WorldWideScience

Sample records for cerium compounds

  1. 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)

  2. 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

  3. 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

  4. 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

  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. 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

  7. 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.

  8. 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)

  9. Effect of Pressure on the Ferromagnetic Cerium Compound CeCu9Sn4

    International Nuclear Information System (INIS)

    Electrical resistivity measurements under hydrostatic pressure up to 2.2 GPa was carried out for a ferromagnetic ternary cerium compound CeCu9Sn4. The ferromagnetic transition temperature increases with increasing pressure up to 0.8 GPa and then decreases with increasing pressure above 1 GPa. Origins of this pressure dependence may be the competition between magnetic interaction in the c-plane and along the c-direction. (author)

  10. Influence of stoichiometry on electrochromic cerium-titanium oxide compounds

    International Nuclear Information System (INIS)

    CeO2-TiO2 finds use as passive counter-electrode in electrochromic devices. Thin films were produced by de-sputtering in a wide range of compositions. Influence of total pressure and oxygen partial pressure on the optical constants of TiO2 was investigated. Slightly substoichiometric Ti02 films exhibit a red-shift of the bandgap. The Ti02 content in the compound essentially determines the degree of cathodical coloring upon Li+ intercalation [1]. However, pure TiO2 films with comparable visible transmittance in the clear state behave differently during electrochemical cycling depending on oxygen stoichiometry. Films that are deposited at higher total pressure are more oxygen rich and require initial formatting until current voltage cycles become stable. CeO2-Ti02 films of intermediate compositions have the relatively highest charge capacity. Comparison with atomic force microscopy indicates a correlation of small grain size with high charge capacity

  11. De Haas--Van Alphen Experiments in the Quantum Critical Region of Cerium and Uranium Compounds

    International Nuclear Information System (INIS)

    When pressure is applied to the cerium and uranium compounds, their magnetic ordering temperatures are suppressed and become zero at a critical pressure Pc. Around Pc, non-Fermi liquid and/or superconductivity are observed. We clarified a change of the electronic state via the de Haas--van Alphen (dHvA) experiment when pressure crosses Pc. The dHvA experiment under pressure was done for antiferromagnets CeRh2Si2, CeRhIn5 and URu2Si2, and a ferromagnet UGe2. We find an abrupt change of the Fermi surface for CeRh2Si2 and UGe2 when crossing Pc, indicating a first-order like phase transition. For CeRhIn5 and URu2Si2, a change of the cyclotron mass is clearly observed. (author)

  12. Optical Evidence of Itinerant-Localized Crossover of 4f Electrons in Cerium Compounds

    Science.gov (United States)

    Kimura, Shin-ichi; Kwon, Yong Seung; Matsumoto, Yuji; Aoki, Haruyoshi; Sakai, Osamu

    2016-08-01

    Cerium (Ce)-based heavy-fermion materials have a characteristic double-peak structure (mid-IR peak) in the optical conductivity [σ(ω)] spectra originating from the strong conduction (c)-f electron hybridization. To clarify the behavior of the mid-IR peak at a low c-f hybridization strength, we compared the σ(ω) spectra of the isostructural antiferromagnetic and heavy-fermion Ce compounds with the calculated unoccupied density of states and the spectra obtained from the impurity Anderson model. With decreasing c-f hybridization intensity, the mid-IR peak shifts to the low-energy side owing to the renormalization of the unoccupied 4f state, but suddenly shifts to the high-energy side owing to the f-f on-site Coulomb interaction at a slight localized side from the quantum critical point (QCP). This finding gives us information on the change in the electronic structure across QCP.

  13. 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

  14. Intermetallic cerium compounds with ordered U{sub 3}Si{sub 2} type structure

    Energy Technology Data Exchange (ETDEWEB)

    Poettgen, R.; Fugmann, A.; Hoffmann, R.-D.; Rodewald, U.C.; Niepmann, D. [Muenster Univ. (Germany). Anorganisch-Chemisches Inst.

    2000-02-01

    New intermetallic cerium compounds Ce{sub 2}T{sub 2}Mg (T = Ni, Cu, Pd), Ce{sub 2}T{sub 2}Cd (T = Pd, Pt, Au), and Ce{sub 2}T{sub 2}Pb (T = Pt, Au) were prepared by reaction of the elements in sealed tantalum tubes in a high-frequency furnace. Most Ce{sub 2}T{sub 2}X (X = Mg, Cd, Pb) compounds are stable after annealing at about 1000 K, while Ce{sub 2}Pd{sub 2}Mg is obtained as single phase only after melting and quenching. A thermal treatment at about 1000 K leads to decomposition in CePdMg and CePd. The eight compounds were investigated by X-ray diffraction both as powders and single crystals, and most structures were refined from single crystal data. They adopt an ordered U{sub 3}Si{sub 2} type structure with space group P4/mbm: a = 759.6(1), c = 376.71(9) pm, wR2 = 0.0562, 294 F{sup 2} values, 12 parameters for Ce{sub 2}Ni{sub 2}Mg, a = 787.41(9), c = 387.23(7) pm, wR2 = 0.0438, 222 F{sup 2} values, 12 parameters for Ce{sub 2}Cu{sub 2}Mg, a = 777.14(8), c = 400.03(7) pm, wR2 = 0.0276, 221 F{sup 2} values, 13 parameters for Ce{sub 2}Pd{sub 2.03}Mg{sub 0.97}, a = 777.90(6), c = 393.28(6) pm, wR2 = 0.0360, 317 F{sup 2} values, 12 parameters for Ce{sub 2}Pd{sub 2}Cd, and a = 779.90(7), c = 389.97(7) pm, wR2 = 0.0453, 315 F{sup 2} values, 12 parameters for Ce{sub 2}Pt{sub 2}Cd. Refinement of the occupancy parameters revealed full occupancy for most sites. A mixed palladium/magnesium (97% Mg / 3% Pd) occupancy was observed only for the 2a site of Ce{sub 2}Pd{sub 2.03}Mg{sub 0.97}, indicating a small homogeneity range for this compound. Ce{sub 2}Au{sub 2}Cd (a = 804.93(7), c = 393.36(6) pm) and the plumbides Ce{sub 2}Pt{sub 2}Pb (a = 794.63(7), c = 381.50(6) pm) and Ce{sub 2}Au{sub 2}Pb (a = 810.70(7), c = 394.85(7) pm) were characterized through their Guinier powder data. The structures of the Ce{sub 2}T{sub 2}X compounds can be interpreted as an intergrowth of distorted AlB{sub 2} and CsCl related slabs of compositions CeT{sub 2} and CeX. The course of the lattice

  15. Influence of ethanol on catalytic properties of vanadium (5) compounds in the reaction of hydrazine oxidation by cerium (4) sulfate

    International Nuclear Information System (INIS)

    A study was made of the effect of ethyl alcohol on the rate of oxidation of hydrazine by cerium sulphate in the presence and in the absence of vanadium compounds. The addition of ethyl alcohol accelerates the oxidation reaction. In the absence of the vanadium compounds acting as catalyst, the increase in the reaction rate is due to the formation of an intermediate complex between the oxidizing agent and the ethyl alcohol. The equilibrium constant for the reaction forming the intermediate complex with composition 1:1 is 0.70+-0.05, while the constant for the rate of decomposition of the intermediate product is 0.24 min-1. In the presence of the vanadium compounds an intermediate complex is formed between the catalyst and the ethyl alcohol. The equilibrium constant for the reaction forming this complex is 0.41+-0.03, and the constant for the rate of decomposition thereof is 0.44x105min-1. (author)

  16. Mixed valency and site-preference chemistry for cerium and its compounds: A predictive density-functional theory study

    Science.gov (United States)

    Alam, Aftab; Johnson, D. D.

    2014-06-01

    Cerium and its technologically relevant compounds are examples of anomalous mixed valency, originating from two competing oxidation states—itinerant Ce4+ and localized Ce3+. Under applied stress, anomalous transitions are observed but not well understood. Here we treat mixed valency as an "alloy" problem involving two valences with competing and numerous site-occupancy configurations. We use density-functional theory with Hubbard U (i.e., DFT+U) to evaluate the effective valence and predict properties, including controlling the valence by pseudoternary alloying. For Ce and its compounds, such as (Ce,La)2(Fe,Co)14B permanent magnets, we find a stable mixed-valent α state near the spectroscopic value of νs=3.53. Ce valency in compounds depends on its steric volume and local chemistry. For La doping, Ce valency shifts towards γ-like Ce3+, as expected from steric volume; for Co doping, valency depends on local Ce-site chemistry and steric volume. Our approach captures the key origins of anomalous valency and site-preference chemistry in complex compounds.

  17. Sonochemical synthesis of a new nano-sized cerium(III) supramolecular compound; Precursor for nanoceria.

    Science.gov (United States)

    Gohari Derakhshandeh, Parviz; Soleimannejad, Janet

    2016-07-01

    Using a sonochemical method, nanoparticles of a new Ce(III) supramolecular compound, (NAMH(+))2[Ce4(pydc)6(pydcH)2(H2O)8]·8H2O (1), (H2pydc=2,6-pyridinedicarboxylic acid, NAM=nicotinamide), have been synthesized. Compound 1 was characterized by scanning electron microscopy (SEM), X-ray powder diffraction (XRPD), FT-IR spectroscopy and elemental analyses, and its structure was determined by X-ray crystallography. It has been revealed that its structure consists of tetra-nuclear building units that extend to a 3D supramolecular network via non-covalent interactions mainly hydrogen bonding. The thermal stability of complex 1 both for its crystals and nanostructures has been studied by the thermal gravimetric (TG) method and compared with each other. The role of ultrasound irradiation power and the concentration of initial reactants on the size and morphology of the nano-structured complex 1, has been investigated. Ceria nanoparticles were obtained upon the calcination of complex 1 at 800°C under atmospheric air. Furthermore, the fluorescent properties of complex 1 at room temperature were studied. PMID:26964931

  18. Selective side-chain oxidation of alkyl aromatic compounds catalyzed by cerium modified silver catalysts

    DEFF Research Database (Denmark)

    Beier, Matthias Josef; Schimmoeller, Bjoern; Hansen, Thomas Willum; Andersen, Jens Enevold Thaulov; Pratsinis, Sotiris E.; Grunwaldt, Jan-Dierk

    2010-01-01

    Silver supported on silica effectively catalyzes the aerobic side-chain oxidation of alkyl aromatic compounds under solvent-free conditions. Toluene, p-xylene, ethylbenzene and cumene were investigated as model substrates. Typically, the reaction was performed at ambient pressure; only for toluene...... an elevated pressure was required. Carboxylic acids, such as benzoic acid or p-toluic acid, additionally increased the reaction rate while CeO2 could act both as a promoter and an inhibitor depending on the substrate and the reaction conditions. Silver catalysts were prepared both by standard...... catalysis. In addition, flame-made catalysts were more stable against silver leaching compared to the impregnated catalysts. The structure of the silver catalysts was studied in detail both by X-ray absorption spectroscopy and transmission electron microscopy suggesting metallic silver to be required for...

  19. Thermal properties of some cerium compounds, particularly CeB6

    International Nuclear Information System (INIS)

    Using measurements of specific heat between 0.3 to 250K in the absence of a magnetic field, and from 2 to 250K for magnetic fields between 0 and 8T, it is shown that the γ 8 quadruplet is the fundamental level of the Ce3+ ion, the γ 8-7 separation energy being of the order of 500K. Detailed analysis suggests a lifting of degeneracy of the multiplet γ 8 in the paramagnetic phase, according to usual processes. Specific heat results obtained at very low temperatures reveal the importance of a significant gap in the spin wave energy spectra. Measurements under a strong magnetic field, around the two magnetic phase transitions of CeB6 show a spectacular reinforcement of the specific heat anomaly at a temperature of the order of TQ. Thermal conductivity of CEB6 is also studied in relation to the possible existence of a Jahn-Teller effect, likely to affect heat transfer by phonons. The problem of the different components of thermal transport prompts the analysis of the Weidemann-Franz law in the Kondo net, and also the study of the thermal conductivity of the compounds CeCu6, CeA12, the alloys Ce0.75La0.25B6, CexLa1-xCu6, and the fluctuating valence system SmB6. In all these bodies, an important contribution of phonons to electron transfer is shown. In the dense incoherent Kondo phase, it is not possible to envisage differences from the Weidemann-Franz law greater than those observed for highly diluted Kondo alloys

  20. 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

  1. 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.)

  2. The cerium ground state in the intermetallic compounds Al2Ce, Al3Ce at very low temperature

    International Nuclear Information System (INIS)

    Nuclear orientation experiments show the different behaviour between the Al2Ce and Al3Ce compounds. Despite the occurrence of a Kondo coupling, the first compound is well ordered down to 5 mK. No long range ordering seems to exist in Al3Ce but crystal field effects can partly mask the ordering. (author)

  3. Improvements in or relating to compounds

    International Nuclear Information System (INIS)

    The invention provides a process for the preparation of a dispersible product containing a cerium compound which comprises heating a cerium (IV) oxide hydrate in the presence of a salt to cause deaggregation of aggregated crystallites in the cerium (IV) oxide hydrate and produce a dispersible product containing a cerium compound. (author)

  4. 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.

  5. 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.

  6. 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

  7. Coexistence of antiferromagnetism and superconductivity in heavy fermion cerium compound Ce.sub.3./sub.PdIn.sub.11./sub

    Czech Academy of Sciences Publication Activity Database

    Kratochvílová, M.; Prokleška, J.; Uhlířová, K.; Tkáč, V.; Dušek, Michal; Sechovský, V.; Custers, J.

    2015-01-01

    Roč. 5, Oct (2015), s. 15904. ISSN 2045-2322 R&D Projects: GA ČR(CZ) GAP204/11/0809 Institutional support: RVO:68378271 Keywords : crystal structure * magnetic transition * heavy fermion compounds * antiferromagnetism Subject RIV: BM - Solid Matter Physics ; Magnetism Impact factor: 5.578, year: 2014

  8. 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

  9. 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

  10. 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.

  11. 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.

  12. 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.

  13. 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.

  14. Influence of interstitial solutions (H, N) on cerium electronic state in Ce-Fe intermetallic compounds: X-ray Absorption Spectroscopy (XAS) study

    International Nuclear Information System (INIS)

    It is presented an x-ray absorption spectroscopy (XAS) investigation performed at the L-edges of the rare-earth and at the K-edge of iron in the R-Fe intermetallic compounds (La, Ce)2Fe14BHχand Ce2Fe17(H,N)χ, to elucidate the role of the interstitial doping into the electronic and magnetic properties of these systems. Comparison with x-ray circular magnetic dichroism (XCMD) experiments has been carried out to clarify the localization of 4f magnetic moment at the Ce sites upon hydriding. Both XAS and XCMD results evidence the interplay between the structural and magnetic changes, that are associated to the modification of the hybridization between the Fe(3d) and Ce(5d) bands

  15. 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

  16. Thermal, Mechanical and UV-Shielding Properties of Poly(Methyl Methacrylate/Cerium Dioxide Hybrid Systems Obtained by Melt Compounding

    Directory of Open Access Journals (Sweden)

    María A. Reyes-Acosta

    2015-09-01

    Full Text Available Thick and homogeneous hybrid film systems based on poly(methyl methacrylate (PMMA and CeO2 nanoparticles were synthesized using the melt compounding method to improve thermal stability, mechanical and UV-shielding properties, as well as to propose them for use in the multifunctional materials industry. The effect of the inorganic phase on these properties was assessed by using two different weight percentages of synthesized CeO2 nanoparticles (0.5 and 1.0 wt % with the sol–gel method and thermal treatment at different temperatures (120, 235, 400, 600 and 800 °C. Thereafter, the nanoceria powders were added to the polymer matrix by single screw extrusion. The absorption in the UV region was increased with the crystallite size of the CeO2 nanoparticles and the PMMA/CeO2 weight ratio. Due to the crystallinity of CeO2 nanoparticles, the thermal, mechanical and UV-shielding properties of the PMMA matrix were improved. The presence of CeO2 nanostructures exerts an influence on the mobility of PMMA chain segments, leading to a different glass transition temperature.

  17. Analysis of single and binary phases in cerium doped sodium bismuth titanate -inorganic materials Na0.5Bi(0.5-x)CexTiO3

    International Nuclear Information System (INIS)

    The pure and cerium doped sodium bismuth titanate (NBT) inorganic powders were synthesized by solid-state reaction method. The presence of rhombohedral phase was observed in cerium doped NBT compounds. When x= 0.05 of cerium doped NBT is heat treated at 1200 degree centigrade, the compound forms single perovskite phase. The samples of x = 0.10 and 0.15 were heat treated up to 1350 degree centigrade, the binary phases with cerium and bismuth oxides were observed. The X-ray diffraction, Fourier transform infrared spectroscopy, reflectance spectra, differential thermal analysis and thermogravimetric analysis were used to analyze the various properties of samples. Moreover, the effects of cerium doping and calcining temperature on NBT samples were investigated. In this work, we present our recent results on the synthesis and characterization of cerium doped sodium bismuth titanate materials. (Author)

  18. 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.

  19. 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.

  20. 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.

  1. 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...

  2. 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].

  3. 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].

  4. 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.

  5. 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)

  6. 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.

  7. 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.

  8. 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.

  9. 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.

  10. 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

  11. 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...

  12. 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

  13. 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.

  14. 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

  15. 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

  16. 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

  17. 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...

  18. 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

  19. 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.

  20. 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

  1. 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.

  2. 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

  3. A Novel Open-Framework Cerium Phosphate Fluoride: (NH 4)[Ce IVF 2(PO 4)

    Science.gov (United States)

    Yu, Ranbo; Wang, Dan; Takei, Takahiro; Koizumi, Hitoshi; Kumada, Nobuhiro; Kinomura, Nobukazu

    2001-02-01

    A novel open-framework cerium phosphate fluoride, (NH4)[CeIVF2(PO4)], has been synthesized under hydrothermal conditions and characterized by means of single-crystal X-ray diffraction, ion chromatography analysis, and thermal analysis. The compound crystallizes in the monoclinic space group P21/m(No. 11), with a=6.660(2), b=5.875(2), c=7.177(3) Å, β=114.31(2)°, and V=255.9(2) Å3 (R=0.039 and Rw=0.045). In this compound, the cerium-centered CeO4F4 polyhedra link via Ce2F2 rings to form corrugated chains along the b axis of the structure. These are tetrahedrally connected via PO4 groups to create the three-dimensional network with a one-dimensional channel. NH+4 cations are accommodated at the intersection of the channels.

  4. 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

  5. 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

  6. Analysis of single and binary phases in cerium doped sodium bismuth titanate -inorganic materials Na{sub 0}.5Bi{sub (}0.5-x)Ce{sub x}TiO{sub 3}; Estudio de fases simples y binarias en BNT puro y dopado con cerio Na{sub 0},5Bi{sub (}0,5-x)Ce{sub x}TiO{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Supriya, S.; Dos Santos-Garcia, A. J.; Frutos, J. de; Fernandez-Martinez, F.

    2015-07-01

    The pure and cerium doped sodium bismuth titanate (NBT) inorganic powders were synthesized by solid-state reaction method. The presence of rhombohedral phase was observed in cerium doped NBT compounds. When x= 0.05 of cerium doped NBT is heat treated at 1200 degree centigrade, the compound forms single perovskite phase. The samples of x = 0.10 and 0.15 were heat treated up to 1350 degree centigrade, the binary phases with cerium and bismuth oxides were observed. The X-ray diffraction, Fourier transform infrared spectroscopy, reflectance spectra, differential thermal analysis and thermogravimetric analysis were used to analyze the various properties of samples. Moreover, the effects of cerium doping and calcining temperature on NBT samples were investigated. In this work, we present our recent results on the synthesis and characterization of cerium doped sodium bismuth titanate materials. (Author)

  7. 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

  8. 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)

  9. 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.

  10. 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.

  11. 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

  12. 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.

  13. 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.)

  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. Cerium valence change in the solid solutions Ce(Rh1-xRux)Sn

    International Nuclear Information System (INIS)

    The solid solutions Ce(Rh1-xRux)Sn were investigated by means of susceptibility measurements, specific heat, electrical resistivity, X-ray absorption spectroscopy (XAS), and 119Sn Moessbauer spectroscopy. Magnetic measurements as well as XAS data show a cerium valence change in dependence on the ruthenium content. Higher ruthenium content causes an increase from 3.22 to 3.45 at 300 K. Furthermore χ and χ-1 data indicate valence fluctuation for cerium as a function of temperature. For example, Ce(Rh0.8Ru0.2)Sn exhibits valence fluctuations between 3.42 and 3.32 in the temperature range of 10 to 300 K. This could be proven by using the interconfiguration fluctuation (ICF) model introduced by Sales and Wohlleben. Cerium valence change does not influence the tin atoms as proven by 119Sn Moessbauer spectroscopy, but it influences the electrical properties. Ce(Rh0.9Ru0.1)Sn behaves like a typical valence fluctuating compound, and higher ruthenium content causes an increase of the metallic behavior. (orig.)

  17. Effect of coating parameters on the microstructure of cerium oxide conversion coatings

    International Nuclear Information System (INIS)

    The microstructure and morphology of cerium oxide conversion coatings prepared under different deposition conditions were characterized by transmission electron microscopy (TEM). The coatings were formed by a spontaneous reaction between a water-based solution containing CeCl3 and aluminum alloy 7075-T6 substrates. Microstructural characterization was performed to determine the crystallinity of the coatings and to obtain a better understanding of the deposition parameters on coating microstructure. The results of TEM imaging and electron diffraction analysis indicated that the as-deposited coating was composed of nanocrystalline particles of a previously unreported cerium compound. The particles of the coatings produced using glycerol as an additive were found to be much finer than those of the coatings prepared in the absence of glycerol. This indicates that glycerol may act as a grain refiner and/or growth inhibitor during coating deposition. After deposition, the coated panels were treated for 5 min in a phosphate sealing solution. The sealing treatment converted the as-deposited coating into hydrated cerium phosphate. Panels coated from solutions containing no glycerol followed by phosphate sealing performed poorly in salt fog tests. With glycerol addition, the corrosion resistance of the coatings that were phosphate sealed improved considerably, achieving an average passing rate of 85%

  18. 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.

  19. Investigations on Ce- and Yb-based intermetallic compounds

    International Nuclear Information System (INIS)

    The author describes investigations on a number of cerium- and ytterbium-based intermetallic compounds and alloys, yielding a lot of experimental results which could not always be put in a quantitative picture. All experimental data are consistent with a single-ion behaviour, where the 4f state is more or less modified by the conduction electrons. In the investigated systems several different features of the magnetism of cerium atoms in metals were studied. (Auth.)

  20. 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

  1. 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...

  2. 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

  3. 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.

  4. 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

  5. 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

  6. Recovery of Cerium Dioxide from Spent Glass-Polishing Slurry and Its Utilization as a Reactive Sorbent for Fast Degradation of Toxic Organophosphates

    Directory of Open Access Journals (Sweden)

    Pavel Janoš

    2015-01-01

    Full Text Available The recovery of cerium (and possibly other rare earth elements from the spent glass-polishing slurries is rather difficult because of a high resistance of polishing-grade cerium oxide toward common digestion agents. It was shown that cerium may be extracted from the spent polishing slurries by leaching with strong mineral acids in the presence of reducing agents; the solution may be used directly for the preparation of a ceria-based reactive sorbent. A mixture of concentrated nitric acid and hydrogen peroxide was effective in the digestion of partially dewatered glass-polishing slurry. After the removal of undissolved particles, cerous carbonate was precipitated by gaseous NH3 and CO2. Cerium oxide was prepared by a thermal decomposition of the carbonate precursor in an open crucible and tested as reactive sorbent for the degradation of highly toxic organophosphate compounds. The samples annealed at the optimal temperature of approximately 400°C exhibited a good degradation efficiency toward the organophosphate pesticide fenchlorphos and the nerve agents soman and VX. The extraction/precipitation procedure recovers approximately 70% of cerium oxide from the spent polishing slurry. The presence of minor amounts of lanthanum does not disturb the degradation efficiency.

  7. 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

  8. 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.

  9. 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+

  10. 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.)

  11. 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...

  12. 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

  13. 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.)

  14. 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.)

  15. 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.

  16. New insights on the thermal decomposition of lanthanide(III) and actinide(III) oxalates: from neodymium and cerium to plutonium

    OpenAIRE

    De Almeida, Lucie; Grandjean, Stéphane; Vigier, Nicolas; Patisson, Fabrice

    2012-01-01

    Lanthanides are often used as surrogates to study the properties of actinide compounds. Their behaviour is considered to be quite similar as they both possess f valence electrons and are close in size and chemical properties. This study examines the potential of using two lanthanides (neodymium and cerium) as surrogates for plutonium during the thermal decomposition of isomorphic oxalate compounds, in the trivalent oxidation state, into oxides. Thus, the thermal decomposition of neodymium, ce...

  17. 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

  18. Ternary Plutonium-Cerium-Nickel Alloys as a Possible Fuel for Fast Reactors with Liquid Metal Cores

    International Nuclear Information System (INIS)

    The authors present results of a study of ternary plutonium-cerium-nickel alloys. From metallographic. thermal and X-ray analyses of these ternary alloys they obtained the projection of the liquidus curve onto the concentration triangle and the contours of the phase regions of the phase diagram over the isothermal cross-section for 400°C. The existence is established of a continuous series of solid solutions between the intermetallic compounds CeNi and PuNi, The maximum solubility of plutonium in the compound Ce7Ni3 is approximately 47.0 at. %. In the plutonium-cerium-nickel system there is a ternary eutectic with its melting point at 480°C. The composition of this eutectic is as follows: 45 at. % plutonium, 30 at. % cerium and 25 at.% nickel. The authors assume the existence of a peritectic point, the composition of which is not accurately established. The alloys, which lie along the valley line connecting the binary eutectics in the CeNi, PuNi system have a melting point not higher than 470°C. These alloys have a promising future as a fuel for fast reactors with liquid metal cores. (author)

  19. Mechanism of trace cerium in ultra-clean IF steel%微量稀土铈在超洁净IF钢中的作用

    Institute of Scientific and Technical Information of China (English)

    杨吉春; 栗宏伟; 周莉; 张剑; 刘南

    2015-01-01

    The existence forms of cerium in ultra-IF steel,in which the contents of oxygen and sulphur were both less than 0.000 6%,were studied by chemical analysis,thermodynamic calculation,micro-examination and hardness mea-surement. And the effects of cerium on Al2O3 inclusions,microstructure and hardness were discussed. The results show that,when the cerium content was between 0.006 1%and 0.009 3%,the solid solubility of cerium range from 0.004 1%to 0.006 7%. About seventy percent of cerium is in the form of solid solution,the rest of cerium is in the form of inclu-sions,and there is no Ce-Fe intermetallic compound in the steel. By adding cerium,Al2O3 inclusions are modified into smaller globular CeAlO3 inclusions. Cerium played a role in modifying inclusions in the steel. Cerium has the effect of re-fining the microstructures of the steel. The greater the amount of solid solution of cerium was,the finer the crystalline grains were. When the content of cerium are 0.006 1%and 0.009 3%,Rockwell hardness increases by 7.6%and 12.7%re-spectively compared with IF steel without cerium.%采用化学成分分析、热力学计算、显微观察、硬度测定的方法,研究了稀土铈在氧和硫质量分数均小于0.0006%的超洁净IF钢中的存在状态,以及铈对钢的Al2O3夹杂物、显微组织和硬度的影响机理。结果表明,当铈质量分数为0.0061%~0.0093%时,铈的固溶量为0.0041%~0.0067%,约70%的铈以固溶形态存在,其余的铈以夹杂物形态存在,钢中不存在铈铁金属间化合物。铈能够将Al2O3夹杂物转化为尺寸较小的球状CeAlO3夹杂物,具有变质夹杂物的作用。铈具有改善IF钢的显微组织的作用,钢中铈的固溶量越大,晶粒越细。与不含铈的IF钢相比,当钢中铈质量分数为0.0061%和0.0093%时,钢的洛氏硬度分别提高了7.6%和12.7%。

  20. Steric and electronic effects of 1,3-disubstituted cyclopentadienyl ligands on metallocene derivatives of Cerium, Titanium, Manganese, and Iron

    Energy Technology Data Exchange (ETDEWEB)

    Sofield, C.D.

    2000-05-19

    Sterically demanding 1,3-disubstituted cyclopentadienyl ligands were used to modify the physical properties of the corresponding metallocenes. Sterically demanding ligands provided kinetic stabilization for trivalent cerium compounds. Tris(di-t-butylcyclopentadienyl)cerium was prepared and anion competition between halides and cyclopentadienyl groups which had complicated synthesis of the tris(cyclopentadienyl)compound was qualitatively examined. Bis(di-t-butylcyclopentadienyl)cerium methyl was prepared and its rate of decomposition, by ligand redistribution, to tris(di-t-butylcyclopentadienyl)cerium was shown to be slower than the corresponding rate for less sterically demanding ligands. Asymmetrically substituted ligands provided a symmetry label for examination of chemical exchange processes. Tris[trimethylsilyl(t-butyl)cyclopentadienyl]cerium was prepared and the rate of interconversion between the C1 and C3 isomers was examined. The enthalpy difference between the two distereomers is 7.0 kJ/mol. The sterically demanding cyclopentadienyl ligands ansa-di-t-butylcyclopentadiene (Me2Si[(Me3C)2C5H3]2), ansa-bis(trimethylsilyl)cyclopentadiene (Me2Si[(Me3Si)2C5H3]2) and tetra-t-butylfulvalene and metallocene derivatives of the ligands were prepared and their structures were examined by single crystal X-ray crystallography. The effect that substituents on the cyclopentadienyl ring have on the pi-electron system of the ligand was examined through interaction between ligand and metal orbitals. A series of 1,3-disubstituted manganocenes was prepared and their electronic states were determined by solid-state magnetic susceptibility, electron paramagnetic resonance, X-ray crystallography, and variable temperature UV-vis spectroscopy. Spin-equilibria in [(Me3C)2C5H3]2Mn and [(Me3C)(Me3Si)C5H3]2Mn were examined and indicate an enthalpy difference of 15 kJ/mol between the high-spin and low-spin forms. Cyclopentadienyl groups resistant to intramolecular oxidative addition

  1. Many-body effects in heavy fermion compounds [sic]. Final technical report for period September 1984 - January 2001

    Energy Technology Data Exchange (ETDEWEB)

    Riseborough, Peter S.

    2002-05-01

    A theoretical investigation of many-body effects in Cerium and Uranium Heavy Fermion and Mixed Valent Compounds and their experimental manifestations in thermodynamic, transport, and spectroscopic properties is discussed in this report.

  2. The Electrodiffusion of Trace Elements in γ-Cerium, γ-Uranium and ϵ-Plutonium

    International Nuclear Information System (INIS)

    Measurements of solid state diffusion, in an electric field, of various metals in trace concentrations have been made using cerium, uranium and plutonium as solvent metals. An apparatus is described which permits sustained experiments in a controlled atmosphere under constant temperature conditions. Extensive data have been obtained in the case of cerium in the temperature range of 490 - 650°C at current densities from 250 to 500 A/cm2 and over times up to 240 hours. Data are presented for a dozen solute elements. In the case of some transition elements, notably iron, cobalt and nickel, the migration is quite rapid. The use of radioactive tracers, where possible, provided data for quantitative treatment of the results. Spectroscopic analysis provided additional information. Migration rates in uranium measured at 900°C were lower and reduced even more in plutonium at 500°C. However, it was still possible to measure a rate of electrodiffusion of iron. No movement was detected for antimony, magnesium, manganese, silicon or zirconium. With the exception of molybdenum and tin, the metals studied migrated towards the anode. Electrodiffusion presumably results from the net effect of the electric field acting on the ions and from momentum interchange between the ions and conduction electrons. The two effects may thus oppose or reinforce each other. It is felt that the field effect is greater in the cases studied. The tendency of the solute element to form a compound with the solvent metal is one measure of whether migration is to be expected. It is also shown that a relative size effect is important. An interesting aspect of the electrodiffusion of iron in cerium is the very low (∼2 kcal) activation energy. Some comparisons have been made with chemical gradient diffusion. (author)

  3. 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

  4. 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

  5. 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

  6. 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.

  7. 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.

  8. 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)

  9. 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.

  10. 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

  11. 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.

  12. 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

  13. Cerium valence change in the solid solutions Ce(Rh{sub 1-x}Ru{sub x})Sn

    Energy Technology Data Exchange (ETDEWEB)

    Niehaus, Oliver; Riecken, Jan F.; Winter, Florian; Poettgen, Rainer [Muenster Univ. (Germany). Inst. fuer Anorganische und Analytische Chemie; Muenster Univ. (Germany). NRW Graduate School of Chemistry; Abdala, Paula M. [European Synchrotron Radiation Facility (ESRF), Grenoble (France). SNBL; Chevalier, Bernard [Bordeaux Univ., Pessac (France). CNRS, ICMCB

    2013-09-15

    The solid solutions Ce(Rh{sub 1-x}Ru{sub x})Sn were investigated by means of susceptibility measurements, specific heat, electrical resistivity, X-ray absorption spectroscopy (XAS), and {sup 119}Sn Moessbauer spectroscopy. Magnetic measurements as well as XAS data show a cerium valence change in dependence on the ruthenium content. Higher ruthenium content causes an increase from 3.22 to 3.45 at 300 K. Furthermore {chi} and {chi}{sup -1} data indicate valence fluctuation for cerium as a function of temperature. For example, Ce(Rh{sub 0.8}Ru{sub 0.2})Sn exhibits valence fluctuations between 3.42 and 3.32 in the temperature range of 10 to 300 K. This could be proven by using the interconfiguration fluctuation (ICF) model introduced by Sales and Wohlleben. Cerium valence change does not influence the tin atoms as proven by {sup 119}Sn Moessbauer spectroscopy, but it influences the electrical properties. Ce(Rh{sub 0.9}Ru{sub 0.1})Sn behaves like a typical valence fluctuating compound, and higher ruthenium content causes an increase of the metallic behavior. (orig.)

  14. Cerium oxide nanoparticles coated by surfactant sodium bis(2-ethylhexyl) sulphosuccinate (AOT): local atomic structures and x-ray absorption spectroscopic studies

    International Nuclear Information System (INIS)

    Cerium oxide nanoparticles coated by sodium bis(2-ethylhexyl) sulphosuccinate (AOT) were prepared by using a microemulsion method. Transmission electron microscopy revealed an average particle size of 2-3 nm. X-ray diffraction showed that the cerium oxide nanoparticles retain the CeF2-type cubic structures like the bulk crystal. The intermediate valence of formally tetravalent compounds had been detected by x-ray-absorption near-edge structure (XANES) spectra of Ce LIII absorption in bulk CeO2 and the cerium oxide nanoparticles. Two well resolved white lines can be assigned to the electron configurations of 4f0L and 4f1L, respectively, where L denotes a ligand hole. At the same time, the cerium oxide nanoparticles also showed the structural features of trivalent compounds, in comparison to the trivalent Ce(NO3)3·6H2O. Four Lorentzian functions and two arctan functions were used to fit the normalized XANES spectra. The extended x-ray-absorption fine-structure (EXAFS) technique was used to probe the local atomic structures around the absorber Ce. The multielectron excitation effect on the EXAFS spectra was eliminated. A core-shell model was used to deduce the near-neighbour structural parameters around cerium. Bulk CeO2 with eight oxygen atoms located at 2.343 A was used as the reference sample to extract the backscattering amplitude and phase shift of the Ce-O bond. One half of the atoms locate at the core part with the CeF2-type cubic structures (eight oxygens at 2.343 A around Ce), the other half of the atoms are amorphous phase located in the shell part (surface of the nanoparticles) with approximately Ce2O3 structural features (averaged seven oxygens at 2.50 A around Ce). (author)

  15. 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.

  16. 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)

  17. 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.

  18. EMISSION REDUCTION FROM A DIESEL ENGINE FUELED BY CERIUM OXIDE NANO-ADDITIVES USING SCR WITH DIFFERENT METAL OXIDES COATED CATALYTIC CONVERTER

    Directory of Open Access Journals (Sweden)

    B. JOTHI THIRUMAL

    2015-11-01

    Full Text Available This paper reports the results of experimental investigations on the influence of the addition of cerium oxide in nanoparticle form on the major physiochemical properties and the performance of diesel. The fuel is modified by dispersing the catalytic nanoparticle by ultrasonic agitation. The physiochemical properties of sole diesel fuel and modified fuel are tested with ASTM standard procedures. The effects of the additive nanoparticles on the individual fuel properties, the engine performance, and emissions are studied, and the dosing level of the additive is optimized. Cerium oxide acts as an oxygen-donating catalyst and provides oxygen for the oxidation of CO during combustion. The active energy of cerium oxide acts to burn off carbon deposits within the engine cylinder at the wall temperature and prevents the deposition of non-polar compounds on the cylinder wall which results in reduction in HC emission by 56.5%. Furthermore, a low-cost metal oxide coated SCR (selective catalyst reduction, using urea as a reducing agent, along with different types of CC (catalytic converter, has been implemented in the exhaust pipe to reduce NOx. It was observed that a reduction in NOx emission is 50–60%. The tests revealed that cerium oxide nanoparticles can be used as an additive in diesel to improve complete combustion of the fuel and reduce the exhaust emissions significantly.

  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. 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

  2. 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

  3. 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.

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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.

  9. 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.

  10. 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

  11. 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.

  12. 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)

  13. 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

  14. 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...

