Bia So 1-4 Chuan Kich Thuoc. So 4.2019

Total Page:16

File Type:pdf, Size:1020Kb

Bia So 1-4 Chuan Kich Thuoc. So 4.2019 ISSN 1810-5408 Nuclear Science and Technology Volume 9, Number 4, December 2019 Published by VIETNAM ATOMIC ENERGY SOCIETY VIETNAM ATOMIC ENERGY INSTITUTE NUCLEAR SCIENCE AND TECHNOLOGY Volume 9, Number 4, December 2019 Editorial Board Editor-in-chief Tran Huu Phat (VINATOM) Executive Editors Vuong Huu Tan (VARANS) Tran Chi Thanh (VINATOM) Cao Dinh Thanh (VINATOM) Hoang Anh Tuan (VAEA) Editors Nguyen Kien Cuong (VINATOM) Le Hong Khiem (IOP) Nguyen Nhi Dien (VINATOM) Dao Tien Khoa (VINATOM) Nguyen Thi Kim Dung (VINATOM) Tran Hoai Nam (Duy Tan University) Ho Manh Dung (VINATOM) Dang Duc Nhan (VINATOM) Nguyen Nam Giang (VINATOM) Nguyen Hao Quang (VINATOM) Trinh Van Giap (VINATOM) Nguyen Mong Sinh (VINATOM) Le Ngoc Ha (108 Military Central Hospital) Tran Duc Thiep (IOP) Phan Son Hai (VINATOM) Dang Quang Thieu (VINATOM) Le Huy Ham (VAAS) Le Ba Thuan (VINATOM) Nguyen Quoc Hien (VINATOM) Nguyen Trung Tinh (VARANS) Le Van Hong (VINATOM) Tran Ngoc Toan (VINATOM) Nguyen Tuan Khai (VINATOM) Duong Thanh Tung (VARANS) Pham Dinh Khang (VINATOM) Nguyen Nu Hoai Vi (VARANS) Science Secretary Hoang Sy Than (VINATOM) .................................................................................................................................................................................................................... Copyright: ©2008 by the Vietnam Atomic Energy Society (VAES), Vietnam Atomic Energy Institute (VINATOM). Pusblished by Vietnam Atomic Energy Society, 59 Ly Thuong Kiet, Hanoi, Vietnam Tel: 84-24-39420463 Fax: 84-24-39424133 Email: [email protected] Vietnam Atomic Energy Institute, 59 Ly Thuong Kiet, Hanoi, Vietnam Tel: 84-24-39420463 Fax: 84-24-39422625 Email: [email protected] .................................................................................................................................................................................................................... Contents Bubble behavior in liquid-gas two-phase flow behind a cross-shaped obstacle in a vertical circular duct K. Takase, G. Kawasaki, K. Ueta……………………………………………..………………. 01 Evaluation of the Potential for Containment Bypass due to Steam Generator Tube Rupture in VVER-1000/V320 Reactor during Extended SBO sequence using SCDAP/RELAP5 code Nguyen Van Thai, Doan Manh Long, Tran Chi Thanh …………………………………… 09 Study on transmutation efficiency of the VVER-1000 fuel assembly with different minor actinide compositions Tran Vinh Thanh, Vu Thanh Mai, Hoang Van Khanh, Pham Nhu Viet Ha ……………. 18 Determination of in situ detection efficiency for IM-NAA of non-standard geometrical samples Nguyen Duy Quang, Trinh Van Cuong, Tran Tuan Anh, Ho Van Doanh, Nguyen Thi Tho, Ho Manh Dung……………………………………………………………………………. 27 Evaluating uncertainty of some radiation measurand using Monte Carlo method Bui Duc Ky, Nguyen Ngoc Quynh, Duong Duc Thang, Le Ngoc Thiem, Ho Quang Tuan, Tran Thanh Ha, Bui Thi Anh Duong, Nguyen Huu Quyet, Duong Van Trieu...... 34 Evaluation of image reconstruction algorithms in cone-beam computed tomography technique Tran Thuy Duong, Bui Ngoc Ha…………………………………………………………….. 41 Relative output factors of different collimation systems in truebeam STx medical linear accelerator Do Duc Chi, Tran Ngoc Toan, Robin Hill, Nguyen Do Kien …………………………….. 48 Nuclear Science and Technology, Vol.9, No. 4 (2019), pp. 01-08 Bubble behavior in liquid-gas two-phase flow behind a cross-shaped obstacle in a vertical circular duct K. Takase*, G. Kawasaki, K. Ueta *Department of Nuclear System Safety Engineering, Nagaoka University of Technology, Japan E-mail: [email protected] (Received 07 November 2019, accepted 26 December 2019) Abstract: Grid spacers installed in subchannels of fuel assemblies for nuclear reactors can promote heat transfer. However, the fluid velocity and bubble behavior are greatly affected as the cross- sectional area of the flow passage changes. Therefore, the void fraction distribution behind the obstacle that simulates the grid spacer shape simply was measured by