Electrochemical oxidation of acid black 210 dye on the boron-doped diamond electrode in the presence of phosphate ions: Effect of current density, pH, and chloride ions

被引:128
作者
Costa, Carla Regina [1 ]
Montilla, Francisco [2 ]
Morallon, Emilia [2 ]
Olivi, Paulo [1 ]
机构
[1] Univ Sao Paulo, Fac Filosofia Ciencias & Letras Ribeirao Preto, Dept Quim, BR-14040901 Ribeirao Preto, SP, Brazil
[2] Univ Alicante, Dept Quim Fis, E-03080 Alicante, Spain
基金
巴西圣保罗研究基金会;
关键词
Boron-doped diamond; Acid black 210 dye; Hydroxyl radical; Peroxodiphosphate; Active chlorine; WASTE-WATER TREATMENT; THIN-FILM ELECTRODES; ORGANIC POLLUTANTS; ANODIC-OXIDATION; AQUEOUS-SOLUTION; ACTIVE CHLORINE; REACTIVE DYES; DEGRADATION; RADICALS; MINERALIZATION;
D O I
10.1016/j.electacta.2009.07.027
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
070208 [无线电物理];
摘要
The electrochemical oxidation of acid black 210 dye (AB-210) on the boron-doped diamond (BDD) was investigated under different pH conditions. The best performance for the AB-210 oxidation occurred in alkaline phosphate solution. This is probably due to oxidizing agents such as phosphate radicals and peroxodiphosphate ions, which can be electrochemically produced with good yields on the BDD anode, mainly in alkaline solution. Under this condition, the COD (chemical oxygen demand) removal was higher than that obtained from the model proposed by Comninellis. Electrolyses performed in phosphate buffer and in the presence of chloride ions resulted in faster COD and color removals in acid and neutral solutions, but in alkaline phosphate solution, a better performance in terms of TOC removal was obtained in the absence of chloride. Moreover, organochloride compounds were detected in all electrolyses performed in the presence of chloride. The AB-210 electrooxidation on BDD using phosphate as supporting electrolyte proved to be interesting since oxidizing species generated from phosphate ions were able to completely degrade the dye without producing organochloride compounds. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:7048 / 7055
页数:8
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