Zn-modified ZSM-5 catalysts were widely used in ethylene
aromatization;
however, the deactivation and regeneration behavior of these catalysts
have not been fully understood. In this work, the structure evolution
of Zn species on various x-Zn(y)/Z5
catalysts prepared by ion exchange, incipient wetness impregnation,
and physical mixture in ethylene aromatization were systemically investigated.
The results of X-ray diffraction, X-ray photoelectron spectroscopy,
DR UV–vis, 27Al/29Si MAS NMR, EXAFS,
and X-ray absorption near edge spectra with LCF analysis indicated
that the generated coke species on spent Zn/ZSM-5 can not only cover
the acid sites and block the pore channel but also lead to the transformation
of active 6-fold coordinated ZnOH+ species into unactive
4-fold coordinated ZnO. After regeneration to eliminate these carbon
deposits, the crystallinity, specific surface area, pore volume, and
total acid content of regenerated Zn/ZSM-5 were fully recovered. More
importantly, most of the ZnO clusters/crystals were converted into
ZnOH+ species again. As a result, the regenerated Zn/ZSM-5
catalysts showed even higher aromatic selectivity than the fresh one
in ethylene aromatization.