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1. Introduction A heavy-water CANDU-type reactor has good neutron-physical characteristics due to the use of heavy water as moderator and coolant. In particular, it allows using natural uranium as nuclear fuel, whereas in other types of thermal neutron reactors, it is necessary to use uranium with enrichment of several percents. In natural uranium fuel, the relative role of plutonium produced from 238 U is great. Nevertheless, fuel burn-up and lifetime are small because fuel multiplying properties at burning out are quickly reduced. One of the opportunities to increase the lifetime is the transition to nuclear fuel with slight enrichment. Another opportunity, intermediate chemical processing of fuel can be considered where the fission products are removed and fuel nuclides are recycled for further burning. For the future atomic power, a nuclear fuel cycle on base of 232 Th- 233 U can be rather perspective. Thorium cycle has essential advantages over traditional uranium – plutonium cycle because of considerably less amount of transuranium long-lived radioactive wastes (though considerably more amount of rather harmful 232 U). In CANDU reactors, operation in thorium cycle and, the intermediate fuel cleaning of the fission products could also prolong lifetime and lower the requirement of specially obtained 233 U. In this paper, results are given of a calculation study of the influence of intermediate chemical processing of nuclear fuel with removal of fission products on fuel lifetime and burn-up in CANDUtype reactor are given. Uranium fuel on basis of natural and slightly enriched uranium (with enrichment up to 1.4%) and thorium fuel on base of 232 Th- 233 U are considered. 2. Calculation model The reactor design is described in [1]. In an active core, 380 fuel assemblies are placed. Every assembly contains 37 uranium pins with zirconium cladding in zirconium tube. Heavy water is used as the coolant and moderator. Fuel assemblies are located in a square lattice with a pitch of 23.5 cm. Height of an active core is 594 cm. Natural uranium loading in reactor is 114 tonnes. It was accepted in calculations that reactor multiplying properties can be approximately described by multiplication factor of an elementary cell as follows. Multiplication factor of an elementary cell k eff varies in function of fuel burn-up. The reactor operates in a mode of continuous refuelling. Fuel assemblies with various burn-up from fresh fuel up to maximum burn-up are situated in core at every moment. The on-load refuelling is carried out independently in different channels after achieving the maximal burn-up. It allows accepting the value of multiplication factor in an elementary cell average over fuel lifetime with correction on neutrons leakage from reactor as approximate reactor multiplication factor. Such approximation is quite justified for comparative calculations of the effect of intermediate nuclear fuel cleaning. At calculations of lifetime, it was considered that the neutrons leakage makes 1% and the value = 1.01 was accepted. In reactors with continuous refuelling at constant power, the value of neutron flux varies in time very slightly. It is necessary that the power of one fuel assembly varies in time because of changing of fissile nuclide amount, and the fuel assemblies with different burn-up have appreciably different power. Calculations of fuel burn-up and transformation of isotopes were carried out at constant neutron flux. 668
3. Natural or slightly enriched uranium fuel The calculations of reaction rates and multiplication factor in an elementary cell were performed with the code [2]. A fuel assembly with pins was represented as a 4-ring coaxial assembly with the same volumes of all-structural materials and fuel loading. The enrichment of uranium from 0.714% up to 1.4% was considered. The amount of uranium in fresh fuel assembly was accepted the same for all enrichments, and the 235 U amount corresponded to the enrichment. For natural uranium fuel, thermal neutrons flux was equal to Φ = 5 10 13 n/cm 2 s. Neutron flux for the enriched fuel was determined in a way to get the same power of fresh fuel assembly as in the variant with natural uranium. At calculations of nuclide transformation, isotopes of uranium, neptunium, plutonium, americium and curium up to 244 Cm were taken into account. In uranium fuel, 239 Pu is produced. This isotope gives the essential contribution in reactivity of CANDU-type reactor with natural or slightly enriched fuel already in the initial period of fuel lifetime. The dependence of multiplication factor k eff in an elementary cell on irradiation time T was calculated for initial enrichment of uranium from 0.714% up to 1.4% without intermediate cleaning. The neutron capture by fission products was taken into account by means of an “effective fission fragment” [3]. A poisoning by 135 Xe, 105 Rh and absorption of neutrons by 149 Sm and 151 Sm were additionally taken into account. The fuel lifetime T f was determined by value = 1.01. Table 1, fuel lifetime T f and burn-up FP defined by amount of fission products in 1 tonne of fuel without intermediate cleaning for different initial uranium enrichment C. Table 1. Fuel lifetime T f and burn-up FP without intermediate cleaning C, % 0.714 1.0 1.2 1.4 T f , years 2.0 2.8 5.38 6.67 FP, kg/tonne 11.4 17.4 20.8 23.4 Analogous time dependence of multiplication factor in an elementary cell k eff with intermediate processing with cleaning from accumulated fission products was calculated for natural uranium fuel and fuel with enrichment 1%. The intermediate processing was carried out at time T p = 0.8, 1.2, 1.6 years. For enrichment 1%, the intermediate processing was carried out also at T p = 2 and 2.4 years. These data allow to estimate fuel lifetime corresponding to average over lifetime multiplication factor = 1.01. They are presented in Table 2. T p = 0 corresponds to the mode without intermediate cleaning. Table 2. Fuel lifetime T f and burn-up FP with intermediate processing T p , years C = 0.714% C = 1.0% T f , years FP, kg/ton T f , years FP, kg/ton 0.0 2.0 11.4 3.9 17.4 0.8 2.52 13.8 4.71 19.9 1.2 2.4 13.3 4.76 20.1 1.6 2.4 13.3 4.69 19.8 2.0 – – 4.57 19.5 2.4 – – 4.41 19.0 669
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Nuclear Development ACTINIDE AND FI
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FOREWORD The objective of the OECD/
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TABLE OF CONTENTS Foreword ........
