Irreversible Shear-Activated Gelation of a Liquid Crystalline Polyelectrolyte

Journal Article (2020)
Author(s)

Ryan J. Fox (University of North Carolina)

Maruti Hegde (University of North Carolina)

Curt J. Zanelotti (Virginia Tech)

Amar S. Kumbhar (University of North Carolina)

Edward T. Samulski (University of North Carolina)

Louis A. Madsen (Virginia Tech)

Stephen J. Picken (TU Delft - ChemE/Advanced Soft Matter)

Theo J. Dingemans (University of North Carolina)

Research Group
ChemE/Advanced Soft Matter
DOI related publication
https://doi.org/10.1021/acsmacrolett.0c00168
More Info
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Publication Year
2020
Language
English
Research Group
ChemE/Advanced Soft Matter
Issue number
7
Volume number
9
Pages (from-to)
957-963

Abstract

We report irreversible, shear-activated gelation in liquid crystalline solutions of a rigid polyelectrolyte that forms rodlike assemblies (rods) in salt-free solution. At rest, the liquid crystalline solutions are kinetically stable against gelation and exhibit low viscosities. Under steady shear at, or above, a critical shear rate, a physically cross-linked, nematic gel network forms due to linear growth and branching of the rods. Above a critical shear rate, the time scale of gelation can be tuned from hours to nearly instantaneously by varying the shear rate and solution concentration. The shear-activated gels are distinct in their structure and rheological properties from thermoreversible gels. At a fixed concentration, the induction time prior to gelation decreases exponentially with the shear rate. This result indicates that shear-activated thermalization of the electrostatically stabilized rods overcomes the energy barrier for rod-rod contact, enabling rod fusion and subsequent irreversible network formation.

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