Periodic Trends in the Main Group Elements
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Electronic Supplementary Material (ESI) for Chemical Communications This journal is © The Royal Society of Chemistry 2011 Supporting Information for: 2- Quadruple-CO3 Bridged Octanuclear Dysprosium(III) Compound Showing Single-Molecule Magnet Behaviour Experimental Section Synthetic procedures All chemicals were of reagent grade and were used without any further purification. Synthesis of pyrazine-2-carbohydrazide The pyrazine-2-carboxylic acid methyl ester was prepared by a literature procedure described elsewhere. A mixture of pyrazine-2-carboxylic acid methyl ester (1.38 g, 10 mmol) and hydrazine hydrate (85%, 15 ml) in methanol (20 ml) was refluxed overnight, at a temperature somewhat below 80°C. The resulting pale-yellow solution set aside 12 hrs. During this period, a colorless product, i.e. pyrazine-2-carbohydrazide, precipitated from the reaction mixture as a crystalline solid (yield = 0.84 g, 61%). Synthesis of (E)-N'-(2-hyborxy-3-methoxybenzylidene)pyrazine-2-carbohydrazide Pyrazine-2-carbohydrazide (2 mmol, 0.276 g) was suspended together with o-vanillin (2 mmol, 0.304 g) in methanol (20 ml), and the resulting mixture was stirred at the room temperature overnight. The pale yellow solid was collected by filtration (yield = 0.56 g, 83%). Elemental analysis (%) calcd for C13H12N4O3: C, 57.35, H, 4.44, N, 20.58: found C, 57.64, H, 4.59, N, 20.39. IR (KBr, cm-1): 3415(w), 3258(w), 1677(vs), 1610(s), 1579(m). 1530(s), 1464(s), 1363(m), 1255(vs), 1153(s), 1051(w), 1021(s), 986(w), 906(m), 938(w), 736(s), 596(m), 498(w). Synthesis of the complex 1 The solution of DyCl3⋅6H2O (56.5 mg, 0.15 mmol) and the H2L (40.5 mg, 0.15 mmol) in 15 ml CH3OH/CH2Cl2 (1:2 v/v) was stirred with triethylamine (0.4 mmol) for 6h. -
UNITED STATES PATENT Office SVEND S
Patented May 24, 1932 1,859,998 UNITED STATES PATENT oFFICE SVEND S. SVENDSEN, OF CHICAGO, ILLINOIS, ASSIGNOR TO CLAY REDUCTION comi PANY, OF CHICAGO, ILLINOIS, A CORPORATION OF ILLINOIs . HYDRATED SILICA No Drawing. Application filed December 23, 1927. Serial No. 242,291. This invention relates to the production of silicofluoride is also volatilized and collected hydrated silica from a silicious material such in aqueous animonia. The volatilization oc as silica and silicates generally. - - - - curs about 300 C. The following reactions According to the invention the silicious take place in the aqueous ammonia at tem 5 material is treated with ammonium fluoride peratures below 34 C.: 5 5 or bifluoride and silicon ammonia fluorine compounds are produced. These compounds 2SiF(NH) +2H.O= are volatilized and converted into hydrated (NH4)2SiFs--SiO, (hydrated) + silica by the action of water and ammonia. 2NH.F. (IV) O Metallic silicates or substances containing (NH)SiF+4NH,+2HO = them can be subjected to this treatment di SiO, (hydrated) + 6NH.F. (V) rectly. In treating silica in the form of quartz it is found to be necessary to subject It is thus apparent that O heating the it to a preliminary treatment in order to fa silicious material with the ammonium-flu cilitate the action of the ammonium fluoride oride, ammonia-silicon-fluorine compounds a or bifluoride thereon. A suitable preliminary are formed, and by employing suitable tem treatment is to heat the quartz to a bright red peratures are volatilized from the reaction heat and suddenly cool it by immersion in mixture. These compounds may be silicon water. -
Identification of a Chemical Fingerprint Linking the Undeclared 2017 Release of 106Ru to Advanced Nuclear Fuel Reprocessing
