Final-stage densification kinetics of direct current-sintered ZrB2

Final-stage sintering was analyzed for nominally phase pure zirconium diboride synthesized by borothermal reduction of high-purity ZrO2. Analysis was conducted on ZrB2 ceramics with relative densities greater than 90% using the Nabarro-Herring stress-directed vacancy diffusion model. Temperatures of 1900 degrees C or above and an applied uniaxial pressure of 50 MPa were required to fully densify ZrB2 ceramics by direct current sintering. Ram travel data were collected and used to determine the relative density of the specimens during sintering. Specimens sintered between 1900 and 2100 degrees C achieved relative densities greater than 97%, whereas specimens sintered below 1900 degrees C failed to reach the final stage of sintering. The average grain size ranged from 1.0 to 14.7 mu m. The activation energy was calculated from the slope of an Arrhenius plot that used the Kalish equation. The activation energy was 162 +/- 34 kJ/mol, which is consistent with the activation energy for dislocation movement in ZrB2. The diffusion coefficients for dislocation motion that controls densification were 5.1 x 10(-6) cm(2)/s at 1900 degrees C and 5.1 x 10(-5) cm(2)/s at 2100 degrees C, as calculated from activation energy and average grain sizes. This study provides evidence that the dominant mechanism for final-stage sintering of ZrB2 ceramics is dislocation motion.

Automated summary

The final-stage sintering process of zirconium diboride (ZrB2) ceramics was analyzed, and it was found that temperatures above 1900 degrees C and an applied uniaxial pressure of 50 MPa were necessary to achieve full density. Specimens sintered between 1900 and 2100 degrees C had relative densities greater than 97%, while those sintered below 1900 degrees C did not reach the final stage of sintering. The dominant mechanism for final-stage sintering was determined to be dislocation motion.