WorldWideScience

Sample records for cerium hydrides

  1. Probing the cerium/cerium hydride interface using nanoindentation

    Energy Technology Data Exchange (ETDEWEB)

    Brierley, Martin, E-mail: martin.brierley@awe.co.uk [Atomic Weapons Establishment, Aldermaston, Berkshire RG7 4PR (United Kingdom); University of Manchester, Manchester M13 9PL (United Kingdom); Knowles, John, E-mail: john.knowles@awe.co.uk [Atomic Weapons Establishment, Aldermaston, Berkshire RG7 4PR (United Kingdom)

    2015-10-05

    Highlights: • A disparity exists between the minimum energy and actual shape of a cerium hydride. • Cerium hydride is found to be harder than cerium metal by a ratio of 1.7:1. • A zone of material under compressive stress was identified surrounding the hydride. • No distribution of hardness was apparent within the hydride. - Abstract: A cerium hydride site was sectioned and the mechanical properties of the exposed phases (cerium metal, cerium hydride, oxidised cerium hydride) were measured using nanoindentation. An interfacial region under compressive stress was observed in the cerium metal surrounding a surface hydride that formed as a consequence of strain energy generated by the volume expansion associated with precipitation of the hydride phase.

  2. Probing the cerium/cerium hydride interface using nanoindentation

    International Nuclear Information System (INIS)

    Highlights: • A disparity exists between the minimum energy and actual shape of a cerium hydride. • Cerium hydride is found to be harder than cerium metal by a ratio of 1.7:1. • A zone of material under compressive stress was identified surrounding the hydride. • No distribution of hardness was apparent within the hydride. - Abstract: A cerium hydride site was sectioned and the mechanical properties of the exposed phases (cerium metal, cerium hydride, oxidised cerium hydride) were measured using nanoindentation. An interfacial region under compressive stress was observed in the cerium metal surrounding a surface hydride that formed as a consequence of strain energy generated by the volume expansion associated with precipitation of the hydride phase

  3. Investigation into the lattice dynamics of cerium hydride by inelastic neutron scattering

    International Nuclear Information System (INIS)

    The inelastic neutron scattering on polycrystalline CeHsub(1.98) and CeHsub(2,72) was measured with a neutron time-of-flight spectrometer. The experimentally obtained time-of-flight distributions of the scattered neutrons were analyzed considering the spectrometer resolution according to the Born- von Karman theory of lattice dynamics assuming central forces between the lattice atoms. One could determine numerical values of the force constants for cerium dihydride (CaF2 structure), with which the lattice dynamics model showed good agreement in the measured neutron time-of-flight distributions for CeHsub(1.90) as well as in the temperature dependene of the measured specific heat on CeHsub(2.00). For cerium trihydride (BiF3 sturcture), the measured time-of-flight distributions could only be qualitatively interpreted for CeHsub(2.72) within the framework of the lattice dynamics model used. Two numerical sets of the force constants were discussed. (orig./HPOE)

  4. Interstellar Hydrides

    CERN Document Server

    Gerin, Maryvonne; Goicoechea, Javier R

    2016-01-01

    Interstellar hydrides -- that is, molecules containing a single heavy element atom with one or more hydrogen atoms -- were among the first molecules detected outside the solar system. They lie at the root of interstellar chemistry, being among the first species to form in initially-atomic gas, along with molecular hydrogen and its associated ions. Because the chemical pathways leading to the formation of interstellar hydrides are relatively simple, the analysis of the observed abundances is relatively straightforward and provides key information about the environments where hydrides are found. Recent years have seen rapid progress in our understanding of interstellar hydrides, thanks largely to far-IR and submillimeter observations performed with the Herschel Space Observatory. In this review, we will discuss observations of interstellar hydrides, along with the advanced modeling approaches that have been used to interpret them, and the unique information that has thereby been obtained.

  5. Reaction chemistry of cerium

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-01-01

    It is truly ironic that a synthetic organic chemist likely has far greater knowledge of the reaction chemistry of cerium(IV) than an inorganic colleague. Cerium(IV) reagents have long since been employed as oxidants in effecting a wide variety of organic transformations. Conversely, prior to the late 1980s, the number of well characterized cerium(IV) complexes did not extend past a handful of known species. Though in many other areas, interest in the molecular chemistry of the 4f-elements has undergone an explosive growth over the last twenty years, the chemistry of cerium(IV) has for the most part been overlooked. This report describes reactions of cerium complexes and structure.

  6. Hydride compressor

    Science.gov (United States)

    Powell, James R.; Salzano, Francis J.

    1978-01-01

    Method of producing high energy pressurized gas working fluid power from a low energy, low temperature heat source, wherein the compression energy is gained by using the low energy heat source to desorb hydrogen gas from a metal hydride bed and the desorbed hydrogen for producing power is recycled to the bed, where it is re-adsorbed, with the recycling being powered by the low energy heat source. In one embodiment, the adsorption-desorption cycle provides a chemical compressor that is powered by the low energy heat source, and the compressor is connected to a regenerative gas turbine having a high energy, high temperature heat source with the recycling being powered by the low energy heat source.

  7. Synthesis of ruthenium hydride

    Science.gov (United States)

    Kuzovnikov, M. A.; Tkacz, M.

    2016-02-01

    Ruthenium hydride was synthesized at a hydrogen pressure of about 14 GPa in a diamond-anvil cell. Energy-dispersive x-ray diffraction was used to monitor the ruthenium crystal structure as a function of hydrogen pressure up to 30 GPa. The hydride formation was accompanied by phase transition from the original hcp structure of the pristine metal to the fcc structure. Our results confirmed the theoretical prediction of ruthenium hydride formation under hydrogen pressure. The standard Gibbs free energy of the ruthenium hydride formation reaction was calculated assuming the pressure of decomposition as the equilibrium pressure.

  8. Hydrated cerium(3) vanadates

    International Nuclear Information System (INIS)

    It has been ascertained by the methods of chemical, thermal and X-ray phase analyses, IR spectroscopy that in the system LiVO3-Ce(NO3)3-HNO3-LiOH-H2O in equilibrium conditions the following compounds are precipitated: cerium dodecavanadate Ce2(V12O31)3·3nH2O, where 11.0 5O13)2·nH2O, where 6.5 2V10O28·19H2O; vanadates Ce(VO3)3·4H2O and CeVO4·H2O. Cerium orthovanadate is crystallized in tetragonal crystal system with zircon structure and crystal lattice parameters as follows: a=7.3726(14) and c=6.4939(23) A

  9. Hysteresis phenomenon and huge isotope effect in hydrogenation cycles of some cerium-containing LaNi5-type compounds

    International Nuclear Information System (INIS)

    The huge hysteresis effect and the isotope effect, two effects that accompany the hydrogen absorbing process of cerium containing LaHi5-type compound were studied. The hysteresis effect was studied on compounds of the type (Lasub(0.5)Cesub(0.5))Nisub(5-x)Cosuh(x) and their hydrides, for 0 5 compounds display very large hysteresis effect in the course of a hydrogenation cycle. The addition of cobalt markedly affects the absorption pressure plateau which reverts to normal value at x = 1, practically eliminating the hysteresis effect. The results indicate that the relevant absorption pressure plateau and the resulting hysteresis effect are due to the presence of cerium atoms and to the formation of the expanded Hsup(I) LaNi5-type hydride. The formation of this hydride phase favours the reversion of cerium to the trivalent state. The substitution of 20% of the nickel atoms by cobalt atoms suppresses the formation of the Hsup(I) hydride which is replaced by tOe less expanded Hsup(II) hydride. The Hsup(II) hydride does not display anomalous hysteresis effect. Similar results were obtained for MmNisub(5-x)Cosub(x) (Mm = mischmetal). The isotope effect was studied on the compound (Lasub(0.4)Cesub(0.6))Ni5. The pressure-composition isotherms were determined both for hydrogen and deuterium for different working temperatures. A huge temperature-dependent isotope effect with cross-over occurring below room temperature was observed. The enthalpy and entropy differences between the hydride and the deuteride were calculated and found to be more negative in the deuteride both for the absorption and desorption pressures

  10. Metal Hydrides for Rechargeable Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Valoeen, Lars Ole

    2000-03-01

    Rechargeable battery systems are paramount in the power supply of modern electronic and electromechanical equipment. For the time being, the most promising secondary battery systems for the future are the lithium-ion and the nickel metal hydride (NiMH) batteries. In this thesis, metal hydrides and their properties are described with the aim of characterizing and improving those. The thesis has a special focus on the AB{sub 5} type hydrogen storage alloys, where A is a rare earth metal like lanthanum, or more commonly misch metal, which is a mixture of rare earth metals, mainly lanthanum, cerium, neodymium and praseodymium. B is a transition metal, mainly nickel, commonly with additions of aluminium, cobalt, and manganese. The misch metal composition was found to be very important for the geometry of the unit cell in AB{sub 5} type alloys, and consequently the equilibrium pressure of hydrogen in these types of alloys. The A site substitution of lanthanum by misch metal did not decrease the surface catalytic properties of AB{sub 5} type alloys. B-site substitution of nickel with other transition elements, however, substantially reduced the catalytic activity of the alloy. If the internal pressure within the electrochemical test cell was increased using inert argon gas, a considerable increase in the high rate charge/discharge performance of LaNi{sub 5} was observed. An increased internal pressure would enable the utilisation of alloys with a high hydrogen equivalent pressure in batteries. Such alloys often have favourable kinetics and high hydrogen diffusion rates and thus have a potential for improving the high current discharge rates in metal hydride batteries. The kinetic properties of metal hydride electrodes were found to improve throughout their lifetime. The activation properties were found highly dependent on the charge/discharge current. Fewer charge/discharge cycles were needed to activate the electrodes if a small current was used instead of a higher

  11. Thermodynamic properties of cerium oxide

    International Nuclear Information System (INIS)

    Thermodynamic properties of cerium oxides in the CeO2-CeO1.5 composition range are studied. For this purpose method of electromotive force with solid electrolyte is used, equilibrium constants of reduction of cerium oxides by hydrogen are measured. Necessity of using atmosphere of argon or purified nitrogen to work with pyrophoric cerium oxides is stressed. The obtained results and the earlier known literary data on CeO2 and Ce2O3 thermodynamic properties are tabulated. 14 refs.; 5 tabs

  12. Hydrolysis of lithium hydride

    International Nuclear Information System (INIS)

    Due to its high hydrogen density and unique nuclear chemistry, lithium hydride, in all its isotopic forms, has an unsurpassed place in modem nuclear weapons. The hydrolysis of the material, and the outgassing of hydrogen from the bulk, are crucial to the performance of the material in service. This thesis describes research conducted at AWE Aldermaston, UK, to examine the hydrolysis and hydrogen outgassing from the bulk material, with the aim of ultimately developing the kinetics 8c mechanisms responsible. The basic chemistry is of great interest, especially the reaction with water. This reaction, whilst being fairly extensively studied in the past, has not been conclusively described with an accepted mechanism and associated kinetics. The last significant UK work on the topic was by Imperial College, London, under contract to AW(R)E in the late 1960s. This thesis describes the development of: (i) a solid state NMR spectroscopy technique to examine semi-quantitatively the surface of bulk lithium hydride for its chemical composition, and (ii) a dedicated lithium hydride inert atmosphere gravimetric analysis glove box to study the hydride/water reaction. Solid State NMR Spectroscopy has been utilised for the first time to probe the hydride/hydroxide ratio of partially hydrolysed lithium hydride. 6Li chemical shifts have been established for species of interest and extremely long, up to 17 hours, T1 relaxation times have been measured for 6Li hydride and hydroxide. A method for semi-quantitatively determining the hydroxide/hydride composition of a partially reacted sample has been developed, based on a 'dual-scan' technique using one short and one long pulse sequence. Gravimetric analysis has been developed for lithium hydride/humidity studies. This facility fully contains gravimetric analysis within an argon glove box, with the ability to control the sample atmosphere from room temperature to 60 deg C and from 0.5 to 40 percent relative humidity. The hydrolysis of

  13. Lightweight hydride storage materials

    Energy Technology Data Exchange (ETDEWEB)

    Thomas, G.J.; Guthrie, S.E.; Bauer, W. [Sandia National Labs., Livermore, CA (United States)

    1995-09-01

    The need for lightweight hydrides in vehicular applications has prompted considerable research into the use of magnesium and its alloys. Although this earlier work has provided some improved performance in operating temperature and pressure, substantial improvements are needed before these materials will significantly enhance the performance of an engineered system on a vehicle. We are extending the work of previous investigators on Mg alloys to reduce the operating temperature and hydride heat of formation in light weight materials. Two important results will be discussed in this paper: (1) a promising new alloy hydride was found which has better pressure-temperature characteristics than any previous Mg alloy and, (2) a new fabrication process for existing Mg alloys was developed and demonstrated. The new alloy hydride is composed of magnesium, aluminum and nickel. It has an equilibrium hydrogen overpressure of 1.3 atm. at 200{degrees}C and a storage capacity between 3 and 4 wt.% hydrogen. A hydrogen release rate of approximately 5 x 10{sup -4} moles-H{sub 2}/gm-min was measured at 200{degrees}C. The hydride heat of formation was found to be 13.5 - 14 kcal/mole-H{sub 2}, somewhat lower than Mg{sub 2}Ni. The new fabrication method takes advantage of the high vapor transport of magnesium. It was found that Mg{sub 2}Ni produced by our low temperature process was better than conventional materials because it was single phase (no Mg phase) and could be fabricated with very small particle sizes. Hydride measurements on this material showed faster kinetic response than conventional material. The technique could potentially be applied to in-situ hydride bed fabrication with improved packing density, release kinetics, thermal properties and mechanical stability.

  14. Conference 'Chemistry of hydrides' Proceedings

    International Nuclear Information System (INIS)

    This collection of thesis of conference of Chemistry hydrides presents the results of investigations concerning of base questions of chemistry of nonorganic hydrides, including synthesis questions, studying of physical and chemical properties, thermodynamics, analytical chemistry, investigation of structure, equilibriums in the systems of metal-hydrogen, behaviour of nonorganic hydrides in non-water mediums and applying investigations in the chemistry area and technology of nonorganic hydrides

  15. Preparation of cerium halide solvate complexes

    Science.gov (United States)

    Vasudevan, Kalyan V; Smith, Nickolaus A; Gordon, John C; McKigney, Edward A; Muenchaussen, Ross E

    2013-08-06

    Crystals of a solvated cerium(III) halide solvate complex resulted from a process of forming a paste of a cerium(III) halide in an ionic liquid, adding a solvent to the paste, removing any undissolved solid, and then cooling the liquid phase. Diffusing a solvent vapor into the liquid phase also resulted in crystals of a solvated cerium(III) halide complex.

  16. Valence instabilities in cerium intermetallics

    International Nuclear Information System (INIS)

    The primary purpose of this investigation was to study the magnetic behaviour of cerium in intermetallic compounds, that show an IV behaviour, e.g. CeSn3. In the progress of the investigations, it became of interest to study the effect of changes in the lattice of the IV compound by substituting La or Y for Ce, thus constituting the Cesub(1-x)Lasub(x)Sn3 and Cesub(1-x)Ysub(x)Sn3 quasibinary systems. A second purpose was to examine the possibility of introducing instabilities in the valency of a trivalent intermetallic cerium compound: CeIn3, also by La and Y-substitutions in the lattice. Measurements on the resulting Cesub(1-x)Lasub(x)In3 and Cesub(1-x)Ysub(x)In3 quasibinaries are described. A third purpose was to study the (gradual) transition from a trivalent cerium compound into an IV cerium compound. This was done by examining the magnetic properties of the CeInsub(x)Snsub(3-x) and CePbsub(x)Snsub(3-x) systems. Finally a new possibility was investigated: that of the occurrence of IV behaviour in CeSi2, CeSi, and in CeGa2. (Auth.)

  17. Metal hydride actuation device

    International Nuclear Information System (INIS)

    A self-recocking actuation device is disclosed. One possible use for it is in conjunction with a pneumatic fire protection system. This invention employs the process known as occlusion to store large amounts of gas in a small volume. Metal hydrides in a chamber are used to store hydrogen in the disclosed preferred embodiment. Upon the application of heat-from a heat source like a resistance heater-the charged metal hydride releases its hydrogen (H2) in a chamber having only one exit opening which empties into a sealed bellows. This bellows contacts a piston located in another chamber wherein a biased resetting spring is provided to normally maintain the piston in contact with the bellows. As the pressure from the H2 gas builds up, it overcomes the biased spring to move it and the piston along with an associated pin or other actuator. If used to actuate a pneumatic fire protection system, the pin or actuator at the downward side of its stroke in turn, may puncture a shearable diaphragm or in some other way releases the contents of a container containing a second gas, like nitrogen (N2), which is then released from a second exit port in a different chamber to charge the fire protection system. Recocking of the piston begins as the heating of the metal hydride ceases. As cooling takes place the hydrogen is absorbed to reenter the hydride to decrease the gas pressure supplied. The piston's biased resetting spring then recocks the piston to its original position

  18. Air and metal hydride battery

    Energy Technology Data Exchange (ETDEWEB)

    Lampinen, M.; Noponen, T. [Helsinki Univ. of Technology, Otaniemi (Finland). Lab. of Applied Thermodynamics

    1998-12-31

    The main goal of the air and metal hydride battery project was to enhance the performance and manufacturing technology of both electrodes to such a degree that an air-metal hydride battery could become a commercially and technically competitive power source for electric vehicles. By the end of the project it was possible to demonstrate the very first prototype of the air-metal hydride battery at EV scale, achieving all the required design parameters. (orig.)

  19. Materials engineering of metal hydrides

    International Nuclear Information System (INIS)

    Intermetallic hydrides of the AB5 type have enthalpies in the range valid for chemical heat pumps. A scheme for manufacturing hydrides with optimal properties for a chemical heat pump is described, using LaNi/sub 5-x/Al/sub x/ and ZrV/sub 2x/Cr/sub x as examples. The Laves-phase ternary hydrides appear to be good candidates for gettering hydrogen in the Tokamak Fusion Test Reactor

  20. Improvements in or relating to cerium compounds

    International Nuclear Information System (INIS)

    A process for the preparation of a dispersible cerium compound comprises heating a substantially dry cerium (IV) oxide hydrate in the presence of a deaggregating agent to cause deaggregation of aggregated crystallites in the cerium (IV) oxide hydrate and produce a dry dispersible cerium compound. The deaggregating agent is an acid species e.g. NO3-, Cl- or ClO4-. The dry dispersible product may be mixed with an aqueous medium to form a colloidal dispersion and if the dispersion is allowed to dry, a gel. (author)

  1. Radiative lifetimes of neutral cerium

    International Nuclear Information System (INIS)

    Radiative lifetimes, accurate to ±5%, have been measured for 153 levels of neutral cerium using time-resolved laser-induced fluorescence (TRLIF) on a slow beam of cerium atoms. Of the 153 levels studied, 150 are even parity and 3 are odd parity. The levels range in energy from 16 869 to 28 557 cm-1. This set of Ce I lifetimes is much more extensive than others published to date, and will provide the absolute calibration for a very large set of measured Ce I transition probabilities. Accurate transition probabilities for lines in the visible and ultraviolet are needed both in astrophysics, for the determination of elemental abundances, and by the lighting community, for research and development of metal halide high-intensity discharge lamps.

  2. Radiative lifetimes of neutral cerium

    Energy Technology Data Exchange (ETDEWEB)

    Den Hartog, E A; Buettner, K P; Lawler, J E [Department of Physics, University of Wisconsin, Madison, WI 53706 (United States)], E-mail: eadenhar@wisc.edu, E-mail: Kevin.Buettner@usma.edu, E-mail: jelawler@wisc.edu

    2009-04-28

    Radiative lifetimes, accurate to {+-}5%, have been measured for 153 levels of neutral cerium using time-resolved laser-induced fluorescence (TRLIF) on a slow beam of cerium atoms. Of the 153 levels studied, 150 are even parity and 3 are odd parity. The levels range in energy from 16 869 to 28 557 cm{sup -1}. This set of Ce I lifetimes is much more extensive than others published to date, and will provide the absolute calibration for a very large set of measured Ce I transition probabilities. Accurate transition probabilities for lines in the visible and ultraviolet are needed both in astrophysics, for the determination of elemental abundances, and by the lighting community, for research and development of metal halide high-intensity discharge lamps.

  3. Effects of microwave irradiation on metal hydrides and complex hydrides

    International Nuclear Information System (INIS)

    Effects of single-mode microwave irradiation on metal hydrides, MHn (LiH, MgH2, CaH2, TiH2, VH0.81, ZrH2, and LaH2.48) and complex hydrides MBH4 (LiBH4, NaBH4, and KBH4) were systematically investigated. Among the metal hydrides, TiH2, VH0.81, ZrH2, and LaH2.48 exhibit a rapid heating by microwave irradiation, where small amount of hydrogen (less than 0.5 mass%) are desorbed. On the other hand, LiBH4 is heated above 380 K by microwave irradiation, where 13.7 mass% of hydrogen is desorbed. The rapid heating of metal hydrides such as TiH2, VH0.81, ZrH2, and LaH2.48 are mainly due to the conductive loss. Meanwhile the microwave heating in LiBH4 is attributed to the conductive loss which is caused by a structural transition. The difference in the amount of desorbed hydrogen between metal hydrides and complex hydrides might be caused by the different microwave penetration depth and/or the temperature saturation in the microwave irradiation process. Microwave heating might be applied to hydrogen storage system, though further development of hydrides themselves and engineering techniques are required

  4. Preparation of metallic terbium and terbium hydride

    International Nuclear Information System (INIS)

    A method of metallic terbium preparation is described. The method consists in vacuum thermolysis of terbium hydride prepared as a result of terbium chloride interaction with lithium hydride. The prepared modification of terbium hydride demonstrates a high stability in the air. It is pointed out that problems arising from direct hydridation of the metal are responsible for certain advantages of the terbium hydride preparation method described

  5. Ab initio analysis of magnetovolume versus chemical effects in CeRuSi and its hydride

    Science.gov (United States)

    Matar, Samir F.

    2007-03-01

    The change from heavy fermion to antiferromagnetic behavior of intermetallic system CeRuSi upon hydrogenation is addressed on bases of lattice expansion and chemical bonding effects within the density-functional theoretical framework using all electron scalar-relativistic augmented spherical wave method. While no magnetic moment develops in the 111 system, from total-energy differences, the hydride is found to be stable as an antiferromagnet in the ground state, in agreement with experiment. The role of anisotropic lattice expansion induced by hydrogen insertion is shown to be prevailing over the chemical bonding between hydrogen and the metallic species especially cerium.

  6. Thermal coupling of a high temperature PEM fuel cell with a complex hydride tank

    DEFF Research Database (Denmark)

    Pfeifer, P.; Wall, C.; Jensen, Jens Oluf;

    2009-01-01

    Sodium alanate doped with cerium catalyst has been proven to have fast kinetics for hydrogen ab- and de-sorption as well as a high gravimetric storage density around 5 wt%. The kinetics of hydrogen sorption can be improved by preparing the alanate as nanocrystalline material. However, the second...... (including efficiency) as well as alanate kinetics were varied by system modelling with gPROMS (R). The kinetics of the hydride decomposition was found to have a major influence on the performance of the system. A cumulative output of 0.8 kWh was reached in a test run....

  7. Erbium hydride decomposition kinetics.

    Energy Technology Data Exchange (ETDEWEB)

    Ferrizz, Robert Matthew

    2006-11-01

    Thermal desorption spectroscopy (TDS) is used to study the decomposition kinetics of erbium hydride thin films. The TDS results presented in this report are analyzed quantitatively using Redhead's method to yield kinetic parameters (E{sub A} {approx} 54.2 kcal/mol), which are then utilized to predict hydrogen outgassing in vacuum for a variety of thermal treatments. Interestingly, it was found that the activation energy for desorption can vary by more than 7 kcal/mol (0.30 eV) for seemingly similar samples. In addition, small amounts of less-stable hydrogen were observed for all erbium dihydride films. A detailed explanation of several approaches for analyzing thermal desorption spectra to obtain kinetic information is included as an appendix.

  8. Metal hydride air conditioner

    Institute of Scientific and Technical Information of China (English)

    YANG; Ke; DU; Ping; LU; Man-qi

    2005-01-01

    The relationship among the hydrogen storage properties, cycling characteristics and thermal parameters of the metal hydride air conditioning systems was investigated. Based on a new alloy selection model, three pairs of hydrogen storage alloys, LaNi4.4 Mn0.26 Al0.34 / La0.6 Nd0.4 Ni4.8 Mn0.2 Cu0. 1, LaNi4.61Mn0. 26 Al0.13/La0.6 Nd0.4 Ni4.8 Mn0.2 Cu0. 1 and LaNi4.61 Mn0.26 Al0.13/La0.6 Y0.4 Ni4.8 Mn0. 2, were selected as the working materials for the metal hydride air conditioning system. Studies on the factors affecting the COP of the system showed that higher COP and available hydrogen content need the proper operating temperature and cycling time,large hydrogen storage capacity, flat plateau and small hysterisis of hydrogen alloys, proper original input hydrogen content and mass ratio of the pair of alloys. It also needs small conditioning system was established by using LaNi4.61 Mn0.26 Al0. 13/La0.6 Y0.4 Ni4.8 Mn0.2 alloys as the working materials, which showed that under the operating temperature of 180℃/40℃, a low temperature of 13℃ was reached, with COP =0.38 and Wnet =0.09 kW/kg.

  9. Hydride development for hydrogen storage

    Energy Technology Data Exchange (ETDEWEB)

    Thomas, G.J.; Guthrie, S.E.; Bauer, W.; Yang, N.Y.C. [Sandia National Lab., Livermore, CA (United States); Sandrock, G. [SunaTech, Inc., Ringwood, NJ (United States)

    1996-10-01

    The purpose of this project is to develop and demonstrate improved hydride materials for hydrogen storage. The work currently is organized into four tasks: hydride development, bed fabrication, materials support for engineering systems, and IEA Annex 12 activities. At the present time, hydride development is focused on Mg alloys. These materials generally have higher weight densities for storing hydrogen than rare earth or transition metal alloys, but suffer from high operating temperatures, slow kinetic behavior and material stability. The authors approach is to study bulk alloy additions which increase equilibrium overpressure, in combination with stable surface alloy modification and particle size control to improve kinetic properties. This work attempts to build on the considerable previous research in this area, but examines specific alloy systems in greater detail, with attention to known phase properties and structures. The authors have found that specific phases can be produced which have significantly improved hydride properties compared to previous studies.

  10. Complex Hydrides for Hydrogen Storage

    Energy Technology Data Exchange (ETDEWEB)

    Slattery, Darlene; Hampton, Michael

    2003-03-10

    This report describes research into the use of complex hydrides for hydrogen storage. The synthesis of a number of alanates, (AIH4) compounds, was investigated. Both wet chemical and mechano-chemical methods were studied.

  11. Low density metal hydride foams

    International Nuclear Information System (INIS)

    Disclosed is a low density foam having a porosity of from 0 to 98% and a density less than about 0.67 gm/cc, prepared by heating a mixture of powered lithium hydride and beryllium hydride in an inert atmosphere at a temperature ranging from about 455 to about 490 K for a period of time sufficient to cause foaming of said mixture, and cooling the foam thus produced. Also disclosed is the process of making the foam. 6 figures

  12. Geoneutrino and Hydridic Earth model

    CERN Document Server

    Bezrukov, Leonid

    2013-01-01

    Uranium, Thorium and Potassium-40 abundances in the Earth were calculated in the frame of Hydridic Earth model. Terrestrial heat producton from U, Th and K40 decays was calculated also. We must admit the existance of Earth expansion process to understand the obtained large value of terrestrial heat producton. The geoneutrino detector with volume more than 5 kT (LENA type) must be constructed to definitely separate between Bulk Silicat Earth model and Hydridic Earth model.

  13. Mechanical properties and fracture of titanium hydrides

    International Nuclear Information System (INIS)

    Titanium hydrides tend to suffer fracture when their thicknesses reach a critical thickness. Morphology and mechanical property of the hydrides are, however, not well known. The study aims to reveal the hydride morphology and fracture types of the hydrides. Chevron shaped plate hydrides were found to be produced on the surface of pure titanium (Grade 1) and Grade 7 titanium absorbing hydrogen. There were tree types of fracture of the hydrides, i.e., crack in hydride layer, exfoliation of the layer and shear-type fracture of the hydride plates, during the growth of the hydrides and deformation. We next estimated the true stress-strain curves of the hydrides on Grade 1 and 7 titanium using the dual Vickers indentation method, and the critical strain causing the Mode-I fine crack by indentation. Fracture strength and strain of the hydrides in Grade 1 titanium were estimated as 566 MPa and 4.5%, respectively. Those of the hydride in Grade 7 titanium were 498 MPa and 16%. Though the fracture strains estimated from the plastic instability of true stress-strain curves were approximately the half of those estimated by finite element method, the titanium hydrides were estimated to possess some extent of toughness or plastic deformation capability. (author)

  14. Inhibited oxidation of polymethylsiloxane, containing cerium

    International Nuclear Information System (INIS)

    The kinetics of oxidation of oligomeric polydimethylsiloxane in the presence of cerium-containing organosilicon antioxidant at 285-310 deg was investigated. High energy of activation for initiation process (around 272 kJ/mole) was established as a feature specific for chain oxidation of polydimethylsiloxane. It was found that cerium-containing antioxidant, as well as the iron-containing one, based on iron capronate, is of the ''depleting'' inhibitors, i.e. it looses its inhibiting ability during oxidation

  15. Electrodeposition of Oriented Cerium Oxide Films

    OpenAIRE

    Golden, Teresa D.; Adele Qi Wang

    2013-01-01

    Cerium oxide films of preferred orientation are electrodeposited under anodic conditions. A complexing ligand, acetate, was used to stabilize the cerium (III) ion in solution for deposition of the thin films. Fourier transform infrared spectroscopy showed that the ligand and metal tended to bind as a weakly bidentate complex. The crystallite size of the films was in the nanometer range as shown by Raman spectroscopy and was calculated from X-ray diffraction data. Crystallite sizes from 6 to 2...

  16. Ionic flotation of cerium, praseodymium and neodymium

    International Nuclear Information System (INIS)

    The possibility of practically complete flotation extraction of cerium, praseodymium and neodymium ions collected with the help of potassium abietate is shown. It is established that the most complete flotation extraction of cerium, praseodymium and neodymium ions takes place from solutions having 6-8 pH value in the presence of 1.5-2.5 multiple collector surplus. Solution temperature increase from 20 to 80 deg influences positively the flotation process

  17. Pharmacological potential of cerium oxidenanoparticles

    Science.gov (United States)

    Celardo, Ivana; Pedersen, Jens Z.; Traversa, Enrico; Ghibelli, Lina

    2011-04-01

    Nanotechnology promises a revolution in pharmacology to improve or create ex novo therapies. Cerium oxidenanoparticles (nanoceria), well-known as catalysts, possess an astonishing pharmacological potential due to their antioxidant properties, deriving from a fraction of Ce3+ ions present in CeO2. These defects, compensated by oxygen vacancies, are enriched at the surface and therefore in nanosized particles. Reactions involving redox cycles between the Ce3+ and Ce4+oxidation states allow nanoceria to react catalytically with superoxide and hydrogen peroxide, mimicking the behavior of two key antioxidant enzymes, superoxide dismutase and catalase, potentially abating all noxious intracellularreactive oxygen species (ROS) via a self-regenerating mechanism. Hence nanoceria, apparently well tolerated by the organism, might fight chronic inflammation and the pathologies associated with oxidative stress, which include cancer and neurodegeneration. Here we review the biological effects of nanoceria as they emerge from in vitro and in vivo studies, considering biocompatibility and the peculiar antioxidant mechanisms.

  18. Hydrogen storage in magnesium-based hydrides and hydride composites

    International Nuclear Information System (INIS)

    Mg and Mg-based hydrides have attracted much attention because of their high gravimetric hydrogen storage densities and favourable kinetic properties. Due to novel preparation methods and the development of suitable catalysts, hydrogen uptake and desorption is now possible within less than 2 min. However, the hydrogen reaction enthalpy of pure Mg is too high for many applications, for example, for the zero emission car. Therefore, different routes are explored to tailor the hydrogen reaction enthalpy to potential applications. This article summarizes the recent developments concerning sorption properties and thermodynamics of Mg-based hydrides for hydrogen storage applications. In particular, promising strategies to decrease the hydrogen reaction enthalpy by alloying and the use of reactive hydride composites are discussed

  19. A New Reducing Regent: Dichloroindium Hydride

    Institute of Scientific and Technical Information of China (English)

    A. BABA; I. SHIBATA; N. HAYASHI

    2005-01-01

    @@ 1Introduction Among the hydride derivatives of group 13 elements, various types of aluminum hydrides and boron hydrides have been employed as powerful reduction tools. Indium hydrides have not received much attention,whereas the synthesis of indium trihydride (InH3) was reported several decades ago[1]. There have been no precedents for monometallic indium hydrides having practical reactivity, while activated hydrides such as an ate complex LiPhn InH4-n (n = 0- 2) and phosphine-coordinated indium hydrides readily reduce carbonyl compounds. In view of this background, we focused on the development of dichloroindium hydrides (Cl2InH) as novel reducing agents that bear characteristic features in both ionic and radical reactions.

  20. Luminescent properties of aluminum hydride

    International Nuclear Information System (INIS)

    We studied cathodoluminescence and photoluminescence of α-AlH3– a likely candidate for use as possible hydrogen carrier in hydrogen-fueled vehicles. Luminescence properties of original α-AlH3 and α-AlH3 irradiated with ultraviolet were compared. The latter procedure leads to activation of thermal decomposition of α-AlH3 and thus has a practical implementation. We showed that the original and UV-modified aluminum hydride contain luminescence centers ‐ structural defects of the same type, presumably hydrogen vacancies, characterized by a single set of characteristic bands of radiation. The observed luminescence is the result of radiative intracenter relaxation of the luminescence center (hydrogen vacancy) excited by electrons or photons, and its intensity is defined by the concentration of vacancies, and the area of their possible excitation. UV-activation of the dehydrogenation process of aluminum hydride leads to changes in the spatial distribution of the luminescence centers. For short times of exposure their concentration increases mainly in the surface regions of the crystals. At high exposures, this process extends to the bulk of the aluminum hydride and ends with a decrease in concentration of luminescence centers in the surface region. - Highlights: • Aluminum hydride contains hydrogen vacancies which serve as luminescence centers. • The luminescence is the result of radiative relaxation of excited centers. • Hydride UV-irradiation alters distribution and concentration of luminescence centers

  1. Luminescent properties of aluminum hydride

    Energy Technology Data Exchange (ETDEWEB)

    Baraban, A.P.; Gabis, I.E.; Dmitriev, V.A. [Saint-Petersburg State University, Department of Physics, Saint-Petersburg 198504 (Russian Federation); Dobrotvorskii, M.A., E-mail: mstislavd@gmail.com [Saint-Petersburg State University, Department of Physics, Saint-Petersburg 198504 (Russian Federation); Kuznetsov, V.G. [Saint-Petersburg State University, Department of Physics, Saint-Petersburg 198504 (Russian Federation); Matveeva, O.P. [National Mineral Resources University, Saint Petersburg 199106 (Russian Federation); Titov, S.A. [Petersburg State University of Railway Transport, Saint-Petersburg 190031 (Russian Federation); Voyt, A.P.; Elets, D.I. [Saint-Petersburg State University, Department of Physics, Saint-Petersburg 198504 (Russian Federation)

    2015-10-15

    We studied cathodoluminescence and photoluminescence of α-AlH{sub 3}– a likely candidate for use as possible hydrogen carrier in hydrogen-fueled vehicles. Luminescence properties of original α-AlH{sub 3} and α-AlH{sub 3} irradiated with ultraviolet were compared. The latter procedure leads to activation of thermal decomposition of α-AlH{sub 3} and thus has a practical implementation. We showed that the original and UV-modified aluminum hydride contain luminescence centers ‐ structural defects of the same type, presumably hydrogen vacancies, characterized by a single set of characteristic bands of radiation. The observed luminescence is the result of radiative intracenter relaxation of the luminescence center (hydrogen vacancy) excited by electrons or photons, and its intensity is defined by the concentration of vacancies, and the area of their possible excitation. UV-activation of the dehydrogenation process of aluminum hydride leads to changes in the spatial distribution of the luminescence centers. For short times of exposure their concentration increases mainly in the surface regions of the crystals. At high exposures, this process extends to the bulk of the aluminum hydride and ends with a decrease in concentration of luminescence centers in the surface region. - Highlights: • Aluminum hydride contains hydrogen vacancies which serve as luminescence centers. • The luminescence is the result of radiative relaxation of excited centers. • Hydride UV-irradiation alters distribution and concentration of luminescence centers.

  2. Hydrogen, lithium, and lithium hydride production

    Science.gov (United States)

    Brown, Sam W; Spencer, Larry S; Phillips, Michael R; Powell, G. Louis; Campbell, Peggy J

    2014-03-25

    A method of producing high purity lithium metal is provided, where gaseous-phase lithium metal is extracted from lithium hydride and condensed to form solid high purity lithium metal. The high purity lithium metal may be hydrided to provide high purity lithium hydride.

  3. Thermomechanical properties of hafnium hydride

    International Nuclear Information System (INIS)

    Fine bulk samples of delta-phase Hf hydride with various hydrogen contents (CH) ranging from 1.62 to 1.72 in the atomic ratio (H/Hf) were prepared, and their thermomechanical properties were characterized. At room temperature, the sound velocity and Vickers hardness were measured. The elastic modulus was calculated from the measured sound velocity. In the temperature range from room temperature to 673 K, the thermal expansion was measured by using a dilatometer, and the linear thermal expansion coefficient was calculated. Empirical equations describing the thermomechanical properties of Hf hydride as a function of CH were proposed. (author)

  4. Properties of nanoscale metal hydrides

    International Nuclear Information System (INIS)

    Nanoscale hydride particles may exhibit chemical stabilities which differ from those of a macroscopic system. The stabilities are mainly influenced by a surface energy term which contains size-dependent values of the surface tension, the molar volume and an additional term which takes into account a potential reduction of the excess surface energy. Thus, the equilibrium of a nanoparticular hydride system may be shifted to the hydrogenated or to the dehydrogenated side, depending on the size and on the prefix of the surface energy term of the hydrogenated and dehydrogenated material. Additional complexity appears when solid-state reactions of complex hydrides are considered and phase segregation has to be taken into account. In such a case the reversibility of complex hydrides may be reduced if the nanoparticles are free standing on a surface. However, it may be enhanced if the system is enclosed by a nanoscale void which prevents the reaction partners on the dehydrogenated side from diffusing away from each other. Moreover, the generally enhanced diffusivity in nanocrystalline systems may lower the kinetic barriers for the material's transformation and, thus, facilitate hydrogen absorption and desorption.

  5. Optimization of process efficiency in cerium electrorefining

    International Nuclear Information System (INIS)

    Reactive metal electrorefining presents a number of problems that pose daunting obstacles to commercial operation. Typical reduction of reactive metal oxides or halide can introduce a variety of impurities such as iron, nickel, chromium, silicon, aluminum and various other metals which must be removed. This research program has addressed the various parameters of molten salt electrorefining of cerium metal to provide insight to this extremely important process. Cerium has been chosen as the surrogate for certain reactive metals on account of its similar electrochemical characteristics. The justification for such a choice has been investigated. The cell components and configuration, current efficiency of the process, purity of the cathodically deposited metal and the power requirement of the system have been optimized in a molten calcium chloride salt electrolyte using a molten, stirred impure metal anode. Various refractory crucible design and electrode materials have been studied to improve the process reliability. The equimolar NaKCl2 salt used in the electrorefining of some reactive metals is found to be inappropriate as a relatively high temperature is required to electrorefine cerium, i.e. melting point of Ce [798 C]. The homogeneity of the anode is controlled by the stirring at an optimized rate. This paper highlights the validity of cerium oxide and intermetallics of cerium as a surrogate for other reactive metal oxides or the respective intermetallics

  6. Deformation of vanadium and niobium on hydridation

    International Nuclear Information System (INIS)

    Deformation of wire samples made of polycrystalline vanadium and niobium on hydridation is studied. It is shown that sample allowance under loading after deformation below the yield strength doesn't cause considerable creep. Cathode saturation of samples with hydrogen sharply accelerates vanadium microdeformation velocity, that is connected with the beginning of intensive vanadium hydride precipitation (β-phase) from α-solid vanadium-hydrogen solution. Niobium hydridation at the first stage doesn't hydridation at the first stage doesn't cause negative deformation, then change in deformation direction takes place at the moment of intensive growth of the hydride phase. The conclusion is made that in both metals microdeformation is determined by contribution of two components: deformation caused by changing a shift module of metal-hydrogen system, and deformation caused by the oriented growth of the hydride phase in the field of apphed stresses

  7. Anodematerials for Metal Hydride Batteries

    DEFF Research Database (Denmark)

    Jensen, Jens Oluf

    1997-01-01

    This report describes the work on development of hydride forming alloys for use as electrode materials in metal hydride batteries. The work has primarily been concentrated on calcium based alloys derived from the compound CaNi5. This compound has a higher capacity compared with alloys used in today...... was developed. The parameters milling time, milling intensity, number of balls and form of the alloying metals were investigated. Based on this a final alloying technique for the subsequent preparation of electrode materials was established. The technique comprises milling for 4 hours twice possibly...... followed by annealing at 700°C for 12 hours. The alloys appeared to be nanocrystalline with an average crystallite size around 10 nm before annealing. Special steel containers was developed for the annealing of the metal powders in inert atmosphere. The use of various annealing temperatures was...

  8. Tritium processing using metal hydrides

    International Nuclear Information System (INIS)

    E.I. duPont de Nemours and Company is commissioned by the US Department of Energy to operate the Savannah River Plant and Laboratory. The primary purpose of the plant is to produce radioactive materials for national defense. In keeping with current technology, new processes for the production of tritium are being developed. Three main objectives of this new technology are to ease the processing of, ease the storage of, and to reduce the operating costs of the tritium production facility. Research has indicated that the use of metal hydrides offers a viable solution towards satisfying these objectives. The Hydrogen and Fuels Technology Division has the responsibility to conduct research in support of the tritium production process. Metal hydride technology and its use in the storage and transportation of hydrogen will be reviewed

  9. Study of the discharge ionization of cerium at a solid-paste graphite electrode

    International Nuclear Information System (INIS)

    The discharge ionization of cerium(3) at a solid-paste graphite electrode was studied by stripping voltametry. The optimal conditions for the concentration and following determination of cerium in 1 x 10-4 - 1 x 10-6 M cerium(3) solutions were found. The conditional constant of cerium(4) reduction to cerium(3) was also calculated

  10. Drying dichloromethane over calcium hydride

    OpenAIRE

    sprotocols

    2015-01-01

    Authors: Lucas Kinard, Kurtis Kasper & Antonios Mikos ### Abstract This protocol describes the drying of dichloromethane by a simple 10 step procedure. One can implement this protocol using common lab glass and lab equipment. First, dichloromethane is refluxed with calcium hydride to remove water. Then, dichloromethane is distilled to separate it from the byproducts of the reflux reaction. This procedure can be implemented in 1 day. ### Introduction In many instances i...

  11. Complex hydrides for hydrogen storage

    Science.gov (United States)

    Zidan, Ragaiy

    2006-08-22

    A hydrogen storage material and process of forming the material is provided in which complex hydrides are combined under conditions of elevated temperatures and/or elevated temperature and pressure with a titanium metal such as titanium butoxide. The resulting fused product exhibits hydrogen desorption kinetics having a first hydrogen release point which occurs at normal atmospheres and at a temperature between 50.degree. C. and 90.degree. C.

  12. Nanostructured, complex hydride systems for hydrogen generation

    Directory of Open Access Journals (Sweden)

    Robert A. Varin

    2015-02-01

    Full Text Available Complex hydride systems for hydrogen (H2 generation for supplying fuel cells are being reviewed. In the first group, the hydride systems that are capable of generating H2 through a mechanical dehydrogenation phenomenon at the ambient temperature are discussed. There are few quite diverse systems in this group such as lithium alanate (LiAlH4 with the following additives: nanoiron (n-Fe, lithium amide (LiNH2 (a hydride/hydride system and manganese chloride MnCl2 (a hydride/halide system. Another hydride/hydride system consists of lithium amide (LiNH2 and magnesium hydride (MgH2, and finally, there is a LiBH4-FeCl2 (hydride/halide system. These hydride systems are capable of releasing from ~4 to 7 wt.% H2 at the ambient temperature during a reasonably short duration of ball milling. The second group encompasses systems that generate H2 at slightly elevated temperature (up to 100 °C. In this group lithium alanate (LiAlH4 ball milled with the nano-Fe and nano-TiN/TiC/ZrC additives is a prominent system that can relatively quickly generate up to 7 wt.% H2 at 100 °C. The other hydride is manganese borohydride (Mn(BH42 obtained by mechano-chemical activation synthesis (MCAS. In a ball milled (2LiBH4 + MnCl2 nanocomposite, Mn(BH42 co-existing with LiCl can desorb ~4.5 wt.% H2 at 100 °C within a reasonable duration of dehydrogenation. Practical application aspects of hydride systems for H2 generation/storage are also briefly discussed.

  13. Crystal structure of gold hydride

    International Nuclear Information System (INIS)

    Highlights: • Volume expansion of metal hydrides is due to the increase in the s-band filling. • AuH structure is similar to that of Hg having one more s electron compared to Au. • Structure stability of both Hg and AuH is governed by the Hume-Rothery rule. - Abstract: A number of transition metal hydrides with close-packed metal sublattices of fcc or hcp structures with hydrogen in octahedral interstitial positions were obtained by the high-pressure-hydrogen technique described by Ponyatovskii et al. (1982). In this paper we consider volume increase of metals by hydrogenation and possible crystal structure of gold hydride in relation with the structure of mercury, the nearest neighbor of Au in the Periodic table. Suggested structure of AuH has a basic tetragonal body-centered cell that is very similar to the mercury structure Hg-t I 2. The reasons of stability for this structure are discussed within the model of Fermi sphere–Brillouin zone interactions

  14. NMR study of hydride systems

    International Nuclear Information System (INIS)

    The hydrides of thorium (ThH2, Th4H15 and Th4D15) and the intermetallic compound system (Zr(Vsub(1-x)Cosub(x))2 and its hydrides were investigated using the nuclear magnetic resonance (NMR) technique. From the results for the thorium hydride samples it was concluded that the density of states at the Fermi level n(Esub(f)) is higher in Th4H15 than in ThH2; there is an indirect reaction between the protons and the d electrons belonging to the Th atoms in Th4H15; n(E) has a sharp structure near Esub(f). It was also found that the hydrogen diffusion mechanism changes with temperature. From the results for the intermetallic compound system conclusions were drawn concerning variations in the electronic structure, which explain the behavior of the system. In hydrogen diffusion studies in several samples it was found that Co atoms slow the diffusion rate. Quadrupole spectra obtained at low temperatures show that the H atoms preferably occupy tetrahedral sites formed by three V atoms and one Z atom. (H.K.)

  15. Crystal structure of gold hydride

    Energy Technology Data Exchange (ETDEWEB)

    Degtyareva, Valentina F., E-mail: degtyar@issp.ac.ru

    2015-10-05

    Highlights: • Volume expansion of metal hydrides is due to the increase in the s-band filling. • AuH structure is similar to that of Hg having one more s electron compared to Au. • Structure stability of both Hg and AuH is governed by the Hume-Rothery rule. - Abstract: A number of transition metal hydrides with close-packed metal sublattices of fcc or hcp structures with hydrogen in octahedral interstitial positions were obtained by the high-pressure-hydrogen technique described by Ponyatovskii et al. (1982). In this paper we consider volume increase of metals by hydrogenation and possible crystal structure of gold hydride in relation with the structure of mercury, the nearest neighbor of Au in the Periodic table. Suggested structure of AuH has a basic tetragonal body-centered cell that is very similar to the mercury structure Hg-t I 2. The reasons of stability for this structure are discussed within the model of Fermi sphere–Brillouin zone interactions.

  16. New layered functionalized cerium(IV) phenylphosphonates

    Czech Academy of Sciences Publication Activity Database

    Melánová, Klára; Beneš, L.; Svoboda, Jan; Zima, Vítězslav; Vlček, Milan

    Lille: European Materials Research Society, 2014. Q.PI-20. [E- MRS 2014 Spring Meeting. 26.05.2014-30.05.2014, Lille] R&D Projects: GA ČR(CZ) GA14-13368S Institutional support: RVO:61389013 Keywords : cerium * layered phosphonates * thermogravimetry Subject RIV: CA - Inorganic Chemistry

  17. Uptake and accumulation of bulk and nanosized cerium oxide particles and ionic cerium by radish (Raphanus sativus L.).

    Science.gov (United States)

    Zhang, Weilan; Ebbs, Stephen D; Musante, Craig; White, Jason C; Gao, Cunmei; Ma, Xingmao

    2015-01-21

    The potential toxicity and accumulation of engineered nanomaterials (ENMs) in agricultural crops has become an area of great concern and intense investigation. Interestingly, although below-ground vegetables are most likely to accumulate the highest concentrations of ENMs, little work has been done investigating the potential uptake and accumulation of ENMs for this plant group. The overall objective of this study was to evaluate how different forms of cerium (bulk cerium oxide, cerium oxide nanoparticles, and the cerium ion) affected the growth of radish (Raphanus sativus L.) and accumulation of cerium in radish tissues. Ionic cerium (Ce(3+)) had a negative effect on radish growth at 10 mg CeCl3/L, whereas bulk cerium oxide (CeO2) enhanced plant biomass at the same concentration. Treatment with 10 mg/L cerium oxide nanoparticles (CeO2 NPs) had no significant effect on radish growth. Exposure to all forms of cerium resulted in the accumulation of this element in radish tissues, including the edible storage root. However, the accumulation patterns and their effect on plant growth and physiological processes varied with the characteristics of cerium. This study provides a critical frame of reference on the effects of CeO2 NPs versus their bulk and ionic counterparts on radish growth. PMID:25531028

  18. Delayed hydride cracking in Zr-2.5 % Nb: effect of hydride blisters

    International Nuclear Information System (INIS)

    In the zirconium base alloys subjected to a local thermal gradient, in presence of hydrogen, fully hydride region (frequently called blisters) can be formed. Due to the brittle character of the zirconium hydride, cracks are usually found inside the blisters. These cracks are prone to growing, under stress and temperature, by successive hydride precipitation at the crack tip. This process is called hydride induced delayed cracking (HIDC). In a previous work, hydride platelets were observed in the radial direction of the blister. In the present one, blisters were grown on Zr-2.5 wt % Nb pressure tubes. Then, tensile specimens were submitted to HIDC tests. During the test, the radial hydrides length increase due to stress concentrator effect of the blister. If a crack, that was initiated into the blister, reaches the Zr matrix therefore can propagate through the radial hydrides. (author)

  19. Kinetics of hydride front in Zircaloy-2 and H release from a fractional hydrided surface

    Energy Technology Data Exchange (ETDEWEB)

    Diaz, M.; Gonzalez-Gonzalez, A.; Moya, J. S.; Remartinez, B.; Perez, S.; Sacedon, J. L. [Instituto de Ciencia de Materiales de Madrid (CSIC), Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain); Iberdrola, Tomas Redondo 3, 28033 Madrid (Spain); Instituto de Ciencia de Materiales de Madrid (CSIC), Sor Juana Ines de la Cruz 3, Cantoblanco, 28049 Madrid (Spain)

    2009-07-15

    The authors study the hydriding process on commercial nuclear fuel claddings from their inner surface using an ultrahigh vacuum method. The method allows determining the incubation and failure times of the fuel claddings, as well as the dissipated energy and the partial pressure of the desorbed H{sub 2} from the outer surface of fuel claddings during the hydriding process. The correlation between the hydriding dissipated energy and the amount of zirconium hydride (formed at different stages of the hydriding process) leads to a near t{sup 1/2} potential law corresponding to the time scaling of the reaction for the majority of the tested samples. The calibrated relation between energy and hydride thickness allows one to calculate the enthalpy of the {delta}-ZrH{sub 1.5} phase. The measured H{sub 2} desorption from the external surface is in agreement with a proposed kinetic desorption model from the hydrides precipitated at the surface.

  20. Predicting formation enthalpies of metal hydrides

    DEFF Research Database (Denmark)

    Andreasen, A.

    2004-01-01

    In order for the hydrogen based society viz. a society in which hydrogen is the primary energy carrier to become realizable an efficient way of storing hydrogen is required. For this purpose metal hydrides are serious candidates. Metal hydrides are formedby chemical reaction between hydrogen and ...

  1. Submillimeter Spectroscopy of Hydride Molecules

    Science.gov (United States)

    Phillips, T. G.

    1998-05-01

    Simple hydride molecules are of great importance in astrophysics and astrochemistry. Physically they dominate the cooling of dense, warm phases of the ISM, such as the cores and disks of YSOs. Chemically they are often stable end points of chemical reactions, or may represent important intermediate stages of the reaction chains, which can be used to test the validity of the process. Through the efforts of astronomers, physicists, chemists, and laboratory spectroscopists we have an approximate knowledge of the abundance of some of the important species, but a great deal of new effort will be required to achieve the comprehensive and accurate data set needed to determine the energy balance and firmly establish the chemical pathways. Due to the low moment of inertia, the hydrides rotate rapidly and so have their fundamental spectral lines in the submillimeter. Depending on the cloud geometry and temperature profile they may be observed in emission or absorption. Species such as HCl, HF, OH, CH, CH(+) , NH_2, NH_3, H_2O, H_2S, H_3O(+) and even H_3(+) have been detected, but this is just a fraction of the available set. Also, most deduced abundances are not nearly sufficiently well known to draw definitive conclusions about the chemical processes. For example, the most important coolant for many regions, H_2O, has a possible range of deduced abundance of a factor of 1000. The very low submillimeter opacity at the South Pole site will be a significant factor in providing a new capabilty for interstellar hydride spectroscopy. The new species and lines made available in this way will be discussed.

  2. Thermodynamic studies in the system cerium-gadolinium-oxygen

    International Nuclear Information System (INIS)

    Two independent measuring methods have been applied to studying the phase relations of the system cerium-gadolinium. The calorimetric measurements have been done in a high-temperature calorimeter with cerium dioxide doped with 10 mole % of Gd2O3. Further thermodynamic quantities have been obtained by the electrochemical method and e.m.f. measurements, yielding additional information on disorders in doped cerium dioxide. (orig./BBR)

  3. Electrochemical reduction of cerium oxide into metal

    International Nuclear Information System (INIS)

    The Fray Farthing and Chen (FFC) and Ono and Suzuki (OS) processes were developed for the reduction of titanium oxide to titanium metal by electrolysis in high temperature molten alkali chloride salts. The possible transposition to CeO2 reduction is considered in this study. Present work clarifies, by electro-analytical techniques, the reduction pathway leading to the metal. The reduction of CeO2 into metal was feasible via an indirect mechanism. Electrolyses on 10 g of CeO2 were carried out to evaluate the electrochemical process efficiency. Ca metal is electrodeposited at the cathode from CaCl2-KCl solvent and reacts chemically with ceria to form not only metallic cerium, but also cerium oxychloride.

  4. Electrochemical reduction of cerium oxide into metal

    Energy Technology Data Exchange (ETDEWEB)

    Claux, Benoit [CEA, Valduc, F-21120 Is-sur-Tille (France); Universite de Grenoble, LEPMI-ENSEEG, 1130 rue de la Piscine, BP75, F-38402 St Martin d' Heres Cedex (France); Serp, Jerome, E-mail: jerome.serp@cea.f [CEA, Valduc, F-21120 Is-sur-Tille (France); Fouletier, Jacques [Universite de Grenoble, LEPMI-ENSEEG, 1130 rue de la Piscine, BP75, F-38402 St Martin d' Heres Cedex (France)

    2011-02-28

    The Fray Farthing and Chen (FFC) and Ono and Suzuki (OS) processes were developed for the reduction of titanium oxide to titanium metal by electrolysis in high temperature molten alkali chloride salts. The possible transposition to CeO{sub 2} reduction is considered in this study. Present work clarifies, by electro-analytical techniques, the reduction pathway leading to the metal. The reduction of CeO{sub 2} into metal was feasible via an indirect mechanism. Electrolyses on 10 g of CeO{sub 2} were carried out to evaluate the electrochemical process efficiency. Ca metal is electrodeposited at the cathode from CaCl{sub 2}-KCl solvent and reacts chemically with ceria to form not only metallic cerium, but also cerium oxychloride.

  5. Cerium and jojoba in engines?; Cerium et jojoba dans les moteurs?

    Energy Technology Data Exchange (ETDEWEB)

    Massy-Delhotel, E.

    1996-10-01

    The Belgium company CreaTel proposes a new system, called Forac, which can lead to a 10% reduction of fuel consumption in thermal engines together with a quasi-complete reduction of CO, HC, NOx pollutants and CO{sub 2} particulates emission. The system comprises a steam production device and an admission pipe with a cerium alloy whorl inside. The steam produced is mixed with the admission air and tears cerium particles from the inside of the admission pipe to the combustion chamber. The cerium particles act as a catalyst which favours the complete combustion of the fuel. The same company proposes also lubricant additives made from liquid jojoba wax which allow the reduction of pollutant emissions, fuel consumption and noise emissions of diesel engines. (J.S.)

  6. Activated aluminum hydride hydrogen storage compositions and uses thereof

    Science.gov (United States)

    Sandrock, Gary; Reilly, James; Graetz, Jason; Wegrzyn, James E.

    2010-11-23

    In one aspect, the invention relates to activated aluminum hydride hydrogen storage compositions containing aluminum hydride in the presence of, or absence of, hydrogen desorption stimulants. The invention particularly relates to such compositions having one or more hydrogen desorption stimulants selected from metal hydrides and metal aluminum hydrides. In another aspect, the invention relates to methods for generating hydrogen from such hydrogen storage compositions.

  7. Hydrogen-storing hydride complexes

    Science.gov (United States)

    Srinivasan, Sesha S.; Niemann, Michael U.; Goswami, D. Yogi; Stefanakos, Elias K.

    2012-04-10

    A ternary hydrogen storage system having a constant stoichiometric molar ratio of LiNH.sub.2:MgH.sub.2:LiBH.sub.4 of 2:1:1. It was found that the incorporation of MgH.sub.2 particles of approximately 10 nm to 20 nm exhibit a lower initial hydrogen release temperature of 150.degree. C. Furthermore, it is observed that the particle size of LiBNH quaternary hydride has a significant effect on the hydrogen sorption concentration with an optimum size of 28 nm. The as-synthesized hydrides exhibit two main hydrogen release temperatures, one around 160.degree. C. and the other around 300.degree. C., with the main hydrogen release temperature reduced from 310.degree. C. to 270.degree. C., while hydrogen is first reversibly released at temperatures as low as 150.degree. C. with a total hydrogen capacity of 6 wt. % to 8 wt. %. Detailed thermal, capacity, structural and microstructural properties have been demonstrated and correlated with the activation energies of these materials.

  8. Experimental reproducibility analysis in DU hydriding

    Energy Technology Data Exchange (ETDEWEB)

    Koo, Daeseo; Park, Jongcheol; Chung, Hongsuk [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2014-10-15

    A storage and delivery system (SDS) is used for storing hydrogen isotopes as a metal hydride form. The rapid hydriding of tritium is very important not only for safety reasons but also for the economic design and operation of the SDS. For the storage, supply, and recovery of hydrogen isotopes, depleted uranium (DU) has been extensively proposed. To develop nuclear fusion technology, it will be necessary to store and supply hydrogen isotopes needed for Tokamak operation. The experimental reproducibility of bed temperature on DU hydriding was also analyzed. The experimental reproducibility of apparatus was acceptable for all the experiments. The experimental reproducibility of tank pressure on DU hydriding was analyzed. As the hydriding performs, the tank pressure showed decreasing trend. The experimental reproducibility of bed temperature on DU hydriding was also analyzed. As the hydriding performs, the bed temperatures increased up to maximum temperature with exothermic reaction and then they showed decreasing trend. The experimental reproducibility of apparatus was acceptable for all the experiments.

  9. Hydriding failure analysis based on PIE data

    International Nuclear Information System (INIS)

    Failure causes of the two fuel rods of a Korean nuclear power plant had been investigated by using PIE technique. The destructive and physico-chemical examinations revealed that the clad hydriding phenomena had caused the rod failures primarily and secondarily in each case. In this study the basic mechanisms of the primary and the secondary hydriding failures are reviewed, PIE data such as cladding inner and outer surface oxide thickness and the restructuring of fuel pellets are analyzed, and they are compared with predicted behaviors by a fuel performance code. The results strongly support that the hydriding processes, primary and secondary, had played critical roles in the respective fuel rods failures. (author)

  10. Solid hydrides as hydrogen storage reservoirs

    International Nuclear Information System (INIS)

    Metal hydrides as hydrogen storage materials are briefly reviewed in this paper. Fundamental properties of metal-hydrogen (gas) system such as Pressure-Composition-Temperature (P-C-T) characteristics are discussed on the light of the metal-hydride thermodynamics. Attention is specially paid to light metal hydrides which might have application in the car and transport sector. The pros and cons of MgH2 as a light material are outlined. Researches in course oriented to improve the behaviour of MgH2 are presented. Finally, other very promising alternative materials such as Al compounds (alanates) or borohydrides as light hydrogen accumulators are also considered. (Author)

  11. Hydride observations using the neutrography technique

    International Nuclear Information System (INIS)

    Neutron radiography observations were performed at the RA-6 experimental nuclear facility in Bariloche. Images from a prototype of a hydride-based hydrogen storage device have been obtained. The technique allows visualizing the inner hydride space distribution. The hydride appeared compacted at the lower part of the prototype after several cycles of hydrogen charge and discharge. The technique has also been applied to the study of Zr/ZrH2 samples. There is a linear relation between the sample width/hydrogen concentration and the photograph grey scale. This information could be useful for the study of nuclear engineering materials and to determine their possible degradation by hydrogen pick up (author)

  12. The electrochemical impedance of metal hydride electrodes

    DEFF Research Database (Denmark)

    Valøen, Lars Ole; Lasia, Andrzej; Jensen, Jens Oluf; Tunold, Reidar

    2002-01-01

    The electrochemical impedance responses for different laboratory type metal hydride electrodes were successfully modeled and fitted to experimental data for AB5 type hydrogen storage alloys as well as one MgNi type electrode. The models fitted the experimental data remarkably well. Several AC......, explaining the experimental impedances in a wide frequency range for electrodes of hydride forming materials mixed with copper powder, were obtained. Both charge transfer and spherical diffusion of hydrogen in the particles are important sub processes that govern the total rate of the electrochemical...... observed. The impedance analysis was found to be an efficient method for characterizing metal hydride electrodes in situ....

