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dc.contributor.authorLe Roux, J.
dc.contributor.authorGallard, H.
dc.contributor.authorCroué, Jean-Philippe
dc.date.accessioned2017-03-15T22:16:40Z
dc.date.available2017-03-15T22:16:40Z
dc.date.created2017-02-26T19:31:40Z
dc.date.issued2011
dc.identifier.citationLe 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.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/49865
dc.identifier.doi10.1016/j.watres.2011.03.035
dc.description.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.

dc.publisherIWA Publishing
dc.titleChloramination of nitrogenous contaminants (pharmaceuticals and pesticides): NDMA and halogenated DBPs formation
dc.typeJournal Article
dcterms.source.volume45
dcterms.source.number10
dcterms.source.startPage3164
dcterms.source.endPage3174
dcterms.source.issn0043-1354
dcterms.source.titleWater Research
curtin.departmentCurtin Water Quality Research Centre
curtin.accessStatusFulltext not available


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