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(Gd,Y)相对GW103K时效合金局部腐蚀的影响
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  • 英文篇名:Effect of(Gd,Y) Containing-phases on Local Corrosion of Aged GW103K Alloy
  • 作者:于爽 ; 贾瑞灵 ; 张函 ; 张伟 ; 郭锋
  • 英文作者:YU Shuang;JIA Ruiling;ZHANG Han;ZHANG Wei;GUO Feng;School of Materials Science and Engineering, Inner Mongolia University of Technology, Key Laboratory of Film and Coating in Inner Mongolia;Laboratory for Corrosion and Protection, Institute of Metal Research, Chinese Academy of Sciences;
  • 关键词:金属材料 ; 镁合金 ; 腐蚀微电偶 ; SKPFM ; (Gd ; Y)相 ; 相对电势
  • 英文关键词:metallic materials;;Mg alloy;;corrosion micro-galvanic;;SKPFM;;(Gd,Y) phase;;relative potential
  • 中文刊名:CYJB
  • 英文刊名:Chinese Journal of Materials Research
  • 机构:内蒙古工业大学材料科学与工程学院内蒙古薄膜与涂层重点实验室;中国科学院金属研究所金属腐蚀与防护实验室;
  • 出版日期:2019-03-25
  • 出版单位:材料研究学报
  • 年:2019
  • 期:v.33
  • 基金:内蒙古自然科学基金(2016MS0538);; STS计划配套(2016T3030)~~
  • 语种:中文;
  • 页:CYJB201903006
  • 页数:10
  • CN:03
  • ISSN:21-1328/TG
  • 分类号:41-50
摘要
对Mg-10Gd-3Y-0.4Zr(GW103K)合金进行193 h时效处理,使用扫描电子显微镜(SEM)和透射电子显微镜(TEM)观测块状和链状相的微观结构和腐蚀形貌,使用扫描开尔文探针显微镜(SKPFM)测试块状相和链状相与基体之间的相对电势差,研究了这些相对GW103K合金局部腐蚀的影响。结果表明:分布在晶内和晶界的单独块状相为Mg2(Gd, Y)相,(Gd, Y)固溶体与Mg2(Gd, Y)相交替排列形成链状相。(Gd, Y)固溶体和Mg2(Gd, Y)相的相对电势均高于基体,与相邻基体形成微电池,(Gd, Y)固溶体和Mg2(Gd, Y)相作为阴极促进了周围基体的腐蚀。尽管(Gd,Y)固溶体与基体之间的相对电势差更大,但是与基体的相界面为共格界面,界面能低、化学稳定性高,因此对基体腐蚀没有更强烈的影响。
        The cast Mg-10 Gd-3 Y-0.4 Zr(GW103 K) alloy was solution treated at 500 oC for 4 h and then aged at 225℃ for 193 h. The microstructure and corrosion performance in NaCl solution of the alloy were assessed by means of scanning electron microscope(SEM), transmission electron microscope(TEM), immersion test and scanning Kelvin probe atomic force microscope(SKPFM). The results show that the alloy shows a microstructure composed of α-Mg matrix with bulk-like Mg2(Gd, Y) phase and chain-like structure of alternatively arranged phases of(Gd,Y) solid solution and Mg2(Gd, Y), while the later two phases distributed in grains and/or at grain boundaries. The free corrosion potentials of the two phases(Gd, Y) solid solution and bulk-like Mg2(Gd, Y) are nobler than that of the α-Mg matrix, thereby the micro-galvanic coupling could form between the former phases with the α-Mg matrix. The(Gd, Y) solid solution and bulk-like Mg2(Gd, Y) acted as micro-cathodes to promote the corrosion of the surrounding matrix. It is worthy noted that even though the relative potential difference between the(Gd, Y) solid solution and the α-Mg matrix is greater, however, the interface between the(Gd, Y) solid solution and α-Mg matrix is coherent and the interfacial energy of the two phases is lower, thus they may exhibit better chemical compatibility, as a result, the(Gd, Y) solid solution phase may have little influence on the matrix corrosion.
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