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  • Artikel: DFG Deutsche Nationallizenzen  (3)
  • 1995-1999  (1)
  • 1985-1989  (2)
  • 1965-1969
  • Polymer and Materials Science  (3)
Datenquelle
  • Artikel: DFG Deutsche Nationallizenzen  (3)
Materialart
Erscheinungszeitraum
  • 1995-1999  (1)
  • 1985-1989  (2)
  • 1965-1969
  • 1980-1984  (2)
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 1367-1375 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A pair of aliphatic amines were synthesized in order to study the effect steric hindrance has on the physical properties of an amine-cured epoxy resin. The hindered amine (TMSiDA) has NH2 groups that are obstructed by the presence of adjacent methyl groups while the unhindered amine (SiDA) does not contain any NH2 steric hindrance. DGEBA cured with TMSiDA is less dense, absorbs less moisture, and has a higher Tg than does SiDA/DGEBA. Torsional pendulum results show that TMSiDA/DGEBA has a slightly higher rubbery modulus and a secondary transition at a lower temperature than DGEBA cured with SiDA. Activation energies for the secondary transition were determined for TMSiDA/DGEBA and SiDA/DGEBA and are 19 and 14 kcal/mol, respectively.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 1829-1852 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Measurements were made of the thermal and dynamic mechanical properties of 22 polyurethaneureas of varying diol molecular weight, type of aromatic chain extender, diol molecular weight distribution, and chain extender stoichiometry. The dynamic mechanical data, obtained as a function of temperature and frequency (in the kHz region), were used to construct master curves of shear modulus and loss factor over a wide range of reduced frequencies. Based on these master curves, interpreted in conjunction with the thermal analysis results, it was found that: Soft segment crystallization occurs at the higher diol molecular weights, dynamic mechanical properties are well correlated with the soft segment glass transition, diol molecular weight influences dynamic mechanical properties by affecting the degree of phase separation and hence glass transition temperature, and neither diol molecular weight distribution nor chain extender stoichiometry have a significant effect, in the ranges studied, on transition temperatures or dynamic mechanical properties.
    Zusätzliches Material: 25 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 1985-1993 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: The method of additive properties was used to calculate the dynamic mechanical relaxation time for a series of polyurethanes. Calculations were also made of density and glass transition temperature. Group contributions for nine component groups were determined. With these group values, the densities of the 12 polymers used to determine the groups were calculated and found to agree with measured values within an average of 0.2%. Calculated glass transition temperatures also agreed with measured values within 0.2%. The relaxation time, defined as a parameter in the Havriliak-Negami equation, was shown to be correlated with the glass transition temperature, allowing relaxation time to also be expressed as an additive property. Calculated logarithms of relaxation times agree with measured values to within 7% over a range of relaxation times covering many decades. © 1996 John Wiley & Sons, Inc.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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