Brine Evolution in Qaidam Basin, Northern Tibetan Plateau, and the Formation of Playas As Mars Analogue Site
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Potash Case Study
Mining, Minerals and Sustainable Development February 2002 No. 65 Potash Case Study Information supplied by the International Fertilizer Industry Association This report was commissioned by the MMSD project of IIED. It remains the sole Copyright © 2002 IIED and WBCSD. All rights reserved responsibility of the author(s) and does not necessarily reflect the views of the Mining, Minerals and MMSD project, Assurance Group or Sponsors Group, or those of IIED or WBCSD. Sustainable Development is a project of the International Institute for Environment and Development (IIED). The project was made possible by the support of the World Business Council for Sustainable Development (WBCSD). IIED is a company limited by guarantee and incorporated in England. Reg No. 2188452. VAT Reg. No. GB 440 4948 50. Registered Charity No. 800066 1 Introduction 2 2 Global Resources and Potash Production 3 3 The use of potassium in fertilizer 4 3.1 Potassium Fertilizer Consumption 4 3.2 Potassium fertilization issues 6 Appendix A 8 1 Introduction Potash and Potassium Potassium (K) is essential for plant and animal life wherein it has many vital nutritional roles. In plants, potassium and nitrogen are the two elements required in greatest amounts, while in animals and humans potassium is the third most abundant element, after calcium and phosphorus. Without sufficient plant and animal intake of potassium, life as we know it would cease. Human and other animals atop the food chain depend upon plants for much of their nutritional needs. Many soils lack sufficient quantities of available potassium for satisfactory yield and quality of crops. For this reason available soil potassium levels are commonly supplemented by potash fertilization to improve the potassium nutrition of plants, particularly for sustaining production of high yielding crop species and varieties in modern agricultural systems. -
Mirabilite Na2so4 • 10H2O C 2001-2005 Mineral Data Publishing, Version 1
Mirabilite Na2SO4 • 10H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. Crystals short to long prismatic, with complex form development, also crude, to 10 cm, in interlocking masses; crystalline, granular to compact massive, commonly as efflorescences. Twinning: Rare on {001} or {100}. Physical Properties: Cleavage: On {100}, perfect; on {010} and {001}, good to fair. Fracture: Conchoidal. Hardness = 1.5–2.5 D(meas.) = 1.464 D(calc.) = 1.467 Quickly dehydrates to th´enarditein dry air; very soluble in H2O, taste cool, then saline and bitter. Optical Properties: Transparent to opaque. Color: Colorless to white; colorless in transmitted light. Streak: White. Luster: Vitreous. Optical Class: Biaxial (–). Orientation: X = b; Z ∧ c =31◦. Dispersion: r< v,strong, crossed. α = 1.391–1.394 β = 1.394–1.396 γ = 1.396–1.398 2V(meas.) = 75◦560 Cell Data: Space Group: P 21/c (synthetic). a = 11.512(3) b = 10.370(3) c = 12.847(2) β = 107.789(10)◦ Z=4 X-ray Powder Pattern: Synthetic. (ICDD 11-647). 5.49 (100), 3.21 (75), 3.26 (60), 3.11 (60), 4.77 (45), 3.83 (40), 2.516 (35) Chemistry: (1) (2) SO3 25.16 24.85 Na2O 18.67 19.24 H2O 55.28 55.91 Total 99.11 100.00 • (1) Kirkby Thore, Westmoreland, England. (2) Na2SO4 10H2O. Occurrence: Typically in salt pans, playas, and saline lakes, where deposition may be seasonal, and bedded deposits formed therefrom; rarely in caves and lava tubes; in volcanic fumaroles; a product of hydrothermal sericitic alteration; a post-mining precipitate. -
Damage to Monuments from the Crystallization of Mirabilite, Thenardite and Halite: Mechanisms, Environment, and Preventive Possibilities
