Volume 504, Issue 9 pp. 195-200
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Mechanism of Substitution in Carbonated Apatites

Prof. Dr. F. C. M. Driessens

Prof. Dr. F. C. M. Driessens

Inst. for Materials Science, Subfaculty of Dentistry, Catholic Univ., P.O. Box 9101, NL-6500 HB Nijmegen (The Netherlands)

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Dr. R. M. H. Verbeeck

Dr. R. M. H. Verbeeck

Research Associate of the N.F.S.R. (Belgium), Laboratory for Analyt. Chem., State Univ. Krijgslaan 281 - S12, B-9000 Ghent (Belgium)

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Lc. P. Kiekens

Lc. P. Kiekens

Research Associate of the N.F.S.R. (Belgium), Laboratory for Analyt. Chem., State Univ. Krijgslaan 281 - S12, B-9000 Ghent (Belgium)

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First published: September 1983
Citations: 36

Abstract

Single-phase AB-type carbonate apatites were prepared by sintering appropriate mixtures of CaHPO4 and CaCO3 at 870°C in a CO2 atmosphere with a partial water vapor pressure of 5 mm Hg. Chemical and physical analyses indicate that at a constant CO32−/OH ratio in the hydroxyl sublattice, carbonate substitutes for phosphate on a 1:1 mole basis. For every three PO43− ions substituted, two vacancies in the Ca2+ sublattice and one in the OH sublattice are created. The same substitution mechanism seems to apply in pure B-type carbonate apatite.

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