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Effect of calcination temperature on the H2O2 decomposition activity of nano-crystalline Co3O4 prepared by combustion method

[Display omitted] ► Spinel Co3O4 nano-particles were synthesized by combustion method using urea as a combustion fuel. ► The estimated particle size using both XRD and TEM were in the range 8–34nm depending upon calcination temperature. ► The H2O2 decomposition over Co3O4 nano-particles was found to...

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Bibliographic Details
Published in:Applied surface science 2013-06, Vol.274, p.45-52
Main Authors: Makhlouf, M.Th, Abu-Zied, B.M., Mansoure, T.H.
Format: Article
Language:English
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Summary:[Display omitted] ► Spinel Co3O4 nano-particles were synthesized by combustion method using urea as a combustion fuel. ► The estimated particle size using both XRD and TEM were in the range 8–34nm depending upon calcination temperature. ► The H2O2 decomposition over Co3O4 nano-particles was found to decrease with the crystallites sized increase. Cobalt oxide nano-particles were prepared by combustion method using urea as a combustion fuel. The effects of calcination temperature, 350–1000°C, on the physicochemical, surface and catalytic properties of the prepared Co3O4 nano-particles were studied. The products were characterized by thermal analyses (TGA & DTA), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) techniques. Textural features of the obtained catalysts were investigated using nitrogen adsorption at −196°C. X-ray diffraction confirmed that the resulting oxide was pure single-crystalline Co3O4 nano-particles. Transmission electron microscopy indicating that, the crystallite size of Co3O4 nano-crystals was in the range of 8–34nm. The catalytic activities of prepared nano-crystalline Co3O4 catalysts were tested for H2O2 decomposition at 35–50°C temperature range. Experimental results revealed that, the catalytic decomposition of H2O2 decreases with increasing the calcination temperature. This was correlated with the observed particle size increase accompanying the calcination temperature rise.
ISSN:0169-4332
1873-5584
DOI:10.1016/j.apsusc.2013.02.075