Coupling of the electrochemical oxidation (EO-BDD)/photocatalysis (TiO2-Fe-N) processes for degradation of acid blue BR dye
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Morales Muñoz, Ulises; Escudero Santiago, Carlos Javier; Rivero Martínez, María José

Fecha
2018-01-01Derechos
© 2018, Elsevier. Licensed under the Creative Commons Reconocimiento-NoComercial-SinObraDerivada
Publicado en
Journal of Electroanalytical Chemistry, 2018, 808, 180-188
Editorial
Elsevier
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Palabras clave
Wastewater treatment
Fe-N codoped TiO2
Photoelectrocatalysis
Synergistic effect
Resumen/Abstract
We report on the successful preparation of Fe-N codoped Titania powders, using TiO2Degussa P25, salt of Fe (II), and Urea. Modified Titania-based materials were characterized by SEM, EDS, BET, Raman, XRD diffraction and diffuse reflectance UV–vis spectroscopy measurements. The doping of TiO2 induced a shift in the absorption threshold toward the spectral range, obtaining catalysts with a greater photoactivity than the one of pure Degussa P25. The degradation of 200 mL of a solution with 50 mg L− 1acid blue BR dye in sulfate medium at pH 3.0 has been comparatively studied by electrochemical oxidation using a boron doped diamond anode (EO-BDD), Photocatalysis TiO2-Fe-N, and coupled material of EO-BDD/Photocatalysis TiO2-Fe-N. The solution was slowly degraded by EO-BDD (25%) and single Photocatalysis TiO2-Fe-N because of the low rate of dye degradation and its colored by-products with hydroxyl radicals generated at the BDD anode and catalyst surface from water oxidation (29%), whereas the solution was more rapidly degraded using coupled material of EO-BDD/Photocatalysis TiO2-Fe-N (82%), owing to the additional generation of hydroxyl radicals from the photocatalysis of TiO2-Fe-N and BDD anode.
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