  13. DFT modeling of the electronic and magnetic structures and chemical bonding properties of intermetallic hydrides

    International Nuclear Information System (INIS)

    This thesis presents an ab initio study of several classes of intermetallics and their hydrides. These compounds are interesting from both a fundamental and an applied points of view. To achieve this aim two complementary methods, constructed within the DFT, were chosen: (i) pseudo potential based VASP for geometry optimization, structural investigations and electron localization mapping (ELF), and (ii) all-electrons ASW method for a detailed description of the electronic structure, chemical bonding properties following different schemes as well as quantities depending on core electrons such as the hyperfine field. A special interest is given with respect to the interplay between magneto-volume and chemical interactions (metal-H) effects within the following hydrided systems: binary Laves (e.g. ScFe2) and Haucke (e.g. LaNi5) phases on one hand, and ternary cerium based (e.g. CeRhSn) and uranium based (e.g. U2Ni2Sn) alloys on the other hand. (author)

  14. Structural, optical, morphological and dielectric properties of cerium oxide nanoparticles

    International Nuclear Information System (INIS)

    Cerium oxide (CeO2) nanoparticles were prepared by the precipitation method. The average crystallite size of cerium oxide nanoparticles was calculated from the X-ray diffraction (XRD) pattern and found to be 11 nm. The FT-IR spectrum clearly indicated the strong presence of cerium oxide nanoparticles. Raman spectrum confirmed the cubic nature of the cerium oxide nanoparticles. The Scanning Electron Microscopy (SEM) analysis showed that the nanoparticles agglomerated forming spherical-shaped particles. The Transmission Electron Microscopic (TEM) analysis confirmed the prepared cerium oxide nanoparticles with the particle size being found to be 16 nm. The optical absorption spectrum showed a blue shift by the cerium oxide nanoparticles due to the quantum confinement effect. The dielectric properties of cerium oxide nanoparticles were studied for different frequencies at different temperatures. The dielectric constant and the dielectric loss of the cerium oxide nanoparticles decreased with increase in frequency. The AC electrical conductivity study revealed that the conduction depended on both the frequency and the temperature. (author)

  15. Structural, optical, morphological and dielectric properties of cerium oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Prabaharan, Devadoss Mangalam Durai Manoharadoss [Department of Physics, NPR College of Engineering and Technology, Natham, Dindigul, Tamil Nadu (India); Sadaiyandi, Karuppasamy [Department of Physics, Alagappa Government Arts College, Karaikudi, Sivaganga, Tamil Nadu (India); Mahendran, Manickam [Department of Physics, Thiagarajar College of Engineering, Madurai, Tamil Nadu (India); Sagadevan, Suresh, E-mail: duraiphysics2011@gmail.com [Department of Physics, AMET University (India)

    2016-03-15

    Cerium oxide (CeO{sub 2}) nanoparticles were prepared by the precipitation method. The average crystallite size of cerium oxide nanoparticles was calculated from the X-ray diffraction (XRD) pattern and found to be 11 nm. The FT-IR spectrum clearly indicated the strong presence of cerium oxide nanoparticles. Raman spectrum confirmed the cubic nature of the cerium oxide nanoparticles. The Scanning Electron Microscopy (SEM) analysis showed that the nanoparticles agglomerated forming spherical-shaped particles. The Transmission Electron Microscopic (TEM) analysis confirmed the prepared cerium oxide nanoparticles with the particle size being found to be 16 nm. The optical absorption spectrum showed a blue shift by the cerium oxide nanoparticles due to the quantum confinement effect. The dielectric properties of cerium oxide nanoparticles were studied for different frequencies at different temperatures. The dielectric constant and the dielectric loss of the cerium oxide nanoparticles decreased with increase in frequency. The AC electrical conductivity study revealed that the conduction depended on both the frequency and the temperature. (author)

  16. Tritium removal using vanadium hydride

    International Nuclear Information System (INIS)

    The results of an initial examination of the feasibility of separation of tritium from gaseous protium-tritium mixtures using vanadium hydride in cyclic processes is reported. Interest was drawn to the vanadium-hydrogen system because of the so-called inverse isotope effect exhibited by this system. Thus the tritide is more stable than the protide, a fact which makes the system attractive for removal of tritium from a mixture in which the light isotope predominates. The initial results of three phases of the research program are reported, dealing with studies of the equilibrium and kinetics properties of isotope exchange, development of an equilibrium theory of isotope separation via heatless adsorption, and experiments on the performance of a single heatless adsorption stage. In the equilibrium and kinetics studies, measurements were made of pressure-composition isotherms, the HT--H2 separation factors and rates of HT--H2 exchange. This information was used to evaluate constants in the theory and to understand the performance of the heatless adsorption experiments. A recently developed equilibrium theory of heatless adsorption was applied to the HT--H2 separation using vanadium hydride. Using the theory it was predicted that no separation would occur by pressure cycling wholly within the β phase but that separation would occur by cycling between the β and γ phases and using high purge-to-feed ratios. Heatless adsorption experiments conducted within the β phase led to inverse separations rather than no separation. A kinetic isotope effect may be responsible. Cycling between the β and γ phases led to separation but not to the predicted complete removal of HT from the product stream, possibly because of finite rates of exchange. Further experimental and theoretical work is suggested which may ultimately make possible assessment of the feasibility and practicability of hydrogen isotope separation by this approach

  17. Radiation induced color centers in cerium-doped and cerium-free multicomponent silicate glasses

    Institute of Scientific and Technical Information of China (English)

    傅鑫杰; 宋力昕; 李家成

    2014-01-01

    The effect of doped cerium on the radiation-resistance behavior of silicate glass was investigated in our work. The ultra-violet-visible absorption spectra and electron paramagnetic resonance (EPR) spectra were obtained after the cerium-rich and ce-rium-free multicomponent silicate glasses (K509 and K9) were irradiated by gamma rays with a dose range from 10 to 1000 kGy. The results showed that E’ center, oxygen deficient center (ODC) and non-bridging oxygen hole center (HC1 and HC2) were induced in K9 and K509 glasses after radiation. The concentrations of all color centers presented an exponential growth with the increase of the gamma dose. Moreover, the concentration of HC1 and HC2 in cerium-doped K509 glass was much lower than that in cerium-free K9 glass at the same dose of radiation, which could be attributed to the following mechanism:Ce3+ions capturing holes then forming Ce3++centers inhibited the formation of hole trapped color centers (HC1 and HC2) and Ce4+ions capturing electrons to form Ce3+centers suppressed the formation of electron trapped color centers like E’ center.

  18. Geoneutrino and Hydridic Earth model. Version 2

    OpenAIRE

    Bezrukov, Leonid

    2013-01-01

    Uranium, Thorium and Potassium-40 abundances in the Earth were calculated in the frame of Hydridic Earth model. Terrestrial heat producton from U, Th and K40 decays was calculated also. We must admit the existance of Earth expansion process to understand the obtained large value of terrestrial heat producton. The geoneutrino detector with volume more than 5 kT (LENA type) must be constructed to definitely separate between Bulk Silicat Earth model and Hydridic Earth model. In second version of...

  19. Atomistic Potentials for Palladium-Silver Hydrides

    OpenAIRE

    Hale, L. M.; Wong, B. M.; Zimmerman, J. A.; Zhou, X.

    2013-01-01

    New EAM potentials for the ternary palladium-silver-hydrogen system are developed by extending a previously developed palladium-hydrogen potential. The ternary potentials accurately capture the heat of mixing and structural properties associated with solid solution alloys of palladium-silver. Stable hydrides are produced with properties that smoothly transition across the compositions. Additions of silver to palladium are predicted to alter the properties of the hydrides by decreasing the mis...

  20. Influence of hydrides orientation on strain, damage and failure of hydrided zircaloy-4

    International Nuclear Information System (INIS)

    In pressurized water reactors of nuclear power plants, fuel pellets are contained in cladding tubes, made of Zirconium alloy, for instance Zircaloy-4. During their life in the primary water of the reactor (155 bars, 300 C), cladding tubes are oxidized and consequently hydrided. A part of the hydrogen given off precipitates as Zirconium hydrides in the bulk material and embrittles the material. This embrittlement depends on many parameters, among which hydrogen content and orientation of hydrides with respect to the applied stress. This investigation is devoted to the influence of the orientation of hydrides with respect to the applied stress on strain, damage and failure mechanisms. Macroscopic and SEM in-situ ring tensile tests are performed on cladding tube material (unirradiated cold worked stress-relieved Zircaloy-4) hydrided with about 200 and 500 wppm hydrogen, and with different main hydrides orientation: either parallel or perpendicular to the circumferential tensile direction. We get the mechanical response of the material as a function of hydride orientation and hydrogen content and we investigate the deformation, damage and failure mechanisms. In both cases, digital image correlation techniques are used to estimate local and global strain distributions. Neither the tensile stress-strain response nor the global and local strain modes are significantly affected by hydrogen content or hydride orientation, but the failure modes are strongly modified. Indeed, only 200 wppm radial hydrides embrittle Zy-4: sample fail in the elastic domain at about 350 MPa before strain bands could develop; whereas in other cases sample reach at least 750 MPa before necking and final failure, in ductile or brittle mode. To model this particular heterogeneous material behavior, a non-coupled damage approach which takes into account the anisotropic distribution of the hydrides is proposed. Its parameters are identified from the macroscopic strain field measurements and a

  1. Ultrathin, epitaxial cerium dioxide on silicon

    International Nuclear Information System (INIS)

    It is shown that ultrathin, highly ordered, continuous films of cerium dioxide may be prepared on silicon following substrate prepassivation using an atomic layer of chlorine. The as-deposited, few-nanometer-thin Ce2O3 film may very effectively be converted at room temperature to almost fully oxidized CeO2 by simple exposure to air, as demonstrated by hard X-ray photoemission spectroscopy and X-ray diffraction. This post-oxidation process essentially results in a negligible loss in film crystallinity and interface abruptness

  2. Ultrathin, epitaxial cerium dioxide on silicon

    OpenAIRE

    Flege, Jan Ingo; Kaemena, Björn; Höcker, Jan; Bertram, Florian; Wollschläger, Joachim; Schmidt, Thomas; Falta, Jens

    2014-01-01

    It is shown that ultrathin, highly ordered, continuous films of cerium dioxide may be prepared on silicon following substrate prepassivation using an atomic layer of chlorine. The as-deposited, few-nanometer-thin Ce2O3 film may very effectively be converted at room temperature to almost fully oxidized CeO2 by simple exposure to air, as demonstrated by hard X-ray photoemission spectroscopy and X-ray diffraction. This post-oxidation process essentially results in a negligible loss in film cryst...

  3. Radiative lifetimes of singly ionized cerium

    International Nuclear Information System (INIS)

    Radiative lifetimes accurate to ±5% have been measured for 74 levels in Ce II using time-resolved laser-induced fluorescence on a slow beam of cerium ions. The 17 odd-parity and 57 even-parity levels studied here lie in the energy range 24 000-36 000 cm-1. This new set of lifetimes in Ce II is substantially more extensive than previously published sets, to which a detailed comparison is made. The present lifetime results will provide the absolute calibration for a very large set of measured transition probabilities for Ce II. These are needed for research in astrophysics and lighting

  4. Radiative lifetimes of singly ionized cerium

    Energy Technology Data Exchange (ETDEWEB)

    Hartog, E A Den; Lawler, J E [Department of Physics, University of Wisconsin, Madison, WI 53706 (United States)], E-mail: eadenhar@wisc.edu, E-mail: jelawler@wisc.edu

    2008-02-28

    Radiative lifetimes accurate to {+-}5% have been measured for 74 levels in Ce II using time-resolved laser-induced fluorescence on a slow beam of cerium ions. The 17 odd-parity and 57 even-parity levels studied here lie in the energy range 24 000-36 000 cm{sup -1}. This new set of lifetimes in Ce II is substantially more extensive than previously published sets, to which a detailed comparison is made. The present lifetime results will provide the absolute calibration for a very large set of measured transition probabilities for Ce II. These are needed for research in astrophysics and lighting.

  5. Crystal structure of cerium(4) - dicesium trisulfate

    International Nuclear Information System (INIS)

    Cerium(4) - dicesium trisulfate is investigated by the X-ray diffraction method. Parameters of a monoclinic cell equal: a = 9.772(2), b = 16.797(2), c = 14.812(1)A, β 96.40(1), sp.gr. P21. The structure is formed by interchanging of anion [Ce4(SO4)128-]∞ and cation (Cs+) layers arranged parallel (101). Atoms Ce and Cs are arranged according to the law of a cubic close packing. Coordination polyhedron Ce1 and Ce2 is the two-hat trigonal prism, nine vertices Ce3 and Ce4 are one-hat antiprism

  6. gamma-Zr-Hydride Precipitate in Irradiated Massive delta- Zr-Hydride

    DEFF Research Database (Denmark)

    Warren, M. R.; Bhattacharya, D. K.

    1975-01-01

    During examination of A Zircaloy-2-clad fuel pin, which had been part of a test fuel assembly in a boiling water reactor, several regions of severe internal hydriding were noticed in the upper-plenum end of the pin. Examination of similar fuel pins has shown that hydride of this type is caused by...

  7. Photodissociation of Cerium Oxide Nanocluster Cations.

    Science.gov (United States)

    Akin, S T; Ard, S G; Dye, B E; Schaefer, H F; Duncan, M A

    2016-04-21

    Cerium oxide cluster cations, CexOy(+), are produced via laser vaporization in a pulsed nozzle source and detected with time-of-flight mass spectrometry. The mass spectrum displays a strongly preferred oxide stoichiometry for each cluster with a specific number of metal atoms x, with x ≤ y. Specifically, the most prominent clusters correspond to the formula CeO(CeO2)n(+). The cluster cations are mass selected and photodissociated with a Nd:YAG laser at either 532 or 355 nm. The prominent clusters dissociate to produce smaller species also having a similar CeO(CeO2)n(+) formula, always with apparent leaving groups of (CeO2). The production of CeO(CeO2)n(+) from the dissociation of many cluster sizes establishes the relative stability of these clusters. Furthermore, the consistent loss of neutral CeO2 shows that the smallest neutral clusters adopt the same oxidation state (IV) as the most common form of bulk cerium oxide. Clusters with higher oxygen content than the CeO(CeO2)n(+) masses are present with much lower abundance. These species dissociate by the loss of O2, leaving surviving clusters with the CeO(CeO2)n(+) formula. Density functional theory calculations on these clusters suggest structures composed of stable CeO(CeO2)n(+) cores with excess oxygen bound to the surface as a superoxide unit (O2(-)). PMID:27035210

  8. Low soluble cerium compounds in salt melts

    International Nuclear Information System (INIS)

    The behaviour of cerium tungstate NaCe(WO4)2 and cerium phosphate Na3Ce2(PO4)3 in high-temperature salt melts has been investigated. The solubility in the NaCe(WO4)2-NaWO4-NaCl(1) and Na3Ce2(PO4)3-Na2WO4-NaCl(2) systems at 700-800 deg C has been studied. It is shown, that with the increase of the Na2WO4 part in systems (1), (2) the solubility increases in the following way: for NaCe(WO4)2 from 1.3x10-3 m in NaCl melt to 4.9x10-3 m in NaWO4 melt, for Na3Ce2(PO4)3 from 0.4x10-3 m in NaCl melt to 5.7x10-3 m in NaWO4 melt. With an increase in the Na2WO4 part in system (2) the formation of a new phase - NaCe(WO4)2 is observed. The melting enthalpy of NaCe(WO4)2 is 19+-3 kJ/mol

  9. Storage and characterization of the hydrogen in mixed oxides on base of cerium-nickel and zirconium or the aluminium

    International Nuclear Information System (INIS)

    The mixed oxides based on cerium-nickel and zirconium or aluminium are able to store large quantities of hydrogen, To determine nature, reactivity and properties of hydrogen species (spill-over, direct desorption), the solid were studied by different physicochemical techniques in the dried, calcined and partially reduced states: XRD, porosity, TGA, TPR, TPA, TPD, chemical titration and inelastic neutron scattering (INS). Solids are mainly meso-porous with a common pore size at 4 nm, They are constituted of CeO2 phase, Ce-Ni or Ce-Ni-Zr solid solution and of Ni(OH)2 in the dried state and NiO in the calcined state. The Ni species are in various environments and the strong interactions between the cations in solid solution and at different particles interface influence their reducibility and the creation of anionic vacancies. Activation in H2 in temperature is determining for hydrogen storage in the solid while calcination step is not necessary. INS Analyses evidence that the hydrogen species inserted during treatment in H2 are H+(OH-), hydride H- and H* (metallic nickel) species, present in various chemical environments, in particular for hydride species. All kinds of hydrogen species participate to the reaction during the chemical titration in agreement with the proposed hydrogenation mechanism. The study of the adsorption of hydrogen shows that this step is fast and in quantity of the same order as that measured by chemical titration. The direct desorption of H2 is very low, linked to the presence of hydrogen in interaction with metallic nickel (H*-.). Desorption of water is also observed, in parallel, corresponding to the elimination of groups. The hydride species are not desorbed. These various observations allow connecting hydrogen species properties with their localization in the structure and to model active sites. (author)

  10. Bordoni relaxation and magnetic transformation in cerium and cerium-lanthanum alloys

    International Nuclear Information System (INIS)

    The internal friction in pure cerium and cerium-base alloys with 2.5 and 12 weight percent of lanthanum added at temperature ranging from 4.2 deg up to 77 deg K is described. Amplitude-independent internal friction has been measured with an inverse torsion pendulum with a specimen oscillation frequency of 1-30 hz in vacuum not less than 1.10-5 torr. A temperature of the specimen has been determined with a capacitance-type sensor and a gas gauge. A curve showing the dependence of internal friction upon a temperature of pure cerium has two distinct peaks; the first at 12.5 deg K, the second at 45 deg K. The 12.5 deg K peak is accounted for by a transition of antiferromagnetic β-Ce into a paramagnetic state. The 45 deg K peak is a Bordoni maximum. The paper describes an influence of additions, specimen oscillation frequency variations, deformation and annealing upon the peak behaviour. Added lanthanum reduces not only a peak temperature but a height as well. Studies of the 45 deg K peak have shown that its temperature location depends upon the specimen oscillation frequency. As the frequency increases the peak tends to a range of high temperatures which confirms its relaxation nature

  11. Mechanism of corrosion of zirconium hydride and impact of precipitated hydrides on the Zircaloy-4 corrosion behaviour

    International Nuclear Information System (INIS)

    Highlights: • Higher corrosion rate of hydride compared to matrix (Zy4). • Higher oxygen diffusion coefficient through oxide formed on hydride. • Presence of Zr3O phase between hydride and oxide. • Hydrogen from the hydride phase is not integrated in the oxide during the corrosion process. - Abstract: In Pressurized Water Reactors, zirconium hydrides precipitate in the matrix and could increase the oxidation rate of the claddings. To understand their effect, corrosion tests, TEM and μ-XRD analyses have been performed. This work showed that the oxidation rate and the oxygen diffusion coefficient in the oxide formed on massive hydride are much greater than those of Zircaloy-4. Moreover, oxide characterizations indicated an additional phase indexed as the sub-oxide Zr3O between the oxide film and the massive hydride. Finally, the hydrogen of the hydrides is not incorporated in the oxide during the corrosion process

  12. Preparing Process of Cerium Acetate and Rare Earth Acetate

    Institute of Scientific and Technical Information of China (English)

    Qiao Jun; Ma Ying; Xu Yanhui; Zhang Jun; Chang Shu; Hao Xianku

    2004-01-01

    Preparing process was presented and the influences of concentration of acetic acid, reaction temperature, the ratio of cerium carbonate and acetic acid, heat preservation time to the yield of cerium acetate were discussed.The crystalline cerium acetate and rare earth acetate such as ( La, Ce, Pr, Nd) (Ac) 3, ( Ce, Pr, Nd) (Ac) 3, ( Pr, Nd, Er,Y) (Ac) 3 and yttrium acetate were prepared under this condition.The shape, structure and composition of the crystals were determined by the methods of SEM, TG-DTA, X-ray diffraction and chemical analysis.The optimum prepared conditions of cerium acetate were described.This prepared process has characteristics such as simple process route, low cost, high yield, good quality, no pollution to environment, etc.

  13. Adsorption of Some Hazardous Radionuclides on Cerium(IV) Antimonate

    International Nuclear Information System (INIS)

    Cerium(IV) antimonate had been prepared by the dropwise addition of 0.6 M antimony pentachloride and 0.6 M cerium ammonium nitrate solutions by a molar radio of Ce/Sb 0.75. Exchange isotherms for H+/Co2+ , H+/Cs+, H+/Zn2+ , H+/Sr2+ and H+/Eu3+ have been determined at 25, 40 and 60 degree. Besides it was proved that europium is physically adsorbed while zinc, strontium, cobalt and cesium are chemically adsorbed. Moreover, the heat of adsorption of zinc, strontium, cobalt and cesium on cerium(IV) antimonate had been calculated and indicated that cerium(IV) antimonate is of endothermic behaviour towards these ions. Also the distribution coefficients of these ions were determined and it was found that the selectivity in the order: Eu3+ >Sr2+ > Cs+>Na+

  14. A contribution to the radiologic findings in cerium pneumoconiosis

    International Nuclear Information System (INIS)

    Report on a 69 year old man, who had been employed as photographer in the printing industry and who had been exposed to Cerium for 40 years. The chest X-ray which was performed 9 years after the end of the exposure displayes striate densities of the lungs, which must be considered as a late stage of Cerium-pneumoconiosis. The changes which were found fulfill the code 't 1/0 RO, RM, RU, LO, LM, LU, p 0/1 RO, RM, LO, LM, em, tbu' according to the 'ILO U/C 1971 classification of pneumoconiosis'. The diagnosis could be substantiated by measureing Cerium in the lung parenchyma qualitatively and quantitatively using neutrone activating analysis. The radiolgic findings of the Cerium pneumoconiosis are discussed. (orig.)

  15. Hydrogen storage in complex metal hydrides

    Directory of Open Access Journals (Sweden)

    BORISLAV BOGDANOVIĆ

    2009-02-01

    Full Text Available Complex metal hydrides such as sodium aluminohydride (NaAlH4 and sodium borohydride (NaBH4 are solid-state hydrogen-storage materials with high hydrogen capacities. They can be used in combination with fuel cells as a hydrogen source thus enabling longer operation times compared with classical metal hydrides. The most important point for a wide application of these materials is the reversibility under moderate technical conditions. At present, only NaAlH4 has favourable thermodynamic properties and can be employed as a thermally reversible means of hydrogen storage. By contrast, NaBH4 is a typical non- -reversible complex metal hydride; it reacts with water to produce hydrogen.

  16. Antibacterial Activity of Polymer Coated Cerium Oxide Nanoparticles

    OpenAIRE

    Shah, Vishal; Shah, Shreya; Shah, Hirsh; Rispoli, Fred J.; McDonnell, Kevin T.; Workeneh, Selam; Karakoti, Ajay; Kumar, Amit; Seal, Sudipta

    2012-01-01

    Cerium oxide nanoparticles have found numerous applications in the biomedical industry due to their strong antioxidant properties. In the current study, we report the influence of nine different physical and chemical parameters: pH, aeration and, concentrations of MgSO4, CaCl2, KCl, natural organic matter, fructose, nanoparticles and Escherichia coli, on the antibacterial activity of dextran coated cerium oxide nanoparticles. A least-squares quadratic regression model was developed to underst...

  17. Cerium intermetallics CeTX. Review III

    International Nuclear Information System (INIS)

    The structure-property relationships of CeTX intermetallics with structures other than the ZrNiAl and TiNiSi type are systematically reviewed. These CeTX phases form with electron-poor and electron-rich transition metals (T) and X = Mg, Zn, Cd, Hg, Al, Ga, In, Tl, Si, Ge, Sn, Pb, P, As, Sb, and Bi. The review focusses on the crystal chemistry, the chemical bonding peculiarities, and the magnetic and transport properties. Furthermore 119Sn Moessbauer spectroscopic data, high-pressure studies, hydrogenation reactions and the formation of solid solutions are reviewed. This paper is the third of a series of four reviews on equiatomic intermetallic cerium compound [Part I: R. Poettgen, B. Chevalier, Z. Naturforsch. 2015, 70b, 289; Part II: R. Poettgen, B. Chevalier, Z. Naturforsch. 2015, 70b, 695].

  18. Cerium fluoride crystals for calorimetry at LHC

    International Nuclear Information System (INIS)

    High-resolution homogeneous calorimetry is fully justified for part of the physics program at the Large Hadron Collider (LHC). The main design features of proposed CeF3 crystals for calorimetry for LHC are discussed. The severe constraints LHC imposes on detectors make the use of 'classical' crystals impossible. Therefore, a large R and D effort has been undertaken by the 'Crystal Clear' collaboration in order to find new, dense, fast and radiation hard crystals. A good candidate, cerium fluoride, has been identified and studied. It is interesting at this stage to review the specifications of scintillators for LHC and to see how well available data on CeF3 luminescence, decay time, light yield, optical transmission and resistance to radiation meet them. Milestones to reach before starting a large scale crystal production in view of the eventual construction of a calorimeter, are also discussed. (author) 15 refs., 15 figs., 1 tab

  19. Further results on cerium fluoride crystals

    International Nuclear Information System (INIS)

    A systematic investigation of the properties of cerium fluoride monocrystals has been performed by the 'Crystal Clear' collaboration in view of a possible use of such crystals for the construction of high precision electromagnetic calorimeters for the future generation of high luminosity accelerators. A large sample of different crystals grown by several producers has been studied. The spectroscopic characteristics, the transmission, luminescence and excitation spectra and the decay time curves are analysed. The light yield of the different crystals is measured with photomultipliers and Si photodiodes and compared to reference standards like BGO and NaI(Tl). The radiation damage behaviour is then presented for γ and neutron irradiations, at different doses and dose rates, including thermal and optical bleaching. (orig.)

  20. Further results on cerium fluoride crystals

    Energy Technology Data Exchange (ETDEWEB)

    Anderson, S.; Auffray, E.; Aziz, T.; Baccaro, S.; Banerjee, S.; Bareyre, P.; Barone, L.E.; Borgia, B.; Boutet, D.; Burq, J.P.; Chemarin, M.; Chipaux, R.; Dafinei, I.; D' Atanasio, P.; De Notaristefani, F.; Dezillie, B.; Dujardin, C.; Dutta, S.; Faure, J.L.; Fay, J.; Ferrere, D.; Francescangeli, O.; Fuchs, B.A.; Ganguli, S.N.; Gillespie, G.; Goyot, M.; Gupta, S.K.; Gurtu, A.; Heck, J.; Herve, A.; Hillemanns, H.; Holdener, F.; Ille, B.; Joensson, L.; Kierstead, J.; Krenz, W.; Kway, W.; Le Goff, J.M.; Lebeau, M.; Lebrun, P.; Lecoq, P.; Lemoigne, Y.; Loomis, G.; Lubelsmeyer, K.; Madjar, N.; Majni, G.; El Mamouni, H.; Mangla, S.; Mares, J.A.; Martin, J.P.; Mattioli, M.; Mauger, G.J.; Mazumdar, K.; Mengucci, P.; Merlo, J.P.; Moine, B.; Nikl, N.; Pansart, J.P.; Pedrini, C.; Poinsignon, J.; Polak, K.; Raghavan, R.; Rebourgeard, P.; Rinaldi, D.; Rosa, J.; Rosowsky, A.; Sahuc, P.; Samsonov, V.; Sarkar, S.; Schegelski, V.; Schmitz, D.; Schneegans, M.; Seliverstov, D.; Stoll, S.; Sudhakar, K.; Sven; Crystal Clear Collaboration

    1993-08-15

    A systematic investigation of the properties of cerium fluoride monocrystals has been performed by the 'Crystal Clear' collaboration in view of a possible use of such crystals for the construction of high precision electromagnetic calorimeters for the future generation of high luminosity accelerators. A large sample of different crystals grown by several producers has been studied. The spectroscopic characteristics, the transmission, luminescence and excitation spectra and the decay time curves are analysed. The light yield of the different crystals is measured with photomultipliers and Si photodiodes and compared to reference standards like BGO and NaI(Tl). The radiation damage behaviour is then presented for [gamma] and neutron irradiations, at different doses and dose rates, including thermal and optical bleaching. (orig.)

  1. Mechanical and Thermophysical Properties of Cerium Monopnictides

    Science.gov (United States)

    Bhalla, Vyoma; Singh, Devraj; Jain, S. K.

    2016-03-01

    The ultrasonic attenuation due to phonon-phonon interaction, thermoelastic relaxation and dislocation damping mechanisms has been investigated in cerium monopnictides CeX (X: N, P, As, Sb and Bi) for longitudinal and shear waves along {linearity parameters, Zener anisotropy, ultrasonic velocity, ultrasonic Grüneisen parameter, thermal relaxation time, acoustic coupling constants and ultrasonic attenuation. The fracture/toughness ratio is less than 1.75, which shows that the chosen materials are brittle in nature as found for other monopnictides. The drag coefficient acting on the motion of screw and edge dislocations due to shear and compressional phonon viscosities of the lattice have also been evaluated for both the longitudinal and shear waves. The thermoelastic loss and dislocation damping loss are negligible in comparison to loss due to Akhieser damping (phonon-phonon interaction). The obtained results for CeX are in qualitative agreement with other semi-metallic monopnictides.

  2. Cerium intermetallics CeTX. Review III

    Energy Technology Data Exchange (ETDEWEB)

    Poettgen, Rainer; Janka, Oliver [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie; Chevalier, Bernard [Bordeaux Univ., Pessac (France). Inst. de Chimie de la Matiere Condensee de Bordeaux

    2016-05-01

    The structure-property relationships of CeTX intermetallics with structures other than the ZrNiAl and TiNiSi type are systematically reviewed. These CeTX phases form with electron-poor and electron-rich transition metals (T) and X = Mg, Zn, Cd, Hg, Al, Ga, In, Tl, Si, Ge, Sn, Pb, P, As, Sb, and Bi. The review focusses on the crystal chemistry, the chemical bonding peculiarities, and the magnetic and transport properties. Furthermore {sup 119}Sn Moessbauer spectroscopic data, high-pressure studies, hydrogenation reactions and the formation of solid solutions are reviewed. This paper is the third of a series of four reviews on equiatomic intermetallic cerium compound [Part I: R. Poettgen, B. Chevalier, Z. Naturforsch. 2015, 70b, 289; Part II: R. Poettgen, B. Chevalier, Z. Naturforsch. 2015, 70b, 695].

  3. Comparison of Titration ICP and XRF Spectrometry Methods in Determination of Cerium in Lens Polishing Powder

    International Nuclear Information System (INIS)

    Three analytical methods in determination of cerium in cerium oxide separated from monazite ore for producing lens polishing powder were compared. These methods are titration ICP and XRF spectrometry techniques. The cerium oxide sample with estimated 45% cerium content needed to be digested and converted into solution before the analysis. The analytical results shown significantly no difference between each method. However, the titration method was found to be more convenient and suitable for quality control in the production of cerium oxide as it does not require standard cerium and the complicated analytical instruments

  4. The versatility of hydride-forming materials

    International Nuclear Information System (INIS)

    Full text: Already in 1866 it was realised by Graham that large amounts of hydrogen gas were, as he called it, occluded in pure metallic palladium. Even after more than one century of research in the field of hydrogen storage materials this area is still of great interest. This is not only due to the present-day commercial importance of rechargeable Nickel-Metal Hydride (NiMH) batteries, in which hydride-forming intermetallic materials are widely exploited, but also from a fundamental point of view where new discoveries are still being made. In this review these two areas will be highlighted on the basis of two illustrative examples. The first example relates to the application of hydride-forming bulk materials as electrodes in NiMH batteries. Several hydride-forming compounds are, in principle, available to be used as energy storage electrode material. It turned out, however, that AB5 -type compounds are most successfully applied due to their excellent electrode properties, like high storage capacity, rate capability and rapid electrode activation. Another important aspect is the electrode stability during cycling, which determines the battery cycle life. By designing multicomponent AB5 compounds it has been shown that this stability can be drastically improved. Recently, a second class of very stable compounds has been proposed. These so-called non-stoichiometric AB5+x compounds are characterised by the fact that the severe particle size reduction, always accompanying the hydride-formation process, is reduced. The stability mechanism responsible for this remarkable behaviour will be outlined. The second example relates to thin film applications. Recently, it has been found that the electronic conductivity of thin films composed of rare earth metal hydrides like, for example, yttrium hydride and gadolinium hydride, changes dramatically from metallic in the dihydride state to semiconducting in the trihydride state. In line with these conductivity changes the

  5. Stress induced reorientation of vanadium hydride

    Energy Technology Data Exchange (ETDEWEB)

    Beardsley, M. B.

    1977-10-01

    The critical stress for the reorientation of vanadium hydride was determined for the temperature range 180/sup 0/ to 280/sup 0/K using flat tensile samples containing 50 to 500 ppM hydrogen by weight. The critical stress was observed to vary from a half to a third of the macroscopic yield stress of pure vanadium over the temperature range. The vanadium hydride could not be stress induced to precipitate above its stress-free precipitation temperature by uniaxial tensile stresses or triaxial tensile stresses induced by a notch.

  6. Automotive cooling systems based on metal hydrides

    OpenAIRE

    Linder, Marc

    2010-01-01

    The present work focuses on metal hydride sorption systems as an alternative technology for automotive air-conditioning systems. Although this technology offers the possibility to increase the energy efficiency of a car (by utilising waste heat) and consequently reduces the CO2 emissions, its weight specific cooling power has so far been the main obstacle for an automotive application. Based on investigations of various metal hydrides, two alloys (LmNi4.91Sn0.15 and Ti0.99Zr0.01V0.43Fe0.09Cr0...

  7. Effects of δ-hydride precipitation at a crack tip on crack propagation in delayed hydride cracking of Zircaloy-2

    International Nuclear Information System (INIS)

    Highlights: • Steady state crack velocity of delayed hydride cracking in Zircaloy-2 was analyzed. • A large stress peak is induced at an end of hydride by volume expansion of hydride. • Hydrogen diffuses to the stress peak, thereby accelerating steady hydride growth. • Crack velocity was estimated from the calculated hydrogen flux into the stress peak. • There was good agreement between calculation results and experimental data. -- Abstract: Delayed hydride cracking (DHC) of Zircaloy-2 is one possible mechanism for the failure of boiling water reactor fuel rods in ramp tests at high burnup. Analyses were made for hydrogen diffusion around a crack tip to estimate the crack velocity of DHC in zirconium alloys, placing importance on effects of precipitation of δ-hydride. The stress distribution around the crack tip is significantly altered by precipitation of hydride, which was strictly analyzed using a finite element computer code. Then, stress-driven hydrogen diffusion under the altered stress distribution was analyzed by a differential method. Overlapping of external stress and hydride precipitation at a crack tip induces two stress peaks; one at a crack tip and the other at the front end of the hydride precipitate. Since the latter is larger than the former, more hydrogen diffuses to the front end of the hydride precipitate, thereby accelerating hydride growth compared with that in the absence of the hydride. These results indicated that, after hydride was formed in front of the crack tip, it grew almost steadily accompanying the interaction of hydrogen diffusion, hydride growth and the stress alteration by hydride precipitation. Finally, crack velocity was estimated from the calculated hydrogen flux into the crack tip as a function of temperature, stress intensity factor and material strength. There was qualitatively good agreement between calculation results and experimental data

  8. Effect of yttrium on nucleation and growth of zirconium hydrides

    International Nuclear Information System (INIS)

    Addition of yttrium in zirconium causes precipitates of yttrium, which form two types of particles and are oxidized upon heat treatment. One type of particles with sub-micrometer scale sizes has a low population, whereas the other with nano scale sizes has a high population and cluster distribution. Owing to strong affinity of yttrium to hydrogen, the nanoparticles, mostly within the grains of the Zr–Y alloy, attract nucleation of hydrides at the clusters of the nanoparticles and cause preferential distribution of intragranular hydrides. In comparison with that of Zr, additional nanoparticles in the Zr–Y alloy impede further growth of hydride precipitates during hydriding. It is deduced that the impediment of growing hydride precipitates by the nanoparticles is developed during an auto-catalytic nucleation process, which leads to formation of thin and intragranular hydrides, favorable to mitigation of hydride embrittlement

  9. Effect of yttrium on nucleation and growth of zirconium hydrides

    Energy Technology Data Exchange (ETDEWEB)

    Li, Changji; Xiong, Liangyin; Wu, Erdong; Liu, Shi, E-mail: sliu@imr.ac.cn

    2015-02-15

    Addition of yttrium in zirconium causes precipitates of yttrium, which form two types of particles and are oxidized upon heat treatment. One type of particles with sub-micrometer scale sizes has a low population, whereas the other with nano scale sizes has a high population and cluster distribution. Owing to strong affinity of yttrium to hydrogen, the nanoparticles, mostly within the grains of the Zr–Y alloy, attract nucleation of hydrides at the clusters of the nanoparticles and cause preferential distribution of intragranular hydrides. In comparison with that of Zr, additional nanoparticles in the Zr–Y alloy impede further growth of hydride precipitates during hydriding. It is deduced that the impediment of growing hydride precipitates by the nanoparticles is developed during an auto-catalytic nucleation process, which leads to formation of thin and intragranular hydrides, favorable to mitigation of hydride embrittlement.

  10. Metal hydrides for hydrogen storage in nickel hydrogen batteries

    International Nuclear Information System (INIS)

    Metal hydride hydrogen storage in nickel hydrogen (Ni/H2) batteries has been shown to increase battery energy density and improve battery heat management capabilities. However the properties of metal hydrides in a Ni/H2 battery environment, which contains water vapor and oxygen in addition to the hydrogen, have not been well characterized. This work evaluates the use of hydrides in Ni/H2 batteries by fundamental characterization of metal hydride properties in a Ni/H2 cell environment. Hydrogen sorption properties of various hydrides have been measured in a Ni/H2 cell environment. Results of detailed thermodynamic and kinetic studies of hydrogen sorption in LaNi5 in a Ni/H2 cell environment are presented. Long-term cycling studies indicate that degradation of the hydride can be minimized by cycling between certain pressure limits. A model describing the mechanism of hydride degradation is presented

  11. Are RENiAl hydrides metallic?

    Czech Academy of Sciences Publication Activity Database

    Eichinger, K.; Havela, L.; Prokleška, J.; Stelmakhovych, O.; Daniš, S.; Šantavá, Eva; Miliyanchuk, K.

    2009-01-01

    Roč. 100, č. 9 (2009), s. 1200-1202. ISSN 1862-5282 Grant ostatní: GA ČR(CZ) GA202/07/0418 Institutional research plan: CEZ:AV0Z10100520 Keywords : rare earth metals * magnetism * hydrides Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 0.862, year: 2009

  12. Computational study of metal hydride cooling system

    Energy Technology Data Exchange (ETDEWEB)

    Satheesh, A.; Muthukumar, P.; Dewan, Anupam [Department of Mechanical Engineering, Indian Institute of Technology, Guwahati, Guwahati 781039 (India)

    2009-04-15

    A computational study of a metal hydride cooling system working with MmNi{sub 4.6}Al{sub 0.4}/MmNi{sub 4.6}Fe{sub 0.4} hydride pair is presented. The unsteady, two-dimensional mathematical model in an annular cylindrical configuration is solved numerically for predicting the time dependent conjugate heat and mass transfer characteristics between coupled reactors. The system of equations is solved by the fully implicit finite volume method (FVM). The effects of constant and variable wall temperature boundary conditions on the reaction bed temperature distribution, hydrogen concentration, and equilibrium pressures of the reactors are investigated. A dynamic correlation of the pressure-concentration-temperature plot is presented. At the given operating temperatures of 363/298/278 K (T{sub H}/T{sub M}/T{sub C}), the cycle time for the constant and variable wall temperature boundary conditions of a single-stage and single-effect metal hydride system are found to be 1470.0 s and 1765.6 s, respectively. The computational results are compared with the experimental data reported in the literature for LaNi{sub 4.61}Mn{sub 0.26}Al{sub 0.13}/La{sub 0.6}Y{sub 0.4}Ni{sub 4.8}Mn{sub 0.2} hydride pair and a good agreement between the two was observed. (author)

  13. Inhibition of pH fronts in corrosion cells due to the formation of cerium hydroxide

    NARCIS (Netherlands)

    Soestbergen, M. van; Erich, S.J.F.; Huinink, H.P.; Adan, O.C.G.

    2013-01-01

    The effect of cerium-based corrosion inhibitors on the pH front between the alkaline cathode and acidic anode in corrosion cells has been studied. The cerium component of these inhibitors can affect the pH front since it precipitates in an alkaline environment as cerium hydroxide, which is important

  14. Cerium as a Surrogate in the Plutonium Immobilized Form

    International Nuclear Information System (INIS)

    The Department of Energy (DOE) plans to immobilize a portion of the excess weapons useable plutonium in a ceramic form for final geologic disposal. The proposed immobilization form is a titanate based ceramic consisting primarily of a pyrochlore phase with lesser amounts of brannerite, rutile, zirconolite, vitreous phases and/or other minor phases depending on the impurities present in the feed. The ceramic formulation is cold-pressed and then densified via a reactive sintering process. Cerium has been used as a surrogate for plutonium to facilitate formulation development and process testing. The use of cerium vs. plutonium results in differences in behavior during sintering of the ceramic form. The phase development progression and final phase assemblage is different when cerium is substituted for the actinides in the form. However, the physical behavior of cerium oxide powder and the formation of a pyrochlore-rich ceramic of similar density to the actinide-bearing material make cerium an adequate surrogate for formulation and process development studies

  15. Electrodeposited cerium film as chromate replacement for tinplate

    International Nuclear Information System (INIS)

    The cerium film was prepared on tinplate by electrodeposition method. Sulfide-stain resistance of the Ce-passivated, unpassivated and Cr-passivated tinplates was evaluated using a cysteine tarnish test. Corrosion behavior of these tinplates in contact with 3.5% NaCl solution and 0.1 M citric-citrate buffer solution was investigated using Tafel measurement and electrochemical impedance spectroscopy measurement, respectively. The adhesion of epoxyphenolic lacquer to the Ce-passivated tinplate was checked using a cross hatch cutter. The morphology, composition and thickness of the cerium film were studied by atomic force microscopy, X-ray photoelectron spectroscopy and X-ray fluorescence spectrometry. According to the results, the Ce-passivated tinplate shows the best sulfide-stain resistance and the best corrosion protection property compared with the unpassivated and Cr-passivated tinplates. The adhesion of epoxyphenolic lacquer to the Ce-passivated tinplate is good. The cerium film is composed of the closely packed particles of about 50-200 nm in diameter. The film mainly consists of cerium and oxygen, which mainly exist as CeO2, Ce2O3 and their hydrates such as Ce(OH)4, Ce(OH)3. The total cerium amount of the film is about 0.110 g/m2

  16. Potential for recovery of cerium contained in automotive catalytic converters

    Science.gov (United States)

    Bleiwas, Donald I.

    2013-01-01

    Catalytic converters (CATCONs) are required by Federal law to be installed in nearly all gasoline- and diesel-fueled onroad vehicles used in the United States. About 85 percent of the light-duty vehicles and trucks manufactured worldwide are equipped with CATCONs. Portions of the CATCONs (called monoliths) are recycled for their platinum-group metal (PGM) content and for the value of the stainless steel they contain. The cerium contained in the monoliths, however, is disposed of along with the slag produced from the recycling process. Although there is some smelter capacity in the United States to treat the monoliths in order to recover the PGMs, a great percentage of monoliths is exported to Europe and South Africa for recycling, and a lesser amount is exported to Japan. There is presently no commercial-scale capacity in place domestically to recover cerium from the monoliths. Recycling of cerium or cerium compounds from the monoliths could help ensure against possible global supply shortages by increasing the amount that is available in the supply chain as well as the number and geographic distribution of the suppliers. It could also reduce the amount of material that goes into landfills. Also, the additional supply could lower the price of the commodity. This report analyzes how much cerium oxide is contained in CATCONs and how much could be recovered from used CATCONs.

  17. Characterization of cerium fluoride nanocomposite scintillators

    Energy Technology Data Exchange (ETDEWEB)

    Stange, Sy [Los Alamos National Laboratory; Esch, Ernst I [Los Alamos National Laboratory; Brown, Leif O [Los Alamos National Laboratory; Couture, Aaron J [Los Alamos National Laboratory; Mckigney, Edward A [Los Alamos National Laboratory; Muenchausen, Ross E [Los Alamos National Laboratory; Del Sesto, Rico E [Los Alamos National Laboratory; Gilbertson, Robert D [Los Alamos National Laboratory; Mccleskey, T Mark [Los Alamos National Laboratory; Reifarth, Rene [Los Alamos National Laboratory

    2009-01-01

    Measurement of the neutron capture cross-sections of a number of short-lived isotopes would advance both pure and applied scientific research. These cross-sections are needed for calculation of criticality and waste production estimates for the Advanced Fuel Cycle Initiative, for analysis of data from nuclear weapons tests, and to improve understanding of nucleosynthesis. However, measurement of these cross-sections would require a detector with a faster signal decay time than those used in existing neutron capture experiments. Crystals of faster detector materials are not available in sufficient sizes and quantities to supply these large-scale experiments. Instead, we propose to use nanocomposite detectors, consisting of nanoscale particles of a scintillating material dispersed in a matrix material. We have successfully fabricated cerium fluoride (CeF{sub 3}) nanoparticles and dispersed them in a liquid matrix. We have characterized this scintillator and have measured its response to neutron capture. Results of the optical, structural, and radiation characterization will be presented.

  18. Characterization of cerium fluoride nanocomposite scintillators

    International Nuclear Information System (INIS)

    Measurement of the neutron capture cross-sections of a number of short-lived isotopes would advance both pure and applied scientific research. These cross-sections are needed for calculation of criticality and waste production estimates for the Advanced Fuel Cycle Initiative, for analysis of data from nuclear weapons tests, and to improve understanding of nucleosynthesis. However, measurement of these cross-sections would require a detector with a faster signal decay time than those used in existing neutron capture experiments. Crystals of faster detector materials are not available in sufficient sizes and quantities to supply these large-scale experiments. Instead, we propose to use nanocomposite detectors, consisting of nanoscale particles of a scintillating material dispersed in a matrix material. We have successfully fabricated cerium fluoride (CeF3) nanoparticles and dispersed them in a liquid matrix. We have characterized this scintillator and have measured its response to neutron capture. Results of the optical, structural, and radiation characterization will be presented.

  19. Stabilized zirconia with cerium and neodymium addition

    International Nuclear Information System (INIS)

    Zr0,9 Ce0,05 Nd0,05 O1,975 system was synthesized with the use of the Pechini method. The polymeric resin was calcined at 350 deg C/3 h and analysed by FTIR that show bands relative to organic. Radicals esther type. The TGA curve indicated the polymeric decomposition occurring from 30 deg C to 740 deg C. DTA analysis show a exothermic peak in 100 deg C due to loss of water of material. From 500 deg C to 800 deg C was observed a intense peak due to polymer decomposition and the zirconia crystallization. The calcined powder from 350 deg C/3 h e 30 min to 900 deg/3 h were analysed by XRD that show the crystalline phase formation with the increase of temperature. The X-ray diffraction pattern show the presence of two phases, such as tetragonal and cubic of zirconia demonstrating that neodymium and cerium additions led to zirconia stabilization. (author)

  20. Cerium Dioxide Thin Films Using Spin Coating

    Directory of Open Access Journals (Sweden)

    D. Channei

    2013-01-01

    Full Text Available Cerium dioxide (CeO2 thin films with varying Ce concentrations (0.1 to 0.9 M, metal basis were deposited on soda-lime-silica glass substrates using spin coating. It was found that all films exhibited the cubic fluorite structure after annealing at 500°C for 5 h. The laser Raman microspectroscopy and GAXRD analyses revealed that increasing concentrations of Ce resulted in an increase in the degree of crystallinity. FIB and FESEM images confirmed the laser Raman and GAXRD analyses results owing to the predicted increase in film thickness with increasing Ce concentration. However, porosity and shrinkage (drying cracking of the films also increased significantly with increasing Ce concentrations. UV-VIS spectrophotometry data showed that the transmission of the films decreased with increasing Ce concentrations due to the increasing crack formation. Furthermore, a red shift was observed with increasing Ce concentrations, which resulted in a decrease in the optical indirect band gap.

  1. Chlorination and Carbochlorination of Cerium Oxide

    International Nuclear Information System (INIS)

    The chlorination and carbochlorination of cerium oxide were studied by thermogravimetry under controlled atmosphere (TG) in the 7000C 9500C temperature range.Both reactants and products were analyzed by X-ray diffraction (RX), scanning electronic microscopy (SEM) and energy dispersive spectroscopy (EDS). Thermodynamic calculations were performed by computer assisted software.The chlorination starts at a temperature close to 8000C.This reaction involves the simultaneous formation and evaporation of CeCl3.Both processes control the reaction rate and their kinetic may not be easily separated.The apparent chlorination activation energy in the 8500C-9500C temperature range is 172 to 5 kJ/ mole.Carbon transforms the CeO2-Cl2 into a more reactive system: CeO2-C-Cl2, where the effects of the carbon content, total flow rate and temperature were analyzed.The carbochlorination starting temperature is 7000C.This reaction is completed in one step controlled by mass transfer with an apparent activation energy of 56 to 5 kJ/mole in the 8500C-9500C temperature range

  2. Environmental Geochemistry of Cerium: Applications and Toxicology of Cerium Oxide Nanoparticles

    Directory of Open Access Journals (Sweden)

    Jessica T. Dahle

    2015-01-01

    Full Text Available Cerium is the most abundant of rare-earth metals found in the Earth’s crust. Several Ce-carbonate, -phosphate, -silicate, and -(hydroxide minerals have been historically mined and processed for pharmaceutical uses and industrial applications. Of all Ce minerals, cerium dioxide has received much attention in the global nanotechnology market due to their useful applications for catalysts, fuel cells, and fuel additives. A recent mass flow modeling study predicted that a major source of CeO2 nanoparticles from industrial processing plants (e.g., electronics and optics manufactures is likely to reach the terrestrial environment such as landfills and soils. The environmental fate of CeO2 nanoparticles is highly dependent on its physcochemical properties in low temperature geochemical environment. Though there are needs in improving the analytical method in detecting/quantifying CeO2 nanoparticles in different environmental media, it is clear that aquatic and terrestrial organisms have been exposed to CeO2 NPs, potentially yielding in negative impact on human and ecosystem health. Interestingly, there has been contradicting reports about the toxicological effects of CeO2 nanoparticles, acting as either an antioxidant or reactive oxygen species production-inducing agent. This poses a challenge in future regulations for the CeO2 nanoparticle application and the risk assessment in the environment.

  3. Cerium luminescence in borate glass and effect of aluminium on blue green emission of cerium ions

    International Nuclear Information System (INIS)

    CeO2 doped lead borate (CE) and lead alumino borate (CEA) glasses are prepared by melt quench method at high temperature. The main luminescence band of 5d–4f transition of Ce3+ ions with maxima at around 489 nm of Ce3+ ions in these glasses has been observed, along with red shift and larger stokes shift, which shows that the covalency of the rare earth to oxygen bond increases with the increase in CeO2 content at the expense of Al2O3. Shifting of UV absorption edge towards longer wavelength and a decrease in band gap with increase in CeO2 concentration in both the glass systems has been observed. Moreover densification and stabilization of glass network has been observed which is due to conversion of BO3 units to more compact and stable BO4 units. This covalency effect and the formation of BO4 groups with addition of CeO2 and incorporation of Al2O3 content are responsible for clear effect on luminescence of the present glass system. Moreover the optical basicity values were theoretically determined along with density and molar volume. -- Highlights: • Aluminium incorporation assists in dispersing the clusters of cerium ions and thus enhancing luminescence response. • Decrease of optical band gap energy with an increase of cerium concentration shows the semiconducting behavior. • Larger stokes shift shows that the covalency of rare earth to oxygen bond increases with increase in CeO2

  4. Cerium, manganese and cerium/manganese ceramic monolithic catalysts. Study of VOCs and PM removal

    Institute of Scientific and Technical Information of China (English)

    COLMAN-LERNER Esteban; PELUSO Miguel Andrs; SAMBETH Jorge; THOMAS Horacio

    2016-01-01

    Ceramic supported cerium, manganese and cerium-manganese catalysts were prepared by direct impregnation of aqueous precursor, and characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Brunauer-Emmett-Teller method (BET), temperature programmed reduction (H2-TPR), X-ray photoelectron spectroscopy (XPS) acidity measurements and electrical conductivity. The catalytic activity was evaluated for volatile organic compounds (VOC) (ethanol, methyl ethyl ketone and toluene) oxidation. Additionally, catalysts were tested in particulate matter (PM) combustion. The characterization results indicated that Ce was in the form of Ce4+ and Ce3+, and Mn existed in the form of Mn4+and Mn3+on the surface of the Mn/AC sample and in the form of Mn4+ in the Ce/Mn/AC monolith. VOC oxidation results revealed that the Ce/Mn/AC sample showed an excellent performance compared with ceramic supported CeO2 (Ce/AC) and MnOx (Mn/AC) samples. The PM combustion was also higher on Ce/Mn/AC monoliths. The enhanced catalytic activity was mainly attributed to the Ce and Mn interaction which enhanced the acidity, conductiv-ity and the reducibility of the oxides.

  5. Hydrogen storage in metallic hydrides: the hydrides of magnesium-nickel alloys

    International Nuclear Information System (INIS)

    The massive and common use of hydrogen as an energy carrier requires an adequate solution to the problem of storing it. High pressure or low temperatures are not entirely satisfactory, having each a limited range of applications. Reversible metal hydrides cover a range of applications intermediate to high pressure gas and low temperature liquid hydrogen, retaining very favorable safety and energy density characteristics, both for mobile and stationary applications. This work demonstrates the technical viability of storing hydrogen in metal hydrides of magnesium-nickel alloys. Also, it shows that technology, a product of science, can be generated within an academic environment, of the goal is clear, the demand outstanding and the means available. We review briefly theoretical models relating to metal hydride properties, specially the thermodynamics properties relevant to this work. We report our experimental results on hydrides of magnesium-nickel alloys of various compositions including data on structure, hydrogen storage capacities, reaction kinetics, pressure-composition isotherms. We selected a promising alloy for mass production, built and tested a modular storage tank based on the hydrides of the alloy, with a capacity for storing 10 Nm sup(3) of hydrogen of 1 atm and 20 sup(0)C. The tank weighs 46,3 Kg and has a volume of 21 l. (author)

  6. Elaboration and characterization of thin solid films containing cerium

    Science.gov (United States)

    Hamdi, S.; Guerfi, S.; Siab, R.

    2009-11-01

    Cerium oxide films are widely studied as a promising alternative to Cr(VI) based pre-treatments for the corrosion protection of different metals and alloys. Cathodic electrodeposition of Cerium containing thin films was realised on TA6V substrates from a Ce(NO3)3, 6H2O and mixed water-ethyl alcohol solutions at 0.01 M. Experimental conditions to obtain homogeneous and crack free thin films were determined. The deposited cerium quantity appears proportional to the quantity of electricity used, as indicated by the Faraday law. Subsequent thermal treatment lead to a CeO2 coating, expected to provide an increase of TA6V oxidation resistance at high temperatures. The deposits were characterized by differential scanning calorimetry (DSC), optical and scanning electron microscopies.

  7. Cerium uptake by zeolite A synthesized from natural clinoptilolite tuffs

    International Nuclear Information System (INIS)

    Natural clinoptilolite tuffs from the Semnan region in Iran was used for the synthesis of zeolite A. The tuffs and synthesized zeolites were characterized by XRD and XRF. The sorption behavior of the synthesized zeolite toward cerium was studied. Using the Lagergren's equation, the absorption constant was calculated. The measured distribution coefficient values (Kd) indicated that cerium uptake is higher in lower initial concentrations, higher temperature and higher pH values. Thermodynamic parameters of the exchange were calculated through construction of ion-exchange isotherms at three temperatures of 298, 323 and 343 K. The dynamic absorption of cerium was also studied by passing the solution through a column in the presence and absence of sodium ions. (author)

  8. Metal hydrides based high energy density thermal battery

    International Nuclear Information System (INIS)

    Highlights: • The principle of the thermal battery using advanced metal hydrides was demonstrated. • The thermal battery used MgH2 and TiMnV as a working pair. • High energy density can be achieved by the use of MgH2 to store thermal energy. - Abstract: A concept of thermal battery based on advanced metal hydrides was studied for heating and cooling of cabins in electric vehicles. The system utilized a pair of thermodynamically matched metal hydrides as energy storage media. The pair of hydrides that was identified and developed was: (1) catalyzed MgH2 as the high temperature hydride material, due to its high energy density and enhanced kinetics; and (2) TiV0.62Mn1.5 alloy as the matching low temperature hydride. Further, a proof-of-concept prototype was built and tested, demonstrating the potential of the system as HVAC for transportation vehicles

  9. METHOD OF FABRICATING A URANIUM-ZIRCONIUM HYDRIDE REACTOR CORE

    Science.gov (United States)

    Weeks, I.F.; Goeddel, W.V.

    1960-03-22

    A method is described of evenly dispersing uranlum metal in a zirconium hydride moderator to produce a fuel element for nuclear reactors. According to the invention enriched uranium hydride and zirconium hydride powders of 200 mesh particle size are thoroughly admixed to form a mixture containing 0.1 to 3% by weight of U/sup 235/ hydride. The mixed powders are placed in a die and pressed at 100 tons per square inch at room temperature. The resultant compacts are heated in a vacuum to 300 deg C, whereby the uranium hydride deoomposes into uranium metal and hydrogen gas. The escaping hydrogen gas forms a porous matrix of zirconium hydride, with uramum metal evenly dispersed therethrough. The advantage of the invention is that the porosity and uranium distribution of the final fuel element can be more closely determined and controlled than was possible using prior methods of producing such fuel ele- ments.

  10. SANS Measurement of Hydrides in Uranium

    International Nuclear Information System (INIS)

    SANS scattering is shown to be an effective method for detecting the presence of hydrogen precipitates in uranium. High purity polycrystalline samples of depleted uranium were given several hydriding treatments which included extended exposures to hydrogen gas at two different pressures at 630 C as well as a furnace anneal at 850 C followed by slow cooling in the near absence hydrogen gas. All samples exhibited neutron scattering that was in proportion to the expected levels of hydrogen content. While the scattering signal was strong, the shape of the scattering curve indicated that the scattering objects were large sized objects. Only by use of a very high angular resolution SANS technique was it possible to make estimates of the major diameter of the scattering objects. This analysis permits an estimate of the volume fraction and means size of the hydride precipitates in uranium

  11. NMR investigations of YMn2Hx hydrides

    International Nuclear Information System (INIS)

    The YMn2Hx hydrides with x = 1, 2, 3 were investigated by 55Mn NMR spin echo measurements at atmospheric and high pressure. Resonance lines at frequencies up to 440 MHz were observed for the hydrides, corresponding to a huge increase of the hyperfine fields at those Mn with hydrogen neighbours. At high pressure the initial decrease of the magnitude of the Mn hyperfine field of YMn2H1 at 4.2 K was found to be 4% per kbar which is an order of magnitude bigger than observed in the other magnetically ordered materials. The effects are interpreted in terms of changes of the orbital contribution and valence electron contribution to the hyperfine field caused by hydrogenation and the influence of the external pressure. (orig.)

  12. The electrochemical impedance of metal hydride electrodes

    DEFF Research Database (Denmark)

    Valøen, Lars Ole; Lasia, Andrzej; Jensen, Jens Oluf;

    2002-01-01

    The electrochemical impedance responses for different laboratory type metal hydride electrodes were successfully modeled and fitted to experimental data for AB5 type hydrogen storage alloys as well as one MgNi type electrode. The models fitted the experimental data remarkably well. Several AC......, explaining the experimental impedances in a wide frequency range for electrodes of hydride forming materials mixed with copper powder, were obtained. Both charge transfer and spherical diffusion of hydrogen in the particles are important sub processes that govern the total rate of the electrochemical...... hydrogen absorption/desorption reaction. To approximate the experimental data, equations describing the current distribution in porous electrodes were needed. Indications of one or more parallel reduction/oxidation processes competing with the electrochemical hydrogen absorption/desorption reaction were...

  13. Synthesis of metal hydrides by cold rolling

    International Nuclear Information System (INIS)

    'Full text:' In the development of metal hydrides for commercial applications, a special attention should be devoted to the ways of production. For commercial success, the raw elements of the hydrogen storage materials should be of low cost, the synthesis process should be inexpensive and easily scalable. Therefore, it is important to put some effort on the elaboration of new and more efficient means of producing metal hydrides. In this perspective, cold rolling was investigated as a new means of producing nanocrystalline materials. This technique is well-known in the industry and easily scalable. Cold rolling was performed on Mg-Ni system. The evolution of morphology, crystal structure, crystallite size, deformation, and preferred orientation was studied as a function of number of rolling passes. Cold rolling followed by a heat treatment produced the intermetallic Mg2Ni. Without heat treatment and for a large number of rolling, an amorphous phase was synthesized. (author)

  14. Numerical study of a magnesium hydride tank

    Science.gov (United States)

    Delhomme, Baptiste; de Rango, Patricia; Marty, Philippe

    2012-11-01

    Hydrogen storage in metal hydride tanks (MHT) is a very promising solution. Several experimental tanks, studied by different teams, have already proved the feasibility and the interesting performances of this solution. However, in much cases, an optimization of tank geometry is still needed in order to perform fast hydrogen loading. The development of efficient numerical tools is a key issue for MHT design and optimization. We propose a simple model representing a metal hydride tank exchanging its heat of reaction with a thermal fluid flow. In this model, the radial and axial discretisations have been decoupled by using Matlab® one-dimensional tools. Calculations are compared to experimental results obtained in a previous study. A good agreement is found for the loading case. The discharging case shows some discrepancies, which are discussed in this paper.

  15. The hydride fluoride crystal structure database, HFD

    Energy Technology Data Exchange (ETDEWEB)

    Gingl, F.; Gelato, L.; Yvon, K. [Geneva Univ. (Switzerland). Lab. Crystallographie aux Rayons X

    1997-05-20

    HFD is a new data base containing crystal structure information on more than one thousand metal hydrides and fluorides. It includes space group, cell parameters, standardized atom positions, site occupancies and references. The compilation is critical as only refined crystal structures are considered and the data are checked for internal consistency. It is comprehensive as structural information is extracted from all major scientific journals, and it is continuously updated. HFD can be searched according to various criteria such as symmetry, chemical elements, composition etc. The primary motivation for creating HFD was to predict new metal hydrides and to study their structural analogies with metal fluorides. However, HFD can also be used for other applications such as the simulation of diffraction patterns and the drawing of crystal structures. (orig.) 13 refs.

  16. Synthesis and characterization of magnesium doped cerium oxide for the fuel cell application

    Science.gov (United States)

    Kumar, Amit; Kumari, Monika; Kumar, Mintu; Kumar, Sacheen; Kumar, Dinesh

    2016-05-01

    Cerium oxide has attained much attentions in global nanotechnology market due to valuable application for catalytic, fuel additive, and widely as electrolyte in solid oxide fuel cell. Doped cerium oxide has large oxygen vacancies that allow for greater reactivity and faster ion transport. These properties make cerium oxide suitable material for SOFCs application. Cerium oxide electrolyte requires lower operation temperature which shows improvement in processing and the fabrication technique. In our work, we synthesized magnesium doped cerium oxide by the co-precipitation method. With the magnesium doping catalytic reactivity of CeO2 was increased. Synthesized nanoparticle were characterized by the XRD and UV absorption techniques.

  17. Speciesion arsenic and selenium using hydride method atomic absorption spectroscopy

    International Nuclear Information System (INIS)

    Hydrides production - atomic absorption spectroscopy system was studied. Hydrides production tool and gas-liquid separator were tested and successfully used in this work. Hydride was produced through natrium borohydride reaction with sample solution. Emitted gas was separated by gas-liquid separator before it is carried by nitrogen gas through T tube which is put in atomic absorption flame spectrophotometer. Efficiency of the system was tested through standard reference sample and seawater / sediment samples which is collected from Negeri Johor water bays

  18. The PL "violet shift" of cerium dioxide on silicon

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    CeO2 thin film was fabricated by dual ion beam epitaxial technique. The phenomenon of PL violet shift at room temperature was observed, and the distance of shift was about 65 nm. After the analysis of crystal structure and valence in the compound were carried out by XRD and XPS technique, it was concluded that the PL shift was related with valence of cerium ion in the oxides. When the valence of cerium ion varied from tetravalence to trivalence, the PL peak position would move from blue region to violet region and the phenomenon of "violet shift" was observed.

  19. Photo-assisted reduction in nanostructured cerium-based coatings

    International Nuclear Information System (INIS)

    Nanostructured cerium-based coatings on AZ31 Mg alloy substrates exposed to sunlight under ambient conditions had an ∼30% increase in Ce(III) species compared to unexposed coatings as measured by X-ray photoelectron spectroscopy. A decrease in film cracks and shift in bandgap from 2.5 eV to 2.7 eV were also measured. Visible changes in color, from yellow to translucent, with exposure were also observed and suggest that cerium-based coatings are reduced by light exposure in humid environments

  20. Membrane assisted liquid-liquid extraction of cerium

    International Nuclear Information System (INIS)

    Membrane assisted liquid-liquid extraction of cerium was investigated, with emphasis placed on the study of the reaction chemistry and the kinetics of non-dispersive solvent extraction and stripping with microporous membranes. A bulk liquid membrane process was developed for the purification of cerium(IV) from sulfate solutions containing other rare earth elements. The cerium process was studied in both a flat sheet contained liquid membrane configuration and with hollow fibre contactors. Di-2-ethylhexyl phosphoric acid (DEHPA) was identified as a suitable extractant for cerium(IV) from sulfuric acid solution, with due consideration of factors such as extraction ability, resistance to degradation, solvent selectivity and potential for sulfate transfer into a strip solution. A detailed study of the extraction of cerium(IV) with DEHPA defined the extraction reaction chemistry. The Ce/DEHPA/sulfate system was also investigated with a flat sheet bulk liquid membrane configuration, using both sulfuric and hydrochloric acid as receiver solutions. These tests identified that hydrophobic membranes provide better mass transfer for extraction and hydrophilic membranes are better for stripping. The presence of an impurity, mono 2-ethylhexyl phosphoric acid (MEHPA), was found to have a dramatic accelerating effect on the rate of the chemical extraction reaction. This was attributed to its higher interfacial activity and population compared to DEHPA, and the fact that MEHPA was also found to be an active carrier for cerium(IV). The mass transfer rate of membrane assisted extraction and stripping of cerium, using hydrophobic and hydrophilic microporous membranes, respectively, was investigated using a modified Lewis-type cell. It was quantitatively demonstrated that the extraction process was mainly controlled by membrane diffusion and the stripping process was controlled by the chemical reaction rate, with membrane diffusion becoming important at low distribution coefficients

  1. Optical and electrical studies of cerium mixed oxides

    Energy Technology Data Exchange (ETDEWEB)

    Sherly, T. R., E-mail: trsherly@gmail.com [Post Graduate Department of Physics, Sanathana Dharma College, Alappuzha, Kerala (India); Raveendran, R. [Nanoscience Research Laboratory, Sree Narayana College, Kollam, Kerala 691001 (India)

    2014-10-15

    The fast development in nanotechnology makes enthusiastic interest in developing nanomaterials having tailor made properties. Cerium mixed oxide materials have received great attention due to their UV absorption property, high reactivity, stability at high temperature, good electrical property etc and these materials find wide applications in solid oxide fuel cells, solar control films, cosmetics, display units, gas sensors etc. In this study cerium mixed oxide compounds were prepared by co-precipitation method. All the samples were doped with Zn (II) and Fe (II). Preliminary characterizations such as XRD, SEM / EDS, TEM were done. UV - Vis, Diffuse reflectance, PL, FT-IR, Raman and ac conductivity studies of the samples were performed.

