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Ultra high performance liquid chromatography tandem mass spectrometry for rapid analysis of trace organic contaminants in water

机译:超高效液相色谱串联质谱法快速分析水中的痕量有机污染物

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Background The widespread utilization of organic compounds in modern society and their dispersion through wastewater have resulted in extensive contamination of source and drinking waters. The vast majority of these compounds are not regulated in wastewater outfalls or in drinking water while trace amounts of certain compounds can impact aquatic wildlife. Hence it is prudent to monitor these contaminants in water sources until sufficient toxicological data relevant to humans becomes available. A method was developed for the analysis of 36 trace organic contaminants (TOrCs) including pharmaceuticals, pesticides, steroid hormones (androgens, progestins, and glucocorticoids), personal care products and polyfluorinated compounds (PFCs) using a single solid phase extraction (SPE) technique with ultra-high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC-MS/MS). The method was applied to a variety of water matrices to demonstrate method performance and reliability. Results UHPLC-MS/MS in both positive and negative electrospray ionization (ESI) modes was employed to achieve optimum sensitivity while reducing sample analysis time (<20 min) compared with previously published methods. The detection limits for most compounds was lower than 1.0 picogram on the column while reporting limits in water ranged from 0.1 to 15 ng/L based on the extraction of a 1 L sample and concentration to 1 mL. Recoveries in ultrapure water for most compounds were between 90-110%, while recoveries in surface water and wastewater were in the range of 39-121% and 38-141% respectively. The analytical method was successfully applied to analyze samples across several different water matrices including wastewater, groundwater, surface water and drinking water at different stages of the treatment. Among several compounds detected in wastewater, sucralose and TCPP showed the highest concentrations. Conclusion The proposed method is sensitive, rapid and robust; hence it can be used to analyze a large variety of trace organic compounds in different water matrixes.
机译:背景技术有机化合物在现代社会中的广泛使用及其通过废水的扩散已导致对源水和饮用水的广泛污染。这些化合物中的绝大多数在废水排放口或饮用水中均未受到监管,而痕量某些化合物可能会影响水生野生生物。因此,谨慎地监测水源中的这些污染物,直到获得与人类有关的足够的毒理学数据为止。开发了一种方法,使用单固相萃取(SPE)技术分析36种痕量有机污染物(TOrC),包括药物,农药,类固醇激素(雄激素,孕激素和糖皮质激素),个人护理产品和多氟化合物(PFC)。结合串联质谱(UHPLC-MS / MS)的超高效液相色谱仪。该方法应用于多种水基质,以证明方法的性能和可靠性。结果与以前发表的方法相比,采用正电喷雾电离和负电喷雾电离(ESI)模式的UHPLC-MS / MS可获得最佳灵敏度,同时减少了样品分析时间(<20分钟)。多数化合物的检测限在色谱柱上均低于1.0皮克,而根据1 L样品的提取和浓度至1 mL的报告,水的极限范围为0.1至15 ng / L。大多数化合物在超纯水中的回收率在90-110%之间,而地表水和废水中的回收率分别在39-121%和38-141%之间。该分析方法成功地用于分析处理不同阶段的几种不同水基质(包括废水,地下水,地表水和饮用水)中的样品。在废水中检测到的几种化合物中,三氯蔗糖和TCPP的浓度最高。结论该方法灵敏,快速,鲁棒。因此,它可用于分析不同水基质中的多种痕量有机化合物。

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