Full Paper
Copolyesters of Lactide, Isosorbide, and Terephthalic Acid-Biobased, Biodegradable, High-Tg Engineering Plastics
Article first published online: 4 FEB 2013
DOI: 10.1002/macp.201200612
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Kricheldorf, H. R. and Weidner, S. M. (2013), Copolyesters of Lactide, Isosorbide, and Terephthalic Acid-Biobased, Biodegradable, High-Tg Engineering Plastics. Macromol. Chem. Phys., 214: 726–733. doi: 10.1002/macp.201200612
Publication History
- Issue published online: 13 MAR 2013
- Article first published online: 4 FEB 2013
- Manuscript Revised: 26 NOV 2012
- Manuscript Received: 22 OCT 2012
- Abstract
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Keywords:
- biodegradability;
- cyclization;
- isosorbide;
- polycondensation;
- ring-opening polymerization
Abstract
Various copolyesters of lactide, isosorbide, and terephthalic acid are prepared by a two-step process performed in a “one-pot” procedure, beginning with an isosorbide-initiated oligomerization of L-lactide followed by polycondensation with terephthaloyl chloride using SnCl2 as a catalyst for both steps. The SEC data show the formation of random copolyesters with high polydispersities as a consequence of the relatively high fraction of cyclics proved by matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS). The glass-transition temperatures (89–180 °C) obey an almost linear trend with the molar composition. The thermostability decreases with increasing lactide content. The successful incorporation of phenyl phosphate results in copolyesters of lower inflammability.

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