using a wire mesh sensor (WMS) system. Moreover, a two-phase flow analysis was performed to investigate the effect of the obstacle on the bubble behavior in a vertical duct. Keywords: Bubbler, Two-phase flow, Obstacle, Vertical duct, WMS, Experiment, Analysis. I. INTRODUCTION simulated spacer was visually observed and the void fraction and interfacial velocity Clarifying two-phase characteristics distributions just behind the simulated in a nuclear reactor core is important in spacer was measured. particular to enhance the thermo-fluid safety of nuclear reactors. Moreover, correct data II. EXPERIMENTAL METHOD on bubbly flow in subchannels with spacers are needed in order to verify two-phase flow 1. Experimental Apparatus models in conventional nuclear safety The experimental apparatus mainly analysis codes and validate predicted data consists of a measuring section and by current CFD codes like a direct two- water/air supply lines and is shown in Fig. phase flow analysis code (Douce, et al., 1. The measuring section includes a vertical 2010). Spacers installed in subchannels of flow channel with a diameter of 58 mm fuel assemblies have the role of keeping the made of an acrylic resin, inlet and outlet interval between adjacent fuel rods constant. plenums, and an air injection nozzle with Similarly, in case of PWR the spacer has 120 injection holes with a diameter of 0.6 also the role as the turbulence promoter. mm. Water flows through the inlet plenum When the transient event occurs in a nuclear reactor, two-phase flow is generated by into the flow channel and goes up through boiling of water due to heating of fuel rods. the measuring section to the outlet plenum. Therefore, it is important to confirm the Air is supplied from the air injection nozzle Fig. 2 Observed into the flow channel. As a result, water is rising bubbles in a bubbly flow behavior around the spacer. flow channel The purpose of this study is to make the mixed with air and then a water-air two- effect of the spacer affecting the bubbly phase flow is formed as can be seen in Fig. flow clear and obtain code validation data. 2. Bubbly flow conditions are determined So bubble dynamics around the simply by both flow rates of water and air. ©2019 Vietnam Atomic Energy Society and Vietnam Atomic Energy Institute BUBBLE BEHAVIOR IN LIQUID-GAS TWO-PHASE FLOW BEHIND A CROSS-SHAPED… f58 mm Wire mesh Sensor Cross- direction Flow shaped obstacle 2600 mm 2600 High speed Camera 1150 mm 1150 20 mm or 100 mm 100 or mm 20 Air nozzle Fig. 1. Outline of an experimental apparatus Fig. 2. Observed rising bubbles in a flow channel 2. Wire-Mesh Sensor System temperatures of water and air are measured at the water/air supply piping lines. The void fraction distribution at the horizontal cross- section in the flow channel is The WMS can obtain the void fraction measured with a wire-mesh sensor (WMS) distribution in a cross-section of the flow channel system (Prasser et al., 1998; 2000; 2001). by measuring the electric current from the Complicated behavior of an interface between transmitter-side wire layer through the fluid to the water and air of each bubble is visually receiver-side wire layer. Both wire layers consist observed with a high speed camera (HSC). of nine wires respectively and are installed in the Moreover, two-phase pressure loss is measured flow channel with the distance of 3 mm in the with seven differential pressure transducers flow direction. The wire diameter is 0.3 mm. installed in the arbitrary locations in the Appearance and measuring wires of the WMS vertical direction of the flow channel. In are shown in Fig. 3. A mearing method with addition, both flow rates, pressures and the WMS is as follows. Layout of each wire of transmitter and Clipped layout of Appearance of a wire-mesh sensor receiver in the vertical direction each wire (Dimension: mm) in the horizontal Fig. 3. Appearance and layout directionof a wire -mesh sensor in a circular flow channel 2 K. TAKASE et al. 1) Current is given to the transmitter-side Moreover, the cross-correlation wire layer; coefficient used to obtain the interfacial velocity is obtained from the relationship 2) The current flows from the transmitter- between both data measured by a couple of side wire layer through the fluid to the the WMS layers and is expressed by the receiver-side wire layer; following equation. 