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The scientific feasibility of plutonium management and waste transmutation have been established for the different cases [2,6]: • With homogeneous recycling of Pu and MA in the EPR reactors (Case 1), in the case of the homogeneous multirecycling with a 235 U enriched fuel (MIX) and in the EFR reactors (Case 2) that allow additional transmutation of LLFP in moderated targets. • In the EPR – EFR park (Case 3) with homogeneous recycling of Pu and Np, and transmutation of Am and Cm in targets placed in a moderated neutron spectrum in the fast core. • In the double component hypothesis (Case 4), around 20% of dedicated systems are needed to ensure Pu and MA consumption. • In the double strata (Case 5), around 50% of the first stratum are EFR reactors burning Pu, 5% of dedicated systems assuming MA transmutation. In terms of reduction of the radio toxicity of the ultimate waste in the case of ingestion, the results are roughly of the same order for the different scenarios, depending on the elements considered, with a reduction factor of 3 to 10 for Pu consumption alone, and a reduction factor of 100 for Pu and Minor Actinides management, by comparison to the open cycle (reduction factor of one). Nevertheless, the scenarios are not equivalent if one considers the amount of recycled masses, Scenario 1 leading for example to large amounts of Pu and MA and especially of curium which have to be taken into account when considering the technical feasibility and especially the impact on the cycle. These results lead to consider the development of MA fuels for PWR (with multi-recycling of Pu), for fast reactors (with either mono-recycling of MA and LLFP in moderated targets or multirecycling in quasi standard fuels) and also for dedicated reactors. The R&D programme is presented below according to these three items, after a review of the available results. 4. R&D programme on materials for transmutation The aim of the R&D programme is to obtain elements of technical feasibility for the fuels to be used in the different strategies to contribute to the evaluation of the scenarios in 2006. Aside the homogeneous recycling (in PWR and FR) which requires standard fuels with a low content in minor actinides, the heterogeneous recycling (in FR and ADS) leads to consider fuel with a high content of minor actinides but without uranium to prevent the formation of “new” actinides. This type of fuels can be either solid solutions of actinides or composite fuels with an actinide compound in a matrix support that must be as inert as possible towards neutrons to be stable under irradiation and able to reach very high fission rates up to 90%, far above the standard ones (see Table 2). 462
Table 2. Objectives for transmutation in fast neutron spectrum Targets Standard fuel in FR Composition Inert matrix ~1-7g.cm -3 MA (U, Pu)O 2 Fast fluence (n.m -2 ) 10-40 10 26 (moderated or fast 20 10 26 spectrum) Linear power (W/cm) Min.: 10, max: 400 400 Temperature range 500-2 000 2 200 Fission rate (%) 30% ->>90% 17.5% Prod. helium 36 (FR = 85%, AM~1g/cm 3 ) 0.15 (cm 3 .g -1 of fissile phase) Prod. fission gases 20.6 (FR = 85%, AM~1g/cm 3 ) 3.6 (cm 3 .g -1 of fissile phase) Dose on the cladding in dpa 200 150 For these U free fuels, that represent a technological discontinuity with regards to U and Pu oxides, development is needed in different areas, first with the characterisation of the basic properties of the fuels components, and for the elaboration of the fabrication process, then with the realisation of experimental irradiations and post irradiation examinations to obtain elements of the behaviour under irradiation and also in term of simulation to prospect the behaviour of new concepts. As the different phases require the use of shielded nuclear installations, the time needed to define a solution usable for the industrial level, will be around 15 years and more. For the specific case of fast neutron reactors, a first step will be reached before 2010 with the identification of the performance potential of the tested solutions. This will allow the definition of a second step for 5 to 10 years to reach the ultimate objectives fixed to the selected concepts. This leads to privileged generic and basic research and, along with the present experimental programme, to develop the simulation of irradiated elements and fuels (including specific irradiation tools) and to share this development in international collaborations. The programme detailed below covers a large fields of applications and is presented according to the technology considered with in first, the hypothesis of transmutation in PWR for which the R&D is to be connected to the projects under consideration to burn plutonium, and in second the actions linked to the use of fast neutrons reactors which offer determinate advantages for a transmutation strategy (ratios of fission to capture more favourable than in thermal flux, availability of neutrons) and have proven their capacity to use plutonium. Before the presentation of the experimental programme in FR, a status of the knowledge of the behaviour of the composite fuels is made, to point out the fields of research. In third the research for the fuels to be used in ADS is starting with work beginning on the characterisation of the elements of interest. 5. Fuels studies for transmutation in pressurised reactors The solution considered in the calculations is the homogeneous mode on the basis of the MIX fuel [4], with a fuel composition of 2.7% plutonium, 0.3% americium, 0.4% curium and a uranium enrichment of 4.5%, in a standard UO 2 EPR fuel rod geometry. 463
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Nuclear Development ACTINIDE AND FI
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FOREWORD The objective of the OECD/
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TABLE OF CONTENTS Foreword ........
