The effect of substituents on the oxidation of azo dyes in the Fe-III-EDTA-H2O2 system was examined at pH 7.4-(4'-sulfophenylazo)phenol and 2-(4'-sulfophenylazo)phenol, with methyl, methoxy, and halo substituents on the phenolic ring, were used as model systems. Oxidation of the naphthol dyes Orange I and Orange II were also examined. All of the dyes tested were decolorized in the Fe-III-EDTA-H2O2 system, but the degree of decolorization varied over a factor of 10. Dyes substituted with one or two halogens were oxidized to a greater extent than the corresponding methyl- or methoxy-substituted dyes. One explanation for the effect of halogen substituents is that they make the phenolic moieties more acidic, which favors the phenolate anion, which is more readily attacked by . OH. This explanation is supported by the observed correlation between charge density of the phenolate anion and the degree of decolorization. Based on an analysis of products formed from Orange II, a probable mechanism for decolorization of phenolic azo dyes by . OH is proposed. In addition, the optimal levels of H2O2 needed for the process have been examined. It appears that high levels of H2O2 could reduce decolorization by scavenging the . OH. (C) 2001 Elsevier Science Ltd. All rights reserved.