Identification of a chemical fingerprint linking the undeclared 2017 release of 106Ru to advanced nuclear fuel reprocessing Michael W. Cookea,1, Adrian Bottia, Dorian Zokb, Georg Steinhauserb, and Kurt R. Ungara aRadiation Protection Bureau, Health Canada, Ottawa, ON K1A 1C1, Canada; and bInstitute of Radioecology and Radiation Protection, Leibniz Universität Hannover, 30419 Hannover, Germany Edited by Kristin Bowman-James, University of Kansas, Lawrence, KS, and accepted by Editorial Board Member Marcetta Y. Darensbourg May 1, 2020 (received for review February 7, 2020) The undeclared release and subsequent detection of ruthenium- constitutes the identification of unique signatures. From a radiologi- 106 (106Ru) across Europe from late September to early October of cal perspective, there is none. Samples have been shown to be radi- 2017 prompted an international effort to ascertain the circum- opure and to carry the stable ruthenium isotopic signature of civilian stances of the event. While dispersion modeling, corroborated spent nuclear fuel (10), while stable elemental analysis by scanning by ground deposition measurements, has narrowed possible loca- electron microscopy and neutron activation has revealed no detect- tions of origin, there has been a lack of direct empirical evidence to able anomalies compared to aerosol filter media sampled prior to the address the nature of the release. This is due to the absence of advent of the 106Ru contaminant (1, 11). We are, then, left with the radiological and chemical signatures in the sample matrices, con- definition of a limiting case for a nuclear forensic investigation. sidering that such signatures encode the history and circumstances Fortunately, we are concerned with an element that has sig- of the radioactive contaminant. -
Hydrous Hydrazine Decomposition for Hydrogen Production Using of Ir/Ceo2: Effect of Reaction Parameters on the Activity
nanomaterials Article Hydrous Hydrazine Decomposition for Hydrogen Production Using of Ir/CeO2: Effect of Reaction Parameters on the Activity Davide Motta 1, Ilaria Barlocco 2 , Silvio Bellomi 2, Alberto Villa 2,* and Nikolaos Dimitratos 3,* 1 Cardiff Catalysis Institute, School of Chemistry, Cardiff University, Cardiff CF10 3AT, UK; [email protected] 2 Dipartimento di Chimica, Università degli Studi di Milano, 20133 Milano, Italy; [email protected] (I.B.); [email protected] (S.B.) 3 Dipartimento di Chimica Industriale e dei Materiali, Alma Mater Studiorum Università di Bologna, 40136 Bologna, Italy * Correspondence: [email protected] (A.V.); [email protected] (N.D.) Abstract: In the present work, an Ir/CeO2 catalyst was prepared by the deposition–precipitation method and tested in the decomposition of hydrazine hydrate to hydrogen, which is very important in the development of hydrogen storage materials for fuel cells. The catalyst was characterised using different techniques, i.e., X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), scanning electron microscopy (SEM) equipped with X-ray detector (EDX) and inductively coupled plasma—mass spectroscopy (ICP-MS). The effect of reaction conditions on the activity and selectivity of the material was evaluated in this study, modifying parameters such as temperature, the mass of the catalyst, stirring speed and concentration of base in order to find the optimal conditions of reaction, which allow performing the test in a kinetically limited regime. Citation: Motta, D.; Barlocco, I.; Bellomi, S.; Villa, A.; Dimitratos, N. Keywords: iridium; cerium oxide; hydrous hydrazine; hydrogen production Hydrous Hydrazine Decomposition for Hydrogen Production Using of Ir/CeO2: Effect of Reaction Parameters on the Activity. -
Elemental Fluorine Product Information (Pdf)
Elemental Fluorine Contents 1 Introduction ............................................................................................................... 4 2.1 Technical Application of Fluorine ............................................................................. 5 2.2 Electronic Application of Fluorine ........................................................................... 7 2.3 Fluorine On-Site Plant ............................................................................................ 8 3 Specifications ............................................................................................................ 