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Dead Time and Count Loss Determination for Radiation Detection Systems in High Count Rate Applications
Scholars' Mine Doctoral Dissertations Student Theses and Dissertations Spring 2010 Dead time and count loss determination for radiation detection systems in high count rate applications Amol Patil Follow this and additional works at: https://scholarsmine.mst.edu/doctoral_dissertations Part of the Nuclear Engineering Commons Department: Nuclear Engineering and Radiation Science Recommended Citation Patil, Amol, "Dead time and count loss determination for radiation detection systems in high count rate applications" (2010). Doctoral Dissertations. 2148. https://scholarsmine.mst.edu/doctoral_dissertations/2148 This thesis is brought to you by Scholars' Mine, a service of the Missouri S&T Library and Learning Resources. This work is protected by U. S. Copyright Law. Unauthorized use including reproduction for redistribution requires the permission of the copyright holder. For more information, please contact [email protected]. DEAD TIME AND COUNT LOSS DETERMINATION FOR RADIATION DETECTION SYSTEMS IN HIGH COUNT RATE APPLICATIONS by AMOL PATIL A DISSERTATION Presented to the Faculty of the Graduate School of the MISSOURI UNIVERSITY OF SCIENCE AND TECHNOLOGY In Partial Fulfillment of the Requirements for the Degree DOCTOR OF PHILOSOPHY in NUCLEAR ENGINEERING 2010 Approved by Shoaib Usman, Advisor Arvind Kumar Gary E. Mueller Carlos H. Castano Bijaya J. Shrestha © 2010 AMOL PATIL All Rights Reserved iii PUBLICATION DISSERTATION OPTION This dissertation consists of the following two articles that have been, or will be submitted for publication as follows: Pages 4-40 are intended for submission to Journal of Radioanalytical and Nuclear Chemistry. Pages 41-62 have been published in Nuclear Technologies journal (February, 2009). iv ABSTRACT This research is focused on dead time and the subsequent count loss estimation in radiation detection systems. -
Concurrent Reduction and Distillation; an Improved Technique for the Recovery and Chemical Refinement of the Isotopes of Cadmium and Zinc*
If I CONCURRENT REDUCTION AND DISTILLATION; AN IMPROVED TECHNIQUE FOR THE RECOVERY AND CHEMICAL REFINEMENT OF THE ISOTOPES OF CADMIUM AND ZINC* H. H. Cardill L. E. McBride LOHF-821046—2 E. W. McDaniel DE83 001931 Operations Division Oak Ridge National Laboratory Oak Ridge, Tennessee 3 7830 .DISCLAIMER • s prepared es an accouni oi WOTk sconsQ'ed by an agency of itie United Slates Cover r "iiit?3 Stilt 65 Gov(?fnft»gn ^ ri(jt ^nv aQcncy Tllf GO* ^or rlny O^ tt^^ir ^rnployut^. TigV MASTER lostifl. ion, apod'aiuj pioiJut;. <y vned nghtv Reference hcein xc any v>t^-'T*t. ^ Dv ^.r^de narno, tf^Oernafk^ mir'ij'iJClureT. or otrierw «d <Jo*^ •nenaalion. or liivONng bv 'Vhe United _^_ . vs and opinions of authors enp'«i«] herein do noi IOM t' irip UnitK* Stales Govefnrneni c a^v agency For presentation at the 11th World Conference of the International Nuclear Target Development Society, October 6-8, 1982, Seattle, Washington. By acceptance of this article, the publisher or recipient acknowledge* the U.S. Govarnment's right to retain a nonaxclusiva, royalty-frtta license in and to any copyright covering tha article. NOTICE P0T09_0£-Jfns,J^SPQRT_JfgE_Il,LESIBLE. I has been reproauce.1 from the best available aopy to pensit the broadest possible avail- ability* *Research sponsored by the Office of Basic Energy Science, U.S. Department of Energy under contract W-7405-eng-26 with the Union Carbide Co rpcration,, DISTRIBUTION OF THIS DOCUMEHT 18 UNLIMITED ' CONCURRENT REDUCTION AND DISTILLATION - AY. IMPROVED TECHNIQUE FOR THE RECOVERY AND CHEMICAL REFINEMENT OF THE ISOTOPES OF CADMIUM AND ZINC H. -
Optimization of a Gas Flow Proportional Counter for Alpha Decay
