Methane dehydroaromatization by Mo/HZSM-5: mono- or bifunctional catalysis?

N. Kosinov, F.J.A.G. Coumans, E. Uslamin, A.S.G. Wijpkema, B. Mezari, E.J.M. Hensen

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Abstract

The active site requirements for methane dehydroaromatization by Mo/HZSM-5 were investigated by employing as catalysts physical mixtures of Mo-bearing supports (HZSM-5, SiO 2, γ-Al 2O 3, and activated carbon) and HZSM-5. Separation of the two catalyst components after activation or reaction was possible by using two different sieve fractions. Our comparison demonstrates that migration of volatile Mo oxides into the micropores of HZSM-5 is at the origin of the observed catalytic synergy in methane dehydroaromatization for physical mixtures. The propensity of Mo migration depends on the activation method and the Mo-support interaction. Migration is most pronounced for Mo/SiO 2. Prolonged exposure of HZSM-5 zeolite to Mo oxide vapors results in partial destruction of the zeolite framework. Mo carbide dispersed on nonzeolitic supports afforded predominantly coke with only very small amounts of benzene. The main function of the zeolite is to provide a shape-selective environment for the conversion of methane to benzene. A comparison of Mo/HZSM-5 and Mo/Silicalite-1 demonstrates that aromatization of methane is an intrinsic ability of molybdenum carbides dispersed in the 10-membered-ring micropores of MFI zeolite. Thus, one important role of the Brønsted acid sites is to promote the dispersion of the Mo oxide precursor and, accordingly, the active Mo carbide phase in the micropores of HZSM-5. (Figure Presented).

Original languageEnglish
Pages (from-to)520–529
Number of pages10
JournalACS Catalysis
Volume7
Issue number1
DOIs
Publication statusPublished - Jan 2017

Keywords

  • Mo/ZSM-5
  • aromatization
  • bifunctional mechanism
  • methane
  • shape selectivity

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