Effect of surface functionalization of cerium-doped MCM-48 on its catalytic performance for liquid-phase free-solvent oxidation of cyclohexane with molecular oxygen

被引:25
|
作者
Fu, Yu
Zhan, Wangcheng [1 ]
Guo, Yanglong
Wang, Yanqin
Liu, Xiaohui
Guo, Yun
Wang, Yunsong
Lu, Guanzhong
机构
[1] E China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
Ce-MCM-48 mesoporous materials; Surface hydrophobicity; Post-functionalization; Cyclohexane oxidation; Free-solvent catalytic reaction; M-CPBA; NANOPARTICLES; EPOXIDATION; REACTIVITY; COMPLEXES; SIEVES;
D O I
10.1016/j.micromeso.2015.05.004
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Ce-doped MCM-48 (Ce-MCM-48) mesoporous molecular sieve was prepared hydrothermally and its surface was modified with organic groups or fluorine, and their physicochemical properties were characterized by XRD, low-temperature N-2 adsorption, TEM, UV-visible and FT-IR spectroscopies, XPS and contact angle measurement. The results indicated that Ce species were highly dispersed on the MCM-48 materials as Ce3+ and Ce4+. After post-functionalization of Ce-MCM-48, the organic groups or fluorine species have been immobilized on the surface of Ce-MCM-48, but the chemical status of Ce species were hardly changed, and the post-functionalization improved the surface hydrophobicity of the Ce-MCM-48 sample. The catalytic activity testing for the oxidation of cyclohexane with molecular oxygen showed that, Ce-MCM-48 after post-functionalization exhibited the higher cyclohexane conversion and selectivity to cyclohexanol and cyclohexanone, 8.9% cyclohexane conversion with 91.2% selectivity to cyclohexanone and cyclohexanol could be achieved over the Ce-MCM-48 with F-modified catalyst, which was attributed to the proper modification of their surface properties including hydrophobicity and polarity. The F-modified catalyst also showed excellent reusability, and its catalytic performance has no obvious deterioration after being repeatedly used five times. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:101 / 107
页数:7
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