Abstract

First-order phenomena that may take place in molecular sieve structures besides intracrystalline diffusion shift the effective diffusivity. This shift depends on the ratio of rates of mobilizing and immobilizing the sorbate in the microporous structure. The corresponding uptake curves obtain an unusual but characteristic shape. The phenomenon is exemplified by the system p-xylene/microporous gallosilicate of MFI-type. For the quantification of the kinetic parameters [intracrystalline diffusivities, (im)-mobilization rates], the Volterra integral equation technique is used.

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