4.2 Article

Degradation and Defluorination of Aqueous Perfluorooctane Sulfonate by Silica-Based Granular Media Using Batch Reactors

Journal

JOURNAL OF ENVIRONMENTAL ENGINEERING
Volume 147, Issue 11, Pages -

Publisher

ASCE-AMER SOC CIVIL ENGINEERS
DOI: 10.1061/(ASCE)EE.1943-7870.0001922

Keywords

Per- and polyfluoroalkyl substance (PFAS); Aqueous film forming foam (AFFF); Stormwater; Silica-based granular nedia (SGM); Nucleophile; Photocatalysis; Advanced oxidation

Funding

  1. US Department of Defense through the Strategic Environmental Research and Development Program (SERDP) [ER19-1403]

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PFASs, especially sulfonates, are challenging to remove using traditional methods. This research demonstrates successful degradation and defluorination of PFOS using a novel photocatalytic SGM activated with UV light, with sodium thiosulfate proving to be the most effective nucleophile. The study suggests potential pathways for PFOS destruction and its application to other contaminants.
Per- and polyfluoroalkyl substances (PFASs) are recalcitrant emerging contaminants of concern within the United States and internationally. Of the known PFASs, the sulfonates are considered among the most toxic and difficult to destroy using traditional methods. Research presented herein describes the degradation and defluorination of perfluorooctane sulfonate (PFOS) using a novel photocatalytic porous silicabased granular media (SGM) activated with ultraviolet light, and combined with a strong or weak nucleophilic attack in batch reactors. Sodium thiosulfate proved to be the most compatible and efficient nucleophile in combination with SGM media production of free radicals. Measured aqueous fluoride content accounted for 51% defluorination of PFOS, while the remainder is theorized to mineralize and reside within the porous network of the SGM, as indicated by scanning electron microscopy and energy dispersive x-ray spectroscopy. Removal of PFOS in solution is completed by 30 min with Na2S2O3, with measurable by-product production of C2F3O2- and aqueous fluoride occurring at 15 min. The rapid increase, incipient decrease, and subsequent mineralization of fluoride reveals that the degradation of PFOS is rapid and starts with cleaving of the functional sulfonate group. Amalgamated C-F chains precipitate within the SGM alongside the crystalized fluorine. Possible pathways for PFOS destruction are proposed for the combined attack results. This approach is translatable to other PFASs and organic contaminants of concern. (C) 2021 American Society of Civil Engineers.

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