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  Coupling of simulated moving bed technology and crystallization to separate enantiomers

Kaspereit, M., Lorenz, H., & Seidel-Morgenstern, A. (2002). Coupling of simulated moving bed technology and crystallization to separate enantiomers. In K. Kaneko (Ed.), Fundamentals of Adsorption 7 (pp. 101-108). Shinjuko, Japan: IK International Ltd.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0013-A114-F Version Permalink: http://hdl.handle.net/11858/00-001M-0000-0028-1B12-D
Genre: Conference Paper

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 Creators:
Kaspereit, M.1, Author              
Lorenz, H.1, Author              
Seidel-Morgenstern, A.1, 2, Author              
Affiliations:
1Physical and Chemical Foundations of Process Engineering, Max Planck Institute for Dynamics of Complex Technical Systems, Max Planck Society, ou_1738150              
2Otto-von-Guericke-Universität Magdeburg, External Organizations, ou_1738156              

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 Abstract: The separation of enantiomers is a diffcult task and important in the pharmaceutical industry. Often only with chromatographic methods the required high purity can be reached. In the last years the powerful simulated moving bed (SMB) process was applied successfully to separate a broad spectrum of racemic mixtures. However, chromatographic processes must still be considered as an expensive separation technology. Alternatively enantioseparation is often feasible by crystallization provided a certain enrichment has been achieved. In this work the combination of the two mentioned concepts is discussed.

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 Dates: 2002
 Publication Status: Published in print
 Pages: -
 Publishing info: -
 Table of Contents: -
 Rev. Method: -
 Identifiers: eDoc: 35050
 Degree: -

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Title: International Conference on Fundamentals of Adsorption - FOA 7
Place of Event: Nagasaki
Start-/End Date: 2001-05-20 - 2001-05-25

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Title: Fundamentals of Adsorption 7
Source Genre: Proceedings
 Creator(s):
Kaneko, K., Editor
Affiliations:
-
Publ. Info: Shinjuko, Japan : IK International Ltd.
Pages: - Volume / Issue: - Sequence Number: - Start / End Page: 101 - 108 Identifier: -