Silica material variation for the MnxOy-Na2WO4/SiO2

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Yildiz M., AKSU Y., Simon U., Otremba T., Kailasam K., Goebel C., ...More

APPLIED CATALYSIS A-GENERAL, vol.525, pp.168-179, 2016 (SCI-Expanded) identifier identifier

  • Publication Type: Article / Article
  • Volume: 525
  • Publication Date: 2016
  • Doi Number: 10.1016/j.apcata.2016.06.034
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.168-179
  • Keywords: Oxidative methane coupling, OCM, MnxOy-Na2WO4/SiO2, Silica support material variation, Mesoporous silica, SBA-15, MEMBRANE REACTOR, STATISTICAL-ANALYSIS, METHANE, CATALYSTS, PERFORMANCE, MN-NA2WO4/SIO2, CONVERSION, MN/NA2WO4/SIO2, ETHYLENE, FUELS
  • Akdeniz University Affiliated: Yes


The oxidative coupling of methane (OCM) is one of the best methods for the direct conversion of methane. Among the known OCM catalysts, MnxOy-Na2WO4/SiO2 is a promising candidate for an industrial application, showing a high methane conversion and C-2 selectivity, with a good stability during long-term catalytic activity tests. In the present study, some results have been already published and discussed briefly in our previous short communication. However, we herein investigated comprehensively the influence of various silica support materials on the performance of the MnxOy-Na2WO4/SiO2 system in the OCM by means of ex situ and in situ XRD, BET, SEM and TEM characterization methods and showed new results to reveal possible support effects on the catalyst. The catalytic performance of most MnxOy-Na2WO4/SiO2 catalysts supported by different silica support materials did not differ substantially. However, the performance of the SBA-15 supported catalyst was outstanding and the methane conversion was nearly twofold higher in comparison to the other silica supported catalysts at similar C-2 selectivity as shown before in the communication. The reason of this substantial increase in performance could be the ordered mesoporous structure of the SBA-15 support material, homogeneous dispersion of active components and high number of active sites responsible for the OCM. (C) 2016 Elsevier B.V. All rights reserved.