F.E. Furcas , S. Mundra , F. Somaini , O.B. Isgor , U.M. Angst
{"title":"Steel dissolution in carbonate environments","authors":"F.E. Furcas , S. Mundra , F. Somaini , O.B. Isgor , U.M. Angst","doi":"10.1016/j.corsci.2025.112899","DOIUrl":null,"url":null,"abstract":"<div><div>The electrochemical dissolution of carbon steel exposed to aqueous carbonates stands as one of the main causes for the deterioration of carbon capture, utilisation and storage facilities, pipelines, hydrocarbon refining equipment and reinforced concrete structures. To unlock the full potential of carbon capture applications and ensure the structural integrity of existing chemical processing and civil infrastructure, a thorough understanding of the mechanism of steel dissolution is needed. Here, we leverage advancements in thermodynamic modelling calculations to re-evaluate the stability of the <figure><img></figure> -C-H<sub>2</sub>O system. In combination with electrochemical measurements under controlled hydrodynamic conditions, we show that the electrochemical dissolution in the form of the iron carbonate complex <figure><img></figure> is solely controlled by the pH dependent carbonate equilibrium. The resultant kinetic mechanism is in full agreement with the experimentally obtained dissolution rates and the thermodynamic calculations. We envision the here used methodology to be applied to the dissolution of other metals exposed to a broad range of electrolyte compositions.</div></div>","PeriodicalId":290,"journal":{"name":"Corrosion Science","volume":"253 ","pages":"Article 112899"},"PeriodicalIF":7.4000,"publicationDate":"2025-04-24","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/S0010938X25002264","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
Abstract
The electrochemical dissolution of carbon steel exposed to aqueous carbonates stands as one of the main causes for the deterioration of carbon capture, utilisation and storage facilities, pipelines, hydrocarbon refining equipment and reinforced concrete structures. To unlock the full potential of carbon capture applications and ensure the structural integrity of existing chemical processing and civil infrastructure, a thorough understanding of the mechanism of steel dissolution is needed. Here, we leverage advancements in thermodynamic modelling calculations to re-evaluate the stability of the -C-H2O system. In combination with electrochemical measurements under controlled hydrodynamic conditions, we show that the electrochemical dissolution in the form of the iron carbonate complex is solely controlled by the pH dependent carbonate equilibrium. The resultant kinetic mechanism is in full agreement with the experimentally obtained dissolution rates and the thermodynamic calculations. We envision the here used methodology to be applied to the dissolution of other metals exposed to a broad range of electrolyte compositions.
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.