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EXECUTIVE SUMMARY More than 160 par
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identified. In the fuel area, labor
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17:20-19:05 Session III: Partitioni
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Poster sessions Poster session: Par
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WELCOME ADDRESS Lucila Izquierdo Ge
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WELCOME ADDRESS Michel Hugon Co-ord
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WELCOME ADDRESS Philippe Savelli De
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developments. This will surely beco
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use of FBRs for transmutation toget
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view, i.e. better use of uranium an
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W. Forsberg proposes to reduce the
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1. From the open fuel cycle to the
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Figures 2 and 3 show the radiotoxic
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Denoting the transuranic (TRU) or m
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or, in terms of the fuel burn-up an
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quantities of LWR-MOX and FR-MOX wi
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view of the historic development, t
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Table 5. Assumptions for transmutat
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separating troublesome fission prod
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REFERENCES [1] L.H. Baetslé, Ch. D
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SESSION III Partitioning Chairs: J.
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OVERVIEW OF THE HYDROMETALLURGICAL
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2.1.3 Consequences Owing to the fac
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The extraction and separation mecha
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extractant was observed. As a conse
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2.3.2 Examples of strategies and
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3. Conclusions and perspectives 3.1
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SESSION IV Basic Physics, Materials
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TRANSMUTATION: A DECADE OF REVIVAL
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2.1 The IFR concept and the homogen
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2.3 Dedicated systems Making again
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compound “macro-dispersed” in M
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Figure 3. Sketch of ADS, liquid met
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3.3.2.1 The MEGAPIE project [40] ME
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3.3.2.2 The MUSE experiments The MU
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Figure 8. Comparison of the neutron
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Figure 9. Scenarios at equilibrium
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goals in this field. Since once-thr
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• The use of Thorium in PWRs alwa
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• Understanding of the role of AD
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[17] Y. Arai, T. Ogawa, Research on
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SESSION V Transmutation Systems and
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1. Introduction The term ADS compre
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• Safety should be “designed in
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3. Minor actinide and/or transurani
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Table 2. Values of Dj (neutron cons
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Table 4. Delayed neutron fraction I
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Figure 4. η (Neutrons released per
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Table 5. ADS Distinguishing feature
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While a favourable ADS safety featu
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Optimised mixes of MA and Pu can be
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Moreover, the fuel is where neutron
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REFERENCES [1] L. Van den Durpel et
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[19] D.C. Wade and E. Fujita, Trend
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POSTER SESSION Basic Physics: Nucle
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To conclude, this poster session in
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Five other papers related to ADS co
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SESSION I OVERVIEW OF NATIONAL AND
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1. Current activities for radioacti
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3.2 Results to date and analyses of
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3.2.5.2 JNC JNC is considering the
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4.6 Short-term increase in radiatio
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Annex 1 R&D scheme for partitioning
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Annex 3 Members of the Advisory Com
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plutonium can be recycled in pressu
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choices and the implementation of m
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1. Introduction Since the 5th Infor
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strata” approach which would invo
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IAEA ACTIVITIES IN THE AREA OF EMER
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actually started to do so) because
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establishment of an international R
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The accelerator driven transmutatio
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substantiate this recommendation, s
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current, advanced and innovative nu
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ACCELERATOR DRIVEN SUB-CRITICAL SYS
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demonstration of feasibility of a E
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An extended “skeleton” for ADS
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• Fertile support (uranium) is no
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7. Conclusions The TWG under the ch
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1. Introduction The priorities for
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In the EURATOM Fourth Framework Pro
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Table 2. Cluster on transmutation-t
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6. Community research for the perio
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REFERENCES [1] “Council Decision
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1. Introduction Back in 1989, the O
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would need the continuation of tech
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individual isotopes as a function o
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Therefore, while there is continuin
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[9] OECD/NEA, Overview of Physics A
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RECENT TOPICS IN R&D FOR THE OMEGA
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Figure 1. Partitioning and transmut
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The present 4-GPP necessitates a pr
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5. Concluding remarks In 1999, the
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REFERENCES [1] T. Mukaiyama, T. Tak
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1. Introduction CIEMAT is actively