  2. Electrical, thermal and infrared studies of cerium(III) orthovanadate

    International Nuclear Information System (INIS)

    Cerium(III) orthovandate with a small deviation from stoichiometric composition is a p-type semiconductor between 30 and 800 degC. The electrical conduction in cerium(III) orthovanadate is due to thermally activated hopping of holes on equivalent Ce3+ -Ce4+ lattice sites. The DTA result of CeVO4 indicated a possible phase transition at about 70 degC. The IR spectrum of the sample showed bands at 865 and 810 cm-1, typical of VO4 group of orthovanadates. (author). 10 refs., 3 figs

  3. Plasmonic hydrogen sensing with nanostructured metal hydrides.

    Science.gov (United States)

    Wadell, Carl; Syrenova, Svetlana; Langhammer, Christoph

    2014-12-23

    In this review, we discuss the evolution of localized surface plasmon resonance and surface plasmon resonance hydrogen sensors based on nanostructured metal hydrides, which has accelerated significantly during the past 5 years. We put particular focus on how, conceptually, plasmonic resonances can be used to study metal-hydrogen interactions at the nanoscale, both at the ensemble and at the single-nanoparticle level. Such efforts are motivated by a fundamental interest in understanding the role of nanosizing on metal hydride formation processes in the quest to develop efficient solid-state hydrogen storage materials with fast response times, reasonable thermodynamics, and acceptable long-term stability. Therefore, a brief introduction to the thermodynamics of metal hydride formation is also given. However, plasmonic hydrogen sensors not only are of academic interest as research tool in materials science but also are predicted to find more practical use as all-optical gas detectors in industrial and medical applications, as well as in a future hydrogen economy, where hydrogen is used as a carbon free energy carrier. Therefore, the wide range of different plasmonic hydrogen sensor designs already available is reviewed together with theoretical efforts to understand their fundamentals and optimize their performance in terms of sensitivity. In this context, we also highlight important challenges to be addressed in the future to take plasmonic hydrogen sensors from the laboratory to real applications in devices, including poisoning/deactivation of the active materials, sensor lifetime, and cross-sensitivity toward other gas species. PMID:25427244

  4. Stepwise hydrochloric acid extraction of monazite hydroxides for the recovery of cerium lean rare earths, cerium, uranium and thorium

    International Nuclear Information System (INIS)

    Monazite sand is normally processed by the caustic soda route to produce mixed rare earth chloride, thorium hydroxide and trisodium phosphate. Bulk of the mixed rare earth chloride is used for the preparation of FC catalysts. Recently some of the catalyst producers have shown preference to cerium depleted (lanthanum enriched) rare earth chloride rather than the natural rare earth chloride obtained from monazite. Therefore, a process for producing cerium depleted rare earth chloride, cerium, thorium and uranium from rare earth + thorium hydroxide obtained by treating monazite, based on stepwise hydrochloric acid extraction, was developed in the authors laboratory. The process involves drying of the mixed rare earth-thorium hydroxide cake obtained by monazite-caustic soda process followed by stepwise extraction of the dried cake with hydrochloric acid under specified conditions

  5. METHOD AND APPARATUS FOR MAKING URANIUM-HYDRIDE COMPACTS

    Science.gov (United States)

    Wellborn, W.; Armstrong, J.R.

    1959-03-10

    A method and apparatus are presented for making compacts of pyrophoric hydrides in a continuous operation out of contact with air. It is particularly useful for the preparation of a canned compact of uranium hydride possessing high density and purity. The metallic uranium is enclosed in a container, positioned in a die body evacuated and nvert the uranium to the hydride is admitted and the container sealed. Heat is applied to bring about the formation of the hydride, following which compression is used to form the compact sealed in a container ready for use.

  6. Spectrophotometric determination of volautile inorganic hydrides in binary gaseous mixtures

    International Nuclear Information System (INIS)

    A study was made on possibility of single and continuons analysis of binary mixtures (hydride-gas) for the content of volatile inorganic hydrides (VIH) from absorption spectra in the 185-280 nm band. Dependences of the percentage of VIH transmission on the wavelength are presented. It is shown that the maximum of their absorption depends on the element-hydrogen the bond length and binding energy. Detection limit for boron hydride was established to be n x 10-3% vol at 185-190 nm wavelength. Technique for spectrophotometric hydride determination in binary mixtures with hydrogen, argon, helium was developed. The technique provides the continuous control of gaseous mixture composition

  7. Identification of the zirconium hydrides metallography in zircaloy-2

    International Nuclear Information System (INIS)

    Technique for the Identification of the zirconium hydrides in metallographic specimens have been developed. Microhardness, quantitative estimation and relative orientation of the present hydrides as well as grain size determination of the different Zircaloy-2 tube specimens have also been made. The specimens used were corrosion- tested in water during various periods of time at 300 degree castrating, prior to the metallographic examination. Reference specimens, as received, and heavily hydride specimens in a hydrogen atmosphere at 800 degree centigrees, have been used in the previous stages of the work. No difficulties have been met in this early stage of acquaintanceship with the zirconium hydrides. (Author) 5 refs

  8. Properties of Cerium Containing Lead Free Solder

    Science.gov (United States)

    Xie, Huxiao

    With increasing concerns of the intrinsic toxicity of lead (Pb) in electronics, a series of tin (Sn) based alloys involving silver (Ag) and copper (Cu) have been proposed as replacements for Pb-Sn solder and widely accepted by industry. However, they have a higher melting point and often exhibit poorer damage tolerance than Pb-Sn alloys. Recently, a new class of alloys with trace amount of rare-earth (RE) elements has been discovered and investigated. In previous work from Prof. Chawla's group, it has been shown that cerium (Ce)-based Pb-free solder are less prone to oxidation and Sn whiskering, and exhibit desirable attributes of microstructural refinement and enhanced ductility relative to lanthanum (La)-based Sn-3.9Ag-0.7Cu (SAC) alloy. Although the formation of RESn3 was believed to be directly responsible for the enhanced ductility in RE-containing SAC solder by allowing microscopic voids to nucleate throughout the solder volume, this cavitation-based mechanism needs to be validated experimentally and numerically. Additionally, since the previous study has exhibited the realistic feasibility of Ce-based SAC lead-free solder alloy as a replacement to conventional SAC alloys, in this study, the proposed objective focuses on the in in-depth understanding of mechanism of enhanced ductility in Ce-based SAC alloy and possible issues associated with integration of this new class of solder into electronic industry, including: (a) study of long-term thermal and mechanical stability on industrial metallization, (b) examine the role of solder volume and wetting behavior of the new solder, relative to Sn-3.9Ag-0.7Cu alloys, (c) conduct experiments of new solder alloys in the form of mechanical shock and electromigration. The research of this new class alloys will be conducted in industrially relevant conditions, and the results would serve as the first step toward integration of these new, next generation solders into the industry.

  9. Modulated structures in oxidized cerium niobates

    International Nuclear Information System (INIS)

    Three previously reported oxidized cerium niobate phases CeNbO4+x (x = 0.08, 0.25, and 0.33) have been synthesized and characterized by X-ray powder and electron diffraction. All three phases display structures which are modulated variants of a parent fergusonite-type CeIIINbO4 structure (I2/a, a = 5.5342(2) angstrom, b = 11.4016(6) angstrom, c = 5.1583(3) angstrom, β = 94.600(5)degree). The x = 0.08 phase with parent unit cell (I2/a, a = 5.3029(8) angstrom, b = 11.483(2) angstrom, c = 5.2515(8) angstrom, β = 91.32(2)degree) is a two-dimensional, incommensurately modulated phase characterized by incommensurate primary modulation wavevectors q1 ∼ [0.345, 0, 0.138]p* and q2 ∼ [-0.069, 0, 0.172]p* (p for parent). The x = 0.25 phase with parent unit cell (I2/a, a = 5.3522(8) angstrom, b = 11.374(3) angstrom, c = 5.116(1) angstrom, β = 93.34(2)degree) is a commensurately modulated superstructure phase characterized by the reciprocal space unit cell ar* = 1/12[402]p*, br* = 1/4[020]p*, and cr* = 1/3[101]p* (r for resultant). The x = 0.33 phase with parent unit cell (I1, a = 5.4374(8) angstrom, b = 11.189(2) angstrom, c = 5.1458(8) angstrom, α = 90.56(1), β = 94.37(1), γ = 88.19(1)degree) is again commensurately modulated with q = 1/3[101]p*. The close structural relationship between the three oxidized phases and possible interstitial oxygen sites in the CeIIINbO4 structure are discussed

  10. Cerium Oxyhydroxide Clusters: Formation, Structure and Reactivity

    Energy Technology Data Exchange (ETDEWEB)

    Frederic Aubriet; Jean-Jacques Gaumet; Wibe A de Jong; Groenewold, Gary S (058000); Gianotto, Anita K (057404); McIlwain, Michael E (051783); Michael J. Van Stipdonk; Christopher M. Leavitt

    2009-06-01

    Cerium oxyhydroxide cluster anions were produced by irradiating ceric oxide particles using 355 nm laser pulses that were synchronized with pulses of nitrogen gas admitted to the irradiation chamber. The gas pulse stabilized the nascent clusters that are largely anhydrous [CexOy] ions and neutrals. These initially-formed species react with water, principally forming closed-shell (c-s) oxohydroxy species that are described by the general formula [CexOy(OH)z]-. In general, the extent of hydroxylation varies from a value of 3 OH per Ce atom when x = 1 to a value slightly greater than 1 for x > 8. The Ce3 and Ce6 species deviate significantly from this trend: the x = 3 cluster accommodates more hydroxyl moieties compared to neighboring congeners at x = 2 and x = 4. Conversely, the x = 6 cluster is significantly less hydroxylated. Density functional theory (DFT) modeling of the cluster structures show that the hydrated clusters are hydrolyzed, and contain one-to-multiple hydroxide moieties, but not datively bound water. DFT also predicts an energetic preference for formation of highly symmetric structures as the size of the clusters increases. The calculated structures indicate that the ability of the Ce3 oxyhydroxide to accommodate more extensive hydroxylation is due to a more open, hexagonal structure in which the Ce atoms can participate in multiple hydrolysis reactions. Conversely the Ce6 oxyhydroxide has an octahedral structure that is not conducive to hydrolysis. In addition to the c-s clusters, open-shell (o-s) oxyhydroxides and superoxides are also formed, and they become more prominent as the size of the clusters increases, suggesting that the larger ceria clusters have an increased ability to stabilize a non-bonding electron. The overall intensity of the clusters tends to monotonically decrease as the cluster size increases, however this trend is interrupted at Ce13, which is significantly more stable compared to neighboring congeners, suggesting formation of

  11. Cerium Oxyhydroxide Clusters: Formation, Structure and Reactivity

    Energy Technology Data Exchange (ETDEWEB)

    Aubriet, F.; Gaumet, Jean-Jacques; De Jong, Wibe A.; Groenewold, G. S.; Gianotto, Anita K.; McIIwain, Michael E.; Van Stipdonk, Michael J.; Leavitt, Christopher M.

    2009-05-11

    Cerium oxyhydroxide cluster anions were produced by irradiating ceric oxide particles using 355 nm laser pulses that were synchronized with pulses of nitrogen gas admitted to the irradiation chamber. The gas pulse stabilized the nascent clusters that are largely anhydrous [CexOy] ions and neutrals. These initially-formed species react with water, principally forming closed-shell (c-s) oxohydroxy species that are described by the general formula [CexOy(OH)z]-. In general, the extent of hydroxylation varies from a value of 3 OH per Ce atom when x = 1 to a value slightly greater than 1 for x > 8. The Ce3 and Ce6 species deviate significantly from this trend: the x = 3 cluster accommodates more hydroxyl moieties compared to neighboring congeners at x = 2 and x = 4. Conversely, the x = 6 cluster is significantly less hydroxylated. Density functional theory (DFT) modeling of the cluster structures show that the hydrated clusters are hydrolyzed, and contain one-to-multiple hydroxide moieties, but not datively bound water. DFT also predicts an energetic preference for formation of highly symmetric structures as the size of the clusters increases. The calculated structures indicate that the ability of the Ce3 oxyhydroxide to accommodate more extensive hydroxylation is due to a more open, hexagonal structure in which the Ce atoms can participate in multiple hydrolysis reactions. Conversely the Ce6 oxyhydroxide has an octahedral structure that is not conducive to hydrolysis. In addition to the c-s clusters, open-shell (o-s) oxyhydroxides and superoxides are also formed, and they become more prominent as the size of the clusters increases, suggesting that the larger ceria clusters have an increased ability to stabilize a non-bonding electron. The overall intensity of the clusters tends to monotonically decrease as the cluster size increases, however this trend is interrupted at Ce13, which is significantly more stable compared to neighboring congeners, suggesting formation of

  12. Cerium tartrate as a corrosion inhibitor for AA 2024-T3

    International Nuclear Information System (INIS)

    Highlights: • Cerium tartrate was found to be an effective inhibitor for AA 2024-T3. • Both anodic and cathodic inhibitions were present during the corrosion process. • The corrosion of Al2CuMg phase was well inhibited by cerium tartrate. - Abstract: A new corrosion inhibitor, cerium tartrate, was synthetized. The inhibition behavior of cerium tartrate for 2024-T3 aluminum alloy was investigated in 0.05 M NaCl solution. The immersion tests indicate that the corrosion of Al2CuMg phase was well inhibited. The electrochemical results show that both anodic and cathodic inhibitions are present during the corrosion process. The surface characterizations reveal that the protective film of cerium tartrate inhibits the dealloying of Al2CuMg phase in the initial stage, and then cerium ions transform to cerium oxide/hydroxides and appear at the Al2CuMg phase, blocking the further corrosion at those corrosion sites

  13. Nanoparticulate cerium dioxide and cerium dioxide-titanium dioxide composite thin films on glass by aerosol assisted chemical vapour deposition

    International Nuclear Information System (INIS)

    Two series of composite thin films were deposited on glass by aerosol assisted chemical vapour deposition (AACVD)-nanoparticulate cerium dioxide and nanoparticulate cerium dioxide embedded in a titanium dioxide matrix. The films were analysed by a range of techniques including UV-visible absorption spectroscopy, X-ray diffraction, scanning electron microscopy and energy dispersive analysis by X-rays. The AACVD prepared films showed the functional properties of photocatalysis and super-hydrophilicity. The CeO2 nanoparticle thin films displaying photocatalysis and photo-induced hydrophilicity almost comparable to that of anatase titania.

  14. Uranium-zirconium hydride fuel properties

    Energy Technology Data Exchange (ETDEWEB)

    Olander, D. [Department of Nuclear Engineering, University of California at Berkeley, Berkeley, CA 94720 (United States)], E-mail: fuelpr@nuc.berkeley.edu; Greenspan, Ehud [Department of Nuclear Engineering, University of California at Berkeley, Berkeley, CA 94720 (United States); Garkisch, Hans D. [Westinghouse Electric Company LLC, Pittsburgh, PA 15236 (United States); Petrovic, Bojan [School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA (United States)

    2009-08-15

    Properties of the two-phase hydride U{sub 0.3}ZrH{sub 1.6} pertinent to performance as a nuclear fuel for LWRs are reviewed. Much of the available data come from the Space Nuclear Auxiliary Power (SNAP) program of 4 decades ago and from the more restricted data base prepared for the TRIGA research reactors some 3 decades back. Transport, mechanical, thermal and chemical properties are summarized. A principal difference between oxide and hydride fuels is the high thermal conductivity of the latter. This feature greatly decreases the temperature drop over the fuel during operation, thereby reducing the release of fission gases to the fraction due only to recoil. However, very unusual early swelling due to void formation around the uranium particles has been observed in hydride fuels. Avoidance of this source of swelling limits the maximum fuel temperature to {approx}650 deg. C (the design limit recommended by the fuel developer is 750 deg. C). To satisfy this temperature limitation, the fuel-cladding gap needs to be bonded with a liquid metal instead of helium. Because the former has a thermal conductivity {approx}100 times larger than the latter, there is no restriction on gap thickness as there is in helium-bonded fuel rods. This opens the possibility of initial gap sizes large enough to significantly delay the onset of pellet-cladding mechanical interaction (PCMI). The large fission-product swelling rate of hydride fuel (3x that of oxide fuel) requires an initial radial fuel-cladding gap of {approx}300 m if PCMI is to be avoided. The liquid-metal bond permits operation of the fuel at current LWR linear-heat-generation rates without exceeding any design constraint. The behavior of hydrogen in the fuel is the source of phenomena during operation that are absent in oxide fuels. Because of the large heat of transport (thermal diffusivity) of H in ZrH{sub x}, redistribution of hydrogen in the temperature gradient in the fuel pellet changes the initial H/Zr ratio of 1

  15. Uranium-zirconium hydride fuel properties

    International Nuclear Information System (INIS)

    Properties of the two-phase hydride U0.3ZrH1.6 pertinent to performance as a nuclear fuel for LWRs are reviewed. Much of the available data come from the Space Nuclear Auxiliary Power (SNAP) program of 4 decades ago and from the more restricted data base prepared for the TRIGA research reactors some 3 decades back. Transport, mechanical, thermal and chemical properties are summarized. A principal difference between oxide and hydride fuels is the high thermal conductivity of the latter. This feature greatly decreases the temperature drop over the fuel during operation, thereby reducing the release of fission gases to the fraction due only to recoil. However, very unusual early swelling due to void formation around the uranium particles has been observed in hydride fuels. Avoidance of this source of swelling limits the maximum fuel temperature to ∼650 deg. C (the design limit recommended by the fuel developer is 750 deg. C). To satisfy this temperature limitation, the fuel-cladding gap needs to be bonded with a liquid metal instead of helium. Because the former has a thermal conductivity ∼100 times larger than the latter, there is no restriction on gap thickness as there is in helium-bonded fuel rods. This opens the possibility of initial gap sizes large enough to significantly delay the onset of pellet-cladding mechanical interaction (PCMI). The large fission-product swelling rate of hydride fuel (3x that of oxide fuel) requires an initial radial fuel-cladding gap of ∼300 m if PCMI is to be avoided. The liquid-metal bond permits operation of the fuel at current LWR linear-heat-generation rates without exceeding any design constraint. The behavior of hydrogen in the fuel is the source of phenomena during operation that are absent in oxide fuels. Because of the large heat of transport (thermal diffusivity) of H in ZrHx, redistribution of hydrogen in the temperature gradient in the fuel pellet changes the initial H/Zr ratio of 1.6 to ∼1.45 at the center and

  16. Cathodic electrodeposition of cerium-based oxides on carbon steel from concentrated cerium nitrate solutions

    Energy Technology Data Exchange (ETDEWEB)

    Hamlaoui, Y. [Laboratoire d' Etudes des Materiaux en Milieux Agressifs (LEMMA), Pole Sciences et Technologie, Universite de La Rochelle, Avenue Michel Crepeau, 17042 La Rochelle Cedex 1 (France); Pedraza, F. [Laboratoire d' Etudes des Materiaux en Milieux Agressifs (LEMMA), Pole Sciences et Technologie, Universite de La Rochelle, Avenue Michel Crepeau, 17042 La Rochelle Cedex 1 (France)], E-mail: fpedraza@univ-lr.fr; Remazeilles, C.; Cohendoz, S.; Rebere, C. [Laboratoire d' Etudes des Materiaux en Milieux Agressifs (LEMMA), Pole Sciences et Technologie, Universite de La Rochelle, Avenue Michel Crepeau, 17042 La Rochelle Cedex 1 (France); Tifouti, L. [Laboratoire de Genie de l' Environnement, Universite Badji Mokhtar, BP 1223, 23020 El Hadjar-Annaba (Algeria); Creus, J. [Laboratoire d' Etudes des Materiaux en Milieux Agressifs (LEMMA), Pole Sciences et Technologie, Universite de La Rochelle, Avenue Michel Crepeau, 17042 La Rochelle Cedex 1 (France)

    2009-02-15

    In this work the elaboration by cathodic electrodeposition of cerium-based oxides on carbon steel from relatively concentrated cerium nitrate solutions is investigated. In particular, the study presented here (Part I) focuses on the electrochemical and analytical characterisation of the films and on the correlations between the electrochemical features and the characteristics of the layers. The effect of other parameters such as concentration, temperature, pH and additives to improve the behaviour of the film against corrosion will be investigated in part II of the study. The electrochemical characterisation will reveal that Ce(IV)-steel interactions can be responsible for some weak electrochemical waves appearing in the cyclic voltammograms that often are attributed to oxygen or nitrates reduction. This results from the oxidation of Ce(III) solutions to Ce(IV) in contact with air. Furthermore, the deposits strongly depend on the applied current density. Low current densities do not render fully covering deposits on the steel and a carbonated green rust will appear. On the contrary, the increase of the current density leads to denser layers of relatively small crystallite size that readily covers the steel surface. The deposits have a needle-like morphology and the Ce content achieves a plateau of about 20-22 at.%. However, a significant network of cracks appears probably occurring during the deposition process itself. The differential scanning calorimetry (DSC) results indicate that the deposits are not fully crystalline after 550 deg. C in contrast with the X-ray diffraction (XRD) patterns that unambiguously show a fluorite-type CeO{sub 2} phase whose crystallite size decreases with increasing the current density. The rinsing medium also brings about different features of the films. Rinsing with water allows to incorporate more nitrates and to adsorb CO{sub 2} than when rinsing with ethanol. However, R-OH bonds will be trapped in the latter.

  17. Cathodic electrodeposition of cerium-based oxides on carbon steel from concentrated cerium nitrate solutions

    International Nuclear Information System (INIS)

    In this work the elaboration by cathodic electrodeposition of cerium-based oxides on carbon steel from relatively concentrated cerium nitrate solutions is investigated. In particular, the study presented here (Part I) focuses on the electrochemical and analytical characterisation of the films and on the correlations between the electrochemical features and the characteristics of the layers. The effect of other parameters such as concentration, temperature, pH and additives to improve the behaviour of the film against corrosion will be investigated in part II of the study. The electrochemical characterisation will reveal that Ce(IV)-steel interactions can be responsible for some weak electrochemical waves appearing in the cyclic voltammograms that often are attributed to oxygen or nitrates reduction. This results from the oxidation of Ce(III) solutions to Ce(IV) in contact with air. Furthermore, the deposits strongly depend on the applied current density. Low current densities do not render fully covering deposits on the steel and a carbonated green rust will appear. On the contrary, the increase of the current density leads to denser layers of relatively small crystallite size that readily covers the steel surface. The deposits have a needle-like morphology and the Ce content achieves a plateau of about 20-22 at.%. However, a significant network of cracks appears probably occurring during the deposition process itself. The differential scanning calorimetry (DSC) results indicate that the deposits are not fully crystalline after 550 deg. C in contrast with the X-ray diffraction (XRD) patterns that unambiguously show a fluorite-type CeO2 phase whose crystallite size decreases with increasing the current density. The rinsing medium also brings about different features of the films. Rinsing with water allows to incorporate more nitrates and to adsorb CO2 than when rinsing with ethanol. However, R-OH bonds will be trapped in the latter

  18. Stress field computation for hydride blister forming in Zr alloys

    International Nuclear Information System (INIS)

    Hydrogen migration under thermal gradient in zirconium alloys results in formation of hydride blisters. An array of blisters makes Zirconium alloy components of nuclear reactors susceptible to fracture. The whole process of hydride blister formation and fracture of these components is very complex and involves hydrogen migration under thermal gradient, hydride precipitation, straining of the matrix, setting up of hydrostatic stress gradient, enhanced hydrogen migration under the combined influence of thermal and stress gradients, stress reorientation of hydrides, cracking of hydrides, crack growth by delayed hydride cracking mechanism, interlinking of blisters and spontaneous fracture of the component. In this work we estimate the stress components in hydride blisters and the surrounding matrix for certain assumed blister depth as a function of hydride matrix yield strength ratio. The simulation was carried out for a semi ellipsoidal blister using ABAQUS finite element package. The blister formation was simulated by single step and multiple step transformation of the matrix to hydride. It is felt that the same methodology can be used to estimate the stress field around semi constrained inclusion such as hydride blister(s) in hydride forming metals like uranium, zirconium, titanium etc. and of localized corrosion products in metals and alloys. A matrix of dimension in the ratio 5 (along direction 1):1 (along direction 2) was considered for the computations. The Zr matrix having hexagonal crystal structure and faced centered cubic zirconium hydride was modeled as elastically isotropic. Both matrix and hydride was modeled to undergo linear work hardening up to ultimate tensile strength (=1.25Xyield strength), corresponding to a plastic strain of 10 percent. A small strain small displacement theory was adopted. Computations were made for an axisymmetric case with the symmetry axis along the 2 direction. Transformation of zirconium hydrogen solid solution into hydride

  19. Electrorheological Effects of Cerium-Doped TiO2

    Institute of Scientific and Technical Information of China (English)

    尹剑波; 赵晓鹏

    2001-01-01

    It is found that the doping of cerium ion into anatase TiO2 can improve the electrorheological (ER) effects of TiO2 and broaden the operational temperature range. Especially, the substitution of 7-11 mol% of the cerium dopant for Ti can obtain a relatively high shear stress, t-7.4kPa (at 4kV/mm), which is ten times larger than that of pure TiO2 ER fluid. Also, the typical Ce-doped TiO2 ER fluid shows the highest shear stress at 80℃, but 40℃ for pure TiO2 ER fluid. The dielectric loss and dielectric constant at a low frequency of TiO2 is improved by the doping of cerium, and the temperature dependence of the dielectric properties shows an obvious differnce between pure and doped TiO2 ER fluids. These can well explain the ER behaviour of doped TiO2. Furthermore, the change of rheological and dielectric properties is discussed on the basis of the lattice distortion and defects in TiO2 arising from the doping of cerium.

  20. Purification of cerium, neodymium and gadolinium for low background experiments

    Directory of Open Access Journals (Sweden)

    Boiko R.S.

    2014-01-01

    Full Text Available Cerium, neodymium and gadolinium contain double beta active isotopes. The most interesting are 150Nd and 160Gd (promising for 0ν2β search, 136Ce (2β+ candidate with one of the highest Q2β. The main problem of compounds containing lanthanide elements is their high radioactive contamination by uranium, radium, actinium and thorium. The new generation 2β experiments require development of methods for a deep purification of lanthanides from the radioactive elements. A combination of physical and chemical methods was applied to purify cerium, neodymium and gadolinium. Liquid-liquid extraction technique was used to remove traces of Th and U from neodymium, gadolinium and for purification of cerium from Th, U, Ra and K. Co-precipitation and recrystallization methods were utilized for further reduction of the impurities. The radioactive contamination of the samples before and after the purification was tested by using ultra-low-background HPGe gamma spectrometry. As a result of the purification procedure the radioactive contamination of gadolinium oxide (a similar purification efficiency was reached also with cerium and neodymium oxides was decreased from 0.12 Bq/kg to 0.007 Bq/kg in 228Th, from 0.04 Bq/kg to <0.006 Bq/kg in 226Ra, and from 0.9 Bq/kg to 0.04 Bq/kg in 40K. The purification methods are much less efficient for chemically very similar radioactive elements like actinium, lanthanum and lutetium.

  1. Enhanced K-edge angiography utilizing cerium-target diode

    International Nuclear Information System (INIS)

    The cerium-target x-ray tube is useful in order to perform cone-beam K-edge angiography because Kα rays from the cerium target are absorbed effectively by iodine-based contrast mediums. The x-ray generator consists of a main controller, an x-ray tube unit with a high-voltage circuit and an insulation transformer, and a personal computer. The tube is a glass-enclosed diode with a cerium target and a 0.5-mm-thick beryllium window. The maximum tube voltage and current were 65 kV and 0.4 mA, respectively, and the focal-spot sizes were approximately 1 x 1 mm. Sharp cerium Kα lines were left using a barium sulfate filter, and the x-ray intensity was 16.8 μGy/s at 1.0 m from the source with a tube voltage of 60 kV and a current of 0.40 mA. Angiography was performed with an x-ray film (Fuji IX 100) using iodine-based microspheres 15 μm in diameter. In angiography of non-living animals, we observed fine blood vessels of 100 μm or less with high contrasts. (author)

  2. Electrodeposition of cerium from aqueous cerous chloride solutions

    International Nuclear Information System (INIS)

    Cerium was plated as a grey, metallic, adherent deposit from aqueous cerous chloride baths containing certain organic addition agents. The cathodic current efficiency was determined for each case. Chemical analysis indicates that the purity of the metal is better than 99.0 per cent. (author). 7 refs

  3. 40 CFR 721.8657 - Cerium, hydroxy oleate propionate complexes.

    Science.gov (United States)

    2010-07-01

    ... complexes. 721.8657 Section 721.8657 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.8657 Cerium, hydroxy oleate propionate complexes. (a) Chemical substance..., hydroxy oleate propionate complexes (PMN P-99-0026) is subject to reporting under this section for...

  4. Thermoluminescence studies in cerium doped NaCl crystals

    International Nuclear Information System (INIS)

    Cerium is known to enter substitutionally in trivalent state when doped in alkali halides. Cerium doped NaCl crystals exhibit greatly enhanced thermoluminescence output upon X-irradiation at RT, the intensity of emission being about 10 times that in undoped crystals for similar dosage of irradiation. The cerium doped crystals give upon X-irradiation a very intense glow peak at 145degC with shoulders at 120degC and 210degC. Upon partially bleaching the crystal with F-light, the peak at 120degC becomes prominent probably due to faster bleaching of the glow at 145degC. From further optical bleaching studies, it is concluded that the glow peak at around 120degC is due to cerium centres in the irradiated crystal and the 145degC peak due to F centres. This F centre emission occurs at lower temperature, compared to that in the undoped crystals where it occurs at around 180degC. The spectral emission in the Ce doped crystals is in the blue-green region as compared to the emission in the blue region in undoped crystals. The trap depth and other parameters of the 120degC glow peak are estimated by the total curve fitting method. (author)

  5. Competition between magnetic order and Kondo effect in cerium compounds

    International Nuclear Information System (INIS)

    We present a mean-field analysis of the competition between magnetic order and Kondo effect in a Kondo-lattice model usually employed to discuss properties of certain cerium compounds. A phase diagram is obtained showing an antiferromagnetic phase and a Kondo-compensated regime, in agreement with the Doniach diagram. A general discussion of the mean-field approach is also presented

  6. Electrical measurements in the cerium oxide doped samples

    International Nuclear Information System (INIS)

    Electrical behaviour of an interface formed by cerium oxide doped system has been studied. The system was (Ce O2)1-0,005 (Y O 1,5)0,005/(Ce O2)1-0,14(Y O 1,5)0,14. This work relates results of impedance analysis, and curves U(I) at different temperatures and polarizations conditions. (author)

  7. Purification of cerium, neodymium and gadolinium for low background experiments

    Science.gov (United States)

    Boiko, R. S.; Barabash, A. S.; Belli, P.; Bernabei, R.; Cappella, F.; Cerulli, R.; Danevich, F. A.; Incicchitti, A.; Laubenstein, M.; Mokina, V. M.; Nisi, S.; Poda, D. V.; Polischuk, O. G.; Tretyak, V. I.

    2014-01-01

    Cerium, neodymium and gadolinium contain double beta active isotopes. The most interesting are 150Nd and 160Gd (promising for 0ν2β search), 136Ce (2β+ candidate with one of the highest Q2β). The main problem of compounds containing lanthanide elements is their high radioactive contamination by uranium, radium, actinium and thorium. The new generation 2β experiments require development of methods for a deep purification of lanthanides from the radioactive elements. A combination of physical and chemical methods was applied to purify cerium, neodymium and gadolinium. Liquid-liquid extraction technique was used to remove traces of Th and U from neodymium, gadolinium and for purification of cerium from Th, U, Ra and K. Co-precipitation and recrystallization methods were utilized for further reduction of the impurities. The radioactive contamination of the samples before and after the purification was tested by using ultra-low-background HPGe gamma spectrometry. As a result of the purification procedure the radioactive contamination of gadolinium oxide (a similar purification efficiency was reached also with cerium and neodymium oxides) was decreased from 0.12 Bq/kg to 0.007 Bq/kg in 228Th, from 0.04 Bq/kg to <0.006 Bq/kg in 226Ra, and from 0.9 Bq/kg to 0.04 Bq/kg in 40K. The purification methods are much less efficient for chemically very similar radioactive elements like actinium, lanthanum and lutetium.

  8. High ramp rate thermogravimetric analysis of zirconium(II) hydride and titanium(II) hydride

    International Nuclear Information System (INIS)

    Highlights: • A unique arc image device has been proposed for high ramp rate thermogravimetry. • Powder oxidation influences decomposition kinetics at temperatures below 933 K. • Particle size has a negligible effect on TiH2 decomposition behavior. • Improvements to the device are required to conduct accurate kinetic analysis. - Abstract: Zirconium and titanium hydride are utilized in liquid phase metal foam processing techniques. This application results in immediate exposure to molten metal and almost immediate decomposition at high temperatures. Most decomposition characterization techniques utilize slow heating rates and are unable to capture the decomposition behavior of hydrides under foam processing conditions. In order to address this issue a specialized high ramp rate thermogravimetric analyzer was created from a xenon arc image refiner. In addition to thermogravimetry, complimentary techniques including X-ray diffraction and scanning electron microscopy were used to characterize hydride decomposition and compare the results to literature. Hydrides were partially oxidized and separated into particles size ranges to evaluate the influence of these factors on decomposition. Oxidizing treatments were found to decrease decomposition rate only at temperatures below 933 K (660 °C) while particle size effects appeared to be negligible. Several improvements to the unique TGA apparatus presented in the current work are suggested to allow reliable kinetic modeling and analysis

  9. Cerium as a surrogate in the plutonium immobilization waste form

    Science.gov (United States)

    Marra, James Christopher

    In the aftermath of the Cold War, approximately 50 tonnes (MT) of weapons useable plutonium (Pu) has been identified as excess. The U.S. Department of Energy (DOE) has decided that at least a portion of this material will be immobilized in a titanate-based ceramic for final disposal in a geologic repository. The baseline formulation was designed to produce a ceramic consisting primarily of a highly substituted pyrochlore with minor amounts of brannerite and hafnia-substituted rutile. Since development studies with actual actinide materials is difficult, surrogates have been used to facilitate testing. Cerium has routinely been used as an actinide surrogate in actinide chemistry and processing studies. Although cerium appeared as an adequate physical surrogate for powder handling and general processing studies, cerium was found to act significantly different from a chemical perspective in the Pu ceramic form. The reduction of cerium at elevated temperatures caused different reaction paths toward densification of the respective forms resulting in different phase assemblages and microstructural features. Single-phase fabrication studies and cerium oxidation state analyses were performed to further quantify these behavioral differences. These studies indicated that the major phases in the final phase assemblages contained point defects likely leading to their stability. Additionally, thermochemical arguments predicted that the predominant pyrochlore phase in the ceramic was metastable. The apparent metastabilty associated with primary phase in the Pu ceramic form indicated that additional studies must be performed to evaluate the thermodynamic properties of these compounds. Moreover, the metastability of this predominant phase must be considered in assessment of long-term behavior (e.g. radiation stability) of this ceramic.

  10. Preparation, Characterization and Antibacterial Property of Cerium Substituted Hydroxyapatite Nanoparticles

    Institute of Scientific and Technical Information of China (English)

    Lin Yingguang; Yang Zhuoru; Cheng Jiang

    2007-01-01

    Nanoparticles of hydroxyapatite (HAP) and cerium substituted hydroxyapatite (CeHAP) with the atomic ratio of Ce/[Ca+Ce] (xCe) from 0 to 0.2 were prepared by sol-gel-supercritical fluid drying (SCFD) method. The nanoparticles were characterized by TEM, XRD, and FT-IR, and the effects of cerium on crystal structure, crystallinity, and particle shape were discussed. With the tests of bacterial inhibition zone and antibacterial ratio, the antibacterial property of HAP and CeHAP nanoparticles on Escherichia coli, Staphylococcus aureus, Lactobacillus were researched. Results showed that the nanoparticles of HAP and CeHAP could be made by sol-gel-SCFD, cerium could partially substitute for calcium and enter the structure of HAP. After substitution, the crystallinity, the IR wavenumbers of bonds in CeHAP decreased gradually with increase of cerium substitution, and the morphology of the nanoparticles changed from the short rod-shaped HAP to the needle-shaped CeHAP. The nanoparticles of HAP and CeHAP with xCe below 0.08 had antibacterial property only forcibly contacting with the test bacteria at the test concentration of 0.1 g·ml-1, however, the CeHAP nanoparticles had antibacterial ability at that concentration no matter statically or dynamically contacting with the test bacteria when xCe was above 0.08, and the antibacterial ability gets better with the increase of xCe, indicating that the antibacterial property was improved after calcium was partially substituted by cerium. The improved antibacterial effects of CeHAP nanoparticle on Lactobacillus showed its potential ability to anticaries.

  11. Electrochemical and Optical Properties of Magnesium-Alloy Hydrides Reviewed

    Directory of Open Access Journals (Sweden)

    Thirugnasambandam G. Manivasagam

    2012-10-01

    Full Text Available As potential hydrogen storage media, magnesium based hydrides have been systematically studied in order to improve reversibility, storage capacity, kinetics and thermodynamics. The present article deals with the electrochemical and optical properties of Mg alloy hydrides. Electrochemical hydrogenation, compared to conventional gas phase hydrogen loading, provides precise control with only moderate reaction conditions. Interestingly, the alloy composition determines the crystallographic nature of the metal-hydride: a structural change is induced from rutile to fluorite at 80 at.% of Mg in Mg-TM alloy, with ensuing improved hydrogen mobility and storage capacity. So far, 6 wt.% (equivalent to 1600 mAh/g of reversibly stored hydrogen in MgyTM(1-yHx (TM: Sc, Ti has been reported. Thin film forms of these metal-hydrides reveal interesting electrochromic properties as a function of hydrogen content. Optical switching occurs during (dehydrogenation between the reflective metal and the transparent metal hydride states. The chronological sequence of the optical improvements in optically active metal hydrides starts with the rare earth systems (YHx, followed by Mg rare earth alloy hydrides (MgyGd(1-yHx and concludes with Mg transition metal hydrides (MgyTM(1-yHx. In-situ optical characterization of gradient thin films during (dehydrogenation, denoted as hydrogenography, enables the monitoring of alloy composition gradients simultaneously.

  12. Kinetics of Final Degassing of Hydrogen Desorption by Metal Hydrides

    CERN Document Server

    Drozdov, I V

    2014-01-01

    The proposed model concerns the 'confluent shrinking core' scenario and reproduces the desorption kinetic after the complete decay of the stoichiometric hydride ($\\beta$-phase). The exact analytical solution is obtained, the numerical values are demonstrated by the example of magnesium hydride.

  13. High energy density battery based on complex hydrides

    Science.gov (United States)

    Zidan, Ragaiy

    2016-04-26

    A battery and process of operating a battery system is provided using high hydrogen capacity complex hydrides in an organic non-aqueous solvent that allows the transport of hydride ions such as AlH.sub.4.sup.- and metal ions during respective discharging and charging steps.

  14. Growth and decomposition of Lithium and Lithium hydride on Nickel

    DEFF Research Database (Denmark)

    Engbæk, Jakob; Nielsen, Gunver; Nielsen, Jane Hvolbæk;

    2006-01-01

    -hydride films. By only making thin films of LiH it is possible to study the stability of these hydride layers and compare it directly with the stability of pure Li without having any transport phenomena or adsorbed oxygen to obscure the results. The desorption of metallic lithium takes place at a lower...

  15. Hydrogen storage in the form of metal hydrides

    Science.gov (United States)

    Zwanziger, M. G.; Santana, C. C.; Santos, S. C.

    1984-01-01

    Reversible reactions between hydrogen and such materials as iron/titanium and magnesium/ nickel alloy may provide a means for storing hydrogen fuel. A demonstration model of an iron/titanium hydride storage bed is described. Hydrogen from the hydride storage bed powers a converted gasoline electric generator.

  16. Ultra-sonic observation in niobium hydride precipitation

    International Nuclear Information System (INIS)

    The hidrogen embrittlement of exothermic ocluders, had been considered as due to applied stress induced hydride precipitates leading to brittle fracture. The results of simultaneous measurements of macroscopic deformation and elastic change due to hydride precipitation, using the ultrasonic pulse-echo technique are showed. THen it was tested the possibility of kinectis precipitation parameters evoluation. (Author)

  17. Preferred hydride growth orientations on oxide-coated gadolinium surfaces

    International Nuclear Information System (INIS)

    Highlights: ► The preferred hydride growth orientations on gadolinium metal coated by a thin oxide layer are presented. ► A preferred growth of the (1 0 0)h plane of the face centered cubic (FCC) GdH2 is observed for the hydride spots forming below the oxidation layer. ► A change to the (1 1 1)h plane of the cubic hydride dominates for the hydride's Growth Centers. ► The texture change is attributed to the surface normal compressive stress component exerted by the oxidation layer on the developing hydride. - Abstract: The initial development of hydrides on polycrystalline gadolinium (Gd), as on some other hydride forming metals, is characterized by two sequential steps. The first step involves the rapid formation of a dense pattern of small hydride spots (referred to as the “small family” of hydrides) below the native oxidation layer. The second stage takes place when some of the “small family” nucleants (referred to as “growth centers”, GCs) break the oxide layer, leading to their rapid growth and finally to the massive hydriding of the sample. In the present study, the texture of the two hydride families was studied, by combining X-ray diffraction (XRD) analysis with a microscopic analysis of the hydride, using scanning electron microscopy (SEM) and atomic force microscopy (AFM). It has been observed that for the “small family”, a preferred growth of the (1 0 0)h plane of the cubic GdH2 takes place, whereas for the GCs, a change to the (1 1 1)h plane of the cubic hydride dominates. These preferred growth orientations were analyzed by their structure relation with the (0 0 .1)m basal plane of the Gd metal. It has been concluded that the above texture change is due to the surface normal compressive stress component exerted by the oxidation overlayer on the developing hydride, preventing the (0 0 .1)m||(1 1 1)h growth orientation. This stress is relieved upon the rupture of that overlayer and the development of the GCs, leading to the

  18. Modular hydride beds for mobile applications

    Energy Technology Data Exchange (ETDEWEB)

    Malinowski, M.E.; Stewart, K.D.

    1997-08-01

    Design, construction, initial testing and simple thermal modeling of modular, metal hydride beds have been completed. Originally designed for supplying hydrogen to a fuel cell on a mobile vehicle, the complete bed design consists of 8 modules and is intended for use on the Palm Desert Vehicle (PDV) under development at the Schatz Energy Center, Humbolt State University. Each module contains approximately 2 kg of a commercially available, low temperature, hydride-forming metal alloy. Waste heat from the fuel cell in the form of heated water is used to desorb hydrogen from the alloy for supplying feed hydrogen to the fuel cell. In order to help determine the performance of such a modular bed system, six modules were constructed and tested. The design and construction of the modules is described in detail. Initial testing of the modules both individually and as a group showed that each module can store {approximately} 30 g of hydrogen (at 165 PSIA fill pressure, 17 C), could be filled with hydrogen in 6 minutes at a nominal, 75 standard liters/min (slm) fueling rate, and could supply hydrogen during desorption at rates of 25 slm, the maximum anticipated hydrogen fuel cell input requirement. Tests made of 5 modules as a group indicated that the behavior of the group run in parallel both in fueling and gas delivery could be directly predicted from the corresponding, single module characteristics by using an appropriate scaling factor. Simple thermal modeling of a module as an array of cylindrical, hydride-filled tubes was performed. The predictions of the model are in good agreement with experimental data.

  19. Metal hydrides for concentrating solar thermal power energy storage

    Science.gov (United States)

    Sheppard, D. A.; Paskevicius, M.; Humphries, T. D.; Felderhoff, M.; Capurso, G.; Bellosta von Colbe, J.; Dornheim, M.; Klassen, T.; Ward, P. A.; Teprovich, J. A.; Corgnale, C.; Zidan, R.; Grant, D. M.; Buckley, C. E.

    2016-04-01

    The development of alternative methods for thermal energy storage is important for improving the efficiency and decreasing the cost of concentrating solar thermal power. We focus on the underlying technology that allows metal hydrides to function as thermal energy storage (TES) systems and highlight the current state-of-the-art materials that can operate at temperatures as low as room temperature and as high as 1100 °C. The potential of metal hydrides for thermal storage is explored, while current knowledge gaps about hydride properties, such as hydride thermodynamics, intrinsic kinetics and cyclic stability, are identified. The engineering challenges associated with utilising metal hydrides for high-temperature TES are also addressed.

  20. Helium trapping at erbium oxide precipitates in erbium hydride

    Energy Technology Data Exchange (ETDEWEB)

    Foiles, Stephen M. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Battaile, Corbett Chandler [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

    2016-02-01

    The formation of He bubbles in erbium tritides is a significant process in the aging of these materials. Due to the long-standing uncertainty about the initial nucleation process of these bubbles, there is interest in mechanisms that can lead to the localization of He in erbium hydrides. Previous work has been unable to identify nucleation sites in homogeneous erbium hydride. This work builds on the experimental observation that erbium hydrides have nano- scale erbium oxide precipitates due to the high thermodynamic stability of erbium oxide and the ubiquitous presence of oxygen during materials processing. Fundamental DFT calculations indicate that the He is energetically favored in the oxide relative to the bulk hydride. Activation energies for the motion of He in the oxide and at the oxide-hydride interface indicate that trapping is kinetically feasible. A simple kinetic Monte Carlo model is developed that demonstrates the degree of trapping of He as a function of temperature and oxide fraction.

  1. Low-frequency excitations in zirconium hydrides

    International Nuclear Information System (INIS)

    The slow inelastic neutron scattering (INS) on ZrHx systems (x = 0.38, 0.52) revealed new excitations located within the energy range 2-10 MeV. Besides the acoustic vibrations specific to α-HCP Zr and γ-FCO Zr hydride the fine structure of these excitations is clearly observed. The origin of the new observed peaks is not very clear but a proton tunneling or a resonance effect in α-Zr lattice could be taken into account

  2. Tritium immobilization and packaging using metal hydrides

    International Nuclear Information System (INIS)

    Tritium recovered from CANDU heavy water reactors will have to be packaged and stored in a safe manner. Tritium will be recovered in the elemental form, T2. Metal tritides are effective compounds in which to immobilize the tritium as a stable non-reactive solid with a high tritium capacity. The technology necessary to prepare hydrides of suitable metals, such as titanium and zirconium, have been developed and the properties of the prepared materials evaluated. Conceptual designs of packages for containing metal tritides suitable for transportation and long-term storage have been made and initial testing started. (author)

  3. Nanostructured Magnesium Hydride for Reversible Hydrogen Storage

    Science.gov (United States)

    de Rango, P.; Chaise, A.; Fruchart, D.; Miraglia, S.; Marty, Ph.

    2013-05-01

    The aim of this work was to develop suitable materials to store hydrogen in a solid state. A systematic investigation of the co-milling process of magnesium hydride with a transition metal was undertaken in order to produce nanostructured and highly reactive powders. The initiating role of the transition metal was evidenced by in situ neutron diffraction experiments. High performances in terms of thermal and mechanical behavior were achieved introducing expanded graphite and compacting the mixture to form composite materials. Absorption and desorption kinetics have been measured versus temperature and H2 pressure.

  4. Formation of hydrides blisters in zirconium alloys

    International Nuclear Information System (INIS)

    The formation of zirconium hydrides blisters in zirconium alloys due to the presence of a thermal gradient is a possible phenomenon which may occur in structural components of a reactor (pressure tubes), thus resulting a very important matter for the nuclear industry. For this reason, a series of experiments were initiated in the Hydrogen Damage Laboratory so as to obtain blisters of zirconium alloys and to study the aspects related to them. Zry-4 and Zr-2.5% Nb blisters were obtained. The propagation of a fissure present in a blister and the fracture surface were observed. The fissure propagated weakly in the blister and stopped in the Zry-4 matrix. (Author)

  5. Determination of silver and cerium in the liver and the kidney from a severely burned infant treated with silver sulfadiazine and cerium nitrate

    International Nuclear Information System (INIS)

    Silver and cerium in the liver and the kidney from severely burned infant were analyzed by neutron activation method. The patient was treated topically with cerium nitrate/silver sulfadiazine cream and cerium nitrate solution for 3 months. Then, the treatment with these drugs was stopped because o f abdominal distention. The patient died 1 month after the cessation of the treatment with these drugs. The tissue specimens, blank liver sample and reference standards were irradiated with TRIGA MARK II Reactor of Rikkyo University. About 1 month after the irradiation, the activities were measured with a Ge(Li) detector coupled to a 4096 channel pulse height analyzer. A large amount of silver was detected both in the liver and in the kidney and a trace of cerium only in the liver. A considerable amount of silver was detected in the liver and its quantity was about 1600 times more than that of normal livers reported by Hamilton, Minski and Cleary (1972 -- 73). Neither silver nor cerium were detected in the blank liver. These results suggest that prolonged topical chemotherapy of cerium nitrate/silver sulfadiazine cream and cerium nitrate solution for the extensive burn injuries causes considerable absorption of silver and cerium into the liver and the kidney. (author)

  6. [Determination of silver and cerium in the liver and the kidney from a severely burned infant treated with silver sulfadiazine and cerium nitrate].

    Science.gov (United States)

    Hirakawa, K

    1983-02-01

    Silver and cerium in the liver and the kidney from severely burned infant were analyzed by neutron activation method. The patient was treated topically with cerium nitrate/silver sulfadiazine cream and cerium nitrate solution for 3 months. Then, the treatment with these drugs was stopped because of abdominal distention. The patient died 1 month after the cessation of the treatment with these drugs. The tissue specimens, blank liver sample and reference standards were irradiated with TRIGA MARK II Reactor of Rikkyo University. About 1 month after the irradiation, the activities were measured with a Ge(Li) detector coupled to a 4096 channel pulse height analyzer. A large amount of silver was detected both in the liver and in the kidney and a trace of cerium only in the liver. A considerable amount of silver was detected in the liver and its quantity was about 1600 times more than that of normal livers reported by Hamilton, Minski and Cleary (1972-73). Neither silver nor cerium were detected in the blank liver. These results suggest that prolonged topical chemotherapy of cerium nitrate/silver sulfadiazine cream and cerium nitrate solution for the extensive burn injuries causes considerable absorption of silver and cerium into the liver and the kidney. PMID:6867381

  7. Determination of silver and cerium in the liver and the kidney from a severely burned infant treated with silver sulfadiazine and cerium nitrate

    Energy Technology Data Exchange (ETDEWEB)

    Hirakawa, Keiko (Nippon Medical School, Tokyo)

    1983-02-01

    Silver and cerium in the liver and the kidney from severely burned infant were analyzed by neutron activation method. The patient was treated topically with cerium nitrate/silver sulfadiazine cream and cerium nitrate solution for 3 months. Then, the treatment with these drugs was stopped because of abdominal distention. The patient died 1 month after the cessation of the treatment with these drugs. The tissue specimens, blank liver sample and reference standards were irradiated with TRIGA MARK II Reactor of Rikkyo University. About 1 month after the irradiation, the activities were measured with a Ge(Li) detector coupled to a 4096 channel pulse height analyzer. A large amount of silver was detected both in the liver and in the kidney and a trace of cerium only in the liver. A considerable amount of silver was detected in the liver and its quantity was about 1600 times more than that of normal livers reported by Hamilton, Minski and Cleary (1972 -- 73). Neither silver nor cerium were detected in the blank liver. These results suggest that prolonged topical chemotherapy of cerium nitrate/silver sulfadiazine cream and cerium nitrate solution for the extensive burn injuries causes considerable absorption of silver and cerium into the liver and the kidney.

  8. Hydrogen in novel solid-state metal hydrides

    International Nuclear Information System (INIS)

    Solid-state metal hydrides display hydrogen densities close to that of liquid hydrogen and thus provide a safe and efficient way of storing hydrogen. As a result of recent neutron and synchrotron diffraction work some novel metal hydrides have been characterized that shed new light on the nature of metal-hydrogen interactions. While hydrogen appears as an anion surrounded by a large inventory of cation configurations in ionic hydrides such as Ca4Mg3H14, Ca19Mg8H54, Eu2MgD6, Eu6Mg7D26 and Eu2Mg3D10, it acts as a terminal ligand in covalently bonded hydride complexes based on p-elements such as [BH4]- and d-elements such as [IrH5]4- and [IrH4]5- in the complex hydrides LiBH4 and Mg6Ir2H11, respectively. Surprisingly, hydride complexes and hydride anions can also be discerned in typically metallic (interstitial) hydrides such as NdMgNi4H4 (= Nd3+Mg+2.[Ni4H4]5-) and LaMg2NiD7 (= La3+Mg+22.[NiH4]4-.3H-). Some hydrides also reveal other interesting features such as a hydrogenation induced Ce4+→Ce3+ valence change in CeMn1.8Al0.2H4.4 at room temperature that is accompanied by a Mn/Al metal atom exchange over distances of ∝2.6 A, and a hydrogen induced metal-to-nonmetal transition near ambient conditions that leads from the metallic compound Mg3Ir to the red colored hydride Mg6Ir2H11. In this article recent work and some methodological aspects are highlighted. (orig.)

  9. Results of NDE Technique Evaluation of Clad Hydrides

    Energy Technology Data Exchange (ETDEWEB)

    Dennis C. Kunerth

    2014-09-01

    This report fulfills the M4 milestone, M4FT-14IN0805023, Results of NDE Technique Evaluation of Clad Hydrides, under Work Package Number FT-14IN080502. During service, zirconium alloy fuel cladding will degrade via corrosion/oxidation. Hydrogen, a byproduct of the oxidation process, will be absorbed into the cladding and eventually form hydrides due to low hydrogen solubility limits. The hydride phase is detrimental to the mechanical properties of the cladding and therefore it is important to be able to detect and characterize the presence of this constituent within the cladding. Presently, hydrides are evaluated using destructive examination. If nondestructive evaluation techniques can be used to detect and characterize the hydrides, the potential exists to significantly increase test sample coverage while reducing evaluation time and cost. To demonstrate the viability this approach, an initial evaluation of eddy current and ultrasonic techniques were performed to demonstrate the basic ability to these techniques to detect hydrides or their effects on the microstructure. Conventional continuous wave eddy current techniques were applied to zirconium based cladding test samples thermally processed with hydrogen gas to promote the absorption of hydrogen and subsequent formation of hydrides. The results of the evaluation demonstrate that eddy current inspection approaches have the potential to detect both the physical damage induced by hydrides, e.g. blisters and cracking, as well as the combined effects of absorbed hydrogen and hydride precipitates on the electrical properties of the zirconium alloy. Similarly, measurements of ultrasonic wave velocities indicate changes in the elastic properties resulting from the combined effects of absorbed hydrogen and hydride precipitates as well as changes in geometry in regions of severe degradation. However, for both approaches, the signal responses intended to make the desired measurement incorporate a number of contributing

  10. Development of hydride absorber for fast reactor. Application of hafnium hydride to control rod of large fast reactor

    International Nuclear Information System (INIS)

    The application of hafnium hydride (Hf-hydride) to a control rod for a large fast reactor where the B4C control rod is originally employed is studied. Three types of Hf-hydride control rods are designed. The control rod worth and its change during the burnup are evaluated for different hydrogen-to-hafnium ratios and are compared with those of the original B4C control rod. The result indicates that the worths of the Hf-hydride and the 10B-enriched B4C control rods are approximately the same, and the lifetime of the Hf-hydride control rod is almost four times longer than that of the 10B-enriched B4C control rod. The core performances of the shutdown margin, sodium void reactivity, Doppler reactivity coefficient, and breeding ratio are analyzed. It is indicated that those for the Hf-hydride control rod are almost the same as those for the original B4C control rod. The behavior of neutrons moderated by the Hf-hydride control rod is analyzed. It is confirmed that the Hf-hydride control rod does not cause any thermal spike problems in the fast reactor core. (author)

  11. Nanoindentation measurements of the mechanical properties of zirconium matrix and hydrides in unirradiated pre-hydrided nuclear fuel cladding

    Energy Technology Data Exchange (ETDEWEB)

    Rico, A., E-mail: alvaro.rico@urjc.es [DIMME, Departamento de Tecnología Mecánica, Universidad Rey Juan Carlos, c/Tulipán s/n, E-28933 Móstoles, Madrid (Spain); Martin-Rengel, M.A., E-mail: mamartin@mater.upm.es [Departamento de Ciencia de los Materiales, UPM, E.T.S.I. Caminos, Canales y Puertos, Profesor Aranguren SN, E-28040 Madrid (Spain); Ruiz-Hervias, J., E-mail: jesus.ruiz@upm.es [Departamento de Ciencia de los Materiales, UPM, E.T.S.I. Caminos, Canales y Puertos, Profesor Aranguren SN, E-28040 Madrid (Spain); Rodriguez, J. [DIMME, Departamento de Tecnología Mecánica, Universidad Rey Juan Carlos, c/Tulipán s/n, E-28933 Móstoles, Madrid (Spain); Gomez-Sanchez, F.J., E-mail: javier.gomez@amsimulation.com [Advanced Material Simulation, S.L, Madrid (Spain)

    2014-09-15

    It is well known that the mechanical properties of the nuclear fuel cladding may be affected by the presence of hydrides. The average mechanical properties of hydrided cladding have been extensively investigated from a macroscopic point of view. In addition, the mechanical and fracture properties of bulk hydride samples fabricated from zirconium plates have also been reported. In this paper, Young’s modulus, hardness and yield stress are measured for each phase, namely zirconium hydrides and matrix, of pre-hydrided nuclear fuel cladding. To this end, nanoindentation tests were performed on ZIRLO samples in as-received state, on a hydride blister and in samples with 150 and 1200 ppm of hydrogen homogeneously distributed along the hoop direction of the cladding. The results show that the measured mechanical properties of the zirconium hydrides and ZIRLO matrix (Young’s modulus, hardness and yield stress) are rather similar. From the experimental data, the hydride volume fraction in the cladding samples with 150 and 1200 ppm was estimated and the average mechanical properties were calculated by means of the rule of mixtures. These values were compared with those obtained from ring compression tests. Good agreement between the results obtained by both methods was found.

  12. Fundamental aspects of regenerative cerium oxide nanoparticles and their applications in nanobiotechnology

    Science.gov (United States)

    Patil, Swanand D.

    Cerium oxide has been used extensively for various applications over the past two decades. The use of cerium oxide nanoparticles is beneficial in present applications and can open avenues for future applications. The present study utilizes the microemulsion technique to synthesize uniformly distributed cerium oxide nanoparticles. The same technique was also used to synthesize cerium oxide nanoparticles doped with trivalent elements (La and Nd). The fundamental study of cerium oxide nanoparticles identified variations in properties as a function of particle size and also due to doping with trivalent elements (La and Nd). It was found that the lattice parameter of cerium oxide nanoparticles increases with decrease in particle size. Also Raman allowed mode shift to lower energies and the peak at 464 cm-1 becomes broader and asymmetric. The size dependent changes in cerium oxide were correlated to increase in oxygen vacancy concentration in the cerium oxide lattice. The doping of cerium oxide nanoparticles with trivalent elements introduces more oxygen vacancies and expands the cerium oxide lattice further (in addition to the lattice expansion due to the size effect). The lattice expansion is greater for La-doped cerium oxide nanoparticles compared to Nd-doping due to the larger ionic radius of La compared to Nd, the lattice expansion is directly proportional to the dopant concentration. The synthesized cerium oxide nanoparticles were used to develop an electrochemical biosensor of hydrogen peroxide (H2O2). The sensor was useful to detect H2O2 concentrations as low as 1muM in water. Also the preliminary testing of the sensor on tomato stem and leaf extracts indicated that the sensor can be used in practical applications such as plant physiological studies etc. The nanomolar concentrations of cerium oxide nanoparticles were also found to be useful in decreasing ROS (reactive oxygen species) mediated cellular damages in various in vitro cell cultures. Cerium oxide

  13. Synthesis and crystal kinetics of cerium oxide nanocrystallites prepared by co-precipitation process

    Energy Technology Data Exchange (ETDEWEB)

    Shih, C.J., E-mail: cjshih@kmu.edu.tw [Department of Fragrance and Cosmetics Science, Kaohsiung Medical University, 100 Shi-Chuan 1st Road, Kaohsiung 807, Taiwan (China); Chen, Y.J. [Institute of Biomedical Sciences, National Sun Yat-Sen University, Kaohsiung 804, Taiwan (China); Hon, M.H. [Department of Materials Science and Engineering, National Cheng Kung University, Tainan 701, Taiwan (China)

    2010-05-15

    Cerium oxide nanocrystallites were synthesized at a relatively low temperature using cerium nitrate as starting materials in a water solution by a co-precipitation process. Effect of calcination temperature on the crystallite growth of cerium oxide nano-powders was investigated by X-ray diffraction, transmission electron microscopy and electron diffraction. The crystallization temperature of the cerium oxide powders was estimated to be about 273 K by XRD analysis. When calcined from 473 to 1273 K, the crystallization of the face-centered cubic phase was observed by XRD. The crystallite size of the cerium oxide increased from 10.0 to 43.8 nm with calcining temperature increasing from 673 to 1273 K. The activation energy for growth of cerium oxide nanoparticles was found to be 16.0 kJ mol{sup -1}.

  14. Synthesis and crystal kinetics of cerium oxide nanocrystallites prepared by co-precipitation process

    International Nuclear Information System (INIS)

    Cerium oxide nanocrystallites were synthesized at a relatively low temperature using cerium nitrate as starting materials in a water solution by a co-precipitation process. Effect of calcination temperature on the crystallite growth of cerium oxide nano-powders was investigated by X-ray diffraction, transmission electron microscopy and electron diffraction. The crystallization temperature of the cerium oxide powders was estimated to be about 273 K by XRD analysis. When calcined from 473 to 1273 K, the crystallization of the face-centered cubic phase was observed by XRD. The crystallite size of the cerium oxide increased from 10.0 to 43.8 nm with calcining temperature increasing from 673 to 1273 K. The activation energy for growth of cerium oxide nanoparticles was found to be 16.0 kJ mol-1.

  15. Effect of cerium modification on microstructure and properties of hypereutectic high chromium cast iron

    Energy Technology Data Exchange (ETDEWEB)

    Zhi, Xiaohui, E-mail: mkmkzxh@hotmail.com [School of Mechanical Engineering, Shijiazhuang Tiedao University, Shijiazhuang 050043, Hebei Province (China); Liu, Jinzhi [School of Mechanical Engineering, Shijiazhuang Tiedao University, Shijiazhuang 050043, Hebei Province (China); Xing, Jiandong; Ma, Shengqiang [State Key Laboratory Mechanical Behavior of Materials, School of Materials Science and Engineering, Xi' an Jiaotong University, Xi' an 710049, Shaanxi Province (China)

    2014-05-01

    The effect of cerium modification on the microstructure and properties of hypereutectic high chromium cast iron primarily containing 4.0 wt% C and 20.0 wt% Cr was studied by means of optical microscopy, transmission electron microscope, scanning electron microscope, and energy dispersive X-ray spectrometry. The primary M{sub 7}C{sub 3} carbides were refined obviously when cerium was added in the melt. Ce{sub 2}S{sub 3} was found in the primary M{sub 7}C{sub 3} carbides and acted as the heterogeneous substrate of M{sub 7}C{sub 3} carbides. The impact toughness of the specimen modified with 0.5 wt% cerium increased by 50% compared with the specimen without cerium modification. The hardness of the alloy modified with cerium increased slightly compared with the specimen without cerium modification.

  16. Neutron scattering on hydrides of intermetallic compounds

    International Nuclear Information System (INIS)

    This review surveys the application of neutron scattering for the investigation of the microscopic behaviour of hydrogen in intermetallic compounds. This concerns the structure as well as the dynamics. Neutron diffraction experiments were performed on Ti1.2Mn1.8D3 and LaNi5D7. In the latter case the dominant nickel scattering could be suppressed by isotope substitution with 60Ni, and the anisotropic broadening of the Bragg peaks could be modelled in a correspondingly modified Rietveld-profile refinement. For the investigation of hydrogen diffusion in intermetallic hydrides by means of quasielastic neutron scattering an iterative multiple scattering correction procedure has been developped which allows a reliable determination of hydrogen diffusion coefficients. The mechanism of hydrogen diffusion in intermetallic hydrides comprises three types of jumps: escape jumps out of energetically lower interstitials, transport jumps over the energetically higher sites and locally restricted jump processes. For Ti1.2Mn1.8H3 the main features of the diffusional behaviour could be described quantitatively in the framework of a three state model. By means of neutron vibrational spectroscopy information about the occupied hydrogen sites and thus about the structure can be extracted from the symmetry splitting of the vibrational modes. In this way we showed that in α-LaNi5Hx, La2Ni4-octahedral and La2Ni2-tetrahedral interstitial sites are occupied. (orig./GG)

  17. Millimeter-Wave Spectroscopy of Ethylmercury Hydride

    Science.gov (United States)

    Goubet, M.; Motiyenko, R. A.; Margulès, L.; Guillemin, J.-C.

    2012-06-01

    The first millimeter-wave rotational spectrum of an organomercury compound, ethylmercury hydride (CH_3CH_2HgH), has been recorded using the Lille fast-scan spectrometer in the frequency range 120 -- 180 GHz. The spectroscopic study is complemented by quantum chemical calculations taking into account relativistic effects on the mercury atom. The very good agreement between theoretical and experimental molecular parameters validates the chosen ab initio method, in particular its capability to predict the accurate values of the quartic centrifugal distortion constants related to this type of compound. Estimations of the nuclear quadrupole coupling constants are not as predictive as the structural parameters but good enough to satisfy the spectroscopic needs. In addition, the orientation of the H--Hg--C bonds axis deduced from the experimental nuclear quadrupole coupling constants compares well with the corresponding ab initio value. From the good agreement between experimental and theoretical results, together with the observation of the six most abundant isotopes of mercury, ethylmercury hydride is unambiguously identified and its calculated equilibrium geometry is confirmed. Alekseev, E.A. et al. Radio Physics and Radio Astronomy 3 (2012) 78.

