Brucite – Industrial Mineral with a Future George J
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
The Forsterite-Anorthite-Albite System at 5 Kb Pressure Kristen Rahilly
The Forsterite-Anorthite-Albite System at 5 kb Pressure Kristen Rahilly Submitted to the Department of Geosciences of Smith College in partial fulfillment of the requirements for the degree of Bachelor of Arts John B. Brady, Honors Project Advisor Acknowledgements First I would like to thank my advisor John Brady, who patiently taught me all of the experimental techniques for this project. His dedication to advising me through this thesis and throughout my years at Smith has made me strive to be a better geologist. I would like to thank Tony Morse at the University of Massachusetts at Amherst for providing all of the feldspar samples and for his advice on this project. Thank you also to Michael Jercinovic over at UMass for his help with last-minute carbon coating. This project had a number of facets and I got assistance from many different departments at Smith. A big thank you to Greg Young and Dale Renfrow in the Center for Design and Fabrication for patiently helping me prepare and repair the materials needed for experiments. I’m also grateful to Dick Briggs and Judith Wopereis in the Biology Department for all of their help with the SEM and carbon coater. Also, the Engineering Department kindly lent their copy of LabView software for this project. I appreciated the advice from Mike Vollinger within the Geosciences Department as well as his dedication to driving my last three samples over to UMass to be carbon coated. The Smith Tomlinson Fund provided financial support. Finally, I need to thank my family for their support and encouragement as well as my friends here at Smith for keeping this year fun and for keeping me balanced. -
Mineral Processing
Mineral Processing Foundations of theory and practice of minerallurgy 1st English edition JAN DRZYMALA, C. Eng., Ph.D., D.Sc. Member of the Polish Mineral Processing Society Wroclaw University of Technology 2007 Translation: J. Drzymala, A. Swatek Reviewer: A. Luszczkiewicz Published as supplied by the author ©Copyright by Jan Drzymala, Wroclaw 2007 Computer typesetting: Danuta Szyszka Cover design: Danuta Szyszka Cover photo: Sebastian Bożek Oficyna Wydawnicza Politechniki Wrocławskiej Wybrzeze Wyspianskiego 27 50-370 Wroclaw Any part of this publication can be used in any form by any means provided that the usage is acknowledged by the citation: Drzymala, J., Mineral Processing, Foundations of theory and practice of minerallurgy, Oficyna Wydawnicza PWr., 2007, www.ig.pwr.wroc.pl/minproc ISBN 978-83-7493-362-9 Contents Introduction ....................................................................................................................9 Part I Introduction to mineral processing .....................................................................13 1. From the Big Bang to mineral processing................................................................14 1.1. The formation of matter ...................................................................................14 1.2. Elementary particles.........................................................................................16 1.3. Molecules .........................................................................................................18 1.4. Solids................................................................................................................19 -
Fluid Mixing and the Deep Biosphere of a Fossil Lost City-Type Hydrothermal System at the Iberia Margin
