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Washington State Minerals Checklist
Division of Geology and Earth Resources MS 47007; Olympia, WA 98504-7007 Washington State 360-902-1450; 360-902-1785 fax E-mail: [email protected] Website: http://www.dnr.wa.gov/geology Minerals Checklist Note: Mineral names in parentheses are the preferred species names. Compiled by Raymond Lasmanis o Acanthite o Arsenopalladinite o Bustamite o Clinohumite o Enstatite o Harmotome o Actinolite o Arsenopyrite o Bytownite o Clinoptilolite o Epidesmine (Stilbite) o Hastingsite o Adularia o Arsenosulvanite (Plagioclase) o Clinozoisite o Epidote o Hausmannite (Orthoclase) o Arsenpolybasite o Cairngorm (Quartz) o Cobaltite o Epistilbite o Hedenbergite o Aegirine o Astrophyllite o Calamine o Cochromite o Epsomite o Hedleyite o Aenigmatite o Atacamite (Hemimorphite) o Coffinite o Erionite o Hematite o Aeschynite o Atokite o Calaverite o Columbite o Erythrite o Hemimorphite o Agardite-Y o Augite o Calciohilairite (Ferrocolumbite) o Euchroite o Hercynite o Agate (Quartz) o Aurostibite o Calcite, see also o Conichalcite o Euxenite o Hessite o Aguilarite o Austinite Manganocalcite o Connellite o Euxenite-Y o Heulandite o Aktashite o Onyx o Copiapite o o Autunite o Fairchildite Hexahydrite o Alabandite o Caledonite o Copper o o Awaruite o Famatinite Hibschite o Albite o Cancrinite o Copper-zinc o o Axinite group o Fayalite Hillebrandite o Algodonite o Carnelian (Quartz) o Coquandite o o Azurite o Feldspar group Hisingerite o Allanite o Cassiterite o Cordierite o o Barite o Ferberite Hongshiite o Allanite-Ce o Catapleiite o Corrensite o o Bastnäsite -
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 -
The Crystal Structure of Boleit+A Mineral Containing Silver Atom Clusters
JOURNAL OF SOLID STATE CHEMISTRY 6,86-92 (1973) The Crystal Structure of Boleit+A Mineral Containing Silver Atom Clusters ROLAND C. ROUSE Department of Geology and Mineralogy,* The University of Michigan, Ann Arbor, Michigan 48104 Received March IO,1972 The mineral boleite, Pb26Ag,Cu~,CI,1(OH)1s, is cubic, space group Pm3m, with u = 15.29 A. Lead and silver atoms form a distorted body-centered array leading to octahedral groupings of these atoms. The silver atoms and their coordinating chlorines form Ag&18C16 groups similar to those in the metal cluster compounds MoCI, and WCL. Lead and conoer atoms are in distorted square antiprismatic and tetragonal bipyramidal coordination, r&ectively. - - Introduction gradually from blue to green, while the bire- Boleite is a lead copper oxychloride mineral fringent rim and the quasi-isotropic core merged which occurs as deep blue crystals of cubic form. into an apparently homogeneous, isotropic These cubes are zoned and consist of an optically phase. Upon cooling, the blue color returned but isotropic or quasi-isotropic core and a bire- the isotropy persisted. From these and other fringent outer rim of complex structure. The cube observations Winchell proposed that boleite faces are sometimes occupied by epitaxial undergoes an inversion from a pseudocubic form overgrowths of the related speciespseudoboleite to a cubic one with increasing temperature. and cumengite. Boleite has been studied in detail by Mallard and Cumenge (I), Friedel (2), and Symmetry and Composition Hocart (3). They all considered the birefringent To determine the true symmetry of boleite, material to be tetragonal and untwinned and the isotropic cleavage fragments were examined by isotropic core to be pseudocubic due to twinning. -
Pseudoboleite Pb31cu24cl62(OH)48 C 2001-2005 Mineral Data Publishing, Version 1
