Stability and Solubility of Carbonate Minerals of Divalent Cations the Plot Below Shows the Thermodynamic Stability, Mineral Groups

Total Page:16

File Type:pdf, Size:1020Kb

Stability and Solubility of Carbonate Minerals of Divalent Cations the Plot Below Shows the Thermodynamic Stability, Mineral Groups Railsback's Some Fundamentals of Mineralogy and Geochemistry Stability and solubility of carbonate minerals of divalent cations The plot below shows the thermodynamic stability, mineral groups. For example, calcite is more solu- These facts help account for many of the and thus the solubility, of some carbonate minerals of ble than otavite, siderite, rhodochrosite, and interesting issues of carbonate petrology: #3 for why divalent cations. Blue is used to highlight the smithsonite, and aragonite is more soluble than waters may precipitate one CaCO3 mineral under rhombohedral carbonate minerals like calcite, where strontianite and cerussite. certain conditions but another CaCO3 mineral under 2+ 2+ the inter-radical cation (e.g., Ca in calcite) is nested 5) The two most abundant 2+ cations, Ca and other conditions; #4 for why both of the CaCO3 among six O2- anions. Red is used to highlight the Mg2+, fall outside the rhomobohdral and ortho- minerals are so soluble, giving us both caves and orthorhombic carbonates like aragonite, where the rhombic windows and therefore form relatively speleothems; and #5 and #6 for why dolomitization is inter-radical cation (e.g., Ca2+ in aragonite) is nested soluble carbonate minerals. so common and the dolomite problem so important. in a larger cation site among nine oxygens. 6) A mineral of two cations at the ends of a group is It would be a much less interesting world if our Things to note include more stable than the minerals of single cations. carbonate deposits consisted of carbonates of Cd2+ 1) Smaller cations make rhombohedral carbonate For example, dolomite is more stable than mag- or Pb2+ and thus did not offer so much mineralogical minerals, and larger cations form orthorhombic nesite and calcite, and alstonite is more stable than variablilty and such susceptibility to dissolution, carbonate minerals, as one would expect from the aragonite and witherite. reprecipitation, and diagenetic alteration. difference in coordination. 2) Within each group, cations -80 -14 with radii near the middle of Orthorhombic Carbonate their respective group form Window LEGEND Cations less soluble, and thus more -75 Rhombohedral Carbonate -13 One Two 2+ stable, minerals. Fe in Window Rhombohedral 2+ Cerussite Carbonates siderite and Cd in otavite (six-fold coord'n) Stable -70 Otavite2 luble are examples among the -12 Orthorhombic rhombohedral carbonate Ankerite Carbonates minerals. On the other hand, 1 (nine-fold coord'n) 2 Otavite More cations at the end of each -65 Rhodochrosite Hexagonal range are more soluble. Mg2+ -11 So More Carbonates in magnesite and Ca2+ in Siderite Hydrous G) of formation G) of -60 calcite are examples among Carbonates ∆ Smith- 2 the rhombohedral carbonate sonite Dolomite -10 minerals. These observa- -55 Sphaero- tions define the two "windows" cobaltite Stron- Alstonite Ksp is the solubility of greater stabilitiy in the tianite Dolomite 1 -9 product, the equilibrium diagram. -50 Calcite 25°C at constant for dissolution 2+ sp 3) Ca falls at the boundary Mag- from ions at 25°C (kJ/mol) 25°C at from ions or precipitation. For between the rhombohedral nesite Aragonite -8 and orthorhombic carbonate Free ( Energy -45 Vaterite example, for CaCO3 minerals, accounting for the Monohydrocalcite Log K 2+ 2- Mg-Calcites Witherite Ksp = aCa x aCO3 . existence of two common (CaCO3•H20) -40 -7 The results shown were calculated from data in polymorphs of CaCO3, calcite Ikaite (CaCO3•6H20) and aragonite. Gaspéite Robie et al. (1979), except for dolomite2, ankerite, and alstonite from Garrels et al. (1960); gaspéite, 4) The two most common Mg calcites and hydrous carbonates from Table 2.1 carbonate minerals, calcite -30 Nesquehonite (MgCO3•3H20) of Morse and MacKenzie (1990); rhodochrosite2 and aragonite, are both more -5 from Wartel et al. (1990); and otavite2 from Stipp et al. (1993). Log Ksp values for carbonates of two soluble than minerals of other cations (e.g., dolomite) were halved to convert to a 2+ 0.70.8 0.9 1.0 1.1 1.2 1.3 1.4 1.5 cations because Ca falls per-mole-CO3 basis. Data from Tareen et al. (1991) and Fazeli et al. (1991) would suggest an upward outside the windows of the two Cation Radius (Å) LBR CarbMinsvRadii07 Originally published in Car- bonates and Evaporites in 1999. Revised 8/2010. shift of points on the plot but little relative change..
