Destruction and defluorination of PFAS matrix in continuous-flow supercritical water oxidation reactor: Effect of operating temperature
Cleanup and disposal of stockpiles and waste streams containing per- and polyfluoroalkyl substances (PFAS) require effective end-of-life destruction/mineralization technologies. Two classes of PFAS, perfluoroalkyl carboxylic acids (PFCAs) and perfluoroalkyl sulfonic acids (PFSAs), are commonly found...
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Veröffentlicht in: | Chemosphere (Oxford) 2023-06, Vol.327, p.138358-138358, Article 138358 |
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Sprache: | eng |
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Zusammenfassung: | Cleanup and disposal of stockpiles and waste streams containing per- and polyfluoroalkyl substances (PFAS) require effective end-of-life destruction/mineralization technologies. Two classes of PFAS, perfluoroalkyl carboxylic acids (PFCAs) and perfluoroalkyl sulfonic acids (PFSAs), are commonly found in legacy stockpiles, industrial waste streams, and as environmental pollutants. Continuous flow supercritical water oxidation (SCWO) reactors have been shown to destroy several PFAS and aqueous film-forming foams. However, a direct comparison of the SCWO efficacy for PFSAs and PFCAs has not been reported. We show the effectiveness of continuous flow SCWO treatment for a matrix of model PFCAs and PFSAs as a function of operating temperature. PFSAs appear to be significantly more recalcitrant than PFCAs in the SCWO environment. The SCWO treatment results in a destruction and removal efficiency of 99.999% at a T > 610 °C and at a residence time of ∼30 s. Fluoride recovery lags destruction PFAS at 510 °C and reaches >100% above 610 °C, confirming the formation of liquid and gaseous phase intermediate product during lower temperature oxidation. This paper establishes the threshold for destroying PFAS-containing liquids under SCWO conditions.
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•Over 99.999% destruction and removal efficiency (DRE) of PFAS achieved at 650 °C.•All perfluoroalkyl carboxylic acids (PFCAs) destroyed at 510 °C.•Defluorination efficiency lags destruction suggesting formation of intermediate species. |
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ISSN: | 0045-6535 1879-1298 |
DOI: | 10.1016/j.chemosphere.2023.138358 |