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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. -
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 -
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. -
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. -
Thirty-Fourth List of New Mineral Names
MINERALOGICAL MAGAZINE, DECEMBER 1986, VOL. 50, PP. 741-61 Thirty-fourth list of new mineral names E. E. FEJER Department of Mineralogy, British Museum (Natural History), Cromwell Road, London SW7 5BD THE present list contains 181 entries. Of these 148 are Alacranite. V. I. Popova, V. A. Popov, A. Clark, valid species, most of which have been approved by the V. O. Polyakov, and S. E. Borisovskii, 1986. Zap. IMA Commission on New Minerals and Mineral Names, 115, 360. First found at Alacran, Pampa Larga, 17 are misspellings or erroneous transliterations, 9 are Chile by A. H. Clark in 1970 (rejected by IMA names published without IMA approval, 4 are variety because of insufficient data), then in 1980 at the names, 2 are spelling corrections, and one is a name applied to gem material. As in previous lists, contractions caldera of Uzon volcano, Kamchatka, USSR, as are used for the names of frequently cited journals and yellowish orange equant crystals up to 0.5 ram, other publications are abbreviated in italic. sometimes flattened on {100} with {100}, {111}, {ill}, and {110} faces, adamantine to greasy Abhurite. J. J. Matzko, H. T. Evans Jr., M. E. Mrose, lustre, poor {100} cleavage, brittle, H 1 Mono- and P. Aruscavage, 1985. C.M. 23, 233. At a clinic, P2/c, a 9.89(2), b 9.73(2), c 9.13(1) A, depth c.35 m, in an arm of the Red Sea, known as fl 101.84(5) ~ Z = 2; Dobs. 3.43(5), D~alr 3.43; Sharm Abhur, c.30 km north of Jiddah, Saudi reflectances and microhardness given. -
New Mineral Names*
AmericanMineralogM, Volume66, pages 1099-l103,IgEI NEW MINERAL NAMES* LouIs J. Cetnt, MrcHeer FtnrscHnn AND ADoLF Pnssr Aldermanlter Choloallte. I. R. Harrowficl4 E. R. Segnitand J. A. Watts (1981)Alderman- S. A. Williams (1981)Choloalite, CuPb(TeO3)z .HrO, a ncw min- ite, a ncw magnesiumalrrminum phosphate.Mineral. Mag.44, eral. Miaeral. Mag. 44, 55-51. 59-62. Choloalite was probably first found in Arabia, then at the Mina Aldermanite o@urs as minute, very thin" talc-likc crystallitcs La Oriental, Moctczuma, Sonora (the typc locality), and finally at with iuellite and other secondaryphosphates in the Moculta rock Tombstone, Arizona. Only thc Tombstone material provides para- phosphatc deposit near thc basc of Lower Cambrisn limestone genetic information. In this material choloalite occurs with cerus- close to Angaston, ca. 60 km NE of Adelaide. Microprobc analy- site, emmonsite and rodalquilarite in severcly brecciated shale that si.q supplcmented by gravimetric water determination gave MgO has been replaced by opal and granular jarosite. Wet chcmical E.4,CaO 1.2, AJ2O328.4, P2O5 25.9, H2O 36.1%,(totat 100),lead- analysisofcholoalitc from the type locality gave CuO 11.0,PbO ing to the formula Mg5Als2(POa)s(OH)zz.zH2O,where n = 32. 33.0,TeO2 50.7, H2O 3.4,total 98.1%,correspolding closcly to thc Thc powder diffraction pattern, taken with a Guinier camera, can formula in the titlc. Powder pattems of thc mineral from thc three be indexed on an orthorhombic. ccll with a = 15.000(7), D = localities can bc indexcd on the basis of a cubic ccll with a : 8.330(6),c - 26.60(l)A, Z = 2,D alc.2.15 from assumedcell con- l2.5l9A for the material from Mina La Oriental, Z: l2,D c,alc. -
Bojarite, Found and Characterized by a Research Team Led by Nikita Chukanov (Russian Academy of Sciences, Moscow)
