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Method of producing fluoroapatite, fluoroapatite, and adsortion apparatus

a technology of adsorption apparatus and fluoroapatite, which is applied in the direction of phosphorus halides/oxyhalides, chemistry apparatus and processes, and other chemical processes, can solve the problems of difficult to remove ammonia from particles, difficult to obtain particles having uniform characteristics, and ammonia remains, so as to improve the acid resistance of the produced fluoroapatite and crystallize high. the effect of high crystallinity

Inactive Publication Date: 2010-05-27
HOYA CORP
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0009]It is objects of the present invention to provide a method of producing fluoroapatite having improved acid resistance by reducing an impurity, such as ammonia, derived from a raw material to a low or very low level, fluoroapatite having high acid resistance, and an adsorption apparatus using such fluoroapatite.

Problems solved by technology

However, the fluoroapatite synthesized by such a method contains ammonia adsorbed thereto as an impurity.
Apatites such as fluoroapatite have a high ability to adsorb ammonia, and therefore in a case where a slurry containing synthesized fluoroapatite is spray-dried (granulated) to obtain particles, ammonia remains in the particles (fluoroapatite particles) because it is very difficult to remove ammonia from the particles.
Therefore, an amount of ammonia remaining in the thus produced particles is different from lot to lot, which makes it difficult to obtain particles having uniform characteristics.
Further, ammonia remaining in fluoroapatite (particles) inhibits substitution of hydroxyl groups by fluorine atoms, and therefore there are also problems that a rate of the substitution of hydroxyl groups by fluorine atoms can be increased only to a certain extent and therefore it cannot be expected that acid resistance of fluoroapatite is further improved.

Method used

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  • Method of producing fluoroapatite, fluoroapatite, and adsortion apparatus
  • Method of producing fluoroapatite, fluoroapatite, and adsortion apparatus
  • Method of producing fluoroapatite, fluoroapatite, and adsortion apparatus

Examples

Experimental program
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Effect test

example 1

[0099]First, calcium hydroxide was suspended in pure water to obtain a calcium hydroxide suspension, and then an aqueous phosphoric acid solution was dropped into the calcium hydroxide suspension while the calcium hydroxide suspension was sufficiently stirred. As a result, 500 L of a slurry containing 10 wt % of hydroxyapatite primary particles was obtained.

[0100]It is to be noted that the thus obtained hydroxyapatite primary particles were found to be hydroxyapatite by powder X-ray diffractometry.

[0101]On the other hand, hydrogen fluoride was dissolved in pure water so that an amount thereof is 5 wt % to prepare a hydrogen fluoride-containing solution.

[0102]Then, 41.84 L of the hydrogen fluoride-containing solution was dropped into the slurry at a rate of 5 L / hr while the slurry was stirred at a stirring power of 1 kW.

[0103]It is to be noted that the slurry had a pH of 3.00 at the time when the dropping of the hydrogen fluoride-containing solution was completed. An amount of the hy...

example 2

[0110]Fluoroapatite primary particles, fluoroapatite dried particles, and fluoroapatite sintered particles 1 and 2 were produced in the same manner as in the Example 1 except that the pH of the slurry at the time of completion of the dropping of the hydrogen fluoride-containing solution was adjusted to 3.36 by adding pure water to the hydrogen fluoride-containing solution.

[0111]It is to be noted that the fluoroapatite primary particles had a rate of substitution of hydroxyl groups by fluorine atoms of about 75%. Further, as a result of powder X-ray diffraction of the fluoroapatite dried particles, any products other than the fluoroapatite were not detected.

[0112]It is also to be noted that the fluoroapatite dried particles had an average particle size of about 40 μm, and each of the two kinds of the fluoroapatite sintered particles 1 and 2 (adsorbents) also had an average particle size of about 40 μm.

example 3

[0113]Fluoroapatite primary particles, fluoroapatite dried particles, and fluoroapatite sintered particles 1 and 2 were produced in the same manner as in the Example 1 except that the pH of the slurry at the time of completion of the dropping of the hydrogen fluoride-containing solution was adjusted to 3.96 by adding pure water to the hydrogen fluoride-containing solution.

[0114]It is to be noted that the fluoroapatite primary particles had a rate of substitution of hydroxyl groups by fluorine atoms of about 50%. Further, as a result of powder x-ray diffraction of the fluoroapatite dried particles, any products other than the fluoroapatite and the hydroxyapatite were not detected.

[0115]It is also to be noted that the fluoroapatite dried particles had an average particle size of about 40 μm, and each of the two kinds of the fluoroapatite sintered particles 1 and 2 (adsorbents) also had an average particle size of about 40 μm.

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Abstract

A method of producing a fluoroapatite is provided. The method comprises preparing a slurry containing a hydroxyapatite which has at least one hydroxyl group, preparing a hydrogen fluoride-containing solution containing a hydrogen fluoride, mixing the hydrogen fluoride-containing solution with the slurry to obtain a mixture to thereby adjust a pH of the mixture in the range of 2.5 to 5, and reacting the hydroxyapatite with the hydrogen fluoride in the mixture in a state that the pH of the mixture is adjusted within the above range to thereby obtain the fluoroapatite by substituting the at least one hydroxyl group of the hydroxyapatite with fluorine atom of the hydrogen fluoride. The method can produce the fluoroapatite having improved acid resistance by reducing an impurity, such as ammonia, derived from a raw material to a low or very low level. Further, a fluoroapatite having high acid resistance is also provided. Furthermore, an adsorption apparatus using such a fluoroapatite is provided.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application is a divisional of U.S. patent application Ser. No. 12 / 184,459, filed Aug. 1, 2008, which claims priority to Japanese Application No. 2007-203553, filed Aug. 3, 2007, the contents of which are expressly incorporated by reference herein in their entirety.FIELD OF THE INVENTION[0002]The present invention relates to a method of producing fluoroapatite, fluoroapatite, and an adsorption apparatus, and in particular relates to a method of producing fluoroapatite, fluoroapatite that can be obtained by the method, and an adsorption apparatus that uses the fluoroapatite.BACKGROUND ART[0003]Fluoroapatite has almost the same crystalline structure as hydroxyapatite, and therefore shows almost the same adsorption characteristics (adsorption ability) to a protein as hydroxyapatite.[0004]Further, fluoroapatite is a substance that is stabler than hydroxyapatite, and therefore has high acid resistance. For these reasons, fluoroapatite has...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C01B25/10B01J20/04
CPCB01J20/048C01B25/455B01J20/3078B01J20/3028B01J20/281B01J20/04C01B25/32
Inventor ISHIKAWA, TSUYOSHIOGAWARA, YOSHIYUKIYOSHITAKE, TOMOHIKOMURAKAMI, YUKIKO
Owner HOYA CORP
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