Polyurethane elastomer and application thereof
A technology of polyurethane elastomer and polyurethane prepolymer, which is applied in the direction of prosthesis, drug delivery, tissue regeneration, etc., can solve the problem of affecting the light transmittance and refractive index of the intraocular lens, unable to cooperate with the physiological refraction adjustment function of the eye, and not satisfying the actual situation Use requirements and other issues to achieve effects that are not conducive to cell proliferation and protein adhesion, non-toxic and immunogenic, and good optical properties
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[0029] The application also provides a method for preparing a polyurethane elastomer, which specifically includes the following steps:
[0030] The polyester diol and isophorone diisocyanate are reacted under a catalyst to stabilize the NCO value to obtain a polyurethane prepolymer;
[0031] The polyurethane prepolymer is reacted with the small molecule chain extender and the end-capping agent under the catalyst, and the polyurethane elastomer is obtained after curing.
[0032] In the above preparation process, the application first reacts polyester diol and isophorone diisocyanate under a catalyst to a stable NCO value to obtain a polyurethane prepolymer; in this process, the catalyst is specifically selected from bismuth isooctoate, Potassium isooctanoate, stannous octoate, dibutyltin dilaurate, 1,8-diazabicyclo[5.4.0]undec-7-ene, 1,4-dimethylpiperazine, triethylenedicarbonate One or more of amine, bis(dimethylaminoethyl) ether, dimethylcyclohexylamine and pentamethyldiethy...
Embodiment 1
[0037] Under nitrogen protection, add 10.57g of isophorone diisocyanate to 50.00g of anhydrous poly(1,6-hexanediol neopentyl adipate diol) diol (molecular weight 1500), stir evenly, then 0.10g of dibutyltin dilaurate was added to it, and the reaction was stirred at 75°C until the NCO value was stable to obtain a polyurethane prepolymer; 50.00g of the polyurethane prepolymer was taken out, defoamed at 80°C for 30min, and then 0.31g of 2-ethyl-1,3-hexanediol, 4.25g of 3-aminopropyltriethoxysilane and 0.05g of dibutyltin dilaurate were mechanically stirred at 1000rpm for 10min. After curing Obtained transparent polyurethane elastomer material (such as figure 1 ).
Embodiment 2
[0039] Under nitrogen protection, add 10.57g of isophorone diisocyanate to 50.00g of anhydrous poly(1,6-hexanediol neopentyl adipate diol) diol (molecular weight 1500), stir evenly, then 0.20 g of dibutyltin dilaurate was added thereto, and the reaction was stirred at 75° C. until the NCO value was stable to obtain a polyurethane prepolymer. Take out 50.00g of polyurethane prepolymer, defoaming under vacuum at 70°C for 45min, then add 3.65g of 2-ethyl-1,3-hexanediol to it, stir mechanically, rotate speed at 1200rpm for 10min, vacuum at 40°C The transparent polyurethane elastomer material was obtained by curing after defoaming for 6 hours.
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