Abstract

Abstract Heterogeneous Fenton has become a promising economical and environmentally-friendly method for water treatment, however, the production of abundant radical resources (e.g., O2−, OH) are oftentimes limited by finite Fe2+ species to activate H2O2. Therefore, development of a new iron-bearing solid modified with diverse functional groups for generating a large of radicals in heterogeneous Fenton is significance. Here, we constructed a Fe3O4-modified schwertmannite (Fe3O4/Sch) catalyst to activate H2O2, SO42− and O2 to produce three kinds of radicals in heterogeneous Fenton reaction. Specifically, Fe3O4/Sch catalyst was synthesized to improve its surface properties such as the contents of surface Fe2+ species as H2O2 or O2 activators to produce OH or O2−, the SO42− of Sch surface as SO4 − precursor, and electron transfer between Fe3+ and Fe2+. Degradation rate of ciprofloxacin (CIP) for 6 min was up to 97% in Fe3O4/Sch-H2O2 system, which was higher than that in Sch-H2O2 or Fe3O4-H2O2. After four successive cyclic experiments, degradation rate of CIP was still achieved 97% within 10 min in Fe3O4/Sch-H2O2 system. The formation pathways of the relevant active radicals and the degradation pathways of CIP were also proposed by theoretically calculated and LC-MS data. This finding has not only developed an efficient heterogeneous Fenton catalyst, but also given a new idea of SO4 − generation by modified iron oxyhydroxysulfate mineral for application of heterogeneous Fenton technology.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.