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Occurrence of per- and polyfluoroalkyl substances and unidentified organofluorine in leachate from waste-to-energy stockpile: a case study
Umeå University, Faculty of Science and Technology, Department of Chemistry.
Umeå University, Faculty of Science and Technology, Department of Chemistry. Umeå Energi AB, Umeå, Sweden.
Man-Technology-Environment Research Centre (MTM), School of Science and Technology, Örebro University, Örebro, Sweden.
Umeå University, Faculty of Science and Technology, Department of Chemistry.ORCID iD: 0000-0001-7589-9653
2021 (English)In: Chemosphere, ISSN 0045-6535, E-ISSN 1879-1298, Vol. 278, article id 130380Article in journal (Refereed) Published
Abstract [en]

Per- and polyfluoroalkyl substances (PFASs) are a diverse group of chemicals used in consumer products, which will inevitably end up in waste streams. Landfills are widely recognized secondary point sources of PFASs, but other types of waste management sites have received less attention. Therefore, in a case study presented here we investigated releases of PFASs from temporarily stored waste by determining quantities of 34 PFASs in leachate from a Waste-to-Energy stockpile (45 000 ± 2000 tonnes) during five months in 2019. We also measured extractable organofluorine (EOF) to account for PFASs not included in the target list. The mean total concentration of the 34 PFAS (Σ34PFAS) was 211 ± 31 ng/L, and short-chain (C4–C7) perfluorocarboxylic acids (PFCAs) accounted for 56–60% of the total. Moreover, we found that Σ34PFAS only accounted for 12% ± 4% of EOF detected in the leachate. Our results demonstrate that waste stockpiles are previously unexplored sources of PFASs in the environment, and the dominance of short-chain PFCAs is consistent with observed profiles of contaminants in landfill leachates.

Place, publisher, year, edition, pages
Elsevier, 2021. Vol. 278, article id 130380
Keywords [en]
Per- and polyfluorinated substances, PFAS, Unidentified organofluorine, Waste stockpile, Waste-to-Energy
National Category
Environmental Sciences Analytical Chemistry
Identifiers
URN: urn:nbn:se:umu:diva-182354DOI: 10.1016/j.chemosphere.2021.130380ISI: 000659471700106PubMedID: 33823356Scopus ID: 2-s2.0-85103539920OAI: oai:DiVA.org:umu-182354DiVA, id: diva2:1547532
Available from: 2021-04-27 Created: 2021-04-27 Last updated: 2024-09-03Bibliographically approved
In thesis
1. Exploring the occurrence, distribution and transport of per- and polyfluoroalkyl substances in waste-to-energy plant
Open this publication in new window or tab >>Exploring the occurrence, distribution and transport of per- and polyfluoroalkyl substances in waste-to-energy plant
2024 (English)Doctoral thesis, comprehensive summary (Other academic)
Alternative title[sv]
Förekomst och transport av per- och polyfluorerade alkylsubstanser i avfallsförbränning
Abstract [en]

Efficient municipal solid waste (MSW) management promotes resource conservation, climate-change mitigation, public health, and environmental protection. A key aspect of environmental protection within MSW management is ensuring that potential pollutants are not released into the environment. One group of environmental pollutants of global concern is per- and polyfluoroalkyl substances (PFAS). Also known as “forever chemicals”, these are used in a wide variety of consumer products and industrial processes, and are known for their persistence. The fate of PFAS in waste-management processes, such as Waste-to-Energy (WtE), is largely unknown. This thesis aimed to investigate the fate of PFAS in a WtE plant.

Comprehensive sampling was performed to provide a synoptic overview of the occurrence and distribution of PFAS in residual streams, and to investigate the potential emission of PFAS from the WtE process to the environment.

Short-chain (C ≤ 7) perfluorocarboxylic acids were the dominant class of PFAS across all matrices analysed. PFAS was found in leachate from the temporary MSW stockpile located at the WtE plant, as well as in most incineration residues (e.g., bottom ash, condensate, and flue gas) during the incineration of MSW. Co-incineration of sewage sludge from a wastewater treatment plant and MSW (with the former added at 5–8 wt.% of the latter) led to an increase in the concentration of PFAS in all matrices, with the exception of filter ash and stack flue gas.

In general, the wet flue-gas treatment was able to capture some PFAS and transfer them to the in-house process-water treatment; however, further optimisation is required to increase the ability of this treatment to capture the shortest PFAS investigated (perfluorobutanoic acid).

Overall, these findings highlight that some PFAS are not fully degraded during WtE conversion, and that PFAS could enter the environment via both leaching from unburnt MSW and incineration residues.

Place, publisher, year, edition, pages
Umeå: Umeå University, 2024. p. 70
Keywords
PFAS, extractable organofluorine, municipal solid waste incineration, flue gas treatment, industrial water treatment, suspect screening, waste stockpile leachate, bottom ash, condensate, fly ash
National Category
Other Chemistry Topics
Research subject
Miljökemi
Identifiers
urn:nbn:se:umu:diva-229085 (URN)978-91-8070-461-8 (ISBN)978-91-8070-462-5 (ISBN)
Public defence
2024-09-27, Stora Hörsalen (KBE303), KBC-huset, Umeå, 09:00 (English)
Opponent
Supervisors
Available from: 2024-09-06 Created: 2024-09-03 Last updated: 2024-09-05Bibliographically approved

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Björklund, SofieWeidemann, EvaJansson, Stina

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