NIPPON KAGAKU KAISHI
Online ISSN : 2185-0925
Print ISSN : 0369-4577
Preparation of Various β″-Alumina Type Ferrites by Ion Exchange Method
Shinya NARIKIShigeru ITONoboru YONEDA
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1988 Volume 1988 Issue 2 Pages 131-138

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Abstract

The K+ ions in K+-β″-ferrite were exchanged with Nat, Rb+, Cs+, Ag+, T1+ and NH4+ions in the corresponding molten nitrates at 200--450°C or with H30+ ions in concentrated H2SO4 at 90°C, respectively, to form M+-β″-ferrites. The lattice constant co, which depends on the thickness of alkali layers, increased with increasing ionic radius of the ion inserted in the layers. In addition, the K+ ions in K+-β″-ferrite were found to be replaced by Ba2+ ions in Ba(NO3)2 melt at 650°C to form Ba2+-β″-ferrite. However, when the K+-β″-ferrite was immersed in a molten salt of other divalent cations (Mg2+, Co2+, Ca2+, Zn2+, Cd2+, Pb2+ or Sr2+ ion), the structure of K+-β″-ferrite was rearranged to form a s pinel ferrite, α-Fe2O3, γ-Fe2O3 or SrFe2O4.
The Rb+- and Cs+-β″-ferrites were partially decomposed to form α-Fe203 at about 800°C, and then were transformed to β phase at above 1050-1150°C. Ag+- and T1+-β″-ferrites were rapidly decomposed to form α-Fe203 at above 600°C. NH4+- and H30+-β″-ferrites were decomposed at the low temperature of 300°C to form γ-Fe2O3T as an intermediate phase, and this phase was transformed to α-Fe203 at 450°C. The formation of this intermediate phase may be due to the structural similarity of β″-ferrite to γ-Fe203.

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