3) The voltage is measured at the location where each wire intersects; and, n xtt x y y 4) Void fraction between both wires cor() t1 (3) n is obtained. 22 xtt x y y The following equation is used for t1 the conversion from the voltage to the Here, x and y represent time series void void fraction. fraction data measured with the WMS UU installed upstream in the flow direction and L i, j (1) ij, the WMS installed downward. The n shows UULG the number of comparison data. The cross- Here, is the local void fraction, (i, j) correlation coefficient, cor() has the value is the position where two wires intersect in from -1 to 1, and it shows 1 when both data of the cross-section of the flow channel, U [V] x and y have the positive correlation, -1 when is the voltage measured by the WMS at two- those are the negative correlation, and 0 when phase flow condition, Each of UL [V] and those have no correlation. UG [V] is the voltage measured by the WMS at the single-phase flow condition of liquid or gas. On the other hand, gas-liquid interface velocity is determined using the time-series void fraction data measured by a couple of the WMS layers which are installed upstream and downstream of the flow channel. Two void fraction data by both WMS layers are compared. In Fig 4, time difference, , in case that the cross-correlation coefficient between both void fraction data shows the highest match is identified. Finally, the gas-liquid interface velocity, ub, is calculated by Eq. (2) using S and . Here, S is the distance between both receiver-side wire layers. S u (2) Fig. 4. Example of time variation of void fraction b data at the different vertical positions 3 BUBBLE BEHAVIOR IN LIQUID-GAS TWO-PHASE FLOW BEHIND A CROSS-SHAPED… 3.
Recommended publications
  • Health Physics Education Reference Book
    HEALTH PHYSICS EDUCATION REFERENCE BOOK 2010 - 2011 Health Physics Society Academic Education Committee Updated June 2010 1. Bloomsburg University Pennsylvania BS 2. Clemson University South Carolina MS PhD 3. Colorado State University Colorado MS PhD 4. Duke University North Carolina MS PhD 5. Francis Marion University South Carolina BS 6. Idaho State University Idaho AA BS MS PhD 7. Illinois Institute of Technology Illinois MS 8. Linn State Technical College Missouri AA 9. Louisiana State University Louisiana MS PhD 10. Ohio State University Ohio MS PhD 11. Oregon State University Oregon BS MS PhD 12. Purdue University Indiana BS MS PhD 13. Rensselaer Polytechnic Institute New York BS MS PhD 14. San Diego State University California MS 15. Texas A&M University Texas BS MS PhD 16. Texas State Technical College Texas AA 17. Thomas Edison State College AS BS 18. University of Cincinnati Ohio MS PhD 19. University of Florida Florida BS MS PhD 20. University of Massachusetts Lowell Massachusetts BS MS PhD 21. University of Michigan Michigan BS MS PhD 22. University of Missouri-Columbia Missouri MS PhD 23. University of Nevada Las Vegas Nevada BS MS 24. University of Tennessee Tennessee BS MS PhD 25. Vanderbilt University Tennessee MS PhD 26. Virginia Commonwealth University Degree Programs Recognized by the Accreditation Board for Engineering and Technology (ABET) in Health Physics under ABET’s Applied Science Accreditation Commission (ASAC) Bloomsburg University Health Physics (BS) (2006) Clemson University Environmental Health Physics (MS) (2005) Colorado State University Health Physics (MS) (2007) Idaho State University Health Physics (BS) (2003) Idaho State University Health Physics (MS) (2003) Oregon State University Radiation (2004) University of Nevada Las Vegas Health Physics (MS) (2003) Degree Programs Recognized by the Accreditation Board for Engineering and Technology (ABET) in Radiological Engineering under ABET’s Engineering Accreditation Commission (EAC) Texas A&M University Radiological Health Engineering (BS) (1987) 1.
