硫醚
亚胺
共价键
吸附
水溶液
Mercury(编程语言)
选择性
化学
化学工程
共价有机骨架
化学稳定性
材料科学
组合化学
高分子化学
有机化学
催化作用
计算机科学
工程类
程序设计语言
作者
Yiying Zhang,Hui Li,Jianhong Chang,Xinyu Guan,Lingxue Tang,Qianrong Fang,Valentin Valtchev,Yushan Yan,Shilun Qiu
出处
期刊:Small
[Wiley]
日期:2021-02-19
卷期号:17 (22)
被引量:49
标识
DOI:10.1002/smll.202006112
摘要
Abstract Developing functionalized 3D covalent organic frameworks (3D COFs) is critical to broaden their potential applications. However, the introduction of specific functionality in 3D COFs remains a great challenge because most of the functional groups are not compatible with the synthesis conditions. Herein, for the first time 3D thioether‐based COFs (JUC‐570 and JUC‐571) for mercury (Hg 2+ ) removal from aqueous solution is reported. These 3D thioether‐based COFs prepared by the bottom‐up approach display high Hg 2+ uptakes (972 mg g −1 for JUC‐570 and 970 mg g −1 for JUC‐571 at pH = 5), fast adsorption kinetics (distribution coefficient K d value of 2.29 × 10 7 mL g −1 for JUC‐570 and 2.07 × 10 7 mL g −1 for JUC‐571), and favorable selectivity. In particular, JUC‐570 is periodically decorated with isopropyl groups around imine bonds that markedly improve its chemical stability and effectively prevent the pore collapse, and thus endows high Hg 2+ adsorption capacity (619 mg g −1 ) and excellent cycle performance even at pH = 1. This study not only puts forward a new route to construct stable functionalized 3D COFs, but also promotes their potential applications in areas related to the environment.
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