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Process optimization and mechanism study of acid red G degradation by electro-Fenton­Feox process as an in situ generation of H(2)O(2)

Dye-contaminated wastewaters are industrial wastewaters that are difficult to treat using traditional biochemical and physicochemical methods. In the present work, the acid red G was removed as a model pollutant by the electro-Fenton process for the first time. The anode and cathode used by the elec...

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Detalles Bibliográficos
Autores principales: SUN, Hailong, YAO*, Yingwu, WEI, Feng, ZHAO, Qiang, LIU, Baichen, ZHANG, Liman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7925314/
https://www.ncbi.nlm.nih.gov/pubmed/33679147
http://dx.doi.org/10.3906/kim-2002-10
Descripción
Sumario:Dye-contaminated wastewaters are industrial wastewaters that are difficult to treat using traditional biochemical and physicochemical methods. In the present work, the acid red G was removed as a model pollutant by the electro-Fenton process for the first time. The anode and cathode used by the electro-Fenton process were iron plate and graphite felt, respectively. It was concluded that under the optimal conditions of current density = 20 mA cm(-2), pH = 3 and initial Na(2)SO(4) concentration = 0.2 M, the removal rate of acid red G (ARG) with an initial concentration of 300 mg L(-1) could reach 94.05% after 80 min of electrolysis. This reveals that the electro-Fenton-Feox process used in this work has an excellent removal efficiency on acid red G. The required reagents (Fe(2+) and H(2)O(2)) were generated by the electrode reaction, while the optimal generation conditions and mechanism of •OH, H(2)O(2), and Fe(2+) were investigated. By testing •OH, H(2)O(2), and Fe(2+) agents at different pH and current densities, it was revealed that the electro-Fenton reaction was most efficient when the current density was 20 mA cm(-2), and the pH was 3. Moreover, the removal rate of ARG is consistent with first-order reaction kinetics.