Process of preparing zirconia and yttria with Y-doped cubic zirconia powder
A phase zirconia, powder-based technology, applied in the field of preparation of zirconium and yttrium oxides, can solve the problems of mutual interference between zirconium and yttrium, and the troublesome determination of hafnium in zirconium.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0059] Mix 1Kg yttrium-zirconium powder with 0.8Kg caustic soda and 0.1Kg borax and fuse in an iron crucible at 350°C for 30 minutes, take out the melt and cool it to 150°C, put it in a magnesium refractory sagger and react in a high-temperature furnace at 800°C After 1 hour, 1.8Kg of sintered material was obtained. The sintered material was crushed to below 150 mesh. The liquid-solid ratio was 5 and water was added for leaching for 25 minutes. The soft water was washed twice with a liquid-solid ratio of 3, and the precipitate was soaked with 2 liters of hydrochloric acid with a concentration of 1mol / L. 30 minutes, rinse with 0.4mol / L hydrochloric acid to Na:Zr≤1:80, and the hydrochloric acid of 25% by weight reacts with it, and reaction temperature is 95 ℃, acidity 2.5mol / L, concentrates to Baume degree B'= 32°, add concentrated hydrochloric acid to control the acidity at 5.5mol / L, cool and crystallize, rinse with 6mol / L hydrochloric acid with a liquid-solid ratio of 10 to obt...
Embodiment 2
[0064] Mix 45Kg of yttrium-zirconium powder with 35Kg of caustic soda and 5Kg of borax and fuse them in an iron crucible at 400°C for 50 minutes, take out the melt and cool it to 150°C, put it into a simple reverberatory furnace at 900°C for 1.5 hours to obtain a sintered material 84.5Kg, pulverize below 150 mesh, add water for leaching for 1 hour with a liquid-solid ratio of 5, wash twice with soft water with a liquid-solid ratio of 4, filter out and soak the precipitate with 1mol / L hydrochloric acid with a liquid-solid ratio of 3:2 for 50 minutes, and use 0.6mol / L L hydrochloric acid rinse to Na:Zr≤1:80, 30% by weight hydrochloric acid reacts with it, reaction temperature 105°C, acidity 3.0mol / L, concentrate to Baume degree B'=34°, add concentrated hydrochloric acid to control acidity At 6.0mol / L, cooling and crystallization, 6.5mol / L hydrochloric acid with a liquid-solid ratio of 10 was rinsed to obtain zirconium oxychloride crystals and yttrium-rich mother liquor, and the z...
Embodiment 3
[0070] Mix 1.05Kg yttrium-zirconium powder with 0.7Kg caustic soda and 0.08Kg borax and fuse in an iron crucible at 400°C for 45 minutes, take out the melt and cool it to 150°C, put it in a magnesium refractory sagger and place it in a high-temperature furnace at 850°C React for 1.2 hours to obtain 1.7Kg of sintered material, crush it below 150 mesh, add water to leaching for 30 minutes at a liquid-solid ratio of 5, wash twice with soft water at a liquid-solid ratio of 4, filter out and soak the precipitate with 2 liters of hydrochloric acid with a concentration of 1mol / L for 40 minutes , rinsed with 0.7mol / L hydrochloric acid until Na:Zr≤1:80, 28% by weight of hydrochloric acid reacted with it, the reaction temperature was 100°C, the acidity was 2.7mol / L, concentrated to Baume degree B'=33°, Add concentrated hydrochloric acid to control the acidity at 5.8mol / L, cool to room temperature to crystallize, rinse with 6.2mol / L hydrochloric acid with a liquid-solid ratio of 10 to obt...
PUM
Property | Measurement | Unit |
---|---|---|
density | aaaaa | aaaaa |
density | aaaaa | aaaaa |
density | aaaaa | aaaaa |
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com