Hyperbranched polyborosiloxane containing functional groups, and preparation method thereof
A technology of hyperbranched poly and borosiloxane, which is applied in the field of polymer material modification, can solve the problems that the modification effect cannot be fully exerted, the compatibility of polyborosiloxane is poor, and the variety of polyborosiloxane is single. , to achieve the effects of excellent compatibility, easy process control and low production cost
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Embodiment 1
[0026] 1) Under stirring and nitrogen protection, first add 23.61g γ-glycidoxypropyltrimethoxysilane, 5.60g boric acid, 5.15g deionized water and 0.09g 20% tetramethylammonium hydroxide solution into three mouths After flask, reflux at 30°C for 2 hours;
[0027] 2) Under stirring and nitrogen protection, 30.89g of trimethylchlorosilane, 18.00mL of methanol and 36.00mL of pyridine were added to the solution obtained in step 1). After refluxing at 40°C for 6 hours, reduce Crude product is obtained after pressure distillation;
[0028] 3) Finally, the crude product is dissolved in 1 g of dichloromethane, the insoluble matter is filtered off, and after vacuum distillation and vacuum drying, the hyperbranched polyborosiloxane is 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 2 2 SiO 1 / 2 ] b [R 1 R 2 SiO 2 / 2 ] c [R 1 SiO 3 / 2 ] d
[0031] [R 3 2 BO 1 / 2
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 the three-necked flask, and then keep the temperature at 90°C. Reflux for 30 hours;
[0035] 2) Under stirring conditions, then add a mixed solvent consisting of 15.44g of hexamethyldisiloxane, 5.00mL of n-butanol and 8.30mL of tetrahydrofuran to the solution obtained in step 1), and reflux at 90°C for 20 hours. , The crude product is obtained after vacuum distillation;
[0036] 3) Finally, the crude product is dissolved in 1000 g of dichloromethane, the insoluble matter is filtered off, and after vacuum distillation and vacuum drying, the hyperbranched polyborosiloxane is obtained.
[0037] The prepared hyperbranched polyborosiloxane has a viscosity of 80mPa·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 2
Embodiment 3
[0042] 1) Under the conditions of stirring and nitrogen protection, 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. Reflux at 65°C for 4 hours;
[0043] 2) Under stirring and nitrogen protection, add a mixed solvent consisting of 23.22g of hexamethyldisiloxane, 20.00mL of ethanol and 10.00mL of pyridine to the solution obtained in step 1), and reflux at 65°C for 7 hours Then, the crude product is obtained after vacuum distillation;
[0044] 3) Finally, the crude product is dissolved in 50 g of toluene, the insoluble matter is filtered off, and after vacuum distillation and vacuum drying, the hyperbranched polyborosiloxane is 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 ] a [R 1 R 2 2 SiO 1 / 2 ] b [R 1 R 2 SiO 2 / 2 ] c [R 1 SiO 3 / 2 ] d
[0047] [R 3 2 BO
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