4.8 Article

Effect of FeCl3 on sulfonamide removal and reduction of antimicrobial activity of wastewater in a photocatalytic process with TiO2

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 126, Issue -, Pages 29-38

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2012.06.027

Keywords

Photocatalysis; Sulfonamides; Wastewater treatment; Antimicrobial activity; Photochemical treatment

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The aim of the study was to investigate the degradation of sulfonamides (SNs) in real wastewater samples using photocatalytic processes performed in the presence of a commercial TiO2 catalyst (Degussa Aeroxide P25), FeCl3 and a TiO2/FeCl3 mixture. The dynamics of the photodegradation of a mixture containing sulfadiazine, sulfamethoxazole and sulfathiazole in distilled water and in synthetic, municipal (raw and after treatment) wastewater, in wastewater from septic tank and in landfill leachate were compared during the study. The changes in the antimicrobial activity of the samples containing SNs and the photodegradation products were also assessed using the MARA (R) test. It was observed that the photocatalytic degradation rate of SNs was primarily dependent on the environmental pollution degree, the catalytic system composition and pH values. In a landfill leachate the SNs photodegradation practically did not proceed. The inhibitors of the process were primarily soluble wastewater components. The decomposition products of the SNs did not cause an increase in the antimicrobial activity of the reaction medium. The highest effectiveness for the photodegradation of SNs was obtained using the mixture containing TiO2 (similar to 0.5 g l(-1)) and FeCl3 (similar to 0.5 mmol l(-1)) at pH similar to 3.0. The activity of this catalyst system estimated based on the half-life values of the SNs in the investigated samples were approximately 4.5 times greater than that in the presence of TiO2 alone. Its high activity at pH similar to 3 primarily resulted from the decrease in the dissociation degree of other wastewater components in acidic medium, rather than the synergism of both photocatalyst components. (c) 2012 Elsevier B.V. All rights reserved.

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