Non-Oxidative Coupling of Methane via Plasma-Catalysis Over M/γ-Al2O3 Catalysts (M = Ni, Fe, Rh, Pt and Pd): Impact of Active Metal and Noble Gas Co-Feeding

Plasma-catalysis has attracted significant interest in recent years as an alternative for the direct upgrading of methane into higher-value products. Plasma-catalysis systems can enable the electrification of chemical processes; however, they are highly complex with many previous studies even reporting negative impacts on methane conversion. The present work focuses on the non32 oxidative plasma-catalysis of pure methane in a Dielectric Barrier Discharge (DBD) reactor at atmospheric pressure and with no external heating. A range of transition and noble metals (Ni, Fe, Rh, Pt, Pd) supported on γ-Al2O3 are studied, complemented by plasma-only and support-only experiments. All reactor packings are investigated either with pure methane or co-feeding of helium or argon to assess the role of noble gases in enhancing methane activation via energy transfer mechanisms. Electrical diagnostics and charge characteristics from Lissajous plots, and electron temperature and collision rates calculations via BOLSIG+ are used to support the findings with the aim of elucidating the impact of both active metal and noble gas on the reaction pathways and
activity. The optimal combination of Pd catalyst and Ar co-feeding achieves a substantial
improvement over non-catalytic pure methane results, with C2+ yield rising from 30% to almost 45% at a concurrent reduction of energy cost from 2.4 to 1.7 MJ molCH4−1 and from 9 to 4.7 MJ molC2+−1. Pd, along with Pt, further displayed the lowest coke deposition rates among all packings with overall stable product composition during testing.