Winter 2003 Gems & Gemology

Total Page:16

File Type:pdf, Size:1020Kb

Winter 2003 Gems & Gemology Winter 2003 VOLUME 39, NO. 4 EDITORIAL _____________ 267 Tomorrow’s Challenge: CVD Synthetic Diamonds William E. Boyajian FEATURE ARTICLES _____________ 268 Gem-Quality Synthetic Diamonds Grown by a Chemical Vapor Deposition (CVD) Method Wuyi Wang, Thomas Moses, Robert C. Linares, James E. Shigley, Matthew Hall, and James E. Butler pg. 269 Description and identifying characteristics of Apollo Diamond Inc.’s facetable, single-crystal type IIa CVD-grown synthetic diamonds. 284 Pezzottaite from Ambatovita, Madagascar: A New Gem Mineral Brendan M. Laurs, William B. (Skip) Simmons, George R. Rossman, Elizabeth P. Quinn, Shane F. McClure, Adolf Peretti, Thomas Armbruster, Frank C. Hawthorne, Alexander U. Falster, Detlef Günther, Mark A. Cooper, and Bernard Grobéty A look at the history, geology, composition, and properties of this new cesium-rich member of the beryl group. 302 Red Beryl from Utah: A Review and Update James E. Shigley, Timothy J. Thompson, and Jeffrey D. Keith A report on the geology, history, and current status of the world’s only known occurrence of gem-quality red beryl. pg. 299 REGULAR FEATURES _____________________ 314 Lab Notes • Chrysocolla “owl” agate • Red coral • Coated diamonds • Natural emerald with nail-head spicules • Emerald with strong dichroism • High-R.I. glass imitation of tanzanite • Large clam “pearl” • Blue sapphires with unusual color zoning • Spinel with filled cavities 322 Gem News International • Comparison of three historic blue diamonds • Natural yellow diamond with nickel-related optical centers • Gem-quality afghanite • Blue beryl discovery in pg. 319 Canada • Gem-quality corundum from Colombia • Emeralds from Mada- gascar with strong blue/green dichroism • Peruvian blue opal • Interesting pearls from the North American West Coast • “Platinum quartz” from Brazil • Some rare faceted gem materials • Large scapolite from Tanzania • Update on tanzanite mining by AFGEM • Chatoyant glass cabochons from China • New synthetic opal varieties • Plastic imitations of a walrus tusk and a sperm whale tooth • Conference reports 348 Book Reviews 351 Gemological Abstracts 362 2003 Index pg. 332 ost gemologists know that Let us all remember that there is General Electric Co. created nothing inherently wrong with lab- the first industrial-quality oratory-grown products, provided synthetic diamonds in 1955. What they are properly disclosed at each many gemologists don’t know is that stage of the distribution pipeline. the production of polycrystalline thin Ultimately, though, the case for films of synthetic diamond actually synthetic diamonds will not be predates this, beginning in 1952. For played out in the trade per se, but decades, chemical vapor deposition rather in the marketplace and in (CVD) polycrystalline synthetic dia- the mind of the consumer. We all mond has been grown over sub- know that consumer confidence is strates and used in a variety of indus- the key to the success of the dia- trial products. mond industry. Anything that shakes that confidence will shake The lead article in this issue of the market and, inevitably, the Gems & Gemology describes the industry itself. creation of single-crystal synthetic diamonds grown by Apollo Diamond Inc. using a CVD The good news about synthetic diamonds is that, for the last process. At first glance, this doesn’t seem so alarming. After two decades, we have stayed well ahead of the learning all, gem-quality synthetic diamonds grown by the classic curve for identifying them, and I see no reason why this “belt” and BARS (high pressure/high temperature) tech- can’t continue. For much of this time, experts have debated niques have been around for decades, and have been whether diamonds grown synthetically would become com- available commercially (although in very small quantities mercially available in sizes, quantities, and prices that could and sizes and, for the most part, in yellow colors) since the fuel consumer demand for