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1. Introduction Radioactive by-products are unavoidably generated during normal reactor operation. Some of these by-products are very long-lived and radiotoxic elements which must be separated from the biosphere for a very long time. The potential harmfulness of the wastes generated by reprocessing are primarily due to the presence of Minor Actinides (MA) and they are of special concern regarding partitioning and transmutation. Current reprocessing technology is based on the aqueous PUREX process in which uranium and plutonium are recovered. The technique can also be extended for the recovery of neptunium, but americium and curium cannot be separated directly in this process. The partitioning of MA is instead done by advanced reprocessing of High Level Liquid Waste (HLLW) generated by the PUREX process, and different systems based on liquid-liquid extraction have been proposed world-wide. Due to the difficult separation of trivalent MA from trivalent lanthanides (Ln) especially at high acidities, two step processes are at present considered. In the first step, at high acidity, a group separation of MA and lanthanides is carried out, followed by a separation of MA from lanthanides at lower acidity, see Figure 1. Figure 1. Main routes for the separation of MA from HLLW dissolved fuel PUREX 1 cycle process HLLW 2 cycle process Ln / MA separation (at high acidity) FP FP (Ln) MA separation (at high acidity) Ln / MA MA separation (at low acidity) Ln MA MA Transmutation In the French DIAMEX (DIAMide EXtraction) process the minor actinides are directly extracted from the PUREX raffinate together with fission lanthanides using the completely combustible DiMethyl-DiButyl-TetraDecyl MalonAmide (DMDBTDMA). The MA(III)+Ln(III) mixture generated after this first step is low-acidic to facilitate the second process, the SANEX process, which concerns the separation of the MA from the lanthanides. This process is based on the BTP, which belongs to a new family of extractants, the Bis-Triazinyl-Pyridine developed by Z. Kolarik et al, and is very efficient for a selective extraction of MA(III) at high acidity [1] and shows good capabilities in centrifugal extractors. In the present work, the 2,6-Bis(5,6-alkyl-1,2,4-Triazin-3-yl)Pyridine (nPr-BTP) process has been tested in continuous counter-current extraction experiments, using a centrifugal extractor battery 280
installed in a hot cell. The feed was a genuine MA(III)+Ln(III) mixture obtained from small scale PUREX/DIAMEX reprocessing of commercial LWR fuel (45.2 GWd/tM) [2]. 2. Experimental 2.1 Reagents The nPr-BTP compound was obtained from CEA Marcoule [3]. It was dissolved, using an ultrasonic bath, in Hydrogenated TetraPropene (TPH) and 30vol% of octanol obtained from PANCHIM (France) and MERCK (Germany), respectively. The solvent with a final concentration of 0.04M nPr-BTP was directly used as organic phase in the centrifugal extractor experiment. All reagents and chemicals were of the analytical reagent grade. MQ grade water (18 MΩ/ cm) was used for all dilutions. 2.2 Continuous experiments using a genuine MA/Ln fraction The centrifugal extractor equipment installed in the hot cells, see Figure 2, is described elsewhere [4,5]. For the nPr-BTP process, 16 extractors were used, with 5 extraction stages, 3 acid scrubbing stages and 8 strip stages. The continuous counter-current centrifugal extraction scheme is shown in Figure 3. This flow-sheet was optimised on the basis of preliminary data obtained from batch tests with spiked solutions [6]. The genuine MA/Ln solution obtained as a product in the DIAMEX process was used as feed solution and adjusted to 1 M HNO 3 with concentrated nitric acid. Figure 2. Photograph showing the 16 stage continuous counter-current extractor battery installed in the hot cell 281
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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
Page 230 and 231: The effect of a moderator volume fr
Page 232 and 233: Table 11. Different isotopes contri
Page 234 and 235: Thus the transmutation of such FPs
Page 237 and 238: ASSESSMENT OF NUCLEAR POWER SCENARI
Page 239 and 240: elease probabilities. The time dist
Page 241 and 242: Table 2. Annual heavy nuclide contr
Page 243 and 244: Figure 3. Reduction of potential ra
Page 245 and 246: DISPOSAL OF PARTITIONING-TRANSMUTAT
Page 247 and 248: Figure 2. Decay heat from SNF 2000
Page 249 and 250: Figure 3. Shorter-lived HHR reposit
Page 251 and 252: 4. Management of low-heat, long-liv
Page 253 and 254: isotope from other caesium isotopes
Page 255 and 256: 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: SEPARATION OF MINOR ACTINIDES FROM
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 and 308: R&D OF PYROCHEMICAL PARTITIONING IN
Page 309 and 310: (first of all pumps) for fluoride m
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
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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.
