Lab 3: Silicate Minerals
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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. -
Bedrock Geology Glossary from the Roadside Geology of Minnesota, Richard W
Minnesota Bedrock Geology Glossary From the Roadside Geology of Minnesota, Richard W. Ojakangas Sedimentary Rock Types in Minnesota Rocks that formed from the consolidation of loose sediment Conglomerate: A coarse-grained sedimentary rock composed of pebbles, cobbles, or boul- ders set in a fine-grained matrix of silt and sand. Dolostone: A sedimentary rock composed of the mineral dolomite, a calcium magnesium car- bonate. Graywacke: A sedimentary rock made primarily of mud and sand, often deposited by turbidi- ty currents. Iron-formation: A thinly bedded sedimentary rock containing more than 15 percent iron. Limestone: A sedimentary rock composed of calcium carbonate. Mudstone: A sedimentary rock composed of mud. Sandstone: A sedimentary rock made primarily of sand. Shale: A deposit of clay, silt, or mud solidified into more or less a solid rock. Siltstone: A sedimentary rock made primarily of sand. Igneous and Volcanic Rock Types in Minnesota Rocks that solidified from cooling of molten magma Basalt: A black or dark grey volcanic rock that consists mainly of microscopic crystals of pla- gioclase feldspar, pyroxene, and perhaps olivine. Diorite: A plutonic igneous rock intermediate in composition between granite and gabbro. Gabbro: A dark igneous rock consisting mainly of plagioclase and pyroxene in crystals large enough to see with a simple magnifier. Gabbro has the same composition as basalt but contains much larger mineral grains because it cooled at depth over a longer period of time. Granite: An igneous rock composed mostly of orthoclase feldspar and quartz in grains large enough to see without using a magnifier. Most granites also contain mica and amphibole Rhyolite: A felsic (light-colored) volcanic rock, the extrusive equivalent of granite. -
Crystallization History of Gabbroic Shergottite Nwa 6963 As Revealed by Pyroxene Zoning
Lunar and Planetary Science XLVIII (2017) 1504.pdf CRYSTALLIZATION HISTORY OF GABBROIC SHERGOTTITE NWA 6963 AS REVEALED BY PYROXENE ZONING. A. L. Meado1, S. P. Schwenzer2, S. J. Hammond2, and J. Filiberto1,2, 1Southern Illinois University, Department of Geology, Carbondale IL 62901, USA. [email protected], 2School of Enviroment, Earth, and Ecosystem Sciences, The Open University, Walton Hall, Milton Keynes, MK7 6AA, UK. Introduction: NorthWest Africa (NWA) 6963 is an comprised of 40 to 120 measured points depending on intriguing new coarse grained Martian meteorite that grain size. This method produced precise zoing profiles further extends our sample collection both composition- used to interpret NWA 6963 petrogenetic history. Meas- ally and texturally [1]. It was originally documented as urements too close to the edge of grains, melt inclusions, a basaltic shergottite because the pyroxene composi- sulfides, fractures, or alteration were removed from zon- tions [2, 3] and modal abundances are similar to Sher- ing profiles. Outliers were identified by obvious gotty. However, recent work reclassified NWA 6963 as changes in bulk chemisty, poor oxide weight totals, and an intrusive, gabbroic Martian meteorite because of the visual inspection of back scatter electron (BSE) images. large oriented pyroxene crystals [1]. This investigation Element maps of three pyroxene grains were produced will focus on NWA 6963 pyroxene zoning profiles and to better interpret zoning profiles. interpreting igneous processes related to its crystalliza- Trace elements have recently been analyzed by laser tion history. ablation-ICPMS at the Open University, UK. The data Compositional zoning of pyroxene crystals in basal- is currently being reduced to further interpret pyroxene tic shergottites have previously been interpreted for pe- zoning profiles in NWA 6963. -