  18. NATO Advanced Study Institute on Metal Hydrides

    CERN Document Server

    1981-01-01

    In the last five years, the study of metal hydrides has ex­ panded enormously due to the potential technological importance of this class of materials in hydrogen based energy conversion schemes. The scope of this activity has been worldwide among the industrially advanced nations. There has been a consensus among researchers in both fundamental and applied areas that a more basic understanding of the properties of metal/hydrogen syster;,s is required in order to provide a rational basis for the selection of materials for specific applications. The current worldwide need for and interest in research in metal hydrides indicated the timeliness of an Advanced Study Insti­ tute to provide an in-depth view of the field for those active in its various aspects. The inclusion of speakers from non-NATO coun­ tries provided the opportunity for cross-fertilization of ideas for future research. While the emphasis of the Institute was on basic properties, there was a conscious effort to stimulate interest in the applic...

  19. Metal hydrides for lithium-ion batteries.

    Science.gov (United States)

    Oumellal, Y; Rougier, A; Nazri, G A; Tarascon, J-M; Aymard, L

    2008-11-01

    Classical electrodes for Li-ion technology operate via an insertion/de-insertion process. Recently, conversion electrodes have shown the capability of greater capacity, but have so far suffered from a marked hysteresis in voltage between charge and discharge, leading to poor energy efficiency and voltages. Here, we present the electrochemical reactivity of MgH(2) with Li that constitutes the first use of a metal-hydride electrode for Li-ion batteries. The MgH(2) electrode shows a large, reversible capacity of 1,480 mAh g(-1) at an average voltage of 0.5 V versus Li(+)/Li(o) which is suitable for the negative electrode. In addition, it shows the lowest polarization for conversion electrodes. The electrochemical reaction results in formation of a composite containing Mg embedded in a LiH matrix, which on charging converts back to MgH(2). Furthermore, the reaction is not specific to MgH(2), as other metal or intermetallic hydrides show similar reactivity towards Li. Equally promising, the reaction produces nanosized Mg and MgH(2), which show enhanced hydrogen sorption/desorption kinetics. We hope that such findings can pave the way for designing nanoscale active metal elements with applications in hydrogen storage and lithium-ion batteries. PMID:18849978

  20. Synthesis and hydride transfer reactions of cobalt and nickel hydride complexes to BX3 compounds.

    Science.gov (United States)

    Mock, Michael T; Potter, Robert G; O'Hagan, Molly J; Camaioni, Donald M; Dougherty, William G; Kassel, W Scott; DuBois, Daniel L

    2011-12-01

    Hydrides of numerous transition metal complexes can be generated by the heterolytic cleavage of H(2) gas such that they offer alternatives to using main group hydrides in the regeneration of ammonia borane, a compound that has been intensely studied for hydrogen storage applications. Previously, we reported that HRh(dmpe)(2) (dmpe = 1,2-bis(dimethylphosphinoethane)) was capable of reducing a variety of BX(3) compounds having a hydride affinity (HA) greater than or equal to the HA of BEt(3). This study examines the reactivity of less expensive cobalt and nickel hydride complexes, HCo(dmpe)(2) and [HNi(dmpe)(2)](+), to form B-H bonds. The hydride donor abilities (ΔG(H(-))°) of HCo(dmpe)(2) and [HNi(dmpe)(2)](+) were positioned on a previously established scale in acetonitrile that is cross-referenced with calculated HAs of BX(3) compounds. The collective data guided our selection of BX(3) compounds to investigate and aided our analysis of factors that determine favorability of hydride transfer. HCo(dmpe)(2) was observed to transfer H(-) to BX(3) compounds with X = H, OC(6)F(5), and SPh. The reaction with B(SPh)(3) is accompanied by the formation of dmpe-(BH(3))(2) and dmpe-(BH(2)(SPh))(2) products that follow from a reduction of multiple B-SPh bonds and a loss of dmpe ligands from cobalt. Reactions between HCo(dmpe)(2) and B(SPh)(3) in the presence of triethylamine result in the formation of Et(3)N-BH(2)SPh and Et(3)N-BH(3) with no loss of a dmpe ligand. Reactions of the cationic complex [HNi(dmpe)(2)](+) with B(SPh)(3) under analogous conditions give Et(3)N-BH(2)SPh as the final product along with the nickel-thiolate complex [Ni(dmpe)(2)(SPh)](+). The synthesis and characterization of HCo(dedpe)(2) (dedpe = Et(2)PCH(2)CH(2)PPh(2)) from H(2) and a base is also discussed, including the formation of an uncommon trans dihydride species, trans-[(H)(2)Co(dedpe)(2)][BF(4)]. PMID:22040085

  1. Critical indices for reversible gamma-alpha phase transformation in metallic cerium

    Science.gov (United States)

    Soldatova, E. D.; Tkachenko, T. B.

    1980-08-01

    Critical indices for cerium have been determined within the framework of the pseudobinary solution theory along the phase equilibrium curve, the critical isotherm, and the critical isobar. The results obtained verify the validity of relationships proposed by Rushbrook (1963), Griffiths (1965), and Coopersmith (1968). It is concluded that reversible gamma-alpha transformation in metallic cerium is a critical-type transformation, and cerium has a critical point on the phase diagram similar to the critical point of the liquid-vapor system.

  2. The effect of cerium valence states at cerium oxide nanoparticle surfaces on cell proliferation

    KAUST Repository

    Naganuma, Tamaki

    2014-05-01

    Understanding and controlling cell proliferation on biomaterial surfaces is critical for scaffold/artificial-niche design in tissue engineering. The mechanism by which underlying integrin ligates with functionalized biomaterials to induce cell proliferation is still not completely understood. In this study, poly-l-lactide (PL) scaffold surfaces were functionalized using layers of cerium oxide nanoparticles (CNPs), which have recently attracted attention for use in therapeutic application due to their catalytic ability of Ce4+ and Ce3+ sites. To isolate the influence of Ce valance states of CNPs on cell proliferation, human mesenchymal stem cells (hMSCs) and osteoblast-like cells (MG63) were cultured on the PL/CNP surfaces with dominant Ce4+ and Ce3+ regions. Despite cell type (hMSCs and MG63 cells), different surface features of Ce4+ and Ce3+ regions clearly promoted and inhibited cell spreading, migration and adhesion behavior, resulting in rapid and slow cell proliferation, respectively. Cell proliferation results of various modified CNPs with different surface charge and hydrophobicity/hydrophilicity, indicate that Ce valence states closely correlated with the specific cell morphologies and cell-material interactions that trigger cell proliferation. This finding suggests that the cell-material interactions, which influence cell proliferation, may be controlled by introduction of metal elements with different valence states onto the biomaterial surface. © 2014 Elsevier Ltd.

  3. Effect of metal hydrides on the burning characteristics of boron

    International Nuclear Information System (INIS)

    Highlights: • The effect of some metal hydrides on the burning characteristics of boron is studied for the first time. • We are the first to conduct a TG experiment on boron samples at high temperatures (a maximum of 1750 °C). • The thermal reaction process of boron is firstly divided into five stages according to the weight gain rate of the sample. • Specific values of metal hydrides on ignition delay time and combustion intensity of boron are obtained. - Abstract: In this study, the effect of four metal hydrides on the burning characteristics of boron was investigated. Thermogravimetric experiment results show that the thermal reaction process of boron samples can be divided into five stages. The thermal reactions of boron can be significantly promoted with LiH, which can reduce the initial temperature of the first violent reaction stage by ∼140 °C. The starting temperature of the post-reaction stage also decreases by ∼260 °C. The results of the laser ignition experiment suggest that all four metal hydrides can promote boron burning. Nonetheless, different metal hydrides display varied promotional effects. Among the studied hydrides, LiH is the most effective additive and shortens the ignition delay time of boron by ∼34.1%. Moreover, it enhances the combustion intensity of boron by ∼117.6%. The other three metal hydrides (CaH2, TiH2, and ZrH2) can also contribute to boron burning

  4. Zircaloy-4 hydriding. Hydrogen distribution in PWR's rod cladding

    International Nuclear Information System (INIS)

    In pressurised water reactors, Zircaloy 4 is used as fuel cladding in contact with hot water. The precipitation of hydrides at room temperatures causes mechanical deterioration of the cladding. As the cladding is subjected to a radial temperature gradient, the hydrogen distribution is greatly affected. The image analysis method is used to determine the hydride distribution in the irradiated cladding. To calibrate this method, a device was specially built for the preparation of Zircaloy specimens with known hydrogen contents. The hydriding conditions and hydrogen content determination procedures were fixed. We have successfully realized specimens with various hydrogen contents. With these specimens, a relationship between the parameter Sv (surface density of hydrides) and the hydrogen content was established. This parameter Sv is independent from the Zircaloy 4 metallurgical state (i.e. stress relieved or recrystallized) and from the analysis section (longitudinal or transverse). Study of hydrogen content and hydride distribution in irradiated cladding by means of image analysis showed that the method is limited by its ability of separation between neighbouring hydrides at cladding's periphery where the hydrogen content can reach several thousands ppm. Nevertheless, this method gives us some information about hydride distribution inside the cladding. A model for thermal diffusion was developped to stimulate the migration of hydrogen in Zirconium alloys. This model was used to predict hydrogen distribution in the irradiated cladding. Comparison of model predictions with results of image analysis shows good agreement. (Author). refs., figs., tabs

  5. Isotope exchange between gaseous hydrogen and uranium hydride powder

    International Nuclear Information System (INIS)

    Highlights: • Isotope exchange between hydrogen gas and uranium hydride powder can be rapid and reversible. • Gas–solid exchange rate is controlled by transport within ∼0.7 μm hydride particles. • Gas chromatographic separation of hydrogen isotopes using uranium hydride is feasible. - Abstract: Isotope exchange between gaseous hydrogen and solid uranium hydride has been studied by flowing hydrogen (deuterium) gas through packed powder beds of uranium deuteride (hydride). We used a residual gas analyzer system to perform real-time analysis of the effluent gas composition. We also developed an exchange and transport model and, by fitting it to the experimental data, extracted kinetic parameters for the isotope exchange reaction. Our results suggest that, from approximately 70 to 700 kPa and 25 to 400 °C, the gas-to-solid exchange rate is controlled by hydrogen and deuterium transport within the ∼0.7 μm diameter uranium hydride particles. We use our kinetic parameters to show that gas chromatographic separation of hydrogen and deuterium using uranium hydride could be feasible

  6. Study of cerium diffusion in undoped lithium-6 enriched glass with Rutherford backscattering spectrometry

    Science.gov (United States)

    Zhang, Xiaodong; Moore, Michael E.; Lee, Kyung-Min; Lukosi, Eric D.; Hayward, Jason P.

    2016-07-01

    Undoped lithium-6 enriched glasses coated with pure cerium (99.9%) with a gold protection layer on top were heated at three different temperatures (500, 550, and 600 °C) for varied durations (1, 2, and 4 h). Diffusion profiles of cerium in such glasses were obtained with the conventional Rutherford backscattering technique. Through fitting the diffusion profiles with the thin-film solution of Fick's second law, diffusion coefficients of cerium with different annealing temperatures and durations were solved. Then, the activation energy of cerium for the diffusion process in the studied glasses was found to be 114 kJ/mol with the Arrhenius equation.

  7. Doping of KDP single crystals with cerium: Growth and optical properties

    International Nuclear Information System (INIS)

    The features of doping of KDP crystals with cerium ions and organocerium complexes with alizarin complexon and arsenazo III have been investigated. It is established that 'direct' doping by introducing cerium salts into the initial solution cannot be implemented. The effect of organometallic complexes of cerium on the crystal growth has been studied. Organocerium complexes predominantly enter the prismatic or pyramidal growth sectors. It is shown that the complex arsenazo III + Ce blocks the growth of the prismatic sector. Cerium-doped KDP crystals exhibit a photoluminescence band peaking at the wavelength λmax= 350 nm.

  8. The development of metal hydrides using as concentrating solar thermal storage materials

    Science.gov (United States)

    Qu, Xuanhui; Li, Yang; Li, Ping; Wan, Qi; Zhai, Fuqiang

    2015-12-01

    Metal hydrides high temperature thermal heat storage technique has great promising future prospects in solar power generation, industrial waste heat utilization and peak load regulating of power system. This article introduces basic principle of metal hydrides for thermal storage, and summarizes developments in advanced metal hydrides high-temperature thermal storage materials, numerical simulation and thermodynamic calculation in thermal storage systems, and metal hydrides thermal storage prototypes. Finally, the future metal hydrides high temperature thermal heat storage technique is been looked ahead.

  9. Fabrication of mesoporous cerium dioxide films by cathodic electrodeposition.

    Science.gov (United States)

    Kim, Young-Soo; Lee, Jin-Kyu; Ahn, Jae-Hoon; Park, Eun-Kyung; Kim, Gil-Pyo; Baeck, Sung-Hyeon

    2007-11-01

    Mesoporous cerium dioxide (Ceria, CeO2) thin films have been successfully electrodeposited onto ITO-coated glass substrates from an aqueous solution of cerium nitrate using CTAB (Cetyltrimethylammonium Bromide) as a templating agent. The synthesized films underwent detailed characterizations. The crystallinity of synthesized CeO2 film was confirmed by XRD analysis and HR-TEM analysis, and surface morphology was investigated by SEM analysis. The presence of mesoporosity in fabricated films was confirmed by TEM and small angle X-ray analysis. As-synthesized film was observed from XRD analysis and HR-TEM image to have well-crystallized structure of cubic phase CeO2. Transmission electron microscopy and small angle X-ray analysis revealed the presence of uniform mesoporosity with a well-ordered lamellar phase in the CeO2 films electrodeposited with CTAB templating. PMID:18047150

  10. Antioxidant activity of levan coated cerium oxide nanoparticles.

    Science.gov (United States)

    Kim, Sun-Jung; Chung, Bong Hyun

    2016-10-01

    Levan coated cerium oxide nanoparticles (LCNPs) with the enhanced antioxidant activity were successfully synthesized and characterized. Levan and their derivatives are attractive for biomedical applications attributable to their antioxidant, anti-inflammation and anti-tumor properties. LCNPs were synthesized using the one-pot and green synthesis system with levan. For production of nanoparticles, levan plays a role as a stabilizing and reducing agent. Fourier transform infrared spectroscopy (FT-IR) analysis showed that LCNPs successfully synthesized. The morphology and size of nanoparticles were confirmed by transmission electron microscopy (TEM) and dynamic light scattering (DLS). LCNPs have good water solubility and stability. The conjugation of levan with cerium oxide nanoparticles improved antioxidant activity. Moreover the level of ROS was reduced after treatment of LCNPs to H2O2 stimulated NIH3T3 cells. These results demonstrate that the LCNPs are useful for applying of treatment of ROS induced diseases. PMID:27312651

  11. Adsorption of Fluoride Ion by Inorganic Cerium Based Adsorbent

    Institute of Scientific and Technical Information of China (English)

    Jiao Zhongzhi(焦中志); Chen Zhonglin; Yang Min; Zhang Yu; Li Guibai

    2004-01-01

    Excess of fluoride in drinking water is harmful to human health, the concentration of F- ions must be maintained in the range of 0.5 to 1.5 mg/L. An inorganic cerium based adsorbent (CTA) is developed on the basis of research of adsorption of fluoride on cerium oxide hydrate. Some adsorption of fluoride by CTA adsorbent experiments were carried out, and results showed that CTA adsorbent has a quick adsorption speed and a large adsorption capacity. Adsorption follows Freundlich isotherm, and low pH value helps fluoride removal. Some physical-chemical characteristics of CTA adsorbent were experimented, fluoride removal mechanism was explored, and results showed that hydroxyl group of CTA adsorbent played an important role in the fluoride removal.

  12. Development of a zinc-cerium redox flow battery

    OpenAIRE

    Leung, P. K.

    2011-01-01

    Redox flow batteries (RFBs) can be used to store energy on the large and medium scale (kW – MW), particularly in applications such as load levelling of electrical power supplies, power quality control application and facilitating renewable energy deployment. In this thesis, the development of a divided and undivided zinc-cerium redox flow battery from its fundamental chemistry in aqueous methanesulfonic acid has been described. This comprehensive investigation has focused on th...

  13. Purification of cerium, neodymium and gadolinium for low background experiments

    OpenAIRE

    Boiko R.S.; Barabash A.S.; Belli P.; Bernabei R.; Cappella F.; Cerulli R.; Danevich F.A.; Incicchitti A.; Laubenstein M.; Mokina V.M.; Nisi S.; Poda D.V.; Polischuk O.G.; Tretyak V.I.

    2014-01-01

    Cerium, neodymium and gadolinium contain double beta active isotopes. The most interesting are 150Nd and 160Gd (promising for 0ν2β search), 136Ce (2β+ candidate with one of the highest Q2β). The main problem of compounds containing lanthanide elements is their high radioactive contamination by uranium, radium, actinium and thorium. The new generation 2β experiments require development of methods for a deep purification of lanthanides from the radioactive elements. A combination of physical an...

  14. Properties of ceramics based on cerium dioxide with crystalline filaments

    International Nuclear Information System (INIS)

    Problems of the increase of thermal resistance of ceramics on the basis of cerium dioxide with the interduction of filamentous crystals (FC) of CeO2 and MgO have been considered. It is established that FC of MgO and CeO2 are dissolved in the matrix, foAming fine oblong pores, promoting relaxation of thermal strains and preventing crack propagation, which increases the material thermal resistance

  15. Far infrared properties of PbTe doped with cerium

    Energy Technology Data Exchange (ETDEWEB)

    Nikolic, P.M. [Institute of Technical Sciences SASA, Knez Mihailova 35/IV, 11000 Belgrade (Serbia)]. E-mail: nikolic@sanu.ac.yu; Koenig, W. [Max Planck Institut fuer Festkoerperforschung, Heisenbergstrasse 1, 7000 Stuttgart 80 (Germany); Vujatovic, S.S. [Institute of Technical Sciences SASA, Knez Mihailova 35/IV, 11000 Belgrade (Serbia); Blagojevic, V. [Faculty of Electronic Engineering, University of Belgrade, Bulevar Kralja Aleksandra 73, 11000 Belgrade (Serbia); Lukovic, D. [Institute of Technical Sciences SASA, Knez Mihailova 35/IV, 11000 Belgrade (Serbia); Savic, S. [Institute of Technical Sciences SASA, Knez Mihailova 35/IV, 11000 Belgrade (Serbia); Radulovic, K. [Institute of Technical Sciences SASA, Knez Mihailova 35/IV, 11000 Belgrade (Serbia); Urosevic, D. [Mathematical Institute SASA, Knez Mihailova 35/I, 11000 Belgrade (Serbia); Nikolic, M.V. [Center for Multidisciplinary Studies of the University of Belgrade, Kneza Viseslava 1, Belgrade (Serbia)

    2007-05-16

    Single crystal samples of lead telluride doped with cerium were made using the Bridgman method. Far infrared reflectivity spectra in the temperature range from 10 to 300 K are presented. The experimental data were numerically analyzed using a fitting procedure based on the plasmon-phonon interaction model and optical parameters were determined. Two additional local modes were observed at about 138 and 337 cm{sup -1}. The origin of these local vibrational impurity modes was discussed.

  16. Antioxidant Cerium Oxide Nanoparticles in Biology and Medicine

    OpenAIRE

    Nelson, Bryant C.; Monique E. Johnson; Walker, Marlon L.; Riley, Kathryn R.; Christopher M. Sims

    2016-01-01

    Previously, catalytic cerium oxide nanoparticles (CNPs, nanoceria, CeO2-x NPs) have been widely utilized for chemical mechanical planarization in the semiconductor industry and for reducing harmful emissions and improving fuel combustion efficiency in the automobile industry. Researchers are now harnessing the catalytic repertoire of CNPs to develop potential new treatment modalities for both oxidative- and nitrosative-stress induced disorders and diseases. In order to reach the point where o...

  17. Monomers, Dimers, and Helices: Complexities of Cerium and Plutonium Phenanthrolinecarboxylates.

    Science.gov (United States)

    Cary, Samantha K; Ferrier, Maryline G; Baumbach, Ryan E; Silver, Mark A; Lezama Pacheco, Juan; Kozimor, Stosh A; La Pierre, Henry S; Stein, Benjamin W; Arico, Alexandra A; Gray, Danielle L; Albrecht-Schmitt, Thomas E

    2016-05-01

    The reaction of Ce(III) or Pu(III) with 1,10-phenanthroline-2,9-dicarboxylic acid (PDAH2) results in the formation of new f-element coordination complexes. In the case of cerium, Ce(PDA)(H2O)2Cl·H2O (1) or [Ce(PDAH)(PDA)]2[Ce(PDAH)(PDA)] (2) was isolated depending on the Ce/ligand ratio in the reaction. The structure of 2 is composed of two distinct substructures that are constructed from the same monomer. This monomer is composed of a Ce(III) cation bound by one PDA(2-) dianionic ligand and one PDAH(-) monoanionic ligand, both of which are tetradentate. Bridging by the carboxylate moieties leads to either [Ce(PDAH)(PDA)]2 dimers or [Ce(PDAH)(PDA)]1∞ helical chains. For plutonium, Pu(PDA)2 (3) was the only product isolated regardless of the Pu/ligand ratio employed in the reaction. During the reaction of plutonium with PDAH2, Pu(III) is oxidized to Pu(IV), generating 3. This assignment is consistent with structural metrics and the optical absorption spectrum. Ambiguity in the assignment of the oxidation state of cerium in 1 and 2 from UV-vis-near-IR spectra invoked the use of Ce L3,2-edge X-ray absorption near-edge spectroscopy, magnetic susceptibility, and heat capacity measurements. These experiments support the assignment of Ce(III) in both compounds. The bond distances and coordination numbers are also consistent with these assignments. 3 contains 8-coordinate Pu(IV), whereas the cerium centers in 1 and 2 are 9- and/or 10-coordinate, which correlates with the increased size of Ce(III) versus Pu(IV). Taken together, these data provide an example of a system where the differences in the redox behavior between these f elements creates more complex chemistry with cerium than with plutonium. PMID:27070401

  18. Fungus mediated synthesis of biomedically important cerium oxide nanoparticles

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • First time biological synthesis of cerium oxide oxide nanoparticles using fungus Humicola sp. • Complete characterization of cerium oxide nanoparticles. • Biosynthesis of naturally protein capped, luminescent and water dispersible CeO2 nanoparticles. • Biosynthesized CeO2 nanoparticles can be used for many biomedical applications. - Abstract: Nanomaterials can be synthesized by chemical, physical and the more recently discovered biological routes. The biological routes are advantageous over the chemical and physical ones as unlike these, the biological synthesis protocols occur at ambient conditions, are cheap, non-toxic and eco-friendly. Although purely biological and bioinspired methods for the synthesis of nanomaterials are environmentally benign and energy conserving processes, their true potential has not been explored yet and attempts are being made to extend the formation of technologically important nanoparticles using microorganisms like fungi. Though there have been reports on the biosynthesis of oxide nanoparticles by our group in the past, no attempts have been made to employ fungi for the synthesis of nanoparticles of rare earth metals or lanthanides. Here we report for the first time, the bio-inspired synthesis of biomedically important cerium oxide (CeO2) nanoparticles using the thermophilic fungus Humicola sp. The fungus Humicola sp. when exposed to aqueous solutions of oxide precursor cerium (III) nitrate hexahydrate (CeN3O9·6H2O) results in the extracellular formation of CeO2 nanoparticles containing Ce (III) and Ce (IV) mixed oxidation states, confirmed by X-ray Photoemission Spectroscopy (XPS). The formed nanoparticles are naturally capped by proteins secreted by the fungus and thus do not agglomerate, are highly stable, water dispersible and are highly fluorescent as well. The biosynthesized nanoparticles were characterized by UV–vis spectroscopy, Photoluminescence spectroscopy (PL), Transmission

  19. Structural relationships in complex hydrides of the late transition metals

    International Nuclear Information System (INIS)

    Literature data on complex hydrides of the late transition metals (groups 7-10), such as the hydrogen storage material Mg2NiH4, are reviewed with respect to order-disorder phase transitions and structural relationships. They are analysed in terms of crystallographic group-subgroup trees and their use in understanding the different crystal structures from a symmetry point of view is demonstrated. New data are presented on the low temperature behaviour of magnesium iridium hydrides and strontium rhodium hydrides studied by powder X-ray diffraction. (orig.)

  20. Technical and economic aspects of hydrogen storage in metal hydrides

    Science.gov (United States)

    Schmitt, R.

    1981-01-01

    The recovery of hydrogen from such metal hydrides as LiH, MgH2, TiH2, CaH2 and FeTiH compounds is studied, with the aim of evaluating the viability of the technique for the storage of hydrogen fuel. The pressure-temperature dependence of the reactions, enthalpies of formation, the kinetics of the hydrogen absorption and desorption, and the mechanical and chemical stability of the metal hydrides are taken into account in the evaluation. Economic aspects are considered. Development of portable metal hydride hydrogen storage reservoirs is also mentioned.

  1. PIE techniques for hydride reorientation test at NDC

    International Nuclear Information System (INIS)

    Dry storage of spent fuels in the interim storage facility is being planned in Japan. However, the gradual deterioration of the mechanical property of fuel cladding due to internal pressure and temperature during the storage term is known. Therefore, the integrity of stored fuel rods should be confirmed before the start of dry storage. For the last several years, NDC had a lot of experiences on the hydride reorientation test. The specimen preparation techniques on the hydride reorientation test and the mechanical testing techniques after the hydride reorientation are shown in this paper. (author)

  2. Jet formation in cerium metal to examine material strength

    International Nuclear Information System (INIS)

    Examining the evolution of material properties at extreme conditions advances our understanding of numerous high-pressure phenomena from natural events like meteorite impacts to general solid mechanics and fluid flow behavior. Recent advances in synchrotron diagnostics coupled with dynamic compression platforms have introduced new possibilities for examining in-situ, spatially resolved material response with nanosecond time resolution. In this work, we examined jet formation from a Richtmyer-Meshkov instability in cerium initially shocked into a transient, high-pressure phase, and then released to a low-pressure, higher-temperature state. Cerium's rich phase diagram allows us to study the yield stress following a shock induced solid-solid phase transition. X-ray imaging was used to obtain images of jet formation and evolution with 2–3 μm spatial resolution. From these images, an analytic method was used to estimate the post-shock yield stress, and these results were compared to continuum calculations that incorporated an experimentally validated equation-of-state (EOS) for cerium coupled with a deviatoric strength model. Reasonable agreement was observed between the calculations and the data illustrating the sensitivity of jet formation on the yield stress values. The data and analysis shown here provide insight into material strength during dynamic loading which is expected to aid in the development of strength aware multi-phase EOS required to predict the response of matter at extreme conditions

  3. Enhancing cerium and plutonium solubility by reduction in borosilicate glass

    Science.gov (United States)

    Cachia, J.-N.; Deschanels, X.; Den Auwer, C.; Pinet, O.; Phalippou, J.; Hennig, C.; Scheinost, A.

    2006-06-01

    High-level radioactive wastes produced by spent fuel reprocessing containing fission and activation products as well as actinides are incorporated in a borosilicate glass. To ensure optimum radionuclide containment, the resulting glass must be as homogeneous as possible. Microscopic heterogeneity can arise from various processes including the excess loading of an element above its solubility limit. The current actinide loading limit is 0.4 wt%. Work is in progress to assess the actinide solubility in these glasses, especially for plutonium. Initially the actinides were simulated by lanthanides and hafnium. The results show that trivalent elements (La, Gd) exhibit greater solubility than tetravalent elements (Pu, Hf). Cerium is an interesting element because its oxidation state varies from IV to III depending on the process conditions, such as the temperature and redox potential of the melt. In order to quantify the solubility increase, cerium-doped glass samples were melted under reducing conditions by adding a reducing agent. The solubility observed at 1473 K increased significantly from 0.95 to 13.00 wt%. Several reducing compounds have been tested. This paper deals with this study and the application to reduce Pu(IV) to Pu(III). The reduction state was characterized by X-ray absorption spectroscopy (XANES) for plutonium and by chemical analysis for cerium. The material homogeneity was verified by optical and scanning electron microscopy. Preliminary findings concerning the reduction of Pu-doped glasses fabricated in hot cells are also discussed.

  4. Dissolution of cerium from cerium-based conversion coatings on Al 7075-T6 in 0.1 M NaCl solutions

    International Nuclear Information System (INIS)

    Highlights: ► Dissolution of cerium from cerium-based conversion coatings (CeCCs) on Al 7075-T6. ► Immersion of CeCCs in 0.1 M NaCl showed dissolution only possible at pH ⩽ 2. ► Corrosion protection of CeCCs is not provided by dissolution of cerium species. ► CeCCs corrosion protection mechanism differ from chromate-based conversion coatings. - Abstract: Cerium-based conversion coatings (CeCCs) were immersed in 0.1 M NaCl for ∼500 h over a range of pH (2.0–5.7) to investigate the dissolution of cerium species. Dissolution was detected by UV–vis spectroscopy only in the pH 2 solution. Similar cerium concentrations were detected from the dissolution of as-deposited and phosphate post-treated CeCCs. Solubility diagrams for Ce(OH)3, Ce(OH)4, CeO2, and CePO4 showed that only Ce(OH)3 was soluble in acidic conditions. Although pKsp(CePO4) ≈ pKsp(Ce(OH)3), the dissolution of the post-treated CeCCs was slightly higher than the as-deposited CeCCs. Thus, corrosion protection of CeCCs is not provided solely by dissolution of cerium species.

  5. The developments and challenges of cerium half-cell in zinc–cerium redox flow battery for energy storage

    International Nuclear Information System (INIS)

    Zinc–cerium redox flow batteries (ZCBs) are emerging as a very promising new technology with the potential to store a large amount of energy economically and efficiently, thanking to its highest thermodynamic open-circuit cell voltage among all the currently studied aqueous redox flow batteries. However, there are numerous scientific and technical challenges that must be overcome if this alluring promise is to turn into reality, from designing the battery structure, to optimizing the electrolyte compositions and elucidating the complex chemical reactions that occur during charge and discharge. This review article is the first summary of the most significant developments and challenges of cerium half-cell and the current understanding of their chemistry. We are certain that this review will be of great interest to audience over a broad range, especially in fields of energy storage, electrochemistry, and chemical engineering

  6. Delayed hydride in zirconium based alloys

    International Nuclear Information System (INIS)

    Delayed Hydride Cracking (DHC) velocity along the axial direction of Zirconium-2.5% Nb pressure tube materials of different origins i.e. CANDU and RBMK (TMT -I), has been determined in the temperature range of 162 to 250 degree C. DHC crack growth was monitored using Direct Current Potential Drop Technique. It has been observed that the DHC velocity of both materials increases with increase in test temperature. The DHC velocity for the RBMK (TMT -I) material was found about 2 to 5 times lower than that for the CANDU materials at each temperature. In addition, the activation energy of the phenomena was calculated taking into account that DHC is a thermal activated mechanism, following an Arrhenius-type law. (author)

  7. The progress of nanocrystalline hydride electrode materials

    International Nuclear Information System (INIS)

    This paper reviews research at the Institute of Materials Science and Engineering, Poznan University of Technology, on the synthesis of nanocrystalline hydride electrode materials. Nanocrystalline materials have been synthesized by mechanical alloying (MA) followed by annealing. Examples of the materials include TiFe-, ZrV2-, LaNi5 and Mg2Ni-type phases. Details on the process used and the enhancement of properties due to the nanoscale structures are presented. The synthesized alloys were used as negative electrode materials for Ni-MH battery. The properties of hydrogen host materials can be modified substantially by alloying to obtain the desired storage characteristics. For example, it was found that the respective replacement of Fe in TiFe by Ni and/or by Cr, Co, Mo improved not only the discharge capacity but also the cycle life of these electrodes. The hydrogen storage properties of nanocrystalline ZrV2- and LaNi5-type powders prepared by mechanical alloying and annealing show no big difference with those of melt casting (polycrystalline) alloys. On the other hand, a partial substitution of Mg by Mn or Al in Mg2Ni alloy leads to an increase in discharge capacity, at room temperature. Furthermore, the effect of the nickel and graphite coating on the structure of some nanocrystalline alloys and the electrodes characteristics were investigated. In the case of Mg2Ni-type alloy mechanical coating with graphite effectively reduced the degradation rate of the studied electrode materials. The combination of a nanocrystalline TiFe-, ZrV2- and LaNi5-type hydride electrodes and a nickel positive electrode to form a Ni-MH battery, has been successful. (authors)

  8. Hydrogen storage in sodium aluminum hydride.

    Energy Technology Data Exchange (ETDEWEB)

    Ozolins, Vidvuds; Herberg, J.L. (Lawrence Livermore National Laboratories, Livermore, CA); McCarty, Kevin F.; Maxwell, Robert S. (Lawrence Livermore National Laboratories, Livermore, CA); Stumpf, Roland Rudolph; Majzoub, Eric H.

    2005-11-01

    Sodium aluminum hydride, NaAlH{sub 4}, has been studied for use as a hydrogen storage material. The effect of Ti, as a few mol. % dopant in the system to increase kinetics of hydrogen sorption, is studied with respect to changes in lattice structure of the crystal. No Ti substitution is found in the crystal lattice. Electronic structure calculations indicate that the NaAlH{sub 4} and Na{sub 3}AlH{sub 6} structures are complex-ionic hydrides with Na{sup +} cations and AlH{sub 4}{sup -} and AlH{sub 6}{sup 3-} anions, respectively. Compound formation studies indicate the primary Ti-compound formed when doping the material at 33 at. % is TiAl{sub 3} , and likely Ti-Al compounds at lower doping rates. A general study of sorption kinetics of NaAlH{sub 4}, when doped with a variety of Ti-halide compounds, indicates a uniform response with the kinetics similar for all dopants. NMR multiple quantum studies of solution-doped samples indicate solvent interaction with the doped alanate. Raman spectroscopy was used to study the lattice dynamics of NaAlH{sub 4}, and illustrated the molecular ionic nature of the lattice as a separation of vibrational modes between the AlH{sub 4}{sup -} anion-modes and lattice-modes. In-situ Raman measurements indicate a stable AlH{sub 4}{sup -} anion that is stable at the melting temperature of NaAlH{sub 4}, indicating that Ti-dopants must affect the Al-H bond strength.

  9. Induction of pulmonary fibrosis by cerium oxide nanoparticles

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Jane Y., E-mail: jym1@cdc.gov [Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV 26505 (United States); Mercer, Robert R.; Barger, Mark; Schwegler-Berry, Diane; Scabilloni, James [Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV 26505 (United States); Ma, Joseph K. [School of Pharmacy, West Virginia University, Morgantown, WV 26506 (United States); Castranova, Vincent [Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV 26505 (United States)

    2012-08-01

    Cerium compounds have been used as a diesel engine catalyst to lower the mass of diesel exhaust particles, but are emitted as cerium oxide (CeO{sub 2}) nanoparticles in the diesel exhaust. In a previous study, we have demonstrated a wide range of CeO{sub 2}-induced lung responses including sustained pulmonary inflammation and cellular signaling that could lead to pulmonary fibrosis. In this study, we investigated the fibrogenic responses induced by CeO{sub 2} in a rat model at various time points up to 84 days post-exposure. Male Sprague Dawley rats were exposed to CeO{sub 2} by a single intratracheal instillation. Alveolar macrophages (AM) were isolated by bronchial alveolar lavage (BAL). AM-mediated cellular responses, osteopontin (OPN) and transform growth factor (TGF)-β1 in the fibrotic process were investigated. The results showed that CeO{sub 2} exposure significantly increased fibrotic cytokine TGF-β1 and OPN production by AM above controls. The collagen degradation enzymes, matrix metalloproteinase (MMP)-2 and -9 and the tissue inhibitor of MMP were markedly increased in the BAL fluid at 1 day- and subsequently declined at 28 days after exposure, but remained much higher than the controls. CeO{sub 2} induced elevated phospholipids in BAL fluid and increased hydroxyproline content in lung tissue in a dose- and time-dependent manner. Immunohistochemical analysis showed MMP-2, MMP-9 and MMP-10 expressions in fibrotic regions. Morphological analysis noted increased collagen fibers in the lungs exposed to a single dose of 3.5 mg/kg CeO{sub 2} and euthanized at 28 days post-exposure. Collectively, our studies show that CeO{sub 2} induced fibrotic lung injury in rats, suggesting it may cause potential health effects. -- Highlights: ► Cerium oxide exposure significantly affected the following parameters in the lung. ► Induced fibrotic cytokine OPN and TGF-β1 production and phospholipidosis. ► Caused imbalance of the MMP-9/ TIMP-1 ratio that favors fibrosis

  10. Induction of pulmonary fibrosis by cerium oxide nanoparticles

    International Nuclear Information System (INIS)

    Cerium compounds have been used as a diesel engine catalyst to lower the mass of diesel exhaust particles, but are emitted as cerium oxide (CeO2) nanoparticles in the diesel exhaust. In a previous study, we have demonstrated a wide range of CeO2-induced lung responses including sustained pulmonary inflammation and cellular signaling that could lead to pulmonary fibrosis. In this study, we investigated the fibrogenic responses induced by CeO2 in a rat model at various time points up to 84 days post-exposure. Male Sprague Dawley rats were exposed to CeO2 by a single intratracheal instillation. Alveolar macrophages (AM) were isolated by bronchial alveolar lavage (BAL). AM-mediated cellular responses, osteopontin (OPN) and transform growth factor (TGF)-β1 in the fibrotic process were investigated. The results showed that CeO2 exposure significantly increased fibrotic cytokine TGF-β1 and OPN production by AM above controls. The collagen degradation enzymes, matrix metalloproteinase (MMP)-2 and -9 and the tissue inhibitor of MMP were markedly increased in the BAL fluid at 1 day- and subsequently declined at 28 days after exposure, but remained much higher than the controls. CeO2 induced elevated phospholipids in BAL fluid and increased hydroxyproline content in lung tissue in a dose- and time-dependent manner. Immunohistochemical analysis showed MMP-2, MMP-9 and MMP-10 expressions in fibrotic regions. Morphological analysis noted increased collagen fibers in the lungs exposed to a single dose of 3.5 mg/kg CeO2 and euthanized at 28 days post-exposure. Collectively, our studies show that CeO2 induced fibrotic lung injury in rats, suggesting it may cause potential health effects. -- Highlights: ► Cerium oxide exposure significantly affected the following parameters in the lung. ► Induced fibrotic cytokine OPN and TGF-β1 production and phospholipidosis. ► Caused imbalance of the MMP-9/ TIMP-1 ratio that favors fibrosis. ► Cerium oxide particles were detected in

  11. Electrochemical behavior of carbon paper on cerium methanesulfonate electrolytes for zinc-cerium flow battery

    International Nuclear Information System (INIS)

    The voltammetric behavior of the Ce(III)/(IV) half-cell reaction in various electrolytes containing 0.6 M Ce was investigated on both pristine and metal-modified carbon paper (CP) electrodes at three different temperatures (25, 40 and 55 °C) in order to find the most favorable electrochemical conditions. The pristine CP displayed robust electrochemical performance for up to 200 repetitive CV cycles while the Pt loaded electrode’s performance was stable for only 70 cycles, even though the latter exhibited a more reversible behavior, moving from a quasi-reversible to a reversible system (Dox. = 4.0 × 10−6 cm2 s−1 and Dred. = 2.5 × 10−6 cm2 s−1). The In and La metal modified electrodes did not show any improvement with regard to the kinetics or reversibility of the reaction. The addition of 1 M H2SO4 to the base electrolyte enhanced the cerium reduction reaction by a factor of 3, (−7.2 × 10−3 A cm−2). The highest exchange current densities (jo) were achieved at 40 °C for the CP-Pt (1 × 10−3 A cm−2) attributable to the presence of the catalytic Pt. Elevated temperatures (40 and 55 °C) improved D and ΔEp. while also the mass transport parameters a) dynamic viscosity (∼1.5 mPa·s) and b) electrolytic conductivity (∼265 mS cm−1) of the Ce(III)/(IV) half-cell reaction. Overall, pristine CP and to a lesser extent CP-Pt demonstrated good stability with prolonged cycling and kinetics comparable with the ones of Pt and Pt based electrodes

  12. Artificial exomuscle investigations for applications-metal hydride

    International Nuclear Information System (INIS)

    In pursuing the development of bionic devices, Victhom identified a need for technologies that could replace current motorized systems and be better integrated into the human body motion. The actuators used to obtain large displacements are noisy, heavy, and do not adequately reproduce human muscle behavior. Subsequently, a project at Victhom was devoted to the development of active materials to obtain an artificial exomuscle actuator. An exhaustive literature review was done at Victhom to identify promising active materials for the development of artificial muscles. According to this review, metal hydrides were identified as a promising technology for artificial muscle development. Victhom's investigations focused on determining metal hydride actuator potential in the context of bionics technology. Based on metal hydride properties and artificial muscle requirements such as force, displacement and rise time, an exomuscle was built. In addition, a finite element model, including heat and mass transfer in the metal hydride, was developed and implemented in FEMLAB software. (review article)

  13. Artificial exomuscle investigations for applications-metal hydride

    Energy Technology Data Exchange (ETDEWEB)

    Crevier, Marie-Charlotte; Richard, Martin; Rittenhouse, D Matheson; Roy, Pierre-Olivier; Bedard, Stephane [Victhom Human Bionics Inc., Saint-Augustin-de-Desmaures, QC (Canada)

    2007-03-01

    In pursuing the development of bionic devices, Victhom identified a need for technologies that could replace current motorized systems and be better integrated into the human body motion. The actuators used to obtain large displacements are noisy, heavy, and do not adequately reproduce human muscle behavior. Subsequently, a project at Victhom was devoted to the development of active materials to obtain an artificial exomuscle actuator. An exhaustive literature review was done at Victhom to identify promising active materials for the development of artificial muscles. According to this review, metal hydrides were identified as a promising technology for artificial muscle development. Victhom's investigations focused on determining metal hydride actuator potential in the context of bionics technology. Based on metal hydride properties and artificial muscle requirements such as force, displacement and rise time, an exomuscle was built. In addition, a finite element model, including heat and mass transfer in the metal hydride, was developed and implemented in FEMLAB software. (review article)

  14. Formation of hydride blisters in zirconium alloy pressure tubes

    International Nuclear Information System (INIS)

    The fracture of the Zircaloy-2 pressure tube in the Pickering Unit 2 power reactor was associated with the growth of hydride blisters at points of contact between the pressure tube and the cooler calandria tube surrounding it. Similar blisters have been observed in a Zr-2.5 wt% Nb pressure tube in WR-1, an organic-cooled research reactor. These hydride blisters were formed and grew as a result of the thermal diffusion of hydrogen in the zirconium, a mechanism whereby hydrogen diffuses down a temperature gradient. If the terminal solid solubility of hydrogen is exceeded in the cooler regions, hydride will precipitate. In this paper, the time required to grow these hydride blisters will be estimated from the blister size and the hydrogen distribution in its neighborhood, by using simple equations derived from thermal diffusion theory

  15. Out-of-pile accelerated hydriding of Zircaloy fasteners

    International Nuclear Information System (INIS)

    Mechanical joints between Zircaloy and nickel-bearing alloys, mainly the Zircaloy-4/Inconel-600 combination, were exposed to water at 4500F and 5200F to study hydriding of Zircaloy in contact with a dissimilar metal. Accelerated hydriding of the Zircaloy occurred at both temperatures. At 4500F the dissolved hydrogen level of the water was over ten times that at 5200F. At 5200F the initially high hydrogen ingress rate decreased rapidly as exposure time increased and was effectively shut off in about 25 days. Severely hydrided Zircaloy components successfully withstood thermal cycling and mechanical testing. Chromium plating of the nickel-bearing parts was found to be an effective and practical barrier in preventing nickel-alloy smearing and accelerated hydriding of Zircaloy

  16. A nuclear analytical model for uranium zirconium hydride reactor core

    International Nuclear Information System (INIS)

    The nuclear analytical model and codes for the uranium zirconium hydride reactor are outlined. The criticality and control rods effeciency of abroad TRIGA reactor are obtained using this model and codes. The results are satisfactory

  17. A mechanistic approach to develop the secondary hydriding criteria

    International Nuclear Information System (INIS)

    Reliable criteria of secondary hydriding failures are important to assure safe operation of nuclear fuel in LWR power units. The present paper reviews available data on massive hydriding of Zirconium claddings covering out-of-pile studies and in-pile tests in research reactors. Analyses of these experimental data give evidence that threshold conditions leading to the onset of massive hydriding are drastically changed under irradiation. The changes are caused mainly by irradiation damage of oxygen sublattice in ZrO2 by fission fragments leaving the periphery of fuel pellets. The tests in research reactors provide a basis to develop a parametric dependency which relates the threshold of massive hydriding to composition of steam-hydrogen mixture, irradiation dose rate and temperature

  18. Transparent yttrium hydride thin films prepared by reactive sputtering

    OpenAIRE

    Mongstad, T.; Platzer-Björkman, C.; Karazhanov, S. Zh.; Holt, A.; Maehlen, J. P.; Hauback, B. C.

    2011-01-01

    Metal hydrides have earlier been suggested for utilization in solar cells. With this as a motivation we have prepared thin films of yttrium hydride by reactive magnetron sputter deposition. The resulting films are metallic for low partial pressure of hydrogen during the deposition, and black or yellow-transparent for higher partial pressure of hydrogen. Both metallic and semiconducting transparent YHx films have been prepared directly in-situ without the need of capping layers and post-deposi...

  19. The Production of Uranium Metal by Metal Hydrides Incorporated

    Energy Technology Data Exchange (ETDEWEB)

    Alexander, P. P.

    1943-01-01

    Metal Hydrides Incorporated was a pioneer in the production of uranium metal on a commercial scale and supplied it to all the laboratories interested in the original research, before other methods for its production were developed. Metal Hydrides Inc. supplied the major part of the metal for the construction of the first experimental pile which, on December 2, 1942, demonstrated the feasibility of the self-sustaining chain reaction and the release of atomic energy.

  20. Electronic structure and optical properties of lightweight metal hydrides

    NARCIS (Netherlands)

    Setten, van M.J.; Popa, V.A.; Wijs, de G.A.; Brocks, G.

    2007-01-01

    We study the dielectric functions of the series of simple hydrides LiH, NaH, MgH2, and AlH3, and of the complex hydrides Li3AlH6, Na3AlH6, LiAlH4, NaAlH4, and Mg(AlH4)2, using first-principles density-functional theory and GW calculations. All compounds are large gap insulators with GW single-partic

  1. Thin-film metal hydrides for solar energy applications

    OpenAIRE

    2012-01-01

    Thin-film metal hydrides may become important solar energy materials in the future. This thesis demonstrates interesting material properties of metal hydride films, relevant for applications as semiconducting materials for photovoltaic (PV) solar cells and for regulation of light using smart window technology. List of papers. Papers II-VI are removed from the thesis due to copyright restrictions. Paper I C. Platzer-Björkman, T. Mongstad, S. Zh. Karazhanov, J. P. Mæhlen, E. S. Marst...

  2. Suppression of the critical temperature in binary vanadium hydrides

    International Nuclear Information System (INIS)

    Highlights: • Addition of 10 mol% Cr to V increases the β-hydride TC to >200 °C. • Addition of 10 mol% Ni to V increases the β-hydride TC to >400 °C. • Addition of 10 mol% Al to V decreases the β-hydride TC to 90Al10 membrane can be cycled to 2 without β-hydride formation. -- Abstract: The tendency of vanadium-based alloy membranes to embrittle is the biggest commercialisation barrier for this hydrogen separation technology. Excessive hydrogen absorption and the α → β hydride transition both contribute to brittle failure of these membranes. Alloying is known to reduce absorption, but the influence of alloying on hydride phase formation under conditions relevant to membrane operation has not been studied in great detail previously. Here, the effect of Cr, Ni, and Al alloying additions on V–H phase equilibrium has been studied using hydrogen absorption measurements and in situ X-ray diffraction studies. The addition of 10 mol% Ni increases the critical temperature for α + β hydride formation to greater than 400 °C, compared to 170 °C for V. Cr also increases the critical temperature, to between 200 and 300 °C. The addition of 10 mol% Al, however, suppresses the critical temperature to less than 30 °C, thereby enabling this material to be cycled thermally and hydrostatically while precluding formation of the β-hydride phase. This is despite Al also decreasing hydrogen absorption. The implication of this finding is that one of the mechanisms of brittle failure in vanadium-based hydrogen-selective membranes has been eliminated, thereby increasing the robustness of this material relative to V

  3. Modelling of fuel rod hydriding failures in water reactors

    International Nuclear Information System (INIS)

    Mechanistic models which were developed to describe primary hydriding phenomena in claddings of initially intact rods with residual moisture are described. The models include the following key processes: fuel rod thermal behavior, UO2 fuel oxidation in steam-hydrogen atmosphere under irradiation, hydrogen diffusion in zirconium and in the hydride, growth of the hydride phase. Fuel rod thermomechanical behavior is calculated by using RTOP integral fuel code. An oxidation model represents the effects of temperature dynamics and temperature profile along fuel axis and radius on fuel oxidation as well as on hydrogen accumulation inside the fuel rod. Along with ordinary thermal dissociation of water molecules, the oxidation model also addresses radiolysis of the steam-hydrogen mixture due to fission fragments. The present radiolysis model takes into account the effects of the gas mixture composition, temperature and pressure. A new model of cladding hydriding is proposed in which calculation of the massive hydride growth is performed in 2-D geometry. Hydrogen transport in zirconium cladding is modeled with account for thermodiffusion. The RTOP code comprising the models developed allows us to calculate different scenarios of hydriding rod failures under given operation conditions. Test calculations were carried out and compared to available data. It is shown that there are threshold values of initial steam content inside the intact fuel rod which lead to the possibility of through-cladding hydride growth and formation of the primary defect. The threshold values depend on the oxidation state of the cladding inner surface, linear power profile in the fuel rod, fuel rod geometry, cladding temperature conditions and hydrogen diffusivities in zirconium and zirconium hydride

  4. Hydride distribution around a blister in Zr-2.5Nb pressure tubes

    International Nuclear Information System (INIS)

    Blisters were grown in Zr-2.5Nb pressure tube sections by a thermal gradient without applying external stress. The surrounding hydride distribution was analyzed. Hydride platelets were observed in the radial direction of the blister. The precipitation of these hydrides was found to be favored by low temperature of blister growth and slow cooling rate after blister formation. The misfit strain produced by hydride blister growth provides the stress necessary to promote radial precipitation. During the subsequent tensile test at 200 C (delayed hydride cracking test) the radial hydride length and thickness are increased. This increase is explained by a stress concentrator effect of the blister. When this effect vanishes, the increase of radial hydrides continues by an autocatalytic effect and stress concentrator effect of the hydride platelet. If a crack originated in the blister reaches the matrix it could propagate along a radial hydride previously precipitated. (orig.)

  5. Optimization of Hydride Rim Formation in Unirradiated Zr 4 Cladding

    Energy Technology Data Exchange (ETDEWEB)

    Shimskey, Rick W.; Hanson, Brady D.; MacFarlan, Paul J.

    2013-09-30

    The purpose of this work is to build on the results reported in the M2 milestone M2FT 13PN0805051, document number FCRD-USED-2013-000151 (Hanson, 2013). In that work, it was demonstrated that unirradiated samples of zircaloy-4 cladding could be pre-hydrided at temperatures below 400°C in pure hydrogen gas and that the growth of hydrides on the surface could be controlled by changing the surface condition of the samples and form a desired hydride rim on the outside diameter of the cladding. The work performed at Pacific Northwest National Laboratory since the issuing of the M2 milestone has focused its efforts to optimize the formation of a hydride rim on available zircaloy-4 cladding samples by controlling temperature variation and gas flow control during pre-hydriding treatments. Surface conditioning of the outside surface was also examined as a variable. The results of test indicate that much of the variability in the hydride thickness is due to temperature variation occurring in the furnaces as well as how hydrogen gas flows across the sample surface. Efforts to examine other alloys, gas concentrations, and different surface conditioning plan to be pursed in the next FY as more cladding samples become available

  6. Metal Hydrides for High-Temperature Power Generation

    Directory of Open Access Journals (Sweden)

    Ewa C. E. Rönnebro

    2015-08-01

    Full Text Available Metal hydrides can be utilized for hydrogen storage and for thermal energy storage (TES applications. By using TES with solar technologies, heat can be stored from sun energy to be used later, which enables continuous power generation. We are developing a TES technology based on a dual-bed metal hydride system, which has a high-temperature (HT metal hydride operating reversibly at 600–800 °C to generate heat, as well as a low-temperature (LT hydride near room temperature that is used for hydrogen storage during sun hours until there is the need to produce electricity, such as during night time, a cloudy day or during peak hours. We proceeded from selecting a high-energy density HT-hydride based on performance characterization on gram-sized samples scaled up to kilogram quantities with retained performance. COMSOL Multiphysics was used to make performance predictions for cylindrical hydride beds with varying diameters and thermal conductivities. Based on experimental and modeling results, a ~200-kWh/m3 bench-scale prototype was designed and fabricated, and we demonstrated the ability to meet or exceed all performance targets.

  7. Metal hydrides based high energy density thermal battery

    Energy Technology Data Exchange (ETDEWEB)

    Fang, Zhigang Zak, E-mail: zak.fang@utah.edu [Department of Metallurgical Engineering, The University of Utah, 135 South 1460 East, Room 412, Salt Lake City, UT 84112-0114 (United States); Zhou, Chengshang; Fan, Peng [Department of Metallurgical Engineering, The University of Utah, 135 South 1460 East, Room 412, Salt Lake City, UT 84112-0114 (United States); Udell, Kent S. [Department of Metallurgical Engineering, The University of Utah, 50 S. Central Campus Dr., Room 2110, Salt Lake City, UT 84112-0114 (United States); Bowman, Robert C. [Department of Metallurgical Engineering, The University of Utah, 135 South 1460 East, Room 412, Salt Lake City, UT 84112-0114 (United States); Vajo, John J.; Purewal, Justin J. [HRL Laboratories, LLC, 3011 Malibu Canyon Road, Malibu, CA 90265 (United States); Kekelia, Bidzina [Department of Metallurgical Engineering, The University of Utah, 50 S. Central Campus Dr., Room 2110, Salt Lake City, UT 84112-0114 (United States)

    2015-10-05

    Highlights: • The principle of the thermal battery using advanced metal hydrides was demonstrated. • The thermal battery used MgH{sub 2} and TiMnV as a working pair. • High energy density can be achieved by the use of MgH{sub 2} to store thermal energy. - Abstract: A concept of thermal battery based on advanced metal hydrides was studied for heating and cooling of cabins in electric vehicles. The system utilized a pair of thermodynamically matched metal hydrides as energy storage media. The pair of hydrides that was identified and developed was: (1) catalyzed MgH{sub 2} as the high temperature hydride material, due to its high energy density and enhanced kinetics; and (2) TiV{sub 0.62}Mn{sub 1.5} alloy as the matching low temperature hydride. Further, a proof-of-concept prototype was built and tested, demonstrating the potential of the system as HVAC for transportation vehicles.

  8. Direct growth of cerium oxide nanorods on diverse substrates for superhydrophobicity and corrosion resistance

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Cerium oxide nanorods were uniformly grown on diverse substrates. • Changes in growth conditions led to morphology evolution of cerium oxide nanostructures. • The grown cerium oxide nanostructures were single or poly crystalline. • Direct growth of cerium oxide nanorods made the diverse substrates superhydrophobic and anti-corrosive without any surface modifiers. - Abstract: Superhydrophobic surfaces with anti-corrosion properties have attracted great interest in many industrial fields, particularly to enhance the thermal performance of offshore applications such as heat exchangers, pipelines, power plants, and platform structures. Nanostructures with hydrophobic materials have been widely utilized to realize superhydrophobicity of surfaces, and cerium oxide has been highlighted due to its good corrosion resistive and intrinsically hydrophobic properties. However, few studies of direct growth of cerium oxide nanostructures on diverse substrates have been reported. Herein we report a facile hydrothermal method to directly grow cerium oxide nanorods on diverse substrates, such as aluminum alloy, stainless steel, titanium, and silicon. Diverse substrates with cerium oxide nanorods exhibited superhydrophobicity with no hydrophobic modifiers on their surfaces, and showed good corrosion resistive properties in corrosive medium. We believe our method could pave the way for realization of scalable and sustainable corrosion resistive superhydrophobic surfaces in many industrial fields

  9. EIS study of nano crystalline Ni-cerium oxide coating electrodeposition mechanism

    Energy Technology Data Exchange (ETDEWEB)

    Hasannejad, H. [Department of Materials Science and Engineering, Tarbiat Modares University, Tehran (Iran, Islamic Republic of); Shahrabi, T., E-mail: Tshahrabi34@modares.ac.ir [Department of Materials Science and Engineering, Tarbiat Modares University, Tehran (Iran, Islamic Republic of); Jafarian, M. [Department of Chemistry, K.N. Toosi University of Technology, P.O. Box 15875-4416, Tehran (Iran, Islamic Republic of); Rouhaghdam, A. Sabour [Department of Materials Science and Engineering, Tarbiat Modares University, Tehran (Iran, Islamic Republic of)

    2011-02-03

    Research highlights: > In this study a new procedure was used for electrodeposition of Ni-cerium oxide amorphous-nano crystalline composite coatings. The innovation of this method is that the metal and oxides are deposited simultaneously on the samples from the plating bath solution containing Ni ions and Ce ions with no powder added. - Abstract: In this study a novel procedure was used for the electrodeposition of Ni-cerium oxide nano crystalline composite coatings. The novelty of this method lies in the fact that the metal and the oxide are both deposited simultaneously on the substrate, directly from the plating bath containing Ni and Ce ions with no oxide powder addition. Electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), X-ray diffraction (XRD) and energy dispersive spectroscopy (EDS) were used to study the mechanisms of Ni-CeO{sub 2} nanocomposite coating deposition. The results indicated that the morphology of Ni-cerium oxide coatings varied based on the Ni:Ce ion ratio. When this ratio exceeds 100, sporadic distribution of cerium oxide in the Ni matrix occurred. On the other hand, when the aforementioned ratio was less than 100, it was found that Ni species were dispersed in a continuous film of cerium oxide. Furthermore, it was observed that Ni in Ni-cerium oxide composite coating was nanocrystalline, while cerium oxide was amorphous. Introduction of the cerium ions to the plating bath resulted in the reduction of the Ni grains average size.

  10. Electrodeposition of cerium from fused mixture of CeCl sub(3)+NaCl-KCl

    International Nuclear Information System (INIS)

    Metallic cerium has been prepared by fused salt electrolysis of 30% CeCl sub(3)+ NaCl-KCl (equimolar) mixture, in the temperature ranged 650-850 sup(0)C, in argon atmosphere. The metal nodules were collected from solidified salts bath. Analysis of these nodules has been done and a 97,3% metallic cerium was obtained. (author)

  11. EIS study of nano crystalline Ni-cerium oxide coating electrodeposition mechanism

    International Nuclear Information System (INIS)

    Research highlights: → In this study a new procedure was used for electrodeposition of Ni-cerium oxide amorphous-nano crystalline composite coatings. The innovation of this method is that the metal and oxides are deposited simultaneously on the samples from the plating bath solution containing Ni ions and Ce ions with no powder added. - Abstract: In this study a novel procedure was used for the electrodeposition of Ni-cerium oxide nano crystalline composite coatings. The novelty of this method lies in the fact that the metal and the oxide are both deposited simultaneously on the substrate, directly from the plating bath containing Ni and Ce ions with no oxide powder addition. Electrochemical impedance spectroscopy (EIS), scanning electron microscopy (SEM), X-ray diffraction (XRD) and energy dispersive spectroscopy (EDS) were used to study the mechanisms of Ni-CeO2 nanocomposite coating deposition. The results indicated that the morphology of Ni-cerium oxide coatings varied based on the Ni:Ce ion ratio. When this ratio exceeds 100, sporadic distribution of cerium oxide in the Ni matrix occurred. On the other hand, when the aforementioned ratio was less than 100, it was found that Ni species were dispersed in a continuous film of cerium oxide. Furthermore, it was observed that Ni in Ni-cerium oxide composite coating was nanocrystalline, while cerium oxide was amorphous. Introduction of the cerium ions to the plating bath resulted in the reduction of the Ni grains average size.

  12. Direct growth of cerium oxide nanorods on diverse substrates for superhydrophobicity and corrosion resistance

    Energy Technology Data Exchange (ETDEWEB)

    Cho, Young Jun; Jang, Hanmin; Lee, Kwan-Soo [School of Mechanical Engineering, Hanyang University, Seoul 133-791 (Korea, Republic of); Kim, Dong Rip, E-mail: dongrip@hanyang.ac.kr [School of Mechanical Engineering, Hanyang University, Seoul 133-791 (Korea, Republic of); Institute of Nano Science and Technology, Hanyang University, Seoul 133-791 (Korea, Republic of)

    2015-06-15

    Graphical abstract: - Highlights: • Cerium oxide nanorods were uniformly grown on diverse substrates. • Changes in growth conditions led to morphology evolution of cerium oxide nanostructures. • The grown cerium oxide nanostructures were single or poly crystalline. • Direct growth of cerium oxide nanorods made the diverse substrates superhydrophobic and anti-corrosive without any surface modifiers. - Abstract: Superhydrophobic surfaces with anti-corrosion properties have attracted great interest in many industrial fields, particularly to enhance the thermal performance of offshore applications such as heat exchangers, pipelines, power plants, and platform structures. Nanostructures with hydrophobic materials have been widely utilized to realize superhydrophobicity of surfaces, and cerium oxide has been highlighted due to its good corrosion resistive and intrinsically hydrophobic properties. However, few studies of direct growth of cerium oxide nanostructures on diverse substrates have been reported. Herein we report a facile hydrothermal method to directly grow cerium oxide nanorods on diverse substrates, such as aluminum alloy, stainless steel, titanium, and silicon. Diverse substrates with cerium oxide nanorods exhibited superhydrophobicity with no hydrophobic modifiers on their surfaces, and showed good corrosion resistive properties in corrosive medium. We believe our method could pave the way for realization of scalable and sustainable corrosion resistive superhydrophobic surfaces in many industrial fields.

  13. Cerium doped red mud catalytic ozonation for bezafibrate degradation in wastewater: Efficiency, intermediates, and toxicity.

    Science.gov (United States)

    Xu, Bingbing; Qi, Fei; Sun, Dezhi; Chen, Zhonglin; Robert, Didier

    2016-03-01

    In this study, the performance of bezafibrate (BZF) degradation and detoxification in the aqueous phase using cerium-modified red mud (RM) catalysts prepared using different cerium sources and synthesis methods were evaluated. Experimental results showed that the surface cerium modification was responsible for the development of the catalytic activity of RM and this was influenced by the cerium source and the synthesis method. Catalyst prepared from cerium (IV) by precipitation was found to show the best catalytic activity in BZF degradation and detoxification. Reactive oxygen species including peroxides, hydroxyl radicals, and super oxide ions were identified in all reactions and we proposed the corresponding catalytic reaction mechanism for each catalyst that prepared from different cerium source and method. This was supported by the intermediates profiles that were generated upon BZF degradation. The surface and the structural properties of cerium-modified RM were characterized in detail by several analytical methods. Two interesting findings were made: (1) the surface texture (specific surface area and mesoporous volume) influenced the catalytic reaction pathway; and (2) Ce(III) species and oxygen vacancies were generated on the surface of the catalyst after cerium modification. This plays an important role in the development of the catalytic activity. PMID:26706928

  14. U-8 wt %Mo and 7 wt %Mo alloys powder obtained by an hydride-de hydride process

    International Nuclear Information System (INIS)

    Uranium-molybdenum alloys are been tested as a component in high-density LEU dispersion fuels with very good performances. These alloys need to be transformed to powder due to the manufacturing requirements of the fuels. One method to convert ductile alloys into powder is the hydride-de hydride process, which takes advantage of the ability of the U-α phase to transform to UH3: a brittle and relatively low-density compound. U-Mo alloys around 7 and 8 wt % Mo were melted and heat treated at different temperature ranges in order to partially convert γ -phase to α -phase. Subsequent hydriding transforms this α -phase to UH3. The volume change associated to the hydride formation embrittled the material which ends up in a powdered alloy. Results of the optical metallography, scanning electron microscopy, X-ray diffraction during different steps of the process are shown. (author)

  15. Tuning Reactivity and Electronic Properties through Ligand Reorganization within a Cerium Heterobimetallic Framework

    Energy Technology Data Exchange (ETDEWEB)

    Robinson, Jerome R.; Gordon, Zachary; Booth, Corwin H.; Carroll, Patrick J.; Walsh, Patrick J.; Schelter, Eric J.

    2014-06-24

    Cerium compounds have played vital roles in organic, inorganic, and materials chemistry due to their reversible redox chemistry between trivalent and tetravalent oxidation states. However, attempts to rationally access molecular cerium complexes in both oxidation states have been frustrated by unpredictable reactivity in cerium(III) oxidation chemistry. Such oxidation reactions are limited by steric saturation at the metal ion, which can result in high energy activation barriers for electron transfer. An alternative approach has been realized using a rare earth/alkali metal/1,1'-BINOLate (REMB) heterobimetallic framework, which uses redox-inactive metals within the secondary coordination sphere to control ligand reorganization. The rational syntheses of functionalized cerium(IV) products and a mechanistic examination of the role of ligand reorganization in cerium(III) oxidation are presented.

