A heat-resistant and flame-retardant latent curing agent for epoxy resin
A technology of latent curing agent and epoxy resin, which is applied in the field of latent curing agent and its preparation, triazine heterocyclic modified imidazole type epoxy resin latent curing agent and its preparation field, which can solve the problem of long steps and poor storage , expensive raw materials and other issues
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Embodiment 1
[0021] Dissolve 184.5g of cyanuric chloride in 500ml of tetrahydrofuran, cool to below 10°C, add 41.7g of 1-(3-aminopropyl)imidazole, and stir for 1 hour. Then 100g of 40% aqueous sodium hydroxide solution was added dropwise to neutralize the generated hydrogen chloride. The reactants were moved into a small autoclave, filled with saturated liquid ammonia, and all valves were closed. The temperature was then slowly raised to 100° C., and the reaction was continued for 2 hours. Then the pressure was released, and the product was suction filtered and washed with water to obtain a white solid. This solid was blended with 129g of cyanuric acid and 258g of water, heated to 80°C for 1 hour. After filtering and drying, a white solid was obtained, which was finally crushed into an ultrafine powder.
Embodiment 2
[0023] Dissolve 184.5 g of cyanuric chloride in 600 g of 1,4-dioxane, cool to 0-10°C, add 46.3 g of 1-(3-aminopropyl)-2-methylimidazole, and stir for 1 hour. Add 100g of 40% sodium hydroxide aqueous solution to neutralize the generated hydrogen chloride. The reactants were transferred into a small autoclave, filled with saturated liquid ammonia, and closed the valve. Slowly raise the temperature to 100°C, and continue the reaction for 2 hours. Then release the pressure, filter with suction and wash with water to obtain a white solid. This solid was blended with 129g of cyanuric acid and 258g of water, heated to 90°C for 1 hour. After filtering and drying, a white solid was obtained, which was finally crushed into an ultrafine powder.
Embodiment 3
[0025] Dissolve 184.5 g of cyanuric chloride in 650 g of n-butyl ether, cool to 10°C, add 41.7 g of 1-(2-aminoethyl)-2-methylimidazole, and react for 1 hour. The reactant was transferred into a small autoclave, and the temperature was raised while feeding liquid ammonia under high pressure to react, and finally the temperature was raised to 100°C and the high-pressure ammonia flow was maintained, and the reaction was continued for 1 hour. The n-butyl ether was distilled off under reduced pressure, and the residue was washed with water to obtain a white solid. This solid was blended with 129 g of cyanuric acid and 258 g of water and heated to reflux for 1 hour. After filtering and drying, a white solid was obtained, which was finally crushed into an ultrafine powder.
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