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Does KMnO4 preoxidation reduce the genotoxicity of disinfection by-products?

机译:KMnO4预氧化是否会降低消毒副产物的遗传毒性?

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摘要

Potassium permanganate (KMnO4) preoxidation is capable of affecting the formation of disinfection by-products (DBPs). However, few studies have focused on the toxicity of DBPs after KMnO4 preoxidation, which is an important index to evaluate alternative treatment processes. Herein genotoxicity (SOS/umu test) was used to clarify the impact of KMnO4 preoxidation on the chlorination byproducts produced from two representative precursors, tyrosine (Tyr) and 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid (BP-4), and their mixture. Results revealed that although KMnO4 could not oxidize BP-4, after chlorination KMnO4 could oxidize the chlorination byproducts of BP-4 and thus decrease the genotoxicity production. For Tyr, KMnO4 preoxidation could increase or decrease the genotoxicity of DBPs, depending on the KMnO4 dose. The optimal initial molar ratio of KMnO4 to Tyr was confirmed to be 1:1. It has been proved that both the oxidation of Tyr by KMnO4 and manganese dioxide (MnO2, the reduction product of KMnO4) and the oxidation of chlorination byproducts by MnO2 can decrease the genotoxicity production of chlorinated Tyr. Remarkably, during chlorination, the competition of manganese(II) oxidation with organic oxidation can result in less chlorine reacting with organics, to induce an increase in genotoxicity. This is the main cause for the increase in genotoxicity of chlorinated Tyr after KMnO4 preoxidation. Additionally, the genotoxicity of the chlorinated mixture was shifted from being higher than the sum of individual genotoxicities of the chlorinated precursors to being lower than their sum with increasing KMnO4 dosage, due to the combined effects between the preoxidation-chlorination products from the two compounds. (C) 2016 Elsevier Ltd. All rights reserved.
机译:高锰酸钾(KMnO4)预氧化能够影响消毒副产物(DBP)的形成。但是,很少有研究集中于KMnO4预氧化后DBP的毒性,这是评估替代处理工艺的重要指标。本文使用遗传毒性(SOS / umu测试)来阐明KMnO4预氧化对由两种代表性前体酪氨酸(Tyr)和2-羟基-4-甲氧基二苯甲酮-5-磺酸(BP-4)产生的氯化副产物的影响,及其混合物。结果表明,尽管KMnO4不能氧化BP-4,但氯化后KMnO4可以氧化BP-4的氯化副产物,从而降低了遗传毒性产生。对于Tyr,KMnO4预氧化可增加或降低DBP的遗传毒性,具体取决于KMnO4剂量。确认KMnO4与Tyr的最佳初始摩尔比为1:1。业已证明,KMnO4和二氧化锰(MnO2,KMnO4的还原产物)对Tyr的氧化和MnO2对氯化副产物的氧化均可降低氯化Tyr的遗传毒性。值得注意的是,在氯化过程中,锰(II)氧化与有机氧化的竞争可导致较少的氯与有机物发生反应,从而引起遗传毒性的增加。这是KMnO4预氧化后氯化Tyr遗传毒性增加的主要原因。另外,由于两种化合物的预氧化氯化产物之间的综合作用,氯化混合物的遗传毒性从高于氯化前体的个别遗传毒性的总和转变为低于其随添加的KMnO4剂量的总遗传毒性的总和。 (C)2016 Elsevier Ltd.保留所有权利。

著录项

  • 来源
    《Chemosphere》 |2016年第11期|73-80|共8页
  • 作者单位

    Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Key Lab Drinking Water Sci & Technol, Beijing 100085, Peoples R China|Univ Chinese Acad Sci, Beijing 100049, Peoples R China;

    Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Key Lab Drinking Water Sci & Technol, Beijing 100085, Peoples R China;

    Chinese Acad Sci, Res Ctr Ecoenvironm Sci, Key Lab Drinking Water Sci & Technol, Beijing 100085, Peoples R China;

  • 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

    Potassium permanganate; Chlorination; DBPs; Genotoxicity; Tyrosine; BP-4;

    机译:高锰酸钾;氯化;DBPs;遗传毒性;酪氨酸;BP-4;

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