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The Journal of Gemmology Data Depository Photomicrographs To
The Journal of Gemmology Data Depository Photomicrographs to accompany the article: Hänni H.A., Brunk R. and Franz L. 2021. An investigation of grinding hardness of some ornamental stones. Journal of Gemmology, 37(6), 2021, 632–643, https://doi.org/10.15506/JoG.2021.37.6.632. The following photomicrographs of thin sections of the samples were made with a Leica DFC490 camera mounted on a Leica DMRD polarising microscope with transmitted light. For each sample, figure A shows the sample in plane-polarised light (II Pol.) and figure B with crossed polarisers (X Pol.); the sample numbers correspond to those in the article. Photomicrographs © L. Franz. 1 1 Aventurine quartz, green: Foliated matrix with aligned quartz (Qz) grains, fuchsite (Fu) tablets and accessory zircon (Zrn). 2 2 Aventurine quartz, orangey red: Mylonitic fabric with quartz (Qz) ribbons and recrystallized grains as well as intergrowths of muscovite with hematite (Ms & Hem). 3 3 Chalcedony, light grey: Intensely interlocked chalcedony (Chc) crystals with random orientation. 4 4 Chrysoprase: In a matrix of tiny chalcedony (Chc) and quartz (Qz) crystals, larger quartz aggregates occur. In microfractures, palisade-shaped chalcedony crystals and quartz grains formed. 5 5 Dumortierite: A banded texture with layers rich in dumortierite (Dum), dumortierite and quartz (Dum & Qz), quartz (Qz) and tourmaline (Tur). 6 6 Granite: The holocrystalline fabric is made up of subhedral plagioclase (Pl), orthoclase (Or), biotite (Bt) and anhedral quartz (Qz). 7 7 Green quartz: A granoblastic texture made up of large quartz (Qz) crystals as well as a microfolded layer of fuchsite (Fu). 8 8 Heliotrope (bloodstone): Green, brown and colourless accumulations of chalcedony (Chc) are recognizable. -
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. -
Wetedge Catalog
PRODUCT CATALOG 1 OUR STORY 3 HOW DID WE FACILITIES 4 GET HERE? PRODUCT LINE Years ago our founder, Laurence Turley, PRIMERA STONE 8 started his career in the mining industry. His worldwide experience in mining led SERENITY STONE 12 him to source exclusive materials from PRISM MATRIX 14 remote regions of the globe. In the early 80’s he focused his energy on the SIGNATURE MATRIX 17 pool industry and later formed Wet Edge Technologies. LUNA QUARTZ 21 Wet Edge Technologies has grown into ALTIMA 25 an industry leader through constant WATER COLOR HUE GUIDE 26 innovation in manufacturing, sourcing and application of our products. We THANK YOU 30 have introduced many new concepts and materials into the pool industry. These new additions enhance both the beauty and durability of our pool finishes. wetedgetechnologies.com 3 THE WET EDGE DIFFERENCE The stones used in our products have been shaped by water over millennia. Their roundness comes from the rushing water of rivers, the ebb and flow WESTERN PRODUCTION DRYING & SCREENING PLANT of tides, the endless motion of ocean waves, the ARIZONA MISSISSIPPI slow march of glacial movement and countless cycles of ice melting. We go to great lengths and expense to discover, recover and import these exotic stones from all over the globe. The roundness of our stones give you the smoothest pool finishes possible. Additionally, we control all aspects of sourcing, sizing and bagging our pebbles to ensure consistency and quality. Our proprietary admixtures used in all Wet Edge products fortify strength and bonding quality of each pool finish, giving you the longest lasting pool finish available. -
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. -
The Rutile Deposits of the Eastern United States
