Journal of Applied Polymer Science · 1979 · 21 citations · 6 references
Natural SciencesMaterials EngineeringMaterials ScienceCrystal StructureMaterials CharacterizationMechanical Behavior Of MaterialsCrystallization ProcessesCrystallographyDeformation MechanismsDislocation MechanicsPlastic DeformationX-ray CrystallographyChainsCrystal PlasticityDeformationMolecular OrientationMorphological TransitionsPolypropylene
Abstract The strains on uniaxial extension of preoriented isotactic polypropylene are separated over the whole range of deformation into three processes: crystallite boundary slip (A 1 process), uniform shear deformation of crystallites (A 2 process), and restoration of molecular orientation from the sheardeformed state (Ā 2 process). They are separately evaluated by the use of the parameters of superstructure varying in deformation. Both the A 1 and A 2 processes predominate before the A 2 → Ā 2 transition takes place. Wide‐ and small‐angle x‐ray goniometries detect this transition. After the A 2 → Ā 2 transition takes place, the specimen cannot be deformed by the A 1 or A 2 process, but by a molecular process such as pulling out the isolated extending chains from the folded chain crystals followed by their refolding. From the quantitative evaluations of the strains associated with the A 1 and A 2 processes it is deduced that the initial shear compliance for the A 1 process is smaller than that for the A 2 process.
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