Plasma-Enhanced Chemical Looping Oxidative Coupling of Methane through Synergy between Metal-Loaded Dielectric Particles and Non-Thermal Plasma

Abstract

A plasma–catalyst hybrid system has been developed for the direct conversion of methane to C2+ hydrocarbons in dielectric barrier discharge (DBD) plasma. TiO2 presented the highest C2+ yield of 11.63% among different dielectric materials when integrated with DBD plasma, which made us concentrate on the TiO2-based catalyst. It was demonstrated that MnTi catalyst showed the best methane coupling performance of 27.29% C2+ yield with 150 V applied voltage, without additional thermal input. The catalytic performance of MnTi catalyst under various operation parameters was further carried out, and different techniques, such as X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, and H2-temperature-programmed reduction were used to explore the effect of Mn loading on methane oxidative coupling (OCM) performance. The results showed that applied voltage and flow rate had a significant effect on methane activation. The dielectric particles of TiO2 loaded with Mn not only synergistically affected the coupling reaction, but also facilitated charge deposition to generate a strong local electric field to activate methane. The synergy effects boosted the OCM performance and the C2+ yield became 1.25 times higher than that of the undoped TiO2 under identical operating conditions in plasma, which was almost impossible to occur even at 850 °C on the MnTi catalyst in the absence of plasma. Moreover, the reaction activity of the catalyst was fully recovered by plasma regeneration at 300 °C and maintained its stability in for at least 30 consecutive cyclic redox tests. This work presents a new opportunity for efficient methane conversion to produce C2+ at low temperatures by plasma assistance.

Keywords

• oxidative coupling of methane
• chemical looping
• synergy effects
• plasma enhancement