Development of an In Situ Micro-Corrosion Cell for the Investigation of Pitting Corrosion on Austenitic and Ferritic Stainless Steels

Sinan Kiremit, Julian Cremer, Yannic Stallmeier, Adrian Sonntag, Michaela Klöcker, D. Anselmetti, A. Hütten, T. Kordisch
{"title":"Development of an In Situ Micro-Corrosion Cell for the Investigation of Pitting Corrosion on Austenitic and Ferritic Stainless Steels","authors":"Sinan Kiremit, Julian Cremer, Yannic Stallmeier, Adrian Sonntag, Michaela Klöcker, D. Anselmetti, A. Hütten, T. Kordisch","doi":"10.3390/cmd4010007","DOIUrl":null,"url":null,"abstract":"In order to investigate the electrochemical pitting corrosion in more detail, a micro-corrosion cell was developed, allowing real-time in situ optical observations of steel surfaces in direct correlation with electrochemical measurement results. In this study, the austenitic 1.4301–X5CrNi18-10 and the ferritic 1.4016–X6Cr17 stainless steel grades were examined in electrolytes containing chloride ions. The micro-corrosion cell revealed a stable pitting corrosion of the ferritic 1.4016 and metastable pitting corrosion of the austenitic 1.4301. The pits were characterized by means of scanning electron microscopy (SEM) and atomic force microscopy (AFM) in detail. A clear correlation between current peaks in the current density-potential curve and the growth of many small pits on the test surface was established and was identified as metastable pit growth. In general, the pitting corrosion potential increased as the diameter of the test surface decreased for both stainless steels. In contrast to the complex precipitates of 1.4301, chromium precipitates with a significantly higher amount was detected on the entire surface of the 1.4016. The corrosion initiation was identified at the interface between the precipitates and the base material for both stainless steels. By comparing both materials, the ferritic 1.4016 had a lower pitting corrosion potential than the austenitic 1.4301 under all test conditions.","PeriodicalId":10693,"journal":{"name":"Corrosion and Materials Degradation","volume":"11 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Corrosion and Materials Degradation","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/cmd4010007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

In order to investigate the electrochemical pitting corrosion in more detail, a micro-corrosion cell was developed, allowing real-time in situ optical observations of steel surfaces in direct correlation with electrochemical measurement results. In this study, the austenitic 1.4301–X5CrNi18-10 and the ferritic 1.4016–X6Cr17 stainless steel grades were examined in electrolytes containing chloride ions. The micro-corrosion cell revealed a stable pitting corrosion of the ferritic 1.4016 and metastable pitting corrosion of the austenitic 1.4301. The pits were characterized by means of scanning electron microscopy (SEM) and atomic force microscopy (AFM) in detail. A clear correlation between current peaks in the current density-potential curve and the growth of many small pits on the test surface was established and was identified as metastable pit growth. In general, the pitting corrosion potential increased as the diameter of the test surface decreased for both stainless steels. In contrast to the complex precipitates of 1.4301, chromium precipitates with a significantly higher amount was detected on the entire surface of the 1.4016. The corrosion initiation was identified at the interface between the precipitates and the base material for both stainless steels. By comparing both materials, the ferritic 1.4016 had a lower pitting corrosion potential than the austenitic 1.4301 under all test conditions.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
用于研究奥氏体和铁素体不锈钢点蚀的原位微腐蚀池的研制
为了更详细地研究电化学点蚀,开发了一种微腐蚀电池,可以实时地对钢表面进行原位光学观察,并与电化学测量结果直接相关。本研究在含氯离子电解质中对奥氏体1.4301-X5CrNi18-10和铁素体1.4016-X6Cr17不锈钢牌号进行了研究。微腐蚀池表现为铁素体1.4016的稳定点蚀和奥氏体1.4301的亚稳点蚀。利用扫描电子显微镜(SEM)和原子力显微镜(AFM)对凹坑进行了详细的表征。电流密度-电位曲线上的电流峰值与测试表面上许多小凹坑的生长之间存在明显的相关性,并将其确定为亚稳凹坑生长。总的来说,两种不锈钢的点蚀电位随着测试表面直径的减小而增加。与1.4301的复合析出相相比,在1.4016的整个表面检测到的铬析出相数量明显更高。两种不锈钢的腐蚀起始点均在析出相与基体之间的界面处。通过对比两种材料,在所有测试条件下,铁素体1.4016的点蚀电位都低于奥氏体1.4301。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
4.50
自引率
0.00%
发文量
0
期刊最新文献
Influence of Isothermal Annealing in the 600 to 750 °C Range on the Degradation of SAF 2205 Duplex Stainless Steel Unraveling the Corrosion of the Ti–6Al–4V Orthopedic Alloy in Phosphate-Buffered Saline (PBS) Solution: Influence of Frequency and Potential Impact of the Delay Period between Electrochemical Hydrogen Charging and Tensile Testing on the Mechanical Properties of Mild Steel Mechanistic Analysis of Hydrogen Evolution Reaction on Stationary Polycrystalline Gold Electrodes in H2SO4 Solutions In-Situ AFM Studies of Surfactant Adsorption on Stainless Steel Surfaces during Electrochemical Polarization
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1