Methane decomposition by plasma-packed bed non-thermal plasma reactor

[Display omitted] •Non-oxidative methane conversion was achieved by an NTP-DBD model.•Starting from packed-bed DBD plasma-catalysis mode was investigated in detail.•Packed-bed introduced a synergy route through their improved discharge properties.•Catalysts influenced the plasma gas-phase interactio...

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Veröffentlicht in:Chemical engineering science 2022-08, Vol.258, p.117779, Article 117779
Hauptverfasser: Chawdhury, Piu, Bhanudas Rawool, Sarita, Umamaheswara Rao, M., Subrahmanyam, Ch
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Sprache:eng
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Zusammenfassung:[Display omitted] •Non-oxidative methane conversion was achieved by an NTP-DBD model.•Starting from packed-bed DBD plasma-catalysis mode was investigated in detail.•Packed-bed introduced a synergy route through their improved discharge properties.•Catalysts influenced the plasma gas-phase interaction to surface mechanism. A dielectric barrier discharge reactor (DBD) was employed as a non-thermal plasma (NTP) source for non-oxidative conversion of methane at ambient condition. The reactor was later operated as packed-bed DBD and also served with catalyst coupling. In the bed, dielectric materials (glass beads, BaTiO3) as well as some catalytic support materials (TiO2, SiO2 and γ-Al2O3 beads) were introduced in order to find out the non-catalytic reaction mechanism. Typical results indicated that the non-catalytic mode could favorably activate the strong C-H bond to produce H2 and light hydrocarbons without applying any oxidant or thermal energy. Apart from the materials property (shape, size, surface area, dielectric constant) different plasma parameters has a strong influence on the reaction performance. The existence of highest methane conversion and products yield was experimentally observed form the catalyst coupled plasma mode which could be reasonably described by their dominant catalytic surface properties. Moreover, the present reactor model found to be able enough in limiting the solid coke formation on catalyst surface.
ISSN:0009-2509
1873-4405
DOI:10.1016/j.ces.2022.117779