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Heavy Element Chemistry Contractors' Meeting Program and Abstracts
Department of Energy Office of Science Chemical Sciences, Geosciences and Biosciences Division Heavy Element Chemistry Contractors' Meeting Advanced Photon Source Office Building Argonne National Laboratory November 19 - 21, 2000 Program and Abstracts Heavy Element Chemistry Contractors' Meeting November 19 - 21, 2000 Program i Sunday, November 19, 2000; 1630 - 2100 Put up posters in APS Office Building Gallery Monday Morning, November 20, 2000 700 - 900 Breakfast at the hotel; Poster set up in APS Office Building Gallery 900 Start of meeting - APS Office Building - E1100 and E1200 Department of Energy, Office of Science, Chemical 900 - 905 Edelstein, Norman Welcome and Introductions Sciences, Geosciences and Biosciences Division Department of Energy, Office The View of Heavy Element of Science, Chemical 905 - 930 Smith, Paul Chemistry from DOE, Sciences, Geosciences and Washington Biosciences Division 930 Short presentations - Oral session I - APS Office Building - E1100 and E1200 Gas Phase GAS-PHASE ACTINIDE ION Oak Ridge National 930 Gibson, John P1-1 CHEMISTRY Laboratory Chemistry Department, SUPERHEAVY ELEMENT University of California, CHEMISTRY STUDIES AT Berkeley, Nuclear Science 940 Nitsche, H. P1-2 THE BERKELEY GAS- Division, The Glenn T. FILLED SEPARATOR Seaborg Center, Lawrence Berkeley National Laboratory ii Solid State STRUCTURAL RELATIONSHIPS AND Dorhout, Peter UNIQUE ASPECTS OF Department of Chemistry, 950 P1-3 K. ACTINIDE Colorado State University CHALCOPHOSPHATE MATERIALS: Th, U, Pu. SPECTROSCOPIC INVESTIGATIONS OF Oak Ridge National 1000 Assefa, Z. P1-4 ACTINIDES IN THE SOLID Laboratory STATE SYNTHESIS AND PHOTOPHYSICS OF HEAVY Chemistry Division, Argonne 1010 Beitz, J. V. P1-5 ELEMENT-CONTAINING National Laboratory NANOPHASES ACTINIDE CHEMISTRY UNDER NEAR-NEUTRAL Los Alamos National 1020 Dewey, H. -
Thermal Transport in Thorium Dioxide Nuclear Engineering and Technology
Nuclear Engineering and Technology 50 (2018) 731e737 Contents lists available at ScienceDirect Nuclear Engineering and Technology journal homepage: www.elsevier.com/locate/net Original Article Thermal transport in thorium dioxide Jungkyu Park*, Eduardo B. Farfan, Christian Enriquez Kennesaw State University, Department of Mechanical Engineering, Kennesaw, GA 30144, USA article info abstract Article history: In this research paper, the thermal transport in thorium dioxide is investigated by using nonequilibrium Received 28 September 2017 molecular dynamics. The thermal conductivity of bulk thorium dioxide was measured to be 20.8 W/m-K, Received in revised form confirming reported values, and the phonon mean free path was estimated to be between 7 and 8.5 nm 20 December 2017 at 300 K. It was observed that the thermal conductivity of thorium dioxide shows a strong dependency Accepted 12 February 2018 on temperature; the highest thermal conductivity was estimated to be 77.3 W/m-K at 100 K, and the Available online 1 March 2018 lowest thermal conductivity was estimated to be 4.3 W/m-K at 1200 K. In addition, by simulating thorium dioxide structures with different lengths at different temperatures, it was identified that short Keywords: Molecular Dynamics Simulation wavelength phonons dominate thermal transport in thorium dioxide at high temperatures, resulting in Nuclear Fuel decreased intrinsic phonon mean free paths and minimal effect of boundary scattering while long Thermal Transport wavelength phonons dominate the thermal transport in thorium dioxide at low temperatures. Thorium Dioxide © 2018 Korean Nuclear Society, Published by Elsevier Korea LLC. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). -
The Development of the Periodic Table and Its Consequences Citation: J
