People | Locations | Statistics |
---|---|---|
Naji, M. |
| |
Motta, Antonella |
| |
Aletan, Dirar |
| |
Mohamed, Tarek |
| |
Ertürk, Emre |
| |
Taccardi, Nicola |
| |
Kononenko, Denys |
| |
Petrov, R. H. | Madrid |
|
Alshaaer, Mazen | Brussels |
|
Bih, L. |
| |
Casati, R. |
| |
Muller, Hermance |
| |
Kočí, Jan | Prague |
|
Šuljagić, Marija |
| |
Kalteremidou, Kalliopi-Artemi | Brussels |
|
Azam, Siraj |
| |
Ospanova, Alyiya |
| |
Blanpain, Bart |
| |
Ali, M. A. |
| |
Popa, V. |
| |
Rančić, M. |
| |
Ollier, Nadège |
| |
Azevedo, Nuno Monteiro |
| |
Landes, Michael |
| |
Rignanese, Gian-Marco |
|
Martello, Mark T.
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (5/5 displayed)
- 2015Poly(lactide)-block-poly(ε-caprolactone-co-ε-decalactone)-block-poly(lactide) copolymer elastomerscitations
- 2014Synthesis and melt processing of sustainable poly(ε-decalactone)-block-poly(lactide) multiblock thermoplastic elastomerscitations
- 2012Bulk ring-opening transesterification polymerization of the renewable δ-decalactone using an organocatalystcitations
- 2011Functional biorenewable polyesters from carvone-derived lactonescitations
- 2011Pressure-sensitive adhesives from renewable triblock copolymerscitations
Places of action
Organizations | Location | People |
---|
article
Synthesis and melt processing of sustainable poly(ε-decalactone)-block-poly(lactide) multiblock thermoplastic elastomers
Abstract
<p>A one-pot, one-catalyst, sequential ring-opening transesterification polymerization (ROTEP) was used to prepare fully renewable amorphous poly(d,l-lactide)-poly(ε-decalactone)-poly(d,l-lactide) (LDL) triblock polymers. These α,ω hydroxy-telechelic polymers were subsequently coupled to prepare linear alternating (LDL)<sub>n</sub> multiblock polymers. Differential scanning calorimetry (DSC) and small-angle X-ray scattering (SAXS) indicated microphase separation into two domains in both the triblock and multiblock architectures. The temperature dependent Flory-Huggins interaction parameter for this system, X(T) = 69.1/T - 0.072, was estimated from the experimentally determined order-disorder transition temperature (T<sub>ODT</sub>) values of four symmetric LDL triblock polymers. Uniaxial extension tests revealed a dramatic dependence of the room-temperature mechanical properties on overall molar mass. Additionally, coupling low molar mass LDL triblocks to prepare (LDL)<sub>n</sub> multiblocks led to substantial increases in the ultimate elongation and tensile stress at break. Compared to high molar mass triblocks with inaccessible T<sub>ODT</sub> values, (LDL)<sub>n</sub> multiblocks of similar composition and molar mass were found to disorder at much lower temperatures (T<sub>ODT</sub> < 150 °C). Because of this, it was possible to process (LDL)<sub>n</sub> using injection molding. The simple synthetic procedure and melt processability of the (LDL)<sub>n</sub> multiblock polymers make these multiblocks attractive as renewable thermoplastic elastomers (TPEs).</p>