Physical Properties of Salt Anhydrite, and Gypsum
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Halite Nacl C 2001-2005 Mineral Data Publishing, Version 1
Halite NaCl c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Cubic. Point Group: 4/m32/m. Crystals cubic, to 1 m, or octahedral; elongated along [100] or [111], skeletal with hopper-shaped faces. Rarely capillary or stalactitic; granular, compact, massive. Physical Properties: Cleavage: {001}, perfect. Fracture: Conchoidal. Tenacity: Brittle. Hardness = 2–2.5 D(meas.) = 2.168 D(calc.) = 2.165 Soluble in H2O, saline taste; rarely fluoresces red under SW UV. Optical Properties: Transparent. Color: Colorless or white when pure; gray, yellow, orange, pink, red, blue, purple; colorless to faintly tinted in thin section. Streak: White. Luster: Vitreous. Optical Class: Isotropic; weakly anisotropic due to stress. Dispersion: Moderately strong. n = 1.5443 Cell Data: Space Group: Fm3m. a = 5.6404(1) Z = 4 X-ray Powder Pattern: Synthetic. 2.821 (100), 1.994 (55), 1.628 (15), 3.258 (13), 1.261 (11), 1.1515 (7), 1.410 (6) Chemistry: (1) (2) Na 39.00 39.34 K 0.12 Mg 0.03 Ca 0.08 Cl 60.27 60.66 SO4 0.27 Total 99.77 100.00 (1) Cardona, Barcelona, Spain. (2) NaCl. Occurrence: Typically in sedimentary rocks of evaporite association, may form immense beds; also as volcanic sublimates, efflorescences, cave deposits. Crystals are common in multiphase fluid inclusions; may be included in other minerals as a product of intermediate-grade metamorphism. Association: Sylvite, polyhalite, kieserite, carnallite, gypsum, anhydrite, dolomite. Distribution: Of worldwide occurrence. Well-studied deposits include: in Austria, around Hallstadt, Salzburg, and Hall, near Innsbruck, Tirol. From Bex, Vaud, Switzerland. In Germany, from Stassfurt-Leopoldshall, 34 km south of Magdeburg, Saxony-Anhalt. -
Sodium Chloride (Halite, Common Salt Or Table Salt, Rock Salt)
71376, 71386 Sodium chloride (Halite, Common Salt or Table Salt, Rock Salt) CAS number: 7647-14-5 Product Description: Molecular formula: NaCl Appearance: white powder (crystalline) Molecular weight: 58.44 g/mol Density of large crystals: 2.17 g/ml1 Melting Point: 804°C1 Density: 1.186 g/ml (5 M in water)2 2 Solubility: 1 M in H2O, 20°C, complete, clear, colorless 2 pH: 5.0-8.0 (1 M in H2O, 25°C) Store at room temperature Sodium chloride is geologically stable. If kept dry, it will remain a free-flowing solid for years. Traces of magnesium or calcium chloride in commercial sodium chloride adsorb moisture, making it cake. The trace moisture does not harm the material chemically in any way. 71378 BioUltra 71386 BioUltra for molecular biology, 5 M Solution The products are suitable for different applications like purification, precipitation, crystallisation and other applications which require tight control of elemental content. Trace elemental analyses have been performed for all qualities. The molecular biology quality is also tested for absence of nucleases. The Certificate of Analysis provides lot-specific results. Much of the sodium chloride is mined from salts deposited from evaporation of brine of ancient oceans, or recovered from sea water by solar evaporation. Due to the presence of trace hygroscopic minerals, food-grade salt has a small amount of silicate added to prevent caking; as a result, concentrated solutions of "table salt" are usually slightly cloudy in appearance. 71376 and 71386 do not contain any anti-caking agent. Applications: Sodium chloride is a commonly used chemical found in nature and in all body tissue, and is considered an essential nutrient. -
ENVIRONMENTAL RISK ASSESSMENT for GYPSUM TELLS POSITIVE STORY by Karen Bernick
CCPs in Agriculture ENVIRONMENTAL RISK ASSESSMENT FOR GYPSUM TELLS POSITIVE STORY By Karen Bernick mending soils with !ue “…the risk assessment has shown that FGD gypsum gas desulfurization (FGD) contains extremely low concentrations of most trace gypsum o"ers a host of promising bene#ts to elements, about the same as found in mined gypsum agriculture, and this bene#cial use and, in most cases, lower than background soils.” providesA an opportunity for power plants to reduce disposal costs. lead and arsenic trouble spots; and other Chaney says the only risk he has iden- But is it safe? contaminant risks in plant uptake and food. tified occurs if livestock