Ramírez-Sánchez, I.M.; Bandala, E.R. Photocatalytic Degradation of Estriol Using Iron-Doped TiO2 under High and Low UV Irradiation. Catalysts2018, 8, 625.
Ramírez-Sánchez, I.M.; Bandala, E.R. Photocatalytic Degradation of Estriol Using Iron-Doped TiO2 under High and Low UV Irradiation. Catalysts 2018, 8, 625.
Ramírez-Sánchez, I.M.; Bandala, E.R. Photocatalytic Degradation of Estriol Using Iron-Doped TiO2 under High and Low UV Irradiation. Catalysts2018, 8, 625.
Ramírez-Sánchez, I.M.; Bandala, E.R. Photocatalytic Degradation of Estriol Using Iron-Doped TiO2 under High and Low UV Irradiation. Catalysts 2018, 8, 625.
Abstract
Iron Doped TiO2 nanoparticles (Fe-TiO2) were synthesized and photocatalitically investigated under high and low fluence values of UV-radiation. The Fe-TiO2 physical characterization was performed using X-ray Powder Diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area analysis, Transmission Electron Microscope (TEM), Scanning Electron Microscope (SEM), Diffuse Reflectance Spectroscopy (DRS), and X-Ray Photoelectron Spectroscopy (XPS) technique. The XPS evidenced that ferric ion (Fe3+) was in the lattice of TiO2 and co-dopants no intentionally added were also present due to the precursors of the synthetic method. The Fe3+ concentration played a key role in the photocatalytic generation of hydroxyl radical (•OH) and estriol (E3) degradation. Fe-TiO2 materials accomplished E3 degradation, and it was found that the catalyst with 0.3 at. % content of Fe (0.3 Fe-TiO2) enhanced the photocatalytic activity under low UV-irradiation compared with no intentionally Fe-added TiO2 (zero-iron TiO2) and Aeroxide® TiO2 P25. Furthermore, the enhanced photocatalytic activity of 0.3 Fe-TiO2 under low UV-irradiation may have applications when radiation intensity must be controlled, as in medical applications, or when strong UV absorbing species are present in water.
Copyright:
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
