 in Watts Bath. It also presented the optical microscopy analysis of plated microstructure section. (author)

  9. Comparison for thorium fuel cycle facilities of two different capacities for implementation of safeguards

    Energy Technology Data Exchange (ETDEWEB)

    Gangotra, Suresh, E-mail: sgangotra@yahoo.co.in; Grover, R.B.; Ramakumar, K.L.

    2013-09-15

    Highlights: • Facilities for implementation of safeguards for thorium fuel cycle have been compared. • Two concepts have been compared. • In one concept, the facilities are designed in hub and spoke concept. • In second concept the facilities are designed as self-contained concept. • The comparison is done on a number of factors, which affect safeguardability and proliferation resistance. -- Abstract: Thorium based nuclear fuel cycle has many attractive features, its inherent proliferation resistance being one of them. This is due to the presence of high energy gamma emitting daughter products of U{sup 232} associated with U{sup 233}. This high energy gamma radiation also poses challenges in nuclear material accounting. A typical thorium fuel cycle facility has a number of plants including a fuel fabrication plant for initial and equilibrium core, a reprocessed U{sup 233} fuel fabrication plant, a reprocessing plant, a fuel assembly/disassembly plant and associated waste handling and management plants. A thorium fuel cycle facility can be set up to serve reactors at a site. Alternatively, one can follow a hub and spoke approach with a large thorium fuel cycle facility acting as a hub, catering to the requirements of reactors at several sites as spokes. These two concepts have their respective merits and shortcomings in terms of engineering and economics. The present paper is aimed at comparing the merits and challenges for implementation of safeguards on the two concepts viz. a large fuel cycle hub catering to reactors at several sites versus a small fuel cycle facility dedicated to reactors at a single site.

  10. RECOVERY OF URANIUM VALUES FROM URANIUM BEARING RAW MATERIALS

    Science.gov (United States)

    Michal, E.J.; Porter, R.R.

    1959-06-16

    Uranium leaching from ground uranium-bearing raw materials using MnO/sub 2/ in H/sub 2/SO/sub 4/ is described. The MnO/sub 2/ oxidizes U to the leachable hexavalent state. The MnO/sub 2/ does not replace Fe normally added, because the Fe complexes P and catalyzes the MnO/sub 2/ reaction. Three examples of continuous processes are given, but batch operation is also possible. The use of MnO/sub 2/ makes possible recovery of very low U values. (T.R.H.)

  11. Manhattan Project Technical Series The Chemistry of Uranium (I) Chapters 1-10

    Energy Technology Data Exchange (ETDEWEB)

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

    1946-09-30

    This constitutes Chapters 1 through 10. inclusive, of The Survey Volume on Uranium Chemistry prepared for the Manhattan Project Technical Series. Chapters are titled: Nuclear Properties of Uranium; Properties of the Uranium Atom; Uranium in Nature; Extraction of Uranium from Ores and Preparation of Uranium Metal; Physical Properties of Uranium Metal; Chemical Properties of Uranium Metal; Intermetallic Compounds and Alloy systems of Uranium; the Uranium-Hydrogen System; Uranium Borides, Carbides, and Silicides; Uranium Nitrides, Phosphides, Arsenides, and Antimonides.

  12. 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.)

  13. 77 FR 12880 - Uranium From Russia

    Science.gov (United States)

    2012-03-02

    ... COMMISSION Uranium From Russia Determination On the basis of the record \\1\\ developed in the subject five... investigation on uranium from Russia would be likely to lead to continuation or recurrence of material injury to... Publication 4307 (February 2012), entitled Uranium from Russia: Investigation No. 731-TA-539-C (Third Review...

  14. The Chemistry and Toxicology of Depleted Uranium

    Directory of Open Access Journals (Sweden)

    Sidney A. Katz

    2014-03-01

    Full Text Available Natural uranium is comprised of three radioactive isotopes: 238U, 235U, and 234U. Depleted uranium (DU is a byproduct of the processes for the enrichment of the naturally occurring 235U isotope. The world wide stock pile contains some 1½ million tons of depleted uranium. Some of it has been used to dilute weapons grade uranium (~90% 235U down to reactor grade uranium (~5% 235U, and some of it has been used for heavy tank armor and for the fabrication of armor-piercing bullets and missiles. Such weapons were used by the military in the Persian Gulf, the Balkans and elsewhere. The testing of depleted uranium weapons and their use in combat has resulted in environmental contamination and human exposure. Although the chemical and the toxicological behaviors of depleted uranium are essentially the same as those of natural uranium, the respective chemical forms and isotopic compositions in which they usually occur are different. The chemical and radiological toxicity of depleted uranium can injure biological systems. Normal functioning of the kidney, liver, lung, and heart can be adversely affected by depleted uranium intoxication. The focus of this review is on the chemical and toxicological properties of depleted and natural uranium and some of the possible consequences from long term, low dose exposure to depleted uranium in the environment.

  15. Monte Carlo studies of uranium calorimetry

    Energy Technology Data Exchange (ETDEWEB)

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

    1985-01-01

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

  16. Uranium phosphate biomineralization by fungi.

    Science.gov (United States)

    Liang, Xinjin; Hillier, Stephen; Pendlowski, Helen; Gray, Nia; Ceci, Andrea; Gadd, Geoffrey Michael

    2015-06-01

    Geoactive soil fungi were investigated for phosphatase-mediated uranium precipitation during growth on an organic phosphorus source. Aspergillus niger and Paecilomyces javanicus were grown on modified Czapek-Dox medium amended with glycerol 2-phosphate (G2P) as sole P source and uranium nitrate. Both organisms showed reduced growth on uranium-containing media but were able to extensively precipitate uranium and phosphorus-containing minerals on hyphal surfaces, and these were identified by X-ray powder diffraction as uranyl phosphate species, including potassium uranyl phosphate hydrate (KPUO6 .3H2 O), meta-ankoleite [(K1.7 Ba0.2 )(UO2 )2 (PO4 )2 .6H2 O], uranyl phosphate hydrate [(UO2 )3 (PO4 )2 .4H2 O], meta-ankoleite (K(UO2 )(PO4 ).3H2 O), uramphite (NH4 UO2 PO4 .3H2 O) and chernikovite [(H3 O)2 (UO2 )2 (PO4 )2 .6H2 O]. Some minerals with a morphology similar to bacterial hydrogen uranyl phosphate were detected on A. niger biomass. Geochemical modelling confirmed the complexity of uranium speciation, and the presence of meta-ankoleite, uramphite and uranyl phosphate hydrate between pH 3 and 8 closely matched the experimental data, with potassium as the dominant cation. We have therefore demonstrated that fungi can precipitate U-containing phosphate biominerals when grown with an organic source of P, with the hyphal matrix serving to localize the resultant uranium minerals. The findings throw further light on potential fungal roles in U and P biogeochemistry as well as the application of these mechanisms for element recovery or bioremediation. © 2015 Society for Applied Microbiology and John Wiley & Sons Ltd.

  17. Influence of terrestrial radionuclides on environmental gamma exposure in a uranium deposit in Paraíba, Brazil.

    Science.gov (United States)

    Araújo Dos Santos Júnior, José; Dos Santos Amaral, Romilton; Simões Cezar Menezes, Rômulo; Reinaldo Estevez Álvarez, Juan; Marques do Nascimento Santos, Josineide; Herrero Fernández, Zahily; Dias Bezerra, Jairo; Antônio da Silva, Alberto; Francys Rodrigues Damascena, Kennedy; de Almeida Maciel Neto, José

    2017-07-01

    One of the main natural uranium deposits in Brazil is located in the municipality of Espinharas, in the State of Paraíba. This area may present high levels of natural radioactivity due to the presence of these radionuclides. Since this is a populated area, there is need for a radioecological dosimetry assessment to investigate the possible risks to the population. Based on this problem, the objective of this study was to estimate the environmental effective dose outdoors in inhabited areas influenced by the uranium deposit, using the specific activities of equivalent uranium, equivalent thorium and 40K and conversion factors. The environmental assessment was carried using gamma spectroscopy in sixty-two points within the municipality, with a high-resolution gamma spectrometer with HPGe semiconductor detector and Be window. The results obtained ranged from 0.01 to 19.11 mSv y-1, with an average of 2.64 mSv y-1. These levels are, on average, 23 times higher than UNSCEAR reference levels and up to 273 times the reference value of the earth's crust for primordial radionuclides. Therefore, given the high radioactivity levels found, we conclude that there is need for further investigation to evaluate the levels of radioactivity in indoor environments, which will reflect more closely the risks of the local population. Copyright © 2017 Elsevier Inc. All rights reserved.

  18. Release behavior of uranium in uranium mill tailings under environmental conditions.

    Science.gov (United States)

    Liu, Bo; Peng, Tongjiang; Sun, Hongjuan; Yue, Huanjuan

    2017-05-01

    Uranium contamination is observed in sedimentary geochemical environments, but the geochemical and mineralogical processes that control uranium release from sediment are not fully appreciated. Identification of how sediments and water influence the release and migration of uranium is critical to improve the prevention of uranium contamination in soil and groundwater. To understand the process of uranium release and migration from uranium mill tailings under water chemistry conditions, uranium mill tailing samples from northwest China were investigated with batch leaching experiments. Results showed that water played an important role in uranium release from the tailing minerals. The uranium release was clearly influenced by contact time, liquid-solid ratio, particle size, and pH under water chemistry conditions. Longer contact time, higher liquid content, and extreme pH were all not conducive to the stabilization of uranium and accelerated the uranium release from the tailing mineral to the solution. The values of pH were found to significantly influence the extent and mechanisms of uranium release from minerals to water. Uranium release was monitored by a number of interactive processes, including dissolution of uranium-bearing minerals, uranium desorption from mineral surfaces, and formation of aqueous uranium complexes. Considering the impact of contact time, liquid-solid ratio, particle size, and pH on uranium release from uranium mill tailings, reducing the water content, decreasing the porosity of tailing dumps and controlling the pH of tailings were the key factors for prevention and management of environmental pollution in areas near uranium mines. Copyright © 2017 Elsevier Ltd. All rights reserved.

  19. Radioactive mineral spring precipitates, their analytical and statistical data and the uranium connection

    Science.gov (United States)

    Cadigan, R.A.; Felmlee, J.K.

    1982-01-01

    Major radioactive mineral springs are probably related to deep zones of active metamorphism in areas of orogenic tectonism. The most common precipitate is travertine, a chemically precipitated rock composed chiefly of calcium carbonate, but also containing other minerals. The mineral springs are surface manifestations of hydrothermal conduit systems which extend downward many kilometers to hot source rocks. Conduits are kept open by fluid pressure exerted by carbon dioxide-charged waters rising to the surface propelled by heat and gas (CO2 and steam) pressure. On reaching the surface, the dissolved carbon dioxide is released from solution, and calcium carbonate is precipitated. Springs also contain sulfur species (for example, H2S and HS-), and radon, helium and methane as entrained or dissolved gases. The HS- ion can react to form hydrogen sulfide gas, sulfate salts, and native sulfur. Chemical salts and native sulfur precipitate at the surface. The sulfur may partly oxidize to produce detectable sulfur dioxide gas. Radioactivity is due to the presence of radium-226, radon-222, radium-228, and radon-220, and other daughter products of uranium-238 and thorium-232. Uranium and thorium are not present in economically significant amounts in most radioactive spring precipitates. Most radium is coprecipitated at the surface with barite. Barite (barium sulfate) forms in the barium-containing spring water as a product of the oxidation of sulfur species to sulfate ions. The relatively insoluble barium sulfate precipitates and removes much of the radium from solution. Radium coprecipitates to a lesser extent with manganese-barium- and iron-oxy hydroxides. R-mode factor analysis of abundances of elements suggests that 65 percent of the variance of the different elements is affected by seven factors interpreted as follows: (1) Silica and silicate contamination and precipitation; (2) Carbonate travertine precipitation; (3) Radium coprecipitation; (4) Evaporite precipitation

  20. The Chemistry and Toxicology of Depleted Uranium

    OpenAIRE

    Sidney A. Katz

    2014-01-01

    Natural uranium is comprised of three radioactive isotopes: 238U, 235U, and 234U. Depleted uranium (DU) is a byproduct of the processes for the enrichment of the naturally occurring 235U isotope. The world wide stock pile contains some 1½ million tons of depleted uranium. Some of it has been used to dilute weapons grade uranium (~90% 235U) down to reactor grade uranium (~5% 235U), and some of it has been used for heavy tank armor and for the fabrication of armor-piercing bullets and missiles....

  1. Uranium mill monitoring for natural fission reactors

    Energy Technology Data Exchange (ETDEWEB)

    Apt, K.E.

    1977-12-01

    Isotopic monitoring of the product stream from operating uranium mills is proposed for discovering other possible natural fission reactors; aspects of their occurrence and discovery are considered. Uranium mill operating characteristics are formulated in terms of the total uranium capacity, the uranium throughput, and the dilution half-time of the mill. The requirements for detection of milled reactor-zone uranium are expressed in terms of the dilution half-time and the sampling frequency. Detection of different amounts of reactor ore with varying degrees of /sup 235/U depletion is considered.

  2. Oxidation states of uranium in depleted uranium particles from Kuwait.

    Science.gov (United States)

    Salbu, B; Janssens, K; Lind, O C; Proost, K; Gijsels, L; Danesi, P R

    2005-01-01

    The oxidation states of uranium in depleted uranium (DU) particles were determined by synchrotron radiation based mu-XANES, applied to individual particles isolated from selected samples collected at different sites in Kuwait. Based on scanning electron microscopy with X-ray microanalysis prior to mu-XANES, DU particles ranging from submicrons to several hundred micrometers were observed. The median particle size depended on sources and sampling sites; small-sized particles (median 13 microm) were identified in swipes taken from the inside of DU penetrators holes in tanks and in sandy soil collected below DU penetrators, while larger particles (median 44 microm) were associated with fire in a DU ammunition storage facility. Furthermore, the (236)U/(235)U ratios obtained from accelerator mass spectrometry demonstrated that uranium in the DU particles originated from reprocessed fuel (about 10(-2) in DU from the ammunition facility, about 10(-3) for DU in swipes). Compared to well-defined standards, all investigated DU particles were oxidized. Uranium particles collected from swipes were characterized as UO(2), U(3)O(8) or a mixture of these oxidized forms, similar to that observed in DU affected areas in Kosovo. Uranium particles formed during fire in the DU ammunition facility were, however, present as oxidation state +5 and +6, with XANES spectra similar to solid uranyl standards. Environmental or health impact assessments for areas affected by DU munitions should therefore take into account the presence of respiratory UO(2), U(3)O(8) and even UO(3) particles, their corresponding weathering rates and the subsequent mobilisation of U from oxidized DU particles.

  3. Separation of Protactinium from Neutron Irradiated Thorium Oxide; Separacion de Protactinio de Oxido de Torio Irradiado con Neutrones

    Energy Technology Data Exchange (ETDEWEB)

    Dominguez, G.; Gutierrez, L.; Ropero, M.

    1983-07-01

    The chemical separation of thorium and protactinium can be carried out by leaching most of the last one, about 95%, with aqueous HF from neutron irradiated thorium oxide. This leaching reaction la highly favored by the transformation reaction of the ThO{sub 2} material into ThF{sub 4}. For both reactions, leaching and transformation, the reagents concentration, agitation speed and temperature influences were studied and the activation energies were found. (Author) 18 refs.

  4. Uranium hydrogeochemical and stream sediment reconnaissance data release for the Dubois NTMS Quadrangle, Idaho/Montana, including concentrations of forty-five additional elements

    Energy Technology Data Exchange (ETDEWEB)

    LaDelfe, C.M.

    1980-08-01

    Totals of 1024 water samples and 1600 sediment samples were collected from 1669 locations in the Dubois quadrangle. Water samples were taken at streams, springs, and wells; sediment samples were collected from streams and springs. All field and analytical data are presented for waters in Appendix I-A and for sediments in I-B. All elemental analyses were performed at the LASL. Water samples were initially analyzed for uranium by fluorometry. All water samples containing more than the upper detection limit of uranium were reanalyzed by delayed neutron counting. Sediments were analyzed for uranium and thorium as well as aluminum, antimony, arsenic, barium, beryllium, bismuth, cadmium, calcium, cerium, cesium, chlorine, chromium, cobalt, copper, dysprosium, europium, gold, hafnium, iron, lanthanum, lead, lithium, lutetium, magnesium, manganese, nickel, niobium, potassium rubidium, samarium, scandium, selenium, silver, sodium, strontium, tantalum, terbium, tin, titanium, tungsten, vanadium, ytterbium, zinc and zirconium. All sediments were analyzed for uranium by delayed-neutron counting. Other elemental concentrations in sediments were determined by neutron-activation analysis for 30 elements, by x-ray fluorescence for 12 elements, and by arc-source emission spectrography for 2 elements. Analytical results for sediments are reported as parts per million.

  5. Uranium 2011 resources, production and demand

    CERN Document Server

    Organisation for Economic Cooperation and Development. Paris

    2012-01-01

    In the wake of the Fukushima Daiichi nuclear power plant accident, questions are being raised about the future of the uranium market, including as regards the number of reactors expected to be built in the coming years, the amount of uranium required to meet forward demand, the adequacy of identified uranium resources to meet that demand and the ability of the sector to meet reactor requirements in a challenging investment climate. This 24th edition of the “Red Book”, a recognised world reference on uranium jointly prepared by the OECD Nuclear Energy Agency and the International Atomic Energy Agency, provides analyses and information from 42 producing and consuming countries in order to address these and other questions. It offers a comprehensive review of world uranium supply and demand as well as data on global uranium exploration, resources, production and reactor-related requirements. It also provides substantive new information on established uranium production centres around the world and in countri...

