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Standard X-Ray Diffraction Powder Patterns
NBS MONOGRAPH 25 — SECTION 1 Standard X-ray Diffraction U.S. DEPARTMENT OF COMMERCE NATIONAL BUREAU OF STANDARDS THE NATIONAL BUREAU OF STANDARDS Functions and Activities The functions of the National Bureau of Standards are set forth in the Act of Congress, March 3, 1901, as amended by Congress in Public Law 619, 1950. These include the development and maintenance of the national standards of measurement and the provision of means and methods for making measurements consistent with these standards; the determination of physical constants and properties of materials; the development of methods and instruments for testing materials, devices, and structures; advisory services to government agencies on scien- tific and technical problems; invention and development of devices to serve special needs of the Government; and the development of standard practices, codes, and specifications. The work includes basic and applied research, development, engineering, instrumentation, testing, evaluation, calibration services, and various consultation and information services. Research projects are also performed for other government agencies when the work relates to and supplements the basic program of the Bureau or when the Bureau's unique competence is required. The scope of activities is suggested by the listing of divisions and sections on the inside of the back cover. Publications The results of the Bureau's research are published either in the Bureau's own series of publications or in the journals of professional and scientific societies. The Bureau itself publishes three periodicals available from the Government Printing Office: The Journal of Research, published in four separate sections, presents complete scientific and technical papers; the Technical News Bulletin presents summary and preliminary reports on work in progress; and Basic Radio Propagation Predictions provides data for determining the best frequencies to use for radio communications throughout the world. -
Tundrite-(Ce) Na3(Ce; La)4(Ti; Nb)2(Sio4)2(CO3)3O4(OH) ² 2H2O C 2001 Mineral Data Publishing, Version 1.2 ° Crystal Data: Triclinic
Tundrite-(Ce) Na3(Ce; La)4(Ti; Nb)2(SiO4)2(CO3)3O4(OH) ² 2H2O c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Triclinic. Point Group: 1: Crystals acicular along [001] and °attened on 010 , to 3 cm; as stellate groups and spherulitic masses. Twinning: On 010 , producing f g f g pseudorhombohedra. Physical Properties: Cleavage: Pronounced on 010 . Fracture: Splintery. f g Tenacity: Brittle. Hardness = 3 D(meas.) = 3.70{4.12 D(calc.) = 4.06 » Optical Properties: Transparent. Color: Brownish yellow, greenish yellow to bright light green. Streak: Yellowish gray. Luster: Vitreous to adamantine. Optical Class: Biaxial (+). Pleochroism: Weak; X = pale yellow; Z = greenish yellow. Orientation: Z c = 4 {14 . ® = 1.743 ¯ = 1.80 ° = 1.88 2V(meas.) = 76 ^ ± ± ± Cell Data: Space Group: P 1: a = 7.533(4) b = 13.924(6) c = 5.010(2) ® = 99±52(2)0 ¯ = 70±50(3)0 ° = 100± 59(2)0 Z = 1 X-ray Powder Pattern: Il¶³maussaq intrusion, Greenland. 13.49 (100), 2.505 (100), 3.448 (90), 2.766 (90), 3.535 (80), 6.784 (70), 1.914 (70) Chemistry: (1) SiO2 10.03 TiO2 12.20 La2O3 8.57 Ce2O3 24.38 Nd2O3 10.25 RE2O3 5.80 Nb2O5 3.44 CaO 0.75 Na2O 8.20 CO3 16.38 Total [100.00] (1) Il¶³maussaq intrusion, Greenland; by electron microprobe, C con¯rmed by loss on ignition; original analysis given as elements, here recalculated to oxides, corresponding to Na3:17(Ce1:78Nd0:73La0:63RE0:41Ca0:16)§=3:71(Ti1:83Nb0:31)§=2:14(SiO4)2:00(CO3)3:27O4:25: Occurrence: In pegmatite veins associated with nepheline syenites. -
Electromigration in Thin Films of Aluminium"
