Method for converting uranium oxides to uranium metal

International Nuclear Information System (INIS)

Duerksen, W.K.

1988-01-01

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

Debye temperatures of uranium chalcogenides from their lattice ...

Indian Academy of Sciences (India)

Unknown

From the phonon frequencies, their Debye temperatures are evaluated. Further, ... Keywords. Uranium chalcogenides; p-wave electronic superconductor; phonon frequency; Debye tempera- ture; spin ... to the ionic crystals of similar structure.

U3O8 obtained from metallic uranium

International Nuclear Information System (INIS)

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

2003-01-01

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

AC measurements on uranium doped high temperature superconductors

International Nuclear Information System (INIS)

Eisterer, M.

1999-11-01

The subject of this thesis is the influence of fission tracks on the superconducting properties of melt textured Y-123. The critical current densities, the irreversibility lines and the transition temperature were determined by means of ac measurements. The corresponding ac techniques are explored in detail. Deviations of the ac signal from the expectations according to the Bean model were explained by the dependence of the shielding currents on the electric field. This explanation is supported by the influence of the ac amplitude and frequency on the critical current density but also by a comparison of the obtained data with other experimental techniques. Y-123 has to be doped with uranium in order to induce fission tracks. Uranium forms normal conducting clusters, which are nearly spherical, with a diameter of about 300 nm. Fission of uranium-235 by thermal neutrons creates two high energy ions with a total energy of about 160 MeV. Each of these fission products induces a linear defect with a diameter of about 10 nm. The length of one fission track is 2-4 μm. At 77 K the critical current density is enhanced by the pinning action of the uranium clusters, compared to undoped samples. With decreasing temperature this influence becomes negligible. The critical current densities are strongly enhanced due to the irradiation. At low magnetic fields we find extremely high values for melt textured materials, e.g. 2.5x10 9 Am -2 at 77 K and 0.25 T or 6x10 10 Am -2 at 5 K. Since the critical current was found to be inverse proportional to the square root of the applied magnetic field it decreases rapidly as the field increases. This behavior is predicted by simple theoretical considerations, but is only valid at low temperatures as well as in low magnetic fields at high temperatures. At high fields the critical current drops more rapidly. The irreversibility lines are only slightly changed by this irradiation technique. Only a small shift to higher fields and temperatures

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.

Stability with temperature of mixed uranium plutonium monocarbides

International Nuclear Information System (INIS)

Riglet-Martial, Ch.; Dumas, J.C.; Piron, J.P.; Gueneau, Ch.

2008-01-01

Full text: Among the different advanced fuel materials of concern for Generation IV systems, the mixed carbide of uranium and plutonium fuel is considered as one of the key materials for Gas Fast Reactors (GFR) systems. For purposes of optimising its fabrication process as well as its performances in various operating conditions, the losses of gaseous plutonium specially at elevated temperatures have to be controlled and minimized. The paper is therefore concerned with a parametric analysis of the stability with temperature of mixed carbides of uranium and plutonium. Previous published experimental studies have shown that mixed (U ,Pu) carbides undergo a highly incongruent sublimation at high temperatures: the vapour phase in equilibrium with the solid is mainly composed of gaseous plutonium (P Pu /P total > 99 % ) while the contribution of gaseous U and C remains very low. The composition of the system U 1-z Pu z C 1+x ' (z =Pu/(U+Pu) and x C/(U+Pu)), the temperature (T) and the expansion volume (V) of the gas are the main parameters in the loss of gaseous Pu. The calculations are carried out using the SAGE (Solgasmix Advanced Gibbs Energy) software, by assuming ideal solid solutions between UC and PuC, as well as between U 2 C 3 and Pu 2 C 3 . The validity of the model is previously tested using published equilibrium vapour pressure data. This work gives rise to a large description of the variations of Pu losses from mixed uranium plutonium carbides and leads to some basic recommendations in connection with the use of this advanced fuel materials

Study about uranium oxides at high temperature by X-ray diffraction

International Nuclear Information System (INIS)

Costa, M.I.

1978-01-01

In this work a technique to study the lattice parameters in the crystalline substances at hight temperature by X-rays diffraction is developed. The results obtained agree very well with the experimental data found in the literature. The crystalline structure of uranium oxide at different temperature is studied in detail by this technique. At the range of the temperature investigated, i.e., 20 0 C to 640 0 C, the following forms for uranium oxide: U 3 O 8 in its hexagonal modification, cubic UO 2 , cubic U 4 O 9 and tetragonal U 3 O 7 is observed. The appearance of two hexagonal units observed in this work is identified by Milne. A good reproducibillity is observed for measurements at the same temperature [pt

Detection of uranium extraction zone by axial temperature profiles in a pulsed column for Purex process

International Nuclear Information System (INIS)

Tsukada, T.; Takahashi, K.

1991-01-01

A new method was presented for detecting uranium extraction zone in a pulsed column by means of measuring axial temperature profile originated from reaction heat during uranium extraction. Key parameters of the temperature profiles were estimated with a code developed for calculating temperature profiles in a direct-contact heat exchanger such as a pulsed column, and were verified using data from a small pulsed column simulating reaction heat with injecting hot water. Finally, the results were compared with those from an actual uranium extraction tests, indicating that the method presented was promising for detecting uranium extraction zone in a pulsed column. (author)

Airborne uranium, its concentration and toxicity in uranium enrichment facilities

International Nuclear Information System (INIS)

Thomas, J.; Mauro, J.; Ryniker, J.; Fellman, R.

1979-02-01

The release of uranium hexafluoride and its hydrolysis products into the work environment of a plant for enriching uranium by means of gas centrifuges is discussed. The maximum permissible mass and curie concentration of airborne uranium (U) is identified as a function of the enrichment level (i.e., U-235/total U), and chemical and physical form. A discussion of the chemical and radiological toxicity of uranium as a function of enrichment and chemical form is included. The toxicity of products of UF 6 hydrolysis in the atmosphere, namely, UO 2 F 2 and HF, the particle size of toxic particulate material produced from this hydrolysis, and the toxic effects of HF and other potential fluoride compounds are also discussed. Results of an investigation of known effects of humidity and temperature on particle size of UO 2 F 2 produced by the reaction of UF 6 with water vapor in the air are reported. The relationship of the solubility of uranium compounds to their toxic effects was studied. Identification and discussion of the standards potentially applicable to airborne uranium compounds in the working environment are presented. The effectiveness of High Efficiency Particulate (HEPA) filters subjected to the corrosive environment imposed by the presence of hydrogen fluoride is discussed

An unusual temperature dependence in the oxidation of oxycarbide layers on uranium

Science.gov (United States)

Ellis, Walton P.

1981-09-01

An anomalous temperature dependence has been observed for the oxidation kinetics of outermost oxycarbide layers on polycrystalline uranium metal. Normally, oxidation or corrosion reactions are expected to proceed more rapidly as the temperature is elevated. Thus, it came as a surprise when we observed that the removal of the outermost atomic layers of carbon from uranium oxycarbide by O 2 reproducibly proceeds at a much faster rate at 25°C than at 280°C.

Release of gases from uranium metal at high temperatures

International Nuclear Information System (INIS)

Sayi, Y.S.; Ramanjaneyulu, P.S.; Yadav, C.S.; Shankaran, P.S.; Chhapru, G.C.; Ramakumar, K.L.; Venugopal, V.

2008-01-01

Depending on the ambient environmental conditions, different gaseous species could get entrapped in uranium metal ingots or pellets. On heating, melting or vapourising uranium metal, these get released and depending on the composition, may cause detrimental effects either within the metal matrix itself or on the surrounding materials/environment. For instance, these gases may affect the performance of the uranium metal, which is used as fuel in the heavy water moderated research reactors, CIRUS and DHRUVA. Hence, detailed investigations have been carried out on the release of gases over a temperature range 875-1500 K employing hot vacuum extraction technique, in specimen uranium pellets made from uranium rods/ingots. Employing an on-line quadrupole mass spectrometer, the analysis of released gases was carried out. The isobaric interference between carbon monoxide and nitrogen at m/e = 28 in the mass spectrometric analysis has been resolved by considering their fragmentation patterns. Since no standards are available to evaluate the results, only the reproducibility is tested. The precision (relative standard deviation at 3σ level) of the method is ±5%. The minimum detectable gas content employing the method is 5.00 x 10 -09 m 3 . About 4 x 10 -04 m 3 /kg of gas is released from uranium pellets, with hydrogen as the main constituent. The gas content increases with storage in air

Spectroscopic measurements of plasma temperatures and electron number density in a uranium hollow cathode discharge lamp

International Nuclear Information System (INIS)

Shah, M.L.; Suri, B.M.; Gupta, G.P.

2015-01-01

The HCD (Hollow Cathode Discharge) lamps have been used as a source of free atoms of any metal, controllable by direct current in the lamp. The plasma parameters including neutral species temperature, atomic excitation temperature and electron number density in a see-through type, homemade uranium hollow cathode discharge lamp with neon as a buffer gas have been investigated using optical emission spectroscopic techniques. The neutral species temperature has been measured using the Doppler broadening of a neon atomic spectral line. The atomic excitation temperature has been measured using the Boltzmann plot method utilizing uranium atomic spectral lines. The electron number density has been determined from the Saha-Boltzmann equation utilizing uranium atomic and ionic spectral lines. To the best of our knowledge, all these three plasma parameters are simultaneously measured for the first time in a uranium hollow cathode discharge lamp

Mid-depth temperature maximum in an estuarine lake

Science.gov (United States)

Stepanenko, V. M.; Repina, I. A.; Artamonov, A. Yu; Gorin, S. L.; Lykossov, V. N.; Kulyamin, D. V.

2018-03-01

The mid-depth temperature maximum (TeM) was measured in an estuarine Bol’shoi Vilyui Lake (Kamchatka peninsula, Russia) in summer 2015. We applied 1D k-ɛ model LAKE to the case, and found it successfully simulating the phenomenon. We argue that the main prerequisite for mid-depth TeM development is a salinity increase below the freshwater mixed layer, sharp enough in order to increase the temperature with depth not to cause convective mixing and double diffusion there. Given that this condition is satisfied, the TeM magnitude is controlled by physical factors which we identified as: radiation absorption below the mixed layer, mixed-layer temperature dynamics, vertical heat conduction and water-sediments heat exchange. In addition to these, we formulate the mechanism of temperature maximum ‘pumping’, resulting from the phase shift between diurnal cycles of mixed-layer depth and temperature maximum magnitude. Based on the LAKE model results we quantify the contribution of the above listed mechanisms and find their individual significance highly sensitive to water turbidity. Relying on physical mechanisms identified we define environmental conditions favouring the summertime TeM development in salinity-stratified lakes as: small-mixed layer depth (roughly, ~wind and cloudless weather. We exemplify the effect of mixed-layer depth on TeM by a set of selected lakes.

Uranium casting furnace automatic temperature control development

International Nuclear Information System (INIS)

Lind, R.F.

1992-01-01

Development of an automatic molten uranium temperature control system for use on batch-type induction casting furnaces is described. Implementation of a two-color optical pyrometer, development of an optical scanner for the pyrometer, determination of furnace thermal dynamics, and design of control systems are addressed. The optical scanning system is shown to greatly improve pyrometer measurement repeatability, particularly where heavy floating slag accumulations cause surface temperature gradients. Thermal dynamics of the furnaces were determined by applying least-squares system identification techniques to actual production data. A unity feedback control system utilizing a proportional-integral-derivative compensator is designed by using frequency-domain techniques. 14 refs

Emission characteristics of uranium hexafluoride at high temperatures

International Nuclear Information System (INIS)

Krascella, N.L.

1976-01-01

An experimental study was conducted to ascertain the spectral characteristics of uranium hexafluoride (UF 6 ) and possible UF 6 thermal decomposition products as a function of temperature and pressure. Relative emission measurements were made for UF 6 /Argon mixtures heated in a plasma torch over a range of temperatures from 800 to about 3600 0 K over a wavelength range from 80 to 600 nm. Total pressures were varied from 1 to approximately 1.7 atm. Similarly absorption measurements were carried out in the visible region from 420 to 580 nm over a temperature range from about 1000 to 1800 0 K. Total pressure for these measurements was 1.0 atm

Maximum Temperature Detection System for Integrated Circuits

Science.gov (United States)

Frankiewicz, Maciej; Kos, Andrzej

2015-03-01

The paper describes structure and measurement results of the system detecting present maximum temperature on the surface of an integrated circuit. The system consists of the set of proportional to absolute temperature sensors, temperature processing path and a digital part designed in VHDL. Analogue parts of the circuit where designed with full-custom technique. The system is a part of temperature-controlled oscillator circuit - a power management system based on dynamic frequency scaling method. The oscillator cooperates with microprocessor dedicated for thermal experiments. The whole system is implemented in UMC CMOS 0.18 μm (1.8 V) technology.

Coarsening-densification transition temperature in sintering of uranium dioxide

International Nuclear Information System (INIS)

Balakrishna, Palanki; Narasimha Murty, B.; Chakraborthy, K.P.; Jayaraj, R.N.; Ganguly, C.

2001-01-01

The concept of coarsening-densification transition temperature (CDTT) has been proposed to explain the experimental observations of the study of sintering undoped uranium dioxide and niobia-doped uranium dioxide powder compacts in argon atmosphere in a laboratory tubular furnace. The general method for deducing CDTT for a given material under the prevailing conditions of sintering and the likely variables that influence the CDTT are described. Though the present work is specific in nature for uranium dioxide sintering in argon atmosphere, the concept of CDTT is fairly general and must be applicable to sintering of any material and has immense potential to offer advantages in designing and/or optimizing the profile of a sintering furnace, in the diagnosis of the fault in the process conditions of sintering, and so on. The problems of viewing the effect of heating rate only in terms of densification are brought out in the light of observing the undesirable phenomena of coring and bloating and causes were identified and remedial measures suggested

On the separation of so-called non-volatile uranium fission products of uranium using the conversion of neutron-irradiated uranium dioxide and graphite

International Nuclear Information System (INIS)

Elhardt, W.

1979-01-01

The investigations are continued in the following work which arose from the concept of separating uranium fission products from uranium. This is achieved in that due to the lattice conversions occurring during the course of solid chemical reactions, fission products can easily pass from the uranium-contained solid to a second solid. The investigations carried out primarily concern the release behaviour of cerium and neodymium in the temperature region of 1200 to 1700 0 C. UO 2 + graphite, both in powder form, are selected as suitable reaction system having the preconditions needed for the lattice conversion for the release effect. The target aimed at from the practical aspect for the improved release of lanthanoids is achieved by an isobar test course - changing temperature from 1200 to 1500 0 C at constant pressure, with a cerium release of 75-80% and a neodynium release of 80-90% (maximum at 1400 0 C). The concepts on the mechanism of the fission product release are related to transport processes in crystal lattices, as well as chemical solid reactions and evaporation processes on the surface of UC 2 grains. (orig./RB) [de

Uranium-thorium fuel cycle in a very high temperature hybrid system

International Nuclear Information System (INIS)

Hernandez, C.R.G.; Oliva, A.M.; Fajardo, L.G.; Garcia, J.A.R.; Curbelo, J.P.; Abadanes, A.

2011-01-01

Thorium is a potentially valuable energy source since it is about three to four times as abundant as Uranium. It is also a widely distributed natural resource readily accessible in many countries. Therefore, Thorium fuels can complement Uranium fuels and ensure long term sustainability of nuclear power. The main advantages of the use of a hybrid system formed by a Pebble Bed critical nuclear reactor and two Pebble Bed Accelerator Driven Systems (ADSs) using a Uranium-Thorium (U + Th) fuel cycle are shown in this paper. Once-through and two step U + Th fuel cycle was evaluated. With this goal, a preliminary conceptual design of a hybrid system formed by a Graphite Moderated Gas-Cooled Very High Temperature Reactor and two ADSs is proposed. The main parameters related to the neutronic behavior of the system in a deep burn scheme are optimized. The parameters that describe the nuclear fuel breeding and Minor Actinide stockpile are compared with those of a simple Uranium fuel cycle. (author)

Uranium energy dependence

International Nuclear Information System (INIS)

Erkes, P.

1981-06-01

Uranium supply and demand as projected by the Uranium Institute is discussed. It is concluded that for the industrialized countries, maximum energy independence is a necessity. Hence it is necessary to achieve assurance of supply for uranium used in thermal power reactors in current programs and eventually to move towards breeders

RECOVERY OF URANIUM FROM ZIRCONIUM-URANIUM NUCLEAR FUELS

Science.gov (United States)

Gens, T.A.

1962-07-10

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

Study of the low temperature oxidation of uranium powders and its application to the sintering of uranium oxide powders; Etude de l'oxydation des poudres dtranium a basse temperature et son application au frittage de poudres d'uranium oxyde

Energy Technology Data Exchange (ETDEWEB)

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

1964-06-01

The uranium oxygen reaction has been studied with a view to obtaining U-UO{sub 2} samples containing about 20 per cent by weight of UO{sub 2} starting from spherical grain uranium powder (36 {mu} < {phi} < 50 {mu}). The techniques used are micrography, thermogravimetry, sintering under pressure, radio-crystallography. At 170 deg. C in air or argon + oxygen mixtures, the uranium oxide formed is always UO{sub 2} and it is uniformly distributed around the initial uranium spheres. These mixed powders can easily be sintered under pressure in the {gamma}-phase. The density of the samples obtained is 85 to 90 per cent of the theoretical density. The influence of UO{sub 2} on the properties of uranium has been shown by the use of dilatometry and thermal cycling in the {alpha} phase. The temperatures at which the phase changes {alpha} {r_reversible} {beta} and {beta} {r_reversible} {gamma} occur are lowered, the remnant expansion is decreased. High density samples resist well to thermal cycling; the characteristic defects of uranium: high distortion, wrinkled surface, have almost disappeared. Heat treatments in a secondary vacuum at 1050 deg. C cause crystallization of UO{sub 2} in a geometrical form and the appearance of a phase of the F.C.C. crystalline type having the composition U{sub W}C{sub X}O{sub Y}N{sub Z}. This phase causes a new decrease in the {alpha} {r_reversible} {beta}, {beta} {r_reversible} {gamma} transformation temperatures for the uranium. After ten dilatometric cycles the remanent expansion of the sample is about 0.5 per cent. The resistance to thermal cycling of a low density sample which has been heat-treated is similar to that of a high density sample which has not undergone a heat treatment. (author) [French] La reaction uranium-oxygene a ete etudiee pour permettre l'obtention d'echantillons U-UO{sub 2} a 20 pour cent en poids environ d'UO{sub 2}, a partir de billes d'uranium pulverulent (36 {mu} < {phi} < 50 {mu}). Les

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)

Influence of the temperature in the uranium (Vi) sorption in zirconium diphosphate

International Nuclear Information System (INIS)

Garcia G, N.; Solis, D.; Ordonez R, E.

2012-10-01

In the present work was evaluated the uranium (Vi) sorption at 10, 20, 30, 40 and 60 C on the zirconium diphosphate (ZrP 2 O 7 ). They were carried out kinetic and isotherms using the method by lots, these will allow to fix the sorption time (kinetic) and to explain the behavior of this sorption in different ph conditions and temperature (isotherm). The quantity of retained uranium in the surface was quantified by means of the fluorescence technique. (Author)

Anomalous thermal property behaviour of uranium at low temperatures

International Nuclear Information System (INIS)

Sandenaw, T.A.

1975-01-01

Low temperature heat capacity curves are presented for polycrystalline 235 U and 238 U metals in different microstructural states and of different purities. Thermal conductivity versus temperature curves are shown for low-purity, polycrystalline 238 U in the temperature range between approximately 80 and 373 0 K for metal having undergone varied fabrication procedures. Published information suggests that there will be no structural modification in very pure uranium below room temperature. The influence of impurities on low temperature transitions may be through their effects on dislocation formation. Thermal conductivity and heat capacity runs started at approximately 80 0 K, after holding specimens at the temperature of boiling liquid nitrogen, do not give results which match up with runs started below 36 to 43 0 K. Result of measurements started at approximately 80 0 K indicate that an ordering mechanism is predominating, with microstructure rather than purity being the important factor. This can be explained if ordering at approximately 80 0 K is through lattice imperfections remaining from prior specimen processing. The drop off in heat capacity appearing above 36 0 K in the C/sub p/ versus T curves of 235 U and 238 U suggest the possibility of: (1) heat evolution from a developing antiphase structure or (2) heat evolution similar to that noted with a quenched martensite. Physical property changes in 238 U at 250 to 270 0 K and at 325 to 350 0 K seem to be related to the heat evolution which starts at 36 0 K during adiabatic heat capacity measurements. The data from heat capacity and thermal conductivity measurements are analyzed to help explain the significance of the sometimes very slight physical property changes observed at 36 to 43, approximately 80, 250 to 270 and 325 to 350 0 K in uranium metal. (U.S.)

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.

Mechanical behaviour of uranium; Comportement mecanique de l'uranium

Energy Technology Data Exchange (ETDEWEB)

Bernard, J L; Coureau, G [Commissariat a l' Energie Atomique, Dir. Industrielle, Saclay (France). Centre d' Etudes Nucleaires

1957-07-01

The chief mechanical properties of uranium, taken at room and at different temperatures, are presented in this report. (author) [French] Dans ce rapport sont presentees les principales caracteristiques mecaniques de l'uranium, relevees a l'ambiante et a differentes temperatures. (auteur)

Performance analysis and comparison of an Atkinson cycle coupled to variable temperature heat reservoirs under maximum power and maximum power density conditions

International Nuclear Information System (INIS)

Wang, P.-Y.; Hou, S.-S.

2005-01-01

In this paper, performance analysis and comparison based on the maximum power and maximum power density conditions have been conducted for an Atkinson cycle coupled to variable temperature heat reservoirs. The Atkinson cycle is internally reversible but externally irreversible, since there is external irreversibility of heat transfer during the processes of constant volume heat addition and constant pressure heat rejection. This study is based purely on classical thermodynamic analysis methodology. It should be especially emphasized that all the results and conclusions are based on classical thermodynamics. The power density, defined as the ratio of power output to maximum specific volume in the cycle, is taken as the optimization objective because it considers the effects of engine size as related to investment cost. The results show that an engine design based on maximum power density with constant effectiveness of the hot and cold side heat exchangers or constant inlet temperature ratio of the heat reservoirs will have smaller size but higher efficiency, compression ratio, expansion ratio and maximum temperature than one based on maximum power. From the view points of engine size and thermal efficiency, an engine design based on maximum power density is better than one based on maximum power conditions. However, due to the higher compression ratio and maximum temperature in the cycle, an engine design based on maximum power density conditions requires tougher materials for engine construction than one based on maximum power conditions

Investigation of uranium (VI) adsorption by polypyrrole

Energy Technology Data Exchange (ETDEWEB)

Abdi, S. [Faculty of Chemical, Petroleum and Gas Engineering, Semnan University, Semnan 35195-363 (Iran, Islamic Republic of); Nasiri, M., E-mail: mnasiri@semnan.ac.ir [Faculty of Chemical, Petroleum and Gas Engineering, Semnan University, Semnan 35195-363 (Iran, Islamic Republic of); Mesbahi, A. [Faculty of Chemical, Petroleum and Gas Engineering, Semnan University, Semnan 35195-363 (Iran, Islamic Republic of); Khani, M.H. [Nuclear Fuel Cycle Research School, Nuclear Science and Technology Research Institute, Tehran, 14395-836 (Iran, Islamic Republic of)

2017-06-15

Highlights: • The adsorbent (polypyrrole) was synthesized by a chemical method using PEG, DBSNa and CTAB as the surfactant. • The solution pH was one of the most important parameters affecting the adsorption of uranium. • The CTAB provided higher removal percentage compared with the other surfactants. • The maximum adsorption capacity obtained from Langmuir isotherm was 87.72 mg/g. • The pseudo second-order model fitted well with the adsorption kinetic of polypyrrole to uranium. - Abstract: The purpose of this study was to investigate the adsorption of uranium (VI) ions on the polypyrrole adsorbent. Polypyrrole was synthesized by a chemical method using polyethylene glycol, sodium dodecylbenzenesulfonate, and cetyltrimethylammonium bromide as the surfactant and iron (III) chloride as an oxidant in the aqueous solution. The effect of various surfactants on the synthesized polymers and their performance as the uranium adsorbent were investigated. Adsorbent properties were characterized by scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) techniques. The effect of different parameters such as pH, contact time, initial metal ion concentrations, adsorbent dose, and the temperature was investigated in the batch system for uranium adsorption process. It has been illustrated that the adsorption equilibrium time is 7 min. The results showed that the Freundlich model had the best agreement and the maximum adsorption capacity of polypyrrole for uranium (VI) was determined 87.72 mg/g from Langmuir isotherm. In addition, the mentioned adsorption process was fast and the kinetic data were fitted to the Pseudo first and second order models. The adsorption kinetic data followed the pseudo-second-order kinetic model. Moreover, the thermodynamic parameters ΔG{sup 0}, ΔH{sup 0} and ΔS{sup 0} showed that the uranium adsorption process by polypyrrole was endothermic and spontaneous.

Uranium recovery by leaching with sodium carbonate at high temperature and pressure

International Nuclear Information System (INIS)

Soerensen, E.; Koefoed, S.; Lundgaard, T.

1983-11-01

The principal uranium bearing mineral in Greenland steenstrupine is a complex sodium REE phosphosilicate in which Fe, Mn, Th, U are minor constituents. The Na 2 CO 3 extractant is used for specially acidconsuming ores. However, steenstrupine is decomposed by Na 2 CO 3 only at temperatures above 220degC, so the leaching must be carried out under pressure. Laboratory tests have shown the optimal temperature to be 260degC and the leach liquor composition120 g/l of NaHCO 3 and 20 g/l of Na 2 CO 3 . Addition of oxygen is necessary as uranium will not dissolve in carbonate unless it is brought in its highest state of oxidation. According to the laboratory tests it may be estimated that 1 kg of ore suspended in 1 l of leach liquor and ground to 80% minus 200 mesh can be extracted in 20-40 minutes. On the basis of data obtained a process was suggested in which the ore is ground with carbonate leach liquor to a suitable suspension which is fed to an autoclave with a retentiontime of 20 minutes at 260degC. The residue is filtered off and the liquor reused for grinding and ex- traction. The demand for a reaction temperature near 300degC, a pressure up to 120 atm. and a continuos operation favours a tubular flow autoclave with so narrow a bore that the turbulence provides the mechanical agitation of the suspension. From the mined material it appears that more than 80% of the uranium can be extracted in the pipe autoclave. Some samples give off the obtainable uranium in 20 minutes. The precipitated yellow cake is contaminated with more Na and Si than admitted by international standards. (EG)

Study of algae's adsorption to uranium ion in water solution

International Nuclear Information System (INIS)

Du Yang; Qiu Yongmei; Dan Guiping; Zhang Dong; Lei Jiarong

2007-01-01

The adsorption efficiencies of the algae to uranium ion were determined at various pH, uranium ion concentrations, adsorption temperatures and the species of coexisted metal ions, and the effect of coexisted metal ion on the adsorption efficiency was researched. The experimental results at pH= 5-8 are as follows. 1) the adsorption capacity is a constant to be about 1.40 μg/g for the Yantai red alga and the sea spinach, and is changeable in the range of 1.03-2.23 μg/g with pH for the sea edible fungus; 2) for the algae the adsorption efficiency and adsorption capacity are related to uranium ion concentration, and the maximum adsorption efficiency and capacity is 95.8% and 65.4 μg/g, respectively; 3) the adsorption process for 24 h is not dependent on the temperature; 4) the effect of the species of coexisted metal ions on the adsorption capacity of uranium ion is various with the time during adsorption process. (authors)

Temperature effect on uranium retention onto Zr2O(PO4)2 surface

International Nuclear Information System (INIS)

Almazan Torres, M.G.

2007-03-01

Uranium sorption onto Zr 2 O(PO 4 ) 2 has been studied between 298 K and 363 K, in 0.1 M NaClO 4 medium. Potentiometric titrations were realized to determine temperature dependency of the acid-base properties (pH(pcn), acidity constants). Classical batch experiments were performed at different temperatures. The sorption experiments revealed that the uranium sorption onto Zr 2 O(PO 4 ) 2 is favoured with the temperature. Structural characterization of the surface complexes was performed by both Time-Resolved Laser-Induced Fluorescence (TRLIF) and EXAFS spectroscopy. The TRLIF measurements vs. temperature revealed two uranyl surface complexes. No influence of the temperature onto the nature surface complex was observed. The EXAFS analysis showed a splitting of the equatorial oxygen atoms in two shells, corresponding to uranyl bidentate, inner-sphere complexes. The obtained structural uranyl surface complex information was used to simulate (using a constant capacitance model) the sorption edges. The proposed complexes equilibrium model consists of the following surface complexes: (ZrOH) 2 UO 2 2+ and (PO) 2 UO 2 . Besides the stability constants for the surface complexes, the thermodynamic parameters ΔH 0 and ΔS 0 were determined using the van't Hoff equation. The enthalpy values associated to the U(VI) retention onto Zr 2 O(PO 4 ) 2 , determined by the temperature dependence of the stability constants, testify that the formation of the complex (PO) 2 UO 2 (55 kJ/mol) is endothermic, while no influence of the temperature was observed for the formation of the complex (ZrOH) 2 UO 2 2+ . The adsorption reaction of the last complex is then driven by entropy. In addition, calorimetric measurements of uranium sorption onto Zr 2 O(PO 4 ) 2 were carried out to directly quantify the enthalpy associated to the retention processes. (author)

Magnetic graphene based nanocomposite for uranium scavenging

Energy Technology Data Exchange (ETDEWEB)

El-Maghrabi, Heba H. [Egyptian Petroleum Research Institute, 11727, Cairo (Egypt); Abdelmaged, Shaimaa M. [Nuclear Materials Authority, 6530 P.O. Box Maadi, Cairo (Egypt); Nada, Amr A. [Egyptian Petroleum Research Institute, 11727, Cairo (Egypt); Zahran, Fouad, E-mail: f.zahran@quim.ucm.es [Faculty of Science, Helwan University, 11795, Cairo (Egypt); El-Wahab, Saad Abd; Yahea, Dena [Faculty of Science, Ain shams University, Cairo (Egypt); Hussein, G.M.; Atrees, M.S. [Nuclear Materials Authority, 6530 P.O. Box Maadi, Cairo (Egypt)

2017-01-15

Graphical abstract: Graphical representation of U{sup 6+} adsorption on Magnetic Ferberite-Graphene Nanocomposite. - Highlights: • Synthesis of new magnetic wolframite bimetallic nanostructure on graphene. • A promising adsorption capacity of 455 mg/g was recorded for FG-20 within 60 min at room temperature. • The uranium removal was followed pseudo-second order kinetics and Langmuir isotherm. - Abstract: Magnetic graphene based ferberite nanocomposite was tailored by simple, green, low cost and industrial effective method. The microstructure and morphology of the designed nanomaterials were examined via XRD, Raman, FTIR, TEM, EDX and VSM. The prepared nanocomposites were introduced as a novel adsorbent for uranium ions scavenging from aqueous solution. Different operating conditions of time, pH, initial uranium concentration, adsorbent amount and temperature were investigated. The experimental data shows a promising adsorption capacity. In particular, a maximum value of 455 mg/g was obtained within 60 min at room temperature with adsorption efficiency of 90.5%. The kinetics and isotherms adsorption data were fitted with the pseudo-second order model and Langmuir equation, respectively. Finally, the designed nanocomposites were found to have a great degree of sustainability (above 5 times of profiteering) with a complete maintenance of their parental morphology and adsorption capacity.

Study of the transformation of uranium-niobium alloys with low niobium concentrations, tempered from the gamma and beta + gamma 1 regions and then annealed at different temperatures. Comparison with uranium-molybdenum alloys (1963); Etude des transformations des alliages uranium-niobium a faible teneur en niobium trempes depuis les domaines gamma et beta + gamma 1 puis revenus a differentes temperatures. Comparaison avec les alliages uranium-molybdene (1963)

Energy Technology Data Exchange (ETDEWEB)

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

1962-09-15

The author shows that uranium-niobium alloys, like uranium-molybdenum alloys, tempered from the gamma region, give a martensitic phase with a structure deriving from that of alpha uranium by a slight contraction parallel to the axis [001], The critical cooling rate allowing the formation of this martensite is 80 deg. C/s at 750 deg. C. Retention of the beta phase of uranium-niobium alloys is particularly difficult, the critical retention rate being 700 deg. C/s at 668 deg. C for an alloy containing 2.5 at. per cent of Nb. This beta phase is completely converted to the alpha phase at room temperature in about 6 hours. The TTT curves of this beta alloy are effectively reduced to the lower branch of the lower 'C'. The beta phase conversion law is expressed as: 1-x = exp. (kt){sup n} x being the degree of progression of the conversion, t the time, n an exponent no-varying with temperature and having approximately the value 2 for the alloy considered, k an increasing function of temperature. The activation energy of conversion is of the order of 14,600 cal/mole. Niobium is much less active than molybdenum as a stabiliser of beta uranium. (author) [French] Dans ce travail l'auteur montre que les alliages uranium-niobium, comme d'ailleurs les alliages uranium-molybdene, trempes depuis le domaine gamma, donnent une phase martensitique dont la structure derive de celle de l'uranium alpha par une legere contraction parallele de l'axe [001]. La vitesse critique de refroidissement permettant la formation de cette martensite est de 80 deg. C/s a 750 deg. C. La retention de la phase beta des alliages uranium-niobium est particulierement delicate car la vitesse critique de retention est de 700 deg. C/s a 668 deg. C pour l'alliage a 2,5 at. pour cent de Nb. Cette phase beta se transforme completement en phase alpha a la temperature ordinaire en 6 heures environ. Les courbes TTT de cet alliage de structure beta se reduisent pratiquement a la branche inferieure du 'C' inferieur. La

Operational forecasting of daily temperatures in the Valencia Region. Part I: maximum temperatures in summer.

Science.gov (United States)

Gómez, I.; Estrela, M.

2009-09-01

Extreme temperature events have a great impact on human society. Knowledge of summer maximum temperatures is very useful for both the general public and organisations whose workers have to operate in the open, e.g. railways, roadways, tourism, etc. Moreover, summer maximum daily temperatures are considered a parameter of interest and concern since persistent heat-waves can affect areas as diverse as public health, energy consumption, etc. Thus, an accurate forecasting of these temperatures could help to predict heat-wave conditions and permit the implementation of strategies aimed at minimizing the negative effects that high temperatures have on human health. The aim of this work is to evaluate the skill of the RAMS model in determining daily maximum temperatures during summer over the Valencia Region. For this, we have used the real-time configuration of this model currently running at the CEAM Foundation. To carry out the model verification process, we have analysed not only the global behaviour of the model for the whole Valencia Region, but also its behaviour for the individual stations distributed within this area. The study has been performed for the summer forecast period of 1 June - 30 September, 2007. The results obtained are encouraging and indicate a good agreement between the observed and simulated maximum temperatures. Moreover, the model captures quite well the temperatures in the extreme heat episodes. Acknowledgement. This work was supported by "GRACCIE" (CSD2007-00067, Programa Consolider-Ingenio 2010), by the Spanish Ministerio de Educación y Ciencia, contract number CGL2005-03386/CLI, and by the Regional Government of Valencia Conselleria de Sanitat, contract "Simulación de las olas de calor e invasiones de frío y su regionalización en la Comunidad Valenciana" ("Heat wave and cold invasion simulation and their regionalization at Valencia Region"). The CEAM Foundation is supported by the Generalitat Valenciana and BANCAIXA (Valencia, Spain).

Reaction of water vapor with a clean liquid uranium surface

International Nuclear Information System (INIS)

Siekhaus, W.

1985-01-01

To study the reaction of water vapor with uranium, we have exposed clean liquid uranium surfaces to H 2 O under UHV conditions. We have measured the surface concentration of oxygen as a function of exposure, and determined the maximum attainable surface oxygen concentration X 0 /sup s/ as a function of temperature. We have used these measurements to estimate, close to the melting point, the solubility of oxygen (X 0 /sup b/, -4 ) and its surface segregation coefficient β/sup s/(> 10 3 ). 8 refs., 5 figs., 1 tab

Melting temperature of uranium - plutonium mixed oxide fuel

Energy Technology Data Exchange (ETDEWEB)

Ishii, Tetsuya; Hirosawa, Takashi [Power Reactor and Nuclear Fuel Development Corp., Oarai, Ibaraki (Japan). Oarai Engineering Center

1997-08-01

Fuel melting temperature is one of the major thermodynamical properties that is used for determining the design criteria on fuel temperature during irradiation in FBR. In general, it is necessary to evaluate the correlation of fuel melting temperature to confirm that the fuel temperature must be kept below the fuel melting temperature during irradiation at any conditions. The correlations of the melting temperature of uranium-plutonium mixed oxide (MOX) fuel, typical FBR fuel, used to be estimated and formulized based on the measured values reported in 1960`s and has been applied to the design. At present, some experiments have been accumulated with improved experimental techniques. And it reveals that the recent measured melting temperatures does not agree well to the data reported in 1960`s and that some of the 1960`s data should be modified by taking into account of the recent measurements. In this study, the experience of melting temperature up to now are summarized and evaluated in order to make the fuel pin design more reliable. The effect of plutonium content, oxygen to metal ratio and burnup on MOX fuel melting was examined based on the recent data under the UO{sub 2} - PuO{sub 2} - PuO{sub 1.61} ideal solution model, and then formulized. (J.P.N.)

Melting temperature of uranium - plutonium mixed oxide fuel

International Nuclear Information System (INIS)

Ishii, Tetsuya; Hirosawa, Takashi

1997-08-01

Fuel melting temperature is one of the major thermodynamical properties that is used for determining the design criteria on fuel temperature during irradiation in FBR. In general, it is necessary to evaluate the correlation of fuel melting temperature to confirm that the fuel temperature must be kept below the fuel melting temperature during irradiation at any conditions. The correlations of the melting temperature of uranium-plutonium mixed oxide (MOX) fuel, typical FBR fuel, used to be estimated and formulized based on the measured values reported in 1960's and has been applied to the design. At present, some experiments have been accumulated with improved experimental techniques. And it reveals that the recent measured melting temperatures does not agree well to the data reported in 1960's and that some of the 1960's data should be modified by taking into account of the recent measurements. In this study, the experience of melting temperature up to now are summarized and evaluated in order to make the fuel pin design more reliable. The effect of plutonium content, oxygen to metal ratio and burnup on MOX fuel melting was examined based on the recent data under the UO 2 - PuO 2 - PuO 1.61 ideal solution model, and then formulized. (J.P.N.)

Performance and metallography of a uranium tritide bed operated at elevated temperatures and tritium pressures

International Nuclear Information System (INIS)

Mote, M.W. Jr.; Mintz, J.M.

1986-12-01

A uranium gettering bed was cycled between room temperature/zero pressure and 600C/275 psi (D 2 ) for 210 cycles over a period of 8 months. Metallographic examination of the hardware revealed an acceptable amount of reaction between the uranium and the stainless steel container. This exposure is estimated to represent about ten years of normal use

Modeling maximum daily temperature using a varying coefficient regression model

Science.gov (United States)

Han Li; Xinwei Deng; Dong-Yum Kim; Eric P. Smith

2014-01-01

Relationships between stream water and air temperatures are often modeled using linear or nonlinear regression methods. Despite a strong relationship between water and air temperatures and a variety of models that are effective for data summarized on a weekly basis, such models did not yield consistently good predictions for summaries such as daily maximum temperature...

Influence of aliphatic amides on the temperature of maximum density of water

International Nuclear Information System (INIS)

Torres, Andrés Felipe; Romero, Carmen M.

2017-01-01

Highlights: • The addition of amides decreases the temperature of maximum density of water suggesting a disruptive effect on water structure. • The amides in aqueous solution do not follow the Despretz equation in the concentration range considered. • The temperature shift Δθ as a function of molality is represented by a second order equation. • The Despretz constants were determined considering the dilute concentration region for each amide solution. • Solute disrupting effect of amides becomes smaller as its hydrophobic character increases. - Abstract: The influence of dissolved substances on the temperature of the maximum density of water has been studied in relation to their effect on water structure as they can change the equilibrium between structured and unstructured species of water. However, most work has been performed using salts and the studies with small organic solutes such as amides are scarce. In this work, the effect of acetamide, propionamide and butyramide on the temperature of maximum density of water was determined from density measurements using a magnetic float densimeter. Densities of aqueous solutions were measured within the temperature range from T = (275.65–278.65) K at intervals of 0.50 K in the concentration range between (0.10000 and 0.80000) mol·kg −1 . The temperature of maximum density was determined from the experimental results. The effect of the three amides is to decrease the temperature of maximum density of water and the change does not follow the Despretz equation. The results are discussed in terms of solute-water interactions and the disrupting effect of amides on water structure.

Study of uranium-titanium diffusion; Etude de la diffusion uranium-titane

Energy Technology Data Exchange (ETDEWEB)

Adda, Y; Philibert, J [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires; Institut de Recherches de la Siderurgie Francaise (IRSID), 78 - Saint-Germain-en-Laye (France)

1959-07-01

In the overall scheme of research on the chemical diffusion of uranium and the transition metals we have studied the uranium-titanium system. The diffusion couples are prepared by welding together small plates of uranium and titanium under pressure, using a technique already described by us. After diffusion under vacuum, polished sections of the samples were micro-graphically examined. This inspection showed that intergranular diffusion occurred at temperatures below 650 deg. C. At higher temperatures, the diffusion occurred uniquely throughout the volume of the metal, and the diffusion zone appeared as a succession of micro-graphically distinguishable bands. Study of the rate of increase of these corresponding 'penetration coefficients'. In addition, we have observed important variations in microhardness within the diffusion zone, we have tried to relate these variations to the variation of concentration. This is measured with the Castaing microprobe. We have thus accurately established the concentration-penetration curves for temperatures between 950 and 1075 deg. C. From these curves, we have calculated the diffusion coefficient D as a function of the concentration using Matano's method. At all temperatures, D(c) curve has a U form as for the U-Zr system. The activation energy has a maximum value of 42 kcal/g atom at an atomic concentration of 0,5. Even though we have rarely seen pores in the diffusion zone, we have nevertheless observed an important Kirkendall-effect by studying the displacements x{sub i} of the interface using tungsten wires as markers. These displacements can be expressed as a function of time and temperature by the equation: x{sub i} = 0,9 t {sup 1/2} exp ( - 14600/(RT)). Finally, using Darken's equations we calculated the intrinsic diffusion coefficients Du and Dti as well as the corresponding activation energies. These energies are similar (QU = 38,5 and QTi = 40 kcal/at. g) and also almost the same as those found for the U-Zr system

Effects of fasting on maximum thermogenesis in temperature-acclimated rats

Science.gov (United States)

Wang, L. C. H.

1981-09-01

To further investigate the limiting effect of substrates on maximum thermogenesis in acute cold exposure, the present study examined the prevalence of this effect at different thermogenic capabilities consequent to cold- or warm-acclimation. Male Sprague-Dawley rats (n=11) were acclimated to 6, 16 and 26‡C, in succession, their thermogenic capabilities after each acclimation temperature were measured under helium-oxygen (21% oxygen, balance helium) at -10‡C after overnight fasting or feeding. Regardless of feeding conditions, both maximum and total heat production were significantly greater in 6>16>26‡C-acclimated conditions. In the fed state, the total heat production was significantly greater than that in the fasted state at all acclimating temperatures but the maximum thermogenesis was significant greater only in the 6 and 16‡C-acclimated states. The results indicate that the limiting effect of substrates on maximum and total thermogenesis is independent of the magnitude of thermogenic capability, suggesting a substrate-dependent component in restricting the effective expression of existing aerobic metabolic capability even under severe stress.

First-principles study on oxidation effects in uranium oxides and high-pressure high-temperature behavior of point defects in uranium dioxide

Science.gov (United States)

Geng, Hua Y.; Song, Hong X.; Jin, K.; Xiang, S. K.; Wu, Q.

2011-11-01

Formation Gibbs free energy of point defects and oxygen clusters in uranium dioxide at high-pressure high-temperature conditions are calculated from first principles, using the LSDA+U approach for the electronic structure and the Debye model for the lattice vibrations. The phonon contribution on Frenkel pairs is found to be notable, whereas it is negligible for the Schottky defect. Hydrostatic compression changes the formation energies drastically, making defect concentrations depend more sensitively on pressure. Calculations show that, if no oxygen clusters are considered, uranium vacancy becomes predominant in overstoichiometric UO2 with the aid of the contribution from lattice vibrations, while compression favors oxygen defects and suppresses uranium vacancy greatly. At ambient pressure, however, the experimental observation of predominant oxygen defects in this regime can be reproduced only in a form of cuboctahedral clusters, underlining the importance of defect clustering in UO2+x. Making use of the point defect model, an equation of state for nonstoichiometric oxides is established, which is then applied to describe the shock Hugoniot of UO2+x. Furthermore, the oxidization and compression behavior of uranium monoxide, triuranium octoxide, uranium trioxide, and a series of defective UO2 at 0 K are investigated. The evolution of mechanical properties and electronic structures with an increase of the oxidation degree are analyzed, revealing the transition of the ground state of uranium oxides from metallic to Mott insulator and then to charge-transfer insulator due to the interplay of strongly correlated effects of 5f orbitals and the shift of electrons from uranium to oxygen atoms.

Design and installation of high-temperature ultrasonic measuring system and grinder for nuclear fuel containing trans-uranium elements

International Nuclear Information System (INIS)

Serizawa, Hiroyuki; Kikuchi, Hironobu; Iwai, Takashi; Arai, Yasuo; Kurosawa, Makoto; Mimura, Hideaki; Abe, Jiro

2005-07-01

A high-temperature ultrasonic measuring system had been designed and installed in a glovebox (711-DGB) to study a mechanical property of nuclear fuel containing trans-uranium (TRU) elements. A figuration apparatus for the cylinder-type sample preparation had also been modified and installed in an established glovebox (142-D). The system consists of an ultrasonic probe, a heating furnace, cooling water-circulating system, a cooling air compressor, vacuum system, gas supplying system and control system. An A/D converter board and an pulsar/receiver board for the measurement of wave velocity were installed in a personal computer. The apparatus was modified to install into the glovebox. Some safety functions were supplied to the control system. The shape and size of the sample was revised to minimize the amount of TRU elements for the use of the measurement. The maximum sample temperature is 1500degC. The performance of the installed apparatuses and the glovebox were confirmed through a series of tests. (author)

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

International Nuclear Information System (INIS)

Miyake, Chie; Hinatsu, Yukio; Imoto, Shosuke

1983-01-01

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

Effective Uranium (VI) Sorption from Alkaline Solutions Using Bi-Functionalized Silica-Coated Magnetic Nanoparticles

International Nuclear Information System (INIS)

Chen, X.; He, L.; Liu, B.; Tang, Y.

2015-01-01

High temperature gas reactor is one of generation IV reactors that can adapt the future energy market, of which the preparation of fuel elements will produce a large amount of radioactive wastewater with uranium and high-level ammonia. Sorption treatment is one of the most important method to recover uranium from wastewater. However, there are few report on uranium sorbent that can directly be applied in wastewater with ammonia. Therefore, the development of a sorbent that can recover uranium in basic environment will greatly decrease the cost of fuel element production and the risk of radioactive pollution. In this work, ammonium-phosphonate-bifunctionalized silica-coated magnetic nanoparticles has been developed for effective sorption of uranium from alkaline media, which are not only advantaged in the uranium separation from liquid phase, but also with satisfactory adsorption rate, amount and reusability. The as-prepared sorbent is found to show a maximum uranium sorption capacity of 70.7 mg/g and a fast equilibrium time of 2 h at pH 9.5 under room temperature. Compared with the mono-functionalized (phosphonate alone and ammonium alone) particles, the combination of the bi-functionalized groups gives rise to an excellent ability to remove uranium from basic environment. The sorbent can be used as a promising solid phase candidate for highly-efficient removal of uranium from basic solution. (author)

A comparison between thorium-uranium and low enrichment uranium cycles in the high temperature reactors

Energy Technology Data Exchange (ETDEWEB)

Cerles, J M

1973-03-15

In a previous report, it was shown that the Uranium cycle could be used as well with multi-hole block (GGA type) as with tubular elements. Now, in a F.S.V. geometry, a comparison is made between Thorium cycle and Uranium cycle. This comparison will be concerned with the physical properties of the materials, the needs of natural Uranium, the fissile material inventory and, at last, an attempt of economical considerations. In this report the cycle will be characterizd by the fertile material. So, we write ''Thorium cycle'' for Highly Enriched Uranium - Thorium cycle and ''Uranium cycle'' for low Enrichment Uranium cycle.

