{"title":"Experimental study on the impact of H2S and H2SO4 in CO2 on five different sealant compositions under conditions relevant for geological CO2-storage","authors":"Reinier van Noort , Gaute Svenningsen , Kai Li","doi":"10.1016/j.geoen.2025.214005","DOIUrl":null,"url":null,"abstract":"<div><div>The integrity of well sealants is a key challenge to secure geological storage of CO<sub>2</sub>. While it has been well-established through experimental research that the exposure of such sealants to CO<sub>2</sub>-bearing fluids can lead to carbonation, and potentially degradation during prolonged exposure or flow, the impact of impurities present in injected CO<sub>2</sub> has not received much consideration.</div><div>This paper reports exposure of five different sealants to simulated well conditions with supercritical CO<sub>2</sub> containing H<sub>2</sub>S or H<sub>2</sub>SO<sub>4</sub> as impurities. Three of these sealants are based on Portland Cement, while the other two are based on Calcium Aluminate Cement, and a rock-based geopolymer specifically developed for Geological CO<sub>2</sub> Storage (GCS). The impact of the impurities on these sealants was assessed through scanning electron microscopy with energy-dispersive X-ray spectroscopy, computed tomography scanning, and fluid chemical analysis, and compared to previous research where the same five sealants were exposed to clean CO<sub>2</sub> under otherwise identical conditions.</div><div>The results show that during exposure to CO<sub>2</sub>-saturated water, the presence of H<sub>2</sub>S mostly resulted in enhanced sealant alteration depths, and reduced carbonate precipitation. During exposure to wet supercritical CO<sub>2</sub>, the presence of H<sub>2</sub>S or H<sub>2</sub>SO<sub>4</sub> resulted in reduced carbonate precipitation, and enhanced alteration depths in some (H<sub>2</sub>S) or all (H<sub>2</sub>SO<sub>4</sub>) sealants. Additionally, relatively minor degradation was observed in the outer 100–200 μm of samples exposed in the presence of H<sub>2</sub>SO<sub>4</sub>. Overall, the impacts of impurities were more pronounced for sealants that were more affected by exposure to clean CO<sub>2</sub>.</div></div>","PeriodicalId":100578,"journal":{"name":"Geoenergy Science and Engineering","volume":"253 ","pages":"Article 214005"},"PeriodicalIF":0.0000,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Geoenergy Science and Engineering","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S294989102500363X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"0","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0
Abstract
The integrity of well sealants is a key challenge to secure geological storage of CO2. While it has been well-established through experimental research that the exposure of such sealants to CO2-bearing fluids can lead to carbonation, and potentially degradation during prolonged exposure or flow, the impact of impurities present in injected CO2 has not received much consideration.
This paper reports exposure of five different sealants to simulated well conditions with supercritical CO2 containing H2S or H2SO4 as impurities. Three of these sealants are based on Portland Cement, while the other two are based on Calcium Aluminate Cement, and a rock-based geopolymer specifically developed for Geological CO2 Storage (GCS). The impact of the impurities on these sealants was assessed through scanning electron microscopy with energy-dispersive X-ray spectroscopy, computed tomography scanning, and fluid chemical analysis, and compared to previous research where the same five sealants were exposed to clean CO2 under otherwise identical conditions.
The results show that during exposure to CO2-saturated water, the presence of H2S mostly resulted in enhanced sealant alteration depths, and reduced carbonate precipitation. During exposure to wet supercritical CO2, the presence of H2S or H2SO4 resulted in reduced carbonate precipitation, and enhanced alteration depths in some (H2S) or all (H2SO4) sealants. Additionally, relatively minor degradation was observed in the outer 100–200 μm of samples exposed in the presence of H2SO4. Overall, the impacts of impurities were more pronounced for sealants that were more affected by exposure to clean CO2.