Co / Y A thesis entitled "ELECTROMIGRATION IN THIN FILMS OF ALUMINIUM" by Stephen Roberts B.Sc., A.R.C.S. Submitted for the Degree of Doctor of Philosophy of the University of London Imperial College of Science and Technology London 1982 2 ABSTRACT Electromigration is a common cause of failure of the aluminium thin film metallizations used in many microelectronic devices and circuits. The objective of the present work was to draw correlations between processing parameters, micro- structure and susceptibility to electromigration failure of vacuum-evaporated aluminium films on amorphous Si O^. The chemical composition of the Al - Si C>2 interface was examined using x-ray photoelectron spectroscopy, Auger electron spectroscopy and transmission electron microscopy and diffraction. The effects of substrate surface preparation and temperature on Al - Si O^ interfacial reaction were investigated. Reduction of the Si02 by the aluminium, resulting in the production of polycrystalline silicon and Tj - alumina, was found to occur under the conditions prevalent in many industrial metallization processes. The implications of Al-Si O2 reaction for device reliability are discussed. A range of techniques, including transmission and scanning electron microscopy and grazing incidence x-ray diffraction, were used to characterize the grain size, preferred orientation and surface topography of aluminium films deposited onto Si C>2 under various conditions. 1 yum thick aluminium films were found to have a ^111) fibre texture and the mean grain size ranged from less than 0.5yjm for deposition at 300 K, to ** 5 yum, for deposition at 675 K. Some thinner films were also examined, and trends in grain size and orientation with thickness were established. -
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 -
First Terrestrial Occurrence of Titanium
875 Thz Caradian M fuc ralo g is t Vol.35, pp. 875-885(1997) FIRSTTERRESTRIAL OCCURRENCE OF TITANIUM.RICH PYRRHOTITE, MARCASITEAND PVRITEIN A FENITIZEDXENOLITH FROMTHE KHIBINA ALKALINE COMPLEX. RUSSIA ANDREI Y. BARKOVT nxp KAUKO V.O. LAAJOKI Irxtiruteof Geosciencesand Astrorcmy, University of Oula FIN-90570OuIW FinLand YT]RIP.MEN'SHIKOV Geological Instirute, Kola Science Cente, Russian Acadenry of Scimces, 14 Fersman Street, Apatity 1M200 , Russia TUOMO T. AI.APIETI Instituteof Geoscierrcesand Astrotnnry, University of Ouh+FN-90570 OuIu Finlnnl SEPPOJ. SryONEN Instiarcof ElcctronOptics, University of OuhaFN-90570 Ouh+ Finlnnd ABSTRACT The first terrestrial titanium-rich sulfides, the fust natural niobium-rich sulfide FeMgSe, fluorine-rich (ca. 6 wt.Vo D end-memberphlogopite (S().04 wLTo FeO) and ferroan alabandite occurlocally in aheterogeneous xenolit\ enclosed within nepheline syenite in the l(hifiaa alkalins gs6plex, Kola Peninsul4 northwestem Russia- This assemblage is exclusively associated with an alkali-feldspar-rich rock, probably fenite. Associat€d ninerals include corundum, Nb-Zr-bearing rutile and monazite. The maximum Ti content reaches 3.9 w.7o in pynhotite and 2 wt.7o in marcasite and pyrite, which represent prducts of replacement of the pynhotite. Titanium is distributed rather homogeneously within single grains of the pyrrhotite; however, a strong grain-to-gain variation is observed. The Tl-rich sulfides invariably contrin an elevated level ofvanadium (0.2-0 .4 wr.Vo).T\e results indicate that both Ti and V enter into solid solution in the sulfides. Presumably, there is an environmental similarity between the occurrences ofTl-bearing sulfides in trftibina and in meteorites (enstatite chondrites), where Tl-bearing hoilite occurs. -
Cafetite, Ca[Ti2o5](H2O): Crystal Structure and Revision of Chemical Formula
