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Effect of TiO2 addition on the preparation of β-spodumene powders by sol-gel process

Published online by Cambridge University Press:  26 July 2012

Moo-Chin Wang
Affiliation:
Department of Mechanical Engineering, National Kaohsiung Institute of Technology, Kaohsiung, 80782, Taiwan, Republic of China
Ming-Hong Lin
Affiliation:
Department of Mechanical Engineering, National Kaohsiung Institute of Technology, Kaohsiung, 80782, Taiwan, Republic of China
Hok-Shing Liu
Affiliation:
Department of Mineral and Petroleum Engineering, National Cheng-Kung University, Tainan, Taiwan, Republic of China
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Extract

This study has shown the possibility of achieving two primary considerations for the advanced fabrication of spodumene with a composition of Li2O · Al2O3 · 4SiO2 · nTiO2 (LAST) glass-ceramics by a sol-gel process, namely, an enormous reduction of sintering temperature from 1600 to 1200 °C together with the appearance of simple phases of β-spodumene/rutile as opposed to products via the conventional melting-crystallization process. Fine glass-ceramic powders with a composition of Li2O · Al2O3 · 4SiO2 (LAS) have been synthesized by the sol-gel process using Si(OC2H5)4, Al(OC2H5)3, LiOCH3, and Ti(OC2H5)4 as the starting materials. The process included well-controlled hydrolysis polycondensation of the raw alkoxides. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and electron diffraction (ED) analysis were utilized to study the effect of TiO2 addition on the preparation of β-spodumene powders by the sol-gel process. The gelation time of the LAST solution increases as the TiO2 content increases. For the low (<3) or high (>11) pH value, the gelation time was shortened. At pH = 5, regardless of the TiO2 content, the gel has the longest time of gelation. When the dried gels of the LAST system are heated from 800 to 1200 °C, the crystallized samples are composed of the major phase of β-spodumene and a minor phase of rutile (TiO2).

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Copyright
Copyright © Materials Research Society 1999

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References

REFERENCES

1.Knickerbocker, S., Tuzzolo, M. R., and Lawhorne, S., J. Am. Ceram. Soc. 72, 1873 (1989).CrossRefGoogle Scholar
2.Suzuki, H., Takahashi, J., and Saito, H., J. Chem. Soc. Jpn., No. 10, 1319 (1991).Google Scholar
3.Yang, J. S., Sakka, S., Yoko, T., and Kozuka, H., J. Mater. Sci. 26, 1827 (1991).CrossRefGoogle Scholar
4.Samuneva, B., Jambazov, S., Lepkova, D., and Dimitriev, Y., Ceram. Int. 16, 355 (1990).CrossRefGoogle Scholar
5.Dislich, H., J. Non-Cryst. Solids 73, 599 (1985).CrossRefGoogle Scholar
6.Schmidt, H., J. Non-Cryst. Solids 73, 681 (1985).CrossRefGoogle Scholar
7.Johnson, D. W. Jr., Am. Ceram. Soc. Bull. 64, 1597 (1985).Google Scholar
8.Murakami, H., Yaegashi, S., Nishino, J., Shiohara, Y., and Tanaka, S., Jpn. J. Appl. Phys. 29, 2715 (1990).CrossRefGoogle Scholar
9.Colomban, Ph., Ceram. Int. 15, 23 (1989).CrossRefGoogle Scholar
10.Orcel, G. and Hench, L. L., in Science of Ceramic Chemical Processing, edited by Hench, L.L. and Ulrich, D.R. (John Wiley & Sons, New York, 1982), pp. 224230.Google Scholar
11.Wang, M. C., J. Mater. Res. 9, 2290 (1994).CrossRefGoogle Scholar
12.Girin, O. P., in The Structure of Glass, Vol. 3, Catalyzed Crystallization of Glass (Consultants Bureau Enterprises, Inc., 1964), pp. 105106.Google Scholar
13.Nakamoto, K., Infrared and Raman Spectra of Inorganic and Coordination Compounds (John Wiley & Sons, New York, 1978), p. 437.Google Scholar
14.Hamasaki, T., Eguchi, K., Koyanagi, Y., Matsumoto, A., Utsunomiya, T., and Koba, K., J. Am. Ceram. Soc. 71, 1120 (1988).CrossRefGoogle Scholar
15.Komarneni, S. and Roy, R., J. Am. Ceram. Soc. 68C, 243 (1985).Google Scholar
16.Gabelica-Robert, M. and Tarte, P., Phys. Chem. Minerals 7, 26 (1981).CrossRefGoogle Scholar
17.Mysen, B.O., Virgo, D., and Seifert, F.A., Am. Mineral. 70, 88 (1985).Google Scholar
18.McMillan, P. and Piriou, B., J. Non-Cryst. Solids 53, 279 (1982).CrossRefGoogle Scholar
19.Bogush, G.H. and Zukoski, C. F., in Ultrastructure Processing of Advanced Ceramics, edited by Mackenzie, J. D. and Ulrich, D. R. (John Wiley & Sons, New York, 1988), pp. 477486.Google Scholar
20.Brinker, C.J. and Scherer, G. W., Sol-Gel Science (Academic Press, Inc., New York, 1990), pp. 196201.Google Scholar
21.Cullity, B.D., Elements of X-ray Diffraction (Addison-Wesley, Reading, MA, 1967), p. 388.Google Scholar
22.Jarcho, M., Bolen, C.H., Thomas, M. B., Bobick, J., Kay, J.F., and Doremus, R.H., J. Mater. Sci. 11, 2027 (1976).CrossRefGoogle Scholar
23.Strnad, Z., Glass-Ceramic Materials (Elsevier, Amsterdam, 1986), pp. 6366.Google Scholar