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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Polymer International 41 (1996), S. 283-292 
    ISSN: 0959-8103
    Keywords: reaction injection moulding ; polyurea ; polyurethane-urea ; thermomechanical properties ; fracture behaviour ; 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: Segmented copolyureas (PUr) and copoly(urethane-urea)s (PUU) comprising 50% by weight of polyurea hard segments (HS) and polyether soft segment (SS) with different functionalities, have been formed by reaction injection moulding (RIM). The HS were formed from 4,4′-diphenylmethane diisocyanate reacted with mixed isomers of 3,5-diethyltoluene diamine. The nominal functionality of the SS prepolymers used (either amino- or hydroxyl-functionalised polyoxypropylenes with a constant molar mass per functional group of ∼ 2000 g mol-1) was systematically increased from 2 to 4. RIM materials were characterised using dynamic mechanical thermal analysis, differential scanning calorimetry, tensile stress-strain and fracture mechanics studies. Generally, the PUr exhibited far superior thermal-mechanical properties than equivalent PUU materials but inferior fracture resistance, owing to morphological variations resulting from differences in copolymerisation behaviour. For both systems, tensile behaviour was shown to be dominated by the degree of phase separation, whereas fracture properties showed a degree of dependence on SS functionality.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 697-707 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Furan-based diisocyanates and diamines were prepared unambiguously as potential monomers for polyurethane and polyamide production, starting from methyl furoate and furfurylamine, respectively. The syntheses were optimized and the product identity was confirmed by elemental analysis, IR and NMR spectroscopy, and also by preparation of derivatives which were similarly characterized.
    Additional Material: 1 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 709-723 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Novel furan-based diisocyanates (2a - c) were reacted with 1-butanol and basic kinetic studies were made. The results were compared with those obtained from 4,4′-methylenediphenylene diisocyanate (1) under similar conditions. The kinetics of these model reactions were found to be complex even in the presence of added catalysts. The isocyanates 2 studied, were shown to behave as benzylic type compounds with reactivities intermediate between those of aryl and alkyl diisocyanates. Comparative studies were made on segmented copolyurethanes prepared from 1 and from a furfuryl diisocyanate 2a having structural similarity to 1. The diol components used in these studies were 1,4-butanediol and polytetrahydrofuran. The segmented co-polyurethanes prepared from the furfuryl diisocyanate can thus be derived from a single naturally occurring source material, namely furfuraldehyde. These polymers were shown by differential scanning calorimetry and dynamic mechanical analysis to possess properties comparable to analogous copolyurethanes derived from oil-based sources.
    Additional Material: 8 Ill.
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