制备咪唑基多离子液体功能化磁性三维氧化石墨烯,用于茶叶样品中拟除虫菊酯的磁性固相萃取

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Journal of Chromatography B Pub Date : 2024-09-16 DOI:10.1016/j.jchromb.2024.124321
Na Liu, Chuhao Xiao, Weixin Duan, Na Wang, Bo Cui
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引用次数: 0

摘要

本研究采用真空冷冻干燥法合成了咪唑基聚离子液体(聚(1-十二烷基-3-乙烯基-咪唑溴化物))功能化磁性三维氧化石墨烯(Fe3O4@3D-GO@poly(ImC12+Br-)),并将其作为磁性固相萃取(MSPE)吸附剂用于高效萃取茶叶样品中的拟除虫菊酯类农药。通过扫描电子显微镜(SEM)、傅立叶变换红外光谱(FT-IR)、振动样品磁力计(VSM)和 X 射线光电子能谱(XPS)对制备的 Fe3O4@3D-GO@poly(ImC12+Br-) 进行了验证。Fe3O4@3D-GO@poly(ImC12+Br-)具有较大的比表面积,能提供多种分子间相互作用,包括π-π堆叠、疏水和氢键相互作用,因此对拟除虫菊酯具有较高的萃取效率。为提高萃取效率,采用单因素法和盒-贝肯设计法对实验参数进行了优化。在优化条件下,结合高效液相色谱法(HPLC)建立了除虫菊酯类化合物的灵敏分析方法,该方法线性范围宽(1.该方法线性范围宽(1.00-100 μg L-1),相关系数(R)为 0.9980 至 0.9994,检出限低(0.100 μg L-1),重复性好,日内相对标准偏差(RSD)为 2.90-5.53%,日间 RSD 为 1.83-7.76%。此外,该方法还被成功地应用于茶叶样品中拟除虫菊酯类化合物的测定,并获得了82.37%至114.34%的满意回收率。结果表明,所开发的Fe3O4@3D-GO@poly(ImC12+Br-)是一种理想、有效且具有选择性的材料,可用于茶叶样品中拟除虫菊酯类化合物的提取和富集。
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Preparation of an imidazolium-based poly(ionic liquid) functionalized magnetic three-dimensional graphene oxide for magnetic solid phase extraction of pyrethroids from tea samples

In this work, an imidazolium-based poly(ionic liquid) (poly(1-dodecyl-3-vinyl-imidazolium bromide) functionalized magnetic three-dimensional graphene oxide (Fe3O4@3D-GO@poly(ImC12+Br)) was synthesized via a vacuum freezing-drying method and used as a magnetic solid phase extraction (MSPE) adsorbent for the efficient extraction of pyrethroid pesticides from tea samples. The prepared Fe3O4@3D-GO@poly(ImC12+Br) was confirmed by scanning electron microscopy (SEM), Fourier transform infrared spectrometry (FT-IR), vibrating sample magnetometer (VSM) and X-ray photoelectron spectrogram (XPS). Due to its large specific surface area and the ability to offer multiple intermolecular interactions, including π-π stacking, hydrophobic and hydrogen bond interactions, the prepared Fe3O4@3D-GO@poly(ImC12+Br) showed high extraction efficiency for pyrethroids. The experimental parameters were optimized by a combination of single-factor method and Box-Behnken design to improve the extraction efficiency. Under the optimum conditions, coupled with high performance liquid chromatography (HPLC), a sensitive analytical method was developed for the determination of pyrethroids, and the proposed method showed wide linear ranges (1.00–100 μg L−1) with correlation coefficients (R) ranging from 0.9980 to 0.9994, low limits of detection (0.100 μg L−1) and good repeatability with intra-day relative standard deviations (RSDs) in the range of 2.90–5.53 % and inter-day RSDs in the range of 1.83–7.76 %. Moreover, the developed method was successfully applied to the determination of pyrethroids in tea samples and satisfactory recoveries ranging from 82.37 % to 114.34 % were obtained. The results showed that the developed Fe3O4@3D-GO@poly(ImC12+Br) was an ideal, effective and selective material for the extraction and enrichment of pyrethroids from tea samples.

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来源期刊
Journal of Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
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