Firenze University Press www.fupress.com/substantia The Development of the Periodic Table and its Consequences Citation: J. Emsley (2019) The Devel- opment of the Periodic Table and its Consequences. Substantia 3(2) Suppl. 5: 15-27. doi: 10.13128/Substantia-297 John Emsley Copyright: © 2019 J. Emsley. This is Alameda Lodge, 23a Alameda Road, Ampthill, MK45 2LA, UK an open access, peer-reviewed article E-mail: [email protected] published by Firenze University Press (http://www.fupress.com/substantia) and distributed under the terms of the Abstract. Chemistry is fortunate among the sciences in having an icon that is instant- Creative Commons Attribution License, ly recognisable around the world: the periodic table. The United Nations has deemed which permits unrestricted use, distri- 2019 to be the International Year of the Periodic Table, in commemoration of the 150th bution, and reproduction in any medi- anniversary of the first paper in which it appeared. That had been written by a Russian um, provided the original author and chemist, Dmitri Mendeleev, and was published in May 1869. Since then, there have source are credited. been many versions of the table, but one format has come to be the most widely used Data Availability Statement: All rel- and is to be seen everywhere. The route to this preferred form of the table makes an evant data are within the paper and its interesting story. Supporting Information files. Keywords. Periodic table, Mendeleev, Newlands, Deming, Seaborg. Competing Interests: The Author(s) declare(s) no conflict of interest. INTRODUCTION There are hundreds of periodic tables but the one that is widely repro- duced has the approval of the International Union of Pure and Applied Chemistry (IUPAC) and is shown in Fig.1. -
INFORMATION O a a .Aoi Chemistry-Traniuranie Elements
INFORMATION o a a .aoi Chemistry-Traniuranie Elements UNIVERSITY O r CALIFORNIA Radiation Laboratory Contract No. W-7405-eng~48 CUBSITIClTIOH CAKCBLUD IV. TT Ftv«Jbs Itti'.s fJ«cR'otsdLisV^ CRYSTAL STRUCTURES OF AMERICIUM COMPOUNDS D. H. Templeton and Carol H. Dauben February 3, 1953 RESTRICTEO^JCTA This document cqpm pLrw ricted data as defined in ttagSrarfic Energy Act of 1944. Its tsn fip rtfa l or disclosure of Its contents ^p*ny manner to an unautor- ised person is prohibited. Berkeley, California UNIVERSITY Of CALIFORNIA Rodiotiofl Loborotory 42RC8 Cover Shoot INDE X NO. Ill K£ ■ -10/ Do not rsrtovt Tbit document eo nto in t__ IL- pages Tbit is copy ^ of tor lot tL Glassification Eoch perton who rtcoivot thltdocument must tipn the cover thstt I Route to Notsd by Date Route to Noted by D aft OHO A im *[|S 5(M) CRYSTAL STRUCTURES OF AMERICIUM COMPOUNDS1 D. H. Templeton and Carol H. Dauben Department of Chemistry and Radiation Laboratory University of California, Berkeley, California February 3, 1953 ABSTRACT The crystal structures of several compounds of americium, element 95, have been determined by the X-ray powder diffraction method. AisF^ is hexagonal (LaF^ type) with a = 4. 067 t 0.001 X and c « 7. 225 t 0.002 Si for the pseudoceil which explains the powder data. AmO^ is cubic (CaF^ type) with 1 a = 5. 38) t 0.001 X AmOCl is tetragonal (PbFCl type) with a = 4.00+O.OlX, c = 6.78 t 0.01 X. The metal parameter la 0.18 t 0.01. -
Subject Index
SUBJECT INDEX Vol. 1: 1–698, Vol. 2: 699–1395, Vol. 3: 1397–2111, Vol. 4: 2113–2798, Vol. 5: 2799–3440. Page numbers suffixed by t and f refer to Tables and Figures respectively. Absorption spectra in aqueous solution, 752–770 of americium, 1364–1368 compounds of, 721–752 americium (III), 1364–1365, 1365f coordination complexes in solution, americium (IV), 1365 771–782 americium (V), 1366, 1367f history of, 699–700 americium (VI), 1366, 1367f isotope production, 702–703 americium (VII), 1367–1368, 1368f metallic state of, 717–721 of liquid plutonium, 963 in nature, 703–704 of neptunium, 763–766, 763f, 786–787 nuclear properties of, 700–702 neptunium (VII) ternary oxides, 729 separation and purification, 704–717 of plutonium plutonium hexafluoride, 1088, 1089f atomic properties of, 857–862 ions, 1113–1117, 1116t compounds of, 987–1108 plutonium (IV), 849 metal and intermetallic compounds of, polymerization, 1151, 1151f 862–987 tetrachloride, 1093–1094, 1094f natural occurrence of, 822–824 tribromide, 1099t, 1100 nuclear properties of, 815–822 trichloride, 1099, 1099t separation and purification of, 826–857 Accelerator mass spectrometry (AMS), of solution chemistry of, 1108–1203 neptunium, 790 Actinide elements Acetates atomic volumes of, 922–923, 923f of americium, 1322, 1323t extraction of of plutonium, 1177, 1180 DIDPA, 1276 Acetone, derived compounds, of americium, HDEHP, 1275 1322, 1323t, 1324 organophosphorus and Acids carbamoylphosphonate reagents, for Purex process, 711 1276–1278 for solvent extraction, 839 stripping of, 1280–1281 Actinide -
