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

Waterborne polyurethane resin for synthetic leather fabric and preparation method of waterborne polyurethane resin

A water-based polyurethane and synthetic leather technology, applied in the field of macromolecular polymers, can solve the problems of poor folding resistance, poor abrasion resistance, and development limitations of synthetic leather fabrics, and achieves good wear resistance, good folding resistance at room temperature, and is beneficial to Environmental and physical and mental health effects

Active Publication Date: 2017-09-08
HEFEI KETIAN WATERBORNE TECH CO LTD +1
View PDF8 Cites 12 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, due to technical restrictions on the use of water-based polyurethane resin for synthetic leather fabrics, the development of synthetic leather fabrics is limited, especially in terms of poor wear resistance and poor folding resistance.

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
  • Waterborne polyurethane resin for synthetic leather fabric and preparation method of waterborne polyurethane resin
  • Waterborne polyurethane resin for synthetic leather fabric and preparation method of waterborne polyurethane resin
  • Waterborne polyurethane resin for synthetic leather fabric and preparation method of waterborne polyurethane resin

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0045] Add 65g of polytetrahydrofuran diol, 58g of polycarbonate diol with a molecular weight of 900, 21g of polycarbonate diol with a molecular weight of 2000 and 9g of hydroxyl-terminated polysiloxane diol in a three-necked flask, and heat to 100° C. Press dehydrate for 1 hour. Then add 28.5g of toluene diisocyanate and 14.5g of diphenylmethane diisocyanate, heat up to 85°C, react for 2h, cool down to 50°C, add 7.5g of dimethylol propionic acid, 0.4g of organic bismuth catalyst and 70g of acetone, stir After uniformity, heat to 70°C, react for 6 hours, cool down to 40°C, add 9.6g γ-glycidyl etheroxypropyl trimethoxysilane, react for 10min, cool down to 5°C, add 5.2g triethylamine to neutralize, add 440g After emulsification and dispersion in ice water, 5 g of isophorone diamine and 14.4 g of ethylenediamine were added for post-chain extension, the emulsification and dispersion were continued, and then the acetone was removed by distillation under reduced pressure to obtain a...

Embodiment 2

[0047] Add 60g polytetrahydrofurfuryl ester diol, 55g polycarbonate diol with a molecular weight of 900, 26g polycarbonate diol with a molecular weight of 2000 and 8g hydroxyl-terminated polysiloxane diol in a three-necked flask, heat to 100° C. Press dehydrate for 1 hour. Then add 28.5g toluene diisocyanate and 14.5g diphenylmethane diisocyanate, heat up to 85°C, react for 2h, cool down to 50°C, add 7.5g dimethylol propionic acid, 0.4g organic bismuth catalyst and 70g acetone, stir After that, heat to 70°C, react for 6 hours, cool down to 40°C, add 9.6g of γ-glycidyl etheroxypropyl trimethoxysilane, react for 10min, cool down to 3°C, add 5.2g of triethylamine to neutralize, add 440g of ice Water emulsified dispersion, while adding 5g of isophorone diamine and 14.4g of ethylenediamine for post-chain extension, continued emulsification and dispersion, and then removed acetone by vacuum distillation to obtain a water-based polyurethane resin emulsion.

Embodiment 3

[0049] Add 64g of polytetrahydrofurfurate diol, 67g of polycarbonate diol with a molecular weight of 900, 23g of polycarbonate diol with a molecular weight of 2000 and 8g of hydroxyl-terminated polysiloxane diol in a three-necked flask, and heat to 100°C for vacuum decompression Dehydrate for 1 hour. Then add 28.5g toluene diisocyanate and 14.5g diphenylmethane diisocyanate, heat up to 85°C, react for 2h, cool down to 50°C, add 7.5g dimethylol propionic acid, 0.4g organic bismuth catalyst and 70g acetone, stir Afterwards, heat to 65-70°C, react for 6 hours, cool down to 40°C, add 9.6g of γ-glycidyl etheroxypropyl trimethoxysilane, react for 10min, cool down to 3°C, add 5.2g of triethylamine to neutralize, add 440g of ice water was emulsified and dispersed, and 5g of isophoronediamine and 14.4g of ethylenediamine were added at the same time for post-chain extension, and the emulsification and dispersion was continued. Then, acetone was removed by vacuum distillation to obtain a...

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
Breaking strengthaaaaaaaaaa
Elongation at breakaaaaaaaaaa
Login to View More

Abstract

The invention provides waterborne polyurethane resin for a synthetic leather fabric and a preparation method of the waterborne polyurethane resin. The waterborne polyurethane resin is prepared from the following raw material components in parts by weight: 20 to 50 parts of polyhydric alcohols, 5 to 20 parts of polyisocyanate, 1 to 6 parts of an anionic hydrophilic chain-extending agent, 0.05 to 0.2 part of a catalyst, 0.1 to 0.3 part of a silane coupling agent, 1 to 4 parts of a salt-forming agent and 1 to 5 parts of a second small molecule chain-extending agent, wherein the polyhydric alcohols comprise hydroxyl-terminated polysiloxanediol, polytetrahydrofuran polyol and polycarbonate diol; the weight ratio of the hydroxyl-terminated polysiloxanediol to the polytetrahydrofuran polyol to the polycarbonate diol is (2 to 6) to (10 to 25) to (18 to 30). The waterborne polyurethane resin obtained by the preparation method provided by the invention has the advantages of good alcohol resistance, good normal temperature folding resistance and good wear resistance; a production process of the preparation method provided by the invention is simple; a large amount of toxic or harmful organic solvents in the production process are avoided, so environmental protection and physical and psychological health of a human body are benefited.

Description

technical field [0001] The invention relates to the field of high molecular polymers, and specifically discloses a water-based polyurethane resin used for synthetic leather fabrics and a preparation method thereof. Background technique [0002] With the development and progress of science and technology, artificial synthetic leather has increasingly entered people's lives. At present, most of the synthetic leathers on the market still use oleoresin to make synthetic leather. A large amount of harmful organic solvents such as dimethylformamide and toluene are used in the production of oleoresin, which has caused great harm to the ecological environment and human health. As people pay more and more attention to the environment and health, the disadvantages of oily synthetic leather are unstoppably highlighted. [0003] The water-based polyurethane resin is hydrophilic by introducing hydrophilic groups, and then undergoes neutralization reaction to form a salt to make it hydr...

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
IPC IPC(8): C08G18/48C08G18/44C08G18/34C08G18/66C08G18/61C08G18/12C08G18/32C08J3/24
CPCC08G18/0823C08G18/12C08G18/348C08G18/4018C08G18/44C08G18/4854C08G18/61C08G18/6625C08J3/24C08J2375/08C08G18/3228C08G18/3234
Inventor 戴家兵詹绍文冯林林赵学庭李维虎
Owner HEFEI KETIAN WATERBORNE TECH CO LTD
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