4. CHEMICAL, PHYSICAL, and RADIOLOGICAL INFORMATION
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Table 2.Iii.1. Fissionable Isotopes1
FISSIONABLE ISOTOPES Charles P. Blair Last revised: 2012 “While several isotopes are theoretically fissionable, RANNSAD defines fissionable isotopes as either uranium-233 or 235; plutonium 238, 239, 240, 241, or 242, or Americium-241. See, Ackerman, Asal, Bale, Blair and Rethemeyer, Anatomizing Radiological and Nuclear Non-State Adversaries: Identifying the Adversary, p. 99-101, footnote #10, TABLE 2.III.1. FISSIONABLE ISOTOPES1 Isotope Availability Possible Fission Bare Critical Weapon-types mass2 Uranium-233 MEDIUM: DOE reportedly stores Gun-type or implosion-type 15 kg more than one metric ton of U- 233.3 Uranium-235 HIGH: As of 2007, 1700 metric Gun-type or implosion-type 50 kg tons of HEU existed globally, in both civilian and military stocks.4 Plutonium- HIGH: A separated global stock of Implosion 10 kg 238 plutonium, both civilian and military, of over 500 tons.5 Implosion 10 kg Plutonium- Produced in military and civilian 239 reactor fuels. Typically, reactor Plutonium- grade plutonium (RGP) consists Implosion 40 kg 240 of roughly 60 percent plutonium- Plutonium- 239, 25 percent plutonium-240, Implosion 10-13 kg nine percent plutonium-241, five 241 percent plutonium-242 and one Plutonium- percent plutonium-2386 (these Implosion 89 -100 kg 242 percentages are influenced by how long the fuel is irradiated in the reactor).7 1 This table is drawn, in part, from Charles P. Blair, “Jihadists and Nuclear Weapons,” in Gary A. Ackerman and Jeremy Tamsett, ed., Jihadists and Weapons of Mass Destruction: A Growing Threat (New York: Taylor and Francis, 2009), pp. 196-197. See also, David Albright N 2 “Bare critical mass” refers to the absence of an initiator or a reflector. -
Retention Indices for Frequently Reported Compounds of Plant Essential Oils
Retention Indices for Frequently Reported Compounds of Plant Essential Oils V. I. Babushok,a) P. J. Linstrom, and I. G. Zenkevichb) National Institute of Standards and Technology, Gaithersburg, Maryland 20899, USA (Received 1 August 2011; accepted 27 September 2011; published online 29 November 2011) Gas chromatographic retention indices were evaluated for 505 frequently reported plant essential oil components using a large retention index database. Retention data are presented for three types of commonly used stationary phases: dimethyl silicone (nonpolar), dimethyl sili- cone with 5% phenyl groups (slightly polar), and polyethylene glycol (polar) stationary phases. The evaluations are based on the treatment of multiple measurements with the number of data records ranging from about 5 to 800 per compound. Data analysis was limited to temperature programmed conditions. The data reported include the average and median values of retention index with standard deviations and confidence intervals. VC 2011 by the U.S. Secretary of Commerce on behalf of the United States. All rights reserved. [doi:10.1063/1.3653552] Key words: essential oils; gas chromatography; Kova´ts indices; linear indices; retention indices; identification; flavor; olfaction. CONTENTS 1. Introduction The practical applications of plant essential oils are very 1. Introduction................................ 1 diverse. They are used for the production of food, drugs, per- fumes, aromatherapy, and many other applications.1–4 The 2. Retention Indices ........................... 2 need for identification of essential oil components ranges 3. Retention Data Presentation and Discussion . 2 from product quality control to basic research. The identifi- 4. Summary.................................. 45 cation of unknown compounds remains a complex problem, in spite of great progress made in analytical techniques over 5. -
An Introduction to Isotopic Calculations John M
