Influence of Surface Groups on the Diffusion of Gases in MCM-41: A Molecular Dynamics Study

Jennifer J. Williams, Nigel A. Seaton, Tina Duren

Research output: Contribution to journalArticlepeer-review

Abstract

The diffusion of binary mixtures of CO2 and N-2 in a series of functionalized MCM-41 materials was studied using molecular dynamics (MD) simulations. Transport diffusion coefficients were obtained in order to assess the effect of surface functionalization with organic groups. Unmodified MCM-41 was found to be transport selective for N-2. The spatial distribution of the two coadsorbed species showed that N-2 molecules permeated faster and occupied the central pore region to a greater extent than CO2 molecules. CO2 was found to have a much lower permeability than N-2 due to stronger interactions with the surface of MCM-41 and a tendency to become trapped in nooks in the amorphous pore wall. This effect was not reproduced when using a more simplistic model pore with a smooth surface demonstrating the importance of using a realistic pore model. Larger aminophenyl surface groups were found to significantly reduce the N-2 selectivity due to a decrease in the flux of N-2 and an increase in the flux of CO2. We explain this effect in terms of the marked difference in the transport mechanisms of CO2 and N-2 in functionalized MCM-41 materials. Lastly, we remark on the importance of calculating the cross-term diffusion coefficients for this series of materials.

Original languageEnglish
Pages (from-to)10651-10660
Number of pages10
JournalJournal of Physical Chemistry C
Volume115
Issue number21
DOIs
Publication statusPublished - 2 Jun 2011

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