Abstract This work assesses the role of the operational conditions upon the electro-activation of persulfate (electro-PS) using Ti/IrO2 Ta2O5 electrode for the decolorization of anthraquinone azo dye Disperse Blue 3… Click to show full abstract
Abstract This work assesses the role of the operational conditions upon the electro-activation of persulfate (electro-PS) using Ti/IrO2 Ta2O5 electrode for the decolorization of anthraquinone azo dye Disperse Blue 3 (DB3). The studied variables include current density (j) (5–80 mA cm−2), persulfate concentration based on the stoichiometric dose for complete DB3 mineralization (20–100%), temperature (30–90 °C) and pH (3–12) as well as the influence of dissolved oxygen. The persulfate activation from cathodic reduction was confirmed by linear sweep voltammetry (LSV). The increase in j enhanced the PS decomposition and, consequently, decolorization efficiency, because of the greater production of sulfate radicals (SO4•−). Besides, the combination of electro-PS with thermal activation resulted in a synergistic effect upon the DB3 mineralization. In the range 30–70 °C, electro-PS led to a significantly higher TOC conversion (above 60% at 40 mA cm−2) than sole heat-activated PS. This difference steeply decreased as temperature increases, achieving similar TOC conversion at 90 °C after 60 min.
               
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