Abstract
Formation of a stereocomplex structure in a blend of isotactic and syndiotactic poly(methyl methacrylate)s (iPMMA/sPMMA) was found to be significantly enhanced by introducing a mutual miscible diluent of poly(ethylene oxide) (PEO) in the blend, even when prepared using a kinetically hindered noncomplexing CHCl3 solvent. Mechanisms and influencing factors, such as thermal treatment, annealing temperature, annealing time, or PEO content in blends, on structures of stereocomplexes in the ternary iPMMA/sPMMA/PEO blends are discussed. WAXD result showed that addition of PEO in the iPMMA/sPMMA blend did not alter the crystal cells in the complexes. Melting peaks associated with the complexes were analyzed for discerning possible structural mechanisms. When annealed at specific temperatures, multiple endothermic peaks of the complexes increased in intensity as PEO contents increased in the ternary blends. Analysis shows that the lower melting peak (P1) represents shorter stereocomplex sequences or stereocomplex detached from PEO or connected with partial PEO, but the higher melting peak (P3) is related to the stereocomplex physically interconnected in the presence of PEO. The PEO molecules are thought to more easily interact with the stereocomplexes in blends by acting as a plasticizer, which decreases Tg of the more rigid PMMA chain segments. Physical interaction or miscibility-enhanced chain entanglement probably exists between PEO and the stereocomplex of tactic PMMAs, leading to stereocomplex formation in the iPMMA/sPMMA/PEO ternary blend. FT-IR characterization provided evidence of weak interactions between PEO and the stereocomplex of PMMA. IR peaks sensitive to complex structures with respect to temperature were analyzed for discerning effects by adding PEO. The stereocomplex formation of ternary blends with PEO is due to the weak interaction of ester groups and methoxy groups between PMMA and PEO.
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