DOCSLIB.ORG

Standard X-Ray Diffraction Powder Patterns: Section 10

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Standard X-Ray Diffraction Powder Patterns: Section 10 standard X-ray Diffraction Powder Patterns ^v^iSection 10-Data for 84 Substances ^•2. — Howard E. Swanson, Howard F. McMurdie, Marlene C. Morris lliloise H. Evans, and Boris Paretzkin Assisted by Johan H. deGroot and Simon J. Carmel Institute for Materials Research -y.J National Bureau of Standards ' Washington, D.C. 20234 U.S. DEPARTMENT OF COMMERCE, Refer G. Peterson, Secretary NATIONAL BUREAU OF STANDARDS, Lawrence M. Kushner, AcUng Director, Issued November 1972 Library of Congress Catalog Card Number: 53—61386 National Bureau of Standards Monograph 25 Section 10—Data for 84 Substances Nat. Bur. Stand. (U.S.), Monogr. 25— Sec. 10,161 pages (Nov. 1972) CODEN: NBSMA6 For sale by the Superintendent of Documents, U.S. Government Printing Office, Washington, D.C. 20402 (Order by SD Catalog No. C13.44: 25/Sec. 10). Price $2.00 CONTENTS Page Page Introduction 1 Zinc manganese oxide (hetaerolite), ZnMn20^ 61 Experimental patterns: Zinc tin oxide, Zn2Sn04 62 Ammonium aluminum sulfate, NH^AKSO^)^ 5 Calculated patterns: Ammonium copper bromide hydrate, (NH^)2CuBr^"2H20 .. 6 Barium bromide, BaBr2 63 Ammonium iodate, NH^IOj 7 Barium iodide, Bal2 66 Ammonium iron sulfate, NH^Fe(S0^)2 8 Boron oxide, B2O3 phase 1 70 Ammonium magnesium aluminum fluoride, NH^IVIgAIFg ... 9 Calcium iron silicate hydroxide, julgoldite, Barium bromide fluoride, BaBrF 10 Ca2Fe3Si30jo(OH,0)2(OH)2 72 Barium chloride fluoride, BaCIF 11 Calcium malate hydrate, CaC4H405-2H20 76 Barium sulfate (barite), BaSO^ (revised). 12 Cesium lithium cobalt cyanide, CsLiCo(CN)g 79 Cadmium ammine chloride, Cd(NH3)2Cl2 14 Chromium fluoride, CrFj 81 Cadmium fluoride, CdF^ 15 Cobalt ammine iodide, Co(NH3)gl3 83 Cadmium manganese oxide, CdMn^G^ 16 Cobalt fluoride, C0F2 85 Calcium chloride fluoride, CaClF 17 Copper ammine selenate, Cu(NH3)^Se04 87 Calcium platinum oxide, Ca^PtOg 18 Copper ammine sulfate hydrate, Cu(NH3)4SO^'H20 90 Cesium cadmium bromide, CsCdBrj (h-exagonal) 20 Copper uranium oxide, CuUO^ 93 Cesium manganese fluoride, CslVlnFj 21 Iron sulfate hydroxide, butlerite, FeS04(OH)-2H20 95 Holmium fluoride, HoF^ 23 Lithium aluminum, LigAI^ 98 Iron oxalate hydrate (humboldtine) FeC204*2H20 24 Lithiun selenide, Li2Se 100 Lead bromide fluoride, PbBrF 25 Lithium sulfide, Li2S 101 Lead fluoride iodide, PbFI 26 Lithium telluride, Li2Te 102 Lead oxide sulfate, PbjO^SO^ 27 Magnesium iron carbonate hydroxide hydrate, Lead tin oxide, Pb2Sn04 29 sjogrenite, MggFe2C03(OH),g-4H20, phase I 103 Lithium gallium oxide, LiGa02 31 Magnesium iron carbonate hydroxide hydrate, Lithium iodate, LilOj (tetragonal) 33 pyroaurite, MggFe2C03(OH)ig-4H20, phase II 104 Lithium oxalate, 112^20^ 34 Manganese fluoride, MnF2 105 Magnesium manganese oxide, IVlglV!n204 35 Mercury bromate, Hg(Br03)2 107 Magnesium nickel oxide, MgNi02 36 Mercury bromide, HgBr2 110 Magnesium tin oxide, Mg2Sn04 37 Mercury phthalate, CgH4(COOHg)2 113 Manganese oxide (hausmannite), MUjG^ 38 Molybdenum arsenide, MO2AS3 115 Manganese oxide (pyrolusite), beta, Mn02 39 Nickel bromide, NiBr2 119 Mercury amide chloride, HgNH2CI 40 Nickel fluoride, NiF2 121 Potassium magnesium fluoride, K2MgF4 42 Nickel yttrium, Ni3Y 123 Potassium magnesium selenate hydrate, Potassium oxide, K2O 125 K2Mg(Se04)2-6H20 43 Potassium seleniae, K2Se 126 Potassium nickel fluoride, K2NiF4 45 Potassium