Fluid mixing and the deep biosphere of a fossil Lost City-type hydrothermal system at the Iberia Margin Frieder Kleina,1, Susan E. Humphrisb, Weifu Guob, Florence Schubotzc, Esther M. Schwarzenbachd, and William D. Orsia aDepartment of Marine Chemistry and Geochemistry, Woods Hole Oceanographic Institution, Woods Hole, MA 02543; bDepartment of Geology and Geophysics, Woods Hole Oceanographic Institution, Woods Hole, MA 02543; cDepartment of Geosciences and Center for Marine Environmental Sciences, University of Bremen, 28334 Bremen, Germany; and dDepartment of Geosciences, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061 Edited by David M. Karl, University of Hawaii, Honolulu, HI, and approved August 4, 2015 (received for review March 7, 2015) Subseafloor mixing of reduced hydrothermal fluids with seawater is aging, brucite undersaturated in seawater dissolves and aragonite believed to provide the energy and substrates needed to support recrystallizes to calcite (7). deep chemolithoautotrophic life in the hydrated oceanic mantle (i.e., Actively venting chimneys host a microbial community with a serpentinite). However, geosphere-biosphere interactions in serpen- relatively high proportion of methanogenic archaea (the Lost tinite-hosted subseafloor mixing zones remain poorly constrained. City Methanosarcinales), methanotrophic bacteria, and sulfur- Here we examine fossil microbial communities and fluid mixing oxidizing bacteria, whereas typical sulfate-reducing bacteria are processes in the subseafloor of a Cretaceous Lost City-type hydro- rare (8–10). Geochemical evidence for significant microbial sulfate thermal system at the magma-poor passive Iberia Margin (Ocean reduction in basement lithologies and distinct microbial commu- Drilling Program Leg 149, Hole 897D). Brucite−calcite mineral assem- nities in Lost City vent fluids and chimneys suggest that subsurface blages precipitated from mixed fluids ca. -
Infrare D Transmission Spectra of Carbonate Minerals
Infrare d Transmission Spectra of Carbonate Mineral s THE NATURAL HISTORY MUSEUM Infrare d Transmission Spectra of Carbonate Mineral s G. C. Jones Department of Mineralogy The Natural History Museum London, UK and B. Jackson Department of Geology Royal Museum of Scotland Edinburgh, UK A collaborative project of The Natural History Museum and National Museums of Scotland E3 SPRINGER-SCIENCE+BUSINESS MEDIA, B.V. Firs t editio n 1 993 © 1993 Springer Science+Business Media Dordrecht Originally published by Chapman & Hall in 1993 Softcover reprint of the hardcover 1st edition 1993 Typese t at the Natura l Histor y Museu m ISBN 978-94-010-4940-5 ISBN 978-94-011-2120-0 (eBook) DOI 10.1007/978-94-011-2120-0 Apar t fro m any fair dealin g for the purpose s of researc h or privat e study , or criticis m or review , as permitte d unde r the UK Copyrigh t Design s and Patent s Act , 1988, thi s publicatio n may not be reproduced , stored , or transmitted , in any for m or by any means , withou t the prio r permissio n in writin g of the publishers , or in the case of reprographi c reproductio n onl y in accordanc e wit h the term s of the licence s issue d by the Copyrigh t Licensin g Agenc y in the UK, or in accordanc e wit h the term s of licence s issue d by the appropriat e Reproductio n Right s Organizatio n outsid e the UK. Enquirie s concernin g reproductio n outsid e the term s state d here shoul d be sent to the publisher s at the Londo n addres s printe d on thi s page. -
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. -
United States Patent (11) 3,615,174
United States Patent (11) 3,615,174 72 Inventor William J. Lewis 3,342,548 9/1967 Macey....... A. 2319 X South Ogden, Utah 3,432,031 3/1969 Ferris........................... 209/166 X 21 Appl. No. 740,886 FOREIGN PATENTS 22, Filed June 28, 1968 45 Patented Oct. 26, 1971 1,075,166 4f1954 France ......................... 209/66 (73) Assignee NL Industries, Inc. OTHER REFERENCES New York, N.Y. Chem. Abst., Vol. 53, 1959, 9587e I & EC, Vol. 56, 7, Jy '64, 61 & 62. Primary Examiner-Frank W. Lutter 54 PROCESSFOR THE SELECTIVE RECOVERY OF Assistant Examiner-Robert Halper POTASSUMAND MAGNESUMWALUES FROM Attorney-Ward, McElhannon, Brooks & Fitzpatrick AQUEOUSSALT SOLUTIONS CONTAINING THE SAME 11 Claims, 4 Drawing Figs. ABSTRACT: Kainite immersed in brine in equilibrium con 52) U.S. Cl........................................................ 23138, verted to carnalite by cooling to about 10 C. or under. Car 209/11, 209/166,23191, 22/121 nallite so obtained purified by cold flotation. Purified carnal (5) Int. Cl......................................................... B03b 1100, lite water leached to yield magnesium chloride brine and B03d 1102, C01f 5126 potassium chloride salt. Latter optionally converted to potas 50 Field of Search............................................ 