Acetylene (Dissolved)

Total Page:16

File Type:pdf, Size:1020Kb

Acetylene (Dissolved) ACETYLENE (DISSOLVED) A-Gas South Africa Chemwatch Hazard Alert Code: 4 Chemwatch: 1001 Issue Date: 16/10/2014 Version No: 5.1.1.1 Print Date: 16/08/2018 Safety Data Sheet (Conforms to Regulaon (EU) No 2015/830) S.REACH.GBR.EN SECTION 1 IDENTIFICATION OF THE SUBSTANCE / MIXTURE AND OF THE COMPANY / UNDERTAKING 1.1. Product Idenfier Product name ACETYLENE (DISSOLVED) Chemical Name acetylene Synonyms C2H2; acetylene dissolved; ethine; ethyne; acetylen Proper shipping name ACETYLENE, DISSOLVED Chemical formula C2H2 Other means of idenficaon Not Available CAS number 74-86-2 EC number 200-816-9 Index number 601-015-00-0 REACH registraon number 01-2119457406-36-XXXX 1.2. Relevant idenfied uses of the substance or mixture and uses advised against Fuel gas for oxy-acetylene welding, flame cung, gouging, metal scale removal, brazing, flame hardening and general localised heang. Burnt Relevant idenfied uses with oxygen as illuminant in navigaonal beacons. Used as a source of carbon black and as reactant in manufacture of vinyl chloride, acrylates etc. Uses advised against Not Applicable 1.3. Details of the supplier of the safety data sheet Registered company name A-Gas South Africa Address 8 Railway Road Montague Gardens 7441 Cape Town South Africa Telephone +27 0 21 551 8790 Fax +27 0 21 551 8758 Website Not Available Email Not Available 1.4. Emergency telephone number Associaon / Organisaon Not Available Emergency telephone Not Available numbers Other emergency telephone Not Available numbers SECTION 2 HAZARDS IDENTIFICATION 2.1. Classificaon of the substance or mixture Classificaon according to regulaon (EC) No 1272/2008 H220 - Flammable Gas Category 1, H280 - Gas under Pressure [CLP] [2] Legend: 1. Classified by Chemwatch; 2. Classificaon drawn from Regulaon (EU) No 1272/2008 - Annex VI 2.2. Label elements Hazard pictogram(s) SIGNAL WORD DANGER Hazard statement(s) H220 Extremely flammable gas. H280 Contains gas under pressure; may explode if heated. Supplementary statement(s) EUH006 Explosive with or without contact with air. Precauonary statement(s) Prevenon P210 Keep away from heat, hot surfaces, sparks, open flames and other ignion sources. No smoking. Precauonary statement(s) Response P377 Leaking gas fire: Do not exnguish, unless leak can be stopped safely. P381 In case of leakage, eliminate all ignion sources. Precauonary statement(s) Storage P403 Store in a well-venlated place. Precauonary statement(s) Disposal Not Applicable 2.3. Other hazards Inhalaon and/or ingeson may produce health damage*. May produce discomfort of the respiratory system*. Repeated exposure potenally causes skin dryness and cracking*. Vapours potenally cause drowsiness and dizziness*. Acetylene (Dissolved) Listed in the Europe Regulaon (EC) No 1907/2006 - Annex XVII (Label should state: "Restricted to professional users.") acetone Listed in the Europe Regulaon (EC) No 1907/2006 - Annex XVII (Label should state: "Restricted to professional users.") SECTION 3 COMPOSITION / INFORMATION ON INGREDIENTS 3.1.Substances 1.CAS No 2.EC No %[weight] Name Classificaon according to regulaon (EC) No 1272/2008 [CLP] 3.Index No 4.REACH No 1.74-86-2 2.200-816-9 98-99 Acetylene (Dissolved) Flammable Gas Category 1, Gas under Pressure; H220, H280, EUH006 [2] 3.601-015-00-0 4.01-2119457406-36-XXXX dissolved in 1.67-64-1 2.200-662-2 Flammable Liquid Category 2, Specific target organ toxicity - single exposure Category 3 acetone * 3.606-001-00-8 (narcoc effects), Eye Irritaon Category 2; H225, H336, H319, EUH066 [2] 4.01-2119471330-49-XXXX * instrument grade acetylene is specially purified. Legend: 1. Classified by Chemwatch; 2. Classificaon drawn from Regulaon (EU) No 1272/2008 - Annex VI; 3. Classificaon drawn from C&L; * EU IOELVs available 3.2.Mixtures See 'Informaon on ingredients' in secon 3.1 SECTION 4 FIRST AID MEASURES 4.1. Descripon of first aid measures If product comes in contact with eyes remove the paent from gas source or contaminated area. Take the paent to the nearest eye wash, shower or other source of clean water. Eye Contact Open the eyelid(s) wide to allow the material to evaporate. Gently rinse the affected eye(s) with clean, cool water for at least 15 minutes. Have the paent lie or