CO storage in organic nanopores with varying widths: Molecular simulation and simplified local density model.

Accurately characterizing CO adsorption behavior in organic nanopores is a prerequisite for estimating CO storage capacity in shale reservoirs with complex pore structures. This study employs grand canonical Monte Carlo (GCMC) molecular simulations to investigate the CO adsorption characteristics in organic nanopores with varying widths over a wide range of temperatures and pressures. Based on GCMC simulations, the pore width in the simplified Local-Density (SLD) adsorption model is related to key adsorption parameters, enabling the SLD model to evaluate CO storage density rapidly and accurately in organic nanopores under complex reservoir conditions. The research findings suggest that the features of CO excess adsorption curves are mainly influenced by temperature and the number of adsorption layers. Higher temperatures and increased adsorption layers result in higher pressure requirements to achieve the CO excess adsorption peak. Under high pressures, the number of adsorption layers plays a critical role in enhancing the adsorption capacity. Due to the constraints of pore size, there are fewer adsorption layers in micropores, leading to higher CO excess adsorption in mesopores than in micropores under high pressures. In the SLD model, the key parameter Λ decays exponentially with the increase of pore width. The average density of CO in the nanopores calculated by the modified SLD model is in good agreement with the simulation results. Finally, the research reveals that smaller organic nanopore widths result in higher CO densities, with limited sensitivity to temperature and pressure variations. Low pressure and high temperature reservoir conditions are unfavorable for CO storage, but adsorption significantly enhances CO storage density in nanopores, particularly in micropores.