Phase Transformation and Densification Behavior of Microwave Sintered γ-A12O3

1994 ◽  
Vol 347 ◽  
Author(s):  
John Freim ◽  
Joanna McKittrick ◽  
Joel Katz ◽  
Kurt Sickafus
Keyword(s):  
Phase Transformation ◽  
Phase Transformations ◽  
Growth Phase ◽  
Particle Morphology ◽  
Nucleation And Growth ◽  
Densification Behavior ◽  
Transformation Behavior ◽  
Gas Condensation ◽  
Grain Sizes ◽  
Dense Bodies

ABSTRACTThe phase transformation and densification behavior of gas condensation synthesized γA12O3 sintered with microwave radiation has been studied. Nucleation and growth phase transformations, which produce α-A12O3 occurred as the material was heated through the temperature range of 800–1300°C. These phase transformations resulted in anomalous grain growth with a distinct change in particle morphology, crystallite size and surface area. A12O3 derived from a chemically synthesized boehmite precursor has been shown to exhibit the same nucleation and growth phase transformation behavior when conventionally heated. It is concluded that nanocrystalline γ or β alumina will not be a viable starting material for the production of dense bodies with grain sizes of less than 100 nm.

Formation of Yttria Aluminium Garnet by Microwave Sintering

2020 ◽  
Vol 1010 ◽  
pp. 222-227 ◽  
Author(s):  
Ahmad Amirul Ashraf Abdul Halim ◽  
Izman Sudin ◽  
Wan Fahmin Faiz Wan Ali ◽  
Roslin Yasak ◽  
Rozlina Md. Sirat ◽  
...  
Keyword(s):  
Phase Transformation ◽  
Microwave Sintering ◽  
Xrd Analysis ◽  
Yttrium Aluminium Garnet ◽  
Densification Behavior ◽  
X Ray Diffraction ◽  
X Ray ◽  
Grain Sizes ◽  
Yttrium Aluminium ◽  
Three Phases

Polycrystalline yttrium aluminium garnet (YAG) ceramic has been prepared using microwave sintering. Micron-sized of Al2O3 and Y2O3 powders were mixed through in house fabrication mixer for 24 hours before calcined at 1100 °C and palletization process. The effect of sintering parameters on the microstructures was observed at various and holding times. X-ray diffraction (XRD) analysis was carried out to determine and quantify phase transformation with respect to these parameters. It was found that three phases namely YAM (Y4Al2O9), YAP (YAlO3) and YAG have been identified. While both grain sizes and density of sintered samples were found increased from 1.4 μm to 2.46 μm and 90% to 98%, respectively. Therefore, microwave sintering has a significant effect on the densification behavior of YAG.

Heat capacities and enthalpies of fusion and transformation for solvates of some salts with dimethyl sulfoxide and dimethylformamide

1988 ◽  
Vol 53 (12) ◽  
pp. 3072-3079
Author(s):  
Mojmír Skokánek ◽  
Ivo Sláma
Keyword(s):  
Heat Capacity ◽  
Phase Transformation ◽  
Phase Transformations ◽  
Dimethyl Sulfoxide ◽  
Liquidus Temperature ◽  
Molar Heat Capacity ◽  
Solid Phase ◽  
Zinc Nitrate ◽  
Heat Capacities ◽  
Liquid Phases

Molar heat capacities and molar enthalpies of fusion of the solvates Zn(NO3)2 . 2·24 DMSO, Zn(NO3)2 . 8·11 DMSO, Zn(NO3)2 . 6 DMSO, NaNO3 . 2·85 DMSO, and AgNO3 . DMF, where DMSO is dimethyl sulfoxide and DMF is dimethylformamide, have been determined over the temperature range 240 to 400 K. Endothermic peaks found for the zinc nitrate solvates below the liquidus temperature have been ascribed to solid phase transformations. The molar enthalpies of the solid phase transformations are close to 5 kJ mol-1 for all zinc nitrate solvates investigated. The dependence of the molar heat capacity on the temperature outside the phase transformation region can be described by a linear equation for both the solid and liquid phases.