  6. Uranium 2014 resources, production and demand

    CERN Document Server

    Organisation for Economic Cooperation and Development. Paris

    2014-01-01

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

  7. Uranium 2005 Resources, Production and Demand

    CERN Document Server

    Organisation for Economic Cooperation and Development. Paris. Nuclear Energy Agency

    2006-01-01

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

  8. A general overview of generation IV molten salt reactor (MSR) and the use of thorium as fuel

    Energy Technology Data Exchange (ETDEWEB)

    Yamaguchi, Carlos H.; Stefani, Giovanni L.; Santos, Thiago A., E-mail: carlos.yamaguchi@usp.br, E-mail: giovanni.stefani@ipen.br, E-mail: thiago.santos@ufabc.edu.br [Universidade de Sao Paulo (USP), SP (Brazil). Instituto de Fisica; Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Universidade Federal do ABC (CECS/UFABC), Santo Andre, SP (Brazil). Centro de Engenharia, Modelagem e Ciencias Sociais Aplicadas

    2017-07-01

    The molten salt reactors (MSRs) make use of fluoride salt as primary cooler, at low pressure. Although considered a generation IV reactor, your concept isn't new, since in the 1960 years the Oak Ridge National Laboratory created a little prototype of 8MWt. Over the 20{sup th} century, other countries, like UK, Japan, Russia, China and France also did research in the area, especially with the use of thorium as fuel. This goes with the fact that Brazil possess the biggest reserve of thorium in the world. In the center of nuclear engineering at IPEN is being created a study group connected to thorium reactors, which purpose is to investigate reactors using thorium to produce {sup 233}U and tailing burn, thus making the MSR using thorium as fuel, an object of study. This present work searches to do a general summary about the researches of MSR's, having as focus the utilization of thorium with the goal being to show it's efficiency and utilization is doable. (author)

  9. Geology of uranium in the Chadron area, Nebraska and South Dakota

    Science.gov (United States)

    Dunham, Robert Jacob

    1961-01-01

    The Chadron area covers 375 square miles about 25 miles southeast of the Black Hills. Recurrent mild tectonic activity and erosion on the Chadron arch, a compound anticlinal uplift of regional extent, exposed 1900 feet of Upper Cretaceous rocks, mostly marine shale containing pyrite and organic matter, and 600 feet of Oligocene and Miocene rocks, mostly terrestrial fine-grained sediment containing volcanic ash. Each Cretaceous formation truncated by the sub-Oligocene unconformity is stained yellow and red, leached, kaolinized, and otherwise altered to depths as great as 55 feet. The composition and profile of the altered material indicate lateritic soil; indirect evidence indicates Eocene(?) age. In a belt through the central part of the area, the Brule formation of Oligocene age is a sequence of bedded gypsum, clay, dolomite, and limestone more than 300 feet thick. Uranium in Cretaceous shale in 58 samples averages 0.002 percent, ten times the average for the earths crust. Association with pyrite and organic matter indicates low valency. The uranium probably is syngenetic or nearly so. Uranium in Eocene(?) soil in 43 samples averages 0.054 percent, ranging up to 1.12 percent. The upper part of the soil is depleted in uranium; enriched masses in the basal part of the soil consist of remnants of bedrock shale and are restricted to the highest reaches of the ancient oxidation-reduction interface. The uranium is probably in the from of a low-valent mineral, perhaps uraninite. Modern weathering of Cretaceous shale is capable of releasing as much as 0.780 ppm uranium to water. Eocene(?) weathering probably caused enrichment of the ancient soil through 1) leaching of Cretaceous shale, 2) downward migration of uranyl complex ions, and 3) reduction of hydrogen sulfide at the water table. Uranium minerals occur in the basal 25 feet of the gypsum facies of the Brule formation at the two localities where the gypsum is carbonaceous; 16 samples average 0.066 percent uranium and

  10. Uranium resources and uranium supply; Uranvorkommen und Uranversorgung

    Energy Technology Data Exchange (ETDEWEB)

    Barthel, F.; Wellmer, F.W. [Bundesanstalt fuer Geowissenschaften und Rohstoffe Hannover, Hannover (Germany)

    2001-10-01

    The availability of natural uranium is currently considered unproblematic. Out of concern about the sufficient availability of uranium, an international working group of OECD-NEA, in which the Federal Office for Geosciences and Resources (BGR) participates as a German partner, has conducted analyses of uranium availability since 1965. Its findings are published biannually in the so-called 'Red Book', 'Uranium, Resources, Production, and Demand'. Changes in the political situation worldwide have profoundly influenced the military importance of uranium and thus also greatly improved its accessibility. As a consequence, there was a decline in production in the nineties from approx. 57,000 t of U in 1989 to, at present (2001), approx. 35,000 t annually. Estimates of the worldwide requirement of natural uranium in 2015 range between approx. 55,000 t and 80,000 t of U, because of the unforeseeable extent of the use of nuclear power, as against approx. 63,000 t of U in 2001. The most recent statistics published in the 1999 Red Bock show low-cost reserves (up to Dollar 40 per kg of U) of 1325 million t, and 2234 t of uranium at extraction costs of up to t Dollar 80 per kg. This indicates a statistical range of reserves of approx. 35 years. It should be noted that these figures are snapshots of a dynamic system. A resumption of extensive exploration and technical developments could greatly influence the resource situation. In the nineties, for instance, there is a net increase in uranium reserves of approx. 700,000 t of U as a consequence of exploration activities. (orig.) [German] Die Verfuegbarkeit von Natururan wird derzeit als unproblematisch angesehen. Aufgrund der Sorge um eine ausreichende Verfuegbarkeit von Uran beschaeftigt sich seit 1965 eine internationale Arbeitsgruppe der OECD-NEA unter deutscher Beteiligung der Bundesanstalt fuer Geowissenschaften und Rohstoffe (BGR) mit Analysen zur Verfuegbarkeit von Uran. Die Ergebnisse werden alle zwei

  11. Ten-dimensional Supergravity Revisited

    NARCIS (Netherlands)

    Bergshoeff, Eric; Roo, Mees de; Kerstan, Sven; Riccioni, Fabio; Diaz Alonso, J.; Mornas, L.

    2006-01-01

    We show that the exisiting supergravity theories in ten dimensions can be extended with extra gauge fields whose rank is equal to the spacetime dimension. These gauge fields have vanishing field strength but nevertheless play an important role in the coupling of supergravity to spacetime filling

  12. Ten Problems in Experimental Mathematics

    Energy Technology Data Exchange (ETDEWEB)

    Bailey, David H.; Borwein, Jonathan M.; Kapoor, Vishaal; Weisstein, Eric

    2004-09-30

    This article was stimulated by the recent SIAM ''100 DigitChallenge'' of Nick Trefethen, beautifully described in a recent book. Indeed, these ten numeric challenge problems are also listed in a recent book by two of present authors, where they are followed by the ten symbolic/numeric challenge problems that are discussed in this article. Our intent was to present ten problems that are characteristic of the sorts of problems that commonly arise in ''experimental mathematics''. The challenge in each case is to obtain a high precision numeric evaluation of the quantity, and then, if possible, to obtain a symbolic answer, ideally one with proof. Our goal in this article is to provide solutions to these ten problems, and in the process present a concise account of how one combines symbolic and numeric computation, which may be termed ''hybrid computation'', in the process of mathematical discovery.

  13. Understanding Scale: Powers of Ten

    Science.gov (United States)

    Jones, M. Gail; Taylor, Amy; Minogue, James; Broadwell, Bethany; Wiebe, Eric; Carter, Glenda

    2007-01-01

    The classic film "Powers of Ten" is often employed to catalyze the building of more accurate conceptions of scale, yet its effectiveness is largely unknown. This study examines the impact of the film on students' concepts of size and scale. Twenty-two middle school students and six science teachers participated. Students completed pre- and…

  14. A Ten-Year Reflection

    Science.gov (United States)

    Phillip, Cyndi

    2016-01-01

    Five initiatives launched during Cyndi Phillip's term as American Association of School Librarians (AASL) President (2006-2007) continue to have an impact on school librarians ten years later. They include the rewriting of AASL's learning standards, introduction of the SKILLS Act, the presentation of the Crystal Apple Award to Scholastic Library…

  15. Ten Rules of Academic Writing

    NARCIS (Netherlands)

    Donovan, S.K.

    2011-01-01

    Creative writers are well served with 'how to' guides, but just how much do they help? And how might they be relevant to academic authors? A recent survey of writing tips by twenty-eight creative authors has been condensed to the ten most relevant to the academic, supported by some comments on

  16. Ten "Discoveries" About Basic Learning

    Science.gov (United States)

    English, Raymond

    1977-01-01

    Ten conclusions about childrens' learning are presented from 15 years of research by the Educational Research Council of America. These include effectiveness of short textbooks, interest in learning technical words, need for social science curriculum to challenge, and detrimental effect of ingrained teacher attitudes to teach social studies by…

  17. Monitoring of thorium incorporation by thoron in breath measurement: technical design of a routine method

    Energy Technology Data Exchange (ETDEWEB)

    Eisenmenger, A.; Riedel, W.; Scheler, R.; Brose, J

    1998-07-01

    A method for measurement of thoron ({sup 220}Rn) in exhaled air is being developed for routine monitoring of inhaled thorium intakes. Decay products of thoron ({sup 216}Po and {sup 212}Pb) are collected electrostatically and their progeny are measured subsequently by alpha spectrometry. With the equipment presently used the influence of parameters such as chamber volume, collection head geometry and position, supplied high voltage, flow rate and subsequent counting time on the collection efficiency have been investigated. The overall efficiency is approximately 8% at the moment. This makes the method capable of detecting thorium in lungs at an amount of 3% of an ALI (Annual Limit on Intake), for example corresponding to 0.9 Bq of {sup 232}Th (class W), as required by the German radiation protection monitoring guidelines. (author)

  18. Thorium nanochemistry: the solution structure of the Th(IV)-hydroxo pentamer

    Energy Technology Data Exchange (ETDEWEB)

    Walther, Clemens; Rothe, Jörg; Schimmelpfennig, Bernd; Fuss, Markus [Karlsruher

    2012-10-10

    Tetravalent thorium exhibits a strong tendency towards hydrolysis and subsequent polymerization. Polymeric species play a crucial role in understanding thorium solution chemistry, since their presence causes apparent solubility several orders of magnitude higher than predicted by thermodynamic data bases. Although electrospray mass spectrometry (ESI MS) identifies Th(IV) dimers and pentamers unequivocally as dominant species close to the solubility limit, the molecular structure of Th5(OH)y polymers was hitherto unknown. In the present study, X-ray absorption fine structure (XAFS) spectroscopy, high energy X-ray scattering (HEXS) measurements, and quantum chemical calculations are combined to solve the pentamer structure. The most favourable structure is represented by two Th(IV) dimers linked by a central Th(IV) cation through hydroxide bridges.

  19. Cytogenetic biomonitoring of inhabitants of a large uranium mineralization area: the municipalities of Monte Alegre, Prainha, and Alenquer, in the State of Pará, Brazil.

    Science.gov (United States)

    Guimarães, Adriana Costa; Antunes, Lusânia Maria Greggi; Ribeiro, Helem Ferreira; dos Santos, Andrea Kelly Ribeiro; Cardoso, Plínio Cerqueira dos Santos; de Lima, Patrícia Lima; Seabra, Aline Damasceno; Pontes, Thaís Brilhante; Pessoa, Claudia; de Moraes, Manoel Odorico; Cavalcanti, Bruno Coelho; Sombra, Carla Maria Lima; Bahia, Marcelo de Oliveira; Burbano, Rommel Rodríguez

    2010-10-01

    Uranium is a natural radioactive metallic element; its effect on the organism is cumulative, and chronic exposure to this element can induce carcinogenesis. Three cities of the Amazon region-Monte Alegre, Prainha, and Alenquer-in North Brazil, are located in one of the largest uranium mineralization areas of the world. Radon is a radioactive gas, part of uranium decay series and readily diffuses through rock. In Monte Alegre, most of the houses are built of rocks removed from the Earth's crust in the forest, where the uranium reserves lie. The objective of the present work is to determine the presence or absence of genotoxicity and risk of carcinogenesis induced by natural exposure to uranium and radon in the populations of these three cities. The frequency of micronuclei (MN) and chromosomal aberrations (CA) showed no statistically significant differences between the control population and the three study populations (P > 0.05). MN was also analyzed using the fluorescence in situ hybridization (FISH) technique, with a centromere-specific probe. No clastogenic and/or aneugenic effects were found in the populations. Using FISH analysis, other carcinogenesis biomarkers were analyzed, but neither the presence of the IGH/BCL2 translocation nor an amplification of the MYC gene and 22q21 region was detected. Clastogenicity and DNA damage were also not found in the populations analyzed using the alkaline comet assay. The mitotic index showed no cytotoxicity in the analyzed individuals' lymphocytes. Once we do not have data concerning radiation doses from other sources, such as cosmic rays, potassium, thorium, or anthropogenic sources, it is hard to determine if uranium emissions in this geographic region where our study population lives are too low to cause significant DNA damage. Regardless, genetic analyses suggest that the radiation in our study area is not high enough to induce DNA alterations or to interfere with mitotic apparatus formation. It is also possible that

  20. Uranium, plutonium and co

    Energy Technology Data Exchange (ETDEWEB)

    Sauerbrey, Roland; Joehnk, Peter (eds.)

    2016-04-15

    To date there is no repository facility for highly radioactive and heat-generating waste in Germany. This politically ''hot'' topic is undeniably a very big, urgent problem in our society. The Helmholtz Association of German Research Centers is dedicated to developing scientific solutions for such issues. It looks back on 20 years of history: In 1995 the loosely organized collective bearing the name ''Working Association of Large-Scale Research Institutes'' (Arbeitsgemeinschaft der Grossforschungseinrichtungen) became an association of now 18 research centers. These centers collectively work in a total of six research areas. While the HZDR has only belonged to the largest research association in Germany since 2011, repository research was already on the agenda way back when the Rossendorf research center established itself in 1992 after the fall of the Berlin Wall. A good enough reason to examine the results from about 20 years of repository research in Dresden in more detail. In this issue of ''discovered'' we will take an inside look at radiochemical, radiogeological, and microbiological labs, look over the shoulders of researchers using the ''Rossendorf Beamline'' at the European Synchrotron Radiation Facility in Grenoble, and descend hundreds of meters into Finnish, Swedish, and Swiss research labs. How do ''uranium, plutonium, and co.'' react with mineral surfaces in environments that are low in oxygen or watery? How do they interact with microorganisms deep underground? And how can host rock or other materials be used as technical barriers to prevent the spread of radioactive substances? In order to answer these and further questions, the researchers of the HZDR use a wide range of spectroscopic methods. They expose test samples to lasers, infrared light, and X-rays or use the fluorescent properties of certain compounds to learn about the behavior of actinides

  1. Ten past and ten future GAS/MAUS-payloads

    Science.gov (United States)

    Staniek, S.; Otto, G.; Doepkess, J.

    1988-01-01

    MAUS (materials science autonomous experiments) is one out of a series of flight opportunities which the Space Program of West Germany offers to scientists from the disciplines of materials research and processing for performing materials science investigations under microgravity conditions. Up to now, ten MAUS experiments were flown which were dealing with the following scientific topics: decomposition of binary alloys with miscibility gap in the liquid state, interaction of a solidification front with dispersed particles, critical Marangoni number, investigation of the magnetic compound MnBi, shrinkage of gas bubbles in glass melts and slip casting. The ten future experiments are partly reflights with modification of the scientific objectives as well as new experiments in the fields of chemical reactions, heat transfer, glass technology and Ostwald ripening. Looking to ten flown payloads, the peculiarities of instrument technology in GAS-cans and its evolution is discussed with emphasis on structure, electronics and thermal design. A typical modern payload using 100 percent of the resource is presented.

  2. A study of thorium exposure during tungsten inert gas welding in an airline engineering population.

    Science.gov (United States)

    McElearney, N; Irvine, D

    1993-07-01

    To investigate the theoretic possibility of excessive exposure to thorium during the process of tungsten inert gas (TIG) welding using thoriated rods we carried out a cross-sectional study of TIG welders and an age- and skill-matched group. We measured the radiation doses from inhaled thorium that was retained in the body and investigated whether any differences in health or biologic indices could have been attributable to the welding and tip-grinding process. Sixty-four TIG welders, 11 non-TIG welders, and 61 control subjects from an airline engineering population participated. All of the subjects were interviewed for biographic, occupational history and morbidity details. All of the welders and eight control subjects carried out large-volume urine sampling to recover thorium 232 and thorium 228; this group also had chest radiographs. All of the subjects had a blood sample taken to estimate liver enzymes, and they provided small-volume urine samples for the estimation of retinol-binding protein and beta 2-microglobulin. We found no excess of morbidity among the TIG or non-TIG welding groups, and the levels of retinol-binding protein and beta 2-microglobulin were the same for both groups. There was a higher aspartate aminotransferase level in the control group. The internal radiation doses were estimated at less than an annual level of intake in all cases, and considerably less if the exposure (as was the case) was assumed to be chronic over many years. Some additional precautionary measures are suggested to reduce further any potential hazard from this process.

