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Updated: Jul 23, 2025

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer
Published on: November 30, 2020
Reactive phenolic solvents applied to the synthesis of renewable aromatic polyesters with high isosorbide content
Bruno Bottega Pergher1, Narcisa Girigan1, Sietse Vlasblom1
1Van't Hoff Institute of Molecular Sciences, University of Amsterdam P.O. Box 94720 1090GS Amsterdam The Netherlands g.j.m.gruter@uva.nl.
Abstract:
High boiling point phenolic reactive solvents like p-cresol could play a key role in improving the synthesis of aromatic polyesters with a high content of secondary diols such as isosorbide. Previously, our group showed that this method significantly improves the synthesis of poly(isosorbide succinate). In this work, terephthalic acid and 2,5-furandicarboxylic acid were used as building blocks for the synthesis of high Tg polyesters with high isosorbide content (>30 mol% of diols) and high molecular weight (Mn > 24 kg mol-1). A number of reactive and non-reactive solvents were tested in this work, and the results clearly point to a significant improvement when using reactive solvents, in terms of molecular weight and polycondensation time, especially for the case of p-cresol. The synthesis method was successfully scaled to 1 kg, showing promise for production at industrial scale. A method to remove these solvents (including end groups) from the polymers, which uses small excesses of isosorbide (1.5-3.0%) in the feed, is also presented.
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