Photodegradation and Mineralization of Phenol Using TiO2Coated γ-Al2O3: Effect of Thermic Treatment
C. Martínez-Gómez, I. Rangel-Vázquez, Ramón Zárraga, Gloria Del Ángel, B. Ruiz-Camacho, Francisco Tzompantzi, Esmeralda Vidal-Robles, Alejandro Pérez‐Larios
Abstract
It is well-known that γ-Al2O3 possesses large, specific areas and high thermal, chemical, and mechanical resistance. Due to this, it is the most-used support for catalysts, in this case TiO2, as it enables it to achieve better dispersion and improves the activity in catalytic photodegradation reactions. In a previous work, it was observed that the optimal content of TiO2 in γ-Al2O3 was around 15% since the degradation of phenol results were maximized and a synergistic effect was generated by the interaction of both oxides. In addition, an increase in acidity crystal size and the generation of localized, oxygen-vacant, electronic states in the forbidden band of γ-Al2O3, were observed. This study focuses on the effect of the calcination temperature on a γ-Al2O3-TiO2 catalyst (15% w/w of TiO2) and its impact on photocatalytic activity. The catalysts prepared here were characterized by X-ray diffraction, N2 adsorption–desorption, FTIR-pyridine adsorption, MAS-NMR, HRTEM-FFT, UV-vis, and fluorescence spectroscopy.