Assessing the electrochemical degradation of reactive orange 84 with Ti/IrO 2 -SnO 2 -Sb 2 O 5 anode using electrochemical oxidation, electro-Fenton, and photoelectro-Fenton under UVA irradiation.

Today, water shortage problems around the world have forced the search for new treatment alternatives, in this context, electrochemical oxidation technology is a hopeful process for wastewater treatment, although it is still needed exploration of new efficient and economically viable electrode materials. In this way, mixed metal oxide anodes look like promising alternatives but their preparation is still a significant point to study, searching for finding low-cost materials to improve electrocatalytic efficiencies. In an exploration of this kind of highly efficient materials, this work presents the results obtained using an MMO Ti/IrO ₂ -SnO ₂ -Sb ₂ O ₅ anode. All the prepared anodes exhibited excellent physical and electrochemical properties. The electrochemical oxidation of 100 mL and 200 mg L ^-1 Reactive Orange 84 (RO 84) diazo dye was studied using 3 cm ² of such synthesized anodes by applying current densities of 25, 50, and 100 mA cm ^-2 . Faster and more efficient electrochemical oxidation occurred at 100 mA cm ^-2 with 50 mM of Na ₂ SO ₄ + 10 mM NaCl as supporting electrolyte at pH 3.0. The degradation and mineralization processes of the above solution were enhanced with the electro-Fenton process with 0.05 mM Fe ²⁺ and upgraded using photoelectron-Fenton with UVA light. This process yielded 91% COD decay with a low energy consumption of 0.1137 kWh (g COD) ^-1 at 60 min. The evolution of a final carboxylic acid like oxalic was followed by HPLC analysis. The Ti/IrO ₂ -SnO ₂ -Sb ₂ O ₅ is then an efficient and low-cost anode for the photoelectro-Fenton treatment of RO 84 in a chloride and sulfate media.
Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
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