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Adsorption chromatography Kowalska model

Abscisic acid (ABA), 784-785 Absorption measurement, 208 Acid dyes, 1015,1016 Adsorbent gradient, ISO Adsorbents, 17 Adsorption chromatography aluminas and, 17,107 Kowalska model of, 63-64 O ik model of, 61-62 Scott-Kucera model of, 62-63 silica gels and, 17,104 Synder-Soczewinski model of, 60 Alcoholic products, dyes from, 1005 Alkaloids from plants, 1040 pyrrolizidine, 1036-1040 Aluminas, 17,106-107 adsorption chromatography and, 107 partition chromatography and, 107 physical and chemical properties, 106-107 for separation of carbohydrates, 494 Amikacin, 458-461... [Pg.1091]

Kanamycin, 458-461 Kieselguhr, 107-108 for separation of carbohydrates, 494 Kowalska model of adsorption and partition chromatography, 63-64... [Pg.1096]

Further, the chiral discrimination model via the formation of ionic diastereomers, as proposed by Bhushan and Parshad [8] in Scheme 13.1, was viewed by Kowalska and coworkers [11] in terms of the energy difference for ion-pair formation (i.e., in the formation of the two diastereomeric salts). Ibuprofen is a carboxylic acid and, therefore, apt to dissociate (and form an organic anion) and the separation of the two enantiomers of ibuprofen can be achieved only because the thermodynamic equilibrium constants (K) for the ion-pair formation process for the two enantiomers (Ki and K2, respectively) have different numerical values. From the theory of adsorption liquid chromatography, it is well known [15] that the thermodynamic equilibrium constant of adsorption, K, can be defined as follows ... [Pg.341]


See other pages where Adsorption chromatography Kowalska model is mentioned: [Pg.63]    [Pg.64]    [Pg.63]    [Pg.64]   
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