Assessment of uranium dioxide fuel performance with the addition of beryllium oxide

Energy Technology Data Exchange (ETDEWEB)

Muniz, Rafael O.R.; Abe, Alfredo; Gomes, Daniel S.; Silva, Antonio T., E-mail: romuniz@usp.br, E-mail: ayabe@ipen.br, E-mail: danieldesouza@gmail.com, E-mail: teixeira@ipen.br [Instituto de Pesquisas Energética s e Nucleares (IPEN/CNEN-SP), São Paulo, SP (Brazil); Giovedi, Claudia, E-mail: claudia.giovedi@labrisco.usp.br [Universidade de Sao Paulo (LabRisco/USP), Sao Paulo, SP (Brazil). Lab. de Análise, Avaliação e Gerenciamento de Risco; Aguiar, Amanda A., E-mail: amanda.abati.aguiar@gmail.com [Centro Tecnológico da Marinha em São Paulo (CTMSP), São Paulo, SP (Brazil)

2017-07-01

The Fukushima Daiichi accident in 2011 pointed the problem related to the hydrogen generation under accident scenarios due to the oxidation of zirconium-based alloys widely used as fuel rod cladding in water-cooled reactors. This problem promoted research programs aiming the development of accident tolerant fuels (ATF) which are fuels that under accident conditions could keep longer its integrity enabling the mitigation of the accident effects. In the framework of the ATF program, different materials have been studied to be applied as cladding to replace zirconium-based alloy; also efforts have been made to improve the uranium dioxide thermal conductivity doping the fuel pellet. This paper evaluates the addition of beryllium oxide (BeO) to the uranium dioxide in order to enhance the thermal conductivity of the fuel pellet. Investigations performed in this area considering the addition of 10% in volume of BeO, resulting in the UO{sub 2}-BeO fuel, have shown good results with the improvement of the fuel thermal conductivity and the consequent reduction of the fuel temperatures under irradiation. In this paper, two models obtained from open literature for the thermal conductivity of UO{sub 2}- BeO fuel were implemented in the FRAPCON 3.5 code and the results obtained using the modified code versions were compared. The simulations were carried out using a case available in the code documentation related to a typical pressurized water reactor (PWR) fuel rod irradiated under steady state condition. The results show that the fuel centerline temperatures decrease with the addition of BeO, when compared to the conventional UO{sub 2} pellet, independent of the model applied. (author)

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

Design of a Uranium Dioxide Spheroidization System

Science.gov (United States)

Cavender, Daniel P.; Mireles, Omar R.; Frendi, Abdelkader

2013-01-01

The plasma spheroidization system (PSS) is the first process in the development of tungsten-uranium dioxide (W-UO2) fuel cermets. The PSS process improves particle spherocity and surface morphology for coating by chemical vapor deposition (CVD) process. Angular fully dense particles melt in an argon-hydrogen plasma jet at between 32-36 kW, and become spherical due to surface tension. Surrogate CeO2 powder was used in place of UO2 for system and process parameter development. Particles range in size from 100 - 50 microns in diameter. Student s t-test and hypothesis testing of two proportions statistical methods were applied to characterize and compare the spherocity of pre and post process powders. Particle spherocity was determined by irregularity parameter. Processed powders show great than 800% increase in the number of spherical particles over the stock powder with the mean spherocity only mildly improved. It is recommended that powders be processed two-three times in order to reach the desired spherocity, and that process parameters be optimized for a more narrow particles size range. Keywords: spherocity, spheroidization, plasma, uranium-dioxide, cermet, nuclear, propulsion

Method and device for the dry preparation of ceramic uranium dioxide nuclear fuel wastes

International Nuclear Information System (INIS)

Pirk, H.; Roepenack, H.; Goeldner, U.

1977-01-01

Reprocessing of waste, resulting from the production of ceramic sintered bodies from uranium dioxide for use as nuclear fuel, in a dry process into very finely dispersed pure U 3 O 8 powder may be improved by applying vibrating screening during oxidation. An appropriate device is described. (UWI) [de

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

Energy Technology Data Exchange (ETDEWEB)

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

2017-04-01

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

Development of Nitride Coating Using Atomic Layer Deposition for Low-Enriched Uranium Fuel Powder

Science.gov (United States)

Bhattacharya, Sumit

High-performance research reactors require fuel that operates at high specific power and can withstand high fission density, but at relatively low temperatures. The design of the research reactor fuels is done for efficient heat emission, and consists of assemblies of thin-plates cladding made from aluminum alloy. The low-enriched fuels (LEU) were developed for replacing high-enriched fuels (HEU) for these reactors necessitates a significantly increased uranium density in the fuel to counterbalance the decrease in enrichment. One of the most promising new fuel candidate is U-Mo alloy, in a U-Mo/Al dispersion fuel form, due to its high uranium loading as well as excellent irradiation resistance performance, is being developed extensively to convert from HEU fuel to LEU fuel for high-performance research reactors. However, the formation of an interaction layer (IL) between U-Mo particles and the Al matrix, and the associated pore formation, under high heat flux and high burnup conditions, degrade the irradiation performance of the U-Mo/Al dispersion fuel. From the recent tests results accumulated from the surface engineering of low enriched uranium fuel (SELENIUM) and MIR reactor displayed that a surface barrier coating like physical vapor deposited (PVD) zirconium nitride (ZrN) can significantly reduce the interaction layer. The barrier coating performed well at low burn up but above a fluence rate of 5x 1021 ions/cm2 the swelling reappeared due to formation interaction layer. With this result in mind the objective of this research was to develop an ultrathin ZrN coating over particulate uranium-molybdenum nuclear fuel using a modified savannah 200 atomic layer deposition (ALD) system. This is done in support of the US Department of Energy's (DOE) effort to slow down the interaction at fluence rate and reach higher burn up for high power research reactor. The low-pressure Savannah 200 ALD system is modified to be designed as a batch powder coating system using the

Pyrolytic carbon coatings for nuclear fuels from commercial butane

International Nuclear Information System (INIS)

Abdelrazek, I.D.; Abdelhalim, A.S.

1976-01-01

Uranium dioxide and graphite semi-spherical particles (average diameter = 300 um) were coated with pyrolytic carbon at relatively low temperatures (800 to 1200 0 C). The spouting gas was a mixture of commercial butane and nitrogen. The hydrocarbon served as a source for carbon whereas nitrogenated as a diluent and a support for the bed. The total gas flow rate was 3.5 lit/min and the hydrocarbon content varied from 3 to 10%. Coating efficiencies ranging from 4 to 25 percent were obtained. The densities of the coatings varied from 1.25 g/cm 3 (which corresponds to coatings of laminar microstructures) and 1.82 g/cm 3 (which suggests the formation of isotropic coatings. Metallographic examination (using polarized light) of the pyrolytic carbon formed at the experimental conditions indicated the possibility of using the coatings for nuclear fuel applications

Gas phase deposition of oxide and metal-oxide coatings on fuel particles

International Nuclear Information System (INIS)

Patokin, A.P.; Khrebtov, V.L.; Shirokov, B.M.

2008-01-01

Production processes and properties of oxide (Al 2 O 3 , ZrO 2 ) and metal-oxide (Mo-Al 2 O 3 , Mo-ZrO 2 , W-Al 2 O 3 , W-ZrO 2 ) coatings on molybdenum substrates and uranium dioxide fuel particles were investigated. It is shown that the main factors that have an effect on the deposition rate, density, microstructure and other properties of coatings are the deposition temperature, the ratio of H 2 and CO 2 flow rates, the total reactor pressure and the ratio of partial pressures of corresponding metal chlorides during formation of metal-oxide coatings

Method for preparing a sinterable uranium dioxide powder

International Nuclear Information System (INIS)

Thornton, T.A.; Holaday, V.D. Jr.

1985-01-01

This invention provides an improved method for preparing a sinterable uranium dioxide powder for the preparation of nuclear fuel, using microwave radiation in a microwave induction furnace. The starting compound may be uranyl nitrate hexahydrate, ammonium diuranate or ammonium uranyl carbonate. The starting compound is heated in a microwave induction furnace for a period of time sufficient for compound decomposition. The decomposed compound is heated in a microwave induction furnace in a reducing atmosphere for a period of time sufficient to reduce the decomposed compound to uranium dioxide powder

Electronic structure of the actinides and their dioxides. Application to the defect formation energy and krypton solubility in uranium dioxide

International Nuclear Information System (INIS)

Petit, T.; CEA Centre d'Etudes de Grenoble, 38

1996-01-01

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

Critical experiments simulating accidental water immersion of highly enriched uranium dioxide fuel elements

International Nuclear Information System (INIS)

Ponomarev-Stepnoi, N.N.; Glushkov, L.S.

2003-01-01

The paper focuses on experimental analysis of nuclear criticality safety at accidental water immersion of fuel elements of the Russian TOPAZ-2 space nuclear power system reactor. The structure of water-moderated heterogeneous critical assemblies at the NARCISS facility is described in detail, including sizes, compositions, densities of materials of the main assembly components for various core configurations. Critical parameters of the assemblies measured for varying number of fuel elements, height of fuel material in fuel elements and their arrangement in the water moderator with a uniform or variable spacing are presented. It has been found from the experiments that at accidental water immersion of fuel elements involved, the minimum critical mass equal to approximately 20 kg of uranium dioxide is achieved at 31-37 fuel elements. The paper gives an example of a physical model of the water-moderated heterogeneous critical assembly with a detailed characterization of its main components that can be used for calculations using different neutronic codes, including Monte Carlo ones. (author)

Study on microstructure change of Uranium nitride coated U-7wt%Mo powder by heat treatment

Energy Technology Data Exchange (ETDEWEB)

Cho, Woo Hyoung; Park, Jae Soon; Lee, Hae In; Kim, Woo Jeong; Yang, Jae Ho; Park, Jong Man [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2011-10-15

Uranium-molybdenum alloy particle dispersion fuel in an aluminum matrix with a high uranium density has been developed for a high performance research reactor in the RERTR program. In order to retard the fuel-matrix interaction in U-Mo/Al dispersion fuel in which the U-Mo fuel particles were dispersed in Al matrix, nitride layer coated U-Mo fuel particle has been designed and techniques to fabricate nitride-layer coated U-7wt%Mo particles have been developed in our lab. In this study, uranium nitride coated U-Mo particle has heat treatment for several times and degree. And we suggested for interaction layer remedy in U-Mo dispersion fuel. We investigate effect of heat treatment interaction layer evolution on uranium nitride coated U-Mo powder. The EDS and XRD analysis to investigate the phase evolution in uranium nitride coated layer is also a part of the present work

Determination of the stoichiometric ratio uranium dioxide samples

International Nuclear Information System (INIS)

Moura, Sergio Carvalho

1999-01-01

The determination of the O/U stoichiometric ratio in uranium dioxide is an important parameter in order to qualify nuclear fuels. The excess oxygen in the crystallographic structure can cause changes in the physico-chemical properties of this compound such as variation of the thermal conductivity alterations, fuel plasticity and others, affecting the efficiency of this material when it is utilized as nuclear fuel in the reactor core. The purpose of this work is to evaluate methods for the determination of uranium oxide samples from two different production processes, using gravimetric, voltammetric and X-ray diffraction techniques. After the evaluation of these techniques, the main aspect of this work is to define a reliable methodology in order to characterize the behavior of uranium oxide. The methodology used in this work consisted of two different steps: utilization of gravimetric and volumetric methods in order to determine the ratio in uranium dioxide samples; utilization of X-ray diffraction technique in order to determine the lattice parameters using patterns and application of the Rietveld method during refining of the structural data. As a result of the experimental part of this work it was found that the X-ray diffraction analysis performs better and detects the presence of more phases than gravimetric and voltammetric techniques, not sensitive enough in this detection. (author)

Uranium dioxide pellets

International Nuclear Information System (INIS)

Zawidzki, T.W.

1979-01-01

Sintered uranium dioxide pellets composed of particles of size > 50 microns suitable for power reactor use are made by incorporating a small amount of sulphur into the uranium dioxide before sintering. The increase in grain size achieved results in an improvement in overall efficiency when such pellets are used in a power reactor. (author)

Study of non stoichiometric uranium dioxide samples (UO2)

International Nuclear Information System (INIS)

Moura, Sergio C.; Lima, Nelson B. de; Bustillos, Jose O.V.

1999-01-01

The gravimetric and voltammetric methods for determination of non-stoichiometric O/U ratio in uranium dioxide used as nuclear fuel are discussed in this work. The oxidation of uranium oxide is very complex due to many phase changes. gravimetric and voltammetric methods do not detect phase changes. The results of this work shown that, to evaluate both methods is requiring to be done Rietveld methods by x-ray diffraction data to identify the uranium oxide phase changes. (author)

Hardened over-coating fuel particle and manufacture of nuclear fuel using its fuel particle

International Nuclear Information System (INIS)

Yoshimuda, Hideharu.

1990-01-01

Coated-fuel particles comprise a coating layer formed by coating ceramics such as silicon carbide or zirconium carbide and carbons, etc. to a fuel core made of nuclear fuel materials. The fuel core generally includes oxide particles such as uranium, thorium and plutonium, having 400 to 600 μm of average grain size. The average grain size of the coated-fuel particle is usually from 800 to 900 μm. The thickness of the coating layer is usually from 150 to 250 μm. Matrix material comprising a powdery graphite and a thermosetting resin such as phenol resin, etc. is overcoated to the surface of the coated-fuel particle and hardened under heating to form a hardened overcoating layer to the coated-fuel particle. If such coated-fuel particles are used, cracks, etc. are less caused to the coating layer of the coated-fuel particles upon production, thereby enabling to prevent the damages to the coating layer. (T.M.)

Beryllium Project: developing in CDTN of uranium dioxide fuel pellets with addition of beryllium oxide to increase the thermal conductivity

International Nuclear Information System (INIS)

Ferreira, Ricardo Alberto Neto; Camarano, Denise das Merces; Miranda, Odair; Grossi, Pablo Andrade; Andrade, Antonio Santos; Queiroz, Carolinne Mol; Gonzaga, Mariana de Carvalho Leal

2013-01-01

Although the nuclear fuel currently based on pellets of uranium dioxide be very safe and stable, the biggest problem is that this material is not a good conductor of heat. This results in an elevated temperature gradient between the center and its lateral surface, which leads to a premature degradation of the fuel, which restricts the performance of the reactor, being necessary to change the fuel before its full utilization. An increase of only 5 to 10 percent in its thermal conductivity, would be a significant increase. An increase of 50 percent would be a great improvement. A project entitled 'Beryllium Project' was developed in CDTN - Centro de Desenvolvimento da Tecnologia Nuclear, which aimed to develop fuel pellets made from a mixture of uranium dioxide microspheres and beryllium oxide powder to obtain a better heat conductor phase, filling the voids between the microspheres to increase the thermal conductivity of the pellet. Increases in the thermal conductivity in the range of 8.6% to 125%, depending on the level of addition employed in the range of 1% to 14% by weight of beryllium oxide, were obtained. This type of fuel promises to be safer than current fuels, improving the performance of the reactor, in addition to last longer, resulting in great savings. (author)

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

International Nuclear Information System (INIS)

Hannerz, K.

1976-01-01

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

Present state and problems of uranium fuel fabrication businesses

International Nuclear Information System (INIS)

Yuki, Akio

1981-01-01

The businesses of uranium fuel fabrication converting uranium hexafluoride to uranium dioxide powder and forming fuel assemblies are the field of most advanced industrialization among nuclear fuel cycle industries in Japan. At present, five plants of four companies engage in this business, and their yearly sales exceeded 20 billion yen. All companies are planning the augmentation of installation capacity to meet the growth of nuclear power generation. The companies of uranium fuel fabrication make the nuclear fuel of the specifications specified by reactor manufacturers as the subcontractors. In addition to initially loaded fuel, the fuel for replacement is required, therefore the demand of uranium fuel is relatively stable. As for the safety of enriched uranium flowing through the farbicating processes, the prevention of inhaling uranium powder by workers and the precaution against criticality are necessary. Also the safeguard measures are imposed so as not to convert enriched uranium to other purposes than peacefull ones. The strict quality control and many times of inspections are carried out to insure the soundness of nuclear fuel. The growth of the business of uranium fuel fabrication and the regulation of the businesses by laws are described. As the problems for the future, the reduction of fabrication cost, the promotion of research and development and others are pointed out. (Kako, I.)

A METHOD OF PREPARING URANIUM DIOXIDE

Science.gov (United States)

Scott, F.A.; Mudge, L.K.

1963-12-17

A process of purifying raw, in particular plutonium- and fission- products-containing, uranium dioxide is described. The uranium dioxide is dissolved in a molten chloride mixture containing potassium chloride plus sodium, lithium, magnesium, or lead chloride under anhydrous conditions; an electric current and a chlorinating gas are passed through the mixture whereby pure uranium dioxide is deposited on and at the same time partially redissolved from the cathode. (AEC)

The cohesive energy of uranium dioxide and thorium dioxide

International Nuclear Information System (INIS)

Childs, B.G.

1958-08-01

Theoretical values have been calculated of the heats of formation of uranium dioxide and thorium dioxide on the assumption that the atomic binding forces in these solids are predominantly ionic in character. The good agreement found between the theoretical and observed values shows that the ionic model may, with care, be used in calculating the energies of defects in the uranium and thorium dioxide crystal structures. (author)

A new mechanistic and engineering fission gas release model for a uranium dioxide fuel

International Nuclear Information System (INIS)

Lee, Chan Bock; Yang, Yong Sik; Kim, Dae Ho; Kim, Sun Ki; Bang, Je Geun

2008-01-01

A mechanistic and engineering fission gas release model (MEGA) for uranium dioxide (UO 2 ) fuel was developed. It was based upon the diffusional release of fission gases from inside the grain to the grain boundary and the release of fission gases from the grain boundary to the external surface by the interconnection of the fission gas bubbles in the grain boundary. The capability of the MEGA model was validated by a comparison with the fission gas release data base and the sensitivity analyses of the parameters. It was found that the MEGA model correctly predicts the fission gas release in the broad range of fuel burnups up to 98 MWd/kgU. Especially, the enhancement of fission gas release in a high-burnup fuel, and the reduction of fission gas release at a high burnup by increasing the UO 2 grain size were found to be correctly predicted by the MEGA model without using any artificial factor. (author)

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

A density functional theory study of uranium-doped thoria and uranium adatoms on the major surfaces of thorium dioxide

Energy Technology Data Exchange (ETDEWEB)

Shields, Ashley E. [Department of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ (United Kingdom); Santos-Carballal, David [School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff CF10 3AT (United Kingdom); Leeuw, Nora H. de, E-mail: DeLeeuwN@Cardiff.ac.uk [Department of Chemistry, University College London, 20 Gordon Street, London WC1H 0AJ (United Kingdom); School of Chemistry, Cardiff University, Main Building, Park Place, Cardiff CF10 3AT (United Kingdom)

2016-05-15

Thorium dioxide is of significant research interest for its use as a nuclear fuel, particularly as part of mixed oxide fuels. We present the results of a density functional theory (DFT) study of uranium-substituted thorium dioxide, where we found that increasing levels of uranium substitution increases the covalent nature of the bonding in the bulk ThO{sub 2} crystal. Three low Miller index surfaces have been simulated and we propose the Wulff morphology for a ThO{sub 2} particle and STM images for the (100), (110), and (111) surfaces studied in this work. We have also calculated the adsorption of a uranium atom and the U adatom is found to absorb strongly on all three surfaces, with particular preference for the less stable (100) and (110) surfaces, thus providing a route to the incorporation of uranium into a growing thoria particle. - Highlights: • Uranium substitution in ThO{sub 2} is found to increase the covalent nature of the ionic bonding. • The (111), (110), and (100) surfaces of ThO{sub 2} are studied and the particle morphology is proposed. • STM images of the (111), (110), and (100) surfaces of ThO{sub 2} are simulated. • Uranium adsorption on the major surfaces of ThO{sub 2} is studied.

Pyrochemical reduction of uranium dioxide and plutonium dioxide by lithium metal

International Nuclear Information System (INIS)

Usami, T.; Kurata, M.; Inoue, T.; Sims, H.E.; Beetham, S.A.; Jenkins, J.A.

2002-01-01

The lithium reduction process has been developed to apply a pyrochemical recycle process for oxide fuels. This process uses lithium metal as a reductant to convert oxides of actinide elements to metal. Lithium oxide generated in the reduction would be dissolved in a molten lithium chloride bath to enhance reduction. In this work, the solubility of Li 2 O in LiCl was measured to be 8.8 wt% at 650 deg. C. Uranium dioxide was reduced by Li with no intermediate products and formed porous metal. Plutonium dioxide including 3% of americium dioxide was also reduced and formed molten metal. Reduction of PuO 2 to metal also occurred even when the concentration of lithium oxide was just under saturation. This result indicates that the reduction proceeds more easily than the prediction based on the Gibbs free energy of formation. Americium dioxide was also reduced at 1.8 wt% lithium oxide, but was hardly reduced at 8.8 wt%

Assessment of current atomic scale modelling methods for the investigation of nuclear fuels under irradiation: Example of uranium dioxide

International Nuclear Information System (INIS)

Bertolus, M.; Freyss, M.; Krack, M.; Devanathan, R.

2015-01-01

We focus here on the assessment of the description of interatomic interactions in uranium dioxide using, on the one hand, electronic structure methods, in particular in the Density Functional Theory (DFT) framework, and on the other hand, empirical potential methods. These two types of methods are complementary, the former enabling results to be obtained from a minimal amount of input data and further insight into the electronic and magnetic properties to be achieved, while the latter are irreplaceable for studies where a large number of atoms need to be considered. We consider basic properties as well as specific ones, which are important for the description of nuclear fuel under irradiation. These are especially energies, which are the main data passed on to higher scale models. For this exercise, we limit ourselves to uranium dioxide (UO 2 ) because of the extensive amount of studies available on this system. (authors)

Development of an environmentally friendly protective coating for the depleted uranium-0.75 wt% titanium alloy

International Nuclear Information System (INIS)

Roeper, Donald F.; Chidambaram, Devicharan; Clayton, Clive R.; Halada, Gary P.; Derek Demaree, J.

2006-01-01

Molybdenum oxide-based conversion coatings have been formed on the surface of the depleted uranium-0.75 wt% titanium alloy using either concentrated nitric acid or fluorides for surface activation prior to coating formation. The acid-activated surface forms a coating that offers corrosion protection after a period of aging, when uranium species have migrated to the surface. X-ray photoelectron spectroscopy (XPS) revealed that the protective coating is primarily a polymolybdate bound to a uranyl ion. Rutherford backscattering spectroscopy (RBS) on the acid-activated coatings also shows uranium dioxide migrating to the surface. The fluoride-activated surface does not form a protective coating and there are no uranium species on the surface as indicated by XPS. The coating on the fluoride-activated samples has been found to contain a mixture of molybdenum oxides of which the main component is molybdenum trioxide and a minor component of an Mo(V) oxide

Ceramics as nuclear reactor fuels

International Nuclear Information System (INIS)

Reeve, K.D.

1975-01-01

Ceramics are widely accepted as nuclear reactor fuel materials, for both metal clad ceramic and all-ceramic fuel designs. Metal clad UO 2 is used commercially in large tonnages in five different power reactor designs. UO 2 pellets are made by familiar ceramic techniques but in a reactor they undergo complex thermal and chemical changes which must be thoroughly understood. Metal clad uranium-plutonium dioxide is used in present day fast breeder reactors, but may eventually be replaced by uranium-plutonium carbide or nitride. All-ceramic fuels, which are necessary for reactors operating above about 750 0 C, must incorporate one or more fission product retentive ceramic coatings. BeO-coated BeO matrix dispersion fuels and silicate glaze coated UO 2 -SiO 2 have been studied for specialised applications, but the only commercial high temperature fuel is based on graphite in which small fuel particles, each coated with vapour deposited carbon and silicon carbide, are dispersed. Ceramists have much to contribute to many aspects of fuel science and technology. (author)

Contribution to the study of uranium dioxide aqueous corrosion mechanisms

International Nuclear Information System (INIS)

Gallien, J.-P.

1994-01-01

The corrosion of uranium dioxide by a synthetical ground water has been studied in order to understand the behaviour of nuclear fuels in the hypothesis of a direct storage. An original leaching unit has been carried out in order to control the parameters occurring in the oxidation-dissolution of the uranium dioxide and to condition the leachate (in particular the temperature and the partial pressure of the carbon dioxide). A ground water in equilibrium with the geological enveloping site has been reconstituted from data acquired on the site. The influence of two parameters has been followed: the carbon dioxide carbon pressure and the redox potential. Each experiment has been carried out at 96 C during one month and the time-history of the solutions and of the solids has been studied. In oxidizing conditions, the uranium concentration in solution has been controlled by an U(VI) complex (one oxide, one hydroxide or a carbonate). The possibility of a control by an U(IV) complex (as coffinite, uraninite or uraninite B) has been confirmed in the case of reducing leaching. An original interpretation of the Rutherford backscattering spectra has allowed to describe the decomposition of the samples in a succession of layers of different densities. A very good agreement between the analyses of the solids and those of the solutions has been obtained in the experiments occurring in reducing conditions. Complementary leaching involving solutions containing stable isotopes (deuterium, O 18 ) have revealed the formation of an hydrated layer and the contribution of grain boundaries to the corrosion phenomenon of uranium dioxide. The results of the current hydro-geochemistry study on the uranium Oklo deposit prove the realism of the experiments that have been carried out in the laboratory. (O.M.)

Thermal Cycling of Uranium Dioxide - Tungsten Cermet Fuel Specimens

Energy Technology Data Exchange (ETDEWEB)

Gripshover, P.J.; Peterson, J.H.

1969-12-08

In phase I tungsten clad cermet fuel specimens were thermal cycled, to study the effects of fuel loading, fuel particle size, stablized fuel, duplex coatings, and fabrication techniques on dimensional stability during thermal cycling. In phase II the best combination of the factors studies in phase I were combined in one specimen for evaluation.

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

Energy Technology Data Exchange (ETDEWEB)

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

1996-09-28

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

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

International Nuclear Information System (INIS)

1973-01-01

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

Study of the changes of uranium dioxide properties resulting from sintering; Izucavanje procesa sinterovanja urandioksida sa gledista promene karakteristicnih osobina

Energy Technology Data Exchange (ETDEWEB)

Ristic, M M [Institute of Nuclear Sciences Vinca, Laboratorija za reaktorske materijale, Beograd (Serbia and Montenegro)

1962-12-15

Uranium dioxide powder used for studying the sintering process having grain size 63 {mu}. Sintering was performed in the temperature interval from 1000 - 1300 deg C in argon atmosphere. The O/U ratio of the used uranium dioxide was 2.07. Densities obtained by sintering under the mentioned conditions were not higher than 91% TG (theoretical density). This showed that the mentioned conditions were optimal, but the uranium dioxide obtained could be used for studying the radiation damage of fuel.

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

Corrosion resistant coatings for uranium and uranium alloys

International Nuclear Information System (INIS)

Weirick, L.J.; Lynch, C.T.

1977-01-01

Coatings to prevent the corrosion of uranium and uranium alloys are considered in two military applications: kinetic energy penetrators and aircraft counterweights. This study, which evaluated organic films and metallic coatings, demonstrated that the two most promising coatings are based on an electrodeposited nickel system and a galvanized zinc system

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)

Penetrate-leach dissolution of zirconium-clad uranium and uranium dioxide fuels

International Nuclear Information System (INIS)

Harmon, H.D.

1975-01-01

A new decladding-dissolution process was developed for zirconium-clad uranium metal and UO 2 fuels. The proposed penetrate-leach process consists of penetrating the zirconium cladding with Alniflex solution (2M HF--1M HNO 3 --1M Al(NO 3 ) 3 --0.1M K 2 Cr 2 O 7 ) and of leaching the exposed core with 10M HNO 3 . Undissolved cladding pieces are discarded as solid waste. Periodic HF and HNO 3 additions, efficient agitation, and in-line zirconium analyses are required for successful control of ZrF 4 and/or AlF 3 precipitation during the cladding-penetration step. Preliminary solvent extraction studies indicated complete recovery of uranium with 30 vol. percent tributyl phosphate (TBP) from both Alniflex solution and blended Alniflex-HNO 3 leach solutions. With 7.5 vol. percent TBP, high extractant/feed flow ratios and low scrub flows are required for satisfactory uranium recovery from Alniflex solution. Modified waste-handling procedures may be required for Alniflex waste, because it cannot be evaporated before neutralization and large quantities of solids are generated on neutralization. The effect of unstable UZr 3 (epsilon phase of uranium-zirconium system) on the safety of penetrate-leach dissolution was investigated

Surface Characterization and Electrochemical Oxidation of Metal Doped Uranium Dioxide

Energy Technology Data Exchange (ETDEWEB)

Lee, Jeongmook; Kim, Jandee; Youn, Young-Sang; Kim, Jong-Goo; Ha, Yeong-Keong; Kim, Jong-Yun [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2016-10-15

Trivalent element in UO{sub 2} matrix makes the oxygen vacancy from loss of oxygen for charge compensation. Tetravalent element alters lattice parameter of UO{sub 2} due to diameter difference between the tetravalent element and replaced U. These structural changes have significant effect on not only relevant fuel performance but also the kinetics of fuel oxidation. Park and Olander explained the stabilization of Ln (III)-doped UO{sub 2} against oxidation based on oxygen potential calculations. In this work, we have been investigated the effect of Gd{sup 3+} and Th{sup 4+} doping on the UO{sub 2} structure with Raman spectroscopy and X-ray diffraction to characterize the surface structure of nuclear fuel material. For Gd doped UO{sub 2}, its electrochemical oxidation behaviors are also investigated. The Gd and Th doped uranium dioxide solid solution pellets with various doping level were investigated by XRD, Raman spectroscopy, SEM, electrochemical experiments to investigate surface structure and electro chemical oxidation behaviors. The lattice parameter evaluated from XRD spectra indicated the formation of solid solutions. Raman spectra showed the existence of the oxygen vacancy. SEM images showed the grain structure on the surface of Gd doped uranium dioxide depending on doping level and oxygen-to-metal ratio.

Features of spherical uranium-graphite HTGR fuel elements control

International Nuclear Information System (INIS)

Kreindlin, I.I.; Oleynikov, P.P.; Shtan, A.S.

1985-01-01

Control features of spherical HTGR uranium-graphite fuel elements with spherical coated fuel particles are mainly determined by their specific construction and fabrication technology. The technology is chiefly based on methods of ceramic fuel (fuel microspheres fabrication) and graphite production practice it is necessary to deal with a lot of problems from determination of raw materials properties to final fuel elements testing. These procedures are described

Features of spherical uranium-graphite HTGR fuel elements control

Energy Technology Data Exchange (ETDEWEB)

Kreindlin, I I; Oleynikov, P P; Shtan, A S

1985-07-01

Control features of spherical HTGR uranium-graphite fuel elements with spherical coated fuel particles are mainly determined by their specific construction and fabrication technology. The technology is chiefly based on methods of ceramic fuel (fuel microspheres fabrication) and graphite production practice it is necessary to deal with a lot of problems from determination of raw materials properties to final fuel elements testing. These procedures are described.

Results of fuel elements fabrication on the basis of increased concentration dioxide fuel for research reactors

International Nuclear Information System (INIS)

Alexandrov, A.B.; Afanasiev, V.L.; Enin, A.A.; Suprun, V.B.

1996-01-01

According to the Russian Reduced Enrichment for Research and Test Reactors (RERTR) program, that were constructed under the Russian projects, at the Novosibirsk Chemical Concentrates Plant the pilot series of different configuration (WR-M2, MR, IRT-4M) fuel elements, based on increased concentration uranium dioxide fuel, have been fabricated for reactor tests. Comprehensive fabricated fuel elements quality estimation has been carried out. (author)

Development of Coated Particle Fuel Technology

International Nuclear Information System (INIS)

Lee, Young Woo; Kim, B. G.; Kim, S. H.

2007-06-01

Uranium kernel fabrication technology using a wet chemical so-gel method, a key technology in the coated particle fuel area, is established up to the calcination step and the first sintering of UO2 kernel was attempted. Experiments on the parametric study of the coating process using the surrogate ZrO2 kernel give the optimum conditions for the PyC and SiC coating layer and ZrC coating conditions were obtained for the vaporization of the ZrCl4 precursor and coating condition from ZrC coating experiments using plate-type graphite substrate. In addition, by development of fuel performance analysis code a part of the code system is completed which enables the participation to the benchmark calculation and comparison in the IAEA collaborated research program. The technologies for irradiation and post irradiation examination, which are important in developing the HTGR fuel technology of its first kind in Korea was started to develop and, through a feasibility study and preliminary analysis, the technologies required to be developed are identified for further development as well as the QC-related basic technologies are reviewed, analyzed and identified for the own technology development. Development of kernel fabrication technology can be enhanced for the remaining sintering technology and completed based on the technologies developed in this phase. In the coating technology, the optimum conditions obtained using a surrogate ZrO2 kernel material can be applied for the uranium kernel coating process development. Also, after completion of the code development in the next phase, more extended participation to the international collaboration for benchmark calculation can be anticipated which will enable an improvement of the whole code system. Technology development started in this phase will be more extended and further focused on the detailed technology development to be required for the related technology establishment

Nuclear fuel elements

International Nuclear Information System (INIS)

Obara, Hiroshi.

1981-01-01

Purpose: To suppress iodine release thereby prevent stress corrosion cracks in fuel cans by dispersing ferrous oxide at the outer periphery of sintered uranium dioxide pellets filled and sealed within zirconium alloy fuel cans of fuel elements. Constitution: Sintered uranium dioxide pellets to be filled and sealed within a zirconium alloy fuel can are prepared either by mixing ferric oxide powder in uranium dioxide powder, sintering and then reducing at low temperature or by mixing iron powder in uranium dioxide powder, sintering and then oxidizing at low temperature. In this way, ferrous oxide is dispersed on the outer periphery of the sintered uranium dioxide pellets to convert corrosive fission products iodine into iron iodide, whereby the iodine release is suppressed and the stress corrosion cracks can be prevented in the fuel can. (Moriyama, K.)

Long-term testing of HTR fuel elements in the Federal Republic of Germany

International Nuclear Information System (INIS)

Nickel, H.

1986-12-01

The extensive results from irradiation experiments carried out on coated particles, on graphitic matrices of different composition and on integral fuel elements have shown that the spherical fuel elements with high-enriched uranium/thorium mixed-oxide particles and optimized graphitic matrix are available for use in the planned HTR facilities. A concentrated qualification programme is on the way in order to bring the fuel elements with particles from low-enriched uranium dioxide (LEU) and TRISO coating to a comparable level of experience and knowledge, i.e. to make them licensable for the planned HTR facilities. (orig.) [de

Micromechanical approach of behavior of uranium dioxide nuclear fuel

International Nuclear Information System (INIS)

Soulacroix, Julian

2014-01-01

Uranium dioxide (UO 2 ) is the reference fuel for pressurized water nuclear reactors. Our study deals with understanding and modeling of mechanical behavior at the microstructure scale at low temperatures (brittle fracture) and high temperature (viscoplastic strain). We have first studied the geometrical properties of polycrystals at large and of UO 2 polycrystal more specifically. As of now, knowledge of this behavior in the brittle fracture range is limited. Consequently, we developed an experimental method which allows better understanding of brittle fracture phenomenon at grain scale. We show that fracture is fully intra-granular and {100} planes seem to be the most preferential cleavage planes. Experimental results are directly used to deduce constitutive equations of intra-granular brittle fracture at crystal scale. This behavior is then used in 3D polycrystal simulation of brittle fracture. The full field calculation gives access to the initiation of fracture and propagation of the crack through the grains. Finally, we developed a mechanical behavior model of UO 2 in the viscoplastic range. We first present constitutive equations at macroscopic scale which accounts for an ageing process caused by migration of defects towards dislocations. Secondly, we have developed a crystal plasticity model which was fitted to UO 2 . This model includes the rotation of the crystal lattice. We present examples of polycrystalline simulations. (author) [fr

Sintered nuclear fuel and method of preparing same

International Nuclear Information System (INIS)

Abate-Daga, G.; Amato, I.

1975-01-01

A description is given of a method of preparing a nuclear fuel containing a consumable nuclear poison uniformly distributed therein in the form of coated micro-spheres of between 10 and 2,000 microns diameter, consisting in preparing sintered micro-spheres of the consumable poison, covering those micro-spheres with a protective coating and incorporating the coated micro-spheres into uranium dioxide powder, followed by sintering

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

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

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)

Fracture of Zircaloy cladding by interactions with uranium dioxide pellets in LWR fuel rods. Technical report 10

International Nuclear Information System (INIS)

Smith, E.; Ranjan, G.V.; Cipolla, R.C.

1976-11-01

Power reactor fuel rod failures can be caused by uranium dioxide fuel pellet-Zircaloy cladding interactions. The report summarizes the current position attained in a detailed theoretical study of Zircaloy cladding fracture caused by the growth of stress corrosion cracks which form near fuel pellet cracks as a consequence of a power increase after a sufficiently high burn-up. It is shown that stress corrosion crack growth in irradiated Zircaloy must be able to proceed at very low stress intensifications if uniform friction effects are operative at the fuel-cladding interface, when the interfacial friction coefficient is less than unity, when a symmetric distribution of fuel cracks exists, and when symmetric interfacial slippage occurs (i.e., ''uniform'' conditions). Otherwise, the observed fuel rod failures must be due to departures from ''uniform'' conditions, and a very high interfacial friction coefficient and particularly fuel-cladding bonding, are means of providing sufficient stess intensification at a cladding crack tip to explain the occurrence of cladding fractures. The results of the investigation focus attention on the necessity for reliable experimental data on the stress corrosion crack growth behavior of irradiated Zircaloy, and for further investigations on the correlation between local fuel-cladding bonding and stress corrosion cracking

Performance of Nb protective diffusion coating on U-Mo/Al dispersion fuel

Energy Technology Data Exchange (ETDEWEB)

Kim, Ji-Hyeon; Sohn, Dong-Seong [Ulsan National Institute of Science and Technology, Ulsan (Korea, Republic of); Kim, Sunghwan; Nam, Ji Min; Lee, Kyu Hong; Park, Jong Man [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2014-10-15

To achieve this aim, it is necessary to increase the volume fraction of fuel particles inside the meat. However, the technical limit is reached at approximately 55 vol.% of fuel particles in the aluminum matrix. As a solution, an uranium compound with an higher uranium density than existing U3Si2 fuel has to be selected. Also alloying the uranium must stabilize γ-phase of uranium at room temperature because adequate properties of the γ -phase of uranium showed a good irradiation behavior in the past. Hence, U-Mo alloys were selected as the best candidates. The formation of interaction phase is a critical problem to apply U-Mo alloys to the high performance research reactor. Different means have been proposed to reduce the interaction between U-Mo fuel and Al matrix. There are three means. : 1. Addition of a diffusion limiting element to the matrix 2. Insertion of a diffusion barrier at the interface between the U-Mo and the Al 3. Alloying of the U-Mo with a third element Here we present the effect of Nb coating as diffusion barrier on formation of interaction layers between UMo powders and Al matrix. We present the effect of Nb coating on formation of interaction layers between U-Mo powders and Al matrix. Centrifugally atomized U-7 wt.% Mo powders were used, and Nb was coated on the surface of U-7 wt.% Mo by sputtering. Subsequently, the Nb-coated U-7 wt.% Mo powders were mixed with pure Al powders, and were made into compacts. The compacts were annealed at 550 .deg. C for 1, 3, 5 hours, respectively, and the result showed that the Nb coating on U-7 wt.% Mo effectively suppressed the growth of interaction layers between U-7 wt.% Mo and Al matrix.

Fluorine and chlorine determination in mixed uranium-plutonium oxide fuel and plutonium dioxide

International Nuclear Information System (INIS)

Elinson, S.V.; Zemlyanukhina, N.A.; Pavlova, I.V.; Filatkina, V.P.; Tsvetkova, V.T.

