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AND THORIAN SYNCHYSITE-(Ce) from the NIEDERBOBRITZSCH GRANITE, ERZGEBIRGE, GERMANY: IMPLICATIONS for the DIFFERENTIAL MOBILITY of the LREE and Th DURING ALTERATION
67 The Canadian Mineralogist Vol. 38, pp. 67-79 (2000) CERITE-(Ce) AND THORIAN SYNCHYSITE-(Ce) FROM THE NIEDERBOBRITZSCH GRANITE, ERZGEBIRGE, GERMANY: IMPLICATIONS FOR THE DIFFERENTIAL MOBILITY OF THE LREE AND Th DURING ALTERATION HANS-JÜRGEN FÖRSTER§ GeoForschungsZentrum Potsdam, Telegrafenberg, D-14473 Potsdam, Germany ABSTRACT A detailed survey of accessory minerals in the poorly to moderately differentiated F-poor biotite granites from Niederbobritzsch, Erzgebirge, Germany, reveals the presence of various, late magmatic to postmagmatic secondary rare-earth (REE) minerals, including cerite-(Ce), thorian synchysite-(Ce), synchysite-(Ce), and an unidentified Th-rich REE fluorocarbonate(?). Cerite-(Ce) is a REE silicate that, to date, has been found in only half a dozen occurrences worldwide. It had not previously been described from a granite. The composition of cerite-(Ce) from Niederbobritzsch is characterized by lower bulk REE contents but higher abundances of Si, Al, Ca, and F than that from other occurrences. Dissolution of thorian monazite- (Ce) during interaction with a F-, CO2- and Ca-bearing fluid gave rise to the formation of thorian synchysite-(Ce) containing up to 18.1 wt% ThO2. Previously reported contents of Th in synchysite-(Ce) did not exceed 1.6 wt% ThO2. The spatial relations between the secondary REE minerals and their precursor attest to a differential mobility of the LREE and Th during fluid–rock interaction. Under the prevailing PTX-conditions, the LREE were more soluble and, thus, mobilized further away from their site of removal relative to Th, which tended to be reprecipitated next to its precursor. Virtually unchanged whole-rock REE budgets and continuous, unfractionated chondrite-normalized LREE patterns of the secondary REE minerals, however, imply that the lanthanides were transported over distances of millimeters or centimeters only. -
Mineralogy and Chemistry of Rare Earth Elements in Alkaline Ultramafic Rocks and Fluorite in the Western Kentucky Fluorspar District Warren H
University of Kentucky UKnowledge Kentucky Geological Survey Report of Kentucky Geological Survey Investigations 6-2019 Mineralogy and Chemistry of Rare Earth Elements in Alkaline Ultramafic Rocks and Fluorite in the Western Kentucky Fluorspar District Warren H. Anderson University of Kentucky, [email protected] Right click to open a feedback form in a new tab to let us know how this document benefits oy u. Follow this and additional works at: https://uknowledge.uky.edu/kgs_ri Part of the Geology Commons Repository Citation Anderson, Warren H., "Mineralogy and Chemistry of Rare Earth Elements in Alkaline Ultramafic Rocks and Fluorite in the Western Kentucky Fluorspar District" (2019). Kentucky Geological Survey Report of Investigations. 55. https://uknowledge.uky.edu/kgs_ri/55 This Report is brought to you for free and open access by the Kentucky Geological Survey at UKnowledge. It has been accepted for inclusion in Kentucky Geological Survey Report of Investigations by an authorized administrator of UKnowledge. For more information, please contact [email protected]. Mineralogy and Chemistry of Rare Earth Elements in Alkaline Ultramafic Rocks and Fluorite in the Western Kentucky Fluorspar District Warren H. Anderson Report of Investigations 8 doi.org/10.13023/kgs.ri08.13 Series XIII, 2019 Cover Photo: Various alkaline ultramafic rocks showing porphyritic, brecciated, and aphanitic textures, in contact with host limestone and altered dike texture. From left to right: • Davidson North dike, Davidson core, YH-04, 800 ft depth. Lamprophyre with calcite veins, containing abundant rutile. • Coefield area, Billiton Minner core BMN 3. Intrusive breccia with lamprophyric (al- nöite) matrix. • Maple Lake area, core ML-1, 416 ft depth. -
