Journal of Polymer Science Part B Polymer Physics · 2002 · 204 citations · 24 references
Natural SciencesMaterials EngineeringMaterials SciencePolymer ChemistryPolymer EngineeringPolymer MaterialsPolymer BlendsPolymer CharacterizationPolymer CrystallinityPolymer CrystallizationPolymer Phase BehaviorThermoplastic PolymersBlend ThermodynamicsCrystallizationCrystallization BehaviorCrystallization In BlendsMiscible Polymer BlendsPoly(lactic Acid)Polymer Blend ThermodynamicsThermodynamics Of Polymer Blends
Abstract Blends of amorphous poly(DL‐lactide) (DL‐PLA) and crystalline poly(L‐lactide) (PLLA) with poly(methyl methacrylate) (PMMA) were prepared by both solution/precipitation and solution‐casting film methods. The miscibility, crystallization behavior, and component interaction of these blends were examined by differential scanning calorimetry. Only one glass‐transition temperature ( T g ) was found in the DL‐PLA/PMMA solution/precipitation blends, indicating miscibility in this system. Two isolated T g 's appeared in the DL‐PLA/PMMA solution‐casting film blends, suggesting two segregated phases in the blend system, but evidence showed that two components were partially miscible. In the PLLA/PMMA blend, the crystallization of PLLA was greatly restricted by amorphous PMMA. Once the thermal history of the blend was destroyed, PLLA and PMMA were miscible. The T g composition relationship for both DL‐PLA/PMMA and PLLA/PMMA miscible systems obeyed the Gordon–Taylor equation. Experiment results indicated that there is no more favorable trend of DL‐PLA to form miscible blends with PMMA than PLLA when PLLA is in the amorphous state. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 23–30, 2003
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