1981-01-01

A technique of fluorine and chlorine determination in the mixed uranium-plutonium oxide fuel and plutonium dioxide, based on their simultaneous separation by means of pyrohydrolysis, is developed. Subsequently, fluorine is determined by photometry with alizarincomplexonate of lanthanum or according to the weakening of zirconium colouring with zylenol orange. Chlorine is determined using the photonephelometric method according to the reaction of chloride-ion interaction with silver nitrate or by spectrophotometric method according to the reaction with mercury rhodanide. The lower limit of fluorine determination is -6x10 -5 %, of chlorine- 1x10 -4 % in the sample of 1g. The relative mean quadratic deviation of the determination result (Ssub(r)), depends on the character of the material analyzed and at the content of nx10 -4 - nx10 -3 mass % is equal to from 0.05 to 0.32 for fluorine and from 0.11 to 0.35 for chlorine [ru

The development of CVR coatings for PBR fuels

Science.gov (United States)

Barletta, R. E.; Vanier, P. E.; Dowell, M. B.; Lennartz, J. A.

Particle bed reactors (PBR's) are being developed for both space power and propulsion applications. These reactors operate with exhaust gas temperatures of 2500 to 3000 K and fuel temperatures hundreds of degrees higher. One fuel design for these reactors consists of uranium carbide encapsulated in either carbon or graphite. This fuel kernel must be protected from the coolant gas, usually H2, both to prevent attack of the kernel and to limit fission product release. Refractory carbide coatings have been proposed for this purpose. The typical coating process used for this is a chemical vapor deposition. Testing of other components have indicated the superiority of refractory carbide coatings applied using a chemical vapor reaction (CVR) process, however technology to apply these coatings to large numbers of fuel particles with diameters on the order of 500 pm were not readily available. A process to deposit these CVR coatings on surrogate fuel consisting of graphite particles is described. Several types of coatings have been applied to the graphite substrate: NbC in various thicknesses and a bilayer coating consisting of NbC and TaC with a intermediate layer of pyrolytic graphite. These coated particles have been characterized prior to test; results are presented.

Corrosion testing of uranium silicide fuel specimens

International Nuclear Information System (INIS)

Bourns, W.T.

1968-09-01

U 3 Si is the most promising high density natural uranium fuel for water-cooled power reactors. Power reactors fuelled with this material are expected to produce cheaper electricity than those fuelled with uranium dioxide. Corrosion tests in 300 o C water preceded extensive in-reactor performance tests of fuel elements and bundles. Proper heat-treatment of U-3.9 wt% Si gives a U 3 5i specimen which corrodes at less than 2 mg/cm 2 h in 300 o C water. This is an order of magnitude lower than the maximum corrosion rate tolerable in a water-cooled reactor. U 3 Si in a defected unbonded Zircaloy-2 sheath showed only a slow uniform sheath expansion in 300 o C water. All tests were done under isothermal conditions in an out-reactor loop. (author)

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.

Conversion of highly enriched uranium in thorium-232 based oxide fuel for light water reactors: MOX-T fuel

Energy Technology Data Exchange (ETDEWEB)

Vapirev, E; Jordanov, T; Khristoskov, I [Sofia Univ. (Bulgaria). Fizicheski Fakultet

1996-12-31

The possibility of using highly enriched uranium available from military inventories for production of mixed oxide fuel (MOX) has been proposed. The fuel is based on U-235 dioxide as fissile isotope and Th-232 dioxide as a non-fissile isotope. It is shown that although the fuel conversion coefficient to U-233 is expected to be less than 1, the proposed fuel has several important advantages resulting in cost reduction of the nuclear fuel cycle. The expected properties of MOX fuel (cross-sections, generated chains, delayed neutrons) are estimated. Due to fuel generation the initial enrichment is expected to be 1% less for production of the same energy. In contrast to traditional fuel no long living actinides are generated which reduces the disposal and reprocessing cost. 7 refs.

Uranium dispersion in the coating of weak-acid-resin-deprived HTGR fuel microspheres

International Nuclear Information System (INIS)

Weber, G.W.; Beatty, R.L.; Tennery, V.J.; Lackey, W.J. Jr.

1976-02-01

The current reference HTGR recycle fuel particle is a UO 2 /UC 2 kernel with a Triso coating comprising a low-density pyrocarbon (PyC) buffer, a high-density PyC inner LTI coating, SiC, and a high-density PyC outer LTI. The kernel is fabricated from a weak-acid ion exchange resin (WAR). Microradiographic examination of coated WAR particles has demonstrated that considerable U can be transferred from the kernel to the buffer coating during fabrication. Investigation of causes of fuel dispersion has indicated several different factors that contribute to fuel redistribution if not properly controlled. The presence of a nonequilibrium UC/sub 1-x/O/sub x/ (0 less than or equal to x less than or equal to 0.3) phase had no significant effect on initiating fuel dispersion. Gross exposure of the completed fuel kernel to ambient atmosphere or to water vapor at room temperature produced very minimal levels of dispersion. Exposure of the fuel to perchloroethylene during buffer and inner LTI deposition produced massive redistribution. Fuel redistribution observed in Triso-coated particles results from permeation of the inner LTI by HCl during SiC deposition. As the decomposition of CH 3 Cl 3 Si is used to deposit SiC, chlorine is readily available during this process. The permeability of the inner LTI coating has a marked effect on the extent of this mode of fuel dispersion. LTI permeability was determined by chlorine leaching studies to be a strong function of density, coating gas dilution, and coating temperature but relatively unaffected by application of a seal coat, variations in coating thickness, and annealing at 1800 0 C. Mechanical attrition of the kernels during processing was identified as a potential source of U-bearing fines that may be incorporated into the coating in some circumstances

Dissolution of uranium dioxide in supercritical carbon dioxide modified with tri-n-butyl phosphate-hydrogen peroxide

International Nuclear Information System (INIS)

Kanekar, A.S.; Pathak, P.N.; Mohapatra, P.K.; Manchanda, V.K.

2009-01-01

Direct dissolution of uranium dioxide in supercritical carbon dioxide modified with tri-n-butyl phosphate (TBP) has been attempted. The effects of TBP concentration and pressure on the extraction of uranium have been studied. Addition of hydrogen peroxide in the modifier enhances the dissolution/extraction of uranium. (author)

METHOD OF PROTECTIVELY COATING URANIUM

Science.gov (United States)

Eubank, L.D.; Boller, E.R.

1959-02-01

A method is described for protectively coating uranium with zine comprising cleaning the U for coating by pickling in concentrated HNO/sub 3/, dipping the cleaned U into a bath of molten zinc between 430 to 600 C and containing less than 0 01% each of Fe and Pb, and withdrawing and cooling to solidify the coating. The zinccoated uranium may be given a; econd coating with another metal niore resistant to the corrosive influences particularly concerned. A coating of Pb containing small proportions of Ag or Sn, or Al containing small proportions of Si may be applied over the zinc coatings by dipping in molten baths of these metals.

Uranium dioxide. Sintering test

International Nuclear Information System (INIS)

Anon.

Description of a sintering method and of the equipment devoted to uranium dioxide powder caracterization and comparison between different samples. Determination of the curve giving specific volume versus pressure and micrographic examination of a pellet at medium pressure [fr

Effect of additives on enhanced sintering and grain growth in uranium dioxide

International Nuclear Information System (INIS)

Bourgeois, L.

1992-06-01

The use of sintering additives has been the most effective way of promoting grain growth of uranium dioxide. We have established a same mechanism for additives which belongs to corundum structure: chromium, aluminium, vanadium and titanium sesquioxides. Study of thermodynamical stabilities of dopants has lead to define suitable sintering atmospheres in order to enhance grain growth. Low solubility limits have been defined at T=1700 deg C for four additives, from variations of final grain size versus initial dopant concentration Identification of second phase after cooling has been done from electronic diffraction patterns. It appears that these solubilities decrease sharply as positive deviation from stoichiometry of uranium dioxide increases. Dilatometric analysis of sintering of doped uranium dioxide has shown in certain cases some enhancement in densification rates, at the point of onset of abnormal grain growth, which is believed to be the source. Nevertheless, the following growth is accompanied with pores coalescence mechanisms and pores entrapment inside grains. Increased thermal stability, during standard annealing, is expected, limiting thereby redensification of nuclear fuel in reactors. Finally, from investigations of additives vaporizations, Al 2 O 3 and Cr 2 O 3 , oxygen exchanges between additives and matrix are believed to occur, which should lead to enhance pore mobility. (Author)., refs., figs., tabs

Corrosion testing of uranium silicide fuel specimens

Energy Technology Data Exchange (ETDEWEB)

Bourns, W T

1968-09-15

U{sub 3}Si is the most promising high density natural uranium fuel for water-cooled power reactors. Power reactors fuelled with this material are expected to produce cheaper electricity than those fuelled with uranium dioxide. Corrosion tests in 300{sup o}C water preceded extensive in-reactor performance tests of fuel elements and bundles. Proper heat-treatment of U-3.9 wt% Si gives a U{sub 3}5i specimen which corrodes at less than 2 mg/cm{sup 2} h in 300{sup o}C water. This is an order of magnitude lower than the maximum corrosion rate tolerable in a water-cooled reactor. U{sub 3}Si in a defected unbonded Zircaloy-2 sheath showed only a slow uniform sheath expansion in 300{sup o}C water. All tests were done under isothermal conditions in an out-reactor loop. (author)

NARCISS critical stand experiments for studying the nuclear safety in accident water immersion of highly enriched uranium dioxide fuel elements

International Nuclear Information System (INIS)

Ponomarev-Stepnoj, N.N.; Glushkov, E.S.; Bubelev, V.G.

2005-01-01

A brief description of the Topaz-2 SNPS designed under scientific supervision of RRC KI in Russia, and of the NARCISS critical facility, is given. At the NARCISS critical facility, neutronic peculiarities and nuclear safety issues of the Topaz-2 system reactor were studied experimentally. This work is devoted to a detailed description of experiments on investigation of criticality safety in accident water immersion og highly enriched uranium dioxide fuel elements, performed at the NARCISS facility. The experiments were carried out at water-moderated critical assemblies with varying height, number, and spacing of fuel elements. The results obtained in the critical experiments, computational models of the investigated critical configurations, and comparison of the computational and experimental results are given [ru

Interaction of Al2O3xSiO2 alloyed uranium oxide with pyrocarbon coating of fuel particles under irradiation

International Nuclear Information System (INIS)

Chernikov, A.S.; Khromov, Yu.F.; Svistunov, D.E.; Chujko, E.E.

1989-01-01

Method of comparative data analysis for P O2 and P CO was used to consider interaction in fuel particle between pyrocarbon coating and fuel sample, alloyed with alumosilicate addition. Equations of interaction reactions for the case of hermetic and depressurized fuel particle are presented. Calculations of required xAl 2 O 3 XySiO 2 content, depending on oxide fuel burnup, were conducted. It was suggested to use silicon carbide for limitation of the upper level of CO pressure in fuel particle. Estimation of thermal stability of alumosilicates under conditions of uranium oxide burnup equals 1100 and 1500 deg C for Al/Si ratio in addition 1/1 and 4/1 respectively

Yellow cake to ceramic uranium dioxide

International Nuclear Information System (INIS)

Zawidzki, T.W.; Itzkovitch, I.J.

1983-01-01

This overview article first reviews the processes for converting uranium ore concentrates to ceramic uranium dioxide at the Port Hope Refinery of Eldorado Resources Limited. In addition, some of the problems, solutions, thoughts and research direction with respect to the production and properties of ceramic UO 2 are described

Inert matrix fuel in dispersion type fuel elements

Energy Technology Data Exchange (ETDEWEB)

Savchenko, A.M. [A.A. Bochvar All-Russia Research Institute of Inorganic Materials (VNIINM) 123060, P.O. Box 369, Rogova Street, 5A, Moscow (Russian Federation)]. E-mail: sav@bochvar.ru; Vatulin, A.V. [A.A. Bochvar All-Russia Research Institute of Inorganic Materials (VNIINM) 123060, P.O. Box 369, Rogova Street, 5A, Moscow (Russian Federation); Morozov, A.V. [A.A. Bochvar All-Russia Research Institute of Inorganic Materials (VNIINM) 123060, P.O. Box 369, Rogova Street, 5A, Moscow (Russian Federation); Sirotin, V.L. [A.A. Bochvar All-Russia Research Institute of Inorganic Materials (VNIINM) 123060, P.O. Box 369, Rogova Street, 5A, Moscow (Russian Federation); Dobrikova, I.V. [A.A. Bochvar All-Russia Research Institute of Inorganic Materials (VNIINM) 123060, P.O. Box 369, Rogova Street, 5A, Moscow (Russian Federation); Kulakov, G.V. [A.A. Bochvar All-Russia Research Institute of Inorganic Materials (VNIINM) 123060, P.O. Box 369, Rogova Street, 5A, Moscow (Russian Federation); Ershov, S.A. [A.A. Bochvar All-Russia Research Institute of Inorganic Materials (VNIINM) 123060, P.O. Box 369, Rogova Street, 5A, Moscow (Russian Federation); Kostomarov, V.P. [A.A. Bochvar All-Russia Research Institute of Inorganic Materials (VNIINM) 123060, P.O. Box 369, Rogova Street, 5A, Moscow (Russian Federation); Stelyuk, Y.I. [A.A. Bochvar All-Russia Research Institute of Inorganic Materials (VNIINM) 123060, P.O. Box 369, Rogova Street, 5A, Moscow (Russian Federation)

2006-06-30

The advantages of using inert matrix fuel (IMF) as a dispersion fuel in an aluminium alloy matrix are considered, in particular, low temperatures in the fuel centre, achievable high burn-ups, serviceability in transients and an environmentally friendly process of fuel rod fabrication. Two main versions of IMF are under development at A.A. Bochvar Institute, i.e. heterogeneous or isolated distribution of plutonium. The out-of-pile results on IMF loaded with uranium dioxide as plutonium simulator are presented. Fuel elements with uranium dioxide composition fabricated at A.A. Bochvar Institute are currently under MIR tests (RIAR, Dimitrovgrad). The fuel elements reached a burn-up of 88 MW d kg{sup -1} (equivalent to the burn up of the standard uranium dioxide pelletized fuel) without loss of leak-tightness of the cladding. The feasibility of fabricating IMF of these particular types with plutonium dioxide is considered with a view to in-pile irradiation.

Inert matrix fuel in dispersion type fuel elements

Science.gov (United States)

Savchenko, A. M.; Vatulin, A. V.; Morozov, A. V.; Sirotin, V. L.; Dobrikova, I. V.; Kulakov, G. V.; Ershov, S. A.; Kostomarov, V. P.; Stelyuk, Y. I.

2006-06-01

The advantages of using inert matrix fuel (IMF) as a dispersion fuel in an aluminium alloy matrix are considered, in particular, low temperatures in the fuel centre, achievable high burn-ups, serviceability in transients and an environmentally friendly process of fuel rod fabrication. Two main versions of IMF are under development at A.A. Bochvar Institute, i.e. heterogeneous or isolated distribution of plutonium. The out-of-pile results on IMF loaded with uranium dioxide as plutonium simulator are presented. Fuel elements with uranium dioxide composition fabricated at A.A. Bochvar Institute are currently under MIR tests (RIAR, Dimitrovgrad). The fuel elements reached a burn-up of 88 MW d kg-1 (equivalent to the burn up of the standard uranium dioxide pelletized fuel) without loss of leak-tightness of the cladding. The feasibility of fabricating IMF of these particular types with plutonium dioxide is considered with a view to in-pile irradiation.

The uranium fuel cycle at IPEN - Energy and Nuclear Research Institute, SP, Brazil

International Nuclear Information System (INIS)

Abrao, Alcidio

1994-09-01

This paper summarizes the progress of research concerning the uranium fuel cycle set up at the IPEN, Sao Paulo, from the raw yellow-cake to the uranium hexafluoride. It covers the reconversion of the hexafluoride to ammonium uranyl tricarbonate and the manufacturing of the fuel elements for the swimming pool IEA-R1 reactor. This review extends the coverage of two pilot plants for uranium purification based upon ion exchange, one demonstration unity for the purification of uranyl nitrate by solvent extraction in pulsed columns, the unity of uranium tetrafluoride into moving bed reactors and a second one based upon the wet chemistry via uranium dioxide and aqueous hydrogen fluoride. The paper mentions the pilot plant for the preparation of uranium trioxide by the thermal decomposition of ammonium diuranate and a second unity by the thermal denitration of uranyl nitrate. The paper outlines the fluorine plant and the unity for the hexafluoride preparation, the unity for the conversion of the hexa to the ammonium uranyl tricarbonate and the fabrication of fuel elements for the IEA-R1 reactor. (author)

Thermal properties of nonstoichiometry uranium dioxide

Science.gov (United States)

Kavazauri, R.; Pokrovskiy, S. A.; Baranov, V. G.; Tenishev, A. V.

2016-04-01

In this paper, was developed a method of oxidation pure uranium dioxide to a predetermined deviation from the stoichiometry. Oxidation was carried out using the thermogravimetric method on NETZSCH STA 409 CD with a solid electrolyte galvanic cell for controlling the oxygen potential of the environment. 4 samples uranium oxide were obtained with a different ratio of oxygen-to-metal: O / U = 2.002, O / U = 2.005, O / U = 2.015, O / U = 2.033. For the obtained samples were determined basic thermal characteristics of the heat capacity, thermal diffusivity, thermal conductivity. The error of heat capacity determination is equal to 5%. Thermal diffusivity and thermal conductivity of the samples decreased with increasing deviation from stoichiometry. For the sample with O / M = 2.033, difference of both values with those of stoichiometric uranium dioxide is close to 50%.

Protective Coatings for Wet Storage of Aluminium-Clad Spent Fuel

Energy Technology Data Exchange (ETDEWEB)

Fernandes, S.M.C.; Correa, O.V.; Souza, J.A. De; Ramanathan, L.V. [Materials science and Technology Center, Instituto de Pesquisas Energeticas e Nucleares - IPEN, Av. Prof. Lineu Prestes 2242, Cidade Universitaria, 05508-000 Sao Paulo (Brazil)

2011-07-01

Corrosion protection of spent RR fuel for long term wet storage was considered important, primarily from the safety standpoint and the use of conversion coatings was proposed in 2008. This paper presents the results of: (a) on-going field tests in which un-coated and lanthanide-based conversion coated Al alloy coupons were exposed to the IEA-R1 reactor spent fuel basin for durations of up to a year; (b) preparation of cerium modified hydrotalcite coatings and cerium sealed boehmite coatings on AA 6061 alloy; (c) corrosion resistance of coated specimens in NaCl solutions. The field studies indicated that the oxidized and cerium dioxide coated coupons were the most corrosion resistant. The cerium modified hydrotalcite and cerium sealed boehmite coated specimens showed marked increase in pitting corrosion resistance. (author)

Nuclear energy - Determination of chlorine and fluorine in uranium dioxide powder and sintered pellets

International Nuclear Information System (INIS)

2008-01-01

This International Standard describes a method for determining the chlorine and fluorine concentrations in uranium dioxide and in sintered fuel pellets by pyrohydrolysis of samples, followed either by liquid ion-exchange chromatography or by selective electrode measurement of chlorine and fluorine ions. Many ion-exchange chromatography systems and ion-selective electrode measurement systems are available

Nitride Coating Effect on Oxidation Behavior of Centrifugally Atomized U-Mo Fuel

Energy Technology Data Exchange (ETDEWEB)

Jeong, Yong Jin; Cho, Woo Hyoung; Park, Jong Man; Lee, Yoon Sang; Yang, Jae Ho [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2011-10-15

Uranium metal and uranium compounds are being used as nuclear fuel materials and generally known as pyrophoric materials. Nowadays the importance of nuclear fuel about safety is being emphasized due to the vigorous exchanges and co-operations among the international community. According to the reduced enrichment for research and test reactors (RERTR) program, the international research reactor community has decided to use low-enriched uranium instead of high-enriched uranium. As a part of the RERTR program, KAERI has developed centrifugally atomized U-Mo alloys as a promising candidate of research reactor fuel. Kang et al. studied the oxidation behavior of centrifugally atomized U-10wt% Mo alloy and it showed better oxidation resistance than uranium. In this study, the oxidation behavior of nitride coated U-7wt% Mo alloy is investigated to enhance the safety against pyrophoricity

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

Reduction of uranium in disposal conditions of spent nuclear fuel

International Nuclear Information System (INIS)

Myllykylae, E.

2008-02-01

This literature study is a summary of publications, in which the reduction of uranium by iron has been investigated in anaerobic groundwater conditions or in aqueous solution in general. The basics of the reduction phenomena and the oxidation states, complexes and solubilities of uranium and iron in groundwaters are discussed as an introduction to the subject, as well as, the Finnish disposal concept of spent nuclear fuel. The spent fuel itself mainly (∼96 %) consists of a sparingly soluble uranium(IV) dioxide, UO 2 (s), which is stable phase in the anticipated reducing disposal conditions. If spent fuel gets in contact with groundwater, oxidizing conditions might be induced by the radiolysis of water, or by the intrusion of oxidizing glacial melting water. Under these conditions, the oxidation and dissolution of uranium dioxide to more soluble U(VI) species could occur. This could lead to the mobilization of uranium and other components of spent fuel matrix including fission products and transuranium elements. The reduction of uranium back to oxidation state U(IV) can be considered as a favourable immobilization mechanism in a long-term, leading to precipitation due to the low solubility of U(IV) species. The cast iron insert of the disposal canister and its anaerobic corrosion products are the most important reductants under disposal conditions, but dissolved ferrous iron may also function as reductant. Other iron sources in the buffer or near-field rock, are also considered as possible reductants. The reduction of uranium is a very challenging phenomenon to investigate. The experimental studies need e.g. well-controlled anoxic conditions and measurements of oxidation states. Reduction and other simultaneous phenomena are difficult to distinghuish. The groundwater conditions (pH, Eh and ions) influence on the prevailing complexes of U and Fe and on forming corrosion products of iron and, thus they determine also the redox chemistry. The partial reduction of

Contribution to the study of second phases particles dispersion in polycrystalline uranium dioxide

International Nuclear Information System (INIS)

Peres, V.

1994-06-01

To reduce fission gas release of irradiated polycrystalline uranium dioxide, the dispersion of intragranular nanometric particles of second phase necessary to pin gas bubbles may complete the advantage of a large-grained fuel microstructure. Moreover, intergranular glass films may improve high temperatures mechanical properties of UO 2 . In this study, mixtures of additives composed of ''corindon'' structure oxides that enhance the fuel grain growth and composed of different oxides with variable solid solubilities in the UO 2 matrix were achieved. Additives with a negligible solubility inhibit grain boundaries motion except those, such as silica, that involve a liquid phase at the sintering temperature. Rare earth oxides that form stable solid solutions with UO 2 cannot lead to precipitation, but have no effect on the fuel grain growth doped with ''corindon'' type oxides. A chromium oxide excess allows the creation of a fuel microstructure described by large grains and intragranular spherical Cr 2 O 3 inclusions observed by scanning electron microscopy. Values for the bulk lattice diffusion coefficient of Cr 3+ cations in UO 2 can be deduced from the experimental growth of those dispersed particles by an Ostwald ripening mechanism. The formation of small precipitated metal particles inside the uranium dioxide matrix induced by the internal reduction of a solid solution has not been performed. However, direct reduction of insoluble chromium oxide particles is easy and produces metallic intragranular precipitates. (author). 119 refs., 112 figs., 33 tabs., 5 annexes

Uranium tetrafluoride production via dioxide by wet process

International Nuclear Information System (INIS)

Aquino, A.R. de.

1988-01-01

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

Coated U(Mo) Fuel: As-Fabricated Microstructures

Energy Technology Data Exchange (ETDEWEB)

Emmanuel Perez; Dennis D. Keiser, Jr.; Ann Leenaers; Sven Van den Berghe; Tom Wiencek

2014-04-01

As part of the development of low-enriched uranium fuels, fuel plates have recently been tested in the BR-2 reactor as part of the SELENIUM experiment. These fuel plates contained fuel particles with either Si or ZrN thin film coating (up to 1 µm thickness) around the U-7Mo fuel particles. In order to best understand irradiation performance, it is important to determine the starting microstructure that can be observed in as-fabricated fuel plates. To this end, detailed microstructural characterization was performed on ZrN and Si-coated U-7Mo powder in samples taken from AA6061-clad fuel plates fabricated at 500°C. Of interest was the condition of the thin film coatings after fabrication at a relatively high temperature. Both scanning electron microscopy and transmission electron microscopy were employed. The ZrN thin film coating was observed to consist of columns comprised of very fine ZrN grains. Relatively large amounts of porosity could be found in some areas of the thin film, along with an enrichment of oxygen around each of the the ZrN columns. In the case of the pure Si thin film coating sample, a (U,Mo,Al,Si) interaction layer was observed around the U-7Mo particles. Apparently, the Si reacted with the U-7Mo and Al matrix during fuel plate fabrication at 500°C to form this layer. The microstructure of the formed layer is very similar to those that form in U-7Mo versus Al-Si alloy diffusion couples annealed at higher temperatures and as-fabricated U-7Mo dispersion fuel plates with Al-Si alloy matrix fabricated at 500°C.

Investigation of the dissolution of uranium dioxide in nitric media: a new approach aiming at understanding interface mechanisms

International Nuclear Information System (INIS)

Delwaulle, Celine

2011-01-01

This research thesis deals with the back-end cycle of the nuclear fuel by improving, modernizing and optimizing the processes used for all types of fuels which are to be re-processed. After a presentation of the industrial context and of the state of the art concerning dissolution kinetic data for uranium dioxide and mixed oxide, the author proposes a model which couples dissolution kinetics and hydrodynamics of a solid in presence of auto-catalytic species, in order to better understand phenomena occurring at the solid-liquid-gas interface. The next part reports dissolution experiments on a non-radioactive material (copper) and out of a nuclear environment. Then, the author identifies steps which are required to transpose this experiment within a nuclear environment. The first results obtained on uranium dioxide are discussed. Recommendations for further studies conclude the report

Uranium production in thorium/denatured uranium fueled PWRs

International Nuclear Information System (INIS)

Arthur, W.B.

1977-01-01

Uranium-232 buildup in a thorium/denatured uranium fueled pressurized water reactor, PWR(Th), was studied using a modified version of the spectrum-dependent zero dimensional depletion code, LEOPARD. The generic Combustion Engineering System 80 reactor design was selected as the reactor model for the calculations. Reactors fueled with either enriched natural uranium and self-generated recycled uranium or uranium from a thorium breeder and self-generated recycled uranium were considered. For enriched natural uranium, concentrations of 232 U varied from about 135 ppM ( 232 U/U weight basis) in the zeroth generation to about 260 ppM ( 232 U/U weight basis) at the end of the fifth generation. For the case in which thorium breeder fuel (with its relatively high 232 U concentration) was used as reactor makeup fuel, concentrations of 232 U varied from 441 ppM ( 232 U/U weight basis) at discharge from the first generation to about 512 ppM ( 232 U/U weight basis) at the end of the fifth generation. Concentrations in freshly fabricated fuel for this later case were 20 to 35% higher than the discharge concentration. These concentrations are low when compared to those of other thorium fueled reactor types (HTGR and MSBR) because of the relatively high 238 U concentration added to the fuel as a denaturant. Excellent agreement was found between calculated and existing experimental values. Nevertheless, caution is urged in the use of these values because experimental results are very limited, and the relevant nuclear data, especially for 231 Pa and 232 U, are not of high quality

Process for the preparation of uranium dioxide

International Nuclear Information System (INIS)

Watt, G.W.; Baugh, D.W. Jr.

1981-01-01

A method for the preparation of actinide dioxides using actinide nitrate hexahydrates as starting materials is described. The actinide nitrate hexahydrate is reacted with sodium dithionite, and the product is heated in the absence of oxygen to obtain the dioxide. Preferably, the actinide is uranium, plutonium or neptunium. (LL)

Fabrication of Uranium Oxycarbide Kernels for HTR Fuel

International Nuclear Information System (INIS)

Barnes, Charles; Richardson, Clay; Nagley, Scott; Hunn, John; Shaber, Eric

2010-01-01

Babcock and Wilcox (B and W) has been producing high quality uranium oxycarbide (UCO) kernels for Advanced Gas Reactor (AGR) fuel tests at the Idaho National Laboratory. In 2005, 350-(micro)m, 19.7% 235U-enriched UCO kernels were produced for the AGR-1 test fuel. Following coating of these kernels and forming the coated-particles into compacts, this fuel was irradiated in the Advanced Test Reactor (ATR) from December 2006 until November 2009. B and W produced 425-(micro)m, 14% enriched UCO kernels in 2008, and these kernels were used to produce fuel for the AGR-2 experiment that was inserted in ATR in 2010. B and W also produced 500-(micro)m, 9.6% enriched UO2 kernels for the AGR-2 experiments. Kernels of the same size and enrichment as AGR-1 were also produced for the AGR-3/4 experiment. In addition to fabricating enriched UCO and UO2 kernels, B and W has produced more than 100 kg of natural uranium UCO kernels which are being used in coating development tests. Successive lots of kernels have demonstrated consistent high quality and also allowed for fabrication process improvements. Improvements in kernel forming were made subsequent to AGR-1 kernel production. Following fabrication of AGR-2 kernels, incremental increases in sintering furnace charge size have been demonstrated. Recently small scale sintering tests using a small development furnace equipped with a residual gas analyzer (RGA) has increased understanding of how kernel sintering parameters affect sintered kernel properties. The steps taken to increase throughput and process knowledge have reduced kernel production costs. Studies have been performed of additional modifications toward the goal of increasing capacity of the current fabrication line to use for production of first core fuel for the Next Generation Nuclear Plant (NGNP) and providing a basis for the design of a full scale fuel fabrication facility.

Thermochemical equilibrium in a kernel of a UN TRISO coated fuel particle

International Nuclear Information System (INIS)

Kim, Young Min; Jo, C. K.; Lim, H. S.; Cho, M. S.; Lee, W. J.

2012-01-01

A coated fuel particle (CFP) with a uranium mononitride (UN) kernel has been recently considered as an advanced fuel option, such as in fully ceramic micro encapsulated (FCM) replacement fuel for light water reactors (LWRs). In FCM fuel, a large number of tri isotropic coated fuel particles (TRISOs) are embedded in a silicon carbide (SiC) matrix. Thermochemical equilibrium calculations can predict the chemical behaviors of a kernel in a TRISO of FCM fuel during irradiation. They give information on the kind and quantity of gases generated in a kernel during irradiation. This study treats the quantitative analysis of thermochemical equilibrium in a UN TRISO of FCM LWR fuel using HSC software

Thermal conductivity of uranium dioxide

International Nuclear Information System (INIS)

Pillai, C.G.S.; George, A.M.

1993-01-01

The thermal conductivity of uranium dioxide of composition UO 2.015 was measured from 300 to 1400 K. The phonon component of the conductivity is found to be quantitatively accounted for by the theoretical expression of Slack derived by modifying the Leibfried-Schlomann equation. (orig.)

Electronic structure calculations of atomic transport properties in uranium dioxide: influence of strong correlations

International Nuclear Information System (INIS)

Dorado, B.

2010-09-01

Uranium dioxide UO 2 is the standard nuclear fuel used in pressurized water reactors. During in-reactor operation, the fission of uranium atoms yields a wide variety of fission products (FP) which create numerous point defects while slowing down in the material. Point defects and FP govern in turn the evolution of the fuel physical properties under irradiation. In this study, we use electronic structure calculations in order to better understand the fuel behavior under irradiation. In particular, we investigate point defect behavior, as well as the stability of three volatile FP: iodine, krypton and xenon. In order to take into account the strong correlations of uranium 5f electrons in UO 2 , we use the DFT+U approximation, based on the density functional theory. This approximation, however, creates numerous metastable states which trap the system and induce discrepancies in the results reported in the literature. To solve this issue and to ensure the ground state is systematically approached as much as possible, we use a method based on electronic occupancy control of the correlated orbitals. We show that the DFT+U approximation, when used with electronic occupancy control, can describe accurately point defect and fission product behavior in UO 2 and provide quantitative information regarding point defect transport properties in the oxide fuel. (author)

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

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

International Nuclear Information System (INIS)

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

1991-01-01

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

Nuclear energy - Uranium dioxide powder and sintered pellets - Determination of oxygen/uranium atomic ratio by the amperometric method. 2. ed.

International Nuclear Information System (INIS)

2007-01-01

This International Standard specifies an analytical method for the determination of the oxygen/uranium atomic ratio in uranium dioxide powder and sintered pellets. The method is applicable to reactor grade samples of hyper-stoichiometric uranium dioxide powder and pellets. The presence of reducing agents or residual organic additives invalidates the procedure. The test sample is dissolved in orthophosphoric acid, which does not oxidize the uranium(IV) from UO 2 molecules. Thus, the uranium(VI) that is present in the dissolved solution is from UO 3 and/or U 3 O 8 molecules only, and is proportional to the excess oxygen in these molecules. The uranium(VI) content of the solution is determined by titration with a previously standardized solution of ammonium iron(II) sulfate hexahydrate in orthophosphoric acid. The end-point of the titration is determined amperometrically using a pair of polarized platinum electrodes. The oxygen/uranium ratio is calculated from the uranium(VI) content. A portion, weighing about 1 g, of the test sample is dissolved in orthophosphoric acid. The dissolution is performed in an atmosphere of nitrogen or carbon dioxide when sintered material is being analysed. When highly sintered material is being analysed, the dissolution is performed at a higher temperature in purified phosphoric acid from which the water has been partly removed. The cooled solution is titrated with an orthophosphoric acid solution of ammonium iron(II) sulfate, which has previously been standardized against potassium dichromate. The end-point of the titration is detected by the sudden increase of current between a pair of polarized platinum electrodes on the addition of an excess of ammonium iron(II) sulfate solution. The paper provides information about scope, principle, reactions, reagents, apparatus, preparation of test sample, procedure (uranium dioxide powder, sintered pellets of uranium dioxide, highly sintered pellets of uranium dioxide and determination

Mechanical Properties and Structures of Pyrolytic Carbon Coating Layer in HTR Coated Particle Fuel

International Nuclear Information System (INIS)

Lee, Young Woo; Kim, Young Min; Kim, Woong Ki; Cho, Moon Sung

2009-01-01

The TRISO(tri-isotropic)-coated fuel particle for a HTR(High Temperature gas-cooled Reactor) has a diameter of about 1 mm, composed of a nuclear fuel kernel and four different outer coating layers, consisting of a buffer PyC (pyrolytic carbon) layer, inner PyC layer, SiC layer, and outer PyC layer with different coating thicknesses following a specific fuel design. While the fuel kernel is a source for a heat generation by a nuclear fission of fissile uranium, each of the four coating layers acts as a different role in view of retaining the generated fission products and the other interactions during an in-reactor service. Among these coating layers, PyC properties are scarcely in agreement among various investigators and the dependency of their changes upon the deposition condition is comparatively large due to their additional anisotropic properties. Although a recent review work has contributed to an establishment of relationship between the material properties and QC measurements, the data on the mechanical properties and structural parameters of PyC coating layers remain still unclearly evaluated. A review work on dimensional changes of PyC by neutron irradiation was one of re-evaluative works recently attempted by the authors. In this work, an attempt was made to analyze and re-evaluate the existing data of the experimental results of the mechanical properties, i.e., Young's modulus and fracture stress, in relation with the coating conditions, density and the BAF (Bacon Anisotropy Factor), an important structural parameter, of PyC coating layers obtained from various experiments performed in the early periods of the HTR coated particle development

Immobilization of chlorine dioxide modified cells for uranium absorption

International Nuclear Information System (INIS)

He, Shengbin; Ruan, Binbiao; Zheng, Yueping; Zhou, Xiaobin; Xu, Xiaoping

2014-01-01

There has been a trend towards the use of microorganisms to recover metals from industrial wastewater, for which various methods have been reported to be used to improve microorganism adsorption characteristics such as absorption capacity, tolerance and reusability. In present study, chlorine dioxide(ClO 2 ), a high-efficiency, low toxicity and environment-benign disinfectant, was first reported to be used for microorganism surface modification. The chlorine dioxide modified cells demonstrated a 10.1% higher uranium adsorption capacity than control ones. FTIR analysis indicated that several cell surface groups are involved in the uranium adsorption and cell surface modification. The modified cells were further immobilized on a carboxymethylcellulose (CMC) matrix to improve their reusability. The cell-immobilized adsorbent could be employed either in a high concentration system to move vast UO 2 2+ ions or in a low concentration system to purify UO 2 2+ contaminated water thoroughly, and could be repeatedly used in multiple adsorption-desorption cycles with about 90% adsorption capacity maintained after seven cycles. - Highlights: • Chlorine dioxide was first reported to be used for microorganism surface modification. • The chlorine dioxide modified cells demonstrated a 10.1% higher uranium adsorption capacity than control ones. • The chlorine dioxide modified cells were further immobilized by carboxymethylcellulose to improve their reusability

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)

Design and fabrication of an advanced TRISO fuel with ZrC coating

Energy Technology Data Exchange (ETDEWEB)

Porter, Ian E., E-mail: porteri@email.sc.edu [University of South Carolina, Mechanical Engineering Department, 300 Main Street, Columbia, SC 29208, United Sates (United States); Knight, Travis W., E-mail: knighttw@cec.sc.edu [University of South Carolina, Mechanical Engineering Department, 300 Main Street, Columbia, SC 29208, United Sates (United States); Dulude, Michael C., E-mail: dulude@email.sc.edu [University of South Carolina, Mechanical Engineering Department, 300 Main Street, Columbia, SC 29208, United Sates (United States); Roberts, Elwyn, E-mail: robertse@cec.sc.edu [University of South Carolina, Mechanical Engineering Department, 300 Main Street, Columbia, SC 29208, United Sates (United States); Hobbs, Jim, E-mail: JSHobbs@nuclearfuelservices.com [Nuclear Fuel Services, Inc., 1205 Banner Hill Road, Erwin, TN 37650 (United States)

2013-06-15

Highlights: • Zirconium carbide was deposited on surrogate zirconia and UO{sub 2} kernels. • Deposition rates were found to be dependent on temperature and gas concentration. • Calcining and sintering parameters were optimized to reduce cracking in UO{sub 2} kernel production. -- Abstract: Very high temperature reactors (VHTRs) are expected to achieve coolant outlet temperatures up to 1000 °C, allowing for increased plant efficiency as well as the ability to use the process heat for hydrogen production and various uses in the process chemical industry. The feasibility of using VHTRs as part of the next generation of nuclear reactors greatly depends on the reliability of tri-structural isotropic (TRISO) fuel particles to retain both gaseous and metallic fission products created in irradiated uranium dioxide (UO{sub 2}). This work sought the deposition parameters necessary to produce an additional zirconium carbide (ZrC) layer used in advanced coated particle fuels. The additional ZrC layer will act as an oxygen getter to prevent typical TRISO failure mechanisms including over pressurization of the particle and kernel migration of the kernel within the particle, also known as the amoeba effect. In this study, ZrC coatings were applied to surrogate zirconia kernels as well as UO{sub 2} kernels using a chemical vapor deposition (CVD) fluidized bed reactor, and the deposition characteristics were analyzed via scanning electron microscopy (SEM) techniques. The ZrC layer was confirmed through X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The calcining and sintering of urania kernels for use in these coating experiments is also discussed.

