Surface electrochemistry of UO2 in dilute alkaline hydrogen peroxide solutions

被引:47
|
作者
Goldik, JS
Nesbitt, HW
Noël, JJ
Shoesmith, DW [1 ]
机构
[1] Univ Western Ontario, Dept Chem, London, ON N6A 5B7, Canada
[2] Univ Western Ontario, Dept Earth Sci, London, ON N6A 5B7, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
uranium dioxide; hydrogen peroxide; cyclic voltammetry; corrosion potential; nuclear waste disposal;
D O I
10.1016/j.electacta.2003.11.029
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The reaction of H2O2 on SIMFUEL electrodes has been studied electrochemically and under open circuit conditions in 0.1 mol l(-1) NaCl (pH 9.8). The composition of the oxidized UO2 Surface was determined by X-ray photoelectron spectroscopy (XPS). Peroxide reduction was found to be catalyzed by the formation of a mixed U-IV/U-V (UO2+x) surface layer, but to be blocked by the formation of U-VI (UO22+) species on the electrode surface. The formation of this U-VI layer blocks both H2O2 reduction and oxidation, thereby inhibiting the potentially rapid H2O2 decomposition process to H2O and O-2. Decomposition is found to proceed at a rate controlled by desorption or reduction of the adsorbed O-2 species. Reduction of O-2 is coupled to the slow oxidative dissolution of UO2 and formation of a corrosion product deposit of UO3.yH(2)O. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1699 / 1709
页数:11
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