Uranium 2000 : International symposium on the process metallurgy of uranium

International Nuclear Information System (INIS)

Ozberk, E.; Oliver, A.J.

2000-01-01

The International Symposium on the Process Metallurgy of Uranium has been organized as the thirtieth annual meeting of the Hydrometallurgy Section of the Metallurgical Society of the Canadian Institute of Mining, Metallurgy and Petroleum (CIM). This meeting is jointly organized with the Canadian Mineral Processors Division of CIM. The proceedings are a collection of papers from fifteen countries covering the latest research, development, industrial practices and regulatory issues in uranium processing, providing a concise description of the state of this industry. Topics include: uranium industry overview; current milling operations; in-situ uranium mines and processing plants; uranium recovery and further processing; uranium leaching; uranium operations effluent water treatment; tailings disposal, water treatment and decommissioning; mine decommissioning; and international regulations and decommissioning. (author)

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

International Nuclear Information System (INIS)

Silva, T.M. da.

1988-01-01

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

Laboratory simulation studies of uranium mobility in natural waters

International Nuclear Information System (INIS)

Giblin, A.M.; Swaine, D.J.; Batts, B.D.

1981-01-01

The effects of imposed variations of pH and Eh on aqueous uranium mobility at 25 0 C have been studied in three simulations of natural water systems. Constituents tested for their effect on uranium mobility were: (a) hydrous ferric oxide, to represent adsorptive solids which precipitate or dissolve in response to variations in pH and Eh; (b) kaolinite, representing minerals which, although modified by pH and Eh changes, are present as solids over the pH-Eh range of natural waters; and (c) carbonate, to represent a strong uranium-complexing species. Uranium mobility measurements from each simulation were regressed against pH and Eh within a range appropriate to natural waters. Hydrous ferric oxide and kaolinite each affected uranium mobility, but in separate pH-Eh domains. Aqueous carbonate increased mobility of uranium, and adsorption of UO 2 (CO 3 ) 3 4- caused colloidal dispersion of hydrous ferric oxide, possibly explaining the presence of 'hydrothermal hematite' in some uranium deposits. Enhanced uranium mobility observed in the pH-Eh domains of thermodynamically insoluble uranium oxides could be explained if the oxides were present as colloids. Uranium persisting as a mobile species, even after reduction, has implications for the near surface genesis of uranium ores. (author)

PROCESS OF RECOVERING URANIUM

Science.gov (United States)

Carter, J.M.; Larson, C.E.

1958-10-01

A process is presented for recovering uranium values from calutron deposits. The process consists in treating such deposits to produce an oxidlzed acidic solution containing uranium together with the following imparities: Cu, Fe, Cr, Ni, Mn, Zn. The uranium is recovered from such an impurity-bearing solution by adjusting the pH of the solution to the range 1.5 to 3.0 and then treating the solution with hydrogen peroxide. This results in the precipitation of uranium peroxide which is substantially free of the metal impurities in the solution. The peroxide precipitate is then separated from the solution, washed, and calcined to produce uranium trioxide.

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

International Nuclear Information System (INIS)

Silva Neto, Joao Batista da

2008-01-01

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

The market for natural uranium

International Nuclear Information System (INIS)

Bauder, P.

1981-01-01

The natural uranium market is characterized at present by its surplus. This is essentially due to a surplus on the production line. The uranium produced is no longer taken up by the market as it was up to the middle of 1979. The object of this contribution is therefore a survey on the present availability and demand situation, as well as to discuss market mechanisms and forecast the future market trend. (orig./IHO) [de

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

International Nuclear Information System (INIS)

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

2017-01-01

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

Aspects on optimization of natural uranium fuel utilization in heavy water reactors

International Nuclear Information System (INIS)

1978-08-01

This paper is dealing with a possibility to decrease the natural uranium consumption of CANDU PHWR using the once-through cycle. This possibility is based on the utilization of slightly enriched uranium. The optimal two-zone structure of a reactor using natural uranium is found out. The optimal criterium is the maximization of the burnup (equivalent to minimization of uranium requirements) with a constraint on power density radial uniformity factor. As regards the enriched uranium, the optimal enrichment and the two-zone structure of a reactor which minimizes the natural uranium requirement with constraints on uniformity factor and maximum burnup are established. Corresponding to a maximum burnup of 16,000 MWd/t and 1% enrichment, the natural uranium requirement is found to be 10% less than that of the natural uranium reactor

Study on removal effect and mechanism of uranium by hydroxyapatite and natural apatite

International Nuclear Information System (INIS)

Zhang Xiaofeng; Chen Diyun; Tu Guoqing; Huang Xiaozhui

2014-01-01

By the static experiments, the effects of reaction time, pH value, initial concentration of uranium, dosage of apatite on adsorption of hydroxyapatite and natural apatite for uranium were studied respectively. The adsorption process was analyzed by thermodynamics and kinetics, and the adsorption mechanism was analyzed by infrared spectroscopy, X-ray diffraction and scanning electron microscope. The results of hydroxyapatite show that the removal capacity of uranium increases with the initial concentration of uranium, and the adsorption rate of hydroxyapatite on UO_2"2"+ reaches 85%, when the pH value is 4 to 5 and dosage of hydroxyapatite is 0.75 g. The results of natural apatite show that the removal capacity of uranium increases with the initial concentration of uranium, and the adsorption rate of natural apatite on UO_2"2"+ is up to 80%, when the pH value is 3 and dosage of hydroxyapatite is l.0 g. Similarly, at 120 minutes both of the removal reactions by hydroxyapatite and natural apatite substantially reach equilibrium. Moreover, both of the reactions by hydroxyapatite and natural apatite are in line with quasi secondary dynamics equation, and follow the Langmuir adsorption isotherm. Infrared spectra indicate that the removal of hydroxyapatite for uranium depends on the complexation of phosphate, which is almost the same as that of natural apatite. X-ray diffraction analysis shows that hydroxyapatite has the composition and structure of pure material, whereas the natural apatite is mainly composed of Ca_5H_2(PO_4)_3F and Ca_8H_2(PO_4)_6H_2O. In addition, scanning electron microscope demonstrates that hydroxyapatite has the appearance of spherical with a hole and the hole has a cavity containing a large amount of floc, while the surface becomes smooth and pores are closed after removal of uranium, which is due to the adsorption of UO_2"2"+ leading a link between molecules on hydroxyapatite surface. But for natural apatite, it depicts the angular mineral shape

Uranium Biomineralization By Natural Microbial Phosphatase Activities in the Subsurface

Energy Technology Data Exchange (ETDEWEB)

Taillefert, Martial [Georgia Tech Research Corporation, Atlanta, GA (United States)

2015-04-01

This project investigated the geochemical and microbial processes associated with the biomineralization of radionuclides in subsurface soils. During this study, it was determined that microbial communities from the Oak Ridge Field Research subsurface are able to express phosphatase activities that hydrolyze exogenous organophosphate compounds and result in the non-reductive bioimmobilization of U(VI) phosphate minerals in both aerobic and anaerobic conditions. The changes of the microbial community structure associated with the biomineralization of U(VI) was determined to identify the main organisms involved in the biomineralization process, and the complete genome of two isolates was sequenced. In addition, it was determined that both phytate, the main source of natural organophosphate compounds in natural environments, and polyphosphate accumulated in cells could also be hydrolyzed by native microbial population to liberate enough orthophosphate and precipitate uranium phosphate minerals. Finally, the minerals produced during this process are stable in low pH conditions or environments where the production of dissolved inorganic carbon is moderate. These findings suggest that the biomineralization of U(VI) phosphate minerals is an attractive bioremediation strategy to uranium bioreduction in low pH uranium-contaminated environments. These efforts support the goals of the SBR long-term performance measure by providing key information on "biological processes influencing the form and mobility of DOE contaminants in the subsurface".

Radioactive wastes of uranium mining and milling: Radiological consequences for human population and natural environment

International Nuclear Information System (INIS)

Sazykina, T.G.; Kryshev, I.I.

2002-01-01

The sources of wastes and levels of radioactive contamination are considered in the areas of uranium ore mining and milling. Assessments of doses to the population are made using the methodology of multiple sources and pathways of exposure, including calculations of inhalation dose and doses from consumption of contaminated agricultural and natural products, as well as external exposure from the radioactive cloud and soil. On the local (0-100 km) spatial scale, the dose from uranium mining and processing is, on average, about 0.7 man Sv (GWa) -1 . The most significant pathway of the population exposure is inhalation of radon. The impact of uranium ore mining and processing on natural flora and fauna is determined by specific characteristics of the production at uranium mining enterprises and has both radiation and non-radiation components. The estimates of external and internal exposures to the natural biota in the vicinity of hydro-metallurgical works and tailing dumps are presented. (author)

Immobilization of uranium in contaminated soil by natural apatite addition

International Nuclear Information System (INIS)

Mrdakovic Popic, Jelena; Stojanovic, Mirjana; Milosevic, Sinisa; Iles, Deana; Zildzovic, Snezana

2007-01-01

Available in abstract form only. Full text of publication follows: The goal of this study was to evaluate the effectiveness of Serbian natural mineral apatite as soil additive for reducing the migration of uranium from contaminated sediments. In laboratory study we investigated the sorption properties of domestic apatite upon different experimental conditions, such as pH, adsorbent mass, reaction period, concentration of P 2 O 5 in apatite, solid/liquid ratio. In second part of study, we did the quantification of uranium in soil samples, taken from uranium mine site 'Kalna', by sequential extraction method. The same procedure was, also, used for uranium determination in contaminated soil samples after apatite addition, in order to determine the changes in U distribution in soil fraction. The obtained results showed the significant level of immobilization (96.7%) upon certain conditions. Increase of %P 2 O 5 in apatite and process of mechano-chemical activation led to increase of immobilization capacity from 17.50% till 91.64%. The best results for uranium binding were obtained at pH 5.5 and reaction period 60 days (98.04%) The sequential extraction showed the presence of uranium (48.2%) in potentially available soil fractions, but with the apatite addition uranium content in these fractions decreased (30.64%), what is considering environmental aspect significant fact. In situ immobilization of radionuclide using inexpensive sequestering agents, such as apatite, is very adequate for big contaminated areas of soil with low level of contamination. This investigation study on natural apatite from deposit 'Lisina' Serbia was the first one of this type in our country. Key words: apatite, uranium, immobilization, soil, contamination. (authors)

Natural analogue study of uranium deposits in Japan with special reference to the Tono uranium deposit

International Nuclear Information System (INIS)

Komuro, Kosei; Sasao, Eiji

2004-05-01

In order to verify the safety assessment for geological disposal system of high-level radioactive waste, it is necessary to evaluate properly the stability of the disposal system under natural hydrogeological environment over long period of time (ten to hundred thousands years). For the safety assessment for that in the Japanese Islands, many geological processes inherent in the tectonically active Island-Arc system should be also taken into consideration in addition to those in stable continental environment. However, it is difficult because some processes such as earthquake seem to be accidental and some are periodic or gradual over our life scale. The uranium deposits in Japan are subjected to many geological processes inherent in the tectonically active Island-Arc system. The studies on long-term preservation of uranium deposits in Japan from a natural analogue viewpoint would be expected to provide useful information for the assessment in the Japanese Islands over long period of time. In order to understand the behavior of radionuclides under natural hydrogeological environment in Japanese Islands over long period of time, the uranium deposits in Japan, especially of the Tono uranium deposit was investigated from a natural analogue viewpoint under the course of joint research program by University of Tsukuba and Japan Nuclear Cycle Development Institute. Important conclusions obtained in the present study are summarized as follows: The migration behavior of the radionuclides in the granite area is mainly controlled by the stability of original minerals in oxic condition, being due to poor reducing agents such as organic matter and sulfide minerals. In the case of hydrothermal alteration, yttrialite and fergusonite were decomposed and thorogummite was formed at the altered part, whereas zircon and allanite have not been significantly altered. In the case of weathering, autunite and torbernite were formed, probably due to the high phosphorus weathering

Paleo-channel deposition of natural uranium at a US Air Force landfill

International Nuclear Information System (INIS)

Young, Carl; Weismann, Joseph; Caputo, Daniel

2007-01-01

Available in abstract form only. Full text of publication follows: The US Air Force sought to identify the source of radionuclides that were detected in groundwater surrounding a closed solid waste landfill at the former Lowry Air Force Base in Denver, Colorado, USA. Gross alpha, gross beta, and uranium levels in groundwater were thought to exceed US drinking water standards and down-gradient concentrations exceeded up-gradient concentrations. Our study has concluded that the elevated radionuclide concentrations are due to naturally-occurring uranium in the regional watershed and that the uranium is being released from paleo-channel sediments beneath the site. Groundwater samples were collected from monitor wells, surface water and sediments over four consecutive quarters. A list of 23 radionuclides was developed for analysis based on historical landfill records. Concentrations of major ions and metals and standard geochemical parameters were analyzed. The only radionuclide found to be above regulatory standards was uranium. A search of regional records shows that uranium is abundant in the upstream drainage basin. Analysis of uranium isotopic ratios shows that the uranium has not been processed for enrichment nor is it depleted uranium. There is however slight enrichment in the U-234:U- 238 activity ratio, which is consistent with uranium that has undergone aqueous transport. Comparison of up-gradient versus down-gradient uranium concentrations in groundwater confirms that higher uranium concentrations are found in the down-gradient wells. The US drinking water standard of 30 μg/L for uranium was exceeded in some of the up-gradient wells and in most of the down-gradient wells. Several lines of evidence indicate that natural uranium occurring in streams has been preferentially deposited in paleo-channel sediments beneath the site, and that the paleo-channel deposits are causing the increased uranium concentrations in down-gradient groundwater compared to up

Sorption of natural uranium by algerian bentonite

International Nuclear Information System (INIS)

Megouda, N.; Kadi, H.; Hamla, M.S.; Brahimi, H.

2004-01-01

Full text.Batch sorption experiments have been used to assess the sorption behaviour of uranium onto natural and drilling bentonites. The operating parameters (pH, aolis-liquid ratio, particle size, time and initial uranium concentration) influenced the rate of adsorption. The distribution coefficient (Kd) range values at equilibrium time are 45.95-1079.26 ml/g and 32.81-463053 ml/g for the drilling and natural bentonites respectively. The equilibrium isotherms show that the data correlate with both Freundlich and Langmuir models

Innovative Elution Processes for Recovering Uranium from Seawater

International Nuclear Information System (INIS)

Wai, Chien; Tian, Guoxin; Janke, Christopher

2014-01-01

Utilizing amidoxime-based polymer sorbents for extraction of uranium from seawater has attracted considerable interest in recent years. Uranium collected in the sorbent is recovered typically by elution with an acid. One drawback of acid elution is deterioration of the sorbent which is a significant factor that limits the economic competitiveness of the amidoxime-based sorbent systems for sequestering uranium from seawater. Developing innovative elution processes to improve efficiency and to minimize loss of sorbent capacity become essential in order to make this technology economically feasible for large-scale industrial applications. This project has evaluated several elution processes including acid elution, carbonate elution, and supercritical fluid elution for recovering uranium from amidoxime-based polymer sorbents. The elution efficiency, durability and sorbent regeneration for repeated uranium adsorption- desorption cycles in simulated seawater have been studied. Spectroscopic techniques are used to evaluate chemical nature of the sorbent before and after elution. A sodium carbonate-hydrogen peroxide elution process for effective removal of uranium from amidoxime-based sorbent is developed. The cause of this sodium carbonate and hydrogen peroxide synergistic leaching of uranium from amidoxime-based sorbent is attributed to the formation of an extremely stable uranyl peroxo-carbonato complex. The efficiency of uranium elution by the carbonate-hydrogen peroxide method is comparable to that of the hydrochloric acid elution but damage to the sorbent material is much less for the former. The carbonate- hydrogen peroxide elution also does not need any elaborate step to regenerate the sorbent as those required for hydrochloric acid leaching. Several CO2-soluble ligands have been tested for extraction of uranium from the sorbent in supercritical fluid carbon dioxide. A mixture of hexafluoroacetylacetone and tri-n-butylphosphate shows the best result but uranium

Innovative Elution Processes for Recovering Uranium from Seawater

Energy Technology Data Exchange (ETDEWEB)

Wai, Chien [Univ. of Idaho, Moscow, ID (United States); Tian, Guoxin [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Janke, Christopher [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

2014-05-29

Utilizing amidoxime-based polymer sorbents for extraction of uranium from seawater has attracted considerable interest in recent years. Uranium collected in the sorbent is recovered typically by elution with an acid. One drawback of acid elution is deterioration of the sorbent which is a significant factor that limits the economic competitiveness of the amidoxime-based sorbent systems for sequestering uranium from seawater. Developing innovative elution processes to improve efficiency and to minimize loss of sorbent capacity become essential in order to make this technology economically feasible for large-scale industrial applications. This project has evaluated several elution processes including acid elution, carbonate elution, and supercritical fluid elution for recovering uranium from amidoxime-based polymer sorbents. The elution efficiency, durability and sorbent regeneration for repeated uranium adsorption- desorption cycles in simulated seawater have been studied. Spectroscopic techniques are used to evaluate chemical nature of the sorbent before and after elution. A sodium carbonate-hydrogen peroxide elution process for effective removal of uranium from amidoxime-based sorbent is developed. The cause of this sodium carbonate and hydrogen peroxide synergistic leaching of uranium from amidoxime-based sorbent is attributed to the formation of an extremely stable uranyl peroxo-carbonato complex. The efficiency of uranium elution by the carbonate-hydrogen peroxide method is comparable to that of the hydrochloric acid elution but damage to the sorbent material is much less for the former. The carbonate- hydrogen peroxide elution also does not need any elaborate step to regenerate the sorbent as those required for hydrochloric acid leaching. Several CO2-soluble ligands have been tested for extraction of uranium from the sorbent in supercritical fluid carbon dioxide. A mixture of hexafluoroacetylacetone and tri-n-butylphosphate shows the best result but uranium

Mining and processing of uranium ores in the USSR

International Nuclear Information System (INIS)

Laskorin, B.N.; Mamilov, V.A.; Korejsho, Yu.A.

1983-01-01

Experience gained in uranium ore mining by modern methods in combination with underground and heap leaching is summarized. More intensive processing of low-grade ores has been achieved through the use of autoclave leaching, sorptive treatment of thick pulps, extractive separation of pure uranium compounds, automated continuous sorption devices of high efficiency for processing the underground- and heap-leaching liquors, natural and mine water, and recovery of molybdenum, vanadium, scandium, rare earths and phosphate fertilizers from low-grade ores. Production of ion-exchangers and extractants has been developed and processes for concomitant recovery of copper, gold, ionium, tungsten, caesium, zirconium, tantalum, nickel and cobalt have been designed. (author)

URANIUM LEACHING AND RECOVERY PROCESS

Science.gov (United States)

McClaine, L.A.

1959-08-18

A process is described for recovering uranium from carbonate leach solutions by precipitating uranium as a mixed oxidation state compound. Uranium is recovered by adding a quadrivalent uranium carbon;te solution to the carbonate solution, adjusting the pH to 13 or greater, and precipitating the uranium as a filterable mixed oxidation state compound. In the event vanadium occurs with the uranium, the vanadium is unaffected by the uranium precipitation step and remains in the carbonate solution. The uranium-free solution is electrolyzed in the cathode compartment of a mercury cathode diaphragm cell to reduce and precipitate the vanadium.

The light water natural uranium reactor

International Nuclear Information System (INIS)

Radkowsky, A.

A new type of light water seed blanket with the seed having 20% enrichment and the blanket a special combination of elements of natural uranium and thorium, relatively close packed, but sufficient spacing for heat transfer purpose is described. The blanket would deliver approximately half the total energy for about 10,000 MWDIT, so this type of core would be just as economical or better in uranium ore consumation as present cores. (author)

Uranium mobility in the natural environment - evidence from sedimentary roll-front deposits

International Nuclear Information System (INIS)

Deutsch, W.J.; Serne, R.J.

1983-04-01

Roll-front deposits consist of naturally occurring ore-grade uranium in selected sandstone aquifers throughout the world. The geochemical environment of these roll-front deposits is analogous to the environment of a radioactive waste repository containing redox-sensitive elements during its post-thermal period. The ore deposits are formed by a combination of dissolution, complexation, sorption/precipitation, and mineral formation processes. The uranium, leached from the soil by percolating rainwater, complexes with dissolved carbonate and moves in the oxidizing ground water at very low concentration (parts per billion) levels. The uranium is extracted from the leaching solution by the chemical processes, over long periods of time, at the interfaces between oxidized and reduced sediments. The Eh of the ground water associated with the reduced sediments (Eh = -100 mv to +100 mv) is higher than the Eh expected for most waste repository environments (Eh = -100 mv to -300 mv); this suggests that uranium solids will not be very soluble in the repositories. Data from in-situ leach mining and restoration of roll-front uranium deposits also provide information on the potential mobility of the waste if oxidizing ground water should enter the repository. Uranium solids probably will be initially very soluble in carbonate ground water; however, as reducing conditions are re-estblished through water/rock interactions, the uranium will reprecipitate and the amount of uranium in solution will again equilibrate with the reduced uranium minerals

Process for electrolytically preparing uranium metal

Science.gov (United States)

Haas, Paul A.

1989-01-01

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

Determination of 226Ra and natural uranium concentration in Botafogo river

International Nuclear Information System (INIS)

Nascimento, M.B. do; Amaral, R.S.; Khoury, H.J.; Andrade Lima, R. de

1990-01-01

In the Brazilian Northeast region at the coastal area from Pernambuco to Paraiba there is a 4 km wide strip deposit of phosphate rock. This phosphate is used to produce fertilizes by a factory located at the border of the Botafogo river, which cross this area. The phosphate is associated with uranium and no research has been conducted on the river radioactive contamination due the natural processes and to the fertizer factory the present investigation was undertaken to determine 226 Ra and natural uranium concentration in the river water, near the factory. Results show that the radionuclide concentration increases sharply in front of the place of the factory discharge and then decreases rapidly to the same levels found before the factory, 0,01 Bq/1. (author) [pt

Long-term outlook for global natural uranium and uranium enrichment supply and demand situations after the impact of Fukushima Daiichi Nuclear Power Plant accident

International Nuclear Information System (INIS)

Matsuo, Yuhji; Murakami, Tomoko

2012-01-01

In this paper, the authors propose long-term projections of global nuclear power generation, uranium production, and uranium enrichment capacities by region, and estimate the trade flows of natural uranium and uranium enrichment activities in 2020 and 2035. In spite of the rapid nuclear power generation capacity growth expected especially in Asia, the natural uranium and uranium enrichment trade will not be tightened by 2020 due to the projected increase in both natural uranium production and uranium enrichment capacities, which may cause a drop in natural uranium and uranium enrichment prices. Thus, there is a great possibility that the current projects for capacity expansion will be delayed considerably. However, in the 'high-demand scenario', where nuclear expansion will be accelerated due to growing concerns about global warming and energy security issues, additional investments in uranium production and enrichment facilities will be needed by 2035. In Asia, the self-sufficiency ratio for both natural uranium supply and uranium enrichment activities will remain relatively low until 2035. However, the Herfindahl-Hirschman (HH) index of natural uranium and uranium enrichment activity trade to Asia will be lowered considerably up to 2035, indicating that nuclear capacity expansion can contribute to enhancing energy security in Asia. (author)

Elimination of natural uranium and 226Ra from contaminated waters by rhizofiltration using Helianthus annuus L

International Nuclear Information System (INIS)

Vera Tome, F.; Blanco Rodriguez, P.; Lozano, J.C.

2008-01-01

The elimination of natural uranium and 226 Ra from contaminated waters by rhizofiltration was tested using Helianthus annuus L. (sunflower) seedlings growing in a hydroponic medium. Different experiments were designed to determine the optimum age of the seedlings for the remediation process, and also to study the principal way in which the radionuclides are removed from the solution by the sunflower roots. In every trial a precipitate appeared which contained a major fraction of the natural uranium and 226 Ra. The results indicated that the seedlings themselves induced the formation of this precipitate. When four-week-old seedlings were exposed to contaminated water, a period of only 2 days was sufficient to remove the natural uranium and 226 Ra from the solution: about 50% of the natural uranium and 70% of the 226 Ra were fixed in the roots, and essentially the rest was found in the precipitate, with only very small percentages fixed in the shoots and left in solution

Fluorometric analysis for uranium in natural waters

International Nuclear Information System (INIS)

Waterbury, G.R.

1977-01-01

A fluorometric method is used for the routine determination of uranium at 0.2 to parts-per-billion (ppB) concentrations in natural surface waters. Duplicate 200-μl aliquots of the water samples are pipetted onto 0.4-g pellets of 98 percent NaF-2 percent LiF flux contained in platinum dishes. The pellets are dried under heat lamps and fused over special propane burners. The fused pellets are subjected to ultraviolet radiation and the fluorescence is measured in a fluorometer. The lower limit of detection is 0.2 ppB of uranium, and the precision is about 15 relative percent in the 0.2 to 10 ppB uranium concentration range. Two analysts determine uranium in 750 to 900 samples per week using this method. Samples containing solids or more than 19 ppB of uranium are analyzed by a delayed neutron counting method

Uranium ore deposits: geology and processing implications

International Nuclear Information System (INIS)

Belyk, C.L.

2010-01-01

There are fifteen accepted types of uranium ore deposits and at least forty subtypes readily identified around the world. Each deposit type has a unique set of geological characteristics which may also result in unique processing implications. Primary uranium production in the past decade has predominantly come from only a few of these deposit types including: unconformity, sandstone, calcrete, intrusive, breccia complex and volcanic ones. Processing implications can vary widely between and within the different geological models. Some key characteristics of uranium deposits that may have processing implications include: ore grade, uranium and gangue mineralogy, ore hardness, porosity, uranium mineral morphology and carbon content. Processing difficulties may occur as a result of one or more of these characteristics. In order to meet future uranium demand, it is imperative that innovative processing approaches and new technological advances be developed in order that many of the marginally economic traditional and uneconomic non-traditional uranium ore deposits can be exploited. (author)

The separation of uranium ions by natural and modified diatomite from aqueous solution

Energy Technology Data Exchange (ETDEWEB)

Sprynskyy, Myroslav, E-mail: sprynsky@yahoo.com [Department of Environmental Chemistry and Bioanalytics, Faculty of Chemistry, Nicolaus Copernicus University, 7 Gagarina Str., 87-100 Torun (Poland); Kovalchuk, Iryna [Department of Environmental Chemistry and Bioanalytics, Faculty of Chemistry, Nicolaus Copernicus University, 7 Gagarina Str., 87-100 Torun (Poland); Institute of Adsorption and Problem of Endoecology, National Academy of Sciences of Ukraine, 13 General Naumov Str., 03164 Kyiv (Ukraine); Buszewski, Boguslaw [Department of Environmental Chemistry and Bioanalytics, Faculty of Chemistry, Nicolaus Copernicus University, 7 Gagarina Str., 87-100 Torun (Poland)

2010-09-15

In this work the natural and the surfactant modified diatomite has been tested for ability to remove uranium ions from aqueous solutions. Such controlling factors of the adsorption process as initial uranium concentration, pH, contact time and ionic strength have been investigated. Effect of ionic strength of solution has been examined using the solutions of NaCl, Na{sub 2}CO{sub 3} and K{sub 2}SO{sub 4}. The pseudo-first order and the pseudo-second order models have been used to analyze the adsorption kinetic results, whereas the Langmuir and the Freundlich isotherms have been used to the equilibrium adsorption data. The effects of the adsorbent modification as well as uranium adsorption on the diatomite surface have been studied using X-ray powder diffraction, scanning electron microscopy and FTIR spectroscopy. The maximum adsorption capacities of the natural and the modified diatomite towards uranium were 25.63 {mu}mol/g and 667.40 {mu}mol/g, respectively. The desorptive solutions of HCl, NaOH, Na{sub 2}CO{sub 3}, K{sub 2}SO{sub 4}, CaCO{sub 3}, humic acid, cool and hot water have been tested to recover uranium from the adsorbent. The highest values of uranium desorption (86%) have been reached using 0.1 M HCl.

The separation of uranium ions by natural and modified diatomite from aqueous solution.

Science.gov (United States)

Sprynskyy, Myroslav; Kovalchuk, Iryna; Buszewski, Bogusław

2010-09-15

In this work the natural and the surfactant modified diatomite has been tested for ability to remove uranium ions from aqueous solutions. Such controlling factors of the adsorption process as initial uranium concentration, pH, contact time and ionic strength have been investigated. Effect of ionic strength of solution has been examined using the solutions of NaCl, Na(2)CO(3) and K(2)SO(4). The pseudo-first order and the pseudo-second order models have been used to analyze the adsorption kinetic results, whereas the Langmuir and the Freundlich isotherms have been used to the equilibrium adsorption data. The effects of the adsorbent modification as well as uranium adsorption on the diatomite surface have been studied using X-ray powder diffraction, scanning electron microscopy and FTIR spectroscopy. The maximum adsorption capacities of the natural and the modified diatomite towards uranium were 25.63 micromol/g and 667.40 micromol/g, respectively. The desorptive solutions of HCl, NaOH, Na(2)CO(3), K(2)SO(4), CaCO(3), humic acid, cool and hot water have been tested to recover uranium from the adsorbent. The highest values of uranium desorption (86%) have been reached using 0.1M HCl. Copyright 2010 Elsevier B.V. All rights reserved.

Idaho National Engineering Laboratory materials in inventory natural and enriched uranium management and storage costs

International Nuclear Information System (INIS)

Nebeker, R.L.

1995-11-01

On July 13, 1994, the Office of Environmental Management (EM) was requested to develop a planning process that would result in management policies for dealing with nuclear materials in inventory. In response to this request, EM launched the Materials In Inventory (MIN) Initiative. A Headquarters Working Group was established to develop the broad policy framework for developing MIN management policies. MIN activities cover essentially all nuclear materials within the DOE complex, including such items as spent nuclear fuel, depleted uranium, plutonium, natural and enriched uranium, and other materials. In August 1995, a report discussing the natural and enriched uranium portion of the Initiative for the Idaho National Engineering Laboratory (INEL) was published. That report, 'Idaho National Engineering Laboratory Materials-in-Inventory, Natural and Enriched Uranium'.' identified MIN under the control of Lockheed Idaho Technologies Company at the INEL. Later, additional information related to the costs associated with the storage of MIN materials was requested to supplement this report. This report provides the cost information for storing, disposing, or consolidating the natural and enriched uranium portion of the MIN materials at the INEL. The information consists of eight specific tables which detail present management costs and estimated costs of future activities

Uranium

International Nuclear Information System (INIS)

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

1992-01-01

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

Long term developments in irradiated natural uranium processing costs. Optimal size and siting of plants; Perspectives a long terme des couts de traitement de l'uranium naturel irradie. Tailles et localisations optimales des usines

Energy Technology Data Exchange (ETDEWEB)

Thiriet, L [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires; Oger, C; Vaumas, P de [Saint-Gobain Nucleaire, 92 - Courbevoie (France)

1964-07-01

The aim of this paper is to help solve the problem of the selection of optimal sizes and sites for spent nuclear fuel processing plants associated with power capacity programmes already installed. Firstly, the structure of capital and running costs of irradiated natural uranium processing plants is studied, as well as the influence of plant sizes on these costs and structures. Shipping costs from the production site to the plant must also be added to processing costs. An attempt to reach a minimum cost for the production of a country or a group of countries must therefore take into account both the size and the location of the plants. The foreseeable shipping costs and their structure (freight, insurance, container cost and depreciation), for spent natural uranium are indicated. Secondly, for various annual spent fuel reprocessing programmes, the optimal sizes and locations of the plants are determined. The sensitivity of the results to the basic assumptions relative to processing costs, shipping costs, the starting up year of the plant programme and the length of period considered, is also tested. - this rather complex problem, of a combinative nature, is solved through dynamic programming methods. - It is shown that these methods can also be applied to the problem of selecting the optimal sizes and locations of processing plants for MTR type fuel elements, related to research reactor programmes, as well as to future plutonium element processing plants related to breeder reactors. Thirdly, the case where yearly extraction of the plutonium contained in the irradiated natural uranium is not compulsory is examined; some stockpiling of the fuel is then allowed some years, entailing delayed processing. The load factor of such plants is thus greatly improved with respect to that of plants where the annual plutonium demand is strictly satisfied. By including spent natural uranium stockpiling costs an optimal rhythm of introduction and optimal sizes for spent fuel

New processes for uranium isotope separation

International Nuclear Information System (INIS)

Vanstrum, P.R.; Levin, S.A.

1977-01-01

An overview of the status and prospects for processes other than gaseous diffusion, gas centrifuge, and separation nozzle for uranium isotope separation is presented. The incentive for the development of these processes is the increasing requirements for enriched uranium as fuel for nuclear power plants and the potential for reducing the high costs of enrichment. The latest nuclear power projections are converted to uranium enrichment requirements. The size and timing of the market for new enrichment processes are then determined by subtracting the existing and planned uranium enrichment capacities. It is estimated that to supply this market would require the construction of a large new enrichment plant of 9,000,000 SWU per year capacity, costing about $3 billion each (in 1976 dollars) about every year till the year 2000. A very comprehensive review of uranium isotope separation processes was made in 1971 by the Uranium Isotope Separation Review Ad Hoc Committee of the USAEC. Many of the processes discussed in that review are of little current interest. However, because of new approaches or remaining uncertainties about potential, there is considerable effort or continuing interest in a number of alternative processes. The status and prospects for attaining the requirements for competitive economics are presented for these processes, which include laser, chemical exchange, aerodynamic other than separation nozzle, and plasma processes. A qualitative summary comparison of these processes is made with the gaseous diffusion, gas centrifuge, and separation nozzle processes. In order to complete the overview of new processes for uranium isotope separation, a generic program schedule of typical steps beyond the basic process determination which are required, such as subsystem, module, pilot plant, and finally plant construction, before large-scale production can be attained is presented. Also the present value savings through the year 2000 is shown for various

Elimination of natural uranium and {sup 226}Ra from contaminated waters by rhizofiltration using Helianthus annuus L

Energy Technology Data Exchange (ETDEWEB)

Vera Tome, F. [Departamento de Fisica Aplicada, Facultad de Ciencias, Universidad de Extremadura, 06071 Badajoz (Spain)], E-mail: fvt@unex.es; Blanco Rodriguez, P. [Departamento de Fisica, Facultad de Ciencias, Universidad de Extremadura, 06071 Badajoz (Spain); Lozano, J.C. [Laboratorio de Radiactividad Ambiental, Facultad de Ciencias, Universidad de Salamanca, 37008 Salamanca (Spain)

2008-04-15

The elimination of natural uranium and {sup 226}Ra from contaminated waters by rhizofiltration was tested using Helianthus annuus L. (sunflower) seedlings growing in a hydroponic medium. Different experiments were designed to determine the optimum age of the seedlings for the remediation process, and also to study the principal way in which the radionuclides are removed from the solution by the sunflower roots. In every trial a precipitate appeared which contained a major fraction of the natural uranium and {sup 226}Ra. The results indicated that the seedlings themselves induced the formation of this precipitate. When four-week-old seedlings were exposed to contaminated water, a period of only 2 days was sufficient to remove the natural uranium and {sup 226}Ra from the solution: about 50% of the natural uranium and 70% of the {sup 226}Ra were fixed in the roots, and essentially the rest was found in the precipitate, with only very small percentages fixed in the shoots and left in solution.

The size distribution of dissolved uranium in natural waters

International Nuclear Information System (INIS)

Mann, D.K.; Wong, G.T.F.

1987-01-01

The size distribution of dissolved uranium in natural waters is poorly known. Some fraction of dissolved uranium is known to associate with organic matter which had a wide range of molecular weights. The presence of inorganic colloidal uranium has not been reported. Ultrafiltration has been used to quantify the size distribution of a number of elements, such as dissolved organic carbon, selenium, and some trace metals, in both the organic and/or the inorganic forms. The authors have applied this technique to dissolved uranium and the data are reported here

Process for recovery of uranium from wet process phosphoric acid

International Nuclear Information System (INIS)

Wiewiorowski, T.K.; Thornsberry, W.L. Jr.

1978-01-01

Process is claimed for the recovery of uranium from wet process phosphoric acid solution in which an organic extractant, containing uranium values and dissolved iron impurities and comprising a dialkylphosphoric acid and a trialkylphosphine oxide dissolved in a water immiscible organic solvent, is contacted with a substantially iron-free dilute aqueous phosphoric acid to remove said iron impurities. The removed impurities are bled from the system by feeding the resulting iron-loaded phosphoric acid to a secondary countercurrent uranium extraction operation from which they leave as part of the uranium-depleted acid raffinate. Also, process for recovering uranium in which the extractant, after it has been stripped of uranium values by aqueous ammonium carbonate, is contacted with a dilute aqueous acid selected from the group consisting of H 2 SO 4 , HCl, HNO 3 and iron-free H 3 PO 4 to improve the extraction efficiency of the organic extractant

Reactivity of Uranium and Ferrous Iron with Natural Iron Oxyhydroxides.

Science.gov (United States)

Stewart, Brandy D; Cismasu, A Cristina; Williams, Kenneth H; Peyton, Brent M; Nico, Peter S

2015-09-01

Determining key reaction pathways involving uranium and iron oxyhydroxides under oxic and anoxic conditions is essential for understanding uranium mobility as well as other iron oxyhydroxide mediated processes, particularly near redox boundaries where redox conditions change rapidly in time and space. Here we examine the reactivity of a ferrihydrite-rich sediment from a surface seep adjacent to a redox boundary at the Rifle, Colorado field site. Iron(II)-sediment incubation experiments indicate that the natural ferrihydrite fraction of the sediment is not susceptible to reductive transformation under conditions that trigger significant mineralogical transformations of synthetic ferrihydrite. No measurable Fe(II)-promoted transformation was observed when the Rifle sediment was exposed to 30 mM Fe(II) for up to 2 weeks. Incubation of the Rifle sediment with 3 mM Fe(II) and 0.2 mM U(VI) for 15 days shows no measurable incorporation of U(VI) into the mineral structure or reduction of U(VI) to U(IV). Results indicate a significantly decreased reactivity of naturally occurring Fe oxyhydroxides as compared to synthetic minerals, likely due to the association of impurities (e.g., Si, organic matter), with implications for the mobility and bioavailability of uranium and other associated species in field environments.

Aerodynamic isotope separation processes for uranium enrichment: process requirements

International Nuclear Information System (INIS)

Malling, G.F.; Von Halle, E.

1976-01-01

The pressing need for enriched uranium to fuel nuclear power reactors, requiring that as many as ten large uranium isotope separation plants be built during the next twenty years, has inspired an increase of interest in isotope separation processes for uranium enrichment. Aerodynamic isotope separation processes have been prominently mentioned along with the gas centrifuge process and the laser isotope separation methods as alternatives to the gaseous diffusion process, currently in use, for these future plants. Commonly included in the category of aerodynamic isotope separation processes are: (a) the separation nozzle process; (b) opposed gas jets; (c) the gas vortex; (d) the separation probes; (e) interacting molecular beams; (f) jet penetration processes; and (g) time of flight separation processes. A number of these aerodynamic isotope separation processes depend, as does the gas centrifuge process, on pressure diffusion associated with curved streamlines for the basic separation effect. Much can be deduced about the process characteristics and the economic potential of such processes from a simple and elementary process model. In particular, the benefit to be gained from a light carrier gas added to the uranium feed is clearly demonstrated. The model also illustrates the importance of transient effects in this class of processes

Uranium enrichment. Enrichment processes

International Nuclear Information System (INIS)

Alexandre, M.; Quaegebeur, J.P.

2009-01-01

Despite the remarkable progresses made in the diversity and the efficiency of the different uranium enrichment processes, only two industrial processes remain today which satisfy all of enriched uranium needs: the gaseous diffusion and the centrifugation. This article describes both processes and some others still at the demonstration or at the laboratory stage of development: 1 - general considerations; 2 - gaseous diffusion: physical principles, implementation, utilisation in the world; 3 - centrifugation: principles, elementary separation factor, flows inside a centrifuge, modeling of separation efficiencies, mechanical design, types of industrial centrifuges, realisation of cascades, main characteristics of the centrifugation process; 4 - aerodynamic processes: vortex process, nozzle process; 5 - chemical exchange separation processes: Japanese ASAHI process, French CHEMEX process; 6 - laser-based processes: SILVA process, SILMO process; 7 - electromagnetic and ionic processes: mass spectrometer and calutron, ion cyclotron resonance, rotating plasmas; 8 - thermal diffusion; 9 - conclusion. (J.S.)

Depleted uranium (DU) mobility in the natural environment

International Nuclear Information System (INIS)

Ragnarsdottir, K.V.

2002-01-01

In 1999 the Balkan's conflict lead NATO war planes to leave 10x10 3 kg of depleted uranium (DU) in the environment of Kosovo and neighbouring states (UNEP, 2001). DU behaves in the same manner in the environment as natural uranium and it can be traced with isotopic analysis due to the fact that DU has the isotopic composition of 0.2% 235 U and 99.8% 2 38 U as opposed to natural uranium which has 0.7% 2 35 U and 99.3% 2 38 U. DU is a waste product of the nuclear industry which enrich nuclear fuel by 2 35 U. Large stock piles of DU therefore exist in countries that produce nuclear energy and/or nuclear weapons. The DU is given to the weapons industry for free (or cheap) and has been a popular choice for armour penetrating arsenal due to the high density of uranium (19 g cm -3 ) and therefore its high penetrating power. Indeed the arsenal used in Kosovo consisted of DU penetrators that were shot from A-10 aeroplanes. They weigh roughly 300 g and have the shape of a fat 9 cm long pencil. (author)

Depleted uranium processing and fluorine extraction

International Nuclear Information System (INIS)

Laflin, S.T.