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adiotoxicity to be managed could al
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Figure 3. Mass composition of the d
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Figure 6. Fuel cycle assumed in the
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the 4 batches scheme, allowing to a
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Figure 11. Transmutation efficiency
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1. Introduction Spent fuels of mode
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Figure 3. A change in radiotoxicity
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These dependencies are shown on Fig
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When increasing the moderator fract
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Even greater power increases are ob
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The effect of a moderator volume fr
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Table 11. Different isotopes contri
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Thus the transmutation of such FPs
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ASSESSMENT OF NUCLEAR POWER SCENARI
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elease probabilities. The time dist
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Table 2. Annual heavy nuclide contr
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Figure 3. Reduction of potential ra
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DISPOSAL OF PARTITIONING-TRANSMUTAT
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Figure 2. Decay heat from SNF 2000
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Figure 3. Shorter-lived HHR reposit
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4. Management of low-heat, long-liv
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isotope from other caesium isotopes
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THE AMSTER CONCEPT J. Vergnes 1 , D
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Figure 1. Layout diagram of the mol
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Table 1. Definition of configuratio
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We therefore adopted a partial purg
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conceivable. Thus by increasing the
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6. R&D needed to validate the AMSTE
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SESSION III PARTITIONING J.P. Glatz
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PARTITIONING-SEPARATION OF METAL IO
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The terpyridyl reagent (ligand L 1
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Figure 2. The synthesis of ADTPTZ a
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2.4 Implications for partitioning T
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SEPARATION OF MINOR ACTINIDES FROM
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installed in a hot cell. The feed w
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the concentrations of U, Pu and Np
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Table 2 shows the recovery in the r
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PARTITIONING ANIONIC AGENTS BASED O
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which of these, the Co 3+ , Fe 3+ a
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This dianionic species must be extr
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Figure 6 Ph 2 P acetone PPh 2 H2 O
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Figure 9 H 3 C RO(CH 2 )n CH 3 (CH
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[7] J. Rais and P. Selucky, Nucleon
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PYROCHEMICAL PROCESSING OF IRRADIAT
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The metallic cadmium product of the
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Figure 2. Schematic flow-sheet for
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R&D OF PYROCHEMICAL PARTITIONING IN
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(first of all pumps) for fluoride m
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4. Research on material and equipme
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REFERENCES [1] Uhlir J., Pyrochemic
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1. Introduction The increasing inte
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Figure 2. Stainless steel box with
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Figure 4. U deposit on solid cathod
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Figure 7. Schematic flow of the cou
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actinide elements from spent (metal
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DEVELOPMENT OF PLUTONIUM RECOVERY P
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uranium dendrite and that uranium c
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Table 1. Conditions and results of
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Cathode potential went down to -1.6
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Figure 6. Change of LCC potential i
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Figure 9. Relation between Pu conce
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consideration described in the prec
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[13] Y. Arai, S. Fukushima, K. Shio
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SESSION IV BASIC PHYSICS, MATERIALS
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1. Introduction The reduction of th
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agrees ours within limits of errors
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Figure 1. Thermal neutron capture c
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[18] A.P. Baerg, R.M. Bartholomew,
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1. Introduction Nowadays it is well
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In order to describe the inter-nucl
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kind of measurements allow to chara
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Figure 6. Two-dimensional cluster p
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Figure 8. Excitation functions for
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REFERENCES [1] D. Ridikas, thesis,
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1. Introduction Since 1991, the Com
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Experimental reactivity control tec
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Table 2. Neutron intensities Target
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experimental channels (horizontal a
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376
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Table 3. Planned experimental progr
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1. Introduction and benchmark speci
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neutrons. Since the neutron flux is
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Figure 2. Microscopic capture cross
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Figure 4. k eff variation in the st
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2.4 Neutron flux distribution One r
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etween the highest and the lowest v
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The isotope specific β eff values
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SESSION IV BASIC PHYSICS, MATERIALS
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1. Introduction Due to its excellen
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Figure 2. Tests scheme 0 340 h. 1 0
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Figure 4. Auger depth profile conce
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Figure 8. Auger depth profile conce
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deposited at the cold zone, and the
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inner layer grows inward from the o
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[8] V.M. Fedirko, O.I. Eliseeva, V.
