Transition of interface oxide layer from porous Mg(OH)2 to dense MgO induced by polyaniline and corrosion resistance of Mg alloy therefrom

被引:56
作者
Luo, Yizhong [1 ,2 ]
Sun, Yang [1 ]
Lv, Jinlong [1 ]
Wang, Xianhong [1 ]
Li, Ji [1 ]
Wang, Fosong [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, Key Lab Polymer Ecomat, Changchun 130022, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
Polyaniline; Magnesium alloy; Corrosion resistance; Interface oxide layer; MICRO-ARC OXIDATION; MAGNESIUM ALLOYS; ANTICORROSION PROPERTIES; STAINLESS-STEEL; EMERALDINE BASE; PROTECTION; COATINGS; BEHAVIOR; FILM; AZ91;
D O I
10.1016/j.apsusc.2014.11.177
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The feasibility of polyaniline emeraldine base (EB) for enhancing long-term corrosion resistance of magnesium alloy (AZ91D Mg alloy) was confirmed, since the complex impedance of Mg alloy protected by EB/epoxy resin (ER) composite coating with 10 wt% EB loading maintained around 2 GSZ cm(2) even after 80 day exposure in 0.5 M NaCl solution, while that of pure ER coated analogue decreased to 0.17 M Omega cm(2) only after 31 days. The improvement in corrosion resistance was attributed to the transition of interface layer from porous Mg(OH)(2) dominated one underneath pure ER coating to dense MgO dominated one underneath EB/ER coating, induced by the redox interaction of EB with Mg alloy. When the EB loading in EB/ER coating increased from 0 to 10 wt%, the relative XPS peak area ratio of MgO to Mg(OH)(2) increased from 0.78 to 1.18, indicating that EB behaved as effective corrosion inhibitor causing the transformation of oxide layer from porous Mg(OH)(2) to dense MgO. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:247 / 254
页数:8
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