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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 16 (1972), S. 539-543 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 4 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, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 18 (1974), S. 2501-2508 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Calorimetrically determined integral heats of solution and swelling ratio measurements carried out on extrudates of low-density polyethylene blended with Surlyn ionomer and ethylene-ethyl acrylate copolymer provide independent evidence for the redistribution of components as a result of extrusion. Although this evidence for “migration” supports earlier data for extrusion-triggered molecular redistribution in polyethylene, the present data further suggest that the effect may be due at least in part to the tendency of crystallizable polydisperse polymers to form cohesively weak boundary layers upon cooling from the melt. Thus, molecular redistribution effects may be expected in the processing of polyethylene and related thermoplastics but would not be pronounced in the extrusion of amorphous, narrow molecular weight distribution polymers, e.g., polystyrene.
    Additional Material: 3 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 Physics Edition 11 (1973), S. 15-24 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Thermodynamic interaction parameters have been calculated from gas-liquid chromatographic measurements for linear and branched polyethylene interacting with selected hydrocarbons. The values of the interaction parameter χ are substantial in spite of chemical similarities between the polymer and low molecular weight hydrocarbon species, a fact attributed to significant differences in the respective thermal expansion coefficients. A systematic increase of χ is observed in going from branched to linear polyethylene systems. The thermal expansion coefficients of these polymer homologs therefore may not be identical. The present χ values differ substantially from those reported in earlier literature. The comparison confirms suspicions that some older data, based on equilibrium sorption experiments, were erroneously low because of an underestimate in the reduced melting temperature of polymer in the presence of excess solvent.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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