Highly active and selective binary catalyst system for the coupling reaction of CO2 and hydrous epoxides

被引:27
作者
Wei, Ren-Jian [1 ]
Zhang, Xing-Hong [1 ]
Du, Bin-Yang [1 ]
Fan, Zhi-Qiang [1 ]
Qi, Guo-Rong [1 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Zhejiang, Peoples R China
基金
美国国家科学基金会;
关键词
Carbon dioxide; Epoxides; Coupling reaction; Double metal cyanide complex; METAL-CYANIDE COMPLEX; CYCLIC CARBONATE SYNTHESIS; QUATERNARY AMMONIUM-SALTS; PROPYLENE-OXIDE; CHEMICAL FIXATION; HETEROGENEOUS CATALYST; CYCLOHEXENE OXIDE; DIOXIDE; EFFICIENT; POLYMERIZATION;
D O I
10.1016/j.molcata.2013.07.014
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
Although most of the zinc-containing catalysts show excellent catalytic activity for the coupling reaction of carbon dioxide (CO2) with epoxides, generally, trace amounts of water in the reaction systems could cause a significant decrease of the catalytic activity. In this work, a nanoporous zinc-cobalt double metal cyanide complex (Zn-Co-III DMCC) with high surface area was synthesized via a modified hydrothermal process using tri-block copolymer EO20PO70EO20 (P123) as the template. When cetyltrimethylammonium bromide (CTAB) was used as the co-catalyst, the Zn-Co-III DMCC/CTAB binary catalyst system could effectively catalyze the coupling reaction of CO2 with hydrous propylene oxide (PO), producing propylene carbonate (PC) with nearly 100% productivity and 100% selectivity. This binary catalyst system could also catalyze the coupling reaction of other commercial epoxides and CO2 without using any solvents with nearly 100% productivity and 100% selectivity. With such new catalyst system, hundreds of ppm water in the reaction system will no longer be the matter. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:38 / 45
页数:8
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