Reactivity feedbacks of a material test research reactor fueled with various low enriched uranium dispersion fuels

The reactivity feedbacks of a material test research reactor using various low enriched uranium fuels, having same uranium density were calculated. For this purpose, the original aluminide fuel (UAl_x–Al) containing 4.40 gU/cm³ of an MTR was replaced with silicide (U₃Si–Al and U₃Si₂–Al) and oxide (U₃O₈–Al) dispersion fuels having the same uranium density as of the original fuel. Calculations were carried out to find the fuel temperature reactivity feedback, moderator temperature reactivity feedback, moderator density reactivity feedback and moderator void reactivity feedback. Nuclear reactor analysis codes including WIMS-D4 and CITATION were employed to carry out these calculations. It was observed that the magnitudes all the respective reactivity feedbacks from 38 °C to 50 °C and 100 °C, at the beginning of life, of all the fuels were very close to each other. The fuel temperature reactivity feedback of the U₃O₈–Al was about 2% more than the original UAl_x–Al fuel. The magnitudes of the moderator temperature, moderator density and moderator void reactivity feedbacks of all the fuels, showed very minor variations from the original aluminide fuel.     

Kr ion irradiation study of the depleted-uranium alloys

Fuel development for the reduced enrichment research and test reactor (RERTR) program is tasked with the development of new low enrichment uranium nuclear fuels that can be employed to replace existing high enrichment uranium fuels currently used in some research reactors throughout the world. For dispersion type fuels, radiation stability of the fuel-cladding interaction product has a strong impact on fuel performance. Three depleted-uranium alloys are cast for the radiation stability studies of the fuel-cladding interaction product using Kr ion irradiation to investigate radiation damage from fission products. SEM analysis indicates the presence of the phases of interest: U(Al, Si)₃, (U, Mo)(Al, Si)₃, UMo₂Al₂₀, U₆Mo₄Al₄₃ and UAl₄. Irradiations of TEM disc samples were conducted with 500 keV Kr ions at 200 °C to ion doses up to 2.5 × 10¹⁹ ions/m² (∼10 dpa) with an Kr ion flux of 10¹⁶ ions/m²/s (∼4.0 × 10⁻³ dpa/s). Microstructural evolution of the phases relevant to fuel-cladding interaction products was investigated using transmission electron microscopy.     

Irradiation behavior of atomized U–10wt.% Mo alloy aluminum matrix dispersion fuel meat at low temperature

In order to examine the in-reactor behavior of very-high-density dispersion fuels for high flux performance research reactors, U–10wt.% Mo alloy dispersions in an aluminum matrix have been irradiated at low temperature in the Advanced Test Reactor (ATR). The alloy fuel dispersant was produced by a centrifugal atomization process. The fuel shows stable in-reactor irradiation behavior to a fission density of 5×10²⁷ m⁻³ at an irradiation temperature of 65 °C. The fuel–matrix interaction layer growth rate is similar to that observed in uranium-silicide fuels. The fuel particles have a fine and a relatively narrow fission gas bubble size distribution. There appears to be features in the microstrucure that are the result of segregation of the microstructure in to molybdenum rich and depleted regions on solidification.     

Short-term irradiation behavior of minor actinide doped uranium plutonium mixed oxide fuels irradiated in an experimental fast reactor

A fuel irradiation program is being conducted using the experimental fast reactor ‘Joyo’. Two short-term irradiation tests in the program were completed in 2006 using a uranium and plutonium mixed oxide fuel which contains minor actinides (MA-MOX fuel). The objective of the tests is the investigation of early thermal behavior of MA-MOX fuel such as fuel restructuring and redistribution of minor actinides. Three fuel pins which contained MA-MOX: 2% neptunium and 2% americium doped uranium plutonium mixed oxide (Am,Pu,Np,U)O_2−x fuel were supplied for testing. The first test was conducted with high-linear heating rate of approximately 430 W cm⁻¹ for only 10 min. After the first test, one fuel pin was removed for examinations. Then the second test was conducted with the remaining two pins at nearly the same linear power for 24 h. In these tests, two oxygen-to-metal molar ratios were used for fuel pellets as a test parameter. Non-destructive and destructive post-irradiation examinations results are discussed with early on the behavior of the fuel during irradiation.     

