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首页> 外文期刊>Journal of the Brazilian Chemical Society >A Deep Eutectic Solvent as an Extraction Solvent to Separate and Preconcentrate Parabens in Water Samples Using in situ Liquid-Liquid Microextraction
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A Deep Eutectic Solvent as an Extraction Solvent to Separate and Preconcentrate Parabens in Water Samples Using in situ Liquid-Liquid Microextraction

机译:使用原位液 - 液微萃取在水样中分离和预浓缩的羟基苯甲酸酯的深度共晶溶剂

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摘要

In this study, an in situ deep eutectic solvent-liquid-liquid microextraction method together with high performance liquid chromatography was developed for the determination of parabens in aqueous sample. The hydrophobic deep eutectic solvent, formed in situ by the DL-menthol and decanoic acid was used as the extraction solvent. Various parameters affecting the extraction efficiency including the composition of deep eutectic solvent, temperature of sample solution, extraction time, solution pH and salt concentration were investigated and optimized. Under the optimum conditions, the linear range of calibration curves was in the range of 3-1000 ng mL-1. The limits of detection and limits of quantification were in the range of 0.6-0.8 and 2.0-2.5 ng mL-1, respectively. The relative standard deviations were less than 7.2% for both intra-day and inter-days analysis. Finally, the proposed method was successfully applied to determine four parabens in environmental water samples with acceptable recoveries.
机译:在该研究中,开发了一种与高效液相色谱一起用于测定水性样品中的羟基苯甲酸酯的原位深度共晶溶剂 - 液体微萃取方法。使用DL-METHOL和癸酸原位形成的疏水深浓度溶剂作为萃取溶剂。研究了各种参数,影响提取效率,包括深度共晶溶剂的组成,样品溶液温度,提取时间,溶液pH和盐浓度,并优化。在最佳条件下,校准曲线的线性范围在3-1000ng ml-1的范围内。定量的检测限和限制范围分别为0.6-0.8和2.0-2.5ng ml-1。对于白天和日期的间分析,相对标准偏差小于7.2%。最后,成功地应用了所提出的方法,以确定具有可接受的回收率的环境水样中的四个羟基苯甲酸酯。

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