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Crystal Modifications and Thermal Behavior of Poly(<scp>l</scp>-lactic acid) Revealed by Infrared Spectroscopy
855
Citations
33
References
2005
Year
Crystal StructureEngineeringBulk PllaChemistryPolymersPolymer MaterialCrystal FormationPolymer ChemistryMaterials ScienceInfrared SpectroscopyThermal BehaviorPhysical ChemistryPlla SamplesPolymer AnalysisCrystallographyPolymer MeltCrystal ModificationsMacromolecular SciencePolymer SciencePolymer CharacterizationPolymer Property
Recently, the isothermal crystallization behaviors of poly(l‑lactic acid) (PLLA) from melt and glassy states were reported. The study aims to clarify the unusual infrared spectral differences observed during PLLA crystallization at different temperatures. This was investigated by TEM, WAXD, and FTIR analyses of PLLA samples crystallized at various temperatures. The analyses revealed a new α‑form crystal modification for PLLA annealed below 120 °C, characterized by loose 103 helical chain packing and lower thermal stability than the standard α form, which explains all experimental observations. Published in Phys.
Recently, we reported the isothermal crystallization behaviors of poly(l-lactic acid) (PLLA) from the melt and glassy states, respectively [J. Phys. Chem. B 2004, 108, 11514; Macromolecules 2004, 37, 6433]. Surprisingly, the quite different infrared (IR) spectral evolutions occur in the two crystallization processes at different temperatures in which the same crystal modification is expected to be formed. To clarify this unusual phenomenon, the crystal modifications and thermal behavior of PLLA samples prepared under different crystallization temperatures are investigated in detail by TEM, WAXD, and FTIR techniques. On the basis of the WAXD and IR data, a new crystal modification named the α form is proposed for the crystal structure of PLLA samples annealed at temperature below 120 °C. Such crystal modification with loose 103 helical chain packing is less thermally stable than the standard α form of PLLA. This assignment can explain all the experiment observations well. Other possible mechanisms for the IR spectral difference of bulk PLLA samples annealed at different temperatures are also discussed.
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