Appendix E: Radiation
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Measurements of Fission Cross Sections for the Isotopes Relevant to the Thorium Fuel Cycle
EUROPEAN ORGANIZATION FOR NUCLEAR RESEARCH CERN/INTC 2001-025 INTC/P-145 08 Aug 2001 Measurements of Fission Cross Sections for the Isotopes relevant to the Thorium Fuel Cycle The n_TOF Collaboration ABBONDANNO U.20, ANDRIAMONJE S.10, ANDRZEJEWSKI J.24, ANGELOPOULOS A.12, ASSIMAKOPOULOS P.15, BACRI C-O.8, BADUREK G.1, BAUMANN P.9, BEER H.11, BENLLIURE J.32, BERTHIER B.8, BONDARENKO I.26, BOS A.J.J.36, BUSTREO N.19, CALVINO F.33, CANO-OTT D.28, CAPOTE R.31, CARLSON P.34, CHARPAK G.5, CHAUVIN N.8, CENNINI P.5, CHEPEL V.25, COLONNA N.20, CORTES G.33, CORTINA D.32, CORVI F.23, DAMIANOGLOU D.16, DAVID S.8, DIMOVASILI E.12, DOMINGO C.29, DOROSHENKO A.27, DURAN ESCRIBANO I.32, ELEFTHERIADIS C.16, EMBID M.28, FERRANT L.8, FERRARI A.5, FERREIRA–MARQUES R.25, FRAIS–KOELBL H.3, FURMAN W.26, FURSOV B.27, GARZON J.A.32, GIOMATARIS I.10, GLEDENOV Y.26, GONZALEZ–ROMERO E.28, GOVERDOVSKI A.27, GRAMEGNA F.19, GRIESMAYER E.3, GUNSING F.10, HAIGHT R.37, HEIL M.11, HOLLANDER P.36, IOANNIDES K.G.15, IOANNOU P.12, ISAEV S.27, JERICHA E.1, KADI Y.5, KAEPPELER F.11, KARADIMOS D.17, KARAMANIS D.15, KAYUKOV A.26, KAZAKOV L.27, KELIC A.9, KETLEROV V.27, KITIS G.16, KOEHLER P.E.38., KOPACH Y.26, KOSSIONIDES E.14, KROSHKINA I.27, LACOSTE V.5, LAMBOUDIS C.16, LEEB H.1, LEPRETRE A.10, LOPES M.25, LOZANO M.31, MARRONE S.20, MARTINEZ-VAL J. -
THE NATURAL RADIOACTIVITY of the BIOSPHERE (Prirodnaya Radioaktivnost' Iosfery)
XA04N2887 INIS-XA-N--259 L.A. Pertsov TRANSLATED FROM RUSSIAN Published for the U.S. Atomic Energy Commission and the National Science Foundation, Washington, D.C. by the Israel Program for Scientific Translations L. A. PERTSOV THE NATURAL RADIOACTIVITY OF THE BIOSPHERE (Prirodnaya Radioaktivnost' iosfery) Atomizdat NMoskva 1964 Translated from Russian Israel Program for Scientific Translations Jerusalem 1967 18 02 AEC-tr- 6714 Published Pursuant to an Agreement with THE U. S. ATOMIC ENERGY COMMISSION and THE NATIONAL SCIENCE FOUNDATION, WASHINGTON, D. C. Copyright (D 1967 Israel Program for scientific Translations Ltd. IPST Cat. No. 1802 Translated and Edited by IPST Staff Printed in Jerusalem by S. Monison Available from the U.S. DEPARTMENT OF COMMERCE Clearinghouse for Federal Scientific and Technical Information Springfield, Va. 22151 VI/ Table of Contents Introduction .1..................... Bibliography ...................................... 5 Chapter 1. GENESIS OF THE NATURAL RADIOACTIVITY OF THE BIOSPHERE ......................... 6 § Some historical problems...................... 6 § 2. Formation of natural radioactive isotopes of the earth ..... 7 §3. Radioactive isotope creation by cosmic radiation. ....... 11 §4. Distribution of radioactive isotopes in the earth ........ 12 § 5. The spread of radioactive isotopes over the earth's surface. ................................. 16 § 6. The cycle of natural radioactive isotopes in the biosphere. ................................ 18 Bibliography ................ .................. 22 Chapter 2. PHYSICAL AND BIOCHEMICAL PROPERTIES OF NATURAL RADIOACTIVE ISOTOPES. ........... 24 § 1. The contribution of individual radioactive isotopes to the total radioactivity of the biosphere. ............... 24 § 2. Properties of radioactive isotopes not belonging to radio- active families . ............ I............ 27 § 3. Properties of radioactive isotopes of the radioactive families. ................................ 38 § 4. Properties of radioactive isotopes of rare-earth elements . -
Uranium Fact Sheet