  3. Cycle for fuel elements. Uranium production, programs for nuclear power stations and capital expenditure involved; Cycles de combustibles. Production d'uranium, programme de centrales electriques et effort financier correspondant

    Energy Technology Data Exchange (ETDEWEB)

    Andriot, J.; Gaussens, J. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1958-07-01

    A number of different possible programs for nuclear power stations of various types are presented in this survey. These programs are established in relation to the use of uranium and thorium in amounts similar to those that shall probably be produced in France during the next fifteen years. As it is possible to draw plans for nuclear power stations in which several processes exist simultaneously, an unlimited number of variations being thinkable, this survey is limited to successive analysis of the results obtained by use of only one of each of the following three systems: - system natural uranium-graphite, - system natural uranium-heavy water, -system enriched uranium-pressurised light water. All schemes are considered as assemblages of these three simple systems. The effects of plutonium recycling are also considered for each system. The electric power installed and the capacity of stations situated up-stream and down-stream have been calculated by this method and an attempt has been made to establish the sum to be invested during the fifteen years necessary for the launching of the programs scheduled. A table of timing for the investments groups the results obtained. Considering the fact that French availabilities in capital shall not be unlimited during the coming years, this way of presenting the results seems to be interesting. (author)Fren. [French] L'etude presentee comporte l'examen d'un certain nombre d'hypotheses de programmes de centrales nucleaires de types differents. Ces programmes correspondent a l'utilisation de tonnages d'uranium et de thorium de l'ordre de grandeur de ceux qui seront probablement produits par la France dans les quinze prochaines annees. Comme il est possible de batir un programme de centrales nucleaires, comportant a la fois plusieurs filieres suivant des variantes en nombre infini, on s'est contente d'examiner successivement les resultats ous si on utilisait exclusivement l

  4. Inherently safe in situ uranium recovery.

    Energy Technology Data Exchange (ETDEWEB)

    Krumhansl, James Lee; Beauheim, Richard Louis; Brady, Patrick Vane; Arnold, Bill Walter; Kanney, Joseph F.; McKenna, Sean Andrew

    2009-05-01

    Expansion of uranium mining in the United States is a concern to some environmental groups and sovereign Native American Nations. An approach which may alleviate some problems is to develop inherently safe in situ uranium recovery ('ISR') technologies. Current ISR technology relies on chemical extraction of trace levels of uranium from aquifers that, once mined, can still contain dissolved uranium and other trace metals that are a health concern. Existing ISR operations are few in number; however, high uranium prices are driving the industry to consider expanding operations nation-wide. Environmental concerns and enforcement of the new 30 ppb uranium drinking water standard may make opening new mining operations more difficult and costly. Here we propose a technological fix: the development of inherently safe in situ recovery (ISISR) methods. The four central features of an ISISR approach are: (1) New 'green' leachants that break down predictably in the subsurface, leaving uranium, and associated trace metals, in an immobile form; (2) Post-leachant uranium/metals-immobilizing washes that provide a backup decontamination process; (3) An optimized well-field design that increases uranium recovery efficiency and minimizes excursions of contaminated water; and (4) A combined hydrologic/geochemical protocol for designing low-cost post-extraction long-term monitoring. ISISR would bring larger amounts of uranium to the surface, leave fewer toxic metals in the aquifer, and cost less to monitor safely - thus providing a 'win-win-win' solution to all stakeholders.

  5. Poisson regression analysis of mortality among male workers at a thorium-processing plant

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Zhiyuan; Lee, Tze-San; Kotek, T.J.

    1991-12-31

    Analyses of mortality among a cohort of 3119 male workers employed between 1915 and 1973 at a thorium-processing plant were updated to the end of 1982. Of the whole group, 761 men were deceased and 2161 men were still alive, while 197 men were lost to follow-up. A total of 250 deaths was added to the 511 deaths observed in the previous study. The standardized mortality ratio (SMR) for all causes of death was 1.12 with 95% confidence interval (CI) of 1.05-1.21. The SMRs were also significantly increased for all malignant neoplasms (SMR = 1.23, 95% CI = 1.04-1.43) and lung cancer (SMR = 1.36, 95% CI = 1.02-1.78). Poisson regression analysis was employed to evaluate the joint effects of job classification, duration of employment, time since first employment, age and year at first employment on mortality of all malignant neoplasms and lung cancer. A comparison of internal and external analyses with the Poisson regression model was also conducted and showed no obvious difference in fitting the data on lung cancer mortality of the thorium workers. The results of the multivariate analysis showed that there was no significant effect of all the study factors on mortality due to all malignant neoplasms and lung cancer. Therefore, further study is needed for the former thorium workers.

  6. Gas-Cooled Thorium Reactor with Fuel Block of the Unified Design

    Directory of Open Access Journals (Sweden)

    Igor Shamanin

    2015-01-01

    Full Text Available Scientific researches of new technological platform realization carried out in Russia are based on ideas of nuclear fuel breeding in closed fuel cycle and physical principles of fast neutron reactors. Innovative projects of low-power reactor systems correspond to the new technological platform. High-temperature gas-cooled thorium reactors with good transportability properties, small installation time, and operation without overloading for a long time are considered perspective. Such small modular reactor systems at good commercial, competitive level are capable of creating the basis of the regional power industry of the Russian Federation. The analysis of information about application of thorium as fuel in reactor systems and its perspective use is presented in the work. The results of the first stage of neutron-physical researches of a 3D model of the high-temperature gas-cooled thorium reactor based on the fuel block of the unified design are given. The calculation 3D model for the program code of MCU-5 series was developed. According to the comparison results of neutron-physical characteristics, several optimum reactor core compositions were chosen. The results of calculations of the reactivity margins, neutron flux distribution, and power density in the reactor core for the chosen core compositions are presented in the work.

  7. Separation of thorium (IV) from lanthanide concentrate (LC) and water leach purification (WLP) residue

    Energy Technology Data Exchange (ETDEWEB)

    AL-Areqi, Wadeeah M.; Majid, Amran Ab.; Sarmani, Sukiman [Nuclear Science Programme, School of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor (Malaysia)

    2014-09-03

    Thorium (IV) content in industrial residue produced from rare earth elements production industry is one of the challenges to Malaysian environment. Separation of thorium from the lanthanide concentrate (LC) and Water Leach Purification (WLP) residue from rare earth elements production plant is described. Both materials have been tested by sulphuric acid and alkaline digestions. Th concentrations in LC and WLP were determined to be 1289.7 ± 129 and 1952.9±17.6 ppm respectively. The results of separation show that the recovery of Th separation from rare earth in LC after concentrated sulphuric acid dissolution and reduction of acidity to precipitate Th was found 1.76-1.20% whereas Th recovery from WLP was less than 4% after concentrated acids and alkali digestion processes. Inductively Coupled Plasma-Mass Spectroscopy (ICP-MS) was used to determine Th concentrations in aqueous phase during separation stages. This study indicated that thorium maybe exists in refractory and insoluble form which is difficult to separate by these processes and stays in WLP residue as naturally occurring radioactive material (NORM)

  8. Depleted uranium: Metabolic disruptor?; Uranium appauvri: perturbateur metabolique?

    Energy Technology Data Exchange (ETDEWEB)

    Souidi, Maamar; Dublineau, Isabelle; Lestaevel, Philippe [Institut de Radioprotection et de Surete Nucleaire - IRSN, Direction de la radioprotection de l' homme, Laboratoire de radiotoxicologie experimentale, Service de radiobiologie et d' epidemiologie, BP 17, 92262 Fontenay-aux-Roses cedex (France)

    2011-11-15

    The presence of uranium in the environment can lead to long-term contamination of the food chain and of water intended for human consumption and thus raises many questions about the scientific and societal consequences of this exposure on population health. Although the biological effects of chronic low-level exposure are poorly understood, results of various recent studies show that contamination by depleted uranium (DU) induces subtle but significant biological effects at the molecular level in organs including the brain, liver, kidneys and testicles. For the first time, it has been demonstrated that DU induces effects on several metabolic pathways, including those metabolizing vitamin D, cholesterol, steroid hormones, acetylcholine and xenobiotics. This evidence strongly suggests that DU might well interfere with many metabolic pathways. It might thus contribute, together with other man-made substances in the environment, to increased health risks in some regions. (authors)

  9. Reports on investigations of uranium anomalies. National Uranium Resource Evaluation

    Energy Technology Data Exchange (ETDEWEB)

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

    1982-10-01

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

  10. Three-dimensional MOF-type architectures with tetravalent uranium hexanuclear motifs (U{sub 6}O{sub 8})

    Energy Technology Data Exchange (ETDEWEB)

    Falaise, Clement; Volkringer, Christophe; Vigier, Jean-Francois; Henry, Natacha; Beaurain, Arnaud; Loiseau, Thierry [Unite de Catalyse et Chimie du Solide (UCCS), UMR CNRS 8181, Universite de Lille Nord de France, USTL-ENSCL, Villeneuve d' Ascq (France)

    2013-04-22

    Four metal-organic frameworks (MOF) with tetravalent uranium have been solvothermally synthesized by treating UCl{sub 4} with rigid dicarboxylate linkers in N,N-dimethylfomamide (DMF). The use of the ditopic ligands 4,4{sup '}-biphenyldicarboxylate (1), 2,6-naphthalenedicarboxylate (2), terephthalate (3), and fumarate (4) resulted in the formation of three-dimensional networks based on the hexanuclear uranium-centered motif [U{sub 6}O{sub 4}(OH){sub 4}(H{sub 2}O){sub 6}]. This motif corresponds to an octahedral configuration of uranium nodes and is also known for thorium in crystalline solids. The atomic arrangement of this specific building unit with organic linkers is similar to that found in the zirconium-based porous compounds of the UiO-66/67 series. The structure of [U{sub 6}O{sub 4}(OH){sub 4}(H{sub 2}O){sub 6}(L){sub 6}].X (L=dicarboxylate ligand; X=DMF) shows the inorganic hexamers connected in a face-centered cubic manner through the ditopic linkers to build up a three-dimensional framework that delimits octahedral (from 5.4 Aa for 4 up to 14.0 Aa for 1) and tetrahedral cavities. The four compounds have been characterized by using single-crystal X-ray diffraction analysis (or powder diffraction analysis for 4). The tetravalent state of uranium has been examined by using XPS and solid-state UV/Vis analyses. The measurement of the Brunauer-Emmett-Teller surface area indicated very low values (Langmuir <300 m{sup 2} g{sup -1} for 1, <7 m{sup 2} g{sup -1} for 2-4) and showed that the structures are quite unstable upon removal of the encapsulated DMF solvent. (Copyright copyright 2013 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  11. Health Impact of Uranium in Phosphate Fertilizers - Assessing the radiological impact of using Israeli phosphate fertilizers: A critical review

    Energy Technology Data Exchange (ETDEWEB)

    Moinester, Murray [Tel Aviv University, School of Physics and Astronomy, 69978 Tel Aviv (Israel); Kronfeld, Joel [Tel Aviv University, Department of Geosciences, 69978 Tel Aviv (Israel)

    2014-07-01

    Of the three main ingredients used in agricultural nitrogen, phosphorous, and potassium (NPK) fertilizers in Israel and elsewhere, two of them, the phosphorous and potassium additions, contain radio-elements. The P is derived from the use of Senonian aged phosphorite. The extensive Israeli phosphorite deposits (averaging approximately 140 ppm uranium) can be considered a potential low grade uranium ore. Sufficient time has passed since the deposits were laid down for secular equilibrium to be achieved in the uranium decay-series. Thus, deposits now include radioactive daughters thorium, radium, radon, polonium and lead. Besides being radioactive, these or their daughters are biologically deleterious elements. The potential dangers of using enriched phosphate derivatives are both that of adding phosphate radio-metals to the agricultural soils, the uptake by crops, their leakage to the underlying aquifers; or contrariwise, their retention and long term residence in the agricultural top soils. The latter needs to be considered over time, as farmlands are increasingly converted to urban housing. Based upon open sourced literature from Israel and other countries where phosphate fertilizers have been employed, the implications of the above potential problems are reviewed and evaluated. It appears at the moment, that for Israel, the use of phosphate fertilization does not present an immediate health hazard by increasing external dose rates or via crop uptake. However, a continuing build-up of radio-metals over the phreatic aquifers may at some point of time in the future warrant a more rigorous monitoring of the water supplies. Various methods of cleaning soils of the radio-metal contamination are available, though cost via conventional methods would be prohibitive. Though, some of the radionuclides congregate in the phosphogypsum phase during the industrial process, it is currently feasible, if not entirely economical at current depressed prices, to efficiently extract

  12. [Depleted uranium: radiation and ecological safety aspects].

    Science.gov (United States)

    Ushakov, I B; Afanas'ev, R V; Berezin, G I; Zuev, V G

    2003-01-01

    The authors have analyzed the ecological, sanitary-and-hygienic and medicobiologic aspects of using the impoverished uranium in armaments and military equipment. The influence of impoverished uranium on human body (600 cases) was studied using medicobiologic investigation. It was shown that the particles of aerosol of mixed uranium oxide cause the radiation and chemical damage of kidneys, lungs and other internals. Uranium's alpha-radiation is very effective in induction of biologic effects during internal irradiation. Taking into account that bone tissue is the critical organ for uranium isotopes the medullar tissue is exposed to alpha-radiation. In the armed conflicts of the last decade wide use of armour-piercing means with elements consisted of impoverished uranium has led to the appearance of new technogenic risk factor for the environment and the man.

  13. Deposit model for volcanogenic uranium deposits

    Science.gov (United States)

    Breit, George N.; Hall, Susan M.

    2011-01-01

    Volcanism is a major contributor to the formation of important uranium deposits both close to centers of eruption and more distal as a result of deposition of ash with leachable uranium. Hydrothermal fluids that are driven by magmatic heat proximal to some volcanic centers directly form some deposits. These fluids leach uranium from U-bearing silicic volcanic rocks and concentrate it at sites of deposition within veins, stockworks, breccias, volcaniclastic rocks, and lacustrine caldera sediments. The volcanogenic uranium deposit model presented here summarizes attributes of those deposits and follows the focus of the International Atomic Energy Agency caldera-hosted uranium deposit model. Although inferred by some to have a volcanic component to their origin, iron oxide-copper-gold deposits with economically recoverable uranium contents are not considered in this model.

  14. Uranium 2009 resources, production and demand

    CERN Document Server

    Organisation for Economic Cooperation and Development. Paris

    2010-01-01

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

  15. Maximum permissible concentrations of uranium in air

    CERN Document Server

    Adams, N

    1973-01-01

    The retention of uranium by bone and kidney has been re-evaluated taking account of recently published data for a man who had been occupationally exposed to natural uranium aerosols and for adults who had ingested uranium at the normal dietary levels. For life-time occupational exposure to uranium aerosols the new retention functions yield a greater retention in bone and a smaller retention in kidney than the earlier ones, which were based on acute intakes of uranium by terminal patients. Hence bone replaces kidney as the critical organ. The (MPC) sub a for uranium 238 on radiological considerations using the current (1959) ICRP lung model for the new retention functions is slightly smaller than for earlier functions but the (MPC) sub a determined by chemical toxicity remains the most restrictive.

  16. Biological processes for concentrating trace elements from uranium mine waters. Technical completion report

    Energy Technology Data Exchange (ETDEWEB)

    Brierley, C.L.; Brierley, J.A.

    1981-12-01

    Waste water from uranium mines in the Ambrosia Lake district near Grants, New Mexico, USA, contains uranium, selenium, radium and molybdenum. The Kerr-McGee Corporation has a novel treatment process for waters from two mines to reduce the concentrations of the trace contaminants. Particulates are settled by ponding, and the waters are passed through an ion exchange resin to remove uranium; barium chloride is added to precipitate sulfate and radium from the mine waters. The mine waters are subsequently passed through three consecutive algae ponds prior to discharge. Water, sediment and biological samples were collected over a 4-year period and analyzed to assess the role of biological agents in removal of inorganic trace contaminants from the mine waters. Some of the conclusions derived from this study are: (1) The concentrations of soluble uranium, selenium and molybdenum were not diminished in the mine waters by passage through the series of impoundments which constituted the mine water treatment facility. Uranium concentrations were reduced but this was due to passage of the water through an ion exchange column. (2) The particulate concentrations of the mine water were reduced at least ten-fold by passage of the waters through the impoundments. (3) The sediments were anoxic and enriched in uranium, molybdenum and selenium. The deposition of particulates and the formation of insoluble compounds were proposed as mechanisms for sediment enrichment. (4) The predominant algae of the treatment ponds were the filamentous Spirogyra and Oscillatoria, and the benthic alga, Chara. (5) Adsorptive processes resulted in the accumulation of metals in the algae cells. (6) Stimulation of sulfate reduction by the bacteria resulted in retention of molybdenum, selenium, and uranium in sediments. 1 figure, 16 tables.

  17. METHOD OF PRODUCING URANIUM METAL BY ELECTROLYSIS

    Science.gov (United States)

    Piper, R.D.

    1962-09-01

    A process is given for making uranium metal from oxidic material by electrolytic deposition on the cathode. The oxidic material admixed with two moles of carbon per one mole of uranium dioxide forms the anode, and the electrolyte is a mixture of from 40 to 75% of calcium fluoride or barium fluoride, 15 to 45% of uranium tetrafluoride, and from 10 to 20% of lithium fluoride or magnesium fluoride; the temperature of the electrolyte is between 1150 and 1175 deg C. (AEC)

  18. Distribution of uranium-bearing phases in soils from Fernald

    Energy Technology Data Exchange (ETDEWEB)

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

    1993-12-31

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

  19. Oxidation and crystal field effects in uranium

    Energy Technology Data Exchange (ETDEWEB)

    Tobin, J. G. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Booth, C. H. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Shuh, D. K. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); van der Laan, G. [Diamond Light Source, Didcot (United Kingdom); Sokaras, D. [Stanford Synchrotron Radiation Lightsource, Stanford, CA (United States); Weng, T. -C. [Stanford Synchrotron Radiation Lightsource, Stanford, CA (United States); Yu, S. W. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Bagus, P. S. [Univ. of North Texas, Denton, TX (United States); Tyliszczak, T. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Nordlund, D. [Stanford Synchrotron Radiation Lightsource, Stanford, CA (United States)

    2015-07-06

    An extensive investigation of oxidation in uranium has been pursued. This includes the utilization of soft x-ray absorption spectroscopy, hard x-ray absorption near-edge structure, resonant (hard) x-ray emission spectroscopy, cluster calculations, and a branching ratio analysis founded on atomic theory. The samples utilized were uranium dioxide (UO2), uranium trioxide (UO3), and uranium tetrafluoride (UF4). As a result, a discussion of the role of non-spherical perturbations, i.e., crystal or ligand field effects, will be presented.