Optimization of a gas flow proportional counter for alpha decay measurements Elena Ceballos Romero Master Thesis Institut f¨urKernphysik Mathematisch-Naturwissenschaftliche Fakult¨at Westf¨alische Wilhelms-Universit¨atM¨unster Prof. Dr. Alfons Khoukaz October 2012 III I am among those who think that science has great beauty. A scientist in his laboratory is not only a technician: he is also a child placed before natural phenomena which impress him like a fairy tale. We should not allow it to be believed that all scientific progress can be reduced to mechanisms, machines, gearings, even though such machinery has its own beauty. -Marie Curie A magdalena, por ponerme en este camino. A mis padres, por siempre acompa~narmeen ´el. IV V I certify that I have independently written this thesis and no other sources than the mentioned ones have been used. Referent: Prof. Dr. Alfons Khoukaz Correferent: Dr. Mar´ıaVilla Alfageme VI Contents 1. Introduction 1 2. Introduction to natural radiations 5 2.1. Radioactivity . .5 2.1.1. Decay laws . .5 2.1.2. Activity . .7 2.2. Decays . .7 2.2.1. Alpha decay . .7 2.2.2. Beta decay . .9 2.2.3. Gamma decay . 11 3. Theoretical background: Gas-filled detectors 13 3.1. General properties . 13 3.1.1. Number of ion pairs formed . 14 3.1.2. Behaviour of charged particles in gases . 14 3.1.3. Operational modes of gas detectors . 15 3.2. Proportional counters: gas multiplication effect . 17 3.3. Gas flow detectors . 18 4. Experimental set-up 21 4.1. Detector . 21 4.1.1. -
KULAGE-DISSERTATION-2013.Pdf
ENCRYPTED NANOPARTICLES FOR SECURITY, COUNTER-INDUSTRIAL ESPIONAGE, AND COUNTERFEITING A Dissertation by ZACHARY ANDREW KULAGE Submitted to the Office of Graduate and Professional Studies of Texas A&M University in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY Chair of Committee, William S. Charlton Committee Members, Sean M. McDeavitt John W. Poston, Sr. Charles M. Folden III Head of Department, Yassin A. Hassan December 2013 Major Subject: Nuclear Engineering Copyright 2013 Zachary Andrew Kulage ABSTRACT Acts of terrorism and the use of explosives raise concerns about what can be done to prevent such acts. From stopping such a threat to preventing the illicit counterfeiting and smuggling of sensitive and proprietary goods, identification tag- gant technology can be applied to identify and interdict materials of a dubious na- ture. This cost effective approach to tag and track materials will find application in both the government and private sectors, particularly in the prevention of corporate espionage. A taggant system was created based on the modification of the natural isotopic vector of cadmium and tellurium to create artificial, unique, and robust identification capabilities. A proof of concept trial was undertaken to ascertain the effectiveness, reliability, and integrity of a system. Stable isotopes were mixed in various combi- nations to alter the isotopic vector and then neutron activation analysis techniques were used to evaluate the quality of the taggants. Two different neutron activation analysis facilities of differing capabilities were employed to test the limitations of the method in detection of trace amounts of taggant material. Testing of the taggant system found that solid phase taggants were capable of producing around 14,000 unique taggants for under $250 each while liquid phase taggants were capable of producing around 2,000 unique taggants for under $50 each. -
Neutron Capture Cross Sections of Cadmium Isotopes
