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Peculiarities of Dehydroaromatization of CH4-C2H 6 and CH4 over Mo/ZSM-5 Catalysts Full article

Journal Reaction Kinetics and Catalysis Letters
ISSN: 0133-1736 , E-ISSN: 1588-2837
Output data Year: 2009, Volume: 98, Number: 1, Pages: 59-67 Pages count : 9 DOI: 10.1007/s11144-009-0080-7
Tags Benzene, Carbonaceous deposit, Ethane dehydroaromatization, Methane, Mo/ZSM-5
Authors Matus Ekaterina V. 1 , Sukhova Olga B. 1 , Ismagilov Ilyas Z. 1 , Tsikoza Lidiya T. 1 , Ismagilov Zinfer R. 1
Affiliations
1 Boreskov Institute of Catalysis, 630090 Novosibirsk, Russia

Funding (1)

1 International Association for the Promotion of Co-operation with Scientists from the New Independent States of the Former Soviet Union 03-55-1568

Abstract: The peculiarities of dehydroaromatization (DHA) of a CH4–C2H6 mixture over 1–10% Mo/ZSM-5 catalysts (Si/Al = 17, 30, 45) were studied in comparison with reactions of individual hydrocarbons. For a (90 vol.% CH4 + 10 vol.% Ar) mixture, the methane conversion passes through a maximum and decreases with the time-on-stream, being about 12% after 6 h. Experiments with a mixture (85 vol.% CH4 + 5 vol.% C2H6 + 10 vol.% Ar) demonstrated that the presence of ethane leads to the suppression of the methane conversion practically to zero and to an increase in the benzene formation rate in comparison with the (CH4 + Ar) mixture. Characterization of the spent Mo/ZSM-5 catalysts by DTA and TGA showed that both the condensation degree of the carbonaceous deposits (C/H ratio) and their content are higher in the presence of ethane. For both feed compositions, the maximal benzene formation rate was observed over the catalyst with 2 wt% Mo and Si/Al = 17. It is proposed that the formation of C2 intermediates from methane and their further transformations in DHA compete with the ethane aromatization, presumably on the same Mo active sites.
Cite: Matus E.V. , Sukhova O.B. , Ismagilov I.Z. , Tsikoza L.T. , Ismagilov Z.R.
Peculiarities of Dehydroaromatization of CH4-C2H 6 and CH4 over Mo/ZSM-5 Catalysts
Reaction Kinetics and Catalysis Letters. 2009. V.98. N1. P.59-67. DOI: 10.1007/s11144-009-0080-7 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Dec 22, 2008
Accepted: Jul 20, 2009
Published online: Sep 2, 2009
Published print: Oct 1, 2009
Identifiers:
Web of science: WOS:000270190100008
Scopus: 2-s2.0-70349524740
Elibrary: 15298970
Chemical Abstracts: 2009:1184527
Chemical Abstracts (print): 153:264445
OpenAlex: W2032384875
Citing:
DB Citing
Web of science 15
Scopus 15
Elibrary 17
OpenAlex 15
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