Corrosion of niobium-1 percent zirconium alloy and yttria by lithium at high flow velocities

Lithium corrosion of niobium zirconium alloys and yttrium oxides at high flow velocitie

Synthesis of Al[2]O[3]-ZrO[2] powders from differently concentrated suspensions with a spray drying technique

The composite powders of aluminium and zirconium oxides containing 10, 50 and 90 mol % Al{3+} without a stabilizer have been obtained from suspensions using a spray drying method. The powders obtained at equal mole ratios of zirconium and aluminum in the original solution (0.5:0.5 mol/l) have the largest contents of cubic and tetragonal phases of ZrO[2], strictly uniform distribution of phases and the largest value of the specific surface area. The particles with two different morphologies have been obtained: crystalline particles of oxides uniformly distributed in a particle and particles in membrane consisting of zirconium oxide or mixed oxides. It has been experimentally shown that zirconium oxide stabilizes the amorphous phase of aluminum oxide, and aluminum oxide increases the temperature of crystallization of zirconium oxide

Magnesium-zinc reduction is effective in preparation of metals

Uranium, thorium, and plutonium are effectively prepared by magnesium-zinc reduction, using uranium oxides, thorium dioxide, and plutonium dioxide as starting materials. This technique is also useful in performing reduction of metals such as zirconium and titanium

Effect of anodization on the surface characteristics and electrochemical behaviour of zirconium in artificial saliva

The paper is focused on elaboration of ZrO2 films on pure zirconium via anodizing inphosphoric acid with and without fluoride at constant potentials of 30 V and 60 V. Thestructure and composition of the films were investigated using scanning electronicmicroscopy, Raman spectroscopy and X-ray photoelectron spectroscopy. The composition ofthe oxides formed at both potentials can be identified as monoclinic ZrO2. In addition to Zrand O, the layers formed in phosphoric acid contain phosphorus originating from thephosphoric acid. When the phosphoric acid solution contains NaF, fluorine is alsoincorporated into the oxide layer. The oxides formed at a higher voltage have greaterroughness than those formed at 30 V. Anodized samples exhibit smaller current densitiesduring anodic polarization compared to the as-received zirconium covered with native oxide.Fil: Romonti, Daniela E.. Faculty of Applied Chemistry and Materials Science; RumaniaFil: Gomez Sanchez, Andrea Valeria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Milošev, Ingrid. Jožef Stefan Institute; EsloveniaFil: Demetrescu, Ioana. Faculty of Applied Chemistry and Materials Science; RumaniaFil: Ceré, Silvia. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentin

The determination of major and some minor constituents in lead zirconate-titanate compositions by x-ray fluorescence and atomic absorption spectrometry

An accurate X-ray fluorescence spectrometric method is described for the determination of lead, zirconium and titanium in lead zirconate-titanate ceramics. Careful matching of samples and standards by a borax fusion method resulted in a relative standard deviation of about 0.2% for the major constituents. The determination, after separation, of the unreacted oxide of lead by atomic absorption spectrometry, and of the unreacted oxides of zirconium and titanium by X-ray fluorescence spectrometry is also described. An X-ray fluorescence spectrometric method is proposed for the determination of dope elements (K, La, Sm, Yb) with internal standards (Ca, Ce, Cr, Ni respectively). The magnesium dope is determined by atomic-absorption spectrometry with standard addition

Method of forming dynamic membrane on stainless steel support

A suitable member formed from sintered, powdered, stainless steel is contacted with a nitrate solution of a soluble alkali metal nitrate and a metal such as zirconium in a pH range and for a time sufficient to effect the formation of a membrane of zirconium oxide preferably including an organic polymeric material such as polyacrylic acid

Facile synthesis and enhanced visible light photocatalytic activity of N and Zr co-doped TiO2 nanostructures from nanotubular titanic acid precursors

Zr/N co-doped TiO2 nanostructures were successfully synthesized using nanotubular titanic acid (NTA) as precursors by a facile wet chemical route and subsequent calcination. These Zr/N-doped TiO2 nanostructures made by NTA precursors show significantly enhanced visible light absorption and much higher photocatalytic performance than the Zr/N-doped P25 TiO2 nanoparticles. Impacts of Zr/N co-doping on the morphologies, optical properties, and photocatalytic activities of the NTA precursor-based TiO2 were thoroughly investigated. The origin of the enhanced visible light photocatalytic activity is discussed in detail.Comment: 8 pages, 7 figure

