Hydrogen production through steam reforming of toluene over Ce, Zr or Fe promoted Ni-Mg-Al hydrotalcite-derived catalysts at low temperature

被引:47
|
作者
Zhou, Fan [1 ]
Pan, Ningyi [1 ]
Chen, Hongyu [1 ]
Xu, Xiang [1 ]
Wang, Chunhao [1 ]
Du, Yankun [1 ]
Guo, Yang [1 ]
Zeng, Zheng [1 ]
Li, Liqing [1 ]
机构
[1] Cent S Univ, Sch Energy Sci & Engn, Changsha 410083, Hunan, Peoples R China
关键词
Catalytic cracking; Hydrotalcite-derived catalysts; Toluene; Carbon deposit; LAYERED DOUBLE HYDROXIDES; TAR MODEL-COMPOUND; CARBON-DIOXIDE; COKE FORMATION; SOLID-WASTE; BIOMASS; METHANE; PYROLYSIS; GASIFICATION; GAS;
D O I
10.1016/j.enconman.2019.06.047
中图分类号
O414.1 [热力学];
学科分类号
摘要
Ni-Mg-Al hydrotalcite-derived materials promoted with Ce, Zr or Fe were prepared by the co-precipitation method, which exhibited excellent performance in steam reforming of toluene (SRT) at low temperature. Especially, Fe-doped catalyst had higher catalytic activity and stability at 400 degrees C, which maintained almost 100% toluene conversion during the SRT reaction (3 h). Moreover, it also had higher hydrogen production and better selectivity for hydrogen production. The physico-chemical characterizations and model simulation indicate its high dispersion of active sites and accessibility of reactants to active sites: uniform dispersion of active sites (SEM, TEM and EDX), large specific surface area (151 m(2)/g), pore volume (0.84 cm(3)/g) and average pore diameter (22.1 nm), small crystallite size (34.9 nm), desirable Ni species reducibility (TPR), high basicity (TPD), low metal carbide formation (XPS), and good adsorption affinity with toluene (- 18.391 kJ mol(-1), DFT). Moreover, less carbon was deposited on the Fe-containing catalyst through measuring the amorphous carbon and CNTs by the TG-MS method, which was due to the tip-growth mechanism of CNTs. Considering lower toluene conversion temperature, higher hydrogen yield, and better resistance to carbon deposition, this study may be meaningful in development of SRT at low temperature.
引用
收藏
页码:677 / 687
页数:11
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