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Nakasone, Shunya*; Yokoyama, Sumi*; Takahashi, Tomoyuki*; Ota, Masakazu; Kakiuchi, Hideki*; Sugihara, Shinji*; Hirao, Shigekazu*; Momoshima, Noriyuki*; Tamari, Toshiya*; Shima, Nagayoshi*; et al.
Plasma and Fusion Research (Internet), 16, p.2405035_1 - 2405035_5, 2021/02
Removal of impurities such as organic and other types of dissolved matters from environmental water samples is required for precise analysis of tritium with a liquid scintillation counting method. In general, a distillation method is a conventional one for tritium analysis in environmental water samples, but is a time-consuming process that takes 24 hours for removal of impurities. We have proposed a rapid pretreatment method for tritium analysis, that uses ion exchange resins. In this study, we performed batch experiments, to evaluate the effectiveness of the ion exchange resins on the tritium measurement. The results obtained demonstrated that removal of impurities in the sample water by ion exchange resins can be achieved during a short period of time (i.e., in 5 min).
Nakasone, Shunya*; Yokoyama, Sumi*; Takahashi, Tomoyuki*; Ota, Masakazu; Kakiuchi, Hideki*; Sugihara, Shinji*; Hirao, Shigekazu*; Momoshima, Noriyuki*; Tamari, Toshiya*; Shima, Nagayoshi*; et al.
Plasma and Fusion Research (Internet), 15, p.2405027_1 - 2405027_3, 2020/05
A quick preprocessing system for tritium analysis of environmental samples is important to judge environmental influence of tritium releases due to accident or tritium-handling facilities. Analysis of tritium in water samples with liquid scintillation counting method requires removal of impurities such as organic matter and ion species from water samples. Generally, a distillation method is adopted as a pretreatment of analysis for tritium; however, the distillation method is a time-consuming process. The aim of this study is to evaluate a rapid pretreatment method for tritium analysis with ion exchange resin. From batch and column experiments that used inland water and ion exchange resin, we confirmed removals of impurities of the water sample and that the removal of impurities was possible for a short time (by 5 minutes).
Yokoyama, Sumi*; Takahashi, Tomoyuki*; Ota, Masakazu; Kakiuchi, Hideki*; Sugihara, Shinji*; Hirao, Shigekazu*; Momoshima, Noriyuki*; Tamari, Toshiya*; Shima, Nagayoshi*; Atarashi-Andoh, Mariko; et al.
Plasma and Fusion Research (Internet), 14(Sp.2), p.3405099_1 - 3405099_4, 2019/06
The Large Helical Device of the National Institute for Fusion Science started D-D experiments in 2017. To ensure the safety of the facility, it is important to develop evaluation methods for environmental tritium transfer. Tritiated water (HTO) in atmosphere and soil is transferred to plants, and organically bound tritium (OBT) is formed by photosynthesis. Prediction of OBT formation is important, because OBT accumulates in plants and causes dose through ingestion. The objective of this study is to estimate environmental tritium transfer using a simple compartment model and practical parameters. We proposed a simple compartment model consisting of air-soil-plant components, and tried to validate the model by comparison with a sophisticated model, SOLVEG. In this study, we plan to add wet deposition to the model and obtain parameters from measurements of soil permeability and tritium concentrations in air, soil and plants. We also establish rapid pretreatment methods for OBT analysis.
Sugihara, Shinji*; Tanaka, Masahiro*; Tamari, Toshiya*; Shimada, Jun*; Takahashi, Tomoyuki*; Momoshima, Noriyuki*; Fukutani, Satoshi*; Atarashi-Andoh, Mariko; Sakuma, Yoichi*; Yokoyama, Sumi*; et al.
Fusion Science and Technology, 60(4), p.1300 - 1303, 2011/11
Times Cited Count：2 Percentile：18.92(Nuclear Science & Technology)The purpose of this study is to develop the technique to evaluate the environmental tritium behavior of the nuclear facility origin. Tritium concentrations of river water, precipitation and ground water around the NIFS site were determined by low background liquid scintillation measurement system combined with the electrolysis using solid polymer electrolyte. The electric conductivity and flow rate of the river and isotopic ratio of oxygen and hydrogen of water samples were also measured. The tritium concentrations in precipitation showed the seasonal variation and the range were 0.09-0.78 Bq/L. The tritium concentrations of river water and ground water were almost constant, 0.34 and 0.24 Bq/L respectively. The simple dynamic model for the site around the NIFS facilities was developed using measured data, and the behavior of tritium was simulated.
Yokoyama, Sumi*; Takahashi, Tomoyuki*; Ota, Masakazu; Kakiuchi, Hideki*; Sugihara, Shinji*; Hirao, Shigekazu*; Momoshima, Noriyuki*; Tamari, Toshiya*; Shima, Nagayoshi*; Atarashi-Andoh, Mariko; et al.
no journal, ,
To ensure safety of fusion facilities, it is important to develop evaluation methods for tritium transfer in the environment. For estimation of tritium transfer in the terrestrial environment, we had developed a simple compartment model using the Migration Of GRound Additions (MOGRA) code. The model was composed by an air-soil-plant system. The target source terms were HT and HTO in the air. In addition, wet deposition was modeled by input of HTO to the system by rainfall. Tritium in the plant was divided into free water tritium (FWT) and organically bound tritium (OBT). The tritium concentration in the environmental medium was trial calculated for chronic and accidental HTO releases to the atmosphere, as preliminary calculation run of the model.
Kakiuchi, Hideki*; Tanaka, Masahiro*; Fukutani, Satoshi*; Sugihara, Shinji*; Hirao, Shigekazu*; Momoshima, Noriyuki*; Tamari, Toshiya*; Shima, Nagayoshi*; Atarashi-Andoh, Mariko; Furukawa, Masahide*; et al.
no journal, ,
no abstracts in English