Page 412 and 413: 1. Introduction One of the main par
Page 414 and 415: 3. Tantalum target irradiation The
Page 416 and 417: At 10-MeV neutron irradiation, radi
Page 418 and 419: 1. Introduction HYPER (HYbrid Power
Page 420 and 421: this study, we used an orthogonal c
Page 422 and 423: Figure 5. Temperature distribution
Page 424 and 425: Figure 7. Thermal stress distributi
Page 427 and 428: FUEL/TARGET CONCEPTS FOR TRANSMUTAT
Page 429 and 430: (U 0.55 Pu 0.4 Np 0.05 )O 2 fuels w
Page 431 and 432: Figure 3. Left: Ceramograph of a (Z
Page 433 and 434: Figure 6. Left: ceramograph of a(Zr
Page 435 and 436: AMERICIUM TARGETS IN FAST REACTORS
Page 437 and 438: The reference case for all comparis
Page 439 and 440: It should be underlined that this c
Page 441 and 442: Cases Table 3. Heterogeneous recycl
Page 443 and 444: • A later step could be to add Cm
Page 445 and 446: RESEARCH ON NITRIDE FUEL AND PYROCH
Page 447 and 448: temperature for (Cm,Pu)N followed t
Page 449 and 450: Figure 1. Temperature dependence of
Page 451 and 452: The difference of two fuel pins exi
Page 453 and 454: In addition to the voltammetric stu
Page 455 and 456: 2 wt% of Pu at 773 K. For the momen
Page 457: [13] M. Akabori, M. Takano, A. Itoh
Page 460 and 461: 1. Introduction For the management
Page 464 and 465: Another option using a basis of sta
Page 466 and 467: 6.2.1 Inert matrices 6.2.1.1 MgAl 2
Page 468 and 469: eached respectively 38.5% and 70% F
Page 470 and 471: Figure 4. Experiments for MA transm
Page 472 and 473: Figure 5a. Ecrix B rig Figure 5b. E
Page 474 and 475: A CEA/Minatom work programme is und
Page 476 and 477: 9.3 Programme for dedicated fuels F
Page 478 and 479: [14] R.J.M. Konings et al., The EFT
Page 480 and 481: 1. Introduction An accelerator driv
Page 482 and 483: corresponding Pb-Bi velocity is 1.1
Page 484 and 485: the fission product target. The rod
Page 486 and 487: fuel rods are at the TRU assembly t
Page 489: SESSION V TRANSMUTATION SYSTEMS AND
Page 492 and 493: 1. Introduction Since the 50s, nitr
Page 494 and 495: A three dimensional model of a sub-
Page 496 and 497: Figure 4. Change in k-eigenvalue fo
Page 498 and 499: [4] Y. Arai et al., Experimental Re
Page 500 and 501: Nomenclature ADS: ATW: GT-MHR: LOF:
Page 502 and 503: Regarding switching off the beam, o
Page 504 and 505: Figure 3. Beam blocking 10 min (200
Page 506 and 507: Figure 7. A possible scenario for n
Page 508 and 509: [15] Greenspan E. et al., The Encap
Page 510 and 511: 1. Introduction In the EADF design
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Equation (6) can be improved by con
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where L is obtained by a summation
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Figure 1. The natural convection im
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Figure 4 shows the temperature tren
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[12] P.H. Wakker, Thermal Hydraulic
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1. Introduction Research and develo
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Table 2. Core design parameters for
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2.2 Representation of MA transmutat
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Figure 1(b) shows the cases for the
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It is found that the higher MA tran
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REFERENCES [1] T. Ikegami, H. Hayas
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1. Introduction The management of t
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Table 1. Core performance of MA and
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Figure 3. Nuclear electricity capac
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Table 3. Experimental items at PEF
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REFERENCES [1] Takano H., Akie H.,
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1. Introduction and background The
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neutron source, the reactor can mai
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atoms. For fuel region Rf = 2.5 cm,
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Figure 3. Neutron flux spectra for
