费托法
催化作用
化学
热解
碳纤维
选择性
纳米颗粒
化学工程
石墨
壳体(结构)
石墨烯
碳氢化合物
分解
无定形碳
无定形固体
纳米技术
有机化学
材料科学
复合材料
复合数
工程类
作者
Caiping Ma,Wei Zhang,Qiang Chang,Xianzhou Wang,H. Wang,Huimin Chen,Yuxue Wei,Chenghua Zhang,Hongwei Xiang,Yong Yang,Yongwang Li
标识
DOI:10.1016/j.jcat.2020.11.033
摘要
θ-Fe3C formation is usually considered as a deactivation factor in Fischer-Tropsch synthesis (FTS). Herein, θ-Fe3C dominated [email protected] core–shell catalysts were fabricated by pyrolysis of MIL-101(Fe) in ethyne for studying the roles of θ-Fe3C and carbon shell in FTS. In the evolution of MIL-101(Fe) into [email protected] catalysts, ethyne decomposition promotes the formation of θ-Fe3C and carbon shells around nanoparticles. By modulating the pyrolysis temperature, θ-Fe3C and/or α-Fe nanoparticles coated with different carbon shells (amorphous carbon, graphene or graphite shells) are acquired. By exploring the relationship between phase composition, structure of catalysts and FTS performance, it is found that θ-Fe3C is confirmed to be FTS active, which exhibits superior CC chain growth ability, i.e., higher C5+ selectivity and lower CH4 selectivity. Meanwhile, graphene shell inhibits iron nanoparticles aggregation and stabilizes the catalysts.
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