9 4 Safety ...................................................................................................................... 10 4.1 Maintenance of the F2 system .............................................................................. 12 4.2 First Aid ................................................................................................................ 13 5.1 Chemical Properties ............................................................................................. 14 5.2 Physical Data ....................................................................................................... 15 6 Toxicity .................................................................................................................... 18 7 Shipping and Transport ........................................................................................... 20 8 Environment ........................................................................................................... -
140. Sulphuric, Hydrochloric, Nitric and Phosphoric Acids
nr 2009;43(7) The Nordic Expert Group for Criteria Documentation of Health Risks from Chemicals 140. Sulphuric, hydrochloric, nitric and phosphoric acids Marianne van der Hagen Jill Järnberg arbete och hälsa | vetenskaplig skriftserie isbn 978-91-85971-14-5 issn 0346-7821 Arbete och Hälsa Arbete och Hälsa (Work and Health) is a scientific report series published by Occupational and Enviromental Medicine at Sahlgrenska Academy, University of Gothenburg. The series publishes scientific original work, review articles, criteria documents and dissertations. All articles are peer-reviewed. Arbete och Hälsa has a broad target group and welcomes articles in different areas. Instructions and templates for manuscript editing are available at http://www.amm.se/aoh Summaries in Swedish and English as well as the complete original texts from 1997 are also available online. Arbete och Hälsa Editorial Board: Editor-in-chief: Kjell Torén Tor Aasen, Bergen Kristina Alexanderson, Stockholm Co-editors: Maria Albin, Ewa Wigaeus Berit Bakke, Oslo Tornqvist, Marianne Törner, Wijnand Lars Barregård, Göteborg Eduard, Lotta Dellve och Roger Persson Jens Peter Bonde, Köpenhamn Managing editor: Cina Holmer Jörgen Eklund, Linköping Mats Eklöf, Göteborg © University of Gothenburg & authors 2009 Mats Hagberg, Göteborg Kari Heldal, Oslo Arbete och Hälsa, University of Gothenburg Kristina Jakobsson, Lund SE 405 30 Gothenburg, Sweden Malin Josephson, Uppsala Bengt Järvholm, Umeå ISBN 978-91-85971-14-5 Anette Kærgaard, Herning ISSN 0346–7821 Ann Kryger, Köpenhamn http://www.amm.se/aoh -
Download Author Version (PDF)
PCCP 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/pccp Page 1 of 24 Physical Chemistry Chemical Physics Disulfuric acid dissociated by two water molecules: Ab initio and density functional theory calculations Seong Kyu Kim, 1,* Han Myoung Lee, 2 Kwang S. Kim 2,* 1 Department of Chemistry, Sungkyunkwan University, Suwon 440-746, Korea Manuscript 2Center for Superfunctional Materials, Department of Chemistry, Ulsan Institute of Science and Technology (UNIST), Ulsan 689-798, Korea *Corresponding authors, [email protected] , [email protected] Accepted Abstract We have studied geometries, energies and vibrational spectra of disulfuric acid - (H 2S2O7) and its anion (HS 2O7 ) hydrated by a few water molecules, using density functional theory (M062X) and ab initio theory (SCS-MP2 and CCSD(T)). -
"Fluorine Compounds, Organic," In: Ullmann's Encyclopedia Of
