Electrochemical degradation of a real textile wastewater using β-PbO2 and DSA® anodes

被引:192
作者
Aquino, Jose M. [1 ]
Rocha-Filho, Romeu C. [1 ]
Ruotolo, Luis A. M. [2 ]
Bocchi, Nerilso [1 ]
Biaggio, Sonia R. [1 ]
机构
[1] Univ Fed Sao Carlos, Dept Quim, BR-13560970 Sao Carlos, SP, Brazil
[2] Univ Fed Sao Carlos, Dept Engn Quim, BR-13560970 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Real textile effluent; Wastewater electrochemical treatment; Textile wastewater remediation; Dye electrooxidation; Chloride-mediated oxidation; BORON-DOPED DIAMOND; RED; 141; DYE; LEAD DIOXIDE; ACTIVE CHLORINE; OXIDATION; REMOVAL; FENTON; DECOLORIZATION; WASTEWATERS; ELECTRODE;
D O I
10.1016/j.cej.2014.04.032
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The electrochemical degradation of a real textile effluent was carried out using Ti-Pt/beta-PbO2 and Ti/Ti(0.7-)wRu(0.3)O(2) (DSA (R)) anodes in a filter-press flow cell, in the presence and absence of chloride ions, varying, the pH (3, 7, 11) and temperature (25 degrees C and 45 degrees C) of the effluent, and monitoring the removal of its turbidity and chemical oxygen demand (COD). The best experimental conditions for turbidity and COD removal were attained in neutral and basic conditions, independently of temperature. Higher COD removal values were attained with the Ti-Pt/beta-PbO2 anode, as a consequence of its higher oxidation power; the electric charge applied per unit volume of effluent significantly decreased in the presence of chloride ions, when instantaneous current efficiencies as high as 0.5 were attained in the initial electrooxidation stages. Under these conditions, the electric energy consumption necessary to oxidize the real textile effluent was as low as 50 kW h m(-3). The use of chloride ions enabled higher COD removal efficiencies using the Ti-Pt/beta-PbO2 and DSA (R) anodes than a purely mass-transport controlled process due to indirect oxidation processes mediated by the active chloro species. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:138 / 145
页数:8
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