Carbonation and Decarbonation Reactions: Implications for Planetary Habitability K
American Mineralogist, Volume 104, pages 1369–1380, 2019 Carbonation and decarbonation reactions: Implications for planetary habitability k E.M. STEWART1,*,†, JAY J. AGUE1, JOHN M. FERRY2, CRAIG M. SCHIFFRIES3, REN-BIAO TAO4, TERRY T. ISSON1,5, AND NOAH J. PLANAVSKY1 1Department of Geology & Geophysics, Yale University, P.O. Box 208109, New Haven, Connecticut 06520-8109, U.S.A. 2Department of Earth and Planetary Sciences, Johns Hopkins University, 3400 N. Charles Street, Baltimore, Maryland 21218, U.S.A. 3Geophysical Laboratory, Carnegie Institution for Science, 5251 Broad Branch Road NW, Washington, D.C. 20015, U.S.A. 4School of Earth and Space Sciences, MOE Key Laboratory of Orogenic Belt and Crustal Evolution, Peking University, Beijing 100871, China 5School of Science, University of Waikato, 101-121 Durham Street, Tauranga 3110, New Zealand ABSTRACT The geologic carbon cycle plays a fundamental role in controlling Earth’s climate and habitability. For billions of years, stabilizing feedbacks inherent in the cycle have maintained a surface environ- ment that could sustain life. Carbonation/decarbonation reactions are the primary mechanisms for transferring carbon between the solid Earth and the ocean–atmosphere system. These processes can be broadly represented by the reaction: CaSiO3 (wollastonite) + CO2 (gas) ↔ CaCO3 (calcite) + SiO2 (quartz). This class of reactions is therefore critical to Earth’s past and future habitability. Here, we summarize their significance as part of the Deep Carbon Obsevatory’s “Earth in Five Reactions” project. In the forward direction, carbonation reactions like the one above describe silicate weathering and carbonate formation on Earth’s surface. Recent work aims to resolve the balance between silicate weathering in terrestrial and marine settings both in the modern Earth system and through Earth’s history. -
Module 7 Igneous Rocks IGNEOUS ROCKS
Module 7 Igneous Rocks IGNEOUS ROCKS ▪ Igneous Rocks form by crystallization of molten rock material IGNEOUS ROCKS ▪ Igneous Rocks form by crystallization of molten rock material ▪ Molten rock material below Earth’s surface is called magma ▪ Molten rock material erupted above Earth’s surface is called lava ▪ The name changes because the composition of the molten material changes as it is erupted due to escape of volatile gases Rocks Cycle Consolidation Crystallization Rock Forming Minerals 1200ºC Olivine High Ca-rich Pyroxene Ca-Na-rich Amphibole Intermediate Na-Ca-rich Continuous branch Continuous Discontinuous branch Discontinuous Biotite Na-rich Plagioclase feldspar of liquid increases liquid of 2 Temperature decreases Temperature SiO Low K-feldspar Muscovite Quartz 700ºC BOWEN’S REACTION SERIES Rock Forming Minerals Olivine Ca-rich Pyroxene Ca-Na-rich Amphibole Na-Ca-rich Continuous branch Continuous Discontinuous branch Discontinuous Biotite Na-rich Plagioclase feldspar K-feldspar Muscovite Quartz BOWEN’S REACTION SERIES Rock Forming Minerals High Temperature Mineral Suite Olivine • Isolated Tetrahedra Structure • Iron, magnesium, silicon, oxygen • Bowen’s Discontinuous Series Augite • Single Chain Structure (Pyroxene) • Iron, magnesium, calcium, silicon, aluminium, oxygen • Bowen’s Discontinuos Series Calcium Feldspar • Framework Silicate Structure (Plagioclase) • Calcium, silicon, aluminium, oxygen • Bowen’s Continuous Series Rock Forming Minerals Intermediate Temperature Mineral Suite Hornblende • Double Chain Structure (Amphibole) -
Carbonation and Decarbonation Reactions: Implications for Planetary Habitability K
