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  • Polymer and Materials Science  (2)
  • 1985-1989
  • 1965-1969  (2)
  • 1
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 1583-1595 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The paper describes the titration relations for nylon 66 samples of different endgroup contents both for aqueous and alcohol solutions. The effect of temperature change is also considered. The results are consistent with a zwitterion structure of the nylon, carboxyl groups being protonated on acid titration. The acid groups are shown to be weaker than the corresponding monomeric acids in aqueous solution, owing to their environment inside the polymer. Individual ionic affinities are calculated from the experimental absorption isotherms and are in agreement with values obtained from a simple electrostatic theory. The low sulfate ion affinity can be explained by assuming interaction for this ion with single, fixed, isolated sites.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-1: Polymer Chemistry 6 (1968), S. 1913-1923 
    ISSN: 0449-296X
    Schlagwort(e): Physics ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The paper deals with the diffusion of two mineral acids, hydrobromic and sulfuric acids, and two simple dye acids, NOG (C. I. Acid Orange 7) and SY (C.I. Food Yellow 3), in water-swollen nylon 66. Anion self-diffusion coefficients were obtained by radiotracer techniques. The bromide ion and the SY anion self-diffusion coefficients show very little variation with concentration in the amino-dyeing region, whereas the H2SO4 and NOG anion diffusion coefficients are concentration-dependent. The variation of the H2SO4 anion diffusion coefficient with concentration is consistent with the formation of small quantities of the highly mobile bisulfate ion. The low SO4 diffusion coefficient may be explained by the interaction of this ion with single, fixed sites in the polymer. The variation of the NOG anion diffusion coefficient with concentration does not follow a simple D = D0[1/(1 - θ)] relationship at intermediate concentrations but the rapid increase observed as the available sites became saturated, i.e., as θ → 1, is consistent with a site saturation model.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
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