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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 18 (1980), S. 2313-2322 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The lateral thermal motion of atoms in an inextensible polymer chain would cause a shortening along the chain direction. This effect could explain the observed negative thermal expansivity α along the chain direction of a polymer crystal. Using this idea, the expansivity α is calculated for a lattice of parallel linear chains. A value of -1.3 × 10-5 K is obtained for chains with a carbon backbone, in good agreement with data for polyethylene.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 19 (1981), S. 335-352 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Measurements on the thermal expansivity α∥ and α⊥ (along and normal to the draw direction, respectively) have been carried out for a series of oriented polymers with widely different crystallinities (0.36-0.81) and draw ratios (1-20) and over large temperature ranges covering the major amorphous transitions in each case. While α⊥ increases with temperature, α∥ tends to decrease sharply above the transition temperature. For highly crystalline polymers, α∥ decreases to values typical of polymer crystals (-1 × 10-5 K-1) and this can be attributed to the constraining effect of the crystalline bridges connecting the crystalline blocks. However, for polymers of lower crystallinity, α∥ may become an order of magnitude more negative and this remarkable phenomenon is attributed to the rubber-elastic contraction of taut tie-moleucles. Since taut tie-molecules and bridges have drastically different effects on α∥ at high temperatures, this allows a rough determination of their relative fractions.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 22 (1984), S. 979-991 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: A linear chain model is used to calculate the thermal expansivities of polymer crystals from room temperature down to liquid-helium temperature. Because of restraint by strong covalent forces, vibrations along the chains give a negligible contribution. Vibrations transverse to the chains cause the length projected along the chain direction to decrease. The expansivity along the chain direction, αc∥ is therefore negative, and has temperature dependence characterized by the low Debye temperature of transverse vibrations. These vibrations, through a cubic term in the interchain van der Waals potential, also cause a positive expansivity, αc⊥ perpendicular to the chain direction. The theoretical predictions for αc∥ and αc⊥ agree quite well with experimental data over the wide temperature range under consideration.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 19 (1981), S. 971-981 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The thermal expansivity of polymer crystals in the direction parallel to the chain axis α∥ is studied in a planar zig-zag chain model. Using values of force constants for polyethylene, it was found that α∥ = -1.3 × 10-5 K-1, in good agreement with experimental results. Torsional modes are found to contribute slightly more than half α∥. The expansivity is independent of the mass of the atomic groups on the chain and only weakly dependent on the interchain van der Waals interaction.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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