A novel ionic-liquid-mediated covalent organic framework as a strong electrophile for high-performance iodine removal

被引:10
|
作者
Fu, Jie [1 ]
Liu, Jia-Ying [1 ]
Zhou, Yue-Ru [1 ]
Zhang, Lei [1 ]
Wang, Shuang-Long [1 ]
Qin, Song [1 ]
Fan, Maohong [2 ,3 ]
Tao, Guo-Hong [1 ]
He, Ling [1 ]
机构
[1] Sichuan Univ, Coll Chem, Chengdu 610064, Peoples R China
[2] Univ Wyoming, Coll Engn & Phys Sci, Laramie, WY 82071 USA
[3] Univ Wyoming, Sch Energy Resources, Laramie, WY 82071 USA
关键词
Covalent organic frameworks; Electrophiles; Ionic liquids; Gas adsorption; VOLATILE IODINE; CAPTURE; EFFICIENT; ADSORPTION; STORAGE;
D O I
10.1016/j.cej.2024.150913
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The research on the adsorption and conversion of non-polar gases (carbon dioxide, hydrogen, iodine, etc.) has attracted global attention. Extensive work has revealed the intuitive impact of the heteroatom effect on the adsorption performance of covalent organic framework (COF) adsorbents for non-polar gases. However, more influencing factors must be studied to more precisely design and construct target-specific COF adsorbents. In this work, an underlying influencing factor, local polarity, is discovered, which is defined as the polarity of the functional moiety. Due to the substitution of strong electrophile, the electron cloud distribution of the COF framework is regulated, and the local polarity that better matches the adsorption of target electrophilic gas (iodine) has been observed. The local polarity of COF has been controlled through several strong electrophilic ionic liquids, dramatically improving adsorption performance. The saturated adsorption capacity increases from 1.5 to 5.2 g.g(-1), and the adsorption kinetics index k 80% value increases from 0.51 to 2.69 g.g(-1).h(-1). The insight would support precise chemical regulation of target-specific COF in energy and environment science.
引用
收藏
页数:8
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