A phosphorus-containing fluorine-containing polyarylether/nano-hydroxyapatite composite material and its preparation method and application in dental implants
A technology of nano-hydroxyapatite and composite materials, which is applied in prosthetics, medical science, tissue regeneration, etc. It can solve the problems of new phosphorus-containing and fluorine-containing polyarylethers without patent reports, and achieve excellent biological properties and high mechanical properties. performance, excellent bioactivity and biocompatibility
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Embodiment 1
[0026] Embodiment 1: Preparation of anhydride-containing bisphenol monomer
[0027] Add 20g of phenolphthalein into a three-necked flask in an ice-acetone bath, cool to about 0°C, then slowly add 65mL of concentrated sulfuric acid that has been cooled to 0°C, and stir rapidly to make the rearrangement reaction occur; after reacting for 15 minutes, quickly filter and dry to obtain Green solid; add the reaction product and 6.0g maleic anhydride to a three-necked flask in turn, and 125mL glacial acetic acid as solvent for the next reaction; stir rapidly until all the solids are dissolved and a Diels Alder addition reaction occurs, and the color of the solution changes from reddish brown to yellow; Under the catalysis of concentrated sulfuric acid, the reaction product was rearranged, and the reaction was continued for 4 hours to complete the rearrangement reaction; filtered and dried to obtain yellow anhydride bisphenol with a yield of 40%.
Embodiment 2
[0028] Embodiment 2: Preparation of bisphenol monomer containing phosphonic acid group
[0029] Add 3.82g of anhydride-containing bisphenol and 2.08g of p-aminophenylphosphine into a three-necked flask in turn, and then add 36mL of NMP as a solvent; blow nitrogen, stir, and slowly heat to 200°C, the color of the solution changes from yellow to reddish brown, and the reaction process changes from efficient to Followed by liquid chromatography, the reaction was refluxed for 4 hours; a large amount of NMP was distilled off under reduced pressure, and vacuum-dried to obtain phosphonic acid-containing bisphenol with a yield of 80%.
Embodiment 3
[0030] Example 3: Preparation of phosphorus-containing fluorine-containing polyarylether
[0031] Add 1.8274g polyarylether containing phosphonic acid groups, 0.2017g bisphenol AF, 0.2514g difluorotriphenylphosphine, and 0.8136g difluorosulfone into a three-necked flask in turn, then add 2.50g anhydrous potassium carbonate, 20mLDMAc, and 20mL toluene; Nitrogen, raise the temperature to 145°C, make toluene and water azeotrope, remove the water in the system, and control the anhydrous and oxygen-free environment; raise the temperature to 165°C, continue to react for 8 hours until the viscosity of the polymer becomes larger; precipitate with methanol, filter out Solid; redissolve the solid in chloroform to remove inorganic salts, and filter to obtain a pure solution; volatilize and vacuum dry to obtain a polymer whose structural formula is as follows:
[0032]
[0033] Where m+n=x+y, m / n=0~1, x / y=0~1.
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