2010-01-01

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

10 CFR 40.66 - Requirements for advance notice of export shipments of natural uranium.

Science.gov (United States)

2010-01-01

... 10 Energy 1 2010-01-01 2010-01-01 false Requirements for advance notice of export shipments of natural uranium. 40.66 Section 40.66 Energy NUCLEAR REGULATORY COMMISSION DOMESTIC LICENSING OF SOURCE... natural uranium. (a) Each licensee authorized to export natural uranium, other than in the form of ore or...

Natural uranium

International Nuclear Information System (INIS)

Ammerich, Marc; Frot, Patricia; Gambini, Denis-Jean; Gauron, Christine; Moureaux, Patrick; Herbelet, Gilbert; Lahaye, Thierry; Pihet, Pascal; Rannou, Alain

2014-08-01

This sheet belongs to a collection which relates to the use of radionuclides essentially in unsealed sources. Its goal is to gather on a single document the most relevant information as well as the best prevention practices to be implemented. These sheets are made for the persons in charge of radiation protection: users, radioprotection-skill persons, labor physicians. Each sheet treats of: 1 - the radio-physical and biological properties; 2 - the main uses; 3 - the dosimetric parameters; 4 - the measurement; 5 - the protection means; 6 - the areas delimitation and monitoring; 7 - the personnel classification, training and monitoring; 8 - the effluents and wastes; 9 - the authorization and declaration administrative procedures; 10 - the transport; and 11 - the right conduct to adopt in case of incident or accident. This sheet deals specifically with natural uranium

PROCESS FOR PREPARING URANIUM METAL

Science.gov (United States)

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

1959-01-13

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

Uranium refining process using ion exchange membrane

International Nuclear Information System (INIS)

Yamaguchi, Akira

1977-01-01

As for the method of refining uranium ore being carried out in Europe and America at present, uranium ore is roughly refined at the mine sites to yellow cake, then this is transported to refineries and refined by dry method. This method has the following faults, namely the number of processes is large, it requires expensive corrosion-resistant materials because of high temperature treatment, and the impurities in uranium tend to increase. On the other hand, in case of EXCER method, treatment is carried out at low temperature, and high purity uranium can be obtained, but the efficiency of electrolytic reduction process is extremely low, and economically infeasible. In the wet refining method called PNC process, uranium tetrafluoride is produced from uranium ore without making yellow cake, therefore the process is rationalized largely, and highly economical. The electrolytic reduction process in this method was developed by Asahi Chemical Industry Co., Ltd. by constructing the pilot plant in Ningyotoge Mine. The ion exchange membrane, the electrodes, and the problems concerning the process and the engineering for commercial plants were investigated. The electrolytic reduction process, the pilot plant, the development of the elements of electrolytic cells, the establishment of analytical process, the measurement of the electrolytic characteristics, the demonstration operation, and the life time of the electrolytic diaphragm are reported. (Kako, I.)

Status Report from the United Kingdom [Processing of Low-Grade Uranium Ores

Energy Technology Data Exchange (ETDEWEB)

North, A A [Warren Spring Laboratory, Stevenage, Herts. (United Kingdom)

1967-06-15

The invitation to present this status report could have been taken literally as a request for information on experience gained in the actual processing of low-grade uranium ores in the United Kingdom, in which case there would have been very little to report; however, the invitation naturally was considered to be a request for a report on the experience gained by the United Kingdom of the processing of uranium ores. Lowgrade uranium ores are not treated in the United Kingdom simply because the country does not possess any known significant deposits of uranium ore. It is of interest to record the fact that during the nineteenth century mesothermal vein deposits associated with Hercynian granite were worked at South Terras, Cornwall, and ore that contained approximately 100 tons of uranium oxide was exported to Germany. Now only some 20 tons of contained uranium oxide remain at South Terras; also in Cornwall there is a small number of other vein deposits that each hold about five tons of uranium. Small lodes of uranium ore have been located in the southern uplands of Scotland; in North Wales lower palaeozoic black shales have only as much as 50 to 80 parts per million of uranium oxide, and a slightly lower grade carbonaceous shale is found near the base of the millstone grit that occurs in the north of England. Thus the experience gained by the United Kingdom has been of the treatment of uranium ores that occur abroad.

Processing of uranium-containing coal

International Nuclear Information System (INIS)

Cordero Alvarez, M.

1987-01-01

A direct storage of uranium-bearing coal requires the processing of large amounts of raw materials while lacking guarantee of troublefree process cycles. With the example of an uranium-bearing bituminous coal from Stockheim, it was aimed at the production of an uranium ore concentrate by means of mechanical, thermal and chemical investigations. Above all, amorphous pitch blende was detected as a uranium mineralization which occurs homogeneously distributed in the grain size classes of the comminuted raw material with particle diameters of a few μm and, after the combustion, enriches in the field of finest grain of the axis. Heterogeneous and solid-state reactions in the thermal decarburization above 700deg C result in the development of hardly soluble uranium oxides and and calcium uranates as well as in enclosures in mineral glass. Thus, the pre-enrichment has to take place in a temperature range below 600deg C. By means of a sorting classification of the ash at ± 2.0 mm, it is possible to achieve an enrichment of up to factor 15 for a mineral of a mainly low carbonate content and, for a mineral of a rich carbonate content, up to the factor 4. The separation of the uranium from the concentrates produced is possible with a yield of 95% by means of leaching with sulphuric acid at a temperature of 20deg C. As far as their reproducibility was concerned, the laboratory tests were verified on a semi-industrial scale. A processing method is suggested on the basis of the data obtained. (orig.) [de

Distinction between natural and depleted uranium using instrumental neutron activation analysis

International Nuclear Information System (INIS)

Haddad, Kh.

2008-01-01

A convenient method to discriminate between natural and depleted uranium samples was developed in this work. Traces of natural and depleted uranium were irradiated separately and the ratios of 95 Zr/ 103 Ru, 239 Np/ 95 Zr, 239 Np/ 103 Ru were measured. The results show that these ratios can be used as indicators of the uranium isotopic composition of the sample. These ratios are independent of the secular equilibrium of the 238 U with its daughters in the sample and indicate the isotopic composition for trace amounts. Date and truffle samples has been analysed also using this method. Results show that the uranium content in this product was less than the detection limit.(author)

An evaluation of the dissolution process of natural uranium ore as an analogue of nuclear fuel

International Nuclear Information System (INIS)

Stern, V.H.

1991-08-01

The assumption of congruent dissolution of uraninite as a mechanism for the dissolution behaviour of spent fuel was critically examined with regard to the fate of toxic radionuclides. The fission and daughter products of uranium are typically present in spent unreprocessed fuel rods in trace abundances. The principles of trace element geochemistry were applied in assessing the behaviour of these radionuclides during fluid/solid interactions. It is shown that the behaviour of radionuclides in trace abundances that reside in the crystal structure can be better predicted from the ionic properties of these nuclides rather than from assuming that they are controlled by the dissolution of uraninite. Geochemical evidence from natural uranium ore deposits (Athabasca Basin, Northern Territories of Australia, Oklo) suggests that in most cases the toxic radionuclides are released from uraninite in amounts that are independent of the solution behaviour of uranium oxide. Only those elements that have ionic and thus chemical properties similar to U 4+ , such as plutonium, americium, cadmium, neptunium and thorium can be satisfactorily modelled by the solution properties of uranium dioxide and then only if the environment is reducing. (84 refs., 7 tabs.)

Natural uranium toxicology - evaluation of internal contamination in man

International Nuclear Information System (INIS)

Chalabreysse, J.

1968-01-01

After reminding the physical and chemical properties of natural uranium which might affect its toxicology, a comprehensive investigation upon natural uranium metabolism and toxicity and after applying occupational exposure standards to this particular poison, it has been determined, from accident reports and human experience reported in the related literature, a series of formulae obtained by theoretical mathematical development giving principles for internal contamination monitoring and disclosure by determining uranium in the urine of occupationally exposed individuals. An assay is performed to determine individual internal contamination according to the various contamination cases. The outlined purposes, mainly practical, required some options and extrapolations. The proposed formula allows a preliminary approach and also to determine shortly a contamination extent or to discuss the systematical urinalysis results as compared with individual radio-toxicology monitoring professional standards. (author) [fr

Operating experience in processing of differently sourced deeply depleted uranium oxide and production of deeply depleted uranium metal ingots

International Nuclear Information System (INIS)

Manna, S.; Ladola, Y.S.; Sharma, S.; Chowdhury, S.; Satpati, S.K.; Roy, S.B.

2009-01-01

Uranium Metal Plant (UMP) of BARC had first time experience on production of three Depleted Uranium Metal (DUM) ingots of 76kg, 152kg and 163kg during March 1991. These ingots were produced by processing depleted uranyl nitrate solution produced at Plutonium Plant (PP), Trombay. In recent past Uranium Metal Plant (UMP), Uranium Extraction Division (UED), has been assigned to produce tonnage quantity of Deeply DUM (DDUM) from its oxide obtained from PP, PREFRE and RMP, BARC. This is required for shielding the high radioactive source of BHABHATRON Tele-cobalt machine, which is used for cancer therapy. The experience obtained in processing of various DDU oxides is being utilized for design of large scale DDU-metal plant under XIth plan project. The physico- chemical characteristics like morphology, density, flowability, reactivity, particle size distribution, which are having direct effect on reactivity of the powders of the DDU oxide powder, were studied and the shop-floor operational experience in processing of different oxide powder were obtained and recorded. During campaign trials utmost care was taken to standardized all operating conditions using the same equipment which are in use for natural uranium materials processing including safety aspects both with respect to radiological safety and industrial safety. Necessary attention and close monitoring were specially arranged and maintained for the safety aspects during the trial period. In-house developed pneumatic transport system was used for powder transfer and suitable dust arresting system was used for reduction of powder carry over

The measurement of natural uranium in urine by fluorometry

International Nuclear Information System (INIS)

Kramer, G.H.; Johnson, J.R.; Green, W.

1984-02-01

The fluorometric method of measuring natural uranium in urine that is currently used by the Bioassay Laboratory at Chalk River Nuclear Laboratories has been tested, optimized and documented. The method, which measures the fluorescence of uranium in a fused sodium fluoride pellet, has been shown to be quench independent and is routinely used to measure uranium concentrations in the range of 1 μg/L to 90 μg/L. The fluorimeter has a dynamic range of 0.2 μg/L to 200 μg/L

Uranium/plutonium and uranium/neptunium separation by the Purex process using hydroxyurea

International Nuclear Information System (INIS)

Zhu Zhaowu; He Jianyu; Zhang Zefu; Zhang Yu; Zhu Jianmin; Zhen Weifang

2004-01-01

Hydroxyurea dissolved in nitric acid can strip plutonium and neptunium from tri-butyl phosphate efficiently and has little influence on the uranium distribution between the two phases. Simulating the 1B contactor of the Purex process by hydroxyurea with nitric acid solution as a stripping agent, the separation factors of uranium/plutonium and uranium/neptunium can reach values as high as 4.7 x 10 4 and 260, respectively. This indicates that hydroxyurea is a promising salt free agent for uranium/plutonium and uranium/neptunium separations. (author)

Uranium manufacturing process employing the electrolytic reduction method

International Nuclear Information System (INIS)

Oda, Yoshio; Kazuhare, Manabu; Morimoto, Takeshi.

1986-01-01

The present invention related to a uranium manufacturing process that employs the electrolytic reduction method, but particularly to a uranium manufacturing process that employs an electrolytic reduction method requiring low voltage. The process, in which uranium is obtained by means of the electrolytic method and with uranyl acid as the raw material, is prior art

Studies on uranium ore processing

International Nuclear Information System (INIS)

Kim, C.H.; Park, S.W.; Lim, J.K.; Chung, M.K.

1981-01-01

Chemical and chemical engineering techniques of the uranium ore processing established by France COGEMA (Compagnie Generale des Matieres Nucleaires) have been comprehensively reviewed in preparation for successful test operation of the pilot plant to be completed by the end of 1981. It was found that the amount of sulfuric acid (75 Kg/t, ore) and sodium chlorate (2.5 Kg/t, ore) recommended by COGEMA should be increased up to 100 Kg/t, ore and 10 Kg/t, ore respectively to obtain satisfactory leach of uranium for some ore samples produced at the different pits of Goesan uranium mine. Conditions of the other processes such as solvent extraction, stripping, and precipitation of yellow cake were generally agreed with the results of intensive studies done by this laboratory

Uranium bed oxidation vacuum process system

International Nuclear Information System (INIS)

McLeland, H.L.

1977-01-01

Deuterium and tritium gases are occluded in uranium powder for release into neutron generator tubes. The uranium powder is contained in stainless steel bottles, termed ''beds.'' If these beds become damaged, the gases must be removed and the uranium oxidized in order not to be flammable before shipment to ERDA disposal grounds. This paper describes the system and methods designed for the controlled degassing and oxidation process. The system utilizes sputter-ion, cryo-sorption and bellows pumps for removing the gases from the heated source bed. Removing the tritium gas is complicated by the shielding effect of helium-3, a byproduct of tritium decay. This effect is minimized by incremental pressure changes, or ''batch'' processing. To prevent runaway exothermic reaction, oxidation of the uranium bed is also done incrementally, or by ''batch'' processing, rather than by continuous flow. The paper discusses in detail the helium-3 shielding effect, leak checks that must be made during processing, bed oxidation, degree of gas depletion, purity of gases sorbed from beds, radioactivity of beds, bed disposal and system renovation

Uranium recovery from wet process phosphoric acid

International Nuclear Information System (INIS)

1980-01-01

In the field of metallurgy, specifically processes for recovering uranium from wet process phosphoric acid solution derived from the acidulation of uraniferous phosphate ores, problems of imbalance of ion exchange agents, contamination of recycled phosphoric acid with process organics and oxidizing agents, and loss and contamination of uranium product, are solved by removing organics from the raffinate after ion exchange conversion of uranium to uranous form and recovery thereof by ion exchange, and returning organics to the circuit to balance mono and disubstituted ester ion exchange agents; then oxidatively stripping uranium from the agent using hydrogen peroxide; then after ion exchange recovery of uranyl and scrubbing, stripping with sodium carbonate and acidifying the strip solution and using some of it for the scrubbing; regenerating the sodium loaded agent and recycling it to the uranous recovery step. Economic recovery of uranium as a by-product of phosphate fertilizer production is effected. (author)

Filtration aids in uranium ore processing

International Nuclear Information System (INIS)

Ford, H.L.; Levine, N.M.; Risdon, A.R.

1975-01-01

A process of improving the filtration efficiency and separation of uranium ore pulps obtained by carbonate leaching of uranium ore which comprises treating said ore pulps with an aqueous solution of hydroxyalkyl guar selected from the group consisting of hydroxyethyl and hydroxypropyl guar in the amount of 0.1 and 2.0 pounds of hydroxyalkyl guar per ton of uranium ore

Process for recovering a uranium containing concentrate and purified phosphoric acid from a wet process phosphoric acid containing uranium

International Nuclear Information System (INIS)

Weterings, C.A.M.; Janssen, J.A.

1985-01-01

A process is claimed for recovering from a wet process phosphoric acid which contains uranium, a uranium containing concentrate and a purified phosphoric acid. The wet process phosphoric acid is treated with a precipitant in the presence of a reducing agent and an aliphatic ketone

Process for recovering a uranium containing concentrate and purified phosphoric acid from a wet process phosphoric acid containing uranium

Energy Technology Data Exchange (ETDEWEB)

Weterings, C.A.M.; Janssen, J.A.

1985-04-30

A process is claimed for recovering from a wet process phosphoric acid which contains uranium, a uranium containing concentrate and a purified phosphoric acid. The wet process phosphoric acid is treated with a precipitant in the presence of a reducing agent and an aliphatic ketone.

Influence of Uranium on Bacterial Communities: A Comparison of Natural Uranium-Rich Soils with Controls

Science.gov (United States)

Mondani, Laure; Benzerara, Karim; Carrière, Marie; Christen, Richard; Mamindy-Pajany, Yannick; Février, Laureline; Marmier, Nicolas; Achouak, Wafa; Nardoux, Pascal; Berthomieu, Catherine; Chapon, Virginie

2011-01-01

This study investigated the influence of uranium on the indigenous bacterial community structure in natural soils with high uranium content. Radioactive soil samples exhibiting 0.26% - 25.5% U in mass were analyzed and compared with nearby control soils containing trace uranium. EXAFS and XRD analyses of soils revealed the presence of U(VI) and uranium-phosphate mineral phases, identified as sabugalite and meta-autunite. A comparative analysis of bacterial community fingerprints using denaturing gradient gel electrophoresis (DGGE) revealed the presence of a complex population in both control and uranium-rich samples. However, bacterial communities inhabiting uraniferous soils exhibited specific fingerprints that were remarkably stable over time, in contrast to populations from nearby control samples. Representatives of Acidobacteria, Proteobacteria, and seven others phyla were detected in DGGE bands specific to uraniferous samples. In particular, sequences related to iron-reducing bacteria such as Geobacter and Geothrix were identified concomitantly with iron-oxidizing species such as Gallionella and Sideroxydans. All together, our results demonstrate that uranium exerts a permanent high pressure on soil bacterial communities and suggest the existence of a uranium redox cycle mediated by bacteria in the soil. PMID:21998695

Uranium ore processing

International Nuclear Information System (INIS)

Ritcey, G.M.; Haque, K.E.; Lucas, B.H.; Skeaff, J.M.

1983-01-01

The authors have developed a complete method of recovering separately uranium, thorium and radium from impure solids such as ores, concentrates, calcines or tailings containing these metals. The technique involves leaching, in at least one stage. The impure solids in finely divided form with an aqueous leachant containing HCl and/or Cl 2 until acceptable amounts of uranium, thorium and radium are dissolved. Uranium is recovered from the solution by solvent extraction and precipitation. Thorium may also be recovered in the same manner. Radium may be recovered by at least one ion exchange, absorption and precipitation. This amount of iron in the solution must be controlled before the acid solution may be recycled for the leaching process. The calcine leached in the first step is prepared in a two stage roast in the presence of both Cl 2 and a metal sulfide. The first stage is at 350-450 0 and the second at 550-700 0

A process for uranium recovery in phosphoric acid

International Nuclear Information System (INIS)

Duarte Neto, J.

1984-01-01

Results are presented about studies carried out envisaging the development of a process for uranium recovery from phosphoric acid, produced from the concentrate obtained from phosphorus-uraniferous mineral from Itataia mines (CE, Brazil). This process uses a mixture of DEPA-TOPO as extractant and the extraction cycle involves the following stages: acid pre-treatment; adjustment of the oxidation potential so to ensure that all uranium is hexavalent; extraction of uranium from the acid; screening of the solvent to remove undesirable impurities; uranium re-extraction and precipitation; solvent recovery. A micro-pilot plant for continuous processing was built up. Data collected showed that uranium can be recovered with an yield greater than 99%, thus proving the feasibility of the process and encouraging the construction of a bigger scale plant. (Author) [pt

Natural uranium and 226Ra in bottled potable waters of Argentina

International Nuclear Information System (INIS)

Bomben, Ana M.; Palacios, Miguel A.

2001-01-01

This paper presents the results obtained of the measurement of the natural uranium and 226 Ra concentrations carried out on 345 drinking water samples coming from different provinces of Argentina. The samples were collected from tap water systems and private wells. Six bottled mineral waters samples, selected from those most extensively consumed, were also analyzed. The natural uranium concentration was determined by a fluorimetric procedure and 226 Ra by the 222 Rn emanation technique and liquid scintillation counting. Values ranging from 0,03 to 50 μg L -1 of natural uranium and concentrations up to 22 mBq L -1 were found in the drinking water samples analyzed. Natural uranium concentrations from 0,04 to 3,8 μg L -1 and 226 Ra concentrations up to 2,4 mBq L -1 were measured in the bottled mineral waters samples. Based on the water intake rate and the measured concentrations of both radionuclides analyzed, an annual collective effective dose of 1,5 man Sv and an average committed effective dose of 0,5 μSv a -1 , were calculated for the City of Buenos Aires inhabitants. (author)

Distribution of natural radionuclides of uranium and thorium series in the process of artesian water treatment for drinking consumption

International Nuclear Information System (INIS)

Grashchenko, S.M.; Gritchenko, Z.G.; Shishkunova, L.V.

1997-01-01

Distribution of natural radionuclides of uranium and thorium series during the treatment of artesian water for drinking consumption is studied using vacuum-emanation and gamma spectrometry methods. During the water treatment hydroxide precipitates are produced at the station, which are isolated using a sand filter, radium isotopes being coprecipitated alongside with them. As a result of this radioactive waste is accumulated at the station, radium isotope concentration in it being equivalent to radium isotope concentration in uranium-thorium ores with 0:11% uranium and 0.56% thorium content. radium isotope concentration in water, delivered to the user do not exceed the established domestic normatives do not exceed the established domestic normatives

Oxidation-extraction of uranium from wet-process phosphoric acid

International Nuclear Information System (INIS)

Lawes, B.C.

1985-01-01

The invention involves an improvement to the reductive stripping process for recovering uranium values from wet-process phosphoric acid solution, where uranium in the solution is oxidized to uranium (VI) oxidation state and then extracted from the solution by contact with a water immiscible organic solvent, by adding sufficient oxidant, hydrogen peroxide, to obtain greater than 90 percent conversion of the uranium to the uranium (VI) oxidation state to the phosphoric acid solution and simultaneously extracting the uranium (VI)

Uranium in a recent phosphorite formation process

Energy Technology Data Exchange (ETDEWEB)

Baturin, G N; Dubinchuk, V I; Kochenov, A V

1986-01-01

Uranium behaviour in the process of nowadays phosphorite formation in the sediments of Namibia shelf is considered. The material collected during the 3-d trip of the research vessel ''Akademik Kurchatov'' and 26-th trip of the research vessel ''Mikhail Lomonosov'' is used. The samples from three geological stations 2046, 2047 and 2048 from the depths of 78-87 m have been investigated. Each sample (mass from 0.2 to 0.3 kg) is composed of several samples representing unified genetic series: holocene diatomic silts enclosing phosphorites - phosphatized silts - phosphorite concretions. Uranium has been determined by the X-ray spectral method; phosphorus, organic carbon and other components - by the chemical analysis. Uranium forms investigated by the combination of methods of electron microscopy, microdiffraction, microradioautography and microsounding. Uranium content in nowadays phosphorites at the shelf is 3-106 g/t. Uranium accumulation in phosphorites at the initial stages of their formation is controlled by its content in host sediments. In the course of litification of diagenetic phosphate concretions the uranium content in them varies from 40 to 80 g/t. The uranium concentration process in phosphorites is accompanied by formation of independent mineral phases of uranium oxide and ningyoite type.

Liquid membrane process for uranium recovery

International Nuclear Information System (INIS)

Valint, P.L. Jr.

1982-01-01

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

Case history of natural analogue research on sandstone type uranium occurrences, Japan

International Nuclear Information System (INIS)

Sakamaki, Y.; Kanai, Y.

1991-01-01

Previous fundamental studies on the ore genesis of uranium occurrences chiefly in Cenozoic sandstone formations in Japan, have been re-examined as the case history on natural analogue of radionuclides in high-level radioactive wastes (HLRW). Two principal mode of occurrences have been distinguished among Cenozoic uranium localities in Japan. In the Setouchi (Inland Sea) subregion, hot-spots are found in lacustrine to shallow sea facies of calm environment, corresponding to the first stage of formation of tectonic basins. As observed in Ningyo-toge and Tono area, stratabound ore bodies are generally arranged into paleo-channels. Another type of sporadic uranium indications are found within collapse basins in the 'Green-tuff' subregion, where intense volcanisms and block movements had been taken places throughout Middle miocene age. Well-developed fractures were to be favorable paths for uraniferous groundwater, as well as the suitable site for deposition of uranium. In both cases, the source material of uranium is granitic basement. Under oxidizing environment, uranium anomalies have been occasionally detected in surface- or fracture waters which passing through decomposed granite. In contrast to the behavior of uranium, one of the adequate analogues for mobile nuclides, thorium and REE are relatively immobile even under the same geologic and geochemical circumstances. In ore horizon, where reducing condition has still been kept, geochronological age of tetravalent uranium mineral is in concordance with the age of the host rock. Analysis of structural control shows that the principal factors for uranium concentration are the layout of redox front related to paleo-water tables. 234U/238U disequilibrium method has been proved to be the powerful tool for detecting mobility of uranium in the host rock throughout diagenesis and weathering process. The result of field and laboratory works on this is reported as an example. (author)

Ore-processing technology and the uranium supply outlook

International Nuclear Information System (INIS)

James, H.E.; Simonsen, H.A.

1978-01-01

The subject is covered in sections, as follows: the resource base (uranium content of rocks, regional distribution of Western World uranium); ore types (distribution of Western World uranium, by ore types, response to ore-processing); constraints on expansion in traditional uranium areas (defined for this paper as the sandstone deposits of the U.S.A. and the quartz-pebble conglomerates of the Witwatersrand and Elliot Bay areas, all other deposits being referred to as new uranium areas). Sections then follow dealing in detail with the processing of deposits in U.S.A., South Africa, Canada, Niger, Australia, South West Africa, Greenland. More general sections follow on: shale, lignite and coal deposits, calcrete deposits. Finally, there are sections on: uranium as a by-product; uranium from very low-grade resources; constraints on expansion rate for production facilities. (U.K.)

Characteristics of the natural uranium ingots developed in IPEN - CNEN/SP

International Nuclear Information System (INIS)

Soares, M.C.B.; Koshimizu, S.

1990-01-01

The natural uranium consists of two primary isotopes, the U sup(235) (0,7%) and the U sup(238) (99,3%). The isotopic separation carried out in order to obtain enriched uranium, generates a by-product called depleted uranium, which can be applied for industrial uses. The most singular property, from engineering standpoint, is its high density. When the density is the only important factor, the uranium has great advantage over other heavy metals related to economic and technical considerations. Among some applications of uranium are aircraft and missile counterweights, kinetics energy penetrators, radiation shielding, gyro rotors and oil-well sinker bars. The uranium ingot fabrication is done by direct reduction of UF, with magnesium, without remelting. The microstructure of as-cast uranium is, as in the other as-cast, formed by coarse and. (author)

Glances on uranium. From uranium in the earth to electric power

International Nuclear Information System (INIS)

Valsardieu, C.

1995-01-01

This book is a technical, scientific and historical analysis of the nuclear fuel cycle from the origin of uranium in the earth and the exploitation of uranium ores to the ultimate storage of radioactive wastes. It comprises 6 chapters dealing with: 1) the different steps of uranium history (discovery, history of uranium chemistry, the radium era, the physicists and the structure of matter, the military uses, the nuclear power, the uranium industry and economics), 2) the uranium in nature (nuclear structure, physical-chemical properties, radioactivity, ores, resources, cycle, deposits), 3) the sidelights on uranium history (mining, prospecting, experience, ore processing, resources, reserves, costs), 4) the uranium in the fuel cycle, energy source and industrial product (fuel cycle, fission, refining, enrichment, fuel processing and reprocessing, nuclear reactors, wastes management), 5) the other energies in competition and the uranium market (other uranium uses, fossil fuels and renewable energies, uranium market), and 6) the future of uranium (forecasting, ecology, economics). (J.S.)

226Ra and natural uranium in egyptian bottled mineral waters

International Nuclear Information System (INIS)

Higgy, R.H.

2000-01-01

Concentration levels of 226 Ra and natural uranium have been analysed bottled mineral water commercially available in egypt. 226 Ra was determined by applying a chemical procedure in which Ra was coprecipitated with Ba as sulphate. The precipitate was then dissolved with EDTA and then measured by liquid scintillation system, after mixing with a scintillation cocktail. Natural uranium was determined by applying a chemical procedure for uranium extraction using MIBK and then measured using laser fluorimeter system. The concentration values obtained were compared with concentrations reported by other countries and with reference values accepted for drinking water. Based on the consumption rate and the measured concentrations, the collective committed effective doses were calculated. In addition, Ca, Mg and Na were measured using Icp system and compared with some worldwide values

Process for recovering uranium

Science.gov (United States)

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

1959-03-24

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

Exposure pathways and health effects associated with chemical and radiological toxicity of natural uranium: a review.

Science.gov (United States)

Brugge, Doug; de Lemos, Jamie L; Oldmixon, Beth

2005-01-01

Natural uranium exposure derives from the mining, milling, and processing of uranium ore, as well as from ingestion of groundwater that is naturally contaminated with uranium. Ingestion and inhalation are the primary routes of entry into the body. Absorption of uranium from the lungs or digestive track is typically low but can vary depending on compound specific solubility. From the blood, two-thirds of the uranium is excreted in urine over the first 24 hours and up to 80% to 90% of uranium deposited in the bone leaves the body within 1.5 years. The primary health outcomes of concern documented with respect to uranium are renal, developmental, reproductive, diminished bone growth, and DNA damage. The reported health effects derive from experimental animal studies and human epidemiology. The Lowest Observed Adverse Effect Level (LOAEL) derived from animal studies is 50 microg/m3 for inhalation and 60 ug/kg body weight/day for ingestion. The current respiratory standard of the Occupational Safety and Health Administration (OSHA), 50 microg/m3, affords no margin of safety. Considering the safety factors for species and individual variation, the ingestion LOAEL corresponds to the daily consumption set by the World Health Organization Drinking Water Standard at 2 microg/L. Based on economic considerations, the United States Environmental Protection Agency maximum contaminant level is 30 microg/L. Further research is needed, with particular attention on the impact of uranium on indigenous populations, on routes of exposure in communities near uranium sites, on the combined exposures present at many uranium sites, on human developmental defects, and on health effects at or below established exposure standards.

Uranium industry in the USSR

International Nuclear Information System (INIS)

Nikipelov, B.V.; Chernov, A.G.

1990-01-01

A brief historical account of the Soviet production of natural and enriched uranium is given. The geological and geographical location of major uranium deposits are mentioned. The processing of natural ores including in-situ leaching (ISL) is also briefly described. Gas centrifuges play a large part in uranium enrichment. The role of Techsnabexport for the export of nuclear materials is explained

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.

Comparative analysis of calculations and experiment for uranium-graphite lattices with natural and slightly-enriched uranium

International Nuclear Information System (INIS)

Khrennikov, N.N.; Shchukin, A.V.

1988-01-01

Three sets of experiments carried out at different times and in different laboratories on measuring the material parameter for uranium-graphite lattices using natural and slightly enriched uranium are analyzed. Comparison with the calculations by the TRIFOGR and MCU (the Monte Carlo method) codes reveals resonable agreement between the calculation and experiment (of the order of 0.4% in K eff ). 17 refs.; 3 tabs

Radioactivity of uranium production cycle facilities in the Czech Republic compared to the natural environment

International Nuclear Information System (INIS)

Matolin, M.

2002-01-01

Forty-five years (1946-1990) of intensive uranium exploration and exploitation in the Czech Republic led to mining at 64 uranium deposits. These mining and milling activities left numerous accumulations of waste rock material in the landscape. The radioactivity of these man-made accumulations was measured and compared to the natural radiation environment. Waste rock dumps at the uranium deposits Pribram, Rozna, Jachymov, Straz-Hamr and deposits in the Zelezne Hory area show surface gamma dose rates mostly in the range of 200-1000 nGy/h, with a uranium concentration 10-100 ppm eU. An extremely high radioactivity of 3000-4200 nGy/h was detected at the extensive uranium processing tailings impoundments at Straz. Terrestrial gamma dose rate of regional geological units in the Czech Republic is in the range of 6-245 nGy/h. Reclamation and recultivation of dumps, control of their radioactivity and restriction of their accessibility are the major measures introduced to protect the public. (author)

The Bare Critical Assembly of Natural Uranium and Heavy Water

Energy Technology Data Exchange (ETDEWEB)

Popovic, D [Boris Kidric Institute of Nuclear Sciences, Vinca, Belgrade (Yugoslavia)

1958-07-01

The first reactor built in Yugoslavia was the bare zero energy heavy water and natural uranium assembly at the Boris Kidric Institute of Nuclear Sciences, Belgrade. The reactor went critical on April 29, 1958. The possession of four tons of natural uranium metal and the temporary availability of seven tons of heavy water encouraged the staff of the Institute to build a critical assembly. A critical assembly was chosen, rather than high flux reactor, because the heavy water was available only temporarily. Besides, a 10 MW, enriched uranium, research reactor is being built at the same Institute and should be ready for operation late this year. It was supposed that the zero energy reactor would provide experience in carrying out critical experiments, operational experience with nuclear reactors, and the possibility for an extensive program in reactor physics. (author)

Solubility of airborne uranium samples from uranium processing plant

International Nuclear Information System (INIS)

Kravchik, T.; Oved, S.; Sarah, R.; Gonen, R.; Paz-Tal, O.; Pelled, O.; German, U.; Tshuva, A.

2005-01-01

Full text: During the production and machining processes of uranium metal, aerosols might be released to the air. Inhalation of these aerosols is the main route of internal exposure of workers. To assess the radiation dose from the intake of these uranium compounds it is necessary to know their absorption type, based on their dissolution rate in extracellular aqueous environment of lung fluid. The International Commission on Radiological Protection (ICRP) has assigned UF4 and U03 to absorption type M (blood absorption which contains a 10 % fraction with an absorption rate of 10 minutes and 90 % fraction with an absorption rate of 140 fays) and UO2 and U3O8 to absorption type S (blood absorption rate with a half-time of 7000 days) in the ICRP-66 model.The solubility classification of uranium compounds defined by the ICRP can serve as a general guidance. At specific workplaces, differences can be encountered, because of differences in compounds production process and the presence of additional compounds, with different solubility characteristics. According to ICRP recommendations, material-specific rates of absorption should be preferred to default parameters whenever specific experimental data exists. Solubility profiles of uranium aerosols were determined by performing in vitro chemical solubility tests on air samples taken from uranium production and machining facilities. The dissolution rate was determined over 100 days in a simultant solution of the extracellular airway lining fluid. The filter sample was immersed in a test vial holding 60 ml of simultant fluid, which was maintained at a 37 o C inside a thermostatic bath and at a physiological pH of 7.2-7.6. The test vials with the solution were shaken to simulate the conditions inside the extracellular aqueous environment of the lung as much as possible. The tests indicated that the uranium aerosols samples taken from the metal production and machining facilities at the Nuclear Research Center Negev (NRCN

Processing of Sierra Albarrana uranium ores

International Nuclear Information System (INIS)

Gutierrez Jodra, L.; Perez Luina, A.; Perarnau, M.

1960-01-01

Uranium recovery by hydrometallurgy from brannerite, found in Hornachuelos (Cordoba) is described. It has been studied the acid and alkaline leaching and salt roasting, proving as more satisfactory the acid leaching. Besides the uranium solubilization by acid leaching, is described the further process to obtain pure uranyl nitrate. (Author)

Extraction of uranium from seawater: chemical process and plant design feasibility study

International Nuclear Information System (INIS)

Campbell, M.H.; Frame, J.M.; Dudey, N.D.; Kiel, G.R.; Mesec, V.; Woodfield, F.W.; Binney, S.E.; Jante, M.R.; Anderson, R.C.; Clark, G.T.

1979-02-01

A major assessment was made of the uranium resources in seawater. Several concepts for moving seawater to recover the uranium were investigated, including pumping the seawater and using natural ocean currents or tides directly. The optimal site chosen was on the southeastern Puerto Rico coast, with the south U.S. Atlantic coast as an alternate. The various processes for extracting uranium from seawater were reviewed, with the adsorption process being the most promising at the present time. Of the possible adsorbents, hydrous titanium oxide was found to have the best properties. A uranium extraction plant was conceptually designed. Of the possible methods for contacting the seawater with the adsorbent, a continuous fluidized bed concept was chosen as most practical for a pumped system. A plant recovering 500 tonnes of U 3 O 8 per year requires 5900 cubic meters per second of seawater to be pumped through the adsorbent beds for a 70% overall recovery efficiency. Total cost of the plant was estimated to be about $6.2 billion. A computer model for the process was used for parametric sensitivity studies and economic projections. Several design case variations were developed. Other topics addressed were the impact of co-product recovery, environmental considerations, etc

Extraction of uranium from seawater: chemical process and plant design feasibility study

Energy Technology Data Exchange (ETDEWEB)

Campbell, M.H.; Frame, J.M.; Dudey, N.D.; Kiel, G.R.; Mesec, V.; Woodfield, F.W.; Binney, S.E.; Jante, M.R.; Anderson, R.C.; Clark, G.T.

1979-02-01

A major assessment was made of the uranium resources in seawater. Several concepts for moving seawater to recover the uranium were investigated, including pumping the seawater and using natural ocean currents or tides directly. The optimal site chosen was on the southeastern Puerto Rico coast, with the south U.S. Atlantic coast as an alternate. The various processes for extracting uranium from seawater were reviewed, with the adsorption process being the most promising at the present time. Of the possible adsorbents, hydrous titanium oxide was found to have the best properties. A uranium extraction plant was conceptually designed. Of the possible methods for contacting the seawater with the adsorbent, a continuous fluidized bed concept was chosen as most practical for a pumped system. A plant recovering 500 tonnes of U/sub 3/O/sub 8/ per year requires 5900 cubic meters per second of seawater to be pumped through the adsorbent beds for a 70% overall recovery efficiency. Total cost of the plant was estimated to be about $6.2 billion. A computer model for the process was used for parametric sensitivity studies and economic projections. Several design case variations were developed. Other topics addressed were the impact of co-product recovery, environmental considerations, etc.

Process development study on production of uranium metal from monazite sourced crude uranium tetra-fluoride

International Nuclear Information System (INIS)

Chowdhury, S; Satpati, S.K.; Hareendran, K.N.; Roy, S.B.

2014-01-01

Development of an economic process for recovery, process flow sheet development, purification and further conversion to nuclear grade uranium metal from the crude UF 4 has been a technological challenge and the present paper, discusses the same.The developed flow-sheet is a combination of hydrometallurgical and pyrometallurgical processes. Crude UF 4 is converted to uranium di-oxide (UO 2 ) by chemical conversion route and UO 2 produced is made fluoride-free by repeated repulping, followed by solid liquid separation. Uranium di-oxide is then purified by two stages of dissolution and suitable solvent extraction methods to get uranium nitrate pure solution (UNPS). UNPS is then precipitated with air diluted ammonia in a leak tight stirred vessel under controlled operational conditions to obtain ammonium di-uranate (ADU). The ADU is then calcined and reduced to produce metal grade UO 2 followed by hydro-fluorination using anhydrous hydrofluoric acid to obtain metal grade UF 4 with ammonium oxalate insoluble (AOI) content of 4 is essential for critical upstream conversion process. Nuclear grade uranium metal ingot is finally produced by metallothermic reduction process at 650℃ in a closed vessel, called bomb reactor. In the process, metal-slag separation plays an important role for attaining metal purity as well as process yield. Technological as well economic feasibility of indigenously developed process for large scale production of uranium metal from the crude UF 4 has been established in Bhabha Atomic Research Centre (BARC), India

Refining of crude uranium by solvent extraction for production of nuclear pure uranium metal

International Nuclear Information System (INIS)

Gupta, S.K.; Manna, S.; Singha, M.; Hareendran, K.N.; Chowdhury, S.; Satpati, S.K.; Kumar, K.

2007-01-01

Uranium is the primary fuel material for any nuclear fission energy program. Natural uranium contains only 0.712% of 235 U as fissile constituent. This low concentration of fissile isotope in natural uranium calls for a very high level of purity, especially with respect to neutron poisons like B, Cd, Gd etc. before it can be used as nuclear fuel. Solvent extraction is a widely used technique by which crude uranium is purified for reactor use. Uranium metal plant (UMP), BARC, Trombay is engaged in refining of uranium concentrate for production of nuclear pure uranium metal for fabrication of fuel for research reactors. This paper reviews some of the fundamental aspects of this refining process with some special references to UMP, BARC. (author)

Laboratory studies on natural restoration of ground water after in-situ leach uranium mining

International Nuclear Information System (INIS)

Bell, N.E.; Deutsch, W.J.; Serne, R.J.

1983-05-01

When uranium is mined using in-situ leach techniques, the chemical quality of the ground water in the ore-zone aquifer is affected. This could lead to long-term degradation of the ground water if restoration techniques are not applied after the leaching is completed. Pacific Northwest Laboratory (PNL), is conducting an NRC-sponsored research project on natural restoration and induced-restoration techniques. Laboratory studies were designed to evaluate the ability of the natural system (ore-zone sediments and groundwater) to mitigate the effects of mining on aquifer chemistry. Using batch and flow-through column experiments [performed with lixiviant (leaching solution) and sediments from the reduced zone of an ore-zone aquifer], we found that the natural system can lower uranium and bicarbonate concentrations in solutions and reduce the lixiviant redox potential (Eh). The change in redox potential could cause some of the contaminants that were dissolved during the uranium leaching operation to precipitate, thereby lowering their solution concentration. The concentrations of other species such as calcium, potassium, and sulfate increased, possibly as a result of mineral dissolution and ion exchange. In this paper, we describe the experimentally determined mobility of contaminants after in-situ leach mining, and discuss the possible chemical process affecting mobility

Laboratory studies on natural restoration of ground water after in-situ leach uranium mining

Energy Technology Data Exchange (ETDEWEB)

Bell, N.E.; Deutsch, W.J.; Serne, R.J.

