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Chloramination of nitrogenous contaminants (Pharmaceuticals and pesticides): NDMA and halogenated DBPs formation

机译:含氮污染物(药物和农药)的氯化:NDMA和卤化DBP的形成

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摘要

Disinfection with chloramines is often used to reduce the production of regulated disinfection by-products (DBPs) such as trihalomethanes (THMs) and haloacetic acids (HAAs). However, chloramination can lead to the formation of N-nitrosamines, including N-nitrosodimethylamine (NDMA), a probable human carcinogen. Previous research used dimethylamine (DMA) as a model precursor of NDMA, but certain widely used tertiary dimethylamines (e.g. the pharmaceutical ranitidine) show much higher conversion rates to NDMA than DMA. This study investigates the NDMA formation potential of several tertiary amines including Pharmaceuticals and herbicides. The reactivity of these molecules with monochloramine (NH_2C1) is studied through the formation of NDMA, and other halogenated DBPs such as haloacetonitriles (HANs) and AOX (Adsorbable Organic Halides). Several compounds investigated formed NDMA in greater amounts than DMA, revealing the importance of structural characteristics of tertiary amines for NDMA formation. Among these compounds, the pharmaceutical ranitidine showed the highest molar conversion to NDMA. The pH and dissolved oxygen content of the solution were found to play a major role for the formation of NDMA from ranitidine. NDMA was formed in higher amounts at pH around pH 8 and a lower concentration of dissolved oxygen dramatically decreased NDMA yields. These findings seem to indicate that dichloramine (NHC12) is not the major oxidant involved in the formation of NDMA from ranitidine, results in contradiction with the reaction mechanisms proposed in the literature. Dissolved oxygen was also found to influence the formation of other oxygen-containing DBPs (i.e. tri-chloronitromethane and haloketones). The results of this study identify several anthropogenic precursors of NDMA, indicating that chloramination of waters impacted by these tertiary amines could lead to the formation of significant amounts of NDMA and other non-regulated DBPs of potential health concern (e.g. dichloroacetonitrile or trichloronitro-methane). This could be of particular importance for the chloramination of wastewater effluents, especially during water reuse processes.
机译:通常使用氯胺消毒来减少受控消毒副产物(DBP)的产生,例如三卤甲烷(THMs)和卤乙酸(HAA)。但是,氯化会导致N-亚硝胺的形成,包括N-亚硝基二甲胺(NDMA),一种可能的人类致癌物。先前的研究使用二甲基胺(DMA)作为NDMA的模型前体,但是某些广泛使用的叔二甲基胺(例如药物雷尼替丁)显示出比DMA高得多的NDMA转化率。这项研究调查了包括药物和除草剂在内的几种叔胺的NDMA形成潜力。通过形成NDMA和其他卤代DBP(例如卤代乙腈(HANs)和AOX(可吸附有机卤化物)),研究了这些分子与一氯胺(NH_2C1)的反应性。研究的几种化合物形成的NDMA的数量比DMA的数量大,这表明叔胺的结构特征对于NDMA形成的重要性。在这些化合物中,药物雷尼替丁显示出最高的向NDMA的摩尔转化率。发现溶液的pH和溶解氧含量对于由雷尼替丁形成NDMA起主要作用。 NDMA在pH值约为8时以较高的量形成,而较低的溶解氧浓度会大大降低NDMA的产量。这些发现似乎表明,二氯胺(NHC12)不是从雷尼替丁形成NDMA的主要氧化剂,与文献中提出的反应机理相矛盾。还发现溶解氧会影响其他含氧DBP(即三氯硝基甲烷和卤代酮)的形成。这项研究的结果确定了NDMA的几种人为前体,这表明受这些叔胺影响的水被氯化会导致大量NDMA的形成和其他潜在的健康隐患(例如二氯乙腈或三氯硝基甲烷)。 。这对于废水废水的氯化特别重要,尤其是在水回用过程中。

著录项

  • 来源
    《Water Research》 |2011年第10期|p.3164-3174|共11页
  • 作者单位

    Laboratoire de Chimie et Microbiologie de VEau (CNRS UMR 6008), Universite de Poitiers - ENSIP, 40 Avenue du Recteur Pineau,86022 Poitiers Cedex, France;

    Laboratoire de Chimie et Microbiologie de VEau (CNRS UMR 6008), Universite de Poitiers - ENSIP, 40 Avenue du Recteur Pineau,86022 Poitiers Cedex, France;

    Laboratoire de Chimie et Microbiologie de VEau (CNRS UMR 6008), Universite de Poitiers - ENSIP, 40 Avenue du Recteur Pineau,86022 Poitiers Cedex, France;

  • 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

    ndma; nitrosamine; chloramination; disinfection by-products; ranitidine;

    机译:恩达;亚硝胺;氯化;消毒副产物;雷尼替丁;
  • 入库时间 2022-08-17 13:48:26

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