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  • 1975-1979  (7)
  • 1970-1974
  • 1978  (7)
  • Chemistry  (7)
Material
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  • 1975-1979  (7)
  • 1970-1974
Year
Keywords
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 179 (1978), S. 269-271 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science: Macromolecular Reviews 13 (1978), S. 241-281 
    ISSN: 0076-2083
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 11 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 22 (1978), S. 1451-1457 
    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 thermal and photochemical oxidation of anthraquinone- and p-benzoquinone-doped polypropylene has been studied by absorption, luminescence, and infrared spectroscopy. Prior to irradiation, fluorescence and phosphorescence measurements showed that some of the anthraquinone and most of the p-benzoquinone had been converted into their corresponding hydroquinones during processing. The p-benzoquinone, unlike anthraquinone, also imparted a blue coloration to the polymer before irradiation, which is associated with the formation of a quinhydrone complex (or complexes). These results indicate that the quinones are thermally reduced to their corresponding hydroquinones during processing by a mechanism of hydrogen atom abstraction from the polymer substrate. On photo-oxidation, whereas anthraquinone acted as a photosensitizer, p-benzoquinone acted as a photostabilizer.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 3277-3282 
    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 photostabilization of commercial polypropylene by a hindered amine stabilizer is examined by luminescence and ESR spectroscopy. The presence of the amine stabilizer inhibits the photolysis of the α,β unsaturated carbonyl impurity groups present in the polymer. Examination by ESR, of the stabilized polymer before and after irradiation shows the development of a highly stabilized free radical indicating that the stabilizer can act as an ultraviolet stable antioxidant. Possible mechanisms whereby the hindered amine inhibits the photolysis of the α,β unsaturated carbonyl groups are discussed.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 611-614 
    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
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 625-631 
    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 fluorescence and phosphorescence excitation and emission spectra of commercial poly(4-methylpent-1-ene) are examined using a fully compensated spectrofluorometer. The excitation spectra of the polymer are compared with the absorption spectra of model chromophores of those believed to be present in the polymer. The fluorescence emission is primarily associated with the presence of enone and the phosphorescence with dienone impurity chromophoric units. Bromination of cold hexane extracts of the polymer significantly reduces the intensity of the fluorescence, confirming the presence of ethylenic unsaturation. The behavior of the luminescent enone and dienone groups during irradiation under sunlight-simulated conditions is also examined. Possible mechanisms for the participation of these chromophoric units in the photo-oxidation of poly(4-methylpent-1-ene) are discussed.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 22 (1978), S. 2085-2092 
    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 photodegradation of poly(ethylene 2,6-naphthalate) is examined by absorption and emission spectroscopy and by flash photolysis techniques. A comparison of the emission spectra with that of a model compound 2,6-dimethynaphthalate (DMN) shows that the chromophoric species responsible for light absorption in the near ultraviolet is the unit structure of the polymer itself. A flash photolysis study of DMN indicates that the major primary process in photodeterioration of the polymer involves scission by decarboxylation at the naphthyl-carbon bond.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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