209/166,3, sium sulfate by reaction with kainite, or by reacting the carnal 10, 11; 23.19, 38, 121 lite with kainite. Naturally occurring brine concentrated to precipitate principally sodium chloride, mother liquor warm 56 References Cited concentrated to precipitate kainite, cooled under mother UNITED STATES PATENTS liquor for conversion to carnallite. A crude kainite fraction 2,479,001 8/1949 Burke........................... 23.191 purified by warm flotation and a crude carnallite fraction pu 2,689,649 9, 1954 Atwood.... -
OCCURRENCE of BROMINE in CARNALLITE and SYLVITE from UTAH and NEW MEXICO* Manrr Loursp Lrnosonc
OCCURRENCE OF BROMINE IN CARNALLITE AND SYLVITE FROM UTAH AND NEW MEXICO* Manrr Loursp LrNosonc ABSTRACT Both carnallite and sylvite from Eddy County, New Mexico, contain 0.1 per cent of bromine. The bromine content of these minerals from Grand county, utah, is three times as great. No bromine was detected in halite, polyhalite, l5ngbeinite, or anhydrite from New Mexico. Iodine was not detected in any of these minerals. on the basis of the bromine content of the sylvite from New Mexico, it is calculated that 7,000 tons of bromine were present in potash salts mined from the permian basin during the period 1931 to 1945. INrnooucrroN The Geological Survey has previously made tests for bromine and iodine in core samples of potash salts from New Mexico.r Bromine was found to be present in very small amounts. No systematic quantitative determinations were made, nor was the presenceof bromine specificalry correlated with quantitative mineral composition. Sections of potash core from four recently drilled wells and selected pure saline minerals from Eddy County, New Mexico, together with two cores from Grand County, Utah, were therefore analyzed for their bromine and iodine content. The percentage mineral composition was then correlated with the bromine content. rt was found that bromine was restricted to carnall- ite and sylvite. fodine was not detected in any of the samples analyzed. If present, its quantity must be less than .00570. Brine and sea water are the present commercial sourcesof bromine in the United States, though both Germany and U.S.S.R. have utilized potash salts as a source of bromine. -
DOGAMI Short Paper 8, Strategic and Critical Minerals: a Guide for Oregon
STATE OF OREGON DEPARTMENT OF GEOLOGY AND MINERAL INDUSTRIES 702 Woodlark Building Portland, Oregon G M I SHORT PAPI:R No. 8 STRATEGIC AND CRITICAL MINERALS A GUIDE lOR OREGON PROSPECTORS. By Lloyd w. Staples; Ph.D, A••latant Proteaaor ot Geology University ot Oregon . • STATE GOVIEIIINING BOAIIID W. H. ITRAYIER, CHAIIIMAN . BAKU ALBIEIIIT BURC:H MIEDP'OIID IE MACNAUGHTON ••• PDIIT\.ANO EARL K. NIXON DIIIIIECTOIII PRICIE 15 CIENTI I Oat lORD In noraal tia•• ao1t pro•p•otor• look tor gold, 1inoe that aetal u1ually otter• the �uiok••t reward and i• generally tither •a•1ly reoogn1�•d or the or• 1• •usoept• 1ble or •••Y detera1nat1on. Pro1peotor11 ln general, thus gain llttlt or no experl tno• with other •inerai• who•• peaoetlae aarkttl otter little tnoentlve tor ltaroh tor new depo1it1. Under war oondltion• th••• aineral11 needed tor produotion ot war aat erial•, beooae ot priae iaportanoe and an in1i1tent deaand i1 created tor intoraation oonoernins ooourrenoe11 aineral oharaoteri1tio11 u1e1 and aarket1. fhe Dtpartaent i1 publllhins thil paper to help aeet thil deaand in1otar &I Oreson i1 �ono�rned. Dr. Staple• 11 tlptoially qualititd to write on the lubJeot or 1trateg1o aineral1. In rtoent rear• auoh ot hll work, both 1n private praotioe and 1n teaohing1 hat been oonoerntd with thll tubJeot. It 11 boptd that tht paptr will bt ot aattrial &1111t¬ to Oregon pro1ptotor1 &1 well al to 1aall operator• who have turned their attention troa gold aintns to thole alneral depo1it1 e11ential tor war netdl. It i1 believed that 1ohool1 will al1o t1nd the paper intoraatlve and tiaely. -
Anomalously High Cretaceous Paleobrine Temperatures: Hothouse, Hydrothermal Or Solar Heating?