Anion exchange on hydrous zirconium oxide materials: application for selective iodate removal

The radioactive 129I is a top-priority radionuclide due to its the long half-life (1.57 × 107 years) and high mobility. Because of the planned and accidental releases to the environment, specific separation technologies are required to limit the potential radiation dose to human beings. Zirconium oxides are known for their adsorption capability and selectivity to oxyanions and here the applicability to selective IO3− removal has been investigated regarding the uptake mechanism, regeneration and competition caused by other anions, like environmentally relevant SO42−. Granular aggregates of hydrous zirconium oxides with and without Sb doping showed high potential for the selective IO3− removal in the presence of competing anions, like the forementioned SO42− (apparent capacity between 0.1–0.4 meq g−1 depending on SO42− concentration). The main uptake mechanism was found to be outer-sphere complexation (ion-exchange) to the protonated hydroxyl groups of hydrous zirconium oxides, but also minor mechanisms were identified including inner-sphere complexation and reduction to I−. The materials were observed to be easily and successively regenerated using dilute acid. Hydrous zirconium oxides showed high potential for IO3− removal from waste solutions regarding technical (high selectivity and apparent capacity) and ecological/economic (feasible regeneration) aspects.The radioactive I-129 is a top-priority radionuclide due to its the long half-life (1.57 x 10(7) years) and high mobility. Because of the planned and accidental releases to the environment, specific separation technologies are required to limit the potential radiation dose to human beings. Zirconium oxides are known for their adsorption capability and selectivity to oxyanions and here the applicability to selective IO3- removal has been investigated regarding the uptake mechanism, regeneration and competition caused by other anions, like environmentally relevant SO42-. Granular aggregates of hydrous zirconium oxides with and without Sb doping showed high potential for the selective IO3- removal in the presence of competing anions, like the forementioned SO42- (apparent capacity between 0.1-0.4 meq g(-1) depending on SO42- concentration). The main uptake mechanism was found to be outer-sphere complexation (ion-exchange) to the protonated hydroxyl groups of hydrous zirconium oxides, but also minor mechanisms were identified including inner-sphere complexation and reduction to I-. The materials were observed to be easily and successively regenerated using dilute acid. Hydrous zirconium oxides showed high potential for IO3- removal from waste solutions regarding technical (high selectivity and apparent capacity) and ecological/economic (feasible regeneration) aspects.Peer reviewe

Stabilized tetragonal zirconium oxide as a support for catalysts: evolution of the texture and structure on calcination in static air

Single-phase tetragonal zirconium oxides have been made by the incorporation of 5.4 mol-% of Y3+ or La3+ in ZrO2 to form solid solutions. The samples were prepared by controlled coprecipitation from aqueous solutions of the respective metal chlorides at room temperature and at a constant pH of 10, followed by calcination at 500°C (in the case of the Y3+ -doped sample) or 600°C (in the case of the La3+ -doped sample) to effectuate the crystallization into the tetragonal phase. The process of crystallization of the hydrous zirconia precursor was found to be retarded by the incorporation of Y3+ or La3+, the latter giving the greater effect. Upon crystallization, stabilized tetragonal samples were obtained with high specific surface areas (SBET ca. 88 m2 g¿1 for both the samples) and well-developed mesoporous textures but without any microporosity. Both the Y3+ - and the La3+ -alloyed ZrO2 samples were found to fully retain the tetragonal phase upon calcination over the entire range of temperatures studied (up to 900°C). The thermal stability of the texture of zirconia was found to be considerably improved, in comparison with the undoped monoclinic material, by the stabilization of the crystal structure in the defect tetragonal form. In particular, incorporation of 5.4 mol-% of La3+ resulted in a support material which had a remarkable thermal stability. It is shown that the improvements in the thermal stability are derived from a strong inhibition of the processes of crystallite growth and the accompanying intercrystallite sintering and thus of the process of mass transport; the mass transport probably occurs by a mechanism of surface diffusion