甲烷氧化偶联
合成气
甲烷
催化作用
焦炭
甲醇
选择性
化学
部分氧化
甲烷转化炉
无机化学
蒸汽重整
化学工程
材料科学
有机化学
制氢
工程类
作者
Yipei Chen,Xueliang Mu,Xiang Luo,Kaiqi Shi,Gang Yang,Tao Wu
标识
DOI:10.1002/ente.201900750
摘要
The current study reviews the recent development in the direct conversion of methane into syngas, methanol, light olefins, and aromatic compounds. For syngas production, nickel‐based catalysts are considered as a good choice. Methane conversion (84%) is achieved with nearly no coke formation when the 7% Ni‐1%Au/Al 2 O 3 catalyst is used in the steam reforming of methane (SRM), whereas for dry reforming of methane (DRM), a methane conversion of 17.9% and CO 2 conversion of 23.1% are found for 10%Ni/ZrO x MnO x /SiO 2 operated at 500 °C. The progress of direct conversion of methane to methanol is also summarized with an insight into its selectivity and/or conversion, which shows that in liquid‐phase heterogeneous systems, high selectivity (>80%) can be achieved at 50 °C, but the conversion is low. The latest development of non‐oxidative coupling of methane (NOCM) and oxidative coupling of methane (OCM) for the production of olefins is also reviewed. The Mn 2 O 3 –TiO 2 –Na 2 WO 4 /SiO 2 catalyst is reported to show the high C 2 yield (22%) and a high selectivity toward C 2 (62%) during the OCM at 650 °C. For NOCM, 98% selectivity of ethane can be achieved when a tantalum hydride catalyst supported on silica is used. In addition, the Mo‐based catalysts are the most suitable for the preparation of aromatic compounds from methane.
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