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Solvent demulsification-dispersive liquid-liquid microextraction based on solidification of floating organic drop coupled with ultra-high-performance liquid chromatography-tandem mass spectrometry for simultaneous determination of 13 organophosphate esters in aqueous samples

机译:基于悬浮有机液滴固化的溶剂破乳-分散液-液微萃取-超高效液相色谱-串联质谱法同时测定水溶液中的13种有机磷酸酯

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摘要

This study developed a novel method for the determination of 13 organophosphate esters (OPEs) in aqueous samples through the optimization of solvent demulsification-dispersive liquid-liquid microextraction based on solidification of floating organic drop procedure coupled with ultra-high-performance liquid chromatography-tandem mass spectrometry. The proposed method was rapid and accurate and could be used in field applications. Under the most suitable conditions, the limit of detection and limit of quantification ranged from 0.16 ng/L to 20.0 ng/L and from 0.55 ng/L to 66.7 ng/L, respectively. The enrichment factors (EFs) ranged from 30 to 46. The relative standard deviations were less than 15%. The spiked recoveries ranged between 68.2% and 97.7% in the analysis of actual aqueous samples. The proposed method was convenient, environment friendly, and time and solvent saving and could be used in field applications compared with other methods. Various concentrations and types of OPEs were detected in tap water, river water, and effluent of sewage treatment plant. Effluent samples had the highest detected levels and types of OPEs.
机译:本研究开发了一种基于悬浮有机液滴固化与超高效液相色谱-串联的溶剂破乳-分散液-液微萃取的优化方法来测定水性样品中13种有机磷酸酯的新方法质谱。所提出的方法快速准确,可用于现场应用。在最合适的条件下,检出限和定量限分别为0.16 ng / L至20.0 ng / L和0.55 ng / L至66.7 ng / L。富集因子(EFs)在30到46之间。相对标准偏差小于15%。在实际含水样品的分析中,加标回收率介于68.2%和97.7%之间。与其他方法相比,该方法简便,环保,省时,省溶剂。在自来水,河水和污水处理厂的废水中检测到各种浓度和类型的OPE。出水样品中检测到的OPE的水平和类型最高。

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