Calcium phosphate composite powder and preparing method thereof
A composite powder and calcium phosphate technology, which is applied in the treatment of dyed polymer organic compounds and fibrous fillers, can solve the problems of inability to obtain implant effects, the degradation rate of tricalcium phosphate affecting the osseointegration ability of implants, and low solubility , to achieve the effect of easy preparation process conditions, low cost and uniform particle size distribution
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Embodiment 1
[0012] A certain proportion of polyethylene glycol (PEG) and CaCl 2 (PEG:CaCl 2 =3:1, molar ratio, the polymer is calculated by the number of moles of structural units, the same below) is dissolved in 200ml of distilled water, Na 3 PO 4 12H 2 O was dissolved in 100ml of distilled water, the molar ratio of Ca / P was 1.60, stirred and dissolved, and placed in refrigeration at 5°C. After the temperature stabilized, the two solutions were mixed at 5° C., adjusted to pH 10 with ammonia water, and reacted for 30 minutes under magnetic stirring. The precipitate was suction filtered, washed, and freeze-dried for 48 hours to obtain a calcium phosphate precursor. The calcium phosphate precursor is raised to 800°C at a heating rate of 10°C / min for 3 hours, and then lowered to room temperature with the furnace, and the content of hydroxyapatite is 60%, and the content of α-phase tricalcium phosphate is 40%. calcium phosphate composite powder.
Embodiment 2
[0014] A certain proportion of polyvinyl alcohol (PVA) and CaCl 2 (PVA: CaCl 2 =3:1, molar ratio) was dissolved in 200ml of distilled water, Na 3 PO 4 12H 2 O was dissolved in 100ml of distilled water, reacted at 50°C, the Ca / P molar ratio was 1.60, the pH was adjusted to 10 with ammonia water, and reacted for 30 minutes under magnetic stirring. The precipitate was suction filtered, washed, and freeze-dried for 48 hours to obtain a calcium phosphate precursor. The calcium phosphate precursor is raised to 800°C at a heating rate of 10°C / min for 3 hours, and then lowered to room temperature with the furnace, and the content of hydroxyapatite is 60%, and the content of β-phase tricalcium phosphate is 40%. calcium phosphate composite powder.
Embodiment 3
[0016] A certain proportion of PEG and CaCl 2 (PEG:CaCl 2 =3:1, molar ratio) was dissolved in 200ml of distilled water, Na 3 PO 4 12H 2 O was dissolved in 100ml of distilled water, the Ca / P molar ratio was 1.50, stirred and dissolved, and placed in a refrigerator at 5°C. After the temperature stabilized, the two solutions were mixed at 5° C., adjusted to pH 9 with ammonia water, and reacted for 30 minutes under magnetic stirring. The precipitate was suction filtered, washed, and freeze-dried for 48 hours to obtain a calcium phosphate precursor. The calcium phosphate precursor is raised to 800°C at a heating rate of 10°C / min and kept at 800°C for 3 hours, and then lowered to room temperature with the furnace, and the content of β-phase tricalcium phosphate is 50%, and the content of α-phase tricalcium phosphate is 50%. % calcium phosphate composite powder.
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