Opposite effects of self-growth amorphous carbon and carbon nanotubes on the reforming of toluene with Ni/α-Al2O3 for hydrogen production

被引:63
作者
He, Limo [1 ]
Hu, Song [1 ,2 ]
Jiang, Long [1 ]
Syed-Hassan, Syed Shatir A. [1 ,3 ]
Wang, Yi [1 ]
Xu, Kai [1 ]
Su, Sheng [1 ,2 ]
Xiang, Jun [1 ,2 ]
Xiao, Lingfeng [1 ]
Chi, Huanying [2 ]
Chen, Xiaofang [2 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Energy & Power Engn, 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
[3] Univ Teknol MARA, Fac Chem Engn, Shah Alam 40450, Selangor, Malaysia
基金
中国国家自然科学基金;
关键词
Hydrogen-rich gas; Ni catalyst; Catalytic activity; Steam reforming; Amorphous carbon; Carbon nanotubes; TAR MODEL-COMPOUND; CHEMICAL-VAPOR-DEPOSITION; NI-BASED CATALYSTS; BIOMASS GASIFICATION; RAMAN-SPECTROSCOPY; NICKEL-CATALYSTS; STEAM; MECHANISM; PYROLYSIS; ACETYLENE;
D O I
10.1016/j.ijhydene.2017.04.230
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
Ni-based catalysts are prone to be deactivated by carbon deposition. This study aims to investigate the influence mechanism of different types of carbon deposition on the activity of Ni/alpha-Al2O3 catalyst at various steam-to-carbon (S/C) ratios during steam reforming of toluene for hydrogen production. At a low S/C ratio of 1, the catalytic activity of Ni/alpha-Al2O3 was inhibited due to the covering and blocking of Ni active sites by the formation of amorphous carbon on the Ni surface. While at a high S/C ratio of 3, more than 80 wt% of carbon deposition was found to be self-growth carbon nanotubes (CNTs) with an average diameter of around 15 nm. The activity of Ni/alpha-Al2O3 in steam reforming of toluene was unusually promoted, which can be attributed to the tip-growth mechanism of CNTs, whereby the Ni particles migrated to the tip or the surface of CNTs, resulting in the improved active site dispersion. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:14439 / 14448
页数:10
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