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.     

Reactivity temperature coefficients for the HEU and LEU fuel of the MNSR reactor

Analysis of the Reactivity Temperature Coefficients of the Miniature Neutron Source Reactor (MNSR) for normal and accidental conditions (above 45 °C) using HEU-UAl₄ and the LEU: U₃Si, U₃Si₂ and U9Mo fuel were carried out in this paper. The Fuel Temperature Coefficient (FTC), Moderator Temperature Coefficient (MTC), and Moderator Density Coefficient (MDC) were calculated using the GETERA code. The contribution of each isotope presented in the fuel cell was calculated for the temperature range of 20 °C–100 °C at the beginning of the core life. The average values of the FTC for the UAl₄, U₃Si, U₃Si₂ and U9Mo were found to be: −2.23E-03, −1.85E-02, −1.96E-02, −1.85E-02 mk/°C respectively. The average values of the MTC for the UAl₄, U₃Si, U₃Si₂ and U9Mo were observed to be: −8.91E-03, −1.24E-04, −4.70E-03, 2.10E-03 mk/°C respectively. Finally, the average values of the MDC for the UAl₄, U₃Si, U₃Si₂ and U9Mo were observed to be: −2.06E-01, −2.03E-01, −2.04E-01, −2.03E-01 mk/°C respectively. It's found also that the dominant reactivity coefficient for all types of fuel is the MDC.     

Thermal–hydraulics features of the use of LEU U3Si2 fuel in low-power reactors

Calculations for the use of the U₃Si₂ LEU fuel in low-power research reactors were made. The design basis accident was simulated using the feedback coefficients calculated by the BMAC system. Usability of this fuel in low-power research reactors was demonstrated for both normal daily and accidental operation conditions even if the power of the reactor touches 142 kW during the design basis accident simulation. Both HEU and LEU fuels behave similarly in the normal operation, the temperature of the cladding reaching about 60 °C while higher temperature are obtained for the accidental conditions in the case of the LEU fuel (about 113.7 °C against 98.6 °C for the fuel center temperatures).     

The use of U3Si2 dispersed fuel in Low-Power Research Reactors

The use of U₃Si₂ as a Low Enriched Uranium (LEU) dispersed fuel in Low-Power Research Reactors is investigated in this paper. The fuel proves to be usable if some of the original fuel rods (HEU UAl₄–Al fuel) are still simultaneously employed (mixed core) without changing the structure of the actual core. About 3.5712 mk Initial Excess Reactivity (IER) is procured. Although the worths of both the control rod and the reactivity devices decrease, the safety of these reactors is higher in the case of the new LEU fuel. If the dimensions of the meat and/or the clad are allowed to change these reactors can be run with a meat 2.15 mm outer radius, and a clad 0.58 mm thickness. The IER will then be 4.1537 mk, and both the control rod (CR) worth and the safety margins decrease.     

Plutonium credit in the low enriched uranium fuel of PARR-1

The amount of plutonium (Pu) isotopes and the resultant savings of ²³⁵U due to their production were calculated in the low enriched uranium (LEU) fuel, being utilized in Pakistan Research Reactor-1 (PARR-1). Further the importance map and relative importance map for different isotopes of Pu were also determined. Equilibrium PARR-1 core was achieved for these calculations. MTR-PC26 package was used to generate the microscopic cross-sections data for 45 elements including fissile/structural materials and also the fission products. Finite difference reactor core analysis code CITATION was employed for the fuel management analysis and static depletion calculations.The results indicated that PARR-1 core has attained its equilibrium state after eleven cycles with each cycle of duration about forty full power (10 MW) days. Further, the results showed that at the beginning of equilibrium cycle (BOEC) of the PARR-1 core, net reactivity addition due to all isotopes of Pu was 4.86 × 10⁻³Δk/k. Amount of ²³⁵U equivalent to this value of reactivity was found to be 15.58 ± 0.021 g. Plots of importance and relative importance maps predicted higher isotopic concentrations of Pu in the fuel elements located in the vicinity of central water box.     

