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Enhanced catalytic degradation of ciprofloxacin with FeS2/SiO2 microspheres as heterogeneous Fenton catalyst: Kinetics, reaction pathways and mechanism.
- Source :
-
Journal of Hazardous Materials . Apr2017, Vol. 327, p108-115. 8p. - Publication Year :
- 2017
-
Abstract
- In this study, the application of FeS 2 /SiO 2 microspheres as a catalyst to activate H 2 O 2 for the degradation of ciprofloxacin (CIP) was systematically investigated. Results demonstrated that the presence of SiO 2 microspheres on the surface of FeS 2 could effectively make the reaction of aqueous Fe 2+ and H 2 O 2 smoothly continuous by controlling the release of aqueous Fe 2+ from FeS 2 . Nearly 100% of CIP was degraded after 60 min under the optimum conditions. A superior performance on the CIP degradation and high reusability of the catalyst was obtained in FeS 2 /SiO 2 microspheres activated H 2 O 2 system. A low concentration of ethylene diamine tetraacetie acid (EDTA) did positively affect the degradation rate of CIP. A synergetic effect between adsorption and oxidation processes contributed to the significant enhancement of CIP degradation. Seven oxidation intermediates were identified during the CIP degradation process, and the direct HO oxidation proved to be a main CIP degradation pathway. For degradation pathway of CIP, oxidation of piperazine ring would be its first step, followed by cleavage of the heterocyclic ring. Subsequently, the substitution, hydroxylation and decarboxylation processes occurred. This is the first report on the feasibility of FeS 2 /SiO 2 microspheres activated H 2 O 2 system for the enhanced degradation of CIP. [ABSTRACT FROM AUTHOR]
- Subjects :
- *MICROSPHERES
*CHEMICAL kinetics
*CIPROFLOXACIN
*AQUEOUS solutions
*DECARBOXYLATION
Subjects
Details
- Language :
- English
- ISSN :
- 03043894
- Volume :
- 327
- Database :
- Academic Search Index
- Journal :
- Journal of Hazardous Materials
- Publication Type :
- Academic Journal
- Accession number :
- 120888236
- Full Text :
- https://doi.org/10.1016/j.jhazmat.2016.12.045