the product. The jury may still be mid-1980’s. Put simply, however, CVD-grown synthetic out on these issues. However, it is inevitable, given the diamond generally is a purer product than commercial syn- technology available today, that the right level of investment thetic diamonds created by high pressure/high temperature and the right long-term commitment to the product will techniques, and the CVD synthetics typically fall on the result in commercially viable gem synthetic diamonds. D-to-Z scale or are “brownies.” In addition, in most cases Indeed, the time for readiness appears to be now. sophisticated analytical equipment must be used to conclu- sively identify the material. After Apollo Diamond begins So what have we learned about synthetic diamonds over commercial production of CVD synthetic diamond in the past half century? We know that, while technology 2004, it will be vital for every practicing gemologist to will provide the innovation necessary to create new and understand the challenges that the material may pose to interesting products, this same technology will help fuel identification. the identification of these products as well. Gemological research laboratories are making every The producer has stated that, initially, 5,000–10,000 carats of effort to keep up with this technology, faceted CVD synthetic diamond will be available. Most of challenging as it may be, and to do every- these goods will be quarters and thirds, but by the end of thing they can to protect the public by 2004, stones as large as a full carat may be on the market. properly identifying and disclosing gem- While larger sizes typically will be identified in a qualified quality synthetic diamonds. laboratory, the fact that most diamonds under a carat are not sold with grading reports is cause for concern. The producers are unequivocal about their insistence on proper disclosure, and all indications to GIA certainly support that premise. But could these goods later be “salted” into parcels of natural dia- monds by unscrupulous hands, fully intending to deceive William E. Boyajian, President their customers? Undoubtedly. Gemological Institute of America EDITORIAL GEMS & GEMOLOGY WINTER 2003 267 GEM-QUALITY SYNTHETIC DIAMONDS GROWN BY A CHEMICAL VAPOR DEPOSITION (CVD) METHOD Wuyi Wang, Thomas Moses, Robert C. Linares, James E. Shigley, Matthew Hall, and James E. Butler Brown-to-gray and near-colorless single-crystal type IIa synthetic diamonds grown using a chemi- cal vapor deposition (CVD) technique by Apollo Diamond Inc. have gemological properties that are distinct from those of both natural diamonds and HPHT-grown synthetic gem diamonds. The tabular crystals typically range up to 1 ct or more and a few millimeters thick, and consist of an overgrowth on a natural or synthetic diamond substrate. Faceted CVD synthetic diamond usually cannot be separated from natural diamond with standard gemological techniques; although when portions of the substrate are still present, an experienced gemologist may be able to recognize dif- ferences in luminescence or color between the overgrowth and substrate. In all cases, however, the CVD synthetic diamonds examined to date could be identified in a gemological laboratory by the combination of a strong orangy red fluorescence seen with the De Beers DiamondView deep- ultraviolet imaging system, a characteristic anomalous birefringence (strain) pattern, and distinctive features in their infrared absorption spectra (e.g., at 3123 cm-1) and photoluminescence spectra (strong 575 and 637 nm emissions, a doublet at 596 and 597 nm, and a line at 737 nm). pollo Diamond Inc. of Boston, Massa- IIa brown diamonds, which can be decolorized at chusetts, has succeeded in growing facetable, high pressure and high temperature (see box A). Asingle-crystal type IIa synthetic diamonds Preliminary notes on GIA’s examination of some of using a patented chemical vapor deposition (CVD) these Apollo samples were published by Wang et al. technique (Linares and Doering, 1999, 2003). For (2003) and appeared