AI Article Synopsis

  • PFOA is a harmful chemical that persists in the environment and poses health risks, prompting the need for effective removal methods.
  • A novel gas-liquid dielectric barrier discharge (GLDBD) reactor designed in this study achieved over 98% PFOA removal in different water types within 50 minutes, utilizing reactive species like hydroxyl radicals and reactive nitrogen species to break down the compound.
  • The research highlights the reactor's robustness against various water conditions and proposes effective PFOA degradation pathways, indicating its potential for practical applications in water treatment.

Article Abstract

Perfluorooctanoic acid (PFOA) poses a serious threat to the ecological environment and biological health because of its ubiquitous distribution, extreme persistence, and high toxicity. In this study, we designed a novel gas-liquid dielectric barrier discharge (GLDBD) reactor which could efficiently destruct PFOA. PFOA removal efficiencies can be obtained in various water matrices, which were higher than 98.0% within 50 min, with energy yields higher than 114.5 mg·kWh. It was confirmed that the reactive species including e, ONOOH, •NO, and hydroxyl radicals (•OH) were responsible for PFOA removal. Especially, this study first revealed the crucial role of reactive nitrogen species (RNS) for PFOA degradation in the plasma system. Due to the generation of a large amount of RNS, the designed GLDBD reactor proved to be less sensitive to various water matrices, which meant a broader promising practical application. Moreover, influential factors including high concentration of various ions and humic acid (HA), were investigated. The possible PFOA degradation pathways were proposed based on liquid chromatograph-mass spectrometer (LC-MS) results and density functional theory (DFT) calculation, which further confirmed the feasibility of PFOA removal with RNS. This research, therefore, provides an effective and versatile alternative for PFOA removal from various water matrices.

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Source
http://dx.doi.org/10.1021/acs.est.1c06342DOI Listing

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