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

Multi-block polyether type macromolecular surfactant as well as preparation method and application thereof

A technology of surfactant and block polyether, which is applied in chemical instruments and methods, dyeing methods, textiles and papermaking, etc., can solve the problems of disordered detonation, accelerated reaction speed, temperature rise, etc., and achieves the goal of reducing detonation The effect of risk, smooth reactivity, and good dispersion effect

Active Publication Date: 2021-11-12
常熟耐素生物材料科技有限公司
View PDF10 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The existing traditional polyether surfactants are all linear polyether surfactants formed by block polymerization or mixed polymerization of an initiator with active hydrogen and 1,2-alkylene oxide, and its molecular structure is relatively Simpler, polyether-type surfactants belonging to alkyl blocks, no aromatic groups in the molecule, and weak intermolecular interaction with the aromatic groups of organic dyes or pigments, so the dispersion effect on organic dyes or pigments is relatively weak Poor, and when used for anti-staining washing of denim fabrics, it will reduce the elasticity and quality of denim fabrics, and the anti-staining effect is average
[0005] In addition, it can be seen from the chemical reaction kinetics that the reaction temperature can be increased greatly, and the reaction speed can be greatly accelerated, and the ring-opening reaction of epoxy compound and hydroxyl group is an exothermic reaction. The higher the temperature, the faster the reaction speed and the greater the heat release, resulting in As the temperature rises further, the reaction speed is further accelerated. At a higher temperature, the by-products in the preparation process of polyether surfactants are more, which even leads to the risk of uncontrollable disordered detonation in the entire reaction, and the target cannot be obtained. products; and because of the rigidity of the aromatic ring, the viscosity of the epoxy compounds of aromatic-based epoxy compounds is very high. During the reaction process, the heat of reaction is very difficult to remove, the temperature is difficult to control, and disordered detonation reactions are prone to occur. The industry is still There is no technical solution that can effectively avoid the detonation reaction

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
  • Multi-block polyether type macromolecular surfactant as well as preparation method and application thereof
  • Multi-block polyether type macromolecular surfactant as well as preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0083] The present invention also discloses a preparation method of the surfactant of the above molecular structural formula (1), comprising the following steps:

[0084] (1) Add the monofunctional raw material with a single active hydrogen and the bifunctional raw material with two active hydrogens into the high-pressure alkoxylation reactor at a molar ratio of 1:0.5 to 10, and then put them into the The catalyst I containing 0.02-1% of the total mass of monofunctional raw materials and bifunctional raw materials is heated to 70-130°C and vacuumed for 30-90 minutes to remove the generated water or small organic molecules, so that the raw materials in the reactor contain The amount of water is less than 0.1% of the raw material mass, and the reaction system is replaced with nitrogen, so that the oxygen content in the reactor is lower than 500ppm. After the nitrogen replacement is completed, 1,2-epoxyalkylene compounds are introduced to carry out multi-stage block or mixed poly...

Embodiment 1

[0104] Put 150 grams (about 0.5mol) cardanol, 142 grams (about 0.45mol) cardol, 16.5 grams (about 0.05mol) methyl cardol into the autoclave, then add 1.54 grams of potassium hydroxide powder, Raise the temperature to 110°C for dehydration for 60 minutes, take a sample to detect that the moisture in the material is less than 0.1%; replace the nitrogen, and after the oxygen content in the kettle is lower than 500ppm, continue to add 264 grams (about 6mol) of ethylene oxide, and control the reaction temperature at 155- Between 165°C, the introduction of ethylene oxide is completed; then continue to add 261 grams (about 4.5mol) of propylene oxide, control the reaction temperature at 125-135°C, and the introduction of propylene oxide is completed; then continue to add 792 grams (about 18mol) ) Ethylene oxide, control the reaction temperature at 155-165°C, after the ethylene oxide is thrown in, keep warm at 120-165°C, and mature for 2 hours to ensure that the terminal of the generate...

Embodiment 2

[0111]Put 150 grams (about 0.5mol) of cardanol, 142 grams (about 0.45mol) of cardol, and 16.5 grams (about 0.05mol) of 2-methylcardol into the autoclave, and then add 4.9 grams of 30% methanol Sodium methanol solution, heated to 100°C for 60 minutes to demethanol, sampling and testing the moisture in the material is less than 0.1%. Replace nitrogen, after the oxygen content in the kettle is lower than 500ppm, continue to add 2640 grams (about 60mol) of ethylene oxide, control the reaction temperature at 155-165°C, after the introduction of ethylene oxide is complete, keep warm at 120-165°C, and mature for 30 minutes , until the reactor pressure no longer changes, that is, the unreacted ethylene oxide is basically exhausted. Lower the temperature to 100°C, vacuumize and degas for 0.5 hours to remove unreacted ethylene oxide and other non-condensable gases. Cool down to 80°C, add 1.63 g of acetic acid, and stir for 30 minutes. Transfer the above reaction product to a polymeriz...

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
Login to View More

Abstract

The invention discloses a multi-block polyether type macromolecular surfactant as well as a preparation method and application thereof. The macromolecular surfactant is obtained by carrying out alkoxylation reaction and ring-opening polymerization reaction on a monofunctional raw material and a bifunctional raw material, and can be used as an anti-staining agent for denim fabrics. According to the invention, monofunctional polyether is used as an end-capping reagent, a completely-terminated alcohol ether inert solvent I and a Lewis acid catalyst are used to form a complex, and the alcohol ether inert solvent I is added, so that the molecular weight is regulated and controlled in the synthesis process, the temperature of the whole reaction system is effectively controlled, and reaction implosion is prevented; the molecular structure of the prepared macromolecular surfactant is rich in aromatic ring structures, so that the macromolecular surfactant is easier to generate intermolecular acting force with aromatic groups of organic dyes or pigments and is easier to adsorb on the surfaces of the organic dyes or the pigments, and therefore, the macromolecular surfactant has a better dispersion effect on the organic dyes or the pigments.

Description

technical field [0001] The invention relates to the technical field of surfactant preparation, in particular to a multi-block polyether polymer surfactant and its preparation method and application. Background technique [0002] The relative molecular weight of common surfactants is about several hundred, and the carbon number of lipophilic group is 10-18, also known as low-molecular surfactants. When the relative molecular mass increases to a certain extent, it is called a polymer surfactant. But there is no clear boundary between the two, and those with a relative molecular mass above 2000 are customarily called polymer surfactants. [0003] In 1951, Strass synthesized polymer surfactant for the first time. In 1954, the first synthetic polymer surfactant (trade name Pluronics, also known as Poloxamer, Pluronic, Pluronic) was commercialized as an industrial detergent. Since then, various artificially synthesized polymer surfactants have been successively developed and app...

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): C08G65/28D06P5/12B01F17/52B01F17/42C09B67/46C09K23/42C09K23/52
CPCD06P5/12C08G65/2612C08G65/2696C09B67/009
Inventor 顾斌王震戴志成蔡秀刚
Owner 常熟耐素生物材料科技有限公司
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