Comparative studies on miscibility and phase behavior of linear and star poly(2-methyl-2-oxazoline) blends with poly(vinylidene fluoride)

• Published in: Journal of polymer science. Part B, Polymer physics Polymer physics, 2006-03, Vol.44 (6), p.942-952
• Main Authors: Shen, Jia, Zheng, Sixun
• Format: Article
• Language: English
• Subjects: Applied sciences; Exact sciences and technology; miscibility; Organic polymers; Physicochemistry of polymers; poly(2-methyl-2-oxazoline); poly(vinylidene fluoride); polyhedral oligomeric silsesquioxane; Properties and characterization; star-shaped polymer; Thermal and thermodynamic properties
• ISSN: 0887-6266; 1099-0488
• DOI: 10.1002/polb.20748

The comparative studies on the miscibility and phase behavior between the blends of linear and star‐shaped poly(2‐methyl‐2‐oxazoline) with poly(vinylidene fluoride) (PVDF) were carried out in this work. The linear poly(2‐methyl‐2‐oxazoline) was synthesized by the ring opening polymerization of 2‐methyl‐2‐oxazoline in the presence of methyl p‐toluenesulfonate (MeOTs) whereas the star‐shaped poly(2‐methyl‐2‐oxazoline) was synthesized with octa(3‐iodopropyl) polyhedral oligomeric silsesquioxane [(IC3H6)8Si8O12, OipPOSS] as an octafunctional initiator. The polymers with different topological structures were characterized by means of Fourier transform infrared spectroscopy and nuclear magnetic resonance spectroscopy. It is found that the star‐shaped poly(2‐methyl‐2‐oxazoline) was miscible with poly(vinylidene fluoride) (PVDF), which was evidenced by single glass‐transition temperature behavior and the equilibrium melting‐point depression. Nonetheless, the blends of linear poly(2‐methyl‐2‐oxazoline) with PVDF were phase‐separated. The difference in miscibility was ascribed to the topological effect of PMOx macromolecules on the miscibility. © 2006 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 942–952, 2006