Non-Oxidative Conversion of Methane into Aromatic Hydrocarbons over Mo/ZSM-5 Catalysts
XII European Congress on Catalysis “Catalysis: Balancing the use of fossil and renewable resources” (EuropaCat-XII)
30 Aug - 4 Sep 2015
||EuropaCat XII. Catalysis: Balancing the use of fossil and renewable resources. XII European Congress on Catalysis, Kazan (Russia), 30 August - 4 September, 2015 : Book of Abstracts
Boreskov Institute of Catalysis. Novosibirsk.2015.
2184 c. ISBN 9785906376107.
Sedelnikov a O.
Zaykovski i V.
Institute of Petroleum Chemistry, Tomsk, Russia
Boreskov Institute of Catalysism, Novosibirsk, Russia
Natural and associated petroleum gases are the most important potential sources for
production of valuable petrochemical products including those of organic synthesis. A
development of one-step catalytic process for conversion of methane, the main component of
natural and associated gases, into aromatic compounds is important to solving the problem of
their rational use and environmental protection. Dehydroaromatization of methane is effective
due to the use of catalytically active high silica zeolites modified with transition metal ions.
Regarding that the zeolite H-ZSM-5 containing molybdenum exhibit higher CH4 conversion and
selectivity to benzene than other type’s zeolites. Generally, the catalysts are produced via zeolite
impregnation by metal salt solution or via mechanical mixing of a zeolite with a metal oxide.
The purpose of the present investigation is to examine the influence of different Mo forms and
the method for their introduction into the zeolite matrix on acidic properties, catalytic activity
and stability of Mo/ZSM-5 catalysts in the process of methane dehydroaromatization (DHA)
under non-oxidative conditions. Using high-resolution transmission electron microscopy
(HRTEM) and energy-dispersive X-ray (EDX) spectroscopy, we studied the nature and
distribution of active sites on the surface of Mo/ZSM-5 catalysts.