American Mineralogist, Volume 104, pages 1369–1380, 2019 Carbonation and decarbonation reactions: Implications for planetary habitability k E.M. STEWART1,*,†, JAY J. AGUE1, JOHN M. FERRY2, CRAIG M. SCHIFFRIES3, REN-BIAO TAO4, TERRY T. ISSON1,5, AND NOAH J. PLANAVSKY1 1Department of Geology & Geophysics, Yale University, P.O. Box 208109, New Haven, Connecticut 06520-8109, U.S.A. 2Department of Earth and Planetary Sciences, Johns Hopkins University, 3400 N. Charles Street, Baltimore, Maryland 21218, U.S.A. 3Geophysical Laboratory, Carnegie Institution for Science, 5251 Broad Branch Road NW, Washington, D.C. 20015, U.S.A. 4School of Earth and Space Sciences, MOE Key Laboratory of Orogenic Belt and Crustal Evolution, Peking University, Beijing 100871, China 5School of Science, University of Waikato, 101-121 Durham Street, Tauranga 3110, New Zealand ABSTRACT The geologic carbon cycle plays a fundamental role in controlling Earth’s climate and habitability. For billions of years, stabilizing feedbacks inherent in the cycle have maintained a surface environ- ment that could sustain life. Carbonation/decarbonation reactions are the primary mechanisms for transferring carbon between the solid Earth and the ocean–atmosphere system. These processes can be broadly represented by the reaction: CaSiO3 (wollastonite) + CO2 (gas) ↔ CaCO3 (calcite) + SiO2 (quartz). This class of reactions is therefore critical to Earth’s past and future habitability. Here, we summarize their signifcance as part of the Deep Carbon Obsevatory’s “Earth in Five Reactions” project. In the forward direction, carbonation reactions like the one above describe silicate weathering and carbonate formation on Earth’s surface. Recent work aims to resolve the balance between silicate weathering in terrestrial and marine settings both in the modern Earth system and through Earth’s history. -
Nature of Interlayer Material in Silicate Clays of Selected Oregon Soils
AN ABSTRACT OF THE THESIS OF PAUL C, SINGLETON for the Ph.D. in Soils (Name) (Degree) (Major) Date thesis is presented July 28, 1965 Title NATURE OF INTERLAYER MATERIAL IN SILICATE CLAYS OF SELECTED OREGON SOILS - Redacted for Privacy Abstract approved = ajor professor) Ç A study was conducted to investigate the nature of hydroxy interlayers in the chlorite -like intergrade clays of three Oregon soils with respect to kind, amount, stability, and conditions of formation. The clays of the Hembre, Wren, and Lookout soils, selected to represent weathering products originating from basaltic materials under humid, subhumid, and semi -arid climatic conditions respectively, were subjected to a series of progressive treatments designed to effect a differential dissolution of the materials intimately asso- ciated with them. The treatments, chosen to represent a range of increasing severity of dissolution, were (1) distilled water plus mechanical stirring, (2) boiling 2% sodium carbonate, (3) buffered sodium citrate -dithionite, (4) boiling sodium hydroxide, and (5) preheating to 400 °C for 4 hours plus boiling sodium hydroxide. Extracts from the various steps of the dissolution procedure were chemically analyzed in order to identify the materials removed from the clays. X -ray diffraction analysis and cation exchange capacity determinations were made on the clays after each step, and any differences noted in the measured values were attributed to the removal of hydroxy interlayers from the clays. Hydroxy interlayers were found to occur more in the Hembre and Wren soils than in the Lookout soil, with the most stable interlayers occurring in the Wren. Soil reaction was one of the major differences between these soils. -
Lab 2: Silicate Minerals
