The Alkali Metals
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Low-Temperature Specific Heat in Caesium Borate Glasses Cristina Crupi, Giovanna D’Angelo, Gaspare Tripodo, Giuseppe Carini, A
Low-temperature specific heat in caesium borate glasses Cristina Crupi, Giovanna d’Angelo, Gaspare Tripodo, Giuseppe Carini, A. Bartolotta To cite this version: Cristina Crupi, Giovanna d’Angelo, Gaspare Tripodo, Giuseppe Carini, A. Bartolotta. Low- temperature specific heat in caesium borate glasses. Philosophical Magazine, Taylor & Francis, 2007, 87 (3-5), pp.741-747. 10.1080/14786430600910764. hal-00513746 HAL Id: hal-00513746 https://hal.archives-ouvertes.fr/hal-00513746 Submitted on 1 Sep 2010 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. Philosophical Magazine & Philosophical Magazine Letters For Peer Review Only Low-temperature specific heat in caesium borate glasses Journal: Philosophical Magazine & Philosophical Magazine Letters Manuscript ID: TPHM-06-May-0176.R1 Journal Selection: Philosophical Magazine Date Submitted by the 27-Jun-2006 Author: Complete List of Authors: Crupi, Cristina; Messina University, Physics D'Angelo, Giovanna; university of messina, physics Tripodo, Gaspare; Messina University, Physics carini, giuseppe; University of Messina, Dept of Physics Bartolotta, A.; Istituto per i Processi Chimico-Fisici, CNR amorphous solids, boson peak, calorimetry, disordered systems, Keywords: glass, specific heat, thermal properties Keywords (user supplied): http://mc.manuscriptcentral.com/pm-pml Page 1 of 13 Philosophical Magazine & Philosophical Magazine Letters 1 2 3 LOW TEMPERATURE SPECIFIC HEAT IN CAESIUM BORATE GLASSES 4 5 6 7 8 + 9 Cristina Crupi, Giovanna D’Angelo, Gaspare Tripodo, Giuseppe Carini and Antonio Bartolotta . -
Influence of Composition on Structure and Caesium Volatilisation from Glasses for HLW Confinement
Influence of Composition on Structure and Caesium Volatilisation from Glasses for HLW Confinement Benjamin Graves Parkinson B.Sc. (Hons.), M.Sc. A thesis submitted to the University of Warwick in partial fulfilment of the requirement for the degree of Doctor of philosophy Department of Physics November 2007 Contents Contents (i) List of Figures (vi) List of Tables (xv) List of Abbreviations (xvii) Acknowledgements (xviii) Declaration (xix) Abstract (xx) Chapter 1...................................................................................................................1 1 Introduction....................................................................................................1 1.1 Overview................................................................................................1 1.2 Aim of the work .....................................................................................1 1.3 References..............................................................................................5 Chapter 2...................................................................................................................7 2 Immobilisation of High Level Nuclear Waste.................................................7 2.1 Introduction............................................................................................7 2.2 High-Level Nuclear Waste......................................................................7 2.3 HLW Immobilisation..............................................................................8 2.3.1 -
United States Patent (19) 11 Patent Number: 4,640,713 Harris 45 Date of Patent: Feb
United States Patent (19) 11 Patent Number: 4,640,713 Harris 45 Date of Patent: Feb. 3, 1987 (54) TARNESHREMOVER/METAL POLISH 3,458,300 7/1969 Duvall et al. ........................... 106/3 FORMULATION COMPRISING A METAL 3,502,503 3/1970 Bartlo et al. ............................ 134/2 IODIDE, ANACID, AND WATER 3,518,098 6/1970 Ford et al. .............................. O6/3 3,582,366 6/1971 Brieger et al. 75 Inventor: Robert B. Harris, Racine County, 3,687,855 8/1972 Halpern..... Wis. 3,879,216 4/1975 Austin ..................................... 134/4 3,914, 161 10/1975 Yonezawa et al. a 73 Assignee: S. C. Johnson & Son, Inc., Racine, 3,997,460 12A1976 Sirine ............. Wis. 4,097,590 6/1978 Weisz ..... 4,116,699 9/1978 Rooney...... ...10673 21 Appl. No.: 672,966 4,207,310 6/1980 Langford ... ... 