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Analysis of PAHs in Water and Fruit Juice Samples by DLLME Combined with LC-Fluorescence Detection

机译:DLLME与LC荧光检测结合用于水和果汁样品中的PAHs分析

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摘要

A simple, rapid and efficient method termed dispersive liquid-liquid microextraction combined with liquid chromatography-fluorescence detection, has been developed for the extraction and determination of polycyclic aromatic hydrocarbons (PAHs) in water and fruit juice samples. Parameters such as the kind and volume of extraction solvent and dispersive solvent, extraction time and salt effect were optimized. Under optimum conditions, the enrichment factors ranged from 296 to 462. The linear range was 0.01-100 mu g L-1 and limits of detection were 0.001-0.01 mu g L-1. The relative standard deviations (RSDs, for 5 mu g L-1 of PAHs) varied from 1.0 to 11.5% (n = 3). The relative recoveries of PAHs from tap, river, well and sea water samples at spiking level of 5 mu g L-1 were 82.6-117.1, 74.9-113.9, 77.0-122.4 and 86.1-119.3%, respectively. The relative recoveries of PAHs from grape and apple juice samples at spiking levels of 2.5 and 5 mu g L-1 were 80.8-114.7 and 88.9-123.0%, respectively. it is concluded that the proposed method can be successfully applied for determination of PAHs in water and fruit juice samples.
机译:已经开发出一种称为分散液-液微萃取结合液相色谱-荧光检测的简单,快速,有效的方法,用于水和果汁样品中多环芳烃(PAHs)的提取和测定。优化了萃取溶剂和分散溶剂的种类和体积,萃取时间和盐分效应等参数。在最佳条件下,富集因子的范围为296至462。线性范围为0.01-100μg L-1,检出限为0.001-0.01μg L-1。相对标准偏差(对于5μg L-1 PAHs,RSDs)从1.0到11.5%(n = 3)变化。加标浓度为5μg L-1时,自来水,河流,井和海水样品中PAHs的相对回收率分别为82.6-117.1%,74.9-113.9、77.0-122.4和86.1-119.3%。峰值浓度为2.5和5μg L-1时,葡萄和苹果汁样品中PAHs的相对回收率分别为80.8-114.7和88.9-123.0%。结论是,该方法可成功用于水和果汁样品中多环芳烃的测定。

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