Method for preparing nano barium strontium titanate powder by adopting sol-gel method
A technology of nano-titanium and gel method, which is applied in the direction of nanotechnology, nanotechnology, nanostructure manufacturing, etc., can solve the problem of uneven particle size distribution of barium strontium titanate powder, and achieve the effect of uniform particle size distribution
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0014] Example 1, 1 mol of strontium hydroxide was added to 300 ml of glacial acetic acid, heated and dissolved in a water bath at 80° C. with stirring. After the solution turns into a clear solution, add 1.5 mol of barium acetate. Then add 600ml ethylene glycol methyl ether solution as a solvent, and stir for 10min. 7.5 mol of tetra-n-butyl titanate was weighed and added dropwise to the solution, and after stirring for half an hour, 150 ml of acetylacetone was slowly added. Then heated and stirred at 80° C. for 3 h. Finally, 50ml of deionized water was added. The amount of deionized water added was preferably such that the color of the solution turned into an orange sol. Stir and heat at the same temperature to obtain a BST gel. The obtained BST gel was dried at 120°C, ground and sieved, and then heat-treated at 750°C for 5 hours at a heating rate of 1°C / min to synthesize a pure-phase BST nanopowder.
[0015] The surface morphology and phase of the prepared BST nanopowder ...
Embodiment 2
[0019] Example 2, 2 mol of strontium hydroxide was added to 400 ml of glacial acetic acid, heated and dissolved in a 60° C. water bath with stirring. After the solution turns into a clear solution, add 3 mol of barium acetate. Then add 800ml ethylene glycol methyl ether solution as a solvent, and stir for 15min. Weigh 15 mol of tetra-n-butyl titanate and add it dropwise into the solution, and after stirring for 20 min, slowly add 200 ml of acetylacetone. Then heated and stirred at 70°C for 4h. Finally, 50ml of deionized water was added. The amount of deionized water added was preferably such that the color of the solution turned into an orange sol. Stir and heat at the same temperature to obtain a BST gel. The obtained BST gel was dried at 115°C, ground and sieved, and then heat-treated at 800°C for 4 hours at a heating rate of 4°C / min to synthesize a pure-phase BST nanopowder. The surface morphology and phase of the samples were analyzed and characterized by Hitach S-530 s...
Embodiment 3
[0023] Example 3, 3 mol of strontium hydroxide was added to 500 ml of glacial acetic acid, heated and dissolved in a 70° C. water bath with stirring. After the solution turns into a clear solution, add 4.5 mol of barium acetate. Then add 1000ml ethylene glycol methyl ether solution as a solvent, and stir for 8min. Weigh 22.5 mol of tetra-n-butyl titanate and add it dropwise into the solution. After stirring for 15 min, slowly add 250 ml of acetylacetone. Then heated and stirred at 90 °C for 1 h. Finally, 50ml of deionized water was added. The amount of deionized water added was preferably such that the color of the solution turned into an orange sol. Stir and heat at the same temperature to obtain a BST gel. The obtained BST gel was dried at 110°C, ground and sieved, and then heat-treated at 850°C for 3 hours at a heating rate of 3°C / min to synthesize a pure-phase BST nanopowder. The surface morphology and phase of the samples were analyzed and characterized by Hitach S-530...
PUM
Property | Measurement | Unit |
---|---|---|
Scale | aaaaa | aaaaa |
Scale | 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