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Degradation of Brilliant Green (BG) dye has been studied using Fenton reagent in the dark environment. The intensity of dye color was pH dependent with maximum absorbance at pH 6. N -de-alkylation caused dye decomposition which resulted in the reduction of absorbance. The rate of BG dye decolorization increased with an increase in the H 2 O 2 and Fe 2+ concentration. The presence of background ions commonly found in an industrial dyeing wastewater suppressed the efficiency of color, COD and TOC removal within 9 %. There was about 2.9-fold increase in biodegradability index after 30 min of reaction. The proposed mechanism showed the routes of dye degradation with low errors (−0.88 to 0.49 g mol −1 ) with respect to the exact mass. Dye degradation began with N -de-ethylation, and later was further cleaved to aromatic-amine, -acid, -alcohol and -additive products. Hydroquinone was originated by hydroxylation of N , N -diethyl aniline. An equilibrium cycle among quinone, hydroquinone and Fe(III)-hydroquinone was exhibited through the formation of charge transfer complex.
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Rao et al. (2015) studied this question.
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