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HERO ID
5083612
Reference Type
Journal Article
Title
Electrochemical oxidation of 6:2 fluorotelomer sulfonic acid (6:2 FTSA) on BDD: electrode characterization and mechanistic investigation
Author(s)
Carrillo-Abad, J; Perez-Herranz, V; Urtiaga, Ane
Year
2018
Is Peer Reviewed?
1
Journal
Journal of Applied Electrochemistry
ISSN:
0021-891X
EISSN:
1572-8838
Publisher
Springer Netherlands
Volume
48
Issue
6
Page Numbers
589-596
Language
English
DOI
10.1007/s10800-018-1180-8
Web of Science Id
WOS:000432525500005
Abstract
6:2 Fluorotelomer sulfonic acid (6:2 FTSA) is used as surfactant and foam stabilizer in the formulation of air firefighting foams (AFFFs). 6:2 FTSA is produced as an alternative to persistent and bioaccumulative long-chain perfluoroalkyl compounds. This study investigates the electrochemical degradation of 6:2 FTSA on a boron-doped diamond (BDD) anode. First, the BDD anode was characterized by cyclic voltammetry, revealing that the direct oxidation of 6:2 FTSA occurred at an anodic potential of 2.72 V versus Ag/AgCl (saturated KCl) electrode. Increasing the scan rate resulted in an increased current intensity of the direct oxidation peak, and this relationship was analyzed using the Randles-Sevcik equation to calculate the diffusion coefficient of 6:2 FTSA in aqueous media (D = 4.16 x 10(-6) cm(2) s(-1) at room temperature). This value is in close agreement to the predicted value obtained by the Wilke-Chang correlation. In electrolysis experiments under potentiostatic control, increasing the anode potential over 2.72 V greatly enhanced the 6:2 FTSA removal, and the simultaneous formation of short-chain perfluorocarboxylic acids (perfluorohexanoic acid, perfluorpentanoic acid and perfluorobutanoic acid) and fluoride release were observed. Based on these observations, the 6:2 FTSA degradation pathway was predicted to start by the attack of hydroxyl radicals to the non-fluorinated carbons to form a perfluorocarboxylate, followed by a single electron transfer to the anode to yield a reactive radical C(6)F(13)COOaEuro . The latter species decarboxylated and finally combined with hydroxyl radicals to allow defluorination to form shorter-chain perfluorocarboxylic acids. [GRAPHICS] .
Keywords
6:2 FTSA; Boron-doped diamond (BDD) anode; Electrolysis; Poly and perfluoroalkyl substances (PFASs)
Tags
PFAS
•
Expanded PFAS SEM (formerly PFAS 430)
Litsearch: September 2019
Web of Science
Not prioritized for screening
6:2 Fluorotelomer sulfonic acid
•
PFAS Universe
Data Source
Web of Science
2-(Perfluorohexyl)-1-ethanol 1-(hydrogen sulfate)
3,3,4,4,5,5,6,6,7,7,8,8,8-Tridecafluorooctane-1-sulfonate
6:2 Fluorotelomer sulfonic acid
Perfluorobutanoic acid
Perfluorohexanoic acid
Perfluorooctanoic acid
•
PFBA
Literature Search Update 5/2019
WOS
Scopus: April 2021
•
PFHxA
LitSearch Update: Feb 2018 - May 2019
WoS
Literature Search
WOS
Scopus: April 2021
HAWC
OW - HHRAB
•
PFOA (335-67-1) and PFOS (1763-23-1)
Literature Search Update (2013-2019)
WOS
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