  15. 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)

  16. 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)

  17. Effect of Cerium on the Viscosity of Liquid Fe-C Alloy of Eutectic Content

    Institute of Scientific and Technical Information of China (English)

    滕新营; 叶以富; 刘含莲; 王焕荣; 石志强; 耿浩然

    2002-01-01

    The viscosities of liquid Fe-4.30C and Fe-4.30C-Ce alloys were measured by oscillating crucible viscometer. The results show that viscosity of Fe-4.30C alloy changes from 5.50 to 8.30 MPa*s when the liquid is cooled from 1425 ℃ to the melting point. The abnormity of viscosity of Fe-4.30C alloy near the melting point is reasonable due to the formation of graphite. The addition of cerium especially with content higher than 0.21% causes an evidently decrease in viscosity for eutectic alloy resulting from increase of free volume and size decrease of atom cluster in the liquids. It can be concended that the existence of C-Ce compound contributes to the discontinuous of viscosity at 1340~1370 ℃ for the Fe-4.30C-Ce alloy by experinments with differential scanning calorimeter.

  18. Aqueous systems of ethanolamine hydrochlorides and of chlorides of cerium, terbium, dysprosium, erbium

    International Nuclear Information System (INIS)

    The isothermal method of cross sections has been used to study the solubility at 25 and 50 deg C in ternary water-salt systems consisting of cerium chloride and mono-(1), di-(2) and triethanolamine (3) hydrochlorides as well as diethanolamine hydrochloride and terbium, dysprosium and erbium chlorides. Solubility isotherms testify to the formation in the system (1) of a congruently dissolved compound of the CeCl3x2(C2H4OHNN2HCl)x2H2O composition. Individual peculiarities of a new solid phase are proved by the DTA method by means of derivatograph ODL-106, while the composition is confirmed by chemical analysis. The rest of the systems - are of simple eutonic type

  19. 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.

  20. High-pressure synthesis and characterization of the first cerium fluoride borate CeB2O4F

    International Nuclear Information System (INIS)

    CeB2O4F is the first cerium fluoride borate, which is exclusively built up of one-dimensional, infinite chains of condensed trigonal-planar [BO3]3− groups. This new cerium fluoride borate was synthesized under high-pressure/high-temperature conditions of 0.9 GPa and 1450 °C in a Walker-type multianvil apparatus. The compound crystallizes in the orthorhombic space group Pbca (No. 61) with eight formula units and the lattice parameters a=821.63(5), b=1257.50(9), c=726.71(6) pm, V=750.84(9) Å3, R1=0.0698, and wR2=0.0682 (all data). The structure exhibits a 9+1 coordinated cerium ion, one three-fold coordinated fluoride ion and a one-dimensional chain of [BO3]3− groups. Furthermore, IR spectroscopy, Electron Micro Probe Analysis and temperature-dependent X-ray powder diffraction measurements were performed. - Graphical abstract: A new rare-earth fluoride borate CeB2O4F could be synthesized under high-pressure/high-temperature conditions of 0.9 °GPa and 1450 °Cin a Walker-type multianvil apparatus. The crystal structure represents a new structure type in the class of rare-earth fluoride borates. The structure exhibits a 9+1 coordinated cerium ion, one three-fold coordinated fluoride ion and a one-dimensional chain of [BO3]3− groups. A closer view on the ac-plane shows an interesting wave-like modulation of the borate chains. Highlights: • CeB2O4F is the first fluoride borate exclusively built up of one-dimensional, infinite chains of condensed trigonal-planar [BO3]3− groups. • CeB2O4F is the first cerium fluoride borate. • High-pressure conditions were necessary to synthesize CeB2O4F

  1. 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)

  2. [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

  3. 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.

  4. 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

  5. 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}.

  6. 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.

  7. 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.

  8. Electrochemical extraction of cerium from CeO2 assisted by AlCl3 in molten LiCl-KCl

    International Nuclear Information System (INIS)

    This work concerns the co-reduction behaviors of Ce(III) with Al(III) ions and electrochemical extraction of cerium from cerium dioxide in molten LiCl-KCl at the temperature of 773K. Cyclic voltammetry (CV), square wave voltammetry (SWV), chronopotentiometry (CP), and open circuit chronopotentiometry (OCP) techniques were employed to investigate the electrochemical behaviors of Ce(III) and Al(III) ions on molybdenum (Mo) electrode. The results revealed Ce(III) and Al(III) cations can be co-reduced at the surface of the Mo electrode by forming different kinds of Ce-Al alloys. Finally, potentiostatic electrolysis at different deposition potentials on Al plate electrodes was also performed to prepare Ce-Al alloys. The deposition products were analyzed by X-ray diffraction (XRD) and scanning electron microscopy (SEM) with energy dispersive spectrometry (EDS). It was found that only one intermetallic compound (Al11Ce3) could be formed at the deposition potential of -1.6 V and two intermetallic compounds (Al11Ce3 and Al3Ce) could be formed at the potential of -1.9 V. When the deposition potential was negative than -2.1 V, cerium-rich alloy (AlCe) could be obtained on the surface of the Al electrode

  9. 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.

  10. Freshwater dispersion stability of PAA-stabilised cerium oxide nanoparticles and toxicity towards Pseudokirchneriella subcapitata

    International Nuclear Information System (INIS)

    An aqueous dispersion of poly (acrylic acid)-stabilised cerium oxide (CeO2) nanoparticles (PAA-CeO2) was evaluated for its stability in a range of freshwater ecotoxicity media (MHRW, TG 201 and M7), with and without natural organic matter (NOM). In a 15 day dispersion stability study, PAA-CeO2 did not undergo significant aggregation in any media type. Zeta potential varied between media types and was influenced by PAA-CeO2 concentration, but remained constant over 15 days. NOM had no influence on PAA-CeO2 aggregation or zeta potential. The ecotoxicity of the PAA-CeO2 dispersion was investigated in 72 h algal growth inhibition tests using the freshwater microalgae Pseudokirchneriella subcapitata. PAA-CeO2 EC50 values for growth inhibition (GI; 0.024 mg/L) were 2–3 orders of magnitude lower than pristine CeO2 EC50 values reported in the literature. The concentration of dissolved cerium (Ce3+/Ce4+) in PAA-CeO2 exposure suspensions was very low, ranging between 0.5 and 5.6 μg/L. Free PAA concentration in the exposure solutions (0.0096–0.0384 mg/L) was significantly lower than the EC10 growth inhibition (47.7 mg/L) value of pure PAA, indicating that free PAA did not contribute to the observed toxicity. Elemental analysis indicated that up to 38% of the total Cerium becomes directly associated with the algal cells during the 72 h exposure. TOF-SIMS analysis of algal cell wall compounds indicated three different modes of action, including a significant oxidative stress response to PAA-CeO2 exposure. In contrast to pristine CeO2 nanoparticles, which rapidly aggregate in standard ecotoxicity media, PAA-stabilised CeO2 nanoparticles remain dispersed and available to water column species. Interaction of PAA with cell wall components, which could be responsible for the observed biomarker alterations, could not be excluded. This study indicates that the increased dispersion stability of PAA-CeO2 leads to an increase in toxicity compared to pristine non-stabilised forms

  11. 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.

  12. 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.

  13. 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.

  14. 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

  15. 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

  16. 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.

  17. Structure, dielectric and electrical properties of cerium doped barium zirconium titanate ceramics

    Energy Technology Data Exchange (ETDEWEB)

    Feng Hongjun; Hou Jungang [Key Laboratory for Advanced Ceramic and Machining Technology of Ministry of Education, Tianjin University, Tianjin 300072 (China); Qu Yuanfang, E-mail: yfqu@tju.edu.cn [Key Laboratory for Advanced Ceramic and Machining Technology of Ministry of Education, Tianjin University, Tianjin 300072 (China); Shan Dan [Key Laboratory for Advanced Ceramic and Machining Technology of Ministry of Education, Tianjin University, Tianjin 300072 (China); Yao Guohua [Zhejiang Jiakang Electronics Co. Ltd., Jiaxing, Zhejiang 314000 (China)

    2012-01-25

    Highlights: Black-Right-Pointing-Pointer Rare-earth doped barium zirconate titanate (BZT) ceramics, Ba(Zr{sub 0.25}Ti{sub 0.75})O{sub 3} + xCeO{sub 2}, (x = 0-1.5 at%) were obtained by a solid state reaction route. Black-Right-Pointing-Pointer Morphological analysis on sintered samples by scanning electron microscopy shows that the addition of rare-earth ions affects the growth of the grain and remarkably changes the grain morphology. Black-Right-Pointing-Pointer The effect of rare-earth addition to BZT on dielectric and electrical properties is analyzed, demonstrating that the samples with x = 0.4 and x = 0.6 could be semiconducting in air atmosphere. - Abstract: Rare-earth doped barium zirconium titanate (BZT) ceramics, Ba(Zr{sub 0.25}Ti{sub 0.75})O{sub 3} + xCeO{sub 2}, (x = 0-1.5 at%) were obtained by a solid state reaction route. Perovskite-like single-phase compounds were confirmed from X-ray diffraction data and the lattice parameters were refined by the Rietveld method. It is found that, integrating with the lattice parameters and the distortion of crystal lattice, there is an alternation of substitution preference of cerium ions for the host cations in perovskite lattice. Morphological analysis on sintered samples by scanning electron microscopy shows that the addition of rare-earth ions affects the growth of the grain and remarkably changes the grain morphology. The effect of rare-earth addition to BZT on dielectric and electrical properties is analyzed. High values of dielectric tunability are obtained for cerium doped BZT. Especially, the experimental results on the effect of the contents of rare-earth addition on the resistivity of BZT ceramics were investigated, demonstrating that the samples with x = 0.4 and x = 0.6 could be semiconducting in air atmosphere.

  18. 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...

  19. 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

  20. 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.

  1. 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...

  2. 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

  3. 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

  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. 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

  7. 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

  8. 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.

  9. 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)

  10. 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.

  11. 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.

  12. 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

  13. Synthesis and theoretical investigations of the solid solution CeRu(1-x)Ni(x)Al (x = 0.1-0.95) showing cerium valence fluctuations.

    Science.gov (United States)

    Niehaus, Oliver; Rodewald, Ute Ch; Abdala, Paula M; St Touzani, Rachid; Fokwa, Boniface P T; Janka, Oliver

    2014-03-01

    Members of the solid solution series of CeRu(1-x)Ni(x)Al can be obtained directly by arc melting of the elements. The presented compounds with 0.1 ≤ x ≤ 0.85 crystallize in the orthorhombic space group Pnma (No. 62) in the LaNiAl structure type, while for 0.9 ≤ x ≤ 1, the hexagonal ZrNiAl-type structure is found. The orthorhombic members exhibit an anomaly in the trend of the lattice parameters as well as an interesting behavior of the magnetic susceptibility, suggesting that the cerium cations exhibit no local moment. Besides the mixed-valent nature of the cerium cations, valence fluctuations along with a change in the cerium oxidation state depending on the nickel content have been found. The oxidation state has been determined from the magnetic data and additionally by XANES. Density functional theory calculations have identified the shortest Ce-Ru interaction as decisive for the stability of the orthorhombic solid solution. PMID:24528235

  14. Catalytic ozonation of oxalate with a cerium supported palladium oxide: An efficient degradation not relying on hydroxyl radical oxidation

    KAUST Repository

    Zhang, Tao

    2011-11-01

    The cerium supported palladium oxide (PdO/CeO 2) at a low palladium loading was found very effective in catalytic ozonation of oxalate, a probe compound that is difficult to be efficiently degraded in water with hydroxyl radical oxidation and one of the major byproducts in ozonation of organic matter. The oxalate was degraded into CO 2 during the catalytic ozonation. The molar ratio of oxalate degraded to ozone consumption increased with increasing catalyst dose and decreasing ozone dosage and pH under the conditions of this study. The maximum molar ratio reached around 1, meaning that the catalyst was highly active and selective for oxalate degradation in water. The catalytic ozonation, which showed relatively stable activity, does not promote hydroxyl radical generation from ozone. Analysis with ATR-FTIR and in situ Raman spectroscopy revealed that 1) oxalate was adsorbed on CeO 2 of the catalyst forming surface complexes, and 2) O 3 was adsorbed on PdO of the catalyst and further decomposed to surface atomic oxygen (*O), surface peroxide (*O 2), and O 2 gas in sequence. The results indicate that the high activity of the catalyst is related to the synergetic function of PdO and CeO 2 in that the surface atomic oxygen readily reacts with the surface cerium-oxalate complex. This kind of catalytic ozonation would be potentially effective for the degradation of polar refractory organic pollutants and hydrophilic natural organic matter. © 2011 American Chemical Society.

  15. 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.

  16. 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

  17. 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

  18. 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

  19. 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.

  20. 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

  1. 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.

  2. 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)

  3. 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)

  4. 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.

  5. 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

  6. 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

  7. 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

  8. 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%

  9. 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

  10. 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.

  11. 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.

  12. [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

  13. Amaranth dye in the evaluation of bleaching of cerium (IV) by antioxidants: Application in food and medicinal plants

    Science.gov (United States)

    Nagaraja, Padmarajaiah; Aradhana, Narayanan; Suma, Anandamurthy; Chamaraja, Nelligere Arkeswaraiah; Shivakumar, Anantharaman; Ramya, Kolar Venkatachala

    A simple, low-cost, sensitive, and diversely applicable spectrophotometric method for the determination of total antioxidant capacity of several medicinal plants and food has been developed. The method is based on the bleaching of cerium (IV) by antioxidants and dye in slightly acid medium at room temperature. The unbleached dye, imparting pink color to the solution, is measured at λmax 530 nm which is directly proportional to the antioxidant concentration. The method is reproducible, and the trolox equivalent antioxidant capacities (TEAC coefficients) of the tested antioxidant compounds were correlated with those found by reference method such as ABTS. The recommended method was applied for the determination of total antioxidant capacity of medicinal and food samples. The performance of the recommended method was evaluated in terms of Student's t-test and variance ratio F-test, which indicated the significance of proposed method over the reference method.

  14. 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.

  15. 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

  16. 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)

  17. 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.

  18. 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

  19. STUDY ON ORGANIC LIGHT—RARE—EARTH ADSORBENT—CERIUM BIS(OCTYLPHOSPHATE)

    Institute of Scientific and Technical Information of China (English)

    SuZhengquan; FengHuixia

    1996-01-01

    The tetravalent metal salts of monoalkyl phosphates[M(R-OPO3)2] are a new kind of stationary phases of chromatography-homogeneous bonded phases.The studies on preparation,structure and gas chromatographic efficiency of cerium bis (octylphosphate) (COPP) are reported in this paper. By using chemical analysis,infrared spectra,x-ray diffraction analysis ,the strong evidence that COPP has a layered structure of the α-zirconium phosphate type was demonstrated,the repetitive unit is C8H17OPO3CeO3POC8H17 and there is a little bending or interpenetration of the alkyl chains within the layers.The thermogravimetic analysis of the COPP indicated that it has much more thermalstability than silica-based packings.The thermodynamic parameters ΔH and molecular connectivity indexes x′ for the adsorption of several dozen compounds on the COPP have also been determined by gas chromatographic method,and the fine linearity between them was shown.

  20. Preparation of Nano-TiO2 Doped with Cerium and Its Photocatalytic Activity

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Cerium-doped titanium dioxide nano-powders were prepared through the sol-gel method and the compound samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and UV/Vis diffuse reflectance spectra (DRS). The photocatalytic activity was evaluated by photocatalytic degradation of phenol in water. The results of XRD, TEM, and DRS show that pure TiO2 and Ce-doped TiO2 powder crystallines are a mixture of anatase and rutile;the doping can retard the development of the grain size of TiO2 and decrease the diameter of TiO2 from more than 20nm of pure TiO2 to about 10 nm;the doped TiO2 can improve the light absorption of TiO2 and suitable doping content tends to move the DRS spectrum of TiO2 towards visible light, but too much doping is not good for the light absorption ability.The results of the photocatalytic experiments show that doping with Ce content of 0.08 % ~ 0.4 % can increase the photocatalytic activity of TiO2;however, doping with Ce content of 0.5 % ~ 2.5 % can significantly decrease the photocatalytic activity of TiO2. The favorite doping content is 0.4 % in the range of our experiments.

  1. Physical properties of new cerium palladium phosphide with C6Cr23-type structure

    Directory of Open Access Journals (Sweden)

    T. Abe

    2014-01-01

    Full Text Available We have found that a cerium palladium phosphide crystallizes into a C6Cr23-type structure with atomic disorder. Prepared polycrystalline samples show a homogeneity range in the ternary Ce–Pd–P phase diagram. The physical properties of the highest-quality sample of Ce2.4Pd20.7P5.9 were investigated by measuring the magnetization, electrical resistivity and specific heat. No pronounced phase transition was observed down to 0.5 K. The Kondo screening of localized 4f electrons in metallic Ce2.4Pd20.7P5.9 appears to be weaker than that in the isostructural compounds of Ce3Pd20Si6 and Ce3Pd20Ge6. By a comparative study of Ce2.4Pd20.7P5.9 and Ce3Pd20X6 (X = Si, Ge, the competition between the Kondo temperature and ordering temperatures including the quadrupolar ordering temperature is briefly discussed.

  2. Structure and properties of cerium oxides in bulk and nanoparticulate forms

    Energy Technology Data Exchange (ETDEWEB)

    Gangopadhyay, Shruba [NanoScience Technology Center, University of Central Florida, 12424 Research Parkway, Suite 400, Orlando, FL 32826 (United States); Department of Chemistry, University of Central Florida, 4111 Libra Drive, PS 255, Orlando, FL 32826 (United States); Frolov, Dmitry D. [NanoScience Technology Center, University of Central Florida, 12424 Research Parkway, Suite 400, Orlando, FL 32826 (United States); Department of Chemistry, Moscow M.V. Lomonosov State University, Leninskiye Gory, Moscow 119991 (Russian Federation); Masunov, Artëm E., E-mail: amasunov@ucf.edu [NanoScience Technology Center, University of Central Florida, 12424 Research Parkway, Suite 400, Orlando, FL 32826 (United States); Department of Chemistry, University of Central Florida, 4111 Libra Drive, PS 255, Orlando, FL 32826 (United States); Department of Physics, University of Central Florida, 4111 Libra Drive, PS 430, Orlando, FL 32826 (United States); Seal, Sudipta [Advanced Materials Processing and Analysis Center, University of Central Florida, 12760 Pegasus Drive, ENG1 381, Orlando, FL 32816 (United States); Department of Materials Science and Engineering, University of Central Florida, 12760 Pegasus Drive, ENG1 207, FL 32816 (United States); College of Medicine, University of Central Florida, 6850 Lake Nona Blvd, Orlando, FL 32827 (United States); NanoScience Technology Center, University of Central Florida, 12424 Research Parkway, Suite 400, Orlando, FL 32826 (United States)

    2014-01-25

    The experimental and computational studies on the cerium oxide nanoparticles, as well as stoichiometric phases of bulk ceria are reviewed. Based on structural similarities of these phases in hexagonal aspect, electroneutral and non-polar pentalayers are identified as building blocks of type A sesquioxide structure. The idealized core/shell structure of the ceria nanoparticles is described as dioxide core covered by a single pentalayer of sesquioxide, which explains the exceptional stability of subsurface vacancies in nanoceria. The density functional theory (DFT) predictions of the lattice parameters and elastic moduli for the Ce(IV) and Ce(III) oxides at the hybrid DFT level are also presented. The calculated values for both compounds agree with available experimental data and allow predicting changes in the lattice parameter with decreasing size of the nanoparticles. The lattice parameter is calculated as equilibrium between contraction of sesquioxide structure in the core, and expansion of dioxide structure in the shell of the nanoparticle. This is consistent with available XRD data on ceria NPs obtained in mild aqueous conditions. The core/shell model, however, breaks down when applied to the size dependence of lattice parameter in NPs obtained by the laser ablation techniques.

  3. Structure and properties of cerium oxides in bulk and nanoparticulate forms

    International Nuclear Information System (INIS)

    The experimental and computational studies on the cerium oxide nanoparticles, as well as stoichiometric phases of bulk ceria are reviewed. Based on structural similarities of these phases in hexagonal aspect, electroneutral and non-polar pentalayers are identified as building blocks of type A sesquioxide structure. The idealized core/shell structure of the ceria nanoparticles is described as dioxide core covered by a single pentalayer of sesquioxide, which explains the exceptional stability of subsurface vacancies in nanoceria. The density functional theory (DFT) predictions of the lattice parameters and elastic moduli for the Ce(IV) and Ce(III) oxides at the hybrid DFT level are also presented. The calculated values for both compounds agree with available experimental data and allow predicting changes in the lattice parameter with decreasing size of the nanoparticles. The lattice parameter is calculated as equilibrium between contraction of sesquioxide structure in the core, and expansion of dioxide structure in the shell of the nanoparticle. This is consistent with available XRD data on ceria NPs obtained in mild aqueous conditions. The core/shell model, however, breaks down when applied to the size dependence of lattice parameter in NPs obtained by the laser ablation techniques

  4. 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

  5. Effects of amorphous silica coating on cerium oxide nanoparticles induced pulmonary responses

    Science.gov (United States)

    Ma, Jane; Mercer, Robert R.; Barger, Mark; Schwegler-Berry, Diane; Cohen, Joel M.; Demokritou, Philip; Castranova, Vincent

    2015-01-01

    Recently cerium compounds have been used in a variety of consumer products, including diesel fuel additives, to increase fuel combustion efficiency and decrease diesel soot emissions. However, cerium oxide (CeO2) nanoparticles have been detected in the exhaust, which raises a health concern. Previous studies have shown that exposure of rats to nanoscale CeO2 by intratracheal instillation (IT) induces sustained pulmonary inflammation and fibrosis. In the present study, male Sprague–Dawley rats were exposed to CeO2 or CeO2 coated with a nano layer of amorphous SiO2 (aSiO2/CeO2) by a single IT and sacrificed at various times post-exposure to assess potential protective effects of the aSiO2 coating. The first acellular bronchoalveolar lavage (BAL) fluid and BAL cells were collected and analyzed from all exposed animals. At the low dose (0.15 mg/kg), CeO2 but not aSiO2/CeO2 exposure induced inflammation. However, at the higher doses, both particles induced a dose-related inflammation, cytotoxicity, inflammatory cytokines, matrix metalloproteinase (MMP)-9, and tissue inhibitor of MMP at 1 day post-exposure. Morphological analysis of lung showed an increased inflammation, surfactant and collagen fibers after CeO2 (high dose at 3.5 mg/kg) treatment at 28 days post-exposure. aSiO2 coating significantly reduced CeO2-induced inflammatory responses in the airspace and appeared to attenuate phospholipidosis and fibrosis. Energy dispersive X-ray spectroscopy analysis showed Ce and phosphorous (P) in all particle-exposed lungs, whereas Si was only detected in aSiO2/CeO2-exposed lungs up to 3 days after exposure, suggesting that aSiO2 dissolved off the CeO2 core, and some of the CeO2 was transformed to CePO4 with time. These results demonstrate that aSiO2 coating reduce CeO2-induced inflammation, phospholipidosis and fibrosis. PMID:26210349

  6. Interactive effects of cerium oxide and diesel exhaust nanoparticles on inducing pulmonary fibrosis

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Jane Y.C., E-mail: jym1@cdc.gov [Health Effects Laboratory Division, National Institute for Occupational Safety and Health, Morgantown, WV 26505 (United States); Young, Shih-Houng; Mercer, Robert R.; Barger, Mark; Schwegler-Berry, Diane [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)

    2014-07-15

    Cerium compounds have been used as a fuel-borne catalyst to lower the generation of diesel exhaust particles (DEPs), but are emitted as cerium oxide nanoparticles (CeO{sub 2}) along with DEP in the diesel exhaust. The present study investigates the effects of the combined exposure to DEP and CeO{sub 2} on the pulmonary system in a rat model. Specific pathogen-free male Sprague–Dawley rats were exposed to CeO{sub 2} and/or DEP via a single intratracheal instillation and were sacrificed at various time points post-exposure. This investigation demonstrated that CeO{sub 2} induces a sustained inflammatory response, whereas DEP elicits a switch of the pulmonary immune response from Th1 to Th2. Both CeO{sub 2} and DEP activated AM and lymphocyte secretion of the proinflammatory cytokines IL-12 and IFN-γ, respectively. However, only DEP enhanced the anti-inflammatory cytokine IL-10 production in response to ex vivo LPS or Concanavalin A challenge that was not affected by the presence of CeO{sub 2}, suggesting that DEP suppresses host defense capability by inducing the Th2 immunity. The micrographs of lymph nodes show that the particle clumps in DEP + CeO{sub 2} were significantly larger than CeO{sub 2} or DEP, exhibiting dense clumps continuous throughout the lymph nodes. Morphometric analysis demonstrates that the localization of collagen in the lung tissue after DEP + CeO{sub 2} reflects the combination of DEP-exposure plus CeO{sub 2}-exposure. At 4 weeks post-exposure, the histological features demonstrated that CeO{sub 2} induced lung phospholipidosis and fibrosis. DEP induced lung granulomas that were not significantly affected by the presence of CeO{sub 2} in the combined exposure. Using CeO{sub 2} as diesel fuel catalyst may cause health concerns. - Highlights: • DEP induced acute lung inflammation and switched immune response from Th1 to Th2. • DEP induced lung granulomas were not affected by the presence of CeO{sub 2}. • CeO{sub 2} induced sustained lung

  7. Interactive effects of cerium oxide and diesel exhaust nanoparticles on inducing pulmonary fibrosis

    International Nuclear Information System (INIS)

    Cerium compounds have been used as a fuel-borne catalyst to lower the generation of diesel exhaust particles (DEPs), but are emitted as cerium oxide nanoparticles (CeO2) along with DEP in the diesel exhaust. The present study investigates the effects of the combined exposure to DEP and CeO2 on the pulmonary system in a rat model. Specific pathogen-free male Sprague–Dawley rats were exposed to CeO2 and/or DEP via a single intratracheal instillation and were sacrificed at various time points post-exposure. This investigation demonstrated that CeO2 induces a sustained inflammatory response, whereas DEP elicits a switch of the pulmonary immune response from Th1 to Th2. Both CeO2 and DEP activated AM and lymphocyte secretion of the proinflammatory cytokines IL-12 and IFN-γ, respectively. However, only DEP enhanced the anti-inflammatory cytokine IL-10 production in response to ex vivo LPS or Concanavalin A challenge that was not affected by the presence of CeO2, suggesting that DEP suppresses host defense capability by inducing the Th2 immunity. The micrographs of lymph nodes show that the particle clumps in DEP + CeO2 were significantly larger than CeO2 or DEP, exhibiting dense clumps continuous throughout the lymph nodes. Morphometric analysis demonstrates that the localization of collagen in the lung tissue after DEP + CeO2 reflects the combination of DEP-exposure plus CeO2-exposure. At 4 weeks post-exposure, the histological features demonstrated that CeO2 induced lung phospholipidosis and fibrosis. DEP induced lung granulomas that were not significantly affected by the presence of CeO2 in the combined exposure. Using CeO2 as diesel fuel catalyst may cause health concerns. - Highlights: • DEP induced acute lung inflammation and switched immune response from Th1 to Th2. • DEP induced lung granulomas were not affected by the presence of CeO2. • CeO2 induced sustained lung inflammation, phospholipidosis, and fibrosis. • After the combined exposure, CeO2 and

  8. Freshwater dispersion stability of PAA-stabilised cerium oxide nanoparticles and toxicity towards Pseudokirchneriella subcapitata

    Energy Technology Data Exchange (ETDEWEB)

    Booth, Andy, E-mail: andy.booth@sintef.no [SINTEF Materials and Chemistry, Trondheim N-7465 (Norway); Størseth, Trond [SINTEF Materials and Chemistry, Trondheim N-7465 (Norway); Altin, Dag [BioTrix, Trondheim N-7022 (Norway); Fornara, Andrea; Ahniyaz, Anwar [German Federal Institute for Risk Assessment (BfR), Department of Product Safety, Berlin (Germany); Jungnickel, Harald; Laux, Peter; Luch, Andreas [SP Chemistry, Materials and Surfaces, Drottning Kristinas vag 45, SE-11686 Stockholm (Sweden); Sørensen, Lisbet [SINTEF Materials and Chemistry, Trondheim N-7465 (Norway)

    2015-02-01

    An aqueous dispersion of poly (acrylic acid)-stabilised cerium oxide (CeO{sub 2}) nanoparticles (PAA-CeO{sub 2}) was evaluated for its stability in a range of freshwater ecotoxicity media (MHRW, TG 201 and M7), with and without natural organic matter (NOM). In a 15 day dispersion stability study, PAA-CeO{sub 2} did not undergo significant aggregation in any media type. Zeta potential varied between media types and was influenced by PAA-CeO{sub 2} concentration, but remained constant over 15 days. NOM had no influence on PAA-CeO{sub 2} aggregation or zeta potential. The ecotoxicity of the PAA-CeO{sub 2} dispersion was investigated in 72 h algal growth inhibition tests using the freshwater microalgae Pseudokirchneriella subcapitata. PAA-CeO{sub 2} EC{sub 50} values for growth inhibition (GI; 0.024 mg/L) were 2–3 orders of magnitude lower than pristine CeO{sub 2} EC{sub 50} values reported in the literature. The concentration of dissolved cerium (Ce{sup 3+}/Ce{sup 4+}) in PAA-CeO{sub 2} exposure suspensions was very low, ranging between 0.5 and 5.6 μg/L. Free PAA concentration in the exposure solutions (0.0096–0.0384 mg/L) was significantly lower than the EC{sub 10} growth inhibition (47.7 mg/L) value of pure PAA, indicating that free PAA did not contribute to the observed toxicity. Elemental analysis indicated that up to 38% of the total Cerium becomes directly associated with the algal cells during the 72 h exposure. TOF-SIMS analysis of algal cell wall compounds indicated three different modes of action, including a significant oxidative stress response to PAA-CeO{sub 2} exposure. In contrast to pristine CeO{sub 2} nanoparticles, which rapidly aggregate in standard ecotoxicity media, PAA-stabilised CeO{sub 2} nanoparticles remain dispersed and available to water column species. Interaction of PAA with cell wall components, which could be responsible for the observed biomarker alterations, could not be excluded. This study indicates that the increased

  9. 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.

  10. 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.

  11. 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

  12. 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)

  13. 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

  14. 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)

  15. 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

  16. 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

  17. 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.

  18. 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

  19. 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

  20. 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 ...

  1. 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...

  2. 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 ...

  3. 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)

  4. 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...

  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. Reinforcement of natural rubber latex with silica modified by cerium oxide:preparation and properties

    Institute of Scientific and Technical Information of China (English)

    张福全; 廖禄生; 王永周; 汪月琼; 黄红海; 李普旺; 彭政; 曾日中

    2016-01-01

    Variable masses of nano cerium oxide (CeO2) were added into nano silica (SiO2) to prepare the well-dispersed SiO2-CeO2 suspension (SiO2-CeO2), cetyltrimethyl ammonium bromide (CTAB) was used to adjust the compatibility of SiO2-CeO2 with rubber matrix, then SiO2-CeO2 modified by CTAB and curing formulas were mixed with fresh natural rubber (NR) latex to prepare NR/SiO2-CeO2 nanocomposites that contained 0–10 parts of CeO2 by a new emulsion compounding method. The morphologies, cure characteristics, mechanical properties and thermal-oxidative stability of NR/SiO2-CeO2 nanocomposites were investigated. The re-sults revealed that the presence of CeO2 in NR/SiO2-CeO2nanocomposites was favorable for enhancing the interaction between NR matrix and fillers, helped to get smaller SiO2-CeO2 particles with narrower particle size distribution, further improved the crosslink densities and mechanical properties of NR/SiO2-CeO2 nanocomposites vulcanizates. Meanwhile, the addition of CeO2 increased the active energy at least 4.66%, obviously improved the thermal-oxidative aging-inhibiting properties of NR/SiO2-CeO2 nanocomposites. Additionally, nanocomposites containing CeO2 promotedTg shift to high temperature direction, causing the nanocomposites featured higher tanδ at 0 ºC and lower tanδ at 60 ºC and exhibited comparable wet grip and lower rolling resistance when NR/SiO2-CeO2nano-composites were used in tire tread compound.

  13. 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

  14. The effect of cerium and lanthanum surface treatments on early stages of oxidation of A361 aluminium alloy at high temperature

    International Nuclear Information System (INIS)

    X-ray photoelectron spectroscopy analysis has been used to study the surface of A361 aluminium alloy after electrodeposition of cerium and lanthanum compounds followed by oxidation tests in air at 100-500 deg. C for 2 h. Cerium and lanthanum oxide deposits are found on the β-AlFeSi second phase particles and to a lesser extent on the eutectic Al-Si areas, while the α-Al phase is covered with a thin aluminium oxide film. This uneven deposition may be related either to a preferential nucleation and growth process on active interfaces or to the differing electrical conductivity of the phases and intermetallic compounds of the alloy. Initial stages of oxidation of A361 alloy disclosed thickening of the aluminium oxide layer and Mg enrichment at the surface, especially above 400 deg. C. Rare earth deposits revealed two different effects: reduced Mg diffusion and enhanced thickening of the aluminium oxide film. A distinctive behaviour of Ce oxide appears at 300-500 deg. C related with Ce(III) to Ce(IV) transition

  15. The effect of cerium and lanthanum surface treatments on early stages of oxidation of A361 aluminium alloy at high temperature

    Science.gov (United States)

    Pardo, A.; Feliú, S.; Merino, M. C.; Arrabal, R.; Matykina, E.

    2007-11-01

    X-ray photoelectron spectroscopy analysis has been used to study the surface of A361 aluminium alloy after electrodeposition of cerium and lanthanum compounds followed by oxidation tests in air at 100-500 °C for 2 h. Cerium and lanthanum oxide deposits are found on the β-AlFeSi second phase particles and to a lesser extent on the eutectic Al-Si areas, while the α-Al phase is covered with a thin aluminium oxide film. This uneven deposition may be related either to a preferential nucleation and growth process on active interfaces or to the differing electrical conductivity of the phases and intermetallic compounds of the alloy. Initial stages of oxidation of A361 alloy disclosed thickening of the aluminium oxide layer and Mg enrichment at the surface, especially above 400 °C. Rare earth deposits revealed two different effects: reduced Mg diffusion and enhanced thickening of the aluminium oxide film. A distinctive behaviour of Ce oxide appears at 300-500 °C related with Ce(III) to Ce(IV) transition.

  16. New Cerium(III Complex Of Schiff Base (E-N-Benzylidene-4-Methoxyaniline: Synthesis And Density Functional Theoretical Study Of Vibrational Spectra

    Directory of Open Access Journals (Sweden)

    Imanelakehal

    2016-05-01

    Full Text Available Complex of cerium (III with (E-N-benzylidene-4-methoxyaniline is synthesized through a one-pot three-componentreaction from aromatical dehyde, aromatic amine and the CeCl3· 7 H2O, as an efficient catalyst. This cerium(IIIcom- plexis characterized by IR, 1H, and 13 CNMR-spectros copy and mass-spectraldata. Molecular structure, Mullikan charges, thermodynamic parameters; vibrational frequencies and intensities were calculated by Density Functional theory methods (B3LYP,B3PW91,mPW1PW91 and PBEPBE using the SDD basis set. The comparison between the calculated and experimental data inorder to attain the best quality and to predict the structure, the best perfor-mance in the vibration spectra perfected of the title compound,we have found that the harmonic vibration computed are in a good agreement with the observed in IRspectrum, for closest match we calculated optimal scaling factors can recommend for the IR spectral future predictions for unknown compounds of this class. In order to better comparison, we also root meansqu are values of the experimental and calculated IR bands are 16.64,16.64,17.45,17.66 and the mean absolute percentage error values are1.33,1.39,1.40, and 1.5forB3LYP, B3PW91,mPW1PW91, and PBEPBE methods respectively

  17. Acute changes in murine hippocampus and olfactory bulb after nasal instillation of varying size cerium dioxide particles.

