Preliminary Study on Photocatalytic Degradation of Methyl Orange and Cr(VI) Compound System by Titania-Bearing Blast Furnace Slag

Article Preview

Abstract:

Using calcined sulfate-modified titanium-bearing blast furnace slag (STBBFS) as photocatalyst, decolorization efficiency of methyl orange (MO) in the presence of Cr(VI) were studied. The effect of solution pH on the decolorization efficiency of MO and reduction efficiency of Cr(VI) have been investigated. The results indicate that the acidic solutions are favorable for the photocatalytic oxidation of MO in the presence of Cr(VI), and the optimum pH for oxidation of MO is 1.5. The increasing of photocatalytic activities in the compound system can be attributed to five main reasons: (1) the redox reaction between Cr(VI) and MO; (2) adsorption of Cr(VI) species and dye molecule onto STBBFS surface; (3) the visible light irradiation; (4) Cr(VI) species reduced to Cr(III) by Mn2+ in STBBFS photocatalyst; (5) Moreover, the addition of Cr(VI) species able to act as electron scavengers to catalyst surface promotes the effective separation of electron-hole, and hence promote the increase of decolorization efficiency of MO and reduction efficiency of Cr(VI) in Cr(VI)-MO system under visible irradiation. UV-vis spectral analysis indicated that MO was completely mineralized in the presence of Cr(VI) after 240 min. FTIR spectral analysis showed that all these characteristic peaks of Cr(VI) and MO disappear after photoreaction, indicating the degradation of Cr(VI) and MO.

You might also be interested in these eBooks

Info:

Periodical:

Pages:

3-6

Citation:

Online since:

February 2012

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2012 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] H. Yang, X.X. Xue and L. Zuo. J. Chin. Ceram. Soc. Vol. 31 (2003), p.896.

Google Scholar

[2] H. Yang, X.X. Xue and X.W. Dong. Chin. J. Process Eng. Vol. 4 (2004), p.265.

Google Scholar

[3] H. Wang, H. Yang, X.X. Xue, et al. Chin. J. Process Eng. Vol. 10 (2010), p.1025.

Google Scholar

[4] N. Zhao, H. Yang, and X.X. Xue. J. Chin. Ceram. soc. Vol. 33 (2005), p.202.

Google Scholar

[5] X.F. Lei, X.X. Xue. Mater. Chem. Phys. Vol. 112 (2008), p.928.

Google Scholar

[6] X.X. Xue, X.F. Lei and H. Yang. J. Northeastern University Vol. 30 (2009), p.217.

Google Scholar

[7] O. Horvath, E. Bodnar and J. Hegyi. Colloids Surf. A: Physicochem. Eng. Aspects Vol. 265 (2005), p.135.

Google Scholar

[8] L.M. Wang, N. Wang, L.H. Zhu. J. Hazard Mater. Vol. 152 (2008), p.93.

Google Scholar

[9] J.K. Yang, S.M. Lee. Chemosphere Vol. 63 (2006), p.1677.

Google Scholar

[10] X.F. Lei, X.X. Xue. Acta. Chim. Sinica 66 (2008), p.2539.

Google Scholar

[11] E. Malkoc, Y. Nuhoglu. Sep. Purif. Technol. Vol. 54 (2007), p.291.

Google Scholar

[12] X.F. Lei, X.X. Xue. J. Chin. Ceram. soc. Vol. 11 (2008), p.34.

Google Scholar

[13] C.R. Chenthamarakshan, K. Rajeshwar and E. Wolfrum. Langmuir Vol. 16 (2000), p.2715.

Google Scholar

[14] T. Papadam, N.P. Xekoukoulotakis and I. Poulios. J. Photochem. Photobiol. A Vol. 186 (2007), p.308.

Google Scholar

[15] F. Jiang, Z. Zheng and Z.Y. Xu. J. Hazard Mater. Vol. 134 (2006), p.94.

Google Scholar