sulfide, K2S : 127 Potassium zinc fluoride, K2ZnF4 46 Potassium telluride, K2Te 128 Rubidium copper chloride hydrate, Rb2CuCl4*2H20 47 Sodium hydrogen phosphate, Na3H(P03)^ 130 Sodium calcium silicate, Na2CaSi04 48 Sodium oxide, Na20 134 Sodium lanthanum molybdenum oxide, NaLa(Mo04)2 48 Sodium selenide, Na2Se 135 Strontium aluminum hydroxide, Sr2Al2(OH)j2 50 Sodium silicate, beta, Na2Si205 136 Strontium aluminum oxide, Sr3Al20g 52 Sodium sulfide, Na2S 140 Strontium bromide fluoride, SrBrF 54 Sodium telluride, Na2Te 141 Strontium chloride fluoride, SrCIF 55 Strontium manganese oxide, SrMnO^ 56 (hexagonal)l Cumulative index to Circular 539, Volumes 1 through 10, Strontium manganese oxide, SrMnOj (cubic) 58 and Monograph 25, Sections 1 through 10 143 Zinc ammine chloride, Zn(NH3)2Cl2'- 59 Zinc cobalt oxide, ZnCo204 60 Cumulative mineral index 155 1x1 Errata Monograph 25 Section 5, pg. 12. The journal reference for Glasser and Dent Glasser (1963) should be J. Am, Coram. Soc. 46, 377. Section 8, pgs. iii, 135, 164, 166. On each page.change the subscript for silicon in the formula for meliphanite (sodium calcium beryllium aluminum fluoro- silicate). The silicon subscript should be 1.87. Section 9, pg. 36. In the 1st column of the table, line 15, 1.4287 should read 1.4096. Section 9, pg. 6. In the 3rd column of the table, line 9, the entry 320 should read 230. Section 9, pg. 1, column 2; 11th row of text from botton, Avogadro's number should read (6.02252x10") STANDARD X-RAY DIFFRACTION POWDER PATTERNS NBS Monograph 25, Sections 4 thru 10 are available from the Superintendent of Docu- ments, U.S. Government Printing Office, Washington, D.C., 20402 as follows; NBS Monograph 25, Section 4, 55 cents; Section 5, 55 cents; Section 6, 60 cents; Section 7, $1.50; Section 8, $1.50; Section 9, $1.25. Remittance from foreign countries should include an additional one-fourth of the purchase price for postage. (Order by SD Catalog No. C 13.44:25/Sec.-) Those wishing to be notified of future issues should send mailing address to the Government Printing Office. NBS Monograph 25, Section 2 and 3, and Circular 539 Volumes 1,2,5,8, and 10 may be obtained from Mr. Howard E. Swanson, Room A221, Materials Building, National Bureau of Standards, Washington, D.C. 20234. The following "out of print" copies may be obtained from the National Technical Information Service, 5285 Port Royal Road, Springfield, Virginia, 22151. These publica- tions will be identified with a "PB" number which must be used in ordering. The publications are $6.00 each hardcopy and 95 cents each microfische. Foreign countries should include an additional $2.50 for each hardcopy and $1.50 for each microfische for postage. NBS Publication Number PB Number Circular 539, Vol. 3 178 904 Circular 539, Vol. 4 178 905 Circular 539, Vol. 6 178 907 Circular 539, Vol. 7 178 908 Circular 539, Vol. 9 178 910 Mono. 25, Sect. 1 178 429 . STANDARD X-RAY DIFFRACTION POWDER PATTERNS Section 10 - Data for 84 substances Howard E. Swanson, Howard F. McMurdie,' Marlene C. Morris/ Eioise H. Evans,^ and Boris Paretzkin^ Assisted by Johan H. deGroot^ and Simon J. Carmel Standaid x-ray diffraction patterns are presented for 84 substances. Forty-seven of ttiese patterns represent experimental data and 37 are calculated. The experimental x-ray powder diffraction patterns were obtained with an x-ray diffradometer. All d-values were assigned Miller indices determined by comparison with computed inlerplanar spacings