Abstract

Viscosity measurements are made on aqueous borax solutions of poly(vinyl alcohol) (PVA) samples over a wide range of PVA concentration, C, to examine the hydrodynamic properties of associated polymers compared to those of neutral polymers. The dynamic viscoelastic data are reanalyzed using a statistical−mechanical theory for elastically effective chains in transient gels developed by Tanaka and Ishida. The viscosity data are not superposed in the plot of viscosity against C[η] using the Huggins relationship, especially around and over a critical concentration, CN, at which the dynamical behaviors drastically change and an inflection point of a curve in the plot of the viscosity against C is located. On the other hand, when we assume that the chain dimension around CN is the unperturbed one, the viscosity data around CN is well-superposed on a curve in the plot of viscosity against C/C*up, where C*up is the overlapping concentration of the unperturbed chain. The inflection point of this composite curve is ...

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