Self-Powered Neutron Detector (SPND) is one of devices for in-core fluxes detecting without external electricity source. SPND consisted with emitter, insulator and collector. When neutrons reacted with emitter material, it generates electrons and these electrons cross insulator area to make electric signal in collector area. For calculating sensitivity of SPND with Monte-Carlo code such as MCNP, many physical components must be considered. Cobalt shows that prompt signal and relatively low signal comparing with other delayed signal SPNDs. Initial sensitivity was calculated as 4.28×10−22 A/nv-cm for one electron. Due to Cobalt’s complex decay chain and maintaining high efficiency of SPND, it is necessary to analysis the effect of activation of emitter. Therefore, the DPA (Displacements Per Atom) assessment and activation analysis of the detector components have been evaluated with MCNP 6.2 and ORIGEN-S. With these activation analysis results, that is expected to be used to determine the shielding thickness of the storage system.

The purpose of full system decontamination before decommissioning a nuclear power plant is to reduce radiation exposure of decommissioning workers and to reduce decommissioning waste. In general, full system decontamination removes the CRUD nuclides deposited on the inner surface of the reactor coolant system, chemical and volume control system, residual heat removal system, pressurizer, steam generator tube, etc. by chemical decontamination method. The full system decontamination process applied to Maine Yankee and Connecticut Yankee in the USA, Stade, Obrigheim, Unterweser, Nekawestheim Unit 1 in Germany, Mihama Unit 1 and 2 in Japan, Jose Cabrera Unit 1 in Spain, and Barseback Unit 1 and 2 in Sweden are HP/CORD UV, NP/CORD UV, and DfD. In this study, the quantity of 60Co radioactivity removal, metal removal, ion exchange resin and filter generation according to reactor power, surface area and volume of the full system decontamination flow path, and the decontamination process were compared and analyzed. In addition, the quantity of 60Co radioactivity removal by each nuclear power plant was compared and analyzed with the evaluation results of the 60CO radioactivity inventory of the Kori Unit 1 full system decontamination loops conducted by SAE-AN Enertech Corporation.

Numerous low-and intermediate level radioactive wastes were generated from the decommissioning processes of nuclear power plants. Radionuclides such as Co and Cs contained in decommissioning wastes should be immobilized to prevent the release of radionuclides from the wastes due to its harmful impacts on ecosystem by high radioactivity and long half-life. Ethylenediaminetetraacetic acid (EDTA) used as decontamination agent can be contained in cement waste during decommissioning process of nuclear power plants. In addition, EDTA can be stably and strongly bound with radionuclides, resulting in the acceleration of the nuclide release from solidified cement matrix. Here, we investigated the effects of EDTA on leaching behaviors of Co and Cs immobilized in the cement specimen. The leaching tests were performed according to the ANS 16.1 “Measurement of the leachability of solidified low-level radioactive wastes by a short-term test procedure”. From the results, an increase in the EDTA content in the cement specimen led to an increase in Co leaching, whereas a decrease in Cs leaching. Leaching of Cs was dominantly controlled by diffusion from the pore space of the cement specimen to the solution. The effective diffusion coefficient and leachability index of nuclide were determined using the diffusion-release models of ANS 16.1. The results of present study can be used in the safety assessment for disposal of the radioactive waste generated by decommissioning of nuclear power plants.

An accumulation of spent nuclear fuel (SNF) has brought a considerable interest due to its energy and environmental issue. To effectively manage SNF, a pyroprocessing is introduced to separate useful resources from the spent fuels and to manufacture suitable fuels. In head-end process of pyroprocessing, spent fuels are thermally treated to prepare UO2 pellets, where various radioactive gases from SNFs are released during thermal treatment. Within these gases, C-14 as CO2 form is a radioactive fission product which had a long half-life of 5,730 years and emits beta radiation of 0.156 MeV. Generally, current CO2 capturing technologies include adsorption by solid materials, absorption by aqueous solutions, and membrane separation. Among these methods, absorption is an effective approach which traps CO2 effectively and and it is easy to operate at room temperature. In addition, it is highly recommended as immobilizing 14CO2 as CaCO3 formation due to the high thermal and chemical stability, and the relatively low solubility in water. Generally, a double alkali method has been proposed to capture low concentrated 14CO2 from the stream. This method for CO2 capture includes absorption process with NaOH solution and causticization using Ca(OH)2. In this study, CO2 emitted from SNF is captured using double alkali method, and the effects of operating conditions on capturing efficiency were investigated. Furthermore, considering the two-film theory, the effects of trapping conditions on the CO2 absorption performance were examined. The recovered CaCO3 from causticization was collected from the absorbing solution and analyzed.

The capacity of high nickel Li(NixCoyMn1-x-y)O2 (NCM, x ≥ 0.8) cathodes is known to rapidly decline, a serious problem that needs to be solved in a timely manner. It was reported that cathode materials with the {010} plane exposed toward the outside, i.e., a radial structure, can provide facile Li+ diffusion paths and stress buffer during repeated cycles. In addition, cathodes with a core-shell composition gradient are of great interest. For example, a stable surface structure can be achieved using relatively low nickel content on the surface. In this study, precursors of the high-nickel NCM were synthesized by coprecipitation in ambient atmosphere. Then, a transition metal solution for coprecipitation was replaced with a low nickel content and the coprecipitation reaction proceeded for the desired time. The electrochemical analysis of the core-shell cathode showed a capacity retention of 94 % after 100 cycles, compared to the initial discharge capacity of 184.74 mA h/g. The rate capability test also confirmed that the core-shell cathode had enhanced kinetics during charging and discharging at 1 A/g.

Extensive research is being carried out on Ni-rich Li(NixCoyMn1-x-y)O2 (NCM) due to the growing demand for electric vehicles and reduced cost. In particular, Ni-rich Li(NixCoyMn1-x-y-zAlz)O2 (NCMA) is attracting great attention as a promising candidate for the rapid development of Co-free but electrochemically more stable cathodes. Al, an inactive element in the structure, helps to improve structural stability and is also used as a doping element to improve cycle capability in Ni-rich NCM. In this study, NCMA was successfully synthesized with the desired composition by direct coprecipitation. Boron and tin were also used as dopants to improve the battery performance. Macro- and microstructures in the cathodes were examined by microscopy and X-ray diffraction. While Sn was not successfully doped into NCMA, boron could be doped into NCMA, leading to changes in its physicochemical properties. NCMA doped with boron revealed substantially improved electrochemical properties in terms of capacity retention and rate capability compared to the undoped NCMA.