SODIUM COMPOUNDS (Excluding Salt)
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The American Journal of Science
THE AMERICAN JOURNAL OF SOIENOE. EDITOR: EDWARD S. DANA. ASSOCIATE EDITORS PROFESSORS GEO. L. GOODALE, JOHN TROWBRIDGE, H. P. BOWDITCH AND W. G. FARLOW, OF CAMBRIDGE, PROFESSORS O. C. MAHSH, A. E. VERRILL AND H. S. WILLIAMS, OF NEW HAVEN, PROFESSOR GEORGE F. BARKER, OF PHILADELPHIA, PROFESSOR H. A. ROWLAND, OF BALTIMORE, MR. J. S. DILLER, OF W ASHl~GTON. FOURTH SERIES. VOL. II-[WHOLE NUMBER, CLI!.] Nos. 7-12. JULY TO DEOEMBER, 1896. WITH SIX PLATES. NEW HAVEN, CONNECTICUT. 1896'. J. B. Pratt-Northupite, PirBsonite, etc. 123 , ART. ~V.-On Northupite; Pirs8onite, a new mineral j (}OI!flussite and IIanksite from Borax Lake, San Bernar dino County, Californi(t j by J. H. PRATT. INTRODUCTION. THE minerals to be described in this paper are from the remarkable locality of Borax Lake, San Bernardino County, California. They were broug-ht to the author's notice, in the fall of 1895, by Mr. Warren M. Foote of Philadelphia, who sent one of them, the northupite, tog-ether with some of the associ ated minerals, to the mineralogical laboratory of the Sheffield Scientific School, for chemical investigation. About the same time Mr. C. H. Northup of San Jose, CaL, sent some minerals from the same region to Prof. S. L. Penfield. Among them, gaylussite, hanksite and a third mineral, which has proved to be a new species, were identified. These same minerals were also observed among the specimens sent by Mr. Foote. Mr. Northup, in his letter of transmittal, stated that he had care fully saved all of the crystals of the new mineral, having observed that they were different from gaylnssite in habit, and that he believed they would prove to be a new and interesting species. -
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. -
Commodities, Part 5 Strontium, Sodium Sulfate, Trona (Soda Ash), Talc, Lithium, Summary Comments Safety Reminders
ME571/GEO571 Geology of Industrial Minerals Spring 2018 Commodities, Part 5 strontium, sodium sulfate, trona (soda ash), talc, lithium, summary comments Safety Reminders Commodity presentations—send me your powerpoints April 28 AIPG meeting and Field trip in afternoon (perlite mine or carbonatites) Research Projects presentation April 30 Finals, written Project due May 4 No class May 7 Strontium Strontium—introduction • Sr • 15th abundant element • does not occur naturally as an element, in compounds • No production in the United States since 1959 • celestite or celestine SrSO4 (same structure as barite) 56.4% Sr • strontianite SrCO3, 70.1% Sr Celesitite http://www.zeuter.com/~tburden Strontianite http://www.zeuter.com/~tburden Strontium and strontianite are named after Stronian, a village in Scotland near which the mineral was discovered in 1790 by Adair Crawford and William Cruickshank A critical mineral Strontium—uses • faceplate glass of color television picture tubes, 77% • ferrite ceramic magnets, 8% • pyrotechnics and signals, 9% – fireworks (red flame) – flares • other applications, 6% – refining zinc – optical materials Strontium—production USGS Mineral Yearbooks metric tons Strontium—geology • association with rocks deposited by the evaporation of sea water (evaporites) • igneous rocks • Brines • Barite and calcite must be removed— costly Sodium sulfate Sodium sulfate—introduction • disodium sulfate (Na2SO4), • inorganic chemical • Thenardite Na2SO4 • Hanksite Na22K(SO4)9(CO3)2Cl • Glauberite Na2Ca(SO4)2 Sodium sulfate—uses -
B Clifford Frondel
