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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 20 (1982), S. 641-650 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Carbon-13 nuclear magnetic resonance relaxation parameters have been obtained as a function of temperature for a set of branched polyethylenes whose β transition temperatures were determined independently. Resolvable spectra could be obtained at temperatures either corresponding to or very close to the temperature of the β transition. Together with results for other systems, these observations preclude the indentification of the β transition with the glass temperature. From the measured spin relaxation times and nuclear Overhauser enhancements average correlation times were calculated as a function of temperature. The average correlation times were calculated as a function of temperature. The average correlation time is on the order of 10-8-10-9 s at the β transition. These results argue strongly against it being assigned to the glass temperature.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 17 (1978), S. 1381-1384 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    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 19 (1981), S. 631-651 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The carbon-13 NMR linewidth (proton decoupled) of linear and branched polyethylenes crystallized so as to yield different supermolecular structures, as well as a polyethylene oxide sample, have been studied in detail. The purpose has been to assess the different molecular contributions to the linewidth in the completely amorphous polymer as well as in the amorphous regions of the semicrystalline state. These studies on a number of different structures were complemented by both proton-decoupled and dipolar-decoupled magic-angle spinning experiments on a particular sample, as well as frequency dependence studies. It is found that the abnormally broad resonance lines previously reported for the molten polymer can be significantly reduced by adopting appropriate methods of sample preparation and magnetic-field homogenization at each temperature. Relatively narrow lines result which can be interpreted in a conventional manner. In the semicrystalline state, the resonance lines are relatively broad and are shown to be morphology dependent. Specific contributions and their temperature dependence are discussed.
    Additional Material: 7 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 23 (1985), S. 367-385 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: High-resolution proton-decoupled carbon-13 nuclear magnetic resonance relaxation parameters have been obtained as a function of temperature for a set of completely amorphous polymers, semicrystalline polymers, and a series of ethylene-vinyl acetate copolymers. With these samples the nature of the glass temperature, other postulated amorphous transitions, and the β transition were investigated. For the completely amorphous polymers, the average correlation times depend on temperature according to the Williams-Landel-Ferry relation. Spectral collapse occurs at temperatures whose ratio to Tg is in the range 1.2-1.4 and corresponds to a correlation time of about 10-7s. The loss of resolvable spectra is demonstrated to be a consequence of experimental methods and is not due to the occurrence of another amorphous transition. Both the methylene and methine carbons can be resolved for the ethylenevinyl acetate copolymers. Although the correlation time for the methylene carbon is continuous and resolvable through the β transition region, the methine branch-point resonance is lost. The implication of these results to the molecular nature of the β transition is discussed.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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