Room-temperature synthesis of ionic covalent organic frameworks for efficient removal of diclofenac sodium from aqueous solution

化学 水溶液 双氯芬酸钠 共价键 离子键合 双氯芬酸 离子液体 化学工程 无机化学 有机化学 离子 色谱法 催化作用 工程类 生物化学
作者
Haoze Li,Cheng Yang,Hai‐Long Qian,Xiu‐Ping Yan
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:306: 122704-122704 被引量:55
标识
DOI:10.1016/j.seppur.2022.122704
摘要

• Cationic covalent organic framework was synthesized at room temperature. • The iCOF showed large adsorption capacity and rapid kinetics for diclofenac sodium adsorpiton. • Adsorption was driven by ion exchange, electrostatic, π-π and hydrogen bond interaction. The excessive use of diclofenac sodium (DCF) has led to environmental and food safety problems. Effective removal of DCF in aqueous environment is of great significance. Ionic covalent organic frameworks (iCOFs) are effective adsorbents for the removal of pollutants due to their unique structure and properties, but conventional synthesis of iCOFs is limited by high temperature and long reaction time. Herein, we report a room-temperature strategy to synthesize iCOFs in 24 h for the first time. The room-temperature synthesized ionic COF (RT-iCOF) shows better crystallinity, lager uptake capacity and faster kinetics than those synthesized at high temperature with long reaction time. The adsorption kinetics, isotherms and thermodynamics, the effects of ionic strength, pH, humic acid, and reusability of RT-iCOF for DCF were studied in detail. The prepared RT-iCOF gave the maximum adsorption capacity of 857.5 mg g −1 , featuring the highest uptake capacity for DCF so far. The adsorption of DCF on the RT-iCOF are driven by ion exchange, π-π interactions, electrostatic and hydrogen bonds interaction. The adsorption efficiency of RT-iCOF for DCF was still above 90% after 5 regeneration cycles. This work also promotes the facile synthesis and application of iCOFs for the removal of pollutants.
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