The catalytic cracking of 1-methylnaphthalene individually and in bina
ry combination with n-hexadecane on zeolite catalysts is reported. It
is shown that for cracking of the polyaromatic feed over HY zeolite, t
he major processes are isomerisation and disproportionation. In the bi
nary mixture, product selectivity is unchanged when compared to cracki
ng of the individual components. The relative reactivity of the linear
alkane in the presence of the alkyldiaromatic is significantly reduce
d, and may be attributed to blockage of either zeolite pores or acid s
ites on the zeolite surface. For cracking of the binary mixture over a
combination of HY and HZSM-5 zeolites, shifts in product selectivity
when compared to those for cracking over the faujasite catalyst alone,
suggest that the pentasil additive acts to suppress bimolecular hydro
gen transfer processes on HY zeolite.