Geochemical and physical alteration of clay-rich shales under supercritical CO2 conditions

The injection of Carbon Dioxide (CO2) into shale gas formations is a promising approach that not only reduces the impact of greenhouse gas on climate change but also enhances the gas recovery due to geochemical interactions between CO2 and clay minerals. However, these geochemical interactions have not been fully explored and changes in the petrophysical properties of shales have been reported over time. This paper evaluates the geochemical reactions and physical changes caused by the injection of supercritical carbon dioxide (ScCO2) on the properties of clay-rich shales. Samples from the Eagle Ford formation were collected and exposed to ScCO2 at different pressures ranging from 10 to 24 MPa at 70 degrees C. Analytical methods such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and thin-section microscopy were used to characterize the ScCO2- treated samples. The results showed dissolution of clays and precipitation of quartz with increasing ScCO2 treatment pressure. The content of carbonate minerals was also reduced at high pressure, which can be attributed to the reactions of the dolomite with H+ to form magnesium carbonate. The percentage of absorption of aromatic hydrocarbons and oxygenated groups gradually increased with increasing pressure, which can be attributed to the increase in CO2 adsorption. On the other hand, the absorption of aliphatic and hydroxyl groups decreased after treatment. ScCO2 treatment pressure is an important factor to evaluate the CO2 adsorption capacity of clay rich shales. The presented results enrich the understanding of the interactions between CO2 and shale under different pressures, which may be helpful to determine the feasibility of long-term injection and storage in shale.

Automated summary

This study evaluates the impact of injecting supercritical carbon dioxide into clay-rich shales. Results indicate precipitation of quartz, reduction of carbonate minerals, increased absorption of aromatic hydrocarbons and oxygenated groups, and decreased absorption of aliphatic and hydroxyl groups with increasing pressure.