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

Fluorine water-repellent and oil-repellent agent

A water-repellent, oil-repellent, fluorine-based technology, applied in the preparation of organic compounds, carbamic acid derivatives, organic chemistry, etc., can solve problems such as monomer residues and acrylic hazards

Active Publication Date: 2014-12-10
TAIWAN FLUORO TECH
View PDF6 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The vinyl chloride / vinylidene chloride has better water resistance and good water resistance effect in textile application processing fibers, but due to the low boiling point of olefins, it often causes danger when the emulsification reaction temperature of acrylic is increased, and the latter is in the latter stage. When processing textile fibers, it often causes problems such as monomer residues

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
  • Fluorine water-repellent and oil-repellent agent
  • Fluorine water-repellent and oil-repellent agent
  • Fluorine water-repellent and oil-repellent agent

Examples

Experimental program
Comparison scheme
Effect test

Synthetic example 1

[0109] Synthesis Example 1: Fluorine-containing monomer with urethane structure (D-V1)

[0110] Place 100 grams of IPDI monomer and 0.03 grams of catalyst ES 100Ag catalyst in a three-neck round bottom bottle equipped with a mechanical stirrer, and add 55.6 grams of HEMA (2-hydroxyethyl methacrylate) into the round bottom bottle by dropwise addition, with full temperature control Below 40°C and react for 3 hours. In the second step, add 163 grams of dodecafluoroheptanol (2,2,3,3,4,4,5,5,6,6,7,7-dodecafluorooctan-1-ol) into the circle dropwise In the bottom bottle, the temperature was controlled below 40°C throughout the whole process and the reaction was carried out for 4 hours. After the reaction is completed, 318.6 grams of transparent and colorless mucus can be obtained.

[0111]

Synthetic example 2

[0112] Synthesis Example 2: Fluorine-containing monomer with urethane structure (D-V2)

[0113] Place 100 grams of IPDI monomer and 0.03 grams of catalyst ES 100Ag catalyst in a three-neck round bottom bottle equipped with a mechanical stirrer, and add 55.6 grams of 2-hydroxypropyl methacrylate into the round bottom bottle by dropwise, and the temperature control throughout the process is below 40 °C and reacted for 3 hours. In the second step, 156.6 grams of dodecafluoroheptanol (2,2,3,3,4,4,5,5,6,6,7,7-dodecafluoroheptan-1-ol) was added dropwise into the circle In the bottom bottle, the temperature was controlled below 40°C throughout the whole process and the reaction was carried out for 4 hours. After the reaction is completed, 312.2 grams of transparent and colorless mucus can be obtained.

[0114]

Synthetic example 3

[0115] Synthesis Example 3: Fluorine-containing monomer with urethane structure (D-V3)

[0116] Place 100 grams of IPDI monomer and 0.03 grams of catalyst ES 100Ag catalyst, 149.4 grams of dodecafluoroheptanol (2,2,3,3,4,4,5,5) in a three-necked round bottom bottle equipped with a mechanical stirrer , 6,6,7,7-dodecafluorooctan-1-ol) was added dropwise into the round bottom bottle, the temperature was controlled below 40°C throughout the whole process and reacted for 3 hours. In the second step, 41.2 grams of methyl ethyl ketone oxime (MEKO) was added dropwise into the round bottom bottle, and the temperature was controlled below 40°C throughout the process and reacted for 4 hours. After the reaction is completed, 290.6 grams of transparent and colorless mucus can be obtained.

[0117]

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
diameteraaaaaaaaaa
Login to View More

Abstract

The invention relates to a fluorine water-repellent and oil-repellent agent, provides a fluorine-containing copolymer, a hydroxyl-containing cationic surfactant, a polyoxyethylene ester group-containing nonionic surfactant, self-synthetic fluorine-containing polyurethane monomers, and forming a stable water-dispersible fluorine water-repellent and oil-repellent agent via an emulsion polymerization.

Description

technical field [0001] The present invention relates to a surface treatment agent, and more specifically refers to a fluorine water and oil repellent agent. Background technique [0002] Fluorine-containing compounds are often used as surface treatment agents and are widely used in the surface treatment of substrates, such as textiles, wood, metal, concrete, etc. The substrates that can show better results are textiles, which include natural fibers , Synthetic fiber and semi-synthetic fiber, the fluorine-containing compound can make the surface of the fiber hydrophobic, prevent water from adhering and reduce pollution. [0003] At present, to make fiber products have water-repellent and oil-repellent properties, fluoroalkyl acrylates are commonly used, and water-based fluorine-containing water- and oil-repellent agents obtained by emulsification and copolymerization with copolymerizable monomers. [0004] It is known that in order to improve the straight-chain perfluoroalky...

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): D06M15/277C08F220/36C08F220/18C08F220/28C08F2/30C08F2/28C08F8/00C07C271/24C07C271/60C07C269/02
Inventor 何日兴张育圣
Owner TAIWAN FLUORO 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

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com