2004
DOI: 10.1021/es049580g
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Chlorination Byproduct Formation in the Presence of Humic Acid, Model Nitrogenous Organic Compounds, Ammonia, and Bromide

Abstract: The formation of trihalomethanes (THMs), haloacetic acids (HAAs), and cyanogen halides (CNXs) after chlorination of synthetic solutions containing humic acid, nitrogenous organic (N-organic) compounds, ammonia, and bromide ions was studied. Humic acid (from Aldrich) was used to provide the source of the precursors. Glycine was chosen as the primary model N-organic compound and other four model N-organic compounds (including glutamic acid, glycylglycine, diethylamine, and methylamine) were also evaluated for co… Show more

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Cited by 118 publications
(66 citation statements)
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“…Some of these techniques reduce the quality of water, and the side-products have an adverse effect on consumer health. Chlorine in water combines with natural organic compounds to yield substances such as trihalomethanes, haloacetic acids, and chlorophenols that exhibit potentially carcinogenic, teratogenic and mutagenic activities [6]. Ceramic water filtration is the process of passing water through a porous ceramic material.…”
Section: Introductionmentioning
confidence: 99%
“…Some of these techniques reduce the quality of water, and the side-products have an adverse effect on consumer health. Chlorine in water combines with natural organic compounds to yield substances such as trihalomethanes, haloacetic acids, and chlorophenols that exhibit potentially carcinogenic, teratogenic and mutagenic activities [6]. Ceramic water filtration is the process of passing water through a porous ceramic material.…”
Section: Introductionmentioning
confidence: 99%
“…A number of organics have been identified as THM precursors, such as HA [10], organic nitrogen compounds [11], citric acid [12], methyl ketones [13], algal cells [14], and hydroxybenzene [15]. HA is a main precursor with a complex macromolecule containing aromatic heterocyclic rings that are commonly substituted with methoxy (OMe), hydroxyl (OH), carboxylic (COOH), and other functional groups [16].…”
Section: Introductionmentioning
confidence: 99%
“…By contrast, cyanides could be directly converted into less harmful products by employing oxidation methods, such as ozonation [7], electrochemical oxidation [8,9], photocatalysis [10,11], ferrate oxidation [12,13] and wet oxidation [14]. The most practical method was thought to be alkaline chlorination, but it has many disadvantages such as formation of toxic cyanogens chloride [15] and chloride disinfection by-products [16].…”
Section: àmentioning
confidence: 99%