Commodities, Part 5 Strontium, Sodium Sulfate, Trona (Soda Ash), Talc, Lithium, Summary Comments Safety Reminders
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Fire Retardancy of Polypropylene/Kaolinite Composites Marcos Batistella, Belkacem Otazaghine, Rodolphe Sonnier, Carlos Petter, José-Marie Lopez-Cuesta
Fire retardancy of polypropylene/kaolinite composites Marcos Batistella, Belkacem Otazaghine, Rodolphe Sonnier, Carlos Petter, José-Marie Lopez-Cuesta To cite this version: Marcos Batistella, Belkacem Otazaghine, Rodolphe Sonnier, Carlos Petter, José-Marie Lopez-Cuesta. Fire retardancy of polypropylene/kaolinite composites. Polymer Degradation and Stability, Elsevier, 2016, 129, pp.260-267. 10.1016/j.polymdegradstab.2016.05.003. hal-02906432 HAL Id: hal-02906432 https://hal.archives-ouvertes.fr/hal-02906432 Submitted on 26 May 2021 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. Fire retardancy of polypropylene/kaolinite composites * Marcos Batistella a, c, , Belkacem Otazaghine b, Rodolphe Sonnier b, Carlos Petter c, Jose-Marie Lopez-Cuesta b a Federal University of Santa Catarina, R. Eng. Agronomico^ Andrei Cristian Ferreira, s/n e Trindade, Florianopolis, SC, CEP 88040-900, Brazil b Ecole des Mines d’Ales, Centre des Materiaux (C2MA) e Pole^ Materiaux Polymeres Avances, 6 Avenue de Clavieres, 30319, Ales Cedex, France c Federal University of Rio Grande do Sul, Av. Bento Gonçalves, 9500, Porto Alegre, CEP 91501-970, Brazil abstract In this study the influence of surface modification of kaolinite with trisilanolisooctyl Polyhedral Oligo- SilSesquioxane (POSS) in polypropylene composites was evaluated in terms of thermal stability and fire retardancy and compared with talc. -
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 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. -
Gaylussite Na2ca(CO3)2 • 5H2O C 2001-2005 Mineral Data Publishing, Version 1
Gaylussite Na2Ca(CO3)2 • 5H2O c 2001-2005 Mineral Data Publishing, version 1 Crystal Data: Monoclinic. Point Group: 2/m. As flattened wedge-shaped crystals with dominant {110}, {011}, {001}, smaller {010}, {100}, {101}, {112}; also as prismatic to dipyramidal crystals elongated along [100], to 6 cm. Physical Properties: Cleavage: On {110}, perfect; on {001}, imperfect. Fracture: Conchoidal. Tenacity: Very brittle. Hardness = 2.5–3 D(meas.) = 1.991 D(calc.) = 1.991 Dehydrates with efflorescence in dry air; slowly decomposes in H2O leaving CaCO3 as calcite or aragonite. Optical Properties: Transparent to translucent. Color: Colorless to pale yellow or pale gray, white; colorless in transmitted light. Streak: White to pale gray. Luster: Vitreous. Optical Class: Biaxial (–). Orientation: X = b; Z ∧ c = –15◦. Dispersion: r< v,strong, crossed. α = 1.444 β = 1.516 γ = 1.523 2V(meas.) = 34◦ Cell Data: Space Group: C2/c. a = 11.589 b = 7.780 c = 11.207 β = 102.5◦ Z=4 X-ray Powder Pattern: John Hay, Jr. Well No. 1, Wyoming, USA. 6.403 (100), 3.18 (80), 2.70 (80), 2.61 (80), 1.91 (80), 2.49 (70), 1.98 (70) Chemistry: (1) (2) CO2 30.02 29.72 SiO2 0.08 Fe2O3 0.03 MnO 0.01 MgO 0.01 CaO 19.02 18.94 Na2O 20.40 20.93 H2O 30.47 30.41 insol. 0.16 Total 100.20 100.00 • (1) Taboos-nor salt lake, Mongolia. (2) Na2Ca(CO3)2 5H2O. Occurrence: Typically in evaporites or shales from alkali lakes; rarely in veinlets cutting alkalic igneous rocks. -
Talc and Pyrophyllite
TALC AND PYROPHYLLITE By Robert L. Virta Domestic survey data and tables were prepared by Raymond I. Eldridge III, statistical assistant, and the world production table was prepared by Glenn J. Wallace, international data coordinator. The mineral talc is a hydrous magnesium silicate. A massive recommended against listing asbestiform talc and talcose rock is called steatite, and an impure massive variety is nonasbestiform talc in its 10th report on carcinogens (U.S. known as soapstone. Talc is used commercially because of its Department of Health and Human Services, Public Health fragrance retention, luster, purity, softness, and whiteness. Service, 2001; National Paint and Coatings Association, Other commercially important properties of talc are its chemical January 2001, NTP skips over talc, accessed January 8, 2001, at inertness, high dielectric strength, high