  20. Ten questions about systems biology

    DEFF Research Database (Denmark)

    Joyner, Michael J; Pedersen, Bente K

    2011-01-01

    In this paper we raise 'ten questions' broadly related to 'omics', the term systems biology, and why the new biology has failed to deliver major therapeutic advances for many common diseases, especially diabetes and cardiovascular disease. We argue that a fundamentally narrow and reductionist...... to understand how whole animals adapt to the real world. We argue that a lack of fluency in these concepts is a major stumbling block for what has been narrowly defined as 'systems biology' by some of its leading advocates. We also point out that it is a failure of regulation at multiple levels that causes many...

  1. Ten questions about systems biology

    DEFF Research Database (Denmark)

    Joyner, Michael J; Pedersen, Bente K

    2011-01-01

    to understand how whole animals adapt to the real world. We argue that a lack of fluency in these concepts is a major stumbling block for what has been narrowly defined as 'systems biology' by some of its leading advocates. We also point out that it is a failure of regulation at multiple levels that causes many......In this paper we raise 'ten questions' broadly related to 'omics', the term systems biology, and why the new biology has failed to deliver major therapeutic advances for many common diseases, especially diabetes and cardiovascular disease. We argue that a fundamentally narrow and reductionist...

  2. Ten Blue Links on Mars

    OpenAIRE

    Clarke, Charles L. A.; Cormack, Gordon V.; Lin, Jimmy; Roegiest, Adam

    2016-01-01

    This paper explores a simple question: How would we provide a high-quality search experience on Mars, where the fundamental physical limit is speed-of-light propagation delays on the order of tens of minutes? On Earth, users are accustomed to nearly instantaneous response times from search engines. Is it possible to overcome orders-of-magnitude longer latency to provide a tolerable user experience on Mars? In this paper, we formulate the searching from Mars problem as a tradeoff between "effo...

  3. Ten Thousand Years of Solitude

    Energy Technology Data Exchange (ETDEWEB)

    Benford, G. (Los Alamos National Lab., NM (USA) California Univ., Irvine, CA (USA). Dept. of Physics); Kirkwood, C.W. (Los Alamos National Lab., NM (USA) Arizona State Univ., Tempe, AZ (USA). Coll. of Business Administration); Harry, O. (Los Alamos National Lab., NM (USA)); Pasqualetti, M.J. (Los Alamos National Lab., NM (USA) Arizona State Univ., Tempe, AZ (USA))

    1991-03-01

    This report documents the authors work as an expert team advising the US Department of Energy on modes of inadvertent intrusion over the next 10,000 years into the Waste Isolation Pilot Project (WIPP) nuclear waste repository. Credible types of potential future accidental intrusion into the WIPP are estimated as a basis for creating warning markers to prevent inadvertent intrusion. A six-step process is used to structure possible scenarios for such intrusion, and it is concluded that the probability of inadvertent intrusion into the WIPP repository over the next ten thousand years lies between one and twenty-five percent. 3 figs., 5 tabs.

  4. Radiotracer study of thorium complexation with humic acid at pH 2-11 using free-liquid electrophoresis

    Energy Technology Data Exchange (ETDEWEB)

    Benes, P. [Czech Technical Univ., Prague (Czech Republic). Dept. of Nuclear Chemistry

    2009-07-01

    Free-liquid electrophoresis was used for the study of thorium complexation with Aldrich humic acid (HA) in aqueous solutions of 0.01 M (NaClO{sub 4} + HClO{sub 4} or NaOH) with dependence on pH and concentration of thorium ({<=} 10{sup -9} - 10{sup -5} M, labelled with {sup 234}Th) and HA (0.1-10 mg/L). The abundances and the mean electrophoretic mobilities of thorium humate complexes were calculated from the electrophoretic mobilities of thorium measured. It has been found that negatively charged humate complexes dominate in the solutions of pH 2-11 containing 1-10 mg/L HA and up to 0.001 M HCO{sub 3}{sup -}. Experimental evidence was given of the formation of Th(OH){sub 4}HA{sup y-} complex at pH 8-11 and its stability constant was determined. New conclusions about spontaneous association of HA molecules at pH 2-6 and about binding of thorium by non-dissociated carboxyl groups of HA were drawn. (orig.)

  5. Geological and geochronological evidence for the effect of Paleogene and Miocene uplift of the Northern Ordos Basin on the formation of the Dongsheng uranium district, China

    Science.gov (United States)

    Zhang, Chuang; Yi, Chao; Dong, Qian; Cai, Yu-Qi; Liu, Hong-Xu

    2018-02-01

    The Dongsheng uranium district, located in the northern part of the Ordos Basin, contains the largest known sandstone-hosted uranium deposit in China. This district contains (from west to east) the Daying, Nalinggou, and Dongsheng uranium deposits that host tens of thousands of metric tonnes of estimated recoverable uranium resources at an average grade of 0.05% U. These uranium orebodies are generally hosted by the lower member of the Zhiluo Formation and are dominantly roll or tabular in shape. The uranium deposits in this district formed during two stages of mineralization (as evidenced by U-Pb dating) that occurred at 65-60 and 25 Ma. Both stages generated coffinite, pitchblende, anatase, pyrite, and quartz, with or without sericite, chlorite, calcite, fluorite, and hematite. The post-Late Cretaceous uplift of the Northern Ordos Basin exposed the northern margins of the Zhiluo Formation within the Hetao depression at 65-60 Ma, introducing groundwater into the formation and generating the first stage of uranium mineralization. The Oligocene (∼25 Ma) uplift of this northern margin exposed either the entirety of the southern flank of the Hetao depression or only the clastic sedimentary part of this region, causing a second gravitational influx of groundwater into the Zhiluo Formation and forming the second stage of uranium mineralization.

  6. Electroreduction of uranium(VI) to uranium(IV) in strip product solutions

    Science.gov (United States)

    Skripchenko, S. Yu.; Chernyshov, M. V.; Smirnov, A. L.

    2017-09-01

    The electrochemical reduction of uranium(VI) to uranium(IV) in strip product solutions on a carbon electrode was investigated. The maximal tetravalent uranium yield as well as a high current efficiency could be achieved during the electrolysis at current densities of 8-10 mA/cm2. The use of solutions with fluoride ions addition for electrolysis resulted in increased process efficiency due to formation of fluoride complexes. The efficiency of the electrochemical reduction also increased with increasing uranium content in the strip product solutions. The addition of hydrazine in solution was very effective for preventing nitric acid reduction at cathode, oxidation of uranium ions and anode destruction.

  7. Cracked lifting lug welds on ten-ton UF{sub 6} cylinders

    Energy Technology Data Exchange (ETDEWEB)

    Dorning, R.E. [Martin Marietta Energy Systems, Inc., Piketon, OH (United States)

    1991-12-31

    Ten-ton, Type 48X, UF{sub 6} cylinders are used at the Portsmouth Gaseous Diffusion Plant to withdraw enriched uranium hexafluoride from the cascade, transfer enriched uranium hexafluoride to customer cylinders, and feed enriched product to the cascade. To accomplish these activities, the cylinders are lifted by cranes and straddle carriers which engage the cylinder lifting lugs. In August of 1988, weld cracks on two lifting lugs were discovered during preparation to lift a cylinder. The cylinder was rejected and tagged out, and an investigating committee formed to determine the cause of cracking and recommend remedial actions. Further investigation revealed the problem may be general to this class of cylinder in this use cycle. This paper discusses the actions taken at the Portsmouth site to deal with the cracked lifting lug weld problem. The actions include inspection activities, interim corrective actions, metallurgical evaluation of cracked welds, weld repairs, and current monitoring/inspection program.

  8. The Spectral Shift Control Reactor as an option for much improved uranium utilisation in single-batch SMRs

    Energy Technology Data Exchange (ETDEWEB)

    Lindley, B.A., E-mail: bal29@cam.ac.uk; Parks, G.T.

    2016-12-01

    Highlights: • A PWR with mixed D{sub 2}O/H{sub 2}O moderator/coolant is investigated for SMR applications. • Heavy water concentration varied over the cycle to give ‘spectral shift’ operation. • Much wetter lattice than normal is neutronically favourable. • Taller fuel stack is thus needed to ensure acceptable MDNBR. • 35–43% increase in uranium utilisation for single batch reactor is possible. - Abstract: The Spectral Shift Control Reactor (SSCR) uses a mix of D{sub 2}O and H{sub 2}O to moderate and cool the reactor. Initially, a high proportion of D{sub 2}O is used, such that the reactor is substantially under-moderated, with excess neutrons being primarily captured in {sup 238}U, breeding {sup 239}Pu. Towards the end of the cycle (EOC), the coolant is predominantly H{sub 2}O, thermalising the neutron spectrum and increasing reactivity. Recently, small modular reactors (SMRs) have gained significant interest as a means of providing a power source that requires little maintenance and refuelling. This motivates long cycles and reduced batch operation. For a single-batch reactor, there is typically a 33% penalty to uranium utilisation compared to a 3-batch reactor. Lattice calculations demonstrate the potential of the SSCR to greatly improve uranium utilisation in single-batch reactors over a range of enrichments. A relatively ‘wet’ lattice is employed which further improves uranium utilisation. Cases with 5% and 15% fissile loading are considered, for which it is respectively possible to achieve 47% and 39% increases in natural uranium utilisation using the SSCR relative to a ‘reference’ light water reactor. In the latter case, if 25% thorium is mixed into the fuel, the improvement in uranium utilisation increases to a total of 49%. Hence, in both cases, it is possible to in effect eliminate the penalty of using a single fuel batch. The ‘wet’ lattice introduces substantial thermal-hydraulic challenges due to the significantly higher fuel

  9. Formation cross-sections and chromatographic separation of protactinium isotopes formed in proton-irradiated thorium metal

    Energy Technology Data Exchange (ETDEWEB)

    Radchenko, Valery; Engle, Jonathan W.; Wilson, Justin J.; Maassen, Joel R.; Nortier, Meiring F.; Birnbaum, Eva R.; John, Kevin D.; Fassbender, Michael E. [Los Alamos National Laboratory, NM (United States)

    2016-08-01

    Targeted alpha therapy (TAT) is a treatment method of increasing interest to the clinical oncology community that utilizes α-emitting radionuclides conjugated to biomolecules for the selective killing of tumor cells. Proton irradiation of thorium generates a number of α-emitting radionuclides with therapeutic potential for application via TAT. In particular, the radionuclide {sup 230}Pa is formed via the {sup 232}Th(p, 3n) nuclear reaction and partially decays to {sup 230}U, an α emitter which has recently received attention as a possible therapy nuclide. In this study, we estimate production yields for {sup 230}Pa and other Pa isotopes from proton-irradiated thorium based on cross section measurements. We adopt existing methods for the chromatographic separation of protactinium isotopes from proton irradiated thorium matrices to combine and optimize them for effective fission product decontamination.

  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

  11. Compilation of criticality data involving thorium or 233U and light water moderation

    Energy Technology Data Exchange (ETDEWEB)

    Gore, B.F.

    1978-07-01

    The literature has been searched for criticality data for light water moderated systems which contain thorium or /sup 233/U, and data found are compiled herein. They are from critical experiments, extrapolations, and exponential experiments performed with homogeneous solutions and metal spheres of /sup 233/U; with lattices of fuel rods containing highly enriched /sup 235/UO/sub 2/ - ThO/sub 2/ and /sup 233/UO/sub 2/ - ThO/sub 2/; and with arrays of cyclinders of /sup 233/U solutions. The extent of existing criticality data has been compared with that necessary to implement a thorium-based fuel cycle. No experiments have been performed with any solutions containing thorium. Neither do data exist for homogeneous /sup 233/U systems with H/U < 34, except for solid metal systems. Arrays of solution cylinders up to 3 x 3 x 3 have been studied. Data for solutions containing fixed or soluble poisons are very limited. All critical lattices using /sup 233/UO/sub 2/ - ThO/sub 2/ fuels (LWBR program) were zoned radially, and in most cases axially also. Only lattice experiments using /sup 235/UO/sub 2/ - ThO/sub 2/ fuels have been performed using a single fuel rod type. Critical lattices of /sup 235/UO/sub 2/ - ThO/sub 2/ rods poisoned with boron have been measured, but only exponential experiments have been performed using boron-poisoned lattices of /sup 233/UO/sub 2/ - ThO/sub 2/ rods. No criticality data exist for denatured fuels (containing significant amounts of /sup 238/U) in either solution or lattice configurations.

  12. 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.

  13. Computer-assisted evaluation of the thermochemical data of the compounds of thorium

    Energy Technology Data Exchange (ETDEWEB)

    Wagman, D. D.; Schumm, R. H.; Parker, V. B.

    1977-08-01

    Selected values are given for the thermochemical properties of the compounds of thorium. They are obtained from a computer-assisted least sums-least squares approach to the evaluation of thermodynamic data networks. The properties given, where data are available, are enthalpy of formation, Gibbs energy of formation, and entropy at 298.15 K (..delta.. Hf (298), ..delta.. Gf (298), and S (298)). The values are consistent with the CODATA Key Values for Thermodynamics. The reaction catalog from which this self consistent set of values is generated is given with a statistical analysis. Some thermal functions are also given, as well as detailed comments when necessary.

  14. Thorium utilization program quarterly progress report for the period ending February 29, 1976. [HTGR Fuel Recycle

    Energy Technology Data Exchange (ETDEWEB)

    1976-03-31

    This publication presents results of work performed under the National HTGR Fuel Recycle Program Thorium Utilization Program. The work reported includes the development of unit processes and equipment for reprocessing of HTGR fuel and the design and development of an integrated line to demonstrate the head end of HTGR reprocessing using unirradiated fuel materials. Work is also described on the development of the conceptual design of recycle facilities to identify the requirements of large-scale recycle of HTGR fuels and to incorporate the results of these studies in guidance of development activities for HTGR fuel recycle.

  15. Study of Chemical Changes in Uranium Oxyfluoride Particles Progress Report March - October 2009

    Energy Technology Data Exchange (ETDEWEB)

    Kips, R; Kristo, M; Hutcheon, I

    2009-11-22

    Nuclear forensics relies on the analysis of certain sample characteristics to determine the origin and history of a nuclear material. In the specific case of uranium enrichment facilities, it is the release of trace amounts of uranium hexafluoride (UF{sub 6}) gas - used for the enrichment of uranium - that leaves a process-characteristic fingerprint. When UF{sub 6} gas interacts with atmospheric moisture, uranium oxyfluoride particles or particle agglomerates are formed with sizes ranging from several microns down to a few tens of nanometers. These particles are routinely collected by safeguards organizations, such as the International Atomic Energy Agency (IAEA), allowing them to verify whether a facility is compliant with its declarations. Spectrometric analysis of uranium particles from UF{sub 6} hydrolysis has revealed the presence of both particles that contain fluorine, and particles that do not. It is therefore assumed that uranium oxyfluoride is unstable, and decomposes to form uranium oxide. Understanding the rate of fluorine loss in uranium oxyfluoride particles, and the parameters that control it, may therefore contribute to placing boundaries on the particle's exposure time in the environment. Expressly for the purpose of this study, we prepared a set of uranium oxyfluoride particles at the Institute for Reference Materials and Measurements (EU-JRC-IRMM) from a static release of UF{sub 6} in a humid atmosphere. The majority of the samples was stored in controlled temperature, humidity and lighting conditions. Single particles were characterized by a suite of micro-analytical techniques, including NanoSIMS, micro-Raman spectrometry (MRS), scanning (SEM) and transmission (TEM) electron microscopy, energy-dispersive X-ray spectrometry (EDX) and focused ion beam (FIB). The small particle size was found to be the main analytical challenge. The relative amount of fluorine, as well as the particle chemical composition and morphology were determined at

  16. Uranium Mobility in Sediments From the 300 Area of the Hanford Site

    Science.gov (United States)

    Brown, C. F.; Serne, R. J.; Pierce, E. M.; Lindberg, M. J.

    2001-12-01

    The Hanford Site, located in South-Eastern Washington, was once home to cold war weapons grade plutonium production. Over the last ten years, the Site has shifted from production and operation to clean up and decontamination. One legacy still remaining at the Hanford Site is the 300 Area North Process Pond, which was used to treat industrial waste byproducts of the uranium fuel processing operation. More than ten thousand pounds of uranium have been recovered from the pond, yet contamination has still been found in the soils and groundwater beneath and around the Pond. The principle risk of this contamination is to groundwater in the 300 Area, where contaminant plumes are known to exceed applicable maximum contaminant levels. Previous studies report highly variable leach rates that appear to be a function of site-specific conditions and parameters. These parameters include: soil grain size and distribution, soil pH, EC, moisture content, organic matter, as well as mineralogical composition. A site-specific laboratory study was performed to determine uranium leach rates and adsorption-desorption partition coefficients for various sediments collected in and around the North Process Pond. Column tests involving saturated flow yielded sediment/sample specific U leach rates. Uranium concentrations in solution varied by as much as three orders of magnitude between sediment samples. Additional sediment characterization studies, including semi-selective extractions and x-ray absorption spectroscopy of size separates, are being conducted to determine if uranium solid-phase speciation can be measured/inferred and responsible for leach rate differences. These data and the site-specific leachates will be used to perform batch and column adsorption-desorption experiments, ultimately enabling us to predict partition coefficients/retardation factors for U under various future conditions and land use options.

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

    Energy Technology Data Exchange (ETDEWEB)

    Francis, C. W.

    1993-09-01

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

  18. 31 CFR 540.315 - Uranium-235 (U235).

    Science.gov (United States)

    2010-07-01

    ... 31 Money and Finance: Treasury 3 2010-07-01 2010-07-01 false Uranium-235 (U235). 540.315 Section... FOREIGN ASSETS CONTROL, DEPARTMENT OF THE TREASURY HIGHLY ENRICHED URANIUM (HEU) AGREEMENT ASSETS CONTROL REGULATIONS General Definitions § 540.315 Uranium-235 (U235). The term uranium-235 or U235 means the fissile...

