Abstract

Using oscillatory and steady-shear rheometry on polystyrene (PS) solutions in tricresyl phosphate (TCP) with three nearly monodisperse molecular weights at six values of the reduced concentration c/ce, where ce is the entanglement concentration, we show that for each value of c/ce below 2.0 rheological functions are successfully superimposed using de Gennes “blob” scaling laws for the concentration-dependent plateau modulus GN0, and the equilibration time τe,scaling using the literature value of the solvent-quality exponent ν = 0.53 (Solomon, M. J.; Muller, S. J. J. Polym. Sci., Polym. Phys. 1996, 334, 181−192). However, once the polymer volume fraction exceeds the “swelling volume fraction” ϕs, above which the polymer takes a random walk configuration on all length scales even in a good solvent, this universal scaling breaks down and the polymer conformation appears to be governed by Colby−Rubinstein’s scaling laws for Θ solutions. We estimate that all polybutadiene solutions in phenyl octane (a good sol...

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