American Mineralogist, Volume 88, pages 424–429, 2003 Cafetite, Ca[Ti2O5](H2O): Crystal structure and revision of chemical formula SERGEY V. K RIVOVICHEV,1,* VICTOR N. YAKOVENCHUK,2 PETER C. BURNS,3 YAKOV A. PAKHOMOVSKY,2 AND YURY P. MENSHIKOV2 1Department of Crystallography, St. Petersburg State University, University Embankment 7/9, St. Petersburg 199034, Russia 2Geological Institute, Kola Science Centre, Russian Academy of Sciences, Fersmana 14, 184200-RU Apatity, Russia 3Department of Civil Engineering and Geological Sciences, University of Notre Dame, Notre Dame, Indiana 46556-0767, U.S.A. ABSTRACT The crystal structure of cafetite, ideally Ca[Ti2O5](H2O), (monoclinic, P21/n, a = 4.9436(15), b = 12.109(4), c = 15.911(5) Å, b = 98.937(5)∞, V = 940.9(5) Å3, Z = 8) has been solved by direct methods and refined to R1 = 0.057 using X-ray diffraction data collected from a crystal pseudo-merohedrally twinned on (001). There are four symmetrically independent Ti cations; each is octahedrally coordi- nated by six O atoms. The coordination polyhedra around the Ti cations are strongly distorted with individual Ti-O bond lengths ranging from 1.743 to 2.223 Å (the average <Ti-O> bond length is 1.98 Å). Two symmetrically independent Ca cations are coordinated by six and eight anions for Ca1 and Ca2, respectively. The structure is based on [Ti2O5] sheets of TiO6 octahedra parallel to (001). The Ca atoms and H2O groups are located between the sheets and link them into a three-dimensional struc- ture. The structural formula of cafetite confirmed by electron microprobe analysis is Ca[Ti2O5](H2O), . -
Third-Generation Synchrotron X-Ray Diffraction of 6- M Crystal of Raite, Na
Proc. Natl. Acad. Sci. USA Vol. 94, pp. 12263–12267, November 1997 Geology Third-generation synchrotron x-ray diffraction of 6-mm crystal of raite, 'Na3Mn3Ti0.25Si8O20(OH)2z10H2O, opens up new chemistry and physics of low-temperature minerals (crystal structureymicrocrystalyphyllosilicate) JOSEPH J. PLUTH*, JOSEPH V. SMITH*†,DMITRY Y. PUSHCHAROVSKY‡,EUGENII I. SEMENOV§,ANDREAS BRAM¶, CHRISTIAN RIEKEL¶,HANS-PETER WEBER¶, AND ROBERT W. BROACHi *Department of Geophysical Sciences, Center for Advanced Radiation Sources, GeologicalySoilyEnvironmental, and Materials Research Science and Engineering Center, 5734 South Ellis Avenue, University of Chicago, Chicago, IL 60637; ‡Department of Geology, Moscow State University, Moscow, 119899, Russia; §Fersman Mineralogical Museum, Russian Academy of Sciences, Moscow, 117071, Russia; ¶European Synchrotron Radiation Facility, BP 220, 38043, Grenoble, France; and UOP Research Center, Des Plaines, IL 60017 Contributed by Joseph V. Smith, September 3, 1997 ABSTRACT The crystal structure of raite was solved and the energy and metal industries, hydrology, and geobiology. refined from data collected at Beamline Insertion Device 13 at Raite lies in the chemical cooling sequence of exotic hyperal- the European Synchrotron Radiation Facility, using a 3 3 3 3 kaline rocks of the Kola Peninsula, Russia, and the 65 mm single crystal. The refined lattice constants of the Monteregian Hills, Canada (2). This hydrated sodium- monoclinic unit cell are a 5 15.1(1) Å; b 5 17.6(1) Å; c 5 manganese silicate extends the already wide range of manga- 5.290(4) Å; b 5 100.5(2)°; space group C2ym. The structure, nese crystal chemistry (3), which includes various complex including all reflections, refined to a final R 5 0.07. -
New Mineral Names*,†
American Mineralogist, Volume 100, pages 1649–1654, 2015 New Mineral Names*,† DMITRIY I. BELAKOVSKIY1 AND OLIVIER C. GAGNE2 1Fersman Mineralogical Museum, Russian Academy of Sciences, Leninskiy Prospekt 18 korp. 2, Moscow 119071, Russia 2Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada IN THIS ISSUE This New Mineral Names has entries for 10 new minerals, including debattistiite, evdokimovite, ferdowsiite, karpovite, kolskyite, markhininite, protochabournéite, raberite, shulamitite, and vendidaite. DEBATTISTIITE* for 795 unique I > 2σ(I) reflections] corner-sharing As(S,Te)3 A. Guastoni, L. Bindi, and F. Nestola (2012) Debattistiite, pyramids form three-membered distorted rings linked by Ag atoms in triangular or distorted tetrahedral coordination. Certain Ag9Hg0.5As6S12Te2, a new