R&D activities based on fast reactor cycle technologies for transmutation of TRU and LLFP by JNC

Research and development(R&D) activities on partitioning and transmutation of trans-uranium nuclides (TRU) and LLFP and future R&D program in JNC were summarized. Feasibility design studies have been conducting to investigate the characteristics of a fast reactor core with TRU and LLFP transmutation. It was reconfirmed that the fast reactor has a strong potential for transmuting TRU and LLFP, effectively. R&D for establishing partitioning process of TRU apart from the high-level radioactive wastes have been carried out. By several counter-current runs of the TRUEX process using highly active raffinates, a process flow sheet capable of selective partitioning of actinides and fission products was newly developed. JNC has settled a new R&D program concerning partitioning and transmutation of long-lived radioactive waste based on recommendation of check & review for OMEGA program performed by the Ad Hoc Committee under the Atomic Energy Commission of Japan (AEC). The R&D program is composed of the design studies and development of element technologies (fabrication, irradiation) in the “Feasibility Studies” on commercialized fast reactor system and the basic studies with experiments (nuclear data, reactor physics, fuel property, etc.) to establish database and analytical tools for the TRU- and LLFP- containing fuel and core design.     

Decomposition of metal carbides as an elementary step of carbon nanotube synthesis

The role of catalyst components in catalysts containing molybdenum, Mo/M/MgO (MNi, Co, and Fe), as well as Mo-free catalysts, M/MgO (MNi, Co, and Fe), for carbon nanotube (CNT) synthesis have been investigated by TEM, XRD, and Raman spectroscopy. CNT synthesis by the catalytic decomposition of CH₄ over M/MgO catalysts can proceed at reaction temperatures higher than the decomposition temperature of the metal carbides (Ni₃C, Co₂C, and Fe₃C), which indicates that carbon in the CNT originates from the graphitic carbon formed on the catalyst surface by the decomposition of metal carbides. For all catalysts containing Mo, thin CNT formation starts at an identical temperature of 923 K, corresponding to the decomposition temperature of MoC_1−x into Mo₂C. The significant effect of the addition of Mo is concerned with the formation of Mo₂C in a catalyst particle during CNT synthesis at high reaction temperatures. The presence of a stable Mo₂C phase leads to the formation of thin CNT with better crystallinity at high reaction temperatures. The role of Ni, Co, and Fe in the Mo/M/MgO catalysts is ascribed to the dissociation of CH₄.