CN1631773A

CN1631773A - Preparation method of hydroxyapatite

Info

Publication number: CN1631773A
Application number: CN 200410067736
Authority: CN
Inventors: 侯小宝; 谢田甜; 刘志信; 夏志军
Original assignee: Ningbo Economic & Technology Development Zone Jingge New Material Development Co
Current assignee: Ningbo Economic & Technology Development Zone Jingge New Material Development Co
Priority date: 2004-10-29
Filing date: 2004-10-29
Publication date: 2005-06-29
Anticipated expiration: 2024-10-29
Also published as: CN1268540C

Abstract

The invention is preparation of hydroxyl group apatite at middle and low temperature direct by conch one step process. The invention uses the conch powder as rough material mixed with hydrogen sulfate solution and pyrolyzes 6 to 48 hours at temperature of 90 to 105 deg C. After the reaction collate and dry to obtain the hydroxyl group apatite powder. The rough material shell in the invention has a broad source and low price. The preparation is very simple which is just one step to convert shell directly to hydroxyl group apatite so to greatly lower the prepare cost of the hydroxyl group apatite.

Description

Preparation method of hydroxyapatite

Technical Field

The invention relates to a method for synthesizing hydroxyapatite, in particular to a method for directly synthesizing hydroxyapatite from shells by a one-step low-temperature hydrothermal method, belonging to the field of inorganic synthesis.

Background

Hydroxyapatite (HAP) is prepared by a number of methods, which can be roughly classified into three types: dry (solid phase reaction), hydrothermal, and wet (solution reaction).

1) Dry process (solid phase reaction process)

The current general method is Ca₃(PO₄)₂Or CaCO₃And Ca₄P₂O₉HAP was synthesized by solid-phase reaction by introducing steam at a high temperature of 1200 ℃. The temperature of the reaction must be controlled because sintering is carried out at 1200 deg.CAt the temperature, the crystal phase of the reaction product is HAP; and at the sintering temperature of 1250 ℃, the crystal phase is a mixture of HAP and TCP. During the reaction, steam must be introduced at a high temperature to suppress decomposition of HAP. The method has the advantage that HAP crystals free of lattice defects and having a high degree of crystallinity can be obtained. The disadvantages are that the raw material powder needs to be mixed and ground for a long time, the pollution is easy, the reaction speed is slow, the particle size of the product is large, and the activity of the product is poor.

2) Hydrothermal method

The hydrothermal synthesis method is to dissolve and recrystallize substances which are difficult to dissolve or insoluble under normal conditions by heating a reaction vessel in a closed pressure vessel with an aqueous solution as a reaction medium.Mixing Ca (NO)₃)₂And H₃PO₄Mixing uniformly according to the calcium-phosphorus ratio Ca/P of 1.67, putting into a special closed pressure cooker, and adding distilled water. Heating to different temperatures (200-400 ℃) at a heating speed of 7 ℃/min, and carrying out hydrothermal reaction at a specified temperature to enable [ OH [ -O]]]Adding into crystal lattice to generate HAP. The reaction equation is as follows:

；

taking out HAP crystal when the reaction vessel is cooled to room temperature, repeatedly cleaning with deionized water, and adding Ca (OH)₂And (5) drying.

The method has the greatest advantage that the product is directly crystalline, sintering crystallization is not needed, and agglomeration which is difficult to avoid in the sintering process can be reduced. The granularity is uniform, and the form is relatively regular; moreover, the reaction conditions are changed to obtain products with different crystal structures and crystal forms. With the increase of the hydrothermal synthesis temperature and the prolonging of the time, the more complete the crystal grain development and the larger the grain size. However, this method requires a high level of equipment and is also costly.

3) Wet process

The wet reaction comprises an acid-base reaction method, a hydrolysis method, an electrochemical deposition method, a sol-gel method, a microemulsion method and the like.

The acid-base reaction method is based on the neutralization reaction of acid and base to generate HAP. Such as with Ca (OH)₂And H₃PO₄The reaction produces HAP. Firstly, a certain amount of Ca (OH)₂Powder of (2)Mixing with water to obtain paste, adding Ca (OH) into a beaker containing distilled water and heated to about 70 deg.C₂Stirring, slowly adding H dropwise₃PO₄And adjusting the pH value to generate HAP. The method is simple and convenient to operate, is most economical and does not need to be complicatedThe equipment is more suitable for industrial production.

The hydrolysis method and the hydrothermal synthesis method have similar principles. In the hydrolysis process, CaHPO is generally used₄At about 70 ℃ and pH 8.5 [ OH]]Adding into crystal lattice to generate HAP.

