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Determination of three phenoxyacid herbicides in environmental water samples by the application of dispersive liquid-liquid microextraction coupled with micellar electrokinetic chromatography

机译:分散液-液微萃取-胶束电动色谱法测定环境水样中的三种苯氧酸除草剂

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摘要

An efficient method based on dispersive liquid-liquid microextraction coupled with micellar electrokinetic chromatography has been developed for determination of three phenoxyacid herbicides (PAs) of 2,4-dichlorophenoxybutyric acid (2,4-DB), dicamba and 2,4-dichlorophenoxyacetic acid (2,4-D), in environmental water samples. The types and volumes of extracting and dispersing solvents, ionic strength, extraction and centrifugation time and centrifugation speed were investigated. Successful separation of the three PAs was achieved within 7 min, by using the background electrolyte solution consisting of 10 mmol L-1 sodium tetraborate, 25 mmol L-1 sodium dodecyl sulfate and 15% (v/v) methanol, at pH 9.75. Excellent analytical performances were attained, such as good linear relationships (R a parts per thousand yen0.9993) between peak area and concentration for each PAs from 10-1000 ng mL(-1), limits of detection of 1.56-1.91 ng mL(-1), and intra-day precisions at two spiked levels in terms of migration time and peak area within the range of 0.22-0.42% and 3.88-6.39%, respectively. Enrichment factors of 2,4-DB, dicamba and 2,4-D were 180, 151 and 216, respectively. The method recoveries obtained at fortified 20.0, 50.0 and 100.0 ng mL(-1) for lake, river and reservoir water samples varied from 67.91 to 119.07% with the relative standard deviation of 1.47-6.89%.
机译:建立了一种基于分散液-液微萃取结合胶束电动色谱的有效方法,用于测定3种2,4-二氯苯氧基丁酸(2,4-DB),麦草畏和2,4-二氯苯氧基乙酸的苯氧酸除草剂(PAs) (2,4-D),在环境水样品中。研究了萃取和分散溶剂的种类和体积,离子强度,萃取和离心时间以及离心速度。通过使用背景电解质溶液(pH值为9.75,由10 mmol L-1四硼酸钠,25 mmol L-1十二烷基硫酸钠和15%(v / v)甲醇组成)在7分钟内成功分离出三个PA。获得了出色的分析性能,例如10-1000 ng mL(-1)范围内每个PA的峰面积与浓度之间的线性关系良好(R a千分之千日元¥0.9993),检测限为1.56-1.91 ng mL -1),以及在两个尖峰级别的日内精度,分别在迁移时间和峰面积上,在0.22-0.42%和3.88-6.39%的范围内。 2,4-DB,麦草畏和2,4-D的富集因子分别为180、151和216。在湖泊,河流和水库水样品中,以强化浓度20.0、50.0和100.0 ng mL(-1)获得的方法回收率从67.91到119.07%,相对标准偏差为1.47-6.89%。

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