Photocatalytic degradation of chlorophenols on TiO2-325mesh and TiO2-P25. An extended kinetic study of photodegradation under competitive conditions

• Published in: Journal of photochemistry and photobiology. A, Chemistry. Chemistry., 2012-08, Vol.242, p.20-27
• Main Authors: Pino, Eduardo, Encinas, Maria Victoria
• Format: Article
• Language: English
• Subjects: Adsorption isotherm; Chlorophenols; Competitive degradation; Photocatalysis heterogeneous; Semiconductor size effect
• ISSN: 1010-6030; 1873-2666
• DOI: 10.1016/j.jphotochem.2012.05.019

A mixture of 2,6-DCP (constant at ∼10−4M) and different concentrations of [4-CP]: ((□) 1×10−5, and ((○) 5×10−5; show a competitive degradation on different TiO2-anatase. [Display omitted] ► The adsorption constant (K) for 2,6-DCP was higher than 4-CP. ► The degradation rate of chlorophenols mixture was slower using TiO2-P25 than TiO2-325mesh. ► During the degradation process the pH values decrease from 5.5 to 3.8. ► The mineralization was more efficient for commercial TiO2-P25 than TiO2-325mesh. The photodegradation kinetics UV/TiO2-mediated of 4-chlorophenol (4-CP) and 2,6-dichlorophenol (2,6-DCP) mixtures were analyzed and compared under the same experimental conditions with both individual chlorophenols. The aim of this study was to get a more realistic approach to the critical processes involved in the photoinduced heterogeneous catalysis of systems containing more than one contaminant in competitive conditions, and also evaluate the influence of the particle size using the commercial TiO2-325mesh and TiO2-P25 as catalysts. The determination of the equilibrium adsorption constants in dark showed that the adsorption of the 2,6-DCP is considerably higher with respect to the 4-CP in both TiO2 particles, but this relation decreases in the mixture of these pollutants. Several parameters influencing the reaction rate were studied including initial phenol concentration, catalyst loading, pH change, and particle size distribution. The degradation kinetics of individual phenols at low conversion showed a similar reactivity towards photogenerate hydroxyl radicals. In agreement with the reduced adsorption in the mixture, degradation rate of phenols was markedly lower in the mixture than that observed for the individual compounds. On the other hand, the photodegradation rate was higher on the TiO2-325mesh than on TiO2-P25, this is opposite to surface area of these particles indicating that other surface properties as pore size play an important role. The photoinduced degradation of these chlorophenols showed two main intermediate products that correspond to the degradation of each individual chlorophenols.