An Introduction to Isotopic Calculations John M. Hayes ([email protected]) Woods Hole Oceanographic Institution, Woods Hole, MA 02543, USA, 30 September 2004 Abstract. These notes provide an introduction to: termed isotope effects. As a result of such effects, the • Methods for the expression of isotopic abundances, natural abundances of the stable isotopes of practically • Isotopic mass balances, and all elements involved in low-temperature geochemical • Isotope effects and their consequences in open and (< 200°C) and biological processes are not precisely con- closed systems. stant. Taking carbon as an example, the range of interest is roughly 0.00998 ≤ 13F ≤ 0.01121. Within that range, Notation. Absolute abundances of isotopes are com- differences as small as 0.00001 can provide information monly reported in terms of atom percent. For example, about the source of the carbon and about processes in 13 13 12 13 atom percent C = [ C/( C + C)]100 (1) which the carbon has participated. A closely related term is the fractional abundance The delta notation. Because the interesting isotopic 13 13 fractional abundance of C ≡ F differences between natural samples usually occur at and 13F = 13C/(12C + 13C) (2) beyond the third significant figure of the isotope ratio, it has become conventional to express isotopic abundances These variables deserve attention because they provide using a differential notation. To provide a concrete the only basis for perfectly accurate mass balances. example, it is far easier to say – and to remember – that Isotope ratios are also measures of the absolute abun- the isotope ratios of samples A and B differ by one part dance of isotopes; they are usually arranged so that the per thousand than to say that sample A has 0.3663 %15N more abundant isotope appears in the denominator and sample B has 0.3659 %15N. -
CAS REGISTRY: Finding CAS Registry Numbers
STN® Quick Reference Card CAS REGISTRYSM: Finding CAS Registry Numbers® When you know the Substance Name Field Use Example /CN Use when you know the complete => E BENZOIC ACID/CN Chemical substance name. EXPAND first to => E “BICYCLO(2.2.1)HEPTANE”/CN Name determine if the name is in the database. Basic Index Use when you know segments of the => S FLUOROMETHYL name or don’t know how the name => S “2,2’” (W) BIPYRID? segments go together. => S PYRIDINE (XW) DICARBOXY? /CNS Use when you want to search for a => S ?MYCIN?/CNS Chemical Name character string embedded in a trade => S ?QUAT/CNS Segments name. Use left and right truncation to search for an embedded character string. Use when you want to require that a => S CHLOROPHENYL/CNS name segment is not part of a larger => S HEXANEDIOIC (XW) segment. DIMETHYL/CNS /HP Use when you want to restrict the search => S 1-PROPANOL/HP Heading to a Heading Parent from a CA index => S 2-PYRIDINECARBO?/HP Parent name. /INS.HP Use when you want to restrict the search => S (PYRIDINE (XW) Index Name to name segments from the Heading CARBONITRIL?)/INS.HP part of a CA index name. Segments - Parent => S FLUOROMETHYL/INS.HP Heading Parent /INS.NHP Use when you want to restrict the search => S MORPHOL?/INS.NHP Index Name to name segments from the non- => S FLUOROMETHYL/INS.NHP Segments - part of a CA index Heading-Parent Non-Heading name. Parent /ONS Use when you want to restrict the search => S VINCAM?/ONS Other Name to name segments from names other => S (INDOLE(XW)AMIN?)/ONS Segments than CA index names such as semi- systematic names, trade names, common names, etc. -
REGISTRY Database Summary Sheet (DBSS)
SM REGISTRY/ZREGISTRY (CAS REGISTRY ) Subject • All types of inorganic and organic substances, including alloys, coordination Coverage compounds, minerals, mixtures, polymers, salts, high throughput screening (HTS) compounds as well as nucleic acid and protein sequences • Substances included in REGISTRY meet the following criteria: - Identified by CAS as coming from a reputable source, including but not limited to patents, journals, chemical catalogs, and selected substance collections on the web - Described in largely unambiguous terms - Characterized by physical methods or described in a patent document example or claim - Consistent with the laws of atomic covalent organization • Experimental and predicted property data and tags and spectra data File Type Numeric, Structure Features Alerts (SDIs) Biweekly In addition, SMARTracker, an automatic crossfile current-awareness search, (SDI XFILE) using a REGISTRY search profile in CA, HCA, ZCA, CAplus, HCAplus or ZCAplus may be run weekly or biweekly (weekly is the default). CAS Registry Keep & Share SLART Number® Identifiers ® Learning Database STN Easy Structures Record • CAS Registry Numbers • Experimental and predicted property Content • CA index names and commonly used data and tags chemical names and trade names • Spectra • Molecular formulas • List of databases and regulatory listings • Structure diagrams containing information on the substances • Sequence data • Super roles and document type SM • Alloy composition tables information from CAplus • Classes for polymers • Displayable information for 10 most recent references for substances • Ring analysis data File Size More than 140 million organic and inorganic substances; more than 71.1 million sequences (4/18) Coverage Early 1800s to the present Updates Daily Language English Database Chemical Abstracts Service Producer 2540 Olentangy River Road P.O. -
