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Method of preparing for anamide modified polysiloxane

A technology of amide modification and polysiloxane, which is applied in the direction of improved hand fibers, fiber treatment, textiles and papermaking, etc. It can solve the problems of different effects and easy mutual constraints, and achieve softness improvement, hydrophilicity and The effect of increasing softness and wrinkle recovery angle

Active Publication Date: 2022-08-09
常州市恒纶纺织有限公司 +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Modification with different reactive groups has different effects after finishing. Commonly used modification methods include amino modification, carboxyl modification, fatty alcohol modification, epoxy group modification, etc., but side chain polyfunctional silicone oil Various functional groups are easy to restrict each other

Method used

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  • Method of preparing for anamide modified polysiloxane
  • Method of preparing for anamide modified polysiloxane
  • Method of preparing for anamide modified polysiloxane

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0057] (1) get 0.25mol cyclohexane-1,3 diisocyanate and join in the four-necked flask that thermometer, condenser tube, magnetic stirring are housed, to wherein add 15mL acetone stirring and dissolving, stir and be warming up to 50 under nitrogen protection condition ℃, then slowly add 0.125mol double-ended aminopropyl polysiloxane SA (n=10) dropwise to it, after the addition is completed, the temperature is raised to 70 ℃, and 3 drops of dibutyltin dilaurate are added as a catalyst, and the reaction is carried out for 3h, to obtain an isocyanate group-terminated polysiloxane prepolymer;

[0058] (2) The amide-modified polysiloxane prepolymer prepared in step (1) was lowered to room temperature, 0.1 mol of succinimide was added, and the temperature was continued to rise to 80° C. for 4 hours to obtain the final product. Cool to room temperature, add water under vigorous stirring for dispersion, and obtain amide-modified polysiloxane, which is a light yellow and transparent vis...

Embodiment 2

[0062] (1) Get 0.25mol cyclohexane-1,3 diisocyanate and add it to the four-necked flask equipped with thermometer, condenser tube and magnetic stirring, add 15mL dioxane to it, stir and dissolve, stir and dissolve under nitrogen protection The temperature was raised to 50 °C, 0.125 mol SA was slowly added dropwise to it, the temperature was raised to 70 °C after the addition was completed, 3 drops of dibutyltin dilaurate were added as a catalyst, and the reaction was carried out for 3 h to obtain an isocyanate group-terminated polysiloxane prepolymer. ;

[0063] (2) Same as step (2) in Example 1, the capping ratio is calculated with reference to the method for calculating the capping ratio above, and the calculation results are shown in Table 1.

Embodiment 3

[0065] (1) get 0.25mol cyclohexane-1,3 diisocyanate and join in the four-necked flask equipped with thermometer, condenser tube, magnetic stirring, add 15mL methyl ethyl ketone to it and stir and dissolve, stir and be warming up to 50 under nitrogen protection condition ℃, slowly add 0.125mol SA dropwise thereto, and after the addition is completed, the temperature is raised to 70 ℃, 3 drops of dibutyltin dilaurate are added as a catalyst, and the reaction is carried out for 3 hours to obtain an isocyanate group-terminated polysiloxane prepolymer;

[0066] (2) Same as step (2) in Example 1, the capping ratio is calculated with reference to the method for calculating the capping ratio above, and the calculation results are shown in Table 1.

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Abstract

The invention discloses a preparation method of amide-modified polysiloxane, which belongs to the technical field of silane finishing agents. In the present invention, double-ended aminopropyl polysiloxane and isocyanate are used as raw materials, dibutyltin dilaurate (DBTDL) is used as catalyst, and the isocyanate group-terminated modified polysiloxane prepolymer is obtained by reaction, and then succinimide is used as the raw material. An amine is used as a blocking agent, and after the reaction, an isocyanate group-terminated modified polysiloxane is obtained. The organosilicon finishing agent of the block structure synthesized by the invention overcomes the mutual restriction and balance among various functional groups of the side-chain polyfunctional silicone oil, and perfectly realizes the integration of hydrophilic and soft properties. Through the exploration of catalysts, organic solvents, end-capping agents and reaction conditions, the maximum end-capping rate can reach about 90%. The wrinkle recovery angle increases, the bending length decreases, the elasticity is enhanced, and the softness performance is improved.

Description

technical field [0001] The invention relates to a preparation method of an amide-modified polysiloxane, and belongs to the technical field of silane finishing agents. Background technique [0002] Silicone finishing agent is a kind of softener with the most outstanding effect on fabric finishing. It is widely used in the textile field and has excellent performance. It can effectively impart various properties such as softness, smoothness, moisture absorption, antistatic and antibacterial to the fabric. Oxane has excellent lubricity and film-forming properties, and a thin organic silicon film is formed on the surface of the fabric fibers after finishing, which effectively prevents the fibrillation of cotton fibers and improves the fluffy and softness of the fabric, reducing the surface of the fibers. The friction coefficient improves the friction resistance between warp and weft yarns, so that the fabric has a durable soft and smooth feel. [0003] If the silicone finishing ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08G77/388D06M15/653
CPCC08G77/388D06M15/653D06M2200/20D06M2200/50
Inventor 孙恒华林伟李科徐治平梁国斌
Owner 常州市恒纶纺织有限公司