Recommended publications
  • Download PDF About Minerals Sorted by Mineral Name
    MINERALS SORTED BY NAME Here is an alphabetical list of minerals discussed on this site. More information on and photographs of these minerals in Kentucky is available in the book “Rocks and Minerals of Kentucky” (Anderson, 1994). APATITE Crystal system: hexagonal. Fracture: conchoidal. Color: red, brown, white. Hardness: 5.0. Luster: opaque or semitransparent. Specific gravity: 3.1. Apatite, also called cellophane, occurs in peridotites in eastern and western Kentucky. A microcrystalline variety of collophane found in northern Woodford County is dark reddish brown, porous, and occurs in phosphatic beds, lenses, and nodules in the Tanglewood Member of the Lexington Limestone. Some fossils in the Tanglewood Member are coated with phosphate. Beds are generally very thin, but occasionally several feet thick. The Woodford County phosphate beds were mined during the early 1900s near Wallace, Ky. BARITE Crystal system: orthorhombic. Cleavage: often in groups of platy or tabular crystals. Color: usually white, but may be light shades of blue, brown, yellow, or red. Hardness: 3.0 to 3.5. Streak: white. Luster: vitreous to pearly. Specific gravity: 4.5. Tenacity: brittle. Uses: in heavy muds in oil-well drilling, to increase brilliance in the glass-making industry, as filler for paper, cosmetics, textiles, linoleum, rubber goods, paints. Barite generally occurs in a white massive variety (often appearing earthy when weathered), although some clear to bluish, bladed barite crystals have been observed in several vein deposits in central Kentucky, and commonly occurs as a solid solution series with celestite where barium and strontium can substitute for each other. Various nodular zones have been observed in Silurian–Devonian rocks in east-central Kentucky.
    [Show full text]
  • Barite (Barium)
    Barite (Barium) Chapter D of Critical Mineral Resources of the United States—Economic and Environmental Geology and Prospects for Future Supply Professional Paper 1802–D U.S. Department of the Interior U.S. Geological Survey Periodic Table of Elements 1A 8A 1 2 hydrogen helium 1.008 2A 3A 4A 5A 6A 7A 4.003 3 4 5 6 7 8 9 10 lithium beryllium boron carbon nitrogen oxygen fluorine neon 6.94 9.012 10.81 12.01 14.01 16.00 19.00 20.18 11 12 13 14 15 16 17 18 sodium magnesium aluminum silicon phosphorus sulfur chlorine argon 22.99 24.31 3B 4B 5B 6B 7B 8B 11B 12B 26.98 28.09 30.97 32.06 35.45 39.95 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 potassium calcium scandium titanium vanadium chromium manganese iron cobalt nickel copper zinc gallium germanium arsenic selenium bromine krypton 39.10 40.08 44.96 47.88 50.94 52.00 54.94 55.85 58.93 58.69 63.55 65.39 69.72 72.64 74.92 78.96 79.90 83.79 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 rubidium strontium yttrium zirconium niobium molybdenum technetium ruthenium rhodium palladium silver cadmium indium tin antimony tellurium iodine xenon 85.47 87.62 88.91 91.22 92.91 95.96 (98) 101.1 102.9 106.4 107.9 112.4 114.8 118.7 121.8 127.6 126.9 131.3 55 56 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 cesium barium hafnium tantalum tungsten rhenium osmium iridium platinum gold mercury thallium lead bismuth polonium astatine radon 132.9 137.3 178.5 180.9 183.9 186.2 190.2 192.2 195.1 197.0 200.5 204.4 207.2 209.0 (209) (210)(222) 87 88 104 105 106 107 108 109 110 111 112 113 114 115 116
    [Show full text]