Design and fabrication of an advanced TRISO fuel with ZrC coating

International Nuclear Information System (INIS)

Porter, Ian E.; Knight, Travis W.; Dulude, Michael C.; Roberts, Elwyn; Hobbs, Jim

2013-01-01

Highlights: • Zirconium carbide was deposited on surrogate zirconia and UO 2 kernels. • Deposition rates were found to be dependent on temperature and gas concentration. • Calcining and sintering parameters were optimized to reduce cracking in UO 2 kernel production. -- Abstract: Very high temperature reactors (VHTRs) are expected to achieve coolant outlet temperatures up to 1000 °C, allowing for increased plant efficiency as well as the ability to use the process heat for hydrogen production and various uses in the process chemical industry. The feasibility of using VHTRs as part of the next generation of nuclear reactors greatly depends on the reliability of tri-structural isotropic (TRISO) fuel particles to retain both gaseous and metallic fission products created in irradiated uranium dioxide (UO 2 ). This work sought the deposition parameters necessary to produce an additional zirconium carbide (ZrC) layer used in advanced coated particle fuels. The additional ZrC layer will act as an oxygen getter to prevent typical TRISO failure mechanisms including over pressurization of the particle and kernel migration of the kernel within the particle, also known as the amoeba effect. In this study, ZrC coatings were applied to surrogate zirconia kernels as well as UO 2 kernels using a chemical vapor deposition (CVD) fluidized bed reactor, and the deposition characteristics were analyzed via scanning electron microscopy (SEM) techniques. The ZrC layer was confirmed through X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The calcining and sintering of urania kernels for use in these coating experiments is also discussed

Process for producing uranium oxide rich compositions from uranium hexafluoride

International Nuclear Information System (INIS)

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

1978-01-01

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

New Concept of Designing Composite Fuel for Fast Reactors with Closing Fuel Cycle

International Nuclear Information System (INIS)

Savchenko, A.; Vatulin, A.; Uferov, O.; Kulakov, G.; Sorokin, V.

2013-01-01

For fast reactors a novel type of promising composite U-PuO2 fuel is proposed which is based on dispersion fuel elements. Basic approach to fuel element development - separated operations of fabricating uranium meat fuel element and introducing into it Pu or MA dioxides powder, that results in minimizing dust forming operations in fuel element fabrication. Novel fuel features higher characteristics in comparison to metallic or MOX fuel its fabrication technology is readily accomplished and is environmentally clean. A possibility is demonstrated of fabricating coated steel claddings to protect from interaction with fuel and fission products when use standard rod type MOX or metallic U-Pu-Zr fuel. Novel approach to reprocessing of composite fuel is demonstrated, which allows to separate uranium from burnt plutonium as well as the newly generated fissile plutonium from burnt one without chemical processes, which simplifies the closing of the nuclear fuel cycle. Novel composite fuel combines the advantages of metallic and ceramic types of fuel and has high uranium density that allows also to implicate it in BREST types reactor with conversion ratio more than 1. Peculiarities of closing nuclear cycle with composite fuel are demonstrated that allows more effective re-usage of generated Pu as well as, minimizing r/a wastes by incineration of MA in specially developed IMF design

Study on nano-coating on uranium

International Nuclear Information System (INIS)

Zhang Yongbin; Xian Xiaobin; Lu Xuechao; Lang Dingmu; Li Kexue; Tang Kai

2002-01-01

The SiO 2 , TiO 2 coatings on uranium have been prepared by sol-gel method under different processes. By evaluating the coating quality with SEM, the optimal process parameters have been determined. Corrosion test shows that the coatings have anticorrosion property

1976 scientific progress report. [Fuel and coating materials for HTGR]; Wissenschaftlicher Ergebnisberict 1976

Energy Technology Data Exchange (ETDEWEB)

Nickel, H.

1976-07-01

Activities at the Institute for Reactor Materials in the production and properties of high temperature gas cooled reactor fuel and coating materials are summarized. Major emphasis was placed on investigations of pyrocarbon, BISO and TRISO coatings, uranium and thorium oxides and carbides, and graphite and matrix materials. A list of publications is included. (HDR)

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

A high-temperature, short-duration method of fabricating surrogate fuel microkernels for carbide-based TRISO nuclear fuels

International Nuclear Information System (INIS)

Vasudevamurthy, G.; Radecka, A.; Massey, C.

2015-01-01

High-temperature gas-cooled reactor technology is a frontrunner among generation IV nuclear reactor designs. Among the advanced nuclear fuel forms proposed for these reactors, dispersion-type fuel consisting of microencapsulated uranium di-oxide kernels, popularly known as tri-structural isotropic (TRISO) fuel, has emerged as the fuel form of choice. Generation IV gas-cooled fast reactors offer the benefit of recycling nuclear waste with increased burn-ups in addition to producing the required power and hydrogen. Uranium carbide has shown great potential to replace uranium di-oxide for use in these fast spectrum reactors. Uranium carbide microkernels for fast reactor TRISO fuel have traditionally been fabricated by long-duration carbothermic reduction and sintering of precursor uranium dioxide microkernels produced using sol-gel techniques. These long-duration conversion processes are often plagued by issues such as final product purity and process parameters that are detrimental to minor actinide retention. In this context a relatively simple, high-temperature but relatively quick-rotating electrode arc melting method to fabricate microkernels directly from a feedstock electrode was investigated. The process was demonstrated using surrogate tungsten carbide on account of its easy availability, accessibility and the similarity of its melting point relative to uranium carbide and uranium di-oxide.

A high-temperature, short-duration method of fabricating surrogate fuel microkernels for carbide-based TRISO nuclear fuels

Energy Technology Data Exchange (ETDEWEB)

Vasudevamurthy, G.; Radecka, A.; Massey, C. [Virginia Commonwealth Univ., Richmond, VA (United States). High Temperature Materials Lab.

2015-07-01

High-temperature gas-cooled reactor technology is a frontrunner among generation IV nuclear reactor designs. Among the advanced nuclear fuel forms proposed for these reactors, dispersion-type fuel consisting of microencapsulated uranium di-oxide kernels, popularly known as tri-structural isotropic (TRISO) fuel, has emerged as the fuel form of choice. Generation IV gas-cooled fast reactors offer the benefit of recycling nuclear waste with increased burn-ups in addition to producing the required power and hydrogen. Uranium carbide has shown great potential to replace uranium di-oxide for use in these fast spectrum reactors. Uranium carbide microkernels for fast reactor TRISO fuel have traditionally been fabricated by long-duration carbothermic reduction and sintering of precursor uranium dioxide microkernels produced using sol-gel techniques. These long-duration conversion processes are often plagued by issues such as final product purity and process parameters that are detrimental to minor actinide retention. In this context a relatively simple, high-temperature but relatively quick-rotating electrode arc melting method to fabricate microkernels directly from a feedstock electrode was investigated. The process was demonstrated using surrogate tungsten carbide on account of its easy availability, accessibility and the similarity of its melting point relative to uranium carbide and uranium di-oxide.

DISSOLUTION OF METAL OXIDES AND SEPARATION OF URANIUM FROM LANTHANIDES AND ACTINIDES IN SUPERCRITICAL CARBON DIOXIDE

Energy Technology Data Exchange (ETDEWEB)

Donna L. Quach; Bruce J. Mincher; Chien M. Wai

2013-10-01

This paper investigates the feasibility of extracting and separating uranium from lanthanides and other actinides by using supercritical fluid carbon dioxide (sc-CO2) as a solvent modified with tri-n-butylphosphate (TBP) for the development of a counter current stripping technique, which would be a more efficient and environmentally benign technology for spent nuclear fuel reprocessing compared to traditional solvent extraction. Several actinides (U, Pu, and Np) and europium were extracted in sc-CO2 modified with TBP over a range of nitric acid concentrations and then the actinides were exposed to reducing and complexing agents to suppress their extractability. According to this study, uranium/europium and uranium/plutonium extraction and separation in sc-CO2 modified with TBP is successful at nitric acid concentrations of less than 6 M and at nitric acid concentrations of less than 3 M with acetohydroxamic acid or oxalic acid, respectively. A scheme for recycling uranium from spent nuclear fuel by using sc-CO2 and counter current stripping columns is presented.

Uranium metal and uranium dioxide powder and pellets - Determination of nitrogen content - Method using ammonia-sensing electrode. 1. ed.

International Nuclear Information System (INIS)

1994-01-01

This International Standard specifies an analytical method for determining the nitrogen content in uranium metal and uranium dioxide powder and pellets. It is applicable to the determination of nitrogen, present as nitride, in uranium metal and uranium dioxide powder and pellets. The concentration range within which the method can be used is between 9 μg and 600 μg of nitrogen per gram. Interference can occur from metals which form complex ammines, but these are not normally present in significant amounts

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

Interaction between uranium oxide alloyed with Al2O3·SiO2 and pyrocarbon coating during irradiation of micro fuel elements

International Nuclear Information System (INIS)

Chernikov, A.S.; Khromov, Y.F.; Svistunov, D.E.; Chuiko, E.E.

1989-01-01

The thermodynamics of the interaction between uranium oxide and carbon was previously studied in the presence of Al 2 O 3 ·SiO 2 , SiC, and UC 1.86 ; in this case, the quantity of the reacting substances does not have any effect on the attainment of the equilibrium state. Based on the obtained results, it is interesting to study the characteristic features of the interaction between the alloyed UO x cores (kernels) with the PyC-coating under the conditions involving irradiation of the micro fuel elements with thermal neutrons and the formation of solid fission products. The data concerning the characteristics of a micro fuel element (the weight of the core, its composition, etc.) are useful for carrying out a quantitative evaluation of the additives required for fixing the alkali-earth fission products by obtaining stable compounds of aluminosilicates with Ba, Sr, Rb, and Cs at different levels of depletion (burnup) of the oxide fuel. An analysis of the interaction processes in such a complex system as the irradiated alloyed uranium oxide fuel located in a micro fuel element is carried out by comparing the chemical potential of oxygen (RT ln P O 2 ) for the competing constituents of the system

Uranium tetracyclopentadienyl interaction with carbon oxide and dioxide

International Nuclear Information System (INIS)

Leonov, M.R.; Solov'eva, G.V.; Kozina, I.Z.; Bolotova, G.T.

1983-01-01

Using the methods of gas-liquid chromatography, IR and UV spectroscopy and element analysis, the reactions of tetracyclogentadienyluranium with carbon oxide and dioxide have been studied. It is shown that complete uranium cyclopentadienyl π-complex-tetracyclopentadienyluranium - in pentane under normal conditions for 100 hr reacts with carbon oxide and dioxide with the formation of polymeric complex ([(etasup(5)-Csub(5)Hsub(5))x(-CO-)U(etasup(5)-Csub(5)Hsub(4))(-CO-)]sub(2)]sub(n), in which two uranium atoms are bonded with two bridge fragments (eta 5 -C 5 H 4 -CO-), and dimeric complex [(eta 5 -C 5 H 5 ) 2 UH 2 xCO 2 ] 2 respectively

Production of nuclear ceramic fuel for nuclear power plants at 'Ulba metallurgical plant' OSC

International Nuclear Information System (INIS)

Khadeev, V.G.

2000-01-01

The paper describes the flow-sheet of production of uranium dioxide powders and nuclear ceramic fuel pellets of them existing at the facility. 'UMP' OSC applies ADU extraction process of UO2 powders production. An indisputable success of the process is the possibility of use of the wide range of raw materials. Uranium hexafluoride, uranium oxides, uranium metal, uranium tetrafluoride, uranyl salts, uranium ore concentrates, all possible types of uranium-containing materials the processing of which by routine methods is difficult (ashes, scraps, etc.) are used as the raw materials. In addition, a reprocessed nuclear fuel can be used for fuel production. The quality of uranium dioxide powder produced does not depend on the type of uranium raw material used. High selectivity of extraction refining makes possible to obtain material with rather low impurities content that meets practically all specifications for uranium dioxide known to us. Ceramic and process features of uranium dioxide powders, namely, specific surface, bulk density, grain size and sinterability make possible to produce nuclear ceramic fuel with specified features. Quality of uranium dioxide powders produced by 'UMP' OSC was highly rated by General Electric company that is one of the leading companies from fuel manufactures in the USA market . It has certified 'UMP' OSC as its supplier. Currently, our company makes great efforts on establishing production of uranium dioxide powders with natural isotopes content for production of fuel for CANDU reactors. Trial lots of such powders are under tests at some companies manufacturing fuel for this type reactors in Canada, USA and Corea

Performance Analysis Review of Thorium TRISO Coated Particles during Manufacture, Irradiation and Accident Condition Heating Tests

International Nuclear Information System (INIS)

2015-03-01

Thorium, in combination with high enriched uranium, was used in all early high temperature reactors (HTRs). Initially, the fuel was contained in a kernel of coated particles. However, particle quality was low in the 1960s and early 1970s. Modern, high quality, tristructural isotropic (TRISO) fuel particles with thorium oxide and uranium dioxide (UO 2 ) had been manufactured since 1978 and were successfully demonstrated in irradiation and accident tests. In 1980, HTR fuels changed to low enriched uranium UO 2 TRISO fuels. The wide ranging development and demonstration programme was successful, and it established a worldwide standard that is still valid today. During the process, results of the thorium work with high quality TRISO fuel particles had not been fully evaluated or documented. This publication collects and presents the information and demonstrates the performance of thorium TRISO fuels.This publication is an outcome of the technical contract awarded under the IAEA Coordinated Research Project on Near Term and Promising Long Term Options for Deployment of Thorium Based Nuclear Energy, initiated in 2012. It is based on the compilation and analysis of available results on thorium TRISO coated particle performance in manufacturing and during irradiation and accident condition heating tests

The preparation of uranium tetrafluoride from dioxide by aqueous way

International Nuclear Information System (INIS)

Aquino, A.R. de; Abrao, A.

1990-01-01

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

SPOUTED BED DESIGN CONSIDERATIONS FOR COATED NUCLEAR FUEL PARTICLES

Energy Technology Data Exchange (ETDEWEB)

Marshall, Douglas W.

2017-07-01

High Temperature Gas Cooled Reactors (HTGRs) are fueled with tristructural isotropic (TRISO) coated nuclear fuel particles embedded in a carbon-graphite fuel body. TRISO coatings consist of four layers of pyrolytic carbon and silicon carbide that are deposited on uranium ceramic fuel kernels (350µm – 500µm diameters) in a concatenated series of batch depositions. Each layer has dedicated functions such that the finished fuel particle has its own integral containment to minimize and control the release of fission products into the fuel body and reactor core. The TRISO coatings are the primary containment structure in the HTGR reactor and must have very high uniformity and integrity. To ensure high quality TRISO coatings, the four layers are deposited by chemical vapor deposition (CVD) using high purity precursors and are applied in a concatenated succession of batch operations before the finished product is unloaded from the coating furnace. These depositions take place at temperatures ranging from 1230°C to 1550°C and use three different gas compositions, while the fuel particle diameters double, their density drops from 11.1 g/cm3 to 3.0 g/cm3, and the bed volume increases more than 8-fold. All this is accomplished without the aid of sight ports or internal instrumentation that could cause chemical contamination within the layers or mechanical damage to thin layers in the early stages of each layer deposition. The converging section of the furnace retort was specifically designed to prevent bed stagnation that would lead to unacceptably high defect fractions and facilitate bed circulation to avoid large variability in coating layer dimensions and properties. The gas injection nozzle was designed to protect precursor gases from becoming overheated prior to injection, to induce bed spouting and preclude bed stagnation in the bottom of the retort. Furthermore, the retort and injection nozzle designs minimize buildup of pyrocarbon and silicon carbide on the

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

Investigation of high burnup structures in uranium dioxide applying cellular automata: algorithms and codes

International Nuclear Information System (INIS)

Akishina, E.P.; Kostenko, B.F.; Ivanov, V.V.

2003-01-01

A new method of research in spatial structures that result from uranium dioxide burning in nuclear reactors of modern atomic plants is suggested. The method is based on the presentation of images of the mentioned structures in the form of the working field of a cellular automaton (CA). First, it has allowed one to extract some important quantitative characteristics of the structures directly from the micrographs of the uranium fuel surface. Secondly, the CA has been found out to allow one to formulate easily the dynamics of the evolution of the studied structures in terms of such micrograph elements as spots, spots' boundaries, cracks, etc. Relation has been found between the dynamics and some exactly solvable models of the theory of cellular automata, in particular, the Ising model and the vote model. This investigation gives a detailed description of some CA algorithms which allow one to perform the fuel surface image processing and to model its evolution caused by burnup or chemical etching. (author)

Manufacture of uranium dioxide powder

International Nuclear Information System (INIS)

Becker, M.

1976-01-01

Uranium dioxide powder is prepared by the AUC (ammonium uranyl carbonate) method. Supplementing the known process steps, the AUC, after separation from the mother liquor, is washed with an ammonium hydrogen carbonate or an NH 4 OH solution and is subsequently post-treated with a liquid which reduces the surface tension of the residual water in an AUC. Such a liquid is, for instance, alcohol

Greenhouse gas emissions from the nuclear fuel cycle

International Nuclear Information System (INIS)

Taylor, M.

1996-01-01

Emissions of carbon dioxide and methane from the whole fuel-cycle of nuclear power generation are discussed. The low-cost, and therefore low-energy-using, uranium resources suffice to provide a large worldwide nuclear programme with fuel without producing substantial carbon dioxide. Very lower emissions of carbon dioxide can be achieved if uranium enrichment is carried out by centrifuging. Methane emissions from uranium mining are negligible or in almost any case virtually zero. (author). 9 refs, 1 tab

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)

Hot deformation of polycrystalline uranium dioxide: from microscopic mechanisms to macroscopic behaviour

International Nuclear Information System (INIS)

Dherbey, Francine

2000-01-01

The improvement of nuclear fuels performances in PWR requires in particular an enhancement of creep ability of uranium dioxide in order to minimise rupture risks of the cladding material during interactions between pellets and cladding. The aim of this study is to investigate the link between the ceramic macroscopic thermo-mechanical behaviour and the changes in the fuel microstructure during deformation. Stoichiometric UO 2 pellets with various grains sizes from 9 pm to 36 μm have been deformed by compression at intermediate temperatures, i.e. near T M /2, and quenched under stress. The damage is characterised by the presence of cavities at low stresses and cracks at high stresses, both along grain boundaries parallel to the compression axis. Inside grains, dislocations organise themselves into cellular substructures in which sub-boundaries are made of dislocation hexagonal networks. In these conditions, uranium dioxide deformation is described by grain boundary sliding, which is the main origin of material damage, partially accommodated by dislocational creep inside grains. A steady-state creep model is proposed on a physical basis. It accounts for the almost similar contributions of two mechanisms which are grain boundaries sliding and intragranular creep, and takes into account the grain boundary roughness. In contrast with phenomenological descriptions used up to now, this picture leads to a unique creep law on the whole range of stresses explored here, from 10 MPa to 80 MPa. The creep rate controlling mechanism seems to be the migration of sub-boundaries. The deformation at constant strain rate is controlled by the same mechanisms as creep. (author) [fr

Fracture toughness and fracture surface energy of sintered uranium dioxide fuel pellets

International Nuclear Information System (INIS)

Kutty, T.R.G.; Chandrasekharan, K.N.; Panakkal, J.P.; Ghosh, J.K.

1987-01-01

The paper concerns the variation of fracture toughness Ksub(ic) and fracture surface energy γsub(s) in sintered uranium dioxide pellets in the density range 9.86 to 10.41 g cm -3 , using Vickers indentation technique. A minimum of four indentations were made on each pellet sample and the average crack length of each indentation and the hardness values were determined. The overall average crack-length datra and the data on volume fraction porosity in the pellets fitted a straight line, from which Ksub(ic) and γsub(s) were calculated. The fracture parameters of nonporous polycrystalline UO 2 , calculated from the experimental data, are presented in tabular form. (U.K.)

Standard test methods for analysis of sintered gadolinium oxide-uranium dioxide pellets

CERN Document Server

American Society for Testing and Materials. Philadelphia

2006-01-01

1.1 These test methods cover procedures for the analysis of sintered gadolinium oxide-uranium dioxide pellets to determine compliance with specifications. 1.2 The analytical procedures appear in the following order: Section Carbon (Total) by Direct CombustionThermal Conductivity Method C1408 Test Method for Carbon (Total) in Uranium Oxide Powders and Pellets By Direct Combustion-Infrared Detection Method Chlorine and Fluorine by Pyrohydrolysis Ion-Selective Electrode Method C1502 Test Method for Determination of Total Chlorine and Fluorine in Uranium Dioxide and Gadolinium Oxide Gadolinia Content by Energy-Dispersive X-Ray Spectrometry C1456 Test Method for Determination of Uranium or Gadolinium, or Both, in Gadolinium Oxide-Uranium Oxide Pellets or by X-Ray Fluorescence (XRF) Hydrogen by Inert Gas Fusion C1457 Test Method for Determination of Total Hydrogen Content of Uranium Oxide Powders and Pellets by Carrier Gas Extraction Isotopic Uranium Composition by Multiple-Filament Surface-Ioni...

On the nature of the phase transition in uranium dioxide

Science.gov (United States)

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

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

Boron-Coated Straw Collar for Uranium Neutron Coincidence Collar Replacement

International Nuclear Information System (INIS)

Hu, Jianwei; Croft, Stephen; McElroy, Robert Dennis

2017-01-01

The objective of this project was to design and optimize, in simulation space, an active neutron coincidence counter (or collar) using boron-coated straws (BCSs) as a non- 3 He replacement to the Uranium Neutron Coincidence Collar (UNCL). UNCL has been used by the International Atomic Energy Agency (IAEA) and European Atomic Energy Community (Euratom) since the 1980s to verify the 235 U content in fresh light water reactor fuel assemblies for safeguards purposes. This report documents the design and optimization of the BCS collar.

Evaluation of uranium dioxide thermal conductivity using molecular dynamics simulations

International Nuclear Information System (INIS)

Kim, Woongkee; Kaviany, Massoud; Shim, J. H.

2014-01-01

It can be extended to larger space, time scale and even real reactor situation with fission product as multi-scale formalism. Uranium dioxide is a fluorite structure with Fm3m space group. Since it is insulator, dominant heat carrier is phonon, rather than electrons. So, using equilibrium molecular dynamics (MD) simulation, we present the appropriate calculation parameters in MD simulation by calculating thermal conductivity and application of it to the thermal conductivity of polycrystal. In this work, we investigate thermal conductivity of uranium dioxide and optimize the parameters related to its process. In this process, called Green Kubo formula, there are two parameters i.e correlation length and sampling interval, which effect on ensemble integration in order to obtain thermal conductivity. Through several comparisons, long correlation length and short sampling interval give better results. Using this strategy, thermal conductivity of poly crystal is obtained and comparison with that of pure crystal is made. Thermal conductivity of poly crystal show lower value that that of pure crystal. In further study, we broaden the study to transport coefficient of radiation damaged structures using molecular dynamics. Although molecular dynamics is tools for treating microscopic scale, most macroscopic issues related to nuclear materials such as voids in fuel materials and weakened mechanical properties by radiation are based on microscopic basis. Thus, research on microscopic scale would be expanded in this field and many hidden mechanism in atomic scales will be revealed via both atomic scale simulations and experiments

Operating conditions of T.B.P. line uranium purification plant, for uranium dioxide production

International Nuclear Information System (INIS)

Vardich, R.N.; La Gamma, A.M.; Anasco, R.; Soler, S.M.G. de; Isnardi, E.; Gea, V.; Chiaraviglio, R.; Matyjasczyk, E.; Aramayo, R.

1992-01-01

In this contribution are presented the operative conditions and the results obtained step of the Uranium dioxide production plant of Argentina. The refining step involve the Uranium concentrate dissolution, the silica ageing, the filtration and liquid - liquid extraction with n-tributyl phosphate solution in kerosene. The established operative conditions allow to obtain Uranyl nitrate solutions of nuclear purity in industrial scale. (author)

URANIUM OXIDE-CONTAINING FUEL ELEMENT COMPOSITION AND METHOD OF MAKING SAME

Science.gov (United States)

Handwerk, J.H.; Noland, R.A.; Walker, D.E.

1957-09-10

In the past, bodies formed of a mixture of uranium dioxide and aluminum powder have been used in fuel elements; however, these mixtures were found not to be suitable when exposed to temperatures of about 600 deg C, because at such high temperatures the fuel elements were distorted. If uranosic oxide, U/sub 3/O/sub 8/, is substituted for UO/sub 2/, the mechanical properties are not impaired when these materials are used at about 600 deg C and no distortion takes place. The uranosic oxide and aluminum, both in powder form, are first mixed, and after a homogeneous mixture has been obtained, are shaped into fuel elements by extrusion at elevated temperature. Magnesium powder may be used in place of the aluminum.

Testing of reactor fuel materials using nuclear techniques

International Nuclear Information System (INIS)

Khouri, M.T.F.C.

1978-01-01

The tests presented here apply to: the quantitative determination of uranium in the core of fuel element plates by the detection of the number of neutrons produced in photo induced reactions in uranium; the determination of 235 U proportion in uranium dioxide samples, in the form of uranyl nitrate, by the technique of the detection of tracks produced by fission fragments and in pellet samples by passive gamma spectrometry and the checking of uranium homogenization distribution in fuel plates and uranium dioxide pellets. (Author) [pt

Nuclear fuel rod with burnable plate and pellet-clad interaction fix

International Nuclear Information System (INIS)

Boyle, R.F.

1987-01-01

This patent describes a nuclear fuel rod comprising a metallic tubular cladding containing nuclear fuel pellets, the pellets containing enriched uranium-235. The improvement described here comprises: ceramic wafers, each wafter comprising a sintered mixture of gadolinium oxide and uranium dioxide, the uranium oxide having no more uranium-235 than is present in natural uranium dioxide. Each of the wafers is axially disposed between a major portion of adjacent the nuclear fuel pellets, whereby the wafers freeze out volatile fission products produced by the nuclear fuel and prevent interaction of the fission products with the metallic tubing cladding

Study of ion plating parameters, coating structure, and corrosion protection for aluminum coatings on uranium

International Nuclear Information System (INIS)

Egert, C.M.; Scott, D.G.

1987-01-01

A study of ion-plating parameters (primarily deposition rate and substrate bias voltage), coating structure, and the corrosion protection provided by aluminum coatings on uranium is presented. Ion plating at low temperatures yields a variety of aluminum coating structures on uranium. For example, aluminum coatings produced at high deposition rates and low substrate bias voltages are columnar with voids between columns, as expected for high-rate vapor deposition at low temperatures. On the other hand, low deposition rate and high bias voltage produce a modified coating with a dense, noncolumnar structure. These results are not in agreement with other studies that have found no relationship between deposition rate and coating structure in ion plating. This discrepancy is probably due to the high deposition rates used in these studies. An accelerated, water vapor corrosion test indicates that the columnar aluminum coatings provide some corrosion protection despite their porous nature; however, the dense noncolumnar coatings provide significantly greater protection. These results indicate that ion-plated aluminum coatings produced at low deposition rates and high substrate bias voltages creates dense coating structures that are most effective in protecting uranium from corrosion

Improved ionic model of liquid uranium dioxide

NARCIS (Netherlands)

Gryaznov, [No Value; Iosilevski, [No Value; Yakub, E; Fortov, [No Value; Hyland, GJ; Ronchi, C

The paper presents a model for liquid uranium dioxide, obtained by improving a simplified ionic model, previously adopted to describe the equation of state of this substance [1]. A "chemical picture" is used for liquid UO2 of stoichiometric and non-stoichiometric composition. Several ionic species

Economic analysis of thorium-uranium fuel cycle introduced into PWRs

International Nuclear Information System (INIS)

Fan Li; Sun Qian

2014-01-01

Using PWR of Daya Bay Unit l as the reference reactor, a validated computer code was used to calculate the fuel cycle costs for uranium fuel cycle and thorium-uranium fuel cycle over the following 20 0perational years respectively. The calculation results show that the thorium-uranium fuel cycle is economically competitive with the uranium fuel cycle when reprocessing mode is adopted. For thorium-uranium fuel cycle, if the price of natural uranium is higher than 120 $ /pound U_3O_8, the fuel cycle cost of the direct disposal mode is greater than that of the reprocessing mode. Therefore, when the uranium price may maintain a high level long-termly, adopting reprocessing mode will benefit the economic advantage for the thorium-uranium fuel cycle introduced into PWRs. (authors)

Nuclear energy - Uranium dioxide pellets - Determination of density and volume fraction of open and closed porosity. 2. ed. 2. ed.

International Nuclear Information System (INIS)

2008-01-01

This International Standard describes a method for determining the chlorine and fluorine concentrations in uranium dioxide and in sintered fuel pellets by pyrohydrolysis of samples, followed either by liquid ion-exchange chromatography or by selective electrode measurement of chlorine and fluorine ions. Many ion-exchange chromatography systems and ion-selective electrode measurement systems are available

Boron-Coated Straw Collar for Uranium Neutron Coincidence Collar Replacement

Energy Technology Data Exchange (ETDEWEB)

Hu, Jianwei [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Croft, Stephen [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); McElroy, Robert Dennis [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

2017-01-01

The objective of this project was to design and optimize, in simulation space, an active neutron coincidence counter (or collar) using boron-coated straws (BCSs) as a non-³He replacement to the Uranium Neutron Coincidence Collar (UNCL). UNCL has been used by the International Atomic Energy Agency (IAEA) and European Atomic Energy Community (Euratom) since the 1980s to verify the ²³⁵U content in fresh light water reactor fuel assemblies for safeguards purposes. This report documents the design and optimization of the BCS collar.

Sintering uranium oxide in the reaction product of hydrogen-carbon dioxide mixtures

International Nuclear Information System (INIS)

De Hollander, W.R.; Nivas, Y.

1975-01-01

Compacted pellets of uranium oxide alone or containing one or more additives such as plutonium dioxide, gadolinium oxide, titanium dioxide, silica, and alumina are heated to 900 to 1599 0 C in the presence of a mixture of hydrogen and carbon dioxide, either alone or with an inert carrier gas and held at the desired temperature in this atmosphere to sinter the pellets. The sintered pellets are then cooled in an atmosphere having an oxygen partial pressure of 10 -4 to 10 -18 atm of oxygen such as dry hydrogen, wet hydrogen, dry carbon monoxide, wet carbon monoxide, inert gases such as nitrogen, argon, helium, and neon and mixtures of ayny of the foregoing including a mixture of hydrogen and carbon dioxide. The ratio of hydrogen to carbon dioxide in the gas mixture fed to the furnace is controlled to give a ratio of oxygen to uranium atoms in the sintered particles within the range of 1.98:1 to about 2.10:1. The water vapor present in the reaction products in the furnace atmosphere acts as a hydrolysis agent to aid removal of fluoride should such impurity be present in the uranium oxide. (U.S.)

Study of Physical modifications induced by chromium doping of uranium dioxide

International Nuclear Information System (INIS)

Fraczkiewicz, M.

2010-01-01

Improvement of nuclear fuel performances requires reducing fission gas release. Doping uranium dioxide with chromium is the improvement axis considered in this work. Indeed, chromium fastens crystal growth in UO 2 , and thus enables a significant increase of the grain size. This work aims at the identification of defects produced by chromium addition in UO 2 , and their impact on properties of interest of the material. First, defects existing in doped fuel directly after sintering have been studied. X-ray Absorption Spectroscopy allowed the identification of the environment of solubilised chromium in UO 2 . Chromium atoms are roughly substituting for uranium atoms, but generate a complete reorganisation of neighbouring oxygen atoms, and distortion of uranium sublattice. Characterisation of transport properties (electrical conductivity and oxygen self-diffusion) have shown that because of charge balance, chromium plays a leading role on such properties. A model of point defects in UO 2 has been proposed, showing how complex the involved phenomena are. Observations by Transmission Electron Microscopy of ion-irradiated thin foils have shown that chromium makes the coalescence of irradiation defects easier. This behaviour can be explained by a stabilisation of defect clusters due to precipitation of chromium. Finally, study of thermal diffusion of helium in doped UO 2 , performed by Nuclear Reaction Analysis, has confirmed this interaction between chromium atoms and irradiation defects. Indeed, μ-NRA measures have shown no fast gas diffusion close to grain boundaries, in contrast with standard UO 2 behaviour, which is associated with defects recovery in grain boundaries. (author) [fr

NEUTRONICS STUDIES OF URANIUM-BASED FULLY CERAMIC MICRO-ENCAPSULATED FUEL FOR PWRs

Energy Technology Data Exchange (ETDEWEB)

George, Nathan M [ORNL; Maldonado, G Ivan [ORNL; Terrani, Kurt A [ORNL; Gehin, Jess C [ORNL; Godfrey, Andrew T [ORNL

2012-01-01

This study evaluates the core neutronics and fuel cycle characteristics that result from employing uranium-based fully ceramic micro-encapsulated (FCM) fuel in a pressurized water reactor (PWR). Specific PWR bundle designs with FCM fuel have been developed, which by virtue of their TRISO particle based elements, are expected to safely reach higher fuel burnups while also increasing the tolerance to fuel failures. The SCALE 6.1 code package, developed and maintained at ORNL, was the primary software employed to model these designs. Analysis was performed using the SCALE double-heterogeneous (DH) fuel modeling capabilities. For cases evaluated with the NESTLE full-core three-dimensional nodal simulator, because the feature to perform DH lattice physics branches with the SCALE/TRITON sequence is not yet available, the Reactivity-Equivalent Physical Transformation (RPT) method was used as workaround to support the full core analyses. As part of the fuel assembly design evaluations, fresh feed lattices were modeled to analyze the within-assembly pin power peaking. Also, a color-set array of assemblies was constructed to evaluate power peaking and power sharing between a once-burned and a fresh feed assembly. In addition, a parametric study was performed by varying the various TRISO particle design features; such as kernel diameter, coating layer thicknesses, and packing fractions. Also, other features such as the selection of matrix material (SiC, Zirconium) and fuel rod dimensions were perturbed. After evaluating different uranium-based fuels, the higher physical density of uranium mononitride (UN) proved to be favorable, as the parametric studies showed that the FCM particle fuel design will need roughly 12% additional fissile material in comparison to that of a standard UO2 rod in order to match the lifetime of an 18-month PWR cycle. Neutronically, the FCM fuel designs evaluated maintain acceptable design features in the areas of fuel lifetime, temperature

Certification of a uranium dioxide reference material for chemical analyses

International Nuclear Information System (INIS)

Le Duigou, Y.

1984-01-01

This report, issued by the Central Bureau for Nuclear Measurements (CBNM), describes the characterization of a uranium dioxide reference material with accurately determined uranium mass fraction for chemical analyses. The preparation, conditioning, homogeneity tests and the analyses performed on this material are described in Annex 1. The evaluation of the individual impurity results, total of impurities and uranium mass fraction are given in Annex 2. Information on a direct determination of uranium by titration is given in Annex 3. The uranium mass fraction (881.34+-0.13) g.kg -1 calculated in Annex 2 is given on the certificate

Determination of gas residues in uranium dioxide pellets

International Nuclear Information System (INIS)

Riella, H.G.

1978-01-01

The measurement of low amounts of residual gases, excluding water, in ceramic grade uranium dioxide pellets, using high temperature vacuum extraction technique, is dealt with. The high temperature extraction gas analysis apparatus was designed and assembled for sequential analysis of up to eight uranium dioxide pellets by run. The system consists of three major units, namely outgassing unit, transfer unit and analytical unit. The whole system is evacuated to a final pressure of less then 10 -5 torr. A weighed pellet is transfered into the outgassing unit for subsequent dropping into a Platinum-Rhodium crucible which is heated inductively up to 1600 0 C during 30 minutes. The released gases are imediately transfered from the outgassing to analytical unit passing through a cold trap at -95 0 C to remove water vapor. The gases are transfered to previously calibrated volumetric bulb where the total pressure and temperature are determined. An estimate of the gas content in the pellets at STP condition is obtained from the measured volume, pressure and temperature of the gas mixture by applying ideal gases equation. Analysis to two lots (fourteen samples) of uranium dioxide pellets by the method described here indicated a mean gas content of 0,060cm 3 /g UO 2 . The lower limit of this technique is 0,03cm 3 /g UO 2 (STP). The time required for the analysis of eight pellets is about 9 hours [pt

Results of Uranium Dioxide-Tungsten Irradiation Test and Post-Test Examination

Science.gov (United States)

Collins, J. F.; Debogdan, C. E.; Diianni, D. C.

1973-01-01

A uranium dioxide (UO2) fueled capsule was fabricated and irradiated in the NASA Plum Brook Reactor Facility. The capsule consisted of two bulk UO2 specimens clad with chemically vapor deposited tungsten (CVD W) 0.762 and 0.1016 cm (0.030-and 0.040-in.) thick, respectively. The second specimen with 0.1016-cm (0.040-in.) thick cladding was irradiated at temperature for 2607 hours, corresponding to an average burnup of 1.516 x 10 to the 20th power fissions/cu cm. Postirradiation examination showed distortion in the bottom end cap, failure of the weld joint, and fracture of the central vent tube. Diametral growth was 1.3 percent. No evidence of gross interaction between CVD tungsten or arc-cast tungsten cladding and the UO2 fuel was observed. Some of the fission gases passed from the fuel cavity to the gas surrounding the fuel specimen via the vent tube and possibly the end-cap weld failure. Whether the UO2 loss rates through the vent tube were within acceptable limits could not be determined in view of the end-cap weld failure.

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

International Nuclear Information System (INIS)

Silva Neto, Joao Batista da

2008-01-01

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

Standard test methods for chemical, mass spectrometric, and spectrochemical analysis of nuclear-grade uranium dioxide powders and pellets

CERN Document Server

American Society for Testing and Materials. Philadelphia

1999-01-01

1.1 These test methods cover procedures for the chemical, mass spectrometric, and spectrochemical analysis of nuclear-grade uranium dioxide powders and pellets to determine compliance with specifications. 1.2 This test method covers the determination of uranium and the oxygen to uranium atomic ratio in nuclear-grade uranium dioxide powder and pellets. 1.4 This test method covers the determination of chlorine and fluorine in nuclear-grade uranium dioxide. With a 1 to 10-g sample, concentrations of 5 to 200 g/g of chlorine and 1 to 200 μg/g of fluorine are determined without interference. 1.5 This test method covers the determination of moisture in uranium dioxide samples. Detection limits are as low as 10 μg. 1.6 This test method covers the determination of nitride nitrogen in uranium dioxide in the range from 10 to 250 μg. 1.7 This test method covers the spectrographic analysis of nuclear-grade UO2 for the 26 elements in the ranges indicated in Table 2. 1.8 For simultaneous determination of trace ele...

The nuclear fuel cycle: (2) fuel element manufacture

International Nuclear Information System (INIS)

Doran, J.

1976-01-01

Large-scale production of nuclear fuel in the United Kingdom is carried out at Springfields Works of British Nuclear Fuels Ltd., a company formed from the United Kingdom Atomic Energy Authority in 1971. The paper describes in some detail the Springfields Works processes for the conversion of uranium ore concentrate to uranium tetrafluoride, then conversion of the tetrafluoride to either uranium metal for cladding in Magnox to form fuel for the British Mk I gas-cooled reactors, or to uranium hexafluoride for enrichment of the fissile 235 U isotope content at the Capenhurst Works of BNFL. Details are given of the reconversion at Springfields Works of this enriched uranium hexafluoride to uranium dioxide, which is pelleted and then clad in either stainless steel or zircaloy containers to form the fuel assemblies for the British Mk II AGR or advanced gas-cooled reactors or for the water reactor fuels. (author)

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

Development of the uranium recovery process from rejected fuel plates in the fabrication of MTR type nuclear fuel

International Nuclear Information System (INIS)

Fleming Rubio, Peter Alex

2010-01-01

The current work was made in Conversion laboratory belonging to Chilean Nuclear Energy Commission, CCHEN. This is constituted by the development of three hydrometallurgical processes, belonging to the recovery of uranium from fuel plates based on uranium silicide (U_3Si_2) process, for nuclear research reactors MTR (Material Testing Reactor) type, those that come from the Fuel Elements Manufacture Plant, PEC. In the manufacturing process some of these plates are subjected to destructive tests by quality requirement or others are rejected for non-compliance with technical specifications, such as: lack of homogenization of the dispersion of uraniferous compound in the meat, as well as the appearance of the defects, such as blisters, so-called "dog bone", "fish tail", "remote islands", among others. Because the uranium used is enriched in 19.75% U_2_3_5 isotope, which explains the high value in the market, it must be recovered for reuse, returning to the production line of fuel elements. The uranium silicide, contained in the plates, is dispersed in an aluminum matrix and covered with plates and frames of ASTM 6061 Aluminum, as a sandwich coating, commonly referred to as 'meat' (sandwich meat). As aluminum is the main impurity, the process begins with this metal dissolution, present in meat and plates, by NaOH reaction, followed by a vacuum filtration, washing and drying, obtaining a powder of uranium silicide, with a small impurities percentage. Then, the crude uranium silicide reacts with a solution of hydrofluoric acid, dissolving the silicon and simultaneously precipitating UF_4 by reaction with HNO_3, obtaining an impure UO_2(NO_3)_2 solution. The experimental work was developed and implemented at laboratory scale for the three stages pertaining to the uranium recovery process, determining for each one the optimum operation conditions: temperature, molarity or concentration, reagent excess, among others (author)

Phenomena in thermal transport in fuels

International Nuclear Information System (INIS)

Chernatynskiy, A.; Tulenko, J.S.; Phillpot, S.R.; El-Azab, A.

