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Membranes in Chiral.Separations

L. J. Brice, W. H. Pirkle, Enantioselective transport through liquid membranes in Chiral separations, applications and technology, S. Ahuja (Ed.), American Chemical Society, Washington... [Pg.22]

Membranes in chiral separations Kemmere, M. F. Keurentijes, J.T. F. Chiral Sep. Tech. (2nd Ed.) (2001), 127-150 Ed Subra-manian, G. Publisher Wiley-VCH Verlag GmbH, Weinheim, Germany. [Pg.76]

Membranes based on CD polymers are often used today in separation processes an increasing attention is paid now especially to chiral separation processes. In this aspect the use of chitosan/CD composite membranes in chiral separation of tryptophan was described. In the final part the selected examples of supramolecular architectures based on CD polymers are presented having in view the rapid development of supramolecular chemistry. [Pg.817]

In general, a liquid membrane for chiral separation contains an enantiospecific carrier which selectively forms a complex with one of the enantiomers of a racemic mixture at the feed side, and transports it across the membrane, where it is released into the receptor phase (Fig. 5-1). [Pg.128]

Since in most cases only one enantiomer possesses a desired pharmacological activity, it is necessary to construct enantioselective sensors to improve the quality of analysis due to the high uncertainty obtained in chiral separation by chromatographic techniques.315 For this purpose, enantioselective amperometric biosensors and potentiometric, enantioselective membrane electrodes have been proposed.264 The selection of one sensor from among the electrochemical sensor categories for clinical analysis depends on the complexity of the matrix because the complexity of different biological fluids is not the same. For example, for the determination of T3 and T4 thyroid hormones an amperometric biosensor and two immunosensors have been proposed. The immu-nosensors are more suitable (uncertainty has the minimum value) for direct determination of T3 and T4 thyroid hormones in thyroid than are amperometric biosensors. For the analysis of the same hormones in pharmaceutical products, the uncertainty values are comparable. [Pg.87]

Liquid-liquid extraction is a basic process already applied as a large-scale method. Usually, it does not require highly sophisticated devices, being very attractive for the preparative-scale separation of enantiomers. In this case, a chiral selector must be added to one of the liquid phases. This principle is common to some of the separation techniques described previously, such as CCC, CPC or supported-liquid membranes. In all of these, partition of the enantiomers of a mixture takes place thanks to their different affinity for the chiral additive in a given system of solvents. [Pg.15]

J. T. F. Keurentjes, F. J. M. Voermans, Membrane separations in the production of optically pure compounds in Chirality and Industry II. Developments in the Manufacture and applications of optically active compounds, A. N. Collins, G. N. Sheldrake, J. Crosby (Eds.), John Wiley Sons, New York (1997) Chapter 8. [Pg.22]

In this chapter we will provide an overview of the application of membrane separations for chiral resolutions. As we will focus on physical separations, the use of membranes in kinetic (bio)resolutions will not be discussed. This chapter is intended to provide an impression, though not exhaustive, of the status of the development of membrane processes for chiral separations. The different options will be discussed on the basis of their applicability on a large scale. [Pg.128]

In supported liquid membranes, a chiral liquid is immobilized in the pores of a membrane by capillary and interfacial tension forces. The immobilized film can keep apart two miscible liquids that do not wet the porous membrane. Vaidya et al. [10] reported the effects of membrane type (structure and wettability) on the stability of solvents in the pores of the membrane. Examples of chiral separation by a supported liquid membrane are extraction of chiral ammonium cations by a supported (micro-porous polypropylene film) membrane [11] and the enantiomeric separation of propranolol (2) and bupranolol (3) by a nitrate membrane with a A/ -hexadecyl-L-hydroxy proline carrier [12]. [Pg.130]

Possible applications of MIP membranes are in the field of sensor systems and separation technology. With respect to MIP membrane-based sensors, selective ligand binding to the membrane or selective permeation through the membrane can be used for the generation of a specific signal. Practical chiral separation by MIP membranes still faces reproducibility problems in the preparation methods, as well as mass transfer limitations inside the membrane. To overcome mass transfer limitations, MIP nanoparticles embedded in liquid membranes could be an alternative approach to develop chiral membrane separation by molecular imprinting [44]. [Pg.136]

Novel chiral. separations using enzymes and chiral surfactants as carriers have been realized using facilitated transport membranes. Japanese workers have reported the synthesis of a novel norbornadiene polymeric membrane with optically active pendent groups that show enantio.selectivity, which has shown promi.se in the. separation of propronalol. [Pg.430]


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