2007: 3Rd Quarter
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The Effect of Chemical Incidents on First Responders
2019 The Effect of Chemical Incidents on First Responders: An Interview with Bruce Evans (MPA, NRP, CFOD, SEMSO), Fire Chief, Upper Pine River Fire Protection District A massive leak of liquefied chlorine gas created a dangerous cloud over the city of Henderson, NV, in the early morning hours of May 6, 1991. Over 200 people (including firefighters) were examined at a local hospital for respiratory distress caused by inhalation of the chlorine and approximately 30 were admitted for treatment. Approximately 700 individuals were taken to shelters, and between 2,000 and 7,000 individuals were evacuated from the area. ASPR TRACIE interviewed Chief Bruce Evans (who was a firefighter- paramedic at the time of the incident), asking him to share his my first large-scale incident: the experiences and highlight how the PEPCON explosion. PEPCON was Access these U.S. Fire Administration Technical Reports fire and emergency response to a rocket fuel plant that supplied propellant used for the space for more information on these chemical incidents has changed incidents: over the years. shuttle program. This explosion sent a shock wave over the • Fire and Explosions at Rocket Corina Solé Brito, ASPR TRACIE entire Las Vegas Valley, blew out Fuel Plant (CSB): Can you please share windows that were miles away, • Massive Leak of Liquefied your experience in Henderson and created a small, multicolored Chlorine Gas and other related incidents, how mushroom cloud on the south end you think the field has changed of the valley. The Professional since then, and what you think Golfers’ Association (PGA) was the future holds? also in town, so there were satellite or injuries from flying debris were I am fortunate trucks and news trucks present. -
Advanced Nuclear Power and Fuel Cycle Technologies: Outlook and Policy Options
Order Code RL34579 Advanced Nuclear Power and Fuel Cycle Technologies: Outlook and Policy Options July 11, 2008 Mark Holt Specialist in Energy Policy Resources, Science, and Industry Division Advanced Nuclear Power and Fuel Cycle Technologies: Outlook and Policy Options Summary Current U.S. nuclear energy policy focuses on the near-term construction of improved versions of existing nuclear power plants. All of today’s U.S. nuclear plants are light water reactors (LWRs), which are cooled by ordinary water. Under current policy, the highly radioactive spent nuclear fuel from LWRs is to be permanently disposed of in a deep underground repository. The Bush Administration is also promoting an aggressive U.S. effort to move beyond LWR technology into advanced reactors and fuel cycles. Specifically, the Global Nuclear Energy Partnership (GNEP), under the Department of Energy (DOE) is developing advanced reprocessing (or recycling) technologies to extract plutonium and uranium from spent nuclear fuel, as well as an advanced reactor that could fully destroy long-lived radioactive isotopes. DOE’s Generation IV Nuclear Energy Systems Initiative is developing other advanced reactor technologies that could be safer than LWRs and produce high-temperature heat to make hydrogen. DOE’s advanced nuclear technology programs date back to the early years of the Atomic Energy Commission in the 1940s and 1950s. In particular, it was widely believed that breeder reactors — designed to produce maximum amounts of plutonium from natural uranium — would be necessary for providing sufficient fuel for a large commercial nuclear power industry. Early research was also conducted on a wide variety of other power reactor concepts, some of which are still under active consideration. -
MOX Fuel Program: Current Plans and Controversy
MOX Fuel Program: Current Plans and Controversy The Mixed Oxide (MOX) Fuel Fabrication Facility at Savannah River, South Carolina is intended to manufacture nuclear fuel from surplus weapons-grade plutonium for use in commercial nuclear energy reactors. However, the project has faced serious delays and massive cost overruns – and currently has no customers for its proposed fuel. As a result, the President’s FY17 Budget Proposal requests $270 million to begin closing the project, while diluting the plutonium for transfer to the Waste Isolation Pilot Plant (WIPP) in New Mexico, a more cost-efficient option. What Is It? The MOX facility at Savannah River was designed to repurpose 3.5 tonnes