Pseudoboleite Pb31Cu24Cl62(OH)48 c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Tetragonal, pseudocubic. Point Group: 4/m 2/m 2/m. Very rarely as single crystals, to 1 mm; commonly intergrown with and overgrown on boleite with mutually k{001}. Physical Properties: Cleavage: {001}, perfect; {101}, nearly perfect. Hardness = 2.5 D(meas.) = 4.85 D(calc.) = 5.07 Optical Properties: Translucent. Color: Indigo blue. Luster: Pearly on cleavages. Optical Class: Uniaxial (–). ω = 2.03 = 2.00 Cell Data: Space Group: I4/mmm. a = 15.24(2) c = 30.74(5) Z = 2 X-ray Powder Pattern: Chancay, Peru; may totally obscure the pattern of intergrown boleite. (ICDD 22-470). 4.43 (100), 3.83 (100), 2.707 (95), 2.334 (65), 2.551 (60), 2.389 (60), 1.990 (60) Chemistry: (1) (2) (3) AgCl 1.6 Pb 53.5 57.7 56.37 CuO 16.5 16.9 16.75 Cl 20.2 19.8 19.29 H2O 5.5 5.6 7.59 insol. 0.8 Total 98.1 [100.0] 100.00 (1) Boleo, Mexico. (2) Analysis (1) corrected to 100.0% after deduction of AgCl 1.6% as boleite and insoluble 0.8%. (3) Pb31Cu24Cl62(OH)48. Occurrence: A secondary mineral formed through reaction of chloride with primary sulfides in the oxidized zone of Pb–Cu deposits; in smelter slag immersed in and leached by sea water. Association: Boleite, cumengeite, atacamite, anglesite, cerussite, phosgenite, gypsum (Boleo, Mexico). Distribution: In Mexico, in the Amelia mine, Boleo, near Santa Rosal´ıa,Baja California, and from an undefined locality in Sonora. -
BOLEITE: RESOLUTION of the FORMULA, K Pb26 Ag9 Cu24 Cl62 (OH)48
801 The Canadian Mineralogist Vol. 38, pp. 801-808 (2000) BOLEITE: RESOLUTION OF THE FORMULA, K Pb26 Ag9 Cu24 Cl62 (OH)48 MARK A. COOPER AND FRANK C. HAWTHORNE§ Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada ABSTRACT 3 The crystal structure of boleite, K Pb26 Ag9 Cu24 Cl62 (OH)48, a 15.288(2) Å, V 3574(1) Å , Pm 3¯ m, Z = 1, has been refined to an R-index of 2.2% based on 884 observed (5) reflections collected with MoK␣ X-radiation. A new site was resolved, and site-scattering refinement showed it to be occupied by a scattering species with 19 epfu (electrons per formula unit); this result is in accord with complete occupancy of this site by K. Potassium was detected by electron-microprobe analysis, but the amount determined is only ~50% of the amount indicated by site-scattering refinement. However, the refinement results show K to be disordered within a large cage in the structure, and the electron-beam bombardment probably induces rapid migration of K within the structure. Infrared spectroscopy shows that there is no H2O present in the structure. The H-sites were determined during refinement, and a sensible H-bonding scheme results. Keywords: boleite, crystal structure, new formula, hydrogen bonding. SOMMAIRE 3 Nous avons affiné la structure cristalline de la boléite, K Pb26 Ag9 Cu24 Cl62 (OH)48, a 15.288(2) Å, V 3574(1) Å , Pm¯3m, Z = 1, jusqu’à un résidu R de 2.2% en utilisant 884 réflexions observées (5) prélevées avec rayonnement MoK␣. -
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). -
Diamond Dan's Mineral Names Dictionary
A Dictionary of Mineral Names By Darryl Powell Mineral Names What do they mean? Who created them? What can I learn from them? This mineral diction‐ ary is unique because it is illustrated, both with mineral drawings as well as pictures of people and places after which some minerals are named. The people pictured on this page have all made a con‐ tribution to what is formally called “mineral nomenclature.” Keep reading and you will discover who they are and what they did. In 1995, Diamond Dan Publications pub‐ lished its first full book, “A Mineral Collector’s Guide to Common Mineral Names: Their Ori‐ gins & Meanings.” Now it is twenty years later. What you will discover in this issue and in the March issue is a re‐ vised and improved version of this book. This Mineral Names Dictionary contains mineral names that the average mineral collector will encounter while collecting minerals, attending shows and visiting museum displays. In addition to the most common min‐ eral names, there are some unofficial names which you will still find on labels. Each mineral name has a story to tell or a lesson to teach. If you wanted to take the time, each name could become a topic to study. Armalcolite, for example, could quickly be‐ come a study of a mineral, first discovered on the moon, and brought back to earth by the astronauts Armstrong, Aldrin and Collins (do you see parts of their names in this mineral name?) This could lead you to a study of American astronauts landing on the moon, what it took to get there and what we discovered by landing on the moon. -
Chapter 4 Phytomorph and Geomorph Identification ©
