催化学报 ›› 2014, Vol. 35 ›› Issue (11): 1874-1882.DOI: 10.1016/S1872-2067(14)60167-4

• 论文 • 上一篇    下一篇

全氟磺酸功能化碳纳米管的制备及其催化性能

张梦晓, 李璀灿, 华伟明, 乐英红, 高滋   

  1. 复旦大学化学系, 上海市分子催化和功能材料重点实验室, 上海200433
  • 收稿日期:2014-05-03 修回日期:2014-06-10 出版日期:2014-11-06 发布日期:2014-11-06
  • 通讯作者: 乐英红
  • 基金资助:

    国家自然科学基金(20773027,20773028和21273043);上海市科学技术委员会(08DZ2270500).

Preparation and catalytic performance of perfluorosulfonic acid-functionalized carbon nanotubes

Mengxiao Zhang, Cuican Li, Weiming Hua, Yinghong Yue, Zi Gao   

  1. Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Material, Fudan University, Shanghai 200433, China
  • Received:2014-05-03 Revised:2014-06-10 Online:2014-11-06 Published:2014-11-06
  • Supported by:

    This work was supported by the National Natural Science Foundation of China (20773027, 20773028 and 21273043) and the Science & Technology Commission of Shanghai Municipality (08DZ2270500).

摘要:

采用全氟磺酸-全氟乙烯共聚物的液相沉积方法制备了全氟磺酸功能化碳纳米管催化剂, 利用N2吸附、扫描电子显微镜、透射电子显微镜、傅里叶变换红外光谱以及酸碱滴定等方法对材料的结构和酸性进行了表征, 考察了温度和溶剂对催化剂稳定性的影响. 结果表明, 催化剂在极性和非极性溶液中均十分稳定, 并且具有良好的热稳定性, 使用温度可达300 ℃. 该催化剂在对苯二酚与叔丁醇的烷基化反应中表现出优异的催化性能, 其催化活性与稳定性均高于聚苯乙烯磺酸功能化的碳纳米管催化剂.

关键词: 碳纳米管, 全氟磺酸, 酸性, 稳定性, 对苯二酚, 叔丁醇, 烷基化反应

Abstract:

Perfluorosulfonic acid-functionalized carbon nanotubes were prepared by liquid deposition of the perfluorosulfonic acid-polytetrafluoroethylene copolymer and characterized by N2 adsorption, scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, and acid-base titration. The effects of reaction temperature and the type of solvent were investigated. The results showed that these solid acids are very stable in both polar and non-polar solvents and can maintain their acidity up to 300 ℃. Higher activity and better stability were observed over these materials in the alkylation of hydroquinone compared with poly(styrene sulfonic acid)-grafted carbon nanotubes.

Key words: Carbon nanotube, Perfluorosulfonic acid, Acidity, Stability, Hydroquinone alkylation, tert-butanol