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Physics of plutonium recycling. 6 : a report by the working party on the physics of plutonium recycling of the NEA Nuclear Science Committee : Multiple Pu recycling in advanced PWRs PDF

162 Pages·2002·0.983 MB·English
by  OECD
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Preview Physics of plutonium recycling. 6 : a report by the working party on the physics of plutonium recycling of the NEA Nuclear Science Committee : Multiple Pu recycling in advanced PWRs

Nuclear Science Physics of Plutonium Recycling Volume VI Multiple Pu Recycling in Advanced PWRs NUCLEAR ENERGY AGENCY ORGANISATION FOR ECONOMIC CO-OPERATION AND DEVELOPMENT ORGANISATION FOR ECONOMIC CO-OPERATION AND DEVELOPMENT Pursuant to Article 1 of the Convention signed in Paris on 14th December 1960, and which came into force on 30th September 1961, the Organisation for Economic Co-operation and Development (OECD) shall promote policies designed: − to achieve the highest sustainable economic growth and employment and a rising standard of living in Member countries, while maintaining financial stability, and thus to contribute to the development of the world economy; − to contribute to sound economic expansion in Member as well as non-member countries in the process of economic development; and − to contribute to the expansion of world trade on a multilateral, non-discriminatory basis in accordance with international obligations. The original Member countries of the OECD are Austria, Belgium, Canada, Denmark, France, Germany, Greece, Iceland, Ireland, Italy, Luxembourg, the Netherlands, Norway, Portugal, Spain, Sweden, Switzerland, Turkey, the United Kingdom and the United States. The following countries became Members subsequently through accession at the dates indicated hereafter: Japan (28th April 1964), Finland (28th January 1969), Australia (7th June 1971), New Zealand (29th May 1973), Mexico (18th May 1994), the Czech Republic (21st December 1995), Hungary (7th May 1996), Poland (22nd November 1996), Korea (12th December 1996) and the Slovak Republic (14 December 2000). The Commission of the European Communities takes part in the work of the OECD (Article 13 of the OECD Convention). NUCLEAR ENERGY AGENCY The OECD Nuclear Energy Agency (NEA) was established on 1st February 1958 under the name of the OEEC European Nuclear Energy Agency. It received its present designation on 20th April 1972, when Japan became its first non-European full Member. NEA membership today consists of 28 OECD Member countries: Australia, Austria, Belgium, Canada, Czech Republic, Denmark, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Japan, Luxembourg, Mexico, the Netherlands, Norway, Portugal, Republic of Korea, Slovak Republic, Spain, Sweden, Switzerland, Turkey, the United Kingdom and the United States. The Commission of the European Communities also takes part in the work of the Agency. The mission of the NEA is: − to assist its Member countries in maintaining and further developing, through international co-operation, the scientific, technological and legal bases required for a safe, environmentally friendly and economical use of nuclear energy for peaceful purposes, as well as − to provide authoritative assessments and to forge common understandings on key issues, as input to government decisions on nuclear energy policy and to broader OECD policy analyses in areas such as energy and sustainable development. Specific areas of competence of the NEA include safety and regulation of nuclear activities, radioactive waste management, radiological protection, nuclear science, economic and technical analyses of the nuclear fuel cycle, nuclear law and liability, and public information. The NEA Data Bank provides nuclear data and computer program services for participating countries. In these and related tasks, the NEA works in close collaboration with the International Atomic Energy Agency in Vienna, with which it has a Co-operation Agreement, as well as with other international organisations in the nuclear field. © OECD 2002 Permission to reproduce a portion of this work for non-commercial purposes or classroom use should be obtained through the Centre français d’exploitation du droit de copie (CCF), 20, rue des Grands-Augustins, 75006 Paris, France, Tel. (33-1) 44 07 47 70, Fax (33-1) 46 34 67 19, for every country except the United States. In the United States permission should be obtained through the Copyright Clearance Center, Customer Service, (508)750-8400, 222 Rosewood Drive, Danvers, MA 01923, USA, or CCC Online: http://www.copyright.com/. All other applications for permission to reproduce or translate all or part of this book should be made to OECD Publications, 2, rue André-Pascal, 75775 Paris Cedex 16, France. FOREWORD The OECD/NEA Working Party on the Physics of Plutonium Fuels and Innovative Fuel Cycles (WPPR) was established in 1993 and reports to the OECD/NEA Nuclear Science Committee. Its main activity has been to analyse physics code benchmarks for problems related to the physics of plutonium fuels. Past volumes of published work have examined the physics of plutonium-fuelled pressurised water reactors (PWRs), as well as the physics of