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核壳型磁性分子印迹聚合物的合成及其用于苹果样品中吡虫啉的选择性测定。

Synthesis of core-shell magnetic molecularly imprinted polymer for the selective determination of imidacloprid in apple samples.

机构信息

Chinese Academy of Agricultural Sciences (CAAS), Research Institute of Pomology, Liaoning, P. R. China.

Laboratory of Quality and Safety Risk Assessment for Fruit (Xingcheng), Ministry of Agriculture and Rural Affairs, Xingcheng, P. R. China.

出版信息

J Sep Sci. 2019 Jul;42(14):2455-2465. doi: 10.1002/jssc.201900221. Epub 2019 May 20.

Abstract

This work demonstrates the synthesis and characterization of core-shell magnetic molecularly imprinted polymers based on surface imprinting using methacryloyl chloride as a functional monomer for the selective extraction of imidacloprid (template) from apple fruit. The characterization analysis results ensured the successful synthesis of the magnetic molecularly imprinted polymers owing to their heterogeneous structure and good magnetic properties. An isothermal binding test was assessed with a pseudo-second-order kinetic model, and the kinetic results fit well to the Freundlich isothermal model. The polymers exhibited an adsorption capacity of 5.75 mg/g for the target analyte with a good selective extraction ability. In addition, the polymers can be reused several times without significant performance loss. The molecularly imprinted polymers showed good performance in the analysis of spiked apple sample with a linear range of 0.05-1.0 mg/L, a limit of detection of 0.048 mg/L and a limit of quantification of 0.146 mg/L (S/N = 3/10). The recoveries of the samples were 77.66-96.57% and their respective relative standard deviations were 3.36-0.45%. All the results indicated that the proposed method provided good selective extraction, as qualifying the analytical standards.

摘要

这项工作展示了基于表面印迹法用丙烯酰氯作为功能单体合成核壳型磁性分子印迹聚合物,用于从苹果果实中选择性提取吡虫啉(模板)。由于其具有异质结构和良好的磁性能,特征分析结果确保了磁性分子印迹聚合物的成功合成。等温结合试验采用拟二级动力学模型进行评估,动力学结果与 Freundlich 等温模型拟合良好。该聚合物对目标分析物的吸附容量为 5.75 mg/g,具有良好的选择性萃取能力。此外,该聚合物可以重复使用几次而不会显著损失性能。分子印迹聚合物在分析添加苹果样品中的性能良好,线性范围为 0.05-1.0 mg/L,检测限为 0.048 mg/L,定量限为 0.146 mg/L(S/N = 3/10)。样品的回收率为 77.66-96.57%,各自的相对标准偏差为 3.36-0.45%。所有结果表明,所提出的方法提供了良好的选择性提取,符合分析标准。

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