The
influence of hollow ZSM-5 catalysts prepared with two different
kinds of alkalis on catalytic performances in methanol to aromatics
was studied. It was found that benzene, toluene, and xylene (BTX)
selectivities of hollow catalysts were higher than the parent ZSM-5
catalyst due to increasing mesopore volumes and acid strength. Meanwhile,
the catalyst prepared by NaOH treatment exhibited higher BTX selectivity
than the catalyst prepared by tetrapropylammonium hydroxide treatment.
The reason was that the concentration of strong acid sites, Brønsted
acid sites, and framework alumina in channel crossings was higher
than that of the catalyst prepared by NaOH treatment. All these favored
the formation of aromatics. Moreover, the introduction of hollow structures
with mesopores improved diffusion behaviors of species and reduced
the deactivation rate of the catalysts. However, a relatively higher
deactivation rate was obtained over the NaOH-treated sample due to
increasing strong acid sites.