Photocatalytic Degradation of Methylene Blue Dye Using TiO2 and Fe3O4/SiO2/TiO2 as Photocatalysts
This paper is focused on obtained two catalysts such as TiO2 nanoparticles and Fe3O4/SiO2/TiO2 nanocomposite for adsorption and photocatalytic degradation of methylene blue (MB) dyes from aqueous solution. The morphology, structure and chemical proprieties of synthesized materials were investigated...
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Veröffentlicht in: | IOP conference series. Materials Science and Engineering 2020-06, Vol.877 (1) |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | This paper is focused on obtained two catalysts such as TiO2 nanoparticles and Fe3O4/SiO2/TiO2 nanocomposite for adsorption and photocatalytic degradation of methylene blue (MB) dyes from aqueous solution. The morphology, structure and chemical proprieties of synthesized materials were investigated by X-ray diffraction (XRD) analysis, scanning electron microscopy (SEM), N2 adsorption-desorption isotherms and Zeta potential. The photocatalytic degradation of methylene blue under UV light in the presence of different synthesized catalysts was analyzed with Spectrometer UV-Vis. The photocatalytic degradation of methylene blue was studies by focusing of photoactivity performance of Fe3O4/SiO2/TiO2 in comparation with TiO2. An attempt has been made to study the effect of process parameters through amount of the catalysts and initial concentrations of methylene blue. In all cases was found that the kinetics of the MB photocatalytic degradation under UV light was fitted to the Langmuir-Hinshelwood. Even if the photocatalytic degradation study revealed that Fe3O4/SiO2/TiO2 and TiO2 degraded about 90 % of methylene blue within 60 min, the magnetic nanocomposite Fe3O4/SiO2/TiO2 serves as better catalyst compared with TiO2 nanoparticles. An important role in the photocatalytic degradation of MB is adsorption characteristic of TiO2 and Fe3O4/SiO2/TiO2 surface. The photocatalytic performance of Fe3O4/SiO2/TiO2 remained greater than TiO2 after 4 cycles of use. |
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ISSN: | 1757-8981 1757-899X |
DOI: | 10.1088/1757-899X/877/1/012008 |