Newly UV-Curable Polyurethane Coatings Prepared by Multifunctional Thiol- and Ene-Terminated Polyurethane Aqueous Dispersions: Photopolymerization Properties
Document Type
Article
Publication Date
3-24-2010
Department
Polymers and High Performance Materials
Abstract
A novel approach toward the preparation of newly UV-curable polyurethane coatings composed of multifunctional thiol- and ene-terminated polyurethane aqueous dispersions is presented. By a synergistic combination of polyurethane dispersions synthesis and thiol-ene chemistry, strategies for the preparation of newly UV-curable polyurethane coatings are developed. Photo-DSC, real-time FTIR, DMA and tensile tests measurements are used to investigate the photopolymerization and mechanical behaviors of newly UV-curable polyurethane coatings. The newly polyurethane coatings have 1.5 times higher polymerization rate and final 99% functional groups conversion in air conditions compared to current urethane-acrylate based UV-curable polyurethane dispersions coatings. UV-cured polyurethane films prepared by this method are also found to exhibit increase in Young's modulus and tensile strength at break by 25% and 10%, respectively. These experiment facts suggest that the incorporation of thiol-ene chemistry to the polyurethane dispersion coatings increase their polymerization rate, producing a high degree of cross-linking. This confirms the preparation of the targeted novel UV-curable polyurethane coatings and reveals the dramatic effect that changes in incorporation of thiol-ene chemistry can have on the photopolymerization behaviors of UV-curable polyurethane dispersions coatings systems. Crown Copyright (C) 2010 Published by Elsevier Ltd. All rights reserved.
Publication Title
Polymer
Volume
51
Issue
7
First Page
1572
Last Page
1577
Recommended Citation
Yang, Z.,
Wicks, D. A.,
Yuan, J.,
Pu, H.,
Liu, Y.
(2010). Newly UV-Curable Polyurethane Coatings Prepared by Multifunctional Thiol- and Ene-Terminated Polyurethane Aqueous Dispersions: Photopolymerization Properties. Polymer, 51(7), 1572-1577.
Available at: https://aquila.usm.edu/fac_pubs/994