Preparation of sulfamethoxazole molecularly imprinted polymers based on magnetic metal–organic frameworks/graphene oxide composites for the selective extraction of sulfonamides in food samples

分子印迹聚合物 吸附 朗缪尔吸附模型 金属有机骨架 石墨烯 傅里叶变换红外光谱 选择性 化学 氧化物 分子印迹 材料科学 化学工程 核化学 有机化学 纳米技术 催化作用 工程类
作者
Xiufen Han,Xiaohui Zhang,Lijuan Zhong,Xiao Yu,Zhai Hai-yun
出处
期刊:Microchemical Journal [Elsevier]
卷期号:177: 107259-107259 被引量:37
标识
DOI:10.1016/j.microc.2022.107259
摘要

• A molecularly imprinted polymer based on magnetic metal–organic frameworks/graphene oxide (MOF/MGO@MIP) was successfully prepared. • The MOF/MGO@MIP exhibited favorable adsorption capacity and selectivity towards SMX. • Under the optimum conditions, the MOF/MGO@MIP/HPLC method showed excellent linearity, good recovery and low LOD. • The method has been successfully applied to the determination of trace SAs in food samples. Novel sulfamethoxazole molecularly imprinted polymers based on magnetic metal–organic frameworks/graphene oxide composites (MOF/MGO@MIP) were synthesized using the surface molecular imprinting technique. The scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy and other characterization methods were used to analyze MOF/MGO@MIP. The adsorption performance of MOF/MGO@MIP was studied via adsorption kinetics, adsorption isotherms and selectivity experiments, and then its adsorption mechanism was investigated using various adsorption models. The adsorption results matched well with a quasi-second-order kinetic model and a Langmuir isotherm model, with the maximum adsorption capacity, equilibrium adsorption time and imprinting factor of 42.65 mg g −1 , 120 min and 1.61, respectively. Meanwhile, the MOF/MGO@MIP with excellent recyclability displayed higher adsorption capacity and selectivity than MOF/MGO@NIP. Under the optimal extraction conditions, a method base on MOF/MGO@MIP combined with high-performance liquid chromatography (MOF/MGO@MIP/HPLC-UV) was established to separate and detect trace sulfonamides in honey and milk samples, achieving lower limits of detection (LOD, 0.39–0.47 μg kg −1 ) with an excellent linear correlation (R 2 > 0.9990). The spiked recovery and relative standard deviation (RSD) were 81.38–96.71% and 1.4–6.3%, respectively. Therefore, MOF/MGO@MIP could be regarded as an efficient adsorbent for SAs pretreatment in food samples.
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