Method for preparing ITO powder with high sintering activity
A sintering activity, powder technology, applied in chemical instruments and methods, inorganic chemistry, gallium/indium/thallium compounds, etc., can solve the problems of corrosion in the use environment and reducing the service life of components
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0010] The method for preparing ITO powder with high sintering activity of the present invention includes the following steps:
[0011] (1) First, dissolve the tin source and indium source without chloride ions into deionized water at 0~90℃ and stirring conditions to prepare the indium ion concentration to be 0.1~3mol / L, the molar ratio of tin ion and indium ion A solution with a ratio of (3~12):100; then add organic complexing agent to the solution, the molar ratio of organic complexing agent to metal ion (the sum of tin ion and indium ion) is (0.25~5):1 ; Finally, add ammonia water to adjust the pH to 4-12;
[0012] (2) Put the mixture containing indium, tin and organic complexing agent in a reactor with a pH value of 4-12 prepared in step (1), and conduct a hydrothermal reaction at 130-260°C for 3-24 hours. The thermal reaction product is washed with deionized water and absolute ethanol and dried at 80-130°C for 1 to 5 hours, and the dried hydrothermal reaction product is heat-...
Embodiment 1
[0019] Accurately weigh 15g of indium isopropoxide, weigh out stannous nitrate according to the molar ratio of tin to indium of 10:100, and prepare it to 3molL -1 The mixed solution, the preparation temperature is 0 ℃. Under vigorous stirring, triethylamine was added to the above solution, the molar ratio of triethylamine to metal ions (the sum of tin ions and indium ions) was 1:1, and the pH value of the system was adjusted to 12 with ammonia water. The system was transferred to an autoclave for hydrothermal reaction, the hydrothermal temperature was 160°C, and the hydrothermal time was 7 hours. After the hydrothermal reaction, the hydrothermal product was taken out, washed several times with deionized water and absolute ethanol, and then dried at 130°C for 3 hours. The dried hydrothermal powder is heat-treated at 700°C for 2 hours to obtain the product ITO powder. The powder was measured by X-ray diffraction method, and the crystal plane at 31.0° in the powder diffraction peak w...
Embodiment 2
[0022] Accurately weigh 10g of indium citrate, weigh tin iodide according to the molar ratio of tin to indium of 3∶100, and prepare 1molL -1 The mixed solution is prepared at a temperature of 40°C. Under vigorous stirring, tartaric acid is added to the above solution, the molar ratio of tartaric acid to metal ions (the sum of tin ions and indium ions) is 0.25:1, and the pH value of the system is adjusted to 6 with ammonia water. The system was transferred to an autoclave for hydrothermal reaction, the hydrothermal temperature was 260°C, and the hydrothermal time was 3 hours. After the hydrothermal reaction, the hydrothermal product was taken out, washed several times with deionized water and absolute ethanol, and then dried at 80°C for 2 hours. The dried hydrothermal powder is heat treated at 900°C for 5 hours to obtain the product ITO powder. The powder was measured by X-ray diffraction method, and the crystal plane at 31.0° in the powder diffraction peak was calculated with Sche...
PUM
Property | Measurement | Unit |
---|---|---|
particle size | aaaaa | aaaaa |
particle size | aaaaa | aaaaa |
particle size | 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