Synthesis and Characterization of Polyimides Derived from Novel 1,3-Bis(4-Aminophenoxy)Benzene

Article Preview

Abstract:

A novel aromatic ether diamine 1,3-bis(4-aminophenoxy)benzene (TPER) was synthesized. Four kinds of polyimides were prepared with obtained TPER, 4,4’-diaminodiphenyl(ODA), pyromellitic dianhydride (PMDA) and end capped with phthalic anhydride(PA). The imidization process was solution imidization followed by solid-phase thermal imidization. The results of DSC, 1H-NMR and FTIR analysis showed that high purity TPER had been successfully synthesized. FTIR spectras of polyimides indicated the imidization process could reduce the final imidization temperature. The inherent viscosities([η]) showed molecular weight could be controlled via the introduction of flexible diamine and end capping agent. And all polyimides exhibited excellent thermal stability.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 199-200)

Pages:

13-18

Citation:

Online since:

February 2011

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2011 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] Adrova, N.A., M.I. Bessonov, L.A. Laius, and A.P. Rudakovetc. (1970). Polyimides (A New Class of Thermally Stable Polymers). Stanford: Technomic Publishing Co.

DOI: 10.1002/pol.1971.110090315

Google Scholar

[2] Kim, J.H., H.N. Jang, and J.Y. Lee. (2008). Polym. Bull. 60, 181-189.

Google Scholar

[3] Niyogi, S., B. Adhikari. (2002). Eur. Polym. J. 38, 1237-1243.

Google Scholar

[4] Sager, K., A. Schroth, A. Nakladal, and G. Gerlach. (1996). Sens. Actuators A: Physical. 53, 330-334.

Google Scholar

[5] Patterson, D.A., A. Havill, and S. Costello. (2009). Sep. Purif. Methods. 66, 90-97.

Google Scholar

[6] Kumar, D., A.D. Gupta. (1992). Polym. Adv. Technol. 3, 1-7.

Google Scholar

[7] Tamai, S., A. Yamaguchi, and M. Ohta. (1996). Polymer. 37, 3683-3692.

Google Scholar

[8] Tamai, S., T. Kuroki, A. Shibuya, and A. Yamaguchi. (2001). Polymer. 42, 2373-2378.

Google Scholar

[9] Sasaki, T., H. Morinchi, S. Yano, and R. Yokota. (2005). Polymer. 46, 6968-6975.

Google Scholar

[10] Kuroki, T., A. Shibuya, M. Toriida, and S. Tamai. (2004). J. Polym. Sci., Part A: Polym. Chem. 42, 2395-2404.

DOI: 10.1002/pola.20079

Google Scholar

[11] Zhou, H.W., C. Chen, R. Kanbara, T. Sasaki, and R. Yokota. (2005). High Perform. Polym. 17, 193-212.

Google Scholar

[12] Zhou, H.W., C. Chen, R. Kanbara, T. Sasaki, and R. Yokota. (2005). High Perform. Polym. 17, 213-224.

Google Scholar

[13] Meyer, G.W., S.J. Pak, Y.J. Lee, and J.E. McGrath. (1995). Polymer. 36, 2303-2309.

Google Scholar

[14] Tamai, S., M. Ohta, and A. Yamaguchi. (1993). U.S. Patent 5, 268, 446.

Google Scholar

[15] Lee, K.H., J.C. Jung. (1998). Polym. Bull. 40, 407-414.

Google Scholar

[16] Jung, J.C., S.B. Park. (1995). Polym. Bull. 35, 423-430.

Google Scholar

[17] Sun, Z.H., H.Y. Li, Y.G. Zhuang, M.X. Ding, and Z.L. Feng. (1991). Polym. Bull. 26, 557-563.

Google Scholar