Local structure in solid solutions of stabilised zirconia with actinide dioxides (UO2, NpO2)

被引:7
|
作者
Walter, Marcus [1 ]
Somers, Joseph [1 ]
Bouexiere, Daniel [1 ]
Rothe, Joerg [2 ]
机构
[1] European Commiss, Joint Res Ctr, Inst Transuranium Elements, D-76125 Karlsruhe, Germany
[2] Karlsruher Inst Technol, Inst Nukl Entsorgung, D-76021 Karlsruhe, Germany
关键词
Transmutation; Nuclear fuel; Zirconium; Uranium; Neptunium; EXAFS; X-RAY-ABSORPTION; EXAFS; TRANSMUTATION; FLUORITE; OXIDES; ZRO2;
D O I
10.1016/j.jssc.2011.02.014
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
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 degrees C in Ar/H-2 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 angstrom at 6 mol% actinide to 2.18 angstrom 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. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:911 / 914
页数:4
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