Fabrication of porous Fe2O3/PTFE nanofiber membranes and their application as a catalyst for dye degradationElectronic supplementary information (ESI) available. See DOI: 10.1039/c5ra27879a

Novel porous polytetrafluoroethylene (PTFE) nanofiber membranes containing Fe 2 O 3 (Fe 2 O 3 /PTFE), used as a heterogeneous catalyst, were prepared via a three-step method by electrospinning, immersion and calcination. The morphology and structure of porous Fe 2 O 3 /PTFE were characterized by sca...

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Main Authors Kang, Weimin, Li, Fu, Zhao, Yixia, Qiao, Chunmei, Ju, Jingge, Cheng, Bowen
Format Journal Article
Published 04.04.2016
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Summary:Novel porous polytetrafluoroethylene (PTFE) nanofiber membranes containing Fe 2 O 3 (Fe 2 O 3 /PTFE), used as a heterogeneous catalyst, were prepared via a three-step method by electrospinning, immersion and calcination. The morphology and structure of porous Fe 2 O 3 /PTFE were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS) and X-ray diffractometer (XRD). The effects of the thickness of the as-spun nanofiber membrane, the immersion time and impregnating solution concentration on the content of Fe 2 O 3 which was the active component were discussed. The degradation of Acid Red with hydrogen peroxide catalyzed by the porous Fe 2 O 3 /PTFE under UV irradiation was investigated. UV-vis and ESR techniques provided an insight into the nature of the degradation products and the formed active species. The results showed that Fe 2 O 3 was successfully supported on the surface of porous PTFE nanofibers. The porous Fe 2 O 3 /PTFE nanofiber membrane prepared under the optimized parameters possessed high photocatalytic activity without any dye adsorption and could be recycled by simple filtration. Novel porous polytetrafluoroethylene (PTFE) nanofiber membranes containing Fe 2 O 3 (Fe 2 O 3 /PTFE), used as a heterogeneous catalyst, were prepared via a three-step method by electrospinning, immersion and calcination.
Bibliography:10.1039/c5ra27879a
Electronic supplementary information (ESI) available. See DOI
ISSN:2046-2069
DOI:10.1039/c5ra27879a