Local structure in solid solutions of stabilised zirconia with actinide dioxides (UO2, NpO2) |
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Authors: | Marcus Walter,Joseph Somers,Jö rg Rothe |
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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 |
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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 UO and NpO bonds. The ZrO 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. |
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Keywords: | Transmutation Nuclear fuel Zirconium Uranium Neptunium EXAFS |
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