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Sol-Gel Networks: Fundamental Investigations of the Chemistry of Sol-Gel Silicate Glasses and Poly(Siloxane) Toughened Silicates

Published online by Cambridge University Press:  21 February 2011

M. Spinu
Affiliation:
Chemistry Department, Science and Technology Center: High Performance Polymeric Adhesives and Composites; Virginia Polytechnic Institute and State University; Blacksburg, VA 24061
J. E. Mcgrath*
Affiliation:
Chemistry Department, Science and Technology Center: High Performance Polymeric Adhesives and Composites; Virginia Polytechnic Institute and State University; Blacksburg, VA 24061
*
*To whom correspondence should be addressed.
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Abstract

The low-temperature sol-gel process opens a number of new materials possibilities for generation of glasses with predetermined properties by the incorporation of organic modifiers into the network. Polysiloxanes are potentially interesting organic modifiers for toughening and possibly surface-modifying the silicate networks. Some fundamental studies of the hydrolysis and condensation processes in a tetramethylorthosilicate (TMOS) system, in the absence of added catalyst, have been conducted using 1H and 29Si NMR. The effects of some of the reaction parameters and processing conditions for the subsequent conversion of the gel to monolithic dried gels by heat treatment have been investigated by techniques such as thermal analysis and mass spectroscopy. Procedures which employ mild pressures have been established that permit the generation of monolithic products which show greatly reduced cracking tendencies. Finally, methoxy functionalized poly(dimethylsiloxane) oligomers that can react into the sol-gel network have been prepared. The intermediates are commercially accessible and the process is scaleable. Utilization of a catalyst-free system eliminates the tendency of the siloxane modifier to undergo undesired rearrangements that are known to occur in the presence of strong acids or bases.

Type
Research Article
Copyright
Copyright © Materials Research Society 1989

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References

REFERENCES

1. Yoldas, B. E., J. Mat. Sci., 12, 1203, (1977); 14, 1843 (1979).Google Scholar
2. McGrath, J. E., Pullockaren, J. P, Riffle, J. S., Kilic, S., and Elsbernd, C. S., Ultrastructure Processing of Advanced Ceramics, edited by Machenzie, J. D. and Ulrich, D. R. (John Wiley & Sons, New York, 1988) p 55.Google Scholar
3. Aelion, R., Loebel, A., and Erich, E., J. Am. Chem. Soc., 72, 5705 (1950).Google Scholar
4. Chen, K. C., Tsuchiya, T., and Mackenzie, J. D., J. Non-Cryst. Solids, 81, 227, (1986).Google Scholar
5. McGrath, J. E., Sormani, P. M., Elsbernd, C. S., and Kilic, S., Makromol. Chem., Makrom. Symp., 6, 67, (1986).Google Scholar
6. Elsbernd, C. S., Sormani, P. M., Kilic, S., and McGrath, J. E., Polymer Preprints, 27(2), 152 (1986); I. Yilgor and J. E. McGrath, Adv. in Polymer Sci., 86, 1 (1988).Google Scholar
7. Elsbernd, C. S., Spinu, M., Kilic, S., and McGrath, J. E., Polymer Preprints, 29(1), 355, (1986).Google Scholar
8. Kelts, L. W., Effinger, N. J., and Melpolder, S. M., J. Non-Cryst. Solids, 83, 353, (1986).Google Scholar
9. Artaki, I., Sinha, S., Irwin, A. D., and Jonas, J., J. Non-Cryst. Solids, 72, 391, (1985).Google Scholar
10. Prassas, M., Phalippou, J., Zarzycki, J., J. Mater. Sci., 19, 1656, (1984).Google Scholar
11. Scherer, G. W., J. Non-Cryst. Solids, 89, 217, (1987).Google Scholar
12. Yamane, M., Aso, S., and Sakaino, T., J. Mater. Sci., 13, 865, (1978).Google Scholar
13. Zarzycki, J., J. Non-Cryst. Solids, 48, 105, (1982).Google Scholar
14. Huang, H., Orler, B., and Wilkes, G. L., Polym. Bull. 14, 557 (1985).Google Scholar
15. Huang, H. and Wilkes, G. L., Polym. Bull., 18, 455 (1987).Google Scholar
16. Huang, H., Orler, B., and Wilkes, G. L., Macromolecules, 20, 1322 (1987).Google Scholar
17. Brinker, C. J., Keefer, K. D., Schaefer, D. W., and Ashley, C. S., J. Non-Cryst. Solids, 48, 47 (1982).Google Scholar
18. Brinker, C. J., Keefer, K. D., Schaefer, D. W., Assink, R. A., Kay, B. D., and Ashley, C. S., J. Non-Cyst. Solids, 63, 45 (1984).Google Scholar
19. Assink, R. A. and Kay, B. D., Mat. Res. Soc. Symp. Proc. 32, 301 (1984).Google Scholar
20. Boonstra, A. H. and Mulder, C. A. M., J. Non-Cryst. Solids 105, 201 (1988).Google Scholar
21. Zerda, T. W. and Hoang, G., J. Non-Cryst. Solids, 109, 9 (1989).Google Scholar