Adsorption of sulfur into an alkynyl-based covalent organic framework for mercury removal

被引:13
作者
Wang, Shenglin [1 ]
Xin, Yingxiang [2 ]
Hu, Hui [1 ]
Su, Xiaofang [1 ]
Wu, Jifeng [1 ]
Yan, Qianqian [1 ]
Qian, Jiaying [1 ]
Xiao, Songtao [3 ]
Gao, Yanan [1 ]
机构
[1] Hainan Univ, Key Lab Minist Educ Adv Mat Trop Isl Resource, 58 Renmin Ave, Haikou 570228, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, 457 Zhongshan Rd, Dalian 116023, Peoples R China
[3] China Inst Atom Energy, Beijing 102413, Peoples R China
基金
中国国家自然科学基金;
关键词
AQUEOUS-SOLUTIONS; CO2; UPTAKE; WATER; HYDROGEN; DESIGN; 2D; CRYSTALLINE; LUMINESCENT; EFFICIENT; SORPTION;
D O I
10.1039/d2ra06838a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Highly efficient removal of Hg(II) has been previously achieved through the adsorption by functionalized covalent organic frameworks (COFs). Among these COFs, thioether groups need to be deliberately introduced into the pores of COFs through either a bottom-up synthesis or post-synthesis strategy. Herein, we report a simple mercury removal strategy that used a stable alkynyl (-C equivalent to C-) based covalent organic framework (TP-EDDA COF) as an adsorbent for Hg(II) removal. Sulfur vapor was first adsorbed by the TP-EDDA COF due to the van der Waals interaction between adsorbed sulfur and alkynyl groups. The Hg(II) removal capability was then evaluated for the sulfur loaded TP-EDDA COF. Our results exhibited a good Hg(II) removal performance for the sulfur loaded TP-EDDA COF. It was deduced that s center dot center dot center dot pi interaction between sulfur atom and the alkynyl groups of the COF skeleton caused an increase in the electron density of sulfur and the electronegative sulfur atoms acted as a soft acid to accept soft-basic Hg(II). This strategy provides a convenient platform for COFs to cope with environmental issues.
引用
收藏
页码:35445 / 35451
页数:7
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