of surplus weapons-grade plutonium yearly. This facility was intended to play a key role in the United States’ fulfillment of the 2000 Plutonium Management and Disposition Agreement (PMDA) between Russia and the U.S., which affirms each country’s commitment to dispose of 34 metric tonnes of plutonium, enough collectively for 17,000 nuclear weapons. Challenges: The MOX Fuel Fabrication Facility’s anticipated date of operation was 2007, with plutonium disposition set to end in 2020. Multiple delays in construction led to significant cost overruns, with beginning operations delayed until 2019. Initially valued at $2.898 billion (2016 dollars), the total cost of the project skyrocketed to $15.683 billion as a result of construction delays and program mismanagement. This estimate, however, assumes a steady rate of funding, and fluctuations in funding levels could exacerbate delays and cost overruns. Even if completed, the site currently boasts zero customers for MOX fuel. -
Fallout Model for the Robust Nuclear Earth Penetrator Blake Purnell the Radioactive Cloud Model
Fallout Model for the Robust Nuclear Earth Penetrator Blake Purnell Modeling radioactive fallout from nuclear explosions requires a description of the radioactive cloud and base surge and an atmospheric transport model for the cloud dispersion. The atmospheric transport model is independent of the radioactive nature of the dust and I will stick to a simple model in this study. The Radioactive Cloud Model Radioactive Release The first stage in understanding the fallout from a nuclear explosion is to estimate the amount of radioactivity released into the atmosphere. For external exposure to radiation, the main threat is from gamma-rays. The average gamma-ray activity1 produced in a nuclear explosion has been calculated as 530 megacuries per kiloton of fission yield at one hour after the explosion, with an average photon energy of 0.7 MeV. The data available on underground nuclear tests focuses on the fraction of the total activity found in “early” or “close-in” fallout ( Fc ), which measures only those particles that have been deposited in the first 24 2 hours . The fraction of the total activity released into the atmosphere ( f rel ) is greater than what appears in 3 the early fallout ( f rel > Fc ). The fraction Fc is dependant on the scaled depth of burst . A summary of the activity release data available for U.S. and Soviet underground tests are shown in Tables 1, Table 2, and Figure 1. Table 1: Activity Released from U.S. Underground Nuclear Tests. Test Yield Depth of Burst Scaled Depth of Burst Fraction of Total Activity 1/3 (kt) (m) (m/kt ) in Early Fallout (Fc) Jangle Sa 1.2 0 0 0.50 Jangle Ua 1.2 5.18 4.88 0.64 Teapot ESSa 1.2 20.4 19.2 0.46 Schoonerb 30 111 35.8 0.48 Cabrioletb 2.3 51.8 39.3 0.028 Buggyb,c 1.08 41.1 40.1 0.038 Sedanb,d 100 194 41.7 0.18 Danny Boya 0.43 33.5 44.4 0.04 Sulkyb 0.088 27.4 61.6 0.001 Neptunea 0.115 30.5 62.7 0.005 Blancaa 19 255 95.4 0.0005 a) Release fraction from Knox-65, Table 1. -
In the Shadow of the Mushroom Cloud: Nuclear Testing, Radioactive Fallout and Damage to U.S. Agriculture
In the Shadow of the Mushroom Cloud: Nuclear Testing, Radioactive Fallout and Damage to U.S. Agriculture September 1, 2017 Abstract In the 1950s the United States conducted scores of nuclear tests at the Nevada Test Site (NTS). Each test created tremendous quantities of harmful radioactive material and much of this material deposited across the country with precipitation. This paper is the first in the economics literature to measure some of the external costs of NTS activities. I find that fallout from nuclear tests adversely affected U.S. agriculture for large areas of the country. These empirical results show that nuclear testing had much broader economic and environmental impact than previously thought. The Cold War saw the rapid development and deployment of nuclear weapons. To expedite its nuclear weapons program, the United States started to conduct atmospheric nuclear tests at the Nevada Test Site (NTS) in 1951. This deliberate policy decision created immense quantities of radioactive debris and much of this material rained down across the U.S.. One estimate places the total atmospheric release of radioactive material from the NTS from 1951 to 1963 at 12 billion Curies. In comparison, the partial nuclear meltdown at Chernobyl released approximately 81 million Curies of radioactive material (LeBaron, 1998). Knowledge regarding the impact of this pollution is limited to scientific and health studies conducted in the regions surrounding the NTS. Nuclear testing had large pollution externalities associated with it, but the magnitude and extent of the nationwide harm caused by NTS activities have yet to be measured. This paper quantifies one dimension of the external costs of these activities by studying the adverse effects of radioactive fallout on U.S. -
