TY - JOUR
T1 - Modeling and assessment of CO2 geological storage in the Eastern Deccan Basalt of India
AU - Liu, Danqing
AU - Agarwal, Ramesh
AU - Liu, Fang
AU - Yang, Sen
AU - Li, Yilian
N1 - Funding Information:
This work was funded by the National Natural Science Foundation of China (Grant No. 41902253) and the Fundamental Research Funds for the Central Universities, China University of Geosciences (Wuhan) (No. CUG192716).
Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
PY - 2022/12
Y1 - 2022/12
N2 - In this study, the CO2 carbonatization potential of the Deccan basalt formation in Eastern India is evaluated by establishing a hydro-chemical field-scale model based on the geological, hydrological, and geochemical parameter of the basalt in the Mandla lobe. The reliable initial mineral thermodynamic parameters are obtained by validating the laboratory scale experiment of CO2-water-basalt reaction with a numerical method. Over 50% of injected carbon mineralized within 140 days for the Deccan basalt in the Mandla lobe, and the majority of CO2 is sequestered as ankerite, siderite, and calcite, which occupy a percent of 65%, 28%, and 7%, respectively. Clay minerals, including smectite and chlorite, are important secondary minerals contributing to the process of CO2 storage in the basaltic reservoir. Clay precipitation can promote the dissolution of silica- and aluminum-rich plagioclase and release Ca2+ to enhance the carbonatization of CO2 to Ca carbonates but competes for Fe2+ and Mg2+ from siderite and magnesite. Clay precipitation also impacts the CO2 carbonatization efficiency by changing the basalt conductivity. CO2 carbonatization efficiency was found to increase with the reduction of injection rate. However, slow flow rate can increase the pore clogging risk and induce large pressure build-up. This is the first field-scale assessment of CO2 mineralization potential of the Deccan basalt, which is one of the largest terrestrial flood basalt formations in the world. The results can provide valuable information and scientific support for India and global carbon mitigation.
AB - In this study, the CO2 carbonatization potential of the Deccan basalt formation in Eastern India is evaluated by establishing a hydro-chemical field-scale model based on the geological, hydrological, and geochemical parameter of the basalt in the Mandla lobe. The reliable initial mineral thermodynamic parameters are obtained by validating the laboratory scale experiment of CO2-water-basalt reaction with a numerical method. Over 50% of injected carbon mineralized within 140 days for the Deccan basalt in the Mandla lobe, and the majority of CO2 is sequestered as ankerite, siderite, and calcite, which occupy a percent of 65%, 28%, and 7%, respectively. Clay minerals, including smectite and chlorite, are important secondary minerals contributing to the process of CO2 storage in the basaltic reservoir. Clay precipitation can promote the dissolution of silica- and aluminum-rich plagioclase and release Ca2+ to enhance the carbonatization of CO2 to Ca carbonates but competes for Fe2+ and Mg2+ from siderite and magnesite. Clay precipitation also impacts the CO2 carbonatization efficiency by changing the basalt conductivity. CO2 carbonatization efficiency was found to increase with the reduction of injection rate. However, slow flow rate can increase the pore clogging risk and induce large pressure build-up. This is the first field-scale assessment of CO2 mineralization potential of the Deccan basalt, which is one of the largest terrestrial flood basalt formations in the world. The results can provide valuable information and scientific support for India and global carbon mitigation.
KW - Aqueous CO
KW - Assessment of GCS
KW - Clays
KW - Deccan basalt
KW - Injection rate
UR - http://www.scopus.com/inward/record.url?scp=85133591635&partnerID=8YFLogxK
U2 - 10.1007/s11356-022-21757-y
DO - 10.1007/s11356-022-21757-y
M3 - Article
C2 - 35799008
AN - SCOPUS:85133591635
SN - 0944-1344
VL - 29
SP - 85465
EP - 85481
JO - Environmental Science and Pollution Research
JF - Environmental Science and Pollution Research
IS - 56
ER -