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Confirmatory determination of organochlorine pesticides in surface waters using LC/APCI/tandem mass spectrometry

机译:使用LC / APCI /串联质谱法确证测定地表水中的有机氯农药

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A confirmatory method for the determination of organochlorine pesticides (OCPs) and their metabolites (endrin, alpha-endosulfan, beta-endosulfan, endosulfan sulfate, heptachlor, heptachlor epoxide, 2,4'-DDD, 4,4'-DDD, 2,4'-DDE 4,4'-DDE, 2,4'-DDT, and 4,4'-DDT) in surface waters using liquid chromatography/APCI/tandem mass spectrometry has been developed. Chromatographic separation was carried out on a ChromSpher 5 Pesticide column using a gradient elution with mobile phase 1 mM ammonium acetate-acetonitrile. Endrin, alpha-endosulfan, beta-endosulfan , endosulfan sulfate, heptachlor and heptachlor epoxide were determined in the negative ionization mode, while the rest compounds in positive ionization mode. For the identification of the analytes, two multireaction monitoring transitions were selected per compounds except for the heptachlor which selected ion monitoring was used. The linearity of the optimized method ranges after SPE concentration, from 0.009 to 30.60 mu gL(-1) with correlation coefficients greater than 0.99. The method recovery values varied from 72 to 119 % for the different fortification levels . The developed method was successfully applied to determine OCPs and their metabolites in surface water samples collected near paddy fields in growing season of rice, at year 2005 in Pathumthani province, Thailand. Endosulfan sulfate was detected in five out of seven samples and three of them could be quantitated in the range of 0.31 to 0.50 mu gL(-1).
机译:一种确定性方法,用于测定有机氯农药(OCP)及其代谢物(内啡肽,α-硫丹,β-硫丹,硫酸硫丹,七氯,七氯环氧化物,2,4'-DDD,4,4'-DDD,2,已经开发出使用液相色谱/ APCI /串联质谱法在地表水中的4'-DDE 4,4'-DDE,2,4'-DDT和4,4'-DDT)。色谱分离在ChromSpher 5农药色谱柱上进行,使用流动相1 mM乙酸铵-乙腈进行梯度洗脱。在负电离模式下测定异狄氏剂,α-硫丹,β-硫丹,硫酸硫丹,七氯和七氯环氧化物,其余化合物则在正电离模式下测定。为了鉴定分析物,每个化合物都选择了两个多反应监测转换,除了使用选择离子监测的七氯以外。固相萃取浓缩后,优化方法的线性范围为0.009至30.60μgL(-1),相关系数大于0.99。对于不同的设防水平,方法的回收率从72%到119%不等。该方法成功地用于测定泰国Pathumthani省2005年水稻生长期在稻田附近的地表水样品中的OCP及其代谢物。在七个样本中的五个样本中检测到硫酸硫丹,其中三个样本的定量范围为0.31至0.50μgL(-1)。

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