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EXECUTIVE SUMMARY More than 160 par
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identified. In the fuel area, labor
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17:20-19:05 Session III: Partitioni
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Poster sessions Poster session: Par
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WELCOME ADDRESS Lucila Izquierdo Ge
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WELCOME ADDRESS Michel Hugon Co-ord
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WELCOME ADDRESS Philippe Savelli De
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developments. This will surely beco
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use of FBRs for transmutation toget
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view, i.e. better use of uranium an
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W. Forsberg proposes to reduce the
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1. From the open fuel cycle to the
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Figures 2 and 3 show the radiotoxic
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Denoting the transuranic (TRU) or m
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or, in terms of the fuel burn-up an
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quantities of LWR-MOX and FR-MOX wi
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view of the historic development, t
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Table 5. Assumptions for transmutat
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separating troublesome fission prod
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REFERENCES [1] L.H. Baetslé, Ch. D
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SESSION III Partitioning Chairs: J.
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OVERVIEW OF THE HYDROMETALLURGICAL
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2.1.3 Consequences Owing to the fac
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The extraction and separation mecha
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extractant was observed. As a conse
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2.3.2 Examples of strategies and
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3. Conclusions and perspectives 3.1
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SESSION IV Basic Physics, Materials
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TRANSMUTATION: A DECADE OF REVIVAL
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2.1 The IFR concept and the homogen
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2.3 Dedicated systems Making again
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compound “macro-dispersed” in M
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Figure 3. Sketch of ADS, liquid met
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3.3.2.1 The MEGAPIE project [40] ME
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3.3.2.2 The MUSE experiments The MU
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Figure 8. Comparison of the neutron
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Figure 9. Scenarios at equilibrium
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goals in this field. Since once-thr
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• The use of Thorium in PWRs alwa
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• Understanding of the role of AD
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[17] Y. Arai, T. Ogawa, Research on
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SESSION V Transmutation Systems and
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1. Introduction The term ADS compre
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• Safety should be “designed in
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3. Minor actinide and/or transurani
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Table 2. Values of Dj (neutron cons
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Table 4. Delayed neutron fraction I
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Figure 4. η (Neutrons released per
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Table 5. ADS Distinguishing feature
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While a favourable ADS safety featu
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Optimised mixes of MA and Pu can be
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Moreover, the fuel is where neutron
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REFERENCES [1] L. Van den Durpel et
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[19] D.C. Wade and E. Fujita, Trend
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POSTER SESSION Basic Physics: Nucle
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To conclude, this poster session in
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Five other papers related to ADS co
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SESSION I OVERVIEW OF NATIONAL AND
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1. Current activities for radioacti
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3.2 Results to date and analyses of
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3.2.5.2 JNC JNC is considering the
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4.6 Short-term increase in radiatio
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Annex 1 R&D scheme for partitioning
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Annex 3 Members of the Advisory Com
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plutonium can be recycled in pressu
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choices and the implementation of m
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1. Introduction Since the 5th Infor
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strata” approach which would invo
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IAEA ACTIVITIES IN THE AREA OF EMER
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actually started to do so) because
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establishment of an international R
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The accelerator driven transmutatio
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substantiate this recommendation, s
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current, advanced and innovative nu
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ACCELERATOR DRIVEN SUB-CRITICAL SYS
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demonstration of feasibility of a E
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An extended “skeleton” for ADS
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• Fertile support (uranium) is no
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7. Conclusions The TWG under the ch
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1. Introduction The priorities for
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In the EURATOM Fourth Framework Pro
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Table 2. Cluster on transmutation-t
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6. Community research for the perio
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REFERENCES [1] “Council Decision
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1. Introduction Back in 1989, the O
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would need the continuation of tech
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individual isotopes as a function o
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Therefore, while there is continuin
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[9] OECD/NEA, Overview of Physics A
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RECENT TOPICS IN R&D FOR THE OMEGA
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Figure 1. Partitioning and transmut
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The present 4-GPP necessitates a pr
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5. Concluding remarks In 1999, the
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REFERENCES [1] T. Mukaiyama, T. Tak
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1. Introduction CIEMAT is actively
