TOPIC 3. IONIC COMPOUNDS: Formation, Formulas and Naming
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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. -
Material Safety Data Sheet
LTS Research Laboratories, Inc. Safety Data Sheet Calcium Selenide ––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––– 1. Product and Company Identification ––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––– Trade Name: Calcium Selenide Chemical Formula: CaSe Recommended Use: Scientific research and development Manufacturer/Supplier: LTS Research Laboratories, Inc. Street: 37 Ramland Road City: Orangeburg State: New York Zip Code: 10962 Country: USA Tel #: 855-587-2436 / 855-lts-chem 24-Hour Emergency Contact: 800-424-9300 (US & Canada) +1-703-527-3887 (International) ––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––– 2. Hazards Identification ––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––– Signal Word: Danger Hazard Statements: H301+H331: Toxic if swallowed or if inhaled H373: May cause damage to organs through prolonged or repeated exposure H400: Very toxic to aquatic life H410: Very toxic to aquatic life with long lasting effects Precautionary Statements: P260: Do not breathe dust/fume/gas/mist/vapours/spray P261: Avoid breathing dust/fume/gas/mist/vapours/spray P264: Wash thoroughly after handling P270: Do not eat, drink or smoke when using this product P271: Use only outdoors or in a well-ventilated area P273: Avoid release to the environment P301+P310: IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician P304+P341: IF INHALED: If breathing is difficult, -
Chemistry Workbook
Bridging the gap 2020 Ripon Grammar School 1 2 Introduction Advanced level Chemistry is a demanding and exciting course. In order to be prepared for your start in September a number of areas from GCSE chemistry are needed to be ‘known’ thoroughly. To help you make the transition as smoothly as possible we have put together this series of exercises. When you start in September you will be expected to have completed the exercises within this booklet and know the material within. It is by no means ALL you need to know but the very foundations of the exciting journey you are about to start. If you have difficulties or confusions there are a number of suggested online resources you could try. There will be opportunities to discuss concerns with staff at the beginning of the year but you should have made significant headway independently. This booklet contains some notes to act as a reminder. If you struggle with a particular area you should investigate the suggested support resources including your GCSE notes. There are exercises for you to complete, the answers are at the end. Contents Periodic Table 2 Topics Writing formulae 4 Equations 7 Moles 10 Atomic Structure 15 Identifying Bonding and Structure types 19 Answers to exercises 20 3 Writing formulae Objectives: • Know the common ions • Be able to construct formulae for common ionic substances • Know the formulae of some common covalent substances Common Ions (you need to know these): Putting together an ionic formula: The charges must balance. Molecular ions will need to be contained in brackets. -
US2278550.Pdf
April 7, 1942. D. J. OER E. A. 2,278,550 PREPARATION OF ALKALI METAL ALKOXIDES Filed June 21, 1939 REACTION ------ REGENERATION OFMX FROM M-represents an alkali metal N-represents a number from 2 to 3 R-represents an alkyl group X-represents the anion of a weak acid Donald D. Lee Donald J. Loder NVENTOR BY 232 az - ATTORNEY Patented Apr. 7, 1942 2,278,550 UNITED STATES PATENT OFFICE 2,278,550 PREPARATION OF ALKALI METAL ALKOXDES Donald J. Loder and Donald D. Lee, Wilmington, Del, assignors to E. I. du Pont de Nemours & Company, Wilmington, Del., a corporation of Delaware Application June 21, 1939, Serial No. 280,308 16 Claims. (CI. 260-632) The invention relates to improvements in the and R is an alkyl, or aralkyl radical which may be manufacture of metal alkoxides and more particu Saturated, unsaturated, substituted or unsub larly to the preparation of alkali metal alkoxides stituted. by the interaction of alcohols with alkali metal In Reactions 1 and 2, an alkali metal salt of a salts