Transformation behavior of yttria stabilized tetragonal zirconia polycrystal–TiB2 composites

2001 ◽  
Vol 16 (7) ◽  
pp. 2158-2169 ◽  
Author(s):  
B. Basu ◽  
J. Vleugels ◽  
O. Van Der Biest
Keyword(s):  
Thermal Expansion ◽  
Phase Transformation ◽  
Low Temperature ◽  
Tetragonal Zirconia ◽  
Mechanical Analysis ◽  
Transformation Behavior ◽  
Thermal Expansion Data ◽  
Thermally Induced ◽  
First Time ◽  
Tetragonal Zirconia Polycrystal

The objective of the present article is to study the influence of TiB2 addition on the transformation behavior of yttria stabilized tetragonal zirconia polycrystals (Y-TZP). A range of TZP(Y)–TiB2 composites with different zirconia starting powder grades and TiB2 phase contents (up to 50 vol%) were processed by the hot-pressing route. Thermal expansion data, as obtained by thermo-mechanical analysis were used to assess the ZrO2 phase transformation in the composites. The thermal expansion hysteresis of the transformable ceramics provides information concerning the transformation behavior in the temperature range of the martensitic transformation and the low-temperature degradation. Furthermore, the transformation behavior and susceptibility to low-temperature degradation during thermal cycling were characterized in terms of the overall amount and distribution of the yttria stabilizer, zirconia grain size, possible dissolution of TiB2 phase, and the amount of residual stress generated in the Y-TZP matrix due to the addition of titanium diboride particles. For the first time, it is demonstrated in the present work that the thermally induced phase transformation of tetragonal zirconia in the Y-TZP composites can be controlled by the intentional addition of the monoclinic zirconia particles into the 3Y-TZP matrix.

Enhanced crystallization and phase transformation of amorphous silicon nitride under high pressure

2001 ◽  
Vol 16 (1) ◽  
pp. 67-75 ◽  
Author(s):  
Ya-Li Li ◽  
Yong Liang ◽  
Fen Zheng ◽  
Xian-Feng Ma ◽  
Suo-Jing Cui ◽  
...  
Keyword(s):  
High Pressure ◽  
Phase Transformation ◽  
Silicon Nitride ◽  
Amorphous Silicon ◽  
Crystallization Temperature ◽  
Amorphous Materials ◽  
Normal Pressure ◽  
Nucleation And Growth ◽  
Amorphous Silicon Nitride ◽  
Amorphous Si

The crystallization and phase transformation of amorphous Si3N4 ceramics under high pressure (1.0–5.0 GPa) between 800 and 1700 °C were investigated. A greatly enhanced crystallization and α–β transformation of the amorphous Si3N4 ceramics were evident under the high pressure, as characterized by that, at 5.0 GPa, the amorphous Si3N4 began to crystallize at a temperature as low as 1000 °C (to transform to a modification). The subsequent a–b transformation occurred completed between 1350 and 1420 °C after only 20 min of pressing at 5.0 GPa. In contrast, under 0.1 MPa N2, the identical amorphous materials were stable up to 1400 °C without detectable crystallization, and only a small amount of a phase was detected at 1500 °C. The crystallization temperature and the a–b transformation temperatures are reduced by 200–350 °C compared to that at normal pressure. The enhanced phase transformations of the amorphous Si3N4 were discussed on the basis of thermodynamic and kinetic consideration of the effects of pressure on nucleation and growth.

Evolution of Phase Transformation Behavior in Li(Mn1.5Ni0.5)O4 Cathodes Studied By In Situ XRD

2011 ◽  
Vol 158 (8) ◽  
pp. A890 ◽  
Author(s):  
Kevin Rhodes ◽  
Roberta Meisner ◽  
Yoongu Kim ◽  
Nancy Dudney ◽  
Claus Daniel
Keyword(s):  
Phase Transformation ◽  
Transformation Behavior ◽  
Phase Transformation Behavior ◽  
In Situ Xrd
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