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Preparation method of high-strength self-repairing polyurethane

A self-healing and operating method technology, applied in the field of smart materials, can solve problems such as shortening the service life of materials, decreasing mechanical properties and stability, and difficult to observe cracks

Inactive Publication Date: 2021-07-30
BEIJING UNIV OF CHEM TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, when the material has been used for a long time, a large number of cracks will be generated inside and on the surface. These cracks will greatly reduce the mechanical properties and stability of the material and shorten the service life of the material.
External cracks can be repaired by methods such as welding and cementing, but internal cracks are difficult for us to observe, so we need to find new repair methods

Method used

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  • Preparation method of high-strength self-repairing polyurethane
  • Preparation method of high-strength self-repairing polyurethane
  • Preparation method of high-strength self-repairing polyurethane

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] Weigh 5g of polypropylene glycol and 1.785g of small molecule chain extender containing furan group in a three-necked flask, then add 2.94g of liquefied MDI, catalyst dibutyltin dilaurate and a little solvent tetrahydrofuran, place the three-necked flask in an oil bath pot The magnetic stirring was turned on, nitrogen was introduced, and the temperature was slowly raised to 60 °C for 5 h. After 5 hours, 0.896 g of bismaleimide was dissolved in THF and injected into the three-necked flask with a syringe, and the reaction was continued at 60° C. for 24 hours. After the reaction is completed, turn off the heating and stop stirring, pour the mixed liquid into a polytetrafluoroethylene mold, place the product in a fume hood for 72 hours to evaporate most of the solvent, and then dry it in a vacuum oven at 60°C for 24 hours to obtain a polyurethane dry film PU-DA-1. The sample was cut into a dumbbell shape, cut from the middle, placed at 120°C for 40min, and at 60°C for 24h ...

Embodiment 2

[0026] Weigh 4g of polypropylene glycol and 2.142g of small molecule chain extender containing furan group in a three-necked flask, then add 2.94g of liquefied MDI, catalyst dibutyltin dilaurate and a little solvent tetrahydrofuran, place the three-necked flask in an oil bath pot The magnetic stirring was turned on, nitrogen was introduced, and the temperature was slowly raised to 60 °C for 5 h. After 5 hours, 1.075 g of bismaleimide was dissolved in THF and injected into the three-necked flask with a syringe, and the reaction was continued at 60° C. for 24 hours. After the reaction is completed, turn off the heating and stop stirring, pour the mixed liquid into a polytetrafluoroethylene mold, place the product in a fume hood for 72 hours to evaporate most of the solvent, and then dry it in a vacuum oven at 60°C for 24 hours to obtain a polyurethane dry film PU-DA-1.5. The sample was cut into a dumbbell shape, cut from the middle, placed at 120°C for 40min, and at 60°C for 24...

Embodiment 3

[0028] Weigh 3.333g of polypropylene glycol and 2.380g of small molecule chain extender containing furan group in a three-necked flask, then add 2.94g of liquefied MDI, catalyst dibutyltin dilaurate and a little solvent tetrahydrofuran, place the three-necked flask in an oil bath pot Magnetic stirring was turned on in the medium, nitrogen was introduced, and the temperature was slowly raised to 60 °C for 5 h. After 5 hours, 1.195 g of bismaleimide was dissolved in THF and injected into the three-necked flask with a syringe, and the reaction was continued at 60° C. for 24 hours. After the reaction is completed, turn off the heating and stop stirring, pour the mixed liquid into a polytetrafluoroethylene mold, place the product in a fume hood for 72 hours to evaporate most of the solvent, and then dry it in a vacuum oven at 60°C for 24 hours to obtain a polyurethane dry film PU-DA-2. The sample was cut into a dumbbell shape, cut from the middle, placed at 120°C for 40min, and at...

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Abstract

The invention provides a method for preparing self-repairing polyurethane by utilizing a Diels-Alder reaction. The method comprises the following steps of: preparing self-repairing polyurethane. The preparation method is mainly characterized in that: a small molecule chain extender containing a furan group is synthesized, liquefied MDI containing a small amount of trifunctional isocyanate groups is selected as a hard segment, soft segments and the chain extender in different molar ratios are selected, a micro-crosslinking system with the isocyanate groups as crosslinking points is prepared firstly, a DA reaction group is introduced, a double-crosslinking-point network with carbamate groups and thermal reversible bonds as crosslinking points is obtained, and a series of different liquefied MDI type self-repairing polyurethanes are prepared. The method is simple to operate, and the prepared sample has the characteristics of strong mechanical properties and high repair and recovery efficiency.

Description

technical field [0001] The invention relates to a preparation method for preparing high-strength self-repairing polyurethane based on a two-step cross-linking method and utilizing Diels-Alder reaction, and belongs to the field of intelligent materials. Background technique [0002] Polymer materials are widely used in aviation, military, transportation and other fields because of their good processing performance and high mechanical strength. However, when the material has been used for a long time, a large number of cracks will occur inside and on the surface. These cracks will greatly reduce the mechanical properties and stability of the material and shorten the service life of the material. External cracks can be repaired by methods such as welding and cementing, but internal cracks are difficult to observe, so we need to find new repair methods. [0003] Inspired by the self-healing and self-diagnosis of organisms, in the mid-1980s, the scientific research community fir...

Claims

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Application Information

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IPC IPC(8): C08G18/66C08G18/48C08G18/32C08G18/83
CPCC08G18/6688C08G18/48C08G18/3275C08G18/833
Inventor 李齐方吴庚芮周政
Owner BEIJING UNIV OF CHEM TECH