Preparation method for magnetic photocatalytic nano composite material
A nanocomposite material and photocatalysis technology, which is applied in the field of preparation of magnetic photocatalytic nanocomposite materials, can solve the problems of large energy gap and limited application, and achieve the effects of recycling, expanding the scope of application and reducing costs
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0020] (1) Add 1g FeCl 3 ·6H 2 O. 0.1g of sodium citrate and 1g of sodium acetate were added to the mixed solution of 50ml of ethylene glycol and 30ml of diethylene glycol, stirred at room temperature until dissolved, then the solution was transferred to an autoclave, and reacted for 10 hours at a temperature of 180°C to obtain black product. The black product was washed three times with deionized water and absolute ethanol respectively, and dried at 30° C. for 10 hours to finally obtain iron ferric oxide nanoparticles;
[0021] (2) Add 0.4g of iron ferric oxide nanoparticles obtained above, 0.2g of silver nitrate, and 4g of polyvinylpyrrolidone into 20ml of ethylene glycol solvent, stir and react at 100°C for 8 hours, and collect the product after the reaction is fully completed. The obtained product was washed three times with absolute ethanol and deionized water respectively, and dried at 40° C. for 12 hours to obtain ferric oxide / silver nanoparticles;
[0022] (3) Weigh...
Embodiment 2
[0025] (1) Add 1g FeCl 3 ·6H 2 O. 0.5g of sodium citrate and 3g of sodium acetate were added to a mixture of 60ml of ethylene glycol and 20ml of diethylene glycol, stirred at room temperature until dissolved, then the solution was transferred to an autoclave, and reacted at 200°C for 10 hours to obtain a black product. The black product was washed three times with deionized water and absolute ethanol respectively, and dried at 30° C. for 10 hours to finally obtain iron ferric oxide nanoparticles;
[0026] (2) Add 0.4g of iron ferric oxide nanoparticles obtained above, 0.2g of silver nitrate, and 4g of polyvinyl alcohol into 20ml of ethylene glycol solvent, and stir and react at 100°C for 8 hours. After the reaction is fully completed, the obtained product Wash with absolute ethanol and deionized water three times respectively, and dry at 40°C for 12 hours to obtain ferric oxide / silver nanoparticles;
[0027] (3) Weigh 0.4g of ferric oxide / silver nanoparticles obtained in ste...
Embodiment 3
[0030] (1) Add 1g FeCl 3 ·6H 2 O. 0.1g sodium citrate and 1g sodium acetate were added to a mixture of 50ml ethylene glycol and 30ml diethylene glycol, stirred at room temperature until dissolved, then the solution was transferred to an autoclave, and reacted at 220°C for 10 hours to obtain a black product. The black product was washed three times with deionized water and absolute ethanol respectively, and dried at 30° C. for 10 hours to finally obtain iron ferric oxide nanoparticles;
[0031] (2) Add 0.4g of iron ferric oxide nanoparticles obtained above, 0.2g of silver nitrate, and 4g of polyvinylpyrrolidone into 20ml of ethylene glycol solvent, and stir and react at 100°C for 8 hours. After the reaction is fully completed, the obtained product Wash with absolute ethanol and deionized water three times and dry at 40°C for 12 hours to obtain ferric oxide / silver nanoparticles;
[0032] (3) Weigh 0.2g of ferric oxide / silver nanoparticles obtained in step (2), and ultrasonical...
PUM
Property | Measurement | Unit |
---|---|---|
quality score | 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