Neutron Capture Cross Sections of Cadmium Isotopes By Allison Gicking A thesis submitted to Oregon State University In partial fulfillment of the requirements for the degree of Bachelor of Science Presented June 8, 2011 Commencement June 17, 2012 Abstract The neutron capture cross sections of 106Cd, 108Cd, 110Cd, 112Cd, 114Cd and 116Cd were determined in the present project. Four different OSU TRIGA reactor facilities were used to produce redundancy in the results and to measure the thermal cross section and resonance integral separately. When the present values were compared with previously measured values, the differences were mostly due to the kind of detector used or whether or not the samples were natural cadmium. Some of the isotopes did not have any previously measured values, and in that case, new information about the cross sections of those cadmium isotopes has been provided. Table of Contents I. Introduction………………………………………………………………….…….…1 II. Theory………………………………………………………………………...…...…3 1. Neutron Capture…………………………………………………….….……3 2. Resonance Integral vs. Effective Thermal Cross Section…………...………5 3. Derivation of the Activity Equations…………………………………....…..8 III. Methods………………………………………………………….................…...…...12 1. Irradiation of the Samples………………………………………….….....…12 2. Sample Preparation and Parameters………………..………...………..……16 3. Efficiency Calibration of Detectors…………………………..………....…..18 4. Data Analysis…………………………………...…….………………...…..19 5. Absorption by 113Cd……………………………………...……...….………20 IV. Results………………………………………………….……………..……….…….22 -
Arxiv:1305.1738V1 [Nucl-Ex] 8 May 2013 Ae Pcrsoystpa SLECR.High-Energy ISOLDE-CERN
Spins, Electromagnetic Moments, and Isomers of 107-129Cd D. T. Yordanov,1,2, ∗ D. L. Balabanski,3 J. Biero´n,4 M. L. Bissell,5 K. Blaum,1 I. Budinˇcevi´c,5 S. Fritzsche,6 N. Fr¨ommgen,7 G. Georgiev,8 Ch. Geppert,6, 7 M. Hammen,7 M. Kowalska,2 K. Kreim,1 A. Krieger,7 R. Neugart,7 W. N¨ortersh¨auser,6, 7 J. Papuga,5 and S. Schmidt6 1Max-Planck-Institut f¨ur Kernphysik, Saupfercheckweg 1, D-69117 Heidelberg, Germany 2CERN European Organization for Nuclear Research, Physics Department, CH-1211 Geneva 23, Switzerland 3INRNE, Bulgarian Academy of Science, BG-1784 Sofia, Bulgaria 4Instytut Fizyki imienia Mariana Smoluchowskiego, Uniwersytet Jagiello´nski, Reymonta 4, 30-059 Krak´ow, Poland 5Instituut voor Kern- en Stralingsfysica, KU Leuven, Celestijnenlaan 200D, B-3001 Leuven, Belgium 6GSI Helmholtzzentrum f¨ur Schwerionenforschung GmbH, D-64291 Darmstadt, Germany 7Institut f¨ur Kernchemie, Johannes Gutenberg-Universit¨at Mainz, D-55128 Mainz, Germany 8CSNSM-IN2P3-CNRS, Universit´ede Paris Sud, F-91405 Orsay, France (Dated: October 7, 2018) The neutron-rich isotopes of cadmium up to the N = 82 shell closure have been investigated by high-resolution laser spectroscopy. Deep-UV excitation at 214.5 nm and radioactive-beam bunching provided the required experimental sensitivity. Long-lived isomers are observed in 127Cd and 129Cd for the first time. One essential feature of the spherical shell model is unambiguously confirmed by − a linear increase of the 11/2 quadrupole moments. Remarkably, this mechanism is found to act well beyond the h11/2 shell. PACS numbers: 21.10.Ky, 21.60.Cs, 32.10.Fn, 31.15.aj When first proposed the nuclear shell model was protons impinging on a tungsten rod produced low- to largely justified on the basis of magnetic-dipole proper- medium-energy neutrons inducing fission in a uranium ties of nuclei [1]. -
Radiation Glossary
Radiation Glossary Activity The rate of disintegration (transformation) or decay of radioactive material. The units of activity are Curie (Ci) and the Becquerel (Bq). Agreement State Any state with which the U.S. Nuclear Regulatory Commission has entered into an effective agreement under subsection 274b. of the Atomic Energy Act of 1954, as amended. Under the agreement, the state regulates the use of by-product, source, and small quantities of special nuclear material within said state. Airborne Radioactive Material Radioactive material dispersed in the air in the form of dusts, fumes, particulates, mists, vapors, or gases. ALARA Acronym for "As Low As Reasonably Achievable". Making every reasonable effort to maintain exposures to ionizing radiation as far below the dose limits as practical, consistent with the purpose for which the licensed activity is undertaken. It takes into account the state of technology, the economics of improvements