The influence of the molecular structure of homogeneous fluids comprised of liquid crystalline polysiloxanes (LCSs) diluted in polydimethylsiloxane (DMS), on the increase in their viscosity upon application of an electric field (electrorheological effect, or the ER effect) was investigated, particul
Electrorheological effect of liquid crystalline polymers
β Scribed by A. Inoue; S. Maniwa
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 415 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
β¦ Synopsis
Large increases in shear stress upon application of a 2.0 kV/mm electric field were observed in homogeneous fluids composed of polysiloxane-based liquid crystalline polymers (LCPs) in dimethyl silicone at a shear rate of 200 s-*. The increase was largest (about 3,000 Pa at 50Β°C) with LCP consisting of a polysiloxane bearing mesogenic groups as side chains. With LCP having the mesogenic groups within the main chain, the maximum increase was about 1,300 Pa at 90Β°C. It was about 400 Pa at 30Β°C with LCP having the mesogenic groups at both ends only (biterminal), and several Pa a t 30Β°C with LCP having the mesogenic group at one end only (monoterminal). The increases were smaller with mesogenic groups of lower positive dielectric anisotropy in the side chain LCP. The side chain, biterminal, and monoterminal LCPs exhibited Newtonian flow in the electric field and shear stress yield at low shear rates in its absence. The complex dynamic modulus and viscosity of the side chain LCP in the electric field showed no dependence on strain at deformation displacements approaching 5", but in its absence were generally strain-dependent, and suggest the strong electrorheological effect of these homogeneous LCP fluids is related to a flexible-chain linkage between their crystalline domains. 0 1995 John Wiley & Sons, Inc.
π SIMILAR VOLUMES
A thermotropic liquid crystalline (LC) polymer, consisting of an LC silicone having benzoic acid phenylester LC groups as side chains of the siloxane polymer main chain diluted with dimethylsilicone, and a lyotropic LC polymer solution, consisting of poly(y-benzyl-L-glutamate) in 1,4-dioxane, both s
The rheological characterization of two commercial thermotropic liquid crystalline polymers based on poly(ethylene terephthalate) (PET) and para-hydroxybenzoic acid (PHB) is carried out. The thermal transitions determined by DMTA are explained by the random character of these copolyesters, in compar
A liquid crystalline polysiloxane (LCP), having an ether bond in the spacer between its siloxane main chain and its mesogenic-group side chains, exhibited a very small electrorheological (ER) effect or increase in shear stress upon application of an electric field, but mixtures of the LCP and polydi
News could, in principle, be polaron formation. However, the absence of a noticeable temperature dependence argues against this notion. Comparison with the p(T) behavior of polymeric systems above T, suggests instead a common underlying principle. It is known that molecular motion is turned on upon