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Organochlorine pesticide contamination of ground water in the city of Hyderabad

机译:海得拉巴市地下水中的有机氯农药污染

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Organochlorine pesticides are ubiquitous and persistent organic pollutants used widely throughout the world. Due to the extensive use in agriculture, organic environmental contaminants such as HCH, DDT along with other organochlorine pesticides are distributed globally by transport through air and water. The main aim of present study is to determine contamination levels of organochlorine pesticides in the ground water of Hyderabad City. Water samples were collected from 28 domestic well supplies of the city. For this study, random sampling technique was applied, all the samples were collected in high purity glass bottles and refrigerated at 4℃ until analysis. Solid Phase Extraction (SPE) is used for the extraction of organochlorine pesticide residues in water sample. The collected water samples were pre-filtered through a 0.45 μg glass fiber filter (Wattman GF/F) to remove particulate matter and were acidified with hydrochloric acid (6N) to pH 2.5. Methanol modifier (BDH, for pesticide residue analysis, 10 mL) was added to water sample for better extraction. SPE using prepacked reversed phase octadecyl (C-18 bonded silica) contained in cartridges was used for sample preparation. Prior to the extraction, the C-18 bonded phase, which contains 500 mg of bonded phase, was washed with 20 mL methanol. The sample was mixed well and allowed to percolate through the cartridges with flow rate of 10-15 mL/min under vacuum. After sample extraction, suction continued for 15 min to dry the packing material and pesticides trapped in the C-18 bonded phases were eluted by passing 10 mL hexane and fraction was evaporated in a gentle steam of Nitrogen. In all samples pesticide residues were analyzed by GC (Chemito-8510) with Ni~(63) ECD detector. Helium was used as carrier gas and nitrogen was used as make up gas. The injection technique was split/split less. All the samples analyzed were found to be contaminated with four pesticides i.e. DDT, β-Endosulfan, α-Endosulfan and Lindane. DDT was found to range between 0.15 and 0.19 μg L~(-1), β-Endosulfan ranges between 0.21 and 0.87 μg L~(-1), α-Endosulfan ranges between 1.34 and 2.14 μg L~(-1) and Lindane ranges between 0.68 and 1.38 μg L~(-1) respectively. These concentrations of pesticides in the water samples were found to be above their respective Acceptable Daily Intake (ADI) values for Humans.
机译:有机氯农药是在世界各地广泛使用的持久性有机污染物。由于在农业中的广泛使用,六氯环己烷,滴滴涕等有机环境污染物与其他有机氯农药一起通过空气和水运输而在全球范围内分布。本研究的主要目的是确定海得拉巴市地下水中有机氯农药的污染水平。从该市的28口家庭供水中收集了水样。在这项研究中,采用随机抽样技术,将所有样品收集在高纯度玻璃瓶中,并在4℃冷藏直至分析。固相萃取(SPE)用于萃取水样中的有机氯农药残留。收集的水样品通过0.45μg玻璃纤维滤器(Wattman GF / F)进行预过滤,以除去颗粒物,并用盐酸(6N)酸化至pH 2.5。将甲醇改性剂(BDH,用于农药残留分析,10 mL)添加到水样品中,以实现更好的提取。使用装在小柱中的预装反相十八烷基(C-18键合硅胶)的SPE进行样品制备。在萃取之前,将含有500 mg键合相的C-18键合相用20 mL甲醇洗涤。将样品充分混合,并在真空下以10-15 mL / min的流速渗透通过柱子。样品提取后,继续抽吸15分钟以干燥填充材料,并通过使10 mL己烷洗脱捕获在C-18键合相中的农药,并在温和的氮气中蒸发馏分。所有样品中的农药残留均通过带有Ni〜(63)ECD检测器的GC(Chemito-8510)进行分析。氦气用作载气,氮气用作补充气。注射技术的分流/分流较少。发现所有分析的样品都被四种农药污染,即滴滴涕,β-硫丹,α-硫丹和林丹。发现DDT的范围为0.15至0.19μgL〜(-1),β-硫丹的范围为0.21至0.87μgL〜(-1),α-硫丹的范围为1.34至2.14μgL〜(-1)和林丹范围分别在0.68和1.38μgL〜(-1)之间。发现水样品中的这些农药浓度高于其各自的人类可接受的每日摄入量(ADI)值。

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