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与液体接触的电晕放电中氧化物种的形成及其与有机化合物反应的新证据。

New evidence on the formation of oxidizing species in corona discharge in contact with liquid and their reactions with organic compounds.

作者信息

Magureanu M, Dobrin D, Bradu C, Gherendi F, Mandache N B, Parvulescu V I

机构信息

National Institute for Lasers, Plasma and Radiation Physics, Department of Plasma Physics and Nuclear Fusion, Atomistilor Str. 409, P.O. Box MG-36, 077125, Magurele, Bucharest, Romania.

National Institute for Lasers, Plasma and Radiation Physics, Department of Plasma Physics and Nuclear Fusion, Atomistilor Str. 409, P.O. Box MG-36, 077125, Magurele, Bucharest, Romania.

出版信息

Chemosphere. 2016 Dec;165:507-514. doi: 10.1016/j.chemosphere.2016.09.073. Epub 2016 Sep 30.

Abstract

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), hydrogen peroxide (HO) 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 generated in the discharge. Enhanced mass transfer of O obtained in this plasma+O 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 consumption and the identified reaction products confirms that although O 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 HO 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 HO by OH or O is suppressed in the presence of MeP, but on the other hand less OH radicals are available for its formation.

摘要

这些研究的目的是更详细地了解水中的有机化合物在等离子体处理过程中是如何降解的。研究了与液体接触的脉冲电晕放电中氧化物种(臭氧(O)、过氧化氢(HO)和羟基自由基(OH))的形成。当将等离子体处理与臭氧化相结合时,利用放电中产生的O,水溶液中目标有机化合物(对羟基苯甲酸甲酯)的降解率提高。在这种等离子体+O配置中获得的O的增强传质导致MeP氧化速率提高了六倍。在处理MeP溶液过程中氧化剂浓度的变化提供了它们在与MeP及其氧化产物反应中消耗情况的信息。MeP降解结果(MeP去除和矿化)与O消耗以及鉴定出的反应产物之间的相关性证实,虽然O在降解中起重要作用,但对于矿化,OH自由基有重要贡献。与经等离子体处理的水相比,含MeP溶液中OH自由基的浓度降低,这表明OH在与目标化合物及其降解产物的反应中被消耗。在MeP存在的情况下,液体中HO的浓度可能会增加或降低,这取决于其初始浓度。一方面,在MeP存在的情况下,OH或O对HO的分解受到抑制,但另一方面,用于其形成的OH自由基较少。

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