4.7 Article

Sol-gel synthesis of photoactive zirconia-titania from metal salts and investigation of their photocatalytic properties in the photodegradation of methylene blue

Journal

POWDER TECHNOLOGY
Volume 258, Issue -, Pages 99-109

Publisher

ELSEVIER
DOI: 10.1016/j.powtec.2014.03.024

Keywords

Zirconia-titania; Sol-gel process; TiOCl2; Zirconyl nitrate; Photodegradation

Funding

  1. Korea Institute of Energy Technology Evaluation and Planning (KETEP) from the Ministry of Trade, Industry and Energy, Korea [20124030200130]

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Photoactive metal oxide systems capable of reducing non-biodegradable pollutants are highly needed heterogeneous catalysts for environmental purification. Most of the currently available heterogeneous catalysts are obtained from complicated synthetic routes using expensive and perhaps hazardous precursors. The present study reports a novel sol-gel method to synthesize pure TiO2 and ZrO2-TiO2 samples using titanium oxychloride as TiO2 precursor and zirconyl nitrate hydrate as a ZrO2 source in the presence of the surfactant. The ratio of Zr-to-Ti was controlled between 0.75 and 3.2 to evaluate the effect of the amount of ZrO2 in the composites. Consequently, the precipitates were calcined at different temperatures to investigate the effect of removing the template at different sintering temperatures. The physico-chemical properties of the samples were examined by SEM, HRTEM, DT-TGA, XRD, FTIR, XRF, EDX, nitrogen gas physisorption and UV-visible diffusive reflectance spectrometry analyses. These analyses revealed that the crystallization, dispersion, particle size and shape of the samples are critically dependent upon the calcination temperatures and Zr-to-Ti ratios. Abnormal grain growth (AGG) was unexpectedly observed in the samples calcined at higher temperatures (<= 800 degrees C). Comparisons of the activities of the samples toward decolorization of methylene blue indicated that the photocatalytic efficiencies of the composites with Zr/ri <= 2.2 were superior to that of pure TiO2. (C) 2014 Elsevier B.V. All rights reserved.

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