Mc. Samolada et al., SELECTIVE O-ALKYLATION OF PHENOL WITH METHANOL OVER SULFATES SUPPORTED ON GAMMA-AL2O3, Journal of catalysis, 152(1), 1995, pp. 52-62
The reaction of phenol with methanol was studied in a fixed-bed reacto
r system as a potential source for the production of methyl aryl ether
s. For this reason, the performance of alumina-supported catalysts imp
regnated with sulphate salts of metals of the groups VIIB and IIB was
studied. The effects of reaction temperature, reaction time, type of m
etal, metal content, and potassium content on the selectivity of methy
l aryl ethers (MAE), as well as the phenol conversion and the yield of
MAE, were established. The reaction temperature and the potassium con
tent were found mainly to affect the selectivity of the catalyst, the
phenol conversion, and the yield of MAE. Empirical equations were deri
ved which proved to be useful for predicting the performance of a cata
lyst over a broad range of reaction conditions. A catalyst (K-3(S)) co
ntaining only potassium (3 wt%) in the form of potassium sulphate supp
orted on gamma-alumina was found to have the most promising performanc
e compared to those reported in the literature in terms of MAE selecti
vity and phenol conversion at atmospheric pressure (selectivity of MAE
= 98%, phenol conversion = 65 wt%). The catalyst remains stable over
a broad range of temperatures (290-330 degrees C). Ks is an inexpensiv
e catalyst, showing major selectivity advantages and product compositi
on (anisole, 92 wt%; o-cresol, 8 wt%) and a low coke production (7 wt%
). The presence of potassium sulphate in the catalyst proved to be the
controlling factor for the production of MAE and it was found to be t
he active phase of the catalyst. The MAE selectivity of potassium sulp
hate catalysts is determined by the potassium content of the catalyst,
while its optimum value is achieved, when acid sites of medium streng
th (+ 1.5 < H-0 less than or equal to + 4.8) with low acidity values (
22 x 10(-4) mmol/m(2)) exist on their surface. (C) 1995 Academic Press
, Inc.