Plutonium bearing oxide fuels for recycling in thermal reactors and fast breeder reactors

International Nuclear Information System (INIS)

Cunningham, G.W.

1977-01-01

Programs carried out in the past two decades have established the technical feasibility of using plutonium as a fuel material in both water-cooled power reactors and sodium-cooled fast breeder reactors. The problem facing the technical community is basically one of demonstrating plutonium fuel recycle under strict conditions of public safety, accountability, personnel exposure, waste management, transportation and diversion or theft which are still evolving. In this paper only technical and economic aspects of high volume production and the demonstration program required are discussed. This paper discusses the role of mixed oxide fuels in light water reactors and the objectives of the LMFBR required for continual growth of nuclear power during the next century. The results of studies showing the impact of using plutonium on uranium requirements, power costs, and the market share of nuclear power are presented. The influence of doubling time and the introduction date of LMFBRs on the benefits to be derived by its commercial use are discussed. Advanced fuel development programs scoped to meet future commerical LMFBR fuel requirements are described. Programs designed to provide the basic technology required for using plutonium fuels in a manner which will satisfy all requirements for public acceptance are described. Included are the high exposure plutonium fabrication development program centered around the High Performance Fuels Laboratory being built at the Hanford Engineering Development Laboratory and the program to confirm the technology required for the production of mixed oxide fuels for light water reactors which is being coordinated by Savannah River Laboratories

Physics of plutonium recycling: volume V. Plutonium recycling in fast reactors

International Nuclear Information System (INIS)

1996-01-01

As part of a programme proposed by the OECD/NEA Working Party on Physics of Plutonium Recycling (WPPR) to evaluate different scenarios for the use of plutonium, fast reactor physics benchmarks were developed. In this report, the multi-recycle performance of the metal-fuelled benchmark is evaluated. Benchmark results assess the reactor performance and toxicity behaviour in a closed nuclear fuel cycle for a parametric variation of the conversion ratio between 0.5 and 1.0. Results indicate that a fast burner reactor closed fuel cycle can be utilised to significantly reduce the radiotoxicity originating in the LWR cycle which would otherwise be destined for burial. (Author). tabs., figs., refs

Long-term logistic analysis of FBR introduction strategy: avoiding both uranium and plutonium shortage

International Nuclear Information System (INIS)

Suzuki, T.

1995-01-01

Despite comfortable predictions on short to mid-term uranium resources, there is still a concern about long-term availability of competitive uranium resources. In order to achieve substantial uranium saving, early introduction of Fast Breeder Reactor (FBR) is desirable. But it is also known that rapid introduction of FBR could result in plutonium storage. Will there be enough plutonium on a global scale to sustain fast FBR growth? is there any other way to save uranium resource? This paper concludes that multi-option strategies to achieve flexible long-term strategy to avoid both uranium and plutonium storage are desirable. (authors)

PLUTONIUM METALLIC FUELS FOR FAST REACTORS

Energy Technology Data Exchange (ETDEWEB)

STAN, MARIUS [Los Alamos National Laboratory; HECKER, SIEGFRIED S. [Los Alamos National Laboratory

2007-02-07

Early interest in metallic plutonium fuels for fast reactors led to much research on plutonium alloy systems including binary solid solutions with the addition of aluminum, gallium, or zirconium and low-melting eutectic alloys with iron and nickel or cobalt. There was also interest in ternaries of these elements with plutonium and cerium. The solid solution and eutectic alloys have most unusual properties, including negative thermal expansion in some solid-solution alloys and the highest viscosity known for liquid metals in the Pu-Fe system. Although metallic fuels have many potential advantages over ceramic fuels, the early attempts were unsuccessful because these fuels suffered from high swelling rates during burn up and high smearing densities. The liquid metal fuels experienced excessive corrosion. Subsequent work on higher-melting U-PuZr metallic fuels was much more promising. In light of the recent rebirth of interest in fast reactors, we review some of the key properties of the early fuels and discuss the challenges presented by the ternary alloys.

The plutonium utilization in thermal and fast reactor in Japan

International Nuclear Information System (INIS)

Amanuma, T.; Uematsu, K.

1977-01-01

The nuclear power development in Japan is rather extensive one, and the installed nuclear power capacity is expected to reach 49,000 MWe by 1985 and possibly to reach 170,000 MWe by 2000 according to a prediction. Currently istalled nuclear power is mainly based on Light Water type Reactor, and this trend is expected to persist for the time-being. The plutonium produced by LWR will be accumulated to 20 tons by 1985 and to more than 200 tons by 2000. If the produced plutonium will simply be stored, it will raise the economic pressure to utilities and the management and physical protection problems associated with plutonium storing. Therefore, it is not too wise simply to store plutonium in a locked vault. In Japan, there are three ways of solving these problems which are currently worked out. There is no doubt that the best solution is to use plutonium in fast reactors. To reach this goal, an Experimental Fast Reactor ''JOYO''has been constructed and it is waiting for criticality in very near future. A prototype fast breeder reactor ''MONJU'', which is designed for about 300 MWe, is nearing to the last stage of the design work. The start of its construction will take place in a few yesars. The domonstration fast breeder reactor will come next to ''MONJU'' and the large scale commercial use of fast breeder reactor is expected to start around 1995. To anwer the near-term need for plutonium utilization, two technologies, which are equally important to Japan, are currently developed. One is the recycle use of plutonium into LWR. This technology has long been jointly developed by research organizations and utilities. Some of fuel irradiation data are already obtained and the physics study has also been extensive. The application of this technology is expected to start about 1987. The other is to burn plutonium in an Advanced Thermal Reactor (D 2 O moderated, Boiling Water Cooled) which shows better characteristics of using plutonium. The 160 MWe ''Fugen'' is a prototype

Gastrointestinal absorption of plutonium and uranium in fed and fasted adult baboons and mice: application to humans

International Nuclear Information System (INIS)

Bhattacharyya, M.H.; Larsen, R.P.; Oldham, R.D.; Cohen, N.; Ralston, L.G.; Moretti, E.S.; Ayres, L.

1989-01-01

Gastrointestinal (GI) absorption values of plutonium and uranium were determined in fed and fasted adult baboons and mice. For both baboons and mice, the GI absorptions of plutonium and uranium were 10 to 20 times higher in 24 h fasted animals than in fed ones. For plutonium, GI absorption values in baboons were almost identical to those in mice for both fed and fasted conditions, and values for fed animals agreed with estimates for humans. For uranium, GI absorption values in fed and fasted baboons were 6 to 7 times higher than those in mice, and agreed well with those fed and fasted humans. For one baboon that was not given its morning meal, plutonium absorption 2 h after the start of the active phase was the same as that in the 24 h fasted animals. In contrast, for baboons that received a morning meal, plutonium absorption did not rise to the value of 24 h fasted baboons even 8 h after the meal. We conclude that GI absorption values for plutonium and uranium in adult baboons are good estimates of the values in humans and that the values for the fasted condition should be used to set standards for oral exposure of persons in the workplace. (author)

Plutonium recovery from spent reactor fuel by uranium displacement

Science.gov (United States)

Ackerman, J.P.

1992-03-17

A process is described for separating uranium values and transuranic values from fission products containing rare earth values when the values are contained together in a molten chloride salt electrolyte. A molten chloride salt electrolyte with a first ratio of plutonium chloride to uranium chloride is contacted with both a solid cathode and an anode having values of uranium and fission products including plutonium. A voltage is applied across the anode and cathode electrolytically to transfer uranium and plutonium from the anode to the electrolyte while uranium values in the electrolyte electrolytically deposit as uranium metal on the solid cathode in an amount equal to the uranium and plutonium transferred from the anode causing the electrolyte to have a second ratio of plutonium chloride to uranium chloride. Then the solid cathode with the uranium metal deposited thereon is removed and molten cadmium having uranium dissolved therein is brought into contact with the electrolyte resulting in chemical transfer of plutonium values from the electrolyte to the molten cadmium and transfer of uranium values from the molten cadmium to the electrolyte until the first ratio of plutonium chloride to uranium chloride is reestablished.

Plutonium recovery from spent reactor fuel by uranium displacement

International Nuclear Information System (INIS)

Ackerman, J.P.

1992-01-01

A process is described for separating uranium values and transuranic values from fission products containing rare earth values when the values are contained together in a molten chloride salt electrolyte. A molten chloride salt electrolyte with a first ratio of plutonium chloride to uranium chloride is contacted with both a solid cathode and an anode having values of uranium and fission products including plutonium. A voltage is applied across the anode and cathode electrolytically to transfer uranium and plutonium from the anode to the electrolyte while uranium values in the electrolyte electrolytically deposit as uranium metal on the solid cathode in an amount equal to the uranium and plutonium transferred from the anode causing the electrolyte to have a second ratio of plutonium chloride to uranium chloride. Then the solid cathode with the uranium metal deposited thereon is removed and molten cadmium having uranium dissolved therein is brought into contact with the electrolyte resulting in chemical transfer of plutonium values from the electrolyte to the molten cadmium and transfer of uranium values from the molten cadmium to the electrolyte until the first ratio of plutonium chloride to uranium chloride is reestablished

Plans for the development of the IFR [Integral Fast Reactor] fuel cycle

International Nuclear Information System (INIS)

Johnson, T.R.

1986-01-01

The Integral Fast Reactor (IFR) is a concept for a self-contained facility in which several sodium-cooled fast reactors of moderate size are located at the same site along with complete fuel-recycle and waste-treatment facilities. After the initial core loading with enriched uranium or plutonium, only natural or depleted uranium is shipped to the plant, and only wastes in final disposal forms are shipped out. The reactors have driver and blanket fuels of uranium-plutonium-zirconium alloys in stainless steel cladding. The use of metal alloy fuels is central to the IFR concept, contributing to the inherent safety of the reactor, the ease of reprocessing, and the relatively low capital and operating costs. Discharged fuels are recovered in a pyrochemical process that consists of two basic steps: an electrolytic process to separate fission products from actinides, and halide slagging to separate plutonium from uranium

The plutonium fuel cycles

International Nuclear Information System (INIS)

Pigford, T.H.; Ang, K.P.

1975-01-01

The quantities of plutonium and other fuel actinides have been calculated for equilibrium fuel cycles for 1000-MW water reactors fueled with slightly enriched uranium, water reactors fueled with plutonium and natural uranium, fast-breder reactors, gas-cooled reactors fueled with thorium and highly enriched uranium, and gas-cooled reactors fueled with thorium, plutonium and recycled uranium. The radioactivity quantities of plutonium, americium and curium processed yearly in these fuel cycles are greatest for the water reactors fueled with natural uranium and recycled plutonium. The total amount of actinides processed is calculated for the predicted future growth of the U.S. nuclear power industry. For the same total installed nuclear power capacity, the introduction of the plutonium breeder has little effect upon the total amount of plutonium in this century. The estimated amount of plutonium in the low-level process wastes in the plutonium fuel cycles is comparable to the amount of plutonium in the high-level fission product wastes. The amount of plutonium processed in the nuclear fuel cycles can be considerably reduced by using gas-cooled reactors to consume plutonium produced in uranium-fueled water reactors. These, and other reactors dedicated for plutonium utilization, could be co-located with facilities for fuel reprocessing ad fuel fabrication to eliminate the off-site transport of separated plutonium. (author)

Fuel Cycle Impacts of Uranium-Plutonium Co-extraction

International Nuclear Information System (INIS)

Taiwo, Temitope; Szakaly, Frank; Kim, Taek-Kyum; Hill, Robert

2008-01-01

A systematic investigation of the impacts of uranium and plutonium co-extraction during fuel separations on reactor performance and fuel cycle has been performed. Proliferation indicators, critical mass and radiation source levels of the separation products or fabricated fuel, were also evaluated. Using LWR-spent-uranium-based MOX fuel instead of natural-uranium-based fuel in a PWR MOX core requires a higher initial plutonium content (∼1%), and results in higher Np-237 content (factor of 5) in the spent fuel, and less consumption of Pu-238 (20%) and Am-241 (14%), indicating a reduction in the effective repository space utilization. Additionally, minor actinides continue to accumulate in the fuel cycle, and thus a separate solution is required for them. Differences were found to be quite smaller (∼0.4% in initial transuranics) between the equilibrium cycles of advanced fast reactor cores using spent and depleted uranium for make-up, in additional to transuranics. The critical masses of the co-extraction products were found to be higher than for weapons-grade plutonium (WG-Pu) and the decay heat and radiation sources of the materials (products) were also found to be generally higher than for WG-Pu in the transuranics content range of 10% to 100% in the heavy-metal. (authors)

Recent irradiation tests of uranium-plutonium-zirconium metal fuel elements

International Nuclear Information System (INIS)

Pahl, R.G.; Lahm, C.E.; Villarreal, R.; Hofman, G.L.; Beck, W.N.

1986-09-01

Uranium-Plutonium-Zirconium metal fuel irradiation tests to support the ANL Integral Fast Reactor concept are discussed. Satisfactory performance has been demonstrated to 2.9 at.% peak burnup in three alloys having 0, 8, and 19 wt % plutonium. Fuel swelling measurements at low burnup in alloys to 26 wt % plutonium show that fuel deformation is primarily radial in direction. Increasing the plutonium content in the fuel diminishes the rate of fuel-cladding gap closure and axial fuel column growth. Chemical redistribution occurs by 2.1 at.% peak burnup and generally involves the inward migration of zirconium and outward migration of uranium. Fission gas release to the plenum ranges from 46% to 56% in the alloys irradiated to 2.9 at.% peak burnup. No evidence of deleterious fuel-cladding chemical or mechanical interaction was observed

Astrid (fast breeder nuclear reactor)

International Nuclear Information System (INIS)

2014-01-01

This document presents ASTRID (Advanced Sodium Technological Reactor for Industrial Demonstration), a French project of sodium-cooled fast breeder reactor, fourth generation reactor which should be fuelled by uranium 238 rather than uranium 235, and should therefore need less extracted natural uranium to produce electricity. The operation principle of fast breeder reactors is described. They notably directly consume plutonium, allow an easier radioactive waste management as they transform long life radioactive elements into shorter life elements by transmutation. The regeneration process is briefly described, and the various operation modes are evoked (iso-generator, sub-generator, and breeder). Some peculiarities of sodium-cooled reactors are outlined. The Astrid operation principle is described, its main design innovations outlined. Various challenges are discussed regarding safety of supply and waste processing, and the safety of future reactors. Major actors are indicated: CEA, Areva, EDF, SEIV Alcen, Toshiba, Rolls Royce, and Comex. Some key data are indicated: expected lifetime, expected availability rate, cost. The projected site is Marcoule and fast breeder reactors operated or under construction in the world are indicated. The document also proposes an overview of the background and evolution of reactors of 4. generation

Destruction of plutonium using non-uranium fuels in pressurized water reactor peripheral assemblies

International Nuclear Information System (INIS)

Chodak, P. III

1996-05-01

This thesis examines and confirms the feasibility of using non-uranium fuel in a pressurized water reactor (PWR) radial blanket to eliminate plutonium of both weapons and civilian origin. In the equilibrium cycle, the periphery of the PWR is loaded with alternating fresh and once burned non-uranium fuel assemblies, with the interior of the core comprised of conventional three batch UO 2 assemblies. Plutonium throughput is such that there is no net plutonium production: production in the interior is offset by destruction in the periphery. Using this approach a 50 MT WGPu inventory could be eliminated in approximately 400 reactor years of operation. Assuming all other existing constraints were removed, the 72 operating US PWRs could disposition 50 MT of WGPu in 5.6 years. Use of a low fissile loading plutonium-erbium inert-oxide-matrix composition in the peripheral assemblies essentially destroys 100% of the 239 Pu and ≥90% total Pu over two 18 month fuel cycles. Core radial power peaking, reactivity vs EFPD profiles and core average reactivity coefficients were found to be comparable to standard PWR values. Hence, minimal impact on reload licensing is anticipated. Examination of potential candidate fuel matrices based on the existing experience base and thermo-physical properties resulted in the recommendation of three inert fuel matrix compositions for further study: zirconia, alumina and TRISO particle fuels. Objective metrics for quantifying the inherent proliferation resistance of plutonium host waste and fuel forms are proposed and were applied to compare the proposed spent WGPu non-uranium fuel to spent WGPu MOX fuels and WGPu borosilicate glass logs. The elimination disposition option spent non-uranium fuel product was found to present significantly greater barriers to proliferation than other plutonium disposal products

Destruction of plutonium using non-uranium fuels in pressurized water reactor peripheral assemblies

Energy Technology Data Exchange (ETDEWEB)

Chodak, III, Paul [Massachusetts Inst. of Technology (MIT), Cambridge, MA (United States)

1996-05-01

This thesis examines and confirms the feasibility of using non-uranium fuel in a pressurized water reactor (PWR) radial blanket to eliminate plutonium of both weapons and civilian origin. In the equilibrium cycle, the periphery of the PWR is loaded with alternating fresh and once burned non-uranium fuel assemblies, with the interior of the core comprised of conventional three batch UO₂ assemblies. Plutonium throughput is such that there is no net plutonium production: production in the interior is offset by destruction in the periphery. Using this approach a 50 MT WGPu inventory could be eliminated in approximately 400 reactor years of operation. Assuming all other existing constraints were removed, the 72 operating US PWRs could disposition 50 MT of WGPu in 5.6 years. Use of a low fissile loading plutonium-erbium inert-oxide-matrix composition in the peripheral assemblies essentially destroys 100% of the ²³⁹Pu and ≥90% {sub total}Pu over two 18 month fuel cycles. Core radial power peaking, reactivity vs EFPD profiles and core average reactivity coefficients were found to be comparable to standard PWR values. Hence, minimal impact on reload licensing is anticipated. Examination of potential candidate fuel matrices based on the existing experience base and thermo-physical properties resulted in the recommendation of three inert fuel matrix compositions for further study: zirconia, alumina and TRISO particle fuels. Objective metrics for quantifying the inherent proliferation resistance of plutonium host waste and fuel forms are proposed and were applied to compare the proposed spent WGPu non-uranium fuel to spent WGPu MOX fuels and WGPu borosilicate glass logs. The elimination disposition option spent non-uranium fuel product was found to present significantly greater barriers to proliferation than other plutonium disposal products.

Optimal reactor strategy for commercializing fast breeder reactors

International Nuclear Information System (INIS)

Yamaji, Kenji; Nagano, Koji

1988-01-01

In this paper, a fuel cycle optimization model developed for analyzing the condition of selecting fast breeder reactors in the optimal reactor strategy is described. By dividing the period of planning, 1966-2055, into nine ten-year periods, the model was formulated as a compact linear programming model. With the model, the best mix of reactor types as well as the optimal timing of reprocessing spent fuel from LWRs to minimize the total cost were found. The results of the analysis are summarized as follows. Fast breeder reactors could be introduced in the optimal strategy when they can economically compete with LWRs with 30 year storage of spent fuel. In order that fast breeder reactors monopolize the new reactor market after the achievement of their technical availability, their capital cost should be less than 0.9 times as much as that of LWRs. When a certain amount of reprocessing commitment is assumed, the condition of employing fast breeder reactors in the optimal strategy is mitigated. In the optimal strategy, reprocessing is done just to meet plutonium demand, and the storage of spent fuel is selected to adjust the mismatch of plutonium production and utilization. The price hike of uranium ore facilitates the commercial adoption of fast breeder reactors. (Kako, I.)

The integral fast reactor fuels reprocessing laboratory at Argonne National Laboratory, Illinois

International Nuclear Information System (INIS)

Wolson, R.D.; Tomczuk, Z.; Fischer, D.F.; Slawecki, M.A.; Miller, W.E.

1986-09-01

The processing of Integral Fast Reactor (IFR) metal fuel utilizes pyrochemical fuel reprocessing steps. These steps include separation of the fission products from uranium and plutonium by electrorefining in a fused salt, subsequent concentration of uranium and plutonium for reuse, removal, concentration, and packaging of the waste material. Approximately two years ago a facility became operational at Argonne National Laboratory-Illinois to establish the chemical feasibility of proposed reprocessing and consolidation processes. Sensitivity of the pyroprocessing melts to air oxidation necessitated operation in atmosphere-controlled enclosures. The Integral Fast Reactor Fuels Reprocessing Laboratory is described

Economical aspects of multiple plutonium and uranium recycling in VVER reactors

Energy Technology Data Exchange (ETDEWEB)

Alekseev, P.N.; Bobrov, E.A.; Dudnikov, A.A.; Teplov, P.S. [National Research Centre ' Kurchatov Institute' , Moscow (Russian Federation)

2016-09-15

The basic strategy of Russian Nuclear Energy development is the formation of the closed fuel cycle based on fast breeder and thermal reactors, as well as the solution of problems of spent nuclear fuel accumulation and availability of resources. Three options of multiple Pu and U recycling in VVER reactors are considered in this work. Comparison of MOX and REMIX fuel recycling approaches for the closed fuel cycle involving thermal reactors is presented. REMIX fuel is supposed to be fabricated from non-separated mixture of uranium and plutonium obtained in spent fuel reprocessing with further makeup by enriched U. These options make it possible to recycle several times the total amount of Pu and U obtained from spent fuel. The main difference is the full or partial fuel loading of the core by assemblies with recycled Pu. The third option presents the concept of heterogeneous arrangement of fuel pins made of enriched uranium and MOX in one fuel assembly. It should be noted that fabrication of all fuel assemblies with Pu requires the use of expensive manufacturing technology. These three options of core loading can be balanced with respect to maximum Pu and U involvement in the fuel cycle. Various physical and economical aspects of Pu and U multiple recycling for selected options are considered in this work.

Irradiation Experiments on Plutonium Fuels for Fast Reactors

Energy Technology Data Exchange (ETDEWEB)

Frost, B. R.T.; Wait, E. [Atomic Energy Research Establishment Harwell, Berks. (United Kingdom)

1967-09-15

experiment was conducted in a thermal neutron flux to a mean burn-up in excess of 10% burn-up but with a low fuel centre temperature (< 900 Degree-Sign C). Under these conditions gas release was low and fuel swelling was sufficiently low to avoid can failure, in contrast with other results at the same burn-up but at higher fuel centre temperatures ({approx} 1300 Degree-Sign C) where gas release and swelling were both considerably higher. Further experiments are in progress to determine more accurately the rate of swelling of (U, Pu)C in a fast neutron flux and to study possible methods of prolonging the life of carbide fuel elements. These studies are supported by basic investigations of swelling and fission gas release mechanisms. An assessment of the chemical state of the fuel fission products and cladding after irradiation to high burn-up is presented. The analysis is based on the thermodynamics of the system and experimental observations on irradiated fuel material. The systems considered are uranium/plutonium oxide and uranium/plutonium carbides. The principal conclusions of the analysis are that, in oxides, the oxygen potential of the system increases with increasing burn-up and, in carbides, the carbon activity of die irradiated system is maintained at some value between that of the monocarbide and sesquicarbide. (author)

Prospects for plutonium recycling in light-water reactors in the European Communities

International Nuclear Information System (INIS)

Haijtink, B.

1977-01-01

On the basis of a forecast on nuclear power installation programmes and spent nuclear fuel reprocessing capacities in the European Community, an assessment has been made of the developmnt of the plutonium handling industry up to the year 1990. Data on plutonium recovered in the reprocessing plants, requirements for fuelling the fast-breeder reactors and the remaining stockpile have been evaluated. A possible strategy for recycling the plutonium surplus in light-water reactors has been developed and its effects as regards saving on requirements for natural uranium and enrichment services have been estimated

Experience on Russian military origin plutonium conversion into fast reactor nuclear fuel

International Nuclear Information System (INIS)

Grachev, A.F.; Skiba, O.V.; Bychkov, A.V.; Mayorshin, A.A.; Kisly, V.A.; Bobrov, D.A.; Osipenko, A.G.; Babikov, L.G.; Mishinev, V.B.

2001-01-01

According to the Concept of Russian Minatom on military plutonium excess utilization, the State Scientific Center of Russian Federation ''Research Institute of Atomic Reactors'' (Dimitrovgrad) has begun study on possibility of technological processing of the metal military plutonium into MOX fuel. The Program and the stages of its realization are submitted in the paper. During 1998-2000 the first stage of the Program was fulfilled and 50 kg of military origin metallic plutonium was converted to MOX fuel for the BOR-60 and BN-600 reactor. The plutonium conversion into MOX fuel is carried out under the original technology developed by SSC RIAR. It includes pyro-electrochemical process for production of fuel on the domestic equipment with the subsequent fuel pins manufacturing for the fast reactors by the vibro-packing method. The produced MOX fuel is purified from alloy additives (Ga) and corresponds to the vibro-packed fuel standard for fast reactors. The fuel pins manufacturing for BOR-60 and BN-600 reactors are carried out by the vibro-packing method on a standard procedure, which is used in SSC RIAR more than 20 years. (author)

Partitioning of plutonium and uranium in aqueous medium using hydroxyurea as reducing agent

International Nuclear Information System (INIS)

Sivakumar, P.; Subba Rao, R.V.; Meenakshi, S.

2012-01-01

A new process for the partitioning of plutonium and uranium during the reprocessing of spent fuel discharged from fast reactor was optimised using hydroxyurea (HU) as a reductant. Stoichiometric ratio of HU required for the reduction of Pu(IV) was studied. The effect of concentration of uranium, plutonium and acidity on the distribution ratio (Kd) of Pu in the presence of HU was studied. The effect of HU in further purification of Pu such as solvent extraction and precipitation of plutonium as oxalate was also studied. The results of the study indicate that Pu and U can be separated from each other using HU as reductant. (author)

Uranium plutonium oxide fuels

International Nuclear Information System (INIS)

Cox, C.M.; Leggett, R.D.; Weber, E.T.

1981-01-01

Uranium plutonium oxide is the principal fuel material for liquid metal fast breeder reactors (LMFBR's) throughout the world. Development of this material has been a reasonably straightforward evolution from the UO 2 used routinely in the light water reactor (LWR's); but, because of the lower neutron capture cross sections and much lower coolant pressures in the sodium cooled LMFBR's, the fuel is operated to much higher discharge exposures than that of a LWR. A typical LMFBR fuel assembly is shown. Depending on the required power output and the configuration of the reactor, some 70 to 400 such fuel assemblies are clustered to form the core. There is a wide variation in cross section and length of the assemblies where the increasing size reflects a chronological increase in plant size and power output as well as considerations of decreasing the net fuel cycle cost. Design and performance characteristics are described

Transmutation of plutonium in pebble bed type high temperature reactors

International Nuclear Information System (INIS)

Bende, E.E.

1997-01-01

The pebble bed type High Temperature Reactor (HTR) has been studied as a uranium-free burner of reactor grade plutonium. In a parametric study, the plutonium loading per pebble as well as the type and size of the coated particles (CPs) have been varied to determine the plutonium consumption, the final plutonium burnup, the k ∞ and the temperature coefficients as a function of burnup. The plutonium loading per pebble is bounded between 1 and 3 gr Pu per pebble. The upper limit is imposed by the maximal allowable fast fluence for the CPs. A higher plutonium loading requires a longer irradiation time to reach a desired burnup, so that the CPs are exposed to a higher fast fluence. The lower limit is determined by the temperature coefficients, which become less negative with increasing moderator-actinide ratio. A burnup of about 600 MWd/kgHM can be reached. With the HTR's high efficiency of 40%, a plutonium supply of 1520 kg/GW e a is achieved. The discharges of plutonium and minor actinides are then 450 and 110 kg/GW e a, respectively. (author)

Weapons-grade plutonium dispositioning. Volume 3: A new reactor concept without uranium or thorium for burning weapons-grade plutonium

International Nuclear Information System (INIS)

Ryskamp, J.M.; Schnitzler, B.G.; Fletcher, C.D.

1993-06-01

The National Academy of Sciences (NAS) requested that the Idaho National Engineering Laboratory (INEL) examine concepts that focus only on the destruction of 50,000 kg of weapons-grade plutonium. A concept has been developed by the INEL for a low-temperature, low-pressure, low-power density, low-coolant-flow-rate light water reactor that destroys plutonium quickly without using uranium or thorium. This concept is very safe and could be designed, constructed, and operated in a reasonable time frame. This concept does not produce electricity. Not considering other missions frees the design from the paradigms and constraints used by proponents of other dispositioning concepts. The plutonium destruction design goal is most easily achievable with a large, moderate power reactor that operates at a significantly lower thermal power density than is appropriate for reactors with multiple design goals. This volume presents the assumptions and requirements, a reactor concept overview, and a list of recommendations. The appendices contain detailed discussions on plutonium dispositioning, self-protection, fuel types, neutronics, thermal hydraulics, off-site radiation releases, and economics

The fast breeder reactor

International Nuclear Information System (INIS)

Patterson, W.

1990-01-01

The author criticises the United Kingdom Atomic Energy Authority's fast breeder reactor programme in his evidence to the House of Commons Select Committee on Energy in January 1990. He argues for power generation by renewable means and greater efficiency in the use rather than in the generation of electricity. He refutes the arguments for nuclear power on the basis of reduced global warming as he claims support technology produces significant amounts of carbon dioxide in any case. Serious doubts are raised about the costs of a fast breeder reactor programme compared to, say, generation by pressurised water reactors. The idea of a uranium scarcity in several decades is also refuted. The reliability of fast breeder reactor technology is called into question. He argues against reprocessing plutonium for economic, health and safety reasons. (UK)

Logistical and economic obstacles to a fast reactor programme

International Nuclear Information System (INIS)

Sweet, C.

1982-01-01

Fast reactor studies used to place great emphasis on its role as a breeder of plutonium, thereby raising the prospect of a nuclear power system free from the constraint of uranium supplies. Today, not only the timing of fast reactor introduction has slipped (by two or three decades) but the perspective which was central to energy policy has changed dramatically. This article first examines the fast reactor as a system and looks at the interaction of four key variables in its logistics. It then looks at the rise in real costs, especially capital costs. Given the parameters that determine the plutonium balance and the economics of the fast reactor system, the author questions whether there is a sound basis for its introduction, and concludes by suggesting that the most pressing requirement is a study of the opportunity costs of fast reactor R and D expenditures. (author)

History of fast reactor fuel development

Energy Technology Data Exchange (ETDEWEB)

Kittel, J.H. (Argonne National Lab., IL (United States)); Frost, B.R.T. (Argonne National Lab., IL (United States)); Mustelier, J.P. (COGEMA, Velizy-Villacoublay (France)); Bagley, K.Q. (AEA Reactor Services, Risley (United Kingdom)); Crittenden, G.C. (AEA Reactor Services, Dounreay (United Kingdom)); Dievoet, J. van (Belgonucleaire, Brussels (Belgium))

1993-09-01

The first fast breeder eactors, constructed in the 1945-1960 time period, used metallic fuels composed of uranium, plutonium, or their alloys. They were chosen because most existing reactor operating experience had been obtained on metallic fuels and because they provided the highest breeding ratios. Difficulties in obtaining adequate dimensional stability in metallic fuel elements under conditions of high fuel burnup led in the 1960s to the virtual worldwide choice of ceramic fuels. Although ceramic fuels provide lower breeding performance, this objective is no longer an important consideration in most national programs. Mixed uranium and plutonium dioxide became the ceramic fuel that has received the widest use. The more advanced ceramic fuels, mixed uranium and plutonium carbides and nitrides, continue under development. More recently, metal fuel elements of improved design have joined ceramic fuels in achieving goal burnups of 15 to 20 percent. Low-swelling fuel cladding alloys have also been continuously developed to deal with the unexpected problem of void formation in stainless steels subjected to fast neutron irradiation, a phenomenon first observed in the 1960s. (orig.)

Simulation study for purification, recovery of plutonium and uranium from plant streams of Fast Reactor Fuel Reprocessing Plant

International Nuclear Information System (INIS)

Sukumar, S.; Siva Kumar, P.; Radhika, R.; Subbuthai, S.; Mohan, S.V.; Subha Rao, R.V.

2005-01-01

A method for removal of plutonium from the lean organic streams obtained after co-stripping of uranium -plutonium was developed. Plutonium from lean organic phase was stripped using U 4+ /hydrazine as the stripping agent. The effect of concentrations of stripping agent U 4+ and feed Pu concentration in the lean organic phase was studied. Lean organic phases having higher plutonium concentration require three stages of stripping to bring plutonium concentration 4+ stabilized by hydrazine reduces Pu (IV) to Pu (III) thereby stripping plutonium from the organic phase. The non-extractability of Pu (III) by TBP was utilized for development of flow sheet for obtaining a uranium product lean of plutonium for ease of handling. (author)

The development of fast reactors - Effects on the Swedish system of management of spent fuel; Utveckling av snabba reaktorer - Paaverkan paa det svenska systemet foer hantering av anvaent braensle

Energy Technology Data Exchange (ETDEWEB)

Hans Forsstroem, Hans [SKB International AB, Stockholm (Sweden)

2013-09-15

Since the start of the nuclear power era studies have been performed of how to utilise the uranium energy resource in the most effective way. Only about one percent of the energy potential of uranium is utilised in the light water reactors of today. To improve the utilization other types of reactors are needed. With fast reactors theoretically 50-100 times more energy can be extracted from the uranium. This will require reprocessing of the uranium and multiple recycling of the plutonium. Plutonium and uranium can also be recycled in light water reactors, but this will only improve the uranium utilisation by about 20 %. Recycling of plutonium on a routine basis is presently only done in France. The development of fast reactors has been going on since the end of the 1940ies. During the 1970ies the planning was that a large number of fast reactors and their associated fuel cycle facilities would be in operation by the year 2000. The development has, however, for different reasons been much slower than planned. The general assessment today is that fast reactor, if they will be realised, will hardly give an important contribution to energy production until after 2050. Nuclear power production has instead been dominated by light water reactors similar to the ones in use in Sweden. Light water reactors are believed to continue to dominate during the next decades. To start a fast reactor system plutonium (or highly enriched uranium) will be needed. Such plutonium is contained in spent nuclear fuel from light water reactors. This raises the question: Should the spent nuclear fuel be stored so that the potential energy resource in the fuel can be used in the future instead of disposing of it as a waste? The answer to this question will depend on when the material will be useful, i.e. when fast reactors have been introduced on a large scale. It will also depend on the demand for plutonium at this time, i.e. will plutonium be a scarce redundant resource at this point of time

Study of plutonium recycling physics in light water reactors

International Nuclear Information System (INIS)

Reuss, Paul

1979-10-01

A stock of plutonium from the reprocessing of thermal neutron reactor fuel is likely to appear in the next few years. The use of this plutonium as fuel replacing 235 U in thermal reactors is probably more interesting than simple stock-piling storage: immobilization of a capital which moreover would deteriorate by radioactive decay of isotope 241 also fissile and present to an appreciable extend in plutonium from reprocessing (half-life 15 years); recycling, on the other hand, will supply energy without complete degradation of the stock for fast neutron reactor loads, the burned matter having been partially renewed by conversion; furthermore the use of plutonium will meet the needs created by a temporary pressure on the naturel and/or enriched uranium market. For these two reasons the recycling of plutonium in thermal neutron reactors is being considered seriously today. The present work is confined to neutronic aspects and centres mainly on pressurized water-moderated reactors, the most highly developed at present in France. Four aspects of the problem are examined: 1. the physics of a plutonium-recycling reactor special features of neutronic phenomena with respect to the 'conventional' scheme of the 235 U burning reactor; 2. calculation of a plutonium-recycling reactor: adaptation of standard methods; 3. qualification of these calculations from the viewpoint of both data and inevitable approximations; 4. the fuel cycle and particularly the equivalence of fissile matters [fr

Prospects for the Use of Plutonium in Reactors; Prospective d'Utilisation du Plutonium dans les Reacteurs

Energy Technology Data Exchange (ETDEWEB)

Fossoul, E.; Haubert, P. [BELGONUCLEAIRE (Belgium); Hirschberg, D.; Morlet, E. [International Business Machines of Belgium, Bruxelles (Belgium)

1967-09-15

The introduction, at an increasing rate, of power reactors using slightly enriched uranium will inevitably lead to the production of considerable quantities of plutonium over the next decade. Fast reactors will not be capable of absorbing this material before 1980. The question thus arises of whether one should store the plutonium far future use in fast reactors, recycle it in existing thermal reactors, or try to sell it. The problem has been studied for an electric power generating system that does not foresee selling the plutonium produced by its reactors and does not buy plutonium outside, which enables a good approximation to be made and eliminates the major unknown quantity represented by the future market price of plutonium. Assuming within this system a programme that provides for the construction of power reactors of a given type and capacity at specific dates, the utilization of the plutonium produced can be optimized by linear programming techniques so as to minimize the discounted total cost of the power generated over a given period. A later stage consists in optimizing, by various techniques, not only the utilization but also the production of plutonium by appropriate selection of the power reactor types to be constructed. (author) [French] L'implantation, a un rythme croissant, de centrales nucleaires a uranium legerement enrichi entrainera la production ineluctable d'une quantite importante de plutonium au cours de la prochaine decennie. Les reacteurs a neutrons rapides ne seront capables d'absorber cette production qu'apres 1980. La question se pose donc de savoir s'il est preferable de stocker le plutonium en vue de son utilisation ulterieure dans les reacteurs a neutrons rapides plutot que de le recycler dans les reacteurs actuels a neutrons thermiques ou d'essayer de le vendre. Ce probleme a ete etudie dans le cadre d'un systeme de production d'energie electrique qui ne prevoirait pas la vente du plutonium produit par ses reacteurs nucleaires ni

Profileration-proof uranium/plutonium and thorium/uranium fuel cycles. Safeguards and non-profileration. 2. rev. ed.

Energy Technology Data Exchange (ETDEWEB)

Kessler, G.

2017-07-01

A brief outline of the historical development of the proliferation problem is followed by a description of the uranium-plutonium nuclear fuel cycle with uranium enrichment, fuel fabrication, the light-water reactors mainly in operation, and the breeder reactors still under development. The next item discussed is reprocessing of spent fuel with plutonium recycling and the future possibility to incinerate plutonium and the minor actinides: neptunium, americium, and curium. Much attention is devoted to the technical and scientific treatment of the IAEA surveillance concept of the uranium-plutonium fuel cycle. In this context, especially the physically possible accuracy of measuring U/Pu flow in the fuel cycle, and the criticism expressed of the accuracy in measuring the plutonium balance in large reprocessing plants of non-nuclear weapon states are analyzed. The second part of the book initially examines the assertion that reactor-grade plutonium could be used to build nuclear weapons whose explosive yield cannot be predicted accurately, but whose minimum explosive yield is still far above that of chemical explosive charges. Methods employed in reactor physics are used to show that such hypothetical nuclear explosive devices (HNEDs) would attain too high temperatures in the required implosion lenses as a result of the heat generated by the Pu-238 isotope always present in reactor plutonium of current light-water reactors. These lenses would either melt or tend to undergo chemical auto-explosion. Limits to the content of the Pu-238 isotope are determined above which such hypothetical nuclear weapons are not feasible on technical grounds. This situation is analyzed for various possibilities of the technical state of the art of making implosion lenses and various ways of cooling up to the use of liquid helium. The outcome is that, depending on the existing state of the art, reactor-grade plutonium from spent fuel elements of light-water reactors with a burnup of 35 to 58

Survey of Worldwide Light Water Reactor Experience with Mixed Uranium-Plutonium Oxide Fuel

Energy Technology Data Exchange (ETDEWEB)

Cowell, B.S.; Fisher, S.E.

1999-02-01

The US and the Former Soviet Union (FSU) have recently declared quantities of weapons materials, including weapons-grade (WG) plutonium, excess to strategic requirements. One of the leading candidates for the disposition of excess WG plutonium is irradiation in light water reactors (LWRs) as mixed uranium-plutonium oxide (MOX) fuel. A description of the MOX fuel fabrication techniques in worldwide use is presented. A comprehensive examination of the domestic MOX experience in US reactors obtained during the 1960s, 1970s, and early 1980s is also presented. This experience is described by manufacturer and is also categorized by the reactor facility that irradiated the MOX fuel. A limited summary of the international experience with MOX fuels is also presented. A review of MOX fuel and its performance is conducted in view of the special considerations associated with the disposition of WG plutonium. Based on the available information, it appears that adoption of foreign commercial MOX technology from one of the successful MOX fuel vendors will minimize the technical risks to the overall mission. The conclusion is made that the existing MOX fuel experience base suggests that disposition of excess weapons plutonium through irradiation in LWRs is a technically attractive option.

Survey of Worldwide Light Water Reactor Experience with Mixed Uranium-Plutonium Oxide Fuel

International Nuclear Information System (INIS)

Cowell, B.S.; Fisher, S.E.

1999-01-01

The US and the Former Soviet Union (FSU) have recently declared quantities of weapons materials, including weapons-grade (WG) plutonium, excess to strategic requirements. One of the leading candidates for the disposition of excess WG plutonium is irradiation in light water reactors (LWRs) as mixed uranium-plutonium oxide (MOX) fuel. A description of the MOX fuel fabrication techniques in worldwide use is presented. A comprehensive examination of the domestic MOX experience in US reactors obtained during the 1960s, 1970s, and early 1980s is also presented. This experience is described by manufacturer and is also categorized by the reactor facility that irradiated the MOX fuel. A limited summary of the international experience with MOX fuels is also presented. A review of MOX fuel and its performance is conducted in view of the special considerations associated with the disposition of WG plutonium. Based on the available information, it appears that adoption of foreign commercial MOX technology from one of the successful MOX fuel vendors will minimize the technical risks to the overall mission. The conclusion is made that the existing MOX fuel experience base suggests that disposition of excess weapons plutonium through irradiation in LWRs is a technically attractive option

Integral test of JENDL-3.3 for fast reactors

International Nuclear Information System (INIS)

Chiba, Gou

2003-01-01

An integral test of JENDL-3.3 was performed for fast reactors. Various types of fast reactors were analyzed. Calculation values of the nuclear characteristics were greatly especially affected by the revisions of the cross sections of U-235 capture and elastic scattering reactions. The C/E values were improved for ZPPR cross where plutonium is mainly fueled, but not for BFS cores where uranium is mainly fueled. (author)

Comparative assessment of nuclear fuel cycles. Light-water reactor once-through, classical fast breeder reactor, and symbiotic fast breeder reactor cycles

International Nuclear Information System (INIS)

Hardie, R.W.; Barrett, R.J.; Freiwald, J.G.

1980-06-01

The object of the Alternative Nuclear Fuel Cycle Study is to perform comparative assessments of nuclear power systems. There are two important features of this study. First, this evaluation attempts to encompass the complete, integrated fuel cycle from mining of uranium ore to disposal of waste rather than isolated components. Second, it compares several aspects of each cycle - energy use, economics, technological status, proliferation, public safety, and commercial potential - instead of concentrating on one or two assessment areas. This report presents assessment results for three fuel cycles. These are the light-water reactor once-through cycle, the fast breeder reactor on the classical plutonium cycle, and the fast breeder reactor on a symbiotic cycle using plutonium and 233 U as fissile fuels. The report also contains a description of the methodology used in this assessment. Subsequent reports will present results for additional fuel cycles

Plutonium in depleted uranium penetrators

International Nuclear Information System (INIS)

McLaughlin, J.P.; Leon-Vintro, L.; Smith, K.; Mitchell, P.I.; Zunic, Z.S.

