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    Field Demonstration of a Sonolysis Reactor for Treatment of PFAS-Contaminated Groundwater

    Source: Journal of Environmental Engineering:;2022:;Volume ( 148 ):;issue: 011::page 06022005
    Author:
    Poonam R. Kulkarni
    ,
    Stephen D. Richardson
    ,
    Blossom N. Nzeribe
    ,
    David T. Adamson
    ,
    Shashank S. Kalra
    ,
    Shaily Mahendra
    ,
    Jens Blotevogel
    ,
    Andrea Hanson
    ,
    Greg Dooley
    ,
    Sharyl Maraviov
    ,
    Jovan Popovic
    DOI: 10.1061/(ASCE)EE.1943-7870.0002064
    Publisher: ASCE
    Abstract: A 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.
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      Field Demonstration of a Sonolysis Reactor for Treatment of PFAS-Contaminated Groundwater

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    http://yetl.yabesh.ir/yetl1/handle/yetl/4287587
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    • Journal of Environmental Engineering

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    contributor authorPoonam R. Kulkarni
    contributor authorStephen D. Richardson
    contributor authorBlossom N. Nzeribe
    contributor authorDavid T. Adamson
    contributor authorShashank S. Kalra
    contributor authorShaily Mahendra
    contributor authorJens Blotevogel
    contributor authorAndrea Hanson
    contributor authorGreg Dooley
    contributor authorSharyl Maraviov
    contributor authorJovan Popovic
    date accessioned2022-12-27T20:34:02Z
    date available2022-12-27T20:34:02Z
    date issued2022/11/01
    identifier other(ASCE)EE.1943-7870.0002064.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4287587
    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.
    publisherASCE
    titleField Demonstration of a Sonolysis Reactor for Treatment of PFAS-Contaminated Groundwater
    typeJournal Article
    journal volume148
    journal issue11
    journal titleJournal of Environmental Engineering
    identifier doi10.1061/(ASCE)EE.1943-7870.0002064
    journal fristpage06022005
    journal lastpage06022005_12
    page12
    treeJournal of Environmental Engineering:;2022:;Volume ( 148 ):;issue: 011
    contenttypeFulltext
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