Abstract

In this study visible light active iodine doped titanium dioxide samples prepared by sol–gel method were investigated. Photocatalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray fluorescence spectroscopy (XFS), diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS) and by Brunauer–Emmett–Teller (BET) surface area technique.Different iodine/titanium ratios (nI/nTi=0.0–2.6) were applied during the synthesis and the optimum value was determined by phenol degradation under UV and VIS irradiations. The photocatalytic efficiency towards phenol degradation and the inactivation of Escherichia coli (E. coli) contaminated water under visible light illumination (conventional 24W energy-saving compact fluorescence lamps) of the most active iodine-doped TiO2 (nI/nTi=0.5; 79.5m2/g; 98wt% anatase) was compared with well known reference photocatalysts, that are Aeroxide P25 and Aldrich anatase (>85nm primary crystallite size). Results showed that our iodine doped TiO2 was far more efficient at inactivating the E. coli and decomposing the phenol than Aeroxide P25. Electron spin resonance (ESR) measurements confirmed the formation of highly reactive OH radicals by the iodine doped titania under VIS irradiation. In contrast, singlet oxygen and superoxide radical ions were not detected. The performed experiments also proved that dissolved iodine was produced in very low concentrations (about 0.01–0.025mg/L) from the irradiated titanium dioxide. The dissolved iodine could have some contribution to the phenol oxidation and the disinfection effects. This study demonstrated this property of iodine-doped titanias for the first time.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.