Synthesis of Ni@Al2O3 nanocomposite with superior activity and stability for hydrogen production from plastic-derived syngas by CO2-sorption-enhanced reforming

被引:10
作者
Wu, Shan-Luo [1 ]
Wey, Ming-Yen [1 ]
机构
[1] Natl Chung Hsing Univ, Dept Environm Engn, Taichung 402, Taiwan
关键词
Hydrogen production; Core-shell catalyst; Functional materials; CO2; reforming; CATALYTIC AIR GASIFICATION; CORE-SHELL CATALYST; WASTE POLYPROPYLENE; LOW-TEMPERATURE; FLUIDIZED-BED; ACETIC-ACID; STEAM; NI; METHANE; DRY;
D O I
10.1016/j.ijhydene.2021.09.246
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
Catalytic dry (CO2) reforming of plastic-derived syngas is a promising method of producing hydrogen-rich syngas and reducing greenhouse gases. The development of catalysts with high activity and stability is critical for this reaction. In this study, we fabricated core-shell structured Ni@Al2O3 catalysts with different shell thicknesses using advanced polyol and sol-gel methods. The effects of different Al/Ni ratios on the activity and stability of the catalysts in the CO2 reforming reaction were investigated. The main challenge for CO2 reforming of methane is carbon deposition. In the developed catalysts, the mesoporous Al2O3 coating outside the Ni core enhances the stability. However, the interaction between the core and the shell strongly affects the catalyst activity and product selectivity in the reaction. The catalyst with an Al/Ni ratio of 2 exhibited the highest methane conversion of up to 88% and the lowest carbon deposition, compared to the congeners with Al/Ni ratios of 1 and 3. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:39728 / 39735
页数:8
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