Most, but not all, liquid crystals tend to align when subject to shear flow, while most nematic polymeric liquid crystals undergo a tumbling instability, where the director rotates with the flow. The reasons of this instability remain elusive, as it is possible to find similar molecules exhibiting opposite behaviors. We propose a continuum theory suitable for describing a wide range of material behaviors, ranging form nematic elastomers to nematic polymers and nematic liquid crystals, where the material parameters have meaningful physical interpretations and the conditions for tumbling emerge clearly. There are two possible ways to relax the internal stress in a nematic material. The first is the reorganization of the polymer network, the second is the alignment of the network natural axis with respect to the principal direction of the effective strain. We show that tumbling occurs whenever the second mechanism is less efficient than the first. Furthermore, we provide a justification of the experimental fact that at high temperatures, in an isotropic phase, only flow alignment is observed and no tumbling is possible, even in polymers.

Two-shape-tensor model for tumbling in nematic polymers and liquid crystals

Turzi S. S.
2019-01-01

Abstract

Most, but not all, liquid crystals tend to align when subject to shear flow, while most nematic polymeric liquid crystals undergo a tumbling instability, where the director rotates with the flow. The reasons of this instability remain elusive, as it is possible to find similar molecules exhibiting opposite behaviors. We propose a continuum theory suitable for describing a wide range of material behaviors, ranging form nematic elastomers to nematic polymers and nematic liquid crystals, where the material parameters have meaningful physical interpretations and the conditions for tumbling emerge clearly. There are two possible ways to relax the internal stress in a nematic material. The first is the reorganization of the polymer network, the second is the alignment of the network natural axis with respect to the principal direction of the effective strain. We show that tumbling occurs whenever the second mechanism is less efficient than the first. Furthermore, we provide a justification of the experimental fact that at high temperatures, in an isotropic phase, only flow alignment is observed and no tumbling is possible, even in polymers.
2019
File in questo prodotto:
File Dimensione Formato  
PhysRevE.100.012706.pdf

accesso aperto

Descrizione: Versione pubblicata
: Publisher’s version
Dimensione 349.48 kB
Formato Adobe PDF
349.48 kB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11311/1105870
Citazioni
  • ???jsp.display-item.citation.pmc??? 0
  • Scopus 2
  • ???jsp.display-item.citation.isi??? 2
social impact