Crystal-orientation-dependent corrosion behaviour of single crystals of a pure Mg and Mg-Al and Mg-Cu solid solutions

被引:144
作者
Hagihara, Koji [1 ]
Okubo, Masayoshi [1 ]
Yamasaki, Michiaki [2 ,3 ,4 ]
Nakano, Takayoshi [5 ]
机构
[1] Osaka Univ, Grad Sch Engn, Dept Adapt Machine Syst, 2-1 Yamadaoka, Suita, Osaka 5650871, Japan
[2] Univ Queensland, Sch Mech & Min Engn, Brisbane, Qld 4072, Australia
[3] Kumamoto Univ, Magnesium Res Ctr, Chuo Ku, 2-39-1 Kurokami, Kumamoto 8608555, Japan
[4] Kumamoto Univ, Dept Mat Sci, Chuo Ku, 2-39-1 Kurokami, Kumamoto 8608555, Japan
[5] Osaka Univ, Grad Sch Engn, Div Mat & Mfg Sci, 2-1 Yamadaoka, Suita, Osaka 5650871, Japan
基金
日本学术振兴会;
关键词
Magnesium; Electrochemical impedance spectroscopy (EIS); Polarization; HIGH-PURITY MG; CRYSTALLOGRAPHIC ORIENTATION; ELECTROCHEMICAL CORROSION; IN-VITRO; INTERMETALLIC COMPOUNDS; MAGNESIUM CORROSION; HYDROGEN EVOLUTION; ANODIC-DISSOLUTION; NACL SOLUTION; ALLOYS;
D O I
10.1016/j.corsci.2016.03.019
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Mg alloys are promising candidates for biodegradable materials. To control their dissolution rate, the orientation-dependent corrosion behaviour of pure-Mg single crystals was examined. The corrosion rates increased in the order (0001) < (11<(2)over bar>0) < (10<(1)over bar>0) < (11<(2)over bar>3) < (10<(1)over bar>2). We found the anodic reaction governs the orientation-dependent corrosion behaviour. The charge-transfer and film resistances were strongly orientation-dependent. Effects of Al or Cu-addition to the orientation-dependent corrosion behaviour were also examined as model materials. Al-addition promoted passivation in anodic polarization, while Cu-addition activated the cathodic reaction. However, neither Al nor Cu influenced the order of orientation-dependent corrosion behaviour. Such orientation-dependence may originate from the variation in surface atomic-packing density. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:68 / 85
页数:18
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