Many disinfection by-products (DBPs) are formed during water chlorination, including trihalomethanes (THMs) and haloacetic acids (HAAs). Disinfection with chloramines is often used to reduce the production of regulated DBPs. However, chloramination can lead to the formation of N–nitrosamines, including N–nitrosodimethylamine (NDMA), a probable human carcinogen. The formation mechanisms of NDMA are not fully understood. Proposed mechanisms used dimethylamine (DMA) as a model precursor, but results show that certain widely used tertiary dimethylamines (e.g. the pharmaceutical ranitidine) show much higher conversion rates to NDMA than DMA. These amounts of NDMA cannot be explained by current proposed mechanisms. New formation mechanisms have to be proposed to explain the importance of structural characteristics of tertiary amines for NDMA formation.
Research Article|December 01 2010
Formation of NDMA by Chloramination of Nitrogenous Pharmaceuticals
J. Le Roux
*Université de Poitiers, Laboratoire de Chimie et de Microbiologie de l'Eau (UMR CNRS 6008), École Supérieure d'Ingénieurs de Poitiers, 40 avenue du recteur Pineau, 86022 Poitiers cedex, France, (E-mail: julien.leroux@univpoitiers. fr, email@example.com)
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Water Practice and Technology (2010) 5 (4): wpt2010084.
J. Le Roux, H. Gallard, J.P. Croué; Formation of NDMA by Chloramination of Nitrogenous Pharmaceuticals. Water Practice and Technology 1 December 2010; 5 (4): wpt2010084. doi: https://doi.org/10.2166/wpt.2010.084
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