Bipyridinium-Based Ionic Covalent Triazine Frameworks for CO2, SO2, and NO Capture

被引:86
作者
Zhu, Hai [2 ]
Lin, Wenjun [1 ]
Li, Qi [2 ]
Hu, Yin [2 ]
Guo, Siyu [2 ]
Wang, Congmin [1 ]
Yan, Feng [2 ]
机构
[1] Zhejiang Univ, Dept Chem, ZJU NHU United R&D Ctr, Hangzhou 310027, Peoples R China
[2] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Dept Polymer Sci & Engn, Jiangsu Key Lab Adv Funct Polymer Design & Applic, Suzhou 215123, Peoples R China
基金
中国国家自然科学基金;
关键词
ionic covalent triazine frameworks; harmful gases; specific surface area; adsorption; ion-exchange; MESOPOROUS POLY(IONIC LIQUID)S; CARBON CAPTURE; ADSORPTION; SEPARATION; POLYMERS; REMOVAL; DIOXIDE;
D O I
10.1021/acsami.9b15903
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The exploitation of novel porous materials for capturing/adsorption of harmful gases is considered a very promising approach to deal with air pollution. Herein, bipyridinium-based ionic covalent triazine frameworks (ICTFs) were synthesized via ZnCl2-catalyzed ionothermal polymerization. The as-prepared ICTFs had a satisfactory total pore volume and specific surface of approximately 0.4582 cm(3) g(-1) and 1000 m(2) g(-1), respectively. Moreover, the specific surface area, pore size and distribution, and total pore volumes of ICTFs could be adjusted via ion-exchange of the anion. The obtained ICTFs were explored as the adsorbent for the separation/adsorption of the mixed gases (SO2, CO2, NO, and N-2), and they showed the strong adsorption ability for CO2 (2.75 mmol g(-1)), SO2 (9.22 mmol g(-1)), and NO (4.05 mmol g(-1)) at 1 bar and 298 K. This unique design provides a new insight to prepare high-efficiency porous materials for CO2, SO2, and NO capture.
引用
收藏
页码:8614 / 8621
页数:8
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