Aluminum Discovered: H.C. Oersted in 1825 Name: from Alum, Used By
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Recycling of Hazardous Waste from Tertiary Aluminium Industry in A
CORE Metadata, citation and similar papers at core.ac.uk Provided by Digital.CSIC 1 Recycling of hazardous waste from tertiary aluminium 2 industry in a value-added material 3 4 Laura Gonzalo-Delgado1, Aurora López-Delgado1*, Félix Antonio López1, Francisco 5 José Alguacil1 and Sol López-Andrés2 6 7 1Nacional Centre for Metallurgical Research, CSIC. Avda. Gregorio del Amo, 8. 28040. 8 Madrid. Spain. 9 2Dpt. Crystallography and Mineralogy. Fac. of Geology. University Complutense of 10 Madrid. Spain. 11 *Corresponding author e-mail: [email protected] 12 13 Abstract 14 15 The recent European Directive on waste, 2008/98/EC seeks to reduce the 16 exploitation of natural resources through the use of secondary resource management. 17 Thus the main objective of this paper is to explore how a waste could cease to be 18 considered as waste and could be utilized for a specific purpose. In this way, a 19 hazardous waste from the tertiary aluminium industry was studied for its use as a raw 20 material in the synthesis of an added value product, boehmite. This waste is classified as 21 a hazardous residue, principally because in the presence of water or humidity, it releases 22 toxic gases such as hydrogen, ammonia, methane and hydrogen sulphide. The low 23 temperature hydrothermal method developed permits the recovery of 90% of the 24 aluminium content in the residue in the form of a high purity (96%) AlOOH (boehmite). 25 The method of synthesis consists of an initial HCl digestion followed by a gel 26 precipitation. In the first stage a 10% HCl solution is used to yield a 12.63 g.l-1 Al3+ 27 solution. -
The Solubility of Aluminium in Melts Containing Aluminium Halides
THE SOLUBILITY OF ALUMINIUM IN MELTS CONTAINING ALUMINIUM HALIDES A Thesis presented for the degree of Doctor of Philosophy in the University of London by John Dyson Usher London, May 1965 ABSTRACT A technique for measuring the solubility of aluminium in NaF-A1F3 and Nall-A1F3+5%A1203 melts has been developed using a refractory titanium boride- carbide crucible and a gas volumetric method of analysis. Experiments were conducted at 10209 1100 and 1180°C; in both systems no change in solubility limit was detected over the experimental composition range of 25.6 - 36.6 and 25.8 - 31.9 mol % AlF3 respectively. The figures in the pure fluoride are 0.022 0.041 and 0.072 wt %; in the alumina melts 0.073, 0.121 and 0.169 wt %. Solution mechanisms have been suggested which account for the observed behaviour, and an attempt has been made to interpret the current inefficiency process in the reduction cell in terms of the results. CONTENTS 1. INTRODUCTION Page 1.1 Aluminium Reduction Cell - Brief Description 1 1.2 Current Efficiency 3 1.2.1 Measurement 3 1.2.2 Cell Variables and Current Efficiency 5 1.2.2 Postulated Mechanisms of Metal Lose 6 1.3 Origins of Present Work 7 1.3.1 Information Required 7 1.3.A Preliminary Theoretical Approach 9 1.4 Metal-Molten Salt Solutions 11 1.4.1 General 11 1.4.2 Nature of Metal-Molten Salt Solutions 16 1.4.3 Extent of Solubility 19 1.4.4 Effect of Foreign Ions on Metal Solubility 23 1.5 Structure of Cryolite and Cryolite-Alumina Melts 25 1.5.1 Pure Molten Cryolite 25 1.5.2 Cryolite-Alumina Melts 33 1.6 Thermodynamics of Aluminium+Cryolite 40 1.6.1 Equilibrium 1.6(i): Experimental 40 1.6.2 Equilibrium 1.6(i): Calculations 42 1.6.3 Equilibrium 1.6(ii) 45 1.7 Previous Experimental Work 46 1.7.1 Analysis by Metal Weight Loss 48 1.7.2 Gas Volumetric Method 52 2. -
Recovery of Carbon and Cryolite from Spent Pot Lining of Aluminium Reduction Cells by Chemical Leaching
