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Atmospheric Source Terms for the Idaho Chemical Processing Plant, 1957 – 1959
FINAL ATMOSPHERIC SOURCE TERMS FOR THE IDAHO CHEMICAL PROCESSING PLANT, 1957–1959 Contract No. 200-2002-00367 Task Order No. 1, Subtask 1 A final report to the Centers for Disease Control and Prevention Atlanta, Georgia 30335 SC&A, Inc. 6858 Old Dominion Drive, Suite 301 McLean, Virginia 22101 SENES Oak Ridge, Inc. 102 Donner Drive Oak Ridge, Tennessee 37830 Authors: Robert P. Wichner, SENES Oak Ridge, Inc. John-Paul Renier, SENES Oak Ridge, Inc. A. Iulian Apostoaei, SENES Oak Ridge, Inc. July 2005 ICPP Source Terms July 2005 TABLE OF CONTENTS EXECUTIVE SUMMARY .......................................................................................................ES-1 1.0 SCOPE AND APPROACH ............................................................................................. 1-1 1.1 Scope .................................................................................................................. 1-1 1.2 Approach.............................................................................................................. 1-1 1.2.1 Operational RaLa Releases ...................................................................... 1-1 1.2.2 Idaho Chemical Processing Plant Criticality Approach........................... 1-2 2.0 THE RADIOACTIVE LANTHANUM (RaLa) PROCESS ............................................ 2-1 2.1 Background .......................................................................................................... 2-1 2.1.1 Requirement ............................................................................................ -
Cross Section Data for the Production of the Positron Emitting Niobium Isotope 90Nb Via the 90Zr(P, N)-Reaction
Radiochim. Acta 90, 1–5 (2002) by Oldenbourg Wissenschaftsverlag, München Cross section data for the production of the positron emitting niobium isotope 90Nb via the 90Zr(p, n)-reaction By S. Busse1,2,F.Rösch1,∗ andS.M.Qaim2 1 Institut für Kernchemie, Johannes Gutenberg-Universität, D-55128 Mainz, Germany 2 Institut für Nuklearchemie, Forschungszentrum Jülich GmbH, D-52425 Jülich, Germany (Received April 19, 2001; accepted in revised form July 16, 2001) Positron emitter 90Nb / Nuclear reaction / (α, 3n)-reactions on natural yttrium. A medium-sized cy- Excitation function / Calculated integral yield / clotron would allow the production of 90Nb via the (p, n)-, Experimental thick target yield / Radionuclidic impurities (d, 2n)- or the (3He, 2n)-process. In fact even a small-sized cyclotron (Ep ≤ 16 MeV) should lead to sufficient quanti- ties of the radioisotope via the (p, n)-reaction. A few stud- Summary. The radioisotope 90Nb decays with a positron ies have shown that the (d, 2n)-reaction requires a deuteron + branching of 53% and a relatively low β -energy of energy of about 16 MeV [5–7], the (3He, 2n)-process a 3He- = . = . Emean 0 66 MeV and Emax 1 5 MeV. Its half-life of 14 6h energy of ≥ 30 MeV and the (α, 3n)-reaction an α-particle makes it especially promising for quantitative investigation energy of ≥ 45 MeV [8]. Furthermore, the systematics of of biological processes with slow distribution kinetics using (3He, 2n)- and (p, n)-reactions suggest that the production positron emission tomography. To optimise its production, 90 the excitation functions of 90Zr(p, xn)-processes were studied yield of Nb should be higher in the latter process. -
Determining Atomic Mass Practice with Answers
