What Are Refractory Metals?
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A Contribution to the Chemistry of Rhenium
U. S. DEPARTMENT OF COMMERCE NATIONAL BUREAU OF STANDARDS RESEARCH PAPER RP999 Part of Journal of Research of the J'Xational Bureau of Standards, Volume 18, May 1937 A CONTRIBUTION TO THE CHEMISTRY OF RHENIUM . By C. E. F. Lundell and H. B. Knowles ABSTRACT A study of the behavior of rhenium when dilute solutions of potassium per rhenate are acidified with sulphuric acid, cooled, and passed through the Jones reductor, indicates that rhenium forms a compound in which it has a valency of minus one, and that the rhenium in this compound is oxidized to a valency of plus one if the diluted sulphuric acid solution is protected from oxygen and warmed to approximately 50° C. In the course of the investigation, it was also found (1) that rhenium can be electrodeposited from diluted (5+95) sulphuric acid solution; (2) that deposits are slightly contaminated; and (3) that the deposited metal can be oxidized directly to perrhenic acid by exposure to moist air, oxygen, or by making the deposit the anode in a water solution. CONTENTS Page 1. Introduction ___ _____________________ ____ __ __ _____ ___ ___ _____ _____ 629 II. ExperimentaL _ ___ _ _ _ _ _ _ _ _ _ _ _ _ __ _ _ __ ___ _ _ _ _ _ __ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ _ 630 1. Reagents, reductor, and reductor technique ___________________ 630 2. Oxidation of the reduced compound _______________ ___________ 631 3. Potentiometric titrations _______________ ___ ___ ______ ___ _____ 634 4. -
Evolution and Understanding of the D-Block Elements in the Periodic Table Cite This: Dalton Trans., 2019, 48, 9408 Edwin C
Dalton Transactions View Article Online PERSPECTIVE View Journal | View Issue Evolution and understanding of the d-block elements in the periodic table Cite this: Dalton Trans., 2019, 48, 9408 Edwin C. Constable Received 20th February 2019, The d-block elements have played an essential role in the development of our present understanding of Accepted 6th March 2019 chemistry and in the evolution of the periodic table. On the occasion of the sesquicentenniel of the dis- DOI: 10.1039/c9dt00765b covery of the periodic table by Mendeleev, it is appropriate to look at how these metals have influenced rsc.li/dalton our understanding of periodicity and the relationships between elements. Introduction and periodic tables concerning objects as diverse as fruit, veg- etables, beer, cartoon characters, and superheroes abound in In the year 2019 we celebrate the sesquicentennial of the publi- our connected world.7 Creative Commons Attribution-NonCommercial 3.0 Unported Licence. cation of the first modern form of the periodic table by In the commonly encountered medium or long forms of Mendeleev (alternatively transliterated as Mendelejew, the periodic table, the central portion is occupied by the Mendelejeff, Mendeléeff, and Mendeléyev from the Cyrillic d-block elements, commonly known as the transition elements ).1 The periodic table lies at the core of our under- or transition metals. These elements have played a critical rôle standing of the properties of, and the relationships between, in our understanding of modern chemistry and have proved to the 118 elements currently known (Fig. 1).2 A chemist can look be the touchstones for many theories of valence and bonding. -
Corrosion of Refractories by Denis A
A Chapter in the Refractories Handbook, edited by Charles A. Schacht, and to be published by Marcel Dekker, Inc., New York, NY 10016 Corrosion of Refractories by Denis A. Brosnan, PhD, PE Clemson University Clemson, SC 29634-0971 Introduction Refractories are used at elevated temperatures for structural purposes and they are used in many cases to contain a high temperature corrosive environment. This corrosive environment usually contains liquid (melted) phases that participate in chemical reactions with the refractory at the elevated temperatures resulting in refractory consumption or wear. It is usually not immediately obvious, but the oxidation and reduction state of the environment (as “redox” conditions or oxygen “activity”) can participate in and influence the chemical reactions that take place. Along with chemical reactions during corrosion, physical changes occur that may be accelerated by the corrosion process. Corrosion of