Boron doped diamond electrooxidation of 6:2 fluorotelomers and perfluorocarboxylic acids. Application to industrial wastewaters treatment

The aim of this study was to determine the viability of electrochemical oxidation to degrade and mineralize poly- and perfluoroalkyl substances (PFASs) in wastewaters from an industrial facility dedicated to the production of side-chain-fluorinated polymers and fluorotelomer-based products for fire-...

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Detalhes bibliográficos
Autores: Gómez Ruiz, Beatriz, Gómez Lavín, Sonia|||0000-0002-4355-8683, Diban Gómez, Nazely|||0000-0002-2636-6305, Boiteux, Virginie, Colin, Adeline, Dauchy, Xavier, Urtiaga Mendia, Ana María|||0000-0002-8189-9171
Formato: artículo
Fecha de publicación:2017
País:España
Recursos:Universidad de Cantabria (UC)
Repositorio:UCrea Repositorio Abierto de la Universidad de Cantabria
Idioma:inglés
OAI Identifier:oai:repositorio.unican.es:10902/11108
Acesso em linha:http://hdl.handle.net/10902/11108
Access Level:acceso abierto
Palavra-chave:Poly- and perfluoroalkyl substances (PFASs)
6:2 FTSA and 6:2 FTAB
Perfluorocarboxylic acids
Electrochemical oxidation
Boron doped diamond anode
Industrial wastewater
Descrição
Resumo:The aim of this study was to determine the viability of electrochemical oxidation to degrade and mineralize poly- and perfluoroalkyl substances (PFASs) in wastewaters from an industrial facility dedicated to the production of side-chain-fluorinated polymers and fluorotelomer-based products for fire-fighting foams. 6:2 fluorotelomer sulfonamide alkylbetaine (6:2 FTAB, 1111 μg/L), 6:2 fluorotelomer sulfonic acid (6:2 FTSA, 242.5 μg/L) and 6:2 fluorotelomer sulfonamide propyl N,N dimethylamine (M4, 34.4 μg/L) were the most abundant PFASs in the industrial wastewater, that also contained perfluorocarboxylic acids (ΣPFCAs, 12.2 μg/L), high TOC and chloride as main anion. 2 L samples were treated in bench scale experiments performed at a current density of 50 mA/cm2, in a commercial cell equipped with a boron doped diamond (BDD) anode (70 cm2). 97.1% of the initial PFASs content was removed after 8 h of electrochemical treatment. Furthermore, the TOC removal (82.5%) and the fluoride release confirmed the PFASs mineralization. Based on the evolution of the different PFASs, electrochemical degradation pathways were proposed. Fluorotelomers sulfonamides 6:2 FTAB and M4 would be degraded into 6:2 FTSA, which conversely would give rise to PFHpA and preferentially PFHxA. The latter PFCAs were transformed into shorter-chain PFCAs, and eventually into CO2 and fluoride. The reported results support the technical viability of BDD electrooxidation for the treatment of PFASs in industrial wastewater.