Competitive adsorption mechanisms of multicomponent gases in kaolinite under electric fields: A molecular perspective

Abstract

The investigation of the competitive adsorption mechanisms of gas mixtures within the inorganic nanopores of shale influenced by an electric field holds paramount importance for improving shale gas recovery and enhancing CO2 storage efficiency. This study employs molecular dynamics (MD) simulations to investigate the competitive adsorption mechanisms of gas mixtures on kaolinite surfaces. Subsequently, the engineering parameters governing electric field-enhanced CO2 sequestration and enhanced gas recovery (CS-EGR) are explored and optimized. In the absence of an electric field, the analysis reveals that water molecules exhibit the highest adsorption capacity in a ternary H2O–CO2–CH4 mixture, resulting in the formation of a water film of a specific thickness. CO2 displays a superior adsorption capability over CH4. As the CO2 volume injected into the reservoir increases, CH4 undergoes desorption due to the dominant adsorption effect of CO2. However, the efficiency of CO2 displacing CH4 diminishes significantly. The introduction of an electric field alters the equilibrium state of the gas mixture, leading to a further increase in CO2 adsorption and enhancing its selectivity relative to that of CH4 by 33%. These findings lay the foundation for the practical implementation of electric field-enhanced CS-EGR in shale reservoirs.