Notes on a Recent Discovery Of" Connellite." by W
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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 -
Liroconite Cu2al(Aso4)(OH)4 • 4H2O C 2001-2005 Mineral Data Publishing, Version 1
Liroconite Cu2Al(AsO4)(OH)4 • 4H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. Typically as crystals with a flattened octahedral or lenticular aspect, dominated by {110} and {011} and striated parallel to their intersections, also {001}, {010}, {100}, to 3.6 cm, alone and in sub-parallel groups. May be granular, massive. Physical Properties: Cleavage: On {110}, {011}, indistinct. Fracture: Uneven to conchoidal. Hardness = 2–2.5 D(meas.) = 2.94–3.01 D(calc.) = [3.03] Optical Properties: Transparent to translucent. Color: Sky-blue, bluish green, verdigris-green, emerald-green; pale blue to pale bluish green in transmitted light. Streak: Pale blue to pale green. Luster: Vitreous to resinous. Optical Class: Biaxial (–). Orientation: Y = b; Z ∧ a =25◦. Dispersion: r< v,moderate. α = 1.612(3) β = 1.652(3) γ = 1.675(3) 2V(meas.) = n.d. 2V(calc.) = 72(5)◦ Cell Data: Space Group: I2/a. a = 12.664(2) b = 7.563(2) c = 9.914(3) β =91.32(2)◦ Z=4 X-ray Powder Pattern: Cornwall, England. 6.46 (10), 3.01 (10), 5.95 (9), 2.69 (6), 3.92 (5), 2.79 (5), 2.21 (5) Chemistry: (1) (2) P2O5 3.73 As2O5 23.05 26.54 Al2O3 10.85 11.77 Fe2O3 0.98 CuO 36.38 36.73 H2O 25.01 24.96 Total 100.00 100.00 • (1) Cornwall, England. (2) Cu2Al(AsO4)(OH)4 4H2O. Occurrence: A rare secondary mineral in the oxidized zone of some copper deposits. Association: Olivenite, chalcophyllite, clinoclase, cornwallite, strashimirite, malachite, cuprite, “limonite”. -
B Clifford Frondel
CATALOGUE OF. MINERAL PSEUDOMORPHS IN THE AMERICAN MUSEUM -B CLIFFORD FRONDEL BU.LLETIN OF THEAMRICANMUSEUM' OF NA.TURAL HISTORY. VOLUME LXVII, 1935- -ARTIC-LE IX- NEW YORK Tebruary 26, 1935 4 2 <~~~~~~~~~~~~~7 - A~~~~~~~~~~~~~~~, 4~~~~~~~~~~~~~~~~~~~~~~~~~~~~~4 4 4 A .~~~~~~~~~~~~~~~~~~~~~~~~~~4- -> " -~~~~~~~~~4~~. v-~~~~~~~~~~~~~~~~~~t V-~ ~~~~~~~~~~~~~~~~ 'W. - /7~~~~~~~~~~~~~~~~~~~~~~~~~~7 7-r ~~~~~~~~~-A~~~~ ~ ~ ~ ~ ~ ~ ~ ~ ~ -'c~ ~ ~ ' -7L~ ~ ~ ~ ~ 7 54.9:07 (74.71) Article IX.-CATALOGUE OF MINERAL PSEUDOMORPHS IN THE AMERICAN MUSEUM OF NATURAL HISTORY' BY CLIFFORD FRONDEL CONTENTS PAGE INTRODUCTION .................. 389 Definition.389 Literature.390 New Pseudomorphse .393 METHOD OF DESCRIPTION.393 ORIGIN OF SUBSTITUTION AND INCRUSTATION PSEUDOMORPHS.396 Colloidal Origin: Adsorption and Peptization.396 Conditions Controlling Peptization.401 Volume Relations.403 DESCRIPTION OF SPECIMENS.403 INTRODUCTION DEFINITION.-A pseudomorph is defined as a mineral which has the outward form proper to another species of mineral whose place it has taken through the action of some agency.2 This precise use of the term excludes the regular cavities left by the removal of a crystal from its matrix (molds), since these are voids and not solids,3 and would also exclude those cases in which organic material has been replaced by quartz or some other mineral because the original substance is here not a mineral. The general usage of the term is to include as pseudomorphs both petrifactions and molds, and also: (1) Any mineral change in which the outlines of the original mineral are preserved, whether this surface be a euhedral crystal form or the irregular bounding surface of an embedded grain or of an aggregate. (2) Any mineral change which has been accomplished without change of volume, as evidenced by the undistorted preservation of an original texture or structure, whether this be the equal volume replacement of a single crystal or of a rock mass on a geologic scale. -
Journal of the Russell Society, Vol 4 No 2
