Date Kathryn McCarthy, Systems Analysis Campaign Director Date iii
Executive SummaryThe primary focus of this work is a comparison between MgO and UO 2 as matrix material options for burning minor actinides (MA) in transmutation targets within a sodium cooled fast reactor. The heterogeneous sodium fast reactor considered in this analysis was adapted from the homogeneous Advanced Burner Reactor.[2] In a previous work by Idaho National Laboratory, MgO and UO 2 target matrix options were compared based on identical target geometry.[3] Thus, the TRU conversion ratio (CR) was allowed to change due to excess TRU breeding in the UO 2 matrix. In this work, the fuel volume fraction was changed in order to match the CR between the UO 2 and MgO cases at approximately 0.75. This was done in order to provide a comparison of the two matrix materials based on similar net TRU destruction rates. The number of target assemblies was kept the same in each heterogeneous case (48) and approximately the same cycle length was used since it was limited by the fluence in the outer driver zone. The cycle length was set by limiting each assembly in the core to 200 dpa during its life. Also, the mass ratio of MAs (Am+Cm+Cf+Bk) to Np+Pu in the external supply of TRU was held constant and equal to that found in LWR SNF. For the purpose of this study, neptunium is excluded from the definition of "minor actinide".The UO 2 matrix-based targets required a 30% higher MA loading in order to achieve the same net MA destruction rate as the targets with an inert MgO matrix. The larger MA loading for the UO 2 case is due to the fact that the UO 2 case has a smaller transmutation efficiency than the MgO case. The MA destruction efficiency (EMA) of the targets is defined as the absolute value of the MA mass in a target assembly at discharge minus the amount charged in a fresh assembly, divided by the amount in the fresh assembly. The transmutation efficiency is 33% and 43%, for the UO 2 and MgO case respectively. The reduced transmutation efficiency of UO 2 is caused by the breeding of TRU from U-238 during the target's 10 cycle irradiation. During the irradiation time, the successive neutron captures from this bred TRU, eventually produce and accumulate MAs within the target. Due to the introduction of this internal source of MAs in the fuel cycle of the UO 2 matrix, the MA charge rate must be increased in order to maintain the same net MA destruction rate as in the MgO case. This is achieved by increasing the MA concentration in the targets (target enrichment).Assuming that the two matrix materials release the same fraction of fission gasses produced, the higher MA actinide inventory present in the targets having UO 2 matrix leads to higher fission gas pressures in the target pins, since they will have more fissions occurring during their core residence time. In this analysis, the calculated gas pressures in the UO 2 matrix targets were higher still due to the lower fuel volume fraction in these targets. However, even if compared on a basis of equal sp...