thermal conductivity, URL http://www.paint.org/ind_issue/current/jan/issue05.htm). low electrical conductivity, and oil and grease adsorption. In 2000, the U.S. Department of Defense authorized the Major markets for talc are ceramics, paint, paper, and plastics. disposal of 907 metric tons (t) of block and lump talc, which is Pyrophyllite is a hydrous aluminum silicate with a structure the entire uncommitted inventory in that category, from the similar to talc. Such properties as chemical inertness, high National Defense Stockpile. dielectric strength, high melting point, and low electrical conductivity make it useful for ceramic and refractory Production applications. Talc.—In 2000, seven companies operating nine mines in five Legislation and Government Programs States produced soapstone, steatite, and talc. All were open pit mines. The producers were, in decreasing order of production, The National Toxicology Program (NTP) of the U.S. -
New Mineral Names*
American Mineralogist, Volume 75, pages 240-246, 1990 NEW MINERAL NAMES* JOHN L. JAMBOR CANMET, 555 Booth Street, Ottawa, Ontario KIA OGI, Canada EDWARD S. GREW Department of Geological Sciences, University of Maine, Orono, Maine 04469, U.S.A. Baiyuneboite-(Ce) the formula for cordylite-(Ce) requires revision such that Pigqiu Fu, Xlanze Su (1987) Baiyuneboite-A new min- cordylite-(Ce) and baiyuneboite-(Ce) may be identical. The eral. Acta Mineralogica Sinica, 7, 289-297 (in Chinese, Chairman therefore withdrew the approval and asked that English abstract). the authors withhold publication of their description of Pingqiu Fu, Youhua Kong, Guohong Gong, Meicheng baiyuneboite-(Ce) until the matter could be resolved. The Shao, Jinzi Qian (1987) The crystal structure of bai- request, unfortunately, was ignored. J.L.J. yuneboite-(Ce). Acta Mineralogica Sinica, 7, 298-304 (in Chinese, English abstract). Diaoyudaoite* Electron-microprobe analyses of ten grains, whose va- lidity was checked by single-crystal X-ray methods prior Shunxi Shen, Lirong Chen, Anchun Li, Tailu Dong, Qiu- to analysis, gave an average ofNa20 4.73, CaO 1.04, BaO huo Huang, Wenqiang Xu (1986) Diaoyudaoite-A new 20.38, Ce20, 24.21, La20, 10.92, Pr20, 0.62, Nd20, 10.04, mineral. Acta Mineralogica Sinica, 6, 224-227 (in Gd20, 0.13, F 2.50, C02 (by gas chromatography) 24.64, Chinese, English abstract). o == F 1.05, sum 98.16 wt%, corresponding to Nal.OS- The average of 13 electron-microprobe analyses gave (BaO.94CaO.I,)n07( Ce I.OSLao.4sN do.42Pr 0.0'Gdo.OI)"1.99F 0.9'C,.97- Na20 4.54, AI20, 93.00, Cr20, 1.95, MgO 0.10, CaO 0.10, 012.07'ideally NaBaCe2F(CO')4' The mineral occurs as yel- SiOz 0.23, K20 0.12, sum 100.04 wt%, corresponding to low, irregular grains 0.3 to 3 mm in size, frequently as (N ao.87Ko.ozMgo.02CaO.01)ro.92(AllO.84CrO.lsSio.02)"'1.01 0,7, ide- thin hexagonal tablets. -
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. -
Swelling Capacity of Mixed Talc-Like/Stevensite Layers in White/Green Clay
This is a preprint, the final version is subject to change, of the American Mineralogist (MSA) Cite as Authors (Year) Title. American Mineralogist, in press. DOI: https://doi.org/10.2138/am-2020-6984 1 1 Plagcheck: no concerns 2 Tables?: 3 small 3 Word Count: ~9,100 4 Prod notes: make sure tables in file before RE 5 6 7 8 Swelling capacity of mixed talc-like/stevensite layers in white/green clay 9 infillings (‘deweylite’/‘garnierite’) from serpentine veins of faulted 10 peridotites, New Caledonia 11 REVISION 2 12 Lionel FONTENEAU 1, Laurent CANER 2*, Sabine PETIT 2, Farid JUILLOT 3, Florian 13 PLOQUIN 3, Emmanuel FRITSCH 3 14 15 1Corescan Pty Ltd, 1/127 Grandstand Road, 6104 Ascot, WA, Australia 16 2 Université de Poitiers, Institut de Chimie des Milieux et Matériaux de Poitiers, IC2MP UMR 17 7285 CNRS, 5 rue Albert Turpain, TSA51106, 86073 Poitiers cedex 9, France 18 * Corresponding author, e-mail: [email protected] 19 3 Institut de Minéralogie, de Physique des Matériaux et de Cosmochimie (IMPMC), Sorbonne 20 Universités – Université Pierre et Marie Curie UPMC, UMR CNRS 7590, Museum National 21 d’Histoire Naturelle, UMR IRD 206, 101 Promenade Roger Laroque, Anse Vata, 98848, 22 Nouméa, New Caledonia 23 24 25 Abstract: White (Mg-rich) and green (Ni-rich) clay infillings (‘deweylite’/‘garnierite’) found 26 in serpentine veins of faulted peridotite formations from New Caledonia consist of an intimate 27 mixture of fine-grained and poorly ordered 1:1 and 2:1 layer silicates, commonly referred to 28 as non-expandable serpentine-like (SL) and talc-like (TL) minerals. -
