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Intrinsic D2/H2 selectivity of NaX Zeolite: Interplay between adsorption and kinetic factors

Kowalczyk, P., Terzyk, A.P., Gauden, P.A., Furmaniak, S., Pantatosaki, E. and Papadopoulos, G.K. (2015) Intrinsic D2/H2 selectivity of NaX Zeolite: Interplay between adsorption and kinetic factors. The Journal of Physical Chemistry C, 119 (27). pp. 15373-15380.

Link to Published Version: http://dx.doi.org/10.1021/acs.jpcc.5b03913
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Abstract

We present the first calculations of intrinsic D2 over H2 (D2/H2) selectivity in well-defined crystalline nanoporous material, namely, NaX zeolite. Feynman path integrals with realistic force field (Kowalczyk, P.; Gauden, P. A.; Terzyk, A. P.; Pantatosaki, E.; Papadopoulos, G. K. J. Chem. Theory Comput. 2013, 9, 2922-2929) are used to calculate zero- and finite-pressure adsorption D2/H2 selectivity on NaX at 77 K. The kinetic selectivity is computed by classical molecular dynamics with Feynman-Hibbs quantum effective potentials. We found that within Henry's law region the intrinsic D2/H2 selectivity of NaX is only ∼1.22-1.31. On the contrary, the theoretical and experimental adsorption D2/H2 selectivities on NaX are 1.49 and 1.6, respectively. A reduction of adsorption selectivity by approximately 13-19% is explained by faster self-diffusion of H2 than D2 molecules in NaX crystal (i.e., normal isotope kinetic effect on self-diffusion). Our results clearly demonstrate the interplay between adsorption and kinetic factors that may have important implications for separation of H2/D2 mixtures using permselective nanoporous membranes.

Item Type: Journal Article
Murdoch Affiliation: School of Veterinary and Life Sciences
Publisher: American Chemical Society
Copyright: © 2015 American Chemical Society.
URI: http://researchrepository.murdoch.edu.au/id/eprint/27811
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