Poly(2-hydroxyethyl methacrylate) and anion exchange membrane for vanadium battery
A poly(hydroxyethyl methacrylate) and vanadium battery technology, which is applied in the field of electrochemical materials, can solve the problems of complex process, high production cost, and high moisture content, and achieve easy environmental friendliness, low cost, and easy industrial production Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0048] A synthetic method for polyhydroxyethyl methacrylate, comprising the following steps:
[0049] (1) In a round-bottomed flask, add 1mmol 4-bromomethylbenzophenone, 50mmol hydroxyethyl methacrylate, 1mmol cuprous bromide, 1mmol pentamethyldiethylenetriamine and 6.0g toluene solution. The system was subjected to liquid nitrogen freezing-vacuumizing-argon filling-thawing repeated operation 3 times, and the system was sealed after 10 minutes of argon gas. The reaction was carried out at 20°C for 5 hours. Terminate the reaction, centrifuge the reaction product, take the precipitate, and wash the precipitate to obtain polytrimethyl-terminated hydroxyethyl methacrylate (PHEMA-tmsn); wherein n is 30.
[0050] (2) Dissolve 1mmol PHEMA-tmsn in 10ml tetrahydrofuran, add 0.1ml 1mol / L hydrochloric acid solution for hydrolysis, react at 30°C for 3 hours, centrifuge the reaction product, take the precipitate, wash the precipitate, and obtain polyhydroxyethyl methacrylate (PHEMAn).
...
Embodiment 2
[0060] A synthetic method for polyhydroxyethyl methacrylate, comprising the following steps:
[0061] (1) In a round bottom flask, add 1mmol 1-phenylethyl chloride, 100mmol hydroxyethyl acrylate, 3mmol cuprous bromide, 3mmol pentamethyldiethylenetriamine and 11.6g anisole solution, and carry out the reaction system Liquid nitrogen freezing-vacuumizing-filling with argon-thawing operation repeated 3 times, argon for 10 minutes and then sealed. The reaction was carried out at 50° C. for 8 hours. Terminate the reaction, centrifuge the reaction product, take the precipitate, and wash the precipitate to obtain polytrimethyl-capped hydroxyethyl acrylate (PHEA-tmsn); wherein n is 70.
[0062] (2) Dissolve 1mmol PHEA-tmsn in 10ml dioxane, add 0.1ml 1mol / L hydrochloric acid solution for hydrolysis, react at 30°C for 6 hours, centrifuge the reaction product, take the precipitate, wash the precipitate, and obtain poly(hydroxyethyl acrylate) Esters (PHEAns).
[0063] (3) Dissolve 1mmol...
Embodiment 3
[0072] A synthetic method for polyhydroxyethyl methacrylate, comprising the following steps:
[0073] (1) In a round-bottomed flask, add 1mmol 1-phenylethyl chloride, 400mmol hydroxyethyl methacrylate, 8mmol cuprous chloride, 8mmol 2'2-bipyridine and 52.1g anisole solution to the reaction system Perform liquid nitrogen freezing-vacuumizing-filling with argon-thawing repeatedly 3 times, and seal it after argon gas for 10 minutes. The reaction was carried out at 80° C. for 15 hours. Terminate the reaction, centrifuge the reaction product, take the precipitate, and wash the precipitate to obtain polytrimethyl-capped hydroxyethyl acrylate (PHEMA-tmsn); wherein n is 280.
[0074] (2) Dissolve 1mmol PHEMA-tmsn in 10ml pyridine, add 0.1ml 1mol / L hydrochloric acid solution for hydrolysis, react at 30°C for 9 hours, centrifuge the reaction product, take the precipitate, wash the precipitate to obtain polyhydroxyethyl methacrylate (PHEMAn).
[0075] (3) Dissolve 1mmol PHEMAn in 5ml d...
PUM
Property | Measurement | Unit |
---|---|---|
thickness | aaaaa | aaaaa |
electrical 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