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  • Chemistry  (2)
  • polyurethane  (1)
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  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 35 (1997), S. 2991-2998 
    ISSN: 0887-624X
    Keywords: NMR spectroscopy ; polyurethane ; isophorone diisocyanate ; IPDI ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Chemical structure investigations of polyurethane binders based on difunctional linear glycidyl azide polymer (GAP) cured with isophorone diisocyanate (IPDI) were performed using 13C-NMR spectroscopy in solution. Chemical functions such as urethane, urea, allophanate, and biuret were all expected to be detected in these polymeric binders. 13C-NMR assignment of the C—O urethane and urea functions were found in these polymers as determined by using model compounds of IPDI. The 13C-NMR data gathered in this article can be considered as basic parameters for further characterization of polyurethane structure based on IPDI. Also, 13C CP MAS NMR spectra of GAP-IPDI-based polymers were carried out to identify the various chemical functions present in solid polyurethane elastomer. In addition, the curing evolution of a GAP-IPDI-based polymer at 50 and 80°C in bulk was monitored, and the reaction path of the binder was readily determined. Some conclusions on the effects of the cure catalyst and the curing temperature were also drawn. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35: 2991-2998, 1997
    Additional Material: 5 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 58 (1995), S. 827-834 
    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 bulk polymerization of hydroxyl-terminated polybutadene with tolylene diisocyanate has been studied in uncatalyzed isothermal reactions. The conversion in urethane was monitored by 13C-NMR spectroscopy of the C=O function at level up to 70%. Effects of reagents ratio and temperature were investigated. The experimental data were modeled by a set of two competitive second-order reactions to account for the difference in reactivity of o-NCO and p-NCO groups of tolylene 2,4 diisocyanate. The apparent kinetic constants calculated appeared to be statistically higher than previous results found in literature from work in aromatic solvents. Deviations from second-order law were observed during the last stage of polymerization. Activation energies were estimated at 12.3 kJ. mol-1 and 42.8 kJ. mol-1 for the p-NCO and o-NCO groups, respectively. The difference in their reactivity tended to decrease as temperature of reaction was increased. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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