Ionic conductive hydrogel as well as preparation method and application thereof
A technology of ion conduction and hydrogel, applied in application, diagnostic recording/measurement, diagnosis, etc. Repair ability and other problems, achieve excellent mechanical sensing performance, prolong service life and function, and stabilize resistance change
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0036] The design idea of the preparation method of the ion-conductive hydrogel of the present invention is as follows: firstly, a phenylboronic acid ionic liquid monomer is designed to endow the hydrogel with excellent multifunctional properties. As a multifunctional monomer, three main structural designs were considered: (1) dynamic borate bond formation between phenylboronic acid and cis-diol; (2) imidazolium salt structure, which can increase the hydrogel ionic conductivity, and can produce hydrogen bonds and electrostatic interactions with other components in the system; (3) the vinyl group in the imidazolium cation is conducive to the firm bonding of multifunctional monomers in the hydrogel network. Secondly, TEMPO-oxidized nanocellulose is selected as the stress-enhanced phase to improve the mechanical strength of the hydrogel. On the one hand, the hydroxyl groups on the nanocellulose can dynamically reversibly combine with the boric acid functional groups in the pheny...
Embodiment 1
[0045] The preparation method of the ion-conductive hydrogel of the present invention specifically comprises the following steps:
[0046] Step 1, preparation of phenylboronic acid ionic liquid monomer: step 1.1, dissolve 0.4297g PBA in 15mL ethyl acetate, continue to stir and sonicate until it is completely dissolved, and obtain solution A; step 1.2, in magnetic stirring solution A Under conditions, after adding 226IL, continue to stir until it is completely dissolved to obtain solution B; step 1.3, the resulting solution B is passed through N 2 reaction at 70°C for 20 hours to obtain mixture C; step 1.4, add 45 mL of ethyl acetate to the mixture C obtained in step 1.3 in 3 times, and carry out rotary evaporation at 35°C until the ethyl acetate is completely evaporated to dryness, that is Product A was obtained, and the product A was vacuum-dried at 45° C. to obtain phenylboronic acid ionic liquid monomer (PBA-IL).
[0047] Step 2, preparation of multifunctional ion-conducti...
Embodiment 2
[0052] The preparation method of the ion-conductive hydrogel of the present invention specifically comprises the following steps:
[0053] Step 1, preparation of phenylboronic acid ionic liquid monomer: step 1.1, dissolve 0.4297g PBA in 15mL ethyl acetate, continue to stir and sonicate until it is completely dissolved, and obtain solution A; step 1.2, in magnetic stirring solution A Under conditions, after adding 226IL, continue to stir until it is completely dissolved to obtain solution B; step 1.3, the resulting solution B is passed through N 2 reaction at 70°C for 20 hours to obtain mixture C; step 1.4, add 45 mL of ethyl acetate to the mixture C obtained in step 1.3 in 3 times, and carry out rotary evaporation at 35°C until the ethyl acetate is completely evaporated to dryness, that is Product A was obtained, and the product A was vacuum-dried at 45° C. to obtain phenylboronic acid ionic liquid monomer (PBA-IL).
[0054] Step 2, preparation of ion-conducting hydrogel:
...
PUM
Property | Measurement | Unit |
---|---|---|
breaking strength | aaaaa | aaaaa |
breaking strength | aaaaa | aaaaa |
tensile strength | 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