A kind of preparation method of graphene modified waterborne polyurethane
A water-based polyurethane and graphene modification technology, which is applied in the preparation and application of new materials and functional polymer materials, can solve the problems of unreported modified water-based polyurethane, difficult large-scale industrial production, and complicated preparation processes, and achieves a combination of Tight, not easy to separate, good wrapping effect
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Embodiment 1
[0040] (1) Add 40 g of polyethylene adipate with a molecular weight of 1000 into the reaction flask, distill under reduced pressure at 100°C for 30 minutes, cool down to 60°C, add 20g of toluene diisocyanate, 0.2g of dibutyltin dilaurate, and heat up React at 70°C for 4 hours;
[0041] (2) Cool down to 60°C, add 2g of 1,4-butanediol and 2g of 2,2-dimethylolpropionic acid, raise the temperature to 70°C and react for 4 hours until the NCO content reaches the theoretical value;
[0042] (3) cooling to 40° C., and after reducing the viscosity with 10 g of acetone, add 2 g of triethylamine, and react for 30 minutes to obtain a prepolymer of water-based polyurethane;
[0043] (4) Dilute 5g graphene SE1430 with 10g isopropanol, then mix with 10g methyltrimethoxysilane, stir and react at room temperature for 30 minutes to obtain graphene modified by silane coupling agent;
[0044] (5) The prepolymer of the water-based polyurethane obtained in step 3 is added to the graphene modified ...
Embodiment 2
[0046] (1) Add 60g of polytetrahydrofuran diol with a molecular weight of 2000 into the reaction flask, distill under reduced pressure at 100°C for 30 minutes, cool down to 60°C, add 40g of hexamethylene diisocyanate and 0.5g of stannous octoate, and heat up to 90°C React for 2 hours;
[0047] (2) Cool down to 60°C, add 5g of diethylene glycol and 8g of 2,2-dimethylolbutyric acid, raise the temperature to 90°C and react for 2 hours until the NCO content reaches the theoretical value;
[0048] (3) cooling to 60° C., and after reducing the viscosity with 20 g of butanone, add 5 g of ammonia water and react for 15 minutes to obtain a prepolymer of water-based polyurethane;
[0049] (4) Dilute 20g graphene SE1231 with 20g isopropanol, then mix with 40gKH560, stir and react at room temperature for 30 minutes to obtain graphene modified by silane coupling agent;
[0050] (5) Add the prepolymer of the waterborne polyurethane obtained in step 3 to the graphene modified by the silane ...
Embodiment 3
[0052] (1) Add 40g of polypropylene glycol with a molecular weight of 2000 into the reaction flask, distill under reduced pressure at 100°C for 60 minutes, cool down to 60°C, add 30g of isophorone diisocyanate and 0.3g of dibutyltin dilaurate, and heat up to 80°C React for 2 hours;
[0053] (2) Cool down to 60°C, add 3g of neopentyl glycol and 4g of 2,2-dimethylolpropionic acid, heat up to 80°C and react for 2 hours until the NCO content reaches the theoretical value;
[0054] (3) cooling to 40° C., and after reducing the viscosity with 10 g of tetrahydrofuran, add 3 g of triethanolamine and react for 15 minutes to obtain a prepolymer of water-based polyurethane;
[0055] (4) Dilute 10g graphene G-Powder with 15g isopropanol, then mix with 20g KH570, stir and react at room temperature for 30 minutes to obtain graphene modified by silane coupling agent;
[0056] (5) The prepolymer of the aqueous polyurethane that step 3 obtains is joined in the graphene that the silane couplin...
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