离子键合
吸附
化学
共价键
化学吸附
酰胺
选择性
亚胺
离子液体
选择性吸附
无机化学
离子交换
化学工程
双功能
亲核细胞
组合化学
亲核加成
结晶度
化学键
有机化学
聚合物
作者
Chaoji Xiong,Yuhan Wang,Kun Liang,Chunhua Wu,Wei Wu,Qian Chen
出处
期刊:Chemsuschem
[Wiley]
日期:2025-09-23
卷期号:18 (22): e202501155-e202501155
被引量:4
标识
DOI:10.1002/cssc.202501155
摘要
Although many covalent organic frameworks (COFs) can reduce Au 3+ to Au 0 , the reduction mechanism is unclear. These COFs are formed by reversible imine bonds, and their adaptation to acidic environments takes long periods of time, which is difficult for chemical synthesis. As a result, it is great to be able to synthesize a new class of amide‐linked (CONH) nano‐COFs with fewer active sites. Although amide‐based COFs have been reported for gold recovery, the COFs are prepared using postmodification techniques (e.g., dynamic nucleophilic exchange and oxidation). In this study, electrically neutral nano‐COF (Nano‐COFA) and ionic nano‐COF (Ionic‐nano‐COFA) linked by amide bonds are synthesized. The recovery of gold by Nano‐COFA (Ionic‐nano‐COFA) is primarily a fast chemisorption process. Nano‐COFA (Ionic‐nano‐COFA) has a maximum adsorption capacity of 1334 (1736) (25 °C), 2044 (2541) (35 °C), and 2933 (3200) (45 °C) mg g −1 , respectively. Selective adsorption and cyclic regeneration experiments demonstrate that the two types of nano‐COFs exhibit high selectivity for gold and reusability. Additionally, the CN bonds act as reducing agents, changing Au 3+ to Au 0 without affecting the crystallinity of the COFs. For the treatment of real electronic wastewater, both types of nano‐COFs show high selectivity and adsorption efficiency.
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