REMOVAL AND CONCENTRATION OF URANIUM FROM WASTE MINE

Directory of Open Access Journals (Sweden)

Elizângela Augusta Santos

2011-01-01

Full Text Available The use of leaching agents, such as sodium citrate and ammonium carbonate, were assessed for the extraction of uranium from one mining residue containing 0.25% U. Concentration techniques such as precipitation and ion exchange were employed to recover the uranium from the leaching liquor. Leaching results showed maximum uranium extraction of about 40% for both reagents. The use 10 mol L-1 NaOH to precipitate the uranium from the leach liquor leads to a recovery of 62%; what was considered not satisfactory. In view of this, resins were used to concentrate the uranium from the liquor and the metal loading obtained at pH 3.9 was higher for the resin DOWEX RPU, whose maximum loading maximum capacity was 148.3 mg g-1, compared to 126.9 mg g-1 presented by the resin IRA 910 U.

Optimization of operating parameters and rate of uranium bioleaching from a low-grade ore

International Nuclear Information System (INIS)

Rashidi, A.; Roosta-Azad, R.; Safdari, S.J.

2014-01-01

In this study the bioleaching of a low-grade uranium ore containing 480 ppm uranium has been reported. The studies involved extraction of uranium using Acidithiobacillus ferrooxidans derived from the uranium mine samples. The maximum specific growth rate (μ max ) and doubling time (t d ) were obtained 0.08 h -1 and 8.66 h, respectively. Parameters such as Fe 2+ concentration, particle size, temperature and pH were optimized. The effect of pulp density (PD) was also studied. Maximum uranium bio-dissolution of 100 ± 5 % was achieved under the conditions of pH 2.0, 5 % PD and 35 deg C in 48 h with the particles of d 80 = 100 μm. The optimum concentration of supplementary Fe 2+ was dependent to the PD. This value was 0 and 10 g of FeSO 4 ·7H 2 O/l at the PD of 5 and 15 %, respectively. The effects of time, pH and PD on the bioleaching process were studied using central composite design. New rate equation was improved for the uranium leaching rate. The rate of leaching is controlled with the concentrations of ferric and ferrous ions in solution. This study shows that uranium bioleaching may be an important process for the Saghand U mine at Yazd (Iran). (author)

Extraction of uranium from seawater

International Nuclear Information System (INIS)

Kanno, M.

1977-01-01

The nuclear power generation is thought to be very important in Japan. However, known domestic uranium resources in Japan are very rare. So, extraction of uranium from sea water have been carried out since 1962 at Japan Tobacco and Salt Public Corporation. There are a number of results obtained also by Kyoto University, Shikoku Govenment Industrial Research Institute, Tokyo University and others. In order to investigate the technical and economical feasibility of extraction of uranium and other resources from sea water, a research program was started in fiscal 1975, sponsored by the Ministry of International Trade and Industry with the budget of about $440,000. In this program, the conceptional design of two types of model plants, the ''column type'' and the ''tidal type'' was drawn on the design bases set up with available information. It was found that there has been several problems waiting solution, but there were no technically fatal problems. Adsorption tests were carried out with adsorbents of more than eleven types, including titanium hydroxide, and it was found that titanium hydroxide made by titanyl surphate and urea had the largest adsorption capacity of uranium among them. Elution experiments were performed only with ammonium carbonate and the efficiency at the temperature of 60 0 C showed three times higher than that of 20 0 C. A few long term column operation was conducted, mainly with the adsorbent of granulated titanium hydroxide for 15-60 days. The maximum yield of uranium throughout the adsorption and elution operation was over 20% and macimum concentration of uranium in eluate was 7 ppm

Removal of uranium ions from synthetic wastewater using ZnO/Na-clinoptilolite nanocomposites

International Nuclear Information System (INIS)

Aghadavoud, Azadeh; Saraee, Khadijeh Rezaee Ebrahim; Shakur, Hamid Reza; Sayyari, Rasol

2016-01-01

Uranium is one of the heavy metals that is found in industrial wastewater and is very toxic for human and environment. In this work, natural clinoptilolite is used as a low-cost adsorbent for uranium removal from aqueous solutions. The sodium form of clinoptilolite and ZnO/Na-clinoptilolite nanocomposite were prepared. The sample sorption capacities for uranium removal from simulated drinking water in the presence of other anions and cations were investigated. Natural zeolite and its modified forms were characterized by XRD, XRF, FTIR, TEM and BET. Batch experiments were used to determine the best adsorption conditions. The effects of various parameters such as contact time, pH, initial uranium concentration, temperature and mass sorbent on the removal efficiency of uranium ions were studied. The equilibration was attained after 2 and 6 h for the Na-clinoptilolite and ZnO/Na-clinoptilolite nanocomposite, respectively. Both adsorbents showed relatively fast adsorption. Effective removal of uranium was demonstrated at pH values of 4-8 for both forms of zeolite. Temperature had no significant effect on adsorption. The maximum removal efficiency of uranium by the ZnO/Na-clinoptilolite nanocomposite in pH=7.2 and room temperature was 98.55%. Langmuir, Freundlich and Sips models were used for describing the equilibrium isotherms for uranium uptake. The Sips model corresponded well with the experimental data. The thermodynamic parameters, such as ΔG , ΔH and ΔS , have been calculated and interpreted. The pseudo-first order and pseudo-second order models were applied to describe the kinetic data. The pseudo-second order kinetic model had excellent kinetic data fitting (R2=1).

Removal of uranium ions from synthetic wastewater using ZnO/Na-clinoptilolite nanocomposites

Energy Technology Data Exchange (ETDEWEB)

Aghadavoud, Azadeh; Saraee, Khadijeh Rezaee Ebrahim; Shakur, Hamid Reza [Isfahan Univ. (Iran, Islamic Republic of). Dept. of Nuclear Engineering; Sayyari, Rasol

2016-07-01

Uranium is one of the heavy metals that is found in industrial wastewater and is very toxic for human and environment. In this work, natural clinoptilolite is used as a low-cost adsorbent for uranium removal from aqueous solutions. The sodium form of clinoptilolite and ZnO/Na-clinoptilolite nanocomposite were prepared. The sample sorption capacities for uranium removal from simulated drinking water in the presence of other anions and cations were investigated. Natural zeolite and its modified forms were characterized by XRD, XRF, FTIR, TEM and BET. Batch experiments were used to determine the best adsorption conditions. The effects of various parameters such as contact time, pH, initial uranium concentration, temperature and mass sorbent on the removal efficiency of uranium ions were studied. The equilibration was attained after 2 and 6 h for the Na-clinoptilolite and ZnO/Na-clinoptilolite nanocomposite, respectively. Both adsorbents showed relatively fast adsorption. Effective removal of uranium was demonstrated at pH values of 4-8 for both forms of zeolite. Temperature had no significant effect on adsorption. The maximum removal efficiency of uranium by the ZnO/Na-clinoptilolite nanocomposite in pH=7.2 and room temperature was 98.55%. Langmuir, Freundlich and Sips models were used for describing the equilibrium isotherms for uranium uptake. The Sips model corresponded well with the experimental data. The thermodynamic parameters, such as ΔG , ΔH and ΔS , have been calculated and interpreted. The pseudo-first order and pseudo-second order models were applied to describe the kinetic data. The pseudo-second order kinetic model had excellent kinetic data fitting (R2=1).

Metallurgical structures in a high uranium-silicon alloy

International Nuclear Information System (INIS)

Wyatt, B.S.; Berthiaume, L.C.; Conversi, J.L.

1968-10-01

The effects of fabrication and heat treatment variables on the structure of a uranium -- 3.96 wt% silicon alloy have been studied using optical microscopy, quantitative metallography and hardness determinations. It has been shown that an optimum temperature exists below the peritectoid temperature where the maximum amount of transformation to U 3 Si occurs in a given period of time. The time required to fully transform an as-cast alloy at this optimum temperature is affected by the size of the primary U 3 Si 2 dendrites. With a U 3 Si 2 particle size of <12 μm complete transformation can be achieved in four hours. (author)

Enriched-uranium feed costs for the High-Temperature Gas-Cooled reactor: trends and comparison with other reactor concepts

International Nuclear Information System (INIS)

Thomas, W.E.

1976-04-01

This report discusses each of the components that affect the unit cost for enriched uranium; that is, ore costs, U 3 O 8 to UF 6 conversion cost, costs for enriching services, and changes in transaction tails assay. Historical trends and announced changes are included. Unit costs for highly enriched uranium (93.15 percent 235 U) and for low-enrichment uranium (3.0, 3.2, and 3.5 percent 235 U) are displayed as a function of changes in the above components and compared. It is demonstrated that the trends in these cost components will probably result in significantly less cost increase for highly enriched uranium than for low-enrichment uranium--hence favoring the High-Temperature Gas-Cooled Reactor

Stochastic modelling of the monthly average maximum and minimum temperature patterns in India 1981-2015

Science.gov (United States)

Narasimha Murthy, K. V.; Saravana, R.; Vijaya Kumar, K.

2018-04-01

The paper investigates the stochastic modelling and forecasting of monthly average maximum and minimum temperature patterns through suitable seasonal auto regressive integrated moving average (SARIMA) model for the period 1981-2015 in India. The variations and distributions of monthly maximum and minimum temperatures are analyzed through Box plots and cumulative distribution functions. The time series plot indicates that the maximum temperature series contain sharp peaks in almost all the years, while it is not true for the minimum temperature series, so both the series are modelled separately. The possible SARIMA model has been chosen based on observing autocorrelation function (ACF), partial autocorrelation function (PACF), and inverse autocorrelation function (IACF) of the logarithmic transformed temperature series. The SARIMA (1, 0, 0) × (0, 1, 1)12 model is selected for monthly average maximum and minimum temperature series based on minimum Bayesian information criteria. The model parameters are obtained using maximum-likelihood method with the help of standard error of residuals. The adequacy of the selected model is determined using correlation diagnostic checking through ACF, PACF, IACF, and p values of Ljung-Box test statistic of residuals and using normal diagnostic checking through the kernel and normal density curves of histogram and Q-Q plot. Finally, the forecasting of monthly maximum and minimum temperature patterns of India for the next 3 years has been noticed with the help of selected model.

Uranium recovery by leaching with sodium carbonate at high temperature and pressure

International Nuclear Information System (INIS)

Soerensen, E.; Koefoed, S.; Lundgaard, T.

1990-09-01

An alkaline rock from the Ilimaussaq instrusion, SW Greenland, was proposed as a source of uranium. Its principal uranium bearing mineral, Steenstrupine, is a complex sodium REE phosphosilicate in which Fe, Mn, Th and U are minor constituents. A special feature of this ore body is the content of water soluble minerals: NaF (Villiaumite), Na 2 Si 2 O 5 (Natrosilite) and an organic substance which displays the characteristics of humus. Sulfides are sparse, the most important one being ZnS (Sphalerite) of which the content is generally less than 0.5%. In the mineral under consideration (Lujavrite) the Steenstrupine is mainly finelay disseminated throughout the rock, yielding a uranium content of 300-400 ppm and thorium content of 800-1000 ppm. Laboratory tests indicated that high temperature carbonate leaching was necessary to decompose Steenstrupine. The optium temperature was shown to be 260 deg. C and the leach liquor composition 120 g/l of NaHCO 3 and 20 g/l of Na 2 C0 3 . Addition of oxygen is necessary. The process was developed to industrial scale in a continuous pipe autoclave with a retention time of 20 min. After filtering on a belt filter, the liquor was recycled several times to obtain a higher U-concentration. By reductive precipitation with iron powder a raw UO 2 was obtained. It was purified after dissolution in HNO 3 . An overall yield of 80% could be obtained. (author) 32 tabs., 13 ills., 24 refs

Uranium luminescence in La2 Zr2 O7 : effect of concentration and annealing temperature.

Science.gov (United States)

Mohapatra, M; Rajeswari, B; Hon, N S; Kadam, R M

2016-12-01

The speciation of a particular element in any given matrix is a prerequisite to understanding its solubility and leaching properties. In this context, speciation of uranium in lanthanum zirconate pyrochlore (La 2 Zr 2 O 7  = LZO), prepared by a low-temperature combustion route, was carried out using a simple photoluminescence lifetime technique. The LZO matrix is considered to be a potential ceramic host for fixing nuclear and actinide waste products generated during the nuclear fuel cycle. Special emphasis has been given to understanding the dynamics of the uranium species in the host as a function of annealing temperature and concentration. It was found that, in the LZO host, uranium is stabilized as the commonly encountered uranyl species (UO 2 2+ ) up to a heat treatment of 500 °C at the surface. Above 500 °C, the uranyl ion is diffused into the matrix as the more symmetric octahedral uranate species (UO 6 6- ). The uranate ions thus formed replace the six-coordinated 'Zr' atoms at regular lattice positions. Further, it was observed that concentration quenching takes place beyond 5 mol% of uranium doping. The mechanism of the quenching was found to be a multipolar interaction. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

METHOD OF ROLLING URANIUM

Science.gov (United States)

Smith, C.S.

1959-08-01

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

Temperature and direction dependence of internal strain and texture evolution during deformation of uranium

Energy Technology Data Exchange (ETDEWEB)

Brown, D.W., E-mail: dbrown@lanl.gov [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Bourke, M.A.M.; Clausen, B.; Korzekwa, D.R.; Korzekwa, R.C.; McCabe, R.J.; Sisneros, T.A.; Teter, D.F. [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States)

2009-06-25

Depleted uranium is of current programmatic interest at Los Alamos National Lab due to its high density and nuclear applications. At room temperature, depleted uranium displays an orthorhombic crystal structure with highly anisotropic mechanical and thermal properties. For instance, the coefficient of thermal expansion is roughly 20 x 10{sup -6} deg. C{sup -1} in the a and c directions, but near zero or slightly negative in the b direction. The innate anisotropy combined with thermo-mechanical processing during manufacture results in spatially varying residual stresses and crystallographic texture, which can cause distortion, and failure in completed parts, effectively wasting resources. This paper focuses on the development of residual stresses and textures during deformation at room and elevated temperatures with an eye on the future development of computational polycrystalline plasticity models based on the known micro-mechanical deformation mechanisms of the material.

Uranium removal from the water supply

International Nuclear Information System (INIS)

Miranzadeh, Mohammad Bagher.

1996-01-01

Uranium can be naturally occurring radionuclides that contaminate some potable water supplies. Uranium is found both in surface water and ground water supplies. The United States Environmental Protection Agency recently proposed a maximum contaminant of 20 micro gram/liter for uranium because of concerns about its association with kidney disease and cancer. uranium can be removed from the supply by strong base anion-resin. Exhausted resin is regenerated by sodium chloride solution. (Author)

Low temperature sintering of hyperstoichiometric uranium dioxide

International Nuclear Information System (INIS)

Chevrel, H.

1991-12-01

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

Fuel Retention Improvement at High Temperatures in Tungsten-Uranium Dioxide Dispersion Fuel Elements by Plasma-Spray Cladding

Science.gov (United States)

Grisaffe, Salvatore J.; Caves, Robert M.

1964-01-01

An investigation was undertaken to determine the feasibility of depositing integrally bonded plasma-sprayed tungsten coatings onto 80-volume-percent tungsten - 20-volume-percent uranium dioxide composites. These composites were face clad with thin tungsten foil to inhibit uranium dioxide loss at elevated temperatures, but loss at the unclad edges was still significant. By preheating the composite substrates to approximately 3700 degrees F in a nitrogen environment, metallurgically bonded tungsten coatings could be obtained directly by plasma spraying. Furthermore, even though these coatings were thin and somewhat porous, they greatly inhibited the loss of uranium dioxide. For example, a specimen that was face clad but had no edge cladding lost 5.8 percent uranium dioxide after 2 hours at 4750 dgrees F in flowing hydrogen. A similar specimen with plasma-spray-coated edges, however, lost only 0.75 percent uranium dioxide under the same testing conditions.

The temperature coefficient of the resonance integral for uranium metal and oxide

Energy Technology Data Exchange (ETDEWEB)

Blomberg, P; Hellstrand, E; Homer, S

1960-06-15

The temperature coefficient of the resonance integral in uranium metal and oxide has been measured over a wide temperature range for rods with three different diameters. The results for metal agree with most earlier results from activation measurements but differ as much as a factor of two from results obtained with reactivity methods. For oxide only one measurement has been reported recently. Our value is considerably lower than the result of that measurement. The experiments will continue in order to find the reason for the large discrepancy mentioned above.

The temperature coefficient of the resonance integral for uranium metal and oxide

International Nuclear Information System (INIS)

Blomberg, P.; Hellstrand, E.; Homer, S.

1960-06-01

The temperature coefficient of the resonance integral in uranium metal and oxide has been measured over a wide temperature range for rods with three different diameters. The results for metal agree with most earlier results from activation measurements but differ as much as a factor of two from results obtained with reactivity methods. For oxide only one measurement has been reported recently. Our value is considerably lower than the result of that measurement. The experiments will continue in order to find the reason for the large discrepancy mentioned above

Subtropical Arctic Ocean temperatures during the Palaeocene/Eocene thermal maximum

Science.gov (United States)

Sluijs, A.; Schouten, S.; Pagani, M.; Woltering, M.; Brinkhuis, H.; Damste, J.S.S.; Dickens, G.R.; Huber, M.; Reichart, G.-J.; Stein, R.; Matthiessen, J.; Lourens, L.J.; Pedentchouk, N.; Backman, J.; Moran, K.; Clemens, S.; Cronin, T.; Eynaud, F.; Gattacceca, J.; Jakobsson, M.; Jordan, R.; Kaminski, M.; King, J.; Koc, N.; Martinez, N.C.; McInroy, D.; Moore, T.C.; O'Regan, M.; Onodera, J.; Palike, H.; Rea, B.; Rio, D.; Sakamoto, T.; Smith, D.C.; St John, K.E.K.; Suto, I.; Suzuki, N.; Takahashi, K.; Watanabe, M. E.; Yamamoto, M.

2006-01-01

The Palaeocene/Eocene thermal maximum, ???55 million years ago, was a brief period of widespread, extreme climatic warming, that was associated with massive atmospheric greenhouse gas input. Although aspects of the resulting environmental changes are well documented at low latitudes, no data were available to quantify simultaneous changes in the Arctic region. Here we identify the Palaeocene/Eocene thermal maximum in a marine sedimentary sequence obtained during the Arctic Coring Expedition. We show that sea surface temperatures near the North Pole increased from ???18??C to over 23??C during this event. Such warm values imply the absence of ice and thus exclude the influence of ice-albedo feedbacks on this Arctic warming. At the same time, sea level rose while anoxic and euxinic conditions developed in the ocean's bottom waters and photic zone, respectively. Increasing temperature and sea level match expectations based on palaeoclimate model simulations, but the absolute polar temperatures that we derive before, during and after the event are more than 10??C warmer than those model-predicted. This suggests that higher-than-modern greenhouse gas concentrations must have operated in conjunction with other feedback mechanisms-perhaps polar stratospheric clouds or hurricane-induced ocean mixing-to amplify early Palaeogene polar temperatures. ?? 2006 Nature Publishing Group.

Study of reactions between uranium-plutonium mixed oxide and uranium nitride and between uranium oxide and uranium nitride; Etude des reactions entre l`oxyde mixte d`uranium-plutonium et le nitrure d`uranium et entre l`oxyde d`uranium et le nitrure d`uranium

Energy Technology Data Exchange (ETDEWEB)

Lecraz, C

1993-06-11

A new type of combustible elements which is a mixture of uranium nitride and uranium-plutonium oxide could be used for Quick Neutrons Reactors. Three different studies have been made on the one hand on the reactions between uranium nitride (UN) and uranium-plutonium mixed oxide (U,Pu)O{sub 2}, on the other hand on these between UN and uranium oxide UO{sub 2}. They show a sizeable reaction between nitride and oxide for the studied temperatures range (1573 K to 1973 K). This reaction forms a oxynitride compound, MO{sub x} N{sub y} with M=U or M=(U,Pu), whose crystalline structure is similar to oxide`s. Solubility of nitride in both oxides is studied, as the reaction kinetics. (TEC). 32 refs., 48 figs., 22 tabs.

Uninterrupted thermoelectric energy harvesting using temperature-sensor-based maximum power point tracking system

International Nuclear Information System (INIS)

Park, Jae-Do; Lee, Hohyun; Bond, Matthew

2014-01-01

Highlights: • Feedforward MPPT scheme for uninterrupted TEG energy harvesting is suggested. • Temperature sensors are used to avoid current measurement or source disconnection. • MPP voltage reference is generated based on OCV vs. temperature differential model. • Optimal operating condition is maintained using hysteresis controller. • Any type of power converter can be used in the proposed scheme. - Abstract: In this paper, a thermoelectric generator (TEG) energy harvesting system with a temperature-sensor-based maximum power point tracking (MPPT) method is presented. Conventional MPPT algorithms for photovoltaic cells may not be suitable for thermoelectric power generation because a significant amount of time is required for TEG systems to reach a steady state. Moreover, complexity and additional power consumption in conventional circuits and periodic disconnection of power source are not desirable for low-power energy harvesting applications. The proposed system can track the varying maximum power point (MPP) with a simple and inexpensive temperature-sensor-based circuit without instantaneous power measurement or TEG disconnection. This system uses TEG’s open circuit voltage (OCV) characteristic with respect to temperature gradient to generate a proper reference voltage signal, i.e., half of the TEG’s OCV. The power converter controller maintains the TEG output voltage at the reference level so that the maximum power can be extracted for the given temperature condition. This feedforward MPPT scheme is inherently stable and can be implemented without any complex microcontroller circuit. The proposed system has been validated analytically and experimentally, and shows a maximum power tracking error of 1.15%

Chlorination of uranium ore for extraction of uranium, thorium and radium and for pyrite removal

International Nuclear Information System (INIS)

Skeaf, J.M.

1979-01-01

The high-temperature chlorination of uranium ore was investigated. The objective was to develop a process which is both economically viable and environmentally acceptable. Test work was directed toward obtaining high extractions of uranium, thorium and radium-226, as well as iron, sulphur and the rare earths, and consists of chlorinating samples of an Elliot Lake uranium ore at elevated temperatures and repulping the resulting calcine in dilute hydrochloric acid. The effect of temperature and chlorine throughput on the extraction of the various metals was investigated. The best conditions yielded extractions of uranium, iron and sulphur (all as chlorides) greater than 95 percent. Chlorine consumption varied between 6 and 16 percent by weight of the ore charge. (author)

Uranium dioxide pellets

International Nuclear Information System (INIS)

Zawidzki, T.W.

1982-01-01

A process for the preparation of a sintered, high density, large crystal grain size uranium dioxide pellet is described which involves: (i) reacting a uranyl nitrate of formula UO 2 (NO 3 ) 2 .6H 2 O with a sulphur source, at a temperature of from about 300 deg. C to provide a sulphur-containing uranium trioxide; (ii) reacting the thus-obtained modified uranium trioxide with ammonium nitrate to form an insoluble sulphur-containing ammonium uranate; (iii) neutralizing the thus-formed slurry with ammonium hydroxide to precipitate out as an insoluble ammonium uranate the remaining dissolved uranium; (iv) recovering the thus-formed precipitates in a dry state; (v) reducing the dry precipitate to UO 2 , and forming it into 'green' pellets; and (vi) sintering the pellets in a hydrogen atmosphere at an elevated temperature

Purification of uranium metal

International Nuclear Information System (INIS)

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

1993-01-01

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

An unusual feature of uranium ore from Domiasiat, Meghalaya: presence of water soluble uranium

International Nuclear Information System (INIS)

Singh, A.K.; Padmanabhan, N.P.H.; Sivaramakrishnan, K.; Krishna Rao, N.

1993-01-01

An unusual feature of the recently discovered sandstone-type uranium deposit in Domiasiat is the presence of appreciable amount of water soluble uranium. With normal tap water at its natural pH (7.5-7.8), upto 35% of the uranium in the ore was found to be soluble during agitation in the different samples. Presence of other ions in appreciable quantities particularly SO 4 -2 Cl - and Fe +3 appear to influence the dissolution. Percolation experiments give terminal solubilization of upto 58%, but the instantaneous uranium concentration in the percolating water attains its maximum within the first few minutes of contact. A detailed study on the chemistry of uranium dissolution may throw light on the physico-chemical controls of localization of uranium in the deposit. (author). 7 refs., 3 tabs., 4 tabs

Precise coulometric titration of uranium in a high-purity uranium metal and in uranium compounds

International Nuclear Information System (INIS)

Tanaka, Tatsuhiko; Yoshimori, Takayoshi

1975-01-01

Uranium in uranyl nitrate, uranium trioxide and a high-purity uranium metal was assayed by the coulometric titration with biamperometric end-point detection. Uranium (VI) was reduced to uranium (IV) by solid bismuth amalgam in 5M sulfuric acid solution. The reduced uranium was reoxidized to uranium (VI) with a large excess of ferric ion at a room temperature, and the ferrous ion produced was titrated with the electrogenerated manganese(III) fluoride. In the analyses of uranium nitrate and uranium trioxide, the results were precise enough when the error from uncertainty in water content in the samples was considered. The standard sample of pure uranium metal (JAERI-U4) was assayed by the proposed method. The sample was cut into small chips of about 0.2g. Oxides on the metal surface were removed by the procedure shown by National Bureau of Standards just before weighing. The mean assay value of eleven determinations corrected for 3ppm of iron was (99.998+-0.012) % (the 95% confidence interval for the mean), with a standard deviation of 0.018%. The proposed coulometric method is simple and permits accurate and precise determination of uranium which is matrix constituent in a sample. (auth.)

URANIUM BISMUTHIDE DISPERSION IN MOLTEN METAL

Science.gov (United States)

Teitel, R.J.

1959-10-27

The formation of intermetallic bismuth compounds of thorium or uranium dispersed in a liquid media containing bismuth and lead is described. A bismuthide of uranium dispersed in a liquid metal medium is formed by dissolving uranium in composition of lead and bismuth containing less than 80% lead and lowering the temperature of the composition to a temperature below the point at which the solubility of uranium is exceeded and above the melting point of the composition.

Study of electrolytic reduction of uranium VI to uranium IV in nitrate systems

Energy Technology Data Exchange (ETDEWEB)

Araujo, B.F. de; Almeida, S.G. de; Forbicini, S; Matsuda, H T; Araujo, J.A. de [Instituto de Pesquisas Energeticas e Nucleares, Sao Paulo (Brazil). Centro de Engenharia Quimica

1980-01-01

Experimental parameters are optimized in order to obtain uranium (IV) nitrate solutions at maximum yield, using hydrazine as stabilizer. Uranium (VI) electrolytic reduction was chosen because: there is no increase in the volume of radioactive effluents; there are no secondary reactions; there is no need for further separations; all reagents used are not inflammable. The method is, therefore, efficient and of low cost.

High temperature chlorination of uranium and some radionuclides from rich sulphide ores

International Nuclear Information System (INIS)

Mahdy, M.A.

1992-01-01

This work is concerned with the application of the high temperature chlorination technique upon a sulphide-rich uranium ore from elliot lake, ontario, canada. The purpose is to find a substitute to conventional sulphuric acid leaching which involves both acid drainage and radionuclide dissolution problems. Test work has therefore been directed towards studying some relevant factors of chlorination beside the effect of a number of additives

Maximum Smoke Temperature in Non-Smoke Model Evacuation Region for Semi-Transverse Tunnel Fire

OpenAIRE

B. Lou; Y. Qiu; X. Long

2017-01-01

Smoke temperature distribution in non-smoke evacuation under different mechanical smoke exhaust rates of semi-transverse tunnel fire were studied by FDS numerical simulation in this paper. The effect of fire heat release rate (10MW 20MW and 30MW) and exhaust rate (from 0 to 160m3/s) on the maximum smoke temperature in non-smoke evacuation region was discussed. Results show that the maximum smoke temperature in non-smoke evacuation region decreased with smoke exhaust rate. Plug-holing was obse...

Statistical assessment of changes in extreme maximum temperatures over Saudi Arabia, 1985-2014

Science.gov (United States)

Raggad, Bechir

2018-05-01

In this study, two statistical approaches were adopted in the analysis of observed maximum temperature data collected from fifteen stations over Saudi Arabia during the period 1985-2014. In the first step, the behavior of extreme temperatures was analyzed and their changes were quantified with respect to the Expert Team on Climate Change Detection Monitoring indices. The results showed a general warming trend over most stations, in maximum temperature-related indices, during the period of analysis. In the second step, stationary and non-stationary extreme-value analyses were conducted for the temperature data. The results revealed that the non-stationary model with increasing linear trend in its location parameter outperforms the other models for two-thirds of the stations. Additionally, the 10-, 50-, and 100-year return levels were found to change with time considerably and that the maximum temperature could start to reappear in the different T-year return period for most stations. This analysis shows the importance of taking account the change over time in the estimation of return levels and therefore justifies the use of the non-stationary generalized extreme value distribution model to describe most of the data. Furthermore, these last findings are in line with the result of significant warming trends found in climate indices analyses.

Development of casting techniques for uranium and uranium alloys

International Nuclear Information System (INIS)

Singh, S.P.

2003-01-01

The casting process concerning furnace set-up, mould temperatures, pouring temperatures, out gassing, post heating, casting recovery and crucible and mould clean-up is discussed. Some applications of casting theory can be made in practice, but experience in handling the metal is most valuable in the successful solution of a new problem. The casting of uranium alloys using induction stirring of the melt to promote homogeneity in the casting is described. A few remarks are made concerning safety aspects associated with the casting of uranium

Anticorrosion protection of uranium

Energy Technology Data Exchange (ETDEWEB)

Goncharov, Ivan D.; Kazakovskaya, Tatiana; Tukmakov, Victor; Shapovalov, Vyacheslav [Russian Federal Nuclear Center-VNIIEF, 37, Mira Ave., RU-607190 Sarov (Nizhnii Gorod), 010450 (Russian Federation)

2004-07-01

Uranium in atmospheric conditions is non-stable. Sloughing products are being generated on its surface during storage or use. These corrosion products make many difficulties because of necessity to provide personnel safety. Besides, uranium corrosion may cause damage in parts. The first works devoted to uranium corrosion were performed in the framework of the USA Manhattan Project in the early forties of last century. Various methods of uranium protection were investigated, among them the galvanic one was the most studied. Later on the galvanic technology was patented. The works on this problem remains urgent up to the present time. In Russia, many methods of uranium corrosion protection, mainly against atmospheric corrosion, were tried on. In particular, such methods as diffusion zinc and paint coating were investigated. In the first case, a complex intermetallic U-Zn compound was formed but its protection was not reliable enough, this protection system was inconvenient and uncertain and that is why an additional paint coating was necessary. In the case of paint coatings another problem appeared. It was necessary to find such a coating where gas-permeability would prevail over water-permeability. Otherwise significant uranium corrosion occurs. This circumstance together with low mechanical resistance of paint coatings does not allow to use paint coating for long-term protection of uranium. Currently, there are following methods of uranium protection: ion-plasma, galvanic and thermo-vacuum annealing. These are described in this paper. In the end the issue of corrosion protection in reactor core zones is addressed. Here the greatest difficulties are caused when enriched uranium heated up to 500 deg. C needs anticorrosion protection. In this case various metal coatings are not reliable because of brittle inter-metallide formation. The reliable protection may be provided only up to the temperature plus 400 - 500 deg. C with the help of galvanic copper coating since

Anticorrosion protection of uranium

International Nuclear Information System (INIS)

Goncharov, Ivan D.; Kazakovskaya, Tatiana; Tukmakov, Victor; Shapovalov, Vyacheslav

2004-01-01

Uranium in atmospheric conditions is non-stable. Sloughing products are being generated on its surface during storage or use. These corrosion products make many difficulties because of necessity to provide personnel safety. Besides, uranium corrosion may cause damage in parts. The first works devoted to uranium corrosion were performed in the framework of the USA Manhattan Project in the early forties of last century. Various methods of uranium protection were investigated, among them the galvanic one was the most studied. Later on the galvanic technology was patented. The works on this problem remains urgent up to the present time. In Russia, many methods of uranium corrosion protection, mainly against atmospheric corrosion, were tried on. In particular, such methods as diffusion zinc and paint coating were investigated. In the first case, a complex intermetallic U-Zn compound was formed but its protection was not reliable enough, this protection system was inconvenient and uncertain and that is why an additional paint coating was necessary. In the case of paint coatings another problem appeared. It was necessary to find such a coating where gas-permeability would prevail over water-permeability. Otherwise significant uranium corrosion occurs. This circumstance together with low mechanical resistance of paint coatings does not allow to use paint coating for long-term protection of uranium. Currently, there are following methods of uranium protection: ion-plasma, galvanic and thermo-vacuum annealing. These are described in this paper. In the end the issue of corrosion protection in reactor core zones is addressed. Here the greatest difficulties are caused when enriched uranium heated up to 500 deg. C needs anticorrosion protection. In this case various metal coatings are not reliable because of brittle inter-metallide formation. The reliable protection may be provided only up to the temperature plus 400 - 500 deg. C with the help of galvanic copper coating since

Development of on-line uranium enrichment monitor of gaseous UF6 for uranium enrichment plant

International Nuclear Information System (INIS)

Lu Xuesheng; Liu Guorong; Jin Huimin; Zhao Yonggang; Li Jinghuai; Hao Xueyuan; Ying Bin; Yu Zhaofei

2013-01-01

An on-line enrichment monitor was developed to measure the enrichment of UF 6 , flowing through the processing pipes in uranium enrichment plant. A Nal (Tl) detector was used to measure the count rates of the 185.7 keV γ-ray emitted from 235 U, and the total quantity of uranium was determined from thermodynamic characteristics of gaseous uranium hexafluoride. The results show that the maximum relative standard deviation is less than 1% when the measurement time is 120 s or more and the pressure is more than 2 kPa in the measurement chamber. Uranium enrichment of gaseous uranium hexafluoride in the output end of cascade can be monitored continuously by using the device. It should be effective for nuclear materials accountability verifications and materials balance verification at uranium enrichment plant. (authors)

BfR recommends the establishment of a European maximum level for uranium in drinking and mineral water

OpenAIRE

German Federal Institute for Risk Assessment

2007-01-01

Uranium is a widespread, radioactive heavy metal on earth. It is to be found in varying concentrations and states in various rocks and minerals as well as in water, soil and air. Uranium may also reach the environment anthropogenically for instance in mineral phosphate fertilisers. Because of its widespread presence traces of uranium can also be detected in foods like drinking and mineral water. Uranium is not essential for humans. The ongoing intake of higher uranium concentration...

Recovery and treatment of uranium from uranium-containing solution by liquid membrane emulsion technology

International Nuclear Information System (INIS)

Xia Liangshu; Zhou Yantong; Xiao Yiqun; Peng Anguo; Xiao Jingshui; Chen Wei

2014-01-01

The recovery and treatment of uranium from uranium-containing solution using liquid membrane emulsion (LME) technology were studied in this paper, which contained the best volume ratio of membrane materials, stirring speed during emulsion process, the conditions of extracting, such as temperature, pH, initial concentration of uranium. Moreover, the mechanism for extracting uranium was also discussed. The best experimental conditions of emulsifying were acquired. The volume fractions of P 204 and liquid paraffin are 0.1 and 0.05, the volume ratios of Span80 and sulphonated kerosene to P 204 are 0.06 and 0.79 respectively, stirring speed is controlled in 2 000 r/min, and the concentration of inner phase is 4 mol/L. The recovery rate of uranium is up to 99% through the LME extracted uranium for 0.5 h at pH 2.5 and room temperature when the initial concentration is less than 400 mg/L and the volume ratio is 5 between the uranium-containing waste water and LME. The calculation results of Gibbs free energy show that the reaction process is spontaneous. (authors)

Future changes over the Himalayas: Maximum and minimum temperature

Science.gov (United States)

Dimri, A. P.; Kumar, D.; Choudhary, A.; Maharana, P.

2018-03-01

An assessment of the projection of minimum and maximum air temperature over the Indian Himalayan region (IHR) from the COordinated Regional Climate Downscaling EXperiment- South Asia (hereafter, CORDEX-SA) regional climate model (RCM) experiments have been carried out under two different Representative Concentration Pathway (RCP) scenarios. The major aim of this study is to assess the probable future changes in the minimum and maximum climatology and its long-term trend under different RCPs along with the elevation dependent warming over the IHR. A number of statistical analysis such as changes in mean climatology, long-term spatial trend and probability distribution function are carried out to detect the signals of changes in climate. The study also tries to quantify the uncertainties associated with different model experiments and their ensemble in space, time and for different seasons. The model experiments and their ensemble show prominent cold bias over Himalayas for present climate. However, statistically significant higher warming rate (0.23-0.52 °C/decade) for both minimum and maximum air temperature (Tmin and Tmax) is observed for all the seasons under both RCPs. The rate of warming intensifies with the increase in the radiative forcing under a range of greenhouse gas scenarios starting from RCP4.5 to RCP8.5. In addition to this, a wide range of spatial variability and disagreements in the magnitude of trend between different models describes the uncertainty associated with the model projections and scenarios. The projected rate of increase of Tmin may destabilize the snow formation at the higher altitudes in the northern and western parts of Himalayan region, while rising trend of Tmax over southern flank may effectively melt more snow cover. Such combined effect of rising trend of Tmin and Tmax may pose a potential threat to the glacial deposits. The overall trend of Diurnal temperature range (DTR) portrays increasing trend across entire area with

Precipitation behavior of uranium in multicomponent solution by oxalic acid

International Nuclear Information System (INIS)

Shin, Y.J.; Kim, I.S.; Lee, W.K.; Shin, H.S.; Ro, S.G.

1996-01-01

A study on the precipitation of uranium by oxalic acid was carried out in a multicomponent solution. The precipitation method is usually applied to the treatment of radioactive waste and the recovery of uranium from a uranium-scrap contaminated with impurities. In these cases, the problem is how to increase the precipitation yield of target element and to prevent impurities from coprecipitation. The multicomponent solution in the present experiment was prepared by dissolving U, Nd, Cs and Sr in nitric acid. The effects of concentrations of oxalic acid and ascorbic acid on the precipitation yield and purity of uranium were observed. As results of the study, the maximum precipitation yield of uranium is revealed to be about 96.5% and the relative precipitation ratio of Nd, Cs and Sr versus uranium are discussed at the condition of the maximum precipitation yield of uranium, respectively. (author). 11 refs., 5 figs., 1 tab

Thermal-hydraulic calculations for KUHFR with reduced enrichment uranium fuel

International Nuclear Information System (INIS)

Mishima, Kaichiro; Shibata, Toshikazu.

1982-01-01

This report provides the preliminary results of the thermal-hydraulic calculations to study the safety aspects in fueling the KUHFR with reduced enrichment uranium. The calculations were based on what was outlined in the Safety Analysis Report for the KUHFR and the guidebook for research reactor core conversion, IAEA-TECDOC-233, published by the International Atomic Energy Agency. No significant differences in the thermal-hydraulic operating conditions have been found between HEU and MEU fuels. However, in LEU cases, the combination of three factors - larger power peaking with LEU fuel, smaller thermal conductivity of U 3 O 8 -Al fuel with high uranium densities, and thicker fuel meat - resulted in higher maximum fuel and surface temperatures with the LEU oxide fuel. (author)

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

Assessment of extreme value distributions for maximum temperature in the Mediterranean area

Science.gov (United States)

Beck, Alexander; Hertig, Elke; Jacobeit, Jucundus

2015-04-01

Extreme maximum temperatures highly affect the natural as well as the societal environment Heat stress has great effects on flora, fauna and humans and culminates in heat related morbidity and mortality. Agriculture and different industries are severely affected by extreme air temperatures. Even more under climate change conditions, it is necessary to detect potential hazards which arise from changes in the distributional parameters of extreme values, and this is especially relevant for the Mediterranean region which is characterized as a climate change hot spot. Therefore statistical approaches are developed to estimate these parameters with a focus on non-stationarities emerging in the relationship between regional climate variables and their large-scale predictors like sea level pressure, geopotential heights, atmospheric temperatures and relative humidity. Gridded maximum temperature data from the daily E-OBS dataset (Haylock et al., 2008) with a spatial resolution of 0.25° x 0.25° from January 1950 until December 2012 are the predictands for the present analyses. A s-mode principal component analysis (PCA) has been performed in order to reduce data dimension and to retain different regions of similar maximum temperature variability. The grid box with the highest PC-loading represents the corresponding principal component. A central part of the analyses is the model development for temperature extremes under the use of extreme value statistics. A combined model is derived consisting of a Generalized Pareto Distribution (GPD) model and a quantile regression (QR) model which determines the GPD location parameters. The QR model as well as the scale parameters of the GPD model are conditioned by various large-scale predictor variables. In order to account for potential non-stationarities in the predictors-temperature relationships, a special calibration and validation scheme is applied, respectively. Haylock, M. R., N. Hofstra, A. M. G. Klein Tank, E. J. Klok, P

Uranium geochemistry, mineralogy, geology, exploration and resources

International Nuclear Information System (INIS)

De Vivo, B.

1984-01-01

This book comprises papers on the following topics: history of radioactivity; uranium in mantle processes; transport and deposition of uranium in hydrothermal systems at temperatures up to 300 0 C: Geological implications; geochemical behaviour of uranium in the supergene environment; uranium exploration techniques; uranium mineralogy; time, crustal evolution and generation of uranium deposits; uranium exploration; geochemistry of uranium in the hydrographic network; uranium deposits of the world, excluding Europe; uranium deposits in Europe; uranium in the economics of energy; role of high heat production granites in uranium province formation; and uranium deposits

Maximum temperature accounts for annual soil CO2 efflux in temperate forests of Northern China

Science.gov (United States)

Zhou, Zhiyong; Xu, Meili; Kang, Fengfeng; Jianxin Sun, Osbert

2015-01-01

It will help understand the representation legality of soil temperature to explore the correlations of soil respiration with variant properties of soil temperature. Soil temperature at 10 cm depth was hourly logged through twelve months. Basing on the measured soil temperature, soil respiration at different temporal scales were calculated using empirical functions for temperate forests. On monthly scale, soil respiration significantly correlated with maximum, minimum, mean and accumulated effective soil temperatures. Annual soil respiration varied from 409 g C m−2 in coniferous forest to 570 g C m−2 in mixed forest and to 692 g C m−2 in broadleaved forest, and was markedly explained by mean soil temperatures of the warmest day, July and summer, separately. These three soil temperatures reflected the maximum values on diurnal, monthly and annual scales. In accordance with their higher temperatures, summer soil respiration accounted for 51% of annual soil respiration across forest types, and broadleaved forest also had higher soil organic carbon content (SOC) and soil microbial biomass carbon content (SMBC), but a lower contribution of SMBC to SOC. This added proof to the findings that maximum soil temperature may accelerate the transformation of SOC to CO2-C via stimulating activities of soil microorganisms. PMID:26179467

EXTREME MAXIMUM AND MINIMUM AIR TEMPERATURE IN MEDİTERRANEAN COASTS IN TURKEY

Directory of Open Access Journals (Sweden)

Barbaros Gönençgil

2016-01-01

Full Text Available In this study, we determined extreme maximum and minimum temperatures in both summer and winter seasons at the stations in the Mediterranean coastal areas of Turkey.In the study, the data of 24 meteorological stations for the daily maximum and minimumtemperatures of the period from 1970–2010 were used. From this database, a set of four extreme temperature indices applied warm (TX90 and cold (TN10 days and warm spells (WSDI and cold spell duration (CSDI. The threshold values were calculated for each station to determine the temperatures that were above and below the seasonal norms in winter and summer. The TX90 index displays a positive statistically significant trend, while TN10 display negative nonsignificant trend. The occurrence of warm spells shows statistically significant increasing trend while the cold spells shows significantly decreasing trend over the Mediterranean coastline in Turkey.

Maximum And Minimum Temperature Trends In Mexico For The Last 31 Years

Science.gov (United States)

Romero-Centeno, R.; Zavala-Hidalgo, J.; Allende Arandia, M. E.; Carrasco-Mijarez, N.; Calderon-Bustamante, O.

2013-05-01

Based on high-resolution (1') daily maps of the maximum and minimum temperatures in Mexico, an analysis of the last 31-year trends is performed. The maps were generated using all the available information from more than 5,000 stations of the Mexican Weather Service (Servicio Meteorológico Nacional, SMN) for the period 1979-2009, along with data from the North American Regional Reanalysis (NARR). The data processing procedure includes a quality control step, in order to eliminate erroneous daily data, and make use of a high-resolution digital elevation model (from GEBCO), the relationship between air temperature and elevation by means of the average environmental lapse rate, and interpolation algorithms (linear and inverse-distance weighting). Based on the monthly gridded maps for the mentioned period, the maximum and minimum temperature trends calculated by least-squares linear regression and their statistical significance are obtained and discussed.

Thermodynamic and transport properties of uranium dioxide and related phases

International Nuclear Information System (INIS)

1965-01-01

The high melting point of uranium dioxide and its stability under irradiation have led to its use as a fuel in a variety of types of nuclear reactors. A wide range of chemical and physical studies has been stimulated by this circumstances and by the complex nature of the uranium dioxide phase itself. The boundaries of this phase widen as the temperature is increased; at 2000 deg. K a single, homogeneous phase exists from U 2.27 to a hypostoichiometric (UO 2-x ) composition, depending on the oxygen potential of the surroundings. Since there is often an incentive to operate a reactor at the maximum practicable heat rating and, therefore, maximum thermal gradient in the fuel, the determination of the physical properties of the UO 2-x phase becomes a matter of great technological importance. In addition a complex sequence of U-O phases may be formed during the preparation of powder feed material or during the sintering process; these affect the microstructure and properties of the final product and have also received much attention. 184 refs, 33 figs, 15 tabs

Thermal stress relieving of dilute uranium alloys

International Nuclear Information System (INIS)

Eckelmeyer, K.H.

1981-01-01

The kinetics of thermal stress relieving of uranium - 2.3 wt % niobium, uranium - 2.0 wt % molybdenum, and uranium - 0.75 wt % titanium are reported and discussed. Two temperature regimes of stress relieving are observed. In the low temperature regime (T 0 C) the process appears to be controlled by an athermal microplasticity mechanism which can be completely suppressed by prior age hardening. In the high temperature regime (300 0 C 0 C) the process appears to be controlled by a classical diffusional creep mechanism which is strongly dependent on temperature and time. Stress relieving is accelerated in cases where it occurs simultaneously with age hardening. The potential danger of residual stress induced stress corrosion cracking of uranium alloys is discussed

Trends in mean maximum temperature, mean minimum temperature and mean relative humidity for Lautoka, Fiji during 2003 – 2013

Directory of Open Access Journals (Sweden)

Syed S. Ghani

2017-12-01

Full Text Available The current work observes the trends in Lautoka’s temperature and relative humidity during the period 2003 – 2013, which were analyzed using the recently updated data obtained from Fiji Meteorological Services (FMS. Four elements, mean maximum temperature, mean minimum temperature along with diurnal temperature range (DTR and mean relative humidity are investigated. From 2003–2013, the annual mean temperature has been enhanced between 0.02 and 0.080C. The heating is more in minimum temperature than in maximum temperature, resulting in a decrease of diurnal temperature range. The statistically significant increase was mostly seen during the summer months of December and January. Mean Relative Humidity has also increased from 3% to 8%. The bases of abnormal climate conditions are also studied. These bases were defined with temperature or humidity anomalies in their appropriate time sequences. These established the observed findings and exhibited that climate has been becoming gradually damper and heater throughout Lautoka during this period. While we are only at an initial phase in the probable inclinations of temperature changes, ecological reactions to recent climate change are already evidently noticeable. So it is proposed that it would be easier to identify climate alteration in a small island nation like Fiji.