metal- and oxide-fuelled fast reactors. Some of the questions that the Working Group has attempted to address in the present and previous volumes include: • What is the effect on the physics of the degradation in plutonium fissile quality that occurs with increasing burn-up and age of spent fuel? • What is the impact on the physics of multiple recycling of plutonium if MOX assemblies are themselves reprocessed? What are the limitations associated with multiple recycling? Is there a point beyond which multiple recycling becomes no longer practicable in the present generation of PWRs? • Are the present nuclear data libraries and neutronics codes capable of predicting the physics performance of MOX made from plutonium derived from high burn-up and/or multiple- recycling scenarios? • Is thermal MOX recycling ultimately compatible with a fast-reactor fuel cycle? Can fast reactors be used in a flexible manner to address whatever requirements there might be to consume plutonium from a thermal MOX programme? Can plutonium-burning fast reactors be changed to plutonium breeding to maintain self-sufficiency in the longer term? • How do the nuclear codes compare with real data from experiments? The “Physics of Plutonium Recycling” series currently comprises the following titles: • Volume I: Issues and Perspectives (OECD/NEA, 1995); • Volume II: Plutonium Recycling in Pressurised Water Reactors (OECD/NEA, 1995); • Volume III: Void Reactivity Effect in Pressurised Water Reactors (OECD/NEA, 1995); • Volume IV: Fast Plutonium Burner Reactors: Beginning of Life (OECD/NEA, 1995); • Volume V: Plutonium Recycling in Fast Reactors (OECD/NEA, 1996); • Volume VI: Multiple Plutonium Recycling in Advanced PWRs (OECD/NEA, 2002). 3 Volumes VII and VIII, in preparation, will be devoted to a theoretical benchmark of a boiling water reactor (BWR) assembly containing mixed-oxide fuel rods, and to plutonium fuel in high- temperature reactors. While all of the earlier work consisted of theoretical benchmarks comparing different nuclear codes and nuclear data libraries, comparisons against experimental measurements were made possible by SCK-CEN using data from the VENUS-2 reactor. The VENUS-2 data concerned an experimental mock-up of a PWR core containing UO and mixed-oxide (MOX) assemblies. The results of this 2 benchmark were published in Benchmark on the VENUS-2 MOX Core Measurements (OECD/NEA, 2000). The benchmark was carried out under the joint auspices of the WPPR and the Task Force on Reactor-based Plutonium Disposition (TFRPD). Another benchmark was undertaken for three critical core configurations of the KRITZ reactor: two with UO fuel and one with MOX fuel. Measurements 2 were performed for room temperature as well as elevated temperatures (~245°C). The results are due to be published soon. 4 TABLE OF CONTENTS FOREWORD................................................................................................................................. 3 CONTRIBUTORS......................................................................................................................... 7 BENCHMARK PARTICIPANTS............................................................................................... 8 EXECUTIVE SUMMARY........................................................................................................... 9 Chapter 1. INTRODUCTION....................................................................................................... 11 Chapter 2. BENCHMARK SPECIFICATION........................................................................... 15 Chapter 3. PARTICIPANTS AND METHODS.......................................................................... 27 Chapter 4. PRESENTATION OF RESULTS............................................................................. 29 Annex to Chapter 4 – Energy per reaction................................................................... 75 Chapter 5. DISCUSSION AND INTERPRETATION OF RESULTS...................................... 79 Chapter 6. RESULTS OF THE SPECIAL BENCHMARK ON PWR MOX PIN CELLS.... 89 Annex 1 to Chapter 6 – Specifications of the new benchmark to compare MCNP, WIMS, APPOLLO2, CASMO4 and SRAC................. 111 Annex 2 to Chapter 6 – Effect of different state-of-the-art nuclear data libraries on the PWR MOX pin cells benchmark of Chapter 6............. 113 Chapter 7. CONCLUSIONS......................................................................................................... 115 REFERENCES.............................................................................................................................. 117 APPENDIX A – Phase II – Benchmark specification................................................................... 119 APPENDIX B – List of participants (addresses)........................................................................... 143 APPENDIX C – List of symbols and abbreviations...................................................................... 151 APPENDIX D – Corrigendum for previous volumes.................................................................... 