of weak acids. weak acid is digested with an alcohol at an ap Alkali metal alkoxides have been prepared by propriate temperature, the digestion being Con. direct reaction of the alkali metal as such with tinued until equilibrium has been substantially an alcohol. or by action of an alkali metal hy reached. The equilibrium mixture is filtered for. droxide. upon an alcohol. The higher cost of the the separation of any undissolved (MX or M3X) first of these methods has limited somewhat the O salt and the resulting solution (or filtrate) is industrial use of the alkoxide thus prepared and found to contain an alkali metal alkoxide, or much effort has been expended in endeavors to aralkoxide, (MOR) hereinafter called 'al make the second more commercially practicable. -
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. -
High Purity Inorganics
High Purity Inorganics www.alfa.com INCLUDING: • Puratronic® High Purity Inorganics • Ultra Dry Anhydrous Materials • REacton® Rare Earth Products www.alfa.com Where Science Meets Service High Purity Inorganics from Alfa Aesar Known worldwide as a leading manufacturer of high purity inorganic compounds, Alfa Aesar produces thousands of distinct materials to exacting standards for research, development and production applications. Custom production and packaging services are part of our regular offering. Our brands are recognized for purity and quality and are backed up by technical and sales teams dedicated to providing the best service. This catalog contains only a selection of our wide range of high purity inorganic materials. Many more products from our full range of over 46,000 items are available in our main catalog or online at www.alfa.com. APPLICATION FOR INORGANICS High Purity Products for Crystal Growth Typically, materials are manufactured to 99.995+% purity levels (metals basis). All materials are manufactured to have suitably low chloride, nitrate, sulfate and water content. Products include: • Lutetium(III) oxide • Niobium(V) oxide • Potassium carbonate • Sodium fluoride • Thulium(III) oxide • Tungsten(VI) oxide About Us GLOBAL INVENTORY The majority of our high purity inorganic compounds and related products are available in research and development quantities from stock. We also supply most products from stock in semi-bulk or bulk quantities. Many are in regular production and are available in bulk for next day shipment. Our experience in manufacturing, sourcing and handling a wide range of products enables us to respond quickly and efficiently to your needs. CUSTOM SYNTHESIS We offer flexible custom manufacturing services with the assurance of quality and confidentiality. -
Light-Assisted Delithiation of Lithium Iron Phosphate Nanocrystals Towards Photo-Rechargeable Lithium Ion Batteries
ARTICLE Received 7 Nov 2016 | Accepted 17 Jan 2017 | Published 10 Apr 2017 DOI: 10.1038/ncomms14643 OPEN Light-assisted delithiation of lithium iron phosphate nanocrystals towards photo-rechargeable lithium ion batteries Andrea Paolella1,2, Cyril Faure1, Giovanni Bertoni3, Sergio Marras4, Abdelbast Guerfi1, Ali Darwiche1, Pierre Hovington1, Basile Commarieu1, Zhuoran Wang2, Mirko Prato4, Massimo Colombo4, Simone Monaco4, Wen Zhu1, Zimin Feng1, Ashok Vijh1, Chandramohan George5, George P. Demopoulos2, Michel Armand6 & Karim Zaghib1 Recently, intensive efforts are dedicated to convert and store the solar energy in a single device. Herein, dye-synthesized solar cell technology is combined with lithium-ion materials to investigate light-assisted battery charging. In particular we report the direct photo- oxidation of lithium iron phosphate nanocrystals in the presence of a dye as a hybrid photo-cathode in a two-electrode system, with lithium metal as anode and lithium hexafluorophosphate in carbonate-based electrolyte; a configuration corresponding to lithium ion battery charging. Dye-sensitization generates electron–hole pairs with the holes aiding the delithiation of lithium iron phosphate at the cathode and electrons utilized in the formation of a solid electrolyte interface at the anode via oxygen reduction. Lithium iron phosphate acts effectively as a reversible redox agent for the regeneration of the dye. Our findings provide possibilities in advancing the design principles for photo-rechargeable lithium ion batteries. 1 Institute de Recherche d-Hydro-Que´bec (IREQ), 1800 Boulevard Lionel Boulet, Varennes, Quebec, Canada J3X 1S1. 2 Department of Mining and Materials Engineering, McGill University, Wong Building, 3610 University Street, Montreal, Quebec, Canada H3A OC5. 3 IMEM-CNR, Parco Area delle Scienze 37/A, 43124 Parma, Italy. -