Eleventh Annual V. M. Goldschmidt Conference (2001) 3212.pdf DAMAGE TO MONUMENTS FROM THE CRYSTALLIZATION OF MIRABILITE, THENARDITE AND HALITE: MECHANISMS, ENVIRONMENT, AND PREVENTIVE POSSIBILITIES. E. Doehne1, C. Selwitz2, D. Carson1, and A. de Tagle1, 1The Getty Conservation Institute, 1200 Getty Center Drive, Suite 700, Los Angeles, CA 90049, USA, TEL: (310) 440 6237, FAX: 310 440 7711, Email: [email protected], 23631 Surfwood road, Malibu, CA, 90265, USA. Introduction: "In time, and with water, everything sulfate through columns of limestone. The limestones changes." ---Leonardo da Vinci were oolitic Monks Park stone where 90% of its pores The crystallization of soluble salts in porous building measured between 0.05-0.80 microns and Texas materials is a widespread weathering process that re- Creme, a fossilferous stone with 90% of its pore size sults in damage to important monuments and archaeo- distribution measuring between 0.5 and 3.0 microns. logical sites [1]. Salt weathering by thenardite (sodium In the absence of modifiers, sodium chloride passage sulfate) and mirabilite (sodium sulfate decahydrate) is through Monks Park limestone gave predominantly especially destructive, yet is still not fully understood subflorescence with mild edge erosion while sodium [2]. Halite (sodium chloride) in contrast, is one of the sulfate mainly effloresced and severely damaged the least damaging salts [3]. Previous work has also dem- stone column. With Texas Creme limestone, essen- onstrated the importance of airflow in salt weathering tially only efflorescence occurred with either salt and [4]. Here we present new data that help explain why there was little or no stone damage. sodium sulfate is so damaging and also show how Most crystallization inhibitors--used in industry to crystallization modifiers and changes in airflow can prevent scaling by promoting high supersaturation reduce salt damage in laboratory experiments. -
Mining Methods for Potash
Potash—A Vital Agricultural Nutrient Sourced from Geologic Deposits Open File Report 2016–1167 U.S. Department of the Interior U.S. Geological Survey Cover. Photos of underground mining operations, Carlsbad, New Mexico, Intrepid Potash Company, Carlsbad West Mine. Potash—A Vital Agricultural Nutrient Sourced from Geologic Deposits By Douglas B. Yager Open File Report 2016–1167 U.S. Department of the Interior U.S. Geological Survey U.S. Department of the Interior SALLY JEWELL, Secretary U.S. Geological Survey Suzette M. Kimball, Director U.S. Geological Survey, Reston, Virginia: 2016 For more information on the USGS—the Federal source for science about the Earth, its natural and living resources, natural hazards, and the environment—visit http://www.usgs.gov or call 1–888–ASK–USGS. For an overview of USGS information products, including maps, imagery, and publications, visit http://store.usgs.gov/. Any use of trade, firm, or product names is for descriptive purposes only and does not imply endorsement by the U.S. Government. Although this information product, for the most part, is in the public domain, it also may contain copyrighted materials as noted in the text. Permission to reproduce copyrighted items must be secured from the copyright owner. Suggested citation: Yager, D.B., 2016, Potash—A vital agricultural nutrient sourced from geologic deposits: U.S. Geological Survey Open- File Report 2016–1167, 28 p., https://doi.org/10.3133/ofr20161167. ISSN 0196-1497 (print) ISSN 2331-1258 (online) ISBN 978-1-4113-4101-2 iii Acknowledgments The author wishes to thank Joseph Havasi of Compass Minerals for a surface tour of their Great Salt Lake operations. -
Mineral Commodity Summareis 2013
