Copyright (c) 2013 AJC
This work is licensed under a Creative Commons Attribution 4.0 International License.
Facile Biodiesel Synthesis from Esterification of Free Fatty Acids Catalyzed by SO3H-Functionalized Ionic Liquid
Corresponding Author(s) : Bo Wang
Asian Journal of Chemistry,
Vol. 25 No. 1 (2013): Vol 25 Issue 1
Abstract
The esterifications of free fatty acids with methanol were efficiently accomplished over a SO3H-functionalized ionic liquid, 1-(4-sulphonic acid)butyl-3-methylimidazolium hydrogen sulphate ([BSMim]HSO4), which are commonly considered as both one of the typical synthetic routes and the representative pretreatment process for biodiesel production. Particularly, the maximum yield of methyl oleate was obtained in 99.9 %. Methyl oleate could be isolated through simple decantation from the biphasic system, which is attributed to the immiscibility of [BSMim]HSO4 with hydrophobic ester and the good stability and operability of ionic liquid were demonstrated by the six times reuses without dramatic decrease in methyl oleate yield.
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- H.J. Berchmans and S. Hirata, Bioresour. Technol., 99, 1716 (2008).
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References
H.J. Berchmans and S. Hirata, Bioresour. Technol., 99, 1716 (2008).
S.P. Singh and D. Singh, Renew. Sustan. Energ. Rev., 14, 200 (2009).
P. Schinas, G. Karavalakis, C. Davaris, G. Anastopoulos, D. Karonis, F. Zannikos and S. Stournas, Biomass Bioenerg., 33, 44 (2009).
J.M. Marchetti, V.U. Mguel and A.F. Errazu, Renew. Sustan. Energ. Rev., 11, 1300 (2007).
J.M. Dias, M.C.M. Alvim-Ferraz and M.F. Almeida, Bioresour. Technol., 100, 6355 (2009).
P.D. Patil and S. Deng, Fuel, 88, 1302 (2009).
Y. Rezgui and M. Guemini, Ind. Eng. Chem. Res., 12, 4056 (2008).
G. Antolín, F.V. Tinaut, Y. Briceño, V. Castaño, C. Pérez and A.I. Ramírez, Bioresour. Technol., 83, 111 (2002).
M.D. Serio, M. Cozzolino, R. Tesser, P. Patrono, F. Pinzari, B. Bonelli and E. Santacesaria, Appl. Catal. A: Gen., 320, 1 (2007).
M.M. Teresa,A.A. Martins and N.S. Caetano, Renew. Sust. Energ. Rev., 14, 217 (2010).
M.A. Dubé, A.Y. Tremblay and J. Liu, Bioresour. Technol., 98, 639 (2007).
Z.S. Qureshi, K.M. Deshmukh, M.D. Bhor and B.M. Bhanage, Catal. Commun., 6, 833 (2009).
H. Zhao, Z.Y. Song, O. Olubajo and J.V. Cowins, Appl. Biochem. Biotechnol., 162, 13 (2010).
B.A. DaSilveira Neto, M.B. Alves,A.A.M. Lapis, F.M. Nachtigall, M.N. Eberlin, J. Dupont and P.A.Z. Suarez, J. Catal., 249, 154 (2007).
X.Z. Liang, G.Z. Gong, H.H. Wu and J.G. Yang, Fuel, 88, 613 (2009).
D. Fang, J. Cheng, Z. Fei, K. Gong and Z. Liu, Catal. Commun., 9, 1924 (2008).
J. Akbari and A. Heydari, Tetrahedron Lett., 29, 4236 (2009).
M.H. Han, W.L. Yi, Q. Wu, Y. Liu, Y.C. Hong and D.Z. Wang, Bioresour. Technol., 100, 2308 (2009).
X.Z. Liang and J.G. Yang, Green Chem., 12, 201 (2010).
J.H. Shen, H. Wang, H.C. Liu, Y. Sun and Z.M. Liu, J. Mol. Catal. A: Chem., 280, 24 (2008).
A.C. Cole, J.L. Jensen, L. Ntai, K.L.T. Tran, K.J. Weaver, D.C. Forbes and J.H. Davis, J. Am. Chem. Soc., 124, 5962 (2002).
H. Xing, T. Wang, Z. Zhou and Y. Dai, Ind. Eng. Chem. Res., 11, 4147 (2005).
D.Y.C. Leung, X. Wu and M.K.H. Leung, Appl. Energ., 87, 1083 (2010).
B.C. Ranu and S. Banerjee, Org. Lett., 14, 3049 (2005).
L. Zhang, M. Xian, Y.C. He, L.Z. Li, J.M. Yang, S.T. Yu and X. Xu, Bioresour. Technol., 100, 4368 (2009).
M.P. Dorado, E. Ballesteros, J.M. Arnal, J. Gòmez and F.J.L. Gimènez, Energ. Fuel, 17, 1560 (2003).