refractories can be defined for the purposes of this discussion as follows: Corrosion of Refractories – refractory wear by loss of thickness and mass from the exposed face of the refractory as a consequence of chemical attack by a corroding fluid in a process in which the refractory and the corroding fluid react approaching chemical equilibrium in the zone of contact between the refractory and the fluid. It is an essential point that corrosion reactions proceed in a direction toward localized chemical equilibrium. This means that phase equilibrium diagrams can be used to analyze corrosion situations and to predict chemical strategies to minimize corrosion and wear rates. This gives persons interested in refractory corrosion two options. The first is to view corrosion as a chemical and physical process without a detailed application of phase equilibrium diagrams – called the “phenomenological approach”. -
Untraditional Synthesis of Boron-Containing Superhard and Refractory Materials - a Review B
G.J. E.D.T., Vol. 2(1) 2013:21-26 ISSN 2319 – 7293 UNTRADITIONAL SYNTHESIS OF BORON-CONTAINING SUPERHARD AND REFRACTORY MATERIALS - A REVIEW B. Agyei-Tuffour1,2, E. Annan1,2, E. R. Rwenyagila1, E. Ampaw1, E. Arthur1, K. Mustapha1, S. Kolawole1, W. O. Soboyejo1,3, & D. D. Radev1,4 1Department of Materials Science and Engineering, African University of Science and Technology, Abuja-Nigeria 2Department of Materials Science and Engineering, Private Mail Bag, University of Ghana, Legon-Accra. 3Department of Mechanical and Aerospace Engineering, Princeton University, USA. 4Institute of General and Inorganic Chemistry, Bulgaria Academy of Sciences, Sofia-Bulgaria Abstract Boron-containing ceramics find large application in production of superhard and high-temperature materials with application in nuclear and aerospace techniques, military industry etc. The synthesis methods are decisive for the complexity of chemical, morphological and technological properties of these materials. The traditional high-temperature synthesis methods have some disadvantages leading to inconstancy of the product composition due to the boron evaporation, degradation of the furnace materials and contamination of the products, high energy losses etc. Here we show the advantages of some untraditional synthesis methods like direct mechanical synthesis and self propagating high-temperature synthesis (SHS) in the production of titanium diboride (TiB2), zirconium diboride (ZrB2) and production of dense boron carbide (B4C) based materials. Using SEM, TEM, XRD and analytical chemical methods, it was shown that diborides of titanium and zirconium have appropriate properties for production of dense ceramic materials. Using the method of mechanically-assisted sintering high-dense B4C-based ceramic materials was obtained. It was shown that the mechanical properties of materials obtained by pressureless sintering are close or overcome the corresponding properties of boron carbide densified by the method of hot pressing. -
The Periodic Table of Elements
The Periodic Table of Elements 1 2 6 Atomic Number = Number of Protons = Number of Electrons HYDROGENH HELIUMHe 1 Chemical Symbol NON-METALS 4 3 4 C 5 6 7 8 9 10 Li Be CARBON Chemical Name B C N O F Ne LITHIUM BERYLLIUM = Number of Protons + Number of Neutrons* BORON CARBON NITROGEN OXYGEN FLUORINE NEON 7 9 12 Atomic Weight 11 12 14 16 19 20 11 12 13 14 15 16 17 18 SODIUMNa MAGNESIUMMg ALUMINUMAl SILICONSi PHOSPHORUSP SULFURS CHLORINECl ARGONAr 23 24 METALS 27 28 31 32 35 40 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 POTASSIUMK CALCIUMCa SCANDIUMSc TITANIUMTi VANADIUMV CHROMIUMCr MANGANESEMn FeIRON COBALTCo NICKELNi CuCOPPER ZnZINC GALLIUMGa GERMANIUMGe ARSENICAs SELENIUMSe BROMINEBr KRYPTONKr 39 40 45 48 51 52 55 56 59 59 64 65 70 73 75 79 80 84 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 RUBIDIUMRb STRONTIUMSr YTTRIUMY ZIRCONIUMZr NIOBIUMNb MOLYBDENUMMo TECHNETIUMTc RUTHENIUMRu RHODIUMRh PALLADIUMPd AgSILVER CADMIUMCd INDIUMIn SnTIN ANTIMONYSb TELLURIUMTe IODINEI XeXENON 85 88 89 91 93 96 98 101 103 106 108 112 115 119 122 128 127 131 55 56 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 CESIUMCs BARIUMBa HAFNIUMHf TANTALUMTa TUNGSTENW RHENIUMRe OSMIUMOs IRIDIUMIr PLATINUMPt AuGOLD MERCURYHg THALLIUMTl PbLEAD BISMUTHBi POLONIUMPo ASTATINEAt RnRADON 133 137 178 181 184 186 190 192 195 197 201 204 207 209 209 210 222 87 88 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 FRANCIUMFr RADIUMRa RUTHERFORDIUMRf DUBNIUMDb SEABORGIUMSg BOHRIUMBh HASSIUMHs MEITNERIUMMt DARMSTADTIUMDs ROENTGENIUMRg COPERNICIUMCn NIHONIUMNh -