producers He is the lead USDA researcher on the FGD allow ruminants to eat large quanti- $e answer appears to be a resounding gypsum risk assessment. ties of stockpiled gypsum. “If livestock “yes” according to early reports from a producers prevent ruminants from eat- comprehensive risk assessment by the $e USDA-EPA assessment exam- ing gypsum by fencing in stockpiles, U.S. Department of Agriculture (USDA) ines what Chaney calls “new” FGD and limit grazing until after a rainfall to and U.S. Environmental Protection gypsum, a high quality form of syn- wash adhering FGD gypsum from for- Agency (EPA). $e assessment, likely thetic gypsum sought by agricultural age leaves, the sulfate risk is prevented,” to be concluded in 2013, addresses crop producers for its soil improvement he says. potential risks that land applications of bene#ts, calcium and sulfur supplies, FGD gypsum could pose to human health purity and relative low cost versus mined RISK ASSESSMENT or the environment. -
Salt Deposits in the UK
CORE Metadata, citation and similar papers at core.ac.uk Provided by NERC Open Research Archive Halite karst geohazards (natural and man-made) in the United Kingdom ANTHONY H. COOPER British Geological Survey, Keyworth, Nottingham, NG12 5GG, Great Britain COPYRIGHT © BGS/NERC e-mail [email protected] +44 (-0)115 936 3393 +44 (-0)115 936 3475 COOPER, A.H. 2002. Halite karst geohazards (natural and man-made) in the United Kingdom. Environmental Geology, Vol. 42, 505-512. This work is based on a paper presented to the 8th Multidisciplinary Conference on Sinkholes and the Engineering and Environmental impact of karst, Louisville, Kentucky, April 2001. In the United Kingdom Permian and Triassic halite (rock salt) deposits have been affected by natural and artificial dissolution producing karstic landforms and subsidence. Brine springs from the Triassic salt have been exploited since Roman times, or possibly earlier, indicating prolonged natural dissolution. Medieval salt extraction in England is indicated by the of place names ending in “wich” indicating brine spring exploitation at Northwich, Middlewich, Nantwich and Droitwich. Later, Victorian brine extraction in these areas accentuated salt karst development causing severe subsidence problems that remain a legacy. The salt was also mined, but the mines flooded and consequent brine extraction caused the workings to collapse, resulting in catastrophic surface subsidence. Legislation was enacted to pay for the damage and a levy is still charged for salt extraction. Some salt mines are still collapsing and the re-establishment of the post-brine extraction hydrogeological regimes means that salt springs may again flow causing further dissolution and potential collapse. -
Gypsum and Carbon Amendment's
GYPSUM AND CARBON AMENDMENT’S INFLUENCE ON SOIL PROPERTIES, GREENHOUSE GAS EMISSIONS, GROWTH AND NUTRIENT UPTAKE OF RYEGRASS (Lolium perenne) DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Maninder Kaur Walia, M.S. Environment and Natural Resources Graduate Program The Ohio State University 2015 Dissertation Committee: Warren A. Dick, Advisor Rattan Lal Brian K. Slater Frederick C. Michel,Jr. Copyrighted by Maninder Kaur Walia 2015 Abstract Gypsum is a source of calcium and sulfur that improves the physical and chemical properties of the soil. With the benefits associated with gypsum use and the increased availability of synthetic gypsum, its application to soil in Ohio and the Midwest is increasing. Several studies have focused on the effect of gypsum on soil properties. However, little is known about how gypsum affects C stocks in soils. In this study, in addition to gypsum, we also treated the soil with glucose to create a high level of CO2 in the soil profile, and contrasted that with the more slowly released C from plant residues. The overall goal of this dissertation research was to evaluate the effect of plant residues, glucose and gypsum on the growth and nutrient uptake of ryegrass, chemical properties (including total and inorganic C stock) and physical properties of two contrasting soils in Ohio (Wooster silt loam and Hoytville clay loam). Specific objectives of this research were to quantify the effect of (1) gypsum and plant residues on greenhouse gas emissions, (2) gypsum and C amendments on quality of leachate water, (3) gypsum and C amendments addition on C fractions in soils, (4) gypsum, plant residues and glucose addition on soil fertility, growth and nutrients concentrations of ryegrass and (5) gypsum, glucose and plant residues on selected soil physical properties and aggregate-associated C and N. -