2002-01-01

Depleted Uranium (DU) penetrators used in the recent Balkan conflicts have been found to be contaminated with trace amounts of transuranic materials such as plutonium. This contamination is usually a consequence of DU fabrication being carried out in facilities also using uranium recycled from spent military and civilian nuclear reactor fuel. Specific activities of 239+240 Plutonium generally in the range 1 to 12 Bq/kg have been found to be present in DU penetrators recovered from the attack sites of the 1999 NATO bombardment of Kosovo. A DU penetrator recovered from a May 1999 attack site at Bratoselce in southern Serbia and analysed by University College Dublin was found to contain 43.7 +/- 1.9 Bq/kg of 239+240 Plutonium. This analysis is described. An account is also given of the general population radiation dose implications arising from both the DU itself and from the presence of plutonium in the penetrators. According to current dosimetric models, in all scenarios considered likely ,the dose from the plutonium is estimated to be much smaller than that due to the uranium isotopes present in the penetrators. (author)

The benefits of an advanced fast reactor fuel cycle for plutonium management

International Nuclear Information System (INIS)

Hannum, W.H.; McFarlane, H.F.; Wade, D.C.; Hill, R.N.

1996-01-01

The United States has no program to investigate advanced nuclear fuel cycles for the large-scale consumption of plutonium from military and civilian sources. The official U.S. position has been to focus on means to bury spent nuclear fuel from civilian reactors and to achieve the spent fuel standard for excess separated plutonium, which is considered by policy makers to be an urgent international priority. Recently, the National Research Council published a long awaited report on its study of potential separation and transmutation technologies (STATS), which concluded that in the nuclear energy phase-out scenario that they evaluated, transmutation of plutonium and long-lived radioisotopes would not be worth the cost. However, at the American Nuclear Society Annual Meeting in June, 1996, the STATS panelists endorsed further study of partitioning to achieve superior waste forms for burial, and suggested that any further consideration of transmutation should be in the context of energy production, not of waste management. 2048 The U.S. Department of Energy (DOE) has an active program for the short-term disposition of excess fissile material and a 'focus area' for safe, secure stabilization, storage and disposition of plutonium, but has no current programs for fast reactor development. Nevertheless, sufficient data exist to identify the potential advantages of an advanced fast reactor metallic fuel cycle for the long-term management of plutonium. Advantages are discussed

Review of fast reactor activities in India (1983-84)

International Nuclear Information System (INIS)

Paranjpe, S.R.

1984-01-01

The last year was very significant for the Indian Nuclear Energy Programme as the first indigeneously built heavy water moderated natural uranium reactor called Madras Atomic Power Plant Unit-I was made operational and connected to the grid. The power level has been gradually increased and the reactor has been operating at a power level of 200 MWe (temporarily limited by Plutonium build up during approach to equilibrium core loading). The 'plutonium peak' will be crossed shortly clearing the way for raising the reactor to the full power of 235 MWe gross. The second unit of MAPP, is well advanced and barring unforeseen difficulties, is expected to become operational during this financial year. This has been a big morale booster for the programme in general and the Fast Reactor Programme in particular as plutonium produced in these reactors is expected to be the inventory for Prototype Fast Breeder Reactors. It may be recalled that in the last report to this group, a reference was made to initiation of some preliminary design studies for such a reactor

Plutonium

International Nuclear Information System (INIS)

Watson, G.M.

1976-01-01

Discovery of the neutron made it easy to create elements which do not exist in nature. One of these is plutonium, and its isotope with mass number 239 has nuclear properties which make it both a good fuel for nuclear power reactors and a good explosive for nuclear weapons. Since it was discovered during a war the latter characteristic was put to use, but it is now evident that use of plutonium in a particular kind of nuclear reactor, the fast breeder reactor, will allow the world's resources of uranium to last for millennia as a major source of energy. Plutonium is very radiotoxic, resembling radium in this respect. Therefore the widespread introduction of fast breeder reactors to meet energy demands can be contemplated only after assurances on two points; that adequate control of the radiological hazard resulting from the handling of very large amounts of plutonium can be guaranteed, and that diversion of plutonium to illicit use can be prevented. The problems exist to a lesser degree already, since all types of nuclear reactor produce some plutonium. Some plutonium has already been dispersed in the environment, the bulk of it from atmospheric tests of nuclear weapons. (author)

Plutonium in uranium deposits

International Nuclear Information System (INIS)

Curtis, D.; Fabryka-Martin, J.; Aguilar, R.; Attrep, M. Jr.; Roensch, F.

1992-01-01

Plutonium-239 (t 1/2 , 24,100 yr) is one of the most persistent radioactive constituents of high-level wastes from nuclear fission power reactors. Effective containment of such a long-lived constituent will rely heavily upon its containment by the geologic environment of a repository. Uranium ore deposits offer a means to evaluate the geochemical properties of plutonium under natural conditions. In this paper, analyses of natural plutonium in several ores are compared to calculated plutonium production rates in order to evaluate the degree of retention of plutonium by the ore. The authors find that current methods for estimating production rates are neither sufficiently accurate nor precise to provide unambiguous measures of plutonium retention. However, alternative methods for evaluating plutonium mobility are being investigated, including its measurement in natural ground waters. Preliminary results are reported and establish the foundation for a comprehensive characterization of plutonium geochemistry in other natural environments

[Present conceptions of the C.E.A. concerning] the development of fast neutron reactors in France

International Nuclear Information System (INIS)

Vendryes, G.; Gaussens, J.

1964-01-01

1 - The position of fast neutron reactors in the French nuclear energy program. In developing a program based on natural uranium, France will have an important stock of plutonium rich in higher isotopes. The existence of this plutonium and of the depleted uranium arising from the same reactors, has, as a logical consequence, the use of both in fast neutron reactors. Justified by this short term interest, the achievement of fast neutron reactors does, moreover, provide for a future necessity. 2 - Description of a fast neutron central power station of 1000 MWe. We indicate the characteristics of a future fast neutron central power station, plutonium fuelled, and sodium cooled. However uncertain these characteristics may be, they constitute a necessary guide in the orientation of our work. 3 - Studies carried out up to the present time. We give an outline of those studies, often very preliminary, which have given the characteristics cited above. The principal technical areas taken up are the following: - Neutronics (critical masses, breeding ratios, enrichments, flattening of the neutron flux, coefficients of reactivity, reactivity changes as a function of irradiation). - Dynamics, control, and safety. - Technology (design of the core and vessel, of the sodium system, and of the fuel handling mechanisms). These technical studies are complemented by economic considerations. The choice of the optimum characteristics is related to the existence of power production programs, and, in these programs, to the existence of plutonium producing thermal reactors. It is shown how, in this context, the existence of plutonium should be taken into account, and, in addition which mechanisms relate the economics of this plutonium to the choice of the most important parameters of the breeder reactors. 4 - Prototype reactor. The interest in an intermediate stage consisting of a reactor of a power level of about 80 MWe is justified. Its essential characteristics are briefly presented

Fast reactor fuel reprocessing. An Indian perspective

International Nuclear Information System (INIS)

Natarajan, R.; Raj, Baldev

2005-01-01

The Department of Atomic Energy (DAE) envisioned the introduction of Plutonium fuelled fast reactors as the intermediate stage, between Pressurized Heavy Water Reactors and Thorium-Uranium-233 based reactors for the Indian Nuclear Power Programme. This necessitated the closing of the fast reactor fuel cycle with Plutonium rich fuel. Aiming to develop a Fast Reactor Fuel Reprocessing (FRFR) technology with low out of pile inventory, the DAE, with over four decades of operating experience in Thermal Reactor Fuel Reprocessing (TRFR), had set up at the India Gandhi Center for Atomic Research (IGCAR), Kalpakkam, R and D facilities for fast reactor fuel reprocessing. After two decades of R and D in all the facets, a Pilot Plant for demonstrating FRFR had been set up for reprocessing the FBTR (Fast Breeder Test Reactor) spent mixed carbide fuel. Recently in this plant, mixed carbide fuel with 100 GWd/t burnup fuel with short cooling period had been successfully reprocessed for the first time in the world. All the challenging problems encountered had been successfully overcome. This experience helped in fine tuning the designs of various equipments and processes for the future plants which are under construction and design, namely, the DFRP (Demonstration Fast reactor fuel Reprocessing Plant) and the FRP (Fast reactor fuel Reprocessing Plant). In this paper, a comprehensive review of the experiences in reprocessing the fast reactor fuel of different burnup is presented. Also a brief account of the various developmental activities and strategies for the DFRP and FRP are given. (author)

Fast burner reactor benchmark results from the NEA working party on physics of plutonium recycle

International Nuclear Information System (INIS)

Hill, R.N.; Wade, D.C.; Palmiotti, G.

1995-01-01

As part of a program proposed by the OECD/NEA Working Party on Physics of Plutonium Recycling (WPPR) to evaluate different scenarios for the use of plutonium, fast reactor physics benchmarks were developed; fuel cycle scenarios using either PUREX/TRUEX (oxide fuel) or pyrometallurgical (metal fuel) separation technologies were specified. These benchmarks were designed to evaluate the nuclear performance and radiotoxicity impact of a transuranic-burning fast reactor system. International benchmark results are summarized in this paper; and key conclusions are highlighted

R and D on fast reactor fuel reprocessing

International Nuclear Information System (INIS)

Subba Rao, R.V.; Vijaya Kumar, V.; Natarajan, R.

2012-01-01

Development of Fast Reactor Fuel Reprocessing technology, with low out of pile inventory, is carried out at the Indira Gandhi Centre for Atomic Research (IGCAR). Based on the successful R and D programme which addressed specific issues of fast reactor fuels, a pilot plant called CORAL was set up. This plant is operational since 2003 and several reprocessing campaigns with spent FBTR fuels of varying burnups have been carried out. Based on the valuable operating experience of CORAL, the design of demonstration fast reactor fuel reprocessing plant (DFRP) and the commercial reprocessing plant, FRP have been taken up. Concurrently R and D efforts are continuing for improving the process and equipment performance apart from reducing the waste volumes and the radiation exposures to the operating personnel. Some important R and D efforts are highlighted in the paper. Reducing the dissolution time is one of the vital area of investigation especially for the high plutonium bearing MOX fuels which are known to dissolve slowly. To address this as well as criticality issues, continuous dissolvers are being developed. Solvent extraction based process is employed for getting highly pure nuclear grade uranium and plutonium. In view of the lower cooling time the fission product activity in the spent fuel is higher, formulation of process flowsheet with reduced number of solvent extraction cycles to improve the decontamination of ruthenium and zirconium without the formation of second organic phase due to plutonium loading, is under investigation. Retention of plutonium in lean organic is another issue to be addressed as otherwise it would lead to further deterioration of the solvent on storage. Several reagents to effectively wash the lean solvent have been investigated and flowsheets have been formulated to recover the retained plutonium with minimum secondary wastes. Partitioning of uranium and plutonium is an important step and methods reported in the literature have inherent

Trans-Uranium Doping Utilization for Increasing Protected Plutonium Proliferation of Small Long Life Reactor

Energy Technology Data Exchange (ETDEWEB)

Permana, Sidik [Research Laboratory for Nuclear Reactors, Tokyo Institute of Technology 2-12-1-N1-17, O-okayama, Meguro-ku, Tokyo 152-8550 (Japan); Nuclear and Biophysics Research Group, Department of Physics, Bandung Institute of Technology, Gedung Fisika, Jl. Ganesha 10, Bandung 40132 (Indonesia); Suud, Zaki [Nuclear and Biophysics Research Group, Department of Physics, Bandung Institute of Technology, Gedung Fisika, Jl. Ganesha 10, Bandung 40132 (Indonesia); Suzuki, Mitsutoshi [Japan Atomic Energy Agency, Nuclear Non-proliferation Science and Technology Center, 2-4 Shirane Shirakata, Tokai-mura, Ibaraki, 319-1195 (Japan)

2009-06-15

Scientific approaches are performed by adopting some methodologies in order to increase a material 'barrier' in plutonium isotope composition by increasing the even mass number of plutonium isotope such as Pu-238, Pu-240 and Pu-242. Higher difficulties (barrier) or more complex requirement for peaceful use of nuclear materials, material fabrication and handling and isotopic enrichment can be achieved by a higher isotopic barrier. Higher barrier which related to intrinsic properties of plutonium isotopes with even mass number (Pu-238, Pu-240 and Pu-242), in regard to their intense decay heat (DH) and high spontaneous fission neutron (SFN) rates were used as a parameter for improving the proliferation resistance of plutonium itself. Pu-238 has relatively high intrinsic characteristics of DH (567 W/kg) and SFN rate of 2660 n/g/s can be used for making a plutonium characteristics analysis. Similar characteristics with Pu-238, other even mass number of plutonium isotopes such as Pu-240 and Pu-242 have been shown in regard to SFN values. Those even number mass of plutonium isotope contribute to some criteria of plutonium characterization which will be adopted for present study such as IAEA, Pellaud and Kessler criteria (IAEA, 1972; Pellaud, 2002; and Kessler, 2004). The study intends to evaluate the trans-uranium doping effect for increasing protected plutonium proliferation in long-life small reactors. The development of small and medium reactor (SMR) is one of the options which have been adopted by IAEA as future utilization of nuclear energy especially for less developed countries (Kuznetsov, 2008). The preferable feature for small reactors (SMR) is long life operation time without on-site refueling and in the same time, it includes high proliferation resistance feature. The reactor uses MOX fuel as driver fuel for two different core types (inner and outer core) with blanket fuel arrangement. Several trans-uranium doping and some doping rates are evaluated

Stability with temperature of mixed uranium plutonium monocarbides

International Nuclear Information System (INIS)

Riglet-Martial, Ch.; Dumas, J.C.; Piron, J.P.; Gueneau, Ch.

2008-01-01

Full text: Among the different advanced fuel materials of concern for Generation IV systems, the mixed carbide of uranium and plutonium fuel is considered as one of the key materials for Gas Fast Reactors (GFR) systems. For purposes of optimising its fabrication process as well as its performances in various operating conditions, the losses of gaseous plutonium specially at elevated temperatures have to be controlled and minimized. The paper is therefore concerned with a parametric analysis of the stability with temperature of mixed carbides of uranium and plutonium. Previous published experimental studies have shown that mixed (U ,Pu) carbides undergo a highly incongruent sublimation at high temperatures: the vapour phase in equilibrium with the solid is mainly composed of gaseous plutonium (P Pu /P total > 99 % ) while the contribution of gaseous U and C remains very low. The composition of the system U 1-z Pu z C 1+x ' (z =Pu/(U+Pu) and x C/(U+Pu)), the temperature (T) and the expansion volume (V) of the gas are the main parameters in the loss of gaseous Pu. The calculations are carried out using the SAGE (Solgasmix Advanced Gibbs Energy) software, by assuming ideal solid solutions between UC and PuC, as well as between U 2 C 3 and Pu 2 C 3 . The validity of the model is previously tested using published equilibrium vapour pressure data. This work gives rise to a large description of the variations of Pu losses from mixed uranium plutonium carbides and leads to some basic recommendations in connection with the use of this advanced fuel materials

Civil plutonium management

International Nuclear Information System (INIS)

Sicard, B.; Zaetta, A.

2004-01-01

During 1960 and 1970 the researches on the plutonium recycling in fast neutrons reactors were stimulated by the fear of uranium reserves diminishing. At the beginning of 1980, the plutonium mono-recycling for water cooled reactors is implementing. After 1990 the public opinion concerning the radioactive wastes management and the consequences of the disarmament agreements between Russia and United States, modified the context. This paper presents the today situation and technology associated to the different options and strategical solutions of the plutonium management: the plutonium use in the world, the neutronic characteristics, the plutonium effect on the reactors characteristics, the MOX behavior in the reactors, the MOX fabrication and treatment, the possible improvements to the plutonium use, the concepts performance in a nuclear park. (A.L.B.)

Plutonium and minor actinides recycle in equilibrium fuel cycles of pressurized water reactor

Energy Technology Data Exchange (ETDEWEB)

Waris, A.; Sekimoto, H. [Research Lab. for Nuclear Reactors, Tokyo Institute of Technology, Tokyo (Japan)

2001-07-01

A study on plutonium and minor actinides (MA) recycle in equilibrium fuel cycles of pressurized water reactors (PWR) has been performed. The calculation results showed that the enrichment and the required amount of natural uranium decrease significantly with increasing number of confined plutonium and MA when uranium is discharged from the reactor. However, when uranium is totally confined, the enrichment becomes extremely high. The recycle of plutonium and MA together with discharging uranium can reduce the radio-toxicity of discharged heavy metal (HM) waste to become less than that of loaded uranium. (author)

Testing plutonium fuel assembly production for fast-neutron reactors

International Nuclear Information System (INIS)

Nougues, B.; Benhamou, A.; Bertothy, G.; Lepetit, H.

1975-01-01

The main characteristics of plutonium fuel elements for fast breeder reactors justify specific test procedures and special techniques. The specific tests relating to the Pu content consist of Pu enrichment and distribution tests, determination of the O/M ratio and external contamination tests. The specific tests performed on fuel configuration are: testing of sintered pellet diameter, testing of pin welding and checking of internal assmbly [fr

The problem of utilization of the military uranium and plutonium

International Nuclear Information System (INIS)

Feoktistov, L.P.

1995-01-01

The problem on military uranium and plutonium is considered from the viewpoint of their utilization as a source of fissionable materials for NPPs. The solution consists in combining spherical geometry of critical mass with enriched center and the uranium burnup expansion recess. It is necessary thereby to obtain the minimum plutonium consumption in order to draw in unlimited quaintness of uranium-238 in the burnup process. It is estimated that hundred reactors with the total capacity of several hundred gigawatt may be involved into operation with the help of military plutonium. Refs. 2

Prospects for the establishment of plutonium recycle in thermal reactors in the Foratom countries. Status and assessment

International Nuclear Information System (INIS)

Chamberlain, A.; Melches, C.

1977-01-01

the fast breeder reactor, the cost and availability of uranium ore and the desirability of recycling plutonium from security considerations. (author)

A method for determining an effective porosity correction factor for thermal conductivity in fast reactor uranium-plutonium oxide fuel pellets

International Nuclear Information System (INIS)

Inoue, Masaki; Abe, Kazuyuki; Sato, Isamu

2000-01-01

A reliable method has been developed for determining an effective porosity correction factor for calculating a realistic thermal conductivity for fast reactor uranium-plutonium (mixed) oxide fuel pellets. By using image analysis of the ceramographs of transverse sections of mixed-oxide fuel pellets, the fuel morphology could be classified into two basic types. One is a 'two-phase' type that consists of small pores dispersed in the fuel matrix. The other is a 'three-phase' type that has large pores in addition to the small pores dispersed in the fuel matrix. The pore sizes are divided into two categories, large and small, at the 30 μm area equivalent diameter. These classifications lead to an equation for calculating an effective porosity correction factor by accounting for the small and large pore volume fractions and coefficients. This new analytical method for determining the effective porosity correction factor for calculating the realistic thermal conductivity of mixed-oxide fuel was also experimentally confirmed for high-, medium- and low-density fuel pellets

Using the Integral Fast Reactor (IFR) to dispose of excess weapons plutonium

International Nuclear Information System (INIS)

Hannum, W.H.; Wade, D.C.

1997-01-01

Plutonium is a man-made radioactive element with a long half-life. The only way to dispose of plutonium permanently is by causing it to fission. The fission process is efficient only in a fast neutron spectrum, and multiple recycle with a minimal loss is required to approach complete destruction. To be consistent with nonproliferation objectives, the process should be compatible with rigorous safeguards, and should not involve handling separated plutonium; The Integral Fast Reactor (IFR) meets all of these requirements. In addition, several near-term denaturing options are available that are fully compatible with complete destruction. When coupled with electrical generation, ample revenues would be available to cover all handling, operating and safeguards costs, with a substantial residual net return on the investment. (author)

Physics of Plutonium Recycling in Thermal Reactors

International Nuclear Information System (INIS)

Kinchin, G.H.

1967-01-01

A substantial programme of experimental reactor physics work with plutonium fuels has been carried out in the UK; the purpose of this paper is to review the experimental and theoretical work, with emphasis on plutonium recycling in thermal reactors. Although the main incentive for some of the work may have been to study plutonium build-up in uranium-fuelled reactors, it is nevertheless relevant to plutonium recycling and no distinction is drawn between build-up and enrichment studies. A variety of techniques have been for determining reactivity, neutron spectrum and reaction rates in simple assemblies of plutonium-aluminium fuel with water, graphite and beryllia moderators. These experiments give confidence in the basic data and methods of calculation for near-homogeneous mixtures of plutonium and moderator. In the practical case of plutonium recycling it is necessary to confirm that satisfactory predictions can be made for heterogeneous lattices enriched with plutonium. In this field, experiments have been carried out with plutonium-uranium metal and oxide-cluster fuels in graphite-moderated lattices and in SGHW lattices, and the effects of 240 Pu have been studied by perturbation measurements with single fuel elements. The exponential and critical experiments have used tonne quantities of fuel with plutonium contents ranging from 0.25 to 1.2% and the perturbation experiments have extended both the range of plutonium contents and the range of isotopic compositions of plutonium. In addition to reactivity and reactivity coefficients, such as the temperature coefficients, attention has been concentrated on relative reaction rate distributions which provide evidence for variations of neutron spectrum. .Theoretical comparisons, together with similar comparisons for non-uniform lattices, establish the validity of methods of calculation which have been used to study the feasibility of plutonium recycling in thermal reactors. (author)

Physics of Plutonium Recycling in Thermal Reactors

Energy Technology Data Exchange (ETDEWEB)

Kinchin, G. H. [Atomic Energy Establishment, Winfrith, Dorchester, Dorset (United Kingdom)

1967-09-15

A substantial programme of experimental reactor physics work with plutonium fuels has been carried out in the UK; the purpose of this paper is to review the experimental and theoretical work, with emphasis on plutonium recycling in thermal reactors. Although the main incentive for some of the work may have been to study plutonium build-up in uranium-fuelled reactors, it is nevertheless relevant to plutonium recycling and no distinction is drawn between build-up and enrichment studies. A variety of techniques have been for determining reactivity, neutron spectrum and reaction rates in simple assemblies of plutonium-aluminium fuel with water, graphite and beryllia moderators. These experiments give confidence in the basic data and methods of calculation for near-homogeneous mixtures of plutonium and moderator. In the practical case of plutonium recycling it is necessary to confirm that satisfactory predictions can be made for heterogeneous lattices enriched with plutonium. In this field, experiments have been carried out with plutonium-uranium metal and oxide-cluster fuels in graphite-moderated lattices and in SGHW lattices, and the effects of {sup 240}Pu have been studied by perturbation measurements with single fuel elements. The exponential and critical experiments have used tonne quantities of fuel with plutonium contents ranging from 0.25 to 1.2% and the perturbation experiments have extended both the range of plutonium contents and the range of isotopic compositions of plutonium. In addition to reactivity and reactivity coefficients, such as the temperature coefficients, attention has been concentrated on relative reaction rate distributions which provide evidence for variations of neutron spectrum. .Theoretical comparisons, together with similar comparisons for non-uniform lattices, establish the validity of methods of calculation which have been used to study the feasibility of plutonium recycling in thermal reactors. (author)

Review of fast reactor activities in India

Energy Technology Data Exchange (ETDEWEB)

Paranjpe, S R [Reactor Research Centre, Kalpakkam, Tamil Nadu (India)

1981-05-01

It may be recalled that In the presentation at the last meeting of the IWGFR (13th Annual meeting), a broad outline of India's nuclear energy programme and the role of fast breeders in the programme has been provided. The steps taken to enable the fast breeders to fulfil their role have also been described. In brief, fast breeder reactors are considered as an essential and integral part of the programme of nuclear energy and constitute the second step in the programme, the first being the construction of natural uranium heavy water moderated reactors which will consume natural uranium but will produce plutonium to fuel fast breeder reactors. This basic position has remained unchanged and the Government is now taking steps to build a large number of heavy water reactors, say 10 million Kw capacity in the next 20 years. This defines the time frame for developing the fast breeder technology in the country. It has therefore been decided to mobilise the efforts towards design, construction and operation of a medium sized (about 500 M We) reactor by mid-nineties. Thus, the climate for fast breeder reactors is good and there is a good deal of enthusiasm amongst the scientists and engineers working in the field although the actual implementation of the programme during the year had to face certain difficulties.

Review of fast reactor activities in India

International Nuclear Information System (INIS)

Paranjpe, S.R.

1981-01-01

It may be recalled that In the presentation at the last meeting of the IWGFR (13th Annual meeting), a broad outline of India's nuclear energy programme and the role of fast breeders in the programme has been provided. The steps taken to enable the fast breeders to fulfil their role have also been described. In brief, fast breeder reactors are considered as an essential and integral part of the programme of nuclear energy and constitute the second step in the programme, the first being the construction of natural uranium heavy water moderated reactors which will consume natural uranium but will produce plutonium to fuel fast breeder reactors. This basic position has remained unchanged and the Government is now taking steps to build a large number of heavy water reactors, say 10 million Kw capacity in the next 20 years. This defines the time frame for developing the fast breeder technology in the country. It has therefore been decided to mobilise the efforts towards design, construction and operation of a medium sized (about 500 M We) reactor by mid-nineties. Thus, the climate for fast breeder reactors is good and there is a good deal of enthusiasm amongst the scientists and engineers working in the field although the actual implementation of the programme during the year had to face certain difficulties

Simulating the Behaviour of the Fast Reactor Joyo (Draft)

International Nuclear Information System (INIS)

Juutilainen, Pauli

2008-01-01

Motivated by the development of fast reactors the behaviour of the Japanese experimental fast reactor Joyo is simulated with two Monte Carlo codes: Monte Carlo NParticle (MCNP) and Probabilistic Scattering Game (PSG). The simulations are based on the benchmark study 'Japan's Experimental Fast Reactor Joyo MKI core: Sodium-Cooled Uranium-Plutonium Mixed Oxide Fueled Fast Core Surrounded by UO 2 Blanket'. The study is focused on the criticality of the reactor, control rod worth, sodium void reactivity and isothermal temperature coefficient of the reactor. These features are calculated by applying both homogeneous and heterogeneous reactor core models that are built according to the benchmark instructions. The results of the two models obtained by the two codes are compared with each other and especially with the experimental results presented in the benchmark. (author)

Pyrometallurgical processing of Integral Fast Reactor metal fuels

International Nuclear Information System (INIS)

Battles, J.E.; Miller, W.E.; Gay, E.C.

1991-01-01

The pyrometallurgical process for recycling spent metal fuels from the Integral Fast Reactor is now in an advanced state of development. This process involves electrorefining spent fuel with a cadmium anode, solid and liquid cathodes, and a molten salt electrolyte (LiCl-KCl) at 500 degrees C. The initial process feasibility and flowsheet verification studies have been conducted in a laboratory-scale electrorefiner. Based on these studies, a dual cathode approach has been adopted, where uranium is recovered on a solid cathode mandrel and uranium-plutonium is recovered in a liquid cadmium cathode. Consolidation and purification (salt and cadmium removal) of uranium and uranium-plutonium products from the electrorefiner have been successful. The process is being developed with the aid of an engineering-scale electrorefiner, which has been successfully operated for more than three years. In this electrorefiner, uranium has been electrotransported from the cadmium anode to a solid cathode in 10 kg quantities. Also, anodic dissolution of 10 kg batches of chopped, simulated fuel (U--10% Zr) has been demonstrated. Development of the liquid cadmium cathode for recovering uranium-plutonium is under way

Enriched uranium cycles in pressurized heavy water reactors

International Nuclear Information System (INIS)

Mazzola, A.

1994-01-01

A study was made on the substitution of natural uranium with enriched and on plutonium recycle in unmodified PHWRs (pressure vessel reactor). Results clearly show the usefulness of enriched fuel utilisation for both uranium ore consumption (savings of 30% around 1.3% enrichment) and decreasing fuel cycle coasts. This is also due to a better plutonium exploitation during the cycle. On the other hand plutonium recycle in these reactors via MOX-type fuel appears economically unfavourable under any condition

Grain growth kinetics in uranium-plutonium mixed oxides

International Nuclear Information System (INIS)

Sari, C.

1986-01-01

Grain growth rates were investigated in uranium-plutonium mixed oxide specimens with oxygen-to-metal ratios 1.97 and 2.0. The specimens in the form of cylindrical pellets were heated in a temperature gradient similar to that existing in a fast reactor. The results are in agreement with the cubic rate law. The mean grain size D(μm) after annealing for time t (min) is represented by D 3 -D 0 3 =1.11x10 12 . exp(-445870/RT).t and D 3 -D 0 3 =2.55x10 9 .exp(-319240/RT).t for specimens with overall oxygen-to-metal ratios 1.97 and 2.0, respectively (activation energies expressed in J/mol). An example for the influence of the oxygen-to-metal ratio on the grain growth in mixed oxide fuel during operation in a fast reactor is also given. (orig.)

Uranium and thorium cycles for sodium fast reactors: Neutronic aspects and associated wastes

International Nuclear Information System (INIS)

Brizi, J.

2010-10-01

Sodium fast reactors (SFR-Na) with uranium 238/plutonium 239(U/Pu) cycle, its technical feasibility has already proven, allow to overcome the problem of natural uranium resources in achieving the regeneration of the fuel fissile element. In addition, a waste management can be performed to reduce the radiotoxicity of actinides produced by the reactor in transmuting the AM in the core (homogeneous transmutation). Another alternative to minimize waste is to use another couple fertile-fissile: the thorium 232 and the uranium 233 (Th/U). The comparison is performed on neutronic and safety aspects and on waste production, in using an evolutive Monte Carlo. Although one does not disclose real clear advantages concerning the radiotoxicity of wastes for a particular cycle, the Th/U cycle reduces the radiotoxicity during periods when it is the highest. The homogeneous transmutation minimizes significantly for both cycles, radiotoxicity of wastes, with different factors depending on the considered time period. However, it is done to the detriment of an important increase of AM in the core. If we consider the nuclear stop, the inventory of the reactor core becomes a waste. The gain provided by the transmutation, taking into account both the core and accumulated waste radio-toxicities, will be quantified, and shows the transmutation does not provide a significant gain if the burning of main fissile elements is not considered when the nuclear is stopped. (author)

Build-up and decay of fuel actinides in the fuel cycle of nuclear reactors

International Nuclear Information System (INIS)

Tasaka, Kanji; Kikuchi, Yasuyuki; Shindo, Ryuichi; Yoshida, Hiroyuki; Yasukawa, Shigeru

1976-05-01

For boiling water reactors, pressurized light-water reactors, pressure-tube-type heavy water reactors, high-temperature gas-cooled reactors, and sodium-cooled fast breeder reactors, uranium fueled and mixed-oxide fueled, each of 1000 MWe, the following have been studied: (1) quantities of plutonium and other fuel actinides built up in the reactor, (2) cooling behaviors of activities of plutonium and other fuel actinides in the spent fuels, and (3) activities of plutonium and other fuel actinides in the high-level reprocessing wastes as a function of storage time. The neutron cross section and decay data of respective actinide nuclides are presented, with their evaluations. For effective utilization of the uranium resources and easy reprocessing and high-level waste management, a thermal reactor must be fueled with uranium; the plutonium produced in a thermal reactor should be used in a fast reactor; and the plutonium produced in the blanket of a fast reactor is more appropriate for a fast reactor than that from a thermal reactor. (auth.)

Plutonium Consumption Program, CANDU Reactor Project final report

Energy Technology Data Exchange (ETDEWEB)

1994-07-31

DOE is investigating methods for long term dispositioning of weapons grade plutonium. One such method would be to utilize the plutonium in Mixed OXide (MOX) fuel assemblies in existing CANDU reactors. CANDU (Canadian Deuterium Uranium) reactors are designed, licensed, built, and supported by Atomic Energy of Canada Limited (AECL), and currently use natural uranium oxide as fuel. The MOX spent fuel assemblies removed from the reactor would be similar to the spent fuel currently produced using natural uranium fuel, thus rendering the plutonium as unattractive as that in the stockpiles of commercial spent fuel. This report presents the results of a study sponsored by the DOE for dispositioning the plutonium using CANDU technology. Ontario Hydro`s Bruce A was used as reference. The fuel design study defined the optimum parameters to disposition 50 tons of Pu in 25 years (or 100 tons). Two alternate fuel designs were studied. Safeguards, security, environment, safety, health, economics, etc. were considered. Options for complete destruction of the Pu were also studied briefly; CANDU has a superior ability for this. Alternative deployment options were explored and the potential impact on Pu dispositioning in the former Soviet Union was studied. An integrated system can be ready to begin Pu consumption in 4 years, with no changes required to the reactors other than for safe, secure storage of new fuel.

Plutonium Consumption Program, CANDU Reactor Project final report

International Nuclear Information System (INIS)

1994-01-01

DOE is investigating methods for long term dispositioning of weapons grade plutonium. One such method would be to utilize the plutonium in Mixed OXide (MOX) fuel assemblies in existing CANDU reactors. CANDU (Canadian Deuterium Uranium) reactors are designed, licensed, built, and supported by Atomic Energy of Canada Limited (AECL), and currently use natural uranium oxide as fuel. The MOX spent fuel assemblies removed from the reactor would be similar to the spent fuel currently produced using natural uranium fuel, thus rendering the plutonium as unattractive as that in the stockpiles of commercial spent fuel. This report presents the results of a study sponsored by the DOE for dispositioning the plutonium using CANDU technology. Ontario Hydro's Bruce A was used as reference. The fuel design study defined the optimum parameters to disposition 50 tons of Pu in 25 years (or 100 tons). Two alternate fuel designs were studied. Safeguards, security, environment, safety, health, economics, etc. were considered. Options for complete destruction of the Pu were also studied briefly; CANDU has a superior ability for this. Alternative deployment options were explored and the potential impact on Pu dispositioning in the former Soviet Union was studied. An integrated system can be ready to begin Pu consumption in 4 years, with no changes required to the reactors other than for safe, secure storage of new fuel

PRISM reactor. An option for plutonium disposition?

Energy Technology Data Exchange (ETDEWEB)

Fehlinger, Sebastian; Friess, Friederike; Kuett, Moritz [IANUS, Technische Universitaet Darmstadt (Germany)

2015-07-01

The Power Reactor Innovative Small Module (PRISM) is sodium cooled fast reactor model. The energy output depends on the core configuration, however with an energy output of approximately 300 MWe, the PRISM reactor belongs to the class of small modular reactors. Beside using the reactor as a breeder reactor or for the transmutation of nuclear waste, it might also be used as a burner reactor for separated plutonium. This includes for example U.S.-American excess weapon-grade plutonium as well as separated reactor-grade plutonium. Recently, there has been an ongoing discussion in GB to use the PRISM reactor to dispose their excess civilian plutonium. Depending on the task, the core configuration varies slightly. We will present different layouts and the matching MCNP models, these models can then be used to conduct depletion calculations. From these results, analysis of the change in the plutonium isotopics in the spent fuel, the amount of fissioned plutonium, and the possible annual plutonium throughputs is possible.

Proserpine - plutonium 239 - Proserpine - uranium 235 - comparison of experimental results; Proserpine - plutonium 239 - proserpine - uranium 235 - comparaison de resultats experimentaux

Energy Technology Data Exchange (ETDEWEB)

Brunet, J P; Caizergues, R; Clouet D' Orval, Ch; Kremser, J; Moret-Bailly, J; Verriere, Ph [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1964-07-01

The Proserpine homogeneous reactor is constituted by a tank, 25 cm dia, 30 cm high, surrounded by a composite reflector made of beryllium oxide and graphite. In this tank can be made critical plutonium or 90 per cent enriched uranium solutions, the fissile substances being in the form of a dissolved salt. In varying the concentration of the solution, critical masses were studied as a function of the level of the liquid in the tank. The minimum critical mass is 256 {+-} 2 grs for plutonium and 409 {+-} 3 grs for uranium 235. In the range of the critical concentrations which were studied, the neutronic properties of fissionable solutions of plutonium and enriched uranium were compared for identical geometries. (authors) [French] Proserpine est un reacteur homogene comportant une cuve de diametre 25 cm, de hauteur 30 cm, entouree d'un reflecteur composite d'oxyde de beryllium et de graphite. On y a rendu critiques des solutions de plutonium ou d'uranium enrichi a 90 pour cent, le produit fissile se trouvant sous la forme d'un sel dissous. En faisant varier la concentration de la solution, on a etudie les masses critiques en fonction de la hauteur du liquide dans la cuve. La masse- critique minimum est, pour le plutonium de 256 {+-} 2 g, pour l'uranium 235 de 409 {+-} 3 g. Dans la gamme des concentrations critiques etudiees, on a compare, dans des conditions de geometrie identique, les proprietes neutroniques des solutions fissiles de plutonium et d'uranium enrichi. (auteurs)

The integral fast reactor fuel cycle

International Nuclear Information System (INIS)

Chang, Y.I.

1990-01-01

The liquid-metal reactor (LMR) has the potential to extend the uranium resource by a factor of 50 to 100 over current commercial light water reactors (LWRs). In the integral fast reactor (IFR) development program, the entire reactor system - reactor, fuel cycle, and waste process - is being developed and optimized at the same time as a single integral entity. A key feature of the IFR concept is the metallic fuel. The lead irradiation tests on the new U-Pu-Zr metallic fuel in the Experimental Breeder Reactor II have surpassed 185000 MWd/t burnup, and its high burnup capability has now been fully demonstrated. The metallic fuel also allows a radically improved fuel cycle technology. Pyroprocessing, which utilizes high temperatures and molten salt and molten metal solvents, can be advantageously utilized for processing metal fuels because the product is metal suitable for fabrication into new fuel elements. Direct production of a metal product avoids expensive and cumbersome chemical conversion steps that would result from use of the conventional Purex solvent extraction process. The key step in the IFR process is electrorefining, which provides for recovery of the valuable fuel constituents, uranium and plutonium, and for removal of fission products. A notable feature of the IFR process is that the actinide elements accompany plutonium through the process. This results in a major advantage in the high-level waste management

Plutonium-enriched thermal fuel production experience in Belgium

International Nuclear Information System (INIS)

LeBlanc, J.M.

1983-01-01

Taking into account the strategic aspects of nuclear energy such as availability and sufficiency of resources and independence of energy supply, most countries planning to use plutonium look mainly to its use in fast reactors. However, by recycling the recovered uranium and plutonium in light water reactors, the saving of the uranium that would otherwise be required could already be higher than 35%. Therefore, until fast reactors are introduced, for macro- or microeconomic reasons, the plutonium recycle option seems to be quite valuable for countries having the plutonium technology. In Belgium, Belgonucleaire has been developing the plutonium technology for more than 20 yr and has operated a mixed oxide fuel fabrication plant since 1973. The past ten years of plant operation have provided for many improvements and relevant new documented experiences establishing a basis for new modifications that will be beneficial to the intrinsic quality, overall safety, and economy of the fuel

Plutonium assemblies in reload 1 of the Dodewaard Reactor

International Nuclear Information System (INIS)

Bairiot, H.; Deramaix, P.; Vandenberg, C.; Leenders, L.; Mostert, P.

1977-01-01

Since 1963, Belgonucleaire has been developing the design of plutonium assemblies of the island type (i.e., plutonium rods inserted in the control zone of the assembly and enriched uranium rods at the periphery) for light water reactors. The application to boiling water reactors (BWRs) led to the introduction, in April 1971, of two prototype plutonium island assemblies in the Dodewaard BWR (The Netherlands): Those assemblies incorporating plutonium in 42 percent of the rods are interchangeable with standard uranium assemblies of the same reload. Their design, which had to meet these criteria, was performed using the routine order in use at Belgonucleaire; experimental checks included a mock-up configuration simulated in the VENUS critical facility at Mol and open-vessel cold critical experiments performed in the Dodewaard core. The pelleted plutonium rods were fabricated and controlled by Belgonucleaire following the manufacturing procedures developed at the production plant. In one of the assemblies, three vibrated plutonium fuel rods with a lower fuel density were introduced in the three most highly rated positions to reduce the power rating. Those plutonium assemblies experienced peak pellet ratings up to 535 W/cm and were discharged in April 1974 after having reached a mean burnup of approximately 21,000 MWd/MT. In-core instrumentation during operation, visual examinations, and reactivity substitution experiments during reactor shutdown did not indicate any special feature for those assemblies compared to the standard uranium assemblies, thereby demonstrating their interchangeability

Plutonium fuel an assessment. Report by an expert group

International Nuclear Information System (INIS)

Anon.

1989-01-01

Since the 1950s, plutonium used in fast reactors has been seen as the key to unlocking the vast energy resources contained in the world's uranium reserves. However, the slowing down in projected installation rates of nuclear reactors, combined with discovery of additional uranium, have led to a postponement of the point in time when fast reactors will make large demands on plutonium supplies. There are several options concerning its use or storage in the meantime. This report sets out the facts and current views about plutonium and its civil use, both at present and in the medium term. It explains the factors influencing the choice of fuel options and illustrates how economic and logistic assessments of the alternatives can be undertaken

Design characteristics of research zero power fast reactor Lasta

International Nuclear Information System (INIS)

Milosevic, M.; Stefanovic, D.; Pesic, M.; Nikolic, D.; Antic, D.; Zavaljevski, N.; Popovic, D.

1990-01-01

LASTA is a flexible zero power reactor with uranium and plutonium fuel designed for research in the neutron physics and in the fast reactor physics. Safety considerations and experimental flexibility led to the choice of a fixed vertical assembly with two safety blocks as the main safety elements, so that safety devices would be operated by gravity. The neutron and reactor physics, the control and safety philosophy adopted in our design, are described in this paper. Developed computer programs are presented. (author)

Plutonium production and utilization forecasts in Europe

International Nuclear Information System (INIS)

Haijtink, B.

1976-01-01

The planned accelerated growth of nuclear energy generation in the near future will lead to a large production of plutonium in the thermal reactors. Therefore, up to 1985, the major part of the available plutonium will be plutonium recovered from spent uranium-metal, particularly in the United Kingdom and in France. Because of the low demand for fuelling the fast breeder reactors within the near future, a surplus of fissile plutonium will be accumulated in Europe. Even if the planned availability of the oxide reprocessing capacity will be delayed with two or three years, a plutonium surplus will still exist in Europe, e.g.; in 1985: 25-20 tons. On longer term, up to 2000, the plutonium production in thermal reactors will be sufficient to meet the estimated demand for fast breeder reactors at their commercial introduction foreseen for the nineties. That means that all the plutonium surplus needs not to be stocked for use in fast breeder reactors later on but could be recycled in thermal reactors. The magnitude of the available fissionable materials give an idea of the importance to promote, on an industrial scale, the plutonium recycling technology

Benchmark tests of JENDL-3.2 for thermal and fast reactors

International Nuclear Information System (INIS)

Takano, Hideki

1995-01-01

Benchmark calculations for a variety of thermal and fast reactors have been performed by using the newly evaluated JENDL-3 Version-2 (JENDL-3.2) file. In the thermal reactor calculations for the uranium and plutonium fueled cores of TRX and TCA, the k eff and lattice parameters were well predicted. The fast reactor calculations for ZPPR-9 and FCA assemblies showed that the k eff , reactivity worth of Doppler, sodium void and control rod, and reaction rate distribution were in a very good agreement with the experiments. (author)

Uranium alloys for using in fast breeder reactors

International Nuclear Information System (INIS)

Moura Neto, C.; Pires, O.S.

1988-08-01

The U-Zr and U-Ti alloys are studied, given emphasis to the high solute solubility in gamma phase of uranium, which is suitable for using as metal fuel in fast breeder reactors. The alloys were prepared in electron beam furnaces and submitted to X-ray diffraction, X-ray fluorescence, microhardness, optical metallography, and chemical analysis. The obtained values are good agreements with the literature data. The study shows that the U-Zr presents better characteristics than the U-Ti for using as fuel in fast breeder reactors. (M.C.K.) [pt

Quantities of actinides in nuclear reactor fuel cycles

International Nuclear Information System (INIS)

Ang, K.P.