Research Memorandum
RM ESOG21 NACA RESEARCH MEMORANDUM SO:ME PROPER TIES OF BER YLLIUM OXIDE AND BERYLLIUM OXIDE - COLUMBIUM CERAMALS By C. F. Robards and J. J. Gangler " Lewis Flight Propulsion Laboratory Cleveland, Ohio NATIONAL ADVISORY COMMITTEE FOR AERONAUTICS WASHINGTON March 2 , 1951 NACA RM E5OG21 NATIONAL ADVISORY COMMITTEE FOR AERONAUTICS RESEARCH MEMORANDUM SOME PROPERTIES OF BERYLLIUM OXIDE AND BERYLLIUM OXIDE - COLUMBIUM CERAMALS By C. F. Robards and J. J . Gangler SUMMARY Because of the potentially excellent refractory properties of beryllium oxide, a brief investigation was made of its short time tensile strength at a temperature of 18000 F and relative thermal-shock resistance from temperatures of 18000 and 2000° F to room temperature. The effect of additions of 2, 5, 8, 10, 12, and 15 percent by weight of columbium metal on the thermal-shock resistance of beryllium oxide was studied. Metallographic examination indicated that the metallic phase coalesced into pockets. Beryllium oxide had a tensile strength as high as 6160 :9ounds per square inch at 18000 F. The original columbium underwent a phase change, as indicated by X-ray analysis of the ceramals. The addition of columbium up to 15 percent by weight failed to improve the resistance to thermal shock. The phase change and the failure of the columbium to 'vet the beryllium oxide may explain the poor thermal-shock resistance of these ceramals. INTRODUCTION Beryllium oxide BeO has the highest thermal-shock resistance of the better-known oxide bodies. In an effort to extend the life of this material in thermal shock, an attempt was made at the NACA Lewis laboratory to use a metallic binder in the manner that has been successful in the carbide-tool industry. -
Aluminum Electrolytic Vs. Polymer – Two Technologies – Various Opportunities
Aluminum Electrolytic vs. Polymer – Two Technologies – Various Opportunities By Pierre Lohrber BU Manager Capacitors Wurth Electronics @APEC 2017 2017 WE eiCap @ APEC PSMA 1 Agenda Electrical Parameter Technology Comparison Application 2017 WE eiCap @ APEC PSMA 2 ESR – How to Calculate? ESR – Equivalent Series Resistance ESR causes heat generation within the capacitor when AC ripple is applied to the capacitor Maximum ESR is normally specified @ 120Hz or 100kHz, @20°C ESR can be calculated like below: ͕ͨ͢ 1 1 ͍̿͌ Ɣ Ɣ ͕ͨ͢ ∗ ͒ ͒ Ɣ Ɣ 2 ∗ ∗ ͚ ∗ ̽ 2 ∗ ∗ ͚ ∗ ̽ ! ∗ ̽ 2017 WE eiCap @ APEC PSMA 3 ESR – Temperature Characteristics Electrolytic Polymer Ta Polymer Al Ceramics 2017 WE eiCap @ APEC PSMA 4 Electrolytic Conductivity Aluminum Electrolytic – Caused by the liquid electrolyte the conductance response is deeply affected – Rated up to 0.04 S/cm Aluminum Polymer – Solid Polymer pushes the conductance response to much higher limits – Rated up to 4 S/cm 2017 WE eiCap @ APEC PSMA 5 Electrical Values – Who’s Best in Class? Aluminum Electrolytic ESR approx. 85m Ω Tantalum Polymer Ripple Current rating approx. ESR approx. 200m Ω 630mA Ripple Current rating approx. 1,900mA Aluminum Polymer ESR approx. 11m Ω Ripple Current rating approx. 5,500mA 2017 WE eiCap @ APEC PSMA 6 Ripple Current >> Temperature Rise Ripple current is the AC component of an applied source (SMPS) Ripple current causes heat inside the capacitor due to the dielectric losses Caused by the changing field strength and the current flow through the capacitor 2017 WE eiCap @ APEC PSMA 7 Impedance Z ͦ 1 ͔ Ɣ ͍̿͌ ͦ + (͒ −͒ )ͦ Ɣ ͍̿͌ ͦ + 2 ∗ ∗ ͚ ∗ ͍̿͆ − 2 ∗ ∗ ͚ ∗ ̽ 2017 WE eiCap @ APEC PSMA 8 Impedance Z Impedance over frequency added with ESR ratio 2017 WE eiCap @ APEC PSMA 9 Impedance @ High Frequencies Aluminum Polymer Capacitors have excellent high frequency characteristics ESR value is ultra low compared to Electrolytic’s and Tantalum’s within 100KHz~1MHz E.g. -
High-Temperature Properties of Magnesia-Refractory Brick Treated with Oxide and Salt Solutions
