Examination of Photocatalyzed Chlorophenols for Sequential Photocatalytic-Biological Treatment Optimization

Abstract

Given the known adverse effect of chlorophenols for the aquatic environments which they can reach, the development of efficient methods both technically and economically to remove them has gained increasing attention over time. The combination of photocatalytic oxidation with biological treatment can lead to high removal efficiencies of chlorophenols, while reducing the costs associated with the need to treat large volumes of aqueous solutions. Therefore, the present paper had as its main objective the identification of the minimum photocatalytic oxidation period during which the aqueous solutions of 4-chlorophenol and 2,4-dichlorophenol can be considered as readily biodegradable. Thus, the results of photocatalytic oxidation and biodegradability tests showed that, regardless of the concentration of chlorophenol and its type, the working solutions become readily biodegradable after up to 120 min of irradiation in ultraviolet light. At this irradiation time, the maximum organic content of the aqueous solution is less than 40%, and the biochemical oxygen demand and chemical oxygen demand (BOD/COD) ratio is much higher than 0.4. The maximum specific heterotrophic growth rate of activated sludge has an average value of 4.221 d−1 for 4-chlorophenol, and 3.126 d−1 for 2,4-dichlorophenol. This irradiation period represents at most half of the total irradiation period necessary for the complete mineralization of the working solutions. The results obtained were correlated with the intermediates identified during the photocatalytic oxidation. It seems that, working solutions initially containing 4-chlorophenol can more easily form readily biodegradable intermediates.