Sorption enhanced aqueous phase reforming of biodiesel byproduct glycerol for hydrogen production over Cu-Ni bimetallic catalysts supported on gelatinous MgO

被引:11
作者
Liu, Dashuai [1 ]
Dou, Binlin [1 ]
Zhang, Hua [1 ]
Wu, Kai [1 ]
Luo, Chuanqi [1 ]
Du, Jinbo [1 ]
Gao, Dao Xing [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 P, Shanghai 200093, Peoples R China
[2] Chinese Acad Sci, Inst Engn Thermophys, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Hydrogen production; Gelatinous MgO; Cu-Ni; MgO catalyst; Aqueous phase reforming of biodiesel; byproduct glycerol; In -situ CO 2 removal; WATER-GAS SHIFT; H-2; PRODUCTION; ACETIC-ACID; PHENOL; CEO2;
D O I
10.1016/j.jclepro.2022.135491
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Hydrogen production from sorption enhanced aqueous phase reforming (APR) of biodiesel byproduct glycerol was studied by Ni-based monometallic and bimetallic catalysts supported on gelatinous MgO supports. Compared with Ni-based monometallic catalyst, the H2 selectivity and glycerol conversion of the Cu-Ni bimetallic catalyst were found to be increased more than 3% and 30%, respectively. Meanwhile, higher reaction temperature was found to have higher H2 yield with lower H2 selectivity. The H2 yield using the catalyst with gelatinous MgO support was 1.25 times higher than that of calcined support. Through in-situ CO2 capture, the addition of CaO to the Cu-Ni bimetallic catalyst increased more than 58.3% and 14.4% of the H2 yield and selectivity, respectively. An analysis about liquid product component indicate that the presence of CaO promote the further cleavage of the C-C bond, which further increased the conversion of glycerol. Furthermore, it was found that the presence of CaO could also improve the stability of the catalyst through the control experiments.
引用
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页数:12
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