Oxidative Dehydrogenation of Cyclohexane over Mg-V-O Catalysts Prepared via Citriate Complexation

Article Preview

Abstract:

Oxidative dehydrogenation of cyclohexane was studied over three pure Mg-V-O catalysts, which are Mg3(VO4)2, Mg2V2O7 and MgV2O6, respectively. Catalysts were prepared via citric acid complexation and characterized by N2-adsorption, XRD, FT-IR, NH3-TPD and H2-TPR techniques. Among the pure magnesium vanadates, Mg3(VO4)2 has the isolated active sites, weakly basic surface and lower reducibility of the metal cations, and could be recognized as the catalytic active phase. Mg3(VO4)2 catalyst exhibited a better catalytic performance, on which a cyclohexene selectivity of 41.5% at cyclohexane conversion of 15.5% was obtained.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 284-286)

Pages:

692-696

Citation:

Online since:

July 2011

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2011 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] U. Schuchardt, D. Cardoso, R. Sercheli, R. Pereira, R.S. Cruz, M.C. Guerreiro, D. Mandelli, E.V. Spinace and E.L. Pires: Appl. Catal. A: General, Vol.211 (2001), p.1.

DOI: 10.1016/s0926-860x(01)00472-0

Google Scholar

[2] S.C. Liu, Z.Y. Liu, Z. Wang, Y.M. Wang and P. Yuan: J. Chem. Eng. , Vol.139 (2008), p.157.

Google Scholar

[3] M. Riad and S. Mikhail: Catal. Comm., Vol.9 (2008), p.1398.

Google Scholar

[4] H. Zhu, Q.J. Ge, W.Z. Li, X.B. Liu and H.Y. Xu: Catal. Lett., Vol.105 (2005), p.29.

Google Scholar

[5] A. Klisińska, K. Samson, I. Gressel and B. Grzybowska: Appl. Catal. A: General, Vol. 309 (2006), p.10.

Google Scholar

[6] S. Blanco, S.R.G. Carrazán and V. Rives: Appl. Catal. A: General, Vol.342 (2008), p.93.

Google Scholar

[7] M.A. Charr, D. Patel, M.C. Kung and H.H. Kung: J. Catal., Vol.105 (1987), p.483.

Google Scholar

[8] D. Patel, M.C. Kung and H.H. Kung: Chem. Institute of Canada 4 (1988), p.1553.

Google Scholar

[9] M.A. Chaar, D. Patel and H.H. Kung: J. Catal., Vol.109 (1988), p.463.

Google Scholar

[10] D.S.H. Sam, V. Soenen and J.C. Volta: J.Catal., Vol.123(1990), p.417.

Google Scholar

[11] M.C. Kung and H.H. Kung: J. Catal., Vol.128 (1991), p.287.

Google Scholar

[12] M.Jin, Z. M.Cheng, Y. L.Gao and X. C. Fang: Mater. Lett., Vol.63 (2009), p.2055.

Google Scholar

[13] J. Hanuza, B. Jerowska-Trzebiatowska and W. Oganowski: J. Mol. Catal., Vol.29 (1985), p.109.

Google Scholar

[14] D.S.H. Sam, V. Soenen and J.C. Volta: J. Catal. , Vol.123 (1990), p.417.

Google Scholar

[15] X.T. Gao, P. Ruiz, Q. Xin, X.X. Guo and B. Delmon: J. Catal., Vol.148 (1994), p.56.

Google Scholar

[16] L. Balderas-Tapia, I. Hernández-Pérez, P. Schacht, L.R. Córdova and G.G. Aguilar-Ríos: Catal. Today, Vol.107-108 (2005), p.371.

DOI: 10.1016/j.cattod.2005.07.025

Google Scholar

[17] P. Mars and D.W. Van Krevenlen: Chem. Eng. Sci.( Suppl.), Vol.3 (1954), p.341.

Google Scholar

[18] H. N. Ng and C.Calvo: J Canad Chem, Vol.50 (1972), p.3619.

Google Scholar

[19] G. M. Clark and R. J.Morley: Solid State Chem., Vol.16 (1976), p.429.

Google Scholar

[20] R.K. Grasselli, Topics in Catal., Vol.21 (2002), p.79.

Google Scholar

[21] M.P. Casaletto, L. Lisi, G. Mattogno, P. Patrono, G. Ruoppolo and G. Russo: Appl. Catal. A: General, Vol.226 (2002), p.41.

Google Scholar

[22] S. Sugiyama, T. Osaka, Y. Hirata and K.I. Sotowa: Appl. Catal. A: General, Vol.312 (2006), p.52.

Google Scholar