  • Selective Flotation of Witherite from Calcite Using Potassium Chromate As a Depressant
    Physicochem. Probl. Miner. Process., 55(2), 2019, 565-574 Physicochemical Problems of Mineral Processing ISSN 1643-1049 http://www.journalssystem.com/ppmp © Wroclaw University of Science and Technology Received May 31, 2018; reviewed; accepted September 2, 2018 Selective flotation of witherite from calcite using potassium chromate as a depressant Yangshuai Qiu 1, Lingyan Zhang 1,2, Xuan Jiao 1, Junfang Guan 1,2, Ye Li 1,2, Yupeng Qian 1,2 1 School of Resources and Environmental Engineering, Wuhan University of Technology, Wuhan 430070, China 2 Hubei Key Laboratory of Mineral Resources Processing & Environment, Wuhan 430070, China Corresponding author: [email protected] (Lingyan Zhang) Abstract: Witherite has been widely used as an industrial and environmental source of barium, with calcite being the primary associated carbonate mineral. However, few studies have been conducted to effectively concentrate witherite from barium ores. In this work, with the treatment of potassium chromate (K2CrO4) and sodium oleate (NaOL), witherite was selectively separated from calcite through selective flotation at different pH conditions. In addition, contact angle, Zeta potential, adsorption and X-ray photoelectron spectroscopy measurements were performed to characterize the separation mechanisms. The results demonstrated that NaOL had a strong collecting ability for both witherite and calcite; nevertheless, witherite could be effectively selected from calcite with the highest recovery at pH 9 in the presence of K2CrO4. From the XPS measurements, NaOL and K2CrO4 were found to be primarily attached to the surfaces of witherite and calcite through chemisorption. The presence of K2CrO4 on the surface of calcite adversely influenced the NaOL adsorption, which could make the flotation separation efficient and successful.
    [Show full text]
  • Infrare D Transmission Spectra of Carbonate Minerals
    Infrare d Transmission Spectra of Carbonate Mineral s THE NATURAL HISTORY MUSEUM Infrare d Transmission Spectra of Carbonate Mineral s G. C. Jones Department of Mineralogy The Natural History Museum London, UK and B. Jackson Department of Geology Royal Museum of Scotland Edinburgh, UK A collaborative project of The Natural History Museum and National Museums of Scotland E3 SPRINGER-SCIENCE+BUSINESS MEDIA, B.V. Firs t editio n 1 993 © 1993 Springer Science+Business Media Dordrecht Originally published by Chapman & Hall in 1993 Softcover reprint of the hardcover 1st edition 1993 Typese t at the Natura l Histor y Museu m ISBN 978-94-010-4940-5 ISBN 978-94-011-2120-0 (eBook) DOI 10.1007/978-94-011-2120-0 Apar t fro m any fair dealin g for the purpose s of researc h or privat e study , or criticis m or review , as permitte d unde r the UK Copyrigh t Design s and Patent s Act , 1988, thi s publicatio n may not be reproduced , stored , or transmitted , in any for m or by any means , withou t the prio r permissio n in writin g of the publishers , or in the case of reprographi c reproductio n onl y in accordanc e wit h the term s of the licence s issue d by the Copyrigh t Licensin g Agenc y in the UK, or in accordanc e wit h the term s of licence s issue d by the appropriat e Reproductio n Right s Organizatio n outsid e the UK. Enquirie s concernin g reproductio n outsid e the term s state d here shoul d be sent to the publisher s at the Londo n addres s printe d on thi s page.
