## Abstract EVOH‐__g__‐PCL were prepared by a solvent‐free reactive extrusion process using a co‐rotating twin screw extruder. Kinetic simulations were made of selected reaction conditions at 185 °C. Changes in the screw rotation rate resulted in evolution of the residence time distribution and sli
Poly[ethylene-co-(vinyl alcohol)]-graft-poly(ε-caprolactone) Synthesis by Reactive Extrusion, 1 - Structural and Kinetic Study
✍ Scribed by Frédéric Becquart; Yvan Chalamet; Jianding Chen; Yanchao Zhao; Mohamed Taha
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 322 KB
- Volume
- 294
- Category
- Article
- ISSN
- 1438-7492
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Chemical modification of EVOH in the molten state at 185 °C by a grafting from process of poly(ε‐caprolactone) in batch was studied. ^1^H NMR was used to characterize the structure evolutions of PCL grafts. In addition to grafting reactions, dynamic covalent transesterification reactions between EVOH residual alcohols and the polyester grafts led to a redistribution of the PCL grafts length. $\mathop {\overline {Dp} }\nolimits_n $ up to 27 and SR up to 80% were obtained. Experiments made in a corotating mini twin‐screw extruder also confirmed these results. The effect of the alcohol to caprolactone ratio and catalyst concentration (SnOct~2~) on kinetic evolution showed that few minutes were necessary to complete the polymerization. A kinetic model was proposed and adequate conditions for the synthesis by reactive extrusion were defined.
magnified image
📜 SIMILAR VOLUMES
## Abstract **Summary:** The objective of this study was to synthesize thermoplastic elastomers by the direct copolyesterification of reactive oligomers of poly[(ethylene terephthalate)‐__co__‐(__ε__‐caprolactone)] (PET) and poly(propylene oxide) (PPO). The synthesis of hard segment oligomers was a