Study of natural thermoluminescence of quartzite in a gold and uranium mineralized zone (Canavieiras, Jacobina, Brazil)

International Nuclear Information System (INIS)

Ferreira, J.; Nordemann, D.

1976-01-01

The quartzite of the Canavieiras gold mine (Jacobina, Bahia, Brazil) exhibits a high temperature peak (280 +- 2) 0 C in its natural thermoluminescence glow curve. It was experimentally determined that the amount of light in this peak could be reproduced to within 5% for grain sizes between 80 and 100 mesh (0.149 and 0.177 mm). A positive correlation was found between the amount of this thermoluminescence and the uranium content with saturation beginning to be detected at the maximum (700 ppm) amount of uranium found. Assuming that the thermoluminescence peak used is at a temperature high enough to permit accumulation and stability at room temperatures, the thermoluminescence found could have accumulated in (12.1 +- 0.3) x 10 6 years. This may date a complete liberation of trapped electrons in conjunction with a well documented initiation of weathering. (author) [pt

Influence of pyrolytic temperature on uranium adsorption capability by biochar derived from macauba coconut residue

Energy Technology Data Exchange (ETDEWEB)

Guilhen, Sabine Neusatz; Fungaro, Denise Alves [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Coleti, Jorge; Tenório, Jorge Alberto Soares, E-mail: snguilhen@ipen.br, E-mail: dfungaro@ipen.br, E-mail: jorgecoleti@usp.br, E-mail: jtenorio@usp.br [Universidade de São Paulo (USP), São Paulo, SP (Brazil). Departamento de Engenharia Metalúrgica e de Materiais

2017-07-01

Biochar (BC) is a carbon-rich product obtained when biomass is thermally decomposed at relatively low temperatures (under 700°C) and limited supply of oxygen in a process called pyrolysis. The conversion of biomass into BC can not only result in renewable energy source of synthetic gas and bio-oil, but also decrease the content of CO{sub 2} in the atmosphere, as well as improving soil fertility. Because of its porous structure, charged surface and surface functional groups, BC exhibits a great potential as an adsorbent. Brazilian agro energy chain involves tons of biomass waste, providing a wide range of biomass with different chemical and physical properties. BC characteristics strongly depend on the feedstock and the pyrolysis conditions, in which the temperature is the key parameter. The aim of this study was to evaluate the adsorption potential for the removal of uranium, U(VI), from aqueous solutions using BC obtained through the pyrolysis of the Macauba (Acrocomia aculeata) coconut endocarp as a function of the final pyrolytic temperature. BCs produced at higher temperatures are likely to present lower H/C and O/C ratios, indicating the loss of easily degradable carbon compounds such as volatile matter. In contrast, low-temperature pyrolysis produces not only a higher BC yield, but also richer in surface functional groups which will likely enable interactions with the U(VI) ions. The endocarp was subjected to six different pyrolytic temperatures, ranging from 250°C to 750 °C. The influence of parameters such as pH, sorbent dose and initial concentration on the adsorption of U(VI) was investigated. The maximum adsorption capacity (q) was achieved for the BC obtained at 250°C (BC250), which presented a removal percentage of approx. 86%, demonstrating the potential of the BC from macauba endocarp for treatment of wastewaters. Thus, submitting the endocarp to temperatures higher than 250°C becomes unnecessary, saving time and reducing operating costs

Influence of pyrolytic temperature on uranium adsorption capability by biochar derived from macauba coconut residue

International Nuclear Information System (INIS)

Guilhen, Sabine Neusatz; Fungaro, Denise Alves; Coleti, Jorge; Tenório, Jorge Alberto Soares

2017-01-01

Biochar (BC) is a carbon-rich product obtained when biomass is thermally decomposed at relatively low temperatures (under 700°C) and limited supply of oxygen in a process called pyrolysis. The conversion of biomass into BC can not only result in renewable energy source of synthetic gas and bio-oil, but also decrease the content of CO 2 in the atmosphere, as well as improving soil fertility. Because of its porous structure, charged surface and surface functional groups, BC exhibits a great potential as an adsorbent. Brazilian agro energy chain involves tons of biomass waste, providing a wide range of biomass with different chemical and physical properties. BC characteristics strongly depend on the feedstock and the pyrolysis conditions, in which the temperature is the key parameter. The aim of this study was to evaluate the adsorption potential for the removal of uranium, U(VI), from aqueous solutions using BC obtained through the pyrolysis of the Macauba (Acrocomia aculeata) coconut endocarp as a function of the final pyrolytic temperature. BCs produced at higher temperatures are likely to present lower H/C and O/C ratios, indicating the loss of easily degradable carbon compounds such as volatile matter. In contrast, low-temperature pyrolysis produces not only a higher BC yield, but also richer in surface functional groups which will likely enable interactions with the U(VI) ions. The endocarp was subjected to six different pyrolytic temperatures, ranging from 250°C to 750 °C. The influence of parameters such as pH, sorbent dose and initial concentration on the adsorption of U(VI) was investigated. The maximum adsorption capacity (q) was achieved for the BC obtained at 250°C (BC250), which presented a removal percentage of approx. 86%, demonstrating the potential of the BC from macauba endocarp for treatment of wastewaters. Thus, submitting the endocarp to temperatures higher than 250°C becomes unnecessary, saving time and reducing operating costs. (author)

In-situ neutron diffraction characterization of temperature dependence deformation in α-uranium

Science.gov (United States)

Calhoun, C. A.; Garlea, E.; Sisneros, T. A.; Agnew, S. R.

2018-04-01

In-situ strain neutron diffraction measurements were conducted at temperature on specimens coming from a clock-rolled α-uranium plate, and Elasto-Plastic Self-Consistent (EPSC) modeling was employed to interpret the findings. The modeling revealed that the active slip systems exhibit a thermally activated response, while deformation twinning remains athermal over the temperature ranges explored (25-150 °C). The modeling also allowed assessment of the effects of thermal residual stresses on the mechanical response during compression. These results are consistent with those from a prior study of room-temperature deformation, indicating that the thermal residual stresses strongly influence the internal strain evolution of grain families, as monitored with neutron diffraction, even though accounting for these residual stresses has little effect on the macroscopic flow curve, except in the elasto-plastic transition.

Influence of uranium hydride oxidation on uranium metal behaviour

International Nuclear Information System (INIS)

Patel, N.; Hambley, D.; Clarke, S.A.; Simpson, K.

2013-01-01

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

Influence of uranium hydride oxidation on uranium metal behaviour

Energy Technology Data Exchange (ETDEWEB)

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

2013-07-01

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

New England observed and predicted growing season maximum stream/river temperature points

Data.gov (United States)

U.S. Environmental Protection Agency — The shapefile contains points with associated observed and predicted growing season maximum stream/river temperatures in New England based on a spatial statistical...

Equations of state for enriched uranium and uranium alloy to 3500 MPa

International Nuclear Information System (INIS)

Bai Chaomao; Hai Yuying; Liu Jenlong; Li Zhenrong

1990-04-01

The volume compressions of 6 kinds of cast materials including enriched uranium, poor uranium, U-0.57 wt% Ti, U-0.33 wt% Nb, U-2.85 wt% Nb and U-7.5 wt% Nb-3.3 wt% Zr have been determined by monitoring piston displacements in a piston cylinder apparatus with double strengthening rings to 3500 MPa at room temperature. The dilation of the cylinder vessel and the press deformation were corrected by some experiments. The calculational data free from using the standard sample closed with used standard sample. The volume compressions of enriched uranium and poor uranium are nearly coincident. Pure uranium is more compressible than uranium alloys. These values of enriched uranium are in close agreement with values of Bridgman's pure uranium. The fitting coefficients of Bridgman's polynomial and Anderson's equation of state and isothermal bulk modules for the above materials are given

Study of the recrystallisation of irradiated uranium; Etude sur l'uranium irradie

Energy Technology Data Exchange (ETDEWEB)

Bloch, J; Mustelier, J P; Bussy, P; Blin, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1958-07-01

1- Study of the recrystallisation of irradiated uranium. The recrystallisation of uranium irradiated to a burnup level of 220 MWj/t, at a temperature of the order of 350 deg. C, has been investigated. The observations were made chiefly by means of micrography an hardness measurements. If the irradiated metal is compared with a cold-drawn metal showing the same shearing of the twinned crystals, and therefore the same rate of plastic deformation, as the irradiated metal, it is noted that the restoring of the irradiated metal takes place at a considerably higher temperature than that of the cold-drawn metal. Pre-crystallisation is very much delayed. Only, a passage of the {alpha}-{beta} transformation point quickly wipes out irradiation effect. 2- Hardening of uranium by irradiation. Using hardness measurements we have studied more especially the effect of very weak irradiations on uranium (integrated flux < 10{sup 16} nvt). The hardness does not increase linearly with the flux, but a period of incubation is observed probably representing the time necessary for saturation of the dislocations. (author)Fren. [French] 1- Etude de la recristallisation de l'uranium irradie. On a etudie la recristallisation d'uranium irradie jusqu'a un taux de combustion de 220 MWj/t a une temperature de l'ordre de 350 deg. C. Les observations ont ete faites principalement a l'aide de la micrographie et de la durete. Si l'on compare le metal irradie avec un metal ecroui presentant le meme cisaillement des macles, donc le meme taux de deformation plastique que le metal irradie, on constate que la restauration du metal irradie se fait a une temperature notablement superieure a celle du metal ecroui. La recristallisation est tres retardee. Seul, un passage du point de transformation {alpha}-{beta} efface rapidement l'effet de l'irradiation. 2- Durcissement de l'uranium par irradiation. Nous avons, a l'aide de la durete, etudie plus particulierement l'effet de tres faibles irrtions sur l'uranium

Plastic Flow Characteristics of Uranium-Niobium as a Function of Strain Rate and Temperature

International Nuclear Information System (INIS)

Cady, C.M.; Gray, G.T. III; Hecker, S.S; Thoma, D.J.; Korzekwa, D.R.; Patterson, R.A.; Dunn, P.S.; Bingert, J.F.

1999-01-01

The stress-strain response of uranium-niobium alloys as a function of temperature, strain-rate and stress-state was investigated. The yield and flow stresses of the U-Nb alloys were found to exhibit a pronounced strain rate sensitivity, while the hardening rates were found to be insensitive to strain rate and temperature. The overall stress-strain response of the U-6Nb exhibits a sinusoidal hardening response, which is consistent with multiple deformation modes and is thought to be related to shape-memory behavior

Uranium and other heavy metal resistance and accumulation in bacteria isolated from uranium mine wastes.

Science.gov (United States)

Choudhary, Sangeeta; Islam, Ekramul; Kazy, Sufia K; Sar, Pinaki

2012-01-01

Ten bacterial strains isolated from uranium mine wastes were characterized in terms of their uranium and other metal resistance and accumulation. 16S rRNA gene sequence analysis identified the strains as members of genera Bacillus, Serratia, and Arthrobacter. Strains were able to utilize various carbon sources, particularly aromatic hydrocarbons, grow at broad pH and temperature ranges and produce non specific acid phosphatase relevant for metal phosphate precipitation in contaminated environment. The isolates exhibited high uranium and other heavy metals (Ni, Co, Cu and Cd) resistance and accumulation capacities. Particularly, Arthrobacter sp. J001 and Bacillus sp. J003 were superior in terms of U resistance at low pH (pH 4.0) along with metals and actinides (U and Th) removal with maximum cell loading of 1088 μmol U, 1293 μmol Th, 425 μmol Cu, 305 μmol Cd, 377 μmol Zn, 250 μmol Ni g(-1) cell dry wt. Genes encoding P(1B)-type ATPases (Cu-CPx and Zn-CPx) and ABC transporters (nik) as catalytic tools for maintaining cellular metal homeostasis were detected within several Bacillus spp., with possible incidence of horizontal gene transfer for the later gene showing phylogenetic lineage to α Proteobacteria members. The study provides evidence on intrinsic abilities of indigenous bacteria from U-mine suitable for survival and cleaning up of contaminated mine sites.

The fracture mechanism of uranium-niobium alloys near hypoeutectoid composition aged at low temperature

International Nuclear Information System (INIS)

Wang Xiaoying; Ren Dapeng; Yang Jianxiong; Jiang Guifen

2006-01-01

The microstructures and the crack propagation of uranium-niobium alloys near hypoeutectoid composition aged at temperature 200 degree C for 2 hours during a tension was investigated by means of in situ tension tests using TEM. The results show that the twinning planes inside and between the martensite laths move and merge, and then disintegrate in uranium-niobium alloys with monoclinic α structure during the tension. The crack propagation can be described as follows. Under the tension, the thinning zone which is locally plastically deformed emerges in the front of the crack tip. After the process of nucleation, growth and conjunction, the microvoids connect with the main crack, which results in the fracture. Neither of emission, propagation and movement of dislocation was observed during the tension. (authors)

Radiation damage of metal uranium

International Nuclear Information System (INIS)

Mihajlovic, A.

1965-01-01

This report is concerned with the role of dispersion second phase in uranium and burnup rate. The role of dispersion phases in radiation stability of metal uranium was studies by three methods: variation of electric conductivity dependent on the neutron flux and temperature of pure uranium for different states of dispersion second phase; influence of dispersion phase on the radiation creep; transmission electron microscopy of fresh and irradiated uranium

Uranium extraction history using pressure leaching

International Nuclear Information System (INIS)

Fraser, K.S.; Thomas, K.G.

2010-01-01

Over the past 60 years of uranium process development only a few commercial uranium plants have adopted a pressure leaching process in their flowsheet. The selection of acid versus alkaline pressure leaching is related to the uranium and gangue mineralogy. Tetravalent (U"+"4) uranium has to be oxidized to hexavalent (U"+"6) uranium to be soluble. Refractory tetravalent uranium requires higher temperature and pressure, as practised in pressure leaching, for conversation to soluble hexavalent uranium. This paper chronicles the history of these uranium pressure leaching facilities over the past 60 years, with specific details of each design and operation. (author)

Effect of glycine, DL-alanine and DL-2-aminobutyric acid on the temperature of maximum density of water

International Nuclear Information System (INIS)

Romero, Carmen M.; Torres, Andres Felipe

2015-01-01

Highlights: • Effect of α-amino acids on the temperature of maximum density of water is presented. • The addition of α-amino acids decreases the temperature of maximum density of water. • Despretz constants suggest that the amino acids behave as water structure breakers. • Despretz constants decrease as the number of CH 2 groups of the amino acid increase. • Solute disrupting effect becomes smaller as its hydrophobic character increases. - Abstract: The effect of glycine, DL-alanine and DL-2-aminobutyric acid on the temperature of maximum density of water was determined from density measurements using a magnetic float densimeter. Densities of aqueous solutions were measured within the temperature range from T = (275.65 to 278.65) K at intervals of T = 0.50 K over the concentration range between (0.0300 and 0.1000) mol · kg −1 . A linear relationship between density and concentration was obtained for all the systems in the temperature range considered. The temperature of maximum density was determined from the experimental results. The effect of the three amino acids is to decrease the temperature of maximum density of water and the decrease is proportional to molality according to Despretz equation. The effect of the amino acids on the temperature of maximum density decreases as the number of methylene groups of the alkyl chain becomes larger. The results are discussed in terms of (solute + water) interactions and the effect of amino acids on water structure

Solid phase extraction of uranium(VI) onto benzoylthiourea-anchored activated carbon

International Nuclear Information System (INIS)

Zhao Yongsheng; Liu Chunxia; Feng Miao; Chen Zhen; Li Shuqiong; Tian Gan; Wang Li; Huang Jingbo; Li Shoujian

2010-01-01

A new solid phase extractant selective for uranium(VI) based on benzoylthiourea anchored to activated carbon was developed via hydroxylation, amidation and reaction with benzoyl isothiocyanate in sequence. Fourier transform infrared spectroscopy and total element analysis proved that benzoylthiourea had been successfully grafted to the surface of the activated carbon, with a loading capacity of 1.2 mmol benzoylthiourea per gram of activated carbon. The parameters that affect the uranium(VI) sorption, such as contact time, solution pH, initial uranium(VI) concentration, adsorbent dose and temperature, have been investigated. Results have been analyzed by Langmuir and Freundlich isotherm; the former was more suitable to describe the sorption process. The maximum sorption capacity (82 mg/g) for uranium(VI) was obtained at experimental conditions. The rate constant for the uranium sorption by the as-synthesized extractant was 0.441 min -1 from the first order rate equation. Thermodynamic parameters (ΔH 0 = -46.2 kJ/mol; ΔS 0 = -98.0 J/mol K; ΔG 0 = -17.5 kJ/mol) showed the adsorption of an exothermic process and spontaneous nature, respectively. Additional studies indicated that the benzoylthiourea-anchored activated carbon (BT-AC) selectively sorbed uranyl ions in the presence of competing ions, Na + , Co 2+ , Sr 2+ , Cs + and La 3+ .

Uranium recovering from slags generated in the metallic uranium by magnesiothermic reduction

International Nuclear Information System (INIS)

Fornarolo, F.; Carvalho, E.F. Urano de; Durazzo, M.; Riella, H.G.

2008-01-01

The Nuclear Fuel Center of IPEN/CNEN-SP has recent/y concluded a program for developing the fabrication technology of the nuclear fuel based on the U 3 Si 2 -Al dispersion, which is being used in the IEA-R1 research reactor. The uranium silicide (U 3 Si 2 ) fuel production starts with the uranium hexafluoride (UF 6 ) processing and uranium tetrafluoride (UF 4 ) precipitation. Then, the UF 4 is converted to metallic uranium by magnesiothermic reduction. The UF 4 reduction by magnesium generates MgF 2 slag containing considerable concentrations of uranium, which could reach 20 wt%. The uranium contained in that slag should be recovered and this work presents the results obtained in recovering the uranium from that slag. The uranium recovery is accomplished by acidic leaching of the calcined slag. The calcination transforms the metallic uranium in U 3 O 8 , promoting the pulverization of the pieces of metallic uranium and facilitating the leaching operation. As process variables, have been considered the nitric molar concentration, the acid excess regarding the stoichiometry and the leaching temperature. As result, the uranium recovery reached a 96% yield. (author)

Thermodynamic properties of α-uranium

International Nuclear Information System (INIS)

Ren, Zhiyong; Wu, Jun; Ma, Rong; Hu, Guichao; Luo, Chao

2016-01-01

The lattice constants and equilibrium atomic volume of α-uranium were calculated by Density Functional Theory (DFT). The first principles calculation results of the lattice for α-uranium are in agreement with the experimental results well. The thermodynamic properties of α-uranium from 0 to 900 K and 0–100 GPa were calculated with the quasi-harmonic Debye model. Volume, bulk modulus, entropy, Debye temperature, thermal expansion coefficient and the heat capacity of α-uranium were calculated. The calculated results show that the bulk modulus and Debye temperature increase with the increasing pressure at a given temperature while decreasing with the increasing temperature at a given pressure. Volume, entropy, thermal expansion coefficient and the heat capacity decrease with the increasing pressure while increasing with the increasing temperature. The theoretical results of entropy, Debye temperature, thermal expansion coefficient and the heat capacity show good agreement with the general trends of the experimental values. The constant-volume heat capacity shows typical Debye T"3 power-law behavior at low temperature limit and approaches to the classical asymptotic Dulong-Petit limit at high temperature limit. - Highlights: • Thermodynamic properties of α-U were predicted systematically with quasi-harmonic Debye model. • Summarizations of the corresponding experimental and theoretical results have been made for the EOS and other thermodynamic parameters. • The calculated thermodynamic properties show good agreement with the experimental results in general trends.

Thermodynamic properties of α-uranium

Energy Technology Data Exchange (ETDEWEB)

Ren, Zhiyong; Wu, Jun; Ma, Rong; Hu, Guichao; Luo, Chao, E-mail: luochaoboss@sohu.com

2016-11-15

The lattice constants and equilibrium atomic volume of α-uranium were calculated by Density Functional Theory (DFT). The first principles calculation results of the lattice for α-uranium are in agreement with the experimental results well. The thermodynamic properties of α-uranium from 0 to 900 K and 0–100 GPa were calculated with the quasi-harmonic Debye model. Volume, bulk modulus, entropy, Debye temperature, thermal expansion coefficient and the heat capacity of α-uranium were calculated. The calculated results show that the bulk modulus and Debye temperature increase with the increasing pressure at a given temperature while decreasing with the increasing temperature at a given pressure. Volume, entropy, thermal expansion coefficient and the heat capacity decrease with the increasing pressure while increasing with the increasing temperature. The theoretical results of entropy, Debye temperature, thermal expansion coefficient and the heat capacity show good agreement with the general trends of the experimental values. The constant-volume heat capacity shows typical Debye T{sup 3} power-law behavior at low temperature limit and approaches to the classical asymptotic Dulong-Petit limit at high temperature limit. - Highlights: • Thermodynamic properties of α-U were predicted systematically with quasi-harmonic Debye model. • Summarizations of the corresponding experimental and theoretical results have been made for the EOS and other thermodynamic parameters. • The calculated thermodynamic properties show good agreement with the experimental results in general trends.

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

Reaction of uranium and the fluorocarbon FC-75

Science.gov (United States)

Young, R. H.

1985-04-01

Because of criticality concerns with water cooling in enriched uranium upgrading, a fluorocarbon has been evaluated as a replacement coolant for internal module components in the Plasma Separation Process (PSP). The interaction of bulk uranium and of powdered uranium with FC-75 has been investigated at temperatures between 200 and 700 C. The gas pressure and the metal temperature were monitored as a function of time. Modest temperature changes of 50 to 100 C were observed for the bulk uranium/fluorocarbon reaction. Much larger changes (up to 1000 C) were noted for the reaction involving high surface area uranium powder. These temperature transients, particularly for the powdered uranium reaction, were short-lived ( 10 seconds) and indicative of the formation of a protective layer of reaction products. Analysis of residual gas products by infrared spectroscopy indicated that one potentially serious hazard, UF6, was not present; however, several small toxic fluorocarbons were produced by thermolysis and/or reaction. X-ray diffraction analysis of the residual solids indicated UF4 and UO2 were the major solid products.

Granite-related hypothermal uranium mineralization in South China

International Nuclear Information System (INIS)

Liu, X.; Wu, J.; Pan, J.; Zhu, M.

2014-01-01

As one of the important geological types, granite-related uranium deposits account for about 29% of the total discovered natural uranium resources in China. Most of the granite-related uranium deposits located in Taoshan - Zhuguang uranium metallogenic belt, South China. In addition to the typical pitchblende vein-type uranium mineralization of epithermal metallogenic system, a new type of granite-related uranium mineralization with characteristics of hypothermal matallogenic system was discovered in South China by current studies. However, hypothermal is contact thermal to epithermal mineralization, and not the conventional intrusive high temperature mineralization. Hypothermal uranium mineralization is presented by disseminated uraninite or pitchblende stockwork in fissures in granites normally with extensive alkaline alteration. The high temperature mineral assemblage of uraninite associate with scheelite and tourmaline was identified in hypothermal uranium mineralization. Fluid inclusion studies on this type mineralization indicated the middle to high temperature (>250℃) mineralization with the mixing evidence of ore forming solution derived from deep level, and the boiling and mixing of ore forming solution are regarded as the dominant mineralization mechanism for the precipitating of uranium. In contrast to the mineralization ages of 67 Ma to 87 Ma for typical pitchblende vein mineralization of epithermal metallogenic system, the mineralization age is older than 100 Ma for hypothermal uranium mineralization in granite. In the Shituling deposit, Xiazhuang uranium ore field, uraninite and pitchblende micro veins with extensive potassic alteration, chloritization and sericitization are hosted in fissures of Indo-Chinese epoch granites with the uranium mineralization age of 130 Ma to 138 Ma with a mineralization temperature of 290℃ to 330℃ indicated. Other examples sharing the similar characters of hypothermal uranium mineralization have been recognized in

Studies on some influential factors of the zinc-activated carbon composite adsorbent on adsorptivity for uranium

International Nuclear Information System (INIS)

Miyai, Yoshitaka; Kitamura, Takao; Takagi, Norio; Katoh, Shunsaku; Miyazaki, Hidetoshi

1978-01-01

Factors, which influence the uranium adsorption of powdery composite adsorbent of basic zinc carbonate and activated carbon were studied. In the range studied, zinc content of the adsorbent was the most influential factor on the uranium adsorption, and the second influential factor was sea water volume and the third factor was adsorption period. Interactive effects were observed between zinc content and sea water volume, and between zinc content and adsorption period, and it was deduced that there existed the optimum value of sea water volume and adsorption period respectively for the zinc content of the adsorbent. Maximum uranium adsorption of adsorbent with 40% zinc content was observed at sea water volume of 15 liters and adsorption period of 25 hrs. As for temperature in the range of 15 - 35 0 C, the lower the temperature, the larger amount of adsorbed uranium was. The powdery adsorbent was made into granule, and its strength and its uranium adsorptivity were studied in relation to the granulating conditions. By use of PVA with degree of polymerization above 1,700 as binder, the granular adsorbent with the same strength as commercial granular activated carbon was obtained. PVA amount and its degree of polymerization gave only small effect on uranium adsorption of the adsorbent. Effect of granule size on the uranium adsorption rate in the range of 1 - 4 mm was that the uranium adsorption rate changed proportionally to surface area of assumed sphere. As a test for practical use, five times repetitions of adsorption and desorption were carried out on the same granular adsorbent. During the repetition the amount of adsorbed uranium rather increased, and desorption ratio of adsorbed uranium was constant at 91 - 93%. The weight loss of the adsorbent in a cycle of adsorption and desorption was about 3%. (author)

Thermal stress relieving of dilute uranium alloys

International Nuclear Information System (INIS)

Eckelmeyer, K.H.

1980-01-01

The kinetics of thermal stress relieving of uranium - 2.3 wt. % niobium, uranium - 2.0 wt. % molybdenum, and uranium - 0.75 wt. % titanium are reported and discussed. Two temperature regimes of stress relieving are observed. In the low temperature regime (T 0 C) the process appears to be controlled by an athermal microplasticity mechanism which can be completely suppressed by prior age hardening. In the high temperature regime (300 0 C 0 C) the process appears to be controlled by a classical diffusional creep mechanism which is strongly dependent on temperature and time. Stress relieving is accelerated in cases where it occurs simultaneously with age hardening. The potential danger of residual stress induced stress corrosion cracking of uranium alloys is discussed. It is shown that the residual stress relief which accompanies age hardening of uranium - 0.75% titanium more than compensates for the reduction in K/sub ISCC/ caused by aging. As a result, age hardening actually decreases the susceptibility of this alloy to residual stress induced stress corrosion cracking

Electrochemical preparation of new uranium oxide phases

International Nuclear Information System (INIS)

Smolenskij, V.V.; Lyalyushkin, N.V.; Bove, A.L.; Komarov, V.K.; Kapshukov, I.I.

1992-01-01

Behaviour of uranium ions in oxidation states 3+ and 4+ in molten chlorides of alkali metals in the temperature range of 700-900 degC in the atmosphere of an inert gas was studied by the method of cyclic voltametry. It is shown that as a result of introduction of crystal uranium dioxide into the salt melt formation of uranium oxide ions of the composition UO + and UO 2+ occurs, the ions participating in electrode reactions and bringing about formation of the following uranium oxides on the cathode: UO and, presumably, U 3 O 4 . Oxides UO and U 3 O 4 are thermodynamically unstable at low temperatures and decompose into uranium oxide of the composition UO 2-x , where x varies from 0 to 0.05, and metal uranium

Uranium self-diffusion in uranium monocarbide; Determination du coefficient d'autodiffusion de l'uranium dans son monocarbure

Energy Technology Data Exchange (ETDEWEB)

Villaine, P [Commissariat a l' Energie Atomique, 38 - Grenoble (France). Centre d' Etudes Nucleaires

1967-10-01

Uranium self diffusion in near-stoichiometric stabilized uranium monocarbide has been investigated in the temperature range 1450-2000 deg. C. A thin layer of {sup 235}UC was deposited onto the samples and the diffusion profiles were analyzed by both sectioning and alpha-spectrometry techniques. The variation with temperature of the self-diffusion coefficient can be expressed by the equation: D = 7.5 x 10{sup -5} exp [-(81 {+-} 10) kcal/mole / RT] Cm{sup 2} s{sup -1} The coefficient D decreases with increasing carbon content. Autoradiographs and profile analysis have evidenced a preferential grain-boundary diffusion at all temperatures and compositions investigated. This phenomenon was used for a study of grain-boundary migration and for the evaluation of grain-boundary diffusion coefficients. The activation energy thus derived is close to the volume diffusion activation energy. (author) [French] L'autodiffusion de l'uranium dans le monocarbure d'uranium de composition voisine de la stoechiometrie et stabilise par recuit prealable, a ete etudiee entre 1450 et 2000 deg. C par la methode du depot mince de traceur, suivie des techniques d'abrasion comptage et de spectrometrie alpha. La variation avec la temperature du coefficient d'autodiffusion peut s'ecrire: D = 7.5 x 10{sup -5} exp [-(81 {+-} 10) kcal/mole / RT] Cm{sup 2} s{sup -1} Le coefficient D decroit avec une augmentation de la teneur en carbone. L'observation d'autoradiographies et l'analyse de profils de diffusion ont mis en evidence l'importance d'une diffusion intergranulaire preferentielle pour toutes les compositions etudiees et a toutes les temperatures. Cette diffusion a egalement ete utilisee pour l'etude de la migration des joints de grains et pour le calcul approche du coefficient de diffusion mtergranulaire. L'energie d'activation ainsi determinee est voisine de celle correspondant a la diffusion volumique. (auteur)

PRODUCTION OF URANIUM METAL BY CARBON REDUCTION

Science.gov (United States)

Holden, R.B.; Powers, R.M.; Blaber, O.J.

1959-09-22

The preparation of uranium metal by the carbon reduction of an oxide of uranium is described. In a preferred embodiment of the invention a charge composed of carbon and uranium oxide is heated to a solid mass after which it is further heated under vacuum to a temperature of about 2000 deg C to produce a fused uranium metal. Slowly ccoling the fused mass produces a dendritic structure of uranium carbide in uranium metal. Reacting the solidified charge with deionized water hydrolyzes the uranium carbide to finely divide uranium dioxide which can be separated from the coarser uranium metal by ordinary filtration methods.

The Streltsovskoye uranium district

International Nuclear Information System (INIS)

Ischukova, L.P.

1997-01-01

This paper describes the geology of the Streltsovskoye uranium district located in south-eastern Zabaikalie region, Chita Province, Siberia, Russia. This district hosts Russia's only currently active uranium production centre. The uranium ore was discovered from 1963 to 1967 by drilling below fluorite veins which had minor associated uranium mineralization and radioactive anomalies. The uranium occurs as large scale vein stockwork deposits of hydrothermal origin within a volcano-tectonic caldera formed by continental volcanism of Late Mesozoic age. Rocks occurring in the caldera include basalt and trachydacite, overlain by rhyolite, and with associated interbedded sediments. The ore bodies occur in steeply dipping faults, with the greatest concentrations located where faults along the margins of the caldera intersect steeply dipping, cross cutting, northeasterly and northwesterly striking faults. The Streltsovskoye caldera extends over an area of 150 km 2 and is underlain by a large batholith. The 19 identified uranium deposits occurred in structural features that cut through the caldera sequence and extend into the basement rocks. The caldera has a maximum thickness of 1400 metres. Details of several deposits are given, including descriptions of mineralization and associated alteration. (author). 10 figs

Measurement of the temperature of density maximum of water solutions using a convective flow technique

OpenAIRE

Cawley, M.F.; McGlynn, D.; Mooney, P.A.

2006-01-01

A technique is described which yields an accurate measurement of the temperature of density maximum of fluids which exhibit such anomalous behaviour. The method relies on the detection of changes in convective flow in a rectangular cavity containing the test fluid.The normal single-cell convection which occurs in the presence of a horizontal temperature gradient changes to a double cell configuration in the vicinity of the density maximum, and this transition manifests itself in changes in th...

The effects of types of media on uranium leaching using metabolite of Aspergillus niger

International Nuclear Information System (INIS)

Li Guangyue; Ding Dexin; Wang Yongdong; Hu Nan

2012-01-01

To investigate the influences of different media to uranium leaching applying with metabolite of Aspergillus niger, PSA and glucose-steepwater medium were used for the culture of Aspergillus niger, and the metabolite of Aspergillus niger with different pH value produced in the diverse culture temperature were obtained which was applied on the tests of uranium leaching as leaching agent. The test results show that the maximum leaching rate is 83.05% when the leaching agent is the metabolite of Aspergillus niger produced by PSA, as for the glucose- steepwater medium, the maximum leaching rate is 68.20%. The pH value of the metabolite of Aspergillus niger of the two kinds of media has a significant effect on the leaching rate. When PSA is adopted, the best leaching rate appears at the pH value of metabolite ranging from 2.0 to 2.5, and as for the glucose-steepwater medium, the pH value is below 2.1. (authors)

Uranium geochemistry on the Amazon shelf: Evidence for uranium release from bottom sediments

International Nuclear Information System (INIS)

McKee, B.A.; DeMaster, D.J.; Nittrouer, C.A.

1987-01-01

In Amazon-shelf waters, as salinity increases to 36.5 x 10 -3 , dissolved uranium activities increase to a maximum of 4.60 dpm 1 -1 . This value is much higher than the open-ocean value (2.50 dpm 1 -1 ), indicating a source of dissolved uranium to shelf waters in addition to that supplied from open-ocean and riverine waters. Uranium activities are much lower for surface sediments in the Amazon-shelf sea bed (mean: 0.69 ± .09 dpm g -1 ) than for suspended sediments in the Amazon river (1.82 dpm g -1 ). Data suggest that the loss of particulate uranium from riverine sediments is probably the result of uranium desorption from the ferric-oxyhydroxide coatings on sediment particles, and/or uranium release by mobilization of the ferric oxyhydroxides. The total flux of dissolved 238 U from the Amazon shelf (about 1.2 x 10 15 dpm yr -1 ) constitutes about 15% of uranium input to the world ocean, commensurate to the Amazon River's contribution to world river-water discharge. Measurement of only the riverine flux of dissolved 238 U underestimates, by a factor of about 5, the flux of dissolved 238 U from the Amazon shelf to the open ocean

Adsorption property of Br-PADAP-impregnated multiwall carbon nanotubes towards uranium and its performance in the selective separation and determination of uranium in different environmental samples.

Science.gov (United States)

Khamirchi, Ramzanali; Hosseini-Bandegharaei, Ahmad; Alahabadi, Ahmad; Sivamani, Selvaraju; Rahmani-Sani, Abolfazl; Shahryari, Taher; Anastopoulos, Ioannis; Miri, Mohammad; Tran, Hai Nguyen

2018-04-15

A newer efficient U(VI) ion adsorbent was synthesized by impregnating Br-PADAP [2-(5-Bromo-2-pyridylazo)-5-(diethylamino)phenol] onto multiwall carbon nanotubes (MWCNTs). The effects of various operation conditions on uranium adsorption (i.e., pH contact time, temperature, and initial uranium concentration) were systematically evaluated using batch experiments. The results indicated that the uranium adsorption on modified MWNCTs (5.571 × 10 -3 g/mg × min) reached faster equilibrium than that on pristine MWNCTs (4.832 × 10 -3 g/mg × min), reflecting the involvement of appropriate functional groups of Br-PADAP on the chelating ion-exchange mechanism of U(VI) adsorption. Modified MWNCTs (83.4mg/g) exhibited significantly higher maximum Langmuir adsorption capacity than pristine MWNCTs (15.1mg/g). Approximately 99% of uranium adsorbed onto modified MWNCTs can be desorbed by 2.5mL of 1M HNO 3 solution. Therefore, Br-PADAP-modified MWNCTs can server as a promising adsorbent for efficient uranium adsorption applications in water treatment. Subsequently, the proposed solid-phase extraction (using a mini-column packed with Br-PADAP/MWCNT) was successfully utilized for analysing trace uranium levels by the ICP-AES method in different environmental samples with a pre-concentration factor of 300-fold. The coexistence of other ions demonstrated an insignificant interference on the separative pre-concentration of uranium. the detection limit was recognized as 0.14μg/L, and the relative standard deviation was approximately 3.3% (n = 7). Copyright © 2017 Elsevier Inc. All rights reserved.

Synthesis of Uranium nitride powders using metal uranium powders

International Nuclear Information System (INIS)

Yang, Jae Ho; Kim, Dong Joo; Oh, Jang Soo; Rhee, Young Woo; Kim, Jong Hun; Kim, Keon Sik

2012-01-01

Uranium nitride (UN) is a potential fuel material for advanced nuclear reactors because of their high fuel density, high thermal conductivity, high melting temperature, and considerable breeding capability in LWRs. Uranium nitride powders can be fabricated by a carbothermic reduction of the oxide powders, or the nitriding of metal uranium. The carbothermic reduction has an advantage in the production of fine powders. However it has many drawbacks such as an inevitable engagement of impurities, process burden, and difficulties in reusing of expensive N 15 gas. Manufacturing concerns issued in the carbothermic reduction process can be solved by changing the starting materials from oxide powder to metals. However, in nitriding process of metal, it is difficult to obtain fine nitride powders because metal uranium is usually fabricated in the form of bulk ingots. In this study, a simple reaction method was tested to fabricate uranium nitride powders directly from uranium metal powders. We fabricated uranium metal spherical powder and flake using a centrifugal atomization method. The nitride powders were obtained by thermal treating those metal particles under nitrogen containing gas. We investigated the phase and morphology evolutions of powders during the nitriding process. A phase analysis of nitride powders was also a part of the present work

Dissolution of metallic uranium and its alloys. Part II. Screening study results: Identification of an effective non-thermal uranium dissolution method

International Nuclear Information System (INIS)

Laue, C.A.; Gates-Anderson, D.; Fitch, T.E.

2004-01-01

Screening experiments were performed to evaluate reagent systems that deactivate pyrophoric, metallic depleted uranium waste streams at ambient temperature. The results presented led to the selection of two systems, which would be investigated further, for the design of the LLNL onsite treatment process of metallic depleted uranium wastes. The two feasible systems are: (a) 7.5 mol/l H 2 SO 4 - 1 mol/l HNO 3 and (b) 3 mol/l HCl - 1 mol/l H 3 PO 4 . The sulfuric acid system dissolves uranium metal completely, while the hydrochloric-phosphoric acid system converts the metal completely into a solid, which might be suitable for direct disposal. Both systems combine oxidation of metallic uranium with complexation of the uranium ions formed to effectively deactivate uranium.s pyrophoricity at ambient temperature. (author)

Device for determining the maximum temperature of an environment

International Nuclear Information System (INIS)

Cartier, Louis.

1976-01-01

This invention concerns a device for determining the maximum temperature of an environment. Its main characteristic is a central cylindrical rod on which can slide two identical tubes, the facing ends of which are placed end to end and the far ends are shaped to provide a sliding friction along the rod. The rod and tubes are fabricated in materials of which the linear expansion factors are different in value. The far ends are composed of tongs of which the fingers, fitted with claws, bear on the central rod. Because of this arrangement of the device the two tubes, placed end to end on being fitted, can expand under the effect of a rise in the temperature of the environment into which the device is introduced, with the result that there occurs an increase in the distance between the two far ends. This distance is maximal when the device is raised to its highest temperature. The far ends are shaped to allow the tubes to slide under the effect of expansion but to prevent sliding in the opposite direction when the device is taken back into the open air and the temperature drops to within ambient temperature. It follows that the tubes tend to return to their initial length and the ends that were placed end to end when fitted now have a gap between them. The measurement of this gap makes it possible to know the maximal temperature sought [fr

Drawing of uranium in {gamma} phase; Filage de l'uranium en phase gamma

Energy Technology Data Exchange (ETDEWEB)

Stohr, J A [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires; Chevigny, R [Conpagnie, Pechiney, 73 - Chambery (France)

1955-07-01

It describes the study of working and drawing of uranium in {gamma} phase. In a first part, the forgeable characteristics of uranium metal in the three different phases ({alpha}, {beta} and {gamma}) are compared by using BASTIEN-PORTEVIN method. The different experiments are testing the behaviour metal in each phase under different stresses and a temperature gradient as slow and shock traction, slow and shock compression, resilience, flexibility. Results show that optimum conditions for uranium drawing is uranium in phase {gamma}. In a second part, it described the drawing method and process. The uranium rods obtained by this technique are of very good quality. In addition, the material wear is very low which permits a low production cost. Finally, the uranium rod physical properties are studied. (M.P.)

Production of uranium dioxide

International Nuclear Information System (INIS)

Hart, J.E.; Shuck, D.L.; Lyon, W.L.

1977-01-01

A continuous, four stage fluidized bed process for converting uranium hexafluoride (UF 6 ) to ceramic-grade uranium dioxide (UO 2 ) powder suitable for use in the manufacture of fuel pellets for nuclear reactors is disclosed. The process comprises the steps of first reacting UF 6 with steam in a first fluidized bed, preferably at about 550 0 C, to form solid intermediate reaction products UO 2 F 2 , U 3 O 8 and an off-gas including hydrogen fluoride (HF). The solid intermediate reaction products are conveyed to a second fluidized bed reactor at which the mol fraction of HF is controlled at low levels in order to prevent the formation of uranium tetrafluoride (UF 4 ). The first intermediate reaction products are reacted in the second fluidized bed with steam and hydrogen at a temperature of about 630 0 C. The second intermediate reaction product including uranium dioxide (UO 2 ) is conveyed to a third fluidized bed reactor and reacted with additional steam and hydrogen at a temperature of about 650 0 C producing a reaction product consisting essentially of uranium dioxide having an oxygen-uranium ratio of about 2 and a low residual fluoride content. This product is then conveyed to a fourth fluidized bed wherein a mixture of air and preheated nitrogen is introduced in order to further reduce the fluoride content of the UO 2 and increase the oxygen-uranium ratio to about 2.25

The mechanism of uranium adsorption on Resin 508 and isoelectric point of the resin

International Nuclear Information System (INIS)

Han Qingping; Lu Weichang; Su Huijuan; Hu Jinbo; Zhang Liqin; Chen Banglin

1990-01-01

The adsorption process of uranium by Resin 508 at the solid-liquid interface was investigated and the mechanism of uranium adsorption including adsorption dynamics, adsorption thermodynamics and isoelectric point of resin was studied. The results are as follows: The maximum of uranium adsorption is attained at pH5-7; Uranium adsorption isotherm by Resin 508 in experimental conditions agrees with Langmuir's adsorption isotherm, the maximum of uranium adsorbed (Vm) is 716 mg U/g-dried resin; The adsorption of uranium by Resin 508 is an endothermic reaction and ΔH = 16.87 kJ/mol; The exchange-adsorption rate is mainly controlled by liquid film diffusion; The isoelectric points of Resin 508 before and after uranium adsorption are found to be pH7.5 and pH5.7 respectively. It is a specific adsorption for uranium

Irradiation of TZM: Uranium dioxide fuel pin at 1700 K

Science.gov (United States)

Mcdonald, G. E.

1973-01-01

A fuel pin clad with TZM and containing solid pellets of uranium dioxide was fission heated in a static helium-cooled capsule at a maximum surface temperature of 1700 K for approximately 1000 hr and to a total burnup of 2.0 percent of the uranium-235. The results of the postirradiation examination indicated: (1) A transverse, intergranular failure of the fuel pin occurred when the fuel pin reached 2.0-percent burnup. This corresponds to 1330 kW-hr/cu cm, where the volume is the sum of the fuel, clad, and void volumes in the fuel region. (2) The maximum swelling of the fuel pin was less than 1.5 percent on the fuel-pin diameter. (3) There was no visible interaction between the TZM clad and the UO2. (4) Irradiation at 1700 K produced a course-grained structure, with an average grain diameter of 0.02 centimeter and with some of the grains extending one-half of the thickness of the clad. (5) Below approximately 1500 K, the irradiation of the clad produced a moderately fine-grained structure, with an average grain diameter of 0.004 centimeter.

Effect of small additions of silicon, iron, and aluminum on the room-temperature tensile properties of high-purity uranium

International Nuclear Information System (INIS)

Ludwig, R.L.

1983-01-01

Eleven binary and ternary alloys of uranium and very low concentrations of iron, silicon, and aluminum were prepared and tested for room-temperature tensile properties after various heat treatments. A yield strength approximately double that of high-purity derby uranium was obtained from a U-400 ppM Si-200 ppM Fe alloy after beta solution treatment and alpha aging. Higher silicon plus iron alloy contents resulted in increased yield strength, but showed an unacceptable loss of ductility

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

International Nuclear Information System (INIS)

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

1977-01-01

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

Adsorption of uranium from aqueous solution by PAMAM dendron functionalized styrene divinylbenzene

Energy Technology Data Exchange (ETDEWEB)

Ilaiyaraja, P., E-mail: chemila07@gmail.com [Radiological Safety Division, Radiological Safety and Environmental Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102, Tamilnadu (India); Singha Deb, Ashish Kumar; Sivasubramanian, K. [Radiological Safety Division, Radiological Safety and Environmental Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102, Tamilnadu (India); Ponraju, D. [Safety Engineering Division, Reactor Design Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102, Tamilnadu (India); Venkatraman, B. [Radiological Safety Division, Radiological Safety and Environmental Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102, Tamilnadu (India)

2013-04-15

Highlights: ► A new chelating resin PAMAMG{sub 3} -SDB has been synthesized for uranium adsorption. ► The maximum adsorption capacity was determined to be 130.25 mg g{sup −1} at pH 5.5. ► Adsorption capacity increases linearly with increasing dendron generation. ► The adsorbed uranium shall be easily desorbed by simply adjusting the pH < 3. ► Quantitative adsorption of uranium was observed even at high ionic strength. -- Abstract: A new polymeric chelating resin was prepared by growing third generation poly(amido)amine (PAMAMG{sub 3}) dendron on the surface of styrene divinylbenzene (SDB) and characterized by FTIR, TGA and SEM. The ideal branching of dendron in the chelating resin was determined from potentiometric titration. Adsorption of uranium (VI) from aqueous solution using PAMAMG{sub 3}-SDB chelating resin was studied in a series of batch experiments. Effect of contact time, pH, ionic strength, adsorbent dose, initial U(VI) concentration, dendron generation and temperature on adsorption of U(VI) were investigated. Kinetic experiments showed that U(VI) adsorption on PAMAMG{sub 3}-SDB followed pseudo-second-order kinetics model appropriately and equilibrium data agreed well with the Langmuir isotherm model. Thermodynamic parameters (ΔH°, ΔS°, ΔG°) were evaluated from temperature dependent adsorption data and the uranium adsorption on PAMAMG{sub 3}-SDB was found to be endothermic and spontaneous in nature. The sticking probability value (5.303 × 10{sup −9}), kinetic and isotherm data reveal the chemisorption of uranium on PAMAMG{sub 3}-SDB and adsorption capacity of the chelating resin was estimated to be 130.25 mg g{sup −1} at 298 K. About 99% of adsorbed U(VI) can be desorbed from PAMAMG{sub 3}-SDB by a simple acid treatment suggesting that the chelating resin is reusable.

