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  • 1965-1969  (3)
  • 1935-1939
  • 1965  (3)
  • Polymer and Materials Science  (3)
Material
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  • 1965-1969  (3)
  • 1935-1939
Year
Keywords
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 2843-2851 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An analytic solution to Skeist's copolymerization equation has been obtained for the case of binary copolymerization. From this solution, a differential copolymer composition equation is also derived. For given values of the reactivity ratios, these equations then permit the convenient calculation of expected binary copolymerization behavior as a function of conversion. Critical conditions leading to incompatible copolymerizations are also discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 4000-4000 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 3 (1965), S. 1785-1792 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The storage and loss shear compliances (J′, J″) of poly(n-butyl methacrylate) (number-average molecular weight 320,000) were measured at frequencies between 0.08 and 1.0 cycle/sec. in the temperature range of 18-33°C., encompassing the glass transition. Data were obtained both at voluminal equilibrium and as a function of time during the slow isothermal contraction which follows a quench to a temperature near the transition. The latter data were supplemented by dilatometric measurements on similar samples to determine the magnitude of the volume contraction. Correlation of the dependences of J′ and J″ on temperature and on elapsed time (at constant frequency) indicated that the relaxation mechanisms are controlled primarily by free volume. The method of reduced variables was successfully applied to the dependence of J′ on temperature and elapsed time using shift factors aT,t calculated from the modified Doolittle equation and the magnitudes of volume contraction measured dilatometrically. The dependence of J″ on both temperature and elapsed time was more complicated, indicating a change in the shape of the retardation spectrum with free volume. The behavior is qualitatively very similar to that of poly(vinyl acetate), previously studied, except that the magnitudes of J′ are considerably larger and the thermal expansion coefficient of the free volume is smaller.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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