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Evaluation of transformation products from chemical oxidation of micropollutants in wastewater by photoassisted generation of sulfate radicals

机译:光辅助产生硫酸根对废水中微量污染物化学氧化转化产物的评价

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摘要

In this research, the degradation of seven different micropollutants (MPs) and the formation of their transformation products (TPs) have been assessed during the application of different advanced oxidation processes: photolytic and photocatalytic activation of peroxymonosulfate (PMS) and persulfate (PS). The results were compared with those obtained from the photolytic experiments using hydrogen peroxide (H2O2) as oxidant. A significant abatement of almost all MPs was achieved, even with very low UV-C contact time (9 and 28 s). The degradation of atenolol (ATN) and caffeine (CFN) ranged from 84 to 100% with a dose of 0.5 mM of any oxidant. The efficiencies for bisphenol-A (BPA), carbamazepine (CBZ), diclofenac (DCF), ibuprofen (IBP), and sulfamethoxazole (SMX) varied depending on the oxidation system and operating conditions (oxidant dose and UV-C contact time), leading to the photolysis of PMS to higher efficiencies than PS and H2O2. In all cases, the abatement of MPs ranged from 63 to 83%, even with the lowest PMS dosage. Moreover, the addition of Fe(II) as a catalyst enhanced the removal efficiency, reaching almost total removal, especially over CBZ, DCF, and IBP. The Dissolved Organic Carbon (DOC) removal ranged between 44 and 62%, suggesting the transformation of MPs in intermediate compounds. The identification of transformation products was carried out for each micropollutant and each oxidation treatment, being observed some transformation products specific of oxidation by sulfate radicals. For example, m/z 165.0432 only appeared after PMS/Fe(II)/W-C on the degradation of BFA, m/z 251.082 appeared after photolytic activation of PMS and PS on CBZ removal, and m/z 128.0452 was observed after any sulfate radical oxidation treatment, but not after photolysis of H2O2. (C) 2019 Elsevier Ltd. All rights reserved.
机译:在这项研究中,已在应用不同的高级氧化过程期间评估了七种不同的微污染物(MPs)的降解及其转化产物(TPs)的形成:过氧单硫酸盐(PMS)和过硫酸盐(PS)的光催化和光催化活化。将结果与使用过氧化氢(H2O2)作为氧化剂的光解实验获得的结果进行了比较。即使UV-C的接触时间很短(9和28 s),也几乎可以消除所有MP。剂量为0.5 mM的任何氧化剂,阿替洛尔(ATN)和咖啡因(CFN)的降解范围为84%至100%。双酚A(BPA),卡马西平(CBZ),双氯芬酸(DCF),布洛芬(IBP)和磺胺甲恶唑(SMX)的效率因氧化系统和操作条件(氧化剂剂量和UV-C接触时间)而异,导致PMS的光解效率高于PS和H2O2。在所有情况下,即使使用最低的PMS剂量,MP的减少范围也从63%到83%。此外,添加Fe(II)作为催化剂可提高去除效率,几乎达到完全去除效果,尤其是在CBZ,DCF和IBP上。溶解有机碳(DOC)的去除率介于44%和62%之间,表明MP在中间化合物中的转化。对每种微量污染物和每种氧化处理进行转化产物的鉴定,观察到一些硫酸根自由基特有的氧化转化产物。例如,仅在PMS / Fe(II)/ WC降解BFA之后才出现m / z 165.0432,在去除CBZ的PMS和PS进行光解活化后才出现m / z 251.082,而在任何硫酸盐处理后观察到m / z 128.0452自由基氧化处理,但不能在H2O2光解后进行。 (C)2019 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Chemosphere》 |2019年第7期|509-519|共11页
  • 作者单位

    Univ Rey Juan Carlos, Dept Chem & Environm Technol ESCET, C Tulipan S-N, Madrid 28933, Spain|Univ Politecn Madrid, Escuela Tecn Super Ingn Ind, Dept Ind Chem & Environm Engn, C Jose Gutierrez Abascal 2, E-28006 Madrid, Spain;

    Univ Rey Juan Carlos, Dept Chem & Environm Technol ESCET, C Tulipan S-N, Madrid 28933, Spain;

    Univ Torino, Dept Chem, Via P Giuria 5, I-10125 Turin, Italy;

    FCC Aqualia SA, Dept Innovat & Technol, C Montesinos 28, Badajoz 06002, Spain;

    Univ Torino, Dept Mol Biotechnol & Hlth Sci, Via Nizza 52, I-10125 Turin, Italy;

    Univ Torino, Dept Chem, Via P Giuria 5, I-10125 Turin, Italy;

    Univ Torino, Dept Chem, Via P Giuria 5, I-10125 Turin, Italy;

    Univ Rey Juan Carlos, Dept Chem & Environm Technol ESCET, C Tulipan S-N, Madrid 28933, Spain;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Sulfate radicals; Micropollutants; Transformation products; Mechanisms; UV-C radiation;

    机译:硫酸根;微污染物;转化产物;机理;UV-C辐射;

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