Publication | Closed Access
Comparison of propylene/ethylene copolymers prepared with different catalysts
36
Citations
20
References
2006
Year
Macromolecular ChemistryEngineeringChemistryPolymersChemical EngineeringPolymer MaterialPolymer TechnologyMacromolecular EngineeringPolymer ProcessingHybrid MaterialsPolymer ChemistryMaterials ScienceHomogeneous Propylene/ethylene CopolymersPostmetallocene CatalystNanomanufacturingPolymer EngineeringCatalysisPolymer SciencePropylene/ethylene CopolymersExperimental Propylene/ethylene CopolymersFunctional MaterialsPolymer Synthesis
Abstract This study compared a series of experimental propylene/ethylene copolymers synthesized by a transition metal‐based, postmetallocene catalyst (xP/E) with homogeneous propylene/ethylene copolymers synthesized by conventional metallocene catalysts (mP/E). The properties varied from thermoplastic to elastomeric over the broad composition range examined. Copolymers with up to 30 mol % ethylene were characterized by thermal analysis, density, atomic force microscopy, and stress–strain behavior. The xP/Es exhibited noticeably lower crystallinity than mP/Es for the same comonomer content. Correspondingly, an xP/E exhibited a lower melting point, lower glass transition temperature, lower modulus, and lower yield stress than an mP/E of the same comonomer content. The difference was magnified as the comonomer content increased. Homogeneous mP/Es exhibited space‐filling spherulites with sharp boundaries and uniform lamellar texture. Increasing comonomer content served to decrease spherulite size until spherulitic entities were no longer discernable. In contrast, axialites, rather than spherulites, described the irregular morphological entities observed in xP/Es. The lamellar texture was heterogeneous in terms of lamellar density and organization. At higher comonomer content, embryonic axialites were dispersed among individual randomly arrayed lamellae. These features were characteristic of a copolymer with heterogeneous chain composition. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1651–1658, 2006
| Year | Citations | |
|---|---|---|
Page 1
Page 1