Literature DB >> 27998787

Formation and reactivity of inorganic and organic chloramines and bromamines during oxidative water treatment.

Michèle B Heeb1, Ina Kristiana2, Daniela Trogolo1, J Samuel Arey3, Urs von Gunten4.   

Abstract

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.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Bromamines; Chloramines; Kinetic modeling; Oxidative water treatment; Partial charge; pK(a)

Mesh:

Substances:

Year:  2016        PMID: 27998787     DOI: 10.1016/j.watres.2016.11.065

Source DB:  PubMed          Journal:  Water Res        ISSN: 0043-1354            Impact factor:   11.236


  4 in total

1.  An increase in surface hydrophobicity mediates chaperone activity in N-chlorinated RidA.

Authors:  Marharyta Varatnitskaya; Julia Fasel; Alexandra Müller; Natalie Lupilov; Yunlong Shi; Kristin Fuchs; Marco Krewing; Christoph Jung; Timo Jacob; Barbara Sitek; Julia E Bandow; Kate S Carroll; Eckhard Hofmann; Lars I Leichert
Journal:  Redox Biol       Date:  2022-05-07       Impact factor: 10.787

2.  Challenges and opportunities for on-line monitoring of chlorine-produced oxidants in seawater using portable membrane-introduction Fourier transform-ion cyclotron resonance mass spectrometry.

Authors:  Adrien Roumiguières; Stéphane Bouchonnet; Said Kinani
Journal:  Anal Bioanal Chem       Date:  2020-11-19       Impact factor: 4.142

3.  Site-Selective C-H Halogenation Using Flavin-Dependent Halogenases Identified via Family-Wide Activity Profiling.

Authors:  Brian F Fisher; Harrison M Snodgrass; Krysten A Jones; Mary C Andorfer; Jared C Lewis
Journal:  ACS Cent Sci       Date:  2019-10-24       Impact factor: 14.553

4.  Synthesis and characterization of an α-Fe2O3/ZnTe heterostructure for photocatalytic degradation of Congo red, methyl orange and methylene blue.

Authors:  Rooha Khurram; Zhan Wang; Muhammad Fahad Ehsan; Song Peng; Maryam Shafiq; Bushra Khan
Journal:  RSC Adv       Date:  2020-12-21       Impact factor: 4.036

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.