Trans. Nonferrous Met. Soc. China 22(2012) 222−227 Recovery of carbon and cryolite from spent pot lining of aluminium reduction cells by chemical leaching SHI Zhongning, LI Wei, HU Xianwei, REN Bijun, GAO Bingliang, WANG Zhaowen School of Materials and Metallurgy, Northeastern University, Shenyang 110004, China Received 29 November 2010; accepted 8 October 2011 Abstract: A twostep alkalineacidic leaching process was conducted to separate the cryolite from spent pot lining and to purify the carbon. The influencing factors of temperature, time, and the ratio of liquid to solid in alkaline and acidic leaching were investigated. The results show that the recovery of soluble compounds of Na3AlF6 and Al2O3 dissolving into the solution during the NaOH leaching is 65.0%,and the purity of carbon reaches 72.7%. During the next step of HCl leaching, the recovery of soluble compounds of CaF2 and NaAl11O17 dissolving into the HCl solution is 96.2%, and the carbon purity increases to 96.4%. By mixing the acidic leaching solution and the alkaline leaching solution, the cryolite precipitates under a suitable conditions of pH value 9 at 70 °C for 2 h. The cryolite precipitating rate is 95.6%, and the purity of Na3AlF6 obtained is 96.4%. Key words: spent pot lining; recovery; chemical leaching; aluminium electrolysis method separates the carbon and fluoride according to 1 Introduction the difference in solubility, density and surface properties between carbon and fluorides. For example, the froth With a rapid development of the primary aluminium flotation technology is a typically physical separation industry, more and more spent pot lining (SPL) is process for SPL treatment [3]. -
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 Structure and Vibrational Spectroscopy of Cryolite, Na3alf6 Cite This: RSC Adv., 2020, 10, 25856 Stewart F
RSC Advances PAPER View Article Online View Journal | View Issue The structure and vibrational spectroscopy of cryolite, Na3AlF6 Cite this: RSC Adv., 2020, 10, 25856 Stewart F. Parker, *a Anibal J. Ramirez-Cuesta b and Luke L. Daemenb Cryolite, Na3[AlF6], is essential to commercial aluminium production because alumina is readily soluble in molten cryolite. While the liquid state has been extensively investigated, the spectroscopy of the solid state has been largely ignored. In this paper, we show that the structure at 5 K is the same as that at Received 31st May 2020 room temperature. We use a combination of infrared and Raman spectroscopies together with inelastic Accepted 1st July 2020 neutron scattering (INS) spectroscopy. The use of INS enables access to all of the modes of Na3[AlF6], DOI: 10.1039/d0ra04804f including those that are forbidden to the optical spectroscopies. Our spectral assignments are supported rsc.li/rsc-advances by density functional theory calculations of the complete unit cell. Introduction In view of the technological importance of cryolite, we have Creative Commons Attribution 3.0 Unported Licence. carried out a comprehensive spectroscopic investigation and 1 Cryolite, Na3[AlF6], occurs naturally as a rare mineral. Histori- report new infrared and Raman spectra over extended temper- cally, it was used as a source of aluminium but this has been ature and spectral ranges and the inelastic neutron scattering superseded by bauxite (a mixture of the Al2O3 containing (INS) spectrum. The last of these is observed for the rst time minerals boehmite, diaspore and gibbsite), largely because of and enables access to all of the modes of Na3[AlF6]. -
Synthesis of Alum from Aluminum
Synthesis of Alum from Aluminum Taken from Central Oregon College Chemistry Manual OBJECTIVES: To carry out a series of reactions to transform a piece of aluminum foil into crystals of alum and to gain familiarity with using stoichiometry to determine the yield for the reaction. SAFETY AND DISPOSAL: Strong acids and bases are corrosive and should be handled with care. Immediately wipe up any spills and wash hands with plenty of soap and water. Work in the mini-hoods whenever possible to avoid breathing in fumes. All solutions can be disposed of down the sink with running water. The alum can be safely disposed of in the trash but has a number of uses and can be used for other laboratories, place alum crystals into the designated container. INTRODUCTION: Aluminum is a material that you may have had some experience with and paid little attention to, but has some very interesting characteristics. Here are some fun facts about aluminum metal: 1. Aluminum is the third most abundant element in the earth's crust. 