Unraveling Diffusion and Other Shape Selectivity Effects in ZSM5 Using n-Hexane Hydroconversion Single-Event Microkinetics

Potentially dominant factors governing the shape selectivity in n-hexane hydroconversion over a Pt/H-ZSM5 catalyst were evaluated by means of single-event microkinetic (SEMK) model regression against experimental data. The observed product distribution could be adequately modeled, and a corresponding physically meaningful interpretation could be made only when accounting for intracrystalline diffusion limitations for each hexane isomer involved in the reaction network, rather than considering physisorption effects or transition-state shape selectivity. Simultaneous diffusion and reaction inside the catalyst crystallites were expressed via Ficks second law, while the alkane Fick diffusion coefficients were assessed by explicitly accounting for mixture nonideality effects. A 3-fold lower diffusion coefficient was found to be required for 3-methylpentane compared with 2-methylpentane to explain the typically high selectivity toward the latter alkane. Once formed inside the catalyst crystallite, dimethylbutane isomers remained nearly immobile as was evident from their significantly lower diffusion coefficients. Reaction at the crystallite external surface was primarily responsible for the marginal conversion toward the former species, as observed experimentally.