脱氢
丙烷
介孔材料
催化作用
选择性
间苯二酚
材料科学
柠檬酸
无机化学
化学
比表面积
化学工程
有机化学
工程类
作者
Lei Liu,Qing‐Fang Deng,Agula Bao,Tie‐Zhen Ren,Yuping Liu,Bao Zhaorigetu,Zhong‐Yong Yuan
标识
DOI:10.1016/j.cattod.2011.08.022
摘要
Monolithic mesoporous carbons were prepared through a simple autoclaving method using citric acid as catalyst instead of HCl. The presence of citric acid plays an important role in determining the structural ordering of the resultant mesoporous structure due to the –COOH groups which can enhance hydrogen interaction between structural directing agent of triblock copolymer F127 and polymeric carbon precursor of resorcinol–formaldehyde resins. The obtained carbons have a hexagonal pore system, uniform pore size of ∼5.0 nm and high BET surface area of ∼758 m2/g. The prepared mesoporous carbons were used as catalyst for dehydrogenation of propane, exhibiting high catalytic activity and stability. After 50 h time-on-stream, the propane conversion of 12.1% was observed with propylene selectivity of 95.1% in the direct dehydrogenation process, while the propane conversion of 20.1% with propylene selectivity of 25.8% in oxidative dehydrogenation process. It has been found that the surface basic groups are active sites.
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