153 5 CONTRIBUTORS CHAIR K. Hesketh BNFL UK SECRETARY E. Sartori OECD/NEA PRINICPAL AUTHORS M. Delpech CEA France K. Hesketh BNFL UK D. Lutz IKE Germany E. Sartori OECD/NEA PROBLEM SPECIFICATION M. Delpech CEA France SPECIAL CONTRIBUTION G. Schlosser Siemens/KWU Germany DATA COMPILATION AND ANALYSIS M. Delpech CEA France I. Champtiaux CEA France M. Goutefarde CEA France M. Juanola CEA France SPECIAL STUDY (CHAPTER 6) S. Cathalau CEA France D. Lutz IKE Germany W. Bernnat IKE Germany M. Mattes IKE Germany T.T.J. M. Peeters ECN The Netherlands Y. Peneliau CEA France A. Puill CEA France H. Takano JAERI Japan EDITOR K. Hesketh BNFL UK TEXT PROCESSING AND LAYOUT A. McWhorter OECD/NEA H. Déry OECD/NEA 7 BENCHMARK PARTICIPANTS Name Establishment Country MALDAGUE, Thierry Belgonucléaire Belgium HOEJERUP C. Frank Risø Denmark BARBRAULT Patrick EDF-Clamart France VERGNES Jean EDF-Clamart DELPECH Marc CEA-Cadarache COSTE Mireille CEA-Saclay LEE Yi-Kang CEA-Saclay PENELIAU Yannick CEA- Saclay PUILL André CEA- Saclay ROHART Michelle CEA- Saclay TSILANIZARA Aimé CEA- Saclay POINOT-SALANON Christine FRAMATOME HESSE Ulrich GRS Germany MOSER Eberhard GRS LEHMANN Sven U-Braunschweig BERNNAT Wolfgang U-Stuttgart-IKE LUTZ Dietrich U- Stuttgart -IKE MATTES Margerete U- Stuttgart -IKE SCHWEIZER M. U- Stuttgart -IKE KANEKO K. ITIRO Japan AKIE Hiroshi JAERI TAKANO Hideki JAERI MISAWA Tsuyoshi U-Nagoya TAKEDA Toshikazu U-Osaka YAMAMOTO Toshihisa U-Osaka FUJIWARA Daisuke U-Tohoku IWASAKI Tomohiko U-Tohoku KIM Young-Jin KAERI Republic of Korea KLOOSTERMAN Jan Leen Petten The Netherlands TSIBOULIA Anatoli IPPE-Obninsk Russian Federation PARATTE Jean-Marie PSI Switzerland CROSSLEY Steve BNFL United Kingdom HESKETH Kevin BNFL BLOMQUIST Roger N. ANL USA GRIMM Karl ANL HILL Robert N. ANL 8 EXECUTIVE SUMMARY The recycling of plutonium in LWRs has for quite some time been seen as an important interim step prior to the large scale introduction of fast reactors; several countries have, in fact, been using MOX fuel in PWRs on a commercial scale for many years. Now that fast reactors are no longer expected to be introduced for some time, the need to manage existing plutonium stocks puts even more emphasis on LWR MOX. Even though there is sufficient experience of MOX in PWRs to be assured of satisfactory performance under existing conditions, the situation is not static and it is very important to address future requirements. There are two main trends which need to be accounted for. First, discharge burn-ups are still increasing steadily. Second, the fissile quality of the plutonium is generally becoming poorer. The decline in fissile quality is partly a consequence of the higher burn-ups, but another major consideration is the effect of recycling MOX fuel itself. Multiple recycle scenarios cause a significant decline in fissile quality in each recycle generation. One consequence is that the initial plutonium content of MOX fuel is considerably increased in each recycle generation and this poses a considerable challenge to current nuclear design codes and the associated nuclear data libraries. The OECD Working Group on the Physics of Plutonium Recycling (WPPR) has considered the issue of multiple recycle of MOX in PWRs in Volumes I and II of its report published in 1995. The main effort was directed towards an international benchmark exercise in which participants were invited to submit solutions to a fully defined problem representative of a multiple recycle scenario in a PWR. Such benchmark exercises are a valuable first step towards understanding the problems to be overcome before a future scenario can be realised in practice. They cannot, of course, identify the correct answer; this must wait until there is experimental or operational experience to learn from. However they can highlight the areas in which current calculational methods and nuclear data start to breakdown and thereby provide a rational basis for directing the research effort. The earlier benchmark work identified major discrepancies between the various nuclear design codes and nuclear data libraries, specifically differences of up to 4%∆k in reactivities. A portion of the range of discrepancy was explained because some of the codes did not apply self-shielding to the resonance treatment of the higher plutonium isotopes; with the large concentration of 242Pu specified in the benchmark, self-shielding in this nuclide was very important. Nevertheless the remaining discrepancy was considered sufficiently large that further work would clearly be necessary before the multiple recycle scenario envisaged in the specification could be implemented. A shortcoming of the initial benchmark was that the cases considered only included one corresponding to today’s situation (with plutonium of good isotopic quality), to one which might arise after many generations of MOX recycle (with extremely poor isotopic quality). Analysis of the intermediate steps was missing, and therefore there was no possibility of determining precisely where the nuclear codes and data libraries would start to lose their applicability. Accordingly, CEA suggested a benchmark in which five consecutive generations of multiple recycle in a PWR would be followed. In the specification of the benchmark, attempts were made to make it as realistic a 9

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