in the August 8, 2003 issue of characterization of this material, the company has the GIA Insider (GIA’s electronic newsletter: provided a number of brown-to-gray and near-color- http://www.gia.edu/newsroom/issue/2798/1842/ less gem-quality crystals and faceted samples, which insider_newsletter_details.cfm#3). Spectroscopic represent what is intended to become a commercial analysis of an Apollo CVD synthetic diamond also product for use in high-technology applications as was performed recently by other researchers well as for jewelry purposes (figure 1). Because of the (Deljanin et al., 2003). The purpose of the present growth conditions and mechanisms used, the gemo- article is to provide a more complete description of logical properties of these CVD-produced synthetic this material and its identifying features. diamonds differ from those of both natural diamonds and synthetic diamonds grown at high pressures and temperatures. For the same reasons, the brown col- See end of article for About the Authors and Acknowledgments. oration of CVD synthetic diamonds may not react in GEMS & GEMOLOGY, Vol. 39, No. 4, pp. 268–283. the same way, or as efficiently, as most natural type © 2003 Gemological Institute of America 268 CVD SYNTHETIC DIAMONDS GEMS & GEMOLOGY WINTER 2003 Figure 1. This jewelry is set with CVD synthetic dia- monds from Apollo Diamond Inc. The pendant contains an HPHT-annealed 0.2 ct CVD synthetic diamond with a color equivalent to “K” on the GIA diamond grading scale (sample no. 57687). The 0.31 ct sample (no. 56924) in the ring on the left is equiva- lent to Fancy Dark brown in color. The Fancy Light brown 0.45 ct CVD synthetic dia- mond (no. 57688) in the ring on the right was HPHT annealed, but no change in color was observed (see box A). Composite of photos by Elizabeth Schrader. BACKGROUND • Is resistant to heat, acids, and radiation Synthetic diamonds have been produced by the high • Is a good electrical insulator, but can be doped pressure/high temperature (HPHT) technique since to act as a semiconductor 1955, with the growth of crystals of a size and quality • Is transparent to visible and almost all infrared suitable for jewelry first announced in 1970 radiation (Crowningshield, 1971; Burns and Davies, 1992).
Recommended publications
  • The Dependence of the Sio Bond Length on Structural Parameters in Coesite, the Silica Polymorphs, and the Clathrasils
    American Mineralogist, Volume 75, pages 748-754, 1990 The dependence of the SiO bond length on structural parameters in coesite, the silica polymorphs, and the clathrasils M. B. BOISEN, JR. Department of Mathematics, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, U.S.A. G. V. GIBBS, R. T. DOWNS Department of Geological Sciences, Virginia Polytechnic Institute and State University, Blacksburg, Virginia 24061, U.S.A. PHILIPPE D' ARCO Laboratoire de Geologie, Ecole Normale Superieure, 75230 Paris Cedex OS, France ABSTRACT Stepwise multiple regression analyses of the apparent R(SiO) bond lengths were com- pleted for coesite and for the silica polymorphs together with the clathrasils as a function of the variables};(O), P (pressure), f,(Si), B(O), and B(Si). The analysis of 94 bond-length data recorded for coesite at a variety of pressures and temperatures indicates that all five of these variables make a significant contribution to the regression sum of squares with an R2 value of 0.84. A similar analysis of 245 R(SiO) data recorded for silica polymorphs and clathrasils indicate that only three of the variables (B(O), };(O), and P) make a signif- icant contribution to the regression with an R2 value of 0.90. The distribution of B(O) shows a wide range of values from 0.25 to 10.0 A2 with nearly 80% of the observations clustered between 0.25 and 3.0 A2 and the remaining values spread uniformly between 4.5 and 10.0 A2. A regression analysis carried out for these two populations separately indicates, for the data set with B(O) values less than three, that };(O) B(O), P, and };(Si) are all significant with an R2 value of 0.62.
