Catalytic reforming of biomass pyrolysis tar using the low-cost steel slag as catalyst

被引:49
作者
Guo, Feiqiang [1 ,2 ,3 ]
Liang, Shuang [1 ,2 ]
Zhao, Xingmin [1 ,2 ]
Jia, Xiaopeng [1 ,2 ]
Peng, Kuangye [1 ,2 ]
Jiang, Xiaochen [1 ,2 ]
Qian, Lin [1 ,2 ]
机构
[1] China Univ Min & Technol, Jiangsu Prov Engn Lab High Efficient Energy Stora, Xuzhou 221116, Jiangsu, Peoples R China
[2] China Univ Min & Technol, Sch Elect & Power Engn, Xuzhou 221116, Jiangsu, Peoples R China
[3] Univ Minnesota, Ctr Biorefining, Bioprod & Biosyst Engn Dept, St Paul, MN 55108 USA
基金
中国国家自然科学基金;
关键词
Biomass; Steel slag; Tar removal; Catalytic reforming; WOODY BIOMASS; STEAM; CRACKING; CHAR; WASTE; DECOMPOSITION; NANOPARTICLES; GASIFICATION; TOLUENE;
D O I
10.1016/j.energy.2019.116161
中图分类号
O414.1 [热力学];
学科分类号
摘要
In this work, the possibility of steel slag as an effective and low-cost catalyst for the decomposition of biomass pyrolysis tar has been explored based on the high content of iron oxides for sustainable syngas production from biomass. By simple calcination treatment at 800 degrees C, the loose structure of the steel slag was formed with the main chemical composition of Fe2O3 and MgFe2O4. The steel slag exhibited good catalytic activity on the cracking of biomass pyrolysis tar, and even higher tar conversion efficiency can be obtained by reusing the steel slag, leading to the increase in syngas yield. The presence of additional steam can further promote the tar reforming reactions, leading to the significant increase in H-2 and CO. At 800 degrees C, the tar conversion efficiency reached 94.1% with a high gas yield of 493.5 mL/g. The interaction between steel slag and reductive gases resulted in the reduction of iron oxides into Fe3O4, and more pores were formed for the spent steel slag, which can enhance the contact between active sites and reactants. These characteristics indicate that steel slag has the potential to be used as an efficient catalyst with excellent stability in the long-term biomass tar removal applications. (C) 2019 Elsevier Ltd. All rights reserved.
引用
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页数:8
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