  19. Dynamics of uranium vein mineralization

    Energy Technology Data Exchange (ETDEWEB)

    Petrosyan, R.V. (Ministerstvo Geologii SSR, Moscow)

    1981-01-01

    The formation of uraniun vein deposits and the essence of consanguinity of the mineralization and wall metasomatites are considered. The formation of uranium mineralization is analysed from the positions of Korzhinsky D. S. : the formation of metasomatite aureole and associated vein ores take place as a result of the development of one solution flow while the formation of mineral vein associations occurs on the background of continuous filtration of the solution during metasomato is due to a repeated (pulse) half-opening of fractures and their filling with a part of filtrating solution. The analysis of the available information on the example of two different uranium manifestations permits to reveal certain relations both in the character of wall rock alterations and between the metasomatosis and the formation of ore minerals in veins. The conclusion is made that spatial-time correlations of vein formations with wall metasomatites attest that the pulse formation of ores in veinlets occurs on the background and in interrelation with a consecutive precipitation of components in the aureole volume. The analysis of element migration dynamics in wall aureole carried out from the positions of the Korzhinsky hypothesis of the advance wave of acid components that takes into account the interaction of continuous and pulse mechanisms of solution movement permits to avoid contradictions when interpreting the processes of wall rock alterations and vein ore-forming, and permits to make a common scheme of vein ore-genesis.

  20. Uranium Pyrophoricity Phenomena and Prediction

    Energy Technology Data Exchange (ETDEWEB)

    DUNCAN, D.R.

    2000-04-20

    We have compiled a topical reference on the phenomena, experiences, experiments, and prediction of uranium pyrophoricity for the Hanford Spent Nuclear Fuel Project (SNFP) with specific applications to SNFP process and situations. The purpose of the compilation is to create a reference to integrate and preserve this knowledge. Decades ago, uranium and zirconium fires were commonplace at Atomic Energy Commission facilities, and good documentation of experiences is surprisingly sparse. Today, these phenomena are important to site remediation and analysis of packaging, transportation, and processing of unirradiated metal scrap and spent nuclear fuel. Our document, bearing the same title as this paper, will soon be available in the Hanford document system [Plys, et al., 2000]. This paper explains general content of our topical reference and provides examples useful throughout the DOE complex. Moreover, the methods described here can be applied to analysis of potentially pyrophoric plutonium, metal, or metal hydride compounds provided that kinetic data are available. A key feature of this paper is a set of straightforward equations and values that are immediately applicable to safety analysis.

  1. Occupational exposure to uranium particles

    Energy Technology Data Exchange (ETDEWEB)

    Carneiro, L.; Medeiros, G.; Dias da Cunha, K. [Instituto de Radioprotecao e Dosimetria (IRD/CNEN), Rio de Janeiro, RJ (Brazil)]. E-mail: carneiro@ird.gov.br; Lima, C.; Barros Leite, C.V.; Ramos, J.L. [Pontificia Universidade Catolica do Rio de Janeiro (PUC-RIO), RJ (Brazil). Dept. de Fisica

    2007-07-01

    The risk for the human health due to exposure to aerosols containing uranium depend on the intake pattern, the mass concentration and the speciation of the elements present in airborne particles. In this work PIXE (Particle Induced X ray Emission) technique was used to characterize aerosols samples collected in the environment. The PIXE technique allows the identification of the elements present in the sample and to determine their mass concentrations. The aerosol samples were collected using a six-stage cascade impactor and coarse and fine air sampler (AGF sampler) in two sites of Rio de Janeiro City. One, a mineral laboratory processing mineral containing uranium associated to crystals lattice located at Fundao Island a industrial zone and the other, in a laboratory at Barra da Tijuca a residential zone close to a lagoon and to the seashore. The Mass Median Aerodynamic Diameter (MMAD) measured indicated that the airborne particulate were in the fine fraction of the aerosols collected in both locations. In order to identify the contribution of the seawater particles from the Guanabara Bay in the aerosols, seawater samples were also collected at Fundao Island. The analysis of the results suggests that the aerosols are different in both sampling site and also exist a contribution from the Guanabara Bay seawater particles to the aerosols collected in the Fundao Island. (author)

  2. Uranium Detection - Technique Validation Report

    Energy Technology Data Exchange (ETDEWEB)

    Colletti, Lisa Michelle [Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Chemistry Division; Garduno, Katherine [Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Chemistry Division; Lujan, Elmer J. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Chemistry Division; Mechler-Hickson, Alexandra Marie [Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Chemistry Division; Univ. of Wisconsin, Madison, WI (United States); May, Iain [Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Chemistry Division; Reilly, Sean Douglas [Los Alamos National Lab. (LANL), Los Alamos, NM (United States). Chemistry Division

    2016-04-14

    As a LANL activity for DOE/NNSA in support of SHINE Medical Technologies™ ‘Accelerator Technology’ we have been investigating the application of UV-vis spectroscopy for uranium analysis in solution. While the technique has been developed specifically for sulfate solutions, the proposed SHINE target solutions, it can be adapted to a range of different solution matrixes. The FY15 work scope incorporated technical development that would improve accuracy, specificity, linearity & range, precision & ruggedness, and comparative analysis. Significant progress was achieved throughout FY 15 addressing these technical challenges, as is summarized in this report. In addition, comparative analysis of unknown samples using the Davies-Gray titration technique highlighted the importance of controlling temperature during analysis (impacting both technique accuracy and linearity/range). To fully understand the impact of temperature, additional experimentation and data analyses were performed during FY16. The results from this FY15/FY16 work were presented in a detailed presentation, LA-UR-16-21310, and an update of this presentation is included with this short report summarizing the key findings. The technique is based on analysis of the most intense U(VI) absorbance band in the visible region of the uranium spectra in 1 M H2SO4, at λmax = 419.5 nm.

  3. Reconnaissance soil geochemistry at the Riverton Uranium Mill Tailings Remedial Action Site, Fremont County, Wyoming

    Science.gov (United States)

    Smith, David B.; Sweat, Michael J.

    2012-01-01

    Soil samples were collected and chemically analyzed from the Riverton Uranium Mill Tailings Remedial Action Site, which lies within the Wind River Indian Reservation in Fremont County, Wyoming. Nineteen soil samples from a depth of 0 to 5 centimeters were collected in August 2011 from the site. The samples were sieved to less than 2 millimeters and analyzed for 44 major and trace elements following a near-total multi-acid extraction. Soil pH was also determined. The geochemical data were compared to a background dataset consisting of 160 soil samples previously collected from the same depth throughout the State of Wyoming as part of another ongoing study by the U.S. Geological Survey. Risk from potentially toxic elements in soil from the site to biologic receptors and humans was estimated by comparing the concentration of these elements with soil screening values established by the U.S. Environmental Protection Agency. All 19 samples exceeded the carcinogenic human health screening level for arsenic in residential soils of 0.39 milligrams per kilogram (mg/kg), which represents a one-in-one-million cancer risk (median arsenic concentration in the study area is 2.7 mg/kg). All 19 samples also exceeded the lead and vanadium screening levels for birds. Eighteen of the 19 samples exceeded the manganese screening level for plants, 13 of the 19 samples exceeded the antimony screening level for mammals, and 10 of 19 samples exceeded the zinc screening level for birds. However, these exceedances are also found in soils at most locations in the Wyoming Statewide soil database, and elevated concentrations alone are not necessarily cause for alarm. Uranium and thorium, two other elements of environmental concern, are elevated in soils at the site as compared to the Wyoming dataset, but no human or ecological soil screening levels have been established for these elements.

  4. Thorium (IV) toxicity of green microalgae from Scenedesmus and Monoraphidium genera; Toxicidade do torio (IV) para microalgas verdes dos generos Monoraphidium e Scenedesmus

    Energy Technology Data Exchange (ETDEWEB)

    Queiroz, Juliana Cristina de

    2009-07-01

    The toxicity of thorium by two green microalgae species, Monoraphidium sp. and Scenedesmus sp was studied. During the toxicity tests, the microalgae cultures were inoculated in ASM-I culture medium in the presence and absence of thorium (cultures at pH 8.0 and 6.0 in the absence of thorium, - control - and at pH 6.0 for thorium concentrations ranging from 0.5 to 100.0 mg/L Th). Its effect was monitored by direct counting on Fuchs-Rosenthal chamber and with the help of software developed by the group during the experiments. The difference in pH value in the culture medium did not affect the growth of the microalgae, and pH 6.0 was chosen as a reference in order not to compromise solubility and speciation of thorium in solution. The toxicity of the metal over the species was observed just for thorium concentrations over 50.0 mg/L. A Monoraphidium sp. culture containing 6.25x10{sup 5} microorganisms/mL reached a final concentration of 5.52x10{sup 7} microorganisms/mL in the presence of thorium in the concentration of 10.0 mg/L. If we consider the 100.0 ppm thorium solution reached a final concentration of 8.57x10{sup 6} microorganisms/mL. Control tests indicated a final concentration of 2.51x10{sup 7} microorganisms/mL at the end of the growth. Scenedesmus sp. cells proved to be more resistant to the presence of thorium in solution. Low concentrations of the radionuclide favored the growth of these microalgae. A culture containing 7.65x10{sup 5} microorganisms/mL reached a final concentration of 2.25x10{sup 6} microorganisms/mL, in the absence of thorium in the medium. Toxicological tests indicated a final culture concentration of 5.87x10{sup 6} microorganisms/mL in the presence of 0.5 mg/L thorium. The software used for comparison of direct count method proved to be very useful for the improvement of accuracy of the results obtained and a decrease in the uncertainty in counting. Beyond these advantages it also allowed recording of the data. From the present results

  5. Effects of Te(IV) Oxo-Anion Incorporation into Thorium Molybdates and Tungstates.

    Science.gov (United States)

    Xiao, Bin; Klinkenberg, Martina; Bosbach, Dirk; Suleimanov, Evgeny V; Alekseev, Evgeny V

    2015-06-15

    The exploration of phase formation in the Th-Mo/W-Te systems has resulted in four mixed oxo-anion compounds from high-temperature solid-state reactions: ThWTe2O9, Th(WO4)(TeO3), ThMoTe2O9, and Th2(MoO4)(TeO3)3. All four compounds contain edge-sharing thorium polyhedra linked by MoO4/WO6 and different tellurium oxo-groups to form three-dimensional frameworks. In ThWTe2O9, each helical Th based chain is connected by four tungstotellurite clusters resulting in a building fragment which has a cross-section of four-leafed clovers. The structure of Th(WO4)(TeO3) exhibits a multilayer-sandwich framework composed of thorium tellurite layers with tungsten chains in between. In the case of the molybdate family, ThMoTe2O9 and Th2(MoO4)(TeO3)3 are built from puckered Th-Te sheets which are further interconnected by MoO4 tetrahedral linkers. The DSC-TG technique was performed to gain insight into the thermal behavior of the synthesized compounds. Raman spectra of as-prepared phases were obtained and analyzed for signature peaks.

  6. Thorium cycle and molten salt reactors: field parameters and field constraints investigations toward 'thorium molten salt reactor' definition; Cycle thorium et reacteurs a sel fondu: exploration du champ des parametres et des contraintes definissant le 'Thorium Molten Salt Reactor'

    Energy Technology Data Exchange (ETDEWEB)

    Mathieu, L

    2005-09-15

    Producing nuclear energy in order to reduce the anthropic CO{sub 2} emission requires major technological advances. Nuclear plants of 4. generation have to respond to several constraints, as safety improvements, fuel breeding and radioactive waste minimization. For this purpose, it seems promising to use Thorium Cycle in Molten Salt Reactors. Studies on this domain have already been carried out. However, the final concept suffered from serious issues and was discontinued. A new reflection on this topic is being led in order to find acceptable solutions, and to design the Thorium Molten Salt Reactor concept. A nuclear reactor is simulated by the coupling of a neutron transport code with a materials evolution code. This allows us to reproduce the reactor behavior and its evolution all along its operation. Thanks to this method, we have studied a large number of reactor configurations. We have evaluated their efficiency through a group of constraints they have to satisfy. This work leads us to a better understanding of many physical phenomena controlling the reactor behavior. As a consequence, several efficient configurations have been discovered, allowing the emergence of new points of view in the research of Molten Salt Reactors. (author)

  7. Thorium-232 exposure during tungsten inert gas arc welding and electrode sharpening.

    Science.gov (United States)

    Saito, Hiroyuki; Hisanaga, Naomi; Okada, Yukiko; Hirai, Shoji; Arito, Heihachiro

    2003-07-01

    To assess the exposure of welders to thorium-232 (232Th) during tungsten inert gas arc (TIG) welding, airborne concentrations of 232Th in the breathing zone of the welder and background levels were measured. The radioactive concentrations were 1.11 x 10(-2) Bq/m3 during TIG welding of aluminum (TIG/Al), 1.78 x 10(-4) Bq/m3 during TIG welding of stainless steel (TIG/SS), and 1.93 x 10(-1) Bq/m3 during electrode sharpening, with 5.82 x 10(-5) Bq/m3 background concentration. Although the annual intake of 232Th estimated using these values did not exceed the annual limit intake (ALI, 1.6 x 10(2) Bq), we recommend reducing 232Th exposure by substituting thoriated electrodes with a thorium-free electrodes, setting up local ventilation systems, and by using respiratory protective equipment. It is also necessary to inform workers that thoriated tungsten electrodes contain radioactive material.

  8. Transmutation Strategy Using Thorium-Reprocessed Fuel ADS for Future Reactors in Vietnam

    Directory of Open Access Journals (Sweden)

    Thanh Mai Vu

    2013-01-01

    Full Text Available Nuclear power is believed to be a key to the energy security for a developing country like Vietnam where the power demanding increases rapidly every year. Nevertheless, spent nuclear fuel from nuclear power plants is the source of radiotoxic and proliferation risk. A conceptual design of ADS utilizing thorium fuel as a based fuel and reprocessed fuel as a seed for nuclear waste transmutation and energy production is proposed as one of the clean, safe, and economical solutions for the problem. In the design, 96 seed assemblies and 84 blanket assemblies were inserted into the core to make a heterogeneous subcritical core configuration. Introducing thorium fuel into the core offers an effective way to transmute plutonium and minor actinide (MA and gain energy from this process. Transmutation rate as a function of burnup is estimated using MCNPX 2.7.0 code. Results show that by using the seed-blanket designed ADS, at 40 GWd/t burnup, 192 kg of plutonium and 156 kg of MA can be eliminated. Equivalently, 1  ADS can be able to transmute the transuranic (TRU waste from 2  LWRs. 14 units of ADS would be required to eliminate TRUs from the future reactors to be constructed in Vietnam.

  9. Feasibility of Thorium Fuel Cycles in a Very High Temperature Pebble-Bed Hybrid System

    Directory of Open Access Journals (Sweden)

    L.P. Rodriguez

    2015-08-01

    Full Text Available Nuclear energy presents key challenges to be successful as a sustainable energy source. Currently, the viability of the use thorium-based fuel cycles in an innovative nuclear energy generation system is being investigated in order to solve these key challenges. In this work, the feasibility of three thorium-based fuel cycles (232Th-233U, 232Th-239Pu, and 232Th-U in a hybrid system formed by a Very High Temperature Pebble-Bed Reactor (VHTR and two Pebble-Bed Accelerator Driven Systems (ADSs was evaluated using parameters related to the neutronic behavior such as nuclear fuel breeding, minor actinide stockpile, the energetic contribution of each fissile isotope, and the radiotoxicity of the long lived wastes. These parameters were used to compare the fuel cycles using the well-known MCNPX ver. 2.6e computational code. The results obtained confirm that the 232Th-233U fuel cycle is the best cycle for minimizing the production of plutonium isotopes and minor actinides. Moreover, the inclusion of the second stage in the ADSs demonstrated the possibility of extending the burnup cycle duration and reducing the radiotoxicity of the discharged fuel from the VHTR.

  10. Numerical studies of acceleration of thorium ions by a laser pulse of ultra-relativistic intensity

    Science.gov (United States)

    Domanski, Jaroslaw; Badziak, Jan

    2018-01-01

    One of the key scientific projects of ELI-Nuclear Physics is to study the production of extremely neutron-rich nuclides by a new reaction mechanism called fission-fusion using laser-accelerated thorium (232Th) ions. This research is of crucial importance for understanding the nature of the creation of heavy elements in the Universe; however, they require Th ion beams of very high beam fluencies and intensities which are inaccessible in conventional accelerators. This contribution is a first attempt to investigate the possibility of the generation of intense Th ion beams by a fs laser pulse of ultra-relativistic intensity. The investigation was performed with the use of fully electromagnetic relativistic particle-in-cell code. A sub-μm thorium target was irradiated by a circularly polarized 20-fs laser pulse of intensity up to 1023 W/cm2, predicted to be attainable at ELI-NP. At the laser intensity 1023 W/cm2 and an optimum target thickness, the maximum energies of Th ions approach 9.3 GeV, the ion beam intensity is > 1020 W/cm2 and the total ion fluence reaches values 1019 ions/cm2. The last two values are much higher than attainable in conventional accelerators and are fairly promising for the planned ELI-NP experiment.

  11. India's Worsening Uranium Shortage

    Energy Technology Data Exchange (ETDEWEB)

    Curtis, Michael M.

    2007-01-15

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

  12. Technical Basis for Assessing Uranium Bioremediation Performance

    Energy Technology Data Exchange (ETDEWEB)

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

    2008-04-01

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

  13. Development of separation technology for the removal of radium-223 from targeted thorium conjugate formulations. Part I: purification of decayed thorium-227 on cation exchange columns.

