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The Regional Distribution of Zeolites in the Basalts of the Faroe Islands and the Significance of Zeolites As Palaeo- Temperature Indicators
The regional distribution of zeolites in the basalts of the Faroe Islands and the significance of zeolites as palaeo- temperature indicators Ole Jørgensen The first maps of the regional distribution of zeolites in the Palaeogene basalt plateau of the Faroe Islands are presented. The zeolite zones (thomsonite-chabazite, analcite, mesolite, stilbite-heulandite, laumontite) continue below sea level and reach a depth of 2200 m in the Lopra-1/1A well. Below this level, a high temperature zone occurs characterised by prehnite and pumpellyite. The stilbite-heulan- dite zone is the dominant mineral zone on the northern island, Vágar, the analcite and mesolite zones are the dominant ones on the southern islands of Sandoy and Suðuroy and the thomsonite-chabazite zone is dominant on the two northeastern islands of Viðoy and Borðoy. It is estimated that zeolitisa- tion of the basalts took place at temperatures between about 40°C and 230°C. Palaeogeothermal gradients are estimated to have been 66 ± 9°C/km in the lower basalt formation of the Lopra area of Suðuroy, the southernmost island, 63 ± 8°C/km in the middle basalt formation on the northernmost island of Vágar and 56 ± 7°C/km in the upper basalt formation on the central island of Sandoy. A linear extrapolation of the gradient from the Lopra area places the palaeosurface of the basalt plateau near to the top of the lower basalt formation. On Vágar, the palaeosurface was somewhere between 1700 m and 2020 m above the lower formation while the palaeosurface on Sandoy was between 1550 m and 1924 m above the base of the upper formation. -
A Vibrational Spectroscopic Study of the Silicate Mineral Harmotome Â
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 137 (2015) 70–74 Contents lists available at ScienceDirect Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy journal homepage: www.elsevier.com/locate/saa A vibrational spectroscopic study of the silicate mineral harmotome – (Ba,Na,K)1-2(Si,Al)8O16Á6H2O – A natural zeolite ⇑ Ray L. Frost a, , Andrés López a, Lina Wang a,b, Antônio Wilson Romano c, Ricardo Scholz d a School of Chemistry, Physics and Mechanical Engineering, Science and Engineering Faculty, Queensland University of Technology, GPO Box 2434, Brisbane, Queensland 4001, Australia b School of Chemistry and Chemical Engineering, Tianjin University of Technology, No. 391, Bin Shui West Road, Xi Qing District, Tianjin, PR China c Geology Department, Federal University of Minas Gerais, Belo Horizonte, MG 31270-901, Brazil d Geology Department, School of Mines, Federal University of Ouro Preto, Campus Morro do Cruzeiro, Ouro Preto, MG 35400-00, Brazil highlights graphical abstract We have studied the mineral harmotome (Ba,Na,K)1- 2(Si,Al)8O16Á6H2O. It is a natural zeolite. Raman and infrared bands are attributed to siloxane stretching and bending vibrations. A sharp infrared band at 3731 cmÀ1 is assigned to the OH stretching vibration of SiOH units. article info abstract Article history: The mineral harmotome (Ba,Na,K)1-2(Si,Al)8O16Á6H2O is a crystalline sodium calcium silicate which has Received 31 March 2014 the potential to be used in plaster boards and other industrial applications. It is a natural zeolite with cat- Received in revised form 7 July 2014 alytic potential. Raman bands at 1020 and 1102 cmÀ1 are assigned to the SiO stretching vibrations of Accepted 28 July 2014 three dimensional siloxane units. -
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 -
C:\Documents and Settings\Alan Smithee\My Documents\MOTM
I`mt`qx1/00Lhmdq`knesgdLnmsg9Rbnkdbhsd This month’s mineral, scolecite, is an uncommon zeolite from India. Our write-up explains its origin as a secondary mineral in volcanic host rocks, the difficulty of collecting this fragile mineral, the unusual properties of the zeolite-group minerals, and why mineralogists recently revised the system of zeolite classification and nomenclature. OVERVIEW PHYSICAL PROPERTIES Chemistry: Ca(Al2Si3O10)A3H2O Hydrous Calcium Aluminum Silicate (Hydrous Calcium Aluminosilicate), usually containing some potassium and sodium. Class: Silicates Subclass: Tectosilicates Group: Zeolites Crystal System: Monoclinic Crystal Habits: Usually as radiating sprays or clusters of thin, acicular crystals or Hairlike fibers; crystals are often flattened with tetragonal cross sections, lengthwise striations, and slanted terminations; also massive and fibrous. Twinning common. Color: Usually