Author:
Mei Congwei,Yuan Yinnan,Li Xianming,Mei Deqing
Abstract
The MoO3 catalysts supported on nano-scale TiO2 with various loading rates (5%, 10%, 20%, and 40%) were prepared by an impregnation method. The phase structures of nano-scale MoO3/TiO2 catalysts were characterized by Brunner-Emmet-Teller, Fourier Transform Infrared Spectra, X-ray Diffraction, and Scanning Electron Microscope. The oxidation activities of catalysts over diesel soot were performed in a Thermogravimetric Analysis system. The kinetics of the catalytic oxidation process was analyzed based on Starink method. The characterization results showed that the phase structure of MoO3 supported on TiO2 depends heavily on the molybdenum contents, which put great effects on soot oxidation. The orthorhombic crystal system (α-MoO3) appeared on the surface of the catalysts when the MoO3 exceeds 10%. Due to the low melting point and good surface mobility of MoO3, the catalytic activity was increased and the characteristic temperatures were decreased with the increase in MoO3 contents. As a result, the activities of catalysts with different loading rates for soot oxidation can be ranked as: Mo5<Mo10<Mo20<Mo40. Via pyrolysis kinetics analysis, it is revealed that Mo40 requires the minimum activation energy for soot oxidation, which fits well with the TG experimental results. In summary, the catalytic activity of MoO3 breaks the threshold effect. Copyright © 2016 BCREC GROUP. All rights reserved <br /> <em>Received: 19th July 2016; Revised: 30th August 2016; Accepted: 9th September 2016</em> <br /> <strong>How to Cite:</strong> Mei, C., Yuan, Y., Li, X., Mei, D. (2016). Microscopic Phase Structure of Mo-based Catalyst and Its Catalytic Activity for Soot Oxidation. <em>Bulletin of Chemical Reaction Engineering & Catalysis</em>, 11 (3): 389-397 (doi:10.9767/bcrec.11.3.608.389-397) <br /> <strong>Permalink/DOI:</strong> <a href="http://doi.org/10.9767/bcrec.11.3.608.389-397" />http://doi.org/10.9767/bcrec.11.3.608.389-397</a>
Publisher
Bulletin of Chemical Reaction Engineering and Catalysis
Subject
Process Chemistry and Technology,Catalysis
Cited by
2 articles.
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