Comment on "efficient Conversion of Methane to Aromatics by Coupling Methylation Reaction"

Review (2017)
Author(s)

Nikolay Kosinov (Eindhoven University of Technology)

Alexander Parastaev (Eindhoven University of Technology)

Alexandra S.G. Wijpkema (Eindhoven University of Technology)

Ina Vollmer (TU Delft - ChemE/Catalysis Engineering)

J. Gascon (TU Delft - ChemE/Catalysis Engineering)

Freek Kapteijn (TU Delft - ChemE/Catalysis Engineering)

E. J.M. Hensen (Eindhoven University of Technology)

ChemE/Catalysis Engineering
DOI related publication
https://doi.org/10.1021/acscatal.7b00665
More Info
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Publication Year
2017
Language
English
ChemE/Catalysis Engineering
Issue number
7
Volume number
7
Pages (from-to)
4485-4487

Abstract

Liu et al. recently reported their results on coconversion of methane and methanol at 973 K over a typical methane dehydroaromatization (MDA) catalysts, Mo/HZSM-5.1 In this work, the authors claimed that adding a small amount of methanol to a methane feed led to more than two times higher methane conversion, substantially higher xylene and toluene selectivities (i.e., combined ca. 80%, nearly an order of magnitude increase as compared to experiments without methanol), and improved catalyst stability to such an extent that no deactivation was observed during 60 h on stream. If reproducible, this result would be a significant achievement, because formation of coke in the MDA reaction has been considered inevitable hitherto. To support their experimental data, Liu et al. carried out a thermodynamic analysis, whose results were in good agreement with their experimental findings.

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