Electrogeneration of Active Chlorine in a Filter-Press-Type Reactor Using a New Sb2O5 Doped Ti/RuO2-ZrO2 Electrode: Indirect Indigoid Dye Oxidation
Abstract This paper presents the study on active chlorine mediated electrochemical oxidation of model solutions that simulate textile effluents containing an indigoid dye (indigo carmine) and sodium chloride (0.05 M) using a new Sb2O5-doped Ti/RuO2-ZrO2 electrode. The study was carried out in a filter-press electrochemical reactor specially designed to minimize flow deviations and provide homogeneous mass transfer flux over the electrode surface. Firstly, the mass-transfer-limited chloride oxidation reaction was studied in the absence of dye in order to understand the active chlorine formation process. Changes in pH, chloride concentration and UV-visible absorption spectra during electrolysis reveal the formation of active chlorine (mainly hypochlorite) with current efficiencies for chloride oxidation of 0.558 and 0.503 at 10 and 20 mA cm−2, respectively. Secondly, chloride oxidation was investigated in the presence of indigo carmine dye (0.5 mM) where in-situ generated active chlorine was responsible for -C=C- bond breaking and dye degradation. The solution discoloration followed a pseudo-first order kinetics where kinetic coefficient was inversely proportional to dye concentration. The oxidation with active chlorine had an average efficiency of 0.7 and a very competitive energy consumption between 49.2 and 128.5 kW h (kg COD removed)−1 depending on current density and flow rate.