A multi-domain gem-grade Brazilian apatite
dc.contributor.author | Baikie, T | en_AU |
dc.contributor.author | Schreyer, MK | en_AU |
dc.contributor.author | Wong, CL | en_AU |
dc.contributor.author | Pramana, SS | en_AU |
dc.contributor.author | Klooster, WT | en_AU |
dc.contributor.author | Ferraris, C | en_AU |
dc.contributor.author | McIntyre, GJ | en_AU |
dc.contributor.author | White, TJ | en_AU |
dc.date.accessioned | 2014-04-04T02:44:23Z | en_AU |
dc.date.available | 2014-04-04T02:44:23Z | en_AU |
dc.date.issued | 2012-10-01 | en_AU |
dc.date.statistics | 2014-04-04 | en_AU |
dc.description.abstract | 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. © 2012, Mineralogical Society of America. | en_AU |
dc.identifier.citation | Baikie, T., Schreyer, M. K., Wong, C. L., Pramana, S. S., Klooster, W. T., Ferraris, C., McIntyre, G. J., & White, T. J. (2012). A multi-domain gem-grade Brazilian apatite. American Mineralogist, 97(10), 1574-1581. doi:10.2138/am.2012.4069 | en_AU |
dc.identifier.govdoc | 4588 | en_AU |
dc.identifier.issn | 0003-004X | en_AU |
dc.identifier.issue | 10 | en_AU |
dc.identifier.journaltitle | American Mineralogist | en_AU |
dc.identifier.pagination | 1574-1581 | en_AU |
dc.identifier.uri | http://dx.doi.org/10.2138/am.2012.4069 | en_AU |
dc.identifier.uri | http://apo.ansto.gov.au/dspace/handle/10238/5402 | en_AU |
dc.identifier.volume | 97 | en_AU |
dc.language.iso | en | en_AU |
dc.publisher | De Gruyter | en_AU |
dc.subject | Brazil | en_AU |
dc.subject | Apatites | en_AU |
dc.subject | Synchrotrons | en_AU |
dc.subject | X-ray diffraction | en_AU |
dc.subject | Neutron diffraction | en_AU |
dc.subject | Calcium | en_AU |
dc.title | A multi-domain gem-grade Brazilian apatite | en_AU |
dc.type | Journal Article | en_AU |
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