Structural evolution of carbon in an Fe@C catalyst during the Fischer-Tropsch synthesis reaction

被引:27
|
作者
Lyu, Shuai [1 ,2 ,3 ]
Liu, Chengchao [2 ,3 ]
Wang, Guanghui [1 ]
Zhang, Yuhua [2 ,3 ]
Li, Jinlin [2 ,3 ]
Wang, Li [2 ,3 ]
机构
[1] Wuhan Univ Sci & Technol, Sch Chem Engn & Technol, Hubei Key Lab Coal Convers & New Carbon Mat, Wuhan 430081, Hubei, Peoples R China
[2] South Cent Univ Nationalities, Key Lab Catalysis & Mat Sci, State Ethn Affairs Commiss, Wuhan 430074, Peoples R China
[3] South Cent Univ Nationalities, Minist Educ, Wuhan 430074, Peoples R China
关键词
IRON-BASED CATALYSTS; LOWER OLEFINS; CONVERSION; SYNGAS; TRANSFORMATION; HYDROCARBONS; PHASES;
D O I
10.1039/c8cy02420k
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
A pseudo-in situ research method was applied to provide insight into the structural evolution of carbon in an Fe@C catalyst at different stages of the Fischer-Tropsch reaction. Five typical stages of the catalyst were selected for in-depth structural investigation; these were: the fresh catalyst, reduced catalyst, and catalyst in the stable conversion period, in an increased-conversion period and at the inactivation stage. The results indicated that the integral structure of Fe@C constantly changed in the Fischer-Tropsch reaction. Iron carbide transformed from the Fe phase that was easily oxidized under high temperature Fischer-Tropsch conditions, and the carbon framework was completely destroyed in the reaction process, leading to a drastic decrease in the specific surface area of the material. This destruction could have two opposing effects: on the one hand, the loss of carbon could re-expose the active sites that have been covered by carbon at a reaction temperature of 320 degrees C and favor the reaction; on the other hand, the deposition of carbon could block the active sites and lead to inactivation when the reaction temperature is over 340 degrees C.
引用
收藏
页码:1013 / 1020
页数:8
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