Selection of iron-based oxygen carriers for two-step solar thermochemical splitting of carbon dioxide

被引:19
作者
Zhang, Hao [1 ]
Zhang, Xiaomi [1 ]
Yang, Dazhi [1 ]
Shuai, Yong [2 ]
Lougou, Bachirou Guene [2 ]
Pan, Qinghui [2 ]
Wang, Fuqiang [3 ]
机构
[1] Harbin Inst Technol, Sch Elect Engn & Automat, Harbin, Heilongjiang, Peoples R China
[2] Harbin Inst Technol, Sch Energy Sci & Engn, Harbin, Heilongjiang, Peoples R China
[3] Harbin Inst Technol Weihai, Sch Automobile Engn, Weihai, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Solar thermochemistry; Oxygen carrier; Ferrite; CO2; splitting; Reaction kinetics; HYDROGEN-PRODUCTION; SYNGAS PRODUCTION; CO2; CONVERSION; METHANE; FUEL; DISSOCIATION; PERFORMANCE;
D O I
10.1016/j.enconman.2023.116772
中图分类号
O414.1 [热力学];
学科分类号
摘要
The two-step solar thermochemical cycle is a prospective clean energy technology that enables the direct splitting of water and carbon dioxide for solar fuel production. However, immature oxygen carriers fun-damentally restrict the solar-to-fuel conversion efficiency and thus prevent this technology from immediate industrial uptake. Focusing on the conventional iron-based oxygen carriers, this study intends to find a modified oxygen carrier with low reaction temperature requirements and excellent reaction performance, so as to attain dual optimization in terms of thermal efficiency and chemical efficiency. The thermochemical reaction characteristics of six common ferrites and four metal dopants are compared via thermogravimetric analysis under the same programmed temperature control. For further practical applications of the selected oxygen carrier, a foam-structured material with SiC as support is prepared and subsequently experimented in a self -designed 18-kW thermochemical system. The results indicate that the modified oxygen carriers obtained by direct doping of CoFe2O4 with 50wt% NiO exhibit optimal reaction performance, giving the highest CO yield of 439 mu mol/g. Additionally, the foam-structured material enable a peak CO yield of 7.0 mL min-1 g-1 and CO2 conversion of 45.5% at a reduction temperature of only 1100 degrees C, which might be attributed to the micron-scale pore structure as well as the generation of aluminosilicate crystal structures.
引用
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页数:15
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