CA1155633A - Process for producing hydroxyapatite - Google Patents

Process for producing hydroxyapatite

Info

Publication number
CA1155633A
CA1155633A CA000390324A CA390324A CA1155633A CA 1155633 A CA1155633 A CA 1155633A CA 000390324 A CA000390324 A CA 000390324A CA 390324 A CA390324 A CA 390324A CA 1155633 A CA1155633 A CA 1155633A
Authority
CA
Canada
Prior art keywords
stage
reaction
slurry
tcp
conducted
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CA000390324A
Other languages
French (fr)
Inventor
James F. Conn
Leofwin A. Jessen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Astaris LLC
Monsanto Co
Original Assignee
Monsanto Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Monsanto Co filed Critical Monsanto Co
Application granted granted Critical
Publication of CA1155633A publication Critical patent/CA1155633A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B25/00Phosphorus; Compounds thereof
    • C01B25/16Oxyacids of phosphorus; Salts thereof
    • C01B25/26Phosphates
    • C01B25/32Phosphates of magnesium, calcium, strontium, or barium
    • C01B25/322Preparation by neutralisation of orthophosphoric acid

Abstract

PROCESS FOR PRODUCING HYDROXYAPATITE
Abstract of the Invention A continuous process for producing hydroxy-apatite which comprises a two-stage reaction in which pH control and reactant flow are carefully regulated.

Description

PROCESS FOR PRODUCING HYDROXYAPATITE
Background of the Invention . This invention relates to the production of hydroxyapatite, hereinafter referred to as tricalcium phosphate or "TCP".
The batch preparation of TCP by the reaction of lime and phosphoric acid is well known. Due to the inherent nature of batch reaction, however, the volume of TC~ produced thereby is necessarily less than could be produced by a continuous process. For example, U.S. 3,387,925 discloses a batch reaction of lime and phosphoric acid wherein the particle size of the TCP is controlled in order to obtain a precipitate of fine particles~ In accordance with the invention : 15 of the aforementioned patent, it was found that a smaller particle size may be produced by controlling the final pH, the reaction temperature and the rate of addition of the reactants. Thus, the temperature of the reaction is kept within a range of from about 20 to 50C., the lime slurry is continuously agitated to prevent localized acid build-up and the 20~ aqueous phosphoric acid which is used is added to the lime slurry as quickly as possible until the lime slurry is neutralized to a pH of between about 6.7 and 8.5.
Summary of the Invention In accordance with the present invention, there is disclosed a process for producing TCP in - 11556~3 large volumes which comprises continuously charging to the first stage of a two-stage reactor a slurry of calcium oxide in water and a solution of phos-phoric acid in water. The lime slurry and the solu-tion of phosphoric acid in water are then allowed to react in the first stage under vigorous agitation at a pH such that the viscosity of the reaction mass is near minimum viscosity, i.e. a pH of from about 9.5 to about ll. The reaction is then continued in the second stage of the reactor under vigorous agitation while continuously charging additional solution of aqueous phosphoric acid in an amount sufficient to maintain the pH in the second stage at about 7.0 to about 7.4. The TCP reactant product is continuously removed from the reactor.
Specific Embodiments of the Invention The primary reaction of the present invention is as follows:
( H)2 6 H3PO4 > 3[Ca3(Po4)2]-ca(oH)2 + 18 E2O
This reaction gives a 100% yield of product.
The reaction is conducted in a two-stage reactor wherein the rate of flow of phosphoric acid and lime slurry is adjusted so that from about 70 to about 94% of the lime slurry is converted in the first stage and the remaining portion is converted in the second stage. It is preferred that approximately 90%
of the reaction be completed in the first stage for best quality product. Above about 94% completion of reaction in the first stage affords a product which is unsatis-factory because of high bulk density.
When phosphoric acid is added to lime slurry at a pH above about 7, hydroxyapatite precipitates as a solid phase. In order to precipitate hydroxyapatite with low bulk density and high surface area, the pre-cipitation must be carried out at a pH above about lO.