2. The supply of aluminum ore is not inexhaustible. 3. The winning, or extraction of the metallic form an impure ionic source, of aluminum from aluminum ore is very costly from an energy point of view. 4. The above point explains why Napoleon III used aluminum dinnerware for his state dinners. Lesser guests were served on plates of gold or silver. 5. The process of obtaining pure metallic aluminum from aluminum oxide in a reasonably energy efficient manner, which made it possible for aluminum to be the inexpensive metal we know today, was developed in a home laboratory shortly after the chemist finished his undergraduate degree. -
Cryolithionite and Li in the Cryolite Deposit Ivigtut, South Greenland
Cryolithionite and Li in the Cryolite Deposit Ivigtut, South Greenlan d By HANS PAULY Matematisk-fysiske Meddelelser 42 : 1 Det Kongelige Danske Videnskabernes Selskab The Royal Danish Academy of Sciences and Letter s Commissioner : Munksgaard • Copenhagen 1986 Abstract Cryolithionite always occurred as single crystals in cryolite : idiomorphic, subidiomorphic and, rarely , anhedral . It was found in siderite- cryolite ; in a variety of this type : black cryolite with red-brown Th - containing fluorite, siderite etc . (BCrbF) ; in pure, white cryolite ; in cryolite veining the wall rocks . I t belongs to the period in which siderite- cryolite formed . Analyses of 268 cryolite samples gave 92 ppm Li (min. 19, rnax . 224 ppm) . Cryolite from samples with cryolithionite : 81 ppm, cryolite from BCrbF with no cryolithionite : 185 ppm . Cryolithionite seems to have formed by exsolution from cryolite with 155 ppm Li or more . The high con- traction of cryolite on cooling (1 vol% pr. 100°C) may have given rise to low-pressure regions within the cryolite where cryolithionite (d= 2 .77) replaced cryolite (d- 2 .97) after formation of the complicated twin structures in the cryolite - at or below 450°C . The compound Na 2LiAIF 6 (d=3 .02) is not present in th e deposit. HANS PAULY Technical University of Denmark bg .204, DK-2800 Lyngb y Denmark Keywords: Cryolithionite, Li in cryolite, siderite- cryolite, Th-containing fluorite, black cryolite, Ivigtut , South-Greenland . List of Content s Introduction 3 Cryolithionite in the deposit 3 In situ observations of cryolithionite 6 The cryolite deposit at Ivigtut 7 Appearance of cryolithionite, its outer shape, mineral and fluid inclusions 1 1 Formation of cryolithionite 1 7 Li in cryolite and other minerals of the Ivigtut deposit 1 8 Cryolithionite formed by exsolution from cryolite 1 9 Acknowledgments 2 3 Literature 23 © Det kongelige Danske Videnskabernes Selskab 1986 Printed in Denmark by Bianco Lunos Bogtrykkeri A/S . -
Bauxite and Aluminum Handbook Commodities and Export Projections Division Economic Analysis and Projectuonsdepartment
I Bauxite and Aluminum Handbook Commodities and Export Projections Division Economic Analysis and ProjectUonsDepartment 3 . February 1981 TABLE OF CONTENTS Page No. I. CHARACTERISTICSOF BAUXITE/ALUMINA/ALUIMINUM.............. 1 A. Introduction .......... 1 B. Definition of Products .......t ........ ......... * 1 C. Uses ....... ..... 2 D. Technology . ... ... 5 II. THE LOCATION OF THE INDUSTRY....................... #...... I A. Production...... ... .. ......................... .. 1 B. Consumption....... ... .. to. 6 C. Trade.................................. 8 III. THE STRUCTURE OF THE INDUSTRY........................ 1 A. Organization ................... .- .. ....... ... 1 B. Marketing .............# ............................ 