Preparation method of polydimethylsiloxane (PDMS) modified polyurethane-imides (PUI) hybrid material
A technology of polydimethylsiloxane and hybrid materials, applied in the direction of coating, etc., can solve the problems of low mechanical strength, easy to be corroded, unable to withstand high-intensity ultraviolet rays and long-term irradiation, and achieve simple and easy preparation process Easy to use, easy to industrialized production, and easy to apply in a large range
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example 1
[0021] (1) Synthesis of polydimethylsiloxane-modified poly(urethane-imide) PDMS-PUI prepolymer. Add 25.5g of isophorone diisocyanate into a 250ml three-necked flask and stir, protect with nitrogen, drop 0.2g of the toluene solution (wt=20%) of the catalyst dibutyltin dilaurate, and raise the temperature to 50°C for the catalyst dilaurate Dibutyltin was activated for 20 minutes; then 53.64g of dehydrated hydroxyalkyl-terminated polydimethylsiloxane was added dropwise to the system, reacted at 70°C for 4 hours, and a small amount was taken out for infrared spectroscopy. The disappearance of hydroxyl groups indicated that the reaction was complete. Its infrared absorption characterization data is attached figure 1 Shown: FTIR (cm-1, KBr) 2263 (v-NCO), 3323 (vN-H), 3490 (-OH), 1100, 1020 (Si-O-Si).
[0022] (2) Cool the above system to 60°C, add 6.26g of pyromellitic anhydride to the system, then add 75ml of N,N'-dimethylformamide dropwise to the system, and add 0.2g of catalyst ...
example 2
[0028] (1) Synthesis of polydimethylsiloxane-modified poly(urethane-imide) PDMS-PUI prepolymer. Add 25.5g of isophorone diisocyanate into a 250ml three-necked flask and stir, protect with nitrogen, drop 0.3g of the toluene solution (wt=20%) of the catalyst dibutyltin dilaurate, and raise the temperature to 50°C for the catalyst dilaurate Dibutyltin was activated for 20 minutes; then 53.64g of dehydrated hydroxyalkyl-terminated polydimethylsiloxane was added dropwise to the system, and after reacting at 70°C for 4 hours, a small amount was taken out to measure the infrared spectrum. The disappearance of the hydroxyl group indicated that the reaction was complete. Its infrared absorption characterization data is attached figure 1 Shown: FTIR (cm-1, KBr) 2263 (v-NCO), 3323 (vN-H), 3490 (-OH), 1100, 1020 (Si-O-Si).
[0029] (2) Lower the temperature of the above system to 50°C, add 6.26g of pyromellitic anhydride to the system, then add 75ml of N,N'-dimethylformamide dropwise to ...
example 3
[0035] (1) Synthesis of polydimethylsiloxane-modified poly(urethane-imide) PDMS-PUI prepolymer. Add 25.5g of isophorone diisocyanate into a 250ml three-necked flask and stir, protect with nitrogen, drop 0.3g of the toluene solution (wt=20%) of the catalyst dibutyltin dilaurate, and raise the temperature to 50°C for the catalyst dilaurate Dibutyltin was activated for 20 minutes; then 53.64g of polydimethylsiloxane capped with dehydrated hydroxyalkyl groups was added dropwise to the system, and after reacting at 70°C for 4 hours, a small amount was taken out to measure the infrared spectrum. The disappearance of the hydroxyl group indicated that the reaction was complete. Its infrared absorption characterization data is attached figure 1 Shown: FTIR (cm-1, KBr) 2263 (v-NCO), 3323 (vN-H), 3490 (-OH), 1100, 1020 (Si-O-Si).
[0036] (2) Cool the above system to 40°C, add 6.26g of pyromellitic anhydride to the system, then add 75ml of N,N'-dimethylformamide dropwise to the system, ...
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