252A106 22) Filed: Nov. 19, 1984 4,444,756 4/984 Schlissier ........................... 252/106 51 Int. Cl. .......................... C09G 1/04; C09G 1/06 Primary Examiner-Theodore Morris (52) U.S. C. ........................................... 106/3; 106/10 57 ABSTRACT 58) Field of Search ............................. 106/3; 252/106 A tarnish remover/metal polish formulation comprising 56 References Cited water, an acid, and metal iodide, such as potassium U.S. PATENT DOCUMENTS iodide, is described. The components of the formulation chemically react with the tarnish or stain on a metal 840,167 1/1907 Springborn et al. .................... 106/6 1,280,939 0/1918 Allen ................ ... 06/3 surface, removing the tarnish or stain while leaving the 1,737,222 11/1929 Dewey, Jr. ... 106/9 metal unaffected. -
Copper Alloys
THE COPPER ADVANTAGE A Guide to Working With Copper and Copper Alloys www.antimicrobialcopper.com CONTENTS I. Introduction ............................. 3 PREFACE Conductivity .....................................4 Strength ..........................................4 The information in this guide includes an overview of the well- Formability ......................................4 known physical, mechanical and chemical properties of copper, Joining ...........................................4 as well as more recent scientific findings that show copper has Corrosion ........................................4 an intrinsic antimicrobial property. Working and finishing Copper is Antimicrobial ....................... 4 techniques, alloy families, coloration and other attributes are addressed, illustrating that copper and its alloys are so Color ..............................................5 adaptable that they can be used in a multitude of applications Copper Alloy Families .......................... 5 in almost every industry, from door handles to electrical circuitry to heat exchangers. II. Physical Properties ..................... 8 Copper’s malleability, machinability and conductivity have Properties ....................................... 8 made it a longtime favorite metal of manufacturers and Electrical & Thermal Conductivity ........... 8 engineers, but it is its antimicrobial property that will extend that popularity into the future. This guide describes that property and illustrates how it can benefit everything from III. Mechanical -
The Care and Preservation of Historical Silver by CLARA DECK, CONSERVATOR REVISIONS by LOUISE BECK, CONSERVATOR
The Care and Preservation of Historical Silver BY CLARA DECK, CONSERVATOR REVISIONS BY LOUISE BECK, CONSERVATOR Introduction Historical silver can be maintained for years of use and enjoyment provided that some basic care and attention is given to their preservation. The conservation staff at The Henry Ford have compiled the information in this fact sheet to help individuals care for their objects and collections. The first step in the care of all collections is to understand and minimize or eliminate conditions that can cause damage. The second step is to follow basic guidelines for care, handling and cleaning. Most people know that silver is a white, lustrous metal. Pure or “fine” silver is called “Sterling” if it is made up of no less than 925 parts silver to 75 parts alloy. Sterling will thus often have ‘.925’ stamped somewhere on it, as an identifier. Silver objects, especially coins and jewelry, contain copper as an alloying metal for added hardness. The copper may corrode to form dark brown or green deposits on the surface of the metal. Silver is usually easy to differentiate from lead or pewter, which are generally dark gray and not very shiny. Silver is often plated (deposited) onto other metallic alloys, almost always with an intermediate layer of copper in between. The earliest plating process, “Sheffield Plate” was developed in England in 1742. By the mid-19th century, the process was largely replaced by electroplating (which used less silver). The base metal in plated artifacts may consist of any of the following metals or alloys: copper, brass, “German silver” or “nickel silver” (50% copper, 30% nickel, 20% zinc), “Brittania metal” (97% tin, 7% antimony, 2% copper), or a “base” silver containing a high percentage of copper. -
A Thesis for the Degree of Doctor of Philosophy The
