Method for preparing tin-doped indium oxide nano powder
A tin-doped indium oxide and nano-powder technology, which is applied in chemical instruments and methods, tin compounds, inorganic chemistry, etc., can solve the problems of reducing powder dispersion performance, reducing the service life of components, and corrosion in the use environment, so as to eliminate Removal of problems, less agglomeration, good dispersion effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
preparation example Construction
[0012] The preparation method of said tin-doped indium oxide nanopowder in the present invention comprises the following steps:
[0013] (1) Dissolve the water-soluble tin-containing compound and the water-soluble indium-containing compound in deionized water at 20-90°C under stirring conditions, so that the concentration of indium ions in the solution is 0.01-5mol / L (tin ions and indium ions The molar ratio is 3~15:100);
[0014] (2) carry out precipitation reaction at 30~90 ℃ with the aqueous solution containing tin ion and indium ion obtained by step (1) and the ammoniacal liquor with concentration of 1~12mol / L, the feeding method of precipitation reaction: can be to contain indium and tin The aqueous solution of ions is added dropwise to the ammonia solution, or the aqueous solution containing indium and tin ions and ammonia water are added dropwise to deionized water, or the ammonia water is added dropwise to the aqueous solution containing indium and tin ions;
[0015] ...
Embodiment 1
[0018] Under the condition of 20°C, 10g of indium sulfate and the molar ratio of tin and indium are 3:100, weigh stannous oxalate and dissolve it in deionized water, and prepare the concentration of indium ion as 0.1molL -1 The mixed solution, under vigorous stirring, with 1molL -1 The ammonia water used as a precipitant was slowly added dropwise to the above mixed solution, and the reaction temperature was controlled at 60°C. When the pH value of the system reached 8, the dropwise addition was stopped, and the reaction was stirred for 2 to 10 hours to obtain a pale yellow colloidal precipitation precursor. . The precursor was washed with deionized water and absolute ethanol. The obtained product was dried at 90° C. for 3 hours. Finally, heat-treat the dried powder at 800°C for 6 hours, and the obtained light yellow powder is ITO nano powder. The powder is detected by the X-ray diffraction method, and the (222) crystal plane of the powder is calculated by the Scherrer formu...
Embodiment 2
[0020] Under the condition of 90°C, weigh 25g of indium oxalate and the molar ratio of tin to indium is 8:100, take tin nitrate and dissolve it in deionized water, and prepare the indium ion concentration as 0.01molL -1 The mixed solution, under vigorous stirring, 12molL -1 The ammonia water and the above mixed solution are added dropwise to strongly stirred deionized water at a temperature of 70°C for co-precipitation reaction. The pH value of the system is always controlled at about 5, and the reaction is stirred for 2 to 10 hours to obtain a light yellow gel Precipitate the precursor. The precursor was washed with deionized water and absolute ethanol. The obtained product was dried at 120° C. for 2 hours. Finally, heat-treat the dried powder at 600°C for 4 hours, and the obtained light yellow powder is ITO nano powder. The powder is detected by the X-ray diffraction method, and the (222) crystal plane of the powder is calculated by the Scherrer formula to obtain a grain ...
PUM
Property | Measurement | Unit |
---|---|---|
particle diameter | 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