    [Show full text]
  • The Impact of Partitioning and Transmutation on the Risk Assesment of a Spent Nuclear Fuel
    h/e/-se SE0608415 The Impact of Partitioning and Transmutation on the Risk Assesment of a Spent Nuclear Fuel Naima Amrani and Ahmed Boucenna UFAS University Physics Department Faculty of sciences Setif 19000 ALGERIA I. INTRODUCTION Nuclear power produces steadily a mass of spent fuel which contains a part from the short lived fission products, a significant amount of actinides and fission products with height toxicity and long half-lives. These nuclides constitute the long-term radiotoxic inventory which remains as a hazard far beyond human perception. The reprocessing recycles most of the major actinides (Uranium and Plutonium), while the Minor Actinides (MA) (mainly Neptunium: Np, Americium: Am and Curium: Cm) with half lives up to 2 million years remain with the fission products which are vitrified before being buried in deep repositories. Partitioning of the minor actinides and some of the fission products is an efficient method to reduce the long term radiotoxicity of the residual waste components with a factor proportional to the separation yield. The improved minor actinide nuclides would be recycled into a fuel cycle activities and returned to the reactor inventory of fissile and fertile material for transmutation to short lived isotopes. Progressively the MAs and some long-lived fission product (LLFP) could be burn up out. This option would reduce the long term contamination hazard in the high-level waste and shorten the time interval necessary to keep the actinides containing wastes confined in a deep geologic repository. Partitioning and Transmutation (P&T) is, in principal, capable of reducing the radiotoxicity period, while a number of practical difficult remain to be surmounted.
    [Show full text]
  • Plutonium Incorporation in Phosphate and Titanate Ceramics for Minor Actinide Containment
    Journal of Nuclear Materials 352 (2006) 233–240 www.elsevier.com/locate/jnucmat Plutonium incorporation in phosphate and titanate ceramics for minor actinide containment X. Deschanels a,*, V. Picot a, B. Glorieux b, F. Jorion a, S. Peuget a, D. Roudil a, C. Je´gou a, V. Broudic a, J.N. Cachia a, T. Advocat a, C. Den Auwer a, C. Fillet a, J.P. Coutures b, C. Hennig c, A. Scheinost c a DIEC/LMPA, CEA/DEN Valrho Marcoule, BP 17171, 30207 Bagnols-sur-Ce`ze cedex, France b PROMES-CNRS Tecnosud, Rambla de la Thermodynamique, 66100 Perpignan, France c ROBL-CRG, ESRF, BP 220, 38043 Grenoble, France Abstract Two ceramics, zirconolite and a monazite–brabantite solid solution (MBss) were studied for the immobilization of minor actinides (Np, Am, Cm) produced by reprocessing spent fuel. Monoclinic zirconolite (CaZrTi2O7) is a fluorite deriv- ative structure and is the primary actinide host phase in Synroc (a titanate composite). Monazite (LnPO4, where Ln = La, Ce, Nd, Gd, etc.) is a monoclinic orthophosphate containing trivalent cations, and brabantite (Ca0.5An0.5PO4) is an iso- structural monazite compound containing tetravalent cations (An = Th and U). The nominal composition of the ceramics studied in this work is (Ca0.87Pu0.13)Zr(Al0. 26Ti1.74)O7 for zirconolite and (Ca0.09Pu0.09La0.73Th0.09)PO4 for the monazite– brabantite solid solution. These formulas correspond to 10 wt% PuO2 loading in each material. XANES spectroscopy showed that the plutonium is tetravalent in zirconolite and trivalent in MBss. Thorium, another tetravalent cation, can be incorporated at 10 wt% ThO2 in MBss.
