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Kinetics and mechanism of high-temperature oxidation of the heterophase ZrSi2-MoSi2-ZrB2 ceramics
- Source :
- Ceramics International. 45:6392-6404
- Publication Year :
- 2019
- Publisher :
- Elsevier BV, 2019.
-
Abstract
- The kinetics and mechanism of high-temperature oxidation of dense heterophase ZrSi2-MoSi2-ZrB2 ceramics at a temperature of 1650 °C are studied. The ceramics were fabricated by hot pressing of composite powders prepared by self-propagating high-temperature synthesis with magnesiothermic reduction. The oxidation kinetic curve is described by the power-law function, which indicates that the evolutionary changes in the structure of the formed oxide films significantly affect the course of the oxidation process. The oxidation mechanism involves formation of a multi-layered structure of heterogeneous oxide film, partial dissociation of the ZrSiO4 phase, and formation of secondary MoB and Mo5Si3 compounds. The influence of the ZrSi2, MoSi2 and ZrB2 phases on the structural and morphological features of the formed oxide films and the efficiency of their protective action are shown. Silicon is reduced and zirconium is simultaneously oxidized to ZrO2 in the ZrSi2-ZrSiO4 system at temperatures above 1620 °C in the absence of oxygen or in low-oxygen environment.
- Subjects :
- 010302 applied physics
Zirconium
Materials science
Silicon
Process Chemistry and Technology
Composite number
Kinetics
Oxide
chemistry.chemical_element
02 engineering and technology
021001 nanoscience & nanotechnology
Hot pressing
01 natural sciences
Oxygen
Dissociation (chemistry)
Surfaces, Coatings and Films
Electronic, Optical and Magnetic Materials
chemistry.chemical_compound
chemistry
Chemical engineering
0103 physical sciences
Materials Chemistry
Ceramics and Composites
0210 nano-technology
Subjects
Details
- ISSN :
- 02728842
- Volume :
- 45
- Database :
- OpenAIRE
- Journal :
- Ceramics International
- Accession number :
- edsair.doi...........c4d643d17ebcbe428db96c239ab6d892
- Full Text :
- https://doi.org/10.1016/j.ceramint.2018.12.126