Platinum-tin supported catalysts at various tin and platinum contents
were prepared by the sol-gel method by adding tetrabutyltin to a homog
eneous solution containing aluminum tri-sec-butoxide (TEA). After gela
tion, the solids were dried, calcined and then impregnated with an aqu
eous solution of hexachloroplatinic acid. Catalysts prepared by this m
ethod show specific BET areas around 270 m(2)/g and platinum dispersio
n up to 90%. Ammonia adsorption shows that there are less acidic sites
in tin-alumina sol-gel preparations than in sol-gel alumina. Activity
measurements for n-heptane dehydrocyclization show that Pt-Sn sol-gel
catalysts are more active than catalysts prepared by successive impre
gnation of a commercial alumina. Moreover, selectivity to benzene form
ation was found 54% lower with sol-gel catalysts than with commercial
based catalysts. A high tolerance to thiophene poisoning during n-hept
ane dehydrocyclization was also found. Additional catalytic tests for
cyclohexane dehydrogenation, isopropanol dehydration and toluene dealk
ylation were performed. High selectivity to acetone in the dehydration
reaction and very low activity for toluene dealkylation were found fo
r sol-gel preparations. The high activity in n-heptane dehydrocyclizat
ion and the high selectivity to acetone in Pt-Sn-alumina sol-gel catal
ysts was interpreted as a result of the modification by tin of the sup
port acidity. Nevertheless, the tolerance to thiophene poisoning and t
he low dealkylation rate observed for sol-gel preparations can only be
explained by an important tin-alumina support effect on platinum acti
vity.