首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Deep eutectic solvent-based ultrasound-assisted dispersive liquid-liquid microextraction coupled with high-performance liquid chromatography for the determination of ultraviolet filters in water samples
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Deep eutectic solvent-based ultrasound-assisted dispersive liquid-liquid microextraction coupled with high-performance liquid chromatography for the determination of ultraviolet filters in water samples

机译:基于深度共晶溶剂的超声辅助分散液 - 液体微萃取,高性能液相色谱耦合,用于测定水样中的紫外线过滤器

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In the present study, a simple and rapid sample preparation method designated ultrasound-assisted dispersive liquid-liquid microextraction based on a deep eutectic solvent (DES) followed by highperformance liquid chromatography with ultraviolet (UV) detection (HPLC-UVD) was developed for the extraction and determination of UV filters from water samples. The model analytes were 2,4-dihydroxybenzophenone (BP-1), benzophenone (BP) and 2-hydroxy-4-methoxybenzophenone (BP-3). The hydrophobic DES was prepared by mixing trioctylmethylammonium chloride (TAC) and decanoic acid (DecA). Various influencing factors (selection of the extractant, amount of DES, ultrasound duration, salt addition, sample volume, sample pH, centrifuge rate and duration) on UV filter recovery were systematically investigated. Under optimal conditions, the proposed method provided good recoveries in the range of 90.2-103.5% and relative standard deviations (inter-day and intra-day precision, n=5) below 5.9%. The enrichment factors for the analytes ranged from 67 to 76. The limits of detection varied from 0.15 to 0.30 ngmL(-1), depending on the analytes. The linearities were between 0.5 and 500 ngmL(-1) for BP-1 and BP and between 1 and 500 ngmL(-1) for BP-3, with coefficients of determination greater than 0.99. Finally, the proposed method was applied to the determination of UV filters in swimming pool and river water samples, and acceptable relative recoveries ranging from 82.1 to 106.5% were obtained. (C) 2017 Published by Elsevier B.V.
机译:在本研究中,一种简单且快速的样品制备方法,基于深对共晶溶剂(DES)的简单和快速的样品制备方法指定了超声辅助的分散液 - 液微萃取,然后用紫外线(UV)检测(HPLC-UVD)进行高矿液相色谱(HPLC-UVD)。水样中紫外线滤波器的提取和测定。模型分析物是2,4-二羟基二苯甲酮(BP-1),二苯甲酮(BP)和2-羟基-4-甲氧基二苯甲酮(BP-3)。通过混合三乙基甲基氯化铵(TAC)和癸酸(DECA)制备疏水剂。系统地研究了各种影响因素(选择萃取剂,DES,超声持续时间,盐添加,样品体积,样品pH,离心率和持续时间),得到了UV过滤器恢复的各种影响。在最佳条件下,所提出的方法提供了良好的回收率,范围为90.2-103.5%和相对标准偏差(日内和日内精度,n = 5)低于5.9%。分析物的富集因子范围为67至76.根据分析物,检测限范率为0.15至0.30 ngml(-1)。对于BP-1和BP的线性介于0.5至500 ngmL(-1)之间,BP-3的1至500 ngmL(-1),测定系数大于0.99。最后,将所提出的方法应用于游泳池和河水样品中的UV过滤器的测定,获得的可接受的相对回收率为82.1至106.5%。 (c)2017年由Elsevier B.V发布。

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