CATALOGUE OF. MINERAL PSEUDOMORPHS IN THE AMERICAN MUSEUM -B CLIFFORD FRONDEL BU.LLETIN OF THEAMRICANMUSEUM' OF NA.TURAL HISTORY. VOLUME LXVII, 1935- -ARTIC-LE IX- NEW YORK Tebruary 26, 1935 4 2 <~~~~~~~~~~~~~7 - A~~~~~~~~~~~~~~~, 4~~~~~~~~~~~~~~~~~~~~~~~~~~~~~4 4 4 A .~~~~~~~~~~~~~~~~~~~~~~~~~~4- -> " -~~~~~~~~~4~~. v-~~~~~~~~~~~~~~~~~~t V-~ ~~~~~~~~~~~~~~~~ 'W. - /7~~~~~~~~~~~~~~~~~~~~~~~~~~7 7-r ~~~~~~~~~-A~~~~ ~ ~ ~ ~ ~ ~ ~ ~ ~ -'c~ ~ ~ ' -7L~ ~ ~ ~ ~ 7 54.9:07 (74.71) Article IX.-CATALOGUE OF MINERAL PSEUDOMORPHS IN THE AMERICAN MUSEUM OF NATURAL HISTORY' BY CLIFFORD FRONDEL CONTENTS PAGE INTRODUCTION .................. 389 Definition.389 Literature.390 New Pseudomorphse .393 METHOD OF DESCRIPTION.393 ORIGIN OF SUBSTITUTION AND INCRUSTATION PSEUDOMORPHS.396 Colloidal Origin: Adsorption and Peptization.396 Conditions Controlling Peptization.401 Volume Relations.403 DESCRIPTION OF SPECIMENS.403 INTRODUCTION DEFINITION.-A pseudomorph is defined as a mineral which has the outward form proper to another species of mineral whose place it has taken through the action of some agency.2 This precise use of the term excludes the regular cavities left by the removal of a crystal from its matrix (molds), since these are voids and not solids,3 and would also exclude those cases in which organic material has been replaced by quartz or some other mineral because the original substance is here not a mineral. The general usage of the term is to include as pseudomorphs both petrifactions and molds, and also: (1) Any mineral change in which the outlines of the original mineral are preserved, whether this surface be a euhedral crystal form or the irregular bounding surface of an embedded grain or of an aggregate. (2) Any mineral change which has been accomplished without change of volume, as evidenced by the undistorted preservation of an original texture or structure, whether this be the equal volume replacement of a single crystal or of a rock mass on a geologic scale. -
Origin of the Kramer Borax Deposit, Boron, CA
A 50 year retrospective 1 OUTLINE 1. A brief history of borax 2. Kramer borax deposit a) Setting and Discovery b) Mineralogy of sedimentary borates c) Stratigraphy and Lithology d) Petrography and implications for geologic setting e) Solubility studies and modeling lake characteristics f) Comparable modern analogues 3. New evidence a) Turkish and Argentinian deposits b) Boron isotopic studies 4. Broader questions – Source water controls (thermal springs), B-As-Sb association, igneous-metamorphic controls on boron in thermal waters 2 Why give this talk? 1. Old (but rusty) material to me, new to most of you 2. Desire to see if ideas have changed in the past 50+ years. 3. Citation of my work even today suggests I did something right. 4. Wish to compare Kramer work with evidence from newer borate deposits in Turkey and South America 5. A wish to evaluate these ideas in light of new evidence using tools that weren’t available in 1964 6. A chance to ponder broader questions about boron’s geochemical cycle. 7. Work done so long ago that if you ask penetrating questions I can always plead a “senior moment” 3 What was unique about my research on the Kramer deposits? • Used a combination of geological tools (Field AND lab work – rare in 1964) • Stratigraphy, Petrography, and XRD based mineralogy • Experimental solubility studies of effects of other salts on Na-borate solubilities • Field studies of other possible borate environments (Borax Lake, Teels and Columbus Marsh, NV, Death Valley, Searles Lake) • Benefits of discussions with an all-star support team with similar interests (Mary Clark, Blair Jones, G.I. -
The Grystal Structure of Hanksite