1 Chapter 4 Phytomorph and Geomorph Identification © This Chapter is based on three published works: (1) a paper by Hugh O Neall (1944) that identifies two New World plants (sunflower and chili peppers) in the Voynich manuscript; (2) a paper of Tucker and Talbert (2013) which identified 39 plants in the Voynich as indigenous to the New World; (3) a paper by Tucker and Janick (2016) which extended the list to 59 species. Although many of the illustrations of the Voynich Codex on first blush could be considered bizarre or whimsical (See Figure in Chapter 14) most contain morphological structures which permit botanical identification. Many enthusiasts have attempted to analyze the plants of the Voynich Codex, but few are knowledgeable plant taxonomists or botanists, despite their large web presence. Most of the plant identification has been predicated on the conclusion that the Voynich is a 15th century European manuscript (Friedman 1962). The principal reports in a web report by non botanists Edith and Erica Sherwood (http:www.edithsherwood.comn/coyhnich_botanical_plants) who identifies he plants as Mediterranean based on their premise that Voynich is a 15th century Italian manuscript and claims to find signature of Leonardo da Vinci in voynich drawings. We respectfully disagree with both assertions. The first exception to the conclusion that the Voynich plants were European is a short remarkable 1944 paper in Speculum (a refereed journal of the Medieval Academy of America) by the distinguished plant taxonomist, the Rev./Dr. Hugh O’Neill (1894–1969), former Director of the Herbarium (official acronym LCU) at the Catholic University of America (CUA) in Washington, D.C. -
Matlockite Pbfcl C 2001-2005 Mineral Data Publishing, Version 1
Matlockite PbFCl c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Tetragonal. Point Group: 4/m 2/m 2/m. Tabular crystals, to 5 cm, flattened on {001}, with {110}, {011}, and {111} modifications, may be equant, rounded. In subparallel aggregates, rosettelike, radiating, hemispherical; lamellar, cleavable massive. Physical Properties: Cleavage: {001}, perfect. Fracture: Uneven to subconchoidal. Tenacity: Brittle. Hardness = 2.5–3 D(meas.) = 7.12 D(calc.) = 7.16 Optical Properties: Transparent. Color: Colorless, pale yellow, amber-yellow, yellow-orange; colorless in transmitted light. Luster: Adamantine, pearly on {001}. Optical Class: Uniaxial (–); rarely biaxial due to strain. ω = 2.145 = 2.006 2V(meas.) = Small. Cell Data: Space Group: P 4/nmm (synthetic). a = 4.1104(2) c = 7.2325(5) Z = 2 X-ray Powder Pattern: Synthetic. 3.574 (100), 2.906 (45), 3.617 (40), 2.265 (40), 2.715 (35), 1.781 (25), 2.055 (20) Chemistry: (1) (2) (3) Pb 79.55 78.92 79.19 F 7.11 7.25 7.26 Cl 13.44 13.57 13.55 Total 100.10 [99.74] 100.00 (1) Cromford, England. (2) Tiger, Arizona, USA; original total given as 99.67%. (3) PbFCl. Occurrence: In the oxide zone of some lead-bearing mineral deposits. Association: Phosgenite, anglesite, cerussite, galena, sphalerite, barite, fluorite (Cromford, England); diaboleite, boleite, caledonite, leadhillite (Tiger, Arizona, USA). Distribution: Large crystals from the Bage and Wallclose mines, about 2.5 km south of Matlock, Derbyshire, England. In slag, at Laurium, Greece. In slag, along Baratti Beach and one km north of Campiglia, Tuscany, Italy. -
Minerals of Arizona Report
MINERALS OF ARIZONA by Frederic W. Galbraith and Daniel J. Brennan THE ARIZONA BUREAU OF MINES Price One Dollar Free to Residents of Arizona Bulletin 181 1970 THE UNIVERSITY OF ARIZONA TUCSON TABLE OF CONT'ENTS EIements .___ 1 FOREWORD Sulfides ._______________________ 9 As a service about mineral matters in Arizona, the Arizona Bureau Sulfosalts ._. .___ __ 22 of Mines, University of Arizona, is pleased to reprint the long-standing booklet on MINERALS OF ARIZONA. This basic journal was issued originally in 1941, under the authorship of Dr. Frederic W. Galbraith, as Simple Oxides .. 26 a bulletin of the Arizona Bureau of Mines. It has moved through several editions and, in some later printings, it was authored jointly by Dr. Gal Oxides Containing Uranium, Thorium, Zirconium .. .... 