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  • 1
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    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 30 (1985), S. 4643-4651 
    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: During the development of an anionic butadiene telomerization process consisting of two stages, initiator preparation and telomerization, in a hydrocarbon solvent which contained a chain-transfer agent, we found that a small amount of oxygen accidentally introduced caused an unusually large decrease in the telomer viscosity. Based on the degree of such decrease due to the addition of oxygen at the two stages and based on the rather modest reactivity of oxygen with organosodium compounds, we concluded that free oxygen was catalytically involved in the telomerization process. The results of kinetic and transmetalation studies indicated that only the chain-transfer reaction was accelerated catalytically by free oxygen.
    Additional Material: 3 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 32 (1986), S. 3109-3116 
    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: Various liquid polybutadiene derivatives were examined as modifiers to improve the brittleness of phenolic resins. Amidated polybutadienes obtained from a maleinated polybutadiene and ammonia had the highest curing tendency when they were reacted with resole under mild conditions. The cured resins were homogeneous and the brittleness of the phenolic resins was remarkably improved. Crosslinking efficiency was closely related to the succinamic acid group of the amidated polybutadiene. Thermal behavior of the succinamic acid group was also related to the effects of curing temperature and curing time on crosslinking. From these observations, cross-condensation between the succinamic acid group of an amidated polybutadiene and resole seemed to have occurred to a great extent than the self-condensation of resole itself and oxidative crosslinking of the amidated polybutadiene.
    Additional Material: 6 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 32 (1986), S. 3675-3681 
    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: To prove the main cross-linking reaction between amidated polybutadiene and resole, cross-condensation reactions involving simple amide compounds and resole were examined. Amide compounds having both an amide group and a carboxylic acid group inhibited the self-condensation of resole itself. The cross-condensation products obtained from succinamic acid and 2-methylolphenol were separated using a preparative chromatography method to identify the cross-condensed products in which the main products were cross-condensed oligomers having an imide linkage. A cross-condensation scheme was proposed, and it was concluded that the main cross-linking reaction between amidated polybutadiene and resole also followed the same scheme.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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