{"title":"氢在NaCl溶液中进入镀锌钢的原位二维可视化:锌溶解和电位分布的作用","authors":"Hiroshi Kakinuma , Saya Ajito , Koki Okumura , Makoto Akahoshi , Yu Takabatake , Tomohiko Omura , Motomichi Koyama , Eiji Akiyama","doi":"10.1016/j.corsci.2025.113386","DOIUrl":null,"url":null,"abstract":"<div><div>The hydrogen entry behavior of a partially Zn-coated steel sheet in NaCl solutions was investigated employing a polyaniline-based hydrogenochromic sensor, electrochemical hydrogen permeation tests, and potential measurements using a scanning Kelvin probe. While the Zn coating mitigated corrosion of the steel substrate, it simultaneously accelerated the hydrogen entry. The hydrogen entry occurred at the bare steel surface regions exposed to the NaCl solution, with the hydrogen flux exhibiting non-uniform distribution: higher near the dissolving Zn coating. While no significant differences in Zn dissolution behavior or galvanic current were observed between 0.1 and 0.01 M NaCl solutions, the total hydrogen flux decreased with decreasing Cl<sup>−</sup> concentration. This reduction was attributed to a potential gradient induced by differences in electrolyte conductivity. The results demonstrate that potential distribution, rather than galvanic current, is a dominant factor influencing hydrogen entry under the investigated conditions.</div></div>","PeriodicalId":290,"journal":{"name":"Corrosion Science","volume":"258 ","pages":"Article 113386"},"PeriodicalIF":7.4000,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"In situ 2D visualization of hydrogen entry into Zn-coated steels in NaCl solutions: Roles of Zn dissolution and potential distribution\",\"authors\":\"Hiroshi Kakinuma , Saya Ajito , Koki Okumura , Makoto Akahoshi , Yu Takabatake , Tomohiko Omura , Motomichi Koyama , Eiji Akiyama\",\"doi\":\"10.1016/j.corsci.2025.113386\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The hydrogen entry behavior of a partially Zn-coated steel sheet in NaCl solutions was investigated employing a polyaniline-based hydrogenochromic sensor, electrochemical hydrogen permeation tests, and potential measurements using a scanning Kelvin probe. While the Zn coating mitigated corrosion of the steel substrate, it simultaneously accelerated the hydrogen entry. The hydrogen entry occurred at the bare steel surface regions exposed to the NaCl solution, with the hydrogen flux exhibiting non-uniform distribution: higher near the dissolving Zn coating. While no significant differences in Zn dissolution behavior or galvanic current were observed between 0.1 and 0.01 M NaCl solutions, the total hydrogen flux decreased with decreasing Cl<sup>−</sup> concentration. This reduction was attributed to a potential gradient induced by differences in electrolyte conductivity. The results demonstrate that potential distribution, rather than galvanic current, is a dominant factor influencing hydrogen entry under the investigated conditions.</div></div>\",\"PeriodicalId\":290,\"journal\":{\"name\":\"Corrosion Science\",\"volume\":\"258 \",\"pages\":\"Article 113386\"},\"PeriodicalIF\":7.4000,\"publicationDate\":\"2025-10-10\",\"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/S0010938X25007140\",\"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/S0010938X25007140","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}
引用次数: 0
摘要
采用基于聚苯胺的氢致变色传感器、电化学氢渗透测试和扫描开尔文探针的电位测量,研究了部分镀锌钢板在NaCl溶液中的氢进入行为。镀锌层在减缓钢基体腐蚀的同时,也加速了氢的进入。氢的进入主要发生在裸露的钢表面NaCl溶液中,且氢通量分布不均匀,靠近溶解的Zn涂层处氢通量较高。在0.1和0.01 M NaCl溶液中,锌的溶解行为和电流无显著差异,但总氢通量随着Cl−浓度的降低而降低。这种减少归因于电解质电导率差异引起的电位梯度。结果表明,在实验条件下,影响氢气进入的主要因素不是电流,而是电势分布。
In situ 2D visualization of hydrogen entry into Zn-coated steels in NaCl solutions: Roles of Zn dissolution and potential distribution
The hydrogen entry behavior of a partially Zn-coated steel sheet in NaCl solutions was investigated employing a polyaniline-based hydrogenochromic sensor, electrochemical hydrogen permeation tests, and potential measurements using a scanning Kelvin probe. While the Zn coating mitigated corrosion of the steel substrate, it simultaneously accelerated the hydrogen entry. The hydrogen entry occurred at the bare steel surface regions exposed to the NaCl solution, with the hydrogen flux exhibiting non-uniform distribution: higher near the dissolving Zn coating. While no significant differences in Zn dissolution behavior or galvanic current were observed between 0.1 and 0.01 M NaCl solutions, the total hydrogen flux decreased with decreasing Cl− concentration. This reduction was attributed to a potential gradient induced by differences in electrolyte conductivity. The results demonstrate that potential distribution, rather than galvanic current, is a dominant factor influencing hydrogen entry under the investigated conditions.
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.