The catalytic activity of superacidic catalysts on the basis of SO4/Zr
O2 in n-alkane isomerization is studied. Such systems are shown to rev
eal high activity in the isomerization of paraffins, and their catalyt
ic properties depend on the length of the carbon chain in the alkane a
nd on the nature of the modifying additives. Isomerization of n-butane
proceeds via a bimolecular mechanism on strong Bronsted acid sites. I
ntroduction of gallium enhances the catalytic activity of SO4/ZrO2 in
the isomerization of rt-butane due to stabilizaton of acidic centers a
nd the ability of gallium to activate alkane molecules. Isomerization
of n-hexane proceeds essentially via a monomolecular mechanism involvi
ng dehydrogenation of the paraffin as an intermediate step. Introducti
on of platinum increases the catalytic activity of the SO4/ZrO2 system
in n-hexane isomerization due to enhancement of dehydrogenating prope
rties of the catalyst.