Neutronic analysis for core conversion (HEU–LEU) of Pakistan research reactor-2 (PARR-2)

Neutronic analyses for the core conversion of Pakistan research reactor-2 (PARR-2) from high enriched uranium (HEU) fuel to low enriched uranium (LEU) fuel has been performed. Neutronic model has been verified for 90.2% enriched HEU fuel (UAl₄–Al). For core conversion, UO₂ fuel was chosen as an appropriate fuel option because of higher uranium density. Clad has been changed from aluminum to zircalloy-4. Uranium enrichment of 12.6% has been optimized based on the design basis criterion of excess reactivity 4 mk in miniature neutron source reactor (MNSR). Lattice calculations for cross-section generation have been performed utilizing WIMS while core modeling was carried out employing three dimensions option of CITATION. Calculated neutronic parameters were compared for HEU and LEU fuels. Comparison shows that to get same thermal neutron flux at inner irradiation sites, reactor power has to be increased from 30 to 33 kW for LEU fuel. Reactivity coefficients calculations show that doppler and void coefficient values of LEU fuel are higher while moderator coefficient of HEU fuel is higher. It is concluded that from neutronic point of view LEU fuel UO₂ of 12.6% enrichment with zircalloy-4 clad is suitable to replace the existing HEU fuel provided that dimensions of fuel pin and total number of fuel pins are kept same as for HEU fuel.     

Test irradiations of full-sized U3Si2-Al fuel plates up to very high fission densities

In the course of the licensing procedure of the ‘Forschungsneutronenquelle Heinz Maier-Leibnitz’, i.e. the new 20 MW high-flux research reactor FRM II in Garching near Munich, extensive test irradiations have been performed to qualify the U₃Si₂-Al dispersion fuel with a relatively high density of highly enriched uranium (93 wt% of ²³⁵U) up to very high fission densities. Two of the three FRM II type fuel plates used in the irradiation tests contained U₃Si₂-Al dispersion fuel with HEU densities of 3.0 gU/cm³ or 1.5 gU/cm³ (‘homogeneous plates’) and one plate had two adjacent zones of either density (‘mixed plate’). They were irradiated in the French MTR reactors SILOE and OSIRIS in the years before 2002. The local plate thickness was measured on certain tracks along the plates during interruptions of the irradiation. The maximum fission density obtained in the U₃Si₂ fuel particles was 1.4 × 10²² f/cm³ and 1.1 × 10²² f/cm³ in the 1.5 gU/cm³ and 3.0 gU/cm³ fuel zones, respectively. In the course of the irradiations, the plate thickness increased monotonically and approximately linearly, leading to a maximum plate thickness swelling of 14% and 21% and a corresponding volume increase of the fuel particles of 106% and 81%, respectively. Our results are discussed and compared with the data from the literature.     

Kinetic parameters of a material test research reactor fueled with various low enriched uranium dispersion fuels

The effects of using different low enriched uranium fuels, having same uranium density, on the kinetic parameters of a material test research reactor were studied. For this purpose, the original aluminide fuel (UAl_x-Al) containing 4.40 gU/cm³ of an MTR was replaced with silicide (U₃Si-Al and U₃Si₂-Al) and oxide (U₃O₈-Al) dispersion fuels having the same uranium density as of the original fuel. Simulations were carried out to calculate prompt neutron generation time, effective delayed-neutron fraction, core excess reactivity and neutron flux spectrum. Nuclear reactor analysis codes including WIMS-D4 and CITATION were used to carry out these calculations. It was observed that both the silicide fuels had the same prompt neutron generation time 0.02% more than that of the original aluminide fuel, while the oxide fuel had a prompt neutron generation time 0.05% less than that of the original aluminide fuel. The effective delayed-neutron fraction decreased for all the fuels; the decrease was maximum at 0.06% for U₃Si₂-Al followed by 0.03% for U₃Si-Al, and 0.01% for U₃O₈-Al fuel. The U₃O₈-Al fueled reactor gave the maximum ρ_excess at BOL which was 21.67% more than the original fuel followed by U₃Si-Al which was 2.55% more, while that of U₃Si₂-Al was 2.50% more than the original UAl_x-Al fuel. The neutron flux of all the fuels was more thermalized, than in the original fuel, in the active fuel region of the core. The thermalization was maximum for U₃O₈-Al followed by U₃Si-Al and then U₃Si₂-Al fuel.     

