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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.
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页码:677 / 687
页数:11
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