Based on a comparison between simulated and measured adsorption properties,
we demonstrate that both normal and monomethylparaffins are able to fully
enter the pores of TON-, MTT-, and AEL-type molecular sieves. This disprove
s the theory that monomethylparaffins only partially enter these pores and
that normal paraffins are predominantly hydroisomerized at the pore mouths
of these sieves. Instead, we attribute the high selectivity for paraffins w
ith terminal methyl groups to product shape selectivity, and the low select
ivity for paraffins with neighboring methyl groups to transition state sele
ctivity. These traditional shape selectivity concepts explain not only the
detailed product distribution of n-heptane hydroconversion, but also that o
f longer-chain n-paraffins. (C) 1999 Academic Press.