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Anion Intercalation and Anion Exchange in Bismuth Compounds

Published online by Cambridge University Press:  11 February 2011

Masamichi Tsuji
Affiliation:
Tokyo Institute of Technology, Research Center for Carbon Recycling and Energy, Tokyo, JAPAN.
Makoto Yamaguchi
Affiliation:
Tokyo Institute of Technology, Research Center for Carbon Recycling and Energy, Tokyo, JAPAN. Institute of Research and Innovation, Kashiwa Laboratory, Chiba, JAPAN.
Satoshi Murao
Affiliation:
Tokyo Institute of Technology, Research Center for Carbon Recycling and Energy, Tokyo, JAPAN. National Institute of Advanced Industrial Science and Technology, Institute for Geo-resources and Environment, JAPAN.
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Abstract

Bismuth nitrate basic, which chemical content is given by 4BiNO3(OH)2.BiO(OH), was studied for anion-intercalation or anion-exchange properties. A crystal structure of the bismuth nitrate basic has not been known. In the present study, its XRD pattern was indexed using a possible orthorhombic system having the lattice parameters of ao=3.021(1) nm, bo=3.029(1) nm and co=0.9572(3) nm. This compound was found to incorporate CH3COO-, halides and several oxyanions including CO32-. Incorporation of these anions by this solid was evidenced by broadening of infrared absorption band by NO3-, suggesting involvement with NO3- ions. Intercalation of CO32- by the bismuth nitrate basic in full extent yielded a bismutite represented by the chemical composition Bi2O2CO3. The bismuth nitrate basic will serve as a new host for anion-intercalation and anion-exchange.

Type
Research Article
Copyright
Copyright © Materials Research Society 2003

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References

REFERENCES

Tsuji, M., Ikeda, Y., Sazarashi, M., Yamaguchi, M., Matsunami, J., and Tamaura, Y., Mat. Res. Bull., 35, 2109 (2000).Google Scholar
Tsuji, M., Solid State Ionics, 151, 385 (2002).Google Scholar
Reichle, W. T., Chemtech, 58 (1986);Google Scholar
Reichle, W. T., Solid States Ionics 22, 135 (1986).Google Scholar
4. Allmann, R., Chimia, 24, 99 (1970).Google Scholar
5. Thevenot, F., Szymanski, R., and Chaumette, P., Clays Clay Mineral., 37, 396 (1989).Google Scholar
6. Yamaoka, T., Abe, M., and Tsuji, M., Mat. Res. Bull., 24, 1183 (1989).Google Scholar
7. Tsuji, M., Matsunami, J. and Tamaura, Y., Trans. Mater. Res. Soc. Jpn., 24, 357 (1999).Google Scholar
8. Tsuji, M., Mao, G., Yoshida, T., and Tamaura, Y., J. Mater. Res., 8, 1137 (1993).Google Scholar
9. Khan, A. I. and O'Hare, D., J. Mater. Chem., 12, 3191 (2002).Google Scholar
10. Tsuji, M., Kanoh, H., and Ooi, K., Mat. Res. Soc. Symp. Proc., 658, GG6.25.1 (2001).Google Scholar
11. Greaves, C. and Blower, S. K., Mat. Res. Bull., 23(7), 1001 (1988).Google Scholar
12. Nakamoto, K., “Infrared and Raman Spectra”, Wiley Interscience, pp. 232233 (1986).Google Scholar