Please use this identifier to cite or link to this item:
https://doi.org/10.1021/ma010895f
Title: | Phase transition and transition kinetics of a thermotropic poly(amide-imide) derived from 70% pyromellitic dianhydride, 30% terephthaloyl chloride, and 1,3-bis[4-(4′-aminophenoxy)cumyl]benzene | Authors: | Liu, S.L. Chung, T.S. Geng, J.X. Zhou, E.L. Tamai, S. |
Issue Date: | 4-Dec-2001 | Citation: | Liu, S.L., Chung, T.S., Geng, J.X., Zhou, E.L., Tamai, S. (2001-12-04). Phase transition and transition kinetics of a thermotropic poly(amide-imide) derived from 70% pyromellitic dianhydride, 30% terephthaloyl chloride, and 1,3-bis[4-(4′-aminophenoxy)cumyl]benzene. Macromolecules 34 (25) : 8710-8719. ScholarBank@NUS Repository. https://doi.org/10.1021/ma010895f | Abstract: | The phase transition and transition kinetics of a liquid crystalline copoly(amide-imide) (PA137), which was synthesized from 70 mol % pyromellitic dianhydride, 30 mol % terephthaloyl chloride, and 1,3-bis[4-(4′-aminophenoxy)cumyl]benzene, was characterized by differential scanning calorimetry, polarized light microscopy, X-ray diffraction, and rheology. PAI37 exhibits a glass transition temperature at 182°C followed by multiple phase transitions. The crystalline phase starts to melt at ∼220°C and forms smectic C (SC) phase. The SC phase transforms into smectic A (SA) phase when the temperature is above 237°C. The SC to SA transition spans a broad temperature range in which the SA phase vanishes and forms isotropic melt. The WAXD fiber pattern of PAI37 pulled from the anisotropic melt revealed an direction. The transition kinetics for the mesophase and crystalline phase formation was also studied. | Source Title: | Macromolecules | URI: | http://scholarbank.nus.edu.sg/handle/10635/92227 | ISSN: | 00249297 | DOI: | 10.1021/ma010895f |
Appears in Collections: | Staff Publications |
Show full item record
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.