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arXiv · 2410.15132

Tuning the shear and extensional rheology of semi-flexible polyelectrolyte solutions

H. Moon·S. Yamani·G. H. McKinley·J. Lee
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Abstract

Semi-flexible polyelectrolytes are a group of biopolymers with a wide range of applications from drag reducing agents in turbulent flows to thickening agents in food and cosmetics. In this study, we investigate the rheology of aqueous solutions of xanthan gum as a canonical semi-flexible polyelectrolyte in steady shear and transient extensional flows via torsional rheometry and dripping-onto-substrate (DoS), respectively. The high molecular weight of the xanthan gum and the numerous charged groups on the side branches attached to the backbone allow the shear and extensional rheology of the xanthan gum solutions to be tuned over a wide range by changing the ionic strength of the solvent. In steady shear flow, increasing the xanthan gum concentration increases both the zero shear viscosity and the extent of shear-thinning of the solution. Conversely, increasing the ionic strength of the solvent by addition of sodium chloride (NaCl) decreases both the zero shear viscosity and the level of shear-thinning. In transient extensional flow, increasing the xanthan gum concentration changes the dynamics of the capillary thinning from an inelastic power-law (IP) response to an elastocapillary (EC) balance, from which an extensional relaxation time can be measured based on the rate of filament thinning. Increasing the NaCl concentration decreases the extensional relaxation time and the transient extensional viscosity of the viscoelastic solution. Based on the dynamics of capillary thinning observed in the DoS experiments, we provide a relationship for the smallest extensional relaxation time that can be measured using DoS. We suggest that the change in the dynamics of capillary thinning from an IP response to an EC response can be used as an easy and robust experimental method for identifying the rheologically effective overlap concentration of a semi-flexible polyelectrolyte solution, i.e., the critical concentration at which polymer molecules start to interact with each other to produce a viscoelastic strain-stiffening response (often perceived as "stringiness") in transient extensional flows such as those involved in dripping, dispensing and filling operations.

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H. Moon, S. Yamani, G. H. McKinley, J. Lee. 2024-10-19. Tuning the shear and extensional rheology of semi-flexible polyelectrolyte solutions. https://arxiv.org/abs/2410.15132

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