    Science.gov (United States)

    Liu, Yang; Li, Yuanyuan; Yang, Tongwang; Yang, Jing; Wang, He; Wu, Gang

    2016-01-01

    Cerium (Ce)-containing compounds are now widely applied in medicine, agriculture, and animal breeding. However, the effects of Ce on humans, especially on the central nervous system (CNS), remain to be determined. In order to investigate whether Ce exposure affected the CNS, the aim of this study was to expose female ICR mice to varying nanoparticle sizes of 35 nm and 300 nm, and to a mixture of 1-5 µM cerium dioxide (CeO2) particles through intranasal (i.n.) instillation at daily dose of 40 mg/kg body weight. Immunohistochemical data showed that glial fibrillary acidic protein expression (GFAP) increased significantly in the hippocampus and olfactory bulb in all Ce-administered groups. The ultrastructure of olfactory bulb cells displayed chromatin reduction. In the hippocampus decreased chromatin was associated with ribosome shedding as evidenced from transmission electron microscopy (TEM). No significant differences in immunohistochemistry were noted between varying sizes of CeO2 groups. The results of inductively coupled plasma-mass spectroscopy (ICP-MS) analysis group exposed to 1-5 µM demonstrated that Ce levels were significantly higher in whole brain (0.17 ng/mg) than for the control (0.04 ng/mg). Data thus demonstrated that i.n. instillation of different sized CeO2 particles induced damage in the olfactory bulb and hippocampus and that CeO2 particle size did not appear to play a role in the observed adverse responses. PMID:27599233

  18. Themoelectromotive force and electroconductivity of Ce-M-Si system compounds (M=Fe, Co, Ni)

    International Nuclear Information System (INIS)

    Measuring results of temperature dependences of the differential thermo- e.m.f. and electric conductivity of some compounds of Ce-M-Si systems (M=Fe, Co, Ni) are presented. Anomalies observed of kinetic coefficients of the majority of compound under investigation are supposed to be stipulated by s-f-hybridization resulting from the presence of cerium 4f-states near the Fermi level

  19. Extraction of cerium (III) by polymer gels swollen with bidentate organophosphorus compounds

    International Nuclear Information System (INIS)

    The extraction of Ce (III) from aqueous solutions containing Al (NO3)3 was examined by using styrene-divinylbenzene copolymer (SDB) gels swollen with dihexyl-N, N-diethylcarbamoylmethylphosphonate (CMP), octyl(phenyl)-N, N-diisobutylcarbamoylmethylphosphine oxide (CMPO) and an equimolar mixture of CMP and CMPO. The extraction constants (Kex) for the gels with CMP and CMPO were evaluated. The distribution ratio of Ce (III) for the gel with an equimolar mixture of CMP and CMPO was described as Kd = (KexCMP [CMP]3 + KexCMPO [CMPO]3) [NO3-]3 by using these extraction constants. The extraction rate was found to be controlled by diffusion of Ce-complex [Ce(NO3)3 (CMPO)3 or Ce(NO3)3 (CMP)3] through the gel. The diffusion coefficient (Ds) was inversely proportional to the viscosity of extractant (η) and represented by an expression similar to the Stokes-Einstein equation, Dsη/T = constant. A decrease in the viscosity of extractant was effective for increasing the extraction rate. (author)

  20. Sensitizing effect of cerium (4) sulfate on photooxidation of organic compounds in aqueous solutions

    International Nuclear Information System (INIS)

    Influence of Ce(SO4)2 addition on the photooxidation rate of organic substances in aqueous solutions has been discussed. It is shown that to a certain value, the rate constant of oxalic acid oxidation increases linearly with increasing oxidant amount. Using a combination of chemical and photochemical oxidation of oxalic acid in aqueous solution with Ce(SO4)2 as a sensitizer, one can increase the oxidation rate by a factor of 45 and to reduce the time required for carbon determination in aqueous solutions from 4-5 hours down to 8-9 min

  1. 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

  2. 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.

  3. 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.

  4. 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.

  5. 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

  6. 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)

  7. 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)

  8. 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

  9. 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.

  10. 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.

  11. 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

  12. 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

  13. 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.)

  14. 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.)

  15. 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.

  16. 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?

  17. 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

  18. 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)

  19. 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.

  20. 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

  1. 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

  2. Corrosion and protection of heterogeneous cast Al-Si (356) and Al-Si-Cu-Fe (380) alloys by chromate adn cerium inhibitors

    Science.gov (United States)

    Jain, Syadwad

    In this study, the localized corrosion and conversion coating on cast alloys 356 (Al-7.0Si-0.3Mg) and 380 (Al-8.5Si-3.5Cu-1.6Fe) were characterized. The intermetallic phases presence in the permanent mold cast alloy 356 are primary-Si, Al5FeSi, Al8Si6Mg3Fe and Mg2Si. The die cast alloy 380 is rich in Cu and Fe elements. These alloying elements result in formation of the intermetallic phases Al 5FeSi, Al2Cu and Al(FeCuCr) along with primary-Si. The Cu- and Fe-rich IMPS are cathodic with respect to the matrix phase and strongly govern the corrosion behavior of the two cast alloys in an aggressive environment due to formation of local electrochemical cell in their vicinity. Results have shown that corrosion behavior of permanent mould cast alloy 356 is significantly better than the die cast aluminum alloy 380, primarily due to high content of Cu- and Fe-rich phases such as Al2Cu and Al 5FeSi in the latter. The IMPS also alter the protection mechanism of the cast alloys in the presence of inhibitors in an environment. The presence of chromate in the solution results in reduced cathodic activity on all the phases. Chromate provides some anodic inhibition by increasing pitting potentials and altering corrosion potentials for the phases. Results have shown that performance of CCC was much better on 356 than on 380, primarily due to inhomogeneous and incomplete coating deposition on Cu- and Fe- phases present in alloy 380. XPS and Raman were used to characterize coating deposition on intermetallics. Results show evidence of cyanide complex formation on the intermetallic phases. The presence of this complex is speculated to locally suppress CCC formation. Formation and breakdown of cerium conversion coatings on 356 and 380 was also analyzed. Results showed that deposition of cerium hydroxide started with heavy precipitation on intermetallic particles with the coatings growing outwards onto the matrix. Electrochemical analysis of synthesized intermetallics compounds in the

  3. 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.

  4. 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)

  5. 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.

  6. 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.

  7. 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.

  8. 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)

  9. 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.

  10. 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.

  11. 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.

  12. 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 %

  13. 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.

  14. 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%

  15. 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.

  16. 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

  17. [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

  18. 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.

  19. 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.

  20. 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.

  1. 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.

  2. 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.

  3. 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

  4. 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.

  5. 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

  6. 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

  7. 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.

  8. 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.

  9. 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

  10. 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)

  11. 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...

  12. 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

  13. 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)

  14. 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.

  15. 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.

  16. 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)

  17. 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

  18. 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

  19. 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.

  20. 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.

  1. 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

  2. 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)

  3. 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

  4. Demonstration of enhanced K-edge angiography using a cerium target x-ray generator

    International Nuclear Information System (INIS)

    The cerium target x-ray generator is useful in order to perform enhanced K-edge angiography using a cone beam because K-series characteristic x rays from the cerium target are absorbed effectively by iodine-based contrast mediums. The x-ray generator consists of a main controller, a unit with a Cockcroft-Walton circuit and a fixed anode x-ray tube, 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 1.0x1.3 mm. Cerium Kα lines were left using a barium sulfate filter, and the x-ray intensity was 0.48 μC/kg at 1.0 m from the source with a tube voltage of 60 kV, a current of 0.40 mA, and an exposure time of 1.0 s. Angiography was performed with a computed radiography system using iodine-based microspheres. In coronary angiography of nonliving animals, we observed fine blood vessels of approximately 100 μm with high contrasts

  5. Influences of the main anodic electroplating parameters on cerium oxide films

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Yang; Yang, Yumeng; Du, Xiaoqing; Chen, Yu [Department of Chemistry, Zhejiang University, Hangzhou 310027, Zhejiang (China); Zhang, Zhao, E-mail: eaglezzy@zjuem.zju.edu.cn [Department of Chemistry, Zhejiang University, Hangzhou 310027, Zhejiang (China); Zhang, Jianqing [Department of Chemistry, Zhejiang University, Hangzhou 310027, Zhejiang (China); State Key Laboratory for Corrosion and Protection of Metals, Shenyang 110016 (China)

    2014-06-01

    Cerium oxide thin films were fabricated onto 316 L stainless steel via a potentiostatically anodic electrodeposition approach in the solutions containing cerium(III) nitrate (0.05 M), ammonia acetate (0.1 M) and ethanol (10% V/V). The electrochemical behaviors and deposition parameters (applied potential, bath temperature, dissolving O{sub 2} and bath pH) have been investigated. Results show that, the electrochemical oxidation of Ce{sup 3+} goes through one electrochemical step, which is under charge transfer control. The optimum applied potential for film deposition is 0.8 V. Bath temperature plays a significant effect on the deposition rate, composition (different colors of the film) and surface morphology of the deposits. Due to the hydrolysis of Ce{sup 3+}, cerous hydroxide is facility to form when the bath temperature is higher than 60 °C. The electroplating bath pH is another key role for the anodic deposition of cerium oxide thin films, and the best bath pH is around 6.20. N{sub 2} or O{sub 2} purged into the bath will result in film porosities and O{sub 2} favors cerium oxide particles and film generation.

  6. Influences of the main anodic electroplating parameters on cerium oxide films

    International Nuclear Information System (INIS)

    Cerium oxide thin films were fabricated onto 316 L stainless steel via a potentiostatically anodic electrodeposition approach in the solutions containing cerium(III) nitrate (0.05 M), ammonia acetate (0.1 M) and ethanol (10% V/V). The electrochemical behaviors and deposition parameters (applied potential, bath temperature, dissolving O2 and bath pH) have been investigated. Results show that, the electrochemical oxidation of Ce3+ goes through one electrochemical step, which is under charge transfer control. The optimum applied potential for film deposition is 0.8 V. Bath temperature plays a significant effect on the deposition rate, composition (different colors of the film) and surface morphology of the deposits. Due to the hydrolysis of Ce3+, cerous hydroxide is facility to form when the bath temperature is higher than 60 °C. The electroplating bath pH is another key role for the anodic deposition of cerium oxide thin films, and the best bath pH is around 6.20. N2 or O2 purged into the bath will result in film porosities and O2 favors cerium oxide particles and film generation.

  7. Influences of the main anodic electroplating parameters on cerium oxide films

    Science.gov (United States)

    Yang, Yang; Yang, Yumeng; Du, Xiaoqing; Chen, Yu; Zhang, Zhao; Zhang, Jianqing

    2014-06-01

    Cerium oxide thin films were fabricated onto 316 L stainless steel via a potentiostatically anodic electrodeposition approach in the solutions containing cerium(III) nitrate (0.05 M), ammonia acetate (0.1 M) and ethanol (10% V/V). The electrochemical behaviors and deposition parameters (applied potential, bath temperature, dissolving O2 and bath pH) have been investigated. Results show that, the electrochemical oxidation of Ce3+ goes through one electrochemical step, which is under charge transfer control. The optimum applied potential for film deposition is 0.8 V. Bath temperature plays a significant effect on the deposition rate, composition (different colors of the film) and surface morphology of the deposits. Due to the hydrolysis of Ce3+, cerous hydroxide is facility to form when the bath temperature is higher than 60 °C. The electroplating bath pH is another key role for the anodic deposition of cerium oxide thin films, and the best bath pH is around 6.20. N2 or O2 purged into the bath will result in film porosities and O2 favors cerium oxide particles and film generation.

  8. Photochemical precipitation of thorium and cerium and their separation from other ions in aqueous solution.

    Science.gov (United States)

    Das, M; Heyn, A H; Hoffman, M Z; Agarwal, R P

    1970-10-01

    Thorium was precipitated from homogeneous solution by exposing solutions of thorium and periodate in dilute perchloric acid to 253.7 nm radiation from a low-pressure mercury lamp. Periodate is reduced photochemically to iodate which causes the formation of a dense precipitate of the basic iodate of thorium(IV). The precipitate was redissolved, the iodate reduced, the thorium precipitated first as the hydroxide, then as the oxalate and ignited to the dioxide for weighing. Thorium(IV) solutions containing 8-200 mg of ThO(2) gave quantitative results with a standard deviation (s) of 0.2 mg. Separations from 25 mg each of iron, calcium, magnesium, 50 mg of yttrium and up to 500 mg of uranium(VI) were quantitative (s = 0.25 mg). Separations from rare earths, except cerium, were accomplished by using hexamethylenetetramine rather than ammonia for the precipitation of the hydroxide. Cerium(III) was similarly precipitated and converted into CeO(2) for weighing. Quantitative results were obtained for 13-150 mg of CeO(2) with a standard deviation of 0.2 mg. Separations from 200 mg of uranium were quantitative. Other rare earths and yttrium interfered seriously. The precipitates of the basic cerium(IV) and thorium iodates obtained are more compact than those obtained by direct precipitation and can be handled easily. Attempts to duplicate Suzuki's method for separating cerium from neodymium and yttrium were not successful. PMID:18960820

  9. Excimer Laser Deposition and Characterization of Cerium Doped TiO2

    Czech Academy of Sciences Publication Activity Database

    Fajgar, Radek; Dřínek, Vladislav; Kupčík, Jaroslav; Šubrt, Jan; Murafa, Nataliya

    - : -, 2011, s. 131. ISSN N. [EuroCVD 18. Kinsale, Co. Cork (IE), 04.09.2011-09.09.2011] Institutional research plan: CEZ:AV0Z40720504; CEZ:AV0Z40320502 Keywords : laser deposition * TiO2 * cerium Subject RIV: CH - Nuclear ; Quantum Chemistry

  10. Transient Dynamics of Fluoride-Based High Concentration Erbium/Cerium Co-Doped Fiber Amplifier

    Institute of Scientific and Technical Information of China (English)

    S. S-H. Yam; Y. Akasaka; Y. Kubota; R. Huang; D. L. Harris; J. Pan

    2003-01-01

    We designed and evaluated a fluoride-based high concentration erbium/ cerium co-doped fiber amplifier. It is suitable for Metropolitan Area Networks due to faster transient, flatter (unfiltered) gain, smaller footprint and gain excursion than its silica-based counterpart.

  11. Separation of cerium from high level waste solution of Purex origin

    International Nuclear Information System (INIS)

    A simple solvent extraction procedure for the separation of 144Ce from Purex high level waste (HLW) is described. 2-ethylhexyl 2-ethylhexyl phosphonic acid (KSM-17) has been used as extractant. About 10 mCi of cerium was separated from HLW using this technique. This method is amenable for automation and scale up. (author)

  12. Cerium oxide coated anodes for aluminum electrowinning: Topical report, October 1, 1986-June 30, 1987

    Energy Technology Data Exchange (ETDEWEB)

    Walker, J. K.

    1987-12-01

    Because of the cost of building and maintaining a carbon anode plant and the energy penalties associated with the use of carbon anodes in the production of aluminum, the use of inert anodes has long been proposed. Various cermet anodes have been investigated. In this paper, tests on a material, cerium oxyfluoride (CEROX), deposited in situ as an anode, are reported. (JDH)

  13. Growth and characterization of Sm3+ doped cerium oxalate single crystals

    Directory of Open Access Journals (Sweden)

    Minu Mary C

    2016-07-01

    Full Text Available Single crystals of Sm3+ doped cerium oxalate decahydrate were synthesized using single diffusion gel technique and the conditions influencing the size, morphology, nucleation density and quality of the crystals were optimized. Highly transparent single crystals of average size 3 mm × 2 mm × 1 mm with well-defined hexagonal morphology were grown during a time period of two weeks. X-ray powder diffraction analysis revealed that the grown crystals crystallize in the monoclinic system with space group P21/c as identical with the pure cerium oxalate. The various functional groups of the oxalate ligand and the water of crystallization were identified by Fourier transform infrared spectroscopy. The photoluminescence spectrum of the Sm3+ doped cerium oxalate indicated that the Sm3+ ions are optically active in the cerium oxalate matrix. The crystal has a strong and efficient orange red emission with a wavelength peak at 595 nm and hence can be effectively used for optical amplification. Microhardness measurements of the crystal revealed that they belong to the soft material category.

  14. EXAFS and XANES analysis of plutonium and cerium edges from titanate ceramics for fissile materials disposal

    International Nuclear Information System (INIS)

    We report x-ray absorption near edge structure (XANES) and extended x-ray absorption fine structure (EXAFS) spectra from the plutonium LIII edge and XANES from the cerium LII edge in prototype titanate ceramic hosts. The titanate ceramics studied are based upon the hafnium-pyrochlore and zirconolite mineral structures and will serve as an immobilization host for surplus fissile materials, containing as much as 10 weight % fissile plutonium and 20 weight % (natural or depleted) uranium. Three ceramic formulations were studied: one employed cerium as a ''surrogate'' element, replacing both plutonium and uranium in the ceramic matrix, another formulation contained plutonium in a ''baseline'' ceramic formulation, and a third contained plutonium in a formulation representing a high-impurity plutonium stream. The cerium XANES from the surrogate ceramic clearly indicates a mixed III-IV oxidation state for the cerium. In contrast, XANES analysis of the two plutonium-bearing ceramics shows that the plutonium is present almost entirely as Pu(IV) and occupies the calcium site in the zirconolite and pyrochlore phases. The plutonium EXAFS real-space structure shows a strong second-shell peak, clearly distinct from that of PuO2, with remarkably little difference in the plutonium crystal chemistry indicated between the baseline and high-impurity formulations

  15. Cerium oxide nanoparticles inhibit lipopolysaccharide induced MAP kinase/NF-kB mediated severe sepsis

    Directory of Open Access Journals (Sweden)

    Vellaisamy Selvaraj

    2015-09-01

    Full Text Available The life threatening disease of sepsis is associated with high mortality. Septic patient survivability with currently available treatments has failed to improve. The purpose of this study was to evaluate whether lipopolysaccharide (LPS induced sepsis mortality and associated hepatic dysfunction can be prevented by cerium oxide nanoparticles (CeO2NPs treatment in male Sprague Dawley rats. Here we provide the information about the methods processing of raw data related to our study published in Biomaterials (Selvaraj et al., Biomaterials, 2015, In press and Data in Brief (Selvaraj et al., Data in Brief, 2015, In Press. The data present here provides confirmation of cerium oxide nanoparticle treatments ability to prevent the LPS induced sepsis associated changes in physiological, blood cell count, inflammatory protein and growth factors in vivo. In vitro assays investigation the treated of macrophages cells with different concentrations of cerium oxide nanoparticle demonstrate that concentration of cerium oxide nanoparticles below 1 µg/ml did not significantly influence cell survival as determined by the MTT assay.

  16. Cerium oxide nanoparticles inhibit lipopolysaccharide induced MAP kinase/NF-kB mediated severe sepsis.

    Science.gov (United States)

    Selvaraj, Vellaisamy; Nepal, Niraj; Rogers, Steven; Manne, Nandini D P K; Arvapalli, Ravikumar; Rice, Kevin M; Asano, Shinichi; Fankenhanel, Erin; Ma, J Y; Shokuhfar, Tolou; Maheshwari, Mani; Blough, Eric R

    2015-09-01

    The life threatening disease of sepsis is associated with high mortality. Septic patient survivability with currently available treatments has failed to improve. The purpose of this study was to evaluate whether lipopolysaccharide (LPS) induced sepsis mortality and associated hepatic dysfunction can be prevented by cerium oxide nanoparticles (CeO2NPs) treatment in male Sprague Dawley rats. Here we provide the information about the methods processing of raw data related to our study published in Biomaterials (Selvaraj et al., Biomaterials, 2015, In press) and Data in Brief (Selvaraj et al., Data in Brief, 2015, In Press). The data present here provides confirmation of cerium oxide nanoparticle treatments ability to prevent the LPS induced sepsis associated changes in physiological, blood cell count, inflammatory protein and growth factors in vivo. In vitro assays investigation the treated of macrophages cells with different concentrations of cerium oxide nanoparticle demonstrate that concentration of cerium oxide nanoparticles below 1 µg/ml did not significantly influence cell survival as determined by the MTT assay. PMID:26217772

  17. Phenotypic and genomic responses to titanium dioxide and cerium oxide nanoparticles in Arabidopsis germinants

    Science.gov (United States)

    The effects of exposure to two nanoparticles (NPs) -titanium dioxide (nano-titania) and cerium oxide (nano-ceria) at 500 mg NPs L-1 on gene expression and growth in Arabidopsis thaliana germinants were studied using microarrays and phenotype studies. After 12 days post treatment,...

  18. Performance of Platinum and Gold Catalysts Supported on Ceria-zirconia Mixed Oxide in the Total Oxidation of Model Volatile Organic Compounds

    Czech Academy of Sciences Publication Activity Database

    Topka, Pavel; Kaluža, Luděk

    - : -, 2014, -. [Fundamentals and Applications of Cerium Dioxide in Catalysis. Udine (IT), 11.07.2014-14.07.2014] R&D Projects: GA ČR GP13-24186P Institutional support: RVO:67985858 Keywords : volatile organic compounds * platinum * ceria Subject RIV: CF - Physical ; Theoretical Chemistry http://ceria.cism.it/abstract.html

  19. Magnetic hysteresis of cerium doped bismuth ferrite thin films

    International Nuclear Information System (INIS)

    The influence of Cerium doping on the structural and magnetic properties of BiFeO3 thin films have been investigated. Rietveld refinement of X-ray diffraction data and successive de-convolution of Raman scattering spectra of Bi1−xCexFeO3 (BCFO) thin films with x=0–0.20 reflect the single phase rhombohedral (R3c) formation for x<0.08, whereas concentration-driven gradual structural phase transition from rhombohedral (R3c) to partial tetragonal (P4mm) phase follows for x≥0.08. All low wavenumber Raman modes (<300 cm−1) showed a noticeable shift towards higher wavenumber with increase in doping concentration, except Raman E-1 mode (71 cm−1), shows a minor shift. Sudden evolution of Raman mode at 668 cm−1, manifested as A1-tetragonal mode, accompanied by the shift to higher wavenumber with increase in doping concentration (x) affirm partial structural phase transition. Anomalous wasp waist shaped (M–H) hysteresis curves with improved saturation magnetization (Ms) for BCFO thin films is attributed to antiferromagnetic interaction/hybridization between Ce 4f and Fe 3d electronic states. The contribution of both hard and soft phase to the total coercivity is calculated. Polycrystalline Bi0.88Ce0.12FeO3 thin film found to exhibit better magnetic properties with Ms=15.9 emu/g without any impure phase. - Highlights: • Synthesis of single phase Bi1−xCexFeO3 thin films with (x=0–0.2) on cost effective corning glass and silicon substrates using CSD technique. • Structural modification studies using Rietveld refinement of XRD and de-convolution of Raman spectra revealed partial phase transition from rhombohedral (R3c) to tetragonal (P4mm) phase. • Possible reasons for origin of pinched magnetic behavior of BCFO thin films are identified. • Contribution of both hard and soft magnetic phase in coercivity of BCFO thin films is calculated and practical applications of such materials exhibiting pinching behavior are conferred

  20. Magnetic hysteresis of cerium doped bismuth ferrite thin films

    Energy Technology Data Exchange (ETDEWEB)

    Gupta, Surbhi [Department of Physics and Astrophysics, University of Delhi (India); Tomar, Monika [Physics Department, Miranda House, University of Delhi (India); Gupta, Vinay, E-mail: drguptavinay@gmail.com [Department of Physics and Astrophysics, University of Delhi (India)

    2015-03-15

    The influence of Cerium doping on the structural and magnetic properties of BiFeO{sub 3} thin films have been investigated. Rietveld refinement of X-ray diffraction data and successive de-convolution of Raman scattering spectra of Bi{sub 1−x}Ce{sub x}FeO{sub 3} (BCFO) thin films with x=0–0.20 reflect the single phase rhombohedral (R3c) formation for x<0.08, whereas concentration-driven gradual structural phase transition from rhombohedral (R3c) to partial tetragonal (P4mm) phase follows for x≥0.08. All low wavenumber Raman modes (<300 cm{sup −1}) showed a noticeable shift towards higher wavenumber with increase in doping concentration, except Raman E-1 mode (71 cm{sup −1}), shows a minor shift. Sudden evolution of Raman mode at 668 cm{sup −1}, manifested as A{sub 1}-tetragonal mode, accompanied by the shift to higher wavenumber with increase in doping concentration (x) affirm partial structural phase transition. Anomalous wasp waist shaped (M–H) hysteresis curves with improved saturation magnetization (M{sub s}) for BCFO thin films is attributed to antiferromagnetic interaction/hybridization between Ce 4f and Fe 3d electronic states. The contribution of both hard and soft phase to the total coercivity is calculated. Polycrystalline Bi{sub 0.88}Ce{sub 0.12}FeO{sub 3} thin film found to exhibit better magnetic properties with M{sub s}=15.9 emu/g without any impure phase. - Highlights: • Synthesis of single phase Bi{sub 1−x}Ce{sub x}FeO{sub 3} thin films with (x=0–0.2) on cost effective corning glass and silicon substrates using CSD technique. • Structural modification studies using Rietveld refinement of XRD and de-convolution of Raman spectra revealed partial phase transition from rhombohedral (R3c) to tetragonal (P4mm) phase. • Possible reasons for origin of pinched magnetic behavior of BCFO thin films are identified. • Contribution of both hard and soft magnetic phase in coercivity of BCFO thin films is calculated and practical

  1. The nature of the surface film on steel treated with cerium and lanthanum cinnamate based corrosion inhibitors

    Energy Technology Data Exchange (ETDEWEB)

    Blin, Frederic [School of Physics and Materials Engineering, Centre for Green Chemistry, Monash University, Wellington Road, Clayton 3800, Victoria (Australia)]. E-mail: frederic.blin@spme.monash.edu.au; Leary, Stuart G. [School of Chemistry, Centre for Green Chemistry, Monash University, Wellington Road, Clayton 3800, Victoria (Australia); Deacon, Glen B. [School of Chemistry, Centre for Green Chemistry, Monash University, Wellington Road, Clayton 3800, Victoria (Australia); Junk, Peter C. [School of Chemistry, Centre for Green Chemistry, Monash University, Wellington Road, Clayton 3800, Victoria (Australia); Forsyth, Maria [School of Physics and Materials Engineering, Centre for Green Chemistry, Monash University, Wellington Road, Clayton 3800, Victoria (Australia)]. E-mail: maria.forsyth@spme.monash.edu.au

    2006-02-15

    The corrosion inhibition mechanisms of new cerium and lanthanum cinnamate based compounds have been investigated through the surface characterisation of the steel exposed to NaCl solution of neutral pH. Attenuated Total Reflectance-Fourier Transform Infrared (ATR-FTIR) spectroscopy was used to identify the nature of the deposits on the metal surface and demonstrated that after accelerated tests the corrosion product commonly observed on steel (i.e. lepidocrocite, {gamma}-FeOOH) is absent. The cinnamate species were clearly present on the steel surface upon exposure to NaCl solution for short periods and appeared to coordinate through the iron. At longer times the Rare Earth Metal (REM) oxyhydroxide species are proposed to form as identified through the bands in the 1400-1500 cm{sup -1} region. These latter bands have been previously assigned to carbonate species adsorbed onto REM oxyhydroxide surfaces. The protection mechanism appears to involve the adsorption of the REM-cinnamate complex followed by the hydrolysis of the REM to form a barrier oxide on the steel surface.

  2. The nature of the surface film on steel treated with cerium and lanthanum cinnamate based corrosion inhibitors

    International Nuclear Information System (INIS)

    The corrosion inhibition mechanisms of new cerium and lanthanum cinnamate based compounds have been investigated through the surface characterisation of the steel exposed to NaCl solution of neutral pH. Attenuated Total Reflectance-Fourier Transform Infrared (ATR-FTIR) spectroscopy was used to identify the nature of the deposits on the metal surface and demonstrated that after accelerated tests the corrosion product commonly observed on steel (i.e. lepidocrocite, γ-FeOOH) is absent. The cinnamate species were clearly present on the steel surface upon exposure to NaCl solution for short periods and appeared to coordinate through the iron. At longer times the Rare Earth Metal (REM) oxyhydroxide species are proposed to form as identified through the bands in the 1400-1500 cm-1 region. These latter bands have been previously assigned to carbonate species adsorbed onto REM oxyhydroxide surfaces. The protection mechanism appears to involve the adsorption of the REM-cinnamate complex followed by the hydrolysis of the REM to form a barrier oxide on the steel surface

  3. Effect of cerium conversion of A3xx.x/SiCp composites surfaces on salt fog corrosion behaviour

    Energy Technology Data Exchange (ETDEWEB)

    Pardo, A.; Merino, M.C.; Arrabal, R.; Viejo, F.; Carboneras, M.; Coy, A.E. [Departamento de Ciencia de Materiales, Facultad de Quimica, Universidad Complutense, 28040, Madrid (Spain); Merino, S. [Departamento de Tecnologia Industrial, Universidad Alfonso X El Sabio, 28691, Villanueva de la Canada, Madrid (Spain)

    2004-07-01

    A study of the effect of cerium conversion treatment on surface of four composites (A360/SiC/10p, A360/SiC/20p, A380/SiC/10p, A380/SiC/20p) on their salt fog corrosion behaviour was performed. The conversion treatment was carried out using thermal activated full immersion in Ce(III) aqueous solutions. The matrix of A360/SiC/xxp composites is virtually free of Cu while the A380/SiC/xxp matrix contains 1.39-1.44 wt.%Ni and 3.13-3.45 wt.%Cu. Conversion performance was evaluated in neutral salt fog environment according to ASTM B117. The kinetics of the corrosion process were studied on the basis of gravimetric tests. The influence of SiCp proportion and matrix composition was evaluated and the nature of corrosion products was analysed by SEM and low angle XRD before and after accelerated testing to determine the influence of microstructural changes on corrosion behaviour during exposure to the corrosive environment. The Ce(III) precipitates on the cathodic sites, mainly on the intermetallic compounds, decreased both the cathodic current density and the corrosion rate of the composites tested. The presence of Cu in the matrix composition increased the corrosion rate, due to the galvanic couple Al/Cu. (authors)

  4. Band structure, cohesive properties, and Compton profile of γ- and α-cerium

    Science.gov (United States)

    Podloucky, R.; Glötzel, D.

    1983-03-01

    Recent Compton scattering experiments on the high-volume (γ) and low-volume (α) phases of fcc cerium and their interpretation in terms of the renormalized-free-atom model cast severe doubts on the promotional model of Pauling and Zachariasen for the γ-α transition. Stimulated by these results, we have extended a previous self-consistent local-density band-structure investigation to study the Compton profiles of γ- and α-cerium. For the band structure, Bloch functions, and their Fourier transforms we use the linear muffin-tin orbital method in the atomic-sphere approximation. We analyze the calculated Compton profiles in terms of band structure and local angular momentum character of the wave functions. The change in band structure and wave functions under compression (with approximately one electron per atom in the 4f band of both phases) accounts well for the observed change in the Compton profile. This provides further evidence against the promotional model in agreement with the analysis of Kornstädt et al. In addition, we study the cohesive energy of fcc cerium as a function of volume in the local-density approximation. For α-cerium in the 4f1(5d 6s)3 configuration we find a cohesive energy of 5.4 eV/atom in good agreement with experiment, whereas the "promotional" 4f0(5d 6s)4 state yields a binding energy of 0.6 eV/atom only. Therefore the fourth valence electron has to be a 4f electron, and α-cerium has to be regarded as an f-band metal.

  5. High temperature condensation and thermal radiation properties of cerium dioxide in solid and liquid states

    International Nuclear Information System (INIS)

    Full Text: Measuring thermal radiation properties of cerium dioxide at high temperatures is very complicated problem from experimental point of view. It is connected with high evaporation of this material at high temperatures. In order to solve this problem with a subsecond laser technique the excess pressure of inert atmosphere is maintained in the working chamber to suppress surface evaporation in the focal area of the sample. In this paper it is shown that in this case the dense vapor phase formed above the investigated sample actively interacts with the sample surface and the laser radiation and distorts the experimental results. The developed polychromatic reflectometer with laser heating enabled one to discover the interesting phenomenon of the interaction of the vapor, liquid and solid phases in cerium dioxide under CO2 laser irradiation. This phenomenon is exhibited in the form of the exothermic peak of the condensation on the cooling curves moreover the temperature level of this transition is regulated by experimental parameters. The possibility of the change of the position of this floating phase transition on the temperature scale permits one to model the interaction of liquid-vapor and solid-vapor to estimate the contribution of the dense vapor phase formed above the sample to the thermal radiation properties of cerium dioxide at high temperatures. The experimental data on thermal radiation properties of stoichiometric cerium dioxide in the spectral range 0.4-1.1 μm and in the temperature region 2000-3500 K measured by the method developed are presented. Reflectivity and emissivity measurement error does not exceed ±3 %. The experimental results obtained are compared with the data of other authors and the recommended values for spectral reflectivity and emissivity of cerium dioxide at high temperatures are given. (author)

  6. The importance of cerium substituted phosphates as cation exchanger some unique properties and related application potentials

    International Nuclear Information System (INIS)

    Seven different samples of an inorganic ion exchanger, cerium phosphate, suitable for column use have been prepared under varying conditions. The property of these exchangers has been characterized by Inductively Coupled Plasma Spectroscopy. These exchangers are stable in water, dilute mineral acids, ethanol, methanol, acetone and ether. However, in concentrated HCl and HNO3 they decompose. They retain about 50% of their exchange value after drying at 80 degC, and can be regenerated twice without any decrease in exchange capacity. The distribution coefficient measurements for alkaline earth metals, tellurium, iodine and molybdenum using these seven ion exchangers were studied. This revealed the relative affinity for each exchanger, where the sorption in general was most effective at P H 6-8. The titration curves of cerium phosphate (disodium) with alkaline earth metals showed that the selectivity sequence Ba2+>Sr2+>CA2+>Mg2+ is observed. Furthermore, it could be deduced that the adsorption of alkaline earth metal cations greatly depends on the cation. These studies have also shown that cerium phosphates with divalent ions are strongly preferred to monovalent ones. Therefore, as for the cerium phosphates with large monovalent ions, the lack of exchange for Ba2+, Mg2+ or other alkaline earth metal ions should be essentially due to steric hindrance and this could include any one of the following: the large crystalline radius of metal ions or large hydrated ionic radius and high energy of hydration for other divalent ions. Three binary separations of TeIV - MoIV, TeIV -I1 has been developed and the recovery ranging from 90 to 100% has been achieved on cerium phosphate (disodium) columns

  7. Using cerium anomaly as an indicator of redox reactions in constructed wetland

    Science.gov (United States)

    Liang, R.

    2013-12-01

    The study area, Chiayi County located in southern Taiwan, has highly developed livestock. The surface water has very low dissolved oxygen and high NH4. Under the situation, constructed wetland becomes the most effective and economic choice to treat the wastewater in the natural waterways. Hebao Island free surface constructed wetland started to operate in late 2006. It covers an area of 0.28 km2 and is subdivided into 3 major cells, which are sedimentation cell, 1st aeration cell with rooted plants and 2nd aeration cell with float plants. The water depth of cells ranges from 0.6 m to 1.2 m. The total hydraulic retention time is about a half day. In this study, the water samples were sequentially collected along the flow path. The results of hydrochemical analysis show that the untreated inflow water can be characterized with enriched NH4 (11 ppm), sulfate (6 ppm) and arsenic (50 ppb). The removal efficiency of NH4 in the first two cells is pollutants from the wastewater; therefore, dissolved oxygen is traditionally considered as an important indicator to evaluate the operation efficiency of wetland. However, it would need longer time to achieve equilibrium state of redox reaction involving dissolved oxygen due to the slower reaction rate. For example, the input water in this study has fairly high dissolved oxygen (5 ppm) but the NH4 content is still high, which indicates a non-equilibrium condition. In this study, the cerium anomaly is alternatively utilized to evaluate the water redox state. The results demonstrate that the input water has the negative cerium anomaly of -0.16. Along the flow path, the cerium negative anomaly does not change in the first two cells and dramatically becomes -0.23 in cell 3. The trend of cerium anomaly is more close to the removal efficiency of NH4 rather than dissolve oxygen. Accordingly, cerium anomaly could become a better indicator of removal efficiency of constructed wetland.

  8. Electron spectroscopy study of the heavy fermion compounds URu2Si2

    International Nuclear Information System (INIS)

    We report x-ray photoemission, resonant photoemission and bremsstrahlung isochromat spectra of the 4f core levels, the valence band and the conduction band, respectively, of the heavy fermion compounds URu2Si2. The resonant photoemission behavior of the uranium 5f weight resembles that of cerium 4f weight in that the portion away from the Fermi energy has a delayed resonance relative to that at the Fermi energy. We also assess current efforts to interpret uranium spectra. (author)

  9. Equation of state measurements by radiography provide evidence for a liquid-liquid phase transition in cerium

    Science.gov (United States)

    Lipp, M. J.; Jenei, Zs; Ruddle, D.; Aracne-Ruddle, C.; Cynn, H.; Evans, W. J.; Kono, Y.; Kenney-Benson, C.; Park, C.

    2014-05-01

    A pressure-volume isotherm in cerium metal at 1100 K was measured in a large volume press of the Paris-Edinburgh type up to 6 GPa. The volume was determined by imaging a rectangular shape of the sample via white X-ray radiography. Energy dispersive x-ray diffraction spectra were recorded to ensure that the highly reactive cerium in the cell assembly remained pure at this temperature. Even at 1100 K the p-V equation of state of liquid cerium shows a pronounced decrease of the bulk modulus above the y-phase region similar to the 775 K isotherm in the solid that also shows an inflection point between y- and a-type cerium. The inflection point in the 1100 K isotherm indicating the minimum in the bulk modulus separating the γ- from the α-type liquid is located at approximately 3.5 GPa.

  10. Effect of HCl pre-treatment on corrosion resistance of cerium-based conversion coatings on magnesium and magnesium alloys

    Energy Technology Data Exchange (ETDEWEB)

    Brunelli, Katya [Department of Mechanical Innovation and Management, University of Padua, Via Marzolo 9, 35131 Padua (Italy); Dabala, Manuele [Department of Mechanical Innovation and Management, University of Padua, Via Marzolo 9, 35131 Padua (Italy)]. E-mail: manuele.dabala@unipd.it; Calliari, Irene [Department of Mechanical Innovation and Management, University of Padua, Via Marzolo 9, 35131 Padua (Italy); Magrini, Maurizio [Department of Mechanical Innovation and Management, University of Padua, Via Marzolo 9, 35131 Padua (Italy)

    2005-04-01

    The corrosion protection afforded by a cerium conversion coating, formed by immersion in a solution containing rare earth salt and hydrogen peroxide, on pure magnesium and two magnesium alloys, AZ91 and AM50, has been studied. The effect of HCl pre-treatments on the morphology and on the corrosion resistance of the cerium conversion layer was investigated. A thicker and more homogeneous distribution of the conversion coating was obtained when the sample surface was pre-treated with acid. Higher amounts of cerium on the surface of the pre-treated samples were detected. The cerium conversion coating increased the corrosion resistance of the alloys because it ennobled the corrosion potential and decreased both the anodic and cathodic current. The acid pre-treatment further increased the corrosion resistance of the coated alloys. After five days of immersion in chloride environment the untreated samples showed localized corrosion while the chemical conversion coated samples appeared unaffected.