sit down and lt the head back. Hold the eyelid(s) open and pour water slowly over the eyeball(s) at the inner corners, leng the water run out of the outer corners. The paent may be in great pain and wish to keep the eyes closed. It is important that the material is rinsed from the eyes to prevent further damage. Ensure that the paent looks up, and side to side as the eye is rinsed in order to beer reach all parts of the eye(s) Transport to hospital or doctor. Even when no pain persists and vision is good, a doctor should examine the eye as delayed damage may occur. If the paent cannot tolerate light, protect the eyes with a clean, loosely ed bandage. Ensure verbal communicaon and physical contact with the paent. DO NOT allow the paent to rub the eyes DO NOT allow the paent to ghtly shut the eyes DO NOT introduce oil or ointment into the eye(s) without medical advice DO NOT use hot or tepid water. If skin or hair contact occurs: Skin Contact Flush skin and hair with running water (and soap if available). Seek medical aenon in event of irritaon. Following exposure to gas, remove the paent from the gas source or contaminated area. NOTE: Personal Protecve Equipment (PPE), including posive pressure self-contained breathing apparatus may be required to assure the safety of the rescuer. Prostheses such as false teeth, which may block the airway, should be removed, where possible, prior to iniang first aid procedures. If the paent is not breathing spontaneously, administer rescue breathing. If the paent does not have a pulse, administer CPR. Inhalaon If medical oxygen and appropriately trained personnel are available, administer 100% oxygen. Summon an emergency ambulance. If an ambulance is not available, contact a physician, hospital, or Poison Control Centre for further instrucon. Keep the paent warm, comfortable and at rest while awaing medical care. MONITOR THE BREATHING AND PULSE, CONTINUOUSLY. Administer rescue breathing (preferably with a demand-valve resuscitator, bag-valve mask-device, or pocket mask as trained) or CPR if necessary. Avoid giving milk or oils. Avoid giving alcohol. Ingeson Not considered a normal route of entry. If spontaneous voming appears imminent or occurs, hold paent's head down, lower than their hips to help avoid possible aspiraon of vomitus. 4.2 Most important symptoms and effects, both acute and delayed See Secon 11 4.3. Indicaon of any immediate medical aenon and special treatment needed For acute or short term repeated exposures to petroleum disllates or related hydrocarbons: Primary threat to life, from pure petroleum disllate ingeson and/or inhalaon, is respiratory failure. Paents should be quickly evaluated for signs of respiratory distress (e.g. cyanosis, tachypnoea, intercostal retracon, obtundaon) and given oxygen. Paents with inadequate dal volumes or poor arterial blood gases (pO2 50 mm Hg) should be intubated. Arrhythmias complicate some hydrocarbon ingeson and/or inhalaon and electrocardiographic evidence of myocardial injury has been reported; intravenous lines and cardiac monitors should be established in obviously symptomac paents. The lungs excrete inhaled solvents, so that hypervenlaon improves clearance. A chest x-ray should be taken immediately aer stabilisaon of breathing and circulaon to document aspiraon and detect the presence of pneumothorax. Epinephrine (adrenalin) is not recommended for treatment of bronchospasm because of potenal myocardial sensisaon to catecholamines. Inhaled cardioselecve bronchodilators (e.g. Alupent, Salbutamol) are the preferred agents, with aminophylline a second choice. Lavage is indicated in paents who require decontaminaon; ensure use of cuffed endotracheal tube in adult paents. [Ellenhorn and Barceloux: Medical Toxicology] For gas exposures: -------------------------------------------------------------- BASIC TREATMENT -------------------------------------------------------------- Establish a patent airway with sucon where necessary. Watch for signs of respiratory insufficiency and assist venlaon as necessary. Administer oxygen by non-rebreather mask at 10 to 15 l/min. Monitor and treat, where necessary, for pulmonary oedema . Monitor and treat, where necessary, for shock. Ancipate seizures. -------------------------------------------------------------- ADVANCED