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contributor authorDing Wang
contributor authorJames R. Bolton
contributor authorSusan A. Andrews
contributor authorRon Hofmann
date accessioned2017-12-30T12:54:28Z
date available2017-12-30T12:54:28Z
date issued2016
identifier other%28ASCE%29EE.1943-7870.0001045.pdf
identifier urihttp://138.201.223.254:8080/yetl1/handle/yetl/4243235
description abstractHydrogen peroxide is a potential dechlorinating agent that can preserve chlorinated drinking water samples for the determination of disinfection by-products (DBPs). The impact of hydrogen peroxide on the storage of trihalomethanes (THMs), haloacetic acids (HAAs), haloacetonitriles (HANs), and adsorbable organic halides (AOX) generated by chlorination in a model of natural water was investigated and compared with parallel samples quenched by sodium sulfite and ammonium sulfate. Positive errors of up to 9  μg/L for THMs, 19  μg/L for HAAs, 1  μg/L for HANs, and 22  μg Cl/L for AOX were found after adding ammonium and storing for 9 days at 4°C, primarily due to the continued formation of chloroform, bromodichloromethane, dichloro- and trichloro-acetic acids, and dichloroacetonitrile. Hydrogen peroxide and sulfite led to smaller errors in the determination of THMs, HAAs, and AOX, while HANs degraded in the presence of sulfite. Hydrogen peroxide was the most suitable dechlorinating agent of these three for preserving THM, HAA, HAN, and AOX samples, provided that the relatively slow chlorine quenching reaction time (e.g., 3–4 min) is acceptable.
publisherAmerican Society of Civil Engineers
titleComparison of Hydrogen Peroxide to Ammonium Ions and Sulfite as a Free Chlorine Quenching Agent for Disinfection By-Product Measurement
typeJournal Paper
journal volume142
journal issue7
journal titleJournal of Environmental Engineering
identifier doi10.1061/(ASCE)EE.1943-7870.0001045
page06016002
treeJournal of Environmental Engineering:;2016:;Volume ( 142 ):;issue: 007
contenttypeFulltext


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