    [Show full text]
  • Los Alamos NATIONAL LABORATORY
    — . .. ,. ~ - /3~5Y” m5 ~“3 CIC-14 REPORT CQUECTW REPRODUCTION COPY Measurement and Accounting of the Minor Adinides Produced in Nuclear Power Reactors Los Alamos NATIONAL LABORATORY .i,os Alarnos National Laboratory is operated by the University of Cal~ornia for the United States Department of Energy under contract W-7405-ENG-36. Etlifeci by Paul IV. Fknriksen, Group ClC-l Prepared by Celirza M. CMz, Group lVIS-5 This work was supported by the U.S. Department of Energy, Ofice of lVonprol~eration and National Security, Ofice of Safeguards and Security, An Ajirmativc AcfionfEqual Opporfunify Employer This report waspreparedasan accountof worksponsoredby an agencyof theUnited States Govemrnent. NeitherTheRegentsof fhe Universityof Cal@rnia,the United Stafes Government norany agencythereof,norany of theiremployees,makesany warranty,express or implied,or assumesany legalliabilityor responsibilify~ortheaccuracy,completeness, or usefulness of any information, apparatus, product, or process disclosed,orrepresentsthat its use wouldnof infringe privately owned rights. Referenceherein to any speczfic commercial product, process, or seru”ce by trade name, trademark, manufacturer, or otherwise, doesnot necessarily constitute or imply its endorsement, recommendation, or favoring by The Regents of the University of California, fhe LInifedStates Government, or any agency thereof. The views and opinions of aufhors expressed herein do nof necessarily sfate or r~ect those of The Regents of the University of Calt@nia, the Unifed Sfates Government, or any agency thereo$ The Los A[amos National Laboratory strongly supports academic freedom and a researcher’s right to publish; therefore, the .!..aboratory as an institution doesnot endorse the viewpoint of a publication or guarantee its technical correctness. LA-13054-MS UC-700 Issued: January 1996 Measurement and Accounting of the Minor Actinides Produced in Nuclear Power Reactors J.
    [Show full text]
  • Emergence of Californium As the Second Transitional Element in the Actinide Series
    ARTICLE Received 28 Nov 2014 | Accepted 3 Mar 2015 | Published 16 Apr 2015 DOI: 10.1038/ncomms7827 OPEN Emergence of californium as the second transitional element in the actinide series Samantha K. Cary1, Monica Vasiliu2, Ryan E. Baumbach3, Jared T. Stritzinger1, Thomas D. Green1, Kariem Diefenbach1, Justin N. Cross1, Kenneth L. Knappenberger1, Guokui Liu4, Mark A. Silver1, A. Eugene DePrince1, Matthew J. Polinski1, Shelley M. Van Cleve5, Jane H. House1, Naoki Kikugawa6, Andrew Gallagher3, Alexandra A. Arico1, David A. Dixon2 & Thomas E. Albrecht-Schmitt1 A break in periodicity occurs in the actinide series between plutonium and americium as the result of the localization of 5f electrons. The subsequent chemistry of later actinides is thought to closely parallel lanthanides in that bonding is expected to be ionic and complexation should not substantially alter the electronic structure of the metal ions. Here we demonstrate that ligation of californium(III) by a pyridine derivative results in significant deviations in the properties of the resultant complex with respect to that predicted for the free ion. We expand on this by characterizing the americium and curium analogues for comparison, and show that these pronounced effects result from a second transition in periodicity in the actinide series that occurs, in part, because of the stabilization of the divalent oxidation state. The metastability of californium(II) is responsible for many of the unusual properties of californium including the green photoluminescence. 1 Department of Chemistry and Biochemistry, Florida State University, Tallahassee, Florida 32306, USA. 2 Department of Chemistry, The University of Alabama, Tuscaloosa, Alabama 35487, USA. 3 National High Magnetic Field Laboratory, Tallahassee, Florida 32310, USA.