colorless, white, gray; rarely brown, pink, or yellow. Luster: Vitreous to silky Transparency: Transparent to translucent Streak: White Cleavage: Perfect in one direction Fracture: Uneven, brittle Hardness: 5.0-5.5 Specific Gravity: 2.16-2.40 (average 2.25) Figure 1. Scolecite. Luminescence: Often fluoresces yellow or brown in ultraviolet light. Refractive Index: 1.507-1.521 Distinctive Features and Tests: Best field-identification marks are acicular crystal habit; vitreous-to-silky luster; very low density; and association with other zeolite-group minerals, especially the closely- related minerals natrolite [Na2(Al2Si3O10)A2H2O] and mesolite [Na2Ca2(Al6Si9O30)A8H2O]. Laboratory tests are often needed to distinguish scolecite from other zeolite minerals. Dana Classification Number: 77.1.5.5 NAME The name “scolecite,” pronounced SKO-leh-site, is derived from the German Skolezit, which comes from the Greek sklx, meaning “worm,” an allusion to the tendency of its acicular crystals to curl when heated and dehydrated. -
U.S. Department of the Interior U.S. Geological Survey Bibliography on the Occurrence, Properties, and Uses of Zeolites From
U.S. DEPARTMENT OF THE INTERIOR U.S. GEOLOGICAL SURVEY BIBLIOGRAPHY ON THE OCCURRENCE, PROPERTIES, AND USES OF ZEOLITES FROM SEDIMENTARY DEPOSITS, 1985-1992 by Richard A. Sheppard and Evenne W. Sheppard Open-File Report 93-570-A This report is preliminary and has not been reviewed for conformity with U.S. Geological Survey editorial standards (or with the North American Stratigraphic Code). Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government. Denver, Colorado 1993 CONTENTS Page Abstract .............................................................................................. 1 Introduction ......................................................................................... 1 Description of bibliography ....................................................................... 1 Zeolite bibliography ................................................................................ 3 BIBLIOGRAPHY ON THE OCCURRENCE, PROPERTIES, AND USES OF ZEOLITES FROM SEDIMENTARY DEPOSITS, 1985-1992 by Richard A. Sheppard and Evenne W. Sheppard ABSTRACT This bibliography is an alphabetical listing of about 2,000 publications and formal releases, including patents and selected abstracts, from the world literature on the occurrence, properties, and uses of zeolites from sedimentary deposits for the period 1985 to 1992. The bibliography is available as hard copy or on a 3.5-inch floppy diskette, which was prepared on a Macintosh LC computer using EndNote Plus software. Computer -
Apophyllite-(Kf)
December 2013 Mineral of the Month APOPHYLLITE-(KF) Apophyllite-(KF) is a complex mineral with the unusual tendency to “leaf apart” when heated. It is a favorite among collectors because of its extraordinary transparency, bright luster, well- developed crystal habits, and occurrence in composite specimens with various zeolite minerals. OVERVIEW PHYSICAL PROPERTIES Chemistry: KCa4Si8O20(F,OH)·8H20 Basic Hydrous Potassium Calcium Fluorosilicate (Basic Potassium Calcium Silicate Fluoride Hydrate), often containing some sodium and trace amounts of iron and nickel. Class: Silicates Subclass: Phyllosilicates (Sheet Silicates) Group: Apophyllite Crystal System: Tetragonal Crystal Habits: Usually well-formed, cube-like or tabular crystals with rectangular, longitudinally striated prisms, square cross sections, and steep, diamond-shaped, pyramidal termination faces; pseudo-cubic prisms usually have flat terminations with beveled, distinctly triangular corners; also granular, lamellar, and compact. Color: Usually colorless or white; sometimes pale shades of green; occasionally pale shades of yellow, red, blue, or violet. Luster: Vitreous to pearly on crystal faces, pearly on cleavage surfaces with occasional iridescence. Transparency: Transparent to translucent Streak: White Cleavage: Perfect in one direction Fracture: Uneven, brittle. Hardness: 4.5-5.0 Specific Gravity: 2.3-2.4 Luminescence: Often fluoresces pale yellow-green. Refractive Index: 1.535-1.537 Distinctive Features and Tests: Pseudo-cubic crystals with pearly luster on cleavage surfaces; longitudinal striations; and occurrence as a secondary mineral in association with various zeolite minerals. Laboratory analysis is necessary to differentiate apophyllite-(KF) from closely-related apophyllite-(KOH). Can be confused with such zeolite minerals as stilbite-Ca [hydrous calcium sodium potassium aluminum silicate, Ca0.5,K,Na)9(Al9Si27O72)·28H2O], which forms tabular, wheat-sheaf-like, monoclinic crystals. -
