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Received April 14, 2009
Accepted July 24, 2009
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Simulated moving-bed for separation of mandelic acid racemic mixtures
Department of Chemical Engineering, Chungnam National University, Daejeon 305-764, Korea 1Department of Chemical Engineering, Dong-A University, Busan 604-714, Korea 2School of Applied Chemistry, Kyung Hee University, Yongin 446-701, Korea
ihkim@cnu.ac.kr
Korean Journal of Chemical Engineering, January 2010, 27(1), 231-234(4), 10.1007/s11814-009-0339-8
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Abstract
Two enantiomers that constitute a racemate have different activities when employed as pharmaceuticals. Consequently, the pharmaceutical industry has been forced to market pure enantiomers instead of the racemic mixture. Simulated moving bed (SMB) is a chromatographic process that operates continuously without losing the enantiomeric purity of outlet streams from SMB. The present work describes the enantioseparation of mandelic acid in a labscale SMB unit. Chiral stationary phase was made by packing Kromasil TBB (O,O'-bis(4-tert-buylbenzoyl) -N,N'-diallyl-L-tartar diamid ) gel into empty columns. The outlet streams were sampled and analyzed by an analytical HPLC. Analysis indicated that purity values range from 82% to 94% according to the change of extract stream flow rate.
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References
McCoy M, Chemical and Engineering News, 78, 1 (2000)
Yoon TH, Lee E, Kim JM, Kim WS, Kim IH, Korean J. Chem. Eng., 25(2), 285 (2008)
Nicoud RM, Pharmaceutical Technology Europe, 11, 28 (1999)
Juza M, Mazzotti M, Morbidelli M, Trends in Biotechnology, 18, 108 (2000)
Park JS, Kim WS, Kim JM, Kim IH, J. Chem. Eng. Japan, 41 (2008)
Han SK, Yoo MS, Lee JK, Park TJ, Koo YM, Row KH, Korean Chem. Eng. Res., 41, 728 (2003)
Woo JH, Cho YS, Kim YD, Ahn DJ, Korean Chem. Eng. Res., 39, 685 (2001)
Kim BL, Kim JM, Kim WS, Kim IH, Korean Chem. Eng. Res., 46(4), 681 (2008)
Pedeferri M, Zenoni G, Mazzotti M, Morbidelli M, Chem. Eng. Sci., 54(17), 3735 (1999)
Mazzotti M, Storti G, Morbidelli M, Journal of Chromatography A, 769, 3 (1997)
Yoon TH, Lee E, Kim JM, Kim WS, Kim IH, Korean J. Chem. Eng., 25(2), 285 (2008)
Nicoud RM, Pharmaceutical Technology Europe, 11, 28 (1999)
Juza M, Mazzotti M, Morbidelli M, Trends in Biotechnology, 18, 108 (2000)
Park JS, Kim WS, Kim JM, Kim IH, J. Chem. Eng. Japan, 41 (2008)
Han SK, Yoo MS, Lee JK, Park TJ, Koo YM, Row KH, Korean Chem. Eng. Res., 41, 728 (2003)
Woo JH, Cho YS, Kim YD, Ahn DJ, Korean Chem. Eng. Res., 39, 685 (2001)
Kim BL, Kim JM, Kim WS, Kim IH, Korean Chem. Eng. Res., 46(4), 681 (2008)
Pedeferri M, Zenoni G, Mazzotti M, Morbidelli M, Chem. Eng. Sci., 54(17), 3735 (1999)
Mazzotti M, Storti G, Morbidelli M, Journal of Chromatography A, 769, 3 (1997)