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Determination of Organophosphorus Pesticides in Underground Water by SPE-GC-MS

机译:固相萃取-气相色谱-质谱法测定地下水中的有机磷农药

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摘要

A rapid and effective method is developed for the determination of organophosphorus pesticides (dichiorovos, methyl parathion, malathion, and parathion) in underground water by solid-phase extraction (SPE)-gas chromatography-mass spectrometry. Some important extraction parameters including types of SPE adsorbents, elution solvents, and injection volume of water samples are optimized. The use of Cleanert-PEP polymer SPE column improved higher extraction efficiencies than the C18 SPE column commonly used. Water samples are extracted using Cleanert-PEP as SPE adsorbent and ethyl acetate as elution solvent. Precision values expressed as relative standard deviation for 1 ug/L of spiked water sample are in the range of 1.6-4.0%. Dichlorvos, methyl parathion, malathion, and parathion are linear in the range of 0.1-1.0 ug/L (r2 = 0.9976), 0.1-2.0 ug/L (r2 = 0.9883), 0.1-2.0 ug/L (r2 = 0.9798), and 0.055-1.1 ug/L (r2 = 0.9790), respectively. The limits of detection for spiked water samples are in the range of 4-10 ng/L. The optimized method is applied to the determination of underground water samples. Recoveries are between 59.5% and 94.6% for spiked underground water samples. The benefit of the method developed is rapid, simple, and has good repeatability.
机译:建立了一种快速有效的固相萃取-气相色谱-质谱法测定地下水中有机磷农药(敌敌畏,甲基对硫磷,马拉硫磷和对硫磷)的方法。优化了一些重要的萃取参数,包括SPE吸附剂的类型,洗脱溶剂和水样的进样量。与通常使用的C18 SPE色谱柱相比,使用Cleanert-PEP聚合物SPE色谱柱可提高更高的萃取效率。使用Cleanert-PEP作为SPE吸附剂和乙酸乙酯作为洗脱溶剂萃取水样。以1 ug / L加标水样品的相对标准偏差表示的精度值在1.6-4.0%的范围内。敌敌畏,甲基对硫磷,马拉硫磷和对硫磷在0.1-1.0 ug / L(r2 = 0.9976),0.1-2.0 ug / L(r2 = 0.9883),0.1-2.0 ug / L(r2 = 0.9798)的范围内呈线性分别为0.055-1.1 ug / L(r2 = 0.9790)。加标水样的检出限为4-10 ng / L。优化后的方法应用于地下水样品的测定。加标的地下水样品的回收率在59.5%至94.6%之间。所开发的方法的优点是快速,简单并且具有良好的可重复性。

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