Determining Atomic Mass Practice with Answers Atomic Mass • Refers to the mass of an atom. • Number of protons and neutrons • Atoms are too small to mass so mass is determined by the relative mass of a standard atom. By international agreement (IUPAC), Carbon12 is the chosen standard atom because of its abundance here on Earth. Atomic Mass Unit defined is a mass exactly equal to 1/12th of one carbon12 atom. 1 carbon12 atom = 12 amu Determining Atomic Mass Practice with Answers Determine Atomic Mass Unit for Hydrogen Hydrogen 1 as 1 proton and 0 neutrons 1/12 = .0833 x 100 = 8.33% So hydrogen is 8.33% of one atom of Carbon12 Atomic Mass of Hydrogen = mass of 1 atom of Carbon 12 x 8.33% = 12 x .0833 =.9996 = 1.0 amu Through different methods of experimental testing, chemists have more accurately determined the mass of hydrogen to be 1.008, which is more like 8.40%. Determining Atomic Mass Practice with Answers Determining Average Atomic Mass: Because element's usually have more than one isotope, which means their masses are different an average must be determine to reflect the mass of all an atom's isotopes. Example: A sample of cesium is 75% Cs-133, 20% Cs-132, and 5% Cs-134. What is the average atomic mass? ANSWER: .75 x 133 = 99.75 .20 x 132 = 26.4 .05 x 134 = 6.7 Total = 132.85 amu average atomic mass unit Determining Atomic Mass Practice with Answers Isotopes and Average Atomic Mass Iodine: 80% 127 I 17% 126 I 3% 128 I ANSWER: .80 x 127 = 101.6 .17 x 126 = 21.42 .03 x 128 = 3.84 Total = 126.86 amu Determining Atomic Mass Practice with Answers Determining Atomic Mass Practice with Answers Determining Atomic Mass Practice with Answers Determining Atomic Mass Practice with Answers Determining Atomic Mass Practice with Answers Determining Atomic Mass Practice with Answers Determining Atomic Mass Practice with Answers Determining Atomic Mass Practice with Answers Determining Atomic Mass Practice with Answers Determining Atomic Mass Practice with Answers Bromine which exists as a dark, red gas is Br2. -
Isotopes of M&M-Ium
Name _________________________________________________________________ Hour __________________ Isotopes of m&m-ium Elements commonly exist with differing numbers of neutrons. We call these elements isotopes and an example is Bromine-79 and Bromine-81. These isotopes are naturally occurring…but do not exist equally in nature. Br-79 is more common and occurs 55% of the time while Br-81 occurs 45% of the time. To calculate the average atomic mass (the weighted average of the masses of its isotopes) of bromine you need to take into account the relative abundance of each element. The average atomic mass = (% abundance of isotope 1)x(mass of isotope 1) + (% abundance of isotope 2)x(mass of isotope 2) (% should be expressed in decimals) Pre-Lab Questions: 1. Calculate the average atomic mass of Bromine using the % abundances above: 2. Carbon has 2 stable isotopes: C-12 with a natural abundance of 98.89% and C-14 at 1.11%. Calculate the average atomic mass of Carbon. m&mium, a recently discovered element from the chocolate mountains of Wonkaland, exits as two isotopes. m&mium has many different colors and your job is to find the average atomic mass of one color of m&mium. Safety Precautions: Never eat anything that has touched lab equipment! Use a baking cup so your group can eat the m&ms when you are done! Procedure: Show all work for all calculations. 1. Record the number of small m&m’s and large m&m’s you have (your color only) in the table. 2. Record the total number of m&m’s you have. -
Discovery of the Bromium Isotopes
Discovery of the Bromium Isotopes J. Kathawa, J. Claes, M. Thoennessen∗ National Superconducting Cyclotron Laboratory and Department of Physics and Astronomy, Michigan State University, East Lansing, MI 48824, USA Abstract Twenty-eight bromium isotopes have so far been observed; the discovery of these isotopes is discussed. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented. ∗Corresponding author. Email address: [email protected] (M. Thoennessen) Preprint submitted to Atomic Data and Nuclear Data Tables April 28, 2010 Contents 1. Introduction . 2 2. Discovery of 70−97Br ................................................................................... 3 2.1. 70Br............................................................................................. 3 2.2. 71Br............................................................................................. 3 2.3. 72Br............................................................................................. 5 2.4. 73Br............................................................................................. 5 2.5. 74Br............................................................................................. 5 2.6. 75Br............................................................................................. 5 2.7. 76Br............................................................................................. 6 2.8. 77Br............................................................................................ -
