Blends of poly(ethylene terephthalate) with Co[poly(ethylene terephthalate-p-oxybenzoate)]. IV. Interchange reactions and their effects on the thermal and crystallization behaviors
β Scribed by Cheng-Fang Ou; Chen-Chong Lin
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 550 KB
- Volume
- 61
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
Poly(ethy1ene terephthalate) (PET) was blended with a co[poly(ethylene terephthalatep-oxybenzoate)] (POB-PET) copolyester which is a liquid crystalline polymer consisting ofp-oxybenzoate and ethylene terephthalate units in a 40/60 mol ratio (P46). The level of P46 liquid crystalline polymer varies from 10 to 50 wt %. All the blends were prepared by melt-mixing in a Brabender Plasticorder at 275'C for different times. The thermal and crystallization behaviors of blends depend on the blending time and the composition of blends, viz., the content of the p-oxybenzoate (POB) moiety incorporated into the blends.
The interchange reactions detected by proton NMR analysis occur during the processing at a greater level if the blending time increases. These interchange reactions hinder the crystallization processes of PET and result in a decrease of the melting point, the heat of fusion, crystallization temperature, and the heat of crystallization of the original PET. The effects of the interchange reaction on thermal and crystallization behaviors of the blends may be attributed to the insertion of the rigid POB units into the soft P E T chain.
π SIMILAR VOLUMES
## Abstract Poly(ethylene terephthalate) (PET) was blended with two different poly(oxybenzoateβ__p__βtrimethylene terephthalate) copolymers, designated T28 and T64, with the level of copolymer varying from 1 to 15 wt %. All samples were prepared by solution blending in a 60/40 (by weight) phenol/te
Poly(ethylene terephthalate) (PET) was blended with three different kinds of co[poly(butylene terephthalate-p-oxybenzoate)] copolyesters, designated B28, B46, and B64, with the level of copolyester varying from 1 to 15 wt %. All samples were prepared by solution blending in a 60/40 by weight phenol/