“Mining” Water Ice on Mars an Assessment of ISRU Options in Support of Future Human Missions
National Aeronautics and Space Administration “Mining” Water Ice on Mars An Assessment of ISRU Options in Support of Future Human Missions Stephen Hoffman, Alida Andrews, Kevin Watts July 2016 Agenda • Introduction • What kind of water ice are we talking about • Options for accessing the water ice • Drilling Options • “Mining” Options • EMC scenario and requirements • Recommendations and future work Acknowledgement • The authors of this report learned much during the process of researching the technologies and operations associated with drilling into icy deposits and extract water from those deposits. We would like to acknowledge the support and advice provided by the following individuals and their organizations: – Brian Glass, PhD, NASA Ames Research Center – Robert Haehnel, PhD, U.S. Army Corps of Engineers/Cold Regions Research and Engineering Laboratory – Patrick Haggerty, National Science Foundation/Geosciences/Polar Programs – Jennifer Mercer, PhD, National Science Foundation/Geosciences/Polar Programs – Frank Rack, PhD, University of Nebraska-Lincoln – Jason Weale, U.S. Army Corps of Engineers/Cold Regions Research and Engineering Laboratory Mining Water Ice on Mars INTRODUCTION Background • Addendum to M-WIP study, addressing one of the areas not fully covered in this report: accessing and mining water ice if it is present in certain glacier-like forms – The M-WIP report is available at http://mepag.nasa.gov/reports.cfm • The First Landing Site/Exploration Zone Workshop for Human Missions to Mars (October 2015) set the target -
Moving Forwards
Recycling Today Magazine ~> Moving Forward Page 1 of 3 recvdin MoVing Forward By: Timothy G. Townsend May 2003 URL: http:llwww.recyclingtoday,com/arficles/article.asp?lD=4759&CafiD=&SubCatlD= Gypsum drywall is a major component of modern buildings, yet it is often one of the least likely components of debris frem building construction, demolition or renovation to be recycled. Gypsum drywall typically makes up 5 percent to 25 percent of the weight of debris from building-related C&D activities, A typical rule of thumb for drywall generation from construction activities is one pound of drywall per cubic foot of construction. The amount of post-consumer drywall generated in Florida C&D debris in 2000 was estimated at nearly 500,000 tons. Most of this was disposed in unlined landfills. Recovery and recycling is always desired in place of lend- filling when feasible, but several environmentel factors (odor, groundwater contamination) create added incentive for recycling d~JwalL While several gypsum drywall recycling operations exist in North America at the current time, in many areas (Florida for example) drywa!l recycling is relatively nonexistent. This paper describe~ some of the issues facing the C&D debris industry and summarizes the current state of gypsum drywall recycling in North America. DRYWALL BASICS Gypsum drywall, often referred to as gypsum wallbeard or sheet rock, replaced gypsum piaster as the major interior wall surface because of its ease of installation and its fire resistant properties. Gypsum drywal! consists of approximately 90 percent gypsum and 10 percent paper facing and backing. Gypsum is a mineral composed of calcium sulfate (CaSOL and water (H20). -
S40645-019-0306-X.Pdf
Isaji et al. Progress in Earth and Planetary Science (2019) 6:60 Progress in Earth and https://doi.org/10.1186/s40645-019-0306-x Planetary Science RESEARCH ARTICLE Open Access Biomarker records and mineral compositions of the Messinian halite and K–Mg salts from Sicily Yuta Isaji1* , Toshihiro Yoshimura1, Junichiro Kuroda2, Yusuke Tamenori3, Francisco J. Jiménez-Espejo1,4, Stefano Lugli5, Vinicio Manzi6, Marco Roveri6, Hodaka Kawahata2 and Naohiko Ohkouchi1 Abstract The evaporites of the Realmonte salt mine (Sicily, Italy) are important archives recording the most extreme conditions of the Messinian Salinity Crisis (MSC). However, geochemical approach on these evaporitic sequences is scarce and