consistent with space group extinctions. The densities and lattice constants were calculated, and the refractive indices were measured whenever possible. The calculated x-ray powder diffraction patterns were computed from published crystal structure data. Both peak height and integrated intensities are re- ported for the calculated patterns. Key words: Crystal structure; integrated intensities; lattice constants; peak intensities; powder patterns; reference intensities; standard; x-ray diffraction. INTRODUCTION Optical data, color. A microscopic inspection for phase purity was also made on the non-opaque materials during The Powder Diffraction File is a continuing compilation of the refractive index determination. The latter was done by diffraction patterns gathered from many sources. Produced and gram-immersion methods in white light, using oils standardized published by the Joint Committee on Powder Diffraction Stand- in sodium light, in the refractive index range 1.40 to 2.1 ards,^ the File is used for identification of crystalline [Hartshorne and Stuart, 1960] materials by matching d-spacings and diffraction intensity The names of the sample colors were selected from the measurements. Under the partial sponsorship of the Joint ISCC-NBS Centroid Color Charts [1965]. Committee, the program at the National Bureau of Standards contributes new data to this File. Our work also aids in the Structure, lattice coristants. The space groups evaluation and revision of published x-ray data and in the were listed with short Hermann-Mauguin symbols as well as development of diffraction techniques. This report presents the space group numbers given in the International Tables for information for 84 compounds (47 experimental and 37 calcu- X-ray Crystallography Vol. I [1952]. lated patterns), and is the twentieth of the series of "Standard Orthorhombic cell dimensions were arranged according to X-ray Diffraction Powder Patterns.'"' the Dana convention b>a>c [Palache et al., 1944] . A computer program [Evans et al., 1963] assigned hki's and refined the lattice constants. Cell refinement was based EXPERIMENTAL POWDER PATTERNS only upon 29 values which could be indexed without ambiguity. In indexing cubic patterns, multiple hk£'s were not reported; Sample. The samples used to make NBS patterns were instead, we chose the single appropriate index having the obtained from a variety of sources or were prepared in small largest h. The number of significant figures reported for d- quantities in our laboratory. Appropriate annealing, recrys- values varied with the symmetry and crystallinity of each tallizing, or heating in hydrothermal bombs improved thequality sample. Unit cell constants and their standard errors were of most of the patterns. A check of phase purity was provided based on least-squares refinement of the variance-covariance by indexing the x-ray pattern. matrix derived from the unweighted A9 residuals. These stand- ard errors derived by the computer program should be increased in most cases. An increase should also be applied to all '^Consultant and Research Associates, respectively, of the Joint Committee on lattice constant errors in earlier publications of this series. Powder Diffraction Standards Associateship at the National Bureau of Standards. Densities. These were calculated from the NBS lattice 'joint Committee on Powder Diffraction Standards, 1601 Park Lane, Swarthmore, constants, the Avogadro number (6.02252 x lO^-'), and atomic Pa.