  16. A quantitative phase field model for hydride precipitation in zirconium alloys: Part II. Modeling of temperature dependent hydride precipitation

    International Nuclear Information System (INIS)

    A quantitative free energy functional developed in Part I (Shi and Xiao, 2014 [1]) was applied to model temperature dependent δ-hydride precipitation in zirconium in real time and real length scale. At first, the effect of external tensile load on reorientation of δ-hydrides was calibrated against experimental observations, which provides a modification factor for the strain energy in free energy formulation. Then, two types of temperature-related problems were investigated. In the first type, the effect of temperature transient was studied by cooling the Zr–H system at different cooling rates from high temperature while an external tensile stress was maintained. At the end of temperature transients, the average hydride size as a function of cooling rate was compared to experimental data. In the second type, the effect of temperature gradients was studied in a one or two dimensional temperature field. Different boundary conditions were applied. The results show that the hydride precipitation concentrated in low temperature regions and that it eventually led to the formation of hydride blisters in zirconium. A brief discussion on how to implement the hysteresis of hydrogen solid solubility on hydride precipitation and dissolution in the developed phase field scheme is also presented

  17. Hydriding and dehydriding characteristics of LiBH4 and transition metals-added magnesium hydride

    International Nuclear Information System (INIS)

    Graphical abstract: Hydriding reaction curves under 12 bar H2, and dehydriding reaction curves under 1.0 bar H2, at 593 K at the 1st cycle for MgH2–10Ni–2LiBH4–2Ti and MgH2. Highlights: ► Addition of Ni, LiBH4, and Ti to MgH2 to increase reaction rates. ► Sample preparation by reactive mechanical grinding. ► At n = 2, the sample absorbed 4.05 wt% H for 60 min at 593 K under 12 bar H2. ► Analysis of rate-controlling step for dehydriding of the sample at n = 3. - Abstract: In this study, MgH2 was used as a starting material instead of Mg. Ni, Ti, and LiBH4 with a high hydrogen-storage capacity of 18.4 wt% were added. A sample with a composition of MgH2–10Ni–2LiBH4–2Ti was prepared by reactive mechanical grinding. The activation of MgH2–10Ni–2LiBH4–2Ti was completed after the first hydriding–dehydrding cycle. The hydriding rate decreases as the temperature increases due to the decrease in the driving force for the hydriding reaction. At the 1st cycle, the sample desorbs 1.45 wt% H for 10 min, 2.54 wt% H for 20 min, 3.13 wt% H for 30 min, and 3.40 wt% H for 60 min at 593 K under 1.0 bar H2. At the 2nd cycle, the sample absorbs 3.84 wt% H for 5 min, 3.96 wt% H for 10 min, and 4.05 wt% H for 60 min at 593 K under 12 bar H2. MgH2–10Ni–2LiBH4–2Ti after reactive mechanical grinding contained MgH2, Mg, Ni, TiH1.924, and MgO phases. The reactive mechanical grinding of Mg with Ni, LiBH4, and Ti is considered to create defects on the surface and in the interior of Mg (to facilitate nucleation), and to reduce the particle size of Mg (to shorten diffusion distances of hydrogen atoms). The formation of Mg2Ni during hydriding–dehydriding cycling increases the hydriding and dehydriding rates of the sample

  18. Chemical Hydride Slurry for Hydrogen Production and Storage

    Energy Technology Data Exchange (ETDEWEB)

    McClaine, Andrew W

    2008-09-30

    The purpose of this project was to investigate and evaluate the attractiveness of using a magnesium chemical hydride slurry as a hydrogen storage, delivery, and production medium for automobiles. To fully evaluate the potential for magnesium hydride slurry to act as a carrier of hydrogen, potential slurry compositions, potential hydrogen release techniques, and the processes (and their costs) that will be used to recycle the byproducts back to a high hydrogen content slurry were evaluated. A 75% MgH2 slurry was demonstrated, which was just short of the 76% goal. This slurry is pumpable and storable for months at a time at room temperature and pressure conditions and it has the consistency of paint. Two techniques were demonstrated for reacting the slurry with water to release hydrogen. The first technique was a continuous mixing process that was tested for several hours at a time and demonstrated operation without external heat addition. Further work will be required to reduce this design to a reliable, robust system. The second technique was a semi-continuous process. It was demonstrated on a 2 kWh scale. This system operated continuously and reliably for hours at a time, including starts and stops. This process could be readily reduced to practice for commercial applications. The processes and costs associated with recycling the byproducts of the water/slurry reaction were also evaluated. This included recovering and recycling the oils of the slurry, reforming the magnesium hydroxide and magnesium oxide byproduct to magnesium metal, hydriding the magnesium metal with hydrogen to form magnesium hydride, and preparing the slurry. We found that the SOM process, under development by Boston University, offers the lowest cost alternative for producing and recycling the slurry. Using the H2A framework, a total cost of production, delivery, and distribution of $4.50/kg of hydrogen delivered or $4.50/gge was determined. Experiments performed at Boston

  19. Simultaneous Heat and Mass Transfer in DU Hydriding

    International Nuclear Information System (INIS)

    The sources of nuclear fusion reaction are deuterium (D) and tritium (T). Generally, D is fused into T, which generates helium atoms and neutrons. At this time, a tremendous amount of energy is generated. D + T → 4He + n (E = 17.6 MeV) Hydrogen is a gas, and cannot be stored in large amounts. In addition, it can be explosive. Therefore, one of the storing methods for hydrogen is metal hydride. In this research, several kinds of metal hydrides including U, Zr, ZrCo, ZrNi, and LaNi5 have been simulated through modeling work of hydrogen absorption, desorption, and pressure effect in a bed using DU. For the exact modeling of the hydriding process, it is necessary to calculate simultaneous heat and mass transfer because, in the hydriding process, not only is hydrogen gas transported by mass transport and chemisorption but heat transfer also occurs through absorption. Therefore, in this paper, we tried to calculate the simultaneous heat and mass transfer using numerical analysis methods. Simultaneous heat and mass transfer in DU hydriding is well fitted compared to the experimental data, and is more reasonable considering only one variable. The hydriding process changes the temperature and atomic ratio simultaneously, and thus it is necessary to consider in company with two transport phenomena. The numerical analysis method applied Euler's method; however, the Runge-Kutta method is a more widely used numerical solution of a differential equation. Therefore, when analyzing the hydriding process, Runge-Kutta or another method will henceforth be applied

  20. Influence of uranium hydride oxidation on uranium metal behaviour

    International Nuclear Information System (INIS)

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

  1. The recrystallization and texture of magnesium-zinc-cerium alloys

    Energy Technology Data Exchange (ETDEWEB)

    Mackenzie, L.W.F. [Novelis Global Technology Centre, 945 Princess Street, Kingston, Ontario, K7L 5L9 (Canada); Department of Mining and Materials Engineering, McGill University, 3610 University, Montreal, Quebec, H3A 2B2 (Canada)], E-mail: luke.mackenzie@novelis.com; Pekguleryuz, M.O. [Department of Mining and Materials Engineering, McGill University, 3610 University, Montreal, Quebec, H3A 2B2 (Canada)

    2008-09-15

    Optical microscopy, electron backscatter diffraction and X-ray diffraction are employed to characterize the microstructures and textures of as-rolled and annealed Mg-1Zn and Mg-1Zn-xCe. Mg-1Zn exhibited 'basal' textures: the basal poles aligned with the sheet normal direction. With the addition of cerium, the texture was basal when recrystallization was limited; during recrystallization, the basal texture component weakened, to be replaced by a component with basal poles rotated {approx}45 deg. towards the transverse direction. Deformation, recrystallization and texture are discussed.

  2. The recrystallization and texture of magnesium-zinc-cerium alloys

    International Nuclear Information System (INIS)

    Optical microscopy, electron backscatter diffraction and X-ray diffraction are employed to characterize the microstructures and textures of as-rolled and annealed Mg-1Zn and Mg-1Zn-xCe. Mg-1Zn exhibited 'basal' textures: the basal poles aligned with the sheet normal direction. With the addition of cerium, the texture was basal when recrystallization was limited; during recrystallization, the basal texture component weakened, to be replaced by a component with basal poles rotated ∼45 deg. towards the transverse direction. Deformation, recrystallization and texture are discussed

  3. Hydriding and neutron irradiation in zircaloy-4

    International Nuclear Information System (INIS)

    The composition of Zircaloy-4 for nuclear applications is specified by the ASTM B350 Standard, that fixes the amount of alloying elements (Sn, Fe, Cr) and impurities (Ni, Hf, O, N, C, among others) to optimize good corrosion and mechanical behavior.The recycling of zircaloy-4 scrap and chips resulting from cladding tube fabrication is an interesting issue.However, changes in the final composition of the recycled material may occur due to contamination with tool pieces, stainless steel chips, turnings, etc. while scrap is stored and handled. Since the main components of the possible contaminants are Fe, Cr and Ni, it arises the interest in studying up to what limit the Fe, Ni and Cr contents could be exceeded beyond the standard specification without affecting significantly the alloy properties.Zircaloy-4 alloys elaborated with Fe, Cr and Ni additions and others of standard composition in use in nuclear plants are studied by tensile tests, SEM observations and EDS microanalysis.Some samples are tested in the initial condition and others after hydriding treatments and neutron irradiation in the RA6

  4. Reactions of NO with nitrogen hydrides x

    Science.gov (United States)

    Mebel, A. M.; Lin, M. C.

    In this review, we consider the reactions of NO ( x 1,2) with the nitrogen x hydrides NH, NH and NH . The reactions are relevant to the post-combustion, non-catalytic reduction of NO with NH in the thermal de-NO process and with x x HNCO in the rapid reduction of NO as well as to the thermal decomposition of x some high-energy materials, including ammonium dinitramide. The practical importance has motivated considerable theoretical interest in these reactions. We review numerous ab - initio molecular orbital studies of potential energy surfaces for NO NH and theoretical calculations of their kinetic parameters, such as x y thermal rate constants and branching ratios of various products. The most advanced theoretical calculations are carried out using the Gaussian-2 family of methods which provides the chemical accuracy (within 2 kcal mol ) for the energetics and molecular parameters of the reactants, products, intermediates and transition states. We present a detailed comparison of the theoretical results with available experimental data. We show that the reactions of NO with NH and NH x are very fast because they occur without a barrier and lead to the formation of multiple products which include radicals and stable molecules. The reactions of NO with NH , taking place by the H abstraction to form NH and HNO , are slow x x but still relevant to the NH de-NO system, because of their fast reverse processes x which have not yet been measured experimentally.

  5. Soil organic matter influences cerium translocation and physiological processes in kidney bean plants exposed to cerium oxide nanoparticles.

    Science.gov (United States)

    Majumdar, Sanghamitra; Peralta-Videa, Jose R; Trujillo-Reyes, Jesica; Sun, Youping; Barrios, Ana C; Niu, Genhua; Margez, Juan P Flores-; Gardea-Torresdey, Jorge L

    2016-11-01

    Soil organic matter plays a major role in determining the fate of the engineered nanomaterials (ENMs) in the soil matrix and effects on the residing plants. In this study, kidney bean plants were grown in soils varying in organic matter content and amended with 0-500mg/kg cerium oxide nanoparticles (nano-CeO2) under greenhouse condition. After 52days of exposure, cerium accumulation in tissues, plant growth and physiological parameters including photosynthetic pigments (chlorophylls and carotenoids), net photosynthesis rate, transpiration rate, and stomatal conductance were recorded. Additionally, catalase and ascorbate peroxidase activities were measured to evaluate oxidative stress in the tissues. The translocation factor of cerium in the nano-CeO2 exposed plants grown in organic matter enriched soil (OMES) was twice as the plants grown in low organic matter soil (LOMS). Although the leaf cover area increased by 65-111% with increasing nano-CeO2 concentration in LOMS, the effect on the physiological processes were inconsequential. In OMES leaves, exposure to 62.5-250mg/kg nano-CeO2 led to an enhancement in the transpiration rate and stomatal conductance, but to a simultaneous decrease in carotenoid contents by 25-28%. Chlorophyll a in the OMES leaves also decreased by 27 and 18% on exposure to 125 and 250mg/kg nano-CeO2. In addition, catalase activity increased in LOMS stems, and ascorbate peroxidase increased in OMES leaves of nano-CeO2 exposed plants, with respect to control. Thus, this study provides clear evidence that the properties of the complex soil matrix play decisive roles in determining the fate, bioavailability, and biological transport of ENMs in the environment. PMID:27343939

  6. Micro-scale fracture experiments on zirconium hydrides and phase boundaries

    Science.gov (United States)

    Chan, H.; Roberts, S. G.; Gong, J.

    2016-07-01

    Fracture properties of micro-scale zirconium hydrides and phase boundaries were studied using microcantilever testing methods. FIB-machined microcantilevers were milled on cross-sectional surfaces of hydrided samples, with the most highly-stressed regions within the δ-hydride film, within the α-Zr or along the Zr-hydride interface. Cantilevers were notched using the FIB and then tested in bending using a nanoindenter. Load-displacement results show that three types of cantilevers have distinct deformation properties. Zr cantilevers deformed plastically. Hydride cantilevers fractured after a small amount of plastic flow; the fracture toughness of the δ-hydride was found to be 3.3 ± 0.4 MPam1/2 and SEM examination showed transgranular cleavage on the fracture surfaces. Cantilevers notched at the Zr-hydride interface developed interfacial voids during loading, at loads considerably lower than that which initiate brittle fracture of hydrides.

  7. Numerical simulation and performance test of metal hydride hydrogen storage system

    Directory of Open Access Journals (Sweden)

    Tzu-Hsiang Yen, Bin-Hao Chen, Bao-Dong Chen

    2011-05-01

    Full Text Available Metal hydride reactors are widely used in many industrial applications, such as hydrogen storage, thermal compression, heat pump, etc. According to the research requirement of metal hydride hydrogen storage, the thermal analyses have been implemented in the paper. The metal hydride reaction beds are considered as coupled cylindrical tube modules which combine the chemical absorption and desorption in metal hydride. The model is then used metal hydride LaNi5 as an example to predict the performance of metal hydride hydrogen storage devices, such as the position of hydration front and the thermal flux. Under the different boundary condition the characteristics of heat transfer and mass transfer in metal hydride have influence on the hydrogen absorption and desorption. The researches revealed that the scroll design can improve the temperature distribution in the reactor and the porous tube for directing hydrogen can increase the penetration depth of hydride reaction to decrease the hydrogen absorption time.

  8. Sodium-based hydrides for thermal energy applications

    Science.gov (United States)

    Sheppard, D. A.; Humphries, T. D.; Buckley, C. E.

    2016-04-01

    Concentrating solar-thermal power (CSP) with thermal energy storage (TES) represents an attractive alternative to conventional fossil fuels for base-load power generation. Sodium alanate (NaAlH4) is a well-known sodium-based complex metal hydride but, more recently, high-temperature sodium-based complex metal hydrides have been considered for TES. This review considers the current state of the art for NaH, NaMgH3- x F x , Na-based transition metal hydrides, NaBH4 and Na3AlH6 for TES and heat pumping applications. These metal hydrides have a number of advantages over other classes of heat storage materials such as high thermal energy storage capacity, low volume, relatively low cost and a wide range of operating temperatures (100 °C to more than 650 °C). Potential safety issues associated with the use of high-temperature sodium-based hydrides are also addressed.

  9. Hydrothermal synthesis of cerium titanate nanorods and its application in visible light photocatalysis

    International Nuclear Information System (INIS)

    Highlights: • Cerium titanate nanorods have been synthesized by a simple hydrothermal process. • The size of the cerium titanate nanorods can be controlled by growth conditions. • Cerium titanate nanorods exhibit good photocatalytic activities for methyl blue. - Abstract: Cerium titanate nanorods have been prepared via a hydrothermal process using sodium dodecyl sulfate (SDS) as the surfactant. The cerium titanate nanorods have been analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), and ultraviolet–visible (UV–vis) diffuse reflectance spectrum. XRD shows that the nanorods are composed of CeTi21O38 phase. Electron microscopy observations indicate that the nanorods have good single crystalline nature. The diameter and length of the nanorods are about 50–200 nm and 1–2 μm, respectively. Cerium titanate nanorods have a band gap of 2.65 eV. The photocatalytic activities of the nanorods have been investigated by degrading methylene blue (MB) under visible light irradiation. MB solution with the concentration of 10 mg L−1 can be degraded totally with the irradiation time increasing to 240 min. Cerium titanate nanorods exhibit great potential in photocatalytic degradation of MB under visible light irradiation

  10. An environmentally compliant cerium-based conversion coating for aluminum protection

    Science.gov (United States)

    Lin, Xuan

    Chromate conversion coatings have been extensively used in the aircraft industry for the corrosion protection of aluminum alloys. Unfortunately, hexavalent chromium, which is a primary component in the chromating process, is a confirmed carcinogen. Because of rising remediation and disposal costs caused by increasingly strict regulations, the replacement of the traditional chromate conversion process is becoming a top priority in the metal finishing industry. This research focused on the electrodeposition of cerium-based coatings on 7075-T6 aluminum alloy in an electrolyte containing a cerium salt, an oxidizing agent and an organic solvent. The cerium-rich deposits were characterized by phase composition, oxidation state, coating thickness, surface morphology, deposition mechanism and polarization behavior. Chemical and electrochemical tests were utilized to compare the corrosion resistance between cerium-based coatings and chromate conversion coatings. To characterize and simulate the deposition process, a variety of approaches were utilized to study the oxidation states of cerium in various soluble and precipitated forms as a function of hydrogen peroxide and electrolyte pH. The pH ranges where the oxidation and reduction reactions dominate were determined. Further studies were performed to optimize the corrosion performance of cerium-based coatings and to understand the effects of electrolyte constituents and deposition parameters. The optimum levels for these variables were identified. A patent disclosure on the cerium-based coating process was made to the University of Missouri-Rolla and has now been officially filed with the U.S. Patent Office.

  11. X-ray absorption study of cerium in the passive film on aluminum

    International Nuclear Information System (INIS)

    The corrosion-resistance of aluminum-based alloys and metal-matrix composites can be increased by treatment with cerium compounds. Immersion in a 1000 ppm solution of Ce Cl3 for periods of several days has been shown to increase the pitting potential and reduce the corrosion rate. Such treatment is being considered as an alternative to the use of chromate conversion coatings. The protective action of cerium is considered to be due to the formation of a film containing cerium oxide/hydroxide with cerium in the oxidation states 3 and 4. This occurs by precipitation of cerium compounds onto cathodic sites due to the increase of pH associated with oxygen reduction. Cerium compounds are considerably less soluble than aluminum compounds at high pH. It is proposed that the cerium oxide/hydroxide creates a barrier to the reduction of oxygen stifling cathodic reaction with a corresponding reduction in corrosion rate and open circuit potential. Glancing angle x-ray techniques are well-suited to studying the composition and structure of surface layers on materials. X-rays incident at very small angles (of the order of milliradians) below the critical angle do not penetrate beyond the surface layers of the material. With the extremely high brightness beams of x-rays provided by synchrotron sources the authors detect and characterize the chemical state of elements present in low concentrations in the surface of materials

  12. The solubility of cerium in La2Ti2O7 by DFT + U calculations

    International Nuclear Information System (INIS)

    To investigate the solubility of cerium in La2Ti2O7, the density functional theory plus Hubbard U correction (DFT + U) approach is employed. The geometrical structure, solution energy and electronic structure of La2−yCeyTi2O7 (0 ≤ y ≤ 2) have been analyzed. The results reveal that the La2Ti2O7–Ce2Ti2O7 solid solution exits over the entire range of cerium content. The calculated increase in the O48f positional parameter, x, with increasing cerium content, may indicate the increased radiation resistance. The results of the density of states distribution and the Bader charge for each ion in La2Ti2O7–Ce2Ti2O7 solid solution suggest that cerium exhibits a reduced charge state in the solid solution. - Highlights: • La2Ti2O7–Ce2Ti2O7 solid solution exits over the entire range of cerium content from 0 to 2. • Cerium incorporation in La2Ti2O7 may lead to increased radiation resistance of La2−yCeyTi2O7 (0 ≤ y ≤ 2) . • Cerium in the solid solution of La2−yCeyTi2O7 (0 ≤ y ≤ 2) exhibits a reduced charge state

  13. Novel in situ coordinated cerium salt/acrylonitrile-butadiene rubber composite

    International Nuclear Information System (INIS)

    A novel rubber composite of acrylonitrile-butadiene rubber (NBR) filled with cerium salt particles was vulcanized via in situ coordination for the first time. The resulting materials exhibit good mechanical properties. Curing characteristics analysis, differential scanning calorimetry, X-ray photoelectron spectroscopy, tensile testing, and an equilibrium swelling method were used for the characterization of the composite. The results in this paper indicate that the composite is a kind of elastomer based on the in situ coordination crosslinking interactions between the nitrile groups (–CN) of NBR and cerium ions. The mechanical properties of vulcanized cerium salt/ NBR rubber are altered when changing the sorts of cerium salt. Moreover, these materials show good irradiation resistance because of the introduction of the cerium salt. -- Highlights: ► Cerium salts were firstly used to vulcanize the acrylonitrile-butadiene rubber. ► Cerium salts act as not only crosslink agents but also reinforcing fillers in the matrix. ► These materials show good irradiation resistance and mechanical properties at same time.

  14. Characterization of microstructure and catalytic of cerium oxide obtained by colloidal solution

    International Nuclear Information System (INIS)

    This study investigated to obtain particles of cerium oxide, for use as catalysts for the combustion of methane using the technique of through polymeric colloidal solution. Obtaining the colloidal system is based on hydrolysis of salts such as cerium acetylacetonate, cerium nitrate in the presence of additives such as polyvinylbutyral (PVB), polyvinylpyrrolidone (PVP) and polyvinyl acetate (PVA), at concentrations of 5, 10 and 15% in aqueous or alcoholic medium. These solutions containing ions of interest were subjected to a heat treatment at 650° C for 30 minutes, with heating rate of 2 ° C/ min. After heat treatment, the fibers were characterized according to their morphology, surface area, crystallinity, weight loss and catalytic activity. Samples obtained from cerium acetylacetonate were more reactive than the cerium nitrate to the combustion of methane, as showed greater conversions and higher temperatures reached during the process, which is of utmost importance since the combustion catalytic methane is used for generating thermal energy. After the reaction with methane, the samples underwent significant change in surface area, probably due to the intensity of combustion reactions of the nitrate and the generation of heat involved in this reaction, which gave rise to coarse particles. During the combustion process using the obtained from particles of cerium acetylacetonate, there was the release of large quantities of nitrogen compared to the results of assays with the particles obtained with cerium nitrate. (author)

  15. Mesoscopic structure of cerium waste loaded hydrated cement by SANS

    International Nuclear Information System (INIS)

    Cementation is one of the most commonly used methods for conditioning radioactive wastes. It provides a cost-effective solution for encapsulation of low and intermediate level radioactive wastes into suitable solid form for long term safety storage. Cerium is used for decontamination of alpha contaminated metallic waste and after this decontamination process, secondary wastes with corrosion products are created, which must be managed properly and cemented for near surface disposal. In the present work, modification of mesoscopic structure in hydrated cement due to addition of simulated cerium waste at different concentrations has been investigated by small-angle neutron scattering (SANS). Structural modifications, in mesoscopic length scale, have been observed. The scattering profiles for three kinds of cement blocks (virgin, 10 g/l and 20 g/l of corrosion product (C.P.) with 4 mm thickness) are shown. Data have been analyzed in the light of polydisperse spherical particles model assuming a log-normal distribution. Widely separated bimodal particle size distributions best represent the present data. Further, it has been observed that the scattering profile obeys power-law (Q-n) behaviour in two domains of Q, which reflects the self-similar/self-affined morphology of the inhomogeneities. Estimated parameters from SANS data are tabulated. A comparison is shown mentioning the value of scattering radius of gyration, exponent values (η) and average particle size for each kind of hydrated cement sample. (author)

  16. Cerium fluoride nanoparticles protect cells against oxidative stress

    Energy Technology Data Exchange (ETDEWEB)

    Shcherbakov, Alexander B.; Zholobak, Nadezhda M. [Zabolotny Institute of Microbiology and Virology, National Academy of Sciences of Ukraine, Kyiv D0368 (Ukraine); Baranchikov, Alexander E. [Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences, Moscow 119991 (Russian Federation); Ryabova, Anastasia V. [Prokhorov General Physics Institute of the Russian Academy of Sciences, Moscow 119991 (Russian Federation); National Research Nuclear University MEPhI (Moscow Engineering Physics Institute), Moscow 115409 (Russian Federation); Ivanov, Vladimir K., E-mail: van@igic.ras.ru [Kurnakov Institute of General and Inorganic Chemistry of the Russian Academy of Sciences, Moscow 119991 (Russian Federation); National Research Tomsk State University, Tomsk 634050 (Russian Federation)

    2015-05-01

    A novel facile method of non-doped and fluorescent terbium-doped cerium fluoride stable aqueous sols synthesis is proposed. Intense green luminescence of CeF{sub 3}:Tb nanoparticles can be used to visualize these nanoparticles' accumulation in cells using confocal laser scanning microscopy. Cerium fluoride nanoparticles are shown for the first time to protect both organic molecules and living cells from the oxidative action of hydrogen peroxide. Both non-doped and terbium-doped CeF{sub 3} nanoparticles are shown to provide noteworthy protection to cells against the vesicular stomatitis virus. - Highlights: • Facile method of CeF{sub 3} and CeF{sub 3}:Tb stable aqueous sols synthesis is proposed. • Naked CeF{sub 3} nanoparticles are shown to be non-toxic and to protect cells from the action of H{sub 2}O{sub 2}. • CeF{sub 3} and CeF{sub 3}:Tb nanoparticles are shown to protect living cells against the vesicular stomatitis virus.

  17. Sorption removal of arsenic by cerium-exchanged zeolite P

    International Nuclear Information System (INIS)

    Modification of zeolite P was performed by exchanged of its sodium with cerium(III). The resulting cerium-exchanged zeolite P, (CeZP) did not change in its crystallinity compared to original zeolite. The CeZP was subsequently used to sorb As(V) from aqueous solution. Maximum sorption of As(V) by CeZP occurred at pH range 3-10. In addition, the sorption capacity increased with increasing initial As(V) concentrations. The sorption follows Langmuir model with maximum sorption capacity of 8.72 mg g-1 at 25 deg. C and increased to 23.42 mg g-1 at 90 deg. C, indicating an endothermic process. The arsenic sorption by CeZP was not affected by the present of nitrate, chloride, sulphate, carbonate and bromide but was reduced significantly in the presence of phosphate. This study shows that the as prepared CeZP was found effective for the removal of arsenic from wastewater sample of wood treatment industry

  18. New sunscreen materials based on amorphous cerium and titanium phosphate

    International Nuclear Information System (INIS)

    Cerium-titanium pyrophosphates Ce1-xTi xP2O7 (with x = 0, 0.50, and 1.0), which are novel phosphate materials developed as UV-shielding agents for use in cosmetics, were characterized by X-ray diffraction, X-ray fluorescent analysis, UV-vis reflectance, and Raman spectroscopy. Since the optical reflectance shifted to lower wavelengths by the crystallization of the phosphates and the stabilization of the amorphous state of the cerium-titanium pyrophosphates was carried out by doping niobium (Nb). Raman spectroscopic study of the phosphate showed that P-O-P bending and stretching modes decreased with the loading of Nb, accompanying with the formation of Nb-O stretching mode. Therefore, the increase in the amount of the non-bridging oxygen in the amorphous phosphate should be the reason for the inhibition of the crystallization. This stabilization is a significant improvement, which enables to apply these amorphous phosphates not only to cosmetics and paints, but also plastics and films

  19. Altering properties of cerium oxide thin films by Rh doping

    International Nuclear Information System (INIS)

    Highlights: • Thin films of ceria doped by rhodium deposited by RF magnetron sputtering. • Concentration of rhodium has great impact on properties of Rh–CeOx thin films. • Intensive oxygen migration in films with low concentration of rhodium. • Oxygen migration suppressed in films with high amount of Rh dopants. - Abstract: Ceria containing highly dispersed ions of rhodium is a promising material for catalytic applications. The Rh–CeOx thin films with different concentrations of rhodium were deposited by RF magnetron sputtering and were studied by soft and hard X-ray photoelectron spectroscopies, Temperature programmed reaction and X-ray powder diffraction techniques. The sputtered films consist of rhodium–cerium mixed oxide where cerium exhibits a mixed valency of Ce4+ and Ce3+ and rhodium occurs in two oxidation states, Rh3+ and Rhn+. We show that the concentration of rhodium has a great influence on the chemical composition, structure and reducibility of the Rh–CeOx thin films. The films with low concentrations of rhodium are polycrystalline, while the films with higher amount of Rh dopants are amorphous. The morphology of the films strongly influences the mobility of oxygen in the material. Therefore, varying the concentration of rhodium in Rh–CeOx thin films leads to preparing materials with different properties

  20. Cerium compounds in the fashion of the light actinides

    International Nuclear Information System (INIS)

    Researchers familiar with the light actinides easily recognize in cerium compounds a microcosm of the rich variety of properties seen in the light actinides. The parallelism seen between comparable cerium and actinide compounds strongly suggests that the same physical models are applicable. The most significant is the relative size of the f-orbital. Localization is generally tighter in Ce compounds than uranium compounds, making Ce roughly analogous to Np through Am. A way to see the actinide parallelism is to compare Hill plots. Compounds in the different regions of the plots (representing different physics) are isostructural compounds with the same companion (B) elements. The most common materials exhibiting a direct f-f interaction are the cubic Laves compounds. Accordingly, we have determined the band structures of CeRu2, CeRh2, CeIr2, CeOs2, and CeNi2. Compounds illustrative of the interaction of f-orbitals with ligand orbitals are the Cu3Au structured materials. Materials calculated in this class are CeRh3, CePd3, and CeSn3 - the materials of much interest as mixed valent. Although the focus is on the Ce compounds, calculations performed on uranium isomorphs are used to highlight the interesting physics

  1. Spectrophotometric determination of Cerium from Monazite Bangka using Tiron reagent

    International Nuclear Information System (INIS)

    To anticipate the analysis of individual rare earth element from monazite processing which have done at PTPBGN division and samples from other division of P2BGN, and to develop the Ce analysis method by spectrophotometric using tiron reagent. The purpose of the experiment is to find out the method and the condition of Ce analysis with high accuracy and applicable. The variable observation were cerium-tiron spectrum, pH, ligand concentration, buffer concentration, linearity, anion influence, limit detection, impurities of elements and complex stability. The complex of cerium-tiron produce the maximum absorption at 497.5 nm and stable until 8 hours. The optimum conditions of this method was : tiron concentration is 0.25 %, pH 8.5 with buffer solution sodium acetate is 0.3 M. Detection limit is 1.00 ppm and area of linearity between 1 - 100 ppm, and PO4, Fe, U and Ti was influence to this method. The content of Ce from 2 samples of monazite Bangka which determine by this method was 18%

  2. Cerium fluoride nanoparticles protect cells against oxidative stress

    International Nuclear Information System (INIS)

    A novel facile method of non-doped and fluorescent terbium-doped cerium fluoride stable aqueous sols synthesis is proposed. Intense green luminescence of CeF3:Tb nanoparticles can be used to visualize these nanoparticles' accumulation in cells using confocal laser scanning microscopy. Cerium fluoride nanoparticles are shown for the first time to protect both organic molecules and living cells from the oxidative action of hydrogen peroxide. Both non-doped and terbium-doped CeF3 nanoparticles are shown to provide noteworthy protection to cells against the vesicular stomatitis virus. - Highlights: • Facile method of CeF3 and CeF3:Tb stable aqueous sols synthesis is proposed. • Naked CeF3 nanoparticles are shown to be non-toxic and to protect cells from the action of H2O2. • CeF3 and CeF3:Tb nanoparticles are shown to protect living cells against the vesicular stomatitis virus

  3. The van Hemmen-Kondo model for disordered cerium systems

    International Nuclear Information System (INIS)

    The interplay between disorder and strong correlations has been observed experimentally in disordered cerium alloys such as Ce(Ni, Cu) or Ce(Pd, Rh). In the case of Ce(Ni, Cu) alloys with a Cu concentration x between 0.6 and 0.3, the first studies have shown a smooth transition with decreasing temperature from a spin glass phase to ferromagnetism; for x smaller than 0.2, a Kondo phase has been observed. The situation is more complicated now due to the recent observation of magnetic clusters. The competition between the Kondo effect, the spin glass (SG) and the ferromagnetic (FE) ordering has been extensively studied theoretically. The Kondo effect is described by the usual mean-field approximation; we have treated the SG behavior successively by the Sherrington-Kirkpatrick model, then by the Mattis model and finally by the van Hemmen model, which takes both a ferromagnetic part and a site-disorder random part for the intersite exchange interaction. We present here the results obtained by the van Hemmen-Kondo model: for a large Kondo exchange JK, a Kondo phase is obtained while, for smaller JK, the succession of an SG phase, a mixed SG-FE one and finally an FE one has been obtained with decreasing temperature. This model improves the theoretical description of disordered Kondo systems by providing a simpler approach for further calculations of magnetic clusters and can, therefore, account for recent experimental data on disordered cerium systems.

  4. New sunscreen materials based on amorphous cerium and titanium phosphate

    Energy Technology Data Exchange (ETDEWEB)

    Masui, Toshiyuki [Department of Applied Chemistry, Faculty of Engineering and Handai Frontier Research Center, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Hirai, Hidekazu [Department of Applied Chemistry, Faculty of Engineering and Handai Frontier Research Center, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan); Imanaka, Nobuhito [Department of Applied Chemistry, Faculty of Engineering and Handai Frontier Research Center, Osaka University, 2-1 Yamadaoka, Suita, Osaka 565-0871 (Japan)]. E-mail: imanaka@chem.eng.osaka-u.ac.jp; Adachi, Gin-ya [Juri Institute for Environmental Science and Chemistry, College of Analytical Chemistry, 2-1-8 Temma, Kita-ku, Osaka 530-0043 (Japan)

    2006-02-09

    Cerium-titanium pyrophosphates Ce{sub 1-x}Ti {sub x}P{sub 2}O{sub 7} (with x = 0, 0.50, and 1.0), which are novel phosphate materials developed as UV-shielding agents for use in cosmetics, were characterized by X-ray diffraction, X-ray fluorescent analysis, UV-vis reflectance, and Raman spectroscopy. Since the optical reflectance shifted to lower wavelengths by the crystallization of the phosphates and the stabilization of the amorphous state of the cerium-titanium pyrophosphates was carried out by doping niobium (Nb). Raman spectroscopic study of the phosphate showed that P-O-P bending and stretching modes decreased with the loading of Nb, accompanying with the formation of Nb-O stretching mode. Therefore, the increase in the amount of the non-bridging oxygen in the amorphous phosphate should be the reason for the inhibition of the crystallization. This stabilization is a significant improvement, which enables to apply these amorphous phosphates not only to cosmetics and paints, but also plastics and films.

  5. Influence of Specific Surface Area of Powder on Hydrogen Desorption Kinetics for Metal Hydrides

    CERN Document Server

    Drozdov, I V

    2014-01-01

    The observable results for desorption kinetics by powder of metal hydride on the example of mangesium hydride are reproduced with the model formulated in terms of specific surface of powder. A volumetric measurement of hydrogen desorption process is evaluated on an example of wet ball milled magnesium hydride, and can be applied generally for any metal hydride. The exact solution of the model reproduces the shape of experimental curves for desorption process providing a satisfying agreement with experimental data.

  6. [Ion chromatography of L-ascorbic acid, sulfite and thiosulfate using their postcolumn reactions with cerium (IV) and fluorescence detection of cerium (III)].

    Science.gov (United States)

    Chen, Q; Hu, K; Miura, Y

    1999-09-01

    An ion chromatographic method was used to separate the species of L-ascorbic acid, sulfite and thiosulfate in their mixtures. This method is based on the separation of each anion in their mixtures by using a separation column, and then on the fluorimetric measurement of cerium (III) formed by a postcolumn reaction of cerium (IV) with the species of L-ascorbic acid, sulfite and thiosulfate in the effluent. The optimal conditions for separating and determining the above three species have been established. By using a 3 mmol/L carbonate eluent, the species of L-ascorbic acid, sulfite and thiosulfate could be eluted at the proper retention times of 1.7, 2.6 and 5.0 min, respectively, and these three anions could be separated completely. The effects of the concentrations of cerium (IV) and sulfuric acid in the postcolumn reaction solution on the chromatographic peak-height were tested in order to obtain the optimal peak-height. It was found that the peak-height at first increases rapidly with an increase in the concentration of cerium (IV) and sulfuric acid respectively up to a certain concertation, then increases slowly. These critical concentrations of cerium (IV) and sulfuric acid also depend on the amount of the analyte injected. Meanwhile the baseline signals of the sepectra increase with an increase in the concentration of cerium (IV). Some concentrations above the critical concentration of sulfuric acid could be selected as the optimal concentration of sulfuric acid, but the concentration of cerium (IV) should be optimized by establishing a compromise between the higher peak-height and the lower baseline signal. The detection limit of this method was found to be 1 mumol/L for thiosulfate when an amount of 100 microL analyte was injected. PMID:12552889

  7. A study of advanced magnesium-based hydride and development of a metal hydride thermal battery system

    Science.gov (United States)

    Zhou, Chengshang

    Metal hydrides are a group of important materials known as energy carriers for renewable energy and thermal energy storage. A concept of thermal battery based on advanced metal hydrides is studied for heating and cooling of cabins in electric vehicles. The system utilizes a pair of thermodynamically matched metal hydrides as energy storage media. The hot hydride that is identified and developed is catalyzed MgH2 due to its high energy density and enhanced kinetics. TiV0.62Mn1.5, TiMn2, and LaNi5 alloys are selected as the matching cold hydride. A systematic experimental survey is carried out in this study to compare a wide range of additives including transitions metals, transition metal oxides, hydrides, intermetallic compounds, and carbon materials, with respect to their effects on dehydrogenation properties of MgH2. The results show that additives such as Ti and V-based metals, hydride, and certain intermetallic compounds have strong catalytic effects. Solid solution alloys of magnesium are exploited as a way to destabilize magnesium hydride thermodynamically. Various elements are alloyed with magnesium to form solid solutions, including indium and aluminum. Thermodynamic properties of the reactions between the magnesium solid solution alloys and hydrogen are investigated, showing that all the solid solution alloys that are investigated in this work have higher equilibrium hydrogen pressures than that of pure magnesium. Cyclic stability of catalyzed MgH2 is characterized and analyzed using a PCT Sievert-type apparatus. Three systems, including MgH2-TiH 2, MgH2-TiMn2, and MgH2-VTiCr, are examined. The hydrogenating and dehydrogenating kinetics at 300°C are stable after 100 cycles. However, the low temperature (25°C to 150°C) hydrogenation kinetics suffer a severe degradation during hydrogen cycling. Further experiments confirm that the low temperature kinetic degradation can be mainly related the extended hydrogenation-dehydrogenation reactions. Proof

  8. Structural, topographical and electrical properties of cerium doped strontium barium niobate (Ce:SBN60) ceramics

    Science.gov (United States)

    Raj, S. Gokul; Mathivanan, V.; Kumar, G. Ramesh; Yathavan, S.; Mohan, R.

    2016-05-01

    Tungsten bronze type cerium doped strontium barium niobate (Ce:SBN - Sr0.6B0.4Nb2O6) ceramics were synthesized by solid state process. Cerium was used as dopant to improve its electrical properties. Influence of Ce+ ions on the photoluminescence properties was investigated in detail. The grain size topographical behavior of SBN powders and their associated abnormal grain growth (AGG) were completely analyzed through SEM studies. Finally dielectric, measurement discusses about the broad phase transition observed due to cerium dopant The results were discussed in detail.

  9. Violet/blue emission from epitaxial cerium oxide films on silicon substrates

    International Nuclear Information System (INIS)

    Violet/blue photoluminescence was observed from epitaxial cerium oxide films on silicon substrates. The films were deposited on silicon (111) substrates under ultrahigh vacuum conditions using pulsed laser ablation of a cerium oxide target and treated by rapid thermal annealing in argon. High resolution transmission electron microscopy and x-ray diffraction measurements indicated the formation of a single crystal cerium oxide phase Ce6O11 different from CeO2 in the annealed films. The emission might be due to charge transfer transitions from the 4f band to the valence band of the oxide. copyright 1997 American Institute of Physics

  10. The study on preparation of high dispersion and pure cerium dioxide for producing automotive exhaust catalysts

    International Nuclear Information System (INIS)

    The multi-stage counter-current solvent extraction process using TBP as the solvent has been carried out for purifying cerium and the ammonium carbonate precipitation method has been used to produce the cerium oxide of high dispersion and pure. The flow sheet of extraction system includes 3 extraction stages with O/A = 0.7,2 stripping stages and 4 scrubbing stages with O/A = 5. The condition for ammonium carbonate precipitation, drying and calcination have been investigated and a procedure that seem to be practically suitable to prepare cerium dioxide powder with great specific surface area for producing automotive exhaust catalyst has been proposed. (LMT)

  11. Effect of Cerium on Mechanical Properties and Morphology of ZZn4-1 Alloy

    Institute of Scientific and Technical Information of China (English)

    2000-01-01

    Effect of the addition of cerium in appropriate amount on the mechanical properties and morphology of ZZn4-1 alloy was investigated. In the case of samples collected from metal mould, the results show that the addition of cerium in appropriate amount can increase tensile strength and HB hardness, and can refine the microstructure of ZZn4-1 alloy considerably. In the case of samples collected from pressure die-casting, the addition of cerium in appropriate amount can refine the primary η-phase and the eutectic structure of pressure die-casting and improve mechanical and processing properties of the alloy.

  12. Ion exchange reactions in amorphous and crystalline aluminium silicates from solution of cerium salts

    International Nuclear Information System (INIS)

    Reactions of ion-exchange of Na+ by Ce3+ and NH4+ on the zeolite containing catalyst, amorphous silica alumina and zeolite Y have been studied. The cerium cations are shown to be exchanged by the Na+ cations with more selectivity than the anmonia cations. In the case of the zeolite containing catalyst and amorphous silica alumina the region of the staggered ion-exchange from the mixture of the solutions of cerium and ammonium sulphates was been detected. This is explained by the formation fo cerium complexes with the sulphate ions

  13. A metal hydride-polymer composite for hydrogen storage applications

    International Nuclear Information System (INIS)

    To address the issue of the breakdown into fine powders that occurs in the practical use of metal hydrides, the possibility of using a polymeric material as a matrix that contains the active metal particles was experimentally assessed. A ball milling approach in the tumbling mode was used to develop a metal hydride-polymer composite with a high metal to polymer weight ratio. The alloy powder was blended with the polymer and a coating of the metal particles was obtained. The composite was consolidated by hot pressing and the pellets were characterized in terms of their hydriding-dehydriding properties. The materials did not show significant losses in either loading capacity or kinetic properties. The polymeric matrix resulted as being stable under hydrogen cycling. Further, from SEM observation it was confirmed that the metal powders remained embedded in the polymeric matrix even after a number of cycles and that the overall dimensional integrity was retained.

  14. Theoretical Estimate of Hydride Affinities of Aromatic Carbonyl Compounds

    Institute of Scientific and Technical Information of China (English)

    AI Teng; ZHU Xiao-Qing; CHENG Jin-Pei

    2003-01-01

    @@ Aromatic carbonyl compounds are one type of the most important organic compounds, and the reductions ofthem by hydride agents such as LiAlH4 or NaBH4 are widely used in organic synthesis. The reactivity of carbonyl compounds generally increases in the following order: ketone < aldehyde, and amide < acid < ester < acid halide, which could be related to their hydride affinities (HA). In the previous paper, Robert[1] calculated the absolute HAof a series of small non-aromatic carbonyl compounds. In this paper, we use DFT method at B3LYP/6-311 + + G (2d, 2p)∥B3LYP/6-31 + G* level to estimate hydride affinities of five groups of aromatic carbonyl compounds. The detailed results are listed in Table 1.

  15. Infrared diode laser spectroscopy of lithium hydride

    International Nuclear Information System (INIS)

    The fundamental and hot bands of the vibration--rotation transitions of 6 LiH, 7 LiH, 6 LiD, and 7 LiD were observed by infrared diode laser spectroscopy at Doppler-limited resolution. Lithium hydride molecules were produced by the reaction of the Li vapor with hydrogen at elevated temperatures. Some 40 transitions were observed and, after combined with submillimeter-wave spectra reported by G. M. Plummer et al. [J. Chem. Phys. 81, 4893 (1984)], were analyzed to yield Dunham-type constants with accuracies more than an order of magnitude higher than those published in the literature. It was clearly demonstrated that the Born--Oppenheimer approximation did not hold, and some parameters representing the breakdown were evaluated. The Born--Oppenheimer internuclear distance r/sup BO//sub e/ was derived to be 1.594 914 26 (59) A, where a new value of Planck's constant recommended by CODATA was employed. The relative intensity of absorption lines was measured to determine the ratio of the permanent dipole moment to its first derivative with respect to the internuclear distance: μ/sub e/ [(partialμpartialr)/sub e/ r/sub e/ ] = 1.743(86). The pressure broadening parameter Δν/sub p/ P was determined to be 6.40 (22) MHzTorr by measuring the linewidth dependence on the pressure of hydrogen, which was about four times larger than the value for the dipole--quadrupole interaction estimated by Kiefer and Bushkovitch's theory

  16. High-Spin Cobalt Hydrides for Catalysis

    Energy Technology Data Exchange (ETDEWEB)

    Holland, Patrick L. [Yale University

    2013-08-29

    Organometallic chemists have traditionally used catalysts with strong-field ligands that give low-spin complexes. However, complexes with a weak ligand field have weaker bonds and lower barriers to geometric changes, suggesting that they may lead to more rapid catalytic reactions. Developing our understanding of high-spin complexes requires the use of a broader range of spectroscopic techniques, but has the promise of changing the mechanism and/or selectivity of known catalytic reactions. These changes may enable the more efficient utilization of chemical resources. A special advantage of cobalt and iron catalysts is that the metals are more abundant and cheaper than those currently used for major industrial processes that convert unsaturated organic molecules and biofeedstocks into useful chemicals. This project specifically evaluated the potential of high-spin cobalt complexes for small-molecule reactions for bond rearrangement and cleavage reactions relevant to hydrocarbon transformations. We have learned that many of these reactions proceed through crossing to different spin states: for example, high-spin complexes can flip one electron spin to access a lower-energy reaction pathway for beta-hydride elimination. This reaction enables new, selective olefin isomerization catalysis. The high-spin cobalt complexes also cleave the C-O bond of CO2 and the C-F bonds of fluoroarenes. In each case, the detailed mechanism of the reaction has been determined. Importantly, we have discovered that the cobalt catalysts described here give distinctive selectivities that are better than known catalysts. These selectivities come from a synergy between supporting ligand design and electronic control of the spin-state crossing in the reactions.

  17. Dissolution and Precipitation Temperatures of δ Hydrides in Zirconium

    International Nuclear Information System (INIS)

    Anelastic effects due to the formation and dissolution of hydrides on crystal bar Zirconium (O-6 and 2x10-5 , in a gaseous atmosphere (He) to allow a better thermal conductivity inside the pendulum.Hydriding was achieved inside the pendulum by the inlet of hydrogen gas.The final hydrogen contents was determined by fusion analysis and resulted in 36 ppm.The first ''in situ'' hydriding is obtained by introducing an hydrogen pressure of 60kPa in the pendulum during 1h at 295K. Then, the hydrogen atmosphere is extracted by mechanical vacuum and an helium atmosphere is reinserted.The IF and G measurements are made in this condition. During the first heating an anomaly at 430K and a little step in the modulus G are obtained, indicating a d dissolution temperature TSSD of 430K for 8.6 wt ppm of H.After a solubilization of 10min at 495K, there are simultaneous effects: a step in G and an IF peak which is not enough developed on its right side.They presume a d precipitation temperature TSSP of 485K for 20 wt ppm of H. After a 1h at 490K, the peaks are again obtained with slight changes.The second ''in situ'' hydration during 8h at 173K, give rise to several peaks and modulus variations in the temperature range (300-400)K which are assessed to be due to transitions occurring to metastable γ and ε hydrides formed upon hydriding at low temperature, and to the δ hydride

  18. Photoelectron spectroscopy of boron aluminum hydride cluster anions

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Haopeng; Zhang, Xinxing; Ko, Yeon Jae; Gantefoer, Gerd; Bowen, Kit H., E-mail: kbowen@jhu.edu, E-mail: kiran@mcneese.edu [Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218 (United States); Li, Xiang [Center for Space Science and Technology, University of Maryland–Baltimore County, Baltimore, Maryland 21250 (United States); Kiran, Boggavarapu, E-mail: kbowen@jhu.edu, E-mail: kiran@mcneese.edu [Department of Chemistry and Physics, McNeese State University, Lake Charles, Louisiana 70609 (United States); Kandalam, Anil K. [Department of Physics, West Chester University, West Chester, Pennsylvania 19383 (United States)

    2014-04-28

    Boron aluminum hydride clusters are studied through a synergetic combination of anion photoelectron spectroscopy and density functional theory based calculations. Boron aluminum hydride cluster anions, B{sub x}Al{sub y}H{sub z}{sup −}, were generated in a pulsed arc cluster ionization source and identified by time-of-flight mass spectrometry. After mass selection, their photoelectron spectra were measured by a magnetic bottle-type electron energy analyzer. The resultant photoelectron spectra as well as calculations on a selected series of stoichiometries reveal significant geometrical changes upon substitution of aluminum atoms by boron atoms.

  19. Energy management of fuel cell electric vehicle with hydrid tanks

    OpenAIRE

    Ravey, Alexandre; FAIVRE, Sébastien; HIGEL, Charles; HAREL, Fabien; Djerdir, Abdesslem

    2014-01-01

    This paper proposes a novel control strategy for fuel cell electric vehicle including hydrid tanks using fuzzy logic controller. The aim of the study is to manage both thermal and electric energy with the same controller in order to use the fuel cell system as a range extender by preventing the batteries state of charge to drop too quickly. The presented controller use both batteries state of charge and thermal status of hydrid tank to control the fuel cell power. This work is a part of the M...

  20. Hydriding and dehydriding properties of CaSi

    International Nuclear Information System (INIS)

    The hydriding and dehydriding properties of CaSi were investigated both theoretically and experimentally. First-principles calculations suggested that CaSiH n is thermodynamically stable. Experimentally, the p -c isotherms clearly demonstrated plateau pressures in a temperature range of 473-573 K and the maximum hydrogen content was 1.9 weight % (wt.%) under a hydrogen pressure of 9 MPa at 473 K. The structure of CaSiH n is different from those of ZrNi hydrides, although CaSi has the CrB-type structure as well as ZrNi

  1. Studies of solution deposited cerium oxide thin films on textured Ni-alloy substrates for YBCO superconductor

    International Nuclear Information System (INIS)

    Cerium oxide (CeO2) buffer layers play an important role for the development of YBa2Cu3O7-x (YBCO) based superconducting tapes using the rolling assisted biaxially textured substrates (RABiTS) approach. The chemical solution deposition (CSD) approach has been used to grow epitaxial CeO2 films on textured Ni-3 at.% W alloy substrates with various starting precursors of ceria. Precursors such as cerium acetate, cerium acetylacetonate, cerium 2-ethylhexanoate, cerium nitrate, and cerium trifluoroacetate were prepared in suitable solvents. The optimum growth conditions for these cerium precursors were Ar-4% H2 gas processing atmosphere, solution concentration levels of 0.2-0.5 M, a dwell time of 15 min, and a process temperature range of 1050-1150 deg. C. X-ray diffraction, AFM, SEM, and optical microscopy were used to characterize the CeO2 films. Highly textured CeO2 layers were obtained on Ni-W substrates with both cerium acetate and cerium acetylacetonate as starting precursors. YBCO films with a J c of 1.5 MA/cm2 were obtained on cerium acetylacetonate-based CeO2 films with sputtered YSZ and CeO2 cap layers

  2. Exploring "aerogen-hydride" interactions between ZOF2 (Z = Kr, Xe) and metal hydrides: An ab initio study

    Science.gov (United States)

    Esrafili, Mehdi D.; Mohammadian-Sabet, Fariba

    2016-06-01

    In this work, a new σ-hole interaction formed between ZOF2 (Z = Kr and Xe) as the Lewis acid and a series of metal-hydrides HMX (M = Be, Mg, Zn and X = H, F, CN, CH3) is reported. The nature of this interaction, called "aerogen-hydride" interaction, is unveiled by molecular electrostatic potential, non-covalent interaction, quantum theory of atoms in molecules and natural bond orbital analyses. Our results indicate that the aerogen-hydride interactions are quite strong and can be comparable in strength to other σ-hole bonds. An important charge-transfer interaction is also associated with the formation of OF2Z⋯HMX complexes.

  3. Observations on Hydride Structures at the Tip of Arrested Cracks Grown under Conditions of Delayed Hydride Cracking

    International Nuclear Information System (INIS)

    One sample of Zr2.5%Nb and one sample of cold worked and stress relieved Zircaloy-4 which have been tested for hydrogen induced crack growth have been examined in the crack tip region with the aim of determining the mechanism behind the growth of cracks. The proposed mechanisms are brittle failure of a crack tip hydride and hydrogen enhanced localized shear. The examinations were done by TEM and SEM. However attempts to produce a TEM specimen with a thinned region at the tip of the crack were unsuccessful in both samples. One feature observed in the Zr2.5%Nb material may however be an indication of intense shear deformation at the tip of the crack. On the other hand all observations on the Zircaloy-4 sample indicate precipitation of hydrides ahead of the crack tip and the presence of hydrides on the crack flanks

  4. Chemical Hydride Slurry for Hydrogen Production and Storage

    Energy Technology Data Exchange (ETDEWEB)

    McClaine, Andrew W

    2008-09-30

    The purpose of this project was to investigate and evaluate the attractiveness of using a magnesium chemical hydride slurry as a hydrogen storage, delivery, and production medium for automobiles. To fully evaluate the potential for magnesium hydride slurry to act as a carrier of hydrogen, potential slurry compositions, potential hydrogen release techniques, and the processes (and their costs) that will be used to recycle the byproducts back to a high hydrogen content slurry were evaluated. A 75% MgH2 slurry was demonstrated, which was just short of the 76% goal. This slurry is pumpable and storable for months at a time at room temperature and pressure conditions and it has the consistency of paint. Two techniques were demonstrated for reacting the slurry with water to release hydrogen. The first technique was a continuous mixing process that was tested for several hours at a time and demonstrated operation without external heat addition. Further work will be required to reduce this design to a reliable, robust system. The second technique was a semi-continuous process. It was demonstrated on a 2 kWh scale. This system operated continuously and reliably for hours at a time, including starts and stops. This process could be readily reduced to practice for commercial applications. The processes and costs associated with recycling the byproducts of the water/slurry reaction were also evaluated. This included recovering and recycling the oils of the slurry, reforming the magnesium hydroxide and magnesium oxide byproduct to magnesium metal, hydriding the magnesium metal with hydrogen to form magnesium hydride, and preparing the slurry. We found that the SOM process, under development by Boston University, offers the lowest cost alternative for producing and recycling the slurry. Using the H2A framework, a total cost of production, delivery, and distribution of $4.50/kg of hydrogen delivered or $4.50/gge was determined. Experiments performed at Boston

  5. Coulometric microdetermination of organic compounds with manganese(III) and cerium(IV)

    International Nuclear Information System (INIS)

    The oxidation of compounds such as hydroquinon, p-aminophenol, paracetamol and phenacetin was performed using cerium(IV) and manganese(III) coulometrically electrogenerated. Quantitative results obtained are excellent even at the microscale level. (author)

  6. Immobilization of simulated radioactive soil waste containing cerium by self-propagating high-temperature synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Mao, Xianhe, E-mail: maoxianhe@hotmail.com; Qin, Zhigui; Yuan, Xiaoning; Wang, Chunming; Cai, Xinan; Zhao, Weixia; Zhao, Kang; Yang, Ping; Fan, Xiaoling

    2013-11-15

    A simulated radioactive soil waste containing cerium as an imitator element has been immobilized by a thermite self-propagating high-temperature synthesis (SHS) process. The compositions, structures, and element leaching rates of products with different cerium contents have been characterized. To investigate the influence of iron on the chemical stability of the immobilized products, leaching tests of samples with different iron contents with different leaching solutions were carried out. The results showed that the imitator element cerium mainly forms the crystalline phases CeAl{sub 11}O{sub 18} and Ce{sub 2}SiO{sub 5}. The leaching rate of cerium over a period of 28 days was 10{sup −5}–10{sup −6} g/(m{sup 2} day). Iron in the reactants, the reaction products, and the environment has no significant effect on the chemical stability of the immobilized SHS products.

  7. Immobilization of simulated radioactive soil waste containing cerium by self-propagating high-temperature synthesis

    Science.gov (United States)

    Mao, Xianhe; Qin, Zhigui; Yuan, Xiaoning; Wang, Chunming; Cai, Xinan; Zhao, Weixia; Zhao, Kang; Yang, Ping; Fan, Xiaoling

    2013-11-01

    A simulated radioactive soil waste containing cerium as an imitator element has been immobilized by a thermite self-propagating high-temperature synthesis (SHS) process. The compositions, structures, and element leaching rates of products with different cerium contents have been characterized. To investigate the influence of iron on the chemical stability of the immobilized products, leaching tests of samples with different iron contents with different leaching solutions were carried out. The results showed that the imitator element cerium mainly forms the crystalline phases CeAl11O18 and Ce2SiO5. The leaching rate of cerium over a period of 28 days was 10-5-10-6 g/(m2 day). Iron in the reactants, the reaction products, and the environment has no significant effect on the chemical stability of the immobilized SHS products.

  8. Electroreduction of cerium ions on silver electrode in halide melts at 973 K

    International Nuclear Information System (INIS)

    The mechanism of electroreduction of cerium ions in equimolar KCl-NaCl melt is explored at 973 K. The effect of the anionic composition of the melt on the electroreduction of cerium ions is studied. It is shown that the electrodeposition of cerium metal from halide melts on a silver electrode is the primary electrochemical process that occurs at potentials more positive than those corresponding to the supporting-electrolyte decomposition. The electroreduction of chloride complexes of cerium on a silver electrode in the melt in both steady- and non-steady-state polarization modes at rates below V≤0.5 V/s is controlled by the diffusion delivery; at higher polarization rates, the charge-transfer stage predominates

  9. Electrochemical separation of uranium and cerium in molten LiCl-KCl

    International Nuclear Information System (INIS)

    The electrochemical separation of uranium from cerium in LiCl–KCl eutectic and the electrochemical behavior of Ce(III) were studied. According to the cyclic voltammogram of Ce(III) and the former result of U(III), electrodeposition potential was determined at -1.65 V (vs Ag/AgCl). The uranium metal was successfully deposited and separated from cerium. The morphology of deposit and cross section of electrode were investigated by SEM, firstly uranium deposit alloys with stainless steel and forms a thin transition layer, and secondly the uranium metal layer grows from the transition layer. The separation factors of uranium/cerium on different recovery ratios were determined through a series of steps. It was found that the content of cerium in the deposit and separation factors declined with increasing the initial concentration of U3+ in molten salts; the separation factors remained stable at around 20 in different uranium recovery ratios. (author)

  10. Synergistic extraction of uranium (VI), thorium (IV) and cerium (III) by thenoyltri-fluoroacetone and phenanthroline

    International Nuclear Information System (INIS)

    The synergistic extraction of uranium(VI), thorium(IV) and cerium(III) with thenoyltrifluoroacetone (HTTA) and phenanthroline (phen) is studied. The extraction equilibrium constants are calculated and the mechanism of the synergistic extraction has been discussed

  11. The low gas flow rate foam separation of cerium(III) from dilute aqueous solutions

    International Nuclear Information System (INIS)

    Two low gas flow rate foam separation techniques, ion and precipitate flotation, have been investigated for the separation of trivalent cerium from solutions with initial cerium concentrations ranging from 1 x 10-8 to 1 x 10-4M in the pH range of 1.8 to 12 using the anionic collector sodium lauryl sulphate and the cationic surfactant cetyl trymethyl ammonium bromide. In addition to the type of collector, the pH and the cerium ion concentration, and other factors which can affect flotation results, viz. the time period of bubbling, the rate of gas flow, the ageing of both the cerium and the collector ions, the ionic strength, and the concentration of the collector ions have been investigated and optimum conditions have been established. Under optimum conditions removals as high a 98.5% can be achieved. (author)

  12. Cerium-based conversion coatings to improve the corrosion resistance of aluminium alloy 6061-T6

    International Nuclear Information System (INIS)

    Highlights: • Cerium-based conversion coatings. • Cerium salt sources assisted with hydrogen peroxide. • Protective properties of the conversion coating. - Abstract: Cerium-based conversion coatings were deposited on aluminium alloy 6061-T6 by immersion in two cerium salt sources (chloride- and nitrate-based) assisted with hydrogen peroxide (H2O2). The morphology and composition of the coatings were analysed using scanning electron microscopy and energy dispersive X-ray spectroscopy. Electrochemical measurements to assess corrosion behaviour were performed using free corrosion potential, polarisation and electrochemical impedance spectroscopy with a 3% NaCl solution. The influence of H2O2 on the generation of the coating was studied by cyclic voltammetry tests. The protective properties of the coating generated are heavily dependent upon the chelating effect, chaotropic anion, the pH and H2O2 content

  13. Synergistic inhibition of carbon steel corrosion in seawater by cerium chloride and sodium gluconate

    International Nuclear Information System (INIS)

    Highlights: • Significant synergistic effect was determined for cerium and gluconate. • The mixture showed significant corrosion inhibition of carbon steel in seawater. • Predominant anodic inhibition mechanism was observed. • The presence of cerium ions incorporated in the protective layer was confirmed. - Abstract: In this research the effect of cerium (III) chloride heptahydrate (CC) and sodium gluconate (SG) on the corrosion inhibition of carbon steel C45 (1531) in natural seawater has been evaluated using electrochemical methods and scanning electron microscopy (SEM). The results show that substantial corrosion inhibition (94.98%) using CC and SG can be obtained in synergistic manner. Surface analysis confirmed the presence of cerium ions incorporated in the protective layer of carbon steel specimen. SG acts predominantly as anodic inhibitor whereas CC acts as a mixed type inhibitor. Using both inhibitors predominant mechanism of anodic inhibition is observed

  14. Cerium oxide for the destruction of chemical warfare agents: A comparison of synthetic routes

    Czech Academy of Sciences Publication Activity Database

    Janos, P.; Henych, Jiří; Pelant, O.; Pilařová, V.; Vrtoch, L.; Kormunda, M.; Mazanec, K.; Štengl, Václav

    2016-01-01

    Roč. 304, MAR (2016), s. 259-268. ISSN 0304-3894 Institutional support: RVO:61388980 Keywords : Cerium oxide * Chemical warfare agents * Organophosphate compounds * Decontamination Subject RIV: CA - Inorganic Chemistry Impact factor: 4.529, year: 2014

  15. Direct growth of cerium oxide nanorods on diverse substrates for superhydrophobicity and corrosion resistance

    Science.gov (United States)

    Cho, Young Jun; Jang, Hanmin; Lee, Kwan-Soo; Kim, Dong Rip

    2015-06-01

    Superhydrophobic surfaces with anti-corrosion properties have attracted great interest in many industrial fields, particularly to enhance the thermal performance of offshore applications such as heat exchangers, pipelines, power plants, and platform structures. Nanostructures with hydrophobic materials have been widely utilized to realize superhydrophobicity of surfaces, and cerium oxide has been highlighted due to its good corrosion resistive and intrinsically hydrophobic properties. However, few studies of direct growth of cerium oxide nanostructures on diverse substrates have been reported. Herein we report a facile hydrothermal method to directly grow cerium oxide nanorods on diverse substrates, such as aluminum alloy, stainless steel, titanium, and silicon. Diverse substrates with cerium oxide nanorods exhibited superhydrophobicity with no hydrophobic modifiers on their surfaces, and showed good corrosion resistive properties in corrosive medium. We believe our method could pave the way for realization of scalable and sustainable corrosion resistive superhydrophobic surfaces in many industrial fields.

