A kind of hyperbranched polyborosiloxane containing functional group and preparation method thereof
A technology of hyperbranched poly and borosiloxane, applied in the field of polymer material modification, can solve the problems of inability to fully exert the modification effect, poor compatibility of polyborosiloxane, single variety of polyborosiloxane, etc. , to achieve the effects of excellent compatibility, easy process control and low production cost
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Embodiment 1
[0026]1) Under the conditions of stirring and nitrogen protection, first add 23.61g of γ-glycidoxypropyltrimethoxysilane, 5.60g of boric acid, 5.15g of deionized water and 0.09g of 20% tetramethylammonium hydroxide solution into three ports After the flask, reflux at a constant temperature of 30°C for 2 hours;
[0027] 2) Under the conditions of stirring and nitrogen protection, then add 30.89g of trimethylchlorosilane, 18.00mL of methanol and 36.00mL of pyridine into the solution obtained in step 1), and reflux at 40°C for 6 hours. Crude product was obtained after pressure distillation;
[0028] 3) Finally, after dissolving the crude product in 1 g of dichloromethane, the insoluble matter was filtered off, and after vacuum distillation and vacuum drying, the hyperbranched polyborosiloxane was obtained.
[0029] The prepared hyperbranched polyborosiloxane has a viscosity of 400mPa·s at 25°C and has the following molecular formula:
[0030] [(CH 3 ) 3 SiO 1 / 2 ] a [R 1 R ...
Embodiment 2
[0034] 1) Under stirring conditions, first add 23.61g of γ-glycidoxypropyltrimethoxysilane, 9.41g of trimethyl borate, 3.43g of deionized water and 0.04g of KOH into a three-necked flask, and keep the temperature at 90°C Reflux for 30 hours;
[0035] 2) Under stirring conditions, add 15.44g of hexamethyldisiloxane, 5.00mL of n-butanol and 8.30mL of tetrahydrofuran into the solution obtained in step 1), and reflux at 90°C for 20 hours , to obtain the crude product after distillation under reduced pressure;
[0036] 3) Finally, after dissolving the crude product in 1000 g of dichloromethane, the insoluble matter was filtered off, and after vacuum distillation and vacuum drying, the hyperbranched polyborosiloxane was obtained.
[0037] The prepared hyperbranched polyborosiloxane has a viscosity of 80 mPa·s at 25°C and has the following molecular formula:
[0038] [(CH 3 ) 3 SiO 1 / 2 ] a [R 1 R 2 2 SiO 1 / 2 ] b [R 1 R 2 SiO 2 / 2 ] c [R 1 SiO 3 / 2 ] d
[0039] [R 3 ...
Embodiment 3
[0042] 1) Under stirring and nitrogen protection conditions, first add 23.80g 3-mercaptopropyltriethoxysilane, 13.00g triethyl borate, 4.46g deionized water and 0.05g p-toluenesulfonic acid into a three-necked flask, and then Reflux at constant temperature for 4 hours at 65°C;
[0043] 2) Under the conditions of stirring and nitrogen protection, then add a mixed solvent consisting of 23.22g of hexamethyldisiloxane, 20.00mL of ethanol and 10.00mL of pyridine into the solution obtained in step 1), and reflux at 65°C for 7 hours Afterwards, crude product is obtained after distillation under reduced pressure;
[0044] 3) Finally, after dissolving the crude product in 50 g of toluene, the insoluble matter was filtered off, and after vacuum distillation and vacuum drying, the hyperbranched polyborosiloxane was obtained.
[0045] The prepared hyperbranched polyborosiloxane has a viscosity of 100 mPa·s at 25°C and has the following molecular formula:
[0046] [(CH 3 ) 3 SiO 1 / 2 ]...
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