Magnetic properties of cobalt substituted M-type barium hexaferrite prepared by co-precipitation
The co-precipitation and solid state methods were used in the synthesis of barium hexaferrite (BaM). Phase pure BaM was obtained with 1, 2, 3, 5, 10, 15, 20 and 30 wt% cobalt oxide (Co 3O 4). The addition of Co 2+/3+ ions to the BaM increased the permeability and magnetic loss tangent to a value of...
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Published in: | Journal of magnetism and magnetic materials Vol. 312; no. 2; pp. 418 - 429 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
Amsterdam
Elsevier B.V
01-05-2007
Elsevier Science |
Subjects: | |
Online Access: | Get full text |
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Summary: | The co-precipitation and solid state methods were used in the synthesis of barium hexaferrite (BaM). Phase pure BaM was obtained with 1, 2, 3, 5, 10, 15, 20 and 30
wt% cobalt oxide (Co
3O
4). The addition of Co
2+/3+ ions to the BaM increased the permeability and magnetic loss tangent to a value of 3.5 at 5% and reduced to 1 at 30% doping. With increased Co doping,
M
s was reduced from 87-58
emu/g,
M
r increased from 11 to 40
emu/g with 3–5
wt% Co and 9
emu/g for 30% doping.
H
c sharply increased from 540 to 2200
Oe with a reduction to 280
Oe at 10
K with increasing temperature to 300
K.
T
c increased from 740 to 750
K for 30% Co doping. DTA–TGA studies of green body showed decarboxilation to occur at around 825
°C and the transformation of residual Co
3O
4 to Co
2O
3 at around 577
°C. The XRD data confirmed the Co ions substituting into Fe sites until a 10–15% doping level where the structure altered to W-type hexaferrite. The densities of the compounds varied with doping to a maximum of 4.45 g/cm
3. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0304-8853 |
DOI: | 10.1016/j.jmmm.2006.11.130 |