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Comparative study on 2,4-dichlorophenoxyacetic acid and 2,4-dichlorophenol removal from aqueous solutions via ozonation, photocatalysis and non-thermal plasma using a planar falling film reactor
[Display omitted] •Ozonation, photocatalysis and non-thermal DBD plasma were compared.•Enhanced energy yield observed by combination of Fenton with non-thermal plasma.•Photocatalytic ozonation provides highest TOC removal.•Degradation of by-products formed during 2,4-D decomposition were examined.•O...
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Published in: | Journal of hazardous materials 2018-02, Vol.343, p.107-115 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Ozonation, photocatalysis and non-thermal DBD plasma were compared.•Enhanced energy yield observed by combination of Fenton with non-thermal plasma.•Photocatalytic ozonation provides highest TOC removal.•Degradation of by-products formed during 2,4-D decomposition were examined.•Oxidation by DBD was influenced by the nature of gas composition.
Ozonation and advanced oxidation processes based on photocatalysis (P.C.) and non-thermal plasma generated in a dielectric barrier discharge (DBD) in different gas atmospheres were compared for the degradation and mineralization of 2,4-dichlorophenoxy acetic acid (2,4-D) and 2,4-dichlorophenol (2,4-DCP) in aqueous solutions, using a planar falling film reactor with comparable design. The energetic yields (G50) as measure of the efficiencies of the different methods are for 2,4-D in the order DBD/Ar-Fenton>ozonation>DBD/Ar>P.C.ozonation>DBD/Ar:O2≫DBD/Air>P.C.oxidation. For 2,4-DCP the order is ozonation≫DBD/Ar-Fenton>P.C.ozonation>DBD/Ar>DBD/Ar:O2≫P.C.oxidation>DBD/Air. The degradation by using ozone is very effective, but it should be noted that the mineralization measured by the total organic carbon (TOC) removal is low. The reason is the formation of stable towards ozone intermediates, especially low chain carboxylic acids. The fate of these intermediates during the degradation with the different methods has been followed and discussed. |
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ISSN: | 0304-3894 1873-3336 |
DOI: | 10.1016/j.jhazmat.2017.09.025 |