Four series of copoly(ester-imide)s (co-PEIs) were prepared by transesterification of poly(ethylene terephthalate), PET, with N-(4-carboxyphenyl)trimellitimide and an acetylated diphenol. Methylhydroquinone, tert. butylhydroquinone, phenylhydroquinone, and 2,7-dihydroxynaphthalene were used as diphe
Dielectric relaxation of LC-thermotropic poly(ester imide)s
✍ Scribed by Javier de Abajo; José G. de la Campa; Angel Alegría; José M. Echave
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 253 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0887-6266
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✦ Synopsis
Two different series of poly(ester imide)s, which are distinguished from each other in the orientation of the ester linkages and show well-differentiated thermotropic behavior, are investigated by means of model calculations and dielectric relaxation spectroscopy. Model calculations show that the orientation of the ester linkages has a strong influence on the rotational energy barriers. The dielectric relaxation spectra of both series shows three relaxation regions in the temperature range between 100 and 400 K that have been identified as the a-, band g-relaxation processes. A difference of about two orders of magnitude between the characteristic rates of the g-relaxation is the main feature observed in the dielectric response. However, the b-relaxation shows very similar behavior for both series. The differences in the relaxation behavior in the solid state are interpreted on the basis of the rotational barriers deduced from the model calculation results.
📜 SIMILAR VOLUMES
Two closely series of poly(ester imide)s had been synthesized by solution polycondensation of p-phenylenebis(trimellitate) dianhydride with aliphatic diamines. The differential scanning calorimetry (DSC) traces of the most poly(ester imide)s exhibited two endotherms representing the solid state to a
Several poly(ester imide)s based on 4-N-(carboxyphenyl)trimellitimide, 4-N-(carboxyethenylphenyl)trimellitimide, 4-hydroxy-N-(4-hydroxyphenyl)phthalimide and long aliphatic spacers have been investigated by different solid-state NMR techniques. The conformations of the methylene units were studied b