Load more

Recommended publications
  • WO 2015/025175 Al 26 February 2015 (26.02.2015) P O P C T
    (12) INTERNATIONAL APPLICATION PUBLISHED UNDER THE PATENT COOPERATION TREATY (PCT) (19) World Intellectual Property Organization International Bureau (10) International Publication Number (43) International Publication Date WO 2015/025175 Al 26 February 2015 (26.02.2015) P O P C T (51) International Patent Classification: (81) Designated States (unless otherwise indicated, for every C09K 5/06 (2006.01) kind of national protection available): AE, AG, AL, AM, AO, AT, AU, AZ, BA, BB, BG, BH, BN, BR, BW, BY, (21) International Application Number: BZ, CA, CH, CL, CN, CO, CR, CU, CZ, DE, DK, DM, PCT/GB2014/052580 DO, DZ, EC, EE, EG, ES, FI, GB, GD, GE, GH, GM, GT, (22) International Filing Date: HN, HR, HU, ID, IL, IN, IR, IS, JP, KE, KG, KN, KP, KR, 22 August 2014 (22.08.2014) KZ, LA, LC, LK, LR, LS, LT, LU, LY, MA, MD, ME, MG, MK, MN, MW, MX, MY, MZ, NA, NG, NI, NO, NZ, (25) Filing Language: English OM, PA, PE, PG, PH, PL, PT, QA, RO, RS, RU, RW, SA, (26) Publication Language: English SC, SD, SE, SG, SK, SL, SM, ST, SV, SY, TH, TJ, TM, TN, TR, TT, TZ, UA, UG, US, UZ, VC, VN, ZA, ZM, (30) Priority Data: ZW. 13 15098.2 23 August 2013 (23.08.2013) GB (84) Designated States (unless otherwise indicated, for every (71) Applicant: SUNAMP LIMITED [GB/GB]; Unit 1, Satel kind of regional protection available): ARIPO (BW, GH, lite Place, Macmerry, Edinburgh EH33 1RY (GB). GM, KE, LR, LS, MW, MZ, NA, RW, SD, SL, ST, SZ, TZ, UG, ZM, ZW), Eurasian (AM, AZ, BY, KG, KZ, RU, (72) Inventors: BISSELL, Andrew John; C/o SunAmp, Unit TJ, TM), European (AL, AT, BE, BG, CH, CY, CZ, DE, 1, Satellite Place, Macmerry, Edinburgh EH33 1RY (GB).
    [Show full text]
  • Download Author Version (PDF)
    Journal of Materials Chemistry A Accepted Manuscript This is an Accepted Manuscript, which has been through the Royal Society of Chemistry peer review process and has been accepted for publication. Accepted Manuscripts are published online shortly after acceptance, before technical editing, formatting and proof reading. Using this free service, authors can make their results available to the community, in citable form, before we publish the edited article. We will replace this Accepted Manuscript with the edited and formatted Advance Article as soon as it is available. You can find more information about Accepted Manuscripts in the Information for Authors. Please note that technical editing may introduce minor changes to the text and/or graphics, which may alter content. The journal’s standard Terms & Conditions and the Ethical guidelines still apply. In no event shall the Royal Society of Chemistry be held responsible for any errors or omissions in this Accepted Manuscript or any consequences arising from the use of any information it contains. www.rsc.org/materialsA Page 1 of 9 Journal of Materials Chemistry A ARTICLE JMCA Safer Salts for CdTe Nanocrystal Solution Processed Solar Cells: The Dual Roles of Ligand Exchange and Grain Growth Received 00th January 20xx, a b c d e Accepted 00th January 20xx Troy K. Townsend, † William B. Heuer, Edward E. Foos, Eric Kowalski, Woojun Yoon and Joseph G. Tischler e DOI: 10.1039/x0xx00000x Inorganic CdSe/CdTe nanocrystals for solid-state photovoltaic devices are typically sintered into a bulk-like material after www.rsc.org/ annealing in the presence of solid cadmium chloride.