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adiotoxicity to be managed could al
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Figure 3. Mass composition of the d
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Figure 6. Fuel cycle assumed in the
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the 4 batches scheme, allowing to a
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Figure 11. Transmutation efficiency
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1. Introduction Spent fuels of mode
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Figure 3. A change in radiotoxicity
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These dependencies are shown on Fig
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When increasing the moderator fract
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Even greater power increases are ob
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The effect of a moderator volume fr
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Table 11. Different isotopes contri
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Thus the transmutation of such FPs
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ASSESSMENT OF NUCLEAR POWER SCENARI
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elease probabilities. The time dist
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Table 2. Annual heavy nuclide contr
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Figure 3. Reduction of potential ra
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DISPOSAL OF PARTITIONING-TRANSMUTAT
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Figure 2. Decay heat from SNF 2000
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Figure 3. Shorter-lived HHR reposit
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4. Management of low-heat, long-liv
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isotope from other caesium isotopes
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THE AMSTER CONCEPT J. Vergnes 1 , D
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Figure 1. Layout diagram of the mol
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Table 1. Definition of configuratio
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We therefore adopted a partial purg
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conceivable. Thus by increasing the
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6. R&D needed to validate the AMSTE
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SESSION III PARTITIONING J.P. Glatz
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PARTITIONING-SEPARATION OF METAL IO
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The terpyridyl reagent (ligand L 1
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Figure 2. The synthesis of ADTPTZ a
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2.4 Implications for partitioning T
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SEPARATION OF MINOR ACTINIDES FROM
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installed in a hot cell. The feed w
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the concentrations of U, Pu and Np
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Table 2 shows the recovery in the r
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PARTITIONING ANIONIC AGENTS BASED O
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which of these, the Co 3+ , Fe 3+ a
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This dianionic species must be extr
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Figure 6 Ph 2 P acetone PPh 2 H2 O
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Figure 9 H 3 C RO(CH 2 )n CH 3 (CH
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[7] J. Rais and P. Selucky, Nucleon
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PYROCHEMICAL PROCESSING OF IRRADIAT
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The metallic cadmium product of the
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Figure 2. Schematic flow-sheet for
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R&D OF PYROCHEMICAL PARTITIONING IN
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(first of all pumps) for fluoride m
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4. Research on material and equipme
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REFERENCES [1] Uhlir J., Pyrochemic
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1. Introduction The increasing inte
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Figure 2. Stainless steel box with
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Figure 4. U deposit on solid cathod
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Figure 7. Schematic flow of the cou
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actinide elements from spent (metal
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DEVELOPMENT OF PLUTONIUM RECOVERY P
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uranium dendrite and that uranium c
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Table 1. Conditions and results of
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Cathode potential went down to -1.6
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Figure 6. Change of LCC potential i
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Figure 9. Relation between Pu conce
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consideration described in the prec
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[13] Y. Arai, S. Fukushima, K. Shio
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SESSION IV BASIC PHYSICS, MATERIALS
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1. Introduction The reduction of th
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agrees ours within limits of errors
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Figure 1. Thermal neutron capture c
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[18] A.P. Baerg, R.M. Bartholomew,
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1. Introduction Nowadays it is well
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In order to describe the inter-nucl
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kind of measurements allow to chara
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Figure 6. Two-dimensional cluster p
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Figure 8. Excitation functions for
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REFERENCES [1] D. Ridikas, thesis,
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1. Introduction Since 1991, the Com
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Experimental reactivity control tec
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Table 2. Neutron intensities Target
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experimental channels (horizontal a
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376
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Table 3. Planned experimental progr
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1. Introduction and benchmark speci
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neutrons. Since the neutron flux is
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Figure 2. Microscopic capture cross
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Figure 4. k eff variation in the st
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2.4 Neutron flux distribution One r
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etween the highest and the lowest v
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The isotope specific β eff values
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SESSION IV BASIC PHYSICS, MATERIALS
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1. Introduction Due to its excellen
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Figure 2. Tests scheme 0 340 h. 1 0
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Figure 4. Auger depth profile conce
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Figure 8. Auger depth profile conce
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deposited at the cold zone, and the
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inner layer grows inward from the o
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[8] V.M. Fedirko, O.I. Eliseeva, V.
