Unlock instant, AI-driven research and patent intelligence for your innovation.

Preparation method of water-based polyurethane acrylate (WPUA) silicon dioxide photocureable coating

A urethane acrylate and light-curing coating technology, applied in the direction of coating, can solve the problems of affecting promotion, easy agglomeration of emulsions, poor stability, etc., and achieve the effects of excellent mechanical properties, simple preparation process, and improved performance

Inactive Publication Date: 2013-05-08
JIANGSU UNIV
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the method of blending makes the emulsion obtained by modifying silica to polyurethane coatings easy to agglomerate, and the stability is not good, which affects its further promotion.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation method of water-based polyurethane acrylate (WPUA) silicon dioxide photocureable coating

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0014] In a container equipped with a stirring device, add 0.6mol absolute ethanol, the 0.1mol Add n-butyl silicate into the container, stir at room temperature for 1 hour, then raise the temperature to 50°C and slowly drop into the container containing 0.01mol Hydrochloric acid in deionized water 0.6mol , react for 1h to get n-butyl silicate sol.

[0015] Add 16.664g of polyether polyol (NJ-210) and 2.316g of dimethylol propionic acid (DMPA) into a 500mL four-necked bottle equipped with a stirrer, reflux condenser, thermometer and feeding device; add 1.68g N-methylpyrrolidone (NMP) solvent, raise the temperature of the system to 60°C, add 9.99g of isophorone diisocyanate (IPDI), dropwise add catalyst 0.0876g of dibutyltin dilaurate (T-12), stir for 30min Finally, raise the temperature of the system to 80°C (if the viscosity of the system is too high, add a certain amount of acetone), continue the reaction for 4 hours, then lower the temperature to 60°C, add 3.348g of h...

Embodiment 2

[0017] In a container equipped with a stirring device, add 0.6mol absolute ethanol, the 0.1mol Add n-butyl silicate into the container, stir at room temperature for 1 hour, then raise the temperature to 50°C and slowly drop into the container containing 0.01mol Hydrochloric acid in deionized water 0.6mol, react for 1h to get n-butyl silicate sol.

[0018] Add 16.394g of polyether polyol (NJ-220), 1.639g of N-methylpyrrolidone (NMP) and 1.228g of dihydroxy Add methacrylic acid (DMPA) into the reaction device, raise the temperature of the system to 60°C, add 6.938g of isophorone diisocyanate (IPDI), dropwise add the catalyst 0.098g of dibutyltin dilaurate (T-12), After stirring for 30 minutes, raise the temperature of the system to 80°C (if the viscosity of the system is too high, add a certain amount of acetone), continue the reaction for 4 hours, then lower the temperature to 60°C, add 3.611g of hydroxyethyl methacrylate (HEMA), After reacting for 5 hours, lower the te...

Embodiment 3

[0020] In a container equipped with a stirring device, add 0.6mol absolute ethanol, the 0.1mol Add n-butyl silicate into the container, stir at room temperature for 1 hour, then raise the temperature to 50°C and slowly drop into the container containing 0.01mol Hydrochloric acid in deionized water 0.6mol , react for 1h to get n-butyl silicate sol.

[0021] Add 13g of polyether polyol NJ-210, 1.528g of dimethylol propionic acid (DMPA) and 1.3g of N-methyl Pyrrolidone (NMP) solvent, raise the temperature of the system to 60°C, add 10.823g of isophorone diisocyanate (IPDI), dropwise add the catalyst 0.051g of dibutyltin dilaurate (T-12), stir for 30min, and put the system The temperature rises to 80°C (if the viscosity of the system is too high, a certain amount of acetone can be added), after continuing the reaction for 4 hours, the temperature is lowered to 60°C, and 6.338g of hydroxyethyl methacrylate (HEMA) is added, and the temperature is lowered after 5 hours of reac...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention discloses a preparation method of a water-based polyurethane acrylate (WPUA) silicon dioxide photocureable coating, relating to a preparation technology for modifying a water-based polyurethane acrylate emulsion. A WPUA / nano-SiO2 photocureable coating is prepared with a sol-gel method, the preparation process is simple, a silane coupling agent KH560 is selected, uniform dispersion of nanoparticles can be realized, and a good interface bonding layer is formed on the surface of the coating, so that the WPUA coating has high mechanical property and the specific enhancing and toughening properties of a nanomaterial; and meanwhile, nano-SiO2 particles are introduced, so that the weather resistance, mechanical property, coating transparency and the like of a hybrid material are enhanced greatly.

Description

technical field [0001] The invention relates to a preparation technology for water-based polyurethane acrylate emulsion modification, in particular to a preparation method for water-based polyurethane acrylate / nanometer silica photocuring hybrid material. Background technique [0002] UV-curable coatings have the advantages of fast curing, environmental protection, and energy saving. They are one of the outstanding representatives of modern industrialized mass-production coatings. However, UV-curable coatings also have some disadvantages. For example, photo-curable materials are limited by light penetration, and are only suitable for composite materials composed of transparent reinforcing materials and transparent resins. At the same time, excessive photoinitiators are often added to photocurable coatings. After these residual initiators are irradiated by light, the free radicals generated will accelerate the aging of materials. Moreover, due to the cross-linking and shrink...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C08G18/12C08G18/67C08G18/66C08F290/06C09D151/08
Inventor 邱凤仙许和平杨冬亚郭卿
Owner JIANGSU UNIV