minerals Article Anomalously High Cretaceous Paleobrine Temperatures: Hothouse, Hydrothermal or Solar Heating? Jiuyi Wang 1,2 ID and Tim K. Lowenstein 2,* 1 MLR Key Laboratory of Metallogeny and Mineral Assessment, Institute of Mineral Resources, Chinese Academy of Geological Sciences, Beijing 100037, China; [email protected] 2 Department of Geological Sciences and Environmental Studies, State University of New York, Binghamton, NY 13902, USA * Correspondence: [email protected]; Tel.: +1-607-777-4254 Received: 1 November 2017; Accepted: 9 December 2017; Published: 13 December 2017 Abstract: Elevated surface paleobrine temperatures (average 85.6 ◦C) are reported here from Cretaceous marine halites in the Maha Sarakham Formation, Khorat Plateau, Thailand. Fluid inclusions in primary subaqueous “chevron” and “cumulate” halites associated with potash salts contain daughter crystals of sylvite (KCl) and carnallite (MgCl2·KCl·6H2O). Petrographic textures demonstrate that these fluid inclusions were trapped from the warm brines in which the halite crystallized. Later cooling produced supersaturated conditions leading to the precipitation of sylvite and carnallite daughter crystals within fluid inclusions. Dissolution temperatures of daughter crystals in fluid inclusions from the same halite bed vary over a large range (57.9 ◦C to 117.2 ◦C), suggesting that halite grew at different temperatures within and at the bottom of the water column. Consistency of daughter crystal dissolution temperatures within fluid inclusion bands and the absence of vapor bubbles at room temperature demonstrate that fluid inclusions have not stretched or leaked. Daughter crystal dissolution temperatures are reproducible to within 0.1 ◦C to 10.2 ◦C (average of 1.8 ◦C), and thus faithfully document paleobrine conditions. -
Forsterite Dissolution and Magnesite Precipitation at Conditions Relevant for Deep Saline Aquifer Storage and Sequestration of Carbon Dioxide
Chemical Geology 217 (2005) 257–276 www.elsevier.com/locate/chemgeo Forsterite dissolution and magnesite precipitation at conditions relevant for deep saline aquifer storage and sequestration of carbon dioxide Daniel E. Giammara,T, Robert G. Bruant Jr.b, Catherine A. Petersb aDepartment of Civil Engineering and Environmental Engineering Science Program, Washington University, St. Louis, MO 63130, United States bProgram in Environmental Engineering and Water Resources, Department of Civil and Environmental Engineering, Princeton University, Princeton, NJ 08544, United States Received 30 April 2003; accepted 10 December 2004 Abstract The products of forsterite dissolution and the conditions favorable for magnesite precipitation have been investigated in experiments conducted at temperature and pressure conditions relevant to geologic carbon sequestration in deep saline aquifers. Although forsterite is not a common mineral in deep saline aquifers, the experiments offer insights into the effects of relevant temperatures and PCO2 levels on silicate mineral dissolution and subsequent carbonate precipitation. Mineral suspensions and aqueous solutions were reacted at 30 8C and 95 8C in batch reactors, and at each temperature experiments were conducted with headspaces containing fixed PCO2 values of 1 and 100 bar. Reaction products and progress were determined by elemental analysis of the dissolved phase, geochemical modeling, and analysis of the solid phase using scanning electron microscopy, infrared spectroscopy, and X-ray diffraction. The extent of forsterite dissolution increased with both increasing temperature and PCO2. The release of Mg and Si from forsterite was stoichiometric, but the Si concentration was ultimately controlled by the solubility of amorphous silica. During forsterite dissolution initiated in deionized water, the aqueous solution reached supersaturated conditions with respect to magnesite; however, magnesite precipitation was not observed for reaction times of nearly four weeks. -