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. -
Asbestos Fibers and Other Elongate Mineral Particles: State of the Science and Roadmap for Research
CURRENT INTELLIGENCE BULLETIN 62 Asbestos Fibers and Other Elongate Mineral Particles: State of the Science and Roadmap for Research Revised Edition DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention National Institute for Occupational Safety and Health Cover Photograph: Transitional particle from upstate New York identified by the United States Geological Survey (USGS) as anthophyllite asbestos altering to talc. Photograph courtesy of USGS. CURRENT INTELLIGENCE BULLETIN 62 Asbestos Fibers and Other Elongate Mineral Particles: State of the Science and Roadmap for Research DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention National Institute for Occupational Safety and Health This document is in the public domain and may be freely copied or reprinted. Disclaimer Mention of any company or product does not constitute endorsement by the Na- tional Institute for Occupational Safety and Health (NIOSH). In addition, citations to Web sites external to NIOSH do not constitute NIOSH endorsement of the spon- soring organizations or their programs or products. Furthermore, NIOSH is not responsible for the content of these Web sites. Ordering Information To receive NIOSH documents or other information about occupational safety and health topics, contact NIOSH at Telephone: 1–800–CDC–INFO (1–800–232–4636) TTY: 1–888–232–6348 E-mail: [email protected] or visit the NIOSH Web site at www.cdc.gov/niosh. For a monthly update on news at NIOSH, subscribe to NIOSH eNews by visiting www.cdc.gov/niosh/eNews. DHHS (NIOSH) Publication No. 2011–159 (Revised for clarification; no changes in substance or new science presented) April 2011 Safer • Healthier • PeopleTM ii Foreword Asbestos has been a highly visible issue in public health for over three decades. -
Energetic Characterization of Faujasite Zeolites Using a Sensor Gas Calorimeter
catalysts Article Energetic Characterization of Faujasite Zeolites Using a Sensor Gas Calorimeter Volker Mauer 1,* , Christian Bläker 1, Christoph Pasel 1 and Dieter Bathen 1,2 1 Chair of Thermal Process Engineering, University of Duisburg-Essen, Lotharstraße 1, 47057 Duisburg, Germany; [email protected] (C.B.); [email protected] (C.P.); [email protected] (D.B.) 2 Institute of Energy and Environmental Technology e.V. (IUTA), Bliersheimer Straße 60, 47229 Duisburg, Germany * Correspondence: [email protected]; Tel.: +49-203-3792176 Abstract: In addition to the adsorption mechanism, the heat released during exothermic adsorption influences the chemical reactions that follow during heterogeneous catalysis. Both steps depend on the structure and surface chemistry of the catalyst. An example of a typical catalyst is the faujasite zeolite. For faujasite zeolites, the influence of the Si/Al ratio and the number of Na+ and Ca2+ cations on the heat of adsorption was therefore investigated in a systematic study. A comparison between a NaX (Sodium type X faujasite) and a NaY (Sodium type Y faujasite) zeolite reveals that a higher Si/Al ratio and therefore a smaller number of the cations in faujasite zeolites leads to lower loadings and heats. The exchange of Na+ cations for Ca2+ cations also has an influence on the adsorption process. Loadings and heats first decrease slightly at a low degree of exchange and increase significantly with higher calcium contents. If stronger interactions are required for heterogeneous catalysis, then the CaNaX zeolites must have a degree of exchange above 53%. The energetic contributions show that the highest-quality adsorption sites III and III’ make a contribution to the load-dependent heat of adsorption, which is about 1.4 times (site III) and about 1.8 times (site III’) larger than that of adsorption site II. -
Origin of Analcime in the Neogene Arikli Tuff, Biga Peninsula, NW Turkey
