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Glass transition temperatures, for

Other Properties. The glass-transition temperature for PPO is 190 K and varies htde with molecular weight (182). The temperature dependence of the diffusion coefficient of PPO in the undiluted state has been measured (182). [Pg.355]

The Arrhenius equation holds for many solutions and for polymer melts well above their glass-transition temperatures. For polymers closer to their T and for concentrated polymer and oligomer solutions, the WiUiams-Landel-Ferry (WLF) equation (24) works better (25,26). With a proper choice of reference temperature T, the ratio of the viscosity to the viscosity at the reference temperature can be expressed as a single universal equation (eq. 8) ... [Pg.170]

Polymers of Styrene Derivatives. Many styrene derivatives have been synthesized and the corresponding polymers and copolymers prepared (61). Glass-transition temperatures for a series of substituted styrene polymers are shown in Table 3. The highest T is that of... [Pg.507]

For many polymers it has been found that C1 and C2 are constants and Tref is taken asT, the glass transition temperature for the polymer (values are given in Table 1.8). The WLF equation then takes the form... [Pg.117]

The advantage of the simulations compared to the experiments is that the correspondence between the tracer diffusion coefficient and the internal states of the chains can be investigated without additional assumptions. In order to perform a more complete analysis of the data one has to look at the quench-rate and chain-length dependence of the glass transition temperature for a given density [43]. A detailed discussion of these effects is far beyond the scope of this review. Here we just want to discuss a characteristic quantity which one can analyze in this context. [Pg.502]

Table IV. Influence of Graft Molecular Weight on Glass Transition Temperature for PMMA-g-PSX Copolymers ( 16 wt.% PSX)... Table IV. Influence of Graft Molecular Weight on Glass Transition Temperature for PMMA-g-PSX Copolymers ( 16 wt.% PSX)...
The polybutadienes prepared with these barium t-butoxide-hydroxide/BuLi catalysts are sufficiently stereoregular to undergo crystallization, as measured by DTA ( 8). Since these polymers have a low vinyl content (7%), they also have a low gl ass transition temperature. At a trans-1,4 content of 79%, the Tg is -91°C and multiple endothermic transitions occur at 4°, 20°, and 35°C. However, in copolymers of butadiene (equivalent trans content) and styrene (9 wt.7. styrene), the endothermic transitions are decreased to -4° and 25°C. Relative to the polybutadiene, the glass transition temperature for the copolymer is increased to -82°C. The strain induced crystallization behavior for a SBR of similar structure will be discussed after the introduction of the following new and advanced synthetic rubber. [Pg.82]

Figure 11. The effect of reflow nearby the glass transition temperature for a PMMA-DR1 waveguide (a) device structure, (b) SEM picture of waveguide before reflow, (c) idem after reflow. Figure 11. The effect of reflow nearby the glass transition temperature for a PMMA-DR1 waveguide (a) device structure, (b) SEM picture of waveguide before reflow, (c) idem after reflow.
Also termed glass temperature or Tg. The temperature at which the stiffness of an elastomer subjected to low temperatures changes most rapidly. If the glass temperature is close to the operational temperature the material will be leathery in its behaviour rather than rubber-like. Approximate glass transition temperatures for different polymers are NR -70 °C SBR -52 °C HR -75 °C PCP -40 °C and silicone rubber -85 °C. [Pg.31]

In contrast to the mature instrumental techniques discussed above, a hitherto nonexistent class of techniques will require substantial development effort. The new instruments will be capable of measuring the thermal (e.g., glass transition temperatures for amorphous or semicrystalline polymers and melting temperatures for materials in the crystalline phase), chemical, and mechanical (e.g., viscoelastic) properties of nanoscale films in confined geometries, and their creation will require rethinking of conventional methods that are used for bulk measurements. [Pg.146]

To illustrate this more quantitatively, consider the hypothetical sucrose example discussed by Ahlneck and Zografi [80]. Assuming that all the sorbed water is taken up by the amorphous portion of material, 0.1% total moisture would correspond to approximately 20%, 10%, 4%, and 2% moisture content in the amorphous material, respectively, for 0.5%, 1%, 2.5%, and 5% of amorphous solid. The glass transition temperatures for the amorphous portions... [Pg.413]

D.F. O Brien, P.E. Burrows, S.R. Forrest, B.E. Koene, D.E. Loy, and M.E. Thompson, Hole transporting materials with high glass transition temperatures for use in organic light-emitting devices, Adv. Mater., 10 1108-1112 (1998). [Pg.398]

As films, certain polyimides remain functional at cryogenic temperatures, -269°C for example. Typical glass transition temperatures for polyimides are 300°C and above. [Pg.590]

Although polymers exhibit both viscous and elastic responses at all temperatures, the elastic response is particularly strong at temperatures less than 50°C above the glass transition temperature, particularly for polymers well above their critical molecular weight. Polymers are often considered to have dominant viscous rheological responses if they are stressed at temperatures over 100 °C above the glass transition temperature for amorphous polymers or 100°C above the crystalline melting point for semicrystalline resins. [Pg.63]

Fig. 19 Glass-transition temperatures for the chain extended and the diblock copoly(2-oxazoline)s (the error bars represent the range of standard deviation). NonsoNonso, NonsoPheso, and PhesoNonso did not exhibit a glass transition temperature (Tg). The stars represent the literature values for MesoMeso, Et5oEt5o, and NonsoNonso, respectively. (Reprinted with permission from [90]. Copyright (2005) American Chemical Society)... Fig. 19 Glass-transition temperatures for the chain extended and the diblock copoly(2-oxazoline)s (the error bars represent the range of standard deviation). NonsoNonso, NonsoPheso, and PhesoNonso did not exhibit a glass transition temperature (Tg). The stars represent the literature values for MesoMeso, Et5oEt5o, and NonsoNonso, respectively. (Reprinted with permission from [90]. Copyright (2005) American Chemical Society)...
The mobility of the ions in polymer electrolytes is linked to the local segmental mobility of the polymer chains. Significant ionic conductivity in these systems will occur only above the glass transition temperature of the amorphous phase, Tg. Therefore, one of the reqnirements for the polymeric solvent is a low glass-transition temperature for example, Tg = —67°C for PEO. [Pg.589]


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Glass Transition Temperature for Selected

Glass Transition Temperature for Selected Polymers

Transition temperature for

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