{"title":"碳酸盐含盐含水层CO2捕获的反应输运模型:润湿性、温度和盐度对矿化和储存效率的耦合影响","authors":"Reza Khoramian , Miras Issakhov , Peyman Pourafshary , Saule Aidarova , Altynay Sharipova","doi":"10.1016/j.fuel.2025.137038","DOIUrl":null,"url":null,"abstract":"<div><div>Secure long-term storage of carbon dioxide (CO<sub>2</sub>) in saline aquifers requires a clear understanding of how reservoir conditions and geochemical reactions influence rock properties and trapping mechanisms. While the individual effects of wettability, temperature, and salinity have been examined, their combined impact, particularly under varying wettability states where hysteresis controls phase behavior, remains insufficiently quantified. This study employs reactive transport modeling to assess the effects of temperature (50–90 °C), salinity (70,000–210,000 ppm NaCl), and wettability on CO<sub>2</sub> mineralization, dissolution, and capillary trapping in carbonate-rich formations. Geochemical reactions involving calcite, kaolinite, and anorthite are modeled using transition state theory, while water-wet and mixed-wet conditions are represented through relative permeability and capillary pressure curves that capture wettability-dependent flow behavior. Mineralization increases from ∼ 4.4 × 10<sup>6</sup> to ∼ 1.3 × 10<sup>7</sup> mol in mixed-wet systems from 50 °C to 90 °C, while capillary trapping decreases from ∼ 67 % to ∼ 54 % (water-wet) and ∼ 48 % to ∼ 36 % (mixed-wet), and dissolution rises to > 30 %. At 90 °C, increasing salinity shifts CO<sub>2</sub> plumes from vertically elongated, dissolution-dominant (∼36 %) in mixed-wet to laterally confined, capillary-dominant (∼82 %) in water-wet systems, governed by hysteresis (0.2 vs. 0.35). Calcite precipitation declines by ∼ 22 % (water-wet) with temperature and by ∼ 14 % with salinity, while kaolinite precipitation triples and anorthite dissolution varies from − 25 % to + 90 % depending on wettability. Over 60 years, porosity and permeability increase modestly by ∼ 0.36 % and ∼ 1.22 %. These findings clarify how wettability-driven interfacial dynamics influence mineralization and phase trapping, providing mechanistic guidance for optimizing CO<sub>2</sub> storage performance across diverse reservoir settings.</div></div>","PeriodicalId":325,"journal":{"name":"Fuel","volume":"406 ","pages":"Article 137038"},"PeriodicalIF":7.5000,"publicationDate":"2025-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Reactive transport modeling of CO2 trapping in carbonate saline aquifers: Coupled effects of wettability, temperature, and salinity on mineralization and storage efficiency\",\"authors\":\"Reza Khoramian , Miras Issakhov , Peyman Pourafshary , Saule Aidarova , Altynay Sharipova\",\"doi\":\"10.1016/j.fuel.2025.137038\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Secure long-term storage of carbon dioxide (CO<sub>2</sub>) in saline aquifers requires a clear understanding of how reservoir conditions and geochemical reactions influence rock properties and trapping mechanisms. While the individual effects of wettability, temperature, and salinity have been examined, their combined impact, particularly under varying wettability states where hysteresis controls phase behavior, remains insufficiently quantified. This study employs reactive transport modeling to assess the effects of temperature (50–90 °C), salinity (70,000–210,000 ppm NaCl), and wettability on CO<sub>2</sub> mineralization, dissolution, and capillary trapping in carbonate-rich formations. Geochemical reactions involving calcite, kaolinite, and anorthite are modeled using transition state theory, while water-wet and mixed-wet conditions are represented through relative permeability and capillary pressure curves that capture wettability-dependent flow behavior. Mineralization increases from ∼ 4.4 × 10<sup>6</sup> to ∼ 1.3 × 10<sup>7</sup> mol in mixed-wet systems from 50 °C to 90 °C, while capillary trapping decreases from ∼ 67 % to ∼ 54 % (water-wet) and ∼ 48 % to ∼ 36 % (mixed-wet), and dissolution rises to > 30 %. At 90 °C, increasing salinity shifts CO<sub>2</sub> plumes from vertically elongated, dissolution-dominant (∼36 %) in mixed-wet to laterally confined, capillary-dominant (∼82 %) in water-wet systems, governed by hysteresis (0.2 vs. 0.35). Calcite precipitation declines by ∼ 22 % (water-wet) with temperature and by ∼ 14 % with salinity, while kaolinite precipitation triples and anorthite dissolution varies from − 25 % to + 90 % depending on wettability. Over 60 years, porosity and permeability increase modestly by ∼ 0.36 % and ∼ 1.22 %. These findings clarify how wettability-driven interfacial dynamics influence mineralization and phase trapping, providing mechanistic guidance for optimizing CO<sub>2</sub> storage performance across diverse reservoir settings.</div></div>\",\"PeriodicalId\":325,\"journal\":{\"name\":\"Fuel\",\"volume\":\"406 \",\"pages\":\"Article 137038\"},\"PeriodicalIF\":7.5000,\"publicationDate\":\"2025-10-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fuel\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0016236125027632\",\"RegionNum\":1,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ENERGY & FUELS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fuel","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0016236125027632","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
Reactive transport modeling of CO2 trapping in carbonate saline aquifers: Coupled effects of wettability, temperature, and salinity on mineralization and storage efficiency
Secure long-term storage of carbon dioxide (CO2) in saline aquifers requires a clear understanding of how reservoir conditions and geochemical reactions influence rock properties and trapping mechanisms. While the individual effects of wettability, temperature, and salinity have been examined, their combined impact, particularly under varying wettability states where hysteresis controls phase behavior, remains insufficiently quantified. This study employs reactive transport modeling to assess the effects of temperature (50–90 °C), salinity (70,000–210,000 ppm NaCl), and wettability on CO2 mineralization, dissolution, and capillary trapping in carbonate-rich formations. Geochemical reactions involving calcite, kaolinite, and anorthite are modeled using transition state theory, while water-wet and mixed-wet conditions are represented through relative permeability and capillary pressure curves that capture wettability-dependent flow behavior. Mineralization increases from ∼ 4.4 × 106 to ∼ 1.3 × 107 mol in mixed-wet systems from 50 °C to 90 °C, while capillary trapping decreases from ∼ 67 % to ∼ 54 % (water-wet) and ∼ 48 % to ∼ 36 % (mixed-wet), and dissolution rises to > 30 %. At 90 °C, increasing salinity shifts CO2 plumes from vertically elongated, dissolution-dominant (∼36 %) in mixed-wet to laterally confined, capillary-dominant (∼82 %) in water-wet systems, governed by hysteresis (0.2 vs. 0.35). Calcite precipitation declines by ∼ 22 % (water-wet) with temperature and by ∼ 14 % with salinity, while kaolinite precipitation triples and anorthite dissolution varies from − 25 % to + 90 % depending on wettability. Over 60 years, porosity and permeability increase modestly by ∼ 0.36 % and ∼ 1.22 %. These findings clarify how wettability-driven interfacial dynamics influence mineralization and phase trapping, providing mechanistic guidance for optimizing CO2 storage performance across diverse reservoir settings.
期刊介绍:
The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.