TREATMENT -------------------------------------------------------------- Consider orotracheal or nasotracheal intubaon for airway control in unconscious paent or where respiratory arrest has occurred. Posive-pressure venlaon using a bag-valve mask might be of use. Monitor and treat, where necessary, for arrhythmias. Start an IV D5W TKO. If signs of hypovolaemia are present use lactated Ringers soluon. Fluid overload might create complicaons. Drug therapy should be considered for pulmonary oedema. Hypotension with signs of hypovolaemia requires the cauous administraon of fluids. Fluid overload might create complicaons. Treat seizures with diazepam. Proparacaine hydrochloride should be used to assist eye irrigaon. BRONSTEIN, A.C. and CURRANCE, P.L. EMERGENCY CARE FOR HAZARDOUS MATERIALS EXPOSURE: 2nd Ed. 1994 If acetylene from a calcium carbide generator is involved, it may contain phosphine and other impuries and their acute health effects should be considered. SECTION 5 FIREFIGHTING MEASURES 5.1. Exnguishing media DO NOT EXTINGUISH BURNING GAS UNLESS LEAK CAN
Recommended publications
  • Chemical Chemical Hazard and Compatibility Information
    Chemical Chemical Hazard and Compatibility Information Acetic Acid HAZARDS & STORAGE: Corrosive and combustible liquid. Serious health hazard. Reacts with oxidizing and alkali materials. Keep above freezing point (62 degrees F) to avoid rupture of carboys and glass containers.. INCOMPATIBILITIES: 2-amino-ethanol, Acetaldehyde, Acetic anhydride, Acids, Alcohol, Amines, 2-Amino-ethanol, Ammonia, Ammonium nitrate, 5-Azidotetrazole, Bases, Bromine pentafluoride, Caustics (strong), Chlorosulfonic acid, Chromic Acid, Chromium trioxide, Chlorine trifluoride, Ethylene imine, Ethylene glycol, Ethylene diamine, Hydrogen cyanide, Hydrogen peroxide, Hydrogen sulfide, Hydroxyl compounds, Ketones, Nitric Acid, Oleum, Oxidizers (strong), P(OCN)3, Perchloric acid, Permanganates, Peroxides, Phenols, Phosphorus isocyanate, Phosphorus trichloride, Potassium hydroxide, Potassium permanganate, Potassium-tert-butoxide, Sodium hydroxide, Sodium peroxide, Sulfuric acid, n-Xylene. Acetone HAZARDS & STORAGE: Store in a cool, dry, well ventilated place. INCOMPATIBILITIES: Acids, Bromine trifluoride, Bromine, Bromoform, Carbon, Chloroform, Chromium oxide, Chromium trioxide, Chromyl chloride, Dioxygen difluoride, Fluorine oxide, Hydrogen peroxide, 2-Methyl-1,2-butadiene, NaOBr, Nitric acid, Nitrosyl chloride, Nitrosyl perchlorate, Nitryl perchlorate, NOCl, Oxidizing materials, Permonosulfuric acid, Peroxomonosulfuric acid, Potassium-tert-butoxide, Sulfur dichloride, Sulfuric acid, thio-Diglycol, Thiotrithiazyl perchlorate, Trichloromelamine, 2,4,6-Trichloro-1,3,5-triazine
    [Show full text]
  • United States Patent Office Patented Aug
    3,459,514 United States Patent Office Patented Aug. 5, 1969 2 quired is smaller than the requirements of the prior art. 3,459,514 It is still a further object of the present invention to pro METHOD FOR PREPARING ALKAL vide a process whereby the amount of by-product pro METAL BOROHYDRDES James D. Johnston and Albert P. Giraitis, Baton Rouge, duced is less than that produced by the prior art. Other La., assignors to Ethyl Corporation, New York, N.Y., a objects will become apparent from the ensuing descrip corporation of Virginia tion. No Drawing. Continuation-in-part of applications Ser. No. The above objects are accomplished by the provision 308,691, Sept. 13, 1963, and Ser. No. 322,054, Nov. 7, of a process for producing an alkali metal borohydride 1963. This application Oct. 1, 1964, Ser. No. 400,888 which comprises reacting together an alkali metal hy ret, C. C01b 6/14 O dride, desiccated borax, hydrogen, and silicon at a tem U.S. C. 23-362 6 Claims perature within the range of from about 200 C. to about 900° C. The alkali metal present during the course of the re ABSTRACT OF THE DISCLOSURE action is a member selected from Group I-A of the A method of preparing alkali metal borohydrides com Periodic Chart of the Elements, Fisher Scientific Com prising reacting an alkali metal or alkali metal hydride, pany, 1955. The alkali metals include lithium, sodium, desiccated borax, hydrogen, and silicon, in an inert hy potassium, rubidium, and cesium. Sodium is a preferred drocarbon at about 250° C.