JOURNAL OF THE RUSSELL SOCIETY The journal of British Isles topographical mineralogy EDITOR: George Ryba.:k. 42 Bell Road. Sitlingbourn.:. Kent ME 10 4EB. L.K. JOURNAL MANAGER: Rex Cook. '13 Halifax Road . Nelson, Lancashire BB9 OEQ , U.K. EDITORrAL BOARD: F.B. Atkins. Oxford, U. K. R.J. King, Tewkesbury. U.K. R.E. Bevins. Cardiff, U. K. A. Livingstone, Edinburgh, U.K. R.S.W. Brai thwaite. Manchester. U.K. I.R. Plimer, Parkvill.:. Australia T.F. Bridges. Ovington. U.K. R.E. Starkey, Brom,grove, U.K S.c. Chamberlain. Syracuse. U. S.A. R.F. Symes. London, U.K. N.J. Forley. Keyworth. U.K. P.A. Williams. Kingswood. Australia R.A. Howie. Matlock. U.K. B. Young. Newcastle, U.K. Aims and Scope: The lournal publishes articles and reviews by both amateur and profe,sional mineralogists dealing with all a,pecI, of mineralogy. Contributions concerning the topographical mineralogy of the British Isles arc particularly welcome. Not~s for contributors can be found at the back of the Journal. Subscription rates: The Journal is free to members of the Russell Society. Subsc ription rates for two issues tiS. Enquiries should be made to the Journal Manager at the above address. Back copies of the Journal may also be ordered through the Journal Ma nager. Advertising: Details of advertising rates may be obtained from the Journal Manager. Published by The Russell Society. Registered charity No. 803308. Copyright The Russell Society 1993 . ISSN 0263 7839 FRONT COVER: Strontianite, Strontian mines, Highland Region, Scotland. 100 mm x 55 mm. -
Design Rules for Discovering 2D Materials from 3D Crystals
Design Rules for Discovering 2D Materials from 3D Crystals by Eleanor Lyons Brightbill Collaborators: Tyler W. Farnsworth, Adam H. Woomer, Patrick C. O'Brien, Kaci L. Kuntz Senior Honors Thesis Chemistry University of North Carolina at Chapel Hill April 7th, 2016 Approved: ___________________________ Dr Scott Warren, Thesis Advisor Dr Wei You, Reader Dr. Todd Austell, Reader Abstract Two-dimensional (2D) materials are championed as potential components for novel technologies due to the extreme change in properties that often accompanies a transition from the bulk to a quantum-confined state. While the incredible properties of existing 2D materials have been investigated for numerous applications, the current library of stable 2D materials is limited to a relatively small number of material systems, and attempts to identify novel 2D materials have found only a small subset of potential 2D material precursors. Here I present a rigorous, yet simple, set of criteria to identify 3D crystals that may be exfoliated into stable 2D sheets and apply these criteria to a database of naturally occurring layered minerals. These design rules harness two fundamental properties of crystals—Mohs hardness and melting point—to enable a rapid and effective approach to identify candidates for exfoliation. It is shown that, in layered systems, Mohs hardness is a predictor of inter-layer (out-of-plane) bond strength while melting point is a measure of intra-layer (in-plane) bond strength. This concept is demonstrated by using liquid exfoliation to produce novel 2D materials from layered minerals that have a Mohs hardness less than 3, with relative success of exfoliation (such as yield and flake size) dependent on melting point. -
New Mineral Names*
American Mineralogist, Volume 66, pages 1274-1280, 1981 NEW MINERAL NAMES* MICHAEL FLEISCHER AND LOUIS J. CABRI Cyanophillite* ar~ 3.350(50)(110), 3.:208(50)(020), 3.080 (80)(111), 2.781(100) (221,111), 2.750(70)(112), 1.721 (60). Kurt Walenta (1981) Cyanophillite, a new mineral from the Clara ~olor1ess to white, luster vitreous. Cleavages {010}, {OOI}, Mine, near Oberwolfach, Central Black Forest. Chem. der {OIl} good, not easily observed. Hardness about 5. Optically Erde, 40, 195-200 (in German). biaxial positive, ns ex= 1.713, /3 = 1.730, )' = 1.748, 2V +88° (89° Analyses gave CuO 36.3, 32.5; Ah03 8.5, -; Sb203 36.5, 38.3; calc.). Material with Zn:Mg = 1:1 is biaxial, neg., ns. ex= 1.689, H20 19.8; sum 101.1%, corresponding to 10CuO . 2Ah03 . 3Sb2 /3 = 1.707, )' = 1.727, 2V ~ 85°. 03 . 25H20. The mineral is dissolved readily by cold 1:1 HCI, The mineral occurs as coatings and small crystals, largest partly dissolved by 1: 1 HN03. Loss of weight when heated (%) dimension about 1 mm; on prosperite, adamite, and austinite 110° 3.4, 150° 9.5, 200° 19.8%. At 250° the mineral is decomposed from Tsumeb, Namibia. Forms observed {010}, {001}, {Oil}, also and turns black. {IOO}very small. X-ray study shows the mineral to be orthorhombic, space The name is for Robert I. Gait, Curator of Mineralogy, Royal group Pmmb, a = 11.82, b = 10.80, c = 9.64A, Z = 1, D 3.10 Ontario Museum, Toronto. Type material is at the Royal Ontario meas., 3.12 calc. -
Raman Spectroscopic Study of the Mixed Anion Sulphate-Arsenate Mineral Parnauite Cu9[(OH)10|SO4|(Aso4)2].7H2O
