Study on the Interaction Mechanisms among CO<sub>2</sub>, the Formation Water, and Tight Sandy Conglomerate
Tight sandy conglomerate reservoirs exhibit poor physical properties, strong heterogeneity, and significant development challenges due to low permeability. Understanding the interaction of CO<sub>2</sub> with such formations is critical for enhanced oil recovery (EOR). Experimental studies on the interaction mechanisms among CO<sub>2</sub>, formation water, and tight sandy conglomerate were conducted. The results indicate that under the reservoir conditions of 89 °C and 37.0 MPa, the solubility of CO<sub>2</sub> in the formation water is significantly influenced by temperature, pressure, and salinity. After dissolving in formation water, CO<sub>2</sub> forms carbonic acid, which triggers dissolution reactions of minerals such as feldspar under acidic conditions. This leads to a reduction in feldspar mineral content and a 0.31% decrease in core mass. Concurrently, the rock's microscopic surface becomes rougher with numerous dissolution pores and cavities emerging. The average pore-throat radius increases, and the displacement pressure decreases. These alterations improve the rock's pore structure by enlarging pore-throat dimensions, creating additional flow channels for oil and gas migration. Consequently, the permeability increases by 7.4-11.0%, thereby enhancing the production capacity of tight sandy conglomerate reservoirs.
Authors
- Haiming Gao (ORCID: https://orcid.org/0000-0002-1643-4765)
- Kai-gui Liao
- Ge Wu
- Heng Yong
- Wanfen Pu (ORCID: https://orcid.org/0000-0002-7681-1980)
Institutions
- Sinopec (China) (CN)
- Southwest Petroleum University (CN)
- State Key Laboratory of Oil and Gas Reservoir Geology and Exploitation (CN)
- Research Institute of Petroleum Exploration and Development (CN)
Publication Details
- Journal
- ACS Omega
- Published
- 2025-09-12
- DOI
- https://doi.org/10.1021/acsomega.5c05004
- Primary Topic
- CO2 Sequestration and Geologic Interactions
- Type
- article
- Field-Weighted Citation Impact
- 0.00