1983-05-01

When uranium is mined using in-situ leach techniques, the chemical quality of the ground water in the ore-zone aquifer is affected. This could lead to long-term degradation of the ground water if restoration techniques are not applied after the leaching is completed. Pacific Northwest Laboratory (PNL), is conducting an NRC-sponsored research project on natural restoration and induced-restoration techniques. Laboratory studies were designed to evaluate the ability of the natural system (ore-zone sediments and groundwater) to mitigate the effects of mining on aquifer chemistry. Using batch and flow-through column experiments (performed with lixiviant (leaching solution) and sediments from the reduced zone of an ore-zone aquifer), we found that the natural system can lower uranium and bicarbonate concentrations in solutions and reduce the lixiviant redox potential (Eh). The change in redox potential could cause some of the contaminants that were dissolved during the uranium leaching operation to precipitate, thereby lowering their solution concentration. The concentrations of other species such as calcium, potassium, and sulfate increased, possibly as a result of mineral dissolution and ion exchange. In this paper, we describe the experimentally determined mobility of contaminants after in-situ leach mining, and discuss the possible chemical process affecting mobility.

49 CFR 173.426 - Excepted packages for articles containing natural uranium or thorium.

Science.gov (United States)

2010-10-01

... outer surface of the uranium or thorium is enclosed in an inactive sheath made of metal or other durable... uranium or thorium. 173.426 Section 173.426 Transportation Other Regulations Relating to Transportation....426 Excepted packages for articles containing natural uranium or thorium. A manufactured article in...

Validation of gamma-ray detection techniques for safeguards monitoring at natural uranium conversion facilities

Energy Technology Data Exchange (ETDEWEB)

Dewji, S.A., E-mail: dewjisa@ornl.gov [Oak Ridge National Laboratory, 1 Bethel Valley Road, MS-6335, Oak Ridge, TN 37831-6335 (United States); Lee, D.L.; Croft, S. [Oak Ridge National Laboratory, 1 Bethel Valley Road, MS-6335, Oak Ridge, TN 37831-6335 (United States); Hertel, N.E. [Oak Ridge National Laboratory, 1 Bethel Valley Road, MS-6335, Oak Ridge, TN 37831-6335 (United States); Nuclear and Radiological Engineering Program, Georgia Institute of Technology, 770 State Street, Atlanta, GA 30332-0745 (United States); Chapman, J.A.; McElroy, R.D.; Cleveland, S. [Oak Ridge National Laboratory, 1 Bethel Valley Road, MS-6335, Oak Ridge, TN 37831-6335 (United States)

2016-07-01

Recent IAEA circulars and policy papers have sought to implement safeguards when any purified aqueous uranium solution or uranium oxides suitable for isotopic enrichment or fuel fabrication exists. Under the revised policy, IAEA Policy Paper 18, the starting point for nuclear material under safeguards was reinterpreted, suggesting that purified uranium compounds should be subject to safeguards procedures no later than the first point in the conversion process. In response to this technical need, a combination of simulation models and experimental measurements were employed to develop and validate concepts of nondestructive assay monitoring systems in a natural uranium conversion plant (NUCP). In particular, uranyl nitrate (UO{sub 2}(NO{sub 3}){sub 2}) solution exiting solvent extraction was identified as a key measurement point (KMP), where gamma-ray spectroscopy was selected as the process monitoring tool. The Uranyl Nitrate Calibration Loop Equipment (UNCLE) facility at Oak Ridge National Laboratory was employed to simulate the full-scale operating conditions of a purified uranium-bearing aqueous stream exiting the solvent extraction process in an NUCP. Nondestructive assay techniques using gamma-ray spectroscopy were evaluated to determine their viability as a technical means for drawing safeguards conclusions at NUCPs, and if the IAEA detection requirements of 1 significant quantity (SQ) can be met in a timely way. This work investigated gamma-ray signatures of uranyl nitrate circulating in the UNCLE facility and evaluated various gamma-ray detector sensitivities to uranyl nitrate. These detector validation activities include assessing detector responses to the uranyl nitrate gamma-ray signatures for spectrometers based on sodium iodide, lanthanum bromide, and high-purity germanium detectors. The results of measurements under static and dynamic operating conditions at concentrations ranging from 10–90 g U/L of natural uranyl nitrate are presented. A range of

PROCESSING OF URANIUM-METAL-CONTAINING FUEL ELEMENTS

Science.gov (United States)

Moore, R.H.

1962-10-01

A process is given for recovering uranium from neutronbombarded uranium- aluminum alloys. The alloy is dissolved in an aluminum halide--alkali metal halide mixture in which the halide is a mixture of chloride and bromide, the aluminum halide is present in about stoichiometric quantity as to uranium and fission products and the alkali metal halide in a predominant quantity; the uranium- and electropositive fission-products-containing salt phase is separated from the electronegative-containing metal phase; more aluminum halide is added to the salt phase to obtain equimolarity as to the alkali metal halide; adding an excess of aluminum metal whereby uranium metal is formed and alloyed with the excess aluminum; and separating the uranium-aluminum alloy from the fission- productscontaining salt phase. (AEC)

Oxidation of naturally reduced uranium in aquifer sediments by dissolved oxygen and its potential significance to uranium plume persistence

Science.gov (United States)

Davis, J. A.; Smith, R. L.; Bohlke, J. K.; Jemison, N.; Xiang, H.; Repert, D. A.; Yuan, X.; Williams, K. H.

2015-12-01

The occurrence of naturally reduced zones is common in alluvial aquifers in the western U.S.A. due to the burial of woody debris in flood plains. Such reduced zones are usually heterogeneously dispersed in these aquifers and characterized by high concentrations of organic carbon, reduced mineral phases, and reduced forms of metals, including uranium(IV). The persistence of high concentrations of dissolved uranium(VI) at uranium-contaminated aquifers on the Colorado Plateau has been attributed to slow oxidation of insoluble uranium(IV) mineral phases found in association with these reducing zones, although there is little understanding of the relative importance of various potential oxidants. Four field experiments were conducted within an alluvial aquifer adjacent to the Colorado River near Rifle, CO, wherein groundwater associated with the naturally reduced zones was pumped into a gas-impermeable tank, mixed with a conservative tracer (Br-), bubbled with a gas phase composed of 97% O2 and 3% CO2, and then returned to the subsurface in the same well from which it was withdrawn. Within minutes of re-injection of the oxygenated groundwater, dissolved uranium(VI) concentrations increased from less than 1 μM to greater than 2.5 μM, demonstrating that oxygen can be an important oxidant for uranium in such field systems if supplied to the naturally reduced zones. Dissolved Fe(II) concentrations decreased to the detection limit, but increases in sulfate could not be detected due to high background concentrations. Changes in nitrogen species concentrations were variable. The results contrast with other laboratory and field results in which oxygen was introduced to systems containing high concentrations of mackinawite (FeS), rather than the more crystalline iron sulfides found in aged, naturally reduced zones. The flux of oxygen to the naturally reduced zones in the alluvial aquifers occurs mainly through interactions between groundwater and gas phases at the water table

Photochemical process of laboratory uranium wastes recovery

International Nuclear Information System (INIS)

Borges, O.N.; Barros, M.P. de.

1984-01-01

A method for uranium extraction in presence of various aquometallic ions, based on selective photo-reduction of uranium is studied. Some economical advantages in relation with others conventional processes are analysed. (M.J.C.) [pt

Examination of uranium recovery technique from sea water using natural components for adsorbent

International Nuclear Information System (INIS)

Tanaka, Nobuyuki; Masaki, Hiroyuki; Shimizu, Takao; Tokiwai, Moriyasu

2010-01-01

In this study, we investigated the potency of natural components as adsorbent for uranium recovery from seawater. In addition, cost evaluation of uranium recovery from seawater using natural components for adsorbents was performed. Furthermore, new ideas on reservation system of adsorbents at sea area were proposed. Several poly-phenols were selected as adsorbent reagents, then they were adsorbed on the support such as cotton fiber by several methods as the followings; chemical syntheses, electrical beam irradiation, and traditional dyeing. As a result, the adsorbent made by traditional dyeing method using gallnut tannin as natural component, was showed high performance for uranium recovery from seawater on only the first. It was evaluated that traditional dyeing method had also advantage in the manufacturing cost, comparing with earlier method. Additionally, it was considered that reservation system of adsorbent at sea was able to be simplified compared with earlier system. Consequently, uranium recovery from sea water using natural components as adsorbent proposed in this study had a potency of practical use. (author)

Aftermath of Uranium Ore Processing on Floodplains: Lasting Effects of Uranium on Soil and Microbes

Science.gov (United States)

Tang, H.; Boye, K.; Bargar, J.; Fendorf, S. E.

2016-12-01

A former uranium ore processing site located between the Wind River and the Little Wind River near the city of Riverton, Wyoming, has generated a uranium plume in the groundwater within the floodplain. Uranium is toxic and poses a threat to human health. Thus, controlling and containing the spread of uranium will benefit the human population. The primary source of uranium was removed from the processing site, but a uranium plume still exists in the groundwater. Uranium in its reduced form is relatively insoluble in water and therefore is retained in organic rich, anoxic layers in the subsurface. However, with the aid of microbes uranium becomes soluble in water which could expose people and the environment to this toxin, if it enters the groundwater and ultimately the river. In order to better understand the mechanisms controlling uranium behavior in the floodplains, we examined sediments from three sediment cores (soil surface to aquifer). We determined the soil elemental concentrations and measured microbial activity through the use of several instruments (e.g. Elemental Analyzer, X-ray Fluorescence, MicroResp System). Through the data collected, we aim to obtain a better understanding of how the interaction of geochemical factors and microbial metabolism affect uranium mobility. This knowledge will inform models used to predict uranium behavior in response to land use or climate change in floodplain environments.

Analysis of fuel cycles with natural uranium; Analiza gorivnih ciklusa sa prirodnim uranom

Energy Technology Data Exchange (ETDEWEB)

Stojanovic, A [Institute of Nuclear Sciences Boris Kidric, Vinca, Beograd (Yugoslavia)

1965-05-15

A method was developed and a computer code was written for analysis of fuel cycles and it was applied for heavy water and graphite moderated power reactors. Among a variety of possibilities, three methods which enable best utilization of natural uranium and plutonium production were analyzed. Analysis has shown that reprocessing of irradiated uranium and plutonium utilization in the same or similar type of reactor could increase significantly utilization of natural uranium. Increase of burnup is limited exclusively by costs of reprocessing, plutonium extraction and fabrication of new fuel elements.

Migration of uranium daughter radionuclides in natural sediments

International Nuclear Information System (INIS)

Colley, S.; Thomson, J.

1991-01-01

An irregular concentration/depth profile of uranium in deep-sea turbidities, previously elucidated, has been exploited to obtain in-situ effective diffusion coefficients for the long-lived members of the 238 U natural series. The findings are relevant to the assessment of deep-sea sediments as potential repositories for high-level radioactive waste, because waste actinides decay through the same chains of daughter radionuclides as natural actinides. This work was part of the CEC Mirage project-Second phase, Natural analogues research area

Developments in natural uranium - graphite reactors

International Nuclear Information System (INIS)

Bourgeois, J.

1964-01-01

The French natural uranium-graphite power-reactor programme has been developing - from EDF 1 to EDF 4 - in the direction of an increase of the unit power of the installations, of the specific and volume powers, and of an improvement in the operational security conditions. The high power of EDF 4 (500 MWe) and the integration of the primary circuit into the reactor vessel, which is itself made of pre-stressed concrete, make it possible to make the most of the annular fuel elements already in use in EDF 1, and to arrive thus at a very satisfactory solution. The use of an internally cooled fuel element (an annular element) has led to a further step forward: it now becomes possible to increase the pressure of the cooling gas without danger of causing creep in the uranium tube. The use of a pre-stressed concrete vessel makes this pressure increase possible, and the integration of the primary circuit avoids the risk of a rapid depressurization which would be in this case a major danger. This report deals with the main problems presented by this new type of nuclear power station, and gives the main lines of research and studies now being carried out in France. - Neutronic and thermal research has made it possible to consider using large size fuel elements (internal diameter = 77 mm, external diameter 95 mm) while still using natural uranium. - The problems connected with the production of these elements and with their in pile behaviour are the subject of a large programme, both out of pile and in power reactors (EDF 2) and test reactors (Pegase). - The increase in the size of the element leads to a large lattice pitch (35 to 40 cm). This makes it possible to consider having one charging aperture per channel or for a small number of channels, whether the charge machine be inside or outside the pressure vessel. In conclusion are given the main characteristics of a project for a 500 MWe power station using such a fuel element. In particular this project is compared to EDF 4

Improved locations of reactivity devices in future CANDU reactors fuelled with natural uranium or enriched fuels

International Nuclear Information System (INIS)

Boczar, P.G.; Van Dyk, M.T.

1987-02-01

A new configuration of reactivity devices is proposed for future CANDU reactors which improves the core characteristics with enriched fuels, while still allowing the use of natural uranium fuel. Physics calculations for this new configuration are presented for four fuel types: natural uranium, mixed plutonium - uranium oxide (MOX) having a burnup of 21 MWd/kg, and slightly enriched uranium (SEU) having burnups of either 21 or 31 MWd/kg

Bremsstrahlung doses from natural uranium ingots

International Nuclear Information System (INIS)

Anderson, J. L.; Hertel, N. E.

2005-01-01

In the past, some privately owned commercial facilities in the United States were involved in producing or processing radioactive materials used in the production of atomic weapons. Seven different geometrical objects, representative of the configurations of natural uranium metal potentially encountered by workers at these facilities, are modelled to determine gamma ray and Bremsstrahlung dose rates. The dose rates are calculated using the MCNP5 code and also by using the MICROSHIELD point-kernel code. Both gamma ray and Bremsstrahlung dose rates are calculated and combined to obtain a total dose rate. The two methods were found to be in good agreement despite differences in modelling assumptions and method differences. Computed total dose rates on the surface of these objects ranged from ∼51-84 μSv h -1 and 17-95 μSv h -1 using the MCNP5 and the MICROSHIELD modeling, respectively. The partitioning of the computed dose rates between gamma rays and Bremsstrahlung were the same order of magnitude for each object. (authors)

Bremsstrahlung doses from natural uranium ingots.

Science.gov (United States)

Anderson, Jeri L; Hertel, Nolan E

2005-01-01

In the past, some privately owned commercial facilities in the United States were involved in producing or processing radioactive materials used in the production of atomic weapons. Seven different geometrical objects, representative of the configurations of natural uranium metal potentially encountered by workers at these facilities, are modelled to determine gamma ray and bremsstrahlung dose rates. The dose rates are calculated using the MCNP5 code and also by using the MICROSHIELD point-kernel code. Both gamma ray and bremsstrahlung dose rates are calculated and combined to obtain a total dose rate. The two methods were found to be in good agreement despite differences in modelling assumptions and method differences. Computed total dose rates on the surface of these objects ranged from approximately 51-84 microSv h(-1) and 17-95 microSv h(-1) using the MCNP5 and the MICROSHIELD modeling, respectively. The partitioning of the computed dose rates between gamma rays and bremsstrahlung were the same order of magnitude for each object.

Candidate processes for diluting the 235U isotope in weapons-capable highly enriched uranium

International Nuclear Information System (INIS)

Snider, J.D.

1996-02-01

The United States Department of Energy (DOE) is evaluating options for rendering its surplus inventories of highly enriched uranium (HEU) incapable of being used to produce nuclear weapons. Weapons-capable HEU was earlier produced by enriching uranium in the fissile 235 U isotope from its natural occurring 0.71 percent isotopic concentration to at least 20 percent isotopic concentration. Now, by diluting its concentration of the fissile 235 U isotope in a uranium blending process, the weapons capability of HEU can be eliminated in a manner that is reversible only through isotope enrichment, and therefore, highly resistant to proliferation. To the extent that can be economically and technically justified, the down-blended uranium product will be made suitable for use as commercial reactor fuel. Such down-blended uranium product can also be disposed of as waste if chemical or isotopic impurities preclude its use as reactor fuel

Long-term management and use of depleted uranium

International Nuclear Information System (INIS)

Max, A.

2001-01-01

The products resulting from the process of enrichment of natural uranium, or reprocessed uranium, are enriched uranium products as the light fraction and depleted uranium (uranium tails) as the heavy fraction. If the source material is natural uranium, the mass ratios of uranium products and uranium tails can be derived relatively easily from the required enrichment level of the uranium product (product assay (% of U-235)) and the selected depletion level of the uranium tails (tails assay (% of U-235)). The paper discusses among other aspects the dependence of the tails mass on the required enrichment level of the relevant uranium product, for various tails assays. (orig./CB) [de

Correction in the efficiency of uranium purification process by solvent extraction

International Nuclear Information System (INIS)

Franca Junior, J.M.

1981-01-01

An uranium solvent extraction, of high purification, with full advantage of absorbed uranium in the begining of process, is described. Including a pulsed column, called correction column, the efficiency of whole process is increased, dispensing the recycling of uranium losses from leaching column. With the correction column the uranium losses go in continuity, for reextraction column, increasing the efficiency of process. The purified uranium is removed in the reextraction column in aqueous phase. The correction process can be carried out with full efficiency using pulsed columns or chemical mixer-settlers. (M.C.K.) [pt

Process for recovering uranium from wet process phosphoric acid (III)

International Nuclear Information System (INIS)

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

1983-01-01

Uranium is conventionally recovered from wet-process phosphoric acid by two liquid ion exchange steps using a mixture of mono- and disubstituted phenyl esters of orthophosphoric acid (OPPA). Efficiency of the process drops as the mono-OPPA is lost preferentially to the aqueous phase. This invention provides a process for the removal of the uranium process organics (OPPA and organic solvents) from the raffinate of the first liquid ion exchange step and their return to the circuit. The process organics are removed by a combination flotation and absorption step, which results in the recovery of the organics on beads of a hydrophobic styrene polymer

Research on deeply purifying effluent from uranium mining and metallurgy to remove uranium by ion exchange. Pt.2: Elution uranium from lower loaded uranium resin by the intense fractionation process

International Nuclear Information System (INIS)

Zhang Jianguo; Chen Shaoqiang; Qi Jing

2002-01-01

Developing macroporous resin for purifying uranium effluent from uranium mining and metallurgy is presented. The Intense Fractionation Process is employed to elute uranium from lower loaded uranium resin by the eluent of sulfuric acid and ammonium sulfate. The result is indicated that the uranium concentration in the rich elutriant is greatly increased, and the rich liquor is only one bed column volume, uranium concentration in the elutriant is increased two times which concentration is 10.1 g/L. The eluent is saved about 50% compared with the conventional fixed bed elution operation. And also the acidity in the rich elutriant is of benefit to the later precipitation process in uranium recovery

Uranium mineral - groundwater equilibrium at the Palmottu natural analogue study site, Finland

International Nuclear Information System (INIS)

Ahonen, L.; Ruskeeniemi, T.; Blomqvist, R.; Ervanne, H.; Jaakkola, T.

1993-01-01

The redox-potential, pH, chemical composition of fracture waters, and uraninite alteration associated with the Palmottu uranium mineralization (a natural analogue study site for radioactive waste disposal in southwestern Finland), have been studied. The data have been interpreted by means of thermodynamic calculations. The results indicate equilibrium between uraninite, ferric hydroxide and groundwater in the bedrock of the study site. Partially oxidized uraninite (UO 2 .33) and ferric hydroxide are in equilibrium with fresh, slightly acidic and oxidized water type, while primary uraninite is stable with deeper waters that have a higher pH and lower Eh. Measured Eh-pH values of groundwater cluster within a relatively narrow range indicating buffering by heterogenous redox-processes. A good consistency between measured Eh and analyzed uranium oxidation states was observed

Radioactivity and the French uranium bearing minerals

International Nuclear Information System (INIS)

Guiollard, P.Ch.; Boisson, J.M.; Leydet, J.C.; Meisser, N.

1998-01-01

This special issue of Regne Mineral journal is entirely devoted to the French uranium mining industry. It comprises 4 parts dealing with: the uranium mining industry in France (history, uranium rush, deposits, geologic setting, prosperity and recession, situation in 1998, ore processing); radioactivity and the uranium and its descendants (discovery, first French uranium bearing ores, discovery of radioactivity, radium and other uranium descendants, radium mines, uranium mines, atoms, elements and isotopes, uranium genesis, uranium decay, isotopes in an uranium ore, spontaneous fission, selective migration of radionuclides, radon in mines and houses, radioactivity units, radioprotection standards, new standards and controversies, natural and artificial radioactivity, hazards linked with the handling and collecting of uranium ores, conformability with radioprotection standards, radioactivity of natural uranium minerals); the French uranium bearing minerals (composition, crystal structure, reference, etymology, fluorescence). (J.S.)

Problems of natural uranium supply

Energy Technology Data Exchange (ETDEWEB)

Huwyler, S [Eidgenoessisches Inst. fuer Reaktorforschung, Wuerenlingen (Switzerland)

1977-11-01

The estimated uranium reserves in the Western World and the forecast uranium requirement in this region make the supply of nuclear power stations appear guaranteed well beyond the turn of the century. At least in the next decade it will be possible to exploit the advantageous uranium reserves in low price category, provided that prospection activities are stepped up soon and production capacities are expanded in time which are not even fully utilized today. However, difficulties could arise earlier in those countries which have no uranium reserves of their own. There is an increasing tendency among uranium producing countries to link supplies of their uranium with restrictive conditions. This makes long term contractual uranium supply guarantees a most pressing matter for those countries which have no uranium of their own. Even if the delays in the addition of new nuclear power plants are likely to improve the supply situation in the next few years, supply shortages will have to be anticipated at least from the nineties onward, unless exploitation and dressing activities are expanded considerably and also low grade ores are included in the production. At the same time it appears that the use of plutonium fueled fast breeder reactors will be unavoidable in the nineties.

Estimated natural uranium requirements to the year 2000

International Nuclear Information System (INIS)

Bennett, L.L.

1981-01-01

The future requirements for natural uranium are mainly dependent on the future growth of nuclear energy generation and the types of reactors operated to provide that energy. These topics were examined extensively by the International Nuclear Fuel Cycle Evaluation (INFCE). The resulting projections of nuclear power plant capacity and estimated requirements for natural uranium, other nuclear raw materials and fuel cycle services were presented in the final report of INFCE. The projections from INFCE are the most recent results published by an international body, and can therefore be taken as the most authoritative estimates presently available. The INFCE results have been reviewed in the light of latest trends in national nuclear power capacity figures, and a sub-set of the INFCE results are used as the basis for the demand estimates presented in this article. The principal criteria involved in the selection of this sub-set are the nuclear power growth estimates and the reactor and fuel cycle strategies. These criteria are discussed in the following sections

The relationship between natural uranium and advanced fuel cycles in CANDU reactors

International Nuclear Information System (INIS)

Lane, A.D.; McDonnell, F.N.; Griffiths, J.

1988-11-01

CANDU is the most uranium-economic type of thermal power reactor, and is the only type used in Canada. CANDU reactors consume approximately 15% of Canadian uranium production and support a fuel service industry valued at ∼$250 M/a. In addition to their once-through, natural-uranium fuel cycle, CANDU reactors are capable of operating with slightly-enriched uranium (SEU), uranium-plutonium and thorium cycles, more efficiently than other reactors. Only SEU is economically attractive in Canada now, but the other cycles are of interest to countries without indigenous fuel resources. A program is underway to establish the fuel technologies necessary for the use of SEU and the other fuel cycles in CANDU reactors. 22 refs

Content of Natural Radionuclides in Sediments in the Vicinity of a Former Uranium Mine

International Nuclear Information System (INIS)

Strok, M.; Planinsek, P.; Smodis, B.

2011-01-01

Former Slovenian uranium mine Zirovski vrh lies in the subalpine environment with relative high rainfall and population density. As a legacy of uranium mining, Jazbec and Borst waste piles were constructed in the vicinity of a former uranium mine. On the Jazbec waste pile, about 2.5 millions of tons of spoil, and 0.05 millions of tons of red mud were deposited. Average activity concentrations in spoil are 750 Bq/kg for 238U, 226Ra and 230Th, and in red mud 495 Bq/kg for 238U, 190 Bq/kg for 226Ra and 65100 Bq/kg for 230Th. On the Borst waste pile, about 0.6 millions of tons of uranium mill tailings (UMT) were deposited. Average activity concentrations in UMT are 995 Bq/kg for 238U, 8630 Bq/kg for 226Ra and 3930 Bq/kg for 230Th. Seepage waters with elevated radionuclide concentrations from both waste piles flow in the nearby streams Brebovscica and Todrascica. Todrascica outfalls into the Brebovscica and Brebovscica into the Poljanska Sora River. Due to the different biogeochemical processes, natural radionuclides from both waste piles can be transferred to the sediments of the affected streams. These processes are mainly driven by the sorption onto the particles and particles settling or by the direct diffusion to sediments. Therefore the aim of this work was to find out at which extent these processes occur in the specific case by comparing activity concentrations in sediments before and after inflow of seepage waters from both waste piles. In sediment samples, 238U, 234U, 230Th, 226Ra, 210Pb and 210Po activity concentrations were determined, using radiochemical separations followed by either alpha spectrometry or proportional counting. Results of the content of natural radionuclides in sediments in the vicinity of a former uranium mine showed that activity concentrations of all analyzed radionuclides were higher in sediments after the inflow of seepage waters from waste piles in Brebovscica and Todrascica stream. This was not the case for Poljanska Sora River

Treatment of uranium turning with the controllable oxidizing process

International Nuclear Information System (INIS)

Shen Bingyi; Zhang Yonggang; Zhen Huikuan

1989-02-01

The concept, procedure and safety measures of the controllable oxidizing for uranium turning is described. The feasibility study on technological process has been made. The process provided several advantages such as: simplicity of operation, no pollution environment, safety, high efficiency and low energy consumption. The process can yield nuclear pure uranium dioxide under making no use of a great number of chemical reagent. It may supply raw material for fluoration and provide a simply method of treatment for safe store of uranium turning

Process for the in-situ leaching of uranium

International Nuclear Information System (INIS)

Habib, E.T.; Vogt, T.C.

1982-01-01

Process for the in-situ leaching of uranium employing an alkaline lixiviant and an alkali metal or alkaline earth metal hypochlorite as an oxidizing agent. The use of the hypochlorite oxidant results in significantly higher uranium recoveries and leaching rates than those attained by the use of conventional oxidants. The invention is particularly suitable for use in subterranean deposits in which the uranium mineral is associated with carbonaceous material which retards access to the uranium by the lixiviant

Uranium concentrations in natural waters, South Park, Colorado

International Nuclear Information System (INIS)

Sharp, R.R. Jr.; Aamodt, P.L.

1976-08-01

During the summer of 1975, 464 water samples from 149 locations in South Park, Colorado, were taken for the Los Alamos Scientific Laboratory in order to test the field sampling and analytical methodologies proposed for the NURE Hydrogeochemical and Stream Sediment Reconnaissance for uranium in the Rocky Mountain states and Alaska. The study showed, in the South Park area, that the analytical results do not vary significantly between samples which were untreated, filtered and acidified, filtered only, or acidified only. Furthermore, the analytical methods of fluorometry and delayed-neutron counting, as developed at the LASL for the reconnaissance work, provide fast, adequately precise, and complementary procedures for analyzing a broad range of uranium in natural waters. The data generated using this methodology does appear to identify uraniferous areas, and when applied using sound geochemical, geological, and hydrological principles, should prove a valuable tool in reconnaissance surveying to delineate new districts or areas of interest for uranium exploration

Process for recovering uranium from wet process phosphoric acid

International Nuclear Information System (INIS)

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

1982-01-01

A process for recovering uranium from phosphoric acid solutions uses an acidified alkali metal carbonate solution for the second-stage strip of uranyl uranium from the ion-exchange solution. The stripped solution is then recycled to the ion-exchange circuit. In the first stripping stage the ion-exchange solution containing the recovered uranyl uranium and an inert organic diluent is stripped with ammonium carbonate, producing a slurry of ammonium uranyl tricarbonate. The second strip, with a solution of 50-200 grams per litre of sodium carbonate eliminates the problems of inadequate removal of phosphorus, iron and vanadium impurities, solids accumulation, and phase separation in the strip circuit

Internal contamination by natural uranium: monitoring by analysis of urine of individuals exposed by occupational inhalation

International Nuclear Information System (INIS)

Ramalho, A.T.

1982-01-01

Urine samples from men working at Usina Santo Amaro (USAM - State of Sao Paulo), a monazite refinery, were analysed for uranium concentration, using fluorometric analysis and alpha spectrometry. All samples analysed presented uranium concentration below the lower limit of detection. Theoretical values were calculated for uranium concentration in urine samples from workers at the annual limit of intake (ALI) for inhalation of natural uranium, recommended in Publication 30 of the International Commission on Radiological Protection (ICRP, 1979). The two different methods used for analysis of natural uranium concentration in the urine samples were compared: fluorimetry and alpha spectrometry. (author)

Uranium recovery from AVLIS slag

International Nuclear Information System (INIS)

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

2000-01-01

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

Status Report from Czechoslovakia [Processing of Low-Grade Uranium Ores

Energy Technology Data Exchange (ETDEWEB)

Civin, V; Belsky, M [Research and Development Laboratory No.3 of the Uranium Industry, Prague, Czechoslovakia (Czech Republic)

1967-06-15

The present paper deals with the fundamental problems and the main routes followed in processing low-grade uranium ores in CSSR. In this connection it may be useful to discuss the definition of low-grade ore. In our country this term is applied to uraniferous material with a very low content of uranium (of the order of 0.01%) whose treatment causes no particular difficulty. However, the same term is also used to designate those materials whose processibility lies on the verge of economic profitability. In our view, this classification, of an ore using two independent criteria (i.e. uranium content and processing economy) is useful from the standpoint of technology. The treatment of both such ore types is as a rule carried out by specific technological processes. Consequently, low-grade uranium ores can be divided into two groups: (1) Ores with a low uranium content. To this category belong in our country uraniferous materials which originate as a by-product of technological processes used in processing other materials. This is primarily gangue and tailings of various physical or physico-chemical pretreatment operations to which the ore is subjected at the mining site. Mention should be made in this connection of mine waters, which represent a useful complementary source of uranium despite their low uranium content (of the order of milligrams per litre). (2) Ores whose economical treatment is problematic. To this category belong deposits of conventional ore types with a uranium content on the limit of profitable treatment. Also, those deposits containing atypical materials possessing such properties which impair the economy of their treatment. This includes ores with a considerable amount of components which are difficult to separate and which at the same time consume the leaching agents. Finally, it covers uranium-bearing materials in refractory forms which are difficult to dissolve and also some special materials, such as lignites, uranium-bearing shales, loams

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)

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....

The fluorimetry for control of internal contamination of exposed workers to natural and enriched uranium

International Nuclear Information System (INIS)

Gaburo, J.C.; Todo, A.S.; Sordi, G.M.A.A.

2000-01-01

This study is a part of bioassay program revision applied to the uranium processing plants at IPEN-CNEN/SP. The workers of these facilities handle both natural uranium and uranium compounds with different isotopic composition which could reach up to 20% in 235 U. The most commonly employed techniques for the determination of uranium in urine at IPEN are fluorimetry and alpha spectrometry with detection limit of 1.0 mgL-1. and 1,0 mBqL-1 , respectively. Based in advantages and disadvantages of each technique it is very important to identify the workers groups that should be submitted for these analysis. In this report a limiting value of uranium concentration in urine, mgL-1, obtained by fluorimetry is proposed. All the results greater than these limiting value indicate the necessity to carry out a additional measurement by alpha spectroscopy. The uranium mass that result in a pre-determined limit committed effective dose is function of isotopic composition. Consequently, the predicted value of the measured of urinary excretion is function of isotopic composition also and depends of absorption characteristics when inhaled and of the monitoring interval considered. In this report the uranium concentration values for reference levels and limits doses are determined. Based on these results the procedures to use the fluorimetry or both fluorimetry and alpha-spectrometry were adopted. (author)

Uranium tailings sampling manual

International Nuclear Information System (INIS)

Feenstra, S.; Reades, D.W.; Cherry, J.A.; Chambers, D.B.; Case, G.G.; Ibbotson, B.G.

1985-01-01

The purpose of this manual is to describe the requisite sampling procedures for the application of uniform high-quality standards to detailed geotechnical, hydrogeological, geochemical and air quality measurements at Canadian uranium tailings disposal sites. The selection and implementation of applicable sampling procedures for such measurements at uranium tailings disposal sites are complicated by two primary factors. Firstly, the physical and chemical nature of uranium mine tailings and effluent is considerably different from natural soil materials and natural waters. Consequently, many conventional methods for the collection and analysis of natural soils and waters are not directly applicable to tailings. Secondly, there is a wide range in the physical and chemical nature of uranium tailings. The composition of the ore, the milling process, the nature of tailings depositon, and effluent treatment vary considerably and are highly site-specific. Therefore, the definition and implementation of sampling programs for uranium tailings disposal sites require considerable evaluation, and often innovation, to ensure that appropriate sampling and analysis methods are used which provide the flexibility to take into account site-specific considerations. The following chapters describe the objective and scope of a sampling program, preliminary data collection, and the procedures for sampling of tailings solids, surface water and seepage, tailings pore-water, and wind-blown dust and radon

Application of biohydrometallurgy to uranium ore processing

International Nuclear Information System (INIS)

Zhang Jiantang

1989-01-01

The development on application of biohydrometallargy to uranium ore processing is briefly introduced. The device designed for oxidizing ferrous ions in solution by using biomembrane, several bacterial leaching methods and the experimental results are given in this paper. The presented biohydrometallurgical process for recovering uranium includes bacterial leaching following by adsorption using tertiary amine resin 351 and oxidation of ferrous ions in the device with biomembranes. This process brings more economical benefits for treating silicate type original ores. The prospects on application of biogydrometallyurgy to solution mining is also discussed

Uranium Bio-accumulation and Cycling as revealed by Uranium Isotopes in Naturally Reduced Sediments from the Upper Colorado River Basin

Science.gov (United States)

Lefebvre, Pierre; Noël, Vincent; Jemison, Noah; Weaver, Karrie; Bargar, John; Maher, Kate

2016-04-01

Uranium (U) groundwater contamination following oxidized U(VI) releases from weathering of mine tailings is a major concern at numerous sites across the Upper Colorado River Basin (CRB), USA. Uranium(IV)-bearing solids accumulated within naturally reduced zones (NRZs) characterized by elevated organic carbon and iron sulfide compounds. Subsequent re-oxidation of U(IV)solid to U(VI)aqueous then controls the release to groundwater and surface water, resulting in plume persistence and raising public health concerns. Thus, understanding the extent of uranium oxidation and reduction within NRZs is critical for assessing the persistence of the groundwater contamination. In this study, we measured solid-phase uranium isotope fractionation (δ238/235U) of sedimentary core samples from four study sites (Shiprock, NM, Grand Junction, Rifle and Naturita, CO) using a multi-collector inductively coupled plasma mass spectrometer (MC-ICP-MS). We observe a strong correlation between U accumulation and the extent of isotopic fractionation, with Δ238U up to +1.8 ‰ between uranium-enriched and low concentration zones. The enrichment in the heavy isotopes within the NRZs appears to be especially important in the vadose zone, which is subject to variations in water table depth. According to previous studies, this isotopic signature is consistent with biotic reduction processes associated with metal-reducing bacteria. Positive correlations between the amount of iron sulfides and the accumulation of reduced uranium underline the importance of sulfate-reducing conditions for U(IV) retention. Furthermore, the positive fractionation associated with U reduction observed across all sites despite some variations in magnitude due to site characteristics, shows a regional trend across the Colorado River Basin. The maximum extent of 238U enrichment observed in the NRZ proximal to the water table further suggests that the redox cycling of uranium, with net release of U(VI) to the groundwater by

Dietary intake and body content of natural uranium

International Nuclear Information System (INIS)

Anon.

1984-01-01

The members of the uranium series found in the body that arise primarily from dietary intake are 238 U, 234 U, 226 Ra and 210 Pb. Lead 210, the predominant series radionuclide in the body, decays to the alpha emitter 210 Po, while the others are alpha emitters themselves. While 210 Pb primarily enters the body through diet, inhalation must also be considered, especially in smokers. The primary site of deposition for these nuclides is the skeleton and the dose to bone is the critical factor. In this section, the average background, elevated natural and enhanced dietary intakes of the uranium series radionuclides are discussed. Human skeletal levels and consequent alpha doses are summarized

Process for continuous production of metallic uranium and uranium alloys

Science.gov (United States)

Hayden, Jr., Howard W.; Horton, James A.; Elliott, Guy R. B.

1995-01-01

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

Process for continuous production of metallic uranium and uranium alloys

Science.gov (United States)

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

1995-06-06

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

Measurements of natural uranium concentration in Caspian Sea and Persian Gulf water by laser fluorimetric method

International Nuclear Information System (INIS)

Garshasbi, H.; Karimi Diba, J.; Jahanbakhshian, M. H.; Asghari, S. K.; Heravi, G. H.

2005-01-01

Natural uranium exists in earth crust and seawater. The concentration of uranium might increase by human manipulation or geological changes. The aim of this study was to verify susceptibility of laser fluorimetry method to determine the uranium concentration in Caspian Sea and Persian Gulf water. Materials and Methods: Laser fluorimetric method was used to determine the uranium concentration in several samples prepared from Caspian Sea and Persian Gulf water. Biological and chemical substances were eliminated in samples for better evaluation of the method. Results: As the concentration of natural uranium in samples increases, the response of instrument (uranium analyzer) increases accordingly. The standard deviation also increased slightly and gradually. Conclusion: Results indicate that the laser fluorimetry method show a reliable and accurate response with uranium concentration up to 100 μg/L in samples after removal of biological and organic substances

Manual on laboratory testing for uranium ore processing

International Nuclear Information System (INIS)

1990-01-01

Laboratory testing of uranium ores is an essential step in the economic evaluation of uranium occurrences and in the development of a project for the production of uranium concentrates. Although these tests represent only a small proportion of the total cost of a project, their proper planning, execution and interpretation are of crucial importance. The main purposes of this manual are to discuss the objectives of metallurgical laboratory ore testing, to show the specific role of these tests in the development of a project, and to provide practical instructions for performing the tests and for interpreting their results. Guidelines on the design of a metallurgical laboratory, on the equipment required to perform the tests and on laboratory safety are also given. This manual is part of a series of Technical Reports on uranium ore processing being prepared by the IAEA's Division of Nuclear Fuel Cycle and Waste Management. A report on the Significance of Mineralogy in the Development of Flowsheets for Processing Uranium Ores (Technical Reports Series No. 196, 1980) and an instruction manual on Methods for the Estimation of Uranium Ore Reserves (No. 255, 1985) have already been published. 17 refs, 40 figs, 17 tabs

Training manual for uranium mill workers on health protection from uranium

International Nuclear Information System (INIS)

McElroy, N.; Brodsky, A.

1986-01-01

This report provides information for uranium mill workers to help them understand the radiation safety aspects of working with uranium as it is processed from ore to yellowcake at the mills. The report is designed to supplement the radiation safety training provided by uranium mills to their workers. It is written in an easily readable style so that new employees with no previous experience working with uranium or radiation can obtain a basic understanding of the nature of radiation and the particular safety requirements of working with uranium. The report should be helpful to mill operators by providing training material to support their radiation safety training programs

Uranium prospecting program: memorandum of request United Nations Assistance Rotatory Fund for Naturals resources in Uranium Prospecting

International Nuclear Information System (INIS)

1976-01-01

The Uruguayan government required assistance to Unit Nations funds with the aim of studies the Natural resources in Uranium prospecting, their antecedent, actual and projected works, equipment and end considerations

Process for uranium recovery in phosphorus compounds

International Nuclear Information System (INIS)

Demarthe, J.M.; Solar, Serge.

1980-01-01

Process for uranium recovery in phosphorus compounds with an organic phase containing a dialkylphosphoric acid. A solubilizing agent constituted of an heavy alcohol or a phosphoric acid ester or a tertiary phosphine oxide or octanol-2, is added to the organic phase for solubilization of the uranium and ammonium dialkyl pyrophosphate [fr

Geochemical behaviour of natural uranium-series nuclides in geological formation

International Nuclear Information System (INIS)

Yamakawa, Minoru

1991-01-01

Recent research and investigation show that the Tono uranium deposit and its natural uranium-series nuclides have been preserved, without any significant changes like re-migration or reconcentration, throughout geological events such as upheaval-submergence, marine transgression-regression, and faulting which can readily change geological, hydrogeological, and geochemical conditions. This situation might have come about as a result of being kept in a geometrical closure system, with reducing and milk alkalic geochemical conditions, from the hydrogeological and geochemical point of view. (author)

Natural radioactivity around a prospected uranium mining area in Finnish Lapland

International Nuclear Information System (INIS)

Rissanen, K.

1983-01-01

An environmental survey of natural radionuclides was carried out around the Pahtavuoma uranium occurrence site at Kittilae in Finnish Lapland. The aim of the survey was to determine the background levels of these nuclides in the terrestrial and aquatic ecosystems before changing the natural conditions by mining. All of the samples collected were analyzed for Ra-226 after radiochemical separation. Low Ra-226-content, < 0.02 - 1.9 Bg/kg d.w., was measured in locally produced foodstuffs, reindeer, elk and fish, cloudberry and blueberry; levels were 1.4 - 4.6 Bq/kg d.w. in cowberry. Contents of 0.3 - 5 Bq/kg were found in lichen, beard lichen, hay and fish bones, and higher concentrations in elk and reindeer bones (20 - 62 Bq/kg), aquatic plants Hippuris vulgaris (11 - 90 Bq/kg), and sediments (7 - 130 Bq/kg). The highest Ra-226 concentrations (110 - 3100 Bq/kg) were measured in aquatic mosses (Fontinalis sp). The Rn-222 and Ra-226-concentrations measured in surface and well waters were not higher than the average for Finland. Po-210 and Pb-210 determinations are in process. Dose rate and spectroscopic in situ measurements were performed as well. The results indicate lower environmental activity than the average for Lapland, except at the actual uranium mining site

Some economic aspects of natural uranium graphite gas reactor types. Present status and trends of costs in France

International Nuclear Information System (INIS)

Gaussens, J.; Tanguy, P.

