Abstract
Given that only a small number of per- and polyfluoroalkyl substances (PFAS) are routinely monitored, levels of PFAS in the atmosphere may be underestimated. A protocol including analyses of target PFAS (n = 50), water-soluble fluoride, and total fluorine has been proposed and applied to atmospheric samples. The whole method recovery (including extraction recovery and sampling efficiency) of 90–110% were obtained for the majority of compounds (48/50) with low deviations between replicates (< 20%). Fluorotelomer alcohols were the most prevalent PFAS in the indoor air, while the outdoor air was dominated by the ultrashort-chain ionic PFAS (e.g., trifluoroacetic acid and perfluoropropanoic acid). Concentrations of organofluorine (OF) compounds calculated from the fluorine mass balance ranged from 1.74 ng F/m3 to 14.3 ng F/m3 and from 52.0 ng F/m3 to 1100 ng F/m3 in the particulate and gaseous phases, respectively, whereas only a minor proportion (around 1%) could be explained by target PFAS. In indoor air, OF compounds were observed in relatively high levels and with a shift to the fine particles (PM<1). Our results reveal a large proportion of unidentified OF signatures in the atmosphere and suggest the need to use multiple approaches to improve our understanding of airborne fluorinated substances.
| Original language | English |
|---|---|
| Article number | 129025 |
| Journal | Journal of Hazardous Materials |
| Volume | 435 |
| DOIs | |
| Publication status | Published - 5 Aug 2022 |
Keywords
- Gas-particle partitioning
- Organofluorine
- Per- and polyfluoroalkyl substances
- Size-segregated distribution
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