    [Show full text]
  • Crystalline Silica, Cristobalite (CAS No
    Crystalline Silica, Quartz (CAS No. 14808-60-7) Crystalline Silica, Cristobalite (CAS No. 14464-46-1) Crystalline Silica, Tridymite (CAS No. 15468-32-3) Diatomaceous earth (CAS No. 61790-53-2) This dossier on crystalline silica, quartz, cristobalite and tridymite and diatomaceous earth presents the most critical studies pertinent to the risk assessment of these substances in their use in drilling muds and cement additives. This dossier does not represent an exhaustive or critical review of all available data. The majority of information presented in this dossier was obtained from the ECHA database that provides information on chemicals that have been registered under the EU REACH (ECHA). Where possible, study quality was evaluated using the Klimisch scoring system (Klimisch et al., 1997). For the purpose of this dossier, crystalline silica, quartz (CAS No. 14808-60-7) has been reviewed as representative of crystalline silica cristobalite and tridymite. Crystalline silica, quartz is also considered representative of diatomaceous earth, as they both consist mainly of silicon dioxide. Screening Assessment Conclusion – Crystalline silica, quartz, cristobalite and tridymite and diatomaceous earth are classified as tier 1 chemicals and require a hazard assessment only. 1 BACKGROUND Crystalline silica is a common mineral found in the earth's crust. Materials like sand, stone, concrete and mortar contain crystalline silica. It is also used to make products such as glass, pottery, ceramics, bricks and artificial stone. Silica, in the form of sand, is used as the main ingredient in sand casting for the manufacture of metallic components in engineering and other applications. The high melting point of silica enables it to be used in such applications.
    [Show full text]
  • Pezzottaite from Ambatovita, Madagascar: a New Gem Mineral
    PEZZOTTAITE FROM AMBATOVITA, MADAGASCAR: A NEW GEM MINERAL Brendan M. Laurs, William B. (Skip) Simmons, George R. Rossman, Elizabeth P. Quinn, Shane F. McClure, Adi Peretti, Thomas Armbruster, Frank C. Hawthorne, Alexander U. Falster, Detlef Günther, Mark A. Cooper, and Bernard Grobéty Pezzottaite, ideally Cs(Be2Li)Al2Si6O18, is a new gem mineral that is the Cs,Li–rich member of the beryl group. It was discovered in November 2002 in a granitic pegmatite near Ambatovita in cen- tral Madagascar. Only a few dozen kilograms of gem rough were mined, and the deposit appears nearly exhausted. The limited number of transparent faceted stones and cat’s-eye cabochons that have been cut usually show a deep purplish pink color. Pezzottaite is distinguished from beryl by its higher refractive indices (typically no=1.615–1.619 and ne=1.607–1.610) and specific gravity values (typically 3.09–3.11). In addition, the new mineral’s infrared and Raman spectra, as well as its X-ray diffraction pattern, are distinctive, while the visible spectrum recorded with the spec- trophotometer is similar to that of morganite. The color is probably caused by radiation-induced color centers involving Mn3+. eginning with the 2003 Tucson gem shows, (Be3Sc2Si6O18; Armbruster et al., 1995), and stoppaniite cesium-rich “beryl” from Ambatovita, (Be3Fe2Si6O18; Ferraris et al., 1998; Della Ventura et Madagascar, created excitement among gem al., 2000). Pezzottaite, which is rhombohedral, is Bcollectors and connoisseurs due to its deep purplish not a Cs-rich beryl but rather a new mineral species pink color (figure 1) and the attractive chatoyancy that is closely related to beryl.