    [Show full text]
  • Conservation of Coated and Specialty Papers
    RELACT HISTORY, TECHNOLOGY, AND TREATMENT OF SPECIALTY PAPERS FOUND IN ARCHIVES, LIBRARIES AND MUSEUMS: TRACING AND PIGMENT-COATED PAPERS By Dianne van der Reyden (Revised from the following publications: Pigment-coated papers I & II: history and technology / van der Reyden, Dianne; Mosier, Erika; Baker, Mary , In: Triennial meeting (10th), Washington, DC, 22-27 August 1993: preprints / Paris: ICOM , 1993, and Effects of aging and solvent treatments on some properties of contemporary tracing papers / van der Reyden, Dianne; Hofmann, Christa; Baker, Mary, In: Journal of the American Institute for Conservation, 1993) ABSTRACT Museums, libraries, and archives contain large collections of pigment-coated and tracing papers. These papers are produced by specially formulated compositions and manufacturing procedures that make them particularly vulnerable to damage as well as reactive to solvents used in conservation treatments. In order to evaluate the effects of solvents on such papers, several research projects were designed to consider the variables of paper composition, properties, and aging, as well as type of solvent and technique of solvent application. This paper summarizes findings for materials characterization, degradative effects of aging, and some effects of solvents used for stain reduction, and humidification and flattening, of pigment-coated and modern tracing papers. Pigment-coated papers have been used, virtually since the beginning of papermaking history, for their special properties of gloss and brightness. These properties, however, may render coated papers more susceptible to certain types of damage (surface marring, embedded grime, and stains) and more reactive to certain conservation treatments. Several research projects have been undertaken to characterize paper coating compositions (by SEM/EDS and FTIR) and appearance properties (by SEM imaging of surface structure and quantitative measurements of color and gloss) in order to evaluate changes that might occur following application of solvents used in conservation treatments.
    [Show full text]
  • List of Abbreviations
    List of Abbreviations Ab albite Cbz chabazite Fa fayalite Acm acmite Cc chalcocite Fac ferroactinolite Act actinolite Ccl chrysocolla Fcp ferrocarpholite Adr andradite Ccn cancrinite Fed ferroedenite Agt aegirine-augite Ccp chalcopyrite Flt fluorite Ak akermanite Cel celadonite Fo forsterite Alm almandine Cen clinoenstatite Fpa ferropargasite Aln allanite Cfs clinoferrosilite Fs ferrosilite ( ortho) Als aluminosilicate Chl chlorite Fst fassite Am amphibole Chn chondrodite Fts ferrotscher- An anorthite Chr chromite makite And andalusite Chu clinohumite Gbs gibbsite Anh anhydrite Cld chloritoid Ged gedrite Ank ankerite Cls celestite Gh gehlenite Anl analcite Cp carpholite Gln glaucophane Ann annite Cpx Ca clinopyroxene Glt glauconite Ant anatase Crd cordierite Gn galena Ap apatite ern carnegieite Gp gypsum Apo apophyllite Crn corundum Gr graphite Apy arsenopyrite Crs cristroballite Grs grossular Arf arfvedsonite Cs coesite Grt garnet Arg aragonite Cst cassiterite Gru grunerite Atg antigorite Ctl chrysotile Gt goethite Ath anthophyllite Cum cummingtonite Hbl hornblende Aug augite Cv covellite He hercynite Ax axinite Czo clinozoisite Hd hedenbergite Bhm boehmite Dg diginite Hem hematite Bn bornite Di diopside Hl halite Brc brucite Dia diamond Hs hastingsite Brk brookite Dol dolomite Hu humite Brl beryl Drv dravite Hul heulandite Brt barite Dsp diaspore Hyn haiiyne Bst bustamite Eck eckermannite Ill illite Bt biotite Ed edenite Ilm ilmenite Cal calcite Elb elbaite Jd jadeite Cam Ca clinoamphi- En enstatite ( ortho) Jh johannsenite bole Ep epidote
