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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 17 (1983), S. 143-148 
    ISSN: 1612-1112
    Keywords: Liquid chromatography ; Intermolecular interactions ; Adsorption from solutions ; Chemically modified layers in LC ; Conformation of bonded chains
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary For the investigation of intermolecular interactions in adsorption from solution, which are the basis of selectivity in molecular liquid chromatography (LC), it is convenient to use the LC method itself. Using this method the Henry's constants, K1, and other thermodynamic adsorption characteristics of hydrocarbons and of a series of polar substances on hydroxylated silica surface were determined from aqueous solutions. On the basis of the adsorption of hydrocarbons from water solutions the structure of the chemically modifying layers formed by different hydrocarbon groups on the silica surface is considered. The role of conformation ability of straight-chain bonded phases is demonstrated. Hydrocarbons are adsorbed on the hydroxylated silica surface more strongly from aqueous solutions than from solutions in saturated hydrocarbons and their retention increases with the increase in the number of carbon atoms in the molecule. The retention in LC is determined by the intermolecular interaction of the solute and solvent molecules with the adsorbent, as well by the contribution of the intermolecular interaction, between the solute and the solvent. The thermodynamic characteristics of adsorption of cymarin from water-ethanol solutions on hydroxylated silica gel and on silica gel surface modified by diphenylsilyl groups is compared. The solubility of silica gel modified by diphenylsilyl groups at different composition of water-ethanol eluent at different temperatures is investigated.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1612-1112
    Keywords: Chemical modification of silica ; Liquid chromatography ; Cardiac glycosides ; Chromatographic investigation of adsorption from solution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The chemical modification of silica surface using dichlorosilanes with methyl and phenyl groups and triethylamine as donor in the liquid phase was investigated. This modification leads to a dense coverage of the silica surface by the organic functional groups. Liquid chromatography permits the determination of the thermodinamic characteristics of intermolecular interactions of different molecules during adsorption from solutions on the modified surface of the silica. Silica gels modified with dichlorosilanes containing phenyl groups, possess high selectivity (α) and capacity (k′) for the cardiac glycosides G-strophanthin, K-strophanthoside, K-strophanthin-β and cymarin using water-alcohol mixture as the mobile phase, and the selectivity and capacity is much higher than observed on silica gels modified with methyl groups only.
    Type of Medium: Electronic Resource
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