2015-01-01

Thermal transport in nuclear fuels is a key performance metric that affects not only the power output, but is also an important consideration in potential accident situations. While the fundamental theory of the thermal transport in crystalline solids was extensively developed in the 1950's and 1960's, the pertinent analytic approaches contained significant simplifications of the physical processes. While these approaches enabled estimates of the thermal conductivity in bulk materials with microstructure, they were not comprehensive enough to provide the detailed guidance needed for the in-pile fuel performance. Rather, this guidance has come from data painfully accumulated over 50 years of experiments on irradiated uranium dioxide, the most widely used nuclear fuel. At this point, a fundamental theoretical understanding of the interplay between the microstructure and thermal conductivity of irradiated uranium dioxide fuel is still lacking. In this chapter, recent advances are summarised in the modelling approaches for thermal transport of uranium dioxide fuel. Being computational in nature, these modelling approaches can, at least in principle, describe in detail virtually all mechanisms affecting thermal transport at the atomistic level, while permitting the coupling of the atomistic-level simulations to the mesoscale continuum theory and thus enable the capture of the impact of microstructural evolution in fuel on thermal transport. While the subject of current studies is uranium dioxide, potential applications of the methods described in this chapter extend to the thermal performance of other fuel forms. (authors)

Theoretical study using electronic structure calculations of uranium and cerium dioxides containing defects and impurities

International Nuclear Information System (INIS)

Shi, Lei

2016-01-01

Uranium dioxide (UO_2) is the most widely used nuclear fuel in existing nuclear reactors around the world. While in service for energy supply, UO_2 is submitted to the neutron flux and undergoes nuclear fission chain reactions, which create large number of fission products and point defects. The study of the behavior of the fission products and point defects is important to understand the fuel properties under irradiation. We conduct electronic structure calculations based on the density functional theory (DFT) to model this radiation damage at the atomic scale. The DFT+U method is used to describe the strong correlation of the 4f electrons of cerium and 5f electrons of uranium in the materials studied (UO_2, CeO_2 and (U, Ce)O_2). (U, Ce)O_2 is studied because it is considered as a low radioactive model material of mixed actinide oxides such as the MOX fuel (U, Pu)O_2 used in light water reactors and fast neutron reactors. Cerium dioxide (CeO_2) is studied to provide reference data of (U, Ce)O_2. We perform a DFT+U study of point defects and gaseous fission products (Xe and Kr) in CeO_2 and compare our results to the existing ones of UO_2. We study the bulk properties as well as the behavior of defects for (U, Ce)O_2, and compare our results to the ones of (U, Pu)O_2. Furthermore, for the study of defects in UO_2, methodological improvements are explored considering the spin-orbit coupling effect and the finite-size effect of the simulation supercell. (author) [fr

Impact of fuel fabrication and fuel management technologies on uranium management

International Nuclear Information System (INIS)

Arnsberger, P.L.; Stucker, D.L.

1994-01-01

Uranium utilization in commercial pressurized water reactors is a complex function of original NSSS design, utility energy requirements, fuel assembly design, fuel fabrication materials and fuel fabrication materials and fuel management optimization. Fuel design and fabrication technologies have reacted to the resulting market forcing functions with a combination of design and material changes. The technologies employed have included ever-increasing fuel discharge burnup, non-parasitic structural materials, burnable absorbers, and fissile material core zoning schemes (both in the axial and radial direction). The result of these technological advances has improved uranium utilization by roughly sixty percent from the infancy days of nuclear power to present fuel management. Fuel management optimization technologies have also been developed in recent years which provide fuel utilization improvements due to core loading pattern optimization. This paper describes the development and impact of technology advances upon uranium utilization in modern pressurized water reactors. 10 refs., 3 tabs., 10 figs

Method for providing uranium with a protective copper coating

Science.gov (United States)

Waldrop, Forrest B.; Jones, Edward

1981-01-01

The present invention is directed to a method for providing uranium metal with a protective coating of copper. Uranium metal is subjected to a conventional cleaning operation wherein oxides and other surface contaminants are removed, followed by etching and pickling operations. The copper coating is provided by first electrodepositing a thin and relatively porous flash layer of copper on the uranium in a copper cyanide bath. The resulting copper-layered article is then heated in an air or inert atmosphere to volatilize and drive off the volatile material underlying the copper flash layer. After the heating step an adherent and essentially non-porous layer of copper is electro-deposited on the flash layer of copper to provide an adherent, multi-layer copper coating which is essentially impervious to corrosion by most gases.

Slightly enriched uranium fuel for a PHWR

International Nuclear Information System (INIS)

Notari, C.; Marajofsky, A.

1997-01-01

An improved fuel element design for a PHWR using slightly enriched uranium fuel is presented. It maintains the general geometric disposition of the currently used in the argentine NPP's reactors, replacing the outer ring of rods by rods containing annular pellets. Power density reduction is achieved with modest burnup losses and the void volume in the pellets can be used to balance these two opposite effects. The results show that with this new design, the fuel can be operated at higher powers without violating thermohydraulic limits and this means an improvement in fuel management flexibility, particularly in the transition from natural uranium to slightly enriched uranium cycle. (author)

The uranium-plutonium breeder reactor fuel cycle

International Nuclear Information System (INIS)

Salmon, A.; Allardice, R.H.

1979-01-01

All power-producing systems have an associated fuel cycle covering the history of the fuel from its source to its eventual sink. Most, if not all, of the processes of extraction, preparation, generation, reprocessing, waste treatment and transportation are involved. With thermal nuclear reactors more than one fuel cycle is possible, however it is probable that the uranium-plutonium fuel cycle will become predominant; in this cycle the fuel is mined, usually enriched, fabricated, used and then reprocessed. The useful components of the fuel, the uranium and the plutonium, are then available for further use, the waste products are treated and disposed of safely. This particular thermal reactor fuel cycle is essential if the fast breeder reactor (FBR) using plutonium as its major fuel is to be used in a power-producing system, because it provides the necessary initial plutonium to get the system started. In this paper the authors only consider the FBR using plutonium as its major fuel, at present it is the type envisaged in all, current national plans for FBR power systems. The corresponding fuel cycle, the uranium-plutonium breeder reactor fuel cycle, is basically the same as the thermal reactor fuel cycle - the fuel is used and then reprocessed to separate the useful components from the waste products, the useful uranium and plutonium are used again and the waste disposed of safely. However the details of the cycle are significantly different from those of the thermal reactor cycle. (Auth.)

Fuel particle coating data

International Nuclear Information System (INIS)

Hollabaugh, C.M.; Wagner, P.; Wahman, L.A.; White, R.W.

1977-01-01

Development of coating on nuclear fuel particles for the High-Temperature Fuels Technology program at the Los Alamos Scientific Laboratory included process studies for low-density porous and high-density isotropic carbon coats, and for ZrC and ''alloy'' C/ZrC coats. This report documents the data generated by these studies

Measurement of enriched uranium and uranium-aluminum fuel materials with the AWCC

International Nuclear Information System (INIS)

Krick, M.S.; Menlove, H.O.; Zick, J.; Ikonomou, P.

1985-05-01

The active well coincidence counter (AWCC) was calibrated at the Chalk River Nuclear Laboratories (CRNL) for the assay of 93%-enriched fuel materials in three categories: (1) uranium-aluminum billets, (2) uranium-aluminum fuel elements, and (3) uranium metal pieces. The AWCC was a standard instrument supplied to the International Atomic Energy Agency under the International Safeguards Project Office Task A.51. Excellent agreement was obtained between the CRNL measurements and previous Los Alamos National Laboratory measurements on similar mockup fuel material. Calibration curves were obtained for each sample category. 2 refs., 8 figs., 15 tabs

Nuclear fuel, with emphasis on its utilization in pressurized water reactor

International Nuclear Information System (INIS)

Khazaneh, R.; Roshanzamir, M.

1997-01-01

Production processes of nuclear fuel on one hand and using nuclear fuels in reactors, particularly PWR Type reactors on the other hand is investigated. The first chapter reviews the relationship between fuel and reactors; The principals of reactor physics in relation with fuel are described shortly. The second chapter reviews uranium exploration and extraction as well as production of uranium concentrate and uranium dioxides. The third chapter is specified to the different procedures of uranium enrichment. In the fourth chapter, processing of uranium dioxide powder and fuel pellet is described. In the fifth chapter fabrication of fuel rod and fuel assemblies is explained thoroughly. The sixth chapter devoted to the different phenomena which occur ed in fuel structure and can during operational time of reactor; damage to fuel rods and developing theoretical models to describe these phenomena and analysis of fuel structure. The seventh chapter discusses how fuel rods are to be experimented during fabrication, operation and development of technology. The eighth chapter explains different fuels such as uranium compounds and mixed oxide fuel of uranium Gadolinium and uranium plutonium and the process of fabrication of zircaloy. In the tenth chapter, fuel reprocessing is investigated and the difficulties of developing this technology is referred

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

International Nuclear Information System (INIS)

Mac Donald, Philip Elsworth

2002-01-01

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

Potential health hazard of nuclear fuel waste and uranium ore

International Nuclear Information System (INIS)

Mehta, K.; Sherman, G.R.; King, S.G.

1991-06-01

The variation of the radioactivity of nuclear fuel waste (used fuel and fuel reprocessing waste) with time, and the potential health hazard (or inherent radiotoxicity) resulting from its ingestion are estimated for CANDU (Canada Deuterium Uranium) natural-uranium reactors. Four groups of radionuclides in the nuclear fuel waste are considered: actinides, fission products, activation products of zircaloy, and activation products of fuel impurities. Contributions from each of these groups to the radioactivity and to the potential health hazard are compared and discussed. The potential health hazard resulting from used fuel is then compared with that of uranium ore, mine tailings and refined uranium (fresh fuel) on the basis of equivalent amounts of uranium. The computer code HAZARD, specifically developed for these computations, is described

Monte Carlo criticality analysis of simple geometries containing tungsten-rhenium alloys engrained with uranium dioxide and uranium mononitride

International Nuclear Information System (INIS)

Webb, Jonathan A.; Charit, Indrajit

2011-01-01

Highlights: → The addition of rhenium to the tungsten matrix within W-UO 2 and W-UN CERMET materials can help reduce the risk of submersion criticality accidents while increasing the strength and ductility of tungsten based nuclear fuel elements. → The addition of rhenium up to 30 at.% to simple geometries containing W-UO 2 mixtures can increase the critical mass by 65 kg. → The addition of rhenium up to 30 at.% to simple geometries containing W-UN mixtures can increase the critical mass by 22 kg. → The addition of rhenium by up to 30 at.% to simple geometries containing W-UO 2 mixtures can reduce the change in reactivity change due to water submersion by $5.07. → The addition of rhenium by up to 30 at.% to simple geometries containing W-UN mixtures can reduce the change in reactivity due to water submersion by $3.24. - Abstract: The critical mass and dimensions of simple geometries containing highly enriched uranium dioxide (UO 2 ) and uranium mononitride (UN) encapsulated in tungsten-rhenium alloys are determined using MCNP5 criticality calculations. Spheres as well as cylinders with length to radius ratios of 1.82 are computationally built to consist of 60 vol.% fuel and 40 vol.% metal matrix. Within the geometries, the uranium is enriched to 93 wt.% uranium-235 and the rhenium content within the metal alloy was modeled over the range of 0-30 at.%. The spheres containing UO 2 were determined to have a critical radius of 18.29-19.11 cm and a critical mass ranging from 366 kg to 424 kg. The cylinders containing UO 2 were found to have a critical radius ranging from 17.07 cm to 17.84 cm with a corresponding critical mass of 406-471 kg. Spheres engrained with UN were determined to have a critical radius ranging from 14.82 cm to 15.19 cm and a critical mass between 222 kg and 242 kg. Cylinders which were engrained with UN were determined to have a critical radius ranging from 13.81 cm to 14.15 cm and a corresponding critical mass of 245-267 kg. The critical

Dissolution testing of intermediary products in uranium dioxide production by the sol-gel method

International Nuclear Information System (INIS)

Melichar, F.; Landspersky, H.; Urbanek, V.

1979-01-01

A method was developed of dissolving polyuranates and uranium dioxides in sulphuric acid and in carbonate solutions for testing intermediate products in the sol-gel process preparation of uranium dioxide. A detailed granulometric analysis of spherical particle dispersion was included as part of the tests. Two different production methods were used for the two types of studied materials. The test results show that the test method is suitable for determining temperature sensitivity of the materials to dissolution reaction. The geometrical distribution of impurities in the spherical particles can be determined from the dissolution kinetics. The method allows the determination of the effect of carbon from impurities on the process of uranium dioxide leaching and is thus applicable for testing materials prepared by the sol-gel method. (Z.M.)

Plasma sprayed and electrospark deposited zirconium metal diffusion barrier coatings

International Nuclear Information System (INIS)

Hollis, Kendall J.; Pena, Maria I.

2010-01-01

Zirconium metal coatings applied by plasma spraying and electrospark deposition (ESD) have been investigated for use as diffusion barrier coatings on low enrichment uranium fuel for research nuclear reactors. The coatings have been applied to both stainless steel as a surrogate and to simulated nuclear fuel uranium-molybdenum alloy substrates. Deposition parameter development accompanied by coating characterization has been performed. The structure of the plasma sprayed coating was shown to vary with transferred arc current during deposition. The structure of ESD coatings was shown to vary with the capacitance of the deposition equipment.

Study of uranium dioxide pellets by micro-acoustic techniques

International Nuclear Information System (INIS)

Roque, V.

1999-01-01

In order to reduce the volume of spent fuel to reprocess and to improve the productivity and the safety of the nuclear reactor, 'Electricite De France' aim to increase the average fuel discharge burn-up. To elaborate the safety reports, EDF develops codes to simulate the thermo-mechanical behaviour of the nuclear fuel element. These numeric simulations need to evaluate accurately and locally the evolution of the material and of its properties. One of the major concern today is the local characterisation of the intrinsic volume fraction porosity and the mechanical properties of the irradiated fuel. The fuel pellet fragmentation, the steep radial gradient in its physical properties evolution and the chemical evolution of the irradiated material make difficult nay the use of the conventional techniques. This leads EDF to pay interest for the use of two complementary techniques: micro-indentation on the one hand and acoustic methods on the other hand (acoustic microscopy and micro-echography), with an additional constrain to perform on active materials. The objective of this work has been to adapt the acoustic methods for an application on uranium dioxide pellets, used as nuclear fuel in Water Pressurised Reactor. Acquisitions protocols have been set to measure accurately the Rayleigh velocity and the longitudinal velocity of the UO 2 . Using these protocols, we have calibrated these acoustic methods by analysing non irradiated nuclear pellet which properties were well known. This process enable to quantify the effects of different physico-chemical parameters of the UO 2 on the ultrasonic velocities measured. Particularly, the large influence of the porosity has been demonstrated and empirical laws to express the evolution of the acoustic velocities as a function of the volume fraction porosity were established. Moreover, we have established a methodology to characterise the intrinsic elastic constants and the volume fraction porosity on irradiated UO 2 fuel pellets

Use of depleted uranium silicate glass to minimize release of radionuclides from spent nuclear fuel waste packages

International Nuclear Information System (INIS)

Forsberg, C.W.

1996-01-01

A Depleted Uranium Silicate Container Backfill System (DUSCOBS) is proposed that would use small, isotopically-depleted uranium silicate glass beads as a backfill material inside repository waste packages containing spent nuclear fuel (SNF). The uranium silicate glass beads would fill the void space inside the package including the coolant channels inside SNF assemblies. Based on preliminary analysis, the following benefits have been identified. DUSCOBS improves repository waste package performance by three mechanisms. First, it reduces the radionuclide releases from SNF when water enters the waste package by creating a local uranium silicate saturated groundwater environment that suppresses (a) the dissolution and/or transformation of uranium dioxide fuel pellets and, hence, (b) the release of radionuclides incorporated into the SNF pellets. Second, the potential for long-term nuclear criticality is reduced by isotopic exchange of enriched uranium in SNF with the depleted uranium (DU) in the glass. Third, the backfill reduces radiation interactions between SNF and the local environment (package and local geology) and thus reduces generation of hydrogen, acids, and other chemicals that degrade the waste package system. Finally, DUSCOBS provides a potential method to dispose of significant quantities of excess DU from uranium enrichment plants at potential economic savings. DUSCOBS is a new concept. Consequently, the concept has not been optimized or demonstrated in laboratory experiments

Determining the minimum required uranium carbide content for HTGR UCO fuel kernels

International Nuclear Information System (INIS)

McMurray, Jacob W.; Lindemer, Terrence B.; Brown, Nicholas R.; Reif, Tyler J.; Morris, Robert N.; Hunn, John D.

2017-01-01

Highlights: • The minimum required uranium carbide content for HTGR UCO fuel kernels is calculated. • More nuclear and chemical factors have been included for more useful predictions. • The effect of transmutation products, like Pu and Np, on the oxygen distribution is included for the first time. - Abstract: Three important failure mechanisms that must be controlled in high-temperature gas-cooled reactor (HTGR) fuel for certain higher burnup applications are SiC layer rupture, SiC corrosion by CO, and coating compromise from kernel migration. All are related to high CO pressures stemming from O release when uranium present as UO 2 fissions and the O is not subsequently bound by other elements. In the HTGR kernel design, CO buildup from excess O is controlled by the inclusion of additional uranium apart from UO 2 in the form of a carbide, UC x and this fuel form is designated UCO. Here general oxygen balance formulas were developed for calculating the minimum UC x content to ensure negligible CO formation for 15.5% enriched UCO taken to 16.1% actinide burnup. Required input data were obtained from CALPHAD (CALculation of PHAse Diagrams) chemical thermodynamic models and the Serpent 2 reactor physics and depletion analysis tool. The results are intended to be more accurate than previous estimates by including more nuclear and chemical factors, in particular the effect of transmuted Pu and Np oxides on the oxygen distribution as the fuel kernel composition evolves with burnup.

Separation and mass spectrometry of nanogram quantities of uranium and thorium from thorium-uranium dioxide fuels

International Nuclear Information System (INIS)

Green, L.W.; Elliot, N.L.; Longhurst, T.H.

1983-01-01

A microchemical procedure was developed for the separation and isotopic analysis of U and Th from irradiated (Th,U)O 2 fuel. The separation procedure consisted of two stages; in the first a tributyl phosphate impregnated resin bead was equilibrated with the dissolved fuel in 0.08 M HF/6 M HNO 3 solution. The bead sorbed approximately 1.7 μg of U and 4.8μg of Th and provided good separation of these from the fission products. In the second stage, the U and Th were back-extracted into 0.025 M HF/8 M HNO 3 solution, which contained a small anion-exchange membrane disk. The disk adsorbed approximately 14 ng of U and 45 ng of Th, and subsequently was transferred to the ionizing filament of a thermal-ionization mass spectrometer and covered with a starch deposit. Sensitivities were sufficiently high for sequential analysis of these quantities of Th and U from a single disk. Isotopic data obtained for a combined U and Th standard showed excellent agreement with certified values: overall bias and precision were < 0.03% and 0.2% relative standard deviation, respectively, for both elements. The applicability of the procedure to uranium fuels was also demonstrated. 6 figures, 2 tables

Separation and mass spectrometry of nanogram quantities of uranium and thorium from thorium-uranium dioxide fuels

Energy Technology Data Exchange (ETDEWEB)

Green, L.W.; Elliot, N.L.; Longhurst, T.H

1983-07-01

A convenient and sensitive microchemical procedure was developed for the separation and isotopic analysis of U and Th from irradiated (Th,U)O{sub 2} fuel. The separation procedure consisted of two stages; in the first a tributyl phosphate impregnated resin bead was equilibrated with the dissolved fuel in 0.08 M HF/6 M HNO{sub 3} solution. The bead sorbed approximately 1.7 {mu}g of U and 4.8 {mu}g of Th and provided good separation of these from the fission products. In the second stage, the U and Th were back-extracted into 0.025 M HF/8 M HNO{sub 3} solution, which contained a small anion-exchange membrane disk. The disk adsorbed approximately 14 ng of U and 45 ng of Th, and subsequently was transferred to the ionizing filament of a thermal-ionization mass spectrometer and covered with a starch deposit. Sensitivities were sufficiently high for sequential analysis of these quantities of Th and U from a single disk. Isotopic data obtained for a combined U and Th standard showed excellent agreement with certified values: overall bias and precision were < -0.03% and 0.2% relative standard deviation, respectively, for both elements. The applicability of the procedure to uranium fuels was also demonstrated. (author)

Determination of Oxygen - to - Uranium Ratio in Hyperstoichio - Metric Uranium Dioxide. RCN Report

International Nuclear Information System (INIS)

Tolk, A.; Lingerak, W.A.

1970-09-01

For the determination of the O/U ratio in hyperstoichiometric uranium dioxide we prefer the following chemical procedure. The sample is dissolved in concentrated phosphoric acid without change in valence of the uranium. Then the amount of U (VI) present in the solution is titrated with a Fe (II) - standard solution in phosphoric acid. The titrimetric end-point is detected following the ''dead-stop-end-point'' procedure. When special precautions are made the O/U value can be determined with an accuracy and precision of + 0.0001 0/U units when 500 mg sample aliquots are used. (author)

Surface characterization of uranium metal and uranium dioxide using X-ray photoelectron spectroscopy

International Nuclear Information System (INIS)

Allen, G.C.; Trickle, I.R.; Tucker, P.M.

1981-01-01

X-ray photoelectron spectra of pure uranium metal and stoichiometric uranium dioxide have been obtained using an AEI ES300 spectrometer. Binding energy values for core and valence electrons have been determined using an internally calibrated energy scale and monochromatic Al Kα radiation. Satellite peaks observed accompanying certain principal core ionizations are discussed in relation to the mechanisms by which they arise. Confirmation is obtained that for stoichiometric UOsub(2.00) a single shake-up satellite is observed accompanying the U 4fsub(7/2,5/2) principal core lines, separated by 6.8 eV to higher binding energy. (author)

Predictor of regulation of uranium dioxide powder pressing process

International Nuclear Information System (INIS)

Motta, Eduardo Souza; Araujo, Victor Hugo Leal de; Bernardelli, Sergio Henrique

2007-01-01

One of the most important steps of the uranium dioxide pellets fabrication used in the nuclear fuel elements is the green pellets pressing. The target density of the pellets after the sintering process determines the density of the green pellet. To meet the same sintered target density the green density may vary according to the powder characteristics. These variations implies in changing the regulation of the press for different powder's patches. The regulation done empirically imply in productivity loss and necessity of reprocessing the pellets pressed during the press regulation and also depends on the operator experience. At this work, was developed an artificial neural network feed forward back propagation to predict the press regulation, depending on the powder characteristics and the green pellet's target density. The results obtained at INB - Industrias Nucleares do Brasil S. A. during the fabrication of the fifth recharge of Angra II nuclear power plant are presented. (author)

Fuel powder production from ductile uranium alloys

International Nuclear Information System (INIS)

Clark, C.R.; Meyer, M.K.

1998-01-01

Metallic uranium alloys are candidate materials for use as the fuel phase in very-high-density LEU dispersion fuels. These ductile alloys cannot be converted to powder form by the processes routinely used for oxides or intermetallics. Three methods of powder production from uranium alloys have been investigated within the US-RERTR program. These processes are grinding, cryogenic milling, and hydride-dehydride. In addition, a gas atomization process was investigated using gold as a surrogate for uranium. (author)

Estimation of irradiation-induced material damage measure of FCM fuel in LWR core

International Nuclear Information System (INIS)

Lee, Kyung-Hoon; Lee, Chungchan; Park, Sang-Yoon; Cho, Jin-Young; Chang, Jonghwa; Lee, Won Jae

2014-01-01

An irradiation-induced material damage measure on tri-isotropic (TRISO) multi-coating layers of fully ceramic micro-encapsulated (FCM) fuel to replace conventional uranium dioxide (UO 2 ) fuel for existing light water reactors (LWRs) has been estimated using a displacement per atom (DPA) cross section for a FCM fuel performance analysis. The DPA cross sections in 47 and 190 energy groups for both silicon carbide (SiC) and graphite are generated based on the molecular dynamics simulation by SRIM/TRIM. For the selected FCM fuel assembly design with FeCrAl cladding, a core depletion analysis was carried out using the DeCART2D/MASTER code system with the prepared DPA cross sections to evaluate the irradiation effect in the Korean OPR-1000. The DPA of the SiC and IPyC coating layers is estimated by comparing the discharge burnup obtained from the MASTER calculation with the burnup-dependent DPA for each coating layer calculated using DeCART2D. The results show that low uranium loading and hardened neutron spectrum compared to that of high temperature gas-cooled reactor (HTGR) result in high discharge burnup and high fast neutron fluence. In conclusion, it can be seen that the irradiation-induced material damage measure is noticeably increased under LWR operating conditions compared to HTGRs. (author)

Neutronics Studies Of Uranium-Based Fully Ceramic Micro-Encapsulated Fuel For PWRs

International Nuclear Information System (INIS)

Maldonado, G. Ivan; Gehin, Jess C.

2012-01-01

This study evaluates the core neutronics and fuel cycle characteristics that result from employing uranium-based fully ceramic micro-encapsulated (FCM) fuel in a pressurized water reactor (PWR). Specific PWR bundle designs with FCM fuel have been developed, which by virtue of their TRISO particle based elements, are expected to safely reach higher fuel burnups while also increasing the tolerance to fuel failures. The SCALE 6.1 code package, developed and maintained at ORNL, was the primary software employed to model these designs. Analysis was performed using the SCALE double-heterogeneous (DH) fuel modeling capabilities. For cases evaluated with the NESTLE full-core three-dimensional nodal simulator, because the feature to perform DH lattice physics branches with the SCALE/TRITON sequence is not yet available, the Reactivity-Equivalent Physical Transformation (RPT) method was used as workaround to support the full core analyses. As part of the fuel assembly design evaluations, fresh feed lattices were modeled to analyze the within-assembly pin power peaking. Also, a color-set array of assemblies was constructed to evaluate power peaking and power sharing between a once-burned and a fresh feed assembly. In addition, a parametric study was performed by varying the various TRISO particle design features; such as kernel diameter, coating layer thicknesses, and packing fractions. Also, other features such as the selection of matrix material (SiC, Zirconium) and fuel rod dimensions were perturbed. After evaluating different uranium-based fuels, the higher physical density of uranium mononitride (UN) proved to be favorable, as the parametric studies showed that the FCM particle fuel design will need roughly 12% additional fissile material in comparison to that of a standard UO2 rod in order to match the lifetime of an 18-month PWR cycle. Neutronically, the FCM fuel designs evaluated maintain acceptable design features in the areas of fuel lifetime, temperature

Uranium dioxide Caramel fuel

International Nuclear Information System (INIS)

Schwartz, J.P.

The work performed in France on Caramel fuels for research reactors reflects the reality of a program based on non proliferation criteria, as they have already appeared several years ago. This work actually includes the following different aspects: identification of the non proliferation criterion defining this action; determination of the economical and technical goals to be reached; realization of research and development studies finalized in a full scale demonstration; transposition to an industrial and commercial level

DUSCOBS - a depleted-uranium silicate backfill for transport, storage, and disposal of spent nuclear fuel

International Nuclear Information System (INIS)

Forsberg, C.W.; Pope, R.B.; Ashline, R.C.; DeHart, M.D.; Childs, K.W.; Tang, J.S.

1995-01-01

A Depleted Uranium Silicate COntainer Backfill System (DUSCOBS) is proposed that would use small, isotopically-depleted uranium silicate glass beads as a backfill material inside storage, transport, and repository waste packages containing spent nuclear fuel (SNF). The uranium silicate glass beads would fill all void space inside the package including the coolant channels inside SNF assemblies. Based on preliminary analysis, the following benefits have been identified. DUSCOBS improves repository waste package performance by three mechanisms. First, it reduces the radionuclide releases from SNF when water enters the waste package by creating a local uranium silicate saturated groundwater environment that suppresses (1) the dissolution and/or transformation of uranium dioxide fuel pellets and, hence, (2) the release of radionuclides incorporated into the SNF pellets. Second, the potential for long-term nuclear criticality is reduced by isotopic exchange of enriched uranium in SNF with the depleted uranium (DU) in the glass. Third, the backfill reduces radiation interactions between SNF and the local environment (package and local geology) and thus reduces generation of hydrogen, acids, and other chemicals that degrade the waste package system. In addition, the DUSCOBS improves the integrity of the package by acting as a packing material and ensures criticality control for the package during SNF storage and transport. Finally, DUSCOBS provides a potential method to dispose of significant quantities of excess DU from uranium enrichment plants at potential economic savings. DUSCOBS is a new concept. Consequently, the concept has not been optimized or demonstrated in laboratory experiments

Design of a uranium-dioxide powder spheroidization system by plasma processing

Science.gov (United States)

Cavender, Daniel

The plasma spheroidization system (PSS) is the first process in the development of a tungsten-uranium dioxide (W-UO2) ceramic-metallic (cermet) fuel for nuclear thermal rocket (NTR) propulsion. For the purposes of fissile fuel retention, UO2 spheroids ranging in size from 50 - 100 micrometers (μm) in diameter will be encapsulated in a tungsten shell. The PSS produces spherical particles by melting angular stock particles in an argon-hydrogen plasma jet where they become spherical due to surface tension. Surrogate CeO 2 powder was used in place of UO2 for system and process parameter development. Stock and spheroidized powders were micrographed using optical and scanning electron microscopy and evaluated by statistical methods to characterize and compare the spherocity of pre and post process powders. Particle spherocity was determined by irregularity parameter. Processed powders showed a statistically significant improvement in spherocity, with greater that 60% of the examined particles having an irregularity parameter of equal to or lower than 1.2, compared to stock powder.

The migration of intra-granular fission gas bubbles in irradiated uranium dioxide

International Nuclear Information System (INIS)

Baker, C.

1977-05-01

The mobility of intragranular fission gas bubbles in uranium dioxide irradiated at 1600-1800 0 C has been studied following isothermal annealing at temperatures below 1600 0 C. The intragranular fission gas bubbles, average diameter approximately 2nm, are virtually immobile at temperatures below 1500 0 C. The bubbles have clean surfaces with no solid fission product contamination and are faceted to the highest observed irradiation temperature of 1800 0 C. This bubble faceting is believed to be a major cause of bubble immobility. In fuel operating below 1500 0 C the predominant mechanism allowing the growth of intragranular bubbles and the subsequent gas release must be the diffusion of dissolved gas atoms rather than the movement of entire intragranular bubbles. (author)

On the possibility of reprocessing of fuel elements of dispersion type with copper matrix by pyrochemical methods

International Nuclear Information System (INIS)

Vasin, B.D.; Ivanov, V.A.; Shchetinskij, A.V.; Vavilov, S.K.; Savochkin, Yu.P.; Bychkov, A.V.; Kormilitsyn, M.V.

2005-01-01

A consideration is given to pyrochemical processes suitable for separation of uranium dioxide from structural materials when reprocessing cermet type fuel elements. The estimation of the possibility to apply liquid antimony and bismuth, potassium and copper chlorides melts is made. The specimens compacted of copper and uranium dioxide powders in a stainless steel can are used as simulators of fuel element sections. It is concluded that the dissolution of structural materials in molten salts at the stage of uranium dioxide concentration is the process of choice for reprocessing of dispersion type fuel elements [ru

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

International Nuclear Information System (INIS)

Stern, V.H.

1991-08-01

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

Comparison of the Environment, Health, And Safety Characteristics of Advanced Thorium- Uranium and Uranium-Plutonium Fuel Cycles

Science.gov (United States)

Ault, Timothy M.

The environment, health, and safety properties of thorium-uranium-based (''thorium'') fuel cycles are estimated and compared to those of analogous uranium-plutonium-based (''uranium'') fuel cycle options. A structured assessment methodology for assessing and comparing fuel cycle is refined and applied to several reference fuel cycle options. Resource recovery as a measure of environmental sustainability for thorium is explored in depth in terms of resource availability, chemical processing requirements, and radiological impacts. A review of available experience and recent practices indicates that near-term thorium recovery will occur as a by-product of mining for other commodities, particularly titanium. The characterization of actively-mined global titanium, uranium, rare earth element, and iron deposits reveals that by-product thorium recovery would be sufficient to satisfy even the most intensive nuclear demand for thorium at least six times over. Chemical flowsheet analysis indicates that the consumption of strong acids and bases associated with thorium resource recovery is 3-4 times larger than for uranium recovery, with the comparison of other chemical types being less distinct. Radiologically, thorium recovery imparts about one order of magnitude larger of a collective occupational dose than uranium recovery. Moving to the entire fuel cycle, four fuel cycle options are compared: a limited-recycle (''modified-open'') uranium fuel cycle, a modified-open thorium fuel cycle, a full-recycle (''closed'') uranium fuel cycle, and a closed thorium fuel cycle. A combination of existing data and calculations using SCALE are used to develop material balances for the four fuel cycle options. The fuel cycle options are compared on the bases of resource sustainability, waste management (both low- and high-level waste, including used nuclear fuel), and occupational radiological impacts. At steady-state, occupational doses somewhat favor the closed thorium option while low

Study and simulation of the behaviour under irradiation of helium in uranium dioxide; Etude et modelisation du comportement sous irradiation de l'helium dans le dioxyde d'uranium

Energy Technology Data Exchange (ETDEWEB)

Martin, G

2007-06-15

Large quantities of helium are produced from {alpha}-decay of actinides in nuclear fuels during its in-pile operating and its storage. It is important to understand the behaviour of helium in these matrix in order to well simulate the evolution and the resistance of the fuel element. During this thesis, we have used nuclear reaction analyses (NRA) to follow the evolution of the helium implanted in polycrystalline and monocrystalline uranium dioxide (UO{sub 2}). An experimental rig was developed to follow the on-line helium release in UO{sub 2} and the evolution of {sup 3}He profiles as a function of annealing temperature. An automated procedure taking into account the evolution of the depth resolution was developed. Analyses performed with a nuclear microprobe allowed to characterise the spatial distribution of helium at the grain scale and to study the influence of the sample microstructure on the helium migration. This work put into evidence the particular role of grain boundaries and irradiation defects in the helium release process. The analyse of experimental results with a diffusion model corroborates these interpretations. It allowed to determine quantitatively physical properties that characterise the helium behaviour in uranium dioxide (diffusion coefficient, activation energy..). (author)

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

Energy Technology Data Exchange (ETDEWEB)

Mac Donald, Philip Elsworth

2002-09-01

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

Evaluation of plutonium, uranium, and thorium use in power reactor fuel cycles

International Nuclear Information System (INIS)

Kasten, P.R.; Homan, F.J.

1977-01-01

The increased cost of uranium and separative work has increased the attractiveness of plutonium use in both uranium and thorium fuel cycles in thermal reactors. A technology, fuel utilization, and economic evaluation is given for uranium and thorium fuel cycles in various reactor types, along with the use of plutonium and 238 U. Reactors considered are LWRs, HWRs, LWBRs, HTGRs, and FBRs. Key technology factors are fuel irradiation performance and associated physical property values. Key economic factors are unit costs for fuel fabrication and reprocessing, and for refabrication of recycle fuels; consistent cost estimates are utilized. In thermal reactors, the irradiation performance of ceramic fuels appears to be satisfactory. At present costs for uranium ore and separative work, recycle of plutonium with thorium rather than uranium is preferable from fuel utilization and economic viewpoints. Further, the unit recovery cost of plutonium is lower from LWR fuels than from natural-uranium HWR fuels; use of LWR product permits plutonium/thorium fueling to compete with uranium cycles. Converting uranium cycles to thorium cycles increases the energy which can be extracted from a given uranium resource. Thus, additional fuel utilization improvement can be obtained by fueling all thermal reactors with thorium, but this requires use of highly enriched uranium; use of 235 U with thorium is most economic in HTGRs followed by HWRs and then LWRs. Marked improvement in long-term fuel utilization can be obtained through high thorium loadings and short fuel cycle irradiations as in the LWBR, but this imposes significant economic penalties. Similar operating modes are possible in HWRs and HTGRs. In fast reactors, use of the plutonium-uranium cycle gives advantageous fuel resource utilization in both LMFBRs and GCFRs; use of the thorium cycle provides more negative core reactivity coefficients and more flexibility relative to use of recycle fuels containing uranium of less than 20

A kinetic study of the reaction of water vapor and carbon dioxide on uranium

International Nuclear Information System (INIS)

Santon, J.P.

1964-09-01

The kinetic study of the reaction of water vapour and carbon dioxide with uranium has been performed by thermogravimetric methods at temperatures between 160 and 410 deg G in the first case, 350 and 1050 deg C in the second: Three sorts of uranium specimens were used: uranium powder, thin evaporated films, and small spheres obtained from a plasma furnace. The experimental results led in the case of water vapour, to a linear rate of reaction controlled by diffusion at the lower temperatures, and by a surface reaction at the upper ones. In the case of carbon dioxide, a parabolic law has been found, controlled by diffusional processes. (author) [fr

Characterization of transport properties in uranium dioxide: the case of the oxygen auto-diffusion

International Nuclear Information System (INIS)

Fraczkiewicz, M.; Baldinozzi, G.

2008-01-01

Point defects in uranium dioxide which control the transport phenomena are still badly known. The aim of this work is to show how in carrying out several experimental techniques, it is possible to demonstrate both the existence and to determine the nature (charge and localization) of predominant defects responsible of the transport phenomena in a fluorite-type structure oxide. The oxygen diffusion in the uranium dioxide illustrates this. In the first part of this work, the accent is put on the electric properties of uranium dioxide and more particularly on the variation laws of the electric conductivity in terms of temperature, of oxygen potential and of the impurities amounts present in the material. These evolutions are connected to point and charged complex defects models and the pertinence of these models is discussed. Besides, it is shown how the electric conductivity measurements can allow to define oxygen potential domains in which the concentrations in electronic carriers are controlled. This characterization being made, it is shown that the determination of the oxygen intrinsic diffusion coefficient and particularly its dependence to the oxygen potential and to the amount of impurity, allows to determine the main defect responsible to the atomic diffusion as well as its nature and its charge. In the second part, the experimental techniques to determine the oxygen diffusion coefficient are presented: there are the isotopic exchange technique for introducing the tracer in the material, and two techniques to characterize the diffusion profiles (SIMS and NRA). Examples of preliminary results are given for mono and polycrystalline samples. At last, from this methodology on uranium dioxide, studies considered to quantify the thermal and physicochemical effects are presented. Experiments considered with the aim to characterize the radiation diffusion in uranium dioxide are presented too. (O.M.)

