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Observation of transition cascades in sheared liquid crystalline polymers.

作者信息

Fox Ryan J, Forest M Gregory, Picken Stephen J, Dingemans Theo J

机构信息

Department of Applied Physical Sciences, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-3050, USA.

Faculty of Applied Sciences, Delft University of Technology, Van der Maasweg 9, 2629 HZ Delft, The Netherlands.

出版信息

Soft Matter. 2020 Apr 29;16(16):3891-3901. doi: 10.1039/d0sm00275e.

DOI:10.1039/d0sm00275e
PMID:32242188
Abstract

We report on the shear rheology of liquid crystalline solutions composed of charged, rodlike polymers that form supramolecular assemblies dispersed in water. Under steady shear, we observe shear thickening behavior, followed by a hesitation in the viscosity accompanied by an extremely narrow range of negative first normal stress difference. The Peclet number (Pe, shear rate normalized by rod rotational diffusivity) for the onset of shear thickening is in agreement with previous, high-resolution numerical simulations of the Doi-Edwards-Hess kinetic theory. We interrogate these dynamic responses through shear step-down experiments, revealing a complex evolution of transient responses. Detailed analysis of the stress transients provides compelling evidence that the principal axis of the rod orientational distribution, the nematic director, undergoes a cascade of transitions and coexistence of periodic states known as kayaking, tumbling, and wagging, before transitioning to steady flow alignment above a critical shear rate.

摘要

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