Te-bearing sulfosalt from Len- genbach quarry, Binn valley, Switzerland: description and features of that linkage are similar to those in the structures of crystal structure. Mineralogical Magazine, 76(3), 743–750. trechmannite and minerals of pearceite–polybasite group. Of the seven anion positions, one is almost fully occupied by Te (Te0.93S0.07). The Hg atom is in a nearly perfect linear coordination Debattistiite (IMA 2011-098), ideally Ag9Hg0.5As6S12Te2, is a new mineral discovered in the famous for Pb-Cu-Ag-As-Tl with two Te/S atoms. One of five Ag sites and Hg site, which are bearing sulfosalts Lengenbach quarry in the Binn Valley, Valais, very close (separation 1.137 Å), are partially occupied (50%). Switzerland. Debattistiite has been identified in two specimens Thus there is a statistical distribution (50:50) between Hg(Te,S)2 from zone 1 of the quarry in cavities in dolomitic marble with and AgS2(Te,S)2 polyhedra in the structure. -
Geology and Age of the Lac a La Perdrix Fenite, Southern Gatineau District, Quebec
CA9700383 -4- Geology and age of the Lac a la Perdrix fenite, southern Gatineau district, Quebec D.D. Hogarth1 and Otto van Breemen2 Hogarth, D.D. and van Breemen, 0., 1996: Geology and age of the Lac a la Perdrix fenite, southern Gatineau district, Quebec; inRadiogenic Age and Isotopic Studies: Report 9; Geological Survey of Canada, Current Research 1995-F, p. 33-41. Abstract: The Lac a la Perdrix fenite lies in the Central Metasedimentary Belt of the Grenville Province. This 30 m wide fenite, adjacent to a narrow calciocarbonatite sill, replaces diopside-oligoclase gneiss and is composed of magnesio-arfvedsonite, aegirine, microcline, albite, and fluorapatite. Near the contact with carbonatite, it contains appreciable monazite and barite whereas aegirine virtually disappears. Fenitization probably took place early in the igneous stage of carbonatite development. A Pb/U monazite age of 1026 ± 2 Ma is thought to date fenite formation. Together with published data, this age shows that carbonatite intruded metamorphic rocks near the close of the Grenville Orogeny. Resume : La fenite de Lac a la Perdrix s'observe dans la ceinture metasedimentaire de la Province de Grenville. Cette fenite, mesurant 30 m de largeur et en position adjacente par rapport a un etroit filon-couche de calciocarbonatite, remplace un gneiss a diopside-oligoclase et se compose de magnesio-arfvedsonite, d'aegirine, de microcline, d'albite et de fluorapatite. Pres du contact avec la carbonatite, la fenite contient de la monazite et de la barytine en quantite appreciable, tandis que l'aegirine disparait pratiquement. La fenitisation a probablement eu lieu au debut de l'episode igne durant lequel s'est form6 la carbonatite. -
Oxygenic Bismuth Minerals in the NE Part of the Karkonosze Pluton (West Sudetes, SW Poland)
Acta Geologica Polonica, Vol. 68 (2018), No. 4, pp. 537–554 DOI: 10.1515/agp-2018-0016 Oxygenic bismuth minerals in the NE part of the Karkonosze pluton (West Sudetes, SW Poland) ANDRZEJ KOZŁOWSKI and WITOLD MATYSZCZAK* Faculty of Geology, University of Warsaw, Żwirki i Wigury 93, PL-02-089 Warszawa, Poland. *E-mail: [email protected] ABSTRACT: Kozłowski, A. and Matyszczak, W. 2018. Oxygenic bismuth minerals in the NE part of the Karkonosze pluton (West Sudetes, SW Poland). Acta Geologica Polonica, 68 (4), 537–554. Warszawa. The study presents fifteen oxygen-bearing secondary minerals of bismuth from the north-eastern part of the Variscan Karkonosze granitoid pluton in the northern zone of the Bohemian massif. The minerals were inves- tigated by optical, electron microprobe, classic chemical, XRD, IR absorption and fluid inclusion methods. The late, very low temperature epithermal solutions most probably caused formation of sillénite, kusachiite, bismoclite, bismutite, beyerite, kettnerite, pucherite, schumacherite, namibite and eulytite. Solutions dominated