Fact Sheet Adopted: December 2018 Health Physics Society Specialists in Radiation Safety 1 Uranium What is uranium? Uranium is a naturally occurring metallic element that has been present in the Earth’s crust since formation of the planet. Like many other minerals, uranium was deposited on land by volcanic action, dissolved by rainfall, and in some places, carried into underground formations. In some cases, geochemical conditions resulted in its concentration into “ore bodies.” Uranium is a common element in Earth’s crust (soil, rock) and in seawater and groundwater. Uranium has 92 protons in its nucleus. The isotope2 238U has 146 neutrons, for a total atomic weight of approximately 238, making it the highest atomic weight of any naturally occurring element. It is not the most dense of elements, but its density is almost twice that of lead. Uranium is radioactive and in nature has three primary isotopes with different numbers of neutrons. Natural uranium, 238U, constitutes over 99% of the total mass or weight, with 0.72% 235U, and a very small amount of 234U. An unstable nucleus that emits some form of radiation is defined as radioactive. The emitted radiation is called radioactivity, which in this case is ionizing radiation—meaning it can interact with other atoms to create charged atoms known as ions. Uranium emits alpha particles, which are ejected from the nucleus of the unstable uranium atom. When an atom emits radiation such as alpha or beta particles or photons such as x rays or gamma rays, the material is said to be undergoing radioactive decay (also called radioactive transformation). -
A Note on Radioactive Materials and Their Measurements Elements Are
A NOTE ON RADIOACTIVE MATERIALS AND THEIR MEASUREMENTS Elements are placed in the periodic table of elements according to atomic number or proton number often referred to as Z. Their atomic weights are also usually indicated and can be fractional if the element in nature contains more than one isotope. Isotopes of an element all have the same atomic number, Z, but have different numbers of neu- trons. Some of these isotopes, even in naturally occurring elements, may be radioactive, and are usually given the atomic weight of the longest known isotope. Radioactive decay occurs when an unstable atom loses energy by emitting particles and gamma radiation or by spontaneously fission- ing. (Spontaneous fission is one of the natural modes of radioactive decay in which fission occurs without the addition of external energy or particles.) The activity of a radioactive sample is simply the rate of radioactive decay, expressed as the number of decays per unit time. Traditionally, the curie (Ci) was used to quantify the decay rate and was defined as the radioactivity measured for one gram of pure radium, or ~3.7 × 1010 decays per second (d/s), but the value changed as measurement techniques improved. To avoid this problem of a “chang- ing” constant, the Curie is now defined as exactly 3.7 × 1010 d/s. The becquerel (Bq), equal to one d/s, is the official SI unit (International System of Units). The roentgen R( ) is commonly used as a unit of radiation exposure to X-ray or gamma radiation, and can be roughly defined as “that quan- tity of X-ray or gamma radiation needed to produce one electrostatic unit of ionic charge in one cm3 of air under standard temperature and pressure (STP) “normal conditions”. -
12 Natural Isotopes of Elements Other Than H, C, O
12 NATURAL ISOTOPES OF ELEMENTS OTHER THAN H, C, O In this chapter we are dealing with the less common applications of natural isotopes. Our discussions will be restricted to their origin and isotopic abundances and the main characteristics. Only brief indications are given about possible applications. More details are presented in the other volumes of this series. A few isotopes are mentioned only briefly, as they are of little relevance to water studies. Based on their half-life, the isotopes concerned can be subdivided: 1) stable isotopes of some elements (He, Li, B, N, S, Cl), of which the abundance variations point to certain geochemical and hydrogeological processes, and which can be applied as tracers in the hydrological systems, 2) radioactive isotopes with half-lives exceeding the age of the universe (232Th, 235U, 238U), 3) radioactive isotopes with shorter half-lives, mainly daughter nuclides of the previous catagory of isotopes, 4) radioactive isotopes with shorter half-lives that are of cosmogenic origin, i.e. that are being produced in the atmosphere by interactions of cosmic radiation particles with atmospheric molecules (7Be, 10Be, 26Al, 32Si, 36Cl, 36Ar, 39Ar, 81Kr, 85Kr, 129I) (Lal and Peters, 1967). The isotopes can also be distinguished by their chemical characteristics: 1) the isotopes of noble gases (He, Ar, Kr) play an important role, because of their solubility in water and because of their chemically inert and thus conservative character. Table 12.1 gives the solubility values in water (data from Benson and Krause, 1976); the table also contains the atmospheric concentrations (Andrews, 1992: error in his Eq.4, where Ti/(T1) should read (Ti/T)1); 2) another category consists of the isotopes of elements that are only slightly soluble and have very low concentrations in water under moderate conditions (Be, Al). -
