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Cold sintering process for densification of Fe3O4 ceramic magnets with improved properties.

Authors :
Salidkul, Nuchjaree
Pinitsoontorn, Supree
Source :
Ceramics International. Apr2024:Part A, Vol. 50 Issue 7, p10873-10880. 8p.
Publication Year :
2024

Abstract

Iron oxide-based ferrite ceramics, widely applied in high-frequency applications, are conventionally produced through high-temperature sintering processes, often resulting in grain growth and phase transformation. In this study, we used a cold sintering process (CSP) with oxalic acid (OA) as a solvent to consolidate iron oxide (Fe 3 O 4) ceramics at a low temperature of 160 °C. The OA-assisted CSP technique has demonstrated a remarkable capacity to facilitate the dissolution and redeposition of iron oxide ions, leading to the interconnection of Fe 3 O 4 particles, forming densely packed ceramics even at low-temperature sintering. Importantly, CSP maintained particle sizes and hindered phase transitions of Fe 3 O 4. The OA concentrations in CSP had a minimal impact on crystal structure and magnetic properties, but it significantly enhanced microstructural features, density, hardness, and electrical resistance. Compared to reference samples prepared without an aqueous solution or with water alone, the CSP-prepared Fe 3 O 4 ceramics with OA exhibited substantially improved density (a relative density of ∼80 %), mechanical properties (Vickers hardness of 3.5–4.0 GPa), magnetic properties (saturation magnetization >70 emu/g), and electrical resistance (electrical conductivity ∼10−3 S/cm at 102–106 Hz). These findings demonstrate a novel approach to fabricating Fe 3 O 4 ceramics at significantly lower temperatures while still achieving properties comparable to those sintered at high temperatures. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
02728842
Volume :
50
Issue :
7
Database :
Academic Search Index
Journal :
Ceramics International
Publication Type :
Academic Journal
Accession number :
175643949
Full Text :
https://doi.org/10.1016/j.ceramint.2023.12.403