Aqueous phase reforming of biodiesel byproduct glycerol over mesoporous Ni-Cu/CeO2 for renewable hydrogen production

被引:0
|
作者
Wu, Kai [1 ]
Dou, Binlin [1 ]
Zhang, Hua [1 ]
Liu, Dashuai [1 ]
Chen, Haisheng [2 ]
Xu, Yujie [2 ]
机构
[1] Univ Shanghai Sci & Technol, Sch Energy & Power Engn, Shanghai Key Lab Multiphase Flow & Heat Transfer, Shanghai 200093, Peoples R China
[2] Chinese Acad Sci, Inst Engn Thermophys, Beijing 100190, Peoples R China
关键词
Hydrogen production; Aqueous phase reforming of biodiesel byproduct glycerol; Mesoporous Ni-Cu/CeO2 catalyst; In-situ CO2 capture; WATER-GAS SHIFT; OXYGENATED HYDROCARBONS; CATALYTIC-PROPERTIES; NICKEL-CATALYSTS; ACETIC-ACID; CU; TEMPERATURE; PLATINUM; NI/ATTAPULGITE; GENERATION;
D O I
10.1016/j.fuel.2021.122014
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Aqueous phase reforming (APR), regarded as one method for inexpensive H-2 production, was widely studied due to lower temperature and unnecessary to vaporize water and fuels. In this study, the mesoporous CeO2, regarded as a metal oxide carrier, was first prepared by colloidal solution combustion, and then the Ni-Cu bimetallic supported on mesoporous CeO2 was successfully synthesized to investigate the catalytic performance in APR of biodiesel byproduct glycerol. The results show that the Cu element in the catalysts can effectively improve water-gas shift (WGS) reaction and inhibit the formation of methane, which increases the H-2 production rate from 125.08 to 195.57 mu mol.min(-1).g cat(-1). The higher reaction temperature is beneficial to the H-2 production rate, but not to H-2 selectivity. Kinetics analysis indicates that catalyst of 1Ni2Cu/CeO2 + 0.2gCaO has the lowest apparent activation energy (29.86 kJ.mol(-1)). CaO is introduced as an absorbent to improve WGS reaction and reduce methanation reactions through in-situ CO2 removal and capture. The reaction path and mechanism of APR of glycerol are also discussed in this paper.
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页数:12
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