1975-01-01

The quantities of plutonium and other fuel actinides have been calculated for equilibrium fuel cycles for 1000 MW reactors of the following types: water reactors fueled with slightly enriched uranium, water reactors fueled with plutonium and natural uranium, fast-breeder reactors, gas-cooled reactors fueled with thorium and highly enriched uranium, and gas-cooled reactors fueled with thorium, plutonium, and recycled uranium. The radioactivity levels of plutonium, americium, and curium processed yearly in these fuel cycles are greatest for the water reactors fueled with natural uranium and recycled plutonium. The total amount of actinides processed is calculated for the predicted future growth of the United States nuclear power industry. For the same total installed nuclear power capacity, the introduction of the plutonium breeder has little effect upon the total amount of plutonium processed in this century. The estimated amount of plutonium in the low-level process wastes in the plutonium fuel cycles is comparable to the amount of plutonium in the high-level fission product wastes. The amount of plutonium processed in the nuclear fuel cycles can be considerably reduced by using gas-cooled reactors to consume plutonium produced in uranium-fueled water reactors. These, and other reactors dedicated for plutonium utilization, could be co-located with facilities for fuel reprocessing and fuel fabrication to eliminate the off-site transport of separated plutonium. (U.S.)

Method to manufacture a nuclear fuel from uranium-plutonium monocarbide or uranium-plutonium mononitride

International Nuclear Information System (INIS)

Krauth, A.; Mueller, N.

1977-01-01

Pure uranium carbide or nitride is converted with plutonium oxide and carbon (all in powder form) to uranium-plutonium monocarbide or mononitride by cold pressing and sintering at about 1600 0 C. Pure uranium carbide or uranium nitride powder is firstly prepared without extensive safety measures. The pure uranium carbide or nitride powder can also be inactivated by using chemical substances (e.g. stearic acid) and be handled in air. The sinterable uranium carbide or nitride powder (or also granulate) is then introduced into the plutonium line and mixed with a nonstoichiometrically adjusted, prereacted mixture of plutonium oxide and carbon, pressed to pellets and reaction sintered. The surface of the uranium-plutonium carbide (higher metal content) can be nitrated towards the end of the sinter process in a stream of nitrogen. The protective layer stabilizes the carbide against the water and oxygen content in air. (IHOE) [de

The use of plutonium in Swedish reactors

International Nuclear Information System (INIS)

Forsstroem, H.

1982-09-01

The report deals with the utilization of plutonium in Swedish nuclear power plants. The plutonium content of the mixed oxide fuel will normally be 3-7 per cent. The processing of spent nuclear fuel will produce about 6 ton plutonium. The use of mixed oxide fuel in Forsmark 3 and Oskarshamn 3 is discussed. The fuel cycle will start with the manufacturing of the fuel elements abroad and proceeds with transport and utilization, storing of spent fuel about 40 years in Sweden followed by direct disposal. The manufacture and use of mixed oxide (MOX) fuel is based on well-known techniques. Approximately 20 000 MOX fuel rods have been irradiated and the fuel is essentially equivalent to uranium oxide fuel. 30-50 per cent of the core may be composed of MOX-fuel without any effect on the operation and safety of the reactor which has been originally designed for uranium fuel. The evaluation of international fuel cycle (INFCE) states that the proliferation risks are very small. The recycling of plutonium will reduce demand for enriched uranium and the calculations show that 6.3 ton plutonium will replace the enrichment of 600 ton natural uranium. (G.B.)

Economic analysis of self-generated plutonium recycling in light water reactor

International Nuclear Information System (INIS)

Deguchi, Morimoto; Hirabayashi, Fumio; Yumoto, Ryozo

1978-01-01

This paper describes on the economics of plutonium recycle to light water reactors (LWRs). In the situation that plutonium market does not exist, it is realistic for utilities to recycle the self-generated plutonium to their own reactors. The economic incentive to recycle self-generated plutonium, plutonium fuel fabrication penalty, and the dependence of fuel cycle cost on fuel cycle cost parameters are considered. In recycling self-generated plutonium, two alternatives for fuel element design are feasible. Those are the all-plutonium design and the island design. In the present analysis, the all-plutonium design was chosen for PWRs. The calculation of reactivity variation along with burnup for both uranium fuel and plutonium fuel was done with LASER-PNC code. Plutonium inventory and other nuclear data were calculated with CHAIN code. It is expected that equilibrium composition is reached after 5 or 6 times of recycling. For the calculation of fuel cycle cost, MITCOST code was used. The recent increase in the prices of uranium ore, enrichment and reprocessing services was taken into account. The fuel cycle cost of plutonium recycle is lower than that of uranium fuel cycle within a certain limit of plutonium fabrication penalty. It is shown that the fabrication penalty of about 1250 dollar/kgHM for each plutonium successive recycle reduces the cost difference to zero. The change in other cost components affects break-even fabrication penalty, in which the fuel cycle cost of plutonium recycle is equal to that of uranium cycle. (Kato, T.)

Study of reactions between uranium-plutonium mixed oxide and uranium nitride and between uranium oxide and uranium nitride; Etude des reactions entre l`oxyde mixte d`uranium-plutonium et le nitrure d`uranium et entre l`oxyde d`uranium et le nitrure d`uranium

Energy Technology Data Exchange (ETDEWEB)

Lecraz, C

1993-06-11

A new type of combustible elements which is a mixture of uranium nitride and uranium-plutonium oxide could be used for Quick Neutrons Reactors. Three different studies have been made on the one hand on the reactions between uranium nitride (UN) and uranium-plutonium mixed oxide (U,Pu)O{sub 2}, on the other hand on these between UN and uranium oxide UO{sub 2}. They show a sizeable reaction between nitride and oxide for the studied temperatures range (1573 K to 1973 K). This reaction forms a oxynitride compound, MO{sub x} N{sub y} with M=U or M=(U,Pu), whose crystalline structure is similar to oxide`s. Solubility of nitride in both oxides is studied, as the reaction kinetics. (TEC). 32 refs., 48 figs., 22 tabs.

Radionuclide compositions of spent fuel and high level waste for the uranium and plutonium fuelled PWR

International Nuclear Information System (INIS)

Fairclough, M.P.; Tymons, B.J.

1985-06-01

The activities of a selection of radionuclides are presented for three types of reactor fuel of interest in radioactive waste management. The fuel types are for a uranium 'burning' PWR, a plutonium 'burning' PWR using plutonium recycled from spent uranium fuel and a plutonium 'burning' PWR using plutonium which has undergone multiple recycle. (author)

Studies on O/M ratio determination in uranium oxide, plutonium oxide and uranium-plutonium mixed oxide

International Nuclear Information System (INIS)

Sampath, S.; Chawla, K.L.

1975-01-01

Thermogravimetric studies were carried out in unsintered and sintered samples of uranium oxide, plutonium oxide and uranium-plutonium mixed oxide under different atmospheric conditions (air, argon and moist argon/hydrogen). Moisture loss was found to occur below 200 0 C for uranium dioxide samples, upto 700 0 C for sintered plutonium dioxide and negligible for sintered samples. The O/M ratios for non-stoichiometric uranium dioxide (sintered and unsintered), plutonium dioxide and mixed uranium and plutonium oxides (sintered) could be obtained with a precision of +- 0.002. Two reference states UOsub(2.000) and UOsub(2.656) were obtained for uranium dioxide and the reference state MOsub(2.000) was used for other cases. For unsintered plutonium dioxide samples, accurate O/M ratios could not be obtained of overlap of moisture loss with oxygen loss/gain. (author)

Proserpine - plutonium 239 - Proserpine - uranium 235 - comparison of experimental results

International Nuclear Information System (INIS)

Brunet, J.P.; Caizergues, R.; Clouet D'Orval, Ch.; Kremser, J.; Moret-Bailly, J.; Verriere, Ph.

1964-01-01

The Proserpine homogeneous reactor is constituted by a tank, 25 cm dia, 30 cm high, surrounded by a composite reflector made of beryllium oxide and graphite. In this tank can be made critical plutonium or 90 per cent enriched uranium solutions, the fissile substances being in the form of a dissolved salt. In varying the concentration of the solution, critical masses were studied as a function of the level of the liquid in the tank. The minimum critical mass is 256 ± 2 grs for plutonium and 409 ± 3 grs for uranium 235. In the range of the critical concentrations which were studied, the neutronic properties of fissionable solutions of plutonium and enriched uranium were compared for identical geometries. (authors) [fr

Electrochemistry in fast reactor technology

International Nuclear Information System (INIS)

Mathews, C.K.

1987-01-01

Electrochemistry plays a significant role in the production, characterisation or behaviour of the fuel, the coolant and structural materials used in fast reactor systems. The role of electrochemistry in sodium production, in the fuel cycle, in the development of electrochemical meters used for the on-line monitoring of the various impurities at sub ppm levels and in the recovery of plutonium and uranium are discussed. The advantage of voltammmetric techniques in the analysis of impurities and the application of electrochemical meters have been investigated. (author). 5 figs., 15 refs

On the Burning of Plutonium Originating from Light Water Reactor Use in a Fast Molten Salt Reactor—A Neutron Physical Study

Directory of Open Access Journals (Sweden)

Bruno Merk

2015-11-01

Full Text Available An efficient burning of the plutonium produced during light water reactor (LWR operation has the potential to significantly improve the sustainability indices of LWR operations. The work offers a comparison of the efficiency of Pu burning in different reactor configurations—a molten salt fast reactor, a LWR with mixed oxide (MOX fuel, and a sodium cooled fast reactor. The calculations are performed using the HELIOS 2 code. All results are evaluated against the plutonium burning efficiency determined in the Consommation Accrue de Plutonium dans les Réacteurs à Neutrons RApides (CAPRA project. The results are discussed with special view on the increased sustainability of LWR use in the case of successful avoidance of an accumulation of Pu which otherwise would have to be forwarded to a final disposal. A strategic discussion is given about the unavoidable plutonium production, the possibility to burn the plutonium to avoid a burden for the future generations which would have to be controlled.

Core characteristics on a hybrid type fast reactor system combined with proton accelerator

International Nuclear Information System (INIS)

Kowata, Yasuki; Otsubo, Akira

1997-06-01

In our study on a hybrid fast reactor system, we have investigated it from the view point of transmutation ability of trans-uranium (TRU) nuclide making the most effective use of special features (controllability, hard neutron spectrum) of the system. It is proved that a proton beam is superior in generation of neutrons compared with an electron beam. Therefore a proton accelerator using spallation reaction with a target nucleus has an advantage to transmutation of TRU than an electron one. A fast reactor is expected to primarily have a merit that the reactor can be operated for a long term without employment of highly enriched plutonium fuel by using external neutron source such as the proton accelerator. Namely, the system has a desirable characteristic of being possible to self-sustained fissile plutonium. Consequently in the present report, core characteristics of the system were roughly studied by analyses using 2D-BURN code. The possibility of self-sustained fuel was investigated from the burnup and neutronic calculation in a cylindrical core with 300w/cc of power density without considering a target material region for the accelerator. For a reference core of which the height and the radius are both 100 cm, there is a fair prospect that a long term reactor operation is possible with subsequent refueling of natural uranium, if the medium enriched (around 10wt%) uranium or plutonium fuels are fully loaded in the initial core. More precise analyses will be planed in a later fiscal year. (author)

Fast reactor operation in the United States

International Nuclear Information System (INIS)

Smith, R.R.; Cissel, D.W.

1978-01-01

Of the many American facilities dedicated to fast reactor technology, six qualify as liquid-metal-cooled fast reactors. All of these satisfy the following criteria: an unmoderated neutron spectrum, highly enriched fuel material, substantial heat production, and the use of a liquid metal coolant. These include the following: EBR-I Clementine, LAMPRE, EBR-II, EFFBR, and SEFOR. Collectively, these facilities encompassed all of the more important features of liquid-metal-cooled fast reactor technology. Coolant types ranged from mercury in Clementine, to NaK in EBR-I, and sodium in the others. Fuels included enriched-uranium metallic alloys in EBR-I, EBR-II, and EFFBR; metallic plutonium in Clementine; molten plutonium alloy in LAMPRE; and a mixed UO 2 -PuO 2 ceramic in SEFOR. Heat removal techniques ranged from air-blast cooling in LAMPRE and SEFOR; steam-electrical generation in EBR-I, EBR-II, and EFFBR; to a mercury-to-water heat dump in Clementine. Operational experience with such diverse systems has contributed heavily to the U.S. Each of the six systems is described from the viewpoints of purpose, history, design, and operation. Attempts are made to limit descriptive material to the most important features and to refer the reader to a few select references if additional information is needed

Development of a fresh plutonium fuel container for a prototype fast breeder reactor

International Nuclear Information System (INIS)

Ohtake, T.; Takahashi, S.; Mishima, T.; Kurakami, J.; Yamamoto, Y.; Ohuchi, Y.

1989-01-01

Japan gives a good deal of encouragement to development of a fast breeder reactor (which is considered as the most likely candidate for nuclear power generation) to secure long-term energy source. And, following an experimental fast breeder reactor Joyo, a prototype fast breeder reactor Monju is now under vigorous construction. Related to development of the prototype fast breeder reactor, it is necessary and important to develop transport container which is used for transporting fresh fuel assemblies from Plutonium Fuel Production Facility to the Monju power plant. Therefore, the container is now being developed by Power Reactor and Nuclear Fuel Development Corporation (PNC). Currently, shipment and vibration tests, handling performance tests, shielding performance tests and prototype container tests are executed with prototype containers fabricated according to a final design, in order to experimentally confirm soundness of transport container and its contents, and propriety of design technique. This paper describes the summary of general specifications and structures of this container and the summary of preliminary safety analysis of package

Imperatives for using plutonium in commercial power reactors

International Nuclear Information System (INIS)

Sandquist, G.M.; Kunze, J.F.

1995-01-01

The use of reprocessed or newly produced plutonium as a fissile fuel in commercial nuclear reactors in the US has been actively suppressed by the current US Administration. Yet, many other advanced nations have already adopted mixed oxide fuels which are manufactured from a mixture of plutonium and natural uranium compounds. These nations have successfully proven the use of such nuclear fuel in their commercial power reactors for many years. The full consequence of the restrictive nuclear policy in the US will greatly limit the lifetime of the nuclear fuel resources in the US from a nominal potential of 100 centuries or more of potential energy supply to about 50 years or less at economical prices for uranium. This paper addresses both the imperatives and the potential and the perceived hazards of plutonium utilization and examines the consequences of government policy regarding utilization of nuclear power

AFCI : Co-extraction impacts on LWR and fast reactor fuel cycles

International Nuclear Information System (INIS)

Taiwo, T. A.; Szakalay, F. J.; Kim, T. K.; Hill, R. N.; Nuclear Engineering Division

2007-01-01

A systematic investigation of the impact of the co-extraction COEXTM process on reactor performance has been performed. The proliferation implication of the process was also evaluated using the critical mass, radioactivity, decay heat and neutron and gamma source rates and gamma doses as indicators. The use of LWR-spent-uranium-based MOX fuel results in a higher initial plutonium content requirement in an LWR MOX core than if natural uranium based MOX fuel is used (by about 1%); the plutonium for both cases is derived from the spent LWR spent fuel. More transuranics are consequently discharged in the spent fuel of the MOX core. The presence of U-236 in the initial fuel was also found to result in higher content of Np-237 in the spent MOX fuel and less consumption of Pu-238 and Am-241 in the MOX core. The higher quantities of Np-237 (factor of 5), Pu-238 (20%) and Am-241 (14%) decrease the effective repository utilization, relative to the use of natural uranium in the PWR MOX core. Additionally, the minor actinides continue to accumulate in the fuel cycle, even if the U-Pu co-extraction products are continuously recycled in the PWR cores, and thus a solution is required for the minor actinides. The utilization of plutonium derived from LWR spent fuel versus weapons-grade plutonium for the startup core of a 1,000 MWT advanced burner fast reactor (ABR) increases the TRU content by about 4%. Differences are negligible for the equilibrium recycle core. The impact of using reactor spent uranium instead of depleted uranium was found to be relatively smaller in the fast reactor (TRU content difference less than 0.4%). The critical masses of the co-extraction products were found to be higher than that of weapons-grade plutonium and the decay heat and radiation sources of the materials (products) were also found to be generally higher than that of weapons-grade plutonium (WG-Pu) in the transuranics content range of 0.1 to 1.0 in the heavy-metal. The magnitude of the

Plutonium use - present status and perspectives

International Nuclear Information System (INIS)

Dievoet, J. van; Fossoul, E.; Jonckheere, E.; Bemden, E. van den

1977-01-01

Plutonium is being produced in increasing quantities in the so-called proven reactors, which are mostly of the light-water type. Evaluation of this production on a world scale shows that it would be theoretically possible to construct a large number of breeders and thus to make the best use of the intrinsic qualities of plutonium as a fissionable material, while considerably reducing the consumption of uranium. This source of plutonium is nevertheless dependent on an essential stage of the fuel cycle, namely reprocessing of irradiated fuel. The long delays in installing an adequate world reprocessing capacity are substantially weakening the prospects for the introduction of breeders. Furthermore, the critical situation as regards reprocessing may delay the development of complementary reprocessing methods for fuels with a high plutonium content and high burn-up. When it is recalled that fast reactors themselves may suffer some delay in their technological development, if only because of the intention to build power plants of very high unit capacity immediately, it must be concluded that another use will have to be considered for the plutonium available in future -use in thermal reactors, i.e. recycling. The recycling of plutonium is a well-known technique today and the objections which could be raised against it hardly stand up to analysis. Utilization of plutonium offers an appreciable saving in terms of uranium and separative work units, the consumption being of a low order of magnitude in comparison with the total amount of plutonium needed for the eventual fabrication of the first fast reactor cores. It can also be shown that immediate reprocessing of the recycling fuel is not essential for the economics of the concept. Temporary storage of recycled fuel has the advantage of concentrating plutonium in a particularly safe form, namely in irradiated plutonium-bearing fuel assemblies. Lastly, recycling offers such flexibility that it does not in practice represent

Integral measurement of fission products capture in fast breeder reactors

International Nuclear Information System (INIS)

Martin Deidier, Loick.

1979-12-01

For the SUPERPHENIX reactor project, it was necessary to know fission products capture with about 10% accuracy in the fast breeder reactor spectra. In this purpose, integral measurements have been carried out on the main separated products by different experimental technics (oscillation, activation and irradiation methods), but particularly on irradiated fuel pins from RAPSODIE and PHENIX reactors in order to directly obtain total effect of fission products. Same tendencies have been observed for both enriched uranium fuel and LMFBR characteristic plutonium fuel. All experimental results have been introduced in CARNAVAL cross section set [fr

Integral test of JENDL-3.3 on fast reactors

International Nuclear Information System (INIS)

Chiba, Gou; Hazama, Taira

2003-05-01

An integral test has been carried out to evaluate a performance of evaluated nuclear data library JENDL-3.3, which was newly released, in a view of applying neutronics analyses of fast reactors. Japan Nuclear Cycle Development Institute has a large amount of data of critical assembly experiments (ZPPR, BFS, MOZART and FCA) and power reactor tests (JOYO). The database was utilized in this test. In plutonium loaded cores, an improvement was observed about 0.3% ε k in criticality and 5% in the non-leakage term of sodium void reactivity by a revision form JENDL-3.2 to -3.3. These results shoed that the revision is valid in plutonium loaded cores. In uranium loaded cores, dependence of C/E values on control rod position became smaller in control rod worth in ZPPR cores. On the other hand, C/E values became worse both in criticality (0.6%εk) and in sodium void reactivity (30%) in BFS cores. The main cause was a revision of uranium-235 capture cross section, and it could not be concluded whether the revision is valid or not in uranium loaded cores. It is necessary to carry out a validation test at other independent critical experiments in which uranium fuel is used. (author)

Neutron-physical simulation of fast nuclear reactor cores. Investigation of new and emerging nuclear reactor systems

International Nuclear Information System (INIS)

Friess, Friederike Renate

2017-01-01

According to a many publications and discussions, fast reactors hold promises to improve safety, non-proliferation, economic aspects, and reduce the nuclear waste problems. Consequently, several reactor designs advocated by the Generation IV Forum are fast reactors. In reality, however, after decades of research and development and billions of dollars investment worldwide, there are only two fast breeders currently operational on a commercial basis: the Russian reactors BN-600 and BN-800. Energy generation alone is apparently not a sufficient selling point for fast breeder reactors. Therefore, other possible applications for fast nuclear reactors are advocated. Three relevant examples are investigated in this thesis. The first one is the disposition of excess weapon-grade plutonium. Unlike for high enriched uranium that can be downblended for use in light water reactors, there exists no scientifically accepted solution for the disposition of weapon-grade plutonium. One option is the use in fast reactors that are operated for energy production. In the course of burn-up, the plutonium is irradiated which intends to fulfill two objectives: the resulting isotopic composition of the plutonium is less suitable for nuclear weapons, while at the same time the build-up of fission products results in a radiation barrier. Appropriate reprocessing technology is in order to extract the plutonium from the spent fuel. The second application is the use as so-called nuclear batteries, a special type of small modular reactors (SMRs). Nuclear batteries offer very long core lifetimes and have a very small energy output of sometimes only 10 MWe. They can supposedly be placed (almost) everywhere and supply energy without the need for refueling or shuffling of fuel elements for long periods. Since their cores remain sealed for several decades, nuclear batteries are claimed to have a higher proliferation resistance. The small output and the reduced maintenance and operating requirements

Neutron-physical simulation of fast nuclear reactor cores. Investigation of new and emerging nuclear reactor systems

Energy Technology Data Exchange (ETDEWEB)

Friess, Friederike Renate

2017-07-12

According to a many publications and discussions, fast reactors hold promises to improve safety, non-proliferation, economic aspects, and reduce the nuclear waste problems. Consequently, several reactor designs advocated by the Generation IV Forum are fast reactors. In reality, however, after decades of research and development and billions of dollars investment worldwide, there are only two fast breeders currently operational on a commercial basis: the Russian reactors BN-600 and BN-800. Energy generation alone is apparently not a sufficient selling point for fast breeder reactors. Therefore, other possible applications for fast nuclear reactors are advocated. Three relevant examples are investigated in this thesis. The first one is the disposition of excess weapon-grade plutonium. Unlike for high enriched uranium that can be downblended for use in light water reactors, there exists no scientifically accepted solution for the disposition of weapon-grade plutonium. One option is the use in fast reactors that are operated for energy production. In the course of burn-up, the plutonium is irradiated which intends to fulfill two objectives: the resulting isotopic composition of the plutonium is less suitable for nuclear weapons, while at the same time the build-up of fission products results in a radiation barrier. Appropriate reprocessing technology is in order to extract the plutonium from the spent fuel. The second application is the use as so-called nuclear batteries, a special type of small modular reactors (SMRs). Nuclear batteries offer very long core lifetimes and have a very small energy output of sometimes only 10 MWe. They can supposedly be placed (almost) everywhere and supply energy without the need for refueling or shuffling of fuel elements for long periods. Since their cores remain sealed for several decades, nuclear batteries are claimed to have a higher proliferation resistance. The small output and the reduced maintenance and operating requirements

Swiss R and D on uranium-free LWR fuels for plutonium incineration

International Nuclear Information System (INIS)

Stanculescu, A.; Chawla, R.; Degueldre, C.; Kasemeyer, U.; Ledergerber, G.; Paratte, J.M.

1999-01-01

The most efficient way to enhance the plutonium consumption in LWRs is to eliminate plutonium production altogether. This requirement leads to fuel concepts in which the uranium is replaced by an inert matrix. The inert matrix material studied at PSI is zirconium oxide. For reactivity control reasons, adding a burnable poison to this fuel proves to be necessary. The studies performed at PSI have identified erbium oxide as the most suitable candidate for this purpose. With regard to material technology aspects, efforts have concentrated on the evaluation of fabrication feasibility and on the determination of the physicochemical properties of the chosen single phase zirconium/ erbium/plutonium oxide material stabilised as a cubic solution by yttrium. The results to-date, obtained for inert matrix samples containing thorium or cerium as plutonium substitute, confirm the robustness and stability of this material. With regard to reactor physics aspects, our studies indicate the feasibility of uranium-free, plutonium-fuelled cores having operational characteristics quite similar to those of conventional UO 2 -fuelled ones, and much higher plutonium consumption rates, as compared to 100% MOX loadings. The safety features of such cores, based on results obtained from static neutronics calculations, show no cliff edges. However, the need for further detailed transient analyses is clearly recognised. Summarising, PSI's studies indicate the feasibility of a uranium-free plutonium fuel to be considered in 'maximum plutonium consumption LWRs' operating in a 'once-through' mode. With regard to reactor physics, future efforts will concentrate on strengthening the safety case of uranium-free cores, as well as on improving the integral data base for validation of the neutronics calculations. Material technology studies will be continued to investigate the physico-chemical properties of the inert matrix fuel containing plutonium and will focus on the planning and evaluation of

Burn-up measurements on nuclear reactor fuels using high performance liquid chromatography

International Nuclear Information System (INIS)

Sivaraman, N.; Subramaniam, S.; Srinivasan, T.G.; Vasudeva Rao, P.R.

2002-01-01

Burn-up measurements on thermal as well as fast reactor fuels were carried out using high performance liquid chromatography (HPLC). A column chromatographic technique using di-(2-ethylhexyl) phosphoric acid (HDEHP) coated column was employed for the isolation of lanthanides from uranium, plutonium and other fission products. Ion-pair HPLC was used for the separation of individual lanthanides. The atom percent fissions were calculated from the concentrations of the lanthanide (neodymium in the case of thermal reactor and lanthanum for the fast reactor fuels) and from uranium and plutonium contents of the dissolver solutions. The HPLC method was also used for determining the fractional fissions from uranium and plutonium for the thermal reactor fuel. (author)

A solvent proceed for the extraction of the irradiate uranium and plutonium in the reactor core; Un procede par solvant pour l'extraction du plutonium de l'uranium irradie dans les piles

Energy Technology Data Exchange (ETDEWEB)

Goldschmidt, B; Regnaut, P; Prevot, I [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1955-07-01

Description of the conditions of plutonium, fission products and of uranium separation by selective extraction of the nitrates by organic solvent, containing a simultaneous extraction of plutonium and uranium, followed by a plutonium re-extraction after reduction, and an uranium re-extraction. The rates of decontamination being insufficient in this first stage, we also describes the processes of decontamination permitting separately to get the rates wanted for uranium and plutonium. Finally, we describes the beginning of the operation that consists in a nitric dissolution of the active uranium while capturing the products of gaseous fission, as well as the final concentration of the products of fission in a concentrated solution. (authors) [French] Description des conditions de separation du plutonium, des produits de fission et de l'uranium au moyen d'une extraction selective des nitrates par solvant organique, comprenant une extraction simultanee du plutonium et de l'uranium, suivie d'une reextraction du plutonium apres reduction, et d'une reextraction de l'uranium. Les taux de decontamination etant insuffisants dans ce premier stade, on decrit egalement les processus de decontamination permettant separement d'obtenir les taux desires pour l'uranium et le plutonium. Enfin, on decrit aussi le debut de l'operation qui consiste en une dissolution nitrique de l'uranium actif en captant les produits de fission gazeux, ainsi que la concentration finale des produits de fission sous forme de solution concentree. (auteurs)

Evolution of the technical concept of fast reactors. The concept of BREST

International Nuclear Information System (INIS)

Orlov, V.V.

2001-01-01

Having understood that conventional power was limited by available fuel resources, as well as the environmental concern, and willing to use the advantages of defense nuclear power achievements, the development of civil nuclear power was initiated. Scarce supply of uranium has been a matter of concern from the very beginning of nuclear power development, but plutonium produced in the thermal reactors was supposed to be used as fuel for the fast reactors which would not be limited by fuel resources. In order to attain high breeding ratio and high power density, the first generation of fast reactors were designed with sodium coolant, uranium blanket to make up for a decrease in breeding ratio if uranium oxides were used as fuel. Development of nuclear power in the sixties and seventies was followed by stagnation. Lessons learned from a 50-year experience and new conditions set for power industry demand a new concept of fast reactor which would meet a variety of cost-efficiency and safety requirements in their present understanding. Development of fast breeders in Russia began after commissioning of BN-350 and completion of BN-600 design. According to present demands BREST reactors should be designed so as to implement consistently the principles of natural safety without deviation from materials and technology which was proven in defense and civil nuclear power facilities

Recycling of plutonium and uranium in water reactor fuel. Proceedings of a technical committee meeting

International Nuclear Information System (INIS)

1997-05-01

The Technical Committee Meeting on Recycling of Plutonium and Uranium in Water Reactor Fuel was recommended by the International Working Group on Fuel Performance and Technology (IWGFPT). Its aim was to obtain an overall picture of MOX fabrication capacity and technology, actual performance of this kind of fuel, and ways explored to dispose of the weapons grade plutonium. The subject of this meeting had been reviewed by the International Atomic Energy Agency every 5 to 6 years and for the first time the problem of weapons grade plutonium disposal was included. The papers presented provide a summary of experience on MOX fuel and ongoing research in this field in the participating countries. The meeting was hosted by British Nuclear Fuels plc, at Newby Bridge, United Kingdom, from 3 to 7 July 1995. Fifty-six participants from twelve countries or international organizations took part. Refs, figs, tabs

Chapter 1. General information about uranium. 1.10. Uranium application

International Nuclear Information System (INIS)

Khakimov, N.; Nazarov, Kh.M.; Mirsaidov, I.U.

2011-01-01

Full text: Metallic uranium or its compounds are used as nuclear fuel in nuclear reactors. A natural or low-enriched admixture of uranium isotopes is applied in stationery reactors of nuclear power plants, and products of a high enrichment degree are used in nuclear power plants or in reactors that operates with fast neutrons. 235 U is a source of nuclear energy in nuclear weapons. Depleted uranium is used as armour-piercing core in bombshells. 238 U serves as a source of secondary nuclear fuel - plutonium. (author)

Chapter 1. General information about uranium. 1.10. Uranium application

International Nuclear Information System (INIS)

Khakimov, N.; Nazarov, Kh.M.; Mirsaidov, I.U.

2012-01-01

Full text: Metallic uranium or its compounds are used as nuclear fuel in nuclear reactors. A natural or low-enriched admixture of uranium isotopes is applied in stationery reactors of nuclear power plants, and products of a high enrichment degree are used in nuclear power plants or in reactors that operates with fast neutrons. 235 U is a source of nuclear energy in nuclear weapons. Depleted uranium is used as armour-piercing core in bombshells. 238 U serves as a source of secondary nuclear fuel - plutonium.

Material unaccounted for at the Southwest Experimental Fast Oxide Reactor: The SEFOR MUF

International Nuclear Information System (INIS)

Higinbotham, W.A.

1994-01-01

The U.S. Atomic Energy Commission contracted with the General Electric Company to design, construct, and operate the Southwest Experimental Fast Oxide Reactor (SEFOR) to measure the Doppler effect for fast neutron breeder reactors. It contracted with Nuclear Fuel Services to fabricate the fuel rods for the reactor. When the reactor went critical in May, 1969, it appeared that some of the mixed uranium-plutonium oxide (MOX) fuel rods did not contain the specified quantity of plutonium. The SEFOR operators soon found several fuel rods which appeared to be low in plutonium. The safeguards group at Brookhaven was asked to look into the problem and, if possible, determine how much plutonium was missing from the unirradiated rods and from the larger number which had been slightly irradiated in the reactor. It was decided that the plutonium content of the unirradiated and irradiated rods could be measured relative to a reference rod using a high resolution gamma-ray detector and also by neutron measurements using an auto-correlation circuit recently developed at the Naval Research Laboratory (NRL). During the next two years, Brookhaven personnel and C.V. Strain of NRL made several trips to the SEFOR reactor. About 250 of the 775 rods were measured by two or more methods, using a sodium-iodide detector, a high-resolution germanium detector, a neutron detector, or the reactor (to measure reactivity). The research team concluded that 4.6 ± 0.46 kg of plutonium was missing out of the 433 kg that the rods should have contained. This report describes the SEFOR experiment and the procedures used to determine the material unaccounted for, or MUF

Proposed fuel cycle for the Integral Fast Reactor

International Nuclear Information System (INIS)

Burris, L.; Walters, L.C.

1985-01-01

One of the key features of ANL's Integral Fast Reactor (IFR) concept is a close-coupled fuel cycle. The proposed fuel cycle is similar to that demonstrated over the first five to six years of operation of EBR-II, when a fuel cycle facility adjacent to EBR-II was operated to reprocess and refabricate rapidly fuel discharged from the EBR-II. Locating the IFR and its fuel cycle facility on the same site makes the IFR a self-contained system. Because the reactor fuel and the uranium blanket are metals, pyrometallurgical processes (shortned to ''pyroprocesses'') have been chosen. The objectives of the IFR processes for the reactor fuel and blanket materials are to (1) recover fissionable materials in high yield; (2) remove fission products adequately from the reactor fuel, e.g., a decontamination factor of 10 to 100; and (3) upgrade the concentration of plutonium in uranium sufficiently to replenish the fissile-material content of the reactor fuel. After the fuel has been reconstituted, new fuel elements will be fabricated for recycle to the reactor

The U.S.-Russian joint studies on using power reactors to disposition surplus weapons plutonium as spent fuel

International Nuclear Information System (INIS)

Chebeskov, A.; Kalashnikov, A.; Pavlovichev, A.

1997-09-01

In 1996, the US and the Russian Federation completed an initial joint study of the candidate options for the disposition of surplus weapons plutonium in both countries. The options included long term storage, immobilization of the plutonium in glass or ceramic for geologic disposal, and the conversion of weapons plutonium to spent fuel in power reactors. For the latter option, the US is only considering the use of existing light water reactors (LWRs) with no new reactor construction for plutonium disposition, or the use of Canadian deuterium uranium (CANDU) heavy water reactors. While Russia advocates building new reactors, the cost is high, and the continuing joint study of the Russian options is considering only the use of existing VVER-1000 LWRs in Russia and possibly Ukraine, the existing BN-60O fast neutron reactor at the Beloyarsk Nuclear Power Plant in Russia, or the use of the Canadian CANDU reactors. Six of the seven existing VVER-1000 reactors in Russia and the eleven VVER-1000 reactors in Ukraine are all of recent vintage and can be converted to use partial MOX cores. These existing VVER-1000 reactors are capable of converting almost 300 kg of surplus weapons plutonium to spent fuel each year with minimum nuclear power plant modifications. Higher core loads may be achievable in future years

Hot pressing of uranium nitride and mixed uranium plutonium nitride

International Nuclear Information System (INIS)

Chang, J.Y.

1975-01-01

The hot pressing characteristics of uranium nitride and mixed uranium plutonium nitride were studied. The utilization of computer programs together with the experimental technique developed in the present study may serve as a useful purpose of prediction and fabrication of advanced reactor fuel and other high temperature ceramic materials for the future. The densification of nitrides follow closely with a plastic flow theory expressed as: d rho/ dt = A/T(t) (1-rho) [1/1-(1-rho)/sup 2/3/ + B1n (1-rho)] The coefficients, A and B, were obtained from experiment and computer curve fitting. (8 figures) (U.S.)

Fast reactor fuel reprocessing in the UK

International Nuclear Information System (INIS)

Allardice, R.H.; Williams, J.; Buck, C.

1977-01-01

Enriched uranium metal fuel irradiated in the Dounreay Fast Reactor has been reprocessed and refabricated in plants specifically designed for the purpose in the U.K. since 1961. Efficient and reliable fuel recycle is essential to the development of a plutonium based fast reactor system and the importance of establishing at an early stage fast reactor fuel reprocessing has been reinforced by current world difficulties in reprocessing high burn-up thermal reactor oxide fuel. In consequence, the U.K. has decided to reprocess irradiated fuel from the 250 MW(E) Prototype Fast Reactor as an integral part of the fast reactor development programme. Flowsheet and equipment development work for the small scale fully active demonstration plant have been carried out over the past 5 years and the plant will be commissioned and ready for active operation during 1977. In parallel, a comprehensive waste management system has been developed and installed. Based on this development work and the information which will arise from active operation of the plant a parallel development programme has been initiated to provide the basis for the design of a large scale fast reactor fuel reprocessing plant to come into operation in the late 1980s to support the projected U.K. fast reactor installation programme. The paper identifies the important differences between fast reactor and thermal reactor fuel reprocessing technologies and describes some of the development work carried out in these areas for the small scale P.F.R. fuel reprocessing operation. In addition, the development programme in aid of the design of a larger scale fast reactor fuel reprocessing plant is outlined and the current design philosophy is discussed

Advanced Safeguards Approaches for New Fast Reactors

International Nuclear Information System (INIS)

Durst, Philip C.; Therios, Ike; Bean, Robert; Dougan, A.; Boyer, Brian; Wallace, Rick L.; Ehinger, Michael H.; Kovacic, Don N.; Tolk, K.

2007-01-01

This third report in the series reviews possible safeguards approaches for new fast reactors in general, and the ABR in particular. Fast-neutron spectrum reactors have been used since the early 1960s on an experimental and developmental level, generally with fertile blanket fuels to 'breed' nuclear fuel such as plutonium. Whether the reactor is designed to breed plutonium, or transmute and 'burn' actinides depends mainly on the design of the reactor neutron reflector and the whether the blanket fuel is 'fertile' or suitable for transmutation. However, the safeguards issues are very similar, since they pertain mainly to the receipt, shipment and storage of fresh and spent plutonium and actinide-bearing 'TRU'-fuel. For these reasons, the design of existing fast reactors and details concerning how they have been safeguarded were studied in developing advanced safeguards approaches for the new fast reactors. In this regard, the design of the Experimental Breeder Reactor-II 'EBR-II' at the Idaho National Laboratory (INL) was of interest, because it was designed as a collocated fast reactor with a pyrometallurgical reprocessing and fuel fabrication line--a design option being considered for the ABR. Similarly, the design of the Fast Flux Facility (FFTF) on the Hanford Site was studied, because it was a successful prototype fast reactor that ran for two decades to evaluate fuels and the design for commercial-scale fast reactors

CANDU reactors with reactor grade plutonium/thorium carbide fuel

Energy Technology Data Exchange (ETDEWEB)

Sahin, Suemer [Atilim Univ., Ankara (Turkey). Faculty of Engineering; Khan, Mohammed Javed; Ahmed, Rizwan [Pakistan Institute of Engineering and Applied Sciences, Islamabad (Pakistan); Gazi Univ., Ankara (Turkey). Faculty of Technology

2011-08-15

Reactor grade (RG) plutonium, accumulated as nuclear waste of commercial reactors can be re-utilized in CANDU reactors. TRISO type fuel can withstand very high fuel burn ups. On the other hand, carbide fuel would have higher neutronic and thermal performance than oxide fuel. In the present work, RG-PuC/ThC TRISO fuels particles are imbedded body-centered cubic (BCC) in a graphite matrix with a volume fraction of 60%. The fuel compacts conform to the dimensions of sintered CANDU fuel compacts are inserted in 37 zircolay rods to build the fuel zone of a bundle. Investigations have been conducted on a conventional CANDU reactor based on GENTILLYII design with 380 fuel bundles in the core. Three mixed fuel composition have been selected for numerical calculation; (1) 10% RG-PuC + 90% ThC; (2) 30% RG-PuC + 70% ThC; (3) 50% RG-PuC + 50% ThC. Initial reactor criticality values for the modes (1), (2) and (3) are calculated as k{sub {infinity}}{sub ,0} = 1.4848, 1.5756 and 1.627, respectively. Corresponding operation lifetimes are {proportional_to} 2.7, 8.4, and 15 years and with burn ups of {proportional_to} 72 000, 222 000 and 366 000 MW.d/tonne, respectively. Higher initial plutonium charge leads to higher burn ups and longer operation periods. In the course of reactor operation, most of the plutonium will be incinerated. At the end of life, remnants of plutonium isotopes would survive; and few amounts of uranium, americium and curium isotopes would be produced. (orig.)

Assessment of Startup Fuel Options for a Test or Demonstration Fast Reactor

Energy Technology Data Exchange (ETDEWEB)

Carmack, Jon [Idaho National Lab. (INL), Idaho Falls, ID (United States); Hayes, Steven [Idaho National Lab. (INL), Idaho Falls, ID (United States); Walters, L. C. [Idaho National Lab. (INL), Idaho Falls, ID (United States)

2015-09-01

This document explores startup fuel options for a proposed test/demonstration fast reactor. The fuel options considered are the metallic fuels U-Zr and U-Pu-Zr and the ceramic fuels UO₂ and UO₂-PuO₂ (MOX). Attributes of the candidate fuel choices considered were feedstock availability, fabrication feasibility, rough order of magnitude cost and schedule, and the existing irradiation performance database. The reactor-grade plutonium bearing fuels (U-Pu-Zr and MOX) were eliminated from consideration as the initial startup fuels because the availability and isotopics of domestic plutonium feedstock is uncertain. There are international sources of reactor grade plutonium feedstock but isotopics and availability are also uncertain. Weapons grade plutonium is the only possible source of Pu feedstock in sufficient quantities needed to fuel a startup core. Currently, the available U.S. source of (excess) weapons-grade plutonium is designated for irradiation in commercial light water reactors (LWR) to a level that would preclude diversion. Weapons-grade plutonium also contains a significant concentration of gallium. Gallium presents a potential issue for both the fabrication of MOX fuel as well as possible performance issues for metallic fuel. Also, the construction of a fuel fabrication line for plutonium fuels, with or without a line to remove gallium, is expected to be considerably more expensive than for uranium fuels. In the case of U-Pu-Zr, a relatively small number of fuel pins have been irradiated to high burnup, and in no case has a full assembly been irradiated to high burnup without disassembly and re-constitution. For MOX fuel, the irradiation database from the Fast Flux Test Facility (FFTF) is extensive. If a significant source of either weapons-grade or reactor-grade Pu became available (i.e., from an international source), a startup core based on Pu could be reconsidered.

