Abstract

In this work, composition-adjusted manganese ferrites (MnxFe3−xO4) were synthesized by a simple one-step solvothermal route and characterized by ICP-AES, XRD, SEM, N2 adsorption/desorption, and VSM. It was identified that the chemical composition had a significant influence on the physicochemical characteristics of MnxFe3−xO4 samples. The specimen with value of x=1.07 (Mn1.07Fe1.93O4) exhibited a unique combination of good monodispersity, regular morphology (sphere-like), abundant porosity, uniform size, distinct crystalline structure, satisfactory water dispersability, and high magnetic responsivity. Activities of these magnetically recoverable MnxFe3−xO4 samples were evaluated by employing them as Fenton catalysts for the degradation of highly concentrated methylene blue (MB, 400mg·L−1). Exceptionally high activity for the catalytic degradation of MB without any external energy input was achieved, being 1–2 orders of magnitudes greater than that over other Fe-based or Mn-based heterogeneous catalysts. We demonstrated that the large surface area of MnxFe3−xO4 as well as the high activity and favorable regeneration of the Mn2+ sites were responsible for the excellent performance. Overall, this study provides not only a practical strategy for rational design of targeted spinel-type ferrite nanomaterials, but also a new physical insight on catalytic activity of manganese ferrite and its application to organic pollutant removal.

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.