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Mechanisms of Al and titania hydrogel complex formation via a mechanical route

Published online by Cambridge University Press:  31 January 2011

Yuumi Kojima
Affiliation:
Institute for Materials Research, Tohoku University, Katahira, Sendai 980, Japan
Tetsuhiko Isobe
Affiliation:
Institute for Materials Research, Tohoku University, Katahira, Sendai 980, Japan
Mamoru Senna*
Affiliation:
Institute for Materials Research, Tohoku University, Katahira, Sendai 980, Japan
Takeshi Shinohara
Affiliation:
Faculty of Science and Technology, Keio University, Hiyoshi, Yokohama 223, Japan
Sakai Ono
Affiliation:
Faculty of Science and Technology, Keio University, Hiyoshi, Yokohama 223, Japan
Kenji Sumiyama
Affiliation:
Faculty of Science and Technology, Keio University, Hiyoshi, Yokohama 223, Japan
Kenji Suzuki
Affiliation:
Faculty of Science and Technology, Keio University, Hiyoshi, Yokohama 223, Japan
*
a) Author to whom all correspondence should be addressed.
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Abstract

The process of complex formation has been studied during milling a powder mixture of metallic Al and titania hydrogel, TiO2 · H2O. Solid state 27Al NMR and ESR are employed together with conventional x-ray diffractometry and thermal analyses. Al atoms partly changed from metallic to oxide state. 27Al NMR analyses indicate that two metallic Al states are allotted to distorted and undistorted lattices, while the other to AlOx units in the oxide state, where x is 4, 5, or 6. As detected by ESR, Ti4+ was partly reduced to Ti31, suggesting a redox reaction during milling. A vigorous thermit reaction was detected during subsequent heating of the mixture after prolonged milling. These results indicate the formation of Al–O–Ti bonds during milling, leading to Al2TiO5 on subsequent heating.

Type
Articles
Copyright
Copyright © Materials Research Society 1996

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References

REFERENCES

1.Kojima, Y., Isobe, T., Senna, M., El-Eskandarany, M.S., Sumiyama, K., and Suzuki, K., Int. J. Mechanochem. Mech. Alloying 1, 34 (1994).Google Scholar
2.Kojima, Y., Senna, M., Shinohara, T., Ono, S., Sumiyama, K., and Suzuki, K., J. Alloys Compounds 227, 97 (1995).Google Scholar
3.Watanabe, T., Liao, J., and Senna, M., J. Solid State Chem. 115, 390 (1995).Google Scholar
4.Okamoto, Y., Isobe, T., and Senna, M., J. Non-Cryst. Solids 180, 171 (1995).Google Scholar
5.Kim, D. G., Kaneko, J., and Sugamata, M., J. Jpn. Inst. Metals 57, 679 (1993).CrossRefGoogle Scholar
6.Takacs, L., Mater. Lett. 13, 119 (1992).Google Scholar
7.Takacs, L., Nanostructured Mater. 2, 241 (1993).CrossRefGoogle Scholar
8.Takacs, L., in Nanophase and Nanocomposite Materials, edited by Komarneni, S., Parker, J.C., and Thomas, G.J. (Mater. Res. Soc. Symp. Proc. 286, Pittsburgh, PA, 1993), p. 413.Google Scholar
9.Lang, S. M., Fillmore, C.L., and Maxwell, L.H., J. Res. Natl. Bur. Stand. 48, 298 (1952).CrossRefGoogle Scholar
10.Carter, G. C., Bennett, L. H., and Kahan, D. J., Prog. Mater. Sci. 20, Metallic Shifts in NMR Part I (1977), p. 134.Google Scholar
11.Lawrence, B. and Kirker, G. W., J. Am. Chem. Soc. 108, 6158 (1986).Google Scholar
12.Serwicha, E., Schindler, R.N., and Shumacher, R., Ber. Bunsenges. Phys. Chem. 85, 192 (1981).CrossRefGoogle Scholar
13.Duran, A., Wohlfromm, H., and Pena, P., J. Europ. Ceram. Soc. 13, 73 (1994).CrossRefGoogle Scholar