Abstract
To elucidate the microscopic mechanisms of competitive adsorption between CO(2) and CH(4) under deep coal seam geological conditions, and to clarify the intrinsic advantages of CO(2) adsorption sequestration and CH(4) displacement from a molecular-scale perspective, this study conducts a systematic investigation using molecular simulation methods. A molecular structure model of coal was constructed and optimized based on elemental analysis and petrographic data of a representative deep coal sample. Combined grand canonical Monte Carlo (GCMC) and molecular dynamics (MD) simulations were employed to systematically analyze the adsorption capacity, density distribution, adsorption heat, adsorption potential energy, and adsorption selectivity of equimolar CO(2)/CH(4) mixtures under geologically constrained conditions of high temperature (308-348 K), high pressure (0-20 MPa), and experimentally measured moisture contents (0-3.58%). The results demonstrate that CO(2) consistently exhibits a significantly stronger competitive adsorption advantage over CH(4) within the coal matrix, with higher adsorption capacity, adsorption heat, and adsorption potential energy and an adsorption selectivity coefficient always greater than 1. Increasing the temperature generally weakens the adsorption capacity of both gases, with CO(2) showing greater sensitivity to temperature variations. At intermediate temperature (328 K) and moderate-to-high pressure, the CO(2) adsorption density exhibits a nonmonotonic trend, reaching a peak, whereas the CH(4) adsorption density decreases monotonically with increasing temperature. Increasing overall moisture content suppresses adsorption behavior; however, at low moisture content (approximately 1.22%), CO(2) adsorption capacity and density are enhanced under high-pressure conditions, creating a favorable microscopic environment for CO(2) retention. With further increases in the moisture content, the saturated adsorption capacity and density of both gases decrease markedly, with a more pronounced decline observed for CO(2). This study reveals, at the molecular scale, the regulatory mechanisms of temperature, pressure, and moisture content on CO(2)-CH(4) competitive adsorption behavior and clarifies the critical role of coal matrix adsorption in geological CO(2) sequestration. The findings provide a theoretical basis for evaluating the potential of CO(2)-enhanced coalbed methane recovery (CO(2)-ECBM) and adsorption-based sequestration in deep coal seams.