    [Show full text]
  • Thermal Behavior of Afghanite, an ABABACAC Member of the Cancrinite Group
    American Mineralogist, Volume 97, pages 630–640, 2012 Thermal behavior of afghanite, an ABABACAC member of the cancrinite group PAOLO BALLIRANO1,2,* AND FERDINANDO BOSI1,3 1Dipartimento di Scienze della Terra, Sapienza Università di Roma, P.le Aldo Moro 5, I-00185, Roma, Italy 2CNR-IGAG, Istituto di Geologia Ambientale e Geoingegneria, Sede di Roma, Via Bolognola 7, I-00138 Roma, Italy 3CNR-IGG Istituto di Geoscienze e Georisorse, Sede di Roma, P.le A. Moro, 5, I-00185 Roma, Italy ABSTRACT Thermal behavior of afghanite, (Na15K5Ca11)Σ31[Si24Al24O96](SO4)6Cl6, P31c, a = 12.7961(7) Å, c = 21.4094(13) Å, an eight-layer member of the cancrinite group, has been investigated by combined electron microprobe analysis, X-ray single-crystal diffraction, and high-temperature X-ray powder diffraction. Non-ambient X-ray powder diffraction data were collected in the 323–1223 K thermal range on a specimen from Case Collina, Latium, Italy. Structural refinement and site assignment based on the bond-valence analysis, performed on room-temperature single-crystal X-ray diffraction data, provided more accurate site allocation of cations than the available model in the literature. The results show that the cancrinite cages alternating with the liottite cages are more compressed along the c-axis than the remaining ones. As a result the chlorine atom, located at the center of the cages, is driven off-axis to release the steric strain due to the cage compression. Thermal expansion shows a discontinuity at 448 K for both a and c unit-cell parameters, a feature previously reported for other cancrinite-like minerals.
    [Show full text]
  • The Red Emerald
    The Red Emerald Black Album Words by Seth William Rozendaal Photos by David Rozendaal This work is for the enjoyment of gemstone aficionados around the world and throughout time, and dedicated to the divine muse who inspires everything. This book celebrates the Red Emerald’s public debut at the 2017 Tucson Gem and Mineral Show. Graphics taken from the Mineralogical Record Volume 47 Number 1: Colombian Emeralds where noted. The two photos of the Heart matrix specimen on the top of the page in Section VI were taken by Wayne Schrimp. Seth Rozendaal is responsible for the landscape photo in Section II, the beveled heart in Section VI and Office Suite Graphics. The Suite Treasure necklace photo in Section XIII was taken at the Brent Isenberger Studio. Cover and all other interior photos in this album were taken by David Rozendaal. Without his tireless dedication, this publication would not have been possible. For additional information, please contact: Seth William Rozendaal (515) 868-7207 [email protected] Index I - Red Beryl IS Red Emerald II - Formation III - Matrix Specimens IV - Wafers V - Prisms VI - Twins VII - Clusters VIII - Bixbyite Combinations IX - Topaz Combinations X - Hourglass Patterning XI - The Scarlet Spectrum XII - Facet-Grade Red Emerald XIII - The Red Emerald Suite Treasure I ~ Red Beryl IS Red Emerald The human infatuation with Emeralds runs so deep, and our desire for them traces so far back… It's one of the only gemstones found in rank-signifying Neolithic headdresses. Yeah, you heard me: Caveman Crowns. Aja Raden - Author, Historian and Scientist Diamonds may be forever, but only Emeralds are eternal; our appreciation of Emeralds stretches from the beginning of human civilization to the very end.