    [Show full text]
  • Barite–Celestine Geochemistry and Environments of Formation Jeffrey S
    Barite–Celestine Geochemistry and Environments of Formation Jeffrey S. Hanor Department of Geology and Geophysics Louisiana State University Baton Rouge, Louisiana 70803 INTRODUCTION Minerals in the barite (BaSO4)–celestine (SrSO4) solid solution series, (Ba,Sr)SO4, occur in a remarkably diverse range of sedimentary, metamorphic, and igneous geological environments which span geological time from the Early Archean (~3.5 Ga) to the present. The purpose of this chapter is to review: (1) the controls on the chemical and isotopic composition of barite and celestine and (2) the geological environments in which these minerals form. Some health risks are associated with barite, and these are discussed near the end of this chapter. Although complete solid solution exists between BaSO4 and SrSO4 most representa- tives of the series are either distinctly Ba-rich or Sr-rich. Hence, it is convenient to use the term barite to refer to not only the stochiometric BaSO4 endmember but also to those (Ba,Sr)SO4 solid solutions dominated by Ba. Similarly, the term celestine will refer here not only to the stoichiometric SrSO4 endmember but to solid solutions dominated by Sr. Such usage is in accord with standard mineral nomenclature. The Committee on Mineral Names and Nomenclature of the International Mineralogical Association recognizes “celestine” as the official name for SrSO4. However, the name “celestite” is still commonly used in the literature. Geological significance of barite and celestine Most of the barite which exists in the Earth’s crust has formed through the mixing of fluids, one containing Ba leached from silicate minerals, and the other an oxidized shallow fluid, such as seawater, which contains sulfate.
    [Show full text]
  • Alphabetical List
    LIST L - MINERALS - ALPHABETICAL LIST Specific mineral Group name Specific mineral Group name acanthite sulfides asbolite oxides accessory minerals astrophyllite chain silicates actinolite clinoamphibole atacamite chlorides adamite arsenates augite clinopyroxene adularia alkali feldspar austinite arsenates aegirine clinopyroxene autunite phosphates aegirine-augite clinopyroxene awaruite alloys aenigmatite aenigmatite group axinite group sorosilicates aeschynite niobates azurite carbonates agate silica minerals babingtonite rhodonite group aikinite sulfides baddeleyite oxides akaganeite oxides barbosalite phosphates akermanite melilite group barite sulfates alabandite sulfides barium feldspar feldspar group alabaster barium silicates silicates albite plagioclase barylite sorosilicates alexandrite oxides bassanite sulfates allanite epidote group bastnaesite carbonates and fluorides alloclasite sulfides bavenite chain silicates allophane clay minerals bayerite oxides almandine garnet group beidellite clay minerals alpha quartz silica minerals beraunite phosphates alstonite carbonates berndtite sulfides altaite tellurides berryite sulfosalts alum sulfates berthierine serpentine group aluminum hydroxides oxides bertrandite sorosilicates aluminum oxides oxides beryl ring silicates alumohydrocalcite carbonates betafite niobates and tantalates alunite sulfates betekhtinite sulfides amazonite alkali feldspar beudantite arsenates and sulfates amber organic minerals bideauxite chlorides and fluorides amblygonite phosphates biotite mica group amethyst
    [Show full text]
  • A Specific Gravity Index for Minerats
