A multi-domain gem-grade Brazilian apatite

A gem-grade apatite from Brazil of general composition (Ca,Na)10[(P,Si,S)O4]6(F,Cl,OH)2 has been studied using single-crystal X-ray and neutron diffraction together with synchrotron powder X-ray diffraction. Earlier electron microscopy studies had shown the nominally single-phase apatite contains an...

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Main Authors: Baikie, Tom, Schreyer, Martin K., Wong, Chui Ling, Pramana, Stevin S., Klooster, Wim T., Ferraris, Cristiano, McIntyre, Garry J., White, Timothy John
Other Authors: School of Materials Science & Engineering
Format: Journal Article
Language:English
Published: 2013
Subjects:
Online Access:https://hdl.handle.net/10356/98365
http://hdl.handle.net/10220/12451
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author Baikie, Tom
Schreyer, Martin K.
Wong, Chui Ling
Pramana, Stevin S.
Klooster, Wim T.
Ferraris, Cristiano
McIntyre, Garry J.
White, Timothy John
author2 School of Materials Science & Engineering
author_facet School of Materials Science & Engineering
Baikie, Tom
Schreyer, Martin K.
Wong, Chui Ling
Pramana, Stevin S.
Klooster, Wim T.
Ferraris, Cristiano
McIntyre, Garry J.
White, Timothy John
author_sort Baikie, Tom
collection NTU
description A gem-grade apatite from Brazil of general composition (Ca,Na)10[(P,Si,S)O4]6(F,Cl,OH)2 has been studied using single-crystal X-ray and neutron diffraction together with synchrotron powder X-ray diffraction. Earlier electron microscopy studies had shown the nominally single-phase apatite contains an abundant fluorapatite (F-Ap) host, together with chloro-hydroxylapatites (Cl/OH-Ap) guest phases that encapsulate hydroxylellestadite (OH-El) nanocrystals. While the latter features appear as small (200–400 nm) chemically distinct regions by transmission electron microscopy, and can be identified as separate phases by synchrotron powder X-ray diffraction, these could not be detected by single-crystal X-ray and neutron analysis. The observations using neutron, X-ray and electron probes are however consistent and complementary. After refinement in the space group P63/m the tunnel anions F− are fixed at z = ¼ along <001>, while the anions Cl− and OH− are disordered, with the suggestion that O-H···O-H··· hydrogen-bonded chains form in localized regions, such that no net poling results. The major cations are located in the 4f AFO6 metaprism (Ca+Na), 6h ATO6X tunnel site (Ca only), and 6h BO4 tetrahedron (P+Si+S). The structural intricacy of this gem stone provides further evidence that apatite microstructures display a nano-phase separation that is generally unrecognized, with the implication that such complexity may impact upon the functionality of technological analogues.
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spelling ntu-10356/983652023-07-14T15:54:40Z A multi-domain gem-grade Brazilian apatite Baikie, Tom Schreyer, Martin K. Wong, Chui Ling Pramana, Stevin S. Klooster, Wim T. Ferraris, Cristiano McIntyre, Garry J. White, Timothy John School of Materials Science & Engineering Apatite X-ray diffraction Laue neutron diffraction Synchrotron X-ray diffraction A gem-grade apatite from Brazil of general composition (Ca,Na)10[(P,Si,S)O4]6(F,Cl,OH)2 has been studied using single-crystal X-ray and neutron diffraction together with synchrotron powder X-ray diffraction. Earlier electron microscopy studies had shown the nominally single-phase apatite contains an abundant fluorapatite (F-Ap) host, together with chloro-hydroxylapatites (Cl/OH-Ap) guest phases that encapsulate hydroxylellestadite (OH-El) nanocrystals. While the latter features appear as small (200–400 nm) chemically distinct regions by transmission electron microscopy, and can be identified as separate phases by synchrotron powder X-ray diffraction, these could not be detected by single-crystal X-ray and neutron analysis. The observations using neutron, X-ray and electron probes are however consistent and complementary. After refinement in the space group P63/m the tunnel anions F− are fixed at z = ¼ along <001>, while the anions Cl− and OH− are disordered, with the suggestion that O-H···O-H··· hydrogen-bonded chains form in localized regions, such that no net poling results. The major cations are located in the 4f AFO6 metaprism (Ca+Na), 6h ATO6X tunnel site (Ca only), and 6h BO4 tetrahedron (P+Si+S). The structural intricacy of this gem stone provides further evidence that apatite microstructures display a nano-phase separation that is generally unrecognized, with the implication that such complexity may impact upon the functionality of technological analogues. Accepted version 2013-07-29T06:13:45Z 2019-12-06T19:54:13Z 2013-07-29T06:13:45Z 2019-12-06T19:54:13Z 2012 2012 Journal Article Baikie, T., Schreyer, M. K., Wong, C. L., Pramana, S. S., Klooster, W. T., Ferraris, C., et al. (2012). A multi-domain gem-grade Brazilian apatite. American Mineralogist, 97(10), 1574-1581. 0003-004X https://hdl.handle.net/10356/98365 http://hdl.handle.net/10220/12451 10.2138/am.2012.4069 en American mineralogist © 2012 Mineralogical Society of America. This is the author created version of a work that has been peer reviewed and accepted for publication by American mineralogist, Mineralogical Society of America. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.2138/am.2012.4069]. application/pdf
spellingShingle Apatite
X-ray diffraction
Laue neutron diffraction
Synchrotron X-ray diffraction
Baikie, Tom
Schreyer, Martin K.
Wong, Chui Ling
Pramana, Stevin S.
Klooster, Wim T.
Ferraris, Cristiano
McIntyre, Garry J.
White, Timothy John
A multi-domain gem-grade Brazilian apatite
title A multi-domain gem-grade Brazilian apatite
title_full A multi-domain gem-grade Brazilian apatite
title_fullStr A multi-domain gem-grade Brazilian apatite
title_full_unstemmed A multi-domain gem-grade Brazilian apatite
title_short A multi-domain gem-grade Brazilian apatite
title_sort multi domain gem grade brazilian apatite
topic Apatite
X-ray diffraction
Laue neutron diffraction
Synchrotron X-ray diffraction
url https://hdl.handle.net/10356/98365
http://hdl.handle.net/10220/12451
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