    [Show full text]
  • Washington State Minerals Checklist
    Division of Geology and Earth Resources MS 47007; Olympia, WA 98504-7007 Washington State 360-902-1450; 360-902-1785 fax E-mail: [email protected] Website: http://www.dnr.wa.gov/geology Minerals Checklist Note: Mineral names in parentheses are the preferred species names. Compiled by Raymond Lasmanis o Acanthite o Arsenopalladinite o Bustamite o Clinohumite o Enstatite o Harmotome o Actinolite o Arsenopyrite o Bytownite o Clinoptilolite o Epidesmine (Stilbite) o Hastingsite o Adularia o Arsenosulvanite (Plagioclase) o Clinozoisite o Epidote o Hausmannite (Orthoclase) o Arsenpolybasite o Cairngorm (Quartz) o Cobaltite o Epistilbite o Hedenbergite o Aegirine o Astrophyllite o Calamine o Cochromite o Epsomite o Hedleyite o Aenigmatite o Atacamite (Hemimorphite) o Coffinite o Erionite o Hematite o Aeschynite o Atokite o Calaverite o Columbite o Erythrite o Hemimorphite o Agardite-Y o Augite o Calciohilairite (Ferrocolumbite) o Euchroite o Hercynite o Agate (Quartz) o Aurostibite o Calcite, see also o Conichalcite o Euxenite o Hessite o Aguilarite o Austinite Manganocalcite o Connellite o Euxenite-Y o Heulandite o Aktashite o Onyx o Copiapite o o Autunite o Fairchildite Hexahydrite o Alabandite o Caledonite o Copper o o Awaruite o Famatinite Hibschite o Albite o Cancrinite o Copper-zinc o o Axinite group o Fayalite Hillebrandite o Algodonite o Carnelian (Quartz) o Coquandite o o Azurite o Feldspar group Hisingerite o Allanite o Cassiterite o Cordierite o o Barite o Ferberite Hongshiite o Allanite-Ce o Catapleiite o Corrensite o o Bastnäsite
    [Show full text]
  • Mineral Processing
    Mineral Processing Foundations of theory and practice of minerallurgy 1st English edition JAN DRZYMALA, C. Eng., Ph.D., D.Sc. Member of the Polish Mineral Processing Society Wroclaw University of Technology 2007 Translation: J. Drzymala, A. Swatek Reviewer: A. Luszczkiewicz Published as supplied by the author ©Copyright by Jan Drzymala, Wroclaw 2007 Computer typesetting: Danuta Szyszka Cover design: Danuta Szyszka Cover photo: Sebastian Bożek Oficyna Wydawnicza Politechniki Wrocławskiej Wybrzeze Wyspianskiego 27 50-370 Wroclaw Any part of this publication can be used in any form by any means provided that the usage is acknowledged by the citation: Drzymala, J., Mineral Processing, Foundations of theory and practice of minerallurgy, Oficyna Wydawnicza PWr., 2007, www.ig.pwr.wroc.pl/minproc ISBN 978-83-7493-362-9 Contents Introduction ....................................................................................................................9 Part I Introduction to mineral processing .....................................................................13 1. From the Big Bang to mineral processing................................................................14 1.1. The formation of matter ...................................................................................14 1.2. Elementary particles.........................................................................................16 1.3. Molecules .........................................................................................................18 1.4. Solids................................................................................................................19
    [Show full text]
  • Minnesota's Mineral Resources
    CHAPTER • 9 Minnesota's Mineral Resources IN MINNESOTA the production of iron ore is far more valuable economically than the total of all other mineral products, but im­ portant industries are based on Minnesota's other geological forma­ tions as well. Architectural, monumental, and structural stone are produced from granite, limestone, dolomite, and other Minnesota rocks. Gravel and sand are excavated and processed, and clay is used for many ceramic products. :Manganese in important amounts occurs in the iron ores of the Cuyuna district. Finally, although they are often not thought of as mineral products, two of our most im­ portant mineral resources are water and soil. The iron ores and mining operations of the Mesabi, Vermilion, and Cuyuna iron-bearing districts and of the southeastern lYlinnesota counties will be discussed in detail in later chapters, but a few sta­ tistics on Minnesota's iron ore industry may remind us how impor­ tant this geological heritage is. The following is an estimate of Min­ nesota's iron ore reserves, made on lYlay 1, 1961: Gross Tons Mesabi Range 500,799,179 Vermilion Range 9,755,974 Cuyuna Range 36,530,000 Fillmore County 'il,860,337 Total iron ore 549,945,490 172 MI NESOTA'S MINERAL RESOURCES The total production of iron ore in Minne ota to January 1, 1962, was 2,529,737,553 tons. Total taxes paid on iron ore to January 1, 1961 , were approximately $1,257,448,400, a very important source of funds for the state government. Slightly over 60 per cent of the total iron ore produced in the United States has come from l\1inne- ota.
