Formation and reactivity of inorganic and organic chloramines and bromamines during oxidative water treatment
The formation and further reactions of halamines during oxidative water treatment can be relevant for water quality. In this study, we investigated the formation and reactivity of several inorganic and organic halamines (monochloramine, N-chloromethylamine, N-chlorodimethylamine, monobromamine, dibr...
| Main Authors: | , , , , |
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| Format: | Journal Article |
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IWA Publishing
2017
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| Online Access: | http://hdl.handle.net/20.500.11937/21223 |
| _version_ | 1848750529791918080 |
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| author | Heeb, M. Kristiana, Ina Trogolo, D. Arey, J. von Gunten, U. |
| author_facet | Heeb, M. Kristiana, Ina Trogolo, D. Arey, J. von Gunten, U. |
| author_sort | Heeb, M. |
| building | Curtin Institutional Repository |
| collection | Online Access |
| description | The formation and further reactions of halamines during oxidative water treatment can be relevant for water quality. In this study, we investigated the formation and reactivity of several inorganic and organic halamines (monochloramine, N-chloromethylamine, N-chlorodimethylamine, monobromamine, dibromamine, N-bromomethylamine, N,N-dibromomethylamine, and N-bromodimethylamine) by kinetic experiments, transformation product analysis, and quantum chemical computations. Kinetic model simulations were conducted to evaluate the relevance of halamines for various water treatment scenarios. Halamines were quickly formed from the reaction of chlorine and bromine with ammonia or organic amines. Species-specific second-order rate constants for the reaction of chlorine and bromine with ammonia, methyl- and dimethylamine were in the order of 106-108 M-1s-1. The formed halamines were found to be reactive towards phenolic compounds, forming halogenated phenols via electrophilic aromatic substitution (phenol and resorcinol) or quinones via electron transfer (catechol and hydroquinone). At near neutral pH, apparent second-order rate constants for these reactions were in the order of 10-4-10-1 M-1s-1 for chloramines and 101-102 M-1s-1 for bromamines. Quantum chemical computations were used to determine previously unknown aqueous pKa values, gas phase bond dissociation energies (BDE) and partial atomic charges of the halamines, allowing a better understanding of their reactivities. Kinetic model simulations, based on the results of this study, showed that during chlorination inorganic and organic chloramines are the main halamines formed. However, their further reactions with organic matter are outcompeted kinetically by chlorine. During ozonation, mainly inorganic bromamines are formed, since ozone quickly oxidizes organic amines. The further reactions of bromamine are typically outcompeted by ozone and thus generally of minor importance. The use of peracetic acid for saline ballast water treatment can result in the formation of substantial amounts of bromamines, which can react with dissolved organic matter and contribute to the formation of brominated products. |
| first_indexed | 2025-11-14T07:38:17Z |
| format | Journal Article |
| id | curtin-20.500.11937-21223 |
| institution | Curtin University Malaysia |
| institution_category | Local University |
| last_indexed | 2025-11-14T07:38:17Z |
| publishDate | 2017 |
| publisher | IWA Publishing |
| recordtype | eprints |
| repository_type | Digital Repository |
| spelling | curtin-20.500.11937-212232017-09-13T13:55:06Z Formation and reactivity of inorganic and organic chloramines and bromamines during oxidative water treatment Heeb, M. Kristiana, Ina Trogolo, D. Arey, J. von Gunten, U. The formation and further reactions of halamines during oxidative water treatment can be relevant for water quality. In this study, we investigated the formation and reactivity of several inorganic and organic halamines (monochloramine, N-chloromethylamine, N-chlorodimethylamine, monobromamine, dibromamine, N-bromomethylamine, N,N-dibromomethylamine, and N-bromodimethylamine) by kinetic experiments, transformation product analysis, and quantum chemical computations. Kinetic model simulations were conducted to evaluate the relevance of halamines for various water treatment scenarios. Halamines were quickly formed from the reaction of chlorine and bromine with ammonia or organic amines. Species-specific second-order rate constants for the reaction of chlorine and bromine with ammonia, methyl- and dimethylamine were in the order of 106-108 M-1s-1. The formed halamines were found to be reactive towards phenolic compounds, forming halogenated phenols via electrophilic aromatic substitution (phenol and resorcinol) or quinones via electron transfer (catechol and hydroquinone). At near neutral pH, apparent second-order rate constants for these reactions were in the order of 10-4-10-1 M-1s-1 for chloramines and 101-102 M-1s-1 for bromamines. Quantum chemical computations were used to determine previously unknown aqueous pKa values, gas phase bond dissociation energies (BDE) and partial atomic charges of the halamines, allowing a better understanding of their reactivities. Kinetic model simulations, based on the results of this study, showed that during chlorination inorganic and organic chloramines are the main halamines formed. However, their further reactions with organic matter are outcompeted kinetically by chlorine. During ozonation, mainly inorganic bromamines are formed, since ozone quickly oxidizes organic amines. The further reactions of bromamine are typically outcompeted by ozone and thus generally of minor importance. The use of peracetic acid for saline ballast water treatment can result in the formation of substantial amounts of bromamines, which can react with dissolved organic matter and contribute to the formation of brominated products. 2017 Journal Article http://hdl.handle.net/20.500.11937/21223 10.1016/j.watres.2016.11.065 IWA Publishing restricted |
| spellingShingle | Heeb, M. Kristiana, Ina Trogolo, D. Arey, J. von Gunten, U. Formation and reactivity of inorganic and organic chloramines and bromamines during oxidative water treatment |
| title | Formation and reactivity of inorganic and organic chloramines and bromamines during oxidative water treatment |
| title_full | Formation and reactivity of inorganic and organic chloramines and bromamines during oxidative water treatment |
| title_fullStr | Formation and reactivity of inorganic and organic chloramines and bromamines during oxidative water treatment |
| title_full_unstemmed | Formation and reactivity of inorganic and organic chloramines and bromamines during oxidative water treatment |
| title_short | Formation and reactivity of inorganic and organic chloramines and bromamines during oxidative water treatment |
| title_sort | formation and reactivity of inorganic and organic chloramines and bromamines during oxidative water treatment |
| url | http://hdl.handle.net/20.500.11937/21223 |