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Accommodation of the carbonate ion in apatite; an FTIR and X-ray structure study of crystals synthesized at 2-4 GPa

Michael E. Fleet, Xiaoyang Liu and Penelope L. King
Accommodation of the carbonate ion in apatite; an FTIR and X-ray structure study of crystals synthesized at 2-4 GPa
American Mineralogist (October 2004) 89 (10): 1422-1432

Abstract

Carbonated hydroxylapatite (C-OHAp) and carbonate apatite (CAp; x> or =0.5) in the composition series Ca (sub 10) (PO (sub 4) ) (sub 6-y) [(CO (sub 3) ) (sub x+(3/2)y) (OH) (sub 2-2x) ], x = 0.0-0.7, y = 0.0-0.6, have been synthesized at 2-4 GPa, and studied by FTIR spectroscopy and single-crystal X-ray diffraction. Three structural locations for the carbonate ion have been identified: (1) apatite channel, oriented with two oxygen atoms close to the c-axis (type A1); (2) close to a sloping face of the PO (sub 4) tetrahedron (type B); and, (3) stuffed channel position (type A2). Type A1 and B carbonate are equivalent to type A and B CAp of bone and enamel, whereas type A2 is a high-pressure feature. In type A CAp, ordering of type A1 carbonate within the apatite channel results in space group P3; all other apatites studied have average structures with P6 (sub 3) /m symmetry. Results for three new structures are: type A C-OHAp, x = 0.14, y = 0.0, a = 9.4468(4), c = 6.8806(4) Aa, and R (residual index of structure refinement) = 0.025; type B C-OHAp, x = 0.0, y = 0.17, a = 9.4234(2), c = 6.8801(3) Aa, and R = 0.025; and type A-B CAp, x = 0.7, y = 9.4817(6), c = 6.8843(3) Aa, and R = 0.025. A fourth structure analysis suggests that the type A-B CAp exchanges some of its channel carbonate with OH (super -) during room-temperature storage in nujol oil, with x and y reduced to 0.6 and 0.4, respectively. Local structural adjustments to accommodate the carbonate ion in the c-axis channel of OHAp include dilation of the channel, contraction of the Ca1O (sub n) polyhedron, and rotation of the PO (sub 4) tetrahedron about the P-O1 bond. The progressive increase in the a unit-cell edge length with increase in carbonate content of type A CAp is readily attributed to the dilation of the apatite channel. Carbonate-for-phosphate substitution in OHAp (type B CAp) requires displacement of O3 along + or -[001] and, thus, results in expansion of c (and contraction of a).


ISSN: 0003-004X
EISSN: 1945-3027
Coden: AMMIAY
Serial Title: American Mineralogist
Serial Volume: 89
Serial Issue: 10
Title: Accommodation of the carbonate ion in apatite; an FTIR and X-ray structure study of crystals synthesized at 2-4 GPa
Affiliation: University of Western Ontario, Department of Earth Sciences, London, ON, Canada
Pages: 1422-1432
Published: 200410
Text Language: English
Publisher: Mineralogical Society of America, Washington, DC, United States
References: 45
Accession Number: 2005-004577
Categories: Mineralogy of non-silicatesGeneral geophysics
Document Type: Serial
Bibliographic Level: Analytic
Illustration Description: illus. incl. 7 tables
Country of Publication: United States
Secondary Affiliation: GeoRef, Copyright 2018, American Geosciences Institute.
Update Code: 200502
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