{"title":"Inhibition of corrosion mechanism of Cl− in 304 stainless steel by different SO42− concentration at 30 °C","authors":"Xin Zhang, Xinyue Liu, Yonglong Wu, Xiaoqiang Li, Xiaoxiao Duan, Yongsheng Ren","doi":"10.1016/j.matchemphys.2025.130979","DOIUrl":null,"url":null,"abstract":"<div><div>The development of passivation layer and characterization of pitting formation on the surface of 304 stainless steel (SS) in solutions containing different concentrations of 0.38 M Cl<sup>−</sup> were investigated. Electrochemical methods, Mott-Schottky analysis, XPS, pitting growth analysis and surface morphology characterization were used in the study. The results show that an increase in the concentration of SO<sub>4</sub><sup>2−</sup> at 0, 0.097 M, 0.106 M, and 0.113 M leads to an increase in corrosion potential, breakdown potential, and a decrease in corrosion current density, whereas a change in the concentration of SO<sub>4</sub><sup>2−</sup> inhibits the corrosion reaction and pitting growth of Cl<sup>−</sup> on stainless steel. In the presence of sulfate ions, a sulfate film forms on the top of the passivation film due to the interaction between SO<sub>4</sub><sup>2−</sup> and the metal cations. The adsorption of SO<sub>4</sub><sup>2−</sup> on the surface of the sample replaces some of the Cl<sup>−</sup>, reducing the oxygen vacancies available for the adsorption of Cl<sup>−</sup> and lowering the carrier density. At the bottom of the crater, the large amount of SO<sub>4</sub><sup>2−</sup> adsorption prevents the penetration of Cl<sup>−</sup>, thus inhibiting the growth of the pitting craters.</div></div>","PeriodicalId":18227,"journal":{"name":"Materials Chemistry and Physics","volume":"343 ","pages":"Article 130979"},"PeriodicalIF":4.3000,"publicationDate":"2025-05-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Chemistry and Physics","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S025405842500625X","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
The development of passivation layer and characterization of pitting formation on the surface of 304 stainless steel (SS) in solutions containing different concentrations of 0.38 M Cl− were investigated. Electrochemical methods, Mott-Schottky analysis, XPS, pitting growth analysis and surface morphology characterization were used in the study. The results show that an increase in the concentration of SO42− at 0, 0.097 M, 0.106 M, and 0.113 M leads to an increase in corrosion potential, breakdown potential, and a decrease in corrosion current density, whereas a change in the concentration of SO42− inhibits the corrosion reaction and pitting growth of Cl− on stainless steel. In the presence of sulfate ions, a sulfate film forms on the top of the passivation film due to the interaction between SO42− and the metal cations. The adsorption of SO42− on the surface of the sample replaces some of the Cl−, reducing the oxygen vacancies available for the adsorption of Cl− and lowering the carrier density. At the bottom of the crater, the large amount of SO42− adsorption prevents the penetration of Cl−, thus inhibiting the growth of the pitting craters.
期刊介绍:
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