    A SPECIFICGRAVITY INDEX FOR MINERATS c. A. MURSKyI ern R. M. THOMPSON, Un'fuersityof Bri.ti,sh Col,umb,in,Voncouver, Canad,a This work was undertaken in order to provide a practical, and as far as possible,a complete list of specific gravities of minerals. An accurate speciflc cravity determination can usually be made quickly and this information when combined with other physical properties commonly leads to rapid mineral identification. Early complete but now outdated specific gravity lists are those of Miers given in his mineralogy textbook (1902),and Spencer(M,i,n. Mag.,2!, pp. 382-865,I}ZZ). A more recent list by Hurlbut (Dana's Manuatr of M,i,neral,ogy,LgE2) is incomplete and others are limited to rock forming minerals,Trdger (Tabel,l,enntr-optischen Best'i,mmungd,er geste,i,nsb.ildend,en M,ineral,e, 1952) and Morey (Encycto- ped,iaof Cherni,cal,Technol,ogy, Vol. 12, 19b4). In his mineral identification tables, smith (rd,entifi,cati,onand. qual,itatioe cherai,cal,anal,ys'i,s of mineral,s,second edition, New york, 19bB) groups minerals on the basis of specificgravity but in each of the twelve groups the minerals are listed in order of decreasinghardness. The present work should not be regarded as an index of all known minerals as the specificgravities of many minerals are unknown or known only approximately and are omitted from the current list. The list, in order of increasing specific gravity, includes all minerals without regard to other physical properties or to chemical composition. The designation I or II after the name indicates that the mineral falls in the classesof minerals describedin Dana Systemof M'ineralogyEdition 7, volume I (Native elements, sulphides, oxides, etc.) or II (Halides, carbonates, etc.) (L944 and 1951).
    [Show full text]
  • Definition of a Mineral Each Mineral Species Has Unique and Identifiable Physical Properties. Form and Habit Terms (Crystal Grow
    Definition of a Mineral • A mineral is a naturally occurring, • homogeneous solid with a Physical Properties of Minerals • definite, but not fixed, composition, and Color, shape, density, • an ordered atomic arrangement that is hardness, etc • formed by inorganic processes. • A mineral is a natural, crystalline phase. Form and Habit Terms Each mineral species has (Crystal Growth Forms) unique and identifiable • Prismatic (well developed prism physical properties. faces) (Pyramidal) • Form and habit (Shape) • Columnar (Irregular prism faces) • Luster • Acicular (needle-like) • Color and Streak • Botryoidal (rounded growth surface) • Cleavage and Fracture • Tabular (Platey) • Hardness • Stellate (Radiating) • Density • Fibrous (fibers, asbestiform) • Tenacity • Dendritic (tree-like) Acicular Fibrous 1 Dendritic Dendritic Radiating Radiating Bladed Botryoidal 2 Prismatic Luster and Transparency • Luster • Transparency – Metallic – Opaque – Resinous – Translucent (waxy) – Transparent – Pearly – Greasy – Adamantine – Vitreous Metallic Adamantine Color and Streak • The reflectance color of minerals is strongly affected by transition metals (V, Cr, Mn, Fe, Co, Ni, and Cu). (Also rare earths) Vitreous Pearly • Color in hand specimen may not be diagnostic. • Color in streak generally indicates presence of iron or other transition metals. Chatoyance, Asterism, Asterism: Star Sapphire and Luminescence • Chatoyance and asterism are optical effects due to diffraction of light from small inclusions. • Luminescence is emission of light. – Visible or UV (black light) – Tribo-luminescence: glow when rubbed – Cathodo-luminescence is emission of light from electron bombardment 3 Cleavage and Fracture Hardness What scratches what? • Crystals tend to break on planes of • 1. Talc 6. Orthoclase weakness. • 2. Gypsum 7. Quartz – Cleavage: perfect – Parting: irregular • 3. Calcite 8. Topaz – Hackly: very irregular • 4. Fluorite 9.