- 1 155~

Accordingly, a two-stage reactor is required to pro-duce hydroxyapatite on a continuous basis. Both stages must have vigorous agitation. The phosphoric acid is added in the first stage in a manner suitable to disperse the acid so that high local concentrations of acid are avoided.
The major process variables are (l) the lime/
acid ratio, (2) pH and (3) agitation. The rates of acid flow and lime flow must be adjusted such that about 90% of the lime is converted to hydroxyapatite in the first stage and the remaining 10% is converted in the second stage. The ratio is controlled indirect-ly by avoiding high local acid concentration or high local lime concentration.
Control of pH is vital to the successful control of the process. It is important to hold the pH in stage one between about 9.5 to about 11. A pH
o~ 9.5-10 indicates that the reaction in stage one is approaching 100% and the viscosity of the reaction mass approaches a maximum where agitation becomes less efficient. A pH above about 11 indicates that the extent of reaction is too low in stage one. Deviation from a pH of from about 9.5 to about 11, preferably from about lO to about 11 and, more preferably, at about 10.5 indicates that either acid or lime flow is not correct and must be adjusted. Phosphoric acid delivery to the second stage is controlled in such a manner as to hold the pH at about 7.0 to about 7.4, preferably from about 7.2 to about 7.3. It is impor-tant to have accurate pH control at this point to pro-duce quality product.
The most critical variable in the process is agitation. Agitation in both stages is very difficult because of the high viscosity of the slurry. Excellent agitation is required in the first stage to form a 1 155~3 quality product. Poor agitation in the first stage affords an overflow product to the second stage containing entrapped, unreacted lime which cannot be reacted in the second stage. This causes the pH of the dried final product to go up to pH 8-9 when re-slurried in water. Alternately, high local concen-trations of phosphoric acid must be avoided to prevent the formation of dicalcium phosphate which is impossi-ble to convert to the desired hydroxyapatite. Effi-cient agitation is very important in the second stage to obtain equilibrium so that the pH of the final product slurry will not drift. The viscosity in the second stage is higher than it is in the first stage and thus more efficient agitation is necessary. In-sufficient agitation will result in a rapid, wide change in pH as unmixed portions of different pH are carried through the process.
The temperature at which the reaction is carried out has little effect on the product quality or on the efficiency of the process. Accordingly, temperatures from 35 to 90C. are satisfactory.
EXAMPLE
To a two-stage reactor having a 26.5 1. stain-less steel first stage and a glass lined 79.5 1. second - 25 stage equipped with acid and lime feed lines, an overflow trough from the first stage to the second stage, product outlet in the second stage and high efficiency agitators, was added lime slurry (30~ sus-pension in water) and 80% phosphoric acid at a rate such that 31.3 kg. of lime and 70.8 kg. of acid were added per hour. The flow rate provided an acid/lime ratio such that 90% reaction at a temperature of about 70-85C. occurred in the first stage. A pH of about 10.5 was held in the first stage by means of flow controllers coupled to pH probes. After 15 min., the 1 1556~3 suspension overflowed to the second stage where phos-phoric acid (80~) was automatically fed by means of flow controllers coupled to pH probes which were cali-brated to maintaln a pH of about 7.2-7.4. After 45 min. in the second stage, a 30~ suspension of TCP in water overflowed to a flash dryer. The suspension was flash-dried to produce 45.4 kg./hr. of submicron, powdered TCP.

Claims (10)

The embodiments of the invention in which an exclu-sive property or privilege is claimed are defined as follows:
1. A process for producing TCP comprising continuously charging to the first stage of a two-stage reactor a slurry of calcium oxide in water and a solution of phosphoric acid in water, allowing such slurry and such solution to react in said first stage under vigorous agitation at a pH such that the vis-cosity of the reaction mass is near minimum viscosity, continuing said reaction in the second stage of said reactor under vigorous agitation while continuously charging additional solution of phosphoric acid thereto in an amount sufficient to maintain the pH in said second stage at about 7.0 to about 7.4 and continuously removing a suspension of TCP from said second stage.
2. Process of Claim 1 wherein said first stage reaction is conducted at a pH of from about 9.5 to about 11.
3. Process of Claim 2 wherein said first stage reaction is conducted at a pH of about 10.5.
4. Process of Claim 1 wherein said second stage reaction is conducted at a pH of from about 7.2 to about 7.3.
5. Process of Claim 2 wherein said second stage reaction is conducted at a pH of from about 7.2 to about 7.3.
6. Process of Claim 3 wherein said second stage reaction is conducted at a pH of from about 7.2 to about 7.3.
7. Process of Claim 1 wherein the rate of charging of said phosphoric acid solution and said lime slurry is maintained at a ratio such that from about 70 to about 94 percent of said slurry is converted to TCP
in said first stage and from about 6 to about 30 percent of said slurry is converted in said second stage.
8. Process of Claim 7 wherein said ratio is maintained such that about 90 percent of said slurry is converted to TCP in said first stage and about 10 percent of said slurry is converted in said second stage.
9. Process of Claim 1 wherein said reaction is carried out at a temperature of from about 35° to about 90°C.
10. Process of Claim 1 wherein said suspen-sion of TCP is flash-dried to afford submicron, powdered TCP.
CA000390324A 1980-11-19 1981-11-18 Process for producing hydroxyapatite Expired CA1155633A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US208,224 1980-11-19
US06/208,224 US4324772A (en) 1980-11-19 1980-11-19 Process for producing hydroxyapatite

Publications (1)

Publication Number Publication Date
CA1155633A true CA1155633A (en) 1983-10-25

Family

ID=22773751

Family Applications (1)

Application Number Title Priority Date Filing Date
CA000390324A Expired CA1155633A (en) 1980-11-19 1981-11-18 Process for producing hydroxyapatite

Country Status (5)

Country Link
US (1) US4324772A (en)
EP (1) EP0052508A1 (en)
JP (1) JPS57111217A (en)
BR (1) BR8107506A (en)
CA (1) CA1155633A (en)

