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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Dispersive liquid-liquid microextraction combined with gas chromatography-flame photometric detection - Very simple, rapid and sensitive method for the determination of organophosphorus pesticides in water
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Dispersive liquid-liquid microextraction combined with gas chromatography-flame photometric detection - Very simple, rapid and sensitive method for the determination of organophosphorus pesticides in water

机译:分散液-液微萃取-气相色谱-火焰光度检测-非常简单,快速,灵敏的方法测定水中的有机磷农药

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摘要

A new method was used for the extraction of organophosphorus pesticides (OPPs) from water samples: dispersive liquid-liquid microextraction (DLLME) coupled with gas chromatography-flame photometric detection (GC-FPD). In this extraction method, a mixture of 12.0 mu L chlorobenzene (extraction solvent) and 1.00 mL acetone (disperser solvent) is rapidly injected into the 5.00 mL water sample by syringe. Thereby, a cloudy solution is formed. In fact, the cloudy state is because of the formation of fine droplets of chlorobenzene, which has been dispersed among the sample solution. In this step, the OPPs in water sample are extracted into the fine droplets of chlorobenzene. After centrifuging (2 min at 5000 rpm), the fine droplets of chlorobenzene are sedimented in the bottom of the conical test tube (5.0 +/- 0.3 mu L). Sedimented phase (0.50 mu l) is injected into the GC for separation and determination of OPPs. Some important parameters, such as kind of extraction and disperser solvent and volume of them, extraction time, temperature and salt effect were investigated. Under the optimum conditions, the enrichment factors and extraction recoveries were high and ranged between 789-1070 and 78.9-107%, respectively. The linear range was wide (10-100 000 pg/mL, four orders of magnitude) and limit of detections were very low and were between 3 to 20 pg/mL for most of the analytes. The relative standard deviations (RSDs) for 2.00 mu g/L of OPPs in water with internal standard were in the range of 1.2-5.6% (n = 5) and without internal standard were in the range of 4.6-6.5%. The relative recoveries of OPI's from river, well and farm water at spiking levels of 50, 500 and 5000 pg/mL were 84-125, 88-123 and 93-118%, respectively. The performance of proposed method was compared with solid-phase microextraction (SPNM) and single drop microextraction. DLLME is a very simple and rapid (less than 3 min) method, which requires low volume of sample (5 mL). It also has high enrichment factor and recoveries for extraction of OPPs from water. (c) 2006 Elsevier B.V. All rights reserved.
机译:一种从水样中提取有机磷农药的新方法:分散液-液微萃取(DLLME)和气相色谱-火焰光度检测(GC-FPD)。在这种提取方法中,通过注射器将12.0μL氯苯(提取溶剂)和1.00 mL丙酮(分散剂)的混合物快速注入5.00 mL水样品中。由此,形成浑浊的溶液。实际上,混浊的状态是由于形成了分散在样品溶液中的氯苯细小液滴。在此步骤中,将水样品中的OPP提取到氯苯细小滴中。离心(以5000 rpm的速度离心2分钟)后,氯苯的细小液滴沉积在锥形试管的底部(5.0 +/- 0.3μL)。将沉淀相(0.50μl)注入GC中,以分离和测定OPP。研究了萃取剂,分散剂的种类,用量,萃取时间,温度和盐分效应等重要参数。在最佳条件下,富集因子和提取回收率较高,分别在789-1070和78.9-107%之间。线性范围宽(10-100 000 pg / mL,四个数量级),检出限很低,大多数分析物的检测限在3到20 pg / mL之间。有内标的水中2.00μg / L的OPP的相对标准偏差(RSD)在1.2-5.6%的范围内(n = 5),在没有内标的水中的相对标准偏差在4.6-6.5%的范围内。峰值浓度分别为50、500和5000 pg / mL时,从河流,井和农场用水中的OPI相对回收率分别为84-125、88-123和93-118%。将该方法的性能与固相微萃取(SPNM)和单滴微萃取进行了比较。 DLLME是一种非常简单,快速(不到3分钟)的方法,需要少量样品(5 mL)。它还具有较高的富集因子,可从水中提取OPP进行回收。 (c)2006 Elsevier B.V.保留所有权利。

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