High Transparency and Thermal Stability of Alicyclic Polyimide with Crosslinking Structure by Triallylamine

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Abstract:

Colorless alicyclic polyimides (ALPIs) were synthesized from an alicyclic dianhydride, bicyclo[2.2.2]oct-7-ene-2,3,5,6-tetracarboxylic dianhydride (BCDA) and an aromatic diamine, 3,4'-oxydianiline (3,4'-ODA). For comparison, a series of crosslinkable ALPI membranes with different content of crosslinkable reagents were prepared. The crosslinkable PI reacts with the crosslinkers and forms covalent bond to create the crosslink structure between PI backbones by free radical reaction. Almost of the crosslinkable PIs exhibit excellent dimensional stability and higher transparency because of the crosslink structure and non-conjugate alicyclic chain. All of the crosslink ALPIs could be coated into flexible and tough films. They had a UV-Vis cut-off at 297 nm and a transmittance of higher than 80% in near ultraviolet region. These PIs show low coefficient of thermal expansion ranging from 57.36 to 47.53 ppm/°C, the glass transition temperature in the range of 336.2-333.0 °C, the decomposition temperature in the range of 433.7-440.0 °C. The crosslinkable ALPIs show excellent optical properties with the excited wavelength ranging from 340 to 328 nm and stronger emission intensity than linear PI, the haze lower than 0.7, the refractive index about 1.6 and the abbe numbers over 165.

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Advanced Materials Research (Volumes 287-290)

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1388-1396

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July 2011

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© 2011 Trans Tech Publications Ltd. All Rights Reserved

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[1] P.M. Hergenrother, K.A. Watson, J.G Smith Jr, J.W. Connell and R. Yokota: Polym. Vol. 43 (2002), p.5077

Google Scholar

[2] C.P. Ying and Y.Y. Su: Polymer Vol. 46 (2005), p.5778

Google Scholar

[3] J. Yan, Z. Wang, L. Gao, and M. Ding: Macromolecules Vol. 39 (2006), p.7555

Google Scholar

[4] J.G. Liu, G.L. Wu, Z.B. Li, H.S. Li, L. Fan and S.Y. Yang: Chin. J. Polym. Sci. Vol. 22 (2004), p.511

Google Scholar

[5] D.J. Liaw, C.C. Huang and W.H. Chen: Polymer Vol.47 (2006), p.2337

Google Scholar

[6] M. Hasegawa, I. Mita, M. Kochi, and R. Yokota: J. Polym. Sci., Part C : Polym. Lett. Vol. 25 (1989), p.263

Google Scholar

[7] R. Reuter, H. Franke, and C. Feger: Appl. Optics Vol. 27 (1988), p.4565

Google Scholar

[8] C. Feger, R. Reuter and H. Franke: Polym. Prepr. (ACS Div. Polym. Chem.) Vol. 29 (1988), p.242

Google Scholar

[9] M. Hasegawa, Y. Shindo, T. Sugimura, S. Ohshima, K. Hone, M. Kochi, R. Yokota, and I. Mita: J. Polym. Sci. Part B : Polym. Phys. Vol. 31 (1993), p.1617

DOI: 10.1002/polb.1993.090311118

Google Scholar

[10] Y. Tokita, Y. Ino, A. Okamoto, M. Hasegawa, Y. Shindo, and T. Sugimura: Kobunshi Ronbunshu Vol. 51 (1994), p.245

Google Scholar

[11] M.C. Choi, J. Wakita, C.S. Ha and S. Ando: Macromolecules Vol. 42 (2009), p.5112

Google Scholar

[12] T. Matsumoto and C. Feger: J. Photopolym. Sci. Technol. Vol. 11 (1998), p.231

Google Scholar

[13] I.K. Spiliopoulos, J.A. Mikroyannidis and G.M. Tsivgoulis: Macromolecules Vol. 31 (1998), p.522

Google Scholar

[14] D.J. Liaw, B.Y. Liaw and J.M. Tseng: J Polym Sci, Part A: Polym Chem Vol. 37 (1999) p.2629

Google Scholar

[15] D.J. Liaw, P.N. Hsu, W.H. Lin and S.L. Chen: Macromolecules Vol. 35 (2002), p.4669

Google Scholar

[16] D.J. Liaw, B.Y. Liaw, P.N. Hsu and C.Y. Hwang: Chem. Mater. Vol. 13 (2001), p.1811

Google Scholar

[17] G. Rabilloud, in: Polyquinoxalines and polyimides, page 199 of High-performance polymers 2, Paris: Editions Technip (1999).

Google Scholar

[18] D.J. Liaw, F.C. Chang, M.K. Leung, M.Y. Chou and K. Muellen: Macromolecules Vol. 38 (2005), p.4024

Google Scholar

[19] D.J. Liaw, B.Y. Liaw and M.Q. Jeng: Polymer Vol. 39 (1998), p.1597

Google Scholar

[20] D.J. Liaw, W.H. Chen and C.C. Huang In: Polyimides and other high temperature polymers, Editor by K.L. Mittal, volume 2, Utrecht: VSP (2003).

Google Scholar

[21] X. Jin and D. Zhu: Eur. Polym. J. Vol. 44 (2008), p.3571

Google Scholar

[22] X. Jin, D. Zhu, A. Zhang, X. Han and Z. Qing: proceeding of SPIE Vol. 5279 (2004), p.303

Google Scholar

[23] I.H. Choi and J.H. Chang: Polymer(Korea) Vol. 34 (2010), p.391

Google Scholar

[24] M. Hasegawa and K. Horie: Prog. Polym. Sci. Vol. 26 (2001), p.259

Google Scholar

[25] S. Meyer, P. Pescador and E. Donath: J. Phys. Chem. C Vol. 112 (2008), p.1427

Google Scholar

[26] V. Arun, P.P. Robinson, S. Manju, P. Leeju, G. Varsha, V. Digna and K.K.M. Yusuff: Dyes Pigments Vol. 82 (2009), p.268

DOI: 10.1016/j.dyepig.2009.01.010

Google Scholar

[27] D. Chandra and A. Bhaumik: J. Mater. Chem.Vol. 19 (2009), p. (1901)

Google Scholar

[28] F. Salehli, O. Kamer, H. atalgil-Giz, A. Giz and G. Yıldız: J. Non-Cryst. Soilds Vol. 305 (2002), p.183

DOI: 10.1016/s0022-3093(02)01105-5

Google Scholar

[29] M.H. Tsai and W.T. Whang: J. Appl. Polym. Sci. Vol. 81 (2001), p.2500

Google Scholar

[30] K.W. Lee, S.H. Paek, A. Lien, C. Durning, H. Fukuro: Polym. Prepr. Vol. 38 (1997), p.372

Google Scholar