Arxiv:1006.4033V2 [Nucl-Ex] 8 Sep 2010
Discovery of Calcium, Indium, Tin, and Platinum Isotopes S. Amos, J. L. Gross, M. Thoennessen∗ National Superconducting Cyclotron Laboratory and Department of Physics and Astronomy, Michigan State University, East Lansing, MI 48824, USA Abstract Currently, twenty-four calcium, thirty-eight indium, thirty-eight tin and thirty-nine platinum isotopes have been observed and the discovery of these isotopes is discussed here. For each isotope a brief synopsis of the first refereed publication, including the production and identification method, is presented. arXiv:1006.4033v2 [nucl-ex] 8 Sep 2010 ∗Corresponding author. Email address: [email protected] (M. Thoennessen) Preprint submitted to Atomic Data and Nuclear Data Tables November 1, 2018 Contents 1. Introduction . 4 2. Discovery of 35−58Ca ................................................................................... 5 2.1. 36Ca ............................................................................................ 5 2.2. 37Ca ............................................................................................ 7 2.3. 38Ca ............................................................................................ 7 2.4. 39Ca ............................................................................................ 7 2.5. 40Ca ............................................................................................ 7 2.6. 41Ca ............................................................................................ 8 2.7. 42;43Ca ......................................................................................... -
Arxiv:2006.05774V1 [Nucl-Ex] 10 Jun 2020 Bevddi Observed Aoaois Hl Ie,Cnd 0 1P0 K0J Canada River, Chalk Laboratories, Keywords: Pairs
Systematic reduction of the proton-removal cross section in neutron-rich medium-mass nuclei J. D´ıaz-Cort´esa, J. Benlliurea, J.L. Rodr´ıguez-S´ancheza, H. Alvarez-Pol´ a, T. Aumannb, C.A. Bertulanic, B. Blankd, E. Casarejosa,1, D. Cortina-Gila, D. Dragosavaca, V. F¨ohre, A. Garganof, M. Gasc´ona, W. Gawlikowiczh, A. Heinzi, K. Helariuttaj, A. Keli´c-Heile, S. Luki´ce, F. Montese,2, D. P´erez-Loureiroa,3, L. Pie´nkowskig, K-H. Schmidte, M. Stanioue, K. Suboti´ck, K. S¨ummerere, J. Taiebl, A. Trzci´nskag aIGFAE, Universidade de Santiago de Compostela, E-15782 Spain bInstitut f¨ur Kernphysik, Technische Universit¨at Darmstadt, 64289 Darmstadt, Germany cTexas A&M University-Commerce, 75428 Commerce, Texas, United States of America dCentre d’Etudes Nucleaires, F-33175 Bordeaux-Gradignan Cedex, France eGSI Helmholtzzentrum f¨ur Schwerionenforschung, D-64291 Darmstadt, Germany fIstituto Nazionale di Fisica Nucleare, Complesso Universitario di Monte S. Angelo, Via Cintia, I-80126 Napoli, Italy gHeavy Ion Laboratory, University of Warsaw, PL-02-093 Warsaw, Poland hCardinal Stefan Wyszynski University, PL-01-938 Warsaw, Poland iChalmers University of Technology, SE-41296 Gothenburg, Sweden jUniversity of Helsinki, FI-00014 Helsinki, Finland kInstitute of Nuclear Sciences Vinˇca, University of Belgrade, 11001 Belgrade, Serbia lCEA, DAM, DIF F-91297 Arpajon, France Abstract Single neutron- and proton-removal cross sections have been systematically measured for 72 medium-mass neutron- rich nuclei around Z=50 and energies around 900A MeV using the FRagment Separator (FRS) at GSI. Neutron- removal cross sections are described by considering the knock-out process together with initial- and final-state inter- actions. -
Radiation Therapy and Dosing Material Transport Methodology Robert O'brien University of Nevada, Las Vegas, [email protected]
