Accelerated cathodic reaction in microbial corrosion of iron due to direct electron uptake by sulfate-reducing bacteria

被引：388

作者：

Venzlaff, Hendrik ^{[1
]}

Enning, Dennis ^{[2
]}

Srinivasan, Jayendran ^{[1
]}

Mayrhofer, Karl J. J. ^{[1
]}

Hassel, Achim Walter ^{[3
]}

Widdel, Friedrich ^{[2
]}

Stratmann, Martin ^{[1
]}

机构：

[1] Max Planck Inst Iron Res, D-40237 Dusseldorf, Germany

[2] Max Planck Inst Marine Microbiol, D-28359 Bremen, Germany

[3] Johannes Kepler Univ Linz, Inst Chem Technol Inorgan Mat, A-4040 Linz, Austria

来源：

CORROSION SCIENCE | 2013年 / 66卷

关键词：

Iron; Polarization; EIS; Microbiological corrosion; MILD-STEEL; HYDROGEN; BIOFILM; POLARIZATION; REDUCTION; NANOWIRES; CULTURES; ECOLOGY;

D O I：

10.1016/j.corsci.2012.09.006

中图分类号：

T [工业技术];

学科分类号：

08 ;

摘要：

Microbially influenced iron corrosion by sulfate-reducing bacteria (SRB) is conventionally attributed to the chemical corrosiveness of H2S, facilitated abiotic H+-eduction at deposited FeS, and biological consumption of chemically formed ('cathodic') H-2. However, recent studies with corrosive SRB indicated direct consumption of iron-derived electrons rather than of H-2 as a crucial mechanism. Here, we conducted potentiodynamic measurements with iron electrodes colonized by corrosive SRB. They significantly stimulated the cathodic reaction, while non-corrosive yet H-2-consuming control SRB had no effect. Inactivation of the colonizing bacteria significantly reduced current stimulation, thus confirming biological catalysis rather than an abiotic cathodic effect of FeS. (c) 2012 Elsevier Ltd. All rights reserved.

引用

页码：88 / 96

页数：9

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