On Laurionite and Associated Minerals from Cornwall
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Paralaurionite Pbcl(OH) C 2001-2005 Mineral Data Publishing, Version 1
Paralaurionite PbCl(OH) c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. Crystals are thin to thick tabular k{100}, or elongated along [001], to 3 cm; {100} is usually dominant, but may show many other forms. Twinning: Almost all crystals are twinned by contact on {100}. Physical Properties: Cleavage: {001}, perfect. Tenacity: Flexible, due to twin gliding, but not elastic. Hardness = Soft. D(meas.) = 6.05–6.15 D(calc.) = 6.28 Optical Properties: Transparent to translucent. Color: Colorless, white, pale greenish, yellowish, yellow-orange, rarely violet; colorless in transmitted light. Luster: Subadamantine. Optical Class: Biaxial (–). Pleochroism: Noted in violet material. Orientation: Y = b; Z ∧ c =25◦. Dispersion: r< v,strong. Absorption: Y > X = Z. α = 2.05(1) β = 2.15(1) γ = 2.20(1) 2V(meas.) = Medium to large. Cell Data: Space Group: C2/m. a = 10.865(4) b = 4.006(2) c = 7.233(3) β = 117.24(4)◦ Z=4 X-ray Powder Pattern: Laurium, Greece. 5.14 (10), 3.21 (10), 2.51 (9), 2.98 (7), 3.49 (6), 2.44 (6), 2.01 (6) Chemistry: (1) (2) (3) Pb 78.1 77.75 79.80 O [3.6] 6.00 3.08 Cl 14.9 12.84 13.65 H2O 3.4 3.51 3.47 insol. 0.09 Total [100.0] 100.19 100.00 (1) Laurium, Greece. (2) Tiger, Arizona, USA. (3) PbCl(OH). Polymorphism & Series: Dimorphous with laurionite. Occurrence: A secondary mineral formed through alteration of lead-bearing slag by sea water or in hydrothermal polymetallic mineral deposits. -
Its Crystal Structure and Relationship to A-Pbf2
American Mineralogist, Volume 81, pages 1277-1281, 1996 Laurelite: Its crystal structure and relationship to a-PbF2 STEFANO MERLINO,! MARCO PASERO,! NATALE PERCHIAZZI,! AND ANrHONY R. KAMPF2 lDipartimento di Scienze della Terra, UniversitA di Pisa, via S. Maria 53, 1-56126 Pisa, Italy 2Mineralogy Section, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, California 90007, U.S.A. ABSTRACT Laurelite, Pb7F12CI2, from the Grand Reefmine, Graham County, Arizona, is hexagonal, Po, with a = 10.267(1) and c = 3.9844(4) A and Z = 1. The crystal structure was solved by direct methods and refined to R = 0.035 and RW2= 0.089 for 693 measured reflections (Fo > 9O'Fo)' The structure is related to that of a-PbF2. Both are based upon ninefold-coordinated Pb as tricapped trigonal prisms (TCTPs), which share edges and faces. The two structures can be described with respect to the face-sharing linkages of their TCTPs. The structure of a-PbF2 consists of corrugated sheets of face-sharing TCTPs that interlock by edge-sharing perpendicular to the c axis. In laurelite, the Pb2 TCTPs form three-membered face-sharing clusters about the threefold axis that are propagated into trigonal cylinders by sharing faces in the direction of the c axis. The Pb 1 and Pb3 TCTPs are linked by face-sharing into a three-dimensional framework with corresponding cylindrical voids. Asymmetric coordi- nations about Pbl and Pb2 are attributed to the stereoactive lone-pair effect. Although the coordinations about the anions appear to disallow substitution of OH for F, stacking defects along the c axis provide a mechanism for accommodating limited OH or H20 for F substitution. -
An Improved Approach to Crystal Symmetry and the Derivation And
