Thiol-Ene Click Reaction Modified Triazinyl-Based Covalent Organic Framework for Pb(II) Ion Effective Removal

被引:13
作者
Li, Mingyan [1 ]
Chen, Liangjun [1 ]
Du, Jiawei [1 ,2 ]
Gong, Chengtao [1 ]
Li, Tingting [1 ]
Wang, Jian [1 ]
Li, Feili [3 ]
She, Yuanbin [1 ]
Jia, Jianhong [1 ,2 ]
机构
[1] Zhejiang Univ Technol, Coll Chem Engn, Hangzhou 310014, Peoples R China
[2] Ecoind Innovat Inst ZJUT, Innovat Res Ctr Adv Environm Technol, Quzhou 324400, Peoples R China
[3] Zhejiang Univ Technol, Coll Environm, Hangzhou 310014, Peoples R China
基金
中国国家自然科学基金;
关键词
covalent organic frameworks (COFs); postsynthetic modification(PSM); thiol-ene click reactions; Pb(II)removal; heavy metal capture; EFFICIENT; ADSORPTION; FUNCTIONALIZATION; NI(II);
D O I
10.1021/acsami.3c16227
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
As a common water pollutant, Pb2+ has harmful effects on the nervous, hematopoietic, digestive, renal, cardiovascular, and endocrine systems. Due to the drawbacks of traditional adsorbents such as structural disorder, poor stability, and difficulty in introducing adsorption active sites, the adsorption capacity is low, and it is difficult to accurately study the adsorption mechanism. Herein, vinyl-functionalized covalent organic frameworks (COFs) were synthesized at room temperature, and sulfur-containing active groups were introduced by the click reaction. By precisely tuning the chemical structure of the sulfur-containing reactive groups through the click reaction, we found that the adsorption activity of the sulfhydryl group was higher than that of the sulfur atom in the thioether. Moreover, the incorporation of flexible linking groups was observed to enhance the adsorption activity at the active site. The maximum adsorption capacity of the postmodified COF TAVA-S-Et-SH for Pb-(II) reached 303.0 mg/g, which is 2.9 times higher than that of the unmodified COF. This work not only demonstrates the remarkable potential of the "thiol-ene" click reaction for the customization of active adsorption sites but also demonstrates the remarkable potential of the "thiol-alkene" click reaction to explore the structure-effect relationship between the active adsorption sites and the metal ion adsorption capacity.
引用
收藏
页码:8688 / 8696
页数:9
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