Methane dehydro-aromatization under nonoxidative conditions over Mo/HZSM-5catalysts: EPR study of the Mo species on/in the HZSM-5 zeolite

EPR characterization of the Mo species on/in the HZSM-5 zeolite is describe d. Four different EPR signals, denoted as signals A, B, D, and E, respectiv ely, have been recorded on the Mo/HZSM-5 sample during its stepwise reducti on by methane. Different Mo species were identified on the basis of their r educibility and the nature of the signal concerned. There are two kinds of Mo species on the Mo/HZSM-5 sample, which are located at different position s on/in the HZSM-5 zeolite. The first kind of the Mo species is polynuclear and located on the external surface. They are either in the octahedral-coo rdinated MoO3 crystallite form (denoted as MoO3 oct) or in the MoOx form wi th a square-pyramidal coordination (denoted as MoO(x)squ). The second kind of the Mo species is associated with the Al atom in the lattice channels of the zeolite. The Mo species associated with Al are mononuclear species, wh ich migrate or diffuse into the channels of the HZSM-5 during calcination. The EPR signals of migrating Mo ion (signals D and E) have hyperfine struct ures which are caused by the interaction between the Mo species and the lat tice Al atom. And the corresponding Mo species are located at two different positions close to the Bronsted Al atoms: AI(I) ... MoOx, and AI(II) ... M oOx. The order of reducibility of these four kinds of species is as follows : MoO(3)oct approximate to MoO(x)squ > AI(I) ... MoOx > AI(II) ... MoOx. It was found that the O-2(-) species might exist on the surface of the Mo/HZS M-5 catalyst during the induction period of the reaction. The variation of the different Mo species in a 6%Mo/HZSM-5 sample during the reaction course is illustrated, and the relationship between the catalytic performance and the intensity of the ESR spectra is discussed. It is proposed that Mo2C is located at the external surface, while partial reduced Mo species associat ed with the Al atom is inside the channel during the reaction. Both of thes e Mo species play a key role in methane dehydro-aromatization. (C) 2000 Aca demic Press.