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Local structure in solid solutions of stabilised zirconia with actinide dioxides (UO2, NpO2)
Authors:Marcus Walter,Joseph Somers,Jö  rg Rothe
Affiliation:a European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O. Box 2340, D-76125 Karlsruhe, Germany
b Karlsruher Institut für Technologie, Institut für Nukleare Entsorgung (INE), P.O. Box 3640, D-76021 Karlsruhe, Germany
Abstract:The local structure of (Zr,Lu,U)O2−x and (Zr,Y,Np)O2−x solid solutions has been investigated by extended X-ray absorption fine structure (EXAFS). Samples were prepared by mixing reactive (Zr,Lu)O2−x and (Zr,Y)O2−x precursor materials with the actinide oxide powders, respectively. Sintering at 1600 °C in Ar/H2 yields a fluorite structure with U(IV) and Np(IV). As typical for stabilised zirconia the metal-oxygen and metal-metal distances are characteristic for the different metal ions. The bond lengths increase with actinide concentration, whereas highest adaptation to the bulk stabilised zirconia structure was observed for UO and NpO bonds. The ZrO bond shows only a slight increase from 2.14 Å at 6 mol% actinide to 2.18 Å at infinite dilution in UO2 and NpO2. The short interatomic distance between Zr and the surrounding oxygen and metal atoms indicate a low relaxation of Zr with respect to the bulk structure, i.e. a strong Pauling behaviour.
Keywords:Transmutation   Nuclear fuel   Zirconium   Uranium   Neptunium   EXAFS
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