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Am+Cm/Ln(III) separation, (iv) the SESAME process for Am/Cm separation, (v) the CALIX- CROWN process for Cs separation. In some organisations (e.g. in USA, Japan, Czech Republic or Russian Federation), instead of developing a succession of separation processes for peculiar LLRNs, the integration of processes for MAs and FPs extraction are studied. For example, the use of a solvent containing a mixture of cobalt dicarbollide+dioxide of diphosphine allows the combined extraction of Cs+Sr+(Am+Cm)+Ln. 2.2.2 Minor actinides partitioning One cycle processes • DIDPA process (JAERI, Japan) This process for MAs partitioning is based on the use of di-isodecylphosphoric acid (DIDPA). The extraction mechanism is the following: n+ M + n (HA) ⇔ M(HA ) + n H (1) 2 2 n + The separation of the TRU elements is done by successive stripping from the loaded solvent, including the use of diethylenetriaminopentaacetic acid (DTPA) complexing agent for actinides(III)/Ln(III) separation (TALSPEAK like process, vide infra). The DIDPA process was recently tested successfully in the BECKY hot-cell at NUCEF (JAERI, Tokai-Mura). Among the possible drawbacks of this process one can mention the: (i) required feed acid adjustment, (ii) solvent degradation and its delicate clean-up, (iii) limited solvent loading with metal ions. • SETFICS (JNC, Japan) The SETFICS process constitutes a modification of the TRUEX process (vide infra) based on the use of the extractant di-isobutyl-phenyl-octylcarbamoylmethylphosphine oxide (ΦC8H17P(O)CH2C(O)(i-C4H9)2 = CMPO) The extraction mechanism is as follows: n+ - M + n NO + m CMPO ⇔ M(NO ) (CMPO) (2) 3 3 n m The separation of TRUs is done by successive stripping from the loaded solvent, including also the use of DTPA for An(III)/Ln(III) separation. This process has not been tested yet with genuine HAWs. The possible drawbacks of this process are: (i) the limited stripping efficiency, (ii) the management of salts and DTPA containing effluents. • PALADIN (CEA, France) This process is based on the use of a mixture of extractants: a malonamide (DIAMEX process extractant)+di-ethylhexylphosphoric acid (HDEHP), the extractant of the TALSPEAK process. 56
The extraction and separation mechanisms are the following: Extraction: 3+ − M + 3NO + 2 DIAM ⇔M(NO ) (DIAM) (3) 3 3 3 2 An(III)/Ln(III) separation: done after contacting the loaded solvent with a pH adjusted aqueous solution containing DTPA selective trivalent actinide complexing agent. For pH range HDEHP is the extractant, while at the metal nitrate extraction step, carried out with acidic feeds 3 to 5 mol/L in nitric acid, trivalent An and Ln are extracted with the malonamide. This process was recently successfully tested in the ATALANTE facility (CEA/Marcoule, France). The possible drawbacks of this process are the: (i) necessity to use 2 extractants, (ii) need of pH adjustment, (iii) co-extraction of numerous ions, (iv) solvent clean-up not yet defined. Multi-cycle processes • 1 st step: An+Ln co-extraction TRUEX (USA, Japan, Russian Federation, Italy and India) This process is based on the use of the CMPO extractant. This process was developed by Horwitz (ANL) and Schulz (Hanford) in the USA in the 80s. The advantages of the TRUEX process are the following: (i) it can extract An (and Ln) salts from acidic feeds, (ii) its efficiency has been demonstrated with genuine HAWs, (iii) a large experience has been gained worldwide. The main drawbacks of the TRUEX process are the: (i) necessity to use large concentration of tri-n-butylphosphate (TBP) as solvent modifier added to the solvent to prevent third phase formation, (ii) stripping of metal ions which are not so efficient, (iii) delicate solvent clean-up. DIAMEX (France, Italy, Germany, Europe, Japan, USA and India) This process is based on the use of a malonamide extractant. The main interests of the process are: (i) An (and Ln) salts can be extracted from acidic feeds, (ii) its efficiency has been demonstrated on genuine HAWs, (France, Europe), (iii) no secondary solid wastes generated owing to the CHON character of the malonamide extractant. Its main drawback relies in the partial co-extraction of palladium (Pd) and ruthenium (Ru) with the MAs. A process based on a new type of diamide, a diglycolamide (DGA), which is a terdendate ligand having better affinity for An(III) than the malonamide, is under development at JAERI (Tokai, Japan). TRPO (INET, Tsinghua University, China) The TRPO process is based on the use of a mixture of tri-alkyl phosphine oxides (R3P(O), with R = alkyl groups) as extractant. This process has been tested successfully in China with genuine HAW. Its main drawbacks concern the necessity: (i) to adjust the feed acidity, (ii) to use a concentrated nitric acid solution for An(III)+Ln(III) stripping, which complicates the subsequent An(III)/Ln(III) partitioning step. 57
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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 44 and 45: Table 5. Assumptions for transmutat
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: 2.1.3 Consequences Owing to the fac
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
Page 98 and 99: • Safety should be “designed in
Page 100 and 101: 3. Minor actinide and/or transurani
Page 102 and 103: Table 2. Values of Dj (neutron cons
Page 104 and 105: Table 4. Delayed neutron fraction I
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Figure 4. η (Neutrons released per
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Table 5. ADS Distinguishing feature
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While a favourable ADS safety featu
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Optimised mixes of MA and Pu can be
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Moreover, the fuel is where neutron
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REFERENCES [1] L. Van den Durpel et
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[19] D.C. Wade and E. Fujita, Trend
