A kind of method for preparing polyurethane-polyisocyanurate film gradient material
A technology of polyisocyanurate and gradient materials, which is applied in the field of preparing polyurethane-polyisocyanurate film gradient materials, can solve the problems of inability to change the elastic modulus and inability to eliminate the viscoelasticity of the rubber-plastic transition region, and achieve Good thermal stability and dielectric properties, the effect of extending the performance range
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Embodiment 1
[0033]Add 85.00g (0.05mol) of tetrahydrofuran-propylene oxide copolyether diol (PF-OP-151700) into a 500ml three-necked flask, stir and raise the temperature to 105°C, dehydrate in vacuum at -0.1MPa for 2h, wait until the temperature drops to At about 60°C, add 17.40g (0.1mol) of 2,4-toluene diisocyanate (2,4-TDI) into the three-necked flask, after natural reaction for 40min, slowly raise the temperature to 80°C to continue the reaction for 1h, add 0.05g (0.05wt% of tetrahydrofuran-propylene oxide copolyether glycol quality) dibutyltin dilaurate catalyst continued to react for 1.5 hours, and then obtained 102.4g terminal NCO-based polyurethane prepolymers to above-mentioned mixed system vacuum defoaming;
[0034] Add the anhydrous acetone of 81.92g (80wt%) in the above-mentioned prepolymer and fully stir to reduce the viscosity of the system, then add 1.54g (1.5%) of the Sudan Blue G catalyst in the presence of cyclotrimerization, and this process time is 2 hours , so that a p...
Embodiment 2
[0038] Add 85.00g (0.05mol) of tetrahydrofuran-propylene oxide copolyether diol (PF-OP-151700) into a 500ml three-necked flask, stir and heat up to 100°C, vacuum dehydrate at -0.3MPa for 2h, wait until the temperature drops to At about 50°C, add 17.40g (0.1mol) of 2,4-toluene diisocyanate (2,4-TDI) into the three-necked flask, after natural reaction for 40min, slowly raise the temperature to 85°C to continue the reaction for 1h, add 0.05g (0.05wt%) dibutyltin dilaurate catalyst continued to react for 1.5 hours, and then the above-mentioned mixed system was vacuumed and defoamed to obtain the NCO-terminated polyurethane prepolymer.
[0039] Add 81.92g (80wt%) of anhydrous acetone in the above-mentioned prepolymer and fully stir to reduce the viscosity of the system, then add 5.12g (5wt% of the prepolymer quality) 2,4-TDI, add 1.62g ( The Sudan Blue G of 1.5%), cyclotrimerization reaction takes place in the presence of catalyst, and this process time is 2 hours, pours again on a...
Embodiment 3
[0043] Add 85.00g (0.05mol) of tetrahydrofuran-propylene oxide copolyether diol (PF-OP-151700) into a 500ml three-necked flask, stir and raise the temperature to 105°C, dehydrate in vacuum at -0.1MPa for 2h, wait until the temperature drops to At about 55°C, add 17.40g (0.1mol) of 2,4-toluene diisocyanate (2,4-TDI) into the three-necked flask, after natural reaction for 40min, slowly raise the temperature to 80°C to continue the reaction for 1h, add 0.1g (0.1wt%) dibutyltin dilaurate catalyst continued to react for 2 hours, and then vacuumize and defoam the above mixed system to obtain NCO-terminated polyurethane prepolymer.
[0044] Add 61.44g (60wt%) of anhydrous acetone in the above-mentioned prepolymer and fully stir to reduce the viscosity of the system, then add 10.24g (10wt% of the prepolymer quality) 2,4-TDI, add 1.72g ( 1.5%) of Sudan Blue G, the system undergoes a cyclotrimerization reaction in the presence of a catalyst. This process takes 1 hour, and then cast on a...
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