1964-01-01

The first part of this report defines the economic advantages of natural uranium fuels, which are as follows: the restricted number and relatively simple fabrication processes of the fuel elements, the low cost per kWh of the finished product and the reasonable capital investments involved in this type of fuel cycle as compared to that of enriched uranium. All these factors combine to reduce the arbitrary nature of cost estimates, which is particularly marked in the case of enriched uranium due to the complexity of its cycle and the uncertainties of plutonium prices). Finally, the wide availability of yellowcake, as opposed to the present day virtual monopoly of isotope separation, and the low cost of natural uranium stockpiling, offer appreciable guarantees in the way of security of supply and economic and political independence as compared with the use of enriched uranium. As far as overall capital investments are concerned, it is shown that, although graphite-gas reactor costs are higher than those of light water reactors in certain capacity ranges, the situation becomes far less clear when we start taking into account, in the interest of national independence, the cost of nuclear fuel production equipment in the case of each of these types of reactor. Finally, the marginal cost of the power capacity of a graphite-gas reactor is low and its technological limitations have receded (owing particularly to the use of prestressed concrete). It is a well known fact that the trend is now towards larger power station units, which means that the rentability of natural uranium graphite reactors as compared to other types of reactors will become more and more pronounced. The second section aims at presenting a realistic short and medium term view of the fuel, running, and investment costs of French natural uranium graphite gas, reactors. Finally, the economic goals which this type of reactor can reach in the very near future are given. It is thus shown that considerable

Uranium resource assessments

International Nuclear Information System (INIS)

1981-01-01

The objective of this investigation is to examine what is generally known about uranium resources, what is subject to conjecture, how well do the explorers themselves understand the occurrence of uranium, and who are the various participants in the exploration process. From this we hope to reach a better understanding of the quality of uranium resource estimates as well as the nature of the exploration process. The underlying questions will remain unanswered. But given an inability to estimate precisely our uranium resources, how much do we really need to know. To answer this latter question, the various Department of Energy needs for uranium resource estimates are examined. This allows consideration of whether or not given the absence of more complete long-term supply data and the associated problems of uranium deliverability for the electric utility industry, we are now threatened with nuclear power plants eventually standing idle due to an unanticipated lack of fuel for their reactors. Obviously this is of some consequence to the government and energy consuming public. The report is organized into four parts. Section I evaluates the uranium resource data base and the various methodologies of resource assessment. Part II describes the manner in which a private company goes about exploring for uranium and the nature of its internal need for resource information. Part III examines the structure of the industry for the purpose of determining the character of the industry with respect to resource development. Part IV arrives at conclusions about the emerging pattern of industrial behavior with respect to uranium supply and the implications this has for coping with national energy issues

Uranium recovery from wet process phosphoric acid

International Nuclear Information System (INIS)

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

1981-01-01

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

ALKALINE CARBONATE LEACHING PROCESS FOR URANIUM EXTRACTION

Science.gov (United States)

Thunaes, A.; Brown, E.A.; Rabbitts, A.T.

1957-11-12

A process for the leaching of uranium from high carbonate ores is presented. According to the process, the ore is leached at a temperature of about 200 deg C and a pressure of about 200 p.s.i.g. with a solution containing alkali carbonate, alkali permanganate, and bicarbonate ion, the bicarbonate ion functionlng to prevent premature formation of alkali hydroxide and consequent precipitation of a diuranate. After the leaching is complete, the uranium present is recovered by precipitation with NaOH.

Thirty years of uranium ore processing in Spain

International Nuclear Information System (INIS)

Josa, J.M.

1982-01-01

Spanish background in the uranium ore processing includes ores from pegmatitic type deposits, vein deposits, sandstone, enrichments in metamorphic rocks, radioactive coals and non-conventional sources of uranium, such as wet phosphoric acid or copper liquors. Some tests have also done in order to recover uranium from very low grade paleozoic quartzites. We have also been involved in by-products recovery (copper) from uranium ores. The technologies that have been used are: physical concentration, combustion and roasting, conventional alkaline or acid methods, pressure, heap and bacteria leaching. Special attention was paid to recover uranium from the pregnant liquors and to develop suited equipment for it; solvent extraction and continuous ion exchange equipment was carefully studied. We have been involved in commercial size (500-3000 t/d) mills, but we have also developed transportable and reussable modular plants specially designed and suited to recover uranium from small and isolated deposits. In both cases the reduction of the environmental impact was taken in account. Spanish experience also includes nuclear purification aspects in order to get uranium nuclear compounds (ADU, UO 2 , UF 4 and UF 6 ). Wet (nitric-TBP) and dry (Fluid-bed) methods have been used. The best of these 30 years of experience in studies and in industrial practice, together with our new developments towards the future, could become in a good contribution for the medium size countries which are going to develop its own uranium industry. The way for these countries could be easier if they know what is valuable and what must be avoid in the uranium ore processing development. In this aim the whole paper was thought and written. (author)

Occupational exposures to uranium: processes, hazards, and regulations

International Nuclear Information System (INIS)

Stoetzel, G.A.; Fisher, D.R.; McCormack, W.D.; Hoenes, G.R.; Marks, S.; Moore, R.H.; Quilici, D.G.; Breitenstein, B.D.

1981-04-01

The United States Uranium Registry (USUR) was formed in 1978 to investigate potential hazards from occupational exposure to uranium and to assess the need for special health-related studies of uranium workers. This report provides a summary of Registry work done to date. The history of the uranium industry is outlined first, and the current commercial uranium industry (mining, milling, conversion, enrichment, and fuel fabrication) is described. This description includes information on basic processes and areas of greatest potential radiological exposure. In addition, inactive commercial facilities and other uranium operations are discussed. Regulation of the commercial production industry for uranium fuel is reported, including the historic development of regulations and the current regulatory agencies and procedures for each phase of the industry. A review of radiological health practices in the industry - facility monitoring, exposure control, exposure evaluation, and record-keeping - is presented. A discussion of the nonradiological hazards of the industry is provided, and the final section describes the tissue program developed as part of the Registry

Uranium concentrations in natural waters, South Park, Colorado. [Part of National Uranium Resource Evaluation program

Energy Technology Data Exchange (ETDEWEB)

Sharp, R.R. Jr.; Aamodt, P.L.

1976-08-01

During the summer of 1975, 464 water samples from 149 locations in South Park, Colorado, were taken for the Los Alamos Scientific Laboratory in order to test the field sampling and analytical methodologies proposed for the NURE Hydrogeochemical and Stream Sediment Reconnaissance for uranium in the Rocky Mountain states and Alaska. The study showed, in the South Park area, that the analytical results do not vary significantly between samples which were untreated, filtered and acidified, filtered only, or acidified only. Furthermore, the analytical methods of fluorometry and delayed-neutron counting, as developed at the LASL for the reconnaissance work, provide fast, adequately precise, and complementary procedures for analyzing a broad range of uranium in natural waters. The data generated using this methodology does appear to identify uraniferous areas, and when applied using sound geochemical, geological, and hydrological principles, should prove a valuable tool in reconnaissance surveying to delineate new districts or areas of interest for uranium exploration.

Behavior of radioactive elements (uranium and thorium) in Bayer process

International Nuclear Information System (INIS)

Sato, C.; Kazama, S.; Sakamoto, A.; Hirayanagi, K.

1986-01-01

It is essential that alumina used for manufacturing electronic devices should contain an extremely low level of alpha-radiation. The principal source of alpha-radiation in alumina is uranium, a minor source being thorium. Uranium in bauxite dissolves into the liquor in the digestion process and is fixed to the red mud as the desilication reaction progresses. A part of uranium remaining in the liquor precipitates together with aluminum hydroxide in the precipitation process. The uranium content of aluminum hydroxide becomes lower as the precipitation velocity per unit surface area of the seed becomes slower. Organic matters in the Bayer liquor has an extremely significant impact on the uranium content of aluminum hydroxide. Aluminum hydroxide free of uranium is obtainable from the liquor that does not contain organic matters

Uranium redistribution under oxidizing conditions in Oklo natural reactor zone 2, Gabon

International Nuclear Information System (INIS)

Isobe, H.; Ohnuki, T.; Murakami, T.; Gauthier-Lafaye, F.

1995-01-01

This mineralogical study was completed to elucidate the relationships between uranium distribution and alteration products of the host rock of natural reactor zone clays just below the reactor core. Uraninite is preserved without any alteration in the reactor core. Uranium minerals are found to be present in the fractures in the reactor zone clays associated with iron-mineral veins, galena and Ti-bearing minerals. Uranium, for which the phases could not be identified, occurs in iron-mineral veins and the iron-mineral rim of pyrite grains in the reactor zone clays. Uranium is not associated with granular iron minerals occurring in the illite matrix of the reactor zone clays. The degree of crystallinity and uranium content of the three iron-bearing alteration products suggest that they formed under different conditions; the granular iron minerals, under alteration conditions where uranium was not mobilized while the iron-mineral veins and the iron-mineral rim of pyrite, under conditions in which uranium is mobilized after the formation of the granular iron minerals

Deep groundwater redox reactions in the Palmottu uranium deposit: The role of uranium and iron in these processes

International Nuclear Information System (INIS)

Bruno, J.; Cera, E.; Duro, L.; Ahonen, L.

1996-12-01

The reduction oxidation properties of the deep bedrock and groundwater are important geochemical factors with respect to the chemical stability of the multibarrier system, which isolates the disposed nuclear fuel from biosphere. In the report are described the results of the redox experiments carried out in the field using the natural groundwaters of Palmottu, in Nummi-Pusula, Finland. The experiments include (1) measurements of natural water redox potential values during four to eight hours continuous pumping; (2) monitoring of the redox-potential response to an artificial change of pH of the groundwater. Separate tests were made in iron and uranium-rich groundwaters, respectively. The data of the field experiments were used in the redox-modelling of the iron and uranium systems. In accordance with earlier knowledge, it was showed that dissolved iron is an important redox electrolyte in natural waters, at least at concentration levels of milligrams per liter. However, a striking observation was that in the absence of dissolved iron dissolved uranium (in concentrations of about 200 nM or more) seems to be able to give nernstian response on platinum electrode in acid/base titrations. The effective redox properties of the bedrock-groundwater system depend on the availability and reactivity of solid phases able to exchange electrons with dissolved redox electrolytes. The present results indicate that, in the bedrock/groundwater system of the Palmottu uranium mineralization, uranium minerals are important redox buffers. (orig.) (refs.)

Linearity assumption in soil-to-plant transfer factors of natural uranium and radium in Helianthus annuus L

International Nuclear Information System (INIS)

Rodriguez, P. Blanco; Tome, F. Vera; Fernandez, M. Perez; Lozano, J.C.

2006-01-01

The linearity assumption of the validation of soil-to-plant transfer factors of natural uranium and 226 Ra was tested using Helianthus annuus L. (sunflower) grown in a hydroponic medium. Transfer of natural uranium and 226 Ra was tested in both the aerial fraction of plants and in the overall seedlings (roots and shoots). The results show that the linearity assumption can be considered valid in the hydroponic growth of sunflowers for the radionuclides studied. The ability of sunflowers to translocate uranium and 226 Ra was also investigated, as well as the feasibility of using sunflower plants to remove uranium and radium from contaminated water, and by extension, their potential for phytoextraction. In this sense, the removal percentages obtained for natural uranium and 226 Ra were 24% and 42%, respectively. Practically all the uranium is accumulated in the roots. However, 86% of the 226 Ra activity concentration in roots was translocated to the aerial part

Linearity assumption in soil-to-plant transfer factors of natural uranium and radium in Helianthus annuus L

Energy Technology Data Exchange (ETDEWEB)

Rodriguez, P. Blanco [Departamento de Fisica, Facultad de Ciencias, Universidad de Extremadura, 06071 Badajoz (Spain); Tome, F. Vera [Departamento de Fisica, Facultad de Ciencias, Universidad de Extremadura, 06071 Badajoz (Spain)]. E-mail: fvt@unex.es; Fernandez, M. Perez [Area de Ecologia, Departamento de Fisica, Facultad de Ciencias, Universidad de Extremadura, 06071 Badajoz (Spain); Lozano, J.C. [Laboratorio de Radiactividad Ambiental, Facultad de Ciencias, Universidad de Salamanca, 37008 Salamanca (Spain)

2006-05-15

The linearity assumption of the validation of soil-to-plant transfer factors of natural uranium and {sup 226}Ra was tested using Helianthus annuus L. (sunflower) grown in a hydroponic medium. Transfer of natural uranium and {sup 226}Ra was tested in both the aerial fraction of plants and in the overall seedlings (roots and shoots). The results show that the linearity assumption can be considered valid in the hydroponic growth of sunflowers for the radionuclides studied. The ability of sunflowers to translocate uranium and {sup 226}Ra was also investigated, as well as the feasibility of using sunflower plants to remove uranium and radium from contaminated water, and by extension, their potential for phytoextraction. In this sense, the removal percentages obtained for natural uranium and {sup 226}Ra were 24% and 42%, respectively. Practically all the uranium is accumulated in the roots. However, 86% of the {sup 226}Ra activity concentration in roots was translocated to the aerial part.

The uranium enrichment industry and the SILEX process

International Nuclear Information System (INIS)

Goldsworthy, M.

1999-01-01

Silex Systems Limited has been developing a new laser isotope separation process since 1992. The principle application of the SILEX Technology is Uranium Enrichment, the key step in the production of fuel for nuclear power plants. The Uranium Enrichment industry, today worth ∼ US$3.5 Billion p.a., is dominated by four major players, the largest being USEC with almost 40% of the market. In 1996, an agreement was signed between Silex and USEC to develop SILEX Technology for potential application to Uranium Enrichment. The SILEX process is a low cost, energy efficient scheme which may provide significant commercial advantage over current technology and competing laser processes. Silex is also investigating possible application to the enrichment of Silicon, Carbon and other materials. Significant markets may develop for such materials, particularly in the semiconductor industry

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.

The progress in the researches for uranium mill tailings cleaning treatment and no-waste uranium ore milling processes

International Nuclear Information System (INIS)

Wang Jintang

1990-01-01

The production of uranium mill tailings and their risk assessment are described. The moethods of uranium mill tailings disposal and management are criticized and the necessity of the researches for uranium mill tailings cleaning treatment and no-wasle uranium ore milling process are demonstrated. The progress for these researches in China and other countries with uranium production is reviewed, and the corresponding conclusions are reported

Test operation of the uranium ore processing pilot plant and uranium conversion plant

International Nuclear Information System (INIS)

Suh, I.S.; Lee, K.I.; Whang, S.T.; Kang, Y.H.; Lee, C.W.; Chu, J.O.; Lee, I.H.; Park, S.C.

1983-01-01

For the guarantee of acid leaching process of the Uranium Ore Processing Pilot Plnat, the KAERI team performed the test operation in coorperation with the COGEMA engineers. The result of the operation was successful achieving the uranium leaching efficiency of 95%. Completing the guarentee test, a continuous test operation was shifted to reconform the reproducibility of the result and check the functions of every units of the pilot plant feeding the low-grade domestic ore, the consistency of the facility was conformed that the uranium can easily be dissolved out form the ore between the temperature range of 60degC-70degC for two hours of leaching with sulfuric acid and could be obtained the leaching efficiency of 92% to 95%. The uranium recovery efficiencies for the processes of extraction and stripping were reached to 99% and 99.6% respectively. As an alternative process for the separation of solid from the ore pulp, four of the Counter Current Decanters were shifted replacing the Belt Filter and those were connected in a series, which were not been tested during the guarantee operation. It was found out that the washing efficiencies of the ore pulp in each tests for the decanters were proportionally increased according to the quantities of the washing water. As a result of the test, it was obtained that washing efficiencies were 95%, 85%, 83% for the water to ore ratio of 3:1, 2:1, 1.5:1 respectively. (Author)

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...

Field technique for the measurement of uranium in natural waters

Energy Technology Data Exchange (ETDEWEB)

Robbins, J C [Scintrex Ltd., Concord, Ontario

1978-05-01

An analytical method suitable for field determination of trace levels of uranium in natural waters is described. Laser UV radiation causes persistent fluorescence of a uranyl complex. Electronic gating substantially rejects detection of short-lived natural organic matter fluorescence. Further work is required on effects of interferences in samples with complex matrices and interpretative aids such as concurrent conductivity and organic content measurements.

Rejuvenation processes applied to 'poisoned' anion exchangers in uranium processing

International Nuclear Information System (INIS)

Gilmore, A.J.

1979-11-01

The removal of 'poisons' from anion exchangers in uranium processing of Canadian radioactive ores is commonly called rejuvenation or regeneration. The cost of the ion exchange recovery of uranium is adversely affected by a decrease in the capacity and efficiency of the anion exchangers, due to their being 'poisoned' by silica, elemental sulphur, molybdenum and tetrathionates. These 'poisons' have a high affinity for the anion exchangers, are adsorbed in preference to the uranyl complex, and do not desorb with the reagents used normally in the uranyl desorption phase. The frequency of rejuvenation and the reagents required for rejuvenation are determined by the severity of the 'poisoning' accumulated by the exchanger in contact with the uranium leach liquor. Caustic soda (NaOH) at approximately equal to 18 cents/lb is commonly used to remove uranium anion exchangers of tetrathionate ((S 4 0 6 )/-/-) 'poisons'. A potential saving in operating cost would be of consequence if other reagents, e.g. sodium carbonate (Na 2 CO 3 ) at approximately equal to 3.6 cents/lb or calcium hydroxide (Ca(OH) 2 ) at approximately equal to 1.9 cents/lb, were effective in removing (S 4 0 6 )/-/-) from a 'poisoned' exchanger. A rejuvenation process for a test program was adopted after a perusal of the literature

Treatment of uranium-containing effluent in the process of metallic uranium parts

International Nuclear Information System (INIS)

Yuan Guoqi

1993-01-01

The anion exchange method used in treatment of uranium-containing effluent in the process of metallic parts is the subject of the paper. The results of the experiments shows that the uranium concentration in created water remains is less than 10 μg/l when the waste water flowed through 10000 column volume. A small facility with column volume 150 litre was installed and 1500 m 3 of waste water can be cleaned per year. (1 tab.)

Alpha spectrometric characterization of process-related particle size distributions from active particle sampling at the Los Alamos National Laboratory uranium foundry

Energy Technology Data Exchange (ETDEWEB)

Plionis, Alexander A [Los Alamos National Laboratory; Peterson, Dominic S [Los Alamos National Laboratory; Tandon, Lav [Los Alamos National Laboratory; Lamont, Stephen P [Los Alamos National Laboratory

2009-01-01

Uranium particles within the respirable size range pose a significant hazard to the health and safety of workers. Significant differences in the deposition and incorporation patterns of aerosols within the respirable range can be identified and integrated into sophisticated health physics models. Data characterizing the uranium particle size distribution resulting from specific foundry-related processes are needed. Using personal air sampling cascade impactors, particles collected from several foundry processes were sorted by activity median aerodynamic diameter onto various Marple substrates. After an initial gravimetric assessment of each impactor stage, the substrates were analyzed by alpha spectrometry to determine the uranium content of each stage. Alpha spectrometry provides rapid nondestructive isotopic data that can distinguish process uranium from natural sources and the degree of uranium contribution to the total accumulated particle load. In addition, the particle size bins utilized by the impactors provide adequate resolution to determine if a process particle size distribution is: lognormal, bimodal, or trimodal. Data on process uranium particle size values and distributions facilitate the development of more sophisticated and accurate models for internal dosimetry, resulting in an improved understanding of foundry worker health and safety.

Initial process development for uranium bioprecipitation

International Nuclear Information System (INIS)

Truex, M.; Peyton, B.; Gorby, Y.; Valentine, N.

1994-01-01

Some bacteria can destabilize soluble metal complexes by enzymatically reducing the metal to a valence state where insoluble compounds are formed. For instance, oxidized uranium (VI) is highly soluble, but it precipitates from solution as the U(IV) oxide uraninite after microbial reduction. The advantage of this technology is that the uranium is easily separated from the aqueous phase, resulting in a small volume of relatively pure uraninite waste. A dissimilatory iron-reducing bacterium capable of uranium reduction was found to have a maximum growth rate of 0.142/hr, a Monod half-saturation constant of 3.4 mg/L, and a cellular yield of 0.071 mg-biomass/mg-iron for iron reduction at 30 C and pH 6.8. The kinetics of iron reduction were used to predict the performance of several reactor configurations for reduction of metals of interest such as uranium. A stirred-tank reactor in series with a plug-flow reactor was determined to be the best configuration for application of the bioprecipitation technology in a continuous-flow process

Temperature Dependence of Uranium and Vanadium Adsorption on Amidoxime-Based Adsorbents in Natural Seawater

Energy Technology Data Exchange (ETDEWEB)

Kuo, Li-Jung [Marine Sciences Laboratory, Pacific Northwest National Laboratory, Sequim WA 98382 USA; Gill, Gary A. [Marine Sciences Laboratory, Pacific Northwest National Laboratory, Sequim WA 98382 USA; Tsouris, Costas [Oak Ridge National Laboratory, Oak Ridge TN 37831 USA; Rao, Linfeng [Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley CA 94720 USA; Pan, Horng-Bin [Department of Chemistry, University of Idaho, Moscow ID 83844 USA; Wai, Chien M. [Department of Chemistry, University of Idaho, Moscow ID 83844 USA; Janke, Christopher J. [Oak Ridge National Laboratory, Oak Ridge TN 37831 USA; Strivens, Jonathan E. [Marine Sciences Laboratory, Pacific Northwest National Laboratory, Sequim WA 98382 USA; Wood, Jordana R. [Marine Sciences Laboratory, Pacific Northwest National Laboratory, Sequim WA 98382 USA; Schlafer, Nicholas [Marine Sciences Laboratory, Pacific Northwest National Laboratory, Sequim WA 98382 USA; D' Alessandro, Evan K. [Rosensteil School of Marine and Atmospheric Chemistry, University of Miami, Miami FL 33149 USA

2018-01-16

The apparent enthalpy and entropy of the complexation of uranium (VI) and vanadium (V) with amidoxime ligands grafted onto polyethylene fiber was determined using time series measurements of adsorption capacities in natural seawater at three different temperatures. The complexation of uranium was highly endothermic, while the complexation of vanadium showed minimal temperature sensitivity. Amidoxime-based polymeric adsorbents exhibit significantly increased uranium adsorption capacities and selectivity in warmer waters.

Studies on uranium ore processing

International Nuclear Information System (INIS)

Suh, I.S.; Chun, J.K.; Park, S.W.; Choi, S.J.; Lee, C.H.; Chung, M.K.; Lim, J.K.

1983-01-01

For the exploitation of domestic uranium ore deposit, comprehensive studies on uranium ore processing of the Geum-San pit ore are carried out. Physical and chemical characteristics of the Geum-San ore are similar to those of Goe-San ore and the physical beneficiation could not be applicable. Optimum operating conditions such as uranium leaching, solid-liquid separation, solvent extraction and precipitation of yellow cake are found out and the results are confirmed by the continous operation of the micro-plant with the capacity of 50Kg, ore/day. In order to improve the process of ore milling pilot plant installed recently, the feasibility of raffinate-recycle and the precipitation methods of yellow cake are intensively examined. It was suggested that the raffinate-recycle in the leaching of filtering stage could be reduced the environmental contamination and the peroxide precipitation technique was applicable to improve the purity of yellow cake. The mechanism and conditions the third phase formation are thoroughly studied and confirmed by chemical analysis of the third phase actually formed during the operation of pilot plant. The major constituents of the third phase are polyanions such as PMosub(12)Osub(40)sup(3-) or SiMosub(12)Osub(40)sup(4-). And the formation of these polyanions could be reduced by the control of redox potential and the addition of modifier. (Author)

Biogeochemical controls of uranium bioavailability from the dissolved phase in natural freshwaters

Science.gov (United States)

Croteau, Marie-Noele; Fuller, Christopher C.; Cain, Daniel J.; Campbell, Kate M.; Aiken, George R.

2016-01-01

To gain insights into the risks associated with uranium (U) mining and processing, we investigated the biogeochemical controls of U bioavailability in the model freshwater speciesLymnaea stagnalis (Gastropoda). Bioavailability of dissolved U(VI) was characterized in controlled laboratory experiments over a range of water hardness, pH, and in the presence of complexing ligands in the form of dissolved natural organic matter (DOM). Results show that dissolved U is bioavailable under all the geochemical conditions tested. Uranium uptake rates follow first order kinetics over a range encompassing most environmental concentrations. Uranium uptake rates in L. stagnalis ultimately demonstrate saturation uptake kinetics when exposure concentrations exceed 100 nM, suggesting uptake via a finite number of carriers or ion channels. The lack of a relationship between U uptake rate constants and Ca uptake rates suggest that U does not exclusively use Ca membrane transporters. In general, U bioavailability decreases with increasing pH, increasing Ca and Mg concentrations, and when DOM is present. Competing ions did not affect U uptake rates. Speciation modeling that includes formation constants for U ternary complexes reveals that the aqueous concentration of dicarbonato U species (UO2(CO3)2–2) best predicts U bioavailability to L. stagnalis, challenging the free-ion activity model postulate.

Uranium recovery from wet-process phosphoric acid

International Nuclear Information System (INIS)

McCullough, J.F.; Phillips, J.F. Jr.; Tate, L.R.

1979-01-01

A method of recovering uranium from wet-process phosphoric acid is claimed where the acid is treated with a mixture of an ammonium salt or ammonia, a reducing agent, and then a miscible solvent. Solids are separated from the phosphoric acid liquid phase. The solid consists of a mixture of metal phosphates and uranium. It is washed free of adhering phosphoric acid with fresh miscible solvent. The solid is dried and dissolved in acid whereupon uranium is recovered from the solution. Miscible solvent and water are distilled away from the phosphoric acid. The distillate is rectified and water discarded. All miscible solvent is recovered for recycle. 5 claims

Simultaneous determination of Ra-226, natural uranium and natural thorium by gamma-ray spectrometry INa(Ti), in solid samples

International Nuclear Information System (INIS)

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

1991-01-01

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

National uranium project - an initiative to generate national database on uranium in drinking water of the country

International Nuclear Information System (INIS)

Sahoo, S.K.; Tripathi, R.M.; Jha, V.N.; Kumar, Ajay; Patra, A.C.; Vinod Kumar, A.

2018-01-01

Uranium is a naturally occurring lithophilic heavy element found in earth crust since inception of the earth. It is present naturally in all rock and soil and the concentration depends on geological formation and local geology. Groundwater interact with the host rocks and the wet weathering process facilitate the solubility of uranium in groundwater. The concentration of uranium in groundwater is influenced by geo-chemical parameters such as host rock characteristics and pH, Eh, ORP, ligands, etc. of the interacting water medium. Uranium is a radioactive element of low specific activity (25 Bq/mg) having both chemical and radiological toxicity but its chemical toxicity supersede the radio-toxicity. After a reporting of high uranium content in drinking water of Punjab, BARC has taken a pro-active initiative to generate a national database on uranium in drinking water in all the districts of India under National Uranium Project (NUP)

Uranium Metal to Oxide Conversion by Air Oxidation –Process Development

Energy Technology Data Exchange (ETDEWEB)

Duncan, A

2001-12-31

Published technical information for the process of metal-to-oxide conversion of uranium components has been reviewed and summarized for the purpose of supporting critical decisions for new processes and facilities for the Y-12 National Security Complex. The science of uranium oxidation under low, intermediate, and high temperature conditions is reviewed. A process and system concept is outlined and process parameters identified for uranium oxide production rates. Recommendations for additional investigations to support a conceptual design of a new facility are outlined.

The French natural uranium industry in 1986

International Nuclear Information System (INIS)

Baron, Marcel

1987-01-01

France has relatively large uranium deposits. This led to the creation of an internationally significant uranium mining industry. The structure of this industry is explained. In 1985 world supply of uranium was greater than world demand leading to an increase in uranium stocks. However, as demand is expected to increase, the industry is undertaking extensive uranium exploration, mainly abroad. (UK)

Isotopic ratio method for determining uranium contamination

International Nuclear Information System (INIS)

Miles, R.E.; Sieben, A.K.

1994-01-01

The presence of high concentrations of uranium in the subsurface can be attributed either to contamination from uranium processing activities or to naturally occurring uranium. A mathematical method has been employed to evaluate the isotope ratios from subsurface soils at the Rocky Flats Nuclear Weapons Plant (RFP) and demonstrates conclusively that the soil contains uranium from a natural source and has not been contaminated with enriched uranium resulting from RFP releases. This paper describes the method used in this determination which has widespread application in site characterizations and can be adapted to other radioisotopes used in manufacturing industries. The determination of radioisotope source can lead to a reduction of the remediation effort

The theory and uses of natural uranium isotopic variations in hydrology

International Nuclear Information System (INIS)

Osmond, J.K.; Cowart, J.B.

1976-01-01

The dissolved concentration of uranium and the relative abundance of two uranium isotopes, 234 U and 238 U, vary over a wide range of values in natural waters. The concentration is controlled mainly by the redox potential of the environment and by CO 2 . The mechanism of isotope fractionation is thought to be entrainment of 234 U in the aqueous phase either by selective leaching of the solid phase or by direct recoil of the daughter nuclide. Ion exchange techniques and alpha-spectrometry permit the measurement of uranium at concentrations as low as pp 10 11 and the isotopic ratio to a few per cent. In oxidizing conditions the uranium isotopes behave in a chemically stable conservative manner such that separate groundwater sources may have identifiably different characteristics and mixing volume calculations may be made. Other potential use of these isotopes include radiometric dating, tracing of hydrologic systems, ore prospecting and earthquake prediction. (author)

Technologies for processing low-grade uranium ores and their relevance to the Indian situation

International Nuclear Information System (INIS)

Murthy, T.K.S.

1991-01-01

The technology for uranium ore processing is well established. Various estimates have shown that on a global basis uranium resources are adequate to meet the forseeable demand. The Indian resources are estimated to be about 60,000 t U. The grade of the ores is low and the individual deposits are small. The nature of the deposits, precarious resources position and relatively small capacity of the mines do not permit the country to take advantage of large throughputs in the mill to achieve substantial cost reduction. However by resorting to as high a scale of milling as the mines would permit, by reducing the loss of solubilised uranium after leaching and by undertaking production of nuclear grade final product at the mill site, significant though not a major, economic benefit can be derived. (author). 2 figs., 3 tabs

Distillation modeling for a uranium refining process

Energy Technology Data Exchange (ETDEWEB)

Westphal, B.R.

1996-03-01

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

Uranium enrichment plans

International Nuclear Information System (INIS)

Thomas, D.C.; Gagne, R.W.

1978-01-01

The following topics are covered: the status of the Government's existing uranium enrichment services contracts, natural uranium requirements based on the latest contract information, uncertainty in predicting natural uranium requirements based on uranium enrichment contracts, and domestic and foreign demand assumed in enrichment planning

Conceptual process design for uranium recovery from sea water

International Nuclear Information System (INIS)

Suzuki, Motoyuki; Chihara, Kazuyuki; Fujimoto, Masahiko; Yagi, Hiroshi; Wada, Akihiko.

1985-01-01

Based on design of uranium recovery process from sea water, total cost for uranium production was estimated. Production scale of 1,000 ton-uranium per year was supposed, because of the big demand for uranium in the second age, i.e., fast breeder reactor age. The process is described as follows: Fluidized bed of hydrous titanium oxide (diameter is 0.1 mm, saturated adsorption capacity is 510 μg-U/g-Ad, adsorption capacity for ten days is 150 μg-U/g-Ad) is supposed, as an example, to be utilized as the primarily concentration unit. Fine adsorbent particles can be transferred as slurry in all of the steps of adsorption, washing, desorption, washing, regeneration. As an example, ammonium carbonate is applied to desorb the adsorbed uranium from titanium oxide. Then, stripping method is adopted for desorbent recovery. As for the secondary concentration, strong basic anion exchange method is supposed. The first step of process design is to determine the mass balance of each component through the whole process system by using the signal diagram. Then, the scale of each unit process, with which the mass balances are satisfied, is estimated by detailed chemical engineering calculation. Also, driving cost of each unit operation is estimated. As a result, minimum total cost of 160,000 yen/kg-U is obtained. Adsorption process cost is 80 to 90 % of the total cost. Capital cost and driving cost are fifty-fifty in the adsorption process cost. Pump driving cost forms a big part of the driving cost. Further concentrated study should be necessary on the adsorption process design. It might be important to make an effort on direct utilization of ocean current for saving the pump driving cost. (author)

Uranium extraction from gold-uranium ores

Energy Technology Data Exchange (ETDEWEB)

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

1981-01-01

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

Analysis of Hazards Associated with a Process Involving Uranium Metal and Uranium Hydride Powders

Energy Technology Data Exchange (ETDEWEB)

Bullock, J.S.

2000-05-01

An analysis of the reaction chemistry and operational factors associated with processing uranium and uranium hydride powders is presented, focusing on a specific operation in the Development Division which was subjected to the Job Hazard Analysis (JHA) process. Primary emphasis is on the thermodynamic factors leading to pyrophoricity in common atmospheres. The discussion covers feed powders, cold-pressed and hot-pressed materials, and stray material resulting from the operations. The sensitivity of the various forms of material to pyrophoricity in common atmospheres is discussed. Operational recommendations for performing the work described are given.

Filtration aids in uranium ore processing

International Nuclear Information System (INIS)

Ford, H.L.; Levine, N.M.; Risdon, A.L.

1975-01-01

The patent describes a process whereby improved flocculation efficiency and filtration of carbonate leached uranium ore pulps are obtained by treating the filter feed slurry with an aqueous solution of hydroxyalkyl guar. (J.R.)

Advanced uranium enrichment processes

International Nuclear Information System (INIS)

Clerc, M.; Plurien, P.

1986-01-01

Three advanced Uranium enrichment processes are dealt with in the report: AVLIS (Atomic Vapour LASER Isotope Separation), MLIS (Molecular LASER Isotope Separation) and PSP (Plasma Separation Process). The description of the physical and technical features of the processes constitutes a major part of the report. If further presents comparisons with existing industrially used enrichment technologies, gives information on actual development programmes and budgets and ends with a chapter on perspectives and conclusions. An extensive bibliography of the relevant open literature is added to the different subjects discussed. The report was drawn up by the nuclear research Centre (CEA) Saclay on behalf of the Commission of the European Communities

Uranium enrichment plans

International Nuclear Information System (INIS)

Gagne, R.W.; Thomas, D.C.

1977-01-01

The status of existing uranium enrichment contracts in the US is reviewed and expected natural uranium requirements for existing domestic uranium enrichment contracts are evaluated. Uncertainty in natural uranium requirements associated with requirements-type and fixed-commitment type contracts is discussed along with implementation of variable tails assay

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

International Nuclear Information System (INIS)

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

1998-01-01

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

Spectroscopic studies of uranium species for environmental decontamination applications

Science.gov (United States)

Eng, Charlotte

After the Cold War, Department of Energy began to concentrate its efforts on cleanup of former nuclear material processing facilities, especially uranium-contaminated groundwater and soil. This research aims to study uranium association to both organic and inorganic compounds found in the contaminated environment in the hopes that the information gathered can be applied to the development and optimization of cost-effective remediation techniques. Spectroscopic and electrochemical methods will be employed to examine the behavior of uranium in given conditions to further our understanding of its impact on the environment. Uranium found in groundwater and soil bind with various ligands, especially organic ligands present in the environment due to natural sources (e.g. metabolic by-products or degradation of plants and animals) or man-made sources (e.g. chelating agents used in operating or cleanup of uranium processing facilities). We selected reasonable analogs of naturally occurring matter and studied their structure, chemical and electrochemical behavior and found that the structure of uranyl complexes depends heavily on the nature of the ligand and environmental factors such as pH. Association of uranium-organic complexes with anaerobic bacteria, Clostridium sp. was studied to establish if the bacteria can effectively bioreduce uranium while going through normal bacterial activity. It was found that the nature of the organic ligand affected the bioavailability and toxicity of the uranium on the bacteria. In addition, we have found that the type of iron corrosion products and uranyl species present on the surface of corroded steel depended on various environmental factors, which subsequently affected the removal rate of uranium by a citric acid/hydrogen peroxide/deionized water cleaning process. The method was found to remove uranium from only the topmost corrosion layers and residual uranium could be found (a) deeper in the corrosion layers where it is occluded by

Distillation modeling for a uranium refining process

International Nuclear Information System (INIS)

Westphal, B.R.

1996-01-01

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

Symposium 'geology, mining and extractive processing of uranium, with special reference to Europe'

International Nuclear Information System (INIS)

Pietsch, H.B.

1977-01-01

This review of the symposium 'Geology, mining and extractive processing of uranium' gives a survey from the point of view of ore processing rather than exploration. A reason for the uranium consumption assumed is given, and uranium deposits and availability, methods of exploration, and interesting facts on uranium extraction from ores are gone into. (HK) [de

Determining factors in the elimination of uranium and radium from groundwaters during a standard potabilization process

Energy Technology Data Exchange (ETDEWEB)

Baeza, A. [Departamento de Fisica, Facultad de Veterinaria, Universidad de Extremadura, Avda. de la Universidad s/n 10071 Caceres (Spain)], E-mail: ymiralle@unex.es; Salas, A. [Departamento de Fisica, Facultad de Veterinaria, Universidad de Extremadura, Avda. de la Universidad s/n 10071 Caceres (Spain); Legarda, F. [Departamento de Ingenieria Nuclear y Mecanica de Fluidos, Escuela Superior de Ingenieros, Universidad de Pais Vasco, Alameda de Urquijo s/n 48013 Bilbao (Spain)

2008-11-15

We studied the physico-chemical and radioactive characteristics of four waters of subsurface origin. They were chosen for having the highest natural radioactivity levels of waters for human consumption in the Autonomous Community of Extremadura, Spain Their activity levels for alpha emitting radionuclides are between 120 and 19 300 mBq L{sup -1}, all exceeding the 100 mBq L{sup -1} threshold established in the European Union above which radioactive isotopes that are present in water should be investigated to determine which corrective action, if any, is needed. These waters were used to compare the efficiency in eliminating their uranium and radium content of two potabilization processes - one the standard chlorination-only process used by their respective municipalities, and the other a procedure consisting of coagulation, flocculation, settling, filtration, and chlorination stages, specifically designed to maximize the elimination of their natural radioactive content. The results showed the uranium and radium elimination efficiencies to depend strongly on the water's hydrogencarbonate, calcium, and magnesium ion concentrations. In particular, with increasing concentrations of any of these ions, the uranium elimination efficiency fell from 90% to 60% at its optimal working pH, pH = 6, while the radium elimination efficiency rose from 50% to 90% at its optimal working pH, pH = 10.

Determining factors in the elimination of uranium and radium from groundwaters during a standard potabilization process.

Science.gov (United States)

Baeza, A; Salas, A; Legarda, F

2008-11-15

We studied the physico-chemical and radioactive characteristics of four waters of subsurface origin. They were chosen for having the highest natural radioactivity levels of waters for human consumption in the Autonomous Community of Extremadura, Spain Their activity levels for alpha emitting radionuclides are between 120 and 19300 mBq L(-1), all exceeding the 100 mBq L(-1) threshold established in the European Union above which radioactive isotopes that are present in water should be investigated to determine which corrective action, if any, is needed. These waters were used to compare the efficiency in eliminating their uranium and radium content of two potabilization processes - one the standard chlorination-only process used by their respective municipalities, and the other a procedure consisting of coagulation, flocculation, settling, filtration, and chlorination stages, specifically designed to maximize the elimination of their natural radioactive content. The results showed the uranium and radium elimination efficiencies to depend strongly on the water's hydrogencarbonate, calcium, and magnesium ion concentrations. In particular, with increasing concentrations of any of these ions, the uranium elimination efficiency fell from 90% to 60% at its optimal working pH, pH=6, while the radium elimination efficiency rose from 50% to 90% at its optimal working pH, pH=10.

Determining factors in the elimination of uranium and radium from groundwaters during a standard potabilization process

International Nuclear Information System (INIS)

Baeza, A.; Salas, A.; Legarda, F.

