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dc.contributor.authorAkshay Chandrashekar Parenky
dc.contributor.authorNaomi Gevaerd de Souza
dc.contributor.authorHiep H. Nguyen
dc.contributor.authorJunha Jeon
dc.contributor.authorHyeok Choi
dc.date.accessioned2022-01-30T21:35:56Z
dc.date.available2022-01-30T21:35:56Z
dc.date.issued10/1/2020 12:00:00 AM
dc.identifier.other%28ASCE%29EE.1943-7870.0001808.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4268501
dc.description.abstractPerfluoroalkyl and polyfluoroalkyl substances (PFAS), widely used in many commercial and military products, have been notorious due to their environmental persistence. Even radical-based advanced oxidation technologies have been reported to be less effective for decomposition of PFAS, particularly perfluoroalkyl ones, while commonly requiring energy-intensive extreme conditions and tools such as ultraviolet, ultrasound, microwave, electron beam, and high temperatures. Herein, for the first time, the potential of a modified Fenton system, i.e., homogeneous persulfate (PS) conjugated with silver (Ag+), to decompose PFAS under ambient conditions is communicated. Among many combinations of common oxidants and transition metals tested, only the PS/Ag pair showed significant reactivity at 20°C exclusively toward carboxylic PFAS including perfluorooctanoic acid, resulting in evolution of fluoride ion release and reaction by-product formation. Although sulfonic PFAS still remain challenging, and follow-up assignments are raised to investigate in-depth mechanisms and examine other oxidant and metal pairs, this study offers one step closer to establishing an energy-independent and more practical treatment system for PFAS.
dc.publisherASCE
dc.titleDecomposition of Carboxylic PFAS by Persulfate Activated by Silver under Ambient Conditions
dc.typeJournal Paper
dc.journal.volume146
dc.journal.issue10
dc.journal.titleJournal of Environmental Engineering
dc.identifier.doi10.1061/(ASCE)EE.1943-7870.0001808
dc.page6
dc.treeJournal of Environmental Engineering:;2020:;Volume ( 146 ):;issue: 010
dc.contenttypeFulltext


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