journal article·2016-01-02

Synthesis and properties of photopolymerizable bifunctional polyether-modified polysiloxane polyurethane acrylate prepolymer

Jiye Cheng, Minglei Li, Yue Cao, Yanjing Gao, Jiancheng Liu, Fang Sun

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Abstract

A UV-curable polyether-modified polysiloxane polyurethane acrylate prepolymer PESiUA that can be used for polyvinyl chloride leather finishing agents has been synthesized and characterized by nuclear magnetic resonance, Fourier transform infrared spectroscopy, and gel permeation chromatography. The prepolymer exhibited excellent compatibility with acrylate monomers, satisfying photopolymerization efficiency and good yellowing resistance. The influences of the monomers on the properties of the UV-cured film were systematically studied. The results showed that the increase in the functionality of monomers can increase the thermostability, glass transition temperature, tensile strength, tensile modulus, dispersion surface energy, and decrease the contact angle and elongation at break. More significantly, the PVC leather finishing agent designed based on the photopolymerizable polyether-modified polysiloxane polyurethane acrylate prepolymer PESiUA possessed excellent performances and had great application potential, due to the combination of advantages of polysiloxane segment and polypropylene glycol segment as well as photopolymerization technique.
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Research context

OpenAlex topics: Photopolymerization techniques and applications · Silicone and Siloxane Chemistry · Polymer composites and self-healing

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (22)

Show source-provided references
1. 10.1002/(ISSN)1099-051810.1002/(ISSN)1099-0518 ↗
2. 10.1016/j.progpolymsci.2010.01.00710.1016/j.progpolymsci.2010.01.007 ↗
3. 10.1016/j.progpolymsci.2013.11.00310.1016/j.progpolymsci.2013.11.003 ↗
4. 10.1016/j.matdes.2012.10.01610.1016/j.matdes.2012.10.016 ↗
5. 10.1016/j.jfluchem.2013.11.01510.1016/j.jfluchem.2013.11.015 ↗
6. 10.1021/ie071443f10.1021/ie071443f ↗
7. 10.1016/j.porgcoat.2005.01.00610.1016/j.porgcoat.2005.01.006 ↗
8. 10.1016/j.porgcoat.2009.09.00510.1016/j.porgcoat.2009.09.005 ↗
9. 10.1016/j.porgcoat.2013.01.00710.1016/j.porgcoat.2013.01.007 ↗
10. 10.14233/ajchem10.14233/ajchem ↗
11. 10.1016/j.polymer.2010.04.03810.1016/j.polymer.2010.04.038 ↗
12. 10.1016/j.jsps.2013.01.00510.1016/j.jsps.2013.01.005 ↗
13. 10.1016/j.polymer.2010.04.03810.1016/j.polymer.2010.04.038 ↗
14. 10.1016/j.ijpharm.2004.05.03010.1016/j.ijpharm.2004.05.030 ↗
15. 10.1021/bm700543c10.1021/bm700543c ↗
16. Sun F · Chin. J. Anal. Lab · 2007 · 26 · 73
17. 10.1016/j.jphotochem.2007.03.02710.1016/j.jphotochem.2007.03.027 ↗
18. 10.1007/s10965-010-9491-410.1007/s10965-010-9491-4 ↗
19. 10.1002/(ISSN)1097-462810.1002/(ISSN)1097-4628 ↗
20. 10.1016/j.matdes.2012.06.00810.1016/j.matdes.2012.06.008 ↗
21. 10.1016/j.tca.2014.08.01810.1016/j.tca.2014.08.018 ↗
22. 10.1016/j.tca.2013.04.02710.1016/j.tca.2013.04.027 ↗