    [Show full text]
  • Curium in Space
    ROBIN JOHANSSON Curium in Space KTH Royal Institute of Technology Master Thesis 2013-05-05 Abstract New technology has shown the possibility to use a miniature satellite in conjunction with an electric driven engine to make a spiral trajectory into space from a low earth orbit. This report has done an investigation of the new technique to produce power sources replacing solar panels which cannot be used in missions out in deep space. It is in essence an alternative use of curium among the many proposals on how to handle the intermediate stored used nuclear fuel or once through nuclear fuel as some people prefer to call it. The idea of sending radioactive used nuclear fuel into outer space has been considered before. There was a proposal, for example, to load a space shuttle with radioactive material. This could have serious consequences to the nearby population in the event of a major malfunction to the shuttle. The improvement to this old idea is to use a small satellite with only a fraction of the spent fuel. With this method and other technological advances, it is possible to further reduce the risk of contamination in the event of a crash. This report has looked into the nuclear energy production of Sweden and the current production of transuranium elements (Pu, Np, Am and Cm). The report has also focused on the curium (Cm) part of the transuranium elements, which is the most difficult to recycle in a fast neutron spectra. The physical property of curium reduces many of the safety parameters in the reactor as it is easily transmutated into californium, which is a high neutron emitter.
    [Show full text]
  • Composition of Spent Nuclear Fuel (Standard PWR 33GW/T, 10 Yr. Cooling) Most of the Hazard Stems from Pu, MA and Some LLFP When
    Spent fuel and radiotoxicity 1/3 Composition of Spent Nuclear Fuel (Standard PWR 33GW/t, 10 yr. cooling) 1 tonne of SNF contains: 955.4 kg U 8,5 kg Pu Minor Actinides (MAs) 0,5 kg 237Np 0,6 kg Am 0,02 kg Cm Long-Lived fission Most of the hazard stems from Pu, MA and some Products (LLFPs) 0,2 kg 129I LLFP when released into the environment, and 0,8 kg 99Tc their disposal requires isolation in stable deep 0,7 kg 93Zr geological formations. 0,3 kg 135Cs Short-Lived fission A measure of the hazard is provided by the products (SLFPs) radiotoxicity arising from their radioactive 1 kg 137Cs nature. 0,7 kg 90Sr Stable Isotopes 10,1 kg Lanthanides 21,8 kg other stable Spent fuel and radiotoxicity 2/3 Paths of Minor actinide formation in the U-Pu Cycle Z 249Cf 250Cf 251Cf 252Cf 249Bk 250Bk 242Cm 243Cm 244Cm 245Cm 246Cm 247Cm 248Cm 249Cm 241Am 242Am 243Am 244Am 239Pu 240Pu 241Pu 242Pu 243Pu - β 239Np β- dn (2 d) j n j j n 238U 239U j aj j K K K dt K +n N Spent fuel and radiotoxicity 3/3 Evolution of the radiotoxic inventory, expressed in sievert per tonne of initial heavy metal (uranium) (Sv/ihmt) of UOX spent fuel unloaded at 60 GW d/t, versus time (years). 1.00E+07 Total 1.00E+06 Minor Actinides & Decay Products 1.00E+05 "Uranium Ore" 1.00E+04 Plutonium & Decay Products Fission Products Radiotoxicity of Natural Uranium and Decay Products Radiotoxicity (Sv/MT Natural Uranium) (Sv/MT Natural Radiotoxicity 1.00E+03 Uranium & Decay Products 1.00E+02 1.00E+02 1.00E+03 1.00E+04 1.00E+05 1.00E+06 Years after Spent Fuel Discharge What is Partitioning &Transmutation? Use of nuclear reactions to transform long lived nuclides into stable or short-lived nuclides (transmutation) Chemical separation of these nuclides from HLW is an inevitable ingredient for transmutation (partitioning) Objectives: Alleviation of the burden of a final disposal and minimization of long-lived nuclides in HLW P/T applies to TRU (Pu and Minor Actinides) and Long Lived Fission Products.
    [Show full text]
  • Burning of Actinides: a Complementary Waste Management Option?