Stillwellite-(Ce) (Ce, La, Ca)Bsio
Stillwellite-(Ce) (Ce; La; Ca)BSiO5 c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Hexagonal. Point Group: 3: As °at rhombohedral crystals, to 4 cm, and massive. Twinning: Observed about [100]. Physical Properties: Cleavage: One imperfect. Fracture: Conchoidal. Hardness = 6.5 D(meas.) = 4.57{4.60 D(calc.) = 4.67 » Optical Properties: Transparent to translucent. Color: Red-brown to pale pink; colorless in thin section. Streak: White. Optical Class: Uniaxial (+) to biaxial (+). ! = 1.765{1.784 ² = 1.780{1.787 2V(meas.) = 0±{6± Cell Data: Space Group: P 31: a = 6.841{6.844 c = 6.700{6.702 Z = 3 X-ray Powder Pattern: Mary Kathleen mine, Australia. 3.43 (s), 2.96 (s), 2.13 (ms), 4.44 (m), 1.864 (m), 2.71 (mw), 2.24 (mw) Chemistry: (1) (2) (1) (2) (1) (2) SiO2 22.40 22.06 La2O3 27.95 19.12 MgO 0.06 UO2 0.22 Ce2O3 33.15 30.82 CaO 0.95 0.34 ThO2 5.41 Pr2O3 1.82 F 0.30 + B2O3 12.23 [13.46] Nd2O3 5.36 H2O 0.85 Al2O3 0.42 Sm2O3 0.34 H2O¡ 0.10 Y2O3 0.74 0.28 Fe2O3 0.18 P2O5 0.67 Total [100.00] [99.26] (1) Mary Kathleen mine, Australia; recalculated to 100.00% after removal of very small amounts of uraninite and apatite determined by separate analysis. (2) Vico volcano, near Vetralla, Italy; by electron microprobe, B2O3 calculated from stoichiometry, original total given as 99.23%; corresponds to (Ce0:50La0:31Nd0:08Th0:05Pr0:03Ca0:02Sm0:01)§=1:00B1:02Si0:97O5: Occurrence: Locally abundant as a metasomatic replacement of metamorphosed calcareous sediments (Mary Kathleen mine, Australia); in alkalic pegmatites in syenite in an alkalic massif (Dara-i-Pioz massif, Tajikistan). -
(Skarn)-Type Ore Deposits in Western Bergslagen,Sweden
UNIVERSITY OF GOTHENBURG Department of Earth Sciences Geovetarcentrum/Earth Science Centre PREDICTIVE PROSPECTIVITY MAPPING OF RARE EARTH ELEMENTS IN BASTNÄS (SKARN)-TYPE ORE DEPOSITS IN WESTERN BERGSLAGEN,SWEDEN INTEGRATION AND ANALYSIS OF GEOSCIENCE DATASETS IN ARCGIS Ejiro Obotuke-Agbonifo ISSN 1400-3821 B961 Master of Science (120 credits) thesis Göteborg 2017 Mailing address Address Telephone Telefax Geovetarcentrum Geovetarcentrum Geovetarcentrum 031-786 19 56 031-786 19 86 Göteborg University S 405 30 Göteborg Guldhedsgatan 5A S-405 30 Göteborg SWEDEN Table of contents 1. INTRODUCTION .................................................................................................................................... 4 1.1 AIM AND APPROACH ...................................................................................................................... 4 1.2 ABOUT RARE EARTH ELEMENTS .................................................................................................. 7 1.3 GENERAL CHARACTERISTICS OF BASTNÄS-TYPE REE MINERALIZATION ............................... 9 1.4 MINING HISTORY OF BERGSLAGEN ............................................................................................ 13 2. BACKGROUND .................................................................................................................................... 15 2.1 REGIONAL GEOLOGY OF BERGSLAGEN....................................................................................... 15 2.2 LOCAL GEOLOGY OF BERGSLAGEN ............................................................................................ -
