Polymer-diluent mixtures poly

In analyzing polyethylene-diluent mixtures it was noted that for certain diluents and concentrations the melting temperature remained invariant with composition. This is not an isolated observation. Besides linear polyethylene, this phenomenon has also been observed in long chain branched polyethylene,(21) poly(chlorotrifluoroethylene),(22) poly(N,N -sebacoyl piperazene),(23) isotactic poly(propylene),(24) and poly (acrylonitrile) (25) when the polymers are admixed... 

Fig. 3.9 Plot of melting temperatures against volume fractions of polymers for mixtures of poly(N,N sebacoyl piperazine) with different diluents. Diphenyl ether O < -nitrotoluene...

An analysis of the overall crystallization rate with composition requires that the comparison be made either at constant undercooling or at one of the nucleation temperature quantities, T / T AT or T /T(AT). This requirement is essential because of the importance of nucleation to the crystallization process. The overall crystallization kinetics of a variety of polymer-diluent systems have been reported. Many different relations between the overall crystallization rate and composition have been observed. For example, as is shown in Fig. 13.17 there is a continuous decrease in the crystallization rate with dilution for linear polyethylene-a-chloronaphthalene mixtures.(42) The results for poly(trans-1,4-isoprene) in methyl oleate follow a similar pattem.(80) In contrast, the rates for poly(dimethyl siloxane) crystallizing from toluene, at compositions V2 = 0.32 to 0.79, are the same at all undercoolings, but are faster than that of the pure polymer.(78) Another example is found with poly(ethylene oxide)-diphenyl ether mixtures.(77) In this case the crystallization rates for the pure polymer and composition = 0.92 to 0.51 are the same. However, the rates for the more dilute mixtures, V2 = 0.04 and 0.30 are lower. For poly(decamethylene adipate)-dimethyl formamide mixture the rates for the pure polymer and V2 = 0.80 are the same.(77) The mixture of isotactic poly(propylene) with dotricontane shows interesting behavior.(81) At all undercoolings studied, the crystallization rate initially decreases with dilution, reaches a minimum in the range V2 — 0.7 (a maximum in ti/2) and then slowly increases with further dilution, up to V2 = 0.10. 

Polymers that show a rate maximum with respect to temperature in the pure state do so also when crystallizing from diluent mixtures.(42a,67,88) Two examples are shown in Figs. 13.32 and 13.33 for isotactic poly(styrene) crystallizing from ether benzophenone or dimethyl phthalate respectively.(42a,67) Characteristically, the addition of the diluent causes a shift of the crystallization range to lower temperatures. A similar effect was observed with bisphenol-A poly(carbonate).(88) In addition, the growth rate maximum increases with the initial addition of diluent. This phenomenon is observed up to about 20% diluent in the case of benzophenone (Fig. 13.32) and about 50% with dimethyl phthalate (Fig. 13.33). A similar pattern is also indicated for the poly(carbonate)-diluent mixture.(89) With further additions of diluent there is a continuous decrease in the growth maxima up to very dilute... 

Typical phase diagrams that illustrate these principles are presented in Fig. 3.8 for isotactic poly(propylene)-alky phenol mixtures (24) and in Fig. 3.9 for poly (N,N -sebacoyl piperazine) (23) with various diluents. At the higher isotactic poly (propylene) compositions only liquid-solid curves are observed that result in typical melting temperature depression. Although at lower polymer concentrations... 

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