List of Lists
United States Office of Solid Waste EPA 550-B-10-001 Environmental Protection and Emergency Response May 2010 Agency www.epa.gov/emergencies LIST OF LISTS Consolidated List of Chemicals Subject to the Emergency Planning and Community Right- To-Know Act (EPCRA), Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) and Section 112(r) of the Clean Air Act • EPCRA Section 302 Extremely Hazardous Substances • CERCLA Hazardous Substances • EPCRA Section 313 Toxic Chemicals • CAA 112(r) Regulated Chemicals For Accidental Release Prevention Office of Emergency Management This page intentionally left blank. TABLE OF CONTENTS Page Introduction................................................................................................................................................ i List of Lists – Conslidated List of Chemicals (by CAS #) Subject to the Emergency Planning and Community Right-to-Know Act (EPCRA), Comprehensive Environmental Response, Compensation and Liability Act (CERCLA) and Section 112(r) of the Clean Air Act ................................................. 1 Appendix A: Alphabetical Listing of Consolidated List ..................................................................... A-1 Appendix B: Radionuclides Listed Under CERCLA .......................................................................... B-1 Appendix C: RCRA Waste Streams and Unlisted Hazardous Wastes................................................ C-1 This page intentionally left blank. LIST OF LISTS Consolidated List of Chemicals -
Reactions of Liquid Hydrogen Sulfide on Metals and Oxides Sitaram D
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1928 Reactions of liquid hydrogen sulfide on metals and oxides Sitaram D. Satwalekar Iowa State College Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Inorganic Chemistry Commons Recommended Citation Satwalekar, Sitaram D., "Reactions of liquid hydrogen sulfide on metals and oxides " (1928). Retrospective Theses and Dissertations. 14290. https://lib.dr.iastate.edu/rtd/14290 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. INFORMATION TO USERS This manuscript has been reproduced from the microfilm master. UMI films the text directly from the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter face, while others may be from any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are reproduced by sectioning the original, beginning at the upper left-hand corner and continuing from left to right in equal sections with small overlaps. -
Chemical Names and CAS Numbers Final
Chemical Abstract Chemical Formula Chemical Name Service (CAS) Number C3H8O 1‐propanol C4H7BrO2 2‐bromobutyric acid 80‐58‐0 GeH3COOH 2‐germaacetic acid C4H10 2‐methylpropane 75‐28‐5 C3H8O 2‐propanol 67‐63‐0 C6H10O3 4‐acetylbutyric acid 448671 C4H7BrO2 4‐bromobutyric acid 2623‐87‐2 CH3CHO acetaldehyde CH3CONH2 acetamide C8H9NO2 acetaminophen 103‐90‐2 − C2H3O2 acetate ion − CH3COO acetate ion C2H4O2 acetic acid 64‐19‐7 CH3COOH acetic acid (CH3)2CO acetone CH3COCl acetyl chloride C2H2 acetylene 74‐86‐2 HCCH acetylene C9H8O4 acetylsalicylic acid 50‐78‐2 H2C(CH)CN acrylonitrile C3H7NO2 Ala C3H7NO2 alanine 56‐41‐7 NaAlSi3O3 albite AlSb aluminium antimonide 25152‐52‐7 AlAs aluminium arsenide 22831‐42‐1 AlBO2 aluminium borate 61279‐70‐7 AlBO aluminium boron oxide 12041‐48‐4 AlBr3 aluminium bromide 7727‐15‐3 AlBr3•6H2O aluminium bromide hexahydrate 2149397 AlCl4Cs aluminium caesium tetrachloride 17992‐03‐9 AlCl3 aluminium chloride (anhydrous) 7446‐70‐0 AlCl3•6H2O aluminium chloride hexahydrate 7784‐13‐6 AlClO aluminium chloride oxide 13596‐11‐7 AlB2 aluminium diboride 12041‐50‐8 AlF2 aluminium difluoride 13569‐23‐8 AlF2O aluminium difluoride oxide 38344‐66‐0 AlB12 aluminium dodecaboride 12041‐54‐2 Al2F6 aluminium fluoride 17949‐86‐9 AlF3 aluminium fluoride 7784‐18‐1 Al(CHO2)3 aluminium formate 7360‐53‐4 1 of 75 Chemical Abstract Chemical Formula Chemical Name Service (CAS) Number Al(OH)3 aluminium hydroxide 21645‐51‐2 Al2I6 aluminium iodide 18898‐35‐6 AlI3 aluminium iodide 7784‐23‐8 AlBr aluminium monobromide 22359‐97‐3 AlCl aluminium monochloride -