Article No : a11_349 Fluorine Compounds, Organic GU¨ NTER SIEGEMUND, Hoechst Aktiengesellschaft, Frankfurt, Federal Republic of Germany WERNER SCHWERTFEGER, Hoechst Aktiengesellschaft, Frankfurt, Federal Republic of Germany ANDREW FEIRING, E. I. DuPont de Nemours & Co., Wilmington, Delaware, United States BRUCE SMART, E. I. DuPont de Nemours & Co., Wilmington, Delaware, United States FRED BEHR, Minnesota Mining and Manufacturing Company, St. Paul, Minnesota, United States HERWARD VOGEL, Minnesota Mining and Manufacturing Company, St. Paul, Minnesota, United States BLAINE MCKUSICK, E. I. DuPont de Nemours & Co., Wilmington, Delaware, United States 1. Introduction....................... 444 8. Fluorinated Carboxylic Acids and 2. Production Processes ................ 445 Fluorinated Alkanesulfonic Acids ...... 470 2.1. Substitution of Hydrogen............. 445 8.1. Fluorinated Carboxylic Acids ......... 470 2.2. Halogen – Fluorine Exchange ......... 446 8.1.1. Fluorinated Acetic Acids .............. 470 2.3. Synthesis from Fluorinated Synthons ... 447 8.1.2. Long-Chain Perfluorocarboxylic Acids .... 470 2.4. Addition of Hydrogen Fluoride to 8.1.3. Fluorinated Dicarboxylic Acids ......... 472 Unsaturated Bonds ................. 447 8.1.4. Tetrafluoroethylene – Perfluorovinyl Ether 2.5. Miscellaneous Methods .............. 447 Copolymers with Carboxylic Acid Groups . 472 2.6. Purification and Analysis ............. 447 8.2. Fluorinated Alkanesulfonic Acids ...... 472 3. Fluorinated Alkanes................. 448 8.2.1. Perfluoroalkanesulfonic Acids -
Arsine Back up Data Report
NIOSH Manual of Analytical Methods (NMAM) 5th Edition BACKUP DATA REPORT NIOSH Method No. 6001 Title: Arsine Analyte: Arsine Author/developer: Developed under contract Date: 1976 Note: Method 6001 is a combination of two older, previously published methods: S229 and P&CAM 265. Therefore, the backup data report is a combination of the two methods’ reports. The backup data report for method S229 is a regular written report. The backup data report for P&CAM 265, however, is in the form of a published journal article. The written report for S229 follows, the journal article for P&CAM can be seen here as a pdf. Disclaimer: Mention of any company or product does not constitute endorsement by the National Institute for Occupational Safety and Health, Centers for Disease Control and Prevention. In addition, citations to websites external to NIOSH do not constitute NIOSH endorsement of the sponsoring organizations or their programs or products. Furthermore, NIOSH is not responsible for the content of these websites. All web addresses referenced in this document were accessible as of the publication date. NIOSH Manual of Analytical Methods (NMAM), Fifth Edition Backup Data Report Method S229 Substance: Arsine OSHA Standard: 0.2 mg/m3 Chemical Used: Arsine in Nitrogen (14 ppm), Linde Specialty Gases Procedure The general procedure used is described in NIOSH Method 6001. The collection method has been adapted from P&CAM 127. The charcoal used was Lot 105 activated coconut charcoal supplied by SKC, Inc., Pittsburgh, PA. Desorption efficiency tests have not been carried out because the low concentration of the arsine source would require that large volumes of gas (200-800 ml) had to be injected directly into the charcoal tube. -
P – Block Elements SYJC
P – Block Elements Introduction The p-block elements are placed in groups 13 – 18 . The general electronic configuration is ns 2 np1 – 6. The groups included in the syllabus are 15, 16, 17 and 18. Group 15 Elements Nitrogen family: configuration is ns2np3. The elements of group 15 – nitrogen (N), phosphorus (P), arsenic (As), antimony (Sb) bismuth (Bi) All Group 15 Elements tend to follow the general periodic trends: Periodic properties Trends Electronegativity:(the atom's ability of Decreases down the group attracting electrons) Ionization Enthalpy (the amount of decreases energy required to remove an electron from the atom in it's gaseous phase) Atomic Radii (the radius of the atom) increases Electron Affinity (ability of the atom to decreases accept an electron) Melting Point (amount of energy increases going down the required to break bonds to change a group solid phase substance to a liquid phase) Boiling Point (amount of energy increases going down the required to break bonds to change a group liquid phase substance to a gas) Chemical properties Action of air;(high temp arc) N2 + O2 2NO Action oxidizing agents: P4 +20HNO3 4H3PO4 + 20 NO2+4 H20 As4 + 20 HNO3 4H3AsO4 + 20 NO2+4 H20 Action of hot conc H2SO4 P4 +10 H2SO4 4H3PO4 + 10 SO2+4 H20 As4 +10 H2SO4 4H3AsO4 + 4 Sb + 6 H2SO4 Sb2(SO4)3 + 3 Hydrides All form hydrides with formula EH3 ( E = N, P, As, Sb , Bi) oxidation state = – 3 Hydrogen bonding in NH3 The stability of hydrides decrease down the group due to decrease in bond Hydrides comparison Anomalous behaviour of -
