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The increasing global water demand has prompted the reuse of treated wastewater. However, the persistence of organic micropollutants in inefficiently treated effluents can have detrimental effects depending on the scope of the reclaimed water usage. One example is the presence of sulfamethoxazole, a widely used antibiotic whose interference with the folate synthesis pathway negatively affects plants and microorganisms. The goal of this study is to assess the suitability of a non-thermal plasma-ozonation technique for the removal of the organic pollutant and reduction of its herbicidal effect. Fast sulfamethoxazole degradation was achieved with apparent reaction rate constants in the range 0.21-0.49 min -1 , depending on the initial concentration. The highest energy yield (64.5 g/kWh at 50 % removal) exceeds the values reported thus far in plasma degradation experiments. During treatment, 38 degradation intermediates were detected and identified, of which only 9 are still present after 60 min. The main reactive species that contribute to the degradation of sulfamethoxazole and its intermediate products were hydroxyl radicals and ozone, which led to the formation of several hydroxylated compounds, ring opening and fragmentation. The herbicidal effect of the target compound was eliminated with its removal, showing that the remanent intermediates do not retain phytotoxic properties., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier B.V.)

A pulsed corona discharge above liquid combined with ozonation has been investigated for the degradation of organic pollutants in water, as well as regarding the generation of several oxidizing species: ozone in gas phase, hydrogen peroxide and hydroxyl radicals in the liquid. A considerable improvement in the energy efficiency for organic compounds removal has been observed when reducing the width of the discharge pulses. This finding was correlated with the efficient formation of oxidizing species in case of short pulses. Recycling of the effluent gas from the plasma also enhances contaminants degradation. This was mainly attributed to an in situ peroxone process, i.e. the reaction between plasma-generated O 3 and H 2 O 2 , forming highly reactive OH radicals, largely responsible for organic compounds degradation. This assumption is supported by the decline in O 3 and H 2 O 2 concentrations and simultaneous increase in OH concentration detected in plasma-ozonation experiments as compared to results obtained with plasma alone., (Copyright © 2019 Elsevier Ltd. All rights reserved.)

The degradation of methylparaben (MeP) in water was investigated using a pulsed corona discharge generated in oxygen, above the liquid. A comparison was made between results obtained in semi-batch corona (SBC) configuration (stationary solution, continuous gas flow) and results obtained in a semi-batch corona with recirculation combined with ozonation (SBCR + O3), where the liquid is continuously circulated between a solution reservoir and the plasma reactor and the effluent gas containing ozone is bubbled through the solution in the reservoir. It was found that MeP was completely degraded after 10-15 min of treatment in both configurations. Oxidation by ozone alone, in the absence of plasma, was a slower process. The energy efficiency for MeP removal (Y MeP) and for mineralization (Y TOC) was significantly higher in the SBCR + O3 configuration (Y MeP = 7.1 g/kWh at 90 % MeP removal and Y TOC = 0.41 g/kWh at 50 % total organic carbon (TOC) removal) than in the SBC configuration (Y MeP = 0.6 g/kWh at 90 % MeP removal and Y TOC = 0.11 g/kWh at 50 % TOC removal).

The objective of these investigations is to understand in more detail how organic compounds in water are degraded during plasma treatment. The formation of oxidizing species (ozone (O 3 ), hydrogen peroxide (H 2 O 2 ) and hydroxyl radicals ( OH)) in a pulsed corona discharge in contact with liquid is investigated. The degradation of a target organic compound (methylparaben) in aqueous solution was increased when combining plasma treatment with ozonation, using the O 3 generated in the discharge. Enhanced mass transfer of O 3 obtained in this plasma+O 3 configuration leads to a six fold increase of MeP oxidation rate. The evolution of oxidants concentration during treatment of MeP solutions provides information on their consumption in reactions with MeP and its oxidation products. The correlation of MeP degradation results (MeP removal and mineralization) with O 3 consumption and the identified reaction products confirms that although O 3 plays an important role in the degradation, for the mineralization OH radicals have an essential contribution. The concentration of OH radicals is diminished in the solutions containing MeP as compared to plasma-treated water, indicating OH consumption in reactions with the target compound and its degradation products. The concentration of H 2 O 2 in the liquid can be either increased or reduced in the presence of MeP, depending on its initial concentration. On the one hand, decomposition of H 2 O 2 by OH or O 3 is suppressed in the presence of MeP, but on the other hand less OH radicals are available for its formation. [ABSTRACT FROM AUTHOR]