Journal
CHEMOSPHERE
Volume 327, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2023.138358
Keywords
PFAS; Supercritical water oxidation; Destruction; Defluorination; Waste treatment
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Cleanup and disposal of stockpiles and waste streams containing per- and polyfluoroalkyl substances (PFAS) require effective end-of-life destruction/mineralization technologies. Continuous flow supercritical water oxidation (SCWO) reactors have been shown to effectively destroy PFAS compounds. However, the comparison between the efficacy of SCWO treatment on PFSAs and PFCAs has not been reported.
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 car-boxylic acids (PFCAs) and perfluoroalkyl sulfonic acids (PFSAs), are commonly found in legacy stockpiles, in-dustrial 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 com-parison 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 degrees C and at a residence time of similar to 30 s. Fluoride recovery lags destruction PFAS at 510 degrees C and reaches >100% above 610 degrees 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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