in relation to state of technology, the economics of improvements in relation to benefits to the public health and safety, societal and socioeconomic considerations, and in relation to utilization of radioactive materials and licensed materials in the public interest. Alpha Particle A positively charged particle ejected spontaneously from the nuclei of some radioactive elements. It is identical to a helium nucleus, with a mass number of 4 and a charge of +2. Annual Limit on Intake (ALI) Annual intake of a given radionuclide by "Reference Man" which would result in either a committed effective dose equivalent of 5 rems or a committed dose equivalent of 50 rems to an organ or tissue. Attenuation The process by which radiation is reduced in intensity when passing through some material. -
Atomic Weights of the Elements 2013 (IUPAC Technical Report)
Pure Appl. Chem. 2016; 88(3): 265–291 IUPAC Technical Report Juris Meija*, Tyler B. Coplen, Michael Berglund, Willi A. Brand, Paul De Bièvre, Manfred Gröning, Norman E. Holden, Johanna Irrgeher, Robert D. Loss, Thomas Walczyk and Thomas Prohaska Atomic weights of the elements 2013 (IUPAC Technical Report) DOI 10.1515/pac-2015-0305 Received March 26, 2015; accepted December 8, 2015 Abstract: The biennial review of atomic-weight determinations and other cognate data has resulted in changes for the standard atomic weights of 19 elements. The standard atomic weights of four elements have been revised based on recent determinations of isotopic abundances in natural terrestrial materials: cadmium to 112.414(4) from 112.411(8), molybdenum to 95.95(1) from 95.96(2), selenium to 78.971(8) from 78.96(3), and thorium to 232.0377(4) from 232.038 06(2). The Commission on Isotopic Abundances and Atomic Weights (ciaaw.org) also revised the standard atomic weights of fifteen elements based on the 2012 Atomic Mass Evaluation: aluminium (aluminum) to 26.981 5385(7) from 26.981 5386(8), arsenic to 74.921 595(6) from 74.921 60(2), beryllium to 9.012 1831(5) from 9.012 182(3), caesium (cesium) to 132.905 451 96(6) from 132.905 4519(2), cobalt to 58.933 194(4) from 58.933 195(5), fluorine to 18.998 403 163(6) from 18.998 4032(5), gold to 196.966 569(5) from 196.966 569(4), holmium to 164.930 33(2) from 164.930 32(2), manganese to 54.938 044(3) from 54.938 045(5), niobium to 92.906 37(2) from 92.906 38(2), phosphorus to 30.973 761 998(5) from 30.973 762(2), praseodymium to 140.907 66(2) from 140.907 65(2), Article note: Sponsoring body: IUPAC Inorganic Chemistry Division Committee: see more details on page 289. -
Radiation Fields Using a Tepc*
XA00XC014 EUROPEAN LABORATORY FOR PARTICLE PHYSICS CERN/TIS-RP/95-14/CF A STUDY OF BUILD-UP EFFECTS IN HIGH-ENERGY RADIATION FIELDS USING A TEPC* M. Hofert1), A. Aroua2), A. V. Sannikov3) and G. R. Stevenson1) !) CERN, European Laboratory for Particle Physics, CH 1211 Geneva 23, Switzerland 2) IAR, Institute for Applied Radiophysics, CH 1015 Lausanne, Switzerland 3) IHEP, Institute for High-Energy Physics, RU 142284 Protvino, Russia * Supported by EU Research Contract FI3P-CT92-0026 Abstract A dose of 2 mSv close to the body surface of a pregnant woman is considered by ICRP to assure a dose limit of 1 mSv to the foetus. Such an assumption depends on the energy spectrum and composition of the external radiation field and it was tested in radiation fields containing high-energy particles similar to those found around high-energy particle accelerators and in air-craft. Measurements of dose and dose equivalent were performed as a function of wall thickness using a tissue-equivalent proportional counter (TEPC) in radiation fields at the CERN-EU Reference Radiation Facility. Results are presented both with respect to integral quantities and event size spectra. The decrease in dose and dose equivalent at a depth equivalent to that of the foetus was typically 10% in a high-energy stray radiation field and in the case of Pu- Be source neutrons amounted to only 30%. It is concluded that it would be prudent under such exposure conditions to limit the dose of a pregnant woman to 1 mSv in order to assure that the dose to the foetus remains below the same limit. -