PHWR fuel fabrication with imported uranium - procedures and processes

International Nuclear Information System (INIS)

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

2010-01-01

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

Behaviour of HTGR coated fuel particles at high-temperature tests

International Nuclear Information System (INIS)

Chernikov, A.S.; Lyutikov, R.A.; Kurbakov, S.D.; Repnikov, V.M.; Khromonozhkin, V.V.; Soloviyov, G.I.

1990-01-01

At the temperature range 1200-2600 deg. C prereactor tests of TRISO fuel particles on the base of UO 2 , UC x O y and UO 2 +2Al 2 O 3 . SiO 2 kernels, and also fuel particle models with ZrC kernels were performed. Isothermal annealings carried out at temperatures of 1400-2600 deg. C, thermogradient ones at 1200-2200 deg. C (Δ T = 200-1200 deg. C/cm). It is shown that at heating to 2200 deg. C integrity of fuel particles is limited by different thermal expansion of PyC and SiC coatings, and also by thermal dissociation of SiC. At higher temperatures the failure is caused by development of high pressures within weakened fuel particles. It is found that uranium migration from alloyed fuel (UC x O y , UO 2 +2Al 2 O 3 .SiO 2 ) in the process of annealing is higher than that from UO 2 . (author)

Establishment of THERPRO Database and Estimation of the Effect of Fuel Burn-up on the Thermal Conductivity of Uranium Dioxide

International Nuclear Information System (INIS)

Lee, Hyun Seon

2005-02-01

Materials property data are an essential part of major disciplines in many engineering fields. To nuclear engineering, fundamental understanding of thermo-physical chemical mechanical properties of nuclear materials is very important. THERPRO data base that is re-designed and re-constructed through this study is a web-based on-line nuclear materials properties data base. For the future upgrade of the data base contemporary information technologies have been incorporated during the construction. Basically THERPRO data base has a hierarchical structure consisting of several levels: home page, element, compound, property, author, report, and bibliography level. All of data sets in each level are interconnected using network structure and thus every data can be easily retrieved including the bibliographical information by an appropriate query action. As a part of THERPRO DB utilization, the effect of fuel burn-up on the thermal conductivity of irradiated uranium dioxide is analyzed with the data contained in the data base as well as recent data published in the relevant journals. Their data are comparatively studied and the effect is estimated using FRAPCON-3 code with two in-pile data sets, BR-3 111i5 and Oconee rod 15309. The results show that the fuel center line temperature can differ 200 .deg. C∼400 .deg. C from thermal conductivity models depending on burn-up, which can significantly influence high burn-up fuel performance. In conclusion, it is demonstrated through this study that THERPRO data base can be a great utility for nuclear engineers and researchers, if appropriately utilized

FY16 Status Report for the Uranium-Molybdenum Fuel Concept

International Nuclear Information System (INIS)

Bennett, Wendy D.; Doherty, Ann L.; Henager, Charles H.; Lavender, Curt A.; Montgomery, Robert O.; Omberg, Ronald P.; Smith, Mark T.; Webster, Ryan A.

2016-01-01

The Fuel Cycle Research and Development program of the Office of Nuclear Energy has implemented a program to develop a Uranium-Molybdenum metal fuel for light water reactors. Uranium-Molybdenum fuel has the potential to provide superior performance based on its thermo-physical properties. With sufficient development, it may be able to provide the Light Water Reactor industry with a melt-resistant, accident-tolerant fuel with improved safety response. The Pacific Northwest National Laboratory has been tasked with extrusion development and performing ex-reactor corrosion testing to characterize the performance of Uranium-Molybdenum fuel in both these areas. This report documents the results of the fiscal year 2016 effort to develop the Uranium-Molybdenum metal fuel concept for light water reactors.

FY16 Status Report for the Uranium-Molybdenum Fuel Concept

Energy Technology Data Exchange (ETDEWEB)

Bennett, Wendy D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Doherty, Ann L. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Henager, Charles H. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Lavender, Curt A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Montgomery, Robert O. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Omberg, Ronald P. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Smith, Mark T. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Webster, Ryan A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2016-09-22

The Fuel Cycle Research and Development program of the Office of Nuclear Energy has implemented a program to develop a Uranium-Molybdenum metal fuel for light water reactors. Uranium-Molybdenum fuel has the potential to provide superior performance based on its thermo-physical properties. With sufficient development, it may be able to provide the Light Water Reactor industry with a melt-resistant, accident-tolerant fuel with improved safety response. The Pacific Northwest National Laboratory has been tasked with extrusion development and performing ex-reactor corrosion testing to characterize the performance of Uranium-Molybdenum fuel in both these areas. This report documents the results of the fiscal year 2016 effort to develop the Uranium-Molybdenum metal fuel concept for light water reactors.

Process for the preparation of uranium dioxide

International Nuclear Information System (INIS)

Watt, G.W.; Baugh, D.W. Jr.

1977-01-01

An actinide dioxide, e.g., uranium dioxide, plutonium dioxide, neptunium dioxide, etc., is prepared by reacting the actinide nitrate hexahydrate with sodium dithionite as a first step; the reaction product from this first step is a novel composition of matter comprising the actinide sulfite tetrahydrate. The reaction product resulting from this first step is then converted to the actinide dioxide by heating it in the absence of an oxygen-containing atmosphere (e.g., nitrogen) to a temperature of about 500 0 to about 950 0 C for about 15 to about 135 minutes. If the reaction product resulting from the first step is, prior to carrying out the second heating step, exposed to an oxygen-containing atmosphere such as air, the resultant product is a novel composition of matter comprising the actinide oxysulfite tetrahydrate which can also be readily converted to the actinide dioxide by heating it in the absence of an oxygen-containing atmosphere (e.g., nitrogen) at a temperature of about 400 0 to about 900 0 C for about 30 to about 150 minutes. Further, the actinide oxysulfite tetrahydrate can be partially dehydrated at reduced pressures (and in the presence of a suitable dehydrating agent such as phosphorus pentoxide). The partially dehydrated product may be readily converted to the dioxide form by heating it in the absence of an oxygen-containing atmosphere (e.g., nitrogen) at a temperature of about 500 0 to about 900 0 C for about 30 to about 150 minutes. 16 claims

Synthesis of uranium metal using laser-initiated reduction of uranium tetrafluoride by calcium metal

International Nuclear Information System (INIS)

West, M.H.; Martinez, M.M.; Nielsen, J.B.; Court, D.C.; Appert, Q.D.

1995-09-01

Uranium metal has numerous uses in conventional weapons (armor penetrators) and nuclear weapons. It also has application to nuclear reactor designs utilizing metallic fuels--for example, the former Integral Fast Reactor program at Argonne National Laboratory. Uranium metal also has promise as a material of construction for spent-nuclear-fuel storage casks. A new avenue for the production of uranium metal is presented that offers several advantages over existing technology. A carbon dioxide (CO 2 ) laser is used to initiate the reaction between uranium tetrafluoride (UF 4 ) and calcium metal. The new method does not require induction heating of a closed system (a pressure vessel) nor does it utilize iodine (I 2 ) as a chemical booster. The results of five reductions of UF 4 , spanning 100 to 200 g of uranium, are evaluated, and suggestions are made for future work in this area

Development of Diffusion barrier coatings and Deposition Technologies for Mitigating Fuel Cladding Chemical Interactions (FCCI)

Energy Technology Data Exchange (ETDEWEB)

Sridharan, Kumar; Allen, Todd; Cole, James

2013-02-27

The goal of this project is to develop diffusion barrier coatings on the inner cladding surface to mitigate fuel-cladding chemical interaction (FCCI). FCCI occurs due to thermal and radiation enhanced inter-diffusion between the cladding and fuel materials, and can have the detrimental effects of reducing the effective cladding wall thickness and lowering the melting points of the fuel and cladding. The research is aimed at the Advanced Burner Reactor (ABR), a sodium-cooled fast reactor, in which higher burn-ups will exacerbate the FCCI problem. This project will study both diffusion barrier coating materials and deposition technologies. Researchers will investigate pure vanadium, zirconium, and titanium metals, along with their respective oxides, on substrates of HT-9, T91, and oxide dispersion-strengthened (ODS) steels; these materials are leading candidates for ABR fuel cladding. To test the efficacy of the coating materials, the research team will perform high-temperature diffusion couple studies using both a prototypic metallic uranium fuel and a surrogate the rare-earth element lanthanum. Ion irradiation experiments will test the stability of the coating and the coating-cladding interface. A critical technological challenge is the ability to deposit uniform coatings on the inner surface of cladding. The team will develop a promising non-line-of-sight approach that uses nanofluids . Recent research has shown the feasibility of this simple yet novel approach to deposit coatings on test flats and inside small sections of claddings. Two approaches will be investigated: 1) modified electrophoretic deposition (MEPD) and 2) boiling nanofluids. The coatings will be evaluated in the as-deposited condition and after sintering.

Development of an alternative process for recovery of uranium from rejected plates in the manufacture of MTR type fuel elements

International Nuclear Information System (INIS)

Flores Gonzalez, Jocelyn Natalia

2011-01-01

This work discusses the recovery of enriched uranium in U 235 , from fuel plates rejected during the fuel elements manufacturing process for the La Reina Nuclear Studies Center, RECH-1, CCHEN. The plates have an aluminum based alloy coating, AISI-SAE 6061, with U 3 Si 2 powder distributed evenly inside and dispersed in an aluminum matrix. The high cost of enriched uranium means that it must be recovered from plates rejected in the production process because of non-compliance with the plate specifications, and also because some of them undergo destructive testing, to measure the aluminum coating's thickness on each side of the plate. The thickness of the uranium nucleus is measured as well and the size of the defects on the ends of the plate such as 'dog bone' and 'fish tail', that is, for the purposes of quality control. The first step in the process is carried out by dissolving the aluminum in a hot solution of NaOH in order to release the uranium silicide powder that is insoluble in the soda. A second step involves dissolving the uranium silicide in a hot HNO 3 solution, followed by washing and filtering, and then extracting the SX and analyzing its behavior during this stage. During the process 98.9% of the uranium is recovered together with a solution that is enough for the SX process given the experiences that were carried out in the extraction stage

Fuel Cycle Impacts of Uranium-Plutonium Co-extraction

International Nuclear Information System (INIS)

Taiwo, Temitope; Szakaly, Frank; Kim, Taek-Kyum; Hill, Robert

2008-01-01

A systematic investigation of the impacts of uranium and plutonium co-extraction during fuel separations on reactor performance and fuel cycle has been performed. Proliferation indicators, critical mass and radiation source levels of the separation products or fabricated fuel, were also evaluated. Using LWR-spent-uranium-based MOX fuel instead of natural-uranium-based fuel in a PWR MOX core requires a higher initial plutonium content (∼1%), and results in higher Np-237 content (factor of 5) in the spent fuel, and less consumption of Pu-238 (20%) and Am-241 (14%), indicating a reduction in the effective repository space utilization. Additionally, minor actinides continue to accumulate in the fuel cycle, and thus a separate solution is required for them. Differences were found to be quite smaller (∼0.4% in initial transuranics) between the equilibrium cycles of advanced fast reactor cores using spent and depleted uranium for make-up, in additional to transuranics. The critical masses of the co-extraction products were found to be higher than for weapons-grade plutonium (WG-Pu) and the decay heat and radiation sources of the materials (products) were also found to be generally higher than for WG-Pu in the transuranics content range of 10% to 100% in the heavy-metal. (authors)

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

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)

Investigating the structural changes of uranium dioxide dependent on additives, Phase I - Uranium-oxide system from structural-phase aspect

International Nuclear Information System (INIS)

Manojlovic, Lj.

1962-12-01

Having in mind the complex structure of the system uranium-oxygen, and that experimental studies of this system lead to controversial conclusions, an extensive review and analysis of the papers published on this subject were needed. This review wold be very useful for interpreting the expected structural changes of the uranium dioxide dependent on the additives

SULPHUR DIOXIDE LEACHING OF URANIUM CONTAINING MATERIAL

Science.gov (United States)

Thunaes, A.; Rabbits, F.T.; Hester, K.D.; Smith, H.W.

1958-12-01

A process is described for extracting uranlum from uranium containing material, such as a low grade pitchblende ore, or mill taillngs, where at least part of the uraniunn is in the +4 oxidation state. After comminuting and magnetically removing any entrained lron particles the general material is made up as an aqueous slurry containing added ferric and manganese salts and treated with sulfur dioxide and aeration to an extent sufficient to form a proportion of oxysulfur acids to give a pH of about 1 to 2 but insufficient to cause excessive removal of the sulfur dioxide gas. After separating from the solids, the leach solution is adjusted to a pH of about 1.25, then treated with metallic iron in the presence of a precipitant such as a soluble phosphate, arsonate, or fluoride.

Novel ceramic coatings for containment of uranium and reactive molten metals

International Nuclear Information System (INIS)

Sreekumar, K.P.; Satpute, R.U.; Ramanathan, S.; Thiyagarajan, T.K.; Padmanabhan, P.V.A.; Kutty, T.R.G.

2005-01-01

Plasma sprayed aluminium oxide coatings, which are currently used for casting uranium metal are, however, not suitable for long duration handling of molten uranium and is also unstable under reducing conditions. Yttrium oxide and rare earth phosphates are suggested as promising materials for prevention of high temperature corrosion by molten metals. The present paper reports research efforts directed towards development of plasma sprayed coatings of yttria and lanthanum phosphate. Thermal spray grade powders of yttrium oxide and lanthanum phosphate, synthesized using locally available raw materials have been used as feedstock powders for plasma spray deposition. The coatings have been deposited using the indigenously developed 40 kW atmospheric plasma spray system and have been characterized. Results of preliminary experiments on compatibility of yttria and lanthanum phosphate with molten uranium are quite encouraging. (author)

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

Energy Technology Data Exchange (ETDEWEB)

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

2017-11-01

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

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

International Nuclear Information System (INIS)

Goncalves, Isadora C.; Wichrowski, Caio C.; Oliveira, Claudio L. de; Vellozo, Sergio O.; Baptista, Camila O.

2017-01-01

It is known that isotope "2"3"2thorium is a fertile nuclide with the ability to convert into "2"3"3uranium, a potentially fissile isotope, after absorbing a neutron. As there is a large stock of available thorium in the world, this element shows great promise in mitigate the world energy crisis, more particularly in the problem of uranium scarcity, besides being an alternative nuclear fuel for those currently used in reactors, and yet presenting advantages as an option for the non-proliferation movement, among others. In this study, the analysis of the remaining nuclides of burnup was carried out for the core configuration of a PWR (pressurized water reactor) reactor, specifically the Angra 2 reactor, using only uranium dioxide, its current configuration, and in different configurations including a mixed oxide of uranium and thorium in three concentrations, allowing a preliminary assessment of the feasibility of the modification of the fuel, the resulting production of "2"3"3uranium, the emergence of "2"3"1protactinium (an isotope that only occurs as a fission product of "2"3"2Th) resulting from burning. The study was carried out using data obtained from FSAR (Final Safety Analysis Report) of Angra 2, using the SCALE 6.1, a modeling and simulation nuclear code, especially its ORIGEN-ARP module, which analyzes the depletion of isotopes presents in a reactor. (author)

Research Establishment progress report 1978 - uranium fuel cycle

International Nuclear Information System (INIS)

1978-12-01

A report of research programs continuing in the following areas is presented: mining and treatment of uranium ores, uranium enrichment, waste treatment, reprocessing and the uranium fuel cycle. Staff responsible for each project are indicated

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

International Nuclear Information System (INIS)

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

2010-01-01

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

Nuclear fuel rods

International Nuclear Information System (INIS)

Wada, Toyoji.

1979-01-01

Purpose: To remove failures caused from combination of fuel-cladding interactions, hydrogen absorptions, stress corrosions or the likes by setting the quantity ratio of uranium or uranium and plutonium relative to oxygen to a specific range in fuel pellets and forming a specific size of a through hole at the center of the pellets. Constitution: In a fuel rods of a structure wherein fuel pellets prepared by compacting and sintering uranium dioxide, or oxide mixture consisting of oxides of plutonium and uranium are sealed with a zirconium metal can, the ratio of uranium or uranium and plutonium to oxygen is specified as 1 : 2.01 - 1 : 2.05 in the can and a passing hole of a size in the range of 15 - 30% of the outer diameter of the fuel pellet is formed at the center of the pellet. This increases the oxygen partial pressure in the fuel rod, oxidizes and forms a protection layer on the inner surface of the can to control the hydrogen absorption and stress corrosion. Locallized stress due to fuel cladding interaction (PCMI) can also be moderated. (Horiuchi, T.)

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

Energy Technology Data Exchange (ETDEWEB)

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

2012-07-30

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

Operation of Nuclear Fuel Based on Reprocessed Uranium for VVER-type Reactors in Competitive Nuclear Fuel Cycles

Energy Technology Data Exchange (ETDEWEB)

Troyanov, V.; Molchanov, V.; Tuzov, A. [TVEL Corporation, 49 Kashirskoe shosse, Moscow 115409 (Russian Federation); Semchenkov, Yu.; Lizorkin, M. [RRC ' Kurchatov Institute' (Russian Federation); Vasilchenko, I.; Lushin, V. [OKB ' Gidropress' (Russian Federation)

2009-06-15

Current nuclear fuel cycle of Russian nuclear power involves reprocessed low-enriched uranium in nuclear fuel production for some NPP units with VVER-type LWR. This paper discusses design and performance characteristics of commercial nuclear fuel based on natural and reprocessed uranium. It presents the review of results of commercial operation of nuclear fuel based on reprocessed uranium on Russian NPPs-unit No.2 of Kola NPP and unit No.2 of Kalinin NPP. The results of calculation and experimental validation of safe fuel operation including necessary isotope composition conformed to regulation requirements and results of pilot fuel operation are also considered. Meeting the customer requirements the possibility of high burn-up achieving was demonstrated. In addition the paper compares the characteristics of nuclear fuel cycles with maximum length based on reprocessed and natural uranium considering relevant 5% enrichment limitation and necessity of {sup 236}U compensation. The expedience of uranium-235 enrichment increasing over 5% is discussed with the aim to implement longer fuel cycles. (authors)

Synthesis and preservation of graphene-supported uranium dioxide nanocrystals

Energy Technology Data Exchange (ETDEWEB)

Ma, Hanyu [Department of Civil and Environmental Engineering and Earth Sciences, University of Notre Dame, 156 Fitzpatrick Hall, Notre Dame, IN 46556 (United States); Wang, Haitao [Department of Civil and Environmental Engineering and Earth Sciences, University of Notre Dame, 156 Fitzpatrick Hall, Notre Dame, IN 46556 (United States); Department of Civil, Environmental, and Construction Engineering, Texas Tech University, 911 Boston Ave., Lubbock, TX 79409 (United States); Burns, Peter C. [Department of Civil and Environmental Engineering and Earth Sciences, University of Notre Dame, 156 Fitzpatrick Hall, Notre Dame, IN 46556 (United States); Department of Chemistry and Biochemistry, University of Notre Dame, 251 Nieuwland Science Hall, Notre Dame, IN 46556 (United States); McNamara, Bruce K.; Buck, Edgar C. [Nuclear Chemistry & Engineering Group, Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, WA 99352 (United States); Na, Chongzheng, E-mail: chongzheng.na@gmail.com [Department of Civil and Environmental Engineering and Earth Sciences, University of Notre Dame, 156 Fitzpatrick Hall, Notre Dame, IN 46556 (United States); Department of Civil, Environmental, and Construction Engineering, Texas Tech University, 911 Boston Ave., Lubbock, TX 79409 (United States)

2016-07-15

Graphene-supported uranium dioxide (UO{sub 2}) nanocrystals are potentially important fuel materials. Here, we investigate the possibility of synthesizing graphene-supported UO{sub 2} nanocrystals in polar ethylene glycol compounds by the polyol reduction of uranyl acetylacetone under boiling reflux, thereby enabling the use of an inexpensive graphene precursor graphene oxide into a one-pot process. We show that triethylene glycol is the most suitable solvent with an appropriate reduction potential for producing nanometer-sized UO{sub 2} crystals compared to monoethylene glycol, diethylene glycol, and polyethylene glycol. Graphene-supported UO{sub 2} nanocrystals synthesized with triethylene glycol show evidence of heteroepitaxy, which can be beneficial for facilitating heat transfer in nuclear fuel particles. Furthermore, we show that graphene-supported UO{sub 2} nanocrystals synthesized by polyol reduction can be readily stored in alcohols, impeding oxidation from the prevalent oxygen in air. Together, these methods provide a facile approach for preparing and storing graphene-supported UO{sub 2} nanocrystals for further investigation and development under ambient conditions. - Highlights: • UO{sub 2} nanocrystals are synthesized using polyol reduction method. • Triethylene glycol is the best reducing agent for nano-sized UO{sub 2} crystals. • UO{sub 2} nanocrystals grow on graphene through heteroepitaxy. • Graphene-supported UO{sub 2} nanocrystals can be stored in alcohols to prevent oxidation.

Research on calculation of mixing fraction for natural uranium equivalent fuel

International Nuclear Information System (INIS)

Huang Shien; Wang Lianjie; Wei Yanqin; Li Qing; Zheng Jiye

2013-01-01

Based on the first-order perturbation theory and reasonable approximations, the calculation method of recycled uranium (RU) and depleted uranium (DU) mixing fraction for natural uranium equivalent (NUE) fuel was studied, so the equivalence between NUE fuel and natural uranium (NU) fuel was assured. The adopted calculation method accurately takes the variation of micro cross sections alone with fuel depletion into account. A computer code named ALPHA was programmed to execute the calculation procedure. Then the ALPHA code and the WIMS-AECL code compose a processing system, which is applicable to the mixing fraction calculation for heavy water reactor NUE fuel. The validation shows that the processing system can accurately calculate the mixing fraction for NUE fuel. (authors)

Evaluation of Hydrothermally Synthesized Uranium Dioxide for Novel Semiconductor Applications

Science.gov (United States)

2016-08-29

Technology Air University Air Education and Training Command In Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy ...Senanayake, G. Waterhouse, A. Chan, T. Madey, D. Mullins and H. Idriss, "Probing Surface Oxidation of Reduced Uranium Dioxide Thin Film Using

Uranium Fuel Plant. Applicants environmental report

International Nuclear Information System (INIS)

1975-05-01

The Uranium Fuel Plant, located at the Cimarron Facility, was constructed in 1964 with operations commencing in 1965 in accordance with License No. SNM-928, Docket No. 70-925. The plant has been in continuous operation since the issuance of the initial license and currently possesses contracts extending through 1978, for the production of nuclear fuels. The Uranium Plant is operated in conjunction with the Plutonium Facility, each sharing common utilities and sanitary wastes disposal systems. The operation has had little or no detrimental ecological impact on the area. For the operation of the Uranium Fuel Fabrication Plant, initial equipment provided for the production of UO 2 , UF 4 , uranium metal and recovery of scrap materials. In 1968, the plant was expanded by increasing the UO 2 and pellet facilities by the installation of another complete production line for the production of fuel pellets. In 1969, fabrication facilities were added for the production of fuel elements. Equipment initially installed for the recovery of fully enriched scrap has not been used since the last work was done in 1970. Economically, the plant has benefited the Logan County area, with approximately 104 new jobs with an annual payroll of approximately $1.3 million. In addition, $142,000 is annually paid in taxes to state, local and federal governments, and local purchases amount to approximately $1.3 million. This was all in land that was previously used for pasture land, with a maximum value of approximately 37,000 dollars. Environmental effects of plant operation have been minimal. A monitoring and measurement program is maintained in order to ensure that the ecology of the immediate area is not affected by plant operations

Fabrication procedures for manufacturing high uranium concentration dispersion fuel elements

International Nuclear Information System (INIS)

Souza, J.A.B.; Durazzo, M.

2010-01-01

IPEN developed and made available for routine production the technology for manufacturing dispersion type fuel elements for use in research reactors. However, the fuel produced at IPEN is limited to the uranium concentration of 3.0 gU/cm 3 by using the U 3 Si 2 -Al dispersion. Increasing the uranium concentration of the fuel is interesting by the possibility of increasing the reactor core reactivity and lifetime of the fuel. It is possible to increase the concentration of uranium in the fuel up to the technological limit of 4.8 gU/cm 3 for the U 3 Si 2 -Al dispersion, which is well placed around the world. This new fuel will be applicable in the new Brazilian-Multipurpose Reactor RMB. This study aimed to develop the manufacturing process of high uranium concentration fuel, redefining the procedures currently used in the manufacture of IPEN. This paper describes the main procedures adjustments that will be necessary. (author)

Fabrication procedures for manufacturing high uranium concentration dispersion fuel elements

Energy Technology Data Exchange (ETDEWEB)

Souza, Jose Antonio Batista de; Durazzo, Michelangelo, E-mail: jasouza@ipen.br [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

2011-07-01

IPEN developed and made available for routine production the technology for manufacturing dispersion type fuel elements for use in research reactors. However, the fuel produced at IPEN is limited to the uranium concentration of 3.0 g U/c m3 by using the U{sub 3}Si{sub 2}-Al dispersion. Increasing the uranium concentration of the fuel is interesting by the possibility of increasing the reactor core reactivity and lifetime of the fuel. It is possible to increase the concentration of uranium in the fuel up to the technological limit of 4.8 g U/c m3 for the U{sub 3}Si{sub 2}-Al dispersion, which is well placed around the world. This new fuel will be applicable in the new Brazilian- Multipurpose Reactor RMB. This study aimed to develop the manufacturing process of high uranium concentration fuel, redefining the procedures currently used in the manufacture of IPEN. This paper describes the main procedures adjustments that will be necessary. (author)

Security of supply of uranium as nuclear fuel

International Nuclear Information System (INIS)

Guzman Gomez-Selles, L.

2011-01-01

When we talk about Sustainability related to nuclear fuel, the first concern that comes to our mind is about the possibility of having guarantees on the uranium supply for a sufficient period of time. In this paper we are going to analyze the last Reserves data published by the OCD's Red Book and also how the Reserve concept in fully linked to the uranium price. Additionally, it is demonstrated how the uranium Security of supply is guaranteed for, at least, the next 100 years. finally, some comments are made regarding other sources of nuclear fuel as it is the uranium coming from the phosphates or the thorium. (Author)

Evaluation of refractory-metal-clad uranium nitride and uranium dioxide fuel pins after irradiation for times up to 10 450 hours at 990 C

Science.gov (United States)

Bowles, K. J.; Gluyas, R. E.

1975-01-01

The effects of some materials variables on the irradiation performance of fuel pins for a lithium-cooled space power reactor design concept were examined. The variables studied were UN fuel density, fuel composition, and cladding alloy. All pins were irradiated at about 990 C in a thermal neutron environment to the design fuel burnup. An 85-percent dense UN fuel gave the best overall results in meeting the operational goals. The T-111 cladding on all specimens was embrittled, possibly by hydrogen in the case of the UN fuel and by uranium and oxygen in the case of the UO2 fuel. Tests with Cb-1Zr cladding indicate potential use of this cladding material. The UO2 fueled specimens met the operational goals of less than 1 percent cladding strain, but other factors make UO2 less attractive than low-density UN for the contemplated space power reactor use.

Polarographic determination of uranium dioxide stoichiometry

International Nuclear Information System (INIS)

Viguie, J.; Uny, G.

1966-10-01

The method described allows the determination of small deviations from stoichiometry for uranium dioxide. It was applied to the study of surface oxidation of bulk samples. The sample is dissolved in phosphoric acid under an argon atmosphere; U(VI) is determined by polarography in PO 4 H 3 4.5 N - H 2 SO 4 4 N. U(IV) is determined by potentiometry. The detection limit is UO 2,0002 . The accuracy for a single determination at the 95% confidence level is ±20 per cent for samples with composition included between UO 2,001 and UO 2,01 . (authors) [fr

Development of high uranium-density fuels for use in research reactors

International Nuclear Information System (INIS)

Ugajin, Mitsuhiro; Akabori, Mitsuo; Itoh, Akinori

1996-01-01

The uranium silicide U 3 Si 2 possesses uranium density 11.3 gU/cm 3 with a congruent melting point of 1665degC, and is now successfully in use as a research reactor fuel. Another uranium silicide U 3 Si and U 6 Me-type uranium alloys (Me=Fe,Mn,Ni) have been chosen as new fuel materials because of the higher uranium densities 14.9 and 17.0 gU/cm 3 , respectively. Experiments were carried out to fabricate miniature aluminum-dispersion plate-type and aluminum-clad disk-type fuels by using the conventional picture-frame method and a hot-pressing technique, respectively. These included the above-mentioned new fuel materials as well as U 3 Si 2 . Totally 14 miniplates with uranium densities from 4.0 to 6.3 gU/cm 3 of fuel meat were prepared together with 28 disk-type fuel containing structurally-modified U 3 Si, and subjected to the neutron irradiation in JMTR (Japan Materials Testing Reactor). Some results of postirradiation examinations are presented. (author)

Nuclear fuel cycle head-end enriched uranium purification and conversion into metal

International Nuclear Information System (INIS)

Bonini, A.; Cabrejas, J.; Lio, L. de; Dell'Occhio, L.; Devida, C.; Dupetit, G.; Falcon, M.; Gauna, A.; Gil, D.; Guzman, G.; Neuringer, P.; Pascale, A.; Stankevicius, A.

1998-01-01

The CNEA (Comision Nacional de Energia Atomica - Argentina) operated two facilities at the Ezeiza Atomic Center which supply purified enriched uranium employed in the production of nuclear fuels. At one of those facilities, the Triple Height Laboratory scraps from the production of MTR type fuel elements (mainly out of specification U 3 O 8 plates or powder) are purified to nuclear grade. The purification is accomplished by a solvent extraction process. The other facility, the Enriched Uranium Laboratory produces 90% enriched uranium metal to be used in Mo 99 production (originally the uranium was used for the manufacture of MTR fuel elements made of aluminium-uranium alloy). This laboratory also provided metallic uranium with a lower enrichment (20%) for a first uranium-silicon testing fuel element, and in the near future it is going to recommence 20% enriched uranium related activities in order to provide the metal for the silicon-based fuel elements production (according to the policy of enrichment reduction for MTR reactors). (author)

Matpro--version 10: a handbook of materials properties for use in the analysis of light water reactor fuel rod behavior

International Nuclear Information System (INIS)

Reymann, G.A.

1978-02-01

The materials properties correlations and computer subcodes (MATPRO--Version 10) developed for use with various LWR fuel rod behavior analytical programs at the Idaho National Engineering Laboratory are described. Formulations of fuel rod material properties, which are generally semiempirical in nature, are presented for uranium dioxide and mixed uranium--plutonium dioxide fuel, zircaloy cladding, and fill gas mixtures

MATPRO-Version 11: a handbook of materials properties for use in the analysis of light water reactor fuel rod behavior

International Nuclear Information System (INIS)

Hagrman, D.L.; Reymann, G.A.

1979-02-01

This handbook describes the materials properties correlations and computer subcodes (MATPRO-Version 11) developed for use with various LWR fuel rod behavior analytical programs at the Idaho National Engineering Laboratory. Formulations of fuel rod material properties, which are generally semiempirical in nature, are presented for uranium dioxide and mixed uranium--plutonium dioxide fuel, zircaloy cladding, and fill gas mixtures

MATPRO-Version 11: a handbook of materials properties for use in the analysis of light water reactor fuel rod behavior

Energy Technology Data Exchange (ETDEWEB)

Hagrman, D.L.; Reymann, G.A. (comps.)

1979-02-01

This handbook describes the materials properties correlations and computer subcodes (MATPRO-Version 11) developed for use with various LWR fuel rod behavior analytical programs at the Idaho National Engineering Laboratory. Formulations of fuel rod material properties, which are generally semiempirical in nature, are presented for uranium dioxide and mixed uranium--plutonium dioxide fuel, zircaloy cladding, and fill gas mixtures.

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

Energy Technology Data Exchange (ETDEWEB)

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

2013-02-01

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

Thorium dioxide: properties and nuclear applications

International Nuclear Information System (INIS)

Belle, J.; Berman, R.M.

1984-01-01

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

Thorium dioxide: properties and nuclear applications

Energy Technology Data Exchange (ETDEWEB)

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

1984-01-01

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

Radioactive decay properties of CANDU fuel. Volume 1: the natural uranium fuel cycle

International Nuclear Information System (INIS)

Clegg, L.J.; Coady, J.R.

1977-01-01

The computer code CANIGEN was used to obtain the mass, activity, decay heat and toxicity of CANDU fuel and its component isotopes. Data are also presented on gamma spectra and neutron emissions. Part 1 presents these data for unirradiated fuel, uranium ore and uranium mill tailings. In Part 2 they have been computed for fuel irradiated to levels of burnup ranging from 140 GJ/kg U to 1150 GJ/kg U. (author)

Metallic uranium as fuel for fast reactors

International Nuclear Information System (INIS)

Moura Neto, C. de

1988-01-01

This paper presents a first overview of the use of metallic uranium and its alloys as an option for fuel for rapid reactors. Aspects are discussed concerning uranium alloys which present high solubility in the gamma phase. (author)

Research on using depleted uranium as nuclear fuel for HWR

International Nuclear Information System (INIS)

Zhang Jiahua; Chen Zhicheng; Bao Borong

1999-01-01

The purpose of our work is to find a way for application of depleted uranium in CANDU reactor by using MOX nuclear fuel of depleted U and Pu instead of natural uranium. From preliminary evaluation and calculation, it was shown that MOX nuclear fuel consisting of depleted uranium enrichment tailings (0.25% 235 U) and plutonium (their ratio 99.5%:0.5%) could replace natural uranium in CANDU reactor to sustain chain reaction. The prospects of application of depleted uranium in nuclear energy field are also discussed

Advanced Characterization Techniques for Silicon Carbide and Pyrocarbon Coatings on Fuel Particles for High Temperature Reactors (HTR)

Energy Technology Data Exchange (ETDEWEB)

Basini, V.; Charollais, F. [CEA Cadarache, DEN/DEC/SPUA, BP 1, 13108 St Paul Lez Durance (France); Dugne, O. [CEA Marcoule, DEN/DTEC/SCGS BP 17171 30207 Bagnols sur Ceze (France); Garcia, C. [Laboratoire des Composites Thermostructuraux (LCTS), UMR CNRS 5801, 3 allee de La Boetie, 33600 Pessac (France); Perez, M. [CEA Grenoble DRT/DTH/LTH, 17 rue des Martyrs, 38054 Grenoble cedex 9 (France)

2008-07-01

Cea and AREVA NP have engaged an extensive research and development program on HTR (high temperature reactor) fuel. The improving of safety of (very) high temperature reactors (V/HTR) is based on the quality of the fuel particles. This requires a good knowledge of the properties of the four-layers TRISO particles designed to retain the uranium and fission products during irradiation or accident conditions. The aim of this work is to characterize exhaustively the structure and the thermomechanical properties of each unirradiated layer (silicon carbide and pyrocarbon coatings) by electron microscopy (SEM, TEM), selected area electronic diffraction (SEAD), thermo reflectance microscopy and nano-indentation. The long term objective of this study is to define pertinent parameters for fuel performance codes used to better understand the thermomechanical behaviour of the coated particles. (authors)

Studies on yttrium oxide coatings for corrosion protection against molten uranium

International Nuclear Information System (INIS)

Chakravarthy, Y.; Bhandari, Subhankar; Pragatheeswaran; Thiyagarajan, T.K.; Ananthapadmanabhan, P.V.; Das, A.K.; Kumar, Jay; Kutty, T.R.G.

2012-01-01

Yttrium oxide is resistant to corrosion by molten uranium and its alloys. Yttrium oxide is recommended as a protective oxide layer on graphite and metal components used for melting and processing uranium and its alloys. This paper presents studies on the efficacy of plasma sprayed yttrium oxide coatings for barrier applications against molten uranium

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

International Nuclear Information System (INIS)

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

1988-11-01

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

Uranium conversion; Urankonvertering

Energy Technology Data Exchange (ETDEWEB)

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

2006-03-15

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

Fuel development for reactors of new generation in Ukraine

International Nuclear Information System (INIS)

Odeychuk, N.P.

2006-01-01

elements development with fuel on a basis: Metal: uranium, alloys of uranium; Ceramic: uranium dioxide, thorium dioxide, uranium carbonitride, uranium oxycarbide, mixed oxide of uranium and thorium. The special attention is given to discussion of the basic technological schemes of reception of the fuel microspheres, coated particles and spherical fuel elements for HTGR. Features of reception carbongraphite materials and products by the methods of volumetric gas-phase condensation of porous preparations by pyrocarbon are considered. Results of investigations of the basic fuel elements characteristics and their components, materials and products with pyrocarbon binding, including in conditions of reactor irradiations are discussed. The review concerning the experience of the development the fuel elements with fuel based on metal uranium is given. In NSC KIPT constructions and manufacturing techniques of components for active zones of new perspective directions of atomic engineering are created and proved, also was laid the foundation for the base design and technological decisions for the fourth generation nuclear reactors

Basic research on high-uranium density fuels for research and test reactors

International Nuclear Information System (INIS)

Ugajin, M.; Itoh, A.; Akabori, M.

1992-01-01

High-uranium density fuels, uranium silicides (U 3 Si 2 , U 3 Si) and U 6 Me-type uranium alloys (Me = Fe, Mn, Ni), were prepared and examined metallurgically as low-enriched uranium (LEU) fuels for research and test reactors. Miniature aluminum-dispersion plate-type fuel (miniplate) and aluminum-clad disk-type fuel specimens were fabricated and subjected to the neutron irradiation in JMTR (Japan Materials Testing Reactor). Fuel-aluminum compatibility tests were conducted to elucidate the extent of reaction and to identify reaction products. The relative stability of the fuels in an aluminum matrix was established at 350degC or above. Experiments were also performed to predict the chemical form of the solid fission-products in the uranium silicide (U 3 Si 2 ) simulating a high burnup anticipated for reactor service. (author)

Method to determine the thermal conductivity of uranium dioxide and the surface conductance at the cladding-core interface from internal reactions

Energy Technology Data Exchange (ETDEWEB)

Tsykanov, V A; Samsonov, B F; Spiridonov, Yu G; Fomin, N A

1975-01-01

A method is given for determining the temperature-dependent thermal conductivity of uranium dioxide and the contact conductance of the gas gap between the core and cladding of a fuel element. These quantities should be determined on various samples with different diameters. A method is described for determining the heat-production rate of a fuel element to within 1.5 to 2.5 percent. The method is based on using a calibrated electric heater and a sensor to measure the specific energy evolution from reactor gamma-radiation. The total errors in determining the thermal conductivity and the contact conductance do not exceed 4.5 and 8 percent, respectively.

High-uranium-loaded U3O8--Al fuel element development program

International Nuclear Information System (INIS)

Martin, M.M.