34 braith and Dr. Daniel J. Brennan. It now is being released in its Fourth Edition as Bulletin 181, Arizona Bureau of Mines. Hydroxides .. .. 35 The comprehensive coverage of mineral information contained in the bulletin should serve to give notable and continuing benefits to laymen as well as to professional scientists of Arizona. Multiple Oxides 37 J. D. Forrester, Director Arizona Bureau of Mines Multiple Oxides Containing Columbium, February 2, 1970 Tantaum, Titanium .. .. .. 40 Halides .. .. __ ____ _________ __ __ 41 Carbonates, Nitrates, Borates .. .... .. 45 Sulfates, Chromates, Tellurites .. .. .. __ .._.. __ 57 Phosphates, Arsenates, Vanadates, Antimonates .._ 68 First Edition (Bulletin 149) July 1, 1941 Vanadium Oxysalts ...... .......... 76 Second Edition, Revised (Bulletin 153) April, 1947 Third Edition, Revised 1959; Second Printing 1966 Fourth Edition (Bulletin 181) February, 1970 Tungstates, Molybdates.. _. .. .. .. 79 Silicates ... -
801 38#4-Aožt00-2170-02
801 The Canadian Mineralogist Vol. 38, pp. 801-808 (2000) BOLEITE: RESOLUTION OF THE FORMULA, K Pb26 Ag9 Cu24 Cl62 (OH)48 MARK A. COOPER AND FRANK C. HAWTHORNE§ Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada ABSTRACT 3 The crystal structure of boleite, K Pb26 Ag9 Cu24 Cl62 (OH)48, a 15.288(2) Å, V 3574(1) Å , Pm 3¯ m, Z = 1, has been refined to an R-index of 2.2% based on 884 observed (5) reflections collected with MoK␣ X-radiation. A new site was resolved, and site-scattering refinement showed it to be occupied by a scattering species with 19 epfu (electrons per formula unit); this result is in accord with complete occupancy of this site by K. Potassium was detected by electron-microprobe analysis, but the amount determined is only ~50% of the amount indicated by site-scattering refinement. However, the refinement results show K to be disordered within a large cage in the structure, and the electron-beam bombardment probably induces rapid migration of K within the structure. Infrared spectroscopy shows that there is no H2O present in the structure. The H-sites were determined during refinement, and a sensible H-bonding scheme results. Keywords: boleite, crystal structure, new formula, hydrogen bonding. SOMMAIRE 3 Nous avons affiné la structure cristalline de la boléite, K Pb26 Ag9 Cu24 Cl62 (OH)48, a 15.288(2) Å, V 3574(1) Å , Pm¯3m, Z = 1, jusqu’à un résidu R de 2.2% en utilisant 884 réflexions observées (5) prélevées avec rayonnement MoK␣. -
The Relationship Between Mineral Composition
Mineralogical Magazine, April 2016, Vol. 80(2), pp. 291–310 The relationship between mineral composition, crystal structure and paragenetic sequence: the case of secondary Te mineralization at the Bird Nest drift, Otto Mountain, California, USA 1,* 2 3 4 5 ANDREW G. CHRISTY ,STUART J. MILLS ,ANTHONY R. KAMPF ,ROBERT M. HOUSLEY ,BRENT THORNE AND 6 JOE MARTY 1 Department of Applied Mathematics, Research School of Physics & Engineering, Mills Rd, Australian National University, Canberra, ACT 0200, Australia 2 Geosciences, Museum Victoria, GPO Box 666, Melbourne 3001, Victoria, Australia 3 Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, CA 90007, USA 4 Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA 91125, USA 5 53898 S. Newport Circle, Bountiful, UT 84010, USA 6 65199 E. Silver Oak Road, Salt Lake City, UT 84108, USA [Received 1 February 2015; Accepted 19 May 2015; Associate Editor: Ian Graham] ABSTRACT An unusually diverse array of 25 secondary Te oxysalt minerals has been documented from Otto Mountain, California, and 18 of these from the Bird Nest drift sublocality. A paragenetic sequence for these minerals is proposed, using observed overgrowth relationships plus spatial association data and data from other localities. Apart from Te and O, the components Pb, Cu and H are essential in the majority of the minerals. The atomic Cu/Te ratio decreases through the paragenetic sequence. This, and the occurrence of minerals − 2À 2À 3+ with additional components such as Cl ,CO3 ,SO4 and Fe at an intermediate stage, suggests non- monotonic evolution of the parent fluids, reflecting differing access to or spatial distribution of various components.