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Microwave Drying of Borosilicate Gels

Published online by Cambridge University Press:  28 February 2011

Srinivas Surapanani
Affiliation:
Department of Chemistry and Chemical Engineering Michigan TechnologicalUniversity Houghton, MI 49931
Michael E. Mullins
Affiliation:
Department of Chemistry and Chemical Engineering Michigan TechnologicalUniversity Houghton, MI 49931
B.C. Cornilsen
Affiliation:
Department of Chemistry and Chemical Engineering Michigan TechnologicalUniversity Houghton, MI 49931
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Abstract

Microwave processing was carried out on SiO2 -B2O3 solutions and gels prepared by sol-gel methods. Monolithic gels were prepared from alcoholic solutions of trimethylborate and tetraethylorthosilicate using a two-step hydrolysis process. A novel technique of Liquid State Processing (LSP) was employed for the first time, and it was found to be faster and more effective than the conventional processing techniques. The structural evolution of the dried products was followed using FTIR. The effect of processing was examined via surface area analysis (BET), electron microscopy, and FTIR. The microwave drying has been compared with conventional oven drying and vacuum drying techniques. Shorter processing times, improved microstructures, and unique properties have been obtained.

Type
Research Article
Copyright
Copyright © Materials Research Society 1991

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References

REFERENCES

1. Sutton, W. H., “Microwave Processing of Ceramic Materials,” Ceramic Bulletin, 68, 376385 (1989).Google Scholar
2. Roy, R., Komarneni, S., and Yang, L. J., “Controlled Microwave Heating and Melting of Gels,” J. Am. Ceram. Soc., 68, 392395 (1985).Google Scholar
3. Yoldas, B. E., “Modification of Polymer-Gel Structures,” J. Non. Crvs. Sol. 63, 145154 (1984).Google Scholar
4. Villegas, M. A., and Navarro, J. M. Fernandez, “Characterization of B2 0 3 -SiO2 Glasses Prepared Via Sol-Gel”, J. Mat. Sci., 23, 24642478 (1988).Google Scholar
5. Prassas, M., and Hench, L. L., Ultrastructure Processing of Ceramics, Glasses and Composites (Hench, L. L. and Ulrich, D. R., Eds.), Wiley, New York, 1984 p.100.Google Scholar
6. Wood, D. L., and Rabinovich, E. M., “Study of Alkoxide Silica Gels by Infrared Spectroscopy,” Applied Spectroscomv, 43, 263–67 (1989).Google Scholar
7. Orcel, G., and Hench, L. L., “Physical-Chemical Variables in Processing Na 2 0-B 2 0 3 -SiO2 Gel Monoliths,” Mat. Res. Soc. Symp. Proc., 32, 79 (1984).Google Scholar
8. Halland, D. M., and Brinker, C. J., “In Situ FTIR Studies of Oxide and Oxynitride Sol-Gel Derived Thin Films,” Mat. Res. Soc. Symp. Proc., 32, 267273 (1984).Google Scholar
9. Murray, J. W., “Sol-Gel Processing of Glass Powders,” Advances in Ceramics, Vol.21:Ceramic Powder Science (Messing, G. L., Mazdiyasni, K. S., McCauley, J. W., and Haber, R. A., Eds.), Am. Ceram. Soc., Westerville, OH, 1987.Google Scholar
10. Iler, R. K., The Colloid Chemistry of Silica and Silicates, Cornell University Press, New York, 1955.Google Scholar
11. Brinker, C. J., Drotning, W. D., and Scherer, G. W., “A Comparison Between the Densification Kinetics of Colloidal and Polymeric Silica Gels,” Mat. Res. Soc. Symp. Proc., 32, 2532 (1984).Google Scholar