Paper Number
PG17 

Session
Polyelectrolytes, Self-assembling Systems & Gels

Title
Dynamics of liquid coacervates formed by oppositely charge polyelectrolytes

Presentation Date and Time
October 17, 2018 (Wednesday) 2:45

Track / Room
Track 3 / Bellaire

Authors (Click on name to view author profile)

1. Aponte-Rivera, Christian (Duke University, Mechanical Engineering and Material Science)
2. Rubinstein, Michael (Duke University, Mechanical Engineering and Materials Science)

Author and Affiliation Lines (in printed abstract book)
Christian Aponte-Rivera and Michael Rubinstein
Mechanical Engineering and Materials Science, Duke University, Durham, NC 27710

Speaker / Presenter 
Aponte-Rivera, Christian

Text of Abstract
Mixtures of oppositely charged polyelectrolytes can undergo phase separation to form a polymer rich phase called a coacervate and a polymer depleted phase. The polymer rich phase can be a soft, viscous liquid, or a solid like complex. Both types have drawn much attention in the literature due to their applications in the food, pharmaceutical, and other industries as well as their role in biological systems. Studies have focused on the formation of the coacervate phase, and models have been developed to predict phase separation and static properties. However, much less attention has been given to predicting the dynamic properties of coacervates, and how these depend on experimentally controllable parameters. We develop a scaling theory for the dynamic behavior of asymmetric liquid-like coacervates formed from oppositely charged polyelectrolyte solutions. Depending on the degree of polymerization, the asymmetric liquid coacervate can form either an interpenetrating double-semidilute structure, wherein both polyanion and polycation are found above their overlap concentration, or a dilute-semidilute structure, where only lower charged polyelectrolytes are found above their overlap concentration. We will discuss a scaling theory for the entangled and unentangled dynamics, providing predictions for the relaxation modulus and steady state shear viscosity of the coacervate, and the diffusivity of the polyelectrolyte chains. The scaling theory will highlight the different dynamical regimes of the system, and how the dynamic properties can be tuned from experimentally controllable parameters such as the degree of polymerization, the number density of charges of the polyanion and polycation, and the strength of electrostatic interactions. The scaling theory provides guidelines for optimizing the dynamic and rheological properties for future applications in the cosmetics, food, and other industries.