    [Show full text]
  • Severe Corrosion of Steel and Copper by Strontium Bromide In
    Corrosion Science 138 (2018) 275–283 Contents lists available at ScienceDirect Corrosion Science journal homepage: www.elsevier.com/locate/corsci Severe corrosion of steel and copper by strontium bromide in T thermochemical heat storage reactors ⁎ Pierre D’Ansa, , Emilie Courbonb, Marc Frèreb, Gilbert Descyc, Tiriana Segatoa, Marc Degreza a Université Libre de Bruxelles (ULB), 4MAT Department, 50, Avenue F.D. Roosevelt, CP194/03, 1050, Brussels, Belgium b UMONS, Institut de Recherche en Energie – Laboratoire de Thermodynamique, 31 Boulevard Dolez, 7000, Mons, Belgium c BE-SOL R&D, 2 rue de la Griotte, 5580, Rochefort, Belgium ARTICLE INFO ABSTRACT Keywords: Thermochemical heat storage exploits thermal solar energy to produce sustainable residential heating, obtained A. Copper by exothermal reaction between bromides and water vapour. A protocol to test the corrosion of surrounding A. Carbon steel −1 materials is discussed in the case of SrBr2 contacting copper or steel. Corrosion depth > 1 mm y is found for B. Weight loss steel in conditions where the salt remains mostly solid, due to a reaction between SrBr2 and atmospheric CO2 B. XRD that produces HBr. Temperature and the dissolution of the salt (deliquescence) also play a key role. B. Cyclic voltammetry Potentiodynamic tests, the limitations of which are discussed, corroborate the salt degradation in the case of C. Reactor conditions steel. 1. Introduction Since the late eighties, several papers have been dedicated to the corrosion problem in the case of PCMs, with tests focused on the While electrical power storage is becoming widespread through melting process or the liquid phase [21–34], and quite often in organic applications like electrical vehicles, thermal energy storage still needs compounds [30,35,36].
    [Show full text]
  • PDF Card 3-320 [Dow Chemical Co., Midland, 1 .3805 1 006 67.83 Michigan] 1 .3672 6 300 68.58
    standard X-ray Diffraction Powder Patterns ^v^iSection 10-Data for 84 Substances ^•2. — Howard E. Swanson, Howard F. McMurdie, Marlene C. Morris lliloise H. Evans, and Boris Paretzkin Assisted by Johan H. deGroot and Simon J. Carmel Institute for Materials Research -y.J National Bureau of Standards ' Washington, D.C. 20234 U.S. DEPARTMENT OF COMMERCE, Refer G. Peterson, Secretary NATIONAL BUREAU OF STANDARDS, Lawrence M. Kushner, AcUng Director, Issued November 1972 Library of Congress Catalog Card Number: 53—61386 National Bureau of Standards Monograph 25 Section 10—Data for 84 Substances Nat. Bur. Stand. (U.S.), Monogr. 25— Sec. 10,161 pages (Nov. 1972) CODEN: NBSMA6 For sale by the Superintendent of Documents, U.S. Government Printing Office, Washington, D.C. 20402 (Order by SD Catalog No. C13.44: 25/Sec. 10). Price $2.00 CONTENTS Page Page Introduction 1 Zinc manganese oxide (hetaerolite), ZnMn20^ 61 Experimental patterns: Zinc tin oxide, Zn2Sn04 62 Ammonium aluminum sulfate, NH^AKSO^)^ 5 Calculated patterns: Ammonium copper bromide hydrate, (NH^)2CuBr^"2H20 .. 6 Barium bromide, BaBr2 63 Ammonium iodate, NH^IOj 7 Barium iodide, Bal2 66 Ammonium iron sulfate, NH^Fe(S0^)2 8 Boron oxide, B2O3 phase 1 70 Ammonium magnesium aluminum fluoride, NH^IVIgAIFg ... 9 Calcium iron silicate hydroxide, julgoldite, Barium bromide fluoride, BaBrF 10 Ca2Fe3Si30jo(OH,0)2(OH)2 72 Barium chloride fluoride, BaCIF 11 Calcium malate hydrate, CaC4H405-2H20 76 Barium sulfate (barite), BaSO^ (revised). 12 Cesium lithium cobalt cyanide, CsLiCo(CN)g 79 Cadmium
    [Show full text]
  • Graphitic Carbon Nitride (G-C3N4), an Organic Semiconductor That Proved a Suitable Photocatalyst for Hydrogen Production from Water
    METAL LOADED G-C₃N₄ FOR VISIBLE LIGHT-DRIVEN H₂ PRODUCTION Federica Fina A Thesis Submitted for the Degree of PhD at the University of St Andrews 2014 Full metadata for this item is available in St Andrews Research Repository at: http://research-repository.st-andrews.ac.uk/ Please use this identifier to cite or link to this item: http://hdl.handle.net/10023/6322 This item is protected by original copyright This item is licensed under a Creative Commons Licence Metal loaded g-C3N4 for visible light-driven H2 production by Federica Fina A thesis submitted in partial fulfilment for the degree of PhD at the University of St Andrews 2014 I, Federica Fina hereby certify that this thesis, which is approximately 50,000 words in length, has been written by me, and that it is the record of work carried out by me and that it has not been submitted in any previous application for a higher degree. I was admitted as a research student in January 2011 and as a candidate for the degree of Doctor of Philosophy in August 2014; the higher study for which this is a record was carried out in the University of St Andrews between 2011 and 2014. Date …………….………….. Signature of candidate …………….………….. I hereby certify that the candidate has fulfilled the conditions of the Resolution and Regulations appropriate for the degree of Doctor of Philosophy in the University of St Andrews and that the candidate is qualified to submit this thesis in application for that degree. Date …………….………….. Signature of supervisor …………….………….. In submitting this thesis to the University of St Andrews I understand that I am giving permission for it to be made available for use in accordance with the regulations of the University Library for the time being in force, subject to any copyright vested in the work not being affected thereby.
