Waterborne polyurethane primer for coating plastic film and preparation method thereof
A water-based polyurethane and plastic film technology, applied in the direction of polyurea/polyurethane adhesives, adhesives, adhesive types, etc., can solve the problems of restricting the development of coating films, operators' physical and environmental hazards, and unsatisfactory use conditions
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0028] 1. Add 3.6 kilograms of polycaprolactone diol and 0.3 kilograms of dimethylol propionic acid to the reaction vessel, and feed N 2 protection, stirring and raising the temperature to 70° C., adding 0.24 kg of isophorone diisocyanate and reacting for 1 hour to prepare prepolymer A.
[0029] 2. Dissolve 0.03 kg of diethylenetriamine and 0.3 kg of ammonia water in 22.16 kg of water to form mixed solution B.
[0030] 3. Slowly add the mixed solution B into the prepolymer A, and add 1.2 kg of N-methylpyrrolidone to adjust the viscosity of the emulsion to 12s. At this time, the amount of N-methylpyrrolidone added accounted for 4.5% of the total mass of the prepolymer A and the mixed solution B. At room temperature, increase the rotation speed to 2000 rpm, raise the temperature to 40°C, and keep it for 1 hour.
[0031] 4. Reduce to normal temperature, vacuumize (-0.08MPa) and distill under reduced pressure to remove the organic solvent, finally add 0.015 kg of 1,2-benzisothia...
Embodiment 2
[0034] 1. Add 5.6 kg of polycarbonate diol and 0.8 kg of dimethylol butyric acid to the reaction vessel, and feed N 2 protection, stirring and raising the temperature to 75° C., adding 3.6 kg of tetramethylxylylene diisocyanate and reacting for 1.2 hours to prepare prepolymer A.
[0035] 2. Dissolve 0.12 kg of ethylenediamine and 0.8 kg of triethylamine in 27.45 kg of water to form mixed solution B.
[0036] 3. Slowly add the mixed solution B to the prepolymer A, and add 1.6 kg of N-methylpyrrolidone to adjust the viscosity of the emulsion to 14s. Wherein, the addition amount of N-methylpyrrolidone accounts for 4.2% of the total mass of the prepolymer A and the mixed solution B. At room temperature, increase the rotation speed to 2100 rpm, raise the temperature to 42°C, and keep it for 2 hours.
[0037] 4. Reduce to normal temperature, vacuumize (-0.08MPa) and distill under reduced pressure to remove the organic solvent, finally add 0.032 kg of 1,2-benzisothiazol-3-one, stir...
Embodiment 3
[0040] 1. Add 4.8 kilograms of polycaprolactone diols, 4.8 kilograms of polycarbonate diols, and 1.5 kilograms of 1,4-butanediol-2-sodium sulfonate in the reaction vessel, feed N 2 protection, stirring and raising the temperature to 78°C, adding 6 kg of hexamethylene diisocyanate and reacting for 1.5 hours to prepare prepolymer A.
[0041] 2. Dissolve 0.3 kg of hydrazine and 1.5 kg of triethylamine in 38.52 kg of water to form mixed solution B.
[0042] 3. Slowly add the mixed solution B into the prepolymer A, and add 2.52 kg of N-methylpyrrolidone to adjust the viscosity of the emulsion to 16s. Wherein, the addition amount of N-methylpyrrolidone accounts for 4.4% of the total mass of the prepolymer A and the mixed solution B. At room temperature, increase the rotation speed to 2300 rpm, raise the temperature to 43°C, and keep it for 2.2 hours.
[0043] 4. Reduce to normal temperature, vacuumize (-0.08MPa) and distill under reduced pressure to remove the organic solvent, final...
PUM
Property | Measurement | Unit |
---|---|---|
peel strength | aaaaa | aaaaa |
strength | aaaaa | aaaaa |
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