Temperature and dose dependence of fission-gas-bubble swelling in U3Si2

Large fission gas bubbles were observed during metallographic examination of an irradiated U₃Si₂ dispersion fuel plate (U0R040) in the Advanced Test Reactor (ATR). The fuel temperature of this plate was higher than for most of the previous silicide-fuel tests where much smaller bubble growth was observed. The apparent conditions for the large bubble growth are high fission density (6.1 × 10²¹ f/cm³) and high fuel temperature (life-average 160 °C). After analysis of PIE results of U0R040 and previous ANL test plates, a modification to the existing athermal bubble growth model appears to be necessary for high temperature application (above 130 °C). A detailed analysis was performed using a model for the irradiation-induced viscosity of binary alloys to explain the effect of the increased fuel temperature. Threshold curves are proposed in terms of fuel temperature and fission density above which formation and interconnection of bubbles larger than 5 μ are possible.     

Electric conductivity of neutron-irradiated aluminum alloys

The effect of ionizing radiation, temperature, and products of the radiolysis of water on the materials of fuel elements used in nuclear reactors during operation is examined. The effect of irradiation in a reactor on the electric conductivity and the change of the linear dimensions of the alloys SAV-1 and AMG-2 are investigated. It can be concluded on the basis of the relative elongation that the aluminum alloys studied can be used to fluence 10²⁰ cm⁻² without appreciable loss of reliability.     

Uranium-molybdenum nuclear fuel plates behaviour under heavy ion irradiation: An X-ray diffraction analysis

Heavy ion irradiation has been proposed for discriminating UMo/Al specimens which are good candidates for research reactor fuels. Two UMo/Al dispersed fuels (U-7 wt%Mo/Al and U-10 wt%Mo/Al) have been irradiated with a 80 MeV ¹²⁷I beam up to an ion fluence of 2 × 10¹⁷ cm⁻². Microscopy and mainly X-ray diffraction using large and micrometer sized beams have enabled to characterize the grown interaction layer: UAl₃ appears to be the only produced crystallized phase. The presence of an amorphous additional phase can however not be excluded. These results are in good agreement with characterizations performed on in-pile irradiated fuels and encourage new studies with heavy ion irradiation.     

An innovative research reactor design

A new and innovative core design for a research reactor is presented. It is shown that while using the standard, low enriched uranium as fuel, the maximum thermal flux per MW of power for the core design suggested and analyzed here is greater than those found in existing state of the art facilities without detrimentally affecting the other design specs. A design optimization is also carried out to achieve the following characteristics of a pool type research reactor of 10 MW power: high thermal neutron fluxes; sufficient space to locate facilities in the reflector; and an acceptable life cycle. In addition, the design is limited to standard fuel material of low enriched uranium. More specifically, the goal is to maximize the maximum thermal flux to power ratio in a moderate power reactor design maintaining, or even enhancing, other design aspects that are desired in a modern state of the art multi-purpose facility. The multi-purpose reactor design should allow most of the applications generally carried out in existing multi-purpose research reactors. Starting from the design of the German research reactor, FRM-II, which delivers high thermal neutron fluxes, an azimuthally asymmetric cylindrical core design with an inner and outer reflector, is developed. More specifically, one half of the annular core (0 < θ < π) is thicker than the other half. Two variations of the design are analyzed using MCNP, ORIGEN2 and MONTEBURNS codes. Both lead to a high thermal flux zone, a moderate thermal flux zone, and a low thermal flux zone in the outer reflector. Moreover, it is shown that the inner reflector is suitable for fast flux irradiation positions. The first design leads to a life cycle of 41 days and high, moderate and low (non-perturbed) thermal neutron fluxes of 4.2 × 10¹⁴ n cm⁻² s⁻¹, 3.0 × 10¹⁴ n cm⁻² s⁻¹, and 2.0 × 10¹⁴ n cm⁻² s⁻¹, respectively. Heat deposition in the cladding, coolant and fuel material is also calculated to determine coolant flow rate, coolant outlet temperature and maximum fuel temperature under steady-state operating conditions. Finally, a more compact version of the asymmetric core is developed where a maximum (non-perturbed) thermal flux of 5.0 × 10¹⁴ n cm⁻² s⁻¹ is achieved. The core life of this more compact version is estimated to be about 23 days.     

