Phase morphology of iPP/aPS/SEP blends

• Published in: European polymer journal 2004-07, Vol.40 (7), p.1433-1443
• Main Authors: SMIT, I, RADONJIC, G, HLAVATA, D
• Format: Article
• Language: English
• Subjects: Applied sciences; Exact sciences and technology; Morphology; Organic polymers; Physicochemistry of polymers; Polymer blends; Polypropylene; Polystyrene; Properties and characterization; SEP diblock copolymer; Structure, morphology and analysis
• ISSN: 0014-3057; 1873-1945
• DOI: 10.1016/j.eurpolymj.2004.02.002

Supermolecular structure and phase morphology of the ternary isotactic polypropylene/atactic polystyrene/poly(styrene- b-ethylene- co-propylene) (iPP/aPS/SEP) compression molded blends with 100/0, 90/10, 70/30, and 50/50 iPP/aPS weight ratios and with different amounts of added SEP compatibilizer were studied by optical microscopy (OM), scanning electron microscopy (SEM), transmission electron microscopy (TEM), small-angle X-ray scattering (SAXS) and wide-angle X-ray diffraction (WAXD). SEP significantly reduced the size of dispersed aPS particles that enabled better spherulitization in the iPP matrix. Furthermore, iPP spherulites in ternary blends with 90/10 iPP/aPS weight ratio became larger in comparison with the pure iPP. TEM revealed that the SEP formed continuous interface layer around the dispersed aPS particles even when only 2.5 wt.% of SEP was added. Particle size distribution was distinctly bimodal. When the SEP content was increased to 10 wt.%, joining together smaller and bigger aPS and SEP particles formed dispersed aggregates. Additionally, both amorphous components (aPS and SEP) influenced crystallization process of iPP matrix and so modified, to some extent, its final supermolecular structure. SEP compatibilizer did not significantly affect crystallite orientation. The increase of crystallite sizes, which was more affected by the addition of aPS than by the addition of SEP, seemed to be influenced by the solidification effect rather than by the phase morphology of the blends.