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POSTER SESSION Basic Physics: Nucle
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To conclude, this poster session in
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Five other papers related to ADS co
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SESSION I OVERVIEW OF NATIONAL AND
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1. Current activities for radioacti
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3.2 Results to date and analyses of
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3.2.5.2 JNC JNC is considering the
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4.6 Short-term increase in radiatio
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Annex 1 R&D scheme for partitioning
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Annex 3 Members of the Advisory Com
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plutonium can be recycled in pressu
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choices and the implementation of m
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1. Introduction Since the 5th Infor
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strata” approach which would invo
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IAEA ACTIVITIES IN THE AREA OF EMER
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actually started to do so) because
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establishment of an international R
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The accelerator driven transmutatio
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substantiate this recommendation, s
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current, advanced and innovative nu
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ACCELERATOR DRIVEN SUB-CRITICAL SYS
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demonstration of feasibility of a E
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An extended “skeleton” for ADS
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• Fertile support (uranium) is no
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7. Conclusions The TWG under the ch
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1. Introduction The priorities for
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In the EURATOM Fourth Framework Pro
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Table 2. Cluster on transmutation-t
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6. Community research for the perio
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REFERENCES [1] “Council Decision
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1. Introduction Back in 1989, the O
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would need the continuation of tech
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individual isotopes as a function o
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Therefore, while there is continuin
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[9] OECD/NEA, Overview of Physics A
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RECENT TOPICS IN R&D FOR THE OMEGA
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Figure 1. Partitioning and transmut
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The present 4-GPP necessitates a pr
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5. Concluding remarks In 1999, the
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REFERENCES [1] T. Mukaiyama, T. Tak
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1. Introduction CIEMAT is actively
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adiotoxicity to be managed could al
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Figure 3. Mass composition of the d
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Figure 6. Fuel cycle assumed in the
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the 4 batches scheme, allowing to a
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Figure 11. Transmutation efficiency
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1. Introduction Spent fuels of mode
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Figure 3. A change in radiotoxicity
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These dependencies are shown on Fig
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When increasing the moderator fract
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Even greater power increases are ob
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The effect of a moderator volume fr
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Table 11. Different isotopes contri
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Thus the transmutation of such FPs
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ASSESSMENT OF NUCLEAR POWER SCENARI
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elease probabilities. The time dist
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Table 2. Annual heavy nuclide contr
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Figure 3. Reduction of potential ra
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DISPOSAL OF PARTITIONING-TRANSMUTAT
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Figure 2. Decay heat from SNF 2000
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Figure 3. Shorter-lived HHR reposit
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4. Management of low-heat, long-liv
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isotope from other caesium isotopes
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THE AMSTER CONCEPT J. Vergnes 1 , D
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Figure 1. Layout diagram of the mol
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Table 1. Definition of configuratio
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We therefore adopted a partial purg
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conceivable. Thus by increasing the
