| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6307144 | Chemosphere | 2016 | 6 Pages |
Abstract
Reaction of 2-aminophenol (2AP) with monochloramine in aqueous solution was investigated at pH 8.5 and 25 °C, with an excess of monochloramine. 2-Amino-3H-phenoxazin-3-one (APO) was the major product formed in about 70% yield. Despite low formation yields, adsorbable organic halides (AOX) were also formed over reaction time.
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Authors
Odissa Abou Mehrez, Florence Dossier-Berne, Bernard Legube,