U.S. Department of the Interior U.S. Geological Survey MINERAL COMMODITY SUMMARIES 2013 Abrasives Fluorspar Mercury Silver Aluminum Gallium Mica Soda Ash Antimony Garnet Molybdenum Sodium Sulfate Arsenic Gemstones Nickel Stone Asbestos Germanium Niobium Strontium Barite Gold Nitrogen Sulfur Bauxite Graphite Peat Talc Beryllium Gypsum Perlite Tantalum Bismuth Hafnium Phosphate Rock Tellurium Boron Helium Platinum Thallium Bromine Indium Potash Thorium Cadmium Iodine Pumice Tin Cement Iron and Steel Quartz Crystal Titanium Cesium Iron Ore Rare Earths Tungsten Chromium Iron Oxide Pigments Rhenium Vanadium Clays Kyanite Rubidium Vermiculite Cobalt Lead Salt Wollastonite Copper Lime Sand and Gravel Yttrium Diamond Lithium Scandium Zeolites Diatomite Magnesium Selenium Zinc Feldspar Manganese Silicon Zirconium U.S. Department of the Interior KEN SALAZAR, Secretary U.S. Geological Survey Marcia K. McNutt, Director U.S. Geological Survey, Reston, Virginia: 2013 Manuscript approved for publication January 24, 2013. For more information on the USGS—the Federal source for science about the Earth, its natural and living resources, natural hazards, and the environment— visit http://www.usgs.gov or call 1–888–ASK–USGS. For an overview of USGS information products, including maps, imagery, and publications, visit http://www.usgs.gov/pubprod For sale by the Superintendent of Documents, U.S. Government Printing Office Mail: Stop IDCC; Washington, DC 20402–0001 Phone: (866) 512–1800 (toll-free); (202) 512–1800 (DC area) Fax: (202) 512–2104 Internet: bookstore.gpo.gov Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government. Although this report is in the public domain, permission must be secured from the individual copyright owners to reproduce any copyrighted material contained within this report. -
Fertilizer Production Expertise HPD® Evaporation and Crystallization
Fertilizer Production Expertise HPD® Evaporation and Crystallization WATER TECHNOLOGIES Fertilizer Expertise Case Study: Veolia NPK Fertilizers HPD® Evaporation and Crystallization systems from Veolia Research & Development NPK Process Capabilities Water Technologies provide innovative process solutions for large-scale fertilizer production facilities worldwide. IC Potash Corp. (ICP) - Sulfate of Potash (SOP) These systems allow production of a wide range of high-quality fertilizer products from natural sources (mined or solution mined deposits) or by-product streams from other processes that include: Chlorine / • Ammonium sulfate • Mono potassium phosphate Raw Materials Natural Gas Sulfur Phosphate Rock Hydrogen Gas Potash Source • Ammonium nitrate (MKP) • Potassium chloride (MOP) • Sodium nitrate • Potassium sulfate (SOP) • Phosphoric acid merchant/ technical/food/electrical • Monoammonium phosphate (MAP) grade ICP's Ochoa Mine project (New Mexico, USA) is • Diammonium phosphate • Potassium carbonate (DAP) • Potassium nitrate projected to produce approximately 714,000 TPY Ammonia Plant Sulfuric Acid Rock Grinding Hydrochloric Acid of Sulfate of Potash (SOP-K SO ) from Polyhalite • Epsom salt: Magnesium • Calcium phosphate 2 4 Plant Plant Plant ore (K SO .MgSO .2CaSO .2H O) for more than 50 sulfate heptahydrate • Calcium sulfate 2 4 4 4 2 years. • Magnesium sulfate • Calcium chloride monohydrate Veolia was selected to refine, confirm, and validate the overall ICP process utilizing HPD® Evaporation and Crystallization technologies through a series of bench and pilot-scale testing programs performed in Veolia’s in-house testing facility. The scope of the testing extended lants from the ore P leaching to the SOP crystallization process including Nitric Acid Plant Phosphoric Acid PlantPotassium Chloride Plant crystallization/redissolution of leonite (K2SO4. -
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. -
A 94–10Ka Pollen Record of Vegetation Change in Qaidam Basin
Palaeogeography, Palaeoclimatology, Palaeoecology 431 (2015) 43–52 Contents lists available at ScienceDirect Palaeogeography, Palaeoclimatology, Palaeoecology journal homepage: www.elsevier.com/locate/palaeo A94–10 ka pollen record of vegetation change in Qaidam Basin, northeastern Tibetan Plateau Haicheng Wei a,QishunFana, Yan Zhao b,HaizhouMaa, Fashou Shan a,FuyuanAna,QinYuana a Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China b Institute of Geographic Sciences and Natural Resources Research, Chinese Academy of Sciences, Beijing 100101, China article info abstract Article history: Drill core (ISL1A) was obtained from the Qarhan Salt Lake in central eastern Qaidam Basin, northeastern