455899 Polyolefin Toughened Polypropylene: Phase Behavior and Mechanical Properties

Thursday, November 17, 2016: 1:45 PM
Continental 3 (Hilton San Francisco Union Square)
Jun Xu, Department of Chemical Engineering and Material Science, University of Minnesota, Minneapolis, MN and Frank S. Bates, Department of Chemical Engineering and Materials Science, University of Minnesota, Minneapolis, MN

A series of poly(cyclohexylethylene-ran-ethylene) (CE) copolymers were synthesized with statistical segment lengths designed to match that of isotactic poly(propylene) (iPP). Melt blending the CE compounds containing 50% to 70% by weight cyclohexylethylene repeat units with iPP at loadings between 5 to 20 wt.% resulted in a dispersion of CE droplets with number average diameters between 150 and 400 nanometers as determined by scanning electron microscopy. Linear dynamic mechanical elastic (G¢) and loss (G¢¢) moduli data were fit to the Palierne model providing estimates for the interfacial tension between iPP and CE, which was interpreted based on enthalpic (χH) and entropic (χS) contributions to the overall segment-segment interaction parameter, χ = χH + χS, attributed to density and statistical segment length differences, respectively. The small particle sizes are explained by a reduced interfacial tension, driven by minimization of χS (» 0), counterbalanced by χH > 0, establishing an optimal balance between phase separation and dispersion during blending at practical molecular weights. The optically clear blends exhibit superior tensile mechanical properties, with the strain at break increasing from 20% for iPP to 400% at a loading of 5 wt%, attributable to shear yielding of the matrix triggered by cavitation of the uniformly dispersed CE copolymer particles.

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See more of this Session: Mechanics and Structure in Polymers
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