Radionuclides (Including Radon, Radium and Uranium)
Radionuclides (including Radon, Radium and Uranium) Hazard Summary Uranium, radium, and radon are naturally occurring radionuclides found in the environment. No information is available on the acute (short-term) noncancer effects of the radionuclides in humans. Animal studies have reported inflammatory reactions in the nasal passages and kidney damage from acute inhalation exposure to uranium. Chronic (long-term) inhalation exposure to uranium and radon in humans has been linked to respiratory effects, such as chronic lung disease, while radium exposure has resulted in acute leukopenia, anemia, necrosis of the jaw, and other effects. Cancer is the major effect of concern from the radionuclides. Radium, via oral exposure, is known to cause bone, head, and nasal passage tumors in humans, and radon, via inhalation exposure, causes lung cancer in humans. Uranium may cause lung cancer and tumors of the lymphatic and hematopoietic tissues. EPA has not classified uranium, radon or radium for carcinogenicity. Please Note: The main sources of information for this fact sheet are EPA's Integrated Risk Information System (IRIS) (5), which contains information on oral chronic toxicity and the RfD for uranium, and the Agency for Toxic Substances and Disease Registry's (ATSDR's) Toxicological Profiles for Uranium, Radium, and Radon. (1) Uses Uranium is used in nuclear power plants and nuclear weapons. Very small amounts are used in photography for toning, in the leather and wood industries for stains and dyes, and in the silk and wood industries. (2) Radium is used as a radiation source for treating neoplastic diseases, as a radon source, in radiography of metals, and as a neutron source for research. -
1 Introduction
1 Introduction WHO commissions reviews and undertakes health risk assessments associated with exposure to potentially hazardous physical, chemical and biological agents in the home, work place and environment. This monograph on the chemical and radiological hazards associated with exposure to depleted uranium is one such assessment. The purpose of this monograph is to provide generic information on any risks to health from depleted uranium from all avenues of exposure to the body and from any activity where human exposure could likely occur. Such activities include those involved with fabrication and use of DU products in industrial, commercial and military settings. While this monograph is primarily on DU, reference is also made to the health effects and behaviour of uranium, since uranium acts on body organs and tissues in the same way as DU and the results and conclusions from uranium studies are considered to be broadly applicable to DU. However, in the case of effects due to ionizing radiation, DU is less radioactive than uranium. This review is structured as broadly indicated in Figure 1.1, with individual chapters focussing on the identification of environmental and man-made sources of uranium and DU, exposure pathways and scenarios, likely chemical and radiological hazards and where data is available commenting on exposure-response relationships. HAZARD IDENTIFICATION PROPERTIES PHYSICAL CHEMICAL BIOLOGICAL DOSE RESPONSE RISK EVALUATION CHARACTERISATION BACKGROUND EXPOSURE LEVELS EXPOSURE ASSESSMENT Figure 1.1 Schematic diagram, depicting areas covered by this monograph. It is expected that the monograph could be used as a reference for health risk assessments in any application where DU is used and human exposure or contact could result. -
Highly Enriched Uranium: Striking a Balance
