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  • Chemistry  (4)
  • 1965-1969  (4)
  • 1965  (4)
Collection
Publisher
Years
  • 1965-1969  (4)
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 9 (1965), S. 3091-3099 
    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: Blends of cis-1,4-polybutadiene and natural rubber were vulcanized with dicumyl peroxide and a CBS (N-cyclohexylbenzothiazole-2-sulfenamide) accelerated sulfur system. For the peroxide-cured systems, soft vulcanizates had the natural rubber component only very lightly crosslinked and showed pronounced flow at room temperature. The oxidative stress relaxation of the hard vulcanizates at 80°C. in air was intermediate between that of the pure polymers. Intermittent stress relaxation measurements on these vulcanizates showed pronounced crosslinking during the aging of the pure polybutadiene and the 50/50 blend. Soft blends prepared by the accelerated sulfur system also showed flow due to the lightly crosslinked polybutadiene component. The unextracted hard blends resembled the pure polybutadiene vulcanizate in oxidative stress relaxation behavior at 80°C. in air, whereas after extraction to remove residual antioxidant and vulcanization products, etc., the blends were similar to natural rubber at all levels.
    Additional Material: 6 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 9 (1965), S. 3101-3109 
    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 effect of high strain on the oxidative stress relaxation of several natural rubber vulcanizates has been investigated. In the case of peroxide and CBS accelerated vulcanizates, the rate of stress relaxation increases with increasing strain, and this increase appears to be due to an increase in the rate of oxidation of the network. TMTD and MBT vulcanizates showed marked premature failure at high strains and no oxidative stress relaxation measurement could be made. It was found that the tensile strength of a TMTD vulcanizate was at least 20% higher in vacuum than in oxygen, due, it is believed, to stress-induced oxidative degradation at the tip of surface flaws in the rubber.
    Additional Material: 2 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 3 (1965), S. 977-984 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 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 3 (1965), S. 19-30 
    ISSN: 0449-2951
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polyamides of both cis- and trans-1,4-cyclohexanebis(methylamine) with aliphatic dicarboxylic acids and copolyamides of trans-1,4-cyclohexanebis(methylamine) with p-xylene-α,α′-diamine were prepared in order to discover the effect of cycloalkane rings on melting point. Analogous polyamides of p-xylene-α,α′-diamine were prepared for comparison. The polyamides of trans-1,4-cyclohexanebis(methylamine) had higher melting points than the analogous polyamides of p-xylene-α,α′-diamine. This result is believed to be due to the slightly contracted conformation which trans-1,4-cyclohexanebis(methylamine) can adopt in the polymer chain. The polyamides of cis-1,4-cyclohexanebis(methylamine) melted lower than those of the trans isomer. The lower symmetry of the cis-diamine accounts for this result. The melting points of the copolyamides of trans-1,4-cyclohexanebis(methylamine) and p-xylene-α,α′-diamine were higher than expected. It is suggested that these compositions are examples of partially isomorphous copolyamides.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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