Photosensitive discoloration self-healing smart nylon 6 and preparation method thereof
A photochromic and self-healing technology, applied in the field of photochromic self-healing intelligent nylon 6 and its preparation, nylon materials, to achieve the effects of sensitive self-healing performance, sensitive color changing performance and rich practicability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0071] 1) Weigh 1.50 g of pyrimidone derivatives, 3.1 g of hexamethylene diisocyanate, and 12 mg of dibutyltin dilaurate, and react at 70° C. for 12 hours under nitrogen atmosphere to obtain 4.1 g of diisocyanate containing ureido pyrimidone structure.
[0072] Among them, the pyrimidinone derivatives used in this example are the structural formula shown in the description formula A and the specific synthetic route disclosed in the description, and the accompanying drawings figure 1 Its data representation map is given, combined with figure 1 It can be seen that various hydrogen atoms in the molecular structural formula shown in formula A have been correspondingly characterized on the map, which also shows that the pyrimidinone derivative of this example was prepared by using the synthetic route in the specification.
[0073] 2) Weigh 0.57g of spiropyran derivative, 4.1g of diisocyanate containing ureidopyrimidinone structure, 5.1mg of dibutyltin dilaurate, 10ml of nitrogen ni...
Embodiment 2
[0078] 1) Weigh 1.80 g of pyrimidinone derivatives, 3.7 g of hexamethylene diisocyanate, and 16.7 mg of dibutyltin dilaurate, and react at 70° C. for 12 hours under nitrogen atmosphere to obtain 4.9 g of diisocyanate containing ureido pyrimidone structure.
[0079] 2) Weigh 0.67g of spiropyran derivative, 4.9g of diisocyanate containing ureidopyrimidinone structure, 7.3mg of dibutyltin dilaurate, 12ml of nitrogen nitrogen dimethylformamide, the reaction temperature is 25°C, and after 1 hour of reaction Purification waited until the product 4.5g.
[0080] 3) Weigh 40g of caprolactam, 0.44g of deionized water, and 0.4g of concentrated phosphoric acid (85wt%) into a three-necked flask, feed nitrogen to remove oxygen in the system, heat to 250°C, react for 3 hours and condense The device was changed to a vacuum device, the nitrogen gas was turned off, and the vacuum was pumped for 10 minutes at 250°C and a rotation speed of 250r / min. The melt in the three-necked flask had obvious ...
Embodiment 3
[0083] 1) Weigh 2.0 g of pyrimidone derivatives, 4.1 g of hexamethylene diisocyanate, and 20 mg of dibutyltin dilaurate, and react at 70° C. for 12 hours under nitrogen atmosphere to obtain 5.4 g of diisocyanate containing ureido pyrimidone structure.
[0084] 2) Weigh 0.75g of spiropyran derivative, 5.4g of diisocyanate containing ureidopyrimidinone structure, 8.8mg of dibutyltin dilaurate, 14ml of nitrogen nitrogen dimethylformamide, the reaction temperature is 25°C, after 1 hour of reaction Purification waited until the product 5.1 g.
[0085] 3) Weigh 40g of caprolactam, 0.44g of deionized water, and 0.4g of concentrated phosphoric acid (85wt%) into a three-necked flask, feed nitrogen to remove oxygen in the system, heat to 250°C, react for 3 hours and condense The device was changed to a vacuum device, the nitrogen gas was turned off, and the vacuum was pumped for 10 minutes at 250°C and a rotation speed of 250r / min. The melt in the three-necked flask had obvious phenomen...
PUM
Login to View More Abstract
Description
Claims
Application Information
Login to View More 


