Unsaturated polyether, light-cured resin and preparation method of unsaturated polyether

A technology of unsaturated polyether, which is applied in the field of unsaturated polyether, photocurable resin and its preparation, can solve the problems of long curing time and achieve the effects of fast photocuring speed, high crosslinking density and excellent adhesion performance

Active Publication Date: 2017-12-01
SHENZHEN GRADUATE SCHOOL TSINGHUA UNIV
View PDF7 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The polyurethane acrylate synthesized by this method has the advantages of high functionality, strong polarity, high strength and low viscosity, but its curing time is long, and its curing time is 70-110s when tested by finger dry method

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
  • Unsaturated polyether, light-cured resin and preparation method of unsaturated polyether
  • Unsaturated polyether, light-cured resin and preparation method of unsaturated polyether
  • Unsaturated polyether, light-cured resin and preparation method of unsaturated polyether

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0023] In this specific embodiment, a preparation method of unsaturated polyether is provided, comprising the following steps: adding a dihydric alcohol or a polyhydric alcohol as an initiator in a reaction vessel, adding an active metal cation catalyst, vacuum dehydration treatment, passing an inert gas, adding a chain extender to the reaction vessel, the chain extender is glycidyl ether containing unsaturated bonds, glycidyl ester containing unsaturated bonds, glycidyl ether with photoactivity or glycidyl ether with photoactivity Glycerides; control the temperature of the reaction system at 0-140°C, and carry out ring-opening polymerization for 0.5-3 hours at a stirring speed of 300-500 rpm to prepare unsaturated polyether.

[0024] Wherein, the initiator is dihydric alcohol or polyhydric alcohol.

[0025] The chain extender is one or a mixture of glycidyl methacrylate, glycidyl methacrylate, glycidyl acrylate, glycidyl acrylate, allyl glycidyl ether, and allyl glycidyl este...

Embodiment 1

[0042] Weigh 0.1 mol (7.609 g) of propylene glycol and 0.8529 g of potassium hydroxide (active cationic catalyst) and add them into the reaction vessel. Vacuum dehydration at 80°C for 30 min. Nitrogen gas was introduced to maintain a certain nitrogen flow rate. Slowly add 0.6 mol (85.29 g) of glycidyl acrylate dropwise into the reaction vessel, and the dropping time is controlled within 30-60 minutes. After the glycidyl acrylate was added dropwise, the reaction was continued for 1 h. Stop heating, and neutralize the system with 0.1mol / L phosphoric acid aqueous solution until the pH of the system is neutral. Add 20ml of deionized water, stir at room temperature for 30min, distill under reduced pressure to remove the water in the system, wash the system with petroleum ether, and distill under reduced pressure to remove the petroleum ether in the system to obtain a hydroxyl-terminated unsaturated polyether.

[0043] Such as figure 1 Shown is the NMR spectrum of the prepared h...

Embodiment 2

[0048] Weigh 0.17mol (12.94g) of propylene glycol into the reaction vessel, and vacuum dehydrate at 80°C for 30min. Nitrogen gas was introduced to maintain a certain nitrogen flow rate. Cool down to 65°C, add 1.135ml of cocatalyst trifluoroacetic acid into the reaction vessel, add 0.800ml of catalyst anhydrous tin tetrachloride into the reaction vessel, slowly add 1.02mol (145g) glycidyl acrylate dropwise into the reaction vessel For ester, the dropping time is controlled within 30-60min. After the glycidyl acrylate was added dropwise, the reaction was continued for 4h. Stop heating, add 150ml of dichloroethane, and let stand overnight (stand for about 24h). Filter to remove the lower layer liquid. Wash three times with methanol aqueous solution of disodium ethylenediamine tetraacetate, distill under reduced pressure, remove dichloroethane and water in the system, and obtain unsaturated polyether with terminal hydroxyl groups.

[0049] The hydroxyl-terminated unsaturated p...

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
gel rateaaaaaaaaaa
Login to view more

Abstract

The invention discloses an unsaturated polyether, a light-cured resin and a preparation method of the unsaturated polyether. The preparation method of the unsaturated polyether comprises the steps of adding diol or polyol, used as an initiator, into a reaction container, adding an active metal cationic catalyst, vacuum dehydrating, introducing an inert gas, and adding a chain extender into the reaction container, wherein the chain extender is glycidyl ether containing unsaturated bonds, glycidyl ester containing unsaturated bonds, glycidyl ether with optical activity or glycidyl ester with optical activity; and controlling a temperature of a reaction system at 0-140 DEG C, and performing ring-opening polymerization for 0.5-3 hours at a stirring speed of 300-500rpm, so as to prepare the unsaturated polyether. The unsaturated polyether prepared by the method can effectively shorten the curing time of the prepared UV-cured resin, improves the cross-linking density of the light-cured resin, and improves the performance of the light-cured resin.

Description

【Technical field】 [0001] The invention relates to an unsaturated polyether, a photocurable resin and a preparation method thereof. 【Background technique】 [0002] UV curing is a material surface treatment technology that appeared in the 1960s. It refers to the crosslinking of liquids with photocurable activity under ultraviolet light to form solid materials. UV curing technology has many advantages. For example, compared with other technologies, UV curing technology has a particularly fast curing speed. The curing time of UV curing technology is generally about tens of seconds, which is difficult for other curing technologies to achieve. The earliest industrialization of UV curing was in 1968, when Bayer of Germany developed a UV curing coating whose main components were unsaturated polyester and styrene. Now the application range of UV curing technology is expanding, including coatings, inks, adhesives and so on. [0003] UV curing products are composed of oligomers, reac...

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): C08G65/28C08F2/48
CPCC08F2/48C08G65/002C08G65/2606
Inventor 唐国翌朱亚丽董运生姚有为陈丽杰
Owner SHENZHEN GRADUATE SCHOOL TSINGHUA UNIV
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