Molecular dynamics simulation of CO2 permeation and separation in Zr-MOF membranes

Abstract

Global warming due to greenhouse gas emissions has continuously threatened the climate and environment. Zirconium-based metal-organic frameworks (Zr-MOFs) with Zr6 inner cores represent a subfamily of nanoporous materials with good physicochemical stabilities, showing significant prospects for practical applications in gas separation. A molecular simulation study is reported here to investigate the membrane separation of CO2/N2 and CO2/CH4 mixtures in five Zr-MOFs (Zr-fum, UiO-66, DUT-52, Zr-cca, UiO-67) with similar ligand in their structures and different pore-limiting diameter (PLD) ranging from 0.36 nm to 0.59 nm. The gas permeation and separation performance are evaluated with the concentration gradient-driven molecular dynamics (CGD-MD) method. The results show that the separation of both gas mixtures is dominated by the preferential sorption of CO2 over N2 and CH4, respectively. Meanwhile, the PLD of MOFs is also a significant factor governing permeation. MOFs with a larger PLD have a higher permeability and a lower selectivity for CO2/N2 and CO2/CH4 separation. Free-energy profiles were calculated to describe the insights into CO2 separation, that the larger PLD can cause a lower energy barrier when gases transport through the pore of MOFs. The results were compared with the grand canonical Monte Carlo and equilibrium molecular dynamics (GCMC + EMD) approach, a traditional method to predict gas adsorption and diffusion in MOFs. As the GCMC+EMD approach neglected the interaction between components and potential mass transfer resistance at the surface of the membranes, the results obtained from the CGD-MD method in this work are more reliable. This study provides microscopic insights into CO2 separation in Zr-MOF membranes and suggests their potential use for gas separation.