71-22,530 SHANKLIN, Robert Elstone, 1915- AN IMPROVED APPROACH TO CRYSTAL SYMMETRY AND THE DERIVATION AND DESCRIPTION OF THE THIRTY- TWO CRYSTAL CLASSES BY MEANS OF THE STEREOGRAPHIC PROJECTION AND GROUP THEORY. The Ohio State University, Ph.D., 1971 Mineralogy University Microfilms, A XEROX Company , Ann Arbor, Michigan ©Copyright by Robert Elstone Shanklin 1971 AN IMPROVED APPROACH TO CRYSTAL SYMMETRY AND THE DERIVATION AND DESCRIPTION OF THE THIRTY-TNO CRYSTAL CLASSES BY MEANS OF THE STEREOGRA.PHIC PROJECTION AND GROUP THEORY DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Robert Elstone Shanklin, A. B., M.S ★ * * * * Approved By Department of Mineralogy PLEASE NOTE: Some pages have indistinct print. Filmed as received. UNIVERSITY MICROFILMS. PREFACE The subject of order in the natural world is a favorite topic of scientists and philosophers alike. If there is any order in the universe, the crystalline state seems to be an excellent place to find it. That which is orderly should be comprehensible. There is no reason why a subject as rich in educational value, as reward ing in intellectual content, and as full of aesthetic satisfaction as crystallography should remain behind a veil of obscurity, the property of a few specialists. As a teacher of crystallography and mineralogy for many years, it has become apparent to me that existing textbooks often do not serve the needs of either students or instructors. The material generally available on elementary crystallography seems to vary between excessively abstruse and involved on the one hand, or too brief on the other. -
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). -
31 May 2013 2013-024 Yeomanite
Title Yeomanite, Pb2O(OH)Cl, a new chain-structured Pb oxychloride from Merehead Quarry, Somerset, England Authors Turner, RW; Siidra, OI; Rumsey, MS; Polekhovsky, YS; Kretser, YL; Krivovichev, SV; Spratt, J; Stanley, Christopher Date Submitted 2016-04-04 2013-024 YEOMANITE CONFIDENTIAL INFORMATION DEADLINE: 31 MAY 2013 2013-024 YEOMANITE Pb2O(OH)Cl Orthorhombic Space group: Pnma a = 6.585(10) b = 3.855(6) c = 17.26(1) Å V = 438(1) Å3 Z = 4 R.W. Turner1*, O.I. Siidra2, M.S. Rumsey3, Y.S. Polekhovsky4, S.V. Krivovichev2, Y.L. Kretser5, C.J. Stanley3, and J. Spratt3 1The Drey, Allington Track, Allington, Salisbury SP4 0DD, Wiltshire, UK 2Department of Crystallography, Geological Faculty, St Petersburg State University, University Embankment 7/9, St Petersburg 199034, Russia 3Department of Earth Sciences, Natural History Museum, Cromwell Road, London SW7 5BD, UK 4Department of Mineral Deposits, St Petersburg State University, University Embankment 7/9, 199034 St Petersburg, Russia 5V.G. Khlopin Radium Institute, Roentgen Street 1, 197101 St Petersburg, Russia *E-mail: [email protected] OCCURRENCE The mineral occurs in the Torr Works (Merehead) Quarry, East Cranmore, Somerset, UK. Yeomanite is associated with mendipite, as a cavity filling in manganese oxide pods. Other oxyhalide minerals that are found hosted in mendipite include diaboleite, chloroxiphite and paralaurionite. Secondary Pb and Cu minerals, including mimetite, wulfenite, cerussite, hydrocerussite, malachite, and crednerite also occur in the same environment. Gangue minerals associated with mineralised manganese pods include aragonite, calcite and barite. Undifferentiated pod-forming Mn oxides are typically a mixture of manganite and pyrolusite, associated with Fe oxyhydroxides such as goethite (Turner, 2006). -
(2016): Formation and Significance of Laurionite in Geothermal Brine
Originally published as: Regenspurg, S., Driba, D. L., Zorn, C. (2016): Formation and significance of laurionite in geothermal brine. ‐ Environmental Earth Sciences, 75, 865 DOI: http://doi.org/10.1007/s12665‐016‐5668‐4 1 Title page: 2 Authors: Simona Regenspurg1*, Dejene Legesse Driba1, Carolin Zorn1 3 Title: Formation and significance of laurionite in geothermal brine 4 Affiliations: 5 1 Helmholtz Centre Potsdam 6 GFZ German Research Centre for Geosciences 7 Section 4.1 Reservoir Technologies 8 International Centre for Geothermal Research (ICGR) 9 Telegrafenberg, D‐14473 Potsdam, Germany 10 11 * corresponding author: email: regens@gfz‐potsdam.de; phone:+49 (0)331 288 1437 12 13 14 15 Abstract 16 The metal lead (Pb) is an environmentally significant, frequently occurring element in 17 geothermal brines. It was found to precipitate from saline fluids predominantly as laurionite 18 (PbOHCl) forming one of the most dominant scaling minerals identified at the geothermal site 19 Groß Schönebeck (Germany). In this study, its formation conditions and relevance for the 20 environment are investigated and discussed. To simulate laurionite precipitation, various 21 amounts of base (NaOH) were added to solutions containing 3 M NaCl, 1 M CaCl2, and 10 mM 22 Pb(NO3)2 at 25 °C, 80 °C, and 133 °C. The formed precipitates were analyzed by X‐ray 23 diffraction and scanning electron microscopy. In nearly all experiments laurionite had formed 24 as the predominant/ only mineral. Experimental results showed the same trends for 25 equilibrium calculations performed with the code PhreeqC and the database “geodat”. The 26 results indicate that the formation of laurionite from geothermal, Pb‐bearing saline brine is 27 very probable, with the pH value as the main controlling parameter for its formation. -
Absolute Dating of Lead Carbonates in Ancient Cosmetics by Radiocarbon
ARTICLE DOI: 10.1038/s42004-018-0034-y OPEN Absolute dating of lead carbonates in ancient cosmetics by radiocarbon Lucile Beck1, Ingrid Caffy1, Emmanuelle Delqué-Količ1, Christophe Moreau1, Jean-Pascal Dumoulin1, Marion Perron1, Hélène Guichard2 & Violaine Jeammet3 1234567890():,; Lead carbonate is one of the major compounds of art and archeology used as an ingredient in paint and cosmetics since Antiquity. Accelerator mass spectrometry radiocarbon dating is usually applied to organic remains. Here we extend radiocarbon dating to lead carbonate, an inorganic material. We demonstrate that lead carbonates can be dated. We also show that natural and manufactured make-up powders can be discriminated by radiocarbon. We find that cerussite used for cosmetics was a natural mineral during the Egyptian Kingdom and then a synthesized compound manufactured by the ancient Greeks. Furthermore, we confirm that phosgenite was artificially produced by the Egyptians about 3500 years ago. Our results confirm the expertize of ancient Egyptians and Greeks in the chemical synthesis of cosmetics. The detection of radiocarbon in lead carbonate holds great promise for art history and provides a new tool for the authentication of paintings by dating the lead white pigment. 1 Laboratoire de Mesure du Carbone 14 (LMC14), LSCE/IPSL, CEA-CNRS-UVSQ, Université Paris-Saclay, 91191 Gif-sur-Yvette, France. 2 Département des Antiquités égyptiennes, Musée du Louvre, Pavillon Mollien, Paris cedex 01 75058, France. 3 Département des Antiquités grecques, étrusques et romaines, Musée du Louvre, Paris Cedex 01 75058, France. Correspondence and requests for materials should be addressed to L.B. (email: [email protected]) COMMUNICATIONS CHEMISTRY | (2018) 1:34 | DOI: 10.1038/s42004-018-0034-y | www.nature.com/commschem 1 ARTICLE COMMUNICATIONS CHEMISTRY | DOI: 10.1038/s42004-018-0034-y he development of the radiocarbon method has had a absolute dating of lead carbonate. -
(New Species) Paralaurionite. ][. LAURIONITE
