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Influence of the β‐crystalline phase on the mechanical properties of unfilled and calcium carbonate‐filled polypropylene: Ductile cracking and impact behavior
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Citations
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References
2001
Year
EngineeringMechanical EngineeringImpact BehaviorSoft Matterβ CrystalsPolymersPolymer MaterialPolymer ProcessingPolymer ChemistryMaterials ScienceMechanical BehaviorPolymer EngineeringSolid MechanicsMaterial MechanicsPlasticityβ‐Crystalline FormIsotactic PolyMacromolecular ScienceMechanical PropertiesPolymer SciencePolymer Propertyβ‐Crystalline PhaseMechanics Of Materials
Abstract The β‐crystalline form of isotactic poly(propylene) (PP) has been long recognized to have a greater mechanical absorption capacity than the α‐crystalline form. This is of major importance for improving impact properties and crack resistance of injection‐molding parts. Unfilled PP samples together with calcium carbonate‐filled PP samples having various β/α‐phase ratios, with nearly constant morphological parameters, have been investigated from the standpoint of ductile crack propagation and impact behavior. The presence of the β‐crystalline phase turned out to improve both properties. The β spherulites are notably more prone to craze initiation than α spherulites that display a propensity for cracking. Subsequent crack propagation appears to be faster in the latter ones. The plastic zone ahead from the crack tip broadens, and the specific plastic energy increases with increasing β‐phase content. The lower elastic limit of the β phase is likely to promote the early crazing. However, the suspected higher density of tie molecules in β spherulites provides more numerous and stiffer microfibrils. The impact strength of PP is also improved by the presence of β crystals as a result of greater energy‐absorption capabilities. However, filled samples turned out insensitive to the β phase. A discussion is made about the origins of the β‐phase‐induced improvement of the mechanical properties. The possible role of the β → α transition is also explained. © 2001 John Wiley & Sons, Inc. J Polym Sci Part B: Polym Phys 40: 31–42, 2002
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