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Synthesis of Carbon/Ferrite Composite by In-Situ Pressure Pyrolysis of Organometallic Polymers

Published online by Cambridge University Press:  15 February 2011

Shin-Ichi Hirano ,
Toshinobu Yogo ,
Koichi Kikuta  and
Makoto Fukuda
Shin-Ichi Hirano
Affiliation:
Department of Applied Chemistry, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464, Japan
Toshinobu Yogo
Affiliation:
Department of Applied Chemistry, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464, Japan
Koichi Kikuta
Affiliation:
Department of Applied Chemistry, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464, Japan
Makoto Fukuda
Affiliation:
Department of Applied Chemistry, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464, Japan
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Abstract

Ferrite particle-dispersed carbon composite were synthesized by in-situ pressure pyrolysis of organometallic polymers at temperatures from 500 to 700°C under 125 MPa. Magnetite-dispersed carbon composite could be prepared from 550 to 700°C at 125 MPa. Nickel and nickel zinc ferrite particles were dispersed in carbon matrices at 550°C and 500°C, respectively, under 125 MPa. The morphology of the carbon matrix can be controlled by the pyrolysis conditions and the amount of coexistent supercritical water. Carbon spherulites of several micrometers dispersed with ferrite particles less than 100 nm were successfully synthesized by pressure pyrolysis of organometallic polymers in the presence of supercritical water. The saturation magnetization of magnetite-, nickel ferrite- and nickel zinc ferrite-dispersed carbon were 74, 30 and 65 emu/g, respectively. The coercive force of nickel ferrite-dispersed carbon was about 200 Oe.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 274: Symposium R – Submicron Multiphase Materials , 1992 , 167
Copyright
Copyright © Materials Research Society 1992

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References

REFERENCES

[1] Hirano, S., Dachille, F. and Walker, P.L. Jr, High Temp. High Press. 5 207 (1973).Google Scholar
[2] Hirano, S., Ozawa, M. and Naka, S., J. Mater. Sci. 16 1989 (1981).Google Scholar
[3] Hirano, S., Yogo, T., Suzuki, H. and Naka, S., J. Mater. Sci. 18 2811 (1983).Google Scholar
[4] Yogo, T., Naka, S. and Hirano, S., J. Mater. Sci. 24 2071 (1989).Google Scholar
[5] Hirano, S., Yogo, T., Nogami, N. and Naka, S., J. Mater. Sci. 21 225 (1986).Google Scholar
[6] Yogo, T., Tamura, E., Naka, S. and Hirano, S., J. Mater. Sci. 21 941 (1986).Google Scholar
[7] Yogo, T., Yokoyama, H., Naka, S. and Hirano, S., J. Mater. Sci. 21 2571 (1986).Google Scholar
[8] Yogo, T., Naka, S. and Hirano, S., J. Mater. Sci. 24 2115 (1989).CrossRefGoogle Scholar
[9] Yogo, T., Naka, S. and Hirano, S., J. Mater. Sci. 22 985 (1987).Google Scholar
[10] Hirano, S., Yogo, T., Kikuta, K. and Naka, S., J. Mater. Sci. 21 1951 (1986).Google Scholar
[11] Yogo, T., Tanaka, H., Naka, S. and Hirano, S., J. Mater. Sci. 25 1719 (1990).Google Scholar
[12] Yogo, T., Suzuki, H., Iwahara, H., Naka, S. and Hirano, S., J. Mater. Sci. 26 1363 (1991).Google Scholar
[13] Hirano, S., Yogo, T., Kikuta, K. and Fukuda, M., Ceram. Trans. 22 33 (1991).Google Scholar
[14] Hirano, S., Yogo, T., Kikuta, K., Takase, M. and Fukuda, M., Jpn. J. Chem. Soc., 1991 1261 (1991).Google Scholar