Plasma-catalytic one-step steam reforming of methane to methanol: Revealing the catalytic cycle on Cu/mordenite

被引:0
作者
Hao, Yingzi [1 ]
Li, Shangkun [2 ]
Fang, Wei [1 ]
Wang, Ximiao [1 ]
Cui, Zhaolun [3 ]
Bal, Kristof M. [2 ]
Gerrits, Nick [2 ]
Guo, Hongchen [1 ]
Neyts, Erik C. [2 ]
Bogaerts, Annemie [2 ]
Yi, Yanhui [1 ]
机构
[1] Dalian Univ Technol, Frontier Sci Ctr Smart Mat, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Peoples R China
[2] Univ Antwerp, Dept Chem, Res Grp PLASMANT, Antwerp, Belgium
[3] South China Univ Technol, Sch Elect Power Engn, Guangzhou, Peoples R China
基金
中国国家自然科学基金; 欧洲研究理事会;
关键词
anaerobic oxidation; methane conversion; methanol production; plasma catalysis; SELECTIVE ANAEROBIC OXIDATION; DIRECT CONVERSION; ROOM-TEMPERATURE; COPPER; CU; WATER; BIS(MU-OXO)DICOPPER; ACTIVATION; PATHWAYS; CU-ZSM-5;
D O I
10.1002/aic.18582
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Direct CH4 to CH3OH conversion is a long-standing grand challenge in catalysis. We present one-step steam reforming of methane to methanol (OSRMtM) by combining an atmospheric pressure CH4/H2O/Ar plasma with a Cu/Mordenite (Cu/MOR) catalyst at 170 degrees C, achieving 77% CH3OH selectivity with 3.0% CH4 conversion. Catalyst characterization and plasma diagnostics, as well as D2O and H218O-labeled isotope tracer experiments reveal that the excellent reaction performance is attributed to Cu-O active sites confined by MOR zeolite. During plasma-catalytic OSRMtM, both CH4 and H2O are activated in the plasma and dissociated to produce radicals (CH3, OH, and H). These radicals drive the redox process between Cu2+ and Cu+, playing an important role in plasma-catalytic OSRMtM. Although a gradual reduction of Cu2+ to Cu+ leads to slow deactivation, the catalytic performance can be completely recovered through simple calcination, which enables a continuous plasma-catalytic OSRMtM process using a fluidized-bed reactor.
引用
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页数:12
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