Co-activation of methane and nitrogen to acetonitrile over MoCx/Al2O3 catalysts

Korawich Trangwachirachai, I. Ting Kao, Wei Hsiang Huang, Chi Liang Chen, Yu Chuan Lin

研究成果: Article同行評審

摘要

Methane and nitrogen are regarded as the most abundant sources of hydrocarbons and nitrogen, respectively. Both compounds exhibit high stability due to the presence of daunting C-H and N = N bond energies of 439 and 945 kJ mol−1, respectively, leading to their abundance. This study investigates the co-activation of methane and nitrogen using Al2O3-supported MoCx catalysts (1, 5, and 10 wt%) to produce acetonitrile (ACN) at ambient pressure. It was found that the optimum methane conversion (26.1%) and turnover frequency (TOF) of ACN (15.3 h−1) were achieved at 750 °C using 1 wt% Mo loading. To alleviate catalyst deactivation resulting from coking, H2 co-feeding was implemented and found to effectively sustain the on-stream activity for 50 hours. A plausible mechanism for ACN production, which occurs on the MoC-like surface, was proposed.

原文English
頁(從 - 到)5248-5258
頁數11
期刊Catalysis Science and Technology
13
發行號18
DOIs
出版狀態Published - 2023 8月 4

All Science Journal Classification (ASJC) codes

  • 催化

指紋

深入研究「Co-activation of methane and nitrogen to acetonitrile over MoCx/Al2O3 catalysts」主題。共同形成了獨特的指紋。

引用此