化学
傅里叶变换离子回旋共振
质谱法
磺酰
环境化学
色谱法
高分辨率
有机化学
遥感
地质学
烷基
作者
Silvia Dudášová,Urs Berger,Bettina Seiwert,Thorsten Reemtsma,Oliver J. Lechtenfeld,Qiuguo Fu
标识
DOI:10.1021/acs.est.4c11600
摘要
Per- and polyfluoroalkyl substances (PFAS) are persistent environmental pollutants with many unknown variants, posing potential ecosystem and human health risks. To comprehensively assess PFAS contamination and overcome the challenge of unknown PFAS identification, we combined Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) and liquid chromatography─quadrupole time-of-flight mass spectrometry (LC-QTOF MS) to identify novel and Legacy PFAS in archived bream liver samples collected in Germany between 1996 and 2020. By leveraging the ultrahigh resolution and mass accuracy of FT-ICR MS, we generated a mass list for cross-comparison with common precursor ion features from LC-QTOF MS. We identified 78 PFAS, including 68 classified into 12 homologue groups and 10 that did not fit into any homologue series, encompassing perfluoroalkyl acids, fluorotelomer-based substances, pentafluorosulfide perfluoroalkyl sulfonic acids, polyfluoroalkyl sulfinates, polyfluoroalkyl sulfonyl sulfonamides, and other novel compounds including ionic liquids. Spatial and temporal analysis revealed that perfluoroalkyl phosphinic acids (C6/C6, C6/C8) and polyfluoroalkyl sulfonic acids (n = 10) have a widespread presence, whereas tris(pentafluoroethyl)trifluorophosphate (FAP) and polyfluoroalkyl sulfonyl sulfonamides (n = 6) are more localized or have only recently emerged in specific regions. These findings underscore the need for continued monitoring to comprehensively understand exposure to PFAS and their long-term environmental impact.
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