Series
of HY sorbents with different amounts and strength of Brønsted
and Lewis acidic sites were prepared. Their adsorption performance
in thiophene–benzene solution, pure benzene, and pure thiophene
were evaluated, and the desulfurization mechanisms were studied. The
results show that both thiophene and benzene could be effectively
adsorbed through the interaction between Lewis acid sites and the
conjugated π bond in these two molecules, and thus thiophene
adsorption could be obviously competed by benzene on Lewis acidic
sites. By contrast, on Brønsted acidic sites, thiophene can be
efficiently adsorbed via H–S bond, which is stronger than the
former interaction. Moreover, the middle strong Brønsted acid
could cause thiophene oligomerization. Hence, for the desulfurization
purpose by NaY zeolite in aromatic free system, its weak and middle
strong Lewis acid should be increased, and for that in aromatic existing
system, the Brønsted acid site with relative low strength should
be promoted.