We present results of analyses of an extensive set of dynamic light scattering (PCS) and viscoelastic (frequency dependent complex moduli) measurements in concentrated aqueous solutions of a triblock copolymer L64 (PEO 13PPO 30PEO 13) micellar system at different temperatures. In particular we study the system dynamical properties in a region of the phase diagram characterized by the existence of a percolation process and a kinetic glass transition. Both the processes, temperature and concentration dependent, are related with adhesive interaction between micelles. The intermediate scattering function (ISF) shows an ergodic to non-ergodic transition on crossing a temperature and concentration dependent line. Viscoelasticity data, determined by means of frequency-dependent complex moduli, satisfy the scaling relations predicted by the scalar elasticity percolation theory and well account for the glass transition process, give indication that percolation and the ergodic non-ergodic transitions take places in separate regions of the phase diagram. Detailed analysis of ISF and rheological data, conducted in terms of the mode coupling theory (MCT) gives evidence of a logarithmic decay on the density fluctuations, which could be attributed to a higher order singularity, followed by a power-law behavior.
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