ndeprtarea compuilor organici refractari din ape uzate nc reprezint un
subiect de interes, cercetrile fiind concentrate pe identificarea unor procedee care s fie eficiente att din punct de vedere tehnic ct i din punct de vedere economic. Astfel, combinarea unei prime etape de oxidare avansat, n care compuii iniali sunt transformai n compui cu biodegradabilitate mare, cu o a doua etap de epurare biologic pare a fi o soluie eficient pentru rezolvarea acestei probleme. Optimizarea acestui procedeu de epurare impune un studiu amnunit al intermediarilor formai n etapa de oxidare avansat n scopul identificrii mecanismelor de degradare a compuilor iniiali i a timpilor optimi de iradiere. n acest sens, n lucrarea de fa sunt prezentate rezultatele experimentale obinute cu privire la identificarea intermediarilor i a mecanismelor de degradare a 2,4- diclorfenolului din soluii apoase n procese de oxidare fotocatalitic utiliznd drept catalizator TiO 2 depus pe suport de titan. Rezultatele obinute indic trei posibile mecanisme de degradare i anume mecanismul 2-clorhidrochinonei, mecanismul 3,5-diclorcatecholului i mecanismul 4-clorfenolului. Aceste rezultate sunt n concordan cu rezultatele experimentale obinute n cadrul unor studii anterioare de epurare biologic efectuate pe soluii apoase de 2,4-diclorfenol rezultate la diferii timpi de iradiere n procesul fotocatalitic indicnd faptul c intermediarii formai sun uor biodegradabili i astfel uor de ndeprtat n etapa de epurare biologic.
Abstract Removal of refractory organic compounds from wastewater still represents an interesting topic, the research being focused on identifying some techniques that to be efficient from both technical and economic standpoint. Thus, combining of a first-stage of advanced oxidation, in which the initial compounds are converted into compounds of higher biodegradability, with a second-stage of biological treatment, appears to be an effective solution to this problem. Optimizing of this treatment technique requires a detailed study of the intermediates formed in the first-stage of advanced oxidation in order to identify the degradation mechanisms of initial compounds and the optimal times of irradiation. In this respect, the paper presents the experimental results regarding the identification of intermediates and mechanisms of degradation of 2,4-dichlorophenol in aqueous solutions during the process of photocatalytic oxidation using TiO 2 as catalyst supported on titanium. The results indicate three possible mechanisms of degradation, namely the mechanism of 2-chlorohydroquinone, the mechanism of 3,5-dichlorocatechol, and the mechanism of 4-chlorophenol. These results are in good agreement with the experimental results obtained in earlier studies regarding the biological treatment of 2,4-dichlorophenol at different times of irradiation, indicating that the resulted intermediates are readily biodegradable and therefore easily removed in the second-stage of biological treatment.