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6. R&D needed to validate the AMSTE
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SESSION III PARTITIONING J.P. Glatz
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PARTITIONING-SEPARATION OF METAL IO
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The terpyridyl reagent (ligand L 1
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Figure 2. The synthesis of ADTPTZ a
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2.4 Implications for partitioning T
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SEPARATION OF MINOR ACTINIDES FROM
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installed in a hot cell. The feed w
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the concentrations of U, Pu and Np
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Table 2 shows the recovery in the r
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PARTITIONING ANIONIC AGENTS BASED O
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which of these, the Co 3+ , Fe 3+ a
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This dianionic species must be extr
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Figure 6 Ph 2 P acetone PPh 2 H2 O
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Figure 9 H 3 C RO(CH 2 )n CH 3 (CH
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[7] J. Rais and P. Selucky, Nucleon
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PYROCHEMICAL PROCESSING OF IRRADIAT
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The metallic cadmium product of the
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Figure 2. Schematic flow-sheet for
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R&D OF PYROCHEMICAL PARTITIONING IN
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(first of all pumps) for fluoride m
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4. Research on material and equipme
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REFERENCES [1] Uhlir J., Pyrochemic
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1. Introduction The increasing inte
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Figure 2. Stainless steel box with
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Figure 4. U deposit on solid cathod
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Figure 7. Schematic flow of the cou
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actinide elements from spent (metal
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DEVELOPMENT OF PLUTONIUM RECOVERY P
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uranium dendrite and that uranium c
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Table 1. Conditions and results of
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Cathode potential went down to -1.6
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Figure 6. Change of LCC potential i
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Figure 9. Relation between Pu conce
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consideration described in the prec
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[13] Y. Arai, S. Fukushima, K. Shio
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SESSION IV BASIC PHYSICS, MATERIALS
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1. Introduction The reduction of th
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agrees ours within limits of errors
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Figure 1. Thermal neutron capture c
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[18] A.P. Baerg, R.M. Bartholomew,
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1. Introduction Nowadays it is well
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In order to describe the inter-nucl
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kind of measurements allow to chara
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Figure 6. Two-dimensional cluster p
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Figure 8. Excitation functions for
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REFERENCES [1] D. Ridikas, thesis,
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1. Introduction Since 1991, the Com
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Experimental reactivity control tec
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Table 2. Neutron intensities Target
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experimental channels (horizontal a
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376
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Table 3. Planned experimental progr
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1. Introduction and benchmark speci
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neutrons. Since the neutron flux is
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Figure 2. Microscopic capture cross
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Figure 4. k eff variation in the st
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2.4 Neutron flux distribution One r
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etween the highest and the lowest v
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The isotope specific β eff values
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SESSION IV BASIC PHYSICS, MATERIALS
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1. Introduction Due to its excellen
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Figure 2. Tests scheme 0 340 h. 1 0
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Figure 4. Auger depth profile conce
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Figure 8. Auger depth profile conce
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deposited at the cold zone, and the
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inner layer grows inward from the o
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[8] V.M. Fedirko, O.I. Eliseeva, V.
