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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 50 (1961), S. 227-243 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The application of the sand columm extraction, fractional coacervation, and coacervate extraction methods to the molecular weight fractionation of polypropylene is described. Extremely reproducible results are given by the sand column method, and ten fractions taken by this method are adequate for characterization of the usual polypropylene distribution. The variation between the molecular weight distributions derived from six fractionations of a test polypropylene by the three methods was small and indicates that fraction polydispersity probably contributes negligibly to any deviation of the experimental distributions from the true distribution. Polypropylenes made with aluminum triethyl-transition metal trichloride catalysts contain relatively large amounts of low molecular weight polymer and have broad distributions similar to that of low-pressure polyethylene. All such polypropylene samples had distributions which were described well by a logarithmic normal equation with a constant standard deviation. The distribution was not altered when the aluminum triethyl in the catalysts was replaced by aluminum triisobutyl. Catalysts containing vanadium as the transition metal, however, produced polypropylenes with distributions distinctively different from those made with titanium trichloride.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 56 (1962), S. 485-499 
    ISSN: 0022-3832
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The molecular weight distributions of polypropylene samples subjected to various degrees of thermal degradation were experimentally determined and compared with those expected theoretically for random scission of the polymer chains. The comparison demonstrated that the chain breakage is predominately random and also indicates that current methods of determining molecular weight distributions are adequate for use in evaluating hypothesized degradation mechanisms. In terms of the free radical depolymerization theory, intermolecular transfer of the radical is the dominant process. A curve relating the degree of degradation to the intrinsic viscosity was obtained from calculations based upon a random degradation. With this curve, intrinsic viscosities measured as a function of degradation time could be used to obtain the time dependence of the degree of degradation. The observed degradation rates could not be described by a simple process in which the rate of bond rupture was proportional to the number of bonds present. Neither a similar process involving two bond types nor a dependence of the free radical diffusion rate upon the degree of degradation was by itself a satisfactory basis for interpreting the kinetics. The activation energy estimated for the polypropylene degradation at 250-300°C. was not significantly different from that determined by volatilization measurements at higher temperatures.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 2 (1964), S. 281-283 
    ISSN: 0449-2986
    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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