Activation volume and coercivity in aluminum-substituted Pb-M hexaferrites
Description
PbFe12-xAlxO19 samples were obtained by the chemical coprecipitation method with compositions x=0.0, 3.0, 4.0, 6.0. As was expected, significant differences in magnetization reversal mechanisms were found at room temperature in these specimens. A magnetic viscosity study was carried out in the temperature range of 75-300 K in order to obtain information related to the mechanism of magnetization behavior. A logarithmic time dependence of the magnetization was observed during a period of 20-1200 s. The magnetic viscosity Sv and the activation volume Va increase as temperature is increased; the samples x=3.0 and 4.0 show the most rapid increase of the activation volume with temperature. Except for the samplesx=3.0 and 4.0, the experimental temperature dependencies of the coercive field are in agreement with a model due to Givord and co-workers in which the magnetization reversal occurs in a volume equal to the activation volume
Additional details
Identifiers
- PII
- S0304885300004315;
Publishing Information
- Journal Title
- Journal of Magnetism and Magnetic Materials
- Journal Volume
- 222
- Journal Issue
- 3
- Journal Page Range
- p. 271-276
- ISSN
- 0304-8853
- CODEN
- JMMMDC
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 34036888
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- ALUMINIUM ALLOYS; COERCIVE FORCE; COPRECIPITATION; FERRITES; INTERMETALLIC COMPOUNDS; IRON ALLOYS; LEAD ALLOYS; MAGNETIC FIELD REVERSAL; MAGNETIZATION; TEMPERATURE DEPENDENCE; TEMPERATURE RANGE 0065-0273 K; TEMPERATURE RANGE 0273-0400 K; TIME DEPENDENCE
- Descriptors DEC
- ALLOYS; FERRIMAGNETIC MATERIALS; IRON COMPOUNDS; MAGNETIC FIELD CONFIGURATIONS; MAGNETIC MATERIALS; MATERIALS; OXYGEN COMPOUNDS; PRECIPITATION; SEPARATION PROCESSES; TEMPERATURE RANGE; TRANSITION ELEMENT ALLOYS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2000 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.