    [Show full text]
  • Marinellite, a New Feldspathoid of the Cancrinite-Sodalite Group
    Eur. J. Mineral. 2003, 15, 1019–1027 Marinellite, a new feldspathoid of the cancrinite-sodalite group ELENA BONACCORSI* and PAOLO ORLANDI Dipartimento di Scienze della Terra, Universita` di Pisa, Via S. Maria 53, I-56126 Pisa, Italy * Corresponding author, e-mail: [email protected] Abstract: Marinellite, [(Na,K)42Ca6](Si36Al36O144)(SO4)8Cl2·6H2O, cell parameters a = 12.880(2) Å, c = 31.761(6) Å, is a new feldspathoid belonging to the cancrinite-sodalite group. The crystal structure of a twinned crystal was preliminary refined in space group P31c, but space group P62c could also be possible. It was found near Sacrofano, Latium, Italy, associated with giuseppettite, sanidine, nepheline, haüyne, biotite, and kalsilite. It is anhedral, transparent, colourless with vitreous lustre, white streak and Mohs’ hardness of 5.5. The mineral does not fluoresce, is brittle, has conchoidal fracture, and presents poor cleavage on {001}. Dmeas is 3 3 2.405(5) g/cm , Dcalc is 2.40 g/cm . Optically, marinellite is uniaxial positive, non-pleochroic, = 1.495(1), = 1.497(1). The strongest five reflections in the X-ray powder diffraction pattern are [d in Å (I) (hkl)]: 3.725 (100) (214), 3.513 (80) (215), 4.20 (42) (210), 3.089 (40) (217), 2.150 (40) (330). The electron microprobe analysis gives K2O 7.94, Na2O 14.95, CaO 5.14, Al2O3 27.80, SiO2 32.73, SO3 9.84, Cl 0.87, (H2O 0.93), sum 100.20 wt %, less O = Cl 0.20, (total 100.00 wt %); H2O calculated by difference. The corresponding empirical formula, based on 72 (Si + Al), is (Na31.86K11.13Ca6.06) =49.05(Si35.98Al36.02)S=72O144.60(SO4)8.12Cl1.62·3.41H2O.
    [Show full text]
  • Scandiobabingtonite, a New Mineral from the Baveno Pegmatite
    American Mineralogist, Volume 83, pages 1330-1334, 1998 Scandiobabingtonite,a new mineral from the Bavenopegmatite, Piedmont, Italy Ploro ORl.tNnIrr'* Ma,nco PasERorr and GrovlNNa Vn,zzllrNr2 rDipartimento di Scienzedella Terra, Universitd di Pisa, Via S. Maria 53,1-56126 Pisa, Italy '?Dipartimento di Scienzedella Terra, Universitd di Modena, Via S Eufemia 19, I-41 100 Modena, Italy Ansrntcr Scandiobabingtonite,ideally Ca,(Fe,*,Mn)ScSi,O,o(OH) is the scandium analogue of babingtonite; it was found in a pegmatitic cavity of the Baveno granite associatedwith orthoclase, albite, muscovite, stilbite, and fluorite. Its optics are biaxial (+) with 2V : : ^v: 64(2)",ct 1.686(2),P: 1.694(3), 1.709(2).D-"." : 3.24(5)slcm3, D.",.:3.24 sl cm3, and Z : 2. Scandiobabingtoniteis colorless or pale gray-green, transparent,with vitreous luster. It occurs as submillimeter sized, short, tabular crystals, slightly elongated on [001],and characterizedby the associationof forms {010}, {001}, {110}, {110}, and {101}. It occurs also as a thin rim encrustingsmall crystals of babingtonite.The strongest lines in the X-ray powder pauern are at2.969 (S), 2.895 (S), 3.14 (mS), and 2.755 (mS) 4. fn" mineralis triclinic, ipu.. g.oup PT, with a : 7.536(2),b : 1L734(2),c : 6.t48(Z) A, : 91.10(2), : 93.86(2), : lO+.S:(2)'. Scandiobabingtoniteis isostructural " B r with babingtonite, with Sc replacing Fe3* in sixfold coordination, but no substitution of Fer* by Sc takes place. Due to the lack of a suitably large crystal of the new species, such a replacementhas been confirmed by refining the crystal structure of a Sc-rich babingtonite (final R : O.O47)using single-crystal X-ray diffraction (XRD) data.
