Effect of calcination atmosphere on the structure and photocatalytic properties of titania mesoporous powder

Effect of calcination atmosphere on the structure and photocatalytic properties of titania... In the work presented here, mesoporous titania (MTO) powders are synthesised by the sol–gel method using amphiphilic triblock copolymer as a template in two different calcination atmospheres, N2 and air. Various techniques such as sequential thermal analysis (STA), small-angle X-ray diffraction (SAXRD), wide-angle X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), ultraviolet (UV)–visible spectroscopy, high-resolution transmission electron microscopy (HRTEM) and N2-adsorption/desorption analysis were utilised to study the prepared samples. Furthermore, the photocatalytic activities of the prepared samples were evaluated from the photo-degradation analysis of methylene blue (MB). For the sample calcined at N2, the formation of an ordered mesostructure with a high specific surface area (172 m2 g−1), mesoporosity (48%) and enhanced photocatalytic activity were obtained compared to that of the sample calcined in air. The observed increased MB degradation for the latter is mainly attributed to the formation of higher specific surface area and mesoporosity. The availability of highly ordered open-pore channels could provide increased contacts between reactants in the solution and the active sites on the surface of titania mesoporous particles. Considering the photoactivities of the samples, it is revealed that the photocatalytic activity is enhanced, together with an increase in the surface defects in N2 atmosphere. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Research on Chemical Intermediates Springer Journals

Effect of calcination atmosphere on the structure and photocatalytic properties of titania mesoporous powder

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Publisher
Springer Netherlands
Copyright
Copyright © 2012 by Springer Science+Business Media B.V.
Subject
Chemistry; Inorganic Chemistry; Catalysis; Physical Chemistry
ISSN
0922-6168
eISSN
1568-5675
D.O.I.
10.1007/s11164-011-0477-6
Publisher site
See Article on Publisher Site

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