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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 274 (1996), S. 634-639 
    ISSN: 1435-1536
    Keywords: Binary polymer mixtures ; dilute solutions ; semi dilute solutions ; overlap concentrationc *
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Using viscometry techniques on polymer fractions, we determine the critical concentrationc * (separating the dilute and semi dilute solutions). The same measurements have been conducted with mixtures of these fractions (mixtures 1:1 by weight of fractions differing in molecular mass and chemical nature, or fractions differing only in molecular mass). The determined values of critical concentrationc * of the mixtures are higher than the values calculated based on the critical concentrations of the corresponding fractions. This deviation from the additivity rule is attributed to the resistance in the interpenetration (delay to the attainment of the homogeneous state) between macromolecular coils of different chemical nature or of the same chemical nature but of different molecular mass. Higher values of the reduced viscosities of the mixture of the fractions, compared to the values calculated using the reduced viscosities of the corresponding fractions, are observed above the critical concentrationc *. In this concentration region the interaction parameter between two different polymers is calculated.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 27 (1989), S. 763-773 
    ISSN: 0887-6266
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A new gel permeation chromatography indirect calibration method is proposed for a polymer for which samples of known molecular weight and narrow molecular weight distribution are not available. This method is based on conversion of an experimentally obtained calibration curve for another polymer (polymer standard) through the universal calibration concept but using a new intrinsic viscosity-molecular weight relation. This indirect calibration curve is proposed especially for the low-molecular-weight region, where the method based on the Mark-Houwink-Sakurada equation gives erroneous results.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Using an equation derived from blob theory we calculate the number of statistical segments of which one blob consists (Nc). The same characteristic number can also be directly determined from the Mark-Houwink-Sakurada (MHS) representation. The above characteristic number depends only on the quality (i.e., properties) of the solvent and is found to be the same for different polymers if these polymers are dissolved in solvents for which the exponent in the MHS equation is the same. Based on the above determination of Nc, we calculate the adjustable parameter nα of thermal blob theory. The obtained value lies near a mean value of 10. Knowing the Θ temperature for a number of polymer-solvent systems, we propose a relation giving the Θ temperature as a function of the rigidity of the polymers and the properties of the solvents. Combining relations derived either from the two-parameter theory or from blob theory, we propose relations that give the adjustable parameter C relating the number of blobs of a chain to its excluded-volume parameter z. Knowing the adjustable parameter C (mean value 36) and using a relation derived also from the combination of the two-parameter theory with blob theory, we obtain the long range interaction parameter B of any polymer-solvent system. The obtained values are almost the same as the values obtained directly from the Stockmayer-Fixman-Burchard representation.
    Additional Material: 3 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 7 (1969), S. 335-341 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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