Diffusion in the uranium - plutonium system and self-diffusion of plutonium in epsilon phase; Diffusion dans le systeme uranium-plutonium et autodiffusion du plutonium epsilon

Energy Technology Data Exchange (ETDEWEB)

Dupuy, M [Commissariat a l' Energie Atomique, Fontenay-Aux-Roses (France). Centre d' Etudes Nucleaires

1967-07-01

A survey of uranium-plutonium phase diagram leads to confirm anglo-saxon results about the plutonium solubility in {alpha} uranium (15 per cent at 565 C) and the uranium one in {zeta} phase (74 per cent at 565 C). Interdiffusion coefficients, for concentration lower than 15 per cent had been determined in a temperature range from 410 C to 640 C. They vary between 0.2 and 6 10{sup 12} cm{sup 2} s{sup -1}, and the activation energy between 13 and 20 kcal/mole. Grain boundary, diffusion of plutonium in a uranium had been pointed out by micrography, X-ray microanalysis and {alpha} autoradiography. Self-diffusion of plutonium in {epsilon} phase (bcc) obeys Arrhenius law: D = 2. 10{sup -2} exp -(18500)/RT. But this activation energy does not follow empirical laws generally accepted for other metals. It has analogies with 'anomalous' bcc metals ({beta}Zr, {beta}Ti, {beta}Hf, U{sub {gamma}}). (author) [French] Une etude du diagramme d'equilibre uranium-plutonium conduit a confirmer les resultats anglo-saxons relatifs a la solubilite du plutonium dans l'uranium {alpha} (15 pour cent a 565 C) et de l'uranium dans la phase {zeta} (74 pour cent a 565 C). Les coefficients de diffusion chimique, pour des concentrations inferieures a 15 pour cent ont ete determines a des temperatures comprises entre 410 et 640 C. Ils se situent entre 0.2 et 6. 10{sup 12} cm{sup 2} s{sup -1}. L'energie d'activation varie entre 13 et 20 kcal/mole. La diffusion intergranulaire du plutonium dans l'uranium a a ete mise en evidence par micrographie, microanalyse X et autoradiographie {alpha}. L' autodiffusion du plutonium {beta} cubique centree obeit a la loi d'Arrhenius D = 2. 10{sup -2} exp - (18500)/RT. Son energie d'activation n'obeit pas aux lois empiriques generalement admises pour les autres metaux. Elle possede des analogies avec les cubiques centres ''anormaux'' (Zr{beta}, Ti{beta}, Hf{beta}, U{gamma}). (auteur)

Mixed Uranium/Refractory Metal Carbide Fuels for High Performance Nuclear Reactors

International Nuclear Information System (INIS)

Knight, Travis; Anghaie, Samim

2002-01-01

Single phase, solid-solution mixed uranium/refractory metal carbides have been proposed as an advanced nuclear fuel for advanced, high-performance reactors. Earlier studies of mixed carbides focused on uranium and either thorium or plutonium as a fuel for fast breeder reactors enabling shorter doubling owing to the greater fissile atom density. However, the mixed uranium/refractory carbides such as (U, Zr, Nb)C have a lower uranium densities but hold significant promise because of their ultra-high melting points (typically greater than 3700 K), improved material compatibility, and high thermal conductivity approaching that of the metal. Various compositions of (U, Zr, Nb)C were processed with 5% and 10% metal mole fraction of uranium. Stoichiometric samples were processed from the constituent carbide powders, while hypo-stoichiometric samples with carbon-to-metal (C/M) ratios of 0.92 were processed from uranium hydride, graphite, and constituent refractory carbide powders. Processing techniques of cold uniaxial pressing, dynamic magnetic compaction, sintering, and hot pressing were investigated to optimize the processing parameters necessary to produce high density (low porosity), single phase, solid-solution mixed carbide nuclear fuels for testing. This investigation was undertaken to evaluate and characterize the performance of these mixed uranium/refractory metal carbides for high performance, ultra-safe nuclear reactor applications. (authors)

Advanced Safeguards Approaches for New Fast Reactors

Energy Technology Data Exchange (ETDEWEB)

Durst, Philip C.; Therios, Ike; Bean, Robert; Dougan, A.; Boyer, Brian; Wallace, Rick L.; Ehinger, Michael H.; Kovacic, Don N.; Tolk, K.

2007-12-15

This third report in the series reviews possible safeguards approaches for new fast reactors in general, and the ABR in particular. Fast-neutron spectrum reactors have been used since the early 1960s on an experimental and developmental level, generally with fertile blanket fuels to “breed” nuclear fuel such as plutonium. Whether the reactor is designed to breed plutonium, or transmute and “burn” actinides depends mainly on the design of the reactor neutron reflector and the whether the blanket fuel is “fertile” or suitable for transmutation. However, the safeguards issues are very similar, since they pertain mainly to the receipt, shipment and storage of fresh and spent plutonium and actinide-bearing “TRU”-fuel. For these reasons, the design of existing fast reactors and details concerning how they have been safeguarded were studied in developing advanced safeguards approaches for the new fast reactors. In this regard, the design of the Experimental Breeder Reactor-II “EBR-II” at the Idaho National Laboratory (INL) was of interest, because it was designed as a collocated fast reactor with a pyrometallurgical reprocessing and fuel fabrication line – a design option being considered for the ABR. Similarly, the design of the Fast Flux Facility (FFTF) on the Hanford Site was studied, because it was a successful prototype fast reactor that ran for two decades to evaluate fuels and the design for commercial-scale fast reactors.

Physics studies of weapons plutonium disposition in the Integral Fast Reactor closed fuel cycle

International Nuclear Information System (INIS)

Hill, R.N.; Wade, D.C.; Liaw, J.R.; Fujita, E.K.

1995-01-01

The core performance impact of weapons plutonium introduction into the Integral Fast Reactor (IFR) closed fuel cycle is investigated by comparing three disposition scenarios: a power production mode, a moderate destruction mode, and a maximum destruction mode, all at a constant heat rating of 840 MW(thermal). For each scenario, two fuel cycle models are evaluated: cores using weapons material as the sole source of transuranics in a once-through mode and recycle cores using weapons material only as required for a makeup feed. In addition, the impact of alternative feeds (recycled light water reactor or liquid-metal reactor transuranics) on burner core performance is assessed. Calculated results include mass flows, detailed isotopic distributions, neutronic performance characteristics, and reactivity feedback coefficients. In general, it is shown that weapons plutonium does not have an adverse effect on IFR core performance characteristics; also, favorable performance can be maintained for a wide variety of feed materials and fuel cycle strategies

Effect of the plutonium isotopic composition on the performance of fast reactors; Effet de la composition isotopique du plutonium sur le rendement de reacteurs a neutrons rapides; Vliyanie izotopnogo sostava plutoniya na rabotu reaktorov na bystrykh nejtronakh; Efectos de la composicion isotopica del plutonio sobre el funcionamiento de los reactores rapidos

Energy Technology Data Exchange (ETDEWEB)

Yiftah, S [Israel Atomic Energy Commission (Israel)

1962-03-15

The isotopic composition of plutonium to be used as fuel for fast reactors will depend on the source of plutonium. In principle three different sources are possible: (a) production reactors; (6) thermal power reactors (using natural uranium or enriched uranium as fuel); (c) fast reactor blankets. In general, source (a) and to some extent source (c) will provide relatively 'clean' plutonium, that is mostly Pu{sup 239}, while plutonium from source (6) will be 'dirty' plutonium, that is plutonium rich in Pu{sup 240}, Pu{sup 241}, and Pu{sup 242}. The degree of 'dirtiness' will depend on the kind of reactor, amount of burn-up and in general on the irradiation history of the fuel. The question then arises, can one use as fuel for fast reactors any kind of plutonium? To investigate the effect of different isotopic composition of the plutonium fuel, in the metallic, oxide and carbide form, on the performance of fast reactors, a limited series of spherical geometry 16-group diffusion theory calculations were performed, using the 16-group cross-section set developed recently by Yiftah, Okrent and Moldauer and taking three different kinds of plutonium, starting with pure Pu{sup 239} and increasing the amount of higher isotopes. For the systems studied-800, 1500 and 2500-l core-volumes, which are typical for large fast power reactors-the result is, when one takes into account only the thermally fissionable isotopes Pu{sup 239} arid Pu{sup 241}, that the 'dirtier' the plutonium, the smaller the critical mass and the higher the breeding ratio. For the 1500-l reactor, taken as an example, it is further found that in the metallic, oxide and carbide plutonium fuels the reactivity change upon removal of 40% of the sodium initially present in the core is made more negative (or less positive) when the plutonium is richer in higher isotopes. (author) [French] La composition isotopique du plutonium qui doit etre utilise comme combustible dans des reacteurs a neutrons rapides depend de

ZZ WPPR-FR-MOX/BNCMK, Benchmark on Pu Burner Fast Reactor

International Nuclear Information System (INIS)

Garnier, J.C.; Ikegami, T.

1993-01-01

Description of program or function: In order to intercompare the characteristics of the different reactors considered for Pu recycling, in terms of neutron economy, minor actinide production, uranium content versus Pu burning, the NSC Working Party on Physics of Plutonium Recycling (WPPR) is setting up several benchmark studies. They cover in particular the case of the evolution of the Pu quality and Pu fissile content for Pu recycling in PWRs; the void coefficient in PWRs partly fuelled with MOX versus Pu content; the physics characteristics of non-standard fast reactors with breeding ratios around 0.5. The following benchmarks are considered here: - Fast reactors: Pu Burner MOX fuel, Pu Burner metal fuel; - PWRs: MOX recycling (bad quality Pu), Multiple MOX recycling

Fabrication of Fast Reactor Fuel Pins for Test Irradiations

Energy Technology Data Exchange (ETDEWEB)

Karsten, G. [Institute for Applied Reactor Physics, Kernforschungszentrum Karlsruhe, Karlsruhe, Federal Republic of Germany (Germany); Dippel, T. [Institute for Radiochemistry, Kernforschungszentrum Karlsruhe, Karlsruhe, Federal Republic of Germany (Germany); Laue, H. J. [Institute for Applied Reactor Physics, Kernforschungszentrum Karlsruhe, Karlsruhe, Federal Republic of Germany (Germany)

1967-09-15

An extended irradiation programme is being carried out for the fuel element development of the Karlsruhe fast breeder project. A very important task within the programme is the testing of plutonium-containing fuel pins in a fast-reactor environment. This paper deals with fabrication of such pins by our laboratories at Karlsruhe. For the fast reactor test positions at present envisaged a fuel with 15% plutonium and the uranium fully enriched is appropriate. Hie mixed oxide is both pelletized and vibro-compacted with smeared densities between 80 and 88% theoretical. The pin design is, for example, such that there are two gas plena at the top and bottom, and one blanket above the fuel with the fuel zone fitting to the test reactor core length. The specifications both for fuel and cladding have been adapted to the special purpose of a fast-breeder reactor - the outer dimensions, the choice of cladding and fuel types, the data used and the kind of tests outline the targets of the development. The fuel fabrication is described in detail, and also the powder line used for vibro-compaction. The source materials for the fuel are oxalate PuO{sub 2} and UO{sub 2} from the UF{sub 6} process. The special problems of mechanical mixing and of plutonium homogeneity have been studied. The development of the sintering technique and grain characteristics for vibratory compactive fuel had to overcome serious problems in order to reach 82-83% theoretical. The performance of the pin fabrication needed a major effort in welding, manufacturing of fits and decontamination of the pin surfaces. This was a stimulation for the development of some very subtle control techniques, for example taking clear X-ray photographs and the tube testing. In general the selection of tests was a special task of the production routine. In conclusion the fabrication of the pins resulted in valuable experiences for the further development of fast reactor fuel elements. (author)

Waste management in IFR [Integral Fast Reactor] fuel cycle

International Nuclear Information System (INIS)

Johnson, T.R.; Battles, J.E.

1991-01-01

The fuel cycle of the Integral Fast Reactor (IFR) has important potential advantage for the management of high-level wastes. This sodium-cooled, fast reactor will use metal fuels that are reprocessed by pyrochemical methods to recover uranium, plutonium, and the minor actinides from spent core and blanket fuel. More than 99% of all transuranic (TRU) elements will be recovered and returned to the reactor, where they are efficiently burned. The pyrochemical processes being developed to treat the high-level process wastes are capable of producing waste forms with low TRU contents, which should be easier to dispose of. However, the IFR waste forms present new licensing issues because they will contain chloride salts and metal alloys rather than glass or ceramic. These fuel processing and waste treatment methods can also handle TRU-rich materials recovered from light-water reactors and offer the possibility of efficiently and productively consuming these fuel materials in future power reactors

Possible future roles for fast breeder reactors Part 1 and 2

International Nuclear Information System (INIS)

1978-06-01

Part 1. The Fast Breeder Reactor (in particular in its sodium cooled version) has been steadily developed in the Community. This report attempts to quantify the advantages of this system in terms of fossil energy and uranium savings in the medium/long term as well as to examine some long term economic implications. The methodology of comparing scenarios, not individual reactor systems is followed. These scenarios have been chosen taking into account a range of assumptions concerning Community energy demand growth, fossil energy and uranium availability and technological capabilities. Part 2. The fast breeder reactor (FBR), particularly its sodium-cooled form (LMFBR) has been under development in the Community for many years. Industrial enterprises dedicated to its commercialisation have been formed and long range plans for its industrial utilisation are being formulated. The value of breeder reactors from the point of view of minimising Community fuel requirements has been discussed in Part I of this report (1). In Part II the consequences of delaying their introduction, and the demands placed upon the recycle industry by the introduction of fast reactors of different characteristics, using the Community electricity demand scenarios developed for Part I, are discussed. In addition comments are provided upon the effect of FBR introduction on the size of plutonium stocks

History of fast reactor development in U.S.A.-I

International Nuclear Information System (INIS)

Ninokata, Hisashi; Sasao, Nobuyki

2007-01-01

History and present state of fast reactor was reviewed in series. As a history of fast reactor development in U.S.A. - I, this third lecture presented the dawn of the fast reactor development in the USA. The first fast reactor was the Clementine reactor with plutonium fuels and mercury coolant. The LAMPRE-1 reactor was the first sodium cooled and molten plutonium reactor. Experimental breeder reactor (EBR-1) was the first reactor to produce electricity and four kinds of fuels were loaded. Zero-power reactors were constructed to conduct reactor physics experiments on fast reactors. Today there are renewed interests in fast reactors due to their ability to fission actinides and reduce radioactive wastes. (T. Tanaka)

Civil plutonium in the world: an estimate by the code REACTOR

International Nuclear Information System (INIS)

Braet, J.; Carchon, R.; Van der Meer, K.

1996-11-01

The computer code REACTOR that was developed by the Belgian Nuclear Research Centre SCK/CEN to study the built-up of plutonium stockpiles in the world is described. The code consists of a central database, containing general information about most commercial civil nuclear facilities. Using this code, an overview is given of the evolution of the nuclear energy production in the world, in the past and the medium term future. The nuclear energy production results in the accumulation of spent fuel stocks, containing vast amounts of energy enclosed in the plutonium. The presence and built-up of large stockpiles of spent fuel and separated plutonium originating from the civil fuel cycle is estimated. In this report several possible scenarios are considered for the use of that plutonium, with the aim of minimizing those stocks. According to the different national policies, scenarios such as open fuel cycle, thermal reactors or fast reactor cycle with the burning of plutonium in fast reactors are envisaged

Development of alternate extractant systems for fast reactor fuel cycle

International Nuclear Information System (INIS)

Vasudeva Rao, P.R.; Suresh, A.; Venkatesan, K.A.; Srinivasan, T.G.; Raj, Baldev

2007-01-01

Due to the limitations of TBP in processing of high burn-up, Pu-rich fast reactor fuels, there is a need to develop alternate extractants for fast reactor fuel processing. In this context, our Centre has been examining the suitability of alternate tri-alkyl phosphates. Third phase formation in the extraction of Th(IV) by TBP, tri-n-amyl phosphate (TAP) and tri-2-methyl-butyl phosphate (T2MBP) from nitric acid media has been investigated under various conditions to derive conclusions on their application for extraction of Pu at macro levels. The chemical and radiolytic degradation of tri-n-amyl-phosphate (TAP) diluted in normal paraffin hydrocarbon (NPH) in the presence of nitric acid has been investigated by the measurement of plutonium retention in organic phase. The potential application of room temperature ionic liquids (RTILs) for reprocessing of spent nuclear fuel has been explored. Extraction of uranium (VI) and palladium (II) from nitric acid medium by commercially available RTIL and tri-n-butyl phosphate solution in RTIL have been studied and the feasibility of electrodeposition of uranium as uranium oxide (UO 2 ) and palladium (II) as metallic palladium from the loaded organic phase have been demonstrated. This paper describes results of the above studies and discusses the suitability of the systems for fast reactor fuel reprocessing. (authors)

General consideration of effective plutonium utilization in future LWRs

International Nuclear Information System (INIS)

Ishikawa, Nobuyuki; Okubo, Tsutomu

2009-01-01

In this study, the potential of mixed oxide fueled light water reactors (MOX-LWRs), especially focusing on the high conversion type LWRs (HC-LWRs) such as FLWR are evaluated in terms of both economic aspect and effective use of plutonium. For economics consideration, relative economics positions of MOX-LWRs are clarified comparing the cost of electricity for uranium fueled LWRs (U-LWRs), MOX-LWRs and fast breeder reactors (FBRs) assuming future natural uranium price raise and variation of parameters such as construction cost and capacity factor. Also the economic superiority of MOX utilization against the uranium use is mentioned from the view point of plutonium credit concerning to the front-end fuel cycle cost. In terms of effective use of plutonium, comparative evaluations on plutonium mass balance in the cases of HC-LWR and high moderation type LWRs (HM-LWRs) taking into account plutonium quality (ratio of fissile to total plutonium) constraint in multiple recycling are performed as representative MOX utilization cases. Through this evaluation, the advantageous features of plutonium multiple recycling by HC-LWR are clarified. From all these results, merits of the introduction of HC-LWRs are discussed. (author)

Fast-reactor fuel reprocessing in the United Kingdom

International Nuclear Information System (INIS)

Allardice, R.H.; Buck, C.; Williams, J.

1977-01-01

Enriched uranium metal fuel irradiated in the Dounreay Fast Reactor has been reprocessed and refabricated in plants specifically designed for the purpose in the United Kingdom since 1961. Efficient and reliable fuel recycle is essential to the development of a plutonium-based fast-reactor system, and the importance of establishing at an early stage fast-reactor fuel reprocessing has been reinforced by current world difficulties in reprocessing high-burnup thermal-reactor oxide fuel. The United Kingdom therefore decided to reprocess irradiated fuel from the 250MW(e) Prototype Fast Reactor (PFR) as an integral part of the fast reactor development programme. Flowsheet and equipment development work for the small-scale fully active demonstration plant has been carried out since 1972, and the plant will be commissioned and ready for active operation during 1977. In parallel, a comprehensive waste-management system has been developed and installed. Based on this development work and the information which will arise from active operation of the plant, a parallel development programme has been initiated to provide the basis for the design of a large-scale fast-reactor fuel-reprocessing plant to come into operation in the late 1980s to support the projected UK fast-reactor installation programme. The paper identifies the important differences between fast-reactor and thermal-reactor fuel-reprocessing technologies and describes some of the development work carried out in these areas for the small-scale PFR fuel-reprocessing operation. In addition, the development programme in aid of the design of a larger scale fast-reactor fuel-reprocessing plant is outlined and the current design philosophy discussed. (author)

Separation of Plutonium from Irradiated Fuels and Targets

Energy Technology Data Exchange (ETDEWEB)

Gray, Leonard W. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Holliday, Kiel S. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Murray, Alice [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Thompson, Major [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Thorp, Donald T. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Yarbro, Stephen [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Venetz, Theodore J. [Hanford Site, Benton County, WA (United States)

2015-09-30

Spent nuclear fuel from power production reactors contains moderate amounts of transuranium (TRU) actinides and fission products in addition to the still slightly enriched uranium. Originally, nuclear technology was developed to chemically separate and recover fissionable plutonium from irradiated nuclear fuel for military purposes. Military plutonium separations had essentially ceased by the mid-1990s. Reprocessing, however, can serve multiple purposes, and the relative importance has changed over time. In the 1960’s the vision of the introduction of plutonium-fueled fast-neutron breeder reactors drove the civilian separation of plutonium. More recently, reprocessing has been regarded as a means to facilitate the disposal of high-level nuclear waste, and thus requires development of radically different technical approaches. In the last decade or so, the principal reason for reprocessing has shifted to spent power reactor fuel being reprocessed (1) so that unused uranium and plutonium being recycled reduce the volume, gaining some 25% to 30% more energy from the original uranium in the process and thus contributing to energy security and (2) to reduce the volume and radioactivity of the waste by recovering all long-lived actinides and fission products followed by recycling them in fast reactors where they are transmuted to short-lived fission products; this reduces the volume to about 20%, reduces the long-term radioactivity level in the high-level waste, and complicates the possibility of the plutonium being diverted from civil use – thereby increasing the proliferation resistance of the fuel cycle. In general, reprocessing schemes can be divided into two large categories: aqueous/hydrometallurgical systems, and pyrochemical/pyrometallurgical systems. Worldwide processing schemes are dominated by the aqueous (hydrometallurgical) systems. This document provides a historical review of both categories of reprocessing.

Technical considerations in decisions on plutonium use

International Nuclear Information System (INIS)

Till, C.E.

1980-01-01

Present-day reactors use uranium inefficiently. Really substantial increases in efficiency of uranium utilization require reprocessing. Reprocessing activities give rise to concern about their possible use in fission weapons acquisition. The basic properties of nuclides severely limit both the number of alternative ways that fuel utilization can be improved and the amount of the improvement that is possible from any of the alternatives. By far the greatest improvement comes from plutonium use in a fast reactor. The properties that allow this are peculiar to plutonium. There are basically only two fuel cycles that can be considered as alternatives to the plutonium-238/uranium fuel cycle. One is a uranium-233/thorium fuel cycle, a cycle that is very similar in requirements, including reprocessing, to the plutonium-238/uranium cycle. The other is continuation and refinement of the current once-through cycle. A small number of technical measures to increase proliferation-resistance have been proposed. Improvements of an institutional nature are of two types. The first are improvements in international safeguards - most importantly, nuclear materials accountancy - essentially strengthening or augmenting current IAEA procedures. The second involves agreements between nations to limit distribution of sensitive technologies and to multinationalize or internationalize sensitive elements of the fuel cycle

Research of natural resources saving by design studies of Pressurized Light Water Reactors and High Conversion PWR cores with mixed oxide fuels composed of thorium/uranium/plutonium

International Nuclear Information System (INIS)

Vallet, V.

2012-01-01

Within the framework of innovative neutronic conception of Pressurized Light Water Reactors (PWR) of 3. generation, saving of natural resources is of paramount importance for sustainable nuclear energy production. This study consists in the one hand to design high Conversion Reactors exploiting mixed oxide fuels composed of thorium/uranium/plutonium, and in the other hand, to elaborate multi-recycling strategies of both plutonium and 233 U, in order to maximize natural resources economy. This study has two main objectives: first the design of High Conversion PWR (HCPWR) with mixed oxide fuels composed of thorium/uranium/plutonium, and secondly the setting up of multi-recycling strategies of both plutonium and 233 U, to better natural resources economy. The approach took place in four stages. Two ways of introducing thorium into PWR have been identified: the first is with low moderator to fuel volume ratios (MR) and ThPuO 2 fuel, and the second is with standard or high MR and ThUO 2 fuel. The first way led to the design of under-moderated HCPWR following the criteria of high 233 U production and low plutonium consumption. This second step came up with two specific concepts, from which multi-recycling strategies have been elaborated. The exclusive production and recycling of 233 U inside HCPWR limits the annual economy of natural uranium to approximately 30%. It was brought to light that the strong need in plutonium in the HCPWR dedicated to 233 U production is the limiting factor. That is why it was eventually proposed to study how the production of 233 U within PWR (with standard MR), from 2020. It was shown that the anticipated production of 233 U in dedicated PWR relaxes the constraint on plutonium inventories and favours the transition toward a symbiotic reactor fleet composed of both PWR and HCPWR loaded with thorium fuel. This strategy is more adapted and leads to an annual economy of natural uranium of about 65%. (author) [fr

Experimental studies of U-Pu-Zr fast reactor fuel pins in EBR-II [Experimental Breeder Reactor

International Nuclear Information System (INIS)

Pahl, R.G.; Porter, D.L.; Lahm, C.E.; Hofman, G.L.

1988-01-01

The Integral Fast Reactor (IFR) is a generic reactor concept under development by Argonne National Laboratory. Much of the technology for the IFR is being demonstrated at the Experimental Breeder Reactor II (EBR-II) on the Department of Energy site near Idaho Falls, Idaho. The IFR concept relies on four technical features to achieve breakthroughs in nuclear power economics and safety: (1) a pool-type reactor configuration, (2) liquid sodium cooling, (3) metallic fuel, and (4) an integral fuel cycle with on-site reprocessing. The purpose of this paper will be to summarize our latest results of irradiation testing uranium-plutonium-zirconium (U-Pu-Zr) fuel in the EBR-II. 10 refs., 13 figs., 2 tabs

Simultaneous determination of uranium and plutonium in dissolver solution of irradiated fuel, using ID-TIMS. IRP-11

International Nuclear Information System (INIS)

Shah, Raju; Sasi Bhushan, K.; Govindan, R.; Alamelu, D.; Khodade, P.S.; Aggarwal, S.K.

2007-01-01

A simple sample preparation and simultaneous analysis method to determine uranium and plutonium from dissolver solution, employing the technique of Isotope Dilution Mass spectrometry has been demonstrated. The method used, co-elusion of Uranium and Plutonium from anion exchanger column after initial elution of major part of uranium in 1:5 HNO 3 in order to reduce the initial U/Pu ratio from 1000 to about 100-200 in the co-eluted fraction. Due to the availability of variable multi-collector system, different Faraday cups were adjusted to collect the different ion intensities corresponding to the different masses, during the simultaneous analysis of Uranium and Plutonium, loaded on Re double filament assembly. 233 U and PR grade Plutonium were used as spikes to determine Uranium and Plutonium from dissolver solution of irradiated fuel from research reactor. The possibility of getting the isotopic composition of uranium from the simultaneous analysis of co-eluted purified fraction of U and Pu from spiked aliquots is also explained. (author)

Plutonium Proliferation: The Achilles Heel of Disarmament

International Nuclear Information System (INIS)

Leventhal, Paul

2001-01-01

Plutonium is a byproduct of nuclear fission, and it is produced at the rate of about 70 metric tons a year in the world's nuclear power reactors. Concerns about civilian plutonium ran high in the 1970s and prompted enactment of the Nuclear Non-Proliferation Act of 1978 to give the United States a veto over separating plutonium from U.S.-supplied uranium fuel. Over the years, however, so-called reactor-grade plutonium has become the orphan issue of nuclear non-proliferation, largely as a consequence of pressures from plutonium-separating countries. The demise of the fast breeder reactor and the reluctance of utilities to introduce plutonium fuel in light-water reactors have resulted in large surpluses of civilian, weapons-usable plutonium, which now approach in size the 250 tons of military plutonium in the world. Yet reprocessing of spent fuel for recovery and use of plutonium proceeds apace outside the United States and threatens to overwhelm safeguards and security measures for keeping this material out of the hands of nations and terrorists for weapons. A number of historical and current developments are reviewed to demonstrate that plutonium commerce is undercutting efforts both to stop the spread of nuclear weapons and to work toward eliminating existing nuclear arsenals. These developments include the breakdown of U.S. anti-plutonium policy, the production of nuclear weapons by India with Atoms-for-Peace plutonium, the U.S.-Russian plan to introduce excess military plutonium as fuel in civilian power reactors, the failure to include civilian plutonium and bomb-grade uranium in the proposed Fissile Material Cutoff Treaty, and the perception of emerging proliferation threats as the rationale for development of a ballistic missile defense system. Finally, immobilization of separated plutonium in high-level waste is explored as a proliferation-resistant and disarmament-friendly solution for eliminating excess stocks of civilian and military plutonium.

Lead-cooled fast-neutron reactor (BREST) (Approaches to the closed NFC) - 5435

International Nuclear Information System (INIS)

Dragunov, Y.G.; Lemekhov, V.V.; Moiseyev, A.V.; Smirnov, V.S.; Tocheny, L.V.; Umanskiy, A.A.

2015-01-01

The BREST-OD-300 reactor is under development in Russia. It is an intrinsically safe pilot demonstration lead-cooled fast reactor with uranium-plutonium nitride fuel. This reactor is based on a new concept of inherent safety whose basic principles are: -) the exclusion of severe accidents at the plant (reactivity type, loss of cooling, fires, explosions) that require the resettlement of the population; -) the closing of the nuclear fuel cycle through the burning of minor actinides; -) the environmental acceptability through the maximal reduction of the amount of high-level long-lived radioactive waste nuclides - nuclear fuel cycle products, sent for the final disposal; -) the technological strengthening of non-proliferation. Closed fuel cycle with reactors of BREST type burning minor actinides gives the opportunity to achieve the radiation equivalence between radioactive wastes and natural uranium during a time period about 300 years

Assessment studies on plutonium recycle in CANDU reactors

International Nuclear Information System (INIS)

1978-11-01

This paper describes the CANDU reactor system in detail and goes on to explore the potential for using the system with plutonium recycle fuelling to improve fuel utilisation and to meet the long-term challenge of economic supplies of nuclear fuel. The paper includes comments on costs and non-proliferation aspects. It concludes that: recycle fuelling is feasible with little modification to the reactor design and no degradation of safety, and could offer over 50% savings in uranium requirements. However, recycle fuelling costs do not appear competitive with natural uranium in the CANDU system under current economic conditions

Analysis of refabricated fuel: determination of carbon in uranium plutonium mixed carbide

International Nuclear Information System (INIS)

Huwyler, S.

1977-09-01

In developing uranium plutonium mixed carbide which represents an advanced fuel for breeder reactors carbon analysis is an important means of determining the stoichiometry. Methods of carbon determination are briefly reviewed. The carbon determination using a LECO WR-12 Carbon Determinator is treated in detail and experience of three years operation communicated. Problems arising from operating the LECO-apparatus in a glove box are discussed. It is pointed out that carbon determination with the LECO-apparatus is a very fast method with good precision and well suited for the routine analysis of mixed carbide fuel. The accuracy of the method is checked by means of a standard. (Auth.)

The plutonium recycle for PWR reactors from brazilian nuclear program

International Nuclear Information System (INIS)

Rubini, L.A.

1978-01-01

The purpose of this thesis is to evaluate the material requirements of the nuclear fuel cycle with plutonium recycle. The study starts with the calculation of a reference reactor and has flexibility to evaluate the demand under two alternatives of nuclear fuel cycle for Pressurized Water Reactors (PWR): Without plutonium recycle; and with plutonium recycle. Calculations of the reference reactor have been carried out with the CELL-CORE codes. Variations in the material requirements were studied considering changes in the installed nuclear capacity of PWR reactors, the capacity factor of these reactors, and the introduction of fast breeders. Recycling plutonium produced inside the system can reach economies of about 5% U 3 O 8 and 6% separative work units if recycle is assumed only after the fifth operation cycle of the thermal reactors. (author)

Studies and manufacture of plutonium fuel

International Nuclear Information System (INIS)

Bussy, P.; Mustelier, J.P.; Pascard, R.

1964-01-01

The studies carried out at the C.E.A. on the properties of fast neutron reactor fuels, the manufacture of fuel elements and their behaviour under irradiation are broadly outlined. The metal fuels studied are the ternary alloys U Pu Mo, U Pu Nb, U Pa Ti, U Pa Zr, the ceramic fuels being mixed uranium and plutonium oxides, carbides and nitrides obtained by sintering. Results are given on the manufacture of uranium fuel elements containing a small proportion of plutonium, used in a critical experiment, and on the first experiments in the manufacture of fuel elements for the reactor Rapsodie. Finally the results of irradiation tests carried out on the prototype fuel pins for Rapsodie are described. (authors) [fr

The generation of denatured reactor plutonium by different options of the fuel cycle

Energy Technology Data Exchange (ETDEWEB)

Broeders, C.H.M.; Kessler, G. [Inst. for Neutron Physics and Reactor Technology, Research Center Karlsruhe (Germany)

2006-11-15

Denatured (proliferation resistant) reactor plutonium can be generated in a number of different fuel cycle options. First denatured reactor plutonium can be obtained if, instead of low enriched U-235 PWR fuel, re-enriched U-235/U-236 from reprocessed uranium is used (fuel type A). Also the envisaged existing 2,500 t of reactor plutonium (being generated world wide up to the year 2010), mostly stored in intermediate fuel storage facilities at present, could be converted during a transition phase into denatured reactor plutonium by the options fuel type B and D. Denatured reactor plutonium could have the same safeguards standard as present low enriched (<20% U-235) LWR fuel. It could be incinerated by recycling once or twice in PWRs and subsequently by multi-recycling in FRs (CAPRA type or IFRs). Once denatured, such reactor plutonium could remain denatured during multiple recycling. In a PWR, e.g., denatured reactor plutonium could be destroyed at a rate of about 250 kg/GWey. While denatured reactor plutonium could be recycled and incinerated under relieved IAEA safeguards, neptunium would still have to be monitored by the IAEA in future for all cases in which considerable amounts of neptunium are produced. (orig.)

Final generic environmental statement on the use of recycle plutonium in mixed oxide fuel in light water cooled reactors. Volume 3

International Nuclear Information System (INIS)

1976-08-01

An assessment is presented of the health, safety and environmental effects of the entire light water reactor fuel cycle, considering the comparative effects of three major alternatives: no recycle, recycle of uranium only, and recycle of both uranium and plutonium. The assessment covers the period from 1975 through the year 2000 and includes the cumulative effects for the entire period as well as projections for specific years. Topics discussed include: the light water reactor with plutonium recycle; mixed oxide fuel fabrication; reprocessing plant operations; supporting uranium fuel cycle; transportation of radioactive materials; radioactive waste management; storage of plutonium; radiological health assessment; extended spent fuel storage; and blending of plutonium and uranium at reprocessing plants

Fuel cycle of fast reactor Brest with non-proliferation, transmutation of long-lived nuclides and equivalent disposal of radioactive waste

International Nuclear Information System (INIS)

Lopatkin, A.V.; Orlov, V.V.

2001-01-01

The declared objectives in the fuel cycle of fast reactor BREST achieved by the following measures. Proliferation resistance of the fuel cycle being developed for BREST reactors is provided along two lines: reactors physics and design features; spent fuel reprocessing technology excluding plutonium separation at all process stages. Surplus neutrons produced in a chain reaction in a fast reactor without uranium blanket and the high flux of fast neutrons, allow efficient transmutation of not only all actinides in the core but also long-lived fission products (I, Te) in lead blanket by leakage neutrons without detriment to the inherent safety of this reactor. (author)

Small size modular fast reactors in large scale nuclear power

International Nuclear Information System (INIS)

Zrodnikov, A.V.; Toshinsky, G.I.; Komlev, O.G.; Dragunov, U.G.; Stepanov, V.S.; Klimov, N.N.; Kopytov, I.I.; Krushelnitsky, V.N.

2005-01-01

The report presents an innovative nuclear power technology (NPT) based on usage of modular type fast reactors (FR) (SVBR-75/100) with heavy liquid metal coolant (HLMC) i. e. eutectic lead-bismuth alloy mastered for Russian nuclear submarines' (NS) reactors. Use of this NPT makes it possible to eliminate a conflict between safety and economic requirements peculiar to the traditional reactors. Physical features of FRs, an integral design of the reactor and its small power (100 MWe), as well as natural properties of lead-bismuth coolant assured realization of the inherent safety properties. This made it possible to eliminate a lot of safety systems necessary for the reactor installations (RI) of operating NPPs and to design the modular NPP which technical and economical parameters are competitive not only with those of the NPP based on light water reactors (LWR) but with those of the steam-gas electric power plant. Multipurpose usage of transportable reactor modules SVBR-75/100 of entirely factory manufacture assures their production in large quantities that reduces their fabrication costs. The proposed NPT provides economically expedient change over to the closed nuclear fuel cycle (NFC). When the uranium-plutonium fuel is used, the breeding ratio is over one. Use of proposed NPT makes it possible to considerably increase the investment attractiveness of nuclear power (NP) with fast neutron reactors even today at low costs of natural uranium. (authors)

Uranium/plutonium and uranium/neptunium separation by the Purex process using hydroxyurea

International Nuclear Information System (INIS)

Zhu Zhaowu; He Jianyu; Zhang Zefu; Zhang Yu; Zhu Jianmin; Zhen Weifang

2004-01-01

Hydroxyurea dissolved in nitric acid can strip plutonium and neptunium from tri-butyl phosphate efficiently and has little influence on the uranium distribution between the two phases. Simulating the 1B contactor of the Purex process by hydroxyurea with nitric acid solution as a stripping agent, the separation factors of uranium/plutonium and uranium/neptunium can reach values as high as 4.7 x 10 4 and 260, respectively. This indicates that hydroxyurea is a promising salt free agent for uranium/plutonium and uranium/neptunium separations. (author)

Theoretical methods for determination of core parameters in uranium-plutonium lattices

Energy Technology Data Exchange (ETDEWEB)

Pop-Jordanov, J.; Bosevski, T.; Matausek, M.; Stefanovic, D.; Strugar, P. [Institut za Nuklearne Nauke Boris Kidric, Belgrade (Yugoslavia)

1972-07-01

The prediction of plutonium production in power reactors depends essentially on how the change of neutron energy spectra in a reactor cell during burn-up is determined. In the epithermal region, where the build-up of plutonium occurs, the slowing down effects are particularly important, whereas, on the other hand, the thermal neutron spectrum is strongly influenced by the low-lying plutonium resonances. For accurate analysis, multi-group numerical methods are required, which, applied to burn-up prediction, are extremely laborious and time consuming even for large computers. This paper contains a comprehensive review of the methods of core parameter determination in the uranium-plutonium lattices developed in Yugoslavia during the last few years. Faced with the problem of using small computers, the authors had to find new approaches combining physical evidence and mathematical elegance. The main feature of these approaches is the tendency to proceed with analytical treatment as far as possible and then to include suitable numerical improvements. With this philosophy, which is generally overlooked when using large computers, fast and reasonably accurate methods were developed. The methods include original means for adequate treatment of neutron spectra and cell geometry effects,especially suitable for U-Pu systems. In particular, procedures based on the energy dependent boundary conditions, the discrete energy representation, the improved collision probabilities and the Green function slowing down solutions were developed and applied. Results obtained with these methods are presented and compared with those of the experiments and those obtained with other methods. (author)

Theoretical methods for determination of core parameters in uranium-plutonium lattices

International Nuclear Information System (INIS)

Pop-Jordanov, J.; Bosevski, T.; Matausek, M.; Stefanovic, D.; Strugar, P.

1972-01-01

The prediction of plutonium production in power reactors depends essentially on how the change of neutron energy spectra in a reactor cell during burn-up is determined. In the epithermal region, where the build-up of plutonium occurs, the slowing down effects are particularly important, whereas, on the other hand, the thermal neutron spectrum is strongly influenced by the low-lying plutonium resonances. For accurate analysis, multi-group numerical methods are required, which, applied to burn-up prediction, are extremely laborious and time consuming even for large computers. This paper contains a comprehensive review of the methods of core parameter determination in the uranium-plutonium lattices developed in Yugoslavia during the last few years. Faced with the problem of using small computers, the authors had to find new approaches combining physical evidence and mathematical elegance. The main feature of these approaches is the tendency to proceed with analytical treatment as far as possible and then to include suitable numerical improvements. With this philosophy, which is generally overlooked when using large computers, fast and reasonably accurate methods were developed. The methods include original means for adequate treatment of neutron spectra and cell geometry effects,especially suitable for U-Pu systems. In particular, procedures based on the energy dependent boundary conditions, the discrete energy representation, the improved collision probabilities and the Green function slowing down solutions were developed and applied. Results obtained with these methods are presented and compared with those of the experiments and those obtained with other methods. (author)

A Review of Fast Reactor Programme in India, April 1930

International Nuclear Information System (INIS)

Paranjpe, S.R.

1980-01-01

Nuclear energy has to play a significant role in the energy resources of India in the next century. To-day's apparently vast reserves of fossil fuels would be under severe strain due to rapidly increasing demand for energy. Long-term perspective planning requires Nuclear Energy to play a significant role from early part of the next century and share a major load. But, India is not endowed with vast reserves of uranium and must therefore aim to utilise more abundant thorium reserves which are estimated to be about 350,000 tonnes. Department of Atomic Energy which is responsible for the development of nuclear energy in India has therefore planned a step-wise approach consisting of: (i) First phase of the programme of natural uranium based thermal reactors to produce power and plutonium which is the basis of the next phase. (ii) Second phase of the programme to produce power and breed more and more plutonium through fast breeder deployment so as to build sufficient inventories of fissile material which can then become the basis of the third stage. (iii) To utilise thorium with the help of fissile material produced by 2nd phase of Breeder Reactors

A Review of Fast Reactor Programme in India, April 1930

Energy Technology Data Exchange (ETDEWEB)

Paranjpe, S. R. [Reactor Research Centre Kalpakkam, Tamil Nadu (India)

1980-10-15

Nuclear energy has to play a significant role in the energy resources of India in the next century. To-day's apparently vast reserves of fossil fuels would be under severe strain due to rapidly increasing demand for energy. Long-term perspective planning requires Nuclear Energy to play a significant role from early part of the next century and share a major load. But, India is not endowed with vast reserves of uranium and must therefore aim to utilise more abundant thorium reserves which are estimated to be about 350,000 tonnes. Department of Atomic Energy which is responsible for the development of nuclear energy in India has therefore planned a step-wise approach consisting of: (i) First phase of the programme of natural uranium based thermal reactors to produce power and plutonium which is the basis of the next phase. (ii) Second phase of the programme to produce power and breed more and more plutonium through fast breeder deployment so as to build sufficient inventories of fissile material which can then become the basis of the third stage. (iii) To utilise thorium with the help of fissile material produced by 2nd phase of Breeder Reactors.

Determination of uranium and plutonium by sequential potentiometric titration

International Nuclear Information System (INIS)

Kato, Yoshiharu; Takahashi, Masao

1976-01-01

The determination of uranium and plutonium in mixed oxide fuels has been developed by sequential potentiometric titration. A weighed sample of uranium and plutonium oxides is dissolved in a mixture of nitric and hydrofluoric acids and the solution is fumed with sulfuric acid. After the reduction of uranium and plutonium to uranium(IV) and plutonium(III) by chromium(II) sulfate, 5 ml of buffer solution (KCl-HCl, pH 1.0) is added to the solution. Then the solution is diluted to 30 ml with water and the pH of the solution is adjusted to 1.0 -- 1.5 with 1 M sodium hydroxide. The solution is stirred until the oxidation of the excess of chromium(II) by air is completed. After the removal of dissolved oxygen by bubbling nitrogen through the solution for 10 minutes, uranium (IV) is titrated with 0.1 N cerium(IV) sulfate. Then, plutonium is titrated by 0.02 N cerium(IV) sulfate. When a mixture of uranium and plutonium is titrated with 0.1 N potassium dichromate potentiometrically, the potential change at the end point of plutonium is very small and the end point of uranium is also unclear when 0.1 N potassium permanganate is used as a titrant. In the present method, nitrate, fluoride and copper(II) interfere with the determination of plutonium and uranium. Iron interferes quantitatively with the determination of plutonium but not of uranium. Results obtained in applying the proposed method to 50 mg of mixtures of plutonium and uranium ((7.5 -- 50))% Pu were accurate to within 0.15 mg of each element. (auth.)

Programme of research and development on plutonium recycling in light-water reactors

International Nuclear Information System (INIS)

1979-01-01

This is the third annual progress report concerning the programme on plutonium recycling in light-water reactors (indirect action) of the Commission of the European Communities. It covers the year 1978 and follows the annual reports for 1977 (EUR 6002 EN) and 1976 (EUR 5780). The preliminary results obtained under the 1975-79 programme indicate that: (a) assuming that plutonium recycling in light-water reactors is industrially developed by the end of the century, the foreseeable radiological impact on both workers and the general public can be maintained within the limits of current radiation protection standards; (b) on the whole, there is a good knowledge and mastery of the specific aspects involved in the plutonium recycling in light-water reactors and in particular they indicate that plutonium fuels have a similar behaviour to uranium fuels

The future of plutonium - an overview

International Nuclear Information System (INIS)

Larson, C.E.