Toxicological Profile for Plutonium
PLUTONIUM 1 1. PUBLIC HEALTH STATEMENT This public health statement tells you about plutonium and the effects of exposure to it. The Environmental Protection Agency (EPA) identifies the most serious hazardous waste sites in the nation. These sites are then placed on the National Priorities List (NPL) and are targeted for long-term federal clean-up activities. Plutonium has been found in at least 16 of the 1,689 current or former NPL sites. Although the total number of NPL sites evaluated for this substance is not known, strict regulations make it unlikely that the number of sites at which plutonium is found would increase in the future as more sites are evaluated. This information is important because these sites may be sources of exposure and exposure to this substance may be harmful. When a substance is released from a large area, such as an industrial plant, or from a container, such as a drum or bottle, it enters the environment. This release does not always lead to exposure. You are normally exposed to a substance only when you come in contact with it. You may be exposed by breathing, eating, or drinking the substance, or by skin contact. However, since plutonium is radioactive, you can also be exposed to its radiation if you are near it. External exposure to radiation may occur from natural or man-made sources. Naturally occurring sources of radiation are cosmic radiation from space or radioactive materials in soil or building materials. Man- made sources of radioactive materials are found in consumer products, industrial equipment, atom bomb fallout, and to a smaller extent from hospital waste and nuclear reactors. -
Chromium-Nickel Steels Depleted of Nickel Stable Isotope Ni-58 As a Material for Fast Reactor Claddings
IAEA-CN-114/15p Chromium-Nickel steels depleted of nickel stable isotope Ni-58 as a material for fast reactor claddings G.L.Khorasanov, A.P.Ivanov, A.I.Blokhin, N.A.Demin Institute of Physics and Power Engineering named after A.I.Leypunsky 1, Bondarenko square, Obninsk, Kaluga region, 249033 Russia Tel.: +7-08439-98505, Fax: +7-095-2302326, E-mail: [email protected] INTRODUCTION Presently, the creation of new materials for fast reactor (FR) claddings is one of the main tasks of the nuclear engineering [1]. Now the Russian austenitic steel grade TchS68 with 15 % of nickel content is used as a material for the Russian FR BN-600 claddings [2]. With such a cladding the BN-600 fuel rod is stably operating during 10 years up to the fuel burn-up fraction of 10 % of heavy atoms (h.a.). The cladding material becomes swelled and unfit for further service after the fuel burn-up fraction of 10 % h.a. The task of increasing the fuel burn-up fraction up to 14 % h.a. is now the principal one for the BN-600 operation. For this purpose the new radiation–resistant austenitic steel grade EK164 with 19 % of nickel content is now developing in the Bochvar Institute, Russia [3]. It is generally assumed that steel swelling is caused by the combined action of radiation damage and helium accumulation in the irradiated material. In this case, nickel stable isotope, Ni-58 (its content in natural nickel is equal to 68%) is a source of helium creation. After 4 neutron capture via (n,g) reaction, Ni-58 is transmuted to radioisotope Ni-59 (T1/2=7.6⋅10 years) which has a high value of (n,α) reaction cross-section for thermal and epithermal neutrons. -
Lithium Isotope Fractionation During Uptake by Gibbsite
