Preparation for soluble poly(3,4-ethylenedioxythiophene)
A ethylenedioxythiophene and soluble technology, which is applied in the field of preparation of soluble polyethylenedioxythiophene, can solve the problems of destroying the photoelectric properties of PEDOT, harsh synthesis conditions, and reducing the conjugated structure, so as to avoid corrosion problems and experimental conditions Low requirements for equipment and equipment, and the effect of increasing solubility
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0012] Add 0.62 g of DBSA to 25 ml of deionized water, stir at a speed of 60 r / min to completely disperse it, and prepare a solution with a molar concentration of 0.076 mol / L. 0.2 ml of monomeric EDOT was added to the above solution. The solution was cooled to 0° C. in an ice-water bath, and stirred at a speed of 30 r / min to prepare a monomer solution. Prepare 10ml of a deionized aqueous solution of ammonium persulfate with a molar concentration of 0.019mol / L, put it in an ice-water bath and cool it to 0°C, and then add the solution uniformly dropwise to the prepared monomer solution within 1 hour , the polymerization reaction was initiated to obtain polyoxyethylene thiophene, the reaction system was stirred in an ice-water bath at 0° C. at a speed of 30 r / min for 48 hours, and then 15 ml of acetone was added to break the emulsion and terminate the reaction. Then, the reaction product was separated by filtration under reduced pressure, and the reaction product was washed thre...
Embodiment 2
[0015] Add 2.48g of DBSA to 25ml of deionized water, and stir it at a speed of 60r / min to completely disperse it to form a solution with a molar concentration of 0.144mol / L. 0.2 ml of monomeric EDOT was added to the above solution. The solution was cooled to 0° C. in an ice-water bath, and stirred at a speed of 30 r / min to prepare a monomer solution. The concentration of the substance to prepare 10ml is 4.75×10 -3 mol / L deionized aqueous solution of ammonium persulfate, put it into an ice-water bath and cool it to 0°C, and then drop this solution evenly into the prepared monomer solution within 1 hour to initiate the polymerization reaction to obtain poly Ethylenedioxythiophene. The reaction system was stirred in an ice-water bath at 0° C. at a speed of 30 r / min for 48 hours, and then 15 ml of acetone was added to break the emulsion and terminate the reaction. Then the reaction product was separated by vacuum filtration, and the reaction product was repeatedly washed 3 time...
Embodiment 3
[0018] Add 0.15 g of DBSA to 25 ml of deionized water, stir at a speed of 40 r / min to completely disperse it, and prepare a solution with a molar concentration of 0.009 mol / L. 0.2 ml of monomeric EDOT was added to the above solution. The solution was cooled to 0° C. in an ice-water bath, and stirred at a speed of 30 r / min to obtain a monomer solution. Prepare 10ml of a deionized aqueous solution of ammonium persulfate with a substance concentration of 0.076mol / L, put it in an ice-water bath and cool it to 0°C, and then add the solution uniformly dropwise to the prepared monosulfate within 1 hour. In the body solution, the polymerization reaction was initiated to obtain polyethylenedioxythiophene. The reaction system was stirred in an ice-water bath at 0° C. at a speed of 30 r / min for 48 hours, and then 15 ml of acetone was added to break the emulsion and terminate the reaction. Then the reaction product was separated by vacuum filtration, and the reaction product was repeate...
PUM
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