  11. Titrimetric and Spectrophotometric Assay of Ganciclovir in Pharmaceuticals Using Cerium(IV) Sulphate as the Oxidimetric Agent

    OpenAIRE

    Pavagada J. Ramesh; Kanakapura Basavaiah; Cijo M. Xavier; Prashanth, Kudige N.; Raghu, Madihalli S.; Kanakapura B. Vinay

    2012-01-01

    Titrimetric and spectrophotometric assay of ganciclovir (GNC) is described using cerium(IV) sulphate as the oxidimetric reagent. The methods are based on the oxidation of GNC with a measured excess of cerium(IV) sulphate in acid medium followed by determination of the unreacted oxidant by two different reaction schemes. In titrimetry, the unreacted oxidant was determined by back titration with ferrous ammonium sulphate (FAS) in sulphuric acid medium, and spectrophotometry involves the reactio...

  12. Reactions between cerium(IV) and methyl-6-x-derivatives of aniline in perchloric acid solutions

    International Nuclear Information System (INIS)

    The oxidation of 2,6-dimethyl-, 2-isopropyl-6-methyl, 2-chloro-6-methyl-and 2-methyl-6-nitro aniline with cerium(IV) in perchloric acid solutions has been examined. It has been found that the concentration of hydrogen ions and the basicity of nitrogen atom in the amine group decide about the resultant intermediate products. Some of these products can be practically prepared using cerium(IV) as an oxidizing agent. (author). 16 refs, 1 tab

  13. The dissolution and formation enthalpy of alloys and intermetallics of aluminium-lanthanum and aluminium-cerium systems

    International Nuclear Information System (INIS)

    Present article is devoted to dissolution and formation enthalpy of alloys and intermetallics of aluminium-lanthanum and aluminium-cerium systems. Therefore the dissolution temperatures of alloys and intermetallics of aluminium-lanthanum and aluminium-cerium systems were defined by means of calorimetry method. The enthalpy of formation of intermetallics of Al-Ce system was defined as well. The regularities in changes of dissolution and formation enthalpy of alloys and intermetallics depending on composition were studied.

  14. Chromatographic separation of cerium(Ⅲ) in L-valine medium using poly[dibenzo-18-crown-6

    Institute of Scientific and Technical Information of China (English)

    SABALE Sandip R; MOHITE Baburao S

    2009-01-01

    A column chromatographic method has been developed for the separation and determination of cerium(Ⅲ) using poly[dibenzo-18-crown-6]. The separation was carried out in L-valine medium. The adsorption of cerium(Ⅲ) was quantitative from 1×10-1 to 1×10-4 mol/L L-valine. Amongst the various eluents, 1.0-8.0 mol/L hydrochloric acid, 1.0-8.0 mol/L hydrobromic acid, 1.0-8.0 mol/L perchloric acid, 1.0-2.0 mol/L sulfuric acid and 4.0-5.0 mol/L acetic acid, were found to be the efficient eluents for cerium(Ⅲ). The capacity of poly[dibenzo-18-crown-6] for cerium(Ⅲ) was (0.428±0.01) mmol/g. The method was applied to the separation of cerium(Ⅲ) from associated elements link uranium(Ⅵ) and thorium(Ⅳ). It was also applied for the determination of cerium(Ⅲ) in geological samples. The method is simple, rapid and selective with good reproducibility (approximately±2% ).

  15. Thermodynamic studies in the system cerium-gadolinium-oxygen. Thermodynamische Untersuchungen am System Cer-Gadolinium-Sauerstoff; Kalorimetrische und elektrochemische Methoden

    Energy Technology Data Exchange (ETDEWEB)

    Stelzer, N.

    1993-01-01

    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 Gd[sub 2]O[sub 3]. 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)

  16. Recovery of Cerium Dioxide from Spent Glass-Polishing Slurry and Its Utilization as a Reactive Sorbent for Fast Degradation of Toxic Organophosphates

    OpenAIRE

    Pavel Janoš; Pavel Kuráň; Jakub Ederer; Martin Šťastný; Luboš Vrtoch; Martin Pšenička; Jiří Henych; Karel Mazanec; Miroslav Skoumal

    2015-01-01

    The recovery of cerium (and possibly other rare earth elements) from the spent glass-polishing slurries is rather difficult because of a high resistance of polishing-grade cerium oxide toward common digestion agents. It was shown that cerium may be extracted from the spent polishing slurries by leaching with strong mineral acids in the presence of reducing agents; the solution may be used directly for the preparation of a ceria-based reactive sorbent. A mixture of concentrated nitric acid and...

  17. Synthesis of mesoporous cerium-zirconium mixed oxides by hydrothermal templating method

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    Mesoporous cerium-zirconium mixed oxides were prepared by hydrothermal method using cetyl trimethyl ammonium bromide (CTAB) as template.The effects of amount of template,pH value of solution and hydrothermal temperature on mesostructure of samples were systematically investigated.The final products were characterized by XRD,TEM,FT-IR,and BET.The results indicate that all the cerium-zirconium mixed oxides present a meso-structure.At molar ratio of n(CTAB)/n((Ce)+(Zr))=0.15,pH value of 9,and hydrothermal temperature of 120 ℃,the samples obtained possess a specific surface area of 207.9 m2/g with pore diameter of 3.70 nm and pore volume of 0.19 cm3/g.

  18. Radioluminescence and phosphororescence in electron-tube glasses doped with tin and cerium oxides

    International Nuclear Information System (INIS)

    Cerium and tin additions effect upon radioluminescence and phosphorescence of glasses (basic components are: SiO2, Al2O-3, ZnO, B2O3, Na2O, K2O) exposed to gamma radiation is studied. It has been shown that the following small amounts of CeO2 and SnO2 additions cause a considerable change in radioluminescence (2 times) and phosphorescence (more than an order). Tin oxide concentration increase results in radioluminescence growth in the short-wave spectral region. The dependence of radioluminescence and phosphorescence on cerium oxide concentration as well as the dependence of phosphorescence on tin oxide concentration has its maximum at 0.5-0.7 mass% of these additions. Radiation and optical characteristics of the glass under study have been compared to those of industrial glasses

  19. Growth of monodisperse nanocrystals of cerium oxide during synthesis and annealing

    International Nuclear Information System (INIS)

    Monodisperse cerium oxide nanocrystals have been successfully synthesised using simple ammonia precipitation technique from cerium(III) nitrate solution at different temperatures in the range 35-80 oC. The activation energy for growth of CeO2 nanocrystals during the precipitation is calculated as 11.54 kJ/mol using Arrhenius plot. Average crystal diameter was obtained from XRD analysis, HR-TEM and light scattering (PCS). The analysis of size data from HR-TEM images and PCS clearly indicated the formation of highly crystalline CeO2 particles in narrow size range. CeO2 nanocrystals precipitated at 35 oC were further annealed at temperatures in the range 300-700 oC. The activation energy for crystal growth during annealing is also calculated and is close to the reported values. An effort is made to predict the mechanism of crystal growth during the precipitation and annealing.

  20. Improvement and analysis of the hydrogen-cerium redox flow cell

    Science.gov (United States)

    Tucker, Michael C.; Weiss, Alexandra; Weber, Adam Z.

    2016-09-01

    The H2-Ce redox flow cell is optimized using commercially-available cell materials. Cell performance is found to be sensitive to the upper charge cutoff voltage, membrane boiling pretreatment, methanesulfonic-acid concentration, (+) electrode surface area and flow pattern, and operating temperature. Performance is relatively insensitive to membrane thickness, Cerium concentration, and all features of the (-) electrode including hydrogen flow. Cell performance appears to be limited by mass transport and kinetics in the cerium (+) electrode. Maximum discharge power of 895 mW cm-2 was observed at 60 °C; an energy efficiency of 90% was achieved at 50 °C. The H2-Ce cell is promising for energy storage assuming one can optimize Ce reaction kinetics and electrolyte.

  1. Color-Fading Spectrophotometric Determination of Cerium with DBC-Arsenazo

    Institute of Scientific and Technical Information of China (English)

    翟庆洲; 张晓霞

    2004-01-01

    In the medium of 0.18~1.08 mol·L-1 sulfuric acid, cerium(Ⅳ) has the color-fading effect on DBC-arsenazo. The apparent molar absorptivity of the color-fading reaction is ε530 nm=1.03×104 L·mol-1·cm-1. Beer′s law is obeyed over the range of 1.20~12.0 μg·ml-1 of Ce (Ⅳ) which shows a linear relationship with the decrease in the absorbance of the colored solution. The effect of thirty-six coexisting ions was studied. The method was applied to the determination of the trace amount of cerium in water samples and has the advantage of high accuracy and good selectivity.

  2. Monte Carlo radiative transfer simulation of a cavity solar reactor for the reduction of cerium oxide

    Energy Technology Data Exchange (ETDEWEB)

    Villafan-Vidales, H.I.; Arancibia-Bulnes, C.A.; Dehesa-Carrasco, U. [Centro de Investigacion en Energia, Universidad Nacional Autonoma de Mexico, Privada Xochicalco s/n, Col. Centro, A.P. 34, Temixco, Morelos 62580 (Mexico); Romero-Paredes, H. [Departamento de Ingenieria de Procesos e Hidraulica, Universidad Autonoma Metropolitana-Iztapalapa, Av. San Rafael Atlixco No.186, Col. Vicentina, A.P. 55-534, Mexico D.F 09340 (Mexico)

    2009-01-15

    Radiative heat transfer in a solar thermochemical reactor for the thermal reduction of cerium oxide is simulated with the Monte Carlo method. The directional characteristics and the power distribution of the concentrated solar radiation that enters the cavity is obtained by carrying out a Monte Carlo ray tracing of a paraboloidal concentrator. It is considered that the reactor contains a gas/particle suspension directly exposed to concentrated solar radiation. The suspension is treated as a non-isothermal, non-gray, absorbing, emitting, and anisotropically scattering medium. The transport coefficients of the particles are obtained from Mie-scattering theory by using the optical properties of cerium oxide. From the simulations, the aperture radius and the particle concentration were optimized to match the characteristics of the considered concentrator. (author)

  3. Effect of cerium oxide addition on electrical and physical properties of alkali borosilicate glasses

    International Nuclear Information System (INIS)

    The study of electrical conductivity, density and coefficient of thermal expansion (CTE) of Na2O:K2O:B2O3:SiO2:BaO glass samples with addition of cerium oxide has been carried out. It has been observed that the addition of cerium oxide affects the electrical conductivity, density and CTE. The results have been explained on the basis of the variation in number of bridging oxygens (BOs) and non-bridging oxygens (NBOs) present in the glass. In general, the glass with more NBOs has a weak network which exhibits higher electrical conductivity. The weakening of the network has been supported by the observed decrease in density and increase in CTE for the glasses.

  4. Spectral tunability of cerium photoluminescence in nano sized LaF3:Ce3+

    International Nuclear Information System (INIS)

    Nano sized LaF3:Ce3+ was synthesized by adopting co-precipitation technique with nominal composition as well as with different molar ratio of reactants La3+ (Lanthanum) and F− (Fluoride). All the samples were subjected to X-ray diffraction (XRD), XRF, UV-Vis absorption, and PL characterizations. XRD analysis did not reveal any significant change in the diffraction profile. Particle size variations were observed with respect to change in lanthanum to fluoride molar ratio. An interesting and intense photoluminescence excitation peaks were observed for the samples prepared non-stoichiometrically. The effect of varying nominal reactant composition demonstrates a possibility of introducing tunability in cerium emission in the same host. Life time of cerium has been measured to be in the order of nano seconds

  5. Energy transfer and thermal studies of Pr3+ doped cerium oxalate crystals

    Indian Academy of Sciences (India)

    R Pragash; Gijo Jose; N V Unnikrishnan; C Sudarsanakumar

    2011-07-01

    Energy transfer process at room temperature for cerium (sensitizer) oxalate single crystals doped with different concentrations (10, 13, 15, 17 and 20%) of praseodymium ions (activator) grown by hydro silica gel method has been evaluated. The analysis of energy level diagrams of cerium and praseodymium ions indicates that the energy gap between the sensitizer and the activator ions varies in a small range suggesting a possible energy transfer from the Ce3+ to Pr3+. The emission and absorption spectra of these crystals were recorded. The overlapping of the absorption spectra of Pr3+ and emission spectra of Ce3+ at wavelengths 484 and 478 nm, respectively, strongly supports the possible energy transfer process in this system. From the absorption spectra, oscillator strength, electric dipole moment, branching ratio and Judd–Ofelt parameters of this system were evaluated by least square programming. The quantum efficiency, energy transfer probabilities and thermal properties have been studied.

  6. Effect of cerium addition on microstructure and texture of aluminum foil for electrolytic capacitors

    Institute of Scientific and Technical Information of China (English)

    王海燕; 李文学; 任慧平; 黄丽颖; 王向阳

    2010-01-01

    Anode foil of aluminum electrolytic capacitor,which requires large surface area for high capacitance,were prepared by rolling,annealing and electrochemical etching.Effects of cerium addition on the capacitance of aluminum electrolytic capacitors were investigated.Microstructure of the aluminum foil surface was observed by optical microscopy(OM) and scanning electron microscopy(SEM).Electron back scattered diffraction(EBSD) was also employed to reveal texture evolvement of cold-rolled aluminum foil after ann...

  7. Protection of the AZ31 magnesium alloy with cerium modified silane coatings

    International Nuclear Information System (INIS)

    Highlights: → Silane conversion coatings as possible alternative to Cr(VI) based pre-treatments. → 3-mercapto-propyl-trimethoxysilane (PropS-SH) tested on Mg alloys. → PropS-SH forms a porous conversion coating which allows a rapid electrolyte uptake. → Ce(NO3)3 addition to pre-treatment bath improves PropS-SH coating performance. → Ce3+ ions presence provides self-healing feature to the coating. - Abstract: This research investigates the effect of cerium ion addition on the efficiency of a 3-mercapto-propyl-trimethoxysilane (PropS-SH) coating formed on AZ31 magnesium alloy. The coating was obtained by dipping AZ31 coupons in a hydroalcoholic 3-mercapto-propyl-trimethoxysilane solution, added with cerium nitrate, in order to obtain a 5 x 10-3 or 5 x 10-4 M Ce+3 ion concentration. The silane baths were regulated at pH 4 and utilized for filming treatment after 48 h following their preparation. The treated specimens were finally cured for 1 h at 100 deg. C. The protective efficiency of cerium modified and unmodified PropS-SH coatings was evaluated by recording potentiodynamic polarization curves and electrochemical impedance spectra in a 0.1 M NaCl environment. In comparison to PropS-SH coating, cerium nitrate modified silane layer exhibited noticeably improved performances, in particular in presence of a 5 x 10-3 M Ce3+ concentration. The increased protectiveness and stability of the modified coatings were attributed to a lower porosity and defectiveness and to self-healing ability provided by Ce3+ ion presence.

  8. Theoretical modeling of heterogeneous catalysts based on platinum and cerium oxide

    OpenAIRE

    Bruix Fusté, Albert

    2014-01-01

    This thesis focuses on the computational study of models for platinum catalysts supported on cerium oxide (CeO2) which are of technological relevance. In these catalysts, ceria is often found acting as a non-inert support, leading to complex metal-support interactions (MSI) that modify the properties of both the oxide and the supported metal. First principles computational methods based on the Density functional Theory (DFT) have been used to study the nature of these interactions and their e...

  9. A cerium glass fiber-optic active target for high energy physics experiments

    International Nuclear Information System (INIS)

    A fiber-optic plate imaging system has been developed for active target and tracking applications, in which the active element is Ce(3+) in a silicate glass. Particle tracks and interactions have been recorded with a hit density of greater than or equal to 4/mm for minimum ionizing particles and with a spatial resolution sigma approx. = 28μ m.) The properties of cerium scintillation glass are discussed

  10. Redox-active cerium oxide nanoparticles protect human dermal fibroblasts from PQ-induced damage

    OpenAIRE

    Claudia von Montfort; Lirija Alili; Sarah Teuber-Hanselmann; Peter Brenneisen

    2014-01-01

    Recently, it has been published that cerium (Ce) oxide nanoparticles (CNP; nanoceria) are able to downregulate tumor invasion in cancer cell lines. Redox-active CNP exhibit both selective pro-oxidative and antioxidative properties, the first being responsible for impairment of tumor growth and invasion. A non-toxic and even protective effect of CNP in human dermal fibroblasts (HDF) has already been observed. However, the effect on important parameters such as cell death, proliferation and red...

  11. Nanocrystalline cerium dioxide efficacy for gastrointestinal motility: potential for prokinetic treatment and prevention in elderly

    OpenAIRE

    Yefimenko, Olena Yu; Savchenko, Yuliya O; Tetyana M. Falalyeyeva; Beregova, Tetyana V; Zholobak, Nadiya M; Spivak, Mykola Ya; Shcherbakov, Oleksandr B; Bubnov, Rostyslav V

    2015-01-01

    Background Constipation is a common condition, with prevalence after 65 years, is a major colorectal cancer risk factor. Recent works have demonstrated advances in personalized, preventive nanomedicine, leading to the construction of new materials and nanodrugs, in particular, nanocrystalline cerium dioxide (NCD), having strong antioxidative prebiotic effect. The aim of our study was to investigate the influence of NCD on motor function of the stomach and colon in vivo and contractive activit...

  12. Untangling the biological effects of cerium oxide nanoparticles: the role of surface valence states

    OpenAIRE

    Gerardo Pulido-Reyes; Ismael Rodea-Palomares; Soumen Das; Tamil Selvan Sakthivel; Francisco Leganes; Roberto Rosal; Sudipta Seal; Francisca Fernández-Piñas

    2015-01-01

    Cerium oxide nanoparticles (nanoceria; CNPs) have been found to have both pro-oxidant and anti-oxidant effects on different cell systems or organisms. In order to untangle the mechanisms which underlie the biological activity of nanoceria, we have studied the effect of five different CNPs on a model relevant aquatic microorganism. Neither shape, concentration, synthesis method, surface charge (ζ-potential), nor nominal size had any influence in the observed biological activity. The main drive...

  13. One step hydrothermal synthesis of a carbon nanotube/cerium oxide nanocomposite and its electrochemical properties

    Science.gov (United States)

    Kalubarme, Ramchandra S.; Kim, Yong-Han; Park, Chan-Jin

    2013-09-01

    A carbon nanotube (CNT)/cerium oxide composite was prepared by a one-pot hydrothermal reaction in the presence of KOH and capping agent polyvinylpyrrolidone. The nanocomposite displayed pronounced capacitive behaviour with very small diffusion resistance. The electrochemical performance of the composite electrode in a symmetric supercapacitor displayed a high energy density of 35.9 Wh kg-1 corresponding to a specific capacitance of 289 F g-1. These composite electrodes also demonstrated a long cycle life with better capacity retention.

  14. Cerium regulates expression of alternative methanol dehydrogenases in Methylosinus trichosporium OB3b.

    Science.gov (United States)

    Farhan Ul Haque, Muhammad; Kalidass, Bhagyalakshmi; Bandow, Nathan; Turpin, Erick A; DiSpirito, Alan A; Semrau, Jeremy D

    2015-11-01

    Methanotrophs have multiple methane monooxygenases that are well known to be regulated by copper, i.e., a "copper switch." At low copper/biomass ratios the soluble methane monooxygenase (sMMO) is expressed while expression and activity of the particulate methane monooxygenase (pMMO) increases with increasing availability of copper. In many methanotrophs there are also multiple methanol dehydrogenases (MeDHs), one based on Mxa and another based on Xox. Mxa-MeDH is known to have calcium in its active site, while Xox-MeDHs have been shown to have rare earth elements in their active site. We show here that the expression levels of Mxa-MeDH and Xox-MeDH in Methylosinus trichosporium OB3b significantly decreased and increased, respectively, when grown in the presence of cerium but the absence of copper compared to the absence of both metals. Expression of sMMO and pMMO was not affected. In the presence of copper, the effect of cerium on gene expression was less significant, i.e., expression of Mxa-MeDH in the presence of copper and cerium was slightly lower than in the presence of copper alone, but Xox-MeDH was again found to increase significantly. As expected, the addition of copper caused sMMO and pMMO expression levels to significantly decrease and increase, respectively, but the simultaneous addition of cerium had no discernible effect on MMO expression. As a result, it appears Mxa-MeDH can be uncoupled from methane oxidation by sMMO in M. trichosporium OB3b but not from pMMO. PMID:26296730

  15. Development of Stable Cerium Zirconium Mixed Oxide Nanoparticle Additive for Emission Reduction in Biodiesel Blends

    Directory of Open Access Journals (Sweden)

    Sajith V

    2015-06-01

    Full Text Available Harmful emissions associated with the use of biodiesel is a serious issue and various fuel additives are being used for the reduction of emissions as well as for the improvement of engine performance. Use of cerium oxide nanoparticles as fuel additive is one of the methods for the reduction of emissions, due to its peculiar redox functionality and oxygen buffering capability. Doping of ceria with transition metals such as zirconium improves its Oxygen storage capacity and thermal stability, thereby enhancing simultaneous oxidation and reduction reactions. The present work focuses on the development of cerium zirconium mixed oxide nanoparticle based additive for the reduction of emissions from diesel engine fuelled with biodiesel - diesel blends. Cerium zirconium mixed oxide was synthesized by means of co precipitation method. The stability of the nanofluids was improved by the addition of surfactant, namely Oleic acid. The optimum concentration of surfactant was determined based on estimation of critical micelle concentration, by means of standard tests. Stability of catalytic nanoparticle in fuel was evaluated from the measurement of Zeta potential. Various properties were determined as per ASTM standards to investigate the effect of the nanoparticles on fuel properties. Addition of catalytic nanoparticle in diesel - biodiesel blends does not significantly affect the fuel properties. Engine performance and emission tests were conducted on single cylinder diesel engine to assess the potential of synthesized nanofuel and 15% average reduction of NO emissions was observed for B5 and B10 blends with 15 ppm of catalytic nanoparticle concentration.

  16. The role of hydrogen peroxide in the deposition of cerium-based conversion coatings

    International Nuclear Information System (INIS)

    Cerium-based conversion coatings are progressing as an effective alternative to hazardous chromate-based systems used in the treatment of metal surfaces. However, there is still considerable debate over the mechanism by which these coatings are formed. Here, titrations of cerium-based conversion coating solutions were carried out in order to model the reactions that occur at the metal-solution interface during coating, with a particular emphasis on investigating the role of hydrogen peroxide (H2O2). The titration curves obtained support the proposed formation of Ce(III) peroxo complexes such as Ce(H2O2)3+ as an initial step, followed by deprotonation, oxidation and precipitation to form peroxo-containing Ce(IV) species such as Ce(IV)(O2)(OH)2. The precipitates resulting from titrations were characterised by Raman spectroscopy, X-ray diffraction and thermogravimetric analysis, confirming the presence of peroxo bonds, and nano-sized CeO2 crystallites that decreased in size with increasing H2O2 concentration. Characterisation of cerium conversion coatings on aluminium alloy surfaces confirmed the presence of peroxo species in the coatings, thereby supporting the titration model

  17. Cerium, gallium and zinc containing mesoporous bioactive glass coating deposited on titanium alloy

    Science.gov (United States)

    Shruti, S.; Andreatta, F.; Furlani, E.; Marin, E.; Maschio, S.; Fedrizzi, L.

    2016-08-01

    Surface modification is one of the methods for improving the performance of medical implants in biological environment. In this study, cerium, gallium and zinc substituted 80%SiO2-15%CaO-5%P2O5 mesoporous bioactive glass (MBG) in combination with polycaprolactone (PCL) were coated over Ti6Al4 V substrates by dip-coating method in order to obtain an inorganic-organic hybrid coating (MBG-PCL). Structural characterization was performed using XRD, nitrogen adsorption, SEM-EDXS, FTIR. The MBG-PCL coating uniformly covered the substrate with the thickness found to be more than 1 μm. Glass and polymer phases were detected in the coating along with the presence of biologically potent elements cerium, gallium and zinc. In addition, in vitro bioactivity was investigated by soaking the coated samples in simulated body fluid (SBF) for up to 30 days at 37 °C. The apatite-like layer was monitored by FTIR, SEM-EDXS and ICP measurements and it formed in all the samples within 15 days except zinc samples. In this way, an attempt was made to develop a new biomaterial with improved in vitro bioactive response due to bioactive glass coating and good mechanical strength of Ti6Al4 V alloy along with inherent biological properties of cerium, gallium and zinc.

  18. Microstructure and electrochemical behavior of cerium conversion coating modified with silane agent on magnesium substrates

    Science.gov (United States)

    Lei, Li; Shi, Jing; Wang, Xin; Liu, Dan; Xu, Haigang

    2016-07-01

    The cerium conversion coating with and without different concentrations of silane agent bis-(γ-triethoxysilylpropyl)-tetrasulfide (BTESPT) modification is obtained on magnesium alloys. Detailed properties of the coatings and the role of BTESPT as an additive are studied and followed with careful discussion. The coating morphology, wettability, chemical composition and corrosion resistance are characterized by scanning electronic microscope (SEM), water contact-angle, X-ray photoelectron spectroscopy (XPS), potentiodynamic measurements and electrochemical impedance spectroscopy (EIS). The electrochemical behavior of the coatings is investigated using EIS. The results indicate that the coating morphology and composition can be controlled by changing silane concentration. The combination of cerium ions and silane molecules could promote the formation of more homogenous and higher hydrophobic coating. The coating turns to be more compact and the adhesive strength between the coating and the magnesium substrate are strongly improved with the formation of Sisbnd Osbnd Si and Sisbnd Osbnd M chemical bonds. The optimum corrosion resistance of the coating in the corrosive media is obtained by 25 ml L-1 BTESPT modification. This whole study implies that the cerium conversion coating modified with certain silane agent deserves cautiousness before its application for corrosion resistance.

  19. Effect of cerium oxide addition on electrical properties of ZnO

    Energy Technology Data Exchange (ETDEWEB)

    Ibrahim, D.M. [National Research Center, Dokki, Giza (Egypt). Dept. of Ceramics; Mounir, M. [Dept. of Physics, Cairo Univ., Giza (Egypt); Mahgoub, A.S. [Cairo Univ., Giza (Egypt). Dept. of Chemistry; Turky, G. [Dept. of Physics, National Research Center, Dokki, Giza (Egypt); El-Desouky, O.A. [Cer. Cleopatra Co., Ramadan City (Egypt)

    2002-07-01

    Mixtures of ZnO and Ce{sub 6} O{sub 11} as additive were prepared by solid state reaction from the calcined oxides with the following proportions: 0.03, 0.08, 0.1, 0.2 and 0.4 mole. Disc specimens 1.2 cm 5 cm in diameter and 0.3 cm thickness were processed under a force of 70 kN and fired at 1150 C/ 30 minutes. XRD revealed the presence of limited solid solution of cerium in ZnO, as evident from the shift in the peaks [0.03-0.04 A ] up to 0.1 mole addition and remains constant. SEM revealed the presence of inter-granular phase. EDAX showed it to be a mixture of ZnO and Ce{sub 6}O{sub 11}. Also cerium was detected in the ZnO grains confirming the XRD results. RCL circuit was used to measure the capacitance and resistance at different frequencies at room temperature. The dielectric constant and conductivity were calculated. The change in resistivity with temperature was followed up to 523 K. The change in dielectric strength with temperature at spot frequency of 10 kHz is demonstrated. The electrical conductivity was found to increase with the proportion of cerium oxide up to 0.2 mole then decreased. (orig.)

  20. Laser ablated plasma plume diagnostics of cerium oxide: effect of oxygen partial pressure

    International Nuclear Information System (INIS)

    This paper describes the spatial and temporal investigation of laser ablated plasma plume of cerium oxide target using Langmuir probe to measure the plasma parameters. Cerium oxide target was ablated using a KrF (λ ∼ 248 nm) gas laser at an energy of 300 mJ per pulse. Experimental studies confirmed that oxygen partial pressure of 2 x 10-2 mbar is sufficient enough to get good quality films of cerium oxide. At this pressure, plume was diagnosed for their spatial and temporal behaviour. The tungsten probe tip was inserted along the length of the plasma to collect the ions and electrons effectively. A thin probe tip (about 0.4 mm diameter) was used to avoid plasma perturbation during measurements. A variable voltage was applied to the tip and corresponding current due to electrons and ions was collected. Spatial distribution was investigated at a regular interval of 15 mm from the target up maximum distance 45 mm and the temporal behaviour was recorded in the range of 0 to 50 μS with an interval of 0.5 μS. The ion and average electron density are found to be maximum at 30 mm from the target position and the plasma current of ceria is found to be maximum at 22 μS. (author)

  1. Cerium Modified Pillared Montmorillonite Supported Cobalt Catalysts for Fischer Tropsch Synthesis

    International Nuclear Information System (INIS)

    Fischer-Tropsch (FT) synthesis was accomplished over Al-pillared Montmorillonite supported 20 wt% Co modified with different weight% of cerium catalysts. These catalysts were prepared by impregnation method while structural characterizations of the prepared samples were performed by XRD, TPR, NH/sub 3/TPD, TGA, BET, XRF and SEM techniques. The Fischer Tropsch reaction was studied in fixed bed micro catalytic reactor at temperature range of 220, 260 and 275 degree C and at different pressure (1, 5 and 10 bars). From the activity results, it was found that by pillaring NaMMT with Al higher catalytic activity and lower methane selectivity of NaMMT was achieved. Furthermore, the results of FT synthesis reaction revealed that cerium incorporation increased the dispersion of Co/sub 3/O/sub 4/ on the surface and consequently resulted in enhanced catalytic activity. Additionally, the C/sub 5/-C/sub 12/ hydrocarbons and methane selectivity increased while C/sub 22+/ hydrocarbons selectivity was decreased over cerium modified catalysts. Higher reaction temperature (>220 degree C) resulted in significant enhancement in CO conversion and methane selectivity. Though, increase in pressure from 1 to 10 bars eventually resulted in increase in C/sub 5+/ hydrocarbons and decrease in methane and C/sub 2/-C/sub 5/ hydrocarbons selectivity. (author)

  2. Thermal decomposition study of uranyl nitrate and cerium hydroxide in a spray dryer

    International Nuclear Information System (INIS)

    A study, in a spray dryer system based on drying and thermal decomposition of uranyl nitrate solutions aiming the production of uranium trioxide adequate for the use in posterior steps of reduction and hydro fluorination in nuclear fuel cycle; and cerium hydroxide suspensions for the production of cerium oxide with high surface area is presented. Thus, the project and construction of a countercurrent spray dryer was elaborated for capacity of 10 Kg U O3/h and 3,5 k Ce O2/h. The methodology used in these experiments consisted in the analysis of several parameters (concentration and flow rate of the feed, atomization pressure and inlet temperature of the dryer) over the physical and chemical properties of the products. Using the obtained results, with the help of a mathematical model, it was developed the project of a continuous pilot unity for the production of uranium trioxide or cerium oxide, with capacity of 20 Kg U O3/h or 10 Kg Ce O2/h, respectively. (author)

  3. Basic study on decontamination of TRU waste with cerium-mediated electrolytic oxidation method

    International Nuclear Information System (INIS)

    It is important to decrease the radioactivity of transuranium (TRU) waste arising from reprocessing plants by the decontamination for its disposal. In order to dispose TRU waste safely and rationally, a decontamination technology is required to be developed. For this purpose, the Japan Atomic Energy Agency has conducted a basic study focusing on the cerium-mediated electrolytic oxidation (CeMEX) method. In this study, two series of tests were performed to confirm the sufficient corrosion rate for the decontamination of metallic waste with the CeMEX method. One is the pre-corrosion test to survey an optimum solution condition for the generation of cerium(IV) ion under different conditions in concentration of cerium(III) ion and nitric acid. The other is the corrosion test to evaluate the corrosion rate of stainless steel as simulating waste under the optimized solution condition. It was confirmed that the average corrosion rate of stainless steel was 3.3 μm/h for 90 hours. This means that the decontamination can be completed within 6 hours and that the decontamination solution can be recycled 15 times, assuming that the decontamination to the clearance-level needs corrosion depth of 20 μm. From the results, the CeMEX method is sufficiently applicable to the decontamination of TRU waste. (author)

  4. Cerium Biomagnification in a Terrestrial Food Chain: Influence of Particle Size and Growth Stage.

    Science.gov (United States)

    Majumdar, Sanghamitra; Trujillo-Reyes, Jesica; Hernandez-Viezcas, Jose A; White, Jason C; Peralta-Videa, Jose R; Gardea-Torresdey, Jorge L

    2016-07-01

    Mass-flow modeling of engineered nanomaterials (ENMs) indicates that a major fraction of released particles partition into soils and sediments. This has aggravated the risk of contaminating agricultural fields, potentially threatening associated food webs. To assess possible ENM trophic transfer, cerium accumulation from cerium oxide nanoparticles (nano-CeO2) and their bulk equivalent (bulk-CeO2) was investigated in producers and consumers from a terrestrial food chain. Kidney bean plants (Phaseolus vulgaris var. red hawk) grown in soil contaminated with 1000-2000 mg/kg nano-CeO2 or 1000 mg/kg bulk-CeO2 were presented to Mexican bean beetles (Epilachna varivestis), which were then consumed by spined soldier bugs (Podisus maculiventris). Cerium accumulation in plant and insects was independent of particle size. After 36 days of exposure to 1000 mg/kg nano- and bulk-CeO2, roots accumulated 26 and 19 μg/g Ce, respectively, and translocated 1.02 and 1.3 μg/g Ce, respectively, to shoots. The beetle larvae feeding on nano-CeO2 exposed leaves accumulated low levels of Ce since ∼98% of Ce was excreted in contrast to bulk-CeO2. However, in nano-CeO2 exposed adults, Ce in tissues was higher than Ce excreted. Additionally, Ce content in tissues was biomagnified by a factor of 5.3 from the plants to adult beetles and further to bugs. PMID:26690677

  5. Synthesis and Characterization of Cerium Doped Titanium Catalyst for the Degradation of Nitrobenzene Using Visible Light

    Directory of Open Access Journals (Sweden)

    Padmini Ellappan

    2014-01-01

    Full Text Available Cerium doped catalyst was synthesized using Titanium isopropoxide as the Titanium source. The metal doped nanoparticles semiconductor catalyst was prepared by sol-sol method with the sol of Cerium. The synthesized catalyst samples were characterized by powder X-ray diffraction, BET surface area, thermogravimetric analysis (TGA, scanning electron microscopy (SEM, and UV-vis diffuse reflectance measurements (DRS and compared with undoped TiO2 catalyst. The photocatalytic activity of the sample was investigated for the decomposition of nitrobenzene (NB using visible light as the artificial light source. Cerium doped catalyst was found to have better degradation of nitrobenzene owing to its shift in the band gap from UV to visible region as compared to undoped TiO2 catalyst. The operational parameters were optimized with catalyst dosage of 0.1 g L−1, pH of 9, and light intensity of 500 W. The degradation mechanism followed the Langmuir Hinshelwood kinetic model with the rate constant depending nonlinearly on the operational parameters as given by the relationship Kapp (theoretical = 2.29 * 10−4 * Intensity0.584 * Concentration−0.230 * Dosage0.425 * pH0.336.

  6. Specifics of new phase crystal nucleation during isostructural γ↔α transformation in cerium

    International Nuclear Information System (INIS)

    Specifics of new phase nucleation and subsequent growth under γ-α-transformation in cerium near the surface of the sample is suggested. It is assumed that this specifics can effect mechanical behaviour of a laminar sample under transition at three-point bend. Measurement of deflection of cerium samples at the sensitivity of ∼ 10-6 m at three-point loading was carried out in the 4.2-300 K temperature range at p=10-4 GPa as well as in a chamber of high pressure (in the range of hydrostatic pressures up to 1.0 GPa at T=293 K). It is shown that the effects of change in the form experimentally discovered in the given paper and accompanying isostructural γ-α-transformation in cerium may be explained by the fact that crystal nucleation of γ- and α-phases differing by the volume takes place mainly from the surface of the sample and not in its volume

  7. Chromium VI adsorption on cerium oxide nanoparticles and morphology changes during the process

    International Nuclear Information System (INIS)

    In this study, suspended cerium oxide nanoparticles stabilized with hexamethylenetetramine were used for the removal of dissolved chromium VI in pure water. Several concentrations of adsorbent and adsorbate were tested, trying to cover a large range of possible real conditions. Results showed that the Freundlich isotherm represented well the adsorption equilibrium reached between nanoparticles and chromium, whereas adsorption kinetics could be modeled by a pseudo-second-order expression. The separation of chromium-cerium nanoparticles from the medium and the desorption of chromium using sodium hydroxide without cerium losses was obtained. Nanoparticles agglomeration and morphological changes during the adsorption-desorption process were observed by TEM. Another remarkable result obtained in this study is the low toxicity in the water treated by nanoparticles measured by the Microtox commercial method. These results can be used to propose this treatment sequence for a clean and simple removal of drinking water or wastewater re-use when a high toxicity heavy metal such as chromium VI is the responsible for water pollution.