Available online at www.sciencedirect.com ScienceDirect Geochimica et Cosmochimica Acta 168 (2015) 133–150 www.elsevier.com/locate/gca Lithium isotope fractionation during uptake by gibbsite Josh Wimpenny a,⇑, Christopher A. Colla a, Ping Yu b, Qing-Zhu Yin a, James R. Rustad a, William H. Casey a,c a Department of Earth and Planetary Sciences, University of California, One Shields Avenue, Davis, CA 95616, United States b The Keck NMR Facility, University of California, One Shields Avenue, Davis, CA 95616, United States c Department of Chemistry, University of California, One Shields Avenue, Davis, CA 95616, United States Received 5 November 2014; accepted in revised form 8 July 2015; available online 15 July 2015 Abstract The intercalation of lithium from solution into the six-membered l2-oxo rings on the basal planes of gibbsite is well-constrained chemically. The product is a lithiated layered-double hydroxide solid that forms via in situ phase change. The reaction has well established kinetics and is associated with a distinct swelling of the gibbsite as counter ions enter the interlayer to balance the charge of lithiation. Lithium reacts to fill a fixed and well identifiable crystallographic site and has no solvation waters. Our lithium-isotope data shows that 6Li is favored during this intercalation and that the À À solid-solution fractionation depends on temperature, electrolyte concentration and counter ion identity (whether Cl ,NO3 À or ClO4 ). We find that the amount of isotopic fractionation between solid and solution (DLisolid-solution) varies with the amount of lithium taken up into the gibbsite structure, which itself depends upon the extent of conversion and also varies À À À with electrolyte concentration and in the counter ion in the order: ClO4 <NO3 <Cl . -
Chemical Name Federal P Code CAS Registry Number Acutely
Acutely / Extremely Hazardous Waste List Federal P CAS Registry Acutely / Extremely Chemical Name Code Number Hazardous 4,7-Methano-1H-indene, 1,4,5,6,7,8,8-heptachloro-3a,4,7,7a-tetrahydro- P059 76-44-8 Acutely Hazardous 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide P050 115-29-7 Acutely Hazardous Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]- P197 17702-57-7 Acutely Hazardous 1-(o-Chlorophenyl)thiourea P026 5344-82-1 Acutely Hazardous 1-(o-Chlorophenyl)thiourea 5344-82-1 Extremely Hazardous 1,1,1-Trichloro-2, -bis(p-methoxyphenyl)ethane Extremely Hazardous 1,1a,2,2,3,3a,4,5,5,5a,5b,6-Dodecachlorooctahydro-1,3,4-metheno-1H-cyclobuta (cd) pentalene, Dechlorane Extremely Hazardous 1,1a,3,3a,4,5,5,5a,5b,6-Decachloro--octahydro-1,2,4-metheno-2H-cyclobuta (cd) pentalen-2- one, chlorecone Extremely Hazardous 1,1-Dimethylhydrazine 57-14-7 Extremely Hazardous 1,2,3,4,10,10-Hexachloro-6,7-epoxy-1,4,4,4a,5,6,7,8,8a-octahydro-1,4-endo-endo-5,8- dimethanonaph-thalene Extremely Hazardous 1,2,3-Propanetriol, trinitrate P081 55-63-0 Acutely Hazardous 1,2,3-Propanetriol, trinitrate 55-63-0 Extremely Hazardous 1,2,4,5,6,7,8,8-Octachloro-4,7-methano-3a,4,7,7a-tetra- hydro- indane Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]- 51-43-4 Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, P042 51-43-4 Acutely Hazardous 1,2-Dibromo-3-chloropropane 96-12-8 Extremely Hazardous 1,2-Propylenimine P067 75-55-8 Acutely Hazardous 1,2-Propylenimine 75-55-8 Extremely Hazardous 1,3,4,5,6,7,8,8-Octachloro-1,3,3a,4,7,7a-hexahydro-4,7-methanoisobenzofuran Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime 26419-73-8 Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime. -
Oxidation State Slides.Key
Oxidation States Dr. Sobers’ Lecture Slides The Oxidation State Also known as the oxidation number The oxidation state is used to determine whether an element has been oxidized or reduced. The oxidation state is not always a real, quantitative, physical constant. The oxidation state can be the charge on an atom: 2+ - MgCl2 Mg Cl Oxidation State: +2 -1 2 The Oxidation State For covalently bonded substances, it is not as simple as an ionic charge. A covalent bond is a sharing of electrons. The electrons are associated with more than one atomic nuclei. This holds the nuclei together. The electrons may not be equally shared. This creates a polar bond. The electronegativity of a covalently bonded atom is its ability to attract electrons towards itself. 3 Example: Chlorine Sodium chloride is an ionic compound. In sodium chloride, the chloride ion has a charge and an oxidation state of -1. The oxidation state of sodium is +1. 4 Example: Chlorine In a chlorine molecule, the chlorine atoms are covalently bonded. The two atoms share electrons equally and the oxidation state is 0. 5 Example: Chlorine The two atoms of a hydrogen chloride molecule are covalently bonded. The electrons are not shared equally because chlorine is more electronegative than hydrogen. There are no ions but the oxidation state of chlorine in HCl is -1 and the oxidation state of hydrogen is +1. 6 7 Assigning Oxidation States See the handout for the list of rules. Rule 1: Free Elements Free elements have an oxidation state of zero Example Oxidation State O2(g) 0 Fe(s) 0 O3(g) 0 C(graphite) 0 C(diamond) 0 9 Rule 2: Monatomic Ions The oxidation state of monatomic ions is the charge of the ion Example Oxidation State O2- -2 Fe3+ +3 Na+ +1 I- -1 V4+ +4 10 Rule 3: Fluorine in Compounds Fluorine in a compound always has an oxidation state of -1 Example Comments and Oxidation States NaF These are monatomic ions. -