Techniques of Preparation and Crystal Chemistry of Transuranic Chalcogenides and Pnictides D
Techniques of preparation and crystal chemistry of transuranic chalcogenides and pnictides D. Damien, R. Haire, J. Peterson To cite this version: D. Damien, R. Haire, J. Peterson. Techniques of preparation and crystal chemistry of transuranic chalcogenides and pnictides. Journal de Physique Colloques, 1979, 40 (C4), pp.C4-95-C4-100. 10.1051/jphyscol:1979430. jpa-00218826 HAL Id: jpa-00218826 https://hal.archives-ouvertes.fr/jpa-00218826 Submitted on 1 Jan 1979 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. JOURNAL DE PHYSIQUE Colloque C4, supplément au n° 4, Tome 40, avril 1979, page C4-95 Techniques of preparation and crystal chemistry of transuranic chalcogenides and pnictides (*) D. A. Damien (**), R. G. Haire and J. R. Peterson (t) Transuranium Research Laboratory, Oak Ridge National Laboratory, Oak Ridge, TN 37830, U.S.A. Résumé. — La cristallochimie d'un certain nombre de chalcogénures et pnictures d'éléments transuraniens a été étudiée en utilisant les isotopes Am, Cm, Bk et Cf. Les composés ont été préparés par réaction directe du métal avec l'élément chalcogène ou pnictogène à température élevée. Les chalcogénures supérieurs ont été dissociés thermiquement pour donner des composés à stœchiométrie plus basse dont les sesquichalco- génures constituent la limite. -
Electrical Characterization of Crystalline UO 2 , Tho 2 and U
Air Force Institute of Technology AFIT Scholar Theses and Dissertations Student Graduate Works 12-17-2018 Electrical Characterization of Crystalline UO2, ThO2 AND U0.71Th0.29O2 Christina L. Dugan Follow this and additional works at: https://scholar.afit.edu/etd Part of the Engineering Physics Commons Recommended Citation Dugan, Christina L., "Electrical Characterization of Crystalline UO2, ThO2 AND U0.71Th0.29O2" (2018). Theses and Dissertations. 1944. https://scholar.afit.edu/etd/1944 This Dissertation is brought to you for free and open access by the Student Graduate Works at AFIT Scholar. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of AFIT Scholar. For more information, please contact [email protected]. ELECTRICAL CHARACTERIZATION OF CRYSTALLINE UO2, THO2 AND U0.71TH0.29O2 DISSERTATION Christina L. Dugan, Lieutenant Colonel, USA AFIT-ENP-DS-18-D-007 DEPARTMENT OF THE AIR FORCE AIR UNIVERSITY AIR FORCE INSTITUTE OF TECHNOLOGY Wright-Patterson Air Force Base, Ohio DISTRIBUTION STATEMENT A Approved For Public Release; Distribution Unlimited The views expressed in this thesis are those of the author and do not reflect the official policy or position of the United States Air Force, the Department of Defense, or the United States Government. AFIT-ENP-DS-18-D-007 ELECTRICAL CHARACTERIZATION OF CRYSTALLINE UO2, THO2 AND U0.71TH0.29O2 DISSERTATION Presented to the Faculty Department of Engineering Physics Graduate School of Engineering and Management Air Force Institute of Technology Air University Air Education and Training Command In Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy Christina L. -
Peaceful Berkelium
in your element Peaceful berkelium The first new element produced after the Second World War has led a rather peaceful life since entering the period table — until it became the target of those producing superheavy elements, as Andreas Trabesinger describes. f nomenclature were transitive, element 97 with the finding that in Bk(iii) compounds would be named after an Irish bishop spin–orbit coupling leads to a mixing of the Iwhose philosophical belief was that first excited state and the ground state. This material things do not exist. But between gives rise to unexpected electronic properties the immaterialist George Berkeley and the not present in analogous lanthanide element berkelium