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 (T g). 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 T g 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 T g'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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