4.8 Article

Utilizing Pine Needles to Temporally and Spatially Profile Per- and Polyfluoroalkyl Substances (PFAS)

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 56, Issue 6, Pages 3441-3451

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c06483

Keywords

Biomonitoring; contamination; per- and polyfluoroalkyl substances; fluoroethers; ion mobility; mass spectrometry; PFAS

Funding

  1. National Institutes of Health [P30 ES025128, P42 ES027704, P42 ES031009, T32 GM00876, T32 ES007329]
  2. United States Environmental Protection Agency [STAR RD 84003201]

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As concerns over exposure to PFAS continue to rise, novel monitoring methods are needed. This study used pine needles as passive samplers and a multidimensional analytical method to detect over 70 PFAS in the needles. The results provide critical insights into PFAS transport, contamination, and reduction efforts over the past six decades.
As concerns over exposure to per- and polyfluoroalkyl substances (PFAS) are continually increasing, novel methods to monitor their presence and modifications are greatly needed, as some have known toxic and bioaccumulative characteristics while most have unknown effects. This task however is not simple, as the Environmental Protection Agency (EPA) CompTox PFAS list contains more than 9000 substances as of September 2020 with additional substances added continually. Nontargeted analyses are therefore crucial to investigating the presence of this immense list of possible PFAS. Here, we utilized archived and field-sampled pine needles as widely available passive samplers and a novel nontargeted, multidimensional analytical method coupling liquid chromatography, ion mobility spectrometry, and mass spectrometry (LC-IMS-MS) to evaluate the temporal and spatial presence of numerous PFAS. Over 70 PFAS were detected in the pine needles from this study, including both traditionally monitored legacy perfluoroalkyl acids (PFAAs) and their emerging replacements such as chlorinated derivatives, ultrashort chain PFAAs, perfluoroalkyl ether acids including hexafluoropropylene oxide dimer acid (HFPO-DA, GenX) and Nafion byproduct 2, and a cyclic perfluorooctanesulfonic acid (PFOS) analog. Results from this study provide critical insight related to PFAS transport, contamination, and reduction efforts over the past six decades.

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