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Effect of Preparation Conditions on the Hydrogenation Activity and Metal Dispersion of Pt/C and Pd/C Catalysts

  • Jhung, Sung-Hwa (Research Center for Nanocatalysts, Korea Research Institute of Chemical Technology) ;
  • Lee, Jin-Ho (Research Center for Nanocatalysts, Korea Research Institute of Chemical Technology) ;
  • Lee, Jong-Min (Research Center for Nanocatalysts, Korea Research Institute of Chemical Technology) ;
  • Lee, Ji-Hye (Research Center for Nanocatalysts, Korea Research Institute of Chemical Technology) ;
  • Hong, Do-Young (Research Center for Nanocatalysts, Korea Research Institute of Chemical Technology) ;
  • Kim, Myong-Woon (DNF Solution Co.) ;
  • Chang, Jong-San (Research Center for Nanocatalysts, Korea Research Institute of Chemical Technology)
  • Published : 2005.04.20

Abstract

The Pt/C and Pd/C catalysts were prepared from conventional chloride precursors by adsorption or precipitation-deposition methods. Their activities for hydrogenation reactions of cyclohexene and acetophenone were compared with those of commercial catalysts. The Pt/C and Pd/C catalysts obtained from the adsorption procedure reveal higher hydrogenation activity than commercial catalysts and the catalysts prepared by the precipitation-deposition method. Their improved performances are attributed to the decreased metal crystallite sizes of Pt or Pd formed on the active carbon support upon the adsorption of the precursors probably due to the same negative charges of the chloride precursor and the carbon support. Under the preparation conditions studied, the reduction of the supported catalysts using borohydrides in liquid phase is superior to a gas phase reduction by using hydrogen in the viewpoint of particle size, hydrogenation activity and convenience.

Keywords

References

  1. Seldon, R. A.; van Bekkum, H. Fine Chemicals through Heterogeneous Catalysis; Wiley-VCH: Weinheim, 2001
  2. Simonov, P. A.; Likholobov, V. A. In Catalysis and Electrocatalysis at Nanoparticle Surfaces; Wieckowski, A.; Savinova, E. R.; Vayenas, C. G., Eds.; Marcel Dekker: New York, 2003; pp 409-454
  3. Auer, E.; Freund, A.; Pietsch, J.; Tacke, T. Appl. Catal. A 1998, 173, 259 https://doi.org/10.1016/S0926-860X(98)00184-7
  4. Shen, K.; Li, S.; Choi, D. H. Bull. Kor. Chem. Soc. 2002, 23, 1785 https://doi.org/10.5012/bkcs.2002.23.12.1785
  5. Okhlopkova, L. B.; Lisitsyn, A. S.; Likholobov, V. A.; Gurrath, M.; Boehm, H. P. Appl. Catal. A 2000, 204, 229 https://doi.org/10.1016/S0926-860X(00)00534-2
  6. Gurrath, M.; Kuretzky, T.; Boehm, H. P.; Okhlopkova, L. B.; Lisitsyn, A. S.; Likholobov, V. A. Carbon 2000, 38, 1241
  7. Rodriguez-Reinoso, F. Carbon 1998, 36, 159 https://doi.org/10.1016/S0008-6223(97)00173-5
  8. Kim, S.-C.; Park, H.-H.; Lee, D.-K. Catal. Today 2003, 87, 51 https://doi.org/10.1016/j.cattod.2003.10.008
  9. Noh, J.; Yang, O.-B.; Kim, D. H.; Woo, S. I. Catal. Today 1999, 53, 575 https://doi.org/10.1016/S0920-5861(99)00145-5
  10. Kim, W. B.; Park, E. D.; Lee, J. S. Appl. Catal. A 2003, 242, 335 https://doi.org/10.1016/S0926-860X(02)00545-8
  11. Kim, W. B.; Park, E. D.; Lee. C. W.; Lee, J. S. J. Catal. 2003, 218, 334 https://doi.org/10.1016/S0021-9517(03)00089-7
  12. Jhung, S. H.; Romanenko, A. V.; Lee, K. H.; Park, Y.-S.; Moroz, E. A.; Likholobov, V. A. Appl. Catal. A 2002, 225, 131 https://doi.org/10.1016/S0926-860X(01)00853-5
  13. Romanenko, A. V.; Tyschishin, E. A.; Moroz, E. A.; Likholobov, V. A.; Zaikovskii, V. I.; Jhung, S. H.; Park, Y.-S. Appl. Catal. A 2002, 227, 117 https://doi.org/10.1016/S0926-860X(01)00928-0
  14. Jhung, S. H.; Park, Y.-S. J. Korean Chem. Soc. 2002, 46, 57 https://doi.org/10.5012/jkcs.2002.46.1.057
  15. Suh, D. J.; Park, T.-J.; Ihm, S.-K. Ind. Eng. Chem. Res. 1992, 31, 1849 https://doi.org/10.1021/ie00008a003
  16. Romanenko, A. V.; Likholobov, V. A.; Timofeeva, M. N.; Jhung, S. H.; Park, Y.-S. U S Patent 2004, 6 753 290
  17. Prabhuram, J.; Zhao, T. S.; Wong, C. W.; Guo, J. W. J. Power Sources 2004, 134, 1 https://doi.org/10.1016/j.jpowsour.2004.02.021
  18. Mao, S. S.; Mao, G. U S Patent 2004, 6 686 308
  19. Wu, S. F.; Yanagisawa, K.; Nishizawa, T. Carbon 2001, 39, 1537 https://doi.org/10.1016/S0008-6223(00)00275-X
  20. Kung, H. H.; Kung, M. C.; Costello, C. K. J. Catal. 2003, 216, 425 https://doi.org/10.1016/S0021-9517(02)00111-2
  21. Semikolenov, V. A.; Lavrenko, S. P.; Zaikovskii, V. I. React. Kinet. Catal. Lett. 1993, 51, 507 https://doi.org/10.1007/BF02069098
  22. Chen, C.-S.; Chen, H.-W.; Cheng, W.-H. Appl. Catal. A 2003, 248, 117 https://doi.org/10.1016/S0926-860X(03)00156-X

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