Method for preparing polyaniline derivative-metal complex
A technology for metal complexes and aniline, which is applied in the field of preparation of polyaniline derivatives-metal complexes, can solve the problems of cumbersome preparation process, insufficient environmental protection and high operation cost, and achieves the effect of simple and easy method.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0020] Add 1.20 g of 5-[(anilino)methyl]-8-hydroxyquinoline and 15.9 g of aluminum sulfate into 38 ml of 1 mol / L sulfuric acid aqueous solution, and ultrasonically disperse for 20 minutes. Under the condition of continuous stirring, acidic aqueous solution containing ammonium persulfate (1.09g ammonium persulfate dissolved in 10ml 1mol / L sulfuric acid solution) was gradually added dropwise, the reaction time was controlled at 48 hours, and the reaction temperature was 25°C. After the reaction, the product was suction filtered with a Buchner funnel, washed with deionized water until the filtrate was neutral, and finally dried in a vacuum oven at 60°C to obtain dark green poly N-[5-(-8-hydroxyquinone Phenyl) methyl] aniline-aluminum complex powder. FTIR (KBr) shows that the main characteristic absorption peak (1000cm -1 ~1800cm -1 between) is similar to conductive polyaniline. Thanks Al 3+ Coordination with the phenolic hydroxyl group on the quinoline ring results in a 3200c...
Embodiment 2
[0022] Add 1.20 g of 5-[(anilino)methyl]-8-hydroxyquinoline and 15.9 g of aluminum sulfate into 38 ml of 1.5 mol / L sulfuric acid aqueous solution, and disperse by ultrasonic for 15 minutes. Under the condition of continuous stirring, gradually add dropwise the acidic aqueous solution containing ammonium persulfate (0.55g ammonium persulfate is dissolved in the sulfuric acid solution of 10ml 1.5mol / L), the dropping time is controlled at 10 minutes, and the reaction time is controlled at 56 hours , and the reaction temperature was 5°C. After the reaction, the product was suction filtered with a Buchner funnel, washed with deionized water until the filtrate was neutral, and finally dried in a vacuum oven at 50°C to obtain dark green poly N-[5-(-8-hydroxyquinone Phenyl) methyl] aniline-aluminum complex powder.
[0023] FTIR (KBr) shows that the main characteristic absorption peak (1000cm -1 ~1800cm -1 between) is similar to conductive polyaniline. Thanks Al 3+ Coordination wi...
Embodiment 3
[0025] Add 1.20g of 5-[(anilino)methyl]-8-hydroxyquinoline and 6.40g of aluminum sulfate into 38ml of 1mol / L sulfuric acid solution, and disperse by ultrasonic for 5 minutes. Under continuous stirring condition, gradually add dropwise the acidic aqueous solution (1.09g ammonium persulfate is dissolved in the sulfuric acid solution of 10ml 1mol / L) that contains ammonium persulfate, the time of dropping is controlled at 30 minutes, and the reaction time is controlled at 42 hours, the reaction The temperature is 20°C. After the reaction, the product was suction filtered with a Buchner funnel, washed with deionized water until the filtrate was neutral, and finally dried in a vacuum oven at 60°C to obtain dark green poly N-[5-(-8-hydroxyquinone Phenyl) methyl] aniline-aluminum complex powder.
[0026] FTIR (KBr) shows that the main characteristic absorption peak (1000cm -1 ~1800cm -1 between) is similar to conductive polyaniline. Thanks Al 3+ Coordination with the phenolic hyd...
PUM
Property | Measurement | Unit |
---|---|---|
Conductivity | aaaaa | aaaaa |
Conductivity | aaaaa | aaaaa |
Conductivity | 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