    [Show full text]
  • Ab-Initio Spectroscopic Characterization of Melem-Based Graphitic Carbon Nitride Polymorphs
    nanomaterials Article Ab-Initio Spectroscopic Characterization of Melem-Based Graphitic Carbon Nitride Polymorphs Aldo Ugolotti and Cristiana Di Valentin * Dipartimento di Scienza dei Materiali, Università degli Studi di Milano-Bicocca, Via Cozzi 55, 20125 Milano, Italy * Correspondence: [email protected] Abstract: Polymeric graphitic carbon nitride (gCN) compounds are promising materials in photoacti- vated electrocatalysis thanks to their peculiar structure of periodically spaced voids exposing reactive pyridinic N atoms. These are excellent sites for the adsorption of isolated transition metal atoms or small clusters that can highly enhance the catalytic properties. However, several polymorphs of gCN can be obtained during synthesis, differing for their structural and electronic properties that ultimately drive their potential as catalysts. The accurate characterization of the obtained material is critical for the correct rationalization of the catalytic results; however, an unambiguous experimental identification of the actual polymer is challenging, especially without any reference spectroscopic features for the assignment. In this work, we optimized several models of melem-based gCN, taking into account different degrees of polymerization and arrangement of the monomers, and we present a thorough computational characterization of their simulated XRD, XPS, and NEXAFS spectroscopic properties, based on state-of-the-art density functional theory calculations. Through this detailed study, we could identify the peculiar fingerprints of each model and correlate them with its structural and/or electronic properties. Theoretical predictions were compared with the experimental data Citation: Ugolotti, A.; Di Valentin, C. whenever they were available. Ab-Initio Spectroscopic Characterization of Melem-Based Keywords: graphitic carbon nitride; melon; melem polymerization; XPS; NEXAFS; XRD; DFT; Graphitic Carbon Nitride surface science Polymorphs.
