Ultraviolet light polymerization adhesive and preparation method thereof

A UV light and adhesive technology, which is applied in the direction of adhesives, adhesive types, polyurea/polyurethane adhesives, etc., can solve the problems of difficult deep curing of UV curing adhesives, limited penetration depth of UV rays, and health hazards to operators, etc. , to achieve the effect of eliminating oxygen resistance, excellent cohesive energy, and improving flexibility

Active Publication Date: 2014-05-28
CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
View PDF9 Cites 27 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] However, the use of α-cyanoacrylate substances in the prior art will cause certain health hazards to operators; at the same time, unsaturated resin is used as the matrix resin, and the glue layer of the UV-curable adhesive is caused due to the relatively thick glue layer. It is difficult to cure completely, and the penetration depth of ultraviolet rays is limited, coupled with the "oxygen inhibition" effect, it is difficult to cure deep UV curing adhesives, resulting in poor bonding performance of the adhesive layer

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
  • Ultraviolet light polymerization adhesive and preparation method thereof
  • Ultraviolet light polymerization adhesive and preparation method thereof
  • Ultraviolet light polymerization adhesive and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0035] The invention provides a preparation method of polydimethylsiloxane mercaptoacrylate, which is characterized in that it comprises the following steps: polydimethylsiloxane with terminal hydroxyl group, carboxylic acid containing mercapto group, p-toluenesulfonic acid and The reaction is carried out with an organic solvent not containing active hydrogen atoms to obtain polydimethylsiloxane mercaptoacrylate.

[0036]The carboxylic acid containing mercapto is preferably mercaptopropionic acid or mercaptoacetic acid; the organic solvent without active hydrogen atoms is preferably toluene, xylene, cyclohexanone, acetone or butanone, more preferably toluene, cyclohexanone or butanone; the number average molecular weight of the hydroxyl-terminated polydimethylsiloxane is preferably 1000 to 4000, more preferably 2000 to 3000; the hydroxyl-terminated polydimethylsiloxane, carboxylic acid containing mercapto, The mass ratio of p-toluenesulfonic acid and the organic solvent withou...

Embodiment 1

[0072] Preparation of High Functional Polyurethane Acrylate

[0073] (a) Under the protection of nitrogen, add 100g number-average molecular weight to the three-necked bottle that is 1000 hydroxyl-terminated polybutadiene liquid rubber and 50g number-average molecular weight is the polybutylene adipate diol of 1000, is heated to 110 ℃, dehydrate at -0.98MPa for 1 hour, then lower the temperature to 75℃, under nitrogen protection, add 0.12g dibutyltin dilaurate and 10.6g trimethylolpropane, add 68g of 2,4 - Toluene diisocyanate, after the dropwise addition, reacted for 2 hours to obtain the first intermediate.

[0074] (b) Under the protection of nitrogen, the first intermediate obtained by the above reaction was warmed up to 85° C., and reacted for 1 hour; then 0.46 g of p-hydroxyanisole was added, and 130 g of pentaerythritol triacrylate was added dropwise at a speed of 6 ml / min, After the dropwise addition was completed, the reaction was continued for 2 hours to obtain a hi...

Embodiment 2

[0076] Preparation of High Functional Polyurethane Acrylate

[0077] (a) Under the protection of nitrogen, add 320g number average molecular weight to the three-necked bottle that is the polybutylene adipate diol that the number average molecular weight of 5000 is 5000 and the polybutylene adipate diol that 106g number average molecular weight is 6000, is heated to 120 ℃, dehydrate at -0.98MPa for 3 hours, lower the temperature to 80°C, under nitrogen protection, add 0.56g stannous octoate and 18.1g trimethylolpropane, drop 140g diphenylmethane-4 at a speed of 10ml / min, 4-diisocyanate, after the dropwise addition, reacted for 4 hours to obtain the first intermediate.

[0078] (b) Under nitrogen protection, the first intermediate obtained by the above reaction was warmed up to 90° C., and reacted for 3 hours; then 0.72 g of hydroquinone was added, and 264 g of dipentaerythritol pentaacrylate was added dropwise at a speed of 15 ml / min, After the dropwise addition, the reaction ...

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

PropertyMeasurementUnit
shear strengthaaaaaaaaaa
peel strengthaaaaaaaaaa
shear strengthaaaaaaaaaa
Login to view more

Abstract

The invention provides an ultraviolet light polymerization adhesive and a preparation method thereof. The ultraviolet light polymerization adesive is prepared from the following components in parts by weight: 236-385 parts of polyurethane acrylate, 0.82-1.35 parts of polydimethylsiloxane mercapto acrylate, 43-82 parts of a monofunctional reactive diluent, 72-105 parts of a polyfunctional reactive diluent, 11.8-19.3 parts of a photoinitiator, 0.46-0.84 part of an ultraviolet light absorbent, 0.92-1.78 parts of a leveling agent, 1.03-1.92 parts of a foam killer and 0.48-0.86 part of a silane coupling agent. The ultraviolet light polymerization adhesive provided by the invention has better high-temperature impact resistance and excellent adhesion, has no cyano group, and is environment-friendly and nontoxic.

Description

technical field [0001] The invention relates to the technical field of adhesives, in particular to an ultraviolet light curing adhesive and a preparation method thereof. Background technique [0002] Adhesives, also known as adhesives or adhesives, refer to organic or A class of substances that are inorganic, natural, or synthetic. The adhesive has the characteristics of continuous stress distribution, light weight, tightness, and low process temperature, and is especially suitable for the connection of different materials, different thicknesses, ultra-thin specifications, and complex components. [0003] Adhesives can be divided into light-curable, thermosetting, hot-melt, room temperature-curable, pressure-sensitive, etc. according to the application method. Among them, light-curable adhesives mainly include visible light, ultraviolet light and electron beam curing adhesives. At present, researchers The most concerned is the UV-curable adhesive. [0004] UV curable adhe...

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 Applications(China)
IPC IPC(8): C08G77/392C09J175/14C09J11/08C08G18/69C08G18/67C08G18/66C08G18/42
Inventor 张红明赵强李季王献红王佛松
Owner CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap