Titanian Taramellites in Western North America
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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 -
Crystal Structure of Bage [Ge3 O9] and Its Relation to Benitoite
------------- ., JOURNAL OF RESEARCH of the National Bureau of Standards - A. Physics and Chemistry Vol. 70A, No.5, September-October 1966 Crystal Structure of BaGe [ Ge3 0 9 Jand Its Relation to Benitoite I I C. Robbins, A. Perloff, and S. Block ~ ( Institute for Materials Research, National Bureau of Standards, Washington, D.C. 20234 I (May 23, 1966) BaGe[Ge30gl is trigonal, space group P3, with lattice constants a= 11.61, c=4.74 A, and Z =3. The structure was established by three·dimensional Patterson and electron density syntheses. Three·dimensional least·squares refinement resulted in a final R value of 6.8 percent (observed data only). The previously proposed structural relationship of this compound with benitoite, BaTiSbOg, has been confirmed. The structure can be considered as composed of Ge30g rings, in which the Ge is tetrahedrally coordinated, linked through octahedrally coordinated Ge atoms to form a three·dimen· sional Ge·O network. All Ge polyhedra are linked by corner sharing. The Ba ions occupy positions in channels of the network. Key Words: Barium tetragermanate, structure, benitoite, crystal, x·ray. 1. Introduction Robbins and Levin [lJ. Their data plus the space group information are: The synthesis of three germanates of formula type MeGe4 0g (Me = Sr, Pb, Ba) was reported by Robbins a=lL61 A w= L797±0.003 and Levin [lJ .1 A comparison of indexed powder c=4.74A E= 1.783 ± 0.003 patterns suggested that the compounds were isostruc S.G.=P3 p (obs) = 5.1 gcm - 3 turaL This was later confirmed by Eulenberger, Z =3 p (calc) = 5.12 gcm- 3 Wittman, and Nowotny [2]. -
List of New Mineral Names: with an Index of Authors
415 A (fifth) list of new mineral names: with an index of authors. 1 By L. J. S~v.scs~, M.A., F.G.S. Assistant in the ~Iineral Department of the,Brltish Museum. [Communicated June 7, 1910.] Aglaurito. R. Handmann, 1907. Zeita. Min. Geol. Stuttgart, col. i, p. 78. Orthoc]ase-felspar with a fine blue reflection forming a constituent of quartz-porphyry (Aglauritporphyr) from Teplitz, Bohemia. Named from ~,Xavpo~ ---- ~Xa&, bright. Alaito. K. A. ~Yenadkevi~, 1909. BuU. Acad. Sci. Saint-P6tersbourg, ser. 6, col. iii, p. 185 (A~am~s). Hydrate~l vanadic oxide, V205. H~O, forming blood=red, mossy growths with silky lustre. Founi] with turanite (q. v.) in thct neighbourhood of the Alai Mountains, Russian Central Asia. Alamosite. C. Palaehe and H. E. Merwin, 1909. Amer. Journ. Sci., ser. 4, col. xxvii, p. 899; Zeits. Kryst. Min., col. xlvi, p. 518. Lead recta-silicate, PbSiOs, occurring as snow-white, radially fibrous masses. Crystals are monoclinic, though apparently not isom0rphous with wol]astonite. From Alamos, Sonora, Mexico. Prepared artificially by S. Hilpert and P. Weiller, Ber. Deutsch. Chem. Ges., 1909, col. xlii, p. 2969. Aloisiite. L. Colomba, 1908. Rend. B. Accad. Lincei, Roma, set. 5, col. xvii, sere. 2, p. 233. A hydrated sub-silicate of calcium, ferrous iron, magnesium, sodium, and hydrogen, (R pp, R',), SiO,, occurring in an amorphous condition, intimately mixed with oalcinm carbonate, in a palagonite-tuff at Fort Portal, Uganda. Named in honour of H.R.H. Prince Luigi Amedeo of Savoy, Duke of Abruzzi. Aloisius or Aloysius is a Latin form of Luigi or I~ewis. -
Reflective Index Reference Chart
REFLECTIVE INDEX REFERENCE CHART FOR PRESIDIUM DUO TESTER (PDT) Reflective Index Refractive Reflective Index Refractive Reflective Index Refractive Gemstone on PDT/PRM Index Gemstone on PDT/PRM Index Gemstone on PDT/PRM Index Fluorite 16 - 18 1.434 - 1.434 Emerald 26 - 29 1.580 - 1.580 Corundum 34 - 43 1.762 - 1.770 Opal 17 - 19 1.450 - 1.450 Verdite 26 - 29 1.580 - 1.580 Idocrase 35 - 39 1.713 - 1.718 ? Glass 17 - 54 1.440 - 1.900 Brazilianite 27 - 32 1.602 - 1.621 Spinel 36 - 39 1.718 - 1.718 How does your Presidium tester Plastic 18 - 38 1.460 - 1.700 Rhodochrosite 27 - 48 1.597 - 1.817 TL Grossularite Garnet 36 - 40 1.720 - 1.720 Sodalite 19 - 21 1.483 - 1.483 Actinolite 28 - 33 1.614 - 1.642 Kyanite 36 - 41 1.716 - 1.731 work to get R.I. values? Lapis-lazuli 20 - 23 1.500 - 1.500 Nephrite 28 - 33 1.606 - 1.632 Rhodonite 37 - 41 1.730 - 1.740 Reflective indices developed by Presidium can Moldavite 20 - 23 1.500 - 1.500 Turquoise 28 - 34 1.610 - 1.650 TP Grossularite Garnet (Hessonite) 37 - 41 1.740 - 1.740 be matched in this table to the corresponding Obsidian 20 - 23 1.500 - 1.500 Topaz (Blue, White) 29 - 32 1.619 - 1.627 Chrysoberyl (Alexandrite) 38 - 42 1.746 - 1.755 common Refractive Index values to get the Calcite 20 - 35 1.486 - 1.658 Danburite 29 - 33 1.630 - 1.636 Pyrope Garnet 38 - 42 1.746 - 1.746 R.I value of the gemstone. -
PABSTITE from the DARA-I-PIOZ MORAINE (TADJIKISTAN)
New data on minerals. M.: 2003. Volume 38 UDC 549.6 PABSTITE FROM THE DARA-i-PIOZ MORAINE (TADJIKISTAN) Leonid A. Pautov Fersman Mineralogical Museum of the Russian Academy of Science. Moscow, [email protected] Pabstite was discovered in the moraine of the Dara-i-Pioz glacier (Garmsky district, Tadjikistan) in a leuco- cratic rock mainly composed of microcline, quartz, and albite. Subordinated minerals are aegirine, titanite, astrophyllite, bafertisite, galena, sphalerite, ilmenite, pyrochlore, fluorite, zircon, fluorapatite, and calcite. Pabstite forms grains and well-faced crystals (0.1-0.5 mm), growing on quartz crystals in small cavities abun- dant in the rock. Its composition is close to the final member BaSnSi:P9 in the series pabstite-benitoite. Microprobe analysis has shown: SiO, - 37.43; Ti02 - 0.19; Zr02 - 0.16; Sn02 - 30.05; BaO - 32.41; total 100.24. The empirical formula is Balo2(Sno96Tio.01Zroo,)o98Si3o,09'Refraction parameters of pabstite are no = 1.668(2); 1.657(2), which is much lower than cited figures for pabstite from the type locality. Strong n" = dependence of pabstite optical properties on titanium contents is shown. The find of pabstite at Dara-i-Pioze is the first find of pabstite in alkaline rocks and, apparently, the second find of this mineral in the world. 2 tables, 3 figures and 13 references. Pabstite BaSnSi30g, the tin analogue of beni- aegirine syenites and foyaites. The first data on toite, was described as a new mineral from the massif were received at works of Tadjik- Santa Cruz (California, USA), where it was met Pamirs expedition of 1932 - 1936. -
RARE EARTHS in MINERALS of the JOAQUINITE GROUP E. I. Sblrbnov,Lv
THE AMERICAN MINERALOGIST, VOL. 52, NOVEMBER-DECEMBER, 1967 RARE EARTHS IN MINERALS OF THE JOAQUINITE GROUP E. I. SBlrBNov,lV. f. Buxrw,2YU. A. Ber.Asuov,2aNr H. SdnnNsBuB ABsrRAcr An apparently new rare-earth mineral of the joaquinite group occurs in nephelin-syenite pegmatites of Ilimaussaq alkaline massif (S. Greenland). Optical and X-ray properties are the same, as for standard joaquinite NaBaTirSirOrs from California, but the chemical analysis is quite difierent: SiO, 33.82, NbzOs 2.31, TiO29.20, Feror 0.39, FeO 4.78, MnO 0.70, ThOz 0.38, RErOs 22.59, BaO 21.46, (Ca, Sr)O 0.03, Na:O 2.41, KzO 0.22, HzO 1.50, F 0 38, -O:F2-0.16, sum 100.01.The formula is NaBa2Fe2+CezTi:SisOr6(OH)(Z:4). Semiquantitative analyses of California joaquinite also showed the presence of consider- able rare earths. INrnooucrroN During summer field work (1964) in the expedition of the Greenland Geological Survey, headed by H. Sfrensen, in the Ilimaussaq alkaline massif (S. Greenland), E. L Semenov found an unknown mineral of composition