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Preparation of fine Ni particles by the spray-pyrolysis technique and their film forming properties in the thick film method

Published online by Cambridge University Press:  31 January 2011

Kazuro Nagashima
Affiliation:
Department of Applied Chemistry, Faculty of Engineering, Kyushu University, 6-10-1 Hakozaki, Higashiku, Fukuoka 812, Japan
Masayoshi Wada
Affiliation:
Department of Applied Chemistry, Faculty of Engineering, Kyushu University, 6-10-1 Hakozaki, Higashiku, Fukuoka 812, Japan
Akio Kato
Affiliation:
Department of Applied Chemistry, Faculty of Engineering, Kyushu University, 6-10-1 Hakozaki, Higashiku, Fukuoka 812, Japan
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Abstract

Fine Ni particles were directly prepared from Ni(NO3)2 and NiCl2 aqueous solutions by the spray-pyrolysis technique under an H2-N2 atmosphere. Hollow Ni particles with rough surfaces were obtained at a low reaction temperature (700–900 °C). With increasing reaction temperatures from 900 °C to 1500 °C, the particles varied gradually to solid ones with a smooth surface, and the particles obtained at 1600 °C were perfectly spherical ones whose average size was ∼0.6 μm. From the point of view that aggregation free powders are considered to be good for thick film applications, Ni(NO3)2 was preferred to NiCl2 as a starting material. The perfectly spherical particles derived from Ni(NO3)2 gave a Ni film about 3 μm in thickness having sheet resistance of 37.7 mΩ · square−1.

Type
Articles
Copyright
Copyright © Materials Research Society 1990

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References

1Tunoda, S. and Yamaoka, N., Electronic Ceramics 18 (7), 33 (1987).Google Scholar
2Kato, A., Takayama, A., and Morimitsu, Y., J. Chem. Soc. Jpn. 1985, 2342 (1985).Google Scholar
3Nagashima, K., Morimitsu, Y., and Kato, A., J. Chem. Soc. Jpn. 1987, 2293 (1987).Google Scholar
4Nagashima, K., Iwaida, T., Sasaki, H., Katatae, Y., and Kato, A., J. Chem. Soc. Jpn. 1990, 17 (1990).Google Scholar
5Nagashima, K., Katatae, Y., and Kato, A., J. Jpn. Soc. Powder and Powder Metall. 36, 278 (1989).CrossRefGoogle Scholar
6Nagashima, K., Himeda, T., and Kato, A., J. Mater. Sci. (in press).Google Scholar
7 Shoei Chemical Industry Co., Ltd., Jpn. Kokai Tokkyo Koho JP 62 02, 404 (1987); Chem. Abstr. 107, 125393q (1987).Google Scholar
8Sproson, D. W. and Messing, G. L., Advances in Ceramics, Vol. 21: Ceramic Powder Science, edited by Messing, G. L., Mazdiyasni, K. S., McCauley, J. W., and Haber, R. A. (The Am. Ceram. Soc, Westerville, OH, 1987), p. 99.Google Scholar
9Hirata, Y., Memories of the Faculty of Engineering, Kagoshima University, No. 20, 73 (1984).Google Scholar
10Rang, R. J., J. Acoust. Soc. Am. 34, 6 (1962).Google Scholar