1978-01-01

The High-Uranium-Loaded U 3 O 8 --Al Fuel Development Program supports Argonne National Laboratory efforts to develop high-uranium-density research and test reactor fuel to accommodate use of low-uranium enrichment. The goal is to fuel most research and test reactors with uranium of less than 20% enrichment for the purpose of lowering the potential for diversion of highly-enriched material for nonpeaceful usages

Romania, producer and consumer of nuclear fuel

International Nuclear Information System (INIS)

Iuhas, Tiberius

1998-01-01

A historical sketch of the activity of Romanian Rare Metals Enterprises is presented stressing the valorization of rare metals like: - radioactive metals, uranium and thorium; - dispersed rare metals, molybdenum, monazite; - heavy and refractory metals, titanium and zirconium; rare earths, lanthanides and yttrics. The beginning and developing of research in the nuclear field is in closed relation to the existence on the domestic territory of important uranium ores the mining of which begun early in 1954. The exploitation of Baita-Bihor orebody was followed by that at Ciudanovita, Natra and Dobrei ores in Caras-Severin county. Concomitantly with the ore mining, geological research was developed covering vast areas of country's surface and using advanced investigation tools suitable for increasing depths. The next step in the nuclear fuel program was made by building a uranium concentrate (as ammonium or sodium diuranate) plant. Two purification units for processing the uranium concentrate to sintered uranium dioxide powder were completed and commissioned at Feldioara in 1986. The quality of the uranium dioxide product meets the quality standards requirements for CANDU type nuclear fuel as certified in 1994. Currently, part of the fuel load of Cernavoda reactor is fuel element clusters produced by Nuclear Fuel Plant at Pitesti of sintered powder processed at Feldioara. A list of strategic objectives of the Uranium National Company is presented among which: - maintaining the uranium mining and milling activities in close relation with the fuel requirements of Cernavoda NPP; continuing geological research in promising zones, to find new uranium orebodies, easy to mill cost effectively; decreasing the environmental impact in the geological research areas, in mining and transport affected areas and in the processing plants. The fuel demand of current operation of Cernavoda NPP Unit 1 as well as of future Unit 2 after commissioning are and will be satisfied by the

Development of high uranium-density fuels for use in research reactors

Energy Technology Data Exchange (ETDEWEB)

Ugajin, Mitsuhiro; Akabori, Mitsuo; Itoh, Akinori [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

1996-02-01

The uranium silicide U{sub 3}Si{sub 2} possesses uranium density 11.3 gU/cm{sup 3} with a congruent melting point of 1665degC, and is now successfully in use as a research reactor fuel. Another uranium silicide U{sub 3}Si and U{sub 6}Me-type uranium alloys (Me=Fe,Mn,Ni) have been chosen as new fuel materials because of the higher uranium densities 14.9 and 17.0 gU/cm{sup 3}, respectively. Experiments were carried out to fabricate miniature aluminum-dispersion plate-type and aluminum-clad disk-type fuels by using the conventional picture-frame method and a hot-pressing technique, respectively. These included the above-mentioned new fuel materials as well as U{sub 3}Si{sub 2}. Totally 14 miniplates with uranium densities from 4.0 to 6.3 gU/cm{sup 3} of fuel meat were prepared together with 28 disk-type fuel containing structurally-modified U{sub 3}Si, and subjected to the neutron irradiation in JMTR (Japan Materials Testing Reactor). Some results of postirradiation examinations are presented. (author)

Improvement of cesium retention in uranium dioxide by additional phases

International Nuclear Information System (INIS)

Gamaury Dubois, S.

1995-01-01

The objective of this study is to improve the cesium retention in nuclear fuel. A bibliographic survey indicates that cesium is rapidly released from uranium dioxide in an accident condition. At temperatures higher than 1500 deg C or in oxidising conditions, our experiments show the difficulty of maintaining cesium inside simulated fuel. Two ternary systems are potentially interesting for the retention of cesium and to reduce the kinetics of release from the fuel: Cs 2 O-Al 2 O 3 -SiO 2 et Cs 2 O-ZrO 2 -SO 2 . The compounds CsAISi 2 O 6 and Cs 2 ZrSi 6 O 15 were studied from 1200 deg C to 2000 deg C by thermogravimetric analysis. The volumetric diffusion coefficients of cesium in these structures, in solid state as well as in liquid one, were measured. A fuel was sintered with (Al 2 O 3 + SiO 2 ) or (ZrO 2 + SiO 2 ) and the intergranular phase was characterized. In the presence of (Al 2 O 3 + SiO 2 ), the sintering is realized at 1610 deg C in H 2 . It is a liquid phase sintering. On the other end, with (ZrO 2 + SiO 2 ), the sintering is a low temperature one in oxidising atmosphere. Finally, cesium containing simulated fuels were produced with these additives. According to the effective diffusion coefficients that were measured, the additives improved the retention of cesium. We have predicted the improvement that could be hoped for in a nuclear reactor, depending on the dispersion of the intergranular additives, the temperature and the degree of oxidation of the UO 2+x . We wait for a factor of 2 for x=0 and more than 8 for x=0.05, up to 2000 deg C. (author). 148 refs., 122 figs., 34 tabs

Uranium for Nuclear Power: Resources, Mining and Transformation to Fuel

International Nuclear Information System (INIS)

Hore-Lacy, Ian

2016-01-01

Uranium for Nuclear Power: Resources, Mining and Transformation to Fuel discusses the nuclear industry and its dependence on a steady supply of competitively priced uranium as a key factor in its long-term sustainability. A better understanding of uranium ore geology and advances in exploration and mining methods will facilitate the discovery and exploitation of new uranium deposits. The practice of efficient, safe, environmentally-benign exploration, mining and milling technologies, and effective site decommissioning and remediation are also fundamental to the public image of nuclear power. This book provides a comprehensive review of developments in these areas: • Provides researchers in academia and industry with an authoritative overview of the front end of the nuclear fuel cycle • Presents a comprehensive and systematic coverage of geology, mining, and conversion to fuel, alternative fuel sources, and the environmental and social aspects • Written by leading experts in the field of nuclear power, uranium mining, milling, and geological exploration who highlight the best practices needed to ensure environmental safety

The low enriched uranium fuel cycle in Ontario

International Nuclear Information System (INIS)

Archinoff, G.H.

1979-02-01

Six fuel-cycle strategies for use in CANDU reactors are examined in terms of their uranium-conserving properties and their ease of commercialization for three assumed growth rates of installed nuclear capacity in Ontario. The fuel cycle strategies considered assume the continued use of the natural uranium cycle up to the mid-1990's. At that time, the low-enriched uranium (LEU) cycle is gradually introduced into the existing power generation grid. In the mid-2020's one of four advanced cycles is introduced. The advanced cycles considered are: mixed oxide, intermediate burn-up thorium (Pu topping), intermediate burn-up thorium (U topping), and LMFBR. For comparison purposes an all natural uranium strategy and a natural uranium-LEU strategy (with no advanced cycle) are also included. None of the strategies emerges as a clear, overall best choice. (LL)

Methods for oxygen/uranium ratio determination in substoichiometric uranium dioxide

International Nuclear Information System (INIS)

Baranov, V.G.; Godin, Yu.G.; S'edin, Yu.D.; Kosykh, V.G.; Nepryakhin, A.M.; Komarenko, F.F.; Kutyreva, G.A.

1994-01-01

Investigations are performed into a possibility to use the methods of thermal gravimetric analysis, gas chromatography, hydration-dehydration, and e.m.f. of high-temperature solid-electrode galvanic cell for determining O-U atomic ratio in UO 2-x . It is shown that the investigated methods have an analysis error of ± 0.001 O/U units. However, the e.m.f. method, which feature a high accuracy near stoichiometry can be applied only within the limits of UO 2-x homogeneity. A possibility is shown to expend the area of e.m.f. method application during the analysis of substoichiometric uranium dioxide. 9 refs.; 1 tab

Irradiation behavior of miniature experimental uranium silicide fuel plates

International Nuclear Information System (INIS)

Hofman, G.L.; Neimark, L.A.; Mattas, R.F.

1983-01-01

Uranium silicides, because of their relatively high uranium density, were selected as candidate dispersion fuels for the higher fuel densities required in the Reduced Enrichment Research and Test Reactor (RERTR) Program. Irradiation experience with this type of fuel, however, was limited to relatively modest fission densities in the bulk from, on the order of 7 x 10 20 cm -3 , far short of the approximately 20 x 10 20 cm -3 goal established for the RERTR program. The purpose of the irradiation experiments on silicide fuels on the ORR, therefore, was to investigate the intrinsic irradiation behavior of uranium silicide as a dispersion fuel. Of particular interest was the interaction between the silicide particles and the aluminum matrix, the swelling behavior of the silicide particles, and the maximum volume fraction of silicide particles that could be contained in the aluminum matrix

High temperature behavior of metallic inclusions in uranium dioxide

International Nuclear Information System (INIS)

Yang, R.L.

1980-08-01

The object of this thesis was to construct a temperature gradient furnace to simulate the thermal conditions in the reactor fuel and to study the migration of metallic inclusions in uranium oxide under the influence of temperature gradient. No thermal migration of molybdenum and tungsten inclusions was observed under the experimental conditions. Ruthenium inclusions, however, dissolved and diffused atomically through grain boundaries in slightly reduced uranium oxide. An intermetallic compound (probably URu 3 ) was formed by reaction of Ru and UO/sub 2-x/. The diffusivity and solubility of ruthenium in uranium oxide were measured

Recovery and recycling of uranium from rejected coated particles for compact high temperature reactors

Energy Technology Data Exchange (ETDEWEB)

Pai, Rajesh V., E-mail: pairajesh007@gmail.com [Fuel Chemistry Division, Bhabha Atomic Research Centre, Mumbai (India); Mollick, P.K. [Powder Metallurgy Division, Bhabha Atomic Research Centre, Mumbai (India); Kumar, Ashok [Fuel Chemistry Division, Bhabha Atomic Research Centre, Mumbai (India); Banerjee, J. [Radiometullurgy Division, Bhabha Atomic Research Centre, Mumbai (India); Radhakrishna, J. [Fuel Chemistry Division, Bhabha Atomic Research Centre, Mumbai (India); Chakravartty, J.K. [Powder Metallurgy Division, Bhabha Atomic Research Centre, Mumbai (India)

2016-05-15

UO{sub 2} microspheres prepared by internal gelation technique were coated with pyrolytic carbon and silicon carbide using CVD technique. The particles which were not meeting the specifications were rejected. The rejected/failed UO{sub 2} based coated particles prepared by CVD technique was used for oxidation and recovery and recycling. The oxidation behaviour of sintered UO{sub 2} microspheres coated with different layers of carbon and SiC was studied by thermal techniques to develop a method for recycling and recovery of uranium from the failed/rejected coated particles. It was observed that the complete removal of outer carbon from the spheres is difficult. The crushing of microspheres enabled easier accessibility of oxygen and oxidation of carbon and uranium at 800–1000 °C. With the optimized process of multiple crushing using die & plunger and sieving the broken coated layers, we could recycle around fifty percent of the UO{sub 2} microspheres which could be directly recoated. The rest of the particles were recycled using a wet recycling method. - Highlights: • The oxidation behaviour of coated particles was studied in air, O{sub 2} and moist O{sub 2}. • It was observed that coated layers cannot be completely removed by mere oxidation. • Complete recovery of uranium from the rejected coated particles has been carried out using a combination of dry and wet recovery scheme. • A crushing step prior to oxidation is needed for full recovery of uranium from the coated particles.

Transition from uranium to denatured uranium/thorium fuel in an existing PWR

International Nuclear Information System (INIS)

Walters, M.A.

1982-01-01

The purpose of this research was to determine whether it is possible to make a gradual transition from uranium to denatured uranium/thorium (DUTH) fuel in an existing PWR by adding DUTH assemblies during each scheduled refueling and, if the transition is possible, to develop a general procedure for making it. The feasibility of the transition was established by identifying acceptable refueling schemes for a series of transition cores, and in the process, a method for identifying acceptable schemes evolved. The utility of the method was then demonstrated by applying it to a standard reactor operating under normal conditions. The vehicle used to examine proposed fuel mixtures and to select acceptable ones was a set of one-dimensional computer codes. The core was modeled as a set of five concentric fuel zones with a reflector. Fuel mixtures were proposed and the computer codes were used to determine whether a mixture was acceptable, i.e., whether it had the desired k-effective and flux and power distributions. The parameters allowed to vary in selection of proposed fuel mixtures were enrichment of fresh fuel assemblies, number of uranium and DUTH assemblies added during each refueling, and distribution of fuel in the core. Results of the research showed that a gradual transition is possible. Furthermore, there is a method that allows the identification of fuel mixtures that are likely to be acceptable. It requires the calculation of K-infinity for the entire proposed core and for some of its regions. These values of K-infinity and relationships developed in this research can be used to predict the flux distribution and the final k-effective for the proposed fuel mixture

ELECTROCHEMICAL STUDIES OF URANIUM METAL CORROSION MECHANISM AND KINETICS IN WATER

International Nuclear Information System (INIS)

Boudanova, Natalya; Maslennikov, Alexander; Peretroukhine, Vladimir F.; Delegard, Calvin H.

2006-01-01

During long-term underwater storage of low burn-up uranium metal fuel, a corrosion product sludge forms containing uranium metal grains, uranium dioxide, uranates and, in some cases, uranium peroxide. Literature data on the corrosion of non-irradiated uranium metal and its alloys do not allow unequivocal prediction of the paragenesis of irradiated uranium in water. The goal of the present work conducted under the program 'CORROSION OF IRRADIATED URANIUM ALLOYS FUEL IN WATER' is to study the corrosion of uranium and uranium alloys and the paragenesis of the corrosion products during long-term underwater storage of uranium alloy fuel irradiated at the Hanford Site. The elucidation of the physico-chemical nature of the corrosion of irradiated uranium alloys in comparison with non-irradiated uranium metal and its alloys is one of the most important aspects of this work. Electrochemical methods are being used to study uranium metal corrosion mechanism and kinetics. The present part of work aims to examine and revise, where appropriate, the understanding of uranium metal corrosion mechanism and kinetics in water

Micromechanical simulation of Uranium dioxide polycrystalline aggregate behaviour under irradiation

International Nuclear Information System (INIS)

Pacull, J.

2011-02-01

In pressurized water nuclear power reactor (PWR), the fuel rod is made of dioxide of uranium (UO 2 ) pellet stacked in a metallic cladding. A multi scale and multi-physic approaches are needed for the simulation of fuel behavior under irradiation. The main phenomena to take into account are thermomechanical behavior of the fuel rod and chemical-physic behavior of the fission products. These last years one of the scientific issue to improve the simulation is to take into account the multi-physic coupling problem at the microscopic scale. The objective of this ph-D study is to contribute to this multi-scale approach. The present work concerns the micro-mechanical behavior of a polycrystalline aggregate of UO 2 . Mean field and full field approaches are considered. For the former and the later a self consistent homogenization technique and a periodic Finite Element model base on the 3D Voronoi pattern are respectively used. Fuel visco-plasticity is introduced in the model at the scale of a single grain by taking into account specific dislocation slip systems of UO 2 . A cohesive zone model has also been developed and implemented to simulate grain boundary sliding and intergranular crack opening. The effective homogenous behaviour of a Representative Volume Element (RVE) is fitted with experimental data coming from mechanical tests on a single pellet. Local behavior is also analyzed in order to evaluate the model capacity to assess micro-mechanical state. In particular, intra and inter granular stress gradient are discussed. A first validation of the local behavior assessment is proposed through the simulation of intergranular crack opening measured in a compressive creep test of a single fuel pellet. Concerning the impact of the microstructure on the fuel behavior under irradiation, a RVE simulation with a representative transient loading of a fuel rod during a power ramp test is achieved. The impact of local stress and strain heterogeneities on the multi

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.

Surface characterisation and electrochemical behaviour of porous titanium dioxide coated 316L stainless steel for orthopaedic applications

International Nuclear Information System (INIS)

Nagarajan, S.; Rajendran, N.

2009-01-01

Porous titanium dioxide was coated on surgical grade 316L stainless steel (SS) and its role on the corrosion protection and enhanced biocompatibility of the materials was studied. X-ray diffraction analysis (XRD), atomic force microscopy (AFM), Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy (SEM) and energy dispersive X-ray analysis (EDAX) were carried out to characterise the surface morphology and also to understand the structure of the as synthesised coating on the substrates. The corrosion behaviour of titanium dioxide coated samples in simulated body fluid was evaluated using polarisation and impedance spectroscopy studies. The results reveal that the titanium dioxide coated 316L SS exhibit a higher corrosion resistance than the uncoated 316L SS. The titanium dioxide coated surface is porous, uniform and also it acts as a barrier layer to metallic substrate and the porous titanium dioxide coating induces the formation of hydroxyapatite layer on the metal surface.

Carbon dioxide from fossil fuels: adapting to uncertainty

Energy Technology Data Exchange (ETDEWEB)

Chen, K; Winter, R C; Bergman, M K

1980-12-01

If present scientific information is reasonable, the world is likely to experience noticeable global warming by the beginning of the next century if high annual growth rates of fossil-fuel energy use continue. Only with optimistic assumptions and low growth rates will carbon-dioxide-induced temperature increases be held below 2/sup 0/C or so over the next century. Conservation, flexible energy choices, and control options could lessen the potential effects of carbon dioxide. Though perhaps impractical from the standpoint of costs and efficiency losses, large coastal centralized facilities would be the most amenable to carbon dioxide control and disposal. Yet no country can control carbon dioxide levels unilaterally. The USA, however, which currently contributes over a quarter of all fossil-fuel carbon dioxide emissions and possesses a quarter of the world's coal resources, could provide a much needed role in leadership, research and education. 70 references.

Sensitivity study for accident tolerant fuels: Property comparisons and behavior simulations in a simplified PWR to enable ATF development and design

Energy Technology Data Exchange (ETDEWEB)

Spencer, Kristina Yancey, E-mail: kristina.yancey@gmail.com; Sudderth, Laura; Brito, Ryan A.; Evans, Jordan A.; Hart, Clifford S.; Hu, Anbang; Jati, Andi; Stern, Karyn; McDeavitt, Sean M., E-mail: mcdeavitt@tamu.edu

2016-12-01

Highlights: • This study compared four accident tolerant fuels against uranium dioxide. • Material property correlations were developed to evaluate fuel performance. • The fuels’ neutronic and thermal hydraulic behaviors were studied in the AP1000. • No fuel type performed better in all areas, but each has strengths and weaknesses. • More research is needed to build a complete model of the fuel performances. - Abstract: Since the events at the Fukushima-Daiichi nuclear power plant, there has been increased interest in developing fuels to better withstand accidents for current light water reactors. Four accident tolerant fuel candidates are uranium oxide with beryllium oxide additives, uranium oxide with silicon carbide matrix additives, uranium nitride, and uranium nitride with uranium silicide composite. The first two candidates represent near-term high performance uranium oxide with high thermal conductivity and neutron transparency, and the second two represent mid-term high-density fuels with highly beneficial thermal properties. This study seeks to understand the benefits and drawbacks of each option in place of uranium dioxide. To assess the material properties for each of the fuel types, an extensive literature review was performed for material property data. Correlations were then made to evaluate the properties during reactor operation. Neutronics and thermal hydraulics studies were also completed to determine the impact of the use of each candidate in an AP1000 reactor. In most cases, the candidate fuels performed more desirably than uranium dioxide, but no fuel type performed better in all aspects. Much more research needs to be performed to build a complete model of the fuel performances, primarily experimental data for uranium silicide. Each of the fuels studied has its own benefits and drawbacks, and the comparisons discussed in this report can be used to aid in determining the most appropriate fuel depending on the desired specifications.

Choice and utilization of slightly enriched uranium fuel for high performance research reactors

International Nuclear Information System (INIS)

Cerles, J.M.; Schwartz, J.P.

1978-01-01

Problems relating to the replacement of highly enriched (90% or 93% U 235 ) uranium fuel: by moderately enriched (20% or 40% in U 235 ) metallic uranium fuel and slightly enriched (3% or 8% in U 235 ) uranium oxide fuel are discussed

Characterisation of electrodeposited polycrystalline uranium dioxide thin films on nickel foil for industrial applications

International Nuclear Information System (INIS)

Adamska, A.M.; Bright, E. Lawrence; Sutcliffe, J.; Liu, W.; Payton, O.D.; Picco, L.; Scott, T.B.

2015-01-01

Polycrystalline uranium dioxide thin films were grown on nickel substrates via aqueous electrodeposition of a precursor uranyl salt. The arising semiconducting uranium dioxide thin films exhibited a tower-like morphology, which may be suitable for future application in 3D solar cell applications. The thickness of the homogenous, tower-like films reached 350 nm. Longer deposition times led to the formation of thicker (up to 1.5 μm) and highly porous films. - Highlights: • Electrodeposition of polycrystalline UO_2 thin films • Tower-like morphology for 3D solar cell applications • Novel technique for separation of heavy elements from radioactive waste streams

Method of manufacturing a graphite coated fuel can

International Nuclear Information System (INIS)

Saito, Koichi; Uchida, Shunsuke.

1984-01-01

Purpose: To improve the close bondability and homogeneity of a graphite coating formed at the inner surface of a fuel can. Method: A coating containing graphite dispersed in a volatile organic solvent is used and a graphite coating is formed to the inner surface of a fuel can by way of a plunger method. After applying graphite coating, an inert gas is caused to flow at a certain flow rate to the inside of the fuel can horizontally rotaged so that gassification and evaporation of the volatile organic solvent contained in the graphite coating may be promoted. Since drying of the graphite coating coated to the inner surface of the fuel can thus be controlled, a graphite coating with satisfactory close bondability and homogeneity can be formed. (Kawakami, Y.)

Fabrication of fuel elements on the basis of increased concentration fuel composition

International Nuclear Information System (INIS)

Alexandrov, A.B.; Afanasiev, V.L.; Enin, A.A.; Suprun, V.B.

2004-01-01

As a part of Russian Program RERTR Reduced Enrichment for Research and Test Reactors), at NCCP, Inc. jointly with the State Scientific Centre VNIINM the mastering in industrial environment of design and fabrication process of fuel elements (FE) with increased concentration fuel compositions is performed. Fuel elements with fuel composition on the basis of dioxide uranium with nearly 4 g/cm 3 fuel concentration have been produced thus confirming the principal possibility of fuel enrichment reduction down to 20% for research reactors which were built up according to the projects of the former USSR, by increasing the oxide fuel concentration in fuel assemblies (FAs). The form and geometrical dimensions of FEs and FAs shall remain unchanged, only uranium mass in FA shall be increased. (author)

Linking fuel design features ampersand plant management to uranium, SWU savings

International Nuclear Information System (INIS)

Anon.

1992-01-01

This article, contributed by Scott Garrett, Manager of Planning and Uranium Operations for Siemens Power Corporation in Bellevue, Washington, explores the impact of advances in fuel design and fuel management strategies on uranium utilization in the United States. Nuclear plant operators are deriving substantial benefits from these changes, including longer fuel cycle lengths, increased burnup, and added capacity - and experiencing cost savings in both uranium and enrichment services at the same time

Literature review of thermal and radiation performance parameters for high-temperature, uranium dioxide fueled cermet materials

International Nuclear Information System (INIS)

Haertling, C.; Hanrahan, R.J.

2007-01-01

High-temperature fissile-fueled cermet literature was reviewed. Data are presented primarily for the W-UO 2 as this was the system most frequently studied; other reviewed systems include cermets with Mo, Re, or alloys as a matrix. Failure mechanisms for the cermets are typically degradation of mechanical integrity and loss of fuel. Mechanical failure can occur through stresses produced from dissimilar expansion coefficients, voids created from diffusion of dissimilar materials or formation of metal hydride and subsequent volume expansion. Fuel loss failure can occur by high temperature surface vaporization or by vaporization after loss of mechanical integrity. Techniques found to aid in retaining fuel include the use of coatings around UO 2 fuel particles, use of oxide stabilizers in the UO 2 , minimizing grain sizes in the metal matrix, minimizing impurities, controlling the cermet sintering atmosphere, and cladding around the cermet

Experiments of JRR-4 low-enriched-uranium-silicied fuel core

International Nuclear Information System (INIS)

Hirane, Nobuhiko; Ishikuro, Yasuhiro; Nagadomi, Hideki; Yokoo, Kenji; Horiguchi, Hironori; Nemoto, Takumi; Yamamoto, Kazuyoshi; Yagi, Masahiro; Arai, Nobuyoshi; Watanabe, Shukichi; Kashima, Yoichi

2006-03-01

JRR-4, a light-water-moderated and cooled, swimming pool type research reactor using high-enriched uranium plate-type fuels had been operated from 1965 to 1996. In order to convert to low-enriched-uranium-silicied fuels, modification work had been carried out for 2 years, from 1996 to 1998. After the modification, start-up experiments were carried out to obtain characteristics of the low-enriched-uranium-silicied fuel core. The measured excess reactivity, reactor shutdown margin and the maximum reactivity addition rate satisfied the nuclear limitation of the safety report for licensing. It was confirmed that conversion to low-enriched-uranium-silicied fuels was carried out properly. Besides, the necessary data for reactor operation were obtained, such as nuclear, thermal hydraulic and reactor control characteristics. This report describes the results of start-up experiments and burnup experiments. The first criticality of low-enriched-uranium-silicied core was achieved on 14th July 1998, and the operation for joint-use has been carried out since 6th October 1998. (author)

Physicochemical analysis of interaction of oxide fuel with pyrocarbon coatings of fuel particles

International Nuclear Information System (INIS)

Lyutikov, R.A.; Khromov, Yu.F.; Chernikov, A.S.

1990-01-01

Equilibrium pressure of (CO+Kr,Xe) gases inside fuel particle with oxide kern depending on design features of fuel particle, on temperature. on (O/U) initial composition and fuel burnup is calculated using the suggested model. Analysis of possibility for gas pressure reduction by means of uranium carbide alloying of kern and degree increase of solid fission product retention (Cs for example) during alumosilicate alloying of uranium oxide is conducted

Depleted uranium oxides as spent-nuclear-fuel waste-package fill materials

International Nuclear Information System (INIS)

Forsberg, C.W.

1997-01-01

Depleted uranium dioxide fill inside the waste package creates the potential for significant improvements in package performance based on uranium geochemistry, reduces the potential for criticality in a repository, and consumes DU inventory. As a new concept, significant uncertainties exist: fill properties, impacts on package design, post- closure performance

Comparison of the radiological impacts of thorium and uranium nuclear fuel cycles

International Nuclear Information System (INIS)

Meyer, H.R.; Witherspoon, J.P.; McBride, J.P.; Frederick, E.J.

1982-03-01

This report compares the radiological impacts of a fuel cycle in which only uranium is recycled, as presented in the Final Generic Environmental Statement on the Use of Recycle Plutonium in Mixed Oxide Fuel in Light Water Cooled Reactors (GESMO), with those of the light-water breeder reactor (LWBR) thorium/uranium fuel cycle in the Final Environmental Statement, Light Water Breeder Reactor Program. The significant offsite radiological impacts from routine operation of the fuel cycles result from the mining and milling of thorium and uranium ores, reprocessing spent fuel, and reactor operations. The major difference between the impacts from the two fuel cycles is the larger dose commitments associated with current uranium mining and milling operations as compared to thorium mining and milling. Estimated dose commitments from the reprocessing of either fuel type are small and show only moderate variations for specific doses. No significant differences in environmental radiological impact are anticipated for reactors using either of the fuel cycles. Radiological impacts associated with routine releases from the operation of either the thorium or uranium fuel cycles can be held to acceptably low levels by existing regulations

WWER-1000 nuclear fuel manufacturing process at PJSC MSZ

International Nuclear Information System (INIS)

Morylev, A.; Bagdatyeva, E.; Aksenov, P.

2015-01-01

In this report a brief description of WWER-1000 fuel manufacturing process steps at PJSC MSZ as: uranium dioxide powder fabrication; fuel pellet manufacture fuel rod manufacture working assembly and fuel assembly manufacture is given. The implemented innovations are also presented

Study of process parameters for reducing ammonium uranyl carbonate to uranium dioxide in fluidized bed furnace

International Nuclear Information System (INIS)

Leitao Junior, C.B.

1992-01-01

This work consists of studying the process parameters of AUC (ammonium uranyl carbonate) to U O 2 (uranium dioxide) reduction, with good physical and chemical characteristics, in fluidized bed. Initially, it was performed U O 2 cold fluidization experiments with an acrylic column. Afterward, it was done AUC to U O 2 reduction experiments, in which the process parameters influence in the granulometry, specific surface area, porosity and fluoride amount on the U O 2 powder produced were studied. As a last step, it was done compacting and sintering tests of U O 2 pellets in order to appreciate the U O 2 powder performance, obtained by fluidized bed, in the fuel pellets fabrication. (author)

Once-through uranium thorium fuel cycle in CANDU reactors

International Nuclear Information System (INIS)

Ozdemir, S.; Cubukcu, E.

2000-01-01

In this study, the performance of the once-through uranium-thorium fuel cycle in CANDU reactors is investigated. (Th-U)O 2 is used as fuel in all fuel rod clusters where Th and U are mixed homogeneously. CANDU reactors have the advantage of being capable of employing various fuel cycle options because of its good neutron economy, continuous on line refueling ability and axial fuel replacement possibility. For lattice cell calculations transport code WIMS is used. WIMS cross-section library is modified to achieve precise lattice cell calculations. For various enrichments and Th-U mixtures, criticality, heavy element composition changes, diffusion coefficients and cross-sections are calculate. Reactor core is modeled by using the diffusion code CITATION. We conclude that an overall saving of 22% in natural uranium demand can be achieved with the use of Th cycle. However, slightly enriched U cycle still consumes less natural Uranium and is a lot less complicated. (author)

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)

The nuclear fuel cycle, From the uranium mine to waste disposal

International Nuclear Information System (INIS)

2002-09-01

Fuel is a material that can be burnt to provide heat. The most familiar fuels are wood, coal, natural gas and oil. By analogy, the uranium used in nuclear power plants is called 'nuclear fuel', because it gives off heat too, although, in this case, the heat is obtained through fission and not combustion. After being used in the reactor, spent nuclear fuel can be reprocessed to extract recyclable energy material, which is why we speak of the nuclear fuel cycle. This cycle includes all the following industrial operations: - uranium mining, - fuel fabrication, - use in the reactor, - reprocessing the fuel unloaded from the reactor, - waste treatment and disposal. 'The nuclear fuel cycle includes an array of industrial operations, from uranium mining to the disposal of radioactive waste'. Per unit or mass (e.g. per kilo), nuclear fuel supplies far more energy than a fossil fuel (coal or oil). When used in a pressurised water reactor, a kilo of uranium generates 10,000 times more energy than a kilo of coal or oil in a conventional power station. Also, the fuel will remain in the reactor for a long time (several years), unlike conventional fuels, which are burnt up quickly. Nuclear fuel also differs from others in that uranium has to undergo many processes between the time it is mined and the time it goes into the reactor. For the sake of simplicity, the following pages will only look at nuclear fuel used in pressurised water reactors (or PWRs), because nuclear power plants consisting of one or more PWRs are the most widely used around the world. (authors)

A spectroscopic study of uranium species formed in chloride melts

International Nuclear Information System (INIS)

Volkovich, Vladimir A.; Bhatt, Anand I.; May, Iain; Griffiths, Trevor R.; Thied, Robert C.

2002-01-01

The chlorination of uranium metal or uranium oxides in chloride melts offers an acceptable process for the head-end of pyrochemical reprocessing of spent nuclear fuels. The reactions of uranium metal and ceramic uranium dioxide with chlorine and with hydrogen chloride were studied in the alkali metal chloride melts, NaCl-KCl at 973K, NaCl-CsCl between 873 and 923K and LiCl-KCl at 873K. The uranium species formed therein were characterized from their electronic absorption spectra measured in situ. The kinetic parameters of the reactions depend on melt composition, temperature and chlorinating agent used. The reaction of uranium dioxide with oxygen in the presence of alkali metal chlorides results in the formation of alkali metal uranates. A spectroscopic study, between 723 and 973K, on their formation and their solutions was undertaken in LiCl, LiCl-KCl eutectic and NaCl-CsCl eutectic melts. The dissolution of uranium dioxide in LiCl-KCl eutectic at 923K containing added aluminium trichloride in the presence of oxygen has also been investigated. In this case, the reaction leads to the formation of uranyl chloride species. (author)

Uranium Oxide Rate Summary for the Spent Nuclear Fuel (SNF) Project (OCRWM)

Energy Technology Data Exchange (ETDEWEB)

PAJUNEN, A.L.

2000-09-20

The purpose of this document is to summarize the uranium oxidation reaction rate information developed by the Hanford Spent Nuclear Fuel (SNF) Project and describe the basis for selecting reaction rate correlations used in system design. The selection basis considers the conditions of practical interest to the fuel removal processes and the reaction rate application during design studies. Since the reaction rate correlations are potentially used over a range of conditions, depending of the type of evaluation being performed, a method for transitioning between oxidation reactions is also documented. The document scope is limited to uranium oxidation reactions of primary interest to the SNF Project processes. The reactions influencing fuel removal processes, and supporting accident analyses, are: uranium-water vapor, uranium-liquid water, uranium-moist air, and uranium-dry air. The correlation selection basis will consider input from all available sources that indicate the oxidation rate of uranium fuel, including the literature data, confirmatory experimental studies, and fuel element observations. Trimble (2000) summarizes literature data and the results of laboratory scale experimental studies. This document combines the information in Trimble (2000) with larger scale reaction observations to describe uranium oxidation rate correlations applicable to conditions of interest to the SNF Project.

Uranium Oxide Rate Summary for the Spent Nuclear Fuel (SNF) Project (OCRWM)

International Nuclear Information System (INIS)

PAJUNEN, A.L.

2000-01-01

The purpose of this document is to summarize the uranium oxidation reaction rate information developed by the Hanford Spent Nuclear Fuel (SNF) Project and describe the basis for selecting reaction rate correlations used in system design. The selection basis considers the conditions of practical interest to the fuel removal processes and the reaction rate application during design studies. Since the reaction rate correlations are potentially used over a range of conditions, depending of the type of evaluation being performed, a method for transitioning between oxidation reactions is also documented. The document scope is limited to uranium oxidation reactions of primary interest to the SNF Project processes. The reactions influencing fuel removal processes, and supporting accident analyses, are: uranium-water vapor, uranium-liquid water, uranium-moist air, and uranium-dry air. The correlation selection basis will consider input from all available sources that indicate the oxidation rate of uranium fuel, including the literature data, confirmatory experimental studies, and fuel element observations. Trimble (2000) summarizes literature data and the results of laboratory scale experimental studies. This document combines the information in Trimble (2000) with larger scale reaction observations to describe uranium oxidation rate correlations applicable to conditions of interest to the SNF Project

Development of very-high-density low-enriched-uranium fuels

International Nuclear Information System (INIS)

Snelgrove, J.L.; Hofman, G.L.; Meyer, M.K.; Trybus, C.L.; Wiencek, T.C.

1997-01-01

Following a hiatus of several years and following its successful development and qualification of 4.8 g U cm -3 U 3 Si 2 -Al dispersion fuel for application with low-enriched uranium in research and test reactors, the US Reduced Enrichment for Research and Test Reactors program has embarked on the development of even-higher-density fuels. Our goal is to achieve uranium densities of 8-9 g cm -3 in aluminum-based dispersion fuels. Achieving this goal will require the use of high-density, γ-stabilized uranium alloy powders in conjunction with the most-advanced fuel fabrication techniques. Key issues being addressed are the reaction of the fuel alloys with aluminum and the irradiation behavior of the fuel alloys and any reaction products. Test irradiations of candidate fuels in very-small (micro) plates are scheduled to begin in the Advanced Test Reactor during June, 1997. Initial results are expected to be available in early 1998. We are performing out-of-reactor studies on the phase structure of the candidate alloys on diffusion of the matrix material into the aluminum. In addition, we are modifying our current dispersion fuel irradiation behavior model to accommodate the new fuels. Several international partners are participating in various phases of this work. (orig.)

Experience with a uranyl nitrate/uranium dioxide conversion pilot plant

International Nuclear Information System (INIS)

Arcuri, L.; Pietrelli, L.

1984-01-01

A plant for the precipitation of sinterable nuclear grade UO 2 powders is described in this report. The plant has been designed, built and set up by SNIA TECHINT. ENEA has been involved in the job as nuclear consultant. Main process steps are: dissolution of UO 2 powder or sintered UO 2 pellets, adjustment of uranyl nitrate solutions, precipitation of uranium peroxide by means of hydrogen peroxide, centrifugation of the precipitate, drying, calcination and reduction to uranium dioxide. The report is divided in two main section: the process description and the ''hot test'' report. Some laboratory data on precipitation of ammonium diuranate by means of NH 4 OH, are also reported

Irradiation behavior of uranium-molybdenum dispersion fuel: Fuel performance data from RERTR-1 and RERTR-2

International Nuclear Information System (INIS)

Meyer, M.K.; Clark, C.R.; Hayes, S.L.; Strain, R.V.; Hofman, G.L.; Snelgrove, J.L.; Park, J.M.; Kim, K.H.

1999-01-01

This paper presents quantitative data on the irradiation behavior of uranium-molybdenum fuels from the low temperature RERTR-1 and -2 experiments. Fuel swelling measurements of U-Mo fuels at ∼40% and ∼70% burnup are presented. The rate of fuel-matrix interaction layer growth is estimated. Microstructures of fuel in the pre- and postirradiation condition were compared. Based on these data, a qualitative picture of the evolution of the U-Mo fuel microstructure during irradiation has been developed. Estimates of uranium-molybdenum fuel swelling and fuel-matrix interaction under high-power research reactor operating conditions are presented. (author)

Uranium plutonium oxide fuels

International Nuclear Information System (INIS)

Cox, C.M.; Leggett, R.D.; Weber, E.T.

1981-01-01

Uranium plutonium oxide is the principal fuel material for liquid metal fast breeder reactors (LMFBR's) throughout the world. Development of this material has been a reasonably straightforward evolution from the UO 2 used routinely in the light water reactor (LWR's); but, because of the lower neutron capture cross sections and much lower coolant pressures in the sodium cooled LMFBR's, the fuel is operated to much higher discharge exposures than that of a LWR. A typical LMFBR fuel assembly is shown. Depending on the required power output and the configuration of the reactor, some 70 to 400 such fuel assemblies are clustered to form the core. There is a wide variation in cross section and length of the assemblies where the increasing size reflects a chronological increase in plant size and power output as well as considerations of decreasing the net fuel cycle cost. Design and performance characteristics are described

Preparation of UC0.07-0.10N0.90-0.93 spheres for TRISO coated fuel particles

Science.gov (United States)

Hunt, R. D.; Silva, C. M.; Lindemer, T. B.; Johnson, J. A.; Collins, J. L.

2014-05-01

The US Department of Energy is considering a new nuclear fuel that would be less susceptible to ruptures during a loss-of-coolant accident. The fuel would consist of tristructural isotropic coated particles with dense uranium nitride (UN) kernels with diameters of 650 or 800 μm. The objectives of this effort are to make uranium oxide microspheres with adequately dispersed carbon nanoparticles and to convert these microspheres into UN spheres, which could be then sintered into kernels. Recent improvements to the internal gelation process were successfully applied to the production of uranium gel spheres with different concentrations of carbon black. After the spheres were washed and dried, a simple two-step heat profile was used to produce porous microspheres with a chemical composition of UC0.07-0.10N0.90-0.93. The first step involved heating the microspheres to 2023 K in a vacuum, and in the second step, the microspheres were held at 1873 K for 6 h in flowing nitrogen.

Nuclear fuel recycling system

International Nuclear Information System (INIS)

Lee, H.R.; Koch, A.K.; Krawczyk, A.

