Microstructural and spectroscopic analysis in non-uniform Y2O3 ceramics fabricated by spark plasma sintering
In Y2O3 ceramics densified at 1000 °C by spark plasma sintering (SPS), non-uniform sintering behavior of grains and pores occurred for a heating rate of 20 °C/min. The sintered Y2O3 was translucent at the periphery but white and opaque at the center. According to microstructural analysis, the non-un...
Gespeichert in:
Veröffentlicht in: | Journal of the Ceramic Society of Japan 2021/01/01, Vol.129(1), pp.66-72 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | In Y2O3 ceramics densified at 1000 °C by spark plasma sintering (SPS), non-uniform sintering behavior of grains and pores occurred for a heating rate of 20 °C/min. The sintered Y2O3 was translucent at the periphery but white and opaque at the center. According to microstructural analysis, the non-uniform sintering was caused by rapid grain growth and pore coarsening at the center. Under complicated electric and magnetic fields during SPS, an assumption of the movement of defects toward the center enables to explain the microstructural non-uniformity. For the non-uniform sintering behavior, spectroscopic analysis was used to investigate the introduced impurities (C, H, O) and by-products (carbonates). In the spectroscopic analysis, the peaks located at 2555, 2950, and 3560 cm−1 (O–H stretching band of H2O) were weakly detected for low heating rates but clearly detected for high heating rates. This is because H2O adsorbed to the initial Y2O3 powder was not sufficiently removed and was trapped during rapid densification at high heating rates. Due to the carbon-rich environment during SPS, carbonate was formed by the reaction of carbon with –OH. Most carbons were detected as a C–O peak, indicating that a reaction of carbon with –OH occurred. |
---|---|
ISSN: | 1882-0743 1348-6535 |
DOI: | 10.2109/jcersj2.20173 |