Modified Ti-MWW Zeolite as a Highly Efficient Catalyst for the Cyclopentene Epoxidation Reaction

被引:8
|
作者
Tong, Wen [1 ]
Yin, Jinpeng [1 ]
Ding, Luoyi [1 ]
Xu, Hao [1 ]
Wu, Peng [1 ]
机构
[1] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai, Peoples R China
来源
FRONTIERS IN CHEMISTRY | 2020年 / 8卷
基金
中国国家自然科学基金;
关键词
Ti-zeolite; epoxidation reaction; cyclopentene; micro-environment; diffusion constrains; LIQUID-PHASE OXIDATION; HYDROGEN-PEROXIDE; TITANIUM SILICATE; PERFORMANCE; TS-1; ALKENES; TITANOSILICATE; COMPLEXES; OLEFINS; SITES;
D O I
10.3389/fchem.2020.585347
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The liquid-phase epoxidation of cyclopentene (CPE) was performed in the Ti-zeolite/H(2)O(2)catalytic system for the clean synthesis of cyclopentene oxide. Among all the Ti-zeolites (Ti-Beta, Ti-MOR, Ti-MCM-68, TS-1, TS-2, and Ti-MWW) investigated in the present study, Ti-MWW provided relatively lower CPE conversion of 13% due to the diffusion constrains but a higher CPO selectivity of 99.5%. The catalytic performance of Ti-MWW was significantly enhanced by piperidine (PI) treatment, with the CPE conversion and CPO selectivity increased to 97.8 and 99.9%, respectively. The structural rearrangement upon PI treatment converted the 3-dimensional (3D) MWW structure to a 2D lamellar one, which enlarged the interlayer space and greatly alleviated the diffusion constrains of cyclic cyclopentene. Furthermore, the newly constructed "open site" six-coordinated Ti active sites with PI as the ligand exhibited higher catalytic activity. The two factors contributed to more significant enhancement of the activity upon PI-assisted structural arrangement compared to the cases in linear alkenes.
引用
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页数:12
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