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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
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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
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SESSION V TRANSMUTATION SYSTEMS AND
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1. Introduction Since the 50s, nitr
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A three dimensional model of a sub-
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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:
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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
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[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
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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
Page 522 and 523:
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
Page 534 and 535:
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
Page 540 and 541:
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.
Page 626 and 627:
1. Introduction The long-term radio
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Ce Ce 3+ Cl - Cl 2 The voltammogram
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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
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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
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Figure 1a. Zetapotential of NTA-mod
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Scheme 7. Magnetic silica particles
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[13] L.H. Delmau, N. Simon, M.J. Sc
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1. Introduction 137 90 Extraction p
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Figure 3. Schematic drawing of the
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(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
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RECENT PROGRESSES ON PARTITIONING S
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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
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1. Introduction Among the large num
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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
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6. The neutron escape line The comm
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Figure 7. Neutron background at the
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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
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
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HIGH AND INTERMEDIATE ENERGY NUCLEA
Page 773 and 774:
eactions, since the pre-equilibrium
Page 775 and 776:
calculate the very short-lived radi
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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
Page 791 and 792:
Figure 8. 10 B depletion in HYPER-H
Page 793:
POSTER SESSION TRANSMUTATION SYSTEM
Page 796 and 797:
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
Page 802 and 803:
e transmuted in BR2 hence remain va
Page 804 and 805:
Table 6. Atom percent concentration
Page 806 and 807:
advantage, with respect to FRs, of
Page 809 and 810:
ENHANCEMENT OF ACTINIDE INCINERATIO
Page 811 and 812:
Here Σ fC , ( E) are the fission a
Page 813 and 814:
pellet and the steel cladding. In o
Page 815 and 816:
Table 3.Neutronics parameters of hy
Page 817 and 818:
Figure 3. Neutron spectra averaged
Page 819 and 820:
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
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Following the normal procedure for
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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
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management. The major developments
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REFERENCES [1] H.J. MacPherson, Dev
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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
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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
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Table 1. Radiotoxicity of actinides
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INTERNATIONAL CO-OPERATION ON CREAT
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an international base to combine ef
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• Second topic: interaction of pr
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1. Introduction The role of acceler
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MEPI within the framework of Projec
Page 893 and 894:
NEW ORIGINAL IDEAS ON ACCELERATOR D
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During conceptual investigations of
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delay, interface and computer. The
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2. Channel-vessel design of ADS bla
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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
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Table 3. Radiotoxicity in americium
Page 910 and 911:
Table 5. Characteristics of station
Page 912 and 913:
1. Introduction The atomic power en
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of lead-bismuth target are given in
Page 917 and 918:
CRITICAL AND SUB-CRITICAL GT-MHRs F
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Table 1. Basic GT-MHR reactor param
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Figure 2. Typical change of the ave
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Scenario S4. This case is actually
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Figure 3. A change in radiotoxicity
Page 927:
[13] P. Goberis, Modelling of Innov
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1. Introduction The Nuclear Enginee
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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
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1. Introduction Actually, we notice
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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
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1. Background Radiation background
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the long-term hazard of spent fuel,
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In a transmutation fuel cycle inclu
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Figure 4. Potential biological haza
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cooling prior to SF reprocessing an
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REFERENCES [1] White Book of Nuclea
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ORDER FORM OECD Nuclear Energy Agen
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