Hostname: page-component-848d4c4894-8kt4b Total loading time: 0 Render date: 2024-06-26T15:43:23.050Z Has data issue: false hasContentIssue false

Rigid-Rod And Segmented Rigid-Rod Polyimides: GEL/SOL And Liquid Crystalline Transitions, Fibers And Films

Published online by Cambridge University Press:  15 February 2011

Stephen Z. D. Cheng
Affiliation:
Institute and Department of Polymer Science, University of Akron, Akron, OH 44325–3909
Fred E. Arnold Jr.
Affiliation:
Institute and Department of Polymer Science, University of Akron, Akron, OH 44325–3909
Mark Eashoo
Affiliation:
Institute and Department of Polymer Science, University of Akron, Akron, OH 44325–3909
Song-Koo Lee
Affiliation:
Institute and Department of Polymer Science, University of Akron, Akron, OH 44325–3909
Steve L. C. Hsu
Affiliation:
Institute and Department of Polymer Science, University of Akron, Akron, OH 44325–3909
Chul Joo Lee
Affiliation:
Institute and Department of Polymer Science, University of Akron, Akron, OH 44325–3909
Frank W. Harris
Affiliation:
Institute and Department of Polymer Science, University of Akron, Akron, OH 44325–3909
Get access

Abstract

Organo-soluble rigid-rod and segmented rigid-rod polyimides and their copolyimides exhibit isotropic solutions in hot m-cresol, but form gels upon cooling. A lyotropic liquid crystal phase is observed below the gel/sol transition. Mechanical gel formation is caused by liquid-liquid phase separation, while the liquid crystal phase may be formed through a nucleation process after gelation. High performance fibers can be spun from the hot isotropic solutions using a dry-jet wet spinning method. After the fibers are drawn at high temperatures, they display tensile strength higher than 3.2 GPa and an initial modulus higher than 130 GPa. In particular, the fibers retain relatively high mechanical properties at elevated temperatures. Solution casted films exhibit very low thermal expansion coefficients and dielectric constants. Their structure, morphology and property relationships will also be discussed.

Type
Research Article
Copyright
Copyright © Materials Research Society 1991

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

[1] Lee, H., Stoffey, D. and Neville, K., in New Linear Polymers (McGraw Hill, New York, 1967), pp. 183 224.Google Scholar
[2] Sroog, C.E., J. Polym. Sci. Macromol. Rev., 11, 161 (1976).Google Scholar
[3] Harris, F.W. and Hsu, S.L.-C., High Perform. Polym., 1, 1 (1989).CrossRefGoogle Scholar
[4] Cheng, S.Z.D., Lee, S.K., Barley, J.S., Hsu, S.L.-C. and Harris, F.W., Macromolecules, 24, 1883 (1991).Google Scholar
[5] Cheng, S.Z.D., Wu, Z.-Q., Eashoo, M., Hsu, S.L.-C. and Harris, F.W., Polymer, in press.Google Scholar
[6] Arnold, F.E. Jr., Cheng, S.Z.D., Lau, S.-F., Hsu, S.L.-C. and Harris, F.W., Manuscript in preparation.Google Scholar
[7] Cheng, S.Z.D., Arnold, F.E. Jr.,, Zhang, A.-Q., Hsu, S.L.-C. and Harris, F.W., Macromolecules, in press.Google Scholar