Development of very-high-density low-enriched-uranium fuels

Following a hiatus of several years and following its successful development and qualification of 4.8 g U cm⁻³ U₃Si₂–Al dispersion fuel for application with low-enriched uranium in research and test reactors, the US Reduced Enrichment for Research and Test Reactors program has embarked on the development of even-higher-density fuels. Our goal is to achieve uranium densities of 8–9 g cm⁻³ in aluminum-based dispersion fuels. Achieving this goal will require the use of high-density, γ-stabilized uranium alloy powders in conjunction with the most-advanced fuel fabrication techniques. Key issues being addressed are the reaction of the fuel alloys with aluminum and the irradiation behavior of the fuel alloys and any reaction products. Test irradiations of candidate fuels in very-small (micro) plates are scheduled to begin in the Advanced Test Reactor during June, 1997. Initial results are expected to be available in early 1998. We are performing out-of-reactor studies on the phase structure of the candidate alloys on diffusion of the matrix material into the aluminum. In addition, we are modifying our current dispersion fuel irradiation behavior model to accommodate the new fuels. Several international partners are participating in various phases of this work.     

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.     

SCALE calculation for evaluation of spent fuel condition during long-term storage

Experiences with an advanced spent nuclear fuel management in Slovakia are presented in this paper. The evaluation and monitoring procedures are based on practices at the Slovak wet interim spent fuel storage facility in NPP Jaslovské Bohunice. Since 1999, leak testing of WWER-440 fuel assemblies were completed using a special leak tightness detection system developed by Framatome-anp, “Sipping in Pool”. This system utilized external heating for the precise defects determination.Optimal methods for spent fuel disposal and monitoring were designed. A new conservative factor for specifying of spent fuel leak tightness is introduced in the paper. Limit values of leak tightness were established from the combination of SCALE4.4a (ORIGEN-ARP) calculations and measurements from the “Sipping in Pool” system. These limit values are: limiting fuel cladding leak tightness coefficient for tight fuel assembly – k_FCT(T) = 3 × 10⁻¹⁰, limiting fuel cladding leak tightness coefficient for fuel assembly with leakage – k_FCT(L) = 8 × 10⁻⁷.     

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.     

A feasibility study of LEU enrichment uranium fuels for MNSR conversion using MCNP

A neutronics feasibility study has been performed to determine the enrichment that would be required to convert a commercial Miniature Neutron Source Reactor (MNSR) from HEU (90.2%) to LEU (<20%) fuel. Two LEU cores with uranium oxide fuel pins of different dimensions were studied. The one has the same dimensions as the current HEU fuel while the other has the dimensions as the special MNSR, the In-Hospital Neutron Irradiator (INHI), which is a variant of the MNSR. The LEU cores that were studied are of identical core configuration as the current HEU core, except for potential changes in the design of the fuel pins. The following reactor core physics parameters were computed for the two LEU fuel options; clean cold core excess reactivity (ρ_ex), control rod (CR) worth, shut down margin (SDM), neutron flux distributions in the irradiation channels and kinetics data (i.e. effective delayed neutron fraction, β_eff and prompt neutron lifetime, l_f). Results obtained are compared with current HEU core and indicate that it would be feasible to use any of the LEU options for the conversion of NIRR-1 in particular from HEU to LEU.     

Mössbauer study and structural characterization of UO2–Gd2O3 sintered compounds

Samples of UO₂and up to 10 wt% of Gd₂O₃ were prepared by solid-state reaction under a reducing atmosphere, in a thermal path comprising ramps and dwell times in the temperature range of 900–1750 °C. The sintered material was analyzed by X-ray diffraction and ¹⁵⁵Gd Mössbauer spectroscopy. The results showed that for samples annealed up to 900 °C, the gadolinium sesquioxide remained unreacted. However, when the temperature was increased to 1300 °C, a solid-state reaction took place forming mixed oxides. For the more severe sintering condition, at 1750 °C, gadolinia left urania partially unreacted producing a material consisting of two compositions, UO₂ (with no dissolved gadolinium) and (U, Gd)O₂. The proposed heating cycle provided pellets free from Gd₂O₃ phase and may be used by the nuclear fuel industry as a suitable sintering process.     

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.     

