Benzene alkylation with propane has been studied on acidic H-MFI zeolites w
ith SiO2/Al2O3 ratios of 51, 104, and 325, mixed (H-MFI + Pt/CeO2) catalyti
c systems, and Pt/H-MFI bifunctional catalysts with Pt content of 0.02 and
0.3%. In some of the experiments, Zr2Fe intermetallic compound was added to
the catalytic system to ensure H-2 removal from the reaction zone. The rea
ction was carried out at atmospheric pressure, in the temperature range of
573-773 K, C3H8/C6H6 = 1, and WHSV = 0.2-7 h(-1). The conversion of propane
and selectivity to propylbenzenes was found to increase in the following o
rder of catalytic systems: H-MFI < (H-MFI + Pt/CeO2) < Pt/H-MFI < (Pt/ H-MF
I + Zr2Fe). The increase of the number of strong Bronsted sites in zeolite
led, on one hand, to the increase of propane conversion, but on the other h
and, to the decrease of the selectivity to target products, which was due t
o the cracking of propane and propylbenzenes dealkylation and dismutation.
Incorporation of Pt into the catalytic system enhanced propane dehydrogenat
ion at the expense of its cracking and resulted in significant improvement
of propane conversion and selectivity to propylbenzenes. Addition of an Hz
scavenger allowed a shift of the thermodynamic equilibria and an increase i
n propane and benzene conversion. The best result was obtained on the (Pt/H
-MFI + Zr2Fe) catalytic system with an SiO2/Al2O3 ratio of 325 and a Pt con
tent of 0.22%, on which the yield of propylbenzenes reached 96% with respec
t to equilibrium and selectivity to propylbenzenes was about 60%. The mecha
nisms of benzene alkylation with propane operating on various catalysts are
discussed. (C) 2000 Academic Press.