Electrodeposition of uranium metal by reduction of uranium oxides in molten Lif-KF=NaF-CaF 2-UF4

International Nuclear Information System (INIS)

Pao, D.S.; Burris, L.; Steunenberg, R.K.; Tomczuk, Z.

1990-01-01

Although electrolytic reduction of uranium oxides was shown to be feasible in the early 1960's it is recognized that considerable improvement in the electrolytic reduction technology must be achieved for practical applications. This exploratory work on electrolytic reduction of uranium oxide was undertaken to investigate potential improvements in the technology. The approach taken was to deposit solid uranium metal directly on a solid cathode at temperatures below the melting point of uranium (1132 degrees C). The lower temperature electrolytic reduction process has several advantages over the existing chemical reduction processes. It lessens materials problems and special heating and insulating requirements associated with high-temperature operations. It removes most impurities. It does not produce the large quantities of byproduct oxides wastes typical of chemical reduction processes

Finding of no significant impact: Interim storage of enriched uranium above the maximum historical level at the Y-12 Plant Oak Ridge, Tennessee

International Nuclear Information System (INIS)

1995-01-01

The US Department of Energy (DOE) has prepared an Environmental Assessment (EA) for the Proposed Interim Storage of Enriched Uranium Above the Maximum Historical Storage Level at the Y-12 Plant, Oak Ridge, Tennessee (DOE/EA-0929, September, 1994). The EA evaluates the environmental effects of transportation, prestorage processing, and interim storage of bounding quantities of enriched uranium at the Y-12 Plant over a ten-year period. The State of Tennessee and the public participated in public meetings and workshops which were held after a predecisional draft EA was released in February 1994, and after the revised pre-approval EA was issued in September 1994. Comments provided by the State and public have been carefully considered by the Department. As a result of this public process, the Department has determined that the Y-12 Plant-would store no more than 500 metric tons of highly enriched uranium (HEU) and no more than 6 metric tons of low enriched uranium (LEU). The bounding storage quantities analyzed in the pre-approval EA are 500 metric tons of HEU and 7,105.9 metric tons of LEU. Based on-the analyses in the EA, as revised by the attachment to the Finding of No Significant Impact (FONSI), DOE has determined that interim storage of 500 metric tons of HEU and 6 metric tons of LEU at the Y-12 Plant does not constitute a major Federal action significantly affecting the quality of the human environment, within the meaning of the National Environmental Policy Act (NEPA) of 1969. Therefore, an Environmental Impact Statement (EIS) is not required and the Department is issuing this FONSI

Solid phase extraction of uranium(VI) onto benzoylthiourea-anchored activated carbon

Energy Technology Data Exchange (ETDEWEB)

Zhao Yongsheng; Liu Chunxia; Feng Miao; Chen Zhen; Li Shuqiong; Tian Gan; Wang Li; Huang Jingbo [College of Chemistry, Sichuan University, 29 Wangjiang Lu, Chengdu, 610064, Sichuan (China); Li Shoujian, E-mail: sjli000616@scu.edu.cn [College of Chemistry, Sichuan University, 29 Wangjiang Lu, Chengdu, 610064, Sichuan (China)

2010-04-15

A new solid phase extractant selective for uranium(VI) based on benzoylthiourea anchored to activated carbon was developed via hydroxylation, amidation and reaction with benzoyl isothiocyanate in sequence. Fourier transform infrared spectroscopy and total element analysis proved that benzoylthiourea had been successfully grafted to the surface of the activated carbon, with a loading capacity of 1.2 mmol benzoylthiourea per gram of activated carbon. The parameters that affect the uranium(VI) sorption, such as contact time, solution pH, initial uranium(VI) concentration, adsorbent dose and temperature, have been investigated. Results have been analyzed by Langmuir and Freundlich isotherm; the former was more suitable to describe the sorption process. The maximum sorption capacity (82 mg/g) for uranium(VI) was obtained at experimental conditions. The rate constant for the uranium sorption by the as-synthesized extractant was 0.441 min{sup -1} from the first order rate equation. Thermodynamic parameters ({Delta}H{sup 0} = -46.2 kJ/mol; {Delta}S{sup 0} = -98.0 J/mol K; {Delta}G{sup 0} = -17.5 kJ/mol) showed the adsorption of an exothermic process and spontaneous nature, respectively. Additional studies indicated that the benzoylthiourea-anchored activated carbon (BT-AC) selectively sorbed uranyl ions in the presence of competing ions, Na{sup +}, Co{sup 2+}, Sr{sup 2+}, Cs{sup +} and La{sup 3+}.

A Hybrid Maximum Power Point Search Method Using Temperature Measurements in Partial Shading Conditions

Directory of Open Access Journals (Sweden)

Mroczka Janusz

2014-12-01

Full Text Available Photovoltaic panels have a non-linear current-voltage characteristics to produce the maximum power at only one point called the maximum power point. In the case of the uniform illumination a single solar panel shows only one maximum power, which is also the global maximum power point. In the case an irregularly illuminated photovoltaic panel many local maxima on the power-voltage curve can be observed and only one of them is the global maximum. The proposed algorithm detects whether a solar panel is in the uniform insolation conditions. Then an appropriate strategy of tracking the maximum power point is taken using a decision algorithm. The proposed method is simulated in the environment created by the authors, which allows to stimulate photovoltaic panels in real conditions of lighting, temperature and shading.

Study of elementary mechanisms of creep in uranium as a function of temperature (150 deg. to 760 deg. C) by activation energy measurements; Etude des mecanismes elementaires de deformation par fluage de l'uranium en fonction de la temperature (de 150 deg. a 760 deg. C) par la mesure des energies d'activation

Energy Technology Data Exchange (ETDEWEB)

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

1967-07-01

Creep tests were carried out on single crystals and polycrystalline specimens of uranium in both the {alpha} and {beta} phases over the temperature range 150 - 760 deg. C. The determination of the activation energy for creep and the study of its variation with temperature made it possible to distinguish various temperature ranges in which one or more elementary mechanisms govern deformation. Micrographic observations after creep and the study of the variation of creep-rate with load support the conclusions. The creep behavior of single crystals is identical with that of polycrystalline material below 325 deg. C. From 325 deg. C to one upper limiting temperature whose value depends on the purity and previous history of the metal, the creep deformation of uranium is controlled by cross-slip. From this limiting temperature up to 520 deg. C, the creep of uranium involves two independent mechanisms operating simultaneously, the movement of screw dislocation by cross-slip and the climbing of edge dislocations out of their slip plane. Between 520 deg. C and the {alpha} - {beta} transformation temperature creep in polycrystals is governed by the climb of edge dislocations out of their slip planes, by a pile up mechanism in the case of primary creep and by dipole annihilation in the case of secondary creep. In single crystals creep is dependent on the climb of edge dislocations into pre-existent sub-boundaries and their subsequent rearrangement within these boundaries. In the {beta} phase the creep of polycrystals is governed by the diffusional climb of edge dislocations. Between 450 and 630 deg. C small alloy additions of molybdenum modify the creep characteristics of uranium although the deformation mechanisms involved are analogous to those in the pure metal. (author) [French] Des essais de fluage a diverses temperatures comprises entre 150 et 760 deg. C ont ete effectues sur des polycristaux et des monocristaux d'uranium, en phase {alpha} et en phase {beta}. La

Process for preparing sintered uranium dioxide nuclear fuel

International Nuclear Information System (INIS)

Carter, R.E.

1975-01-01

Uranium dioxide is prepared for use as fuel in nuclear reactors by sintering it to the desired density at a temperature less than 1300 0 C in a chemically controlled gas atmosphere comprised of at least two gases which in equilibrium provide an oxygen partial pressure sufficient to maintain the uranium dioxide composition at an oxygen/uranium ratio of at least 2.005 at the sintering temperature. 7 Claims, No Drawings

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.

Uranium Dioxide Powder Flow ability Improvement Using Sol-Gel

International Nuclear Information System (INIS)

Juanda, D.; Sambodo Daru, G.

1998-01-01

The improvement of flow ability characteristics of uranium dioxide powder has been done using sol-gel process. To anticipate a pellet mass production with uniform pellet dimension, the uranium dioxide powder must be have a spherical form. Uranium dioxide spherical powder has been diluted in acid transformed into sol colloidal solution. To obtain uranium dioxide spherical form, the uranium sol-colloidal solution has been dropped in a hot paraffin ( at the temperature of 90 0 C) to form gelatinous colloid and then dried at 800 0 C, and sintered at the temperature of 1700 0 C. The flow ability of spherical uranium dioxide powder has been examined by using Flowmeter Hall (ASTM. B. 213-46T). The measurement result reveals that the spherical uranium dioxide powder has a flow ability twice than that of unprocessed uranium dioxide powder

Trends in Mean Annual Minimum and Maximum Near Surface Temperature in Nairobi City, Kenya

Directory of Open Access Journals (Sweden)

George Lukoye Makokha

2010-01-01

Full Text Available This paper examines the long-term urban modification of mean annual conditions of near surface temperature in Nairobi City. Data from four weather stations situated in Nairobi were collected from the Kenya Meteorological Department for the period from 1966 to 1999 inclusive. The data included mean annual maximum and minimum temperatures, and was first subjected to homogeneity test before analysis. Both linear regression and Mann-Kendall rank test were used to discern the mean annual trends. Results show that the change of temperature over the thirty-four years study period is higher for minimum temperature than maximum temperature. The warming trends began earlier and are more significant at the urban stations than is the case at the sub-urban stations, an indication of the spread of urbanisation from the built-up Central Business District (CBD to the suburbs. The established significant warming trends in minimum temperature, which are likely to reach higher proportions in future, pose serious challenges on climate and urban planning of the city. In particular the effect of increased minimum temperature on human physiological comfort, building and urban design, wind circulation and air pollution needs to be incorporated in future urban planning programmes of the city.

Drawing of uranium in {gamma} phase; Filage de l'uranium en phase gamma

Energy Technology Data Exchange (ETDEWEB)

Stohr, J.A. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires; Chevigny, R. [Conpagnie, Pechiney, 73 - Chambery (France)

1955-07-01

It describes the study of working and drawing of uranium in {gamma} phase. In a first part, the forgeable characteristics of uranium metal in the three different phases ({alpha}, {beta} and {gamma}) are compared by using BASTIEN-PORTEVIN method. The different experiments are testing the behaviour metal in each phase under different stresses and a temperature gradient as slow and shock traction, slow and shock compression, resilience, flexibility. Results show that optimum conditions for uranium drawing is uranium in phase {gamma}. In a second part, it described the drawing method and process. The uranium rods obtained by this technique are of very good quality. In addition, the material wear is very low which permits a low production cost. Finally, the uranium rod physical properties are studied. (M.P.)

Long-term ecological effects of exposure to uranium

International Nuclear Information System (INIS)

Hanson, W.C.; Miera, F.R. Jr.

1976-03-01

The consequences of releasing natural and depleted uranium to terrestrial ecosystems during development and testing of depleted uranium munitions were investigated. At Eglin Air Force Base, Florida, soil at various distances from armor plate target butts struck by depleted uranium penetrators was sampled. The upper 5 cm of soil at the target bases contained an average of 800 ppM of depleted uranium, about 30 times as much as soil at 5- to 10-cm depth, indicating some vertical movement of depleted uranium. Samples collected beyond about 20 m from the targets showed near-background natural uranium levels, about 1.3 +- 0.3 μg/g or ppM. Two explosives-testing areas at the Los Alamos Scientific Laboratory (LASL) were selected because of their use history. E-F Site soil averaged 2400 ppM of uranium in the upper 5 cm and 1600 ppM at 5-10 cm. Lower Slobovia Site soil from two subplots averaged about 2.5 and 0.6 percent of the E-F Site concentrations. Important uranium concentration differences with depth and distance from detonation points were ascribed to the different explosive tests conducted in each area. E-F Site vegetation samples contained about 320 ppM of uranium in November 1974 and about 125 ppM in June 1975. Small mammals trapped in the study areas in November contained a maximum of 210 ppM of uranium in the gastrointestinal tract contents, 24 ppM in the pelt, and 4 ppM in the remaining carcass. In June, maximum concentrations were 110, 50, and 2 ppM in similar samples and 6 ppM in lungs. These data emphasized the importance of resuspension of respirable particles in the upper few millimeters of soil as a contamination mechanism for several components of the LASL ecosystem

Some characteristics of uranium oxides in China

International Nuclear Information System (INIS)

Xu, Guoqing; Wang, Aizhen; Gu, Qifang; Zhang, Jingyi; Zhang, Zhaoming; Huang, Yuzhu

1981-01-01

According to the analytical data of seventy-seven samples from several tens of uranium ore deposits and occurrences in China, chemical properties, cell dimensions and reflectance of uranium oxides are studied. Chemical properties of uranium oxides from different types of uranium ore deposits and the influence of various mineralization ages and hosts on the compositions of uranium oxides are presented. The influence of these factor such as mineralization temperatures, the compositions of hosts and geochemical background on the compositions of uranium oxides are evident. Lead in proterozoic uranium oxides is relatively enriched by the decay of radio-active elements. Cell dimensions have positive correlation with mineralization ages, formation temperatures and concentration of rare earths and Pb, and negative correlation with the oxidation coefficient. The cell size is an exponential function of the content in CaO. It is suggested that among the factors of influence the most important is the mineralization temperature. The size of ionic radius of elements substituted U 4 + and autooxidation of U 4 + during the process of the decay of radioactive elements are of secondary importance. The reflectance is independent of the content of CaO and SiO 2 . The reflectance is positively correlative with the cell size and negatively correlative with oxidation coefficient. The relation between the reflectance and the content of PbO is logarithmic

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

Energy Technology Data Exchange (ETDEWEB)

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

1965-07-01

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

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)

Activity concentration of uranium in groundwater from uranium mineralized areas and its neighborhood

International Nuclear Information System (INIS)

Arabi, S.A.; Funtua, I.I.; Dewu, B.B.M.; Alagbe, S.A.; Garba, M.L.; Kwaya, M.Y.; Baloga, A.D.

2013-01-01

Uranium mineralization in parts of northeastern Nigeria necessitated its exploration during early eighties by the Nigeria Uranium Mining Company (NUMCO) which was later abandoned. During their course of decay, uranium isotopes pass through radioactive decay stage and eventually into stable isotope of lead. The course of concern for soluble uranium in groundwater especially from the mineralized areas include ionizing radiation, chemical toxicity and reproductive defects for which ingested uranium has been implicated to have caused. This study is aimed at assessing the levels of concentration of uranium in groundwater to ascertain its compliance with the World Health Organization's (WHO) and the United State Environmental Protection Agency's (EPA) guideline for uranium in drinking water. Thirty five groundwater samples were collected using EPA's groundwater sampling protocol and analyzed at the Department of Geology, University of Cape Town using an Inductively Coupled Plasma Mass Spectrometric (ICP-MS) technique. Significant finding of this work was that there is radiological contamination of groundwater in the area. There is also an indication that the extent of radiological contamination is not much within the mineralized zones, therefore, there is likelihood that groundwater has acted as a medium of transporting and enhancing uranium in groundwater in an environment away from that of origin. About 5.7 % of the samples studied had uranium concentration above WHO and EPA's maximum contaminant level of 30 μg/L which is a major concern for inhabitants of the area. It was also apparent that radiological contamination at the southwestern part of the study area extends into the adjacent sheet (sheet 152). Uranium concentration above set standards in those areas might have originated from rocks around established mineralized zones but was transported to those contaminated areas by groundwater that leaches across the host rock and subsequently mobilizing soluble uranium

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

Directory of Open Access Journals (Sweden)

Fawwaz I. Khalili

2013-01-01

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

METHOD OF APPLYING NICKEL COATINGS ON URANIUM

Science.gov (United States)

Gray, A.G.

1959-07-14

A method is presented for protectively coating uranium which comprises etching the uranium in an aqueous etching solution containing chloride ions, electroplating a coating of nickel on the etched uranium and heating the nickel plated uranium by immersion thereof in a molten bath composed of a material selected from the group consisting of sodium chloride, potassium chloride, lithium chloride, and mixtures thereof, maintained at a temperature of between 700 and 800 deg C, for a time sufficient to alloy the nickel and uranium and form an integral protective coating of corrosion-resistant uranium-nickel alloy.

Temperature dependence of attitude sensor coalignments on the Solar Maximum Mission (SMM)

Science.gov (United States)

Pitone, D. S.; Eudell, A. H.; Patt, F. S.

1990-01-01

The temperature correlation of the relative coalignment between the fine-pointing sun sensor and fixed-head star trackers measured on the Solar Maximum Mission (SMM) is analyzed. An overview of the SMM, including mission history and configuration, is given. Possible causes of the misalignment variation are discussed, with focus placed on spacecraft bending due to solar-radiation pressure, electronic or mechanical changes in the sensors, uncertainty in the attitude solutions, and mounting-plate expansion and contraction due to thermal effects. Yaw misalignment variation from the temperature profile is assessed, and suggestions for spacecraft operations are presented, involving methods to incorporate flight measurements of the temperature-versus-alignment function and its variance in operational procedures and the spacecraft structure temperatures in the attitude telemetry record.

Pyrophoricity of uranium in long-term storage environments

International Nuclear Information System (INIS)

Solbrig, C.W.; Krsul, J.R.; Olsen, D.N.

1994-01-01

A corrosion cycle for uranium is postulated which can be used to assess whether a given storage situation might produce fire hazards and/or continual uranium corrosion. A significant reaction rate of uranium and moisture occurs at room temperature which produces uranium oxide and hydrogen. If the hydrogen cannot escape, it will react slowly with uranium to form uranium hydride. The hydride is pyrophoric at room temperature when exposed to air. Either the hydrogen or the hydride can produce a dangerous situation as demonstrated by two different incidents described here. Long-term corrosion will occur even if the normal precautions are taken as is demonstrated by the long-term storage of stainless steel clad uranium fuel plates. The major initiator of these problems is attributed to any moisture condensed on the metal or any brought in by the cover gas. The postulated corrosion cycle is used to suggest ways to circumvent these problems

Dissolution experiments of unirradiated uranium dioxide pellets

International Nuclear Information System (INIS)

Ollila, K.

1985-01-01

The purpose of this study was to measure the dissolution rate of uranium from unirradiated uranium dioxide pellets in deionized water and natural groundwater. Moreover, the solubility limit of uranium in natural groundwater was measured. Two different temperatures, 25 and 60 deg C were used. The low oxygen content of deep groundwater was simulated. The dissolution rate of uranium varied from 10 -7 to 10 -8 g cm -2 d -1 . The rate in reionized water was one order of magnitude lower than in groundwater. No great difference was observed between the natural groundwaters with different composition. Temperature seems to have effect on the dissolution rate. The solubility limit of uranium in natural groundwater in reducing conditions, at 25 deg C, varied from 20 to 600 μg/l and in oxidizing conditions, at 60 deg C, from 4 to 17 mg/l

Study of elementary mechanisms of creep in uranium as a function of temperature (150 deg. to 760 deg. C) by activation energy measurements

International Nuclear Information System (INIS)

Grenier, P.

1966-06-01

Creep tests were carried out on single crystals and polycrystalline specimens of uranium in both the α and β phases over the temperature range 150 - 760 deg. C. The determination of the activation energy for creep and the study of its variation with temperature made it possible to distinguish various temperature ranges in which one or more elementary mechanisms govern deformation. Micrographic observations after creep and the study of the variation of creep-rate with load support the conclusions. The creep behavior of single crystals is identical with that of polycrystalline material below 325 deg. C. From 325 deg. C to one upper limiting temperature whose value depends on the purity and previous history of the metal, the creep deformation of uranium is controlled by cross-slip. From this limiting temperature up to 520 deg. C, the creep of uranium involves two independent mechanisms operating simultaneously, the movement of screw dislocation by cross-slip and the climbing of edge dislocations out of their slip plane. Between 520 deg. C and the α - β transformation temperature creep in polycrystals is governed by the climb of edge dislocations out of their slip planes, by a pile up mechanism in the case of primary creep and by dipole annihilation in the case of secondary creep. In single crystals creep is dependent on the climb of edge dislocations into pre-existent sub-boundaries and their subsequent rearrangement within these boundaries. In the β phase the creep of polycrystals is governed by the diffusional climb of edge dislocations. Between 450 and 630 deg. C small alloy additions of molybdenum modify the creep characteristics of uranium although the deformation mechanisms involved are analogous to those in the pure metal. (author) [fr

Method for preparation of uranium hydride

International Nuclear Information System (INIS)

Gorski, M.S.; Goncalves, Miriam; Mirage, A.; Lima, W. de.

1985-01-01

A method for preparation of Uranium Hydride starting from Hidrogen and Uranium is described. In the temperature range of 250 0 up to 350 0 C, and pressures above 10torr, Hydrogen reacts smoothly with Uranium turnings forming a fine black or dark gray powder (UH 3 ). Samples containing a significant amount of oxides show a delay before the reaction begging. (Author) [pt

Uranium loss from BISO-coated weak-acid-resin HTGR fuel

International Nuclear Information System (INIS)

Pearson, R.L.; Lindemer, T.B.

1977-02-01

Recycle fuel for the High-Temperature Gas-Cooled Reactor (HTGR) contains a weak-acid-resin (WAR) kernel, which consists of a mixture of UC 2 , UO 2 , and free carbon. At 1900 0 C, BISO-coated WAR UC 2 or UC 2 -UO 2 kernels lose a significant portion of their uranium in several hundred hours. The UC 2 decomposes and uranium diffuses through the pyrolytic coating. The rate of escape of the uranium is dependent on the temperature and the surface area of the UC 2 , but not on a temperature gradient. The apparent activation energy for uranium loss, ΔH, is approximately 90 kcal/mole. Calculations indicate that uranium loss from the kernel would be insignificant under conditions to be expected in an HTGR

REMOVAL OF URANIUM FROM DRINKING WATER BY CONVENTIONAL TREATMENT METHODS

Science.gov (United States)

The USEPA currently does not regulate uranium in drinking water but will be revising the radionuclide regulations during 1989 and will propose a maximum contaminant level for uranium. The paper presents treatment technology information on the effectiveness of conventional method...

Novel precipitation technique for uranium recovery from carbonate leach solutions

International Nuclear Information System (INIS)

Sujoy Biswas; Rupawate, V.H.; Hareendran, K.N.; Roy, S.B.; Chakravartty, J.K.

2015-01-01

The recovery of uranium from carbonate ore leach solution was studied using novel precipitation method. The uranium from leach liquor was recovered as magnesium diuranate with NaOH in presence of trace amount of Mg 2+ . Effects of various parameters such as addition of H 2 SO 4 , MgO, MgSO 4 as well as NaOH were investigated for maximum uranium recovery. Overall uranium recovery of the process was 97 % with improved particle size (∼57 µm). Based on the experimental findings, a process flow-sheet was developed for uranium recovery from carbonate ore leach solution with a uranium concentration of <1 g/L. (author)

Internal friction in uranium dioxide

International Nuclear Information System (INIS)

Paulin Filho, Pedro Iris

1979-01-01

The uranium dioxide inelastic properties were studied measuring internal friction at low frequencies (of the order of 1 Hz). The work was developed in the 160 to 400 deg C temperature range. The effect of stoichiometry variation was studied oxidizing the sample with consequent change of the defect structure originally present in the non-stoichiometric uranium dioxide. The presence of a wide and irregular peak due to oxidation was observed at low temperatures. Activation energy calculations indicated the occurrence of various relaxation processes and assuming the existence of a peak between - 80 and - 70 deg C , the absolute value obtained for the activation energy (0,54 eV) is consistent with the observed values determined at medium and high frequencies for the stress induced reorientation of defects. The microstructure effect on the inelastic properties was studied for stoichiometric uranium dioxide, by varying grain size and porosity. These parameters have influence on the high temperature measurements of internal friction. The internal friction variation for temperatures higher than 340 deg C is thought to be due to grain boundary relaxation phenomena. (author)

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

Science.gov (United States)

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

1959-02-24

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

Analytical and numerical models of uranium ignition assisted by hydride formation

International Nuclear Information System (INIS)

Totemeier, T.C.; Hayes, S.L.

1996-01-01

Analytical and numerical models of uranium ignition assisted by the oxidation of uranium hydride are described. The models were developed to demonstrate that ignition of large uranium ingots could not occur as a result of possible hydride formation during storage. The thermodynamics-based analytical model predicted an overall 17 C temperature rise of the ingot due to hydride oxidation upon opening of the storage can in air. The numerical model predicted locally higher temperature increases at the surface; the transient temperature increase quickly dissipated. The numerical model was further used to determine conditions for which hydride oxidation does lead to ignition of uranium metal. Room temperature ignition only occurs for high hydride fractions in the nominally oxide reaction product and high specific surface areas of the uranium metal

Solvent extraction of uranium from high acid leach solution

International Nuclear Information System (INIS)

Ramadevi, G.; Sreenivas, T.; Navale, A.S.; Padmanabhan, N.P.H.

2010-01-01

A significant part of the total uranium reserves all over the world is contributed by refractory uranium minerals. The refractory oxides are highly stable and inert to attack by most of the commonly used acids under normal conditions of acid strength, pressure and temperature. Quantitative dissolution of uranium from such ores containing refractory uranium minerals requires drastic operating conditions during chemical leaching like high acid strength, elevated pressures and temperatures. The leach liquors produced under these conditions normally have high free acidity, which affects the downstream operations like ion exchange and solvent extraction

Uranium in Kosovo's drinking water.

Science.gov (United States)

Berisha, Fatlume; Goessler, Walter

2013-11-01

The results of this paper are an initiation to capture the drinking water and/or groundwater elemental situation in the youngest European country, Kosovo. We aim to present a clear picture of the natural uranium concentration in drinking water and/or groundwater as it is distributed to the population of Kosovo. Nine hundred and fifty-one (951) drinking water samples were analyzed by inductively coupled plasma mass spectrometry (ICPMS). The results are the first countrywide interpretation of the uranium concentration in drinking water and/or groundwater, directly following the Kosovo war of 1999. More than 98% of the samples had uranium concentrations above 0.01 μg L(-1), which was also our limit of quantification. Concentrations up to 166 μg L(-1) were found with a mean of 5 μg L(-1) and median 1.6 μg L(-1) were found. Two point six percent (2.6%) of the analyzed samples exceeded the World Health Organization maximum acceptable concentration of 30 μg L(-1), and 44.2% of the samples exceeded the 2 μg L(-1) German maximum acceptable concentrations recommended for infant food preparations. Copyright © 2013 Elsevier Ltd. All rights reserved.

A melt refining method for uranium-contaminated aluminum

International Nuclear Information System (INIS)

Uda, T.; Iba, H.; Hanawa, K.

1986-01-01

Melt refining of uranium-contaminated aluminum which has been difficult to decontaminate because of the high reactivity of aluminum, was experimentally studied. Samples of contaminated aluminum and its alloys were melted after adding various halide fluxes at various melting temperatures and various melting times. Uranium concentration in the resulting ingots was determined. Effective flux compositions were mixtures of chlorides and fluorides, such as LiF, KCl, and BaCl 2 , at a fluoride/chloride mole ratio of 1 to 1.5. The removal of uranium from aluminum (the ''decontamination effect'') increased with decreasing melting temperature, but the time allowed for reaction had little influence. Pure aluminum was difficult to decontaminate from uranium; however, uranium could be removed from alloys containing magnesium. This was because the activity of the aluminum was decreased by formation of the intermetallic compound Al-Mg. With a flux of LiF-KCl-BaCl 2 and a temperature of 800 0 C, uranium added to give an initial concentration of 500 ppm was removed from a commercial alloy of aluminum, A5056, which contains 5% magnesium, to a final concentration of 0.6 ppm, which is near that in the initial aluminum alloy

Corium Oxidation at Temperatures Above 2000 K

International Nuclear Information System (INIS)

Hagrman, Donald L.; Rempe, Joy L.

2001-01-01

A mechanistic model, based on a quasi-equilibrium analysis of oxidation reactions, is proposed for predicting high-temperature corium oxidation. The analysis suggests that oxide forming on the surface of corium containing uranium, zirconium, and iron is similar to the oxides formed on zirconium and uranium as long as there is a small percentage of unoxidized zirconium or uranium in the metallic phase. This is because of the higher affinity of zirconium and uranium for oxygen. Hence, oxidation rates and heat production rates are similar to (U,Zr) compounds until nearly all the uranium and zirconium in the corium oxidizes. Oxidation rates after this point are predicted to be similar to those implied by the oxide thickness present when the forming oxide ceases to be protective, and heat generation rates should be similar to those implied by iron oxidation, i.e., ∼4% of the zirconium oxidation heating rate.The maximum atomic ratio of unoxidized iron to unoxidized liquid zirconium plus uranium for the formation of a solid protective oxide below 2800 K is estimated for a temperature, T (in Kelvin), as follows:(unoxidized iron)/(unoxidized zirconium + turanium) = (1/28){5.7/exp[-(147 061 + 12.08T log(T) - 61.03T - 0.000555T 2 /1.986T)]} 1/2 .As long as this limit is not exceeded, either zirconium or uranium metal oxidation rates and heating describe the corium oxidation rate. If this limit is exceeded, diffusion of steam to the corium surface will limit the oxidation rate, and linear time-dependent growth of a nonprotective, mostly FeO, layer will occur below the protective (Zr,U) O 2 scale. When this happens, the oxidation should be at the constant rate given by the thickness of the protective layer. Heat generation should be similar to that of iron oxidation

Corium Oxidation at Temperatures Above 2000 K

Energy Technology Data Exchange (ETDEWEB)

Hagrman, Donald Lee; Rempe, Joy Lynn

2001-02-01

A mechanistic model, based on a quasi-equilibrium analysis of oxidation reactions, is proposed for predicting high-temperature corium oxidation. The analysis suggests that oxide forming on the surface of corium containing uranium, zirconium, and iron is similar to the oxides formed on zirconium and uranium as long as there is a small percentage of unoxidized zirconium or uranium in the metallic phase. This is because of the higher affinity of zirconium and uranium for oxygen. Hence, oxidation rates and heat production rates are similar to (U,Zr) compounds until nearly all the uranium and zirconium in the corium oxidizes. Oxidation rates after this point are predicted to be similar to those implied by the oxide thickness present when the forming oxide ceases to be protective, and heat generation rates should be similar to those implied by iron oxidation, i.e., ~4% of the zirconium oxidation heating rate. The maximum atomic ratio of unoxidized iron to unoxidized liquid zirconium plus uranium for the formation of a solid protective oxide below 2800 K is estimated for a temperature, T (in Kelvin), as follows: (unoxidized iron)/(unoxidized zirconium + turanium) = (1/28){5.7/exp[-(147 061 + 12.08T log(T) - 61.03T - 0.000555T2/1.986T)]}1/2. As long as this limit is not exceeded, either zirconium or uranium metal oxidation rates and heating describe the corium oxidation rate. If this limit is exceeded, diffusion of steam to the corium surface will limit the oxidation rate, and linear time-dependent growth of a nonprotective, mostly FeO, layer will occur below the protective (Zr,U) O2 scale. When this happens, the oxidation should be at the constant rate given by the thickness of the protective layer. Heat generation should be similar to that of iron oxidation.

Sorption of uranium by cellulose derivatives

International Nuclear Information System (INIS)

Muroi, M.; Imai, S.; Hamaguchi, A.

1985-01-01

The sorption behaviour of uranium was investigated by batch and column methods using four cellulose derivatives, two having an amino group and two having an amino group plus a dithiocarboxylate group. All four derivatives showed maximum uranium sorption from pure water in the neutral region or from artificial sea water in the acidic region. In the batch method, quantitative removal of 100 μg of uranium from 50 ml of water at pH 5.0 was achieved by equilibration with 50 mg of any of the four sorbents. The percentage removal under these conditions decreased gradually with increasing concentration of uranium above 100 μg per 50 ml. A similar high percentage removal of uranium was achieved using artificial sea water. In the column method, quantitative removal of 5 μg of uranium from 1l of water at pH 6.7 was achieved with 200 mg of either of the two sorbents. Similar quantitative removal of uranium was achieved from 1l of artificial sea water at pH 5.4 with 500 mg of either of the two sorbents. (author)

Behaviour of uranium under irradiation; Comportement de l'uranium sous irradiation

Energy Technology Data Exchange (ETDEWEB)

Adda, Y; Mustelier, J P; Quere, Y [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires; Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

1964-07-01

The main results obtained in a study of the formation of defects caused in uranium by fission at low temperature are reported. By irradiation at 20 K. it was possible to determine the number of Frenkel pairs produced by one fission. An analysis of the curves giving the variations in electrical resistivity shows the size of the displacement spikes and the mechanism of defect creation due to fission. Irradiations at 77 K gave additional information, showing behaviour differences in the case of recrystallised and of cold worked uranium. The diffusion of rare gases was studied using metal-rare gas alloys obtained by electrical discharge, and samples of irradiated uranium. Simple diffusion is only responsible for the release of the rare gases under vacuum in cases where the rare gas content is very low (very slightly irradiated U). On the other hand when the concentration is higher (samples prepared by electrical discharge) the gas is given off by the formation, growth and coalescence of bubbles; the apparent diffusion coefficient is then quite different from the true coefficient and cannot be used in calculations on swelling. The various factors governing the phenomenon of simple diffusion were examined. It was shown in particular that a small addition of molybdenum could reduce the diffusion coefficient by a factor of 100. The precipitation of gas in uranium (Kr), in silver (Kr) and in Al-Li alloy (He) have been followed by measurement of the crystal parameter and of the electrical resistivity, and by electron microscope examination of thin films. The important part played by dislocations in the generation and growth of bubbles has been demonstrated, and it has been shown also that precipitation of bubbles on the dislocation lattice could block the development of recrystallisation. The results of these studies were compared with observations made on the swelling of uranium and uranium alloys U Mo and U Nb strongly irradiated between 400 and 700 C. In the case of Cubic

Probabilistic measures of climate change vulnerability, adaptation action benefits, and related uncertainty from maximum temperature metric selection

Science.gov (United States)

DeWeber, Jefferson T.; Wagner, Tyler

2018-01-01

Predictions of the projected changes in species distributions and potential adaptation action benefits can help guide conservation actions. There is substantial uncertainty in projecting species distributions into an unknown future, however, which can undermine confidence in predictions or misdirect conservation actions if not properly considered. Recent studies have shown that the selection of alternative climate metrics describing very different climatic aspects (e.g., mean air temperature vs. mean precipitation) can be a substantial source of projection uncertainty. It is unclear, however, how much projection uncertainty might stem from selecting among highly correlated, ecologically similar climate metrics (e.g., maximum temperature in July, maximum 30‐day temperature) describing the same climatic aspect (e.g., maximum temperatures) known to limit a species’ distribution. It is also unclear how projection uncertainty might propagate into predictions of the potential benefits of adaptation actions that might lessen climate change effects. We provide probabilistic measures of climate change vulnerability, adaptation action benefits, and related uncertainty stemming from the selection of four maximum temperature metrics for brook trout (Salvelinus fontinalis), a cold‐water salmonid of conservation concern in the eastern United States. Projected losses in suitable stream length varied by as much as 20% among alternative maximum temperature metrics for mid‐century climate projections, which was similar to variation among three climate models. Similarly, the regional average predicted increase in brook trout occurrence probability under an adaptation action scenario of full riparian forest restoration varied by as much as .2 among metrics. Our use of Bayesian inference provides probabilistic measures of vulnerability and adaptation action benefits for individual stream reaches that properly address statistical uncertainty and can help guide conservation

Probabilistic measures of climate change vulnerability, adaptation action benefits, and related uncertainty from maximum temperature metric selection.

Science.gov (United States)

DeWeber, Jefferson T; Wagner, Tyler

2018-06-01

Predictions of the projected changes in species distributions and potential adaptation action benefits can help guide conservation actions. There is substantial uncertainty in projecting species distributions into an unknown future, however, which can undermine confidence in predictions or misdirect conservation actions if not properly considered. Recent studies have shown that the selection of alternative climate metrics describing very different climatic aspects (e.g., mean air temperature vs. mean precipitation) can be a substantial source of projection uncertainty. It is unclear, however, how much projection uncertainty might stem from selecting among highly correlated, ecologically similar climate metrics (e.g., maximum temperature in July, maximum 30-day temperature) describing the same climatic aspect (e.g., maximum temperatures) known to limit a species' distribution. It is also unclear how projection uncertainty might propagate into predictions of the potential benefits of adaptation actions that might lessen climate change effects. We provide probabilistic measures of climate change vulnerability, adaptation action benefits, and related uncertainty stemming from the selection of four maximum temperature metrics for brook trout (Salvelinus fontinalis), a cold-water salmonid of conservation concern in the eastern United States. Projected losses in suitable stream length varied by as much as 20% among alternative maximum temperature metrics for mid-century climate projections, which was similar to variation among three climate models. Similarly, the regional average predicted increase in brook trout occurrence probability under an adaptation action scenario of full riparian forest restoration varied by as much as .2 among metrics. Our use of Bayesian inference provides probabilistic measures of vulnerability and adaptation action benefits for individual stream reaches that properly address statistical uncertainty and can help guide conservation actions. Our

FORMING TUBES AND RODS OF URANIUM METAL BY EXTRUSION

Science.gov (United States)

Creutz, E.C.

1959-01-27

A method and apparatus are presented for the extrusion of uranium metal. Since uranium is very brittle if worked in the beta phase, it is desirable to extrude it in the gamma phase. However, in the gamma temperature range thc uranium will alloy with the metal of the extrusion dic, and is readily oxidized to a great degree. According to this patent, uranium extrusion in thc ganmma phase may be safely carried out by preheating a billet of uranium in an inert atmosphere to a trmperature between 780 C and 1100 C. The heated billet is then placed in an extrusion apparatus having dies which have been maintained at an elevated temperature for a sufficient length of time to produce an oxide film, and placing a copper disc between the uranium billet and the die.

The life of some metallic uranium based fuel elements; Duree de vie de quelques combustibles a base d'uranium metal

Energy Technology Data Exchange (ETDEWEB)

Stohr, J A; Englander, M [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1958-07-01

Description of some theoretical and experimental data concerning the design and most economic preparation of metallic uranium based fuel elements, which are intended to produce an energy of 3 kW days/g of uranium in a thermal reactor, at a sufficiently high mean temperature. Experimental results obtained by testing by analogy or by actually trying out fuel elements obtained by alloying uranium with other metals in proportions such that the resistance to deformation of the alloy produced is much higher than that of pure metallic uranium and that the thermal utilisation factor is only slightly different from that of the uranium. (author) [French] Description de quelques donnees theoriques et experimentales concernant la conception et la preparation la plus economique d'elements combustibles a base d'uranium metallique naturel, destines a degager dans un reacteur thermique une energie de l'ordre de 3 kWj/g d'uranium a une temperature moyenne suffisamment elevee. Resultats experimentaux acquis par tests analogiques ou reels sur combustibles obtenus par alliage de l'uranium avec des elements metalliques en proportions telles que la resistance a la deformation soit bien superieure a celle de l'uranium metal pur et que le facteur propre d'utilisation thermique n ne soit que peu affecte. (auteur)

Study of the Formation of Eutectic Melt of Uranium and Thermal Analysis for the Salt Distillation of Uranium Deposits

International Nuclear Information System (INIS)

Park, Sung Bin; Hwang, Sung Chan; Kang, Young Ho; Park, Ki Min; Jun, Wan Gi; Lee, Han Soo; Cho, Dong Wook

2010-01-01

Uranium deposits from an electrorefining process contain about 30% salt. In order to recover pure uranium and transform it into an ingot, the salts have to be removed from the uranium deposits. Major process variables for the salt distillation process of the uranium deposits are hold temperature and vacuum pressure. Effects of the variables on the salt removal efficiency were studied in the previous study 1. By applying the Hertz-Langmuir relation to the salt evaporation of the uranium deposits, the evaporation coefficients were obtained at the various conditions. The operational conditions for achieving above 99% salt removal were deduced. The salt distilled uranium deposits tend to form the eutectic melt with iron, nickel, chromium for structural material of salt evaporator. In this study, we investigated the hold temperature limitation in order to prevent the formation of the eutectic melt between uranium and other metals. The reactions between the uranium metal and stainless steel were tested at various conditions. And for enhancing the evaporation rate of the salt and the efficient recovery of the distilled salt, the thermal analysis of the salt distiller was conducted by using commercial CFX software. From the thermal analysis, the effect of Ar gas flow on the evaporation of the salt was studied.

Evaluation of parameters effect on the maximum fuel temperature in the core thermal and hydraulic design of HTTR

International Nuclear Information System (INIS)

Fujimoto, Nozomu; Maruyama, Soh; Sudo, Yukio; Fujii, Sadao; Niguma, Yoshinori.

1988-10-01

This report presents the results of quantitative evaluation on the effects of the dominant parameters on the maximum fuel temperature in the core thermal hydraulic design of the High Temperature Engineering Test Reactor(HTTR) of 30 MW in thermal power, 950 deg C in reactor outlet coolant temperature and 40 kg/cm 2 G in coolant pressure. The dominant parameters investigated are 1) Gap conductance. 2) Effect of eccertricity of fuel compacts in graphite sleeve. 3) Effect of spacer ribs on heat transfer coefficients. 4) Contact probability of fuel compact and graphite sleeve. 5) Validity of uniform radial power density in the fuel compacts. 6) Effect of impurity gas on gap conductance. 7) Effect of FP gas on gap conductance. The effects of these items on the maximum fuel temperature were quantitalively identified as hot spot factors. A probability of the appearance of the maximum fuel temperature was also evaluated in this report. (author)

Method for producing uranium atomic beam source

International Nuclear Information System (INIS)

Krikorian, O.H.

1976-01-01

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

Uptake of uranium from sea water by microalgae

International Nuclear Information System (INIS)

Sakaguchi, Takashi; Horikoshi, Takao; Nakajima, Akira

1978-01-01

The uptake of uranium from aqueous systems especially from sea water by various microalgae was investigated. The freshwater microalgae, Chlorella regularis, Scenedesmus bijuga, Scenedesmus chloreloides, Scenedesmus obliquus, Chlamydomonas angulosa, Chlamydomonas reinhardtii, accumulated relatively large amounts of uranium from the solution containing uranium only. The concentration factors of the above mentioned algae were: Chlorella regularis 3930, Chlamydomonas 2330 - 3400, Scenedesmus 803 - 1920. The uptake of uranium from sea water by Chlorella regularis was inhibited markedly by the co-existence of carbonate ions. Chlorella cells could take up a great quantity of uranium from decarbonated sea water. The uptake of uranium was affected by the pH of sea water, and the amount of uranium absorbed was maximum at pH 5. The experiment was carried out to screen marine microalgae which have the ability to accumulate a large amount of uranium from sea water. The uptake of uranium from sea water by marine microalgae of different species turned out to be in the following decreasing order: Synechococcus > Chlamydomonas >> Chlorella > Dunaliella > Platymonas > Calothrix > Porphyridium. The amount of uranium absorbed differed markedly with different species of marine microalgae. (author)

Large temperature variability in the southern African tropics since the Last Glacial Maximum

NARCIS (Netherlands)

Powers, L.A.; Johnson, T.C.; Werne, J.P.; Castañeda, I.S.; Hopmans, E.; Sinninghe Damsté, J.S.; Schouten, S.

2005-01-01

The role of the tropics in global climate change is actively debated, particularly in regard to the timing and magnitude of thermal and hydrological response. Continuous, high-resolution temperature records through the Last Glacial Maximum (LGM) from tropical oceans have provided much insight

Thermodynamic analysis and experimental study on the chlorination of uranium oxide by gas-solid reaction

International Nuclear Information System (INIS)

Shin, Y.J.; Kim, I.S.; Shin, H.S.; Ro, S.G.; Park, H.S.

1998-01-01

In order to determine the operating condition of an uranium chlorination process with U 3 O 8 -C-Cl 2 system, the experimental conditions have been evaluated preliminarily by the thermochemical analysis and experimentally confirmed in this study. The dry-type chlorination of U 3 O 8 occurs as irreversible and exothermic reaction and produces many kinds of chloride compounds such as UCl 3 , UCl 4 , UCl 5 , and UCl 6 in the air and humidity controlled argon environment. Taking account of Gibbs free energy and vapor pressure for various chloride compounds, the proper temperature range of chlorination appears to be 863 to 953 K in aspects of increasing reaction rate and the yield of nonvolatile product. In the course of the experimental confirmation the powder of U 3 O 8 is perfectly converted into uranium chlorides within 4 hours above 863 K, and then the maximum fraction of uranium chloride remaining in the reactor is about 30% of total conversion mass. (author)

The oxidation behaviour of uranium in air at 348-765 K

International Nuclear Information System (INIS)

Bennett, M.J.; Price, J.B.

1981-01-01

The oxidation behaviour of adjusted uranium has been examined in air, at atmospheric pressure, at 348-765 K. Particular emphasis has been directed to the role of swelling resulting from prior irradiation of the metal to a burn-up of 5600-9100 MWd/t and an addition of 2.5 x 10 4 vpm water vapour to the air. Pre-irradiation of uranium enhanced its attack by air at 348-523 K, the enhancement increasing progressively with percentage swelling. This effect resulted primarily from the break-up of the uranium surface during oxidation with the generation of a greater reaction surface area and was independent of the temperature of oxidation in dry air and also above 423 K in wet air. At lower temperatures, however, the water vapour addition increased the effective reaction rate, possibly by the transistory involvement of uranium hybride. The influence of the water vapour increased with swelling of the irradiated uranium and was greater than that exerted on the oxidation of unirradiated uranium at comparable temperatures. With increasing temperature above 623 K, swelling had a progressively decreasing influence upon the attack of irradiated uranium in both environments. (orig.)

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.

Purification by high vacuum fusion and progressive solidification of uranium from electrolytic origin; Purification par fusion sous vide eleve et solidification progressive d'uranium d'origine electrolytique

Energy Technology Data Exchange (ETDEWEB)

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

1964-01-15

grain observed, so-called secondary recrystallisation. in appendix, the method for measuring the electrical resistance by induction (with direct current)is studied from the fundamental and experimental point of view. The author applied it to the particular case of uranium for measuring the low-temperature resistance of the bars from the same which solidified first to the least pure ended the ingot. (author) [French] Dans le cadre de recherches generales sur la purification de l'uranium par fusion de zone, on a entrepris de determiner le degre de purification que l'on pourrait atteindre par une simple solidification progressive a vitesse et direction soigneusement controlees d'un uranium de purete nucleaire courante. Cet uranium de purete intermediaire fournirait un materiau de depart approprie au mode de purification ultime qu'est la fusion a zone verticale, dite ''flottante''. Dans ce but, des lingots d'uranium d'origine electrolytique ont ete refondus sous vide (2 a 5 x 10{sup -6} mm) dans une longue nacelle en UO{sub 2} apres une monte lente en temperature pour eliminer le maximum de gaz et d'impuretes volatiles. Ce degazage et cette volatilisation d'impuretes sont completes par maintien prolonge a haute temperature du bais liquide. Celui-ci est ensuite solidifie d'une extremite a l'autre de la nacelle par deplacement a vitesse lente et constante du front de solidification de facon a obtenir une repartition des impuretes selon les lois etablies par PFANN. Differentes methodes experimentales ont permis de montrer que le metal solidifie en premier lieu est nettement plus pur que celui de la partie solidifie a l'extremite opposee du lingot. Le degre de purification du metal en tete du lingot a ete apprecie, soit quantitativement par mesure du rapport des resistivites electriques a la temperature ambiante et a celle de l'azote liquide, soit qualitativement par l'examen de la structure micrographique et par l'etude de la recristallisation du metal. D'une part, le metal

Study of ammonia synthesis over uranium catalysts

International Nuclear Information System (INIS)

Spitsyn, V.I.; Erofeev, B.V.; Mikhajlenko, I.E.; Gorelkin, I.I.; Ivanov, L.S.