Rare Earth Elements Deposits of the United States—A Summary of Domestic Deposits and a Global Perspective
The Principal Rare Earth Elements Deposits of the United States—A Summary of Domestic Deposits and a Global Perspective Gd Pr Ce Sm La Nd Scientific Investigations Report 2010–5220 U.S. Department of the Interior U.S. Geological Survey Cover photo: Powders of six rare earth elements oxides. Photograph by Peggy Greb, Agricultural Research Center of United States Department of Agriculture. The Principal Rare Earth Elements Deposits of the United States—A Summary of Domestic Deposits and a Global Perspective By Keith R. Long, Bradley S. Van Gosen, Nora K. Foley, and Daniel Cordier Scientific Investigations Report 2010–5220 U.S. Department of the Interior U.S. Geological Survey U.S. Department of the Interior KEN SALAZAR, Secretary U.S. Geological Survey Marcia K. McNutt, Director U.S. Geological Survey, Reston, Virginia: 2010 For product and ordering information: World Wide Web: http://www.usgs.gov/pubprod Telephone: 1-888-ASK-USGS For more information on the USGS—the Federal source for science about the Earth, its natural and living resources, natural hazards, and the environment: World Wide Web: http://www.usgs.gov Telephone: 1-888-ASK-USGS Any use of trade, product, or firm names is for descriptive purposes only and does not imply endorsement by the U.S. Government. This report has not been reviewed for stratigraphic nomenclature. 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. Suggested citation: Long, K.R., Van Gosen, B.S., Foley, N.K., and Cordier, Daniel, 2010, The principal rare earth elements deposits of the United States—A summary of domestic deposits and a global perspective: U.S. -
Ferricerite-(La) (La, Ce, Ca)9Fe (Sio4)3(Sio3oh)4(OH)3
3+ Ferricerite-(La) (La, Ce, Ca)9Fe (SiO4)3(SiO3OH)4(OH)3 Crystal Data: Hexagonal. Point Group: 3m. Forms boxwork-like aggregates of equant to tabular crystals flattened on [00*1] to 2 mm with dominant rhombohedral and pinacoidal faces, as pseudomorphs after an unidentified hexagonal prismatic mineral. Physical Properties: Cleavage: None. Tenacity: Brittle. Fracture: Conchoidal. Hardness = 5 D(meas.) = 4.7(1) D(calc.) = 4.74 Optical Properties: Translucent. Color: Light yellow to pinkish brown. Streak: White. Luster: Vitreous. Optical Class: Uniaxial (+). ω = 1.810(5) ε = 1.820(5) Cell Data: Space Group: R3c. a = 10.7493(6) c = 38.318(3) Z = 6 X-ray Powder Pattern: Mt. Yuksporr, Khibina massif, Kola Peninsula, Russia. 2.958 (100), 3.47 (40), 3.31(38), 2.833 (37), 2.689 (34), 1.949 (34), 3.53 (26) Chemistry: (1) (2) La2O3 37.57 CaO 5.09 Ce2O3 23.67 Fe2O3 1.40 Pr2O3 0.61 MgO 0.51 Nd2O3 1.48 SiO2 22.38 Sm2O3 0.10 P2O5 0.63 Gd2O3 0.24 H2O 3.20 SrO 1.97 Total 98.85 (1) Mt. Yuksporr, Khibina massif, Kola Peninsula, Russia; average electron microprobe analysis supplemented by IR spectroscopy, H2O by Penfield method; corresponds to (La4.23Ce2.65Ca1.37Sr0.35 Nd0.16Pr0.07Gd0.02Sm0.01)Σ=8.86(Fe0.32Ca0.30Mg0.23)Σ=0.85[SiO4]3[(Si0.84P0.16)Σ=1.00O3(OH)]4(OH)2.78. Mineral Group: Cerite supergroup, cerite group. Occurrence: A late-stage, low-temperature secondary phase in a symmetrically zoned, aegirine- natrolite-microcline vein in gneissose foyaite. -
Stable Isotope Systematics of Skarn-Hosted REE
