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Optimized synthesis of molecularly imprinted polymers coated magnetic UIO-66 MOFs for simultaneous specific removal and determination of multi types of macrolide antibiotics in water

吸附 弗伦德利希方程 分子印迹聚合物 水溶液 金属有机骨架 化学 沉淀聚合 固相萃取 聚合物 聚合 分子印迹 选择性吸附 萃取(化学) 选择性 化学工程 色谱法 有机化学 自由基聚合 催化作用 工程类
作者
Yiyang Liu,Hengyuan Zhang,Dechang Xie,Huiyu Lai,Qiufeng Qiu,Xiaoguo Ma
出处
期刊:Journal of environmental chemical engineering [Elsevier BV]
卷期号:10 (4): 108094-108094 被引量:38
标识
DOI:10.1016/j.jece.2022.108094
摘要

Macrolide antibiotics (MALs) are widely used in various fields and are resistant to degrade in the water environment, thus constituting potential hazards to human health. In this work, a new composite, molecularly imprinted polymers coated magnetic metal-organic frameworks with carboxyl modification ([email protected]) was selected and characterized, for the simultaneous specific adsorption and determination of five MALs from aqueous solution. It was found that UIO-66-COOH with ligand defects showed better pre-polymerization effect than other matrix materials. The synthesis conditions for the imprinting polymer were optimized via response surface methodology. The characteristics of related materials were studied, and a series of adsorption experiments were carried out. The results showed that the adsorption equilibriums of [email protected] were reached within 1 h, with the total adsorption capacity for the five MALs was 99.05 mg g−1. The pseudo-second-order kinetic model and Freundlich isotherm model could best fit the adsorption process, and the adsorption thermodynamics was controlled by the change of entropy. Adsorption mechanisms were deduced as hydrogen bonding interaction and electrostatic interaction. In addition, [email protected] has good selectivity and reusability. Furthermore, a new detection method for the five MALs was developed, using the prepared material as the adsorbent for magnetic solid-phase extraction, coupled with high-performance liquid chromatography. Under the optimal extraction condition, the limits of detection for five MALs were 3.1–44.6 μg L−1, and the recoveries were 92.9–108.7 % in the determination of real water samples. Therefore, the [email protected] could be the efficient adsorbent for simultaneous selective removal and sensitive determination of multi-residual MALs.
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