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Epoxy glass transition temperature

Tg dry ( C) Film adhesives (Epoxy) Glass transition temperature, in °C, for product in a dry condition. [Pg.65]

Epoxy - Glass transition temperature Epoxy/MWCNT-NH2 - Glass transition temperature Epoxy/MWCNT - Glass transition temperature... [Pg.21]

The highly polar nature of the TGMDA—DDS system results in high moisture absorption. The plasticization of epoxy matrices by absorbed water and its effect on composite properties have been well documented. As can be seen from Table 4, the TGMDA system can absorb as much as 6.5% (by weight) water (4). This absorbed water results in a dramatic drop in both the glass transition temperature and hot—wet flexural modulus (4—6). [Pg.21]

The use of elastomeric modifiers for toughening thermoset resias generally results ia lowering the glass transition temperature, modulus, and strength of the modified system. More recendy, ductile engineering thermoplastics and functional thermoplastic oligomers have been used as modifiers for epoxy matrix resias and other thermosets (12). [Pg.23]

Urethane structural adhesives have a morphology that is inverse to the toughened epoxy just described. The urethanes have a rubber continuous phase, with glass transition temperatures of approximately —50°C. This phase is referred to as the .soft segment . Often, a discontinuous plastic phase forms within the soft segment, and that plastic phase may even be partially crystalline. This is referred to as the hard segment . A representation of the morphology is shown in Fig. 3 [34]. [Pg.773]

The two-component urethane structural adhesives are among the most difficult to characterize, simply because of the widely varying properties that are possible. These adhesives may be rigid plastics similar in modulus to standard epoxy adhesives, with glass transition temperatures of the cured adhesive being approximately 60°C. [Pg.795]

Adhesive strength is evaluated at room temperature as well as at the extreme temperatures of —65°F and 180°F. Aircraft structure can reach —65°F at cruise altitudes and 180°F on the ground in a hot, sunny location. The types of toughened epoxies commonly used for metal bond adhesives have glass transition temperatures not much greater than 200°F, so properties fall off drastically at higher temperatures. [Pg.1147]

Fig. 6. The variation of the heat capacity jumps at the respective glass transition temperatures versus inclusion-volume contents of iron-epoxy particulates of different diameters of inclusions. In the same figure is presented the variation of the coefficients X for the same composites and volume contents... Fig. 6. The variation of the heat capacity jumps at the respective glass transition temperatures versus inclusion-volume contents of iron-epoxy particulates of different diameters of inclusions. In the same figure is presented the variation of the coefficients X for the same composites and volume contents...
Fig. 14. The variation of the specific heat jumps at glass-transition temperatures of elacc-epoxy composites, versus the fiber volume content, uf. The values for the factor X and the mesophase, (uj and matrix, (nm) volume fractions, versus uf, as derived from the values of the respective AC, s are also plotted... Fig. 14. The variation of the specific heat jumps at glass-transition temperatures of elacc-epoxy composites, versus the fiber volume content, uf. The values for the factor X and the mesophase, (uj and matrix, (nm) volume fractions, versus uf, as derived from the values of the respective AC, s are also plotted...
Network properties and microscopic structures of various epoxy resins cross-linked by phenolic novolacs were investigated by Suzuki et al.97 Positron annihilation spectroscopy (PAS) was utilized to characterize intermolecular spacing of networks and the results were compared to bulk polymer properties. The lifetimes (t3) and intensities (/3) of the active species (positronium ions) correspond to volume and number of holes which constitute the free volume in the network. Networks cured with flexible epoxies had more holes throughout the temperature range, and the space increased with temperature increases. Glass transition temperatures and thermal expansion coefficients (a) were calculated from plots of t3 versus temperature. The Tgs and thermal expansion coefficients obtained from PAS were lower titan those obtained from thermomechanical analysis. These differences were attributed to micro-Brownian motions determined by PAS versus macroscopic polymer properties determined by thermomechanical analysis. [Pg.416]

Fig. 38. Glass transition temperature of epoxies prepared with cyclohexane via CIPS before and after the drying procedure... Fig. 38. Glass transition temperature of epoxies prepared with cyclohexane via CIPS before and after the drying procedure...

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See also in sourсe #XX -- [ Pg.100 ]

See also in sourсe #XX -- [ Pg.91 ]




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