little is known on the response of the biological community to drastically elevating salinity. In the present work, we investigated the depositional environments and the biological community of the shale–anhydrite–halite triplets and the K–Mg salt layer deposited during the peak of the MSC. Both hopanes and steranes are detected in the shale–anhydrite–halite triplets, suggesting the presence of eukaryotes and bacteria throughout their deposition. The K–Mg salt layer is composed of primary halites, diagenetic leonite, and primary and/or secondary kainite, which are interpreted to have precipitated from density-stratified water column with the halite-precipitating brine at the surface and the brine- precipitating K–Mg salts at the bottom. The presence of hopanes and a trace amount of steranes implicates that eukaryotes and bacteria were able to survive in the surface halite-precipitating brine even during the most extreme condition of the MSC. Keywords: Messinian Salinity Crisis, Evaporites, Kainite, μ-XRF, Biomarker Introduction hypersaline condition between 5.60 and 5.55 Ma (Manzi The Messinian Salinity Crisis (MSC) is one of the most et al. -
1469 Vol 43#5 Art 03.Indd
1469 The Canadian Mineralogist Vol. 43, pp. 1469-1487 (2005) BORATE MINERALS OF THE PENOBSQUIS AND MILLSTREAM DEPOSITS, SOUTHERN NEW BRUNSWICK, CANADA JOEL D. GRICE§, ROBERT A. GAULT AND JERRY VAN VELTHUIZEN† Research Division, Canadian Museum of Nature, P.O. Box 3443, Station D, Ottawa, Ontario K1P 6P4, Canada ABSTRACT The borate minerals found in two potash deposits, at Penobsquis and Millstream, Kings County, New Brunswick, are described in detail. These deposits are located in the Moncton Subbasin, which forms the eastern portion of the extensive Maritimes Basin. These marine evaporites consist of an early carbonate unit, followed by a sulfate, and fi nally, a salt unit. The borate assemblages occur in specifi c beds of halite and sylvite that were the last units to form in the evaporite sequence. Species identifi ed from drill-core sections include: boracite, brianroulstonite, chambersite, colemanite, congolite, danburite, hilgardite, howlite, hydroboracite, kurgantaite, penobsquisite, pringleite, ruitenbergite, strontioginorite, szaibélyite, trembathite, veatchite, volkovskite and walkerite. In addition, 41 non-borate species have been identifi ed, including magnesite, monohydrocalcite, sellaite, kieserite and fl uorite. The borate assemblages in the two deposits differ, and in each deposit, they vary stratigraphically. At Millstream, boracite is the most common borate in the sylvite + carnallite beds, with hilgardite in the lower halite strata. At Penobsquis, there is an upper unit of hilgardite + volkovskite + trembathite in halite and a lower unit of hydroboracite + volkov- skite + trembathite–congolite in halite–sylvite. At both deposits, values of the ratio of B isotopes [␦11B] range from 21.5 to 37.8‰ [21 analyses] and are consistent with a seawater source, without any need for a more exotic interpretation. -
Evolution of the Astonishing Naica Giant Crystals in Chihuahua, Mexico
minerals Review Evolution of the Astonishing Naica Giant Crystals in Chihuahua, Mexico Iván Jalil Antón Carreño-Márquez 1 , Isaí Castillo-Sandoval 2, Bernardo Enrique Pérez-Cázares 3, Luis Edmundo Fuentes-Cobas 2 , Hilda Esperanza Esparza-Ponce 2 , Esperanza Menéndez-Méndez 4, María Elena Fuentes-Montero 3 and María Elena Montero-Cabrera 2,* 1 Department of Engineering, Universidad La Salle Chihuahua, Chihuahua 31625, Mexico; [email protected] 2 Department of Environment and Energy, Centro de Investigación en Materiales Avanzados, Chihuahua 31136, Mexico; [email protected] (I.C.-S.); [email protected] (L.E.F.-C.); [email protected] (H.E.E.-P.) 3 Department of Computational Chemistry, Universidad Autónoma de Chihuahua, Chihuahua 31125, Mexico; [email protected] (B.E.P.-C.); [email protected] (M.E.F.-M.) 4 Department Physicochemical Assays, Instituto Eduardo Torroja de Ciencias de la Construcción, 28033 Madrid, Spain; [email protected] * Correspondence: [email protected] Abstract: Calcium sulfate (CaSO4) is one of the most common evaporites found in the earth’s crust. It can be found as four main variations: gypsum (CaSO4·2H2O), bassanite (CaSO4·0.5H2O), soluble Citation: Carreño-Márquez, I.J.A.; anhydrite, and insoluble anhydrite (CaSO4), being the key difference the hydration state of the Castillo-Sandoval, I.; Pérez-Cázares, sulfate mineral. Naica giant crystals’ growth starts from a supersaturated solution in a delicate B.E.; Fuentes-Cobas, L.E.; Esparza- thermodynamic balance close to equilibrium, where gypsum can form nanocrystals able to grow Ponce, H.E.; Menéndez-Méndez, E.; up to 11–12 m long. -