American Mineralogist, Volume 58,pages 799-801,1973 The GrystalStructure of Hanksite Tnrlnlnu ARAKr,l,lNn Tlson Tntrx Departmentof Geologyand Geophysics,Uniuersity of Minnesota, Minneapolis, Minnesota 554 5 5 Abstract Hanksite, NaaK(COg)r(SOn)"C1, from Searles Lake, California, gave the space group P6s/m and the unit cell constants a - 10.465 and c - 21,191 A. Its structure was solved by three-dimensional Patterson synthesis and subsequent Fourier methods. The atomic co- ordinates and isotropic temperature factors were refined by full-matrix least-squares to R = 6.45 percentfor 1159reflections. The structure is characterized by chains of Na and K octahedra running parallel to the c-axis. These chains are connected by carbon and sulfur coordination groups, Introduction cell dimensionsare in good agreementwith those ( The mineralogy and the conditions of occurrence first reportedby Ramsdell 1939). of hanksite,NazsK(COe)2(SO4)ecl, at SearlesLake, Three-dimensionalintensities were collectedby a California, and the system Na-Cl-SOa-COs-H2O, generalinclination (Santoro and Zocchi, 1966) dif- which includeshanksite, have been extensivelystud- fractometerusing CuKc radiationon a crystalfrag- ied by severalauthors (Eugster and Smith, 1965; ment mountedfor a-axis rotation. All 1268 reflec- = Hardie and Eugster, l97O; Smith, Friedman, and tions were measuredup to sin 0 O.9245and were Matsuo, 1970). The possiblecrystal structure of correctedfor absorptionusing the methodintroduced hanksite, however, posed interesting questionsdue by Burnham (1966). The spacegroup of P6s/m to the unusual cation ratios in its chemicalcomposi- was concludedfrom the systematicabsences in the tion and the identity of its morphology and space 00t reflections,from the inequalities between hkl group with that of apatite. -
A Specific Gravity Index for Minerats
A SPECIFICGRAVITY INDEX FOR MINERATS c. A. MURSKyI ern R. M. THOMPSON, Un'fuersityof Bri.ti,sh Col,umb,in,Voncouver, Canad,a This work was undertaken in order to provide a practical, and as far as possible,a complete list of specific gravities of minerals. An accurate speciflc cravity determination can usually be made quickly and this information when combined with other physical properties commonly leads to rapid mineral identification. Early complete but now outdated specific gravity lists are those of Miers given in his mineralogy textbook (1902),and Spencer(M,i,n. Mag.,2!, pp. 382-865,I}ZZ). A more recent list by Hurlbut (Dana's Manuatr of M,i,neral,ogy,LgE2) is incomplete and others are limited to rock forming minerals,Trdger (Tabel,l,enntr-optischen Best'i,mmungd,er geste,i,nsb.ildend,en M,ineral,e, 1952) and Morey (Encycto- ped,iaof Cherni,cal,Technol,ogy, Vol. 12, 19b4). In his mineral identification tables, smith (rd,entifi,cati,onand. qual,itatioe cherai,cal,anal,ys'i,s of mineral,s,second edition, New york, 19bB) groups minerals on the basis of specificgravity but in each of the twelve groups the minerals are listed in order of decreasinghardness. The present work should not be regarded as an index of all known minerals as the specificgravities of many minerals are unknown or known only approximately and are omitted from the current list. The list, in order of increasing specific gravity, includes all minerals without regard to other physical properties or to chemical composition. The designation I or II after the name indicates that the mineral falls in the classesof minerals describedin Dana Systemof M'ineralogyEdition 7, volume I (Native elements, sulphides, oxides, etc.) or II (Halides, carbonates, etc.) (L944 and 1951). -
A Mineral Physics Perspective a Dissertation Submitted in Partial
UNIVERSITY OF CALIFORNIA Los Angeles Carbon in the Deep Earth: A Mineral Physics Perspective A dissertation submitted in partial satisfaction of the requirements for the degree Doctor of Philosophy in Geochemistry by Sarah Eileen Maloney Palaich 2016 © Copyright by Sarah Eileen Maloney Palaich 2016 ABSTRACT OF THE DISSERTATION Carbon in the Deep Earth: A Mineral Phyiscs Perspective by Sarah Eileen Maloney Palaich Doctor of Philosophy in Geochemistry University of California, Los Angeles, 2016 Professor Abby Kavner, Co-Chair Professor Craig E. Manning, Co-Chair Carbon is an essential component to life on Earth, and plays a role in the carbon cycle at the surface of the Earth. Beyond these surface interactions lies the deep carbon cycle. This cycle controls the flux of carbon subducting into the earth and