QUT Digital Repository: http://eprints.qut.edu.au/ This is the post-print, accepted version of this paper. Published as: Frost, Ray L. and Cejka, Jiri and Keeffe, Eloise C. and Sejkora, Jiri (2009) Raman spectroscopic study of the mixed anion sulphate-arsenate mineral parnauite Cu9[(OH)10|SO4|(AsO4)2].7H2O. Journal of Raman Spectroscopy, 40(11). pp. 1546-1550. © Copyright 2009 John Wiley & Sons, Ltd. Raman spectroscopic study of the mixed anion sulphate-arsenate mineral parnauite . Cu9[(OH)10|SO4|(AsO4)2] 7H2O Ray L. Frost 1 • Jiří Sejkora, 2 Jiří Čejka 1, 2 and Eloise C. Keeffe 1 1 Inorganic Materials Research Program, School of Physical and Chemical Sciences, Queensland University of Technology, GPO Box 2434, Brisbane Queensland 4001, Australia. 2 National Museum, Václavské náměstí 68, CZ-115 79 Praha 1, Czech Republic. The mixed anion mineral parnauite Cu9[(OH)10|SO4|(AsO4)2] 7H2O has been studied by Raman spectroscopy. Characteristic bands associated with arsenate, sulphate, hydroxyl units are identified. Broad bands are observed and are resolved into component bands. Two intense bands at 859 -1 3- and 830 cm are assigned to the ν1 (AsO4) symmetric stretching and ν3 3- (AsO4) antisymmetric stretching modes. The comparatively sharp band at -1 2- 976 cm is assigned to the ν1 (SO4) symmetric stretching mode and a broad -1 2- spectral profile centered upon 1097 cm is attributed to the ν3 (SO4) antisymmetric stretching mode. A comparison of the Raman spectra is made with other arsenate bearing minerals such as carminite, clinotyrolite, kankite, tilasite and pharmacosiderite. KEYWORDS: parnauite, strashimirite, arsenate minerals, Raman spectroscopy, sulphate, hydroxyl, molecular water • Author to whom correspondence should be addressed ([email protected]) 1 INTRODUCTION Parnauite Cu9(AsO4)2(SO4)(OH)10·7H2O is an uncommon mixed anion mineral containing both sulphate and arsenate 1-3 .The mineral is probably orthorhombic with point group 2/m 2/m 2/m 4. -
NO. 7. RESTORMELITE. I Have Obtained on Various Ocasions, from the Restormel Iron Mine, a Mineral Which Might Easilybe Mistaken for One Or Other View Article Online
View Article Online / Journal Homepage / Table of Contents for this issue CHURCH’S CHEMICAL RESEARCHES, ETC. 165 Published on 01 January 1870. Downloaded by University of Lancaster 30/10/2014 18:23:36. XXK- C7iemicaI Researches on hTew or Rare Cornish Minerals. By A. H. CHURCH,M.A., Oxon., Professor of Chemistry, Royal Agricultural College, Cirencester. NO. 7. RESTORMELITE. I have obtained on various ocasions, from the Restormel Iron Mine, a mineral which might easilybe mistaken for one or other View Article Online 166 CHURCH’S CHEMICAL RESEARCHES of the Chinese stones, which are grouped under the vague term agalmatolite. But on comparing the physical and chemical characters of these oriental pinites and pyrophyllites with my Cornish specimeiis, I found such marked differences as to induce me to make a more extended study of the subject. The mate- rial being amorphous, and evidently incompletely altered, was far from promising, but the hope of throwing some light upon the chemical history and formation of similar products, induced me to make several analyses of my specimens. The constancy of their characters and composition was distinctly proved by a physical examination, and by the experimental cheniical results given below. I do not, however, think that I should be in the least degree warranted in assigning specific rank to the Restor- me1 mineral, and though I propose for it the definite name of restorinelite, its proper place appears to me that of a new variety of kaolinite. If we look at the various hydrated aluminium silicates, which have been separately recognized, we shall find that restormelite is near halloysite, but differs from that species by containing 7 per cent. -
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). -
Claringbullite Cu4cl(OH)7 C 2001-2005 Mineral Data Publishing, Version 1