Management of Reprocessed Uranium Current Status and Future Prospects
IAEA-TECDOC-1529 Management of Reprocessed Uranium Current Status and Future Prospects February 2007 IAEA-TECDOC-1529 Management of Reprocessed Uranium Current Status and Future Prospects February 2007 The originating Section of this publication in the IAEA was: Nuclear Fuel Cycle and Materials Section International Atomic Energy Agency Wagramer Strasse 5 P.O. Box 100 A-1400 Vienna, Austria MANAGEMENT OF REPROCESSED URANIUM IAEA, VIENNA, 2007 IAEA-TECDOC-1529 ISBN 92–0–114506–3 ISSN 1011–4289 © IAEA, 2007 Printed by the IAEA in Austria February 2007 FOREWORD The International Atomic Energy Agency is giving continuous attention to the collection, analysis and exchange of information on issues of back-end of the nuclear fuel cycle, an important part of the nuclear fuel cycle. Reprocessing of spent fuel arising from nuclear power production is one of the strategies for the back end of the fuel cycle. As a major fraction of spent fuel is made up of uranium, chemical reprocessing of spent fuel would leave behind large quantities of separated uranium which is designated as reprocessed uranium (RepU). Reprocessing of spent fuel could form a crucial part of future fuel cycle methodologies, which currently aim to separate and recover plutonium and minor actinides. The use of reprocessed uranium (RepU) and plutonium reduces the overall environmental impact of the entire fuel cycle. Environmental considerations will be important in determining the future growth of nuclear energy. It should be emphasized that the recycling of fissile materials not only reduces the toxicity and volumes of waste from the back end of the fuel cycle; it also reduces requirements for fresh milling and mill tailings. -
Appendix B Differences Between Thermal and Radiation Properties of Mixed Oxide and Low-Enriched Uranium Radioactive Materials
APPENDIX B DIFFERENCES BETWEEN THERMAL AND RADIATION PROPERTIES OF MIXED OXIDE AND LOW-ENRICHED URANIUM RADIOACTIVE MATERIALS The contents considered in this Standard Review Plan (SRP) appendix are unirradiated mixed oxide (MOX) radioactive material (RAM), in the form of powder, pellets, fresh fuel rods, or fresh reactor fuel assemblies. Unirradiated MOX RAM will also be referred to in this appendix as MOX fresh fuel. This appendix summarizes the relative degree of differences between the thermal and radiation properties of the various MOX RAM contents relative to similar properties for analogous low-enriched uranium (LEU) RAM contents. MOX fresh fuel can be made with plutonium having various compositions of plutonium isotopes. The discussion in this appendix makes use of the 3013 Standard (DOE 2012), which specifies the typical grades of plutonium that are used to make the MOX fresh fuel. The actual plutonium compositions found in practice may not match these compositions exactly, but these grades can be considered typical for the purposes of this appendix. Table B–6 of the 3013 Standard gives weight percents for various plutonium isotopes in various grades of plutonium. They are reproduced in the following table (Table B–1) as representative values for typical grades of plutonium that might be used to fabricate MOX fresh fuel. Pure plutonium-239 has been included to contrast the effect of the other plutonium isotopes. Note that in addition to the isotopes identified in Table B–1, plutonium will contain plutonium-236 and americium-241 (from plutonium-241 decay). Initially, it is expected that MOX fresh fuel will be fabricated using weapons grade (WG) plutonium. -
Framatome ANP MOX Fuel Design