    [Show full text]
  • Chemical Staining Methods Used in the Identification of Carbonate Minerals
    CHEMICAL STAINING METHODS USED IN THE IDENTIFICATION OF CARBONATE MINERALS Tamer AYAN Mineral Research and Exploration Institute of Turkey INTRODUCTION Carbonate minerals are the major constituents of sedimentary rocks; however, they are also found in igneous and metamorphic rocks, either as primary or as secondary minerals. In carbonate rocks formed either by chemical or mechanical deposition, these minerals constitute the main rock-forming components. Sometimes they are also found in great abundance in pelitic, psammitic and psephitic rocks. According to their crystallographic characteristics, carbonate minerals may be subdivided into two main groups : 1) Calcite group : Hexagonal-rhombohedral system. 2) Aragonite group : Orthorhombic system «pseudohexagonal». Of the calcite group of minerals, calcite (CaCO3) and dolomite [CaMg (CO3)2] are the two minerals which are dominantly found in sediments. Depending on its purity, or iron and magnesium content, calcite may be found in states of pure calcite, ferro-calcite, or slightly to abundantly magnesian calcite. Similarly, according to the iron content percentage, dolomite may also be regarded as having been composed of two end members, pure dolomite and ferrous dolomite, in varying proportions. The other calcite group minerals are ankerite «ferroferric dolomite» [CaFe(CO3)2], magnesite (MgCO3), siderite (FeCO3), smithsonite (ZnCO3), rhodochrosite (MnCO3) and spherocobaltite (CoC03). The most important mineral of the aragonite group is aragonite (CaCO3); the others, in decreasing order of importance, are witherite (BaCO3), strontianite (SrCO3), cerussite (PbCO3) and alstonite [(Ba, Ca)CO3]. Apart from their refractive indexes (R.I.), the optical and crystallographic characteristics of carbonate minerals are very similar to each other. Therefore identification of carbonates on hand specimens or even in thin sections, is rather difficult.
    [Show full text]
  • The Crystal Structure of Alstonite, Baca(CO3)2: an Extraordinary Example of ‘Hidden’ Complex Twinning in Large Single Crystals
    Mineralogical Magazine (2020), 84, 699–704 doi:10.1180/mgm.2020.61 Article The crystal structure of alstonite, BaCa(CO3)2: an extraordinary example of ‘hidden’ complex twinning in large single crystals Luca Bindi1* , Andrew C. Roberts2 and Cristian Biagioni3 1Dipartimento di Scienze della Terra, Università di Firenze, Via G. La Pira 4, I-50121 Firenze, Italy; 2Geological Survey of Canada, 601 Booth Street, Ottawa, Ontario K1A 0E8, Canada; and 3Dipartimento di Scienze della Terra, Università di Pisa, Via S. Maria 53, I-56126 Pisa, Italy Abstract Alstonite, BaCa(CO3)2, is a mineral described almost two centuries ago. It is widespread in Nature and forms magnificent cm-sized crystals. Notwithstanding, its crystal structure was still unknown. Here, we report the crystal-structure determination of the mineral and discuss it in relationship to other polymorphs of BaCa(CO3)2. Alstonite is trigonal, space group P31m, with unit-cell parameters 3 a = 17.4360(6), c = 6.1295(2) Å, V = 1613.80(9) Å and Z = 12. The crystal structure was solved and refined to R1 = 0.0727 on the σ c basis of 4515 reflections with Fo >4 (Fo) and 195 refined parameters. Alstonite is formed by the alternation, along , of Ba-dominant and Ca-dominant layers, separated by CO3 groups parallel to {0001}. The main take-home message is to show that not all structure determinations of minerals/compounds can be solved routinely. Some crystals, even large ones displaying excellent diffraction quality, can be twinned in complex ways, thus making their study a crystallographic challenge. Keywords: alstonite, carbonate, barium, calcium, crystal structure, twinning (Received 11 June 2020; accepted 25 July 2020; Accepted Manuscript published online: 29 July 2020; Associate Editor: Charles A Geiger) Introduction b = 17.413(5), c = 6.110(1) Å and β = 90.10(1)°, with a unit-cell volume 12 times larger than the orthorhombic cell proposed by Alstonite, BaCa(CO ) , is polymorphous with barytocalcite, para- 3 2 Gossner and Mussgnug (1930).
    [Show full text]