Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Preparation method of ultraviolet-curable organosilicone-modified pressure-sensitive adhesive

A silicone, pressure-sensitive adhesive technology, applied in the direction of adhesives, graft polymer adhesives, adhesive types, etc., can solve problems such as environmental pollution and energy waste

Inactive Publication Date: 2013-06-19
YANTAI DARBOND TECH
View PDF8 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The technical problem to be solved by the present invention is: a large amount of organic solvents are used in the production process of the traditional silicone pressure-sensitive adhesive, which is easy to cause environmental pollution and energy waste. When using, it needs to be coated at high temperature

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 ultraviolet-curable organosilicone-modified pressure-sensitive adhesive
  • Preparation method of ultraviolet-curable organosilicone-modified pressure-sensitive adhesive

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] Add 120 grams of biscarboxysilane oil with a hydroxyl value of 60 (Dow Corning BY16-201) and 17 grams of isophorone diisocyanate into the reactor, add 0.1 grams of dibutyltin dilaurate as a catalyst, and react at 75 ° C for 2.5 hour, add 3.5 g of hydroxyethyl acrylate and 0.3 g of p-hydroxyanisole, continue to react at 75 ° C for 2 hours, then add 30 g of isooctyl acrylate, stir evenly, cool and discharge the prepolymer [1].

[0039] Mix 30 grams of C5 petroleum resin (softening point 90°C) with 4 grams of tetraethylene glycol diacrylate and 20 grams of tetrahydrofuryl acrylate, heat to 40°C, stir to dissolve, add the above prepolymer[1] 100 grams, add 5 grams of 2-hydroxy-methylphenylpropan-1-one as a photoinitiator, mix to maintain the viscosity of the system at 2000mPa.s, evenly apply it on a PET film, and place it under a 2Kw ultraviolet lamp for 15 cm Cured for 50 seconds.

Embodiment 2

[0041] Add 150 grams of biscarboxysilane oil with a hydroxyl value of 35 (Shin-Etsu KF6002) and 15.6 grams of isophorone diisocyanate into the reactor, add 0.2 grams of dibutyltin dilaurate as a catalyst, and react at 75 ° C for 2.5 hours. Add 6.2 g of hydroxyethyl acrylate and 0.3 g of p-hydroxyanisole, continue to react at 75°C for 2 hours, then add 30 g of isooctyl acrylate, stir evenly, cool and discharge to form a prepolymer [2].

[0042]Mix 30 grams of C5 petroleum resin (softening point 90°C) with 4 grams of tetraethylene glycol diacrylate and 20 grams of tetrahydrofuryl acrylate, heat to 40°C, stir to dissolve, add the above prepolymer[2] 100 grams, add 5 grams of 2-hydroxy-methylphenylpropan-1-one as a photoinitiator, mix to maintain the viscosity of the system at 3000mPa.s, evenly apply it on a PET film, and place it under a 2Kw ultraviolet lamp for 15 cm Cured for 50 seconds.

Embodiment 3

[0044] Add 160 grams of biscarboxysilane oil with a hydroxyl value of 22 (Shin-Etsu KF6003) and 12.6 grams of isophorone diisocyanate into the reactor, add 0.2 grams of dibutyltin dilaurate as a catalyst, and react at 75°C for 2.5 hours. Add 6.7 g of hydroxyethyl acrylate and 0.3 g of p-hydroxyanisole, continue to react at 75°C for 2 hours, then add 30 g of isooctyl acrylate, stir evenly, cool and discharge to form a prepolymer [3].

[0045] Mix 30 grams of C5 petroleum resin (softening point 90°C) with 4 grams of tetraethylene glycol diacrylate and 20 grams of tetrahydrofuryl acrylate, heat to 40°C, stir to dissolve, add the above prepolymer[3] 100 grams, add 5 grams of 2-hydroxy-methylphenylpropan-1-one as a photoinitiator, mix to maintain the viscosity of the system at 4000mPa.s, evenly apply it on a PET film, and place it under a 2Kw ultraviolet lamp for 15 cm Cured for 50 seconds.

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
viscosityaaaaaaaaaa
softening pointaaaaaaaaaa
viscosityaaaaaaaaaa
Login to View More

Abstract

The invention relates to a preparation method of a pressure-sensitive adhesive, and particularly relates to a preparation method of a solvent-free ultraviolet-curable organosilicone-modified pressure-sensitive adhesive. The method comprises the steps of: preparation of an organosilicone-modified polyurethane acrylate prepolymer and preparation of the pressure-sensitive adhesive. The pressure-sensitive adhesive is free of any organic solvents, and can be coated at normal temperature, dried without heating and rapidly cross-linked and cured.

Description

technical field [0001] The invention relates to a silicone pressure-sensitive adhesive and a preparation method thereof, in particular to a solvent-free UV-cured silicone-modified pressure-sensitive adhesive. Background technique [0002] Silicone pressure-sensitive adhesives are a kind of high-quality special pressure-sensitive adhesives in pressure-sensitive adhesives. The current silicone pressure-sensitive adhesives, such as silanol condensation type silicone pressure-sensitive adhesives, are suitable for silicone pressure-sensitive adhesives used under high temperature and harsh conditions. glue system. This pressure-sensitive adhesive is usually composed of silicone rubber, MQ silicone resin, organic solvents and other additives. The organic solvent used is generally toluene or xylene, and a large amount of volatile organic compounds (VOC) are eliminated during the coating process. These substances not only cause serious environmental pollution, but also pose a threa...

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): C09J151/08C08G18/61
Inventor 崔亨利王建斌陈田安
Owner YANTAI DARBOND TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products