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A possible way to maintain the k ef
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higher than 99% of 239 Pu, and high
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TRANSMUTATION OF NUCLEAR WASTES WIT
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Figure 1. PBT conceptual view Table
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very tight holders for fission frag
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5. Cooling system A preliminary des
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spectral densities [10,11] and can
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MYRRHA, A MULTI-PURPOSE ADS FOR R&D
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hexagonal assemblies of 122 mm plat
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to achieve the requested performanc
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3 MYRRHA associated R&D programme F
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collaboration with Forschungszentru
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• Industrial partners, in particu
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1. Introduction The transmutation o
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Existing accelerators have been des
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suggested to look for an innovative
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Table 1. Main lead-bismuth eutectic
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4.3 The core The basic fuel sub-ass
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Figure 1. Experimental accelerator
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HELIUM-COOLED REACTOR TECHNOLOGIES
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of its potential use in nuclear wea
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Figure 2. Neutron flux distribution
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atio. Given this rate of destructio
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Figure 5. Irradiated TRISO particle
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in ceramic-coated microspheres of t
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(LOCA) event. The effect on this fe
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Figure 13. Elevation AD-FMHR The fa
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Deep burn-up of 239 Pu and fissiona
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POSTER SESSION PARTITIONING M.J. Hu
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1. Introduction The study of the be
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Plutonium was simulated with the no
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The influence of uranium and pluton
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The influence of uranium and pluton
Page 624 and 625:
REFERENCES [1] I.I. Nazarenko, A.M.
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1. Introduction The long-term radio
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Ce Ce 3+ Cl - Cl 2 The voltammogram
Page 630 and 631:
Figure 3. Chronopotentiograms for t
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Figure 4. Potentiometric titrations
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Experimental solubilization tests w
Page 636 and 637:
[13] H. Flood T. Förland and K. Mo
Page 638 and 639:
1. Introduction The separation of l
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Figure 4. Synthesis of amides 11-15
Page 642 and 643:
1. Introduction Over the recent yea
Page 644 and 645:
2.3.2 Set-up We set up a single HFM
Page 646 and 647:
lower flow rates, Am(III) would be
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THE POTENTIAL OF NANO- AND MICROPAR
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efficiently and stable. This can be
Page 653 and 654:
Figure 1a. Zetapotential of NTA-mod
Page 655 and 656:
Scheme 7. Magnetic silica particles
Page 657:
[13] L.H. Delmau, N. Simon, M.J. Sc
Page 660 and 661:
1. Introduction 137 90 Extraction p
Page 662 and 663:
Figure 3. Schematic drawing of the
Page 664 and 665:
(24), 8-PhPO(OH)-O-COSAN (25), and
Page 666 and 667:
REFERENCES [1] Kyrš M., +H PiQHN S
Page 668 and 669:
1. Introduction A heavy-water CANDU