1980-01-01

The effect of induced radiactivity and chemical composition of uranium catalysts on their catalytic activity in the ammonia synthesis reaction has been studied. The catalyst samples comprise pieces of metal uranium and chip irradiated in nuclear reactor by the 4.3x10 16 n/cm 2 integral flux of slow neutrons. Studies of catalytic activity was carried out at 1 atm and 340-510 deg C when stoichiometric nitrogen-hydrogen mixture passed through the following installation. At different temperatures uranium nitrides of different composition are shown to be formed. Uranium nitrides with the composition close to UN 2 are the samples with the highest catalYtic activity. The reduction of catalytic activity of uranium catalysts with the increased temperature of their formation above 400 deg C is explained by low catalytic activity of forming UNsub(1.7) in comparison with UN 2 . Catalytic properties of irradiated and nonirradiated samples do not differ from one another

Some potential strategies for the treatment of waste uranium metal and uranium alloys

International Nuclear Information System (INIS)

Burns, C.J.; Frankcom, T.M.; Gordon, P.L.; Sauer, N.N.

1993-01-01

Large quantities of uranium metal chips and turnings stored throughout the DOE Complex represent a potential hazard, due to the reactivity of this material toward air and water. Methods are being sought to mitigate this by conversion of the metal, via room temperature solutions routes, to a more inert oxide form. In addition, the recycling of uranium and concomitant recovery of alloying metals is a desirable goal. The emphasis of the authors' research is to explore a variety of oxidation and reduction pathways for uranium and its compounds, and to investigate how these reactions might be applied to the treatment of bulk wastes

Determination of trace concentration of uranium in soils by the nuclear track technique

International Nuclear Information System (INIS)

Islam, G.S.; Abdullah, M.N.A.

1998-04-01

Solid state nuclear track detector CR-39 has been used to estimate trace concentration of uranium in soil and sand samples from various places of Bangladesh. Uranium contents in soil samples have been found to vary from ∼3.79 to ∼8.63 ppm and in sand samples from ∼2.39 to ∼6.53 ppm. The mean concentration in soil and in sand samples were found to be ∼4.52 and ∼2.96 ppm respectively. The maximum uranium concentration in soil samples was observed in Sylhet while the uranium concentration of sand was found to be maximum in the sea beach of Cox's Bazar. The implication of results is briefly discussed in the paper. (author)

Refining of high-temperature uranium melt by filtration through foam-ceramic filters

International Nuclear Information System (INIS)

Antsiferov, V.N.; Porozova, S.E.; Filippov, V.B.; Shtutsa, M.G.; Il'enko, E.V.; Kolotygina, N.S.

2004-01-01

An opportunity of applying foam-ceramic filters of corundum-mullite composition has been studied in refining natural uranium melts. Uranium melting conditions were chosen depending on technical characteristics of the foam ceramic filters. When their using, a portion of nonmetallic inclusions decreases by 20-30% (as little as 2.0-3.5% ingot weight), their size is reduced and their distribution in the ingot volume is equalized, contamination of uranium by the filter material being failed to be noticed. The parameters of foam-ceramic filters are optimized for provision of stable characteristics of uranium melt filtration process [ru

Evaluation of empirical relationships between extreme rainfall and daily maximum temperature in Australia

Science.gov (United States)

Herath, Sujeewa Malwila; Sarukkalige, Ranjan; Nguyen, Van Thanh Van

2018-01-01

Understanding the relationships between extreme daily and sub-daily rainfall events and their governing factors is important in order to analyse the properties of extreme rainfall events in a changing climate. Atmospheric temperature is one of the dominant climate variables which has a strong relationship with extreme rainfall events. In this study, a temperature-rainfall binning technique is used to evaluate the dependency of extreme rainfall on daily maximum temperature. The Clausius-Clapeyron (C-C) relation was found to describe the relationship between daily maximum temperature and a range of rainfall durations from 6 min up to 24 h for seven Australian weather stations, the stations being located in Adelaide, Brisbane, Canberra, Darwin, Melbourne, Perth and Sydney. The analysis shows that the rainfall - temperature scaling varies with location, temperature and rainfall duration. The Darwin Airport station shows a negative scaling relationship, while the other six stations show a positive relationship. To identify the trend in scaling relationship over time the same analysis is conducted using data covering 10 year periods. Results indicate that the dependency of extreme rainfall on temperature also varies with the analysis period. Further, this dependency shows an increasing trend for more extreme short duration rainfall and a decreasing trend for average long duration rainfall events at most stations. Seasonal variations of the scale changing trends were analysed by categorizing the summer and autumn seasons in one group and the winter and spring seasons in another group. Most of 99th percentile of 6 min, 1 h and 24 h rain durations at Perth, Melbourne and Sydney stations show increasing trend for both groups while Adelaide and Darwin show decreasing trend. Furthermore, majority of scaling trend of 50th percentile are decreasing for both groups.

Behaviour of uranium dioxide in liquid nitrogen tetraoxide

International Nuclear Information System (INIS)

Kobets, L.V.; Klavsut', G.N.; Dolgov, V.M.

1983-01-01

Interaction kinetics of uranium dioxide with liquid nitrogen tetroxide at 25-150 deg C has been studied. It is shown that in the temperature range studied NO[UO 2 (NO 3 ) 3 ] is the final product of the reaction. With the increase of specific surface of uranium dioxide and with the temperature increase the degree of oxide transformation increases. Uranium dioxide-liquid N 2 O 4 interaction proceeds in the diffusion region. Seeming activation energies and rate constants of the mentioned processes are calculated. Effect of nitrogen trioxide additions on transformation kinetics is considered

Uranium dioxide calcining apparatus

International Nuclear Information System (INIS)

Cole, E.A.; Peterson, R.S.

1978-01-01

This invention relates to an improved continuous calcining apparatus for consistently and controllably producing from calcinable reactive solid compounds of uranium, such as ammonium diuranate, uranium dioxide (UO 2 ) having an oxygen to uranium ratio of less than 2.2. The apparatus comprises means at the outlet end of a calciner kiln for receiving hot UO 2 , means for cooling the UO 2 to a temperature of below 100 deg C and conveying the cooled UO 2 to storage or to subsequent UO 2 processing apparatus where it finally comes into contact with air, the means for receiving cooling and conveying being sealed to the outlet end of the calciner and being maintained full of UO 2 and so operable as to exclude atmospheric oxygen from coming into contact with any UO 2 which is at elevated temperatures where it would readily oxidize, without the use of extra hydrogen gas in said means. (author)

METHOD OF HOT ROLLING URANIUM METAL

Science.gov (United States)

Kaufmann, A.R.

1959-03-10

A method is given for quickly and efficiently hot rolling uranium metal in the upper part of the alpha phase temperature region to obtain sound bars and sheets possessing a good surface finish. The uranium metal billet is heated to a temperature in the range of 1000 deg F to 1220 deg F by immersion iii a molten lead bath. The heated billet is then passed through the rolls. The temperature is restored to the desired range between successive passes through the rolls, and the rolls are turned down approximately 0.050 inch between successive passes.

Electrical impedance studies of uranium oxide

International Nuclear Information System (INIS)

Hampton, R.N.

1986-11-01

The thesis presents data on the electrical properties of uranium oxide at temperatures from 1700K to 4.2K, and pressures between 25 K bar and 70 K bar. The impedance data were analysed using the technique of complex plane representation to establish the conductivity and dielectric constant of uranium dioxide. The thermophysical data were compared with previously reported experimental and theoretical work on uranium dioxide and other fluorite structured oxides. (U.K.)

Synthesis of UN coatings on uranium

International Nuclear Information System (INIS)

Mar, R.W.; Hastings, J.C.

1975-04-01

A single-displacement reaction approach was used to form uranium mononitride as a protective coating for uranium; the source of the nitrogen was a solid nitride, and magnesium nitride was chosen as the most attractive candidate for the experiment. While the goal of synthesizing a single-phase uranium mononitride coating at temperatures lower than 1405 K was met, a number of problems inherent in the process were identified. 6 figures, 2 tables

Maruhn-Greiner Maximum of Uranium Fission for Confirmation of Low Energy Nuclear Reactions LENR via a Compound Nucleus with Double Magic Numbers

Science.gov (United States)

Hora, H.; Miley, G. H.

2007-12-01

One of the most convincing facts about LENR due to deuterons of very high concentration in host metals as palladium is the measurement of the large scale minimum of the reaction probability depending on the nucleon number A of generated elements at A = 153 where a local maximum was measured. This is similar to the fission of uranium at A = 119 where the local maximum follows from the Maruhn-Greiner theory if the splitting nuclei are excited to about MeV energy. The LENR generated elements can be documented any time after the reaction by SIMS or K-shell X-ray excitation to show the very unique distribution with the local maximum. An explanation is based on the strong Debye screening of the Maxwellian deuterons within the degenerate rigid electron background especially within the swimming electron layer at the metal surface or at interfaces. The deuterons behave like neutrals at distances of about 2 picometers. They may form clusters due to soft attraction in the range above thermal energy. Clusters of 10 pm diameter may react over long time probabilities (megaseconds) with Pd nuclei leading to a double magic number compound nucleus which splits like in fission to the A = 153 element distribution.

Uranium oxide recovering method

International Nuclear Information System (INIS)

Ota, Kazuaki; Takazawa, Hiroshi; Teramae, Naoki; Onoue, Takeshi.

1997-01-01

Nitrates containing uranium nitrate are charged in a molten salt electrolytic vessel, and a heat treatment is applied to prepare molten salts. An anode and a cathode each made of a graphite rod are disposed in the molten salts. AC voltage is applied between the anode and the cathode to conduct electrolysis of the molten salts. Uranium oxides are deposited as a recovered product of uranium, on the surface of the anode. The nitrates containing uranium nitrate are preferably a mixture of one or more nitrates selected from sodium nitrate, potassium nitrate, calcium nitrate and magnesium nitrate with uranium nitrate. The nitrates may be liquid wastes of nitrates. The temperature for the electrolysis of the molten salts is preferably from 150 to 300degC. The voltage for the electrolysis of the molten salts is preferably an AC voltage of from 2 to 6V, more preferably from 4 to 6V. (I.N.)

Drawing of uranium in γ phase

International Nuclear Information System (INIS)

Stohr, J.A.

1955-01-01

It describes the study of working and drawing of uranium in γ phase. In a first part, the forgeable characteristics of uranium metal in the three different phases (α, β and γ) are compared by using BASTIEN-PORTEVIN method. The different experiments are testing the behaviour metal in each phase under different stresses and a temperature gradient as slow and shock traction, slow and shock compression, resilience, flexibility. Results show that optimum conditions for uranium drawing is uranium in phase γ. In a second part, it described the drawing method and process. The uranium rods obtained by this technique are of very good quality. In addition, the material wear is very low which permits a low production cost. Finally, the uranium rod physical properties are studied. (M.P.)

Carbon diffusion in molten uranium: an ab initio molecular dynamics study

Science.gov (United States)

Garrett, Kerry E.; Abrecht, David G.; Kessler, Sean H.; Henson, Neil J.; Devanathan, Ram; Schwantes, Jon M.; Reilly, Dallas D.

2018-04-01

In this work we used ab initio molecular dynamics within the framework of density functional theory and the projector-augmented wave method to study carbon diffusion in liquid uranium at temperatures above 1600 K. The electronic interactions of carbon and uranium were described using the local density approximation (LDA). The self-diffusion of uranium based on this approach is compared with literature computational and experimental results for liquid uranium. The temperature dependence of carbon and uranium diffusion in the melt was evaluated by fitting the resulting diffusion coefficients to an Arrhenius relationship. We found that the LDA calculated activation energy for carbon was nearly twice that of uranium: 0.55 ± 0.03 eV for carbon compared to 0.32 ± 0.04 eV for uranium. Structural analysis of the liquid uranium-carbon system is also discussed.

Specific features of the WWER Uranium-Gadolinium fuel behavior at BOL

International Nuclear Information System (INIS)

Shcheglov, A.; Proselkov, V.; Volkov, B.

2013-01-01

The calculated-experimental analysis of the WWER fuel behavior with 5%wt of gadolinium oxide at the beginning of life (BOL) is presented. The results are based on the data on fuel centerline temperature measurements, gas media pressure inside the cladding and fuel elongation obtained during irradiation of the test fuel rods in HBWR (Halden). Computer analysis of experimental data is performed with TOPRA-2, version 2 code. It is shown that specific features of the uranium-gadolinium fuel behavior at the early of life is due to presence of burnable absorber influencing the average linear heat rating, radial power distribution and lower thermal conductivity. In particular, the analysis of “late” relocation effect on the maximum Gd fuel temperature is presented. (authors)

Uranium and radon surveys in western Himalaya

International Nuclear Information System (INIS)

Virk, H.S.

1997-01-01

The water samples from mountain springs, streams and river systems in the western Himalaya were collected and analysed in the laboratory for uranium and radon contents. It is observed that the Himalayan river system is conspicuous by its high dissolved uranium and radium concentration. The water samples contain from 0.89 ppb to 63.4 ppb of uranium and from 34 Bq/I to 364 Bq/I of radon. The radon emanation in soil is measured by the track-etch method, emanometry and alpha-logger technique. The daily and long-term variation of radon was monitored in some mineralized zones of Himachal Pradesh (HP) state with high uranium content in the soil. The maximum values of radon are recorded in Chhinjra, Rameda, Samurkala and Kasol areas of HP. (author)

Oxidation experiment of metal uranium waste for the treatment of depleted uranium waste

International Nuclear Information System (INIS)

Kang, K. H.; Kwac, K. I.; Kim, K. J.

2001-01-01

A study was conducted on the oxidation behavior of U-Ti chips(Depleted Uranium, DU chips) using an XRD and a thermogravimetric analyzer in the temperature range from 250 to 500 .deg. C in air. At the temperature lower than 400 .deg. C, DU chips were converted to UO 2 , U 3 O 7 and U 3 O 8 whereas at the temperature higher than 400 .deg. C, DU chips were completely converted to U 3 O 8 , the most stable form of uranium oxide. The activation energy for the oxidation of U-Ti chips is found, 44.9 kJ/mol and the oxidation rate in terms of weight gain (%) can be expressed as ; dW/dt=8.4 x 10 2 e(-44.9 kJ/mol /RT) wt %/min (250≤T(deg. C)≤500) where W=weight gain (%), t=time and T=temperature

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

Energy Technology Data Exchange (ETDEWEB)

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

1965-07-01

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

Methods for the exploration and recovering of uranium

International Nuclear Information System (INIS)

Kegel, K.E.

1982-01-01

The uranium reserves in the western world occur basically in two types of deposits a) vein type and vein like types b) sedimentary types, with the vein deposits providing only 5 percent of the actual uranium production. 85% of the known uranium reserves in the western world, amounting to about 5 million metric tons U occur in a relatively small number of countries (U.S.A., Canada, Australia, South Africa and Namibia, France, Niger and Gabun). Exploration on uranium deposits is carried out by using geophysical and geochemical methods. Radiometry, i.e. the determination of the radioactivity of the ground in a prospective area, is the main geophysical tool. In the mining of uranium ores, practically all mining methods, applied in other metal mining branches, are being used. The benefication of uranium ore is characterized by a large up-grading factor (i.e. the ratio between the uranium content in the concentrates and the uranium content in the ore) which is higher than in most other metal mining operations. In the field of health and safety in uranium mines, the radiation protection of the workers plays a paramount role. Strict rules exist for maximum values of certain elements in waste air and waste water of uranium mining operations, emitted into the environment. (orig.)

Reaction between uranium hexafluoride and trimethylsilylhalides

Energy Technology Data Exchange (ETDEWEB)

Brown, D; Berry, J A [UKAEA Atomic Energy Research Establishment, Harwell. Chemistry Div.; Holloway, J H; Staunton, G M [Leicester Univ. (UK). Dept. of Chemistry

1938-07-01

Reactions involving 1.1:1 molar ratios of uranium hexafluoride to either trimethylsilylchloride or trimethylsilylbromide in halocarbon solutions yield ..beta..-UF/sub 5/ at room temperature. With 2 mol equivalents of trimethylsilylchloride the product is UF/sub 4/. The reactions appear to proceed via the intermediate formation of unstable brown uranium(VI) chloride and bromide fluorides. Calculations show that UClF/sub 5/ and UCl/sub 2/F/sub 4/ are thermodynamically unstable with respect to the loss of chlorine at room temperature.

Biosorption of uranium and lead by Streptomyces longwoodensis

International Nuclear Information System (INIS)

Friis, N.; Myers-Keith, P.

1986-01-01

Biosorption of uranium and lead by lyophilized cells of Streptomyces longwoodensis was examined as a function of metal concentration, pH, cell concentration, and culture age. Cells harvested from the stationary growth phase exhibited an exceptionally high capacity for uranium (0.44 g U/g dry weight) at pH 5. Calculated values of the distribution coefficient and separation factor indicated a strong preference of the cell mass for uranyl ions over lead ions. The specific uranium uptake was similar for the cell wall and the cytoplasmic fraction. Uranium uptake was associated with an increase in hydrogen ion concentration, and phosphorus analysis of whole cells indicated a simple stoichiometric ratio between uranium uptake and phosphorus content. It is proposed that metal ions are bound to phosphodiester residues present both in the cell wall and cytoplasmic fractions. Based on this model, it was shown that uranium accumulation exhibits a maximum at pH 4.6 that is supported by experimental data from previous investigations

Magnesium and uranium ignition in different gaseous atmospheres; Inflammabilite du magnesium et de l'uranium dans l'air et le gaz carbonique

Energy Technology Data Exchange (ETDEWEB)

Darras, R; Baque, P; Leclercq, D [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

1960-07-01

Magnesium, uranium and some of their alloys burning temperatures have been systematically determined in an air or carbon dioxide atmosphere, either dry or wet. Two different ways of heating have been used: either continuously rising up the temperature, or heating to and then maintaining a constant temperature. The results are clearly different in the two cases. Besides, if moisture has little effect on the magnesium burning temperatures in air, it does lower them by about 130-140 deg. C in CO{sub 2}. The differences of sight between the burning of magnesium and uranium have been noticed; this leads to distinguish between an 'ignition' and an 'inflammation'. (author) [French] Les temperatures auxquelles apparait la combustion vive du magnesium, de l'uranium et certains de leurs alliages ont ete determinees systematiquement dans l'air et le gaz carbonique, soit secs, soit humidifies. On a mis en evidence l'influence du mode de chauffage sur les resultats: soit montee en temperature continue, soit stabilisation a partir d'une certaine temperature. En outre, si la presence d'humidite affecte peu les temperatures de combustion vive du magnesium dans l'air, elle les abaisse de 130 a 140 deg. C dans le gaz carbonique. Les differences d'aspect entre la combustion vive du magnesium et de l'uranium ont egalement ete remarquees, ce qui amene notamment a distinguer une 'ignition' d'une 'inflammation'. (auteur)

Temperature of maximum density and excess thermodynamics of aqueous mixtures of methanol

Energy Technology Data Exchange (ETDEWEB)

González-Salgado, D.; Zemánková, K. [Departamento de Física Aplicada, Universidad de Vigo, Campus del Agua, Edificio Manuel Martínez-Risco, E-32004 Ourense (Spain); Noya, E. G.; Lomba, E. [Instituto de Química Física Rocasolano, CSIC, Calle Serrano 119, E-28006 Madrid (Spain)

2016-05-14

In this work, we present a study of representative excess thermodynamic properties of aqueous mixtures of methanol over the complete concentration range, based on extensive computer simulation calculations. In addition to test various existing united atom model potentials, we have developed a new force-field which accurately reproduces the excess thermodynamics of this system. Moreover, we have paid particular attention to the behavior of the temperature of maximum density (TMD) in dilute methanol mixtures. The presence of a temperature of maximum density is one of the essential anomalies exhibited by water. This anomalous behavior is modified in a non-monotonous fashion by the presence of fully miscible solutes that partly disrupt the hydrogen bond network of water, such as methanol (and other short chain alcohols). In order to obtain a better insight into the phenomenology of the changes in the TMD of water induced by small amounts of methanol, we have performed a new series of experimental measurements and computer simulations using various force fields. We observe that none of the force-fields tested capture the non-monotonous concentration dependence of the TMD for highly diluted methanol solutions.

Uranium leaching using mixed organic acids produced by Aspergillus niger

International Nuclear Information System (INIS)

Yong-dong Wang; Guang-yue Li; De-xin Ding; Zhi-xiang Zhou; Qin-wen Deng; Nan Hu; Yan Tan

2013-01-01

Both of culture temperature and pH value had impacts on the degree of uranium extraction through changing types and concentrations of mixed organic acids produced by Aspergillus niger, and significant interactions existed between them though pH value played a leading role. And with the change of pH value of mixed organic acids, the types and contents of mixed organic acids changed and impacted on the degree of uranium extraction, especially oxalic acid, citric acid and malic acid. The mean degree of uranium extraction rose to peak when the culture temperature was 25 deg C (76.14 %) and pH value of mixed organic acids was 2.3 (82.40 %) respectively. And the highest one was 83.09 %. The optimal culture temperature (25 deg C) of A. niger for uranium leaching was different from the most appropriate growing temperature (37 deg C). (author)

ELECTRODEPOSITION OF NICKEL ON URANIUM

Science.gov (United States)

Gray, A.G.

1958-08-26

A method is described for preparing uranium objects prior to nickel electroplating. The process consiats in treating the surface of the uranium with molten ferric chloride hexahydrate, at a slightiy elevated temperature. This treatment etches the metal surface providing a structure suitable for the application of adherent electrodeposits and at the same time plates the surface with a thin protective film of iron.

Phonon dispersion relation of uranium nitrate above and below the Neel temperature

International Nuclear Information System (INIS)

Dolling, G.; Holden, T.M.; Evensson, E.C.; Buyers, W.J.L.; Lander, G.H.

1977-01-01

Neutron coherent inelastic scattering measurements have been made of the phonon dispersion relation of uranium nitride both above and below the Neel temperature T/sub N/ = 50 K. Within the precision of the measurements, about 1% in frequency and 10% in line width and in scattered neutron intensity, no significant changes in these phonon properties were observed as a function of temperature other than those arising from population factor changes and a small stiffening of the lattice as the temperature decreases. At 4.2 K, two acoustic and two optic branches have been determined for each of the [001], [110] and [111] directions. The optic mode measurements revealed (a) a 20% variation in frequency across the Brillouin zone and (b) an interesting disposition of the LO and TO modes, such that nu/sub LO/ > nu/sub TO/ along [001] and [110], while the reverse is true along the [111] directions. Within the experimental resolution, the LO and TO modes are degenerate near q = 0. We have been unable to obtain any satisfactory description of these results on the basis of conventional theoretical treatments (e.g. rigid-ion or shell models). Other possible interpretations of the results are discussed

Phonon dispersion relation of uranium nitride above and below the Neel temperature

International Nuclear Information System (INIS)

Dolling, G.; Holden, T.M.; Svensson, E.C.; Buyers, W.J.L.; Lander, G.H.

1977-01-01

Neutron coherent inelastic scattering measurements have been made of the phonon dispersion relation of uranium nitride both above and below the Neel temperature T N = 50 K. Within the precision of the measurements, about 1% in frequency and 10% in line width and in scattered neutron intensity, no significant changes in these phonon properties were observed as a function of temperature other than those arising from population factor changes and a small stiffening of the lattice as the temperature decreases. At 4.2 K, two acoustic and two optic branches have been determined for each of the [001], [110] and [111] directions. The optic mode measurements revealed (a) a 20% variation in frequency across the Brillouin zone and (b) and interesting disposition of the LO and TO modes, such that ν LO > ν TO along [001] and [11-], while the reverse is true along the [111] directions. Within the experimental resolution, the LO and TO modes are degenerate near q = 0. We have been unable to obtain any satisfactory description of these results on the basis of conventional theoretical treatments (e.g. rigid-ion or shell models). Other possible interpretations of the results are discussed. (author)

An X-ray photoelectron spectroscopic study of a nitric acid/argon ion cleaned uranium metal surface at elevated temperature

International Nuclear Information System (INIS)

Paul, A.J.; Sherwood, P.M.A.

1987-01-01

X-ray photoelectron spectroscopy has been used to study the surface of uranium metal cleaned by nitric acid treatment and argon ion etching, followed by heating in a high vacuum. The surface is shown to contain UOsub(2-x) species over the entire temperature range studied. Heating to temperatures in the range 400-600 0 C generates a mixture of this oxide, the metal and a carbide and/or oxycarbide species. (author)

Internal friction in uranium

International Nuclear Information System (INIS)

Selle, J.E.

1975-01-01

Results are presented of studies conducted to relate internal friction measurements in U to allotropic transformations. It was found that several internal friction peaks occur in α-uranium whose magnitude changed drastically after annealing in the β phase. All of the allotropic transformations in uranium are diffusional in nature under slow heating and cooling conditions. Creep at regions of high stress concentration appears to be responsible for high temperature internal friction in α-uranium. The activation energy for grain boundary relaxation in α-uranium was found to be 65.1 +- 4 kcal/mole. Impurity atoms interfere with the basic mechanism for grain boundary relaxation resulting in a distribution in activation energies. A considerable distribution in ln tau 0 was also found which is a measure of the distribution in local order and in the Debye frequency around a grain boundary

Simultaneous analysis of uranium and nitrate

Energy Technology Data Exchange (ETDEWEB)

Bostick, D.T.

1978-04-01

A direct spectrophotometric method has been developed for the determination of 20 to 200 g/l of uranium in the presence of 3 to 5 M nitric acid. A dual-wavelength analysis is used to eliminate the enhancing effect of nitrate ion on the uranium visible spectra. The precision and accuracy of the simultaneous analysis of uranium and nitrate were compared using combinations of the four uranium wavelength maxima, occurring at 426, 416, 403 and 359 nm. Calculations based on 426 and 416 nm data yielded the most accurate results. The calculated relative standard deviation of uranium and nitrate concentrations was 5.4 percent and 15.5 percent, respectively. The photometric procedure is slightly affected by temperature; an increase of one degree centigrade results in a 0.2 g/l overestimation of uranium concentration. Because the method is non-destructive, it is directly applicable to the continuous in-line analysis of dissolved uranium in aqueous fuel reprocessing streams.

Reoxidation of uranium in electrolytically reduced simulated oxide fuel during residual salt distillation

International Nuclear Information System (INIS)

Eun-Young Choi; Jin-Mok Hur; Min Ku Jeon; University of Science and Technology, Yuseong-gu, Daejeon

2017-01-01

We report that residual salt removal by high-temperature distillation causes partial reoxidation of uranium metal to uranium oxide in electrolytically reduced simulated oxide fuel. Specifically, the content of uranium metal in the above product decreases with increasing distillation temperatures, which can be attributed to reoxidation by Li 2 O contained in residual salt (LiCl). Additionally, we estimate the fractions of Li 2 O reacted with uranium metal under these conditions, showing that they decrease with decreasing temperature, and calculate some thermodynamic parameters of the above reoxidation. (author)

New England observed and predicted August stream/river temperature maximum daily rate of change points

Data.gov (United States)

U.S. Environmental Protection Agency — The shapefile contains points with associated observed and predicted August stream/river temperature maximum negative rate of change in New England based on a...

New England observed and predicted Julian day of maximum growing season stream/river temperature points

Data.gov (United States)

U.S. Environmental Protection Agency — The shapefile contains points with associated observed and predicted Julian day of maximum growing season stream/river temperatures in New England based on a spatial...

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

Experimental study on uranium alloys for hydrogen storage

International Nuclear Information System (INIS)

Deaconu, M.; Meleg, T.; Dinu, A.; Mihalache, M.; Ciuca, I.; Abrudeanu, M.

2013-01-01

The heaviest isotope of hydrogen is one of critically important elements in the field of fusion reactor technology. Conventionally, uranium metal is used for the storage of heavier isotopes of hydrogen (D and T). Under appropriate conditions, uranium absorbs hydrogen to form a stable UH 3 compound when exposed to molecular hydrogen at the temperature range of 300-500 O C at varied operating pressure below one atmosphere. However, hydriding-dehydriding on pure uranium disintegrates the specimen into fine powder. The powder is highly pyrophoric and has low heat conductivity, which makes it difficult to control the temperature, and has a high possibility of contamination Due to the powdering effect as hydrogen in uranium, alloying uranium with other metal looks promising for the use of hydrogen storage materials. This paper has the aim to study the hydriding properties of uranium alloys, including U-Ti U-Mo and U-Ni. The uranium alloys specimens were prepared by melting the constituent elements by means of simultaneous measurements of thermo-gravimetric and differential thermal analyses (TGA-DTA) and studied in as cast condition as hydrogen storage materials. Then samples were thermally treated under constant flow of hydrogen, at various temperatures between 573-973 0 K. The structural and absorption properties of the products obtained were examined by thermo-gravimetric analysis (TG), X-ray diffraction (XRD) and scanning electron microscopy (SEM). They slowly reacted with hydrogen to form the ternary hydride and the hydrogenated samples mainly consisted of the pursued ternary hydride bat contained also U or UO 2 and some transient phase. (authors)

Buckling and reaction rate experiments in plutonium/uranium metal fuelled, graphite moderated lattices at temperatures up to 400 deg. C. Part I: Experimental techniques and results

Energy Technology Data Exchange (ETDEWEB)

Carter, D H; Clarke, W G; Gibson, M; Hobday, R; Hunt, C; Marshall, J; Puckett, B J; Symons, C R; Wass, T [General Reactor Physics Division, Atomic Energy Establishment, Winfrith, Dorchester, Dorset (United Kingdom)

1964-07-15

This report presents experimental measurements of bucklings, flux fine structure and fission rate distributions in graphite moderated lattices fuelled with plutonium/uranium metal at temperatures up to 400 deg. C in the sub-critical assemblies SCORPIO I and SCORPIO II. The experimental techniques employed are described in some detail. The accuracy of the experimental measurements appears to be adequate for testing methods of calculation being developed for the calculation of reactivity and temperature coefficient of reactivity for power reactors containing plutonium and uranium. (author) 26 refs, 17 tabs, 17 figs

Characteristics of chlorites from Huangnihu uranium deposit and their implications in uranium metallogenic environment in the southern part of Jiangxi Province

International Nuclear Information System (INIS)

Hu Zhihua; Lin Jinrong; Pang Yaqing; Gao Fei; Rong Jiashu; Guo Shuying

2013-01-01

Chlorite is genetically related to uranium mineralization in Huangnihu uranium deposit. By means of microscopic and electronic microprobe analysis, the authors investigated chemical composition and texture of the chlorite and found that chlorite in Huangnihu deposit has the following characteristics: 1. they are mainly Fe-rich chlorite composed of chamosite and brunsvigite, of which chemical composition is mainly affected by mud and mafic rock; 2. the Fe-Mg and Al"I"V-Si substitution dominates the octahedral substitution supplemented by Al"V"I-Fe substitution; the oolitic chlorite and biotite feinted chlorite closely associated with uranium were formed at temperatures of 216.23 ∼ 256.73℃ (average 228.6℃). The chemical composition and forming environment of the oolitic chlorite and biotite illusion chlorite suggests that Huangnihu uranium deposit is a low-moderate temperature hydrothermal uranium deposit formed in a reducing environment and iron-rich formation, the ore-forming fluid mainly originated from shale rock, partly from ultramafic or mafic liquid. (authors)

Application of Markov chain model to daily maximum temperature for thermal comfort in Malaysia

International Nuclear Information System (INIS)

Nordin, Muhamad Asyraf bin Che; Hassan, Husna

2015-01-01

The Markov chain’s first order principle has been widely used to model various meteorological fields, for prediction purposes. In this study, a 14-year (2000-2013) data of daily maximum temperatures in Bayan Lepas were used. Earlier studies showed that the outdoor thermal comfort range based on physiologically equivalent temperature (PET) index in Malaysia is less than 34°C, thus the data obtained were classified into two state: normal state (within thermal comfort range) and hot state (above thermal comfort range). The long-run results show the probability of daily temperature exceed TCR will be only 2.2%. On the other hand, the probability daily temperature within TCR will be 97.8%

Analysis of trace uranium in human urine by using the fission track method

International Nuclear Information System (INIS)

Chen Huailu; Yang Huazhang; Zhao Dongzhi; Wang Kaixue

1988-01-01

In order to know the contents of uranium in human urine, urine samples from 10 healthy persons with different ages and sexes in Lanzhou area were analysed with the fisson track method. The results, in contrast with the contents of uranium in Yellow River water (in Lanzhou section), tap-water and rainwater, indicated that the content of uranium in human urine was lower than that in tap-water. From the ratio of uranium in human urine to that in tap-water, the maximum excreted rate of uranium from urine is evaluated to be 42.2%

Of floating-zone uranium; Sur l'uranium de zone flottante

Energy Technology Data Exchange (ETDEWEB)

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

1965-01-01

The floating zone method has been chosen in order to purify uranium. The various parameters occurring in this purification technique, have been studied theoretically and technologically. The speed that proves to be the most efficient is 0,7 cm/h, the direction can only upwards, and the fusion must take place under pressure of 10{sup -7} Torr or so. Besides such problems concerning purification, the study of the floating zone stability led us to define a field touching the size and diameter of uranium drops, which, on the one hand coincides with Heywang's conditions and, on the other hand, is compatible with a fusion in the core of the bar. Such field shows that the floating zone can easily apply to bars whose diameter is included between 5 and 10 mm, and that it cannot work out when the diameter exceeds 21 mm. The apparatus, consisting in a means of heating by electronic bombardment under ultra-vacuum is conditioned by the various parameters that have been studied. As the analysis results were insufficient, the uranium thus dealt with has been characterized by metallurgic and physical tests: micrographic tests, measures of microhardness, measures of electric resistivity at a low temperature, have shown a definite purification at the bar-head; these results have been confirmed by the lowering at 270 C of the temperature of recrystallization together with the definite tendency of the refined metal to polygonize. The measures of electric resistivity constitute an easy and quantitative way of figuring out the metal purity. The influence of an impurity on the electric resistivity of uranium has been studied by U-Au alloys with a weak concentration of gold. The two important following points are brought out be these experiences: 1 - the measure of electric resistivity should be worked out on anneal bars in {gamma} phase and cooled. 2 - Gold has a very strong influence on uranium; the value 500 {mu}{omega}cm per cent of gold enabled us to give a total concentration of 20

Development of a high density fuel based on uranium-molybdenum alloys with high compatibility in high temperatures

International Nuclear Information System (INIS)

Oliveira, Fabio Branco Vaz de

2008-01-01

This work has as its objective the development of a high density and low enriched nuclear fuel based on the gamma-UMo alloys, for utilization where it is necessary satisfactory behavior in high temperatures, considering its utilization as dispersion. For its accomplishment, it was started from the analysis of the RERTR ('Reduced Enrichment for Research and Test Reactors') results and some theoretical works involving the fabrication of gamma-uranium metastable alloys. A ternary addition is proposed, supported by the properties of binary and ternary uranium alloys studied, having the objectives of the gamma stability enhancement and an ease to its powder fabrication. Alloys of uranium-molybdenum were prepared with 5 to 10% Mo addition, and 1 and 3% of ternary, over a gamma U7Mo binary base alloy. In all the steps of its preparation, the alloys were characterized with the traditional techniques, to the determination of its mechanical and structural properties. To provide a process for the alloys powder obtention, its behavior under hydrogen atmosphere were studied, in thermo analyser-thermo gravimeter equipment. Temperatures varied from the ambient up to 1000 deg C, and times from 15 minutes to 16 hours. The results validation were made in a semi-pilot scale, where 10 to 50 g of powders of some of the alloys studied were prepared, under static hydrogen atmosphere. Compatibility studies were conducted by the exposure of the alloys under oxygen and aluminum, to the verification of possible reactions by means of differential thermal analysis. The alloys were exposed to a constant heat up to 1000 deg C, and their performances were evaluated in terms of their reaction resistance. On the basis of the results, it was observed that ternary additions increases the temperatures of the reaction with aluminum and oxidation, in comparison with the gamma UMo binaries. A set of conditions to the hydration of the alloys were defined, more restrictive in terms of temperature, time and

Analyses of uranium series nuclides by alpha spectrometer on the uranium deposit

International Nuclear Information System (INIS)

Wismawati, T.

2000-01-01

The research is one of the program which was planned by PNC (Power Reactor and Nuclear Fuel Development Corporation). In this research the analyses of the uranium series nuclide of rock samples from uranium Tono deposit, Japan have been carried out. The 17 samples were collected from Tsukiyoshi Fault, at Gallery X on Shaft 2 consist of granite, sedimentary rocks and fault area. The aim of the research is to determine the area of U accumulation, equilibrium and leaching. The samples were treated by chemical reagent, separated by ion exchange resin and extracted by organic compounds. The uranium and thorium were deposited on the stainless steel plate surface by the electrolysis process. The activity of uranium and thorium was determined by alpha spectrometer. From the analyses data have been obtained that shows that the maximum activity of 238 U is 3.6798±0.1873 Bq/g, activity 234 U is 3.5450±0.1805 Bq/g and activity 230 Th is 3.6720±0.1868 Bq/g. The ratio figure 234 U/ 238 U versus 2 34 U / 2 30 T h has been drawn. As the conclusion, 6 samples point (No.3, 5, 8, 11, 13 and 16) lied in or on the boundary of the uranium accumulation area, 7 samples (No. 4, 6, 9, 10, 12, 15 and 17) are very close to the equilibrium position, 4 points (No. 1, 2, 7, and 14) in the leaching process. (author)

Hot pressing of uranium nitride and mixed uranium plutonium nitride

International Nuclear Information System (INIS)

Chang, J.Y.

1975-01-01

The hot pressing characteristics of uranium nitride and mixed uranium plutonium nitride were studied. The utilization of computer programs together with the experimental technique developed in the present study may serve as a useful purpose of prediction and fabrication of advanced reactor fuel and other high temperature ceramic materials for the future. The densification of nitrides follow closely with a plastic flow theory expressed as: d rho/ dt = A/T(t) (1-rho) [1/1-(1-rho)/sup 2/3/ + B1n (1-rho)] The coefficients, A and B, were obtained from experiment and computer curve fitting. (8 figures) (U.S.)

Radiation damage of metal uranium; Radijaciono ostecenje metalnog urana

Energy Technology Data Exchange (ETDEWEB)

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

1965-11-15

This report is concerned with the role of dispersion second phase in uranium and burnup rate. The role of dispersion phases in radiation stability of metal uranium was studies by three methods: variation of electric conductivity dependent on the neutron flux and temperature of pure uranium for different states of dispersion second phase; influence of dispersion phase on the radiation creep; transmission electron microscopy of fresh and irradiated uranium.

Effect of uranium (VI) on two sulphate-reducing bacteria cultures from a uranium mine site

International Nuclear Information System (INIS)

Martins, Monica; Faleiro, Maria Leonor; Chaves, Sandra; Tenreiro, Rogerio; Costa, Maria Clara

2010-01-01

This work was conducted to assess the impact of uranium (VI) on sulphate-reducing bacteria (SRB) communities obtained from environmental samples collected on the Portuguese uranium mining area of Urgeirica. Culture U was obtained from a sediment, while culture W was obtained from sludge from the wetland of that mine. Temperature gradient gel electrophoresis (TGGE) was used to monitor community changes under uranium stress conditions. TGGE profiles of dsrB gene fragment demonstrated that the initial cultures were composed of SRB species affiliated with Desulfovibrio desulfuricans, Desulfovibrio vulgaris and Desulfomicrobium spp. (sample U), and by species related to D. desulfuricans (sample W). A drastic change in SRB communities was observed as a result of uranium (VI) exposure. Surprisingly, SRB were not detected in the uranium removal communities. Such findings emphasize the need of monitoring the dominant populations during bio-removal studies. TGGE and phylogenetic analysis of the 16S rRNA gene fragment revealed that the uranium removal consortia are composed by strains affiliated to Clostridium genus, Caulobacteraceae and Rhodocyclaceae families. Therefore, these communities can be attractive candidates for environmental biotechnological applications associated to uranium removal.

Biosorption of uranium by cross-linked and alginate immobilized residual biomass from distillery spent wash

International Nuclear Information System (INIS)

Bustard, M.; McHale, A.P.

1997-01-01

Residual biomass from a whiskey distillery was examined for its ability to function as a biosorbent for uranium. Biomass recovered and lyophilised exhibited a maximum biosorption capacity of 165-170 mg uranium/g dry weight biomass at 15 C. With a view towards the development of continuous or semi-continuous flow biosorption processes it was decided to immobilize the material by (1) cross-linking with formaldehyde and (2) introducing that material into alginate matrices. Cross-linking the recovered biomass resulted in the formation of a biosorbent preparation with a maximum biosorption capacity of 185-190 mg/g dry weight biomass at 15 C. Following immobilization of biomass in alginate matrices it was found that the total amount of uranium bound to the matrix did not change with increasing amounts of biomass immobilized. It was found however, that the proportion of uranium bound to the biomass within the alginate-biomass matrix increased with increasing biomass concentration. Further analysis of these preparations demonstrated that the alginate-biomass matrix had a maximum biosorption capacity of 220 mg uranium/g dry weight of the matrix, even at low concentrations of biomass. (orig.). With 3 figs., 1 tab

Biosorption of uranium by cross-linked and alginate immobilized residual biomass from distillery spent wash

Energy Technology Data Exchange (ETDEWEB)

Bustard, M. [Biotechnology Research Group, School of Applied Biological and Chemical Sciences, University of Ulster, Coleraine (United Kingdom); McHale, A.P. [Biotechnology Research Group, School of Applied Biological and Chemical Sciences, University of Ulster, Coleraine (United Kingdom)

1997-08-01

Residual biomass from a whiskey distillery was examined for its ability to function as a biosorbent for uranium. Biomass recovered and lyophilised exhibited a maximum biosorption capacity of 165-170 mg uranium/g dry weight biomass at 15 C. With a view towards the development of continuous or semi-continuous flow biosorption processes it was decided to immobilize the material by (1) cross-linking with formaldehyde and (2) introducing that material into alginate matrices. Cross-linking the recovered biomass resulted in the formation of a biosorbent preparation with a maximum biosorption capacity of 185-190 mg/g dry weight biomass at 15 C. Following immobilization of biomass in alginate matrices it was found that the total amount of uranium bound to the matrix did not change with increasing amounts of biomass immobilized. It was found however, that the proportion of uranium bound to the biomass within the alginate-biomass matrix increased with increasing biomass concentration. Further analysis of these preparations demonstrated that the alginate-biomass matrix had a maximum biosorption capacity of 220 mg uranium/g dry weight of the matrix, even at low concentrations of biomass. (orig.). With 3 figs., 1 tab.

The Hengill geothermal area, Iceland: Variation of temperature gradients deduced from the maximum depth of seismogenesis

Science.gov (United States)

Foulger, G. R.

1995-04-01

Given a uniform lithology and strain rate and a full seismic data set, the maximum depth of earthquakes may be viewed to a first order as an isotherm. These conditions are approached at the Hengill geothermal area S. Iceland, a dominantly basaltic area. The likely strain rate calculated from thermal and tectonic considerations is 10 -15 s -1, and temperature measurements from four drill sites within the area indicate average, near-surface geothermal gradients of up to 150 °C km -1 throughout the upper 2 km. The temperature at which seismic failure ceases for the strain rates likely at the Hengill geothermal area is determined by analogy with oceanic crust, and is about 650 ± 50 °C. The topographies of the top and bottom of the seismogenic layer were mapped using 617 earthquakes located highly accurately by performing a simultaneous inversion for three-dimensional structure and hypocentral parameters. The thickness of the seismogenic layer is roughly constant and about 3 km. A shallow, aseismic, low-velocity volume within the spreading plate boundary that crosses the area occurs above the top of the seismogenic layer and is interpreted as an isolated body of partial melt. The base of the seismogenic layer has a maximum depth of about 6.5 km beneath the spreading axis and deepens to about 7 km beneath a transform zone in the south of the area. Beneath the high-temperature part of the geothermal area, the maximum depth of earthquakes may be as shallow as 4 km. The geothermal gradient below drilling depths in various parts of the area ranges from 84 ± 9 °Ckm -1 within the low-temperature geothermal area of the transform zone to 138 ± 15 °Ckm -1 below the centre of the high-temperature geothermal area. Shallow maximum depths of earthquakes and therefore high average geothermal gradients tend to correlate with the intensity of the geothermal area and not with the location of the currently active spreading axis.

Effect of aging on the general corrosion and stress corrosion cracking of uranium--6 wt % niobium alloy

International Nuclear Information System (INIS)

Koger, J.W.; Ammons, A.M.; Ferguson, J.E.

1975-11-01

Mechanical properties of the uranium-6 wt percent niobium alloy change with aging time and temperature. In general, the ultimate tensile strength and hardness reach a peak, while elongation becomes a minimum at aging temperatures between 400 and 500 0 C. The first optical evidence of a second phase was in the 400 0 C-aged alloy, while complete transformation to a two-phase structure was seen in the 600 0 C-aged alloy. The maximum-strength conditions correlate with the minimum stress corrosion cracking (SCC) resistance. The maximum SCC resistance is found in the as-quenched and 150, 200, and 600 0 C-aged specimens. The as-quenched and 300 0 C-aged specimens had the greatest resistance to general corrosion in aqueous chloride solutions; the 600 0 C-aged specimen had the least resistance

Biomineral processing of high apatite containing low-grade indian uranium ore

International Nuclear Information System (INIS)

Abhilash; Mehta, K.D.; Pandey, B.D.; Ray, L.; Tamrakar, P.K.

