One-pot synthesis of ethylene glycol by oxidative hydration of ethylene with hydrogen peroxide over titanosilicate catalysts

被引:61
|
作者
Lu, Xinqing [1 ]
Xu, Hao [1 ]
Yan, Jiaying [1 ]
Zhou, Wen-Juan [1 ,2 ]
Liebens, Armin [2 ]
Wu, Peng [1 ]
机构
[1] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
[2] UMI 3464CNRS Solvay, E2P2L, Xin Zhuang Ind Zone, 3066 Jin Du Rd, Shanghai 201108, Peoples R China
关键词
Titanosilicate; Ti-MWW; Oxidative hydration; Ethylene; Ethylene glycol; LIQUID-PHASE EPOXIDATION; TI-MWW; LAMELLAR PRECURSORS; SELECTIVE SYNTHESIS; ALKENE EPOXIDATION; OXIDE HYDRATION; HIGH-EFFICIENCY; SPECTROSCOPY; EPOXIDES; SYSTEMS;
D O I
10.1016/j.jcat.2017.12.002
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
The oxidative hydration of ethylene with aqueous hydrogen peroxide was investigated over various titanosilicate catalysts for the purpose of one-pot synthesis of ethylene glycol (EG). The effect of titanosilicate topology (Ti-MWW, TS-1, Ti-MCM-68 and Ti-MOR), solvent, Ti content, catalyst amount, H2O/H2O2 ratio, reaction temperature and time on the EG production have been studied in detail. The Ti-MWW/H2O2/H2O catalytic system showed the highest EG yield together with high H2O2 conversion and utilization efficiency for the oxidative hydration of ethylene. The mechanism for the titanosilicate-catalyzed hydration of ethylene oxide (EO) has also been considered, which then shed light on the active sites for the second step in the oxidative hydration of ethylene. The catalyst deactivation could be ascribed to that the target product of EG and other heavy by-products with high boiling points were deposited inside the channels. The used Ti-MWW can be reusable when subjected to the regeneration by high temperature calcination. Amine-assisted structural rearrangement of Ti-MWW not only enhanced the catalytic activity but also improved its stability in the oxidative hydration of ethylene. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:89 / 99
页数:11
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