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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >In-situ metathesis reaction combined with ultrasound-assisted ionic liquid dispersive liquid-liquid microextraction method for the determination of phenylurea pesticides in water samples
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In-situ metathesis reaction combined with ultrasound-assisted ionic liquid dispersive liquid-liquid microextraction method for the determination of phenylurea pesticides in water samples

机译:原位复分解反应-超声辅助离子液体分散液-液微萃取法测定水样中苯脲类农药

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摘要

A novel microextraction technique, named in-situ metathesis reaction, combined with ultrasound-assisted ionic liquid dispersive liquid-liquid microextraction was developed for the determination of five phenylurea pesticides (i.e., diuron, diflubenzuron, teflubenzuron, flufenoxuron, and chlorfluazuron) in environmental water samples. In the developed method, 360 μL LiNTf _2 aqueous solution (0.162 g/mL) was added to the sample solution containing a small amount of [C _6MIM]Cl (0.034 g) to form a water-immiscible ionic liquid, [C _6MIM]NTf _2, as extraction solution. The mixed solutions were placed in an ultrasonic water bath at 150 W for 4 min and centrifuged at 3500 rpm for 10 min to achieve phase separation. After centrifugation, fine droplets of the extractant phase settled to the bottom of the centrifuge tube and were directly injected into the high-performance liquid chromatography system for analysis. The quantity of [C _6MIM]Cl, the molar ratio of [C _6MIM]Cl and LiNTf _2, ionic strength, ultrasound time, and centrifugation time, were optimized using a Plackett-Burman design. Significant factors obtained were optimized by employing a central composite design. The optimized technique provides good repeatability (RSD 2.4 to 3.5%), linearity (0.5 μg/L to 500 μg/L), low LODs (0.06 μg/L to 0.08 μg/L) and great enrichment factor (244 to 268). The developed method can be applied in routine analysis for the determining of phenylurea pesticides in environmental samples.
机译:建立了一种新的微萃取技术,即原位复分解反应,结合超声辅助的离子液体分散液-液微萃取技术,用于测定环境水中的五种苯基脲类农药(即,双嘧磺隆,双氟苯隆,双氟苯磺隆,氟苯恶隆和氯氟隆)样品。在开发的方法中,将360μLLiNTf _2水溶液(0.162 g / mL)添加到含有少量[C _6MIM] Cl(0.034 g)的样品溶液中,以形成与水不混溶的离子液体[C _6MIM] NTf_2,作为提取液。将混合溶液置于150 W的超声波水浴中4分钟,并以3500 rpm离心10分钟以实现相分离。离心后,萃取剂相的细小液滴沉淀到离心管的底部,然后直接注入高效液相色谱系统中进行分析。使用Plackett-Burman设计优化了[C _6MIM] Cl的量,[C _6MIM] Cl和LiNTf _2的摩尔比,离子强度,超声时间和离心时间。通过采用中央复合设计优化了获得的重要因素。经过优化的技术可提供良好的重复性(RSD 2.4至3.5%),线性(0.5μg/ L至500μg/ L),低LOD(0.06μg/ L至0.08μg/ L)和丰富的富集因子(244至268)。该方法可用于常规分析中测定环境样品中的苯脲类农药。

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