2010-01-01

Microbial species isolated from source mine water, primarily an enriched culture of Acidithiobacillus ferrooxidans was employed for bio-leaching of uranium from a low-grade apatite rich uranium ore of Narwapahar Mines, India while varying pH, pulp density (PD), particle size, etc. The ore (0.047% U_3O_8), though of Singhbhum area (richest deposit of uranium ores in India), due to presence of some refractory minerals and high apatite (5%) causes a maximum 78% recovery through conventional processing. Bioleaching experiments were carried out by varying pH at 35"oC using 20%(w/v) PD and <76μm size particles resulting in 83.5% and 78% uranium bio-recovery at 1.7 and 2.0 pH in 40 days as against maximum recovery of 46% and 41% metal in control experiments respectively. Finer size (<45μm) ore fractions exhibited higher uranium dissolution (96%) in 40 days at 10% (w/v) pulp density (PD), 1.7 pH and 35"oC. On increasing the pulp density from 10% to 20% under the same conditions, the biorecovery of uranium fell down from 96% to 82%. The higher uranium dissolution during bioleaching at 1.7 pH with the fine size particles (<45μm) can be correlated with increase in redox potential from 598 mV to 708 mV and the corresponding variation of Fe(III) ion concentration in 40 days. (author)

Biomineral processing of high apatite containing low-grade indian uranium ore

Energy Technology Data Exchange (ETDEWEB)

Abhilash; Mehta, K.D.; Pandey, B.D., E-mail: biometnml@gmail.com [National Metallurgical Laboratory (CSIR), Jamshedpur (India); Ray, L. [Jadavpur Univ., FTBE Dept., Kolkata (India); Tamrakar, P.K. [Uranium Corp. of India Limited, CR& D Dept., Jaduguda (India)

2010-07-01

Microbial species isolated from source mine water, primarily an enriched culture of Acidithiobacillus ferrooxidans was employed for bio-leaching of uranium from a low-grade apatite rich uranium ore of Narwapahar Mines, India while varying pH, pulp density (PD), particle size, etc. The ore (0.047% U{sub 3}O{sub 8}), though of Singhbhum area (richest deposit of uranium ores in India), due to presence of some refractory minerals and high apatite (5%) causes a maximum 78% recovery through conventional processing. Bioleaching experiments were carried out by varying pH at 35{sup o}C using 20%(w/v) PD and <76μm size particles resulting in 83.5% and 78% uranium bio-recovery at 1.7 and 2.0 pH in 40 days as against maximum recovery of 46% and 41% metal in control experiments respectively. Finer size (<45μm) ore fractions exhibited higher uranium dissolution (96%) in 40 days at 10% (w/v) pulp density (PD), 1.7 pH and 35{sup o}C. On increasing the pulp density from 10% to 20% under the same conditions, the biorecovery of uranium fell down from 96% to 82%. The higher uranium dissolution during bioleaching at 1.7 pH with the fine size particles (<45μm) can be correlated with increase in redox potential from 598 mV to 708 mV and the corresponding variation of Fe(III) ion concentration in 40 days. (author)

Supercritical fluid extraction of uranium and thorium from nitric acid medium using organophosphorous compounds

Energy Technology Data Exchange (ETDEWEB)

Pitchaiah, K.C.; Sujatha, K.; Rao, C.V.S. Brahmmananda; Subramaniam, S.; Sivaraman, N.; Rao, P.R. Vasudeva [Indira Gandhi Centre for Atomic Research, Kalpakkam (India). Chemistry Group

2015-06-01

In recent years, Supercritical Fluid Extraction (SFE) technique has been widely used for the extraction of metal ions. In the present study, extraction of uranium from nitric acid medium was investigated using supercritical carbon dioxide (Sc-CO{sub 2}) containing various organophosphorous compounds such as trialkyl phosphates e.g. tri-iso-amyl phosphate (TiAP), tri-sec-butyl phosphate (TsBP) and tri-n-butyl phosphate (TBP), dialkylalkyl phosphonates, e.g. diamylamyl phosphonate (DAAP) and dibutyl butyl phosphonate (DBBP), dialkyl hydrogen phosphonates, e.g. dioctyl hydrogen phosphonate (DOHP), dioctylphosphineoxide (DOPO), trioctyl phosphine oxide (TOPO), n-octylphenyl N,N-diisobutyl carbamoylmethylphosphine oxide (CMPO) and di-2-ethyl-hexyl phosphoric acid (HDEHP). Some of these ligands have been investigated for the first time in the supercritical phase for the extraction of uranium. The extraction efficiency of uranium was studied with TiAP, DAAP and DBBP as a function of nitric acid concentration; the kinetics of the equilibration period (static extraction) and transportation of the metal complex (dynamic extraction) was investigated. The influence of pressure and temperature on the extraction behaviour of uranium with DAAP was studied from 4 N HNO{sub 3}. The extraction efficiency of uranium from 4 N nitric acid medium was found to increase in the order of phosphates < phosphonates < HDEHP < TOPO < CMPO. In the case of phosphates and phosphonates, the maximum extraction of uranium was found to be from 4 N HNO{sub 3} medium. The acidic extractants, HDEHP and DOHP showed relatively higher extraction at lower acidities. The relative extraction of uranium and thorium from their mixture was also examined using Sc-CO{sub 2} containing phosphates, phosphonates and TOPO. The ligand, TsBP provided better fractionation between uranium and thorium compared to trialkyl phosphates, dialkyl alkyl phosphonates and TOPO.

Chlorine-assisted leaching of Key Lake uranium ore

International Nuclear Information System (INIS)

Haque, K.E.

1981-04-01

Bench-scale chlorine-assisted leach tests were conducted on the Key Lake uranium ore. Leach tests conducted at 80 0 C on a slurry containing 50% solids during 10 hours of agitation gave the maximum extraction of uranium - 96% and radium-226 - 91%. Chlorine was added at 23.0 Kg Cl 2 /tonne of ore to maintain the leach slurry pH in the range of 1.5-1.0. To obtain residue almost free of radionuclides, hydrochloric acid leaches were conducted on the first stage leach residues. The second stage leach residue still was found to contain uranium - 0.0076% and radium-226 - 200 pCi/g of solids

Study on treatment of radioactive liquid waste from uranium ore processing by the use of nano Fe_3O_4 KT particles

International Nuclear Information System (INIS)

Vuong Huu Anh; Nguyen Ba Tien; Doan Thi Thu Hien; Luu Cao Nguyen; Nguyen Van Chinh

2015-01-01

Nano Fe_3O_4 KT was produced from the Military Institute of Science and Technology were used to adsorbed heavy metal elements in liquid waste. In this report, the nano Fe_3O_4 KT particles sized 80-100 nm and specific surface area was 50-70 m"2/g was applied to study the adsorption of radioactive elements in the liquid waste of uranium ores processing. The effective parameters on adsorption process included temperature, stirring rate, stirring time, the pH value of the solution, the initial concentration of uranium in solution. The results showed the maximum adsorption capacity of the nano Fe_3O_4 KT was 53.5 mg/g with conditions such as room temperature, stirring speed 120 rounds/minute, the pH value of solution was 8, stirring time about 2 hours (Uranium/materials). From the results obtained, nano Fe_3O_4 KT tested to treatment liquid waste of uranium ore processing after preliminary precipitation removed almost heavy metals and a part of radioactive elements. The results were analyzed on the ICP-MS and α, β total counting, instrument. The solution concentration after treatment was suitable for Vietnam discharge standards into environment (QCVN 40:2011 on Industrial wastewater). (author)

Behaviour of uranium under irradiation

International Nuclear Information System (INIS)

Adda, Y.; Mustelier, J.P.; Quere, Y.; Commissariat a l'Energie Atomique, Fontenay-aux-Roses

1964-01-01

The main results obtained in a study of the formation of defects caused in uranium by fission at low temperature are reported. By irradiation at 20 K. it was possible to determine the number of Frenkel pairs produced by one fission. An analysis of the curves giving the variations in electrical resistivity shows the size of the displacement spikes and the mechanism of defect creation due to fission. Irradiations at 77 K gave additional information, showing behaviour differences in the case of recrystallised and of cold worked uranium. The diffusion of rare gases was studied using metal-rare gas alloys obtained by electrical discharge, and samples of irradiated uranium. Simple diffusion is only responsible for the release of the rare gases under vacuum in cases where the rare gas content is very low (very slightly irradiated U). On the other hand when the concentration is higher (samples prepared by electrical discharge) the gas is given off by the formation, growth and coalescence of bubbles; the apparent diffusion coefficient is then quite different from the true coefficient and cannot be used in calculations on swelling. The various factors governing the phenomenon of simple diffusion were examined. It was shown in particular that a small addition of molybdenum could reduce the diffusion coefficient by a factor of 100. The precipitation of gas in uranium (Kr), in silver (Kr) and in Al-Li alloy (He) have been followed by measurement of the crystal parameter and of the electrical resistivity, and by electron microscope examination of thin films. The important part played by dislocations in the generation and growth of bubbles has been demonstrated, and it has been shown also that precipitation of bubbles on the dislocation lattice could block the development of recrystallisation. The results of these studies were compared with observations made on the swelling of uranium and uranium alloys U Mo and U Nb strongly irradiated between 400 and 700 C. In the case of Cubic

Uranium extraction from aqueous solution using dried and pyrolyzed tea and coffee wastes

International Nuclear Information System (INIS)

Zaynab Aly

2013-01-01

The adsorption of U(VI) onto dried and pyrolyzed tea and coffee wastes was investigated. The adsorption properties of the materials were characterized by measuring uranium uptake as a function of solution pH, kinetics and adsorption isotherms. pH profile of uranium adsorption where UO 2 2+ is expected to be the predominant species was measured between pH 0 and 4. Both Langmuir and Freundlich adsorption models were used to describe adsorption equilibria, and corresponding constants evaluated. Using the Langmuir model, the maximum adsorption capacity of uranium by dried tea and coffee wastes was 59.5 and 34.8 mg/g, respectively at 291 K. Adsorption thermodynamic constants, ΔHdeg ΔSdeg and ΔGdeg were also calculated from adsorption data obtained at three different temperatures. Adsorption thermodynamics of uranyl ions on dried tea and coffee systems indicated spontaneous and endothermic processes. Additionally, a Lagergren pseudo-second-order kinetic model was used to fit the kinetic experimental data for both adsorbents and the constants evaluated. Dried tea and coffee wastes proved to be effective adsorbents with high capacities and significant advantage of a very low cost. (author)

The solubility of uranium in cementitious near-field chemical conditions

Energy Technology Data Exchange (ETDEWEB)

Baston, G.M.N.; Brownsword, M.; Cross, J.E.; Hobley, J.; Moreton, A.D.; Smith-Briggs, J.L.; Thomason, H.P. [AEA Decommissioning and Waste Management, Harwell (United Kingdom)

1993-05-01

Tetravalent and hexavalent uranium solubilities have been measured in cement-equilibriated water for pH values from 4 to 13. Tetravalent uranium solubilities at pH 12 have been measured by three experimental techniques: oversaturation, undersaturation and by the use of an electrochemical cell which controlled the redox conditions. The experimentally obtained data have been simulated using the thermodynamic equilibrium program HARPHRQ in conjunction with three different sets of thermodynamic data for uranium. In each case, differences were found between the predicted and measured uranium behaviour. For hexavalent uranium at high pH values the model suggested the formation of anionic hydrolysis products which led to the prediction of uranium solubilities significantly higher than those observed. Refinement of the thermodynamic data used in the model enabled the derivation of maximum values for the formation constants of these species under cementitious conditions. Similarly, the experimental data have been used to refine a model of tetravalent uranium solubility under cementitious near-field conditions. (author).

The solubility of uranium in cementitious near-field chemical conditions

International Nuclear Information System (INIS)

Baston, G.M.N.; Brownsword, M.; Cross, J.E.; Hobley, J.; Moreton, A.D.; Smith-Briggs, J.L.; Thomason, H.P.

1993-05-01

Tetravalent and hexavalent uranium solubilities have been measured in cement-equilibriated water for pH values from 4 to 13. Tetravalent uranium solubilities at pH 12 have been measured by three experimental techniques: oversaturation, undersaturation and by the use of an electrochemical cell which controlled the redox conditions. The experimentally obtained data have been simulated using the thermodynamic equilibrium program HARPHRQ in conjunction with three different sets of thermodynamic data for uranium. In each case, differences were found between the predicted and measured uranium behaviour. For hexavalent uranium at high pH values the model suggested the formation of anionic hydrolysis products which led to the prediction of uranium solubilities significantly higher than those observed. Refinement of the thermodynamic data used in the model enabled the derivation of maximum values for the formation constants of these species under cementitious conditions. Similarly, the experimental data have been used to refine a model of tetravalent uranium solubility under cementitious near-field conditions. (author)

Verification of surface minimum, mean, and maximum temperature forecasts in Calabria for summer 2008

Directory of Open Access Journals (Sweden)

S. Federico

2011-02-01

Full Text Available Since 2005, one-hour temperature forecasts for the Calabria region (southern Italy, modelled by the Regional Atmospheric Modeling System (RAMS, have been issued by CRATI/ISAC-CNR (Consortium for Research and Application of Innovative Technologies/Institute for Atmospheric and Climate Sciences of the National Research Council and are available online at http://meteo.crati.it/previsioni.html (every six hours. Beginning in June 2008, the horizontal resolution was enhanced to 2.5 km. In the present paper, forecast skill and accuracy are evaluated out to four days for the 2008 summer season (from 6 June to 30 September, 112 runs. For this purpose, gridded high horizontal resolution forecasts of minimum, mean, and maximum temperatures are evaluated against gridded analyses at the same horizontal resolution (2.5 km.

Gridded analysis is based on Optimal Interpolation (OI and uses the RAMS first-day temperature forecast as the background field. Observations from 87 thermometers are used in the analysis system. The analysis error is introduced to quantify the effect of using the RAMS first-day forecast as the background field in the OI analyses and to define the forecast error unambiguously, while spatial interpolation (SI analysis is considered to quantify the statistics' sensitivity to the verifying analysis and to show the quality of the OI analyses for different background fields.

Two case studies, the first one with a low (less than the 10th percentile root mean square error (RMSE in the OI analysis, the second with the largest RMSE of the whole period in the OI analysis, are discussed to show the forecast performance under two different conditions. Cumulative statistics are used to quantify forecast errors out to four days. Results show that maximum temperature has the largest RMSE, while minimum and mean temperature errors are similar. For the period considered

Role of Some Isolated Fungi in The Biological Leaching of Uranium From Low Grade Cretaceous Sandstone

International Nuclear Information System (INIS)

Ibrahim, H.A.; Morsy, A.; El-Sheikh, E.M.

2012-01-01

Microbiological leaching has been used as an alternative approach to conventional hydrometallurgical methods of uranium extraction. In this investigation, the biological leaching of uranium by isolated fungi from low grade sandstone was studied. Five isolates of fungi were obtained from sandstone sample. Cladosporium oxysporum and Penicilluim stoloniferum exhibited high potential in generating a variety of organic acids effective for uranium extraction. The percentages of organic acid produced by fungi were determined. By-product such as molasses was tested. The maximum dissolution of uranium was achieved at the following conditions; incubation period 6 days, pulp density 1:3 g/L, ph 3.5 and at 30 degree C. Maximum solubilization of uranium with values of 54% and 67% were achieved by Cladosporium oxysporum and Penicilluim stoloniferum, respectively. From properly prepared pregnant bio-leach liquor, the leached uranium was recovered in the form of marketable products (3UO 3 NH 3 .5H 2 O) using classical chemical technique and the product was confirmed using XRD techniques

Development of sorbers for the recovery of uranium from seawater. Part 2. The accumulation of uranium from seawater by resins containing amidoxime and imidoxime functional groups

International Nuclear Information System (INIS)

Astheimer, L.; Schenk, H.J.; Witte, E.G.; Schwochau, K.

1983-01-01

Hydroxylamine derivatives of cross-linked poly(acrylonitriles), so-called poly(acrylamidoxime) resins, are suitable for the accumulation of uranium from natural seawater of pH = 8.1 to 8.3. Depending on the method of manufacture, these sorbers yield excellent uranium loadings up to some thousand ppM which roughly equals the average uranium content of actually explored uranium ores. The rate of uranium uptake, which is 5 to 30 ppM/d at room temperature, increases with increasing temperature of seawater. Uranium can be eluted by 1 M HCl with an elution efficiency of more than 90%. Owing to a certain instability of the uranium binding groups in acid eluants, the uranium uptake decreases with increasing number of sorption-elution cycles. Hydroxylamine derivatives of poly(acrylonitrile) are shown to contain simultaneously at least two kinds of functional groups: open-chain amidoxime groups which are stable and cyclic imidoxime groups which are unstable in 1 M HCl. Experimental evidence is presented that the uptake of uranium from natural seawater is closely related to the presence of cyclic imidoxime configurations in the polyacrylic lattice. Polystyrene and poly(glycidylmethacrylate)-based amidoxime and imide dioxime resins are less effective in extracting uranium from natural seawater. 10 figures, 4 tables

Study of the temperature influence during the uranium (Vi) sorption on surface of ZrP2O7 in presence of oxalic and salicylic acid

International Nuclear Information System (INIS)

Garcia G, N.

2013-01-01

This work studies the effect of temperature on the uranium (Vi) sorption onto zirconium diphosphate in the presence of organic acids (oxalic and salicylic acids). Zirconium diphosphate was synthesized by a chemical condensation reaction and characterized using several analytical techniques, in order to check its purity. This point is very important because the presence of any impurities or secondary phases may interfere with the hydration and sorption process. Prior to the sorption experiments, three batches of zirconium diphosphate were pre-equilibrated with NaClO 4 , oxalic acid or salicylic acid solutions. The hydrated solids were washed and dried and then again characterized in order to study the interactions between organic acids and zirconium diphosphate surface. Uranium sorption onto zirconium diphosphate (pre-equilibrated with NaClO 4 , oxalic acid and salicylic acid solutions) was investigated as a function of ph, organic acid and temperature (20, 40 y 60 grades C). Thermodynamic parameters for the sorption reactions (enthalpy change, entropy change and Gibbs free energy change) were determined from temperature dependence of distribution coefficient by using the Vant Hoff equation. Solids characterization after hydration shows that exist an interaction between organic acids and ZrP 2 O 7 . This fact was confirmed with the microcalorimetry study, the reaction heat for hydration of zirconium diphosphate in NaClO 4 solution was exothermic (-269.59 mJ) and for hydration of zirconium diphosphate in oxalic acid solution was endothermic (53.64 mJ). The experimental results showed important differences in the sorption mechanisms for the reaction of Uranium with ZrP 2 O 7 in the presence and absence of organic acids. For the zirconium diphosphate hydrated with oxalic acid, the sorption percentage was 50% from lowest ph values. For the zirconium diphosphate hydrated with salicylic acid, the initial concentration of uranium was 6 x 10 -4 M and a percentage of 10% was

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.)

Magnesium and uranium ignition in different gaseous atmospheres

International Nuclear Information System (INIS)

Darras, R.; Baque, P.; Leclercq, D.

1960-01-01

Magnesium, uranium and some of their alloys burning temperatures have been systematically determined in an air or carbon dioxide atmosphere, either dry or wet. Two different ways of heating have been used: either continuously rising up the temperature, or heating to and then maintaining a constant temperature. The results are clearly different in the two cases. Besides, if moisture has little effect on the magnesium burning temperatures in air, it does lower them by about 130-140 deg. C in CO 2 . The differences of sight between the burning of magnesium and uranium have been noticed; this leads to distinguish between an 'ignition' and an 'inflammation'. (author) [fr

Tectonics, hydrothermal zoning, and uranium in the central Andes

Energy Technology Data Exchange (ETDEWEB)

Gabelman, J W

1961-01-01

The geological features of the Peruvian Andes are discussed in some detail. The geologic history of the Andrean tectonics was found to be virtually the same as that represented in both North and South American Cordillera. The study indicated that Andrean hydrothermal mineralization occurred intermittently but in close time relation with accompanying deformations from the late Cretaceous or early Tertiary up to the present. The mineralization cycle is discussed as it relates to several metals, particularly uranium. Uranium is believed to occupy the same several temperature--environmental positions in the Andes that it does throughout the rest of the western hemisphere Cordillera. Even though uranium is present in minor quantities in several high-to-moderate-temperature environments, the bulk of uranium present in the cycle is believed to precipitate in the subepithermal environment.

Thermal conductivity of uranium: effects of purity and microstructure

International Nuclear Information System (INIS)

Sandenaw, T.A.

1975-10-01

Thermal conductivity curves for polycrystalline uranium are presented for the temperature range below 373 0 K. The curves are for specimens prepared by different fabrication procedures from material of known purity and hardness. Included is a curve for U/2wt percent Mo alloy. Different mechanisms appear to be influencing the thermal conductivity behavior of uranium in well-defined temperature regions: below 37 to 43 0 K, approximately 40 to approximately 80 0 K, 80 to approximately 280 0 K, and from 280 0 K to the α → β transformation temperature. Mechanisms responsible for results in one temperature region continue to exert a strong influence in the next higher temperature region. Impurities and initial microstructure seem to influence results at any starting temperature. Evidence is presented for the possibility of imperfection ordering in uranium between approximately 40 and approximately 280 0 K. It is postulated that the type of ordering is capable with a martensite-like behavior and that all physical property results depend on the extent of a modification of the α-phase on cooling below approximately 280 0 K

The maximum temperature of a thermodynamic cycle effect on weight-dimensional characteristics of the NPP energy blocks with air cooling

International Nuclear Information System (INIS)

Bezborodov, Yu.A.; Bubnov, V.P.; Nesterenko, V.B.

1982-01-01

The cycle maximum temperature effect on the properties of individual apparatuses and total NPP energy blocks characteristics has been investigated. Air, nitrogen, helium and chemically reacting system N 2 O 4 +2NO+O 2 have been considered as coolants. The conducted investigations have shown that maximum temperature of thermodynamical cycle affects considerably both the weight-dimensional characteristics of individual elements of NPP and total characteristics of NPP energy block. Energy blocks of NPP with air cooling wherein dissociating nitrogen tetroxide is used as working body, have better indexes on the majority of characteristics in comparison with blocks with air, nitrogen and helium cooling. If technical restrictions are to be taken into account (thermal resistance of metals, coolant decomposition under high temperatures, etc.) then dissociating nitrogen tetroxide should be recommended as working body and maximum cycle temperature in the range from 500 up to 600 deg C

METHOD OF PRODUCING URANIUM METAL BY ELECTROLYSIS

Science.gov (United States)

Piper, R.D.

1962-09-01

A process is given for making uranium metal from oxidic material by electrolytic deposition on the cathode. The oxidic material admixed with two moles of carbon per one mole of uranium dioxide forms the anode, and the electrolyte is a mixture of from 40 to 75% of calcium fluoride or barium fluoride, 15 to 45% of uranium tetrafluoride, and from 10 to 20% of lithium fluoride or magnesium fluoride; the temperature of the electrolyte is between 1150 and 1175 deg C. (AEC)

Study on treatment of radioactive liquid waste from uranium ore processing by the use of nano oxide ferromagnetic

International Nuclear Information System (INIS)

Vuong Huu Anh; Nguyen Van Chinh; Nguyen Ba Tien; Doan Thi Thu Hien; Luu Cao Nguyen

2015-01-01

Nano oxide ferromagnetic Fe_3O_4 KT which was produced by the Military Institute of Science and Technology were used to adsorbed heavy metal elements in liquid waste. In this report, the nano oxide ferromagnetic Fe_3O_4 KT with the particle size of 80-100 nm and the specific surface area of 50-70 m"2/g was applied to study the adsorption of radioactive elements in the liquid waste of uranium ores processing. The effective parameters on adsorption process included temperature, stirring rate, stirring time, the pH value of the solution, the initial concentration of uranium in solution were investigated. The results showed that the maximum adsorption capacity for uranium of the nano Fe_3O_4 KT was 53.5 mgU/g with conditions such as: room temperature, stirring speed 120 rounds/minute, the pH value of solution was 8, stirring time about 2 hours . From the results obtained, nano Fe_3O_4 KT was tested to treatment real liquid waste of uranium ore processing after removing almost heavy metals and a part of radioactive elements by preliminary precipitation at pH 8. The results were analyzed on the ICP-MS and α, β total activity equipment, the solution concentration after treatment suitable for Vietnamese Technical Regulation on industrial wastewater QCVN 40: 2011 (concentrations of heavy metals; total activity of α and β). (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)

Liquid membranes and process for uranium recovery therewith

International Nuclear Information System (INIS)

Frankenfeld, J.W.; Li, N.N.T.; Bruncati, R.L.

1981-01-01

A liquid membrane system consisting of water-in-oil type emulsions dispersed in water, which is capable of extracting uranium-containing ions from an aqueous feed solution containing uranium ions at a temperature in the range of 25 0 C to 80 0 C, is described. The emulsion comprises an aqueous interior phase surrounded by a surfactant-containing exterior phase. The exterior phase is immiscible with the interior phase and comprises a transfer agent capable of transporting selectively the desired uranium-containing ions and a solvent for the transfer agent. The interior phase comprises a reactant capable of removing uranium-containing ions from the transfer agent and capable of changing the valency of the uranium in uranium-containing ions to a second valency state and converting the uranium-containing ions into a nonpermeable form. (U.K.)

Thermodynamics of the vaporization of uranium tetrabromide

International Nuclear Information System (INIS)

Singh, Z.; Prasad, R.; Venugopal, P.V.; Roy, K.N.; Sood, D.D.

1981-01-01

Vapour pressures of solid and liquid uranium tetrabromide have been measured in the temperature range of 696 to 805 K and 805 to 1003 K respectively by transpiration and evaporation-temperature techniques. The vapour pressures obtained by the two techniques are in good agreement and have been combined to give the reported vapour-pressure equations for solid and liquid uranium tetrabromide. The melting temperature, the normal boiling temperature, the standard enthalpy of vaporization ΔH 0 (vap, 298.15 K), and the standard entropy of vaporization ΔS 0 (vap, 298.15 K) are reported. The enthalpy of fusion ΔH 0 (fus, 802 K) is also reported. The thermodynamic quantities from the present study are compared with those in the literature and critically analysed. (author)

Uncertainty hovers over the uranium market

International Nuclear Information System (INIS)

Holtorp, J.

1981-01-01

The results of evaluation of capitalist countries requirements for uranium for nuclear power engineering in 1985-1995 are presented. The data of maximum and minimum forecasting of NPP construction have been taken into account. It is assumed that the NPP total power in capitalist countries is to attain by 1990 335-350 million kW and by 1995 356-549 million kW. It is pointed out that by 1990 uranium production will constitute 82 thousand a year: 45% of this amount will be produced at existing mines, 17% at mines under construction and 38% at the designed mines. Use of only operating mines will enable in 1985 to have reserves of produced uranium sufficient for meeting the requirements of nuclear power engineering during 2.2 years and in 1990 - 0.7 year. On the basis of analysis of the given data the conclusion is drawn that uranium requirements in the nearest future will not be great, particularly if the observed decrease in the NPPs construction scale growth rate is preserved [ru

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

New England observed and predicted August stream/river temperature maximum positive daily rate of change points

Data.gov (United States)

U.S. Environmental Protection Agency — The shapefile contains points with associated observed and predicted August stream/river temperature maximum positive daily rate of change in New England based on a...

New England observed and predicted July stream/river temperature maximum positive daily rate of change points

Data.gov (United States)

U.S. Environmental Protection Agency — The shapefile contains points with associated observed and predicted July stream/river temperature maximum positive daily rate of change in New England based on a...

New England observed and predicted July maximum negative stream/river temperature daily rate of change points

Data.gov (United States)

U.S. Environmental Protection Agency — The shapefile contains points with associated observed and predicted July stream/river temperature maximum negative daily rate of change in New England based on a...

Study on thermo-oxide layers of uranium-niobium alloy

International Nuclear Information System (INIS)

Luo Lizhu; Yang Jiangrong; Zhou Ping

2010-01-01

Surface oxides structure of uranium-niobium alloys which were annealed under different temperatures (room temperature, 100, 200, 300 degree C, respectively)in air were studied by X-ray photoelectron spectroscopy (XPS) analysis and depth profile. Thickness of thermo-oxide layers enhance with the increasing oxide temperature, and obvious changes to oxides structure are observed. Under different delt temperatures, Nb 2 O 5 are detected on the initial surface of U-Nb alloys, and a layer of NbO mixed with some NbO x (0 2 O 5 and Nb metal. Dealing samples in air from room temperature to 200 degree C, non-stoichiometric UO 2+x (UO 2 + interstitial oxygen, P-type semiconductor) are found on initial surface of U-Nb alloys, which has 0.7 eV shift to lower binding energy of U 4f 7/2 characteristics comparing to that of UO 2 . Under room temperature, UO 2 are commonly detected in the oxides layer, while under temperature of 100 and 200 degree C, some P-type UO 2+x are found in the oxide layers,which has a satellite at binding energy of 396.6 eV. When annealing at 300 degree C, higher valence oxides, such as U 3 O 8 or UO x (2 5/2 and U 4f 7/2 peaks are 392.2 and 381.8 eV, respectively. UO 2 mixed uranium metal are the main compositions in the oxide layers. From the results, influence of temperature to oxidation of uranium is more visible than to niobium in uranium-niobium alloys. (authors)

Extractive spectrophotometric determination of uranium with malachite green

International Nuclear Information System (INIS)

Dubey, S.C.; Nadkarni, M.N.

1977-01-01

A sensitive spectrophotometric method based on the extraction of a uranium-benzoate-Malachite Green complex by chlorobenzene is described. The absorption maximum is at 635 nm and the molar absorptivity is 8.3 x 10 4 1. mole -1 cm -1 . A preliminary separation of uranium by extraction with methyl isobutyl ketone from acid-deficient aluminium nitrate solution is used to avoid interferences. An aliquot of the extract in then diluted with chlorobenzene and shaken with benzoate buffer containing Malachite Green (MG). The method has been applied for the determination of uranium in a synthetic leach solution. The complex extracted is probably [U0 2 (C 6 H 5 C00 3 - ][MG + ]. (author)

Dynamic Performance of Maximum Power Point Trackers in TEG Systems Under Rapidly Changing Temperature Conditions

Science.gov (United States)

Man, E. A.; Sera, D.; Mathe, L.; Schaltz, E.; Rosendahl, L.

2016-03-01

Characterization of thermoelectric generators (TEG) is widely discussed and equipment has been built that can perform such analysis. One method is often used to perform such characterization: constant temperature with variable thermal power input. Maximum power point tracking (MPPT) methods for TEG systems are mostly tested under steady-state conditions for different constant input temperatures. However, for most TEG applications, the input temperature gradient changes, exposing the MPPT to variable tracking conditions. An example is the exhaust pipe on hybrid vehicles, for which, because of the intermittent operation of the internal combustion engine, the TEG and its MPPT controller are exposed to a cyclic temperature profile. Furthermore, there are no guidelines on how fast the MPPT must be under such dynamic conditions. In the work discussed in this paper, temperature gradients for TEG integrated in several applications were evaluated; the results showed temperature variation up to 5°C/s for TEG systems. Electrical characterization of a calcium-manganese oxide TEG was performed at steady-state for different input temperatures and a maximum temperature of 401°C. By using electrical data from characterization of the oxide module, a solar array simulator was emulated to perform as a TEG. A trapezoidal temperature profile with different gradients was used on the TEG simulator to evaluate the dynamic MPPT efficiency. It is known that the perturb and observe (P&O) algorithm may have difficulty accurately tracking under rapidly changing conditions. To solve this problem, a compromise must be found between the magnitude of the increment and the sampling frequency of the control algorithm. The standard P&O performance was evaluated experimentally by using different temperature gradients for different MPPT sampling frequencies, and efficiency values are provided for all cases. The results showed that a tracking speed of 2.5 Hz can be successfully implemented on a TEG

Maximum surface level and temperature histories for Hanford waste tanks

International Nuclear Information System (INIS)

Flanagan, B.D.; Ha, N.D.; Huisingh, J.S.

1994-01-01

Radioactive defense waste resulting from the chemical processing of spent nuclear fuel has been accumulating at the Hanford Site since 1944. This waste is stored in underground waste-storage tanks. The Hanford Site Tank Farm Facilities Interim Safety Basis (ISB) provides a ready reference to the safety envelope for applicable tank farm facilities and installations. During preparation of the ISB, tank structural integrity concerns were identified as a key element in defining the safety envelope. These concerns, along with several deficiencies in the technical bases associated with the structural integrity issues and the corresponding operational limits/controls specified for conduct of normal tank farm operations are documented in the ISB. Consequently, a plan was initiated to upgrade the safety envelope technical bases by conducting Accelerated Safety Analyses-Phase 1 (ASA-Phase 1) sensitivity studies and additional structural evaluations. The purpose of this report is to facilitate the ASA-Phase 1 studies and future analyses of the single-shell tanks (SSTs) and double-shell tanks (DSTs) by compiling a quantitative summary of some of the past operating conditions the tanks have experienced during their existence. This report documents the available summaries of recorded maximum surface levels and maximum waste temperatures and references other sources for more specific data

Investigation of uranium plasma emission from 1050 to 6000 A

International Nuclear Information System (INIS)

Mack, J.M. Jr.

1977-12-01

Absolute emission coefficient measurements on arc-generated uranium plasmas in local thermodynamic equilibrium are described for a wavelength bandwidth of 1050 to 6000A. Low- and high-pressure arcs were investigated for their emission properties, characteristic temperatures and uranium partial pressures. Temperatures from 5500 to 8000 K and uranium partial pressures from 0.001 to 0.01 atm were found at the arc centerline. The new emission data are compared with other similar experimental results and to existing theoretical calculations. The effects of cold-layer UF 6 photoabsorption on uranium plasma emission characteristics are established for UF 6 molecular densities ranging from 1.0 x 10 16 to 1.0 x 10 17 cm -3 and layer thickness from 1.0 to 5.0 cm

Depleted uranium hexafluoride: Waste or resource?

International Nuclear Information System (INIS)

Schwertz, N.; Zoller, J.; Rosen, R.; Patton, S.; Bradley, C.; Murray, A.

1995-07-01

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

Study of the recrystallisation of irradiated uranium

International Nuclear Information System (INIS)

Bloch, J.; Mustelier, J.P.; Bussy, P.; Blin, J.

1958-01-01

1- Study of the recrystallisation of irradiated uranium. The recrystallisation of uranium irradiated to a burnup level of 220 MWj/t, at a temperature of the order of 350 deg. C, has been investigated. The observations were made chiefly by means of micrography an hardness measurements. If the irradiated metal is compared with a cold-drawn metal showing the same shearing of the twinned crystals, and therefore the same rate of plastic deformation, as the irradiated metal, it is noted that the restoring of the irradiated metal takes place at a considerably higher temperature than that of the cold-drawn metal. Pre-crystallisation is very much delayed. Only, a passage of the α-β transformation point quickly wipes out irradiation effect. 2- Hardening of uranium by irradiation. Using hardness measurements we have studied more especially the effect of very weak irradiations on uranium (integrated flux 16 nvt). The hardness does not increase linearly with the flux, but a period of incubation is observed probably representing the time necessary for saturation of the dislocations. (author) [fr

Uranium redox transition pathways in acetate-amended sediments

Science.gov (United States)

Bargar, John R.; Williams, Kenneth H.; Campbell, Kate M.; Long, Philip E.; Stubbs, Joanne E.; Suvorova, Elenal I.; Lezama-Pacheco, Juan S.; Alessi, Daniel S.; Stylo, Malgorzata; Webb, Samuel M.; Davis, James A.; Giammar, Daniel E.; Blue, Lisa Y.; Bernier-Latmani, Rizlan

2013-01-01

Redox transitions of uranium [from U(VI) to U(IV)] in low-temperature sediments govern the mobility of uranium in the environment and the accumulation of uranium in ore bodies, and inform our understanding of Earth’s geochemical history. The molecular-scale mechanistic pathways of these transitions determine the U(IV) products formed, thus influencing uranium isotope fractionation, reoxidation, and transport in sediments. Studies that improve our understanding of these pathways have the potential to substantially advance process understanding across a number of earth sciences disciplines. Detailed mechanistic information regarding uranium redox transitions in field sediments is largely nonexistent, owing to the difficulty of directly observing molecular-scale processes in the subsurface and the compositional/physical complexity of subsurface systems. Here, we present results from an in situ study of uranium redox transitions occurring in aquifer sediments under sulfate-reducing conditions. Based on molecular-scale spectroscopic, pore-scale geochemical, and macroscale aqueous evidence, we propose a biotic–abiotic transition pathway in which biomass-hosted mackinawite (FeS) is an electron source to reduce U(VI) to U(IV), which subsequently reacts with biomass to produce monomeric U(IV) species. A species resembling nanoscale uraninite is also present, implying the operation of at least two redox transition pathways. The presence of multiple pathways in low-temperature sediments unifies apparently contrasting prior observations and helps to explain sustained uranium reduction under disparate biogeochemical conditions. These findings have direct implications for our understanding of uranium bioremediation, ore formation, and global geochemical processes.

The use of carbonate lixiviants to remove uranium from uranium-contaminated soils

International Nuclear Information System (INIS)

Francis, C.W.; Lee, S.Y.; Wilson, J.H.; Timpson, M.E.; Elless, M.P.

1997-01-01

The objective of this research was to design an extraction media and procedure that would selectively remove uranium without adversely affecting the soils' physicochemical characteristics or generating secondary waste forms difficult to manage or dispose of. Investigations centered around determining the best lixivant and how the various factors such as pH, time, and temperature influenced extraction efficiency. Other factors investigated included the influence of attrition scrubbing, the effect of oxidants and reductants and the recycling of lixiviants. Experimental data obtained at the bench- and pilot-scale levels indicated 80 to 95% of the uranium could be removed from the uranium-contaminated soils by using a carbonate lixiviant. The best treatment was three successive extractions with 0.25 M carbonate-bicarbonate (in presence of KMnO 4 as an oxidant) at 40 C followed with two water rinses

Adsorption of uranium(VI) from sulphate solutions using Amberlite IRA-402 resin: Equilibrium, kinetics and thermodynamics study

International Nuclear Information System (INIS)

Solgy, Mostafa; Taghizadeh, Majid; Ghoddocynejad, Davood

2015-01-01

Highlights: • Adsorption of uranium from sulphate solutions by an anion exchange resin. • The effects of pH, contact time and adsorbent dosage were investigated. • The adsorption equilibrium is well described by the Freundlich isotherm model. • The adsorption kinetics can be predicted by the pseudo second-order model. • The adsorption is a physical, spontaneous and endothermic process. - Abstract: In the present study, adsorption of uranium from sulphate solutions was evaluated using Amberlite IRA-402 resin. The variation of adsorption process was investigated in batch sorption mode. The parameters studied were pH, contact time and adsorbent dosage. Langmuir and Freundlich isotherm models were used in order to present a mathematical description of the equilibrium data at three different temperatures (25 °C, 35 °C and 45 °C). The final results confirmed that the equilibrium data tend to follow Freundlich isotherm model. The maximum adsorption capacity of Amberlite IRA-402 for uranium(VI) was evaluated to be 213 mg/g for the Langmuir model at 25 °C. The adsorption of uranium on the mentioned anion exchange resin was found to follow the pseudo-second order kinetic model, indicating that chemical adsorption was the rate limiting-step. The values of thermodynamic parameters proved that adsorption process of uranium onto Amberlite IRA-402 resin could be considered endothermic (ΔH > 0) and spontaneous (ΔG < 0)

Selective leaching of uranium from uranium-contaminated soils: Progress report 1

International Nuclear Information System (INIS)

Francis, C.W.; Mattus, A.J.; Farr, L.L.; Elless, M.P.; Lee, S.Y.

1993-02-01

Three soils and a sediment contaminated with uranium were used to determine the effectiveness of sodium carbonate and citric acid leaching to decontaminated or remove uranium to acceptable regulatory levels. Two of the soils were surface soils from the DOE facility formerly called the Feed Materials Production Center (FMPC) at Fernald, Ohio. This facility is presently called the Femald Environmental Management Project (FEMP). Carbonate extractions generally removed from 70 to 90% of the uranium from the Fernald storage pad soil. Uranium was slightly more difficult to extract from the Fernald incinerator and the Y-12 landfarm soils. Very small amounts of uranium could be extracted from the storm sewer sediment. Extraction with carbonate at high solution-to-soil ratios were as effective as extractions at low solution-to-soil ratios, indicating attrition by the paddle mixer was not significantly different than that provided in a rotary extractor. Also, pretreatments such as milling or pulverizing the soil sample did not appear to increase extraction efficiency when carbonate extractions were carried out at elevated temperatures (60 degree C) or long extraction times (23 h). Adding KMnO 4 in the carbonate extraction appeared to increase extraction efficiency from the Fernald incinerator soil but not the Fernald storage pad soil. The most effective leaching rates (> 90 % from both Fernald soils) were obtained using a citrate/dithionite extraction procedure designed to remove amorphous (noncrystalline) iron/aluminum sesquioxides from surfaces of clay minerals. Citric acid also proved to be a very good extractant for uranium

Experimental leaching of uranium from tuffaceous rocks

International Nuclear Information System (INIS)

Goodell, P.C.; Trentham, R.C.

1980-07-01

The premise to be tested in this work is that felsic volcanic rocks particularly ash-flow tuffs, can serve as source rocks for certain uranium deposits. The applicability of this idea to several geologic environments is investigated. A genetic model is developed dealing with the behavior of uranium during and subsequent to ash-flow tuff deposition. It is based upon previously described investigations, geologic logic, data presented here, and speculation. Ash-flow tuff sequences described in the literature show significant alkali element variation, particularly in thick tuff units. Some variation is attributed to initial magma variations, whereas additional change may be produced during cooling and degassing of the tuff. Uranium variations have been documented in tuff sequences which are assumed to represent magmatic compositions. Uranium may be released during the initial degassing, during hydrothermal alteration, and/or during later diagenesis. Experimental studies have been designed and carried out to simulate natural leaching conditions such as might occur during diagenesis. Synthetic ground waters have been pumped through pulverized uraniferous vitrophyres. Major and minor element contents have been determined. The most significant chemical changes take place quickly, within a matter of days. Several starting and product leachant solutions were analyzed fluorimetrically for uranium. They show significant increases in uranium contents, from less than 1 ppB at the start to greater than 10 ppB maximu. Such leachant solutions might be significant transport agents of uranium given geologic time. Leaching at low temperatures appears to involve a thin surface reaction and diffusion layer. Both dissolution and ion exchange influence the leachant composition. It is also concluded that glassy ash-flow tuffs may serve as uranium source rocks during low temperature diagenetic changes

Global view of F-region electron density and temperature at solar maximum

International Nuclear Information System (INIS)

Brace, L.H.; Theis, R.F.; Hoegy, W.R.

1982-01-01

Dynamics Explorer-2 is permitting the first measurements of the global structure of the F-regions at very high levels of solar activity (S>200). Selected full orbits of Langmuir probe measurements of electron temperature, T/sub e/, and density, N/sub e/, are shown to illustrate this global structure and some of the ionospheric features that are the topic of other papers in this issue. The ionospheric thermal structure is of particular interest because T/sub e/ is a sensitive indicator of the coupling of magnetospheric energy into the upper atmosphere. A comparison of these heating effects with those observed at solar minimum shows that the magnetospheric sources are more important at solar maximum, as might have been expected. Heating at the cusp, the auroral oval and the plasma-pause is generally both greater and more variable. Electron cooling rate calculations employing low latitude measurements indicate that solar extreme ultraviolet heating of the F region at solar maximum is enhanced by a factor that is greater than the increase in solar flux. Some of this enhanced electron heating arises from the increase in electron heating efficiency at the higher N/sub e/ of solar maximum, but this appears insufficient to completely resolve the discrepancy

Uranium dioxide calcining apparatus and method

International Nuclear Information System (INIS)

Cole, E.A.; Peterson, R.S.

1978-01-01

This invention relates to an improved continuous calcining apparatus for consistently and controllably producing from calcinable reactive solid compounds of uranium, such as ammonium diuranate, uranium dioxide (UO 2 ) having an oxygen to uranium ratio of less than 2.2. The apparatus comprises means at the outlet end of a calciner kiln for receiving hot UO 2 , means for cooling the UO 2 to a temperature of below 100 0 C and conveying the cooled UO 2 to storage or to subsequent UO 2 processing apparatus where it finally comes into contact with air, the means for receiving, cooling and conveying being sealed to the outlet end of the calciner and being maintained full of UO 2 and so operable as to exclude atmospheric oxygen from coming into contact with any UO 2 which is at elevated temperatures where it would readily oxidize, without the use of extra hydrogen gas in said means

Contribution to the study of the uranium-hydrogen system; Contribution a l'etude du systeme uranium-hydrogene

Energy Technology Data Exchange (ETDEWEB)

Chevallier, J [Commissariat a l' Energie Atomique, Grenoble (France). Centre d' Etudes Nucleaires

1965-01-01

Previous work on uranium-hydrogen system is reviewed. The U-H{sub 2}-UH{sub n} equilibrium is then investigated at pressures below one atmosphere, i.e. at temperatures lower than 430 deg. C. The hydride obtained at equilibrium is deficient in hydrogen (UH{sub n<3}), the hydrogen deficit increasing as the temperature rises. Thermodynamic functions for the formation of non-stoichiometric hydride and of one hydrogen vacancy are derived from pressure composition isotherms, in U-H phase diagram is proposed. The hydrogenation of U-UC alloys is also examined at pressures below one atmosphere with regard to the equilibrium: (free U + UC) - H{sub 2}-UH{sub n}. The equilibrium conditions are found different from that observed for pure uranium. (author) [French] Une etude bibliographique du systeme uranium-hydrogene est exposee. L'equilibre U-H{sub 2}-UH{sub n} est ensuite etudie sous des pressions inferieures a une atmosphere, soit aux temperatures inferieures a environ 430 degs. C. L'hydrure obtenu a l'equilibre est deficitaire en hydrogene - UH{sub n<3} - et d'autant plus que la temperature s'eleve. Les grandeurs thermodynamiques relatives a la formation et a la saturation de l'hydrure, ainsi qu'a la formation d'une lacune d'hydrogene sont deduites des pressions d'equilibre. Un modele de diagramme de phases U-H est propose. L'hyduration des alliages U-UC est etudiee egalement sous des pressions inferieures a l'atmosphere, au point de vue de l'equilibre (U libre + UC) - H{sub 2}-UH{sub n}. Les conditions d'equilibre sont trouvees differentes de celles observees sur l'uranium pur. (auteur)

Uranium

International Nuclear Information System (INIS)

Hamdoun, N.A.

2007-01-01

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

X-ray photoelectron and Auger electron spectroscopic study of the adsorption of molecular iodine on uranium metal and uranium dioxide

International Nuclear Information System (INIS)

Dillard, J.G.; Moers, H.; Klewe-Nebenius, H.; Kirch, G.; Pfennig, G.; Ache, H.J.

1984-01-01

The adsorption of molecular iodine on uranium metal and on uranium dioxide has been investigated at 25 0 C. Clean surfaces were prepared in an ultrahigh vacuum apparatus and were characterized by X-ray photoelectron (XPS) and X-ray and electron-induced Auger electron spectroscopies (AES). Adsorption of I 2 was studied for exposures up to 100 langmuirs (1 langmuir = 10 -6 torr s) on uranium metal and to 75 langmuirs on uranium dioxide. Above about 2-langmuir I 2 exposure on uranium, spectroscopic evidence is obtained to indicate the beginning of UI 3 formation. Saturation coverage for I 2 adsorption on uranium dioxide occurs at approximately 10-15 langmuirs. Analysis of the XPS and AES results as well as studies of spectra as a function of temperature lead to the conclusions that a dissociative chemisorption/reaction process occurs on uranium metal while nondissociative adsorption occurs on uranium dioxide. Variations in the iodine Auger kinetic energy and in the Auger parameter are interpreted in light of extra-atomic relaxation processes. 42 references, 10 figures, 1 table

On the interaction of uranium with the bioligands citric acid and glucose

International Nuclear Information System (INIS)

Steudtner, Robin

2011-01-01

For a better understanding of the actinide behaviour in human (in term of metabolism, retention, excretion) and in geological and biological systems, it is of prime importance to have a good knowledge of the relevant speciation. In model systems the chemical behaviour of uranium regarding complex formation and redox reaction were investigated. On this basis determinates thermodynamics constants and redox behaviour are used to prognoses a safety assessment for the respective system. The pentavalent uranium(V) is a metastable intermediate in natural redox system between uranium(IV) and uranium(VI). In this study the uranium(V) fluorescence was detected by laser spectroscopic methods (λ ex = 255 nm) for the first time. The peak maxima (λ ex = 255 nm) of luminescence spectrum of the photo reduced U(V) in aqueous perchlorate/2-propanol solution was detected at 440 nm and a fluorescence lifetime of 1.1 ± 0.02 μs was calculated. The stable aqueous uranyl(V)-tricarbonate complex was characterized by fluorescence spectroscopy (λ ex = 255 nm and 408 nm). The known quench effects of carbonate could be minimized by coupling the laser fluorescence system with the low temperature technique. The resulting U(V) fluorescence emission bands were detected between 375 nm and 445 nm. The peak maxima were identified at 401.5 nm (λ ex = 255 nm) and 413.0 nm (λ ex = 408 nm). The fluorescence lifetime of the uranyl(V)-carbonate species was determined at 153 K as 120 ± 0.1 μs (λ ex = 255 nm). In addition the fluorescence of uranium(V) was verifies by confocal laser scanning microscopy. The oxidation process from uranium(IV) to uranium(VI) was investigated on solid uraninite (UO 2 ) and uranium(IV) tetra chloride (UCl 4 ) and a 1 x 10 -2 M uranium(IV) sulphate (U IV SO 4 ) solution. By continuous oxygen transfer the uranium(IV) was oxidized slowly to uranium(VI). The temporal process was studied by the confocal laser scanning microscopy using an excitation wavelength of 408 nm. The

High-temperature helium-loop facility

International Nuclear Information System (INIS)

Tokarz, R.D.

