Molecular Simulation of CO(2) and H(2) Encapsulation in a Nanoscale Porous Liquid

In this study we analyse from a theoretical perspective the encapsulation of both gaseous H [Formula: see text] and CO [Formula: see text] at different conditions of pressure and temperature in a Type II porous liquid, composed by nanometric scale cryptophane-111 molecules dispersed in dichloromethane, using atomistic molecular dynamics. Gaseous H [Formula: see text] tends to occupy cryptophane–111’s cavities in the early stages of the simulation; however, a remarkably greater selectivity of CO [Formula: see text] adsorption can be seen in the course of the simulation. Calculations were performed at ambient conditions first, and then varying temperature and pressure, obtaining some insight about the different adsorption found in each case. An evaluation of the host molecule cavities accessible volume was also performed, based on the guest that occupies the pore. Finally, a discussion between the different intermolecular host–guest interactions is presented, justifying the different selectivity obtained in the molecular simulation calculations. From the results obtained, the feasibility of a renewable separation and storage method for CO [Formula: see text] using these nanometric scale porous liquids is pointed out.