4 O ZIV.ECONOMIC PARAMETERS FOR MARKET ANALYSIS OF THE BAUXITE-ALUMINUMINDUSTRY ......................................... 1 A. Demand and Supply Elasticities........ ........... 1 B. Price DeterminationMechanisms ....................... 2 V. MARKET PRICES FOR BAUXITE, ALUMINA AND ALUMINUM.......... 1 A. Bauxite................................ .... .*............... 1 B. Alumina .............................................. 7 C. Aluminum,, ........**.............. #.... **.*..................... 7 VI. SPECIAL ISSUES........................................... 1 A. Shipping................... .... .0.0.......................1 B. The InternationalBauxite Association (IBA) .......... 3 C. The Integrated Program for Commodities............... 4 D. United States Government Stockpile................... 5 February1981 -
Leaching Behavior of Lithium-Bearing Bauxite with High-Temperature Bayer Digestion Process in K2O-Al2o3-H2O System
metals Article Leaching Behavior of Lithium-Bearing Bauxite with High-Temperature Bayer Digestion Process in K2O-Al2O3-H2O System Dongzhan Han 1,2 , Zhihong Peng 1,*, Erwei Song 2 and Leiting Shen 1 1 School of Metallurgy and Environment, Central South University, Changsha 410083, China; [email protected] (D.H.); [email protected] (L.S.) 2 Zhengzhou Non-Ferrous Metals Research Institute Co. Ltd. of CHALCO, Zhengzhou 450041, China; [email protected] * Correspondence: [email protected] Abstract: Lithium is one of the secondary mineral elements occurring in bauxite. The behavior of lithium-bearing bauxite in the digestion process was investigated, and the effect of digestion conditions on the extraction rates of lithium was studied. The results demonstrate that the mass ratio of the added CaO to bauxite, the KOH concentration, and the digestion temperature had a significant effect on the lithium extraction efficiency. An L9(34) orthogonal experiment demonstrated that the order of each factor for lithium extraction from primary to secondary is lime dosage, caustic concentration, and reaction temperature. Under the optimal conditions (t = 60 min, T = 260 ◦C, r(K2O) = 280 g/L, and 16% lime dosage), the leaching efficiencies of lithium and alumina are 85.6% and 80.09%, respectively, with about 15% of lithium entering into red mud. The findings of this study maybe useful for controlling lithium content in alumina products and lithium recovery from the Citation: Han, D.; Peng, Z.; Song, E.; Bayer process. Shen, L. Leaching Behavior of Lithium-Bearing Bauxite Keywords: lithium-bearing bauxite; digestion; K2O-Al2O3-H2O system withHigh-Temperature Bayer Digestion Process in K2O-Al2O3-H2O System. -
New Mineral Names*
American Mineralogist, Volume 73, pages 1492-1499. 1988 NEW MINERAL NAMES* JOHN L. JAMBOR CANMET, 555 Booth Street, Ottawa, Ontario KIA OGI, Canada ERNST A. J. BURKE lnstituut voor Aardwetenschappen, Vrije Universitiete, De Boelelaan 1085, 1081 HV, Amsterdam, Netherlands T. SCOTT ERCIT, JOEL D. GRICE National Museum of Natural Sciences, Ottawa, Ontario KIA OM8, Canada Acuminite* prismatic to acicular crystals that are up to 10 mm long and 0.5 H. Pauly, O.Y. Petersen (1987) Acuminite, a new Sr-fluoride mm in diameter, elongate and striated [001], rhombic to hex- from Ivigtut, South Greenland. Neues Jahrb. Mineral. Mon., agonal in cross section, showing {l00} and {l10}. Perfect {100} 502-514. cleavage, conchoidal fracture, vitreous luster, H = 4, Dm'.. = 2.40(5) glcm3 (pycnometer), Dcale= 2.380 glcm3 for the ideal Wet-chemical analysis gave Li 0.0026, Ca 0.0185, Sr 37.04, formula, and Z = 4. Optically biaxial positive, a = 1.5328(4), (3 Al 11.86, F 33.52, OH (calc. from anion deficit) 6.82, H20 (calc. = 1.5340(4), 1.5378(4), 2 Vmoa,= 57(2)°, 2 Vcale= 59°; weak assuming 1 H20 in the formula) 7.80, sum 97.06 wt%, corre- 'Y = dispersion, r < v; Z = b, Y A c = -10°. X-ray structural study sponding to Sro98AIl.o2F.o7(OH)o.93H20. The mineral occurs as indicated monoclinic symmetry, space group C21c, a = 18.830(2), aggregates of crystals shaped like spear points and about I mm b= I 1.517(2), c= 5.190(I)A,{3 = 100.86(1)°. A Guinierpowder long. -
