离子键合
吸附
浸出(土壤学)
离子
离子液体
化学
共价键
共价有机骨架
选择性
无机化学
化学工程
有机化学
催化作用
环境科学
工程类
土壤科学
土壤水分
作者
Jie Zhao,Zelong Qiao,Yuncheng He,Rui Zhang,Han Li,Xuezhen Song,Dapeng Cao,Shitao Wang
标识
DOI:10.1002/anie.202414366
摘要
The existing electronic waste (e‐waste) and leaching solutions generated by industries accumulate significant amounts of gold (Au), even in excess of those in natural minerals. Therefore, the recycling of Au is extremely significant for the potential sustainability of chemical industry. By designing ionic covalent organic frameworks (COFs), here we synthesize a series of Ionic‐COF‐X (X=Cl‐, Br‐, AcO‐, and SO42‐) by anion regulation strategy. All these ionic COFs exhibit ultrahigh gold adsorption efficiency and excellent regeneration. Moreover, anion regulation could indeed affect the Au capture performance. In particular, when Cl‐ ions serve as counter ions, the Au capacity of Ionic‐COF‐Cl could reach 1270.8 mg g‐1. Moreover, in the actual CPU leaching solution test, the selectivity of Ionic‐COF‐Cl towards Au3+ ion hits 39000 and 4600 times higher than that of Cu2+ and Ni2+ ions, respectively, suggesting that the Ionic‐COF‐Cl is a promising material for highly selective recovering gold from actual e‐waste. DFT calculations further reveal that counter ions can regulate the adsorption affinity of ionic COF framework toward Au. In short, this work provides a useful anion regulation strategy to design ionic COFs as a promising platform for gold selective recovery from actual e‐waste.
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