    [Show full text]
  • 20210311 IAEG AD-DSL V5.0 for Pdf.Xlsx
    IAEGTM AD-DSL Release Version 4.1 12-30-2020 Authority: IAEG Identity: AD-DSL Version number: 4.1 Issue Date: 2020-12-30 Key Yellow shading indicates AD-DSL family group entries, which can be expanded to display a non-exhaustive list of secondary CAS numbers belonging to the family group Substance Identification Change Log IAEG Regulatory Date First Parent Group IAEG ID CAS EC Name Synonyms Revision Date ECHA ID Entry Type Criteria Added IAEG ID IAEG000001 1327-53-3 215-481-4 Diarsenic trioxide Arsenic trioxide R1;R2;D1 2015-03-17 2015-03-17 100.014.075 Substance Direct Entry IAEG000002 1303-28-2 215-116-9 Diarsenic pentaoxide Arsenic pentoxide; Arsenic oxide R1;R2;D1 2015-03-17 2015-03-17 100.013.743 Substance Direct Entry IAEG000003 15606-95-8 427-700-2 Triethyl arsenate R1;R2;D1 2015-03-17 2017-08-14 100.102.611 Substance Direct Entry IAEG000004 7778-39-4 231-901-9 Arsenic acid R1;R2;D1 2015-03-17 2015-03-17 100.029.001 Substance Direct Entry IAEG000005 3687-31-8 222-979-5 Trilead diarsenate R1;R2;D1 2015-03-17 2017-08-14 100.020.890 Substance Direct Entry IAEG000006 7778-44-1 231-904-5 Calcium arsenate R1;R2;D1 2015-03-17 2017-08-14 100.029.003 Substance Direct Entry IAEG000009 12006-15-4 234-484-1 Cadmium arsenide Tricadmium diarsenide R1;R2;D1 2017-08-14 2017-08-14 Substance Direct Entry IAEG000021 7440-41-7 231-150-7 Beryllium (Be) R2 2015-03-17 2019-01-24 Substance Direct Entry IAEG000022 1306-19-0 215-146-2 Cadmium oxide R1;R2;D1 2015-03-17 2017-08-14 100.013.770 Substance Direct Entry IAEG000023 10108-64-2 233-296-7 Cadmium
    [Show full text]
  • Material Safety Data Sheet 1. Identification of the Substances
    www.himedialabs.com Material Safety Data Sheet According to Regulation (EC) No. 1907/2006 Revision: 01 Date of Revision: 01.07.2017 1. Identification of the substances/ mixture and of the company/ undertaking 1.1 Product Identifiers Product Code GRM2028 Product Name Cadmium fluoride, Hi-AR™ 1.2 Relevant identified uses of the substance or mixture and uses advised against Identified uses Laboratory chemicals, Manufacture of substances 1.3 Details of the supplier of the safety data sheet Produced by HiMedia Laboratories Pvt. Ltd. Address 23, Vadhani Indl.Estate, LBS Marg, Mumbai 400 086, India. Tel. No. +91-22-2500 0970, +91-22-2500 1607 Fax No. +91-22-2500 2468 1.4 Emergency Tel. No. Emergency Tel.No. Please contact the regional HiMedia representation in your country 2. Hazards Identification 2.1 Classification of the substance or mixture Classification according to Regulation (EC) No 1272/2008 [EU-GHS/CLP] Acute toxicity,oral (Category 3) Acute toxicity,inhalation (Category 1, 2) Germ cell mutagenicity (Category 1A, 1B) Carcinogenicity (Category 1A, 1B) Specific target organ toxicity, repeated exposure (Category 1) Hazardous to the aquatic environment, long-term hazard (Category 1) Classification according to EU Directives 67/548/EEC or 1999/45/EC May cause cancer. May cause heritable genetic damage. May impair fertility. May cause harm to the unborn child. Toxic if swa!lowed. Very toxic by inhalation. Toxic: danger of serious damage to health by prolonged exposure through inhalation and if swallowed. Very toxic to aquatic organisms,may cause long-term adverse. Effects in the aquatic environment. 2.2 Label elements Labelling according Regulation (EC) No 1272/2008 [CLP] Pictogram Signal word Danger Hazard Statement(s) H301 Toxic if swallowed H330 Fatal if inhaled H340 May cause genetic defects H350 May cause cancer H372 Causes damage to organs through prolonged or repeated exposure H410 Very toxic to aquatic life with long lasting effects Precautionary Statement(s) P201 Obtain special instructions before use.