GEOLOGY 640: Geology through Global Arts and Artifacts LAB 2: SILICATE MINERALS FRAMEWORK SILICATES The framework silicates quartz and feldspar are the most common minerals in Earth’s crust. Quartz (SiO 2) is one of the few common minerals that is harder than a streak plate. It may display numerous colors (purple= amethyst ; pink= rose quartz ; brown= smoky quartz ; yellow-orange= citrine ). It may form long hexagonal crystals but lacks cleavage, and instead breaks along irregular, curving surfaces (conchoidal fracture). In many cases quartz forms masses of microscopic crystals (e.g., chert, flint, chalcedony ) that still maintain the hardness and conchoidal fracture of quartz. Banded chalcedony is called agate , whereas reddish chalcedony is called carnelian (bloodstone). Plagioclase is a group of feldspar minerals that have complete solid solution from NaAlSi 3O8 ( albite ) to CaAl 2Si 2O8 ( anorthite ). Na-rich plagioclase tends to white in hands sample, whereas Ca-rich plagioclase tends to be dark grey. Twinning is the intergrowth of two or more crystals in a symmetrical fashion by the sharing of lattice points in adjacent crystals. In plagioclase, the most common twins are planar and repeated (polysynthetic twinning), resulting in the striations that are characteristic of plagioclase in hand-sample. Twinning tends to be better developed in Ca-plagioclase minerals. Ca-rich plagioclase (labradorite and anorthite) may also display iridescent colors (mostly blue). Iridescent albite is rare and is known as the semi-precious gem moonstone . Microcline (KAlSi 3O8) is the most common alkali feldspar. It is similar to plagioclase in most of its optical properties (hard, blocky, 2 cleavages at 90°). -
Plagioclase Peridotite Or Olivine- Plagioclase Assemblage In
Plagioclase peridotite or olivine- plagioclase assemblage in orogenic peridotites: its implications on high-temperature decompression of the subcontinental lithosphere- asthenosphere boundary zone K. Ozawa, Univ. Tokyo; C. J. Garrido, Univ. Granada; K. Hidas, Univ. Granada; J-L. Bodinier, Geosciences Montpellier; T. Aoki, Univ. Tokkyo; F. Boudier, Univ. Montpellier EGU, Vienna, 6 May, 2020 1 What we did in this study. • We have examined four orogenic peridotite complexes, Ronda, Pyrenees, Lanzo, and Horoman, to clarify the extent of shallow thermal processing based on olivine-plagioclase assemblage in plagioclase lherzolite. • The key approach of this study is to look at textural relationships between olivine and plagioclase, whose scale and mode of occurrence provide extent and strength of thermal processing in the shallow upper mantle and thus asthenosphere activity related to the exhumation of lithospheric mantle. 2 Plagioclase lherzolite proxy for dynamics of LAB • Plagioclase (pl) -olivine (ol) assemblage in fertile system is not stable even at the depth of the upper most subcontinental lithospheric mantle (SCLM ) because ….. (1) The common crustal thickness in normal non-cratonic SCLM is ~35km. (2) The Moho temperature for the mean steady-state continental geotherm is much lower than 600°C. (3) The upper stability limit of plagioclase (plagioclase to spinel facies transition) becomes shallower with decrease in temperature. (4) Kinetic barrier for subsolidus reactions in the peridotite system becomes enormous at temperatures below -
Sr–Pb Isotopes Signature of Lascar Volcano (Chile): Insight Into Contamination of Arc Magmas Ascending Through a Thick Continental Crust N
Sr–Pb isotopes signature of Lascar volcano (Chile): Insight into contamination of arc magmas ascending through a thick continental crust N. Sainlot, I. Vlastélic, F. Nauret, S. Moune, F. Aguilera To cite this version: N. Sainlot, I. Vlastélic, F. Nauret, S. Moune, F. Aguilera. Sr–Pb isotopes signature of Lascar volcano (Chile): Insight into contamination of arc magmas ascending through a thick continental crust. Journal of South American Earth Sciences, Elsevier, 2020, 101, pp.102599. 10.1016/j.jsames.2020.102599. hal-03004128 HAL Id: hal-03004128 https://hal.uca.fr/hal-03004128 Submitted on 13 Nov 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. Copyright Manuscript File Sr-Pb isotopes signature of Lascar volcano (Chile): Insight into contamination of arc magmas ascending through a thick continental crust 1N. Sainlot, 1I. Vlastélic, 1F. Nauret, 1,2 S. Moune, 3,4,5 F. Aguilera 1 Université Clermont Auvergne, CNRS, IRD, OPGC, Laboratoire Magmas et Volcans, F-63000 Clermont-Ferrand, France 2 Observatoire volcanologique et sismologique de la Guadeloupe, Institut de Physique du Globe, Sorbonne Paris-Cité, CNRS UMR 7154, Université Paris Diderot, Paris, France 3 Núcleo de Investigación en Riesgo Volcánico - Ckelar Volcanes, Universidad Católica del Norte, Avenida Angamos 0610, Antofagasta, Chile 4 Departamento de Ciencias Geológicas, Universidad Católica del Norte, Avenida Angamos 0610, Antofagasta, Chile 5 Centro de Investigación para la Gestión Integrada del Riesgo de Desastres (CIGIDEN), Av. -
