Synthesis of modified char-supported Ni-Fe catalyst with hierarchical structure for catalytic cracking of biomass tar

被引:41
作者
Lin, Qunqing [1 ]
Zhang, Shuping [1 ]
Wang, Jiaxing [1 ]
Yin, Haoxin [1 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Energy & Power Engn, Nanjing 210094, 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
Biomass tar; Catalytic cracking; Char-supported Ni-Fe catalyst; Carbon nanofiber; Hierarchical structure; SYNGAS PRODUCTION; RICE HUSK; ACTIVATED CARBON; MODEL-COMPOUND; PYROLYSIS; NANOPARTICLES; PERFORMANCE; CONVERSION; TOLUENE; DECOMPOSITION;
D O I
10.1016/j.renene.2021.04.084
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The ubiquitous challenge of tar problem has limited the further development of biomass pyrolysis/gasification. In view of this, the directional construction of modified char-supported Ni-Fe catalyst by hydrothermal carbonization followed by heat treatment to strengthen tar cracking was reported in this study. At the optimized temperature of 700 degrees C for catalytic cracking, the corresponding tar conversion efficiency of catalyst appeared to be 95.46% with the superior catalytic performance of tar. With the presence of such catalyst, the relative content of polycyclic aromatic hydrocarbon (PAH) compounds in residue tar was drastically reduced due to the high activity of Ni-Fe alloy active phases for the cleavage of tar macromolecules. The hierarchical pore structure derived from the dense carbon nanofiber shell layer and porous carbon core reduced the resistance of tar macromolecules diffusion and promoted the contact with metallic active sites. The Fe atoms enriched on the surface of Ni-Fe alloy with a high oxygen affinity promoted the catalytic cracking reaction of tar. The coated metallic active sites with multi-layer graphitic carbon prevented the catalyst from deactivation and sintering. The results are expected to establish the theory foundation and construction method of char-supported Ni-Fe catalyst for tar catalytic cracking in the industry. (C) 2021 Elsevier Ltd. All rights reserved.
引用
收藏
页码:188 / 198
页数:11
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