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Preparation and Properties of Poly(Phenyleneterephthalamide)-Silica Ceramers With Interphase Bonding From Aminophenyltrimethoxysilane

Published online by Cambridge University Press:  21 February 2011

Z. Ahmad
Affiliation:
PPG Industries, Inc., 440 College Park Drive, Monroeville, PA 15146.
S. Wang
Affiliation:
Department of Chemistry, Quaid-I-Azam University, Islamabad 45320, Pakistan.
J. E. Mark
Affiliation:
Department of Chemistry and the Polymer Research Center, The University of Cincinnati, Cincinnati, OH 45221–0 172, USA
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Abstract

Poly(phenyleneterephthalamide) chains having carbonyl chloride end groups were prepared by reacting a mixture of m- and p--phenylene diamines with terephthaloyl chloride, and were then end-capped with aminophenyl-trimethoxysilane. The polymer thus prepared was used to synthesize a hybrid material in which it was chemically bonded to a silica network produced in-situ by hydrolyzing tetramethoxysilane. Films prepared from this hybrid material were yellow but transparent, and quite tough. The transparency of the films and their mechanical strength were considerably improved relative to the corresponding systems in which the inorganic network was not bonded to the organic phase. Tensile strength was found to increase initially with addition of silica but then to decrease rapidly with further additions. Elongation at rupture also decreased after an initial small increase. A systematic increase in the tensile modulus and hardness with increase in the silica content and a decrease in water absorption were also observed. SEM analysis showed that the silica particle size depends on the silica content, and was 0.5 μm or less. These transparent ceramers were found to withstand tensile stresses the order of 175 MPa and had thermal decomposition temperatures around 460 - 475 ° C, and could thus be very useful in engineering applications at high temperatures.

Type
Research Article
Copyright
Copyright © Materials Research Society 1998

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References

REFERENCES

1 Schmidt, H., Mater. Res. Soc. Svmp. Proc.. 180, 961 (1990).Google Scholar
2 Brinker, C.J. and Scherer, G.W., “Sol-Gel Science: the Physics and Chemitry of Sol-Gel Processing”, Academic Press, Boston, 1990.Google Scholar
3 Hench, L.L. and West, J.K., Chem. Rev.. 90, 33 (1990).Google Scholar
4 Brinker, C.J. et al. (ed), “Better Ceramics through Chemistry”, Vol II, III., Materials Research Society, Pittsburgh, PA, 1986, 1988.Google Scholar
5 Klein, L.C. (ed.), “Sol-Gel Technology for Thin Films, Preforms, Electronics, and Specialty Shapes”, Noyes, Park Ridge, NJ, 1988.Google Scholar
6 Langley, N.R., Mbah, G.C., Freeman, H.A., Huang, H., Siochi, E.J., Ward, T.C. and Wilkes, G.L., J. Colloid Interface Sei.. 143, 309 (1991).Google Scholar
7 Huang, H.-H., Orer, B. and Wilkes, L., Polvm. Bull.. 14, 557 (1985).Google Scholar
8 Huang, H.-H., Orler, B. and Wilkes, L., Macromolecules. 20, 1322 (1987).Google Scholar
9 Spinu, M., Brennan, A., Rancourt, J., Wilkes, G.L. and McGrath, J.E., Mater. Res. Soc. Svm. Proc.. 175, 179 (1990).Google Scholar
10 Wang, B., Wilkes, G.L., Smith, CD. and McGrath, J.E., Polvmer Commun.. 32, 400 (1991)Google Scholar
11 Mauritz, K.A. and Jones, C.K., J. Appl. Polvm. Sei.. 40, 1401 (1990).Google Scholar
12 Wang, B., Wilkes, G.L., Hedrick, J.C., Liptak, S.C. and McGrath, J.E., Macromolecules. 24, 3449 (1990).Google Scholar
13 Nandi, M., Conklin, J.A., Salvati, L. Jr. and Sen, A., Chem. Mater.. 3, 201 (1991).Google Scholar
14 Glaster, R. H. and Wilkes, G.L., Polvm. Bull.. 22, 527 (1989).Google Scholar
15 Philipp, G. and Schmidt, H., J. Non-Crvst. Solids. 82, 31 (1986).Google Scholar
16 Morikawa, A., Iyoku, Y., Kakimoto, M. and Imai, Y., Polvm. J.. 24, 107 (1992).Google Scholar
17 Nandi, M., Conklin, J.A., Salvati, L. Jr. and Sen, A., Chem. Mater.. 2, 772 (1990).Google Scholar
18 Wang, S., Ahamd, Z. and Mark, J.E., Polvm. Bull.. 31, 323 (1993).Google Scholar
19 Morgan, W., J. Polvm. Sei.. Part C. 4, 1075 (1963).Google Scholar
20 Higassui, F., Ogata, S.I. and Aoki, Y., J. Polvm. Sei.. Polvm. Chem Ed.. 20, 2085 (1982).Google Scholar