首页> 外文期刊>Analytical chemistry >Part-per-Trillion Determination of Pharmaceuticals, Pesticides, and Related Organic Contaminants in River Water by Solid-Phase Extraction Followed by Comprehensive Two-Dimensional Gas Chromatography Time-of-Flight Mass Spectrometry
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Part-per-Trillion Determination of Pharmaceuticals, Pesticides, and Related Organic Contaminants in River Water by Solid-Phase Extraction Followed by Comprehensive Two-Dimensional Gas Chromatography Time-of-Flight Mass Spectrometry

机译:固相萃取-综合二维气相色谱-飞行时间质谱法测定河水中的药物,农药和相关有机污染物

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摘要

An analytical procedure based on comprehensive two-dimensional gas chromatography (GC X GC) coupled with time-of-flight mass spectrometry (TOF-MS) for the simultaneous determination of 97 organic contaminants at trace concentration in river water is presented. The target analytes included 13 pharmaceuticals, 18 plasticizers, 8 personal care products, 9 acid herbicides, 8 triazines, 10 organophosphorous compounds, 5 phenylureas, 12 organochlorine biocides, 9 polycyclic aromatic hydrocarbons (PAHs), and 5 benzothiazoles and benzotriazoles. The best resolution of the target analytes in the contour plots was obtained when a nonpolar stationary phase was used in the first dimension and polar one in the second. However, in the opposite configuration, polar-nonpolar, the retention time in the second dimension exhibited a strong correlation with the log Kow (p < 0.01), and it was proposed as an additional identification criteria. The developed methodology is based on a polymeric solid-phase extraction followed by in GC-port methylation and GC X GC/TOF-MS determination. Moreover, limits of detection (LODs) and quantification (LOQs) ranged from 0.5 to 100 ng/L and from 2 to 185 ng/L, respectively. Repeatability was always lower than 20percent. Finally, the developed method has been successfully applied to the determination of incurred target analytes in four river waters subjected to a different anthropogenic pressure.
机译:提出了一种基于综合二维气相色谱(GC X GC)结合飞行时间质谱(TOF-MS)的分析方法,该方法可同时测定河水中痕量浓度的97种有机污染物。目标分析物包括13种药物,18种增塑剂,8种个人护理产品,9种酸性除草剂,8种三嗪,10种有机磷化合物,5种苯基脲,12种有机氯杀生物剂,9种多环芳烃(PAH)和5种苯并噻唑和苯并三唑。当在第一维中使用非极性固定相,在第二维中使用极性的固定相时,在等高线图中获得了目标分析物的最佳分辨率。但是,在相反的配置(极性-非极性)中,第二维的保留时间与log Kow呈极强相关性(p <0.01),因此建议将其作为附加的识别标准。所开发的方法基于聚合物固相萃取,然后进行GC端口甲基化和GC X GC / TOF-MS测定。此外,检测限(LOD)和定量限(LOQ)分别为0.5至100 ng / L和2至185 ng / L。重复性始终低于20%。最终,所开发的方法已成功地用于测定四种在不同人为压力下的河流中目标分析物的含量。

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