Structure-Property Relationships of Layered Oxypnictides
AN ABSTRACT OF THE DISSERTATION OF Sean W. Muir for the degree of Doctor of Philosophy in Chemistry presented on April 17, 2012. Title: Structure-property Relationships of Layered Oxypnictides Abstract approved:______________________________________________________ M. A. Subramanian Investigating the structure-property relationships of solid state materials can help improve many of the materials we use each day in life. It can also lead to the discovery of materials with interesting and unforeseen properties. In this work the structure property relationships of newly discovered layered oxypnictide phases are presented and discussed. There has generally been worldwide interest in layered oxypnictide materials following the discovery of superconductivity up to 55 K for iron arsenides such as LnFeAsO1-xFx (where Ln = Lanthanoid). This work presents efforts to understand the structure and physical property changes which occur to LnFeAsO materials when Fe is replaced with Rh or Ir and when As is replaced with Sb. As part of this work the solid solution between LaFeAsO and LaRhAsO was examined and superconductivity is observed for low Rh content with a maximum critical temperature of 16 K. LnRhAsO and LnIrAsO compositions are found to be metallic; however Ce based compositions display a resistivity temperature dependence which is typical of Kondo lattice materials. At low temperatures a sudden drop in resistivity occurs for both CeRhAsO and CeIrAsO compositions and this drop coincides with an antiferromagnetic transition. The Kondo scattering temperatures and magnetic transition temperatures observed for these materials can be rationalized by considering the expected difference in N(EF)J parameters between them, where N(EF) is the density of states at the Fermi level and J represents the exchange interaction between the Ce 4f1 electrons and the conduction electrons. -
Chair's Message Making Chemical Testing Relevant to Breast Cancer
Newsletter February 2011 Santa Clara Valley Section American Chemical Society Volume 33 No. 2 FEBRUARY 2011 NEWSLETTER TOPICS March Dinner Meeting • March Dinner Meeting: Making Making Chemical Testing Chemical Testing Relevant to Breast Cancer Relevant to Breast Cancer • Chair’s Message Dr. Megan R. Schwarzman • February Dinner Meeting: Sex, Love Abstract ductive environmental health, and Oxytocin Although breast cancer is U.S. and European chemicals one of the leading causes of can- policy, and the implications for • Welcome to the Santa Clara Valley cer and death in women, even human health and the environ- Section of ACS the small numbers of chemicals ment of the production, use and • New Members List for December that undergo safety testing are disposal of chemicals and prod- • Volunteer with Kids and Chemistry not routinely evaluated for their ucts. She is a research scientist at impacts on mammary (breast) the Center for Occupational and • Black History Month tissue. Likewise, there is no well- Environmental Health (COEH), • Committee Chair Needed established set of tests for screen- in UC Berkeley’s School of Public • Albert Ghiorso, Nuclear Researcher ing chemicals for their ability to raise the risk Health, and Associate Director of Health and • SPLASH is Coming to Stanford of breast cancer. Environment for the interdisciplinary In 2010, Dr. Schwarzman served as continued on next page Principal Investigator of a project to tackle this Chair's Message issue. The Breast Cancer and Chemicals Policy project, supported by a grant from the March Dinner Meeting As I write this, California Breast Cancer Research Program, Joint Meeting with Palo Alto AWIS we’ve just experi- convened a panel of 20 scientists and policy enced a New Year experts to review the biological mechanisms Date: Wednesday, March 23, 2011 celebration and associated with breast cancer and propose a Time: 7:00 Networking Dinner jumped into the strategy for screening and identifying chemi- 7:30-7:45 Announcements International Year of cals that could increase the risk of the disease.