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Layered Silicate/Polystyrene Nanocomposite

Published online by Cambridge University Press:  15 February 2011

A. Moet
Affiliation:
Department of Macromolecular Science, Case Western Reserve University, Cleveland, OH 44106-7202
A. Akelah
Affiliation:
Department of Chemistry, Tanta University, Tanta, Egypt
A. Hiltner
Affiliation:
Department of Macromolecular Science, Case Western Reserve University, Cleveland, OH 44106-7202
E. Baer
Affiliation:
Department of Macromolecular Science, Case Western Reserve University, Cleveland, OH 44106-7202
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Abstract

Nano-composites have been prepared from Na+ and Ca++ montmorillonite (MMT) in a polystyrene matrix via chemical intercalation. Vinyl monomer-g-MMT was prepared by exchanging the mineral cation by vinylbenzyl trimethylammonium chloride, thus rendering the mineral organophilic and forming polymerizable moieties directly bonded to the lamellar surface of the mineral. Styrene was added and polymerized by free radical in selected solvents. The ratio of mineral to the bound polymer ranged from 0.3 to 1.25 (by weight) depending on the initial mineral concentration in the feed and on the solvent used. The mineral domains in the composite, measured from suspension cast film fall in the range of 150 nm to 400 nm. Measured from compression molded samples, the domains were ca. 50 nm which is much smaller than the mineral aggregate and comparable to that of the primary particle of the mineral. WAXD disclosed that the d (001) spacing of MMT in the composite ranged from 1.7 to 2.5 nm suggesting that the mineral aggregates (ca. 10 μm) were dissociated into individual layers then reassembled into lamellar nanoclusters.

Type
Research Article
Copyright
Copyright © Materials Research Society 1994

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References

REFERENCES

1. Okada, A., Kawasumi, M., Kurauchi, T. and Kamigaito, O., Polymer Preprints, 28, 447 (1987).Google Scholar
2. Fukushima, Y. and Inagali, S., J. Inclusion phenomena, 5, 473 (1987).Google Scholar
3. Kurauchi, Y., Okada, A., Kawasumi, M., Kurauchi, T. and Kamigaito, O., Clay miner., 23, 27 (1988).Google Scholar
4. Usuki, A., Kawasumi, M., Kojima, Y., Okada, A., Kurauchi, T. and Kamigaito, O., J.Mater.Res., 8, 1174 (1993).Google Scholar
5. Usuki, A., Kawasumi, M., Kojimai, Y., Okada, A., Kurauchi, T., and Kamigaito, O., J.Mater.Res., 8, 1179 (1993).Google Scholar
6. Moet, A. and Akelah, A., Materials Letters, 18, 97 (1993).Google Scholar
7. Vaia, R. A., Ishii, H. and Giannelis, E. P., Chem. Mater, 5, 1694 (1993).Google Scholar
8. Moet, A., Akelah, A., Salahuddin, N., Hiltner, A. and Baer, E., Proceedings Mater. Res. Soc., San Francisco, April 4-8, 1994.Google Scholar
9. Kojima, Y., Fukumori, K., Usuki, A. and Kurauchi, T., J. Mater. Sci. Lett., 12, 889 (1993).Google Scholar
10. Theng, B. K. G., Formation and properties of Clay-polymer Complexes, Elsevier, New York (1979).Google Scholar
11. Kelly, P., Akelah, A., Qutubuddin, S. and Moet, A., J. Mater. Sci., in press (1994).Google Scholar
12. Bryk, M. T., Goikhman, A. Sh., Skobets, I. E. and Ovcharenko, F. D., Kolloidnyi Zhurnal, 45, 1043 (1983).Google Scholar
13. Moet, A., Qutubuddin, S. and Kelly, P., “Anti-shrink Agent for Plastic Moldings”, Final Report, The Edison Materials Technology Center, Dayton, OH, October 1990.Google Scholar
14. Mering, J., Trans. Faraday Soc., 42, 205 (1946).Google Scholar
15. US Patent No. 4,889,885, December 26, 1989.Google Scholar
16. Topolkaraev, V., private communications.Google Scholar