Degradation of VOC gases in liquid phase by photocatalysis at the bubble interface

Photocatalytic reactions in the gas phase have a number of disadvantages including the adverse effects of relative humidity, the emission of decomposition intermediates at the reactor exit and the deactivation of the photocatalyst surface by decomposition intermediates. In this study, these disadvantages can be overcome using a novel photocatalytic reaction system. Volatile organic compound (VOC) gases were decomposed at the bubble interface in a TiO2 suspension by using TiO2 photocatalysis in the heterogeneous liquid-bubble (LB) phase since the intermediates dissolve into water and then are continuously decomposed regardless of humidity. Toluene, p-xylene, styrene and formaldehyde were chosen as model VOC gases to investigate photocatalytic reactivity in the LB phase. The removal ratio of VOC gases in the LB phase was equal to or greater than that in the gas phase, although the reactivity in the LB phase depended on the reaction rate of OH radicals and the hydrophobicity of the VOC gases. The reaction in the LB phase also depended on the wavelength and intensity of UV light. Specifically, the removal and mineralization ratios were improved by using shorter wavelengths of UV irradiation. Finally, as a trial experiment, we applied the microbubble technique to this system. When VOC gases were introduced into the system as microbubbles, VOC gas was effectively removed and high removal ratios were obtained regardless of the wavelength and intensity UV light.