Tibetan Received 19 May 2014 Plateau (NE TP). Fossil pollen and the lithology of the core sediment were analyzed in conjunction with AMS 14C Received in revised form 27 March 2015 and 230Th dating. The results indicated that Artemisia and Chenopodiaceae dominated the steppe/desert steppe Accepted 24 April 2015 vegetation developed around the lake between 94 and 51.2 ka, corresponding with the organic-rich silty clay de- Available online 4 May 2015 posited in the core sediments. Pediastrum continuously appeared in the core sediments between 94 and 51.2 ka, Keywords: indicating freshwater to oligohaline conditions of the paleo-Qarhan Lake during the late marine isotope stage Pollen record (MIS) 5, MIS 4, and early MIS 3. During the 51.2 to 32.5 ka period, Ephedra dominated shrub-desert vegetation Climate change expanded in the basin, while, Pediastrum disappeared in the core sediments. The core sediments consisted of in- Qaidam Basin terbedded layers of halite silt and clay-rich halite between 51.2 and 32.5 ka, signifying a shift toward drier hydro- Late Pleistocene logic conditions. -
C:\Documents and Settings\Alan Smithee\My Documents\MOTM
I`mt`qx1//4Lhmdq`knesgdLnmsg9Fk`tadqhsd Glauberite is something of a paradox among minerals, better known for specimens in which it is not present, than for those in which it is. In other words, glauberite is one of the Mineral Kingdom’s most widely pseudomorphed species, as the write-up will explain. We’ll also talk about the former Mineral of the Month Club. OGXRHB@K OQNODQSHDR Chemistry: Na2Ca(SO4)2 Sodium Calcium Sulfate Class: Sulfates Sub-Group: Anhydrous Sulfates Group: Glauberite Crystal System: Monoclinic Crystal Habits: Tabular or prismatic; steeply inclined, wedge-to-tabular-shaped dipyramidal crystals, sometimes with rounded edges; striated on several faces; pseudomorphic replacement common; also forms epimorphic Figure 1. Glauberite crystal. crystals, in which a second mineral encrusts the original glauberite crystals which then dissolve away to leave hollow, outer shells. Color: Colorless in unaltered crystals; altered or partially altered crystals yellowish or grayish, often white due to a powdery, efflorescent coating that forms upon prolonged exposure to dry air. Luster: Vitreous when free of efflorescent coating Transparency: Transparent to translucent; unaltered crystals usually transparent Streak: White Refractive Index: 1.51-1.53 Cleavage: Perfect in one direction Fracture: Very brittle, producing small conchoidal fragments Hardness: 2.5-3.0 Specific Gravity: 2.7-2.8 Luminescence: None Distinctive Features and Tests: Occurrence in evaporate deposits and association with such minerals as halite (sodium chloride, NaCl), calcite (calcium carbonate, CaCO3), thenardite (sodium sulfate, Na2SO4), gypsum (hydrous calcium sulfate, CaSO4AH2O). Sometimes confused with halite and calcite, but glauberite lacks halite’s pronounced cubic shape and dissolves more slowly in water. -
Present Response of Qarhan Salt Flat to the Watershed Hydroclimate: the Key to Understanding Past Conditions for Evaporitic Deposit Formation
Abstract by JunQing Yu oral presentation_15th East Eurasia International Workshop, Busan, Korea 2018 PRESENT RESPONSE OF QARHAN SALT FLAT TO THE WATERSHED HYDROCLIMATE: THE KEY TO UNDERSTANDING PAST CONDITIONS FOR EVAPORITIC DEPOSIT FORMATION JunQing Yu1,2*, Lisha Zhang1,2, Chunliang Gao1,2, Rongchang Hong1,3, Aiying Cheng1,2 1 Key Laboratory of Comprehensive and Highly Efficient Utilization of Salt Lake Resources, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China 2 Qinghai Provincial Key Laboratory of Geology and Environment of Salt Lakes, Qinghai Institute of Salt Lakes, Chinese Academy of Sciences, Xining 810008, China 3 University of Chinese Academy of Sciences, Beijing 100049, China Correspondence: [email protected]; Tel.: +86-971-630-7153 Qarhan Salt Flat is the largest potash deposit in China and covers an area of 5856 km2 of the Qaidam Basin in the nothern Tibet-Qinghai