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  • Articles: DFG German National Licenses  (3)
  • 1985-1989  (3)
  • 1985  (3)
Source
  • Articles: DFG German National Licenses  (3)
Material
Years
  • 1985-1989  (3)
Year
  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 107 (1985), S. 1496-1500 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 189-203 
    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: It is shown that nitroso-tert-alkanes are highly active UV stabilizers which become at least partially chemically attached to polypropylene during processing. The aromatic nitroso compounds are less effective as light stabilizers but are more effective than their alkyl analogues as thermal oxidative stabilizers. Mechanisms are proposed to account for the antioxidant activity of the nitroso compounds and their ability to cause crosslinking of the polymer during processing.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 789-797 
    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 antioxidant mechanism of zinc dialkyl dithiocarbamate is examined in detail in model compounds. The kinetics of the reaction of zinc dialkyl dithiocarbamate with hydroperoxides were studied in inert and oxidizable substrates. A typical electron donor antioxidant and a base (CaCO3) were found to inhibit the peroxide decomposition. The oxidation products of the Zinc II complex appear to be quite different from those of the nickel II and iron III complexes. Two processes are involved in the antioxidant function of the zinc complex: The first is a free radical decomposition of the peroxides, which predominates at molar cumene hydroperoxide (CHP)/zinc diethyl dithiocarbamate (ZnDEC) ratios of 10 or less. At higher molar ratios an ionic reaction predominates, although there is a radical contribution at all ratios. Thiocarbamoyl disulfide does not seem to be formed as an intermediate from ZnDEC during the ionic process.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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