  16. Studies of boron hydrides: new heteroboranes

    International Nuclear Information System (INIS)

    I. The chemistry of the bipentaborane 2,2'-(B5H8)2 is investigated to some extent. Pyrolysis of 2,2'-(B5H8)2 resulted in the formation of non-volatile solid boron hydrides and hydrogen. Treatment of 2,2'-(B5H8)2 with bromine in the presence of AlBr3 resulted in the isolation of 1,1'Br2-2,2'-(B5H7)2. Reaction of 2,2'-(B5H8)2 with deprotonating agents resulted in the formation of the corresponding anions. Reaction of 2,2'-(B5H8)2 with diborane followed by acidification afforded n-B9H15 and B10H14 in moderate yield. II. Reaction of K+B9H12S- with potassium polyselenide resulted in the isolation of stable white crystals of B9H9SSe. Treatment of B9H9SSe with one equivalent of base in methanol gave the unstable heteroborane B8H9(OCH3)SSE and treatment with two equivalents of base afforded yellow crystals of B7H9SSe. Reaction of K+B9H12S- with arsenic trioxide in aqueous basic solution gave the electron-rich heteroborane, B8H8As2S in moderate yield. This resulted in the isolation and identification of Et3N.BH3 and the new metalloborane B7H7As2SCo(C5H5). Treatment of B10H11Se- with As2O3 resulted in the isolation of the stable nido-heteroborane B8H8As2Se in low yield. Reaction of B7C2H13 with potassium polyselenide gave the arachno selenacarborane B7H2C11Se in low yield. The structure of the new heteroborane is proposed on the basis of 11B and 1H nmr spectra. Reaction of B7C2H13 with AsCl3 resulted in the isolation of white stable crystals of B7C2H9As2 in 40 percent yield

  17. Inhibition of pH fronts in corrosion cells due to the formation of cerium hydroxide

    International Nuclear Information System (INIS)

    The effect of cerium-based corrosion inhibitors on the pH front between the alkaline cathode and acidic anode in corrosion cells has been studied. The cerium component of these inhibitors can affect the pH front since it precipitates in an alkaline environment as cerium hydroxide, which is important since the corrosion inhibition mechanism of the cerium component is a result of its deposition as a highly electrical resistive (passivation) layer on the cathode. It is studied whether the cerium can reach the cathode when fed into the corrosion cell from an external source after the onset of corrosion. To this end a simulation model was set up that includes the Poisson–Nernst–Planck theory to describe ion transport and the Frumkin–Butler–Volmer equation to describe charge transfer at the electrodes. In this model both the self-dissociation of water and the formation of cerium hydroxide are taken into account. To support our findings experimentally a corrosion cell consisting of an aluminum and copper electrode was used, in which the pH fronts were visualized using a pH-indicator. Two types of inhibitors were used; namely, highly soluble CeCl3 and sparsely soluble cerium dibutylphosphate, Ce(dbp)3. The results show that CeCl3 can reduce the size of the alkaline region and reach the cathode to form a passivation layer, whereas the solubility in case of Ce(dbp)3 is too low to supply sufficient amounts of trivalent cerium cations to penetrate the alkaline region. This behavior can be explained by the simulation results, which reveal a threshold for the corrosion inhibitor solubility below which no passivation of the cathode occurs

  18. Construction of heterocyclic structures by trivalent cerium salts promoted bond forming reactions.

    Science.gov (United States)

    Properzi, Roberta; Marcantoni, Enrico

    2014-02-01

    Cerium(III) salts have recently gained increasing attention in the synthetic community, owing to the powerful features that are reviewed in detail in this tutorial. This review reports significant examples of cerium(III) promoted synthesis of heterocyclic structures, initially dealing with the synthesis of five- and six-membered ring nitrogen containing heterocycles, then describing the preparation of their oxygenated analogues and finally discussing the achievement of seven-membered rings and mixed heterocyclic motifs. PMID:24217370

  19. Protein adsorption and cellular uptake of cerium oxide nanoparticles as a function of zeta potential

    OpenAIRE

    Patil, Swanand; Sandberg, Amanda; Heckert, Eric; Self, William; Seal, Sudipta

    2007-01-01

    The surface chemistry of biomaterials can have a significant impact on their performance in biological applications. Our recent work suggests that cerium oxide nanoparticles are potent antioxidants in cell culture models and we have evaluated several therapeutic applications of these nanoparticles in different biological systems. Knowledge of protein adsorption and cellular uptake will be very useful in improving the beneficial effects of cerium oxide nanoparticles in biology. In the present ...

  20. Effects of Morphology of Cerium Oxide Catalysts for Reverse Water Gas Shift Reaction

    OpenAIRE

    Kovasevic, M.; Mojet, B.L.; Ommen, van, B.; Lefferts, L.

    2016-01-01

    Reverse water gas shift reaction (RWGS) was investigated over cerium oxide catalysts of distinct morphologies: cubes, rods and particles. Catalysts were characterized by X-ray diffraction, Raman spectroscopy and temperature programmed reduction (TPR) in hydrogen. Nanoshapes with high concentration of oxygen vacancies contain less surface oxygen removable in TPR. Cerium oxide cubes exhibited two times higher activity per surface area as compared to rods and particles. Catalytic activity of the...

  1. Catalysts with Cerium in a Membrane Reactor for the Removal of Formaldehyde Pollutant from Water Effluents

    OpenAIRE

    Mirella Gutiérrez-Arzaluz; Luis Noreña-Franco; Saúl Ángel-Cuevas; Violeta Mugica-Álvarez; Miguel Torres-Rodríguez

    2016-01-01

    We report the synthesis of cerium oxide, cobalt oxide, mixed cerium, and cobalt oxides and a Ce–Co/Al2O3 membrane, which are employed as catalysts for the catalytic wet oxidation (CWO) reaction process and the removal of formaldehyde from industrial effluents. Formaldehyde is present in numerous waste streams from the chemical industry in a concentration low enough to make its recovery not economically justified but high enough to create an environmental hazard. Common biological degradation ...

  2. Energy-dispersive X-ray fluorescence analysis of cerium in ferrosilicon

    International Nuclear Information System (INIS)

    The cerium was determined in ferrosilicon samples by energy-dispersive X-ray fluorescence techniques (XRF) techniques, with a secondary target of gadolinium. The methods employed were: comparison and linear regression with reference materials with cerium concentration between 0.4 and 1.0%. The samples were prepared in the form of pellets and the analytical results are reported as an average of five determinations with a confidence limits at 95% probability. (Author)

  3. Imidazolium ionic liquids as solvents for cerium(IV)-mediated oxidation reactions

    OpenAIRE

    Mehdi, Hasan; Bodor, Andrea; Lantos, Diana; Horváth, István T; De Vos, Dirk; Binnemans, Koen

    2007-01-01

    Use of imidazolium ionic liquids as solvents for organic transformations with tetravalent cerium salts as oxidizing agents was evaluated. Good solubility was found for ammonium hexanitratocerate(IV) (ceric ammonium nitrate, CAN) and cerium(IV) triflate in 1-alkyl-3-methylimidazolium triflate ionic liquids. Oxidation of benzyl alcohol to benzaldehyde in 1-ethyl-3-methylimidazolium triflate was studied by in-situ FTIR spectroscopy and 13C NMR spectroscopy on carbon-13-labeled benzyl alcohol. Ca...

  4. Uranium Hydride Nucleation Kinetics: Effects of Oxide Thickness and Vacuum Outgassing

    International Nuclear Information System (INIS)

    Many factors such as impurities in the oxide and metal, microstructure, gas impurities, and oxide thickness may influence the rate and location of the nucleation of hydride on uranium. This work has concentrated on isolating one of these variables, the oxide thickness, and measuring the effect of the oxide thickness on uranium hydride nucleation. Uranium samples, all from the same lot, were prepared with different oxide thicknesses. The oxide thickness was measured using Rutherford Backscattering Spectroscopy. Oxidized uranium samples were then exposed to ultra-high purity hydrogen gas under constant volume conditions. Decreases in pressure indicated hydrogen uptake by the sample. The time for hydride nucleation--as well as the maximum hydriding rate--was then calculated from the measured decreases in pressure. The time to nucleate a hydride was found to increase whereas the maximum hydriding rate was found to decrease with increasing oxide thickness. The density of hydride pits also decreased with increasing oxide thickness. The observed results support the argument that the nucleation of hydride is controlled somewhat by diffusion of hydrogen through the oxide layer. Vacuum outgassing of samples, thereby removing the oxide impurities and keeping the oxide thickness constant, dramatically decreased the nucleation time and increased the maximum hydriding rate. Again, this is consistent with hydrogen diffusion through the oxide controlling the nucleation of hydride. Impurities in the oxide layer can decrease the diffusivity of hydrogen and therefore delay the nucleation of uranium hydride

  5. A chemical cleaning process with Cerium (IV)-sulfuric acid

    International Nuclear Information System (INIS)

    A chemical cleaning process with a high decontamination factor (DF) is requested for decommissioning. Usually, the process should be qualified with the features, such as the feasibility of treating large or complicated form waste, the minimization of secondary waste. Therefore, a powerful technique of redox decontamination process with Ce+4/Ce+3 has been studied at INER. First, the redox of cerium ion with electrolytic method was developed. Two kinds of home-made electrolyzer were used. One is with an ion-exchange membrane, and the other one is with a ceramic separator. Second, factors influencing the decontamination efficiency, such as the concentration of Ce+4, regeneration current density, temperature, acidity of solution were all studied experimentally, and the optimum conditions were specified too. Third, the liquid waste recycling and treatment were developed with electrodialysis and ion-exchange absorption methods. Finally, the hot test was proceeded with the contaminated metals from DCR of nuclear facility. (author)

  6. Extraction behavior of cerium by tetraoctyldiglycolamide from nitric acid solutions

    International Nuclear Information System (INIS)

    The diamide N,N,N',N'-tetraoctyldiglycolamide (TODGA) was synthesized and characterized. The prepared TODGA was applied for extraction of Ce(III) from nitric acid solutions. The equilibrium studies included the dependencies of cerium distribution ratio on nitric acid, TODGA, nitrate ion, hydrogen ion and cerous ion concentrations. Analysis of the results indicates that the main extracted species is Ce(TODGA)2(NO3)3HNO3. The capacity of Ce loading is approximately 45 mmol/L for 0.1 M solution of TODGA in n-hexane. Finally, the thermodynamic parameters were calculated: K (25 deg C) = 3.8 x 103, ΔH = -36.7 ± 1.0 kJ/mol, ΔS = -54.6 ± 3.0 J/K mol, and ΔG = -20.4 ± 0.1 kJ/mol. (author)

  7. Deposition and investigation of lanthanum cerium hexaboride thin films

    Science.gov (United States)

    Kuzanyan, A. S.; Harutyunyan, S. R.; Vardanyan, V. O.; Badalyan, G. R.; Petrosyan, V. A.; Kuzanyan, V. S.; Petrosyan, S. I.; Karapetyan, V. E.; Wood, K. S.; Wu, H.-D.; Gulian, A. M.

    2006-09-01

    Thin films of lanthanum-cerium hexaboride, the promising thermoelectric material for low-temperature applications, are deposited on various substrates by the electron-beam evaporation, pulsed laser deposition and magnetron sputtering. The influence of the deposition conditions on the films X-ray characteristics, composition, microstructure and physical properties, such as the resistivity and Seebeck coefficient, is studied. The preferred (100) orientation of all films is obtained from XRD traces. In the range of 780-800 °C deposition temperature the highest intensity of diffractions peaks and the highest degree of the preferred orientation are observed. The temperature dependence of the resistivity and the Seebeck coefficient of films are investigated in the temperature range of 4-300 K. The features appropriate to Kondo effect in the dependences ρ( T) and S( T) are detected at temperatures below 20 K. Interplay between the value of the Seebeck coefficient, metallic parameters and Kondo scattering of investigated films is discussed.

  8. Structure and activity of tellurium-cerium oxide acrylonitrile catalysts

    International Nuclear Information System (INIS)

    Ammoxidation of propylene to acrylonitrile (ACN) was investigated over various silica-supported (Te,Ce)O catalysts at 360 and 4400C. The binary oxide system used consists of a single nonstoichiometric fluorite-type phase α-(Ce,Te)O2 up to about 80 mole% TeO2 and a tellurium-saturated solid solution β-(Ce,Te)O2 at higher tellurium concentrations. The ACN yield varies almost linearly with the tellurium content of (Ce,Te)O2. The β-(Ce,Te)O2 phase is the most active component of the system (propylene conversion and ACN selectivity at 440 C of 76.7 and 74%, respectively) and is slightly more selective to ACN than α-Te02. Tellurium reduces the overoxidation properties of cerium and selective oxidation occurs through Te(IV)-bonded oxygen

  9. Effect of Surface Modification on Behaviors of Cerium Oxide Nanopowders

    Institute of Scientific and Technical Information of China (English)

    Li Mei; Shi Zhenxue; Liu Zhaogang; Hu Yanhong; Wang Mitang; Li Hangquan

    2007-01-01

    Study was made on the effect of surface modification on the behaviors of cerium oxide nanopowders. A surfactant-sodium dodecyl sulfate(C12H25SO4Na) was used to modify the surface of CeO2 powder particles. The unmodified and modified CeO2 powders were characterized by using a powder comprehensive characteristic tester, laser particle size analyzer, specific surface area tester, X-ray diffraction tester, and a scanning electron microscope. The testing and analysis results showed that C12H25SO4Na surface modification might increase the flowability and dispersity, and decrease the specific surface area and agglomeration of CeO2 powders. The mechanism of the surface modification of CeO2 powder particles was also discussed.

  10. Management of decontamination solution arising from Cerium redox process

    International Nuclear Information System (INIS)

    This paper describes the recovery of Pu from decontamination stream generated from Cerium Redox Process meant for decontamination of contaminated metallic wastes. Extraction of Pu is carried out using PUREX solvent after reducing it to tetravalent state which is subsequently stripped using hydroxylamine nitrate and nitric acid mixture. Raffinate from this step containing Ce3+, 241Am and corrosion products is subjected to ozonisation wherein Ce3+ is oxidized to Ce4+. Quantitative extraction of Ce is achieved by PUREX solvent in second cycle which is stripped using a mixture of NaNO2 and HNO3. Raffinate from this step contains 241Am and corrosion product which is removed by solvent extraction using TEHDGA. The final alpha lean waste can be managed by cementation. (author)

  11. Modification mechanism of cerium on the Al-18Si alloy

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The effect of the rare earth cerium (Ce) on the hypereutectic Al-Si alloy under different casting states have been studied by optical microscope and quantitative image analysis. It is found that the size and the quantity of primary silicon in castings decrease with the increase of added Ce in the melt. Meanwhile primary silicon changes from branched shape to fine facetted shape. Although the modification on eutectic silicon in castings also improves with the increase of added Ce in the melt, the effect of modification on eutectic silicon away from primary silicon is more obvious than that on eutectic silicon close to primary silicon. The modification mechanism was analyzed in detail by means of scanning electron microscope equipped with energy dispersive analysis of X-ray and thermodynamics analysis, which included the analysis on the change in standard Gibbs energy of reaction and reaction equilibrium.

  12. Internal friction study of hydrides in zirconium at low hydrogen contents

    International Nuclear Information System (INIS)

    Full text: Internal friction and shear modulus measurements were carried out on crystal bar zirconium in the as received and hydride conditions using an inverted forced pendulum. Hydriding was achieved in two ways: inside and out of the pendulum. The final hydrogen content determined by fusion analysis in the 'in situ' hydride sample was of 36 ppm. Another sample was hydride by the cathodic charge method with 25 ppm. The thermal solid solubility (TSS) phase boundary presents hysteresis between the precipitation (TSSP) and the dissolution (TSSD) temperatures for the zirconium hydrides. During the first thermal cycling the anelastic effects could be attributed to the δ, ε and metastable γ zirconium hydrides. After 'in situ' annealing at 490 K, these peaks completely disappear in the electrolytically charged sample, while in the 'in situ' hydride, the peaks remain with decreasing intensity. This effect can be understood in terms of the different surface conditions of the samples. (author)

  13. Comparison of irradiation hardening and microstructure evolution in ion-irradiated delta and epsilon hydrides

    Energy Technology Data Exchange (ETDEWEB)

    Oono, Naoko, E-mail: n-oono@eng.hokudai.ac.jp [Institute of Advanced Energy, Kyoto University, Gokasho, Uji, Kyoto 611-0011 (Japan); Kasada, Ryuta [Institute of Advanced Energy, Kyoto University, Gokasho, Uji, Kyoto 611-0011 (Japan); Higuchi, Toru; Sakamoto, Kan; Nakatsuka, Masafumi [Nippon Nuclear Fuel Development Co., Ltd., 2163 Naritacho Oarai, Higashi-Ibaraki, Ibaraki 311-1313 (Japan); Hasegawa, Akiko; Kondo, Sosuke; Iwata, Noriyuki Y.; Matsui, Hideki; Kimura, Akihiko [Institute of Advanced Energy, Kyoto University, Gokasho, Uji, Kyoto 611-0011 (Japan)

    2013-11-15

    A δ-Zr-hydride was irradiated with 6.4 MeV Fe{sup 3+} ions to clarify the relationship between hardening and microstructural changes of bulk Zr-hydrides under neutron irradiation. Irradiation hardening was measured by nanoindentation tests. Transmission electron microscope cross-sectional observations showed that the deformation mechanism of the δ-Zr-hydride was both slip and twinning. Dislocation loops were observed in the irradiated hydride matrix. These irradiation-induced defects make slip deformation difficult and consequently promote the twin deformation of δ-Zr-hydride. This work is a continuation of the previous our work (J. Nucl. Mater. 419 (2011) 366–370) focused upon ε-Zr-hydride and we discuss a comparison between the two Zr-hydrides.

  14. Mechanochemical synthesis and spark plasma sintering of the cerium silicides

    International Nuclear Information System (INIS)

    Highlights: • Ce5Si3, Ce3Si2, CeSi, CeSi2−x and CeSi2 were mechanochemically synthesized. • Temperature and pressure were monitored to investigate reaction progress. • All syntheses proceeded through a MSR event followed by rapid solid-state diffusion. • Milling time before MSR correlates well with effective heat of formation. • Some synthesized material was densified by spark plasma sintering. - Abstract: The cerium silicides, Ce5Si3, Ce3Si2, CeSi, CeSi2−y, and CeSi2−x, have been prepared from the elements by mechanochemical processing in a planetary ball mill. Preparation of the cerium silicide Ce5Si4 was unsuccessfully attempted and potential reasons for this are discussed. Temperature and pressure of the milling vial were monitored in situ to gain insight into the mechanochemical reaction kinetics, which include a mechanically-induced self-propagating reaction (MSR). Some prepared powders were consolidated by spark plasma sintering to high density. Starting materials, as-milled powders, and consolidated samples were characterized by X-ray diffraction, scanning electron microscopy, and energy dispersive spectroscopy. The results obtained help elucidate key questions in mechanochemical processing of intermetallics, showing first phase formation similar to thin films, MSR ignition times that are composition- and milling speed-dependent, and sensitivity of stable compound formation on the impact pressure. The results demonstrate mechanochemical synthesis as a viable technique for rare earth silicides

  15. Mechanochemical synthesis and spark plasma sintering of the cerium silicides

    Energy Technology Data Exchange (ETDEWEB)

    Alanko, Gordon A.; Jaques, Brian; Bateman, Allyssa [Department of Materials Science and Engineering, College of Engineering, Boise State University, 1910 University Drive, Boise, ID 83725 (United States); Butt, Darryl P., E-mail: darrylbutt@boisestate.edu [Department of Materials Science and Engineering, College of Engineering, Boise State University, 1910 University Drive, Boise, ID 83725 (United States); Center for Advanced Energy Studies, 995 University Boulevard, Idaho Falls, ID 83401 (United States)

    2014-12-15

    Highlights: • Ce{sub 5}Si{sub 3}, Ce{sub 3}Si{sub 2}, CeSi, CeSi{sub 2−x} and CeSi{sub 2} were mechanochemically synthesized. • Temperature and pressure were monitored to investigate reaction progress. • All syntheses proceeded through a MSR event followed by rapid solid-state diffusion. • Milling time before MSR correlates well with effective heat of formation. • Some synthesized material was densified by spark plasma sintering. - Abstract: The cerium silicides, Ce{sub 5}Si{sub 3}, Ce{sub 3}Si{sub 2}, CeSi, CeSi{sub 2−y}, and CeSi{sub 2−x}, have been prepared from the elements by mechanochemical processing in a planetary ball mill. Preparation of the cerium silicide Ce{sub 5}Si{sub 4} was unsuccessfully attempted and potential reasons for this are discussed. Temperature and pressure of the milling vial were monitored in situ to gain insight into the mechanochemical reaction kinetics, which include a mechanically-induced self-propagating reaction (MSR). Some prepared powders were consolidated by spark plasma sintering to high density. Starting materials, as-milled powders, and consolidated samples were characterized by X-ray diffraction, scanning electron microscopy, and energy dispersive spectroscopy. The results obtained help elucidate key questions in mechanochemical processing of intermetallics, showing first phase formation similar to thin films, MSR ignition times that are composition- and milling speed-dependent, and sensitivity of stable compound formation on the impact pressure. The results demonstrate mechanochemical synthesis as a viable technique for rare earth silicides.

  16. Cooling Performance Improvement of the Heat Driven Type Metal Hydride Refrigerator-Heat Transfer Enhancement Influence of Metal Hydride Sheet Loading Into a Metal Hydride Particle Bed

    OpenAIRE

    Bae, Sangchul; Katsuta, Masafumi; Homma, Ikuto; Morita, Eiji

    2012-01-01

    In the refrigeration and air conditioning fields, the demands of energy conservation and renewable energy have been increased recently. In this study, we aim at the development of the heat driven type metal hydride (abbr., MH) that can be driven by the low temperature exhaust or solar heat under 100ᵒC. In order to use this system commercially, heat transfer enhancement of MH particle bed, activation characteric improvement and production cost reduction of MH must be achieved. In this study, w...

  17. Study on the uranium-cerium extraction and his application to the treatment of irradiated uranium

    International Nuclear Information System (INIS)

    It was made a study on the behavior of uranium and cerium(IV) extraction, using the latter element as a plutonium simulator in a flowsheet of the treatment of irradiated uranium. Cerium(IV) was used under the same conditions as a plutonium in the Purex process because the admitted similar properties. An experimental work was initiated to determine the equilibrium curves of uranium, under the following conditions: concentration of 1 to 20 g U/1 and acidity varying from 1 to 5M in HNO3. Other parameters studied were the volumetric ratio of the phases and the influence of the concentration of TBP (tri-n-butyl phosphate). To guarantee the cerium(IV) extraction, the diluent (varsol) was previously treated with 10% potassium dichromate in perchloric acid, potassium permanganate in 1M sulphuric acid and concentrated sulphuric acid at 70 deg to eliminate reducing compounds. The results obtained for cerium extraction, allowed a better understanding of its behavior in solution. The results permitted to conclude that the decontamination for cerium are very high in the first Purex extraction cycle. The easy as cerium(IV) is reduced to the trivalent state contributes a great deal to its decontamination. (author)

  18. Extraction of tetravalent berkelium and cerium by aliquate-336-S-NO3 quaternary ammonium salt

    International Nuclear Information System (INIS)

    Extraction of tetravalent berkelium and cerium by aliquate-336-S-NO3 quaternary ammonium salt from nitric acid solutions is investigated. The effect of concentrations of nitric acid and extracting agent, nature of an oxidant (potassium bromate, potassium bichromate, mixture of AgNO3 and (NH4)2S2O8) and solvent on the distribution coefficient of berkelium(4) and cerium(4) is studied. It is established that solutions of aliquate-336-S-NO3 in carbon tetrachloride and dichloroethane extract quantitatively tetravalent berkelium from 10-12 M nitric acid solutions and cerium - from 1-10 M nitric acid solutions containing potassium bichromate as an oxidant. It is shown that the value of distribution coefficient for berkelium and cerium depends on the nature of an oxidant and extracting agent concentration. It is established that in the case of extraction by quaternary ammonium salt with one berkelium(4) mole four aliquate-336-SNO3 moles are associated and 1.5-1.6 mole of extracting agent are associated with one cerium(4) mole. It permits to make a conclusion that stoichiometry of extraction reactions by quaternary ammonium salt is not the same for tetravalent berkelium and cerium. It is shown that trivalent transplutonium and rare earth elements are not practically extracted by aliquate-336-S-NO3 from nitric acid solutions

  19. Electrochromism of Mg-Ni hydride switchable mirrors

    Science.gov (United States)

    Isidorsson, Jan; Giebels, I. A. M. E.; Di Vece, M.; Griessen, Ronald

    2001-11-01

    Switchable mirrors have so far been made of rare-earth and rare-earth-magnesium based metal-hydrides. In this investigation we study Mg-Ni-hydrides, which have been shown by Richardson et al. to exhibit switchable properties similar to those of the rare-earth hydrides. Cyclic voltammetry on MgzNiHx samples with 0.8 less than z less than 3.7 shows that addition of one Mg atom per Mg2Ni gives the best ab/desorption kinetics for hydrogen. X- ray diffraction reveals a structural change as hydrogen is absorbed. The metal-insulator transition is confirmed with simultaneous resistivity measurements. A pressure- composition isotherm of Mg2NiHx is also determined electrochemically. Optical spectrometry during gas loading gives an optical band gap of 1.6 eV for Mg2NiH4. This gap increases with increasing Mg content in a way similar to that of the Mg-doped rare-earth hydrides.

  20. Structural deformation of metallic uranium surrounding hydride growth sites

    International Nuclear Information System (INIS)

    Highlights: • UH3 formation on uranium surfaces by a controlled uptake of hydrogen at 240 °C. • Large hydride growths (35–125 μm in diameter) form at the surface. • Confined hydride expansion during growth generates stress in the subsurface. • EBSD scans found micro-cracking and twins as forms of stress relief in the metal. - Abstract: Electron backscatter diffraction (EBSD) was utilised to probe the microstructure of uranium metal in the vicinity of surface corrosion pits, resulting from hydrogen exposure (5 × 104 Pa, at 240 °C). Microstructural analysis of the surface revealed a subtle increase of grain orientation variation for grains at the border of the hydride growths. Cross sectional analysis, at pit sites, revealed significant microstructure deformation in the form of crystal twinning and micro-cracking beneath the surface. These observations provide qualitative evidence that local stress intensities generated as a consequence of hydride growth and confinement, were sufficient to cause deformation within the parent metal

  1. Design and integration of a hydrogen storage on metallic hydrides

    International Nuclear Information System (INIS)

    This work presents a hydrogen storage system using metal hydrides for a Combined Heat and Power (CHP) system. Hydride storage technology has been chosen due to project specifications: high volumetric capacity, low pressures (≤ 3.5 bar) and low temperatures (≤ 75 C: fuel cell temperature). During absorption, heat from hydride generation is dissipated by fluid circulation. An integrated plate-fin type heat exchanger has been designed to obtain good compactness and to reach high absorption/desorption rates. At first, the storage system has been tested in accordance with project specifications (absorption 3.5 bar, desorption 1.5 bar). Then, the hydrogen charge/discharge times have been decreased to reach system limits. System design has been used to simulate thermal and mass comportment of the storage tank. The model is based on the software Fluent. We take in consideration heat and mass transfers in the porous media during absorption/desorption. The hydride thermal and mass behaviour has been integrated in the software. The heat and mass transfers experimentally obtained have been compared to results calculated by the model. The influence of experimental and numerical parameters on the model behaviour has also been explored. (author)

  2. Nanocrystalline Metal Hydrides Obtained by Severe Plastic Deformations

    Directory of Open Access Journals (Sweden)

    Jacques Huot

    2012-01-01

    Full Text Available It has recently been shown that Severe Plastic Deformation (SPD techniques could be used to obtain nanostructured metal hydrides with enhanced hydrogen sorption properties. In this paper we review the different SPD techniques used on metal hydrides and present some specific cases of the effect of cold rolling on the hydrogen storage properties and crystal structure of various types of metal hydrides such as magnesium-based alloys and body centered cubic (BCC alloys. Results show that generally cold rolling is as effective as ball milling to enhance hydrogen sorption kinetics. However, for some alloys such as TiV0.9Mn1.1 alloy ball milling and cold rolling have detrimental effect on hydrogen capacity. The exact mechanism responsible for the change in hydrogenation properties may not be the same for ball milling and cold rolling. Nevertheless, particle size reduction and texture seems to play a leading role in the hydrogen sorption enhancement of cold rolled metal hydrides.

  3. Study on the effect of hydrogen purification with metal hydride

    International Nuclear Information System (INIS)

    The effects of hydrogen purification with a AB5-type metal hydride were studied for the development of hydrogen purification system. The system set up two packed-beds, heat exchangers, data acquisition equipment and automatic control unit was used in the work and the compositions of two different gas-mixtures have CO, CH4, CO2, O2 and N2. We investigated about its tolerance against impurities, pressure-composition-isotherm and life cycle test, XRD and particle size analysis with a used metal hydride. Gas chromatograph was used for the analysis of feed and product gas. The used metal hydride is a La, Nd-rich Mm-based AB5 type which has the hydrogen storage capacity of 1.4 wt%. In life cycle test, there were no change of plateau pressure and hysteresis after 600 cycles but hydrogen storage capacity was decreased by about 6.8% and 10.7% after 220, 600 cycles, respectively. The used sample is high strong against CH4 and CO2 but very weak in CO atmosphere. The hydrogen purification performance with gas mixtures was decreased in the order of CH4 ≥ CO ≥ O2 ≥ N2 ≥ CO2. The reason CO investigated high purification effect in gas mixture is due to a strong chemisorption in metal hydride matrix that CO was not released out of the alloy. (authors)

  4. Hydrogen adsorption on palladium and palladium hydride at 1 bar

    DEFF Research Database (Denmark)

    Johansson, Martin; Skulason, Egill; Nielsen, Gunver;

    2010-01-01

    The dissociative sticking probability for H-2 on Pd films supported on sputtered Highly Ordered Pyrolytic Graphite (HOPG) has been derived from measurements of the rate of the H-D exchange reaction at 1 bar. The sticking probability for H-2, S. is higher on Pd hydride than on Pd (a factor of 1.4 ...

  5. Process of forming a sol-gel/metal hydride composite

    Science.gov (United States)

    Congdon, James W.

    2009-03-17

    An external gelation process is described which produces granules of metal hydride particles contained within a sol-gel matrix. The resulting granules are dimensionally stable and are useful for applications such as hydrogen separation and hydrogen purification. An additional coating technique for strengthening the granules is also provided.

  6. Thin-film metal hydrides for solar energy applications

    Energy Technology Data Exchange (ETDEWEB)

    Mongstad, Trygve Tveiteraas

    2012-11-01

    Thin-film metal hydrides may become important solar energy materials in the future. This thesis demonstrates interesting material properties of metal hydride films, relevant for applications as semiconducting materials for photovoltaic (PV) solar cells and for regulation of light using smart window technology.The work presented here has comprised an experimental study, focusing on three different materials: Magnesium hydride (MgH2), magnesium nickel hydride (Mg2NiH4) and yttrium hydride (YHx). Reactive sputter deposition was used to prepare the metal hydride film samples.This synthesis method is relatively uncommon for metal hydrides. Here,the first demonstration of reactive sputtering synthesis for YHx and Mg2NiH4 is given. Different challenges in forming singlephase, pure metal hydrides were identified: MgH2 could not be deposited without 3-16% metallic Mg present in the films, and YHx was found to react strong-ly to oxygen (O) during the deposition process. On the other hand, Mg2NiH4 films formed easily and apparently without major metallic clusters and with low O content.Mg2NiH4 is a semiconductor with an optical band gap that is suitable for PV solar cells. This study has showed that films with promising electrical and optical properties can be synthesized using reactive cosputtering of Mg and Ni. Using optical methods, the band gap for the as deposited samples was estimated to 1.54-1.76 eV, depending on the Mg-Ni composition. The asdeposited films were amorphous or nano-crystalline, but could be crystallized into the high-temperature fcc structure of Mg2NiH4 using heat treatment at 523 K. The band gap of the crystalline films was 2.1-2.2 eV, depending on the composition.A pronounced photochromic reaction to visible and UV light was observed for transparent yttrium hydride (T-YHx) samples. The optical transmission was reduced when the samples were illuminated, and the original optical transmission was restored when the samples were kept under dark conditions

  7. Synthesis of hydrides by interaction of intermetallic compounds with ammonia

    Energy Technology Data Exchange (ETDEWEB)

    Tarasov, Boris P., E-mail: tarasov@icp.ac.ru [Institute of Problems of Chemical Physics of the Russian Academy of Sciences, Chernogolovka 142432 (Russian Federation); Fokin, Valentin N.; Fokina, Evelina E. [Institute of Problems of Chemical Physics of the Russian Academy of Sciences, Chernogolovka 142432 (Russian Federation); Yartys, Volodymyr A., E-mail: volodymyr.yartys@ife.no [Institute for Energy Technology, Kjeller NO 2027 (Norway); Department of Materials Science and Engineering, Norwegian University of Science and Technology, Trondheim NO 7491 (Norway)

    2015-10-05

    Highlights: • Interaction of the intermetallics A{sub 2}B, AB, AB{sub 2}, AB{sub 5} and A{sub 2}B{sub 17} with NH{sub 3} was studied. • The mechanism of interaction of the alloys with ammonia is temperature-dependent. • Hydrides, hydridonitrides, disproportionation products or metal–N–H compounds are formed. • NH{sub 4}Cl was used as an activator of the reaction between ammonia and intermetallics. • Interaction with ammonia results in the synthesis of the nanopowders. - Abstract: Interaction of intermetallic compounds with ammonia was studied as a processing route to synthesize hydrides and hydridonitrides of intermetallic compounds having various stoichiometries and types of crystal structures, including A{sub 2}B, AB, AB{sub 2}, AB{sub 5} and A{sub 2}B{sub 17} (A = Mg, Ti, Zr, Sc, Nd, Sm; B = transition metals, including Fe, Co, Ni, Ti and nontransition elements, Al and B). In presence of NH{sub 4}Cl used as an activator of the reaction between ammonia and intermetallic alloys, their interaction proceeds at rather mild P–T conditions, at temperatures 100–200 °C and at pressures of 0.6–0.8 MPa. The mechanism of interaction of the alloys with ammonia appears to be temperature-dependent and, following a rise of the interaction temperature, it leads to the formation of interstitial hydrides; interstitial hydridonitrides; disproportionation products (binary hydride; new intermetallic hydrides and binary nitrides) or new metal–nitrogen–hydrogen compounds like magnesium amide Mg(NH{sub 2}){sub 2}. The interaction results in the synthesis of the nanopowders where hydrogen and nitrogen atoms become incorporated into the crystal lattices of the intermetallic alloys. The nitrogenated materials have the smallest particle size, down to 40 nm, and a specific surface area close to 20 m{sup 2}/g.

  8. Synthesis and enhanced hydrogen desorption kinetics of magnesium hydride using hydriding chemical vapor synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Jin-Ho [Icheon Branch, Korea Institute of Ceramic Engineering and Technology (KICET), Icheon-si, Gyeonggi-do (Korea, Republic of); Kim, Byung-Goan [Korea Energy Materials Co.Ltd., 409, Daegu Technopark, 1-11, Hosan-Dong, Dalse-Gu 704-230 (Korea, Republic of); Kang, Yong-Mook, E-mail: dake@kaist.ac.kr [Department of Chemistry, Dongguk University-Seoul, 100715 Seoul (Korea, Republic of)

    2012-07-15

    Highlights: Black-Right-Pointing-Pointer We synthesized pure MgH{sub 2} by a hydriding chemical vapor synthesis process in a hydrogen atmosphere. Black-Right-Pointing-Pointer The particle size HCVS-MgH{sub 2} was drastically reduced to the sub-micron or micrometer-scale. Black-Right-Pointing-Pointer HCVS-MgH{sub 2} showed different shapes (needle-like nanofibers and angulated plate) depending on the deposited position. Black-Right-Pointing-Pointer HCVS-MgH{sub 2} desorbed hydrogen up to about 7.2 wt% and 7.1 wt%. - Abstract: This paper describes the hydriding chemical vapor synthesis (HCVS) of the hydrogen storage alloy MgH{sub 2} in a hydrogen atmosphere and the product's hydrogenation properties. Mg powder was used as a starting material to produce submicron MgH{sub 2} and uniformly heated to a temperature of 600 Degree-Sign C for Mg vaporization. The effects of deposited positions in HCVS reactor on the morphology and the composition of the obtained products were examined by using X-ray diffraction (XRD), scanning electron microscopy (SEM), and Brunauer-Emmett-Teller (BET) analyses. It is clearly seen that after the HCVS process, the particle size of synthesized MgH{sub 2} was drastically reduced to the sub-micron or micrometer-scale and these showed different shapes (needle-like nanofibers and angulated plate) depending on the deposited position. The hydrogen desorption temperatures of HCVS-MgH{sub 2} were measured using a differential scanning calorimeter (DSC). It was found that after the HCVS process, the desorption temperature of HCVS-MgH{sub 2} decreased from 430 to 385 Degree-Sign C and, simultaneously, the smallest particle size and the highest specific surface area were obtained. These observations indicate that the minimum hydrogen desorption temperature of HCVS-MgH{sub 2} powder with needle-like form can be obtained, and that this temperature is dependent on the particle size and the specific surface area of the products. The thermogravimetric

  9. Exploring metal hydrides using autoclave and multi-anvil hydrogenations

    Science.gov (United States)

    Puhakainen, Kati

    Metal hydride materials have been intensively studied for hydrogen storage applications. In addition to potential hydrogen economy applications, metal hydrides offer a wide variety of other interesting properties. For example, hydrogen-dominant materials, which are hydrides with the highest hydrogen content for a particular metal/semimetal composition, are predicted to display high-temperature superconductivity. On the other side of the spectrum are hydrides with small amounts of hydrogen (0.1 - 1 at.%) that are investigated as viable magnetic, thermoelectric or semiconducting materials. Research of metal hydride materials is generally important to gain fundamental understanding of metal-hydrogen interactions in materials. Hydrogenation of Zintl phases, which are defined as compounds between an active metal (alkali, alkaline earth, rare earth) and a p-block metal/semimetal, were attempted by a hot sintering method utilizing an autoclave loaded with gaseous hydrogen (Hydride formation competes with oxidative decomposition of a Zintl phase. The oxidative decomposition, which leads to a mixture of binary active metal hydride and p-block element, was observed for investigated aluminum (Al) and gallium (Ga) containing Zintl phases. However, a new phase Li2Al was discovered when Zintl phase precursors were synthesized. Using the single crystal x-ray diffraction (SCXRD), the Li2Al was found to crystallize in an orthorhombic unit cell (Cmcm) with the lattice parameters a = 4.6404(8) Å, b = 9.719(2) Å, and c = 4.4764(8) Å. Increased demand for materials with improved properties necessitates the exploration of alternative synthesis methods. Conventional metal hydride synthesis methods, like ball-milling and autoclave technique, are not responding to the demands of finding new materials. A viable alternative synthesis method is the application of high pressure for the preparation of hydrogen-dominant materials. Extreme pressures in the gigapascal ranges can open access to

  10. Hydride redistribution and crack growth in Zr-2.5 wt.% Nb stressed in torsion

    International Nuclear Information System (INIS)

    The effect of applied shear stresses on zirconium hydride solubility in a zirconium alloy was investigated. Recent studies have shown that zirconium hydride precipiates probably nucleate and grow by means of a shear transformation mechanism. It is postulated that these transformation shear strains can interact with applied shear stress gradients in the same way that the dilatational strains can interact with a dilatational stress gradient, providing a driving force for hydride accumulation, hydride embrittlement and crack propagation. To test this proposition, crack growth experiments were carried out under torsional loading conditions on hydrided, round notched bar specimens of cold-worked Zr-2.5 wt.% Nb cut from Pickering-type pressure tube material. Postmortem metallographic examination of the hydride distribution in these samples showed that, in many cases, the hydrides appeared to have reoriented in response to the applied shear stress and that hydride accumulation at the notch tip had occurred. However, except in a few cases, the rate of accumulation of reoriented hydrides at the notch tip due to applied shear stresses was much less than the rate due to corresponding applied uniaxial stresss. Moreover, the process in shear appears to be more sensitive to the inital hydride size. Attempts to elucidate the fracture mechanism by fractographic examination using scanning and replica transmission electron microscopy proved to be inconclusive because of smearing of the fracture face. (auth)

  11. Metal Hydride Wall Stress Measurements on a Four-Inch Short (FISH) Bed

    International Nuclear Information System (INIS)

    A 38 cm (15 inch) long metal hydride bed fabricated using 11.4 cm (4.5 inch) O.D., standard schedule 316/316L stainless steel pipe was fitted with 22 strain gauges to measure tangential and longitudinal stress resulting from hydride absorption and desorption cycling. Tests were conducted using two different LaNi4.25Al0.75 metal hydride fill-levels in the bed.Tests conducted with hydride filled to two-thirds (1.75L) of the 2.63L total bed volume resulted in a maximum stress less than one-third of the pipe's ASME Code allowable, for hydride absorption up to a hydrogen-to-metal ratio (H/M) of 0.86. After 15 absorption/desorption tests and hydride passivation, examination of the bed interior revealed a significant decrease in particle size and increase in hydride height. The second fill level had 0.4L of fresh hydride added to the bed's cycled hydride material, and 56 absorption/desorption tests, up to a gas loading of 0.83 H/M performed. Second fill tests resulted in maximum stresses less than 40% of the ASME Code allowable. Post-test bed radiographs showed a further increase in the apparent hydride fill height, and internal component deformation

  12. In situ study of hydride precipitation kinetics and re-orientation in Zircaloy using synchrotron radiation

    International Nuclear Information System (INIS)

    The orientation and distribution of hydrides formed in zirconium alloy nuclear fuel cladding can strongly influence material behavior and in particular resistance to crack growth. The hydride microstructure and hydride platelet orientation (whether in-plane or radial relative to the cladding tubes) are crucial to determining cladding failure limits during mechanical testing. Hydride formation is normally studied by post-facto metallography, performed at room temperature and in the absence of applied stress. This study uses synchrotron radiation to observe in situ the kinetics of hydride dissolution and precipitation in previously hydrided Zircaloy samples. The experiments allow the direct observation of hydride dissolution, re-precipitation, and re-orientation, during heating and cooling under load. The solubility limits and the hydride-matrix orientation relationship determined from in situ experiments were in good agreement with previous post-facto examinations of bulk materials. The present measurements performed under stress and at temperature showed a characteristic diffraction signature of reoriented hydrides. The results suggest a threshold stress for hydride re-orientation between 75 and 80 MPa for the microstructure/texture studied. These results are discussed in light of existing knowledge.

  13. Composite Materials for Hazard Mitigation of Reactive Metal Hydrides.

    Energy Technology Data Exchange (ETDEWEB)

    Pratt, Joseph William; Cordaro, Joseph Gabriel; Sartor, George B.; Dedrick, Daniel E.; Reeder, Craig L.

    2012-02-01

    In an attempt to mitigate the hazards associated with storing large quantities of reactive metal hydrides, polymer composite materials were synthesized and tested under simulated usage and accident conditions. The composites were made by polymerizing vinyl monomers using free-radical polymerization chemistry, in the presence of the metal hydride. Composites with vinyl-containing siloxane oligomers were also polymerized with and without added styrene and divinyl benzene. Hydrogen capacity measurements revealed that addition of the polymer to the metal hydride reduced the inherent hydrogen storage capacity of the material. The composites were found to be initially effective at reducing the amount of heat released during oxidation. However, upon cycling the composites, the mitigating behavior was lost. While the polymer composites we investigated have mitigating potential and are physically robust, they undergo a chemical change upon cycling that makes them subsequently ineffective at mitigating heat release upon oxidation of the metal hydride. Acknowledgements The authors would like to thank the following people who participated in this project: Ned Stetson (U.S. Department of Energy) for sponsorship and support of the project. Ken Stewart (Sandia) for building the flow-through calorimeter and cycling test stations. Isidro Ruvalcaba, Jr. (Sandia) for qualitative experiments on the interaction of sodium alanate with water. Terry Johnson (Sandia) for sharing his expertise and knowledge of metal hydrides, and sodium alanate in particular. Marcina Moreno (Sandia) for programmatic assistance. John Khalil (United Technologies Research Corp) for insight into the hazards of reactive metal hydrides and real-world accident scenario experiments. Summary In an attempt to mitigate and/or manage hazards associated with storing bulk quantities of reactive metal hydrides, polymer composite materials (a mixture of a mitigating polymer and a metal hydride) were synthesized and tested

  14. Effect of alloy elements and hydride morphology on hydrogen embrittlement of zirconium alloy

    International Nuclear Information System (INIS)

    The effects of Nb and Sn on hydride embrittlement of Zr alloys were investigated. For this, experimental Zr alloys were prepared in a sheet shape and charged with hydrogen. The microstructure and hydride morphology were analyzed and the tensile properties were measured to understand the role of Nb and Sn on the hydride embrittlement of Zr alloy. With addition of Nb and Sn, recrystallization was retarded during the final annealing heat treatment. The retardation was mainly caused from β-Nb precipitates and Sn solute atoms, which was confirmed from texture analyses. Of the two, Sn was found to more effective in retarding recrystallization. When hydrogen was charged, hydride clusters with stacked hydride platelets were observed in unalloyed Zr. However, with addition of Nb and Sn, such hydride clusters were replaced with hydrides platelets which were more or less aligned with the rolling direction and linked up on the rolling plane, and hydride length and the spacing between hydrides were increased. This change in hydride morphology was caused by the retardation of recrystallization. Again, Sn was found to be more effective in in modifying the hydride morphology and aligning hydrides on the rolling plane. Both Nb and Sn contributed to the strengthening of Zr alloys, but Sn is more effective in strengthening than Nb. However, tensile strengths of the experimental alloys were nearly independent of the absorbed hydrogen contents. While ductility was reduced with increasing hydrogen contents, the degree of ductility loss was dependent on Nb and Sn contents which increased hydrogen solubility and retarded recrystallization. For alloys with 1%-Nb and/or 1%-Sn, increase in hydrogen solubility was the main contributor to increase in resistance to hydride embrittlement. On the other hand, for an alloy with 2%-Nb resulted in large amount of β-Nb precipitates, which in turn significantly retarded recrystallization. Therefore, the added contribution of retardation of

  15. Process optimization and kinetics for leaching of rare earth metals from the spent Ni-metal hydride batteries.

    Science.gov (United States)

    Meshram, Pratima; Pandey, B D; Mankhand, T R

    2016-05-01

    Nickel-metal hydride batteries (Ni-MH) contain not only the base metals, but valuable rare earth metals (REMs) viz. La, Sm, Nd, Pr and Ce as well. In view of the importance of resource recycling and assured supply of the contained metals in such wastes, the present study has focussed on the leaching of the rare earth metals from the spent Ni-MH batteries. The conditions for the leaching of REMs from the spent batteries were optimized as: 2M H2SO4, 348K temperature and 120min of time at a pulp density (PD) of 100g/L. Under this condition, the leaching of 98.1% Nd, 98.4% Sm, 95.5% Pr and 89.4% Ce was achieved. Besides the rare earth metals, more than 90% of base metals (Ni, Co, Mn and Zn) were also leached out in this condition. Kinetic data for the dissolution of all the rare earth metals showed the best fit to the chemical control shrinking core model. The leaching of metals followed the mechanism involving the chemical reaction proceeding on the surface of particles by the lixiviant, which was corroborated by the XRD phase analysis and SEM-EDS studies. The activation energy of 7.6, 6.3, 11.3 and 13.5kJ/mol was acquired for the leaching of neodymium, samarium, praseodymium and cerium, respectively in the temperature range 305-348K. From the leach liquor, the mixed rare earth metals were precipitated at pH∼1.8 and the precipitated REMs was analyzed by XRD and SEM studies to determine the phases and the morphological features. PMID:26746588

  16. FEASIBILITY OF RECYCLING PLUTONIUM AND MINOR ACTINIDES IN LIGHT WATER REACTORS USING HYDRIDE FUEL

    International Nuclear Information System (INIS)

    The objective of this DOE NERI program sponsored project was to assess the feasibility of improving the plutonium (Pu) and minor actinide (MA) recycling capabilities of pressurized water reactors (PWRs) by using hydride instead of oxide fuels. There are four general parts to this assessment: (1) Identifying promising hydride fuel assembly designs for recycling Pu and MAs in PWRs; (2) Performing a comprehensive systems analysis that compares the fuel cycle characteristics of Pu and MA recycling in PWRs using the promising hydride fuel assembly designs identified in Part 1 versus using oxide fuel assembly designs; (3) Conducting a safety analysis to assess the likelihood of licensing hydride fuel assembly designs; and (4) Assessing the compatibility of hydride fuel with cladding materials and water under typical PWR operating conditions Hydride fuel was found to offer promising transmutation characteristics and is recommended for further examination as a possible preferred option for recycling plutonium in PWRs

  17. FEASIBILITY OF RECYCLING PLUTONIUM AND MINOR ACTINIDES IN LIGHT WATER REACTORS USING HYDRIDE FUEL

    Energy Technology Data Exchange (ETDEWEB)

    Greenspan, Ehud; Todreas, Neil; Taiwo, Temitope

    2009-03-10

    The objective of this DOE NERI program sponsored project was to assess the feasibility of improving the plutonium (Pu) and minor actinide (MA) recycling capabilities of pressurized water reactors (PWRs) by using hydride instead of oxide fuels. There are four general parts to this assessment: 1) Identifying promising hydride fuel assembly designs for recycling Pu and MAs in PWRs 2) Performing a comprehensive systems analysis that compares the fuel cycle characteristics of Pu and MA recycling in PWRs using the promising hydride fuel assembly designs identified in Part 1 versus using oxide fuel assembly designs 3) Conducting a safety analysis to assess the likelihood of licensing hydride fuel assembly designs 4) Assessing the compatibility of hydride fuel with cladding materials and water under typical PWR operating conditions Hydride fuel was found to offer promising transmutation characteristics and is recommended for further examination as a possible preferred option for recycling plutonium in PWRs.

  18. Formation and growth of hydride blisters in Zr-2.5Nb pressure tubes

    International Nuclear Information System (INIS)

    Hydride blisters were formed on the outer surface of Zr-2.5Nb pressure tube by a nonuniform steady thermal diffusion process. A thermal gradient was applied to the pressure tube with a heat bath kept at a temperature of 415 .deg. C and an aluminum cold finger cooled with flowing water of 15 .deg. C. Optical microscopy and three-dimensional laser profilometry were used to characterize the hydride blisters with different hydrogen concentrations and thermal diffusion time. Hydride blisters were expected to start at a hydrogen concentration of 30 - 70 ppm and a thermal diffusion time of 4 - 6x105 sec. The hydride blister size increases with higher hydrogen concentrations and longer thermal diffusion time. Some of the samples revealed cracks on the hydride blisters. The ratio of hydride blister depth to height was estimated as approximately 8:1

  19. Molecular early main group metal hydrides: synthetic challenge, structures and applications.

    Science.gov (United States)

    Harder, Sjoerd

    2012-11-25

    Within the general area of early main group metal chemistry, the controlled synthesis of well-defined metal hydride complexes is a rapidly developing research field. As group 1 and 2 metal complexes are generally highly dynamic and lattice energies for their [MH](∞) and [MH(2)](∞) salts are high, the synthesis of well-defined soluble hydride complexes is an obvious challenge. Access to molecular early main group metal hydrides, however, is rewarding: these hydrocarbon-soluble metal hydrides are highly reactive, have found use in early main group metal catalysis and are potentially also valuable molecular model systems for polar metal hydrides as a hydrogen storage material. The article focusses specifically on alkali and alkaline-earth metal hydride complexes and discusses the synthetic challenge, molecular structures, reactivity and applications. PMID:23012695

  20. On the high-pressure superconducting phase in platinum hydride

    Science.gov (United States)

    Szczȩśniak, D.; Zemła, T. P.

    2015-08-01

    Motivated by the ambiguous experimental data for the superconducting phase in silane (SiH4), which may originate from platinum hydride (PtH), we provide a theoretical study of the superconducting state in the latter alloy. The quantitative estimates of the thermodynamics of PtH at 100 GPa are given for a wide range of Coulomb pseudopotential values ({μ }*) within the Eliashberg formalism. The obtained critical temperature value ({T}{{C}}\\in for {μ }*\\in ) agrees well with the experimental TC for SiH4, which may be ascribed to PtH. Moreover, the calculated characteristic thermodynamic ratios exceed the predictions of the Bardeen-Cooper-Schrieffer theory, implying the occurrence of strong-coupling and retardation effects in PtH. We note that our results may be of high relevance for future theoretical and experimental studies on hydrides.

  1. X-ray photoemission spectroscopy study of zirconium hydride

    International Nuclear Information System (INIS)

    X-ray photoemission spectroscopy (XPS) measurements are reported for ZrH/sub 1.65/ and Zr metal. The valence-band measurements are compared with available band-theory density-of-states calculations for the metal and hydride. The hydride spectrum differs significantly from the metal spectrum. Most important, a strong peak associated with hydrogen s electrons appears approximately 7 eV below the Fermi level. XPS measurements of Zr 4p core levels show a binding-energy shift of 1 eV between Zr metal and ZrH/sub 1.65/. It is argued that this shift results from charge readjustment in the vicinity of the Zr site. With the addition of hydrogen, net charge must be transferred from the Zr site to the hydrogen site. A charge-density analysis based on simplified cluster calculations is presented

  2. Effects of metastability on hydrogen sorption in fluorine substituted hydrides

    Energy Technology Data Exchange (ETDEWEB)

    Pinatel, E.R.; Corno, M.; Ugliengo, P.; Baricco, M., E-mail: marcello.baricco@unito.it

    2014-12-05

    Highlights: • Fluorine substitution in simple metal hydrides has been modelled. • The stability of the MH{sub (1−x)}F{sub x} solid solutions has been discussed. • Conditions for reversibility of sorption reactions have been suggested. - Abstract: In this work ab initio calculations and Calphad modelling have been coupled to describe the effect of fluorine substitution on the thermodynamics of hydrogenation–dehydrogenation in simple hydrides (NaH, AlH{sub 3} and CaH{sub 2}). These example systems have been used to discuss the conditions required for the formation of a stable hydride–fluoride solid solution necessary to obtain a reversible hydrogenation reaction.

  3. Hydride precipitation in zirconium studied by pendulum techniques

    International Nuclear Information System (INIS)

    Measurements of the precipitation peak, the autotwisting strain and the properties of hydride dislocations have been used to map the hydrogen terminal solid solubility boundary in polycrystalline samples and a single-crystal sample of α-zirconium. A low-frequency torsion pendulum was employed for some of the measurements and a low-frequency flexure pendulum for others. These pendulum techniques were successful in extending measurements of the hydrogen terminal solid solubility boundary in α-zirconium to the relatively low hydrogen concentration range 2 to 50 μg/g of technological interest in the nuclear industry. In addition, the results were used to obtain qualitative and quantitative information about the stress dependence of the hydrogen terminal solid solubility boundary and the kinetics of hydride precipitation or dissolution in response to a step change in the applied stress

  4. Detecting low concentrations of plutonium hydride with magnetization measurements

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Jae Wook; Mun, E. D.; Baiardo, J. P.; Zapf, V. S.; Mielke, C. H. [National High Magnetic Field Laboratory, MPA-CMMS, Los Alamos National Laboratory (LANL), Los Alamos, New Mexico 87545 (United States); Smith, A. I.; Richmond, S.; Mitchell, J.; Schwartz, D. [Nuclear Material Science Group, MST-16, LANL, Los Alamos, New Mexico 87545 (United States)

    2015-02-07

    We report the formation of plutonium hydride in 2 at. % Ga-stabilized δ-Pu, with 1 at. % H charging. We show that magnetization measurements are a sensitive, quantitative measure of ferromagnetic plutonium hydride against the nonmagnetic background of plutonium. It was previously shown that at low hydrogen concentrations, hydrogen forms super-abundant vacancy complexes with plutonium, resulting in a bulk lattice contraction. Here, we use magnetization, X-ray, and neutron diffraction measurements to show that in addition to forming vacancy complexes, at least 30% of the H atoms bond with Pu to precipitate PuH{sub x} on the surface of the sample with x ∼ 1.9. We observe magnetic hysteresis loops below 40 K with magnetic remanence, consistent with ferromagnetic PuH{sub 1.9}.

  5. Detecting low concentrations of plutonium hydride with magnetization measurements

    International Nuclear Information System (INIS)

    We report the formation of plutonium hydride in 2 at. % Ga-stabilized δ-Pu, with 1 at. % H charging. We show that magnetization measurements are a sensitive, quantitative measure of ferromagnetic plutonium hydride against the nonmagnetic background of plutonium. It was previously shown that at low hydrogen concentrations, hydrogen forms super-abundant vacancy complexes with plutonium, resulting in a bulk lattice contraction. Here, we use magnetization, X-ray, and neutron diffraction measurements to show that in addition to forming vacancy complexes, at least 30% of the H atoms bond with Pu to precipitate PuHx on the surface of the sample with x ∼ 1.9. We observe magnetic hysteresis loops below 40 K with magnetic remanence, consistent with ferromagnetic PuH1.9

  6. Development of a novel metal hydride-air secondary battery

    Energy Technology Data Exchange (ETDEWEB)

    Gamburzev, S.; Zhang, W.; Velev, O.A.; Srinivasan, S.; Appleby, A.J. [Texas A and M University, College Station (United States). Center for Electrochemical Systems and Hydrogen Research; Visintin, A. [Universidad Nacional de La Plata (Argentina). Insituto Nacional de Investigaciones Fisicoquimica Teoricas y Applicadas

    1998-05-01

    A laboratory metal hydride/air cell was evaluated. Charging was via a bifunctional air gas-diffusion electrode. Mixed nickel and cobalt oxides, supported on carbon black and activated carbon, were used as catalysts in this electrode. At 30 mA cm{sup -2} in 6 M KOH, the air electrode potentials were -0.2 V (oxygen reduction) and +0.65 V (oxygen evolution) vs Hg/HgO. The laboratory cell was cycled for 50 cycles at the C/2 rate (10 mA cm{sup -2}). The average discharge/charge voltages of the cell were 0.65 and 1.6 V, respectively. The initial capacity of the metal hydride electrode decreased by about 15% after 50 cycles. (author)

  7. Influence of oxide layer on hydrogen desorption from zirconium hydride

    International Nuclear Information System (INIS)

    Hydrogen desorption from zirconium hydride with hydrogen content of 1.95 H/Zr in He and He-5%O2 atmospheres was studied by thermal desorption spectroscopy (TDS). The morphology, structure and valence states of the oxide layer formed on the surface of zirconium hydride were analyzed by scanning electron microscopy (SEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). It was found that hydrogen desorption is retarded in the presence of oxygen. Heating in He leads to a large desorption range starting at 500 deg. C while heating in He-5%O2 atmosphere delays decomposition to relatively higher temperature of 525 deg. C. A protective oxide layer composed of monoclinic ZrO2 and small amount of tetragonal ZrO1.88, which acts as a very effective diffusion barrier. The O-H bond was observed in the oxide layer, which is beneficial to fix hydrogen atoms and prevent hydrogen diffusion

  8. Effect of thermo-mechanical cycling on zirconium hydride reorientation studied in situ with synchrotron X-ray diffraction

    Science.gov (United States)

    Colas, Kimberly B.; Motta, Arthur T.; Daymond, Mark R.; Almer, Jonathan D.

    2013-09-01

    The circumferential hydrides normally present in nuclear reactor fuel cladding after reactor exposure may dissolve during drying for dry storage and re-precipitate when cooled under load into a more radial orientation, which could embrittle the fuel cladding. It is necessary to study the rates and conditions under which hydride reorientation may happen in order to assess fuel integrity in dry storage. The objective of this work is to study the effect of applied stress and thermal cycling on the hydride morphology in cold-worked stress-relieved Zircaloy-4 by combining conventional metallography and in situ X-ray diffraction techniques. Metallography is used to study the evolution of hydride morphology after several thermo-mechanical cycles. In situ X-ray diffraction performed at the Advanced Photon Source synchrotron provides real-time information on the process of hydride dissolution and precipitation under stress during several thermal cycles. The detailed study of diffracted intensity, peak position and full-width at half-maximum provides information on precipitation kinetics, elastic strains and other characteristics of the hydride precipitation process. The results show that thermo-mechanical cycling significantly increases the radial hydride fraction as well as the hydride length and connectivity. The radial hydrides are observed to precipitate at a lower temperature than circumferential hydrides. Variations in the magnitude and range of hydride strains due to reorientation and cycling have also been observed. These results are discussed in light of existing models and experiments on hydride reorientation. The study of hydride elastic strains during precipitation shows marked differences between circumferential and radial hydrides, which can be used to investigate the reorientation process. Cycling under stress above the threshold stress for reorientation drastically increases both the reoriented hydride fraction and the hydride size. The reoriented hydride

  9. Thermal expansion and stability of cerium-doped Lu2SiO5

    International Nuclear Information System (INIS)

    In-situ X-ray diffraction, differential scanning calorimetry and dilatometry were used to measure the thermal expansion and thermal stability of cerium-doped Lu2SiO5. The thermal expansion of Lu2SiO5 was highly anisotropic, with expansion along the b- and c-axes 5-10 times greater than expansion along the a-axis. There were no measurable differences in the thermal expansion between undoped Lu2SiO5, cerium-doped Lu2SiO5 with high scintillation efficiency, cerium-doped Lu2SiO5 with low scintillation efficiency and annealed cerium-doped Lu2SiO5. Lu2SiO5 decomposed at temperatures as low as 1350 deg. C in 2, while the presence of 100-150 ppm O2 stabilized Lu2SiO5 at temperatures up to 1760 deg. C. No bulk defects were identified to account for the difference between high scintillation efficiency and low scintillation efficiency cerium-doped Lu2SiO5 samples

  10. Electrochemical deposition of cerium on porous silicon to improve photoluminescence properties

    International Nuclear Information System (INIS)

    In this work, we present results for Cerium (Ce) doping effects on photoluminescence (PL) properties of porous silicon (PS). Cerium was deposited using electrochemical deposition on porous silicon prepared by electrochemical anodization of P-type (100) Si. From the photoluminescence spectroscopy, it was shown that porous silicon treated with cerium can lead to an increase of photoluminescence when they are irradiated by light compared to the porous silicon layer without cerium. In order to understand the contribution of cerium to the enhanced photoluminescence, energy dispersive X-ray (EDX) spectroscopy, Fourier transmission infrared spectroscopy (FTIR), X-ray diffraction (XRD) and atomic force microscopy (AFM) were performed, and it was shown that the improved photoluminescence may be attributed to the change of Si–H bonds into Si–O–Ce bonds and to a newly formed PS layer during electrochemical Ce coating. - Highlights: ► Degradation of the surface structures and the PL properties of PS remains a key issue for industrial production. ► In order to solve this problem, the passivation of the PS surface by treating it with Ce is investigated. ► To understand the effects of Ce on PL properties, EDX, FTIR, XRD, AFM and UV–vis analysis were performed.

  11. Electrochemical deposition of cerium on porous silicon to improve photoluminescence properties

    Energy Technology Data Exchange (ETDEWEB)

    Atyaoui, Malek, E-mail: atyaoui.malek@yahoo.fr [Laboratoire de Photovoltaieque, Centre de Recherches et des Technologies de l' energie, PB:95, Hammam Lif 2050 (Tunisia); Dimassi, Wissem; Monther, Ghrib; Chtourou, Radhouane; Ezzaouia, Hatem [Laboratoire de Photovoltaieque, Centre de Recherches et des Technologies de l' energie, PB:95, Hammam Lif 2050 (Tunisia)

    2012-02-15

    In this work, we present results for Cerium (Ce) doping effects on photoluminescence (PL) properties of porous silicon (PS). Cerium was deposited using electrochemical deposition on porous silicon prepared by electrochemical anodization of P-type (100) Si. From the photoluminescence spectroscopy, it was shown that porous silicon treated with cerium can lead to an increase of photoluminescence when they are irradiated by light compared to the porous silicon layer without cerium. In order to understand the contribution of cerium to the enhanced photoluminescence, energy dispersive X-ray (EDX) spectroscopy, Fourier transmission infrared spectroscopy (FTIR), X-ray diffraction (XRD) and atomic force microscopy (AFM) were performed, and it was shown that the improved photoluminescence may be attributed to the change of Si-H bonds into Si-O-Ce bonds and to a newly formed PS layer during electrochemical Ce coating. - Highlights: Black-Right-Pointing-Pointer Degradation of the surface structures and the PL properties of PS remains a key issue for industrial production. Black-Right-Pointing-Pointer In order to solve this problem, the passivation of the PS surface by treating it with Ce is investigated. Black-Right-Pointing-Pointer To understand the effects of Ce on PL properties, EDX, FTIR, XRD, AFM and UV-vis analysis were performed.

  12. Catalysts with Cerium in a Membrane Reactor for the Removal of Formaldehyde Pollutant from Water Effluents

    Directory of Open Access Journals (Sweden)

    Mirella Gutiérrez-Arzaluz

    2016-05-01

    Full Text Available We report the synthesis of cerium oxide, cobalt oxide, mixed cerium, and cobalt oxides and a Ce–Co/Al2O3 membrane, which are employed as catalysts for the catalytic wet oxidation (CWO reaction process and the removal of formaldehyde from industrial effluents. Formaldehyde is present in numerous waste streams from the chemical industry in a concentration low enough to make its recovery not economically justified but high enough to create an environmental hazard. Common biological degradation methods do not work for formaldehyde, a highly toxic but refractory, low biodegradability substance. The CWO reaction is a recent, promising alternative that also permits much lower temperature and pressure conditions than other oxidation processes, resulting in economic benefits. The CWO reaction employing Ce- and Co-containing catalysts was carried out inside a slurry batch reactor and a membrane reactor. Experimental results are reported. Next, a mixed Ce–Co oxide film was supported on an γ-alumina membrane used in a catalytic membrane reactor to compare formaldehyde removal between both types of systems. Catalytic materials with cerium and with a relatively large amount of cerium favored the transformation of formaldehyde. Cerium was present as cerianite in the catalytic materials, as indicated by X-ray diffraction patterns.