2008-01-01

We studied the physico-chemical and radioactive characteristics of four waters of subsurface origin. They were chosen for having the highest natural radioactivity levels of waters for human consumption in the Autonomous Community of Extremadura, Spain Their activity levels for alpha emitting radionuclides are between 120 and 19 300 mBq L -1 , all exceeding the 100 mBq L -1 threshold established in the European Union above which radioactive isotopes that are present in water should be investigated to determine which corrective action, if any, is needed. These waters were used to compare the efficiency in eliminating their uranium and radium content of two potabilization processes - one the standard chlorination-only process used by their respective municipalities, and the other a procedure consisting of coagulation, flocculation, settling, filtration, and chlorination stages, specifically designed to maximize the elimination of their natural radioactive content. The results showed the uranium and radium elimination efficiencies to depend strongly on the water's hydrogencarbonate, calcium, and magnesium ion concentrations. In particular, with increasing concentrations of any of these ions, the uranium elimination efficiency fell from 90% to 60% at its optimal working pH, pH = 6, while the radium elimination efficiency rose from 50% to 90% at its optimal working pH, pH = 10

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

International Nuclear Information System (INIS)

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

1996-01-01

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

Modeling of geochemical processes related to uranium mobilization in the groundwater of a uranium mine

International Nuclear Information System (INIS)

Gomez, P.; Garralon, A.; Buil, B.; Turrero, Ma.J.; Sanchez, L.; Cruz, B. de la

2006-01-01

This paper describes the processes leading to uranium distribution in the groundwater of five boreholes near a restored uranium mine (dug in granite), and the environmental impact of restoration work in the discharge area. The groundwater uranium content varied from < 1 μg/L in reduced water far from the area of influence of the uranium ore-containing dyke, to 104 μg/L in a borehole hydraulically connected to the mine. These values, however, fail to reflect a chemical equilibrium between the water and the pure mineral phases. A model for the mobilization of uranium in this groundwater is therefore proposed. This involves the percolation of oxidized waters through the fractured granite, leading to the oxidation of pyrite and arsenopyrite and the precipitation of iron oxyhydroxides. This in turn leads to the dissolution of the primary pitchblende and, subsequently, the release of U(VI) species to the groundwater. These U(VI) species are retained by iron hydroxides. Secondary uranium species are eventually formed as reducing conditions are re-established due to water-rock interactions

Uranium conversion

International Nuclear Information System (INIS)

Oliver, Lena; Peterson, Jenny; Wilhelmsen, Katarina

2006-03-01

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

Recovery of uranium from seawater. 14. System arrangements for the recovery of uranium from seawater by spherical amidoxime chelating resins utilizing natural seawater motions

International Nuclear Information System (INIS)

Egawa, Hiroaki; Kabay, Nalan; Shuto, Taketomi; Jyo, Akinori

1993-01-01

In order to evaluate performances of lightly cross-linked highly porous amidoxime resins in uranium-adsorption systems utilizing natural seawater motions, uranium uptake by the resins from seawater was studied by different approaches, such as simulated sea current exposure tests, towing trials, and/or mooring trials. In general, the efficiency of uranium uptake became higher with a decrease in the thickness of packing layers, indicating important roles of fluidization of the resin particles. On the basis of these fundamental data, mooring tests in the natural sea current were designed and conducted. By mooring flat adsorption beds (base area 260 cm 2 , height 3.0 cm) packed with 780 ml of the resin for 40 h, promising uranium uptake as high as 44 mg/kg of resin (9.9 mg/l of resin) was achieved under sea conditions in which the velocity of sea currents and the vertical velocity of waves were 5.5-49.7 cm/s and 3.4-27 cm/s, respectively

Indian uranium scenario and a new process technology for alkaline leaching

International Nuclear Information System (INIS)

Suri, A.K.; Ghosh, S.K.; Padmanabhan, N.P.H.

2008-01-01

The growing demand of uranium for the nuclear power reactors in the country necessitates maximal utilization of the indigenously available uranium resources. In addition to the single operating uranium mine and the mill at Jaduguda, new mines need to be opened to meet the requirements. However, for the exploitation of the various uranium deposits no single elixir process technology is available and needs to necessarily be developed based on the uranium and gangue mineralogy. One such challenge was development of techno-economic process for exploitation of a reasonably vast deposit at Tummalapalle, Andhra Pradesh. The ore characteristics are much different from that of Jaduguda ore and required alkaline pressure leaching technique to bring the uranium values from the ore into solution. Based on the laboratory and pilot plant studies a working flow sheet has been developed and this paper describes the challenges and how they were tackled. (author)

Development and optimisation of process parameters for recovery of uranium from calcia slag and lining material (SLM) by leaching process and subsequent recovery of uranium from the leach liquor generated

International Nuclear Information System (INIS)

Verma, Dinesh Kumar; Srivastava, Praveen Kumar; Das, Santanu; Kumar, Raj; Roy, S.B.

2014-01-01

Presently uranium value is recovered by nitric acid dissolution of the SLM, to get uranyl nitrate solution (UNS) and subsequent solvent extraction process. UNS generated After SLM dissolution is very lean in uranium content and create difficulty in solvent extraction. Moreover, NO X is also generated during SLM dissolution in nitric acid. An alternate process was developed where nitric acid is not being used and uranium is being recovered by leaching out the SLM using acetic acid. The process was also optimised for recovery and overall economics of the process by using process effluent AALL (Acetic Acid Leach Liquor) as a leaching agent. The uranium value in the leach liquor was precipitated by using sodium hydroxide. The precipitate was dissolved in nitric acid and the Uranyl Nitrate Solution generated was having Uranium concentration of 15-30 g/l. The alternate process developed will have less effluent generation, less NO X generation and will produce more concentrated UNS in comparison to the nitric acid dissolution process

Non-filtration method of processing uranium ores

International Nuclear Information System (INIS)

Laskorin, B.N.; Vodolazov, L.I.; Tokarev, N.N.; Vyalkov, V.I.; Goldobina, V.A.; Gosudarstvennyj Komitet po Ispol'zovaniyu Atomnoj Ehnergii SSSR, Moscow)

1977-01-01

The development of the non-filtration sorption method has lead to procedures of the sorption leaching and the extraction desorption, which have made it possible to intensify the processing of uranium ores and to improve greatly the technical and economic indexes by eliminating the complex method of multiple filtration and re-pulping of cakes. This method makes it possible to involve more poor uranium raw materials, at the same time extracting valuable components such as molybdenum, vanadium, copper, etc. Considerable industrial experience has been acquired in the sorption of dense pulp with a solid-to-liquid phase ratio of 1:1. This has led to a plant production increase of 1.5-3.0 times, an increase of uranium extraction by 5-10%, a two- to- three-fold increase of labour capacity of the main workers, and to a several-fold decrease of reagents, auxiliary materials, electric energy and vapour. This non-filtration method is a continuous process in all its phases thanks to the use of high-yield and high-power equipment for high-density pulps. (author)

PROCESS FOR THE RECOVERY AND PURIFICATION OF URANIUM DEPOSITS

Science.gov (United States)

Carter, J.M.; Kamen, M.D.

1958-10-14

A process is presented for recovering uranium values from UCl/sub 4/ deposits formed on calutrons. Such deposits are removed from the calutron parts by an aqueous wash solution which then contains the uranium values in addition to the following impurities: Ni, Cu, Fe, and Cr. This impurity bearing wash solution is treated with an oxidizing agent, and the oxidized solution is then treated with ammonia in order to precipitate the uranium as ammonium diuranate. The metal impurities of iron and chromium, which form insoluble hydroxides, are precipitated along with the uranium values. The precipitate is separated from the solution, dissolved in acid, and the solution again treated with ammonia and ammonium carbonate, which results in the precipitation of the metal impurities as hydroxides while the uranium values remain in solution.

Status Report from Sweden [Processing of Low-Grade Uranium Ores

Energy Technology Data Exchange (ETDEWEB)

Peterson, A [AB Atomenergi, Stockholm (Sweden)

1967-06-15

The Ministry of Education was authorized in November 1945 to appoint a commission to study the organization of nuclear energy research. In April 1947 this commission, the Swedish Atomic Energy Commission, proposed the formation of a semi-state-owned company to be a central body for applied research work and development in the nuclear energy field in Sweden. In November 1947 the Atomic Energy Company (AB Atomenergi) had its statutory meeting. The State owns 4/7 of the share capital and the remaining 3/7 is owned by 71 private and municipal share-holders. Except for a part of the stock capital, all investments and running costs of the company have been financed by the Government. The company is in practice answerable to the Department of Commerce which has an advisory body, the Atomic Energy Board. AB Atomenergi is responsible for Government-financed research on the industrial applications of nuclear energy, the milling of uranium ores and refining of uranium. The total number of employees is at present about 1400, 800 of which work at the company's research establishment Studsvik about 120 km south of Stockholm. As early as 1945 the Research Institute of the Swedish National Defence started work in the field of uranium processing. Similar work was also started quite early by the Boliden Mining Company, the Swedish Shale Oil Company and Wargons AB. After the establishment of AB Atomenergi, all work in the uranium processing field was transferred to this company. In fact one of the main reasons for the formation of AB Atomenergi was the need for Swedish uranium production as there was no possibility of importing uranium at that time. As a result of research and development in uranium processing a pilot plant at Kvarntorp near Orebro in central Sweden started milling a low-grade uranium ore (shale) in 1953. The capacity of this plant was 5-10 tons of uranium a year. A uranium mill at Ranstad in south-west Sweden, near Skovde, with a capacity of 120 tons of uranium a

Technology of uranium recovery from wet-process phosphoric acid

Energy Technology Data Exchange (ETDEWEB)

Inoue, Katsutoshi [Saga Univ. (Japan). Faculty of Science and Engineering; Nakashio, Fumiyuki

1982-12-01

Rock phosphate contains from 0.005 to 0.02 wt.% of uranium. Though the content is a mere 5 to 10 % of that in uranium ore, the total recovery of uranium is significant since it is used for fertilizer manufacture in a large quantity. Wet-process phosphoric acid is produced by the reaction of rock phosphate with sulfuric acid. The recovery of uranium from this phosphoric acid is mostly by solvent extraction at present. According to U/sup 4 +/ or UO/sub 2//sup 2 +/ as the form of its existence, the technique of solvent extraction differs. The following matters are described: processing of rock phosphate; recovery techniques including the extraction by OPPA-octyl pyrophosphoric acid for U/sup 4 +/, and by mixed DEHPA-Di-(2)-ethylhexyl phosphoric acid and TOPO-tryoctyl phosphine oxide for UO/sub 2//sup 2 +/, and by OPAP-octylphenyl acid phosphate for U/sup 4 +/; the recent progress of the technology as seen in patents.

Uranium price reporting systems

International Nuclear Information System (INIS)

1987-09-01

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

The Palmottu Analogue Project, Progress Report 1993. The behaviour of natural radionuclides in and around uranium deposits, Nr. 7

International Nuclear Information System (INIS)

Ruskeeniemi, T.; Blomqvist, R.; Suksi, J.; Niini, H.

1994-01-01

The report gives a summary of the results of investigations carried out in 1993 at the Palmottu natural analogue study site, which comprises a small U-Th mineralization in Nummi-Pusula, southwestern Finland. Additionally, the report includes several separate articles dealing with various aspects of the Palmottu Analogue Project: (1) 3-dimensional model of fracture zones, (2) redox chemistry of uranium in groundwater, (3) humic substances in groundwater, (4) uranium mineralogy, (5) importance of selective extractions in uranium migration studies, (6) modelling of matrix diffusion, and (7) uranium in surficial deposits. The Palmottu Analogue Project aims at a more profound understanding of radionuclide transport processes in fractured crystalline bedrock. The essential factors controlling transport are groundwater flow and interaction between water and rock. Accordingly, the study includes (1) structural interpretations partly based on geophysical measurements, (2) hydrological studies including hydraulic drill-hole measurements, (3) flow modelling, (4) hydrogeochemical characterization of groundwater, uranium chemistry and colloid chemistry, (5) mineralogical studies, (6) geochemical interpretation and modelling, (7) studies on mobilization and retardation of uranium, and (8) modelling of uranium series data. Paleohydrogeological aspects are of special interest, due to the anticipated future glaciation of the Fennoscandian Shield. Surficial sediments and waters are studied to gain information on postglacial migration in the overburden. (orig.)

The influence on the environment of uranium ore transport from mining sites to processing site in Romania

International Nuclear Information System (INIS)

Peic, T.; Banciu, O.; Bardan, N.; Radulescu, C.

1997-01-01

In Romania, the transport of uranium ores from mining sites to the processing plant is carried out by road and rail. The length of the road transport routes is between 5 and 45 km and rail routes between 300 and 500 km. This laboratory began to monitor these transport routes in 1984. Gamma dose rate measurements were made on and around the special wagons and trucks along the road and rail transport routes and in railway stations. Soil and vegetation samples have also been collected along the road and rail transport routes and in railway stations. From the collected samples the specific activity of natural uranium and 226 Ra were measured. The level of natural radioactivity in the train assembling stations in the period 1984-1996, increased 1-4 times in comparison with the natural background. (Author)

Analysis for the radionuclides of the natural uranium and thorium decay chains with special reference to uranium mine tailings

International Nuclear Information System (INIS)

Lowson, R.T.; Short, S.A.

1986-08-01

A detailed review is made of the experimental techniques that are available, or are in the process of development, for the determination of 238 U, 235 U, 234 U, 231 Pa, 232 Th, 230 Th, 228 Th, 228 Ra, 226 Ra, 223 Ra, 210 Po and 210 Pb. These products of the uranium and thorium decay chains are found in uranium mine tailings. Reference is also made to a procedure for the selective phase extraction of mineral phases from uranium mine tailings

Uranium ore processing in Spain

International Nuclear Information System (INIS)

Josa, J.M.

1976-01-01

The paper presents a review of the Spanish needs of uranium concentrates and uranium ore processing technology and trends in Spain. Spain produces approximately 200t U 3 O 8 /a at two facilities. One plant in the south (Andujar, Jaen) can obtain 70t U 3 O 8 /a and uses a conventional acid leaching process with countercurrent solvent extraction. A second plant, situated in the west (Ciudad Rodrigo, Salamanca) has started in 1975 and has a capacity of 120-130t U 3 O 8 /a, using acid heap leaching and solvent extraction. There is another experimental facility (Don Benito, Badajoz) scheduled to start in 1976 and expected to produce about 25-35t U 3 O 8 /a as a by-product of the research work. For the near future (1978) it is hoped to increase the production with: (a) A new conventional acid leaching/solvent extraction plant in Ciudad Rodrigo; its tentative capacity is fixed at 550t U 3 O 8 /a. (b) A facility in the south, to recover about 130t U 3 O 8 /a from phosphoric acid. (c) Several small mobile plants (30t U 3 O 8 /a per plant); these will be placed near small and isolated mines. The next production increase (1979-1980) will come with the treatment of sandstones (Guadalajara and Cataluna) and lignites(Cataluna); this is being studied. There are also research programmes to study the recovery of uranium from low-grade ores (heap, in-situ and bacterial leaching) and from other industries. (author)

Extraction of uranium from coarse ore and acid-curing and ferric sulphate-trickle leaching process

International Nuclear Information System (INIS)

Jin Suoqing

1994-01-01

On the basis of analysis of the problems in the technology of the traditional uranium hydrometallurgy and the limitations of thin layer leaching process (TLL), a new leaching system-acid-curing and ferric sulphate-trickle leaching (AFL) process (NGJ in Chinese) has developed for extraction of uranium from the coarse ore. The ferric sulphate solution was used for trickling the acid-cured uranium ore and the residual leaching reaction incomplete in TLL process can be improved in this process. And the AFL process has a wide applicability to China's uranium ores, being in competition with the traditional agitation leaching process for treating coarse ores. The uranium ore processing technology based on the AFL process will become one of the new basic technologies of uranium hydrometallurgy. A series of difficulties will be basically overcome associated with fine grinding because of its elimination in the presented process. Moreover, the situation of the present uranium hydrometallurgy can be also changed owing to without technological effluent discharge

Uranium tipped ammunition

International Nuclear Information System (INIS)

Roche, P.

1993-01-01

During the uranium enrichment process required to make nuclear weapons or fuel, the concentration of the 'fissile' U-235 isotope has to be increased. What is left, depleted uranium, is about half as radioactive as natural uranium, but very dense and extremely hard. It is used in armour piercing shells. External radiation levels from depleted uranium (DU) are low. However DU is about as toxic as lead and could be harmful to the kidneys if eaten or inhaled. It is estimated that between 40 and 300 tonnes of depleted uranium were left behind by the Allied armies after the Gulf war. The biggest hazard would be from depleted uranium shells which have hit Iraqui armoured vehicles and the resulting dust inhaled. There is a possible link between depleted uranium shells and an illness known as 'Desert Storm Syndrome' occurring in some Gulf war veterans. As these shells are a toxic and radioactive hazard to health and the environment their use and testing should be stopped because of the risks to troops and those living near test firing ranges. (UK)

Production of annular blanks for Mo-99 using natural uranium, LEU uranium, nickel and structural Al-3003 plates

International Nuclear Information System (INIS)

Lisboa, J.R.; Barrera, M.E.; Marin, J.

2010-01-01

The Tc-99m radioisotope for medical use is the one most used in nuclear medicine worldwide. In Chile the Tc-99m is applied in more than 90% of nuclear medicine studies. In order to supply the whole country with this radioisotope, in 2005-2007 the CCHEN developed its own production of Tc-99m generators from Mo-99 imported from Canada, which are prepared with the activity needed by the Chilean hospitals and clinics. As of 2007 Mo-99 was no longer imported, and since then the Tc-99m is produced only by neutron activation of the Mo. The present challenge is to produce Mo-99 by irradiating blanks that contain enriched uranium foils, with locally produced LEU. The annular blank consists of 2 concentric tubes of A1-3003 structural aluminum that, in an interior annular space, contain a LEU foil, covered on both sides by a nickel foil. This work presents the development of the production technology for annular blanks using natural uranium and U-325 enriched uranium. The structural components are made with A1-3003 aluminum alloy, the foils are 13 grams of uranium measuring 100 x 50 mm and 120-150 μ thick. The blank was assembled using a methodology to control, adapt and assemble the blank's different internal components. A foil of natural uranium and LEU uranium, and a nickel foil are included, used as a barrier for the escape of fission products. During the blank's expansion, for analysis alcohol as lubricant was used, allowing the expander to move smoothly through the inside of the blank. The blank was sealed by TIG welding with a pulsed AC current and a mixture of Ar-5% He gases. Two methods were used for the water tightness test; for high escape levels the temperature was used as a promoter of the ΔP provided by hot water and liquid nitrogen, for low escape levels high vacuum technology was used where the ΔP is provided by a high pressure helium atmosphere. The technology for the production of annular LEU blanks was achieved by applying innovations to technologies

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

International Nuclear Information System (INIS)

1983-01-01

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

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

International Nuclear Information System (INIS)

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

2009-01-01

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

Uranium removal from soils: An overview from the Uranium in Soils Integrated Demonstration program

International Nuclear Information System (INIS)

Francis, C.W.; Brainard, J.R.; York, D.A.; Chaiko, D.J.; Matthern, G.

1994-01-01

An integrated approach to remove uranium from uranium-contaminated soils is being conducted by four of the US Department of Energy national laboratories. In this approach, managed through the Uranium in Soils Integrated Demonstration program at the Fernald Environmental Management Project, Fernald, Ohio, these laboratories are developing processes that selectively remove uranium from soil without seriously degrading the soil's physicochemical characteristics or generating waste that is difficult to manage or dispose of. These processes include traditional uranium extractions that use carbonate as well as some nontraditional extraction techniques that use citric acid and complex organic chelating agents such as naturally occurring microbial siderophores. A bench-scale engineering design for heap leaching; a process that uses carbonate leaching media shows that >90% of the uranium can be removed from the Fernald soils. Other work involves amending soils with cultures of sulfur and ferrous oxidizing microbes or cultures of fungi whose role is to generate mycorrhiza that excrete strong complexers for uranium. Aqueous biphasic extraction, a physical separation technology, is also being evaluated because of its ability to segregate fine particulate, a fundamental requirement for soils containing high levels of silt and clay. Interactions among participating scientists have produced some significant progress not only in evaluating the feasibility of uranium removal but also in understanding some important technical aspects of the task

The Study of Microbial Environmental Processes Related to the Natural Attenuation of Uranium at the Rifle Site using Systems-level Biology

Energy Technology Data Exchange (ETDEWEB)

Methe, Barbara [J. Craig Venter Inst. (JCVI), Rockville, MD (United States); Lipton, Mary [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Mahadevan, Krishna [Univ. of Toronto, ON (Canada)

2016-08-31

Microbes exist in communities in the environment where they are fundamental drivers of global carbon, nutrient and metal cycles. In subsurface environments, they possess significant metabolic potential to affect these global cycles including the transformation of radionuclides. This study examined the influence of microbial communities in sediment zones undergoing biogeochemical cycling of carbon, nutrients and metals including natural attenuation of uranium. This study examined the relationship of both the microbiota (taxonomy) and their metabolic capacity (function) in driving carbon, nutrient and metal cycles including uranium reduction at the Department of Energy (DOE) Rifle Integrated Field Research Challenge (RIFRC). Objectives of this project were: 1) to apply systems-level biology through application of ‘metaomics’ approaches (collective analyses of whole microbial community DNA, RNA and protein) to the study of microbial environmental processes and their relationship to C, N and metals including the influence of microbial communities on uranium contaminant mobility in subsurface settings undergoing natural attenuation, 2) improve methodologies for data generation using metaomics (collectively metagenomics, metatranscriptomics and proteomics) technologies and analysis and interpretation of that data and 3) use the data generated from these studies towards microbial community-scale metabolic modeling. The strategy for examining these subsurface microbial communities was to generate sequence reads from microbial community DNA (metagenomics or whole genome shotgun sequencing (WGS)) and RNA (metatranscriptomcs or RNAseq) and protein information using proteomics. Results were analyzed independently and through computational modeling. Overall, the community model generated information on the microbial community structure that was observed using metaomic approaches at RIFRC sites and thus provides an important framework for continued community modeling

Optimization of dissolution process parameters for uranium ore concentrate powders

Energy Technology Data Exchange (ETDEWEB)

Misra, M.; Reddy, D.M.; Reddy, A.L.V.; Tiwari, S.K.; Venkataswamy, J.; Setty, D.S.; Sheela, S.; Saibaba, N. [Nuclear Fuel Complex, Hyderabad (India)

2013-07-01

Nuclear fuel complex processes Uranium Ore Concentrate (UOC) for producing uranium dioxide powder required for the fabrication of fuel assemblies for Pressurized Heavy Water Reactor (PHWR)s in India. UOC is dissolved in nitric acid and further purified by solvent extraction process for producing nuclear grade UO{sub 2} powder. Dissolution of UOC in nitric acid involves complex nitric oxide based reactions, since it is in the form of Uranium octa oxide (U{sub 3}O{sub 8}) or Uranium Dioxide (UO{sub 2}). The process kinetics of UOC dissolution is largely influenced by parameters like concentration and flow rate of nitric acid, temperature and air flow rate and found to have effect on recovery of nitric oxide as nitric acid. The plant scale dissolution of 2 MT batch in a single reactor is studied and observed excellent recovery of oxides of nitrogen (NO{sub x}) as nitric acid. The dissolution process is automated by PLC based Supervisory Control and Data Acquisition (SCADA) system for accurate control of process parameters and successfully dissolved around 200 Metric Tons of UOC. The paper covers complex chemistry involved in UOC dissolution process and also SCADA system. The solid and liquid reactions were studied along with multiple stoichiometry of nitrous oxide generated. (author)

Process for producing uranium oxide rich compositions from uranium hexafluoride

International Nuclear Information System (INIS)

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

1978-01-01

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

PROCESS OF RECOVERING URANIUM FROM ITS ORES

Science.gov (United States)

Galvanek, P. Jr.

1959-02-24

A process is presented for recovering uranium from its ores. The crushed ore is mixed with 5 to 10% of sulfuric acid and added water to about 5 to 30% of the weight of the ore. This pugged material is cured for 2 to 3 hours at 100 to 110 deg C and then cooled. The cooled mass is nitrate-conditioned by mixing with a solution equivalent to 35 pounds of ammunium nitrate and 300 pounds of water per ton of ore. The resulting pulp containing 70% or more solids is treated by upflow percolation with a 5% solution of tributyl phosphate in kerosene at a rate equivalent to a residence time of about one hour to extract the solubilized uranium. The uranium is recovered from the pregnant organic liquid by counter-current washing with water. The organic extractant may be recycled. The uranium is removed from the water solution by treating with ammonia to precipitate ammonium diuranate. The filtrate from the last step may be recycled for the nitrate-conditioning treatment.

Uranium tetrafluoride production via dioxide by wet process

International Nuclear Information System (INIS)

Aquino, A.R. de.

1988-01-01

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

Evaluation of neutralization treatment processes and their use for uranium tailings solutions

International Nuclear Information System (INIS)

Sherwood, D.R.; Opitz, B.E.; Serne, R.J.

1985-01-01

The potential for groundwater contamination from the typically acidic mill wastes that are disposed of in tailings impoundments is of primary concern at uranium mill sites in the US. Solution-treatment processes provide a system for limiting the environmental impact from acidic seepage. Treatment of uranium tailings solutions from evaporation ponds, underdrains, and surface seeps could aid in decommissioning active sites or be used as an emergency measure to avert possible uncontrolled discharges. At present, neutralization processes appear to be best suited for treating uranium mill tailings solution because they can, at a reasonable cost, limit the solution concentration of many contaminants and thus reduce the potential for groundwater contamination. However, the effectiveness of the neutralization process depends on the reagent used as well as the chemistry of the waste stream. This article provides a description of neutralization processes, an assessment of their performance on acidic uranium tailings leachates, and recommendations for their use at US uranium mill sites

The Palmottu natural analogue project. The behaviour of natural radionuclides in and around uranium deposits. Summary report 1992-1994

International Nuclear Information System (INIS)

Blomqvist, R.; Ruskeeniemi, T.; Ahonen, L.; Suksi, J.; Jakobsson, K.

1995-06-01

The Palmottu U-Th mineralization at Nummi-Pusula, southwestern Finland, has been studied as a natural analogue to deep disposal of radioactive wastes since 1988. The report gives a summary of the results of investigations carried out during the years 1992-1994. The Palmottu Analogue Project aims at a more profound understanding of radionuclide transport processes in fractured crystalline bedrock. The essential factors controlling transport are groundwater flow and interaction between water and rock. Accordingly, the study includes structural interpretations based in part on geophysical measurements, hydrological studies including hydraulic downhole measurements, flow modelling, hydrogeochemical characterization of groundwater, uranium chemistry and colloid chemistry, mineralogical studies, geochemical interpretation and modelling, including paleohydrogeological aspects, and studies of radionuclide mobilization and migration processes including numerical simulations. The project has produced a large amount of data related to natural analogue aspects. The data obtained have already been utilized in developing logical conceptual ideas of the time frames and processes operating in the bedrock of the site. (61 refs., 24 figs., 8 tabs.)

The Palmottu natural analogue project. The behaviour of natural radionuclides in and around uranium deposits. Summary report 1992-1994

Energy Technology Data Exchange (ETDEWEB)

Blomqvist, R; Ruskeeniemi, T; Ahonen, L [Geological Survey of Finland, Espoo (Finland); Suksi, J [Helsinki Univ. (Finland). Lab. of Radiochemistry; Niini, H [Helsinki Univ. of Technology, Otaniemi (Finland). Lab. of Engineering Geology and Geophysics; Vuorinen, U [VTT Chemical Technology, Espoo (Finland); Jakobsson, K [Finnish Centre for Radiation and Nuclear Safety, Helsinki (Finland)

1995-06-01

The Palmottu U-Th mineralization at Nummi-Pusula, southwestern Finland, has been studied as a natural analogue to deep disposal of radioactive wastes since 1988. The report gives a summary of the results of investigations carried out during the years 1992-1994. The Palmottu Analogue Project aims at a more profound understanding of radionuclide transport processes in fractured crystalline bedrock. The essential factors controlling transport are groundwater flow and interaction between water and rock. Accordingly, the study includes structural interpretations based in part on geophysical measurements, hydrological studies including hydraulic downhole measurements, flow modelling, hydrogeochemical characterization of groundwater, uranium chemistry and colloid chemistry, mineralogical studies, geochemical interpretation and modelling, including paleohydrogeological aspects, and studies of radionuclide mobilization and migration processes including numerical simulations. The project has produced a large amount of data related to natural analogue aspects. The data obtained have already been utilized in developing logical conceptual ideas of the time frames and processes operating in the bedrock of the site. (61 refs., 24 figs., 8 tabs.).

Natural uranium equivalent fuel an innovative design for proven CANDU technology

Energy Technology Data Exchange (ETDEWEB)

Pineiro, F.; Ho, K.; Khaial, A.; Boubcher, M.; Cottrell, C.; Kuran, S., E-mail: fabricia.pineiro@candu.com [Candu Energy Inc., Mississauga, ON (Canada); Zhenhua, Z.; Zhiliang, M. [Third Qinshan Nuclear Power Company, Haiyan, Zhejiang (China)

2015-07-01

The high neutron economy, on-power refuelling capability and fuel bundle design simplicity in CANDU reactors allow for the efficient utilization of alternative fuels. Candu Energy Inc. (Candu), in collaboration with the Third Qinshan Nuclear Power Company (TQNPC), the China North Nuclear Fuel Corporation (CNNFC), and the Nuclear Power Institute of China (NPIC), has successfully developed an advanced fuel called Natural Uranium Equivalent (NUE). This innovative design consists of a mixture of recycled and depleted uranium, which can be implemented in existing CANDU stations thereby bringing waste products back into the energy stream, increasing fuel resources diversity and reducing fuel costs. (author)

Natural uranium equivalent fuel. An innovative design for proven CANDU technology

Energy Technology Data Exchange (ETDEWEB)

Pineiro, F.; Ho, K.; Khaial, A.; Boubcher, M.; Cottrell, C.; Kuran, S. [Candu Energy Inc., Mississauga, Ontario (Canada); Zhenhua, Z.; Zhiliang, M. [Third Qinshan Nuclear Power Co., Haiyan, Zhejiang (China)

2015-09-15

The high neutron economy, on-power refuelling capability and fuel bundle design simplicity in CANDU® reactors allow for the efficient utilization of alternative fuels. Candu Energy Inc. (Candu), in collaboration with the Third Qinshan Nuclear Power Company (TQNPC), the China North Nuclear Fuel Corporation (CNNFC), and the Nuclear Power Institute of China (NPIC), has successfully developed an advanced fuel called Natural Uranium Equivalent (NUE). This innovative design consists of a mixture of recycled and depleted uranium, which can be implemented in existing CANDU stations thereby bringing waste products back into the energy stream, increasing fuel resources diversity and reducing fuel costs. (author)

Chapter 3: Exponential experiments on graphite-moderated lattices fuelled with near-natural uranium metal rods

International Nuclear Information System (INIS)

McCulloch, D.B.; Clarke, W.G.; Ashworth, F.P.O.; Hoskins, T.A.

1963-01-01

Exponential experiments have been carried out on graphite lattices fuelled by 1.2 in. diameter uranium metal rods at three near-natural U 235 compositions, 0.6 Co, 1.3 Co and 1.6 Co. The results, together with those already existing from earlier exponential or critical measurements on these and similar natural uranium rods, have been correlated with the theory of Syrett (1961) and also with the modified form of this theory given in Vol.1, Ch. 7. (author)

Remote Handling Devices for Disposition of Enriched Uranium Reactor Fuel Using Melt-Dilute Process

International Nuclear Information System (INIS)

Heckendorn, F.M.

2001-01-01

Remote handling equipment is required to achieve the processing of highly radioactive, post reactor, fuel for the melt-dilute process, which will convert high enrichment uranium fuel elements into lower enrichment forms for subsequent disposal. The melt-dilute process combines highly radioactive enriched uranium fuel elements with deleted uranium and aluminum for inductive melting and inductive stirring steps that produce a stable aluminum/uranium ingot of low enrichment

EPR pilot study on the population of Stepnogorsk city living in the vicinity of a uranium processing plant

Energy Technology Data Exchange (ETDEWEB)

Zhumadilov, Kassym; Akilbekov, Abdirash; Morzabayev, Aidar [L.N. Gumilyov Eurasian National University, Astana (Kazakhstan); Ivannikov, Alexander; Stepanenko, Valeriy [Medical Radiological Research Center, Obninsk (Russian Federation); Abralina, Sholpan; Sadvokasova, Lyazzat; Rakhypbekov, Tolebay [Semey State Medical University, Semey (Kazakhstan); Hoshi, Masaharu [Hiroshima University, Research Institute for Radiation Biology and Medicine, Hiroshima (Japan)

2015-03-15

The aim of this pilot study was to evaluate possible doses in teeth received by workers of a uranium processing plant, in excess to the natural background dose. For this, the electron paramagnetic resonance dosimetry method was applied. Absorbed doses in teeth from the workers were compared with those measured in teeth from the Stepnogorsk city population and a control pool population from Astana city. The measured tooth samples were extracted according to medical indications. In total, 32 tooth enamel samples were analyzed, 5 from Astana city, Kazakhstan (control population), 21 from the residents of Stepnogorsk city (180 km from Astana city), and 6 from the workers of a uranium processing plant. The estimated doses in tooth enamel from the uranium processing plant workers were not significantly different to those measured in enamel from the control population. In teeth from the workers, the maximum dose in excess to background dose was 33 mGy. In two teeth from residents of Stepnogorsk city, however, somewhat larger doses were measured. The results of this pilot study encourage further investigations in an effort to receiving a final conclusion on the exposure situation of the uranium processing plant workers and the residents of Stepnogorsk city. (orig.)

URANIUM SEPARATION PROCESS

Science.gov (United States)

Lyon, W.L.

1962-04-17

A method of separating uranium oxides from PuO/sub 2/, ThO/sub 2/, and other actinide oxides is described. The oxide mixture is suspended in a fused salt melt and a chlorinating agent such as chlorine gas or phosgene is sparged through the suspension. Uranium oxides are selectively chlorinated and dissolve in the melt, which may then be filtered to remove the unchlorinated oxides of the other actinides. (AEC)

Recovery of uranium from crude uranium tetrafluoride

Energy Technology Data Exchange (ETDEWEB)

Ghosh, S K; Bellary, M P; Keni, V S [Chemical Engineering Division, Bhabha Atomic Research Centre, Mumbai (India)

1994-06-01

An innovative process has been developed for recovery of uranium from crude uranium tetrafluoride cake. The process is based on direct dissolution of uranium tetrafluoride in nitric acid in presence of aluminium hydroxide and use of solvent extraction for removal of fluorides and other bulk impurities to make uranium amenable for refining. It is a simple process requiring minimum process step and has advantage of lesser plant corrosion. This process can be applied for processing of uranium tetrafluoride generated from various sources like uranium by-product during thorium recovery from thorium concentrate, first stage product of uranium recovery from phosphoric acid by OPPA process and off grade uranium tetrafluoride material. The paper describes the details of the process developed and demonstrated on bench and pilot scale and its subsequent modification arising out of bulky solid waste generation. The modified process uses a lower quantity of aluminium hydroxide by allowing a lower dissolution of uranium per cycle and recycles the undissolved material to the next cycle, maintaining the overall recovery at high level. This innovation has reduced the solid waste generated by a factor of four at the cost of a slightly larger dissolution vessel and its increased corrosion rate. (author). 4 refs., 1 fig., 3 tabs.

Recovery of uranium from crude uranium tetrafluoride

International Nuclear Information System (INIS)

Ghosh, S.K.; Bellary, M.P.; Keni, V.S.

1994-01-01

An innovative process has been developed for recovery of uranium from crude uranium tetrafluoride cake. The process is based on direct dissolution of uranium tetrafluoride in nitric acid in presence of aluminium hydroxide and use of solvent extraction for removal of fluorides and other bulk impurities to make uranium amenable for refining. It is a simple process requiring minimum process step and has advantage of lesser plant corrosion. This process can be applied for processing of uranium tetrafluoride generated from various sources like uranium by-product during thorium recovery from thorium concentrate, first stage product of uranium recovery from phosphoric acid by OPPA process and off grade uranium tetrafluoride material. The paper describes the details of the process developed and demonstrated on bench and pilot scale and its subsequent modification arising out of bulky solid waste generation. The modified process uses a lower quantity of aluminium hydroxide by allowing a lower dissolution of uranium per cycle and recycles the undissolved material to the next cycle, maintaining the overall recovery at high level. This innovation has reduced the solid waste generated by a factor of four at the cost of a slightly larger dissolution vessel and its increased corrosion rate. (author)

Chemical Separation of Fission Products in Uranium Metal Ingots from Electrolytic Reduction Process

International Nuclear Information System (INIS)

Lee, Chang-Heon; Kim, Min-Jae; Choi, Kwang-Soon; Jee, Kwang-Yong; Kim, Won-Ho

2006-01-01

Chemical characterization of various process materials is required for the optimization of the electrolytic reduction process in which uranium dioxide, a matrix of spent PWR fuels, is electrolytically reduced to uranium metal in a medium of LiCl-Li 2 O molten at 650 .deg. C. In the uranium metal ingots of interest in this study, residual process materials and corrosion products as well as fission products are involved to some extent, which further adds difficulties to the determination of trace fission products. Besides it, direct inductively coupled plasma atomic emission spectrometric (ICP-AES) analysis of uranium bearing materials such as the uranium metal ingots is not possible because a severe spectral interference is found in the intensely complex atomic emission spectra of uranium. Thus an adequate separation procedure for the fission products should be employed prior to their determinations. In present study ion exchange and extraction chromatographic methods were adopted for selective separation of the fission products from residual process materials, corrosion products and uranium matrix. The sorption behaviour of anion and tri-nbutylphosphate (TBP) extraction chromatographic resins for the metals in acidic solutions simulated for the uranium metal ingot solutions was investigated. Then the validity of the separation procedure for its reliability and applicability was evaluated by measuring recoveries of the metals added

Uranium and the War: The effects of depleted uranium weapons in Iraq

International Nuclear Information System (INIS)

Jon williams

2007-01-01

The U.S. Army revealed in March 2003 that it dropped between 320 and 390 tons of depleted uranium during the Gulf War-the first time the material was ever used in combat-and it is estimated that more still has been dropped during the current invasion, though there have been no official counts as yet. Nuclear weapons and nuclear power plants require highly radioactive uranium, so the uranium 238 is removed from the naturally occurring uranium by a process known as enrichment. Depleted uranium is the by-product of the uranium enrichment process. Depleted uranium was a major topic of discussion during a Feb. 24 forum at Santa Cruz with speakers from the Iraq Veterans Against War (IVAW). The panel consisted of five members of the IVAW chapter in Olympia, Washington who visited Santa Cruz as part of a speaking tour of the west coast. These members of the IVAW believe that their experiences in the Gulf War were the beginnings of what will be a long-term health problem in the region. A study conducted by the Pentagon in 2002 predicted that every future battlefield will be contaminated with depleted uranium. Up-to-date health information from Iraq is difficult to come by. But a November report from Al-jazeera concluded that the cancer rate in Iraq has increased tenfold, and the number of birth defects has multiplied fivefold times since the 1991 war. The increase is believed to be caused by depleted uranium.

Method for converting uranium oxides to uranium metal

Science.gov (United States)

Duerksen, Walter K.

1988-01-01

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

Behaviour of organic matters in uranium ore processing

International Nuclear Information System (INIS)

Wu Sanmin

1991-01-01

The oxidation-reduction behaviour of organic matters in the course of oxidation roasting, acid leaching and alkali leaching, the regeneration of humic acid and the consumption of reagents are described. The mineralogical characteristics of the organic matter samples were studied. The results show that its organic matter rich in volatile carbon and with the shorter evolutionary process and lower association is easily oxidized with higher consumption of oxidant during its acid leaching; it is easily oxidized with forming humic acid during alkali leaching; and pretreating it by oxidation roasting is beneficial to the oxidation of uranium. On the contrary, the organic matter rich in fixed carbon, and with longer evolutionary process and higher association is difficultly oxidized with lower consumption of oxidant during its acid leaching; it is difficult to regenerate humic acid for it during alkali leaching; and the uranium can be easily reduced and the leaching performance of uranium can be lowered

Stake holder involvement in the Canadian review process for uranium production projects in Northern Saskatchewan

International Nuclear Information System (INIS)

Underhill, D.

2004-01-01

This report describes the Canadian environmental review process for uranium production projects as a case study for the purpose of understanding the nature and value of stakeholder involvement in the management of radiological hazards. While the Canadian review process potentially applies to any development, this case study focuses on the assessment of the uranium projects of northern Saskatchewan conducted during the 1990's. It describes the environmental assessment (EA) conducted in the 1990's for six new uranium facilities (including mines and mills and related tailings disposal sites) planned in northern Saskatchewan. Both the Canadian federal and the Saskatchewan provincial government have extensive environmental review processes that must under law be complete before any major industrial development judged to have potential environmental impacts is undertaken within their respective territories. However, even in those instances where no clear potential environmental impacts are evident, Canadian law mandates 'if public concern about the proposal is such that a public review is desirable, the initiating department shall refer the proposal to the Minister for review by a Panel'. (Wh95) As a stakeholder under law, in both Canada and Saskatchewan, the public plays an important role in the environmental review process. To encourage participation and assist the public in its review the two governments may provide funding (as done in this review) to assist qualified individuals or groups to participant in the review process. The first section of this case study sets the scene. It describes the Saskatchewan uranium mining story, focusing on how the importance of the public stakeholder evolved to become a major component, under law, in the EA process for new uranium mines. This increase in stakeholder involvement opportunities coincided with heightened public concern for the socio-economic impacts of the projects. In the late 1980's both governments were advised by

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)

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

International Nuclear Information System (INIS)

Zhang Jie; Shen Weiwei; Hao Jidong; Wu Jiangming

2014-01-01

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

Advances in uranium enrichment processes

International Nuclear Information System (INIS)

Rae, H.K.; Melvin, J.G.; Slater, J.B.