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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
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1. Introduction Research and develo
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Table 2. Core design parameters for
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2.2 Representation of MA transmutat
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Figure 1(b) shows the cases for the
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It is found that the higher MA tran
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REFERENCES [1] T. Ikegami, H. Hayas
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1. Introduction The management of t
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Table 1. Core performance of MA and
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Figure 3. Nuclear electricity capac
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Table 3. Experimental items at PEF
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REFERENCES [1] Takano H., Akie H.,
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1. Introduction and background The
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neutron source, the reactor can mai
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atoms. For fuel region Rf = 2.5 cm,
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Figure 3. Neutron flux spectra for
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A possible way to maintain the k ef
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higher than 99% of 239 Pu, and high
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TRANSMUTATION OF NUCLEAR WASTES WIT
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Figure 1. PBT conceptual view Table
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very tight holders for fission frag
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5. Cooling system A preliminary des
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spectral densities [10,11] and can
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MYRRHA, A MULTI-PURPOSE ADS FOR R&D
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hexagonal assemblies of 122 mm plat
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to achieve the requested performanc
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3 MYRRHA associated R&D programme F
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collaboration with Forschungszentru
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• Industrial partners, in particu
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1. Introduction The transmutation o
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Existing accelerators have been des
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suggested to look for an innovative
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Table 1. Main lead-bismuth eutectic
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4.3 The core The basic fuel sub-ass
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Figure 1. Experimental accelerator
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HELIUM-COOLED REACTOR TECHNOLOGIES
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of its potential use in nuclear wea
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Figure 2. Neutron flux distribution
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atio. Given this rate of destructio
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Figure 5. Irradiated TRISO particle
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in ceramic-coated microspheres of t
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(LOCA) event. The effect on this fe
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Figure 13. Elevation AD-FMHR The fa
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Deep burn-up of 239 Pu and fissiona
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POSTER SESSION PARTITIONING M.J. Hu
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1. Introduction The study of the be
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Plutonium was simulated with the no
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The influence of uranium and pluton
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The influence of uranium and pluton
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REFERENCES [1] I.I. Nazarenko, A.M.
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1. Introduction The long-term radio
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Ce Ce 3+ Cl - Cl 2 The voltammogram
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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
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[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
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1. Introduction Over the recent yea
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2.3.2 Set-up We set up a single HFM
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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
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REFERENCES [1] Kyrš M., +H PiQHN S
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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
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trace amount of Am and Eu. The HBTM
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6. Conclusion Declassification of t
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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
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Table 1. Parameters of the two coll
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Figure 4. Radial distribution of th
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6. The neutron escape line The comm
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Figure 7. Neutron background at the
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RECENT CAPTURE CROSS-SECTIONS VALID
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Figure 1. The GENEPI accelerator an
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2.3.3 Neutron flux measurements •
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Figure 6. Time spectrum of 3 He gas
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4. Analysis 4.1 Background subtract
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Figure 11. ENDF/B-VI, JEF2.2 and JE
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DOUBLE DIFFERENTIAL CROSS-SECTION F
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3. Conclusion Double differential c
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Figure 3. Preliminary results of do
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MEASUREMENTS OF PARTICULE EMISSION
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2. Experimental set-up The experime
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4. Results Figure 3 presents neutro
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1. Introduction Intermediate-energy
Page 724 and 725:
Table 1. Relative neutron-induced c
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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,
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NUCLEON-INDUCED FISSION CROSS-SECTI
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Figure 1. Scheme of the new code Z
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Figure 3. Neutron-induced fission c
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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)
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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
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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
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HIGH AND INTERMEDIATE ENERGY NUCLEA
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eactions, since the pre-equilibrium
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calculate the very short-lived radi
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cross-sections; the secondary react
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All possible nuclear reactions will
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A STUDY ON BURNABLE ABSORBER FOR A
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2. Burnable absorber for HYPER 2.1
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Table 2. One-group effective cross-
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of the core, is directly determined
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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
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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
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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
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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
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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
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[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
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Table 5. Characteristics of station
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1. Introduction The atomic power en
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of lead-bismuth target are given in
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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
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[13] P. Goberis, Modelling of Innov
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1. Introduction The Nuclear Enginee
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Some simplifications have been made
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Figure 3. Velocity vectors Some of
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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
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The evaluations obtained in [2] hav
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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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