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  • 1
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 5 (1965), S. 246-253 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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: Studies of polypropylene oxyluminescence show the luminous intensity to be dependent upon the degre of oxidation. The length of the low intensity level portion of the luninescence curve, or pseudo induction period, was found to be a measure of the useful stabilizer life, and the intensity of this portion indicative of the effectiveness of stabilization. The effect of peroxide decomposers was studied and results indicate that peroxide reactions are major producers of luminescence. Analysis of the accepted modes of polymer oxidation, in view of our luminescence findings, indicate that the rate of luminescence buildup should depend upon ease of R. formation and the luminous intensity should be dependent on peroxy radical concentration. The effect of tertiary-carbon content on luminescence was also investigated, and luminous intensity was found to be dependent upon the amount of polymer branching. Model Compounds having slight structural variations were examined and were found to produce different intensity-time curves during oxidation, which may be attributed to ease of formation of a reactive site and subsequent peroxy radical reactions.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 2
    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: The faint emission of light by various classes and types of polymers when heated in the presence of oxygen, oxyluminescence, was studied by means of a photomultiplier tube and sensitive microammeter. Among the polymers with a carbon-carbon backbone, the polymers having the greater number of tertiary carbon atoms generally showed greater intensities of luminosity. Polystyrene was a notable exception to this generalization. The shape of the luminosity versus time curves varied with the type of polymer. It was also found that the emission of light did not stop instantly when the oxygen atmosphere was replaced by an inert gas, but rather followed an exponential type of decay. The rate of decay appeared to be different with different types of polymers. The intensities of luminescence and the times required to reach maximum or steady state luminescence were compared with oxygen uptake data for various polymers. In general there was a qualitative, but not necessarily quantitative correlation between the luminous intensities and polymer stabilities in the presence of oxygen.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 8 (1964), S. 997-1006 
    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: The oxyluminescence of polypropylene and polyethylene stabilized with various amounts of 4,4′-thiobis(3-methyl-6-tert-butylphenol) were studied and compared with oxygen uptake data. It was found that there was a correlation, although not linear, between the two methods. In the case of the stabilized polypropylenes, a pronounced aging effect was noticed. The oxyluminescent behavior of stabilized polyethylene was somewhat different from that of stabilized polypropylene. The temperature coefficients of the oxyluminescence of polypropylene, polyethylene, nylon 6, polystyrene, polyurethane and polymethyl methacrylate were obtained. From these data the apparent activation energies for the light-emitting reaction were calculated. For the olefin polymers, these values are close to the activation energies of the oxidative degradation reaction obtained by other means. Both polyethylene and polymethyl methacrylate have different activation energies below their transition points as compared to higher temperature, indicating a different mode of reaction in the solid state from that occurring in the melt. An interesting transition luminescence, which was more pronounced in the absence of oxygen, was observed in the case of polyethylene.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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