Chemosphere 2015-08-01

Transformation of triclosan to 2,8-dichlorodibenzo-p-dioxin by iron and manganese oxides under near dry conditions.

Jiafeng Ding, Mian Su, Cuiwei Wu, Kunde Lin

Index: Chemosphere 133 , 41-6, (2015)

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Abstract

Triclosan (TCS) is a broad-spectrum antibacterial agent widely used in household and personal care products and is frequently detected in the environment. Previous studies have shown that TCS could be converted to the more toxic compound 2,8-dichlorodibenzo-p-dioxins (2,8-DCDD) in photochemical reactions and incineration processes. In this study, we demonstrated the formation of 2,8-DCDD from the oxidation of TCS by α-FeOOH and a natural manganese oxides (MnOx) sand. Experiments at room temperature and under near dry conditions showed that Fe and Mn oxides readily catalyzed the conversion of TCS to 2,8-DCDD and other products. Approximately 5.5% of TCS was transformed to 2,8-DCDD by α-FeOOH in 45 d and a higher conversion percentage (6.7%) was observed for MnOx sand in 16d. However, the presence of water in the samples significantly inhibited the formation of 2,8-DCDD. Besides 2,8-DCDD, 2,4-dichlorphenol (2,4-DCP), 4-chlorobenzene-1,2-diol, 2-chloro-5-(2,4-dichlorophenoxy)benzene-1,4-diol, and 2-chloro-5-(2,4-dichlorophenoxy)-1,4-benzoquinone were identified in the reactions. The possible pathways for the formation of reaction products were proposed. This study suggests that Fe and Mn oxides-mediated transformation of TCS under near dry conditions might be another potential pathway for the formation of 2,8-DCDD in the natural environment.Copyright © 2015 Elsevier Ltd. All rights reserved.