Plateau. Although efforts on the study of the evaporite deposit were tremendous in the past 60 years, answers to the following questions remained inconclusive: (1) the cause and commencement timing of the evaporitic deposition and (2) when and what resulted in the shift of evaporitic deposition to a playa environment. A deep paleo-lake prior to the evaporite deposit formation, as hypothesized by previous studies, is proven unlikely by increasing evidence from sedimentologic and geomorphic studies. Bieletan, the westernmost sub-playa of Qarhan today, did not belong to the uniform Qarhan Salt Flat until the beginning of the deposition of the top 20-m evaporitic sequence, based on both the configuration of evaporitic strata and the distribution pattern of the lithium deposit. -
Sodium Sulphate: Its Sources and Uses
DEPARTMENT OF THE INTERIOR HUBERT WORK, Secretary UNITED STATES GEOLOGICAL SURVEY GEORGE OTIS SMITH, Director Bulletin 717 SODIUM SULPHATE: ITS SOURCES AND USES BY ROGER C. WELLS WASHINGTON GOVERNMENT PRINTING OFFICE 1 923 - , - _, v \ w , s O ADDITIONAL COPIES OF THIS PUBLICATION MAY BE PBOCUKED FROM THE SUPERINTENDENT OF DOCUMENTS GOVERNMENT PRINTING OFFICE WASHINGTON, D. C. AT 5 CENTS PEE COPY PURCHASER AGREES NOT TO RESELL OR DISTRIBUTE THIS COPY FOR PROFIT. PUB. RES. 57, APPROVED MAY 11, 1922 CONTENTS. Page. Introduction ____ _____ ________________ 1 Demand 1 Forms ____ __ __ _. 1 Uses . 1 Mineralogy of principal compounds of sodium sulphate _ 2 Mirabilite_________________________________ 2 Thenardite__ __ _______________ _______. 2 Aphthitalite_______________________________ 3 Bloedite __ __ _________________. 3 Glauberite ____________ _______________________. 4- Hanksite __ ______ ______ ___________ 4 Miscellaneous minerals _ __________ ______ 5 Solubility of sodium sulphate *.___. 5 . Transition temperature of sodium sulphate______ ___________ 6 Reciprocal salt pair, sodium sulphate and potassium chloride____ 7 Relations at 0° C___________________________ 8 Relations at 25° C__________________________. 9 Relations at 50° C__________________________. 10 Relations at 75° and 100° C_____________________ 11 Salt cake__________ _.____________ __ 13 Glauber's salt 15 Niter cake_ __ ____ ______ 16 Natural sodium sulphate _____ _ _ __ 17 Origin_____________________________________ 17 Deposits __ ______ _______________ 18 Arizona . 18 -
Ulexite Nacab5o6(OH)6 • 5H2O C 2001-2005 Mineral Data Publishing, Version 1 Crystal Data: Triclinic
Ulexite NaCaB5O6(OH)6 • 5H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Triclinic. Point Group: 1. Rare as measurable crystals, which may have many forms; typically elongated to acicular along [001], to 5 cm, then forming fibrous cottonball-like masses; in compact parallel fibrous veins, and radiating and compact nodular groups. Twinning: Polysynthetic on {010} and {100}; possibly also on {340}, {230}, and others. Physical Properties: Cleavage: On {010}, perfect; on {110}, good; on {110}, poor. Fracture: Uneven across fiber groups. Tenacity: Brittle. Hardness = 2.5 D(meas.) = 1.955 D(calc.) = 1.955 Slightly soluble in H2O; parallel fibrous masses can act as fiber optical light pipes; may fluoresce yellow, greenish yellow, cream, white under SW and LW UV. Optical Properties: Transparent to opaque. Color: Colorless; white in aggregates, gray if included with clays. Luster: Vitreous; silky or satiny in fibrous aggregates. Optical Class: Biaxial (+). Orientation: X (11.5◦,81◦); Y (100◦,21.5◦); Z (107◦,70◦) [with c (0◦,0◦) and b∗ (0◦,90◦) using (φ,ρ)]. α = 1.491–1.496 β = 1.504–1.506 γ = 1.519–1.520 2V(meas.) = 73◦–78◦ Cell Data: Space Group: P 1. a = 8.816(3) b = 12.870(7) c = 6.678(1) α =90.36(2)◦ β = 109.05(2)◦ γ = 104.98(4)◦ Z=2 X-ray Powder Pattern: Jenifer mine, Boron, California, USA. 12.2 (100), 7.75 (80), 6.00 (30), 4.16 (30), 8.03 (15), 4.33 (15), 3.10 (15b) Chemistry: (1) (2) B2O3 43.07 42.95 CaO 13.92 13.84 Na2O 7.78 7.65 H2O 35.34 35.56 Total 100.11 100.00 • (1) Suckow mine, Boron, California, USA.