Minimization of actinide waste by multi-recycling of thoriated fuels in the EPR reactor

The multi-recycling of innovative uranium/thorium oxide fuels for use in the European Pressurized water Reactor (EPR) has been investigated. If increasing quantities of ²³⁸U, the fertile isotope in standard UO₂ fuel, are replaced by ²³²Th, then a greater yield of new fissile material (²³³U) is produced during the cycle than would otherwise be the case. This leads to economies of natural uranium of around 45% if the uranium in the spent fuel is multi-recycled. In addition we show that minor actinide and plutonium waste inventories are reduced and hence waste radio-toxicities and decay heats are up to a factor of 20 lower after 10³ years. Two innovative fuel types named S90 and S20, ThO₂ mixed with 90% and 20% enriched UO₂ respectively, are compared as an alternative to standard uranium oxide (UOX) and uranium/plutonium mixed oxide (MOX) fuels at the longest EPR fuel discharge burn-ups of 65 GWd/t. Fissile and waste inventories are examined, waste radio-toxicities and decay heats are extracted and safety feedback coefficients are calculated. Finally, we discuss the economics of such strategies.     

Post-irradiation examination of uranium-7 wt% molybdenum atomized dispersion fuel

Two low-enriched uranium fuel plates consisting of U-7wt%Mo atomized powder dispersed in an aluminum matrix, have been irradiated in the FUTURE irradiation rig of the BR2 reactor at SCK•CEN. The plates were submitted to a heat flux of maximum 353 W/cm² while the surface cladding temperature is kept below 130 °C. After 40 full power days, visual examination and profilometry of the fuel plates revealed an increase of the plate thickness. In view of this observation, the irradiation campaign was prematurely stopped and the fuel plates were retrieved from the reactor, having at their end-of-life a maximum burn-up of 32.8% ²³⁵U (6.5% FIMA). The microstructure of one of the fuel plates has been characterized in an extensive post-irradiation campaign. The U(Mo) fuel particles have been found to interact with the Al matrix, resulting in an interaction layer which can be identified as (U,Mo)Al₃ and (U,Mo)Al₄. Based on the composition of the interaction layer it is shown that the observed physical parameters like thickness of the interaction layer between the Al matrix and the U(Mo) fuel particles compare well to the values calculated by the MAIA code, an U(Mo) behavior modeling code developed by the Commissariat à l’énergie atomique (CEA).     

Neutron flux determination in irradiation sites of an Am–Be neutron source at NNRI

Neutron flux measurements and flux distribution parameters for two irradiation sites of an Am–Be neutron source irradiator were measured by using gold (Au), zirconium (Zr) and aluminum (Al) foils. thermal neutron flux Φ_th = 1.46 × 10⁴ n cm⁻² s⁻¹ ± 0.01 × 10², epithermal neutron flux Φ_epi = 7.23 × 10² n cm⁻² s⁻¹ ± 0.001, fast neutron flux Φ_f = 1.26 × 10² n cm⁻² s⁻¹ ± 0.020, thermal-to-epithermal flux ratio f = 20.5 ± 0.36 and epithermal neutron shaping factor α = −0.239 ± 0.003 were found for irradiation Site-1; while the thermal neutron flux Φ_th = 4.45 × 10³ n cm⁻² s⁻¹ ± 0.06, the epithermal neutron Φ_epi = 1.50 × 10² n cm⁻² s¹ ± 0.003, the fast neutron flux Φ_f = 1.17 × 10 n cm⁻² s⁻¹ ± 0.011, thermal-to-epithermal flux ratio f = 29.6 ± 0.94, and epithermal neutron shaping factor α = 0.134 ± 0.001 were found for irradiation Site-2. It was concluded that the Am–Be neutron source can be used for neutron activation analysis (NAA). The Am–Be source can be used for neutron activation analysis thereby reducing the burden on GHARR-1 and increasing the research output of the nation.     