Examensarbete vid Institutionen för geovetenskaper Stable Isotope Systematics of Skarn-hosted REE-silicate - ISSN 1650-6553 Nr 279 Magnetite Mineralisations in Central Bergslagen, Sweden Fredrik Sahlström Stable Isotope Systematics of The metasupracrustal-hosted, often polymetallic REE-Fe-deposits of Bastnäs- Skarn-hosted REE-silicate - type are found along the “REE-line” in the Palaeoproterozoic Bergslagen ore province, south central Sweden. They essentially comprise REE silicate- Magnetite Mineralisations in bearing magnetite skarn mineralisations with variable contents of other metals. Even though these deposits have been important for mining and research for Central Bergslagen, Sweden centuries, their origin still remains unclear. In this study, samples from 10 different deposits along the REE-line have been charactarised as to mineralogy, petrography and bulk geochemistry, in addition to their isotope systematics. Mineral separates of magnetite and, when present, co-existing quartz or carbonates have been analysed for their oxygen and (for carbonates) carbon isotope compositions, in order to put constraints on the sources for metals and fluids in these deposits. Magnetites have δ18O-values of -1.79 to 1.12 ‰, while quartzes lie between 7.19 and 8.28 ‰. Carbonates have δ18O- Fredrik Sahlström values between 5.77 and 7.15 ‰ and δ13C-values between -5.35 and -3.32 ‰. Thermometric calculations based on mineral pairs (magnetite-quartz, magnetite-calcite/dolomite), combined with available fluid inclusion data, indicate formation of primary magnetite assemblages between c. 650 to 400 °C. At these temperatures, magnetites from some of the deposits would have been in equilibrium with a magmatic fluid (δ18O = 6-8 ‰), while magnetites from other deposits would have been in equilibrium with fluids of lower δ18O (4-6 ‰). -
Technical Information: Common Tubing, Sheath, Protection Tube and Well Materials
Technical Information: Common Tubing, Sheath, Protection Tube And Well Materials Performance Characteristics Convectronics provides a variety of common tubing, selection of the proper materials for sensors used in different MgO sheath, protection tube, and drilled well materials to environments. Consult the factory for the availability of other protect temperature sensing elements from the environmental protective materials for specialty applications. NOTE: All conditions typically found in industrial process applications. chemical compositions and temperature ratings are nominal The following tables are intended as guidelines to aid in the and are stated as received from suppliers. Metals Typical Areas of Use Material/Composition MgO Prot. Drilled Application Guideline Information Tubing Sheath Tubes Wells Aluminum X Up to 1000°F (538°C) continuous. Good thermal conductivity and me- chanical strength. Oxidation can arise when not anodized or protected. Brass X X Up to 1000°F (538°C) continuous. Good thermal conductivity and mechanical strength. Carbon Steel-C1018 X X X X Up to 1000°F (538°C) in non-oxidizing environments. Main areas of us- 0.17% Carbon, 0.75% Manganese, Limited age are galvanizing pots, tinning pots, molten Babbit metal, molten Mag- 0.035 Phosphorous max., 0.045 Avail. nesium, molten Zinc, Petroleum refinery applications such as dewaxing Sulfur max., balance Iron and thermal cracking. Carpenter 20 X X X Superior resistance to stress-corrosion cracking in boiling 20-40% 34% Nickel, 20% Chromium, Limited Sulfuric Acid. Also used in high octane gas, solvents, explosives, heavy 3.5% Copper, 2.5% Molybdenum, Avail. chemicals and agrichemicals. 1.0% Silicon max., 2.0% Manganese max., .06% Carbon max., Columbian & Tantalum; 8 x C min/1 max Cast Iron X Up to 1300°F (704°C) in oxidizing conditions. -
