首页 | 本学科首页   官方微博 | 高级检索  
     

固溶处理对2205双相不锈钢组织及钝化膜特性的影响
引用本文:邢珊珊,戚浩宇,郑传波.固溶处理对2205双相不锈钢组织及钝化膜特性的影响[J].金属热处理,2020,45(3):146-150.
作者姓名:邢珊珊  戚浩宇  郑传波
作者单位:江苏科技大学 材料科学与工程学院, 江苏 镇江 212003
摘    要:用不同温度对2205双相不锈钢进行固溶处理,利用定量金相法及硬度法、电化学极化试验、电化学阻抗谱试验的方法研究固溶温度与2205双相不锈钢微观组织和钝化膜特性之间的关系。结果表明,当固溶温度为950 ℃时,有σ相存在,分布于铁素体/奥氏体晶界,当固溶温度为1000 ℃时,σ相消失,铁素体相比例随固溶温度的升高而升高,奥氏体相比例则呈相反规律;电化学试验和阻抗谱试验结果显示,材料在950 ℃时钝化膜稳定性和耐蚀性能最差,在1050 ℃时钝化膜稳定性和耐蚀性能最好。

关 键 词:2205双相不锈钢  固溶处理  显微组织  电化学  钝化膜  
收稿时间:2019-09-29

Effect of solution treatment on microstructure and passivation film properties of 2205 duplex stainless steel
Xing Shanshan,Qi Haoyu,Zheng Chuanbo.Effect of solution treatment on microstructure and passivation film properties of 2205 duplex stainless steel[J].Heat Treatment of Metals,2020,45(3):146-150.
Authors:Xing Shanshan  Qi Haoyu  Zheng Chuanbo
Affiliation:School of Materials Science and Engineering, Jiangsu University of Science and Technology, Zhenjiang Jiangsu 212003, China
Abstract:Solid solution treatment of 2205 duplex stainless steel was carried out at different temperatures.The relationship between solid solution temperature and microstructure and passivation film characteristics of 2205 duplex stainless steel was studied by means of quantitative metallographic method,hardness method,electrochemical polarization test and electrochemical impedance spectroscopy.The results show thatσphase exists at 950℃and distributes at ferrite/austenite grain boundaries,but disappears at 1000℃.Ferrite phase ratio increases with the increase of solid solution temperature,while austenite phase ratio shows the opposite rule.The electrochemical and impedance spectroscopy results show that the passivation film has the worst stability and corrosion resistance when solution treated at 950℃,and the passivation film has the best stability and corrosion resistance at 1050℃.
Keywords:2205 duplex stainless steel  solid solution treatment  microstructure  electrochemistry  passive film
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《金属热处理》浏览原始摘要信息
点击此处可从《金属热处理》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号