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Copyright (c) 2014 Ahmed Belhakem1, Samia A. Ghomari2, Fawzi Taleb1
This work is licensed under a Creative Commons Attribution 4.0 International License.
Carbon Monoxide Conversion Using Functionalized Clay Material with Ptn+, H+ and (Ptn+/H+) Cations
Corresponding Author(s) : Ahmed Belhakem1
Asian Journal of Chemistry,
Vol. 26 No. 20 (2014)
Abstract
Sodium acetate intercalated halloysites, functionalized with Ptn+, H+ and (Ptn+/H+) cations, were used as catalysts in the carbon monoxide conversion reaction. Experiments were carried out at 3.5 103 torr, 523 K and H2/CO ratio (about 2) or (H2/CO = 67 %/33 % v/v). Platinum ionic species, their distribution and average size particle were determined by X-Ray absorption near edge structure (XANES) and titration of adsorbed H2 by O2 techniques, respectively. The obtained results showed that CO conversions were higher with (Ptn+/H+) than with H+ or Ptn+ cations used as catalysts. These results were in accordance with the fact that H+ and Ptn+ combination generates a higher level of acidity. The activation/deactivation process showed that catalysts could be easily regenerated after each reaction by heating at 250 °C for 5 h. For the present study, a higher selectivity toward light hydrocarbons (C1-C4) was noticed. The catalysts nature, structure and texture played a major role on the quality and quantity of the final products.
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M. Alkan and M. Dogan, J. Colloid Interf. Sci., 243, 280 (2001).
J.C.Y. Ng, W.H. Cheung and G. McKay, J. Colloid Interf. Sci., 255, 64 (2002).
S. Rengaraj, Y. Kim, C.K. Joo and J. Yi, J. Colloid Interf. Sci., 273, 14 (2004).
M. Arias, C. Pérez-Novo, F. Osorio, E. López and B. Soto, J. Colloid Interf. Sci., 288, 21 (2005).
M. Seredych and T. Bandosz, J. Colloid Interf. Sci., 302, 379 (2006).
X. Gu and J.L. Evans, J. Colloid Interf. Sci., 307, 317 (2007).
K.G. Bhattacharyya and S.S. Gupta, Sep. Purif. Technol., 50, 388 (2006).
A. Li and J. Dai, Water Res., 40, 1951 (2006).
J. Hizal and A.R. Apak, J. Colloid Interf. Sci., 295, 1 (2006).
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J. Panpranot, J.G. Goodwin Jr. and A. Sayari, J. Catal., 213, 78 (2003).
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A. Corma and H. Garcia, Chem. Rev., 103, 4307 (2003).
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W.E. Farneth and R.J. Gorte, Chem. Rev., 95, 615 (1995).
J. Zhuang, D. Ma, Z. Yan, X. Liu, X. Han, X. Bao, Y. Zhang, X. Guo and X. Wang, Appl. Catal. A, 258, 1 (2004).
J.F. Haw, Phys. Chem. Chem. Phys., 4, 5431 (2002).
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M. Johns, P. Landon, T. Alderson and G.J. Hutchings, Chem. Commun., 23, 2454 (2001).
M. Xiang, J. Zou, Q. Li and X. She, J. Nat. Gas Chem., 19, 468 (2010).
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M. Johns, P. Collier, M.S. Spencer, A. Alderson and G.J. Hutchings, Catal. Lett., 90, 187 (2003).
T. Sakakura, J.-C. Choi and H. Yasuda, Chem. Rev., 107, 2365 (2007).
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B. Enderle and B. Gates, J. Mol. Catal. Chem., 204-205, 473 (2003).
C.E. Hédoire, C. Louis, A. Davidson, M. Breysse, F. Maugé and M. Vrinat, J. Catal., 220, 433 (2003).
H. Yang, H. Chen, J. Chen, O. Omotoso and Z. Ring, J. Catal., 243, 36 (2006).
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C. Jones, S.H. Taylor, A. Burrows, M.J. Crudace, C.J. Kiely and G.J. Hutchings, Chem. Commun., 14, 1707 (2008).
Á. Mastalir, B. Rác, Z. Király and Á. Molnár, J. Mol. Catal. Chem., 264, 170 (2007).
G. Crépeau, V. Montouillout, A. Vimont, L. Mariey, T. Cseri and F. Maugé, J. Phys. Chem. B, 110, 15172 (2006).