    [Show full text]
  • Sop Pyrophoric 2 12/16/2019
    Owner DOC. NO. REV. DATE C.H.O SOP PYROPHORIC 2 12/16/2019 DOC. TITLE SOP FOR PYROPHORIC CHEMICALS Environmental Health & Safety STANDARD OPERATING PROCEDURES (SOP) FOR WORKING WITH PYROPHORIC CHEMICALS AT AMHERST COLLEGE ___________________________________________________________________ General Information Pyrophoric Chemicals are solid, liquid, or gas compounds that, when exposed to air or moisture at or below 54°C (130°F), can spontaneously ignite. Examples of Pyrophoric chemicals used at Amherst College Laboratories include: sodium hydride, zinc powder, and Grignard reagents. See the “Appendix” page below for a full list of Pyrophoric Chemicals. Pyrophoric chemicals are often used as catalysts in chemical reactions or as reducing and deprotonating agents in organic chemistry. Note that Pyrophoric chemicals may also be characterized by other hazards, hence, users of these chemicals may also need to refer to other SOPs that cover other hazards. In addition, each individual chemical’s Safety Data Sheet (SDS) should be consulted before they are used. _____________________________________________________________________________________ Personal Protective Equipment When working with Pyrophoric Chemicals, the following personal protective equipment (PPE) must be worn, at a minimum. Depending on the specific chemical, other forms of protection might be required. Consult the SDS for each chemical before use: Splash goggles Lab coat (Fire resistant lab coat highly recommended) Long pants Close toed shoes Gloves – Nitrile gloves adequate for accidental contact with small quantities. However, the use of fire resistant Nomex/ Leather Pilot’s gloves is highly recommended _____________________________________________________________________________________ Safety Devices All work with Pyrophoric chemicals must be done in a glove box, vacuum manifold, or any enclosed inert environment. If work must be done in a fume hood, ensure that the hood sash is in the lowest feasible position.
    [Show full text]
  • Innovations Enabled by the U.S. Department of Energy Fuel Cell Technologies Office
    Pathways to Success: Innovations Enabled by the U.S. Department of Energy Fuel Cell Technologies Office November 2018 Prepared by Pacific Northwest National Laboratory for the U.S. Department of Energy Fuel Cell Technologies Office i Notice This report is being disseminated by the U.S. Department of Energy (DOE). As such, this document was prepared in compliance with Section 515 of the Treasury and General Government Appropriations Act for Fiscal Year 2001(Public Law 106-554) and information quality guidelines issued by DOE. Though this report does not constitute “influential” information, as that term is defined in DOE’s information quality guidelines or the Office of Management and Budget’s Information Quality Bulletin for Peer Review, the report was reviewed both internally and externally prior to publication. Reviewers included technical experts from Pacific Northwest National Laboratory and DOE’s Fuel Cell Technologies Office. The views and opinions of the authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof. Neither the United States Government nor any agency thereof, nor any of their employees, makes any warranty, expressed 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. ii Table of Contents Table of Contents ......................................................................................................