NaBarFeCezTi2Si8O26(OH)containing 2370 F.E1o3in the nepheline syenite pegmatites. At present no barium-titanium silicate minerals containing rare earths are known. However, the Soviet Com- mission on New Minerals observed the similarity of unit cell dimensions and optical affinities of this mineral with joaquinite, NaBa(Ti,Fe)aSiaOrr,, for which the content of rare earths was not shown in analyses.Therefore both minerals were studied. Joaquinite has been described from San Benito County, California (Palacheand Foshag,1932), and from SealLake, Quebec,Canada (Bell, 1963).One California specimen(No. -
(Sr,Ca)2Ba3(PO4)3F, a New Mineral of the Hedyphane Group in the Apatite Supergroup from the Shimoharai Mine, Oita Prefecture, Japan
Journal of MineralogicalMiyahisaite, and Petrological a new mineral Sciences, of the hedyphane Volume 107, group page 121─ 126, 2012 121 Miyahisaite, (Sr,Ca)2Ba3(PO4)3F, a new mineral of the hedyphane group in the apatite supergroup from the Shimoharai mine, Oita Prefecture, Japan * ** ** Daisuke NISHIO-HAMANE , Yukikazu OGOSHI and Tetsuo MINAKAWA * The Institute for Solid State Physics, the University of Tokyo, Kashiwa 277-8581, Japan **Departments of Earth Science, Faculty of Science, Ehime University, Matsuyama 790-8577, Japan Miyahisaite, (Sr,Ca)2Ba3(PO4)3F, a new mineral of the hedyphane group in the apatite supergroup, is found in the Shimoharai mine, Oita Prefecture, Japan. Miyahisaite is colorless and occurs as a pseudomorphic aggregate (up to about 100 μm in size) along with fluorapatite in the quartz matrix in a namansilite-rich layer of the chert. Its hardness is 5 on the Mohs scale, and its calculated density is 4.511 g/cm3. The empirical formula of miyahi- saite is (Sr1.366Ca0.717)Σ2.083Ba2.911P3.002O12(F0.898OH0.088Cl0.014)Σ1.00, which is representatively shown as (Sr,Ca)2 Ba3(PO4)3F. Its simplified ideal formula is written as Sr2Ba3(PO4)3F, which requires 23.25 wt% SrO, 51.62 wt% BaO, 23.89 wt% P2O5, 2.13 wt% F, and −0.90 wt% F = O, for a total of 100.00 wt%. The mineral is hexagonal 3 with a space group P63/m, unit cell parameters a = 9.921 (2) Å, c = 7.469 (3) Å, and V = 636.7 (3) Å , and Z = 2. The eight strongest lines in the powder XRD pattern [d (Å), (I/I0), hkl] are 3.427 (16) 102, 3.248 (22) 120, 2.981 (100) 121, 2.865 (21) 300, 1.976 (23) 123, 1.874 (16) 140, 1.870 (15) 004, and 1.864 (17) 402. -
29 Devitoite, a New Heterophyllosilicate
29 The Canadian Mineralogist Vol. 48, pp. 29-40 (2010) DOl: 1O.3749/canmin.48.1.29 DEVITOITE, A NEW HETEROPHYLLOSILICATE MINERAL WITH ASTROPHYLLITE-LiKE LAYERS FROM EASTERN FRESNO COUNTY, CALIFORNIA ANTHONY R. KAMPP§ Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, California 90007, USA. GEORGE R. ROSSMAN Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California 91125-2500, USA. IAN M. STEELE AND JOSEPH J. PLUTH Department of the Geophysical Sciences, The University of Chicago, 5734 S. Ellis Avenue, Chicago, Illinois 60637, U.S.A. GAIL E. DUNNING 773 Durshire Way, Sunnyvale, California 94087, U.S.A. ROBERT E. WALSTROM P. O. Box 1978, Silver City, New Mexico 88062, USA. ABSTRACT Devitoite, [Ba6(P04MC03)] [Fe2+7Fe3+2(Si4012h02(OH)4], is a new mineral species from the Esquire #8 claim along Big Creek in eastern Fresno County, California, U.SA. It is also found at the nearby Esquire #7 claim and at Trumbull Peak in Mariposa County. The mineral is named for Alfred (Fred) DeVito (1937-2004). Devitoite crystallized very late in a sequence of minerals resulting from fluids interacting with a quartz-sanbornite vein along its margin with the country rock. The mineral occurs in subparallel intergrowths of very thin brown blades, flattened on {001} and elongate and striated parallel to [100]. The mineral has a cream to pale brown streak, a silky luster, a Mohs hardness of approximately 4, and two cleavages: {OO!} perfect and {01O} good. The calculated density is 4.044 g/cm '. It is optically biaxial (+), Cl 1.730(3), 13 1.735(6), 'Y 1.755(3); 2Vcalc = 53.6°; orientation: X = b, Y = c, Z = a; pleochroism: brown, Y»> X> Z. -
