Issue
Korean Journal of Chemical Engineering,
Vol.23, No.6, 896-901, 2006
Kinetics of esterification of propionic acid with n-amyl alcohol in the presence of cation exchange resins
Esterifications of n-amyl alcohol with propionic acid catalyzed by macroporous (Amberlyst-15) and microporous (Dowex 50 W and Amberlite IR-120) polymeric ion-exchange resins were carried out between 333-348 K. When these catalysts were used as commercially available, Amberlyst-15 was observed to be the most effective catalyst with respect to rate constants, but after drying it became the less effective one. The reaction rate increased with increase in catalyst concentration and reaction temperature. Stirrer speed and different mesh sizes had virtually no effect on the rate under the experimental conditions. The effect of divinylbenzene content was examined for the microporous resin Dowex 50W, and the results showed that the propionic acid conversion decreased as the divinylbenzene content was increased. The rate data were correlated with a second-order homogeneous reaction model. The apparent activation energies, reaction enthalpies and entropy values were calculated for each catalyst. Reaction monitoring is simple and fast by volumetric method and the reproducibility of this method was the order of ± %2.54.
[References]
  1. Chakrabarti A, Sharma MM, React. Polym., 20, 4, 1993
  2. Coutinho FMB, Souza RR, Gomes AS, Eur. Polym. J., 40, 1531, 2004
  3. Gerasimov Ya, Dreving V, Eremin E, Physical chemistry, Volume: 1, MIR Publishers, Moscow, 507, 1974
  4. Hart M, Fuller G, Brown DR, Dale JA, Plant S, J. Mol. Catal. A-Chem., 182, 445, 2002
  5. Hause JE, Principles of chemical kinetics, Wm.C. Brown Publishers, USA, 61, 1997
  6. Kirbaslar I, Baykal ZB, Dramur U, Turk J. Engin. Environ. Science, 25, 570, 2001
  7. Kirbaslar SI, Terzioglu H, Dramur U, Chin. J. Chem. Eng., 9, 93, 2001
  8. Levenspiel O, Chemical reaction engineering, John Wiley & Sons, Inc., Canada, 63, 1972
  9. Lilja J, Aumo J, Salmi T, Murzin DY, Maki-Arvela P, Sundell M, Ekman K, Peltonen R, Vainio H, Appl. Catal. A: Gen., 228, 255, 2002
  10. Lilja J, Murzin DY, Salmi T, Aumo J, Maki-Arvela P, Sundell M, J. Mol. Catal. A-Chem., 182, 556, 2002
  11. Liu WT, Tan CS, Ind. Eng. Chem. Res., 40(15), 3281, 2001
  12. Mahajani SM, React. Funct. Polym., 43, 254, 2000
  13. Park SW, Cho HB, Suh DS, Kim CW, Korean J. Chem. Eng., 16(2), 221, 1999
  14. Rodriguez O, Setinek K, J. Catal., 39, 449, 1975
  15. Roy R, Bhatia S, J. Chem. Technol. Biotechnol., 37, 6, 1987
  16. Weissermel K, Arpe HJ, Industrial organic chemistry, 2nd revised and extended edition, VCH Publishers Inc., New York, 289, 1993
  17. Xu ZP, Chuang KT, Can. J. Chem. Eng., 74, 494, 1996
  18. Yadav GD, Bhagat RD, J. Mol. Catal. A-Chem., 235, 101, 2005
  19. Yadav GD, Kulkarni HB, React. Funct. Polym., 44, 164, 2000
  20. Yadav GD, Mehta PH, Ind. Eng. Chem. Res., 33(9), 2198, 1994