Poor indoor air quality is a source of adverse health effects. TiO2 coatings deposited on well-illuminated surfaces, such as window panes, can be used to fully mineralize indoor air pollutants by photocatalysis. In such applications it is important to ensure stable photocatalytic activity for a wide range of operating conditions, such as relative humidity and temperature, and to avoid deactivation of the catalyst. In this thesis photocatalytic removal of the indoor-pollutant acetaldehyde (CH3CHO) on nanostructured TiO2 films is investigated, and in particular it is proposed how such films can be modified and operated for maximum performance. Catalyst deactivation can be reduced by purposefully changing the surface acidity of TiO2 by covalently attaching SO4 to the surface. Moreover, the overall photocatalytic activity on anatase TiO2 films can be improved by increasing the fraction of exposed reactive {001} surfaces, which otherwise are dominated by {101} surfaces. In the first part of the thesis mode-resolved in-situ FTIR is used to elucidate the reaction kinetics of CH3CHO adsorption and photo-oxidation on the TiO2 and SO4 – modified TiO2 surfaces. Surface concentrations of main products and corresponding reaction rates were determined. Formate is the major reaction product, whose further oxidation limits the complete oxidation to gaseous species, and is responsible for photocatalyst deactivation by site inhibition. The oxidation reaction is characterized by two reaction pathways, which are associated with two types of surface reaction sites. On the sulfate modified TiO2 catalyst fewer intermediates are accumulated, and this catalyst resists deactivation much better than pure TiO2. A hitherto unknown intermediate – surface-bound acetaldehyde dimer with an adsorption band at 1643 cm−1 was discovered, using interplay between FTIR spectroscopy and DFT calculations. The second part of the thesis treats the effect of increasing the relative abundance of exposed {001} facets on the photocatalytic activity of anatase TiO2 films prepared by DC magnetron sputtering. A positive effect was observed both for liquid-phase photo-oxidation of methylene blue, and for gas-phase photocatalytic removal of CH3CHO. In both cases it was found that the exposed {001} surfaces were an order of magnitude more reactive, compared to the {101} ones. Furthermore, it was found that the reactive films were more resilient towards deactivation, and exhibited almost unchanged activity under varying reaction conditions. Finally, a synergetic effect of SO4 – modification and high fraction of exposed {001} surfaces was found, yielding photocatalysts with sustained high activity. The results presented here for facet controlled and chemically modified TiO2 films are of interest for applications in the built environment for indoor air purification and as self-cleaning surfaces. / GRINDOOR

Master of Science / Department of Chemical Engineering / Larry E. Erickson / Photocatalytic oxidation (PCO) is a promising and emerging technique in controlling indoor air contaminants, including volatile organic compounds (VOCs). It has broad air cleaning and deodorization applications in indoor environments ranging from residential and office buildings to healthcare and nursing facilities as well as spacecrafts, aircraft cabins and clean rooms in the agricultural and food industry. Numerous studies have been conducted to improve the effectiveness and performance of this technology. These include development of new configurations, energy-efficient catalysts and other parameters to control the process. However, only limited research has been conducted under realistic indoor environmental conditions. One of the most recent developments in photocatalysis is the synthesis of 2% C- and V-doped TiO[subscript]2, which is active under both dark and visible light conditions. However, like most research conducted in photocatalysis, the study on the reactivity of this catalyst has been performed only under laboratory conditions. This study investigated the possible application of the novel C and V co-doped TiO[subscript]2 in cleaning indoor air. Mathematical modeling and simulation techniques were employed to assess the potential use of some of the promising systems that utilize the catalyst (i.e., packed bed and thin films) as well as the effect of mass transfer limitations in the degradation of acetaldehyde, one of the VOCs that can be found in offices, residential buildings and other facilities.