The degradation of poly(oxyethylene) -poly( 1-caprolactone) (POE-PCL) multiblock copolymers was investigated at 37ЊC in a 0.13M, pH 7.4 phosphate buffer selected to mimic in vivo conditions. The copolymers were obtained by coupling polycaprolactone diols and poly(ethylene glycol) diacids using dicyc
Study of poly-ϵ-caprolactone bulk degradation
✍ Scribed by T. Ouhadi; C. Stevens; Ph. Teyssié
- Publisher
- John Wiley and Sons
- Year
- 1976
- Tongue
- English
- Weight
- 450 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0021-8995
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✦ Synopsis
The thermal stability of poly-c-caprolactone samples obtained by ring-opening polymerization in the presence of different metal alkoxides has been investigated. A significant degradation of the polyesters is observed under isothermal conditions at 120OC. The degradation is related to the nature of the endgroup, the presence of catalyst residues, and the presence of molecular oxygen. The hydroxyl endgroups play a determinant role in the process. They probably give rise, under the influence of catalyst residues, to hydroperoxides which are responsible for the polymer degradation by a radical reaction. It is shown that this is clearly different from the change in molecular weights distribution due to the well-known ester interchange reaction (transesterification equilibrium). Resulting methods for the polymers stabilization are indicated.
📜 SIMILAR VOLUMES
## Abstract The thermal degradation of ternary blends of poly(ε‐caprolactone) (PCL), poly(vinyl acetate) (PVAC), and poly(vinyl chloride) (PVC) was studied using a thermogravimetry analyzer under dynamic heating in flowing nitrogen atmosphere. PCL degraded in a single stage, whereas the PVAC and PV