首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Determination of triazine herbicides in aqueous samples by dispersive liquid-liquid microextraction with gas chromatography-ion trap mass spectrometry
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Determination of triazine herbicides in aqueous samples by dispersive liquid-liquid microextraction with gas chromatography-ion trap mass spectrometry

机译:分散液液微萃取-气相色谱-离子阱质谱法测定水样中的三嗪类除草剂

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A simple and rapid new dispersive liquid-liquid microextraction technique (DLLME) coupled with gas chromatography-ion trap mass spectrometric detection (GC-MS) was developed for the extraction and analysis of triazine herbicides from water samples. In this method, a mixture of 12.0 mu L chlorobenzene (extraction solvent) and 1.00 mL acetone (disperser solvent) is rapidly injected by syringe into the 5.00 mL water sample containing 4% (w/v) sodium chloride. In this process, triazines in the water sample are extracted into the fine droplets of chlorobenzene. After centrifuging for 5 min at 6000 rpm, the fine droplets of chlorobenzene are sedimented in the bottom of the conical test tube (8.0 +/- 0.3 mu L). The settled phase (2.0 mu L) is collected and injected into the GC-MS for separation and determination of triazines. Some important parameters, viz, type of extraction solvent, identity and volume of disperser solvent, extraction time, and salt effect, which affect on DLLME were studied. Under optimum conditions the enrichment factors and extraction recoveries were high and ranged between 151-722 and 24.2-115.6%, respectively. The linear range was wide (0.2-200 mu g L-1) and the limits of detection were between 0.021 and 0. 12 mu g L-1 for most of the analytes. The relative standard deviations (RSDs) for 5.00 mu g L-1 of triazines in water were in the range of 1.36-8.67%. The performance of the method was checked by analysis of river and tap water samples, and the relative recoveries of triazines from river and tap water at a spiking level of 5.0 mu g L-1 were 85.2-114.5% and 87.8-119.4%, respectively. This method was also compared with solid-phase microextraction (SPME) and hollow fiber protected liquid-phase microextraction (HFP-LPME) methods. DLLME is a very simple and rapid method, requiring less than 3 min. It also has high enrichment factors and recoveries for the extraction of triazines from water. (c) 2007 Elsevier B.V. All rights reserved.
机译:开发了一种简单快速的新型分散液-液微萃取技术(DLLME)和气相色谱-离子阱质谱检测技术(GC-MS),用于从水样中提取和分析三嗪类除草剂。在这种方法中,通过注射器将12.0μL氯苯(萃取溶剂)和1.00 mL丙酮(分散溶剂)的混合物快速注入5.00 mL包含4%(w / v)氯化钠的水样品中。在此过程中,水样品中的三嗪被萃取到氯苯细小滴中。在6000 rpm下离心5分钟后,氯苯的细小液滴沉淀在锥形试管的底部(8.0 +/- 0.3μL)。收集沉淀相(2.0μL),注入到GC-MS中以分离和测定三嗪。研究了影响DLLME的一些重要参数,即萃取溶剂的类型,分散剂的身份和体积,萃取时间和盐效应。在最佳条件下,富集因子和提取回收率较高,分别在151-722和24.2-115.6%之间。线性范围宽(0.2-200μg L-1),检测限在大多数分析物的0.021至0. 12μgL-1之间。水中5.00 µg L-1三嗪的相对标准偏差(RSD)在1.36-8.67%的范围内。通过分析河流和自来水样品来检验该方法的性能,在峰值水平为5.0μg L-1时,河流和自来水中三嗪的相对回收率分别为85.2-114.5%和87.8-119.4%。 。还将该方法与固相微萃取(SPME)和中空纤维保护液相微萃取(HFP-LPME)方法进行了比较。 DLLME是一种非常简单,快速的方法,所需时间少于3分钟。它还具有很高的富集因子和从水中提取三嗪的回收率。 (c)2007 Elsevier B.V.保留所有权利。

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