A kind of fluorine-containing polyurethane and preparation method thereof

A technology of polyurethane and fluorine-containing alkyl polyether, applied in the field of polyurethane, can solve problems such as insufficient weather resistance and water resistance, reduce the mechanical properties of polyurethane products, and fail to reach modified polyurethane, etc. Cured, easy to store effect

Active Publication Date: 2019-05-17
UPCHEM CHINA
View PDF7 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the traditional polyurethane materials have insufficient weather resistance and water resistance. Since these polyurethanes use diisocyanates containing aromatic ring structures as the reactant, the products often turn yellow and produce macromolecules when they are exposed to ultraviolet light for a long time outdoors. degradation
When fluorine-containing polyurethane is prepared by addition and chain extension of small-molecule fluorine-containing diols and diisocyanates, the weather resistance of the product can be improved, but the use of small-molecule diols reduces the mechanical properties of polyurethane products, reduces the The amount of alcohol can not achieve the purpose of modifying polyurethane

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
  • A kind of fluorine-containing polyurethane and preparation method thereof
  • A kind of fluorine-containing polyurethane and preparation method thereof
  • A kind of fluorine-containing polyurethane and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0038] (1) Synthesis of nonafluorooxetane monomer

[0039] In a 1000mL three-necked flask equipped with a thermometer, ice-water bath and magnetic stirrer protection, add 16.1g of butyl acetate, 26.2g of sodium bicarbonate, 55.8g of sodium dithionite, 227g of N,N-dimethylformamide, 202g of water, 55.3g of perfluorobutyl iodide was added dropwise, reacted at -13°C for 3h, slowly raised to room temperature, and kept for 2h. After the reaction was completed, extraction was performed three times with 180 g of toluene. The extracts were combined, washed 3 times with water to obtain a solution of 4-nonafluorobutyl-3-iodobutyl acetate, which was added to a 1000mL three-necked flask, and 310g of sodium hydroxide solution with a mass concentration of 20% was added dropwise and kept at React at 12°C for 3h. After the reaction, the layers were separated. The organic layer was washed three times with water, dried and distilled under reduced pressure to obtain 32.6 g of 3-(1H,1H-nonaflu...

Embodiment 2

[0047] (1) Synthesis of nonafluorooxetane monomer

[0048] In a 1000mL three-necked flask equipped with a thermometer, ice-water bath and magnetic stirrer protection, add 16.5g of butyl acetate, 26.4g of sodium bicarbonate, 53.6g of sodium dithionite, 230g of N,N-dimethylformamide, 210g of water was added dropwise with 55.5g of perfluorobutyl iodide, reacted at -15°C for 3h, slowly raised to room temperature, and kept for 2h. After the reaction was completed, extraction was performed three times with 180 g of toluene. The extracts were combined, washed 3 times with water to obtain a solution of 4-nonafluorobutyl-3-iodobutyl acetate, which was added to a 1000mL three-necked flask, and 310g of sodium hydroxide solution with a mass concentration of 20% was added dropwise and kept at React at 11°C for 3h. After the reaction, the layers were separated. The organic layer was washed three times with water, dried and distilled under reduced pressure to obtain 34.2 g of 3-(1H,1H-non...

Embodiment 3

[0056] (1) Synthesis of tridecafluorooxetane monomer

[0057] In a 1000mL three-necked flask equipped with a thermometer, ice-water bath and magnetic stirrer protection, add 16.5g of butyl acetate, 28.2g of sodium bicarbonate, 55.5g of sodium dithionite, 221g of N,N-dimethylformamide, 230g of water, 73.0g of perfluorohexyl iodide was added dropwise, and the addition was completed in 50 minutes. After the addition, it was reacted at -12°C for 6 hours, slowly raised to room temperature, and kept for 3 hours. After the reaction was finished, extract with 180g trifluorotoluene in 3 times. The extracts were combined and washed 3 times to obtain a 4-tridecafluorohexyl-3-iodobutyl acetate solution. The solution was directly added to a 1000mL three-necked flask, and 550g of mass concentration was added dropwise to a 10% sodium hydroxide solution. Insulate and react at 13°C for 8h. After the reaction, the layers were separated. The organic layer was washed three times with water, dr...

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 fluorine-containing polyurethane and a preparation method thereof. Addition polymerization reaction of fluorine-containing alkyl polyether diol and diisocyanate, catalyzed by tin catalyst, chain extension by chain extender, adding aminosilane coupling agent to end capping, to prepare a fluorine-containing polyurethane; the product has Fluorine-containing polyether block, high fluorine content, the fluoroalkyl group located in the polyether side group is prone to microphase separation and surface migration, low surface energy of polyurethane, fluorine-containing polyurethane is terminated with silane coupling agent, easy to store and easy to cure . The coating prepared by the fluorine-containing polyurethane of the present invention has a water contact angle higher than 110° and excellent water repellency.

Description

technical field [0001] The invention relates to polyurethane, in particular to a fluorine-containing polyurethane obtained by addition polymerization of side chain perfluoroalkyl polyether diol and diisocyanate and a preparation method thereof, belonging to the field of polyurethane and fine chemicals. Background technique [0002] Polyurethane is a block-type polymer formed by the addition polymerization of polyether and diisocyanate, which is formed by the addition and polymerization of soft segments and hard segments. Its unique molecular structure and aggregated structure make polyurethane have excellent mechanical properties such as toughness and strength. And has superior oil resistance, wear resistance and other properties. Because of this, polyurethane has become one of the most widely used polymer materials today. However, the traditional polyurethane materials have insufficient weather resistance and water resistance. Since these polyurethanes use diisocyanates co...

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): C08G18/66C08G18/50C08G18/32C08G18/38C09D175/08C09D5/16C08G65/28
CPCC08G18/3206C08G18/3893C08G18/5015C08G65/2609C09D5/1662C09D175/08
Inventor 李战雄陈蕾遇娜刘群
Owner UPCHEM CHINA
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