  8. Cerium-based coating for enhancing the corrosion resistance of bio-degradable Mg implants

    International Nuclear Information System (INIS)

    Recently there has been interest in employing degradable metallic implants for internal fixation in bone fracture healing. The major purpose of using degradable implants is to avoid a second surgery for implant removal when bone healing has completed. However, the corrosion rate of Mg in vivo is too high. Thus increasing the corrosion resistance of Mg is the key problem to address in the development of degradable Mg implants. One possible route is by way of surface treatment, which would lower the corrosion rate at the initial phase of bone healing, the period during which the implant provides mechanical support for the broken bone. In the present study cerium oxide coating was prepared on pure Mg by cathodic deposition in cerium nitrate solution followed by hydrothermal treatment. The coated samples were characterized by SEM, EDS and XRD. The corrosion resistance in Hanks' solution (a simulated body fluid) was studied using polarization method and electrochemical impedance spectroscopy (EIS). The corrosion resistance of cerium oxide coated Mg in Hanks' solution at 37 deg. C and pH 7.4 was higher than that of bare Mg by about two orders of magnitude.

  9. Upconversion luminescence of cerium doped CoWO4 nanomaterials

    International Nuclear Information System (INIS)

    In this paper we report the bluish green upconversion intrinsic photoluminescence (PL) observed at room temperature (RT) 300 K for the nanorange (27–50 nm) Ce3+ doped and undoped CoWO4 powder samples sintered in air at 600°C. Excitation by Xenon lamp at 600 nm was done and the emission was observed between 400 nm and 550 nm. Co1−xCexWO4 [where x=0.00, 0.02, and 0.03] compounds were prepared by the solution based co-precipitation method and characterised by X-ray powder diffraction (XRD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The surface morphology of the compounds was examined by scanning electron microscopy (SEM) techniques. Optical absorption and photoluminescence behaviour of the compounds in the rigid matrix were studied. High emission intensity and easy preparation make these systems potential candidates for application as luminescent materials. - Highlights: ► Ce3+ doped CoWO4 nanosamples were prepared by the co-precipitation method. ► Characterised by XRD, TEM, SEM and XPS. ► Upconversion intrinsic luminescence observed for nanosamples. ► Mechanism for the upconverted emission is explained. ► No upconverted luminescence observed for bulk samples.

  10. Influence of agglomeration of cerium oxide nanoparticles and speciation of cerium(III) on short term effects to the green algae Chlamydomonas reinhardtii

    International Nuclear Information System (INIS)

    Highlights: • Phosphate-dispersed CeO2 NP did not affect photosynthetic yield in C. reinhardtii. • Agglomerated CeO2 NP slightly decreased photosynthetic yield. • Cerium(III) was shown to affect photosynthetic yield and intracellular ROS level. • Slight effects of CeO2 NP were caused by dissolved Ce3+ ions present in suspensions. • Wild type and cell wall free mutant of C. reinhardtii showed the same sensitivity. - Abstract: Cerium oxide nanoparticles (CeO2 NP) are increasingly used in industrial applications and may be released to the aquatic environment. The fate of CeO2 NP and effects on algae are largely unknown. In this study, the short term effects of CeO2 NP in two different agglomeration states on the green algae Chlamydomonas reinhardtii were examined. The role of dissolved cerium(III) on toxicity, its speciation and the dissolution of CeO2 NP were considered. The role of cell wall of C. reinhardtii as a barrier and its influence on the sensitivity to CeO2 NP and cerium(III) was evaluated by testing both, the wild type and the cell wall free mutant of C. reinhardtii. Characterization showed that CeO2 NP had a surface charge of ∼0 mV at physiological pH and agglomerated in exposure media. Phosphate stabilized CeO2 NP at pH 7.5 over 24 h. This effect was exploited to test CeO2 NP dispersed in phosphate with a mean size of 140 nm and agglomerated in absence of phosphate with a mean size of 2000 nm. The level of dissolved cerium(III) in CeO2 NP suspensions was very low and between 0.1 and 27 nM in all tested media. Exposure of C. reinhardtii to Ce(NO3)3 decreased the photosynthetic yield in a concentration dependent manner with EC50 of 7.5 ± 0.84 μM for wild type and EC50 of 6.3 ± 0.53 μM for the cell wall free mutant. The intracellular level of reactive oxygen species (ROS) increased upon exposure to Ce(NO3)3 with effective concentrations similar to those inhibiting photosynthesis. The agglomerated CeO2 NP caused a slight decrease of

  11. Influence of agglomeration of cerium oxide nanoparticles and speciation of cerium(III) on short term effects to the green algae Chlamydomonas reinhardtii

    Energy Technology Data Exchange (ETDEWEB)

    Röhder, Lena A. [Eawag, Swiss Federal Institute of Aquatic Science and Technology, Department of Environmental Toxicology, Dübendorf 8600 (Switzerland); ETH-Zurich, Institute of Biogeochemistry and Pollutant Dynamics, Zürich 8092 (Switzerland); Brandt, Tanja [Eawag, Swiss Federal Institute of Aquatic Science and Technology, Department of Environmental Toxicology, Dübendorf 8600 (Switzerland); Sigg, Laura [Eawag, Swiss Federal Institute of Aquatic Science and Technology, Department of Environmental Toxicology, Dübendorf 8600 (Switzerland); ETH-Zurich, Institute of Biogeochemistry and Pollutant Dynamics, Zürich 8092 (Switzerland); Behra, Renata, E-mail: Renata.behra@eawag.ch [Eawag, Swiss Federal Institute of Aquatic Science and Technology, Department of Environmental Toxicology, Dübendorf 8600 (Switzerland)

    2014-07-01

    Highlights: • Phosphate-dispersed CeO₂ NP did not affect photosynthetic yield in C. reinhardtii. • Agglomerated CeO₂ NP slightly decreased photosynthetic yield. • Cerium(III) was shown to affect photosynthetic yield and intracellular ROS level. • Slight effects of CeO₂ NP were caused by dissolved Ce³⁺ ions present in suspensions. • Wild type and cell wall free mutant of C. reinhardtii showed the same sensitivity. - Abstract: Cerium oxide nanoparticles (CeO₂ NP) are increasingly used in industrial applications and may be released to the aquatic environment. The fate of CeO₂ NP and effects on algae are largely unknown. In this study, the short term effects of CeO₂ NP in two different agglomeration states on the green algae Chlamydomonas reinhardtii were examined. The role of dissolved cerium(III) on toxicity, its speciation and the dissolution of CeO₂ NP were considered. The role of cell wall of C. reinhardtii as a barrier and its influence on the sensitivity to CeO₂ NP and cerium(III) was evaluated by testing both, the wild type and the cell wall free mutant of C. reinhardtii. Characterization showed that CeO₂ NP had a surface charge of ~0 mV at physiological pH and agglomerated in exposure media. Phosphate stabilized CeO₂ NP at pH 7.5 over 24 h. This effect was exploited to test CeO₂ NP dispersed in phosphate with a mean size of 140 nm and agglomerated in absence of phosphate with a mean size of 2000 nm. The level of dissolved cerium(III) in CeO₂ NP suspensions was very low and between 0.1 and 27 nM in all tested media. Exposure of C. reinhardtii to Ce(NO₃)₃ decreased the photosynthetic yield in a concentration dependent manner with EC₅₀ of 7.5 ± 0.84 μM for wild type and EC₅₀ of 6.3 ± 0.53 μM for the cell wall free mutant. The intracellular level of reactive oxygen species (ROS) increased upon exposure to Ce(NO₃)₃ with effective concentrations similar to those inhibiting photosynthesis. The agglomerated Ce

  12. Evaluation of mechanically treated cerium (IV) oxides as corrosion inhibitors for galvanized steel

    International Nuclear Information System (INIS)

    The use of cerium salts as corrosion inhibitors for hot dip galvanized steel has been object of a numerous studies in the last few years. The role of cerium ions as corrosion inhibitors was proved: cerium is able to block the cathodic sites of the metal, forming insoluble hydroxides and oxides on the zinc surface. This fact leads to a dramatic decrease of the cathodic current densities and, therefore, to a reduction the overall corrosion processes. On the other hand, the potential of cerium oxides as corrosion inhibitors was also proposed. However, the real effectiveness of this kind of anticorrosive pigments has not been clarified yet. In this work cerium (IV) oxides are considered as corrosion inhibitors for galvanized steel. The corrosion inhibition mechanism of mechanically treated (milled) CeO2 alone and in combination with milled SiO2 nanoparticles was investigated. For this purpose milled CeO2, CeO2 and SiO2 milled together and milled SiO2 particles were studied as corrosion inhibitors in water solution. Therefore, the different mechanically treated particles were dispersed in 0.1 M NaCl solution to test their effectiveness as corrosion inhibitors for galvanized steel. The galvanized steel was immersed in the different solutions and the corrosion inhibition efficiency of the different particles was measured by means of electrochemical techniques. For this purpose, electrochemical impedance spectroscopy (EIS) measurements were carried out, monitoring the evolution of the corrosion processes occurring at the metal surface with the immersion time in the solution. The effect of the different pigments was also investigated by carrying out anodic and cathodic polarization measurements. The polarization curves were acquired under conditions of varied pH. The experimental measurements suggest that the mechanical treatment performed on the SiO2 and CeO2 particles promote the formation of an effective corrosion pigment. The tests evidence also the beneficial effect of

  13. Some regularities of Ce(3) and Ce(4) stabilization in their compounds with β-diketones

    International Nuclear Information System (INIS)

    Adduct formation of cerium (3) and cerium (4) β-diketonates (acetylacetonate, benzoylacetonate, dibenzoylmethanate and thenoyltrifluoroacetonate) with oxygen- and nitrogen-donor ligands (Q-α, α'-dipyridyl, o-phenanthroline, trioctylphosphine oxide and triphenylphosphine oxide) is studied. The compounds obtained as a results of the reactions are studied by means of IR-spectroscopic, derivatographic and X-ray phase methods. It is concluded that composition and thermodynamic stability of adducts of Ce(3) tris-β-diketonates are determined by correlation of donor properties of the basis and additional ligand and stability of adducts to oxidation - as well as by their solubility. Introduction of the additional ligand to the system Ce(4)-β-diketones even in the presence of air oxygen stabilizes Ce(3) and destabilizes Ce(4)

  14. Polyacrylic acid-coated cerium oxide nanoparticles: An oxidase mimic applied for colorimetric assay to organophosphorus pesticides.

    Science.gov (United States)

    Zhang, Shi-Xiang; Xue, Shi-Fan; Deng, Jingjing; Zhang, Min; Shi, Guoyue; Zhou, Tianshu

    2016-11-15

    It is important and urgent to develop reliable and highly sensitive methods that can provide on-site and rapid detection of extensively used organophosphorus pesticides (OPs) for their neurotoxicity. In this study, we developed a novel colorimetric assay for the detection of OPs based on polyacrylic acid-coated cerium oxide nanoparticles (PAA-CeO2) as an oxidase mimic and OPs as inhibitors to suppress the activity of acetylcholinesterase (AChE). Firstly, highly dispersed PAA-CeO2 was prepared in aqueous solution, which could catalyze the oxidation of TMB to produce a color reaction from colorless to blue. And the enzyme of AChE was used to catalyze the substrate of acetylthiocholine (ATCh) to produce thiocholine (TCh). As a thiol-containing compound with reducibility, TCh can decrease the oxidation of TMB catalyzed by PAA-CeO2. Upon incubated with OPs, the enzymatic activity of AChE was inhibited to produce less TCh, resulting in more TMB catalytically oxidized by PAA-CeO2 to show an increasing blue color. The two representative OPs, dichlorvos and methyl-paraoxon, were tested using our proposed assay. The novel assay showed notable color change in a concentration-dependent manner, and as low as 8.62 ppb dichlorvos and 26.73 ppb methyl-paraoxon can be readily detected. Therefore, taking advantage of such oxidase-like activity of PAA-CeO2, our proposed colorimetric assay can potentially be a screening tool for the precise and rapid evaluation of the neurotoxicity of a wealth of OPs. PMID:27208478

  15. Preparation of magnetron sputtered thin cerium oxide films with a large surface on silicon substrates using carbonaceous interlayers.

    Science.gov (United States)

    Dubau, Martin; Lavková, Jaroslava; Khalakhan, Ivan; Haviar, Stanislav; Potin, Valerie; Matolín, Vladimír; Matolínová, Iva

    2014-01-22

    The study focuses on preparation of thin cerium oxide films with a porous structure prepared by rf magnetron sputtering on a silicon wafer substrate using amorphous carbon (a-C) and nitrogenated amorphous carbon films (CNx) as an interlayer. We show that the structure and morphology of the deposited layers depend on the oxygen concentration in working gas used for cerium oxide deposition. Considerable erosion of the carbonaceous interlayer accompanied by the formation of highly porous carbon/cerium oxide bilayer systems is reported. Etching of the carbon interlayer with oxygen species occurring simultaneously with cerium oxide film growth is considered to be the driving force for this effect resulting in the formation of nanostructured cerium oxide films with large surface. In this regard, results of oxygen plasma treatment of a-C and CNx films are presented. Gradual material erosion with increasing duration of plasma impact accompanied by modification of the surface roughness is reported for both types of films. The CNx films were found to be much less resistant to oxygen etching than the a-C film. PMID:24372305

  16. Effects of cerium microalloying on the structure and properties of heat resistant steel of 4Kh4VMFS

    International Nuclear Information System (INIS)

    It is attempted to follow the peculiarity of structural-physical changes under high-temperature heating in subcritical region and on this base possible mechanisms of cerium effect on heat resistance increase of instrumental compos ition (0.42% C; 0.80% Si; 0.37% Mn; 4.0% Cr; 0.98% W; 1.55% Mo; 1.22% V; 0.01% Ca including the variant with 0.08% Ce) is chosen for investigation. Cerium microalloying is shown to result in advisability of precipitations in the 400-500 deg C tempering temperature range of cementite carbides on the boundaries and in the centre of matrix grains that is associated with liquating inhomogeneity by cerium and carbon. The noted inhomogeneity is levelled with the increase of tempering temperature above 500 deg C. Cerium inhibits the process of Fesub(α)-solid solution decomposition under tempering and its depletion by tungsten and molybdenum. Cerium microalloying of 4Kh4VMFS steel restrains carbide phase coagulation at high temperatures of tempering, it promotes inhibiting the recrystallization processes, assures increased fracture toughness

  17. Effect of cerium additive and secondary phase analysis on Ag0.5Bi0.5TiO3 ceramics

    Indian Academy of Sciences (India)

    S Supriya; Antonio J Dos Santos-García; F Fernández-Martinez

    2016-02-01

    Cerium-doped silver bismuth titanate—Ag0.5Bi0.5TiO3 (ABT) ceramics have been synthesized by the high-temperature solid-state reaction method. The structure and elemental examination of the prepared ceramic was analysed by X-ray diffraction (XRD), Fourier transform infrared, scanning electron microscopy and energydispersive spectroscopy. XRD analysis showed the presence of pyrochlore structure and secondary phase when more than 5 mol% cerium was added. The impact of temperature on cerium-doped silver bismuth titanate samples was analysed by differential thermal analysis and differential scanning calorimetry. Cerium doping caused the flaky morphology comparing with undoped sample. The homogeneity of all the samples was discussed in detail by diffuse reflectance spectrum. This is the first time the reflection process is analysed for the cerium-doped ABT system to the best of our knowledge.

  18. Preparation of cerium-doped TiO2 film on 304 stainless steel and its bactericidal effect in the presence of sulfate-reducing bacteria (SRB)

    International Nuclear Information System (INIS)

    Cerium-doped TiO2 film with bactericidal activity was prepared on 304 stainless steel by a sol-gel process. The doped cerium ions were identified to have retarding effect on the phase transition from amorphous TiO2 to anatase TiO2. This effect was interpreted as the distortion of crystal lattice, due to the introduction of cerium ions into the crystal structure of TiO2. The absorption band edge of cerium-doped TiO2 film has a red shift compared with that of pure TiO2 film in UV-vis spectra. The films covered with sulfate-reducing bacteria (SRB) medium were exposed to sunlight for 6 h and the bactericidal efficiency was evaluated with most probable number technique. It was found that the bactericidal efficiency of cerium-doped TiO2 film and pure TiO2 film were 95% and 85%, respectively.

  19. Ab initio molecular dynamics study of the properties of cerium in liquid sodium at 1000 K temperature

    International Nuclear Information System (INIS)

    For liquid-sodium-cooled fast nuclear reactor systems, it is crucial to understand the behavior of lanthanides and other potential fission products in liquid sodium or other liquid metal solutions such as liquid cesium-sodium. In this study, we focus on lanthanide behavior in liquid sodium. Using ab initio molecular dynamics, we found that the solubility of cerium in liquid sodium at 1000 K was less than 0.78 at. %, and the diffusion coefficient of cerium in liquid sodium was calculated to be 5.57 × 10−9 m2/s. Furthermore, it was found that cerium in small amounts may significantly alter the heat capacity of the liquid sodium system. Our results are consistent with the experimental results for similar materials under similar conditions

  20. Ab initio molecular dynamics study of the properties of cerium in liquid sodium at 1000 K temperature

    Energy Technology Data Exchange (ETDEWEB)

    Samin, Adib; Li, Xiang; Zhang, Jinsuo [Nuclear Engineering Program, Department of Mechanical and Aerospace Engineering, The Ohio State University, 201 W 19th Avenue, Columbus, Ohio 43210 (United States); Mariani, R. D. [Idaho National Laboratory, Materials and Fuels Complex, Idaho Falls, Idaho 83415 (United States); Unal, Cetin [Los Alamos National Laboratory, P.O. Box 1663, Los Alamos, New Mexico 87545 (United States)

    2015-12-21

    For liquid-sodium-cooled fast nuclear reactor systems, it is crucial to understand the behavior of lanthanides and other potential fission products in liquid sodium or other liquid metal solutions such as liquid cesium-sodium. In this study, we focus on lanthanide behavior in liquid sodium. Using ab initio molecular dynamics, we found that the solubility of cerium in liquid sodium at 1000 K was less than 0.78 at. %, and the diffusion coefficient of cerium in liquid sodium was calculated to be 5.57 × 10{sup −9} m{sup 2}/s. Furthermore, it was found that cerium in small amounts may significantly alter the heat capacity of the liquid sodium system. Our results are consistent with the experimental results for similar materials under similar conditions.

  1. Ab initio molecular dynamics study of the properties of cerium in liquid sodium at 1000 K temperature

    Science.gov (United States)

    Samin, Adib; Li, Xiang; Zhang, Jinsuo; Mariani, R. D.; Unal, Cetin

    2015-12-01

    For liquid-sodium-cooled fast nuclear reactor systems, it is crucial to understand the behavior of lanthanides and other potential fission products in liquid sodium or other liquid metal solutions such as liquid cesium-sodium. In this study, we focus on lanthanide behavior in liquid sodium. Using ab initio molecular dynamics, we found that the solubility of cerium in liquid sodium at 1000 K was less than 0.78 at. %, and the diffusion coefficient of cerium in liquid sodium was calculated to be 5.57 × 10-9 m2/s. Furthermore, it was found that cerium in small amounts may significantly alter the heat capacity of the liquid sodium system. Our results are consistent with the experimental results for similar materials under similar conditions.

  2. An application of secondary ion mass spectrometry (SIMS) in studies of internal contamination micro localization of cerium

    International Nuclear Information System (INIS)

    Secondary Ion Mass Spectrometry (SIMS) permits the detection of stable and radioactive elements in micro volume. Based on the ablation of specimens by ion bombardment, this mass spectrometry method allows a rapid assessment of trace elements in biological samples. Its resolving mass power provides an efficient analytical method and, in particular, it makes possible accurate isotopic ratio determination. In this work, a particular example is presented on the basis of results obtained as a result of analyses of duodenal tissue sections from rats contaminated with cerium. Tests were performed with SIMS to localize cerium in tissue sections obtained from rats 12, 24 and 48 hours after contamination with this element. In all specimens groups, cerium was found in apical region of micro villus, with the exception of those obtained 48 h after contamination. In this report, strengths and limitations of SIMS are pointed out as well as the potential of SIMS in biological research. (author)

  3. A study of quantitative chemical state analysis on cerium surface by using auger electron spectroscopy and factor analysis

    International Nuclear Information System (INIS)

    A reaction with oxygen during oxygen exposure to Cerium metal surface under ultra high vacuum condition and depth profiling on formed Cerium oxide layer were investigated in term of chemical state analysis by Auger electron spectroscopy (AES) and by factor analysis. Principal component analysis (PCA) on Ce NON Auger spectra suggested that three physically meaningful components existed from the analyzed data in both cases. After the PCA, three spectra were extracted from the data and these showed significant peak shape changes in each spectrum which were corresponding to different chemical states. In addition, the profiles constructed by factor analysis showed the chemical state changes on the Cerium metal surface during oxidation or chemical depth distributions in the oxide layer. (author)

  4. Corrosion resistance of flaky aluminum pigment coated with cerium oxides/hydroxides in chloride and acidic electrolytes

    Science.gov (United States)

    Niroumandrad, S.; Rostami, M.; Ramezanzadeh, B.

    2015-12-01

    The objective of this study was to enhance the corrosion resistance of lamellar aluminum pigment through surface treatment by cerium oxides/hydroxides. The surface composition of the pigments was studied by energy-dispersive spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). The corrosion resistance of the pigment was evaluated by conventional hydrogen evolution measurements in acidic solution and electrochemical impedance spectroscopy (EIS) in 3.5% NaCl solution. Results showed that the Ce-rich coating composed of Ce2O3 and CeO2 was precipitated on the pigment surface after immersion in the cerium solution. The corrosion resistance of pigment was significantly enhanced after modification with cerium layer.

  5. Production of CeO2 Nanoparticles by Method of Laser Ablation of Bulk Metallic Cerium Targets in Liquid

    Science.gov (United States)

    Svetlichnyi, V. A.; Lapin, I. N.

    2016-03-01

    The method of pulsed laser ablation in liquid was used to synthesize dispersions of cerium oxide nanoparticles when subjecting a metallic cerium target in water and alcohol to basic frequency radiation of the nanosecond Nd:YAG laser (1064 nm, 7 ns, 20 Hz). Researchers have studied the effect of laser radiation parameters, duration of impact, and optical scheme of experiment on the ablation process. The average rate of nanoparticle production was 50 mg/h in water and 25 mg/h in alcohol. Researchers have studied the size characteristics and crystalline structure of the nanoparticles produced. The particles have bimodal size distribution with 6 nm and 25 nm maximums. The average crystallite size is 17-19 nm. The crystalline structure of nanoparticles, namely cubic cerium oxide (fluorite structure), space group Fm-3m, is confirmed by the X-ray diffraction data, as well as optical absorption spectra and Raman spectroscopy.

  6. Implementation of a complex multi-phase equation of state for cerium and its correlation with experiment

    Energy Technology Data Exchange (ETDEWEB)

    Cherne, Frank J [Los Alamos National Laboratory; Jensen, Brian J [Los Alamos National Laboratory; Elkin, Vyacheslav M [VNIITF

    2009-01-01

    The complexity of cerium combined with its interesting material properties makes it a desirable material to examine dynamically. Characteristics such as the softening of the material before the phase change, low pressure solid-solid phase change, predicted low pressure melt boundary, and the solid-solid critical point add complexity to the construction of its equation of state. Currently, we are incorporating a feedback loop between a theoretical understanding of the material and an experimental understanding. Using a model equation of state for cerium we compare calculated wave profiles with experimental wave profiles for a number of front surface impact (cerium impacting a plated window) experiments. Using the calculated release isentrope we predict the temperature of the observed rarefaction shock. These experiments showed that the release state occurs at different magnitudes, thus allowing us to infer where dynamic {gamma} - {alpha} phase boundary is.

  7. Catalytic activity of cerium-doped Ru/Al2O3 during ozonation of dimethyl phthalate

    Institute of Scientific and Technical Information of China (English)

    Yunrui ZHOU; Wanpeng ZHU; Xun CHEN

    2008-01-01

    In this paper, factors influencing the mineraliza-tion of dimethyl phthalate (DMP) during catalytic ozona-tion with a cerium-doped Ru/Al2O3 catalyst were studied. The catalytic contribution was calculated through the results of a companrison experiment. It showed that doping cerium significantly enhanced catalytic activity. The total organic carbon (TOC) removal over the doped catalyst at 100 rain reached 75.1%, 61.3% using Ru/Al2O3 catalyst and only 14.0% using ozone alone. Catalytic activity reached the maximum when 0.2% of ruthenium and 1.0% of cerium'were simultaneously loaded onto Al2O3 support. Results of experiments on oxidation by ozone alone, adsorption of the catalyst, Ce ion's and heterogeneous catalytic ozonation confirmed that the contribution of het-erogeneous catalytic ozonation was about 50%, which showed the obvious effect of Ru-Ce/Al2O3 on catalytic activity.

  8. Force modulation atomic force microscopy: background, development and application to electrodeposited cerium oxide films

    Science.gov (United States)

    Li, Feng-Bin; Thompson, G. E.; Newman, R. C.

    1998-04-01

    In force modulation atomic force microscopy (FMAFM), vertical oscillation of the scanning tip of the AFM is added purposely and the deflection of the tip, which is influenced by surface features of the sample, is used as the z dimension to construct images. FMAFM represents a powerful technique for scientific research, but its merit has not been realized adequately to date. In this paper, the basic principles and particular features, as well as potential drawbacks of the technique, are presented and demonstrated systematically, through its application to electrochemically deposited cerium oxide films. Comparisons are also made with the more familiar contact mode AFM (CMAFM) and tapping mode AFM (TMAFM). It is shown that FMAFM reveals the major topographic features of CMAFM, but affords (i) greater resolution for sample features that are difficult in CMAFM, and (ii) continuous two-dimensional mapping of local mechanical properties on a scale of nanometres that the CMAFM, TMAFM and any other techniques, are not capable of sensing. This information can be used to elucidate other properties of the investigated surface, such as crystallinity variation, phase separation and distribution, and mechanisms of formation of deposited films. Major artifacts associated with the technique include `wedge cavity effect' and `tip slip effect', for which a geometric model is proposed to elucidate their origins. The cerium oxide films are shown to be composed of relatively hard crystalline grains, of well-defined individual geometry and comparatively regular packing, alongside relatively soft amorphous patches, devoid of distinct geometry and assembled disorderly. These features are consistent with a nucleation and growth mechanism of the deposition, in which crystalline nuclei arise and grow from an intermediate cerium gel mass, produced in the interfacial region during deposition.

  9. Microstructure and mechanical properties of the Al-Ti alloy with cerium addition

    Directory of Open Access Journals (Sweden)

    L.A. Dobrzański

    2009-12-01

    Full Text Available Purpose: In this work there are presented the investigation results of mechanical properties and microstructure concerning mainly intermetallic phases of the aluminium – titanium alloy with a defined content of 2 and 4 % of cerium addition. The purpose of this work was also to determine the heat treatment conditions for solution heat treatment of the investigation alloys.Design/methodology/approach: The reason of this work was to determine the heat treatment influence, particularly solution heat treatment time to the changes of the microstructure, as well to determine which intermetallic phases occur after the heat treatment performed, and how is the morphology of these particles.Findings: After solution heat treatment for 4 hours the structure changes. The grains are larger and no more uniform as showed before. The most stable intermetallic in the Al-Ti system is the Al3Ti phase. The solution heat treatment time should be greater than 4 hours to ensure a proper solution of titanium and cerium in the Al-α solid solution.Research limitations/implications: The investigated aluminium samples were examined metallographically using optical microscope with different image techniques, scanning electron microscope and also analyzed using a Vickers micro-hardness tester, also EDS microanalysis was made.Practical implications: As an implication for the practice a new alloy can be developed, some other investigation should be performed in the future, but the knowledge found in this research shows an interesting investigation direction.Originality/value: The combination of light weight and high strength Ti-based alloys is very attractive for aerospace and automotive industries. Furthermore, the presence of calcium cerium into existence new unknown phases as well can enhance the thermal stability of ternary Al-Ti-Ce alloy because of its higher melting point then Al-Ti.

  10. High temperature stability of a 316 austenitic stainless steel coated with cerium oxide nanoparticles

    Science.gov (United States)

    Mendoza Del Angel, Humberto

    Cerium oxide (CeO2-x) nanoparticles were used for coating protection on a 316 Austenitic Stainless Steel (Aust. SS) to enhance the thermal stability of the oxide films formed at high temperatures. Three simple coating methods were used, dipping, spraying and spinning in order to explore the coating film morphology, nanoparticle distribution and its effect on thermal stability of the steel substrates. Experimentally, the selected steel was exposed to 800°C/1000°C under dry air conditions. Weight changes (DeltaW/A) were monitored as a function of time and the results were compared with uncoated alloys tested under similar conditions. The cerium oxide nanoparticles used on the three methods were synthesized in the laboratory obtaining nanoparticles in the range of 3.5 to 6.2 nanometers. It was found that cerium oxide particle size is affected by temperature. In this case, the activation energy for particle growth was estimated to be around 21,1 kJ/mol. Characterization of the film morphologies before and after oxidation were carried out using Atomic Force Microscopy (AFM), Surface Profilometry, Scanning Electron Microscopy (SEM) and X-ray Diffraction (XRD). A comparison of the three coating methods was carried out for the particular case of the 316 Aust. SS coupons. In addition, the oxidation kinetics was experimentally investigated for the coated samples. For this purpose thermal gravimetric determinations were made at 800°C, 900°C, and 1000°C and oxidation rate constants were calculated at each temperature.

  11. Catalytic wet peroxidation of pyridine bearing wastewater by cerium supported SBA-15

    Energy Technology Data Exchange (ETDEWEB)

    Subbaramaiah, V. [Department of Chemical Engineering, Indian Institute of Technology Roorkee, Roorkee 247667 Uttarakhand (India); Srivastava, Vimal Chandra, E-mail: vimalcsr@yahoo.co.in [Department of Chemical Engineering, Indian Institute of Technology Roorkee, Roorkee 247667 Uttarakhand (India); Mall, Indra Deo [Department of Chemical Engineering, Indian Institute of Technology Roorkee, Roorkee 247667 Uttarakhand (India)

    2013-03-15

    Highlights: ► Cerium supported SBA-15 (Ce/SBA-15) synthesized by two-step synthesis. ► Characterization of Ce/SBA-15 by FTIR, XRD and BET surface area. ► Catalytic peroxidation of pyridine by Ce/SBA-15. ► Optimization of parameters like catalyst dose, H{sub 2}O{sub 2} dose, initial concentration and temperature. ► Catalyst reusability and leaching study performed. -- Abstract: Cerium supported SBA-15 (Ce/SBA-15) was synthesized by two-step synthesis method in acidic medium. It was further characterized by various characterization techniques such as X-ray diffraction, field-emission scanning electron microscopy, Fourier transform infrared spectroscopy and N{sub 2} adsorption–desorption pore size distribution analysis. The Ce/SBA-15 showed highly ordered meso-structure with pore diameter ≈ 70–100 A and pore volume ≈ 0.025 cm{sup 3}/g. Ce/SBA-15 was further evaluated as a catalyst for the oxidation of highly toxic and non-biodegradable material, pyridine, by catalytic wet-peroxidation method. The effects of various operating parameters such as catalyst dose (0.5–6 g/l), stoichiometric ratio of H{sub 2}O{sub 2}/pyridine (1–6), initial pyridine concentration (50–800 mg/l) and temperature (313–358 K) have been evaluated and optimized. Ce/SBA-15 showed stable performance during reuse for six cycles with negligible cerium leaching. Kinetic and thermodynamic parameters and operation cost have also been determined.

  12. Biosorption of lanthanum and cerium from aqueous solutions using tangerine (Citrus reticulata) peel: Equilibrium, kinetic, and thermodynamic studies

    OpenAIRE

    Torab-Mostaedi Meisam

    2013-01-01

    Biosorption of lanthanum (III) and cerium (III) from aqueous solution by tangerine (Citrus reticulate) peel has been investigated in a batch system as a function of pH, biosorbent dosage, contact time, and temperature. The equilibrium pH was found to severely affect the biosorption performance; pH 5.0 is found to be an optimum pH for favorable biosorption of La (III) and Ce (III). The biosorption of lanthanum and cerium was investigated by the Langmuir, Freundlich and Dubinin-Radushkevi...

  13. Changes in Physiological and Agronomical Parameters of Barley (Hordeum vulgare) Exposed to Cerium and Titanium Dioxide Nanoparticles

    OpenAIRE

    Luca Marchiol; Alessandro Mattiello; Filip Pošćić; Guido Fellet; Costanza Zavalloni; Elvio Carlino; Rita Musetti

    2016-01-01

    The aims of our experiment were to evaluate the uptake and translocation of cerium and titanium oxide nanoparticles and to verify their effects on the growth cycle of barley (Hordeum vulgare L.). Barley plants were grown to physiological maturity in soil enriched with either 0, 500 or 1000 mg·kg−1 cerium oxide nanoparticles (nCeO2) or titanium oxide nanoparticles (nTiO2) and their combination. The growth cycle of nCeO2 and nTiO2 treated plants was about 10 days longer than the controls. In nC...

  14. Improvement of corrosion resistance of AZ31 Mg alloy by anodizing with co-precipitation of cerium oxide

    Institute of Scientific and Technical Information of China (English)

    Salah Abdelghany SALMAN; Ryoichi ICHINO; Masazumi OKIDO

    2009-01-01

    Anodizing of AZ31 Mg alloy in NaOH solution by co-precipitation of cerium oxide was investigated. The chemical composition and phase structure of the coating film were determined via optical microscopy, SEM and XRD. The corrosion properties of the anodic film were characterized by using potentiodynamic polarization curves in 17 mmol/L NaCl and 0.1 mol/L Na2SO4 solution at 298 K. The corrosion resistance of AZ31 magnesium alloy is significantly improved by adding cerium oxide to alkaline solution. In addition, the surface properties are enhanced and the film contains no crack.

  15. In situ growth of blue-emitting thin films of cerium-doped barium chloride hydrate at low temperatures

    OpenAIRE

    J. Hao; LOU, Z; Cocivera, M

    2003-01-01

    Blue emission was observed from thin films of barium chloride hydrate doped with cerium. The films were deposited by spray pyrolysis of aqueous solutions with substrate temperatures between 250 and 450°C. The cathodoluminescence (CL) spectrum consists of two peaks at 443 and 485 nm due to 4f-5d transitions of cerium ion. The dependence of the emission band on deposition temperature and Ce/Ba ratio is discussed. The CL luminance and luminous efficiency at 5 kV were 120 cd/m² and 0.48 lm/W, res...

  16. Iranian natural clinoptilolite and its synthetic zeolite P for removal of cerium and thorium from nuclear wastewaters

    International Nuclear Information System (INIS)

    The ion-exchange behaviors of an Iranian natural clinoptilolite and its modified forms as well as a relevant synthetic zeolite P were investigated toward cerium and thorium from nuclear wastewaters. Column experiments were performed on different exchangers in various conditions and the effect of parameters such as particle size, pH, temperature, and time were considered. The distribution coefficient, cation exchange capacity and some thermodynamic parameters were calculated. Ion-exchange isotherms and break-through curves were plotted. As a result, the selectivity of synthetic zeolite P from Iranian natural clinoptilolite toward cerium and thorium was compared with that of natural and cationic forms of clinoptilolite. (author)

  17. APPLICATIONS OF CERIUM BIS (MONOMYRISTY—LPHOSPHATE)ADSORBENT TO REVERSED PHASE LIQUID CHROMATOGRAPHY

    Institute of Scientific and Technical Information of China (English)

    SuZhengquan; FengHuixia; 等

    1996-01-01

    The tetravalent metal salts of monoalkyl phosphates [M(O3POR)2]are a new kind of stationary phases of Chromatography-homogeneous bonded phases.This paper deals with the application of cerium bis(monomyristylphosphate)as support to reversed phase liquid chromatography.The results show that the best mobil phase is CH3CN:H2O=95:5.The good separation to the mixture containing six aromatic hydrocarbons and the determination of naphthalene in a group samples have been achieved.The regression analysis shows that detect limits,linearities and precision for six aromatic hydrocarbons are good.

  18. Characteristics of cerium-gadolinium oxide (CGO) suspensions as a function of dispersant and powder properties

    DEFF Research Database (Denmark)

    Phair, John; Lönnroth, Nadja; Lundberg, Mats;

    2009-01-01

    A series of concentrated suspensions ( = 0.18–0.34) of cerium-gadolinium oxide (CGO) in terpineol were prepared as a function of dispersant, powder surface area and solids concentration. The stability of the suspensions was assessed by rheological measurements including viscosity and oscillatory...... measurements. Six dispersants with different molecular weights and terminal groups were compared for their relative efficiency in dispersing the powders by viscosity measurements. A Rhodafac dispersant, a long chain polymer containing phosphoric acid terminal groups, was found to produce suspensions with the...

  19. Kinetics of bromide catalysed oxidation of dextrose by cerium (IV) in aqueous sulphuric acid solution

    International Nuclear Information System (INIS)

    Kinetics of bromide catalysed oxidation of dextrose by CeIV in aqueous sulphuric acid medium show first order dependence each in dextrose and cerium(IV). The reaction rate decreases on increasing the concentration of hydrogen ion. The increase in [HSO4-] or [SO42-] decreases the rate. The bromide ion shows positive catalytic effect on the reaction rate. The value of activation energy has been calculated and a suitable mechanism confirming to the kinetic data is proposed. (author). 3 refs., 3 tabs

  20. Trace electrochemical analysis of Europium, Ytterbium, and Cerium at their joint presence in solution

    Directory of Open Access Journals (Sweden)

    Rema Matakova

    2012-03-01

    Full Text Available In the course of several decades at the department of analytical chemistry and chemistry of rare elements there were studied the electrode processes with participation of rare-earth metals (REM in accordance with the long awaiting problem of the development of rare-metal and rare-earth branch of non-ferrous metallurgy of Kazakhstan. With the aim of express and highly sensitive analytical control of raw materials and final product of rare-earth industry there were developed the methods of inversion-voltamperometric determination of low concentrations of europium, ytterbium and cerium under the conditions of their individual and combined presence in the solution.

