Corrosion of carbon steel and the passivating properties of corrosion films formed under high-PT geothermal conditions

被引:18
作者
Mundhenk, Niklas [1 ]
Knauss, Kevin G. [1 ]
Bandaru, Siva R. S. [2 ]
Wonneberger, Robert [3 ]
Devine, Thomas M. [2 ]
机构
[1] Lawrence Berkeley Natl Lab, Energy Geosci Div, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Berkeley, CA 94720 USA
[3] Friedrich Schiller Univ Jena, Otto Schott Inst Mat Res, D-07743 Jena, Germany
关键词
CO2; CORROSION; MILD-STEEL; IRON; IMPEDANCE; MECHANISM; BEHAVIOR; ELECTROCHEMISTRY; STABILITY; ALLOYS; ANIONS;
D O I
10.1016/j.scitotenv.2019.04.386
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Corrosion is a major obstacle to a safe implementation of geotechnical applications. Using a novel approach that includes vertical scanning interferometry (VSI) and electrochemical impedance spectroscopy (EIS) we discuss time-dependent carbon steel corrosion and film formation at geothermally relevant temperatures (80-160 degrees C) in CO2-saturated mildly acidic Na-Cl brine. Iron dissolution kinetics follows a logarithmic rate at 80 and 160 degrees C and a linear rate at 120 degrees C. At 80 degrees C, high initial corrosion rates (first 24 h) generate H-2 at a minimum rate of 12 mu mol h(-1) cm(-2) and lead to the formation of a continuous similar to 100 mu m thick porous corrosion film. It exhibits a duplex structure with a crystalline outer FeCO3 layer and an inner layer composed of a skeletal network of Fe3C impregnated with FeCO3. Being an electrical conductor we hypothesize the Fe3C to strongly enhance corrosion rates by providing additional cathodic sites. Pseudo-passivity due to an anodic film-forming reaction (presumably Fe-oxide) was observed at 120 and 160 degrees C, soon followed by the initiation of pitting at 120 degrees C. Steady-state corrosion rates at 160 degrees C are at least one order of magnitude lower than for 120 degrees C. Our experimental approach demonstrated potential for general applicability in studying corrosion-related phenomena. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:307 / 314
页数:8
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