A THESIS FOR THE DEGREE OF DOCTOR OF PHILOSOPHY THE THERMAL DEGRADATION OF SOME POLYELECTROLYTES BY MUHAMMAD ZULFIQAR A SUPERVISOR: DR. I.C. McNEILL Chemistry Department, University of Glasgow. October, 1975. ProQuest Number: 13803963 All rights reserved INFORMATION TO ALL USERS The quality of this reproduction is dependent upon the quality of the copy submitted. In the unlikely event that the author did not send a complete manuscript and there are missing pages, these will be noted. Also, if material had to be removed, a note will indicate the deletion. uest ProQuest 13803963 Published by ProQuest LLC(2018). Copyright of the Dissertation is held by the Author. All rights reserved. This work is protected against unauthorized copying under Title 17, United States Code Microform Edition © ProQuest LLC. ProQuest LLC. 789 East Eisenhower Parkway P.O. Box 1346 Ann Arbor, Ml 4 8 1 0 6 - 1346 PREFACE The work described in this thesis was carried out during the period October 1971 to September 1974 at the University of Glasgow, in the Department of Physical Chemistry, which is under the supervision of Professor G.A. Sim. My thanks are due to my colleagues in the Macromolecular Chemistry group for invaluable assistance and discussion, and to various members of the technical staff of the Chemistry Department, in particular, Mr. J. Gorman and Mrs. F. Lawrie. Finally, I should like to thank my supervisor, Dr. I«C. McNeill, for suggesting the topic of this thesis, and for his advice and constant .encouragement throughout this work. SUMMARY All naturally occurring polyelectrolytes are found in an aqueous environment and this feature directed most of the chemical research in this field towards an understanding of polyelectrolyte behaviour in aqueous solution. -
A Study of Nickel Molybdenum Oxide Catalysts for The
A STUDY OF NICKEL MOLYBDENUM OXIDE CATALYSTS FOR THE OXIDATIVE DEHYDROGENATION OF n-HEXANE By Bavani Pillay Submitted in fulfilment of the academic requirements for the degree of Doctor of Philosophy in the School of Chemistry University of KwaZulu-Natal Durban, South Africa June 2009 As the candidate’s supervisor I have/have not approved this thesis/dissertation for submission. Signed: _____________ Name: _____________ Date: ______________ ii ABSTRACT Nickel molybdenum oxide catalysts with different chemical compositions have been synthesized and tested for the oxidative dehydrogenation of n-hexane. The co-precipitation method was used for the synthesis and several methods were used to characterize these catalysts. These include inductively-coupled plasma optical emission spectroscopy, Raman spectroscopy, infrared spectroscopy, energy dispersive X-ray spectroscopy, scanning electron microscopy, temperature programmed reduction, temperature programmed desorption, X-ray photo-electron spectroscopy and X-ray diffraction spectroscopy techniques as well as the Brauner-Emmet-Teller technique for surface area determination. The phase composition of the catalysts was largely dependent on the chemical composition. Catalyst testing on n-hexane feed was done with a fixed bed continuous flow reactor and experiments were performed with feed/air ratios above and below the flammability limit. Varied reaction conditions were used for the catalytic testing. Prior to the catalytic testing, blank experiments were performed. Analysis of the products were done both online and offline in conjunction with gas chromatography employing FID and TCD detectors. The influence of the catalyst on the conversion of n-hexane and selectivity to dehydrogenation products is reported. Products observed were the carbon oxides (CO and CO 2), isomers of hexene (1-hexene, 2-hexene and 3-hexene), cyclic C 6 products (cyclohexene and benzene), cracked products: alkanes/alkenes (propane/ene, butane/ene) and oxygenates (ethanal, acetic acid and propanoic acid). -
H2S Pollution and Its Effect on Corrosion of Electronic Components
