Dehydroaromatization of methane to benzene occurs over a 2 wt% Mo/ZSM-
5 catalyst at 700 degrees C under non-oxidizing conditions. Following
an initial induction period, during which CH4 reactant reduces the ori
ginal Mo6+ ions in the zeolite to Mo2C and deposition of coke occurs,
a benzene selectivity of similar to 70% at a CH4 conversion of 8-10% c
ould be sustained for more than 16 h. X-ray photoelectron spectroscopy
and X-ray powder diffraction measurements indicate that the reduced M
o is highly dispersed in the channels of the zeolite. Initial activati
on of CH4 reactant occurs on Mo2C sites, leading to the formation of C
2H4 as the primary product. The latter then undergoes subsequent oligo
merization reactions on acidic sites of the zeolite to form aromatic p
roducts.