Coercivity and superparamagnetic evolution of high energy ball milled (HEBM) bulk CoFe2O4 material
- 1. Department of Physics, University of Puerto Rico-Mayagueez, P. O. Box 9016 Mayagueez, 00681-9016 (Puerto Rico)
- 2. Department of Mechanical Engineering, University of Puerto Rico-Mayagueez, P. O. Box 9045 Mayagueez, 00681-9045 (Puerto Rico)
- 3. Department of Engineering Science and Materials, University of Puerto Rico-Mayagueez, P. O. Box 9044 Mayagueez, 00681-9044 (Puerto Rico)
Description
Ball milling (BM) of bulk CoFe2O4 powder material carried out in order to study its structural stability and attendant property changes with respect to coercivity enhancements and superparamagnetic behaviors, showed that drastic crystallite size reduction occurred within the first 1 h of ball milling. Crystallite size dropped from 74 nm for the as-received material to a value of 11.6 nm for 600 min of ball milling. Combined X-ray diffraction (XRD) and scanning electron microscopy (SEM) analyses confirmed crystallite size reduction with corresponding increase in interparticle agglomeration/pores with increasing milling time. The maximum coercivity of 0.46 T and the crystallite size of 15.6 nm were recorded with 20 min, while peak residual strain of 0.0066 mm/mm was for 180 min of BM. Material with peak coercivity value did not have peak residual strain, or minimum crystallite size, thereby suggesting that other structural defects contributed to coercivity enhancement. The saturation magnetization (Ms) value decreased continuously with increasing milling time, while remanence magnetization (Mr) and coercivity decreased with increasing BM time, after an initial increase. Moessbauer spectroscopy (MS) measurements confirmed both particle size distribution and decomposition/disordering of the material together with superparamagnetism as BM time increased. The degree of inversion ranged from 41% to 71.7% at different milled states from Moessbauer spectroscopy. The internal magnetic fields of the Fe sites associated with the tetrahedral and octahedral sites were 507.4 kOe and 492 kOe respectively in the unmilled state, while 484 kOe and 468.5 kOe in the 600 min milled state correspondingly.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.matchar.2010.04.013Additional details
Identifiers
- DOI
- 10.1016/j.matchar.2010.04.013;
- PII
- S1044-5803(10)00119-1;
Publishing Information
- Journal Title
- Materials Characterization
- Journal Volume
- 61
- Journal Issue
- 12
- Journal Page Range
- p. 1317-1325
- ISSN
- 1044-5803
- CODEN
- MACHEX
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 44022858
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- ABSORPTION SPECTROSCOPY; COBALT COMPOUNDS; COERCIVE FORCE; DECOMPOSITION; FERRITES; MAGNETIC FIELDS; MAGNETIZATION; MILLING; MOESSBAUER EFFECT; PARTICLE SIZE; PHASE STABILITY; POWDERS; SCANNING ELECTRON MICROSCOPY; STRAINS; SUPERPARAMAGNETISM; X-RAY DIFFRACTION
- Descriptors DEC
- CHEMICAL REACTIONS; COHERENT SCATTERING; DIFFRACTION; ELECTRON MICROSCOPY; FERRIMAGNETIC MATERIALS; IRON COMPOUNDS; MACHINING; MAGNETIC MATERIALS; MAGNETISM; MATERIALS; MICROSCOPY; OXYGEN COMPOUNDS; SCATTERING; SIZE; SPECTROSCOPY; STABILITY; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Copyright
- Copyright (c) 2010 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.