    [Show full text]
  • Back Matter (PDF)
    INDEX TO VOLUME 171 (A) Adiabatic piezo-optic coefficient of liquids (Raman and Venkataraman), 137. Allen, J. F. and Ganz, E. The influence of pressure on the thermal conductivity of liquid He n, 242. Appleton, E. V. and Weekes, K. On lunar tides in the upper atmosphere, 171. Arnot, F. L. and Hart, W. D. Electron transfer in argon, 383. Arnot, F. L. and M’Ewen, M. B. The formation of helium molecules, II, 106. Braddick, H. J. J. Cosmic ray bursts at high altitude, 314. Bruce, H. D. Optical thickness of the transition layer between transparent media, 411. Brookman, E. F. See Norrish and Brookman. Budden, K. G., Ratcliffe, J. A. and Wilkes, M. V. Further investigations of very long waves reflected from the ionosphere, 188. Burgoyne, J. H. The combustion of aromatic and alicyclic hydrocarbons, II, 421. Carmichael, H. and Dymond, E. G. High altitude cosmic radiation measure­ ments near the north geomagnetic pole, 321. ------------- Upper air investigations in North-West Greenland, 346. Combustion of aromatic and alicyclic hydrocarbons (Burgoyne), 421. Conn, G. K. T. and Twigg, G. H. Infra-red analysis applied to the exchange reaction between ethylene and deuteroethylene, 70. Copper-cuprous oxide photocells (Mott), 281. Coriolis perturbations in methane spectrum (Jahn), 450. Cosmic radiation near the north pole (Carmichael and Dymond), 321. Cosmic ray bursts at high altitude (Braddick), 314. Coulomb law, deviation for the proton (Frdhlich, Heitler and Kahn), 269. Crystal rectifiers, theory (Mott), 27. Davoud, J. G. and Hinshelwood, C. N. The thermal decomposition of diethyl ether, 39. Diamagnetic anisotropy of organic molecules (Lonsdale), 541.
    [Show full text]
  • Molecular Hydrogen and Catalytic Combustion in the Production Of
    Molecular Hydrogen and Catalytic Combustion in the Production of Hyperpolarized 83Kr and 129Xe MRI Contrast Agents. Nicola J. Rogers1,a, Fraser Hill-Casey1,2, Karl F. Stupic1, b, Joseph S. Six1,c, Clementine Lesbats1, Sean P. Rigby2, Jacques Fraissard3, Galina E. Pavlovskaya1, and Thomas Meersmann1*. 1Sir Peter Mansfield Imaging Centre, University of Nottingham, Nottingham, NG7 2RD, United Kingdom 2Department of Chemical and Environmental Engineering, University of Nottingham, Nottingham NG7 2RD, United Kingdom 3Université Pierre et Marie Curie, Ecole Supérieure de Physique et Chimie Industrielles, 75005 Paris, France aCurrent address; Department of Chemistry, Durham University, South Road, Durham, DH1 3LE, United Kingdom bCurrent address: Division of Magnetics, National Institute of Standards and Technology, Boulder, Colorado, USA, 80305. cCurrent address: Carestream Health Inc., 8124 Pacific Avenue, White City, Oregon, 97503, USA *Author to whom correspondence should be addressed. Electronic mail: [email protected] Keywords: spin exchange optical pumping, hyperpolarized noble gas contrast agents, cryogenic separation, chemical looping combustion, catalytic hydrogen oxidation Classification: Physical Sciences; Applied Physical Sciences. Argon40_vsN29b 2016_01_11 1 Abstract. Hyperpolarized (hp) 83Kr is a promising MRI contrast agent for the diagnosis of pulmonary diseases affecting the surface of the respiratory zone. However, the distinct physical properties of 83Kr that enable unique MRI contrast also complicate the production of hp 83Kr. This work presents a radically new approach in the generation of hp 83Kr that can likewise be utilized for the production of hp 129Xe. Molecular nitrogen, typically used as buffer gas in spin exchange optical pumping (SEOP), was replaced by molecular hydrogen without penalty for the achievable hyperpolarization.
    [Show full text]
  • 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
    [Show full text]
  • Catalytic Tuning of Sorption Kinetics of Lightweight Hydrides: a Review of the Materials and Mechanism
    catalysts Review Catalytic Tuning of Sorption Kinetics of Lightweight Hydrides: A Review of the Materials and Mechanism Ankur Jain 1,*, Shivani Agarwal 2 and Takayuki Ichikawa 3,* 1 Natural Science Centre for Basic Research & Development, Hiroshima University, Higashihiroshima 739-8530, Japan 2 Department of Physics, JECRC University, Jaipur 303905, India; [email protected] 3 Graduate School of Engineering, Hiroshima University, Higashihiroshima 739-8527, Japan * Correspondence: [email protected] or [email protected] (A.J.); [email protected] (T.I.); Tel.: +81-82-424-4609 (A.J.); +81-82-424-5744 (T.I.) Received: 31 October 2018; Accepted: 5 December 2018; Published: 11 December 2018 Abstract: Hydrogen storage materials have been a subject of intensive research during the last 4 decades. Several developments have been achieved in regard of finding suitable materials as per the US-DOE targets. While the lightweight metal hydrides and complex hydrides meet the targeted hydrogen capacity, these possess difficulties of hard thermodynamics and sluggish kinetics of hydrogen sorption. A number of methods have been explored to tune the thermodynamic and kinetic properties of these materials. The thermodynamic constraints could be resolved using an intermediate step of alloying or by making reactive composites with other hydrogen storage materials, whereas the sluggish kinetics could be improved using several approaches such as downsizing and the use of catalysts. The catalyst addition reduces the activation barrier and enhances the sorption rate of hydrogen absorption/desorption. In this review, the catalytic modifications of lightweight hydrogen storage materials are reported and the mechanism towards the improvement is discussed.
