Melamine-based mesoporous organic polymers as metal-Free heterogeneous catalyst: Effect of hydroxyl on CO2 capture and conversion

被引:68
|
作者
Zhang, Nan [1 ]
Zou, Bo [1 ]
Yang, Guo-Ping [1 ]
Yu, Bing [1 ]
Hu, Chang-Wen [1 ]
机构
[1] Beijing Inst Technol, Sch Chem & Chem Engn, Beijing Key Lab Photoelect Elect, Key Lab Cluster Sci,Minist Educ, Beijing 100081, Peoples R China
基金
中国博士后科学基金;
关键词
Mesoporous organic polymer; Carbon dioxide fixation; Carbon dioxide capture; Hydrogen-bonding; Heterogeneous catalysis; CARBON-DIOXIDE UTILIZATION; HIGHLY EFFICIENT CATALYST; CYCLIC CARBONATES; MICROPOROUS POLYAMINALS; REUSABLE CATALYST; SOLID SORBENT; IONIC LIQUIDS; SURFACE-AREA; FRAMEWORKS; ADSORPTION;
D O I
10.1016/j.jcou.2017.09.001
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of cost-effective heterogeneous catalytic system for the synthesis of organic carbonate from CO2 and epoxide is of great importance. A series of mesoporous organic polymers (MOP-0, MOP-1, MOP-2, and MOP-3) were prepared through facile one-pot polycondensation of commercially available, low-cost melamine and monoaldehydes. These MOPs represent a novel kind of metal-free, recyclable heterogeneous catalysts for the reaction of CO2 with epoxides to form cyclic carbonates through hydrogen-bonding interaction. Moreover, hydroxyl functionalities in MOPs show a critical effect on their performance in CO2 capture and conversion. The CO2 adsorption capacity of these MOPs can be significantly enhanced by increasing the -OH portions in MOPs. Particularly, by introducing -OH group into the MOP structure (MOP-3 vs. MOP-0), the CO2 adsorption capacity under 1 bar at 273 K can be increased by 39% from 82.4 mg g(-1) (MOP-0) to 114.4 mg g(-1) (MOP-3).
引用
收藏
页码:9 / 14
页数:6
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