Exploring the integrity of targeted PFASs in extracted wastewater samples during transport and storage stages
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
PubMed
34102491
DOI
10.1016/j.chemosphere.2021.131065
PII: S0045-6535(21)01537-X
Knihovny.cz E-resources
- Keywords
- Full-scan acquisition, Integrity, Occurrence, PFAS, TOF, WWTP,
- MeSH
- Alkanesulfonates MeSH
- Water Pollutants, Chemical * analysis MeSH
- Fluorocarbons * analysis MeSH
- Alkanesulfonic Acids * MeSH
- Environmental Monitoring MeSH
- Wastewater MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Alkanesulfonates MeSH
- Water Pollutants, Chemical * MeSH
- Fluorocarbons * MeSH
- Alkanesulfonic Acids * MeSH
- Waste Water MeSH
Little information exists on the effects of shipping and handling on per- and polyfluoroalkyl substances (PFASs) in environmental samples. Thus, we evaluated the integrity of dried wastewater extracts and the sensitivity of our high-resolution mass spectrometry (HRMS) instrument to perform such analyses by monitoring 13 representative PFASs in samples extracted, evaporated, and stored at room temperature up to one month. Relative to zero-day recoveries of six detected PFASs ranged between 94 and 124% (RSD <38%) for influents, between 88 and 126% (RSD <18%) for effluents after 28 days. Larger variabilities are tentatively associated with the lack of specific mass-labeled standards and the interactions between analytes and remaining matrix components over time. In a second stage, a mix of local and international dry-shipped wastewater samples were analyzed and the same PFASs were quantified. Up to six PFASs were identified, with median concentrations ranging from 1.3 (perfluoro butyl sulfonate (PFBS)) to 7.7 ng/L (perfluoro hexanoic acid (PFHxA)) and from 1.5 (PFBS) to 13.8 ng/L (PFHxA) in local influents and effluents respectively; and from 0.7 (perfluoro hexyl sulfonate (PFHxS)) to 52.8 ng/L (PFHxA) and from 0.5 (PFHxS) to 21.4 ng/L (PFHxA) in Greek influents and effluents, respectively. The importance of this study lies on the need to consider the wider recovery shifts and expanded variability ranges of PFASs derived from the transport and storage times of dried extracts, particularly when applied to HRMS and wide-scope screening approaches.
City of Palo Alto Palo Alto CA 94303 United States
RECETOX Faculty of Science Masaryk University Kamenice 753 5 625 00 Brno Czech Republic
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