stands, of course, the structures containing terbium. Even more fine Californian city of Berkeley (pictured), recently5, a combined experimental and where the element was first produced in computational study revealed that berkelium December 1949. The city became the eponym can have stabilized +iii and +iV oxidation of element 97 “in a manner similar to that states also under mild aqueous conditions, used in naming its chemical homologue indicating a path to separating it from other terbium […] whose name was derived from lanthanides and actinides. the town of Ytterby, Sweden, where the rare The main use of berkelium, however — earth minerals were first found”1. arguably one that wouldn’t have met with A great honour for the city? The mayor Bishop Berkeley’s approval — remains a of Berkeley at the time reportedly displayed PHOTO STOCK / ALAMY AF ARCHIVE distinctly material one: as the target for “a complete lack of interest when he was the synthesis of other transuranium and called with the glad tidings”2. -
Upper Limit of the Periodic Table and the Future Superheavy Elements
CLASSROOM Rajarshi Ghosh Upper Limit of the Periodic Table and the Future Department of Chemistry The University of Burdwan ∗ Superheavy Elements Burdwan 713 104, India. Email: [email protected] Controversy surrounds the isolation and stability of the fu- ture transactinoid elements (after oganesson) in the periodic table. A single conclusion has not yet been drawn for the highest possible atomic number, though there are several the- oretical as well as experimental results regarding this. In this article, the scientific backgrounds of those upcoming super- heavy elements (SHE) and their proposed electronic charac- ters are briefly described. Introduction Totally 118 elements, starting from hydrogen (atomic number 1) to oganesson (atomic number 118) are accommodated in the mod- ern form of the periodic table comprising seven periods and eigh- teen groups. Total 92 natural elements (if technetium is consid- ered as natural) are there in the periodic table (up to uranium hav- ing atomic number 92). In the actinoid series, only four elements— Keywords actinium, thorium, protactinium and uranium—are natural. The Superheavy elements, actinoid rest of the eleven elements—from neptunium (atomic number 93) series, transactinoid elements, periodic table. to lawrencium (atomic number 103)—are synthetic. Elements after actinoids (i.e., from rutherfordium) are called transactinoid elements. These are also called superheavy elements (SHE) as they have very high atomic numbers. Prof. G T Seaborg had Elements after actinoids a very distinct contribution in the field of transuranium element (i.e., from synthesis. For this, Prof. Seaborg was awarded the Nobel Prize in rutherfordium) are called transactinoid elements. 1951. -
Plutonium and Americium Geochemistry at Hanford
Plutonium Futures: The Science 2014 Las Vegas, Nevada, USA 7-12 September 2014 ISBN: 978-1-5108-0808-9 Printed from e-media with permission by: Curran Associates, Inc. 57 Morehouse Lane Red Hook, NY 12571 Some format issues inherent in the e-media version may also appear in this print version. Copyright© (2014) by the American Nuclear Society All rights reserved. Printed by Curran Associates, Inc. (2015) For permission requests, please contact the American Nuclear Society at the address below. American Nuclear Society 555 North Kensington Avenue LaGrange Park, Illinois 60526 Phone: (800) 323-3044 (708) 352-6611 Fax: (708) 352-0499 www.ans.org Additional copies of this publication are available from: Curran Associates, Inc. 57 Morehouse Lane Red Hook, NY 12571 USA Phone: 845-758-0400 Fax: 845-758-2634 Email: [email protected] Web: www.proceedings.com Table of Contents MONDAY, SEPTEMBER 8, 2014, 8:00-10:20 A.M. MONDAY PLENARIES Session Chair: Kerri Blobaum (LLNL) 1Plutonium and Americium Geochemistry at Hanford A. R. Felmy, K. J. Cantrell, E. C. Buck (PNNL), S. D. Conradson (LANL), plenary 3Consequences of Electronic Correlations in Plutonium-Based Intermetallics J. D. Thompson, E. D. Bauer, G. Koutroulakis, J. N. Mitchell, A. M. Mounce, P. H. Tobash, H. Yasuoka (LANL), plenary MONDAY, SEPTEMBER 8, 2014, 10:40 A.M-12:00 P.M. CONDENSED MATTER PHYSICS—I Session Chair: Roberto Caciuffo (ITU) 5A Plutonium-Based Single-Molecule Magnet N. Magnani, E. Colineau, J.-C. Griveau, C. Apostolidis, O. Walter, R. Caciuffo (EC, JRC, Inst for Transuranium Elements), invited 6Quantum Criticality in PuMX5(M=Co, Rh; X=Ga, In) Superconductors Eric D. -
