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  • 1980-1984
  • 1975-1979  (3)
  • 1977  (3)
  • Polymer and Materials Science  (3)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 15 (1977), S. 279-282 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Adiabatic compressibility measurements are reported on solutions in hydrocarbon solvents of a low Mw high ethylene content, and of both high and low Mw low ethylene content ethylene-propylene copolymers. In all solutions the observed adiabatic compressibility was lower than the solvent value by an increment which was a function of the solvent type. Comparison of the data for a high and low molecular weight sample of the same copolymer indicates no molecular weight effects. Changes in the composition of the copolymer, as indicated by NMR spectroscopy, have only a slight effect on the adiabatic compressibility. The dominant feature of these studies is the apparent correlation of the chain length of the alkane solvent with the decrement in the compressibility.
    Additional Material: 1 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: Polymer Physics Edition 15 (1977), S. 263-277 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Acoustic absorption and adiabatic compressibility measurements are reported on solutions of polystyrene (Mn = 89,000) in toluene and cyclohexane. The data in toluene cover a temperature range from 293 to 343°K and a concentration range of 10-400 Kg m-3 (1-40 wt%). The dependence of acoustic absorption on concentration was found to be linear up to 100 kg m-3, which corresponds to the concentration at which polymer-polymer interactions cause significant changes in the specific viscosity-concentration relationship. Up to 200 kg m-3 the data could be fitted to computations based on an artificial separation of the dispersion into contributions from viscoelastic and segmental processes, using parameters obtained from a study of narrow molecular weight distribution samples at 25 kg m-3. However, neither approach was capable of describing dispersions in the 300, 400 kg m-3 solutions. The modification of the relaxation spectrum observed at the highest concentrations is ascribed to volume and entropy changes associated with alterations of the local environment around a segment of the polymer chain. These changes have their origin in interchain penetration and polymer-polymer contacts, and indicate that ‘entanglement’ is primarily entropic in effect.The adiabatic compressibility exhibited similar deviations from a simple concentration dependence, and allowed estimation of an incompressible volume increment associated with polymer-polymer interactions in the high-concentration entangled matrix. However, the adiabatic compressibilities of solutions of polystyrene, 10-15 kg m-3, in cyclohexane showed no deviations from simple behavior in the region of the theta temperature. Measurements of the adiabatic compressibility of polystyrene in mixtures of cyclohexane-toluene have been used to obtain the relative magnitude of solvent and polymer contributions to the excess compressibility.
    Additional Material: 6 Ill.
    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: Polymer Chemistry Edition 15 (1977), S. 99-106 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The chemiluminescence emission from commercial samples of polytetrafluoroethylene, PTFE (Halon G-80 and Halon G-10), was studied at temperatures between 25 and 172°C. The emission intensity decreased on extended heating, removal of the surface layer, solvent extraction, or changing from an atmosphere of oxygen to an inert atmosphere. Films of PTFE deposited from the vapor phase showed comparatively little chemiluminescence under these conditions. Ozone-induced chemiluminescence was observed at 37°C from G-10 but not from G-80, or from films deposited from the vapor phase. The chemiluminescence intensity from ozone and G-10 was not reduced by solvent extraction.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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