Q [R I 1898o I PLEASEDO NOT REMOVEFROM LIBRARY ()' ~ Bureau of Mines Report of Investigations/1985 ~ ~ High-Temperature Properties of Magnesia-Refractory Brick Treated With Oxide and Salt Solutions By James P. Bennett UNITED STATES DEPARTMENT OF THE INTERIOR Report of Investigations 8980 High-Temperature Properties of Magnesia-Refractory Brick Treated With Oxide and Salt Solutions By James P. Bennett UNITED STATES DEPARTMENT OF THE INTERIOR Donald Paul Hodel, Secretary BUREAU OF MINES Robert C. Horton, Director Research at the Tusca loo sa Research Center is carried out under a memorandum of agreement be tween . the Bureau of Mines, U.S. Department of the Interior, and the University of Alaba ma. Library of Congress Cataloging in Publication Data: Bennett, James P. (James Philip), 1951- High-temperature properties of magnesia-refractory brick treated with oxide and salt solutions. (Report of investigations 8980) Bi bl iography: p. 11. Supt. of Docs. no.: I 28.23: 8980. 1. Magnesia brick-Thermal properties. 2. Oxides. 3. Salt. 1. Title. II. Series: Report of investigations (United States. Bureau of Mines) ; 8980. TN23.C43 (TA418.26] 622s l669',821 85-600138 CONTENTS AbsIntroduction................................................................... tract ••••••••••••••••••••••••••••••••••••••••••••••••••••••••••••••••••••••• 2 Refractory brick and sample preparation........................................ 2 Treatment procedure--solutions and techniques.................................. 4 Results and discussion........................................................ -
Electric Arc Furnace (EAF) Refractory Concept Solutions
STEEL INDUSTRY ELECTRIC ARC FURNACES STEEL INDUSTRY CALDERYS PERFORMANCE YOU CAN TRUST For all industries with extreme temperatures and working conditions, Calderys is there for you. Combining a global network with local expertise, we offer customised solutions wherever you are: from monolithic refractory to bricks and precast shapes to a full range of engineering and installation services. KEY POINTS Over 100 years of refractory experience Over 2 300 employees across 33 countries 19 plants in 16 countries totaling 600 000 tons capacity Annual revenue of over € 500 million 1 Global Technology Centre and 15 Customisation Labs 150 major projects implemented every year Wholly-owned subsidiary of Imerys Group 2 STEEL INDUSTRY OUR VALUE TO THE STEELMAKING INDUSTRY The world leader in monolithic refractory solutions, Calderys has a full product and service portfolio to adapt to the refractory needs of steelmakers. We ensure that we propose products most suitable for your process requirements and deliver to you superior refractory performance and reliable services. We are able to do so by combining our innovative product range and modern installation techniques with end-to-end project management. Value Optimisation Offering tailor-made solutions that meet the commercial and technical requirements for optimal performance. Complete Refractory Solutions We offer a full range of refractory products to meet the process needs of modern Steelmaking. Technology Expertise Ensuring the best possible equipment availability and productivity at the lowest total refractory cost per ton of steel produced, whilst adhering to strict environmental and safety regulations in operations. 3 STEEL INDUSTRY CALDERYS A TRUSTED SUPPLIER IN THE STEEL INDUSTRY A world leader in Refractory Solutions, Calderys has the complete product and service portfolio for all applications. -
Electrodeposition of Alloys Or Compounds in Molten Salts and Applications
Journal of Mining and Metallurgy, 39 (1‡2) B (2003) 177 - 200. ELECTRODEPOSITION OF ALLOYS OR COMPOUNDS IN MOLTEN SALTS AND APPLICATIONS P. Taxil, P. Chamelot, L. Massot and C. Hamel Laboratoire de Génie Chimique, Département Procédés Electrochimiques et Matériaux, CNRS UMR 5503, Université Paul-Sabatier, 118 route de Narbonne, 31062 Toulouse Cedex 04, France (Received 12 February 2003; accepted 18 April 2003) Abstract This article deals with the different modes of preparation of alloys or intermetallic compounds using the electrodeposition in molten salts, more particularly molten alkali fluorides. The interest in this process is to obtain new materials for high technology, particularly the compounds of reactive components such as actinides, rare earth and refractory metals. Two ways of preparation are considered: (i) electrocoating of the more reactive metal on a cathode made of the noble one and reaction between the two metals in contact, and (ii) electrocoating on an inert cathode of the intermetallic compound by coreduction of the ions of each elements. The kinetic is