Ecology and Environment Research Centre, Department of Natural Science, Manchester Metropolitan University, Manchester, UK; Chemistry Matters, Alberta, Canada.
Ecology and Environment Research Centre, Department of Natural Science, Manchester Metropolitan University, Manchester, UK.
Chemosphere. 2024 Nov;367:143645. doi: 10.1016/j.chemosphere.2024.143645. Epub 2024 Nov 6.
There are now over 7 million recognised per- and polyfluoroalkyl substances (PFAS), however the majority of routine monitoring programmes and policy decisions are based on just a handful of these. There is need for a shift towards gaining a better understanding of the total PFAS present in a sample rather than relying on targeted analysis alone. Total PFAS methods help us to understand if targeted methods are missing a mass of PFAS, but they do not identify which PFAS are missing. Non-targeted methods fill this knowledge gap by using high resolution mass spectrometry to identify the PFAS present in a sample. In this manuscript we use complimentary targeted and non-targeted analysis (NTA) to detect hundreds of PFAS in five freshwater samples obtained from the Northwest of the UK. Targeted analysis revealed PFOA at a maximum concentration of 12,100 ng L, over three orders of magnitude greater than the proposed environmental quality standard (EQS) of 100 ng L. A conservative assessment calculated an average total PFAS concentration of approximately 40 μg L across all samples. A suspect screening approach identified between 1175 (least conservative) to 89 (most conservative) PFAS at confidence level 4. Exploratory data analysis was used to identify 33 PFAS at confidence level 3 and 10 PFAS at a confidence level of 2. Only 8 of these 43 PFAS (representing 17% of the total PFAS peak area) are regularly monitored in the UK as part of the UK DWI 47 PFAS. Our results suggested the presence of a novel group of unsaturated perfluoroalkyl ether carboxylic acids (U-PFECAs) related to EEA-NH a perfluoroalkyl ether carboxylic acid (PFECA), providing an example of the benefits of non-targeted screening. This study highlights the merits of non-targeted methods and demonstrates that future monitoring programmes and regulations would benefit from incorporating a non-targeted element.
现在已经有超过 700 万种被认可的全氟和多氟烷基物质 (PFAS),然而,大多数常规监测计划和政策决策都是基于其中的少数几种物质。因此,我们需要转变思路,从仅仅依赖靶向分析转向更好地了解样品中存在的全氟烷基物质总量。全氟烷基物质总量分析方法可以帮助我们了解靶向方法是否遗漏了大量的 PFAS,但无法确定哪些 PFAS 被遗漏。非靶向方法通过使用高分辨率质谱来识别样品中存在的 PFAS,填补了这一知识空白。在本文中,我们使用互补的靶向和非靶向分析(NTA)来检测从英国西北部获得的五个淡水样本中的数百种 PFAS。靶向分析显示,在最大浓度为 12100ng/L 的情况下,PFOA 的浓度超过了提议的环境质量标准 (EQS) 浓度 100ng/L 三个数量级。采用保守评估方法计算,所有样本的平均总 PFAS 浓度约为 40μg/L。可疑筛选方法在置信度为 4 时确定了 1175 种(最不保守)至 89 种(最保守)PFAS。探索性数据分析用于在置信度为 3 时识别出 33 种 PFAS,在置信度为 2 时识别出 10 种 PFAS。在这 43 种 PFAS 中,只有 8 种(占总 PFAS 峰面积的 17%)作为英国 DWI 47 PFAS 的一部分,定期在英国进行监测。我们的研究结果表明,存在一类与 EEA-NH 相关的新型不饱和全氟烷基醚羧酸(U-PFECAs),为非靶向筛选提供了一个很好的例子。本研究强调了非靶向方法的优点,并表明未来的监测计划和法规将受益于纳入非靶向元素。