| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 26114 | Journal of Photochemistry and Photobiology A: Chemistry | 2015 | 9 Pages |
•Oxacillin degradation by TiO2 photocatalysis was studied.•Effect of pH, TiO2 and pollutant concentration, and light intensity were evaluated.•Degradation in natural water and in a commercial product was tested.•The antimicrobial activity and the pollutant concentration were eliminated.•The main by-products were identified and degradation routes were elucidated.•The antibiotic was completely mineralized.
The TiO2 photocatalytic degradation of oxacillin (OXA) in synthetic and natural waters was studied. The matrix effects, in terms of antibiotic and antimicrobial activity removal, were evaluated in the presence of iron ions, natural mineral water and additives contained in commercial formulations of the antibiotic. A slight improvement in degradation was observed in the presence of iron ions. On the other hand, the presence of excipients in a commercial formulation or inorganic ions in natural mineral water slightly inhibited the efficiency of the system. An experimental design using pH, catalyst load and light intensity as variables was also evaluated. The best performances were achieved at natural pH (∼6.0) using 2.0 g L−1 of TiO2 with 150 W of applied power. The evaluation of OXA concentration indicated that the photodegradation process showed a Langmiur–Hinshewoold kinetic model. The extent of the process was evaluated following the evolution of chemical oxygen demand (COD) and dissolved organic carbon (DOC). Total removal of both, the antibiotic and its antimicrobial activity, was achieved after 120 min; while 100% of mineralization was observed within 480 min of treatment. Finally, five by-products were identified, the degradation routes were elucidated and a schema of the antibiotic degradation was proposed.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slide
