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Design of Novel Treated Silica Xerogels: Synthesis, Property and Reinforcement in Silicone Elastomers

Published online by Cambridge University Press:  10 February 2011

Q. Deng
Affiliation:
Dow Coming Corporation, Midland, MI 48686-0994
G. T. Bums
Affiliation:
Dow Coming Corporation, Midland, MI 48686-0994
J. R. Hahn
Affiliation:
Dow Coming Corporation, Midland, MI 48686-0994
C. C. Reese
Affiliation:
Dow Coming Corporation, Midland, MI 48686-0994
J. D. Preston
Affiliation:
Dow Coming Corporation, Midland, MI 48686-0994
S. B. Winchell
Affiliation:
Dow Coming Corporation, Midland, MI 48686-0994
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Abstract

Treated silica xerogels with controlled porosity and surface area were prepared by the in-situ treatment of hydrogels with hexamethyldisiloxane in the presence of isopropyl alcohol. The resulting hydrogels were hydrophobic and readily transferred to organic solvents allowing their isolation. The surface area and porosity of the xerogel were controlled by varying the pH, time and temperature used to aggregate the hydrogel prior to treatment. The treated xerogels were evaluated as reinforcing fillers in silicone rubber formulations. When the bases were crosslinked with peroxides, silicone elastomers with acceptable mechanical properties were obtained. The relationship between the surface area, porosity and the type and degree of surface treatment of the xerogel, and its reinforcing ability was studied. In general, the mechanical properties of the elastomer increased as the filler structure increased; however, xerogels with higher surface areas were more difficult to incorporate and gave higher plasticity bases.

Type
Research Article
Copyright
Copyright © Materials Research Society 1998

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References

REFERENCES

1. Rothon, R., Particulate-Filled Polymer Composites, Longman Scientific & Technical, England, 1995.Google Scholar
2. Clarson, S., McCarthy, D. andMark, J., Polymer Preprints (Am. Chem. Soc., Div. Polym. Chem.) 30, pp. 298–99 (1989).Google Scholar
3. Wen, J. andMark, J., J. Appl. Polym. Sci. 58, pp. 11351145 (1995).Google Scholar
4. Visser, S., J. Applied Poly. Sci. 65, p. 1805 (1997).Google Scholar
5. Visser, S., J. Applied Poly. Sci. 65, p. 1443 (1997).Google Scholar
6. Visser, S., Hewitt, C. E. andBinga, T. D., J. Applied Poly. Sci., Part B: Polym. Phys. 34, pp. 16791689 (1996).Google Scholar
7. Zaborski, M., Slusarski, L., Donnet, J. -B., Papirer, E., and Lodz, E., Kautsch Gummi Kunstst. 47, pp. 730–8 (1994).Google Scholar
8. Rigbi, Z., Haifa, I., Kautsch Gummi, Kunstst. 42, pp. 11071110 (1989).Google Scholar
9. Morton, M., Adv. Chem. Ser. 99, pp. 490509 (1971).Google Scholar
10. Polmanteer, K. E., Lentz, C. W., Rubber Chem. and Technology, 48, pp. 795809 (1974).Google Scholar
11. Herrmann, G., Nimitz, F., Faulhaber, H., Kautsch. Gummi Kunstst. 49, pp. 289292 (1996).Google Scholar
12. Casstaing, J. C., Allain, C., Auroy, L., Auvray, L. andPouchelon, A., Europhysics Letters, 36, pp. 153158 (1996).Google Scholar
13. Pu, Z. andMark, J., Chem. Mater. 9, pp. 24422447 (1997).Google Scholar
14. Lentz, C., Patent, U.S. No. 3,122,520. Issued Feb. 25, 1964.Google Scholar
15. Bondi, A., J. Phys. Chem. 68, p. 441 (1964).Google Scholar
16. Karsek, L., International Polymer Sci. and Techn. 21, pp. 3540 (1994).Google Scholar