    [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]
  • Chemistry of Strontium in Natural Water
    Chemistry of Strontium in Natural Water GEOLOGICAL SURVEY WATER-SUPPLY PAPER 1496 This water-supply paper was printed as separate chapters A-D UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1963 UNITED STATES DEPARTMENT OF THE INTERIOR STEWART L. UDALL, Secretary GEOLOGICAL SURVEY Thomas B. Nolan, Director The U.S. Geological Survey Library has cataloged this publication as follows: U.S. Geological Survey. Chemistry of strontium in natural water. Washington, U.S. Govt. Print. Off., 1962. iii, 97 p. illus., diagrs., tables. 24 cm. (Its Water-supply paper 1496) Issued as separate chapters A-D. Includes bibliographies. 1. Strontium. 2. Water-Analysis. I. Title. (Series) CONTENTS [The letters in parentheses preceding the titles are those used to designate the separate chapters] Page (A) A survey of analytical methods for the determination of strontium in natural water, by C. Albert Horr____________________________ 1 (B) Copper-spark method for spectrochemical determination of strontirm in water, by Marvin W. Skougstad-______-_-_-_--_~__-___-_- 19 (C) Flame photometric determination of strontium in natural water, by C. Albert Horr_____._____._______________... 33 (D) Occurrence and distribution of strontium in natural water, by Margin W. Skougstad and C. Albert Horr____________.___-._-___-. 55 iii A Survey of Analytical Methods fc r The Determination of Strontium in Natural Water By C. ALBERT HORR CHEMISTRY OF STRONTIUM IN NATURAL rVATER GEOLOGICAL SURVEY WATER-SUPPLY PAPER 1496-A This report concerns work done on behalf of the U.S. Atomic Energy Commission and is published with the permission of the Commission UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1959 UNITED STATES DEPARTMENT OF THE INTERIOR FRED A.
    [Show full text]
  • Draft Chemicals (Management and Safety) Rules, 20Xx
    Draft Chemicals (Management and Safety) Rules, 20xx In exercise of the powers conferred by Sections 3, 6 and 25 of the Environment (Protection) Act, 1986 (29 of 1986), and in supersession of the Manufacture, Storage and Import of Hazardous Chemical Rules, 1989 and the Chemical Accidents (Emergency Planning, Preparedness and Response) Rules, 1996, except things done or omitted to be done before such supersession, the Central Government hereby makes the following Rules relating to the management and safety of chemicals, namely: 1. Short Title and Commencement (1) These Rules may be called the Chemicals (Management and Safety) Rules, 20xx. (2) These Rules shall come into force on the date of their publication in the Official Gazette. Chapter I Definitions, Objectives and Scope 2. Definitions (1) In these Rules, unless the context otherwise requires (a) “Act” means the Environment (Protection) Act, 1986 (29 of 1986) as amended from time to time; (b) “Article” means any object whose function is determined by its shape, surface or design to a greater degree than its chemical composition; (c) “Authorised Representative” means a natural or juristic person in India who is authorised by a foreign Manufacturer under Rule 6(2); (d) “Chemical Accident” means an accident involving a sudden or unintended occurrence while handling any Hazardous Chemical, resulting in exposure (continuous, intermittent or repeated) to the Hazardous Chemical causing death or injury to any person or damage to any property, but does not include an accident by reason only
    [Show full text]
  • Triazine-Based Carbon Nitrides for Visible-Light-Driven Hydrogen Evolution
    Triazine-based Carbon Nitrides for Visible-Light-Driven Hydrogen Evolution K. Schwinghammer, B. Tuffy, M. B. Mesch, E. Wirnhier, C. Martineau, F. Taulelle, W. Schnick, J. Senker, and B. V. Lotsch The efficient conversion of solar energy into chemical energy is a major challenge of modern materials chemistry and energy research. One solution to the future’s energy demands will be the generation of hydrogen by photochemical water splitting as an environmentally clean energy carrier with a high energy density. So far the majority of photocatalysts are of an inorganic nature containing heavy metals which increase cost, impede scalability, and add complexity. Therefore, the development of efficient, stable, economically feasible, and environmentally friendly catalysts is required. For many years carbon nitrides (CxNyHz) were famed for their structural variety and potential as precursors for ultra-hard materials. The thermal condensation of simple carbon nitrides (CNs) can form several denser chemical species that differ with respect to their degree of condensation, hydrogen content, crystallinity and morphology. The discovery of extended carbon nitrides with semiconducting properties and band gaps < 3 eV makes them an attractive alternative to metal-rich semiconductors for photocatalysis. In 2009, Wang et al. investigated and determined for the first time the photocatalytic activity of polymeric melon-type CNs based on imide-bridged heptazine units (Fig. 1a).[1] Further publications focused on the modifications of those heptazine based carbon nitrides to improve their photocatalytic activity, e.g. by expanding their surface area, as well as by doping with heteroatoms and organic compounds, which gives rise to an enhanced absorption in the visible light range of the electromagnetic spectrum.
    [Show full text]