1975-01-01

Plutonium is the underpinning of the nuclear industry. Without it it is estimated that the fuel will run out not long after the turn of the century. With plutonium in fast breeders nuclear reactors can be operated for tens of thousands of years and the depleted uranium now available can be utilized The fuel cycle contemplated is similar to that of the light water reactor with some important differences at least partially related to the greater radioactivity of the resulting mixture of plutonium isotopes. The regulatory program does recognize the problems, including those of toxicity, safeguards and transportation. The concept of an integrated fuel cycle facility at a single location must be seriously considered. (author)

Study on hydrogen production using the fast breeder reactors (FBR)

International Nuclear Information System (INIS)

Kani, Yoshio

2003-01-01

As the fast breeder reactor (FBR) can effectively convert uranium-238 difficult to carry out nuclear fission at thermal neutron reactors to nuclear fissionable plutonium-239 to use it remarkable upgrading of application on uranium can be performed, to be expected for sustainable energy source. And, by reuse minor actinides of long half-life nuclides in reprocessed high level wasted solutions for fuels of nuclear reactors, reduction of radioactive poison based on high level radioactive wastes was enabled. As high temperature of about 800 centigrade was required on conventional hydrogen production, by new hydrogen production technique even at operation temperature of sodium-cooled FBR it can be enabled. Here were described for new hydrogen production methods applicable to FBR on palladium membrane hydrogen separation method carrying out natural gas/steam modification at reaction temperature of about 500 centigrade, low temperature thermo-chemical method expectable simultaneous simplification of production process, and electrolysis method expected on power load balancing. (G.K.)

Advanced fuels for plutonium management in pressurized water reactors

International Nuclear Information System (INIS)

Vasile, A.; Dufour, Ph.; Golfier, H.; Grouiller, J.P.; Guillet, J.L.; Poinot, Ch.; Youinou, G.; Zaetta, A.

2003-01-01

Several fuel concepts are under investigation at CEA with the aim of manage plutonium inventories in pressurized water reactors. This options range from the use of mature technologies like MOX adapted in the case of MOX-EUS (enriched uranium support) and COmbustible Recyclage A ILot (CORAIL) assemblies to more innovative technologies using IMF like DUPLEX and advanced plutonium assembly (APA). The plutonium burning performances reported to the electrical production go from 7 to 60 kg (TW h) -1 . More detailed analysis covering economic, sustainability, reliability and safety aspects and their integration in the whole fuel cycle would allow identifying the best candidate

Oxygen potential of uranium--plutonium oxide as determined by controlled-atmosphere thermogravimetry

International Nuclear Information System (INIS)

Swanson, G.C.

1975-10-01

The oxygen-to-metal atom ratio, or O/M, of solid solution uranium-plutonium oxide reactor fuel is a measure of the concentration of crystal defects in the oxide which affect many fuel properties, particularly, fuel oxygen potential. Fabrication of a high-temperature oxygen electrode, employing an electro-active tip of oxygen-deficient solid-state electrolyte, intended to confirm gaseous oxygen potentials is described. Uranium oxide and plutonium oxide O/M reference materials were prepared by in situ oxidation of high purity metals in the thermobalance. A solid solution uranium-plutonium oxide O/M reference material was prepared by alloying the uranium and plutonium metals in a yttrium oxide crucible at 1200 0 C and oxidizing with moist He at 250 0 C. The individual and solid solution oxides were isothermally equilibrated with controlled oxygen potentials between 800 and 1300 0 C and the equilibrated O/M ratios calculated with corrections for impurities and buoyancy effects. Use of a reference oxygen potential of -100 kcal/mol to produce an O/M of 2.000 is confirmed by these results. However, because of the lengthy equilibration times required for all oxides, use of the O/M reference materials rather than a reference oxygen potential is recommended for O/M analysis methods calibrations. (auth)

Status of sodium cooled fast reactors with closed fuel cycle in India

International Nuclear Information System (INIS)

Raj, B.

2007-01-01

Fast reactors form the second stage of India's 3-stage nuclear power programme. The seed for India's fast reactor programme was sown through the construction of the Fast Breeder Test Reactor (FBTR) at IGCAR, Kalpakkam, that was commissioned in 1985. FBTR has operated with an unique, indigenously developed plutonium rich mixed carbide fuel, which has reached a burn up as high as 155 GWd/t without any fuel failure in the core. The sodium systems in the reactor have performed excellently. The availability of the reactor has been as high as 92% in the recent campaigns. The fuel discharged from FBTR up to 100 GWd/t has been reprocessed successfully. The experience gained in the construction, commissioning and operation of FBTR has provided the necessary confidence to launch a Prototype FBR of 500 MWe capacity (PFBR). This reactor will be fuelled by uranium, plutonium mixed oxide. The reactor construction started in 2003 and the reactor is scheduled to be commissioned by 2010. The design of the reactor has incorporated the worldwide operating experience from the FBRs and has addressed various safety issues reported in literature, besides introducing a number of innovative features which have reduced the unit energy cost and contributed to its enhanced safety. Simultaneous with the construction of the reactor, the fuel cycle of the reactor has been addressed in a comprehensive manner and construction of a fuel cycle facility has been initiated. Subsequent to the PFBR, 4 more reactors with identical design are proposed to be constructed. Various elements of reactor design are being carefully analysed with the aim of introducing innovative features towards further reduction in unit energy cost and enhancing safety in these reactors

Characterization of past and present solid waste streams from the Plutonium-Uranium Extraction Plant

International Nuclear Information System (INIS)

Pottmeyer, J.A.; Weyns, M.I.; Lorenzo, D.S.; Vejvoda, E.J.; Duncan, D.R.

1993-04-01

During the next two decades the transuranic wastes, now stored in the burial trenches and storage facilities at the Hanford Site, are to be retrieved, processed at the Waste Receiving and Processing Facility, and shipped to the Waste Isolation Pilot Plant near Carlsbad, New Mexico for final disposal. Over 7% of the transuranic waste to be retrieved for shipment to the Waste Isolation Pilot Plant has been generated at the Plutonium-Uranium Extraction (PUREX) Plant. The purpose of this report is to characterize the radioactive solid wastes generated by PUREX using process knowledge, existing records, and oral history interviews. The PUREX Plant is currently operated by the Westinghouse Hanford Company for the US Department of Energy and is now in standby status while being prepared for permanent shutdown. The PUREX Plant is a collection of facilities that has been used primarily to separate plutonium for nuclear weapons from spent fuel that had been irradiated in the Hanford Site's defense reactors. Originally designed to reprocess aluminum-clad uranium fuel, the plant was modified to reprocess zirconium alloy clad fuel elements from the Hanford Site's N Reactor. PUREX has provided plutonium for research reactor development, safety programs, and defense. In addition, the PUREX was used to recover slightly enriched uranium for recycling into fuel for use in reactors that generate electricity and plutonium. Section 2.0 provides further details of the PUREX's physical plant and its operations. The PUREX Plant functions that generate solid waste are as follows: processing operations, laboratory analyses and supporting activities. The types and estimated quantities of waste resulting from these activities are discussed in detail

Plutonium and U-233 mines

International Nuclear Information System (INIS)

Milgram, M.S.

1983-08-01

A comparison is made among second generation reactor systems fuelled primarily with fissile plutonium and/or U-233 in uranium or thorium. This material is obtained from irradiated fuel from first generation CANDU reactors fuelled by natural or enriched uranium and thorium. Except for plutonium-thorium reactors, second generation reactors demand similar amounts of reprocessing throughput, but the most efficient plutonium burning systems require a large prior allocation of uranium. Second generation reactors fuelled by U-233 make more efficient use of resources and lead to more flexible fuelling strategies, but require development of first generation once-through thorium cycles and early demonstration of the commercial viability of thorium fuel reprocessing. No early implementation of reprocessing technology is required for these cycles

SEPARATION OF URANIUM, PLUTONIUM, AND FISSION PRODUCTS

Science.gov (United States)

Spence, R.; Lister, M.W.

1958-12-16

Uranium and plutonium can be separated from neutron-lrradiated uranium by a process consisting of dissolvlng the lrradiated material in nitric acid, saturating the solution with a nitrate salt such as ammonium nitrate, rendering the solution substantially neutral with a base such as ammonia, adding a reducing agent such as hydroxylamine to change plutonium to the trivalent state, treating the solution with a substantially water immiscible organic solvent such as dibutoxy diethylether to selectively extract the uranium, maklng the residual aqueous solutlon acid with nitric acid, adding an oxidizing agent such as ammonlum bromate to oxidize the plutonium to the hexavalent state, and selectlvely extracting the plutonium by means of an immlscible solvent, such as dibutoxy dlethyletber.

Decommissioning the Los Alamos Molten Plutonium Reactor Experiment (LAMPRE I)

International Nuclear Information System (INIS)

Harper, J.R.; Garde, R.

1981-11-01

The Los Alamos Molten Plutonium Reactor Experiment (LAMPRE I) was decommissioned at the Los Alamos National Laboratory, Los Alamos, New Mexico, in 1980. The LAMPRE I was a sodium-cooled reactor built to develop plutonium fuels for fast breeder applications. It was retired in the mid-1960s. This report describes the decommissioning procedures, the health physics programs, the waste management, and the costs for the operation

The relationship between natural uranium and advanced fuel cycles in CANDU reactors

International Nuclear Information System (INIS)

Lane, A.D.; McDonnell, F.N.; Griffiths, J.

1988-11-01

CANDU is the most uranium-economic type of thermal power reactor, and is the only type used in Canada. CANDU reactors consume approximately 15% of Canadian uranium production and support a fuel service industry valued at ∼$250 M/a. In addition to their once-through, natural-uranium fuel cycle, CANDU reactors are capable of operating with slightly-enriched uranium (SEU), uranium-plutonium and thorium cycles, more efficiently than other reactors. Only SEU is economically attractive in Canada now, but the other cycles are of interest to countries without indigenous fuel resources. A program is underway to establish the fuel technologies necessary for the use of SEU and the other fuel cycles in CANDU reactors. 22 refs

Plutonium burning and minor actinides transmutation in fast reactors: first results obtained within the frame of the CAPRA programme

International Nuclear Information System (INIS)

Garnier, J.C.; Rouault, J.; Kiefhaber, E.; Sunderland, R.

1994-01-01

The CAPRA program gas been established by the CEA in early 1993 with the primary goal of investigating the feasibility of a fast reactor core optimised to burn plutonium. CAPRA is now being jointly pursued by the European Research and Development (R and D) organisations (CEA in France, AEA in the UK and KFK in Germany) and the design companies grouped under the European Fast Reactor Associates umbrella. The first phase of the CAPRA programme is planned to last until the end of 1994. Its goal is to deliver an overall assessment on the feasibility of fast reactor plutonium burner cores. This assessment will also include the minor actinides transmutation capability of such cores. The objective of this paper is to present the progress made so far. After an introduction to the basic physics boundary conditions of burner cores, a description of the studies performed and the main results are given. Then the efforts made towards the definition of an accompanying experimental Research and Development (R and D) program are summarised, followed by the conclusions and an outlook to the future work. (authors). 4 refs., 3 figs., 2 tabs

EDF research scenarios for closing the Plutonium cycle

International Nuclear Information System (INIS)

Le Mer, Joël; Garzenne, Claude; Lemasson, David

2013-01-01

Conclusion: → There are various solutions to plutonium fuel closure; → Natural uranium consumption is reduced: • Full generation IV fleet is obviously the most efficient; • Symbiotic fleet makes a better use of its advanced reactors. → Plutonium inventory reaches an equilibrium between 700 tons and 1150 tons. • The multi-recycling of spent MOX fuel must be a long term solution in order to reduce significantly the plutonium inventory. → Spent fuel storage is reduced when MOX spent fuel are reprocessed but sodium pools are challenging. → Fast reactors are not the only solution to use MOX spent fuel: • HCPWR is a roundabout solution: – the reduction of natural uranium is limited; – the high level waste production is high. – The reprocessing plant capacity must be increased during deployment phase → R&D must be continued to improve HCPWR design

Criticality of mixtures of plutonium and high enriched uranium

International Nuclear Information System (INIS)

Grolleau, E.; Lein, M.; Leka, G.; Maidou, B.; Klenov, P.

2003-01-01

This paper presents a criticality evaluation of moderated homogeneous plutonium-uranium mixtures. The fissile media studied are homogeneous mixtures of plutonium and high enriched uranium in two chemical forms: aqueous mixtures of metal and mixtures of nitrate solutions. The enrichment of uranium considered are 93.2wt.% 235 U and 100wt.% 235 U. The 240 Pu content in plutonium varies from 0wt.% 240 Pu to 12wt.% 240 Pu. The critical parameters (radii and masses of a 20 cm water reflected sphere) are calculated with the French criticality safety package CRISTAL V0. The comparison of the calculated critical parameters as a function of the moderator-to-fuel atomic ratio shows significant ranges in which high enriched uranium systems, as well as plutonium-uranium mixtures, are more reactive than plutonium systems. (author)

Burning weapons-grade plutonium in reactors

International Nuclear Information System (INIS)

Newman, D.F.

1993-06-01

As a result of massive reductions in deployed nuclear warheads, and their subsequent dismantlement, large quantities of surplus weapons- grade plutonium will be stored until its ultimate disposition is achieved in both the US and Russia. Ultimate disposition has the following minimum requirements: (1) preclude return of plutonium to the US and Russian stockpiles, (2) prevent environmental damage by precluding release of plutonium contamination, and (3) prevent proliferation by precluding plutonium diversion to sub-national groups or nonweapons states. The most efficient and effective way to dispose of surplus weapons-grade plutonium is to fabricate it into fuel and use it for generation of electrical energy in commercial nuclear power plants. Weapons-grade plutonium can be used as fuel in existing commercial nuclear power plants, such as those in the US and Russia. This recovers energy and economic value from weapons-grade plutonium, which otherwise represents a large cost liability to maintain in safeguarded and secure storage. The plutonium remaining in spent MOX fuel is reactor-grade, essentially the same as that being discharged in spent UO 2 fuels. MOX fuels are well developed and are currently used in a number of LWRs in Europe. Plutonium-bearing fuels without uranium (non-fertile fuels) would require some development. However, such non-fertile fuels are attractive from a nonproliferation perspective because they avoid the insitu production of additional plutonium and enhance the annihilation of the plutonium inventory on a once-through fuel cycle

Actinide recycle potential in the Integral Fast Reactor (IFR) fuel cycle

International Nuclear Information System (INIS)

Chang, Y.I.; Till, C.E.

1990-01-01

In the Integral Fast Reactor (IFR) development program, the entire reactor system -- reactor, fuel cycle, and waste process is being developed and optimized at the same time as a single integral entity. The use of metallic fuel in the IFR allows a radically improved fuel cycle technology. Pyroprocessing, which utilizes high temperatures and molten salt and molten metal solvents, can be advantageously utilized for processing metal fuels because the product is metal suitable for fabrication into new fuel elements. The key step in the IFR process is electrorefining, which provides for recovery of the valuable fuel constituents, uranium and plutonium, and for removal of fission products. In the electrorefining operation, uranium and plutonium are selectively transported from an anode to a cathode, leaving impurity elements, mainly fission products, either in the anode compartment or in a molten salt electrolyte. A notable feature of the IFR process is that the actinide elements accompany plutonium through the process. This results in a major advantage in the high-level waste management, because these actinides are automatically recycled back into the reactor for in-situ burning. Based on the recent IFR process development, a preliminary assessment has also been made to investigate the feasibility of further adapting the pyrochemical processes to directly extract actinides from LWR spent fuel. The results of this assessment indicate very promising potential and two most promising flowsheet options have been identified for further research and development. This paper also summarizes current thinking on the rationale for actinide recycle, its ramifications on the geologic repository and the current high-level waste management plans, and the necessary development programs. 5 refs., 4 figs., 4 tabs

The use of plutonium

International Nuclear Information System (INIS)

Marshall, W.

1980-01-01

The use of plutonium as a vital energy source producing maximum economic benefit with minimum proliferation risks is discussed. Having considered the production of plutonium, several possible plutonium fuel cycle options are identified and the economic value to be attached to plutonium for each examined. It is shown how the use of plutonium in fast reactors gives an opportunity for a non-proliferation policy not available when plutonium is used only in thermal reactors. From the technical considerations reviewed concerning plutonium and fast reactors it is shown that an economic regime involving international trade in spent thermal reactor fuel is possible which benefits equally those countries with fast reactors and those without and also assists in avoiding the proliferation of nuclear weapons. (U.K.)

Plutonium use - Present status and prospects

International Nuclear Information System (INIS)

Dievoet, J. van; Fossoul, E.; Jonckheere, E.; Bemden, E. van den

1977-01-01

The use of plutonium in thermal and fast reactors is a demonstrated, if not proven, technology. Moreover, plutonium is being produced in increasing quantities. Evaluation of this production on a world scale shows that it would be theoretically possible to construct numerous breeders and thus to make the best use of plutonium, while considerably reducing uranium consumption. This source of plutonium is nevertheless dependent on the reprocessing of irradiated fuel. Long delays in installing and adequate world reprocessing capacity are weakening the prospects for introducing breeders. Furthermore, the critical situation regarding reprocessing may delay the development of complementary reprocessing methods for fuels with a high plutonium content and high burnup. The recycling of plutonium is now a well-known technique and any objections to it hardly bear analysis. Utilization of plutonium offers an appreciable saving in terms of uranium and separative work units; and it can also be shown that immediate reprocessing of the recycling fuel is not essential for the economics of the concept. Temporary storage of recycled fuel is a particularly safe form of concentrating plutonium, namely in irradiated plutonium-bearing fuel assemblies. Finally, recycling offers such flexibility that it represents no obstacle to fuel management at power plants with light-water reactors. These strategic considerations imply that the technology of using plutonium for fabricating thermal or fast reactor fuels is both technically reliable and economically viable. The methods used in industrial facilities are fully reassuring in this respect. Although various unsolved problems exist, none seems likely to impede current developments, while the industrial experience gained has enabled the economics and reliability of the methods to be improved appreciably. Apart from the techno-economic aspects, the plutonium industry must face extremely important problems in connection with the safety of personnel

Behavior of actinides in the Integral Fast Reactor fuel cycle

Energy Technology Data Exchange (ETDEWEB)

Courtney, J.C. [Louisiana State Univ., Baton Rouge, LA (United States). Nuclear Science Center; Lineberry, M.J. [Argonne National Lab., Idaho Falls, ID (United States). Technology Development Div.

1994-06-01

The Integral Fast Reactor (IFR) under development by Argonne National Laboratory uses metallic fuels instead of ceramics. This allows electrorefining of spent fuels and presents opportunities for recycling minor actinide elements. Four minor actinides ({sup 237}Np, {sup 240}Pu, {sup 241}Am, and {sup 243}Am) determine the waste storage requirements of spent fuel from all types of fission reactors. These nuclides behave the same as uranium and other plutonium isotopes in electrorefining, so they can be recycled back to the reactor without elaborate chemical processing. An experiment has been designed to demonstrate the effectiveness of the high-energy neutron spectra of the IFR in consuming these four nuclides and plutonium. Eighteen sets of seven actinide and five light metal targets have been selected for ten day exposure in the Experimental Breeder Reactor-2 which serves as a prototype of the IFR. Post-irradiation analyses of the exposed targets by gamma, alpha, and mass spectroscopy are used to determine nuclear reaction-rates and neutron spectra. These experimental data increase the authors` confidence in their ability to predict reaction rates in candidate IFR designs using a variety of neutron transport and diffusion programs.

Actinide behavior in the Integral Fast Reactor. Final project report

Energy Technology Data Exchange (ETDEWEB)

Courtney, J.C.

1994-11-01

The Integral Fast Reactor (IFR) under development by Argonne National Laboratory uses metallic fuels instead of ceramics. This allows electrorefining of spent fuels and presents opportunities for recycling minor actinide elements. Four minor actinides ({sup 237}Np, {sup 240}Pu, {sup 241}Am, and {sup 243}Am) determine the waste storage requirements of spent fuel from all types of fission reactors. These nuclides behave the same as uranium and other plutonium isotopes in electrorefining, so they can be recycled back to the reactor without elaborate chemical processing. An experiment has been designed to demonstrate the effectiveness of the high-energy neutron spectra of the IFR in consuming these four nuclides and weapons grade plutonium. Eighteen sets of seven actinide and five light metal targets have been selected for seven day exposure in the Experimental Breeder Reactor-II which serves as a prototype of the IFR. Post-irradiation analyses of the exposed targets by gamma, alpha, and mass spectroscopy are used to determine nuclear reaction rates and neutron spectra. These experimental data increase the authors confidence in their ability to predict reaction rates in candidate IFR designs using a variety of neutron transport and diffusion programs.

Actinide behavior in the Integral Fast Reactor. Final project report

International Nuclear Information System (INIS)

Courtney, J.C.

1994-11-01

The Integral Fast Reactor (IFR) under development by Argonne National Laboratory uses metallic fuels instead of ceramics. This allows electrorefining of spent fuels and presents opportunities for recycling minor actinide elements. Four minor actinides ( 237 Np, 240 Pu, 241 Am, and 243 Am) determine the waste storage requirements of spent fuel from all types of fission reactors. These nuclides behave the same as uranium and other plutonium isotopes in electrorefining, so they can be recycled back to the reactor without elaborate chemical processing. An experiment has been designed to demonstrate the effectiveness of the high-energy neutron spectra of the IFR in consuming these four nuclides and weapons grade plutonium. Eighteen sets of seven actinide and five light metal targets have been selected for seven day exposure in the Experimental Breeder Reactor-II which serves as a prototype of the IFR. Post-irradiation analyses of the exposed targets by gamma, alpha, and mass spectroscopy are used to determine nuclear reaction rates and neutron spectra. These experimental data increase the authors confidence in their ability to predict reaction rates in candidate IFR designs using a variety of neutron transport and diffusion programs

Behavior of actinides in the Integral Fast Reactor fuel cycle

International Nuclear Information System (INIS)

Courtney, J.C.; Lineberry, M.J.

1994-01-01

The Integral Fast Reactor (IFR) under development by Argonne National Laboratory uses metallic fuels instead of ceramics. This allows electrorefining of spent fuels and presents opportunities for recycling minor actinide elements. Four minor actinides ( 237 Np, 240 Pu, 241 Am, and 243 Am) determine the waste storage requirements of spent fuel from all types of fission reactors. These nuclides behave the same as uranium and other plutonium isotopes in electrorefining, so they can be recycled back to the reactor without elaborate chemical processing. An experiment has been designed to demonstrate the effectiveness of the high-energy neutron spectra of the IFR in consuming these four nuclides and plutonium. Eighteen sets of seven actinide and five light metal targets have been selected for ten day exposure in the Experimental Breeder Reactor-2 which serves as a prototype of the IFR. Post-irradiation analyses of the exposed targets by gamma, alpha, and mass spectroscopy are used to determine nuclear reaction-rates and neutron spectra. These experimental data increase the authors' confidence in their ability to predict reaction rates in candidate IFR designs using a variety of neutron transport and diffusion programs

Accountability methods for plutonium and uranium: the NRC manuals

Energy Technology Data Exchange (ETDEWEB)

Gutmacher, R.G.; Stephens, F.B.

1977-09-28

Four manuals containing methods for the accountability of plutonium nitrate solutions, plutonium dioxide, uranium dioxide and mixed uranium-plutonium oxide have been prepared by us and issued by the U.S. Nuclear Regulatory Commission. A similar manual on methods for the accountability of uranium and plutonium in reprocessing plant dissolver solutions is now in preparation. In the present paper, we discuss the contents of the previously issued manuals and give a preview of the manual now being prepared.

Accountability methods for plutonium and uranium: the NRC manuals

International Nuclear Information System (INIS)

Gutmacher, R.G.; Stephens, F.B.

1977-01-01

Four manuals containing methods for the accountability of plutonium nitrate solutions, plutonium dioxide, uranium dioxide and mixed uranium-plutonium oxide have been prepared by us and issued by the U.S. Nuclear Regulatory Commission. A similar manual on methods for the accountability of uranium and plutonium in reprocessing plant dissolver solutions is now in preparation. In the present paper, we discuss the contents of the previously issued manuals and give a preview of the manual now being prepared

Future fuel cycle development for CANDU reactors

International Nuclear Information System (INIS)

Hatcher, S.R.; McDonnell, F.N.; Griffiths, J.; Boczar, P.G.

1987-01-01

The CANDU reactor has proven to be safe and economical and has demonstrated outstanding performance with natural uranium fuel. The use of on-power fuelling, coupled with excellent neutron economy, leads to a very flexible reactor system with can utilize a wide variety of fuels. The spectrum of fuel cycles ranges from natural uranium, through slightly enriched uranium, to plutonium and ultimately thorium fuels which offer many of the advantages of the fast breeder reactor system. CANDU can also burn the recycled uranium and/or the plutonium from fuel discharged from light water reactors. This synergistic relationship could obviate the need to re-enrich the reprocessed uranium and allow a simpler reprocessing scheme. Fule management strategies that will permit future fuel cycles to be used in existing CANDU reactors have been identified. Evolutionary design changes will lead to an even greater flexibility, which will guarantee the continued success of the CANDU system. (author)

Economic considerations of plutonium utilization in the nuclear power strategy of Finland

International Nuclear Information System (INIS)

Silvennoinen, P.; Tusa, E.; Routti, J.T.

1977-01-01

Based on the current and predicted share of nuclear power in the national energy supply strategy, an optimal programme is developed for the exploitation of plutonium in both light-water and fast reactor systems. Assuming cost trends beyond the year 2000 for uranium, plutonium, uranium enrichment, fuel fabrication and assessing the availability of plutonium from domestic power plants and from abroad, the nuclear construction programme is optimized economically in view of the estimated development in the investment costs of various plant types. Given the expected nuclear share of the energy procurement this sector is covered by the alternative production schemes, i.e. light-water reactors with and without plutonium recycle, and fast reactors. Defining the objective function in terms of minimized revenue requirement in plant amortization and operation the generated scenarios are screened off and they finally converge to the optimal policy of nuclear power construction up to the year 2000. The established technology is associated with a larger share of the domestic manufacturing and the introduction of a new fuel or reactor type is taken to correspond to a reduced domestic investment share. In the investment costs the domestic fraction is regarded competitive up to a certain marginal excess. Plutonium recycle is seen to be competitive from 1985 or as soon as the required amount of fuel has been reprocessed. The domestic accumulation of plutonium will be able to support the introduction of the LMFBR in 1997. Owing to the uncertainties prevailing in the forecasts, sensitivity studies are performed as functions of the major economic parameters and their temporal development. (author)

Fabrication and Pre-irradiation Characterization of a Minor Actinide and Rare Earth Containing Fast Reactor Fuel Experiment for Irradiation in the Advanced Test Reactor

Energy Technology Data Exchange (ETDEWEB)

Timothy A. Hyde

2012-06-01

The United States Department of Energy, seeks to develop and demonstrate the technologies needed to transmute the long-lived transuranic actinide isotopes contained in spent nuclear fuel into shorter lived fission products, thereby decreasing the volume of material requiring disposal and reducing the long-term radiotoxicity and heat load of high-level waste sent to a geologic repository. This transmutation of the long lived actinides plutonium, neptunium, americium and curium can be accomplished by first separating them from spent Light Water Reactor fuel using a pyro-metalurgical process, then reprocessing them into new fuel with fresh uranium additions, and then transmuted to short lived nuclides in a liquid metal cooled fast reactor. An important component of the technology is developing actinide-bearing fuel forms containing plutonium, neptunium, americium and curium isotopes that meet the stringent requirements of reactor fuels and materials.

Metallic uranium as fuel for fast reactors

International Nuclear Information System (INIS)

Moura Neto, C. de

1988-01-01

This paper presents a first overview of the use of metallic uranium and its alloys as an option for fuel for rapid reactors. Aspects are discussed concerning uranium alloys which present high solubility in the gamma phase. (author)

Investigation of environmental samples from Fukushima with respect to uranium and plutonium by AMS; Untersuchung von Umweltproben aus Fukushima in Bezug auf Plutonium und Uran mittels AMS

Energy Technology Data Exchange (ETDEWEB)

Schneider, Stephanie

2017-02-01

In March 2011, the nuclear power plant Fukushima Dai-ichi was seriously damaged by a tsunami caused by an earthquake. During the accident large quantities of radionuclides, mainly of the volatile elements cesium and iodine, were released to the environment. In small amounts refractory elements such as plutonium and uranium have also been released. Plutonium and the uraniumisotope {sup 236}U have primarily been delivered by human activities in the environment. Large amounts were released during the atmospheric nuclear weapons tests. Additional sources are accidents in nuclear facilities, like Chernobyl. Every source has its own characteristic isotopic composition. It is therefore possible to determine the origin of the contamination by measuring the isotopic ratios of {sup 240}Pu/{sup 239}Pu and {sup 236}U/{sup 238}U. These ratios can be determined by using accelerator mass spectrometry. Due to its high sensitivity, it is possible to measure even small amounts of plutonium and especially of {sup 236}U. These measurements were performed using the compact 500 kV facility ''TANDY'' of ETH Zurich. In 2013 and 2015 vegetation, litter and soil drill core samples were taken in the contaminated area in Fukushima prefecture. In 2015 samples were taken as close to the sampling locations of the 2013 campaign as possible. After isolation of plutonium and uranium by chemical extraction, separate targets were prepared for the measurement. The {sup 240}Pu/{sup 239}Pu ratios indicate global fallout as the plutonium source for most samples. The plutonium of the reactors of Fukushima Dai-ichi is located in the upper layers like in vegetation or litter. From the uranium ratios alone the reactors could not unambigously be identified as the source of {sup 236}U. However, this is plausible in the cases were reactor plutonium was detected. None of the samples contained higher plutonium activity concentrations than in the rest of Japan, caused by global fallout. This

Construction of fast experimental reactor 'Joyo' from start of construction to criticality

International Nuclear Information System (INIS)

Sakata, Hajime

1977-01-01

The fast experimental reactor ''Joyo'' is a sodium-cooled, fast neutron reactor using mixed oxide of uranium and plutonium, the first in Japan. The purposes of its construction are to experience and solve the various technical problems expected in the constructions of the prototype reactor ''Monju'' and future practical reactors, and to use as the irradiation facility for developing the fuel and material for fast breeder reactors in Japan after the completion. The construction finished by the end of 1974, and the synthetic functional test was carried out for about two years thereafter. The whole installation was handed over to PNC on March 8, 1977. The reactor attained the criticality on April 24, 1977. The outline of the construction works is described. ''Guidance to the structural design of sodium machinery for Joyo'' was compiled, and the analysis was made according to it. Moreover, various inspection standards regarding welding, electrical machinery, fuel and others were made. The revision of the design for improving the safety and performance was made during the construction at all times. The synthetic functional test was carried out for about two years on 266 items, and subsequently, the criticality test was completed satisfactorily. (Kako, I.)

Long-term scenarios of power reactors and fuel cycle development and the role of reduced moderation water reactors

International Nuclear Information System (INIS)

Sato, Osamu; Tatematsu, Kenji; Tanaka, Yoji

2000-01-01

Reduced moderation spectrum reactor is one of water cooled type reactors in future, which is based on the advanced technology of conventional nuclear power plants. The reduced moderation water reactor (RMWR) has various advantages, such as effective utilization of uranium resources, high conversion ratio, high burn-up, long-term cycle operation, and multiple recycle of plutonium. The RMWR is expected to be a substitute of fast breeder reactor (FBR) of which the development encounters with some technical and financial difficulties, and discontinues in many countries. The role of the RMWR on long-term scenarios of power reactor and fuel cycle development in Japan is investigated from the point of view of uranium resource needed. The consumption of natural uranium needed up to the year 2200 is calculated on various assumptions for the following three cases: (1) no breeder reactor; plutonium-thermal cycle in conventional light water reactor, (2) introduction of the FBR, and (3) introduction of the RMWR. The amounts of natural uranium consumption depends largely on the conversion ratio and plutonium quantity needed of a reactor type. The RMWR has a possibility as a substitute technology of the FBR with the improvement of conversion ratio and high burn-up. (Suetake, M.)

Long-term scenarios of power reactors and fuel cycle development and the role of reduced moderation water reactors

Energy Technology Data Exchange (ETDEWEB)

Sato, Osamu; Tatematsu, Kenji; Tanaka, Yoji [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

2000-06-01

Reduced moderation spectrum reactor is one of water cooled type reactors in future, which is based on the advanced technology of conventional nuclear power plants. The reduced moderation water reactor (RMWR) has various advantages, such as effective utilization of uranium resources, high conversion ratio, high burn-up, long-term cycle operation, and multiple recycle of plutonium. The RMWR is expected to be a substitute of fast breeder reactor (FBR) of which the development encounters with some technical and financial difficulties, and discontinues in many countries. The role of the RMWR on long-term scenarios of power reactor and fuel cycle development in Japan is investigated from the point of view of uranium resource needed. The consumption of natural uranium needed up to the year 2200 is calculated on various assumptions for the following three cases: (1) no breeder reactor; plutonium-thermal cycle in conventional light water reactor, (2) introduction of the FBR, and (3) introduction of the RMWR. The amounts of natural uranium consumption depends largely on the conversion ratio and plutonium quantity needed of a reactor type. The RMWR has a possibility as a substitute technology of the FBR with the improvement of conversion ratio and high burn-up. (Suetake, M.)

Importance of resonance parameters of fertile nuclei and of 239Pu isotope for fast power reactors

International Nuclear Information System (INIS)

Barre, J.Y.; Khairallah, A.

1975-01-01

The importance of resonance parameters of fertile nuclei and of 239 Pu isotope for fast power reactors will be restricted, in this presentation, to mixed oxide-uranium-plutonium fuelled sodium-cooled and uranium-oxide-sodium reflected fast reactors. The power range lies between 200 and 2000 MWe. Among the topics of this specialist meeting, the isotopes to be considered are, primarly 239 Pu then 238 U and 240 Pu. Resonance parameters are mainly used in fast power reactor calculations through the well-known concept of self shielding factors. After a short description of the determination and the use of these self-shielding factors, their sensitivities to resonance parameters are characterized from some specific examples: those sensitivities are small. Then, the main design parameters sensitive to the amplitude of self-shielding factors are considered: critical enrichment, global breeding gain. The relative importance of isotope, reaction rate and energy range are mentionned. In a third part, the Doppler effect, sensitive to the temperature variation of self-shielding factors, is considered in the same way. Finally, it is concluded that the present knowledge of resonance parameters for 238 U, 239 Pu and 240 Pu is sufficient for fast power reactors from a designer point of view [fr

The use of the average plutonium-content for criticality evaluation of boiling water reactor mixed oxide-fuel transport and storage packages

International Nuclear Information System (INIS)

Mattera, C.

2003-01-01

Currently in France, criticality studies in transport configurations for Boiling Water Reactor Mixed Oxide fuel assemblies are based on conservative hypothesis assuming that all rods (Mixed Oxide (Uranium and Plutonium), Uranium Oxide, Uranium and (Gadolinium Oxide rods) are Mixed Oxide rods with the same Plutonium-content, corresponding to the maximum value. In that way, the real heterogeneous mapping of the assembly is masked and covered by an homogenous Plutonium-content assembly, enriched at the maximum value. As this calculation hypothesis is extremely conservative, Cogema Logistics (formerly Transnucleaire) has studied a new calculation method based on the use of the average Plutonium-content in the criticality studies. The use of the average Plutonium-content instead of the real Plutonium-content profiles provides a highest reactivity value that makes it globally conservative. This method can be applied for all Boiling Water Reactor Mixed Oxide complete fuel assemblies of type 8 x 8, 9 x 9 and 10 x 10 which Plutonium-content in mass weight does not exceed 15%; it provides advantages which are discussed in the paper. (author)

A contribution to the study of the mixed uranium-plutonium mono-carbides containing small quantities of zirconium

International Nuclear Information System (INIS)

Bocker, S.

1970-03-01

We have studied a mixed monocarbide, type (U,Pu)C, containing small additions of zirconium for the application as a fast neutron reactor fuel. A preliminary study was conducted on the (U,Zr)C monocarbide (Report CEA-R-3765(1). It was found that small additions of zirconium to the uranium-plutonium monocarbide improve a number of properties such as atmospheric corrosion, the hardness, and particularly the compatibility with 316 stainless steel. However, properties such as the coefficient of expansion and the melting point are only slightly changed. The relative percentage of Pu/U+Pu in the monocarbide was fixed at 20 per cent. Two processes of fabrication were employed: casting in an arc furnace, sintering, carried out after having the hydrides of the metals carburized. The metallurgical results indicate, that the above mentioned fuel might be of interest for fast neutron reactor application. (author) [fr

Environmental sensitivity studies for Gen-IV roadmap fast reactor scenario

International Nuclear Information System (INIS)

Jeong, Chang Joon

2004-03-01

The environmental effect of the self-sufficient fast reactor scenario, which is considered as one of the full fissile plutonium and transuranic recycle scenario in Gen-IV roadmap, has been analyzed by using the dynamic analysis method. Through the parametric calculations for the fast reactor deployment time and capacity, the environmental effects of the fuel cycle for important parameters such as the amount of spent fuel and the combined amounts of plutonium and minor actinides were estimated and compared to those of the once-through LWR fuel cycle. The results of the sensitivity calculations showed that an early deployment of the fast reactor with a high capacity can reduce the accumulation of spent fuel by up to 37%. Furthermore, the recycling of plutonium and minor actinides can reduce the key repository parameter (long term decay heat). Therefore the favorable environmental effects can be expected with the implementation of the symbiotic fast reactor scenario

Neutronic design of a plutonium-thorium burner small nuclear reactor

International Nuclear Information System (INIS)

Hartanto, Donny

2010-02-01

A small nuclear reactor using thorium and plutonium fuel has been designed from the neutronic point of view. The thermal power of the reactor is 150 MWth and it is proposed to be used to supply electricity in an island in Indonesia. Thorium and plutonium fuel was chosen because in recent years the thorium fuel cycle is one of the promising ways to deal with the increasing number of plutonium stockpiles, either from the utilization of uranium fuel cycle or from nuclear weapon dismantling. A mixed fuel of thorium and plutonium will not generate the second generation of plutonium which will be a better way to incinerate the excess plutonium compared with the MOX fuel. Three kinds of plutonium grades which are the reactor grade (RG), weapon grade (WG), and spent fuel grade (SFG) plutonium, were evaluated as the thorium fuel mixture in the 17x17 Westinghouse PWR Fuel assembly. The evaluated parameters were the multiplication factor, plutonium depletion, fissile buildup, neutron spectrum, and temperature reactivity feedback. An optimization was also done to increase the plutonium depletion by changing the Moderator to Fuel Ratio (MFR). The computer codes TRITON (coupled NEWT and ORIGEN-S) in SCALE version 6 were used as the calculation tool for this assembly level. From the evaluation and optimization of the fuel assembly, the whole core was designed. The core was consisted of 2 types of thorium fuel with different plutonium grade and it followed the checkerboard loading pattern. A new concept of enriched burnable poison was also introduced to the core. The core life is 6.4 EFPY or 75 GWd/MTHM. It can burn up to 58% of its total mass of initial plutonium. VENTURE was used as the calculation tool for the core level

Fast reactors: the industrial perspective

International Nuclear Information System (INIS)

Vaughan, R.D.

1986-01-01

Industrial participation in the development of the fast reactor is reviewed, from the construction of PFR at Dounreay to the initial steps towards collaboration in Europe. The optimum design of the fast reactor has changed considerably from the days when it was needed urgently to forestall a shortage of uranium to today when uranium is abundant and cheap. The evolution of the reactor design over this period is described. Collaboration in Europe is shown to be the only answer to high development costs and the search for a reactor which will compete with thermal reactors in today's environment. The partner countries in this collaboration are all motivated differently, and this is leading to some delays in concluding the necessary agreements. The objective on the industrial front is now to participate in the two or three demonstration fast reactors that will be built in Europe during the remainder of the century leading, it is hoped, to a competitive reactor design by the year 2000. (author)

Fuel Cycle of Reactor SVBR-100

Energy Technology Data Exchange (ETDEWEB)

Zrodnikov, A.V.; Toshinsky, G.I.; Komlev, O.G. [FSUE State Scientific Center Institute for Physics and Power Engineering, 1, Bondarenko sq., Obninsk, Kaluga rg., 249033 (Russian Federation)

2009-06-15

Modular fast reactor with lead-bismuth heavy liquid-metal coolant in 100 MWe class (SVBR 100) is referred to the IV Generation reactors and shall operate in a closed nuclear fuel cycle (NFC) without consumption of natural uranium. Usually it is considered that launch of fast reactors (FR) is realized using mixed uranium-plutonium fuel. However, such launch of FRs is not economically effective because of the current costs of natural uranium and uranium enrichment servicing. This is conditioned by the fact that the quantity of reprocessing the spent nuclear fuel (SNF) of thermal reactors (TR) calculated for a ton of plutonium that determines the expenditures for construction and operation of the corresponding enterprise is very large due to low content of plutonium in the TR SNF. The economical effectiveness of FRs will be reduced as the enterprises on reprocessing the TR SNF have to be built prior to FRs have been implemented in the nuclear power (NP). Moreover, the pace of putting the FRs in the NP will be constrained by the quantity of the TR SNF. The report grounds an alternative strategy of FRs implementation into the NP, which is considered to be more economically effective. That is conditioned by the fact that in the nearest future use of the mastered uranium oxide fuel for FRs and operation in the open fuel cycle with postponed reprocessing will be most economically expedient. Changeover to the mixed uranium-plutonium fuel and closed NFC will be economically effective when the cost of natural uranium is increased and the expenditures for construction of enterprises on SNF reprocessing, re-fabrication of new fuel with plutonium and their operating becomes lower than the corresponding costs of natural uranium, uranium enrichment servicing, expenditures for fabrication of fresh uranium fuel and long temporary storage of the SNF. As when operating in the open NFC, FRs use much more natural uranium as compared with TRs, and at a planned high pace of NP development

The fast breeder reactor

International Nuclear Information System (INIS)

Collier, J.

1990-01-01

The arguments for and against the fast breeder reactor are debated. The case for the fast reactor is that the world energy demand will increase due to increasing population over the next forty years and that the damage to the global environment from burning fossil fuels which contribute to the greenhouse effect. Nuclear fission is the only large scale energy source which can achieve a cut in the use of carbon based fuels although energy conservation and renewable sources will also be important. Fast reactors produce more energy from uranium than other types of (thermal) reactors such as AGRs and PWRs. Fast reactors would be important from about 2020 onwards especially as by then many thermal reactors will need to be replaced. Fast reactors are also safer than normal reactors. The arguments against fast reactors are largely economic. The cost, especially the capital cost is very high. The viability of the technology is also questioned. (UK)

Determination of uranium and plutonium in high active solutions by extractive spectrophotometry

International Nuclear Information System (INIS)

Subba Rao, R.V.; Damodaran, K.; Santosh Kumar, G.; Ravi, T.N.

