Effects of oxygen species from Fe addition on promoting steam reforming of toluene over Fe-Ni/Al2O3 catalysts

被引:83
作者
Hu, Song [1 ,2 ]
He, Limo [1 ]
Wang, Yi [1 ]
Su, Sheng [1 ,2 ]
Jiang, Long [1 ]
Chen, Qindong [1 ]
Liu, Qicong [2 ]
Chi, Huanying [2 ]
Xiang, Jun [1 ,2 ]
Sun, Lushi [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, State Key Lab Coal Combust, Wuhan 430074, Peoples R China
[2] Huazhong Univ Sci & Technol, China EU Inst Clean & Renewable Energy, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
Steam reforming of toluene; Iron-nickel; Coke deposition; Lattice oxygen; Adsorbed oxygen; BIOMASS GASIFICATION; MODEL-COMPOUND; HYDROGEN-PRODUCTION; LATTICE OXYGEN; TAR; ETHANOL; CONVERSION; GAS;
D O I
10.1016/j.ijhydene.2016.07.271
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
A series of Fe-modified Ni/Al2O3 (FNA) catalysts with different Fe/Ni ratios (Fe/Ni = 0.5, 2, 3) was investigated during steam reforming of toluene as a model compound of biomass tar. The percentages of hydrogen in the product gas reached about 65% over prepared catalysts. The addition of Fe remarkably increased the toluene conversion and reduced the amount of coke. According to X-ray photoelectron spectrometer and pulse injection experiments, the addition of Fe increased the amount of lattice oxygen and adsorbed oxygen on the surface of FNA. The Fe in alloy was easily oxidized to FeOx by steam. The lattice oxygen in FeOx could oxidize the carbon deposited or intermediates on adjacent Ni atoms to produce CO. Meanwhile, the more adsorbed oxygen promoted the further reaction with the intermediates during the steam reforming of toluene. Both the adsorbed oxygen and lattice oxygen from the addition of Fe played important roles in the steam reforming of toluene. For the two types of cokes (amorphous/paraffinic and graphitic/filamentous), the formation of graphitic/filamentous carbon was remarkably suppressed due to the oxidization property of oxygen species from the addition of Fe. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:17967 / 17975
页数:9
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