Interhalogen Compounds
INTERHALOGEN COMPOUNDS Smt. EDNA RICHARD Asst. Professor Department of Chemistry INTERHALOGEN COMPOUND An interhalogen compound is a molecule which contains two or more different halogen atoms (fluorine, chlorine, bromine, iodine, or astatine) and no atoms of elements from any other group. Most interhalogen compounds known are binary (composed of only two distinct elements) The common interhalogen compounds include Chlorine monofluoride, bromine trifluoride, iodine pentafluoride, iodine heptafluoride, etc Interhalogen compounds into four types, depending on the number of atoms in the particle. They are as follows: XY XY3 XY5 XY7 X is the bigger (or) less electronegative halogen. Y represents the smaller (or) more electronegative halogen. Properties of Interhalogen Compounds •We can find Interhalogen compounds in vapour, solid or fluid state. • A lot of these compounds are unstable solids or fluids at 298K. A few other compounds are gases as well. As an example, chlorine monofluoride is a gas. On the other hand, bromine trifluoride and iodine trifluoride are solid and liquid respectively. •These compounds are covalent in nature. •These interhalogen compounds are diamagnetic in nature. This is because they have bond pairs and lone pairs. •Interhalogen compounds are very reactive. One exception to this is fluorine. This is because the A-X bond in interhalogens is much weaker than the X-X bond in halogens, except for the F-F bond. •We can use the VSEPR theory to explain the unique structure of these interhalogens. In chlorine trifluoride, the central atom is that of chlorine. It has seven electrons in its outermost valence shell. Three of these electrons form three bond pairs with three fluorine molecules leaving four electrons. -
Kinetics and Mechanism of Oxidation of Glycine and Alanine by Oxone R
http://dx.doi.org/10.5935/0103-5053.20140139 J. Braz. Chem. Soc., Vol. 25, No. 9, 1545-1551, 2014. Printed in Brazil - ©2014 Sociedade Brasileira de Química Article 0103 - 5053 $6.00+0.00 A Kinetics and Mechanism of Oxidation of Glycine and Alanine by Oxone® Catalyzed by Bromide Ion Malharrao R. Thombare and Gavisiddappa S. Gokavi* Kinetics and Catalysis Laboratory, Department of Chemistry, Shivaji University, 416004 Kolhapur, India A oxidação da glicina e alanina por Oxone®, catalisada por íons brometo foi estudada em meio ácido. A reação é iniciada pela oxidação do brometo ao bromo, que reage com o aminoácido. A formação de bromo é comprovada pelo exame espectrofotométrico da mistura reacional. O intermediário proposto envolve a formação de um complexo entre o bromo e o ânion do aminoácido. A taxa de reação é inibida por um aumento na concentração do íon hidrogênio devido ao equilíbrio de protonação dos aminoácidos. Um mecanismo é proposto e a lei da razão derivada foi verificada graficamente. O efeito da permissividade relativa, força iônica e temperatura também foram acompanhados e esses efeitos também dão suporte ao mecanismo proposto. Oxidation of glycine and alanine by Oxone® catalysed by bromide ions has been studied in acidic medium. The reaction is initiated by the oxidation of bromide to bromine, which then reacts with the amino acid. The formation of bromine is supported by the spectrophotometric examination of the reaction mixture. The proposed intermediate involves a complex formation between bromine and the anion of the amino acid. The rate of the reaction is inhibited by an increase in the hydrogen ion concentration due to the protonation equilibria of the amino acids.