    Science.gov (United States)

    Frenvik, Janne Olsen; Dyrstad, Knut; Kristensen, Solveig; Ryan, Olav B

    2017-02-01

    Targeted thorium conjugates (TTCs) are being explored as a potential future platform for specific tumor targeting pharmaceuticals. In TTCs, the alpha emitting radionuclide thorium-227 ((227)Th) with a half-life of 18.697 d is labeled to targeting moieties, such as monoclonal antibodies (mAbs). The amount of daughter nuclide radium-223 ((223)Ra, t1/2 = 11.435 d) will increase during manufacture and distribution, and so a technology for purification is required to assure an acceptable level of (223)Ra is administrated to the patient. Since (223)Ra is the only progeny of (227)Th with a long half-life (days), the progenies of (223)Ra will have a very limited stay in the formulation once (223)Ra is removed. The focus in this study has, therefore, been on the removal of (223)Ra. In this study, the sorption and separation of (223)Ra (radium(II)) and (227)Th (thorium(IV)) on cation exchange columns has been evaluated as a purification method of decayed (227)Th (i.e. prior to radiolabelling of a mAb and formation of TTC). The goal is to minimize the sorption of (227)Th and maximize the sorption of (223)Ra. Statistical experimental design with formulation and process parameters, including buffered formulations comprising citrate and acetate, at various concentrations and pH, presence of free radical scavenger and chelator, and resin amount have been evaluated for impact on the purification process. The studies have been interpreted by the aid of multivariate data analysis. The correlations between design of experimental variables and sorption are summarized by regression models. The predictive accuracy of radionuclide sorption was given by standard deviation and 95% confidence intervals originating from statistical cross validation. Experimental results and statistical models for citrate-buffered formulations verified reproducible and acceptable sorption levels of (223)Ra and (227)Th under selected conditions. For acetate-buffered formulations, prediction of (227)Th

  14. Capstone Depleted Uranium Aerosols: Generation and Characterization

    Energy Technology Data Exchange (ETDEWEB)

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

    2004-10-19

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

  15. Development of uranium processing at Wiluna

    Energy Technology Data Exchange (ETDEWEB)

    Kenny, D., E-mail: dayle.kenny@toroenergy.com.au [Toro Energy Ltd., West Perth, WA (Australia); Dombrose, E. [Metallurgical Support Pty Ltd., Shelley, WA (Australia)

    2010-07-01

    Toro Energy Ltd. has identified a resource of 20.2 million tonnes at a grade of 548 ppm U{sub 3}O{sub 8} at Wiluna, Western Australia. Calcrete and clay delta formations host the uranium mineral carnotite. Initial studies indicate a mining operation is technically, environmentally and commercially viable. Increase in demand for uranium and a change in State Government policy on uranium mining have lead Toro to proceed with a bankable feasibility study and commence approvals with State and Federal Governments. This paper discusses how Toro arrived at the decision to utilise alkaline heap leach, a process not widely used, and how it is being developed. (author)

  16. Development of separation technology for the removal of radium-223 from targeted thorium conjugate formulations. Part II: purification of targeted thorium conjugates on cation exchange columns.

    Science.gov (United States)

    Frenvik, Janne Olsen; Dyrstad, Knut; Kristensen, Solveig; Ryan, Olav B

    2017-09-01

    Tumor targeting pharmaceuticals will play a crucial role in future pharma pipelines. The targeted thorium conjugate (TTC) therapeutic platform could provide real benefit to patients, whereby targeting moieties like monoclonal antibodies are radiolabelled with the alpha-emitting radionuclide thorium-227 ((227)Th, t1/2 = 18.7 days). A potential problem could be the accumulation of the long-lived daughter nuclide radium-223 ((223)Ra, t1/2 = 11.4 days) in the drug product during manufacturing and distribution. Therefore, the level of (223)Ra must be standardized before administration to the patient. The focus in this study has been the removal of (223)Ra, as the other progenies will have a very limited stay in the formulation. In this study, the purification of TTCs labeled with decayed (227)Th has been explored. Columns packed with a strong cation exchange resin have been used to sequester (223)Ra. The separation of TTC from (223)Ra has been evaluated as influenced by both formulation and process parameters with a design of experiments (DOE) study; including citrate or acetate buffer, pH, buffer concentration, presence or absence of pABA + EDTA, resin amount and sodium chloride concentration. The aim was to achieve a separation with high sorption of (223)Ra and accompanying low TTC sorption. The results were analyzed by multivariate analysis. Four regression models of TTC and (223)Ra sorption from citrate and acetate buffered formulations were developed. The predictive accuracy of sorption in the four statistical models was given by standard deviations and confidence intervals. The TTC sorption in citrate and acetate buffered formulations was affected by the identical variables and the variation in TTC sorption was comparable for the two models. However, the DOE variables had a significantly stronger impact on the (223)Ra sorption in citrate buffered formulations than the (223)Ra sorption in acetate buffer. An optimal separation with a TTC sorption

  17. Evaluation of the effectiveness of the filtration leaching for uranium recovery from uranium ore

    Directory of Open Access Journals (Sweden)

    Bolat Uralbekov

    2015-09-01

    Full Text Available The physical and chemical processes taking place in filtration leaching of uranium from uranium ore sample by sulphuric acid solution have been studied by modern physico-chemical methods (X-ray diffraction, scanning electron spectroscopy, electron probe microanalysis, optical emission spectroscope, ICP OES. Column leaching test was carried out for ore samples obtained from a uranium in-situ leaching (ISL mining site using deluted sulphuricacid to study the evolution of various elements concentration in the pregnant leach solution. It has been shown that the uranium in pregnant solutions appears by dissolution of calcium and magnesium carbonates and uranium minerals as well. It was found the decreasing of filtration coefficient from 0.099 m day-1 to 0.082 m day-1, due to the presence of mechanical and chemical mudding. Partial extraction of uranium (85% from the ore has been explained by the slow diffusion of sulfuric acid to the uranium minerals locates in the cracks of silicate minerals. It was concluded that the studied uranium ore sample according to adverse geotechnical parameters is not suitable for uranium extraction by filtration leaching.

  18. Remedial action plan and site design for stabilization of the inactive uranium mill tailings site at Lakeview, Oregon: Volume 1, Text and appendices A through D

    Energy Technology Data Exchange (ETDEWEB)

    Chernoff, A R [USDOE Albuquerque Operations Office, NM (United States). Uranium Mill Tailings Project Office; Ervin, C [Oregon State Dept. of Energy, Salem, OR (United States)

    1992-07-01

    The Lakeview inactive uranium processing site is in Lake County, Oregon, approximately one mile northwest of the town of Lakeview, sixteen miles north of the California-Oregon border, and 96 miles east of Klamath Falls. The total designated site covers an area of 258 acres consisting of a tailings pile (30 acres). seven evaporation ponds (69 acres), the mill buildings, and related structures. The mill buildings and other structures have been decontaminated and are currently being used by Goose Lake Lumber Company. The tailings pile at the processing site was originally stabilized by Atlantic Richfield with an earthen cover 18--24 inches thick. The average depth of the tailings, including the cover, varied from six to eight feet. There were estimated to be 662,000 cubic yards of tailings, windblown contaminated materials, and vicinity property materials. During remedial action under the Uranium Mill Tailings Remedial Action (UMTRA) Project, approximately 264,000 cubic yards of additional contaminated materials were identified from excavations required to remove thorium- and arsenic-contaminated soils. The remedial action for the Lakeview site consisted of the cleanup, relocation, consolidation, and stabilization of all residual radioactive materials and thorium- and arsenic-contaminated materials in a partially below-grade disposal cell at a location approximately seven miles northwest of the tailings site, identified as the Collins Ranch site. A cover, including a radon/infiltration barrier and rock layer for protection from erosion, was Placed on top of the tailings. A rock-soil matrix covers the topslope and provides a growth medium for vegetation. The US Department of Energy (DOE) will retain the license and surveillance and maintenance responsibilities for the final restricted site of 13 acres.

  19. Model for the analysis of transitories and stability of a BWR reactor with fuel of thorium; Modelo para el analisis de transitorios y de estabilidad de un reactor BWR con combustible de torio

    Energy Technology Data Exchange (ETDEWEB)

    Nunez C, A. [CNSNS, 03020 Mexico D.F. (Mexico)]. E-mail: anunezc@cnsns.gob.mx; Espinosa P, G. [UAM-I, 09340 Mexico D.F. (Mexico); Francois L, J.L. [Fac. de Ingenieria, UNAM 62550 Jiutepec, Morelos (Mexico)

    2004-07-01

    In this work it is described the thermo hydraulic and neutronic pattern used to simulate the behavior of a nucleus of thorium-uranium under different conditions of operation. The analysed nucleus was designed with base to assemblies that operate under the cover-seed concept. The pattern was proven to conditions of stationary state and transitory state. Here it is only presented the simulation of the one SCRAM manual and it is compared in the behavior of a nucleus with UO{sub 2}. Additionally one carries out an analysis of stability taking into account the four corners that define the area of stability of the map flow-power and to conditions of 100% of flow and 100% of power. The module of stability is based on the pattern of Lahey and Podowsky to estimate the drops of pressure during a perturbation. It is concludes that the behavior of this nucleus is not very different to the one shown by the nuclei loaded with the fuel of UO{sub 2}. (Author)

  20. Measurement of the {sup 232}thorium capture cross section at n-TOF-CERN; Mesure de la section efficace de capture neutronique du {sup 232}Th a n-TOF au CERN

    Energy Technology Data Exchange (ETDEWEB)

    Aerts, G

    2005-09-01

    Within the context of nuclear power as a sustainable energy resource, a program of research is concentrated on a new nuclear fuel cycle based on thorium. The main advantage, as compared to the uranium cycle, is a lower production of minor actinides, of which the radiological impact on the long term constitutes a problem. At present, nuclear data libraries don't provide cross sections of a good enough quality, allowing more realistic calculations from simulations related to these reactors. The {sup 232}Th neutron capture cross section is an example. With the n-TOF collaboration, the measurement of this reaction was achieved in 2002 using two C{sub 6}D{sub 6} detectors. The experimental area located at CERN, is characterized by an outstanding neutron energy resolution coupled to a high instantaneous neutron flux. The determination of the gamma-ray cascade detection efficiency, with a random behaviour, has been obtained by the use of weighting functions. These were deduced from Monte Carlo simulations with the code MCNP. Data extraction, reduction, and the description of the neutron flux have lead to the capture yield. In the resolved resonance region, the resonance parameters describing the cross section were deduced with the code SAMMY, using the R-matrix theory. In the unresolved resonance region, an uncertainty of 3,5% is found, and a comparison with recent measurements shows a good agreement. (author)

  1. Mountain wetlands: efficient uranium filters - potential impacts

    Science.gov (United States)

    Owen, D.E.; Otton, J.K.

    1995-01-01

    Sediments in 67 of 145 Colorado wetlands sampled by the US Geological Survey contain moderate (20 ppm) or greater concentrations of uranium (some as high as 3000 ppm) based on dry weight. The proposed maximum contaminant level (MCL) for uranium in drinking water is 20 ??g/l or 20 ppb. By comparison, sediments in many of these wetlands contain 3 to 5 orders of magnitude more uranium than the proposed MCL. Wetlands near the workings of old mines may be trapping any number of additional metals/elements including Cu, Pb, Zn, As and Ag. Anthropogenic disturbances and natural changes may release uranium and other loosely bound metals presently contained in wetland sediments. -from Authors

  2. Treatment of effluents from uranium oxide production.

    Science.gov (United States)

    Ladeira, A C Q; Gonçalves, J S; Morais, C A

    2011-01-01

    The nuclear fuel cycle comprises a series of industrial processes which involve the production of electricity from uranium in nuclear power reactors. In Brazil the conversion of uranium hexafluoride (UF6) into uranium dioxide (UO2) takes place in Resende (RJ) at the Nuclear Fuel Factory (FCN). The process generates liquid effluents with significant concentrations of uranium, which might be treated before being discharged into the environment. This study investigates the recovery of uranium from three distinct liquid effluents: one with a high carbonate content and the other with an elevated fluoride concentration. This paper also presents a study on carbonate removal from an effluent that consists of a water-methanol solution generated during the filtration of the yellow cake (ammonium uranyl tricarbonate). The results showed that: (1) the uranium from the carbonated solution can be recovered through the ion exchange technique using the strong base anionic resin IRA 910-U, as the carbonate has been removed as CO2 after heating; (2) the most suitable technique to recover uranium from the fluoride solution is its precipitation as (NH4)2UO4F2 (ammonium fluorouranate peroxide), (3) the solution free of carbonate can be added to the fluoride solution and the uranium from the final solution can be recovered by precipitation as ammonium fluorouranate peroxide as well; (4) the carbonate from the water-methanol solution can be recovered as calcium carbonate through the addition of calcium chloride, or it can be recovered as ammonium sulphate through the addition of sulphuric acid. The ammonium sulphate product can be used as a fertilizer.

  3. FABRICATION OF URANIUM-ALUMINUM ALLOYS

    Science.gov (United States)

    Saller, H.A.

    1959-12-15

    A process is presented for producing a workable article of a uranium- aluminum alloy in which the uranium content is between 14 and 70% by weight; aluminum powder and powdered UAl/sub 2/, UAl/sub 3/, UAl/sub 5/, or UBe/sub 9/ are mixed, and the mixture is compressed into the shape desired and sintered at between 450 and 600 deg C.

  4. The ultimate disposition of depleted uranium

    Energy Technology Data Exchange (ETDEWEB)

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

    1991-12-31

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

  5. Pentavalent uranium trans-dihalides and -pseudohalides.

    Science.gov (United States)

    Lewis, Andrew J; Nakamaru-Ogiso, Eiko; Kikkawa, James M; Carroll, Patrick J; Schelter, Eric J

    2012-05-21

    Pentavalent uranium complexes of the formula U(V)X(2)[N(SiMe(3))(2)](3) (X = F(-), Cl(-), Br(-), N(3)(-), NCS(-)) are accessible from the oxidation of U(III)[N(SiMe(3))(2)](3) through two sequential, one-electron oxidation reactions (halides) and substitution through salt metathesis (pseudohalides). Uranium(v) mixed-halides are also synthesized by successive one-electron oxidation reactions.

  6. Multifactorial Assessment of Depleted Uranium Neurotoxicity

    Science.gov (United States)

    2006-12-01

    Changes in sleep - wake cycle after chronic exposure to uranium in rats. Neurotoxicol Teratol 27: 835-40. Lestaevel, P., P. Houpert, C. Bussy, B...delivery to 43muscle and brain, acute stimulation of immune function, and 44sharpened cognition with increased cerebral glucose utilization . 45While...procedures. Inductively coupled plasma-mass spectrometry (ICP-MS) analysis was used to assess the kinetics of uranium in the cerebral cortex, hippocampus

  7. PROCESSES OF CHLORINATION OF URANIUM OXIDES

    Science.gov (United States)

    Rosenfeld, S.

    1958-09-16

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

  8. Kinetics of thorium and particle cycling along the U.S. GEOTRACES North Atlantic Transect

    Science.gov (United States)

    Lerner, Paul; Marchal, Olivier; Lam, Phoebe J.; Buesseler, Ken; Charette, Matthew

    2017-07-01

    The high particle reactivity of thorium has resulted in its widespread use in tracing processes impacting marine particles and their chemical constituents. The use of thorium isotopes as tracers of particle dynamics, however, largely relies on our understanding of how the element scavenges onto particles. Here, we estimate apparent rate constants of Th adsorption (k1), Th desorption (k-1), bulk particle degradation (β-1), and bulk particle sinking speed (w) along the water column at 11 open-ocean stations occupied during the GEOTRACES North Atlantic Section (GA03). First, we provide evidence that the budgets of Th isotopes and particles at these stations appear to be generally dominated by radioactive production and decay sorption reactions, particle degradation, and particle sinking. Rate parameters are then estimated by fitting a Th and particle cycling model to data of dissolved and particulate 228,230,234Th, 228Ra, particle concentrations, and 234,238U estimates based on salinity, using a nonlinear programming technique. We find that the adsorption rate constant (k1) generally decreases with depth across the section: broadly, the time scale 1 /k1 averages 1.0 yr in the upper 1000 m and (1.4-1.5) yr below. A positive relationship between k1 and particle concentration (P) is found, i.e., k1 ∝Pb , where b ≥ 1 , consistent with the notion that k1 increases with the number of surface sites available for adsorption. The rate constant ratio, K =k1 / (k-1 +β-1) , which measures the collective influence of rate parameters on Th scavenging, averages 0.2 for most stations and most depths. We clarify the conditions under which K / P is equivalent to the distribution coefficient, KD, test that the conditions are met at the stations, and find that K / P decreases with P, in line with a particle concentration effect (dKD / dP concentration effect arises from the joint effect of P on the rate constants for thorium attachment to, and detachment from, particles.

  9. [Biosorption of Radionuclide Uranium by Deinococcus radiodurans].

    Science.gov (United States)

    Yang, Jie; Dong, Fa-qin; Dai, Qun-wei; Liu, Ming-xue; Nie, Xiao-qin; Zhang, Dong; Ma, Jia-lin; Zhou, Xian

    2015-04-01

    As a biological adsorbent, Living Deinococcus radiodurans was used for removing radionuclide uranium in the aqueous solution. The effect factors on biosorption of radionuclide uranium were researched in the present paper, including solution pH values and initial uranium concentration. Meanwhile, the biosorption mechanism was researched by the method of FTIR and SEM/EDS. The results show that the optimum conditions for biosorption are as follows: pH = 5, co = 100 mg · L(-1) and the maximum biosorption capacity is up to 240 mgU · g(-1). According to the SEM results and EDXS analysis, it is indicated that the cell surface is attached by lots of sheet uranium crystals, and the main biosorpiton way of uranium is the ion exchange or surface complexation. Comparing FTIR spectra and FTIR fitting spectra before and after biosorption, we can find that the whole spectra has a certain change, particularly active groups (such as amide groups of the protein, hydroxy, carboxyl and phosphate group) are involved in the biosorption process. Then, there is a new peak at 906 cm(-1) and it is a stretching vibration peak of UO2(2+). Obviously, it is possible that as an anti radiation microorganism, Deinococcus radiodurans could be used for removing radionuclide uranium in radiation environment.

