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Molecular characteristics of dissolved organic matter transformed by O_3 and O_3/H_2O_2 treatments and the effects on formation of unknown disinfection by-products

机译:O_3和O_3 / H_2O_2治疗转化的溶解有机物的分子特性及对未知消毒副产品的影响

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摘要

We investigated semiquantitative changes in almost 1000 dissolved organic matter (DOM) features during oxidation with 1 mg of O-3 per liter (mg OA), 4 mg O-3/L, or 4 mg O-3/L + 2.5 mg of H2O2 per liter (advanced oxidation process, AOP) by unknown screening analysis with Orbitrap mass spectrometry. The consequential effects on formation of unknown disinfection by-products (DBPs) by chlorination were evaluated in laboratory-scale experiments. Several hundred unsaturated DOM features with positive oxygen-subtracted double bond equivalents per carbon ((DBE-O)/C) were decomposed by the ozone only treatment and AOP. The AOP decomposed some saturated (negative (DBE-O)/C)) and reduced molecules, which had negative carbon oxidation states (C-os). Several hundred saturated oxidation by-products were detected after ozonation and the AOP. After chlorination, the samples pre-treated with ozone alone resulted in higher formation of unknown DBPs than the AOP pre-treated sample or the sample without oxidation. Over half of the DBP precursors, estimated by electrophilic substitution, were not totally decomposed by any oxidation process, but they were increased after the ozone-only process and AOR DBP precursors produced by the ozone-only process or AOP formed unique unknown DBPs. Therefore, post-treatment processes after oxidation and before chlorination are important to minimize formation of unknown DBPs. (C) 2019 Elsevier Ltd. All rights reserved.
机译:在氧化过程中,我们研究了几乎1000次溶解有机物(DOM)特征的半定量变化,每升1mg O-3(Mg OA),4mg O-3 / L或4mg O-3 / L + 2.5mg H2O2每升(晚期氧化过程,AOP)通过露珠质谱法未知筛选分析。在实验室规模实验中评估了通过氯化形成未知消毒副产物(DBPS)的相应影响。几百个不饱和DOM特征具有每种碳((DBE-O)/ c)的正氧减去双键当量的氧化碳((DBE-O)/ c)分解,仅由臭氧处理和AOP分解。 AOP分解一些饱和(负(DBE-O)/ c))和还原的分子,其具有负碳氧化态(C-OS)。在臭氧和AOP之后检测到几百饱和氧化副产物。氯化后,单独用臭氧预处理的样品比AOP预处理的样品或样品更高地形成未知的DBP或没有氧化的样品。通过亲电子取代估计的DBP前体的一半以上估计并不完全通过任何氧化过程分解,但在唯一的过程和由臭氧过程或AOP产生的AOR DBP前体之后,它们增加了独特的未知Dbps。因此,氧化后和氯化前的后处理过程对于最小化未知Dbps的形成是重要的。 (c)2019 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Water Research》 |2019年第1期|214-222|共9页
  • 作者单位

    Univ Tokyo Sch Engn Res Ctr Water Environm Technol Bunkyo Ku 7-3-1 Hongo Tokyo 1138656 Japan|Khon Kaen Univ Fac Engn Dept Environm Engn Khon Kaen 40002 Thailand|Khon Kaen Univ Res Ctr Environm & Hazardous Subst Management Khon Kaen 40002 Thailand|Chulalongkorn Univ Ctr Excellence Hazardous Subst Management HSM Bangkok 10330 Thailand;

    Univ Tokyo Sch Engn Res Ctr Water Environm Technol Bunkyo Ku 7-3-1 Hongo Tokyo 1138656 Japan;

    Univ Tokyo Sch Engn Dept Urban Engn Bunkyo Ku 7-3-1 Hongo Tokyo 1138656 Japan;

    Univ Tokyo Sch Engn Res Ctr Water Environm Technol Bunkyo Ku 7-3-1 Hongo Tokyo 1138656 Japan;

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

    Advanced water treatment; Dissolved organic matter; Orbitrap mass spectrometry; Unknown disinfection by-product; Unknown screening analysis;

    机译:高级水处理;溶解有机物;orbitrap质谱;未知消毒副产品;未知的筛选分析;

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