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  • 1985-1989  (3)
  • Polymer and Materials Science  (3)
  • Development
  • arachidonic acid
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 30 (1985), S. 1875-1891 
    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: Our limited success in toughening methylene dianiline (MDA)-cured Epon 828, using varying rubber types, led to a study of the role of the matrix viscoelasticity in the toughening process. Two rubber types, with different interfacial bonding capabilities, poly(n-butyl acrylate)/15 wt % acrylonitrile/2 wt % acrylic acid and poly(n-butylacrylate)/15 wt % acrylonitrile, were incorporated into systems containing varying amine concentrations to control crosslink density. Impact strengths of controls and rubber-modified compositions increased with excess amine concentrations up to 70%. The impact strengths for the poly(n-butyl acrylate)/15 wt % acrylonitrile/2 wt % acrylic acid rubber-modified compositions were greater than their equivalent controls, with the effect being greater at a lower crosslink density. This study confirmed that the matrix viscoelasticity is the controlling parameter in the toughening process. The degree of rubber-epoxy interfacial bonding is also an important parameter to consider, if the matrix viscoelasticity permits toughening. A modified stress response model was used to explain the toughening phenomenon.
    Additional Material: 19 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 26 (1988), S. 247-254 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Diepoxides and in-chain carbonate groups react readily in the presence of quarternary ammonium salts, although reaction is not observed without this catalyst. Two moles of epoxide react with each mole of carbonate. When diepoxides and polycarbonates are reacted, a three-dimensional network of chains crosslinked with carbonate groups is produced; the crosslink density is controlled by adjusting the epoxy/carbonate ratio. Tertiary amines and alkoxides also catalyze the epoxy/carbonate reaction, but these have the undesirable attribute of promoting epoxy polymerization. The presence of oligocarbonates accelerates the epoxy-amine reaction.
    Additional Material: 5 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 34 (1987), S. 2105-2124 
    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: Electro-copolymerization of methyl acrylate, acrylic acid, methacrylic acid, acrylamide, and methyl methacrylate with acrylonitrile onto graphite fibers has been successfully done in our laboratory. The coatings are relatively uniform and their properties, especially their modulus, can be systematically varied by controlling the monomer ratio in the eletrolyte solution. This technique is being used to introduce a ductile interlayer of contrlled composition and thickness between the composite fibers and matrix. Copolymers of methyl acrylate and acrylonitrile formed by this technique are random copolymers, with Tg′s varying from 10 to 90°C. These copolymers have fairly high molecular weight, in the range of 100,000 g/mol. Monomer reactivity ratios were determined, based upon free radical polymerization kinetics, from cyclic voltammetry. An indirect initiation mechanism is suggested. Bonding between interlayer and matrix can be improved by introducing vinyl monomers with proper functional groups, capable of reacting with the epoxy resin, at the last stage of the electropolymerization process.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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