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超声辅助乳化-微萃取的正交数组优化及其在河水中氯苯氧乙酸类除草剂测定中的应用。

Orthogonal array optimization of ultrasound-assisted emulsification-microextraction for the determination of chlorinated phenoxyacetic acids in river water.

机构信息

Department of Chemistry, Soochow University, Taipei, Taiwan.

出版信息

J Chromatogr A. 2010 May 21;1217(21):3467-72. doi: 10.1016/j.chroma.2010.03.039. Epub 2010 Mar 27.

Abstract

Orthogonal array design (OAD) was utilized for the first time to optimize the experimental conditions of ultrasound-assisted emulsification-microextraction (USAEME) for determining chlorinated phenoxyacetic acids (CPAs) in river water samples. The use of ultrasound facilitates the mass transfer of CPAs from an aqueous phase into a water-immiscible organic extraction solvent (dichloromethane, DCM) without adding dispersive solvent to form numerous microdroplets. The water-immiscible extractant was collected by centrifugation, dried under low pressure, reconstituted in methanol-water mixture (1:1), and injected into a HPLC system for the determination of CPAs. The linear range was 2-1000 ng mL(-1) (2, 5, 10, 50, 200, 500 and 1000 ng mL(-1)) for each analyte and the relative standard deviations of CPAs among the seven different concentrations were in the range of 1.5-17.0% (n=3). The detection limits (signal-to-noise ratio of 3) of CPAs ranged from 0.67 to 1.50 ng mL(-1). The ranges of intra-day precision (n=3) for CPAs at the levels of 5 and 200 ng mL(-1) were 3.6-11.9% and 5.3-9.5%, respectively. The range of inter-day precision (n=3) at 5 and 200 ng mL(-1) were 1.4-7.7% and 8.5-12.2%, respectively. The applicability of USAEME for environmental analysis was demonstrated by determining CPAs in river water. The recoveries of CPAs from five-spiked river water samples at 10 and 200 ng mL(-1) were 96.3-112.5% and 94.8-109.4%, respectively. The maximum contaminant level (MCL) of 2,4-D in drinking water and the tolerance of residues in food for p-CPA are 70 and 200 microg L(-1), respectively, according to the US EPA regulations. These contaminant levels fall in the linear range investigated in this study. In addition, this USAEME method provided detection limits lower than their contaminant levels, which made USAEME an effective sample preparation method for determining organic environmental contaminants, such as CPAs, in river water samples with little consumption of organic solvent.

摘要

正交实验设计(OAD)首次被用于优化超声辅助乳化微萃取(USAEME)测定河水中氯苯氧乙酸(CPAs)的实验条件。超声的使用有助于 CPAs 从水相向水不溶性有机萃取溶剂(二氯甲烷,DCM)中转移,而无需添加分散溶剂以形成大量微滴。水不溶性萃取剂通过离心收集,在低压下干燥,然后在甲醇-水混合物(1:1)中重构,并注入 HPLC 系统以测定 CPAs。每种分析物的线性范围为 2-1000ngmL(-1)(2、5、10、50、200、500 和 1000ngmL(-1)),七种不同浓度之间 CPAs 的相对标准偏差在 1.5-17.0%(n=3)范围内。CPAs 的检测限(信噪比为 3)范围为 0.67-1.50ngmL(-1)。5 和 200ngmL(-1)水平下 CPAs 的日内精密度(n=3)范围分别为 3.6-11.9%和 5.3-9.5%。5 和 200ngmL(-1)水平下的日间精密度(n=3)范围分别为 1.4-7.7%和 8.5-12.2%。通过测定河水中的 CPAs,证明了 USAEME 用于环境分析的适用性。在 10 和 200ngmL(-1)水平下,从五个加标河水样品中回收 CPAs 的回收率分别为 96.3-112.5%和 94.8-109.4%。根据美国环保署的规定,饮用水中 2,4-D 的最大污染物水平(MCL)和 p-CPA 在食品中的残留允许量分别为 70 和 200μgL(-1)。这些污染物水平处于本研究调查的线性范围内。此外,该 USAEME 方法提供的检测限低于其污染物水平,这使得 USAEME 成为一种有效的样品制备方法,用于测定河水中的有机环境污染物,如 CPAs,且有机溶剂消耗较少。

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