    TOPICAL REPORTS Burning of actinides: A complementary waste management option? Partitioning and transmutation of actinides and fission products may serve as an additional tool in waste management strategies by L.H. Baetsle W'e orldwide nuclear electric capacity amounts The vitrified waste is stored in engineered to nearly 340 gigawatts-electric (GWe) and facilities awaiting final disposal in underground produces spent fuel roughly amounting to 9000 repositories. Disposal of vitrified high-level tonnes heavy metal (tHM) per year. Each tonne waste (HLW) containing the minor actinides, or of spent fuel contains about 10 kg of trans- spent fuel with plutonium and minor actinides, uranium (TRU) actinides, of which 0.8 kg are are from the environmental point of view very minor actinides, and 30 kg of fission products, similar at least during the first millennia. Beyond including 4 kg that are long-lived nuclei (having 10 000 years — the technical lifetime of an half-lives greater than 30 years). underground repository — spent fuel with its full The fate of the spent fuel depends to a great load of plutonium becomes the dominant en- extent on the national fuel cycle policy. For one- vironmental hazard. half of the world's capacity of nuclear power plants, the policy calls for reprocessing, plu- tonium recovery, vitrification of residues, and Interest in partitioning and transmutation disposal of wastes. Among the countries follow- ing this course are France, United Kingdom, Two decades ago the question was already Japan, Germany, Belgium, Switzerland, the raised: Can we avoid the long-term hazard as- Commonwealth of Independent States, and sociated with TRU actinides and long-lived fis- countries formerly in the Soviet alliance.
    [Show full text]
  • Nolan E. Hertel Professor 3/25/2019
    Nolan E. Hertel Professor 3/25/2019 CV Table of Contents Section Description Page I. Earned Degrees 2 II. Employment History 2 III. Honors and Awards 3 IV. Research, Scholarship, and Creative Activities 3 IV.A. Published Books, Chapters, and Edited Volumes 3 IV.B. Refereed Publications and Submitted Articles 4 IV.C. Other Publications and Creative Products 19 IV.D. Presentations 27 IV.E. Grants and Contracts 44 IV.F. Other Scholarly and Creative Accomplishments 53 IV.G. Societal and Policy Impacts 53 IV.H Other Professional Activities 53 V. Education 55 V.A. Courses Taught 55 V.B. Individual Student Guidance 56 V.C. Educational Innovations and Other Contributions 66 VI. Service 68 VI.A. Professional Contributions 68 VI.B. Public and Community Service 75 VI.C. Institute Contributions 76 1 NOLAN E. HERTEL PROFESSOR OF NUCLEAR AND RADIOLOGICAL ENGINEERING G. W. WOODRUFF SCHOOL OF MECHANICAL ENGINEERING MARCH 25, 2019 I. EARNED DEGREES Ph.D., 1979, University of Illinois at Urbana-Champaign, Nuclear Engineering (co-Advisors: B. W. Wehring and J. J. Dorning) M.S., 1975, Texas A&M University, Nuclear Engineering (Advisor: James B. Smathers) B.S., 1973, Texas A&M University, Nuclear Engineering II. EMPLOYMENT HISTORY Professor, Georgia Institute of Technology, G. W. Woodruff School of Mechanical Engineering, Nuclear and Radiological Engineering Program, 7/1997 - present Interim Chair of the Nuclear and Radiological Engineering and Medical Physics Programs, G. W. Woodruff School of Mechanical Engineering, 7/01/2016 – 7/31/2017. Acting Director, Joint Faculty Appointment, Center for Radiation Knowledge, Environmental Sciences Division, Oak Ridge National Laboratory, 9/1/13-present.
    [Show full text]
  • Impact of Fissile Minor Actinides on the Criticality Safety of Transport of Fissile Material
    Proceedings of the 18th International Symposium on the Packaging and Transportation of Radioactive Materials PATRAM 2016 September 18-23, 2016, Kobe, Japan Paper No. 2030 Impact of fissile minor actinides on the criticality safety of transport of fissile material Mathieu Milin Nadège Kodratoff IRSN, France URANUS, France Wim Haeck IRSN, France Abstract In the current IAEA regulation for the safe transport of radioactive material [1] and all previous editions of this regulation, the fissile materials are defined as the materials containing any of the 4 following nuclides 233U, 235U, 239Pu and 241Pu. It is well-known that other nuclides are able to sustain a fission chain reaction and that some of them have a lower subcritical mass limit than the four usual fissile nuclides, for example 242mAm, 243Cm and 251Cf. In cases where sufficient quantities of these nuclides would be present in a material, the guidance of the regulation [2] advices to perform a criticality safety assessment as per the requirements of paragraphs 673-686. When these minor actinides are not separated from fission products, uranium or plutonium (for example, in irradiated UOX or MOX fuel), they have no impact on nuclear criticality safety and the formulation of SSR-6 is acceptable. However, if these fissile minor actinides come from an enhanced separation process, they could have a significant impact on reactivity even for limited quantities (several grams), in particular for some nuclides. Moreover, even if many minor actinides have a significant subcritical mass limit (much higher than 235U), when these nuclides are irradiated (for example, as experimental fuel), it becomes more complicated to justify subcriticality if their initial mass is important.
