화학공학소재연구정보센터
Korean Journal of Chemical Engineering, Vol.14, No.1, 49-58, January, 1997
EFFECT OF IRON ON Cu/SiO2 CATALYSTS FOR THE DEHYDROGENATION OF CYCLOHEXANOL TO CYCLOHEXANONE
At the temperature range of 250-390℃, the addition of iron to Cu/SiO2 catalyst increased the conversion and the selectivity of cyclohexanone. The iron incorporation into Cu/SiO2 catalyst enhanced the reduction temperature of copper oxide, increased the dispersion of copper metal and decreased the selectivity of cyclohexene. Copper was enriched on the surface of the used metal catalyst compared to that in freshly calcined or reduced catalyst. Unlike Cu dispersed on bulk iron oxide, the Cu-Fe dispersed on silica showed negligible amount of phenol formation, thus keeping the selectivity of cyclohexanone very high even at high reaction temperatures. The Fe3+ ion in the reduced Cu/Fe/SiO2 catalyst resulted in a significant resistance of the Cu particle to sintering and a decrease in the selectivity of phenol arisen from the magnetite.
  1. Anderson JR, "Structure of Metallic Catlaysts," Academic Press, London (1975)
  2. Boyce AL, Graville SR, Sermon PA, Vong MSW, React. Kinet. Catal. Lett., 44, 13 (1991) 
  3. Charcosset H, Delmon B, Ind. Chim. Belg, 38, 481 (1973)
  4. Charcosset H, Frety R, Soldot A, Trambouze Y, J. Catal., 22, 204 (1971) 
  5. Chen WS, Lee MD, Lee JF, Appl. Catal. A: Gen., 83, 201 (1992) 
  6. Chinchen GC, Hay CM, Vandervell HD, Waugh KC, J. Catal., 103, 79 (1987) 
  7. Cubberley AH, Mueller MB, J. Am. Chem. Soc., June, 1535 (1947)
  8. Dowden DA, Endeavour, 24, 69 (1965) 
  9. Emelyanov NP, Bel'skaya RI, Semyachko RY, "Catalyst for Cyclohexanol Dehydrogenation to Cyclohexanone," U.S. Patent, 3,652,460 (1972)
  10. Fridman VZ, Bedina LN, Petrov IY, Kinet. Katal., 29, 621 (1988)
  11. Gentry SJ, Hurst NW, Jones A, J. Chem. Soc.-Faraday Trans., 77, 603 (1981) 
  12. Haber J, Machej T, Ungier L, Ziokkowski J, J. Solid State Chem., 25, 207 (1978) 
  13. Hino M, Arata K, Chem. Lett., 1737 (1990) 
  14. Jeon GS, Chung JS, Korean J. Chem. Eng., 12(1), 132 (1995)
  15. Jeon GS, Chung JS, Korean J. Chem. Eng., to submitted (1996)
  16. Jeon GS, Chung JS, Appl. Catal. A: Gen., 115(1), 29 (1994) 
  17. Klier K, Adv. Catal., 31, 243 (1982)
  18. Kobayashi H, Takezawa N, Minochi C, J. Catal., 69, 487 (1981) 
  19. Kohler MA, Wainwright MS, Trimm DL, Cant NW, Ind. Eng. Chem. Prod. Res. Dev., 26, 652 (1987)
  20. Komarov VS, Bel'skaya RI, Skruko OF, Taborissakaya EA, "Catalyst for Dehydrogenation of Cyclohexanol to Cyclohexanone," U.S.S.R. Patent, 411 888 (1974)
  21. Lin YM, Wang I, Yeh CT, Appl. Catal., 41, 53 (1988) 
  22. Minochi C, Kobayashi H, Takezawa N, Chem. Lett., 507 (1979) 
  23. Monti DM, Wainwright MS, Trimm DL, Cant NW, Ind. Eng. Chem. Prod. Res. Dev., 24, 397 (1985) 
  24. Parris GE, Klier K, J. Catal., 97, 374 (1986) 
  25. Rachel A, Sivaraj C, Reddy GK, Vijayakumar V, Rao PK, Ind. J. Chem., 32A, 857 (1993)
  26. Schon G, Surf. Sci., 35, 96 (1973) 
  27. Sermon PA, Bond GC, Catal. Rev.-Sci. Eng., 8, 211 (1974)
  28. Sivaraj C, Reddy BM, Rao PK, Appl. Catal., 45, L11 (1988) 
  29. Sivaraj C, Srinvas ST, Rao VN, Rao PK, J. Mol. Catal., 60, L23 (1990) 
  30. Sodesawa T, React. Kinet. Catal. Lett., 24, 259 (1984) 
  31. Sodesawa T, Nagacho M, Onodera A, Nozaki F, J. Catal., 102, 460 (1986) 
  32. Uemichi Y, Sakai T, Kanazuka T, Chem. Lett., 777 (1989) 
  33. Wagner CD, Riggs WH, Davis LE, Mullenberg GE, "Handbook of X-ray Photoelectron Spectroscopy," Perkin-Elmer Co., Minnesota
  34. Wang I, Lin YM, "Method of Producing Cyclohexanone from Cyclohexanol through Oxidative Dehydrogenation," U.S. Patent, 4,198,239 (1990)
  35. Yin L, Adler I, Tsang T, Matienzo LJ, Grim SO, Chem. Phys. Lett., 24, 81 (1974)