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Generalized Hydrodynamic Treatment of the Interplay between Restricted Transport and Catalytic Reactions in Nanoporous Materials
Author(s) -
David M. Ackerman,
Jing Wang,
James W. Evans
Publication year - 2012
Publication title -
physical review letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.688
H-Index - 673
eISSN - 1079-7114
pISSN - 0031-9007
DOI - 10.1103/physrevlett.108.228301
Subject(s) - nanoporous , scaling , diffusion , desorption , chemical reaction , thermodynamics , catalysis , adsorption , materials science , tracer , reaction–diffusion system , penetration (warfare) , chemical physics , porous medium , physics , chemistry , porosity , nanotechnology , quantum mechanics , mathematics , biochemistry , geometry , operations research , composite material
Behavior of catalytic reactions in narrow pores is controlled by a delicate interplay between fluctuations in adsorption-desorption at pore openings, restricted diffusion, and reaction. This behavior is captured by a generalized hydrodynamic formulation of appropriate reaction-diffusion equations (RDE). These RDE incorporate an unconventional description of chemical diffusion in mixed-component quasi-single-file systems based on a refined picture of tracer diffusion for finite-length pores. The RDE elucidate the nonexponential decay of the steady-state reactant concentration into the pore and the non-mean-field scaling of the reactant penetration depth.

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