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1. Introduction <strong>Nuclear</strong> waste, especially spent fuel from nuclear reactors containing long-lived radionuclides represented mainly by actinides and long-lived fission products, presents a common problem for all countries operating nuclear power plants. Satisfactory solution of this problem is a factor limiting to a considerable extent the further nuclear power industry development, namely in developed countries. The present technical and technological sum of knowledge indicates that this problem could be largely resolved by using the transmutation technology so that the nuclear power industry may become widely acceptable for the public. The use of transmutation reactors with fluoride salts based liquid fuel might be one of the possible answers. In the near future, these systems might be conceived as critical ones and successively as sub-critical accelerator driven reactor systems. In addition to the nuclear burning of plutonium and minor actinides produced in the U-Pu cycle these reactor systems might consecutively operate within the U-Th cycle as well. The advantage of the molten salt transmutation reactors (MSTR) demonstrates itself above all in connection with a continuous or at least quasi-continuous chemical separation process. For such a compact coupling of MSTR with chemical reprocessing it will be very appropriate to keep fuel in one chemical form, as far as possible, in the course of the entire fuel cycle. Accordingly, if the MSTR fuel will be based on fluoride melt then the separation processes should also be based on separation techniques from fluoride melt media. Pyrochemical and pyrometallurgical technologies comply generally with this requirement [1]. 2. Czech research and development programme The Czech research and development programme in the field of pyrochemical and pyrometallurgical separation is based first of all on the experience acquired in the past in the development and realisation of a pilot-plant fluoride technology for the reprocessing of spent fuel from the Russian BOR-60 fast reactor [2]. At present, this experience is utilised for the development of suitable separation processes and technologies for the fluoride based MSTR fuel cycle. Experimental and theoretical studies in the field of pyrochemical technology development for the MSTR fuel cycle are oriented in particular to the following areas: • Technological research in the field of the “Fluoride volatility” method directed at the suitability verification of a technology for thermal or fast reactor spent fuel reprocessing, which may result in a product the form and composition of which might be applicable as a starting material for the production of liquid fluoride fuel for MSTR. Consequently, the objective is a separation of a maximum fraction of uranium component from Pu, minor actinides and fission products. Integral part of this research also is the flowsheeting research – working out a proposal for a suitable technological flowsheet for treating spent fuel into a form fitted for MSTR including the separation procedures before transmutation (front-end) and separation processes after passage of fuel through the transmutor (back-end). • Research on material and equipment for fluoride salts media connected with the experimental programme on ADETTE technological loops. Objective of the programme is verification of the new developed construction material for fluoride melts, development of selected devices 308
(first of all pumps) for fluoride melts and acquirement of practice in fluoride melts handling and manipulation in greater amounts. • Laboratory research on electro-separation methods in fluoride melts media in relation to the study of their properties. The effort in this field is aimed first of all to the determination of optimum conditions for uranium and fission product separations and to the selection of suitable electrolyte composition based on fluoride salt mixture. At present, the greatest attention is aimed to the realisation of the pilot-plant technology for the separation of the uranium component from other spent fuels components by the modified “Fluoride volatility” method. The other two areas mentioned are also intensively studied. 3. Technological research in the area of “fluoride volatility” method Technological research of the “fluoride volatility” method can be ranked into the “front-end” area within the MSTR fuel cycle. It is a separation process for reprocessing spent fuel from thermal or fast reactors into a form suitable for the MSTR. The main operations of this process are: • Removal of the cladding material from spent fuel. • Conversion of the fuel into a powder form (oxides) of a granulometric composition suitable for the fluorination reaction. • Fluorination of the fuel (the purpose of this operation is the separation of the uranium component from plutonium, minor actinides and most of fission products). • Uranium component purification. The essential research activities are centred upon the technological verification of items 3 and 4 leading to the removal of the main portion of the uranium component from spent fuel. The proposed technology is based on the spent fuel fluorination with gaseous fluorine in a flame fluorination reactor, where the volatile fluorides are separated from the non-volatile ones, and on the subsequent purification of the component by using technological operations of condensation and distillation and also of sorption. As the fluorination reaction is suggested as a flame reaction, the necessary size of the flame fluorination reactor (Figure 1) is a critical parameter influencing dimensions of the entire experimental technological line. According to the process design, up to 95-99% of uranium in the form of volatile UF 6 will be removed from the non-volatile fluorides of plutonium (PuF 4 ), minor actinides and majority of fission products. In this way, the component representing the greatest share of the spent fuel will be removed. The technological research is closely associated with the “flowsheeting research”, the aim of which is also to act as an unifying framework of the individual research activities, in addition to the working out of the technological flowsheet. In Figure 2 a simplified flowsheet is presented of the designed MSTR fuel cycle, the “front-end” of which is based on the “Fluoride volatility” method. 309