  1. Sequence-specific Hydrolysis of Single-stranded DNA by PNA-Cerium (Ⅳ) Adduct

    Institute of Scientific and Technical Information of China (English)

    He Bai SHEN; Feng WANG; Yong Tao YANG

    2005-01-01

    A novel artificial site specific cleavage reagent, with peptide nucleic acid (PNA) as sequence-recognizing moiety and cerium (Ⅳ) ions as "scissors" for cleaving target DNA, was synthesized. Subsequently, it was employed in the cleavage of target 26-mer single-stranded DNA (ssDNA), which has 10-mer sequence complementary with PNA recognizer in the hybrids,under physiological conditions. Reversed-phase high-performance liquid chromatogram (RPHPLC) experiments indicated that the artificial site specific cleavage reagent could cleave the target DNA specifically.

  2. Preparation and electrochemical study of cerium-silica sol-gel thin films

    International Nuclear Information System (INIS)

    Design and development of suitable multilayered systems for delaying corrosion advance in metals requires that both the alteration mechanisms of the metal and the behaviour and properties of the protective coatings be known. Coatings prepared by the sol-gel method provide a good approach as protective layers on metallic surfaces. This kind of coatings can be prepared from pure chemical reagents at room temperature and atmospheric pressure, with compositions in a very wide range of environmentally non-aggressive precursors. Sol-gel coatings based on siloxane bonded units were prepared starting from an organic-inorganic hybrid system. The precursors were γ-methacryloxypropyltrimethoxysilane (MAP) and tetramethoxysilane (TMOS). Cerium nitrate hexahydrate in three different concentrations was added. Cerium salts may perform a similar protective effect to that carried out by the well-known lead oxides and chromium salts, even though in this case a negative environmental impact is not expected. Application of coatings upon pure zinc substrates and common glass slides were performed by spinning. Coated samples were heat treated at 40 deg. C for 6 days. Optical measurements (UV-Vis absorption and diffuse reflectance spectroscopies) pointed out that the coatings were colourless and transparent, reducing the diffuse reflectance of the metallic surface up to ∼60%. Optical and scanning electron microscopies (SEM) allowed observation of the texture and microstructure of the coated samples, both before and after the corrosion tests were carried out. Likewise, the remaining sols were kept to gelify at 60 deg. C for 4 days and then powdered to obtain suitable samples for analysing them by other characterisation techniques (Fourier transformed infrared, FTIR and differential thermal analysis, DTA). Electrochemical measurements were performed by impedance spectroscopy. This technique was used to clarify the anticorrosive protection role of cerium ions incorporated into the hybrid

  3. Cerium and europium doped ZnO thin films fabricated by pulsed laser deposition

    Czech Academy of Sciences Publication Activity Database

    Novotný, Michal; Fitl, P.; Bulíř, Jiří; Marešová, E.; Hruška, P.; Guille, A.; Guy, S.; Drahokoupil, Jan; Fekete, Ladislav; Lančok, Ján

    Lille: European Materials Research Society, 2014 - (Lippert, T.). J-24-J-24 [E- MRS 2014 Spring Meeting. 26.05.2014-30.05.2014, Lille] R&D Projects: GA MŠk(CZ) LM2011029; GA ČR(CZ) GAP108/11/0958; GA MŠk(CZ) 7AMB14FR010 Grant ostatní: AVČR(CZ) M100101271 Institutional support: RVO:68378271 Keywords : cerium * europium * ZnO * thin film * pulsed laser deposition Subject RIV: BM - Solid Matter Physics ; Magnetism

  4. Performance of a Tungsten-Cerium Fluoride Sampling Calorimeter in High-Energy Electron Beam Tests

    CERN Document Server

    Becker, R; Dissertori, G; Djambazov, L; Donegà, M; Lustermann, W; Marini, A C; Nessi-Tedaldi, F; Pandolfi, F; Peruzzi, M; Schönenberger, M; Cavallari, F; Dafinei, I; Diemoz, M; Lope, C Jorda; Meridiani, P; Nuccetelli, M; Paramatti, R; Pellegrino, F; Micheli, F; Organtini, G; Rahatlou, S; Soffi, L; Brianza, L; Govoni, P; Martelli, A; de Fatis, T Tabarelli; Monti, V; Pastrone, N; Trapani, P P; Candelise, V; Della Ricca, G

    2015-01-01

    A prototype for a sampling calorimeter made out of cerium fluoride crystals interleaved with tungsten plates, and read out by wavelength-shifting fibres, has been exposed to beams of electrons with energies between 20 and 150 GeV, produced by the CERN Super Proton Synchrotron accelerator complex. The performance of the prototype is presented and compared to that of a Geant4 simulation of the apparatus. Particular emphasis is given to the response uniformity across the channel front face, and to the prototype's energy resolution.

  5. Preparation of mesoporous cerium oxide templated by tri-block copolymer for solid oxide fuel cell

    International Nuclear Information System (INIS)

    Mesoporous structured CeO2 with high specific surface area was synthesized at ambient temperature in this study. The synthesis of this material was accomplished using a tri-block copolymer as the organic supermolecular template and the cerium nitrate hexahydrate as the inorganic precursor. X-ray diffraction, nitrogen adsorption and desorption isotherms and transmission electron microscopy have been used to characterize the mesoporous structure. The nitrogen adsorption and desorption isotherms analysis indicates that the average pore size is 3.5 and 3.4 nm and the specific surface area is 155 and 103 m2/g for the samples calcined at 523 and 723 K, respectively

  6. UV-Shielding and Catalytic Characteristics of Nanoscale Zinc-Cerium Oxides

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Fine particles of zinc-cerium oxides (ZCO) used as an ultraviolet filter were prepared via combustion synthesis route. The catalytic activity, UV-shielding performance, surface modification and application of ZCO in polyester varnish were discussed in detail. The experimental results indicate that the photo-catalytic activity of ZCO is much smaller than these of ZnO and TiO2; the oxidation catalytic activity of ZCO is far lower than that of CeO2; the ZCO has shown excellent ultraviolet absorption in the range of UV;addition modified ZCO (MZCO) into polyester will enhance the UV-shielding capability of polyester.

  7. High-resolution photoemission study of γ- and α-cerium

    International Nuclear Information System (INIS)

    High-resolution photoemission studies on the α and γ phases of cerium show changes in the binding energies of the two 4f-related features. The location of the two 4f-related features in the γ phase are at -0.2 and -2.0 eV, while in the α phase these features are located at the Fermi level and -2.1 eV. These results are a direct test of the theories proposed to explain the presence of the two features

  8. The low-aluminium cast iron of reduced silicon content treated with cerium mischmetal

    OpenAIRE

    M. S. Soiński; P. Susek; Hübner, K.; P. Mierzwa

    2008-01-01

    The work presents the effect of cerium mischmetal used in quantities of 0.1 and 0.2 wt-% and ferrosilicon used in quantities from 0.5% to 1.5% on the alloy matrix and the shape of graphite precipitates in the low-aluminium cast iron from seven heats, basing on the examination of its structure. The hypereutectic cast iron of the relatively high carbon content (4.0÷4.2%) at the prior-to-treatment silicon and manganese content equal to ca. 0.6% and ca. 0.04%, respectively, has been examined.It h...

  9. Multipurpose Compound

    Science.gov (United States)

    1983-01-01

    Specially formulated derivatives of an unusual basic compound known as Alcide may be the answer to effective treatment and prevention of the disease bovine mastitis, a bacterial inflammation of a cow's mammary gland that results in loss of milk production and in extreme cases, death. Manufactured by Alcide Corporation the Alcide compound has killed all tested bacteria, virus and fungi, shortly after contact, with minimal toxic effects on humans or animals. Alcide Corporation credits the existence of the mastitis treatment/prevention products to assistance provided the company by NERAC, Inc.

  10. Impact of cerium oxide nanoparticles on cilantro ( Coriandrum sativum)

    Science.gov (United States)

    Morales, Maria Isabel

    Studies have shown that plants exposed to ENPs suffer different types of stress. Other studies have revealed that plants can take up and accumulate CeO2 NPs without modification. Thus, these NPs could enter the food chain through edible plants, posing a threat for human health. Cilantro (Coriandrum sativum) is a worldwide culinary and medicinal plant consumed either as a fresh herb or a spice. In this research, cilantro plants were germinated and cultivated for 30 days in organic soil treated with CeO2 NPs at concentrations varying from 0 to 500 mg kg -1. Subsequently, plant organs were analyzed by using spectroscopic techniques and biochemical assays. Results indicate that at 125 mg kg -1, the CeO2 NPs significantly increased the root size compared with the other treatments. The ICP-OES results showed that plants exposed to 500 mg kg-1 had significantly (p ≤ 0.05) more Ce in shoots and roots compared to the other treatments. Results from the biochemical assays showed that at 125 mg kg-1, catalese activity significantly increased in shoots and ascorbate peroxidase in roots (p ≤ 0.05). In addition, the FTIR analyses revealed that at 125 mg kg-1, the CeO2 NPs changed the chemical environment of the carbohydrates within the cilantro shoots, for which changes in the area of the stretching frequencies were observed. Moreover, analyses of antioxidant compounds showed a significant ( p ≤ 0.05) reduction on total phenolic content in shoots of cilantro plants treated with 500 mg CeO2 NPs kg-1 . This suggests that the CeO2 NPs have the potential to diminish the ability of cilantro plants to scavenge reactive oxygen species. The multi-elemental analysis showed that plants treated with CeO2 at the 500 mg kg-1 treatment had a significant ( p ≤ 0.05) reduction in shoots' sulfur, silicon, and zinc accumulation. The results of this research indicate that the CeO2 NPs at 500 mg CeO2 kg-1 concentration cause a reduction in the antioxidant ability and nutritional properties

  11. Effects of cerium oxide supplementation to laying hen diets on performance, egg quality, some antioxidant enzymes in serum and lipid oxidation in egg yolk.

    Science.gov (United States)

    Bölükbaşı, S C; Al-Sagan, A A; Ürüşan, H; Erhan, M K; Durmuş, O; Kurt, N

    2016-08-01

    This study was conducted to determine the effects of dietary cerium oxide levels (0, 100, 200, 300 or 400 mg/kg) on the laying performance, egg quality, some blood serum parameters and egg lipid peroxidation of laying hen. In total, one hundred and twenty 22-week-old brown Lohman LSL laying hens were randomly assigned to five groups equally (n = 24). Each treatment was replicated six times. Dietary supplementation of cerium oxide had no significant effect on feed intake and egg weight. The addition of cerium oxide to the laying hens' feed improved feed conversion ratio and increased (p laying hens feed led to a significant (p hen diets. It was also observed that serum superoxide dismutase (SOD) activity and malondialdehyde (MDA) concentration decreased significantly with supplementation of cerium oxide in diets. Inclusion of cerium oxide resulted in a significant reduction in thiobarbituric acid reactive substance (TBARS) values in egg yolk in this study. It can be concluded that the addition of cerium oxide had positive effects on egg production, feed conversion ratio and egg shelf life. Based on the results of this study, it could be advised to supplement laying hens feed with cerium oxide as feed additives. PMID:26847677

  12. Effect of cerium on structure modifications of a hybrid sol–gel coating, its mechanical properties and anti-corrosion behavior

    International Nuclear Information System (INIS)

    Highlights: ► New sol–gel routes to replace chromates for corrosion protection of aluminum. ► Effect of cerium concentration on the microstructure of xerogel. ► Electrochemical and mechanical performances of hybrid coating with different cerium contents. ► Good correlation between the different results with an optimal cerium content of 0.01 M. -- Abstract: An organic–inorganic hybrid coating was developed to improve the corrosion resistance of the aluminum alloy AA 2024-T3. Organic and inorganic coatings derived from glycidoxypropyl-trimethoxysilane (GPTMS) and aluminum tri-sec-butoxide Al(OsBu)3, with different cerium contents, were deposited onto aluminum by dip-coating process. Corrosion resistance and mechanical properties were investigated by electrochemical impedance measurements and nano-indentation respectively. An optimal cerium concentration of 0.01 M was evidenced. To correlate and explain the hybrid coating performances in relation to the cerium content, NMR experiments were performed. It has been shown that when the cerium concentration in the hybrid is higher than 0.01 M there are important modifications in the hybrid structure that account for the mechanical properties and anti-corrosion behavior of the sol–gel coating.

  13. Characterization of microstructure and catalytic of cerium oxide obtained by colloidal solution; Caracterizacao da microestrutura e da atividade catalitica de oxido de cerio obtido por solucao coloidal

    Energy Technology Data Exchange (ETDEWEB)

    Senisse, C.A.L.; Bergmann, C.P.; Alves, A.K., E-mail: carolinasenisse@hotmail.com [Universidade Federal do Rio Grande do Sul (UFRGS), Porto Alege, RS (Brazil). Lab. de Materiais Ceramicos

    2012-07-01

    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)

  14. Effect of cerium on structure modifications of a hybrid sol–gel coating, its mechanical properties and anti-corrosion behavior

    Energy Technology Data Exchange (ETDEWEB)

    Cambon, Jean-Baptiste, E-mail: cambon@chimie.ups-tlse.fr [Institut Carnot CIRIMAT, Université de Toulouse, UMR CNRS 5085, 118 Route de Narbonne, 31062 Toulouse Cedex 9 (France); Esteban, Julien; Ansart, Florence; Bonino, Jean-Pierre; Turq, Viviane [Institut Carnot CIRIMAT, Université de Toulouse, UMR CNRS 5085, 118 Route de Narbonne, 31062 Toulouse Cedex 9 (France); Santagneli, S.H.; Santilli, C.V.; Pulcinelli, S.H. [Departamento Fısico-Química, Instituto de Química, Universidade Estadual Paulista, UNESP, CP 355, 14801-970 Araraquara, SP (Brazil)

    2012-11-15

    Highlights: ► New sol–gel routes to replace chromates for corrosion protection of aluminum. ► Effect of cerium concentration on the microstructure of xerogel. ► Electrochemical and mechanical performances of hybrid coating with different cerium contents. ► Good correlation between the different results with an optimal cerium content of 0.01 M. -- Abstract: An organic–inorganic hybrid coating was developed to improve the corrosion resistance of the aluminum alloy AA 2024-T3. Organic and inorganic coatings derived from glycidoxypropyl-trimethoxysilane (GPTMS) and aluminum tri-sec-butoxide Al(O{sup s}Bu){sub 3}, with different cerium contents, were deposited onto aluminum by dip-coating process. Corrosion resistance and mechanical properties were investigated by electrochemical impedance measurements and nano-indentation respectively. An optimal cerium concentration of 0.01 M was evidenced. To correlate and explain the hybrid coating performances in relation to the cerium content, NMR experiments were performed. It has been shown that when the cerium concentration in the hybrid is higher than 0.01 M there are important modifications in the hybrid structure that account for the mechanical properties and anti-corrosion behavior of the sol–gel coating.

  15. Mixed mode and sequential oscillations in the cerium-bromate-4-aminophenol photoreaction

    Science.gov (United States)

    Bell, Jeffrey G.; Wang, Jichang

    2013-09-01

    Cerium was introduced to the bromate-aminophenol photochemical oscillator to implement coupled autocatalytic feedbacks. Mixed mode and sequential oscillations emerged in the studied system, making it one of the few chemical oscillators known to support consecutive bifurcations in a batch system. The complex reaction behavior showed a strong dependence on the intensity of illumination supplied to the system. Removal of illumination during an oscillatory window affected both the frequency and amplitude of the oscillation but did not fully extinguish them, indicating that the cerium-bromate-4-aminophenol oscillator was photosensitive rather than photo-controlled. A moderate light intensity allowed for a slow evolution of the system, which proved to be critical for the emergence of transient complex oscillations. Variation of individual reaction parameters was carried out, which indicated that the development of complex oscillations occur in a narrow region and a phase diagram in the 4-aminophenol and sulfuric acid plane demonstrated this. Simulations provide strong support that transient complex oscillations observed experimentally arise from the coupling of two autocatalytic cycles.

  16. Mixed mode and sequential oscillations in the cerium-bromate-4-aminophenol photoreaction

    Energy Technology Data Exchange (ETDEWEB)

    Bell, Jeffrey G.; Wang Jichang [Department of Chemistry and Biochemistry, University of Windsor, Windsor, Ontario N9B 3P4 (Canada)

    2013-09-15

    Cerium was introduced to the bromate-aminophenol photochemical oscillator to implement coupled autocatalytic feedbacks. Mixed mode and sequential oscillations emerged in the studied system, making it one of the few chemical oscillators known to support consecutive bifurcations in a batch system. The complex reaction behavior showed a strong dependence on the intensity of illumination supplied to the system. Removal of illumination during an oscillatory window affected both the frequency and amplitude of the oscillation but did not fully extinguish them, indicating that the cerium-bromate-4-aminophenol oscillator was photosensitive rather than photo-controlled. A moderate light intensity allowed for a slow evolution of the system, which proved to be critical for the emergence of transient complex oscillations. Variation of individual reaction parameters was carried out, which indicated that the development of complex oscillations occur in a narrow region and a phase diagram in the 4-aminophenol and sulfuric acid plane demonstrated this. Simulations provide strong support that transient complex oscillations observed experimentally arise from the coupling of two autocatalytic cycles.

  17. Mixed mode and sequential oscillations in the cerium-bromate-4-aminophenol photoreaction

    International Nuclear Information System (INIS)

    Cerium was introduced to the bromate-aminophenol photochemical oscillator to implement coupled autocatalytic feedbacks. Mixed mode and sequential oscillations emerged in the studied system, making it one of the few chemical oscillators known to support consecutive bifurcations in a batch system. The complex reaction behavior showed a strong dependence on the intensity of illumination supplied to the system. Removal of illumination during an oscillatory window affected both the frequency and amplitude of the oscillation but did not fully extinguish them, indicating that the cerium-bromate-4-aminophenol oscillator was photosensitive rather than photo-controlled. A moderate light intensity allowed for a slow evolution of the system, which proved to be critical for the emergence of transient complex oscillations. Variation of individual reaction parameters was carried out, which indicated that the development of complex oscillations occur in a narrow region and a phase diagram in the 4-aminophenol and sulfuric acid plane demonstrated this. Simulations provide strong support that transient complex oscillations observed experimentally arise from the coupling of two autocatalytic cycles

  18. Elasticity of cerium up to 4.4 GPa by sound velocity measurements under hydrostatic pressure

    International Nuclear Information System (INIS)

    We report here the longitudinal and shear sound velocities on polycrystalline cerium under hydrostatic pressure across the iso-structural γ-α phase transition up to 4.4 GPa. Comparing with previous methods, the pressure-density relation of Ce has been calculated by integrating with the initial travel time and pressure without any fitting. The pressure correction of the Grüneisen parameter and linear expansion coefficient are taken into account during the integration process. The sound velocities, bulk modulus, shear modulus, Debye temperature, and vibrational entropy are achieved and have been compared with previous results. The bulk modulus of cerium in α phase agrees with the previous results determined by neutron and x-ray diffraction. The Debye temperature above and below the phase transition are θDγ=130.9 K and θDα=151.9 K, respectively. The difference of the Debye temperature from respective experiment is found and has been expounded. We consider that the vibrational entropy change per atom of 0.44 k B as the Kondo collapse of 17% volume change, and 0.70 k B as the total change from γ phase to complete α phase. (papers)

  19. 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)

  20. Dielectric properties and electronic transitions of porous and nanostructured cerium oxide films

    International Nuclear Information System (INIS)

    Cerium dioxide (CeO2) exhibits exceptional electronic properties such as optical transparency and high refractive index (n) and high dc dielectric constant (k). Therefore, it is an attractive material for ultra-thin gate oxide in CMOS technology, where high-k dielectrics are required. We study the electronic properties of nanostructured and porous cerium oxide (CeOx) films, 110-500 nm thick, grown on Si by electron beam evaporation (EBE) and ion beam assisted deposition (IBAD). The film microstructure and morphology (grain size, porosity, defect concentration, surface and interface roughness) are controlled by varying the process parameters appropriately. They have been studied by high-resolution and transmission electron microscopy (HRTEM). The optical properties have been studied by spectroscopic ellipsometry (SE) and k was determined by capacitance measurements. We have found that the values of k and n (1.6-2.5 depending on porosity) are affected by the electronic transitions, which are strongly correlated with the microstructure and morphology of the films. We investigate how the microstructure and morphology variations affect the absolute values of the dc dielectric constant and of the dielectric function at the UV-Vis and IR spectral regions. In addition, we investigate the very important role of the defects, which have the form of grain boundaries, trivalent Ce3+ and O vacancies. As a result we were able to tailor n and k of CeOx films controlling their porosity and defect density

  1. FT-IR Studies of Cerium Oxide Nanoparticles and Natural Zeolite Materials

    Directory of Open Access Journals (Sweden)

    Oana Lelia Pop

    2015-05-01

    Full Text Available An emerging topic of our days is nanoscience and nanotechnology successfully applied in the food industry. Characteristics such as size, surface area and morphology can modify the basic properties and the chemical reactivity of the nanomaterials. The breakthrough of innovative materials, processes, and phenomena at the nanoscale, as well as the progress of new experimental and theoretical techniques for research, supply novel opportunities for the expansion of original nanosystems and nanostructured materials. These study examine two types of nanoparticles, namely cerium oxide nanoparticles (CeO2 NP and natural zeolites. In view of the importance of CeO2 NP in various biological applications, the primary objective of this study is to characterise four samples of CeO2 NP in order to understand the role of the synthesis process in the final product. Nanocrystalline natural zeolites are materials with interesting properties which allows them to be used as adjuvant in many therapies. The characterisation of CeO2 NP and two types of natural zeolites using Fourier Transform Infrared (FT-IR spectroscopy is described. Therefore, this study examined two types of nanomaterials, namely cerium oxide nanoparticles and zeolites, for further applications on microorganisms and living cells.

  2. Direct liquid injection chemical vapor deposition of platinum doped cerium oxide thin films

    Energy Technology Data Exchange (ETDEWEB)

    Zanfoni, N.; Avril, L.; Imhoff, L.; Domenichini, B., E-mail: bruno.domenichini@u-bourgogne.fr; Bourgeois, S.

    2015-08-31

    Thin films of Pt-doped CeO{sub 2} were grown by direct liquid injection chemical vapor deposition on silicon wafer covered by native oxide at 400 °C using Ce(IV) alkoxide and organoplatinum(IV) as precursors. X-ray photoelectron spectra evidenced that the platinum oxidation state is linked to the deposition way. For platinum deposited on top of cerium oxide thin films previously grown, metallic platinum particles were obtained. Cerium and platinum codeposition allowed obtaining a Pt{sup 0} and Pt{sup 2+} mixture with the Pt{sup 2+} to Pt ratio strongly dependent on the platinum flow rate during the deposition. Indeed, the lower the platinum precursor flow rate is, the higher the Pt{sup 2+} to Pt ratio is. Moreover, surface and cross-sectional morphologies obtained by scanning electron microscopy evidenced porous layers in any case. - Highlights: • Pt-doped ceria were synthesized. • Films were obtained by direct liquid injection chemical vapor deposition. • Simultaneous deposition of Pt and Ce was used to obtain homogeneous films. • Pt{sup 2+} was revealed through X-ray photoelectron spectroscopy. • Different routes were used to exalt Pt{sup 2+}/Pt ratio.

  3. Growth mode and oxidation state analysis of individual cerium oxide islands on Ru(0001)

    International Nuclear Information System (INIS)

    The growth of cerium oxide on Ru(0001) by reactive molecular beam epitaxy has been investigated using low-energy electron microscopy (LEEM) and diffraction as well as local valence band photoemission. The oxide islands are found to adopt a carpet-like growth mode, which depending on the local substrate morphology and misorientation leads to deviations from the otherwise almost perfect equilateral shape at a growth temperature of 850 °C. Furthermore, although even at this high growth temperature the micron-sized CeO2(111) islands are found to exhibit different lattice registries with respect to the hexagonal substrate, the combination of dark-field LEEM and local intensity-voltage analysis reveals that the oxidation state of the islands is homogeneous down to the 10 nm scale. - Highlights: • Cerium oxide is grown on ruthenium inside a low-energy electron microscope (LEEM). • The identified carpet growth mode is shown to determine the oxide island shape. • Intensity-voltage LEEM is demonstrated to be sensitive to oxidation state changes. • The oxidation state is found to be laterally homogeneous on the nanometer scale. • Ceria islands of the same oxidation state may have different substrate registries

  4. Direct liquid injection chemical vapor deposition of platinum doped cerium oxide thin films

    International Nuclear Information System (INIS)

    Thin films of Pt-doped CeO2 were grown by direct liquid injection chemical vapor deposition on silicon wafer covered by native oxide at 400 °C using Ce(IV) alkoxide and organoplatinum(IV) as precursors. X-ray photoelectron spectra evidenced that the platinum oxidation state is linked to the deposition way. For platinum deposited on top of cerium oxide thin films previously grown, metallic platinum particles were obtained. Cerium and platinum codeposition allowed obtaining a Pt0 and Pt2+ mixture with the Pt2+ to Pt ratio strongly dependent on the platinum flow rate during the deposition. Indeed, the lower the platinum precursor flow rate is, the higher the Pt2+ to Pt ratio is. Moreover, surface and cross-sectional morphologies obtained by scanning electron microscopy evidenced porous layers in any case. - Highlights: • Pt-doped ceria were synthesized. • Films were obtained by direct liquid injection chemical vapor deposition. • Simultaneous deposition of Pt and Ce was used to obtain homogeneous films. • Pt2+ was revealed through X-ray photoelectron spectroscopy. • Different routes were used to exalt Pt2+/Pt ratio

  5. Surface study of cerium oxide based coatings obtained by cathodic electrodeposition on zinc

    International Nuclear Information System (INIS)

    A surface study of electrodeposited cerium oxide based coatings is presented. Different surface analytical techniques were used in order to obtain complementary information to fully characterize such complex systems. X-ray Photoelectron Spectroscopy was used as the main technique to determine the surface composition of the coating. The analysis of the core level peaks of the elements provides additional information about the functional groups present on the surface. A mixture of Ce (III) and Ce (IV) was found in the coating and their proportion was calculated at different depths. The analysis of the O 1s core level peak revealed a triple structure whose origin will be discussed. To support the results obtained, electron stimulated desorption was performed. The study was completed with Auger electron spectroscopy and Raman spectroscopy, both techniques having different surface sensitivities. From all these results, it is derived that incomplete electrochemical reactions occurred during the growth of the coatings. This led to rather complex compositions, in which defective cerium oxides are the major species. In addition, hydroxides, carbonates and nitrates are also present, together with adsorbed water.

  6. Surface study of cerium oxide based coatings obtained by cathodic electrodeposition on zinc

    Energy Technology Data Exchange (ETDEWEB)

    Martinez, L., E-mail: lidia.martinez@icmm.csic.es [Instituto de Ciencia de Materiales de Madrid (ICMM-CSIC), Cantoblanco, 28049 Madrid (Spain); Roman, E.; Segovia, J.L. de [Instituto de Ciencia de Materiales de Madrid (ICMM-CSIC), Cantoblanco, 28049 Madrid (Spain); Poupard, S.; Creus, J.; 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)

    2011-05-01

    A surface study of electrodeposited cerium oxide based coatings is presented. Different surface analytical techniques were used in order to obtain complementary information to fully characterize such complex systems. X-ray Photoelectron Spectroscopy was used as the main technique to determine the surface composition of the coating. The analysis of the core level peaks of the elements provides additional information about the functional groups present on the surface. A mixture of Ce (III) and Ce (IV) was found in the coating and their proportion was calculated at different depths. The analysis of the O 1s core level peak revealed a triple structure whose origin will be discussed. To support the results obtained, electron stimulated desorption was performed. The study was completed with Auger electron spectroscopy and Raman spectroscopy, both techniques having different surface sensitivities. From all these results, it is derived that incomplete electrochemical reactions occurred during the growth of the coatings. This led to rather complex compositions, in which defective cerium oxides are the major species. In addition, hydroxides, carbonates and nitrates are also present, together with adsorbed water.

  7. Growth of monodisperse nanocrystals of cerium oxide during synthesis and annealing

    Energy Technology Data Exchange (ETDEWEB)

    Ghosh, Swapankumar, E-mail: swapankumar.ghosh2@mail.dcu.ie; Divya, Damodaran [National Institute for Interdisciplinary Science and Technology (NIIST), Council of Scientific and Industrial Research (CSIR) (India); Remani, Kottayilpadi C. [Sree Neelakanda Government Sanskrit College, Department of Chemistry (India); Sreeremya, Thadathil S. [National Institute for Interdisciplinary Science and Technology (NIIST), Council of Scientific and Industrial Research (CSIR) (India)

    2010-06-15

    Monodisperse cerium oxide nanocrystals have been successfully synthesised using simple ammonia precipitation technique from cerium(III) nitrate solution at different temperatures in the range 35-80 {sup o}C. The activation energy for growth of CeO{sub 2} nanocrystals during the precipitation is calculated as 11.54 kJ/mol using Arrhenius plot. Average crystal diameter was obtained from XRD analysis, HR-TEM and light scattering (PCS). The analysis of size data from HR-TEM images and PCS clearly indicated the formation of highly crystalline CeO{sub 2} particles in narrow size range. CeO{sub 2} nanocrystals precipitated at 35 {sup o}C were further annealed at temperatures in the range 300-700 {sup o}C. The activation energy for crystal growth during annealing is also calculated and is close to the reported values. An effort is made to predict the mechanism of crystal growth during the precipitation and annealing.

  8. Lanthanum, cerium, praseodymium, and neodymium metals and their interaction with oxygen studied by photoelectron spectroscopy

    International Nuclear Information System (INIS)

    Clean films of La, Ce, Pr, and Nd, prepared by in situ evaporation have been investigated by photoelectron spectroscopy. Different light sources He I (hv = 21.2 eV), He II (hv = 40.8 eV) and Mg Kα (hv = 1253.6 eV) have been used for the electron excitation in order to characterize the metals. Measurements have been performed after exposing the clean metals to various amounts of oxygen. From the vanishing of the emission from the sd conduction band upon exposure the conclusion is drawn that an oxide layer thicker than the probing depth (20 A) is formed on all four metals and that the oxide (at room temperature) has the form: Me2O3, Me=La, Ce, Pr, Nd. The tetravalent cerium oxide is obtained when the film is heated to about 6000C during oxygen exposure. The interaction with oxygen is also characterized by recording the oxygen 1s level and some metal core levels (Me 3d, 4d and 4p). The results from the pure metals and from the metal oxides give further experimental evidence for a 4f level binding energy of 1.9 eV in γ-cerium. (Auth.)

  9. Cerium oxide nanoparticles stimulate proliferation of primary mouse embryonic fibroblasts in vitro.

    Science.gov (United States)

    Popov, Anton L; Popova, Nelly R; Selezneva, Irina I; Akkizov, Azamat Y; Ivanov, Vladimir K

    2016-11-01

    The increasing application of cell therapy technologies in the treatment of various diseases requires the development of new effective methods for culturing primary cells. The major limitation for the efficient use of autologous cell material is the low rate of cell proliferation. Successful cell therapy requires sufficient amounts of cell material over a short period of time with the preservation of their differentiation and proliferative potential. In this regard, the development of novel, highly efficient stimulators of proliferative activity in stem cells is a truly urgent task. In this paper we have demonstrated that citrate-stabilized cerium oxide nanoparticles (nanoceria) enhance the proliferative activity of primary mouse embryonic fibroblasts in vitro. Cerium oxide nanoparticles stimulate cell proliferation in a wide range of concentrations (10(-3)М-10(-9)M) through reduction of intracellular levels of reactive oxygen species (ROS) during the lag phase of cell growth and by modulating the expression level of the major antioxidant enzymes. We found the optimal concentration of nanoceria, which provides the greatest acceleration of cell proliferation in vitro, while maintaining the levels of intracellular ROS and mRNA of antioxidant enzymes in the physiological range. Our results confirm that nanocrystalline ceria can be considered as a basis for effective and inexpensive supplements in cell culturing. PMID:27524035

  10. Stacking fault energetics of α - and γ -cerium investigated with ab initio calculations

    Science.gov (United States)

    Östlin, A.; Di Marco, I.; Locht, I. L. M.; Lashley, J. C.; Vitos, L.

    2016-03-01

    At ambient pressure the element cerium shows a metastable (t1 /2˜40 years) double-hexagonal close-packed β phase that is positioned between two cubic phases, γ and α . With modest pressure the β phase can be suppressed, and a volume contraction (17%) occurs between the γ and the α phases as the temperature is varied. This phenomenon has been linked to subtle alterations in the 4 f band. In order to rationalize the presence of the metastable β phase, and its position in the phase diagram, we have computed the stacking fault formation energies of the cubic phases of cerium using an axial interaction model. This model links the total energy differences between hexagonal closed-packed stacking sequences and stacking fault energetics. Total energies are calculated by density functional theory and by dynamical mean-field theory merged with density functional theory. It is found that there is a large difference in the stacking fault energies between the α and the γ phase. The β -phase energy is nearly degenerate with the γ phase, consistent with previous third-law calorimetry results, and dislocation dynamics explain the pressure and temperature hysteretic effects.

  11. Thermodynamic Studies of the Phase Relationships of Nonstoichiometric Cerium Oxides at Higher Temperatures

    DEFF Research Database (Denmark)

    Sørensen, Ole Toft

    1976-01-01

    Partial molar thermodynamic quantities for oxygen in nonstoichiometric cerium oxides were determined by thermogravimetric analysis in CO/CO2 mixtures in the temperature range 900–1400°C. Under these conditions compositions within the range 2.00 greater-or-equal, slanted O/M greater-or-equal, slan......Partial molar thermodynamic quantities for oxygen in nonstoichiometric cerium oxides were determined by thermogravimetric analysis in CO/CO2 mixtures in the temperature range 900–1400°C. Under these conditions compositions within the range 2.00 greater-or-equal, slanted O/M greater......-or-equal, slanted not, vert, similar1.75 could be obtained. A detailed analysis of the data shows that the α′-phase region in the phase diagram, previously described as a grossly nonstoichiometric phase, can be divided into several subregions each consisting of an apparent nonstoichiometric single phase. The finer...... details of the thermodynamic data, however, suggest that some of these subregions can be further split into ordered intermediate phases with compositions following the series MnO2n−2. Supplementary high-temperature X-ray diffraction studies under vacuum were made at temperatures up to 855°C. At the higher...

  12. Complete Oxidation of Methane over Palladium Supported on Alumina Modified with Calcium, Lanthanum, and Cerium Ions

    Institute of Scientific and Technical Information of China (English)

    Beata Stasinska; Wojciech Gac; Theophilos Ioannides; Andrzej Machocki

    2007-01-01

    The activity and thermal stability of Pd/Al2O3 and Pd/(Al2O3+MOx) (M=Ca, La, Ce) palladium catalysts in the reaction of complete oxidation of methane are presented in this study. The catalyst supports were prepared by sol-gel method and they were dried either conventionally or with supercritical carbon dioxide. Then they were impregnated with palladium nitrate solution. The catalysts with unmodified alumina had a high surface area. The activity and thermal stability of the alumina-supported catalyst was also very high. The introduction of calcium, lanthanum, or cerium oxide into alumina support caused a decrease of the surface area in the way dependent on the support precursor drying method. These modifiers decreased the activity of palladium catalysts, and they required higher temperatures for the complete oxidation of methane than unmodified Pd/Al2O3. The improvement of the palladium activity by lanthanum and cerium support modifier was observed only at low temperatures of the reaction.

  13. Magnetic studies of GaN nanoceramics doped with 1% of cerium

    Institute of Scientific and Technical Information of China (English)

    K. Oganisian; P. Gluchowski; W. Strek

    2011-01-01

    The magnetization measurements of gallium intride nanoceramics doped with 1% of cerium and sintered under various pressures were reported.It was found that GaN nanoceramics doped with cerium showed paramagnetic behavior in the wide temperature range.Nanoceramics of GaN with 1% of Ce (as undoped GaN) was diamagnetic one,but under certain temperature the paramagnetic properties started to dominate.This crossover temperature was nonlinearly dependent on the pressure applied during the sintering.The fitting of molar magnetic susceptibility allowed to estimate the Curie temperature,Curie constant and diamagnetic part of susceptibility.As it was found,all the samples showed the antiferromagnetic ordering with θp≈-1 K.Also,the effective magnetic moment was estimated for all of the samples.As a result,magnetic moments in terms of Ce ion were notably larger in comparison with those obtained within the Russell-Saunders coupling model.We suggested that it was the strong influence of amorphous shell which was rising with the pressure applied during the sintering.Finally,we presented dependences of magnetization as a function of applied field.All the samples manifested weak ferromagnetism at high temperatures and paramagnetic behavior in low temperature region.