12.109 Lecture Notes September 29, 2005 Thermodynamics II Phase
12.109 Lecture Notes September 29, 2005 Thermodynamics II Phase diagrams and exchange reactions Handouts: using phase diagrams, from 12.104, Thermometry and Barometry Fractional crystallization vs. equilibrium crystallization Perfect equilibrium – constant bulk composition, crystals + melt react, reactions go to equilibrium Perfect fractional – situation where reaction between phases is incomplete, melt entirely removed, etc. Because earth is not in equilibrium, we have interesting geology! Binary system = 2 component system Example: albite (Ab) and anorthite (An) solid solution Phase diagrams show the equilibrium case. Fractional crystallization would result in zoned crystal growth: The exchange of ions happens by solid state diffusion. If the crystal grows faster than ions can diffuse through it, the outer layers form with different compositions, thus we have a chemically zoned crystal. Olivine and plagioclase commonly grow this way. In crossed polarized light, you can see gradual extinction from the center, out to the edges of the crystal. This is also sometimes visible in clinopyroxene. Fractional crystallization preserves the original composition. The center zone has the composition of the crystal from the liquidus. The liquidus composition reveals the temperature of the liquid when it arrived at the final crystallization. Solvus, or miscibility gap – in system with solid solution, region of immiscibility (inability to mix) In Na-K feldspars, perthite results from unmixing of a single crystalline phase two coexisting phases with different compositions and same crystal structure As T goes down, two phases separate out (spinoidal decomposition) Feldspar system, see Bowen and Tuttle Thermometry and Barometry Thermobarometer Igneous and metamorphic rocks Uses composition of coexisting minerals to tell us something about T + P Liquidus minerals record temperature (if you can preserve the composition of the liquidus mineral. -
Experimental Investigations of the Reaction Path in the Mgo–CO2
Available online at www.sciencedirect.com Applied Geochemistry Applied Geochemistry 23 (2008) 1634–1659 www.elsevier.com/locate/apgeochem Experimental investigations of the reaction path in the MgO–CO2–H2O system in solutions with various ionic strengths, and their applications to nuclear waste isolation Yongliang Xiong *, Anna Snider Lord Sandia National Laboratories, Carlsbad Programs Group, 4100 National Parks Highway, Carlsbad, NM 88220, USA1 Received 26 June 2007; accepted 25 December 2007 Editorial handling by Z. Cetiner Available online 9 February 2008 Abstract The reaction path in the MgO–CO2–H2O system at ambient temperatures and atmospheric CO2 partial pressure(s), especially in high-ionic-strength brines, is of both geological interest and practical significance. Its practical importance lies mainly in the field of nuclear waste isolation. In the USA, industrial-grade MgO, consisting mainly of the mineral peri- clase, is the only engineered barrier certified by the Environmental Protection Agency (EPA) for emplacement in the Waste Isolation Pilot Plant (WIPP) for defense-related transuranic waste. The German Asse repository will employ a Mg(OH)2- based engineered barrier consisting mainly of the mineral brucite. Therefore, the reaction of periclase or brucite with car- bonated brines with high-ionic-strength is an important process likely to occur in nuclear waste repositories in salt forma- tions where bulk MgO or Mg(OH)2 will be employed as an engineered barrier. The reaction path in the system MgO–CO2– H2O in solutions with a wide range of ionic strengths was investigated experimentally in this study. The experimental results at ambient laboratory temperature and ambient laboratory atmospheric CO2 partial pressure demonstrate that hyd- romagnesite (5424) (Mg5(CO3)4(OH)2 Á 4H2O) forms during the carbonation of brucite in a series of solutions with differ- ent ionic strengths.