Branched polysiloxane as well as preparation method and application thereof
A polysiloxane and siloxane technology, applied in the direction without pigment coating, can solve the problems of poor product structure controllability, and achieve the effects of uniform distribution of cross-linking points, low viscosity and high functional group degree.
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Embodiment 1
[0042] Add 45 parts of ethyl orthosilicate, 22 parts of tetramethyldisiloxane, 30 parts of tetramethyldivinyldisiloxane, and 0.1 part of trifluoromethanesulfonic acid into a three-necked flask, under nitrogen atmosphere for 70 Stir at ℃ for 3 hours, then slowly add 7.5 parts of deionized water dropwise, further hydrolysis and polycondensation for 3 hours, after the polycondensation reaction reaches equilibrium, raise the temperature to distill the ethanol generated by hydrolysis, cool down to 70 ℃ and add 0.1 parts of trifluoromethanesulfonic acid to continue the reaction 2h. After the reaction, wash with water to remove the acid and residual ethanol, etc., and then distill off the volatiles in the mixed solution under reduced pressure. The condition is 80°C / -0.09MPa / 2h, and the temperature is lowered to obtain a liquid multifunctional intermediate. The obtained product siloxane (III) has a vinyl content of 13.1% by mass and a silicon-hydrogen bond hydrogen content of 0.45% by...
Embodiment 2
[0044] Add 60 parts of phenyltriethoxysilane, 13 parts of tetramethyldisiloxane, 19 parts of tetramethyldivinyldisiloxane, and 0.1 part of trifluoromethanesulfonic acid into a three-necked flask, and in a nitrogen atmosphere, Stir at 70°C for 3 hours, then slowly add 7 parts of deionized water dropwise, further hydrolysis and polycondensation for 3 hours, after the polycondensation reaction reaches equilibrium, raise the temperature to distill the ethanol generated by hydrolysis, cool down to 70°C and add 0.1 part of trifluoromethanesulfonic acid, Continue to react for 2h. After the reaction, wash with water to remove the acid and residual ethanol, etc., and then distill off the volatiles in the mixed solution under reduced pressure. The condition is 80°C / -0.09MPa / 2h, and the temperature is lowered to obtain a liquid multifunctional intermediate. The obtained product siloxane (IV) has a mass percentage content of vinyl group of 8.68% and a silicon-hydrogen bond hydrogen mass p...
Embodiment 3
[0046] Add 54 parts of vinyltriethoxysilane, 16 parts of tetramethyldisiloxane, 22 parts of tetramethyldivinyldisiloxane, and 0.1 part of trifluoromethanesulfonic acid into a three-necked flask. Stir at 70°C for 3 hours, then slowly add 8 parts of deionized water dropwise, further hydrolysis and polycondensation for 3 hours, after the polycondensation reaction reaches equilibrium, raise the temperature to distill out the ethanol generated by hydrolysis, cool down to 70°C and add 0.1 parts of trifluoromethanesulfonic acid, Continue to react for 2h. After the reaction, wash with water to remove the acid and residual ethanol, etc., and then distill off the volatiles in the mixed solution under reduced pressure. The condition is 80°C / -0.09MPa / 2h, and the temperature is lowered to obtain a liquid multifunctional intermediate. The obtained product siloxane (IV) was measured by chemical titration with a mass percentage of vinyl groups of 23.3% and a silicon-hydrogen bond hydrogen mas...
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