Abstract
After discussing the general aspects of photocatalytic oxidation of organic compounds in aqueous solutions and the application of the rotating disk theory to (photo)catalytic phenomena, we report the oxidation of p-nitrophenol (PNP) on illuminated phosphorus modified TiO2 (P-TiO2) and TiO2 photocatalysts under controlled hydrodynamic conditions. We found that the performance of the oxygen transfer reaction can be described considering mass transport in solution and surface reaction according to Langmuir–Hinshelwood kinetics. From analysis of the dependence of the reaction rate on the rotation rate, we obtained the apparent organic–photocatalyst adduct interaction constant K, the rate constant k of the surface reaction between adsorbed PNP and hydroxyl radicals, and the diffusion coefficient D of PNP in solution. The results showed that degradation of PNP using P-TiO2 and UV light was readily possible, with reaction half-lives significantly lower than those obtained using pristine TiO2 photocatalyst.
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