THE RUTILE DEPOSITS OF THE EASTERN UNITED STATES. By THOMAS L. WATSON. INTRODUCTION. The titanium-bearing minerals comprise more than 60 distinct species, grouped under a variety of mineral and chemical forms, chiefly as oxides, titanates, titano-silicates, silicates, columbates, and iantalates. These minerals are widely distributed in a variety of associations and in such quantity as to make titanium a relatively abundant element. Clarke* estimates the. amount of titanium in the solid crust of the earth to be 0.44 per cent, equivalent in oxide to 0.73 per cent, the element thus standing in the ninth place in the scale of abundance, next to potassium. Most of the titanium-bearing minerals, however, are rare and are only of scientific interest. The largest concentrations of the element are as oxide (rutile), as iron titanate (ilmenite), and in iron ferrate (magnetite) as intergrown ilmenite. Of these three forms the prin cipal source of the element at present is rutile. The known workable deposits of rutile, however, are extremely few and widely sepa rated, and as the demand for titanium has greatly increased in the last few years it has been necessary for some uses to turn to ilmenite or highly titaniferous magnetites. This paper briefly summarizes present knowledge of the geology of the rutile deposits in the eastern United States and for the sake of comparison discusses several foreign deposits, each of which has produced some rutile. Of the known deposits in the United, States only those in Virginia are of commercial importance. These have been made the subject of a special report 2 by the Virginia Geological Survey, which was preceded by a preliminary paper on the rutile deposits of Amherst and Nelson counties.3 1 Clarke, F. -
Mineral Collecting Sites in North Carolina by W
.'.' .., Mineral Collecting Sites in North Carolina By W. F. Wilson and B. J. McKenzie RUTILE GUMMITE IN GARNET RUBY CORUNDUM GOLD TORBERNITE GARNET IN MICA ANATASE RUTILE AJTUNITE AND TORBERNITE THULITE AND PYRITE MONAZITE EMERALD CUPRITE SMOKY QUARTZ ZIRCON TORBERNITE ~/ UBRAR'l USE ONLV ,~O NOT REMOVE. fROM LIBRARY N. C. GEOLOGICAL SUHVEY Information Circular 24 Mineral Collecting Sites in North Carolina By W. F. Wilson and B. J. McKenzie Raleigh 1978 Second Printing 1980. Additional copies of this publication may be obtained from: North CarOlina Department of Natural Resources and Community Development Geological Survey Section P. O. Box 27687 ~ Raleigh. N. C. 27611 1823 --~- GEOLOGICAL SURVEY SECTION The Geological Survey Section shall, by law"...make such exami nation, survey, and mapping of the geology, mineralogy, and topo graphy of the state, including their industrial and economic utilization as it may consider necessary." In carrying out its duties under this law, the section promotes the wise conservation and use of mineral resources by industry, commerce, agriculture, and other governmental agencies for the general welfare of the citizens of North Carolina. The Section conducts a number of basic and applied research projects in environmental resource planning, mineral resource explora tion, mineral statistics, and systematic geologic mapping. Services constitute a major portion ofthe Sections's activities and include identi fying rock and mineral samples submitted by the citizens of the state and providing consulting services and specially prepared reports to other agencies that require geological information. The Geological Survey Section publishes results of research in a series of Bulletins, Economic Papers, Information Circulars, Educa tional Series, Geologic Maps, and Special Publications. -
Crystal Structure of Triclinic Lazurite V
Crystallography Reports, Vol. 42, No.6, 1997, pp. 938-945. Translatedfrom Kristallograftya, Vol. 42, No.6, 1997, pp. 1014-1021. Original Russian Text Copyright@ 1997 by Evsyunin, Sapozhnikov, Kashaev, Rastsvetaeva. Crystal Structure of Triclinic Lazurite v. G. Evsyunin*, A. N. Sapozhnikov**, A. A. Kashaev***, and R. K. Rastsvetaeva**** Institute of the Earth's Crust, Siberian Division, Russian Academy of Sciences, * ul. Lermontova 128, Irkutsk, 664033 Russia Vinogradov Institute of Geochemistry and Analytical Chemistry, Siberian Division, ** Russian Academy of Sciences, ul. Favorskogo la, Irkutsk, 664033 Russia Irkutsk Pedagogical Institute, Irkutsk, 664033 Russia *** Shubnikov Institute of Crystallography, Russian Academy of Sciences, **** Leninskii pro 59, Moscow, 117333 Russia Received November 11, 1996 Abstract-The structure of triclinic lazurite from the Malaya-Bystraya deposit (Southern Baikal area) has been determined (sp. gr. PI, Rhkl =0.061,5724 reflections, 210 crystallographically nonequivalent atoms). The form of the incorporation of a sulfur atom into the structure and the character of the displacement and substitution modulations of all the structure atoms have also been determined. INTRODUCTION S04-groups have two orientations that differ by a 90°_ The mineral lazurite has been known in Europe rotation about the fourfold axis. Thus, the form of the since the late 13th century. Since then, it has attracted incorporation of S atoms into the structure and the widespread attention, in particular, as a valuable orna- interpretation of the specific features of this structure mental color stone and as a source of high-quality blue reflected in the presence of superstructural reflections pigment. Being related to the sodalite group, lazurite on the diffraction patterns of lazurite stimulate the fur- has been known for quite a long time as a cubic min- ther structural study of this mineral. -
Stability of the Modulated Structure of Baœkal Lazurite and Its Recrystallization at a Temperature of 600°C Over a Wide Range of Sulfur Dioxide Fugacities V
Crystallography Reports, Vol. 50, Suppl. 1, 2005, pp. S1–S9. Original Russian Text Copyright © 2005 by Tauson, Sapozhnikov. STRUCTURE OF INORGANIC COMPOUNDS Stability of the Modulated Structure of BaÏkal Lazurite and Its Recrystallization at a Temperature of 600°C over a Wide Range of Sulfur Dioxide Fugacities V. L. Tauson and A. N. Sapozhnikov Vinogradov Institute of Geochemistry, Siberian Division, Russian Academy of Sciences, ul. Favorskogo 1a, Irkutsk, 664033 Russia e-mail: [email protected] Received February 8, 2005 Abstract—The stability of three-dimensional incommensurate modulation in cubic lazurite from the BaÏkal region is experimentally investigated at T = 600°C. It is found that the X-ray photoelectron spectra of the annealed samples exhibit a peak corresponding to sulfite and a split peak associated with the (Na,Ca)SO4 sul- fate. It is assumed that the splitting is caused by the ordering of the complexes not involved in the framework. This assumption is confirmed by the presence of a similar split peak in the X-ray photoelectron spectra of tri- clinic lazurite. It is demonstrated that the initial modulation is retained at the fugacity f = 8 × 10–3 bar. The SO2 decisive factors responsible for the retention of the three-dimensional incommensurate modulation are the tem- perature and the fugacity of sulfur dioxide. The latter quantity should be close to the stability boundary of the basic lazurite structure. The growth and transformation mechanisms of the modulation formation are consid- ered. © 2005 Pleiades Publishing, Inc. INTRODUCTION mum concentrations of sulfide sulfur and potassium are typical of the monoclinic modification. -
Download PRIM II Refractive Index Chart
What is Refractive Index (R.I.)? What do the numbers Light travels at different speeds through in the brackets on this chart mean? different types of gemstones due to The numbers in the brackets indicate the Important Note structure of the stone. This affects the tolerance level for readings derived from All testers have been calibrated during the manufacturing process and requires no amount of light refraction and causes the the product. These slight fluctuations further adjustment or user intervention. Self-calibration should not be attempted and is bending of light. The slower the light's indicating a tolerance level are necessary not advised. speed in the material; the greater the due to the optical sensor and electronic REFRACTIVE INDEX CHART FOR bending effect. The refractive index of the components in the product. To minimize any risks associated, users should contact Presidium at gemstone can be defined as the ratio [email protected] or its service center for assistance. PRESIDIUM REFRACTIVE INDEX METER II between the speed of light in vacuum versus the speed of light in gemstone. In the event that users require the manufacturer to re-calibrate the unit, users will have to bear the associated to and fro freight cost for shipping of the unit to the Presidium service center. Presidium Instruments Please note that the gemstone tested on this product must have a flat surface and should Unit 7, 207 Henderson Road Singapore 159550 not be an opaque gemstone. www.presidium.com.sg Family Name of Stones Refractive Index Reading Family -