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JPS5654841A (en) * 1979-10-08 1981-05-15 Mitsubishi Mining & Cement Co Bone broken portion and filler for void portion and method of treating bone of animal using said filler
US4673355A (en) * 1982-10-25 1987-06-16 Farris Edward T Solid calcium phosphate materials
US4481175A (en) * 1982-12-14 1984-11-06 Mitsui Toatsu Chemicals, Inc. Process for preparing apatite
US4880610A (en) * 1988-04-20 1989-11-14 Norian Corporation In situ calcium phosphate minerals--method and composition
US5962028A (en) * 1988-04-20 1999-10-05 Norian Corporation Carbonated hydroxyapatite compositions and uses
US4849193A (en) * 1988-05-02 1989-07-18 United States Gypsum Company Process of preparing hydroxylapatite
DE4037103C1 (en) * 1990-11-22 1992-01-09 Bk Ladenburg Gmbh Gesellschaft Fuer Chemische Erzeugnisse, 6802 Ladenburg, De
DE4232443C1 (en) * 1992-09-28 1993-09-23 Bk Ladenburg Gmbh Gesellschaft Fuer Chemische Erzeugnisse, 68526 Ladenburg, De
CA2142663A1 (en) * 1994-02-28 1995-08-29 Jean Marie Bacardi Process for preparing calcium salts of low aluminum content
US5639402A (en) * 1994-08-08 1997-06-17 Barlow; Joel W. Method for fabricating artificial bone implant green parts
US5948458A (en) * 1996-12-19 1999-09-07 Rhodia Inc. Method for preventing spoilage, rancidity, and off-color by using a tricalcium phosphate ultraviolet light inhibitor
US6013591A (en) 1997-01-16 2000-01-11 Massachusetts Institute Of Technology Nanocrystalline apatites and composites, prostheses incorporating them, and method for their production
EP0901773A1 (en) 1997-08-15 1999-03-17 David E. Gibbs Resorbable implant
US6010977A (en) * 1998-06-24 2000-01-04 Eastman Chemical Company Preparation of sub-visual molecular aggregrates composed of antimony phosphate derivatives
FR2799193B1 (en) * 1999-10-04 2002-03-15 Toulouse Inst Nat Polytech PROCESS FOR OBTAINING APATITE POWDER OF DEFINED CHEMICAL COMPOSITION AND CONTROLLED GRANULOMETRY
AU2000267174A1 (en) * 2000-07-03 2002-01-14 Zakrytoe Aktsionernoe Obschestvo "Ostim" Method for producing nano-sized crystalline hydroxyapatite
KR100511338B1 (en) * 2002-02-26 2005-08-31 재단법인서울대학교산학협력재단 Calcium phosphate colloids, dots, islands, thin films or granules and its preparation
TW200400062A (en) 2002-04-03 2004-01-01 Mathys Medizinaltechnik Ag Kneadable, pliable bone replacement material
US20050036959A1 (en) * 2003-08-15 2005-02-17 Sayed Ibrahim Rapid temporary tooth whitening composition
US20050069501A1 (en) * 2003-08-15 2005-03-31 Sayed Ibrahim Rapid temporary tooth whitening composition
US20100040668A1 (en) * 2006-01-12 2010-02-18 Rutgers, The State University Of New Jersey Biomimetic Hydroxyapatite Composite Materials and Methods for the Preparation Thereof
US8287914B2 (en) 2006-01-12 2012-10-16 Rutgers, The State University Of New Jersey Biomimetic hydroxyapatite synthesis
US20080221681A1 (en) * 2007-03-09 2008-09-11 Warsaw Orthopedic, Inc. Methods for Improving Fatigue Performance of Implants With Osteointegrating Coatings
US20080221688A1 (en) * 2007-03-09 2008-09-11 Warsaw Orthopedic, Inc. Method of Maintaining Fatigue Performance In A Bone-Engaging Implant
RU2505479C1 (en) * 2012-06-28 2014-01-27 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Российский химико-технологический университет им. Д.И. Менделеева" (РХТУ им. Д.И. Менделеева) Method of obtaining hydroxyapatite
BR112018005871A2 (en) * 2015-09-25 2018-10-16 Clean World Tech Ltd production of calcium phosphate compositions

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3387925A (en) * 1966-03-16 1968-06-11 Stauffer Chemical Co Polymer suspension stabilizer
US3409394A (en) * 1967-12-22 1968-11-05 James P. Sprigg Method of producing phosphate granules by reacting phosphoric acid and a carbonate with controlled reaction times
US4139599A (en) * 1973-01-11 1979-02-13 Colgate Palmolive Company Process for preparing dicalcium phosphate dihydrate having a portion of the calcium displaced by divalent metal ion
GB1586915A (en) * 1978-03-10 1981-03-25 British Charcoals & Macdonalds Synthetic bone ash

Also Published As

Publication number Publication date
BR8107506A (en) 1982-08-10
JPS57111217A (en) 1982-07-10
EP0052508A1 (en) 1982-05-26
US4324772A (en) 1982-04-13
JPH0214283B2 (en) 1990-04-06

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