Field Demonstration of a Sonolysis Reactor for Treatment of PFAS-Contaminated GroundwaterSource: Journal of Environmental Engineering:;2022:;Volume ( 148 ):;issue: 011::page 06022005Author: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.1943-7870.0002064Publisher: 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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| contributor author | Poonam R. Kulkarni | |
| contributor author | Stephen D. Richardson | |
| contributor author | Blossom N. Nzeribe | |
| contributor author | David T. Adamson | |
| contributor author | Shashank S. Kalra | |
| contributor author | Shaily Mahendra | |
| contributor author | Jens Blotevogel | |
| contributor author | Andrea Hanson | |
| contributor author | Greg Dooley | |
| contributor author | Sharyl Maraviov | |
| contributor author | Jovan Popovic | |
| date accessioned | 2022-12-27T20:34:02Z | |
| date available | 2022-12-27T20:34:02Z | |
| date issued | 2022/11/01 | |
| identifier other | (ASCE)EE.1943-7870.0002064.pdf | |
| identifier uri | http://yetl.yabesh.ir/yetl1/handle/yetl/4287587 | |
| description 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. | |
| publisher | ASCE | |
| title | Field Demonstration of a Sonolysis Reactor for Treatment of PFAS-Contaminated Groundwater | |
| type | Journal Article | |
| journal volume | 148 | |
| journal issue | 11 | |
| journal title | Journal of Environmental Engineering | |
| identifier doi | 10.1061/(ASCE)EE.1943-7870.0002064 | |
| journal fristpage | 06022005 | |
| journal lastpage | 06022005_12 | |
| page | 12 | |
| tree | Journal of Environmental Engineering:;2022:;Volume ( 148 ):;issue: 011 | |
| contenttype | Fulltext |