THE REE MINERALS of the BASTNÄS-TYPE DEPOSITS, SOUTH-CENTRAL SWEDEN Volume 45 October 2007 Part 5
1073 Volume 45 October 2007 Part 5 The Canadian Mineralogist Vol. 45, pp. 1073-1114 (2007) DOI : 10.2113/gscanmin.45.5.1073 THE REE MINERALS OF THE BASTNÄS-TYPE DEPOSITS, SOUTH-CENTRAL SWEDEN DAN HOLTSTAM§ Department of Mineralogy, Swedish Museum of Natural History, Box 50007, SE–104 05 Stockholm, Sweden UL F B. ANDERSSON¶ GeoforschungsZentrum, P.B. 4.1, Telegrafenberg, D-14473 Potsdam, Germany Abstr AC T On the basis of characteristic assemblages, the Bastnäs-type Fe–(Cu–)REE skarn deposits in the Bergslagen mining region of south-central Sweden can be divided into two subtypes: one almost exclusively with LREE enrichment (subtype 1, mainly in the Riddarhyttan–Bastnäs area), and another showing enrichment of both LREE and Y + HREE (subtype 2, Norberg District). New data have been collected on twenty REE species including three unnamed ones, using electron-microprobe analysis, X-ray diffraction and Mössbauer spectroscopy. Cerite-(Ce) is, together with ferriallanite-(Ce), the most important REE mineral at Bastnäs, but less common at the subtype-2 deposits. Compared to other occurrences worldwide, the present samples of cerite-(Ce) are poor in Ca and enriched in Mg and F. Calcium and (REE + Y) in the samples are negatively correlated, and the upper limit for Ca is close to 1 apfu. Iron ranges from 0.01 to 0.30 apfu, and is mainly in the trivalent state. Cerite-(Ce) is a major carrier of Y (up to 3.5 wt.% Y2O3). Fluorbritholite is found only in the subtype-2 deposits, and is low in P, Na and the actinides compared to other major occurrences in the world. -
Orthorhombic YF3, a New Mineral from the Pitinga Mine, Presidente Figueiredo, Amazonas, Brazil and from Jabal Tawlah, Saudi Arabia: Description and Crystal Structure
Mineralogical Magazine, June 2015, Vol. 79(3), pp. 767–780 Waimirite-(Y), orthorhombic YF3, a new mineral from the Pitinga mine, Presidente Figueiredo, Amazonas, Brazil and from Jabal Tawlah, Saudi Arabia: description and crystal structure 1, 2 2 3 4 DANIEL ATENCIO *, ARTUR C. BASTOS NETO ,VITOR P. PEREIRA ,JOSE´ T. M. M. FERRON ,M.HOSHINO , 4 4 5 1 6 T. MORIYAMA ,Y.WATANABE ,R.MIYAWAKI ,JOSE´ M. V. COUTINHO ,MARCELO B. ANDRADE , 7 8 5 4 4 KENNETH DOMANIK ,NIKITA V. CHUKANOV ,K.MOMMA ,H.HIRANO AND M. TSUNEMATSU 1 Instituto de Geocieˆncias, Universidade de Sa˜o Paulo, Rua do Lago 562, 05508-080, Sa˜o Paulo, SP, Brazil 2 Instituto de Geocieˆncias, Universidade Federal do Rio Grande do Sul. Avenida Bento Gonc¸alves 9500, CEP 91501-970, Porto Alegre, RS, Brazil 3 Programa de Po´s-graduac¸a˜o em Geocieˆncias, Instituto de Geocieˆncias, Universidade Federal do Rio Grande do Sul, Brazil 4 Institute for Geo-Resources and Environment, National Institute of Advanced Industrial Science and Technology, Central 7, 1-1-1 Higashi, Tsukuba, Ibaraki 305-8567, Japan 5 Department of Geology and Paleontology, National Museum of Nature and Science, 4-1-1 Amakubo, Tsukuba, Ibaraki 305-0005, Japan 6 Sa˜o Carlos Institute of Physics, University of Sa˜o Paulo, Caixa Postal 369, 13560-970, Sa˜o Carlos, SP, Brazil 7 Lunar and Planetary Laboratory, University of Arizona, 1629 E. University Blvd., Tucson, AZ, 85721-0092, USA 8 Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow region, 142432 Russia [Received 12 August 2014; Accepted 8 January 2015; Associate Editor: D. -