controlled by the reaction at the electrolyte interface. A wide bibliographic survey on the preparation of various compounds (intermetallic compounds, borides, carbides…) is given and a special attention is paid to the own experience of the authors in the preparation of these compounds and interpreta- tion of their results. Keywords: Electrosynthesis, alloys, intermetallic, compounds, molten salts, alkali fluorides, co-reduction, reactive electrodeposition 1. Introduction Laboratories of chemical engineering are often interested in high technology processes to prepare coatings of new materials or compounds; most of these compounds J. Min. Met. 39 (1 ‡ 2) B (2003) 177 taxil.indd 1 6/26/03, 12:06 PM P. -
Metallurgy Materials Programs
WASH-1181-73 METALLURGY AND MATERIALS PROGRAMS 0 FY 1973 UNITED STATES ATOMIC ENERGY COMMISSION DIVISION of PHYSICAL RESEARCH LEGAL NOTICE This report was prepared as an account of work sponsored by the United States Government. Neither the United States nor the United States Atomic Energy Commission. nor any of their employees, nor any of their contractors, subcontractors, or their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness or usefulness of any information, apparatus, product or process disclosed, or represents that its use would not infringe privately owned rights. WASH-1181-73 METALLURGY AND MATERIALS PROGRAMS Fiscal Year 1973 July 1973 U. S. Atomic Energy Commission Division of Physical Research FORWORD The Metallurgy and Materials Program constitutes one portion of a wide range of research supported by the AEC Division of Physical Research. Other programs are administered by the Division's Chemistry, High Energy Physics, and Physics and Mathematics Offices. Metallurgy and Materials research is supported primarily at AEC National Laboratories and Univer- sities. The research covers a wide spectrum of scientific and engineering areas of interest to the Atomic Energy Commission and is conducted generally by personnel trained in the disciplines of Solid State Physics, Metallurgy, Ceramics, and Physical Chemistry. This report contains a listing of all research underway in FY 1973 together with a convenient index to the program. Donald K. Stevens Assistant Director (for Metallurgy and Materials Programs) Division of Physical Research i INTRODUCTION The purpose of this report is to provide a convenient compilation and index of the AEC's Metallurgy and Materials Programs. -
Interactions of Lanthanides and Liquid Alkali Metals for “Liquid-Like” Lanthanide Transport in U-Zr Fuel
Interactions of Lanthanides and Liquid Alkali Metals for “Liquid-Like” Lanthanide Transport in U-Zr Fuel THESIS Presented in Partial Fulfillment of the Requirements for the Degree Master of Science in the Graduate School of The Ohio State University By Jeremy Payton Isler Graduate Program in Nuclear Engineering The Ohio State University 2017 Master's Examination Committee: Dr. Jinsuo Zhang, Advisor Dr. Marat Khafizov, Co-Advisor Copyrighted by Jeremy Payton Isler 2017 Abstract One of the major limitations in achieving increased burnup in metallic U-Zr nuclear fuel is Fuel-Cladding Chemical Interaction (FCCI). The migration of the fission product lanthanides from within the fuel to the peripheral is one of the major contributors to FCCI. A “liquid-like” transport mechanism proposes the lanthanide transport is aided by liquid cesium and liquid sodium in the pores of the fuel and at the fuel peripheral. The purpose of this thesis was to provide additional experimental evidence towards this proposed mechanism. This thesis investigated the interaction between the lanthanides and cesium and sodium, with a focus on the solubility of the lanthanides in these liquid alkali metals. First, a prediction of the solubility was calculated using the Miedema model. This prediction was then compared to the inversion crucible solubility experiment performed in this thesis. The solubility experiment studied the temperature and liquid-composition dependence of the lanthanides in liquid sodium, cesium and sodium-cesium mixtures. In addition, the solubility in mixtures shows the various alkali metals concentration effect on the solubility. With the results of differential scanning calorimetry (DSC) experiments, updated phase diagrams for sodium-neodymium and cesium-neodymium were obtained from the experimental data in this thesis.