Improvement of low temperature activity and stability of Ni catalysts with addition of Pt for hydrogen production via steam reforming of ethylene glycol

被引:23
|
作者
Zhao, Xingling [1 ]
Wu, Kai [1 ]
Liao, Weiping [1 ]
Wang, Yingxiong [2 ]
Hou, Xiaoning [2 ]
Jin, Mingshan [1 ]
Suo, Zhanghuai [1 ]
Ge, Hui [2 ]
机构
[1] Yantai Univ, Inst Appl Catalysis, 30 Qingquan Rd, Yantai 264005, Shangdong, Peoples R China
[2] Chinese Acad Sci, Inst Coal Chem, State Key Lab Coal Convers, Taiyuan 030001, Shanxi, Peoples R China
关键词
Ethylene glycol; Steam reforming; Pt-Ni bimetallic catalyst; Hydrogen production; Synergistic effect; NI/SIO2; CATALYST; PTNI-CATALYSTS; ETHANOL; GLYCEROL; METHANE; WATER; CERIA; ZIRCONIA; NICKEL; COBALT;
D O I
10.1016/j.gee.2018.11.002
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
Hydrogen production by steam reforming of ethylene glycol (EG) at 300 degrees C was investigated over SiO2 and CeO2 supported Pt-Ni bimetallic catalysts prepared by incipient wetness impregnation methods. It was observed that impregnation sequence of Pt and Ni can affect the performance of catalysts apparently. Catalyst with Pt first and then Ni addition showed higher EG conversion and H-2 yield owing to the Ni enrichment on the surface and the proper interaction between Pt and Ni. It was observed that although SiO2 supported catalysts exhibited better activity and H-2 selectivity, CeO2 supported ones had better stability. This is attributed to the less coke formation on CeO2. Increasing Pt/Ni ratio enhanced the reaction activity, and Pt-3-Ni-7 catalysts with 3 wt% Pt and 7 wt% Ni showed the highest activity and stability. Ni surficial enrichment facilitated the C-C bond rupture and water gas shift reactions; and Pt addition inhibited methanation reaction. Electron transfer and hydrogen spillover from Pt to Ni suppressed carbon deposition. These combined effects lead to the excellent performance of Pt-3-Ni-7 supported catalysts. (C) 2019, Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V.
引用
收藏
页码:300 / 310
页数:11
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