Summary As the largest carbon-emitting region in China, the feasibility of basalt geological carbon sequestration in the Yangtze River Basin is an important way to address regional carbon neutrality. In this study, we carried out carbonation reactions in a closed experimental setup using synthetic formation water to test the basalt-CO2 interaction by using the alkaline olivine basalt from the Yangtze River Basin of China. We used scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), and inductively coupled plasma mass spectrometry (ICP-MS) to characterize the solid and liquid phases before and after the reaction and to obtain the carbonation degree. Comparing the mineral characteristics with those of the unreacted samples, the results consistently show a reduction in silicate minerals and an increase in carbonate minerals, regardless of reaction conditions or time. The experimental results show that the CO2 consumption rate during the carbon sequestration process of basalt in the Yangtze River Basin has a characteristic time threshold, and after 180 days of reaction, the rate tends to stabilize under all reaction conditions. In addition, the percentage of CO2 consumed under high-pressure conditions was significantly greater than under low-pressure conditions. Considering the limitations of traditional potential calculation methods, we propose a new calculation method for predicting the CO2 sequestration potential of basalt based on the analysis and summary of changes in mineral content after the reaction. According to this calculation, the potential total CO2 reserves of Cenozoic and Mesozoic alkaline basalt distributed in southeastern China are estimated to be 2.117 billion tons of CO2, approximately equivalent to China’s carbon emissions for 2 years, providing support for the feasibility of basalt carbon sequestration in China. While these findings support the potential of basalt carbon sequestration in the region, further research is needed to validate these estimates under field conditions, considering the differences in reactive surface area between powdered and in-situ basalts.
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