provides clues as a possible carbon reservoir in the deep earth. The studies included in this dissertation examine various forms of carbonate under high pressure, high temperature conditions found in the deep earth. Carbon is subducted as carbonate in calcite, aragonite and dolomite, as elemental carbon or as CO2. To achieve these the high pressures experienced by subducting material, diamond anvil cells are ii used to expose milligrams of material to extremem conditions. The experiments detailed here were conducted using a wide range of diamond anvil cell techniques and the data was collected at numerous synchrotron and neutron diffraction facilities across the globe including the Advanced Light Source, Lawrence Berekely National Laboratory, the Spallation Neutron Source, Oak Ridge National Laboratory and the European Synchrotron Radiation Facility, Grenoble France. These experiments are the result of fruitful collaborations that brought scientist from around the globe together to study the thermoelastic properties of carbonate and CO2. -
Pink Halite (With Nahcolite) from Searles Lake (Actual Size 13.0 X 11.4Cm) the Holiday Party at the Pierce's on Sat. 12/05
DELVINGS __________________________________________________________ Volume LXVIII Number 12 December 2015 Pink Halite (with Nahcolite) from Searles Lake (actual size 13.0 x 11.4cm) Photo from Wikimedia Commons courtesy Rob Lavinsky/iRocks.com The holiday party at the Pierce’s on Sat. 12/05 is our December meeting Shopping opportunity at the Jewel Tunnel Imports warehouse – Sat 12/05: 10-4 ©Delvers Gem & Mineral Society, Inc.- a 501 (c)(3) organization- 1001 West Lambert Rd. #18, La Habra, CA 90631-1378 Saturday, December 5th – the Delvers Holiday Party, and Installation of Officers 1318 North Kroeger Ave., Fullerton 4:30 to 5:30 Hors d'oeuvre and crafts; 5:30 Sit-down Dinner Chuck Pierce: 714-595-3862, [email protected] We will have an ugly ornament exchange this year. To participate, bring a wrapped ugly ornament. One approach from the 91 Frwy is to take Raymond Avenue north. Turn left onto Melody Lane, after 0.2 miles turn right onto Kroeger Ave Jewel Tunnel Wholesale Warehouse Saturday December 5 th, 10 AM – 4 PM Members and friends of the Delvers Gem and Mineral Society are invited to attend an open-house at Jewel Tunnel Imports on Saturday December 5th, 2015. Starving students and others will be fed. Unattended children will be sold as slaves. Jewel Tunnel Imports is a leading wholesale distributor of mineral specimens, crystals, fossils, tumbled stones and many different kinds of lapidary items like balls, eggs, jewelry etc. made from different minerals. We have a warehouse in excess of 10,000 sq. feet full of mineral related natural history items, perhaps the largest of its kind in the United States. -
Character and Distribution of Nonclastic Minerals in the Searles Lake Evaporite Deposit California
Character and Distribution of Nonclastic Minerals in the Searles Lake Evaporite Deposit California By GEORGE I. SMITH and DAVID V. HAINES I CONTRIBUTIONS TO GENERAL GEOLOGY GEOLOGICAL SURVEY BULLETIN 1181-P Prepared in cooperation with the State of California, Resources Agency, ' Department of Conservation, Division of Mines and Geology -A UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1964 UNITED STATES DEPARTMENT OF THE INTERIOR STEWART L. UDALL, Secretary GEOLOGICAL SURVEY Thomas B. Nolan, Director The U.S. Geological Survey Library catalog card for this publication appears after page P58. For sale by the Superintendent of Documents, U.S. Government Printing Office Washington, D.C. 20402 CONTENTS Page Abstract..---.---------------------------------------------------- PI Introduction-____________-___-___----_--_-______-____--_______-___ 3 Acknowledgments ____-_____---_-__--__--_----__-_______---____..__- 4 Mineralogy __________-_---_---------_-_--_----_-------_--__-_-____ 6 , Minerals associated with saline layers____________________________ 8 Aphthitalite.. __-____---_----_---_--___---_---__-_________ 8 Borax-----.--------------------------------------.------- 10 Burkeite__.______--____-_.._-___-._-__.____..._..______ 12 Halite ------------------------------------------------- 14 Hanksite.-_------------_-----_-------__----------_----__- 16 Nahcolite__-___-_---_-_______-___-___---_____-___-_-____ 18 ^ Sulfohalite-.--------------------------------------------- 19 Teepleite._-----------------_----_------_-------_---_-.-.- 20 ,- -