2000-01-01

Plutonium and uranium was extracted from nitric acid into trioctyl phosphine oxide in xylene. The TOPO layer was analysed by spectrophotometry. Thoron was used as the chromogenic agent for plutonium. Pyridyl azoresorcinol was used as chromogenic agent for uranium. The molar absorption coefficient for uranium and plutonium was found to be 19000 and 19264 liter/mole-cm, respectively. The correlation coefficient for plutonium and uranium was found to be 0.9994. The relative standard deviation for the determination of plutonium and uranium was found to be 0.96% and 1.4%, respectively. (author)

The Plutonium Fuel Laboratory at Studsvik and Its Activities

Energy Technology Data Exchange (ETDEWEB)

Hultgren, A.; Berggren, G.; Brown, A.; Eng, H. U.; Forsyth, R. S. [AB Atomenergi, Studsvik (Sweden)

1967-09-15

The plutonium fuel laboratory at Studsvik is engaged in development work on plutonium-enriched fuel. At present, low enriched fuel for thermal reactors is being studied: work on fuel with a higher plutonium content for fast reactors is foreseen at a later date. So far only the pellet technique is under consideration, and a number of pellet rod specimens will be produced and irradiated in the reactor R2. These specimens include pellets from both co-precipitated uranium-plutonium salts and from physically mixed oxides. Comparison of these two materials will be extended to different density levels and different heat ratings. The methods and techniques used and studied include wet chemical work for powder preparation (continuous precipitation of Pu(IV)-oxalate with oxalic acid, continuous co-precipitation of plutonium and uranium with ammonia, optimization of.precipitation conditions using U(IV) and U(VI) respectively) ; powder preparation (drying, calcination, reduction, mixing, milling, binder addition, granulation); pellet preparation (pressing, debonding, sintering, inspection): encapsulation (charging, welding of end plug, helium filling, end sealing by welding, leak detection, decontamination); metallography (specimen preparation (moulding, polishing), etching, microscopy); structure investigations (thermal analysis (TG, DTA), X-ray diffraction, neutron diffraction, data handling by computer analysis); radiometric methods (direct plutonium determination by gamma spectrometry, non-destructive burn-up analysis by high resolution gamma spectrometry, using a Ge(Li) detector) ; rework of waste (recovery of plutonium from fuel waste by extraction with trilauryl amine and anion exchange). The plutonium fuel laboratory forms part of the Active Central Laboratory. The equipment is contained in four adjacent 10 x 15 m rooms; .for diffraction work and inactive uranium work additional space is available. All the forty glove boxes in operation except two are of AB Atomenergi

Substantiation of physical concepts of fast reactors in Russia: experience and prospects

Energy Technology Data Exchange (ETDEWEB)

Alekseev, P.N. [Russian Research Center ' Kurchatov Institute' (RRC KI), 1, Kurchatov Sq., Moscow, 123182 (Russian Federation); Vasiliev, B.A. [Experimental Design Bureau of Machine Building (OKBM) 15, Burnakovskiy Pr., N. Novgorod, 603074 (Russian Federation); Kormilitsyn, M.V. [State Scientific Center of Russian Federation - Research Institute of Atomic Reactors (NIIAR) Dimitrovgrad-10, Ulianovsk Reg., 433510 (Russian Federation); Lopatkin, A.V. [N.A. Dollezhal Research and Development Institute of Power Engineering (NIKIET) 2/8, M. Krasnoselskaya Str., Moscow, 107140 (Russian Federation); Seleznev, E.F. [All-Russian Research Institute for Nuclear Power Plant Operation (VNIIAES) 25, Ferganskaya, Moscow, 109507 (Russian Federation); Khomyakov, Yu.S.; Tsybulia, A.M. [State Scientific Center of the Russian Federation - A. I. Leypunsky Institute for Physics and Power Engineering (SSC RF- IPPE) 1, Bondarenko Sq., Obninsk, Kaluga Reg., 249033 (Russian Federation); Tocheny, L.V. [International Science and Technology Center (ISTC) 32-34 Krasnoproletarskaya Ulitsa, Moscow, 127473 (Russian Federation)

2008-07-01

The fast reactor concept in Russia has accumulated unique experience, since its advent in the 1950's and up to the present, from the creation of the first experimental installation BR-1, experimental reactors BR-5 and BOR-60, the pilot industrial reactors BN-350 in Kazakhstan and up to the BN-600 at Beloyarsk Atomic Power Station. Investigations on the first experimental installations BR-1 and BR-5/-10 proved the propriety of the idea that it is possible to create nuclear reactors that can produce more nuclear fuel than they consume, i.e. the idea of breeding. The architecture of such reactors was also designed, producing a current leader among fast reactors with sodium coolant and oxide uranium-plutonium fuel. Operational experience of BOR-60, BN-350 and, particularly, BN-600 confirmed the engineering and technical feasibility of the concept of fast reactors, the possibility for its realization both for power production and for certain other purposes as well, such as desalinisation of sea water (BN-350) and for radionuclide production (BN-350, BN-600), and it enabled the development and verification of different models, computer methods and codes. The paper presents a review of experience in the creation of plants with fast reactors, scientific research on these installations, principal results, the current status of experimental data analysis, and prospective directions in the development of fast reactors and the corresponding experimental basis in Russia. (authors)

Plutonium oxides and uranium and plutonium mixed oxides. Carbon determination

International Nuclear Information System (INIS)

Anon.

Determination of carbon in plutonium oxides and uranium plutonium mixed oxides, suitable for a carbon content between 20 to 3000 ppm. The sample is roasted in oxygen at 1200 0 C, the carbon dioxide produced by combustion is neutralized by barium hydroxide generated automatically by coulometry [fr

Reactor physics and reactor strategy investigations into the fissionable material economy of the thorium and uranium cycle in fast breeder reactors and high temperature reactors

International Nuclear Information System (INIS)

Schikorr, W.M.

In this work the properties governing the fissionable material economy of the uranium and thorium cycles are investigated for the advanced reactor types currently under development - the fast breeder reactor (FBR) and the high temperature reactor (HTR) - from the point of view of the optimum utilization of the available nuclear fuel reserves and the continuance of supply of these reserves. For this purpose, the two reactor types are first of all considered individually and are subsequently discussed as a complementary overall system

New Concept of Designing Composite Fuel for Fast Reactors with Closing Fuel Cycle

International Nuclear Information System (INIS)

Savchenko, A.; Vatulin, A.; Uferov, O.; Kulakov, G.; Sorokin, V.

2013-01-01

For fast reactors a novel type of promising composite U-PuO2 fuel is proposed which is based on dispersion fuel elements. Basic approach to fuel element development - separated operations of fabricating uranium meat fuel element and introducing into it Pu or MA dioxides powder, that results in minimizing dust forming operations in fuel element fabrication. Novel fuel features higher characteristics in comparison to metallic or MOX fuel its fabrication technology is readily accomplished and is environmentally clean. A possibility is demonstrated of fabricating coated steel claddings to protect from interaction with fuel and fission products when use standard rod type MOX or metallic U-Pu-Zr fuel. Novel approach to reprocessing of composite fuel is demonstrated, which allows to separate uranium from burnt plutonium as well as the newly generated fissile plutonium from burnt one without chemical processes, which simplifies the closing of the nuclear fuel cycle. Novel composite fuel combines the advantages of metallic and ceramic types of fuel and has high uranium density that allows also to implicate it in BREST types reactor with conversion ratio more than 1. Peculiarities of closing nuclear cycle with composite fuel are demonstrated that allows more effective re-usage of generated Pu as well as, minimizing r/a wastes by incineration of MA in specially developed IMF design

Diffusion in the uranium - plutonium system and self-diffusion of plutonium in epsilon phase

International Nuclear Information System (INIS)

Dupuy, M.

1967-07-01

A survey of uranium-plutonium phase diagram leads to confirm anglo-saxon results about the plutonium solubility in α uranium (15 per cent at 565 C) and the uranium one in ζ phase (74 per cent at 565 C). Interdiffusion coefficients, for concentration lower than 15 per cent had been determined in a temperature range from 410 C to 640 C. They vary between 0.2 and 6 10 12 cm 2 s -1 , and the activation energy between 13 and 20 kcal/mole. Grain boundary, diffusion of plutonium in a uranium had been pointed out by micrography, X-ray microanalysis and α autoradiography. Self-diffusion of plutonium in ε phase (bcc) obeys Arrhenius law: D = 2. 10 -2 exp -(18500)/RT. But this activation energy does not follow empirical laws generally accepted for other metals. It has analogies with 'anomalous' bcc metals (βZr, βTi, βHf, U γ ). (author) [fr

Development of DIPRES feed for the fabrication of mixed-oxide fuels for fast breeder reactors

International Nuclear Information System (INIS)

Griffin, C.W.; Rasmussen, D.E.; Lloyd, M.H.

1983-01-01

The DIrect PREss Spheroidized feed process combines the conversion of uranium-plutonium solutions into spheres by internal gelation with conventional pellet fabrication techniques. In this manner, gel spheres could replace conventional powders as the feed material for pellet fabrication of nuclear fuels. Objective of the DIPRES feed program is to develop and qualify a process to produce mixed-oxide fuel pellets from gel spheres for fast breeder reactors. This process development includes both conversion and fabrication activities

Ultratrace analysis of uranium and plutonium by mass spectrometry

International Nuclear Information System (INIS)

Wogman, N.A.; Wacker, J.F.; Olsen, K.B.; Petersen, S.L.; Farmer, O.T.; Kelley, J.M.; Eiden, G.C.; Maiti, T.C.

2002-01-01

Full text: Uranium and plutonium have traditionally been analyzed using alpha energy spectrometry. Both isotopic compositions and elemental abundances can be characterized on samples containing microgram to milligram quantities of uranium and nanogram to microgram quantities of plutonium. In the past ten years or so, considerable interest has developed in measuring nanograms quantities of uranium and sub-picogram quantities of plutonium in environmental samples. Such measurements require high sensitivity and as a consequence, sensitive mass spectrometric-based methods have been developed. Thus, the analysis of uranium and plutonium have gone from counting decays to counting atoms, with considerable increases in both sensitivity and precision for isotopic measurements. At the Pacific Northwest National Laboratory (PNNL), we have developed highly sensitive methods to analyze uranium and plutonium in environmental samples. The development of an ultratrace analysis capability for measuring uranium and plutonium has arisen from a need to detect and characterize environmental samples for signatures associated with nuclear industry processes. Our most sensitive well-developed methodologies employ thermal ionization mass spectrometry (TIMS), however, recent advances in inductively coupled plasma mass spectrometry (ICP-MS) have shown considerable promise for use in detecting uranium and plutonium at ultratrace levels. The work at PNNL has included the development of both chemical separation and purification techniques, as well as the development of mass spectrometric instrumentation and techniques. At the heart of our methodology for TIMS analysis is a procedure that utilizes 100-microliter-volumes of analyte for chemical processing to purify, separate, and load actinide elements into resin beads for subsequent mass spectrometric analysis. The resin bead technique has been combined with a thorough knowledge of the physicochemistry of thermal ion emission to achieve

Experimental study of the higher isotopes of plutonium in the coupled fast-thermal assembly Ermine

International Nuclear Information System (INIS)

Bioux, Philippe.

1973-01-01

The most important results so far of the plutonium isotopes programme carried out in Ermine are reviewed. The results were obtained on four networks: one with uranium fuel and three with plutonium. The choice of these four networks was essentially based on the energy range of their nuclear reactions, wide enough to include the large reactor energy range, and yet realistic, with a neutron energy distribution in the 4 networks which is never very far from that encountered in a power reactor. The information relative to the high isotopes of plutonium which were obtained in these networks mostly came from: the fission indices measured in the 4 networks, the study of the balance in the two media at k(infinite)=1, reactivity measurements on cell replacements and on various plutonium samples, carried out on the three plutonium fuel networks [fr

Run-Beyond-Cladding-Breach (RBCB) test results for the Integral Fast Reactor (IFR) metallic fuels program

International Nuclear Information System (INIS)

Batte, G.L.; Hoffman, G.L.

1990-01-01

In 1984 Argonne National Laboratory (ANL) began an aggressive program of research and development based on the concept of a closed system for fast-reactor power generation and on-site fuel reprocessing, exclusively designed around the use of metallic fuel. This is the Integral Fast Reactor (IFR). Although the Experimental Breeder Reactor-II (EBR-II) has used metallic fuel since its creation 25 yeas ago, in 1985 ANL began a study of the characteristics and behavior of an advanced-design metallic fuel based on uranium-zirconium (U-Zr) and uranium-plutonium-zirconium (U-Pu-Zr) alloys. During the past five years several areas were addressed concerning the performance of this fuel system. In all instances of testing the metallic fuel has demonstrated its ability to perform reliably to high burnups under varying design conditions. This paper will present one area of testing which concerns the fuel system's performance under breach conditions. It is the purpose of this paper to document the observed post-breach behavior of this advanced-design metallic fuel. 2 figs., 1 tab

BREST-OD-300 Reactor as a prototype of the future commercial lead cooled fast reactor of natural safety

Energy Technology Data Exchange (ETDEWEB)

Orlov, V.V.; Smirnov, V.S.; Filin, A.I.; Glazov, A.G. [N.A. Dollezhal Institute ' NIKIET' , PO Box 788, Moscow, 101000 (Russian Federation)

2006-07-01

This paper briefly describes the physical and design features of a demonstration 300 MWe fast reactor with uranium-plutonium nitride fuel and lead coolant, BREST-OD-300, under development in Russia. This reactor is regarded as a prototype of future commercial reactors, which may form a foundation for large-scale growth of nuclear power in this new century. It is demonstrated that the natural properties of the lead coolant and nitride fuel combined with the physical and design features specific to fast reactors ensure natural safety of BREST and, with any credible initiating events, allow deterministic exclusion of accidents with large radioactive releases requiring evacuation of local residents. The paper identifies the ways and means of attaining natural safety, which rule out prompt criticality excursion, loss of cooling and fuel failure through use of a small reactivity margin, commensurable with {beta}{sub eff}, low pressure in the circuit, large margins to temperature limits, high natural circulation, passive decay heat removal by air unlimited in time, high heat accumulating capability of lead-filled circuit, stabilizing temperature and coolant flow rate feedbacks, etc. (authors)

BREST-OD-300 Reactor as a prototype of the future commercial lead cooled fast reactor of natural safety

International Nuclear Information System (INIS)

Orlov, V.V.; Smirnov, V.S.; Filin, A.I.; Glazov, A.G.

2006-01-01

This paper briefly describes the physical and design features of a demonstration 300 MWe fast reactor with uranium-plutonium nitride fuel and lead coolant, BREST-OD-300, under development in Russia. This reactor is regarded as a prototype of future commercial reactors, which may form a foundation for large-scale growth of nuclear power in this new century. It is demonstrated that the natural properties of the lead coolant and nitride fuel combined with the physical and design features specific to fast reactors ensure natural safety of BREST and, with any credible initiating events, allow deterministic exclusion of accidents with large radioactive releases requiring evacuation of local residents. The paper identifies the ways and means of attaining natural safety, which rule out prompt criticality excursion, loss of cooling and fuel failure through use of a small reactivity margin, commensurable with β eff , low pressure in the circuit, large margins to temperature limits, high natural circulation, passive decay heat removal by air unlimited in time, high heat accumulating capability of lead-filled circuit, stabilizing temperature and coolant flow rate feedbacks, etc. (authors)

The economics of plutonium recycle

International Nuclear Information System (INIS)

James, R.A.

1977-11-01

The individual cost components and the total fuel cycle costs for natural uranium and uranium-plutonium mixed oxide fuel cycles for CANDU-PHW reactors are discussed. A calculation is performed to establish the economic conditions under which plutonium recycle would be economically attractive. (auth)

Uranium in phosphate rocks and future nuclear power fleets

International Nuclear Information System (INIS)

Gabriel, S.; Baschwitz, A.; Mathonniere, G.

2014-01-01

According to almost all forward-looking studies, the world’s energy consumption will increase in the future decades, mostly because of the growing world population and the long-term development of emerging countries. The effort to contain global warming makes it hard to exclude nuclear energy from the global energy mix. Current light water reactors (LWR) burn fissile uranium (a natural, finite resource), whereas some future Generation IV reactors, as Sodium fast reactors (SFR), starting with an initial fissile load, will be capable of recycling their own plutonium and already-extracted depleted uranium. This makes them a feasible solution for the sustainable development of nuclear energy. Nonetheless, a sufficient quantity of plutonium is needed to start up an SFR, with the plutonium already being produced in LWR. The availability of natural uranium therefore has a direct impact on the capacity of the reactors (both LWR and SFR) that we can build. This paper discusses the correspondence between the resources and the nuclear power demand as estimated by various international organisations. Uranium is currently produced from conventional sources. The estimated quantities of uranium evolve over time in relation to their rate of extraction and the discovery of new deposits. Contrary to conventional resources, unconventional resources – because they are hardly used – also exist. These resources are more uncertain both in terms of their quantities and the feasibility of recovering them. Recovering uranium from seawater would guarantee a virtually infinite resource of nuclear fuel, but its technical and economic feasibility has yet to be demonstrated, and huge advances need to be achieved in this direction. According to different publications on phosphate reserves, the potential amount of uranium recoverable from phosphates can be estimated at around 4 MtU. Furthermore, the production of uranium as a by-product of phosphate is determined by the world production of

Fuel management of mixed reactor type power plant systems

International Nuclear Information System (INIS)

Csom, Gyula

1988-01-01

Breeding gain in symbiotic nuclear power plant system consisting of both thermal and fast breeder reactors depends on the characteristics and the ratio of thermal and fast reactors. The composition of the symbiotic power plant systems was determined for equilibrium and plutonium deficient systems. According to natural uranium utilization, symbiotic power plant systems are not less efficient than the systems containing only fast breeders. Depleted uranium can be applied in both types of systems. Reprocessing demands of the symbiotic power plant sytems were determined. (V.N.) 23 figs.; 1 tab

Comparison of actinides and fission products recycling scheme with the normal plutonium recycling scheme in fast reactors

Directory of Open Access Journals (Sweden)

Salahuddin Asif

2013-01-01

Full Text Available Multiple recycling of actinides and non-volatile fission products in fast reactors through the dry re-fabrication/reprocessing atomics international reduction oxidation process has been studied as a possible way to reduce the long-term potential hazard of nuclear waste compared to that resulting from reprocessing in a wet PUREX process. Calculations have been made to compare the actinides and fission products recycling scheme with the normal plutonium recycling scheme in a fast reactor. For this purpose, the Karlsruhe version of isotope generation and depletion code, KORIGEN, has been modified accordingly. An entirely novel fission product yields library for fast reactors has been created which has replaced the old KORIGEN fission products library. For the purposes of this study, the standard 26 groups data set, KFKINR, developed at Forschungszentrum Karlsruhe, Germany, has been extended by the addition of the cross-sections of 13 important actinides and 68 most important fission products. It has been confirmed that these 68 fission products constitute about 95% of the total fission products yield and about 99.5% of the total absorption due to fission products in fast reactors. The amount of fissile material required to guarantee the criticality of the reactor during recycling schemes has also been investigated. Cumulative high active waste per ton of initial heavy metal is also calculated. Results show that the recycling of actinides and fission products in fast reactors through the atomics international reduction oxidation process results in a reduction of the potential hazard of radioactive waste.

Fast reactors

International Nuclear Information System (INIS)

Vasile, A.

2001-01-01

Fast reactors have capacities to spare uranium natural resources by their breeding property and to propose solutions to the management of radioactive wastes by limiting the inventory of heavy nuclei. This article highlights the role that fast reactors could play for reducing the radiotoxicity of wastes. The conversion of 238 U into 239 Pu by neutron capture is more efficient in fast reactors than in light water reactors. In fast reactors multi-recycling of U + Pu leads to fissioning up to 95% of the initial fuel ( 238 U + 235 U). 2 strategies have been studied to burn actinides: - the multi-recycling of heavy nuclei is made inside the fuel element (homogeneous option); - the unique recycling is made in special irradiation targets placed inside the core or at its surroundings (heterogeneous option). Simulations have shown that, for the same amount of energy produced (400 TWhe), the mass of transuranium elements (Pu + Np + Am + Cm) sent to waste disposal is 60,9 Kg in the homogeneous option and 204.4 Kg in the heterogeneous option. Experimental programs are carried out in Phenix and BOR60 reactors in order to study the feasibility of such strategies. (A.C.)

Sodium-cooled Fast Reactor Cores using Uranium-Free Metallic Fuels for Maximizing TRU Support Ratio

International Nuclear Information System (INIS)

You, WuSeung; Hong, Ser Gi

2014-01-01

The depleted uranium plays important roles in the SFR burner cores because it substantially contributes to the inherent safety of the core through the negative Doppler coefficient and large delayed neutron. However, the use of depleted uranium as a diluent nuclide leads to a limited value of TRU support ratio due to the generation of TRUs through the breeding. In this paper, we designed sodium cooled fast reactor (SFR) cores having uranium-free fuels 3,4 for maximization of TRU consumption rate. However, the uranium-free fuelled burner cores can be penalized by unacceptably small values of the Doppler coefficient and small delayed neutron fraction. In this work, metallic fuels of TRU-(W or Ni)-Zr are considered to improve the performances of the uranium-free cores. The objective of this work is to consistently compare the neutronic performances of uranium-free sodium cooled fast reactor cores having TRU-Zr metallic fuels added with Ni or W and also to clarify what are the problematic features to be resolved. In this paper, a consistent comparative study of 400MWe sodium cooled burner cores having uranium-based fuels and uranium-free fuels was done to analyze the relative core neutronic features. Also, we proposed a uranium-free metallic fuel based on Nickel. From the results, it is found that tungsten-based uranium-free metallic fuel gives large negative Doppler coefficient due to high resonance of tungsten isotopes but this core has large sodium void worth and small effective delayed neutron fraction while the nickel-based uranium-free metallic fuelled core has less negative Doppler coefficient but smaller sodium void worth and larger effective delayed neutron fraction than the tungsten-based one. On the other hand, the core having TRU-Zr has very high burnup reactivity swing which may be problematic in compensating it using control rods and the least negative Doppler coefficient

Minimization of an initial fast reactor uranium-plutonium load by using enriched lead-208 as a coolant

Energy Technology Data Exchange (ETDEWEB)

Khorasanov, G.L. [Institute for Physics and Power Engineering named after A.I. Leypunsky, 1 Bondarenko Square, Obninsk, Kaluga Region 249033 (Russian Federation)], E-mail: khorasan@ippe.ru; Korobeynikov, V.V.; Ivanov, A.P.; Blokhin, A.I. [Institute for Physics and Power Engineering named after A.I. Leypunsky, 1 Bondarenko Square, Obninsk, Kaluga Region 249033 (Russian Federation)

2009-09-15

Long-term scenarios of nuclear energy evolution over the world scale predict deployment of fast reactors (FRs) from 2020 to 2030 and achievement on 2050 the world installed capacity equal to 1500 GW{sub e} with essential increasing the FRs number. For several countries (i.e. Russia, Japan) whose policies are based on a sharp increase of nuclear production, at the stage near 2030-2040 when plutonium, Pu, from the PWR spent nuclear fuel is consumed, the Pu lack will stimulate minimization of its load in FRs. The period of Pu deficiency will be prolonged till the years when breeding gain (BG) equal to 0.2-0.3 in fast breeding reactors (FBRs) is obtained which corresponds to Pu inventory doubling time of 44-24 years. In this paper one of opportunities to minimize fuel loading is considered: it is related to using a low neutron capturing lead isotope, {sup 208}Pb, as a FR coolant. It is known, that natural lead, {sup nat}Pb, contains a stable lead isotope, {sup 208}Pb, having a small cross-section of neutron capture via (n, {gamma}) reaction. In the paper it is shown that the macroscopic cross-sections <{sigma}{sub n,{gamma}}> of radiation neutron capture by the lead isotope {sup 208}Pb averaged on the ADS core neutron spectra are by {approx}3.7-4.5 times less than the corresponding macroscopic cross-sections for a natural mix of lead isotopes {sup nat}Pb. This circumstance allows minimizing load of a lead fast reactor (LFR) core for achievement its criticality, as well as the load of an accelerator-driven system (ADS) subcritical core-for achievement of its small subcriticality. In using {sup 208}Pb instead of {sup nat}Pb in the ADS blanket, the multiplication factor of the subsritical core, K{sub eff}, could be increased from the initial value K{sub eff} = 0.953 up to the value of K{sub eff} = 0.970. To achieve this higher value of K{sub eff} in the same core cooled by {sup nat}Pb an additional amount of 20-30% of U-Pu fuel will be needed. The isotope {sup 208}Pb

The effect of heavy water reactors and liquid fuel reactors on the long-term development of nuclear energy

International Nuclear Information System (INIS)

Brand, P.; Wiechers, W.K.

1974-01-01

The effects of the rates at which various combinations of power reactor types are installed on the long-range (to the year 2040) uranium and plutonium inventory requirements are examined. Consideration is given to light water reactors, fast breeder reactors, high temperature gas-cooled reactors, heavy water reactors, and thermal breeder reactors, in various combinations, and assuming alternatively a 3% and a 5% growth in energy demand

The fast reactor and energy supply

International Nuclear Information System (INIS)

1979-01-01

The progress made with fast reactor development in many countries is summarised showing that the aim is to provide to the nation concerned an ability to instal fast reactor power stations at the end of this century or early in the next one. Accepting the importance of fast reactors as a potential independent source of energy, problems concerning economics, industrial capability, technical factors, public acceptibility and in particular plutonium management, are discussed. It is concluded that although fast reactors have reached a comparatively advanced stage of development, a number of factors make it likely that their introduction for electricity generation will be a gradual process. Nevertheless it is necessary to complete demonstration and development phases in good time. (U.K.)

Recent developments in the dissolution and automated analysis of plutonium and uranium for safeguards measurements

International Nuclear Information System (INIS)

Jackson, D.D.; Marsh, S.F.; Rein, J.E.; Waterbury, G.R.

1975-01-01

The status of a program to develop assay methods for plutonium and uranium for safeguards purposes is presented. The current effort is directed more toward analyses of scrap-type material with an end goal of precise automated methods that also will be applicable to product materials. A guiding philosophy for the analysis of scrap-type materials, characterized by heterogeneity and difficult dissolution, is relatively fast dissolution treatment to effect 90 percent or more solubilization of the uranium and plutonium, analysis of the soluble fraction by precise automated methods, and gamma-counting assay of any residue fraction using simple techniques. A Teflon-container metal-shell apparatus provides acid dissolutions of typical fuel cycle materials at temperatures to 275 0 C and pressures to 340 atm. Gas--solid reactions at elevated temperatures separate uranium from refractory materials by the formation of volatile uranium compounds. The condensed compounds then are dissolved in acid for subsequent analysis. An automated spectrophotometer is used for the determination of uranium and plutonium. The measurement range is 1 to 14 mg of either element with a relative standard deviation of 0.5 percent over most of the range. The throughput rate is 5 min per sample. A second-generation automated instrument is being developed for the determination of plutonium. A precise and specific electroanalytical method is used as its operational basis. (auth)

Irradiation behaviour of mixed uranium-plutonium carbides, nitrides and carbonitrides; Comportement a l'irradiation de carbures, nitrures et carbonitrures mixtes d'uranium et de plutonium

Energy Technology Data Exchange (ETDEWEB)

Mikailoff, H; Mustelier, J P; Bloch, J; Leclere, J; Hayet, L [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

1967-07-01

In the framework of the research program of fast reactor fuels two irradiation experiments have been carried out on mixed uranium-plutonium carbides, nitrides and carbo-nitrides. In the first experiment carried out with thermal neutrons, the fuel consisted of sintered pellets sheathed in a stainless steel can with a small gap filled with helium. There were three mixed mono-carbide samples and the maximum linear power was 715 W/cm. After a burn-up slightly lower than 20000 MW day/tonne, a swelling of the fuel which had ruptured the cans was observed. In the second experiment carried out in the BR2 reactor with epithermal neutrons, the samples consisted of sintered pellets sodium bonded in a stainless steel tube. There were three samples containing different fuels and the linear power varies between 1130 and 1820 W/cm. Post-irradiation examination after a maximal burn-up of 1550 MW day/tonne showed that the behaviour of the three fuel elements was satisfactory. (authors) [French] Dans le cadre du programme d'etude des conibustiles pour reacteurs rapides, on a realise deux experiences d'irradiation de carbures, nitrures et carbonitrures mixtes d'uranium et de plutonium. Dans la premiere experience, faite en neutrons thermiques, le combustible etait constitue de,pastilles frittees gainees dans un tube d'acier inoxydable avec un faible jeu rempli d'helium. Il y avait trois echantillons de monocarbures mixtes, et la puissance lineaire maximale etait de 715 W/cm. Apres un taux de combustion legerement inferieur a 20 000 MWj/t, on a observe un gonflement des combustible qui a provoque, la rupture des gaines. Pans la seconde experience, realisee dans le reacteur BR2 en neutrons epithermiques, les echantillons etaient constitues de pastilles frittees gainees dans un tube d'acier avec un joint sodium. Il y avait trois echantillons contenant des combustibles differents, et la puissance lineaire variait de 1130 a 1820 W/cm. Les examens apres irradiation a un taux maximal de

Design of a Multi-Spectrum CANDU-based Reactor, MSCR, with 37-element fuel bundles using SERPENT code

International Nuclear Information System (INIS)

Hussein, M.S.; Bonin, H.W.; Lewis, B.J.; Chan, P.

2015-01-01

The burning of highly-enriched uranium and plutonium from dismantled nuclear warhead material in the new design nuclear power plants represents an important step towards nonproliferation. The blending of these highly enriched uranium and plutonium with with uranium dioxide from the spent fuel of CANDU reactors, or mixing it with depleted uranium would need a very long time to dispose of this material. Consequently, considering that more efficient transmutation of actinides occurs in fast neutron reactors, a novel Multi-Spectrum CANDU Reactor, has been designed on the basis of the CANDU6 reactor with two concentric regions. The simulations of the MSCR were carried out using the SERPENT code. The inner or fast neutron spectrum core is fuelled by different levels of enriched uranium oxides. The helium is used as a coolant in the fast neutron core. The outer or the thermal neutron spectrum core is fuelled with natural uranium with heavy water as both moderator and coolant. Both cores use 37- element fuel bundles. The size of the two cores and the percentage level of enrichment of the fresh fuel in the fast core were optimized according to the criticality safety of the whole reactor. The excess reactivity, the regeneration factor, radial and axial flux shapes of the MSCR reactor were calculated at different of the concentration of fissile isotope 235 U of uranium fuel at the fast neutron spectrum core. The effect of variation of the concentration of the fissile isotope on the fluxes in both cores at each energy bin has been studied. (author)

Design of a Multi-Spectrum CANDU-based Reactor, MSCR, with 37-element fuel bundles using SERPENT code

Energy Technology Data Exchange (ETDEWEB)

Hussein, M.S.; Bonin, H.W.; Lewis, B.J.; Chan, P., E-mail: mohamed.hussein@rmc.ca, E-mail: bonin-h@rmc.ca, E-mail: lewis-b@rmc.ca, E-mail: Paul.Chan@rmc.ca [Royal Military College of Canada, Dept. of Chemistry and Chemical Engineering, Kingston, ON (Canada)

2015-07-01

The burning of highly-enriched uranium and plutonium from dismantled nuclear warhead material in the new design nuclear power plants represents an important step towards nonproliferation. The blending of these highly enriched uranium and plutonium with with uranium dioxide from the spent fuel of CANDU reactors, or mixing it with depleted uranium would need a very long time to dispose of this material. Consequently, considering that more efficient transmutation of actinides occurs in fast neutron reactors, a novel Multi-Spectrum CANDU Reactor, has been designed on the basis of the CANDU6 reactor with two concentric regions. The simulations of the MSCR were carried out using the SERPENT code. The inner or fast neutron spectrum core is fuelled by different levels of enriched uranium oxides. The helium is used as a coolant in the fast neutron core. The outer or the thermal neutron spectrum core is fuelled with natural uranium with heavy water as both moderator and coolant. Both cores use 37- element fuel bundles. The size of the two cores and the percentage level of enrichment of the fresh fuel in the fast core were optimized according to the criticality safety of the whole reactor. The excess reactivity, the regeneration factor, radial and axial flux shapes of the MSCR reactor were calculated at different of the concentration of fissile isotope {sup 235}U of uranium fuel at the fast neutron spectrum core. The effect of variation of the concentration of the fissile isotope on the fluxes in both cores at each energy bin has been studied. (author)

Dose rate analyses for fast reactor fuel manufacturers

International Nuclear Information System (INIS)

Smith, R.C.; Strode, J.N.; Brackenbush, L.W.; Faust, L.G.

1976-01-01

An early appraisal of the radiation exposure situation in the fabrication of plutonium enriched mixed-oxide fuels for fast reactors is presented. Radiation data are presented on fuel process operations measured under actual operating conditions using plutonium containing up to 19 wt percent 240 Pu

The PRISM reactor as a possible option to deal with the british civilian plutonium stockpile

Energy Technology Data Exchange (ETDEWEB)

Fichtlscherer, Christopher [IANUS, TU Darmstadt (Germany); Friess, Friederike [IANUS, TU Darmstadt (Germany); ISR, Universitaet fuer Bodenkultur Wien (Boku) (Austria)

2017-07-01

Dealing with stocks of separated weapon-usable plutonium is a big challenge for our modern society. This work focuses on the British civil plutonium stockpiles, which amount to 103.3 tons. One option is seen in irradiating the plutonium in a fast reactor under development, namely the GE PRISM reactor. The PRISM reactor is a small modular, fast reactor which has a thermal power of 840 MW and an electrical output of 311 MW. It is intended to use MOX fuel and proponents claim, that it thus would be possible to produce clean energy, while making the plutonium proliferation resistant. A MCNP model of the reactor is built and depletion calculations with different target burnups of the fuel were conducted to check whether the burned material would fulfil the Spent-Fuel Standard. Particularly it was checked whether the spent fuel is self protecting, meaning that the dose rate does not fall below a limit of 1 Sv/h in 1 meter distance after a cooling period of 30 years. Based on the reactor model calculations the irradiation time to fulfill this limit for the spent fuel is calculated. Based on the needed target burnup, it can be verified, whether it is possible for the PRISM reactor to render the civil plutonium proliferation resistant in only 20 years as is is claimed by its proponents.

Some questions and answers concerning fast reactors

International Nuclear Information System (INIS)

Marshall, W.

1980-01-01

The theme of the lecture is the place of the fast reactor in an evolving nuclear programme. The whole question of plutonium is first considered, ie its method of production and the ways in which it can be used in the fast reactor fuel cycle. Whether fast reactors are necessary is then discussed. Their safety is examined with particular attention to those design features which are most criticised ie high volumetric power density of the core, and the use of liquid sodium as coolant. Attention is then paid to environmental and safeguard aspects. (U.K.)

A fission-fusion hybrid reactor in steady-state L-mode tokamak configuration with natural uranium

International Nuclear Information System (INIS)

Reed, Mark; Parker, Ronald R.; Forget, Benoit

2012-01-01

This work develops a conceptual design for a fusion-fission hybrid reactor operating in steady-state L-mode tokamak configuration with a subcritical natural or depleted uranium pebble bed blanket. A liquid lithium-lead alloy breeds enough tritium to replenish that consumed by the D-T fusion reaction. The fission blanket augments the fusion power such that the fusion core itself need not have a high power gain, thus allowing for fully non-inductive (steady-state) low confinement mode (L-mode) operation at relatively small physical dimensions. A neutron transport Monte Carlo code models the natural uranium fission blanket. Maximizing the fission power gain while breeding sufficient tritium allows for the selection of an optimal set of blanket parameters, which yields a maximum prudent fission power gain of approximately 7. A 0-D tokamak model suffices to analyze approximate tokamak operating conditions. This fission blanket would allow the fusion component of a hybrid reactor with the same dimensions as ITER to operate in steady-state L-mode very comfortably with a fusion power gain of 6.7 and a thermal fusion power of 2.1 GW. Taking this further can determine the approximate minimum scale for a steady-state L-mode tokamak hybrid reactor, which is a major radius of 5.2 m and an aspect ratio of 2.8. This minimum scale device operates barely within the steady-state L-mode realm with a thermal fusion power of 1.7 GW. Basic thermal hydraulic analysis demonstrates that pressurized helium could cool the pebble bed fission blanket with a flow rate below 10 m/s. The Brayton cycle thermal efficiency is 41%. This reactor, dubbed the Steady-state L-mode non-Enriched Uranium Tokamak Hybrid (SLEUTH), with its very fast neutron spectrum, could be superior to pure fission reactors in terms of breeding fissile fuel and transmuting deleterious fission products. It would likely function best as a prolific plutonium breeder, and the plutonium it produces could actually be more

[Present conceptions of the C.E.A. concerning] the development of fast neutron reactors in France; [Les conceptions actuelles du C.E.A. concernant] la filiere des reacteurs a neutrons rapides en France

Energy Technology Data Exchange (ETDEWEB)

Vendryes, G; Gaussens, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires; Pasquer, R [Electricite de France (EDF), 75 - Paris (France)

1964-07-01

1 - The position of fast neutron reactors in the French nuclear energy program. In developing a program based on natural uranium, France will have an important stock of plutonium rich in higher isotopes. The existence of this plutonium and of the depleted uranium arising from the same reactors, has, as a logical consequence, the use of both in fast neutron reactors. Justified by this short term interest, the achievement of fast neutron reactors does, moreover, provide for a future necessity. 2 - Description of a fast neutron central power station of 1000 MWe. We indicate the characteristics of a future fast neutron central power station, plutonium fuelled, and sodium cooled. However uncertain these characteristics may be, they constitute a necessary guide in the orientation of our work. 3 - Studies carried out up to the present time. We give an outline of those studies, often very preliminary, which have given the characteristics cited above. The principal technical areas taken up are the following: - Neutronics (critical masses, breeding ratios, enrichments, flattening of the neutron flux, coefficients of reactivity, reactivity changes as a function of irradiation). - Dynamics, control, and safety. - Technology (design of the core and vessel, of the sodium system, and of the fuel handling mechanisms). These technical studies are complemented by economic considerations. The choice of the optimum characteristics is related to the existence of power production programs, and, in these programs, to the existence of plutonium producing thermal reactors. It is shown how, in this context, the existence of plutonium should be taken into account, and, in addition which mechanisms relate the economics of this plutonium to the choice of the most important parameters of the breeder reactors. 4 - Prototype reactor. The interest in an intermediate stage consisting of a reactor of a power level of about 80 MWe is justified. Its essential characteristics are briefly presented

The benefits of a fast reactor closed fuel cycle in the UK

International Nuclear Information System (INIS)

Gregg, R.; Hesketh, K.

2013-01-01

The work has shown that starting a fast reactor closed fuel cycle in the UK, requires virtually all of Britain's existing and future PWR spent fuel to be reprocessed, in order to obtain the plutonium needed. The existing UK Pu stockpile is sufficient to initially support only a modest SFR 'closed' fleet assuming spent fuel can be reprocessed shortly after discharge (i.e. after two years cooling). For a substantial fast reactor fleet, most Pu will have to originate from reprocessing future spent PWR fuel. Therefore, the maximum fast reactor fleet size will be limited by the preceding PWR fleet size, so scenarios involving fast reactors still require significant quantities of uranium ore indirectly. However, once a fast reactor fuel cycle has been established, the very substantial quantities of uranium tails in the UK would ensure there is sufficient material for several centuries. Both the short and long term impacts on a repository have been considered in this work. Over the short term, the decay heat emanating from the HLW and spent fuel will limit the density of waste within a repository. For scenarios involving fast reactors, the only significant heat bearing actinide content will be present in the final cores, resulting in a 50% overall reduction in decay energy deposited within the repository when compared with an equivalent open fuel cycle. Over the longer term, radiological dose becomes more important. Total radiotoxicity (normalised by electricity generated) is lower for scenarios with Pu recycle after 2000 years. Scenarios involving fast reactors have the lowest radiotoxicity since the quantities of certain actinides (Np, Pu and Am) eventually stabilise. However, total radiotoxicity as a measure of radiological risk does not account for differences in radionuclide mobility once in repository. Radiological dose is dominated by a small number of fission products so is therefore not affected significantly by reactor type or recycling strategy (since the

Conceptual design study on very small long-life gas cooled fast reactor using metallic natural Uranium-Zr as fuel cycle input

International Nuclear Information System (INIS)

Monado, F.; Permana, S.

2013-01-01

Full-text: A conceptual design study of very small 350 MWth Gas-cooled Fast Reactors with Helium coolant has been performed. In this study Modified CANDLE burn-up scheme was implemented to create small and long life fast reactors with natural Uranium as fuel cycle input. Such system can utilize natural Uranium resources efficiently without the necessity of enrichment plant or reprocessing plant. The core with metallic fuel based was subdivided into 10 regions with the same volume. The fresh Natural Uranium is initially put in region-1, after one cycle of 10 years of burn-up it is shifted to region-2 and the each region-1 is filled by fresh Natural Uranium fuel. This concept is basically applied to all axial regions. The reactor discharge burn-up is 31.8 % HM. From the neutronic point of view, this design is in compliance with good performance. (author)

Conceptual design study on very small long-life gas cooled fast reactor using metallic natural Uranium-Zr as fuel cycle input

International Nuclear Information System (INIS)

Monado, Fiber; Ariani, Menik; Su'ud, Zaki; Waris, Abdul; Basar, Khairul; Permana, Sidik; Aziz, Ferhat; Sekimoto, Hiroshi

2014-01-01

A conceptual design study of very small 350 MWth Gas-cooled Fast Reactors with Helium coolant has been performed. In this study Modified CANDLE burn-up scheme was implemented to create small and long life fast reactors with natural Uranium as fuel cycle input. Such system can utilize natural Uranium resources efficiently without the necessity of enrichment plant or reprocessing plant. The core with metallic fuel based was subdivided into 10 regions with the same volume. The fresh Natural Uranium is initially put in region-1, after one cycle of 10 years of burn-up it is shifted to region-2 and the each region-1 is filled by fresh Natural Uranium fuel. This concept is basically applied to all axial regions. The reactor discharge burn-up is 31.8% HM. From the neutronic point of view, this design is in compliance with good performance

Plutonium

International Nuclear Information System (INIS)

Anon.

1995-01-01

Plutonium, which was obtained and identified for the first time in 1941 by chemist Glenn Seaborg - through neutron irradiation of uranium 238 - is closely related to the history of nuclear energy. From the very beginning, because of the high radiotoxicity of plutonium, a tremendous amount of research work has been devoted to the study of the biological effects and the consequences on the environment. It can be said that plutonium is presently one of the elements, whose nuclear and physico-chemical characteristics are the best known. The first part of this issue is a survey of the knowledge acquired on the subject, which emphasizes the sanitary effects and transfer into the environment. Then the properties of plutonium related to energy generation are dealt with. Fissionable, like uranium 235, plutonium has proved a high-performance nuclear fuel. Originally used in breeder reactors, it is now being more and more widely recycled in light water reactors, in MOX fuel. Reprocessing, recycling and manufacturing of these new types of fuel, bound of become more and more widespread, are now part of a self-consistent series of operations, whose technical, economical, industrial and strategical aspects are reviewed. (author)

The passive nondestructive assay of the plutonium content of spent-fuel assemblies from the BN-350 fast-breeder reactor in the city of Aqtau, Kazakhstan

CERN Document Server

Lestone, J P; Rennie, J A; Sprinkle, J K; Staples, P; Grimm, K N; Hill, R N; Cherradi, I; Islam, N; Koulikov, J; Starovich, Z

2002-01-01

The International Atomic Energy Agency is presently interested in developing equipment and techniques to measure the plutonium content of breeder reactor spent-fuel assemblies located in storage ponds before they are relocated to more secure facilities. We present the first quantitative nondestructive assay of the plutonium content of fast-breeder reactor spent-fuel assemblies while still underwater in their facility storage pond. We have calibrated and installed an underwater neutron coincidence counter (Spent Fuel Coincidence Counter (SFCC)) in the BN-350 reactor spent-fuel pond in Aqtau, Kazakhstan. A procedure has been developed to convert singles and doubles (coincidence) neutron rates observed by the SFCC into the total plutonium content of a given BN-350 spent-fuel assembly. The plutonium content has been successfully determined for spent-fuel assemblies with a contact radiation level as high as approx 10 sup 5 Rads/h. Using limited facility information and multiple measurements along the length of spe...