    [Show full text]
  • Nomenclature of Inorganic Compounds
    WORKSHEET GENERATORS www.vaxasoftware.com/pc Exercises of Nomenclature of inorganic compounds 1) Give the formula for each of the following: a) beryllium monoxide, beryllium oxide b) water c) dialuminium trioxide, aluminium oxide d) manganese monoxide, manganese(II) oxide e) disodium dioxide, sodium peroxide f) carbon monoxide, carbon(II) oxide 2) Name each of the following compounds: a) Ag2O2 b) CoO c) CdO d) BaO2 e) H2O f) CaO 3) Give the formula for each of the following: a) calcium hydride b) zinc hydride c) aluminium hydride d) phosphine e) francium hydride f) sodium hydride 4) Name each of the following compounds: a) AgH b) CsH c) AsH3 d) BaH2 e) RbH f) KH 5) Give the formula for each of the following: a) nickel(II) hydroxide b) magnesium hydroxide c) copper(I) hydroxide d) caesium hydroxide e) rubidium hydroxide f) calcium hydroxide 6) Name each of the following compounds: a) NaOH b) NH4OH c) Cr(OH)3 d) Fe(OH)2 e) Cr(OH)2 f) Cu(OH)2 1 WORKSHEET GENERATORS www.vaxasoftware.com/pc Exercises of Nomenclature of inorganic compounds 7) Give the formula for each of the following: a) rubidium bromide b) copper(I) chloride c) hydrogen iodide d) beryllium bromide e) dinitrogen triselenide, nitrogen(III) selenide, nitrous selenide f) hydrogen chloride, hydrochloric acid 8) Name each of the following compounds: a) HF b) H2Se(ac) c) NH4Cl d) LiCl e) As2S3 f) HI(ac) 9) Give the formula for each of the following: a) hydrogen chromate, chromic acid b) hydrogen orthophosphate, orthophosphoric acid c) hydrogen seleniate, selenic acid d) hydrogen
    [Show full text]
  • US5354918.Pdf
    |||||||||||||||||US005354918A United States Patent 19 11) Patent Number: 5,354,918 Ohsaki et al. 45) Date of Patent: Oct. 11, 1994 (54 HIGHLY PURE MONOALKYLPHOSPHINE OTHER PUBLICATIONS (75) Inventors: Hiromi Ohsaki; Kazuyuki Asakura, Hoff et al., Journal of Organic Chemistry, (24) pp. both of Joetsu: Masashi Sugiya, 356-359, 1959. Tokyo; Yutaka Demura; Tomio Chemical Abstracts, vol. 117, 1992, Columbus, Ohio, Yanai, both of Kohriyama, all of US; abstract No. 171693s, & JP-A-04 149 187 (Nippon Japan Mining Co., Ltd.). Primary Examiner-Johann Richter 73) Assignees: Shin-Etsu Chemical Co., Ltd.; Nippon Assistant Examiner-Margaret J. Page Chemical Industrial Co., Ltd., both of Japan Attorney, Agent, or Firm-Parkhurst, Wendel & Rossi 57 ABSTRACT (21) Appl. No.: 91,363 The method for preparing a monoalkylphosphine of high purity comprises reacting phosphine and an alkene (22 Filed: Jul. 15, 1993 in the presence of an anhydrous alkanesulfonic acid as a catalyst in a solvent having a boiling point higher than that of the monoalkylphosphine produced. The result 30 Foreign Application Priority Data ing monoalkylphosphine is brought into contact with an Jul. 17, 1992 JP Japan .................................. 4-1904.87 alkali solution to remove the catalyst, which is a sulfur Nov. 9, 1992 JP Japan .... ... 4-298629 atom-containing compound, remaining in the solution. Mar. 12, 1993 JP Japan .................................... 5-51806 The reaction solution from which the remaining cata Mar. 22, 1993 JP Japan .................................... 5-61775 lyst is removed is then brought into contact with alkali metal hydrides or alkaline earth metal hydrides to elimi 51) Int. Cl. ................................................ C07F 9/50 nate any moisture remaining in the reaction solution.