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These data show that fuel lifetime
Page 673 and 674:
RECENT PROGRESSES ON PARTITIONING S
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hot tests (See Table2) was enough f
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trace amount of Am and Eu. The HBTM
Page 679 and 680:
6. Conclusion Declassification of t
Page 681:
POSTER SESSION BASIC PHYSICS: NUCLE
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1. Introduction Among the large num
Page 686 and 687:
The simulation of the spallation pr
Page 688 and 689:
Table 1. Parameters of the two coll
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Figure 4. Radial distribution of th
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6. The neutron escape line The comm
Page 694 and 695:
Figure 7. Neutron background at the
Page 697 and 698:
RECENT CAPTURE CROSS-SECTIONS VALID
Page 699 and 700:
Figure 1. The GENEPI accelerator an
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2.3.3 Neutron flux measurements •
Page 703 and 704:
Figure 6. Time spectrum of 3 He gas
Page 705 and 706:
4. Analysis 4.1 Background subtract
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Figure 11. ENDF/B-VI, JEF2.2 and JE
Page 709 and 710:
DOUBLE DIFFERENTIAL CROSS-SECTION F
Page 711 and 712:
3. Conclusion Double differential c
Page 713 and 714:
Figure 3. Preliminary results of do
Page 715 and 716:
MEASUREMENTS OF PARTICULE EMISSION
Page 717 and 718:
2. Experimental set-up The experime
Page 719:
4. Results Figure 3 presents neutro
Page 722 and 723:
1. Introduction Intermediate-energy
Page 724 and 725:
Table 1. Relative neutron-induced c
Page 726 and 727:
elow about 70 MeV [24] , where σ n
Page 728 and 729:
Since for sub-actinides Γ f /Γ n
Page 730 and 731:
[10] V.P. Eismont, A.V. Prokofiev,
Page 733 and 734:
NUCLEON-INDUCED FISSION CROSS-SECTI
Page 735 and 736:
Figure 1. Scheme of the new code Z
Page 737 and 738:
Figure 3. Neutron-induced fission c
Page 739:
REFERENCES [1] J. Raynal, Proceedin
Page 742 and 743:
1. Introduction During the past few
Page 744 and 745:
(same surface and 0.5 mm thickness)
Page 746 and 747:
Figure 2. Dependence of the total a
Page 748 and 749:
Figure 3. Neutron radiative capture
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[8] MCNP, A General Monte Carlo Cod
Page 752 and 753:
1. Introduction New reactors using
Page 754 and 755:
Figure 1. Excited states of 209 Bi
Page 756 and 757:
Figure 3. The fission probability o
Page 759 and 760:
MEASUREMENT OF DOUBLE DIFFERENTIAL
Page 761 and 762:
Figure 1. Global view of the experi
Page 763 and 764:
To get the proton (deuteron) energy
Page 765 and 766:
3.1 Corrections Several corrections
Page 767 and 768:
Figure 11. Active target fraction (
Page 769 and 770:
d 2 σ Figure 14. Proton for n + Pb
Page 771 and 772:
HIGH AND INTERMEDIATE ENERGY NUCLEA
Page 773 and 774:
eactions, since the pre-equilibrium
Page 775 and 776:
calculate the very short-lived radi
Page 777 and 778:
cross-sections; the secondary react
Page 779 and 780:
All possible nuclear reactions will
Page 781 and 782:
A STUDY ON BURNABLE ABSORBER FOR A
Page 783 and 784:
2. Burnable absorber for HYPER 2.1
Page 785 and 786:
Table 2. One-group effective cross-
Page 787 and 788:
of the core, is directly determined
Page 789 and 790:
Figure 4. Required proton beam curr
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Figure 8. 10 B depletion in HYPER-H
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POSTER SESSION TRANSMUTATION SYSTEM
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1. Introduction In the framework of
Page 798 and 799:
Φ >1 MeV = 1.0 10 13 to 1.0 x 10 1
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3. Irradiation targets and irradiat
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e transmuted in BR2 hence remain va
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Table 6. Atom percent concentration
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advantage, with respect to FRs, of
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ENHANCEMENT OF ACTINIDE INCINERATIO
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Here Σ fC , ( E) are the fission a
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pellet and the steel cladding. In o