Effect of external gamma irradiation on dissolution of the spent UO2 fuel matrix

Leaching experiments were performed on UO₂ pellets doped with alpha-emitters (^238/239Pu) and on spent fuel, in the presence of an external gamma irradiation source (A⁶⁰Co = 260 Ci,  Gy h⁻¹). The effects of α, β, γ radiation, the fuel chemistry and the nature of the cover gas (aerated or Ar + 4%H₂) on water radiolysis and on oxidizing dissolution of the UO₂ matrix are quantified and discussed. For the doped UO₂ pellets, the nature of the cover gas clearly has a major role in the effect of gamma radiolysis. The uranium dissolution rate in an aerated medium is 83 mg m⁻² d⁻¹ compared with only 6 mg m⁻² d⁻¹ in Ar + 4%H₂. The rate drop is accompanied by a reduction of about four orders of magnitude in the hydrogen peroxide concentrations in the homogeneous solution. The uranium dissolution rates also underestimate the matrix alteration rate because of major precipitation phenomena at the UO₂ pellet surface. The presence of studtite in particular was demonstrated in aerated media; this is consistent with the measured H₂O₂ concentrations (1.2 × 10⁻⁴ mol L⁻¹). For spent fuel, the presence of fission products (Cs and Sr), matrix alteration tracers, allowed us to determine the alteration rates under external gamma irradiation. The fission product release rates were higher by a factor of 5-10 than those of the actinides (80-90% of the actinides precipitated on the surface of the fragments) and also depended to a large extent on the nature of the cover gas. No significant effect of the fuel chemistry compared with UO₂ was observed on uranium dissolution and H₂O₂ production in the presence of the ⁶⁰Co source in aerated conditions. Conversely, in Ar + 4%H₂ the fuel self-irradiation field cannot be disregarded since the H₂O₂ concentrations drop by only three orders of magnitude compared with UO₂.     

UO2 dissolution in Boom Clay conditions

The solubility of uranium dioxide (UO₂) was measured in real and synthetic Boom Clay waters with varying concentrations of humic acids and carbonate under reducing conditions at 20 °C. Uranium concentrations in function of time suggest the reduction of U(VI) to U(IV) by the humic acids which is occurring faster in real clay water than in synthetic clay waters. Humic acids induce also a competition to complex U(VI) in carbonate-containing solution, but they are not able to control the uranium concentration at high bicarbonate concentration (0.02 mol dm⁻³). Nevertheless they may play a role at low carbonate concentration. In our experimental conditions, the geochemical calculations indicate that two uranium secondary phases (U₄O₉ and UO_2(c)) are susceptible to control the uranium concentration in solution. These calculations are in good agreement with results of the X-ray photoelectron spectroscopy. At the end of tests, uranium concentrations reach steady-state values between 3 × 10⁻⁸ and 5 × 10⁻⁸ mol dm⁻³ in the bicarbonate-rich solutions. Although these concentrations are considered as conservative, they are 10-100 times higher than in natural Boom Clay. The consequence is that spent fuel could slowly dissolve in the interstitial clay water undersaturated with respect to UO₂/UO_2+x of the fuel.     

Gas phase in experimental fuel elements with compact uranium dioxide,irradiated in the SM-2 reactor

Conclusions A complex procedure has been developed for the study of gas release from nuclear fuel, including reactor measurements and post-reactor determination of the amount and composition of the gas medium in the fuel elements at room and elevated temperatures. In fuel elements with compact uranium dioxide (density 10.0–10.43 g/cm³), in addition to gaseous fission products and the helium introduced, Ar, H₂, O₂, CO, CO₂, and N₂ are present, and after irradiation their quantity exceeds the initial quantity, measured for unirradiated fuel elements, by a factor of several.The yield of Xe and Kr under the can of the fuel elements during irradiation of uranium dioxide in the SM-2 reactor amounts to 30–50%, but the measured ratio of Xe/Kr exceeds the calculated ratio by a factor of 1.2, because of the reaction¹³⁵Xe(n, )¹³⁶Xe. The content in the fuel of adsorbed helium is equal to 0.004 n.cm³/g UO₂. The data obtained can be used for physics and technological calculations, and also for refining the procedure for the determination of gas release.Translated from Atomnaya Énergiya, Vol. 57, No. 2, pp. 91–95, August, 1984.     

