Journal
PROGRESS IN ORGANIC COATINGS
Volume 86, Issue -, Pages 134-142Publisher
ELSEVIER SCIENCE SA
DOI: 10.1016/j.porgcoat.2015.04.018
Keywords
Renewable; Water-borne polyurethanes; Isosorbide; Dimer biobased diisocyanate; Isosorbide; Chain extension
Funding
- Dutch Polymer Institute [658]
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Poly(urethane urea)s dispersed in water were prepared from biobased monomers, including a fatty acid-derived diisocyanate (DDI), the lysine-derived ethyl ester L-lysine diisocyanate (EELDI) and 1,4:3,6-dianhydro-D-glucitol (isosorbide, IS). Ionic stabilization of the polymer particles in water was achieved by incorporating dimethylolpropionic acid (DMPA) in the polyurethane backbone. The synthesis of isocyanate-functional prepolymers with number-average molecular weights (Ma) of approximately 6000 g/mol was followed by their dispersion in water and chain extension using ethylene diamine. The chain extension procedure was optimized, resulting in final Mn values of approximately 17,000 g/mol. The replacement of DO! by EELDI and the incorporation of IS into the polymer composition effectively reduced the required amount of DMPA from 6.0 to 2.0 wt% to render stable dispersions and significantly enhanced the T-g values of dispersion-cast films to 60 degrees C (1st T-g) and to above 70 degrees C (2nd T-g), however, at the expense of slightly reduced thermal stability. The asymmetric structure of EELDI and its pendant ester group potentially facilitated the dispersion stability, the latter through possible (partial) hydrolysis. Accordingly, aqueous PU dispersions with a renewable content up to 97 wt% and sufficiently high, tunable film T-g values have been obtained. (C) 2015 Elsevier B.V. All rights reserved.
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