Hydrogen production from steam reforming of simulated bio-oil over Ce-Ni/Co catalyst with in continuous CO2 capture

被引:43
|
作者
Xie, Huaqing [1 ]
Yu, Qingbo [1 ]
Wei, Mengqi [1 ]
Duan, Wenjun [1 ]
Yao, Xin [1 ]
Qin, Qin [1 ]
Zuo, Zongliang [1 ]
机构
[1] Northeastern Univ, Sch Met & Mat, Shenyang 110819, Liaoning, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
Hydrogen production; Bio-oil; Model compounds; Ni catalyst; CO2; capture; SOLID 2-PHASE MIXTURE; THERMODYNAMIC ANALYSIS; AQUEOUS FRACTION; MODEL COMPOUNDS; FAST-PYROLYSIS; HEAT-TRANSFER; BIOMASS; GLYCEROL; COMPONENTS; NICKEL;
D O I
10.1016/j.ijhydene.2014.11.137
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
For microsized CaO calcinated from calcium acetate as CO2 sorbent, the CO2 adsorption efficiency increased with the increased of temperature, but decreased when the temperature was over 750 degrees C, due to the endothermic decomposition of CaCO3. The decreased CO2 partial pressure was unfavourable to CO2 adsorption. The steam reforming of the simulated bio-oil over the Ce Ni/Co catalyst supported on Al2O3 balls was performed, and the optimal results for hydrogen production were obtained at 700 degrees C, the S/C ratio of 9 and the LsHSV of 0.23 h(-1), with the actual hydrogen yield of 83.8% and the H-2(+CO + CH4) yield of 94.1%. In the steam reforming experiment with in continuous situ CO2 capture, the feeding of CaO into the reforming reactor made the hydrogen concentration improved excellently upto 93.3%. However, the H-2 yield decreased at higher CaO/C ratio, mainly because the excessive CaO restrained the contact between the reactants and the catalyst. Besides, the higher S/C ratio decreasing the CO2 partial pressure, was against the simultaneous CO2 adsorption, with the optimal S/C ratio of 9. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:1420 / 1428
页数:9
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