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Persistence of selected pesticides and their phenolic transformation products in natural waters using off-line liquid solid extraction followed by liquid chromatographic techniques

机译:脱机液相固体萃取-液相色谱技术在自然水中对选定农药及其酚类转化产物的残留

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The degradation of three organophosphorus pesticides with phenolic type structure (fenitrothion, ethyl-parathion, methylparathion) and pentachlorophenol in natural waters from Porto (Portugal) was studied. Three different types of natural waters (river water, estuarine water and ground water) were spiked with ethyl-parathion, methyl-parathion, fenitrothion and pentachlorophenol at 40 mu g/l level and were exposed outdoor to ambient sunlight and temperature in natural conditions at the Faculty of Pharmacy of Porto during a period up to 7 weeks. Water samples were placed in 11 Pyrex flasks, properly closed. The samples were exposed day and night at these conditions during May and June 1996, the outside temperature being 22 degrees C with 5.5 h of sunlight exposition per day on average during the period studied. In order to monitor the degradation process, 100 ml of water was preconcentrated periodically by means of liquid solid extraction (LSE) using the polymeric sorbent Lichrolut EN from Merck (Darmstadt, Germany) and the extract was determined by liquid chromatography with diode array detection (LC-DAD). The use of LC coupled with mass spectrometry detection (LC-APcI-MS) permitted the unequivocal identification of various degradation products (4-nitrophenol, 3-methyl-4-nitrophenol, paraoxon ethyl, paroxon methyl, fenitrooxon and S-methylisomer of fenitrothion). Half-life for methyl-parathion was of 3 days in ground water and 4 days in both estuarine and river water; half-life for ethyl-parathion was of 2 days in ground and estuarine water and 3 days in river water; values of 1 day and less than 2 h were obtained for fenitrothion and pentachlorophenol, respectively, in all types of water. All transformation products resulted to be more stable than parent compounds except in ground water conditions. Half-lives of 5 and 4 days were calculated for 4-nitrophenol and paraoxon ethyl, respectively, in estuarine and river water. Values of 3 and 4 days were obtained for 3-methyl-4-nitrophenol in estuarine and river water, respectively. (C) 1997 Elsevier Science B.V.
机译:研究了来自葡萄牙波尔图的天然水中三种酚类结构的有机磷农药(杀nitro硫磷,乙基对硫磷,甲基对硫磷)和五氯苯酚的降解情况。向三种不同类型的天然水(河水,河口水和地下水)中加入40μg / l的乙基对硫磷,甲基对硫磷,杀nitro硫磷和五氯苯酚,并使其暴露在室外阳光和自然条件下的温度下。长达7周的时间在波尔图药学院任教。将水样品置于11个Pyrex烧瓶中,并适当密封。在1996年5月和6月期间,在这些条件下昼夜暴露样品,在此期间,室外温度为22摄氏度,平均每天暴露5.5 h。为了监测降解过程,使用来自默克公司(德国达姆施塔特)的聚合物吸附剂Lichrolut EN通过液体固体萃取(LSE)定期预浓缩100毫升水,并通过带有二极管阵列检测的液相色谱法确定萃取液( LC-DAD)。 LC结合质谱检测(LC-APcI-MS)的使用,可以明确鉴定各种降解产物(4-硝基苯酚,3-甲基-4-硝基苯酚,对氧磷乙基,对氧磷甲基,对氧磷和对硫磷的S-甲基异构体)。甲基对硫磷的半衰期在地下水中为3天,在河口和河水中均为4天。乙硫磷的半衰期在地下水和河口水中为2天,在河水中为3天。在所有类型的水中,杀nitro硫酮和五氯苯酚的值分别为1天和不到2小时。除在地下水条件下外,所有转化产物均比母体化合物更稳定。在河口和河水中分别计算了4-硝基苯酚和对氧磷的半衰期5天和4天。河口和河水中的3-甲基-4-硝基苯酚分别获得3天和4天的值。 (C)1997年Elsevier Science B.V.

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