催化作用
甲醇
甲烷
化学
甲烷转化炉
合成气
蒸汽重整
无机化学
化学工程
等离子体
核化学
催化重整
二氧化碳重整
制氢
非热等离子体
材料科学
工业催化剂
一氧化碳
二氧化碳
作者
Nabil Majd Alawi,Ho Hong Quyen,Hoang M. Nguyen,Jamal Manee Ali,Ouf A. Shams
标识
DOI:10.1134/s0965544126120078
摘要
Abstract Non-thermal plasma (NTP) enables non-equilibrium activation of CH4 and CO2 under mild conditions, offering an alternative route for low-temperature gas-to-liquid conversion. In this work, methane bi-reforming (CH4/H2O/CO2 = 3 : 2 : 1) to methanol was investigated over Cu-based catalysts in a dielectric barrier discharge (DBD) reactor under three configurations: thermal catalysis (no plasma), in-plasma catalysis (IPC), and post-plasma catalysis (PPC). Experiments were conducted at atmospheric pressure with discharge power ranging from 30 to 60 W, corresponding to a specific energy input (SEI) of 15‒30 J/cm3. Discharge power was quantified using the Lissajous method. Among the tested configurations, IPC exhibited the best performance, achieving CH4 and CO2 conversions of 35 and 30%, respectively, a space-time yield of 3.6 mmol g–1 h–1, and an energy efficiency of 5.5% at SEI ≈ 22 J/cm3. In contrast, IPC showed higher conversion but lower stability and MeOH selectivity relative to PPC due to direct plasma-catalyst interaction. These results demonstrate that spatial separation of plasma and catalyst effectively enhances methanol selectivity and stability, providing design guidance for compact and decentralized plasma-assisted GTL processes.
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