Rheological Study of Transient Networks with Junctions of Limited Multiplicity II. Sol/Gel Transition and Rheology

TL;DR

This study develops a theoretical model for transient gelation in telechelic polymers, explaining how rheological properties like relaxation time and viscosity change near the sol/gel transition, aligning well with experimental data.

Contribution

The paper introduces a comprehensive transient network theory incorporating superbridge effects and correlation among chains, providing new insights into gelation dynamics and rheology.

Findings

Relaxation time $ au$ is proportional to concentration deviation $\Delta$ near gelation.

Plateau modulus $G_{\infty}$ scales with $\Delta^3$, and zero-shear viscosity with $\Delta^4$.

Model accurately describes concentration dependence of dynamic moduli in aqueous telechelic PEO solutions.

Abstract

Viscoelastic and thermodynamic properties of transient gels formed by telechelic polymers are studied on the basis of the transient network theory that takes account of the correlation among polymer chains via network junctions. The global information of the gel is incorporated into the theory by introducing the elastically effective chains according to the criterion by Scanlan and Case. We also consider effects of superbridges whose backbone is formed by several chains connected in series with several breakable junctions inside. Near the critical concentration for the sol/gel transition, superbridges becomes infinitely long along the backbone, thereby leading to the short relaxation time $\tau$ of the network. It is shown that $\tau$ is proportional to the concentration deviation $\Delta$ near the gelation point. The plateau modulus $G_{\infty}$ increases as the cube of $\Delta$ near the gelation point as a result of the mean-field treatment, and hence the zero-shear viscosity increases as $\eta_0\sim G_{\infty}\tau\sim\Delta^4$. The dynamic shear moduli are well described in terms of the Maxwell model, and it is shown that the present model can explain the concentration dependence of the dynamic moduli for aqueous solutions of telechelic poly(ethylene oxide).