Preparation and characterization of polarity-modulated SIS-based hot-melt pressure-sensitive adhesives
Source abstract
Abstract
In order to develop polarity-modulated hot-melt pressure-sensitive adhesives (HMPSAs), epoxidation of styrene-isoprene-styrene (SIS) copolymers, using in situ prepared per-formic acid was studied. The polymers were characterized with Fourier-transform infrared spectroscopy, 1H nuclear magnetic resonance spectroscopy, differential scanning calorimetry, and contact angle tests. The epoxidation degree linearly increases with the epoxidation time without side reaction at low temperature. The polarity of the polymers increases with the epoxidation degree. At low epoxidation degree, the 180° peel strength of epoxidated-SIS-based HMPSA increases with the epoxidation degree. In epoxidated-SIS-based HMPSAs, ESIS plays the role of compatibilizer.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Polymer Synthesis and Characterization · Synthesis and properties of polymers · Epoxy Resin Curing Processes
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (40)
Show source-provided references
1. Silva SA · J. Adhes · 2012 · 88 · 18710.1080/00218464.2012.648873 ↗
2. Yan XP · Chin. J. Chin. Materia Med · 2009 · 34 · 1612
3. 10.1002/app.2324110.1002/app.23241 ↗
4. Wu CY · J. Appl. Polym. Sci · 2006 · 102 · 415710.1002/app.24447 ↗
5. 10.1080/0021846059095461010.1080/00218460590954610 ↗
6. 10.1080/0021846049088425910.1080/00218460490884259 ↗
7. 10.1080/0021846030955210.1080/00218460309552 ↗
8. 10.1002/app.1130010.1002/app.11300 ↗
9. 10.1016/S0032-3861(99)00585-610.1016/S0032-3861(99)00585-6 ↗
10. 10.1002/(SICI)1097-4628(19961121)62:8<1263::AID-APP17>3.0.CO;2-810.1002/(SICI)1097-4628(19961121)62:8<1263::AID-APP17>3.0.CO;2-8 ↗
11. Benedek I · 200810.1201/9781420059410 ↗
12. 10.1208/s12249-012-9778-310.1208/s12249-012-9778-3 ↗
13. 10.1016/j.ijadhadh.2011.12.00210.1016/j.ijadhadh.2011.12.002 ↗
14. Yu ZW · Chin. J. Chin. Materia Med · 2011 · 36 · 2967
15. 10.1163/15685610778119232810.1163/156856107781192328 ↗
16. 10.1163/15685610677845661810.1163/156856106778456618 ↗
17. 10.1002/app.2457110.1002/app.24571 ↗
18. 10.1163/15685610577480585910.1163/156856105774805859 ↗
19. 10.1016/j.ijadhadh.2004.10.00110.1016/j.ijadhadh.2004.10.001 ↗
20. 10.1163/156856104270841210.1163/1568561042708412 ↗
21. Wilhelm HM · J. Appl. Polym. Sci · 2002 · 83 · 295310.1002/app.10355 ↗
22. Ramos JA · Macromolecules · 2012 · 45 · 148310.1021/ma2018759 ↗
23. Garate H · J. Polym. Sci., Part A: Polym. Chem · 2011 · 49 · 450510.1002/pola.24893 ↗
24. 10.1016/j.msec.2010.06.01410.1016/j.msec.2010.06.014 ↗
25. Barreto SMA · J. Membr. Sci · 2010 · 362 · 47110.1016/j.memsci.2010.06.061 ↗
26. Li HQ · J. Elastomers Plast · 2008 · 40 · 31710.1177/0095244307086713 ↗
27. Choi S · Macromolecules · 2003 · 36 · 622010.1021/ma030253n ↗
28. 10.1002/macp.20030012310.1002/macp.200300123 ↗
29. 10.1021/ma951446g10.1021/ma951446g ↗
30. Grubbs RB · Macromolecules · 2000 · 33 · 230810.1021/ma992049z ↗
31. Ocando C · Polym. Int · 2008 · 57 · 133310.1002/pi.2478 ↗
32. Serrano E · Macromol. Chem. Phys · 2007 · 208 · 228110.1002/macp.200700169 ↗
33. Zhang Y · J. Appl. Polym. Sci · 2001 · 81 · 298710.1002/app.1748 ↗
34. 10.1002/pola.1991.08029081210.1002/pola.1991.080290812 ↗
35. 10.1002/app.1979.07023111610.1002/app.1979.070231116 ↗
36. 10.1002/app.1979.07023111710.1002/app.1979.070231117 ↗
37. Akinlabi AK · J. Appl. Polym. Sci · 2005 · 98 · 173310.1002/app.22314 ↗
38. 10.1002/app.1270610.1002/app.12706 ↗
39. 10.1080/0360255080227469610.1080/03602550802274696 ↗
40. 10.1016/j.reactfunctpolym.2005.05.00110.1016/j.reactfunctpolym.2005.05.001 ↗