    [Show full text]
  • 26 May 2021 Aperto
    AperTO - Archivio Istituzionale Open Access dell'Università di Torino The crystal structure of sacrofanite, the 74 Å phase of the cancrinite–sodalite supergroup This is the author's manuscript Original Citation: Availability: This version is available http://hdl.handle.net/2318/90838 since Published version: DOI:10.1016/j.micromeso.2011.06.033 Terms of use: Open Access Anyone can freely access the full text of works made available as "Open Access". Works made available under a Creative Commons license can be used according to the terms and conditions of said license. Use of all other works requires consent of the right holder (author or publisher) if not exempted from copyright protection by the applicable law. (Article begins on next page) 05 October 2021 This Accepted Author Manuscript (AAM) is copyrighted and published by Elsevier. It is posted here by agreement between Elsevier and the University of Turin. Changes resulting from the publishing process - such as editing, corrections, structural formatting, and other quality control mechanisms - may not be reflected in this version of the text. The definitive version of the text was subsequently published in MICROPOROUS AND MESOPOROUS MATERIALS, 147, 2012, 10.1016/j.micromeso.2011.06.033. You may download, copy and otherwise use the AAM for non-commercial purposes provided that your license is limited by the following restrictions: (1) You may use this AAM for non-commercial purposes only under the terms of the CC-BY-NC-ND license. (2) The integrity of the work and identification of the author, copyright owner, and publisher must be preserved in any copy.
    [Show full text]
  • INCLUSIONS in AQUAMARINE from AMBATOFOTSIKELY, MADAGASCAR Fabrice Danet, Marie Schoor, Jean-Claude Boulliard, Daniel R
    NEW Danet G&G Fall 2012_Layout 1 9/27/12 11:31 AM Page 205 RAPID COMMUNICATIONS INCLUSIONS IN AQUAMARINE FROM AMBATOFOTSIKELY, MADAGASCAR Fabrice Danet, Marie Schoor, Jean-Claude Boulliard, Daniel R. Neuville, Olivier Beyssac, and Vincent Bourgoin grams of translucent to transparent beryl were pro- duced, as well as several tonnes of opaque material In January 2012, aquamarine crystals containing for industrial use. While only a very small percentage interesting inclusions were extracted from the Am- was suitable for faceting, several hundred aqua- batofotsikely area northwest of Antsirabe, Mada- marines in the 1–35 ct range have been cut. In April gascar. These specimens displayed various types 2012, one of the authors (FD) traveled to the locality of eye-visible and microscopic inclusions, and and obtained representative samples. some had an unusual form. Raman microspec- troscopy identified reddish brown plate lets as Location and Geologic Setting. The workings are lo- hematite, while ilmenite was found as black cated less than 1 km north of Ambatofotsikely (a village platelets, black needles, and distinctive dark gray now locally known as Ambatofotsy Carole), 22 km dendrites. Similar inclusions are known in beryl north-northwest of Ankazomiriotra, and 74 km north- from Brazil, India, Mozambique, and Sri Lanka. west of Antsirabe. The deposit is centered at coordinates 19°27.662¢S, 46°27.450¢E, at an elevation of 1,010 m. The site is accessed by a paved road (RN 34) from ining activity near the central Malagasy village Antsirabe to a point 16 km west of Ankazomiriotra. of Ambatofotsikely was first documented nearly From there, a trail extends 15 km to Ambatofotsikely.
    [Show full text]