Fractionated crystallization isotactic polypropylene

In order to illustrate the fractionated crystallization behavior we will present here previous results on immiscible atactic PS and isotactic polypropylene blends (iPP) [68]. The cooling behavior of PS, iPP and an 80/20 PS/iPP blend is presented in Fig. 1, as well as that of an unmixed blend , labeled... 

Amer and van Reenen [39] fractionated isotactic polypropylenes by TREE to get fractions with different molar masses but similar tacticities. The DSC results of the fractions indicated that the crystallization behaviour is strongly affected by the configuration (tacticity) and the molar mass of the PP. Soares et al. [40] proposed a new approach for identifying the number of active catalyst sites and the polymer chain microstructural parameters produced at each active site for ethylene/l-olefin copolymers synthesized with multiple-site catalysts. This method is based on the simultaneous deconvolution of bivariate MMD/CCD, which can be obtained by cross-fractionation techniques like SEC/TREE or TREE/SEC. The proposed approach was validated successfully with model ethylene/1-butene and ethylene/ 1-octene copolymers. Alamo and co-workers [41] studied the effects of molar mass and branching distribution on mechanical properties of ethylene/1-hexene copolymer film grade resins produced by a metallocene catalyst Molar mass fractions were obtained by solvent/non-solvent techniques while P-TREE was used for fractionation according to the 1-hexene content. 

It is known the case of i-PP, for which the copolymerization with small amounts of ethylene tends to stabilize the y form [84] for instance, by melt crystallization of a copolymer with 6% by mol of ethylene more than 80% of the crystalline phase is in the y form [85], It is also known that the obtainment of the y form by melt crystallization, is also favored for samples of low molecular mass [86, 87] and for stereoblock fractions [88]. This seems to suggest that, whenever the preferential crystallization of the y-form is observed, there is the concomitant occurrence of a reduction in the polymer of the length of the chain stretches with polypropylene head to tail constitution and isotactic configuration. 

Isotactic and syndiotactic polymers can crystallize, while atactic polymers cannot. Polymers other than polypropylene that have tacticity include polystyrene, polyfvinyl chloride), and poly(methyl methacrylate). Thus there are crystalline and non-crystalline forms of these polymers. By use of a copolymer, the number of side groups, and thus the crystallinity can be precisely controlled. An important example is the copolymerization of ethylene and a higher alpha-olefin, such as butene or octane, to make linear low-density polyethylene (LLDPE), in which the crystallinity is governed by the fraction of comonomer incorporated into the chain. Tacticity can affect important physical properties such as the intrinsic viscosity and thus must be taken into accoimt in characterization methods such as gel permeation chromatography. 

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