Temperature and burnup reactivities and operational lifetime for the submersion-subcritical, safe space (S4) reactor

The He–Xe gas-cooled, S4 reactor has a sectored, Mo–14%Re solid core for avoidance of single point failures in reactor cooling and Closed Brayton Cycle (CBC) energy conversion. The reactor core is loaded with UN fuel and each of its three sectors is thermal-hydraulically coupled to a separate CBC loop and radiator panels. The solid core minimizes voids, and the BeO reflectors are designed to easily disassemble upon impact, ensuring that the bare S4 reactor is sufficiently subcriticial when submerged in wet sand or seawater and flooded with seawater, following a launch abort accident. Spectral shift absorber (SSA) additives in the core and thin SSA coatings on the outer surface of the core can also be used to ensure subcriticality in such an accident. This paper investigates the effects of various SSAs (Re, Ir, Eu-151, B-10 and Gd-155) on the temperature and burnup reactivity coefficients and the operating lifetime of the S4 reactor at a steady thermal power of 550 kW. The calculations of the burnup, reactivity feedback coefficient used a mixture of the top 10 light and top 10 heavy fission products plus Sm-149 and are performed for isothermal reactor core and reflector temperatures of 1200 and 900 K. In this fast spectrum space reactor, SSAs markedly increase fuel enrichment and decrease the burnup reactivity coefficient, but only slightly decrease the temperature, reactivity feedback coefficient. With no SSAs, the UN fuel enrichment is lowest (58.5 wt.%), the temperature and burnup reactivity coefficients are the highest (−0.2709 ¢/K and −1.3470 $/at.%), and the estimated operating lifetime is the shortest (7.6 years). The temperature and burnup reactivity coefficients decrease to −0.2649 ¢/K and −1.0230 $/at.%, and the operating lifetime increases to 8.3 years when rhenium additives are used. With europium-151 and gadolinium-155 additions, fuel enrichment (91.5 and 94 wt.%) and operating lifetime (9.9 and 9.8 years) are the highest and both the temperature reactivity feedback coefficient (−0.2382 and −0.2447 ¢/K) and the burnup reactivity coefficient (−0.9073 and −0.8502 $/at.%) are the lowest.     

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.     

Effects of high density dispersion fuel loading on the uncontrolled reactivity insertion transients of a low enriched uranium fueled material test research reactor

The effects of using high density low enriched uranium on the uncontrolled reactivity insertion transients of a material test research reactor were studied. For this purpose, the low density LEU fuel of an MTR was replaced with high density U–Mo (9w/o) LEU fuels currently being developed under the RERTR program having uranium densities of 6.57 gU/cm³, 7.74 gU/cm³ and 8.57 gU/cm³. Simulations were carried out to determine the reactor performance under reactivity insertion transients with totally failed control rods. Ramp reactivities of 0.25$/0.5 s and 1.35$/0.5 s were inserted with reactor operating at full power level of 10 MW. Nuclear reactor analysis code PARET was employed to carry out these calculations. It was observed that when reactivity insertion was 0.25$/0.5 s, the new power level attained increased by 5.8% as uranium density increases from 6.57 gU/cm³ to 8.90 gU/cm³. This results in increased maximum temperatures of fuel, clad and coolant outlet, achieved at the new power level, by 4.7 K, 4.4 K and 2.4 K, respectively. When reactivity insertion was 1.35$/0.5 s, the feedback reactivities were unable to control the reactor which resulted in the bulk boiling of the coolant; the one with the highest fuel density was the first to reach the boiling point.     

Design and experience of HEU and LEU fuel for WWR-M reactors

Thin-walled WWR-M5 fuel elements were designed and manufactured and have been used successfully for 16 years; they contain twice as much uranium-235 as the WWR-M2 and WWR-M3 fuel elements. The fuel elements have been optimized with regard to their neutron physics and thermal-hydraulic parameters and fuel consumption has been minimized. The mean specific power in the core of the WWR-M reactor was raised to 230 kW l⁻¹, the measured maximum volume thermal specific power was 900±100 kW l⁻¹ and the surface specific power was 136±15 W cm⁻². The WWR-M5 fuel elements enable the power of the WWR-M pooltype reactor to be raised to 30 MW while simultaneously increasing the number of cells in the core available for experimentation by a factor of approximately two and reducing fuel element consumption. Reactor tests of WWR-M fuel elements with reduced fuel enrichment (36 and 21%) were carried out for a meat uranium density up to 2–3 g cm⁻³. Conversion of WWR-SM-type reactors to these fuel elements did not lead to a loss in reactivity and enabled their power to be increased to 20–30 MW.     

