TW202019817A - Sphere hydroxyapatite and method for producing the same - Google Patents

Abstract

The present invention provides a method for producing a sphere hydroxyapatite. A calcium chloride aqueous solution and an ammonium dihydrogen phosphate aqueous solution are firstly mixed uniformly. After filteration, a hydroxyapatite precipitate is obtained. The precipitate is directly dispersed into a deionized water rather than being subjected to a washing process, thereby obtaing a hydroxyapatite suspension. Next, the hydroxyapatite suspension is mixed with an alginate aqueous solution to form a slurry. And then, the slurry is dropped into a solution containing polyvalent metal cations to subject the as-drop hydroxyapatite to be solidified as gel spheres. After drying and roasting, the sphere hydroxyapatite of the present invention is produced. The method of the present invention is simple and the sphere hydroxyapatite has excellent sphericity and high intensity. Furthermore, the sphere hydroxyapatite can be applied in fileds of catalysis, adsorption separation and bioengineering. Therefore, the sphere hydroxyapatite has wider application prospect.

Description

Spherical hydroxyapatite and its forming method

The invention belongs to the field of porous material preparation, and in particular relates to a method for forming spherical hydroxyapatite.

Hydroxyapatite (hydroxyapatite, HAP) is the main inorganic component of animal bones and has excellent biocompatibility and bioactivity. At the same time, hydroxyapatite has unique ion exchange properties, and the anion and cation positions in its structure can be replaced by other ions. At the same time, during the formation of hydroxyapatite, Ca ²⁺ deficient form can also be formed, forming non-stoichiometric hydroxyapatite (Ca/P=1.4~1.67), thereby adjusting the surface acidity and alkalinity of hydroxyapatite. The structure of hydroxyapatite is stable, and it can still maintain a perfect HAP structure after calcination at 1200℃. In addition, hydroxyapatite also has a strong adsorption capacity. It is precisely because of these characteristics that hydroxyapatite has emerged in the field of catalysis and adsorption as a new type of hydroxyapatite-based catalytic and adsorption material. Hydroxyapatite itself is very brittle, not easy to form, and slightly soluble in water. At present, there are few reports on the formation of hydroxyapatite, which limits its application to a large extent.

Alginic acid is a by-product of the extraction of iodine and mannitol from brown algae kelp or Sargassum. Its molecules are composed of β-D-tetra mannuronic acid tetrasodium salt and α-L-paleo Glucuronic acid (α-L-guluronic, G) is formed by pressing (1→4) bond. When cations such as Ca ²⁺ and Ba ²⁺ are present, the Na ⁺ plasma on the carboxylate undergoes an ion exchange reaction with the multivalent cation to form a cross-linked network structure, thereby forming a hydrogel. The pellets formed from pure alginate are brittle, have low mechanical strength, and are easy to swell and cannot be used dry.

Alginate has unique properties, that is, sol-gel transformation can occur in the presence of multivalent metal cations, such as Ca ²⁺ . Therefore, the addition of alginate to hydroxyapatite assists in molding, which can greatly Improve the mechanical strength of the ball, and the preparation process is safe and simple.

The purpose of the present invention is to provide a method for forming spherical hydroxyapatite assisted by sodium alginate in view of the above technical problems and the prior art. The hydroxyapatite precipitate is prepared by the precipitation method, and then the hydroxyapatite precipitate is dissolved in water and dispersed to obtain a suspension. The alginate aqueous solution and the hydroxyapatite suspension are mixed to form a slurry, and then the slurry is dropped into In a solution containing polyvalent metal ions, hydroxyapatite solidifies into a gel ball, and after drying and roasting, spherical hydroxyapatite can be obtained.

The object of the present invention can be achieved by the following technical solutions.

A method for preparing a spherical hydroxyapatite molding method, the specific steps are: (1) Dispose calcium chloride and ammonium dihydrogen phosphate into an aqueous solution, stir and mix the two according to the molar ratio Ca/P=1.67, and mix In the process of adding ammonia to adjust pH value to 10-12; continue at 80-100°C, stirring for 1-4 hours, then let stand for aging, aging time is 10-24 hours; after filtration, a precipitate is obtained, and the precipitate is directly dispersed into deionized water To obtain a hydroxyapatite suspension; (2) the hydroxyapatite and soluble alginate aqueous solution are thoroughly mixed to make a floating slurry; (3) the mixed floating slurry is dropped into multivalent In the solution of metal cation salt, to form gel beads; (4) The gel beads are aged and taken out, washed with deionized water, and dried and roasted to prepare spherical hydroxyapatite.

The molar concentration of Ca ²⁺ in the calcium chloride aqueous solution in the above step (1) is 0.1-0.5mol/L; the molar concentration of PO ₄ ^3- in the aqueous solution of ammonium dihydrogen phosphate is 0.05-0.3mol/L; chlorine Calcium chloride and ammonium dihydrogen phosphate are mixed according to the molar ratio of Ca/P=1.67; the soluble alginate in the above step (2) is sodium alginate, potassium alginate, ammonium alginate, lithium alginate or magnesium alginate One or more than two.

