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Ultrasound Assisted Heteropoly Acid Catalyst SiW12/SiO2 for Synthesis of Benzyl Acetate
Corresponding Author(s) : Xiao-Ping Lu
Asian Journal of Chemistry,
Vol. 25 No. 2 (2013): Vol 25 Issue 2
Abstract
Under ultrasonic radiation, benzyl acetate is synthesized from benzyl alcohol and glacial acetic acid in presence of catalyst SiW12/SiO2. The catalyst was prepared and characterized by IR, X-ray diffraction and SEM in the experiment. The XRD result indicates that heteropoly acid retains the Keggin-type structure. The kinetic parameters of reaction were, respectively measured at 90, 100 and 110 ºC and the kinetic equation was built. Then, the effects of reaction temperature, the amount of catalyst, molar ratio of benzyl alcohol to glacial acetic acid and ultrasonic intensity on the esterification yield were discussed. The results showed that the optimum operating parameters for the present work when 10 kHz ultrasonic frequency and 1.0 W/cm2 ultrasonic intensity are as follows: reaction temperature: 110 ºC, use amount of catalyst: 1.5 g, molar ratio of benzyl alcohol to glacial acetic acid: 1.5; reaction time: 75 min. Under such conditions, the esterification yield of the reaction reached above 95.3 %.
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- B.M. Abir, S. Bhupender, D. Debjit, S. Sushabhan and N.G. Munishwar, Bioorg. Med. Chem. Lett., 16, 4041 (2006).
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References
B.M. Abir, S. Bhupender, D. Debjit, S. Sushabhan and N.G. Munishwar, Bioorg. Med. Chem. Lett., 16, 4041 (2006).
Q.D. You, S. Feng, J.B. Jia and Q. Kun, J. Mol. Catal. A, 165, 33 (2001).
Z.G. Jian, H.C. Xiao, L. Dan, X.T. Zhang, Z.D. Hu and Z.L. Sun, Catal. Commun., 5, 473 (2004).
S. Takeshi, O. Ryuichiro, Z. Jin, M. Atsuyuki, C.K. Yui and O. Toshio, Catal. Today, 116, 179 (2006).
F.B. Fatemeh, M.H. Majid, R. Mina and A. Mina, J. Mol. Catal. A, 255, 193 (2006).
J. Pozniczek, A. Lubanska, A.D. Micek-Ilnicka, E.L. Mucha and A. Bielanski, Appl. Catal. A, 298, 217 (2006).
R. Palcheva, A. Spojakina, L. Dimitrov and K. Jiratova, Micropor. Mesopor. Mater., 122, 128 (2009).
G. Karthikeyan and A. Pandurangan, J. Mol. Catal. A, 311, 36 (2009).
Y.C. Wang, X.H. Yi and Wen Qin, Asian J. Chem., 24, 217 (2012).
X.-C. Yu, D.-L. Sun and X.-S. Li, Asian J. Chem., 24, 217 (2012).
J. Mason and E.D. Cordemas, Trans. Ichem. E, 74, 409 (1996).
G.D. Vishwanath, R.G. Parag and B.P. Aniruddha, Ultrason. Sonochem., 16, 345 (2009).
F.M. Zhang, Y.J. Zhong, W.D. Zhu and J. Wang, China Pet. Process. Petrochem. Technol., 36, 1144 (2007).
G.D. Vishwanath, R.G. Parag and B.P. Aniruddha, Chem. Eng. J., 145, 351 (2008).
M. Helen, B. Viswanathan and S.M. Srinivasa, J. Membr. Sci., 292, 98 (2007).
Y. Han, X. Chen, J. Wang, X.P. Lu and P.F. Han, Fine Chem., 27, 382 (2010) in Chinese.
B. Deng, A.H. Zhang and A.W. Xu, Fine Chem., 30, 53 (2009) (in Chinese.)