M. Rodrigues et al., COKING, AGING AND REGENERATION OF ZEOLITES .18. COKING AND DEACTIVATION OF HZSM-5 AND GA HZSM-5 CATALYSTS DURING PROPENE AROMATIZATION/, Journal de chimie physique et de physico-chimie biologique, 93(2), 1996, pp. 317-330
Coking and deactivation of HZSM-5 (Si/Al = 40) and of a 2 wt% impregna
ted Ga/HZSM-5 catalyst were investigated during propene aromatization
at temperatures between 250 degrees C and 530 degrees C. Whatever the
temperature the rate of propene aromatization is greater on the Ga/HZS
M-5 catalyst than on HZSM-5 while the rates of coking are practically
identical. With both catalysts a minimum is found in the rare of cokin
g for temperatures between 400 and 450 degrees C, which can be explain
ed by a contrary effect of temperature on the race of formation of cok
e precursors and on their retention. Coke causes a pore blockage respo
nsible for the catalyst deactivation, No change in the dehydrogenation
/cracking rate ratio of methylcyclohexane transformation is observed,
which indicates that the dehydrogenating function (Ga species) and the
acid one (protonic sites) are affected to the same extent. The coke c
omposition does not depend on the catalyst but changes very much with
the temperature : alkylmonoaromatics at 250 degrees C, bi- or triaroma
tics at 350 degrees C, tetra- to polyaromatics at 400 and 450 degrees
C, polyaromatics at 530 degrees C. Coke molecules result either from s
uccessive alkylation, cyclization, hydrogen transfer (or dehydrogenati
on) steps or through dehydrogenative coupling of aromatics, the signif
icance of the second mode increasing with the reaction temperature.