Polyurethane or polyurethane-urea aqueous dispersion with excellent heat-damp resistance performance, and preparation method and application thereof
A polyurethane and dispersion technology, applied in polyurea/polyurethane adhesives, adhesive types, adhesives, etc., can solve problems such as no self-crosslinking performance, unstable storage of dispersions, and slow crosslinking reaction speed
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0095] 210g dehydration treated polyester I (component c)), 28.35g isocyanate I (component d)), 2g dehydration treated polyether I (component f)), 23g acetone (organic solvent), 0.04g Bismuth neodecanoate (catalyst) was added into a 1L four-neck round bottom flask equipped with a nitrogen inlet and outlet, and the mixture was stirred at 80-90° C. until NCO reached 2.00%. The prepolymer was dissolved in 400 g of acetone and cooled to 50°C. Dissolve 4.63g N-(2-aminoethyl)-2-aminoethanesulfonic acid sodium (component e)), 3.26g isophoronediamine (component e)), 0.86g hydroxyethyl ethyl 35 g aqueous solution of diamine (component g)) and 5 g acetone solution dissolved with 0.5 g N-β-(aminoethyl)-γ-aminopropyltrimethoxysilane (component a)) and dissolved with 1.1 g A solution of 6 g of bis(3-triethoxysilylpropyl)amine (component b)) in acetone was added separately to the acetone solution in which the prepolymer was dissolved with vigorous stirring. After stirring for 20 min, the ...
Embodiment 2
[0097] Add 150g of dehydrated polyester I, 60g of dehydrated polyester II, 28.5g of isocyanate I, 24g of acetone, 0.04g of bismuth neodecanoate, and 3.15g of polyether II into a 1L four-port port equipped with nitrogen inlet and outlet. In a round bottom flask, the mixture was stirred at 80-90°C until the NCO reached 1.95%. The prepolymer was dissolved in 405 g of acetone and cooled to 50°C. 10 g of aqueous solution and 2.39 g of N-β 20g of acetone solution of -(aminoethyl)-γ-aminopropyltrimethoxysilane and 6g of acetone solution of 1.1g of bis(3-triethoxysilylpropyl)amine dissolved in The acetone solution of the prepolymer was stirred vigorously. After stirring for 20 min, the mixture was dispersed by adding 197 g of water. After the acetone had been separated off by distillation, 4 g of emulsifier Tween 20 were added. A solvent-free aqueous dispersion of polyurethane-polyurea was obtained with a number-average molecular weight of 90,000 by GPC, a solids content of 55% by...
Embodiment 3
[0099] 80g of dehydrated polyester I, 25g of dehydrated polyester III, 20g of dehydrated polyester IV, 2g of dehydrated polyether I, 22g of isocyanate I, 18g of acetone, 0.04g of bismuth neodecanoate Add it into a 1L four-necked round-bottom flask equipped with a nitrogen inlet and outlet, and stir the mixture at 80-90° C. until NCO reaches 2.1%. The prepolymer was dissolved in 309 g of acetone and cooled to 50°C. 35g aqueous solution and 0.5g N-β -(Aminoethyl)-γ-aminopropyltrimethoxysilane 5g acetone solution and 2g bis(3-triethoxysilylpropyl)amine dissolved in 10g acetone solution were added to the pre-dissolved Polymer in acetone solution while stirring vigorously. After stirring for 20 min, the mixture was dispersed by adding 224 g of water. After the acetone had been separated off by distillation, 4 g of emulsifier Tween 20 were added. Obtained the aqueous dispersion of the polyurethane-polyurea of solvent-free, its number-average molecular weight is measured 110000...
PUM
Property | Measurement | Unit |
---|---|---|
Number average molecular weight | 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