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Analysis of 29 per- and polyfluorinated compounds in water, sediment, soil and sludge by liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法分析水,沉积物,土壤和污泥中的29种全氟和多氟化合物

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Several analytical methods were optimised for he analysis of 29 per- and polyfluoroalkyl substances (PFASs), including perfluorocarboxylic acids, perfluoroalkyl sulphonic acids and t1uorotelomers (FTs), such as sulphonate, saturated carboxylic acid, unsaturated carboxylic acid, sulphonamide and sulphonamide betaine (FTAB), in environmental samples in order to assess pollution by PFASs around heavily contaminated sites. Non-filtered water samples were extracted, purified and pre-concentrated by a solid-phase extraction (SPE) procedure. Solid samples (sediments, soils and sludges) were extracted through solvent extraction under acidic conditions and thereafter purified and pre-concentrated using the same SPE procedure as for the water samples. An ultra-high performance liquid chromatography coupled to tandem mass spectrometry in negative electrospray ionisation mode was employed to separate and detect targeted compounds. Twelve labelled internal standards were used to provide an adequate correction compensating for matrix effects. The limits of quantification (LOQs) were between 4 and 10 ngit in water depending on the analytes. For solid samples, the LOQs were 2 ngig dry weight (dw) in sediments and soils, and 20 ngig dw in sludges for all analytes. A surrogate parameter method based on the carlaoxylaion of perfluoroalkyl acid precursors under basic pH conditions as furthermore implemented to estimate the occurrence of non targeted PFAS compounds. In order to evaluate the reliability of these analytical methods, environmental samples collected around a training area in France, where aqueous fire-fighting foam is used, were analysed. Of all the compounds detected in these environmental samples, 6:2 FTAB was found in the highest concentrations.
机译:优化了几种分析方法,可分析29种全氟和多氟烷基物质(PFAS),包括全氟羧酸,全氟烷基磺酸和全环聚物(FTs),例如磺酸盐,饱和羧酸,不饱和羧酸,磺酰胺和磺酰胺甜菜碱(FTAB) ),以评估PFAS在重度污染场地周围的污染。未过滤的水样通过固相萃取(SPE)程序进行萃取,纯化和预浓缩。通过在酸性条件下通过溶剂萃取来提取固体样品(沉积物,土壤和污泥),然后使用与水样品相同的SPE程序进行纯化和预浓缩。在负电喷雾电离模式下,采用串联质谱联用的超高效液相色谱法分离和检测目标化合物。十二个标记的内标被用来提供足够的校正以补偿基体效应。取决于分析物,水中的定量限(LOQ)在4到10 ngit之间。对于固体样品,所有分析物的最低定量限为沉积物和土壤中的2 ngig干重(dw),而污泥中的LOQ为20 ngig dw。此外,基于碱性条件下全氟烷基酸前体的卡拉氧根的替代参数方法可用于估算非目标PFAS化合物的存在。为了评估这些分析方法的可靠性,分析了在法国一个训练区域周围收集的环境样本,该区域使用了水性灭火泡沫。在这些环境样品中检测到的所有化合物中,发现6:2 FTAB的浓度最高。

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