Issue
Korean Journal of Chemical Engineering,
Vol.34, No.6, 1661-1668, 2017
Esterification of acrylic acid with ethanol using pervaporation membrane reactor
Esterification of acrylic acid with ethanol was carried out using an in-situ reactor with an integrated pervaporation assembly (IPAE) made of polyvinyl alcohol (PVA) membrane and was compared with a non-integrated (NIE) system. Effect of reaction temperature (Tr), catalyst loading (Cc), molar ratios of reactants (MR) and ratio of effective membrane area to unit volume of reaction mixture (S/Vo) on kinetics of esterification reaction were studied. Conversions achieved in IPAE were found to be distinctly higher than the NIE. The highest conversion of acrylic acid was obtained as 83.3% at Tr=60 °C, MR=3 : 1, Cc=2% and S/Vo=14.1m-1. Equilibrium conversion of acrylic acid in NIE was obtained as 55.1% at 60 °C, 1 : 1 in 7 h, while using IPAE conversion enhances to 67.6%. Esterification of acrylic acid and ethanol with presently studied operating parameters provides a new approach to existing literature reported esterification-pervaporation system.
[References]
  1. Han Y, Lv EM, Ma LL, Lu J, Chen KX, Ding JC, Energy Conv. Manag., 106, 1379, 2015
  2. Truong HT, Rode S, Roizard D, Mouzon-Pelletier S, Tretjak S, Sep. Purif. Technol., 120, 24, 2013
  3. Zhu MH, Kumakiri I, Tanaka K, Kita H, Microporous Mesoporous Mater., 181, 47, 2013
  4. Park BG, Korean J. Chem. Eng., 21(4), 882, 2004
  5. Song KM, Hong YK, Yu J, Hong WH, Korean J. Chem. Eng., 19(2), 290, 2002
  6. Malshe VC, Chandalia SB, Chem. Eng. Sci., 32, 1530, 1977
  7. Sert E, Atalay FS, Chem. Eng. Process., 81, 41, 2014
  8. Sanz MT, Gmehling J, Chem. Eng. J., 123(1-2), 9, 2006
  9. Korkmaz S, Salt Y, Hasanoglu A, Ozkan S, Salt I, Dincer S, Appl. Catal. A: Gen., 366(1), 102, 2009
  10. Hasanoglu A, Salt Y, Keleser S, Dincer S, Desalination, 245(1-3), 662, 2009
  11. Delgado P, Sanz MT, Beltran S, Nunez LA, Chem. Eng. J., 165(2), 693, 2010
  12. Teerachaiyapat T, Ramakul P, Korean J. Chem. Eng., 33(1), 8, 2016
  13. Rathod AP, Wasewar KL, Sonawane SS, Procedia Eng., 51, 456, 2013
  14. Kita H, Horii K, Ohtoshi Y, Tanaka K, Okamoto KI, J. Mater. Sci. Lett., 14(3), 206, 1995
  15. Rathod AP, Wasewar KL, Sonawane SS, Procedia Eng., 51, 330, 2013
  16. Ma J, Zhang MH, Lu LY, Yin X, Chen J, Jiang ZY, Chem. Eng. J., 155(3), 800, 2009
  17. Zhu MH, Feng ZJ, Hua XM, Hu H, Xia SL, Hu N, Yang Z, Kumakiri I, Chen XS, Kita H, Microporous Mesoporous Mater., 233, 171, 2016
  18. Zhang W, Na S, Li W, Xing W, Ind. Eng. Chem. Res., 54, 18, 2015
  19. Altiokka MR, Citak A, Appl. Catal. A: Gen., 239(1-2), 141, 2003
  20. Wasewar K, Patidar S, Agarwal VK, Desalination, 243(1-3), 305, 2009
  21. Ameri E, Moheb A, Roodpeyma S, Chem. Eng. J., 162(1), 355, 2010
  22. Jyoti G, Keshav A, Anandkumar J, Int. J. Chem. React. Eng., 14, 571, 2016
  23. Ali SH, Tarakmah A, Merchant SQ, Al-Sahhaf T, Chem. Eng. Sci., 62(12), 3197, 2007
  24. Bart HJ, Reidetschlager J, Schatka K, Lehmann A, Ind. Eng. Chem. Res., 33(1), 21, 1994
  25. Yun ZOU, Zhangfa T, Kun LIU, Xianshe F, Chin. J. Catal., 31, 999, 2010
  26. Domingues L, Recasens F, Larrayoz MA, Chem. Eng. Sci., 54(10), 1461, 1999
  27. Liu QL, Zhang ZB, Chen HF, J. Membr. Sci., 182(1-2), 173, 2001
  28. Krupiczka R, Koszorz Z, Sep. Purif. Technol., 16(1), 55, 1999