Søgaard, Erik Gydesen1; Simonsen, Morten Enggrob4; Jensen, Henrik5; Li, Zheshen7
1 Section of Chemical Engineering, The Faculty of Engineering and Science, Aalborg University, VBN2 CIChem Research Group (Colloid and Interface Chemistry), The Faculty of Engineering and Science, Aalborg University, VBN3 Esbjerg Institute of Technology, Aalborg University, The Faculty of Engineering and Science (ENG), Aalborg University, VBN4 Department of Chemistry and Bioscience, The Faculty of Engineering and Science, Aalborg University, VBN5 SCF-Technologies A/S, Valby6 Aarhus University7 Aarhus University
In this work two immobilizations techniques of TiO2 onto glass were investigated; deposition of previously made titania powder (PMTP) and a sol-gel method. The titania powder used in this work was Degussa P25, Hombikat UV100 and a powder prepared in our laboratory SC134. The prepared TiO2 films were characterized using XRD, XPS, AFM, UV-Vis spectroscopy and the photocatalytic activity was assessed using stearic acid as a model compound. Investigation of the prepared films showed that the films prepared from Degussa P25 was the most active, followed by the Hombikat UV100 film, Sol-gel film, and SC134 film. The activity of the films is assumed to be related to the crystallinity of the TiO2 as no major differences were found between the films using XPS analysis. Based on XPS investigation of the films before and after UV irradiation it was suggested that the photocatalytic destruction of stearic acid proceeds partly through formation of hydroxyl radicals which are formed from adsorbed hydroxyl groups. The investigation also showed that the rate of degradation increases linearly with the concentration of TiO2 in the films, these findings suggests that the amount of TiO2 in the film is the limiting condition for the rate of reaction. Also a new type of continuous photoreactor was developed in which the TiO2 catalyst made from Sol-gel film was immobilized on the surface of quartz tubes surrounding the UV lamps and on the internal surface of the reactor walls. The study showed that an initial concentration chloroform of 7 mg/l was degraded in a period of 500 hour. The kinetics of the degradation of chloroform in the flow reactor was found to obey Langmuir-Hinshelwood kinetics. The investigation also showed that the reactor design has a significant influence on the rate of degradation, as it was observed that the position of the coated lamp in the reactor yield different degradation rates.
Abstracts: 11th International Conference on Tio2 Photocatalysis: Fundamentals & Applications. - the 12th International Conference on Advanced Oxidation Technologies for Treatment of Water, Air and Soil, 2006
TiO2; photocatalysis; reactor; thin films
Main Research Area:
The 11th International Conference on TiO2 Photocatalysis: Fundamentals & Applications, 2006