Synthesis and properties of poly(acrylates-co-urethane) adhesives for low surface energy materials
Source abstract
Abstract
The series of poly(acrylates-co-urethane) were synthesized based on the copolymerization between 2-hydroxyethyl acrylate terminated polyether (or polyester) urethane and acrylate monomers initiated by tri-n-butylborane (TBB). The effects of the soft segment of polyether (or polyester) urethane diacrylate on the copolymer properties were mainly discussed. Polyether (or polyester) urethane was relatively well dispersed in polyacrylate continuous phase, and was intended to aggregate with the increase of soft segment polarity and content. The adhesion to low surface energy materials and loss factor (tan δ) of copolymers were almost not influenced by the soft segment content, but decreased with the increase of soft segment polarity within the scope of the study. On the other hand, the working life of copolymers as adhesives was shortened with the increase of soft segment polarity, but prolonged with the increase of soft segment content. The copolymers with different structures of polyether (or polyester) urethane diacrylate were also shown to be good candidates as adhesives at room temperature.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Advanced Polymer Synthesis and Characterization · Photopolymerization techniques and applications · Epoxy Resin Curing Processes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (38)
Show source-provided references
1. Garbassi · 1994
2. Zhang · Polym Eng Sci · 1998 · 38 · 96510.1002/pen.10264 ↗
3. Drnovska · Colloid Polym Sci · 2003 · 281 · 102510.1007/s00396-003-0871-8 ↗
4. Zhang · Polymer · 1999 · 40 · 29910.1016/S0032-3861(98)00426-1 ↗
5. Mercx · Mater Sci · 1993 · 28 · 75310.1007/BF01151252 ↗
6. Yang · J Appl Polym Sci · 1993 · 48 · 35910.1002/app.1993.070480220 ↗
7. Horst · Prog Org Coat · 2000 · 40 · 4910.1016/S0300-9440(00)00137-5 ↗
8. 1972 · 11 · 692
9. Ghosez · 1989 · E19a · 753
10. Skoultchi MM, Merlo NV. US patent 5,143,884, 1992.
11. Skoultchi MM, Ray-Chaudhuri DK. US patent 5,310,835, 1994.
12. Zharov JV, Krasnov JN. US patent 5,539,070, 1996.
13. Pocius AV, Nigatu TG. US patent 5,616,796, 1997.
14. Pocius AV. US patent 6,093,778,2000.
15. Sonnenschein MF, Webb SP, Rondan N. US patent 2002/0033227, 2002.
16. Sonnenschein MF, Webb SP, Rondan N. US patent 6,730,759, 2004.
17. Kneafsey BJ, Scott EP, Hersee RM. US patent 2006/0122319, 2006.
18. Li · Int J Adhes Adhes · 2011 · 31 · 3610.1016/j.ijadhadh.2010.09.003 ↗
19. Zhang · Macromolecules · 2006 · 39 · 518710.1021/ma061393a ↗
20. Sonnenschein · Macromolecules · 2004 · 37 · 797410.1021/ma040095f ↗
21. Sonnenschein · Macromolecules · 2006 · 39 · 250710.1021/ma060268w ↗
22. Hirokazu · J Polym Sci Part A: Polym Chem · 2009 · 47 · 616310.1002/pola.23659 ↗
23. Pocius AV. CN patent 1,259,554, 2000.
24. Molen DM. CN patent 1,418,246, 2003.
25. Sonnenschein MF, Webb SP, Wendt B, Harrington DR. WO patent 03/076485, 2003.
26. Sonnenschein · J Polym Sci Part A: Polym Chem · 2007 · 45 · 98910.1002/pola.21843 ↗
27. Sonnenschein · Int J Adhes Adhes · 2008 · 28 · 12610.1016/j.ijadhadh.2007.07.001 ↗
28. Deviny EJ. US patent 5,872,197, 1999.
29. Deviny EJ. US patent 5,990,036, 1999.
30. Pocius AV. US patent 5,686,544, 1997.
31. Pocius AV. US patent 6,008,308, 1999.
32. Hirose · Prog Org Coat · 2000 · 38 · 2710.1016/S0300-9440(99)00081-8 ↗
33. Kukanja · J Appl Polym Sci · 2002 · 84 · 263910.1002/app.10440 ↗
34. Chai · Eur Polym J · 2008 · 44 · 330610.1016/j.eurpolymj.2008.07.038 ↗
35. Kukanja · J Appl Polym Sci · 2000 · 78 · 6710.1002/1097-4628(20001003)78:1<67::AID-APP100>3.0.CO;2-4 ↗
36. Wu · J Appl Polym Sci · 2002 · 84 · 162010.1002/app.10526 ↗
37. Li · J Appl Polym Sci · 2010 · 118 · 320310.1002/app.32761 ↗
38. Brown · J Org Chem · 1986 · 51 · 42710.1021/jo00354a002 ↗