Photocatalytic degradation of phenol by visible light-responsive iron-doped TiO"2 and spontaneous sedimentation of the TiO"2 particles [An article from: Chemosphere]
Book Details
Author(s)Mst.S. Nahar, K. Hasegawa, S. Kagaya
PublisherElsevier
ISBN / ASINB000PC05K8
ISBN-13978B000PC05K7
AvailabilityAvailable for download now
Sales Rank99,999,999
MarketplaceUnited States 🇺🇸
Description
This digital document is a journal article from Chemosphere, published by Elsevier in 2006. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
Fe-doped TiO"2 was prepared by the calcination of Fe"xTiS"2 (x=0, 0.002, 0.005, 0.008, 0.01) and characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV-visible diffuse reflectance spectra. All the Fe-doped TiO"2 were composed of an anatase crystal form and showed red shifts to a longer wavelength. The activity of the Fe-doped TiO"2 for the degradation of phenol was investigated by varying the iron content during UV (365nm) and visible light (405nm and 436nm) irradiation. The degradation rate depended on the Fe content and the Fe-doped TiO"2 was responsive to the visible light as well as the elevated activity toward UV light. The molar ratio of 0.005 was the optimum for both the UV and visible light irradiations. The result was discussed on the basis of the balance of the excited electron-hole trap by the doped Fe^3^+ and their charge recombination on the doped Fe^3^+ level. The Fe-doped TiO"2 (x=0.005) was more active than P25 TiO"2 under solar light irradiation. The suspended Fe-doped TiO"2 spontaneously precipitated once the stirring of the reaction mixture was terminated.
Description:
Fe-doped TiO"2 was prepared by the calcination of Fe"xTiS"2 (x=0, 0.002, 0.005, 0.008, 0.01) and characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and UV-visible diffuse reflectance spectra. All the Fe-doped TiO"2 were composed of an anatase crystal form and showed red shifts to a longer wavelength. The activity of the Fe-doped TiO"2 for the degradation of phenol was investigated by varying the iron content during UV (365nm) and visible light (405nm and 436nm) irradiation. The degradation rate depended on the Fe content and the Fe-doped TiO"2 was responsive to the visible light as well as the elevated activity toward UV light. The molar ratio of 0.005 was the optimum for both the UV and visible light irradiations. The result was discussed on the basis of the balance of the excited electron-hole trap by the doped Fe^3^+ and their charge recombination on the doped Fe^3^+ level. The Fe-doped TiO"2 (x=0.005) was more active than P25 TiO"2 under solar light irradiation. The suspended Fe-doped TiO"2 spontaneously precipitated once the stirring of the reaction mixture was terminated.