    [Show full text]
  • BNL CHEMICAL STORAGE and COMPATIBILITY TABLE Revision Date: 07-24-07 the Only Official Copy of This Document Is On-Line at the SHSD Website
    BNL CHEMICAL STORAGE AND COMPATIBILITY TABLE Revision Date: 07-24-07 The only official copy of this document is on-line at the SHSD website. Before using a printed copy, verify that it is current by checking the document issue date on the website. http://www.bnl.gov/esh/shsd/Programs/Program_Area_Chemicals_Compatibility.asp Information contained in this table was compiled from the following sources: Academic Laboratory Chemical Hazards Guidebook by William J. Mahn, Published by Van Nostrand, Reinhold, 1991; Fire Protection Guide to Hazardous Materials 11th edition, National Fire Protection Association, 1994; Hazardtext® Hazard Managements Database; INFOTEXT® Documents Database; Better Science Through Safety by Jack A. Gerlovich and Gary E. Downs, © 1981 by the Iowa State University Press. Document Revision Date 07-24-07 Ken Erickson CHO Chemical Chemical Hazard and Compatibility Information Acetic Acid HAZARDS & STORAGE: Corrosive and combustible liquid. Serious health hazard. Reacts with oxidizing and alkali materials. Keep above freezing point (62 ºF) to avoid rupture of carboys and glass containers. INCOMPATIBILITIES: 2-amino-ethanol, Acetaldehyde, Acetic anhydride, Acids, Alcohol, Amines, 2-Amino- ethanol, Ammonia, Ammonium nitrate, 5-Azidotetrazole, Bases, Bromine pentafluoride, Caustics (strong), Chlorosulfonic acid, Chromic Acid, Chromium trioxide, Chlorine trifluoride, Ethylene imine, Ethylene glycol, Ethylene diamine, Hydrogen cyanide, Hydrogen peroxide, Hydrogen sulfide, Hydroxyl compounds, Ketones, Nitric Acid, Oleum, Oxidizers
    [Show full text]
  • United States Patent (19) 11 Patent Number: 4,833,046 Roy (45) Date of Patent: May 23, 1989
    United States Patent (19) 11 Patent Number: 4,833,046 Roy (45) Date of Patent: May 23, 1989 (54) METAL-HYDROGEN SECONDARY 3,960,596 6/1976 Mitoff et al. ........................ 429/185 BATTERY 3,993,502 11/1976 Bjorkman, Jr. ....................... 429/51 4,049,877 9/1977 Saillant et al. ........................ 429/1 75 Inventor: Prodyot Roy, Saratoga, Calif. 4,065,604 12/1977 Zellhoefer ....... ... 429/103 4,123,597 10/1978 Zauner et al. ... ... 429/12 73 Assignee: General Electric Company, San Jose, 4,156,758 5/1979 Vissers et al. ... 429/12 Calif. 4,178,418 12/1979 Croset et al. .... ... 429/27 (21) Appl. No.: 125,624 4,692,390 9/1987 Roy ....................................... 429/17 22 Filed: Nov. 25, 1987 OTHER PUBLICATIONS Linden, D., "Handbook of Batteries & Fuel Cells," pp. Related U.S. Application Data 31-10, 31-12, 32-26, 1984. 63 Continuation of Ser. No. 909,374, Sep. 19, 1986, aban Brogstedt, H., "Material Behavior & Physical Chemis doned. try in Liquid Metal Systems' pp. 297-307, 1982. 511 Int. Cl." ............................................ H01M 10/39 Primary Examiner-Anthony Skapars 52) U.S. Cl. ........................................ 429/50: 429/20; Attorney, Agent, or Firm-Raymond E. Smiley 429/103; 429/112; 429/199; 429/16 58 Field of Search ................................ 429/101-103, (57) ABSTRACT 429/112, 16, 17, 20, 50, 51, 52, 199, 200, 120 A secondary electrochemical cell includes a source of hydrogen as the hydrogen-providing reactant and an 56 References Cited alkali or alkaline earth metal as the metal reactant. Hy U.S. PATENT DOCUMENTS drogen may be from H2 gas or a metal hydride.
    [Show full text]