1986-05-01

Advances in gas centrifuges and development of the atomic vapour laser isotope separation process promise substantial reductions in the cost of enriched uranium. The resulting reduction in LWR fuel costs could seriously erode the economic advantage of CANDU, and in combination with LWR design improvements, shortened construction times and increased operational reliability could allow the LWR to overtake CANDU. CANDU's traditional advantages of neutron economy and high reliability may no longer be sufficient - this is the challenge. The responses include: combining neutron economy and dollar economy by optimizing CANDU for slightly enriched uranium fuel; developing cost-reducing improvements in design, manufacture and construction; and reducing the cost of heavy water. Technology is a renewable resource which must be continually applied to a product for it to remain competitive in the decades to come. Such innovation is a prerequisite to Canada increasing her share of the international market for nuclear power stations. The higher burn-up achievable with enriched fuel in CANDU can reduce the fuel cycle costs by 20 to 40 percent for a likely range of costs for yellowcake and separative work. Alternatively, some of the benefits of a higher fissile content can take the form of a cheaper reactor core containing fewer fuel channels and less heavy water, and needing only a single fuelling machine. An opportunity that is linked to this need to introduce an enriched uranium fuel cycle into CANDU is to build an enrichment business in Canada. This could offer greater value added to our uranium exports, security of supply for enriched CANDUs, technological growth in Canada and new employment opportunities. AECL has a study in progress to define this opportunity

Analytic study of organic matters in Lodeve uranium ore

International Nuclear Information System (INIS)

Campuzano, E.J.

1981-01-01

Exploitation of uranium in the Permian basin of Lodeve is difficult because of simultaneous extraction of organic matters which are found, in small proportion, in ammonium diuranate and a supplementary purification is required. Available information on natural organic matters are briefly reviewed. Natural organic matters contained in the Lodeve uranium ore processing fluid is separated and fractionated. Physicochemical properties of ligands in each fraction are studied. The existence of bonds between these ligands and dissolved uranium is experimentally demonstrated [fr

Market for natural uranium conversion. Commercial aspect

International Nuclear Information System (INIS)

Durret, L.F.

1986-01-01

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

Radiation protection program applied to occupationally exposed individuals at the IPEN/CNEN-SP pilot plant in the 1980s for natural uranium compounds

International Nuclear Information System (INIS)

Silva, Teresinha de Moraes da; Sordi, Gian Maria A.A.; Vasques, Francisco Mário Feijó

2017-01-01

The work evidences the chemical processing of natural uranium from the yellowcake phase to the production of UF 6 natural uranium hexafluoride, a process carried out at the IPEN/CNEN-SP pilot plant. Radiation protection management was intended to monitor occupationally exposed individuals - IOEs, the workplace and the environment. An individual monitoring program for IOEs was developed for both external irradiation and incorporation of radioactive material. The IOEs were monitored externally with film-type dosimeters and the in vitro method was applied internally for urine analysis. For the workplace the monitoring program for equipment and floors was developed, determining the exposure rate from the process equipment, surface contamination expressed in Bq.cm -2 in equipment and floors, complemented by the air monitoring program both for the worker as well as for the workplace. Cellulose filters with aerodynamic diameter of 0.3 micron to 8.0 micron were used

Uranium recovery from slags of metallic uranium

International Nuclear Information System (INIS)

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

2006-01-01

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

Uranium removal from organic solutions of PUREX process

International Nuclear Information System (INIS)

Dell'Occhio, L.A.; Dupetit, G.A.; Pascale, A.A.; Vicens, H.E.

1987-01-01

During the uranium extraction process with tributyl phosphate (TBP) in nitric medium, a bi solvated, non hydrated complex is formed, of formula UO2(NO3)2TBP, which is soluble in the diluent, a paraffin hydrocarbon. As it is known that some uranium salts, for instance the nitrate, when dissolved in organic solvents, like isopropanol, can be discharged as complex molecules at the cathode of an electrodeposition cell, it was decided to apply this technique to uranium loaded TBP solutions. From preliminary experiments resulted a practical possibility for the analytical control through the alpha measurement of electro deposits. This technique could be applied as well to the treatment of depleted organic streams carrying undesirable alpha activity, because the so treated solutions become deprived of uranium. This work presents the curves obtained working at constant voltage with uranium-loaded TBP solutions, the determination of the optimal operation voltage in these conditions, the electrodeposition yield for electro polished copper and stainless steel cathodes and the tests of reproducibility of deposits. A summary of the results obtained operating the high voltage supply at constant power is also presented. (Author)

Recycling of reprocessed uranium

International Nuclear Information System (INIS)

Randl, R.P.

1987-01-01

Since nuclear power was first exploited in the Federal Republic of Germany, the philosophy underlying the strategy of the nuclear fuel cycle has been to make optimum use of the resource potential of recovered uranium and plutonium within a closed fuel cycle. Apart from the weighty argument of reprocessing being an important step in the treatment and disposal of radioactive wastes, permitting their optimum ecological conditioning after the reprocessing step and subsequent storage underground, another argument that, no doubt, carried weight was the possibility of reducing the demand of power plants for natural uranium. In recent years, strategies of recycling have emerged for reprocessed uranium. If that energy potential, too, is to be exploited by thermal recycling, it is appropriate to choose a slightly different method of recycling from the one for plutonium. While the first generation of reprocessed uranium fuel recycled in the reactor cuts down natural uranium requirement by some 15%, the recycling of a second generation of reprocessed, once more enriched uranium fuel helps only to save a further three per cent of natural uranium. Uranium of the second generation already carries uranium-232 isotope, causing production disturbances, and uranium-236 isotope, causing disturbances of the neutron balance in the reactor, in such amounts as to make further fabrication of uranium fuel elements inexpedient, even after mixing with natural uranium feed. (orig./UA) [de

Contamination of roads in Klatovy by natural radionuclides from waste rock dumps of the former uranium mine Ustalec

International Nuclear Information System (INIS)

Nekl, M.; Golias, V.

2002-01-01

Contamination by natural radioisotopes was detected in the road network of the town Klatovy (Czech Republic). The extent and distribution of the contamination were studied using automobile and portable gamma ray spectrometers. Samples of the roadway were taken for a mineralogical and petrological study at two localities. Processes of re-distribution of uranium in the road and its surroundings were studied. (author)

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

International Nuclear Information System (INIS)

Moraes da Silva, T. de

1990-01-01

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

Determination of natural and depleted uranium in urine at the ppt level: an interlaboratory analytical exercise

International Nuclear Information System (INIS)

D'Agostino, P.A.; Ough, E.A.; Glover, S.E.; Vallerand, A.L.

2002-10-01

An analytical exercise was initiated in order to determine those analytical procedures with the capacity to measure uranium isotope ratios ( 238 U/ 235 U) in urine samples containing less that 1μ uranium /L urine. A host laboratory was tasked with the preparation of six sets (12 samples per set) of synthetic urine samples spiked with varying amounts of natural and depleted (0.2% 235 U) uranium. The sets of samples contained total uranium in the range 25 ng U/L urine to 770 ng U/L urine, with isotope ratios ( 238 U/ 235 U) from 137.9 (natural uranium) to 215 (∼50% depleted uranium). Sets of samples were shipped to five testing laboratories (four Canadian and one European) for total and isotopic assay. The techniques employed in the analyses included sector field inductively coupled plasma mass spectrometry (ICP-SF-MS), quadrupole inductively coupled plasma mass spectrometry (ICP-Q-MS), thermal ionization mass spectrometry (TIMS) and neutron activation analysis (NAA). Full results were obtained from three testing labs (ICP-SF-MS, ICP-Q-MS and TIMS). Their results, plus partial results from the NAA lab, have been included in this report. Total uranium and isotope ratio results obtained from ICP-SF-MS and ICP-Q-MS were in good agreement with the host lab values. Neutron activation analysis and TIMS reported total uranium concentrations that differed from the host lab. An incomplete set of isotopic ratios was obtained from the NAA lab with some results reporting enriched uranium (% 235 U > 0.7). Based on the reported results, the four analytical procedures were ranked: ICP-SF-MS (1), ICP-Q-MS (2), TIMS (3) and NAA (4). (author)

Imprints left by natural radioactivity in geological materials: uranium fission tracks and thermoluminescence applications in earth sciences

International Nuclear Information System (INIS)

Broquet, P.; Chambaudet, A.; Rebetez, M.; Charlet, J.M.

1994-01-01

In a rock, all minerals which contain uranium are host to a number of spontaneous fission phenomena forming a single damaged area called a ''latent track'', observations of which may lead to dating, uranium mapping and finding paleo-geo-thermometers (thermal history, used in oil exploration). The radioactive elements during the decay process release energy which is trapped as electrons into the physical or chemical defects of the crystalline lattice; this energy can be later released by heating the mineral (thermic stimulated luminescence); the thermoluminescence is characterized by a glow which spectrum constitutes a typical feature of the mineral, its crystallization conditions and the subsequent evolution of the material. Natural and induced glow curve may be produced. 6 figs., 52 refs

Analysis and exploitation of bacterial population from natural uranium-rich soils: selection of a model specie

International Nuclear Information System (INIS)

Mondani, L.

2010-01-01

It is well known that soils play a key role in controlling the mobility of toxic metals and this property is greatly influenced by indigenous bacterial communities. This study has been conducted on radioactive and controls soils, collected in natural uraniferous areas (Limousin). A physico-chemical and mineralogical analysis of soils samples was carried out.The structure of bacterial communities was estimated by Denaturing Gradient Gel Electrophoresis (DGGE). The community structure is remarkably more stable in the uranium-rich soils than in the control ones, indicating that uranium exerts a high selection from the soils was constructed and screened for uranium resistance in order to study bacteria-uranium interactions. Scanning electron microscopy revealed that a phylo-genetically diverse set of uranium-resistant species ware able to chelate uranium at the cell surface. (author) [fr

Process of quantity determination of uranium by chromatography in liquid zone

International Nuclear Information System (INIS)

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

1993-01-01

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

Uranium conversion; Urankonvertering

Energy Technology Data Exchange (ETDEWEB)

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

2006-03-15

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

Uranium enrichment plans and policies

International Nuclear Information System (INIS)

Schwennesen, J.L.

1981-01-01

Significant progress has been made in US efforts to expand its enrichment capacity. The Cascade Improvement Program (CIP) and Cascade Upgrading Program (CUP) are now complete at Oak Ridge and Paducah and almost complete at Portsmouth. Considerable progress has also been made in constructing the Gas Centrifuge Enrichment Plant (GCEP), and physical construction of the first process building is well under way. Current plans are to have two process buildings on-line by 1989 with the remaining six buildings to be added sequentially as needed to meet demand. The status of DOE enrichment services contracts is essentially unchanged from that reported at last year's seminar. The OUEA latest forecast of nuclear power growth, however, is considerably lower than reported last year, although a leveling trend is becoming apparent. The Variable Tails Assay Option (VTAO) of the AFC contract was made available for the third time for FY 1983. The DOE inventories of natural uranium still remain high. The Department of Energy will dispose of this material by using it for Government programs and for enrichment plant operations. It appears that Government inventories of uranium are adequate through at least the mid-1990s. It remains DOE policy not to dispose of its natural uranium stocks through direct sales in the marketplace, except for very small quantities or if an emergency situation would exist and all reasonable attempts had been made, without success, to obtain natural uranium from commercial sources. Finally, with regard to DOE plans on future transaction tails assays, it still appears likely that the current 0.20 percent uranium-235 reference tails assay will be maintained until well into the 1990s, at which time it might be increased up to 0.25 percent uranium-235

Contamination with uranium from natural and anthropological sources

International Nuclear Information System (INIS)

Todorov, Peter Todorov; Ilieva, Elica Nikolova

2005-01-01

Our world is radioactive and always was since it was created. Radioactive elements are often called radioactive isotopes or radionuclides. Radionuclides are found in the environment as naturally occurring elements and as products or byproducts of nuclear technologies. One of the most common radionuclides is Uranium (U). U with atomic number of 92 is the heaviest known natural element. All U isotopes are radioactive. So it is very important their quantity to be under control. Natural U is used in the generation of nuclear fuel. U - 235 is one of two fissile materials used for the production of nuclear weapons and in some nuclear reactors as a source of energy. Because of its use in the fission process U is found in large quantities in stored nuclear waste. Other important source of U to the environment was the nuclear weapon tests, especially during the second half of 20th century. Artificial radionuclides may also be released into the environment from non - nuclear cycle activities in industry and research and from usage in diagnostic and therapeutic medicine. Erosion of agricultural soils may input the 238 U decay radionuclides into drinking water supplies in areas with heavy fertilizer usage. The most common routes of U contamination are through handling, ingesting and inhaling. Inhaling and ingesting increase the risk of lung and bone cancer. U is also chemically toxic at high concentrations. U may also affect reproductive organs and the foetus, and may increase the risk of leukemia and soft tissue cancer. (authors)

Process for sewage biological treatment from uranium

International Nuclear Information System (INIS)

Popa, K.; Cecal, A.; Craciun, I.

2004-01-01

The invention relates to the sewage treatment, in particular to the sewage biological treatmen from radioactive waste, namely from uranium. The process dor sewage biological treatment from uranium includes cultivation in the sewage of the aquatic plants Lemna minor and Spirulina platensis. The plants cultivation is carried out in two stages. In the first stage for cultivation is used Lemna minor in the second stage - Spirulina platensis . After finishing the plant cultivation it is carried out separation of their biomass. The result of the invention consists in increasing the uranyl ions by the biomass of plants cultivated in the sewage

Process for sewage biological treatment from uranium

International Nuclear Information System (INIS)

Popa, Karin; Cecal, Alexandru; Craciun, Iftimie Ionel; Rudic, Valeriu; Gulea, Aurelian; Cepoi, Liliana

2004-01-01

The invention relates to the sewage treatment, in particular to the sewage biological treatment from radioactive waste, namely from uranium. The process for sewage biological treatment from uranium includes cultivation in the sewage of the aquatic plants Lemna minor and Spirulina platensis. The plant cultivation is carried out in two stages. In the first stage for cultivation is used Lemna minor and in the second stage - Spirulina platensis. After finishing the plant cultivation it is carried out separation of their biomass. The result of the invention consists in increasing the uranyl ions accumulation by the biomass of plants cultivated in the sewage.

Uranium Enrichment, an overview

International Nuclear Information System (INIS)

Coates, J.H.

1994-01-01

This general presentation on uranium enrichment will be followed by lectures on more specific topics including descriptions of enrichment processes and assessments of the prevailing commercial and industrial situations. I shall therefore avoid as much as possible duplications with these other lectures, and rather dwell on: some theoretical aspects of enrichment in general, underlying the differences between statistical and selective processes, a review and comparison between enrichment processes, remarks of general order regarding applications, the proliferation potential of enrichment. It is noteworthy that enrichment: may occur twice in the LWR fuel cycle: first by enriching natural uranium, second by reenriching uranium recovered from reprocessing, must meet LWR requirements, and in particular higher assays required by high burn up fuel elements, bears on the structure of the entire front part of the fuel cycle, namely in the conversion/reconversion steps only involving UF 6 for the moment. (author). tabs., figs., 4 refs

Development of practical decontamination process for the removal of uranium from gravel.

Science.gov (United States)

Kim, Ilgook; Kim, Gye-Nam; Kim, Seung-Soo; Choi, Jong-Won

2018-01-01

In this study, a practical decontamination process was developed to remove uranium from gravel using a soil washing method. The effects of critical parameters including particle size, H 2 SO 4 concentration, temperature, and reaction time on uranium removal were evaluated. The optimal condition for two-stage washing of gravel was found to be particle size of 1-2 mm, 1.0 M H 2 SO 4 , temperature of 60°C, and reaction time of 3 h, which satisfied the required uranium concentration for self-disposal. Furthermore, most of the extracted uranium was removed from the waste solution by precipitation, implying that the treated solution can be reused as washing solution. These results clearly demonstrated that our proposed process can be indeed a practical technique to decontaminate uranium-polluted gravel.

Improvement for waste water treatment process of a uranium deposite and its effect

International Nuclear Information System (INIS)

Huang Jimao

2013-01-01

Uranium was recovered from alkaline uranium ores by heap leaching and traditional agitation leaching methods at a uranium mine, and the waste water (including waste water produced in hydrometallurgy process and mine drainage) was treated by using chemical precipitation method and chemical precipitation loading method. It was found that the removal rate of uranium by the waste water treatment process was not satisfactory after one year's run. So, the waste water treatment process was improved. After the improvement, removal rate of CO 3 2- ,HCO 3 - , U and Ra was enhanced and the treated waste water reached the standard of discharge. (author)

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

International Nuclear Information System (INIS)

Monteillet, A.

1985-02-01

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

Uranium pollution in an estuary affected by pyrite acid mine drainage and releases of naturally occurring radioactive materials

International Nuclear Information System (INIS)

Villa, M.; Manjon, G.; Hurtado, S.; Garcia-Tenorio, R.

2011-01-01

Highlights: → Huelva estuary is affected by former phosphogypsum releases and pyrite acid mine drainage. → Time evolution of uranium concentration is analyzed after halting of NORM releases. → Two new contamination sources are preventing the complete uranium cleaning: (1) The leaching of phosphogypsum stacks located close to Tinto River. (2) Pyrite acid mine drainage. → High uranium concentrations are dissolved in water and precipitate subsequently. - Abstract: After the termination of phosphogypsum discharges to the Huelva estuary (SW Spain), a unique opportunity was presented to study the response of a contaminated environmental compartment after the cessation of its main source of pollution. The evolution over time of uranium concentrations in the estuary is presented to supply new insights into the decontamination of a scenario affected by Naturally Occurring Radioactive Material (NORM) discharges. The cleaning of uranium isotopes from the area has not taken place as rapidly as expected due to leaching from phosphogypsum stacks. An in-depth study using various techniques of analysis, including 234 U/ 238 U and 230 Th/ 232 Th ratios and the decreasing rates of the uranium concentration, enabled a second source of uranium contamination to be discovered. Increased uranium levels due to acid mine drainage from pyrite mines located in the Iberian Pyrite Belt (SW Spain) prevent complete uranium decontamination and, therefore, result in levels nearly twice those of natural background levels.

A non-pedological hypothesis for the processes of uranium mineralization in calcrete

International Nuclear Information System (INIS)

Briot, P.; Fuchs, Y.

1984-01-01

The non-pedological hypothesis presented for the origin of the uraniferous calcrete deposits in Western Australia is based on the premise that alluvial and calcareous lacustrine sediments were initially formed during earlier wet periods, evidence for which has been found in the fossil records. These were followed by subsequent epigenetic alteration accompanied by the precipitation of uranium mineralization during drier semi-arid periods. Typical examples of the processes involved were found in the Yeelirrie uranium deposit. During the latter semi-arid period, the limited surface flow which consisted of periodic flash flood conditions probably contributed marginally to the recharge of the groundwater, and consequently, semi-stagnant groundwater conditions evolved, particularly where the hydraulic gradient was extremely small, for example, for the Yeelirrie channel it is approximately 0.001. In addition, ponding of water behind a natural barrier caused the groundwater to evolve along the following geochemical sequence: mild alkalinity, weak oxidizing conditions, and oversaturation in dissolved elements. These hydrological and hydrogeochemical conditions induced the epigenetic alteration of the palustral/lacustrine limestone, bringing about dolomite neogenesis and the precipitation of carnotite. The source of the uranium in the calcretes and the groundwater of the Yeelirrie channel is considered to be the weathered outcrops of the breakaways along its margins. The genetic hypothesis proposed in this paper, although somewhat different from those described previously and elsewhere in this volume, could be applied to the other uranium-bearing calcretes in Mauritania, Namibia, and Somalia

Comparative study of uranium concentration in water samples of SW and NE Punjab, India

International Nuclear Information System (INIS)

Saini, Komal; Bajwa, B.S.

2014-01-01

Since the commencement of the earth, radiations and natural radioactivity has always been a part of environment. Uranium is heaviest naturally occurring element which is widespread in nature, mainly occurs in granites mineral deposits. The natural weathering of rocks such as granite dissolves the natural uranium, which goes into groundwater by leaching and precipitation called illumination process. People are always exposed to certain amount of uranium from air, water, soil and food as it is usually present in these components. About 85% of ingested uranium enter into human body through drinking water which makes it very important to estimate uranium concentration in potable water. Uranium and some other heavy metals may increase the risk of kidney damage, cancer diseases where experimental evidence suggests that respiratory and reproductive system are also affected by uranium exposure. In the present study comparative study of uranium concentration in potable water samples of SW and NE Punjab has been analysed

Distribution of natural uranium in groundwater around Kudankulam

International Nuclear Information System (INIS)

Selvi, B.S.; Vijayakumar, B.; Rana, B.K.; Ravi, P.M.

2016-01-01

A systematic study was carried out to estimate the uranium concentration in the ground water around Kudankulam in Southern Tamil Nadu. The uranium concentration in ground water varies from 0.2 to 6.6 μg/l, with a mean value of 2.0 μg/l. The Quantalase uranium analyzer was used to measure the uranium concentration. These groundwater samples were analyzed for the water quality parameters such as pH, conductance, total dissolved solids (TDS), salinity, chloride, and sulfate. An attempt has been made to correlate the uranium concentration with the water quality parameters. It is observed that conductance, TDS, salinity, chloride, and sulfate show positive correlation with uranium concentration. (author)

Natural uranium utilization without enrichment and reprocessing

Energy Technology Data Exchange (ETDEWEB)

Sekimoto, H.; Toshinsky, V.; Ryu, K. [Tokyo Inst. of Tech. (Japan). Research Lab. for Nuclear Reactors

2001-07-01

Two types of fast reactor are investigated to utilize the natural uranium without enrichment and reprocessing in an equilibrium state. The first trial is SFPR. Its fuel-shuffling pattern is optimized. An obtained result gives its peak fuel burnup of 22,5%, power peaking factor of 1.5 and peak excess reactivity of 2,15%. The second trial is CANDLE burnup scheme, where distribution shapes of neutron flux and nuclide densities are constant but move in axial direction with a constant velocity. A feasible solution gives the speed of burning region of 4,1 cm/year, k{sub eff} of 1,02 and average spent fuel burnup of 41%. (author)

Uranium processing developments

International Nuclear Information System (INIS)

Jones, J.Q.

1977-01-01

The basic methods for processing ore to recover the contained uranium have not changed significantly since the 1954-62 period. Improvements in mill operations have been the result of better or less expensive reagents, changes in equipment, and in the successful resolvement of many environmental matters. There is also an apparent trend toward large mills that can profitably process lower grade ores. The major thrust in the near future will not be on process technology but on the remaining environmental constraints associated with milling. At this time the main ''spot light'' is on tailings dam and impoundment area construction and reclamation. Plans must provide for an adequate safety factor for stability, no surface or groundwater contamination, and minimal discharge of radionuclides to unrestricted areas, as may be required by law. Solution mining methods must also provide for plans to restore the groundwater back to its original condition as defined by local groundwater regulations. Basic flowsheets (each to finished product) plus modified versions of the basic types are shown

Rirang uranium ore processing: continuous solvent extraction of uranium from Rirang ore acid digestion solution

International Nuclear Information System (INIS)

Riza, F.; Nuri, H. L.; Waluya, S.; Subijanto, A.; Sarono, B.

1998-01-01

Separation of uranium from Rirang ore acid digestion solution by means of continuous solvent extraction using mixer-settlers has been studied and a mixture of 0.3 M D2EHPA and 0.075 M TOPO extracting agent and kerosene diluent is employed to recover and separate uranium from Th, RE, phosphate containing solution. The experiments have been conducted batch-wise and several parameters have been studied including the aqueous to organic phase ratio, A/O, the extraction and the stripping times, and the operation temperature. The optimum conditions for extraction have been found to be A/O = 2 ratio, five minute extraction time per stage at room temperature. The uranium recovery of 99.07% has been achieved at those conditions whilst U can be stripped from the organic phase by 85% H 3 PO 4 solution with an O/A = 1 for 5 minutes stripping time per stage, and in a there stage operation at room temperature yielding a 100% uranium recovery from the stripping process

Uranium

International Nuclear Information System (INIS)

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

2010-01-01

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

Process evaluations for uranium recovery from scrap material

International Nuclear Information System (INIS)

Westphal, B.R.; Benedict, R.W.

1992-01-01

The integral Fast Reactor (IFR) concept being developed by Argonne National Laboratory is based on pyrometallurgical processing of spent nuclear metallic fuel with subsequent fabrication into new reactor fuel by an injection casting sequence. During fabrication, a dilute scrap stream containing uranium alloy fines and broken quartz (Vycor) molds in produced. Waste characterization of this stream, developed by using present operating data and chemical analysis was used to evaluate different uranium recovery methods and possible process variations for the return of the recovered metal. Two methods, comminution with size separation and electrostatic separation, have been tested and can recover over 95% of the metal. Recycling the metal to either the electrochemical process or the injection casting was evaluated for the different economic and process impacts. The physical waste parameters and the important separation process variables are discussed with their effects on the viability of recycling the material. In this paper criteria used to establish the acceptable operating limits is discussed

EFFECT OF CURRENT, TIME, FEED AND CATHODE TYPE ON ELECTROPLATING PROCESS OF URANIUM SOLUTION

Directory of Open Access Journals (Sweden)

Sigit Sigit

2017-02-01

Full Text Available ABSTRACT   EFFECT OF CURRENT, TIME, FEED AND CATHODE TYPE ON ELECTROPLATING PROCESS OF URANIUM SOLUTION. Electroplating process of uranyl nitrate and effluent process has been carried out in order to collect uranium contained therein using electrode Pt / Pt and Pt / SS at various currents and times. Material used for electrode were Pt (platinum and SS (Stainlees Steel. Feed solution of 250 mL was entered into a beaker glass equipped with Pt anode - Pt cathode or Pt anode - SS cathode, then fogged direct current from DC power supply with specific current and time so that precipitation of uranium sticking to the cathode. After the processes completed, the cathode was removed and weighed to determine weight of precipitates, while the solution was analyzed to determine the uranium concentration decreasing after and before electroplating process. The experiments showed that a relatively good time to acquire uranium deposits at the cathode was 1 hour by current 7 ampere, uranyl nitrate as feed, and Pt (platinum as cathode. In these conditions, uranium deposits attached to the cathode amounted to 74.96% of the original weight of uranium oxide in the feed or 206.5 mg weight. The use of Pt cathode for  uranyl nitrate, SS and Pt cathode for effluent process feed gave uranium specific weight at the cathode of 12.99 mg/cm2, 2.4 mg/cm2 and 5.37 mg/cm2 respectively for current 7 ampere and electroplating time 1 hour. Keywords: Electroplating, uranyl nitrate, effluent process, Pt/Pt electrode, Pt/SS electrode

Non-filtration method of processing of uranium ores

International Nuclear Information System (INIS)

Laskorin, B.N.; Vodolazov, L.I.; Tokarev, N.N.; Vyalkov, V.I.; Goldobina, V.A.; Gosudarstvennyj Komitet po Ispol'zovaniyu Atomnoj Ehnergii SSSR, Moscow)

1977-01-01

The development of the filterless sorption method has lead to working out the sorption leaching process and the process of extraction desorption, which has made possible to intensify the process of uranium ore working and to improve greatly the technical economic indexes by liquidating the complex method of multiple filtration and repulping of cakes. This method makes possible to involve more poor uranium raw materials and at the same time to extract valuable components: molybdenum, vanadium, copper, etc. Great industrial experience has been accumulating in sorption of dense pulp with the ratio of solid phase to liquid one equal to 1:1. This has lead to the increase of productivity of working plants by 1,5-3,0 times, the increase of uranium extraction by 5-10%, the increase of labour capacity of main workers by 2-3 times, and to the decrease of reagents expense, auxiliary materials, electric energy and vapour by several times. In fact the developed technology is continuous in all its steps with complete complex automatization of the process with the help of the most simple and available means of regulation and controlling. The process is equipped with high productivity apparatuses of great power with mechanic and pneumatic mixing for high density pulps, and with the columns KDS, KDZS, KNSPR and PIK for the regeneration of saturated sorbent in the counterflow regime. The exploitation of fine-granular hydrophilic ion-exchange resins in hydrophobized state is foreseen [ru

Optimization of desalting process with centrifugation for condensation process of uranium from sea water

International Nuclear Information System (INIS)

Yamamoto, Tatsuya; Takase, Hisao; Fukuoka, Fumio

1984-01-01

Optimization of desalting of the slurry on the condensation process by the deposited slurry method for the recovery of uranium from sea water was studied. We have already published that the uranium rich deposit containing seven ppm uranium could be made on the sea bottom by the deposited slurry method. Uranium can be transferred to the anion exchange resin from titanic acid in the slurry. But in this case Cl - ions obstruct the adsorption of uranium on the anion exchange resin, so the slurry must be desalted before RIP method. It is considered that the cost of desalting of the slurry stage would be a large portion of the capital cost for the recovery of uranium from sea water. The cost of water required is comparable to the cost of energy so that the objective function consists of the cost of energy and the quantity of water. The consumption of energy and water required for desalting of the slurry with the multi-stage centrifugation were oprimized based on dynamic programming. (author)

Process of recovering uranium from wet process acid

International Nuclear Information System (INIS)

York, W.R.

1983-01-01

Entrainment of contaminated water in the organic phase and poor phase disengagement is prevented in the second cycle scrubber, in a two cycle uranium recovery process, by washing the organic solvent stream containing entrained H 3 PO 4 from the second cycle extractor, with a dilute aqueous sulfuric or nitric acid solution in an acid scrubber, prior to passing the solvent stream into the second cycle stripper. (author)

Depleted uranium plasma reduction system study

International Nuclear Information System (INIS)

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

1994-12-01

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

A plant taxonomic survey of the Uranium City region, Lake Athabasca north shore, emphasizing the naturally colonizing plants on uranium mine and mill wastes and other human-disturbed sites

International Nuclear Information System (INIS)

Harms, V.L.

1982-07-01

A goal of this study was to acquire more complete baseline data on the existing flora of the Uranium City region, both in natural and human-disturbed sites. Emphasis was given to determining which plant species were naturally revegetating various abandoned uranium mine and mill waste disposal areas, other human-disturbed sites, and ecologically analogous sites. Another goal was to document the occurrence and distribution in the study region of rare and possibly endangered species. A further objective was to suggest regionally-occurring species with potential value for revegetating uranium mine and mill waste sites. Field investigations were carried out in the Uranium City region during August, 1981. During this time 1412 plant collections were made; a total of 366 plant species - trees, shrubs, forbs, graminoids, lichens, and bryophytes were recorded. The report includes an annotated checklist of plant species of the Uranium City region and a reference index of plant taxa indicating species that have high revegetation potential

Analytical strategies for uranium determination in natural water and industrial effluents samples

International Nuclear Information System (INIS)

Santos, Juracir Silva

2011-01-01

The work was developed under the project 993/2007 - 'Development of analytical strategies for uranium determination in environmental and industrial samples - Environmental monitoring in the Caetite city, Bahia, Brazil' and made possible through a partnership established between Universidade Federal da Bahia and the Comissao Nacional de Energia Nuclear. Strategies were developed to uranium determination in natural water and effluents of uranium mine. The first one was a critical evaluation of the determination of uranium by inductively coupled plasma optical emission spectrometry (ICP OES) performed using factorial and Doehlert designs involving the factors: acid concentration, radio frequency power and nebuliser gas flow rate. Five emission lines were simultaneously studied (namely: 367.007, 385.464, 385.957, 386.592 and 409.013 nm), in the presence of HN0 3 , H 3 C 2 00H or HCI. The determinations in HN0 3 medium were the most sensitive. Among the factors studied, the gas flow rate was the most significant for the five emission lines. Calcium caused interference in the emission intensity for some lines and iron did not interfere (at least up to 10 mg L -1 ) in the five lines studied. The presence of 13 other elements did not affect the emission intensity of uranium for the lines chosen. The optimized method, using the line at 385.957 nm, allows the determination of uranium with limit of quantification of 30 μg L -1 and precision expressed as RSD lower than 2.2% for uranium concentrations of either 500 and 1000 μg L -1 . In second one, a highly sensitive flow-based procedure for uranium determination in natural waters is described. A 100-cm optical path flow cell based on a liquid-core waveguide (LCW) was exploited to increase sensitivity of the arsenazo 111 method, aiming to achieve the limits established by environmental regulations. The flow system was designed with solenoid micro-pumps in order to improve mixing and minimize reagent consumption, as well as

Yellowcake processing in uranium recovery

International Nuclear Information System (INIS)

Paul, J.M.

1981-01-01

This information relates to the recovery of uranium from uranium peroxide yellowcake produced by precipitation with hydrogen peroxide. The yellowcake is calcined at an elevated temperature to effect decomposition of the yellowcake to uranium oxide with the attendant evolution of free oxygen. The calcination step is carried out in the presence of a reducing agent which reacts with the free oxygen, thus retarding the evolution of chlorine gas from sodium chloride in the yellowcake. Suitable reducing agents include ammonia producing compounds such as ammonium carbonate and ammonium bicarbonate. Ammonium carbonate and/or ammonium bicarbonate may be provided in the eluant used to desorb the uranium from an ion exchange column

Yellowcake processing in uranium recovery

Energy Technology Data Exchange (ETDEWEB)

Paul, J.M.

1981-10-06

This information relates to the recovery of uranium from uranium peroxide yellowcake produced by precipitation with hydrogen peroxide. The yellowcake is calcined at an elevated temperature to effect decomposition of the yellowcake to uranium oxide with the attendant evolution of free oxygen. The calcination step is carried out in the presence of a reducing agent which reacts with the free oxygen, thus retarding the evolution of chlorine gas from sodium chloride in the yellowcake. Suitable reducing agents include ammonia producing compounds such as ammonium carbonate and ammonium bicarbonate. Ammonium carbonate and/or ammonium bicarbonate may be provided in the eluant used to desorb the uranium from an ion exchange column.

Analysis of fuel cycles with natural uranium, Phase I; Analiza gorivnih ciklusa sa prirodnim uranom, I faza

Energy Technology Data Exchange (ETDEWEB)

Stojadinovic, A; Zivkovic, Z; Raisic, N [Institute of Nuclear Sciences Boris Kidric, Laboratorija za fiziku i dinamiku reaktora, Vinca, Beograd (Serbia and Montenegro)

1964-12-15

This paper contains analyses of fuel cycles with natural uranium for the following cases: plutonium recycling is not done; recycling of plutonium and irradiated uranium with the condition of equal multiplication factor at the beginning of each cycle; and recycling of plutonium only.

Bioleaching - an alternate uranium ore processing technology for India

International Nuclear Information System (INIS)

Abilash; Mehta, K.D.; Kumar, V.; Pandey, B.D.; Tamarakar, P.K.

2010-01-01

Meeting the feed supply of uranium fuel in the present and planned nuclear reactors calls for huge demand of uranium, which at the current rate of production, shows a mismatch. The processing methods at UCIL (DAE) needs to be modified/changed or re-looked into because of its very suitability in near future for low-index raw materials which are either unmined or stacked around if mined. There is practically no way to process tailings with still some values. Efforts were made to utilize such resources (low-index ore of Turamdih mines, containing 0.03% U 3 O 8 ) by NML in association with UCIL as a national endeavor. In this area, the R and D work showed the successful development of a bioleaching process from bench scale to lab scale columns and then finally to the India's first ever large scale column, from the view point of harnessing such a processing technology as an alternative for the uranium industry and nuclear sector in the country. The efforts culminated into the successful operation of large scale trials at the 2 ton level column uranium bioleaching that was carried out at the site of UCIL, Jaduguda yielding a maximum recovery of 69% in 60 days. This achievement is expected to pave the way for scaling up the activity to a 100T or even more heap bioleaching trials for realization of this technology, which needs to be carried out with the support of the nuclear sector in the country keeping in mind the national interest. (author)

Study on extraction of uranium from clayey sandstone with floatation-leaching process

International Nuclear Information System (INIS)

Meng Guangshou; Zhao Manchang; Wu Peisheng; Song Wenlan; Li Wenxia.

1985-01-01

An improved floatation-leaching process is proposed to extract uranium from some clayey sandstone type of ore. By two-step flotation, the ground feed ore can be divided into three urani-ferous sections, i.e., the sulfidic concentrate carrying organic matter, the carbonate concentrate, and the tailings. The sulfidic concentrate is mixed with the tailings and then treated by acid-leaching with the result that 93% uranium extraction can be attained. The excess free acid of the leached slurry is further neutralized with the carbonate concentrate instead of lime commonly used. As a result, approximately 60% uranium extraction can be attained. As a whole, by the flotation-leaching process the acid consumption can be reduced from 200 kg/t down to < 80 kg/t and the uranium extraction can be raised from 85% to 90% as compared with the conventional acid-leaching process

Recovery of uranium in the production of concentrated phosphoric acid by a hemihydrate process

International Nuclear Information System (INIS)

Nakajima, S.; Miyamoto, M.

1983-01-01

Nissan Chemical Industries as manufacturers of phosphoric acid have studied the recovery of uranium, based on a concentrated phosphoric acid production process. The process consists of two stages, a hemihydrate stage with a formation of hemihydrate and a filtration section, followed by a dihydrate stage with hydration and a filtration section. In the hemihydrate stage, phosphate is treated with a mixture of phosphoric acid and sulphuric acid to produce phosphoric acid and hydrous calcium sulphate; the product is recovered in the filtration section and its concentration is 40-50% P 2 O 3 . In the dihydrate stage, the hemihydrate is transformed by re-dissolution and hydration, producing hydrous calcium sulphate, i.e. gypsum. This process therefore comprises two parts, each with different acid concentrations. As the extraction of uranium is easier in the case of a low concentration of phosphoric acid, the process consists of the recovery of uranium starting from the filtrate of the hydration section. The tests have shown that the yield of recovery of uranium was of the order of 80% disregarding the handling losses and no disadvantageous effect has been found in the combination of the process of uranium extraction with the process of concentrated phosphoric acid production. Compared with the classical process where uranium is recovered from acid with 30% P 2 O 5 , the process of producing high-concentration phosphoric acid such as the Nissan process, in which the uranium recovery is effected from acid with 15% P 2 O 5 from the hydration section, presents many advantages [fr

Radon 226 and natural Uranium in potable waters to the Argentina Republic

International Nuclear Information System (INIS)

Bomben, A.M.; Palacios, M.A.

1998-01-01

157 samples were analyzed in the Buenos Aires City. Gathered in the domiciliary distribution net and private wells. The radon 226 concentration to determines for the radon 226 emanation technique and liquid scintilligraphy. The natural uranium concentration one carries out for fluorimetric methods

Natural uranium metallic fuel elements: fabrication and operating experience

International Nuclear Information System (INIS)

Hammad, F.H.; Abou-Zahra, A.A.; Sharkawy, S.W.

1980-01-01

The main reactor types based on natural uranium metallic fuel element, particularly the early types, are reviewed in this report. The reactor types are: graphite moderated air cooled, graphite moderated gas cooled and heavy water moderated reactors. The design features, fabrication technology of these reactor fuel elements and the operating experience gained during reactor operation are described and discussed. The interrelation between operating experience, fuel design and fabrication was also discussed with emphasis on improving fuel performance. (author)

Status Report from Yugoslavia [Processing of Low-Grade Uranium Ores

Energy Technology Data Exchange (ETDEWEB)

Bunji, B [Institute for Technology of Nuclear and Other Raw Materials, Belgrade, Yugoslavia (Serbia)

1967-06-15

Full text: The greater part of our activities is connected with the problem of extracting uranium from low-grade ores. In this paper, a brief review of the most important recent developments will be presented. In this connection, it may be useful to determine the definition of low-grade ores. This term can be applied to ore from which the uranium content cannot be extracted under normal economic conditions. Thus this term can be applied to uranium-bearing material with a uranium content of no more than 0. 05%. But, in general, it could be said that there is a very large range of uranium content where uranium extraction may not be economic for such different reasons as; (a) the size or other facts in connection with the orebodies themselves; (b) refractory ore; or (c) other local conditions. During research on the treatment of low-grade ore from the deposit at Gabrovnica (Stara Planina, Yugoslavia) it became apparent that an alkaline leaching process would have to be carried out. The treatment of this granitic type of ore causes no particular difficulties. The required temperature is about 90{sup o}C. The retention time in the leaching stage is from 4 to 12 hours. Sodium carbonate consumption is not higher than 15 kg/t of ore. Pachuca-type leaching shows satisfactory maintenance and processing costs. At Kalna uranium precipitation by means of hydrogen pressure reduction has been developed, and is being developed and investigated in full-scale operation. Details of the process were published in Geneva in 1963. On the basis of the experience gained from full-scale operation, many refinements and cost-saving changes have been made. A normal steel wire screen used as a catalyst carrier shows a very good improvement over free-moving UO{sub 2} as catalyst. In large-scale operation (200 t/d), after the precipitation of uranium the barren solution content is about 1 g U/m{sup 3}. The content of the pregnant solution is of the order of 300-600 g/m{sup 3}. Recycling the

Determination of natural uranium in urine (233U)

International Nuclear Information System (INIS)

Jeanmaire, L.; Jammet, H.

