Oxidation state determination of plutonium aquo ions using x-ray absorption spectroscopy

被引:62
|
作者
Conradson, SD
Al Mahamid, I
Clark, DL
Hess, NJ
Hudson, EA
Neu, MP
Palmer, PD
Runde, WH
Tait, CD
机构
[1] Los Alamos Natl Lab, Chem Sci & Technol Div, Los Alamos, NM 87545 USA
[2] Los Alamos Natl Lab, Div Mat Sci & Technol, Los Alamos, NM 87545 USA
[3] Lawrence Berkeley Lab, Berkeley, CA 94550 USA
[4] GT Seaborg Inst Transactinium Sci, Livermore, CA USA
[5] Pacific NW Lab, Dept Mat Sci, Richland, WA 99352 USA
关键词
XANES; plutonium; oxidation state;
D O I
10.1016/S0277-5387(97)00287-8
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Four oxidation states (III, IV, V, and VI) of Pu may coexist under environmentally relevant conditions. An efficient method to determine the states actually present in various matrices would enhance the ability to model the fate and transport of plutonium in process streams and in the environment. This communication establishes that the L-3 X-ray absorption near-edge structure (XANES) spectra of Pu are primarily determined by the valence state and the presence or absence of the trans dioxo moiety, consistent with previous U and Np XANES studies. The edge energies were observed to shift progressively to higher energy with increasing valence, with an average 1.68 eV increase per formal oxidation state increase. Ih addition, the general spectral shape of the (III) and (IV) species is clearly different from the dioxo-containing (V) and (VI) species, with the first maximum much larger and sharper for the (III) and (IV) spectra than for the (V) and (VI) spectra. (C) 1998 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:599 / 602
页数:4
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