Medical instrument with slidable coating layer, and syringe
A technology of medical appliances and covering layers, which is applied in the field of medical appliances, can solve the problems of liquid medicine deterioration, difficult prefilling, etc., and achieve the effect of forming good and good sliding properties
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Embodiment 1
[0103] (ingredient 1a)
[0104] 43g of 1,5-divinyl-3,3-bis[(vinyldimethylsilyl)oxy]-1,1,5,5-tetramethylpentanetrisiloxane, octamethyl 445 g of cyclotetrasiloxane and 1.5 g of trifluoromethanesulfonic acid were weighed into a 1 L eggplant-shaped flask, and reacted at 80° C. for 6 hours while stirring. The reaction product was returned to room temperature, 1.2 g of calcium carbonate was added and stirred for 3 hours, the calcium carbonate was removed by filtration to complete the polymerization, and the reaction product was removed under reduced pressure (3 kPa) at 150° C. for 2 hours. Polysiloxane with a branched structure is obtained through polymerization. The obtained polysiloxane had a viscosity of 53 mPa·s and a vinyl content of 2.2 wt%. The resulting product was used as component 1a.
[0105] (ingredient 1b)
[0106] Polymethylhydrogensiloxane (100 mol % of hydrogen groups bonded to silicon atoms, viscosity of 30 mPa·s, molecular weight of 2,100) having trimethylsilyl...
Embodiment 2
[0114] (ingredient 1a)
[0115] 22g of 1,5-divinyl-3,3-bis[(vinyldimethylsilyl)oxy]-1,1,5,5-tetramethylpentanetrisiloxane, octamethyl 593 g of cyclotetrasiloxane and 1.5 g of trifluoromethanesulfonic acid were weighed into a 1 L eggplant-shaped flask, and reacted at 80° C. for 6 hours while stirring. The reaction product was returned to room temperature, 1.2 g of calcium carbonate was added and stirred for 3 hours, the calcium carbonate was removed by filtration to complete the polymerization, and the reaction product was removed under reduced pressure (3 kPa) at 150° C. for 2 hours. Polysiloxane with a branched structure is obtained through polymerization. The obtained polysiloxane had a viscosity of 168 mPa·s and a vinyl content of 0.9 wt%. The resulting product was used as component 1a.
[0116] (ingredient 1b)
[0117] Using a methylhydrogensiloxane-dimethylsiloxane copolymer with trimethylsilyl groups at both ends (content of hydrogen groups bonded to silicon atoms: 3...
Embodiment 3
[0125] (ingredient 1a)
[0126] 43g of 1,5-divinyl-3,3-bis[(vinyldimethylsilyl)oxy]-1,1,5,5-tetramethylpentanetrisiloxane, 1,3 , 18g of 5,7-tetravinyltetramethylcyclotetrasiloxane, 445g of octamethylcyclotetrasiloxane, and 1.5g of trifluoromethanesulfonic acid were weighed into a 1L eggplant-shaped flask, and carried out at 80°C under stirring for 6 hour response. The reaction product was returned to room temperature, 1.2 g of calcium carbonate was added and stirred for 3 hours, the calcium carbonate was removed by filtration to complete the polymerization, and the reaction product was removed under reduced pressure (3 kPa) at 150° C. for 2 hours. Polysiloxane with a branched structure is obtained through polymerization. The obtained polysiloxane had a viscosity of 136 mPa·s and a vinyl content of 3.2 wt%. The resulting product was used as component 1a.
[0127] (ingredient 1b)
[0128] Polymethylhydrogensiloxane (100 mol % of hydrogen groups bonded to silicon atoms, visc...
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