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  • 1990-1994  (3)
Materialart
Erscheinungszeitraum
  • 1990-1994  (3)
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 23 (1990), S. 3687-3695 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 1127-1135 
    ISSN: 0887-6266
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Dielectric properties measured during isothermal curing of DGEBA-based thermosets using a mixture of aromatic amines as curing agent are analyzed. The evolution of the dielectric features of thermosets during curing and after a time when their dc conductivity has reached a negligibly small value are phenomenologically similar to the dielectric features of physically and chemically stable dipolar liquids and solids observed with increasing frequency or decreasing temperature. This equivalence is a consequence of the invariance of the dynamic behavior of dielectric susceptibility with respect to either the frequency of measurement or the relaxation time of the substance and demonstrates that crosslinking of a thermoset causes its relaxation time to increase monotonically.It is shown that the stretched exponential relaxation function formalism satisfactorily describes the dielectric results and that the value of its distribution parameter initially decreases and, after gelation, reaches a constant value, which we denote γ, in the latter part of the cure. The value of the curing parameter, γ, which lies between 0.2 and 0.4, monotonically decreases with increasing curing temperature and tends to a limiting value characteristic of a thermoset at higher temperatures. This is in contrast with the increase found in the corresponding representation in the Kohlrausch-Williams-Watts parameter β with increasing temperature. The curing time dependence of the dipolar relaxation time ι has been determined and found to have the shape of an elongated S, with a well-defined point of inflexion, as ι increases during the cure, from a value characteristic of a liquid to an ultimate value characteristic of a glass.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 29 (1991), S. 1117-1125 
    ISSN: 0887-6266
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The results obtained during the isothermal curing of diglycidyl ether of bisphenol-A-based thermosets cross-linked with pure diaminodiphenyl methane and pure diaminodiphenyl sulfone and with their mixtures have been analyzed to determine how the dc conductivity changes with time during the conversion of its liquid to a gel. The complex permittivity data are first analyzed to show that ac measurements can be used to obtain the ionic conductivity over a considerable period of the curing process. The procedure allows one to obtain the dc conductivity without having data as a function of frequency. The shape of the complex plane plots of the electrical modulus are semicircles, but with small deviations that appear at long times during the curing process. The dielectric consequences of the chemical changes with time during the cross-linking of the thermoset are analogous to the frequency dependence of the complex permittivity of a liquid. The analysis shows that the dc conductivity σo of a thermoset during its cure follows a power law, σo∝ (tg - t)x, where t is the curing time (t 〈 tg). The results can also be described equally well by a new equation, σo ∝ exp[ - B/(to - t)], where x, tg, B, and to are empirical constants all of which vary with the temperature of the cure. tg is close to the time for gelation known from independent studies and to is close to but longer than the time for vitrification. These conclusions are discussed in terms of scaling concepts for the gelation phenomenon.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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