  13. Catalysts with Cerium in a Membrane Reactor for the Removal of Formaldehyde Pollutant from Water Effluents.

    Science.gov (United States)

    Gutiérrez-Arzaluz, Mirella; Noreña-Franco, Luis; Ángel-Cuevas, Saúl; Mugica-Álvarez, Violeta; Torres-Rodríguez, Miguel

    2016-01-01

    We report the synthesis of cerium oxide, cobalt oxide, mixed cerium, and cobalt oxides and a Ce-Co/Al₂O₃ membrane, which are employed as catalysts for the catalytic wet oxidation (CWO) reaction process and the removal of formaldehyde from industrial effluents. Formaldehyde is present in numerous waste streams from the chemical industry in a concentration low enough to make its recovery not economically justified but high enough to create an environmental hazard. Common biological degradation methods do not work for formaldehyde, a highly toxic but refractory, low biodegradability substance. The CWO reaction is a recent, promising alternative that also permits much lower temperature and pressure conditions than other oxidation processes, resulting in economic benefits. The CWO reaction employing Ce- and Co-containing catalysts was carried out inside a slurry batch reactor and a membrane reactor. Experimental results are reported. Next, a mixed Ce-Co oxide film was supported on an γ-alumina membrane used in a catalytic membrane reactor to compare formaldehyde removal between both types of systems. Catalytic materials with cerium and with a relatively large amount of cerium favored the transformation of formaldehyde. Cerium was present as cerianite in the catalytic materials, as indicated by X-ray diffraction patterns. PMID:27231888

  14. The kinetics of bromate-cerium(III) and -iron(II) reactions

    International Nuclear Information System (INIS)

    The bromate-cerium(III) and -iron(II) reactions in acidic media were examined with special reference to their induction periods and reaction rates. In the bromate-cerium(III)reaction, the induction period is followed by a burst of cerium (IV) formation and then a gradual formation of cerium(IV). In the bromate-iron(II) reaction, a slow decrease occurs only in acidic media, even without bromate, so it may differ from the decrease in the tris(1, 10-phenanthroline)iron(II) concentration based on the oxidation by bromate. Itwas interpreted as the dissociation from ( Fe(phen)3 ) 2+ to ( Fe(phen)2 ) 2+ and phen. This is the induction period for iron(III) formation, which follows as the burst. The induction period and the rates of cerium(IV) or iron(III) formation can be interpreted on the basis of the mechanism for the Belousov oscillatory and the present redox reactions proposed by Noyes and his co-workers. (author)

  15. Effect of cerium loading on structure and morphology of modified Ce-USY zeolites

    Energy Technology Data Exchange (ETDEWEB)

    Garcia, Fillipe A.C.; Araujo, Daniel R.; Silva, Junia C.M.; Macedo, Julio L. de; Dias, Silvia C.L.; Dias, Jose A., E-mail: scdias@unb.br, E-mail: jdias@unb.br [Laboratorio de Catalise, Instituto de Quimica, Faculdade UnB-Gama, Universidade de Brasilia, DF (Brazil); Ghesti, Grace F. [Engenharia de Energia, Faculdade UnB-Gama, Universidade de Brasilia, DF (Brazil); Filho, Geraldo N.R. [Centro de Ciencias Exatas e Naturais, Universidade Federal do Para, Belem, PA (Brazil)

    2011-09-15

    This work describes comprehensibly the effect of cerium loading on the structure and morphology of NH{sub 4}USY zeolite. The Ce-USY (2-25 wt.% of CeO{sub 2}) was obtained by wet impregnation of CeCl{sub 3} followed by calcination at 550 deg C for 8 h. At low loadings (2-10%), cerium species are mainly located at ion exchange positions in the framework, whereas at higher loadings (15.25%), small aggregates were formed on the HUSY surface. X-ray diffractograms (XRD) exhibited only the reflections related to HUSY, demonstrating the high dispersion of cerium species, but Fourier transform Raman spectroscopy (FT-Raman) detected CeO{sub x} for the materials above 10%. Reaction of CeCl{sub 3} with NH{sub 4}USY produced NH{sub 4}Cl, which decomposed to form HCl, leading to framework dealumination. The materials showed an increased Lewis/Bronsted ratio with increasing cerium loadings due to the interaction between the excess cerium and the OH groups of USY, and the consequent formation of CeO{sub x} species. (author)

  16. In-house SAD phasing with surface-bound cerium ions

    International Nuclear Information System (INIS)

    Cerium was used to enhance the anomalous signal in hen egg-white lysozyme crystals and led to successful in-house SAD phasing. The anomalous signal of cerium(III) ions present in a derivative of hen egg-white lysozyme (HEWL) crystals obtained by the addition of 0.025 M cerium chloride to the crystallization medium was used for phasing. X-ray intensity data were collected to 2 Å resolution using an in-house Cu Kα radiation data-collection facility. Phasing of a single-wavelength data set purely based on its f′′ led to a clearly interpretable electron-density map. Automated substructure solution by AutoSol in PHENIX resulted in four highest peaks corresponding to cerium(III) ions with data limited to 3 Å resolution, and about 90% of the residues were built automatically by AutoBuild in PHENIX. Cerium(III) ions bound on the surface of the enzyme are found to interact mainly with the main-chain and side-chain carbonyl groups of Asn, Glu, Tyr and Asp and with water molecules. Ce3+ ions were used as potential anomalous scatterers for the in-house single-wavelength anomalous scattering technique, and this is proposed as a tool for macromolecular phasing and for the study of the interactions of trivalent metal ions with proteins and other macromolecules

  17. Synthesis and catalytic properties of microemulsion-derived cerium oxide nanoparticles

    Science.gov (United States)

    Kockrick, Emanuel; Schrage, Christian; Grigas, Anett; Geiger, Dorin; Kaskel, Stefan

    2008-07-01

    The synthesis of cerium dioxide nanoparticles using an inverse microemulsion technique and precipitation method was investigated. Cerium hydroxide nanoparticles were synthesized by adding diluted ammonia to n-heptane-surfactant-cerium nitrate system. The micelle and particle size in the range of 5-12 nm were controlled by varying the molar water to surfactant ratio and analyzed by dynamic light scattering (DLS), small angle X-ray scattering (SAXS) and high-resolution transmission electron microscopy (HRTEM). Cerium hydroxide nanoparticles were isolated and subsequently treated at 100-600 °C to obtain nanoscale ceria. Crystallite sizes of cerium dioxide in the range of 6-16 nm were estimated by Scherrer analysis by X-ray diffraction (XRD) and HRTEM. The catalytic activity of particles annealed at 400 and 600 °C in soot combustion reactions was characterized by temperature-programmed oxidation (TPO) indicating a size-dependant activity. Crystallite sizes and catalytic stability of elevated ceria systems were tested in second combustion cycles.

  18. Ground-state energy and relativistic corrections for positronium hydride

    International Nuclear Information System (INIS)

    Variational calculations of the ground state of positronium hydride (HPs) are reported, including various expectation values, electron-positron annihilation rates, and leading relativistic corrections to the total and dissociation energies. The calculations have been performed using a basis set of 4000 thoroughly optimized explicitly correlated Gaussian basis functions. The relative accuracy of the variational energy upper bound is estimated to be of the order of 2x10-10, which is a significant improvement over previous nonrelativistic results.

  19. Geoneutrinos and Hydridic Earth (or primordially Hydrogen-Rich Planet)

    OpenAIRE

    Bezrukov, L.; Sinev, V.

    2014-01-01

    Geoneutrino is a new channel of information about geochemical composition of the Earth. We alnalysed here the following problem. What statistics do we need to distinguish between predictions of Bulk Silicate Earth model and Hydridic Earth model for Th/U signal ratio? We obtained the simple formula for estimation of error of Th/U signal ratio. Our calculations show that we need more than $22 kt \\cdot year$ exposition for Gran-Sasso underground laboratory and Sudbury Neutrino Observatory. We ne...

  20. Scanning electron microscope techniques for studying Zircaloy corrosion and hydriding

    International Nuclear Information System (INIS)

    A procedure has been developed for preparing scanning electron microscope (SEM) samples of irradiated or unirradiated Zircaloy, suitable for oxide layer imaging, hydride concentration and morphology determination, and X-ray microanalysis (EPMA). The area fraction of the hydride phase is determined by image analysis of backscattered electron images (BEI). Measurements performed on unirradiated laboratory-hydrided samples, as well as cladding samples from pressurized water reactor (PWR) fuel irradiated to a burnup of about 40 MWd/kg U, gave good agreement with hot extraction hydrogen analysis over a wide range of hydrogen concentrations, based on the assumption that all the hydrogen i present as the δ-phase hydride. The local hydrogen concentration can be determined quantitatively with a spatial resolution of less than 100μm. This capability was used to determine the radial hydrogen concentration profiles across the cladding wall for PWR samples with different total hydrogen contents, surface oxide thicknesses, and local heat rating. The results indicated that the hydrogen concentration profile was essentially flat (uniform) across the wall thickness for the samples with a low total hydrogen content (∼200 ppm) or a negligible radial heat flux (plenum), while the samples from fueled sections with >200 ppm or a negligible radial heat flux (plenum), while the samples from fueled sections with >200 ppm H had a steep increase in the hydrogen concentration close to the outer surface. Analysis of a longitudinal section showed peak hydrogen concentrations opposite pellet interfaces a factor of two higher than in the mid-pellet region

  1. Inelastic neutron scattering from amorphous hydride of Zr2Pd

    International Nuclear Information System (INIS)

    Time-of-flight inelastic neutron scattering data was obtained on hydrided Zr2Pd metallic glass using the Crystal Analyzer Spectrometer at the Los Alamos pulsed spallation neutron source. Energy transfers from about 40 MeV to several hundred MeV were obtained with sufficiently good statistics and signal to noise ratio to show the second harmonic as well as the fundamental hydrogen optic mode

  2. Thermomechanics of hydrogen storage in metallic hydrides: modeling and analysis

    Czech Academy of Sciences Publication Activity Database

    Roubíček, Tomáš; Tomassetti, G.

    2014-01-01

    Roč. 19, č. 7 (2014), s. 2313-2333. ISSN 1531-3492 R&D Projects: GA ČR GA201/09/0917 Institutional support: RVO:61388998 Keywords : metal-hydrid phase transformation * hydrogen diffusion * swelling Subject RIV: BA - General Mathematics Impact factor: 0.768, year: 2014 http://aimsciences.org/journals/pdfs.jsp?paperID=10195&mode=full

  3. Dendritic surface morphology of palladium hydride produced by electrolytic deposition

    International Nuclear Information System (INIS)

    Conventional and high-resolution electron microscopic studies of electrolytically-deposited palladium hydride reveal a fascinating variety of surface profile morphologies. The observations provide direct information concerning the surface structure of palladium electrodes and the mechanism of electrolytic deposition of palladium black. Both classical electrochemical mechanisms and recent 'modified diffusion-limited-aggregation' computer simulations are discussed in comparison with the experimental results. 13 refs., 9 figs

  4. The calculated rovibronic spectrum of scandium hydride, ScH

    OpenAIRE

    Lodi, Lorenzo; Yurchenko, Sergei N.; Tennyson, Jonathan

    2015-01-01

    The electronic structure of six low-lying electronic states of scandium hydride, $X\\,{}^{1}\\Sigma^+$, $a\\,{}^{3}\\Delta$, $b\\,{}^{3}\\Pi$, $A\\,{}^{1}\\Delta$ $c\\,{}^{3}\\Sigma^+$, and $B\\,{}^{1}\\Pi$, is studied using multi-reference configuration interaction as a function of bond length. Diagonal and off-diagonal dipole moment, spin-orbit coupling and electronic angular momentum curves are also computed. The results are benchmarked against experimental measurements and calculations on atomic scan...

  5. Hydrogen storage materials and metal hydride-Ni batteries

    International Nuclear Information System (INIS)

    The hydrogen storage alloy is the key active material in metal hydride-Ni (MH-Ni) batteries. A brief review of hydrogen storage negative electrode materials including misch-nickel-based alloys, Laves phase alloys, magnesium-based alloys, vanadium-based solid solutions and nanotubes is presented. Current problems that need to be solved are mentioned. In addition, recent developments of MH/Ni-batteries with high power and energy are introduced

  6. Hydride effect on the tensile properties of HANA-4 alloy

    International Nuclear Information System (INIS)

    KAERI has developed some Zr-based new alloys, called HANA alloys, for high burn-up fuel cladding material. The sample specimens of HANA cladding tube material showed good performance in corrosion and creep properties at the irradiation test in Halden test reactor up to 10GW/MtU as well as the un-irradiation tests. Zirconium alloys has been used as nuclear fuel cladding material because they have satisfactory mechanical strength and corrosion resistance. It was reported that zirconium alloys responded abnormally in mechanical behavior over a certain temperature and strain rates. For example, the embrittlement of Zircaloy-4 (Zr-1.5Sn-0.2Fe-0.1Cr) alloy can be increased over 227 ∼ 427 .deg. C due to dynamic strain aging(DSA). The change of mechanical properties of HANA-4(Zr-1.5Nb-0.4Sn-0.2Fe-0.1Cr) alloy from DSA was already studied from room temperature to 500 .deg. C when its specimens had been tested with the strain rate of 1.67x10-2/s and 8.33x10-5/s. When a zirconium alloy is used in a nuclear reactor, hydrides form in it from not only external hydrogen sources such as waterside corrosion, dissolved hydrogen in coolant, water radiolysis but also internal sources such as hydrogen content in fuel pellets and moisture absorbed by the uranium dioxide fuel pellet. Hydrogen embrittlement of zirconium alloys has been extensively studied because hydrides may act as a sudden failure at very low strain. For low and medium hydrogen content, the hydrides crack during tensile loading and accelerate the ductile fracture process. To study the effect of hydride on the mechanical properties of HANA-4 cladding tube which had been finally heat-treated at 470 .deg. C, this research was done with tensile tests as an extension of the prior study

  7. Corrosion and hydridation features of RBMK type reactor technological channels

    International Nuclear Information System (INIS)

    Generalization results, obtained in the course of monitoring the corrosion state and hydridation of RBMK-1000 and RBMK-1500 reactor technological channels (TC) are presented. It is shown, that the corrosion behaviour of TC tube metal in reactors differs notably. Comparison of data on hybridization of RBMK-100 and RBMK-1500 reactor technological tubes allows one to suppose a possibly higher tendency to hydrogen absorption in Zr - 2.5% of Nb alloy under TMT-1 and TMT-2 states

  8. Computational modelling of structure and dynamics in lightweight hydrides

    OpenAIRE

    Aeberhard, Philippe C.; David, William I. F.; Edwards, Peter P.

    2012-01-01

    Hydrogen storage in lightweight hydrides continues to attract significant interest as the lack of a safe and efficient storage of hydrogen remains the major technological barrier to the widespread use of hydrogen as a fuel. The metal borohydrides Ca(BH₄)₂ and LiBH₄ form the subject of this thesis; three aspects of considerable academic interest were investigated by density functional theory (DFT) and molecular dynamics (MD) modelling. (i) High-pressure crystal structures of Ca(BH₄)₂ were pred...

  9. Proximity breakdown of hydrides in superconducting niobium cavities

    OpenAIRE

    Romanenko, A.; Barkov, F.; Cooley, L. D.; Grassellino, A.

    2012-01-01

    Many modern and proposed future particle accelerators rely on superconducting radio frequency cavities made of bulk niobium as primary particle accelerating structures. Such cavities suffer from the anomalous field dependence of their quality factors Q0. High field degradation - so-called high field Q-slope - is yet unexplained even though an empirical cure is known. Here we propose a mechanism based on the presence of proximity-coupled niobium hydrides, which can explain this effect. Further...

  10. Powder production of U-Mo alloy, HMD process (Hydriding- Milling- Dehydriding)

    International Nuclear Information System (INIS)

    Uranium-molybdenum (U-Mo) alloys can be hydrided massively in metastable γ (gamma) phase. The brittle hydride can be milled and dehydrided to acquire the desired size distributions needed for dispersion nuclear fuels. The developments of the different steps of this process called hydriding-milling- dehydriding (HMD Process) are described. Powder production scales for industrial fabrication is easily achieved with conventional equipment, small man-power and low investment. (author)

  11. High Temperature Metal Hydrides as Heat Storage Materials for Solar and Related Applications

    OpenAIRE

    Borislav Bogdanović; Michael Felderhoff

    2009-01-01

    For the continuous production of electricity with solar heat power plants the storage of heat at a temperature level around 400 °C is essential. High temperature metal hydrides offer high heat storage capacities around this temperature. Based on Mg-compounds, these hydrides are in principle low-cost materials with excellent cycling stability. Relevant properties of these hydrides and their possible applications as heat storage materials are described.

  12. High Temperature Metal Hydrides as Heat Storage Materials for Solar and Related Applications

    Directory of Open Access Journals (Sweden)

    Borislav Bogdanović

    2009-01-01

    Full Text Available For the continuous production of electricity with solar heat power plants the storage of heat at a temperature level around 400 °C is essential. High temperature metal hydrides offer high heat storage capacities around this temperature. Based on Mg-compounds, these hydrides are in principle low-cost materials with excellent cycling stability. Relevant properties of these hydrides and their possible applications as heat storage materials are described.

  13. High temperature metal hydrides as heat storage materials for solar and related applications.

    Science.gov (United States)

    Felderhoff, Michael; Bogdanović, Borislav

    2009-01-01

    For the continuous production of electricity with solar heat power plants the storage of heat at a temperature level around 400 degrees C is essential. High temperature metal hydrides offer high heat storage capacities around this temperature. Based on Mg-compounds, these hydrides are in principle low-cost materials with excellent cycling stability. Relevant properties of these hydrides and their possible applications as heat storage materials are described. PMID:19333448

  14. Oxidation of Group 8 transition-Metal Hydrides and Ionic Hydrogenation of Ketones and Aldehydes

    Energy Technology Data Exchange (ETDEWEB)

    Smith, Kjell-Tore

    1996-08-01

    Transition-metal hydrides have received considerable attention during the last decades because of their unusual reactivity and their potential as homogeneous catalysts for hydrogenation and other reactions of organic substrates. An important class of catalytic processes where transition-metal hydrides are involved is the homogeneous hydrogenation of alkenes, alkynes, ketones, aldehydes, arenes and nitro compounds. This thesis studies the oxidation of Group 8 transition-metal hydrides and the ionic hydrogenation of ketones and aldehydes.

  15. Effect of Cerium(IV)-Surfactant Reaction in Foam Decontamination

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Han Beom; Jung, Chong-Hun; Yoon, In-Ho; Kim, Chorong; Choi, Wang-Kyu [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2015-05-15

    Using foams allows the decommissioning of complex shaped facilities. The decontamination foam comprises at least one surfactant to generate the foam and one or more chemical reactants to achieve the dissolution of the contaminants at the solid surface. In order to improve the efficiency of decontamination foam, the present study attempts to find the optimum condition of chemical reagents to the foaming solution. The corrosion rate of radioactive nuclides contaminated stainless steel metal is very important factor for the foam decontamination process. The goal of this study is to develop the decontamination process for contaminated stainless steel in medium of nitric acid. Stainless steel needs a strong oxidizing agent such as Ce(IV) ion and the effects of cerium(IV). Surfactant interaction involved in foam decontamination and finally the improvement brought by formulation science. The formulation of foams loaded with strong oxidizing reagents such as Ce(IV) is an important factor. The enhanced decontamination properties of nitric acid with Ce(IV) additive on stainless steel is well known in liquid mediums. stainless steel metal is an important aspect in the foam decontamination process.

  16. Antioxidant Cerium Oxide Nanoparticles in Biology and Medicine

    Science.gov (United States)

    Nelson, Bryant C.; Johnson, Monique E.; Walker, Marlon L.; Riley, Kathryn R.; Sims, Christopher M.

    2016-01-01

    Previously, catalytic cerium oxide nanoparticles (CNPs, nanoceria, CeO2-x NPs) have been widely utilized for chemical mechanical planarization in the semiconductor industry and for reducing harmful emissions and improving fuel combustion efficiency in the automobile industry. Researchers are now harnessing the catalytic repertoire of CNPs to develop potential new treatment modalities for both oxidative- and nitrosative-stress induced disorders and diseases. In order to reach the point where our experimental understanding of the antioxidant activity of CNPs can be translated into useful therapeutics in the clinic, it is necessary to evaluate the most current evidence that supports CNP antioxidant activity in biological systems. Accordingly, the aims of this review are three-fold: (1) To describe the putative reaction mechanisms and physicochemical surface properties that enable CNPs to both scavenge reactive oxygen species (ROS) and to act as antioxidant enzyme-like mimetics in solution; (2) To provide an overview, with commentary, regarding the most robust design and synthesis pathways for preparing CNPs with catalytic antioxidant activity; (3) To provide the reader with the most up-to-date in vitro and in vivo experimental evidence supporting the ROS-scavenging potential of CNPs in biology and medicine. PMID:27196936

  17. Deposition and investigation of lanthanum-cerium hexaboride thin films

    International Nuclear Information System (INIS)

    Thin films of lanthanum-cerium hexaboride, the promising thermoelectric material for low-temperature applications, are deposited on various substrates by the electron-beam evaporation, pulsed laser deposition and magnetron sputtering. The influence of the deposition conditions on the films X-ray characteristics, composition, microstructure and physical properties, such as the resistivity and Seebeck coefficient, is studied. The preferred (100) orientation of all films is obtained from XRD traces. In the range of 780-800 deg. C deposition temperature the highest intensity of diffractions peaks and the highest degree of the preferred orientation are observed. The temperature dependence of the resistivity and the Seebeck coefficient of films are investigated in the temperature range of 4-300 K. The features appropriate to Kondo effect in the dependences ρ(T) and S(T) are detected at temperatures below 20 K. Interplay between the value of the Seebeck coefficient, metallic parameters and Kondo scattering of investigated films is discussed. - Graphical abstract: Kondo scattering in (La,Ce)B6 films: temperature dependence of the resistivity of (La,Ce)B6 films on various substrates and the ceramics La0.99Ce0.01B6

  18. Synthesis and characterization of cerium oxide by electrochemical methods

    International Nuclear Information System (INIS)

    Ceria-based materials have been synthesized by electrochemical process. Electrodeposition is an interesting cheap method which can be performed at ambient pressure and rather low temperature (less than 100 C). Moreover, it is easy to control in situ the film thickness. Ceria coatings were obtained by an indirect electrodeposition method. A potentiostatic technique (-0.7 V/SCE) was used to first reduce a hydroxide precursor (O2 or NO3-) before leading to the formation of cerium oxide after 2h of deposition time. This work focused on the characterization of ceria films deposited onto stainless steel in view of high temperature fuel cell applications. The chosen deposition conditions lead to quite adherent, homogenous and covering films. The microstructure and the crystallinity of the ceria thin layers were characterized by SEM, TEM and XRD measurements. Electrochemical microscopy (SECM) was also used to locally study the conductive properties of ceria layers and the homogeneity of the deposited films. Finally, electrochemical characterizations such as impedance spectroscopy were performed under air atmosphere. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  19. Synthesis and characterization of cerium oxide by electrochemical methods

    Energy Technology Data Exchange (ETDEWEB)

    Lair, V.; Ringuede, A. [LECA CNRS UMR 7575-ENSCP-Paris 6, Paris (France); Vermaut, P. [Groupe Metallurgie Structurale LPCS UMR CNRS, ENSCP-Paris 6, Paris (France); Griveau, S. [Ecole Nationale Superieure de Chimie de Paris, Faculty of Pharmacy, Chemical and Genetic Pharmacology Laboratory, Paris (France)

    2008-07-01

    Ceria-based materials have been synthesized by electrochemical process. Electrodeposition is an interesting cheap method which can be performed at ambient pressure and rather low temperature (less than 100 C). Moreover, it is easy to control in situ the film thickness. Ceria coatings were obtained by an indirect electrodeposition method. A potentiostatic technique (-0.7 V/SCE) was used to first reduce a hydroxide precursor (O{sub 2} or NO{sub 3}{sup -}) before leading to the formation of cerium oxide after 2h of deposition time. This work focused on the characterization of ceria films deposited onto stainless steel in view of high temperature fuel cell applications. The chosen deposition conditions lead to quite adherent, homogenous and covering films. The microstructure and the crystallinity of the ceria thin layers were characterized by SEM, TEM and XRD measurements. Electrochemical microscopy (SECM) was also used to locally study the conductive properties of ceria layers and the homogeneity of the deposited films. Finally, electrochemical characterizations such as impedance spectroscopy were performed under air atmosphere. (copyright 2008 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  20. Electron inelastic mean free paths in cerium dioxide

    Science.gov (United States)

    Krawczyk, M.; Holdynski, M.; Lisowski, W.; Sobczak, J. W.; Jablonski, A.

    2015-06-01

    Electron transport properties in CeO2 powder samples were studied by elastic-peak electron spectroscopy (EPES). Prior to EPES measurements, the CeO2 sample surface was pre-sputtered by 0.5 keV Ar ion etching. As a result, an altered layer with thickness of 1.3 nm was created. X-ray photoelectron spectroscopy (XPS) analysis revealed two chemical states of cerium Ce4+ (68%) and Ce3+ (32%) at the surface region of CeO2 sample after such treatment. The inelastic mean free path (IMFP), characterizing electron transport, was evaluated as a function of energy within the 0.5-2 keV range. Experimental IMFPs were corrected for surface excitations and approximated by the simple function λ = kEp, where λ was the IMFP, E denoted the energy (in eV), and k = 0.207 and p = 0.6343 were the fitted parameters. The IMFPs measured here were compared with IMFPs resulting from the TPP-2M predictive equation for the measured composition of oxide surface. The measured IMFPs were found to be from 3.1% to 20.3% smaller than the IMFPs obtained from the predictive formula in the energy range of 0.5-2 keV. The EPES IMFP value at 500 eV was related to the altered layer of sputtered CeO2 samples.

  1. Catalytic properties and biomedical applications of cerium oxide nanoparticles

    KAUST Repository

    Walkey, Carl D.

    2014-11-10

    Cerium oxide nanoparticles (nanoceria) have shown promise as catalytic antioxidants in the test tube, cell culture models and animal models of disease. However given the reactivity that is well established at the surface of these nanoparticles, the biological utilization of nanoceria as a therapeutic still poses many challenges. Moreover the form that these particles take in a biological environment, such as the changes that can occur due to a protein corona, are not well established. This review aims to summarize the existing literature on biological use of nanoceria, and to raise questions about what further study is needed to apply this interesting catalytic material to biomedical applications. These questions include: 1) How does preparation, exposure dose, route and experimental model influence the reported effects of nanoceria in animal studies? 2) What are the considerations to develop nanoceria as a therapeutic agent in regards to these parameters? 3) What biological targets of reactive oxygen species (ROS) and reactive nitrogen species (RNS) are relevant to this targeting, and how do these properties also influence the safety of these nanomaterials?

  2. Antioxidant Cerium Oxide Nanoparticles in Biology and Medicine.

    Science.gov (United States)

    Nelson, Bryant C; Johnson, Monique E; Walker, Marlon L; Riley, Kathryn R; Sims, Christopher M

    2016-01-01

    Previously, catalytic cerium oxide nanoparticles (CNPs, nanoceria, CeO2-x NPs) have been widely utilized for chemical mechanical planarization in the semiconductor industry and for reducing harmful emissions and improving fuel combustion efficiency in the automobile industry. Researchers are now harnessing the catalytic repertoire of CNPs to develop potential new treatment modalities for both oxidative- and nitrosative-stress induced disorders and diseases. In order to reach the point where our experimental understanding of the antioxidant activity of CNPs can be translated into useful therapeutics in the clinic, it is necessary to evaluate the most current evidence that supports CNP antioxidant activity in biological systems. Accordingly, the aims of this review are three-fold: (1) To describe the putative reaction mechanisms and physicochemical surface properties that enable CNPs to both scavenge reactive oxygen species (ROS) and to act as antioxidant enzyme-like mimetics in solution; (2) To provide an overview, with commentary, regarding the most robust design and synthesis pathways for preparing CNPs with catalytic antioxidant activity; (3) To provide the reader with the most up-to-date in vitro and in vivo experimental evidence supporting the ROS-scavenging potential of CNPs in biology and medicine. PMID:27196936

  3. Cerium doped lanthanum halides: fast scintillators for medical imaging

    International Nuclear Information System (INIS)

    This work is dedicated to two recently discovered scintillating crystals: cerium doped lanthanum halides (LaCl3:Ce3+ and LaBr3:Ce3+).These scintillators exhibit interesting properties for gamma detection, more particularly in the field of medical imaging: a short decay time, a high light yield and an excellent energy resolution. The strong hygroscopicity of these materials requires adapting the usual experimental methods for determining physico-chemical properties. Once determined, these can be used for the development of the industrial manufacturing process of the crystals. A proper comprehension of the scintillation mechanism and of the effect of defects within the material lead to new possible ways for optimizing the scintillator performance. Therefore, different techniques are used (EPR, radioluminescence, laser excitation, thermally stimulated luminescence). Alongside Ce3+ ions, self-trapped excitons are involved in the scintillation mechanism. Their nature and their role are detailed. The knowledge of the different processes involved in the scintillation mechanism leads to the prediction of the effect of temperature and doping level on the performance of the scintillator. A mechanism is proposed to explain the thermally stimulated luminescence processes that cause slow components in the light emission and a loss of light yield. Eventually the study of afterglow reveals a charge transfer to deep traps involved in the high temperature thermally stimulated luminescence. (author)

  4. Cerium toxicity, uptake and translocation in Arabidopsis thaliana seedlings

    Institute of Scientific and Technical Information of China (English)

    WANG Xue; LIN Yousheng; LIU Dongwu; XU Hengjian; LIU Tao; ZHAO Fengyun

    2012-01-01

    Arabidopsis thaliana seedlings were cultivated in 0-500 μmol/L of extraneous cerium (Ce) for 7 d to investigate the toxicity,uptake and translocation of rare earth elements (REEs).The results showed that Ce could be largely absorbed by the roots of A.thaliana and translocated to the shoots.But the uptake rates of Ce by the roots were much higher than the translocation rates from roots to shoots.Ultrastructural analysis revealed that Ce was mainly distributed on the cell wall.At higher concentration,Ce could also enter cell,destroy the ultrastructure of cells and disturb the intrinsic balance of nutrient elements of A.thaliana.Addition of Ce (50-500 μmol/L) to the culture medium significantly inhibited the elongation of primary roots,decreased chlorophyll content,rosette diameter and fresh mass of plants.The damage increased with the increase of Ce concentration in culture medium,although primary root elongation,chlorophyll content,and rosette diameter were stimulated by relatively low concentration (0.5 μmol/L) of Ce.Thus,it is speculated that REEs may become a new type contamination if we don't well control the release of REEs into the environment.

  5. Effect of Cerium(IV)-Surfactant Reaction in Foam Decontamination

    International Nuclear Information System (INIS)

    Using foams allows the decommissioning of complex shaped facilities. The decontamination foam comprises at least one surfactant to generate the foam and one or more chemical reactants to achieve the dissolution of the contaminants at the solid surface. In order to improve the efficiency of decontamination foam, the present study attempts to find the optimum condition of chemical reagents to the foaming solution. The corrosion rate of radioactive nuclides contaminated stainless steel metal is very important factor for the foam decontamination process. The goal of this study is to develop the decontamination process for contaminated stainless steel in medium of nitric acid. Stainless steel needs a strong oxidizing agent such as Ce(IV) ion and the effects of cerium(IV). Surfactant interaction involved in foam decontamination and finally the improvement brought by formulation science. The formulation of foams loaded with strong oxidizing reagents such as Ce(IV) is an important factor. The enhanced decontamination properties of nitric acid with Ce(IV) additive on stainless steel is well known in liquid mediums. stainless steel metal is an important aspect in the foam decontamination process

  6. Toenail cerium levels and risk of a first acute myocardial infarction: The EURAMIC and heavy metals study

    NARCIS (Netherlands)

    Gomez-Aracena, J.; Riemersma, R.A.; Veer, van 't P.; Kok, F.J.

    2006-01-01

    The association between cerium status and risk of first acute myocardial infarction (AMI) was examined in a case-control study in 10 centres from Europe and Israel. Cerium in toenails was assessed by neutron activation analysis in 684 cases and 724 controls aged 70years or younger. Mean concentratio

  7. Transparent yttrium hydride thin films prepared by reactive sputtering

    International Nuclear Information System (INIS)

    Research highlights: → Thin films of transparent (semiconducting) and black (metallic) yttrium hydride. → Magnetron sputtering with an yttrium target and hydrogen as a reactive gas. → Optical transmission and reflection resemble β-YH2 (black) and γ-YH3 (transparent). → XRD shows that transparent films have an expanded fcc lattice with a = 5.35 A. → Samples are stable at ambient conditions. - Abstract: Metal hydrides have earlier been suggested for utilization in solar cells. With this as a motivation we have prepared thin films of yttrium hydride by reactive magnetron sputter deposition. The resulting films are metallic for low partial pressure of hydrogen during the deposition, and black or yellow-transparent for higher partial pressure of hydrogen. Both metallic and semiconducting transparent YHx films have been prepared directly in situ without the need of capping layers and post-deposition hydrogenation. Optically the films are similar to what is found for YHx films prepared by other techniques, but the crystal structure of the transparent films differ from the well-known YH3-η phase, as they have an fcc lattice instead of hcp.

  8. Superconductivity of novel tin hydrides (SnnHm) under pressure

    Science.gov (United States)

    Mahdi Davari Esfahani, M.; Wang, Zhenhai; Oganov, Artem R.; Dong, Huafeng; Zhu, Qiang; Wang, Shengnan; Rakitin, Maksim S.; Zhou, Xiang-Feng

    2016-03-01

    With the motivation of discovering high-temperature superconductors, evolutionary algorithm USPEX is employed to search for all stable compounds in the Sn-H system. In addition to the traditional SnH4, new hydrides SnH8, SnH12 and SnH14 are found to be thermodynamically stable at high pressure. Dynamical stability and superconductivity of tin hydrides are systematically investigated. Im2-SnH8, C2/m-SnH12 and C2/m-SnH14 exhibit higher superconducting transition temperatures of 81, 93 and 97 K compared to the traditional compound SnH4 with Tc of 52 K at 200 GPa. An interesting bent H3–group in Im2-SnH8 and novel linear H in C2/m-SnH12 are observed. All the new tin hydrides remain metallic over their predicted range of stability. The intermediate-frequency wagging and bending vibrations have more contribution to electron-phonon coupling parameter than high-frequency stretching vibrations of H2 and H3.

  9. Structural and magnetic properties of DyFe3 hydrides

    International Nuclear Information System (INIS)

    The ternary hydride phases, DyFe3H/sub x/ with x = 1.7, 2.5, and 4.2 all retain the PuNi3 rhombohedral structure of DyFe3 with a maximum volume expansion of 18% for DyFe3H/sub 4.2/. All phases show a preferential expansion parallel to the c0 axis. From bulk magnetization measurements, the Dy-Fe spin compensation temperature is found to decrease linearly from 5450K for DyFe3 to 1500K for DyFe3H/sub 4.2/ with increasing volume of the hydride phases. The 161Dy Moessbauer results for the two Dy sites in the structure indicate a slight reduction occurs in free-ion moment found for DyFe3 in all hydride phases. In addition, the 57Fe Moessbauer data show that the average Fe moment for the five inequivalent Fe sites increases with hydrogen concentration up to x = 2.5

  10. Superconductivity of novel tin hydrides (SnnHm) under pressure

    Science.gov (United States)

    Mahdi Davari Esfahani, M.; Wang, Zhenhai; Oganov, Artem R.; Dong, Huafeng; Zhu, Qiang; Wang, Shengnan; Rakitin, Maksim S.; Zhou, Xiang-Feng

    2016-01-01

    With the motivation of discovering high-temperature superconductors, evolutionary algorithm USPEX is employed to search for all stable compounds in the Sn-H system. In addition to the traditional SnH4, new hydrides SnH8, SnH12 and SnH14 are found to be thermodynamically stable at high pressure. Dynamical stability and superconductivity of tin hydrides are systematically investigated. Im2-SnH8, C2/m-SnH12 and C2/m-SnH14 exhibit higher superconducting transition temperatures of 81, 93 and 97 K compared to the traditional compound SnH4 with Tc of 52 K at 200 GPa. An interesting bent H3–group in Im2-SnH8 and novel linear H in C2/m-SnH12 are observed. All the new tin hydrides remain metallic over their predicted range of stability. The intermediate-frequency wagging and bending vibrations have more contribution to electron-phonon coupling parameter than high-frequency stretching vibrations of H2 and H3. PMID:26964636

  11. Permeation analysis of tritium through the titanium hydride storage vessel

    International Nuclear Information System (INIS)

    A preliminary design of a stainless steel vessel for the long-term storage of hydrogen isotopes has been proposed. The immobilized hydrogen as a titanium hydride could be used in a stainless steel vessel for this application. The vessel as a primary package is designed to form titanium hydride and to contain the hydrogen isotopes and helium-3 produced from the tritium decay. In order to predict against the possibility of a contamination and the deterioration of the mechanical properties, a numerical calculation was carried out for a diffusion analysis of the hydrogen isotopes and helium inside the stainless steel vessel. Numerical results showed that a negligible amount of tritium would be released by a permeation through the vessel wall of a 0.7cm thickness at normal conditions over the entire period of the storage. In the case that the vessel was heated up to a temperature of 600 C for the routine condition of an activation or exothermic hydriding, it would be of little concern regarding a tritium loss or a contamination. However, when the vessel was exposed to a fire condition with a temperature of 800 C, permeation of the hydrogen through the vessel wall resulted in a serious increase in the amount of tritium escaping, in a very short time

  12. The electronic structure of zirconium in hydrided and oxidized states

    International Nuclear Information System (INIS)

    Highlights: • XANES and XPS of zirconium in oxidized and hydrided states were studied. • The variations in the XANES spectra are explained with density functional theory. • Hydrogen preferentially bonds to specific oxygen sites in the monoclinic ZrO2. • The monoclinic ZrO2 offers the strongest barrier against hydriding attack. - Abstract: Valence band energy shifts for pure zirconium and a model zirconium alloy (Zircaloy-4) in oxidized and hydrided states have been investigated with X-ray photoelectron spectroscopy (XPS) and X-ray Absorption Near-Edge Structure (XANES) technique. With XANES, we show that O/H interactions in oxidized Zr can be detected in the near-edge region of O K. Using density functional theory (DFT) simulations, we have determined where H atoms bond in the monoclinic ZrO2 lattice. The preferred stoichiometry is ZrO2:H, but the O-H bond is weak; increasing H causes the H atoms to form H2 molecules rather than O-H bonds. These interactions cause energy shifts in the Zr 3d XPS spectra. The results illustrate the complex processes of hydrogen and oxygen interactions at the Zr surface

  13. Safety aspects of tritium storage in metal hydride form

    International Nuclear Information System (INIS)

    Air or nitrogen ingress accident scenarios into JET tritium storage containers, filled with uranium or intermetallic compound (IMC) hydrides, are discussed based on the experimentally determined kinetics of the reaction of these hydrides with air, O2 and N2. Reaction of uranium with air can occur at room temperature. For the initiation of the reactions of uranium with N2 or of some intermetallic compounds with air, elevated temperatures are required. Temperature rises of the metal hydrides due to air ingress are estimated for various cases. Modern tritium storage containers are protected against air ingress by intermediate and secondary containments which can be either evacuated or filled with inert gas. Therefore, air ingress can only occur due to double failure: failure of secondary containment and process containment at the same time. At JET, the secondary containments are filled with N2. However, even for N2, temperature increases are expected during the ingress into uranium beds (U-beds) for particular scenarios. It is shown that the JET design would not fail in this event. The calculation also shows that the smallest temperature rises during air, O2 or N2 ingress are expected for a getter bed design with free space above the metal getter layer for the gas to flow from inlet to outlet tube. 14 refs., 3 figs., 4 tabs

  14. Modellization of Metal Hydride Canister for Hydrogen Storage

    Directory of Open Access Journals (Sweden)

    Rocio Maceiras

    2015-06-01

    Full Text Available Hydrogen shows very interesting features for its use on-board applications as fuel cell vehicles. This paper presents the modelling of a tank with a metal hydride alloy for on-board applications, which provides good performance under ambient conditions. The metal hydride contained in the tank is Ti0.98Zr0.02V0.43Fe0.09Cr0.05Mn1.5. A two-dimensional model has been performed for the refuelling process (absorption and the discharge process (desorption. For that, individual models of mass balance, energy balance, reaction kinetics and behaviour of hydrogen gas has been modelled. The model has been developed under Matlab / Simulink© environment. Finally, individual models have been integrated into a global model, and simulated under ambient conditions. With the aim to analyse the temperature influence on the state of charge and filling and emptying time, other simulations were performed at different temperatures. The obtained results allow to conclude that this alloy offers a good behaviour with the discharge process under normal ambient conditions. Keywords: Hydrogen storage; metal hydrides; fuel cell; simulation; board applications

  15. Hydrogen Storage using Metal Hydrides in a Stationary Cogeneration System

    International Nuclear Information System (INIS)

    In the frame of the development of a hydrogen production and storage unit to supply a 40 kW stationary fuel cell, a metal hydride storage tank was chosen according to its reliability and high energetic efficiency. The study of AB5 compounds led to the development of a composition adapted to the project needs. The absorption/desorption pressures of the hydride at 75 C (2 / 1.85 bar) are the most adapted to the specifications. The reversible storage capacity (0.95 %wt) has been optimized to our work conditions and chemical kinetics is fast. The design of the Combined Heat and Power CHP system requires 5 kg hydrogen storage but in a first phase, only a 0.1 kg prototype has been realised and tested. Rectangular design has been chosen to obtain good compactness with an integrated plate fin type heat exchanger designed to reach high absorption/desorption rates. In this paper, heat and mass transfer characteristics of the Metal Hydride tank (MH tank) during absorption/desorption cycles are given. (authors)

  16. Neutron diffraction studies of metal hydrides alloys for hydrogen storage

    International Nuclear Information System (INIS)

    In this paper we present results obtained from two different classes of metal hydrides. First, we will discuss the effect of ball milling on the hydrogen storage properties of magnesium hydride. High energy milling of MgD2 produces a nanocrystalline structure made of a mixture of β-MgD2 and the high temperature/high pressure phase γ-MgD2. Neutron powder diffraction showed that the ball-milled β-MgD2 and γ-MgD2 structures are distorted compared to the same phases synthesised at high-pressure and high temperature. The Mg-D bond lengths are modified in β-MgD2. In γ-MgD2 phase, only one bond length is changed. This may be the explanation for the limited amount of γ-MgD2 synthesized by energetic ball milling. The second case is the crystal structure of a new class of metal hydrides, the so called 'Laves phase related BCC solid solution'. From neutron diffraction, we found that two phases are present in the as-cast alloy TiV0.9Mn1.1. One is a BCC solid solution, the other is a C14 Laves phase. We found that in the C14 phase there is a preferential site for titanium atoms while the vanadium and manganese atoms are distributed on the other two sites. (author)

  17. Performance study of a hydrogen powered metal hydride actuator

    Science.gov (United States)

    Mainul Hossain Bhuiya, Md; Kim, Kwang J.

    2016-04-01

    A thermally driven hydrogen powered actuator integrating metal hydride hydrogen storage reactor, which is compact, noiseless, and able to generate smooth actuation, is presented in this article. To test the plausibility of a thermally driven actuator, a conventional piston type actuator was integrated with LaNi5 based hydrogen storage system. Copper encapsulation followed by compaction of particles into pellets, were adopted to improve overall thermal conductivity of the reactor. The operation of the actuator was thoroughly investigated for an array of operating temperature ranges. Temperature swing of the hydride reactor triggering smooth and noiseless actuation over several operating temperature ranges were monitored for quantification of actuator efficiency. Overall, the actuator generated smooth and consistent strokes during repeated cycles of operation. The efficiency of the actuator was found to be as high as 13.36% for operating a temperature range of 20 °C-50 °C. Stress-strain characteristics, actuation hysteresis etc were studied experimentally. Comparison of stress-strain characteristics of the proposed actuator with traditional actuators, artificial muscles and so on was made. The study suggests that design modification and use of high pressure hydride may enhance the performance and broaden the application horizon of the proposed actuator in future.

  18. Air passivation of metal hydride beds for waste disposal

    International Nuclear Information System (INIS)

    One waste acceptance criteria for hydride bed waste disposal is that the bed be non-pyrophoric. Batch-wise air ingress tests were performed which determined the amount of air consumed by a metal hydride bed. A desorbed, 4.4 kg titanium prototype hydride storage vessel (HSV) produced a 4.4 deg.C internal temperature rise upon the first air exposure cycle and a 0.1 deg.C temperature rise upon a second air exposure. A total of 346 sec air was consumed by the bed (0.08 sec per gram Ti). A desorbed, 9.66 kg LaNi4.25Al0.75 prototype storage bed experienced larger temperature rises over successive cycles of air ingress and evacuation. The cycles were performed over a period of days with the bed effectively passivated after the 12. cycle. Nine to ten STP-L of air reacted with the bed producing both oxidized metal and water. (authors)

  19. Multidimensional Chemical Modeling. III. Abundance and excitation of diatomic hydrides

    CERN Document Server

    Bruderer, Simon; Stäuber, P; Doty, Steven D

    2010-01-01

    The Herschel Space Observatory opens the sky for observations in the far infrared at high spectral and spatial resolution. A particular class of molecules will be directly observable; light diatomic hydrides and their ions (CH, OH, SH, NH, CH+, OH+, SH+, NH+). These simple constituents are important both for the chemical evolution of the region and as tracers of high-energy radiation. If outflows of a forming star erode cavities in the envelope, protostellar far UV (FUV; 6 100 K) for water ice to evaporate. If the cavity shape allows FUV radiation to penetrate this hot-core region, the abundance of FUV destroyed species (e.g. water) is decreased. In particular, diatomic hydrides and their ions CH$+, OH+ and NH+ are enhanced by many orders of magnitude in the outflow walls due to the combination of high gas temperatures and rapid photodissociation of more saturated species. The enhancement of these diatomic hydrides is sufficient for a detection using the HIFI and PACS instruments onboard Herschel. The effect...

  20. Effect of the hydrogen content and cooling velocity in the hydrides precipitation in α-zirconium

    International Nuclear Information System (INIS)

    Zirconium specimens containing 50-300 ppm hydrogen have been cooled from the hydrogen solution treatment temperature at different rates by furnace cooling, air cooling and oil quenching. Optical and electron microscopical investigations have revealed grain boundary Δ - hydrides in slowly cooled specimens. At higher cooling rates γ and Δ hydrides have been found precipitated both intergranularly and intragranularly. Grain boundary Δ hydrides have been also observed in oil quenched specimens with 300 ppm hydrogen. Quenched specimens have revealed Widmanstatten and parallel plate type hydride morphologies. (Author)

  1. Measurement and modeling of strain fields in zirconium hydrides precipitated at a stress concentration

    Science.gov (United States)

    Allen, Gregory B.; Kerr, Matthew; Daymond, Mark R.

    2012-11-01

    Hydrogen adsorption into zirconium, as a result of corrosion in aqueous environments, leads to the precipitation of a secondary brittle hydride phase. These hydrides tend to first form at stress concentrations such as fretting flaws or cracks in engineering components, potentially degrading the structural integrity of the component. One mechanism for component failure is a slow crack growth mechanism known as Delayed Hydride Cracking (DHC), where hydride fracture occurs followed by crack arrest in the ductile zirconium matrix. The current work employs both an experimental and a modeling approach to better characterize the effects and behavior of hydride precipitation at such stress concentrations. Strains around stress concentrations containing hydrides were mapped using High Energy X-ray Diffraction (HEXRD). These studies highlighted important differences in the behavior of the hydride phase and the surrounding zirconium matrix, as well as the strain associated with the precipitation of the hydride. A finite element model was also developed and compared to the X-ray strain mapping results. This model provided greater insight into details that could not be obtained directly from the experimental approaches, as well as providing a framework for future modeling to predict the effects of hydride precipitation under varied conditions.

  2. Mechanical characteristics of hydrides in titanium and titanium-palladium alloy

    International Nuclear Information System (INIS)

    With the aim of estimating of stress-strain curve and fracture strain of thin layer hydrides of pure titanium (Gr.1) and titanium-palladium alloy (Gr.17), we utilized dual indentation method and advanced indentation machine equipped with acoustic emission (AE) monitoring system. We first estimated stress-strain curves of two base metals and two hydrides utilizing the dual indentation method. Next we estimated the fracture strain of two hydrides by FEM method using the critical indentation force to cause the Mode-I crack in hydrides during indentation tests. The critical force was correctly determined by waveform analysis of AEs detected during indentation test. The fracture strain of hydride of Gr.1 was estimated as 8.1% and larger than that (4.3%) of Gr.17 hydride. Fracture strains of two hydrides appear to be due to the chemical composition of the hydrides. Gr.1 produced a TiH2 hydride, while Gr.1 did a TiH1.971. (author)

  3. Investigation of Liquid Metal Bonded Hydride Fuels for LWRs - A Review

    International Nuclear Information System (INIS)

    Hydride fuels have been proposed for power production applications in LWRs. The fuel consists of uranium-zirconium hydride pellets clad with Zircaloy tubing. The fuel-cladding gap is filled with a liquid lead-tin- bismuth alloy. Incentives for hydride fuel incorporation into LWRs are briefly reviewed followed by a detailed discussion of material properties, steady-state and transient behaviour, and irradiation effects on hydride fuels. The discussion is based on historical data from the SNAP program and General Atomics' TRIGA reactors and recent research conducted at Universities of Tokyo and California, Berkeley. (author)

  4. Some new techniques in tritium gas handling as applied to metal hydride synthesis

    International Nuclear Information System (INIS)

    A state-of-the-art tritium Hydride Synthesis System (HSS) was designed and built to replace the existing system within the Tritium Salt Facility (TSF) at the Los Alamos National Laboratory. This new hydriding system utilized unique fast-cycling 5.63 mole uranium beds (50.9 g to T2 at 100% loading) and novel gas circulating hydriding furnaces. Tritium system components discussed include fast-cycling uranium beds, circulating gas hydriding furnaces, valves, storage volumes, manifolds, gas transfer pumps, and graphic display and control consoles. Many of the tritium handling and processing techniques incorporated into this system are directly applicable to today's fusion fuel loops

  5. Some new techniques in tritium gas handling as applied to metal hydride synthesis

    International Nuclear Information System (INIS)

    A state-of-the-art tritium Hydriding Synthesis System (HSS) was designed and built to replace the existing system within the Tritium Salt Facility (TSF) at the Los Alamos National Laboratory. This new hydriding system utilizes unique fast-cycling 7.9 mole uranium beds (47.5g of T at 100% loading) and novel gas circulating hydriding furnaces. Tritium system components discussed include fast-cycling uranium beds, circulating gas hydriding furnaces, valves, storage volumes, manifolds, gas transfer pumps, and graphic display and control consoles. Many of the tritium handling and processing techniques incorporated into this system are directly applicable to today's fusion fuel loops. 12 refs., 7 figs

  6. Hydride phase equilibria in V-Ti-Ni alloy membranes

    International Nuclear Information System (INIS)

    Highlights: • V70Ti15Ni15 (at.%) comprises a vanadium solid solution plus NiTi and NiTi2. • Dissolution of Ni and Ti into vanadium solid solution increase critical temperature for BCT β-hydride formation. • Three VSS hydride phase fields were observed: BCC, BCC + BCT, BCT + BCT. • NiTi and NiTi2 phases do not stabilise the alloy against brittle failure. - Abstract: Vanadium is highly permeable to hydrogen which makes it one of the leading alternatives to Pd alloys for hydrogen-selective alloy membrane applications, but it is prone to brittle failure through excessive hydrogen absorption and transitions between the BCC α and BCT β phases. V-Ti-Ni alloys are a prospective class of alloy for hydrogen-selective membrane applications, comprising a highly-permeable vanadium solid solution and several interdendritic Ni-Ti compounds. These Ni-Ti compounds are thought to stabilise the alloy against brittle failure. This hypothesis was investigated through a systematic study of V70Ti15Ni15 by hydrogen absorption and X-ray diffraction under conditions relevant to membrane operation. Dissolved hydrogen concentration in the bulk alloy and component phases, phase identification, thermal and hydrogen-induced expansion, phase quantification and hydride phase transitions under a range of pressures and temperatures have been determined. The vanadium phase passes through three different phase fields (BCC, BCC + BCT, BCT + BCT) during cooling under H2 from 400 to 30 °C. Dissolution of Ni and Ti into the vanadium phase increases the critical temperature for β-hydride formation from <200 to >400 °C. Furthermore, the Ni-Ti phases also exhibit several phase transitions meaning their ability to stabilise the alloy is questionable. We conclude that this alloy is significantly inferior to V with respect to its stability when used as a hydrogen-selective membrane, but the hydride phase transitions suggest potential application for high-temperature hydrogen and thermal energy

  7. Reactivity patterns of transition metal hydrides and alkyls

    International Nuclear Information System (INIS)

    The complex PPN+ CpV(CO)3H- (Cp=eta5-C5H5 and PPN = (Ph3P)2) was prepared in 70% yield and its physical properties and chemical reactions investigated. PPN+ CpV(CO)3H- reacts with a wide range of organic halides. The organometallic products of these reactions are the vanadium halides PPN+[CpV(C)3X]- and in some cases the binuclear bridging hydride PPN+ [CpV(CO)3]2H-. The borohydride salt PPN+[CpV(CO)3BH4]- has also been prepared. The reaction between CpV(CO)3H- and organic halides was investigated and compared with halide reductions carried out using tri-n-butyltin hydride. Results demonstrate that in almost all cases, the reduction reaction proceeds via free radical intermediates which are generated in a chain process, and are trapped by hydrogen transfer from CpV(CO)3H-. Sodium amalgam reduction of CpRh(CO)2 or a mixture of CpRh(CO)2 and CpCo(CO)2 affords two new anions, PPN+ [Cp2Rh3(CO)4]- and PPN+[Cp2RhCo(CO)2]-. CpMo(CO)3H reacts with CpMo(CO)3R (R=CH3,C2H5, CH2C6H5) at 25 to 500C to produce aldehyde RCHO and the dimers [CpMo(CO)3]2 and [CpMo(CO)2]2. In general, CpV(CO)3H- appears to transfer a hydrogen atom to the metal radical anion formed in an electron transfer process, whereas CpMo(CO)3H transfers hydride in a 2-electron process to a vacant coordination site. The chemical consequences are that CpV(CO)3H- generally reacts with metal alkyls to give alkanes via intermediate alkyl hydride species whereas CpMo(CO)3H reacts with metal alkyls to produce aldehyde, via an intermediate acyl hydride species

  8. Oxochloroalkoxide of the Cerium (IV and Titanium (IV as oxides precursor

    Directory of Open Access Journals (Sweden)

    Machado Luiz Carlos

    2002-01-01

    Full Text Available The Cerium (IV and Titanium (IV oxides mixture (CeO2-3TiO2 was prepared by thermal treatment of the oxochloroisopropoxide of Cerium (IV and Titanium (IV. The chemical route utilizing the Cerium (III chloride alcoholic complex and Titanium (IV isopropoxide is presented. The compound Ce5Ti15Cl16O30 (iOPr4(OH-Et15 was characterized by elemental analysis, FTIR and TG/DTG. The X-ray diffraction patterns of the oxides resulting from the thermal decomposition of the precursor at 1000 degreesC for 36 h indicated the formation of cubic cerianite (a = 5.417Å and tetragonal rutile (a = 4.592Å and (c = 2.962 Å, with apparent crystallite sizes around 38 and 55nm, respectively.

  9. Mesoporous cerium oxide nanospheres for the visible-light driven photocatalytic degradation of dyes

    Directory of Open Access Journals (Sweden)

    Subas K. Muduli

    2014-04-01

    Full Text Available A facile, solvothermal synthesis of mesoporous cerium oxide nanospheres is reported for the purpose of the photocatalytic degradation of organic dyes and future applications in sustainable energy research. The earth-abundant, relatively affordable, mixed valence cerium oxide sample, which consists of predominantly Ce7O12, has been characterized by powder X-ray diffraction, X-ray photoelectron and UV–vis spectroscopy, and transmission electron microscopy. Together with N2 sorption experiments, the data confirms that the new cerium oxide material is mesoporous and absorbs visible light. The photocatalytic degradation of rhodamin B is investigated with a series of radical scavengers, suggesting that the mechanism of photocatalytic activity under visible-light irradiation involves predominantly hydroxyl radicals as the active species.

  10. Kinetics of deso/sub x/ reaction on copper and cerium-based sorbent-catalysts

    International Nuclear Information System (INIS)

    Kinetics of SO/sub 2/ removal using a copper-based sorbent CuO/gamma-AI/sub 2/O/sub 3/ and a cerium modified copper sorbent CuO-CeO/sub 2/gamma-AI/sub 2/O, were measured on a TGA and their kinetics behaviors were simulated with a proposed empirical rate model (ERM). The purpose of cerium addition to the copper sorbent was to study the difference of sorbent's kinetics. The cerium modified copper sorbent showed a higher reaction rate on initial sulfation than the regular copper sorbent. Both sorbents however had similar calculated activation energy. The proposed ERM model appeared to describe the SO/sub 2/ removal kinetics well in the temperature range 250-400 degree C. (author)

  11. Magnetic ordering in the static intermediate-valent cerium compound Ce2RuZn4

    Science.gov (United States)

    Eyert, Volker; Scheidt, Ernst-Wilhelm; Scherer, Wolfgang; Hermes, Wilfried; Pöttgen, Rainer

    2008-12-01

    The low-temperature behavior of Ce2RuZn4 has been investigated. Specific-heat and magnetic-susceptibility data reveal an antiferromagnetic transition at a Néel temperature of 2 K. Ce2RuZn4 is a static intermediate-valent compound with two crystallographically independent cerium atoms. The magnetic data clearly show that only one cerium site is magnetic (Ce3+) , while the second one carries no magnetic moment. The experimental data are interpreted with the help of first-principles electronic structure calculations using density-functional theory and the augmented spherical wave method. The calculations reveal the occurrence of two different cerium sites, which are characterized by strongly localized magnetic moments and strong Ce-Ru bonding.

  12. Electro-deposition of cerium thin film compound, elaboration and characterisation

    International Nuclear Information System (INIS)

    Cerium oxide films are widely studied as a promising alternative to the toxic hexavalent Chromium Cr(VI) based pre-treatments for the corrosion protection of different metals and alloys. Cathodic electro-deposition of Cerium compound thin films was realised on Ti alloy (TA6V) substrates from a Ce(NO3)3, 6H2O in water-ethyl alcohol solutions at 0.01 M. Experimental conditions to obtain homogeneous and crack free thin films were determined. The deposited cerium quantity, as expected, is proportional to the used electric charge, following the Faraday law. Subsequent thermal treatment led to a CeO2 coating, which is expected to increase the TA6V oxidation resistance at high temperatures. The deposits were characterized by Differential Scanning Calorimetry (DSC), optical and scanning electron microscopies.(author)

  13. Effect of Impurities and Cerium on Stress Concentration Sensitivity of Al-Li Based Alloys

    Institute of Scientific and Technical Information of China (English)

    孟亮; 田丽

    2002-01-01

    A notch sensitivity factor was derived in order to evaluate the stress concentration sensitivity of Al-Li based alloys. The factor values for the Al-Li alloy sheets containing various contents of impurities and cerium addition were evaluated by determining the mechanical properties. It is found that the impurities Fe, Si, Na and K significantly enhance the stress concentration sensitivity of the alloys 2090 and 8090, whereas cerium addition reduces the stress concentration sensitivity to a certain degree for the high strength alloys. However, an excess amount of cerium addition in the high ductility alloy 1420 can significantly increase the stress concentration sensitivity. As compared with conventional aluminum alloys, the Al-Li based alloys generally show high stress concentration sensitivity. Therefore, a special attention must be paid to this problem in the practical application of Al-Li based alloys.

  14. Self-Correction of Lanthanum-Cerium Halide Gamma Spectra (pre-print)

    Energy Technology Data Exchange (ETDEWEB)

    Ding Yuan, Paul Guss, and Sanjoy Mukhopadhyay

    2009-04-01

    Lanthanum-cerium halide detectors generally exhibit superior energy resolutions for gamma radiation detection compared with conventional sodium iodide detectors. However, they are also subject to self-activities due to lanthanum-138 decay and contamination due to beta decay in the low-energy region and alpha decay in the high-energy region. The detector’s self-activity and crystal contamination jointly contribute a significant amount of uncertainties to the gamma spectral measurement and affect the precision of the nuclide identification process. This paper demonstrates a self-correction procedure for self-activity and contamination reduction from spectra collected by lanthanum-cerium halide detectors. It can be implemented as an automatic self-correction module for the future gamma radiation detector made of lanthanum-cerium halide crystals.

  15. Self-Correction of Lanthanum-Cerium Halide Gamma Spectra (pre-print)

    International Nuclear Information System (INIS)

    Lanthanum-cerium halide detectors generally exhibit superior energy resolutions for gamma radiation detection compared with conventional sodium iodide detectors. However, they are also subject to self-activities due to lanthanum-138 decay and contamination due to beta decay in the low-energy region and alpha decay in the high-energy region. The detector's self-activity and crystal contamination jointly contribute a significant amount of uncertainties to the gamma spectral measurement and affect the precision of the nuclide identification process. This paper demonstrates a self-correction procedure for self-activity and contamination reduction from spectra collected by lanthanum-cerium halide detectors. It can be implemented as an automatic self-correction module for the future gamma radiation detector made of lanthanum-cerium halide crystals.

  16. Electrolytic technique for the chemical decontamination process with sulfuric acid-cerium (IV) for decommissioning

    International Nuclear Information System (INIS)

    An electrolyzer with an ion-exchange membrane as the separator has been used to study the electrolytic redox reaction of Ce4+ / Ce3+ in sulfuric acid solution, which is a reagent for predismantling system decontamination. Influencing factors such as current density, cerium concentration, acidity, electrolyte flow rate, membrane type and electrode material were studied experimentally. The results indicate that the redox can be achieved with high conversion even as the cerium concentration is below 0.005 M. However, the current efficiency strongly depends on the cerium concentration. In addition, the acid content and the electrolyte flow rate show little influence on the redox reaction. Both cation and anion membrane are feasible for this process. Therefore, the operation conditions are widely applicable. Moreover, two different electrode materials, platinized titanium meshes and graphite, were used. The results show that the platinized titanium meshes is preferable to the graphite for higher current efficiency. (author)

  17. Cathodic electrolysis method of depositing cerium conversion films on industrial pure aluminum

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Two two-step techniques, called TS2/TS7 and TS3/TS7, respectively, have been developed to form cerium conversion films on the surface of industrial pure aluminum. The tested material was cathodically electrolyzed in the alkaline solution containing cerium salt, and uniform films containing cerium were obtained after the two-step treatment. It is found that the films obtained by TS2/TS7 and TS3/TS7 techniques are about 4.0 and 3.0 m in thickness, respectively. The material has better corrosion resistance in the chloride solution after the two-step electrolysis treatment compared with the one-step treated and naked specimens.

  18. 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.

  19. Excitation induced spectroscopic study and quenching effect in cerium samarium codoped lithium aluminoborate glasses

    Science.gov (United States)

    Kaur, Parvinder; Kaur, Simranpreet; Singh, Gurinder Pal; Arora, Deepawali; Kumar, Sunil; Singh, D. P.

    2016-08-01

    Lithium aluminium borate host has been codoped with cerium and samarium to prepare glass by conventional melt quench technique. Their structural and spectroscopic investigation has been carried out using XRD, FTIR and density measurements. The UV-Vis absorption spectra and fluorescence spectra (λexc.=380 nm and 400 nm) have been studied for spectroscopic analysis. The amorphous nature of the prepared samples is shown by XRD. The density is increasing with addition of cerium at the expense of aluminium, keeping other components constant. FTIR study also shows the presence of compact and stable tetrahedral BO4 units thus supporting the density results. The UV- Vis absorption spectra show a shift of optical absorption edge towards longer wavelength along with an increase in intensity of peaks with rising samarium concentration. The fluorescence spectra show a blue shift and subsequent suppression of cerium peaks with addition of samarium.

  20. Catalytic spectrophotometric determination of cerium by ion exchange separation coupled to a flow injection system

    International Nuclear Information System (INIS)

    A flow injection method is described intended for the determination of cerium based on its catalytic effect on the oxidation of gallocyanine by peroxydisulfate in acidic media. The proposed flow injection manifold incorporates a ion exchange separation system in the carrier stream. The decolorisation of gallocyanine due to its oxidation was used to monitor the reaction by spectrophotometry at 524 nm. The variables which affected the reaction rate were fully investigated. By this method cerium(4) can be determined in the range of 0.30-10.0 μg with a limit of detection of 0.25 μg. The relative standard deviation for ten replicate determinations of 1.0 μg of cerium(4) was 1.8 %

  1. Protection against corrosion in marine environments of AA6060 aluminium alloy by cerium chlorides

    International Nuclear Information System (INIS)

    Lanthanide salts are being considered as an environmentally friendly alternative to the classic systems based on chromates. The addition of small concentrations of cerium chloride to aerated aqueous 3.5% NaCl solution inhibits uniform and pitting corrosion processes of AA6060. Full immersion tests combined with different electrochemical techniques were involved to determine the protection degree and the inhibition character supplied by the cerium ion. Their microscopic and compositional features have been analyzed using SEM and EDS spectra. The results obtained show that the protective layer has heterogeneous composition. An alumina layer covers the aluminium matrix while dispersed cerium-rich islands deposited over the cathodic sites of the alloy. In the case of AA6060, α-Al(Fe,Mn)Si acts as permanent cathodic sites.