Ion irradiation induced nanocrystal formation in amorphous Zr55Cu30Al10Ni5 alloy

Ion irradiation can be used to induce partial crystallization in metallic glasses to improve their surface properties. We investigated the microstructural changes in ribbon Zr₅₅Cu₃₀Al₁₀Ni₅ metallic glass after 1 MeV Cu-ion irradiation at room temperature, to a fluence of 1.0 × 10¹⁶ cm⁻². In contrast to a recent report by others that there was no irradiation induced crystallization in the same alloy [S. Nagata, S. Higashi, B. Tsuchiya, K. Toh, T. Shikama, K. Takahiro, K. Ozaki, K. Kawatusra, S. Yamamoto, A. Inouye, Nucl. Instr. and Meth. B 257 (2007) 420], we have observed nanocrystals in the as-irradiated samples. Two groups of nanocrystals, one with diameters of 5–10 nm and another with diameters of 50–100 nm are observed by using high resolution transmission electron microscopy. Experimentally measured planar spacings (d-values) agree with the expectations for Cu₁₀Zr₇, NiZr₂ and CuZr₂ phases. We further discussed the possibility to form a substitutional intermetallic (Ni_xCu_1−x)Zr₂ phase.     

JR curves of the low alloy steel 20 MnMoNi 5 5 with two different sulphur contents in oxygen-containing high temperature water at 240°C

J_R curves of the low alloy steel 20 MnMoNi 5 5 with two different sulphur contents (0.003 and 0.011 wt.%) were determined at 240°C in oxygen-containing high temperature water as well as in air. The tests were performed by the single-specimen unloading compliance technique at load line displacement rates from 1 × 10⁻⁴ down to 1 × 10⁻⁶ mm s⁻¹ on 20% side-grooved 2T CT specimens in an autoclave testing facility at an oxygen content of 8 ppm and a pressure of 7 MPa under quasi-stagnant flow conditions.In the case of testing in high temperature water, remarkably lower J_R curves than in air at the same load line displacement rate (1 × 10⁻⁴ mm s⁻¹) were obtained. A decrease in the load line displacement rate as well as an increase in the sulphur content of the steel caused a reduction of the J_R curves. At the fastest load line displacement rate a stretch zone could be detected fractographically on the specimens tested in air and in high temperature water and consequently J_i could be determined. When testing in high temperature water, the J_i value of the higher sulphur material type decreases from 45 N mm⁻¹ in air to 3 N mm⁻¹, much more than that of the optimized material type from 51 N mm⁻¹ in air to 20 N mm⁻¹ at 1 × 10⁻⁴ mm s⁻¹.     

Criticality investigations for the fixed bed nuclear reactor using thorium fuel mixed with plutonium or minor actinides

Prospective fuels for a new reactor type, the so called fixed bed nuclear reactor (FBNR) are investigated with respect to reactor criticality. These are ① low enriched uranium (LEU); ② weapon grade plutonium + ThO₂; ③ reactor grade plutonium + ThO₂; and ④ minor actinides in the spent fuel of light water reactors (LWRs) + ThO₂. Reactor grade plutonium and minor actinides are considered as highly radio-active and radio-toxic nuclear waste products so that one can expect that they will have negative fuel costs.The criticality calculations are conducted with SCALE5.1 using S₈–P₃ approximation in 238 neutron energy groups with 90 groups in thermal energy region. The study has shown that the reactor criticality has lower values with uranium fuel and increases passing to minor actinides, reactor grade plutonium and weapon grade plutonium.Using LEU, an enrichment grade of 9% has resulted with k_eff = 1.2744. Mixed fuel with weapon grade plutonium made of 20% PuO₂ + 80% ThO₂ yields k_eff = 1.2864. Whereas a mixed fuel with reactor grade plutonium made of 35% PuO₂ + 65% ThO₂ brings it to k_eff = 1.267. Even the very hazardous nuclear waste of LWRs, namely minor actinides turn out to be high quality nuclear fuel due to the excellent neutron economy of FBNR. A relatively high reactor criticality of k_eff = 1.2673 is achieved by 50% MAO₂ + 50% ThO₂.The hazardous actinide nuclear waste products can be transmuted and utilized as fuel in situ. A further output of the study is the possibility of using thorium as breeding material in combination with these new alternative fuels.