Sustainable Synthesis of a Highly Stable and Coke-Free Ni@CeO2 Catalyst for the Efficient Carbon Dioxide Reforming of Methane

被引:11
|
作者
Kim, Seung Bo [1 ]
Eissa, Ahmed Al-Shahat [1 ,2 ]
Kim, Min-Jae [1 ]
Goda, Emad S. [3 ]
Youn, Jae-Rang [1 ]
Lee, Kyubock [1 ]
机构
[1] Chungnam Natl Univ, Grad Sch Energy Sci & Technol, 99 Daehak Ro, Daejeon 34134, South Korea
[2] South Valley Univ, Sch Sci, Dept Chem, Qena 83523, Egypt
[3] Hannam Univ, Dept Chem, Organ Nanomat Lab, Daejeon 34054, South Korea
关键词
dry reforming of methane; coke resistance; durability; deactivation; syngas; SYNGAS PRODUCTION; ACTIVE-SITES; CERIA; NICKEL; OXIDATION; SURFACE; CEO2; NANOPARTICLES; INSIGHT; NI/CEO2;
D O I
10.3390/catal12040423
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
A facile and green synthetic strategy is developed in this paper for the construction of an efficient catalyst for the industrially important carbon dioxide reforming of methane, which is also named the dry reforming of methane (DRM). Through controlling the synthetic strategy and Ni content, a high-performance Ni@CeO2 catalyst was successfully fabricated. The catalyst showed superb efficiency for producing the syngas with high and stable conversions at prolonged operating conditions. Incorporating Ni during the ceria (CeO2) crystallization resulted in a more stable structure and smaller nanoparticle (NP) size with a more robust interaction with the support than loading Ni on CeO2 supports by the conventional impregnation method. The H-2/CO ratio was almost 1.0, indicating the promising applicability of utilizing the obtained syngas for the Fischer-Tropsch process to produce worthy chemicals. No carbon deposits were observed over the as-synthesized catalyst after operating the DRM reaction for 50.0 h, even at a more coke-favoring temperature (700 degrees C). Owing to the superb resistance to coke and sintering, control of the size of the Ni-NPs, uniform dispersion of the active phase, and potent metal interaction with the support, the synthesized catalyst achieved a magnificent catalytic activity and durability during serving for the DRM reaction for extended operating periods.
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页数:22
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