Preparation method of hard tissue substitute material
A hard tissue and system technology, applied in the direction of coating, etc., can solve the problems of poor bonding strength, achieve strong bonding strength, simple and easy operation, and avoid phase change and decomposition
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[0015] The present invention also provides a method for preparing a hard tissue substitute material, the method comprising the following steps:
[0016] S1. Preparation of nano-hydroxyapatite powder;
[0017] S2, substrate pretreatment;
[0018] S3. Electrophoretic deposition suspension configuration: firstly mix hydroxyapatite powder, ZnO powder and Mg(NO 3 ) 2 ·6H 2 O powder is added to isopropanol according to the mass percentage of (1-10):1:1-2, so that the total concentration of the electrophoretic deposition suspension is 6-12g / L; then after ultrasonic oscillation, magnetic stirring and aging Prepare nano-HA / ZnO electrophoretic deposition suspension; the ultrasonic oscillation power is 200W, the time is 30-60min; the magnetic stirring time is 2-5h, and the aging time is 1-3h;
[0019] S4, electrophoretic deposition treatment, pour the nano-HA / ZnO electrophoretic deposition suspension into the hydrothermal electrophoresis reactor, and the filling degree is controlled ...
Embodiment 1
[0031] 1) Use commercially available analytically pure Ca(NO 3 ) 2 4H 2 O, (NH 2 ) 2 HPO 4 , CO(NH2)2 as raw material, and synthesize nano-sized hydroxyapatite powder by chemical precipitation method. The specific process is as follows: first, the analytically pure Ca (NO 3 ) 2 4H 2 O and (NH 2 ) 2 HPO 4 Mix, add distilled water to dissolve, and ensure the Ca in the solution 2+ The ion concentration is 0.05mol / L; according to the mass ratio Ca(NO 3 ) 2 4H 2 O and (NH 2 ) 2 HPO 4 Total mass / urea=1:5 Add urea powder, and at the same time add dispersant polyethylene glycol, the amount of polyethylene glycol added is 3% of the total mass, then stir rapidly to fully react, and keep the reaction temperature at 50°C; Pay attention to sealing the container to prevent the volatilization of ammonia gas; put it into a water bath after fully stirring for 2 hours, and age at 50°C for 12 hours; filter and wash the suspension, first wash it with distilled water for 3 times, ...
Embodiment 2
[0036] 1) Use commercially available analytically pure Ca(NO 3 ) 2 4H 2 O, (NH 2 ) 2 HPO 4 , CO(NH2)2 as raw material, and synthesize nano-sized hydroxyapatite powder by chemical precipitation method. The specific process is as follows: first, the analytically pure Ca (NO 3 ) 2 4H 2 O and (NH 2 ) 2 HPO 4 Mix, add distilled water to dissolve, and ensure the Ca in the solution 2+ The ion concentration is 0.4mol / L; according to the mass ratio Ca(NO 3 ) 2 4H 2 O and (NH 2 ) 2 HPO 4 Total mass / urea=1:10 Add urea powder and dispersant polyethylene glycol at the same time. The amount of polyethylene glycol added is 3% of the total mass, and then stir rapidly to fully react, and the reaction temperature is kept at 60°C; Pay attention to sealing the container to prevent the volatilization of ammonia gas; put it into a water bath after fully stirring for 2 hours, and age at 50°C for 12 hours; filter and wash the suspension, first wash it with distilled water for 3 times...
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