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Silica material variation for the MnxOy-Na2WO4/SiO2

MPG-Autoren
http://pubman.mpdl.mpg.de/cone/persons/resource/persons21557

Girgsdies,  Frank
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Manuscript-26.05.pdf
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Zitation

Yildiz, M., Aksu, Y., Simon, U., Otremba, T., Kailasam, K., Göbel, C., et al. (2016). Silica material variation for the MnxOy-Na2WO4/SiO2. Applied Surface Science, 525, 168-179. doi:10.1016/j.apcata.2016.06.034.


Zitierlink: http://hdl.handle.net/11858/00-001M-0000-002B-18D9-3
Zusammenfassung
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 appli-cation, showing a high methane conversion and C2 selectivity, with a good stability during long-termcatalytic activity tests. In the present study, some results have been already published and discussedbriefly in our previous short communication. However, we herein investigated comprehensively theinfluence of various silica support materials on the performance of the MnxOy-Na2WO4/SiO2 systemin the OCM by means of ex situ and in situ XRD, BET, SEM and TEM characterization methods andshowed 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 substan-tially. However, the performance of the SBA-15 supported catalyst was outstanding and the methaneconversion was nearly twofold higher in comparison to the other silica supported catalysts at similar C2 selectivity as shown before in the communication. The reason of this substantial increase in performancecould be the ordered mesoporous structure of the SBA-15 support material, homogeneous dispersion ofactive components and high number of active sites responsible for the OCM.