  10. Whole-organism concentration ratios in wildlife inhabiting Australian uranium mining environments

    Energy Technology Data Exchange (ETDEWEB)

    Hirth, Gillian A.; Carpenter, Julia G. [Australian Radiation Protection and Nuclear Safety Agency, 619 Lower Plenty Rd, Yallambie, 3085, Victoria (Australia); Bollhoefer, Andreas [Environmental Research Institute of the Supervising Scientist, GPO Box 461, Darwin, 0801 Northern Territory (Australia); Johansen, Mathew P. [Australian Nuclear Science and Technology Organisation, Locked Bag 2001, Kirrawee, DC, NSW 2232 (Australia); Beresford, Nicholas A. [NERC Centre for Ecology and Hydrology, Bailrigg, Lancaster LA1 4AP (United Kingdom)

    2014-07-01

    Environmental impact assessments conducted for Australian mine sites involving naturally occurring radioactive material require an assessment of radiation doses to wildlife. Whole-organism concentration ratios (CR{sub wo}) are pivotal in these assessments and previous reviews have identified a need for a more complete and consolidated database of Australian-specific CR{sub wo} that could be used. Concern had also been expressed by some stakeholders in Australia about the suitability of the default CR{sub wo} values provided in standard biota dose models (e.g., ERICA Tool, RESRAD-BIOTA, ICRP framework) for Australian wildlife and environmental conditions. In order to address these concerns and support the implementation of best-practice standards in environmental radiological assessment, the Australian Radiation Protection and Nuclear Safety Agency (ARPANSA), with support from the Department of Resources, Energy and Tourism (RET), undertook an evaluation of existing data relating to wildlife inhabiting Australian uranium mining environments. CR{sub wo} values were calculated using data from a range of original sources. These included scientific journal publications, technical reports from Australian government organisations, site-specific data from mining operators and data from baseline environmental surveys undertaken during the 1970's and 1980's. The Australian data previously included in the international Wildlife Transfer Database (WTD, www.wildlifetransferdatabase.org) were also reviewed and updated. This paper discusses the data analysis process and associated uncertainties. CR{sub wo} values are reported for uranium, thorium, radium-226, lead-210 and polonium-210 for a range of endemic and introduced wildlife, with a focus on plants and animals from both terrestrial and freshwater environments where uranium mining has been proposed or undertaken. This has resulted in the calculation of more than 500 CR{sub wo} values for inclusion in the database

  11. Use of uranium isotopes as a temporal and spatial tracer of nuclear contamination in the environment.

    Science.gov (United States)

    Tortorello, R; Widom, E; Renwick, W H

    2013-10-01

    The Fernald Feed Materials Production Center (FFMPC) was established in 1951 to process natural uranium (U) ore, enriched uranium (EU) and depleted uranium (DU). This study tests the utility of U isotopic ratios in sediment cores and lichens as indicators of the aerial extent, degree and timing of anthropogenic U contamination, using the FFMPC as a test case. An 80-cm-long sediment core was extracted from an impoundment located approximately 6.7 km southwest of the FFMPC. Elemental concentrations of thorium (2.7-6.2 μg g(-1)) and U (0.33-1.33 μg g(-1)) as well as major and minor U isotopes were analyzed in the core. The lack of measurable (137)Cs in the deepest sample as well as a natural (235)U/(238)U signature and no measurable (236)U, are consistent with pre-FFMPC activity. Anomalously elevated U with respect to Th concentrations occur in seven consecutive samples immediately above the base of the core (62-76 cm depth). Samples with elevated U concentrations also show variable (235)U/(238)U (0.00645-0.00748), and all contain measurable (236)U ((236)U/(238)U = 2.1 × 10(-6)-3.6 × 10(-5)). Correspondence between the known releases of U dust from the FFMPC through time and variations in sediment core U concentrations, (235)U/(238)U and (236)U/(238)U ratios provide evidence for distinct releases of both DU and EU. Furthermore, these relationships demonstrate that the sediment core serves as a robust archive of past environmental U contamination events. Samples in the upper 40 cm display natural (235)U/(238)U, but measurable (236)U/(238)U ((236)U/(238)U = 5.68 × 10(-6)-1.43 × 10(-5)), further indicating the continued presence of anthropogenic U in present-day sediment. Three local lichen samples were also analyzed, and all display either EU or DU signatures coupled with elevated (236)U/(238)U, recording airborne U contamination from the FFMPC. Copyright © 2013 Elsevier Ltd. All rights reserved.

  12. Measurements of Fission Cross Sections for the Isotopes relevant to the Thorium Fuel Cycle

    CERN Multimedia

    2002-01-01

    The present concern about a sustainable energy supply is characterised by a considerable uncertainty: the green house effect and foreseeable limits in fossil fuel resources on the one hand, the concern about the environmental impact of nuclear fission energy and the long term fusion research on the other hand, have led to the consideration of a variety of advanced strategies for the nuclear fuel cycle and related nuclear energy systems. The present research directories concern such strategies as the extension of the life span of presently operating reactors, the increase of the fuel burn-up, the plutonium recycling, and in particular the incineration of actinides and long-Lived fission products, the accelerator driven systems (ADS), like the "Energy Amplifier" (EA) concept of C. Rubbia, and the possible use of the Thorium fuel cycle. The detailed feasibility study and safety assessment of these strategies requires the accurate knowledge of neutron nuclear reaction data. Both, higher fuel burn-up and especiall...

  13. Removal of thorium(IV) from aqueous solutions by natural sepiolite

    Energy Technology Data Exchange (ETDEWEB)

    Erden, Kadriye Esen [Pamukkale Univ., Denizli (Turkey). Dept. of Electricity and Energy; Donat, Ramazan [Pamukkale Univ., Denizli (Turkey). Dept. of Chemistry

    2017-06-01

    Natural sepiolite has been tested as a potential sorbent for the removal of Th(IV) from aqueous solutions by batch technique. Effects of various parameters on the adsorption process have been investigated. Under optimum conditions, Th(IV) was adsorbed with high adsorption efficiency. The results indicated that sorption of Th(IV) on sepiolite was strongly affected by pH values and temperature. The adsorption patterns of thorium on the sepiolite adsorbent followed the Langmuir, Freundlich and Dubinin-Radushkevich (D-R) isotherms. The thermodynamic data (ΔH , ΔS , ΔG ) are calculated from the temperature-dependent sorption isotherms. The results suggest that sorption process of Th(IV) on sepiolite is spontaneous and endothermic.

  14. Nuclear radii of thorium isotopes from laser spectroscopy of stored ions

    Energy Technology Data Exchange (ETDEWEB)

    Kaelber, W.; Rink, J.; Bekk, K.; Goering, S.; Meisel, G.; Rebel, H.; Faubel, W.; Thompson, R.C.

    1989-09-01

    Isotope shifts and hyperfine splittings in optical transitions for atomic ions of the thorium isotopes /sup 227/Th to /sup 230/Th and /sup 232/Th have been measured by laser spectroscopy on stored ions. From the isotope shift data, changes of the mean square charge radii are determined. A continuous increase of the charge radius with mass number A is observed, in agreement with droplet model calculations. The results indicate that the odd-even staggering for Th is different from that one of the neighbouring isotones of Fr and Ra. There is some empirical evidence from systematics for an inversion of the staggering and the appearance of an octupole deformation at N/le/137. The hyperfine splitting for /sup 229/Th for 3 electronic levels is given. (orig.).

  15. Influence of moderator to fuel ratio (MFR) on burning thorium in a subcritical assembly

    Energy Technology Data Exchange (ETDEWEB)

    Wojciechowski, Andrzej, E-mail: andrzej.wojciechowski@ncbj.gov.pl [National Center for Nuclear Research, Otwock-Swierk (Poland); Joint Institute for Nuclear Research, Dubna (Russian Federation)

    2014-10-15

    The conversion ratio (CR) of Th-232 to U-233 calculation results for a subcritical reactor assembly is presented as a function of MFR, burnup, power density (PD) and fissile concentration. The calculated model is based on subcritical assembly which makes configuration of fuel rods and volumes of moderator and coolant changes possible. This comfortable assembly enables investigation of CR in a thorium cycle for different value of MFR. Additionally, the calculation results of U-233 saturation concentration are explained by mathematical model. The value of MFR main influences the saturation concentration of U-233 and fissile and the fissile concentration dependence of CR. The saturation value of CR is included in the range CR ∈ (0.911, 0.966) and is a slowly increasing function of MFR. The calculations were done with a MCNPX 2.7 code.

  16. Simultaneous Separation of Actinium and Radium Isotopes from a Proton Irradiated Thorium Matrix.

    Science.gov (United States)

    Mastren, Tara; Radchenko, Valery; Owens, Allison; Copping, Roy; Boll, Rose; Griswold, Justin R; Mirzadeh, Saed; Wyant, Lance E; Brugh, Mark; Engle, Jonathan W; Nortier, Francois M; Birnbaum, Eva R; John, Kevin D; Fassbender, Michael E

    2017-08-15

    A new method has been developed for the isolation of (223,224,225)Ra, in high yield and purity, from a proton irradiated (232)Th matrix. Herein we report an all-aqueous process using multiple solid-supported adsorption steps including a citrate chelation method developed to remove >99.9% of the barium contaminants by activity from the final radium product. A procedure involving the use of three columns in succession was developed, and the separation of (223,224,225)Ra from the thorium matrix was obtained with an overall recovery yield of 91 ± 3%, average radiochemical purity of 99.9%, and production yields that correspond to physical yields based on previously measured excitation functions.

  17. High Efficiency Nuclear Power Plants Using Liquid Fluoride Thorium Reactor Technology

    Science.gov (United States)

    Juhasz, Albert J.; Rarick, Richard A.; Rangarajan, Rajmohan

    2009-01-01

    An overall system analysis approach is used to propose potential conceptual designs of advanced terrestrial nuclear power plants based on Oak Ridge National Laboratory (ORNL) Molten Salt Reactor (MSR) experience and utilizing Closed Cycle Gas Turbine (CCGT) thermal-to-electric energy conversion technology. In particular conceptual designs for an advanced 1 GWe power plant with turbine reheat and compressor intercooling at a 950 K turbine inlet temperature (TIT), as well as near term 100 MWe demonstration plants with TITs of 950 and 1200 K are presented. Power plant performance data were obtained for TITs ranging from 650 to 1300 K by use of a Closed Brayton Cycle (CBC) systems code which considered the interaction between major sub-systems, including the Liquid Fluoride Thorium Reactor (LFTR), heat source and heat sink heat exchangers, turbo-generator machinery, and an electric power generation and transmission system. Optional off-shore submarine installation of the power plant is a major consideration.

  18. Thorium utilization program. Quarterly progress report for the period ending May 31, 1977

    Energy Technology Data Exchange (ETDEWEB)

    1977-06-01

    Results of work performed under the National HTGR Fuel Recycle Program (also known as the Thorium Utilization Program) at General Atomic Company are presented. Results of work on this program prior to June 1974 were included in a quarterly series on the HTGR Base Program. The work reported includes the development of unit processes and equipment for reprocessing of High-Temperature Gas-Cooled Reactor (HTGR) fuel, the design and development of an integrated pilot line to demonstrate the head end of HTGR reprocessing using unirradiated fuel materials, and design work in support of Hot Engineering Tests (HET). Work is also described on trade-off studies concerning the required design of facilities and equipment for the large-scale recycle of HTGR fuels in order to guide the development activities for HTGR fuel recycle.

  19. Laser properties of holmium and erbium in thorium-, zinc- and yttrium-based fluoride glass

    Science.gov (United States)

    Eyal, M.; Reisfeld, R.; Jørgensen, C. K.; Bendow, B.

    Optical properties of Ho(III)- and Er(III)-doped thorium-, zinc- and yttrium-based fluoride glasses are determined. Due to the large number of luminescent levels, it is possible to determine the multiphonon relaxation rates even for energy gaps smaller than 1900 cm -. Peak cross sections for laser action and threshold powers for infrared laser emissions are calculated and compared with literature data. It is shown that addition of other lanthanides significantly decreases the threshold power for laser action. The results indicate that a rare-earth-doped fluoride glass is a promising candidate for an integrated fiber optics system in which the rare earth laser is a part of the fiber.

  20. Gas-cooled thorium reactor with fuel block of the unified design

    Directory of Open Access Journals (Sweden)

    I.V. Shamanin

    2015-11-01

    Analysis of information materials pertaining to the use of thorium as fuel element in rector facilities of the new generation and of its future potential was performed in the present study. Results of the first phase of neutronics studies of 3D model of high-temperatures gas-cooled reactor facility on the basis of unified design of the fuel block are presented. Calculation 3D model was developed using the software code of the MCU-5 series. Several optimal configurations of the reactor core were selected according to the results of comparison of neutronics characteristics of the examined options for the purpose of development of small-size modular nuclear power installations with power up to 60MW. Results of calculations of reactivity margin of the reactor, neutron flux distribution and power density profiles are presented for the selected options of reactor core configuration.

  1. Power level effects on thorium-based fuels in pressure-tube heavy water reactors

    Energy Technology Data Exchange (ETDEWEB)

    Bromley, B.P.; Edwards, G.W.R., E-mail: blair.bromley@cnl.ca [Canadian Nuclear Laboratories, Chalk River, Ontario (Canada); Sambavalingam, P. [Univ. of Ontario Inst. of Technology, Oshawa, Ontario (Canada)

    2016-06-15

    Lattice and core physics modeling and calculations have been performed to quantify the impact of power/flux levels on the reactivity and achievable burnup for 35-element fuel bundles made with Pu/Th or U-233/Th. The fissile content in these bundles has been adjusted to produce on the order of 20 MWd/kg burnup in homogeneous cores in a 700 MWe-class pressure-tube heavy water reactor, operating on a once-through thorium cycle. Results demonstrate that the impact of the power/flux level is modest for Pu/Th fuels but significant for U-233/Th fuels. In particular, high power/flux reduces the breeding and burnup potential of U-233/Th fuels. Thus, there may be an incentive to operate reactors with U-233/Th fuels at a lower power density or to develop alternative refueling schemes that will lower the time-average specific power, thereby increasing burnup.(author)

  2. The temperature behaviour of the elastic and thermodynamic properties of fcc thorium

    Energy Technology Data Exchange (ETDEWEB)

    Jaroszewicz, S., E-mail: jaroszew@tandar.cnea.gov.ar [Gerencia de Investigacion y Aplicaciones, Comision Nacional de Energia Atomica, Av. Gral. Paz 1499, San Martin (Argentina); Instituto de Tecnologia Jorge A. Sabato, UNSAM-CNEA (Argentina); Mosca, H.O. [Gerencia de Investigacion y Aplicaciones, Comision Nacional de Energia Atomica, Av. Gral. Paz 1499, San Martin (Argentina); Instituto de Tecnologia Jorge A. Sabato, UNSAM-CNEA (Argentina); Garces, J.E. [DAEE, Centro Atomico Bariloche, Comisin Nacional de Energia Atomica, Av. Bustillo 9500, Bariloche, Rio Negro (Argentina)

    2012-10-15

    The temperature behaviour of the structural, elastical and thermal properties of fcc thorium have been calculated from a free-parameter Helmholtz free energy developed by computing the cohesive energy from first principles calculations coupled to the Chen-Moebius lattice inversion method and the Debye-Grueneisen quasiharmonic model. The elastic constants, shear modulus, Young modulus, Poisson's ratio and thermodynamic properties of fcc Th as the entropy, the harmonic specific heat, the (P, V, T) equation of state and the thermal lattice expansion are found to be in a very good agreement with experiments and ab initio phonon calculations. The results of this work show the potentiality of the Chen-Moebius method coupled to ab initio calculation of the cohesive energy to develop a free-parameter pair potential capable of giving an overall description of fcc Th properties at T = 0 K with an error similar to ab initio calculations.

  3. Core loading pattern optimization of thorium fueled heavy water breeder reactor using genetic algorithm

    Energy Technology Data Exchange (ETDEWEB)

    Soewono, C. N.; Takaki, N. [Dept. of Applied Science Engineering, Faculty Tokai Univ., Kanagawa-ken, Hiratsuka-shi Kitakaname 4-1-1 (Japan)

    2012-07-01

    In this work genetic algorithm was proposed to solve fuel loading pattern optimization problem in thorium fueled heavy water reactor. The objective function of optimization was to maximize the conversion ratio and minimize power peaking factor. Those objectives were simultaneously optimized using non-dominated Pareto-based population ranking optimal method. Members of non-dominated population were assigned selection probabilities based on their rankings in a manner similar to Baker's single criterion ranking selection procedure. A selected non-dominated member was bred through simple mutation or one-point crossover process to produce a new member. The genetic algorithm program was developed in FORTRAN 90 while neutronic calculation and analysis was done by COREBN code, a module of core burn-up calculation for SRAC. (authors)

  4. Uranium: biokinetics and toxicity; Biocinetique et toxicite de l'uranium

    Energy Technology Data Exchange (ETDEWEB)

    Menetrier, F.; Renaud-Salis, V.; Flury-Herard, A

    2000-07-01

    This report was achieved as a part of a collaboration with the Fuel Cycle Direction. Its aim was to give the state of the art about: the behaviour of uranium in the human organism (biokinetics) after ingestion, its toxicity (mainly renal) and the current regulation about its incorporation. Both in the upstream and in the downstream of the fuel cycle, uranium remains, quantitatively, the first element in the cycle which is, at the present time, temporarily disposed or recycled. Such a considerable quantity of uranium sets the problem of its risk on the health. In the long term, the biosphere may be affected and consequently the public may ingest water or food contaminated with uranium. In this way, radiological and chemical toxicity risk may be activated. This report emphasizes: the necessity of confirming some experimental and epidemiological biokinetic data used or not in the ICRP models. Unsolved questions remain about the gastrointestinal absorption according to chemical form (valency state, mixtures...), mass and individual variations (age, disease) further a chronic ingestion of uranium. It is well established that uranium is mainly deposited in the skeleton and the kidney. But the skeleton kinetics following a chronic ingestion and especially in some diseases has to be more elucidated; the necessity of taking into account uranium at first as a chemical toxic, essentially in the kidney and determining the threshold of functional lesion. In this way, it is important to look for some specific markers; the problem of not considering chemical toxicity of uranium in the texts regulating its incorporation.