1959-01-01

A procedure for the quantitative analysis of uranium in urine is described. The residue obtained by mineralization is dissolved in diluted hydrochloric acid. Uranium is separated by fixation on a permutit 50 column, elution with 0,2 M oxalic acid and electrodeposition on nickel. Uranium is then measured by α counting. It is thus possible to detect less than 1 pico-curie of uranium in the sample. (author) [fr

Developments in natural uranium - graphite reactors; Developpement des reacteurs a graphite et uranium naturel

Energy Technology Data Exchange (ETDEWEB)

Bourgeois, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires; Saitcevsky, B [Electricite de France (EDF), 75 - Paris (France)

1964-07-01

The French natural uranium-graphite power-reactor programme has been developing - from EDF 1 to EDF 4 - in the direction of an increase of the unit power of the installations, of the specific and volume powers, and of an improvement in the operational security conditions. The high power of EDF 4 (500 MWe) and the integration of the primary circuit into the reactor vessel, which is itself made of pre-stressed concrete, make it possible to make the most of the annular fuel elements already in use in EDF 1, and to arrive thus at a very satisfactory solution. The use of an internally cooled fuel element (an annular element) has led to a further step forward: it now becomes possible to increase the pressure of the cooling gas without danger of causing creep in the uranium tube. The use of a pre-stressed concrete vessel makes this pressure increase possible, and the integration of the primary circuit avoids the risk of a rapid depressurization which would be in this case a major danger. This report deals with the main problems presented by this new type of nuclear power station, and gives the main lines of research and studies now being carried out in France. - Neutronic and thermal research has made it possible to consider using large size fuel elements (internal diameter = 77 mm, external diameter 95 mm) while still using natural uranium. - The problems connected with the production of these elements and with their in pile behaviour are the subject of a large programme, both out of pile and in power reactors (EDF 2) and test reactors (Pegase). - The increase in the size of the element leads to a large lattice pitch (35 to 40 cm). This makes it possible to consider having one charging aperture per channel or for a small number of channels, whether the charge machine be inside or outside the pressure vessel. In conclusion are given the main characteristics of a project for a 500 MWe power station using such a fuel element. In particular this project is compared to EDF 4

Measures for waste water management from recovery processing of Zhushanxia uranium deposit

International Nuclear Information System (INIS)

Liu Yaochi; Xu Lechang

2000-01-01

Measures for waste water management from recovery processing of Zhushanxia uranium deposit of Wengyuan Mine is analyzed, which include improving process flow, recycling process water used in uranium mill as much as possible and choosing a suitable disposing system. All these can decrease the amount of waste water, and also reduce costs of disposing waste water and harm to environment

Human resource development for uranium production cycle

International Nuclear Information System (INIS)

Ganguly, C.

2014-01-01

Nuclear fission energy is a viable option for meeting the ever increasing demand for electricity and high quality process heat in a safe, secured and sustainable manner with minimum carbon foot print and degradation of the environment. The growth of nuclear power has shifted from North America and Europe to Asia, mostly in China and India. Bangladesh, Vietnam, Indonesia, Malaysia and the United Arab Emirates are also in the process of launching nuclear power program. Natural uranium is the basic raw material for U-235 and Pu-239, the fuels for all operating and upcoming nuclear power reactors. The present generation of nuclear power reactors are mostly light water cooled and moderated reactor (LWR) and to a limited extent pressurized heavy water reactor (PHWR). The LWRs and PHWRs use low enriched uranium (LEU with around 5% U-235) and natural uranium as fuel in the form of high density UO_2 pellets. The uranium production cycle starts with uranium exploration and is followed by mining and milling to produce uranium ore concentrate, commonly known as yellow cake, and ends with mine and mill reclamation and remediation. Natural uranium and its daughter products, radium and radon, are radioactive and health hazardous to varying degrees. Hence, radiological safety is of paramount importance to uranium production cycle and there is a need to review and share best practices in this area. Human Resource Development (HRD) is yet another challenge as most of the experts in this area have retired and have not been replaced by younger generation because of the continuing lull in the uranium market. Besides, uranium geology, exploration, mining and milling do not form a part of the undergraduate or post graduate curriculum in most countries. Hence, the Technical Co-operation activities of the IAEA are required to be augmented and more country specific and regional training and workshop should be conducted at different universities with the involvement of international experts

Waste monitoring of the uranium ore processing activities in Romania

International Nuclear Information System (INIS)

Nica, L.

2002-01-01

The uranium ore processing activities at the Feldioara site produce a range of liquid and solid waste that are monitored. Liquids are treated through decantation, pH correction and uranium precipitation before their release into the environment. The solid waste is gathered into ore specific area and are covered regularly with clay materials. (author)

The physics of uranium isotope separation by laser

International Nuclear Information System (INIS)

Clerc, M.; Rigny, P.

1985-01-01

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

Use of enriched uranium in Canada's power reactors

International Nuclear Information System (INIS)

Dormuth, K.W.; Jackson, D.P.

2011-01-01

Recent trends in Canadian nuclear power reactor design and proposed development of nuclear power in Canada have indicated the possibility that Canada will break with its tradition of natural uranium fuelled systems, designed for superior neutron economy and, hence, superior uranium utilization. For instance, the Darlington B new reactor project procurement process included three reactor designs, all employing enriched fuel, although a natural uranium reactor design was included at a late stage in the ensuing environmental assessment for the project as an alternative technology. An evaluation of the alternative designs should include an assessment of the environmental implications through the entire fuel cycle, which unfortunately is not required by the environmental assessment process. Examples of comparative environmental implications of the reactor designs throughout the fuel cycle indicate the importance of these considerations when making a design selection. As Canada does not have enrichment capability, a move toward the use of enriched fuel would mean that Canada would be exporting natural uranium and buying back enriched uranium with value added. From a waste management perspective, Canada would need to deal with mill, refinery, and conversion tailings, as well as with the used fuel from its own reactors, while the enrichment supplier would retain depleted uranium with some commercial value. On the basis of reasoned estimates based on publicly available information, it is expected that enrichment in Canada is likely to be more profitable than exporting natural uranium and buying back enriched uranium. Further, on the basis of environmental assessments for enrichment facilities in other countries, it is expected that an environmental assessment of a properly sited enrichment facility would result in approval. (author)

Assay of uranium in fused salt cake generated at the natural uranium metal fuel fabrication plants by gamma-ray spectrometry

International Nuclear Information System (INIS)

Kalsi, P.C.; Bhanu, A.U.; Sahoo, S.; Iyer, R.H.

1986-01-01

A passive gamma-ray spectroscopic method is employed for the assay of uranium in fused salt cake, a scrap produced at the natural uranium metal fuel fabrication plants. The method makes use of NaI(TI) detector coupled with a multichannel analyser. The 1 MeV gamma-ray of 238 U was used for the calibration. The calibration curve was made by counting synthetic mixtures made of U 3 O 8 powder, the heat treatment salt and iron in the form of fine powder. The uranium content in these synthetic mixtures was kept in the range of 1-11 per cent. 23 lots of the fused salt cake taken from three different batches of the salt cake were then analysed by this method. The uranium content of fused salt cake was found to be in the range of 1.70-11.43 per cent. To compare the gamma spectrometric results with a completely independent method, chemical analysis of all the fused salt cakes were also carried out. The NDA results were found to agree within ± 17 per cent with the chemical analysis results. (author)

Erosional stability of rehabilitated uranium mine structures incorporating natural landform characteristics, northern tropical Australia

International Nuclear Information System (INIS)

East, T.J.; Uren, C.J.; Noller, B.N.; Cull, R.F.; Curley, P.M.; Unger, C.J.

1994-01-01

Australian Government guidelines specify that tailings containment structures at rehabilitated uranium mines in the Alligator Rivers Region of tropical northern Australia should have an engineered structural life of 1000 years. As part of the containment structure design process, erosion plots incorporating both regional geomorphological characteristics (concave hillslope profiles and a weathering-resistant rock cover of schist) and more conventional engineering design parameters (straight slopes and mine waste rock) were constructed at the Ranger Uranium Mine. The plots were monitored for storm runoff, and concentrations of solutes, suspended solids and selected ions over successive wet seasons. The concave slopes (the hillslope analogues) had lower peak discharges and lower concentrations of suspended solids than the straight slopes. However, solute concentrations in runoff from the schist covered (hillslope) slopes were higher than from the waste rock covered plots. Solute (mainly magnesium sulfate) concentrations for both rock types decreased by about an order of magnitude over the wet season. High sulfate concentrations are also likely to decrease substantially after several wet seasons, due to settlement of the waste rock and a reduction in rates of weathering. Development of a vegetation cover on the rehabilitated landforms will reduce the high suspended sediment concentrations. These initial results suggest that rehabilitated uranium mine structures which utilise selected features of stable natural landforms in their design may have greater erosional stability than more conventionally engineered structures. (orig.)

Model of a Generic Natural Uranium Conversion Plant ? Suggested Measures to Strengthen International Safeguards

Energy Technology Data Exchange (ETDEWEB)

Raffo-Caiado, Ana Claudia [ORNL; Begovich, John M [ORNL; Ferrada, Juan J [ORNL

2009-11-01

This is the final report that closed a joint collaboration effort between DOE and the National Nuclear Energy Commission of Brazil (CNEN). In 2005, DOE and CNEN started a collaborative effort to evaluate measures that can strengthen the effectiveness of international safeguards at a natural uranium conversion plant (NUCP). The work was performed by DOE s Oak Ridge National Laboratory and CNEN. A generic model of a NUCP was developed and typical processing steps were defined. Advanced instrumentation and techniques for verification purposes were identified and investigated. The scope of the work was triggered by the International Atomic Energy Agency s 2003 revised policy concerning the starting point of safeguards at uranium conversion facilities. Prior to this policy only the final products of the uranium conversion plant were considered to be of composition and purity suitable for use in the nuclear fuel cycle and therefore, subject to the IAEA safeguards control. DOE and CNEN have explored options for implementing the IAEA policy, although Brazil understands that the new policy established by the IAEA is beyond the framework of the Quadripartite Agreement of which it is one of the parties, together with Argentina, the Brazilian-Argentine Agency for Accounting and Control of Nuclear Materials (ABACC) and the IAEA. Two technical papers on this subject were published at the 2005 and 2008 INMM Annual Meetings.

Determination of uranium and plutonium in metal conversion products from electrolytic reduction process

International Nuclear Information System (INIS)

Lee, Chang Heon; Suh, Moo Yul; Joe, Kih Soo; Sohn, Se Chul; Jee, Kwang Young; Kim, Won Ho

2005-01-01

Chemical characterization of process materials is required for the optimization of an electrolytic reduction process in which uranium dioxide, a matrix of spent PWR fuels, is electrolytically reduced to uranium metal in a medium of LiCl-Li 2 O molten at 650 .deg. C. A study on the determination of fissile materials in the uranium metal products containing corrosion products, fission products and residual process materials has been performed by controlled-potential coulometric titration which is well known in the field of nuclear science and technology. Interference of Fe, Ni, Cr and Mg (corrosion products), Nd (fission product) and LiCl molten salt (residual process material) on the determination of uranium and plutonium, and the necessity of plutonium separation prior to the titration are discussed in detail. Under the analytical condition established already, their recovery yields are evaluated along with analytical reliability

Surveying and assessing the hazards associated with the processing of uranium

International Nuclear Information System (INIS)

Kruger, J.

1980-01-01

The control of uranium during the milling process has not received extensive attention. The results of several surveys of surface contamination, airborne contamination and external radiation made at South African processing facilities are presented and compared with derived norms for permissible exposure to uranium dust. The routine urine sampling results are used as an indicator of personnel exposures. Results of sampling identify the main sources of airborne activity and indicate the contribution of general surface contamination levels to airborne levels. The use of surface contamination levels together with frequent air sampling for assessing the environmental conditions is illustrated. It is concluded that infrequent grab air sampling alone is not adequate for assessing the hazards during uranium processing. Detailed surveys are required and proper area and personnel access control are indicated. (H.K.)

Criticality accident in uranium fuel processing plant. The estimation of the total number of fissions with related reactor physics parameters

International Nuclear Information System (INIS)

Nishina, Kojiro; Oyamatsu, Kazuhiro; Kondo, Shunsuke; Sekimoto, Hiroshi; Ishitani, Kazuki; Yamane, Yoshihiro; Miyoshi, Yoshinori

2000-01-01

This accident occurred when workers were pouring a uranium solution into a precipitation tank with handy operation against the established procedure and both the cylindrical diameter and the total mass exceeded the limited values. As a result, nuclear fission chain reactor in the solution reached not only a 'criticality' state continuing it independently but also an instantly forming criticality state exceed the criticality and increasing further nuclear fission number. The place occurring the accident at this time was not reactor but a place having not to form 'criticality' called by a processing process of uranium fuel. In such place, as because of relating to mechanism of chain reaction, it is required naturally for knowledge on the reactor physics, it is also necessary to understand chemical reaction in chemical process, and functions of tanks, valves and pumps mounted at the processes. For this purpose, some information on uranium concentration ratio, atomic density of nuclides largely affecting to chain reaction such as uranium, hydrogen, and so forth in the solution, shape, inner structure and size of container for the solution, and its temperature and total volume, were necessary for determining criticality volume of the accident uranium solution by using nuclear physics procedures. Here were described on estimation of energy emission in the JCO accident, estimation from analytical results on neutron and solution, calculation of various nuclear physics property estimation on the JCO precipitation tank at JAERI. (G.K.)

Development of a recovery process of scraps resulting from the manufacture of metallic uranium fuels

International Nuclear Information System (INIS)

Camilo, Ruth L.; Kuada, Terezinha A.; Forbicini, Christina A.L.G.O.; Cohen, Victor H.; Araujo, Bertha F.; Lobao, Afonso S.T.

1996-01-01

The study of the dissolution of natural metallic uranium fuel samples with aluminium cladding is presented, in order to obtain optimized conditions for the system. The aluminium cladding was dissolved in an alkaline solution of Na OH/Na NO 3 and the metallic uranium with HNO 3 . A fumeless dissolution with total recovery of nitrous gases was achieved. The main purpose of this project was the recovery of uranium from scraps resulting from the manufacture of the metallic uranium fuel or other non specified fuels. (author)

Determination of irradiated reactor uranium in soil samples in Belarus using 236U as irradiated uranium tracer.

Science.gov (United States)

Mironov, Vladislav P; Matusevich, Janna L; Kudrjashov, Vladimir P; Boulyga, Sergei F; Becker, J Sabine

2002-12-01

This work presents experimental results on the distribution of irradiated reactor uranium from fallout after the accident at Chernobyl Nuclear Power Plant (NPP) in comparison to natural uranium distribution in different soil types. Oxidation processes and vertical migration of irradiated uranium in soils typical of the 30 km relocation area around Chernobyl NPP were studied using 236U as the tracer for irradiated reactor uranium and inductively coupled plasma mass spectrometry as the analytical method for uranium isotope ratio measurements. Measurements of natural uranium yielded significant variations of its concentration in upper soil layers from 2 x 10(-7) g g(-1) to 3.4 x 10(-6) g g(-1). Concentrations of irradiated uranium in the upper 0-10 cm soil layers at the investigated sampling sites varied from 5 x 10(-12) g g(-1) to 2 x 10(-6) g g(-1) depending on the distance from Chernobyl NPP. In the majority of investigated soil profiles 78% to 97% of irradiated "Chernobyl" uranium is still contained in the upper 0-10 cm soil layers. The physical and chemical characteristics of the soil do not have any significant influence on processes of fuel particle destruction. Results obtained using carbonate leaching of 236U confirmed that more than 60% of irradiated "Chernobyl" uranium is still in a tetravalent form, ie. it is included in the fuel matrix (non-oxidized fuel UO2). The average value of the destruction rate of fuel particles determined for the Western radioactive trace (k = 0.030 +/- 0.005 yr(-1)) and for the Northern radioactive trace (k = 0.035 + 0.009 yr(-1)) coincide within experimental errors. Use of leaching of fission products in comparison to leaching of uranium for study of the destruction rate of fuel particles yielded poor coincidence due to the fact that use of fission products does not take into account differences in the chemical properties of fission products and fuel matrix (uranium).

Some aspects of the processing development for uranium ores treatment

International Nuclear Information System (INIS)

Bruno, J.B.

1982-01-01

It is discussed the methodology adopted by NUCLEBRAS to the processing development for uranium ores treatment. The used methodology has the following steps: exploratories studies, preliminaries stiudies and optimization studies. The studies include physical and chemical contained in the solution. As examples are cited the uranium ores treatment in Lagoa Real and Itataia. (A.B.) [pt

Converting the Caetité Mill Process to Enhance Uranium Recovery and Expand Production

Energy Technology Data Exchange (ETDEWEB)

Gomiero, L. A.; Scassiotti Filho, W.; Veras, A., E-mail: gomiero@inb.gov.br [Indústrias Nucleares do Brasil S/A — INB, Caetité, BA (Brazil); Cunha, J. W. [Instituto de Engenharia Nuclear-IEN/CNEN, Rio de Janeiro, RJ (Brazil); Morais, C. A. [Centro do Desenvolvimento da Tec. Nuclear-CDTN/CNEN, Belo Horizonte, MG (Brazil)

2014-05-15

The Caetité uranium mill was commissioned in 2000 to produce about 340 t U per year from an uranium ore averaging 0.29% U{sub 3}O{sub 8}. This production is sufficient to supply the two operating nuclear power plants in the country. As the Brazilian government has recently confirmed its plan to start building another ones from 2009, the uranium production will have to expand its capacity in the next two years. This paper describes the changes in the milling process that are being evaluated in order to not only increase the production but also the uranium recovery, to fulfil the increasing local demand. The heap leaching process will be changed to conventional tank agitated leaching of ground ore slurry in sulphuric acid medium. Batch and pilot plant essays have shown that the uranium recovery can increase from the 77% historical average to about 93%. As the use of sodium chloride as the stripping agent has presented detrimental effects in the extraction and stripping process, two alternatives are being evaluated for the uranium recovery from the PLS: (a) uranium peroxide precipitation at controlled pH from a PLS that was firstly neutralized and filtered. Batch essays have shown good results with a final calcined precipitate averaging 99% U{sub 3}O{sub 8}. Conversely the results obtained at the first pilot plant essay has shown that the precipitation conditions of the continuous process calls for further evaluation. The pilot plant is being improved and another essay will be carried out. (b) uranium extraction with a tertiary amine followed by stripping with concentrated sulphuric acid solution. Efforts are being made to recover the excess sulphuric acid from the pregnant stripping solution to enhance the economic viability of the process and to avoid the formation of a large quantity of gypsum in the pre-neutralization step before the uranium peroxide precipitation. (author)

Applications of Ecological Engineering Remedies for Uranium Processing Sites, USA

Energy Technology Data Exchange (ETDEWEB)

Waugh, William [Navarro Research and Engineering

2016-05-23

The U.S. Department of Energy (USDOE) is responsible for remediation of environmental contamination and long-term stewardship of sites associated with the legacy of nuclear weapons production during the Cold War in the United States. Protection of human health and the environment will be required for hundreds or even thousands of years at many legacy sites. USDOE continually evaluates and applies advances in science and technology to improve the effectiveness and sustainability of surface and groundwater remedies (USDOE 2011). This paper is a synopsis of ecological engineering applications that USDOE is evaluating to assess the effectiveness of remedies at former uranium processing sites in the southwestern United States. Ecological engineering remedies are predicated on the concept that natural ecological processes at legacy sites, once understood, can be beneficially enhanced or manipulated. Advances in tools for characterizing key processes and for monitoring remedy performance are demonstrating potential. We present test cases for four ecological engineering remedies that may be candidates for international applications.

Conceptual design study on very small long-life gas cooled fast reactor using metallic natural Uranium-Zr as fuel cycle input

International Nuclear Information System (INIS)

Monado, F.; Permana, S.

2013-01-01

Full-text: A conceptual design study of very small 350 MWth Gas-cooled Fast Reactors with Helium coolant has been performed. In this study Modified CANDLE burn-up scheme was implemented to create small and long life fast reactors with natural Uranium as fuel cycle input. Such system can utilize natural Uranium resources efficiently without the necessity of enrichment plant or reprocessing plant. The core with metallic fuel based was subdivided into 10 regions with the same volume. The fresh Natural Uranium is initially put in region-1, after one cycle of 10 years of burn-up it is shifted to region-2 and the each region-1 is filled by fresh Natural Uranium fuel. This concept is basically applied to all axial regions. The reactor discharge burn-up is 31.8 % HM. From the neutronic point of view, this design is in compliance with good performance. (author)

Conceptual design study on very small long-life gas cooled fast reactor using metallic natural Uranium-Zr as fuel cycle input

International Nuclear Information System (INIS)

Monado, Fiber; Ariani, Menik; Su'ud, Zaki; Waris, Abdul; Basar, Khairul; Permana, Sidik; Aziz, Ferhat; Sekimoto, Hiroshi

2014-01-01

A conceptual design study of very small 350 MWth Gas-cooled Fast Reactors with Helium coolant has been performed. In this study Modified CANDLE burn-up scheme was implemented to create small and long life fast reactors with natural Uranium as fuel cycle input. Such system can utilize natural Uranium resources efficiently without the necessity of enrichment plant or reprocessing plant. The core with metallic fuel based was subdivided into 10 regions with the same volume. The fresh Natural Uranium is initially put in region-1, after one cycle of 10 years of burn-up it is shifted to region-2 and the each region-1 is filled by fresh Natural Uranium fuel. This concept is basically applied to all axial regions. The reactor discharge burn-up is 31.8% HM. From the neutronic point of view, this design is in compliance with good performance

Promotion of uranium enrichment business

International Nuclear Information System (INIS)

Kurushima, Morihiro

1981-01-01

The Committee on Nuclear Power has studied on the basic nuclear power policy, establishing its five subcommittees, entrusted by the Ministry of Nternational Trade and Industry. The results of examination by the subcommittee on uranium enrichment business are given along with a report in this connection by the Committee. In order to establish the nuclear fuel cycle, the aspect of uranium enrichment is essential. The uranium enrichment by centrifugal process has proceeded steadily in Power Reactor and Nuclear Fuel Development Corporation. The following matters are described: the need for domestic uranium enrichment, the outlook for overseas enrichment services and the schedule for establishing domestic enrichment business, the current state of technology development, the position of the prototype enrichment plant, the course to be taken to establish enrichment business the main organization operating the prototype and commercial plants, the system of supplying centrifuges, the domestic conversion of natural uranium the subsidies for uranium enrichment business. (J.P.N.)

LED vs laser fluorimetry: a comparative study for the determination of uranium in natural waters

International Nuclear Information System (INIS)

Shenoy, N.; Parab, H.; Sounderajan, S.; Kiran Kumar; Kumar, S.D.; Reddy, A.V.R.

2015-01-01

Measurement of uranium in water samples has acquired considerable importance ever since its occurrence in drinking water sources was reported. Among the various methods available for uranium quantification at ultra trace levels, laser fluorimetry (LF) method is the method of choice due to its simplicity, speed and high sensitivity compared to other analytical techniques. This technique is based on the measurement of fluorescence of uranium complexes in aqueous solution. Recently, laser source has been replaced by light emitting diode (LEDs) in the fluorimeter systems. In comparison to laser source, LED source is, cost effective, generates less heat and has extended lifetime. Herein, authors have presented a comparison of LED based fluorimeter (Quantalase, Indore, India) and laser fluorimeter (CAT, Indore, India) for the determination of uranium in natural waters

Fluorometric determination of uranium in natural waters

International Nuclear Information System (INIS)

Hues, A.D.; Henicksman, A.L.; Ashley, W.H.; Romero, D.

1977-03-01

Duplicate 200-μl aliquots of the water samples, as received, are transferred by means of Eppendorf pipettors onto 0.4-g pellets of 2 percent LiF-98 percent NaF flux, contained in platinum dishes. The pellets are dried under heat lamps; then fused over special propane burners. The fused pellets are transferred to a Galvanek-Morrison fluorometer, where they are excited with ultraviolet radiation and the fluorescence is measured. The uranium is calculated by comparing the measured fluorescence with that of other pellets, carried through the same procedure, which contain aliquots of standard uranium solutions. The sensitivity of the method is about 0.2 ppB of uranium, and the precision is approximately 15 relative percent in the 0.2- to 10-ppB uranium concentration range

Natural uranium fueled light water moderated breeding hybrid power reactors

International Nuclear Information System (INIS)

Greenspan, E.; Schneider, A.; Misolovin, A.; Gilai, D.; Levin, P.

The feasibility of fission-fusion hybrid reactors based on breeding light water thermal fission systems is investigated. The emphasis is on fuel-self-sufficient (FSS) hybrid power reactors that are fueled with natural uranium. Other LWHRs considered include FSS-LWHRs that are fueled with spent fuel from LWRs, and LWHRs which are to supplement LWRs to provide a tandem LWR-LWHR power economy that is fuel-self-sufficient

Hypertension and hematologic parameters in a community near a uranium processing facility

International Nuclear Information System (INIS)

Wagner, Sara E.; Burch, James B.; Bottai, Matteo; Pinney, Susan M.; Puett, Robin; Porter, Dwayne; Vena, John E.; Hebert, James R.

2010-01-01

Background: Environmental uranium exposure originating as a byproduct of uranium processing can impact human health. The Fernald Feed Materials Production Center functioned as a uranium processing facility from 1951 to 1989, and potential health effects among residents living near this plant were investigated via the Fernald Medical Monitoring Program (FMMP). Methods: Data from 8216 adult FMMP participants were used to test the hypothesis that elevated uranium exposure was associated with indicators of hypertension or changes in hematologic parameters at entry into the program. A cumulative uranium exposure estimate, developed by FMMP investigators, was used to classify exposure. Systolic and diastolic blood pressure and physician diagnoses were used to assess hypertension; and red blood cells, platelets, and white blood cell differential counts were used to characterize hematology. The relationship between uranium exposure and hypertension or hematologic parameters was evaluated using generalized linear models and quantile regression for continuous outcomes, and logistic regression or ordinal logistic regression for categorical outcomes, after adjustment for potential confounding factors. Results: Of 8216 adult FMMP participants 4187 (51%) had low cumulative uranium exposure, 1273 (15%) had moderate exposure, and 2756 (34%) were in the high (>0.50 Sievert) cumulative lifetime uranium exposure category. Participants with elevated uranium exposure had decreased white blood cell and lymphocyte counts and increased eosinophil counts. Female participants with higher uranium exposures had elevated systolic blood pressure compared to women with lower exposures. However, no exposure-related changes were observed in diastolic blood pressure or hypertension diagnoses among female or male participants. Conclusions: Results from this investigation suggest that residents in the vicinity of the Fernald plant with elevated exposure to uranium primarily via inhalation exhibited

Hypertension and hematologic parameters in a community near a uranium processing facility

Energy Technology Data Exchange (ETDEWEB)

Wagner, Sara E., E-mail: swagner@uga.edu [College of Public Health, Department of Epidemiology and Biostatistics, Paul D. Coverdell Center for Biomedical and Health Sciences, University of Georgia, 500 D.W. Brooks Drive, Athens, GA 30602-7396 (United States); Burch, James B. [Arnold School of Public Health, Department of Epidemiology and Biostatistics, University of South Carolina, Columbia, SC (United States); South Carolina Statewide Cancer Prevention and Control Program, Columbia, SC (United States); WJB Dorn Veteran' s Affairs Medical Center, Columbia, SC (United States); Bottai, Matteo [Arnold School of Public Health, Department of Epidemiology and Biostatistics, University of South Carolina, Columbia, SC (United States); Pinney, Susan M. [College of Medicine, Department of Environmental Health, University of Cincinnati, Cincinnati, OH (United States); Puett, Robin [Arnold School of Public Health, Department of Epidemiology and Biostatistics, University of South Carolina, Columbia, SC (United States); South Carolina Statewide Cancer Prevention and Control Program, Columbia, SC (United States); Arnold School of Public Health, Department of Environmental Health Sciences, University of South Carolina, Columbia, SC (United States); Porter, Dwayne [Arnold School of Public Health, Department of Environmental Health Sciences, University of South Carolina, Columbia, SC (United States); Vena, John E. [College of Public Health, Department of Epidemiology and Biostatistics, Paul D. Coverdell Center for Biomedical and Health Sciences, University of Georgia, 500 D.W. Brooks Drive, Athens, GA 30602-7396 (United States); Hebert, James R. [Arnold School of Public Health, Department of Epidemiology and Biostatistics, University of South Carolina, Columbia, SC (United States); South Carolina Statewide Cancer Prevention and Control Program, Columbia, SC (United States)

2010-11-15

Background: Environmental uranium exposure originating as a byproduct of uranium processing can impact human health. The Fernald Feed Materials Production Center functioned as a uranium processing facility from 1951 to 1989, and potential health effects among residents living near this plant were investigated via the Fernald Medical Monitoring Program (FMMP). Methods: Data from 8216 adult FMMP participants were used to test the hypothesis that elevated uranium exposure was associated with indicators of hypertension or changes in hematologic parameters at entry into the program. A cumulative uranium exposure estimate, developed by FMMP investigators, was used to classify exposure. Systolic and diastolic blood pressure and physician diagnoses were used to assess hypertension; and red blood cells, platelets, and white blood cell differential counts were used to characterize hematology. The relationship between uranium exposure and hypertension or hematologic parameters was evaluated using generalized linear models and quantile regression for continuous outcomes, and logistic regression or ordinal logistic regression for categorical outcomes, after adjustment for potential confounding factors. Results: Of 8216 adult FMMP participants 4187 (51%) had low cumulative uranium exposure, 1273 (15%) had moderate exposure, and 2756 (34%) were in the high (>0.50 Sievert) cumulative lifetime uranium exposure category. Participants with elevated uranium exposure had decreased white blood cell and lymphocyte counts and increased eosinophil counts. Female participants with higher uranium exposures had elevated systolic blood pressure compared to women with lower exposures. However, no exposure-related changes were observed in diastolic blood pressure or hypertension diagnoses among female or male participants. Conclusions: Results from this investigation suggest that residents in the vicinity of the Fernald plant with elevated exposure to uranium primarily via inhalation exhibited

Uranium mining and processing: their radiation impact into the environment

International Nuclear Information System (INIS)

Ostapczuk, Peter; Zoriy, Petro; Dederichs, Herbert; Lennartz, Reinhard

2008-01-01

Based on Thorium and Uranium determination in soil and plants samples collected in the region of Aktau, Kazakhstan the distribution pattern of environmental pollution by these elements was correlated with the radiation dose. The main radiation source was the waste deposit of the equipment used by the uranium processing (dose higher than 5 μSv/h). The mining area and also the transportation way from mine to the uranium factory has also an radiation impact which is difficult to estimate. Based on the data found by plants and soil samples all the area under study has a higher pollution level by Thorium and Uranium than the control area (about 0.1μSv/h). Due to observed strong wind blowing in different directions it is possible that the particle of uranium ore has been transported for long distance and polluted the plants and upper soil layer. The further investigations should get more information about this supposition. (author)

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

International Nuclear Information System (INIS)

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

2010-01-01

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

Process for recovering uranium using an alkyl pyrophosphoric acid and alkaline stripping solution

International Nuclear Information System (INIS)

Worthington, R.E.; Magdics, A.

1987-01-01

A process is described for stripping uranium for a pregnant organic extractant comprising an alkyl pyrophosphoric acid dissolved in a substantially water-immiscible organic diluent. The organic extractant contains tetravalent uranium and an alcohol or phenol modifier in a quantity sufficient to retain substantially all the unhydrolyzed alkyl pyrophosphoric acid in solution in the diluent during stripping. The process comprises adding an oxidizing agent to the organic extractant and thereby oxidizing the tetravalent uranium to the +6 state in the organic extractant, and contacting the organic extractant containing the uranium in the +6 state with a stripping solution comprising an aqueous solution of an alkali metal or ammonium carbonate or hydroxide thereby stripping uranium from the organic extractant into the stripping solution. The resulting barren organic extractant containing substantially all of the unhydrolyzed alkyl pyrophosphoric acid dissolved in the diluent is separated from the stripping solution containing the stripped uranium, the barren extractant being suitable for recycle

Smectite-zeolite envelope surrounding the Tsukiyoshi uranium deposit, central Japan. A natural analogue study

International Nuclear Information System (INIS)

Utada, Minoru

2003-01-01

The Tsukiyoshi uranium deposit in Gifu Prefecture is the largest one in Japan. It is embedded in lower part of the Mizunami Group of Miocene age. Relating to the existence of this uranium deposit, the constituent minerals in sediments were studied by XRD and SEM, using many drilling cores. The most abundant authigenic mineral is smectite. The amount of smectite increases generally from upper to lower horizons, and a highly smectitized zone is situated around the uranium deposit. Smectitization predominated in mafic glassy grains of sediments, which was probably formed in early burial diagenesis. Zeolites including clinoptilolite-heulandite, mordenite, analcime, chabazite and philipsite are secondly abundant authigenic minerals. They seem to have been formed at early to late diagenetic stages. Opaline silica is rather rare. Carbonate minerals, including calcite, dolomite, siderite and rhodocrosite are common. They may be formed by diagenesis as well. Gypsum and pyrite occur in upper horizons and lower horizons, respectively. In particular, a highly smectitized zone including pyrite probably played an important role for retarding the migration of uranium and as a result keeping the uranium deposit for past one million years. This smectite-zeolite envelope surrounding the Tsukiyoshi uranium deposit is regarded as a natural analogue of the buffer materials surrounding the high-level radioactive waste repository. (author)

Uranium

International Nuclear Information System (INIS)

1982-01-01

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

On the nature of the phase transition in uranium dioxide

Science.gov (United States)

Gofryk, K.; Mast, D.; Antonio, D.; Shrestha, K.; Andersson, D.; Stanek, C.; Jaime, M.

Uranium dioxide (UO2) is by far the most studied actinide material as it is a primary fuel used in light water nuclear reactors. Its thermal and magnetic properties remain, however, a puzzle resulting from strong couplings between magnetism and lattice vibrations. UO2 crystalizes in the face-centered-cubic fluorite structure and is a Mott-Hubbard insulator with well-localized uranium 5 f-electrons. In addition, below 30 K, a long range antiferromagnetic ordering of the electric-quadrupole of the uranium moments is observed, forming complex non-collinear 3-k magnetic structure. This transition is accompanied by Jahn-Teller distortion of oxygen atoms. It is believed that the first order nature of the transition results from the competition between the exchange interaction and the Jahn-Teller distortion. Here we present results of our extensive thermodynamic investigations on well-characterized and oriented single crystals of UO2+x (x = 0, 0.033, 0.04, and 0.11). By focusing on the transition region under applied magnetic field we are able to study the interplay between different competing interactions (structural, magnetic, and electrical), its dynamics, and relationship to the oxygen content. We will discuss implications of these results. Work supported by the Department of Energy, Office of Basic Energy Sciences, Materials Sciences, and Engineering Division.

Oxidizing attack process of uranium ore by a carbonated liquor

International Nuclear Information System (INIS)

Maurel, Pierre; Nicolas, Francois.

1981-01-01

A continuous process for digesting a uraniferous ore by oxidation with a recycling aqueous liquor containing alkaline carbonates and bicarbonates in solution as well as uranium in a concentration close to its solubility limit at digestion temperature, and of recuperation of the precipitated uranium within the solid phase remaining after digestion. The digestion is carried out by spraying oxygen into the hot reactional medium in order not only to permit oxidation of the uranium and its solubilization but also to ensure that the sulphides of impurities and organic substances present in the ore are oxidized [fr

Extraction and desorption of accessible uranium

International Nuclear Information System (INIS)

Payne, T.

1987-01-01

The proportion of the uranium in natural ore samples which is in isotopic equilibrium with the uranium in the groundwater may be designated accessible uranium, and can be regarded as being in short-term exchange with the aqueous phase. Some of the natural uranium is secured in resistant crystalline minerals, and is described as inaccessible, because it may not be brought into solution unless the mineral is subjected to extreme chemical attack. It is not available for groundwater transport in the short term. An estimate of the proportion of accessible uranium is therefore useful when modeling radionuclide migration. The amount of accessible natural uranium is some uranium ore samples from the Ranger deposit has been determined by combining a sequential extraction with isotopic measurements of the extracted phases. The solid samples were crushed drill core form Ranger S1/146 which had previously been used for uranium adsorption experiments and therefore contained 236 U as well as natural uranium. This Section discusses how the uranium partitioning found with the sequential extraction procedure predicts the leaching behavior of these samples

The fluorimetry for control of internal contamination of exposed workers to natural and enriched uranium; A fluorimetria para o controle da contaminacao interna dos trabalhadores expostos a uranio natural e enriquecido

Energy Technology Data Exchange (ETDEWEB)

Gaburo, J.C.; Todo, A.S.; Sordi, G.M.A.A. [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil)]. E-mail: janetegc@net.ipen.br

2000-07-01

This study is a part of bioassay program revision applied to the uranium processing plants at IPEN-CNEN/SP. The workers of these facilities handle both natural uranium and uranium compounds with different isotopic composition which could reach up to 20% in 235 U. The most commonly employed techniques for the determination of uranium in urine at IPEN are fluorimetry and alpha spectrometry with detection limit of 1.0 mgL-1. and 1,0 mBqL-1 , respectively. Based in advantages and disadvantages of each technique it is very important to identify the workers groups that should be submitted for these analysis. In this report a limiting value of uranium concentration in urine, mgL-1, obtained by fluorimetry is proposed. All the results greater than these limiting value indicate the necessity to carry out a additional measurement by alpha spectroscopy. The uranium mass that result in a pre-determined limit committed effective dose is function of isotopic composition. Consequently, the predicted value of the measured of urinary excretion is function of isotopic composition also and depends of absorption characteristics when inhaled and of the monitoring interval considered. In this report the uranium concentration values for reference levels and limits doses are determined. Based on these results the procedures to use the fluorimetry or both fluorimetry and alpha-spectrometry were adopted. (author)

Bicarbonate Elution of Uranium from Amidoxime-Based Polymer Adsorbents for Sequestering Uranium from Seawater

Energy Technology Data Exchange (ETDEWEB)

Pan, Horng-Bin [Department of Chemistry, University of Idaho, Moscow, Idaho 83844 USA; Wai, Chien M. [Department of Chemistry, University of Idaho, Moscow, Idaho 83844 USA; Kuo, Li-Jung [Pacific Northwest National Laboratory, Marine Sciences Laboratory, Sequim, Washington 98382 USA; Gill, Gary [Pacific Northwest National Laboratory, Marine Sciences Laboratory, Sequim, Washington 98382 USA; Tian, Guoxin [Lawrence Berkeley National Laboratory, Berkeley, California 94720 USA; Rao, Linfeng [Lawrence Berkeley National Laboratory, Berkeley, California 94720 USA; Das, Sadananda [Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 USA; Mayes, Richard T. [Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 USA; Janke, Christopher J. [Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831 USA

2017-05-02

Uranium adsorbed on amidoxime-based polyethylene fibers in simulated seawater can be quantitatively eluted using 3 M KHCO3 at 40°C. Thermodynamic calculations are in agreement with the experimental observation that at high bicarbonate concentrations (3 M) uranyl ions bound to amidoxime molecules are converted to uranyl tris-carbonato complex in the aqueous solution. The elution process is basically the reverse reaction of the uranium adsorption process which occurs at a very low bicarbonate concentration (~10-3 M) in seawater. In real seawater experiments, the bicarbonate elution is followed by a NaOH treatment to remove natural organic matter adsorbed on the polymer adsorbent. Using the sequential bicarbonate and NaOH elution, the adsorbent is reusable after rinsing with deionized water and the recycled adsorbent shows no loss of uranium loading capacity based on real seawater experiments.

Determination of natural uranium, thorium and radium isotopes in water and soil samples by alpha spectroscopy

Energy Technology Data Exchange (ETDEWEB)

Hao, Le Cong; Tao, Chau Van; Thong, Luong Van; Linh, Duong Mong [University of Science Ho Chi Minh City (Viet Nam). Faculty of Physics and Engineering Physics; Dong, Nguyen Van [University of Science Ho Chi Minh City (Viet Nam). Faculty of Chemistry

2011-08-15

In this study, a simple procedure for the determination of natural uranium, thorium and radium isotopes in water and soil samples by alpha spectroscopy is described. This procedure allows a sequential extraction polonium, uranium, thorium and radium radionuclides from the same sample in two to three days. It was tested and validated with the analysis of certified reference materials from the IAEA. (orig.)

Rapid determination of uranium in natural waters by fthermal emission mass spectrometry

International Nuclear Information System (INIS)

Ferguson, J.R.; Caylor, J.D.; Rogers, E.R.; Cole, S.H.

1977-03-01

A method has been developed to rapidly analyze natural water samples for part-per-trillion (ng/l) concentrations of uranium using a custom-built thermal-emission mass spectrometer. The filtered water sample is spiked with 233 U as an internal standard and extracted with a 2 percent solution of TOPO (trioctylphosphine oxide) in carbon tetrachloride. An aliquot of the organic phase is evaporated and the uranium in the residue extracted with aqueous ammonium carbonate. A 5j-μl aliquot is taken and dried on a flat uranium concentration of 3 ng/l will yield a count rate greater than three times the standard deviation, plus the mean of the background, and is defined as the lowest determinable concentration. The standard deviation of the method is 3 percent at accuracy of the method has been evaluated by comparing the results with a fluorescence procedure. There is very good agreement for water samples with uranium concentrations from 200 to 1000 ng/l. The mass spectrometer is a 6-in. -radius, 60-degree-sector instrument equipped for ion counting and having a vacuum system allowing rapid sample changing while maintaining a high source vacuum. A multiplexer and high-voltage s witch provide synchronized peak switching and scaler gating for monitoring three isotopes of uranium 238, 235, and 233. With this instrument, an analyst can achieve an analysis rate in excess of 50 samples per eight-hour shift

The chemical industry of uranium in France; L'industrie chimique de l'uranium en France

Energy Technology Data Exchange (ETDEWEB)

Goldschmidt, B [Commissariat a l' Energie Atomique, Paris (France). Centre d' Etudes Nucleaires

1955-07-01

The actual CEA program is concerned with the construction of two large graphite reactors, each of those containing at least one hundred tons of uranium metal with nuclear purity. The uranium for these two reactors will be regularly supplied by new resources discovered in France and Madagascar in the last five years. The working and treatment of such ore have led to the creation of an important french industry of which the general outline and principle are described. The operated ores have got different natures and concentration, individual characteristics are described for the main ores.The most high-grade ore are transported to a central plant in Bouchet near Paris; the low-grade ore are concentrated by physical methods or chemical processes of which principles and economy are studied with constancy. The acid processes are the only used until now, although the carbonated alkaline processes has been studied in France. The next following steps after the acid process until the obtention of uranium rich concentrate are described. The purification steps of uranium compounds to nuclear purity material are described as well as the steps to elaborate metal of which the purity grade will be specify. Finally, the economic aspects of uranium production difficulty will be considered in relation with technical progresses which we can expect to achieve in the future. (M.P.)