Carbon Mineral Ecology: Predicting the Undiscovered Minerals of Carbon
American Mineralogist, Volume 101, pages 889–906, 2016 Carbon mineral ecology: Predicting the undiscovered minerals of carbon ROBERT M. HAZEN1,*, DANIEL R. HUMMER1, GRETHE HYSTAD2, ROBERT T. DOWNS3, AND JOSHUA J. GOLDEN3 1Geophysical Laboratory, Carnegie Institution, 5251 Broad Branch Road NW, Washington, D.C. 20015, U.S.A. 2Department of Mathematics, Computer Science, and Statistics, Purdue University Calumet, Hammond, Indiana 46323, U.S.A. 3Department of Geosciences, University of Arizona, 1040 East 4th Street, Tucson, Arizona 85721-0077, U.S.A. ABSTRACT Studies in mineral ecology exploit mineralogical databases to document diversity-distribution rela- tionships of minerals—relationships that are integral to characterizing “Earth-like” planets. As carbon is the most crucial element to life on Earth, as well as one of the defining constituents of a planet’s near-surface mineralogy, we focus here on the diversity and distribution of carbon-bearing minerals. We applied a Large Number of Rare Events (LNRE) model to the 403 known minerals of carbon, using 82 922 mineral species/locality data tabulated in http://mindat.org (as of 1 January 2015). We find that all carbon-bearing minerals, as well as subsets containing C with O, H, Ca, or Na, conform to LNRE distributions. Our model predicts that at least 548 C minerals exist on Earth today, indicating that at least 145 carbon-bearing mineral species have yet to be discovered. Furthermore, by analyzing subsets of the most common additional elements in carbon-bearing minerals (i.e., 378 C + O species; 282 C + H species; 133 C + Ca species; and 100 C + Na species), we predict that approximately 129 of these missing carbon minerals contain oxygen, 118 contain hydrogen, 52 contain calcium, and more than 60 contain sodium. -
The Cordierite Formation in Mechanically Activated Talc-Kaoline-Alumina-Basalt-Quartz Ceramic System D
Vol. 127 (2015) ACTA PHYSICA POLONICA A No. 4 Proceedings of the 4th International Congress APMAS2014, April 24-27, 2014, Fethiye, Turkey The Cordierite Formation in Mechanically Activated Talc-Kaoline-Alumina-Basalt-Quartz Ceramic System D. Kirsever*, N. Karakus, N. Toplan, H.O. Toplan Sakarya University, Metalurgy and Materials Engineering, 54187 Sakarya, Turkey The powder mixtures of Talc-Kaolinite-Alumina-Basalt-Quartz were mechanically activated in a planetary ball mill for 1 hour. The structural alterations and thermal behaviour of the powder mixture were examined by X-ray diraction (XRD), scanning electron microscopy (SEM) and thermal analysis (TG-DTA). The results showed that the mechanical activation led to amorphisation and decreased the temperature of cordierite formation. DOI: 10.12693/APhysPolA.127.1042 PACS: 81.05.Je 1. Introduction a high-energy ball mill. In this process, a small quantity of the blended elemental powder mixture is loaded into a Cordierite, which chemical composition is container, along with the grinding media, and the whole 2MgO 2Al O 5SiO , is one of the phases of the · 2 3· 2 mass is agitated at a high speed for a predetermined ternary MgOSiO Al O system, along with mullite, 2 2 3 length of time [5]. The mechano-activation treatment cristobalite, tridymite, enstatite, forsterite, sapphirine, might promote: the amorphization of treated material, etc. Cordierite-based materials have a great importance noticeable change of the microstructure, size and shape in modern technology due to their excellent properties, of particles, etc. Furthermore, ultra-ne grinding kinetic such as low thermal expansion coecient, high refrac- investigation indicates the mechano-chemical reduction toriness, low dielectric constant, high thermal shock of the original particles of talc/mica, which appears to resistance and good mechanical properties [1]. -
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.