The Chemical Complexities of Plutonium David L
The Chemical Complexities of Plutonium David L. Clark ew people have ever seen plutonium, and far fewer have actually handled or manipu- lated it. Yet this manmade element has arguably altered the course of civilization as Fmuch as copper, bronze, iron, or steel. Within five years of its synthesis, the primary use of plutonium was for the release of nuclear energy in weapons of mass destruction, and it seemed that the new element might lead the human race to the brink of self-annihilation. But instead, plutonium has become a stabilizing agent in global politics, forcing the human race to govern itself without resorting to nuclear war. Never before has a simple chemical element had such a profound impact on the consciousness of mankind. Plutonium has had a similarly humbling impact in the more circumscribed arena of science. Incredibly, it displays physicochemical behaviors that are among the most complex of any element in the periodic table. The pure element exhibits seven distinct crystal phases, is highly reactive, and is known to form compounds, complexes, or alloys with virtually every other element. Molten plutonium is highly corrosive and will slowly react with its container, causing difficulties for handling. When elemental plutonium reacts to give up its valence electrons, it can form a wide variety of positively charged ions with the ability to form up to twelve chemical bonds to other ions or molecules in solution. The element can exhibit five oxidation states, and under certain chemical conditions, four different oxidation states can be present in appreciable amounts simultaneously! No other element displays such a complex chemistry. -
The Elements.Pdf
A Periodic Table of the Elements at Los Alamos National Laboratory Los Alamos National Laboratory's Chemistry Division Presents Periodic Table of the Elements A Resource for Elementary, Middle School, and High School Students Click an element for more information: Group** Period 1 18 IA VIIIA 1A 8A 1 2 13 14 15 16 17 2 1 H IIA IIIA IVA VA VIAVIIA He 1.008 2A 3A 4A 5A 6A 7A 4.003 3 4 5 6 7 8 9 10 2 Li Be B C N O F Ne 6.941 9.012 10.81 12.01 14.01 16.00 19.00 20.18 11 12 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 3 Na Mg IIIB IVB VB VIB VIIB ------- VIII IB IIB Al Si P S Cl Ar 22.99 24.31 3B 4B 5B 6B 7B ------- 1B 2B 26.98 28.09 30.97 32.07 35.45 39.95 ------- 8 ------- 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 4 K Ca Sc Ti V Cr Mn Fe Co Ni Cu Zn Ga Ge As Se Br Kr 39.10 40.08 44.96 47.88 50.94 52.00 54.94 55.85 58.47 58.69 63.55 65.39 69.72 72.59 74.92 78.96 79.90 83.80 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 5 Rb Sr Y Zr NbMo Tc Ru Rh PdAgCd In Sn Sb Te I Xe 85.47 87.62 88.91 91.22 92.91 95.94 (98) 101.1 102.9 106.4 107.9 112.4 114.8 118.7 121.8 127.6 126.9 131.3 55 56 57 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 6 Cs Ba La* Hf Ta W Re Os Ir Pt AuHg Tl Pb Bi Po At Rn 132.9 137.3 138.9 178.5 180.9 183.9 186.2 190.2 190.2 195.1 197.0 200.5 204.4 207.2 209.0 (210) (210) (222) 87 88 89 104 105 106 107 108 109 110 111 112 114 116 118 7 Fr Ra Ac~RfDb Sg Bh Hs Mt --- --- --- --- --- --- (223) (226) (227) (257) (260) (263) (262) (265) (266) () () () () () () http://pearl1.lanl.gov/periodic/ (1 of 3) [5/17/2001 4:06:20 PM] A Periodic Table of the Elements at Los Alamos National Laboratory 58 59 60 61 62 63 64 65 66 67 68 69 70 71 Lanthanide Series* Ce Pr NdPmSm Eu Gd TbDyHo Er TmYbLu 140.1 140.9 144.2 (147) 150.4 152.0 157.3 158.9 162.5 164.9 167.3 168.9 173.0 175.0 90 91 92 93 94 95 96 97 98 99 100 101 102 103 Actinide Series~ Th Pa U Np Pu AmCmBk Cf Es FmMdNo Lr 232.0 (231) (238) (237) (242) (243) (247) (247) (249) (254) (253) (256) (254) (257) ** Groups are noted by 3 notation conventions.