BAW-10238(NP) Revision 0 43-10238NP-00 MOX Fuel Design Report March 2002 Framatome ANP, Inc. U.S. Nuclear Regulatory Commission Report Disclaimer Important Notice Regarding the Contents and Use of This Document Please Read Carefully This technical report was derived through research and development programs sponsored by Framatome ANP, Inc. It is being submitted by Framatome ANP, Inc. to the U.S. Nuclear Regulatory Commission as part of a technical contribution to facilitate safety analyses by licensees of the U.S. Nuclear Regulatory Commission which utilize Framatome ANP, Inc. fabricated reload fuel or technical services provided by Framatome ANP, Inc. for light water power reactors and it is true and correct to the best of Framatome ANP, Inc.'s knowledge, information, and belief. The information contained herein may be used by the U.S. Nuclear Regulatory Commission in its review of this report and, under the terms of the respective agreements, by licensees or applicants before the U.S. Nuclear Regulatory Commission which are customers of Framatome ANP, Inc. in their demonstration of compliance with the U.S. Nuclear Regulatory Commission's regulations. Framatome ANP, Inc.'s warranties and representations concerning the subject matter of this document are those set forth in the agreement between Framatome ANP, Inc. and the Customer pursuant to which this document is issued. Accordingly, except as otherwise expressly provided in such agreement, neither Framatome ANP, Inc. nor any person acting on its behalf: a. makes any warranty, or representation, express or implied, with respect to the accuracy, completeness, or usefulness of the information contained in this document, or that the use of any information, apparatus, method, or process disclosed in this document will not infringe privately owned rights; or b. -
A Review of the Nuclear Fuel Cycle Strategies and the Spent Nuclear Fuel Management Technologies
energies Review A Review of the Nuclear Fuel Cycle Strategies and the Spent Nuclear Fuel Management Technologies Laura Rodríguez-Penalonga * ID and B. Yolanda Moratilla Soria ID Cátedra Rafael Mariño de Nuevas Tecnologías Energéticas, Universidad Pontificia Comillas, 28015 Madrid, Spain; [email protected] * Correspondence: [email protected]; Tel.: +34-91-542-2800 (ext. 2481) Received: 19 June 2017; Accepted: 6 August 2017; Published: 21 August 2017 Abstract: Nuclear power has been questioned almost since its beginnings and one of the major issues concerning its social acceptability around the world is nuclear waste management. In recent years, these issues have led to a rise in public opposition in some countries and, thus, nuclear energy has been facing even more challenges. However, continuous efforts in R&D (research and development) are resulting in new spent nuclear fuel (SNF) management technologies that might be the pathway towards helping the environment and the sustainability of nuclear energy. Thus, reprocessing and recycling of SNF could be one of the key points to improve the social acceptability of nuclear energy. Therefore, the purpose of this paper is to review the state of the nuclear waste management technologies, its evolution through time and the future advanced techniques that are currently under research, in order to obtain a global vision of the nuclear fuel cycle strategies available, their advantages and disadvantages, and their expected evolution in the future. Keywords: nuclear energy; nuclear waste management; reprocessing; recycling 1. Introduction Nuclear energy is a mature technology that has been developing and improving since its beginnings in the 1940s. However, the fear of nuclear power has always existed and, for the last two decades, there has been a general discussion around the world about the future of nuclear power [1,2]. -
Oxygen Isotope Composition of Trinitite Postdetonation Materials Elizabeth C
Article pubs.acs.org/ac Oxygen Isotope Composition of Trinitite Postdetonation Materials Elizabeth C. Koeman,* Antonio Simonetti, Wei Chen, and Peter C. Burns Department of Civil Engineering and Environment Engineering and Earth Sciences, University of Notre Dame, Notre Dame, Indiana 46556, United States *S Supporting Information ABSTRACT: Trinitite is the melt glass produced subsequent the first nuclear bomb test conducted on July 16, 1945, at White Sands Range (Alamagordo, NM). The geological background of the latter consists of arkosic sand that was fused with radioactive debris and anthropogenic materials at ground zero subsequent detonation of the device. Postdetonation materials from historic nuclear weapon test sites provide ideal samples for development of novel forensic methods for attribution and studying the chemical/isotopic effects of the explosion on the natural geological environment. In particular, the latter effects can be