    [Show full text]
  • On Minor Actinide Transmutation in Hard Neutron Spectra
    Why Faster is Better - On Minor Actinide Transmutation in Hard Neutron Spectra DANIEL WESTLÉN Doctoral Thesis Stockholm, Sweden 2007 TRITA-FYS KTH ISSN 0280-316X School of Engineering Sciences ISRN KTH/FYS/--07:05--SE SE-106 91 Stockholm ISBN 978-91-7178-567-1 SWEDEN Akademisk avhandling som med tillstånd av Kungl Tekniska högskolan framlägges till offentlig granskning för avläggande av teknologie doktorsexamen i fysik fredagen den 2007-02-23 klockan 14.15 i hörsal F3, Lindstedtsvägen 26. © Daniel Westlén, January 2007 Tryck: Universitetsservice US AB ii Abstract In this thesis, options for efficient transmutation of transuranium elements are discussed. The focus is on plutonium, americium and curium mainly because of their long-term contribution to the radiotoxicity of spent nuclear fuel. Two innovative helium-cooled core designs are proposed, dedicated to the transmutation of actinides. The performance of the more promising of the two is studied in realistic transient fuel cycle scenarios. During the 1150 day irradiation cycle, a minor actinide consumption of 355 kg/GWth·year is achieved. An analysis of the efficiency of spallation neutron sources in helium-cooled cores is also performed. It is shown that the proton source efficiency, ψ∗, is improved by about 10% when helium is used as coolant, rather than lead-bismuth eutectic. Further, a proposal is made to transmute actinides in the upper part of a BWR core. A net consumption of transuranics is shown possible in the BWR park already when 50% of the BWR fuel is of the proposed evolutionary type. The thesis concludes that efficient transmutation of transuranic elements in dedicated helium-cooled subcritical cores is possible.
    [Show full text]
  • Calculated Investigation of Actinide Transmutation in the Bor-60 Reactor
    CALCULATED INVESTIGATION OF ACTINIDE TRANSMUTATION IN THE BOR-60 REACTOR I.Yu. Zhemkov, O.V. Ishunina, I.V. Yakovleva State Scientific Centre of the Russian Federation Research Institute of Atomic Reactors Dimitrovgrad, Russia ABSTRACT In the course of reactor operation the formation of fission products and accumulation of minor-actinides and plutonium take place in the nuclear fuel. These materials define the radiation hazard to a great extent. Of one possible ways lowering the activity of irradiated nuclear fuel is transmutation of long-lived radioactive isotopes in the stable or short-lived ones, that allows to facilitate the problem of the high-level waste and to improve the efficiency of nuclear fuel use at the expense of its recycling and burnup increasing. INTRODUCTION ofthe possible directions of reducing the general activity (in particular, its long-lived component), that allows to With the development of nuclear energy the available facilitate the problem of the high-level waste in nuclear power resources have been greatly extended at the engineering and to improve the efficiency of nuclear fuel expense of uranium, but with provision of the possibility usage at the expense of its recycling and utilisation of of nuclear fuel breeding in fast reactors they have become plutonium recourses. practically unlimited. But, nuclear energy has set up new However transmutation of plutonium and minor- problems, in particular radioactive waste. actinides must not be considered in isolation from the At present the problem of nuclear waste is one of the process of conversion and decontamination of nuclear most acute in nuclear power engineering, which attracted wastes, as well as possible incineration of the most increased attention both on the part of specialists and dangerous fission products, since at a specific stage they public.
    [Show full text]