首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Water with low concentration of surfactant in dispersed solvent-assisted emulsion dispersive liquid-liquid microextraction for the determination of organochlorine pesticides in aqueous samples
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Water with low concentration of surfactant in dispersed solvent-assisted emulsion dispersive liquid-liquid microextraction for the determination of organochlorine pesticides in aqueous samples

机译:分散溶剂辅助乳液分散液-液微萃取中表面活性剂浓度低的水用于测定水性样品中的有机氯农药

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A novel sample preparation method, "water with low concentration of surfactant in dispersed solvent-assisted emulsion dispersive liquid-liquid microextraction (WLSEME)", coupled with gas chromatography using an electron capture detector (GC-ECD) was developed for the analysis of the organochlorine pesticides (OCPs), heptachlor, α-endosulfan, 4,4-DDE, 2,4-DDD and endrin, in aqueous samples. A microsyringe is used to withdrew and discharge 10-12μL of the extraction solvent and 60-120μL of water as the dispersed solvent (containing 1mgL~(-1), Tween 80) 4 times within 10s to form a cloudy emulsified solution in the syringe. This is then injected into an 8mL aqueous sample spiked with all above OCPs. Dodecyl acetate and 2-dodecanol were both selected as extraction solvents to optimize their conditions separately. The total extraction time was about 0.5min. Under optimum conditions, using dodecyl acetate (12μL) as extraction solvent, the linear range of the method was 10-1000ngL~(-1) for all OCPs, and the the limits of detection (LODs) ranged from 1 to 5ngL~(-1). The absolute recoveries and relative recoveries were from 20.8 to 43.5% and 83.2 to 109.8% for lake water, and 19.9-49.2% and 85.4-115.9% for seawater respectively. In the second method, 2-dodecanol as extraction solvent, the linear range was from 5 to 5000ngL~(-1) for the target compounds, and the LODs were between 0.5 and 2ngL~(-1). The absolute recoveries and relative recoveries ranged from 25.7 to 42.2% and 96.3-111.2% for sea water, and 22.4-41.9% and 90.7-107.9% for stream water. This could solve several problems, which commonly occur in ultrasound-assisted emulsification micro-extraction (USAEME), dispersive liquid-liquid micro-extraction (DLLME) and other assisted emulsification methods. These problems include analyte degradation, increased solubility of the extraction solvent and analyte, and high toxicity and large volume of the organic solvent used.
机译:开发了一种新颖的样品制备方法,“在分散的溶剂辅助乳液分散液-液微萃取(WLSEME)中使用低浓度的表面活性剂水”,并结合使用电子捕获检测器(GC-ECD)的气相色谱仪进行分析。水性样品中的有机氯农药(OCP),七氯,α-硫丹,4,4-DDE,2,4-DDD和异狄氏剂。用微注射器在10s内抽出10-12μL萃取溶剂和60-120μL水作为分散溶剂(含1mgL〜(-1),Tween 80)4次,以形成混浊的乳化溶液。然后将其注入加有上述所有OCP的8mL水样中。选择乙酸十二烷基酯和2-十二烷醇作为提取溶剂以分别优化其条件。总提取时间约为0.5分钟。在最佳条件下,使用乙酸十二烷基酯(12μL)作为萃取溶剂,该方法的线性范围对于所有OCP均为10-1000ngL〜(-1),检出限(LOD)为1至5ngL〜(- 1)。湖泊水的绝对回收率和相对回收率分别为20.8%至43.5%和83.2%至109.8%,海水的绝对回收率分别为19.9-49.2%和85.4-115.9%。在第二种方法中,以2-十二烷醇为提取溶剂,目标化合物的线性范围为5至5000ngL〜(-1),LODs为0.5至2ngL〜(-1)。海水的绝对回收率和相对回收率分别为25.7%至42.2%和96.3-111.2%,溪流水为22.4-41.9%和90.7-107.9%。这可以解决超声辅助乳化微萃取(USAEME),分散液-液微萃取(DLLME)和其他辅助乳化方法中常见的一些问题。这些问题包括分析物降解,萃取溶剂和分析物的溶解度增加以及所用有机溶剂的毒性高和体积大。

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