The mass concentration of soluble alginate in the floating slurry in the above step (2) is 0.05% to 4%.

The mass percentage concentration of the hydroxyapatite in the floating slurry in the above step (2) is 0.5% to 25%.

The polyvalent metal cation in the above step (3) is one or more of calcium, strontium, barium, iron, cobalt, nickel, manganese, copper, zinc, or aluminum.

The concentration of the polyvalent metal cation salt in the above step (3) is 0.01 to 3 mol/L.

The aging time of the gel beads in the above step (4) is 0.1 to 24 hours.

In the above step (4), the drying temperature of the gel pellet is 20 to 150°C, and the time is 0.5 to 48 hours.

In the above step (4), the calcination temperature of the gel beads is 300 to 800°C, and the time is 0.2 to 48 hours.

The hydroxyapatite beads prepared by the above method, with a diameter of 1-5mm, can be used in the fields of catalysis, adsorption separation and bioengineering.

The advantage of the invention is that the precipitate in the preparation process of hydroxyapatite does not need to be washed after being filtered, and is directly dissolved in deionized water to prepare a suspension. Because the impurities in the filter cake are mainly ammonia and ammonium chloride, they can be directly volatilized during the subsequent heating and roasting treatment. Therefore, when the amount of precipitation is relatively large, the filter cake is thick and the filtration is very slow. The use of sodium alginate to assist the formation of hydroxyapatite solves the problem that hydroxyapatite itself is brittle and difficult to form, and retains the characteristics of hydroxyapatite's high adsorption performance and porous structure. The hydroxyapatite pellets with a diameter of 1-5mm are obtained by the method of drop ball forming. This process is simple and controllable, and by controlling the size of the drip hole, small balls with different particle diameters are obtained; the prepared balls have high sphericity and particles The diameter is uniform and the strength is large. It can be used as a carrier for preparing catalysts or directly as a catalyst, adsorption material, and separation material. It is widely used in catalysis, adsorption separation, and bioengineering fields.

In order to have a more complete understanding of the embodiments of the present invention and its advantages, please refer to the following description and cooperate with the corresponding drawings. Must be emphasized Yes, various features are not drawn to scale and are for illustration purposes only. The content of the related diagrams is as follows:

[FIG. 1] is a photograph of spherical hydroxyapatite obtained in Example 1 of the present invention.

[FIG. 2] is a photograph of spherical hydroxyapatite obtained in Example 2 of the present invention.

[FIG. 3] is a photograph of spherical hydroxyapatite obtained in Example 3 of the present invention.

The manufacture and use of embodiments of the present invention are discussed in detail below. However, it can be understood that the embodiments provide many applicable inventive concepts that can be implemented in a variety of specific contents. The specific embodiments discussed are for illustration only and are not intended to limit the scope of the invention.

The technical solutions of the present invention are further described below through specific examples.

Example 1

Dissolve 74.8 g of anhydrous calcium chloride and 52.8 g of ammonium dihydrogen phosphate in 1600 mL of water, mix the calcium chloride solution and the ammonium dihydrogen phosphate solution under mechanical stirring, and adjust the pH of the solution to 10.4 with ammonia water. Stirring was continued for 15 min, placed in a 90°C water bath and stirred and heated for 2 hours, cooled at room temperature and left to age for 12 hours. The resulting precipitate was filtered with a Buchner funnel under reduced pressure. 6.69 g of the precipitate was dissolved in 15.61 g of deionized water to obtain 22.3 g of a hydroxyapatite dispersion liquid with a mass fraction of 30%. The dispersion liquid was added to 20 g of a sodium alginate solution with a mass percentage concentration of 3%, and dispersed with magnetic stirring for 30 min to obtain a suspension of hydroxyapatite. Take the above suspension droplets into a 300mL calcium nitrate aqueous solution with a volume molar concentration of 0.2M. After aging in the solution for 2 hours, it was taken out and dried at room temperature (25°C) for 48 hours, and calcined at 600°C for 2 hours to obtain spherical hydroxyapatite (as shown in Figure 1).

Example 2

The preparation procedure of the hydroxyapatite precipitate is the same as that in Example 1, and 8 g of the hydroxyapatite precipitate is added to 40 g of a sodium alginate solution with a mass percentage concentration of 1%, stirred and dispersed for 30 min to obtain a suspension of hydroxyapatite liquid. Take the above suspension droplets into a 300mL calcium nitrate solution with a volume molar concentration of 0.5M. After aging in the calcium nitrate solution for 10 hours, take out and dry at 60℃ for 24 hours, and roast at 500℃ for 3 hours , You can get spherical hydroxyapatite (as shown in Figure 2).

