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Phase formation and composition of Mn–Zn ferrite powders prepared by hydrothermal method

Published online by Cambridge University Press:  26 July 2012

Wen-Hao Lin
Affiliation:
Department of Materials Science and Engineering, National Cheng Kung University, Tainan, Taiwan, Republic of China
Shiuh-Ke Jang Jean
Affiliation:
Department of Materials Science and Engineering, National Cheng Kung University, Tainan, Taiwan, Republic of China
Chii-Shyang Hwang
Affiliation:
Department of Materials Science and Engineering, National Cheng Kung University, Tainan, Taiwan, Republic of China
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Extract

Mn–Zn ferrite powders were prepared by hydrothermally aging the coprecipitates of compositional metal ions using ammonium hydroxide as a precipitant. R value (alkalinity) = (moles of added OH)/[(moles of added Zn2+) × 2 + (moles of added Mn2+) × 2 + (moles of added Fe3+) × 3] was introduced to adjust the amount of added ammonia. The results show that the R value of starting suspension and hydrothermal time have similar and dominant effects on the composition, spinel ratio, and crystallite size of synthesized powders. From the analyses of x-ray diffraction (XRD) and inductively-coupled plasma (ICP), it notes that no α–Fe2O3 peak in the XRD patterns of powders synthesized at R = 2–3, 150 °C × 2 h, may be due to lower degree of crystallinity and less amount of α–Fe2O3 existing in these powders. Both the increase of hydrothermal time and of R value can promote the crystallinity of powders and also cause a significant loss of zinc, hinting that in the hydrothermal process, the loss of zinc may play a crucial role in the crystallinity of hydrothermally synthesized powders.

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Articles
Copyright
Copyright © Materials Research Society 1999

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References

REFERENCES

1.Taylor, J. A. T., Reczek, S. T., and Rosen, A., Am. Ceram. Soc. Bull. 74 (4), 9194 (1995).Google Scholar
2.Kim, K.Y., Kim, W. S., Ju, Y.D., and Jung, H.J., J. Mater. Sci. 27 (17), 47414745 (1992).CrossRefGoogle Scholar
3.Fujimoto, M., J. Am. Ceram. Soc. 77 (11), 28732878 (1994).CrossRefGoogle Scholar
4.Yu, B.F. B. and Goldman, A., in Ferrites, Proc. ICF, 3rd. ed., Japan, edited by Watanabe, H., Iida, S., and Sugimoto, M. (Center for Academic Press, Tokyo, Japan, 1982), p. 68.CrossRefGoogle Scholar
5.Yu, B.F. B. and Goldman, , U.S. Patent 4,372,865A (1983).Google Scholar
6.Beer, H.B., Van den Keybus, F. A.M, and Suykerbuyk, L.F., PCT International Patent (US), WO 8,301,464 A1 (1983).Google Scholar
7.Aoyama, T., Hirota, K., and Yamaguchi, O., J. Am. Ceram. Soc. 79 (10), 27922794 (1996).CrossRefGoogle Scholar
8.Komarneni, S., Fragean, E., Brevel, E., and Roy, R., J. Am. Ceram. Soc. 7 (1), C-26C-27 (1988).Google Scholar
9.Rozman, M. and Drodenik, M., J. Am. Ceram. Soc. 78 (9), 24492455 (1995).CrossRefGoogle Scholar
10.Dawson, W.J., Am. Ceram. Soc. Bull. 67 (19), 16731678 (1988).Google Scholar
11.Komarneni, S., Roy, R., Brevel, E., Ollinen, M., and Sawa, Y., Adv. Ceram. Mater. 1 (1), 8792 (1986).Google Scholar
12.Chang, C.W., Hong, Y. S., Wang, S.J., and Lin, I.N., Chinese J. Mater. Soc. 23 (1), 6271 (1991).Google Scholar
13.Schikorr, G., Z. Anorg. Allg. Chem. 212, 3338 (1933).CrossRefGoogle Scholar
14.Autissier, D. and Autissier, L., Proceedings of ICF6, Tokyo, Japan (1992), pp. 132135.Google Scholar
15.Klug, H.P. and Alexander, L. E., X-ray Diffraction Procedures (John Wiley, New York, 1974), Chap. 9.Google Scholar