Several catalysts based on natural bentonite-type clay were synthesize
d, and their physicochemical and catalytic properties in the reaction
of benzene alkylation with olefins were investigated. By pillaring ben
tonite with an oligomeric aluminum-containing hydroxycation, a thermal
ly stable catalyst with a basal spacing of approximately 18 angstrom a
nd a specific surface area of 236 m2/g was prepared. The pillared bent
onite and uncalcined, Al-exchanged clay exhibited high activity in the
reaction of benzene alkylation with high olefins; the conversion Of C
6 - C-12 olefins at 150 - 200-degrees-C reached 100% at a selectivity
to monoalkylbenzenes greater than 80%. When using these olefins, the p
illared clay had no advantages as compared with Al-exchanged bentonite
. The differences were revealed for benzene alkylation with high olefi
ns (hexadecene).