Polyether polyurethane material containing phosphorylcholine group on side chain and preparation method thereof
A polyurethane material, phosphorylcholine technology, applied in the field of medical polymer materials, can solve the problems of reduced mechanical properties of materials, limited improvement of biocompatibility, complicated methods, etc., achieves high stretching ability and flexibility, and improves biological Compatibility, the effect of simple preparation process
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Embodiment 1
[0040]15g (0.01mol) Poloxamer 188 (M n =1500, PEOwt%=20%) and 8.52g (0.02mol) of HDI-BDO-HDI (dissolved in dimethyl sulfoxide: 10g / 30mL) were placed in a three-necked flask, protected by dry nitrogen, mechanically stirred, and heated to 80 ℃, after reacting for 4 hours, lower the temperature to 20℃, add 3.61g (0.01mol) DAPC, and stir. When the viscosity of the system becomes too high and cannot be stirred normally, add an appropriate amount of dichloromethane. After stirring for 1 hour, add dichloromethane to a concentration of about 15 wt%, settled with glacial ether, filtered with suction, and vacuum-dried at room temperature to constant weight to obtain phosphorylcholine-modified polyurethane P1.
[0041] Preparation of membrane material: Dissolve P1 in the organic solvent dioxane to prepare a solution with a concentration of 6.5% (g / mL), volatilize at 25°C under normal pressure for 80 hours, and then dry in vacuum at normal temperature to obtain the membrane material. The...
Embodiment 2
[0043] 15g (0.01mol) Poloxamer 188 (M n =1500, PEOwt%=20%) and 7.40g (0.02mol) BDI-BDO-BDI (dissolved in dimethyl sulfoxide: 10g / 30mL) were placed in a three-necked flask, protected by dry nitrogen, mechanically stirred, and heated to 80 ℃, after reacting for 3 hours, lower the temperature to 18℃, add 3.61g (0.01mol) DAPC, and stir. When the viscosity of the system becomes too high and cannot be stirred normally, add an appropriate amount of dichloromethane. After stirring for 1 hour, add dichloromethane to a concentration of about 15 wt%, settled with glacial ether, filtered with suction, and vacuum-dried at room temperature to constant weight to obtain phosphorylcholine-modified polyurethane P2.
[0044] Preparation of membrane material: Dissolve P2 in the organic solvent chloroform, make a solution with a concentration of 5.5% (g / mL), volatilize at 24 ° C under normal pressure for 90 hours, and then dry it in vacuum at normal temperature to obtain the membrane material. Th...
Embodiment 3
[0046] 10g (0.01mol) polypropylene oxide (PPO, M n =1000) and 8.52g (0.02mol) of HDI-BDO-HDI (dissolved in dimethyl sulfoxide: 10g / 30mL) were placed in a three-necked flask, protected by dry nitrogen, mechanically stirred, heated to 85°C, and reacted for 3 hours. Cool down to 20°C, add 3.61g (0.01mol) DAPC, and stir. When the viscosity of the system becomes too high and cannot be stirred normally, add an appropriate amount of dichloromethane. After stirring for 1.5h, add dichloromethane to a concentration of about 15wt%, ice diethyl ether Sedimentation, suction filtration, vacuum drying at room temperature to constant weight to obtain phosphorylcholine modified polyurethane P3.
[0047] Preparation of membrane material: Dissolve P3 in the organic solvent chloroform to make a solution with a concentration of 4% (g / mL), use a polytetrafluoroethylene mold to volatilize at 15°C under normal pressure for 60 hours, and take the membrane out of the mold The membrane material is obta...
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