Chapter 13 H2S Pollution and Its Effect on Corrosion of Electronic Components Benjamin Valdez Salas, Michael Schorr Wiener, Gustavo Lopez Badilla, Monica Carrillo Beltran, Roumen Zlatev, Margarita Stoycheva, Juan de Dios Ocampo Diaz, Lidia Vargas Osuna and Juan Terrazas Gaynor Additional information is available at the end of the chapter http://dx.doi.org/10.5772/39247 1. Introduction The microelectronic industry applies materials with good electrical and corrosion resistance properties for the manufacturing of the microelectronic devices. Silver and copper are materials with this characteristics used for that purpose. Some of their main applications are as high thermal conductive die attach paste that had silver flakes as conductive filler material, silver plated over copper frames, Sn-Ag and Sn-Cu alloys for solder paste used in Surface Mount Technology (SMT) process, conductive internal copper layers in printed circuit boards, copper wire bonding, and more. Other metals and alloys, widely used for support frames, heat diffusers and case wares in the electronics industry are tin, nickel, aluminum, carbon steel and galvanized steel. Corrosion in microelectronics depends on several variants such as the package type, materials involved, assembly processes, moisture, inorganic and organic contaminants, atmospheric pollutants, temperature, thermal stress and electrical bias.(P. Roberge, 2000, J. Payer, 1990, M.Reid et al., 2007, M. Tullmin and P. Roberge, 1995, M. McNeil and B. Little, 1992, X. Lin and J. Zhang, 2004) The plastic packages are the more widely used because of its size, cost and manufacturability advantages but, compared to other hermetic package systems like ceramics, are non-hermetic due to its polymeric materials that permit the permeation of moisture and corrosive gases, allowing in this manner the appearance of other problems associated with corrosion of the inside components. -
Chemical Formula of Binary Ionic Compounds – Sheet 1 the Combining Power Or Valency of Silver Is Always 1
Chemical Formula of Binary Ionic Compounds – Sheet 1 The combining power or valency of silver is always 1. All other transition metals are 2 unless otherwise indicated. No. Binary compound Formula No. Binary compound Formula 1 potassium fluoride 26 calcium sulfide 2 calcium chloride 27 lithium bromide 3 barium bromide 28 nickel sulfide 4 silver sulfide 29 zinc phosphide 5 aluminium iodide 30 barium iodide 6 potassium iodide 31 caesium chloride 7 lead(IV) oxide 32 copper bromide 8 zinc nitride 33 sodium nitride 9 silver iodide 34 silver chloride 10 barium fluoride 35 sodium hydride 11 lead(II) iodide 36 potassium nitride 12 silver fluoride 37 cobalt chloride 13 sodium sulfide 38 magnesium sulfide 14 sodium bromide 39 potassium chloride 15 calcium oxide 40 calcium bromide 16 zinc fluoride 41 iron(III) oxide 17 strontium phosphide 42 aluminium fluoride 18 barium sulfide 43 magnesium bromide 19 aluminium oxide 44 iron(III) chloride 20 aluminium chloride 45 barium nitride 21 aluminium sulfide 46 sodium fluoride 22 lead(II) oxide 47 lithium fluoride 23 barium chloride 48 lithium iodide 24 copper chloride 49 lithium hydride 25 barium phosphide 50 potassium oxide “Aluminum” and “cesium” are commonly used alternative spellings for "aluminium" and "caesium that are used in the US. May be freely copied for educational use. ©www.chemicalformula.org Chemical Formula of Binary Ionic Compounds – Sheet 2 The combining power or valency of silver is always 1. All other transition metals are 2 unless otherwise indicated. No. Binary compound Formula No. -
DECORATIVE CHROMIUM PLATING I=O44-5 by Donald L
DECORATIVE CHROMIUM PLATING I=o44-5 by Donald L. Snyder 2$& f Engelhard Corp., Beachwood, OH 13lcctrotlcposition of chromium is thc principii1 tncitns of iiiip:trting thc physicill itntl clicniical propcrtics ol’chromium 10 thc surface of lcss cxpcnsive antl casier to lbrm matcriiils such as steel and plastics. The most desirable properties of chromium as a metal coating are its inherent protective and decorative characteristics. The deposit’s high reflectively is retained in service because of chromium’s excellent tarnish, corrosion, wear and scratch resistance. Chromium is almost exclusively plated over a nickel electrodeposit which can easily be plated over substrates such as plastics, steel, aluminum, copper alloys, and zinc die castings. Nickel is preferred because it protects the substrate from corrosion, helps give chromium a white color, and is protected from surface oxidation by the chromium. Stainless steel is the only substrate that is frequently plated directly with chromium, but a nickel preplate before chromium is also used. Multiple