首页> 外文期刊>Analytical and Bioanalytical Chemistry >Confirmatory determination of organochlorine pesticides in surface waters using LC/APCI/tandem mass spectrometry⋄
【24h】

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determination

获取原文
获取原文并翻译 | 示例
           

摘要

A confirmatory method for the determination of organochlorine pesticides (OCPs) and their metabolites (endrin, α-endosulfan, β-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 1mM ammonium acetate-acetonitrile. Endrin, α-endosulfan, β-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 μgL−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 0.31to 0.50 μgL−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已经开发了使用液相色谱/ 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1mM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,除了使用选定离子监测的七氯之外。 SPE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。 2005年,泰国巴吞他尼省,在水稻生长季节的稻田附近采集的地表水样品中,所开发的方法成功地用于测定OCPs及其代谢物。在七个样品中有五个检测到硫酸硫丹,其中三个可以定量在0.31至0.50μgL-1范围内。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号