Iron nanoparticles in situ encapsulated in biochar-based carbon as an effective catalyst for the conversion of biomass-derived syngas to liquid hydrocarbons

被引:168
|
作者
Yan, Qiangu [1 ]
Wan, Caixia [1 ]
Liu, Jian [2 ]
Gao, Jinsen [2 ]
Yu, Fei [1 ]
Zhang, Jilei [3 ]
Cai, Zhiyong [4 ]
机构
[1] Mississippi State Univ, Dept Agr & Biol Engn, Mississippi State, MS 39762 USA
[2] China Univ Petr, State Key Lab Heavy Oil, Beijing 102249, Peoples R China
[3] Mississippi State Univ, Dept Forest Prod, Mississippi State, MS 39762 USA
[4] US Forest Serv, USDA, Forest Prod Lab, Madison, WI USA
基金
美国国家科学基金会;
关键词
FISCHER-TROPSCH SYNTHESIS; X-RAY-DIFFRACTION; MOSSBAUER-SPECTROSCOPY; ACTIVATION; PYROLYSIS; CHEMISTRY; SUPPORT; SPHERES; METAL;
D O I
10.1039/c3gc37107g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biochar, a by-product from the fast pyrolysis of pine wood, was used as the support material for the synthesis of carbon-encapsulated iron nanoparticles. The nanoparticles were characterized for physicochemical properties by multiple morphological and structural methods (e. g., SEM, TEM, XRD, FTIR, and TPD). The Fischer-Tropsch synthesis (FTS) process was carried out to evaluate the catalytic activity of the nanoparticles on conversion of biomass-derived synthesis gas (bio-syngas) to liquid hydrocarbons. Characterization results revealed that the nanoparticles had core-shell structures with iron in situ encapsulated within a graphitic shell. Moreover, significant amounts of iron carbide (mainly Fe3C) were formed as an interface between the carbonaceous shell and the iron core. FTS tests indicated that such carbon-encapsulated iron nanoparticles possessed a high activity on conversion of bio-syngas and good selectivity towards liquid hydrocarbons (of which olefins were the dominant product). Over a 1500 h testing period, the nanoparticles showed striking stability against deactivation, with CO conversion maintained at about 95% and liquid hydrocarbon selectivity at about 68%.
引用
收藏
页码:1631 / 1640
页数:10
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