by supergene (meteoric) waters were the parents for bismite, russellite, koechlinite, ximengite and walpurgite. The paper also contains information on early research on the investigated minerals. Key words: Karkonosze granitoid pluton; Bismuth minerals; Secondary minerals; Oxidation; Vein; Pegmatite. FOREWORD joined by WM as the co-author, interested like him in further investigations of the Karkonosze pluton (see The paper presents an investigation of several ox- e.g., Matyszczak 2018). ygen-bearing minerals of bismuth, which were found in the Karkonosze granitoid, collected during field work by AK in 1976–1990. Most of the minerals were INTRODUCTION not known until the present either from the Polish part of the Karkonosze pluton, or from the area of The systematic scientific investigation of the Poland. -
Hectorite: Synthesis, Modification, Assembly and Applications Jing Zhang, Chun Hui Zhou, Sabine Petit, Hao Zhang
Hectorite: Synthesis, modification, assembly and applications Jing Zhang, Chun Hui Zhou, Sabine Petit, Hao Zhang To cite this version: Jing Zhang, Chun Hui Zhou, Sabine Petit, Hao Zhang. Hectorite: Synthesis, modification, assembly and applications. Applied Clay Science, Elsevier, 2019, 177, pp.114-138. 10.1016/j.clay.2019.05.001. hal-02363196 HAL Id: hal-02363196 https://hal-cnrs.archives-ouvertes.fr/hal-02363196 Submitted on 2 Dec 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. 1 Hectorite:Synthesis, Modification, Assembly and Applications 2 3 Jing Zhanga, Chun Hui Zhoua,b,c*, Sabine Petitd, Hao Zhanga 4 5 a Research Group for Advanced Materials & Sustainable Catalysis (AMSC), State Key Laboratory 6 Breeding Base of Green Chemistry-Synthesis Technology, College of Chemical Engineering, Zhejiang 7 University of Technology, Hangzhou 310032, China 8 b Key Laboratory of Clay Minerals of Ministry of Land and Resources of the People's Republic of 9 China, Engineering Research Center of Non-metallic Minerals of Zhejiang Province, Zhejiang Institute 10 of Geology and Mineral Resource, Hangzhou 310007, China 11 c Qing Yang Institute for Industrial Minerals, You Hua, Qing Yang, Chi Zhou 242804, China 12 d Institut de Chimie des Milieux et Matériaux de Poitiers (IC2MP), UMR 7285 CNRS, Université de 13 Poitiers, Poitiers Cedex 9, France 14 15 Correspondence to: Prof. -
Subject Index, Volume 81, 1996
American Mineralogist, Volume 81, pages 1543-1551, 1996 SUBJECT INDEX, VOLUME 81, 1996 Ag3TeS 1013 geikielite 485 florencite-(La) 1263 4°Ar 940 hornblende 928 glass 229 AuO(OH) 1282 hyttsj6ite 743 granitic melt 202 AuO(OH,Cl)onH20 766 kalsilite 561, 1360 kaolin 26 Achtarandite 516 kaolinite 26 migmatite 141 Afghanite 1003 kinoshitalite 485 orendite 229 Albite 92, 452, 789, 1133, 1344, laumontite 658 peridotite 79 1413 leonhardite 658, 668 rhyolite 158 Alkali feldspar 92, 719, 800, 1425 liandratite 1237 rhyolitic glass 158, 1249 Almandine 418 magnesiochromite 1186 sandstone 213 Altisite 516 magnesite 181 serpentinite 79 Aluminate sodalite 1375 medenbachite 505 volcanic glass 1176 Aluminosilicate glasses 265 muscovite 141, 1460 volcanic rocks 982 Alumoklyuchevskite 249 namuwite 238 Analysis, surface (mineral) Amphibole 135, 495, 1126 nanpingite 105 calcite 1 Analcime 39 nepheline 561, 1360 pyrite 261 Analysis, chemical (mineral) olivine 194, 1519 Anatexis 141 albite 92 omphacite 181 Androsite-(La) 735 alkali feldspar 719 orthopyroxene 676, 842 Ankerite 1141 almandine 418 pentlandite 187 Annite 475 amphibole 135, 495 phlogopite 202, 485,913 Annite-sanidine-magnetite 415 androsite-(La) 735 pigeonite 1166 Anorthoclase 1332 apatite 515 plagioclase 141, 913, 982, 1460 Antimonselite 1013 augite 1166 potassium feldspar 141 Antitaenite 766 bechererite 244 pumpellyite 603 Apatite 864, 1476 betafite 1237 pyralspitic garnet 418 Aragonite 181, 611 biopyribole 404 pyrite 119, 187 Arsenogorceixite 249 biotite 135, 141, 495, 1396, pyrope 418, 706 Asteroid