Reactor-Based Plutonium Disposition: Opportunities, Options, and Issues

International Nuclear Information System (INIS)

Greene, S.R.

1999-01-01

The end of the Cold War has created a legacy of surplus fissile materials (plutonium and highly enriched uranium) in the United States (U.S.) and the former Soviet Union. These materials pose a danger to national and international security. During the past few years, the U.S. and Russia have engaged in an ongoing dialog concerning the safe storage and disposition of surplus fissile material stockpiles. In January 1997, the Department of Energy (DOE) announced the U. S. would pursue a dual track approach to rendering approximately 50 metric tons of plutonium inaccessible for use in nuclear weapons. One track involves immobilizing the plutonium by combining it with high-level radioactive waste in glass or ceramic ''logs''. The other method, referred to as reactor-based disposition, converts plutonium into mixed oxide (MOX) fuel for nuclear reactors. The U.S. and Russia are moving ahead rapidly to develop and demonstrate the technology required to implement the MOX option in their respective countries. U.S. MOX fuel research and development activities were started in the 1950s, with irradiation of MOX fuel rods in commercial light water reactors (LWR) from the 1960s--1980s. In all, a few thousand MOX fuel rods were successfully irradiated. Though much of this work was performed with weapons-grade or ''near'' weapons-grade plutonium--and favorable fuel performance was observed--the applicability of this data for licensing and use of weapons-grade MOX fuel manufactured with modern fuel fabrication processes is somewhat limited. The U.S. and Russia are currently engaged in an intensive research, development, and demonstration program to support implementation of the MOX option in our two countries. This paper focuses on work performed in the U.S. and provides a brief summary of joint U.S./Russian work currently underway

Reactor-based plutonium disposition: Opportunities, options, and issues

International Nuclear Information System (INIS)

Greene, S.

2000-01-01

The end of the Cold War has created a legacy of surplus fissile materials (plutonium and highly enriched uranium) in the United States (U.S.) and the former Soviet Union. These materials pose a danger to national and international security. During the past few years, the U.S. and Russia have engaged in an ongoing dialog concerning the safe storage and disposition of surplus fissile material stockpiles. In January 1997, the Department of Energy (DOE) announced the U.S. would pursue a dual track approach to rendering approximately 50 metric tons of plutonium inaccessible for use in nuclear weapons. One track involves immobilizing the plutonium by combining it with high-level radioactive waste in glass or ceramic ''logs''. The other method, referred to as reactor-based disposition, converts plutonium into mixed oxide (MOX) fuel for nuclear reactors. The U.S. and Russia are moving ahead rapidly to develop and demonstrate the technology required to implement the MOX option in their respective countries. U.S. MOX fuel research and development activities were started in the 1950s with irradiation of MOX fuel rods in commercial light water reactors (LWR) from the 1960s-1980s. In all, a few thousand MOX fuel rods were successfully irradiated. Though much of this work was performed with weapons-grade or ''near'' weapons-grade plutonium - and favorable fuel performance was observed - the applicability of this data for licensing and use of weapons-grade MOX fuel manufactured with modem fuel fabrication processes is somewhat limited. The U.S. and Russia are currently engaged in an intensive research, development, and demonstration program to support implementation of the MOX option in our two countries. This paper focuses on work performed in the U.S. and provides a brief summary of joint U.S./Russian work currently underway. (author)

A high temperature reactor could be used to eliminate the Russian military plutonium

International Nuclear Information System (INIS)

Foucher, N.

1999-01-01

The GT-MHR reactor (Gas Turbine Modular Helium Reactor) aims the double objective to eliminate the Russian plutonium coming from weapons, ( until 3 tons by year) and to produce a competitive energy from a small-scale power reactor with a nuclear fuel that can be of different type (plutonium or uranium). This reactor has several advantages: a high yield (47%) as every high temperature reactor and to be used in combined cycle, a high level of safety because of its ability to evacuate the residual power in a totally passive way and because of the nature of its fuel that is made of ceramics with a very high melting point that is to say no possibility of core melt. The fission products are contained in the ceramics so that reactor cannot disseminate radioactivity in its structure and consequently does not induce irradiation for the personnel. (N.C.)

Sequential potentiometric determination of uranium and plutonium in a single aliquot

International Nuclear Information System (INIS)

Rao, V.K.; Charyulu, M.M.; Natarajan, P.R.

1983-01-01

A method is reported for sequential potentiometric determination of uranium and plutonium present is an aliquot. Plutonium is first determined by oxidizing it to the hexavalent state with perchloric acid followed by iron(II) reduction and titration of excess ferrous iron with chromium(VI). Uranium is subsequently determined by reduction to the quadrivalent state using titanium(III) and titration with vanadium(V). The interference of plutonium and iron(II) is eliminated by the addition of a mixture containing sulfamic acid, nitric acid, and molybdenum(VI). The results of the analysis of mixture containing 3-5 mg quantities of uranium and plutonium are reliable with errors less than 0.3% and 0.2%, respectively. The application of the method for the analysis of mixtures containing various amounts of uranium and plutonium has been examined. (author)

Irradiated uranium reprocessing, Final report I-VI, IV Deo IV - Separation of uranium, plutonium and fission products from the irradiated fuel of the reactor in Vinca; Prerada ozracenog urana. Zavrsni izvestaj - I-VI, IV Deo - Odvajanje urana, plutonijuma i fisionih produkata iz isluzenog goriva reaktora u Vinci

Energy Technology Data Exchange (ETDEWEB)

Gal, I [Institute of Nuclear Sciences Boris Kidric, Laboratorija za visoku aktivnost, Vinca, Beograd (Serbia and Montenegro)

1961-12-15

This study describes the technology for separation of uranium, plutonium and fission products from the radioactive water solution which is obtained by dissolving the spent uranium fuel from the reactor in Vinca. The procedure should be completed in a hot cell, with the maximum permitted activity of 10 Ci.

Feasibility study of plutonium recycling in light water reactors

International Nuclear Information System (INIS)

Tabuchi, Hideoto

1979-01-01

The feasibility of plutonium recycling in light water reactors has been studied by the Agency of Natural Resources and Energy, MITI. As the first step of the feasibility study, it was planned to charge two fuel assemblies, containing uranium-plutonium mixed oxide (MO 2 ), in the core of the Tsuruga nuclear power plant (BWR) for testing. The design of fuel the safety of these fuel and the operating characteristics of these special fuel assemblies were evaluated. The specifications of MO 2 fuel pin and fuel assembly are compared to those of present uranium oxide (UO 2 ) fuel. The weight of fissile plutonium in one MO 2 fuel assembly is 2.22 kg. The characteristics of MO 2 fuel assemblies, such as reactivity, control rod worth and power distribution can be kept similar to UO 2 fuel. The plutonium isotope ratio of the MO 2 fuel is assumed as that obtained in the fuel taken out of the Tokai No. 1 gas cooled reactor. The temperature distribution in the fuel pellets is shown, compared to that of UO 2 fuel. The linear power density is 440 w/cm at the beginning of the fuel life and 360 w/cm after the burn-up of 44,000 Mwd/t. The stress in the cladding tubes of MO 2 fuel is not different from that of UO 2 fuel. The pellet-cladding interaction (PCM1) was analyzed, utilizing the FEM code, FEAST. Concerning the calculation of resonance absorption, the space dependence of thermal neutron spectra and the nuclear behavior of hollow pellets the methods of design calculation were checked up. It was recognized that regarding the nuclear characteristics of MO 2 fuel, no special technical question remains. (Nakai, Y.)

Process for recovery of plutonium from fabrication residues of mixed fuels consisting of uranium oxide and plutonium oxide

International Nuclear Information System (INIS)

Heremanns, R.H.; Vandersteene, J.J.

1983-01-01

The invention concerns a process for recovery of plutonium from fabrication residues of mixed fuels consisting of uranium oxide and plutonium oxide in the form of PuO 2 . Mixed fuels consisting of uranium oxide and plutonium oxide are being used more and more. The plants which prepare these mixed fuels have around 5% of the total mass of fuels as fabrication residue, either as waste or scrap. In view of the high cost of plutonium, it has been attempted to recover this plutonium from the fabrication residues by a process having a purchase price lower than the price of plutonium. The problem is essentially to separate the plutonium, the uranium and the impurities. The residues are fluorinated, the UF 6 and PuF 6 obtained are separated by selective absorption of the PuF 6 on NaF at a temperature of at least 400 0 C, the complex obtained by this absorption is dissolved in nitric acid solution, the plutonium is precipitated in the form of plutonium oxalate by adding oxalic acid, and the precipitated plutonium oxalate is calcined

Strategies for denaturing the weapons-grade plutonium stockpile

International Nuclear Information System (INIS)

Buckner, M.R.; Parks, P.B.

1992-10-01

In the next few years, approximately 50 metric tons of weapons-grade plutonium and 150 metric tons of highly-enriched uranium (HEU) may be removed from nuclear weapons in the US and declared excess. These materials represent a significant energy resource that could substantially contribute to our national energy requirements. HEU can be used as fuel in naval reactors, or diluted with depleted uranium for use as fuel in commercial reactors. This paper proposes to use the weapons-grade plutonium as fuel in light water reactors. The first such reactor would demonstrate the dual objectives of producing electrical power and denaturing the plutonium to prevent use in nuclear weapons

Actinide Oxidation State and O/M Ratio in Hypostoichiometric Uranium-Plutonium-Americium U0.750Pu0.246Am0.004O2-x Mixed Oxides.

Science.gov (United States)

Vauchy, Romain; Belin, Renaud C; Robisson, Anne-Charlotte; Lebreton, Florent; Aufore, Laurence; Scheinost, Andreas C; Martin, Philippe M

2016-03-07

Innovative americium-bearing uranium-plutonium mixed oxides U1-yPuyO2-x are envisioned as nuclear fuel for sodium-cooled fast neutron reactors (SFRs). The oxygen-to-metal (O/M) ratio, directly related to the oxidation state of cations, affects many of the fuel properties. Thus, a thorough knowledge of its variation with the sintering conditions is essential. The aim of this work is to follow the oxidation state of uranium, plutonium, and americium, and so the O/M ratio, in U0.750Pu0.246Am0.004O2-x samples sintered for 4 h at 2023 K in various Ar + 5% H2 + z vpm H2O (z = ∼ 15, ∼ 90, and ∼ 200) gas mixtures. The O/M ratios were determined by gravimetry, XAS, and XRD and evidenced a partial oxidation of the samples at room temperature. Finally, by comparing XANES and EXAFS results to that of a previous study, we demonstrate that the presence of uranium does not influence the interactions between americium and plutonium and that the differences in the O/M ratio between the investigated conditions is controlled by the reduction of plutonium. We also discuss the role of the homogeneity of cation distribution, as determined by EPMA, on the mechanisms involved in the reduction process.

Status of national programmes on fast breeder reactors. Twenty-fifth annual meeting of the International Working Group on Fast Reactors. Summary report. Working material

Energy Technology Data Exchange (ETDEWEB)

NONE

1992-07-01

At present nuclear power accounts for approximately 17% of total electricity generation worldwide. Given continuing population growth and the needs of the third world and developing countries to improve their economic performance and standard of living, energy demand is expected to continue to grow through the 21st century. The proportion of energy supplied as electricity is also expected to continue to increase. Although fossil fuelled electricity generation is the option preferred by several countries for the short term, there are rising concerns over climatic consequences caused by extended burning of fossil fuels as a result of the demands of a fast expanding world population. In this situation nuclear electricity will become more and more important and the known reserves of uranium would be consumed quite quickly by thermal reactors. It would be possible to sustain a large nuclear programme only by introducing fast reactors. One can conclude that there are strategic reasons for pursuing the development of fast breeder reactors. It will become desirable essential, to have this technology available for introduction. The experience of the various prototypes presently in operation has confirmed the operability and benign characteristics of the LMFR and has given ground for confidence in the future. Current fast reactor designs offer very large margins of safety and by virtue of redundant and diverse safety systems the potential for an energetic core disruptive accident or for fast reactor core meltdown has been essentially eliminated. Several international forums reviewed the current trends in the fast reactor development. The view was reaffirmed that fast breeder reactors still remain the most practical tool for effective utilization of uranium resources for the future energy needs. Achievement of competitiveness with LMRs is still the first priority condition for the future deployment of this type of reactor. The recycling of plutonium into LMFBRs would allow

Status of national programmes on fast breeder reactors. Twenty-fifth annual meeting of the International Working Group on Fast Reactors. Summary report. Working material

International Nuclear Information System (INIS)

1992-01-01

At present nuclear power accounts for approximately 17% of total electricity generation worldwide. Given continuing population growth and the needs of the third world and developing countries to improve their economic performance and standard of living, energy demand is expected to continue to grow through the 21st century. The proportion of energy supplied as electricity is also expected to continue to increase. Although fossil fuelled electricity generation is the option preferred by several countries for the short term, there are rising concerns over climatic consequences caused by extended burning of fossil fuels as a result of the demands of a fast expanding world population. In this situation nuclear electricity will become more and more important and the known reserves of uranium would be consumed quite quickly by thermal reactors. It would be possible to sustain a large nuclear programme only by introducing fast reactors. One can conclude that there are strategic reasons for pursuing the development of fast breeder reactors. It will become desirable essential, to have this technology available for introduction. The experience of the various prototypes presently in operation has confirmed the operability and benign characteristics of the LMFR and has given ground for confidence in the future. Current fast reactor designs offer very large margins of safety and by virtue of redundant and diverse safety systems the potential for an energetic core disruptive accident or for fast reactor core meltdown has been essentially eliminated. Several international forums reviewed the current trends in the fast reactor development. The view was reaffirmed that fast breeder reactors still remain the most practical tool for effective utilization of uranium resources for the future energy needs. Achievement of competitiveness with LMRs is still the first priority condition for the future deployment of this type of reactor. The recycling of plutonium into LMFBRs would allow

Qualitative chemical analysis of plutonium by Alpha spectroscopy

International Nuclear Information System (INIS)

Ramirez G, J Qumica.J.

1994-01-01

In this work the separation and purification of plutonium from irradiated uranium was done. The plutonium, produced by the irradiation of uranium in a nuclear reactor and the β decay of 239 Np, was stabilized to Pu +4 with sodium nitrite. Plutonium was separated from the fission products and uranium by ion exchange using the resin Ag 1 X 8. It was electrodeposited on stainless steel discs and the alpha radioactivity of plutonium was measured in a surface barrier detector. The results showed that plutonium was separated with a radiochemical purity higher than 99 %. (Author)

Nonproliferation and safeguards aspects of fuel cycle programs in reduction of excess separated plutonium and high-enriched uranium

International Nuclear Information System (INIS)

Persiani, P.J.

1995-01-01

The purpose of this preliminary investigation is to explore alternatives and strategies aimed at the gradual reduction of the excess inventories of separated plutonium and high-enriched uranium (HEU) in the civilian nuclear power industry. The study attempts to establish a technical and economic basis to assist in the formation of alternative approaches consistent with nonproliferation and safeguards concerns. Reference annual mass flows and inventories for a representative 1,400 Mwe Pressurized Water Reactor (PWR) fuel cycle have been investigated for three cases: the 100 percent uranium oxide UO 2 fuel loading once through cycle, and the 33 percent mixed oxide MOX loading configuration for a first and second plutonium recycle. The analysis addresses fuel cycle developments; plutonium and uranium inventory and flow balances; nuclear fuel processing operations; UO 2 once-through and MOX first and second recycles; and the economic incentives to draw-down the excess separated plutonium stores. The preliminary analysis explores several options in reducing the excess separated plutonium arisings and HEU, and the consequences of the interacting synergistic effects between fuel cycle processes and isotopic signatures of nuclear materials on nonproliferation and safeguards policy assessments

Recycling of nuclear matters. Myths and realities. Calculation of recycling rate of the plutonium and uranium produced by the French channel of spent fuel reprocessing

International Nuclear Information System (INIS)

Coeytaux, X.; Schneider, M.

2000-05-01

The recycling rate of plutonium and uranium are: from the whole of the plutonium separated from the spent fuel ( inferior to 1% of the nuclear matter content) attributed to France is under 50% (under 42 tons on 84 tons); from the whole of plutonium produced in the French reactors is less than 20% (42 tons on 224 tons); from the whole of the uranium separated from spent fuels attributed to France is about 10 % (1600 tons on 16000 tons); from the whole of the uranium contained in the spent fuel is slightly over 5%. (N.C.)

Radiological impact of plutonium recycle in the fuel cycle of LWR type reactors: professional exposure during mormal operation

International Nuclear Information System (INIS)

White, I.F.; Kelly, G.N.

1983-01-01

The radiological impact of the fuel cycle of light water type reactors using enriched uranium may be changed by plutonium recycle. The impact on human population and on the persons professionally exposed may be different according to the different steps of the fuel cycle. This report analyses the differential radiological impact on the different types of personnel involed in the fuel cycle. Each step of the fuel cycle is separately studied (fuel fabrication, reactor operation, fuel reprocessing), as also the transport of the radioactive materials between the different steps. For the whole fuel cycle, one estimates that, with regard to the fuel cycle using enriched uranium, the plutonium recycle involves a small increase of the professional exposure

Revision of the second basic plans of power reactor development in Power Reactor and Nuclear Fuel Development Corporation

International Nuclear Information System (INIS)

1978-01-01

Revision of the second basic plans concerning power reactor development in PNC (Power Reactor and Nuclear Fuel Development Corporation) is presented. (1) Fast breeder reactors: As for the experimental fast breeder reactor, after reaching the criticality, the power is raised to 50 MW thermal output within fiscal 1978. The prototype fast breeder reactor is intended for the electric output of 200 MW -- 300 MW, using mixed plutonium/uranium oxide fuel. Along the above lines, research and development will be carried out on reactor physics, sodium technology, machinery and parts, nuclear fuel, etc. (2) Advanced thermal reactor: The prototype advanced thermal reactor, with initial fuel primarily of slightly enriched uranium and heavy water moderation and boiling water cooling, of 165 MW electric output, is brought to its normal operation by the end of fiscal 1978. Along the above lines, research and development will be carried out on reactor physics, machinery and parts, nuclear fuel, etc. (Mori, K

Reactor physics studies in the GCFR phase-II critical assembly

International Nuclear Information System (INIS)

Pond, R.B.

1976-09-01

The reactor physics studies performed in the gas cooled fast reactor (GCFR) mockup on ZPR-9 are covered. This critical assembly, designated Phase II in the GCFR program, had a single zone PuO 2 -UO 2 core composition and UO 2 radial and axial blankets. The assembly was built both with and without radial and axial stainless steel reflectors. The program included the following measurements: small-sample reactivity worths of reactor constituent materials (including helium); 238 U Doppler effect; uranium and plutonium reaction rate distributions; thorium, uranium, and plutonium α and reactor kinetics. Analysis of the measurements used ENDF/B-IV nuclear data; anisotropic diffusion coefficients were used to account for neutron streaming effects. Comparison of measurements and calculations to GCFR Phase I are also made

Fast mixed spectrum reactor concept

International Nuclear Information System (INIS)

Kouts, H.J.C.; Fischer, G.J.; Cerbone, R.J.

1979-04-01

The Fast Mixed Spectrum Reactor is a highly promising concept for a fast reactor with improved features of proliferation resistance, and excellent utilization of uranium resources. In technology, it can be considered to be a branch of fast breeder development, though its operation and implications are different from those of FBR'S in important respects. Successful development programs are required in several areas to bring FMSR to reality, but the payoff from a successful program can be high

Development of UO2/PuO2 dispersed in uranium matrix CERMET fuel system for fast reactors

International Nuclear Information System (INIS)

Sinha, V.P.; Hegde, P.V.; Prasad, G.J.; Pal, S.; Mishra, G.P.

2012-01-01

CERMET fuel with either PuO 2 or enriched UO 2 dispersed in uranium metal matrix has a strong potential of becoming a fuel for the liquid metal cooled fast breeder reactors (LMR’s). In fact it may act as a bridge between the advantages and disadvantages associated with the two extremes of fuel systems (i.e. ceramic fuel and metallic fuel) for fast reactors. At Bhabha Atomic Research Centre (BARC), R and D efforts are on to develop this CERMET fuel by powder metallurgy route. This paper describes the development of flow sheet for preparation of UO 2 dispersed in uranium metal matrix pellets for three different compositions i.e. U–20 wt%UO 2 , U–25 wt%UO 2 and U–30 wt%UO 2 . It was found that the sintered pellets were having excellent integrity and their linear mass was higher than that of carbide fuel pellets used in Fast Breeder Test Reactor programme (FBTR) in India. The pellets were characterized by X-ray diffraction (XRD) technique for phase analysis and lattice parameter determination. The optical microstructures were developed and reported for all the three different U–UO 2 compositions.

Development of UO2/PuO2 dispersed in uranium matrix CERMET fuel system for fast reactors

Science.gov (United States)

Sinha, V. P.; Hegde, P. V.; Prasad, G. J.; Pal, S.; Mishra, G. P.

2012-08-01

CERMET fuel with either PuO2 or enriched UO2 dispersed in uranium metal matrix has a strong potential of becoming a fuel for the liquid metal cooled fast breeder reactors (LMR's). In fact it may act as a bridge between the advantages and disadvantages associated with the two extremes of fuel systems (i.e. ceramic fuel and metallic fuel) for fast reactors. At Bhabha Atomic Research Centre (BARC), R & D efforts are on to develop this CERMET fuel by powder metallurgy route. This paper describes the development of flow sheet for preparation of UO2 dispersed in uranium metal matrix pellets for three different compositions i.e. U-20 wt%UO2, U-25 wt%UO2 and U-30 wt%UO2. It was found that the sintered pellets were having excellent integrity and their linear mass was higher than that of carbide fuel pellets used in Fast Breeder Test Reactor programme (FBTR) in India. The pellets were characterized by X-ray diffraction (XRD) technique for phase analysis and lattice parameter determination. The optical microstructures were developed and reported for all the three different U-UO2 compositions.

International collaborations about fuel studies for reactor recycling of military quality plutonium

International Nuclear Information System (INIS)

Bernard, H.; Chaudat, J.P.

1997-01-01

In November 1992, an agreement was signed between the French and Russian governments to use in Russia and for pacific purposes the plutonium recovered from the Russian nuclear weapons dismantling. This plutonium will be transformed into mixed oxide fuels (MOX) for nuclear power production. The French Direction of Military Applications (DAM) of the CEA is the operator of the French-Russian AIDA program. The CEA Direction of Fuel Cycle (DCC) and Direction of Nuclear Reactors (DRN) are involved in the transformation of metallic plutonium into sinterable oxide powder for MOX fuel manufacturing. The Russian TOMOX (Treatment of MOX powder Metallic Objects) and DEMOX (MOX Demonstration) plants will produce the MOX fuel assemblies for the 4 VVER 1000 reactors of Balakovo and the fast BN 600 reactor. The second part of the program will involve the German Siemens and GRS companies for the safety studies of the reactors and fuel cycle plants. The paper gives also a brief analysis of the US policy concerning the military plutonium recycling. (J.S.)

Nuclear data for advanced fast reactors

International Nuclear Information System (INIS)

Rabotnov, N.S.

2001-01-01

Interest revives to fast reactors as the only proven technology obviously able of satisfying human energy needs for the next millennium by using full energy content of both natural uranium resources and of vast stocks of depleted uranium. This interest stimulates revision and improvement of fast reactor ND. Progress in reactor calculations accuracy due to better codes and much faster computers also increases relative importance of the input data uncertainties, especially in case of small reactivity margin and fuels of equilibrium compositions. The main objects of corresponding R and D efforts should be minor actinides and heavy liquid metal coolant. Data error bands and covariance information also gain importance as necessary components of neutron physics calculations. (author)

Weapons-grade plutonium dispositioning. Volume 1: Executive summary

International Nuclear Information System (INIS)

Parks, D.L.; Sauerbrun, T.J.

1993-06-01

The Secretary of Energy requested the National Academy of Sciences (NAS) Committee on International Security and Arms Control to evaluate dispositioning options for weapons-grade plutonium. The Idaho National Engineering Laboratory (INEL) assisted NAS in this evaluation by investigating the technical aspects of the dispositioning options and their capability for achieving plutonium annihilation levels greater than 90%. Additionally, the INEL investigated the feasibility of using plutonium fuels (without uranium) for disposal in existing light water reactors and provided a preconceptual analysis for a reactor specifically designed for destruction of weapons-grade plutonium. This four-volume report was prepared for NAS to document the findings of these studies. Volume 2 evaluates 12 plutonium dispositioning options. Volume 3 considers a concept for a low-temperature, low-pressure, low-power-density, low-coolant-flow-rate light water reactor that quickly destroys plutonium without using uranium or thorium. This reactor concept does not produce electricity and has no other mission than the destruction of plutonium. Volume 4 addresses neutronic performance, fabrication technology, and fuel performance and compatibility issues for zirconium-plutonium oxide fuels and aluminum-plutonium metallic fuels. This volumes gives summaries of Volumes 2--4

Simulation and control synthesis for a pulse column separation system for plutonium--uranium recovery

International Nuclear Information System (INIS)

McCutcheon, E.B.

1975-05-01

Control of a plutonium-uranium partitioning column was studied using a mathematical model developed to simulate the dynamic response and to test postulated separation mechanisms. The column is part of a plutonium recycle flowsheet developed for the recovery of plutonium and uranium from metallurgical scrap. In the first step of the process, decontamination from impurities is achieved by coextracting plutonium and uranium in their higher oxidation states. In the second step, reduction of the plutonium to a lower oxidation state allows partitioning of the plutonium and uranium. The use of hydroxylamine for the plutonium reduction in this partitioning column is a unique feature of the process. The extraction operations are carried out in pulse columns. (U.S.)

Fast breeder reactors--lecture 4

International Nuclear Information System (INIS)

Marshall, W.; Davies, L.M.

1986-01-01

This paper discusses the economics of fast breeder reactors. An algebraic background is presented which represents the various views expressed by different nations regarding the cost of fast breeder reactors and their associated fuel cycle services, the timescale by which they might be available, and the simultaneous variations in the price of uranium. Actual presentations made by individual countries in recent discussions serve to verify the general nature of this present discussion. It is assumed that if nuclear power is to make a long term contribution to the needs of the world, the introduction of fast breeder reactors is both essential and necessary

Review of fast reactor activities

Energy Technology Data Exchange (ETDEWEB)

Balz, W [Commission of the European Communities, Brussels (Belgium)

1978-07-01

The Commission of the European Communities continued its activities on the following lines: activities aimed at preparing for commercialization of fast breeder reactors which are essentially performed in the frame of Fast Reactor Coordinating Committee (FRCC); the execution of its own research program in the Joint Research Center. The report covers activities of the FRCC, of the Safety Working Group (SWG), the Whole Core Accident Code (WAC) subgroup, Containment (CONT) subgroup, Codes and Standards Working Group (CSWG). Research and development activities are concerned with LMFBR safety, subassembly thermal hydraulics, fuel-coolant interactions, post-accident heat removal, dynamic load response, safety related material properties, utilization limits of fast breeder fuels, plutonium and actinide aspects of nuclear fuel cycle.

Review of fast reactor activities

International Nuclear Information System (INIS)

Balz, W.

1978-01-01

The Commission of the European Communities continued its activities on the following lines: activities aimed at preparing for commercialization of fast breeder reactors which are essentially performed in the frame of Fast Reactor Coordinating Committee (FRCC); the execution of its own research program in the Joint Research Center. The report covers activities of the FRCC, of the Safety Working Group (SWG), the Whole Core Accident Code (WAC) subgroup, Containment (CONT) subgroup, Codes and Standards Working Group (CSWG). Research and development activities are concerned with LMFBR safety, subassembly thermal hydraulics, fuel-coolant interactions, post-accident heat removal, dynamic load response, safety related material properties, utilization limits of fast breeder fuels, plutonium and actinide aspects of nuclear fuel cycle

Weapons-grade plutonium dispositioning. Volume 4

International Nuclear Information System (INIS)

Sterbentz, J.W.; Olsen, C.S.; Sinha, U.P.

1993-06-01

This study is in response to a request by the Reactor Panel Subcommittee of the National Academy of Sciences (NAS) Committee on International Security and Arms Control (CISAC) to evaluate the feasibility of using plutonium fuels (without uranium) for disposal in existing conventional or advanced light water reactor (LWR) designs and in low temperature/pressure LWR designs that might be developed for plutonium disposal. Three plutonium-based fuel forms (oxides, aluminum metallics, and carbides) are evaluated for neutronic performance, fabrication technology, and material and compatibility issues. For the carbides, only the fabrication technologies are addressed. Viable plutonium oxide fuels for conventional or advanced LWRs include plutonium-zirconium-calcium oxide (PuO 2 -ZrO 2 -CaO) with the addition of thorium oxide (ThO 2 ) or a burnable poison such as erbium oxide (Er 2 O 3 ) or europium oxide (Eu 2 O 3 ) to achieve acceptable neutronic performance. Thorium will breed fissile uranium that may be unacceptable from a proliferation standpoint. Fabrication of uranium and mixed uranium-plutonium oxide fuels is well established; however, fabrication of plutonium-based oxide fuels will require further development. Viable aluminum-plutonium metallic fuels for a low temperature/pressure LWR include plutonium aluminide in an aluminum matrix (PuAl 4 -Al) with the addition of a burnable poison such as erbium (Er) or europium (Eu). Fabrication of low-enriched plutonium in aluminum-plutonium metallic fuel rods was initially established 30 years ago and will require development to recapture and adapt the technology to meet current environmental and safety regulations. Fabrication of high-enriched uranium plate fuel by the picture-frame process is a well established process, but the use of plutonium would require the process to be upgraded in the United States to conform with current regulations and minimize the waste streams

Characterization of uranium- and plutonium-contaminated soils by electron microscopy

International Nuclear Information System (INIS)

Buck, E.C.; Dietz, N.L.; Fortner, J.A.; Bates, J.K.; Brown, N.R.

1995-01-01

Electron beam techniques have been used to characterize uranium-contaminated soils from the Fernald Site in Ohio, and also plutonium-bearing 'hot particles, from Johnston Island in the Pacific Ocean. By examining Fernald samples that had undergone chemical leaching it was possible to observe the effect the treatment had on specific uranium-bearing phases. The technique of Heap leaching, using carbonate solution, was found to be the most successful in removing uranium from Fernald soils, the Heap process allows aeration, which facilitates the oxidation of uraninite. However, another refractory uranium(IV) phase, uranium metaphosphate, was not removed or affected by any soil-washing process. Examination of ''hot particles'' from Johnston Island revealed that plutonium and uranium were present in 50--200 nm particles, both amorphous and crystalline, within a partially amorphous aluminum oxide matrix. The aluminum oxide is believed to have undergone a crystalline-to-amorphous transition caused by alpha-particle bombardment during the decay of the plutonium

Economic considerations of plutonium utilization in the nuclear power strategy of Finland

International Nuclear Information System (INIS)

Silvennoinen, P.; Tusa, E.; Routti, J.T.

1977-01-01

Based on the current and prospected share of nuclear power in the national energy supply strategy an optimal programme is developed for exploitation of plutonium in both light water and fast reactor systems. Assuming cost trends until and beyond the year 2000 for uranium, plutonium, uranium enrichment, fuel fabricaton and assessing the availability of plutonium from the domestic power plants and from abroad the nuclear construction programme is optimized economically in view of the estimated development in the investment costs of various plant types. Given the expected nuclear share of the energy procurement this sector is covered by the alternative production schemes, i.e. light water reactors with and without plutonium recycle and fast reactors. The plant sizes are allowed to be either 500 MWe or 1000 MWe. The installation dates are fixed manually with a minor flexibility of time but with all the three degrees of freedom in the plant types. Defining the objective function in terms of minimized revenue requirement in plant amortization and operation the generated scenarios are screened off and they finally converge to the optimal policy of nuclear power construction up to the year 2000. Special attention is placed on the constraints which eliminate excessive proliferation of reactor types. This is mainly implemented by the criterion of increasing the domestic share in the investments. The established technology is associated with a larger share of the Finnish manufacturing and the introduction of new fuel or reactor type is taken to correspond to a reduced domestic investment share. The results yield the time schedule and installed capacity of the three different production means. Due to the uncertainties prevailing in the forecasts sensitivity studies are performed as functions of the major economic parameters and their temporal development

A status report on the integral fast reactor fuels and safety program

International Nuclear Information System (INIS)

Pedersen, D.R.; Seidel, B.R.

1990-01-01

The integral fast reactor (IFR) is an advanced liquid-metal-cooled reactor (ALMR) concept being developed at Argonne National Laboratory. The IFR program is specifically responsible for the irradiation performance, advanced core design, safety analysis, and development of the fuel cycle for the US Department of Energy's ALMR program. The basic elements of the IFR concept are (a) metallic fuel, (b) liquid-sodium cooling, (c) modular, pool-type reactor configuration, (d) an integral fuel cycle based upon pyrometallurgical processing. The most significant safety aspects of the IFR program result from its unique fuel design, a ternary alloy of uranium, plutonium, and zirconium. This fuel is based on experience gained through > 25 yr operation of the Experimental Breeder Reactor II (EBR-II) with a uranium alloy metallic fuel. The ultimate criteria for fuel pin design is the overall integrity at the target burnup. The probability of core meltdown is remote; however, a theoretical possibility of core meltdown remains. The next major step in the IFR development program will be a full-scale pyroprocessing demonstration to be carried out in conjunction with EBR-II. The IFR fuel cycle closure based on pyroprocessing will also have a dramatic impact on waste management options and on actinide recycling

Uranium and plutonium distribution in unirradiated mixed oxide fuel from industrial fabrication

International Nuclear Information System (INIS)

Hanus, D.; Kleykamp, H.

1982-01-01

Different process variants developed in the last few years by the firm ALKEM to manufacture FBR and LWR mixed oxide fuel are given. The uranium and plutonium distribution is determined on the pellets manufactured with the help of the electron beam microprobe. The stepwise improvement of the uranium-plutonium homogeneity in the short-term developed granulate variants and in the long-term developed new processes are illustrated starting with early standard processes for FBR fuel. An almost uniform uranium-plutonium distribution could be achieved for the long-term developed new processes (OKOM, AuPuC). The uranium-plutonium homogeneity are quantified in the pellets manufactured according to the considered process variants with a newly defined quality number. (orig.)

Advancing liquid metal reactor technology with nitride fuels

International Nuclear Information System (INIS)

Lyon, W.F.; Baker, R.B.; Leggett, R.D.; Matthews, R.B.

1991-08-01

A review of the use of nitride fuels in liquid metal fast reactors is presented. Past studies indicate that both uranium nitride and uranium/plutonium nitride possess characteristics that may offer enhanced performance, particularly in the area of passive safety. To further quantify these effects, the analysis of a mixed-nitride fuel system utilizing the geometry and power level of the US Advanced Liquid Metal Reactor as a reference is described. 18 refs., 2 figs., 2 tabs

Transmutation of americium in critical reactors

International Nuclear Information System (INIS)

Wallenius, J.

2005-01-01

Already in 1974, a Los Alamos report suggested that the recycling of higher actinides would be detrimental for the safety of critical reactors. Later investigations confirmed this understanding, and stringent limits on the fraction of minor actinides allowed to be present in the fuel of fast neutron reactors were established. In recent years, and in particular in connection with the generation IV initiative, it has been advocated that recycling of americium in critical reactors is not only feasible, but also a recommendable approach. In the present contribution, it is shown, to the contrary, that introduction of americium into reactors with uranium based fuels deteriorates the safety margin of these reactors to a degree that will not allow consumption of the americium sources present in any economically competitive nuclear fuel cycle. Further, it is shown that uranium and thorium free cores with plutonium based fuels may be designed, that features excellent safety characteristics, as long as americium is not present in the feed. Hence, a closed fuel cycle is suggested, that consists of commercial power production in light water reactors, plutonium burning in uranium and thorium free fast neutron critical reactors, and higher actinide consumption in accelerator driven systems with inert matrix fuel. It is argued that such a fuel cycle (being a refinement of the Double Strata fuel cycle proposed by JAERI and further developed by M. Salvatores) provides a minimum cost penalty for implementing P and T under realistic boundary conditions. (author)

Plans and equipment for criticality measurements on plutonium-uranium nitrate solutions

International Nuclear Information System (INIS)

Lloyd, R.C.; Clayton, E.D.; Durst, B.M.

1982-01-01

Data from critical experiments are required on the criticality of plutonium-uranium nitrate solutions to accurately establish criticality control limits for use in processing and handling of breeder type fuels. Since the fuel must be processed both safely and economically, it is necessary that criticality considerations be based on accurate experimental data. Previous experiments have been reported on plutonium-uranium solutions with Pu weight ratios extending up to some 38 wt %. No data have been presented, however, for plutonium-uranium nitrate solutions beyond this Pu weight ratio. The current research emphasis is on the procurement of criticality data for plutonium-uranium mixtures up to 60 wt % Pu that will serve as the basis for handling criticality problems subsequently encountered in the development of technology for the breeder community. Such data also will provide necessary benchmarks for data testing and analysis on integral criticality experiments for verification of the analytical techniques used in support of criticality control. Experiments are currently being performed with plutonium-uranium nitrate solutions in stainless steel cylindrical vessels and an expandable slab tank system. A schematic of the experimental systems is presented

Present status and problems of development of fast breeder reactors

International Nuclear Information System (INIS)

Ikeda, Hiroshi

1984-11-01

The development of FBRs in Japan now reached the stage to conclude on the development organization for a demonstration reactor positioning one step before a practical reactor. FBRs can be operated while converting uranium-238 existing in natural uranium by 99.3% to fissile plutonium-239, as the result, the nuclear fuel more than that consumed can be produced. However, there are various technical difficulties in FBRs, and the construction cost is estimated to be considerably higher as compared with that of LWRs. Also the plutonium obtained by reprocessing spent fuel is used for FBRs, accordingly, the development of FBRs is inseparable from the establishment of nuclear fuel cycle. In order to get rid of the burden of enormous development cost for FBRs, the trend of international joint development is conspicuous. The Superphenix with 1200 MWe output under construction centering around SERENA is expected to attain the criticality in the spring of 1985. For the development of a demonstration reactor, it is necessary to increase the role of private businesses, and the smooth transfer of know-how accumulated in Power Reactor and Nuclear Fuel Development Corp. to civilian side is an important problem. (Kako, I.)

Gastrointestinal absorption and retention of plutonium and uranium in the baboon

International Nuclear Information System (INIS)

Larsen, R.P.; Bhattacharyya, M.H.; Oldham, R.D.; Moretti, E.S.; Cohen, N.

1984-01-01

Individual isotopes of plutonium and uranium were administered both intragastrically and intravenously to a baboon. Samples of urine, faces, blood, and tissues were taken and are now being analyzed. Preliminary results indicate that the fractional absorptions of plutonium and uranium were 1 x 10 -3 and 1 x 10 -2 , respectively, and their retentions about one month later were about 20% and 10%, respectively, of the amounts absorbed. The fractional retentions of the intravenously injected plutonium and uranium at that time were 0.90 and 0.07. 13 references, 1 figure, 3 tables

Reprocessing fuel from the Southwest Experimental Fast Oxide Reactor at the Savannah River Plant

International Nuclear Information System (INIS)

Gray, L.W.; Campbell, T.G.

1985-11-01

The irradiated fuel, reject fuel tubes, and fuel fabrication scrap from the Southwest Experimental Fast Oxide Reactor (SEFOR) were transferred to the Savannah River Plant (SRP) for uranium and plutonium recovery. The unirradiated material was declad and dissolved at SRP; dissolution was accomplished in concentrated nitric acid without the addition of fluoride. The irradiated fuel was declad at Atomics International and repacked in aluminum. The fuel and aluminum cans were dissolved at SRP using nitric acid catalyzed by mercuric nitrate. As this fuel was dissolved in nongeometrically favorable tanks, boron was used as a soluble neutron poison

Use of plutonium for power production

International Nuclear Information System (INIS)

1965-01-01

The panel reviewed available information on various aspects of plutonium utilization, such as physics of plutonium, technology of plutonium fuels in thermal and fast reactors, behaviour of plutonium fuel under reactor irradiation, technological and economic aspects of plutonium fuel cycle. Refs, figs and tabs

Pyro-electrochemical reprocessing of irradiated MOX fast reactor fuel, testing of the reprocessing process with direct MOX fuel production

Energy Technology Data Exchange (ETDEWEB)

Kormilitzyn, M.V.; Vavilov, S.K.; Bychkov, A.V.; Skiba, O.V.; Chistyakov, V.M.; Tselichshev, I.V

2000-07-01

One of the advanced technologies for fast reactor fuel recycle is pyro-electrochemical molten salt technology. In 1998 we began to study the next phase of the irradiated oxide fuel reprocessing new process MOX {yields} MOX. This process involves the following steps: - Dissolution of irradiated fuel in molten alkaline metal chlorides, - Purification of melt from fission products that are co-deposited with uranium and plutonium oxides, - Electrochemical co-deposition of uranium and plutonium oxides under the controlled cathode potential, - Production of granulated MOX (crushing,salt separation and sizing), and - Purification of melt from fission products by phosphate precipitation. In 1998 a series of experiments were prepared and carried out in order to validate this process. It was shown that the proposed reprocessing flowsheet of irradiated MOX fuel verified the feasibility of its decontamination from most of its fission products (rare earths, cesium) and minor-actinides (americium, curium)

Pyro-electrochemical reprocessing of irradiated MOX fast reactor fuel, testing of the reprocessing process with direct MOX fuel production

International Nuclear Information System (INIS)

Kormilitzyn, M.V.; Vavilov, S.K.; Bychkov, A.V.; Skiba, O.V.; Chistyakov, V.M.; Tselichshev, I.V.

2000-01-01

One of the advanced technologies for fast reactor fuel recycle is pyro-electrochemical molten salt technology. In 1998 we began to study the next phase of the irradiated oxide fuel reprocessing new process MOX → MOX. This process involves the following steps: - Dissolution of irradiated fuel in molten alkaline metal chlorides, - Purification of melt from fission products that are co-deposited with uranium and plutonium oxides, - Electrochemical co-deposition of uranium and plutonium oxides under the controlled cathode potential, - Production of granulated MOX (crushing,salt separation and sizing), and - Purification of melt from fission products by phosphate precipitation. In 1998 a series of experiments were prepared and carried out in order to validate this process. It was shown that the proposed reprocessing flowsheet of irradiated MOX fuel verified the feasibility of its decontamination from most of its fission products (rare earths, cesium) and minor-actinides (americium, curium)

A comparison of nuclear power systems for Brazil using plutonium and binary cycles

International Nuclear Information System (INIS)

Ishiguro, Y.; Fernandes, J.E.

1985-01-01

Nuclear power systems based on plutonium cycle and binary cycle are compared taking into account natural uranium demand and reactor combination. The systems start with PWR type reactors (U5/U8) and change to systems composed exclusively of FBR type reactors or PWR-FBR symbiotic systems. Four loading modes are considered for the PWR and two for the FBR. The FBR is either a LMFBR loaded with PU/U or a LMFBR loaded the binary way. A linear and a non-linear capacity growth and two different criteria for the FBR introduction are considered. The results show that a 100 GWe permanent system can be established in 50 years in all cases, based on 300000 t of natural uranium and in case of delay in the FBR introduction and if a thermal-fast symbiotic system is chosen, a binary cycle could be more advantageous than a plutonium cycle. (F.E.) [pt

Determination of uranium and plutonium in urine of people working with regenerated uranium

International Nuclear Information System (INIS)

Golutvina, M.M.; Ryzhova, E.A.

