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Magnetic retrieval of an extractant: fast ultrasound-assisted emulsification liquid-liquid microextraction for the determination of polycyclic aromatic hydrocarbons in environmental water samples

机译:萃取剂的磁回收:快速超声辅助乳化液液微萃取法测定环境水样品中的多环芳烃

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摘要

A novel two-step extraction technique combining ultrasound-assisted emulsification liquid-liquid microextraction with magnetic retrieval has been developed and applied to the analysis of six polycyclic aromatic hydrocarbons in environmental water samples coupled with high-performance liquid chromatography. The technique involves an initial extraction of the target analytes by ultrasound-assisted emulsification liquid-liquid microextraction into fine droplets of an organic extractant; and a retrieval and separation process of the organic phase from the aqueous solution with highly hydrophobic magnetic particles. In this way, the organic phase containing the analytes is the target of the magnetic retrieval step rather than the analytes directly. A noteworthy feature of the method is the introduction of highly hydrophobic magnetic particles with hierarchical structure for the magnetic retrieval of an extractant. Under the optimized conditions, good linearity ranging from 0.016 to 80 ng L~(-1) was obtained in spiked water samples with correlation coefficients (R~2) ranging from 0.9962 to 0.9998 and low limits of detection ranging from 2.0 to 19.5 ng L~(-1). The proposed method has been validated in the analysis of real water samples with recoveries in the range of 75.4% to 110.5% and relative standard deviations of less than 9.9%.
机译:开发了一种结合超声辅助乳化液液微萃取和磁回收的新型两步萃取技术,并将其应用于高效液相色谱法分析环境水样中的六种多环芳烃。该技术包括通过超声辅助乳化液-液微萃取法将目标分析物初步萃取成有机萃取剂的细小液滴。以及从具有高疏水性磁性颗粒的水溶液中回收和分离有机相的过程。以这种方式,包含分析物的有机相是磁回收步骤的目标,而不是直接的分析物。该方法的一个值得注意的特征是引入了具有分级结构的高度疏水性磁性颗粒,用于提取剂的磁性回收。在优化的条件下,加标水样中的线性良好,范围为0.016至80 ng L〜(-1),相关系数(R〜2)为0.9962至0.9998,检测下限为2.0至19.5 ng L 〜(-1)。该方法已在实际水样分析中得到验证,回收率在75.4%至110.5%之间,相对标准偏差小于9.9%。

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