81,337 research outputs found

    Stabilization of Tungsten-Uranium Dioxide Composites Under Thermal Cycling Conditions

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    Uranium losses during thermal cycling of tungsten - uranium dioxide composites to 2500 C in flowing purified hydrogen for specimens initially containing 35 volume percent uranium dioxide were reduced by the use of thorium dioxide, calcium oxide, or yttrium oxide as additives in solid solution with the uranium dioxide. The effectiveness of the additives decreased in the order yttrium oxide, calcium oxide, and thorium dioxide. Stabilization of uranium dioxide by calcium oxide or yttrium oxide can be explained in part on the basis of the introduction of oxygen vacancies into the fluorite lattice and the associated lowered partial molar free energy of oxygen. The difference in the effectiveness of calcium oxide and yttrium oxide is discussed, and a possible explanation of the observed behavior is proposed. Of the concentrations of yttrium oxide tested (i.e., 2. 5, 5, and 10 mole percent), 10 mole percent of yttrium oxide was the most effective in pre venting loss of uranium from composities

    Superconductivity and Magnetism in REFeAsO1-xFx (RE=Rare Earth Elements)

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    Fluoride-doped iron-based oxypnictides containing rare-earth gadolinium (GdFeAsO0.8F0.2) and co-doping with yttrium (Gd0.8Y0.2FeAsO0.8F0.2) have been prepared via conventional solid state reaction at ambient pressure. The non-yttrium substituted oxypnictide show superconducting transition as high as 43.9 K from temperature dependent resistance measurements with the Meissner effect observed at a lower temperature of 40.8 K from temperature dependent magnetization measurements. By replacing a small amount of gadolinium with yttrium Tc was observed to be lowered by 10 K which might be caused by a change in the electronic or magnetic structures since the crystal structure was not altered.Comment: 4 pages, 4 figures, Journal of Physics: Conference Series (Proceedings in the LT25 Low Temperature Physics Conference) Submitte

    The sulphidation properties of pre-oxidized yttrium-ion-implanted Incoloy 800H

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    On sulphidation of pre-oxidized yttrium-implanted Incoloy 800H an improvement in sulphidation resistance is obtained. Pre-oxidized krypton-implanted alloy and aluminium-implanted alloy have sulphidation rates which are about the same as that of non-implanted pre-oxidized Incoloy 800H. Scanning electron microscopy observations show that one of the effects of yttrium implantation is to decrease the corrosion rate at the alloy grain boundaries

    Enhanced co-solubilities of Ca and Si in YAG (Y3Al5O12)

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    General garnet structure (Ia3-d) is a forgiving host and can accommodate cations of varying sizes and valence states. Studies on highly yttrium doped alumina ceramics with Ca and Si contamination indicated that YAG precipitates in the ceramic had a propensity to allow simultaneous incorporation of small amounts of Ca and Si impurities in their structure. In this study, using chemical synthesis techniques it was shown that YAG can accommodate up to approximately 8 cation % Ca+2 and Si+4 (i.e. Ca+2/Y+3 and Si+4/Y+3) if they are incorporated together. Equilibrium conditions are established by calcining samples at 900 C for 2 hours and cooling the samples to room temperature in the furnace. Disappearing-phase method and energy dispersive X-ray spectroscopy (EDS) were used to determine solubility and co-solubility limits. Beyond the solubility limit phase separation occurred and three crystalline yttrium aluminate phases (YAG, YAP (yttrium aluminate perovskite, YAlO3), YAM (yttrium aluminate monoclinic, Y4Al2O9)) were observed. It is believed that the excess Ca and Si above co-solubility limit precipitate out in the form of an x-ray amorphous anorthite-like glass in the system

    Off-line studies of the laser ionization of yttrium at the IGISOL facility

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    A laser ion source is under development at the IGISOL facility, Jyvaskyla, in order to address deficiencies in the ion guide technique. The key elements of interest are those of a refractory nature, whose isotopes and isomers are widely studied using both laser spectroscopic and high precision mass measurement techniques. Yttrium has been the first element of choice for the new laser ion source. In this work we present a new coupled dye-Ti:Sapphire laser scheme and give a detailed discussion of the results obtained from laser ionization of yttrium atoms produced in an ion guide via joule heating of a filament. The importance of not only gas purity, but indeed the baseline vacuum pressure in the environment outside the ion guide is discussed in light of the fast gas phase chemistry seen in the yttrium system. A single laser shot model is introduced and is compared to the experimental data in order to extract the level of impurities within the gas cell.Comment: 18 pages submitted to NIM

    Transparent yttrium hydride thin films prepared by reactive sputtering

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    Metal hydrides have earlier been suggested for utilization in solar cells. With this as a motivation we have prepared thin films of yttrium hydride by reactive magnetron sputter deposition. The resulting films are metallic for low partial pressure of hydrogen during the deposition, and black or yellow-transparent for higher partial pressure of hydrogen. Both metallic and semiconducting transparent YHx films have been prepared directly in-situ without the need of capping layers and post-deposition hydrogenation. Optically the films are similar to what is found for YHx films prepared by other techniques, but the crystal structure of the transparent films differ from the well-known YH3 phase, as they have an fcc lattice instead of hcp

    Oxidation resistance of ODS alloy PM2000 from 880°C to 1400°C

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    Oxidation resistance of ODS alloy PM2000 from 880°C to 1400°

    Characterization of Grain Boundaries in Superplastically Deformed Y-TZP Ceramics

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    The effects of compressive deformation on the grain boundary characteristics of fine-grained Y-TZP have been investigated using surface spectroscopy, impedance analysis, and transmission electron microscopy. After sintering at low temperature (1150°C), the grain boundaries are covered by an ultrathin (1nm) yttrium-rich amorphous film. After deformation at 1200°–1300°C under low stress, some grain boundaries are no longer covered by the amorphous film. Yttrium segregation seems to occur only at wetted grain boundaries. Evidence has been found that the extent of dewetting increases with increasing applied stress
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