Exemption for the Use of Cadmium in Portable Batteries and Accumulators
Exemption for the use of cadmium in portable batteries and accumulators intended for the use in cordless power tools in the context of the Batteries Directive 2006/66/EC Final Report (revised) 26 January 2010 Consortium ESWI Expert TeamBIPRO, to S upportUmweltbundesamt Waste Implementation BiPRO Beratungsgesellschaft für integrierte Problemlösungen ENV.G.4/FRA/2007/0066 iii European Commission ESWI Final Report - Replacement of Cadmium Batteries in Cordless Power Tools ENV.G.4/FRA/2007/0066 iv Executive Summary Background The Batteries Directive 2006/66/EC (repealing Directive 91/157/EEC) entered into force on 26 September 20061. The Directive sets out rules applicable to all batteries and accumulators that are put on the European Union market. These rules include, among others, restriction on the use of cadmium in portable batteries and accumulators (PBA) according to Article 4(1)(b) of the Directive. Portable batteries and accumulators, including those incorporated into appliances, that contain more than 0,002% of cadmium by weight shall not be placed on the market. However, according to Article 4(3) of the Directive the above requirement shall not apply to portable batteries and accumulators intended for use in: (a) emergency and alarm systems, including emergency lighting; (b) medical equipment; or (c) cordless power tools. Furthermore, based on Article 4(4) of the Directive the Commission shall review the exemption from the cadmium ban for use in cordless power tool with a view to the prohibition of cadmium in batteries and accumulators. The Commission shall submit a corresponding report to the European Parliament and to the Council by 26 September 2010, together, if appropriate, with relevant proposals. -
Aluminocerite-Ce: a New Species from Baveno, Italy: Description and Crystal-Structure Determination
American Mineralogist, Volume 94, pages 487–493, 2009 Aluminocerite-Ce: A new species from Baveno, Italy: Description and crystal-structure determination FABRIZIO NESTOLA ,1,* ALESSA N DRO GUASTO N I ,1 FER N A N DO CÁMARA ,2 LU C IA N O SE cc O ,1 ALBERTO DAL NE G RO ,1 DA N ILO PEDRO N ,3 A N D AN TO N BERA N 4 1Dipartimento di Geoscienze, Università di Padova, Via Giotto 1, 35137, Padova, Italy 2C.N.R., Istituto di Geoscienze e Georisorse, Unità di Pavia, Via Ferrata 1, 27100 Pavia, Italy 3Dipartimento di Scienze Chimiche, Università di Padova, Via Marzolo 1, 35131, Padova, Italy 4Institute of Mineralogy and Crystallography, University of Vienna, Althanstrasse 14, 1090 Vienna, Austria ABSTRA C T Aluminocerite-(Ce), ideally (Ce,Ca)9Al(SiO4)3[SiO3(OH)]4(OH)3, is isostructural with cerite-(Ce) and cerite-(La). The holotype was found at the Ratti quarry, near Baveno, Italy, in millimeter-sized secondary cavities hosted in aplite-pegmatite veins and pods within pink granite. Aluminocerite-(Ce) forms aggregates of pseudo-octahedral to rhombohedral crystals flattened on the c axis. The cotype of aluminocerite-(Ce) was discovered at the Locatelly quarry, also near Baveno, where it occurs in centimeter-sized miarolitic cavities in pink granite. The mineral is pale pink to pink-reddish, with a white streak, and is translucent with a vitreous luster. Aluminocerite-(Ce) is non-fluorescent. The hardness based on the Mohs scale is 5, and the tenacity is brittle. Neither cleavage, fracture, or twinning were 3 observed. Calculated density is 4.675 g/cm .