Historical Painting Techniques, Materials, and Studio Practice
Historical Painting Techniques, Materials, and Studio Practice PUBLICATIONS COORDINATION: Dinah Berland EDITING & PRODUCTION COORDINATION: Corinne Lightweaver EDITORIAL CONSULTATION: Jo Hill COVER DESIGN: Jackie Gallagher-Lange PRODUCTION & PRINTING: Allen Press, Inc., Lawrence, Kansas SYMPOSIUM ORGANIZERS: Erma Hermens, Art History Institute of the University of Leiden Marja Peek, Central Research Laboratory for Objects of Art and Science, Amsterdam © 1995 by The J. Paul Getty Trust All rights reserved Printed in the United States of America ISBN 0-89236-322-3 The Getty Conservation Institute is committed to the preservation of cultural heritage worldwide. The Institute seeks to advance scientiRc knowledge and professional practice and to raise public awareness of conservation. Through research, training, documentation, exchange of information, and ReId projects, the Institute addresses issues related to the conservation of museum objects and archival collections, archaeological monuments and sites, and historic bUildings and cities. The Institute is an operating program of the J. Paul Getty Trust. COVER ILLUSTRATION Gherardo Cibo, "Colchico," folio 17r of Herbarium, ca. 1570. Courtesy of the British Library. FRONTISPIECE Detail from Jan Baptiste Collaert, Color Olivi, 1566-1628. After Johannes Stradanus. Courtesy of the Rijksmuseum-Stichting, Amsterdam. Library of Congress Cataloguing-in-Publication Data Historical painting techniques, materials, and studio practice : preprints of a symposium [held at] University of Leiden, the Netherlands, 26-29 June 1995/ edited by Arie Wallert, Erma Hermens, and Marja Peek. p. cm. Includes bibliographical references. ISBN 0-89236-322-3 (pbk.) 1. Painting-Techniques-Congresses. 2. Artists' materials- -Congresses. 3. Polychromy-Congresses. I. Wallert, Arie, 1950- II. Hermens, Erma, 1958- . III. Peek, Marja, 1961- ND1500.H57 1995 751' .09-dc20 95-9805 CIP Second printing 1996 iv Contents vii Foreword viii Preface 1 Leslie A. -
Using Sedimentology to Address the Marine Or Continental Origin of the Permian Hutchinson Salt Member of Kansas
Sedimentology (2019) doi: 10.1111/sed.12665 Using sedimentology to address the marine or continental origin of the Permian Hutchinson Salt Member of Kansas ANNA SOFIA ANDESKIE and KATHLEEN C. BENISON Department of Geology and Geography, West Virginia University, Morgantown, West Virginia, 26506-6300, USA (E-mail: [email protected]) Associate Editor – Hairuo Qing ABSTRACT The Permian Hutchinson Salt Member of the Wellington Formation of the Sumner Group of Kansas (USA) has multiple scientific and industrial uses. Although this member is highly utilized, there has not been a sedimentologi- cal study on these rocks in over 50 years, and no study has investigated the full thickness of this member. Past publications have inferred a marine ori- gin as the depositional environment. Here, this marine interpretation is chal- lenged. The goals of this study are to fully document sedimentological and stratigraphic characteristics of the Permian Hutchinson Salt Member in the Atomic Energy Commission Test Hole 2 core from Rice County, Kansas. This study documents colour, mineralogy, sedimentary textures, sedimentary structures, diagenetic features and stratigraphic contacts in core slab and thin sections. The Hutchinson Salt Member is composed of five lithologies: bedded halite, siliciclastic mudstone, displacive halite, bedded gypsum/ anhydrite and displacive gypsum/anhydrite. These lithologies formed in shallow surface brines and mudflats that underwent periods of flooding, evapoconcentration and desiccation. Of note are the paucity of carbonates, lack of marine-diagnostic fossils, absence of characteristic marine minerals and lithofacies, and the stratigraphic context of the Hutchinson with associ- ated continental deposits. The Hutchinson Salt Member was most likely deposited in an arid continental setting.