Corrosion of Mg alloys EV31A, WE43B, and ZE41A in chloride- and sulfate-containing solutions saturated with magnesium hydroxide

被引:21
|
作者
Soltan, Akif [1 ,2 ]
Dargusch, Matthew S. [1 ,2 ]
Shi, Zhiming [1 ,2 ]
Gerrard, Darren [3 ]
Al Shabibi, Sulaiman [1 ]
Kuo, Yu-Chieh [1 ]
Atrens, Andrej [1 ]
机构
[1] Univ Queensland, Sch Mech & Min Engn, Brisbane, Qld 4072, Australia
[2] Def Mat Technol Ctr DMTC Ltd, Hawthorn, Vic, Australia
[3] Def Sci & Technol Grp, Melbourne, Vic, Australia
来源
关键词
EIS; hydrogen evolution; magnesium; polarization; SEM; ELECTROMAGNETIC SHIELDING EFFECTIVENESS; ENHANCED CATALYTIC-ACTIVITY; HIGH-PURITY MG; MECHANICAL-PROPERTIES; HYDROGEN EVOLUTION; ELECTROCHEMICAL-BEHAVIOR; ANODIC-DISSOLUTION; RARE-EARTH; LOCALIZED CORROSION; SURFACE-FILM;
D O I
10.1002/maco.201911375
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
This study studied corrosion in 0.1 M Na2SO4, 0.1 M NaCl, and 0.6 M NaCl, all saturated with Mg(OH)(2), using weight loss, hydrogen evolution, and electrochemical measurements. Corrosion was similar in all cases. Nevertheless, the corrosion rates were alloy-dependent, were somewhat lower in 0.1 M Na2SO4 than in 0.1 M NaCl, and increased with NaCl concentration. The corrosion damage morphology was similar for all solutions; the extent correlated with the corrosion rate. The corrosion rates evaluated by the electrochemical methods were lower than those evaluated from hydrogen evolution, consistent with the Mg corrosion mechanism involving the unipositive Mg+ ion.
引用
收藏
页码:956 / 979
页数:24
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