1981-09-01

The high-temperature helium loop is a facility for materials testing in ultrapure helium gas at high temperatures. The closed loop system is capable of recirculating high-purity helium or helium with controlled impurities. The gas loop maximum operating conditions are as follows: 300 psi pressure, 500 lb/h flow rate, and 2100 0 F temperature. The two test sections can accept samples up to 3.5 in. diameter and 5 ft long. The gas loop is fully instrumented to continuously monitor all parameters of loop operation as well as helium impurities. The loop is fully automated to operate continuously and requires only a daily servicing by a qualified operator to replenish recorder charts and helium makeup gas. Because of its versatility and high degree of parameter control, the helium loop is applicable to many types of materials research. This report describes the test apparatus, operating parameters, peripheral systems, and instrumentation system. The experimental capabilities and test conand presents the results that have been obtained. The study has been conducted using a four-phase approach. The first phase develops the solution to the steady-state radon-diffusion equation in one-dimensieered barriers; disposal charge analysis; analysis of spent fuel policy implementation; spent f water. Field measurements and observations are reported for each site. Analytical data and field measurements are presented in tables and maps. Uranium concentrations in the sediments which were above detection limits ranged from 0.10 t 51.2 ppM. The mean of the logarithms of the uranium concentrations was 0.53. A group of high uranium concentrations occurs near the junctions of quadrangles AB, AC, BB, a 200 mK. In case 2), x-ray studies of isotopic phase separation in 3 He-- 4 He bcc solids were carried out by B. A. Fraass

Irradiation Stability of Uranium Alloys at High Exposures

International Nuclear Information System (INIS)

McDonell, W.R.

2001-01-01

Postirradiation examinations were begun of a series of unrestrained dilute uranium alloy specimens irradiated to exposures up to 13,000 MWD/T in NaK-containing stainless steel capsules. This test, part of a program of development of uranium metal fuels for desalination and power reactors sponsored by the Division of Reactor Development and Technology, has the objective of defining the temperature and exposure limits of swelling resistance of the alloyed uranium. This paper discusses those test results

Uranium mobilization from low-grade ore by cyanobacteria

International Nuclear Information System (INIS)

Lorenz, M.G.; Krumbein, W.E.

1985-01-01

Three cyanobacterial isolates (two LPP-B forms and one Anabaena or Nostoc species) from different environments could mobilize uranium from low-grade ores. After 80 days, up to 18% uranium had been extracted from coal and 51% from a carbonate rock by the filamentous cyanobacterium OL3, a LPP-B form. Low growth requirements with regard to light and temperature optima make this strain a possible candidate for leaching neutral and alkaline low-grade uranium ores. (orig.)

Uranium mobilization from low-grade ore by cyanobacteria

Energy Technology Data Exchange (ETDEWEB)

Lorenz, M.G.; Krumbein, W.E.

1985-04-01

Three cyanobacterial isolates (two LPP-B forms and one Anabaena or Nostoc species) from different environments could mobilize uranium from low-grade ores. After 80 days, up to 18% uranium had been extracted from coal and 51% from a carbonate rock by the filamentous cyanobacterium OL3, a LPP-B form. Low growth requirements with regard to light and temperature optima make this strain a possible candidate for leaching neutral and alkaline low-grade uranium ores.

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.

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.

Extraction behavior of uranium(VI) with polyurethane foam

International Nuclear Information System (INIS)

Tingchia Huang; Donghwang Chen; Muchang Shieh; Chingtsven Huang

1992-01-01

The extraction of uranium(VI) from aqueous solution with polyether-based polyurethane (PU) foam was studied. The effects of the kinds and concentrations of nitrate salts, uranium(VI) concentration, temperature, nitric acid concentration, pH, the content of poly(ethylene oxide) in the polyurethane foam, and the ratio of PU foam weight and solution volume on the extraction of uranium(VI) were investigated. The interferences of fluoride and carbonate ions on the extraction of uranium(VI) were also examined, and methods to overcome both interferences were suggested. It was found that no uranium was extracted in the absence of a nitrate salting-out agent, and the extraction behaviors of uranium(IV) with polyurethane foam could be explained in terms of an etherlike solvent extraction mechanism. In addition, the percentage extraction of a multiple stage was also estimated theoretically

Extractive spectrophotometric determination of uranium with malachite green

Energy Technology Data Exchange (ETDEWEB)

Dubey, S C; Nadkarni, M N [Bhabha Atomic Research Centre, Bombay (India). Fuel Reprocessing Div.

1977-04-01

A sensitive spectrophotometric method based on the extraction of a uranium-benzoate-Malachite Green complex by chlorobenzene is described. The absorption maximum is at 635 nm and the molar absorptivity is 8.3 x 10/sup 4/1. mole /sup -1/ cm/sup -1/. A preliminary separation of uranium by extraction with methyl isobutyl ketone from acid-deficient aluminium nitrate solution is used to avoid interferences. An aliquot of the extract in then diluted with chlorobenzene and shaken with benzoate buffer containing Malachite Green (MG). The method has been applied for the determination of uranium in a synthetic leach solution. The complex extracted is probably (U0/sub 2/(C/sub 6/H/sub 5/C00/sub 3//sup -/)(MG/sup +/).

Comparative Study of Regional Estimation Methods for Daily Maximum Temperature (A Case Study of the Isfahan Province

Directory of Open Access Journals (Sweden)

Ghamar Fadavi

2016-02-01

Full Text Available Introduction: As the statistical time series are in short period and the meteorological station are not distributed well in mountainous area determining of climatic criteria are complex. Therefore, in recent years interpolation methods for establishment of continuous climatic data have been considered. Continuous daily maximum temperature data are a key factor for climate-crop modeling which is fundamental for water resources management, drought, and optimal use from climatic potentials of different regions. The main objective of this study is to evaluate different interpolation methods for estimation of regional maximum temperature in the Isfahan province. Materials and Methods: Isfahan province has about 937,105 square kilometers, between 30 degree and 43 minutes to 34 degree and 27 minutes North latitude equator line and 49 degree and 36 minutes to 55 degree and 31 minutes east longitude Greenwich. It is located in the center of Iran and it's western part extend to eastern footage of the Zagros mountain range. It should be mentioned that elevation range of meteorological stations are between 845 to 2490 in the study area. This study was done using daily maximum temperature data of 1992 and 2007 years of synoptic and climatology stations of I.R. of Iran meteorological organization (IRIMO. In order to interpolate temperature data, two years including 1992 and 2007 with different number of meteorological stations have been selected the temperature data of thirty meteorological stations (17 synoptic and 13 climatologically stations for 1992 year and fifty four meteorological stations (31 synoptic and 23 climatologically stations for 2007 year were used from Isfahan province and neighboring provinces. In order to regionalize the point data of daily maximum temperature, the interpolation methods, including inverse distance weighted (IDW, Kriging, Co-Kriging, Kriging-Regression, multiple regression and Spline were used. Therefore, for this allocated

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

International Nuclear Information System (INIS)

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

2002-01-01

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

Depleted uranium hexafluoride: Waste or resource?

Energy Technology Data Exchange (ETDEWEB)

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

1995-07-01

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

Liquid uranium contaimment in refractories metals

International Nuclear Information System (INIS)

Duarte, J.L.; Padilha, A.F.

1982-01-01

Tests were performed on metalic materials for liquid uranium containment up to 2100 0 C. The materials Nb, Mo, Ta and W in the form of crucibles were tested at 2100 0 C for one hour in the presence of flowing argon. After testing, the crucibles were etched using HCl and analysed by optical metallography and electron proble microanalysis. The results are discussed in terms of Berthoud equation and indicated that the solubility limit of the crucible material in uranium at the temperature controlls the crucible dissolution by liquid uranium. The various phases formed, the mechanism of dissolution and the possible material for future use are presented and discussed. (Author) [pt

Method for the production of uranium chloride salt

Science.gov (United States)

Westphal, Brian R.; Mariani, Robert D.

2013-07-02

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

Separation of uranium isotopes

International Nuclear Information System (INIS)

Porter, J.T.

1980-01-01

Methods and apparatus are disclosed for separation of uranium isotopes by selective isotopic excitation of photochemically reactive uranyl salt source material at cryogenic temperatures, followed by chemical separation of selectively photochemically reduced U+4 thereby produced from remaining uranyl source material

Quantification of the effect of in-situ generated uranium metal on the experimentally determined O/U ratio of a sintered uranium dioxide fuel pellet

International Nuclear Information System (INIS)

Narasimha Murty, B.; Bharati Misra, U.; Yadav, R.B.; Srivastava, R.K.

2005-01-01

This paper describes quantitatively the effect of in-situ generated uranium metal (that could be formed due to the conducive manufacturing conditions) in a sintered uranium dioxide fuel pellet on the experimentally determined O/U ratio using analytical methods involving dissolution of the pellet material. To quantify the effect of in-situ generated uranium metal in the fuel pellet, a mathematical expression is derived for the actual O/U ratio in terms of the O/U ratio as determined by an experiment involving dissolution of the material and the quantity of uranium metal present in the uranium dioxide pellet. The utility of this derived mathematical expression is demonstrated by tabulating the calculated actual O/U ratios for varying amounts of uranium metal (from 5 to 95% in 5% intervals) and different O/U ratio values (from 2.001 to 2.015 in 0.001 intervals). This paper brings out the necessity of care to be exercised while interpreting the experimentally determined O/U ratio and emphasizes the fact that it is always safer to produce the nuclear fuel with oxygen to uranium ratios well below the specified maximum limit of 2.015. (author)

Probing Ionic Liquid Aqueous Solutions Using Temperature of Maximum Density Isotope Effects

Directory of Open Access Journals (Sweden)

Mohammad Tariq

2013-03-01

Full Text Available This work is a new development of an extensive research program that is investigating for the first time shifts in the temperature of maximum density (TMD of aqueous solutions caused by ionic liquid solutes. In the present case we have compared the shifts caused by three ionic liquid solutes with a common cation—1-ethyl-3-methylimidazolium coupled with acetate, ethylsulfate and tetracyanoborate anions—in normal and deuterated water solutions. The observed differences are discussed in terms of the nature of the corresponding anion-water interactions.

Extraction and determination of hydrogen in uranium and zirconium; Extraction et dosage de l'hydrogene dans l'uranium et le zirconium

Energy Technology Data Exchange (ETDEWEB)

Champeix, L; Coblence, G; Darras, R [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

1959-07-01

The method of desorption under vacuum at high temperatures in the solid phase, which gives good results in the case of steels, has been applied to uranium and zirconium. In these two metals hydrogen is found mainly in the form of hydride. It is chiefly a question of determining the most suitable temperature and the heating time necessary to obtain an almost total extraction of hydrogen. Two considerations must be taken into account in the choice of temperature. It should be such that on the one hand the hydride decomposes rapidly and completely at the reduced pressure applied, and on the other hand the diffusion of hydrogen through the metal takes place fairly quickly. The apparatus and the method used are described; systematic tests have led to the adoption of temperatures of 650 deg. C for uranium and 1050 deg. C for zirconium. (author) [French] La methode de desorption sous vide a chaud en phase solide, methode qui donne de bons resultats dans le cas des aciers, a ete appliquee a l'uranium et au zirconium. Dans ces deux metaux, l'hydrogene se trouve surtout a l'etat d'hydrure. Il s'agit essentiellement de determiner la temperature optimum et la duree du chauffage necessaire pour obtenir une extraction d'hydrogene pratiquement complete. Deux considerations interviennent dans le choix de la temperature. Elle doit etre telle que, d'une part la decomposition de l'hydrure se fasse rapidement et completement sous la pression reduite realisee et d'autre part que la diffusion de l'hydrogene a travers le metal soit assez rapide. L'appareil et le mode operatoire utilises sont decrits des essais systematiques ont conduit a adopter une temperature de 650 deg. C pour l'uranium et de 1050 deg. C pour le zirconium. (auteur)

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.

Impact of soil moisture on extreme maximum temperatures in Europe

Directory of Open Access Journals (Sweden)

Kirien Whan

2015-09-01

Full Text Available Land-atmosphere interactions play an important role for hot temperature extremes in Europe. Dry soils may amplify such extremes through feedbacks with evapotranspiration. While previous observational studies generally focused on the relationship between precipitation deficits and the number of hot days, we investigate here the influence of soil moisture (SM on summer monthly maximum temperatures (TXx using water balance model-based SM estimates (driven with observations and temperature observations. Generalized extreme value distributions are fitted to TXx using SM as a covariate. We identify a negative relationship between SM and TXx, whereby a 100 mm decrease in model-based SM is associated with a 1.6 °C increase in TXx in Southern-Central and Southeastern Europe. Dry SM conditions result in a 2–4 °C increase in the 20-year return value of TXx compared to wet conditions in these two regions. In contrast with SM impacts on the number of hot days (NHD, where low and high surface-moisture conditions lead to different variability, we find a mostly linear dependency of the 20-year return value on surface-moisture conditions. We attribute this difference to the non-linear relationship between TXx and NHD that stems from the threshold-based calculation of NHD. Furthermore the employed SM data and the Standardized Precipitation Index (SPI are only weakly correlated in the investigated regions, highlighting the importance of evapotranspiration and runoff for resulting SM. Finally, in a case study for the hot 2003 summer we illustrate that if 2003 spring conditions in Southern-Central Europe had been as dry as in the more recent 2011 event, temperature extremes in summer would have been higher by about 1 °C, further enhancing the already extreme conditions which prevailed in that year.

PRODUCTION OF URANIUM TUBING

Science.gov (United States)

Creutz, E.C.

1958-04-15

The manufacture of thin-walled uranium tubing by the hot-piercing techique is described. Uranium billets are preheated to a temperature above 780 d C. The heated billet is fed to a station where it is engaged on its external surface by three convex-surfaced rotating rollers which are set at an angle to the axis of the billet to produce a surface friction force in one direction to force the billet over a piercing mandrel. While being formed around the mandrel and before losing the desired shape, the tube thus formed is cooled by a water spray.

Thermodynamics of the uranium (α, β and γ phases)-hydrogen system

International Nuclear Information System (INIS)

Northrup, C.J.M. Jr.

1975-01-01

Pressure-composition isotherms have been obtained for the uranium-hydrogen system over the pressure range from 0.1 to 680 atmospheres at temperatures ranging from 450 to 846 0 C. The hydride (delta) was formed from high purity uranium and pressure--temperature plots were obtained for the (U/sub alpha/, delta), (U/sub beta/, delta), (U/sub gamma/, delta) two phase regions. Results of the investigation indicate that in contrast to the work of Chevallier, Spitz, and Blum [Chevallier et al., Acad. Sci., 264: 96(1967)], the uranium-hydrogen system retains broad, flat, two phase plateaus on the pressure-composition isotherms to temperatures as high as 846 0 C. The effect of oxygen impurities is noted and it was found that the enthalpy of formation of the hydride from pure uranium was -28.9 kcal mol -1 . The three dimensional phase diagram for the system is discussed and the gas-liquid, gas-solid interface is given delineating the known phase boundaries. (U.S.)

Uranium concentrations in the water consumed by the resident population in the vicinity of the Lagoa Real uranium province, Bahia, Brazil

Energy Technology Data Exchange (ETDEWEB)

Silva, Luciana S. [State University of Bahia (UNEB), Campus Caetite, BA (Brazil); Pecequilo, Brigitte R.S.; Sarkis, Jorge; Nisti, Marcelo B., E-mail: brigitte@ipen.br, E-mail: jesarkis@ipen.br, E-mail: mbnisti@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

2011-07-01

The Lagoa Real Uranium Province, situated in South Central Bahia in the region of Caetite and Lagoa Real, is considered the most important monomineralic province of Brazil. The urban population who lives in the proximities of this uranium province in the cities of Caetite, Lagoa Real and Livramento uses public supply water, while the inhabitants of the rural area due to long terms of dry weather use water from wells, cisterns, small dams, reservoirs and dikes which are supplied with the rains. In this work it was determined the concentration of uranium in the water consumed by the rural and urban population living in the proximities of the Lagoa Real Uranium Province. The study comprehends 32 sampling spots spread throughout the region of interest. Samples were collected in January and July 2010, covering superficial, underground and public supply water from the region. The uranium concentrations were determined by an inductively coupled plasma mass spectrometer (ICP-MS). Preliminary results showed that the uranium concentrations in the water from the Lagoa Real Uranium Province varied from 0.064 {+-} 0.005 {mu}g.L{sup -1} to 90 {+-} 1,5 {+-}g.L{sup -1}. It was observed that only two of them obtained values higher than the World Health Organization's recommended limit (2011) of 30 {mu}g.L{sup -1} for maximum uranium concentration in the water for human consumption. For a conclusive evaluation, the uranium concentrations results will be analyzed together with total alpha and beta concentrations determined elsewhere for the same samples. (author)

Uranium concentrations in the water consumed by the resident population in the vicinity of the Lagoa Real uranium province, Bahia, Brazil

International Nuclear Information System (INIS)

Silva, Luciana S.; Pecequilo, Brigitte R.S.; Sarkis, Jorge; Nisti, Marcelo B.

2011-01-01

The Lagoa Real Uranium Province, situated in South Central Bahia in the region of Caetite and Lagoa Real, is considered the most important monomineralic province of Brazil. The urban population who lives in the proximities of this uranium province in the cities of Caetite, Lagoa Real and Livramento uses public supply water, while the inhabitants of the rural area due to long terms of dry weather use water from wells, cisterns, small dams, reservoirs and dikes which are supplied with the rains. In this work it was determined the concentration of uranium in the water consumed by the rural and urban population living in the proximities of the Lagoa Real Uranium Province. The study comprehends 32 sampling spots spread throughout the region of interest. Samples were collected in January and July 2010, covering superficial, underground and public supply water from the region. The uranium concentrations were determined by an inductively coupled plasma mass spectrometer (ICP-MS). Preliminary results showed that the uranium concentrations in the water from the Lagoa Real Uranium Province varied from 0.064 ± 0.005 μg.L -1 to 90 ± 1,5 ±g.L -1 . It was observed that only two of them obtained values higher than the World Health Organization's recommended limit (2011) of 30 μg.L -1 for maximum uranium concentration in the water for human consumption. For a conclusive evaluation, the uranium concentrations results will be analyzed together with total alpha and beta concentrations determined elsewhere for the same samples. (author)

Can we predict uranium bioavailability based on soil parameters? Part 1: Effect of soil parameters on soil solution uranium concentration

International Nuclear Information System (INIS)

Vandenhove, H.; Hees, M. van; Wouters, K.; Wannijn, J.

2007-01-01

Present study aims to quantify the influence of soil parameters on soil solution uranium concentration for 238 U spiked soils. Eighteen soils collected under pasture were selected such that they covered a wide range for those parameters hypothesised as being potentially important in determining U sorption. Maximum soil solution uranium concentrations were observed at alkaline pH, high inorganic carbon content and low cation exchange capacity, organic matter content, clay content, amorphous Fe and phosphate levels. Except for the significant correlation between the solid-liquid distribution coefficients (K d , L kg -1 ) and the organic matter content (R 2 = 0.70) and amorphous Fe content (R 2 = 0.63), there was no single soil parameter significantly explaining the soil solution uranium concentration (which varied 100-fold). Above pH = 6, log(K d ) was linearly related with pH [log(K d ) = - 1.18 pH + 10.8, R 2 = 0.65]. Multiple linear regression analysis did result in improved predictions of the soil solution uranium concentration but the model was complex. - Uranium solubility in soil can be predicted from organic matter or amorphous iron content and pH or with complex multilinear models considering several soil parameters

The uranium dioxide-uranium system at high temperature; Le systeme uranium-dioxyde d'uranium a haute temperature

Energy Technology Data Exchange (ETDEWEB)

Guinet, Ph.; Vaugoyeau, H.; Blum, P. [Commissariat a l' Energie Atomique, Grenoble (France). Centre d' Etudes Nucleaires

1966-07-01

The liquidus curve has been determined by a saturation method in which the thermal gradient was cancelled upon cooling, and the solidus curve by analyzing the deposits in equilibrium with the liquid at each temperature. The diagram, of a displaced eutectic type, presents a liquid immiscibility domain between 47 and 59 mol per cent of dioxide and a substoichiometry range UO{sub 2x}, the minimum O/U ratio being 1,6 at 3470 {+-} 30 C. The monotectic composition was found by chemical analysis to be 59 mol per cent of dioxide and the reaction temperature 2470 {+-} 30 C. (author) [French] La courbe liquidus a ete determinee par une methode de saturation en annulant le gradient thermique au cours du refroidissement, la courbe solidus par analyse des depots en equilibre avec le liquide a chaque temperature. Le diagramme du type a eutectique deporte comporte un domaine d'immiscibilite liquide entre 47 et 59 moles pour cent de dioxyde, ainsi qu'un domaine d'existence du compose sous stoechiometrique UO{sub 2x}, le rapport O/U minimum etant egal a 1,6 a 2470 {+-} 30 C. La composition du monotectique, obtenue par analyse chimique, est de 59 moles pour cent de dioxyde et la temperature de la reaction a ete trouvee egale a 2470 {+-} 30 C. (auteur)

Uranium concentrations in groundwater, northeastern Washington

Science.gov (United States)

Kahle, Sue C.; Welch, Wendy B.; Tecca, Alison E.; Eliason, Devin M.

2018-04-18

A study of uranium in groundwater in northeastern Washington was conducted to make a preliminary assessment of naturally occurring uranium in groundwater relying on existing information and limited reconnaissance sampling. Naturally occurring uranium is associated with granitic and metasedimentary rocks, as well as younger sedimentary deposits, that occur in this region. The occurrence and distribution of uranium in groundwater is poorly understood. U.S. Environmental Protection Agency (EPA) regulates uranium in Group A community water systems at a maximum contaminant level (MCL) of 30 μg/L in order to reduce uranium exposure, protect from toxic kidney effects of uranium, and reduce the risk of cancer. However, most existing private wells in the study area, generally for single family use, have not been sampled for uranium. This document presents available uranium concentration data from throughout a multi-county region, identifies data gaps, and suggests further study aimed at understanding the occurrence of uranium in groundwater.The study encompasses about 13,000 square miles (mi2) in the northeastern part of Washington with a 2010 population of about 563,000. Other than the City of Spokane, most of the study area is rural with small towns interspersed throughout the region. The study area also includes three Indian Reservations with small towns and scattered population. The area has a history of uranium exploration and mining, with two inactive uranium mines on the Spokane Indian Reservation and one smaller inactive mine on the outskirts of Spokane. Historical (1977–2016) uranium in groundwater concentration data were used to describe and illustrate the general occurrence and distribution of uranium in groundwater, as well as to identify data deficiencies. Uranium concentrations were detected at greater than 1 microgram per liter (μg/L) in 60 percent of the 2,382 historical samples (from wells and springs). Uranium concentrations ranged from less than 1 to

THE MAXIMUM EFFECT OF DEEP LAKES ON TEMPERATURE PROFILES – DETERMINATION OF THE GEOTHERMAL GRADIENT

Directory of Open Access Journals (Sweden)

Eppelbaum L. V.

2009-07-01

Full Text Available Understanding the climate change processes on the basis of geothermal observations in boreholes is an important and at the same time high-intricate problem. Many non-climatic effects could cause changes in ground surface temperatures. In this study we investigate the effects of deep lakes on the borehole temperature profilesobserved within or in the vicinity of the lakes. We propose a method based on utilization of Laplace equation with nonuniform boundary conditions. The proposed method makes possible to estimate the maximum effect of deep lakes (here the term "deep lake" means that long term mean annual temperature of bottom sediments can beconsidered as a constant value on the borehole temperature profiles. This method also allows one to estimate an accuracy of the determination of the geothermal gradient.

Uranium biosorption by Trichoderma harzianum entrapped in polyester foam beads

International Nuclear Information System (INIS)

Khalid, A.M.; Shemsi, A.M.; Akhtar, K.; Anwar, M.A.

1993-01-01

Mechanism of uranium biosorption by resting cells of Trichoderma harzianum was studied at pH 4.5. Time-dependent uptake of uranium by Trichoderma harzianum was also determined. Various cations (Na, K, Ca and Fe, etc.) were found to affect the adsorption capability of these cells. Different theoretical thermodynamic models governing the adsorption behavior of uranium were also tested and it was found to follow the Langmuir and Freundlich adsorption isotherms. The constants of Freundlich adsorption isotherm A and 1/n were found to be 1.5 x 10 -6 mole/g and 0.31 respectively. Dubinin Radushkevich equation was tested and the maximum adsorption capacity (X m ) of Trichoderma harzianum and sorption energy (E s ) for the ion exchange process computed. Data of uranium sorption were also examined using Weber Morris's equation. The upscaling of uranium biosorption by Trichoderma harzianum entrapped in commercial foam (polyesters) was carried out in glass columns. It was found to recover more than 85% of the total uranium present in bacterial leachate

Criticality safety considerations for MSRE fuel drain tank uranium aggregation

International Nuclear Information System (INIS)

Hollenbach, D.F.; Hopper, C.M.

1997-01-01

This paper presents the results of a preliminary criticality safety study of some potential effects of uranium reduction and aggregation in the Molten Salt Reactor Experiment (MSRE) fuel drain tanks (FDTs) during salt removal operations. Since the salt was transferred to the FDTs in 1969, radiological and chemical reactions have been converting the uranium and fluorine in the salt to UF 6 and free fluorine. Significant amounts of uranium (at least 3 kg) and fluorine have migrated out of the FDTs and into the off-gas system (OGS) and the auxiliary charcoal bed (ACB). The loss of uranium and fluorine from the salt changes the chemical properties of the salt sufficiently to possibly allow the reduction of the UF 4 in the salt to uranium metal as the salt is remelted prior to removal. It has been postulated that up to 9 kg of the maximum 19.4 kg of uranium in one FDT could be reduced to metal and concentrated. This study shows that criticality becomes a concern when more than 5 kg of uranium concentrates to over 8 wt% of the salt in a favorable geometry

Ionic Liquids as templating agents in formation of uranium-containing nanomaterials

Science.gov (United States)

Visser, Ann E; Bridges, Nicholas J

2014-06-10

A method for forming nanoparticles containing uranium oxide is described. The method includes combining a uranium-containing feedstock with an ionic liquid to form a mixture and holding the mixture at an elevated temperature for a period of time to form the product nanoparticles. The method can be carried out at low temperatures, for instance less than about 300.degree. C.

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

Study of reactions for the production of uranium titrafluoride and uranium hexafluoride

International Nuclear Information System (INIS)

Guzella, M.F.R.

1985-01-01

The main production processes of uranium hexafluoride in pilot plants and industrial facilities are described. The known reactions confirmed in laboratory experiments that lead to Uf 6 or other intermediate fluorides are discussed. For the purpose of determining a thermodinamically feasible reaction involving the sulfur hexafluoride as fluorinating agent, a mock-up facility was designed and constructed as a part of the R and D work planned at the CDTN (Nuclebras Center for Nuclear Technology Development). IN the uranium tatrafluoride synthesis employing U 3 O 8 and SF 6 several experimental parameters are studied. The reaction time, gasflow, temperature and stoechiometic relations among reagents are described in detail. (Author) [pt

Hyperspectral Alteration Information from Drill Cores and Deep Uranium Exploration in the Baiyanghe Uranium Deposit in the Xuemisitan Area, Xinjiang, China

Directory of Open Access Journals (Sweden)

Qing-Jun Xu

2017-05-01

Full Text Available The Baiyanghe uranium deposit is a currently important medium-sized deposit in the Xuemisitan area, Xinjiang. The hydrothermal alteration in this deposit is closely related to the uranium mineralization of the deposit. In this study, hyperspectral data are collected from drill cores in the Baiyanghe uranium deposit using a FieldSpec4 visible-shortwave infrared spectrometer to study the hydrothermal alteration. The results reveal that the altered mineral assemblages have obvious zonation characteristics: (1 the upper section comprises long-wavelength illite and minor hematite and montmorillonite; (2 the middle section contains three types of illite (long-, medium- and short-wavelength illite and hematite; and (3 the lower section includes short-wavelength illite, chlorite and carbonate. Additionally, the variety in the characteristic absorption-peak wavelength of illite at 2200 nm gradually shifts to shorter wavelength and ranges between 2195 nm and 2220 nm with increasing depth, while the SWIR-IC (short-wavelength infrared illite crystallinity, a dimensionless quantity of the drill holes gradually increases from 0.2 to 2.1. These patterns reflect the hydrothermal fluid activity in the deposit, which features relatively high-temperature, high-pressure hydrothermal fluid in the deeper section and low-temperature, low-pressure hydrothermal fluid in the shallower section. Additionally, the uranium mineralization is located near the fracture zone, which represents the center of hydrothermal fluid activity or mineralization. This area has abundant alteration minerals, and the minerals illite (short- and medium-wavelength, hematite and fluorite can be used as uranium-prospecting indicators for uranium exploration in the deeper sections of the Baiyanghe uranium deposit.

Uranium and radon in wells drilled into bedrock in Southern Finland

International Nuclear Information System (INIS)

Juntunen, R.

1991-01-01

More than 1000 samples of groundwater were taken from drilled wells in Southern Finland in 1982-1986 and submitted to chemical analyses that included the determination of uranium and radon abundances in the water. The waters were divided into eight groups by dominant rock type to establish the influence of the geological environment of the water. The median radon abundance for the total data on the drilled wells in southern Finland was 210 Bq/l, and that of uranium 5 ppb. The maximum uranium abundance was 20 000 ppb and that of radon about 50 000 Bq/l

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

Acidic aqueous uranium electrodeposition for target fabrication

International Nuclear Information System (INIS)

Saliba-Silva, A.M.; Oliveira, E.T.; Garcia, R.H.L.; Durazzo, M.

2013-01-01

Direct irradiation of targets inside nuclear research or multiple purpose reactors is a common route to produce 99 Mo- 99m Tc radioisotopes. The electroplating of low enriched uranium over nickel substrate might be a potential alternative to produce targets of 235 U. The electrochemistry of uranium at low temperature might be beneficial for an alternative route to produce 99 Mo irradiation LEU targets. Electrodeposition of uranium can be made using ionic and aqueous solutions producing uranium oxide deposits. The performance of uranium electrodeposition is relatively low because a big competition with H 2 evolution happens inside the window of electrochemical reduction potential. This work explores possibilities of electroplating uranium as UO 2 2+ (Uranium-VI) in order to achieve electroplating uranium in a sufficient amount to be commercially irradiated in the future Brazilian RMB reactor. Electroplated nickel substrate was followed by cathodic current electrodeposition from aqueous UO 2 (NO 3 ) 2 solution. EIS tests and modeling showed that a film formed differently in the three tested cathodic potentials. At the lower level, (-1.8V) there was an indication of a double film formation, one overlaying the other with ionic mass diffusion impaired at the interface with nickel substrate as showed by the relatively lower admittance of Warburg component. (author)

Microbial uptake of uranium, cesium, and radium

Energy Technology Data Exchange (ETDEWEB)

Strandberg, G.W.; Shumate, S.E. II; Parrott, J.R. Jr.; McWhirter, D.A.

1980-01-01

The ability of diverse microbial species to concentrate uranium, cesium, and radium was examined. Saccharomyces cerevisiae, Pseudomonas aeruginosa, and a mixed culture of denitrifying bacteria accumulated uranium to 10 to 15% of the dry cell weight. Only a fraction of the cells in a given population had visible uranium deposits in electron micrographs. While metabolism was not required for uranium uptake, mechanistic differences in the metal uptake process were indicated. Uranium accumulated slowly (hours) on the surface of S. cerevisiae and was subject to environmental factors (i.e., temperature, pH, interfering cations and anions). In contrast, P. aeruginosa and the mixed culture of denitrifying bacteria accumulated uranium rapidly (minutes) as dense, apparently random, intracellular deposits. This very rapid accumulation has prevented us from determining whether the uptake rate during the transient between the initial and equilibrium distribution of uranium is affected by environmental conditions. However, the final equilibrium distributions are not affected by those conditions which affect uptake by S. cerevisiae. Cesium and radium were concentrated to a considerably lesser extent than uranium by the several microbial species tested. The potential utility of microorganisms for the removal and concentration of these metals from nuclear processing wastes and several bioreactor designs for contacting microorganisms with contaminated waste streams will be discussed.

Aluminum-Oxide Temperatures on the Mark VB, VE, VR, 15, and Mark 25 Assemblies

International Nuclear Information System (INIS)

Aleman, S.E.

2001-01-01

The task was to compute the maximum aluminum-oxide and oxide-coolant temperatures of assemblies cladded in 99+ percent aluminum. The assemblies considered were the Mark VB, VE, V5, 15 and 25. These assemblies consist of nested slug columns with individual uranium slugs cladded in aluminum cans. The CREDIT code was modified to calculate the oxide film thickness and the aluminum-oxide temperature at each axial increment. This information in this report will be used to evaluate the potential for cladding corrosion of the Mark 25 assembly

A study of uranium adsorption to single-crystal tungsten

Energy Technology Data Exchange (ETDEWEB)

Samin, Adib; Hastings, Aaron; Zhang, Jinsuo, E-mail: jzhang@osu.edu

2015-12-15

In this study we explore the adsorption of uranium to the (110) plane of tungsten. Potential functions were constructed to describe the interaction of adsorbed uranium atoms with the tungsten surface and the lateral interaction between adsorbed uranium atoms. Next, the behavior of the uranium adlayer under different conditions was studied through a Monte Carlo simulation of the grand canonical Hamiltonian in an off-lattice model. Our results are consistent with available studies in the literature. The simulation results indicate that the temperature and dipole–dipole interactions play an important role in governing the adsorption process.

A study of uranium adsorption to single-crystal tungsten

International Nuclear Information System (INIS)

Samin, Adib; Hastings, Aaron; Zhang, Jinsuo

2015-01-01

In this study we explore the adsorption of uranium to the (110) plane of tungsten. Potential functions were constructed to describe the interaction of adsorbed uranium atoms with the tungsten surface and the lateral interaction between adsorbed uranium atoms. Next, the behavior of the uranium adlayer under different conditions was studied through a Monte Carlo simulation of the grand canonical Hamiltonian in an off-lattice model. Our results are consistent with available studies in the literature. The simulation results indicate that the temperature and dipole–dipole interactions play an important role in governing the adsorption process.

Adsorption behavior and mechanism of uranium on wood fiber

International Nuclear Information System (INIS)

Wang Zhe; Yi Facheng; Feng Yuan

2015-01-01

The adsorption performance of uranium on wood fiber was studied with static experiment. The influence factors on the U(Ⅵ) removal rate such as wood fiber particle size, adsorption time, dosage, temperature, pH and initial concentration were researched, and the adsorption process was analyzed in terms of thermodynamics and kinetics. The results show that the adsorption equilibrium time is 4 hours. When the pH reaches 3 for uranium-containing wastewater, uranium can be removed with the decrease of the size of adsorbent and with the increase of adsorbent dosage and temperature. The equilibrium adsorption data fit to Langmuir isotherms. The kinetic analysis shows that the adsorption rate is mainly controlled by chemical adsorption. The adsorption process can be described by an equation of pseudo 2nd-order model. The thermodynamic data indicate that the synergistic uranium bio-sorption by wood fiber is a spontaneous and endothermal adsorption process. The adsorption mechanism was analyzed with SEM, FT-IR and EDS. The results show that the surface form of wood fiber is changed and uranium mainly chelates with active groups on the fiber-s surface and forms the complexes. These indicate that the adsorption of uranium should be of surface coordination. The analyses of EDS before and after adsorption of uranium prove that the behavior of adsorption is ion exchange. The above results indicate that the adsorption mechanism is mainly surface coordination and ion exchange adsorption, followed by physical absorption. (authors)

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

International Nuclear Information System (INIS)

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

1982-01-01

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

Tectonic stress history and the relationship with uranium mineralization in Shenchong mining area

International Nuclear Information System (INIS)

Zhu Mingqiang; Lin Yinshan; Kang Zili

1996-01-01

The rejection method of maximum statistical for principal stress axis is applied to complex granite body, this paper divide mining area tectonic process into six epochs. The relationship between the tectonic process and uranium mineralization is also discussed, and the later 3 times fracture process of Diwa epoch control the removing and gathering of Uranium in this area

Evaluation of the LASL automated spectrophotometer for uranium determination at submilligram levels

International Nuclear Information System (INIS)

Hollen, R.M.; Jackson, D.D.; Rein, J.E.

1977-07-01

The LASL automated spectrophotometer, designed for determination of 1 to 14 mg of uranium and 0.5 to 14 mg of plutonium, has been evaluated for determination of lower levels of uranium to 0.12 mg. The essentially linear response of absorbance is maintained and the standard deviation for a single measurement is constant at about 0.013 mg of uranium, corresponding to a maximum uncertainty of about 10 percent at the 0.12-mg limit. The instrument was applied to the analysis of a series of low-level-concentration, 0.07- to 0.8-mg/ml uranium samples. The results were not statistically different from those obtained by a manual spectrophotometric method

Equilibrium, kinetic and thermodynamic studies of uranium biosorption by calcium alginate beads

International Nuclear Information System (INIS)

Bai, Jing; Fan, Fangli; Wu, Xiaolei; Tian, Wei; Zhao, Liang; Yin, Xiaojie; Fan, Fuyou; Li, Zhan; Tian, Longlong; Wang, Yang; Qin, Zhi; Guo, Junsheng

2013-01-01

Calcium alginate beads are potential biosorbent for radionuclides removal as they contain carboxyl groups. However, until now limited information is available concerning the uptake behavior of uranium by this polymer gel, especially when sorption equilibrium, kinetics and thermodynamics are concerned. In present work, batch experiments were carried out to study the equilibrium, kinetics and thermodynamics of uranium sorption by calcium alginate beads. The effects of initial solution pH, sorbent amount, initial uranium concentration and temperature on uranium sorption were also investigated. The determined optimal conditions were: initial solution pH of 3.0, added sorbent amount of 40 mg, and uranium sorption capacity increased with increasing initial uranium concentration and temperature. Equilibrium data obtained under different temperatures were fitted better with Langmuir model than Freundlich model, uranium sorption was dominated by a monolayer way. The kinetic data can be well depicted by the pseudo-second-order kinetic model. The activation energy derived from Arrhenius equation was 30.0 kJ/mol and the sorption process had a chemical nature. Thermodynamic constants such as ΔH 0 , ΔS 0 and ΔG 0 were also evaluated, results of thermodynamic study showed that the sorption process was endothermic and spontaneous. -- Highlights: • Equilibrium, kinetics and thermodynamics of uranium sorption by CaAlg were studied. • Equilibrium studies show that Langmuir isotherm better fit with experimental data. • Pseudo-second-order kinetics model is found to be well depicting the kinetic data. • Thermodynamic study shows that the sorption process is endothermic and spontaneous

Waste arisings from a high-temperature reactor with a uranium-thorium fuel cycle

International Nuclear Information System (INIS)

1979-09-01

This paper presents an equilibrium-recycle condition flow sheet for a high-temperature gas-cooled reactor (HTR) fuel cycle which uses thorium and high-enriched uranium (93% U-235) as makeup fuel. INFCE Working Group 7 defined percentage losses to various waste streams are used to adjust the heavy-element mass flows per gigawatt-year of electricity generated. Thorium and bred U-233 are recycled following Thorex reprocessing. Fissile U-235 is recycled one time following Purex reprocessing and then is discarded to waste. Plutonium and other transuranics are discarded to waste. Included are estimates of volume, radioactivity, and heavy-element content of wastes arising from HTR fuel element fabrication; HTR operation, maintenance, and decommissioning; and reprocessing spent fuel where the waste is unique to the HTR fuel cycle

Uranium exploration planning and strategy

International Nuclear Information System (INIS)

Smith, A.Y.; Tauchid, M.

1991-01-01

A country may decide to begin uranium exploration for any of the following three reasons: 1. To meet the needs of a domestic nuclear power programme; 2. To supply uranium as a commodity to the world market in order to earn foreign exchange; 3. To acquire national information on the country's mineral resource planning. In any of these cases, a country must make some basic decisions regarding the means and modes whereby the uranium exploration will be carried out - by national organizations exclusively; by state organizations in joint venture with outside interests by foreign interests under the control of national regulations. Most uranium exploration is carried out following an exploration strategy in which the programme is divided into a series of steps or stages. Each of the phases is designed to eliminate areas of low potential to contain uranium deposits, while focusing attention on areas of higher potential that will be explored in greater detail at higher cost in the subsequent phase. The methods used in each phase are selected to provide the maximum information at the minimum cost so that at the end of each phase a decision can be made whether to continue to the next phase of stop. Because uranium exploration is a high cost high risk activity, governments must make decisions at the outset whether they wish to carry our the work alone and whether they can support the costs involved, or whether they wish to attract foreign investors to help absorb the costs and therefore the risks. In either case, major policy decisions are required to be made to establish the legal and fiscal environment in which the programm will be carried out. (author). 4 refs, 4 figs

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

Solvent extraction of uranium (VI) by Amberlite Lsub(A-1)

International Nuclear Information System (INIS)

Kim, S.S.

1977-01-01

The effects of uranium, amine and sulfuric acid concentrate, and temperature on the extraction of uranium(VI) from acidic sulphate solutions by Amberlite Lsub(A-1) in benzene was studied. The extraction of sulfuric acid by Amberlite Lsub(A-1) in benzene was also examined. It was found that 92 to 98 percent extraction was obtained for a uranyl sulphate solution of 5g/1 concentrate containing of 0.2M to 0.3M sulfuric acid, a Amberlite Lsub(A-1) of 5 to 10 percent (weight) in benzene, at a temperature of less than 20 0 C. The mechanism of uranium extraction was discussed on the basis of the resluts obtained. (author)

High-temperature, Knudsen cell-mass spectroscopic studies on lanthanum oxide/uranium dioxide solid solutions

International Nuclear Information System (INIS)

Sunder, S.; McEachern, R.; LeBlanc, J.C.

2001-01-01

Knudsen cell-mass spectroscopic experiments were carried out with lanthanum oxide/uranium oxide solid solutions (1%, 2% and 5% (metal at.% basis)) to assess the volatilization characteristics of rare earths present in irradiated nuclear fuel. The oxidation state of each sample used was conditioned to the 'uranium dioxide stage' by heating in the Knudsen cell under an atmosphere of 10% CO 2 in CO. The mass spectra were analyzed to obtain the vapour pressures of the lanthanum and uranium species. It was found that the vapour pressure of lanthanum oxide follows Henry's law, i.e., its value is directly proportional to its concentration in the solid phase. Also, the vapour pressure of lanthanum oxide over the solid solution, after correction for its concentration in the solid phase, is similar to that of uranium dioxide. (authors)

Thermodynamic properties of uranium in gallium–aluminium based alloys

International Nuclear Information System (INIS)

Volkovich, V.A.; Maltsev, D.S.; Yamshchikov, L.F.; Chukin, A.V.; Smolenski, V.V.; Novoselova, A.V.; Osipenko, A.G.

2015-01-01

Activity, activity coefficients and solubility of uranium was determined in gallium-aluminium alloys containing 1.6 (eutectic), 5 and 20 wt.% aluminium. Additionally, activity of uranium was determined in aluminium and Ga–Al alloys containing 0.014–20 wt.% Al. Experiments were performed up to 1073 K. Intermetallic compounds formed in the alloys were characterized by X-ray diffraction. Partial and excess thermodynamic functions of U in the studied alloys were calculated. - Highlights: • Thermodynamics of uranium is determined in Ga–Al alloys of various compositions. • Uranium in the mixed alloys interacts with both components, Ga and Al. • Interaction of U with Al increases with decreasing temperature. • Activity and solubility of uranium depend on Al content in Ga–Al alloys.

Thermodynamic properties of uranium in gallium–aluminium based alloys

Energy Technology Data Exchange (ETDEWEB)

Volkovich, V.A., E-mail: v.a.volkovich@urfu.ru [Department of Rare Metals and Nanomaterials, Institute of Physics and Technology, Ural Federal University, Ekaterinburg, 620002 (Russian Federation); Maltsev, D.S.; Yamshchikov, L.F. [Department of Rare Metals and Nanomaterials, Institute of Physics and Technology, Ural Federal University, Ekaterinburg, 620002 (Russian Federation); Chukin, A.V. [Department of Theoretical Physics and Applied Mathematics, Institute of Physics and Technology, Ural Federal University, Ekaterinburg, 620002 (Russian Federation); Smolenski, V.V.; Novoselova, A.V. [Institute of High-Temperature Electrochemistry UD RAS, Ekaterinburg, 620137 (Russian Federation); Osipenko, A.G. [JSC “State Scientific Centre - Research Institute of Atomic Reactors”, Dimitrovgrad, 433510 (Russian Federation)

2015-10-15

Activity, activity coefficients and solubility of uranium was determined in gallium-aluminium alloys containing 1.6 (eutectic), 5 and 20 wt.% aluminium. Additionally, activity of uranium was determined in aluminium and Ga–Al alloys containing 0.014–20 wt.% Al. Experiments were performed up to 1073 K. Intermetallic compounds formed in the alloys were characterized by X-ray diffraction. Partial and excess thermodynamic functions of U in the studied alloys were calculated. - Highlights: • Thermodynamics of uranium is determined in Ga–Al alloys of various compositions. • Uranium in the mixed alloys interacts with both components, Ga and Al. • Interaction of U with Al increases with decreasing temperature. • Activity and solubility of uranium depend on Al content in Ga–Al alloys.

Influence of the temperature in the uranium (Vi) sorption in zirconium diphosphate; Influencia de la temperatura en la sorcion de uranio (VI) en difosfato de circonio

Energy Technology Data Exchange (ETDEWEB)

Garcia G, N.; Solis, D. [Universidad Autonoma del Estado de Mexico, Facultad de Quimica, Paseo Colon y Paseo Tollocan, 50120 Toluca, Estado de Mexico (Mexico); Ordonez R, E., E-mail: nidgg@yahoo.com.mx [ININ, Departamento de Quimica, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

2012-10-15

In the present work was evaluated the uranium (Vi) sorption at 10, 20, 30, 40 and 60 C on the zirconium diphosphate (ZrP{sub 2}O{sub 7}). They were carried out kinetic and isotherms using the method by lots, these will allow to fix the sorption time (kinetic) and to explain the behavior of this sorption in different ph conditions and temperature (isotherm). The quantity of retained uranium in the surface was quantified by means of the fluorescence technique. (Author)

Comparison of the Spatiotemporal Variability of Temperature, Precipitation, and Maximum Daily Spring Flows in Two Watersheds in Quebec Characterized by Different Land Use

Directory of Open Access Journals (Sweden)

Ali A. Assani

2016-01-01

Full Text Available We compared the spatiotemporal variability of temperatures and precipitation with that of the magnitude and timing of maximum daily spring flows in the geographically adjacent L’Assomption River (agricultural and Matawin River (forested watersheds during the period from 1932 to 2013. With regard to spatial variability, fall, winter, and spring temperatures as well as total precipitation are higher in the agricultural watershed than in the forested one. The magnitude of maximum daily spring flows is also higher in the first watershed as compared with the second, owing to substantial runoff, given that the amount of snow that gives rise to these flows is not significantly different in the two watersheds. These flows occur early in the season in the agricultural watershed because of the relatively high temperatures. With regard to temporal variability, minimum temperatures increased over time in both watersheds. Maximum temperatures in the fall only increased in the agricultural watershed. The amount of spring rain increased over time in both watersheds, whereas total precipitation increased significantly in the agricultural watershed only. However, the amount of snow decreased in the forested watershed. The magnitude of maximum daily spring flows increased over time in the forested watershed.

Can we predict uranium bioavailability based on soil parameters? Part 1: effect of soil parameters on soil solution uranium concentration.