For 2020 the “Mineral of the Year” award has been assigned to bojarite, found and characterized by a research team led by Nikita Chukanov (Russian Academy of Sciences, Moscow). The full description of the new mineral is available here: Chukanov, N.V., Möhn, G., Zubkova, N.V., Ksenofontov, D.A., Pekov, I.V., Agakhanov, A.A., Britvin, S.N., Desor, J. (2020): Bojarite, Cu3(N3C2H2)3(OH)Cl2·6H2O, a new mineral species with a microporous metal-organic framework from the guano deposit at Pabellón de Pica, Iquique Province, Chile. Mineralogical Magazine, 84, 921-927. Bojarite was discovered in a guano deposit on the northern slope of the Pabellón de Pica Mountain, 1.5 km south of Chanabaya village, Iquique Province, Tarapacá Region, Chile. The mineral occurs as blue fine-grained porous aggregates a few mm wide. Associated minerals are salammoniac, halite, chanabayaite, nitratine, and belloite (Fig. 1). Its ideal chemical formula is Cu3(N3C2H2)3(OH)[Cl2(H2O)4]·2H2O, hence bojarite is a copper triazolate mineral. Bojarite crystallizes in the cubic system, and has space group Fd 3c, with a = 24.8047(5) Å. The crystal structure of bojarite has been refined by the Rietveld method and is definitely elegant: three Cu2+ cations are linked by an hydroxyl anion at the center of an equilateral triangle and are also 2+ connected to two nitrogen atoms of the triazole ring, leading to the formation of [Cu3(trz)3(OH)] – building blocks [where trz = 1,2,4-triazole anion (N3C2H2) ]. The third nitrogen atom of the triazole ring connects the triangular unit with adjacent units, giving rise to a three-dimensional network. -
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 -
Italian Type Minerals / Marco E
THE AUTHORS This book describes one by one all the 264 mi- neral species first discovered in Italy, from 1546 Marco E. Ciriotti was born in Calosso (Asti) in 1945. up to the end of 2008. Moreover, 28 minerals He is an amateur mineralogist-crystallographer, a discovered elsewhere and named after Italian “grouper”, and a systematic collector. He gradua- individuals and institutions are included in a pa- ted in Natural Sciences but pursued his career in the rallel section. Both chapters are alphabetically industrial business until 2000 when, being General TALIAN YPE INERALS I T M arranged. The two catalogues are preceded by Manager, he retired. Then time had come to finally devote himself to his a short presentation which includes some bits of main interest and passion: mineral collecting and information about how the volume is organized related studies. He was the promoter and is now the and subdivided, besides providing some other President of the AMI (Italian Micromineralogical As- more general news. For each mineral all basic sociation), Associate Editor of Micro (the AMI maga- data (chemical formula, space group symmetry, zine), and fellow of many organizations and mine- type locality, general appearance of the species, ralogical associations. He is the author of papers on main geologic occurrences, curiosities, referen- topological, structural and general mineralogy, and of a mineral classification. He was awarded the “Mi- ces, etc.) are included in a full page, together cromounters’ Hall of Fame” 2008 prize. Etymology, with one or more high quality colour photogra- geoanthropology, music, and modern ballet are his phs from both private and museum collections, other keen interests. -
C:\Documents and Settings\Alan Smithee\My Documents\MOTM\Lazurite.Wpd
Cdbdladq1//8Lhmdq`knesgdLnmsg9K`ytqhsd From one of the world’s oldest mines in one of the world’s most remote and dangerous localities comes one of the best loved gemstone minerals, straight to your door! Our write-up explains the relationship of lazurite and lapis lazuli, Afghanistan’s legacy of lapis, and the fascinating history of its ancient mines. OVERVIEW PHYSICAL PROPERTIES Chemistry: (Na,Ca)8Si6Al6O24[(SO4),S,Cl,(OH)]2 Basic Sodium Calcium Aluminum Sulfate Chlorosilicate (Sodium Calcium Sulfate Chloroaluminosilicate Hydroxide) Class: Silicates Subclass: Tectosilicates Group: Sodalite Crystal System: Isometric (Cubic) Crystal Habit: Usually dodecahedral, occasionally cubic; most often in granular, compact, or massive form. Color: Azure-blue to violet-blue, occasionally greenish-blue. Luster: Dull to greasy Transparency: Usually opaque; occasionally translucent. Streak: Pale blue Refractive Index: 1.502-1.522 Cleavage: Poor in six directions Fracture: Uneven, brittle Hardness: 5.0-5.5 Specific Gravity: 2.4-2.5 Luminescence: None Distinctive Features and Tests: Best field marks are deep-blue color and association with pyrite [iron disulfide, FeS2]. Can