US EPA

864614 

Journal Article 

Free-radical chemistry of disinfection byproducts. 3. Degradation mechanisms of chloronitromethane, bromonitromethane, and dichloronitromethane 

Mincher, BJ; Mezyk, SP; Cooper, WJ; Cole, SK; Fox, RV; Gardinali, PR 

2010 

1 

Journal of Physical Chemistry A
ISSN: 1089-5639
EISSN: 1520-5215 

AMER CHEMICAL SOC 

WASHINGTON 

114 

1 

117-125 

English 

20055512 

10.1021/jp907305g 

WOS:000273268900016 

Halonitromethanes (HNMs) are byproducts formed through ozonation and chlorine/ chloramine disinfection processes in drinking waters that contain dissolved organic matter and bromide ions. These species occur at low concentration but have been determined to have high cytotoxicity and mutagenicity and therefore may represent a human health hazard. In this study, we have investigated the chemistry involved in the mineralization of HNMs to nonhazardous inorganic products through the application of advanced oxidation and reduction processes. We have combined measured absolute reaction rate constants for the reactions of chloronitromethane, bromonitromethane, and dichloronitromethane with the hydroxyl radical and the hydrated electron with a kinetic computer model in an attempt to elucidate the reaction pathways of these HNMs. The results are compared to measurements of stable products resulting from steady-state (60)Co gamma-irradiations of the same compounds. The model predicted the decomposition of the parent compounds and ingrowth of chloride and bromide ions with excellent accuracy, but the prediction of the total nitrate ion concentration was slightly in error, reflecting the complexity of nitrogen oxide species reactions in irradiated solution.