Ammoxidation of 3-Picoline over V2O5/TiO2 Catalysts: Effects of TiO2 Supports on the Catalytic Performance

Article Preview

Abstract:

A series of V2O5/TiO2 catalysts were prepared by wet impregnation, and these prepared catalysts were characterized by XRD, N2 adsorption-desorption, H2-TPR, and TEM techniques and used in the selective ammoxidation of 3-picoline to 3-cyanopyridine. The effects of TiO2 supports on the catalytic properties of the resulting catalysts for the ammoxidation of 3-picoline to 3-cyanopyridine were investigated in detail. It is found that the V5+/V4+ transformation during ammoxidation is more favorable than the V5+/V3+ transformation for the selective ammoxidation of 3-picoline to 3-cyanopyridine. The V2O5/TiO2 catalysts prepared from the nanosized TiO2 particles as supports show a high activity for the direct oxidation of 3-picoline by air, resulting Subscript text Subscript textin a low selectivity for 3-cyanopyridine. This could be due to the fact that the active species vanadium oxides could be only supported on the external surface of the nano-sized TiO2 particles with very minor contact area, leading to the weak interactions between active species and support.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 396-398)

Pages:

791-797

Citation:

Online since:

November 2011

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2012 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] R. Yokoyama and K. Sawada, D.E Patent 1940320. (1971)

Google Scholar

[2] A. Andersson and S.T. Lundin: J. Catal. Vol. 58 (1979), p.383

Google Scholar

[3] A. Baiker and P. Zollinger: Appl. Catal. Vol. 10 (1984), p.231

Google Scholar

[4] A. Andersson: J. Catal. Vol. 69 (1981), p.465

Google Scholar

[5] A. Andersson and S.T. Lundin: J. Catal. Vol. 65 (1980), p.9

Google Scholar

[6] A. Andersson: J. Catal. Vol. 76 (1982), p.144

Google Scholar

[7] A. Andersson and S.L.T. Andersson: ACS Symp. Ser. Vol. 279 (1985), p.121

Google Scholar

[8] K.V. Narayana, A. Venugopal, K.S.R. Rao, V.V. Rao, S.K. Masthan and P.K. Rao. Appl. Catal. A Vol. 150 (1997), p.269

Google Scholar

[9] K.V. Narayana, A. Venugopal, K.S.R. Rao, S.K. Masthan, V.V. Rao and P.K. Rao: Appl. Catal. A Vol. 167 (1998), p.11

Google Scholar

[10] G.C. Bond, J.P. Zurita, S. Flamerz, P.J. Gellings, H. Bosch, J.G. Vanommen and B.J. Kip: Appl. Catal. Vol. 22 (1986), p.361

Google Scholar

[11] G.C. Bond, S. Flamerz and R. Shukri: Faraday Discuss. Chem. Soc. Vol. 87 (1989), p.65

DOI: 10.1039/dc9898700065

Google Scholar

[12] G.C. Bond and S.F. Tahir: Appl. Catal. Vol. 71 (1991), p.1

Google Scholar

[13] K.V.R. Chary, G. Kishan, K. Lakshmi and K. Ramesh: Langmuir Vol. 16 (2000), p.7192

Google Scholar

[14] K.V.R. Chary, G. Kishan, T. Bhaskar and H. Sivaraj: J. Phys. Chem B Vol. 102 (1998), p.6792

Google Scholar

[15] M. Sanati, A. Andersson, L.R. Wallenberg and B. Rebenstorf: Appl. Catal. A Vol. 106 (1993), p.51

Google Scholar

[16] L. Makedonski, V. Nikolov, N. Nikolov and V. Blaskov: React. Kinet. Catal. Lett. Vol. 66 (1999), p.237

DOI: 10.1007/bf02475796

Google Scholar

[17] K.V. Narayana, S.K. Masthan, V.V. Rao, B.D. Raju and P.K. Rao: Catal. Commun. Vol. 3 (2002), p.173

Google Scholar

[18] K.V. Narayana, B.D. Raju, S.K. Masthan, V.V. Rao, P.K. Rao, R. Subrahmanian and A. Martin: Catal. Commun. Vol. 5 (2004), p.457

Google Scholar

[19] V.N. Kalevaru, B.D. Raju, V.V. Rao and A. Martin: Appl. Catal. A Vol. 352 (2009), p.223

Google Scholar

[20] K.V. Narayana, B.D. Raju, S.K. Masthan, V.V. Rao, P.K. Rao and A. Martin: J. Mol. Catal. A Vol. 223 (2004), p.321

Google Scholar

[21] K.V. Narayana, B.D. Raju, S.K. Masthan, V.V. Rao and P.K. Rao: Catal. Lett. Vol. 84 (2002), p.27

Google Scholar

[22] C. Janke, M. Schneider, U. Bentrup, J. Radnik, A. Martin, G. Scholz and A. Bruckner: J. Catal. Vol. 277 (2011), p.196

Google Scholar

[23] V.N. Kalevaru, N. Madaan and A. Martin: Appl. Catal. A Vol. 391 (2011), p.52

Google Scholar

[24] G.C. Bond: Appl. Catal. A Vol. 157 (1997), p.91

Google Scholar

[25] I.E. Wachs and B.M. Weckhuysen: Appl. Catal. A Vol. 157 (1997), p.67

Google Scholar

[26] G. Centi: Appl. Catal. A Vol. 147 (1996), p.267

Google Scholar

[27] I.E. Wachs: J. Catal. Vol. 124 (1990), p.570

Google Scholar

[28] C.B. Wang, G. Deo and I.E. Wachs: J Catal. Vol. 178 (1998), p.640

Google Scholar

[29] J.M. Jehng, G. Deo, B.M. Weckhuysen and I.E. Wachs: J. Mol. Catal. A Vol. 110 (19961), p.41

Google Scholar

[30] C. Cristiani, P. Forzatti and G. Busca: J. Catal. Vol. 116 (1989), p.586

Google Scholar

[31] J.X. Peng and S.D. Wang: J. Phys. Chem. C Vol. 111 (2007), p.9897

Google Scholar

[32] W.P. Huang, X.H. Tang, Y.Q. Wang, Y. Koltypin and A. Gedanken: Chem. Commun. (2000), p.1415

Google Scholar