Charge distribution and local structure and speciation in the UO2+x and PuO2+x binary oxides for x ≤ 0.25

被引:69
作者
Conradson, SD
Begg, BD
Clark, DL
den Auwer, C
Ding, M
Dorhout, PK
Espinosa-Faller, FJ
Gordon, PL
Haire, RG
Hess, NJ
Hess, RF
Keogh, DW
Lander, GH
Manara, D
Morales, LA
Neu, MP
Paviet-Hartmann, P
Rebizant, J
Rondinella, VV
Runde, W
Tait, CD
Veirs, DK
Villella, PM
Wastin, F
机构
[1] Los Alamos Natl Lab, Div Chem, Los Alamos, NM 87545 USA
[2] Los Alamos Natl Lab, Mat Sci & Technol Div, Los Alamos, NM 87545 USA
[3] Los Alamos Natl Lab, Nucl Mat Technol Div, Los Alamos, NM 87545 USA
[4] Australian Nucl Sci & Technol Org, Menai, NSW 2234, Australia
[5] CEA, F-30207 Bagnols Sur Ceze, France
[6] Colorado State Univ, Ft Collins, CO 80523 USA
[7] Ctr Marista Estudios Super, Merida, Yucatan, Mexico
[8] Oak Ridge Natl Lab, Oak Ridge, TN 37831 USA
[9] Pacific NW Natl Lab, Richland, WA 99352 USA
[10] Commiss European Communities, Joint Res Ctr, Inst Transuranium Elements, D-76125 Karlsruhe, Germany
关键词
speciation; local structure; X-ray absorption fine structure spectroscopy; urania; plutonia; mixed valence actinide oxide; XAFS;
D O I
10.1016/j.jssc.2004.09.029
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The local structure and chemical speciation of the mixed valence, fluorite-based oxides UO2+x (0.00 <= x <= 0.20) and PuO2+x/PuO2+x-y(OH)(2y)center dot zH(2)O have been determined by U/Pu L-m XAFS spectroscopy. The U spectra indicate (1) that the O atoms are incorporated as oxo groups at short (1.75 angstrom) U-O distances consistent with U(VI) concomitant with a large range of U displacements that reduce the apparent number of U neighbors and (2) that the UO2 fraction remains intact implying that these O defects interact to form Clusters and give the heterogeneous structure consistent with the diffraction patterns. The PuO2+x system, which does not show a separate phase at its x = 0.25 endpoint, also displays (1) oxo groups at longer 1.9 angstrom distances consistent with Pu(V + delta), (2) a multisite Pu-O distribution even when x is close to zero indicative of the formation of stable species with H2O and its hydrolysis products with O2-, and (3) a highly disordered, spectroscopically invisible Pu-Pu component. The structure and bonding in AnO(2+x) are therefore more complicated than have previously been assumed and show both similarities but also distinct differences among the different elements. (c) 2004 Elsevier Inc. All rights reserved.
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页码:521 / 535
页数:15
相关论文
共 44 条
[11]  
CONRADSON SD, 2004, IN PRESS J AM CHEM S
[12]  
CONRADSON SD, 2004, IN PRESS INORG CHEM
[13]   Structural and thermodynamic characterization of the perovskite-related Ba1+yUO3+x and (Ba, Sr)(1+y)UO3+x phases [J].
Cordfunke, EHP ;
Booij, AS ;
SmitGroen, V ;
vanVlaanderen, P ;
IJdo, DJW .
JOURNAL OF SOLID STATE CHEMISTRY, 1997, 131 (02) :341-349
[14]   BA2U2O7 - CRYSTAL-STRUCTURE AND PHASE-RELATIONSHIPS [J].
CORDFUNKE, EHP ;
IJDO, DJW .
JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 1988, 49 (05) :551-554
[15]   ON THE LATTICE OF BA3UO6 [J].
DEBLIECK, R ;
VANCAPPELLEN, E ;
VANTENDELOO, G ;
AMELINCKX, S ;
GENS, R ;
FUGER, J .
JOURNAL OF SOLID STATE CHEMISTRY, 1987, 68 (02) :375-378
[16]   POWDER NEUTRON-DIFFRACTION STUDY OF POTASSIUM URANATE(V), KUO3 [J].
DICKENS, PG ;
POWELL, AV .
JOURNAL OF MATERIALS CHEMISTRY, 1991, 1 (01) :137-138
[17]   Neptunium and plutonium solubilities in a Yucca Mountain groundwater [J].
Efurd, DW ;
Runde, W ;
Banar, JC ;
Janecky, DR ;
Kaszuba, JP ;
Palmer, PD ;
Roensch, FR ;
Tait, CD .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (24) :3893-3900
[18]   DECOMPOSITION, STOICHIOMETRY AND STRUCTURE OF NEPTUNIUM OXIDES [J].
FAHEY, JA ;
TURCOTTE, RP ;
CHIKALLA, TD .
JOURNAL OF INORGANIC & NUCLEAR CHEMISTRY, 1976, 38 (03) :495-500
[19]   Signatures of collective local and nanoscale distortions in diffraction experiments [J].
Garcia-Adeva, AJ ;
Conradson, DR ;
Villella, P ;
Conradson, SD .
JOURNAL OF PHYSICAL CHEMISTRY B, 2003, 107 (28) :6704-6716
[20]   Cuboctahedral oxygen clusters in U3O7 [J].
Garrido, F ;
Ibberson, RM ;
Nowicki, L ;
Willis, BTM .
JOURNAL OF NUCLEAR MATERIALS, 2003, 322 (01) :87-89