Science.gov (United States)

Vandenhove, H; Van Hees, M; Wouters, K; Wannijn, J

2007-01-01

Present study aims to quantify the influence of soil parameters on soil solution uranium concentration for (238)U spiked soils. Eighteen soils collected under pasture were selected such that they covered a wide range for those parameters hypothesised as being potentially important in determining U sorption. Maximum soil solution uranium concentrations were observed at alkaline pH, high inorganic carbon content and low cation exchange capacity, organic matter content, clay content, amorphous Fe and phosphate levels. Except for the significant correlation between the solid-liquid distribution coefficients (K(d), L kg(-1)) and the organic matter content (R(2)=0.70) and amorphous Fe content (R(2)=0.63), there was no single soil parameter significantly explaining the soil solution uranium concentration (which varied 100-fold). Above pH=6, log(K(d)) was linearly related with pH [log(K(d))=-1.18 pH+10.8, R(2)=0.65]. Multiple linear regression analysis did result in improved predictions of the soil solution uranium concentration but the model was complex.

Elemental imaging of kidneys of adult rats exposed to uranium acetate

Energy Technology Data Exchange (ETDEWEB)

Homma-Takeda, S. [Research Center for Radiation Protection, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba 263-8555 (Japan)], E-mail: shino_ht@nirs.go.jp; Terada, Y. [Japan Synchrotron Radiation Research Institute, Mikazuki, Hyogo 679-5198 (Japan); Nakata, A.; Sahoo, S.K.; Yoshida, S. [Research Center for Radiation Protection, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba 263-8555 (Japan); Ueno, S. [School of Veterinary Medicine, Kitasato University, Towada, Aomori 034-8628 (Japan); Inoue, M. [Research Center for Radiation Protection, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba 263-8555 (Japan); Iso, H.; Ishikawa, T.; Konishi, T.; Imaseki, H. [Fundamental Technology Center, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba 263-8555 (Japan); Shimada, Y. [Research Center for Radiation Protection, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage-ku, Chiba 263-8555 (Japan)

2009-06-15

Concern about the toxicity of depleted uranium for military use has increased recently. Renal toxicity is the hallmark effect of uranium exposure. However, the dynamics and distribution of uranium in the kidney are not well understood. Here, we determined the precise distribution of uranium and essential elements in the rat kidney using microbeam scanning particle-induced X-ray emission (micro-PIXE) and synchrotron radiation X-ray fluorescence (SR-XRF). Uranium accumulation in the rat kidney reached a maximum at 1 day after the subcutaneous (s.c.) administration of 2 mg U/kg of uranium acetate and then gradually decreased. At 3 h after administration, uranium was distributed mainly in the proximal tubules of the inner zone of the cortex and in the outer stripe of the outer medulla, and absorbed by the proximal tubule epithelium. Iron was localized more in the inside of the outer medulla than uranium, while phosphorus, potassium, sulfur and zinc were equally distributed in the cortex and the outer stripe of the outer medulla. At 3 days after administration, the number of apoptotic cells increased and cells were lost from the proximal tubules. Uranium was detectable mainly in the outer stripe of the outer medulla at 15 days, suggesting that the renal distribution of uranium is site-selective and causes site-specific renal lesions.

Kinetics of the reduction of uranium oxide catalysts

International Nuclear Information System (INIS)

Heynen, H.W.G.; Camp-van Berkel, M.M.; Bann, H.S. van der

1977-01-01

The reduction of uranium oxide and uranium oxide on alumina catalysts by ethylbenzene and by hydrogen has been studied in a thermobalance. Ethylbenzene mole fractions between 0.0026 and 0.052 and hydrogen mole fractions between 0.1 and 0.6 were applied at temperatures of 425--530 0 C. During the reduction the uranium oxides are converted into UO 2 . The rate of reduction of pure uranium oxide appears to be constant in the composition region UO/sub 2.6/-UO/sub 2.25/. The extent of this region is independent of the concentration of the reducing agents and of the reaction temperature. The constant rate is explained in terms of a constant oxygen pressure which is in equilibrium with the two solid phases, U 3 O/sub 8-x/ and U 4 O 9 . The reduction rate is first order in hydrogen and zero order in ethylbenzene with activation energies of 120 and 190 kJ mol -1 , respectively. Oxygen diffusion through the lattice is probably not rate limiting. The reduction behavior of uranium oxide on alumina is different from that of pure uranium oxide; the rate of reduction continuously decreases with increasing degree of reduction. An explanation for this behavior has been given by visualizing this catalyst as a set of isolated uranium oxide crystallites with a relative wide variation of diameters, in an alumina matrix. At the beginning of the reduction, carbon dioxide and water are the only reaction products. Thereafter, benzene is found as well and, finally, at U/O ratios below 2.25, styrene also appears in the reactor outlet

Sorption of uranium anionic species from aqueous solutions on HDTMA-bentonite Jelsovy potok

International Nuclear Information System (INIS)

Krajnak, A.; Viglasova, E.; Galambos, M.; Rosskopfova, O.

2014-01-01

Bentonite deposit Jelsovy potok in Slovakia has great potential for use as a engineering barrier in the multi-barrier system of deep geological repository. In this paper, HDTMA-modified bentonite J15m from Slovak bentonite Jelsovy potok was prepared and its sorption properties (sorption isotherms, kinetics) towards anionic uranium species was investigated. The removal of uranium anionic species from aqueous solutions (initial concentration: 10-1,000 mg/L) by J15m was studied in the absence of background electrolytes at initial pH range (pH init ) 8.5; 9.5; 10.5. The amount of the sorbed U was determined spectrophotometrically using the Arsenazo III method. The maximum uptake capacity observed was 31.35 (mg/g) at 298 K. Experimental results were analysed by the Langmuir, Freundlich Dubinin-Redushkevich and Tempkin isotherm. The kinetics of adsorption of U(VI) ions was also discussed using the pseudo-first-order and the pseudo-second-order at three different temperatures. The activation energy of the sorption for J15m was calculated as 23.534 kJ·mol -1 . (authors)

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

Sintering of uranium oxide of high specific surface area

International Nuclear Information System (INIS)

Bel, Alain; Francois, Bernard; Delmas, Roger; Caillat, Roger

1959-01-01

The extent to which a uranium oxide powder deriving from ammonium uranate or uranium peroxide lends itself to the sintering process depends largely on its specific surface area. When this is greater than 5 m 2 / g there is an optimum temperature for sintering in hydrogen. This temperature becomes less as the specific area of the powder is greater. Reprint of a paper published in Comptes rendus des seances de l'Academie des Sciences, t. 249, p. 1045-1047, sitting of 21 September 1959 [fr

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)

Removal of uranium from ammonium nitrate solution by nanofiltration

Energy Technology Data Exchange (ETDEWEB)

Wang, Runci; Yuan, Zhongwei; Yan, Taihong; Zheng, Weifang [China Institute of Atomic Energy, Beijing (China). Dept. of Radiochemistry

2017-07-01

Two types of nanofiltration membranes were tested to remove uranium dissolved in ammonium nitrate solution, and the influence of operating parameters as transmembrane pressure, tangential velocity and feed temperature was investigated. Experimental results showed NF270 membrane can reject more than 96% uranium and allow most (90% min) ammonium nitrate solution passed by, and with a permeate flux of 60 L/(m{sup 2}.h). Nanofiltration seems to be a promising technology for the removal of uranium and recovery of ammonium nitrate simultaneously.

Characterisation and dissolution studies on the uranium pyrochlore mineral betafite (Ca,U)_2(Nb,Ti,Ta)_2O_7

International Nuclear Information System (INIS)

McMaster, S.; Ram, R.; Tardio, J.; Bhargava, S.

2014-01-01

conditions: [H_2SO_4] between 0 and 100 g/L, [Fe_T_O_T] between 0 and 12 g/L, Redox potential (Fe"3"+:Fe"2"+ Ratio), between 1:0 to 0:1, Temperature (35-95°C) and crystallinity (pre heat treated and heat treated). The results of the dissolution studies showed similar trends between the 3 samples studied. Increasing the temperature had the most significant effect on dissolution. Similar trends between the samples were seen with the effect of [Fe_T_O_T] and Redox potential. All studies completed looking at these two parameters showed very minor changes in dissolution concentration as these parameters were changed. The maximum uranium dissolution for BAM, BMM and BSC was 70, 34 and 45% respectively. This was achieved with; 3g/L Iron (100% as Fe"3"+); 50g/L H_2SO_4; 95°C temperature after 24 hrs. (author)

Thermal simulation of the magnesium thermal of metallic uranium reduction

International Nuclear Information System (INIS)

Borges, W.A.; Saliba-Silva, A.M.

2008-01-01

Metallic uranium production is vital to fabricate fuel elements for nuclear research reactors and to produce radioisotopes and radiopharmaceuticals. Metallic uranium is got via magnesiothermal reduction of UF 4 . This reaction is carried out inside a closed graphite crucible inserted in a metallic reactor adequately sealed without any outside contact. The assembled set is gradually heated up inside a pit furnace up to reach the reaction ignition temperature (between 600-650 deg C). The optimization of the reactive system depends on the mathematical modeling using simulation by finite elements and computational calculation with specialized programs. In this way, the reactants' thermal behavior is forecast until they reach the ignition temperature. The optimization of the uranium production reaction is based on minimization of thermal losses using better the exo thermal reaction heat. As lower the thermal losses, as higher would be the heat amount to raise the temperature of reaction products. This promotes the adequate melting of uranium and slag, so allowing better metal/slag separation with higher metallic yield. This work shows how the mathematical simulation is made and supplies some preliminary results. (author)

Organic matter in uranium concentration during ancient bed oxidation of carboniferons sediments

International Nuclear Information System (INIS)

Kruglova, V.G.; Uspenskij, V.A.; Dement'ev, P.K.; Kochenov, A.V.

1984-01-01

Changes in the organic matter accompanying the process of epigenetic ore formation are studied using the example of a deposit localized in carboniferous molasse strata of the Cretaceous period. Peculiarities of the organic matter as the main mineralization agent are studied by a complex of physical and themical methods. A distinct relationship between the uranium concentration and the degree of organic matter oxigenation is a most characteristic feature of the ore localization, however, there is no direct correlation between the contents of uranium and organic matter in ores. Uranium minerallzation was accumulated during infiltration of acid uraniferous.waters into grey stratum in the process of the bed oxidation zone formation oxidizing. Brown coal matter possessing a maximum adsorbability, as compared to other sedimentary rocks, apprared to be the uranium precipitator. The adsorption was accompanie by the formation of proper uranium minerals (coffinite, pitchblende) due to uranium reduction by oxidizing organic matter. Thus, the oxidative epigenesis was an are-forming process with the uranium concentration on organic matter proportionally to oxidation of the latter

Study on depleted uranium at the airplane accident in Bijlmermeer, Amsterdam, Netherlands

International Nuclear Information System (INIS)

Veltkamp, A.C.; Van Hienen, J.F.A.

1998-09-01

The El Al airplane, which crashed in the urban area Bijlmermeer in Amsterdam, Netherlands, October 4th, 1992, contained balance weights of depleted uranium. Part of the balance weights has not been found after the disaster and its not sure what happened with the lost part. One of the options is that the uranium atomized during or after the fire. To clarify this the Dutch Civil Aviation Authority (RLD) ordered the Netherlands Energy Research Foundation (ECN) to study the fore-mentioned option on the basis of the following questions: (1) at which temperature will depleted uranium atomize and thus be released into the air?; (2) at which temperature will depleted uranium burn?; and (3) what is the chance that depleted uranium will atomize under the conditions as they occurred during the aircraft accident in the Bijlmermeer? The overall impression is that during the fire little if any uranium oxide has been released into the air. Because of lack of knowledge about the actual conditions, partial or complete oxidation can not be excluded with cast-iron certainty. 16 refs

Development of an On-Line Uranium Enrichment Monitor

International Nuclear Information System (INIS)

Xuesheng, L.; Guorong, L.; Yonggang, Z.; Xueyuan, H. X.-Y.

2015-01-01

An on-line enrichment monitor was developed to measure the enrichment of UF6 flowing through the processing pipes in centrifuge uranium enrichment plant. A NaI(Tl) detector was used to measure the count rates of the 186 keV gamma ray emitted from 235U, and the total quantity of uranium was determined from thermodynamic characteristics of gaseous uranium hexafluoride. The results show that the maximum relative standard deviation is less than 1% when the measurement time is 120 s or more and the pressure is more than 2 kPa in the measurement chamber. There are two working models for the monitor. The monitor works normally in the continuous model, When the gas's pressure in the pipe fluctuates greatly, it can work in the intermittent model, and the measurement result is very well. The background of the monitor can be measured automatically periodically. It can control automatically electromagnetic valves open and close, so as to change the gas's quantity in the chamber. It is a kind of unattended and remote monitor, all of data can be transfer to central control room. It should be effective for nuclear materials accountability verifications and materials balance verification at uranium enrichment plant by using the monitor to monitor Uranium enrichment of gaseous uranium hexafluoride in the output end of cascade continuously. (author)

Recent developments concerning French fuel elements used in natural uranium - graphite - CO{sub 2} reactor systems; Developpements recents des elements combustibles francais de la filiere uranium naturel - graphite - CO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Salesse, M; Stohr, J A; Jeanpierre, G [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1964-07-01

internal can of the annular element, has necessitated very much research work. - the exact temperature drop at the contact between the uranium and the can, and the strength of the lower end of the cartridge are points which are increasingly crucial in the case of the annular element. All in all the annular element thus calls for a great research effort. This effort is justified by the big step forwards in which it will result in the case of the EDF reactors thanks to its high specific power and to the high weight of uranium in each cartridge. (authors) [French] La politique choisie en France pour le developpement des elements combustibles destines aux reacteurs de l'Electricite de France, consiste a chercher, pour chaque pile nouvelle, a beneficier au maximum des progres techniques les plus recents en etudiant chaque fois un nouvel element combustible permettant une puissance par canal aussi elevee que possible. Les derniers elements combustibles ainsi etudies par le Commissariat a l'Energie Atomique sont de deux types differents: un element a tube d'uranium ferme aux deux extremites et refroidi exterieurement (ce type d'element, retenu pour les reacteurs EDF 2, EDF 3 et EDF 4 permet des puissances specifiques maximum de l'ordre de 6 MW/t). Un element a tube d'uranium ouvert, refroidi interieurement et exterieurement, appele clemont annulaire et dont on etudie la possibilite pour EDF5. Un tel element peut permettre des puissances specifiques superieures a 12 MW/t. Ces deux types d'elements possedent des caracteristiques communes: la gaine, pour le refroidissement externe, comporte des ailettes en chevron. Ce type de profil, qui a recu recemment des ameliorations notables augmentant son efficacite thermique, a l'avantage important d'eviter les vibrations de cartouche mais a pose des problemes technologiques de tenue au cyclage thermique qui ont necessite une etude approfondie. les cartouches sont placees a l'interieur de chemise en graphite, ce qui limite les efforts

Distribution of uranium in marine sediments

International Nuclear Information System (INIS)

Ordonez R, E.; Ramirez T, J.J.; Lopez M, J.; Aspiazu, J.; Ruiz F, A.C.; Valero C, N.

2008-01-01

The marine sediments obtained by means of a sampling nucleus in the Gulf of Tehuantepec, Mexico, they have been object of crystallographic and morphological characterization. The PIXE analysis of some samples in study is shown. The normal methodology to carry out the alpha spectroscopy indicates that the sample should be dissolved, but due to the nature of the marine sediments, it thinks about the necessity to make a fractional separation of the sample components. In each stratum of the profile it separates the organic part and the mineral to recover the uranium. It was observed that in the organic phase, the uranium is in two oxidation states (IV and Vl), being necessary the radiochemical separation with a liquid/liquid column chromatographic that uses the di-2-ethyl hexyl phosphoric acid as stationary phase. The uranium compounds extracts are electrodeposited in fine layers on stainless steel disks to carry out the analysis by alpha spectroscopy. The spectroscopic analysis of the uranium indicates us that for each stratum one has a difference marked in the quotient of activities of 234 U/ 238 U that depends on the nature of the studied fraction. These results give us a clear idea about how it is presented the effect of the uranium migration and other radioelements in the biosphere, with what we can determine which are the conditions in that these have their maximum mobility and to know their diffusion patterns in the different media studied. (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

Methodology of simultaneous analysis of Uranium and Thorium by nuclear and atomic techniques. Application to the Uranium and Thorium dosing in mineralogic samples

International Nuclear Information System (INIS)

Fakhi, S.

1988-01-01

This work concerns essentially the potential applications of 100 kW nuclear reactor of Strasbourg Nuclear Research Centre to neutron activation analysis of Uranium and Thorium. The Uranium dosing has been made using: 239-U, 239-Np, fission products or delayed neutrons. Thorium has been showed up by means of 233-Th or 233-Pa. The 239-U and 233-Th detection leads to a rapid and non-destructive analysis of Uranium and Thorium. The maximum sensitivity is of 78 ng for Uranium and of 160 ng for Thorium. The Uranium and Thorium dosing based on 239-Np and 233-Pa detection needs chemical selective separations for each of these radionuclides. The liquid-liquid extraction has permitted to elaborate rapid and quantitative separation methods. The sensitivities of the analysis after extraction reach 30 ng for Uranium and 50 ng for Thorium. The fission products separation study has allowed to elaborate the La, Ce and Nd extractions and its application to the Uranium dosing gives satisfying results. A rapid dosing method with a sensitivity of 0.35 microgramme has been elaborated with the help of delayed neutrons measurement. These different methods have been applied to the Uranium and Thorium dosing in samples coming from Oklo mine in Gabon. The analyses of these samples by atomic absorption spectroscopy and by the proton induced X-ray emission (PIXE) method confirm that the neutron activation analysis methods are reliable. 37 figs., 14 tabs., 50 refs

Preparation and Purification of natural uranium metal by Iodine method

International Nuclear Information System (INIS)

Taies, J.A.

2008-01-01

In this work ,glass-metal apparatus was designed and manufactured which used for preparing a high purity uranium.The reaction is simply take place between iodine vapour and uranium metal at 500C in closed system to form uranium tetra iodide which is decomposed on hot wire at high temperature around 1100C.Also another apparatus was made from Glass and used for preparing a high purity of UI 4 more than 99.9%purity

Extended Kalman Filtering to estimate temperature and irradiation for maximum power point tracking of a photovoltaic module

International Nuclear Information System (INIS)

Docimo, D.J.; Ghanaatpishe, M.; Mamun, A.

2017-01-01

This paper develops an algorithm for estimating photovoltaic (PV) module temperature and effective irradiation level. The power output of a PV system depends directly on both of these states. Estimating the temperature and irradiation allows for improved state-based control methods while eliminating the need of additional sensors. Thermal models and irradiation estimators have been developed in the literature, but none incorporate feedback for estimation. This paper outlines an Extended Kalman Filter for temperature and irradiation estimation. These estimates are, in turn, used within a novel state-based controller that tracks the maximum power point of the PV system. Simulation results indicate this state-based controller provides up to an 8.5% increase in energy produced per day as compared to an impedance matching controller. A sensitivity analysis is provided to examine the impact state estimate errors have on the ability to find the optimal operating point of the PV system. - Highlights: • Developed a temperature and irradiation estimator for photovoltaic systems. • Designed an Extended Kalman Filter to handle model and measurement uncertainty. • Developed a state-based controller for maximum power point tracking (MPPT). • Validated combined estimator/controller algorithm for different weather conditions. • Algorithm increases energy captured up to 8.5% over traditional MPPT algorithms.

Translocation of uranium from water to foodstuff while cooking.

Science.gov (United States)

Krishnapriya, K C; Baksi, Ananya; Chaudhari, Swathi; Gupta, Soujit Sen; Pradeep, T

2015-10-30

The present work report the unusual uranium uptake by foodstuff, especially those rich in carbohydrates like rice when they are cooked in water, contaminated with uranium. The major staple diet in South Asia, rice, was chosen to study its interaction with UO2(2+), the active uranium species in water, using inductively coupled plasma mass spectrometry. Highest uptake limit was checked by cooking rice at very high uranium concentration and it was found to be good scavenger of uranium. To gain insight into the mechanism of uptake, direct interaction of UO2(2+) with monosaccharides was also studied, using electrospray ionization mass spectrometry taking mannose as a model. The studies have been done with dissolved uranium salt, uranyl nitrate hexahydrate (UO2(NO3)2·6H2O), as well as the leachate of a stable oxide of uranium, UO2(s), both of which exist as UO2(2+) in water. Among the eight different rice varieties investigated, Karnataka Ponni showed the maximum uranium uptake whereas unpolished Basmati rice showed the minimum. Interaction with other foodstuffs (potato, carrot, peas, kidney beans and lentils) with and without NaCl affected the extent of chemical interaction but was not consistent with the carbohydrate content. Uranium interaction with D-mannose monitored through ESI-MS, under optimized instrumental parameters, identified the peaks corresponding to uranyl adduct with mannose monomer, dimer and trimer and the species were confirmed by MS/MS studies. The product ion mass spectra showed peaks illustrating water loss from the parent ion as the collision energy was increased, an evidence for the strong interaction of uranium with mannose. This study would constitute the essential background for understanding interaction of uranium with various foods. Extension of this work would involve identification of foodstuff as green heavy metal scavengers. Copyright © 2015. Published by Elsevier B.V.

General trends in the use of uranium in the nuclear industry; Tendances generales d'emploi de l'uranium dans les industries nucleaires

Energy Technology Data Exchange (ETDEWEB)

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

1960-07-01

It can be seen from a consideration of the development of the military and civil needs for uranium that, in the long run, the main outlet for the metal will be provided by its industrial applications. The technical uncertainties concerning the best method of producing atomic energy are still numerous and in fact reflect the hesitation in choosing one of two classes of fuel: that based on the metal and that based on the oxide. Four main factors should influence the choice: - the neutron reactivity and the enrichment of the uranium; - the operating temperature; - the resistance to radiation effects; - the chemical stability; but in actual fact, when the choice for a particular use has to be made, it will be another type of factor, such as the cost price, and weight and space considerations which will determine the choice of either metallic uranium or uranium oxide reactors. (author) [French] D'apres le developpement des besoins militaires ou civils en uranium, on voit que les usages industriels de ce metal constituent, a long terme, le debouche essentiel. Les incertitudes techniques, sur le procede optimum pour faire de l'energie nucleaire, restent nombreuses, et se traduisent finalement par une hesitation entre deux grandes classes de combustibles: ceux a base de metal et ceux a base d'oxyde: la preference a l'une ou l'autre de ces deux categories doit s'inspirer de quatre considerations: - la reactivite neutronique et l'enrichissement de l'uranium; - la temperature de fonctionnement; - la resistance aux effets du rayonnement; - la stabilite chimique; mais en definitive, lorsqu'il s'agira d'une application determinee, ce seront des considerations d'un autre ordre, comme le prix de revient, le poids et l'encombrement, qui determineront le choix entre piles a uranium metallique et piles a oxyde d'uranium. (auteur)

Contribution to the study of point defects in uranium {alpha}; Contribution a l'etude des defauts ponctuels dans l'uranium {alpha}

Energy Technology Data Exchange (ETDEWEB)

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

1967-07-01

Uranium quenched from temperatures as low as 100 K shows an important increase in resistivity which disappears after annealing between 4.2 K and 41 K. This phenomenon is explained by a cold-work of the metal due to the rapid traversing of the temperature region where the lattice parameters exhibit an important and anisotropic increase. The annealing occurs in two stages (4.2 K - 26 K - 41 K). Purity of samples has an influence on the phenomenon. Model proposed is confirmed by the comparison with some experiments of annealing of defects created by irradiation of uranium at very low temperatures. Vacancies have been quenched in the metal from temperatures around 650 C (limit of the {alpha} phase). The formation energy so found is E{sub F} = 0. 5 {+-} 0.15 eV. The annealing out of the induced resistivity happens in two stages (300-390; 420-560 C). (authors) [French] La trempe de l'uranium dans l'helium liquide depuis des temperatures aussi basses que 100 K entraine une augmentation de resistivite qui disparait par recuit entre 4.2 K et 41 K. Ce phenomene est interprete comme un ecrouissage du metal provoque par la traversee rapide d'une region ou les parametres cristallins varient beaucoup et de facon anisotrope. Le recuit se fait en deux stades (4.2 K - 26 K - 41 K). La purete des echantillons a une influence sur le phenomene. Le modele propose a ete verifie par comparaison avec des experiences de recuit de defauts crees par irradiation de l'uranium a tres basse temperature. Des lacunes ont ete retenues a l'etat metastable par trempe du metal depuis des temperatures voisines de 650 C (limite de la phase {alpha}). L'energie de formation trouvee est E{sub F} = 0.5 {+-} 0.15 eV. La guerison se fait en deux stades (300-390 C; 420-560 C). (auteurs)

Desorption of uranium from titanium-activated carbon composite adsorbent with acidic eluent, 1

International Nuclear Information System (INIS)

Hirotsu, Takahiro; Fujii, Ayako; Sakane, Kohji; Katoh, Shunsaku; Sugasaka, Kazuhiko

1984-01-01

An investigation was carried out on the desorption of uranium from titanium-activated carbon composite adsorbent with acidic eluent by the batch process. The rate of desorption of uranium with acidic eluent depended on temperature, showing an increase as the temperature was raised. But the rate of desorption with acidic eluent was less dependent on temperature than that obtained when mixed eluent of sodium carbonate-sodium hydrogencarbonate was used. The rate of desorption of uranium did not vary in the range of concentration from 0.3 to 0.5 N, and the rate of desorption with sulfuric acid was slightly higher than that obtained when hydrochloric acid was used. The amount of dissolved titanium decreased as the ratio of adsorbent to eluent (RAE) was increased. At RAE of 10 %, the percentage of dissolved titanium (DTI) was below 0.38 % with sulfuric acid, below 0.7 % with hydrochloric acid. These values were found to be higher than the ones with the carbonate eluent. The elements except uranium, which were adsorbed on the adsorbent, were eluted simultaneously with acidic eluent. The regeneration of the adsorbent after desorption, therefore, was found to be unnecessary. In a repeated test of adsorption-desorption treatment up to five times, the percentage of uranium adsorbed from natural sea water was approximately constant of 85 %. From these results, the application of column process to the desorption of uranium with acidic eluent at room temperature was proposed to be feasible. (author)

Desorption of uranium from titanium-activated carbon composite adsorbent with acidic eluent, (1)

International Nuclear Information System (INIS)

Hirotsu, Takahiro; Fujii, Ayako; Sakane, Kohji; Katoh, Shunsaku; Sugasaka, Kazuhiko

1983-01-01

An investigation was carried out on the desorption of uranium from titanium-activated carbon composite adsorbent with acidic eluent by the batch process. The rate of desorption of uranium with acidic eluent depended on temperature, showing an increase as the temperature was raised. But the rate of desorption with acidic eluent was less dependent on temperature than that obtained when mixed eluent of sodium carbonate-sodium hydrogencarbonate was used. The difference of the rate of desorption of uranium in the range of concentration from 0.3 to 0.5N was not found, and the rate of desorption with sulfuric acid was slightly higher than that obtained when hydrochloric acid was used. The amount of dissolved titanium decreased as the ratio of adsorbent to eluent (RAE) was increased. At RAE of 10%, the percentage of dissolved titanium (DTI) was below 0.38% with sulfuric acid, below 0.7% with hydrochloric acid. These values were found to be higher than the ones with the carbonate eluent. The elements except uranium, which were adsorbed on the adsorbent, were eluted simultaneously with acidic eluent. The regeneration of the adsorbent after desorption, therefore, was found to be unnecessary. In a repeated test of adsorption-desorption treatment up to five times, the percentage of uranium adsorbed from natural sea water was approximately constant of 85%. From these results, the application of column process to the desorption of uranium with acidic eluent at room temperature was proposed to be feasible. (author)

Calculation of the fissile mass of a graphite moderated critical assembly using 93% enriched uranium

International Nuclear Information System (INIS)

Correa, F.; Marzo, M.A.S.; Collussi, I.; Ferreira, A.C.A.

1976-01-01

The critical mass of uranium has been calculated for a graphite moderated set fueled with 93% enriched uranium to be mounted on the Instituto de Energia Atomica split table Zero Power Reactor. The core composition was optimized to permit the maximum number of configurations to be studied. Analysis of three core compositions shows that 8 Kg of uranium enriched to 93% - U-235 (by weight) and 100 Kg of thorium would be sufficient for criticality experiments [pt

Removal of uranium from simulated fly ash by chloride volatilization method

International Nuclear Information System (INIS)

Nobuaki, Sato; Yoshikatsu, Tochigi; Toshiki, Fukui; Takeo, Fujino

2003-01-01

Fly ash is generated from LWR nuclear power plant as a low-level waste, which is contaminated with a small amount of radioactive materials, composed mainly of uranium oxide. The constituents of the fly ash are similar to those of the ore; the major components of the ash are oxides of silicon, aluminum, sodium, magnesium, zinc, iron sodium and uranium. In this study, removal of uranium from the simulated fly ash, of which composition was U 3 O 8 : 10, CaO:25, SiO 2 : 25, Al 2 O 3 : 20, MgO: 10, ZnO:5, Fe 2 O 3 : 3 and Na 2 CO 3 : 2 wt%, by chloride volatilization method was examined. The simulated fly ash was chlorinated by the same manner as the dry way processing for the ore; namely, the ash was heated in a flow of chlorine in the presence of carbon at high temperatures. In the case of volatilization of uranium from U 3 O 8 and a simulated fly ash by chlorination using chlorine and carbon, it was seen that uranium of both samples showed similar volatilization behaviour: The volatilization ratio of uranium (VU) increased with increasing temperature from 800 to 1100 C. The VU value attained 99.9% at 1100 C. Iron, silicon and zinc showed similar behaviour to uranium, namely, they vaporized completely. The volatilization ratio of aluminum, magnesium and sodium were still high in a range 80-90%. The volatilization ratio of calcium was ∼40% under the same chlorination condition, though it changed to chloride. For recovery of uranium from fly ash by chlorination using chlorine in the presence of carbon, high volatilization ratio of uranium can be achieved at high temperatures. Volatilization ratio of other components also increases, which decreases the amount of decontaminated residue resulting in the reducing of decontamination effect. Selection of heating condition is important. (author)

Salt evaporation behaviors of uranium deposits from an electrorefiner

International Nuclear Information System (INIS)

Sung Bin Park; Dong Wook Cho; Gyu Hwan Oh; Sung Chan Hwang; Young Ho Kang; Hansoo Lee; Eung Ho Kim; Seong-Won Park; Jong Hyeon Lee

2010-01-01

From an electrorefining process, uranium deposits were recovered at the solid cathode of an electrorefining system. The uranium deposits from the electrorefiner contained about 30-40 wt% salts. In order to recover pure uranium and transform it into metal ingots, these salts have to be removed. A salt distiller was adapted for a salt evaporation. A batch operation for the salt removal was carried out by a heating and a vacuum evaporation. The operational conditions were a 700-1,000 deg C hold temperature and less than a 1 Torr under Argon atmosphere, respectively. The behaviors of the salt evaporations were investigated by focusing on the effects of the pressure and the holding temperature for the salt distillation. The removal efficiencies of the salts were obtained with regard to the operational conditions. The experimental results of the salt evaporations were evaluated by using the Hertz-Langmuir relation. The effective evaporation coefficients of this relation were obtained with regards to the vacuum pressures and the hold temperatures. The higher the vacuum pressure and the higher the holding temperature were, the higher the removal efficiencies of the salts were. (author)

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

International Nuclear Information System (INIS)

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

1993-01-01

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

Uranium extraction from sulfuric acid solution using anion exchange resin

International Nuclear Information System (INIS)

Sheta, M. E.; Abdel Aal, M. M.; Kandil, A. T.

2012-12-01

Uranium is currently recovered from sulfuric acid leach liquor using anion exchange resin as Amberlite IRA 402 (CT). This technology is based on fact that, uranium exists as anionic complexes. This takes place by controlling the pH of the solution, agitation time, temperature and resin to solution ratio (R/S). In this work, batch stirrer tank used for uranium extraction from sulfate medium and after extraction, elution process was done using 1M NaCl solution. After extraction and elution process, the resin was separated from the system and uranium was determined in the solution. (Author)

Possible uranium sources of Streltsovsky uranium ore field

International Nuclear Information System (INIS)

Zhang Lisheng

2005-01-01

The uranium deposit of the Late Jurassic Streltsovaky caldera in Transbaikalia of Russia is the largest uranium field associated with volcanics in the world, its uranium reserves are 280 000 t U, and it is the largest uranium resources in Russia. About one third of the caldera stratigraphic pile consists of strongly-altered rhyolites. Uranium resources of the Streltsovsky caldera are much larger than any other volcanic-related uranium districts in the world. Besides, the efficiency of hydrothermal alteration, uranium resources appear to result from the juxtaposition of two major uranium sources; highly fractionated peralkaline rhyolites of Jurassic age in the caldera, and U-rich subalkaline granites of Variscan age in the basement in which the major uranium-bearing accessory minerals were metamict at the time of the hydrothermal ore formation. (authors)

Ingot formation using uranium dendrites recovered by electrolysis in LiCl-KCl-PuCl3-UCl3 melt

International Nuclear Information System (INIS)

Mineo Fukushima; Akira Nakayoshi; Shinichi Kitawaki; Masaki Kurata; Noboru Yahagi

2008-01-01

Products on solid cathodes recovered by the metal pyrochemical processing were processed to obtain uranium ingot. Studies on process conditions of uranium formation, assay recovered uranium products and by-products and evaluation of mass balance were carried out. In these tests, it is confirmed that uranium ingots can be obtained with heating the products more than melting temperature of metal uranium under atmospheric pressure because adhered salt cover the uranium not to oxidize it during uranium cohering. Covered salt can be removed after ingot formation. Inside the ingot, there were a lump of uranium and dark brown colored dross was observed. Material balance of uranium is 77 ∼ 96%, that of plutonium is 71 ∼ 109%, and that of americium that is a volatile substance more than uranium and plutonium become 79 ∼ 119%. Volatilization of americium is very small under the condition of high temperature. (authors)

Uptake of uranium from underground drinking water by chlorella (Chlorella pyrendoidosa)

International Nuclear Information System (INIS)

Singhal, R.K.; Joshi, Shobha; Gurg, R.P.; Shenoy, N.S.; Ferandes, Neychelle; Gopale, Rajesh S.; Jhaveri, A.S.

2002-01-01

Naturally occurring uranium has found at elevated levels i.e. 300-1200 ppb in underground water, especially in the areas located around uranium mines and granite rocks sites. The U.S. Environmental Protection Agency (EPA) recently adopted drinking water standards requiring a maximum uranium concentration of 20 μgl. This limit is based on nephro-toxicity, rather than on radiological hazards. The concentration of uranium is to be monitored along with other parameters in well and other sources of drinking water in these areas. During this work a low cost kit was developed for removing uranium from under-ground water used for drinking purposes. This unit is capable of reducing uranium from 1000 ppb to 15-20 ppb. Chlorella (Chlorella pyrendoidosa), a fresh water algae, was immobilised in sodium alginate in the form of beads by using 0.2 M calcium chloride. These beads were put in container and the water is stirred occasionally. 99-100 % uranium adsorbed was recovered from the beads by using 0.1 M HNO 3 . These results suggest that the uptake of uranium by Chlorella depended upon the physico-chemical adsorption on the cell surface, but not upon the biological activity and that uranium in the algal cells was coupled with the ligands, which can be easily substituted with NO 3 -1 . (author)

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

International Nuclear Information System (INIS)

Koyama, Tadafumi; Yamawaki, Michio

1989-01-01

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

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.

Temperature effect on uranium retention onto Zr{sub 2}O(PO{sub 4}){sub 2} surface; Effet de la temperature sur les mecanismes d'interaction entre l'ion uranyle et l'oxophosphate de zirconium

Energy Technology Data Exchange (ETDEWEB)

Almazan Torres, M.G

2007-03-15

Uranium sorption onto Zr{sub 2}O(PO{sub 4}){sub 2} has been studied between 298 K and 363 K, in 0.1 M NaClO{sub 4} medium. Potentiometric titrations were realized to determine temperature dependency of the acid-base properties (pH(pcn), acidity constants). Classical batch experiments were performed at different temperatures. The sorption experiments revealed that the uranium sorption onto Zr{sub 2}O(PO{sub 4}){sub 2} is favoured with the temperature. Structural characterization of the surface complexes was performed by both Time-Resolved Laser-Induced Fluorescence (TRLIF) and EXAFS spectroscopy. The TRLIF measurements vs. temperature revealed two uranyl surface complexes. No influence of the temperature onto the nature surface complex was observed. The EXAFS analysis showed a splitting of the equatorial oxygen atoms in two shells, corresponding to uranyl bidentate, inner-sphere complexes. The obtained structural uranyl surface complex information was used to simulate (using a constant capacitance model) the sorption edges. The proposed complexes equilibrium model consists of the following surface complexes: (ZrOH){sub 2}UO{sub 2}{sup 2+} and (PO){sub 2}UO{sub 2}. Besides the stability constants for the surface complexes, the thermodynamic parameters {delta}H{sup 0} and {delta}S{sup 0} were determined using the van't Hoff equation. The enthalpy values associated to the U(VI) retention onto Zr{sub 2}O(PO{sub 4}){sub 2}, determined by the temperature dependence of the stability constants, testify that the formation of the complex (PO){sub 2}UO{sub 2} (55 kJ/mol) is endothermic, while no influence of the temperature was observed for the formation of the complex (ZrOH){sub 2}UO{sub 2}{sup 2+}. The adsorption reaction of the last complex is then driven by entropy. In addition, calorimetric measurements of uranium sorption onto Zr{sub 2}O(PO{sub 4}){sub 2} were carried out to directly quantify the enthalpy associated to the retention processes. (author)

Recurrence quantification analysis of extremes of maximum and minimum temperature patterns for different climate scenarios in the Mesochora catchment in Central-Western Greece

Science.gov (United States)

Panagoulia, Dionysia; Vlahogianni, Eleni I.

2018-06-01

A methodological framework based on nonlinear recurrence analysis is proposed to examine the historical data evolution of extremes of maximum and minimum daily mean areal temperature patterns over time under different climate scenarios. The methodology is based on both historical data and atmospheric General Circulation Model (GCM) produced climate scenarios for the periods 1961-2000 and 2061-2100 which correspond to 1 × CO2 and 2 × CO2 scenarios. Historical data were derived from the actual daily observations coupled with atmospheric circulation patterns (CPs). The dynamics of the temperature was reconstructed in the phase-space from the time series of temperatures. The statistically comparing different temperature patterns were based on some discriminating statistics obtained by the Recurrence Quantification Analysis (RQA). Moreover, the bootstrap method of Schinkel et al. (2009) was adopted to calculate the confidence bounds of RQA parameters based on a structural preserving resampling. The overall methodology was implemented to the mountainous Mesochora catchment in Central-Western Greece. The results reveal substantial similarities between the historical maximum and minimum daily mean areal temperature statistical patterns and their confidence bounds, as well as the maximum and minimum temperature patterns in evolution under the 2 × CO2 scenario. A significant variability and non-stationary behaviour characterizes all climate series analyzed. Fundamental differences are produced from the historical and maximum 1 × CO2 scenarios, the maximum 1 × CO2 and minimum 1 × CO2 scenarios, as well as the confidence bounds for the two CO2 scenarios. The 2 × CO2 scenario reflects the strongest shifts in intensity, duration and frequency in temperature patterns. Such transitions can help the scientists and policy makers to understand the effects of extreme temperature changes on water resources, economic development, and health of ecosystems and hence to proceed to

Stabilization of mixed carbides of uranium-plutonium by zirconium. Part 1.: uranium carbide with small additions of zirconium; Etude de la stabilisation des carbures mixtes d'uranium et de plutonium par addition de zirconium. 1. partie: etude des carbures d'uranium avec de faibles additions de zirconium

Energy Technology Data Exchange (ETDEWEB)

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

1969-07-01

Cast carbide samples, being of a high density and purity, are preferable for research purposes, to samples produced by powder metallurgy methods. Samples of uranium carbide with small additions of zirconium (1 to 5 per cent) were cast, as rods, in an arc furnace. A single phase carbide with interesting qualities was produced. As cast, a dendrite structure is observed, which does not disappear, after a treatment at 1900 deg. C during 110 hours. In comparison with uranium monocarbide the compatibility with stainless steel is much improved. The specific heat (between room temperature and 2500 deg. C) is similar to the specific heat of uranium monocarbide. A study of these mixed carbides, but having a part of the uranium replaced by plutonium is under way. (author) [French] Les echantillons de monocarbures obtenus par coulee sont tres interessants pour les recherches experimentales a cause de leur grande purete, de leur densite tres elevee et de la facilite d'obtention des lingots de forme et dimensions variees. On a prepare et coule dans un four a arc des echantillons de carbures d'uranium avec de faibles additions de zirconium (1 a 5 at. pour cent). On obtient ainsi des carbures monophases presentant de meilleures proprietes que le monocarbure d'uranium. A l'etat brut de coulee on observe une structure dendritique qui n'est pas detruite par un traitement thermique de 110 heures a 1900 deg. C. La compatibilite avec l'acier inoxydable 316 (a 925 deg. C pendant 500 heures) est nettement amelioree par rapport a UC. La chaleur specifique (entre la temperature ordinaire et 2500 deg. C) et la densite sont tres peu differentes de celles du monocarbure d'uranium. Une etude concernant les composes U-Pu-Zr-C est actuellement en cours. (auteur)

A study on the oxidation behavior of uranium

International Nuclear Information System (INIS)

Kim, Tae Kook; Kang, Kweon Ho; Kim, Kil Jeang; Kang, Il Sik; Jung, Kyung Whan

1998-03-01

When storing depleted uranium wastes, careful handling is required due to their very high oxidation rates. To determine the oxidation mechanism and oxidation rate of depleted uranium wastes, the most important factors to be considered in their treatment, an experiment was carried out by varying the heating rates of the Air-Controlled Oxidizer. The experiment, showed that depleted uranium wastes are pulverized after complete oxidation because of the density difference and then converted to UO 2 , U 3 O 7 , U 3 O 8 . The grain size of pulverized powder decrease with increased temperature. (author). 30 refs., 5 tabs., 28 figs

Metallization of uranium oxide powders by lithium reduction

International Nuclear Information System (INIS)

Kim, I. S.; Seo, J. S.; Oh, S. C.; Hong, S. S.; Lee, W. K.

2002-01-01

Laboratory scale experiments on the reduction of uranium oxide powders into metal by lithium were performed in order to determine the equipment setup and optimum operation conditions. The method of filtration using the porous magnesia filter was introduced to recover uranium metal powders produced. Based on the laboratory scale experimental results, mock-up scale (20 kg U/batch) metallizer was designed and made. The applicability to the metallization process was estimated with respect to the thermal stability of the porous magnesia filter in the high temperature molten salt, the filtration of the fine uranium metal powders, and the operability of the equipment

Elevated Uranium in Aquifers of the Jacobsville Sandstone

Science.gov (United States)

Sherman, H.; Gierke, J.

2003-12-01

The EPA has announced a new standard for uranium in drinking water of 30 parts per billion (ppb). This maximum contaminant level (MCL) takes effect for community water supplies December 2003. The EPA's ruling has heightened awareness among residential well owners that uranium in drinking water may increase the risk of kidney disease and cancer and has created a need for a quantified, scientific understanding of the occurrence and distribution of uranium isotopes in aquifers. The authors are investigating the occurrence of elevated uranium in northern Michigan aquifers of the Middle Proterozoic Jacobsville sandstone, a red to mottled sequence of sandstones, conglomerates, siltstones and shales deposited as basin fill in the 1.1 Ga Midcontinent rift. Approximately 25% of 300 well water samples tested for isotopic uranium have concentrations above the MCL. Elevated uranium occurrences are distributed throughout the Jacobsville sandstone aquifers stretching across Michigan's Upper Peninsula. However, there is significant variation in well water uranium concentrations (from 0.01 to 190 ppb) and neighboring wells do not necessarily have similar concentrations. The authors are investigating hydrogeologic controls on ground water uranium concentrations in the Jacobsville sandstone, e.g. variations in lithology, mineralogy, groundwater residence time and geochemistry. Approximately 2000' of Jacobsville core from the Amoco St. Amour well was examined in conjunction with the spectral gamma ray log run in the borehole. Spikes in equivalent uranium (eU) concentration from the log are frequently associated with clay and heavy mineral layers in the sandstone core. The lithology and mineralogy of these layers will be determined by analysis of thin sections and x-ray diffraction. A portable spectrometer, model GRS-2000/BL, will be used on the sandstone cliffs along Lake Superior to characterize depositional and lithologic facies of the Jacobsville sandstone in terms of

Yalina booster subcritical assembly performance with low enriched uranium fuel

International Nuclear Information System (INIS)

Talamo, Alberto; Gohar, Yousry

2011-01-01

The YALINA Booster facility is a subcritical assembly located in Minsk, Belarus. The facility has special features that result in fast and thermal neutron spectra in different zones. The fast zone of the assembly uses a lead matrix and uranium fuels with different enrichments: 90% and 36%, 36%, or 21%. The thermal zone of the assembly contains 10% enriched uranium fuel in a polyethylene matrix. This study discusses the performance of the three YALINA Booster configurations with the different fuel enrichments. In order to maintain the same subcriticality level in the three configurations, the number of fuel rods in the thermal zone is increased as the uranium fuel enrichment in the fast zone is decreased. The maximum number of fuel rods that can be loaded in the thermal zone is about 1185. Consequently, the neutron multiplication of the configuration with 21% enriched uranium fuel in the fast zone is enhanced by changing the position of the boron carbide and the natural uranium absorber rods, located between the fast and the thermal zones, to form an annular rather than a square arrangement. (author)

Yalina booster subcritical assembly performance with low enriched uranium fuel

Energy Technology Data Exchange (ETDEWEB)

Talamo, Alberto; Gohar, Yousry, E-mail: alby@anl.gov [Argonne National Laboratory, Lemont, IL (United States)

2011-07-01

The YALINA Booster facility is a subcritical assembly located in Minsk, Belarus. The facility has special features that result in fast and thermal neutron spectra in different zones. The fast zone of the assembly uses a lead matrix and uranium fuels with different enrichments: 90% and 36%, 36%, or 21%. The thermal zone of the assembly contains 10% enriched uranium fuel in a polyethylene matrix. This study discusses the performance of the three YALINA Booster configurations with the different fuel enrichments. In order to maintain the same subcriticality level in the three configurations, the number of fuel rods in the thermal zone is increased as the uranium fuel enrichment in the fast zone is decreased. The maximum number of fuel rods that can be loaded in the thermal zone is about 1185. Consequently, the neutron multiplication of the configuration with 21% enriched uranium fuel in the fast zone is enhanced by changing the position of the boron carbide and the natural uranium absorber rods, located between the fast and the thermal zones, to form an annular rather than a square arrangement. (author)

Uranium mining and rehabilitation: International aspects and examples from Germany

International Nuclear Information System (INIS)

Barthel, F.H.; Mager, D.

1997-01-01

In the period from 1945 to 1994 about 1.87 million t U have been produced worldwide. The maximum of production reached about 70,000 t U in 1981, now the production has fell to about 32,000 t U. Due to the decrease of the annual output, employment in uranium production has decreased, however the productivity has been increased in most countries. As any mining, uranium mining has an impact on the environment. Especially the radioactivity of the ores and waste material may create radiological hazards to the population when protection measures are not observed carefully. The impact of uranium production to the environmental is illustrated by various examples. The costs which are necessary to decommission and rehabilitate uranium production facilities can reach high levels depending on the specifics of the recultivation activities. International examples are given. The production of uranium in Eastern Germany is described briefly, and the reclamation activities of the former Wismut mining and milling facilities is illustrated by selected examples. (author). 5 tabs