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Sandwich-type Co core@shell nanocomposite (SiO2 @Co@CeO2): Coke resistant catalyst toward CO2 reforming with ethanol
被引:6
作者:

Li, Feifei
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机构:
Dalian Polytech Univ, Fac Light Ind & Chem Engn, Dalian 116023, Peoples R China Dalian Polytech Univ, Fac Light Ind & Chem Engn, Dalian 116023, Peoples R China

Wang, Mingyue
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Dalian Polytech Univ, Fac Light Ind & Chem Engn, Dalian 116023, Peoples R China Dalian Polytech Univ, Fac Light Ind & Chem Engn, Dalian 116023, Peoples R China

Zhang, Jinming
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机构:
Dalian Polytech Univ, Fac Light Ind & Chem Engn, Dalian 116023, Peoples R China Dalian Polytech Univ, Fac Light Ind & Chem Engn, Dalian 116023, Peoples R China

Lin, Xingtao
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机构:
Beijing Univ Technol, Fac Environm & Life, Beijing 100124, Peoples R China Dalian Polytech Univ, Fac Light Ind & Chem Engn, Dalian 116023, Peoples R China

Wang, Dazhi
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Dalian Polytech Univ, Fac Light Ind & Chem Engn, Dalian 116023, Peoples R China Dalian Polytech Univ, Fac Light Ind & Chem Engn, Dalian 116023, Peoples R China

Cai, Weijie
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h-index: 0
机构:
Dalian Polytech Univ, Fac Light Ind & Chem Engn, Dalian 116023, Peoples R China Dalian Polytech Univ, Fac Light Ind & Chem Engn, Dalian 116023, Peoples R China
机构:
[1] Dalian Polytech Univ, Fac Light Ind & Chem Engn, Dalian 116023, Peoples R China
[2] Beijing Univ Technol, Fac Environm & Life, Beijing 100124, Peoples R China
关键词:
SiO2@Co@CeO2;
Ethanol dry reforming;
Confinement effect;
Syngas;
Coke resistant;
HYDROGEN-PRODUCTION;
FLUIDIZED-BED;
DRY;
METHANE;
PERFORMANCE;
OXIDATION;
SUPPORT;
OXIDE;
NI;
CO/GAMMA-AL2O3;
D O I:
10.1016/j.apcata.2022.118605
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 design of highly efficient catalysts for CO2 reforming with ethanol is of great interest due to the serious coke deposition and the sintering of active metal. In this work, sandwich-type Co core@shell catalyst (SiO2 @Co@CeO2) with Co nanoparticles between SiO2 core and CeO2 shell was synthesized by strong electrostatic adsorption method. Interestingly, SiO2 @Co@CeO2 catalyst exhibited the outstanding activity/stability toward CO2 reforming of ethanol in comparison with Co-SiO2 catalyst. A bi-functional mechanism involving active sites on CeO2 shell was proposed. Indeed, cobalt nanoparticles between SiO2 core and CeO2 shell maintained the high dispersion because of the confinement effect, which supplied a stable Co-ceria interface area where the reaction occurred. In addition, CO2 could readily react with the O vacancies in CeO2 shell to form surface oxygen species and CO, which allowed a continuous cleaning of coke. These positive factors could make it as an attractive candidate for dry reforming process.
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