1987-01-01

Method of determining uranium and plutonium content in urine with their combined presence up to α-activity ratio Pu:U=1:100 is developed. The method is based on extraction chromatographic separation of nuclides using trimethyloctylammonium nitrate and their subsequent α-spectrometric determination. The coefficient of plutonium purification from uranium makes up 750. Chemical yield of Pu is 72±6%, U-76±8%. The method sensitivity is 0.2 decompositions per minute for a sample

Cyclopentadienyl uranium, neptunium and plutonium chemistry

International Nuclear Information System (INIS)

Plews, M.J.

1985-01-01

The thesis presents the preparation and characterisation of a number of mono, bis and tris(cyclopentadienyl) complexes of uranium(IV), neptunium(IV) and plutonium(IV). The work of previous studies on mono(cyclopentadienyl) thorium and uranium complexes has been extended, and a range of isostructural neptunium species isolated. Their mode of formation and stability in tetrahydrofuran and acetonitrile solutions was investigated. (author)

DOE plutonium disposition study: Analysis of existing ABB-CE Light Water Reactors for the disposition of weapons-grade plutonium

International Nuclear Information System (INIS)

1994-01-01

Core reactivity and basic fuel management calculations were conducted on the selected reactors (with emphasis on the System 80 units as being the most desirable choice). Methods used were identical to those reported in the Evolutionary Reactor Report. From these calculations, the basic mission capability was assessed. The selected reactors were studied for modification, such as the addition of control rod nozzles to increase rod worth, and internals and control system modifications that might also be needed. Other system modifications studied included the use of enriched boric acid as soluble poison, and examination of the fuel pool capacities. The basic geometry and mechanical characteristics, materials and fabrication techniques of the fuel assemblies for the selected existing reactors are the same as for System 80+. There will be some differences in plutonium loading, according to the ability of the reactors to load MOX fuel. These differences are not expected to affect licensability or EPA requirements. Therefore, the fuel technology and fuel qualification sections provided in the Evolutionary Reactor Report apply to the existing reactors. An additional factor, in that the existing reactor availability presupposes the use of that reactor for the irradiation of Lead Test Assemblies, is discussed. The reactor operating and facility licenses for the operating plants were reviewed. Licensing strategies for each selected reactor were identified. The spent fuel pool for the selected reactors (Palo Verde) was reviewed for capacity and upgrade requirements. Reactor waste streams were identified and assessed in comparison to uranium fuel operations. Cost assessments and schedules for converting to plutonium disposition were estimated for some of the major modification items. Economic factors (incremental costs associated with using weapons plutonium) were listed and where possible under the scope of work, estimates were made

Advanced plutonium management in PWR - complementarity of thorium and uranium cycles

International Nuclear Information System (INIS)

Ernoult, Marc

2014-01-01

In order to study the possibility of advanced management of plutonium in existing reactors, 8 strategies for plutonium multi-recycling in PWRs are studied. Following equilibrium studies, it was shown that, by using homogeneous assemblies, the use of thorium cannot reduce the plutonium inventory of equilibrium cycle or production of americium. By distributing the different fuel types within the same assembly, some thoriated strategies allow however lower inventories and lower production americium best strategies using only the uranium cycle. However, in all cases, low fuel conversion theories in PWRs makes it impossible to lower resource consumption more than a few percent compared to strategies without thorium. To study the transition, active participation in development of the scenario code CLASS has been taken. It led to the two simulation scenarios among those studied in equilibrium with CLASS. These simulations have shown discrepancies with previously simulated scenarios. The major causes of these differences were identified and quantified. (author)

Interim report of the subcommittee on putting fast breeder reactors in practical use

International Nuclear Information System (INIS)

1983-01-01

Light water reactors are expected to be the main power reactors in Japan for considerably long period hereafter, however, the basic policy of long term energy utilization is to use the plutonium and depleted uranium recovered by the reprocessing of spent fuel for fast breeder reactors, in view of the effective use of energy resources and the energy security. At present, the experimental FBR ''Joyo'' is in operation, and the preparation work was started for the prototype FBR ''Monju'', aiming at the criticality at the end of fiscal 1990. In the discussion, it was confirmed that for the practical use of FBRs, the improvement of their economy is the most important. But the construction cost for the Monju and the type of the demonstration FBR are not yet decided, and there are many uncertain elements. The demand and supply of uranium and the prospect of FBR development, the appropriate way of FBR development in Japan, the trend of FBR development in Japan and foreign countries, the evaluation of the economy of FBRs and the time of putting in practical use, the schedule of FBR development, the cost reduction in FBRs, the fuel cycle and others are reported. (Kako, I.)

Phenomenology of uranium-plutonium homogenization in nuclear fuels

International Nuclear Information System (INIS)

Marin, J.M.

1988-01-01

The uranium and plutonium cations distribution in mixed oxide fuels (U 1-y Pu y )O 2 with y ≤ 0.1 has been studied in laboratory with industrial fabrication methods. Our experiences has showed a slow cations migration. In the substoichiometry (UPu)O 2-x the diffusion is in connection with the plutonium valence which is an indicator of the oxidoreduction state of the crystal lattice. The plutonium valence is in connection with the oxygen ion deficit in order to compensate the electrical charge. The oxygen ratio of the solid depends of the oxygen partial pressure prevailing at the time of product elaboration but it can be modified by impurities. These impurities permit to increase or decrease the fuel characteristics and performances. An homogeneity analysis methodology is proposed, its objective is to classify the mixed oxide fuels according to the uranium and plutonium ions distribution [fr

Review of Sodium and Plutonium related Technical Standards in Trans-Uranium Fuel Fabrication Facilities

Energy Technology Data Exchange (ETDEWEB)

Jang, Misuk; Jeon, Jong Seon; Kang, Hyun Sik; Kim, Seoung Rae [NESS, Daejeon (Korea, Republic of)

2016-10-15

In this paper, we would introduce and review technical standards related to sodium fire and plutonium criticality safety. This paper may be helpful to identify considerations in the development of equipment, standards, and etc., to meet the safety requirements in the design, construction and operating of TFFF, KAPF and SFR. The feasibility and conceptual designs are being examined on related facilities, for example, TRU Fuel Fabrication Facilities (TFFF), Korea Advanced Pyro-process Facility (KAPF), and Sodium Cooled Fast Reactor (SFR), in Korea. However, the safety concerns of these facilities have been controversial in part because of the Sodium fire accident and Plutonium related radiation safety caused by transport and handling accident. Thus, many researches have been performed to ensure safety and various documents including safety requirements have been developed. In separating and reducing the long-lived radioactive transuranic(TRU) in the spent nuclear fuel, reusing as the potential energy of uranium fuel resources and reducing the high level wastes, TFFF would be receiving the attention of many people. Thus, people would wonder whether compliance with technical standards that ensures safety. For new facility design, one of the important tasks is to review of technical standards, especially for sodium and Plutonium because of water related highly reactive characteristics and criticality hazard respectively. We have introduced and reviewed two important technical standards for TFFF, which are sodium fire and plutonium criticality safety, in this paper. This paper would provide a brief guidance, about how to start and what is important, to people who are responsible for the initial design to operation of TFFF.

Review of Sodium and Plutonium related Technical Standards in Trans-Uranium Fuel Fabrication Facilities

International Nuclear Information System (INIS)

Jang, Misuk; Jeon, Jong Seon; Kang, Hyun Sik; Kim, Seoung Rae

2016-01-01

In this paper, we would introduce and review technical standards related to sodium fire and plutonium criticality safety. This paper may be helpful to identify considerations in the development of equipment, standards, and etc., to meet the safety requirements in the design, construction and operating of TFFF, KAPF and SFR. The feasibility and conceptual designs are being examined on related facilities, for example, TRU Fuel Fabrication Facilities (TFFF), Korea Advanced Pyro-process Facility (KAPF), and Sodium Cooled Fast Reactor (SFR), in Korea. However, the safety concerns of these facilities have been controversial in part because of the Sodium fire accident and Plutonium related radiation safety caused by transport and handling accident. Thus, many researches have been performed to ensure safety and various documents including safety requirements have been developed. In separating and reducing the long-lived radioactive transuranic(TRU) in the spent nuclear fuel, reusing as the potential energy of uranium fuel resources and reducing the high level wastes, TFFF would be receiving the attention of many people. Thus, people would wonder whether compliance with technical standards that ensures safety. For new facility design, one of the important tasks is to review of technical standards, especially for sodium and Plutonium because of water related highly reactive characteristics and criticality hazard respectively. We have introduced and reviewed two important technical standards for TFFF, which are sodium fire and plutonium criticality safety, in this paper. This paper would provide a brief guidance, about how to start and what is important, to people who are responsible for the initial design to operation of TFFF

Method of stripping plutonium from tributyl phosphate solution which contains dibutyl phosphate-plutonium stable complexes

International Nuclear Information System (INIS)

Ochsenfeld, W.; Schmieder, H.

1976-01-01

Fast breeder fuel elements which have been highly burnt-up are reprocessed by extracting uranium and plutonium into an organic solution containing tributyl phosphate. The tributyl phosphate degenerates at least partially into dibutyl phosphate and monobutyl phosphate, which form stable complexes with tetravalent plutonium in the organic solution. This tetravalent plutonium is released from its complexed state and stripped into aqueous phase by contacting the organic solution with an aqueous phase containing tetravalent uranium. 6 claims, 1 drawing figure

Development of a new measurement method for fast breeder reactor fuel burnup using a shielded ion microprobe analyzer

International Nuclear Information System (INIS)

Mizuno, M.; Enokido, Y.; Itaki, T.; Kono, K.; Unno, I.; Yamanouchi, S.

1985-01-01

A new method of burnup measurement using a shielded ion microprobe analyzer (SIMA) has been developed. The method is based on the isotope analysis of uranium, plutonium, and fission products in irradiated mixed oxide fuel by means of secondary ion mass spectrometry (SIMS). Fourteen samples irradiated in the Japanese experimental fast reactor JOYO were examined. The maximum local burnup of JOYO MK-I core fuels was about5.1 at. %. The axial burnup distribution of the fuel pin was in good agreement with that of the sibling pin in the same subassembly, measured by surface ionization mass spectrometry, which requires the chemical separation of fission products and heavy metals. The new method facilitates the rapid and accurate measurement of fast breeder reactor fuel burnup without human radiation exposure during sample preparation and analysis

Plutonium Plant, Trombay

International Nuclear Information System (INIS)

Yadav, J.S.; Agarwal, K.

2017-01-01

The journey of Indian nuclear fuel reprocessing started with the commissioning of Plutonium Plant (PP) at Trombay on 22"n"d January, 1965 with an aim to reprocess the spent fuel from research reactor CIRUS. The basic process chosen for the plant was Plutonium Uranium Reduction EXtraction (PUREX) process. In seventies, the plant was subjected to major design modifications and replacement of hardware, which later met the additional demand from research reactor DHRUVA. The augmented plutonium plant has been operating since 1983. Experience gained from this plant was very much helpful to design future reprocessing plant in the country

METHOD OF SEPARATING URANIUM VALUES, PLUTONIUM VALUES AND FISSION PRODUCTS BY CHLORINATION

Science.gov (United States)

Brown, H.S.; Seaborg, G.T.

1959-02-24

The separation of plutonium and uranium from each other and from other substances is described. In general, the method comprises the steps of contacting the uranium with chlorine in the presence of a holdback material selected from the group consisting of lanthanum oxide and thorium oxide to form a uranium chloride higher than uranium tetrachloride, and thereafter heating the uranium chloride thus formed to a temperature at which the uranium chloride is volatilized off but below the volatilizalion temperature of plutonium chloride.

The differential radiological impact of plutonium recycle in the light-water reactor fuel cycle: effluent discharges during normal operation

International Nuclear Information System (INIS)

Bouville, A.; Guetat, P.; Jones, J.A.; Kelly, G.N.; Legrand, J.; White, I.F.

1980-01-01

The radiological impact of a light-water reactor fuel cycle utilizing enriched uranium fuel may be altered by the recycle of plutonium. Differences in impact may arise during various operations in the fuel cycle: those which arise from effluents discharged during normal operation of the various installations comprising the fuel cycle are evaluated in this study. The differential radiological impact on the population of the European Communities (EC) of effluents discharged during the recycling of 10 tonnes of fissile plutonium metal is evaluated. The contributions from each stage of the fuel cycle, i.e. fuel fabrication, reactor operation and fuel reprocessing and conversion, are identified. Separate consideration is given to airborne and liquid effluents and account is taken of a wide range of environmental conditions, representative of the EC, in estimating the radiological impact. The recycle of plutonium is estimated to result in a reduction in the radiological impact from effluents of about 30% of that when using enriched uranium fuel

Optimisation of parameters for co-precipitation of uranium and plutonium - results of simulation studies

International Nuclear Information System (INIS)

Pandey, N.K.; Velvandan, P.V.; Murugesan, S.; Ahmed, M.K.; Koganti, S.B.

1999-01-01

Preparation of plutonium oxide from plutonium nitrate solution generally proceeds via oxalate precipitation route. In a nuclear fuel reprocessing scheme this step succeeds the partitioning step (separation of uranium and plutonium). Results of present studies confirm that it is possible to avoid partitioning step and recover plutonium and uranium as co-precipitated product. This also helps in minimising the risk of proliferation of fissile material. In this procedure, the solubility of uranium oxalate in nitric acid is effectively used. Co-precipitation parameters are optimised with simulated solutions of uranium nitrate and thorium nitrate (in place of plutonium). On the basis of obtained results a reconversion flow-sheet is designed and reported here. (author)

Ceramics as nuclear reactor fuels

International Nuclear Information System (INIS)

Reeve, K.D.

1975-01-01

Ceramics are widely accepted as nuclear reactor fuel materials, for both metal clad ceramic and all-ceramic fuel designs. Metal clad UO 2 is used commercially in large tonnages in five different power reactor designs. UO 2 pellets are made by familiar ceramic techniques but in a reactor they undergo complex thermal and chemical changes which must be thoroughly understood. Metal clad uranium-plutonium dioxide is used in present day fast breeder reactors, but may eventually be replaced by uranium-plutonium carbide or nitride. All-ceramic fuels, which are necessary for reactors operating above about 750 0 C, must incorporate one or more fission product retentive ceramic coatings. BeO-coated BeO matrix dispersion fuels and silicate glaze coated UO 2 -SiO 2 have been studied for specialised applications, but the only commercial high temperature fuel is based on graphite in which small fuel particles, each coated with vapour deposited carbon and silicon carbide, are dispersed. Ceramists have much to contribute to many aspects of fuel science and technology. (author)

Coolant-fuel interaction in Sodium-cooled Fast Reactors: Structural investigations of The Na-An-O (An = U, Np, Pu) systems

International Nuclear Information System (INIS)

Smith, A.L.; Raison, P.E.; Bykov, D.M.; Konings, R.J.; Caciuffo, R.; Cheetham, A.K.

2014-01-01

Nuclear energy has the potential to provide Europe with a secure and sustainable electricity supply at a competitive price and to make a significant contribution to the reduction of greenhouse gases emissions. The interest for Sodium-cooled-Fast-spectrum Reactors (SFRs), when compared to Pressurized Water Reactors (PWRs), lies in their more efficient management of plutonium and other actinides as well as their ability to use almost all of the energy in the natural uranium versus 1% utilized in thermal spectrum systems. The high fuel efficiency of fast reactors could greatly dampen concerns about fuel supply. But these reactors have also several drawbacks when compared to PWRs (i.e sodium fire, Na reaction with O2 and H2O, interaction of sodium with oxide fuels). Their development at an industrial scale needs therefore an exhaustive safety assessment that comprises both experimental work and development of sophisticated modelling tools able to describe the reactor behaviour in normal or incidental conditions

Improved locations of reactivity devices in future CANDU reactors fuelled with natural uranium or enriched fuels

International Nuclear Information System (INIS)

Boczar, P.G.; Van Dyk, M.T.

1987-02-01

A new configuration of reactivity devices is proposed for future CANDU reactors which improves the core characteristics with enriched fuels, while still allowing the use of natural uranium fuel. Physics calculations for this new configuration are presented for four fuel types: natural uranium, mixed plutonium - uranium oxide (MOX) having a burnup of 21 MWd/kg, and slightly enriched uranium (SEU) having burnups of either 21 or 31 MWd/kg

Total decay heat estimates in a proto-type fast reactor

International Nuclear Information System (INIS)

Sridharan, M.S.

2003-01-01

Full text: In this paper, total decay heat values generated in a proto-type fast reactor are estimated. These values are compared with those of certain fast reactors. Simple analytical fits are also obtained for these values which can serve as a handy and convenient tool in engineering design studies. These decay heat values taken as their ratio to the nominal operating power are, in general, applicable to any typical plutonium based fast reactor and are useful inputs to the design of decay-heat removal systems

Metallographic preparation of sintered oxides, carbides and nitrides of uranium and plutonium

International Nuclear Information System (INIS)

Martin, A.; Arles, L.

1967-12-01

We describe the methods of polishing, attack and coloring used at the section of plutonium base ceramics studies. These methods have stood the test of experience on the uranium and plutonium carbides, nitrides and carbonitrides as well on the mixed uranium and plutonium oxides. These methods have been particularly adapted to fit to the low dense and sintered samples [fr

Liquid-metal fast-breeder reactors: Preliminary safety and environmental information document. Volume VI

International Nuclear Information System (INIS)

1980-01-01

Information is presented concerning LMFBR design characteristics; uranium-plutonium/uranium recycle homogeneous core; uranium-plutonium/uranium spiked recycle heterogeneous core; uranium-plutonium/uranium spiked recycle homogeneous core; uranium-plutonium/thorium spiked recycle heterogeneous core; uranium-plutonium/thorium spiked recycle homogeneous core; thorium-plutonium/thorium spiked recycle homogeneous core; denatured uranium-233/thorium cycle homogeneous core; safety consideration for the LMFBR; and environmental considerations

Water Solubility of Plutonium and Uranium Compounds and Residues at TA-55

International Nuclear Information System (INIS)

Reilly, Sean Douglas; Smith, Paul Herrick; Jarvinen, Gordon D.; Prochnow, David Adrian; Schulte, Louis D.; DeBurgomaster, Paul Christopher; Fife, Keith William; Rubin, Jim; Worl, Laura Ann

2016-01-01

Understanding the water solubility of plutonium and uranium compounds and residues at TA-55 is necessary to provide a technical basis for appropriate criticality safety, safety basis and accountability controls. Individual compound solubility was determined using published solubility data and solution thermodynamic modeling. Residue solubility was estimated using a combination of published technical reports and process knowledge of constituent compounds. The scope of materials considered includes all compounds and residues at TA-55 as of March 2016 that contain Pu-239 or U-235 where any single item in the facility has more than 500 g of nuclear material. This analysis indicates that the following materials are not appreciably soluble in water: plutonium dioxide (IDC=C21), plutonium phosphate (IDC=C66), plutonium tetrafluoride (IDC=C80), plutonium filter residue (IDC=R26), plutonium hydroxide precipitate (IDC=R41), plutonium DOR salt (IDC=R42), plutonium incinerator ash (IDC=R47), uranium carbide (IDC=C13), uranium dioxide (IDC=C21), U 3 O 8 (IDC=C88), and uranium filter residue (IDC=R26). This analysis also indicates that the following materials are soluble in water: plutonium chloride (IDC=C19) and uranium nitrate (IDC=C52). Equilibrium calculations suggest that PuOCl is water soluble under certain conditions, but some plutonium processing reports indicate that it is insoluble when present in electrorefining residues (R65). Plutonium molten salt extraction residues (IDC=R83) contain significant quantities of PuCl 3 , and are expected to be soluble in water. The solubility of the following plutonium residues is indeterminate due to conflicting reports, insufficient process knowledge or process-dependent composition: calcium salt (IDC=R09), electrorefining salt (IDC=R65), salt (IDC=R71), silica (IDC=R73) and sweepings/screenings (IDC=R78). Solution thermodynamic modeling also indicates that fire suppression water buffered with a commercially-available phosphate

Water Solubility of Plutonium and Uranium Compounds and Residues at TA-55

Energy Technology Data Exchange (ETDEWEB)

Reilly, Sean Douglas [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Smith, Paul Herrick [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Jarvinen, Gordon D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Prochnow, David Adrian [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Schulte, Louis D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; DeBurgomaster, Paul Christopher [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Fife, Keith William [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Rubin, Jim [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Worl, Laura Ann [Los Alamos National Lab. (LANL), Los Alamos, NM (United States

2016-06-13

Understanding the water solubility of plutonium and uranium compounds and residues at TA-55 is necessary to provide a technical basis for appropriate criticality safety, safety basis and accountability controls. Individual compound solubility was determined using published solubility data and solution thermodynamic modeling. Residue solubility was estimated using a combination of published technical reports and process knowledge of constituent compounds. The scope of materials considered includes all compounds and residues at TA-55 as of March 2016 that contain Pu-239 or U-235 where any single item in the facility has more than 500 g of nuclear material. This analysis indicates that the following materials are not appreciably soluble in water: plutonium dioxide (IDC=C21), plutonium phosphate (IDC=C66), plutonium tetrafluoride (IDC=C80), plutonium filter residue (IDC=R26), plutonium hydroxide precipitate (IDC=R41), plutonium DOR salt (IDC=R42), plutonium incinerator ash (IDC=R47), uranium carbide (IDC=C13), uranium dioxide (IDC=C21), U₃O₈ (IDC=C88), and uranium filter residue (IDC=R26). This analysis also indicates that the following materials are soluble in water: plutonium chloride (IDC=C19) and uranium nitrate (IDC=C52). Equilibrium calculations suggest that PuOCl is water soluble under certain conditions, but some plutonium processing reports indicate that it is insoluble when present in electrorefining residues (R65). Plutonium molten salt extraction residues (IDC=R83) contain significant quantities of PuCl₃, and are expected to be soluble in water. The solubility of the following plutonium residues is indeterminate due to conflicting reports, insufficient process knowledge or process-dependent composition: calcium salt (IDC=R09), electrorefining salt (IDC=R65), salt (IDC=R71), silica (IDC=R73) and sweepings/screenings (IDC=R78). Solution thermodynamic modeling also indicates that fire suppression water buffered with a

Some safety studies for conceptual fusion--fission hybrid reactors. Final report

International Nuclear Information System (INIS)

Kastenberg, W.E.; Okrent, D.

1978-07-01

The objective of this study was to make a preliminary examination of some potential safety questions for conceptual fusion-fission hybrid reactors. The study and subsequent analysis was largely based upon reference to one design, a conceptual mirror fusion-fission reactor, operating on the deuterium-tritium plasma fusion fuel cycle and the uranium-plutonium fission fuel cycle. The blanket is a fast-spectrum, uranium carbide, helium cooled, subcritical reactor, optimized for the production of fissile fuel. An attempt was made to generalize the results wherever possible

Actinide transmutation using inert matrix fuels versus recycle in a low conversion fast burner reactor

Energy Technology Data Exchange (ETDEWEB)

Deinert, M.R.; Schneider, E.A.; Recktenwald, G.; Cady, K.B. [The Department of Mechanical Engineering, The University of Texas at Austin, 1 University Station, C2200, Austin, 78712 (United States)

2009-06-15

Reducing the disposal burden of the long lived radioisotopes that are contained within spent uranium oxide fuel is essential for ensuring the sustainability of nuclear power. Because of their non-fertile matrices, inert matrix fuels (IMFs) could allow light-water reactors to achieve a significant burn down of plutonium and minor actinides that are that are currently produced as a byproduct of operating light-water reactors. However, the extent to which this is possible is not yet fully understood. We consider a ZrO{sub 2} based IMF with a high transuranic loading and show that the neutron fluence (and the subsequent fuel residence time required to achieve it) present a practical limit for the achievable actinide burnup. The accumulation of transuranics in spent uranium oxide fuel is a major obstacle for the sustainability of nuclear power. While commercial light-water reactors (LWR's) produce these isotopes, they can be used to transmute them. At present, the only viable option for doing this is to partly fuel reactors with mixed oxide fuel (MOX) made using recycled plutonium. However, because of parasitic neutron capture in the uranium matrix of MOX, considerable plutonium and minor actinides are also bred as the fuel is burned. A better option is to entrain the recycled isotopes in a non-fertile matrix such as ZrO{sub 2}. Inert matrices such as these were originally envisioned for burning plutonium from dismantled nuclear weapons [1]. However, because they achieve a conversion ratio of zero, they have also been considered as a better alternative to MOX [2-6]. Plutonium and minor actinides dominate the long term heat and radiological outputs from spent nuclear fuel. Recent work has shown that that IMFs can be used to reduce these outputs by at least a factor of four, on a per unit of energy generated basis [6]. The degree of reduction is strongly dependent on IMF burnup. In principle, complete transmutation of the transuranics could be achieved though this

An investigation into the use of a fast breeder reactor to incinerate actinide waste from the U.K. nuclear power programme

International Nuclear Information System (INIS)

Harte, G.A.; Clarke, R.H.

1976-12-01

Preliminary investigations are described into the effect of actinide removal and incineration (i.e. re-irradiation in a high neutron flux) on the long term hazards of reprocessing wastes from a Magnox reactor and from a notional CFR operated on plutonium from a Magnox reactor and also from an AGR. The actinides neptunium, americium and curium extracted from these wastes would be amenable to incineration in a fast breeder reactor core with fluxes of the order of 10 16 ncm -2 s -1 . An incineration period of 35 years was found to achieve a reduction in hazard, for most cooling periods up to one million years. The reductions were 2 to 3 orders of magnitude for the Magnox wastes and 4 orders of magnitude for the waste from CFR fuelled with AGR-plutonium. The large reduction factors do not apply to the hazards of reprocessing wastes as a whole, however, since one actinide separation has been achieved the residual quantities of uranium and plutonium in the waste stream, assumed here to be 0.1% of the original fuel inventory of these elements, become dominant in determining the hazard. Shorter incineration periods may serve to reduce the hazards of the extracted transuranics below the levels determined by these residues. A discussion of the hazards associated with reprocessing wastes as compared to those associated with uranium mill tailings attempts to place the nuclear waste disposal problem in perspective. (author)

Automated spectrophotometer for plutonium and uranium determination

International Nuclear Information System (INIS)

Jackson, D.D.; Hodgkins, D.J.; Hollen, R.M.; Rein, J.E.

1975-09-01

The automated spectrophotometer described is the first in a planned series of automated instruments for determining plutonium and uranium in nuclear fuel cycle materials. It has a throughput rate of 5 min per sample and uses a highly specific method of analysis for these elements. The range of plutonium and uranium measured is 0.5 to 14 mg and 1 to 14 mg, respectively, in 0.5 ml or less of solution with an option to pre-evaporate larger volumes. The precision of the measurements is about 0.02 mg standard deviation over the range corresponding to about 2 rel percent at the 1-mg level and 0.2 rel percent at the 10-mg level. The method of analysis involves the extraction of tetrapropylammonium plutonyl and uranyl trinitrate complexes into 2-nitropropane and the measurement of the optical absorbances in the organic phase at unique peak wavelengths. Various aspects of the chemistry associated with the method are presented. The automated spectrophotometer features a turntable that rotates as many as 24 samples in tubes to a series of stations for the sequential chemical operations of reagent addition and phase mixing to effect extraction, and then to a station for the absorbance measurement. With this system, the complications of sample transfers and flow-through cells are avoided. The absorbance measurement system features highly stable interference filters and a microcomputer that controls the timing sequence and operation of the system components. Output is a paper tape printout of three numbers: a four-digit number proportional to the quantity of plutonium or uranium, a two-digit number that designates the position of the tube in the turntable, and a one-digit number that designates whether plutonium or uranium was determined. Details of the mechanical and electrical components of the instrument and of the hardware and software aspects of the computerized control system are provided

Kinetic study of the fluorination by fluorine of some uranium and plutonium compounds; Etude cinetique de la fluoration par le fluor de quelques composes de l'uranium et du plutonium

Energy Technology Data Exchange (ETDEWEB)

Vandenbussche, G [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

1964-12-15

The study of fluorination reactions of uranium and plutonium compounds with elementary fluorine, has been carried out using a thermogravimetric method. These reactions are heterogeneous ones, and of the following type: S(solid) + G{sub 1}(gas) - G{sub 2}(gas). The kinetics of these reactions correspond to a uniform attack of the entire surface of the sample. {alpha}: being the degree of completion of the reaction, k(rel): being the relative rate of penetration of the reaction interface, t: being the time, one have the relation: (1-{alpha}){sup 1/3} = 1 - k(rel)*t. The mechanism of the reaction varies according to the nature of the compound: 1) with uranium tetrafluoride and plutonium tetrafluoride, the reaction proceeds in a single step; 2) with uranium oxides, the reaction proceeds in two steps, uranium oxyfluoride being the intermediate compound; 3) with plutonium oxide, the reaction proceeds in two steps, plutonium tetrafluoride being the intermediate compound; and 4) with uranium trichloride, the mechanism is complex: chlorine trifluoride is formed. (author) [French] L'etude des reactions de fluoration par le fluor, de composes de l'uranium et du plutonium a ete faite par thermogravimetrie. Ce sont des reactions heterogenes du type: S(solide) + G{sub 1}(gaz) - G{sub 2}(gaz). La cinetique de ces reactions est celle correspondant a une attaque uniforme de toute la surface de l'echantillon. Si {alpha}: est le degre d'avancement de la reaction, k(rel): est la vitesse relative d'avancement d'un interface reactionnel, t: le temps. On a la relation: (1-{alpha}){sup 1/3} = 1-k(rel)*t. Le mecanisme de la reaction varie selon la nature du compose: 1) tetrafluorure d'uranium et tetrafluorure de plutonium, la reaction s'effectue en un seul stade; 2) Oxydes d'uranium: la reaction s'effectue en deux stades, l'oxyfluorure d'uranium est le compose intermediaire; 3) oxyde de plutonium, la reaction s'effectue en deux stades, la tetrafluorure de plutonium est le compose

Status of power reactor fuel reprocessing in India

International Nuclear Information System (INIS)

Kansra, V.P.

1999-01-01

Spent fuel reprocessing in India started with the commissioning of the Trombay Plutonium Plant in 1964. This plant was intended for processing spent fuel from the 40 MWth research reactor CIRUS and recovering plutonium required for the research and development activities of the Indian Atomic Energy programme. India's nuclear energy programme aims at the recycle of plutonium in view of the limited national resources of natural uranium and abundant quantities of thorium. This is based on the approach which aims at separating the plutonium from the power reactor spent fuel, use it in the fast reactors to breed 233 U and utilise the 233 U generated to sustain a virtually endless source of power through thorium utilisation. The separated plutonium is also being utilised to fabricate MOX fuel for use in thermal reactors. Spent fuel treatment and extracting plutonium from it makes economic sense and a necessity for the Indian nuclear power programme. This paper describes the status and trends in the Indian programme for the reprocessing of power reactor fuels. The extraction of plutonium can also be seen as a far more positive approach to long-term waste management. The closed cycle approach visualised and pursued by the pioneers in the field is now steadily moving India towards the goal of a sustainable source of power through nuclear energy. The experience in building, operating and refurbishing the reprocessing facilities for uranium and thorium has resulted in acquiring the technological capability for designing, constructing, operating and maintaining reprocessing plants to match India's growing nuclear power programme. (author)

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2009-01-01

The Director General has received a letter dated 16 July 2009 from the Permanent Mission of the Federal Republic of Germany to the IAEA in enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2008. 2. The Government of the Federal Republic of Germany has also made available a statement of its annual figures for holdings of civil high enriched uranium (HEU) as of 31 December 2008 [es

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2012-01-01

The Director General has received a note verbale dated 14 October 2010 from the Permanent Mission of the Federal Republic of Germany to the IAEA in enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2009. The Government of the Federal Republic of Germany has also made available a statement of its annual figures for holdings of civil high enriched uranium (HEU) as of 31 December 2009 [es

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2012-01-01

The Secretariat has received a note verbale dated 20 September 2012 from the Permanent Mission of the Federal Republic of Germany to the IAEA in the enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2011. The Government of the Federal Republic of Germany has also made available a statement of the estimated amounts of highly enriched uranium (HEU) as of 31 December 2011 [es

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of Highly Enriched Uranium

International Nuclear Information System (INIS)

2007-01-01

The Director General has received a Note Verbale dated 3 July 2007 from the Permanent Mission of the Federal Republic of Germany to the IAEA in the enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/549 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2006. The Government of the Federal Republic of Germany has also made available a statement of its annual figures for holdings of civil highly enriched uranium (HEU) as of 31 December 2006 [es

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2013-01-01

The Secretariat has received a note verbale dated 2 July 2013 from the Permanent Mission of the Federal Republic of Germany to the IAEA in the enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2012. The Government of the Federal Republic of Germany has also made available a statement of the estimated amounts of highly enriched uranium (HEU) as of 31 December 2012 [es

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2011-01-01

The Director General has received a note verbale dated 29 April 2011 from the Permanent Mission of the Federal Republic of Germany to the IAEA in enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2010. The Government of the Federal Republic of Germany has also made available a statement of its annual figures for holdings of civil high enriched uranium (HEU) as of 31 December 2010 [es

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2012-01-01

The Secretariat has received a note verbale dated 20 September 2012 from the Permanent Mission of the Federal Republic of Germany to the IAEA in the enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2011. The Government of the Federal Republic of Germany has also made available a statement of the estimated amounts of highly enriched uranium (HEU) as of 31 December 2011

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2011-01-01

The Director General has received a note verbale dated 14 October 2010 from the Permanent Mission of the Federal Republic of Germany to the IAEA in enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2009. The Government of the Federal Republic of Germany has also made available a statement of its annual figures for holdings of civil high enriched uranium (HEU) as of 31 December 2009

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2011-01-01

The Director General has received a note verbale dated 29 April 2011 from the Permanent Mission of the Federal Republic of Germany to the IAEA in enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2010. The Government of the Federal Republic of Germany has also made available a statement of its annual figures for holdings of civil high enriched uranium (HEU) as of 31 December 2010

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2009-01-01

The Director General has received a letter dated 16 July 2009 from the Permanent Mission of the Federal Republic of Germany to the IAEA in enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2008. 2. The Government of the Federal Republic of Germany has also made available a statement of its annual figures for holdings of civil high enriched uranium (HEU) as of 31 December 2008

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2013-01-01

The Secretariat has received a note verbale dated 2 July 2013 from the Permanent Mission of the Federal Republic of Germany to the IAEA in the enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2012. The Government of the Federal Republic of Germany has also made available a statement of the estimated amounts of highly enriched uranium (HEU) as of 31 December 2012

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of Highly Enriched Uranium

International Nuclear Information System (INIS)

2007-01-01

The Director General has received a Note Verbale dated 3 July 2007 from the Permanent Mission of the Federal Republic of Germany to the IAEA in the enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/549 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2006. The Government of the Federal Republic of Germany has also made available a statement of its annual figures for holdings of civil highly enriched uranium (HEU) as of 31 December 2006

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2011-01-01

The Director General has received a note verbale dated 29 April 2011 from the Permanent Mission of the Federal Republic of Germany to the IAEA in enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2010. The Government of the Federal Republic of Germany has also made available a statement of its annual figures for holdings of civil high enriched uranium (HEU) as of 31 December 2010 [fr

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2010-01-01

The Director General has received a note verbale dated 14 October 2010 from the Permanent Mission of the Federal Republic of Germany to the IAEA in enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2009. The Government of the Federal Republic of Germany has also made available a statement of its annual figures for holdings of civil high enriched uranium (HEU) as of 31 December 2009

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2013-01-01

The Secretariat has received a note verbale dated 2 July 2013 from the Permanent Mission of the Federal Republic of Germany to the IAEA in the enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2012. The Government of the Federal Republic of Germany has also made available a statement of the estimated amounts of highly enriched uranium (HEU) as of 31 December 2012 [fr

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of Highly Enriched Uranium

International Nuclear Information System (INIS)

2007-01-01

The Director General has received a Note Verbale dated 3 July 2007 from the Permanent Mission of the Federal Republic of Germany to the IAEA in the enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/549 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2006. The Government of the Federal Republic of Germany has also made available a statement of its annual figures for holdings of civil highly enriched uranium (HEU) as of 31 December 2006 [fr

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2010-01-01

The Director General has received a note verbale dated 14 October 2010 from the Permanent Mission of the Federal Republic of Germany to the IAEA in enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2009. The Government of the Federal Republic of Germany has also made available a statement of its annual figures for holdings of civil high enriched uranium (HEU) as of 31 December 2009 [fr

Communication Received from Germany Concerning its Policies regarding the Management of Plutonium. Statements on the Management of Plutonium and of High Enriched Uranium

International Nuclear Information System (INIS)

2012-01-01

The Secretariat has received a note verbale dated 20 September 2012 from the Permanent Mission of the Federal Republic of Germany to the IAEA in the enclosures of which the Government of Germany, in keeping with its commitment under the Guidelines for the Management of Plutonium (contained in INFCIRC/5491 of 16 March 1998 and hereinafter referred to as the 'Guidelines'), and in accordance with Annexes B and C of the Guidelines, has made available annual figures for holdings of civil unirradiated plutonium and the estimated amounts of plutonium contained in spent civil reactor fuel as of 31 December 2011. The Government of the Federal Republic of Germany has also made available a statement of the estimated amounts of highly enriched uranium (HEU) as of 31 December 2011 [fr

Viability of inert matrix fuel in reducing plutonium amounts in reactors

International Nuclear Information System (INIS)

2006-08-01

Reactors worldwide have produced more than 2000 tonnes of plutonium, contained in spent fuel or as separated forms through reprocessing. Disposition of fissile materials has become a primary concern of nuclear non-proliferation efforts. There is a significant interest in IAEA Member States to develop proliferation resistant nuclear fuel cycles for incineration of plutonium such as inert matrix fuels (IMFs). The present report summarises R and D work on inert matrix fuel for plutonium and (to a lesser extent) minor actinide stock-pile reduction, and discusses the possible strategies to include inert matrix fuel approaches to the nuclear fuel cycle. The publication reviews the status of potential IMF candidates and describes several identified candidate materials for both fast and thermal reactors: MgO, ZrO2, SiC, Zr alloy, SiAl, ZrN; some of these have undergone test irradiations and post-irradiation examination. Also discussed are modelling of IMF fuel performance and safety analysis. System studies have identified strategies for both implementation of IMF fuel as homogeneous or heterogeneous phases, as assemblies or core loadings and in existing reactors in the shorter term, as well as in new reactors in the longer term

Expected behavior of plutonium in the IFR fuel cycle

International Nuclear Information System (INIS)

Steunenberg, R.K.; Johnson, I.

1985-01-01

The Integral Fast Reactor (IFR) is a metal-fueled, sodium-cooled reactor that will consist initially of a U-Zr alloy core in which the enriched uranium will be replaced gradually by plutonium bred in a uranium blanket. The plutonium is concentrated to the required level by extraction from the molten blanket material with a CaCl 2 -BaCl 2 salt containing MgCl 2 as an oxidant (halide slagging). The CaCl 2 -BaCl 2 salt containing dissolved PuCl 3 and UCl 3 is added to the core process where fission products are removed by electrorefining, using a liquid cadmium anode, a metal cathode, and a LiCl-NaCl-CaCl 2 -BaCl 2 molten salt electrolyte. The product is recovered as a metallic deposit on the cathode. The halide slagging step is operated at about 1250 0 and the electrorefining step at about 450 0 C. These processes are expected to give low fission-product decontamination factors of the order of 100

Nonproliferation and safeguards aspects of the Integral Fast Reactor (IFR)

International Nuclear Information System (INIS)

Hannum, W.H.; Wade, D.C.; McFarlane, H.F.; Hill, R.N.

1997-01-01

The National Academy of Sciences (NAS) has declared that the large and growing stocks of plutonium from weapons dismantlement in the U.S. and the former Soviet Union FSU are a ''clear and present danger'' to peace and security. Moreover, the opinion of some experts that plutonium of any isotopic blend is a proliferation threat has been well publicized, heightening the concern that plutonium produced in the civilian fuel cycle is itself a proliferation threat. Assuring that separated plutonium, from dismantled warheads as well as from civilian power programs, is under effective control has (again) become a high priority of U.S. diplomacy. One pole of the debate on how to manage this material is to declare it to be a waste, and to search for some way to dispose of it safely, securely, and permanently. The other pole is to view it as an energy resource and to safeguard it against diversion, putting it into active use in the civilian power program. The ultimate choice cannot be separated from the long-term strategy for use of peaceful nuclear power. Continued use of a once-through fuel cycle will lead to an ever-increasing quantity of excess plutonium-requiring safeguarding. Alternatively, recycling the world's stocks of plutonium in fast reactors, contrary to common misconception, will cap the world supply of plutonium and hold it in working inventories for generating power. Transition from the current-generation light water cooled reactors (LWRs) to a future fast-reactor-based nuclear energy supply under international safeguards would, henceforth, limit world plutonium inventories to the amount necessary and useful for power generation, with no further excess production. (author)

Analysis of fuel cycles with natural uranium, Phase I, Economic analysis of plutonium recycling in BHWR; Analiza gorivnih ciklusa sa prirodnim uranom, II faza - Ekonomska analiza recikliranja plutonijuma u BHWR reaktorima

Energy Technology Data Exchange (ETDEWEB)

Raisic, N; Bosevski, T [Institute of Nuclear Sciences Boris Kidric, Laboratorija za fiziku i dinamiku reaktora, Vinca, Beograd (Serbia and Montenegro)

1965-11-15

The objective of this analysis was establishing a method for determination of the fuel price fraction in the total cost of nuclear power production. Special attention was devoted to recycling of plutonium in natural uranium reactors, plutonium to be used in the same reactor type. The adopted method would enable economic comparison of different types of fuel cycles for different reactors.

Simultaneous determination of plutonium and uranium in environmental samples

International Nuclear Information System (INIS)

Jiao Shufen

1993-01-01

Plutonium and uranium in a plant sample ash was simultaneously determined by using anion exchange resin columns, and concentrated hydrochloric acid and nitric acid. At the final stage of the determination of the nuclides, each of them was electrodeposited together with a little amount of molybdenum carrier onto a stainless steel plate and measured by α-ray spectrometer. The recoveries of uranium and plutonium from the plant samples determined by adding internal standard 236 Pu which was 100% and 63%, respectively

Spectrophotometric determination of uranium and plutonium in nitric acid solutions at their co-presence

International Nuclear Information System (INIS)

Levakov, B.I.; Mishenev, V.B.; Nezgovorov, N.Yu.; Ryazanova, G.K.; Timofeev, G.A.

1986-01-01

The method of spectrophotometric determination of uranium (6) and plutonium (4) in nitric acid solutions is described. Uranium is determined by light absorption of the complex with arsenazo 3 in 0.05 mol/l nitric acid at λ=654 nm, plutonium - by light absorption of the complex with xylenol orange in 0.1 mol/l nitric acid at λ=540 nm. To disguise plutonium, tetravalent and certain trivalent elements DTPA is introduced into photometered solution for uranium determination. The relative root-mean square deviation of determination results does not exceed 0.03 in uranium concenration ranges 0.5-5 μg/ml, of plutonium -1-3 μg/ml

Gas Cooled Fast Reactor Research and Development in the European Union

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