The molecular relaxation mechanisms in the glass transition region and in the liquid crystalline phase exhibited by two side-chain liquid crystalline polysiloxanes have been studied by Thermally Stimulated Discharge Currents. These results were compared with those previously obtained by dielectric r
Molecular motions in a side-chain liquid-crystalline polymethacrylate. A thermally stimulated currents study of the dipolar relaxations in the vitreous and liquid-crystalline phases and at the glass transition
✍ Scribed by João F. Mano; Natália T. Correia; Joaquim J. Moura Ramos; David Coates
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 660 KB
- Volume
- 196
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
In the present work we report the results of a Thermally Stimulated Discharge Currents (TSDC) study of a side‐chain liquid‐crystalline polymer. The different discharges observed in the TSDC spectrum have been analysed by the thermal sampling technique and have been attributed to specific relaxation mechanisms at the molecular level. A particular feature of the polymer studied in this work is that the mesogenic side group presents both longitudinal and transverse components of the dipole moment, and this seems to be at the origin of the presence of two separated relaxations in the liquid‐crystalline phase.
📜 SIMILAR VOLUMES
The relaxation mechanisms present in a side-chain liquid crystalline polymer have been studied by Thermally Stimulated Depolarization Currents (t.s.d.c.), in a wide temperature range covering the glassy state, the glass transition region, and the liquid crystalline phase. The thermal sampling proced
## Abstract Thermal relaxation behavior of a mechanically induced macroscopic orientation of the mesogenic groups in a side‐chain liquid crystalline polyacrylate was investigated using timedependent polarized infrared spectroscopy. It was found that a complete relaxation occurred only at temperatur
## Abstract The synthesis of side‐chain liquid crystalline copolysiloxanes containing ω‐[4‐[4‐[(__S__)‐2‐methylbutoxy]phenoxycarbonyl]‐2‐chlorophenoxy]alkyl side groups is presented. Differential scanning calorimetry, optical polarizing microscopy and X‐ray diffractometry reveal smectic mesomorphis
is highly acknowledged.