The adsorption of ammonia, pyridine and benzene on non-dealuminated (S
i/Al=4.4) and dealuminated (Si/Al= 10 and 30) mazzite samples was foll
owed by FT-IR spectroscopy. The dealumination of mazzites (by steaming
and acid treatment) made all their narrow channels accessible to pyri
dine. Pyridine and ammonia adsorption and desorption showed that the b
road OH band at approximately 3600 cm(-1) was composed of several subm
axima corresponding to hydroxyl groups of various localizations and va
rious acid strengths. With all the mazzite samples, the concentrations
of Bronsted acid sites determined by ammonia adsorption were comparab
le with the values calculated from the chemical composition of zeolite
s (amounts of Al minus amount of Na) whereas those determined from pyr
idine adsorption were lower than these values. The greatest difference
was found for the non-dealuminated MAZ-4.4, in which pyridine could n
ot reach the sites of the narrow channels. The values of the extinctio
n coefficients corresponding to the OH groups located in the large cha
nnels were higher than those corresponding to the OH groups of the nar
row channels, thus showing the stronger acidity of the former OH group
s. The acid strength of OH groups increased with the dealumination, as
seen from the increase in the corresponding extinction coefficient an
d frequency shift Delta v due to the hydrogen bonding of hydroxyl grou
ps with benzene. Furthermore, the protonic acidity of the dealuminated
mazzite of Si/Al= 30 was found to be stronger than that of mordenite
and beta zeolite with comparable Si/Al. (C) 1998 Elsevier Science B.V.