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  • 1
    ISSN: 1572-8927
    Keywords: Aqueous solubility ; octanol-water partition coefficient ; activity coefficient ; n-propylbenzene ; ethylbenzene ; n-hexane ; di-isopropyl ether ; chloroform ; nitrobenzene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract From thermodynamics and certain assumptions it is shown that, under the usual experimental conditions, the octanol-water partition coefficient (Ko/w) of a given organic liquid should be the same whether the substance is partitioned neat or as part of a mixture. Measurements of several mixtures of n-propylbenzene (log Ko/w=3.71±0.04)+ethylbenzene (log Ko/w=3.16±0.01) clearly confirm this. It is also shown that the aqueous solubility (Sw) of a neat organic liquid can be related to its aqueous solubility (S w ′ ), when it is present at volume fraction ϕ in an organic liquid mixture, by S w ′ =γϕSw, where γ is its activity coefficient in the organic mixture. The measured S w ′ values for n-propylbenzene + ethylbenzene (γ≈1), n-hexane + nitrobenzene (γ〉1) and di-isopropyl ether + chloroform (γ〈1) are found to be in good agreement with the predicted values (average differences of, respectively, 〈2%, ≈8% and ≈6%). In general, the bounds on S w ′ are expected to be 0〈S w ′ 〈Sw.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Chromatographia 29 (1990), S. 313-321 
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Polystyrene homopolymers ; Isocratic and gradient elution ; Retention prediction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Isocratic and gradient elution high performance liquid chromatographic measurements of the retention behavior of polystyrene homopolymers with molecular weights ranging from 2 kD to 390 kD were performed using mixed methylene chloride-methanol mobile phases of varying composition and a C-18 chemically bonded stationary phase supported on either 100 Å or 300 Å mean pore diameter silica. Isocratic measurements of the capacity factor, k′, for different molecular weight homopolymers as a function of the volume fraction of methylene chloride, ϕ, permit determination of the critical composition, ϕc, which renders k′=1 and the local slope, S=−∂lnk′/∂ϕc of the lnk′-ϕ isotherm at ϕ=ϕc, and also the dependence of ϕc and S on the degree of polymerization, M. Linear gradient elution measurements of ϕc and S were also performed and compared to the corresponding isocratic measurements. The general retention behavior and the dependence of ϕc and S on M compare favorably to the predictions of the theory of homopolymer retention and fractionation developed by Boehm, Martire, Armstrong, and Bui (BMAB). Comparison is also made between the present work and the experimental observations of other workers on related chromatographic systems involving hompolymer retention.
    Type of Medium: Electronic Resource
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