Grazing incidence XAFS spectroscopy of uranyl sorbed onto TiO2 rutile surfaces

被引:68
作者
Den Auwer, C [1 ]
Drot, R
Simoni, E
Conradson, SD
Gailhanou, M
de Leon, JM
机构
[1] Univ Paris Sud Orsay, Inst Phys Nucl, F-91405 Orsay, France
[2] CEA Marcoule DEN, DRCP, SCPS, F-30207 Bagnols Sur Ceze, France
[3] Los Alamos Natl Lab, MST Div, Los Alamos, NM 87545 USA
[4] Univ Paris Sud Orsay, Lab Utilisat Rayonnement Electromagnet, F-91898 Orsay, France
[5] CINVESTAV, Dept Fis Aplicada, Mexico City 97310, DF, Mexico
关键词
D O I
10.1039/b209961f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The surface complex formed by uranyl oxocations sorbed onto rutile titanium oxide has been probed by X-ray Absorption Spectroscopy. These measurements are part of a work that aims to model the interaction between heavy metal ions and mineral surfaces in aqueous conditions. In order to de ne the orientation and structure of the oxocation complex on the surface, both polycrystalline and monocrystalline ( 110) and (001) planes of rutile TiO2 have been investigated. Polarized XANES measurements show that the uranyl rod sorbs nearly parallel to the rutile surface, although this ideal configuration must be modulated by the surface topographic defects. Site by site simulation compared to the EXAFS data suggests that two surface oxygen sites are involved: shared edge and shared summit oxygen atoms of the TiO6 octahedron. Both grazing incidence EXAFS on the ( 110) plane and isotropic EXAFS on polycrystalline TiO2 reveal comparable sorption behavior: on average, the uranyl oxocation bonds to the surface as a bidentate complex with two short oxygen distances at 2.32 Angstrom and three larger distances at 2.47 Angstrom. Grazing incidence EXAFS on the ( 001) plane shows an unexpected low signal to noise ratio due to the lower uranium uptake. Data analysis suggests the formation of an outer sphere uranium complex on this plane. The discrepancy between both plane reactivities is still not understood.
引用
收藏
页码:648 / 655
页数:8
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