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  • 1970-1974  (4)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A-2: Polymer Physics 9 (1971), S. 499-515 
    ISSN: 0449-2978
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Studies were made on films of copolymers of ethylene with 0.5 and 1.0 mole-% carbon monoxide. The carbon monoxide appeared negligibly to affect the degree of crystallinity, melting point, morphology, and dynamic mechanical spectra. Infrared dichroism showed that the orientation of the carbonyl groups was comparable with that of the crystalline CH2 groups and indicated that the carbonyl groups are at least partially within the crystals. This is confirmed by x-ray measurements which indicate an expansion of the a-axis spacing and by an appreciable increase in the height of the α dielectric loss peak which has been assigned to crystalline motion. This α loss peak moves to a lower temperature with increasing carbonyl content, while the γ dielectric loss peak moves to higher temperatures. Activation energies of 25, 35, and 15 kcal/mole for the α, β, and γ peaks, respectively, were independent of carbonyl content and comparable with values for oxidized polyethylene.
    Additional Material: 15 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 11 (1973), S. 571-585 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An x-ray study has been made of the structure of a series of ethylene-phosphonic acid copolymers and the parent low-density polyethylene from which they were derived. The phosphonic acid contents (groups per 100 carbon atoms) of the copolymers were: A, 0.8; B, 1.8; C, 2.8; and D, 8.0. Small-angle x-ray scattering (SAXS) results show that the phosphonic acid substituents do not incorporate into the crystal lattice to any appreciable extent, that the substituents have the effect of decreasing the average thickness of the crystal lamellae and increasing the breadth of the size distribution of thicknesses, and that a two-phase model does not adequately account for the observed SAXS invariant. Wide-angle x-ray scattering (WAXS) results show that specimens, A, B, and C are partially crystalline with the polyethylene crystal structure and that D is amorphous. The observed broadenings of the 110 and 200 crystal reflections in the copolymers indicate that the substituents decrease the lateral dimensions of the crystalline lamellae and/or increase the deformation of the lattice due to external strain. Specimen D, completely amorphous according to the WAXS criterion, exhibits the largest value of the SAXS invariant of all the copolymers studied and must thus possess a multiphase structure consisting of small ordered regions and a disordered phase. The results of the study show the structure of the copolymers to be consistent with the fringe-micelle model but do not rule out the folded-chain model, although a regular fold surface is unlikely.
    Additional Material: 2 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 11 (1973), S. 1891-1939 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Dynamic x-ray diffraction and dynamic birefringence techniques are employed to determine the nature of the molecular motions associated with the α mechanical loss processes for low-density polyethylene. The results indicate that the low-temperature part of this loss (designated α1) is associated with an interlammellar “grain boundary” slip process while the higher temperature process (α2) involves intracrystalline motion and plasticity of the crystal itself. The activation energy for α1 determined by x-ray response is 25-30 kcal/mole, while that for α2 is 30-60 kcal/mole. The findings are consistent with dynamic infrared and dynamic light-scattering results which indicate that the motion of amorphous chains is closely correlated with that of the crystals. The relative contributions of amorphous and crystalline regions to the birefringence are dependent on the thermal treatment of the sample. The effect of static strain on the dynamic response indicates that crystal orientability is first increased with strain, probably because of splaying apart of lamellae, is subsequently decreased because of the restrictions of interlamellae tie chains, but then increases again as the spherulites are destroyed at high strain. The static strain reduces the orientability of amorphous regions.
    Additional Material: 29 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Letters Edition 11 (1973), S. 609-612 
    ISSN: 0360-6384
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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