Incorporation of uranium in pyrochlore oxides and pressure-induced phase transitions

被引:33
|
作者
Zhang, F. X. [1 ]
Lang, M. [1 ]
Tracy, C. [1 ]
Ewing, R. C. [1 ]
Gregg, D. J. [2 ]
Lumpkin, G. R. [2 ]
机构
[1] Univ Michigan, Dept Earth & Environm Sci, Ann Arbor, MI 48109 USA
[2] ANSTO, Inst Mat Engn, Kirrawee Dc, NSW 2232, Australia
基金
美国国家科学基金会;
关键词
Pyrochlore; Uranium; High pressure; INDUCED AMORPHIZATION; RADIATION TOLERANCE; CRYSTAL-CHEMISTRY; NUCLEAR-WASTE; FLUORITE-TYPE; IMMOBILIZATION; DISORDER; A(2)B(2)O(7); PLUTONIUM; LA2ZR2O7;
D O I
10.1016/j.jssc.2014.07.011
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Uranium-doped gadolinium zirconates with pyrochlore structure were studied at ambient and high-pressure conditions up to 40 GPa. The bonding environment of uranium in the structure was determined by x-ray photoelectron and Raman spectroscopies and x-ray diffraction. The uranium valence for samples prepared in air is mainly U6+, but U4+ is present in pyrochlores fabricated in an argon atmosphere. Rietveld refinement of the XRD pattern suggests that uranium ions in pyrochlores are on the 16d site in 6-fold coordination with oxygen. At pressures greater than 22 GPa, the pyrochlore structure transformed to a cotunnite-type phase. The cotunnite high-pressure phase transformed to a defect fluorite structure on the release of pressure. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:49 / 54
页数:6
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