High quality H2-rich syngas production from pyrolysis-gasification of biomass and plastic wastes by Ni-Fe@Nanofibers/Porous carbon catalyst

被引:92
|
作者
Zhang, Shuping [1 ,2 ]
Zhu, Shuguang [1 ]
Zhang, Houlei [1 ]
Liu, Xinzhi [1 ]
Xiong, Yuanquan [2 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Energy & Power Engn, Nanjing 210094, Jiangsu, Peoples R China
[2] Southeast Univ, Sch Energy & Environm, Key Lab Energy Thermal Convers & Control, Minist Educ, Nanjing 210096, Jiangsu, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Syngas; Pyrolysis-gasification; Biomass; Plastic; Carbon-based catalyst; ONE-POT SYNTHESIS; RICE HUSK; HYDROGEN-PRODUCTION; CO-GASIFICATION; TAR; CHAR; PERFORMANCE; COMPOSITES; CONVERSION; HYDROCHAR;
D O I
10.1016/j.ijhydene.2019.08.105
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
To produce the high quality H-2-rich syngas from biomass and plastic wastes, a two-stage pyrolysis-gasification system involving pyrolysis and catalytic gasification is considered as a suitable route. Generally, synthesis of highly active, low cost and coke-resistant catalyst for tar cracking is the key factor. A series of monometallic catalysts of Ni@CNF/PCs and Fe@CNF/PCs and the bimetallic Ni-Fe@CNF/PCs catalyst were prepared by a simple one-step pyrolysis approach for high quality syngas production from pyrolysis-gasification of biomass and plastic wastes. The results indicated that the bimetallic Ni-Fe@CNF/PCs catalyst appeared as the optimal catalyst in affording the best compromise between catalytic activity and stability with the existence of the excellent dispersibility of the Fe0.64Ni0.36 alloy nanoparticles and the carbon nanofibers/porous carbon composite structure. In addition, the optimal operation conditions of biomass/plastic ratio of 1/2 and gasification temperature of 700 degrees C were observed for the bimetallic Ni-Fe@CNF/PCs catalyst to play best roles in the H-2-rich syngas quality, with up to 33.66 mmol H-2/g biomass, and tar yields as low as 5.66 mg/g. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:26193 / 26203
页数:11
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