Claringbullite Cu4Cl(OH)7 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Hexagonal. Point Group: 6/m 2/m 2/m. As micaceous or platy crystals, to 1 cm, flattened on {1000}; in groups of divergent plates. Physical Properties: Cleavage: Perfect on {0001}; distinct on {1010} and {1120}. Hardness = Soft. D(meas.) = 3.9 D(calc.) = 3.99 Optical Properties: Transparent to translucent. Color: Blue; pale blue in transmitted light. Luster: Pearly. Optical Class: Uniaxial (–). ω = 1.782 = [1.780] Cell Data: Space Group: P 63/mmc. a = 6.6733(5) c = 9.185(1) Z = 2 X-ray Powder Pattern: Nchanga mine, Zambia or Kambove, Congo. 5.75 (vvs), 2.700 (vvs), 2.445 (vs), 4.89 (s), 4.58 (s), 2.889 (ms), 1.797 (ms) Chemistry: (1) (2) (3) CuO 78.18 74.42 77.85 Cl 8.55 8.30 8.68 H2O [15.14] [19.03] 15.43 SO3 0.06 0.12 −O=Cl2 1.93 1.87 1.96 Total [100.00] [100.00] 100.00 (1) Nchanga mine, Zambia; by electron microprobe, H2O by difference, presence confirmed by elemental analyzer. (2) Kambove, Congo; by electron microprobe, H2O by difference, presence confirmed by elemental analyzer; the mean of five analyses from both localities above corresponds • to Cu8.00(SO4)0.01Cl1.99(OH)14.00 0.68H2O. (3) Cu4Cl(OH)7. Occurrence: In oxidized copper ore or slag, produced under chlorine-rich conditions. Association: Cuprite, malachite, quartz, brochantite, nantokite, paratacamite, connellite, spangolite. Distribution: In the Nchanga mine, Chingola, Zambia. From the M’sesa mine, Kambove, Katanga Province, Congo (Shaba Province, Zaire). -
Preliminary Model of Porphyry Copper Deposits
Preliminary Model of Porphyry Copper Deposits Open-File Report 2008–1321 U.S. Department of the Interior U.S. Geological Survey Preliminary Model of Porphyry Copper Deposits By Byron R. Berger, Robert A. Ayuso, Jeffrey C. Wynn, and Robert R. Seal Open-File Report 2008–1321 U.S. Department of the Interior U.S. Geological Survey U.S. Department of the Interior DIRK KEMPTHORNE, Secretary U.S. Geological Survey Mark D. Myers, Director U.S. Geological Survey, Reston, Virginia: 2008 For product and ordering information: World Wide Web: http://www.usgs.gov/pubprod Telephone: 1-888-ASK-USGS For more information on the USGS—the Federal source for science about the Earth, its natural and living resources, natural hazards, and the environment: World Wide Web: http://www.usgs.gov Telephone: 1-888-ASK-USGS Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government. Although this report is in the public domain, permission must be secured from the individual copyright owners to reproduce any copyrighted materials contained within this report. Suggested citation: Berger, B.R., Ayuso, R.A., Wynn, J.C., and Seal, R.R., 2008, Preliminary model of porphyry copper deposits: U.S. Geological Survey Open-File Report 2008–1321, 55 p. iii Contents Introduction.....................................................................................................................................................1 Regional Environment ...................................................................................................................................3 -
Chalcophyllite from .Chile; by EARL V
E. V. Shannon-Chalcophyllite from Chile. 31 ART. III.-Chalcophyllite from .Chile; by EARL V. SHANNON. The chalcophyllite described in the following article is from the Teniente mine of the Braden Copper Company, east of Rancagua, 0 'Higgins Province, Chile, where the mineral occurred in some abundance in a shear zone 150 meters from the surface. It was associated with ten nantite from which it has presumably been derived by oxidation. The specimens were loaned for investigation Ly Prof. William E. Ford, to whom the writer is indebted for the privilege of describing the mineral. Credit is due Mr. J ames E. Harding, an engineer for the Braden Cop per Company, who collected the material. The alteration of the mineral by dehydration on exposure to the air was noted by Mr. Harding, who packed the material in moist sawdust and sealed it in a tin box, in which it arrived in its original condition in New Haven, where the specimens have for several years since been kept under a bell jar in a moist atmosphere. These are perhaps the only specimens of fresh and unaltered chalcophyllite to be described, or preserved in their unaltered state in any collection. The mineral occurs as emerald-green crusts of closely intergrown tabular crystals averaging about one milli meter in diameter and one-tenth millimeter in thickness. The crusts completely surround irregular fragments of the gangue, which is mainly iron-stained quartz, as though each specimen had formed separately in a clayey matrix; The luster is vitreous-adamantine and the color deep emerald green, there being none of the verdigris green color and pearly luster on the basal pinacoid char acteristically reported for chalcophyllite.