  5. High-temperature phase transitions, spectroscopic properties, and dimensionality reduction in rubidium thorium molybdate family.

    Science.gov (United States)

    Xiao, Bin; Gesing, Thorsten M; Kegler, Philip; Modolo, Giuseppe; Bosbach, Dirk; Schlenz, Hartmut; Suleimanov, Evgeny V; Alekseev, Evgeny V

    2014-03-17

    Four new rubidium thorium molybdates have been synthesized by high-temperature solid-state reactions. The crystal structures of Rb8Th(MoO4)6, Rb2Th(MoO4)3, Rb4Th(MoO4)4, and Rb4Th5(MoO4)12 were determined using single-crystal X-ray diffraction. All these compounds construct from MoO4 tetrahedra and ThO8 square antiprisms. The studied compounds adopt the whole range of possible structure dimensionalities from zero-dimensional (0D) to three-dimensional (3D): finite clusters, chains, sheets, and frameworks. Rb8Th(MoO4)6 crystallizes in 0D containing clusters of [Th(MoO4)6](8-). The crystal structure of Rb2Th(MoO4)3 is based upon one-dimensional chains with configuration units of [Th(MoO4)3](2-). Two-dimensional sheets occur in compound Rb4Th(MoO4)4, and a 3D framework with channels formed by thorium and molybdate polyhedra has been observed in Rb4Th5(MoO4)12. The Raman and IR spectroscopic properties of these compounds are reported. Temperature-depended phase transition effects were observed in Rb2Th(MoO4)3 and Rb4Th(MoO4)4 using thermogravimetry-differential scanning calorimetry analysis and high-temperature powder diffraction methods.

  6. Thorium isotopes tracing the iron cycle at the Hawaii Ocean Time-series Station ALOHA

    Science.gov (United States)

    Hayes, Christopher T.; Fitzsimmons, Jessica N.; Boyle, Edward A.; McGee, David; Anderson, Robert F.; Weisend, Rachel; Morton, Peter L.

    2015-11-01

    The role of iron as a limiting micronutrient motivates an effort to understand the supply and removal of lithogenic trace metals in the ocean. The long-lived thorium isotopes (232Th and 230Th) in seawater can be used to quantify the input of lithogenic metals attributable to the partial dissolution of aerosol dust. Thus, Th can help in disentangling the Fe cycle by providing an estimate of its ultimate supply and turnover rate. Here we present time-series (1994-2014) data on thorium isotopes and iron concentrations in seawater from the Hawaii Ocean Time-series Station ALOHA. By comparing Th-based dissolved Fe fluxes with measured dissolved Fe inventories, we derive Fe residence times of 6-12 months for the surface ocean. Therefore, Fe inventories in the surface ocean are sensitive to seasonal changes in dust input. Ultrafiltration results further reveal that Th has a much lower colloidal content than Fe does, despite a common source. On this basis, we suggest Fe colloids may be predominantly organic in composition, at least at Station ALOHA. In the deep ocean (>2 km), Fe approaches a solubility limit while Th, surprisingly, is continually leached from lithogenic particles. This distinction has implications for the relevance of Fe ligand availability in the deep ocean, but also suggests Th is not a good tracer for Fe in deep waters. While uncovering divergent behavior of these elements in the water column, this study finds that dissolved Th flux is a suitable proxy for the supply of Fe from dust in the remote surface ocean.

  7. The study of structure in 224–234 thorium nuclei within the framework IBM

    Directory of Open Access Journals (Sweden)

    Lee Su Youn

    2017-01-01

    Full Text Available An investigation has been made of the behaviour of nuclear structure as a function of an increase in neutron number from 224Th to 234Th. Thorium of mass number 234 is a typical rotor nucleus that can be explained by the SU(3 limit of the interacting boson model(IBM in the algebraic nuclear model. Furthermore, 224−232Th lie on the path of the symmetry-breaking phase transition. Moreover, the nuclear structure of 224Th can be explained using X(5 symmetry. However, as 226−230Th nuclei are not fully symmetrical nuclei, they can be represented by adding a perturbed term to express symmetry breaking. Through the following three calculation steps, we identified the tendency of change in nuclear structure. Firstly, the structure of 232Th is described using the matrix elements of the Hamiltonian and the electric quadrupole operator between basis states of the SU(3 limit in IBM. Secondly, the low-lying energy levels and E2 transition ratios corresponding to the observable physical values are calculated by adding a perturbed term with the first-order Casimir operator of the U(5 limit to the SU(3 Hamiltonian in IBM. We compared the results with experimental data of 224−234Th. Lastly, the potential of the Bohr Hamiltonian is represented by a harmonic oscillator, as a result of which the structure of 224−234Th could be expressed in closed form by an approximate separation of variables. The results of these theoretical predictions clarify nuclear structure changes in Thorium nuclei over mass numbers of practical significance.

  8. The study of structure in 224-234 thorium nuclei within the framework IBM

    Science.gov (United States)

    Lee, Su Youn; Lee, Young Jun; Lee, J. H.

    2017-09-01

    An investigation has been made of the behaviour of nuclear structure as a function of an increase in neutron number from 224Th to 234Th. Thorium of mass number 234 is a typical rotor nucleus that can be explained by the SU(3) limit of the interacting boson model(IBM) in the algebraic nuclear model. Furthermore, 224-232Th lie on the path of the symmetry-breaking phase transition. Moreover, the nuclear structure of 224Th can be explained using X(5) symmetry. However, as 226-230Th nuclei are not fully symmetrical nuclei, they can be represented by adding a perturbed term to express symmetry breaking. Through the following three calculation steps, we identified the tendency of change in nuclear structure. Firstly, the structure of 232Th is described using the matrix elements of the Hamiltonian and the electric quadrupole operator between basis states of the SU(3) limit in IBM. Secondly, the low-lying energy levels and E2 transition ratios corresponding to the observable physical values are calculated by adding a perturbed term with the first-order Casimir operator of the U(5) limit to the SU(3) Hamiltonian in IBM. We compared the results with experimental data of 224-234Th. Lastly, the potential of the Bohr Hamiltonian is represented by a harmonic oscillator, as a result of which the structure of 224-234Th could be expressed in closed form by an approximate separation of variables. The results of these theoretical predictions clarify nuclear structure changes in Thorium nuclei over mass numbers of practical significance.

  9. Uranium deposits of the world. Europe

    Energy Technology Data Exchange (ETDEWEB)

    Dahlkamp, Franz J.

    2016-07-01

    Uranium Deposits of the World, in three volumes, comprises an unprecedented compilation of data and descriptions of the uranium regions in Asia, USA, Latin America and Europe structured by countries. With this third, the Europe volume, Uranium Deposits of the World presents the most extensive data collection of the set. It covers about 140 uranium regions in more than 20 European countries with nearly 1000 mentioned uranium deposits. Each country and region receives an analytical overview followed by the geologically- and economically-relevant synopsis of the individual regions and fields. The presentations are structured in three major sections: (a) location and magnitude of uranium regions, districts, and deposits, (b) principal features of regions and districts, and (c) detailed characteristics of selected ore fields and deposits. This includes sections on geology, alteration, mineralization, shape and dimensions of deposits, isotopes data, ore control and recognition criteria, and metallogenesis. Beside the main European uranium regions, for example in the Czech Republic, Eastern Germany, France, the Iberian Peninsula or Ukraine, also small regions an districts to the point of singular occurrences of interest are considered. This by far the most comprehensive presentation of European uranium geology and mining would not be possible without the author's access to extensive information covering the countries of the former Eastern Bloc states, which was partly not previously available. Abundantly illustrated with information-laden maps and charts throughout, this reference work is an indispensable tool for geologists, mining companies, government agencies, and others with an interest in European key natural resources. A great help for the reader's orientation are the substantial bibliography of uranium-related publications and the indices, latter containing about 3900 entries in the geographical part alone. The three volumes of Uranium Deposits of the

  10. [Contact dermatitis from polyacrylate in TENS electrode].

    Science.gov (United States)

    Weber-Muller, F; Reichert-Penetrat, S; Schmutz, J-L; Barbaud, A

    2004-05-01

    Transcutaneous electric nerve stimulation (TENS) is useful for many chronic pains. It induces few serious side effects, but skin reactions are not rare. We report on two cases of contact dermatitis due to TENS electrodes by sensitization to the acrylate in TENS conductive gel. A 50 year-old man suffered from post-traumatic lumbar pair. He developed eczematous lesions on the sites where the TENS electrodes were applied. Patch tests were positive with the TENS gel, with ethylene glycol dimethylacrylate (2 p. 100 petrolatum) and ethyl-acrylate (2 p. 100 petrolatum) on day 2 and 4 readings. A 54 Year-old man had a paralysis of the foot elevator following rupture of an aneurysm. After 2 months, he had an eczema on the sites where the TENS electrodes were applied. Patch tests were negative with the TENS electrodes but positive with 2-hydroxyethyl acrylate (0.1 p. 100 petrolatum), triethyleneglycol diacrylate (0.1 p. 100 petrolatum), 2-hydroxyethyl methacrylate (2 p. 100 petrolatum) and 2-hydroxypropyl methacrylate (2 p. 100 petrolatum) on day 2 and 4 readings. TENS transmits small electrical currents through the skin that induce the depolarization of the affected sensory nerve endings. They have few serious side effects but skin reactions such as irritation, burns or allergy to propylene glycol in the electrode gel, to the rubber of the electrodes (mercaptobenzothiazole) or to the metallic part of the electrodes, i.e. nickel, are not uncommon. To our knowledge, only one case of an allergy to the polyacrylates of TENS electrode gel has been previously reported in the literature. We emphasize that acrylate could be the main sensitizer in the more recently commercialized TENS electrodes and will propose alternative ways of treating patients sensitized to acrylate and who require treatment with TENS.

  11. Study of reactions between uranium-plutonium mixed oxide and uranium nitride and between uranium oxide and uranium nitride; Etude des reactions entre l`oxyde mixte d`uranium-plutonium et le nitrure d`uranium et entre l`oxyde d`uranium et le nitrure d`uranium

    Energy Technology Data Exchange (ETDEWEB)

    Lecraz, C.

    1993-06-11

    A new type of combustible elements which is a mixture of uranium nitride and uranium-plutonium oxide could be used for Quick Neutrons Reactors. Three different studies have been made on the one hand on the reactions between uranium nitride (UN) and uranium-plutonium mixed oxide (U,Pu)O{sub 2}, on the other hand on these between UN and uranium oxide UO{sub 2}. They show a sizeable reaction between nitride and oxide for the studied temperatures range (1573 K to 1973 K). This reaction forms a oxynitride compound, MO{sub x} N{sub y} with M=U or M=(U,Pu), whose crystalline structure is similar to oxide`s. Solubility of nitride in both oxides is studied, as the reaction kinetics. (TEC). 32 refs., 48 figs., 22 tabs.

  12. ZDC Effective Cross Section for Uranium-Uranium Collisions in Run 12

    Energy Technology Data Exchange (ETDEWEB)

    Drees, A. [Brookhaven National Lab. (BNL), Upton, NY (United States)

    2013-12-09

    An accurate calibration of the luminosity measurement of the 2012 Uranium-Uranium RHIC run at 96 GeV per beam is of the greatest importance in order to measure the total uranium-uranium cross section with a reasonably small error bar. During the run, which lasted from April 20th to May 15th 2012, three vernier scans per experiment were performed. Beam intensities of up to 3.4 1010 Uranium ions in one ring were successfully accelerated to flattop at γ = 103.48 corresponding to 96 GeV/beam. The desired model β value was 0.7 m in the two low beta Interaction Points IP6 and IP8. With these beam parameters interaction rates of up to 15 kHz were achieved. This note presents the data associated with the vernier scans, and discusses the results and systematic effects.

  13. Electrochemical behaviour of thorium(IV) in molten LiF-CaF{sub 2} medium on inert and reactive electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Chamelot, P. [Universite de Toulouse, INPT, UPS, Laboratoire de Genie Chimique, Departement Procedes Electrochimiques, F-31062 Toulouse Cedex 09, France, CNRS, Laboratoire de Genie Chimique, F-31062 Toulouse Cedex 09 (France); Massot, L., E-mail: massot@chimie.ups-tlse.f [Universite de Toulouse, INPT, UPS, Laboratoire de Genie Chimique, Departement Procedes Electrochimiques, F-31062 Toulouse Cedex 09, France, CNRS, Laboratoire de Genie Chimique, F-31062 Toulouse Cedex 09 (France); Cassayre, L.; Taxil, P. [Universite de Toulouse, INPT, UPS, Laboratoire de Genie Chimique, Departement Procedes Electrochimiques, F-31062 Toulouse Cedex 09, France, CNRS, Laboratoire de Genie Chimique, F-31062 Toulouse Cedex 09 (France)

    2010-06-30

    The electrochemical behaviour of the Th(IV)/Th system was examined in molten LiF-CaF{sub 2} medium on inert (molybdenum), reactive (nickel) and liquid (bismuth) electrodes in the 810-920 deg. C temperature range by several electrochemical techniques. Experimental results showed that (i) thorium fluoride was reduced in a single step exchanging 4 electrons and limited by thorium ions diffusion in the solution, (ii) the oxide ions induce the precipitation of Th(IV) in the form of thorium oxide (ThO{sub 2}), in a process involving as intermediate compound a soluble oxifluoride (ThOF{sub 2}), (iii) the reduction of thorium ions on reactive (Ni and liquid Bi) electrodes yields compounds Ni-Th and Bi-Th with a potential shift of around 0.7 V (for Ni and Bi) more anodic than the reduction of Th(IV) on inert substrate.

  14. Investigation of uranium (VI) adsorption by polypyrrole

    Energy Technology Data Exchange (ETDEWEB)

    Abdi, S. [Faculty of Chemical, Petroleum and Gas Engineering, Semnan University, Semnan 35195-363 (Iran, Islamic Republic of); Nasiri, M., E-mail: mnasiri@semnan.ac.ir [Faculty of Chemical, Petroleum and Gas Engineering, Semnan University, Semnan 35195-363 (Iran, Islamic Republic of); Mesbahi, A. [Faculty of Chemical, Petroleum and Gas Engineering, Semnan University, Semnan 35195-363 (Iran, Islamic Republic of); Khani, M.H. [Nuclear Fuel Cycle Research School, Nuclear Science and Technology Research Institute, Tehran, 14395-836 (Iran, Islamic Republic of)

    2017-06-15

    Highlights: • The adsorbent (polypyrrole) was synthesized by a chemical method using PEG, DBSNa and CTAB as the surfactant. • The solution pH was one of the most important parameters affecting the adsorption of uranium. • The CTAB provided higher removal percentage compared with the other surfactants. • The maximum adsorption capacity obtained from Langmuir isotherm was 87.72 mg/g. • The pseudo second-order model fitted well with the adsorption kinetic of polypyrrole to uranium. - Abstract: The purpose of this study was to investigate the adsorption of uranium (VI) ions on the polypyrrole adsorbent. Polypyrrole was synthesized by a chemical method using polyethylene glycol, sodium dodecylbenzenesulfonate, and cetyltrimethylammonium bromide as the surfactant and iron (III) chloride as an oxidant in the aqueous solution. The effect of various surfactants on the synthesized polymers and their performance as the uranium adsorbent were investigated. Adsorbent properties were characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) techniques. The effect of different parameters such as pH, contact time, initial metal ion concentrations, adsorbent dose, and the temperature was investigated in the batch system for uranium adsorption process. It has been illustrated that the adsorption equilibrium time is 7 min. The results showed that the Freundlich model had the best agreement and the maximum adsorption capacity of polypyrrole for uranium (VI) was determined 87.72 mg/g from Langmuir isotherm. In addition, the mentioned adsorption process was fast and the kinetic data were fitted to the Pseudo first and second order models. The adsorption kinetic data followed the pseudo-second-order kinetic model. Moreover, the thermodynamic parameters ΔG{sup 0}, ΔH{sup 0} and ΔS{sup 0} showed that the uranium adsorption process by polypyrrole was endothermic and spontaneous.

  15. Clinical experience with TENS and TENS combined with nitrous oxide-oxygen. Report of 371 patients.

    OpenAIRE

    Quarnstrom, F. C.; Milgrom, P.

    1989-01-01

    Transcutaneous electrical nerve stimulation (TENS) alone or TENS combined with nitrous oxide-oxygen (N2O) was administered for restorative dentistry without local anesthesia to 371 adult patients. A total of 55% of TENS alone and 84% of TENS/N2O visits were rated successful. A total of 53% of TENS alone and 82% of TENS/N2O patients reported slight or no pain. In multivariable analyses, pain reports were related to the anesthesia technique and patient fear and unrelated to sex, race, age, toot...

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

    Energy Technology Data Exchange (ETDEWEB)

    Barlow, C.R.; Alderson, J.H.; Blue, S.C.; Boelens, R.A.; Conkel, M.E.; Dorning, R.E.; Ecklund, C.D.; Halicks, W.G.; Henson, H.M.; Newman, V.S.; Philpot, H.E.; Taylor, M.S.; Vournazos, J.P. [Oak Ridge K-25 Site, TN (United States). UEO Enrichment Technical Operations Div.; Russell, J.R. [USDOE Oak Ridge Field Office, TN (United States); Pryor, W.A. [PAI Corp., Oak Ridge, TN