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ABSTRACT The crystallization of polypropylene with different density of macromolecular entanglements was studied in isothermal and non-isothermal conditions. The growth rate of spherulites increased with reduced concentration of entanglements. Reduction of entanglements shifted the temperature of transition between Regimes II and III, which means that more regular growth of crystals was possible at lower temperature. The range of temperatures at which polypropylene cavitated in regions of melt occluded by spherulites was limited to 137-139°C, with weak dependence on entanglements density. DSC studies showed that isothermal crystallization is faster in less entangled polymers, however the crystallinity degree and long period of structure (by SAXS) were similar for studied materials. When the crystallization was completed during fast cooling, the differences between individual samples were more significant. The partial disentangling, overcoming some limitation for movements of macromolecules, made possible easier crystallization, even at low temperature of Regime III. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2017, 55, 748-756 [ABSTRACT FROM AUTHOR]

ABSTRACT Coefficients of linear thermal expansion (CTE) for poly(propylene)/ poly(propylene)-grafted-maleic anhydride/montmorillonite ethylene-co-octene elastomer (PP/PP-g-MA/MMT/EOR) blend nanocomposites were determined as a function of MMT content and various PP-g-MA/organoclay masterbatch ratios. The nanocomposites were prepared in a twin-screw extruder at a fixed 30 wt % elastomer, 0-7 wt % MMT content, and various PP-g-MA/organoclay ratio of 0, 0.5, 1.0, and 1.5. The organoclay dispersion facilitated by the maleated PP helps to reduce the size of the dispersed phase elastomer particles in the PP matrix. The elastomer particle size decreased significantly as the PP-g-MA/organoclay ratio and MMT content increased; the elastomer particles viewed // to flow direction (FD) are smaller and less deformed compared to those viewed // to transverse direction (TD). The elastomer particle shape based on the view along the three orthogonal directions of the injection molded sample is similar to a prolate ellipsoid. The CTE decreased significantly in the FD and TD, whereas a slight increase is observed in the normal direction in the presence of MMT and PP-g-MA. The Chow model based on a two population approach showed better fit to experimental CTE when the effect of MMT and elastomer are considered individually. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B Polym. Phys. 2013, 51, 952-965 [ABSTRACT FROM AUTHOR]

ABSTRACT The deformation behavior of a polypropylene (PP) sheet, in which c-axis of β-form PP orients perpendicular to the flow direction in the sheet [transverse direction (TD)], is studied focusing on the mechanical anisotropy. The deformation mechanism of this sample is found to be strongly dependent on the stretching direction. Shear yielding is dominant in TD stretching, indicating that reorganization and phase transformation of crystalline form occur easily with low yield stress. On the contrary, in machine direction (MD) stretching, numerous microvoids appear with the transformation of crystalline form as well as the rotation of c-axis. Moreover, the crazing process, initiated at the orientation defects, occurs locally with remaining undeformed region in which β-form PP orients to TD. The deformation behavior is applicable to a microporous film. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2013, 51, 897-906 [ABSTRACT FROM AUTHOR]