The future of the uranium mining industry

International Nuclear Information System (INIS)

Capus, G.; Galaud, G.

1993-01-01

This paper presents the state of natural Uranium market today. In a first part, the author gives a brief history about nuclear programs history in Usa and Europe and describes natural Uranium demand and supply (Uranium mines, recycling, excessive civil stocks, military stocks using). In a second part, evolutions and futures of Uranium industry is studied: using of excessive stocks in Western Europe, using of military stocks, recycling of Uranium from spent fuels reprocessing, uranium deposits, future natural uranium market. 6 refs., 4 figs., 3 tabs., 3 photos

Uranium, depleted uranium, biological effects

International Nuclear Information System (INIS)

2001-01-01

Physicists, chemists and biologists at the CEA are developing scientific programs on the properties and uses of ionizing radiation. Since the CEA was created in 1945, a great deal of research has been carried out on the properties of natural, enriched and depleted uranium in cooperation with university laboratories and CNRS. There is a great deal of available data about uranium; thousands of analyses have been published in international reviews over more than 40 years. This presentation on uranium is a very brief summary of all these studies. (author)

Development of a stable uranium recovery regulatory framework for uranium recovery activities in the United States

International Nuclear Information System (INIS)

Layton, M.C.; Abrams, C.E.

2000-01-01

The U.S. Nuclear Regulatory Commission (NRC) has historically regulated operations at all uranium and thorium recovery facilities under the authority of the Atomic Energy Act of 1954, as amended. Uranium recovery facilities are those plants, or portions of facilities that process uranium- or thorium-bearing material primarily for its source material content. The uranium recovery industry expressed some concerns over several aspects of the NRC's practices, as described in the NRC's guidance documents. In April 1998, the National Mining Association submitted a report to the Commission, that identified specific concerns with NRC's current position and guidance regarding concurrent jurisdiction at uranium mills; dual regulatory authority at in situ leach facilities; the use of mill tailings impoundments for disposal of radioactive material other than 11e.(2) byproduct material; and the ability to process alternate feed material at uranium mills. The NRC staff addressed most of these concerns in two SECY (staff recommendations) papers that were concurrently provided to the Commission, along with a SECY paper on a draft rulemaking plan relating to these and other issues. The issues addressed in these papers included a new rulemaking, disposal of materials other than 11 e.(2) byproduct material, processing of materials other than natural ores, and improved efficiency for regulating in situ leach uranium facilities. The Commission issued final policy decisions on these issues and directions for NRC staff to implement those decisions in July 2000. (author)

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

International Nuclear Information System (INIS)

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

1983-01-01

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

Spontaneous ignition of natural uranium in Tokai Research Establishment, Japan Atomic Energy Research Institute

International Nuclear Information System (INIS)

1989-01-01

At P.M. 7:23, May 30, 1989, a fire alarm functioned in the uranium enrichment laboratory building, and immediately investigation was carried out, as the result, smoke was confirmed in the nuclear fuel storage. In the nuclear fuel storage, there were five plastic bottles containing natural uranium chips, and smoke arose from three of them. Immediately fire fighting was carried out with powder extinguishers and others, the uranium chips which were regarded as the heat generating source were moved into stainless steel cans, and air was cut off with extinguishing sand, as the result, around P.M. 9:50, heat generation ceased. At present the detailed cause is being investigated, but it is considered that the uranium chips contained in plastic bottles reacted with air by some cause, and generated heat in the form of spontaneous ignition, as the result, the plastic bottles and the vinyl sheets placed under them smoked. The stack dust monitor in the uranium enrichment laboratory building showed the normal value, and there was not the effect to surrounding environment. The workers who did fire fighting with whole face masks were not affected by smoke. (K.I.)

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

Energy Technology Data Exchange (ETDEWEB)

Silva Neto, Joao Batista da

2008-07-01

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

76 FR 60941 - Policy Regarding Submittal of Amendments for Processing of Equivalent Feed at Licensed Uranium...

Science.gov (United States)

2011-09-30

... Processing of Equivalent Feed at Licensed Uranium Recovery Facilities AGENCY: Nuclear Regulatory Commission... State-licensed uranium recovery site, either conventional, heap leach, or in situ recovery. DATES... Regarding Submittal of Amendments for Processing of Equivalent Feed at Licensed Uranium Recovery Facilities...

Developments in natural uranium - graphite reactors; Developpement des reacteurs a graphite et uranium naturel

Energy Technology Data Exchange (ETDEWEB)

Bourgeois, J. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires; Saitcevsky, B. [Electricite de France (EDF), 75 - Paris (France)

1964-07-01

The French natural uranium-graphite power-reactor programme has been developing - from EDF 1 to EDF 4 - in the direction of an increase of the unit power of the installations, of the specific and volume powers, and of an improvement in the operational security conditions. The high power of EDF 4 (500 MWe) and the integration of the primary circuit into the reactor vessel, which is itself made of pre-stressed concrete, make it possible to make the most of the annular fuel elements already in use in EDF 1, and to arrive thus at a very satisfactory solution. The use of an internally cooled fuel element (an annular element) has led to a further step forward: it now becomes possible to increase the pressure of the cooling gas without danger of causing creep in the uranium tube. The use of a pre-stressed concrete vessel makes this pressure increase possible, and the integration of the primary circuit avoids the risk of a rapid depressurization which would be in this case a major danger. This report deals with the main problems presented by this new type of nuclear power station, and gives the main lines of research and studies now being carried out in France. - Neutronic and thermal research has made it possible to consider using large size fuel elements (internal diameter = 77 mm, external diameter 95 mm) while still using natural uranium. - The problems connected with the production of these elements and with their in pile behaviour are the subject of a large programme, both out of pile and in power reactors (EDF 2) and test reactors (Pegase). - The increase in the size of the element leads to a large lattice pitch (35 to 40 cm). This makes it possible to consider having one charging aperture per channel or for a small number of channels, whether the charge machine be inside or outside the pressure vessel. In conclusion are given the main characteristics of a project for a 500 MWe power station using such a fuel element. In particular this project is compared to EDF 4

The jet nozzle process for uranium 235 isotopic enrichment

International Nuclear Information System (INIS)

Jordan, I.; Umeda, K.; Brown, A.E.P.

1979-01-01

A general survey of the isotopic enrichment of Uranium - 235, principally by jet nozzle process, is made. Theoretical treatment of a single stage and cascade of separation stages of the above process with its development in Germany until 1976 is presented [pt

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.

Study on the chemical treatment processes of the uranium pyrochlore of Araxa

International Nuclear Information System (INIS)

Batista, H.F.; Fernandes, M.D.

Several processes are presented for the chemical treatment, in laboratory scale, of the uranium pyrochlore concentrates found in Araxa (Minas Gerais, Brazil), aiming to the extraction of uranium, thorium and rare earths, besides the recovery of niobium pentoxide [pt

Machining of uranium and uranium alloys

International Nuclear Information System (INIS)

Morris, T.O.

1981-01-01

Uranium and uranium alloys can be readily machined by conventional methods in the standard machine shop when proper safety and operating techniques are used. Material properties that affect machining processes and recommended machining parameters are discussed. Safety procedures and precautions necessary in machining uranium and uranium alloys are also covered. 30 figures

Development of Practical Remediation Process for Uranium-Contaminated Concrete

Energy Technology Data Exchange (ETDEWEB)

Kim, S. S.; Kim, W. S.; Kim, G. N.; Moon, J. K. [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2013-10-15

A volume reduction of the concrete waste by the appropriate treatment technologies will decrease the amount of waste to be disposed of and result in a reduction of the disposal cost and an enhancement of the efficiency of the disposal site. Our group has developed a 100 drums/year decontamination process and facilities for the decontamination of radioactive concrete. This practical scale process is little known. A practical decontamination process was developed to remove uranium from concrete pieces generated from the decommissioning of a uranium conversion plant. The concrete pieces are divided into two groups: concrete coated with and without epoxy. For the removal of epoxy from the concrete, direct burning by an oil flame is preferable to an electric heating method. The concrete blocks are crushed to below 30 mm and sifted to 1 mm. When the concrete pieces larger than 1 mm are sequentially washed with a clear washing solution and 1.0 M of nitric acid, most of their radioactivity reaches below the limit value of uranium for self-disposal. The concrete pieces smaller than 1 mm are decontaminated in a rotary washing machine by nitric acid, and an electrokinetic equipment is also used if their radioactivity is high.

Development of Practical Remediation Process for Uranium-Contaminated Concrete

International Nuclear Information System (INIS)

Kim, S. S.; Kim, W. S.; Kim, G. N.; Moon, J. K.

2013-01-01

A volume reduction of the concrete waste by the appropriate treatment technologies will decrease the amount of waste to be disposed of and result in a reduction of the disposal cost and an enhancement of the efficiency of the disposal site. Our group has developed a 100 drums/year decontamination process and facilities for the decontamination of radioactive concrete. This practical scale process is little known. A practical decontamination process was developed to remove uranium from concrete pieces generated from the decommissioning of a uranium conversion plant. The concrete pieces are divided into two groups: concrete coated with and without epoxy. For the removal of epoxy from the concrete, direct burning by an oil flame is preferable to an electric heating method. The concrete blocks are crushed to below 30 mm and sifted to 1 mm. When the concrete pieces larger than 1 mm are sequentially washed with a clear washing solution and 1.0 M of nitric acid, most of their radioactivity reaches below the limit value of uranium for self-disposal. The concrete pieces smaller than 1 mm are decontaminated in a rotary washing machine by nitric acid, and an electrokinetic equipment is also used if their radioactivity is high

Uranium in Nova Scotia: a background summary for the uranium inquiry, Nova Scotia

International Nuclear Information System (INIS)

1982-01-01

Since the mid 1970's Nova Scotia has experienced increased exploration for a number of commodities including uranium. The exploration activity for uranium has resulted in discovery of significant occurrences of the element. It became obvious to the Government of Nova Scotia that a segment of the population of the Province is concerned about the potential hazards associated with the exploration, mining and milling stages of the uranium industry. Public concern has resulted in the appointment of a Commissioner under the Public Inquiries Act of Nova Scotia to inquire and make recommendations to the Governor-in-Council on all aspects of exploration, development, mining, processing, storage, waste management and transportation of uranium in any form. The regulation of mineral exploration and mining activities is carried out by the Nova Scotia Department of Mines and Energy through the Mineral Resources Act of the Province of Nova Scotia. The regulation of the special radioactive aspects involved in the mining and processing of uranium ore is the responsibility of the federal Atomic Energy Control Board. The purposes of this report is to: outline the history of uranium exploration in Nova Scotia; summarize the results of geological surveys by provincial and federal government agencies, universities and exploration companies which document the natural levels of radioactivity in the Province; briefly outline the physical and chemical characteristics of uranium and thorium which make these elements unique and a potential environmental and health concern; outline chronologically the steps taken by the Nova Scotia Department of Mines and Energy to monitor and regulate uranium exploration activities; classify the types of uranium deposits known to occur in Nova Scotia and describe their main geological features; outline the role of the Nova Scotia Department of Mines and Energy in the regulation of mining activities in the Province. The report is written for the interested

Natural and depleted uranium in the topsoil of Qatar: Is it something to worry about?

International Nuclear Information System (INIS)

Shomar, Basem; Amr, Mohamed; Al-Saad, Khalid; Mohieldeen, Yasir

2013-01-01

Highlights: • Scientific studies on Uranium in the arid environment are almost absent. • Qatar is closed to Iraq and Iran where the two countries were exposed to long wars. • The paper introduces baseline study integrates chemistry, instrumentation and GIS mapping. • The study opens new horizons for similar studies on the field using similar approach. - Abstract: This study examines uranium in soils of Qatar to investigate whether there is any detectable traces of depleted uranium (DU). 409 soil samples were collected using a 10 km grid system throughout the State of Qatar. The U concentrations and isotopic compositions ( 235 U/ 238 U) were determined using an ICP-MS. The U concentrations range from 0.05 to 4.7 mg/kg and the 235 U/ 238 U isotopic signatures are in the range 0.007–0.008, i.e. comparable to the isotopic ratio in natural uranium (NU). The distribution of these concentrations in the topsoil were used to see correlations with locations of pollution point sources and environmentally hot areas associated with human activity: industrial estates, solid waste dumping sites, wastewater treatment plants, sea harbors, airports, and public transport network. New thematic maps were built using Geographic Information System (GIS) software. The results showed that there is no linkage between the occurrence, distribution, concentrations and isotopic ratios of U and these hotspots. More importantly, due to the low concentration of organic matter (OM) in soils of Qatar, very limited P-fertilization, the alkaline nature of soil (pH 8) and low Fe/Mn contents make soil uranium concentrations very low. The residential areas, including the capital Doha, had the lowest total concentrations of uranium and isotopic ratios of the country while the northern and western parts showed the highest values

Uranium and sulphate values from carbonate leach process

International Nuclear Information System (INIS)

Berger, B.

1983-01-01

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

Process water treatment at the Ranger uranium mine, Northern Australia.

Science.gov (United States)

Topp, H; Russell, H; Davidson, J; Jones, D; Levy, V; Gilderdale, M; Davis, S; Ring, R; Conway, G; Macintosh, P; Sertorio, L

2003-01-01

The conceptual development and piloting of an innovative water treatment system for process water produced by a uranium mine mill is described. The process incorporates lime/CO2 softening (Stage 1), reverse osmosis (Stage 2) and biopolishing (Stage 3) to produce water of quality suitable for release to the receiving environment. Comprehensive performance data are presented for each stage. The unique features of the proposed process are: recycling of the lime/CO2 softening sludge to the uranium mill as a neutralant, the use of power station off-gas for carbonation, the use of residual ammonia as the pH buffer in carbonation; and the recovery and recycling of ammonia from the RO reject stream.

Maintenance of a labour safety and ecological safety in chinks at extraction of uranium

International Nuclear Information System (INIS)

Svambaev, Z.A.; Svambaev, E.A.; Sultanbekov, G.A; Tusupbekova, S.T.; Svambaev, A.S.

2010-01-01

The authors of scientific work inform results of research on maintenance of a labour safety and ecological safety in chinks at extraction of uranium. Practical actions on increase of safety and a labour safety in chinks at extraction of uranium in opinion of the author is the practical actions directed on perfection of technological processes, development of means of the control and management of technological processes, modernization of the equipment, the organization of safe workplaces of the personnel. It is necessary to give significant attention to actions connected with improvement of physical protection of radioactive dangerous objects. The basic radiating, toxicological danger at the enterprises underground extractions of uranium are natural atoms uranium - the thorium lines, contained in technological solutions, in finished goods, in radioactive waste products, on a surface of the process equipment, vehicles and packings. In manufacture of uranium use highly toxic substances, such as the concentrated sulfuric acid, hydrogen H 2 O 2 , ammonia water with maintenance - not less than 25 %. The technological circuit of reception sour - oxide natural uranium is represented in the following. The solutions acting from uterus sobered after sedimentation from mechanical impurity and after clarification moves in technical unit sonar where it is possible a sulfuric acid and submit through pump down chinks under pressure to uranium horizon where the productive solution of uranium is formed. The productive solution of uranium with the help of deep pumps through pump out chinks acts on unit of reception of a productive solution, then in modular capacity where there is a process clarification, his ambassador moves on sobered to extraction of uranium that is for processing. On a processing complex the productive solution from modular capacity acts on sobered columns in them occurs sobered uranium from a productive solution on ion exchange pitches or so the sorbent, and

Status report from USSR [Processing of Low-Grade Uranium Ores]; Doklad o sostoyanii voprosa v SSSR

Energy Technology Data Exchange (ETDEWEB)

Zefirov, A P [Gosudarstvennyj Komitet Po Ispol' zovaniyu Atomnoj Ehnergii SSSR, Moskva, Union of Soviet Socialist Republics (Russian Federation)

1967-06-15

The uranium industry for processing poor uranium ores in the USSR was established in recent years. As a result of research work institutions and enterprises in the development of this industry was provided by rapid technological advances that allowed dramatically increased productivity, reduced consumption of reagents, simplified process flow diagrams, and reduced production costs. At present, the basis for uranium industry, including and poor uranium ore deposits in the USSR are with different content valuable components (uranium, phosphorus, molybdenum, rare earth elements, thorium, iron, .. .)

Adsorption of dissolved uranium from well water. Part I

International Nuclear Information System (INIS)

Jasper, S.; Oldham, W.K.

1982-01-01

This study was undertaken in response to a request from the provincial Ministry of Health, to evaluate several methods for removal of uranium from well water in the Okanagan Valley of British Columbia. The naturally occurring uranium levels in some of these wells is above 100 ppb, and as the drinking water standard for uranium is 20 ppb, it has become necessary to develop an efficient, easily operated system to reduce uranium concentration. This study comprises the first step in this process by selecting the most appropriate adsorbent and estimating its efficiency and capacity

Process for in-situ leaching of uranium

International Nuclear Information System (INIS)

Espenscheid, W.F.; Yan, F.Y.

1983-01-01

The present invention relates to the recovery of uranium from subterranean ore deposits, and more particularly to an in-situ leaching operation employing an aqueous solution of sulfuric acid and carbon dioxide as the lixiviant. Uranium is solubilized in the lixiviant as it traverses the subterranean uranium deposit. The lixiviant is subsequently recovered and treated to remove the uranium

Calculations on heavy-water moderated and cooled natural uranium fuelled power reactors

International Nuclear Information System (INIS)

Pinedo V, J.L.

1979-01-01

One of the codes that the Instituto Nacional de Investigaciones Nucleares (Mexico) has for the nuclear reactors design calculations is the LEOPARD code. This work studies the reliability of this code in reactors design calculations which component materials are the same of the heavy water moderated and cooled, natural uranium fuelled power reactors. (author)

The manufacturing of depleted uranium biological shield components

International Nuclear Information System (INIS)

Metelkin, J.A.

1998-01-01

The unique combination of the physical and mechanical properties of uranium made it possible to manufacture biological shield components of transport package container (TPC) for transportation nuclear power plant irradiated fuel and radionuclides of radiation diagnostic instruments. Protective properties are substantially dependent on the nature radionuclide composition of uranium, that why I recommended depleted uranium after radiation chemical processing. Depleted uranium biological shield (DUBS) has improved specific mass-size characteristics compared to a shield made of lead, steel or tungsten. Technological achievements in uranium casting and machining made it possible to manufacture DUBS components of TPC up to 3 tons of mass and up to 2 metres of the maximum size. (authors)

Improving the Assessment of Internal Occupational Exposure to Natural Uranium from Urinalysis by Normalization to Creatinine

International Nuclear Information System (INIS)

Marko, R.; Kol, R.; Katorza, E.; German, U.; Balaish, Y.; Lorber, A.; Karpas, Z.

2002-01-01

The assessment of occupational internal exposure to natural uranium is normally carried out by combining Uranium Lung Detection (ULD) and urine analysis. The ULD is a direct measurement of the uranium content in lungs. The urine analysis measures the amount of uranium excreted from the body. The biokinetic models that are in use for dose assessments from urine analysis measurements are usually based on 24-hour urine collection. There are three traditional methods to collect urine samples: a) 24-hour collection - the subject is asked to collect all the urine excreted during a 24-hour period. b) Simulated 24-hour collection - the subject collects all the urine excreted during three consecutive 8-hour workdays. c) Spot samples - the subject gives a single urine sample at some time during work hours

Process for winning uranium from wet process phosphoric acid

International Nuclear Information System (INIS)

1980-01-01

A process is described for winning uranium from wet process phosphoric acid by means of liquid-liquid extraction with organic phosphoric acid esters. The process is optimised by keeping the sulphate percentage in the phosphoric acid below 2% by weight, and preferably below 0.6% by weight, as compared to P 2 O 5 in the phosphoric acid. This is achieved by adding an excess of Ba and/or Ca carbonate or sulfide solution and filtering off the formed calcium and/or barium sulphate precipitates. Solid KClO 3 is then added to the filtrate to oxidise U 4+ to U 6+ . The normal extraction procedure using organic phosphoric esters as extraction liquid, can then be applied. (Th.P.)

Uranium and plutonium in marine sediments

International Nuclear Information System (INIS)

Ordonez R, E.; Almazan T, M. G.; Ruiz F, A. C.

2011-11-01

The marine sediments contain uranium concentrations that are considered normal, since the seawater contains dissolved natural uranium that is deposited in the bed sea in form of sediments by physical-chemistry and bio-genetics processes. Since the natural uranium is constituted of several isotopes, the analysis of the isotopic relationship 234 U/ 238 U are an indicator of the oceanic activity that goes accumulating slowly leaving a historical registration of the marine events through the profile of the marine soil. But the uranium is not the only radioelement present in the marine sediments. In the most superficial strata the presence of the 239+140 Pu has been detected that it is an alpha emitter and that recently it has been detected with more frequency in some coasts of the world. The Mexican coast has not been the exception to this phenomenon and in this work the presence of 239-140 Pu is shown in the more superficial layers of an exploring coming from the Gulf of Tehuantepec. (Author)

In situ leaching process for recording uranium values

International Nuclear Information System (INIS)

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

1977-01-01

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

Geochemical behaviour of uranium in sedimentary formations: insights from a natural analogue study - 16340

International Nuclear Information System (INIS)

Noseck, Ulrich; Brasser, Thomas; Havlova, Vaclava; Cervinka, Radek; Suksi, Juhani

2009-01-01

Groundwater data from the natural analogue site Ruprechtov have been evaluated with special emphasis on the uranium behaviour in the so-called uranium-rich clay/lignite horizon. In this horizon in-situ Eh-values in the range of -160 to -280 mV seem to be determined by the SO 4 2- /HS - couple. Under these conditions U(IV) is expected to be the preferential redox state in solution. However, on-site measurements in groundwater from the clay/lignite horizon show only a fraction of about 20 % occurring in the reduced state U(IV). Thermodynamic calculations reveal that the high CO 2 partial pressure in the clay/lignite horizon can stabilise hexavalent uranium, which explains the occurrence of U(VI). The calculations also indicate that the low uranium concentrations in the range between 0.2 and 2.1 μg/l are controlled by amorphous UO 2 and/or the U(IV) phosphate mineral ningyoite. This confirms the findings from previous work that the uranium (IV) mineral phases are long-term stable under the reducing conditions in the clay/lignite horizon without any signatures for uranium mobilisation. It supports the current knowledge of the geological development of the site and is also another important indication for the long-term stability of the sedimentary system itself, namely of the reducing geochemical conditions in the near-surface (30 m to 60 m deep) clay/lignite horizon. Further work with respect to the impact of changes in redox conditions on the uranium speciation is on the way. (authors)

Metabolomics identifies a biological response to chronic low-dose natural uranium contamination in urine samples.

Science.gov (United States)

Grison, Stéphane; Favé, Gaëlle; Maillot, Matthieu; Manens, Line; Delissen, Olivia; Blanchardon, Eric; Banzet, Nathalie; Defoort, Catherine; Bott, Romain; Dublineau, Isabelle; Aigueperse, Jocelyne; Gourmelon, Patrick; Martin, Jean-Charles; Souidi, Maâmar

2013-01-01

Because uranium is a natural element present in the earth's crust, the population may be chronically exposed to low doses of it through drinking water. Additionally, the military and civil uses of uranium can also lead to environmental dispersion that can result in high or low doses of acute or chronic exposure. Recent experimental data suggest this might lead to relatively innocuous biological reactions. The aim of this study was to assess the biological changes in rats caused by ingestion of natural uranium in drinking water with a mean daily intake of 2.7 mg/kg for 9 months and to identify potential biomarkers related to such a contamination. Subsequently, we observed no pathology and standard clinical tests were unable to distinguish between treated and untreated animals. Conversely, LC-MS metabolomics identified urine as an appropriate biofluid for discriminating the experimental groups. Of the 1,376 features detected in urine, the most discriminant were metabolites involved in tryptophan, nicotinate, and nicotinamide metabolic pathways. In particular, N -methylnicotinamide, which was found at a level seven times higher in untreated than in contaminated rats, had the greatest discriminating power. These novel results establish a proof of principle for using metabolomics to address chronic low-dose uranium contamination. They open interesting perspectives for understanding the underlying biological mechanisms and designing a diagnostic test of exposure.

Improvements on heap leaching process for a refractory uranium ore and yellow cake precipitation process

International Nuclear Information System (INIS)

Feng Jianke

2013-01-01

Some problems such as formed harden matrix, ore heap compaction, poor permeability, and agglomeration of absorption resin occur during extracting uranium from a refractory uranium ore by heap leaching process. After some measures were taken, i.e. spraying a new ore heap by low concentration acid, two or more ore heaps in series leaching, turning ores in ore heap, the permeability was improved, acid consumption was reduced. Through precipitate circulation and aging, the yellow cake slurry in amorphous or microlite form was transformed to crystal precipitate, thus uranium content in yellow cake was improved, and water content in yellow cake was lowered with good economic benefits. (author)

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

CERN Document Server

American Society for Testing and Materials. Philadelphia

2010-01-01

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

Surface preparation process of a uranium titanium alloy, in particular for chemical nickel plating

International Nuclear Information System (INIS)

Henri, A.; Lefevre, D.; Massicot, P.

1987-01-01

In this process the uranium alloy surface is attacked with a solution of lithium chloride and hydrochloric acid. Dissolved uranium can be recovered from the solution by an ion exchange resin. Treated alloy can be nickel plated by a chemical process [fr

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

International Nuclear Information System (INIS)

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

2012-01-01

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

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

International Nuclear Information System (INIS)

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

2011-01-01

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

Annotated bibliography of uranium in Australia, 1970-1987

International Nuclear Information System (INIS)

O'Faircheallaigh, C.; Webb, A.; Wade-Marshall, D.

1989-01-01

The bibliography contains 845 separate numbered items which deal with uranium mining in Australia during the period 1970-1987, which it was feasible to annotate, which are publicly available, and which are not of a highly technical nature. The bibliography is not restricted to material originating in Australia. The items are organised into nine major subject areas on the basis of their principal subject matter, with cross references being added in cases where more than one subject area is dealt with. The nine sections deal with the development and structure of the Australian uranium industry; the uranium debate; uranium policies; uranium and Aborigines; economic issues; domestic processing and utilisation of Australian uranium; environmental issues; nuclear proliferation and safeguards; and the major individual uranium projects. The bibliography is preceded by a chapter on its scope, organisation and sources and by an overview providing background information on the nuclear fuel cycle, uranium in Australia and Australian uranium policy and is followed by an author index

Biogeochemical Processes Regulating the Mobility of Uranium in Sediments

Energy Technology Data Exchange (ETDEWEB)

Belli, Keaton M.; Taillefert, Martial

2016-07-01

This book chapters reviews the latest knowledge on the biogeochemical processes regulating the mobility of uranium in sediments. It contains both data from the literature and new data from the authors.

Development of an improved two-cycle process for recovering uranium from wet-process phosphoric acid

International Nuclear Information System (INIS)

Chen, H.M.; Chen, H.J.; Tsai, Y.M.; Lee, T.W.; Ting, G.

1987-01-01

An improved two-cycle separation process for the recovery of uranium from wet-process phosphoric acid by extraction with bis(2-ethylhexyl)phosphoric acid (D2EHPA) plus dibutyl butylphosphonate (DBBP) in kerosene has been developed and demonstrated successfully in bench-scale, continuous mixer-settler tests. The sulfuric acid and water scrubbing steps for the recycled extraction in the second cycle solve the problems of the contamination and dilution of the phosphoric acid by the ammonium ion and water and also avoid the formation of undesirable phosphatic precipitates during the subsequent extraction of uranium by recycled organic extractant

Chemical process for recovery of uranium values contained in phosphoric mineral lixivia

International Nuclear Information System (INIS)

Conceicao, E.L.H. da; Awwal, M.A.; Coelho, S. V.

1980-01-01

A recovery process of uranium values from phosporic mineral lixivia for obtaining uranio oxide concentrate adjusted to specifications of purity for its commercialization the process consists of the adjustment of electromotive force of lixiviem to suitable values for uranium extraction, extraction with organic solvent containing phosphoric acid ester and oxidant reextraction from this solvent with phosphoric acid solution, suggesting a new solvent extraction containing synergetic mixture of di-2-ethyl hexyl phosphoric acid and tri-octyl phosphine, leaching this solvent with water and re-extraction/precipitation with ammonium carbonate solution, resulting in the formation of uranyl tricarbonate and ammonium, that by drying and calcination gives the uranium oxide with purity degree for commercialization. (M.C.K.) [pt

PHWR fuel fabrication with imported uranium - procedures and processes

International Nuclear Information System (INIS)

Rao, R.V.R.L.V.; Rameswara Rao, A.; Hemantha Rao, G.V.S.; Jayaraj, R.N.

2010-01-01

Following the 123 agreement and subsequent agreements with IAEA & NSG, Government of India has entered into bilateral agreements with different countries for nuclear trade. Department of Atomic Energy (DAE), Government of India, has entered into contract with few countries for supply of uranium material for use in the safeguarded PHWRs. Nuclear Fuel Complex (NFC), an industrial unit of DAE, established in the early seventies, is engaged in the production of Nuclear Fuel and Zircaloy items required for Nuclear Power Reactors operating in the country. NFC has placed one of its fuel fabrication facilities (NFC, Block-A, INE-) under safeguards. DAE has opted to procure uranium material in the form of ore concentrate and fuel pellets. Uranium ore concentrate was procured as per the ASTM specifications. Since no international standards are available for PHWR fuel pellets, Specifications have to be finalized based on the present fabrication and operating experience. The process steps have to be modified and fine tuned for handling the imported uranium material especially for ore concentrate. Different transportation methods are to be employed for transportation of uranium material to the facility. Cost of the uranium material imported and the recoveries at various stages of fuel fabrication have impact on the fuel pricing and in turn the unit energy costs. Similarly the operating procedures have to be modified for safeguards inspections by IAEA. NFC has successfully manufactured and supplied fuel bundles for the three 220 MWe safeguarded PHWRs. The paper describes various issues encountered while manufacturing fuel bundles with different types of nuclear material. (author)

Uranium recovery from wet-process phosphoric acid with octylphenyl acid phosphate. Progress report

International Nuclear Information System (INIS)

Arnold, W.D.; McKamey, D.R.; Baes, C.F.

1980-01-01

Studies were continued of a process for recovering uranium from wet-process phosphoric acid with octylphenyl acid phosphate (OPAP), a mixture of mono- and dioctylphenyl phosphoric acids. The mixture contained at least nine impurities, the principal one being octyl phenol, and also material that readily hydrolyzed to octyl phenol and orthophosphoric acid. The combination of mono- and dioctylphenyl phosphoric acids was the principal uranium extractant, but some of the impurities also extracted uranium. Hydrolysis of the extractant had little effect on uranium extraction, as did the presence of moderate concentrations of octyl phenol and trioctylphenyl phosphate. Diluent choice among refined kerosenes, naphthenic mixtures, and paraffinic hydrocarbons also had little effect on uranium extraction, but extraction was much lower when an aromatic diluent was used. Purified OPAP fractions were sparingly soluble in aliphatic hydrocarbon diluents. The solubility was increased by the presence of impurities such as octyl phenol, and by the addition of water or an acidic solution to the extractant-diluent mixture. In continuous stability tests, extractant loss by distribution to the aqueous phase was much less to wet-process phosphoric acid than to reagent grade acid. Uranium recovery from wet-process acid decreased steadily because of the combined effects of extractant poisoning and precipitation of the extractant as a complex with ferric iron. Unaccountable losses of organic phase volume occurred in the continuous tests. While attempts to recover the lost organic phase were unsuccessful, the test results indicate it was not lost by entrainment or dissolution in the phosphoric acid solutions. 21 figures, 8 tables

Processing of irradiated, enriched uranium fuels at the Savannah River Plant

Energy Technology Data Exchange (ETDEWEB)

Hyder, M L; Perkins, W C; Thompson, M C; Burney, G A; Russell, E R; Holcomb, H P; Landon, L F

1979-04-01

Uranium fuels containing /sup 235/U at enrichments from 1.1% to 94% are processed and recovered, along with neptunium and plutonium byproducts. The fuels to be processed are dissolved in nitric acid. Aluminum-clad fuels are disssolved using a mercury catalyst to give a solution rich in aluminum. Fuels clad in more resistant materials are dissolved in an electrolytic dissolver. The resulting solutions are subjected to head-end treatment, including clarification and adjustment of acid and uranium concentration before being fed to solvent extraction. Uranium, neptunium, and plutonium are separated from fission products and from one another by multistage countercurrent solvent extraction with dilute tri-n-butyl phosphate in kerosene. Nitric acid is used as the salting agent in addition to aluminum or other metal nitrates present in the feed solution. Nuclear safety is maintained through conservative process design and the use of monitoring devices as secondary controls. The enriched uranium is recovered as a dilute solution and shipped off-site for further processing. Neptunium is concentrated and sent to HB-Line for recovery from solution. The relatively small quantities of plutonium present are normally discarded in aqueous waste, unless the content of /sup 238/Pu is high enough to make its recovery desirable. Most of the /sup 238/Pu can be recovered by batch extraction of the waste solution, purified by counter-current solvent extraction, and converted to oxide in HB-Line. By modifying the flowsheet, /sup 239/Pu can be recovered from low-enriched uranium in the extraction cycle; neptunium is then not recovered. The solvent is subjected to an alkaline wash before reuse to remove degraded solvent and fission products. The aqueous waste is concentrated and partially deacidified by evaporation before being neutralized and sent to the waste tanks; nitric acid from the overheads is recovered for reuse.

Processing of irradiated, enriched uranium fuels at the Savannah River Plant

International Nuclear Information System (INIS)

Hyder, M.L.; Perkins, W.C.; Thompson, M.C.; Burney, G.A.; Russell, E.R.; Holcomb, H.P.; Landon, L.F.

1979-04-01

Uranium fuels containing 235 U at enrichments from 1.1% to 94% are processed and recovered, along with neptunium and plutonium byproducts. The fuels to be processed are dissolved in nitric acid. Aluminum-clad fuels are disssolved using a mercury catalyst to give a solution rich in aluminum. Fuels clad in more resistant materials are dissolved in an electrolytic dissolver. The resulting solutions are subjected to head-end treatment, including clarification and adjustment of acid and uranium concentration before being fed to solvent extraction. Uranium, neptunium, and plutonium are separated from fission products and from one another by multistage countercurrent solvent extraction with dilute tri-n-butyl phosphate in kerosene. Nitric acid is used as the salting agent in addition to aluminum or other metal nitrates present in the feed solution. Nuclear safety is maintained through conservative process design and the use of monitoring devices as secondary controls. The enriched uranium is recovered as a dilute solution and shipped off-site for further processing. Neptunium is concentrated and sent to HB-Line for recovery from solution. The relatively small quantities of plutonium present are normally discarded in aqueous waste, unless the content of 238 Pu is high enough to make its recovery desirable. Most of the 238 Pu can be recovered by batch extraction of the waste solution, purified by counter-current solvent extraction, and converted to oxide in HB-Line. By modifying the flowsheet, 239 Pu can be recovered from low-enriched uranium in the extraction cycle; neptunium is then not recovered. The solvent is subjected to an alkaline wash before reuse to remove degraded solvent and fission products. The aqueous waste is concentrated and partially deacidified by evaporation before being neutralized and sent to the waste tanks; nitric acid from the overheads is recovered for reuse

Lung cancer among workers at a uranium processing plant

International Nuclear Information System (INIS)

Cookfair, D.L.; Beck, W.L.; Shy, C.; Lushbaugh, C.C.; Sowder, C.L.

1983-01-01

This study examined the risk of dying from lung cancer among white males who received radiation to the lung as a result of inhaling uranium dust or the dust of uranium compounds. Cases and controls were chosen from a cohort of workers employed in a uranium processing plant during World War II. Cumulative radiation lung dose among study population members ranged from 0 to 75 rads. Relative risk was found to increase with increasing level of exposure even after controlling for age and smoking status, but only for those who were over the age of 45 when first exposed. A statistically significant excess in risk was found for men in this age group with a cumulative lung dose of 20 rads of more. These data suggest that older age groups may be more susceptible to radiation-induced lung cancer than younger age groups

Data feature World natural Uranium production 1992

International Nuclear Information System (INIS)

Anon.

1993-01-01

NUKEM estimates that world uranium production fell more than 13% last year, from 40,729 tonnes U [106 million lbs U308] in 1991 to 35,363 tonnes U [92 million lbs U308] in 1992. Production fell in both the Western World and non-Western World. How much of demand was met by production? World uranium production in 1992 amounted to about 65% of reactor consumption. That's assuming that reactor demand of the non-Western World has not changed much from the Uranium Institute's estimate for 1991. Civilian stockpiles are being drawn down on a massive scale while the world waits to see what will become of the military stockpiles that could soon enter the global supply picture

The relationship of JNC and JCO in the uranium processing plant criticality accident

International Nuclear Information System (INIS)

Kanamori, Masashi; Yanagibashi, Katsumi; Okamoto, Naritoshi

2002-12-01

On September 30th 1999, the criticality accident occurred at JCO's uranium conversion building in Tokai. The accident occurred during reconversion from U 3 O 8 to uranium nitrate solution (UNH) with uranium enriched 18.8% and about 60 kgU. JCO contacted with JNC to supply UNH that is fuel material for the experimental fast breeder reactor 'JOYO'. JNC has contracted with JCO that had started nuclear fuel material processing business following a definite policy of Japanese government and developed SUMITOMO ADU PROCESS'. JNC made the first contract with JCO in 1985 and has made a contact every year. There had never been a problem in their products. JNC inspected products based on contract. JNC discharge our duty as customer inspecting products based on contract. As for safety control, JCO had taken licensing safety review and had been permitted to be 'a processing facility'. Therefore JNC understood that JCO produced following this license. 'The Uranium Processing Plant Criticality Accident Investigation' showed that JCO had been taking a different method from the permit and violating the license. However JNC had never been explained about that and JCO's operation procedures had never described about that. Therefore the Criticality Accident couldn't be avoided. This report describes the relationship of JNC and JCO in the uranium reconversion contract for JOYO, atomic development policy of Japanese government, process to the order and the contents of contract. (author)

Recovery of uranium by a reverse osmosis process

International Nuclear Information System (INIS)

Cleary, J.G.; Stana, R.R.

1980-01-01

A method for concentrating and recovering uranium material from an aqueous solution, comprises passing a feed solution containing uranium through at least one reverse osmosis membrane system to concentrate the uranium, and then flushing the concentrated uranium solution with water in a reverse osmosis membrane system to further concentrate the uranium

Uranium geochemistry in a calcareous peat: mineral-organic-microorganisms interactions and implications on uranium mobility in a contaminated soil

International Nuclear Information System (INIS)

Phrommavanh, V.; Descostes, M.; L'Orphelin, J.M.; Beaucaire, C.; Gaudet, J.P.

2009-01-01

The authors discuss the different approaches and techniques which have been implemented to study the behaviour of uranium in an as complex medium as a natural peat, in this case, a calcareous peat located on an old industrial site which was dedicated to uranium processing and which is now being decontaminated. They report and comment a chemical and mineralogical characterization of this peat, its hydrochemical characterization, and a microbial flora characterization

Influence of uranium and thorium in the natural radioactivity in shales from the middle Amazon river region

International Nuclear Information System (INIS)

Ferro, A.L.

1982-02-01

The feasibility of using the fission track registration technique in the determination of the uranium and thorium content in shales from the middle Amazon river region is studied. The above technique permits, through the determination of the uranium concentration, to establish a correlation between the uranium content and the organic matter present in the shale. In establishing the ratio between the fission tracks due to 238 U and 235 U, the sample was contaminated with natural uranium and analized, so that no modifications on the analysis conditions might change or distort the results. The experimental results were satisfactory and they may contribute to the study of the industrial exploration of these energy sources as well as to the analysis of problems related to environmental control. (Author) [pt

The use of uranium fluxes as safety indicators of radioactive waste repositories

International Nuclear Information System (INIS)

Miller, W.M.; Hooker, P.J.

2002-01-01

Natural analogues based on uranium deposits are commonly used to represent the long-term behaviour of radioactive waste repositories or the processes that influence their radioactive contents. The geochemical dispersion of naturally occurring uranium can also be used to model natural radioactivity fluxes in the vicinity of a planned repository. These fluxes can be estimated for erosional and groundwater discharge processes and compared with calculated future fluxes of radioactivity that would be released from a repository. The methodology is outlined and the benefits of the approach for supporting the derivation of a safety case for a repository are indicated. (author)

Extraction of uranium from sea water with the granular composite adsorbent by using the fixed bed

International Nuclear Information System (INIS)

Katoh, Shunsaku; Sakane, Kohji; Hirotsu, Takahiro; Fujii, Ayako; Kitamura, Takao

1981-01-01

To clarify the technical problems existing in the extraction process of uranium from sea water, uranium was extracted from natural sea water, with the granulated C-Ti-OH composite adsorbent. The adsorption of uranium from sea water was carried out by using the fixed bed that had been designed in our laboratory. The uranium recovery from the sea water was 13.9% in the adsorption process of 56 d. The adsorbed uranium was eluted from the adsorbent with 0.5 N NaHCO 3 -0.5N Na 2 CO 3 soln. at 70 0 C. The elution recovery was 97.4% for 35 h. The uranium contained in the eluate was concentrated twenty times as much as in the anion exchange process, and then 100 times in the solvent extraction process with oxine-chloroform and TOA-kerosene. About 0.7 g of yellow cake was prepared from natural sea water, and it was identified to be pure 2UO 2 .NH 3 .3H 2 O by X-ray diffraction method and X-ray fluorometry. (author)