UNLV Theses, Dissertations, Professional Papers, and Capstones 12-1-2016 Radiation Therapy and Dosing Material Transport Methodology Robert O'brien University of Nevada, Las Vegas, [email protected] Follow this and additional works at: https://digitalscholarship.unlv.edu/thesesdissertations Part of the Biomechanical Engineering Commons, Biomedical Commons, and the Biomedical Devices and Instrumentation Commons Repository Citation O'brien, Robert, "Radiation Therapy and Dosing Material Transport Methodology" (2016). UNLV Theses, Dissertations, Professional Papers, and Capstones. 2891. https://digitalscholarship.unlv.edu/thesesdissertations/2891 This Dissertation is brought to you for free and open access by Digital Scholarship@UNLV. It has been accepted for inclusion in UNLV Theses, Dissertations, Professional Papers, and Capstones by an authorized administrator of Digital Scholarship@UNLV. For more information, please contact [email protected]. RADIATION THERAPY AND DOSING MATERIAL TRANSPORT METHODOLOGY By Robert James O’Brien Master of Science, Materials and Nuclear Engineering University of Nevada, Las Vegas 2006 Bachelor of Science, Mechanical Engineering University of Nevada, Las Vegas 2005 Bachelor of Science, Applied Physics University of Nevada, Las Vegas 2005 A dissertation submitted in partial fulfillment of the requirements for the Doctor of Philosophy in Engineering – Mechanical Engineering Department of Mechanical Engineering Howard R. Hughes College of Engineering The Graduate College University of Nevada, Las Vegas December 2016 Copyright by Robert O’Brien, 2017 All Rights Reserved Dissertation Approval The Graduate College The University of Nevada, Las Vegas November 16, 2016 This dissertation prepared by Robert James O’Brien entitled Radiation Therapy and Dosing Material Transport Methodology is approved in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Engineering – Mechanical Engineering Department of Mechanical Engineering William Culbreth, Ph.D. -
A New Method of Pure 111In Production by Proton-Induced Nuclear Reactions with Enriched 112Sn 19 Consequently with Low Activity)
NUKLEONIKA 2007;52(1):17−27 ORIGINAL PAPER 111 A new method of pure In production Emil Bìták, Edward Rurarz, by proton-induced nuclear reactions Stefan Mikołajewski, with enriched 112Sn Jolanta Wojtkowska Abstract. We aimed at finding out a simple and reliable way of 111In production with the highest radionuclide purity from its grand parent 111Sb and parent 111Sn nuclei, produced by the 112Sn(p,2n)111Sb and 112Sn(p,pn)111Sn reactions, respectively. The target was a metallic 112Sn sample enriched to 84%. We have measured activation cross sections for seven reactions on an enriched 112Sn sample induced by 23.6 ± 0.8 MeV energy protons. Gamma-ray spectroscopy with 55 60 high-purity germanium detectors has been used. We also identified the activities of Co (T1/2 = 17.5 h) and Cu (T1/2 = 23.7 min) in proton beam monitoring Ni foils, induced in the natNi(p,X)55Co and natNi(p,X)60Cu reactions at 22.8 MeV proton energy. The cross sections determined for these reactions are: σ[natNi(p,X)55Co] = 36.6 ± 4 mb and σ[natNi(p,X)60Cu] = 64.4 ± 7 mb. The measured cross sections of reactions on tin isotopes are: σ[112Sn(p,n)112Sb] = 4 ± 0.8 mb; σ[112Sn(p,2n)111Sb] = 182 ± 26 mb; σ[112Sn(p,pn)111Sn] = 307 ± 35 mb; σ[114Sn(p,2n)113Sb] = 442 ± 52 mb; σ[117Sn(p,n)117Sb] = 15 ± 3 mb; σ[117Sn(p,p’γ)117mSn] = 0.37 ± 0.06 mb; σ[115Sn(p,2p)114m2In] = 0.01 ± 0.002 mb. -
Stdin (Ditroff)
50Ma02 The Hyper®ne Structure of the Stable Isotopes of Indium A. K. Mann, P. Kusch, Phys. Rev. 77, 427 (1950). 50Ma03 The Beta-Spectrum of Ca45 P. Macklin, L. Feldman, L. Lidofsky, C. S. Wu, Phys. Rev. 77, 137 (1950). 50Ma05 Study of Neodymium and Promethium Activities Induced by Neutron Irradiation of Neodymium J. A. Marinsky, L. E. Glendenin, NNES 9, 1264 (1950). 50Ma14 New Isotope of Neptunium L. B. Magnusson, S. G. Thompson, G. T. Seaborg, Phys. Rev. 78, 363 (1950). 50Ma15 The Fission Yield of Xe133 and Fine Structure in the Mass Yield Curve J. Macnamara, C. B. Collins, H. G. Thode, Phys. Rev. 78, 129(1950). 50Ma27 D. G. E. Martin, H. O. W. Richardson, Proc. Phys. Soc. (London) 63A, 223 (1950). 