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Table 5. Assumptions for transmutation strategies compared by <strong>OECD</strong>/NEA Strategies Reactor/ADS Fuel Av. burn-up (GWd/t HM ) Reprocessing method Recovery yield (%) All a, b b c d LWR (N4) FR (CAPRA) MA Burner, ADS TRU Burner, IFR TRU Burner, ADS UOX/MOX MOX AcN-ZrN Ac-Zr Ac-Zr 50 185 140 140 140 wet wet dry dry dry 99.9 99.9 99.9 99.9 99.9 6. Fission product transmutation The neutron capture process is currently the only promising nuclear reaction for transmuting fission products. Other processes which have been proposed in the past rely on technologies which are still at a very early stage of development (e.g. fusion neutron sources) and generally suffer from a poor energy balance. The capture process consumes neutrons but, theoretically, fast reactors could deliver enough surplus neutrons to allow the potentially troublesome long-lived fission products to be completely transmuted to shorter-lived or stable species (cf. Table 1). The transmutation of a fission product makes sense only if the reaction rate (microscopic crosssection times neutron flux) is higher than the natural decay rate of the nuclide. With the practically achievable neutron fluxes, this condition cannot be met for the most abundant fission products 137 Cs and 90 Sr with half-lives of only about 30 years, i.e. these fission products are “non-transmutable”. However, since their radioactive life is limited to less than 300 years, they can be safely enclosed using engineered barriers only. On the other hand, the fission products determine the size of the vitrified waste repository which, consequently, cannot be much reduced by P&T operations. The fission products which influence the long-term risk of a repository are, in order of radiologic importance, 129 I, 99 Tc, 135 Cs, 93 Zr, and 126 Sn. Activation products ( 14 C and 36 Cl) can also contribute to the dose. Obviously, the relative contribution of these nuclides to the integral risk varies according to the type of repository host rock. In the following, the problems associated with the transmutation of these five fission products are discussed separately. It should be noted that the determination of the separation yield and the decontamination factor (DF) for HLW depends to a great extent on policy decisions and that, depending on the nuclide, special conditioning and confinement is an alternative to transmutation. 6.1 Iodine-129 (T 1/2 = 1.6·10 7 a) In most of the direct storage concepts for spent fuel, 129 I is the first nuclide to enter into the biosphere due to its very high mobility. During aqueous reprocessing, iodine is removed from the dissolver solution with a yield of 95-98%. To improve the separation yield, more complex chemical treatments are necessary. Better separation yields may also be achieved with high-temperature pyrochemical processes. Special methods for conditioning in the form of AgI, PbIO4, etc. have been developed but, because of the extremely long half-life, the eventual migration to the environment cannot be excluded. 44
Since the radiotoxicity of 129 I is the highest of the fission products and equivalent to that of actinides, it would be advisable to increase the separation yield to achieve a DF of about 1 000. The necessity of an isotopic separation and the limited stability of the target material, however, make the transmutation of 129 I difficult, and conditioning and confinement seems to be the best method to reduce its radiological impact. Nevertheless, the present method of diluting iodine in the sea may still be defendable because of the enormous dilution of 129 I in the (natural) 127 I present in seawater. The storage in a salt dome, consisting of evaporated seawater, is an another alternative which still has its merits. 6.2 Technetium-99 (T1/2 = 2.1·10 5 a) The radiologic significance of 99 Tc is important if the repository surroundings are slightly oxidic. In reducing conditions 99 Tc is remarkably stable and insoluble as technetium metal or TcO2 suboxide. Partitioning of 99 Tc is not an easy task because it occurs as insoluble metal and as soluble technetate ion in solution. Separation from aqueous effluents is possible in an advanced PUREX scheme, but recovery from insoluble residues is difficult, with the present recovery yield at best reaching 80%. Improving this yield significantly implies the development of new separation technologies such as the not yet proven conversion of the technetium into a single chemical species. Alternatively, a group separation together with the platinum metals may be carried out using pyrometallurgical processes. If separated in metallic form, transmutation appears to be feasible because of its stability and relatively large neutron capture cross-section. 6.3 Caesium-135 (T1/2 = 2.3·10 6 a), Zirconium-93 (T1/2 = 1.5·10 6 a) and Tin-126 (T1/2 = 1.0·10 5 a) Caesium occurs in the form of the isotopes 133 (stable), 135 and 137. In terms of radiologic significance, 137 Cs is the major constituent of HLW (see above). The activity of the long-lived 135 Cs in HLW is a million times lower. However, once released from a matrix as glass, caesium is very mobile. Transformation of 135 Cs to stable 136 Ba is possible from a neutronics point of view, but probably impracticable because a close to 100% isotopic separation efficiency would be required (traces of 133 Cs in the target would generate new 135 Cs during the irradiation). Zirconium-93 is somewhat similar to 135 Cs, it has also a very long half-life and a small isotopic abundance (about 14% of the total Zr). An isotopic separation would be necessary, and its transformation to stable 94 Zr would be very slow because the thermal capture cross-section is about five times smaller than that of 135 Cs. Tin-126 is partly soluble in HLW from aqueous reprocessing but occurs also as an insoluble residue, similar to technetium. Isolation involves a special treatment of the HLW, and the use of isotopic separation techniques. Transmutation of 126 Sn is questionable due to the very low neutron capture cross-section. 7. Consequences for geologic disposal As mentioned before, the primary concern of geologic repositories are possible releases of the relatively mobile fission products. Since the fission product yields are not very sensitive to the fuel composition and the neutron spectrum of the reactor, the fission product risk depends primarily on the number of fissions, i.e. the energy, produced in the fuel. This means that the fission product risk cannot be much influenced by the actinide transmutation strategy and can only be mitigated by 45
Page 1 and 2: Nuclear Development ACTINIDE AND FI
Page 3 and 4: FOREWORD The objective of the OECD/
Page 5 and 6: TABLE OF CONTENTS Foreword ........
