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首页> 外文期刊>International journal of environmental analytical chemistry >Dispersive liquid-liquid microextraction followed by high-performance liquid chromatography for the determination of three carbamate pesticides in water samples
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Dispersive liquid-liquid microextraction followed by high-performance liquid chromatography for the determination of three carbamate pesticides in water samples

机译:分散液-液微萃取-高效液相色谱法测定水样中的三种氨基甲酸酯农药

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摘要

A simple, rapid and efficient method, dispersive liquid-liquid microextraction (DLLME) in conjunction with high-performance liquid chromatography (HPLC), has been developed for the determination of three carbamate pesticides (methomyl, carbofuran and carbaryl) in water samples. In this extraction process, a mixture of 35μL chlorobenzene (extraction solvent) and 1.0 mL acetonitrile (disperser solvent) was rapidly injected into the 5.0 mL aqueous sample containing the analytes. After centrifuging (5 min at 4000 rpm), the fine droplets of chlorobenzene were sedimented in the bottom of the conical test tube. Sedimented phase (20μL) was injected into the HPLC for analysis. Some important parameters, such as kind and volume of extraction and disperser solvent, extraction time and salt addition were investigated and optimised. Under the optimum extraction condition, the enrichment factors and extraction recoveries ranged from 148% to 189% and 74.2% to 94.4%, respectively. The methods yielded a linear range in the concentration from 1 to 1000 μg L~(-1) for carbofuran and carbaryl, 5 to 1000 μg L~(-1) for methomyl, and the limits of detection were 0.5, 0.9 and 0.1 μg L~(-1), respectively. The relative standard deviations (RSD) for the extractio n of 500 μg L~(-1) carbamate pesticides were in the range of 1.8-4.6% (n = 6). This method could be successfully applied for the determination of carbamate pesticides in tap water, river water and rain water.
机译:已经开发了一种简单,快速,高效的方法,即分散液-液微萃取(DLLME)和高效液相色谱(HPLC),用于测定水中样品中的三种氨基甲酸酯农药(甲氧甲基,呋喃丹和西维因)。在该萃取过程中,将35μL氯苯(萃取溶剂)和1.0 mL乙腈(分散剂溶剂)的混合物快速注入含有分析物的5.0 mL水性样品中。离心(以4000 rpm的转速离心5分钟)后,氯苯细小滴沉淀在锥形试管的底部。将沉淀相(20μL)注入HPLC进行分析。研究并优化了萃取和分散剂的种类和体积,萃取时间和加盐量等重要参数。在最佳提取条件下,富集因子和提取回收率分别为148%至189%和74.2%至94.4%。该方法对呋喃丹和西维因的浓度范围为1至1000μgL〜(-1),对甲hom为5至1000μgL〜(-1)呈线性范围,检出限为0.5、0.9和0.1μg L〜(-1)。 500μgL〜(-1)氨基甲酸酯类农药的相对标准偏差(RSD)为1.8-4.6%(n = 6)。该方法可成功用于自来水,河水和雨水中氨基甲酸酯类农药的测定。

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