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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
Page 257 and 258: Figure 1. Layout diagram of the mol
Page 259 and 260: Table 1. Definition of configuratio
Page 261 and 262: We therefore adopted a partial purg
Page 263 and 264: conceivable. Thus by increasing the
Page 265 and 266: 6. R&D needed to validate the AMSTE
Page 267: SESSION III PARTITIONING J.P. Glatz
Page 271 and 272: PARTITIONING-SEPARATION OF METAL IO
Page 273 and 274: The terpyridyl reagent (ligand L 1
Page 275 and 276: Figure 2. The synthesis of ADTPTZ a
Page 277 and 278: 2.4 Implications for partitioning T
Page 279 and 280: SEPARATION OF MINOR ACTINIDES FROM
Page 281 and 282: installed in a hot cell. The feed w
Page 283 and 284: the concentrations of U, Pu and Np
Page 285 and 286: Table 2 shows the recovery in the r
Page 287 and 288: PARTITIONING ANIONIC AGENTS BASED O
Page 289 and 290: which of these, the Co 3+ , Fe 3+ a
Page 291 and 292: This dianionic species must be extr
Page 293 and 294: Figure 6 Ph 2 P acetone PPh 2 H2 O
Page 295 and 296: Figure 9 H 3 C RO(CH 2 )n CH 3 (CH
Page 297: [7] J. Rais and P. Selucky, Nucleon
Page 301 and 302: PYROCHEMICAL PROCESSING OF IRRADIAT
Page 303 and 304: The metallic cadmium product of the
Page 305 and 306: Figure 2. Schematic flow-sheet for
Page 307: R&D OF PYROCHEMICAL PARTITIONING IN
Page 311 and 312: 4. Research on material and equipme
Page 313: REFERENCES [1] Uhlir J., Pyrochemic
Page 316 and 317: 1. Introduction The increasing inte
Page 318 and 319: Figure 2. Stainless steel box with
Page 320 and 321: Figure 4. U deposit on solid cathod
Page 322 and 323: Figure 7. Schematic flow of the cou
Page 324 and 325: actinide elements from spent (metal
Page 327 and 328: DEVELOPMENT OF PLUTONIUM RECOVERY P
Page 329 and 330: uranium dendrite and that uranium c
Page 331 and 332: Table 1. Conditions and results of
Page 333 and 334: Cathode potential went down to -1.6
Page 335 and 336: Figure 6. Change of LCC potential i
Page 337 and 338: Figure 9. Relation between Pu conce
Page 339 and 340: consideration described in the prec
Page 341: [13] Y. Arai, S. Fukushima, K. Shio
Page 345: SESSION IV BASIC PHYSICS, MATERIALS
Page 348 and 349: 1. Introduction The reduction of th
Page 350 and 351: agrees ours within limits of errors
Page 352 and 353: Figure 1. Thermal neutron capture c
Page 354 and 355: [18] A.P. Baerg, R.M. Bartholomew,
Page 356 and 357: 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.
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1. Introduction One of the main par
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3. Tantalum target irradiation The
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At 10-MeV neutron irradiation, radi
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1. Introduction HYPER (HYbrid Power
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this study, we used an orthogonal c
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Figure 5. Temperature distribution
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Figure 7. Thermal stress distributi
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FUEL/TARGET CONCEPTS FOR TRANSMUTAT
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(U 0.55 Pu 0.4 Np 0.05 )O 2 fuels w
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Figure 3. Left: Ceramograph of a (Z
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Figure 6. Left: ceramograph of a(Zr
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AMERICIUM TARGETS IN FAST REACTORS
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The reference case for all comparis
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It should be underlined that this c
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Cases Table 3. Heterogeneous recycl
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• A later step could be to add Cm
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RESEARCH ON NITRIDE FUEL AND PYROCH
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temperature for (Cm,Pu)N followed t
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Figure 1. Temperature dependence of
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The difference of two fuel pins exi
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In addition to the voltammetric stu
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2 wt% of Pu at 773 K. For the momen
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[13] M. Akabori, M. Takano, A. Itoh
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1. Introduction For the management
Page 462 and 463:
The scientific feasibility of pluto
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Another option using a basis of sta
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6.2.1 Inert matrices 6.2.1.1 MgAl 2
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eached respectively 38.5% and 70% F
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Figure 4. Experiments for MA transm
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Figure 5a. Ecrix B rig Figure 5b. E
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A CEA/Minatom work programme is und
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9.3 Programme for dedicated fuels F
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[14] R.J.M. Konings et al., The EFT
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1. Introduction An accelerator driv