OFFICIAL USE ONLY - DRAFT GLOSSARY OF TERMS APPENDIX F GLOSSARY OF TERMS Accountability: That part of the safeguards and security program that encompasses the measurement and inventory verification systems, records, and reports to account for nuclear materials. Assay: Measurement that establishes the total quantity of the isotope of an element and the total quantity of that element. Atom: The basic component of all matter. Atoms are the smallest part of an element that have all of the chemical properties of that element. Atoms consist of a nucleus of protons and neutrons surrounded by electrons. Atomic energy: All forms of energy released in the course of nuclear fission or nuclear transformation. Atomic weapon: Any device utilizing atomic energy, exclusive of the means for transportation or propelling the device (where such means is a separable and divisible part of the device), the principal purpose of which is for use as, or for development of, a weapon, a weapon prototype, or a weapon test device. Blending: The intentional mixing of two different assays of the same material in order to achieve a desired third assay. Book inventory: The quantity of nuclear material present at a given time as reflected by accounting records. Burnup: A measure of consumption of fissionable material in reactor fuel. Burnup can be expressed as (a) the percentage of fissionable atoms that have undergone fission or capture, or (b) the amount of energy produced per unit weight of fuel in the reactor. Chain reaction: A self-sustaining series of nuclear fission reactions. Neutrons produced by fission cause more fission. Chain reactions are essential to the functioning of nuclear reactors and weapons. -
A Global Scavenging and Circulation Ocean Model of Thorium-230 and Protactinium-231 with Improved Particle Dynamics (NEMO–Prothorp 0.1)
Geosci. Model Dev., 11, 3537–3556, 2018 https://doi.org/10.5194/gmd-11-3537-2018 © Author(s) 2018. This work is distributed under the Creative Commons Attribution 4.0 License. A global scavenging and circulation ocean model of thorium-230 and protactinium-231 with improved particle dynamics (NEMO–ProThorP 0.1) Marco van Hulten1,2, Jean-Claude Dutay1, and Matthieu Roy-Barman1 1Laboratoire des Sciences du Climat et de l’Environnement, IPSL, CEA–Orme des Merisiers, 91191 Gif-sur-Yvette, France 2Geophysical Institute, University of Bergen, Bergen, Norway Correspondence: Marco van Hulten ([email protected]) Received: 1 November 2017 – Discussion started: 8 December 2017 Revised: 16 August 2018 – Accepted: 20 August 2018 – Published: 31 August 2018 Abstract. In this paper we set forth a 3-D ocean model of the can be done based on our model as its source code is readily radioactive trace isotopes 230Th and 231Pa. The interest arises available. from the fact that these isotopes are extensively used for in- vestigating particle transport in the ocean and reconstructing past ocean circulation. The tracers are reversibly scavenged 1 Introduction by biogenic and lithogenic particles. Our simulations of 230Th and 231Pa are based on the Oceanic circulation and the carbon cycle play a major role NEMO–PISCES ocean biogeochemistry general circulation in the regulation of the past and present climate. Heat and model, which includes biogenic particles, namely small and carbon dioxide in the atmosphere tend to equilibrate with the big particulate organic carbon, calcium carbonate and bio- ocean surface and are transported down into the deep ocean genic silica. -
Use of Isotopic Signature of Radionuclides Released from Uranium Mines and Mills to Discriminate Low Levels of Environmental Impact Against Natural Background Levels
XA9745957 USE OF ISOTOPIC SIGNATURE OF RADIONUCLIDES RELEASED FROM URANIUM MINES AND MILLS TO DISCRIMINATE LOW LEVELS OF ENVIRONMENTAL IMPACT AGAINST NATURAL BACKGROUND LEVELS P. ZETTWOOG, N. LEMAITRE Office de protection contre les rayonnements Ionisants, Le Vesinet S. BERNHARD, Y. VAUZELLE ALGADE, Bessines sur Gartempe France Abstract In France, uranium ores have been exploited in rural areas with a low population density. The critical population group which is identified for radiological impact studies lives close to the uranium facilities, at distances from a few hundred metres to 1 kilometre. Within this range, the radioactivity of the environment is