Alforsite, a New Member of the Apatite Group: the Barium Analogue of Chlorapatite1
American Mineralogist, Volume 66, pages 1050-1053, 1981 Alforsite, a new member of the apatite group: the barium analogue of chlorapatite1 NANCY G. NEWBERRY, ERIC J. ESSENE, AND DONALD R. PEACOR Department of Geological Sciences University of Michigan Ann Arbor, Michigan 48109 Abstract Alforsite, ideally Ba,(P04)3Cl, is a new member of the apatite group occurring in contact m.etamorphosed evaporitic rocks from Fresno and Mariposa counties, California, associated wlth fluor~patit: and m~ny. other rare barium minerals previously described by Alfors et al. (1965). It IS optically umaxlal, negative, with W,E= 1.70(1). The density is calculated to be 4.83(2) gm/cm3 for the end member composition. It is hexagonal, space group P63/m, with a = 10.25(1) and c = 7.64(2)A. The strongest lines in the powder pattern are 3.06(100), 2.95(30), 2.1~(30), 2.03(30), and 1.928(30). The associated assemblage of witherite, quartz, and s~~ornlte buffers the C02 fugacity at metamorphic pressures and temperatures. The name 1.s.mhono~ of Dr: Jo~ T. Alfors of the California Division of Mines and Geology in recogmtlOn of hlS contnbutlOns to the study of barium minerals. Introduction study. The phase was found to have the structural The sanbornite deposits of eastern Fresno and and physical characteristics of apatite, and deter- Mariposa counties, California, contain many rare mined to be the barium analogue of chlorapatite. As barium minerals, principally silicates (Rogers, 1932). the natural phase is rare and very fine-grained even The metamorphic sanbornite-quartz rock and fo- at the type locality, studies were supplemented by liated quartzite, both of which contain the new min- work on a synthetic end-member barium chlorapatite eral, are described by Matthews and Alfors (1962), supplied by Dr. -
Mineralogy and Crystal Structures of Barium Silicate Minerals
MINERALOGY AND CRYSTAL STRUCTURES OF BARIUM SILICATE MINERALS FROM FRESNO COUNTY, CALIFORNIA by LAUREL CHRISTINE BASCIANO B.Sc. Honours, SSP (Geology), Queen's University, 1998 A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE in THE FACULTY OF GRADUATE STUDIES (Department of Earth and Ocean Sciences) We accept this thesis as conforming to the required standard THE UNIVERSITY OF BRITISH COLUMBIA December 1999 © Laurel Christine Basciano, 1999 In presenting this thesis in partial fulfilment of the requirements for an advanced degree at the University of British Columbia, I agree that the Library shall make it freely available for reference and study. I further agree that permission for extensive copying of this thesis for scholarly purposes may be granted by the head of my department or by his or her representatives. It is understood that copying or publication of this thesis for financial gain shall not be allowed without my written permission. Department of !PcX,rU\ a^/icJ OreO-^ Scf&PW The University of British Columbia Vancouver, Canada Date OeC S/79 DE-6 (2/88) Abstract The sanbornite deposits at Big Creek and Rush Creek, Fresno County, California are host to many rare barium silicates, including bigcreekite, UK6, walstromite and verplanckite. As part of this study I described the physical properties and solved the crystal structures of bigcreekite and UK6. In addition, I refined the crystal structures of walstromite and verplanckite. Bigcreekite, ideally BaSi205-4H20, is a newly identified mineral species that occurs along very thin transverse fractures in fairly well laminated quartz-rich sanbornite portions of the rock. -
