Mariana Georges , Ramgopal Thodla , Sirui Li , Christopher Taylor , Narasi Sridhar , Gerald S. Frankel
{"title":"Ni600和SS304在SCC条件下的局部腐蚀和再钝化行为","authors":"Mariana Georges , Ramgopal Thodla , Sirui Li , Christopher Taylor , Narasi Sridhar , Gerald S. Frankel","doi":"10.1016/j.corsci.2025.113254","DOIUrl":null,"url":null,"abstract":"<div><div>In this study, the corrosion kinetics and repassivation behavior of stainless steel 304 (SS304) and nickel alloy 600 (Alloy 600) were investigated and compared under pit and crack-like environments. The corrosion kinetics of nickel Alloy 270 (pure nickel) was also assessed for reference. To evaluate the kinetics of metal dissolution under aggressive conditions, downward potential scans were performed on one-dimensional (1D) pit samples. These scans were used to determine the dissolution current density across a range of temperatures at a fixed metal cation concentration at the metal surface corresponding to the saturation level at 20 °C (C<sub>sat_20</sub>). Repassivation behavior was evaluated using constant potential and constant temperature tests. In the first approach, downward potential scans at 25 °C were employed to identify the potential and pit depth at which repassivation occurs for each alloy. In the second method, downward temperature scans under constant applied potential were used to assess the corresponding temperature and pit depth at repassivation. Under charge-transfer-controlled conditions, pure nickel exhibits the slowest dissolution kinetics, followed by Alloy 600, with SS304 exhibiting the fastest rate. However, SS304 demonstrates a greater tendency to repassivate compared to Alloy 600. The critical concentration for repassivation was 60 % of the saturation concentration for SS304 and 15 % for Alloy 600. Density Functional Theory simulations provided mechanistic insights into these observations. A mechanistic explanation of the effects of electrochemistry on stress corrosion cracking resistance of Ni- and Fe-based alloys was proposed.</div></div>","PeriodicalId":290,"journal":{"name":"Corrosion Science","volume":"257 ","pages":"Article 113254"},"PeriodicalIF":7.4000,"publicationDate":"2025-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Localized corrosion and repassivation behavior of Ni600 and SS304 under conditions relevant to SCC\",\"authors\":\"Mariana Georges , Ramgopal Thodla , Sirui Li , Christopher Taylor , Narasi Sridhar , Gerald S. Frankel\",\"doi\":\"10.1016/j.corsci.2025.113254\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In this study, the corrosion kinetics and repassivation behavior of stainless steel 304 (SS304) and nickel alloy 600 (Alloy 600) were investigated and compared under pit and crack-like environments. The corrosion kinetics of nickel Alloy 270 (pure nickel) was also assessed for reference. To evaluate the kinetics of metal dissolution under aggressive conditions, downward potential scans were performed on one-dimensional (1D) pit samples. These scans were used to determine the dissolution current density across a range of temperatures at a fixed metal cation concentration at the metal surface corresponding to the saturation level at 20 °C (C<sub>sat_20</sub>). Repassivation behavior was evaluated using constant potential and constant temperature tests. In the first approach, downward potential scans at 25 °C were employed to identify the potential and pit depth at which repassivation occurs for each alloy. In the second method, downward temperature scans under constant applied potential were used to assess the corresponding temperature and pit depth at repassivation. Under charge-transfer-controlled conditions, pure nickel exhibits the slowest dissolution kinetics, followed by Alloy 600, with SS304 exhibiting the fastest rate. However, SS304 demonstrates a greater tendency to repassivate compared to Alloy 600. The critical concentration for repassivation was 60 % of the saturation concentration for SS304 and 15 % for Alloy 600. Density Functional Theory simulations provided mechanistic insights into these observations. A mechanistic explanation of the effects of electrochemistry on stress corrosion cracking resistance of Ni- and Fe-based alloys was proposed.</div></div>\",\"PeriodicalId\":290,\"journal\":{\"name\":\"Corrosion Science\",\"volume\":\"257 \",\"pages\":\"Article 113254\"},\"PeriodicalIF\":7.4000,\"publicationDate\":\"2025-08-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Corrosion Science\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0010938X25005815\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Corrosion Science","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0010938X25005815","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
Localized corrosion and repassivation behavior of Ni600 and SS304 under conditions relevant to SCC
In this study, the corrosion kinetics and repassivation behavior of stainless steel 304 (SS304) and nickel alloy 600 (Alloy 600) were investigated and compared under pit and crack-like environments. The corrosion kinetics of nickel Alloy 270 (pure nickel) was also assessed for reference. To evaluate the kinetics of metal dissolution under aggressive conditions, downward potential scans were performed on one-dimensional (1D) pit samples. These scans were used to determine the dissolution current density across a range of temperatures at a fixed metal cation concentration at the metal surface corresponding to the saturation level at 20 °C (Csat_20). Repassivation behavior was evaluated using constant potential and constant temperature tests. In the first approach, downward potential scans at 25 °C were employed to identify the potential and pit depth at which repassivation occurs for each alloy. In the second method, downward temperature scans under constant applied potential were used to assess the corresponding temperature and pit depth at repassivation. Under charge-transfer-controlled conditions, pure nickel exhibits the slowest dissolution kinetics, followed by Alloy 600, with SS304 exhibiting the fastest rate. However, SS304 demonstrates a greater tendency to repassivate compared to Alloy 600. The critical concentration for repassivation was 60 % of the saturation concentration for SS304 and 15 % for Alloy 600. Density Functional Theory simulations provided mechanistic insights into these observations. A mechanistic explanation of the effects of electrochemistry on stress corrosion cracking resistance of Ni- and Fe-based alloys was proposed.
期刊介绍:
Corrosion occurrence and its practical control encompass a vast array of scientific knowledge. Corrosion Science endeavors to serve as the conduit for the exchange of ideas, developments, and research across all facets of this field, encompassing both metallic and non-metallic corrosion. The scope of this international journal is broad and inclusive. Published papers span from highly theoretical inquiries to essentially practical applications, covering diverse areas such as high-temperature oxidation, passivity, anodic oxidation, biochemical corrosion, stress corrosion cracking, and corrosion control mechanisms and methodologies.
This journal publishes original papers and critical reviews across the spectrum of pure and applied corrosion, material degradation, and surface science and engineering. It serves as a crucial link connecting metallurgists, materials scientists, and researchers investigating corrosion and degradation phenomena. Join us in advancing knowledge and understanding in the vital field of corrosion science.