Please use this identifier to cite or link to this item: https://doi.org/10.1021/cg800546u
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dc.titleSelective crystallization of the metastable α-form of L-glutamic acid using concentration feedback control
dc.contributor.authorKee, N.C.S.
dc.contributor.authorTan, R.B.H.
dc.contributor.authorBraatz, R.D.
dc.date.accessioned2014-10-09T07:01:19Z
dc.date.available2014-10-09T07:01:19Z
dc.date.issued2009-07-01
dc.identifier.citationKee, N.C.S., Tan, R.B.H., Braatz, R.D. (2009-07-01). Selective crystallization of the metastable α-form of L-glutamic acid using concentration feedback control. Crystal Growth and Design 9 (7) : 3044-3051. ScholarBank@NUS Repository. https://doi.org/10.1021/cg800546u
dc.identifier.issn15287483
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/90094
dc.description.abstractA systematic methodology is presented for the selective crystallization of the metastable form of a monotropic dimorph, L-glutamic acid, for batch cooling crystallization. Attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectroscopy coupled with chemometrics was used to determine the solute concentration and solubility curves of both R- and -forms of L-glutamic acid in aqueous solution. The metastable limit associated with secondary nucleation for a seeded system was determined using laser backscattering (focused beam reflectance measurement, FBRM). Batch crystallizations seeded with the metastable R-form crystals following various preset supersaturation profiles were implemented using concentration feedback control which regulated the cooling rate based on the in situ measurement of solute concentration. Batch crystallizations operated at constant relative supersaturation in an appropriate temperature range prevented secondary nucleation of both polymorph types and were successful in selectively growing large metastable crystals with uniform size. © 2009 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/cg800546u
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1021/cg800546u
dc.description.sourcetitleCrystal Growth and Design
dc.description.volume9
dc.description.issue7
dc.description.page3044-3051
dc.identifier.isiut000267609600017
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