Graphene-modified premixed emulsion and black conductive coating thereof
A technology of graphene modification and conductive coating, which is applied in the direction of coating, pigment slurry, etc., can solve the problems that are difficult to meet the needs of rapid development, and achieve strong antistatic ability, good temperature resistance and chemical resistance, and simple process Effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0030] A kind of graphene modified water-based silicon acrylic emulsion A, its preparation process is as follows:
[0031] 1) In a four-port reactor equipped with a thermometer, condenser, and agitator, add 3.5 parts of dimethylolpropionic acid and 2.0 parts of special graphene according to the weight of the formula, raise the temperature to 70-75°C, and then slowly drop Add 7.5 parts of isophorone diisocyanate, stir and react for 0.5-1.0 hours, add 0.05 parts of dibutyltin dilaurate in the formula, raise the temperature to 85-88°C and react for 2-2.5 hours, during the reaction, add 3.6 parts of butyl acrylate, methyl Adjust the viscosity with 6.0 parts of methyl acrylate, lower the temperature to 80°C, add 1.8 parts of hydroxyethyl acrylate, continue the reaction for 1.5 hours, and measure the NCO value until it is consistent with the design value;
[0032] 2) Continue to stir to reduce the temperature of the reactant to below 45°C, slowly add 3.6 parts of triethylamine dropwis...
Embodiment 2
[0035] A kind of graphene modified water-based silicon acrylic emulsion B, its preparation process is as follows:
[0036] 1) In a four-port reactor equipped with a thermometer, condenser, and agitator, add 4.0 parts of dimethylolpropionic acid and 2.3 parts of special graphene according to the weight of the formula, raise the temperature to 70-75°C, and then slowly drop Add 7.6 parts of toluene diisocyanate, stir and react for 0.5-1.0 hours, add 0.05 parts of dibutyltin dilaurate in the formula, raise the temperature to 85-88°C and react for 2-2.5 hours, during the reaction, add 4.2 parts of stearyl acrylate, methyl acrylate 7.0 parts to adjust the viscosity, lower the temperature to 80°C, add 2.0 parts of hydroxyethyl acrylate, continue the reaction for 1.5 hours, and measure the NCO value until it is consistent with the design value;
[0037] 2) Continue to stir to reduce the temperature of the reactant to below 45°C, slowly add 4.2 parts of triethylamine dropwise under hig...
Embodiment 3
[0040] A kind of fluorine-containing polyurethane modified acrylic water-based resin C, its preparation process is as follows:
[0041] a. In a four-port reactor equipped with a thermometer, condenser, and agitator, add 3.0 parts of butanediol, 1.5 parts of trimethylolpropane, 7.0 parts of polytetrahydrofuran polyol, dimethylol 2.6 parts of propionic acid, heated to 95-110°C for vacuum dehydration for 1.5-2.0 hours;
[0042] b. Cool down to 60~70℃, 10.0 parts of hexamethylene diisocyanate, pass through N 2 , then dropwise add 0.05 parts of dibutyltin dilaurate in the formula, raise the temperature to 80-82° C. and react for 1-1.5 hours to obtain the hydrophilic polyurethane prepolymer;
[0043] c. Prepare 9.0 parts of methyl methacrylate and 3.0 parts of butyl methacrylate in advance, take 6.0 parts of the acrylate mixture and add it to the hydrophilic polyurethane prepolymer until the viscosity is moderate, cool down to 70°C, add 2.0 parts of hydroxyethyl acrylate, continue...
PUM
Property | Measurement | Unit |
---|---|---|
electrical resistance | 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