STRONG and WEAK INTERLAYER INTERACTIONS of TWO-DIMENSIONAL MATERIALS and THEIR ASSEMBLIES Tyler William Farnsworth a Dissertati
STRONG AND WEAK INTERLAYER INTERACTIONS OF TWO-DIMENSIONAL MATERIALS AND THEIR ASSEMBLIES Tyler William Farnsworth A dissertation submitted to the faculty at the University of North Carolina at Chapel Hill in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Department of Chemistry. Chapel Hill 2018 Approved by: Scott C. Warren James F. Cahoon Wei You Joanna M. Atkin Matthew K. Brennaman © 2018 Tyler William Farnsworth ALL RIGHTS RESERVED ii ABSTRACT Tyler William Farnsworth: Strong and weak interlayer interactions of two-dimensional materials and their assemblies (Under the direction of Scott C. Warren) The ability to control the properties of a macroscopic material through systematic modification of its component parts is a central theme in materials science. This concept is exemplified by the assembly of quantum dots into 3D solids, but the application of similar design principles to other quantum-confined systems, namely 2D materials, remains largely unexplored. Here I demonstrate that solution-processed 2D semiconductors retain their quantum-confined properties even when assembled into electrically conductive, thick films. Structural investigations show how this behavior is caused by turbostratic disorder and interlayer adsorbates, which weaken interlayer interactions and allow access to a quantum- confined but electronically coupled state. I generalize these findings to use a variety of 2D building blocks to create electrically conductive 3D solids with virtually any band gap. I next introduce a strategy for discovering new 2D materials. Previous efforts to identify novel 2D materials were limited to van der Waals layered materials, but I demonstrate that layered crystals with strong interlayer interactions can be exfoliated into few-layer or monolayer materials. -
STRONTIUM-APATITE: NEW OCCURRENCES, and the EXTENT of Sr-FOR-Ca SUBSTITUTION in APATITE-GROUP MINERALS
121 The Canadian Mineralogist Vol. 40, pp. 121-136 (2002) STRONTIUM-APATITE: NEW OCCURRENCES, AND THE EXTENT OF Sr-FOR-Ca SUBSTITUTION IN APATITE-GROUP MINERALS ANTON R. CHAKHMOURADIAN§ Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada EKATERINA P. REGUIR and ROGER H. MITCHELL Department of Geology, Lakehead University, Thunder Bay, Ontario P7B 5E1, Canada ABSTRACT The paragenesis and compositional variation of strontium-apatite from three new localities are characterized. At Lovozero, in the Kola Peninsula, Russia, strontium-apatite forms elongate crystals and thin reaction-induced rims on early strontian fluorapatite in nepheline syenite pegmatites. The apatite-group minerals are enriched in Na and REE, and exhibit the following compositional range: (Ca0.34–4.49Sr0.18–4.54Na0.05–0.30REE0.08–0.18Ba0–0.10)(P2.87–3.03Si0–0.16)O12(F,OH). At Murun, in eastern Siberia, Russia, strontium-apatite also occurs in intimate association with strontian fluorapatite in a eudialyte-bearing nepheline syenite pegmatite. The overall compositional variation of these minerals can be expressed as (Ca2.26–3.55Sr1.41–2.74Na0–0.03REE0–0..08)(P2.91–3.01Si0– 0.06)O12(F,OH). At Lac de Gras, Northwest Territories, Canada, strontium-apatite and Sr-rich carbonate-hydroxylapatite compose cores of spherulites confined to vesicles in kimberlite, associated with suolunite and barian phlogopite. In addition to Sr, the apatite is enriched in Ba and V; the proportions of these elements decrease from the center of spherulites outward. The Lac de Gras apatite is inferred to contain carbon substituting for P. The overall compositional variation is (Sr0.08–2.58Ca2.04–4.65Ba0– 0.21Na0.09–0.28REE0–0.07K0–0.03)(P2.20–2.61C~0.25–0.50Si0.04–0.26V0–0.13)O12(OH,F).