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Degradation and mechanism of hexafluoropropylene oxide dimer acid by thermally activated persulfate in aqueous solutions.
- Source :
-
Chemosphere . Jan2022:Part 2, Vol. 286, pN.PAG-N.PAG. 1p. - Publication Year :
- 2022
-
Abstract
- Hexafluoropropylene oxide dimer acid (HFPO-DA), an alternative of perfluorooctanoic acid (PFOA), has been detected frequently in environmental media worldwide. It has been reported that HFPO-DA is equal to or more toxic than PFOA, as well as more recalcitrant to degradation. In this study, the efficient degradation of HFPO-DA was achieved by the thermally activated persulfate (TAP) system, but the influence of co-contaminants in the field can be significant. The degradation pathways of HFPO-DA were proposed through an integrated approach of experiment and density functional theory (DFT) calculations. CF 3 CF 2 COO− and CF 3 COO−, were the stable intermediates identified by ultra-performance liquid chromatography-quadrupole-time-of-flight-mass spectrometry (UPLC-Q-TOF-MS). Electron transfer, decarboxylation, H abstraction, HF elimination using H 2 O as a catalyst and hydrolysis occurred in different steps of HFPO-DA degradation process, with –COO− as the initial oxidative site attacked by SO 4 −. In addition, the acute toxicity assessment for HFPO-DA degradation in the TAP system performed by Escherichia coli suggested that HFPO-DA was degraded to a level having no adverse effect on the growth of E. coli , and no more toxic intermediates were formed. Overall, this work provides insights for the degradation of HFPO-DA contamination by the TAP system. [Display omitted] • Effective degradation of HFPO-DA could be achieved in the TAP system. • The –COO− group, rather than the etheric bond, was the initial reactive site. • C 2 F 5 COO− and CF 3 COO− were the stable intermediates identified by UPLC-Q-TOF-MS. • DFT was employed to determine the degradation mechanism of HFPO-DA. • No more toxic intermediate byproducts than HFPO-DA were formed. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 00456535
- Volume :
- 286
- Database :
- Academic Search Index
- Journal :
- Chemosphere
- Publication Type :
- Academic Journal
- Accession number :
- 153528389
- Full Text :
- https://doi.org/10.1016/j.chemosphere.2021.131720