  14. Visible Light Induced Photocatalysis of Cerium Ion Modified Titania Sol and Nanocrystallites

    Institute of Scientific and Technical Information of China (English)

    Yibing XIE; Chunwei YUAN

    2004-01-01

    The cerium ion(Ce4+) doped titania sol and nanocrystallites were prepared by chemical coprecipitation-peptization and hydrothermal synthesis methods, respectively. The X-ray diffraction pattern shows that Ce4+-TiO2 xerogel powder has semicrystalline structure and thermal sintering sample has crystalline structure. Ce4+-TiO2 nanocrystallites are composed of the major anatase phase titania (88.82 wt pct) and a small amount of crystalline cerium titanate.AFM micrograph shows that primary particle size of well-dispersed ultrafine sol particles is below 15 nm in diameter.The particle sizes are 30 nm for xerogel sample and 70 nm for nanocrystallites sample, which is different from the estimated values (2.41 nm and 4.53 nm) by XRD Scherrer's formula. The difference is mainly due to aggregation of nanocrystallites. The experimental results exhibit that photocatalysts of Ce4+-TiO2 sol and nanocrystallites have the ability to photodegrade reactive brilliant red dye (X-3B) under visible light irradiation with the ion-TiO2/VIS/dye system. Moreover, Ce4+ doped titania sol has shown higher efficiency than the nanocrystallites sample in respect of potocatalytic activity. Meanwhile, dye photodegradation mechanisms are proposed to different photocatalytic reaction systems, which are dye photosensitization, ion-dye photosensitization and interband photocatalysis & dye photosensitization with respect to TiO2 nanocrystallites, Ce4+-TiO2 sol and Ce4+-TiO2 nanocrystallites system.

  15. Yttrium and lanthanum recovery from low cerium carbonate, yttrium carbonate and yttrium concentrate

    International Nuclear Information System (INIS)

    In this work, separation, enrichment and purification of lanthanum and yttrium were performed using as raw material a commercial low cerium rare earth concentrate named LCC (low cerium carbonate), an yttrium concentrate named 'yttrium carbonate', and a third concentrated known as 'yttrium earths oxide. The first two were industrially produced by the late NUCLEMON - NUCLEBRAS de Monazita e Associados Ltda, using Brazilian monazite. The 'yttrium earths oxide' come from a process for preparation of lanthanum during the course of the experimental work for the present thesis. The following techniques were used: fractional precipitation with urea; fractional leaching of the LCC using ammonium carbonate; precipitation of rare earth peroxycarbonates starting from the rare earth complex carbonates. Once prepared the enriched rare earth fractions the same were refined using the ion exchange chromatography with strong cationic resin without the use of retention ion and elution using the ammonium salt of ethylenediaminetetraacetic acid. With the association of the above mentioned techniques were obtained pure oxides of yttrium (>97,7%), lanthanum (99,9%), gadolinium (96,6%) and samarium (99,9%). The process here developed has technical and economic viability for the installation of a large scale unity. (author)

  16. A mixed acid based vanadium-cerium redox flow battery with a zero-gap serpentine architecture

    Science.gov (United States)

    Leung, P. K.; Mohamed, M. R.; Shah, A. A.; Xu, Q.; Conde-Duran, M. B.

    2015-01-01

    This paper presents the performance of a vanadium-cerium redox flow battery using conventional and zero-gap serpentine architectures. Mixed-acid solutions based on methanesulfonate-sulfate anions (molar ratio 3:1) are used to enhance the solubilities of the vanadium (>2.0 mol dm-3) and cerium species (>0.8 mol dm-3), thus achieving an energy density (c.a. 28 Wh dm-3) comparable to that of conventional all-vanadium redox flow batteries (20-30 Wh dm-3). Electrochemical studies, including cyclic voltammetry and galvanostatic cycling, show that both vanadium and cerium active species are suitable for energy storage applications in these electrolytes. To take advantage of the high open-circuit voltage (1.78 V), improved mass transport and reduced internal resistance are facilitated by the use of zero-gap flow field architecture, which yields a power density output of the battery of up to 370 mW cm-2 at a state-of-charge of 50%. In a charge-discharge cycle at 200 mA cm-2, the vanadium-cerium redox flow battery with the zero-gap architecture is observed to discharge at a cell voltage of c.a. 1.35 V with a coulombic efficiency of up to 78%.

  17. Corrosion behaviour of sol-gel coatings doped with cerium salts on 2024-T3 aluminum alloy

    Energy Technology Data Exchange (ETDEWEB)

    Shi Hongwei; Liu Fuchun [State Key Laboratory for Corrosion and Protection, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016 (China); Han Enhou, E-mail: ehhan@imr.ac.cn [State Key Laboratory for Corrosion and Protection, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016 (China)

    2010-11-01

    The corrosion behaviour of the sol-gel coatings doped with cerium chloride or cerium nitrate on 2024-T3 aluminum alloy was investigated by using electrochemical impedance spectroscopy (EIS) and immersion tests. The sol-gel matrix was obtained through hydrolysis, condensation of 3-glycidoxypropyltrimethoxysilane (GPTMS) and tetramethoxysilane (TMOS), using diethylentriamine as curing agent. The results indicated that cerium nitrate with concentration of 1 x 10{sup -3} mol L{sup -1} in the silane solution was excellent on self-healing for the sol-gel coating, while cerium chloride had no obvious effect. This result suggested that the introduction of Cl{sup -} promoted the under-film pitting of 2024-T3 substrate. It was found that Ce(OH){sub 3} and Ce(OH){sub 2}{sup 2+} simultaneously existed in the silane solution by X-ray diffraction (XRD) analysis. Ce(OH){sub 2}{sup 2+} transformed to CeO{sub 2} due to high-temperature curing of sol-gel matrix demonstrated by X-ray photoelectron spectroscopy (XPS) analysis. Therefore, it can be considered that Ce(OH){sub 3} and CeO{sub 2} played inhibition roles in the corrosion process of the sol-gel coatings.

  18. Cerium dioxide as a new reactive sorbent for fast degradation of parathion methyl and some other organophosphates

    Czech Academy of Sciences Publication Activity Database

    Janos, P.; Kuráň, P.; Kormunda, M.; Štengl, Václav; Matys Grygar, Tomáš; Došek, M.; Šťastný, M.; Ederer, J.; Pilařová, V.; Vrtoch, L.

    2014-01-01

    Roč. 32, č. 4 (2014), s. 360-370. ISSN 1002-0721 Institutional support: RVO:61388980 Keywords : cerium dioxide * carbonate precursor * lanthanides * organophosphate pesticide * parathion methyl * chemical warfare agents Subject RIV: CA - Inorganic Chemistry Impact factor: 1.261, year: 2014

  19. Germination and early plant development of ten plant species exposed to titanium dioxide and cerium oxide nanoparticles

    Science.gov (United States)

    Ten agronomic plant species were exposed to different concentrations of nano titanium dioxide (nTiO2) or nano cerium oxide (nCeO2) (0, 250, 500 and 1000 mg/L) to examine potential effects on germination and early seedling development. We modified a standard test protocol develop...

  20. Effect of cerium ion implantation on the oxidation behavior of zircaloy-4 at 500 degree sign C

    CERN Document Server

    Chen, X W; Yu, H R; Zhou, Q G; Chen, B S

    2002-01-01

    In order to investigate the oxidation behavior changes of zircaloy-4 induced by cerium ion implantation using a MEVVA source at an energy of 40 keV with a dose range from 1x10 sup 1 sup 6 to 1x10 sup 1 sup 7 ions/cm sup 2 at the maximum temperature of 130 degree sign C, weight gain curves of the different specimens including as-received zircaloy-4 and cerium-implanted zircaloy-4 were measured after oxidation in air at 500 degree sign C for 100 min. It was obviously found that a significant improvement was achieved in the oxidation behavior of cerium ion implanted zircaloy-4 compared with that of the as-received zircaloy-4. The depth profile of the element composition in the surface region of the samples was obtained by Auger electron spectroscopy, and the valence of the oxides in the scale was analyzed by X-ray photoemission spectroscopy. Glancing angle X-ray diffraction employed to examine the phase transformation in the oxide films showed that the addition of cerium transformed the phase from monoclinic zir...

  1. Effect of rare element cerium on the morphology and corrosion resistance of electro-less Ni-P coatings

    Directory of Open Access Journals (Sweden)

    Fu Chuan-qi

    2015-01-01

    Full Text Available This paper reports an experimental study on the microstructure and corrosion resistance of electro-less Ni-P coatings with increasing content of the rare element cerium (Ce. Surface morphology and the composition of the electro-less Ni-P coatings were studied by scanning electron microscope (SEM, X-ray energy dispersed analysis (EDS and X-ray diffraction analysis (XRD. Hardness and Adhesive force are researched by a HX-200 Vickers diamond indenter micro-hardness tester. Furthermore, we study the adhesive force by using the Revetest scratch tester. We get the possession of Ce amorphous Ni-P coatings which has excellent properties in anti-corrosion. The effect of the rare element cerium concentration on corrosion resistance of the coatings was evaluated in the groundwater immersion test and porosity test, respectively. The results indicated that added little the rare element cerium into the plating bath increased the phosphorus content of the coatings, decreased the corrosion rates, it also decreases the porosity of the amorphous Ni-P coatings. The lowest corrosion rates of the amorphous Ni-P coatings in groundwater immersion test is 4.1 um · h-1, at the rare element cerium concentration of 0.12g · L-1.

  2. Compound odontoma

    Directory of Open Access Journals (Sweden)

    Monica Yadav

    2012-01-01

    Full Text Available Odontomas have been extensively reported in the dental literature, and the term refers to tumors of odontogenic origin. Though the exact etiology is still unknown, the postulated causes include: local trauma, infection, inheritance and genetic mutation. The majority of the lesions are asymptomatic; however, may be accompanied with pain and swelling as secondary complaints in some cases. Here, we report a case of a compound odontome in a 14 year old patient.

  3. Magnesium compounds

    Science.gov (United States)

    Kramer, D.A.

    2006-01-01

    In 2005, seawater and natural brines accounted for 51% of US magnesium compounds production. World magnesia production was estimated to be 14.5 Mt. Most of the production came from China, North Korea, Russia and Turkey. Although no specific production figures are available, Japan and the United States are estimated to account for almost one-half of the world's capacity from seawater and brines.

  4. catena-Poly[[tetrakis(hexamethylphosphoramide-κObis(nitrato-κ2O,O′cerium(III] [silver(I-di-μ-sulfido-tungstate(VI-di-μ-sulfido

    Directory of Open Access Journals (Sweden)

    Hongyang Wei

    2010-12-01

    Full Text Available Hexamethylphosphoramide (hmp, tetrathiotungstate, silver sulfide and cerium nitrate were self-assembled to form a one-dimensional anionic [Ag4W4S16]n4n− chain in the title compound, {[Ce(NO32(C6H18N3OP4][AgWS4]}n. The asymmetric unit contains four crystallographically independent [Ce(hmp4(NO32]+ cations, which leads to a one-dimensional polymeric anionic chain having a tetravalent [W4S16Ag4] repeat unit. Each central Ce atom is coordinated by eight O atoms from two chelating nitrate and four hmp ligands, which gives rise to a distorted square-antiprismatic structure. The polymeric chain with average W—Ag—W and Ag—W—Ag bond angles of 163.75 and 151.84°, respectively, presents a distorted linear configuration. The title complex with a non-centrosymmetric structure, is analogous to the Yb, Y, Eu, Nd, La and Dy isomorphs, which exhibit centrosymmetric structures.

  5. Destruction of organic pollutants by cerium(IV) MEO process: A study on the influence of process conditions for EDTA mineralization

    International Nuclear Information System (INIS)

    The mediated electrochemical oxidation (MEO) process with cerium(IV) and nitric acid as the oxidizing medium was employed for the destruction of various model organic pollutants in continuous organic feeding mode. A near complete destruction was observed for all the organics studied. The effects of various experimental conditions were evaluated with respect to EDTA mineralization. The key parameters varied in the process were concentration of EDTA (67-268 mM), temperature (70, 80 and 95 deg. C), concentrations of Ce(IV) (0.7, 0.8 and 0.95 M), nitric acid (2, 3 and 4 M) and duration of organic addition (30 and 120 min). Under the experimental conditions of 80 deg. C and 0.95 M Ce(IV) in 3 M nitric acid, nearly 90% destruction was achieved based on CO2 production and 95% based on TOC analyses for all the organic compounds studied. The in situ regeneration of mediator ion by the electrochemical cell was found to be good during the organic destruction within the range of experimental conditions studied. In the case of long term organic feeding (120 min) the destruction was calculated after the CO2 evolution attained the steady state and under this condition the destruction efficiency was found to be 85% based on CO2 evolution

  6. Thermoluminescence and sintering of ultra-pure α alumina doped with zirconium, thorium, calcium or cerium

    International Nuclear Information System (INIS)

    Thermoluminescence is a technique of identification of the point defects that appear in a solid consecutively to its fabrication. The synthesis parameters of α-alumina that will be taken into account here are the atmosphere during thermal treatment (oxidising or reducing), and the effect of the dopants: zirconium, thorium, calcium or cerium. The aim of this work is to correlate the point defects to the reactivity of the powder, especially its sintering. The TL mechanisms of the dosimetric peak of α-alumina, around 200 deg C, were clarified: the trap is an aggregate of 2 point defects (Val-VO), and the recombination centre is Cr3+. The sensibilizing effect observed for thorium, or for cerium under reducing atmosphere, is attributed to the presence of a large emission band in the blue-green domain. Chromium is the main impurity at the origin of the E' peak (360 deg C) of α-alumina. It is acting as trap and also as recombination centre. A mechanism of transfer of energy between Cr3+ and Ti4+ is also presented in order to explain the increase of the TL intensity of the E' peak when doping by a tetravalent cation. In the case of doping by calcium, TL allows the revelation of the phase CaAl12O19. A quenching was observed for αAl2O3:Ca and αAl2O3:Ce under reducing atmosphere. It is attributed to oxygen vacancies for the doping by calcium, and to the presence of Ce3+ for the doping by cerium. The alumina prepared under reducing conditions exhibit a perturbation of kinetics during sintering, and also abnormal grain growth in doped samples. This unusual kinetic is explained by a decrease in the concentration of aluminium vacancies under reducing atmosphere, conducting indirectly to a greater segregation of Si4+ at the grain boundaries, and to the formation of a liquid phase at the surface of grains. This phenomenon is amplified in the case of doping by calcium. (authors)

  7. Computational and Experimental Study of the Thermodynamics of Uranium-Cerium Mixed Oxides

    Science.gov (United States)

    Hanken, Benjamin Edward

    The thermophysical properties of mixed oxide (MOX) fuels, and how they are influenced by the incorporation of fission products and other actinides, must be well understood for their safe use in an advanced fuel cycle. Cerium is a common plutonium surrogate in experimental studies of MOX, as it closely matches plutonium's ionic radii in the 3+ and 4+ oxidation states, and is soluble in fluorite-structured UO2. As a fission product, cerium's effects on properties of MOX are also of practical interest. To provide additional insights on structure-dependent behavior, urania solid solutions can be studied via density functional theory (DFT), although approaches beyond standard DFT are needed to properly account for the localized nature of the ƒ-electrons. In this work, DFT with Hubbard-U corrections (DFT+U) was employed to study the energetics of fluorite-structured U1-yCe yO2 mixtures. The employed computational approach makes use of a procedure which facilitates convergence of the calculations to multiple self-consistent DFT+U solutions for a given cation arrangement, corresponding to different charge states for the U and Ce ions in several prototypical cation arrangements. Results indicate a significant dependence of the structural and energetic properties of U1-yCeyO2 on the nature of both charge and cation ordering. With the effective Hubbard-U parameters that reproduce well the measured oxidation-reduction energies for urania and ceria, it was found that charge transfer between U4+ and Ce4+ ions, leading to the formation of U5+ and Ce3+, gives rise to an increase in the mixing energy in the range of 4-14 kJ/mol of the formula unit, depending on the nature of the cation ordering. In conjunction with the computational approach, high-temperature oxide-melt drop-solution calorimetry experiments were performed on eight samples spanning compositions of y = 0.119 to y = 0.815. Room temperature mixing enthalpies of U1-yCeyO2 determined from these experiments show near

  8. Cerium doped lanthanum halides: fast scintillators for medical imaging; Halogenures de lanthane dopes cerium des scintillateurs rapides pour l'imagerie medicale

    Energy Technology Data Exchange (ETDEWEB)

    Selles, O

    2006-12-15

    This work is dedicated to two recently discovered scintillating crystals: cerium doped lanthanum halides (LaCl{sub 3}:Ce{sup 3+} and LaBr{sub 3}:Ce{sup 3+}).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 Ce{sup 3+} 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)

  9. Intermetallic Compounds

    Science.gov (United States)

    Takagiwa, Y.; Matsuura, Y.; Kimura, K.

    2014-06-01

    We have focused on the binary narrow-bandgap intermetallic compounds FeGa3 and RuGa3 as thermoelectric materials. Their crystal structure is FeGa3-type (tetragonal, P42/ mnm) with 16 atoms per unit cell. Despite their simple crystal structure, their room temperature thermal conductivity is in the range 4-5-W-m-1-K-1. Both compounds have narrow-bandgaps of approximately 0.3-eV near the Fermi level. Because their Seebeck coefficients are quite large negative values in the range 350-thermoelectric materials both by adjusting the carrier concentration and by reducing the thermal conductivity. Here, we report the effects of doping on the thermoelectric properties of FeGa3 and RuGa3 as n and p-type materials. The dimensionless figure of merit, ZT, was significantly improved by substitution of Sn for Ga in FeGa3 (electron-doping) and by substitution of Zn for Ga in RuGa3 (hole-doping), mainly as a result of optimization of the electronic part, S 2 σ.

  10. Crystal structure of a Ce2Fe2Mg15 compound

    International Nuclear Information System (INIS)

    A structure of a new Ce2Fe2Mg15 ternary compound (P63/mmc sp.gr., a=1.0324(5) nm, c=1.02080(4) nm) was determined by powder methods on a DRON-4.07 automatic diffractometer. The structure of a Ce2Fe2Mg15 crystal is a new variant of the ordered Th2Ni17 type superstructure, in which cerium atoms occupy the thorium positions; magnesium atoms occupy the nickel position 6g, 12k, and 12j; and iron atoms occupy the 4f position

  11. Effect of Rare Earth Element Cerium on Mechanical Properties and Morphology of TiN Coating Prepared by Arc Ion Plating

    Institute of Scientific and Technical Information of China (English)

    黄拿灿; 胡社军; 谢光荣; 曾鹏; 汝强

    2003-01-01

    TiN coatings were deposited on polished substrates of W18Cr4V high speed steel by means of vacuum arc ion plating. The effect of cerium on adhesion between TiN coating and substrate was studied. The microstructures and composition of TiN coatings were also investigated by means of scanning electron microscope (SEM), Auger electron spectroscopy (AES), and X-ray diffraction (XRD) technique. It was found that cerium is an effective modifying agent and the addition of suitable amount of cerium to TiN coatings can produce relatively excellent properties such as micro-hardness, wear resistance, oxidation resistance and porosity. The experimental results show that the added cerium in TiN coatings makes a contribution to form the preferred direction along with a (111) or (222) close packed face, which may be one of the reasons that improves some properties mentioned above.

  12. Preparation, characterization and photocatalytic properties of cerium doped TiO.sub.2./sub. : On the effect of Ce loading on the photocatalytic reduction of carbon dioxide

    Czech Academy of Sciences Publication Activity Database

    Matějová, L.; Kočí, B.; Reli, M.; Čapek, L.; Hospodková, Alice; Peikertová, P.; Matěj, Z.; Obalová, L.; Wach, A.; Kustrowski, P.; Kotarba, A.

    152-153, JUN (2014), s. 172-183. ISSN 0926-3373 Institutional support: RVO:68378271 Keywords : cerium * titania * nanocrystalline * photocatalysis Subject RIV: CF - Physical ; Theoretical Chemistry Impact factor: 7.435, year: 2014

  13. Effects of acetic acid on microstructure and electrochemical properties of nano cerium oxide films coated on AA7020-T6 aluminum alloy

    Institute of Scientific and Technical Information of China (English)

    H. Hasannejad; T. Shahrabi; M. Aliofkhazraei

    2009-01-01

    Nano cerium oxide films were applied on AA7020-T6 aluminum alloy and the effects of acetic acid concentration on the microstructure and electrochemical properties of the coated samples were investigated by using scanning electron microscopy (SEM), X-ray diffraction (XRD), crack-flee films with well-developed grains were obtained and grain sizes of the films decreased. Elimination of cracks and decreasing grain size of the nano cerium oxide films caused corrosion resistance to increase.

  14. Study on Electrochemical Characteristics of Electroless Co-Ni-B Alloy with Cerium

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    The effects of rare earth element cerium on composition and electrochemical characteristics of electroless Co-Ni-B alloy were studied in this paper. The alloy component was analyzed using Inductively Coupled Plasma (ICP). The plating rate is was determined by electronic balance. The cathode polarization curves and cyclic voltammogram during the electroless deposition were tested by LK998Ⅱmodel electrochemical analytical system. The results show that rare earth element Ce can co-deposit with cobalt-based alloy, and with mass increase of Ce added in aqueous solution, the contents of Co, Ni, Ce in alloy increase and the content of B decreases. Ce can increase deposition rate of alloy in some range. The rare earth makes deposition potential move to positive direction and makes polarizability decrease.

  15. Effect of cerium on ignition point of AZ91D magnesium alloy

    Institute of Scientific and Technical Information of China (English)

    Zhao Hongjin; Zhang Yinghui; Kang Yonglin

    2008-01-01

    The surface and interior temperature-time curves of blocky cerium modified AZ91D magnesium alloy were measured during a non-protective heating and melting process. Two inflection points with rapid increase in temperature were found on both curves, which corresponded to the formation of "auliflower" oxide on the surface and the occurrence of flame during melting. These two temperatures are therefore defined as oxidation point and ignition point, respectively.The interior temperature-time curve is similar to that measured on the surface except for a comparable time delay. The oxidation and ignition temperatures increase with Ce content, an average increase of 33℃ and 61℃ was found when Ce addition was about 1.0 wt %. However, the increasing rate of the oxidation and ignition temperature decreases with increasing Ce content. An addition of 0.6wt% Ce is recommended for ignition-resistant AZ91 magnesium alloy.

  16. Cerium-based binary and ternary oxides in the transesterification of dimethylcarbonate with phenol.

    Science.gov (United States)

    Dibenedetto, Angela; Angelini, Antonella; di Bitonto, Luigi; De Giglio, Elvira; Cometa, Stefania; Aresta, Michele

    2014-04-01

    Diphenyl carbonate (DPC) plays a key role in phosgene-free carbonylation processes. It can be produced by transesterification of dimethyl carbonate (DMC) with phenol in the presence of catalysts. Methyl phenyl carbonate (MPC) is first produced that is then converted into DPC by either disproportionation or further transesterification with phenol. Cerium-based bimetallic oxides (with the heterometal being niobium, iron, palladium, or aluminum) are used as catalysts in the transesterification of DMC to synthesize MPC. The catalytic activity is affected by the type and concentration of the heterometal. XPS, IR and elementary analyses are employed to characterize the new catalysts. Differently from pure oxides, the mixed oxides produce a significant increase of the conversion and selectivity towards MPC. PMID:24616260

  17. Fabrication of condensate microdrop self-propelling porous films of cerium oxide nanoparticles on copper surfaces.

    Science.gov (United States)

    Luo, Yuting; Li, Juan; Zhu, Jie; Zhao, Ye; Gao, Xuefeng

    2015-04-13

    Condensate microdrop self-propelling (CMDSP) surfaces have attracted intensive interest. However, it is still challenging to form metal-based CMDSP surfaces. We design and fabricate a type of copper-based CMDSP porous nanoparticle film. An electrodeposition method based on control over the preferential crystal growth of isotropic nanoparticles and synergistic utilization of tiny hydrogen bubbles as pore-making templates is adopted for the in situ growth of cerium oxide porous nanoparticle films on copper surfaces. After characterizing their microscopic morphology, crystal structure and surface chemistry, we explore their CMDSP properties. The nanostructure can realize the efficient ejection of condensate microdrops with sizes below 50 μm. PMID:25693502

  18. Nanoscale Hybrid Langmuir-Blodgett Films Based on Cerium-Substituted Heteropolymolybdate and Polyquinoline

    Institute of Scientific and Technical Information of China (English)

    王峥; 柳士忠; 杜祖亮; 胡振纲; 张洪杰

    2003-01-01

    Nanoscale hybrid organic/inorganic Langmuir-Blodgett films of cerium-substituted heteropolymolybdates(Ce-HPMo) and π-conjugated macromolecule poly(1,2-dihydro-2,2,4-trimethyl)quinoline(PQ) were obtained with auxiliary film-forming material stearic acid(SA) or octadecylamine(ODA). The surface pressure-area isotherms illuminate the formation of the hybrid LB films of PQ/ODA/Ce-HPMo and P Q/SA/Ce-HPMo. The different film-forming mechanism was discussed when the different auxiliary film-forming materials were used in the system. The absorption spectra indicate that the molecules of PQ and Ce-HPMo are incorporated into the LB films. Tapping-mode AFM image reveals a granular surface texture of nanosized Ce-substituted heteropolymolybdate. STM image shows that the conductivity is greatly improved after Ce-substituted heteropolymolybdates are incorporated in the films.

  19. Extraction of Uranium and Cerium mixture with liquid membrane emulsion process using Tributylphosphate extractant

    International Nuclear Information System (INIS)

    As a membrane a mixture of surfactant (span-80), Tributylphosphate in kerosene and sodium carbonate was used. The feeder was a mixture of uranium and cerium solution with 418.88 ppm U and 101.81 ppm Ce concentration in nitrate acid. The variables investigated were % surfactant (1-8 %) percentage, rotary speed for membrane making (2,500-10,000 rpm) and the acidity of feeder (0.5-3 M). The experiment result were that the optimal concentration of surfactant 5 %, rotary speed 7,500 rpm and efficiency extraction (efeks-U = 23.65 %, efeks-Ce = 7.09 %) at 0.5 M nitric acid and the efficiency stripping (efstripp-U = 5.06 %, efstripp-Ce = 99.91 %) at 0.5 M nitric acid

  20. Cerium-activated sol–gel silica glasses for radiation dosimetry in harsh environment

    Science.gov (United States)

    El Hamzaoui, Hicham; Capoen, Bruno; Helou, Nissrine Al; Bouwmans, Géraud; Ouerdane, Youcef; Boukenter, Aziz; Girard, Sylvain; Marcandella, Claude; Duhamel, Olivier; Chadeyron, Geneviève; Mahiou, Rachid; Bouazaoui, Mohamed

    2016-04-01

    Cerium-doped silica glass has been prepared for ionizing radiation dosimetry applications, using the sol–gel route and densification under different atmospheres. In comparison with the glass densified under air atmosphere, the one obtained after sintering the xerogel under helium gas presents improved optical properties, with an enhancement of the photoluminescence quantum yield up to 33%, which is attributed to a higher Ce3+ ions concentration. Such a glassy rod has been jacketed in a quartz tube and then drawn at high temperature to a cane, which has been used as active material in a fibered remote x-ray radiation dosimeter. The sample exhibited a reversible linear radioluminescence intensity response versus the dose rate up to 30 Gy s‑1. These results confirm the potentialities of this material for in vivo or high rate dose remote dosimetry measurements.

  1. Diffusion of Barium, Strontium and Cerium in Various Grades of Reactor Graphite

    International Nuclear Information System (INIS)

    Experiments designed to study the diffusion of barium, strontium and cerium in various grades of graphite of interest to the Dragon reactor project will be described. In these experiments specimens of the graphite are immersed in the vapour of the fission product metal under controlled conditions of temperature and pressure for known periods of time. After appropriate grinding and polishing, the distribution of the solute metal in the specimen is determined by means of an electron microprobe. The electron microprobe recordings are then interpreted to obtain apparent values of the diffusion coefficients and their dependence upon temperature. The results indicate that migration occurs primarily via defects in the graphite structure, with only a negligible contribution from in-grain diffusion. The significance of the results is discussed, with particular reference to the differences in behaviour encountered between various grades of graphite. (author)

  2. Redox-active cerium oxide nanoparticles protect human dermal fibroblasts from PQ-induced damage

    Directory of Open Access Journals (Sweden)

    Claudia von Montfort

    2015-04-01

    Full Text Available Recently, it has been published that cerium (Ce oxide nanoparticles (CNP; nanoceria are able to downregulate tumor invasion in cancer cell lines. Redox-active CNP exhibit both selective pro-oxidative and antioxidative properties, the first being responsible for impairment of tumor growth and invasion. A non-toxic and even protective effect of CNP in human dermal fibroblasts (HDF has already been observed. However, the effect on important parameters such as cell death, proliferation and redox state of the cells needs further clarification. Here, we present that nanoceria prevent HDF from reactive oxygen species (ROS-induced cell death and stimulate proliferation due to the antioxidative property of these particles.

  3. Valence Control of Ce Ions in Cerium-substituted Yttrium Iron Garnet

    Institute of Scientific and Technical Information of China (English)

    SONG Fengbing; LI Qiang; ZHONG Zhifeng

    2005-01-01

    Cerium-substituted yttrium iron garnet(CexY3-xFe5O12, Ce∶YIG) was prepared via coprecipitation. The structure, morphology, valence state and constituent of Ce ions were investigated respectively. X-ray powder diffraction(XRD) analysis shows that Ce∶YIG was of single cubic YIG phase. The result of X-ray photoelectron spectroscopy(XPS) indicates the Ce ions in Ce∶YIG were in the state of trivalence. Scanning electron microscope(SEM) demonstrates the conglobation of Ce∶YIG particles about 0.2μm scale.The magnetic properties were studied by a vibrating sample magnetometer(VSM) and the result exhibits that substitution of Ce3+ changes the magnetic parameters of YIG. The effects of doping content of Ce ions and synthesis temperature on valence control were discussed in detail.

  4. Equiatomic cerium intermetallics CeXX' with two p elements

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-07-01

    The equiatomic CeXX' phases (X and X' = elements of the 3{sup rd}, 4{sup th}, or 5{sup th} main group) extend the large series of CeTX intermetallics (T = electron-rich transition metal). These phases crystallize with simple structure types, i.e. ZrNiAl, TiNiSi, CeScSi, α-ThSi{sub 2}, AlB{sub 2}, and GdSi{sub 2}. In contrast to the CeTX intermetallics one observes pronounced solid solutions for the CeXX' phases. The main influence on the magnetic ground states results from the absence of d electrons. All known CeXX' phases show exclusively trivalent cerium and antiferro- or ferromagnetic ordering at low temperatures. The crystal chemical details and some structure-property relationships are reviewed.

  5. Equiatomic cerium intermetallics CeXX' with two p elements

    International Nuclear Information System (INIS)

    The equiatomic CeXX' phases (X and X' = elements of the 3rd, 4th, or 5th main group) extend the large series of CeTX intermetallics (T = electron-rich transition metal). These phases crystallize with simple structure types, i.e. ZrNiAl, TiNiSi, CeScSi, α-ThSi2, AlB2, and GdSi2. In contrast to the CeTX intermetallics one observes pronounced solid solutions for the CeXX' phases. The main influence on the magnetic ground states results from the absence of d electrons. All known CeXX' phases show exclusively trivalent cerium and antiferro- or ferromagnetic ordering at low temperatures. The crystal chemical details and some structure-property relationships are reviewed.

  6. Investigation of the Carbon Monoxide Gas Sensing Characteristics of Tin Oxide Mixed Cerium Oxide Thin Films

    Directory of Open Access Journals (Sweden)

    Muhammad B. Haider

    2012-02-01

    Full Text Available Thin films of tin oxide mixed cerium oxide were grown on unheated substrates by physical vapor deposition. The films were annealed in air at 500 °C for two hours, and were characterized using X-ray photoelectron spectroscopy, atomic force microscopy and optical spectrophotometry. X-ray photoelectron spectroscopy and atomic force microscopy results reveal that the films were highly porous and porosity of our films was found to be in the range of 11.6–21.7%. The films were investigated for the detection of carbon monoxide, and were found to be highly sensitive. We found that 430 °C was the optimum operating temperature for sensing CO gas at concentrations as low as 5 ppm. Our sensors exhibited fast response and recovery times of 26 s and 30 s, respectively.

  7. Synthesis and properties of solid complexes of lanthanum, cerium. neodymium and erbium with N-phosphonomethylglicyne

    International Nuclear Information System (INIS)

    Water soluble complexes of lanthanum(III), cerium(III), neodymium(III) and erbium(III) with N-phosphonomethylglycine (glyphosate, NMPG) of the general formulae: LaC3H5NO5P·H2O, CeC3H5NO5P·H2O, NdC3H5NO5P·1.5H2O, ErC3H5NO5P·2H2O were synthesized. The solubility in water was determined. Thermal, diffractometric and IR spectrophotometric analyses were carried out. It was found that the lanthanide ions are bonded to N-phosphonmethylglycine through the oxygen atoms of the carboxylic and phosphonate groups and the nitrogen atom of the amine group. The final products of thermal decomposition at 900 oC were determined. (author)

  8. Distribution of Cerium Ion in Cordierite Ceramics and Its Effect on Structure of Cordierite Crystal

    Institute of Scientific and Technical Information of China (English)

    Shi Zhiming

    2004-01-01

    Cerium addition plays an important role in sintering, transformation and phasicochemical properties of cordierite ceramics. The present work aims at studying the distribution of Ce4+ in cordierite ceramics and its effect on the structure of cordierite crystal by means of differential thermal analysis (DTA), X-ray diffraction (XRD) and scanning electronic microscope (SEM) so as to clarify the behavior of Ce4+. Results show that Ce4+ can exist in two forms of CeO2 particles and solid solution in Ce4+ -modified cordierite ceramics by the sol-gel method. The CeO2 particles separately distribute in the cordierite matrix. Ce4+ dissolves little into cordierite crystal, resulting in a decrease of lattice constants ofthe crystal. This kind of distribution behavior of Ce4+ makes us to easily tailor the properties of the cordieritc ceramics.

  9. Biaxially aligned buffer layers of cerium oxide, yttria stabilized zirconia, and their bilayers

    International Nuclear Information System (INIS)

    Biaxially aligned cerium oxide (CeO2) and yttria stabilized zirconia (YSZ) films were deposited on Ni-based metal (Hastelloy C276) substrates held at room temperature using ion beam assisted (IBAD) magnetron deposition with the ion beam directed at 55 degree to the normal of the film plane. In addition, we achieved, room-temperature epitaxial growth of CeO2 by bias sputtering to form biaxially aligned CeO2/YSZ bilayers. The crystalline structure and in-plane orientation of films was investigated by x-ray diffraction techniques. Both the IBAD CeO2 and YSZ films, and the CeO2/YSZ bilayers have a (111) pole in the ion beam direction. copyright 1997 American Institute of Physics

  10. Biaxially aligned buffer layers of cerium oxide, yttria stabilized zirconia, and their bilayers

    Science.gov (United States)

    Gnanarajan, S.; Katsaros, A.; Savvides, N.

    1997-05-01

    Biaxially aligned cerium oxide (CeO2) and yttria stabilized zirconia (YSZ) films were deposited on Ni-based metal (Hastelloy C276) substrates held at room temperature using ion beam assisted (IBAD) magnetron deposition with the ion beam directed at 55° to the normal of the film plane. In addition, we achieved, room-temperature epitaxial growth of CeO2 by bias sputtering to form biaxially aligned CeO2/YSZ bilayers. The crystalline structure and in-plane orientation of films was investigated by x-ray diffraction techniques. Both the IBAD CeO2 and YSZ films, and the CeO2/YSZ bilayers have a (111) pole in the ion beam direction.

  11. Structural Characteristics of Cerium Oxide Nanocrystals Prepared by the Microemulsion Method

    Institute of Scientific and Technical Information of China (English)

    J.Zhang; X.Ju; Z.Y.Wu; T.Liu; T.D.Hu; Y.N.Xie

    2001-01-01

    The aim of this work is to investigate the microstructure development of erium oxide nanocrystal,prepared by the microemulsion process,as a function of annealing temperature in air.Combined with the HRTEM and the thermogravimetric-differential thermal analysis in air.Combined withthe HRTEm and the thremogravimetric-differential thermal analysis(TG-DTA),the XRD patterns reveal that the sample annealed at 623 K is amorphous,and the formation of cerium oxide nanocrystal occurs above 773 K.The local structural and electronic properties in the nanocrystallization process are probed by X-ray absorption spectra (XAS) at the Ce L3 edge.It is found that the phase structure changes from triclinic to cubic (CeO2),and the electroic structure changes from Ce3 to Ce4 upon increasing the annealing temperature.

  12. Compound odontoma

    Directory of Open Access Journals (Sweden)

    José Marcelo Vargas Pinto

    2008-01-01

    Full Text Available Odontomas are the most common types of odontogenic tumors, as they are considered more as a developmental anomaly (hamartoma than as a true neoplasia. The aim of the present study is to describe a clinical case of compound odontoma, analyzing its most commonsigns, its region of location, the decade of life and patient’s gender, disorders that may occur as well as the treatment proposed. In order to attain this objective, the method was description of the present clinical case and bibliographic revision, arriving at the result that the treatment for this type of lesion invariably is surgical removal (enucleation and curettage and the prognosis is excellent. The surgical result was followed up in the post-operative period by radiographic exam, and it was possible to conclude that there was complete cicatrization and tissue repair.

  13. Potential of using cerium oxide nanoparticles for protecting healthy tissue during accelerated partial breast irradiation (APBI).

