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Effects of Rare‐Earth (RE) Intergranular Adsorption on the Phase Transformation, Microstructure Evolution, and Mechanical Properties in Silicon Nitride with RE 2 O 3 +MgO Additives: RE=La, Gd, and Lu
Author(s) -
Becher Paul F.,
Painter Gayle S.,
Shibata Naoya,
Waters Shirley B.,
Lin HuaTay
Publication year - 2008
Publication title -
journal of the american ceramic society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.9
H-Index - 196
eISSN - 1551-2916
pISSN - 0002-7820
DOI - 10.1111/j.1551-2916.2008.02448.x
Subject(s) - materials science , microstructure , phase (matter) , silicon nitride , adsorption , nitride , grain growth , lanthanide , silicon , chemical engineering , mineralogy , crystallography , metallurgy , nanotechnology , chemistry , ion , organic chemistry , layer (electronics) , engineering
Silicon nitride powders most often consist primarily of the α phase, which transforms into the β phase during the densification and microstructural evolution of Si 3 N 4 ceramics. The temperature at which the transformation initiates in the presence of a combination of MgO and RE 2 O 3 densification additives is found to decrease with increasing atomic number of the rare earth (RE). This trend coincides with the predicted and observed decrease in the affinity of the RE to segregate to and absorb on the prism planes of hexagonal prism‐shaped β grains with an increase in the atomic number of the RE. When RE adsorption is diminished, Si (and N) attachment on the smooth prism planes is enhanced, which increases diametrical growth rates, normally reaction‐rate limited by an attachment mechanism. Combined with the typically fast [0001] growth, it is this augmented grain growth that contributes toward the initiation of the α–β transformation at lower temperatures. With the enhanced transformation, observations reveal an increase in the number of β grains growing in the early stages of densification. On the other hand, increased RE adsorption leads to greater growth anisotropy, resulting in the formation of higher aspect ratio grains. Thus, Lu 2 O 3 generates larger diameter, yet elongated, reinforcing grains, while La 2 O 3 results in reinforcing grains of a higher aspect ratio. The Gd 2 O 3 additive transformation and microstructural characteristics lie intermediate to those of the lanthanide end‐member elements. Despite these differences, a substantial fraction of large reinforcing grains were found for each additive composition. As a result, the mechanical properties of the resultant ceramics are similar with flexure strengths in excess of 1 GPa, fracture toughness values >10 MPa·m 1/2 at room temperature, and excellent strength retention (>800 MPa) at 1200°C.