Plasma-catalytic reforming of CO₂-rich biogas over Ni/γ-Al₂O₃ catalysts in a rotating gliding arc reactor

Zhu, Fengsen, Zhang, Hao, Yan, Xin, Yan, Jianhua, Ni, Mingjiang, Li, Xiaodong and Tu, Xin ORCID: 0000-0002-6376-0897 (2017) Plasma-catalytic reforming of CO₂-rich biogas over Ni/γ-Al₂O₃ catalysts in a rotating gliding arc reactor. FUEL, 199. pp. 430-437.

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Abstract

The combination of plasma and heterogeneous catalysis has been considered as an attractive and promising process for the synthesis of fuels and chemicals. In this work, plasma-catalytic reforming of biogas is carried out over Ni/γ-Al2O3 catalysts with different Ni loadings (6 wt.%, 8 wt.% and 10 wt.% Ni) in a novel rotating gliding arc (RGA) plasma reactor. In the plasma reforming of biogas without a catalyst, the CH4 conversion can reach up to 52.6% at a CH4/CO2 molar ratio of 3:7 and a total flow rate of 6 L/min. The combination of the RGA with the Ni/γ-Al2O3 catalysts enhances the performance of the plasma biogas reforming: increasing Ni loading enhances the conversion of CH4 and the maximum CH4 conversion of 58.5% is achieved when placing the 10 wt.% Ni/γ-Al2O3 catalyst in the downstream of the RGA reactor. The presence of the 10 wt.% Ni/γ-Al2O3 catalyst in the RGA reactor also increases the H2 yield by 17.6% compared to the reaction in the absence of a catalyst. A comparison of biogas reforming using different plasma technologies shows that the RGA plasma provides a higher conversion, significantly enhanced processing capacity and reduced energy cost for biogas conversion and syngas production. In addition, compared to biogas reforming using other non-thermal plasmas (e.g. dielectric barrier discharge), the RGA reforming process produces much cleaner gas products in which syngas is the major one.

Item Type:	Article
Uncontrolled Keywords:	Rotating gliding arc (RGA), Plasma-catalysis, Biogas reforming, Syngas
Depositing User:	Symplectic Admin
Date Deposited:	07 Apr 2017 14:14
Last Modified:	12 Oct 2023 11:05
DOI:	10.1016/j.fuel.2017.02.082
Related URLs:	Author Publisher
URI:	https://livrepository.liverpool.ac.uk/id/eprint/3006864