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Table 3.Neutronics parameters of hy
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Figure 3. Neutron spectra averaged
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containing FA with B 4 C cladding i
Page 821:
REFERENCES [1] ANSALDO Technical Re
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1. Introduction At present, there a
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target means a change in k and the
Page 828 and 829:
Following the normal procedure for
Page 830 and 831:
Acknowledgements This study has bee
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1. ADS description A conceptual des
Page 834 and 835:
Substitution of (9) into (8), and u
Page 836 and 837:
With the coupling LAHET + MCNP-DSP,
Page 838 and 839:
Figure 3. Comparison for 1 and 5 pu
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MOLTEN SALTS AS POSSIBLE FUEL FLUID
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2. The fuel salt for MSB concept Ma
Page 845 and 846:
and minor actinides must be removed
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4. Container material studies 4.1 F
Page 849 and 850:
management. The major developments
Page 851:
REFERENCES [1] H.J. MacPherson, Dev
Page 854 and 855:
1. Introduction The Energy Amplifie
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Table 1. Main parameters of the EAD
Page 858 and 859:
Table 5. Neutron balance in the who
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Table 7. Neutron flux distributions
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Table 8. Displacement rates DPA/yea
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DEEP UNDERGROUND TRANSMUTOR (PASSIV
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passive state. By operating at a hi
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I have proposed using an accelerato
Page 871 and 872:
Figure 1. Layout of deep undergroun
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RADIATION CHARACTERISTICS OF PWR MO
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Table 1. Radiotoxicity of actinides
Page 877 and 878:
RADIATION CHARACTERISTICS OF URANIU
Page 879 and 880:
Table 1. Radiotoxicity of actinides
Page 881 and 882:
INTERNATIONAL CO-OPERATION ON CREAT
Page 883 and 884:
an international base to combine ef
Page 885:
• Second topic: interaction of pr
Page 888 and 889:
1. Introduction The role of acceler
Page 890 and 891:
MEPI within the framework of Projec
Page 893 and 894:
NEW ORIGINAL IDEAS ON ACCELERATOR D
Page 895 and 896:
During conceptual investigations of
Page 897 and 898:
delay, interface and computer. The
Page 899 and 900:
2. Channel-vessel design of ADS bla
Page 901 and 902:
Table 1. Characteristics of the ful
Page 903:
[14] Karavaev G.N., Kiselev G.V., M
Page 906 and 907:
1. Introduction The problem of nucl
Page 908 and 909:
Table 3. Radiotoxicity in americium
Page 910 and 911:
Table 5. Characteristics of station
Page 912 and 913:
1. Introduction The atomic power en
Page 914 and 915:
of lead-bismuth target are given in
Page 917 and 918:
CRITICAL AND SUB-CRITICAL GT-MHRs F
Page 919 and 920:
Table 1. Basic GT-MHR reactor param
Page 921 and 922:
Figure 2. Typical change of the ave
Page 923 and 924:
Scenario S4. This case is actually
Page 925 and 926:
Figure 3. A change in radiotoxicity
Page 927:
[13] P. Goberis, Modelling of Innov
Page 930 and 931:
1. Introduction The Nuclear Enginee
Page 932 and 933:
Some simplifications have been made
Page 934 and 935:
Figure 3. Velocity vectors Some of
Page 936 and 937:
Figure 6. Temperature evolution at
Page 938 and 939:
• Two main reasons can explain th
Page 940 and 941:
1. Introduction Actually, we notice
Page 942 and 943:
This problem can be solved by using
Page 944 and 945:
The evaluations obtained in [2] hav
Page 946 and 947:
REFERENCES [1] Management and Dispo
Page 948 and 949:
1. Background Radiation background
Page 950 and 951:
the long-term hazard of spent fuel,
Page 952 and 953:
In a transmutation fuel cycle inclu
Page 954 and 955:
Figure 4. Potential biological haza
Page 956 and 957:
cooling prior to SF reprocessing an
Page 958:
REFERENCES [1] White Book of Nuclea
Page 961 and 962:
ORDER FORM OECD Nuclear Energy Agen
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