Mechanically Robust and Transparent Polyamideimide Films via Consecutive Polycondensation, Amidation, Acid Removal, and Bluing Agent Addition
Source abstract
Abstract
Polyamideimides were prepared via consecutive high-temperature polycondensation imidization and amidation. The acid byproduct generated during amidation was removed using propylene oxide as a reactive additive, avoiding cumbersome purification. All of the varnishes had appropriate viscosities for film casting: 2300–6300 cP at 15 wt % concentration in a mixed solvent of γ-butyrolactone and N,N-dimethylacetamide. The solubility parameters of the obtained polymers were around 24.0 MPa1/2, close to that of N,N-dimethylacetamide; the densities and fractional free volumes of the polymer films were determined to be approximately 1.39 g/cm3 and 0.22, respectively. The polymer films were quite tough with an elastic modulus of up to 6.5 GPa and a tensile strength of up to 200 MPa, and their glass transition temperature reached 366 °C. A colorless and transparent film with a transmittance of 84.8% at 440 nm and a low yellow index of 1.77 was obtained by adding a bluing agent.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Synthesis and properties of polymers · Epoxy Resin Curing Processes · biodegradable polymer synthesis and properties
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Polymer Science and Engineering, Polymeric Nanomaterials Laboratory, Kyungpook National University, 1370 Sankyuk-dong, Buk-ku, Deagu702-701, Korea
Hansol Chemical Co., Ltd., 873 Gwahak-ro, Bongdong-eup, Wanju-gun, Jeollabuk-do565-904, Korea
References (28)
Show source-provided references
1. Edwards, W. M.Aromatic polyimides and the process for preparing them. U.S. Patent US3179634, April 20, 1965.
2. Choi C. H. · Polym. Sci. Technol. · 2012 · 23 · 296
3. 10.1016/j.jiec.2015.03.01310.1016/j.jiec.2015.03.013 ↗
4. 10.1109/ACCESS.2013.226079210.1109/ACCESS.2013.2260792 ↗
5. 10.1016/j.progpolymsci.2007.11.00410.1016/j.progpolymsci.2007.11.004 ↗
6. 10.1002/macp.20180031310.1002/macp.201800313 ↗
7. 10.1002/anie.20191026910.1002/anie.201910269 ↗
8. 10.1002/pi.307010.1002/pi.3070 ↗
9. Klein D. R. · 2013
10. Ju, C. H.; Park, H. J.; Jung, H. G.Transparent polyamide-imide resin and film using same. WO Patent WO2015/0994782015.
11. Lee, J. W.; Lim, D. J.; Ahn, J. I.; Lee, J. H.; Kim, S. I.; Kim, S. H.; Oh, D. S.; Jeong, D.Colorless and transparent polyamide-imide film, and manufacturing method therefore. WO Patent WO2017/1798772017.
12. Ryu, B. O.; Paek, K. Y.; Tae, Y. J.; Park, S. Y.; Park, Y. S.Polyamideimide copolymers and colorless and transparent polyamideimide film comprising the same. U.S. Patent US2019/0153161A12019.
13. van Krevelen D. W. · 2009
14. 10.1002/pen.76014021110.1002/pen.760140211 ↗
15. Barton A. F. · 1991
16. Bondi, A. Physical Properties of Molecular Crystals, Liquids, and Glasses; John Wiley and Sons: New York, 1968; pp 53–97.
17. 10.1002/pola.2685510.1002/pola.26855 ↗
18. 10.1016/j.polymer.2012.05.04710.1016/j.polymer.2012.05.047 ↗
19. Klein D. R. · 2013
20. 10.1021/ed072p62410.1021/ed072p624 ↗
21. 10.1039/P2983000041710.1039/P29830000417 ↗
22. Kwolek, S. L.Optically anisotropic aromatic polyamide dopes. U.S. Patent US3,671,5421972.
23. Sun, L.; Harris, F. W.; Jing, J.; Erdem, H. B.; Harvey, J. D.; Zhang, D.Aromatic polyamide films for transparent flexible substrates. U.S. Patent US2017/0022336 A12017.
24. Harris, F. W.; Zhang, D.; Sun, L.; Jing, J.; Umeda, H.; Okada, J.Aromatic polyamide films for solvent resistant flexible substrates. U.S. Patent US2014/0175683 A12014.
25. 10.1016/j.polymer.2020.12221810.1016/j.polymer.2020.122218 ↗
26. 10.1515/polyeng-2013-010010.1515/polyeng-2013-0100 ↗
27. 10.1016/j.eurpolymj.2009.01.01410.1016/j.eurpolymj.2009.01.014 ↗
28. Pyeon, B.; Yasui, M.; Sakurai, T.Polyimide film. JP6695367B22020.