The search for rigid, tough polyesters with high Tg - renewable aromatic polyesters with high isosorbide content
| Authors | |
|---|---|
| Publication date | 01-09-2024 |
| Journal | RSC Sustainability |
| Volume | Issue number | 2 | 9 |
| Pages (from-to) | 2644-2656 |
| Number of pages | 13 |
| Organisations |
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| Abstract |
Renewable polyesters with a good balance between impact strength and
elastic modulus (stiffness) are not very common, especially when
combined with high glass transition temperature (Tg).
Achieving such high performance properties would enable the
substitution of high performance polymers like ABS and polycarbonate
with chemically recyclable polyesters from bio-based or recycled
sources. One of the challenges in developing these materials is to
select the right composition of the right monomers/comonomer ratios and
making these materials with high molecular weight, which can be
challenging since some of the most promising rigid diols, such as
isosorbide, are unreactive. This study comprises aromatic polyesters
from (potentially) renewable monomers, using bio-based isosorbide as a
means to increase their Tg and to
inhibit their crystallization, while using flexible co-diols to improve
impact strength. To incorporate a high amount of isosorbide into the
targeted polyesters, we used the synthesis method with reactive phenolic
solvents previously developed in our group. The selected compositions
display high Tg's (>90 °C) and
high tensile modulus (>1850 MPa). We show that more polar monomers
such as the stiffer 2,5-furandicarboxylic acid (FDCA) and diethylene
glycol cause high stiffness but decreased impact strength (<5 kJ m−2).
Combining terephthalic acid and isosorbide with more flexible diols
like 1,4-butanediol, 1,4-cyclohexanedimethanol (CHDM) and
1,3-propanediol provides a better balance, including the combination of
high tensile modulus (>1850 MPa) and high impact strength (>10 kJ m−2).
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| Document type | Article |
| Note | With supplementary file. |
| Language | English |
| Published at | https://doi.org/10.1039/d4su00294f |
| Published at | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85200671592&doi=10.1039%2fd4su00294f&partnerID=40&md5=bfbc07122ca36fdf312b678f94439762 |
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