4.7 Article

Nanoconfined Crystallization in Poly(lactic acid) (PLA) and Poly(ethylene terephthalate) (PET) Induced by Various Forms of Premelt-Deformation

Journal

MACROMOLECULAR RAPID COMMUNICATIONS
Volume 44, Issue 1, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/marc.202200293

Keywords

ductility; melt-shear deformation; nanoconfined crystallization; processing-structure-property relationship; semicrystalline polymers

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The processing-structure-property relationship of poly(lactic acid) (PLA) and poly(ethylene terephthalate) (PET) is investigated. Pre-extension and preshear of amorphous PLA and PET above their glass transition temperatures induce nanoconfined crystallization (NCC) during annealing, resulting in optically transparent materials. The structural changes after premelt deformation greatly enhance the mechanical properties of the materials.
The processing-structure-property relationship using poly(lactic acid) (PLA) and poly(ethylene terephthalate) (PET) is explored. Specifically, both pre-extension and preshear of amorphous PLA and PET above their glass transition temperatures T-g, carried out in the affine deformation limit, can induce a specific type of cold crystallization during annealing, i.e., nanoconfined crystallization (NCC) where crystal sizes are limited to a nanoscopic scale in all dimensions so as to render the processed PLA and PET optically transparent. The new polymer structure after premelt deformation can show considerably enhanced mechanical properties. For example, premelt stretching produces geometric condensation of the chain network. This structural alternation can profoundly change the mechanical characteristics, e.g., turning brittle PLA ductile. In contrast, after preshear of amorphous PLA above T-g, the NCC containing PLA remains brittle, showing the importance to have geometric condensation from processing. Both AFM imaging and SAXS measurements are performed to verify that premelt deformation of PLA and PET indeed results in NCC from annealing that permits the strain-induced cold crystallization to take place on the length scale of the mesh size of the deformed chain network.

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