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corresponding Pb-Bi velocity is 1.1
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the fission product target. The rod
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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
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[4] Y. Arai et al., Experimental Re
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Nomenclature ADS: ATW: GT-MHR: LOF:
Page 502 and 503:
Regarding switching off the beam, o
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Figure 3. Beam blocking 10 min (200
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Figure 7. A possible scenario for n
Page 508 and 509:
[15] Greenspan E. et al., The Encap
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1. Introduction In the EADF design
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Equation (6) can be improved by con
Page 514 and 515:
where L is obtained by a summation
Page 516 and 517:
Figure 1. The natural convection im
Page 518 and 519:
Figure 4 shows the temperature tren
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[12] P.H. Wakker, Thermal Hydraulic
Page 522 and 523:
1. Introduction Research and develo
Page 524 and 525:
Table 2. Core design parameters for
Page 526 and 527:
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
Page 534 and 535:
1. Introduction The management of t
Page 536 and 537:
Table 1. Core performance of MA and
Page 538 and 539:
Figure 3. Nuclear electricity capac
Page 540 and 541:
Table 3. Experimental items at PEF
Page 542 and 543:
REFERENCES [1] Takano H., Akie H.,
Page 544 and 545:
1. Introduction and background The
Page 546 and 547:
neutron source, the reactor can mai
Page 548 and 549:
atoms. For fuel region Rf = 2.5 cm,
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Figure 3. Neutron flux spectra for
Page 552 and 553:
A possible way to maintain the k ef
Page 554 and 555:
higher than 99% of 239 Pu, and high
Page 557 and 558:
TRANSMUTATION OF NUCLEAR WASTES WIT
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Figure 1. PBT conceptual view Table
Page 561 and 562:
very tight holders for fission frag
Page 563 and 564:
5. Cooling system A preliminary des
Page 565 and 566:
spectral densities [10,11] and can
Page 567 and 568:
MYRRHA, A MULTI-PURPOSE ADS FOR R&D
Page 569 and 570:
hexagonal assemblies of 122 mm plat
Page 571 and 572:
to achieve the requested performanc
Page 573 and 574:
3 MYRRHA associated R&D programme F
Page 575 and 576:
collaboration with Forschungszentru
Page 577:
• Industrial partners, in particu
Page 580 and 581:
1. Introduction The transmutation o
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Existing accelerators have been des
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suggested to look for an innovative
Page 586 and 587:
Table 1. Main lead-bismuth eutectic
Page 588 and 589:
4.3 The core The basic fuel sub-ass
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Figure 1. Experimental accelerator
Page 593 and 594:
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
Page 603 and 604:
in ceramic-coated microspheres of t
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(LOCA) event. The effect on this fe
Page 607 and 608:
Figure 13. Elevation AD-FMHR The fa
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Deep burn-up of 239 Pu and fissiona
Page 613:
POSTER SESSION PARTITIONING M.J. Hu
Page 616 and 617:
1. Introduction The study of the be
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Plutonium was simulated with the no
Page 620 and 621:
The influence of uranium and pluton
Page 622 and 623:
The influence of uranium and pluton
Page 624 and 625:
REFERENCES [1] I.I. Nazarenko, A.M.
Page 626 and 627:
1. Introduction The long-term radio
Page 628 and 629:
Ce Ce 3+ Cl - Cl 2 The voltammogram
Page 630 and 631:
Figure 3. Chronopotentiograms for t
Page 632 and 633:
Figure 4. Potentiometric titrations
Page 634 and 635:
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
Page 640 and 641:
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
Page 649 and 650:
THE POTENTIAL OF NANO- AND MICROPAR
Page 651 and 652:
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
Page 670 and 671:
These data show that fuel lifetime
Page 673 and 674:
RECENT PROGRESSES ON PARTITIONING S
Page 675 and 676:
hot tests (See Table2) was enough f
Page 677 and 678:
trace amount of Am and Eu. The HBTM
Page 679 and 680:
6. Conclusion Declassification of t
Page 681:
POSTER SESSION BASIC PHYSICS: NUCLE
Page 684 and 685:
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
Page 690 and 691:
Figure 4. Radial distribution of th
Page 692 and 693:
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
Page 701 and 702:
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
Page 707 and 708:
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
Page 750 and 751:
[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
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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
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Substitution of (9) into (8), and u
Page 836 and 837:
With the coupling LAHET + MCNP-DSP,
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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
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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
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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
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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
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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
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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
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ORDER FORM OECD Nuclear Energy Agen
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