Surface Modification of Liquid Crystal Polymers by Two Steps UV-Induced Graft Polymerization
Source abstract
Abstract
High efficiently conducting Norrish II type UV-induced graft polymerization on fully aromatic liquid crystal polymers (LCPs) is still a great change due to its lack of sp 3 hybridized C–H bonds. Here, a facile strategy for photograft modification of LCP film surfaces was developed. First, the LCP surface was modified by the UV-assisted aminolysis reaction to introduce H atoms that can be effectively abstracted by Norrish II type photosensitizers. Then, photograft polymerization of acrylic acid or styrene/maleic anhydride on the surface of modified LCP was achieved under UV irradiation by using benzophenone (BP) as a photosensitizer. The water contact angle of LCP decreased from 86° to 40° after being photografted with poly(acrylic acid) (PAA). The highest grafting density reached 7.78 × 10 –2 mg/cm 2, which is much higher than the unmodified LCP directly photografted with PAA (2.57 × 10 –3 mg/cm 2 ). The strategy showed excellent spatial controllability in preparation of the regionally modified LCP surface. Patterned polymer brushes of PAA and styrene-maleic anhydride copolymer could be introduced onto the surface of the LCP film with the help of a photomask, which were further used to selectively deposit a silver pattern by electroless plating and immobilize protein, respectively. The PAA-modified LCP deposited with the copper layer exhibited improved adhesive property with copper foil and had a peeling strength of 12.3 N/cm, which was much higher than the peeling strength of blank LCP (0.7 N/cm). This success of the two-step UV-induced graft surface modification of LCP has promising applications in the fields of high-speed electronic communication, biomedical materials, composite materials, and other fields.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Surface Modification and Superhydrophobicity · Advanced Polymer Synthesis and Characterization · Polymer Surface Interaction Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Chemical Resource Engineering
Beijing University of Chemical Technology
Beijing Laboratory of Biomedical Materials
Beijing Advanced Innovation Centre for Soft Matter Science and Engineering
Funding
Natural Science Foundation of Beijing Municipality · National Natural Science Foundation of China
References (39)
Show source-provided references
1. Sloan F. · 2017 · 11310.1016/B978-0-08-100550-7.00005-X ↗
2. 10.1016/j.aiepr.2020.10.00510.1016/j.aiepr.2020.10.005 ↗
3. 10.1002/ange.20230901010.1002/ange.202309010 ↗
4. 10.1007/s00289-023-05114-810.1007/s00289-023-05114-8 ↗
5. 10.1021/acsmaterialslett.3c0066510.1021/acsmaterialslett.3c00665 ↗
6. 10.1080/02678292.2020.178194210.1080/02678292.2020.1781942 ↗
7. 10.1080/02678292.2019.167990110.1080/02678292.2019.1679901 ↗
8. Kim T. H. · Curr. Opt. Photonics · 2019 · 3 · 66
9. 10.1080/15421406.2017.128960410.1080/15421406.2017.1289604 ↗
10. 10.1002/adom.20180025010.1002/adom.201800250 ↗
11. 10.1021/acsami.1c2510310.1021/acsami.1c25103 ↗
12. 10.1002/adom.20200174310.1002/adom.202001743 ↗
13. 10.1038/nmat201010.1038/nmat2010 ↗
14. 10.1039/C7SM01949A10.1039/C7SM01949A ↗
15. Hegmann, E.; Prévôt, M. E.; Hegmann, T. Biodegradable, biocompatible 3D liquid crystal elastomeric foam scaffolds having tailor-made animal (human) pore cell sizes via a salt leaching method are capable of growing tissue therein for therapeutic reconstruction of damaged and/or diseased tissue or organs, U.S. Patent No. 10,709,815, 2020.
16. 10.1016/j.vacuum.2006.05.00910.1016/j.vacuum.2006.05.009 ↗
17. 10.1007/s10853-005-2681-510.1007/s10853-005-2681-5 ↗
18. 10.1002/polb.1040710.1002/polb.10407 ↗
19. 10.1039/C6RA17729H10.1039/C6RA17729H ↗
20. Walles, W. E.; Nowak, R. M. Process Improve Adhesion of PBO and PBT Fibers in a Matrix resin. Patent Number IE920506A1, 1992.
21. 10.1007/s12221-013-0059-x10.1007/s12221-013-0059-x ↗
22. 10.1002/pc.2060310.1002/pc.20603 ↗
23. 10.1016/j.matlet.2017.10.09910.1016/j.matlet.2017.10.099 ↗
24. 10.1016/j.apsusc.2011.10.11110.1016/j.apsusc.2011.10.111 ↗
25. 10.1016/j.polymer.2015.02.05610.1016/j.polymer.2015.02.056 ↗
26. 10.1038/pj.2016.2410.1038/pj.2016.24 ↗
27. 10.3390/polym1110163110.3390/polym11101631 ↗
28. 10.1038/140195b010.1038/140195b0 ↗
29. 10.1021/ma951554310.1021/ma9515543 ↗
30. 10.1016/j.progpolymsci.2008.06.00210.1016/j.progpolymsci.2008.06.002 ↗
31. 10.1016/j.polymer.2011.07.02710.1016/j.polymer.2011.07.027 ↗
32. 10.1002/(SICI)1097-4628(19961017)62:3<545::AID-APP12>3.0.CO;2-Y10.1002/(SICI)1097-4628(19961017)62:3<545::AID-APP12>3.0.CO;2-Y ↗
33. 10.1002/adfm.20040033510.1002/adfm.200400335 ↗
34. 10.1021/la701126t10.1021/la701126t ↗
35. 10.1016/j.apsusc.2023.15914410.1016/j.apsusc.2023.159144 ↗
36. 10.4028/www.scientific.net/amr.311-313.180210.4028/www.scientific.net/amr.311-313.1802 ↗
37. 10.1002/app.5264410.1002/app.52644 ↗
38. 10.1039/D0NA00176G10.1039/D0NA00176G ↗
39. 10.1021/am100016310.1021/am1000163 ↗