The Origins of Color in Minerals Four Distinct Physical Theories
American Mineralogist, Volume 63. pages 219-229, 1978 The origins of color in minerals KURT NASSAU Bell Laboratories Murray Hill, New Jersey 07974 Abstract Four formalisms are outlined. Crystal field theory explains the color as well as the fluores- cence in transition-metal-containing minerals such as azurite and ruby. The trap concept, as part of crystal field theory, explains the varying stability of electron and hole color centers with respect to light or heat bleaching, as well as phenomena such as thermoluminescence. The molecular orbital formalism explains the color of charge transfer minerals such as blue sapphire and crocoite involving metals, as well as the nonmetal-involving colors in lazurite, graphite and organically colored minerals. Band theory explains the colors of metallic minerals; the color range black-red-orange- yellow-colorless in minerals such as galena, proustite, greenockite, diamond, as well as the impurity-caused yellow and blue colors in diamond. Lastly, there are the well-known pseudo- chromatic colors explained by physical optics involving dispersion, scattering, interference, and diffraction. Introduction The approach here used is tutorial in nature and references are given for further reading or, in some Four distinct physical theories (formalisms) are instances, for specific examples. Color illustrations of required for complete coverage in the processes by some of the principles involved have been published which intrinsic constituents, impurities, defects, and in an earlier less technical version (Nassau, 1975a). specific structures produce the visual effects we desig- Specific examples are given where the cause of the nate as color. All four are necessary in that each color is reasonably well established, although reinter- provides insights which the others do not when ap- pretations continue to appear even in materials, such plied to specific situations. -
The Seven Crystal Systems
Learning Series: Basic Rockhound Knowledge The Seven Crystal Systems The seven crystal systems are a method of classifying crystals according to their atomic lattice or structure. The atomic lattice is a three dimensional network of atoms that are arranged in a symmetrical pattern. The shape of the lattice determines not only which crystal system the stone belongs to, but all of its physical properties and appearance. In some crystal healing practices the axial symmetry of a crystal is believed to directly influence its metaphysical properties. For example crystals in the Cubic System are believed to be grounding, because the cube is a symbol of the element Earth. There are seven crystal systems or groups, each of which has a distinct atomic lattice. Here we have outlined the basic atomic structure of the seven systems, along with some common examples of each system. Cubic System Also known as the isometric system. All three axes are of equal length and intersect at right angles. Based on a square inner structure. Crystal shapes include: Cube (diamond, fluorite, pyrite) Octahedron (diamond, fluorite, magnetite) Rhombic dodecahedron (garnet, lapis lazuli rarely crystallises) Icosi-tetrahedron (pyrite, sphalerite) Hexacisochedron (pyrite) Common Cubic Crystals: Diamond Fluorite Garnet Spinel Gold Pyrite Silver Tetragonal System Two axes are of equal length and are in the same plane, the main axis is either longer or shorter, and all three intersect at right angles. Based on a rectangular inner structure. Crystal shapes include: Four-sided prisms and pyramids Trapezohedrons Eight-sided and double pyramids Icosi-tetrahedron (pyrite, sphalerite) Hexacisochedron (pyrite) Common Tetragonal Crystals: Anatase Apophyllite Chalcopyrite Rutile Scapolite Scheelite Wulfenite Zircon Hexagonal System Three out of the four axes are in one plane, of the same length, and intersect each other at angles of 60 degrees.