102 On some lead minerals from Laurium, namely, Laurionite, Phosgenite, Fiedlerite, and (new species) Paralaurionite. By G. F. HERBERT SMITH, B.A., With Chemical Analysis by G. T. PRIOR, IVI.A., F.G.S., Assistants in the Mineral Department of the British Museum. [Read April 5th, 1898.] N this paper are embodied the results of an examination of the speci- I mens of lead slags from Laurium in the British Museum. On some of the specimens a new mineral, paralaurionite, was found, which possesses the same chemical composition as laurionite, but entirely different morphological and optical characters. In addition to crystals of the four minerals given in the title, a few crystals oi matloekite and anglesite were noticed, and on one specimen there is a radiating group of prismatic crystals of penfieldite. ][. LAURIONITE. (a) The morphological characters, Laurionite erystallises in the orthorhombic system. The axial ratios were calculated from the angles between the faces bnl(010:120) and bd(010 : 012), and found to be-- a :b :c----0"7385 : 1:0"83~6 The following values have been previously obtained by Dr. R. KSehlin and Prof. yore Rath-- a : b : c=0"7328 : 1 : 0'8815 K6chlin ~ 0"7178 : 1 : 0"8125 vom Ruth a i Throughout this paper the same letters are used for the faces as in Dana's System of Mineralogy, Sixth Edition. 2 A~,nalen naturhist. Mus. Wien, 1887, ]I. 188, and II. 83 and 127 (Notizen). Dr. KSehlin was the first to describe Laurionite. s Bet. niederrhein. Ges. p. 150, June 6th, 1887. Prof. -
New Mineral Names*
American Mineralogist, Volume 69, pages 810-815, 1984 NEW MINERAL NAMES* Pere J. DuuN. Mrcunel FLerscHEn, Cenl A. FneNcrs, Rrcgnno H. LnNcr-ey, SrepneN A. KlssrN, Jnur,s E. Snrcr-By. Devro A. VnNxo. AND JANETA. Zl-czen Ascharnalmite* 016 . 7.01 H2O. The ideal formula is CaMn?* Si3 016 . 7H2O. Mn valenceassigned the the relation- W. G. Mumme, G. Niedermayr,P. R. Kelly, and W. H. Paar on basisof Gladstone-Dale ship and the red color of the crystals. Bostwickite is readily (1983)Aschamalmite, Pb5.e2Bi2 66Se, from UntersulzbachVal- soluble in | : I HCl. to mineral ley in Salzburg,Austria-"monoclinic heyrovskyite". Neues It does not belong any known Jahrb.Mineral., Monat., 413444. family. Bostwickite crystals are not suitable for single crystal X-ray Microprobeanalysis yielded Pb 62.95,Bi 22.56,and S 14.89, study. The strongestlines (19 given) in the unindexedpowder sum 100.4%,which givesan empiricalformula (on the basisof S patternare: I l. 3(100), 3. 548(30), 2,898(30), 2.567 (40), 2.262(25), : 9) Pb58eBi2.osse. The normalized empirical formula (on the and,2.238(25\.D meas.2.93. basis of S : 8.96 to maintain charge balancefor the given metal Bostwickite was found at Franklin, New Jersey in 1874 as content) is Pb5e2Bi2.66Se. Single-crystal Weissenberg X-ray data divergent sprays of bladed crystals about 250 pm in length. It is from a small prismatic crystal showed it to be monoclinic. sp-ace opticallybiaxial negative,2V : 25", a = 1.775(5), = 1.798(3), " F grotp C2lm,Cm, or C2, with a : 13.71,b = 4.09,c : 3l .434,P y: 1.E00(3);strong dispersion r < y; stronglypleochroic X = f = 91.0",V = 1762.1.3.43.The strongestX-ray lines(32 given) are = red-brown, 7 : yellow-brown; absorption X = Y > Z. -
AFMS Mineral List 2003
American Federation Of Mineralogical Societies AFMS Mineral Classification List New Edition Updated for 2003 AFMS Publications Committee B. Jay Bowman, Chair 1 Internet version of Mineral Classification List. This document may only be downloaded at: http://www.amfed.org/rules/ Introduction to the Mineral Classification List The AFMS Rules Committee voted to eliminate the listing in the Rulebook of references for mineral names except for the AFMS Mineral Classification List. Exhibitors are encouraged to use the AFMS List when exhibiting in the B Division (Minerals). If the mineral they are exhibiting is not on the AFMS List they should note on the Mineral list they present to the judging chairman which reference they did use for the information on their label. The Regional Rules Chairs have been asked to submit names to be added to the list which will be updated with addendum’s each year. In a few years the list should represent most of the minerals generally exhibited