  2. Exposure of cerium oxide nanoparticles to kidney bean shows disturbance in the plant defense mechanisms

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • Kidney bean roots uptake nCeO2 primarily without biotransformation. • Cerium reached the root vascular tissues through gaps in the Casparian strip. • On longer exposure to high concentration, roots demonstrate stress response. • In leaves, guaiacol peroxidase plays a major role in ROS scavenging. - Abstract: Overwhelming use of engineered nanoparticles demands rapid assessment of their environmental impacts. The transport of cerium oxide nanoparticles (nCeO2) in plants and their impact on cellular homeostasis as a function of exposure duration is not well understood. In this study, kidney bean plants were exposed to suspensions of ∼8 ± 1 nm nCeO2 (62.5 to 500 mg/L) for 15 days in hydroponic conditions. Plant parts were analyzed for cerium accumulation after one, seven, and 15 days of nCeO2 exposure. The primary indicators of stress like lipid peroxidation, antioxidant enzyme activities, total soluble protein and chlorophyll contents were studied. Cerium in tissues was localized using scanning electron microscopy and synchrotron μ-XRF mapping, and the chemical forms were identified using μ-XANES. In the root epidermis, cerium was primarily shown to exist as nCeO2, although a small fraction (12%) was biotransformed to Ce(III) compound. Cerium was found to reach the root vascular tissues and translocate to aerial parts with time. Upon prolonged exposure to 500 mg nCeO2/L, the root antioxidant enzyme activities were significantly reduced, simultaneously increasing the root soluble protein by 204%. In addition, leaf's guaiacol peroxidase activity was enhanced with nCeO2 exposure in order to maintain cellular homeostasis

  3. Exposure of cerium oxide nanoparticles to kidney bean shows disturbance in the plant defense mechanisms

    Energy Technology Data Exchange (ETDEWEB)

    Majumdar, Sanghamitra [Department of Chemistry, The University of Texas at El Paso, 500 West University Ave., El Paso, TX 79968 (United States); University of California Center for Environmental Implications of Nanotechnology (UC CEIN) (United States); Peralta-Videa, Jose R. [Department of Chemistry, The University of Texas at El Paso, 500 West University Ave., El Paso, TX 79968 (United States); Environmental Science and Engineering PhD Program, The University of Texas at El Paso, 500 West University Ave., El Paso, TX 79968 (United States); University of California Center for Environmental Implications of Nanotechnology (UC CEIN) (United States); Bandyopadhyay, Susmita [Environmental Science and Engineering PhD Program, The University of Texas at El Paso, 500 West University Ave., El Paso, TX 79968 (United States); University of California Center for Environmental Implications of Nanotechnology (UC CEIN) (United States); Castillo-Michel, Hiram [European Synchrotron Radiation Facility, B.P. 220-38043 Grenoble, Cedex (France); Hernandez-Viezcas, Jose-Angel [Department of Chemistry, The University of Texas at El Paso, 500 West University Ave., El Paso, TX 79968 (United States); University of California Center for Environmental Implications of Nanotechnology (UC CEIN) (United States); Sahi, Shivendra [Department of Biology, Western Kentucky University, Bowling Green, KY 42101 (United States); Gardea-Torresdey, Jorge L., E-mail: jgardea@utep.edu [Department of Chemistry, The University of Texas at El Paso, 500 West University Ave., El Paso, TX 79968 (United States); Environmental Science and Engineering PhD Program, The University of Texas at El Paso, 500 West University Ave., El Paso, TX 79968 (United States); University of California Center for Environmental Implications of Nanotechnology (UC CEIN) (United States)

    2014-08-15

    Graphical abstract: - Highlights: • Kidney bean roots uptake nCeO{sub 2} primarily without biotransformation. • Cerium reached the root vascular tissues through gaps in the Casparian strip. • On longer exposure to high concentration, roots demonstrate stress response. • In leaves, guaiacol peroxidase plays a major role in ROS scavenging. - Abstract: Overwhelming use of engineered nanoparticles demands rapid assessment of their environmental impacts. The transport of cerium oxide nanoparticles (nCeO{sub 2}) in plants and their impact on cellular homeostasis as a function of exposure duration is not well understood. In this study, kidney bean plants were exposed to suspensions of ∼8 ± 1 nm nCeO{sub 2} (62.5 to 500 mg/L) for 15 days in hydroponic conditions. Plant parts were analyzed for cerium accumulation after one, seven, and 15 days of nCeO{sub 2} exposure. The primary indicators of stress like lipid peroxidation, antioxidant enzyme activities, total soluble protein and chlorophyll contents were studied. Cerium in tissues was localized using scanning electron microscopy and synchrotron μ-XRF mapping, and the chemical forms were identified using μ-XANES. In the root epidermis, cerium was primarily shown to exist as nCeO{sub 2}, although a small fraction (12%) was biotransformed to Ce(III) compound. Cerium was found to reach the root vascular tissues and translocate to aerial parts with time. Upon prolonged exposure to 500 mg nCeO{sub 2}/L, the root antioxidant enzyme activities were significantly reduced, simultaneously increasing the root soluble protein by 204%. In addition, leaf's guaiacol peroxidase activity was enhanced with nCeO{sub 2} exposure in order to maintain cellular homeostasis.

  4. The solvent extraction of cerium from sulphate solution - mini plant trials

    International Nuclear Information System (INIS)

    Full text: The Mt. Weld deposit in Western Australia has a complex rare earth mineralisation. The rare earth phosphate minerals, which include monazite, are amenable to conventional caustic cracking followed by hydrochloric acid dissolution of the trivalent rare earths. The presence of the mineral cerianite in the ore, which is unaffected by the alkali attack, results in rejection of a considerable proportion of the cerium to the acid leach residue. The recovery of cerium from a sulphate solution, resulting from the processing of such a residue, is the subject of the current paper. The liquor treated by solvent extraction contained 63 g L-1 rare earths and the cerium to total rare earth ratio was 75%. Other impurities, including Fe and Th, totalled 2000 ppm. A solvent mixture of commercially available extractants in a low aromatic content diluent was used to extract Ce4+ selectively over the trivalent rare earths. Partial co-extraction of Fe and Th occurred but it was found that these elements were not easily stripped and therefore selective back extraction of cerium was possible. The cerium was stripped from the organic phase by hydrochloric acid and hydrogen peroxide. In continuous counter-current trials two extraction stages and three strip stages were used. In order to produce two grades of strip liquor, stripping was divided into two circuits. The first strip circuit consisting of a single stage, contained proportionally more of the trivalent rare earths. The second strip circuit, consisting of two stages, removed the remaining cerium with proportionally less of the rare earths. A bleed solvent stream was treated for removal of impurities to prevent build-up in the solvent. In the continuous counter current trials, 95% Ce4+ extraction was achieved and the Ce to total rare earth ratio was upgraded to > 99%

  5. Luminescence properties and decay kinetics of nano ZnO powder doped with cerium ions

    Energy Technology Data Exchange (ETDEWEB)

    Panda, Nihar Ranjan, E-mail: nihar@iitbbs.ac.in [Indian Institute of Technology Bhubaneswar, Bhubaneswar 751013, Orissa (India); Acharya, B.S., E-mail: bsacharya1950@gmail.com [Department of Physics, C.V. Raman College of Engineering, Bhubaneswar 752054, Orissa (India); Singh, Th. Basanta [Luminescence Dating Laboratory, Manipur University, Imphal 795003 (India); Gartia, R.K. [Department of Physics, Manipur University, Imphal 795003 (India)

    2013-04-15

    ZnO nanopowders doped with cerium ions (1.2 and 1.5 at. wt.%) were synthesized through soft solution route using ultrasound. Sonication has been found to be an effective way for doping rare earth ions like cerium into ZnO. This was confirmed from energy dispersive analysis of X-rays (EDAX) measurement. Further, optical absorption and photoluminescence (PL) measurements corroborate this finding. X-ray diffraction (XRD) studies show the increase of crystallite size and unit cell volume with doping of cerium ions. Formation of fibrous structure of ZnO:Ce was observed from the transmission electron microscopy (TEM) measurements. Although the structural measurements indicate Ce{sup 4+} ion occupying substitutional site in ZnO, PL and absorption studies confirmed the presence of Ce{sup 3+} ion in the powder. The coexistence of Ce{sup 3+} and Ce{sup 4+} ions has been explained on the basis of conversion of Ce{sup 3+} to Ce{sup 4+} in the oxidizing environment. Thermoluminescence (TL) and photo-stimulated decay of luminescence (PSDL) decay studies give an idea of various trapping levels present in the band gap of ZnO. These traps release electrons during optical stimulation to give bimolecular kinetics in nano ZnO:Ce powders. -- Highlights: ► Sonication: an effective way of incorporation of cerium ions into ZnO. ► Site dependent characteristic emission of cerium. ► Energy transfer from host lattice to cerium ions. ► Mono and bimolecular kinetics of ZnO:Ce.

  6. Ultraviolet Laser Induced Photochromic Centers in Cerium Doped Calcium-Fluoride

    Science.gov (United States)

    Pogatshnik, Gerald Joseph

    The optical excitation of the lowest 4f to 5d transition in Ce('3+):CaF(,2) using the 308 nm output of a XeCl excimer laser results in a strong coloration of the sample. The centers created by the UV laser irradiation were identified, using low temperature absorption spectroscopy, and were found to be divalent cerium ions at cubic sites in the crystal. The system exhibits photochromic properties in that the crystal can be returned to the original transparent state by illuminating it with light which is absorbed by the divalent cerium ions. The creation process for these photochromic centers involves a resonant two-photon transition from the 4f ground state of the cerium ion to the conduction band of the CaF(,2) host. The lowest 5d level of the cerium ion serves as the real intermediate state for this transition. The photoionized electron can be trapped by another trivalent cerium ion at a site of cubic symmetry. These impurity sites with O(,h) symmetry result when the charge compensator associated with the rare earth ion is somewhat removed from the cerium ion site. The charge compensator is needed to maintain charge neutrality in the crystal when a trivalent rare earth is substituted for a Ca ion in the host lattice. The absence of a local charge compensator at a Ce('3+) site with O(,h) symmetry, provides a net positive Coulombic potential, which aids in the trapping of electrons from the conduction band. The capture of an electron by a cerium ion at cubic site, changes the valence state of the ion to Ce('2+). The presence of divalent cerium, with its broad absorption bands in the visible region of the spectrum, accounts for the coloration of the crystal after illumination with UV laser light. A model for the production of the photochromic centers, based on a rate equation is presented. This model reflects the two-photon nature of the photoionization process, as well as the optical bleaching characteristics of the photochromic center, and accurately reproduces the

  7. [Laser resonance ionization spectroscopy of even-parity autoionization states of cerium atom].

    Science.gov (United States)

    Li, Zhi-ming; Zhu, Feng-rong; Zhang, Zi-bin; Ren, Xiang-jun; Deng, Hu; Zhai, Li-hua; Zhang, Li-xing

    2004-12-01

    This paper describes the investigation of even-parity autoionization states of cerium atoms by three-step three-color resonance ionization spectroscopy (RIS). Twenty-seven odd-parity highly excited levels, whose transition probability is high, were used in this research. One hundred and forty-one autoionization states were found by these channels with the third-step laser scanning in the wavelength range of 634-670 nm. The ionization probabilities of different channels, which had higher cross sections, were compared. On the basis of this, eight optimal photoionization schemes of cerium atom have been given. PMID:15828309

  8. Photocatalytic action of cerium molybdate and iron-titanium oxide hollow nanospheres on Escherichia coli

    International Nuclear Information System (INIS)

    This study is focused on the production of hollow nanospheres that reveal antibacterial action. Cerium molybdate and iron-titanium oxide hollow nanospheres with a diameter of 175 ± 15 and 221 ± 10 nm, respectively, were synthesized using emulsion polymerization and the sol–gel process. Their morphology characterization was accomplished using scanning electron microscopy. Their antibacterial action was examined on pure culture of Escherichia coli considering the loss of their viability. Both hollow nanospheres presented photocatalytic action after illumination with blue–black light, but those of cerium molybdate also demonstrated photocatalytic action in the dark. Therefore, the produced nanospheres can be used for antibacterial applications.

  9. METHOD OF SEPARATING TETRAVALENT PLUTONIUM VALUES FROM CERIUM SUB-GROUP RARE EARTH VALUES

    Science.gov (United States)

    Duffield, R.B.; Stoughton, R.W.

    1959-02-01

    A method is presented for separating plutonium from the cerium sub-group of rare earths when both are present in an aqueous solution. The method consists in adding an excess of alkali metal carbonate to the solution, which causes the formation of a soluble plutonium carbonate precipitate and at the same time forms an insoluble cerium-group rare earth carbonate. The pH value must be adjusted to bctween 5.5 and 7.5, and prior to the precipitation step the plutonium must be reduced to the tetravalent state since only tetravalent plutonium will form the soluble carbonate complex.

  10. Cerium Binding Activity of Pectins Isolated from the Seagrasses Zostera marina and Phyllospadix iwatensis

    OpenAIRE

    Valeri Kovalev; Maxim Khotimchenko; Yuri Khotimchenko; Elena Khozhaenko

    2012-01-01

    Cerium binding activity of three different water soluble pectin compounds of different origin was studied in a batch sorption system. The Langmuir, Freundlich and BET sorption models were adopted to describe the binding reactions between metal ions and pectin molecules. The Langmuir model provided the best fit. Within the pH range from 4.0 to 6.0, the largest amount of the cerium ions was bound by pectin isolated from the seagrass Phylospadix iwatensis in comparison to pectin extracted from t...

  11. Synthesis and characterization of two dimensional metal organic framework of cerium with tetraaza macrocyclic

    Energy Technology Data Exchange (ETDEWEB)

    Bt Safiin, Nurul Atikah; Yarmo, Ambar; Yamin, Bohari M. [School of Chemical Science and Food Technology. Faculty Science and Technology, Universiti Kebangsaan Malaysia, 43600 Bangi, Selangor Darul Ehsan (Malaysia)

    2013-11-27

    A two dimensional metal organic framework containing cerium sufate layers and ethylenediaminium between layers was obtained by refluxing the mixture of cerium sulphate and 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-7, 14-diene bromide. The complex was characterized by infrared spectroscopy and microelemental analysis. X-ray study showed that the complex adopts eleven coordination environments about the central atom. Thermogravimetric study showed the removal of water molecules at about 70°C followed by a gradual mass loss until the whole structure collapsed at about 400°C.

  12. Thin film growth of epitaxial gadolinium oxide, gadolinium yttrium oxide, and gadolinium cerium oxide by electrodeposition

    International Nuclear Information System (INIS)

    Thin films of gadolinium oxide, gadolinium yttrium oxide, and gadolinium cerium oxide were electrodeposited from non-aqueous baths. The films were on the order of 15 nm thick, and were grown epitaxially on textured nickel-tungsten substrates. The effect of deposition rate, annealing temperature and secondary metals on crystallinity and crystal orientation was investigated by X-ray diffraction and transmission electron microscopy. Slower rates, higher temperatures and low concentrations of yttrium improve the crystallinity of gadolinium oxide films, whereas the introduction of cerium induced polycrystallinity.

  13. A corrosion resistant cerium oxide based coating on aluminum alloy 2024 prepared by brush plating

    International Nuclear Information System (INIS)

    Cerium oxide based coatings were prepared on AA2024 Al alloy by brush plating. The characteristic of this technology is that hydrogen peroxide, which usually causes the plating solution to be unstable, is not necessary in the plating electrolyte. The coating showed laminated structures and good adhesive strength with the substrate. X-ray diffraction and X-ray photoelectron spectroscopy analysis showed that the coatings were composed of Ce(III) and Ce(IV) oxides. The brush plated coatings on Al alloys improved corrosion resistance. The influence of plating parameters on structure and corrosion resistance of the cerium oxide based coating was studied.

  14. Plasma-electrolytic formation of cerium-containing surface structures on titanium and aluminum

    International Nuclear Information System (INIS)

    The possibility of obtaining cerium-containing structures on aluminum and titanium by the plasma-electrolytic method with the use of aqueous solutions of electrolytes containing Ce3+ polyphosphate complexes was demonstrated. The amount of cerium in the films obtained depended on the molar ratio n [polyphosphate]/[Ce3+] in the electrolyte. The films contained crystalline CePO4. The growth of films on titanium was characterized by the formation of secondary layers by the mechanism involving the appearance of new phase nuclei followed by their expansion

  15. Thin film growth of epitaxial gadolinium oxide, gadolinium yttrium oxide, and gadolinium cerium oxide by electrodeposition

    Energy Technology Data Exchange (ETDEWEB)

    Mann, Jonathan R., E-mail: jonathan.mann@nrel.gov; Bhattacharya, Raghu N.

    2010-10-29

    Thin films of gadolinium oxide, gadolinium yttrium oxide, and gadolinium cerium oxide were electrodeposited from non-aqueous baths. The films were on the order of 15 nm thick, and were grown epitaxially on textured nickel-tungsten substrates. The effect of deposition rate, annealing temperature and secondary metals on crystallinity and crystal orientation was investigated by X-ray diffraction and transmission electron microscopy. Slower rates, higher temperatures and low concentrations of yttrium improve the crystallinity of gadolinium oxide films, whereas the introduction of cerium induced polycrystallinity.

  16. Synthesis and characterization of platinum supported on alumina doped with cerium catalyst

    International Nuclear Information System (INIS)

    The synthesis and characterization of gamma-alumina doped with cerium as platinum support for the automobile exhaust catalyst are described. Platinum/alumina/ceria catalyst were prepared by impregnation of hexachloroplatinic acid and sintered at 500 degree Celsius to obtain metal dispersions of 1.0 wt%. Catalyst distribution inside the powder and the effects of the addition of cerium to alumina were analyzed by the scanning electron microscopy (SEM) and x-ray fluorescence spectroscopy (XRF). The results showed that the alumina - supported catalysts contained well dispersion of the noble metal

  17. Electronic interaction in oxide copper-cerium catalysts according to exoemission data

    International Nuclear Information System (INIS)

    The electronic properties of the oxide copper-cerium catalysts with different copper content are studied through the exoemission methods. It is shown, that the introduction of the copper increases the CeO2 emission activity and the number of the electrons, emitted from the catalysts surface, as compared to the surface of the CeO2 and CuO initial oxides. It is concluded, that the event of synergism in the exoemission from the studied systems surface is conditioned through the electronic interactions, including the electronic transitions on the cerium oxide - copper oxide boundary

  18. A corrosion resistant cerium oxide based coating on aluminum alloy 2024 prepared by brush plating

    Energy Technology Data Exchange (ETDEWEB)

    Tang Junlei; Han Zhongzhi [School of Materials Science and Engineering, Beijing University of Chemical Technology, Beijing 100029 (China); Zuo Yu, E-mail: zuoy@mail.buct.edu.cn [School of Materials Science and Engineering, Beijing University of Chemical Technology, Beijing 100029 (China); Tang Yuming [School of Materials Science and Engineering, Beijing University of Chemical Technology, Beijing 100029 (China)

    2011-01-15

    Cerium oxide based coatings were prepared on AA2024 Al alloy by brush plating. The characteristic of this technology is that hydrogen peroxide, which usually causes the plating solution to be unstable, is not necessary in the plating electrolyte. The coating showed laminated structures and good adhesive strength with the substrate. X-ray diffraction and X-ray photoelectron spectroscopy analysis showed that the coatings were composed of Ce(III) and Ce(IV) oxides. The brush plated coatings on Al alloys improved corrosion resistance. The influence of plating parameters on structure and corrosion resistance of the cerium oxide based coating was studied.

  19. Evaluation of Antiproliferative Potential of Cerium Oxide Nanoparticles on HeLa Human Cervical Tumor Cell

    Directory of Open Access Journals (Sweden)

    Zoriţa Diaconeasa

    2015-05-01

    Full Text Available Cerium oxide nanoparticles (CeO2 nanoparticles as nanomaterials have promising biomedical applications. In this paper, the cytotoxicity induced by CONPs human cervical tumor cells was investigated. Cerium oxide nanoparticles were synthesized using the precipitation method. The nanoparticles were found to inhibit the proliferation of HeLa human cervical tumor cells in a dose dependent manner but did not showed to be cytotoxic as analyzed by MTT assay. The administrated treatment decreased the HeLa cell viability cells from 100% to 65% at the dose of 100 μg/mL.

  20. XPS study of cerium conversion coating on the anodized 2024 aluminum alloy

    International Nuclear Information System (INIS)

    Cerium-rich conversion coating was deposited on anodized aluminum alloy 2024 in a solution containing Ce(NO3)3. X-ray photoelectron spectroscopy (XPS) was used as the analysis method. The composition of the Ce conversion coating deposited on the anodized 2024 alloy was investigated using this method. It was revealed that the coating predominately consisted of three-valent state cerium compound. Some of the CeIII was oxidized to CeIV in the outer layer coating

  1. Synthesis and characterization of two dimensional metal organic framework of cerium with tetraaza macrocyclic

    International Nuclear Information System (INIS)

    A two dimensional metal organic framework containing cerium sufate layers and ethylenediaminium between layers was obtained by refluxing the mixture of cerium sulphate and 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-7, 14-diene bromide. The complex was characterized by infrared spectroscopy and microelemental analysis. X-ray study showed that the complex adopts eleven coordination environments about the central atom. Thermogravimetric study showed the removal of water molecules at about 70°C followed by a gradual mass loss until the whole structure collapsed at about 400°C

  2. Decontamination of alpha contaminated metallic waste by cerium IV redox process

    International Nuclear Information System (INIS)

    Decontamination of alpha contaminated metallic waste is an important aspect in the management of waste generated during dismantling and decommissioning of nuclear facilities. Present work on cerium redox process targets decontamination of alpha contaminated metallic waste till it qualifies for the non alpha waste category for disposal in near surface disposal facility. Recovery of the alpha radio nuclides and cerium from aqueous secondary waste streams was also studied deploying solvent extraction process and established. The alpha-lean secondary waste stream has been immobilised in cement based matrix for final disposal. (author)

  3. Dissociation of outer membrane for Escherichia coli cell caused by cerium nitrate

    Institute of Scientific and Technical Information of China (English)

    陈爱美; 施庆珊; 冯劲; 欧阳友生; 陈仪本; 谭绍早

    2010-01-01

    The biological effect of cerium nitrate on the outer membrane(OM) of Escherichia coli(E.coli) cell was studied,and the antim-icrobial mechanism of rare earth elements was explored.The antimicrobial effect of cerium nitrate on E.coli cell was valued by plate count method,and the morphology change of E.coli cell was observed with scanning electron microscopy(SEM) and transmission electron microscopy(TEM).The results showed that the E.coli cell suspension was flocculated when the concentration of Ce(NO3)3?6H2O...

  4. Comparative Study of Magnetic Instabilities in Cerium Compounds

    International Nuclear Information System (INIS)

    The variety of new phases and physical phenomena discovered in intermetallic compounds containing Rare Earths or Actinides has motivated, during the last four decades, the sustained study of their magnetic phase diagrams.The current interest is focused on the investigation of the region of the phase diagram where the magnetic order of Cerium, Ytterbium and Uranium based systems is destabilized.In this region different behaviours have been detected, such as non conventional superconductivity and the anomalous dependencies of the thermal, magnetic and transport properties at very low temperatures, associated to non-Fermi liquid behaviour.A simple model, the Doniach diagram, has guided the interpretation of the destabilization of the magnetic order in the previously mentioned systems.However, most of the systems that have been studied so far cannot be described within this model.This fact has motivated the development of a phenomenological classification of phase diagrams that has been mostly applied to cerium based compounds.This classification defines three types of phase diagrams, that can be distinguished by the way in which the magnetic transition is suppressed when a control parameter (such as doping or pressure) is driven towards its critical value.Within this scenario, we study the suppression of the antiferromagnetic order of the intermetallic compounds CeIn3, CeRh2Si2 and CePd2Al3 as a function of Ce-ligand alloying.The resulting systems, CeIn3-xSnx, Ce(CuxRh1-x)2Si2 and CePd2-xNixAl3, present different crystalline structures and the effects produced by the alloying process are different in each case.We analyse the resulting magnetic phase diagrams, and compare them with the above mentioned phenomenological classification.With such a purpose, we study in detail the region in which the magnetic instability takes place, in the proximity of the respective critical concentrations.Taking into account both our results and those reported in the literature, we

  5. Fate of cerium dioxide nanoparticles in endothelial cells: exocytosis

    International Nuclear Information System (INIS)

    Although cytotoxicity and endocytosis of nanoparticles have been the subject of numerous studies, investigations regarding exocytosis as an important mechanism to reduce intracellular nanoparticle accumulation are rather rare and there is a distinct lack of knowledge. The current study investigated the behavior of human microvascular endothelial cells to exocytose cerium dioxide (CeO2) nanoparticles (18.8 nm) by utilization of specific inhibitors [brefeldin A; nocodazole; methyl-β-cyclodextrin (MβcD)] and different analytical methods (flow cytometry, transmission electron microscopy, inductively coupled plasma mass spectrometry). Overall, it was found that endothelial cells were able to release CeO2 nanoparticles via exocytosis after the migration of nanoparticle containing endosomes toward the plasma membrane. The exocytosis process occurred mainly by fusion of vesicular membranes with plasma membrane resulting in the discharge of vesicular content to extracellular environment. Nevertheless, it seems to be likely that nanoparticles present in the cytosol could leave the cells in a direct manner. MβcD treatment led to the strongest inhibition of the nanoparticle exocytosis indicating a significant role of the plasma membrane cholesterol content in the exocytosis process. Brefeldin A (inhibitor of Golgi-to-cell-surface-transport) caused a higher inhibitory effect on exocytosis than nocodazole (inhibitor of microtubules). Thus, the transfer from distal Golgi compartments to the cell surface influenced the exocytosis process of the CeO2 nanoparticles more than the microtubule-associated transport. In conclusion, endothelial cells, which came in contact with nanoparticles, e.g., after intravenously applied nano-based drugs, can regulate their intracellular nanoparticle amount, which is necessary to avoid adverse nanoparticle effects on cells

  6. Thermoluminescence of cerium and terbium -doped calcium pyrophosphate

    Energy Technology Data Exchange (ETDEWEB)

    Roman L, J.; Cruz Z, E. [UNAM, Instituto de Ciencias Nucleares, Circuito Exterior, Ciudad Universitaria, 04510 Mexico D. F. (Mexico); Lozano R, I. B.; Diaz G, J. A. I., E-mail: jesus.roman@nucleares.unam.mx [IPN, Centro de Investigacion en Ciencia Aplicada y Tecnologia Avanzada, Av. Legaria No. 694, 11500 Mexico D. F. (Mexico)

    2015-10-15

    The aim of this work is to report the thermoluminescence (Tl) response of Calcium Pyrophosphate phosphor doped with Cerium and Terbium impurities (Ca{sub 2}P{sub 2}O{sub 7}:Ce{sup 3+},Tb{sup 3+}). The phosphors were synthesized using the co-precipitation method and annealed at 900 degrees C by two hours for obtain the β phase. The intentional doping with Ce and Tb ions was 1 at.% and 0.1 at.%, whereas in the EDS results the concentration of impurities was 0.39 at.% and 0.05 at.%, respectively. The superficial morphology of phosphor is mainly composed by thin wafers of different size. All samples were exposed to gamma rays from {sup 60}Co in the Gammacell-200 irradiator. The Tl response of the phosphor was measured from Rt up to 350 degrees C and under nitrogen atmosphere in a Harshaw TLD 3500 reader. The glow curves of the Ca{sub 2}P{sub 2}O{sub 7}:Ce{sup 3+},Tb{sup 3+} powders showed a broad intense Tl peak centered at 165 degrees C and a shoulder at approximate 260 degrees C was observed. A linear Tl response in the range of absorbed dose of 0.2 to 10 Gy was obtained. Tl glow curves were analyzed using the initial rise (IR)and computerized glow curve deconvolution methods to evaluate the kinetics parameters such as activation energy (E), frequency factor (s) and kinetic order (b). (Author)

  7. Fate of cerium dioxide nanoparticles in endothelial cells: exocytosis

    Energy Technology Data Exchange (ETDEWEB)

    Strobel, Claudia, E-mail: Claudia.Strobel@med.uni-jena.de [Jena University Hospital – Friedrich Schiller University Jena, Department of Experimental Radiology, Institute of Diagnostic and Interventional Radiology (Germany); Oehring, Hartmut [Jena University Hospital – Friedrich Schiller University Jena, Institute of Anatomy II (Germany); Herrmann, Rudolf [University of Augsburg, Department of Physics (Germany); Förster, Martin [Jena University Hospital – Friedrich Schiller University Jena, Department of Internal Medicine I, Division of Pulmonary Medicine and Allergy/Immunology (Germany); Reller, Armin [University of Augsburg, Department of Physics (Germany); Hilger, Ingrid, E-mail: ingrid.hilger@med.uni-jena.de [Jena University Hospital – Friedrich Schiller University Jena, Department of Experimental Radiology, Institute of Diagnostic and Interventional Radiology (Germany)

    2015-05-15

    Although cytotoxicity and endocytosis of nanoparticles have been the subject of numerous studies, investigations regarding exocytosis as an important mechanism to reduce intracellular nanoparticle accumulation are rather rare and there is a distinct lack of knowledge. The current study investigated the behavior of human microvascular endothelial cells to exocytose cerium dioxide (CeO{sub 2}) nanoparticles (18.8 nm) by utilization of specific inhibitors [brefeldin A; nocodazole; methyl-β-cyclodextrin (MβcD)] and different analytical methods (flow cytometry, transmission electron microscopy, inductively coupled plasma mass spectrometry). Overall, it was found that endothelial cells were able to release CeO{sub 2} nanoparticles via exocytosis after the migration of nanoparticle containing endosomes toward the plasma membrane. The exocytosis process occurred mainly by fusion of vesicular membranes with plasma membrane resulting in the discharge of vesicular content to extracellular environment. Nevertheless, it seems to be likely that nanoparticles present in the cytosol could leave the cells in a direct manner. MβcD treatment led to the strongest inhibition of the nanoparticle exocytosis indicating a significant role of the plasma membrane cholesterol content in the exocytosis process. Brefeldin A (inhibitor of Golgi-to-cell-surface-transport) caused a higher inhibitory effect on exocytosis than nocodazole (inhibitor of microtubules). Thus, the transfer from distal Golgi compartments to the cell surface influenced the exocytosis process of the CeO{sub 2} nanoparticles more than the microtubule-associated transport. In conclusion, endothelial cells, which came in contact with nanoparticles, e.g., after intravenously applied nano-based drugs, can regulate their intracellular nanoparticle amount, which is necessary to avoid adverse nanoparticle effects on cells.

  8. Effects of Cerium Oxide Nanoparticles on Sorghum Plant Traits

    Science.gov (United States)

    Mu, L.; Chen, Y.; Darnault, C. J. G.; Rauh, B.; Kresovich, S.; Korte, C.

    2015-12-01

    Nanotechnology and nanomaterials are considered as the development of the modern science. However, besides with that wide application, nanoparticles arouse to the side effects on the environment and human health. As the catalyst of ceramics and fuel industry, Cerium (IV) oxide nanoparticles (CeO2 NPs) can be found in the environment following their use and life-cycle. Therefore, it is critical to assess the potential effects that CeO2 NPs found in soils may have on plants. In this study, CeO2 NPs were analyzed for the potential influence on the sorghum [Sorghum bicolor (L.) Moench] (Reg. no. 126) (PI 154844) growth and traits. The objectives of this research were to determine whether CeO2 NPs impact the sorghum germination and growth characteristics. The sorghum was grown in the greenhouse located at Biosystems Research Complex, Clemson University under different CeO2 NPs treatments (0mg; 100mg; 500mg; 1000mg CeO2 NPs/Kg soil) and harvested around each month. At the end of the each growing period, above ground vegetative tissue was air-dried, ground to 2mm particle size and compositional traits estimated using near-infrared spectroscopy. Also, the NPK value of the sorghum tissue was tested by Clemson Agriculture Center. After the first harvest, the result showed that the height of above ground biomass under the nanoparticles stress was higher than that of control group. This difference between the control and the nanoparticles treatments was significant (F>F0.05; LSD). Our results also indicated that some of the compositional traits were impacted by the different treatments, including the presence and/or concentrations of the nanoparticles.

  9. Contribution to research on the metabolism of fission product. Studies on the physico-chemical state and the metabolic fate of radio-cerium solution

    International Nuclear Information System (INIS)

    This paper describes a study of the physico-chemical state of radio-cerium in dilute solutions on the tracer scale, as a function of the pH of the solution. The way in which this radioelement is transported in the blood is studied in vitro and in vivo, with reference to the ionic or colloidal state of the radio-cerium used. The distribution of cerium amongst the various components of the blood is studied by a new method of blood fractionation and by paper electrophoresis. Evidence of a cerium globulin connection is shown in the case of ionic cerium. A study of the initial distribution of radio-cerium in rats, after intravenous administration of ionic or colloidal solutions, shows considerable differences according to the physico-chemical state of the cerium injected. (author)

  10. Hydride precipitation and its influence on mechanical properties of notched and unnotched Zircaloy-4 plates

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Zhiyang, E-mail: zw603@uowmail.edu.au [Faculty of Engineering, University of Wollongong, Northfields Avenue, Wollongong, NSW 2522 (Australia); The Bragg Institute, Australian Nuclear Science and Technology Organisation, New Illawarra Road, Lucas Heights, NSW 2234 (Australia); Garbe, Ulf [The Bragg Institute, Australian Nuclear Science and Technology Organisation, New Illawarra Road, Lucas Heights, NSW 2234 (Australia); Li, Huijun [Faculty of Engineering, University of Wollongong, Northfields Avenue, Wollongong, NSW 2522 (Australia); Harrison, Robert P.; Toppler, Karl [The Institute of Materials Engineering, Australian Nuclear Science and Technology Organisation, New Illawarra Road, Lucas Heights, NSW 2234 (Australia); Studer, Andrew J. [The Bragg Institute, Australian Nuclear Science and Technology Organisation, New Illawarra Road, Lucas Heights, NSW 2234 (Australia); Palmer, Tim [The Institute of Materials Engineering, Australian Nuclear Science and Technology Organisation, New Illawarra Road, Lucas Heights, NSW 2234 (Australia); Planchenault, Guillaume [Electricite De France, 6 Avenue Montaigne, 93192 Noisy Le Grand Cédex (France)

    2013-05-15

    The hydride formation and its influence on the mechanical performance of hydrided Zircaloy-4 plates containing different hydrogen contents were studied at room temperature. For the unnotched plate samples with the hydrogen contents ranging from 25 to 850 wt. ppm, the hydrides exerted an insignificant effect on the tensile strength, while the ductility was severely degraded with increasing hydrogen content. The fracture mode and degree of embrittlement were strongly related to the hydrogen content. When the hydrogen content reached a level of 850 wt. ppm, the plate exhibited negligible ductility, resulting in almost completely brittle behavior. For the hydrided notched plate, the tensile stress concentration associated with the notch tip facilitated the hydride accumulation at the region near the notch tip and the premature crack propagation through the hydride fracture during hydriding. The final brittle through-thickness failure for this notched sample was mainly attributed to the formation of a continuous hydride network on the thickness section and the obtained very high hydrogen concentration (estimated to be 1965 wt. ppm)

  11. Cracking in hydride blisters in Zr-2.5Nb pressure tubes

    International Nuclear Information System (INIS)

    When the pressure tubes contact to the calandria tubes in the CANDU reactor, temperature gradient in the Zr-2.5Nb pressure tube causes the thermal diffusion of hydrogen and formation of hydride blisters. This surface shape change is a result of the volume expansion associated with the transformation from pressure tube matrix to δ-phase hydride. Cracking in the hydride blisters may cause a direct failure of pressure tubes or develope to the delayed hydride cracking. The Zr-2.5Nb pressure tube specimen are hydrided by an electrolytic method and homogenized considering the temperature and time of hydrogen diffusion. The hydride blisters are formed on the outer surface of the specimen by a thermal diffusion between a heat bath maintained at the temperature of 415 deg C and an aluminum cold finger cooled with the flowing water of 15 deg C. An optical microscopy and 3-dimensional profilometry were used to characterize the hydride blisters with different hydrogen concentrations and thermal diffusion times. It reveals higher possibility of cracking for higher hydrogen concentration and longer time for thermal diffusion. The mechanism of cracking in the hydride blister is discussed

  12. Hydride trapping for AAS: Complex analytical problems can be handled with a simple instrumentation

    Czech Academy of Sciences Publication Activity Database

    Dědina, Jiří; de Moraes, D. P.; Dessuy, M. B.; Kratzer, Jan; Matoušek, Tomáš; de Moraes Flores, E. M.; Vale, M. G. R.

    Ankara Üniversitesi, 2011. [National Spectroscopy Congress /12./. 18.05.2011-22.05.2011, Antalya] R&D Projects: GA ČR GA203/09/1783 Institutional research plan: CEZ:AV0Z40310501 Keywords : atomic absorption spectrometry * hydride generation * hydride trapping Subject RIV: CB - Analytical Chemistry, Separation

  13. Absorption kinetics and hydride formation in magnesium films: Effect of driving force revisited

    International Nuclear Information System (INIS)

    Electrochemical hydrogen permeation measurements and in situ gas-loading X-ray diffraction measurements were performed on polycrystalline Mg films. Hydrogen diffusion constants, the hydride volume content and the in-plane stress were determined for different values of driving forces at 300 K. For α-Mg–H, a hydrogen diffusion constant of DHMg=7(±2)·10-11 m2 s−1 was determined. For higher concentrations, different kinetic regimes with reduced apparent diffusion constants DHtot were found, depending on the driving force, decreasing to about DHtot = 10−18 m2 s−1. This lowest measured diffusion constant is two orders of magnitude larger than that of bulk β-MgH2, and the difference is ascribed to a contribution from a fast diffusion along grain boundaries. The different kinetics regimes are attributed to the spatial distribution of hydrides. A heterogeneous hydride nucleation and growth model is suggested that is based on hemispherical hydrides spatially distributed according to the nuclei densities expressed as a function of the driving force. The model allows us to qualitatively explain the complex stress development, the different diffusion regimes and the blocking-layer thickness. As the blocking-layer thickness inversely scales with the driving force, small driving forces allow the hydriding of large film volume fractions. Maximum stress situations occur for hydride distances reaching four times the hydride radius and for hydride distances equaling the film thickness

  14. Hydride precipitation crack propagation in zircaloy cladding during a decreasing temperature history

    International Nuclear Information System (INIS)

    An assessment of safety, design, and cost tradeoff issues for short (ten to fifty years) and longer (fifty to hundreds of years) interim dry storage of spent nuclear fuel in Zircaloy rods shall address potential failures of the Zircaloy cladding caused by the precipitation response of zirconium hydride platelets. To perform such assessment analyses rigorously and conservatively will be necessarily complex and difficult. For Zircaloy cladding, a model for zirconium hydride induced crack propagation velocity was developed for a decreasing temperature field and for hydrogen, temperature, and stress dependent diffusive transport of hydrogen to a generic hydride platelet at a crack tip. The development of the quasi-steady model is based on extensions of existing models for hydride precipitation kinetics for an isolated hydride platelet at a crack tip. An instability analysis model of hydride-crack growth was developed using existing concepts in a kinematic equation for crack propagation at a constant thermodynamic crack potential subject to brittle fracture conditions. At the time an instability is initiated, the crack propagation is no longer limited by hydride growth rate kinetics, but is then limited by stress rates. The model for slow hydride-crack growth will be further evaluated using existing available data. (authors)

  15. Experiments on hadronic-atom x-ray intensities of hydrides and deuterides

    Energy Technology Data Exchange (ETDEWEB)

    Wiegand, C.E.; Lum, G.K.; Godfrey, G.L.

    1977-04-01

    Kaonic-atom x-ray intensities of elements Z = 3, 6, 8, 11, and 20 were significantly reduced when the elements were in hydride form. The ratios I (ZH/sub m/)/I (Z) have a noticeable Z dependence. Deuterides of C and O showed slightly less x-ray emission than their hydride counterparts.

  16. Thermal and mechanical properties of zirconium hydrides with various hafnium contents

    International Nuclear Information System (INIS)

    Zirconium (Zr) hydride is currently expected as a neutron shield material for fast reactors. In order to evaluate safety and economic efficiency of the nuclear reactor, the thermal and mechanical properties of the hydride should be understood. In addition, since chemical properties of Zr and hafnium (Hf) are quite similar, Zr contains a few percent Hf generally. Therefore, it is very important to evaluate the effect of Hf content on the properties of Zr hydride. In the present study, fine bulk samples of δ-phase Zr hydrides with various Hf contents were prepared and their thermal and mechanical properties were investigated. We examined the phase states and the microstructure of the hydrides by means of X-ray diffraction and SEM/EDX analyses. In the temperature range from room temperature to 673 K, the heat capacity and the thermal diffusivity of the hydrides were measured and the thermal conductivity was evaluated. The Vickers hardness and the sound velocity of the hydrides were measured at room temperature, and the elastic modulus was calculated from the measured sound velocity. The effects of temperature and Hf content on the properties of Zr hydrides were studied. (author)

  17. Hydride precipitation and its influence on mechanical properties of notched and unnotched Zircaloy-4 plates

    International Nuclear Information System (INIS)

    The hydride formation and its influence on the mechanical performance of hydrided Zircaloy-4 plates containing different hydrogen contents were studied at room temperature. For the unnotched plate samples with the hydrogen contents ranging from 25 to 850 wt. ppm, the hydrides exerted an insignificant effect on the tensile strength, while the ductility was severely degraded with increasing hydrogen content. The fracture mode and degree of embrittlement were strongly related to the hydrogen content. When the hydrogen content reached a level of 850 wt. ppm, the plate exhibited negligible ductility, resulting in almost completely brittle behavior. For the hydrided notched plate, the tensile stress concentration associated with the notch tip facilitated the hydride accumulation at the region near the notch tip and the premature crack propagation through the hydride fracture during hydriding. The final brittle through-thickness failure for this notched sample was mainly attributed to the formation of a continuous hydride network on the thickness section and the obtained very high hydrogen concentration (estimated to be 1965 wt. ppm)

  18. Degradation of nitrobenzene using titania photocatalyst co-doped with nitrogen and cerium under visible light illumination

    International Nuclear Information System (INIS)

    A type of nitrogen and cerium co-doped titania photocatalyst, which could degrade nitrobenzene under visible light irradiation, was prepared by the sol-gel route. Titanium isopropoxide, ammonium nitrate, and cerium nitrate were used as the sources of titanium, nitrogen, and cerium, respectively. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV-vis diffusive reflectance spectroscopy (DRS), scanning electron microscopy (SEM), and N2 adsorption-desorption isotherm were employed to characterize the as-prepared photocatalyst. The degradation of nitrobenzene under visible light illumination was taken as probe reaction to evaluate the photoactivity of the co-doped photocatalyst. The commercial TiO2 photocatalyst (Degussa P25), which was thought as a high active photocatalyst, was chosen as standard photocatalyst to contrast the photoactivity of the nitrogen and cerium co-doped titania photocatalyst. The results showed that the photocatalytic performance of the nitrogen and cerium co-doped titania was related with the calcination temperature and the component. The nitrogen atoms were incorporated into the crystal of titania and could narrow the band gap energy. The doping cerium atoms existed in the forms of Ce2O3 and dispersed on the surface of TiO2. The improvement of the photocatalytic activity was ascribed to the synergistic effects of the nitrogen and cerium co-doping

  19. Cerium Oxide Nanoparticles and Bulk Cerium Oxide Leading to Different Physiological and Biochemical Responses in Brassica rapa.

    Science.gov (United States)

    Ma, Xingmao; Wang, Qiang; Rossi, Lorenzo; Zhang, Weilan

    2016-07-01

    Cerium oxide nanoparticles (CeO2NPs) have been incorporated into many commercial products, and their potential release into the environment through the use and disposal of these products has caused serious concerns. Despite the previous efforts and rapid progress on elucidating the environmental impact of CeO2NPs, the long-term impact of CeO2NPs to plants, a key component of the ecosystem, is still not well understood. The potentially different impact of CeO2NPs and their bulk counterparts to plants is also unclear. The main objectives of this study were (1) to investigate whether continued irrigation with solutions containing different concentrations of CeO2NPs (0, 10, and 100 mg/L) would induce physiological and biochemical adjustments in Brassica rapa in soil growing conditions and (2) to determine whether CeO2NPs and bulk CeO2 particles exert different impacts on plants. The results indicated that bulk CeO2 at 10 and 100 mg/L enhanced plant biomass by 28% and 35%, respectively, while CeO2NPs at equivalent concentrations did not. While the bulk CeO2 treatment resulted in significantly higher concentrations of hydrogen peroxide (H2O2) in plant tissues at the vegetative stage, CeO2NPs led to significantly higher H2O2 levels in plant tissues at the floral stage. The activity of superoxide dismutase (SOD) in Brassica rapa also displayed a growth-stage dependent response to different sizes of CeO2 while catalase (CAT) activity was not affected by either size of CeO2 throughout the life cycle of Brassica rapa. Altogether, the results demonstrated that plant responses to CeO2 exposure varied with the particle sizes and the growth stages of plants. PMID:26691446

  20. Mathematical modeling of the nickel/metal hydride battery system

    Energy Technology Data Exchange (ETDEWEB)

    Paxton, B K [Univ. of California, Berkeley, CA (United States). Dept. of Chemical Engineering

    1995-09-01

    A group of compounds referred to as metal hydrides, when used as electrode materials, is a less toxic alternative to the cadmium hydroxide electrode found in nickel/cadmium secondary battery systems. For this and other reasons, the nickel/metal hydride battery system is becoming a popular rechargeable battery for electric vehicle and consumer electronics applications. A model of this battery system is presented. Specifically the metal hydride material, LaNi{sub 5}H{sub 6}, is chosen for investigation due to the wealth of information available in the literature on this compound. The model results are compared to experiments found in the literature. Fundamental analyses as well as engineering optimizations are performed from the results of the battery model. In order to examine diffusion limitations in the nickel oxide electrode, a ``pseudo 2-D model`` is developed. This model allows for the theoretical examination of the effects of a diffusion coefficient that is a function of the state of charge of the active material. It is found using present data from the literature that diffusion in the solid phase is usually not an important limitation in the nickel oxide electrode. This finding is contrary to the conclusions reached by other authors. Although diffusion in the nickel oxide active material is treated rigorously with the pseudo 2-D model, a general methodology is presented for determining the best constant diffusion coefficient to use in a standard one-dimensional battery model. The diffusion coefficients determined by this method are shown to be able to partially capture the behavior that results from a diffusion coefficient that varies with the state of charge of the active material.

  1. Cathodic electrodeposition of cerium based oxides on carbon steel from concentrated cerium nitrate. Part II: Influence of electrodeposition parameters and of the addition of PEG

    Energy Technology Data Exchange (ETDEWEB)

    Hamlaoui, Y. [Laboratoire d' Etudes des Materiaux en Milieux Agressifs (LEMMA), Pole Sciences et Technologie, Universite de La Rochelle, Avenue Michel Crepeau, 17042 La Rochelle Cedex 1 (France); Institut des Sciences et Sciences de l' Ingenieur, Centre Universitaire de Souk-Ahras, BP 1553, 41000 Souk-Ahras (Algeria); Tifouti, L. [Laboratoire de Genie de l' Environnement, Universite Badji Mokhtar, BP 1223, 23020, El Hadjar-Annaba (Algeria); Remazeilles, C. [Laboratoire d' Etudes des Materiaux en Milieux Agressifs (LEMMA), Pole Sciences et Technologie, Universite de La Rochelle, Avenue Michel Crepeau, 17042 La Rochelle Cedex 1 (France); Pedraza, F., E-mail: fpedraza@univ-lr.fr [Laboratoire d' Etudes des Materiaux en Milieux Agressifs (LEMMA), Pole Sciences et Technologie, Universite de La Rochelle, Avenue Michel Crepeau, 17042 La Rochelle Cedex 1 (France)

    2010-03-15

    The mechanisms of formation of cerium based oxides on carbon steel by cathodic electrodeposition from relatively concentrated cerium nitrate solutions were investigated in a previous work (Part I). It was shown that some corrosion products developed on the steel upon and soon after coating, thereby suggesting the films were not protective. This work (Part II) focuses on the influence of various elaboration parameters on the composition and morphology of the deposits likely to improve the corrosion resistance of carbon steel. It will be shown that an increase of the precursor concentration increases the Ce(OH){sub 3} content of the deposits and brings about larger crystallite sizes at low to moderate applied current densities. As a result, the formation of the carbonated green rust corrosion product is not hindered. The kinetics of formation of the film follows a polynomial law in which concurrent deposition and dissolution steps are combined. However, an increase of the deposition time results in a reduced content of Ce(OH){sub 3} in the layers, hence in an evolution of the colour of the deposits. Similarly, the increase of the temperature of the bath brings about significant modifications of the surface morphology, of the crystallite size and of the content of oxygen vacancies that are suspected not to confer adequate protection. In contrast, the addition of 10 g L{sup -1} of PEG to the 0.1 M cerium nitrate solutions will be shown to inhibit the development of the carbonated green rust.

  2. Cathodic electrodeposition of cerium based oxides on carbon steel from concentrated cerium nitrate. Part II: Influence of electrodeposition parameters and of the addition of PEG

    International Nuclear Information System (INIS)

    The mechanisms of formation of cerium based oxides on carbon steel by cathodic electrodeposition from relatively concentrated cerium nitrate solutions were investigated in a previous work (Part I). It was shown that some corrosion products developed on the steel upon and soon after coating, thereby suggesting the films were not protective. This work (Part II) focuses on the influence of various elaboration parameters on the composition and morphology of the deposits likely to improve the corrosion resistance of carbon steel. It will be shown that an increase of the precursor concentration increases the Ce(OH)3 content of the deposits and brings about larger crystallite sizes at low to moderate applied current densities. As a result, the formation of the carbonated green rust corrosion product is not hindered. The kinetics of formation of the film follows a polynomial law in which concurrent deposition and dissolution steps are combined. However, an increase of the deposition time results in a reduced content of Ce(OH)3 in the layers, hence in an evolution of the colour of the deposits. Similarly, the increase of the temperature of the bath brings about significant modifications of the surface morphology, of the crystallite size and of the content of oxygen vacancies that are suspected not to confer adequate protection. In contrast, the addition of 10 g L-1 of PEG to the 0.1 M cerium nitrate solutions will be shown to inhibit the development of the carbonated green rust.

  3. Another Look at the Mechanisms of Hydride Transfer Enzymes with Quantum and Classical Transition Path Sampling.

    Science.gov (United States)

    Dzierlenga, Michael W; Antoniou, Dimitri; Schwartz, Steven D

    2015-04-01

    The mechanisms involved in enzymatic hydride transfer have been studied for years, but questions remain due, in part, to the difficulty of probing the effects of protein motion and hydrogen tunneling. In this study, we use transition path sampling (TPS) with normal mode centroid molecular dynamics (CMD) to calculate the barrier to hydride transfer in yeast alcohol dehydrogenase (YADH) and human heart lactate dehydrogenase (LDH). Calculation of the work applied to the hydride allowed for observation of the change in barrier height upon inclusion of quantum dynamics. Similar calculations were performed using deuterium as the transferring particle in order to approximate kinetic isotope effects (KIEs). The change in barrier height in YADH is indicative of a zero-point energy (ZPE) contribution and is evidence that catalysis occurs via a protein compression that mediates a near-barrierless hydride transfer. Calculation of the KIE using the difference in barrier height between the hydride and deuteride agreed well with experimental results. PMID:26262969

  4. Characteristics of hydriding and hydrogen embrittlement of the Ti-Al-Zr alloy

    International Nuclear Information System (INIS)

    The characteristics of hydriding and hydrogen embrittlement of the Ti-Al-Zr alloy were evaluated. The amount of hydrogen absorbed into the alloy at 500 deg. C was continuously monitored using a hydrogen pressure measurement. The rate of decrease in hydrogen pressure indicated a high absorption rate of hydrogen into the alloy, following a linear rate law. X-ray diffraction studies showed the formation of δ-phase titanium hydride (TiH1.97) after hydriding. At room temperature, the alloy showed much sensitivity to embrittlement in ductility by hydrogen. The δ-hydrides in the grain boundaries promoted the crack propagation in the presence of stress, leading to the cleavage failure mode. However, the tensile strengths were almost independent of the hydrogen content up to 1174 ppm. It is thus concluded that the δ-hydride acts to decrease the ductility without affecting tensile strengths

  5. Evaluation of hydride blisters in zirconium pressure tube in CANDU reactor

    International Nuclear Information System (INIS)

    When the garter springs for maintaining the gap between the pressure tube and the calandria tube are displaced in the CANDU reactor, the sagging of pressure tube results in a contact to the calandria tube. This causes a temperature difference between the inner and outer surface of the pressure tube. The hydride can be formed at the cold spot of outer surface and the volume expansion by hydride dormation causes the blistering in the zirconium alloys. An incident of pressure tube rupture due to the hydride blisters had happened in the Canadian CANDU reactor. This report describes the theoretical development and models on the formation and growth of hydride blister and some experimental results. The evaluation methodology and non-destructive testing for hydride blister in operating reactors are also described

  6. Assessing nanoparticle size effects on metal hydride thermodynamics using the Wulff construction.

    Science.gov (United States)

    Kim, Ki Chul; Dai, Bing; Karl Johnson, J; Sholl, David S

    2009-05-20

    The reaction thermodynamics of metal hydrides are crucial to the use of these materials for reversible hydrogen storage. In addition to altering the kinetics of metal hydride reactions, the use of nanoparticles can also change the overall reaction thermodynamics. We use density functional theory to predict the equilibrium crystal shapes of seven metals and their hydrides via the Wulff construction. These calculations allow the impact of nanoparticle size on the thermodynamics of hydrogen release from these metal hydrides to be predicted. Specifically, we study the temperature required for the hydride to generate a H(2) pressure of 1 bar as a function of the radius of the nanoparticle. In most, but not all, cases the hydrogen release temperature increases slightly as the particle size is reduced. PMID:19420649

  7. Assessing nanoparticle size effects on metal hydride thermodynamics using the Wulff construction

    International Nuclear Information System (INIS)

    The reaction thermodynamics of metal hydrides are crucial to the use of these materials for reversible hydrogen storage. In addition to altering the kinetics of metal hydride reactions, the use of nanoparticles can also change the overall reaction thermodynamics. We use density functional theory to predict the equilibrium crystal shapes of seven metals and their hydrides via the Wulff construction. These calculations allow the impact of nanoparticle size on the thermodynamics of hydrogen release from these metal hydrides to be predicted. Specifically, we study the temperature required for the hydride to generate a H2 pressure of 1 bar as a function of the radius of the nanoparticle. In most, but not all, cases the hydrogen release temperature increases slightly as the particle size is reduced.

  8. Strategies for the improvement of the hydrogen storage properties of metal hydride materials.

    Science.gov (United States)

    Wu, Hui

    2008-10-24

    Metal hydrides are an important family of materials that can potentially be used for safe, efficient and reversible on-board hydrogen storage. Light-weight metal hydrides in particular have attracted intense interest due to their high hydrogen density. However, most of these hydrides have rather slow absorption kinetics, relatively high thermal stability, and/or problems with the reversibility of hydrogen absorption/desorption cycling. This paper discusses a number of different approaches for the improvement of the hydrogen storage properties of these materials, with emphasis on recent research on tuning the ionic mobility in mixed hydrides. This concept opens a promising pathway to accelerate hydrogenation kinetics, reduce the activation energy for hydrogen release, and minimize deleterious possible by-products often associated with complex hydride systems. PMID:18821548

  9. Mobility and chemical bond of hydrogen in titanium and palladium hydrides

    International Nuclear Information System (INIS)

    The probabilities for π- meson capture by hydrogen are measured at 25, 155 and 200 deg C in TiHsub(1.65) hydride and at 25, -120 and -196 deg C in PdHsub(0.67) hydride. An analysis of the results obtained shows that within the accuracy of the measurements (approximately 10%) a sharp (up to 1012) change in the mobility of hydrogen in the hydrides induced by temperature changes within the ranges indicated does not noticeably affect the probabilities for π- meson capture by bound hydrogen, i.e. does not lead to appreciable changes in the Me-H bond. A comparison of the capture probabilities for palladium hydride and hydrides of neighboring transition metals shows that there are no pronounced anomalies in the Pd-H bond

  10. The effects of cerium doping on the size, morphology, and optical properties of α-hematite nanoparticles for ultraviolet filtration

    International Nuclear Information System (INIS)

    Highlights: • Possible application of cerium-doped α-hematite as ultraviolet filter. • Nanoparticles obtained through co-precipitation technique using various cerium doping levels followed by annealing. • Comprehensive materials characterisation utilizing XRD, DSC/TGA, STEM, UV–vis spectroscopy. • Increasing cerium content reduces particle sizing and alters morphology. • Solubility of cerium in hematite seen between 5 and 10% doping, 10% cerium doping greatly enhances attenuation in ultraviolet region and increases optical bandgap. - Abstract: Metal oxide nanoparticles have potential use in energy storage, electrode materials, as catalysts and in the emerging field of nanomedicine. Being able to accurately tailor the desirable properties of these nanoceramic materials, such as particle size, morphology and optical bandgap (Eg) is integral in the feasibility of their use. In this study we investigate the altering of both the structure and physical properties through the doping of hematite (α-Fe2O3) nanocrystals with cerium at a range of concentrations, synthesised using a one-pot co-precipitation method. This extremely simple synthesis followed by thermal treatment results in stable Fe2−xCexOy nanoceramics resulting from the burning of any unreacted precursors and transformation of goethite-cerium doped nanoparticle intermediate. The inclusion of Ce into the crystal lattice of these α-Fe2O3 nanoparticles causes a significantly large reduction in mean crystalline size and alteration in particle morphology with increasing cerium content. Finally we report an increase optical semiconductor bandgap, along with a substantial increase in the ultraviolet attenuation found for a 10% Ce-doping concentration which shows the potential application of cerium-doped hematite nanocrystals to be used as a pigmented ultraviolet filter for cosmetic products

  11. Hydride Ions, HCO+ and Ionizing Irradiation in Star Forming Region

    Science.gov (United States)

    Benz, Arnold O.; Bruderer, Simon; van Dishoeck, Ewine

    2016-06-01

    Hydrides are fundamental precursor molecules in cosmic chemistry and many hydride ions have become observable in high quality for the first time thanks to the Herschel Space Observatory. Ionized hydrides, such as CH+ and OH+ and also HCO+ affect the chemistry of molecules such as water. They also provide complementary information on irradiation by far UV (FUV) or X-rays and gas temperature.We explore hydrides of the most abundant heavier elements in an observational survey covering star forming regions with different mass and evolutionary state. Twelve YSOs were observed with HIFI on Herschel in 6 spectral settings providing fully velocity-resolved line profiles. The YSOs include objects of low (Class 0 and I), intermediate, and high mass, with luminosities ranging from 4 Ls to 2 105 Ls.The targeted lines of CH+, OH+, H2O+, and C+ are detected mostly in blue-shifted absorption. H3O+ and SH+ are detected in emission and only toward some high-mass objects. For the low-mass YSOs the column density ratios of CH+/OH+ can be reproduced by simple chemical models implying an FUV flux of 2 – 400 times the ISRF at the location of the molecules. In two high-mass objects, the UV flux is 20 – 200 times the ISRF derived from absorption lines, and 300 – 600 ISRF using emission lines. Upper limits for the X-ray luminosity can be derived from H3O+ observations for some low-mass objects.If the FUV flux required for low-mass objects originates at the central protostar, a substantial FUV luminosity, up to 1.5 Ls, is required. For high-mass regions, the FUV flux required to produce the observed molecular ratios is smaller than the unattenuated flux expected from the central object(s) at the Herschel beam radius. This is consistent with an FUV flux reduced by circumstellar extinction or by bloating of the protostar.The ion molecules are proposed to form in FUV irradiated cavity walls that are shocked by the disk wind. The shock region is turbulent, broadening the lines to some 1

  12. Data acquisition for delayed hydride cracking studies using DCPD technique

    International Nuclear Information System (INIS)

    Direct current potential drop (DCPD) is a commonly used technique for making measurements on crack propagation in Delayed Hydride Cracking (DHC) studies on materials. It consists of passing a highly stable current ( 5-15A) through a Compact Toughness (CT) specimen of the material subjected to a mechanical load at the requisite elevated temperature, and precisely measuring and tracking the very small voltage developed across two points of specific geometry on it. Though simple in principle, this involves measuring and extracting very small signals from inevitable large spurious signals in a harsh environment, and it requires a high quality data acquisition and analysis system to extract the required information from the experiment

  13. Equilibrium composition for the reaction of plutonium hydride with air

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    There are six independent constituents with 4 chemical elements, i.e. PuH2.7(s), PuN(s), Pu2O3(s), N2, O2 and H2, therefore , the system described involves of 2 independent reactions ,both those of the experimental, which indicates that the chemical equilibrium is nearly completely approached. Therefore, it is believed that the reaction rate of plutonium hydride with air is extremely rapid. The present paper has briefly discussed the simultaneous reactions and its thermodynamic coupling effect.

  14. Simulation of metal hydride reactor with aluminium foam matrix

    International Nuclear Information System (INIS)

    'Full text:' A 1-D model has been developed for testing different designs of hydride reactors. The computer program can simulate a complete reactor or a part of it in planar, cylindrical or spherical geometry. It reproduces an experimental loop: absorption followed by desorption and calculates heat transfer during the reaction. Simulation results have been confronted to experimental data with very good correlation. A reactor with a heat transfer matrix inside, such as aluminum foam, can be simulated. We have evaluated the size limits of a reactor and the category of foam that preserves the good reaction kinetic performances of a reactor filled with LaNi5. (author)

  15. Uranium-zirconium hydride TRIGA-LEU fuel

    International Nuclear Information System (INIS)

    The development and testing of TRIGA-LEU fuel with up to 45 wt-% U is described. Topics that are discussed include properties of hydride fuels, the prompt negative temperature coefficient, pulse heating tests, fission product retention, and the limiting design basis parameter and values. General specifications for Er-U-ZrH TRIGA-LEU fuel with 8.5 to 45 wt-% U and an outline of the inspections during manufacture of the fuel are also included. (author). 8 figs, 1 tab

  16. Comparison between different reactions of group IV hydride with H

    Institute of Scientific and Technical Information of China (English)

    ZHANG; Shaolong; ZHANG; Xuqiang; ZHANG; Qinggang; ZHANG; Yici

    2006-01-01

    The four-dimensional time-dependent quantum dynamics calculations for reactions of group IV hydride with H are carried out by employing the semirigid vibrating rotor target model and the time-dependent wave packet method. The reaction possibility, cross section and rate constants for reactions (H+SiH4 and H+GeH4) in different initial vibrational and rotational states are obtained. The common feature for such kind of reaction process is summarized. The theoretical result is consistent with available measurement, which indicates the credibility of this theory and the potential energy surface.

  17. A compact hydrogen recycling system using metal hydrides

    International Nuclear Information System (INIS)

    A gas recycling system to prevent losses of isotopically enriched hydrogen gas has been developed for the operation of a liquid target (2.7 l) used by the Radiative Muon Capture group at TRIUMF. The experimental requirements for high gas purity (chemical impurities below 10-9), low operating pressure (below 1 bar abs) and high loading pressure (about 10 bar needed for a palladium purifier) together with the usual hydrogen safety requirements were satisfied with a metal hydride storage device in combination with a small pump/compressor system. A description of the complete system together with its characteristic operational data are given in this paper. ((orig.))

  18. The calculated rovibronic spectrum of scandium hydride, ScH

    CERN Document Server

    Lodi, Lorenzo; Tennyson\\, Jonathan

    2015-01-01

    The electronic structure of six low-lying electronic states of scandium hydride, $X\\,{}^{1}\\Sigma^+$, $a\\,{}^{3}\\Delta$, $b\\,{}^{3}\\Pi$, $A\\,{}^{1}\\Delta$ $c\\,{}^{3}\\Sigma^+$, and $B\\,{}^{1}\\Pi$, is studied using multi-reference configuration interaction as a function of bond length. Diagonal and off-diagonal dipole moment, spin-orbit coupling and electronic angular momentum curves are also computed. The results are benchmarked against experimental measurements and calculations on atomic scandium. The resulting curves are used to compute a line list of molecular ro-vibronic transitions for $^{45}$ScH.

  19. Evolution of the local environment of cerium and neodymium during simplified SON68 glass alteration

    Energy Technology Data Exchange (ETDEWEB)

    Jollivet, Patrick [Commissariat a l' Energie Atomique (CEA), Rhone Valley Research Center, BP 17171, 30207 Bagnols-sur-Ceze (France)]. E-mail: patrick.jollivet@cea.fr; Lopez, Christophe [Commissariat a l' Energie Atomique (CEA), Rhone Valley Research Center, BP 17171, 30207 Bagnols-sur-Ceze (France); Auwer, Christophe Den [Commissariat a l' Energie Atomique (CEA), Rhone Valley Research Center, BP 17171, 30207 Bagnols-sur-Ceze (France); Simoni, Eric [Institut de Physique Nucleaire, Batiment 100, 91406 Orsay cedex (France)

    2005-11-15

    The evolution of the sites occupied by cerium and neodymium (coordination numbers and Ce, Nd-O distances) during alteration of simplified SON68 glass specimens was determined by L{sub III}-edge XAS. Cerium and neodymium are situated in a silicate environment in the glass, surrounded by eight oxygen atoms at an average distance of 2.44 and 2.48 A, respectively. These two rare earth elements exhibit different leaching behavior, however. The main environment of cerium becomes a silicate (d {sub Ce-O} = 2.19 A) with a second oxide or more probably oxyhydroxide site (d {sub Ce-O} = 2.32 A). The cerium coordination number increases by 1 to 3 compared with the glass, depending on the leaching conditions. Neodymium is found mainly in a hydroxycarbonate environment (d {sub Nd-O} = 2.46 A); the second site is a silicate (d {sub Nd-O} = 2.54 A). The neodymium coordination number increases by 1 compared with the glass. When glass containing neodymium is doped with phosphorus, Nd is situated in a phosphate environment; this change is also reflected in the coordination number and Nd-O distance (seven oxygen atoms at 2.42 A). During glass leaching, neodymium is present at two different sites, phosphate (d {sub Nd-O} = 2.52 A) and hydroxycarbonate (d {sub Nd-O} = 2.40 A)

  20. XPS and factor analysis study of initial stages of cerium oxide growth on polycrystalline tungsten

    Czech Academy of Sciences Publication Activity Database

    Polyak, Yaroslav; Bastl, Zdeněk

    2015-01-01

    Roč. 47, č. 6 (2015), s. 663-671. ISSN 0142-2421 Institutional support: RVO:68378271 ; RVO:61388955 Keywords : XPS * FA * PLD * cerium oxide * WO 3 * Ce (3d) Subject RIV: BM - Solid Matter Physics ; Magnetism; CF - Physical ; Theoretical Chemistry (UFCH-W) Impact factor: 1.245, year: 2014