Co3 47 » Scale of Miles HCO3 5 » CI 154 » 62 » Fig
TYCHITE AND NORTHUPITE FROM LAKE KATWE, UGANDA P. H. NIXON, W. H. MORTON and O. von KNORRING NIXON, P. H., MORTON, W. H. and von KNORRING, O 1971: Tychite and northupite from Lake Katwe, Uganda. Bull. Geol. Soc. Finland 43, 125—130. P. H. Nixon and W. H. Morton, Formerly of Uganda Geological Survey. O. von Knorring, University of Leeds, England. Introduction A good description of Lake Katwe has been given by Wayland (1934) and Holmes (1956) Lake Katwe is the largest of the saline crater has described the volcanic tuffs and ejectamenta lakes within the Katwe-Kikorongo volcanic connected with the crater. field in Uganda (Figs. 1—3). It lies on the floor During 1967 a programme of drilling was of the Western Rift Valley and south-east of the undertaken by the Geological Survey of Uganda Ruwenzori range. This is an unusually dry area missing much of the rain that falls on Ruwenzori and on the country east of the Buhwezu scarp. Lake Katwe consists of at least three intersecting explosion craters blown through subaqueous volcanic tuffs. The total lake area is at present about 2*4 km2, comprising a circular part of I km across and a smaller embayment to the east formed from an adjacent crater. The third and smaller crater is permanently dry. Lying only 250 m from Lake Edward, the surface of the crater lake is some 30 m below the latter's. Radiocarbon dating indicates that most of the evaporites have accumulated within the last II 000 years. V The brine of Lake Katwe has the following / y u aXu composition: Na 150 g/litre K 37 » co3 47 » Scale of Miles HCO3 5 » CI 154 » 62 » Fig. -
Rrelative Salt in Panamint Valley
Mineral. Soc. Amer. Spec. Pap. 3,307-319 (1970). BROMIDE GEOCHEMISTRY OF SOME NON-MARINE SALT DEPOSITS IN THE SOUTHERN GREAT BASIN WILLIAM T. HOLSER Chevron Oil Field Research Company, La Habra, California 90631 ABSTRACT The Wisconsin Upper Salt and Lower Salt in Searles Lake regularly contain about 50 ppm Br, compared to a mean of 20 ppm in the Early to Late Pleistocene Mixed Layer in Searles and the correlative salt in Panamint Valley. At least one period of dessication is suggested by high bromide in unit C of the Mixed Layer. Bromide in both the Pliocene Virgin Valley and Avawatz Mountain salt rocks is 6 to 10 ppm. This low range is consistent with derivation from older marine salt rocks eroded from the Colorado Plateau by an ancestral Colorado River. The Wisconsin salts at Searles accumulated at a rate possibly consistent with the recent flux of chloride in the Owens River, but these rates are several times the present input of chloride into the entire Owens drainage, including atmospheric precipitation and a small contribution from thermal springs. The halides may have been held over in Pliocene sediments such as the Waucobi-Coso lake beds. Various lines of evidence about Pliocene geography of this area admit the possi- bility that the Waucobi-Coso sediments may also have received some of their halides from an eastern source of marine evaporites either by a westward-flowing river or by westward-moving weather systems. INTRODUCTION MULTICYCLE FRESH- WATER 2nd- The general geochemical evolution of lake waters in the CYCLE EVAPORITES BRINE Great Basin was first developed by Hutchinson (1957), and ( with more detailed evidence by Jones (1966).