N. Jb. Miner. Abh. 189/1, 21 –34 Article Published online November 2011 Origin of analcime in the Neogene Arikli Tuff, Biga Peninsula, NW Turkey Sevgi Ozen and M. Cemal Goncuoglu With 8 fi gures and 3 tables Abstract: The Arikli Tuff in the Behram Volcanics, NW Anatolia, is characterized by its dominance of authigenic analcime. It was studied by optical microscopy, XRD, SEM/EDX, and ICP for a better understanding of the analcime formation, which occurs as coarse-grained euhedral to subhedral crystals in pores and pumice fragments as well as in clusters or fi ne-grained single crystals embedded in the matrix. Besides analcime, K-feldspar, dolomite, and smectite are found as further authigenic minerals. Based on the dominance of these authigenic minerals, the tuffs are petrographically separated into phyllosilicate-bearing vitric tuff, dolomite- rich vitric tuff, and K-feldspar-dominated vitric tuff. No precursor of zeolites other than analcime was detected. Petrographical and SEM investigations indicate that euhedral to subhedral analcime crystals found as a coarse-grained fi lling cement in voids and pumice fragments are precipitated from pore water, whereas fi ne-grained disseminated crystals are formed by the dissolution- precipitation of glassy material. Hydrolysis of glassy material that is similar in composition to analcime provides the additional Na, Al, Si, and K elements which are necessary for the formation of analcime. Key words: Alteration, analcime, Neogene tuff, NW Turkey, volcanic glass. Introduction (Kopenez), Kirka (Karaoren), Urla, Bahcecik-Golpazari- Goynuk, Nallihan-Cayirhan-Beypazari-Mihaliccik, Ka- Tuffs deposited in lacustrine conditions present a unique lecik-Hasayaz-Sabanozu-Candir, Polatli-Mülk-Oglakci- opportunity to study the zeolite-forming processes. -
Mineral Reactions in the Sedimentary Deposits of the Lake Magadi Region, Kenya
Mineral reactions in the sedimentary deposits of the Lake Magadi region, Kenya RONALD C. SURD AM Department of Geology, University of Wyoming, Laramie, Wyoming 82071 HANS P. EUGSTER Department of Earth and Planetary Science, Johns Hopkins University, Baltimore, Maryland 21218 ABSTRACT hand, the initial alkalic zeolite that will form in a specific alkaline lake environment cannot yet be predicted with confidence. Among The authigenic minerals, principally zeolites, in the Pleistocene to the many parameters controlling zeolite distribution, the compo- Holocene consolidated and unconsolidated sediments of the sitions of the volcanic glasses and of the alkaline solutions are cer- Magadi basin in the Eastern Rift Valley of Kenya have been inves- tainly of primary importance. tigated. Samples were available from outcrops as well as drill cores. Most zeolite studies are concerned with fossil alkaline lakes. The following reactions can be documented: (1) trachytic glass + While it is generally easy to establish the composition of the vol- H20 —» erionite, (2) trachytic glass + Na-rich brine —* Na-Al-Si gel, canic glass, the brines responsible for the authigenic reactions have + + (3) erionite + Na analcime + K + Si02 + H20, (4) Na-Al-Si long since disappeared. To overcome this handicap, it is desirable gelanalcime + H20, (5) calcite + F-rich brine—> fluorite + C03 , to investigate an alkaline lake environment for which glass as well (6) calcite + Na-rich brine —» gaylussite, and (7) magadiite —• as brine compositions can be determined — in other words, a + quartz + Na + H20. Erionite is the most common zeolite present, modern alkaline lake environment. Such an environment is Lake but minor amounts of chabazite, clinoptilolite, mordenite, and Magadi of Kenya. -
Hydrogen-Bonded Water in Laumontite I: X-Ray Powder Diffraction Study Of
American Mineralogist, Volume 88, pages 277–287, 2003 Hydrogen-bonded water in laumontite I: X-ray powder diffraction study of water site occupancy and structural changes in laumontite during room-temperature isothermal hydration/dehydration THRÁINN FRIDRIKSSON,1,* DAVID L. BISH,2 AND DENNIS K. BIRD1 1Department of Geological and Environmental Sciences, Stanford University, Stanford, California 94305-2115, U.S.A. 2Hydrology, Geochemistry, and Geology, MS D469, Los Alamos National Laboratory, Los Alamos, New Mexico 87545, U.S.A. ABSTRACT The response of the laumontite crystal structure to hydration/dehydration was evaluated using Rietveld refinements with XRD data collected under controlled PH2O conditions at ~28.5 ∞C. Refined water contents per unit cell (unit-cell formula: Ca4Al8Si16O48·nH2O) ranged between 12.5 H2O at 0.11 mbar PH2O and 17.3 H2O at 37.6 mbar. The occupancy of the two water sites hosting hydrogen- bonded water molecules, W5 and W1, ranged from 13% to 100% and from 2% to 86%, respectively. During hydration of W5, between 0.11 and 5 mbar, the unit cell expanded continuously and revers- ibly from 1327 to 1348 Å3. The unit-cell volume remained nearly constant between 5 and 28 mbar. The hydration/dehydration of W1 exhibited hysteresis; hydration occurred at ~29 mbar and dehy- dration at ~24 mbar. During hydration of W1 at ~29 mbar the unit cell expanded from 1351 to 1384 Å3. Further hydration of W1 above 29 mbar resulted in gradual and reversible unit-cell expansion to 1386 Å3 at 37.6 mbar. Hydration/dehydration of W5 is a continuous reaction typical for zeolites.