首页> 外文期刊>Journal of separation science. >Sequential injection-bead injection-lab-on-valve coupled to high-performance liquid chromatography for online renewable micro-solid-phase extraction of carbamate residues in food and environmental samples
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Sequential injection-bead injection-lab-on-valve coupled to high-performance liquid chromatography for online renewable micro-solid-phase extraction of carbamate residues in food and environmental samples

机译:顺序进样-珠阀进样-实验室进样与高效液相色谱法相结合,用于在线可再生微固相萃取食品和环境样品中的氨基甲酸酯残留

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A sequential injection-bead injection-lab-on-valve system was hyphenated to HPLC for online renewable micro-solid-phase extraction of carbamate insecticides. The carbamates studied were isoprocarb, methomyl, carbaryl, carbofuran, methiocarb, promecarb, and propoxur. LiChroprep? RP-18 beads (25-40 μm) were employed as renewable sorbent packing in a microcolumn situated inside the LOV platform mounted above the multiposition valve of the sequential injection system. The analytes sorbed by the microcolumn were eluted using 80% acetonitrile in 0.1% acetic acid before online introduction to the HPLC system. Separation was performed on an Atlantis C-18 column (4.6× 150 mm, 5 μm) utilizing gradient elution with a flow rate of 1.0 mL/min and a detection wavelength at 270 nm. The sequential injection system offers the means of performing automated handling of sample preconcentration and matrix removal. The enrichment factors ranged between 20 and 125, leading to limits of detection (LODs) in the range of 1-20 μg/L. Good reproducibility was obtained with relative standard deviations of <0.7 and 5.4% for retention time and peak area, respectively. The developed method has been successfully applied to the determination of carbamate residues in fruit, vegetable, and water samples.
机译:依次将珠粒顺序注入阀实验室系统连接到HPLC上,用于在线可再生微固相萃取氨基甲酸酯杀虫剂。所研究的氨基甲酸酯为异丙菌威,灭多威,西维威,呋喃丹,甲硫威,扑灭威和丙氧磷。 LiChroprep? RP-18珠(25-40μm)被用作位于LOV平台内部的微柱中的可再生吸附剂填料,该LOV平台安装在顺序注射系统的多位置阀上方。在线导入HPLC系统之前,使用80%乙腈的0.1%乙酸溶液洗脱被微柱吸附的分析物。使用梯度洗脱在Atlantis C-18色谱柱(4.6×150 mm,5μm)上进行分离,流速为1.0 mL / min,检测波长为270 nm。顺序进样系统提供了自动进行样品预浓缩和基质去除的方法。富集因子的范围在20到125之间,导致检出限(LOD)在1-20μg/ L的范围内。保留时间和峰面积的相对标准偏差分别<0.7和5.4%,获得了良好的重现性。该方法已成功应用于水果,蔬菜和水样中氨基甲酸酯残留的测定。

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