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Entanglement density poly

Fig. 3. Critical strain intensity factor versus entanglement density for various polymers (filled squares data taken from [13] open squares this study), a polystyrene b poly(methyl methacrylate) c poly(vinyl chloride) d polyamide 6 e polyoxymethylene f bisphenol-A polycarbonate g poly(ethylene terephthalate) h SAPA-A series i SAPA-R series. Fig. 3. Critical strain intensity factor versus entanglement density for various polymers (filled squares data taken from [13] open squares this study), a polystyrene b poly(methyl methacrylate) c poly(vinyl chloride) d polyamide 6 e polyoxymethylene f bisphenol-A polycarbonate g poly(ethylene terephthalate) h SAPA-A series i SAPA-R series.
Figure 10.3 Mean molecular mass between chemical crosslinks and trapped chain entanglements Mc+e in a cured mixture of a poly(ethylene glycol) diacrylate (PEGDA) and 2-ethylhexyl acrylate (EHA) as a function of the EHA content [52]. Mc+e values were determined from (1/T2s)max and the plateau modulus (see Figure 10.2). A substantial difference in Mc+e value, as determined by these two methods at low crosslink density, is caused by the effect of network defects which decrease volume average network density determined by DMA (see Section 10.3). The molecular mass of PEGDA (Mn = 700 g/mol) is indicated by an arrow. The molecular mass of network chains in cured PEGDA is about three times smaller than that of the initial monomer. The molecular origin of this difference is discussed in Section 10.3... Figure 10.3 Mean molecular mass between chemical crosslinks and trapped chain entanglements Mc+e in a cured mixture of a poly(ethylene glycol) diacrylate (PEGDA) and 2-ethylhexyl acrylate (EHA) as a function of the EHA content [52]. Mc+e values were determined from (1/T2s)max and the plateau modulus (see Figure 10.2). A substantial difference in Mc+e value, as determined by these two methods at low crosslink density, is caused by the effect of network defects which decrease volume average network density determined by DMA (see Section 10.3). The molecular mass of PEGDA (Mn = 700 g/mol) is indicated by an arrow. The molecular mass of network chains in cured PEGDA is about three times smaller than that of the initial monomer. The molecular origin of this difference is discussed in Section 10.3...
Ma and Tang (32) showed that increasing cross-link density of SINs of poly(n-butyl acrylate) and epoxy 10 90 compositions tends to increase molecular interpenetration, and thus entanglement between the two networks. [Pg.4070]

It has been shown that the viscoelastic losses of OH-terminated poly(dimethyl-siloxane), crosslinked with tetra-functional silicates, decreases with increased crosslink density. Furthermore, identical results were obtained when the polymer was crosslinked with y-irradiation, in bulk and in solution this indicates that there is no significant change in the number of interchain entanglements, and these are responsible for the observed losses. Vulcanization studies of poly(di-methylsiloxane)s, y-irradiated up to 500 Mrad, have shown linear correlation of the crosslink density with swelling, indentation and extension behaviour up to 160 Mrad, and exponentially for higher doses. Basic principles for the thermal stabilization of silicone rubbers, filled with carbon blacks and silica, have been discussed and a tentative stabilization mechanism put forward. ... [Pg.212]


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