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  • 1
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Ternary mobile phase compositions ; Solvation parameter model ; Mixture-design optimization
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A new approach is presented fro the prediction of retention in reversed-phase liquid chromatography using ternary mobile phase compositions. The solvation parameter model is used to create the system constants that characterize the properties of the mobile and stationary phases in terms of the relative ease of cavity formation, and differences in dispersion, lone pair electron, dipole-type, and hydrogen-bond association interactions for all solvent compasitions employed. A statistical mixture-design approach provides system surfaces and models for the variation of individual system constants as a function of ternary solvent composition. The models for the system surfaces allow the retention factor to be predicted as a function of mobile phase composition for any compound whose descriptor values are known, or can be obtained from estimation rules or determined by experiment. The method is validated using a large literature data base for the retention factor of up to 46 varied aromatic solutes in 72 methonolacetonitrile-water and methonol-tetrahydrofuran-water mobile phase compositions.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Solid-phase extraction ; Solvent effects ; Solvation parameter model ; Cyanopropylsiloxane-bonded, silica-based sorbent
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The solvation parameter model is used to characterize the retention properties of a cyanopropylsiloxane-bonded, silica-based sorbent with methanol, acetonitrile, tetrahydrofuran, and isopropanol in water as mobile phases. The system constants over the composition range 1 to 50% (v/v) organic solvent indicate that retention occurs because of the relative ease of cavity formation in the solvated stationary phase compared to the same process in the predominantly aqueous mobile phase as well as from more favorable stationary phase interactions with solutes containing π- and n-electrons. The capacity of the solute for dipole-type interactions is not important whereas all hydrogen-bond-type interactions result in reduced retention. Graphing the system constants as a function of mobile phase composition provides a simple mechanism for interpreting the change in capacity of the chromatographic system for retention in terms of changes in the relative weighting of fundamental intermolecular interactions. A comparison is also made with the retention properties of an octadecylsiloxane-bonded, silica-based sorbent with 30% (v/v) methanol in water as the mobile phase and the extraction characteristics of a porous polymer sorbent with 1% (v/v) methanol, acetonitrile, tetrahydrofuran, and isopropanol in water as the sample processing solvent. Changes in sorbent selectivity due to selective uptake of the processing solvent are much smaller for the cyanopropylsiloxane-bonded sorbent than the results found for a porous polymer sorbent.
    Type of Medium: Electronic Resource
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