be confused visually with sodalite [sodium aluminum chlorosilicate, Na8Al6Si6O24Cl2], which has coarser grain and paler color, and lazulite [basic magnesium aluminum phosphate, MgAl2(PO4)2(OH)2], which is softer and more dense. Dana Classification Number: 76.2.3.4.1 NAME The name “lazurite,” pronounced LAH-zhur-ite, stems from the Arabic lazaward, variously meaning “sky,” “heaven,” or “azure,” in reference to the mineral’s blue color. Lazurite has also been known as “cyaneus,” “ultramarine,” “lasurite,” “Lasurstein,” “lapis lazuli,” “lapis stone,” “sapphis,” and “sapphirus.” In European mineralogical literature, lazurite appears as lazurit and lazurita. -
Toxicological Profile for Nitrate and Nitrite
NITRATE AND NITRITE 151 4. CHEMICAL AND PHYSICAL INFORMATION 4.1 CHEMICAL IDENTITY Information regarding the chemical identity of nitrate and nitrite is provided in Table 4-1 and information regarding the chemical identity of selected inorganic nitrate and nitrite compounds is provided in Table 4-2. Information regarding ammonia and urea is provided in Table 4-3. Inorganic nitrate and nitrite are naturally occurring ionic species that are part of the earth’s nitrogen cycle (see Figure 5-1). These anions are the products formed via the fixation of nitrogen and oxygen. Chemical processes, biological processes, and microbial processes in the environment convert nitrogen compounds to nitrite and nitrate via nitrogen fixation and nitrification. Compounds such as urea are converted via hydrolysis to ammonia, protonation of ammonia to ammonium (cation), followed by oxidation of ammonium to form nitrite, and then oxidation to form nitrate. Nitrate and nitrite are not neutral compounds, but rather the ionic (anionic; negatively charged) portions of compounds, commonly found in commerce as organic and inorganic salts. As used in this profile, the word “ion” is implied and not used, unless added for clarity. Nitrate and nitrite typically exist in the environment as highly water-soluble inorganic salts, often bound when not solubilized to metal cations such as sodium or potassium. The nitrate ion is the more stable form as it is chemically unreactive in aqueous solution; however, it may be reduced through biotic processes with nitrate reductase to the nitrite ion. The nitrite ion is readily oxidized back to the nitrate ion via Nitrobacter (a genus of proteobacteria), or conversely, the nitrite ion may be reduced to various compounds (IARC 2010; WHO 2011b). -
Volume 66, 1981*
INDEX, VOLUME 66, 1981* Ab jnixio M0 calculations 819,1237 Analyses, cont. Analyses,cont. 'l233 974 Achondrite, oriented olivine ec1og i ie 459 zoisite, Cr epi dote, Cr 974 ANDERS0N,C.S. and S.t^l. BAILEY: ACKERMAND,DIETRICH see pattern FRANZ,GERHARD 872 eugsteri te A newcation ordering 185 Acrofanite, newmineral (abstr) I'r00 fayal i te 95 in amesite-2az Adu.laria,analyses 484 Fe dolomite 51? ANDERSON,J.B. sEeSHOEMAKER, 485 forsteri te 498 G.L. 169 Aegirine, analyses genesis 938 Afghanite, structure 777 fri edeli te I 061 Andesite,experirnental garnet 463,7lI ,743,1027 Anilite, Cu-Sbond 813 Ajoite, newdata 201 phase AKIZUKI,MIZUHIK0: Investigation glasses, Na 547 Anorthite, equilibria ll83 of phase transition of natural graphitic sulfidic schists 916 Antaractica greenali te az5 meteoriticolivine I 233 ZnSminerals by high resolu- '1006 to22 tion electron microscopy halloysite r 004 surinamite,etc. 480 Antigorite, dissolution 801 _: Origin of optical heulandi te variation in analcime 403 hypersthene 75,337 Apatite Albi te i I menite 95,728,978 analyses 670 analys es 484 iron formation 89,51 1 inclusionin Cr diopside 347 heat capacity 1202 jonsomervilleite 834 Apuanite, microstructure I 073 Aldermanite,new mineral (abstr) 1099 kanoite 128 Aragonite,oolite 789 ARAKI.TAKAHARU and P.B. M00RE: Alforsite, newmineral 1050 kaolinite rock I 004 - Alkali diffusion, EPMA 547 kar'l i te 875 Diieni te, cul+Mn?tFe3l(oH)6 kornerupine 743 (Asrt03)5(Si lr04J i(Asr+04 ) : Alkali feldspars, thennodynamic t+; functi ons 1202 kutnahorite 280 metallic (AslrCu clusters Alkremite, Utah 741 kyani te 706 in an oxide matrix 1263 ALLARD,L.F.