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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 6 (1995), S. 373-382 
    ISSN: 1042-7147
    Keywords: aromatic polyamides ; fractal polymers ; porous structure ; synthesis of rigid polymers ; dendrimers ; photon correlation spectrometry ; viscosity ; WAXD ; 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
    Notes: The preparation of rigid aromatic, highly branched polyamides is described. Owing to the method of preparation and the chosen ratio of difunctional to trifunctional monomers, these entities are highly porous and not dendrimeric in nature. They better conform with the fractal model and are therefore called fractal polyamides (FPs). The effects of variations in the polymerization procedure, in total monomer concentration, in the ratio of amine to carboxyl groups and in the duration of the polycondensation reaction are investigated. Some characterization was performed and the results are presented and briefly discussed.
    Additional Material: 2 Ill.
    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 : Wiley-Blackwell
    Polymers for Advanced Technologies 6 (1995), S. 383-393 
    ISSN: 1042-7147
    Keywords: interpenetrating blends ; nylon-6 ; rigid polyamides ; fractal polyamides ; 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
    Notes: Blends of nylon-6 and up to 20% rigid aromatic fractal polyamides (FPs) were prepared by precipitation from a mutual solvent and by two melt-processing procedures. In general, no grafting of the flexible linear nylon chains onto the rigid FPs took place, but in several instances of melt-blending of nylon with FPs whose amine end-groups were exposed, a low level of grafting occurred.The glass transition temperature and the tensile modulus and yield strength of the blends were greatly elevated as function of the FP concentration in the blends. This was demonstrated to be caused by the openness and rigidity of the FPs, and the connectivity of the FP segments through rigid branchpoints. The great porosity of the FPs allows the chains of the amorphous fraction of the nylon to interpenetrate and pass through the FPs, and the stiff segments of the FPs to suppress the chain motions of the nylon, which accounts for the enhanced glass transition temperature (Tg) and tensile properties. When non-porous amorphous silica particles or stiff linear or essentially unbranched zigzag polyamides were blended with the nylon, the Tg of the nylon either did not change at all or changed only very little. Several analytical procedures were used to verify that the nylon chains occupied most of the free space in the pervaded volumes of the FPs in the as-prepared blends and filled this space completely when these blends were compression-molded. The point where the FPs filled all the volume of the amorphous fraction of the nylon-6 was reached between 5 and 7.5% FP concentration. Below this, traces of the original nylon-6 Tg could be occasionally detected. Above it, only the high Tg of the nylon chains interpenetrated in the FPs was detected.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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