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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
Page 618 and 619: Plutonium was simulated with the no
Page 620 and 621: The influence of uranium and pluton
Page 622 and 623: The influence of uranium and pluton
Page 624 and 625: REFERENCES [1] I.I. Nazarenko, A.M.
Page 626 and 627: 1. Introduction The long-term radio
Page 628 and 629: Ce Ce 3+ Cl - Cl 2 The voltammogram
Page 630 and 631: Figure 3. Chronopotentiograms for t
Page 632 and 633: Figure 4. Potentiometric titrations
Page 634 and 635: Experimental solubilization tests w
Page 636 and 637: [13] H. Flood T. Förland and K. Mo
Page 638 and 639: 1. Introduction The separation of l
Page 640 and 641: Figure 4. Synthesis of amides 11-15
Page 642 and 643: 1. Introduction Over the recent yea
Page 644 and 645: 2.3.2 Set-up We set up a single HFM
Page 646 and 647: lower flow rates, Am(III) would be
Page 649 and 650: THE POTENTIAL OF NANO- AND MICROPAR
Page 651 and 652: efficiently and stable. This can be
Page 653 and 654: Figure 1a. Zetapotential of NTA-mod
Page 655 and 656: Scheme 7. Magnetic silica particles
Page 657: [13] L.H. Delmau, N. Simon, M.J. Sc
Page 660 and 661: 1. Introduction 137 90 Extraction p
Page 662 and 663: Figure 3. Schematic drawing of the
Page 664 and 665: (24), 8-PhPO(OH)-O-COSAN (25), and
Page 666 and 667: REFERENCES [1] Kyrš M., +H PiQHN S
Page 670 and 671: These data show that fuel lifetime
Page 673 and 674: RECENT PROGRESSES ON PARTITIONING S
Page 675 and 676: hot tests (See Table2) was enough f
Page 677 and 678: trace amount of Am and Eu. The HBTM
Page 679 and 680: 6. Conclusion Declassification of t
Page 681: POSTER SESSION BASIC PHYSICS: NUCLE
Page 684 and 685: 1. Introduction Among the large num
Page 686 and 687: The simulation of the spallation pr
Page 688 and 689: Table 1. Parameters of the two coll
Page 690 and 691: Figure 4. Radial distribution of th
Page 692 and 693: 6. The neutron escape line The comm
Page 694 and 695: Figure 7. Neutron background at the
Page 697 and 698: RECENT CAPTURE CROSS-SECTIONS VALID
Page 699 and 700: Figure 1. The GENEPI accelerator an
Page 701 and 702: 2.3.3 Neutron flux measurements •
Page 703 and 704: Figure 6. Time spectrum of 3 He gas
Page 705 and 706: 4. Analysis 4.1 Background subtract
Page 707 and 708: Figure 11. ENDF/B-VI, JEF2.2 and JE
Page 709 and 710: DOUBLE DIFFERENTIAL CROSS-SECTION F
Page 711 and 712: 3. Conclusion Double differential c
Page 713 and 714: Figure 3. Preliminary results of do
Page 715 and 716: MEASUREMENTS OF PARTICULE EMISSION
Page 717 and 718: 2. Experimental set-up The experime
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4. Results Figure 3 presents neutro
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1. Introduction Intermediate-energy
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Table 1. Relative neutron-induced c
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elow about 70 MeV [24] , where σ n
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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
Page 783 and 784:
2. Burnable absorber for HYPER 2.1
Page 785 and 786:
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
Page 798 and 799:
Φ >1 MeV = 1.0 10 13 to 1.0 x 10 1
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3. Irradiation targets and irradiat
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e transmuted in BR2 hence remain va
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Table 6. Atom percent concentration
Page 806 and 807:
advantage, with respect to FRs, of
Page 809 and 810:
ENHANCEMENT OF ACTINIDE INCINERATIO
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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
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Figure 3. Neutron spectra averaged
Page 819 and 820:
containing FA with B 4 C cladding i
Page 821:
REFERENCES [1] ANSALDO Technical Re
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1. Introduction At present, there a
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target means a change in k and the
Page 828 and 829:
Following the normal procedure for
Page 830 and 831:
Acknowledgements This study has bee
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1. ADS description A conceptual des
Page 834 and 835:
Substitution of (9) into (8), and u
Page 836 and 837:
With the coupling LAHET + MCNP-DSP,
Page 838 and 839:
Figure 3. Comparison for 1 and 5 pu
Page 841 and 842:
MOLTEN SALTS AS POSSIBLE FUEL FLUID
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2. The fuel salt for MSB concept Ma
Page 845 and 846:
and minor actinides must be removed
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
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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
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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