Example 3

The preparation procedure of the hydroxyapatite precipitate is the same as that in Example 1, and 6 g of the hydroxyapatite precipitate is added to 30 g of a sodium alginate solution with a mass percentage concentration of 2%, stirred and dispersed for 180 min to obtain a suspension of hydroxyapatite liquid. Take the above suspension droplets into a 300mL calcium nitrate solution with a volume molar concentration of 2M, after aging in the calcium nitrate solution for 1 hour, take out and dry at 120 ℃ for 8 hours, and calcined at 700 ℃ for 1 hour, The spherical hydroxyapatite can be obtained (as shown in Figure 3).

Example 4

The preparation procedure of the hydroxyapatite dispersion liquid is the same as that in Example 1, taking 22.3 g of the hydroxyapatite dispersion liquid with a mass fraction of 30%, adding 20 g of a sodium alginate solution with a mass percentage concentration of 3%, using a magnetic force Stir and disperse for 30 min to obtain a suspension of hydroxyapatite. Take the above suspended droplets into 200 mL and 0.1 M barium nitrate aqueous solution, after aging in barium nitrate solution for 15 hours, take out and dry at 80 ℃ for 12 hours, and roast at 600 ℃ for 2 hours, you can get barium doping Spherical hydroxyapatite.

Example 5

The preparation procedure of the hydroxyapatite precipitate is the same as that in Example 1, and 8 g of the hydroxyapatite precipitate is added to 40 g of a sodium alginate solution with a mass percentage concentration of 1%, stirred and dispersed for 30 min to obtain a suspension of hydroxyapatite liquid. Take the above suspension droplets into a 300mL copper sulfate solution with a molar molarity of 0.5M. After aging in the copper sulfate solution for 10 hours, take it out and dry it at 60°C for 36 hours, and roast at 350°C for 15 hours , You can get copper-doped spherical hydroxyapatite.

Claims (13)

A method for forming spherical hydroxyapatite, which is characterized by the following steps: (1) Stirring and mixing calcium chloride aqueous solution and ammonium dihydrogen phosphate aqueous solution, leaving to aging, filtering to obtain a precipitate, Disperse the precipitate directly into a deionized water to obtain a suspension containing hydroxyapatite; (2) The suspension containing the hydroxyapatite and an aqueous solution in which a soluble alginate is dissolved Mix thoroughly to make a mixed floating slurry; (3) Drop the mixed floating slurry into a solution containing a polyvalent metal cation salt to form a plurality of gel beads; (4) After aging, the gel beads are taken out, washed with deionized water, dried and roasted to prepare the spherical hydroxyapatite. The molding method as described in item 1 of the patent application range, characterized in that: the molar concentration of Ca ²⁺ of the calcium chloride aqueous solution in the step (1) is 0.1-0.5mol/L; the ammonium dihydrogen phosphate The molar concentration of PO ₄ ^3- in the aqueous solution is 0.05-0.3 mol/L; and the calcium chloride aqueous solution and the ammonium dihydrogen phosphate aqueous solution are mixed according to a molar ratio of Ca/P=1.67. The molding method as described in item 1 or 2 of the patent application range, characterized in that: during the stirring and mixing process of step (1), ammonia water needs to be added to control the pH value to 10-12; a stirring temperature is 80-100 ℃; one stirring time is 1-4 hours; one aging time is 10-24 hours. The molding method as described in item 1 of the patent application range, wherein the soluble alginate in step (2) is sodium alginate, potassium alginate, ammonium alginate, lithium alginate or magnesium alginate One or two or more. The molding method as described in item 1 of the patent application range, characterized in that the mass percentage concentration of the soluble alginate in the floating slurry in step (2) is 0.05% to 4%. The molding method as described in item 1 of the patent application range, characterized in that the mass percentage concentration of the hydroxyapatite in the floating slurry in the step (2) is 0.5% to 25%. The molding method as described in item 1 of the patent application range, characterized in that one of the multivalent metal cation salts in step (3) is calcium, strontium, barium, iron, cobalt, nickel, manganese , Copper, zinc or aluminum, one or two or more. The molding method as described in item 1 of the patent application range, characterized in that the concentration of the multivalent metal cation salt in the step (3) is 0.01 to 3 mol/L. The molding method as described in item 1 of the patent application range, wherein the aging time of the gel beads in step (4) is 0.1 to 24 hours. The molding method as described in item 1 of the patent application range, characterized in that: the drying temperature of the gel beads in step (4) is 20 to 150° C., and the time is 0.5 to 48 hours. The molding method as described in item 1 of the patent application range, characterized in that the calcination temperature of the gel beads in step (4) is 300 to 800° C., and the time is 0.2 to 48 hours. A hydroxyapatite pellet is produced by the molding method as described in any one of patent application items 1 to 11, characterized in that one of the hydroxyapatite pellets has a diameter of 1-5 mm. A hydroxyapatite pellet is produced by the molding method as described in any one of patent application items 1 to 11, wherein the hydroxyapatite pellet can be used in the field of catalysis, adsorption separation and bioengineering.

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