still detectable amongst the natural background. Mining companies manage surveillance networks according to strict specifications laid down by the government authorities. For active mining operations it is the exposure to daughter products of radon 222 that forms the bulk of the total effective dose. After closure of a mine and rehabilitation of the site, products such as uranium 238 and radium 226 in the water can become the major components of the total effective dose. Surveillance networks are built to allow direct measurement of the radon daughter products critical to the alpha energy and measurements of the water activities for uranium 238 and radium 226. Annual limits for the effective individual doses are given and determined by the authorities. The industry must manage effective annual doses of the order of 1 mSv. The natural exposure which is not part of the regulation is of the same order (1 mSv) as the exposure created by the industry. The results given are therefore lacking in clarity for the public. -
Uranium (U) Fact Sheet
Uranium (U) September 2003 Fact Sheet 320-079 Division of Environmental Health Office of Radiation Protection WHO DISCOVERED URANIUM? Uranium was discovered by Martin Klaproth, a German chemist, in 1789 in the mineral pitchblende, and was named after the planet Uranus. Some of the important isotopes of uranium are: ♦ U235 (half-life 703,800,000 years) ♦ U238 (half-life 4,468,000,000 years) WHAT IS URANIUM USED FOR? In the past, uranium was used to color glass (from as early as 79 AD) and deposits were once mined in order to obtain its decay product, radium. This element was used in luminous paint, particularly on the dials of watches and aircraft instruments, and in medicine for the treatment of disease. Uranium was popular as an orange coloring agent for ceramic glazes on Fiesta Ware until its use was restricted in 1943, and as an additive in porcelain teeth to improve their appearance. Until the 1970s, virtually all of the uranium that was mined was used in the production of nuclear weapons. Today the only substantial use for uranium is as fuel in nuclear reactors, mostly in nuclear power plants for electricity generation. Uranium-235 is the only naturally occurring material which can sustain a fission chain reaction, releasing large amounts of energy. Uranium Fuel Natural uranium is composed of 0.72% U-235 (the fissionable isotope), 99.27% U-238, and a trace quantity 0.0055% U-234. The 0.72% U-235 is not sufficient to produce a self-sustaining critical chain reaction in U.S. style light-water reactors, although it is used in Canadian CANDU reactors. -
Periodic Table of Elements
The origin of the elements – Dr. Ille C. Gebeshuber, www.ille.com – Vienna, March 2007 The origin of the elements Univ.-Ass. Dipl.-Ing. Dr. techn. Ille C. Gebeshuber Institut für Allgemeine Physik Technische Universität Wien Wiedner Hauptstrasse 8-10/134 1040 Wien Tel. +43 1 58801 13436 FAX: +43 1 58801 13499 Internet: http://www.ille.com/ © 2007 © Photographs of the elements: Mag. Jürgen Bauer, http://www.smart-elements.com 1 The origin of the elements – Dr. Ille C. Gebeshuber, www.ille.com – Vienna, March 2007 I. The Periodic table............................................................................................................... 5 Arrangement........................................................................................................................... 5 Periodicity of chemical properties.......................................................................................... 6 Groups and periods............................................................................................................. 6 Periodic trends of groups.................................................................................................... 6 Periodic trends of periods................................................................................................... 7 Examples ................................................................................................................................ 7 Noble gases .......................................................................................................................