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Sampling and simultaneous determination of volatile per- and polyfluoroalkyl substances in wastewater treatment plant air and water

机译:废水处理厂空气和水中的挥发性全氟和多氟烷基物质的采样和同时测定

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摘要

Volatile per- and polyfluoroalkyl substances (PFASs) are often used as precursors in the synthesis of nonvolatile PFASs. The volatile PFASs, which include the perfluoroalkyl iodides (PFAIs), fluorotelomer iodides (FTIs), fluorotelomer alcohols (FTOHs), fluorotelomer olefins (FTOs), fluorotelomer acrylates (FTACs), and fluorotelomer methacrylates (FTMACs), are often produced starting from the telomerization process. These volatile compounds can be present in the air and water environment and can be transformed into highly persistent perfluoroalkyl carboxylic acids. With the exception of FTOHs, which are well studied, the determination of other volatile PFASs is also of prime importance in studying the sources and fate of PFASs. In this study, a method was developed to determine representative precursor compounds that included PFAIs, FTIs, FTOs, FTACs, and FTMACs in wastewater treatment plant (WWTP) air and water samples. The sampling and sample preparation step involved the use of solid-phase extraction (SPE) cartridges with HLB™ material to enrich the analyte. Gas chromatography with mass spectrometry was employed for the detection and quantification of the analytes. Method validation results showed high linearity and sensitivity in the positive electron ionization-selected ion monitoring mode (+EI-SIM). The absolute instrumental limits of detection were in the range of 0.5 to 2 pg. The method detection limit (MDL) in air was 1 ng/m3 with the exception of the FTACs which could be only be detected at concentrations higher than 40 ng/m3. The MDL in water was 10 ng/L. Direct spiking of the cartridges and analyte introduction by volatilization from the glass surface onto the SPE material had recoveries between 86 and 100%. The volatile PFASs were shown to readily partition into the air rather than into water. Consequently, large losses in the amount of PFASs were observed when these were spiked into the water. >Graphical abstractWastewater treatment plant air and water samples were passed through HLB™ solid-phase materials. The eluates were injected onto a GC-MS system to simultaneously determine the volatile PFASs.
机译:易挥发的全氟烷基物质和多氟烷基物质(PFAS)通常用作非挥发性PFAS合成的前体。挥发性PFAS通常是从端粒化过程。这些挥发性化合物可以存在于空气和水环境中,并且可以转化为高度持久的全氟烷基羧酸。除了已得到充分研究的FTOH外,其他挥发性PFAS的测定在研究PFAS的来源和命运方面也至关重要。在这项研究中,开发了一种方法来确定废水处理厂(WWTP)空气和水中样品中包括PFAI,FTI,FTO,FTAC和FTMAC的代表性前体化合物。采样和样品制备步骤涉及使用带有HLB™材料的固相萃取(SPE)柱,以富集分析物。采用质谱气相色谱法检测和定量分析物。方法验证结果表明,在正电子电离选择离子监测模式(+ EI-SIM)下,线性度和灵敏度均很高。仪器的绝对检测极限在0.5至2 pg的范围内。空气中的方法检出限(MDL)为1 ng / m 3 ,但FTAC除外,只能以高于40 ng / m 3 的浓度进行检测。水中的MDL为10 ng / L。柱的直接加标和通过从玻璃表面挥发到SPE材料上的分析物引入具有86%至100%的回收率。挥发性PFASs易于分配到空气中而不是水中。因此,当将PFAS掺入水中时,会发现大量的PFAS损失。 <!-fig ft0-> <!-fig @ position =“ anchor” mode =文章f4-> <!-fig mode =“ anchred” f5-> >图形摘要<!-无花果/图形|无花果/替代品/图形mode =“ anchored” m1-> <!-标题a7->废水处理厂的空气和水样品通过HLB™固相材料。将洗脱液注入GC-MS系统中,同时测定挥发性PFAS。

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