evaluated relative to their spatial distribution from ground zero. We report here δ18O(‰) values for nonmelted, precursor minerals phases (quartz, feldspar, calcite), “feldspathic-rich” glass, “average” melt glass, and bulk (natural) unmelted sand from the Trinity site. Prior to oxygen isotope analysis, grains/crystals were examined using scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS) to determine their corresponding major element composition. δ18O values for bulk trinitite samples exhibit a large range (11.2−15.5‰) and do not correlate with activity levels for activation product 152Eu; the latter levels are a function of their spatial distribution relative to ground zero. Therefore, the slow neutron flux associated with the nuclear explosion did not perturb the 18O/16O isotope systematics. The oxygen isotope values do correlate with the abundances of major elements derived from precursor minerals present within the arkosic sand. -
The Uncertain Consequences of Nuclear Weapons Use
THE UNCERTAIN CONSEQUENCES OF NUCLEAR WEAPONS USE Michael J. Frankel James Scouras George W. Ullrich Copyright © 2015 The Johns Hopkins University Applied Physics Laboratory LLC. All Rights Reserved. NSAD-R-15-020 THE UNCERTAIN CONSEQUENCES OF NUCLEAR WEAPONS USE iii Contents Figures ................................................................................................................................................................................................ v Abstract ............................................................................................................................................................................................vii Overview ....................................................................................................................................................................1 Historical Context .....................................................................................................................................................2 Surprises ..................................................................................................................................................................................... 4 Enduring Uncertainties, Waning Resources ................................................................................................................10 Physical Effects: What We Know, What Is Uncertain, and Tools of the Trade .............................................. 12 Nuclear Weapons Effects Phenomena...........................................................................................................................13 -
ATOM for PEACE, NOT for WAR Prof
AUGUST, 2014 ATOM FOR PEACE, NOT FOR WAR Prof. Manashi Goswami ComeAugust,thewhole worldremembers Three otherplanes had left earlierin orderto two frightfuldays ofworld history,August 6th ascertain the weather condition over the and 9th, 1945. The atomic bombings of the possibletargets.On thehookinthe ceiling of cities of Hiroshima and Nagasaki in Japan the plane hung the ten- foot atomic bomb wereconducted onthesedays by theUnited "Little Boy". On 6th August,1945, the first States during the finalstageofWorld WarII. choice target Hiroshima, was having clear These two bombings werethefirst and remain weather.At 8:15(am) localtime, Enola Gay's theonly useofnuclearweapons in warfare. doorsprangopen and itdroppedthe little boy. By August1945, theallied Manhattan project had successfully tested an atomic deviceand had produced weapons based on two alternate designs.Auranium gun type atomic bomb (Little Boy) was dropped on Hiroshima on August 6,1945, followed by a Plutoniumimplosion-type bomb (Fat Man) onthecity ofNagasakionAugust 9. Within thefirsttwo to fourmonths of thebombing, The Mushroom Cloud acute effect killed 90,000 - 166,000 people Thebomb exploded 1,900feet abovethe in Hiroshima and 60,000 - 80,000 in city.The mushroom cloud itself was a Nagasaki. During the following months large number of people died various radiation spectacularsight.Abubbling mass ofpurple- effects and injuries. gray smoke with a hot red burning core estimated to have reached a height of 40,000 On the Day feet.Such was the description of dreadful At 2.45 amonMonday,August 6,1945a devastation that tookplaceon6th August1945 B-29 bomber plane,the Enola Gay tookoff at Hiroshima city. from Tinian, a north pacific island in the Why Hiroshima Marinianas,1500 miles south of Japan.