Sieve-Textured Plagioclase in Volcanic Rocks Produced by Rapid
American Mineralogist, Volume 77, pages 1242-1249, 1992 Sieve-texturedplagioclase in volcanic rocks producedby rapid decompression SrnpHnN T. NBr,soN, Anr MoNrANrA.* Department of Earth and SpaceSciences, UCLA, Los Angeles,California 90024-1567,U.S.A. Ansrnlcr Disequilibrium textures,particularly the coarsesieve texture ofplagioclase,are common in orogenic volcanic rocks. The textures are usually interpreted as resulting from magma mixing, but they may occur by rapid decompression,where heat loss is minor relative to the ascent rate. We conducted high-pressurepiston-cylinder experiments on an andesite to test this hypothesis. Experiments starting at 12 kbar, followed by isothermal pressure releasein increments of 2, 4, and 6 kbar, produce sieve textures in plagioclasevery much like those in many volcanic rocks. Therefore, the presenceof sieve-texturedplagioclase should not be taken as a priori evidencefor magma mixing. Many volcanic systemsprob- ably experienceconditions of decompressionsimilar to those simulated in this study, and decompressionis considered to be a simple mechanism to produce such textures, as it requires no addition of heat or mass. Rapid decompressionmay also operate in conjunc- tion with magmamixing. INrnonucrroN One interpretation of coarse sieve textures similar to Plagioclasecommonly exhibits a variety of disequilib- those in Figure I is rapid skeletal growth resulting from rium textures in volcanic rocks, especially in orogenic undercooling(Kuo and Kirkpatrick, 1982).However, melt andesites.These textures often -
An Investigation Into the UV Fluorescence of Feldspar Group
An Investigation into UV Fluorescence in Feldspar Group Minerals Natasha Morrison Submitted in Partial Fulfillment of the Requirement for the Degree of Honours Bachelor of Science, Department of Earth Sciences At Dalhousie University Halifax, Nova Scotia March 17th, 2013 Submitted to: Dr. Richard Cox Dr. Martin Gibling 1 Distribution License DalSpace requires agreement to this non-exclusive distribution license before your item can appear on DalSpace. NON-EXCLUSIVE DISTRIBUTION LICENSE You (the author(s) or copyright owner) grant to Dalhousie University the non-exclusive right to reproduce and distribute your submission worldwide in any medium. You agree that Dalhousie University may, without changing the content, reformat the submission for the purpose of preservation. You also agree that Dalhousie University may keep more than one copy of this submission for purposes of security, back-up and preservation. You agree that the submission is your original work, and that you have the right to grant the rights contained in this license. You also agree that your submission does not, to the best of your knowledge, infringe upon anyone's copyright. If the submission contains material for which you do not hold copyright, you agree that you have obtained the unrestricted permission of the copyright owner to grant Dalhousie University the rights required by this license, and that such third-party owned material is clearly identified and acknowledged within the text or content of the submission. If the submission is based upon work that has been sponsored or supported by an agency or organization other than Dalhousie University, you assert that you have fulfilled any right of review or other obligations required by such contract or agreement.