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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 16 (1978), S. 2337-2342 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Hydrogen has been shown to be a true chain-transfer agent with some organometallic olefin polymerization catalysts. However, the Mayo equation for chain transfer in free-radical polymerization does not fit quantitative data from organometallic catalysts. There appear to be two reasons for the lack of fit. First, the Mayo equation considers the competition between hydrogen and olefin for the growing chain but does not account for their competitive absorption on the catalyst (coordination with vacant orbitals on the transition metal). Second, some organometallic catalysts gradually absorb hydrogen irreversibly to give a new catalyst species of altered behavior.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 2581-2597 
    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: Representative polyolefin films were exposed to UV radiation from light sources having different intensities and spectral distribution including the quartz mercury arc fluorescent lamps, xenon arc, and sunlight. Films exposed were polyethylene, polypropylene, and sensitized polyethylene. The oligomer fractions supported microbial growth, but the high polymers gave minimal or no growth. It was concluded that photooxidative degradation of polyolefins does not per se induce progressive attack by microorganisms. Oligomers present originally in the polymer are augmented by those produced by photooxidation. These oligomers support growth if separated from the polymer matrix. These observations explain some of the contradictory reports in the literature concerning the microbial degradation of sensitized polyolefins.
    Additional Material: 10 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 13 (1975), S. 1501-1509 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Recent work has shown that so-called chain-extended crystallization of polyethylene is crystallization of the newly discovered hexagonal phase. This hypothesis is supported by experiments on the pressure quenching of molten polyethylene.
    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 Part A: General Papers 1 (1963), S. 1041-1048 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The new applications of polypropylene glycols as chemical intermediates, particularly in the polyurethane field, have shifted emphasis from purely physical properties, such as density, viscosity, and volatility, to chemical properties, such as hydroxyl content, unsaturation, and molecular weight: Because much interest is also being shown in the uniformity of chain length, i.e., the “molecular purity” of the polypropylene glycol, methods were investigated for measuring this property. A liquid chromatographic procedure has been developed which will yield molecular weight distributions for polypropylene glycols in the 2025 number-average molecular weight range. The results approximate, but do not match, the values obtained by theoretical calculations. Details of the method and a typical distribution curve are presented.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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