Bioremediation of perfluoroalkyl substances (PFAS) by anaerobic digestion: effect of PFAS on different trophic groups and methane production accelerated by carbon materials

dc.commentsCEB55379por
dc.contributor.authorSilva, Ana Ritapor
dc.contributor.authorDuarte, Maria Salomé Lirapor
dc.contributor.authorAlves, M. M.por
dc.contributor.authorPereira, Lucianapor
dc.date.accessioned2022-03-16T10:12:48Z
dc.date.available2022-03-16T10:12:48Z
dc.date.issued2022-03-15
dc.date.updated2022-03-16T09:02:25Z
dc.description.abstractPer- and polyfluoroalkyl substances (PFAS) are recalcitrant pollutants which tend to persist in soils and aquatic environments and their remediation is among the most challenging with respect to organic pollutants. Anaerobic digestion (AD) supplemented with low amounts of carbon materials (CM), acting as electron drivers, has proved to be an efficient process for the removal of organic compounds from wastewater. This work explores the impact of PFAS on different trophic groups in anaerobic communities, and the effect of carbon nanotubes (CNT), activated carbon (AC), and oxidized AC (AC-HNO3), as electron shuttles on the anaerobic bioremoval of these compounds, based on CH4 production. The inhibition of the specific methanogenic activity (SMA) exerted by perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS), at a concentration of 0.1 mg L1, was below 10% for acetoclastic and below 15%, for acetogenic communities. Hydrogenotrophic methanogens were not affected by the presence of PFAS. All CM reduced the negative impact of PFAS on the CH4 production rate, but AC was the best. Moreover, the methanization percentage (MP) of sewage sludge (SS) increased 41% in the presence of PFOS (1.2 g L1) and AC. In addition, AC fostered an increase of 11% in the MP of SS+PFOS, relative to the condition without AC. AC promoted detoxification of PFOA- and PFOS-treated samples by 51% and 35%, respectively, as assessed by Vibrio fischeri assays, demonstrating the advantage of bringing AD and CM together for PFAS remediation.por
dc.description.publicationversioninfo:eu-repo/semantics/publishedVersion
dc.description.sponsorshipThis study was supported by the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UIDB/04469/2020 unit and COMPETE 2020 (POCI-01- 0145-FEDER-006684) and BioTecNorte operation (NORTE-01-0145-FEDER-000004) funded by the European Regional Development Fund under the scope of Norte2020-Programa Operacional Regional do Norte. Ana Rita Silva holds an FCT grant SFRH/BD/131905/2017 and COVID/BD/151951/2021.por
dc.distributioninternationalpor
dc.identifier.articlenumber1895por
dc.identifier.citationSilva, A. R.; Duarte, Maria Salomé; Alves, M. Madalena; Pereira, Luciana, Bioremediation of perfluoroalkyl substances (PFAS) by anaerobic digestion: effect of PFAS on different trophic groups and methane production accelerated by carbon materials. Molecules, 27(6), 1895, 2022por
dc.identifier.doi10.3390/molecules27061895por
dc.identifier.eissn1420-3049por
dc.identifier.pmid35335259por
dc.identifier.urihttps://hdl.handle.net/1822/76539
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherMDPIpor
dc.relationUIDB/04469/2020por
dc.relationSFRH/BD/131905/2017por
dc.relationCOVID/BD/151951/2021por
dc.relation.publisherversionhttps://www.mdpi.com/journal/moleculespor
dc.rightsopenAccesspor
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/por
dc.subjectAnaerobic processespor
dc.subjectActivated carbonpor
dc.subjectCarbon nanotubespor
dc.subjectSewage sludgepor
dc.subjectSpecific methanogenic activitypor
dc.subjectPerfluorooctanoic acidpor
dc.subjectPerfluorooctane sulfonatepor
dc.subject.wosScience & Technologypor
dc.titleBioremediation of perfluoroalkyl substances (PFAS) by anaerobic digestion: effect of PFAS on different trophic groups and methane production accelerated by carbon materialspor
dc.typearticle
dspace.entity.typePublicationen
oaire.citationConferencePlaceSwitzerland
oaire.citationEndPage18por
oaire.citationIssue6por
oaire.citationStartPage1por
oaire.citationVolume27por
oaire.versionVoRpor
sdum.journalMoleculespor

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