Page 7 and 8: EXECUTIVE SUMMARY More than 160 par
Page 9: identified. In the fuel area, labor
Page 12 and 13: 17:20-19:05 Session III: Partitioni
Page 14 and 15: Poster sessions Poster session: Par
Page 17 and 18: WELCOME ADDRESS Lucila Izquierdo Ge
Page 19 and 20: WELCOME ADDRESS Michel Hugon Co-ord
Page 21 and 22: WELCOME ADDRESS Philippe Savelli De
Page 23: developments. This will surely beco
Page 26 and 27: use of FBRs for transmutation toget
Page 28 and 29: view, i.e. better use of uranium an
Page 30 and 31: W. Forsberg proposes to reduce the
Page 32 and 33: 1. From the open fuel cycle to the
Page 34 and 35: Figures 2 and 3 show the radiotoxic
Page 36 and 37: Denoting the transuranic (TRU) or m
Page 38 and 39: or, in terms of the fuel burn-up an
Page 40 and 41: quantities of LWR-MOX and FR-MOX wi
Page 42 and 43: view of the historic development, t
Page 46 and 47: separating troublesome fission prod
Page 48 and 49: REFERENCES [1] L.H. Baetslé, Ch. D
Page 51 and 52: SESSION III Partitioning Chairs: J.
Page 53 and 54: OVERVIEW OF THE HYDROMETALLURGICAL
Page 55 and 56: 2.1.3 Consequences Owing to the fac
Page 57 and 58: The extraction and separation mecha
Page 59 and 60: extractant was observed. As a conse
Page 61 and 62: 2.3.2 Examples of strategies and
Page 63 and 64: 3. Conclusions and perspectives 3.1
Page 65 and 66: SESSION IV Basic Physics, Materials
Page 67 and 68: TRANSMUTATION: A DECADE OF REVIVAL
Page 69 and 70: 2.1 The IFR concept and the homogen
Page 71 and 72: 2.3 Dedicated systems Making again
Page 73 and 74: compound “macro-dispersed” in M
Page 75 and 76: Figure 3. Sketch of ADS, liquid met
Page 77 and 78: 3.3.2.1 The MEGAPIE project [40] ME
Page 79 and 80: 3.3.2.2 The MUSE experiments The MU
Page 81 and 82: Figure 8. Comparison of the neutron
Page 83 and 84: Figure 9. Scenarios at equilibrium
Page 85 and 86: goals in this field. Since once-thr
Page 87 and 88: • The use of Thorium in PWRs alwa
Page 89 and 90: • Understanding of the role of AD
Page 91 and 92: [17] Y. Arai, T. Ogawa, Research on
Page 93: SESSION V Transmutation Systems and
Page 96 and 97:
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
Page 123:
To conclude, this poster session in
Page 126 and 127:
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.
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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
Page 451 and 452:
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
Page 464 and 465:
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
Page 492 and 493:
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
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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
Page 532 and 533:
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
Page 552 and 553:
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
Page 595 and 596:
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
Page 618 and 619:
Plutonium was simulated with the no
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The influence of uranium and pluton
Page 622 and 623:
The influence of uranium and pluton
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REFERENCES [1] I.I. Nazarenko, A.M.
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1. Introduction The long-term radio
Page 628 and 629:
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
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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
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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
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1. Introduction A heavy-water CANDU
Page 670 and 671:
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
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trace amount of Am and Eu. The HBTM
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6. Conclusion Declassification of t
Page 681:
POSTER SESSION BASIC PHYSICS: NUCLE
Page 684 and 685:
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
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
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[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
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1. Introduction During the past few
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(same surface and 0.5 mm thickness)
Page 746 and 747:
Figure 2. Dependence of the total a
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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
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Figure 1. Excited states of 209 Bi
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Figure 3. The fission probability o
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MEASUREMENT OF DOUBLE DIFFERENTIAL
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Figure 1. Global view of the experi
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To get the proton (deuteron) energy
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3.1 Corrections Several corrections
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Figure 11. Active target fraction (
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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
Page 791 and 792:
Figure 8. 10 B depletion in HYPER-H
Page 793:
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
Page 800 and 801:
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
Page 821:
REFERENCES [1] ANSALDO Technical Re
Page 824 and 825:
1. Introduction At present, there a
Page 826 and 827:
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
Page 832 and 833:
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
Page 841 and 842:
MOLTEN SALTS AS POSSIBLE FUEL FLUID
Page 843 and 844:
2. The fuel salt for MSB concept Ma
Page 845 and 846:
and minor actinides must be removed
Page 847 and 848:
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
Page 856 and 857:
Table 1. Main parameters of the EAD
Page 858 and 859:
Table 5. Neutron balance in the who
Page 860 and 861:
Table 7. Neutron flux distributions
Page 862 and 863:
Table 8. Displacement rates DPA/yea
Page 865 and 866:
DEEP UNDERGROUND TRANSMUTOR (PASSIV
Page 867 and 868:
passive state. By operating at a hi
Page 869 and 870:
I have proposed using an accelerato
Page 871 and 872:
Figure 1. Layout of deep undergroun
Page 873 and 874:
RADIATION CHARACTERISTICS OF PWR MO
Page 875 and 876:
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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