or single layers of nickel and copper can precede the nickel/chromium deposits depending upon the intended use of the part. Decorative chromium deposits typically are plated in the 2 to 20 millionths of an inch range. Thicker deposits tend to be duller and contain visible cracks. The traditional chromium deposit is produced from an electroplating electrolyte contain- ing hexavalent chromium ions and has a pleasing bluish-white decorative appearance. About 1975, a chromium electrolyte containing the less toxic and less hazardous trivalent chromium ion began replacing many decorative hexavalent chromium electroplating installations. De- pending upon the process, trivalent chromium electrolytes can either produce a metallic white deposit almost identical in appearance to the bluish-white hexavalent chromium deposits or a deep looking pewter or stainless steel appearing deposit. -
Team Metal Finishing Inc
Team Metal Finishing Inc. Available Processes: Anodizing Thank you for considering Team Metal Finishing for your Hard Coating processing requirements. Team Metal Finishing has been in Electroless Nickel business since 1988 serving the Aerospace, Automotive, Military, Sulfamate Nickel Electronics, Motion Controls and Medical Industries. Since our Bright and Matte Nickel founding we have developed a stellar reputation within these Silver Plating industries for meeting and exceeding the needs and requirements Gold Plating of our customers. We are a ISO 9001:2015 certified company Tin Plating with Aerospace accreditations. We have more than 60,000 Chromate Conversion Coating square feet of processing area on 7.6 acres located in Eastanollee Immersion Tin Ga. Passivation Electropolishing Please give us a call to see what our Team can do for you. www.teammetalfinishing.com 1-800-380-3371 [email protected] Process List: Anodizing Clear & Colors: Black, Blue, Red, Orange and Gold Hard Coat Clear or Natural, Colors: Black, Blue, Red, Orange and Gold Electroless Nickel Medium and High phosphorus; Black Electroless Nickel Nickel Plating Sulfamate, Bright, Matte, and Satin Silver Plating Matte, Semi Bright and Bright Gold Plating 24K Tin Plating Bright and Immersion Tin Chromate Conversions on Aluminum Color: Clear. Trivalent, RoHs. Passivation and Electropolishing Stainless Steels only Abrasive Blasting Glass bead blasting Baking Hydrogen Embrittlement relief Teflon Bonded used with all our coatings www.teammetalfinishing.com 1-800-380-3371 [email protected] Anodizing: Anodizing is an electrolytic process that forms an aluminum oxide onto the surface of the material. The oxide film that is formed grows from the base metal as an integral part of the material. -
Release of Fission Products During and After Oxidation of Trace-Irradiated Uranium Dioxide at 3Oo-9Oo°C
XA0056017 RELEASE OF FISSION PRODUCTS DURING AND AFTER OXIDATION OF TRACE-IRRADIATED URANIUM DIOXIDE AT 3OO-9OO°C P. Wood, G.H. Bannister Central Electricity Generating Board Berkeley Nuclear Laboratories UK Abstract Should defected U02 fuel pins come into contact with air then oxidation of the fuel may occur, the rate and consequences of which are dependent upon temperature and oxygen partial pressure. At CEGB-BNL an experimental programme is underway investigating the kinetics, and extent, of release of fission products during and after oxidation of trace-irradiated U02 to U3O3, and reduction of U3O3 to UO 2« This paper presents preliminary results and analysis of experiments performed at 300-900°C. Dense sintered U02 has been oxidised at 300-500°C using a thermobalance with simultaneous counting of released 85Kr. The kinetics of the 35Kr release are shown to correlate with the kinetics of oxidation, and the extent of release has been determined as 3-8% of that in the UO 2 converted to U3O3. The release of 106Ru and 137Cs during this oxidation has been estimated by Y~c°unting of the fuel sample, before and after oxidation, and of glassware in the vicinity of the sample. This indicates slight release of ruthenium and caesium. Greater fission product release is caused by oxidation at higher temperatures or by heating of the oxidation product. U 308 produced at 400°C has been heated at 800 and 900°C in air for 20 hours. This results in near total release of 85Kr and 106Ru, but still only slight release of 137Cs.