1981-01-01

A process is provided for recycling sintered uranium dioxide fuel pellets rejected during fuel manufacture and the swarf from pellet grinding. The scrap material is prepared mechanically by crushing and milling as a high solids content slurry, using scrap sintered UO 2 pellets as the grinding medium under an inert atmosophere

Irradiation performance of uranium-molybdenum alloy dispersion fuels

International Nuclear Information System (INIS)

Almeida, Cirila Tacconi de

2005-01-01

The U-Mo-Al dispersion fuels of Material Test Reactors (MTR) are analyzed in terms of their irradiation performance. The irradiation performance aspects are associated to the neutronic and thermal hydraulics aspects to propose a new core configuration to the IEA-R1 reactor of IPEN-CNEN/SP using U-Mo-Al fuels. Core configurations using U-10Mo-Al fuels with uranium densities variable from 3 to 8 gU/cm 3 were analyzed with the computational programs Citation and MTRCR-IEA R1. Core configurations for fuels with uranium densities variable from 3 to 5 gU/cm 3 showed to be adequate to use in IEA-R1 reactor e should present a stable in reactor performance even at high burn-up. (author)

Quantitative determination of uranium distribution homogeneity in MTR fuel type plates

International Nuclear Information System (INIS)

Ferrufino, Felipe Bonito Jaldin

2011-01-01

IPEN/CNEN-SP produces the fuel to supply its nuclear research reactor IEA-R1. The fuel is assembled with fuel plates containing an U 3 Si 2 -Al composite meat. A good homogeneity in the uranium distribution inside the fuel plate meat is important from the standpoint of irradiation performance. Considering the lower power of reactor IEA-R1, the uranium distribution in the fuel plate has been evaluated only by visual inspection of radiographs. However, with the possibility of IPEN to manufacture the fuel for the new Brazilian Multipurpose Reactor (RMB), with higher power, it urges to develop a methodology to determine quantitatively the uranium distribution into the fuel. This paper presents a methodology based on X-ray attenuation, in order to quantify the uranium concentration distribution in the meat of the fuel plate by using optical densities in radiographs and comparison with standards. The results demonstrated the inapplicability of the method, considering the current specification for the fuel plates due to the high intrinsic error to the method. However, the study of the errors involved in the methodology, seeking to increase their accuracy and precision, can enable the application of the method to qualify the final product. (author)

Determination of carbon chlorine and fluorine in uranium dioxide

International Nuclear Information System (INIS)

Kijko, N.I.; Timofeev, G.A.

1983-01-01

Techniques of chlorine and fluorine determination and simultaneous determination of carbon and chlorine in electrolytic uranium dioxide are described. The method of chlorine and fluorine determination is based on their separation during oxide pyrohydrolysis with subsequent spectrophotometric analysis of condensate. Lower determination limits constitute 1 μg for chlorine, 0.5 μg for fluorine. Relative standard deviation when the content of impurities analyzed is 10 -3 % constitutes 0.05-0.07

Comparison of uranium dissolution rates from spent fuel and uranium dioxide

International Nuclear Information System (INIS)

Steward, S.A.; Gray, W.J.

1994-01-01

Two similar sets of dissolution experiments, resulting from a statistical experimental design were performed in order to examine systematically the effects of temperature (25--75 degree C), dissolved oxygen (0.002-0.2 atm overpressure), pH (8--10) and carbonate concentrations (2--200 x 10 -4 molar) on aqueous dissolution of UO 2 and spent fuel. The average dissolution rate was 8.6 mg/m 2 ·day for UO 2 and 3.1 mg/m 2 ·day for spent fuel. This is considered to be an insignificant difference; thus, unirradiated UO 2 and irradiated spent fuel dissolved at about the same rate. Moreover, regression analyses indicated that the dissolution rates of UO 2 and spent fuel responded similarly to changes in pH, temperature, and carbonate concentration. However, the two materials responded very differently to dissolved oxygen concentration. Approximately half-order reaction rates with respect to oxygen concentration were found for UO 2 at all conditions tested. At room temperature, spent fuel dissolution (reaction) rates were nearly independent of oxygen concentration. At 75 degree C, reaction orders of 0.35 and 0.73 were observed for spent fuel, and there was some indication that the reaction order with respect to oxygen concentration might be dependent on pH and/or carbonate concentration as well as on temperature

Status of fuel element technology for plate type dispersion fuels with high uranium density

International Nuclear Information System (INIS)

Hrovat, M.; Huschka, H.; Koch, K.H.; Nazare, S.; Ondracek, G.

1983-01-01

A number of about 20 Material Test and Research Reactors in Germany and abroad is supplied with fuel elements by the company NUKEM. The power of these reactors differs widely ranging from up to about 100 MW. Consequently, the uranium density of the fuel elements in the meat varies considerably depending on the reactor type and is usually within the range from 0.4 to 1.3 g U/cm 3 if HEU is used. In order to convert these reactors to lower uranium enrichment (19.75% 235-U) extensive work is carried out at NUKEM since about two years with the goal to develop fuel elements with high U-density. This work is sponsored by the German Ministry for Research and Technology in the frame of the AF-program. This paper reports on the present state of development for fuel elements with high U-density fuels at NUKEM is reported. The development works were so far concentrated on UAl x , U 3 O 8 and UO 2 fuels which will be described in more detail. In addition fuel plates with new fuels like e.g. U-Si or U-Fe compounds are developed in collaboration with KfK. The required uranium densities for some typical reactors with low, medium, and high power are listed allowing a comparison of HEU and LEU uranium density requirements. The 235-U-content in the case of LEU is raised by 18%. Two different meat thicknesses are considered: Standard thickness of 0.5 mm; and increased thickness of 0.76 mm. From this data compilation the objective follows: in the case of conversion to LEU (19.75% 235-U-enrichment), uranium densities have to be made available up to 24 gU/cm 3 meat for low power level reactors, up to 33 gU/cm 3 meat for medium power level reactors, and between 5.75 and 7.03 g/cm 3 meat for high power level reactors according to this consideration

A Study on Silicide Coatings as Diffusion barrier for U-7Mo Dispersion Fuel

Energy Technology Data Exchange (ETDEWEB)

Won, Ju Jin; Kim, Sung Hwan; Lee, Kyu Hong; Jeong, Yong Jin; Kim, Ki Nam; Park, Jong Man; Lee, Chong Tak [KAERI, Daejeon (Korea, Republic of)

2016-05-15

Gamma phase U-Mo alloys are regarded as one of the promising candidates for advanced research reactor fuel when it comes to the irradiation performance. However, it has been reported that interaction layer formation between the UMo alloys and Al matrix degrades the irradiation performance of U-Mo dispersion fuel. The excessive interaction between the U-Mo alloys and their surrounding Al matrix lead to excessive local swelling called 'pillowing'. For this reason, KAERI suggested several remedies such as alloying U-Mo with Al matrix with Si. In addition, silicide or nitride coatings on the surface of U-Mo particles have also been proposed to hinder the growth of the interaction layer. In this study, centrifugally atomized U-7Mo alloy powders were coated with silicide layers at 900 .deg. C for 1hr. U-Mo alloy powder was mixed with MoSi{sub 2}, Si and ZrSi{sub 2} powders and subsequently heat-treated to form uranium-silicide coating layers on the surface of U-Mo alloy particles. Silicide coated U-Mo powders and characterized using scanning electron microscopy (SEM), energy dispersive x-ray spectroscopy (EDS) and X-ray diffractometer (XRD). The ZrSi{sub 2} coating layers has a thickness of about 1∼ 2μm. The surface of a silicide coated particle was very rough and silicide powder attached to the surface of the coating layer. 3. The XRD analysis of the coating layers showed that, they consisted of compounds such as U3Si{sub 2}, USi{sub 2}.

Method for providing uranium articles with a corrosion resistant anodized coating

International Nuclear Information System (INIS)

Waldrop, F.B.; Washington, C.A.

1982-01-01

Uranium articles are provided with anodized oxide coatings in an aqueous solution of an electrolyte selected from the group consisting of potassium phosphate, potassium hydroxide, ammonium hydroxide, and a mixture of potassium tetraborate and boric acid. The uranium articles are anodized at a temperature greater than about 75 degrees C. With a current flow of less than about 0.036 A/cm2 of surface area while the Ph of the solution is maintained in a range of about 2 to 11.5. The Ph values of the aqueous solution and the low current density utilized during the electrolysis prevent excessive dissolution of the uranium and porosity in the film or watering. The relatively high temperature of the electrolyte bath inhibits hydration and the attendant deleterious pitting so as to enhance corrosion resistance of the anodized coating

Spent fuel reprocessing method

International Nuclear Information System (INIS)

Shoji, Hirokazu; Mizuguchi, Koji; Kobayashi, Tsuguyuki.

1996-01-01

Spent oxide fuels containing oxides of uranium and transuranium elements are dismantled and sheared, then oxide fuels are reduced into metals of uranium and transuranium elements in a molten salt with or without mechanical removal of coatings. The reduced metals of uranium and transuranium elements and the molten salts are subjected to phase separation. From the metals of uranium and transuranium elements subjected to phase separation, uranium is separated to a solid cathode and transuranium elements are separated to a cadmium cathode by an electrolytic method. Molten salts deposited together with uranium to the solid cathode, and uranium and transuranium elements deposited to the cadmium cathode are distilled to remove deposited molten salts and cadmium. As a result, TRU oxides (solid) such as UO 2 , Pu 2 in spent fuels can be reduced to U and TRU by a high temperature metallurgical method not using an aqueous solution to separate them in the form of metal from other ingredients, and further, metal fuels can be obtained through an injection molding step depending on the purpose. (N.H.)

Fabrication of uranium dioxide of different granulation from uranyl nitrate by ammonia diuranate; Dobijanje urandioksida razlicitih granulacija iz uranilnitrata preko amonijumdiuranata

Energy Technology Data Exchange (ETDEWEB)

Vojnovic, J; Stamenkovic, I [Institute of Nuclear Sciences Boris Kidric, Laboratorija za termotehniku reaktora, Vinca, Beograd (Serbia and Montenegro)

1961-12-15

Uranium dioxide is most frequently produced by reduction of higher oxides (UO{sub 3}, U{sub 3}O{sub 8}) or reduction of uranium salts (uranium diuranate, uranium peroxide, uranyl oxalate). Reduction is most frequently done in hydrogen or carbon monoxide atmosphere under temperatures from 500 - 1700 deg C. One of the most frequently methods for producing uranium oxide is certainly reduction of ammonia diuranate by hydrogen (ADU method). Properties of uranium dioxide obtained by ADU method depend on properties of the initial substance. Investigations shown in this report are concerned with determining the properties of UO{sub 2} powders for determining the connection between their properties and conditions of fabrication and reduction of ADU and U{sub 3}O{sub 8}.

Canada's nuclear fuel industry: An overview. Background paper

International Nuclear Information System (INIS)

Nixon, A.

1993-11-01

Canada was among the first countries to mine and process uranium-bearing ores. Such ores contain trace amounts of radium, which was in great demand for medical treatment and for use by research laboratories in the early part of the century. For the last half century, the same basic processes have been used to extract uranium from its ores and convert it to a form suitable for use in nuclear reactors. The process described here is that currently in use in Canada. Mining can take a variety of forms, from open-pit to deep, hard-rock. Mining is typically the most costly step in the process, particularly for lower-grade ores. The ore is crushed and ground in the mill to the consistency of fine sand from which the uranium is extracted chemically to produce the impure concentrate known as yellowcake. In the next step, the impure uranium concentrate is chemically refined into highly purified, nuclear-grade, uranium trioxide (UO 3 ). Uranium trioxide is then converted, in two separate chemical processes, into uranium dioxide (UO 2 ) which is destined for domestic consumption and uranium hexafluoride (UF 6 ) which is exported. In Canada, fabrication is the final step of the fuel production process. Uranium dioxide powder is compressed and sintered into very dense ceramic pellets which are then sealed in zirconium tubes and assembled into fuel bundles for Candu reactors. This background paper will review the Canadian nuclear fuels industry. 1 fig

Study the polymer coating for detecting and surface decontamination of uranium

International Nuclear Information System (INIS)

Pham Thi Quynh Luong; Nguyen Van Chinh

2011-01-01

Strippable polymer coating is one of the methods for effective surface decontamination. It has been developed in both detecting and removing the radioactive isotope and heavy metal elements from contaminated surfaces. A polymer coating is produced to be sprayed or brushed on contaminated material of uranium. The places of U contamination is shown by color change of polymer coating. As the polymer coating is dried up to form a strong film, the contaminations are absorbed in to the coating and contaminated surfaces are cleaned by removing the film. (author)

Development of coated particle fuel technology

International Nuclear Information System (INIS)

Cho, Moonsung; Kim, B. G.; Kim, D. J.

2011-06-01

Ammonia contacting method for prehardenning the surfaces of ADU liquid droplets and the ageing/washing/drying method and equipment for spherical dried-ADU particles were improved and tested with laboratory sacle. After the improvement of fabrication process, the sphericity of UO 2 kernel obtained to 1.1, and the sintered density and O/U ratio of final UO 2 kernel were above 10.60g/cm 3 . 2.01 respectively. Defects of SiC coating layer could be minimized by optimization of gas flow rate. The fracture strength of SiC layer increased from 450 MPa to 530 MPa by controlling the coating defects. An effort was made to develop the fundamental technology for the fuel element compact for use in High Temperature Gas-cooled Reactor(HTGR) through an establishment of fabrication process, required materials and process equipment as well as performing experiments to identify the basic process conditions and optimize them. Thermal load simulation and verification experiments were carried out for an assesment of the design feasibility of the irradiation rod. Out-of-pile testing of irradiation device such as measurement of pressure drop and vibration, endurance test was performed and the validity of its design was confirmed. A fuel performance analysis code, COPA has been developed to calculate the fuel temperature, the failure fractions of coated fuel particles, the release of fission products. The COPA code can be used to evaluate the performance of the high temperature reactor fuel under the reactor operation, irradiation, heating conditions. KAERI participated in the round robin test of IAEA CRP-6 program to characterize the diameter, sphericity, coating thickness, density and anisotropy of coated particles provided by Korea, USA and South Africa. QC technology was established for TRISO-coated fuel particle. A method for accurate measurement of the optical anisotropy factor for PyC layers of coated particles was developed. Technology and inspection procedures for density

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

International Nuclear Information System (INIS)

Heckendorn, F.M.

2001-01-01

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

Behavior of metallic uranium-fissium fuel in TREAT transient overpower tests

International Nuclear Information System (INIS)

Bauer, T.H.; Klickman, A.E.; Lo, R.K.; Rhodes, E.A.; Robinson, W.R.; Stanford, G.S.; Wright, A.E.

1986-01-01

TREAT tests M2, M3, and M4 were performed to obtain information on two key behavior characteristics of fuel under transient overpower accident conditions in metal-fueled fast reactors: the prefailure axial self-extrusion (elongation beyond thermal expansion) of fuel within intact cladding and the margin to cladding breach. Uranium-5 wt% fissium Experimental Breeder Reactor-II driver fuel pins were used for the tests since they were available as suitable stand-ins for the uranium-plutonium-zirconium ternary fuel, which is the reference fuel of the integral fast reactor (IFR) concept. The ternary fuel will be used in subsequent TREAT tests. Preliminary results from tests M2 and M3 were presented earlier. The present report includes significant advances in analysis as well as additional data from test M4. Test results and analysis have led to the development and validation of pin cladding failure and fuel extrusion models for metallic fuel, within reasonable uncertainties for the uranium-fissium alloy. Concepts involved are straightforward and readily extendable to ternary alloys and behavior in full-size reactors

Irradiation testing of coated particle fuel at Hanaro

International Nuclear Information System (INIS)

Goo Kim, Bong; Sung Cho, Moo; Kim, Yong Wan

2014-01-01

TRISO-coated particle fuel is developing to support development of VHTR in Korea. From August 2013, the first irradiation testing of coated particle fuel was begun to demonstrate and qualify TRISO fuel for use in VHTR in the HANARO at KAERI. This experiment is currently undergoing under the atmosphere of a mixed inert gas without on-line temperature monitoring and control combined with on-line fission product monitoring of the sweep gas. The irradiation device contains two test rods, one contains nine fuel compacts and the other five compacts and eight graphite specimens. Each compact has 263 coated particles. After a peak burn-up of about 4 at% and a peak fast neutron fluence of about 1.7 x 10 21 n/cm 2 , PIE will be carried out at KAERI's Irradiated Material Examination Facility. This paper is described characteristics of coated particle fuel, the design of test rod and irradiation device for coated particle fuel, discusses the technical results for irradiation testing at HANARO. (authors)

Fabrication routes for Thorium and Uranium233 based AHWR fuel

International Nuclear Information System (INIS)

Danny, K.M.; Saraswat, Anupam; Chakraborty, S.; Somayajulu, P.S.; Kumar, Arun

2011-01-01

India's economic growth is on a fast growth track. The growth in population and economy is creating huge demand for energy which has to be met with environmentally benign technologies. Nuclear Energy is best suited to meet this demand without causing undue environmental impact. Considering the large thorium reserves in India, the future nuclear power program will be based on Thorium- Uranium 233 fuel cycle. The major characteristic of thorium as the fuel of future comes from its superior fuel utilization. 233 U produced in a reactor is always contaminated with 232 U. This 232 U undergoes a decay to produce 228 Th and it is followed by decay chain including 212 Bi and 208 Tl. Both 212 Bi and 208 Tl are hard gamma emitters ranging from 0.6 MeV-1.6 MeV and 2.6 MeV respectively, which necessitates its handling in hot cell. The average concentration of 232 U is expected to exceed 1000 ppm after a burn-up of 24,000 MWD/t. Work related to developing the fuel fabrication technology including automation and remotization needed for 233 U based fuels is in progress. Various process for fuel fabrication have been developed i.e. Coated Agglomerate Pelletisation (CAP), impregnation technique (Pellet/Gel), Sol Gel Micro-sphere Pelletisation (SGMP) apart from Powder to Pellet (POP) route. This paper describes each process with respect to its advantages, disadvantages and its amenability to automation and remotisation. (author)

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)

Modified ADS molten salt processes for back-end fuel cycle of PWR spent fuel

International Nuclear Information System (INIS)

Choi, In-Kyu; Yeon, Jei-Won; Kim, Won-Ho

2002-01-01

The back-end fuel cycle concept for PWR spent fuel is explained. This concept is adequate for Korea, which has operated both PWR and CANDU reactors. Molten salt processes for accelerator driven system (ADS) were modified both for the transmutation of long-lived radioisotopes and for the utilisation of the remained fissile uranium in PWR spent fuels. Prior to applying molten salt processes to PWR fuel, hydrofluorination and fluorination processes are applied to obtain uranium hexafluoride from the spent fuel pellet. It is converted to uranium dioxide and fabricated into CANDU fuel. From the remained fluoride compounds, transuranium elements can be separated by the molten salt technology such as electrowinning and reductive extraction processes for transmutation purpose without weakening the proliferation resistance of molten salt technology. The proposed fuel cycle concept using fluorination processes is thought to be adequate for our nuclear program and can replace DUPIC (Direct Use of spent PWR fuel in CANDU reactor) fuel cycle. Each process for the proposed fuel cycle concept was evaluated in detail

Fuel element

International Nuclear Information System (INIS)

Armijo, J.S.

1976-01-01

A fuel element for nuclear reactors is proposed which has a higher corrosion resisting quality in reactor operations. The zirconium alloy coating around the fuel element (uranium or plutonium compound) has on its inside a protection layer of metal which is metallurgically bound to the substance of the coating. As materials are namned: Alluminium, copper, niobium, stainless steel, and iron. This protective metallic layer has another inner layer, also metallurgically bound to its surface, which consists usually of a zirconium alloy. (UWI) [de

Fabrication procedures for manufacturing high uranium concentration dispersion fuel elements

International Nuclear Information System (INIS)

Souza, Jose Antonio Batista de

2011-01-01

IPEN-CNEN/SP developed the technology to produce the dispersion type fuel elements for research reactors and made it available for routine production. Today, the fuel produced in IPEN-CNEN/SP is limited to the uranium concentration of 3.0 gU/cm 3 for U 3 Si 2 -Al dispersion-based and 2.3 gU/cm 3 for U 3 O 8 -Al dispersion. The increase of uranium concentration in fuel plates enables the reactivity of the reactor core reactivity to be higher and extends the fuel life. Concerning technology, it is possible to increase the uranium concentration in the fuel meat up to the limit of 4.8 gU/cm 3 in U 3 Si 2 -Al dispersion and 3.2 gU/cm 3 U 3 O 8 -Al dispersion. These dispersions are well qualified worldwide. This work aims to develop the manufacturing process of both fuel meats with high uranium concentrations, by redefining the manufacturing procedures currently adopted in the Nuclear Fuel Center of IPEN-CNEN/SP. Based on the results, it was concluded that to achieve the desired concentration, it is necessary to make some changes in the established procedures, such as in the particle size of the fuel powder and in the feeding process inside the matrix, before briquette pressing. These studies have also shown that the fuel plates, with a high concentration of U 3 Si 2 -Al, met the used specifications. On the other hand, the appearance of the microstructure obtained from U 3 O 8 -Al dispersion fuel plates with 3.2 gU/cm 3 showed to be unsatisfactory, due to the considerably significant porosity observed. The developed fabrication procedure was applied to U 3 Si 2 production at 4.8 gU/cm 3 , with enriched uranium. The produced plates were used to assemble the fuel element IEA-228, which was irradiated in order to check its performance in the IEA-R1 reactor at IPEN-CNEN/SP. These new fuels have potential to be used in the new Brazilian Multipurpose Reactor - RMB. (author)

Study and development of refractory coatings for metallic uranium fusion and evaporation

International Nuclear Information System (INIS)

Vasconcelos, Getulio de

2004-01-01

In melting process or evaporation of metallic uranium, the reaction with the crucible and the possible contamination of the molten metal should be avoided. This effect can be reduced using an inert and protective coating on the crucible walls. The selection of the coating should be based on the chemical inertia and the kinetic of the reaction products. By avoiding chemical reactions, the amount of impurities in the molten metal can be reduced, leading to an increased crucible lifetime. This work presents a comparative study among different crucible coatings used in the melting process of metallic uranium, at temperatures above its melting point. Samples of metallic uranium are melted in contact with different materials in a vacuum furnace. The reactions occur at a given temperature during a certain time interval; samples are then cooled down to room temperature. Finally, samples are characterized by optical and electronic microscopy, dispersive X-ray spectroscopy, surface roughness and X-ray diffraction. Samples preparation consists of polishing selected areas, and milling the reaction products originated from the corroded interfaces. The extent of the reactions is determined as a function of the temperature by optical microscopy and roughness analyses. The compositions of the reacted products are determined by Energy Dispersive Spectroscopy, and the phase changes by X-ray diffraction. The results indicate that alumina presented higher activation energy (39 kcal.mol -1 ) than magnesia (12 kcal.mol -1 ), otherwise, it is corroded faster. On the other hand, the alumina could be protected by a thick coating of titanium nitride, because no rection between titanium nitride and uranium was observed at temperatures near to 1700 K. After cooling to the room temperature, there is stress concentration between the graphite and the TiN layer, generating a compressive stress of 0,5 GPa. When uranium is deposited on the TiN, a tensile stress is generated in this new layer, which

Back-end fuel cycle efficiencies with respect to improved uranium utilization

International Nuclear Information System (INIS)

Kuczera, B.; Hennies, H.H.

1983-01-01

The world-wide nuclear power plant (NPP) capacity is at present 160 GW(e). If one adds the power stations under construction and ordered, a plant capacity of approximately 480 GW(e) is obtained for 1990, with the share of LWRs making up more than 80%. A modern LWR consumes in the open fuel cycle about 4400 metric tonnes of natural uranium per GW(e), assuming a lifetime of 30 years and a load factor of 70%. Considering the natural uranium reserves known at present and exploitable under economic conditions, it can be conveniently estimated that, with the present NPP capacity extension perspective, the natural uranium resources may be exhausted in a few decades. This trend can be counteracted in a flexible manner by various approaches in fuel cycle technology and strategy: (i) by steady further development of the established LWR technology the uranium consumption can be reduced by about 15%; (ii) closing the nuclear fuel cycle on the basis of LWRs (i.e. thermal uranium and plutonium recycling) implies up to 40% savings in natural uranium consumption; (iii) more recent considerations include the advanced pressurized water reactor (APWR). The APWR combines the proven PWR technology with a newly developed tight lattice core with greatly improved conversion characteristics (conversion ratio = 0.90 to 0.95). In terms of uranium utilization, the APWR has an efficiency three to five times higher than a PWR; (iv) Commercial introduction of FBR systems results in an optimal utilization of uranium which, at the same time, guarantees the supply of nuclear fuel well beyond the present century. For a corresponding transition period an energy supply system can be conceived which relies essentially on extended back-end fuel cycle capacities. These would facilitate a symbiosis of PWR, APWR and FBR, characterized by high flexibility with respect to long-term developments on the energy market. (author)

Mixed U/Pu oxide fuel fabrication facility co-processed feed, pelletized fuel

International Nuclear Information System (INIS)

1978-09-01

Two conceptual MOX fuel fabrication facilities are discussed in this study. The first facility in the main body of the report is for the fabrication of LWR uranium dioxide - plutonium dioxide (MOX) fuel using co-processed feed. The second facility in the addendum is for the fabrication of co-processed MOX fuel spiked with 60 Co. Both facilities produce pellet fuel. The spiked facility uses the same basic fabrication process as the conventional MOX plant but the fuel feed incorporates a high energy gamma emitter as a safeguard measure against diversion; additional shielding is added to protect personnel from radiation exposure, all operations are automated and remote, and normal maintenance is performed remotely. The report describes the fuel fabrication process and plant layout including scrap and waste processing; and maintenance, ventilation and safety measures

The use of medium enriched uranium fuel for research reactors

International Nuclear Information System (INIS)

1979-01-01

The evaluation described in the present paper concerns the use of medium enriched uranium fuel for our research reactors. The underlying assumptions set up for the evaluation are as follows: (1) At first, the use of alternative fuel should not affect, even to a small extent, research and development programs in nuclear energy utilization, which were described in the previous paper. Hence the use of lower enrichment fuel should not cause any reduction in reactor performances. (2) The fuel cycle cost for operating research reactors with alternative fuel, excepting R and D cost for such fuel, should not increase beyond an acceptable limit. (3) The use of alternative fuel should be satisfactory with respect to non-proliferation purposes, to the almost same degree as the use of 20% enriched uranium fuel

Natural uranium equivalent fuel an innovative design for proven CANDU technology

Energy Technology Data Exchange (ETDEWEB)

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

2015-07-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2015-09-15

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

Aqueous dissolution rates of uranium oxides

International Nuclear Information System (INIS)

Steward, S.A.; Mones, E.T.

1994-10-01

An understanding of the long-term dissolution of waste forms in groundwater is required for the safe disposal of high level nuclear waste in an underground repository. The main routes by which radionuclides could be released from a geological repository are the dissolution and transport processes in groundwater flow. Because uranium dioxide is the primary constituent of spent nuclear fuel, the dissolution of its matrix in spent fuel is considered the rate-limiting step for release of radioactive fission products. The purpose of our work has been to measure the intrinsic dissolution rates of uranium oxides under a variety of well-controlled conditions that are relevant to a repository and allow for modeling. The intermediate oxide phase U 3 O 8 , triuranium octaoxide, is quite stable and known to be present in oxidized spent fuel. The trioxide, UO 3 , has been shown to exist in drip tests on spent fuel. Here we compare the results of essentially identical dissolution experiments performed on depleted U 3 O 8 and dehyrated schoepite or uranium trioxide monohydrate (UO 3 ·H 2 O). These are compared with earlier work on spent fuel and UO 2 under similar conditions

Milling uranium silicide powder for dispersion nuclear fuels

Energy Technology Data Exchange (ETDEWEB)

Vieira, E.; Silva, D.G.; Souza, J.A.B.; Durazzo, M. [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil); Riella, H.G. [Universidade Federal de Santa Catarina (UFSC), Florianopolis, SC (Brazil)

2009-07-01

Full text: Uranium silicide (U3Si2) is presently considered the best fuel qualified so far in terms of uranium loading and performance. Stability of the U3Si2 fuel with uranium density of 4.8 g/cm3 was confirmed by burnup stability tests performed during the Reduced Enrichment for Research and Test Reactors (RERTR) program. This fuel was chosen to compose the first core of the new Brazilian Multipurpose Research Reactor (RMB), planned to be constructed in the next years. This new reactor will consume bigger quantities of U3Si2 powder, when compared with the small consumption of the IEA-R1 research reactor of IPEN-CNEN/SP, the unique MTR type research reactor operating in the country. At the present time, the milling operation of U3Si2 ingots is made manually. In order to increase the powder production capacity, the manual milling must be replaced by an automated procedure. This paper describes a new milling machine and procedure developed to produce U3Si2 powder with higher efficiency. (author)

Preliminary concepts: coordinated safeguards for materials management in a thorium--uranium fuel reprocessing plant

International Nuclear Information System (INIS)

Hakkila, E.A.; Barnes, J.W.; Dayem, H.A.; Dietz, R.J.; Shipley, J.P.

1978-10-01

This report addresses preliminary concepts for coordinated safeguards materials management in a typical generic thorium--uranium-fueled light-water reactor (LWR) fuels reprocessing plant. The reference facility is designed to recover thorium and uranium from first-generation (denatured 235 U) startup fuels, first-recycle and equilibrium (denatured 233 U) thorium--uranium LWR fuels, and to recover the plutonium generated in the 238 U denaturant as well. 12 figures, 3 tables

Reactivity feedbacks of a material test research reactor fueled with various low enriched uranium dispersion fuels

International Nuclear Information System (INIS)

Muhammad, Farhan; Majid, Asad

2009-01-01

The reactivity feedbacks of a material test research reactor using various low enriched uranium fuels, having same uranium density were calculated. For this purpose, the original aluminide fuel (UAl x -Al) containing 4.40 gU/cm 3 of an MTR was replaced with silicide (U 3 Si-Al and U 3 Si 2 -Al) and oxide (U 3 O 8 -Al) dispersion fuels having the same uranium density as of the original fuel. Calculations were carried out to find the fuel temperature reactivity feedback, moderator temperature reactivity feedback, moderator density reactivity feedback and moderator void reactivity feedback. Nuclear reactor analysis codes including WIMS-D4 and CITATION were employed to carry out these calculations. It was observed that the magnitudes all the respective reactivity feedbacks from 38 deg. C to 50 deg. C and 100 deg. C, at the beginning of life, of all the fuels were very close to each other. The fuel temperature reactivity feedback of the U 3 O 8 -Al was about 2% more than the original UAl x -Al fuel. The magnitudes of the moderator temperature, moderator density and moderator void reactivity feedbacks of all the fuels, showed very minor variations from the original aluminide fuel.

Pilot production of 325 kg of uranium carbide

International Nuclear Information System (INIS)

Clozet, C.; Dessus, J.; Devillard, J.; Guibert, M.; Morlot, G.

1969-01-01

This report describes the pilot fabrication of uranium carbide rods to be mounted in bundles and assayed in two channels of the EL 4 reactor. The fabrication process includes: - elaboration of uranium carbide granules by carbothermic reduction of uranium dioxide; - electron bombardment melting and continuous casting of the granules; - machining of the raw ingots into rods of the required dimensions; finally, the rods will be piled-up to make the fuel elements. Both qualitative and quantitative results of this pilot production chain are presented and discussed. (authors) [fr

Evolution of spent nuclear fuel in dry storage conditions for millennia and beyond

Energy Technology Data Exchange (ETDEWEB)

Wiss, Thierry, E-mail: thierry.wiss@ec.europa.eu [European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O. Box 2340, 76125 Karlsruhe (Germany); Hiernaut, Jean-Pol [European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O. Box 2340, 76125 Karlsruhe (Germany); Roudil, Danièle [Commissariat à l’Energie Atomique et aux Energie Alternatives, Centre de Marcoule, BP 30207 Bagnols-sur-Cèze (France); Colle, Jean-Yves; Maugeri, Emilio; Talip, Zeynep; Janssen, Arne; Rondinella, Vincenzo; Konings, Rudy J.M.; Matzke, Hans-Joachim [European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O. Box 2340, 76125 Karlsruhe (Germany); Weber, William J. [Department of Materials Science and Engineering, The University of Tennessee, Knoxville, TN 37996 (United States); Division of Materials Science and Technology, Oak Ridge National Laboratory, Oak Ridge, TN 37831 (United States)

2014-08-01

Significant amounts of spent uranium dioxide nuclear fuel are accumulating worldwide from decades of commercial nuclear power production. While such spent fuel is intended to be reprocessed or disposed in geologic repositories, out-of-reactor radiation damage from alpha decay can be detrimental to its structural stability. Here we report on an experimental study in which radiation damage in plutonium dioxide, uranium dioxide samples doped with short-lived alpha-emitters and urano-thorianite minerals have been characterized by XRD, transmission electron microscopy, thermal desorption spectrometry and hardness measurements to assess the long-term stability of spent nuclear fuel to substantial alpha-decay doses. Defect accumulation is predicted to result in swelling of the atomic structure and decrease in fracture toughness; whereas, the accumulation of helium will produce bubbles that result in much larger gaseous-induced swelling that substantially increases the stresses in the constrained spent fuel. Based on these results, the radiation-ageing of highly-aged spent nuclear fuel over more than 10,000 years is predicted.

Separation and recovery method for depleted uranium from spent fuel

International Nuclear Information System (INIS)

Imoto, Yoshie; Fujita, Reiko.

1993-01-01

Spent oxide fuels are reduced in a molten salt of CaCl 2 -CaF 2 to convert them into metals, then melted in an Fe-U bath disposed in an electrolytic refining vessel and brought into contact with molten Mg, to extract transuranium elements and rare earth elements contained in the Fe-U bath as metals in the molten Mg. Then molten Mg is removed and the residue is brought into contact with KCl-LiCl molten salt and electrolyzed using the Fe-U as an anode. Then, uranium is recovered by deposition on an iron cathode disposed in chloride electrolytes of the electrolytic refining vessel. Uranium and transuranium elements can be thus separated and, for example, depleted uranium for use in blanket fuels can be recovered easily. This can greatly reduce the temporary storage amount of depleted uranium, to eliminate requirement for a large-scaled facility used exclusively for storing uranium and long time management for uranium. (T.M.)

The Fabrication Problem Of U3Si2-Al Fuel With Uranium High Loading

International Nuclear Information System (INIS)

Supardjo

1996-01-01

The quality of U 3 Si 2 -Al dispersion fuel product is the main aim for each fabricator. Low loading of uranium fuel element is easily fabricated, but with the increased, uranium loading, homogeneity of uranium distribution is difficult to achieve and it always formed white spots, blister, and dogboning in the fuel plates. The problem can be eliminated by the increasing treatment of the fuel/Al powder. The precise selection of fuel/Al particles diameter is needed indeed to make easier in the homogeneous process of powder and the porosities arrangement in the fuel plates. The increasing of uranium loading at constant meat thickness will increase the meat hardness, therefore to withdraw the dogboning forming, the use of harder cladding materials is necessity

Fuel swelling and interaction layer formation in the SELENIUM Si and ZrN coated U(Mo) dispersion fuel plates irradiated at high power in BR2

Science.gov (United States)

Leenaers, A.; Van den Berghe, S.; Koonen, E.; Kuzminov, V.; Detavernier, C.

2015-03-01

In the framework of the SELENIUM project two full size flat fuel plates were produced with respectively Si and ZrN coated U(Mo) particles and irradiated in the BR2 reactor at SCK•CEN. Non-destructive analysis of the plates showed that the fuel swelling profiles of both SELENIUM plates were very similar to each other and none of the plates showed signs of pillowing or excessive swelling at the end of irradiation at the highest power position (local maximum 70% 235U). The microstructural analysis showed that the Si coated fuel has less interaction phase formation at low burn-up but at the highest burn-ups, defects start to develop on the IL-matrix interface. The ZrN coated fuel, shows a virtual absence of reaction between the U(Mo) and the Al, up to high fission densities after which the interaction layer formation starts and defects develop in the matrix near the U(Mo) particles. It was found and is confirmed by the SELENIUM (Surface Engineering of Low ENrIched Uranium-Molybdenum) experiment that there are two phenomena at play that need to be controlled: the formation of an interaction layer and swelling of the fuel. As the interaction layer formation occurs at the U(Mo)-matrix interface, applying a diffusion barrier (coating) at that interface should prevent the interaction between U(Mo) and the matrix. The U(Mo) swelling, observed to proceed at an accelerating rate with respect to fission density accumulation, is governed by linear solid state swelling and fission gas bubble swelling due to recrystallization of the fuel. The examination of the SELENIUM fuel plates clearly show that for the U(Mo) dispersion fuel to be qualified, the swelling rate at high burn-up needs to be reduced.

Recent irradiation tests of uranium-plutonium-zirconium metal fuel elements

International Nuclear Information System (INIS)

Pahl, R.G.; Lahm, C.E.; Villarreal, R.; Hofman, G.L.; Beck, W.N.

1986-09-01

Uranium-Plutonium-Zirconium metal fuel irradiation tests to support the ANL Integral Fast Reactor concept are discussed. Satisfactory performance has been demonstrated to 2.9 at.% peak burnup in three alloys having 0, 8, and 19 wt % plutonium. Fuel swelling measurements at low burnup in alloys to 26 wt % plutonium show that fuel deformation is primarily radial in direction. Increasing the plutonium content in the fuel diminishes the rate of fuel-cladding gap closure and axial fuel column growth. Chemical redistribution occurs by 2.1 at.% peak burnup and generally involves the inward migration of zirconium and outward migration of uranium. Fission gas release to the plenum ranges from 46% to 56% in the alloys irradiated to 2.9 at.% peak burnup. No evidence of deleterious fuel-cladding chemical or mechanical interaction was observed

Sorption behaviour of uranium and thorium on cryptomelane-type hydrous manganese dioxide from aqueous solution

International Nuclear Information System (INIS)

El-Naggar, I.M.; El-Absy, M.A.; Abdel-Hamid, M.M.; Aly, H.F.

1993-01-01

The kinetics of sorption of uranium and thorium from aqueous nitrate solutions on cryptomelane-type hydrous manganese dioxide (CRYMO) was studied. The exchange of uranium is particle diffusion controlled while that of thorium is chemical reaction at the exchange sites. Sorption of uranium and thorium by CRYMO has been also studied as a function of metal concentrations and temperature. The sorption of both cations is found to be an endothermic process and increases markedly with temperature between 30 and 60 degree C. The sorption results have been analysed by the langmuir adsorption isotherm over the entire range of uranium and thorium concentrations investigated. 35 refs., 8 figs., 5 tabs

A synthesis of carbon dioxide emissions from fossil-fuel combustion

Directory of Open Access Journals (Sweden)

R. J. Andres

2012-05-01

Full Text Available This synthesis discusses the emissions of carbon dioxide from fossil-fuel combustion and cement production. While much is known about these emissions, there is still much that is unknown about the details surrounding these emissions. This synthesis explores our knowledge of these emissions in terms of why there is concern about them; how they are calculated; the major global efforts on inventorying them; their global, regional, and national totals at different spatial and temporal scales; how they are distributed on global grids (i.e., maps; how they are transported in models; and the uncertainties associated with these different aspects of the emissions. The magnitude of emissions from the combustion of fossil fuels has been almost continuously increasing with time since fossil fuels were first used by humans. Despite events in some nations specifically designed to reduce emissions, or which have had emissions reduction as a byproduct of other events, global total emissions continue their general increase with time. Global total fossil-fuel carbon dioxide emissions are known to within 10 % uncertainty (95 % confidence interval. Uncertainty on individual national total fossil-fuel carbon dioxide emissions range from a few percent to more than 50 %. This manuscript concludes that carbon dioxide emissions from fossil-fuel combustion continue to increase with time and that while much is known about the overall characteristics of these emissions, much is still to be learned about the detailed characteristics of these emissions.

Extending the world's uranium resources through advanced CANDU fuel cycles

Energy Technology Data Exchange (ETDEWEB)

De Vuono, Tony; Yee, Frank; Aleyaseen, Val; Kuran, Sermet; Cottrell, Catherine

2010-09-15

The growing demand for nuclear power will encourage many countries to undertake initiatives to ensure a self-reliant fuel source supply. Uranium is currently the only fuel utilized in nuclear reactors. There are increasing concerns that primary uranium sources will not be enough to meet future needs. AECL has developed a fuel cycle vision that incorporates other sources of advanced fuels to be adaptable to its CANDU technology.

Development of ammonium uranyl carbonate reduction to uranium dioxide using fluidized bed

International Nuclear Information System (INIS)

Gomes, R.P.; Riella, H.G.

