Optimized CO2 Capture of the Zeolitic Imidazolate Framework ZIF-8 Modified by Solvent-Assisted Ligand Exchange

被引:36
|
作者
Abraha, Yuel W. [1 ]
Tsai, Chih-Wei [1 ,2 ]
Niemantsverdriet, J. W. Hans [3 ]
Langner, Ernst H. G. [1 ]
机构
[1] Univ Free State, Dept Chem, ZA-9300 Bloemfontein, South Africa
[2] Univ Free State, Dept Phys, ZA-9300 Bloemfontein, South Africa
[3] Tech Univ Eindhoven, Schuit Inst Catalysis, Dept Chem Engn & Chem, NL-5600 MB Eindhoven, Netherlands
来源
ACS OMEGA | 2021年 / 6卷 / 34期
基金
新加坡国家研究基金会;
关键词
CARBON-DIOXIDE SEPARATION; LINKER EXCHANGE;
D O I
10.1021/acsomega.1c01130
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Zeolitic imidazolate frameworks, like ZIF-8 and related structures, have shown great potential for the capture of carbon dioxide. Modifying their structure by exchanging part of the constituent organic ligands is a proven method for enhancing the capacity to absorb CO2. In this work, we performed solvent-assisted ligand exchange (SALE) on nanosized ZIF-8 (nZIF-8) with a series of functionalized imidazole derivatives (exchange percentages, after 24 h): 2-bromoimidazole (19%), 2-chloroimidazole (29%), 2-trifluoromethylbenzimidazole (4%), 2-mercaptobenzimidazole (4%), and 2-nitroimidazole (54%). The sodalite topology and porosity of nZIF-8 were maintained with all SALE modifications. Low-pressure CO2 adsorption of nZIF-8 (38.5 cm(3) g(-1)) at STP was appreciably enhanced with all mixed-linker SALE products. Using halogenated (-Cl, -Br, and -CF3) imidazole derivatives in a 24 h SALE treatment resulted in increases between 11 and 22% in CO2 adsorption, while the thiol (-SH)- and nitro (-NO2)-functionalized SALE products led to 32 and 100% increases in CO2 uptakes, respectively. These CO2 uptakes were further optimized by varying the SALE treatment time. The SHbIm- and NO(2)Im-exchanged SALE products of nZIF-8 show 87 and 98 cm(3) g(-1) of CO2 uptakes after 60 and 120 h of SALE, respectively. These are record high CO2 adsorptions for all reported ZIF derivatives at low-pressure conditions.
引用
收藏
页码:21850 / 21860
页数:11
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