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dc.contributor.authorPoonam R. Kulkarni
dc.contributor.authorStephen D. Richardson
dc.contributor.authorBlossom N. Nzeribe
dc.contributor.authorDavid T. Adamson
dc.contributor.authorShashank S. Kalra
dc.contributor.authorShaily Mahendra
dc.contributor.authorJens Blotevogel
dc.contributor.authorAndrea Hanson
dc.contributor.authorGreg Dooley
dc.contributor.authorSharyl Maraviov
dc.contributor.authorJovan Popovic
dc.date.accessioned2022-12-27T20:34:02Z
dc.date.available2022-12-27T20:34:02Z
dc.date.issued2022/11/01
dc.identifier.other(ASCE)EE.1943-7870.0002064.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4287587
dc.description.abstractA mobile treatment system equipped with a custom-built sonolysis reactor was deployed at a site in California to treat groundwater impacted with per- and polyfluoroalkyl substances (PFAS). Extracted groundwater was treated in a 700-kHz sonolysis reactor for batch treatment under different power densities (122, 203, and 305  W/L) and operating temperatures (15°C and 25°C). Sonolytic treatment resulted in 93%–100% removal of the 15 PFAS identified in the groundwater, and PFAS degradation rates increased proportionally with increasing power density and temperature at operating conditions of 25°C. For all experimental conditions evaluated, greater removal was observed for perfluorinated carboxylic acids (PFCAs) [e.g., 95.1% to 100% for perfluorohexanoic acid (PFHxA)] than perfluorinated sulfonic acids (PFSAs) [68.3% to 95.2% for perfluorohexane sulfonate (PFHxS)] for similar carbon chain lengths. Similarly, greater removal was observed for longer-chain PFAS [e.g., 95.4% to 99.5% for perfluorooctanoic acid (PFOA)] compared with short-chain PFAS [56.9% to 90.4% for perfluorobutanoic acid (PFBA)]. Substantial removal of total oxidizable precursors (TOP) and specific precursors [65.5% to 99.1% for 4:2 fluorotelomer sulfonate (FTS), 6:2 FTS, 8:2 FTS, and perfluorooctane sulfonamide (FOSA)] was also observed under all conditions tested. Additionally, formation of nitrate was observed, with concentrations below maximum contaminant levels (MCLs). Overall, the results demonstrate that sonolysis treatment of PFAS-contaminated groundwater can effectively degrade PFAS without the formation of short-chain PFAS and the oxidation byproducts chlorate and perchlorate.
dc.publisherASCE
dc.titleField Demonstration of a Sonolysis Reactor for Treatment of PFAS-Contaminated Groundwater
dc.typeJournal Article
dc.journal.volume148
dc.journal.issue11
dc.journal.titleJournal of Environmental Engineering
dc.identifier.doi10.1061/(ASCE)EE.1943-7870.0002064
dc.journal.fristpage06022005
dc.journal.lastpage06022005_12
dc.page12
dc.treeJournal of Environmental Engineering:;2022:;Volume ( 148 ):;issue: 011
dc.contenttypeFulltext


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