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  • 1965-1969  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 4 (1966), S. 765-775 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The behavior of films of polyelectrolytes at the water-organic liquid interface depends on the nature of the interface and the pH of the substratum. The present paper investigates the influence of these two factors on the cohesive forces between monomer units. Two polyelectrolytes were studied: poly(methacrylic acid) (APM) and poly-2-vinylpyridine (2-PVP). In the case of uncharged films, the collapse pressure decreases when the polarity of the organic phase becomes more important, whereas the term ω/kT, which appears in the theory of Motomura and Matuura, increases. A quantitative relation between the parameter ω/kT and the collapse pressure may be deduced. The behavior of the ionized surface film at different pH values is modified by the choice of the interface. However, there exists a competition between two phenomena: the dissolution of ionized residues in the substratum and the electrostatic repulsion between charges in the surface plane. Depending upon whether the first or the second parameter is more important, we observed that the surface pressure decreased or increased with the degree of ionization.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 4047-4064 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Monolayers of poly-2-vinylpyridine (2-PVP), of poly(methacrylic acid) (PMA), as well as of a polyampholyte containing definite proportions of 2-vinylpyridine and acrylic acid were investigated at the air-water interface. We studied particularly the ionization of the film. The variation of surface pressure with respect to the nature of the ionic subsolution was analyzed. At constant degree of ionization, two factors determine the surface pressure: the valence and the dimension of the counterion. The polyampholyte may be considered alternatively as a polycation or a polyanion depending on the pH value of the support. The small concentration of dipolar ions permits the presence in the same macromolecule of the properties of the poly-2-vinylpyridine and of the poly(methacrylic acid). Qualitatively, the influence of the counterions is reproduced for the three polyelectrolytes. With monovalent ions, a quantitative approach is possible. The surface pressure is analyzed in terms of current theories of the ionic double layer. The application of the Gouy-Chapman model gives satisfactory results at different polymer and ionic concentrations. The theory has been extended with success to completely and incompletely ionized monolayers. However, there is evidence that the Gouy-Chapman theory is obeyed only at high areas. For denser films, the discrepancy between the calculated and experimental pressure is often quite large. The inclusion of a “fluctuation potential” contribution to the surface pressure permits a good agreement between the theory and the experiments.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 1965-08-01
    Print ISSN: 0950-7671
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Published by Institute of Physics
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