Selective oxidation of CH4 to CH3OH through plasma catalysis: Insights from catalyst characterization and chemical kinetics modelling

被引:54
|
作者
Yi, Yanhui [1 ,2 ]
Li, Shangkun [1 ,2 ]
Cui, Zhaolun [2 ]
Hao, Yingzi [1 ]
Zhang, Yang [3 ]
Wang, Li [4 ]
Liu, Pei [5 ]
Tu, Xin [6 ]
Xu, Xianming [7 ]
Guo, Hongchen [1 ]
Bogaerts, Annemie [2 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Univ Antwerp, Dept Chem, Res Grp PLASMANT, Univ Pl 1, BE-2610 Antwerp, Belgium
[3] Zhengzhou Univ, Ctr Adv Anal & Gene Sequencing, Sch Mat Sci & Engn, Zhengzhou 450001, Peoples R China
[4] Dalian Maritime Univ, Coll Environm Sci & Engn, Dalian 116026, Liaoning, Peoples R China
[5] Shanghai Jiao Tong Univ, In Situ Ctr Phys Sci, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
[6] Univ Liverpool, Dept Elect Engn & Elect, Liverpool L69 3GJ, Merseyside, England
[7] China Natl Petr Corp, Daqing Chem Res Ctr, Daqing 163714, Peoples R China
基金
中国国家自然科学基金;
关键词
Methane conversion; Plasma catalysis; Selective oxidation; Methanol synthesis; Plasma chemistry; ELECTRON-IMPACT DISSOCIATION; ATMOSPHERIC-PRESSURE; METHANE CONVERSION; ROOM-TEMPERATURE; EXCHANGED ZEOLITES; CO METHANATION; OXYGEN; HYDROGENATION; GAMMA-AL2O3; ACTIVATION;
D O I
10.1016/j.apcatb.2021.120384
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The selective oxidation of methane to methanol (SOMTM) by molecular oxygen is a holy grail in catalytic chemistry and remains a challenge in chemical industry. We perform SOMTM in a CH4/O2 plasma, at low temperature and atmospheric pressure, promoted by Ni-based catalysts, reaching 81 % liquid oxygenates selectivity and 50 % CH3OH selectivity, with an excellent catalytic stability. Chemical kinetics modelling shows that CH3OH in the plasma is mainly produced through radical reactions, i.e., CH4 + O(1D) -> CH3O + H, followed by CH3O + H + M -> CH3OH + M and CH3O + HCO -> CH3OH + CO. The catalyst characterization shows that the improved production of CH3OH is attributed to abundant chemisorbed oxygen species, originating from highly dispersed NiO phase with strong oxide support interaction with gamma-Al2O3, which are capable of promoting CH3OH formation through E-R reactions and activating H2O molecules to facilitate CH3OH desorption.
引用
收藏
页数:11
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