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

机译:硫酸盐自由基废水中微污染物的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:在该研究中,在应用不同的晚期氧化过程期间,已经评估了七种不同微舒适剂(MPS)的降解和其转化产物(TPS)的形成:过氧键硫酸盐(PMS)和过硫酸盐(PS)的光解和光催化活化。将结果与使用过氧化氢(H 2 O 2)作为氧化剂的光解实验获得的结果。即使具有非常低的UV-C接触时间(9和28秒),也实现了几乎所有MP的显着减少。阿绿龙(ATN)和咖啡因(CFN)的降解范围为84至100%,剂量为0.5mm的任何氧化剂。双酚-A(BPA),卡巴马啶(CBZ),双氯芬酸(DCF),布洛芬(IBP)和磺胺甲恶唑(SMX)的效率根据氧化系统和操作条件(氧化剂剂量和UV-C接触时间)而变化,导致PM的光解至比PS和H2O2更高的效率。在所有情况下,即使具有最低PMS剂量,MPS的削减量范围为63至83%。此外,添加Fe(II)作为催化剂增强了去除效率,几乎达到了总除去,特别是在CBZ,DCF和IBP上。去除溶解的有机碳(DOC)的去除率在44至62%之间,表明中间体化合物中的MPS转化。对每种微量舒适剂和每种氧化处理进行转化产物的鉴定,观察到一些硫酸盐自由基氧化的转化产物。例如,在PMS / Fe(II)/ Wc上仅出现在BFA的降解后的M / Z 165.0432,在CBZ去除PMS和PS的PMS和PS对CBZ去除后出现的M / Z 251.082,在任何硫酸盐后观察到M / Z 128.0452自由基氧化处理,但在H2O2的光解后没有。 (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:硫酸盐基团;微核性;转型产品;机制;UV-C辐射;

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