Vinyl-terminated epoxidized polysiloxane modified multifunctional solution-polymerized styrene-butadiene rubber and preparation and application thereof
A technology of vinyl-terminated epoxy polysilane and solution-polymerized styrene-butadiene rubber, which is applied in the field of functional functionalized material preparation and achieves the effect of wide range of uses
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preparation example
[0107] Source preparation example (source example) 1
[0108] Add 100g of anhydrous vinyl polydimethylhydrogensiloxane (viscosity of 15000mPa·s, vinyl content of 0.56mol%, hydrogen content of 0.02%) into a dried 500mL four-necked flask, and dry over molecular sieves 100mL of anhydrous toluene, feed high-purity nitrogen to drive away the air in the bottle and protect the reaction system, add dropwise 2.5mL of 0.1wt% chloroplatinic acid toluene solution, control the temperature at 50°C, and then add 2.9g of allyl glycidol Add the ether into the separatory funnel and drop it into the reaction solution within 1 h, stir and react at this temperature for 5.5 h, after the reaction is over, add 100 mL of ion-free water to wash the reaction solution for 15 min, then separate the water phase at room temperature, Then vacuum removed low boilers, solvent and unreacted allyl glycidyl ether at about 90° C. to obtain light yellow transparent liquid, and the residual active hydrogen content i...
preparation example 2
[0111]Add 100 g of anhydrous vinyl polymethylvinyl hydrogen-containing siloxane (viscosity of 18000 mPa·s, vinyl content of 0.98 mol%, hydrogen content of 0.04 mol%) into a dried 500 mL four-necked flask, molecular sieve Dried anhydrous toluene 100mL, control the temperature at about 50°C. Add 4.4mL of 0.1wt% chloroplatinic acid toluene solution dropwise, feed high-purity nitrogen to drive away the air in the bottle and protect the reaction system, control the temperature at 65°C, and then Add 5.3g of allyl glycidyl ether into the separatory funnel and drop it into the reaction solution within 2h, stir and react at this temperature for 8h, after the reaction is over, add 100mL of ion-free water to wash the reaction solution for 15min, and then in The water phase was separated at room temperature, and then the low boilers, solvent and unreacted allyl glycidyl ether were removed in vacuum at about 120°C to obtain a light yellow transparent liquid, and the residual active hydrogen...
preparation example 3
[0114] Add 100g of vinyl-terminated polydiethylhydrosiloxane (viscosity of 58000mPa·s, vinyl content of 0.85mol%, hydrogen content of 0.08%), molecular sieve-dried non- Water toluene 100mL, feed high-purity nitrogen to drive away the air in the bottle and protect the reaction system, add dropwise 0.1wt% chloroplatinic acid toluene solution 4.2mL, control the temperature at 85 °C, and then add 11g of 1,2-epoxy- Add 4-vinylcyclohexane into the separatory funnel and drop it into the reaction solution within 1.5h, stir and react at this temperature for 5.5h, after the reaction is over, add 100mL ion-free water to wash the reaction solution for 15min, and then The water phase was separated at room temperature, and the low boilers, solvent and unreacted 1,2-epoxy-4-vinylcyclohexane were removed in vacuum at about 150°C to obtain a light yellow transparent liquid. As a result, the residual active hydrogen content in the pale yellow transparent liquid product was 12 mmol%.
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