Electrochemical and Raman spectroscopic studies of the influence of chlorinated solvents on the corrosion behaviour of iron in borate buffer and in simulated groundwater

被引:56
作者
Bonin, PML [1 ]
Jedral, W
Odziemkowski, MS
Gillham, RW
机构
[1] Univ Waterloo, Dept Earth Sci, Waterloo, ON N2L 3G1, Canada
[2] Univ Warsaw, Dept Chem, PL-02093 Warsaw, Poland
基金
加拿大自然科学与工程研究理事会;
关键词
iron; borate buffer; calcium carbonate; potassium bromide; carbon tetrachloride; corrosion potential; corrosion rate; Raman spectroscopy; green rust; iron oxides;
D O I
10.1016/S0010-938X(00)00027-5
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The remediation, by contact with granular iron, of groundwater contaminated with chlorinated halocarbons necessitates a flow of electrons at the iron/solution interface. To refine our understanding of the mechanism and kinetics of the charge transfer process, electrochemical and spectroscopic measurements were performed on iron electrodes in borate buffer and in simulated groundwater solutions of calcium carbonate and potassium bromide, before and after exposure to carbon tetrachloride. The results of these measurements highlighted the combined influence of the organic contaminant and inorganic ions on the corrosion behaviour of iron as well as on the nature of the films formed in their presence. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1921 / 1939
页数:19
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