Curtin University Homepage
  • Library
  • Help
    • Admin

    espace - Curtin’s institutional repository

    JavaScript is disabled for your browser. Some features of this site may not work without it.
    View Item 
    • espace Home
    • espace
    • Curtin Research Publications
    • View Item
    • espace Home
    • espace
    • Curtin Research Publications
    • View Item

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

    Access Status
    Fulltext not available
    Authors
    Le Roux, J.
    Gallard, H.
    Croué, Jean-Philippe
    Date
    2011
    Type
    Journal Article
    
    Metadata
    Show full item record
    Citation
    Le Roux, J. and Gallard, H. and Croué, J. 2011. Chloramination of nitrogenous contaminants (pharmaceuticals and pesticides): NDMA and halogenated DBPs formation. Water Research. 45 (10): pp. 3164-3174.
    Source Title
    Water Research
    DOI
    10.1016/j.watres.2011.03.035
    ISSN
    0043-1354
    School
    Curtin Water Quality Research Centre
    URI
    http://hdl.handle.net/20.500.11937/49865
    Collection
    • Curtin Research Publications
    Abstract

    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 (NH2Cl) 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 (NHCl2) 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. trichloronitromethane 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 trichloronitromethane). This could be of particular importance for the chloramination of wastewater effluents, especially during water reuse processes.

    Related items

    Showing items related by title, author, creator and subject.

    • Formation of NDMA by chloramination of nitrogenous contaminants: Potential role of bromide and dissolved oxygen
      Le Roux, J.; Gallard, H.; Croue, Jean-Philippe (2011)
      Disinfection with monochloramine is known to significantly reduce the formation of regulated disinfection by-products (i.e. trihalomethanes and haloacetic acids) as compared to chlorination. Moreover, monochloramine can ...
    • NDMA formation mechanism by chloramination of tertiary amines
      Le Roux, J.; Gallard, H.; Croue, Jean-Philippe; Papot, S.; Deborde, M. (2012)
      Chloramination is used to reduce the formation of regulated disinfection by-products (i.e. trihalomethanes and haloacetic acids), or to avoid biofouling of membranes during wastewater reclamation processes. However, ...
    • NDMA formation by chloramination of ranitidine: Kinetics and mechanism
      Roux, J.; Gallard, H.; Croué, Jean-Philippe; Papot, S.; Deborde, M. (2012)
      The kinetics of decomposition of the pharmaceutical ranitidine (a major precursor of NDMA) during chloramination was investigated and some decomposition byproducts were identified by using high performance liquid ...
    Advanced search

    Browse

    Communities & CollectionsIssue DateAuthorTitleSubjectDocument TypeThis CollectionIssue DateAuthorTitleSubjectDocument Type

    My Account

    Admin

    Statistics

    Most Popular ItemsStatistics by CountryMost Popular Authors

    Follow Curtin

    • 
    • 
    • 
    • 
    • 

    CRICOS Provider Code: 00301JABN: 99 143 842 569TEQSA: PRV12158

    Copyright | Disclaimer | Privacy statement | Accessibility

    Curtin would like to pay respect to the Aboriginal and Torres Strait Islander members of our community by acknowledging the traditional owners of the land on which the Perth campus is located, the Whadjuk people of the Nyungar Nation; and on our Kalgoorlie campus, the Wongutha people of the North-Eastern Goldfields.