50Ma29 Neutron De®cient Isotopes of Iodine L. Marquez, I. Perlman, Phys. Rev. 78, 189 (1950). 50Ma50 A Table of Nuclear Moments, January 1950 J. E. Mack, Revs. Modern Phys. 22, 64 (1950). 50Ma65 R. Malm, W. W. Buechner, Phys. Rev. 80, 771 (1950). 50Ma76 The Natural Radioactivity of In115 E. A. Martell, W. F. Libby, Phys. Rev. 80, 977 (1950). 50Mc12 Radiation from Au197*(7x10-9 sec) F. K. McGowan, Phys. Rev. 78, 325A (1950). 50Mc22 Short-Lived Isomers F. K. McGowan, ORNL-694, p. 19 (1950). 50Mc60 A 5.7 x 10-9 sec Isomeric State in Ir191 F. K. McGowan, Phys. Rev. 79, 404 (1950). 50Mc64 A3x10-9 sec. Isomeric State in Eu153 F. K. McGowan, Phys. Rev. 80, 482 (1950). 50Mc79 A 1.7 x 10-9 sec Isomeric State in Er166 F. -
Discovery of the Selenium Isotopes
Discovery of the Selenium Isotopes J. Claes, J. Kathawa, M. Thoennessen∗ National Superconducting Cyclotron Laboratory and Department of Physics and Astronomy, Michigan State University, East Lansing, MI 48824, USA Abstract Thirty-one selenium isotopes have so far been observed; the discovery of these isotopes is discussed. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented. ∗Corresponding author. Email address: [email protected] (M. Thoennessen) Preprint submitted to Atomic Data and Nuclear Data Tables April 28, 2010 Contents 1. Introduction . 3 2. Discovery of 64−94Se.................................................................................... 3 2.1. 64Se............................................................................................. 3 2.2. 65Se............................................................................................. 3 2.3. 66Se............................................................................................. 5 2.4. 67Se............................................................................................. 5 2.5. 68Se............................................................................................. 5 2.6. 69Se............................................................................................. 5 2.7. 70Se............................................................................................. 5 2.8. 71Se............................................................................................ -
Stable Isotope Separation in Calutrons
Printed ill tho llnitzd Statss ot 4mcm 4vailsble frurii Nations' Technical Information Service U S :3ep?rtmelli uf Commerce 5285 Port 4oyal Cosd Spririizflald Viryinis 22161 NTlS ptwiodes P~III~~Copy ,498, Microfiche P,C1 I his rcpoti \*!is prspxed as an account of >,dSi-k sponsored by a3 agsncy of the United Sraies Governr;,ent. Neither thc !J nited Skiics i<n.~cti $IK~: nor any agency th2reof. no? any of thzir employoes, (ciakc?.Aijy ivarranty, express or irripiled, or assunias any legal liability or responsibility for ihe accuracy. compleienass, or usefulness of any inforriraiton. ;p ius, product, or process disclosed, or represents that its usewould not infr privately o-v?d ilghts Rcferencc herein to ai-y specific commercial product, process, or service by trade nziile, Zi'adei*lark, manufacturer, or otherwise, does not necsssarily constitute or imply its enduisemcat, recorn,n faVOiii-,g by ille United States(;ovc;riiiie!ii 01- any Zgency thereof Th opinions of auiihols cxp:essed here:!: d~ ~iui neccssarily statc or refisc?!host of the United Sta?ezGovernmer:?or any ngcncy therccf. ____ ___________... ..... .____ ORNL/TM-10356 OPERATIONS DIVISION STABLE ISOTOPE SEPARATION IN CALUTRONS: FORTY YEARS OF PRODUCTION AND DISTRIBUTION W. A. Bell J. G. Tracy Date Published: November 1987 Prepared by the OAK RIDGE NATIONAL LABORATORY Oak Ridge, Tennessee 37831 operated by MARTIN MARIETTA ENERGY SYSTEMS, INC. for the U.S. DEPARTMENT OF ENERGY under Contract No. DE-AC05-840R21400 iti CONTENTS Page ACKNOWLEDGMENTS ................................................. iv I. INTRODUCTION .............................................. 1 11. PROGRAM EVOLUTION ......................................... 1 111. RESEARCH AND DEVELOPMENT .................................. 5 IV. CHEMISTRY ................................................. 8 V.