The basic principle of the sol-gel method is to hydrolyze a metal alkoxide or an inorganic salt, and then to polymerize the solute into a gel, dry and bake. The technical method is that Ca sol is slowly dropped into PO₄ ⁽²⁺⁾In the sol, different amounts of NH are respectively added into the system₄HCO₃Adjusting the pH value with ammonia water, and aging the generated CHAP gel for 24h → washing → drying → roasting to obtain the HAP. The method has simple process, easily controlled product composition and no need of large-scale equipment, and is widely applied to preparing various high-purity and uniform superfine powders.

The material system Lim of Singapore national university adopts micro-emulsion method to prepare nano HAP, and the technical method is that CaCl is added₂And (NH)₄)₂HPO₄Preparing microemulsion respectively, wherein the oil phase is cyclohexanol and the surfactant is n-hexane, mixing the two microemulsions, standing for a certain time, and washing the precipitate with absolute ethyl alcohol to obtain HAP powder with the particle size of 20-40 nm.

In addition, there are electrochemical deposition methods. From Ca, according to the basic principle of electrochemistry₃(PO₄)₂The HAP particles are electrodeposited in an aqueous solution on a cathode.

Disclosure of Invention

The invention aims to provide a method for directly synthesizing hydroxyapatite from shells at low temperature by a one-step method, thereby simplifying the processing technology and greatly reducing the preparation cost of the hydroxyapatite.

The technical problem of the invention is mainly solved by the following technical scheme: the preparation method of the hydroxyapatite adopts shell powder as a raw material, and comprises the steps of mixing a shell with an aqueous solution of hydrogen phosphate, heating and reacting for 6-48 hours in a closed container at 90-105 ℃, filtering and drying after the reaction is finished to obtain the hydroxyapatite powder.

In order to improve the quality of finished products and accelerate the reaction speed, the particle size of the powder is preferably less than 1 mm, the aqueous solution of the hydrogen phosphate is deionized water, the deionized water is stirred during the reaction, and the powder is washed before the reaction is finished and filtered.

The dosage ratio of the shell powder and the water is approximately between 16g to 800 ml.

Therefore, compared with the traditional preparation method of hydroxyapatite, the method has the following characteristics and advantages:

1. the raw material adopted by the invention is the shell, belongs to waste resources, has wide sources and low price, and greatly reduces the preparation cost of the hydroxyapatite;

2. the preparation method is very simple, and the shell powder can be directly converted into the hydroxyapatite by a one-step method.

Detailed Description

The technical solution of the present invention will be further specifically described below by way of examples.

The first embodiment is as follows:

weighing 16g of freshwater mussel shell powder, 22 g of chemically pure ammonium dihydrogen phosphate, mixing with 800ml of deionized water, pouring into a 1L flask, stirring in a water bath at 90 ℃ for reaction for 48 hours, filtering, washing, and drying in a 90 ℃ oven to obtain hydroxyapatite with the purity of 94.6% and the size of 50-150 microns.

Example two:

weighing 20 g of Donghai mussel powder, 25 g of industrial sodium dihydrogen phosphate, mixing with 1000 ml of deionized water, pouring into a 1L flask, stirring in a water bath at 97-98 ℃ for reaction for 27 hours, filtering, washing, and drying in a 90 ℃ oven to obtain hydroxyapatite with purity of 88.3% and size of 40-100 microns.

Example three:

weighing 16g of clam shell powder, 12.68 g of chemically pure ammonium dihydrogen phosphate and 15.0 g of chemically pure diammonium hydrogen phosphate, mixing with 800ml of deionized water, pouring into a 1L flask, stirring in a water bath at 105 ℃ for reaction for 6 hours, filtering, washing, and drying in an oven at 90 ℃ to obtain hydroxyapatite with the purity of 97.8 percent and the size of 20-40 nanometers.

Example four:

weighing 16g of Donghai mussel shell powder, 14 g of chemically pure potassium dihydrogen phosphate and 15 g of chemically pure dipotassium hydrogen phosphate, mixing with 800ml of deionized water, pouring into a 1L flask, stirring in a water bath at 95 ℃ for reacting for 18 hours, filtering, washing, and drying in an oven at 90 ℃ to obtain hydroxyapatite powder with the purity of 96.6% and the size of 2-50 microns.

Claims

1. A preparation method of hydroxyapatite is characterized in that: the method comprises the steps of mixing shell powder serving as a raw material with an aqueous solution of hydrogen phosphate, heating and reacting in a closed container at 90-105 ℃ for 6-48 hours, filtering after the reaction is finished, and drying to obtain hydroxyapatite powder.

2. The method for preparing hydroxyapatite according to claim 1, characterized in that: the particle size of the powder is less than 1 mm; the aqueous solution of the hydrogen phosphate adopts deionized water; stirring during the reaction; after the reaction, the mixture was filtered and washed.