Hydrocarbons (C8–C12) separation in porous metallocavitand M-PPX (M = Cu, Ag, Au): From computational insight

Abstract

High throughput computational approach has been employed to investigate the adsorption and separation of C8–C12 hydrocarbons (HCs) on a tube-shaped met allocavitand, pillarplex (PPX). The Cu (I), Ag (I), and Au (I) seamed PPX and their HC complexes has been examined using density functional theory (DFT), pro claiming Cu-PPX has a higher binding affinity with the HCs whereas Ag-PPX is lower. The thermodynamic properties reveal the host–guest complex is stable at ambient condition. Noncovalent interaction (NCI) analysis shows the interaction of guests within the cavity of PPX is mainly attributed by Van der Waals type. The energy decomposition analysis (EDA) enunciates the percentage contribution of dispersion interaction (ΔEdisp) is 59–62%, the electrostatic (ΔEelct) and orbital (ΔEorb) terms have a moderate contribution towards the total binding energy. The Grand canonical Monte Carlo (GCMC) simulation manifests the Cu-PPX and Au PPX are the ideal hosts with the optimum capacity to store HCs at ambient conditions. The octane uptake is 18.01, 17.50, and 25.31 cm3 STP/g in Cu, Ag and Au-PPX and the uptake reduces upon increasing the HC chain length. The isosteric heat of adsorption (Qst) is corroborated with the computed DFT data at ambient setup. The ideal adsorption solution theory (IAST) claims the C8 selectivity in Cu, Ag and Au-PPX is optimum at 298 K and the increasing temperature from 298 K to 323 K, the selectivity of the C9 and C12 in Cu-PPX and Au-PPX, respectively is remarkable after the complete separation of C8. Hence Cu-PPX and Au-PPX is the potential candidate for industrial use to separate the heavy HCs.