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Nonlinear Influence of Blending Star and Triblock Copolymers on Morphological and Mechanical Properties of
Max G Schußmann1, Leonardo Rocha Dias1, Simon Buchheiser2
1Institute for Chemical Technology and Polymer Chemistry, Karlsruhe Institute of Technology (KIT), Engesserstraße 18, 76131, Karlsruhe, Germany.
Abstract:
To tune the mechanical properties of thermoplastic elastomers, a linear Poly(styrene (S)-b-isoprene (I)-b-styrene (S)) triblock copolymer (SIS) is blended with well-defined symmetric star-shaped PS-PI block copolymers with 8 and 15 arms, respectively. The model systems are synthesized via anionic polymerization and grafting-onto techniques and have a lamellar morphology with the long-range order L0 for the SIS larger than the stars. Morphological analysis using small angle X-ray scattering (SAXS) and atom force microscopy (AFM) reveals a nonlinear dependency of L0 as a function of the star content, ϕstar. For small star contents, L0 of the blends increases above L0 of the individual compounds. The stars show significantly higher mechanical performance than the SIS, by an increased elongation at break, εb, by +15% and +38%, and an increased ultimate tensile strength, σUTS, by about a factor of 2. For the blends, the mechanical properties highly depend on the star content, and can be fully uncoupled from the ones of the SIS and the star: at small star contents εb is significantly improved beyond εb,star, but σUTS decreases below σUTS,SIS. For higher star contents, σUTS strongly increases toward σUTS,star , whereas εb shows a minimum around ϕstar = 50 wt.%, before increasing to εb,star.
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