Mass Balance and Trapping of Headspace Samples Of
MASS BALANCE AND TRAPPING OF HEADSPACE SAMPLES OF BIOREMEDIATION IN SELENIUM AMENDED SAMPLES ________________________________ A THESIS PRESENTED TO THE FACULTY OF THE DEPARTMENT OF CHEMISTRY SAM HOUSTON STATE UNIVERSITY ________________________________ IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE ________________________________ BY SUMINDA HAPUARACHCHI AUGUST, 2002 2 MASS BALANCE AND TRAPPING OF HEADSPACE SAMPLES OF BIOREMEDIATION IN SELENIUM AMENDED SAMPLES BY SUMINDA HAPUARACHCHI APPROVED: ________________________________ THOMAS G. CHASTEEN, THESIS DIRECTOR ________________________________ BENNY E. ARNEY JR. ________________________________ Mike McCann APPROVED: ________________________________ Dr. Brian Chapman, Dean College of Arts and Sciences 3 ABSTRACT Hapuarachchi, Suminda, Mass balance and trapping of headspace samples of bioremediation in selenium amended samples, Master of Science (Chemistry), August 2002, Sam Houston State University, Huntsville, Texas. One of the purposes of these experiments was to determine the mass balance in the bioremediation of selenium amended samples and to try to improve the efficiency of the bioremediation of selenium. The other purpose was to study the interference of glass containers in selenium determination by atomic absorption spectrometry with hydride generation. In this research, the first step was to develop a gas phase trapping method and to prove the success of that method using known concentrations of known organo-selenium compounds. Fifty percent nitric solution was a good trapping solution to collect volatile organoselenium compounds purged from live, liquid bacterial cultures. Then, bioreactor experiments were carried out to determine the mass balance of selenium as it was biologically processed by a selenium-resistant bacterium. First, bioreactor experiments were undertaken anaerobically with different amended selenium concentrations and the mass balance of each process measured. -
UNITED STATES PATENT OFFICE METHOD of MAKING CERYSTALLINE ALU 'MINASAME and a PRODUCT CONTAINING the Raymond R
Reissued Nov. 2, 1937 Re.20,547 UNITED STATES PATENT OFFICE METHOD OF MAKING CERYSTALLINE ALU 'MINASAME AND A PRODUCT CONTAINING THE Raymond R. Ridgway, Niagara Falls, N. Y., as signor to Norton Company, Worcester, Mass, a corporation of Massachusetts No Drawing. Original No. 2,003,867, dated June 4, 1935, Serial No. 690,589, September 22, 1933. Application for reissue January 8, 1936, Serial No. 58,235 31 Claims. (CI, 23-142) This invention relates to the electrochemical remove impurities, but such products must there manufacture of crystalline alumina of required after be re-fused in order that the purifled crys chemical and given physical properties for use in talline alumina may have the desired physical as various industrial arts. -- well as chemical characteristics. These alterna 5. In the electrometallurgical production of crys tive methods, which involve over-purification and talline alumina from alumina-containing Ores, reduction of some of the alumina in the original such as bauxite, the elimination of the impuri furnacing of bauxite, have not produced in prac ties of the ore by reduction with carbon has had tice the desired results, since the oxidizing agents serious limitations, from the standpoint of pu have remained as contaminations in the final 10 rity and stability of the resultant alumina crys product, or else the reactions have been incon- 0 tals. Commercial bauxite contains as high as plete. Moreover, those processes which involve 4% of titania, and 2% of zirconia, as well as sil an intermediate purification and a subsequent ica and alkaline metal oxides. It has been cus second fusion of the material are expensive anti tomary to purify the alumina oxide incomplete involve great technical difficulties.