Uilitgd States Patent [19] [11] Patent Number: 4,647,386 Jamison [45] Date of Patent: Mar
UIlItGd States Patent [19] [11] Patent Number: 4,647,386 Jamison [45] Date of Patent: Mar. 3, 1987 [54] INTERCALATED TRANSITION METAL Attorney, Agent, or Firm-—Robert E. Harris BASED SOLID LUBRICATING COMPOSITION AND METHOD OF SO [57] ABSTRACT , FORMING A solid lubricating composition and method for form ing such a composition are disclosed. The composition [76] Inventor: Warren E. Jamison, 528 Parkview Ave., Golden, Colo. 80401 is formed by intercalating a transition metal that has been chemically reacted with chalcogen to form a lay [21] App]. No.: 538,137 ered structure. The transition metal is selected from [22] Filed: Oct. 3, 1983 niobium, tantalum, tungsten and/or an alloy including one or more, and the transition metal is chemically [51] Int. Cl.4 ......................................... .. C10M 125/22 combined with chalcogen selected from sulfur, sele [52] US. Cl. ...................... .. 252/25; 423/561 R nium and/or a combination which can also include [5 8] Field of Search ..................... .. 252/25; 423/561 R tellurium to form a layered transition metal dischal [56] References Cited cogenide prior to intercalation with a metal, preferably U.S. PATENT DOCUMENTS a coinage metal. The effect of intercalation is to expand the crystal lattice to create a composition having excel 3,573,204 3/1971 Van Wyk ............................ .. 252/12 Thompson 252/12 lent lubricating characteristics the performance of 3,763,043 10/1973 which is not adversely effected by operation in a high 3,769,210 10/1973 Cais et a1. ........ .. 252/25 4,040,917 8/1977 Whittingham . .. 204/36 temperature environment. 4,094,893 6/ 1978 Dines ................................. -
Synergy of Alum and Chlorine Dioxide for Curbing Disinfection Byproduct Formation Potential at Central Arkansas Water Corey W
University of Arkansas, Fayetteville ScholarWorks@UARK Theses and Dissertations 5-2012 Synergy of Alum and Chlorine Dioxide for Curbing Disinfection Byproduct Formation Potential at Central Arkansas Water Corey W. Granderson University of Arkansas, Fayetteville Follow this and additional works at: http://scholarworks.uark.edu/etd Part of the Environmental Engineering Commons, and the Water Resource Management Commons Recommended Citation Granderson, Corey W., "Synergy of Alum and Chlorine Dioxide for Curbing Disinfection Byproduct Formation Potential at Central Arkansas Water" (2012). Theses and Dissertations. 310. http://scholarworks.uark.edu/etd/310 This Thesis is brought to you for free and open access by ScholarWorks@UARK. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of ScholarWorks@UARK. For more information, please contact [email protected], [email protected]. SYNERGY OF ALUM AND CHLORINE DIOXIDE FOR CURBING DISINFECTION BYPRODUCT FORMATION POTENTIAL AT CENTRAL ARKANSAS WATER SYNERGY OF ALUM AND CHLORINE DIOXIDE FOR CURBING DISINFECTION BYPRODUCT FORMATION POTENTIAL AT CENTRAL ARKANSAS WATER A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Civil Engineering By Corey W. Granderson University of Arkansas Bachelor of Science in Civil Engineering, 2008 May 2012 University of Arkansas Abstract Central Arkansas Water (CAW), the water utility for Little Rock, AR, draws their source water from Lake Maumelle and Lake Winona. To curb disinfection byproduct (DBP) formation, CAW has begun retrofitting their two plants to use chlorine dioxide as an alternative primary disinfectant followed by free chlorine secondary disinfection in the distribution system. In this study, fluorescence parallel factor (PARAFAC) analysis was combined with free chlorine simulated distribution system (SDS) tests and DBP formation potential (DBPFP) tests to study the benefit of chlorine dioxide primary disinfection (CDPD) with alum coagulation.