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Thermochemistry of the Amorphous System SiO2-GeO2: Comparision of Flame Hydrolysis Materials to High Temperature Fused Glasses

Published online by Cambridge University Press:  21 February 2011

P. D. Maniar
Affiliation:
Dept. of Geological and Geophysical Sciences, Princeton University, Princeton, NJ 08544.
A. Navrotsky
Affiliation:
Dept. of Geological and Geophysical Sciences, Princeton University, Princeton, NJ 08544.
C. W. Draper
Affiliation:
AT&T, Engineering Research Center, Princeton, NJ 08540.
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Abstract

Energetics and structure of germania doped silica prepared from high temperature melts and by flame hydrolysis were investigated using transposed temperature drop and solution calorimetry. Heat contents (H973-H298) are similar for first and second drops for the flame hydrolysis preforms reflecting the effect of temperature of deposition (1073 K) in creating a relaxed structure which is not easily rearranged. Heats of solution, at 973 K in molten lead borate, of fused glasses along the SiO2-GeO2 binary show ideal heats of mixing between the endmembers. This'indicates that fused glasses behave in a simple manner, with ideal substitution of Ge for Si in the tetrahedral framework. Flame hydrolysis samples (preform and annealed glasses) also show ideal heats of mixing. This suggests that the flame hydrolysis materials are energetically very similar to their bulk-melted counterparts. This insensitivity of energetics to preparation conditions is consistent with our previous studies on silica prepared at various temperatures [1].

Type
Research Article
Copyright
Copyright © Materials Research Society 1990

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References

1. Maniar, P.D. and Navrotsky, A., J. Non-Cryst. Solids. in press.Google Scholar
2. Riebling, E.F., J. Am. Ceram. Soc. 51, p. 406, (1968).CrossRefGoogle Scholar
3. Huang, Y.Y., Sarkar, A. and Schultz, P.C., J. Non-Cryst. Solids. 27, p. 29, (1978).CrossRefGoogle Scholar
4. Huffman, M., Navrotsky, A. and Pintchovski, F.S., J. Electrochem. Soc. 133, p.431, (1986).Google Scholar
5. Glantschnig, W.J. and Holliday, A., Appl. Optics, 26, p.983, (1987).Google Scholar
6. Rabinovich, E.M., Johnson, D.W. Jr., MacChesney, J.B. and Vogel, E.M., J. Am. Ceram. Soc., 66, p. 683, (1983).Google Scholar
7. Navrotsky, A., Phys. Chem. Min., 2, p. 89, (1977).CrossRefGoogle Scholar
8. Lapeyre, C., Petiau, J. and Calas, G., in: The Structure of Non-Crystalline Materials, eds. Gaskell, P.H.. Parker, J.M. and Davis, E.A. (International Publications Service, New York) p.42, (1982).Google Scholar
9. SK. Sharma, Matson, D.W. and Philpotts, J.A., J. Non-Cryst. Solids, 68, p. 99, (1984).Google Scholar
10. Huffman, M., Navrotsky, A. and Pintchovski, F.S., J. Electrochem. Soc. 133, p.164, (1986).Google Scholar