Precision Mass Measurements for Studies of Nucleosynthesis Via the Rapid Neutron-Capture Process
Dissertation submitted to the Combined Faculties for the Natural Sciences and for Mathematics of the Ruperto-Carola University of Heidelberg, Germany for the degree of Doctor of Natural Sciences Put forward by Diplomant: Dinko Atanasov Born in: Yambol, Bulgaria Oral examination: 06. July 2016 Precision mass measurements for studies of nucleosynthesis via the rapid neutron-capture process Penning-trap mass measurements of neutron-rich cadmium and caesium isotopes Prof. Dr. Klaus Blaum Referees: PD Dr. Adriana P´alffy Zusammenfasung Obwohl die Theorie ¨uber die schnelle Neutronenanlagerung (r-Prozess) schon vor mehr als 55 Jahren entwickelt wurde, wird ¨uber den exakten Ort im Universum an dem dieser Prozess stattfindet noch rege debattiert. Theoretische Studien sagen voraus, dass der Verlauf des r-Prozesses gepr¨agtwird durch ¨außerstneutronenreiche Materie mit sehr asymmetrischen Proton-zu-Neutron Verh¨altnissen.Die aktuellen Kenntnisse ¨uber Eigenschaften dieser neutro- nenreichen Isotope, die dazu geeignet sind als Eingangsdaten f¨urStudien ¨uber den r-Prozess herangezogen zu werden, sind nur unzureichend oder gar nicht vorhanden. Die grundlegen- den Eigenschaften der Kerne, wie Bindungsenergie, Halbwertszeiten und Reaktionsquerschnitt spielen eine wichtige Rolle in den theoretischen Simulationen und k¨onnendiese beeinflussen oder sogar zu drastisch alternativen Ergebnissen f¨uhren. Um diese Theorien mit gemesse- nen Daten zu untermauern und die Produktion neutronenreicher Isotope zu verbessern, wurde an Forschungseinrichtungen wie ISOLDE am CERN, ein g¨anzlich bemerkenswerter Aufwand betrieben. Das Ziel dieser Dissertation ist es die experimentelle Arbeit zu beschreiben, welche n¨otigwar, um die Pr¨azisionsmassenmessungender neutronenreichen Isotope Cadmium (129−131Cd) und C¨asium(132;146−148Cs) zu erm¨oglichen. Die Messungen wurden an der Iso- topenfabrik ISOLDE am CERN mithilfe des aus vier Ionenfallen bestehenden Massenspek- trometers ISOLTRAP durchgef¨uhrt. -
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. -
4.48 Cadmium
IUPAC 4.48 cadmium Stable Relative Mole isotope atomic mass fraction 106 Cd 105.906 460 0.012 45 108 Cd 107.904 183 0.008 88 110 Cd 109.903 007 0.124 70 111 Cd 110.904 183 0.127 95 112 Cd 111.902 763 0.241 09 113 † Cd 112.904 408 0.122 27 114 Cd 113.903 365 0.287 54 116 † Cd 115.904 763 0.075 12 † Radioactive isotope having a relatively long half-life and a characteristic terrestrial isotopic composition that contributes significantly and reproducibly to the determination of the standard atomic weight of the element in normal materials . Half-lives of 113 Cd and 116 Cd are 8.04 × 10 15 years and 3 × 10 19 years, respectively. P.O. 13757, Research Triangle Park, NC (919) 485-8700 IUPAC 4.48.1 Cadmium isotopes in biology Metal accumulation is a threat to our world’s water systems and wildlife. As a way to measure the influence of heavy metals on wildlife with mass spectrometric techniques, some researchers use animal food enriched in specific cadmium isotopes . These experiments work by exposing the animals to a diet enriched in 106 Cd and/or other stable isotopes of metals (for example, 65 Cu and/or 62 Ni) for a period of time. Depending on the purpose of the experiment, the residence time of the food in the gut is determined and isotopic compositions of the gut and/or feces are measured via inductively coupled plasma mass spectrometry (ICP-MS). This information is used to measure bio-uptake (absorption and incorporation of a substance by living tissue) and accumulation rates of metals in an exposed animal [352, 353].