Factors affecting timecomposition equivalence in ternary block copolymer/cosolvent systems

Timetemperature rheological equivalence is one of the most important and broadly used concepts developed with regard to the viscoelastic behavior of polymers. In this study, we explore the generality of an analogous relationship, timecomposition equivalence, in several series of ternary block copolymer/cosolvent systems at ambient temperature. Of particular interest are triblock copolymers solvated with a miscible mixture of midblock-selective solvents to yield physical gels. Such gels, consisting of a midblock-rich network stabilized by glassy endblock-rich microdomains, exhibit remarkable elasticity. The copolymers employed here are styrenic thermoplastic elastomers, whereas the solvents include an aliphatic/alicyclic mineral oil and several different tackifying resins varying in molecular weight and, hence, viscosity. Despite changes in solvent properties, timecomposition superpositioning (tCS) yields master curves wherein the composition shift factors consistently scale with cosolvent zero-shear viscosity. Corresponding scaling exponents vary linearly with copolymer concentration and change slope at a morphological transition. Failure of tCS at low frequencies can be largely avoided by implementing copolymers with high-molecular-weight endblocks. Triblock copolymers exhibit timecomposition rheological equivalence in the presence of midblock-selective cosolvents differing substantially in viscosity. We explore several material factors governing such equivalence and establish its range of applicability.