1988-01-01

Laboratory development of Ammonium Uranyl Carbonate (AUC) reduction to uranium dioxide (UO 2 ) using fluidized bed furnace technique is described. The reaction is carried out at 500-550 0 C using hydrogen, liberated from cracking of ammonia, as a reducing agent. As the AUC used is obtained from uranium hexafluoride (UF 6 ) it contains considerable amounts of fluoride ( - 500μgF - /gTCAU) as contaminant. The presence of fluoride leads to high corrosion rates and hence the fluoride concentrations is reduced by pyrohydrolisis of UO 2 . Physical and Chemical proterties of the final product (UO 2 ) obtained were characterized. (author) [pt

Dissolution of nuclear fuel samples for analytical purposes. I

International Nuclear Information System (INIS)

Krtil, J.

1983-01-01

Main attention is devoted to procedures for dissolving fuels based on uranium metal and its alloys, uranium oxides and carbides, plutonium metal, plutonium dioxide, plutonium carbides, mixed PuC-UC carbides and mixed oxides (PuU)O 2 . Data from the literature and experience gained with the dissolution of nuclear fuel samples at the Central Control Laboratory of the Nuclear Research Institute at Rez are given. (B.S.)

Synthetic osteogenic extracellular matrix formed by coated silicon dioxide nanosprings

Directory of Open Access Journals (Sweden)

Hass Jamie L

2012-01-01

Full Text Available Abstract Background The design of biomimetic materials that parallel the morphology and biology of extracellular matrixes is key to the ability to grow functional tissues in vitro and to enhance the integration of biomaterial implants into existing tissues in vivo. Special attention has been put into mimicking the nanostructures of the extracellular matrix of bone, as there is a need to find biomaterials that can enhance the bonding between orthopedic devices and this tissue. Methods We have tested the ability of normal human osteoblasts to propagate and differentiate on silicon dioxide nanosprings, which can be easily grown on practically any surface. In addition, we tested different metals and metal alloys as coats for the nanosprings in tissue culture experiments with bone cells. Results Normal human osteoblasts grown on coated nanosprings exhibited an enhanced rate of propagation, differentiation into bone forming cells and mineralization. While osteoblasts did not attach effectively to bare nanowires grown on glass, these cells propagated successfully on nanosprings coated with titanium oxide and gold. We observed a 270 fold increase in the division rate of osteoblasts when grow on titanium/gold coated nanosprings. This effect was shown to be dependent on the nanosprings, as the coating by themselves did not alter the growth rate of osteoblast. We also observed that titanium/zinc/gold coated nanosprings increased the levels of osteoblast production of alkaline phosphatase seven folds. This result indicates that osteoblasts grown on this metal alloy coated nanosprings are differentiating to mature bone making cells. Consistent with this hypothesis, we showed that osteoblasts grown on the same metal alloy coated nanosprings have an enhanced ability to deposit calcium salt. Conclusion We have established that metal/metal alloy coated silicon dioxide nanosprings can be used as a biomimetic material paralleling the morphology and biology of

Mixed Uranium/Refractory Metal Carbide Fuels for High Performance Nuclear Reactors

International Nuclear Information System (INIS)

Knight, Travis; Anghaie, Samim

2002-01-01

Single phase, solid-solution mixed uranium/refractory metal carbides have been proposed as an advanced nuclear fuel for advanced, high-performance reactors. Earlier studies of mixed carbides focused on uranium and either thorium or plutonium as a fuel for fast breeder reactors enabling shorter doubling owing to the greater fissile atom density. However, the mixed uranium/refractory carbides such as (U, Zr, Nb)C have a lower uranium densities but hold significant promise because of their ultra-high melting points (typically greater than 3700 K), improved material compatibility, and high thermal conductivity approaching that of the metal. Various compositions of (U, Zr, Nb)C were processed with 5% and 10% metal mole fraction of uranium. Stoichiometric samples were processed from the constituent carbide powders, while hypo-stoichiometric samples with carbon-to-metal (C/M) ratios of 0.92 were processed from uranium hydride, graphite, and constituent refractory carbide powders. Processing techniques of cold uniaxial pressing, dynamic magnetic compaction, sintering, and hot pressing were investigated to optimize the processing parameters necessary to produce high density (low porosity), single phase, solid-solution mixed carbide nuclear fuels for testing. This investigation was undertaken to evaluate and characterize the performance of these mixed uranium/refractory metal carbides for high performance, ultra-safe nuclear reactor applications. (authors)

Use of enriched uranium as a fuel in CANDU reactors

International Nuclear Information System (INIS)

Zech, H.J.

1976-08-01

The use of slightly enriched uranium as a fuel in CANDU-reactors is studied in a simple parametric way. The results show the possibility of 1) about 30% savings in natural uranium consumption 2) about 35% increase in the utilization of the natural uranium 3) a decrease in fuelling costs to about 70 - 80% of the normal case of natural uranium fuelling. (orig.) [de

Loading ion exchange resins with uranium for HTGR fuel kernels

International Nuclear Information System (INIS)

Notz, K.J.; Greene, C.W.

1976-12-01

Uranium-loaded ion exchange beads provide an excellent starting material in the production of uranium carbide microspheres for nuclear fuel applications. Both strong-acid (sulfonate) and weak-acid (carboxylate) resins can be fully loaded with uranium from a uranyl nitrate solution utilizing either a batch method or a continuous column technique

Profileration-proof uranium/plutonium and thorium/uranium fuel cycles. Safeguards and non-profileration. 2. rev. ed.

Energy Technology Data Exchange (ETDEWEB)

Kessler, G.

2017-07-01

A brief outline of the historical development of the proliferation problem is followed by a description of the uranium-plutonium nuclear fuel cycle with uranium enrichment, fuel fabrication, the light-water reactors mainly in operation, and the breeder reactors still under development. The next item discussed is reprocessing of spent fuel with plutonium recycling and the future possibility to incinerate plutonium and the minor actinides: neptunium, americium, and curium. Much attention is devoted to the technical and scientific treatment of the IAEA surveillance concept of the uranium-plutonium fuel cycle. In this context, especially the physically possible accuracy of measuring U/Pu flow in the fuel cycle, and the criticism expressed of the accuracy in measuring the plutonium balance in large reprocessing plants of non-nuclear weapon states are analyzed. The second part of the book initially examines the assertion that reactor-grade plutonium could be used to build nuclear weapons whose explosive yield cannot be predicted accurately, but whose minimum explosive yield is still far above that of chemical explosive charges. Methods employed in reactor physics are used to show that such hypothetical nuclear explosive devices (HNEDs) would attain too high temperatures in the required implosion lenses as a result of the heat generated by the Pu-238 isotope always present in reactor plutonium of current light-water reactors. These lenses would either melt or tend to undergo chemical auto-explosion. Limits to the content of the Pu-238 isotope are determined above which such hypothetical nuclear weapons are not feasible on technical grounds. This situation is analyzed for various possibilities of the technical state of the art of making implosion lenses and various ways of cooling up to the use of liquid helium. The outcome is that, depending on the existing state of the art, reactor-grade plutonium from spent fuel elements of light-water reactors with a burnup of 35 to 58

Composition and Distribution of Tramp Uranium Contamination on BWR and PWR Fuel Rods

International Nuclear Information System (INIS)

Schienbein, Marcel; Zeh, Peter; Hurtado, Antonio; Rosskamp, Matthias; Mailand, Irene; Bolz, Michael

2012-09-01

In a joint research project of VGB and AREVA NP GmbH the behaviour of alpha nuclides in nuclear power plants with light water reactors has been investigated. Understanding the source and the behaviour of alpha nuclides is of big importance for planning radiation protection measures for outages and upcoming dismantling projects. Previous publications have shown the correlation between plant specific alpha contamination of the core and the so called 'tramp fuel' or 'tramp uranium' level which is linked to the defect history of fuel assemblies and accordingly the amount of previously washed out fuel from defective fuel rods. The methodology of tramp fuel estimation is based on fission product concentrations in reactor coolant but also needs a good knowledge of tramp fuel composition and in-core distribution on the outer surface of fuel rods itself. Sampling campaigns of CRUD deposits of irradiated fuel assemblies in different NPPs were performed. CRUD analyses including nuclide specific alpha analysis have shown systematic differences between BWR and PWR plants. Those data combined with literature results of fuel pellet investigations led to model improvements showing that a main part of fission products is caused by fission of Pu-239 an activation product of U-238. CRUD investigations also gave a better picture of the in-core composition and distribution of the tramp uranium contamination. It was shown that the tramp uranium distribution in PWR plants is time dependent. Even new fuel assemblies will be notably contaminated after only one cycle of operation. For PWR applies the following logic: the higher the local power the higher the contamination. With increasing burnup the local rod power usually decreases leading to decreasing tramp uranium contamination on the fuel rod surface. This is not applicable for tramp uranium contamination in BWR. CRUD contamination (including the tramp fuel deposits) is much more fixed and is constantly increasing

Nuclear fuels and development of nuclear fuel elements

International Nuclear Information System (INIS)

Sundaram, C.V.; Mannan, S.L.

1989-01-01

Safe, reliable and economic operation of nuclear fission reactors, the source of nuclear power at present, requires judicious choice, careful preparation and specialised fabrication procedures for fuels and fuel element structural materials. These aspects of nuclear fuels (uranium, plutonium and their oxides and carbides), fuel element technology and structural materials (aluminium, zircaloy, stainless steel etc.) are discussed with particular reference to research and power reactors in India, e.g. the DHRUVA research reactor at BARC, Trombay, the pressurised heavy water reactors (PHWR) at Rajasthan and Kalpakkam, and the Fast Breeder Test Reactor (FBTR) at Kalpakkam. Other reactors like the gas-cooled reactors operating in UK are also mentioned. Because of the limited uranium resources, India has opted for a three-stage nuclear power programme aimed at the ultimate utilization of her abundant thorium resources. The first phase consists of natural uranium dioxide-fuelled, heavy water-moderated and cooled PHWR. The second phase was initiated with the attainment of criticality in the FBTR at Kalpakkam. Fast Breeder Reactors (FBR) utilize the plutonium and uranium by-products of phase 1. Moreover, FBR can convert thorium into fissile 233 U. They produce more fuel than is consumed - hence, the name breeders. The fuel parameters of some of the operating or proposed fast reactors in the world are compared. FBTR is unique in the choice of mixed carbides of plutonium and uranium as fuel. Factors affecting the fuel element performance and life in various reactors e.g. hydriding of zircaloys, fuel pellet-cladding interaction etc. in PHWR and void swelling; irradiation creep and helium embrittlement of fuel element structural materials in FBR are discussed along with measures to overcome some of these problems. (author). 15 refs., 9 tabs., 23 figs

History of fast reactor fuel development

Energy Technology Data Exchange (ETDEWEB)

Kittel, J.H. (Argonne National Lab., IL (United States)); Frost, B.R.T. (Argonne National Lab., IL (United States)); Mustelier, J.P. (COGEMA, Velizy-Villacoublay (France)); Bagley, K.Q. (AEA Reactor Services, Risley (United Kingdom)); Crittenden, G.C. (AEA Reactor Services, Dounreay (United Kingdom)); Dievoet, J. van (Belgonucleaire, Brussels (Belgium))

1993-09-01

The first fast breeder eactors, constructed in the 1945-1960 time period, used metallic fuels composed of uranium, plutonium, or their alloys. They were chosen because most existing reactor operating experience had been obtained on metallic fuels and because they provided the highest breeding ratios. Difficulties in obtaining adequate dimensional stability in metallic fuel elements under conditions of high fuel burnup led in the 1960s to the virtual worldwide choice of ceramic fuels. Although ceramic fuels provide lower breeding performance, this objective is no longer an important consideration in most national programs. Mixed uranium and plutonium dioxide became the ceramic fuel that has received the widest use. The more advanced ceramic fuels, mixed uranium and plutonium carbides and nitrides, continue under development. More recently, metal fuel elements of improved design have joined ceramic fuels in achieving goal burnups of 15 to 20 percent. Low-swelling fuel cladding alloys have also been continuously developed to deal with the unexpected problem of void formation in stainless steels subjected to fast neutron irradiation, a phenomenon first observed in the 1960s. (orig.)

Fuel balance in nuclear power with fast reactors without a uranium blanket

International Nuclear Information System (INIS)

Naumov, V.V.; Orlov, V.V.; Smirnov, V.S.

1994-01-01

General aspects related to replacing the uranium blanket of a lead-cooled fast reactor burning uranium-plutonium nitride fuel with a more efficient lead reflector are briefly discussed in the article. A study is very briefly summarized, which showed that a breeding ratio of about 1 and electric power of about 300 MW were achievable. A nuclear fuel balance is performed to estimate the increased consumption of uranium to produce power and the gains achievable by eliminating the uranium blanket. Elimination of the uranium blanket has the advantages of simplifying and improving the fast reactor and eliminating the production of weapons quality plutonium. 3 figs

Occupational safety data and casualty rates for the uranium fuel cycle

International Nuclear Information System (INIS)

O'Donnell, F.R.; Hoy, H.C.

1981-10-01

Occupational casualty (injuries, illnesses, fatalities, and lost workdays) and production data are presented and used to calculate occupational casualty incidence rates for technologies that make up the uranium fuel cycle, including: mining, milling, conversion, and enrichment of uranium; fabrication of reactor fuel; transportation of uranium and fuel elements; generation of electric power; and transmission of electric power. Each technology is treated in a separate chapter. All data sources are referenced. All steps used to calculate normalized occupational casualty incidence rates from the data are presented. Rates given include fatalities, serious cases, and lost workdays per 100 man-years worked, per 10 12 Btu of energy output, and per other appropriate units of output

Science communication from women in nuclear fuel development

International Nuclear Information System (INIS)

Roy, S.B.

2013-01-01

In India, nuclear fuel is required for operating both nuclear research reactors and power reactors. Indian women are extensively involved in nuclear fuel research and production activities. However, the nature and extent of their involvement differs based only on the job required and not on any gender basis. Excluding a few specific safety and security issues, therefore, science and technology communication really does not change according to the gender of the scientist or technologist. Presently in India, nuclear grade uranium metal is required for fuelling research reactors and nuclear grade uranium oxide is being utilized as fuel for power reactors. Hydrometallurgical operations using specific solvents are being used for achieving 'nuclear grade' in both sectors. For production of uranium oxide, purified uranium compounds need to get calcined and reduced for obtaining uranium dioxide of various qualities

Irradiation behavior of experimental miniature uranium silicide fuel plates

International Nuclear Information System (INIS)

Hofman, Gerard L.; Neimark, L.A.; Mattas, R.F.

1983-01-01

Uranium silicides, because of their relatively high uranium density, were selected as candidate dispersion fuels for the higher fuel densities required in the Reduced Enrichment Research and Test Reactor (RERTR) Program. Irradiation experience with this type of fuel, however, was limited to relatively modest fission densities in the bulk form, on the order of 7 x 10 20 cm -3 , far short of he approximately 20 x 10 20 cm -3 goal established for the RERTR Program. The purpose of the irradiation experiments on silicide fuels in the ORR, therefore, was to investigate the intrinsic irradiation behavior of uranium silicide as a dispersion fuel. Of particular interest was the interaction between the silicide particles and the aluminum matrix, the swelling behavior of the silicide particles, and the maximum volume fraction of silicide particles that could be contained in the aluminum matrix. The first group of experimental 'mini' fuel plates have recently reached the program's goal burnup and are in various stages of examination. Although the results to date indicate some limitations, it appears that within the range of parameters examined thus far the uranium silicide dispersion holds promise for satisfying most of the needs of the RERTR Program. The twelve experimental silicide dispersion fuel plates that were irradiated to approximately their goal exposure show the 30-vol % U 3 Si-Al plates to be in a stage of relatively rapid fission-gas-driven swelling at a fission density of 2 x 10 20 cm -3 . This fuel swelling will likely result in unacceptably large plate-thickness increases. The U 3 Si plates appear to be superior in this respect; however, they, too, are starting to move into the rapid fuel-swelling stage. Analysis of the currently available post irradiation data indicates that a 40-vol % dispersed fuel may offer an acceptable margin to the onset of unstable thickness changes at exposures of 2 x 10 21 fission/cm 3 . The interdiffusion between fuel and matrix

Irradiation Testing of TRISO-Coated Particle Fuel in Korea

International Nuclear Information System (INIS)

Kim, Bong Goo; Yeo, Sunghwan; Jeong, Kyung-Chai; Eom, Sung-Ho; Kim, Yeon-Ku; Kim, Woong Ki; Lee, Young Woo; Cho, Moon Sung; Kim, Yong Wan

2014-01-01

In Korea, coated particle fuel is being developed to support development of a VHTR. At the end of March 2014, the first irradiation test in HANARO at KAERI to demonstrate and qualify TRISO-coated particle fuel for use in a VHTR was terminated. This experiment was conducted in an inert gas atmosphere without on-line temperature monitoring and control, or on-line fission product monitoring of the sweep gas. The irradiation device contained two test rods, one has nine fuel compacts and the other five compacts and eight graphite specimens. Each compact contains about 260 TRISO-coated particles. The duration of irradiation testing at HANARO was about 135 full power days from last August 2013. The maximum average power per particle was about 165 mW/particle. The calculated peak burnup of the TRISO-coated fuel was a little less than 4 atom percent. Post-irradiation examination is being carried out at KAERI’s Irradiated Material Examination Facility beginning in September of 2014. This paper describes characteristics of coated particle fuel, the design of the test rod and irradiation device for this coated particle fuel, and discusses the technical results of irradiation testing at HANARO. (author)

Following the electroreduction of uranium dioxide to uranium in LiCl–KCl eutectic in situ using synchrotron radiation

Energy Technology Data Exchange (ETDEWEB)

Brown, L.D.; Abdulaziz, R.; Jervis, R.; Bharath, V.J. [Electrochemical Innovation Lab, Dept. Chemical Engineering, UCL, London WC1E 7JE (United Kingdom); Atwood, R.C.; Reinhard, C.; Connor, L.D. [Diamond Light Source, Harwell Science and Innovation Campus, Didcot, Oxfordshire OX11 0DE (United Kingdom); Simons, S.J.R.; Inman, D.; Brett, D.J.L. [Electrochemical Innovation Lab, Dept. Chemical Engineering, UCL, London WC1E 7JE (United Kingdom); Shearing, P.R., E-mail: p.shearing@ucl.ac.uk [Electrochemical Innovation Lab, Dept. Chemical Engineering, UCL, London WC1E 7JE (United Kingdom)

2015-09-15

Highlights: • We investigated the electroreduction of UO{sub 2} to U in LiCl/KCL eutectic molten salt. • Combined electrochemical measurement and in situ XRD is utilised. • The electroreduction appears to occur in a single, 4-electron-step, process. • No intermediate compounds were observed. - Abstract: The electrochemical reduction of uranium dioxide to metallic uranium has been investigated in lithium chloride–potassium chloride eutectic molten salt. Laboratory based electrochemical studies have been coupled with in situ energy dispersive X-ray diffraction, for the first time, to deduce the reduction pathway. No intermediate phases were identified using the X-ray diffraction before, during or after electroreduction to form α-uranium. This suggests that the electrochemical reduction occurs via a single, 4-electron-step, process. The rate of formation of α-uranium is seen to decrease during electrolysis and could be a result of a build-up of oxygen anions in the molten salt. Slow transport of O{sup 2−} ions away from the UO{sub 2} working electrode could impede the electrochemical reduction.

Development, preparation and characterization of uranium molybdenum alloys for dispersion fuel application

Energy Technology Data Exchange (ETDEWEB)

Sinha, V.P. [Metallic Fuels Division, Bhabha Atomic Research Centre, Mumbai 400085 (India)], E-mail: vedsinha@barc.gov.in; Prasad, G.J.; Hegde, P.V.; Keswani, R.; Basak, C.B.; Pal, S.; Mishra, G.P. [Metallic Fuels Division, Bhabha Atomic Research Centre, Mumbai 400085 (India)

2009-04-03

Most of the research and test reactors worldwide have undergone core conversion from high enriched uranium base fuel to low enriched uranium base fuel under the Reduced Enrichment for Research and Test Reactor (RERTR) program, which was launched in the late 1970s to reduce the risk of nuclear proliferation. To realize this goal, high density uranium compounds and {gamma}-stabilized uranium alloy powder were identified. In Metallic Fuels Division of BARC, R and D efforts are on to develop these high density uranium base alloys. This paper describes the preparation flow sheet for different compositions of Uranium and molybdenum alloys by an innovative powder processing route with uranium and molybdenum metal powders as starting materials. The same composition of U-Mo alloys were also fabricated by conventional method i.e. ingot metallurgy route. The U-Mo alloys prepared by both the methods were then characterized by XRD for phase analysis. The photomicrographs of alloys with different compositions prepared by powder metallurgy and ingot metallurgy routes are also included in the paper. The paper also covers the comparison of properties of the alloys prepared by powder metallurgy and ingot metallurgy routes.

Development, preparation and characterization of uranium molybdenum alloys for dispersion fuel application

International Nuclear Information System (INIS)

Sinha, V.P.; Prasad, G.J.; Hegde, P.V.; Keswani, R.; Basak, C.B.; Pal, S.; Mishra, G.P.

2009-01-01

Most of the research and test reactors worldwide have undergone core conversion from high enriched uranium base fuel to low enriched uranium base fuel under the Reduced Enrichment for Research and Test Reactor (RERTR) program, which was launched in the late 1970s to reduce the risk of nuclear proliferation. To realize this goal, high density uranium compounds and γ-stabilized uranium alloy powder were identified. In Metallic Fuels Division of BARC, R and D efforts are on to develop these high density uranium base alloys. This paper describes the preparation flow sheet for different compositions of Uranium and molybdenum alloys by an innovative powder processing route with uranium and molybdenum metal powders as starting materials. The same composition of U-Mo alloys were also fabricated by conventional method i.e. ingot metallurgy route. The U-Mo alloys prepared by both the methods were then characterized by XRD for phase analysis. The photomicrographs of alloys with different compositions prepared by powder metallurgy and ingot metallurgy routes are also included in the paper. The paper also covers the comparison of properties of the alloys prepared by powder metallurgy and ingot metallurgy routes

Studies on the sintering behaviour of uranium dioxide powder compacts

International Nuclear Information System (INIS)

Das, P.; Chowdhury, R.

1988-01-01

Uranium dioxide fuel pellets are normally made from their precursor ammonium diuranate, followed by calcination, subsequent reduction to sinterable grade powders and a post operation treatment of pressing and sintering. The low temperature calcined powders, usually exhibiting non-crystalline behaviour (under X-ray diffraction studies) progressively transforms into a crystalline variety on subsequent heat treatment at higher temperature. It is observed however that powders calcined between 800 to 900 0 C exhibit enhanced densification behaviour when sintered at higher temperatures. The isothermal shrinkage versus time plot of the sintered compacts are well described by a hyperbolic relationship which takes care of the observed shrinkage (λ) as caused due to a cumulative effect from the initial sintering of the powder compacts at zero time (α) and that caused due to the structural transformation from a non-crystalline modification with increased thermal treatment (β). The derived equation is a modification of the sintering mechanism of the viscous flow type proposed by Frenkel, involving sintering of an amorphous phase, the viscosity of the latter is presumed to increase with increasing thermal treatment to assume the final modified form as λ=t/(α+βt), where t = time, λ = shrinkage and α and β are the unknown parameters. (orig.)

Impact on burnup performance of coated particle fuel design in pebble bed reactor with ROX fuel

International Nuclear Information System (INIS)

Ho, Hai Quan; Obara, Toru

2015-01-01

The pebble bed reactor (PBR), a kind of high-temperature gas-cooled reactor (HTGR), is expected to be among the next generation of nuclear reactors as it has excellent passive safety features, as well as online refueling and high thermal efficiency. Rock-like oxide (ROX) fuel has been studied at the Japan Atomic Energy Agency (JAEA) as a new once-through type fuel concept. Rock-like oxide used as fuel in a PBR can be expected to achieve high burnup and improve chemical stabilities. In the once-through fuel concept, the main challenge is to achieve as high a burnup as possible without failure of the spent fuel. The purpose of this study was to investigate the impact on burnup performance of different coated fuel particle (CFP) designs in a PBR with ROX fuel. In the study, the AGR-1 Coated Particle design and Deep-Burn Coated Particle design were used to make the burnup performance comparison. Criticality and core burnup calculations were performed by MCPBR code using the JENDL-4.0 library. Results at equilibrium showed that the two reactors utilizing AGR-1 Coated Particle and Deep-Burn Coated Particle designs could be critical with almost the same multiplication factor k eff . However, the power peaking factor and maximum power per fuel ball in the AGR-1 coated particle design was lower than that of Deep-Burn coated particle design. The AGR-1 design also showed an advantage in fissions per initial fissile atoms (FIFA); the AGR-1 coated particle design produced a higher FIFA than the Deep-Burn coated particle design. These results suggest that the difference in coated particle fuel design can have an effect on the burnup performance in ROX fuel. (author)

gamma-ray spectra measurements for long cooled MOX spent fuels

International Nuclear Information System (INIS)

Murakami, Kiyonobu; Kobayashi, Iwao

1993-09-01

Gamma-ray spectra of spent fuels have important informations in the estimation of burnup rate, concentration of fission products, cooling time and etc. which are required in the fuel loading control of reactors and special nuclear materials accountancy from the view point of safe guard. Although, some available data are given about uranium dioxide fuels, few data are given about uranium and plutonium dioxide mixtures (MOX fuels). Especially, there is few data about MOX fuels which are irradiated in thermal reactors and cooled more than ten years. Gamma-ray spectra are measured for PuO 2 -UO 2 fuel rods (IFA-159, IFA-160) which are irradiated at HBWR in Norway up to 9,420 and 5,340MWd/t respectively. Gamma-ray spectra had been measured about the two fuels ten years ago at the spent fuel pond of Japan Demonstration Reactor (JPDR). The objectives of this measurement is to know how decayed the gamma-ray spectra in these ten years and some fission products are there which are effective to estimate burnup rate of spent MOX fuels. (author)

Sodium-cooled Fast Reactor Cores using Uranium-Free Metallic Fuels for Maximizing TRU Support Ratio

International Nuclear Information System (INIS)

You, WuSeung; Hong, Ser Gi

2014-01-01

The depleted uranium plays important roles in the SFR burner cores because it substantially contributes to the inherent safety of the core through the negative Doppler coefficient and large delayed neutron. However, the use of depleted uranium as a diluent nuclide leads to a limited value of TRU support ratio due to the generation of TRUs through the breeding. In this paper, we designed sodium cooled fast reactor (SFR) cores having uranium-free fuels 3,4 for maximization of TRU consumption rate. However, the uranium-free fuelled burner cores can be penalized by unacceptably small values of the Doppler coefficient and small delayed neutron fraction. In this work, metallic fuels of TRU-(W or Ni)-Zr are considered to improve the performances of the uranium-free cores. The objective of this work is to consistently compare the neutronic performances of uranium-free sodium cooled fast reactor cores having TRU-Zr metallic fuels added with Ni or W and also to clarify what are the problematic features to be resolved. In this paper, a consistent comparative study of 400MWe sodium cooled burner cores having uranium-based fuels and uranium-free fuels was done to analyze the relative core neutronic features. Also, we proposed a uranium-free metallic fuel based on Nickel. From the results, it is found that tungsten-based uranium-free metallic fuel gives large negative Doppler coefficient due to high resonance of tungsten isotopes but this core has large sodium void worth and small effective delayed neutron fraction while the nickel-based uranium-free metallic fuelled core has less negative Doppler coefficient but smaller sodium void worth and larger effective delayed neutron fraction than the tungsten-based one. On the other hand, the core having TRU-Zr has very high burnup reactivity swing which may be problematic in compensating it using control rods and the least negative Doppler coefficient

Detection of carbon dioxide in the gases evolved during the hot extraction determination of hydrogen in uranium ingots

International Nuclear Information System (INIS)

Jursik, M.L.; Pope, J.D.

1977-08-01

The hot extraction method was used at the National Lead Company of Ohio to determine hydrogen in uranium metal at the 2 ppM level. The volume of gas evolved from the heated sample was assumed to be hydrogen. When a liquid nitrogen trap was placed into the system the hydrogen values were reduced 5 to 10%. The gas retained by the nitrogen trap was identified by mass spectrometry as predominantly carbon dioxide. Low hydrogen values were observed only when the nitrogen trap was used in the analysis of high-carbon (300 to 600 ppM) uranium from NLO production ingots. However, hydrogen values for low-carbon (30 to 50 ppM) uranium were unaffected by the nitrogen trap. The formation of carbon dioxide appears to be associated with the carbon content of the uranium metal. Comparisons of hydrogen values obtained with the hot extraction method and with an inert fusion--thermal conductivity method are also presented. 3 tables, 4 figures

Studies on O/M ratio determination in uranium oxide, plutonium oxide and uranium-plutonium mixed oxide

International Nuclear Information System (INIS)

Sampath, S.; Chawla, K.L.

1975-01-01

Thermogravimetric studies were carried out in unsintered and sintered samples of uranium oxide, plutonium oxide and uranium-plutonium mixed oxide under different atmospheric conditions (air, argon and moist argon/hydrogen). Moisture loss was found to occur below 200 0 C for uranium dioxide samples, upto 700 0 C for sintered plutonium dioxide and negligible for sintered samples. The O/M ratios for non-stoichiometric uranium dioxide (sintered and unsintered), plutonium dioxide and mixed uranium and plutonium oxides (sintered) could be obtained with a precision of +- 0.002. Two reference states UOsub(2.000) and UOsub(2.656) were obtained for uranium dioxide and the reference state MOsub(2.000) was used for other cases. For unsintered plutonium dioxide samples, accurate O/M ratios could not be obtained of overlap of moisture loss with oxygen loss/gain. (author)

Automation of potentiometric titration for the determination of uranium in nuclear fuel materials

International Nuclear Information System (INIS)

Kelkar, Anoop; Pandey, Ashish; Kapoor, Y.S.; Kumar, Manish; Singh, Mamta; Fulzele, Ajeet; Prakash, Amrit; Afzal, Mohd; Panakkal, J.P.

2010-01-01

Advanced Fuel Fabrication Facility is fabricating various types of mixed oxide fuels, namely for PHWR, BWR, FBTR and PFBR. Precise determination of uranium in MOX fuel sample is important to get desired burn up in the reactor. The modified Davies and Gray method is routinely used for the potentiometric titration of uranium

Fuel particle coating data. [Detailed information on coating runs at Los Alamos Scientific Laboratory

Energy Technology Data Exchange (ETDEWEB)

Hollabaugh, C.M.; Wagner, P.; Wahman, L.A.; White, R.W.

1977-01-01

Development of coating on nuclear fuel particles for the High-Temperature Fuels Technology program at the Los Alamos Scientific Laboratory included process studies for low-density porous and high-density isotropic carbon coats, and for ZrC and ''alloy'' C/ZrC coats. This report documents the data generated by these studies.

Isotopic composition and radiological properties of uranium in selected fuel cycles

International Nuclear Information System (INIS)

Fleischman, R.M.; Liikala, R.C.

1975-04-01

Three major topic areas are discussed: First, the properties of the uranium isotopes are defined relative to their respective roles in the nuclear fuel cycle. Secondly, the most predominant fuel cycles expected in the U. S. are described. These are the Light Water Reactor (LWR), High Temperature Gas Cooled Reactor (HTGR), and Liquid Metal Fast Breeder Reactor (LMFBR) fuel cycles. The isotopic compositions of uranium and plutonium fuels expected for these fuel cycles are given in some detail. Finally the various waste streams from these fuel cycles are discussed in terms of their relative toxicity. Emphasis is given to the high level waste streams from reprocessing of spent fuel. Wastes from the various fuel cycles are compared based on projected growth patterns for nuclear power and its various components. (U.S.)

A Preliminary Study on the Reuse of the Recovered Uranium from the Spent CANDU Fuel Using Pyroprocessing

International Nuclear Information System (INIS)

Park, C. J.; Na, S. H.; Yang, J. H.; Kang, K. H.; Lee, J. W.

2009-01-01

During the pyroprocessing, most of the uranium is gathered in metallic form around a solid cathode during an electro-refining process, which is composed of about 94 weight percent of the spent fuel. In the previous study, a feasibility study has been done to reuse the recovered uranium for the CANDU reactor fuel following the traditional DUPIC (direct use of spent pressurized water reactor fuel into CANDU reactor) fuel fabrication process. However, the weight percent of U-235 in the recovered uranium is about 1 wt% and it is sufficiently re-utilized in a heavy water reactor which uses a natural uranium fuel. The reuse of recovered uranium will bring not only a huge economic profit and saving of uranium resources but also an alleviation of the burden on the management and the disposal of the spent fuel. The research on recycling of recovered uranium was carried out 10 years ago and most of the recovered uranium was assumed to be imported from abroad at that time. The preliminary results showed there is the sufficient possibility to recycle recovered uranium in terms of a reactor's characteristics as well as the fuel performance. However, the spent CANDU fuel is another issue in the storage and disposal problem. At present, most countries are considering that the spent CANDU fuel is disposed directly due to the low enrichment (∼0.5 wt%) of the discharge fissile content and lots of fission products. If mixing the spent CANDU fuel and the spent PWR fuel, the estimated uranium fissile enrichment will be about 0.6 wt% ∼ 1.0 wt% depending on the mixing ratio, which is sufficiently reusable in a CANDU reactor. Therefore, this paper deals with a feasibility study on the recovered uranium of the mixed spent fuel from the pyroprocessing. With the various mixing ratios between the PWR spent fuel and the CANDU spent fuel, a reactor characteristics including the safety parameters of the CANDU reactor was evaluated

Analysis of the Reuse of Uranium Recovered from the Reprocessing of Commercial LWR Spent Fuel

International Nuclear Information System (INIS)

DelCul, Guillermo D.; Trowbridge, Lee D.; Renier, John-Paul; Ellis, Ronald James; Williams, Kent Alan; Spencer, Barry B.; Collins, Emory D.

2009-01-01

This report provides an analysis of the factors involved in the reuse of uranium recovered from commercial light-water-reactor (LWR) spent fuels (1) by reenrichment and recycling as fuel to LWRs and/or (2) by recycling directly as fuel to heavy-water-reactors (HWRs), such as the CANDU (registered trade name for the Canadian Deuterium Uranium Reactor). Reuse is an attractive alternative to the current Advanced Fuel Cycle Initiative (AFCI) Global Nuclear Energy Partnership (GNEP) baseline plan, which stores the reprocessed uranium (RU) for an uncertain future or attempts to dispose of it as 'greater-than-Class C' waste. Considering that the open fuel cycle currently deployed in the United States already creates a huge excess quantity of depleted uranium, the closed fuel cycle should enable the recycle of the major components of spent fuel, such as the uranium and the hazardous, long-lived transuranic (TRU) actinides, as well as the managed disposal of fission product wastes. Compared with the GNEP baseline scenario, the reuse of RU in the uranium fuel cycle has a number of potential advantages: (1) avoidance of purchase costs of 11-20% of the natural uranium feed; (2) avoidance of disposal costs for a large majority of the volume of spent fuel that is reprocessed; (3) avoidance of disposal costs for a portion of the depleted uranium from the enrichment step; (4) depending on the 235 U assay of the RU, possible avoidance of separative work costs; and (5) a significant increase in the production of 238 Pu due to the presence of 236 U, which benefits somewhat the transmutation value of the plutonium and also provides some proliferation resistance

Study of rare gases behavior in uranium dioxide: diffusion and bubble nucleation and growth mechanisms

International Nuclear Information System (INIS)

Michel, A.

2011-01-01

During in-reactor irradiation of the nuclear fuel, fission gases, mainly xenon and krypton, are generated that are subject to several phenomena: diffusion and precipitation. These phenomena can have adverse consequences on the fuel physical and chemical properties and its in-reactor behavior. The purpose of this work is to better understand the behavior of fission gases by identifying diffusion, bubble nucleation and growth mechanisms. To do this, studies involving separate effects have been established coupling ion irradiations/implantations with fine characterizations on Large Scale Facilities. The influence of several parameters such as gas type, concentration and temperature has been identified separately. Interpretation of the Thermal Desorption Spectrometry (TDS) measurements has enabled us to determine xenon and krypton diffusion coefficients in uranium dioxide. A heterogeneous nucleation mechanism on defects was determined by means of experiments on the JANNuS platform in Orsay that consists of a coupling of an implantor, an accelerator and a Transmission Electron Microscope (TEM). Finally, TEM and X-ray Absorption Spectroscopy characterizations of implanted and annealed samples put in relieve a bubble growth mechanism by atoms and vacancies capture. (author) [fr

Sustainable and safe energy supply with seawater uranium fueled HTGR and its economy

International Nuclear Information System (INIS)

Fukaya, Y.; Goto, M.

2017-01-01

Highlights: • We discussed uranium resources with an energy security perspective. • We concluded seawater uranium is preferable for sustainability and energy security. • We evaluated electricity generation cost of seawater uranium fueled HTGR. • We concluded electricity generation with seawater uranium is reasonable. - Abstract: Sustainable and safe energy supply with High Temperature Gas-cooled Reactor (HTGR) fueled by uranium from seawater have been investigated and discussed. From the view point of safety feature of self-regulation with thermal reactor of HTGR, the uranium resources should be inexhaustible. The seawater uranium is expected to be alternative resources to conventional resources because it exists so much in seawater as a solute. It is said that 4.5 billion tons of uranium is dissolved in the seawater, which corresponds to a consumption of approximately 72 thousand years. Moreover, a thousand times of the amount of 4.5 trillion tU of uranium, which corresponds to the consumption of 72 million years, also is included in the rock on the surface of the sea floor, and that is also recoverable as seawater uranium because uranium in seawater is in an equilibrium state with that. In other words, the uranium from seawater is almost inexhaustible natural resource. However, the recovery cost with current technology is still expensive compared with that of conventional uranium. Then, we assessed the effect of increase in uranium purchase cost on the entire electricity generation cost. In this study, the economy of electricity generation of cost of a commercial HTGR was evaluated with conventional uranium and seawater uranium. Compared with ordinary LWR using conventional uranium, HTGR can generate electricity cheaply because of small volume of simple direct gas turbine system compared with water and steam systems of LWR, rationalization by modularizing, and high thermal efficiency, even if fueled by seawater uranium. It is concluded that the HTGR

21 CFR 175.390 - Zinc-silicon dioxide matrix coatings.

Science.gov (United States)

2010-04-01

...) (using 20 percent alcohol as the solvent when the type of food contains approximately 20 percent alcohol... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Zinc-silicon dioxide matrix coatings. 175.390 Section 175.390 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES...

Ceramography of Irradiated tristructural isotropic (TRISO) Fuel from the AGR-2 Experiment

Energy Technology Data Exchange (ETDEWEB)

Rice, Francine Joyce [Idaho National Lab. (INL), Idaho Falls, ID (United States); Stempien, John Dennis [Idaho National Lab. (INL), Idaho Falls, ID (United States)

2016-09-01

Ceramography was performed on cross sections from four tristructural isotropic (TRISO) coated particle fuel compacts taken from the AGR-2 experiment, which was irradiated between June 2010 and October 2013 in the Advanced Test Reactor (ATR). The fuel compacts examined in this study contained TRISO-coated particles with either uranium oxide (UO2) kernels or uranium oxide/uranium carbide (UCO) kernels that were irradiated to final burnup values between 9.0 and 11.1% FIMA. These examinations are intended to explore kernel and coating morphology evolution during irradiation. This includes kernel porosity, swelling, and migration, and irradiation-induced coating fracture and separation. Variations in behavior within a specific cross section, which could be related to temperature or burnup gradients within the fuel compact, are also explored. The criteria for categorizing post-irradiation particle morphologies developed for AGR-1 ceramographic exams, was applied to the particles in the AGR-2 compacts particles examined. Results are compared with similar investigations performed as part of the earlier AGR-1 irradiation experiment. This paper presents the results of the AGR-2 examinations and discusses the key implications for fuel irradiation performance.