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Cu-Mo2C/MCM-41: An Efficient Catalyst for the Selective Synthesis of Methanol from CO2
被引:41
作者:

Liu, Xiaoran
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机构: Heilongjiang Univ, Coll Heilongjiang Prov, Key Lab Chem Engn Proc & Technol High Efficiency, Int Joint Res Ctr Catalyt Technol, Harbin 150080, Peoples R China

Song, Yingquan
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机构: Heilongjiang Univ, Coll Heilongjiang Prov, Key Lab Chem Engn Proc & Technol High Efficiency, Int Joint Res Ctr Catalyt Technol, Harbin 150080, Peoples R China

Geng, Wenhao
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机构: Heilongjiang Univ, Coll Heilongjiang Prov, Key Lab Chem Engn Proc & Technol High Efficiency, Int Joint Res Ctr Catalyt Technol, Harbin 150080, Peoples R China

Li, Henan
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机构: Heilongjiang Univ, Coll Heilongjiang Prov, Key Lab Chem Engn Proc & Technol High Efficiency, Int Joint Res Ctr Catalyt Technol, Harbin 150080, Peoples R China

Xiao, Linfei
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机构: Heilongjiang Univ, Coll Heilongjiang Prov, Key Lab Chem Engn Proc & Technol High Efficiency, Int Joint Res Ctr Catalyt Technol, Harbin 150080, Peoples R China

Wu, Wei
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机构:
Heilongjiang Univ, Coll Heilongjiang Prov, Key Lab Chem Engn Proc & Technol High Efficiency, Int Joint Res Ctr Catalyt Technol, Harbin 150080, Peoples R China Heilongjiang Univ, Coll Heilongjiang Prov, Key Lab Chem Engn Proc & Technol High Efficiency, Int Joint Res Ctr Catalyt Technol, Harbin 150080, Peoples R China
机构:
[1] Heilongjiang Univ, Coll Heilongjiang Prov, Key Lab Chem Engn Proc & Technol High Efficiency, Int Joint Res Ctr Catalyt Technol, Harbin 150080, Peoples R China
来源:
关键词:
CO2;
hydrogenation;
Cu-promoted Mo2C;
supported catalyst;
methanol synthesis;
MOLYBDENUM CARBIDES;
CARBON-DIOXIDE;
METAL-OXIDE;
HYDROGENATION;
ACTIVATION;
CONVERSION;
ZNO;
CU;
VALORIZATION;
PERFORMANCE;
D O I:
10.3390/catal6050075
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:
Supported molybdenum carbide (yMo(2)C/M41) and Cu-promoted molybdenum carbide, using a mechanical mixing and co-impregnation method (xCuyMo(2)C/M41-Mand xCuyMo(2)C/M41-I) on a mesoporous molecular sieve MCM-41, were prepared by temperature-programmed carburization method in a CO/H-2 atmosphere at 1073 K, and their catalytic performances were tested for CO2 hydrogenation to form methanol. Both catalysts, which were promoted by Cu, exhibited higher catalytic activity. In comparison to 20Cu20Mo(2)C/M41-M, the 20Cu20Mo(2)C/M41-I catalyst exhibited a stronger synergistic effect between Cu and Mo2C on the catalyst surface, which resulted in a higher selectivity for methanol in the CO2 hydrogenation reaction. Under the optimal reaction conditions, the highest selectivity (63%) for methanol was obtained at a CO2 conversion of 8.8% over the 20Cu20Mo(2)C/M41-I catalyst.
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