out of the 4200+ now recognized by the IMA. This list follows the Glossary of Mineral species which is the IMA approved names for minerals. When the Official name of the mineral includes diacritical mark, they are underlined to indicate they are the IMA approved name. Where usage of old names has been in use for years they have been included, but with the approved spelling underlined following it. The older spelling will be accepted for the present so exhibitors will not have to correct there present label. This list may not contain all mineral species being exhibited. Exhibitors are encouraged to submit names to be added to the list to the Rules committee. -
IMA/CNMNC List of Mineral Names
IMA/CNMNC List of Mineral Name s compiled by Ernest H. Nickel & Monte C. Nichols Supplied through the courtesy of Materials Data, Inc. (http://www.MaterialsData.com) and based on the database MINERAL, which MDI makes available as a free download to the mineralogical community Status* Name CNMNC Approved Formula Strunz Classification Best, Most Recent or Most Complete reference. A Abelsonite NiC£¡H£¢N¤ 10.CA.20 American Mineralogist 63 (1978) 930 A Abenakiite-(Ce) Na¢¦Ce¦(SiO£)¦(PO¤)¦(CO£)¦(SO¢)O 9.CK.10 Canadian Mineralogist 32 (1994), 843 G Abernathyite K(UO¢)AsO¤•3H¢O 8.EB.15 American Mineralogist 41 (1956), 82 A Abhurite (SnÀÈ)¢¡Cl¡¦(OH)¡¤O¦ 3.DA.30 Canadian Mineralogist 23 (1985), 233 D Abkhazite Ca¢Mg¥Si¨O¢¢(OH)¢ 9.DE.10 American Mineralogist 63 (1978), 1023 A Abramovite Pb¢SnInBiS§ 2.HF.25a Zapiski Rossiiskogo Mineralogicheskogo Obshchetstva 136 (2007) (5), 45 D Abrazite K,Ca,Al,Si,O,H¢O 9.GC.05 Canadian Mineralogist 35 (1997), 1571 D Abriachanite Na¢(Fe,Mg)£(FeÁÈ)¢Si¨O¢¢(OH)¢ 9.DE.25 American Mineralogist 63 (1978), 1023 D Absite (U,Ca,Y,Ce)(Ti,Fe)¢O¦ Zapiski Vsesoyuznogo Mineralogicheskogo Obshchestva 92 (1963), 113 A Abswurmbachite CuÀÈ(MnÁÈ)¦O¨(SiO¤) 9.AG.05 Neues Jahrbuch für Mineralogie, Abhandlungen 163 (1991), 117 D Abukumalite (Ca,Ce)¢Y£(SiO¤,PO¤)£(O,OH,F) American Mineralogist 51 (1966), 152 D Acadialite (Ca,K,Na)(Si,Al)£O¦•3H¢O 9.GD.10 Canadian Mineralogist 35 (1997), 1571 G Acanthite Ag¢S 2.BA.30a Handbook of Mineralogy (Anthony et al.), 1 (1990), 1 A Acetamide CH£CONH¢ 10.AA.20 Zapiski Vsesoyuznogo Mineralogicheskogo -
0'7178 : 1 : 0'8125 Vom Raths
102 On some lead minerals from Latl1'ium, namely, Laurionite, Phosgenite, Fiedlerite, and (new species) Paralaurionite. By G. F. HERBJ;;RT SMITH, B.A., With Chemical Analysis by G. T. PRIOR, M.A., F.G.S., Assistants in the Mineral Department of the British Museum. [Read April 5th, 1898.] N this paper are embodied the results of an examination of the speci I mens of leacl slags from Laurium in the British Museum. On some of the specimens a new mineral, paralaurionite, was found, which possesses the same chemICal composi~ion as laurionite, but entirely different morphological and optical characters. In addition to crystals of the four minarals given in the title, a few crystals of matlockite and anglesite were noticed, and on one specimen there is a radiating group of prismatic crystals of penfieldite. 1. LAURIONITE. (a) The morphological cha1·acter.~, Laurionite crystallises in the orthorhombic system. The axial ratios were calculated from the angles between the faces bn1(01O: 120) and bd(OlO : 012), and found to be- a: b: c=0'7385: 1: 0'8346 The following values have been previously obtained by Dr. R. Kochlin and Prof. vom Rath- a: b: c=0'7328: 1 : 0'8315 Kochlin2 0'7178 : 1 : 0'8125 vom RathS 1 Throughout this paper the same letters are used for the faces as in Dana's System oj Miwralof/Y, Sixth Edition. 2 A"nalen natUl'hist. Mus. Wien, 1887, n. 188, and n. 83 and 127 (Notizen). Dr. Kochlin was the first tu describe Laurionite. B Bel'. niederrhein. Ges. p.