Neutronic analysis of PROMETHEUS reactor fueled with various compounds of thorium and uranium

In this study, neutronic performance of the DT driven blanket in the PROMETHEUS-H (heavy ion) fueled with different fuels, namely, ThO₂, ThC, UO₂, UC, U₃Si₂ and UN is investigated. Helium is used as coolant, and SiC is used as cladding material to prevent fission products from contaminating coolant and direct contact fuel with coolant in the blanket. Calculations of neutronic data per DT fusion neutron are performed by using SCALE 4.3 Code. M (energy multiplication factor) changes from 1.480 to 2.097 depending on the fuel types in the blanket under resonance-effect. M reaches the highest value in the blanket fueled with UN. Therefore, the investigated reactor can produce substantial electricity in situ. UN has the highest value of ²³⁹Pu breeding capability among the uranium fuels whereas UO₂ has the lowest one. ²³⁹Pu production ratio changes from 0.119 to 0.169 according to the uranium fuel types, and ²³³U production values are 0.125 and 0.140 in the blanket fueled with ThO₂ and ThC under resonance-effect, respectively. Heat production per MW (D,T) fusion neutron load varies from 1.30 to 7.89 W/cm³ in the first row of fissile fuel breeding zone depending on the fuel types. Heat production attains the maximum value in the blanket fueled with UN. Values of TBR (tritium breeding ratio) being one of the most important parameters in a fusion reactor are greater than 1.05 for all type of fuels so that tritium self-sufficiency is maintained for DT fusion driver. Values of peak-to-average fission power density ratio, Γ, are in the range of 1.390 and ∼1.476 depending on the fuel types in the blanket. Values of neutron leakage out of the blanket for all fuels are quite low due to SiC reflector. The maximum neutron leakage is only ∼0.025. Consequently, for all cases, the investigated reactor has high neutronic performance and can produce substantial electricity in situ, fissile fuel and tritium required for (D,T) fusion reaction.     

Medium energy ion irradiation capability for studies of radiation damage effects over a wide temperature range

In this report, we present preliminary ion irradiation experiments performed using a new medium energy (up to ∼20 MeV), high temperature ion irradiation capability that we developed at Los Alamos National Laboratory. Details of ion fluence and irradiation temperature (including ion beam heating) control, measurements procedure and accuracy are described. In particular, we investigated irradiation-induced atomic intermixing in a layered structure composed of MgO and HfO₂ thin films deposited on a sapphire substrate. This multi-layered structure represents a dispersion nuclear fuel form surrogate. To simulate a nuclear reactor environment, we performed ion irradiation using 10 MeV Au ions to a fluence of 5 × 10¹⁵ cm⁻² at a substrate temperature of 1000 °C. The degree of atomic intermixing was assessed from depth profiles of Mg, Hf, and Al atoms, which were obtained using Rutherford backscattering spectrometry. We found considerable interlayer mixing for sample regions in close proximity to the sapphire substrate.     

A neutronic evaluation of the (Pu–U) and (Am–Pu–U) insertion in a typical fuel of Angra-I

The goal is to evaluate the neutronic behavior when (Pu–U) and (Am–Pu–U) mixed oxide are inserted in a typical cell of a Pressurized Water Reactor (PWR) such as Angra-I. Four types of fuels were studied: (1) MOX fuel enriched at 3.1% and V_m/V_f = 1.15; (2) MOX fuel enriched at 4.5% and V_m/V_f = 1.15; (3) MOX fuel enriched at 4.5% and V_m/V_f = 2.0 and (4) MOX fuel enriched at 4.5%, with 1% of Americium insertion in its composition (62.8% of Am²⁴¹, 0.1% of Am^242m and 37.1% of Am²⁴³) and with V_m/V_f = 2.0. The first case represents the standard state of Angra I, but with Pu. The second case is similar to the first but the enrichment is increased. To evaluate the Americium insertion, a study of the V_m/V_f was made and better results were obtained with V_m/V_f = 2.0 and to compare, this case was too evaluated to (Pu–U) in the third and fourth cases. The idea is to verify the possibility of using these fuels in Angra-I analyzing neutronic parameters such as infinite multiplication factor, hardening spectrum, Boron worth and reactivity temperature coefficients. The results show that it is possible to use all the studied fuels in Angra-I as well as to burn Am inserted in the MOX fuel by a considerable quantity during PWR operation. The WIMS-D5 code was used to perform a simplified neutronic and burnup simulations to evaluate this possibility.