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Distribution of per- and polyfluoroalkyl substances (PFASs ) in a waste-to-energy plant: tracking PFASs in internal residual streams
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.
Umeå universitet, Teknisk-naturvetenskapliga fakulteten, Kemiska institutionen.ORCID-id: 0000-0001-7589-9653
2024 (engelsk)Inngår i: Environmental Science and Technology, ISSN 0013-936X, E-ISSN 1520-5851, Vol. 58, nr 19, s. 8457-8463Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Per- and polyfluoroalkyl substances (PFASs) constitute a diverse group of man-made chemicals characterized by their water- and oil-repellent properties and persistency. Given their widespread use in consumer products, PFASs will inevitably be present in waste streams sent to Waste-to-Energy (WtE) plants. We have previously observed a subset of PFASs in residual streams (ashes, treated process water, and flue gas) from a WtE plant. However, the transport and distribution of PFASs inside the WtE plant have remained unaddressed. This study is part of a comprehensive investigation to create a synoptic overview of the distribution of PFASs in WtE residues. PFASs were found in all sample types except for boiler ash. The total levels of 18 individual PFASs (Σ18PFASs) in untreated flue gas ranged from 5.2 to 9.5 ng m-3, decreasing with 35% ± 10% after wet flue gas treatment. Σ18PFASs in the condensate ranged from 46 to 50 ng L-1, of which perfluorohexanoic acid (PFHxA) made up 90% on a ng L-1 basis. PFHxA was also dominant in filter ash, where Σ18PFASs ranged from 0.28 to 0.79 ng g-1. This study shows that flue gas treatment can capture some PFASs and transfer them into WtE residues.

sted, utgiver, år, opplag, sider
American Chemical Society (ACS), 2024. Vol. 58, nr 19, s. 8457-8463
Emneord [en]
condensate, flue gas treatment, fly ash, municipal solid waste incineration, PFASs
HSV kategori
Identifikatorer
URN: urn:nbn:se:umu:diva-224268DOI: 10.1021/acs.est.3c10221ISI: 001228067500001PubMedID: 38685907Scopus ID: 2-s2.0-85192070897OAI: oai:DiVA.org:umu-224268DiVA, id: diva2:1857551
Forskningsfinansiär
Bio4EnergyTilgjengelig fra: 2024-05-14 Laget: 2024-05-14 Sist oppdatert: 2025-04-24bibliografisk kontrollert
Inngår i avhandling
1. Exploring the occurrence, distribution and transport of per- and polyfluoroalkyl substances in waste-to-energy plant
Åpne denne publikasjonen i ny fane eller vindu >>Exploring the occurrence, distribution and transport of per- and polyfluoroalkyl substances in waste-to-energy plant
2024 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Alternativ tittel[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.

sted, utgiver, år, opplag, sider
Umeå: Umeå University, 2024. s. 70
Emneord
PFAS, extractable organofluorine, municipal solid waste incineration, flue gas treatment, industrial water treatment, suspect screening, waste stockpile leachate, bottom ash, condensate, fly ash
HSV kategori
Forskningsprogram
Miljökemi
Identifikatorer
urn:nbn:se:umu:diva-229085 (URN)978-91-8070-461-8 (ISBN)978-91-8070-462-5 (ISBN)
Disputas
2024-09-27, Stora Hörsalen (KBE303), KBC-huset, Umeå, 09:00 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2024-09-06 Laget: 2024-09-03 Sist oppdatert: 2024-09-05bibliografisk kontrollert

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