Doctoral Dissertations

Author

T. N. Tiegs

Date of Award

5-1997

Degree Type

Dissertation

Degree Name

Doctor of Philosophy

Major

Metallurgical Engineering

Major Professor

Thomas Meek

Committee Members

Carl McHargue, Pete Counce, Ray Buchanan, Peter Liaw

Abstract

Three inter-related aspects in the fabrication of silicon nitride ceramics were performed for the thesis work. The topics included: (1) an analysis of the composition and physical gradients in bulk silicon nitride, (2) the effect of sintering parameters on microstructure development during the high-temperature sintering stage and the resulting mechanical properties, and (3) an investigation of β-Si3N4 nucleation and initial stage microstructure development. The composition and physical gradients in bulk silicon nitride are due to the furnace conditions and the environment adjacent to the samples. Loss of SiO from the exposed surfaces results in the formation of nitrogen-rich phases, such as melilite on the as-sintered surfaces. The high nitrogen concentration in the near-surface region promotes β-Si3N4 grain growth. Along with the compositional gradients, mechanical property differences also exist between the as-sintered surfaces and the bulk materials. For example, the strengths of as-sintered surfaces of Si3N4-Y2O3-Al2O3 were observed to be reduced by more than 30% compared to the bulk material. Gas-pressure sintering (GPS) was used to densify silicon nitride containing a wide variety of sintering additives: Si3N4-6% Y2O3-2% Al2O3 and Si3N4-Sr2La4Yb4SiO4)6O4. For both compositions a lower densification temperature (1900°C in the present experiments) was the most significant factor affecting the fracture toughness and promoting a bimodal grain structure. The low significance of the other process parameters implies the microstructure (and therefore properties) are essentially 'locked-in' during the densification stage and only minor changes can take place afterward. Thus, the microstructural development that occurs during the densification dictates the final properties. The kinetics of the α-to-β Si4=3N4 transformation are dependent on several characteristics of the starting silicon nitride powder. Most importantly, are the silicon nitride powder surface area and initial β-Si3N4 content which both tend to increase the transformation rate. Other factors, such as lattice oxygen or carbon contents, appear to contribute to decreasing the transformation rate. In addition, the glass phase from the sintering additives also affects the transformation rate with higher viscosity and more refractory additives resulting in a decrease in the transformation rate. Larger volumes of the glass phase were observed to decrease the transformation rate.

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