{"title":"Comparison of Hot Corrosion Behavior of Ni36Fe34Al17Cr10Mo1Ti2 and Ni34Co25Fe12Al15Cr12W2 Alloys in NaCl–KCl–Na2SO4 Salt","authors":"Xiaoming Liu, Fengyang Quan, Yuan Gao, Shaodong Zhang, Jianbin Wang, Zhijun Wang, Junjie Li, Feng He, Jincheng Wang","doi":"10.1007/s40195-024-01791-0","DOIUrl":null,"url":null,"abstract":"<div><p>Hot corrosion in molten salt is a complex process, involving both chemical corrosion and electrochemical corrosion. Interfacial reactions and oxide dissolution can also impact the corrosion results. Compared with single component/type salt, multi-component/type hot corrosion leads to more severe degradation, while the multi-component alloys offer potential chances for developing anti-corrosion metallic materials. In this study, we aim to elucidate the hot corrosion behavior and gain a better understanding of the corrosion mechanism of the multi-component alloys under multi-component/type NaCl-KCl-Na<sub>2</sub>SO<sub>4</sub> salt. The corrosion behavior of dual-phase Ni<sub>36</sub>Fe<sub>34</sub>Al<sub>17</sub>Cr<sub>10</sub>Mo<sub>1</sub>Ti<sub>2</sub> (HEA-1) and Ni<sub>34</sub>Co<sub>25</sub>Fe<sub>12</sub>Al<sub>15</sub>Cr<sub>12</sub>W<sub>2</sub> (HEA-2) alloys was studied within NaCl-KCl-Na<sub>2</sub>SO<sub>4</sub> molten salt with mass ratios of 5:5:1 and 5:5:2. After exposure to the salt at 650 °C for 168 h, it was found that the Ni<sub>34</sub>Co<sub>25</sub>Fe<sub>12</sub>Al<sub>15</sub>Cr<sub>12</sub>W<sub>2</sub> exhibited better corrosion resistance than Ni<sub>36</sub>Fe<sub>34</sub>Al<sub>17</sub>Cr<sub>10</sub>Mo<sub>1</sub>Ti<sub>2</sub>. The improved performance of Ni<sub>30</sub>Co<sub>25</sub>Fe<sub>12</sub>Al<sub>15</sub>Cr<sub>12</sub>W<sub>2</sub> alloy was attributed to the Co element, which facilitated the formation of dense oxides scale and enhanced scale adhesion. Alkali chlorides with stronger penetration ability dominated the corrosion process and alkali sulfate further aggravated the corrosion. The primary corrosion mechanisms involved in this process were identified as “electrochemical mechanism” attacking the body-centered cubic structure in the alloys and “active oxidation” causing dissolution of the alloy elements.</p></div>","PeriodicalId":457,"journal":{"name":"Acta Metallurgica Sinica-English Letters","volume":"38 2","pages":"205 - 217"},"PeriodicalIF":2.9000,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Metallurgica Sinica-English Letters","FirstCategoryId":"1","ListUrlMain":"https://link.springer.com/article/10.1007/s40195-024-01791-0","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"METALLURGY & METALLURGICAL ENGINEERING","Score":null,"Total":0}
引用次数: 0
Abstract
Hot corrosion in molten salt is a complex process, involving both chemical corrosion and electrochemical corrosion. Interfacial reactions and oxide dissolution can also impact the corrosion results. Compared with single component/type salt, multi-component/type hot corrosion leads to more severe degradation, while the multi-component alloys offer potential chances for developing anti-corrosion metallic materials. In this study, we aim to elucidate the hot corrosion behavior and gain a better understanding of the corrosion mechanism of the multi-component alloys under multi-component/type NaCl-KCl-Na2SO4 salt. The corrosion behavior of dual-phase Ni36Fe34Al17Cr10Mo1Ti2 (HEA-1) and Ni34Co25Fe12Al15Cr12W2 (HEA-2) alloys was studied within NaCl-KCl-Na2SO4 molten salt with mass ratios of 5:5:1 and 5:5:2. After exposure to the salt at 650 °C for 168 h, it was found that the Ni34Co25Fe12Al15Cr12W2 exhibited better corrosion resistance than Ni36Fe34Al17Cr10Mo1Ti2. The improved performance of Ni30Co25Fe12Al15Cr12W2 alloy was attributed to the Co element, which facilitated the formation of dense oxides scale and enhanced scale adhesion. Alkali chlorides with stronger penetration ability dominated the corrosion process and alkali sulfate further aggravated the corrosion. The primary corrosion mechanisms involved in this process were identified as “electrochemical mechanism” attacking the body-centered cubic structure in the alloys and “active oxidation” causing dissolution of the alloy elements.
期刊介绍:
This international journal presents compact reports of significant, original and timely research reflecting progress in metallurgy, materials science and engineering, including materials physics, physical metallurgy, and process metallurgy.