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Gas Chromatography-Mass Spectrometry Determination of Polycyclic Aromatic Hydrocarbons in Surface Water

机译:气相色谱 - 质谱法测定地表水中多环芳烃的测定

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摘要

The current status and problems of the determination of polycyclic aromatic hydrocarbons (PAHs) in surface waters are discussed. Sixteen unsubstituted PAHs, which are priority pollutants of aquatic ecosystems, are selected as analytes. Gas chromatography-mass spectrometry (GC-MS) ensures the identification of the majority of pollutants using an integrated spectral library and their determation at a level below the maximum permissible concentration (MPC). The conditions for the simultaneous determination of 16unsubstituted PAHs by GC-MS with detection in the selected ion monitoring mode are optimized. PAHs were extracted from a 1-L water sample by ultrasound-assisted liquid-liquid extraction. The main performance characteristics of the procedure were estimated. The lower limit of the analytical range was from 0.5ng/L (benzo(a)pyrene) to 50 ng/L (naphthalene); the upper limit of the analytical range was 250 ng/L for all PAHs. The procedure was tested in model systems and real samples.
机译:讨论了表面水中多环芳烃(PAHS)的当前状态和问题。 十六个未取代的PAHS,作为水生生态系统的优先污染物,被选为分析物。 气相色谱 - 质谱(GC-MS)确保使用集成光谱库的大多数污染物的鉴定及其在低于最大允许浓度(MPC)的水平下的确定。 优化了在所选离子监测模式中通过检测的GC-MS同时测定16UNsubstitedPAHs的条件。 通过超声辅助液 - 液萃取从1 -L水样中提取PAHS。 估计该程序的主要性能特征。 分析范围的下限为0.5ng / l(苯并(a)芘)至50ng / l(萘); 所有PAH的分析范围的上限为250 ng / L. 该过程在模型系统和真实样品中进行了测试。

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