    Science.gov (United States)

    Ouyang, Zi; Mainali, Madan Kumar; Sinha, Neeharika; Strack, Guinevere; Altundal, Yucel; Hao, Yao; Winningham, Thomas Andrew; Sajo, Erno; Celli, Jonathan; Ngwa, Wilfred

    2016-04-01

    The purpose of this study is to investigate the feasibility of using cerium oxide nanoparticles (CONPs) as radical scavengers during accelerated partial breast irradiation (APBI) to protect normal tissue. We hypothesize that CONPs can be slowly released from the routinely used APBI balloon applicators-via a degradable coating-and protect the normal tissue on the border of the lumpectomy cavity over the duration of APBI. To assess the feasibility of this approach, we analytically calculated the initial concentration of CONPs required to protect normal breast tissue from reactive oxygen species (ROS) and the time required for the particles to diffuse to various distances from the lumpectomy wall. Given that cerium has a high atomic number, we took into account the possible inadvertent dose enhancement that could occur due to the photoelectric interactions with radiotherapy photons. To protect against a typical MammoSite treatment fraction of 3.4Gy, 5ng·g(-1) of CONPs is required to scavenge hydroxyl radicals and hydrogen peroxide. Using 2nm sized NPs, with an initial concentration of 1mg·g(-1), we found that 2-10days of diffusion is required to obtain desired concentrations of CONPs in regions 1-2cm away from the lumpectomy wall. The resultant dose enhancement factor (DEF) is less than 1.01 under such conditions. Our results predict that CONPs can be employed for radioprotection during APBI using a new design in which balloon applicators are coated with the NPs for sustained/controlled in-situ release from within the lumpectomy cavity. PMID:27053452

  14. Decomposition processes and structural transformations of cerium propionate into nanocrystalline ceria at different oxygen partial pressures

    International Nuclear Information System (INIS)

    The structural transformations that occur when thermal treatments turn cerium propionate into nanocrystalline ceria have been analysed with thermoanalytical techniques (TG, DTA and MS) and with structural and magnetic characterization (HRTEM, SQUID and XRD) of the final and intermediate products. Attention has been paid to what occurs during the decomposition of propionate and how the process is affected by the furnace atmosphere (oxidizing or inert). In an oxidizing atmosphere, the decomposition of cerium propionate is triggered by the oxidation of Ce3+ to Ce4+. This reaction entails the loss of large unoxidized propionate fragments of the propionate ligands. As decomposition proceeds, the carbonaceous residue makes the oxygen transport inside the material more difficult and decomposition becomes diffusion limited. At this point, extensive oxidation of the residue begins until it is completely removed. Crystallization of CeO2 occurs simultaneously with decomposition. In these conditions, crystalline nanoparticles (diameter of 3–5 nm) can be obtained at a temperature as low as 300 °C. In an inert atmosphere, decomposition occurs in three steps. During the first step, one of the three propionate ligands is lost, with little oxidation of Ce3+, and is substituted by a hydroxyl group. The second step entails the loss of the remaining ligands with a substantial oxidation of Ce3+ to Ce4+. After this step, the intermediate product is, proposed as, a mixture of amorphous Ce(OH)3 and Ce(OH)4. Finally, the third step leads to conversion of the Ce hydroxide into crystalline CeO2. In an inert atmosphere, the process is less reproducible than in air and a carbonaceous residue remains in the product.

  15. Air, aqueous and thermal stabilities of Ce3+ ions in cerium oxide nanoparticle layers with substrates

    KAUST Repository

    Naganuma, Tamaki

    2014-01-01

    Abundant oxygen vacancies coexisting with Ce3+ ions in fluorite cerium oxide nanoparticles (CNPs) have the potential to enhance catalytic ability, but the ratio of unstable Ce3+ ions in CNPs is typically low. Our recent work, however, demonstrated that the abundant Ce3+ ions created in cerium oxide nanoparticle layers (CNPLs) by Ar ion irradiation were stable in air at room temperature. Ce valence states in CNPs correlate with the catalytic ability that involves redox reactions between Ce3+ and Ce4+ ions in given application environments (e.g. high temperature in carbon monoxide gas conversion and immersion conditions in biomedical applications). To better understand the mechanism by which Ce3+ ions achieve stability in CNPLs, we examined (i) extra-long air-stability, (ii) thermal stability up to 500 °C, and (iii) aqueous stability of Ce 3+ ions in water, buffer solution and cell culture medium. It is noteworthy that air-stability of Ce3+ ions in CNPLs persisted for more than 1 year. Thermal stability results showed that oxidation of Ce 3+ to Ce4+ occurred at 350 °C in air. Highly concentrated Ce3+ ions in ultra-thin CNPLs slowly oxidized in water within 1 day, but stability was improved in the cell culture medium. Ce 3+ stability of CNPLs immersed in the medium was associated with phosphorus adsorption on the Ce3+ sites. This study also illuminates the potential interaction mechanisms of stable Ce3+ ions in CNPLs. These findings could be utilized to understand catalytic mechanisms of CNPs with abundant oxygen vacancies in their application environments. © The Royal Society of Chemistry 2014.

  16. Oscillator strengths, Huang-Rhys parameters, and vibrational quantum energies of cerium-doped gadolinium oxyorthosilicate

    International Nuclear Information System (INIS)

    Temperature-dependent optical absorption of cerium-doped gadolinium oxyorthosilicate (Gd2SiO5:Ce) has been measured and analyzed for impurity-ion-lattice coupling parameters and oscillator strengths. Although the spectrum consists of overlapping Ce3+ bands and Gd3+ lines, two well-resolved Ce3+ bands with 10 K maxima at 3.32 eV (peak a) and 3.61 eV (peak b) are amenable to spectral analysis. These bands, previously assigned to Ce3+ ions occupying crystallographically inequivalent substitutional sites, are characterized by Gaussian line shapes and temperature-dependent half widths that are well described by the linear model of impurity-ion-lattice coupling. Huang-Rhys [Proc. R. Soc. A 204, 404 (1950)] parameters of peaks a and b are 22.7 and 5.7, respectively, indicating strong ion-lattice coupling, with vibrational frequencies 1.83x1013 s-1 (peak a) and 5.07x1013 s-1 (peak b). Peak b centroid is approximately temperature independent, but peak a centroid shifts to higher energy with increasing temperature. This dependence is adequately described by including higher-order coupling terms in the ion-lattice interaction, although crystal-field contributions cannot be excluded. Absorption band oscillator strengths, f, are calculated from Smakula's [Z. Phys. 59, 603 (1930)] formula and knowledge of cerium concentration for the two inequivalent sites. In the interval 10-300 K, peak a f values range from (9.8 to 26.8)x10-4 and peak b f values vary from (7.8 to 5.8)x10-3. From the known correlation between oscillator strength and metal-ion-ligand separation, we identify peaks a and b as the seven- and nine-oxygen-coordinated sites, respectively. (c) 2000 American Institute of Physics

  17. Luminescence spectroscopy of scintillating glasses doped with Tb3+/Ce3+ with different concentrations of cerium under photo- and electron excitation

    International Nuclear Information System (INIS)

    The luminescence of Li2O–B2O3–P2O5–CaF2 scintillation glass doped Tb3+, Ce3+ under electron beam excitation are investigated. Changing the cerium concentration of 0.2–1 wt% leads to an increase in luminescence intensity of Ce3+ and Tb3+ ions. Luminescence decay of cerium time is 30 ns and weakly depends on the ion concentration and the density of the excitation energy. The luminescence spectrum of the Tb3+ ions and excitation spectrum are dependent on the concentration of Ce3+. The radiative level of cerium ion does not participate in the process of energy transfer from the cerium to terbium. The transfer of energy between Ce3+ and Tb3+ occurs non-radiatively. - Highlights: • A series of Li2O–B2O3–P2O5–CaF2:Tb5, Ce (0.2; 0.5; 1 weight %) glasses were prepared. • Effect of cerium ion with different concentrations on absorption, photoluminescence, cathodoluminescence, decay dynamics was investigated. • The luminescence decay kinetics of cerium was investigated in detail. • The mechanism of energy transfer of lithium–phosphate–borate–fluoride glasses doped with Tb3+ and Ce3+ has been discussed

  18. Effect of calcination temperature on the crystallite growth of cerium oxide nano-powders prepared by the co-precipitation process

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Jian-Chih [Department of Orthopaedics, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan (China); Chen, Wen-Cheng [School of Dentistry, College of Dental Medicine, Kaohsiung Medical University, Kaohsiung 807, Taiwan (China); Tien, Yin-Chun [Department of Orthopaedics, Kaohsiung Medical University Hospital, Kaohsiung 807, Taiwan (China); Shih, Chi-Jen, E-mail: cjshih@kmu.edu.t [Department of Fragrance and Cosmetics Science, Kaohsiung Medical University, 100 Shi-Chuan1st Road, Kaohsiung 80708, Taiwan (China)

    2010-04-30

    Cerium oxide nanocrystallites were synthesized by a co-precipitation process at a relatively low temperature, using cerium (III) nitrate as the starting material in a water solution with pH in the range of 8-9. The 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 at temperatures from 473 to 1273 K, face-centered cubic phase crystallization was observed by XRD. The crystallite size of the cerium oxide increased from 12.0 to 48 nm as the calcining temperature increased from 473 to 1273 K, in the pH range 8-9. The activation energy for the growth of cerium oxide nanoparticles was found to have very low values of 17.5 kJ/mol for pH = 8 and 16.0 kJ/mol for pH = 9.

  19. Effect of calcination temperature on the crystallite growth of cerium oxide nano-powders prepared by the co-precipitation process

    International Nuclear Information System (INIS)

    Cerium oxide nanocrystallites were synthesized by a co-precipitation process at a relatively low temperature, using cerium (III) nitrate as the starting material in a water solution with pH in the range of 8-9. The 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 at temperatures from 473 to 1273 K, face-centered cubic phase crystallization was observed by XRD. The crystallite size of the cerium oxide increased from 12.0 to 48 nm as the calcining temperature increased from 473 to 1273 K, in the pH range 8-9. The activation energy for the growth of cerium oxide nanoparticles was found to have very low values of 17.5 kJ/mol for pH = 8 and 16.0 kJ/mol for pH = 9.

  20. Moment dilution in the heavy fermion compound Ce2Bi

    International Nuclear Information System (INIS)

    The heavy fermion compound Ce2Bi has two inequivalent Ce-sites. La was doped on these sites to study the influence of the antiferromagnetic order on the high electronic contribution of the specific heat (γHT(T>TN)∼340mJ/Ce-molK2). The slightly larger La atom replaces the Ce2 site first and then subsequently the Ce1 site in the La2Sb structure. Lattice parameters, magnetic susceptibility and specific heat are used to elucidate the magnetic nature of the two different cerium sites. We find a somewhat enhanced γHT, a decrease in TN and furthermore a metamagnetic transition at 2.2T (2K), which is closely related to the long-range antiferromagnetic order. ((orig.))

  1. Panthenol-stabilized cerium dioxide nanoparticles for cosmeceutic formulations against ROS-induced and UV-induced damage.

    Science.gov (United States)

    Zholobak, N M; Shcherbakov, A B; Bogorad-Kobelska, A S; Ivanova, O S; Baranchikov, A Ye; Spivak, N Ya; Ivanov, V K

    2014-01-01

    A method of panthenol-stabilized cerium dioxide nanoparticles synthesis was developed and their effect on the survival rate of human epidermoid cancer cells HEp-2 and diploid epithelial swine testicular cell line (ST-cells) under oxidative stress conditions induced by hydrogen peroxide introduction and UV irradiation was studied. The results obtained indicate that the use of panthenol as a stabilizer supposedly provides a substantial increase in the efficiency of protection. The degree of protection is determined by panthenol-to-ceria molar ratio. The combination of panthenol and nano-ceria protects biological objects under study from reactive oxygen species (ROS) and UV-irradiation more effectively than individual panthenol or ceria. The protective action of panthenol-stabilized cerium dioxide nanoparticles depends strongly on their composition and the means of their application. PMID:24300997

  2. Real-time observation of dynamic process of oxygen vacancy migration in cerium oxides under electric field

    International Nuclear Information System (INIS)

    The dynamic process of oxygen vacancy migration driven by the external electric field is directly observed at atomic scale in the cerium oxides (CeO2) thin film by in-situ transmission electron microscopy method. When a bias voltage of a proper value is applied across the CeO2 film, the oxygen vacancies are formed near the interface of CeO2/anode, followed by their migration along the direction of the external electric field. The structural modulation occurs in the [110] zone axis due to the ordering of oxygen vacancies. The migration of oxygen vacancies results in the reversible structural transformation, i.e., releasing and storing oxygen processes in CeO2, which is of great significance for the ionic and electronic applications of the cerium oxides materials, such as oxygen pump, gas sensor, resistive random access memory, etc

  3. Real-time observation of dynamic process of oxygen vacancy migration in cerium oxides under electric field

    Energy Technology Data Exchange (ETDEWEB)

    Li, Xiaomin; Qi, Kuo; Sun, Muhua; Huang, Qianming; Xu, Zhi, E-mail: xuzhi@iphy.ac.cn, E-mail: xdbai@iphy.ac.cn; Wang, Wenlong [Beijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of Sciences, Beijing 100190 (China); Bai, Xuedong, E-mail: xuzhi@iphy.ac.cn, E-mail: xdbai@iphy.ac.cn [Beijing National Laboratory for Condensed Matter Physics and Institute of Physics, Chinese Academy of Sciences, Beijing 100190 (China); Collaborative Innovation Center of Quantum Matter, Beijing 100871 (China)

    2015-11-23

    The dynamic process of oxygen vacancy migration driven by the external electric field is directly observed at atomic scale in the cerium oxides (CeO{sub 2}) thin film by in-situ transmission electron microscopy method. When a bias voltage of a proper value is applied across the CeO{sub 2} film, the oxygen vacancies are formed near the interface of CeO{sub 2}/anode, followed by their migration along the direction of the external electric field. The structural modulation occurs in the [110] zone axis due to the ordering of oxygen vacancies. The migration of oxygen vacancies results in the reversible structural transformation, i.e., releasing and storing oxygen processes in CeO{sub 2}, which is of great significance for the ionic and electronic applications of the cerium oxides materials, such as oxygen pump, gas sensor, resistive random access memory, etc.

  4. Development of electrolytic process in molten salt media for light rare-earth metals production. The metallic cerium electrodeposition

    International Nuclear Information System (INIS)

    The development of molten salt process and the respective equipment aiming rare-earth metals recovery was described. In the present case, the liquid cerium metal electrodeposition in a molten electrolytes of cerium chloride and an equimolar mixture of sodium and potassium chlorides in temperatures near 800C was studied. Due the high chemical reactivity of the rare-earth metals in the liquid state and their molten halides, an electrolytic cell was constructed with controlled atmosphere, graphite crucibles and anodes and a tungsten cathode. The electrolytic process variables and characteristics were evaluated upon the current efficiency and metallic product purity. Based on this evaluations, were suggested some alterations on the electrolytic reactor design and upon the process parameters. (author). 90 refs, 37 figs, 20 tabs

  5. Real-time observation of dynamic process of oxygen vacancy migration in cerium oxides under electric field

    Science.gov (United States)

    Li, Xiaomin; Qi, Kuo; Sun, Muhua; Huang, Qianming; Xu, Zhi; Wang, Wenlong; Bai, Xuedong

    2015-11-01

    The dynamic process of oxygen vacancy migration driven by the external electric field is directly observed at atomic scale in the cerium oxides (CeO2) thin film by in-situ transmission electron microscopy method. When a bias voltage of a proper value is applied across the CeO2 film, the oxygen vacancies are formed near the interface of CeO2/anode, followed by their migration along the direction of the external electric field. The structural modulation occurs in the [110] zone axis due to the ordering of oxygen vacancies. The migration of oxygen vacancies results in the reversible structural transformation, i.e., releasing and storing oxygen processes in CeO2, which is of great significance for the ionic and electronic applications of the cerium oxides materials, such as oxygen pump, gas sensor, resistive random access memory, etc.

  6. Preparation and properties of a cerium-containing hydroxyapatite coating on commercially pure titanium by micro-arc oxidation

    Institute of Scientific and Technical Information of China (English)

    HUANG Yong; WANG Yingjun; NING Chengyun; NAN Kaihui; HAN Yong

    2008-01-01

    A porous cerium-containing hydroxyapatite coating on commercially pure titanium was prepared by micro-arc oxidation (MAO) in an electrolytic solution containing calcium acetate, β-glycerol phosphate disodium salt pentahydrate (β-GP), and cerium nitrate. The thickness, phase, composition morphology, and biocompatibility of the oxide coating were characterized by X-ray diffraction (XRD), electron probe microanalysis (EPMA), scanning electron microscopy (SEM) with energy dispersive X-ray spectrometer (EDS), and cell culture. The thickness of the MAO film is about 15-25μm, and the coating is porous and uneven, without any apparent interface to the titanium substrates. The results of XRD and EDS show that the porous coating is made up of hydroxyapatite (HA) film containing Ce. The favorable osteoblast cell affinity makes the Ce-HA film have a good biocompatibility. The Ce-HA film is expected to have significant medical applications as dental implants and artificial bone joints.

  7. Structure phase transformation and equation of state of cerium metal under pressures up to 51 GPa

    Science.gov (United States)

    Ce, Ma; Zuo-Yong, Dou; Hong-Yang, Zhu; Guang-Yan, Fu; Xiao, Tan; Bin, Bai; Peng-Cheng, Zhang; Qi-Liang, Cui

    2016-04-01

    This study presents high pressure phase transitions and equation of states of cerium under pressures up to 51 GPa at room temperature. The angle-dispersive x-ray diffraction experiments are carried out using a high energy synchrotron x-ray source. The bulk moduli of high pressure phases of cerium are calculated using the Birch–Murnaghan equation. We discuss and correct several previous controversial conclusions, which are caused by the measurement accuracy or personal explanation. The c/a axial ratio of ε-Ce has a maximum value at about 29 GPa, i.e., c/a ≈ 1.690. Project supported by the National Natural Science Foundation of China (Grant No. NSAF.U1330115) and the National Major Scientific Instrument and Equipment Development Project of China (Grant No. 2012YQ130234).

  8. Electron microscopy investigations of the organization of cerium oxide nanocrystallites and polymers developed in polyvinylpyrrolidone-assisted polyol synthesis process

    Energy Technology Data Exchange (ETDEWEB)

    Horiuchi, Shin, E-mail: s.horiuchi@aist.go.jp; Hanada, Takeshi [Nanosystem Research Institute, National Institute of Advanced Industrial Science and Technology (AIST) (Japan); Izu, Noriya; Matsubara, Ichiro [Advanced Manufacturing Research Institute, National Institute of Advanced Industrial Science and Technology (AIST) (Japan)

    2012-03-15

    The microstructures and the organization mechanism of cerium oxide (ceria) nanospheres were investigated by transmission electron microscopy. The ceria nanospheres with the diameter of 50-150 nm were produced by the polyol synthesis method with cerium nitrate precursor and with polyvinylpyrrolidone (PVP) used as a protecting agent. Dose-limited observations performed by energy-filtering transmission electron microscopy revealed that the ceria nanospheres were the aggregated products consisting of ceria nanocrystallites {approx}3 nm in size and PVP-derived polymer products. It was found that the ceria nanocrystallites were oriented within the nanospheres by high-resolution transmission electron microscopy and selected-area electron diffraction. Selective adsorption of PVP on the crystal facets of the ceria nanocrystallites was suggested, and the aggregation of the PVP-adsorbed ceria through cross-linking reaction of PVP causes the crystal orientation.

  9. Bioaccumulation of cerium and neodymium by Bacillus cereus isolated from rare earth environments of Chavara and Manavalakurichi, India

    International Nuclear Information System (INIS)

    Rare earth elements (REEs) are among the common minerals in the Rare earth environment that are very precious and also enhance soil properties. The aim of this present study is to evaluate the accumulation of REEs by bacterial isolates of rare earth environment. Morphological and biochemical characterization were done for 37 bacterial isolates and also molecular studies were carried out using 16S rRNA sequencing method. The assessment of REEs composition in soil samples of Chavara and Manavalakurichi analyzed using Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) showed the abundance of Cerium and Neodymium among lanthanides. The bioaccumulation study of rare earth elements by Bacillus cereus were accomplished employing FT-IR spectrum and ICP-OES analysis. The significant accumulation of rare earth elements especially Cerium and Neodymium was noticed in Bacillus cereus isolated from rare earth environment. (author)

  10. Structural and morphological evolution of cerium oxide thin film on silicon prepared by metal-organic decomposition route

    International Nuclear Information System (INIS)

    Thin film of cerium oxide (CeO2) were prepared on silicon (Si) substrate by metal organic decomposition route. 0.25 M of cerium (III) acetylacetonate (acac) was used as starting materials with the addition of methanol and acetic acid as solvents. Oxide conversion of the film by thermal treatment was conducted at temperature ranging from 400 degree Celsius to 1000 degree Celsius for 15 min in argon ambient. X-ray diffraction (XRD) analysis utilizing Cukα radiation (Model Brukker DiffracPlus), Filmetrics system measurement, field emission scanning electron microscope (FESEM) (Model Zeiss Supra 35 VP FESEM) and atomic force microscopy (AFM) (Model SII Nanonavi) were employed to characterize the phase formed and morphologies of the film produced. (author)

  11. Density-functional theory for f-electron systems. The α-γ phase transition in cerium

    International Nuclear Information System (INIS)

    Rare earths are technologically important and scientifically highly interesting elements. The description of the volume collapse exhibited by some rare earth metals poses a great challenge to density-functional theory (DFT) since local/semi-local functionals (LDA/GGA) only partially capture the associated phase transitions. In this work this problem is approached by treating all electrons at the same quantum mechanical level, using both hybrid functionals (e.g. PBE0 and HSE06) and exact-exchange plus correlation in the random-phase approximation (EX+cRPA). The performance of recently developed beyond RPA schemes is also assessed. The isostructural α-γ phase transition in cerium is the most studied. The exact exchange contribution in PBE0 and HSE06 is crucial to produce two distinct solutions that can be associated with the α and γ phases. The two solutions emerge in bulk as well as in cluster calculations. Most notable is their presence in the cerium dimer. However, quantitative agreement with the extrapolated phase diagram requires EX+cRPA. So far the EX+cRPA correction can only be applied to cerium clusters and not to the bulk. A cluster of 19 atoms cut from the fcc crystal structure (the same that characterizes the α and γ phases) was therefore determined as representative. (EX+cRPA) rate at PBE0 for Ce19 provides good agreement with the extrapolated transition pressure to zero temperature. We predict that a pressure induced phase transition should exist at or close to zero. A finite temperature phase diagram can be drawn in reasonable agreement with experiment by adding entropic effects. The cerium neighbors are also studied: lanthanum, which has no f electrons, praseodymium, with three f electrons and a volume collapse, and neodymium, with four f electrons and no volume collapse. Multiple solutions are also present for these f electron elements, confirming the importance of exact-exchange for f electron systems.

  12. Mixtures of room temperature ionic liquid/ethanol solutions as electrolytic media for cerium oxide thin layer electrodeposition

    Energy Technology Data Exchange (ETDEWEB)

    Lair, V., E-mail: virginie-lair@chimie-paristech.f [Laboratoire d' Electrochimie, Chimie des Interfaces et Modelisation pour l' Energie, LECIME, CNRS UMR 7575-Chimie Paristech (ENSCP)-Paris, 11, rue Pierre et Marie Curie, 75231 Paris Cedex 05 (France); Sirieix-Plenet, J.; Gaillon, L.; Rizzi, C. [UPMC University Paris 06, UMR 7195, Laboratoire de Physicochimie des Electrolytes, Colloides et Sciences Analytiques (PECSA), F-75005 Paris (France); CNRS, UMR 7195, PECSA, F-75005 Paris (France); ESPCI, UMR 7195, PECSA, F-75005 Paris (France); Ringuede, A. [Laboratoire d' Electrochimie, Chimie des Interfaces et Modelisation pour l' Energie, LECIME, CNRS UMR 7575-Chimie Paristech (ENSCP)-Paris, 11, rue Pierre et Marie Curie, 75231 Paris Cedex 05 (France)

    2010-12-30

    A cerium oxide thin layer was electrodeposited onto stainless steel, using mixed room temperature ionic liquid (the 1-methyl-3-butylimidazolium bis(trifluoromethyl sulfonyl)imide)/ethanol solutions, as electrolytic medium. The hydrophobic ionic liquid content is one of the main parameters in the morphology control influencing the ceria growth rate and crystallinity. Micro-nano structural properties and electrical behaviour are presented, using XRD, SEM/EDS and impedance spectroscopy, as a function of electrodeposition conditions.

  13. Mixtures of room temperature ionic liquid/ethanol solutions as electrolytic media for cerium oxide thin layer electrodeposition

    International Nuclear Information System (INIS)

    A cerium oxide thin layer was electrodeposited onto stainless steel, using mixed room temperature ionic liquid (the 1-methyl-3-butylimidazolium bis(trifluoromethyl sulfonyl)imide)/ethanol solutions, as electrolytic medium. The hydrophobic ionic liquid content is one of the main parameters in the morphology control influencing the ceria growth rate and crystallinity. Micro-nano structural properties and electrical behaviour are presented, using XRD, SEM/EDS and impedance spectroscopy, as a function of electrodeposition conditions.

  14. Study on corrosion resistance of the BTESPT silane cooperating with rare earth cerium on the surface of aluminum-tube

    Institute of Scientific and Technical Information of China (English)

    肖围; 满瑞林; 缪畅; 彭天兰

    2010-01-01

    Bis-3-(triethoxysilyl)propyltetrasulfide(BTESPT) silane-rare earth cerium composite coatings on aluminum-tube were prepared at 60 °C by immersion method.The performance of composite coatings to protect the aluminum-tube against corrosion was investigated with potentiodynamic polarization curves,electrochemical impedance spectroscopy(EIS),and salt spray test(SST).The results of potentiodynamic polarization curves and EIS indicated that the self-corrosion current decreased by two orders of magnitude and the i...

  15. The biological effects of subacute inhalation of diesel exhaust following addition of cerium oxide nanoparticles in atherosclerosis-prone mice

    Energy Technology Data Exchange (ETDEWEB)

    Cassee, Flemming R., E-mail: flemming.cassee@rivm.nl [National Institute for Public Health and the Environment, PO box 1, 3720 BA Bilthoven (Netherlands); Campbell, Arezoo, E-mail: acampbell@westernu.edu [Western University of Health Sciences, Pomona, CA (United States); Boere, A. John F., E-mail: john.boere@rivm.nl [National Institute for Public Health and the Environment, PO box 1, 3720 BA Bilthoven (Netherlands); McLean, Steven G., E-mail: smclean1@staffmail.ed.ac.uk [BHF/University Centre for Cardiovascular Sciences, University of Edinburgh, Edinburgh (United Kingdom); Duffin, Rodger, E-mail: Rodger.Duffin@ed.ac.uk [MRC Centre for Inflammation Research, University of Edinburgh, Edinburgh (United Kingdom); Krystek, Petra, E-mail: petra.krystek@philips.com [Philips Innovation Services, Eindhoven (Netherlands); Gosens, Ilse, E-mail: Ilse.gosens@rivm.nl [National Institute for Public Health and the Environment, PO box 1, 3720 BA Bilthoven (Netherlands); Miller, Mark R., E-mail: Mark.Miller@ed.ac.uk [BHF/University Centre for Cardiovascular Sciences, University of Edinburgh, Edinburgh (United Kingdom)

    2012-05-15

    Background: Cerium oxide (CeO{sub 2}) nanoparticles improve the burning efficiency of fuel, however, little is known about health impacts of altered emissions from the vehicles. Methods: Atherosclerosis-prone apolipoprotein E knockout (ApoE{sup -/-}) mice were exposed by inhalation to diluted exhaust (1.7 mg/m{sup 3}, 20, 60 or 180 min, 5 day/week, for 4 weeks), from an engine using standard diesel fuel (DE) or the same diesel fuel containing 9 ppm cerium oxide nanoparticles (DCeE). Changes in hematological indices, clinical chemistry, atherosclerotic burden, tissue levels of inflammatory cytokines and pathology of the major organs were assessed. Results: Addition of CeO{sub 2} to fuel resulted in a reduction of the number (30%) and surface area (10%) of the particles in the exhaust, whereas the gaseous co-pollutants were increased (6-8%). There was, however, a trend towards an increased size and complexity of the atherosclerotic plaques following DE exposure, which was not evident in the DCeE group. There were no clear signs of altered hematological or pathological changes induced by either treatment. However, levels of proinflammatory cytokines were modulated in a brain region and liver following DCeE exposure. Conclusions: These results imply that addition of CeO{sub 2} nanoparticles to fuel decreases the number of particles in exhaust and may reduce atherosclerotic burden associated with exposure to standard diesel fuel. From the extensive assessment of biological parameters performed, the only concerning effect of cerium addition was a slightly raised level of cytokines in a region of the central nervous system. Overall, the use of cerium as a fuel additive may be a potentially useful way to limit the health effects of vehicle exhaust. However, further testing is required to ensure that such an approach is not associated with a chronic inflammatory response which may eventually cause long-term health effects.

  16. Study on recovering directly the commercial cerium oxide and total of residue rare earths from Dongpao bastnasite concentrate

    International Nuclear Information System (INIS)

    A technology for decomposition roasting and sequential leaching processes of Dong Pao bastnasite concentrate to recover directly commercial cerium oxide and total of residue rare earth elements from the leaching solution of the roasted product have been investigated. The bastnasite concentrate is initially roasted at temperature range of 600 - 650 degC and for time of 4 hrs in order to decompose and convert the hardly soluble carbonate forms of ore into easily soluble oxide. The roasted solid is then leached with sulfuric acid solution of 6N at 60 degC for 4 hrs to convert rare earths in oxide and fluoride form into rare earth sulfate. The recovery yield of rare earths of these stages is more than 95%. The attention has especially been paid on recovering directly the commercial cerium oxide and total of residue rare earth element from the above leaching solution. Complex ions of CeSO42+, Ce(SO4)2, Ce(SO4)32- and Ce(SO4)44- exist in aqueous solution of cerium (IV) sulfate. Based on the property, the method of ion - sieve with DOWEX cation resin column has been applied to estimating separation of the ceric complex anions from Ln(III). The survey showed that most of the ceric complex anions are separated from total of residue rare earths. The latter which are absorbed in the cation column are recovered by elution of HCl of 4N. The recovery yield of cerium can only be reached 20% but the purity of that is very high, can be reached 99.6%. About 5 kg of CeO2 of high grade and 5 kg of TREO of commercial specification have been produced. (author)

  17. The biological effects of subacute inhalation of diesel exhaust following addition of cerium oxide nanoparticles in atherosclerosis-prone mice

    International Nuclear Information System (INIS)

    Background: Cerium oxide (CeO2) nanoparticles improve the burning efficiency of fuel, however, little is known about health impacts of altered emissions from the vehicles. Methods: Atherosclerosis-prone apolipoprotein E knockout (ApoE−/−) mice were exposed by inhalation to diluted exhaust (1.7 mg/m3, 20, 60 or 180 min, 5 day/week, for 4 weeks), from an engine using standard diesel fuel (DE) or the same diesel fuel containing 9 ppm cerium oxide nanoparticles (DCeE). Changes in hematological indices, clinical chemistry, atherosclerotic burden, tissue levels of inflammatory cytokines and pathology of the major organs were assessed. Results: Addition of CeO2 to fuel resulted in a reduction of the number (30%) and surface area (10%) of the particles in the exhaust, whereas the gaseous co-pollutants were increased (6–8%). There was, however, a trend towards an increased size and complexity of the atherosclerotic plaques following DE exposure, which was not evident in the DCeE group. There were no clear signs of altered hematological or pathological changes induced by either treatment. However, levels of proinflammatory cytokines were modulated in a brain region and liver following DCeE exposure. Conclusions: These results imply that addition of CeO2 nanoparticles to fuel decreases the number of particles in exhaust and may reduce atherosclerotic burden associated with exposure to standard diesel fuel. From the extensive assessment of biological parameters performed, the only concerning effect of cerium addition was a slightly raised level of cytokines in a region of the central nervous system. Overall, the use of cerium as a fuel additive may be a potentially useful way to limit the health effects of vehicle exhaust. However, further testing is required to ensure that such an approach is not associated with a chronic inflammatory response which may eventually cause long-term health effects.

  18. Study on cerium-doped nano-TiO2 coatings for corrosion protection of 316 L stainless steel

    Science.gov (United States)

    Li, Suning; Wang, Qian; Chen, Tao; Zhou, Zhihua; Wang, Ying; Fu, Jiajun

    2012-04-01

    Many methods have been reported on improving the photogenerated cathodic protection of nano-TiO2 coatings for metals. In this work, nano-TiO2 coatings doped with cerium nitrate have been developed by sol-gel method for corrosion protection of 316 L stainless steel. Surface morphology, structure, and properties of the prepared coatings were investigated by X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy and energy dispersive X-ray spectroscopy. The corrosion protection performance of the prepared coatings was evaluated in 3 wt% NaCl solution by using electrochemical techniques in the presence and absence of simulated sunlight illumination. The results indicated that the 1.2% Ce-TiO2 coating with three layers exhibited an excellent photogenerated cathodic protection under illumination attributed to the higher separation efficiency of electron-hole pairs and higher photoelectric conversion efficiency. The results also showed that after doping with an appropriate concentration of cerium nitrate, the anti-corrosion performance of the TiO2 coating was improved even without irradiation due to the self-healing property of cerium ions.

  19. The solubility of cerium in La{sub 2}Ti{sub 2}O{sub 7} by DFT + U calculations

    Energy Technology Data Exchange (ETDEWEB)

    Liu, C.G.; Yang, D.Y. [School of Nuclear Science and Technology, Lanzhou University, Lanzhou, 730000 (China); Chen, L.J. [School of Nuclear Science and Technology, Lanzhou University, Lanzhou, 730000 (China); Henan Electric Power Generation Limited Company Pingdingshan Generation Branch, China Power Investment Corporation, Pingdingshan, 467312 (China); Liu, H.; Xia, Y.; Wen, J.; Dong, L.Y.; Zhang, K.Q.; Xiang, A.Z. [School of Nuclear Science and Technology, Lanzhou University, Lanzhou, 730000 (China); Li, Y.H., E-mail: liyuhong@lzu.edu.cn [School of Nuclear Science and Technology, Lanzhou University, Lanzhou, 730000 (China)

    2015-11-05

    To investigate the solubility of cerium in La{sub 2}Ti{sub 2}O{sub 7}, the density functional theory plus Hubbard U correction (DFT + U) approach is employed. The geometrical structure, solution energy and electronic structure of La{sub 2−y}Ce{sub y}Ti{sub 2}O{sub 7} (0 ≤ y ≤ 2) have been analyzed. The results reveal that the La{sub 2}Ti{sub 2}O{sub 7}–Ce{sub 2}Ti{sub 2}O{sub 7} solid solution exits over the entire range of cerium content. The calculated increase in the O{sub 48f} 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 La{sub 2}Ti{sub 2}O{sub 7}–Ce{sub 2}Ti{sub 2}O{sub 7} solid solution suggest that cerium exhibits a reduced charge state in the solid solution. - Highlights: • La{sub 2}Ti{sub 2}O{sub 7}–Ce{sub 2}Ti{sub 2}O{sub 7} solid solution exits over the entire range of cerium content from 0 to 2. • Cerium incorporation in La{sub 2}Ti{sub 2}O{sub 7} may lead to increased radiation resistance of La{sub 2−y}Ce{sub y}Ti{sub 2}O{sub 7} (0 ≤ y ≤ 2) . • Cerium in the solid solution of La{sub 2−y}Ce{sub y}Ti{sub 2}O{sub 7} (0 ≤ y ≤ 2) exhibits a reduced charge state.

  20. Cytotoxicity and antibacterial activity of gold-supported cerium oxide nanoparticles

    Directory of Open Access Journals (Sweden)

    Suresh Babu K

    2014-11-01

    Full Text Available K Suresh Babu,1,† M Anandkumar,1,† TY Tsai,2 TH Kao,2 B Stephen Inbaraj,2 BH Chen2,31Centre for Nano Sciences and Technology, Madanjeet School of Green Energy Technologies, Pondicherry University, Kalapet, India; 2Department of Food Science, 3Graduate Institute of Medicine, Fu Jen University, Taipei, Taiwan†These authors contributed equally to this workBackground: Cerium oxide nanoparticles (CeO2 have been shown to be a novel therapeutic in many biomedical applications. Gold (Au nanoparticles have also attracted widespread interest due to their chemical stability and unique optical properties. Thus, decorating Au on CeO2 nanoparticles would have potential for exploitation in the biomedical field. Methods: In the present work, CeO2 nanoparticles synthesized by a chemical combustion method were supported with 3.5% Au (Au/CeO2 by a deposition-precipitation method. The as-synthesized Au, CeO2, and Au/CeO2 nanoparticles were evaluated for antibacterial activity and cytotoxicity in RAW 264.7 normal cells and A549 lung cancer cells. Results: The as-synthesized nanoparticles were characterized by X-ray diffraction, scanning and transmission electron microscopy, and ultraviolet-visible measurements. The X-ray diffraction study confirmed the formation of cubic fluorite-structured CeO2 nanoparticles with a size of 10 nm. All synthesized nanoparticles were nontoxic towards RAW 264.7 cells at doses of 0–1,000 µM except for Au at >100 µM. For A549 cancer cells, Au/CeO2 had the highest inhibitory effect, followed by both Au and CeO2 which showed a similar effect at 500 and 1,000 µM. Initial binding of nanoparticles occurred through localized positively charged sites in A549 cells as shown by a shift in zeta potential from positive to negative after 24 hours of incubation. A dose-dependent elevation in reactive oxygen species indicated that the pro-oxidant activity of the nanoparticles was responsible for their cytotoxicity towards A549 cells. In