F. Collignon et al., Liquid phase synthesis of MTBE from methanol and isobutene over acid zeolites and amberlyst-15, J CATALYSIS, 182(2), 1999, pp. 302-312
The liquid phase synthesis of methyl tert-butyl ether (MTBE) from methanol
and isobutene over II-Beta and US-Y zeolite catalysts was studied in the te
mperature range 30-120 degrees C. Up to 100 degrees C, commercial II-Beta z
eolite samples with small crystal size were more active than acid Amberlyst
-15 (reference catalyst) and noticeably more active than US-Y, confirming r
esults obtained under vapour phase conditions. The influence of methanol/is
obutene (MeOH/IB) molar ratio, pressure, and space time on the conversion a
nd MTBE selectivity was investigated. At optimized reaction conditions, MTB
E yields of 85-90% can be reached with zeolite Ii-Beta as well as Amberlyst
-15. On zeolites, side reactions of isobutene are more important than on Am
berlyst-15, necessitating operation at MeOH/IB ratios higher than 1:1. For
the same reason, at high conversion on Ii-Beta, the MTBE yields are more se
nsitive to contact time compared to Amberlyst-15. On II-Beta zeolite, no de
activation was observed during a period of more than 50 h on stream at 65 d
egrees C, 1.4 MPa pressure, and a WHSV of 14 h(-1). The catalytic activity
of the zeolites is related to the external specific surface area, and to th
e concentration of bridging hydroxyls and silanol groups in the mesopores.
A zeolite H-Beta sample with a Si/Al ratio of 36 has an optimum silanol and
bridging hydroxyl content leading to stoichiometric methanol and isobutene
adsorption, highest activity and MTBE yields. (C) 1999 Academic Press.