A kind of preparation method of water-based flame-retardant self-healing polyurethane based on modified graphene
A self-healing and polyurethane technology, applied in the fields of leather finishing and fabric finishing, can solve the problems of limited service life, poor emulsion stability, and reduced content of self-healing components, so as to accelerate the self-healing process, improve the dispersion uniformity, and improve the self-healing process. The effect of repair efficiency
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Embodiment 1
[0042] Example 1: 5 g of graphene oxide was prepared into a graphene oxide aqueous dispersion (1 mg / mL) and placed in a single-necked flask containing a magnetic stirrer, and 0.231 g of hexaaminocyclotriphosphazene and 0.01 g of 4-dimethylamino Pyridine, react at room temperature under nitrogen protection for 12 hours, centrifuge and dry to obtain nitrogen-phosphorus-modified graphene oxide; disperse 5.232g nitrogen-phosphorus-modified graphene oxide in 50g methyl ethyl ketone, add 0.205g isocyanate propyltrimethoxysilane, Under the protection of nitrogen, react at 70°C for 24 hours, ultrasonically pulverize with an ultrasonic cell pulverizer at room temperature for 6 hours, and centrifugally dry to obtain nitrogen-phosphorus-silicon-modified nano-graphene oxide with a particle size of less than 100 nm; After drying at ℃ for 2 hours, take it out and place it in a desiccator to fully cool; mix 5.437g of nitrogen-phosphorus-silicon-modified nano-graphene oxide, 1g of polytetrahyd...
Embodiment 2
[0043] Example 2: 5 g of graphene oxide was prepared into a graphene oxide aqueous dispersion (1 mg / mL) and placed in a single-necked flask containing a magnetic stirrer, and 0.231 g of hexaaminocyclotriphosphazene and 0.01 g of 4-dimethylamino Pyridine, react at room temperature for 12 hours under the protection of nitrogen, centrifuge and dry to obtain nitrogen-phosphorus-modified graphene oxide; disperse 5.232g nitrogen-phosphorus-modified graphene oxide in 50g methyl ethyl ketone, add 0.247g isocyanate propyltriethoxysilane , reacted at 70°C under nitrogen protection for 24h, ultrasonically pulverized with an ultrasonic cell pulverizer at room temperature for 6h, and centrifuged and dried to obtain nitrogen-phosphorus-silicon-modified nano-graphene oxide with a particle size of less than 100nm; After drying at 110°C for 2 hours, take it out and place it in a desiccator for sufficient cooling; mix 5.479g of nitrogen-phosphorus silicon-modified nano-graphene oxide, 1g of poly...
Embodiment 3
[0044]Example 3: 5 g of graphene oxide was prepared into a graphene oxide aqueous dispersion (1 mg / mL) and placed in a single-necked flask containing a magnetic stirrer, and 0.231 g of hexaaminocyclotriphosphazene and 0.01 g of 4-dimethylamino Pyridine, react at room temperature under nitrogen protection for 12 hours, centrifuge and dry to obtain nitrogen-phosphorus-modified graphene oxide; disperse 5.232g nitrogen-phosphorus-modified graphene oxide in 50g methyl ethyl ketone, add 0.205g isocyanate propyltrimethoxysilane, Under the protection of nitrogen, react at 70°C for 24 hours, ultrasonically pulverize with an ultrasonic cell pulverizer at room temperature for 6 hours, and centrifugally dry to obtain nitrogen-phosphorus-silicon-modified nano-graphene oxide with a particle size of less than 100 nm; After drying at ℃ for 2 hours, take it out and place it in a desiccator to fully cool; mix 5.437g of nitrogen-phosphorus-silicon-modified nano-graphene oxide, 1g of polytetrahydr...
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