Flow filtration/adsorption and simultaneous monitoring technologies of radiocesium Cs in river water

Enomoto, Kazuyuki*; Hoshina, Hiroyuki*; Kasai, Noboru*; Kurita, Keisuke; Ueki, Yuji*; Nagao, Yuto*; Yin, Y.-G.*; Suzui, Nobuo*; Kawachi, Naoki*; Seko, Noriaki*

Chemical Engineering Journal, 460, p.141696_1 - 141696_9, 2023/03

https://doi.org/10.1016/j.cej.2023.141696

This study develops a method that combines a radiation-grafting fibrous Cs-adsorbent filter of ammonium molybdophosphate (AMP) and a Ce:GdAlGaO scintillator based -ray detector for in situ measurements of the activity concentrations of Cs in a continuous water flow.

A New approach to extracting biofilm from environmental plastics using ultrasound-assisted syringe treatment for isotopic analyses

Battulga, B.; Atarashi-Andoh, Mariko; Nakanishi, Takahiro; Koarashi, Jun

Science of the Total Environment, 849, p.157758_1 - 157758_11, 2022/11

https://doi.org/10.1016/j.scitotenv.2022.157758

Characterizing plastic-associated biofilms is key to the better understanding of organic material and mineral cycling in the "Plastisphere"-the thin layer of microbial life on plastics. In this study, we propose a new method to extract biofilms from environmental plastics, in order to evaluate the properties of biofilm-derived organic matter through stable carbon (C) and nitrogen (N) isotope signatures and their interactions with radionuclides especially radiocesium (Cs). After ultrasound-assisted separation from the plastics, biofilm samples were successfully collected via a sequence of syringe treatments. Biofilm-derived organic matter samples (14.5-65.4 mg) from four river mouths in Japan showed Cs activity concentrations of 75 to 820 Bq kg biofilm (dw), providing evidence that environmental plastics, mediated by developed biofilms, serve as a carrier for Cs in the coastal environment. Significant differences in the (C and N signatures were also obtained for the biofilms, indicating the different sources, pathways, and development processes of biofilms on plastics.

Toxicity reduction with total volume control in nuclear waste

Fukaya, Yuji; Ueta, Shohei; Yamamoto, Tomohiko; Chikazawa, Yoshitaka; Yan, X.

Nuclear Technology, 208(2), p.335 - 346, 2022/02

https://doi.org/10.1080/00295450.2021.1901001

When the total volume control on toxicity for nuclear waste management is applied, it becomes a limiting factor for the permittable total operation capacity of nuclear reactors. An alternative conceptual scenario to achieve the control is proposed that aims at toxicity reduction through Partitioning and Transmutation (P&T). Specifically, the electricity generation capacity could be inversely increased up with transmutation of Sr-Cs. Simultaneously, the cooling time before disposal is reduced to 50 years from the 300 years required by the existing scenarios such as (Accelerator Driven System (ADS). Finally, the scenario is also found feasible in terms of energy balance and cost by the neutron source of Li(d,xn) reaction with the deuteron accelerator for transmutation.

Determination of Cs/Cs isotopic ratio in soil collected near Fukushima Daiichi Nuclear Power Station through mass spectrometry

Shimada, Asako; Tsukahara, Takehiko*; Nomura, Masao*; Kim, M. S.*; Shimada, Taro; Takeda, Seiji; Yamaguchi, Tetsuji

Journal of Nuclear Science and Technology, 58(11), p.1184 - 1194, 2021/11

https://doi.org/10.1080/00223131.2021.1931520

Determining the completeness of nuclear reactor decommissioning is an important step in safely utilizing nuclear power. For example, Cs from the Fukushima Daiichi Nuclear Power Station (FDNPS) accident can be treated as background radioactivity, so determining the origin of Cs is essential. To accomplish this, measuring the Cs/Cs isotope ratio can be useful, so this study optimized a solvent extraction method, with calix[4]arene-bis(t-octylbenzo-crown-6) [BOBCalixC6] in 1-octanol, to purify radioactive Cs, radiocesium, from a solution of major environmental soil elements and mass spectrometry interference elements. This optimized method was applied to Cs purification in soil samples (40 g), and the final solutions contained a total of 10g/ml of the major soil elements and ng/ml concentrations at most of interfering elements. Soil samples collected near the FDNPS were then purified, and the Cs/Cs isotope ratios were measured, using both thermal ionization mass spectrometry (TIMS) and triple quadrupole induced coupled plasma mass spectrometry (ICP-QQQ). The results of each of these measurements were compared, and we found that Cs isotope ratios obtained by TIMS were more precise, by an order of magnitude, while the ICP-QQQ results possessed good abundance sensitivities. A slightly higher Cs/Cs ratio in the northwest area of the FDNPS was observed, while other areas exhibited similar values, all within the measurement error range, which indicated different origins of radiocesium. These results agreed with previously reported Cs/Cs activity distributions, suggesting that this ratio may be useful in identifying radiocesium origins for evaluating future nuclear reactor decommissions.

5.2.1 Models on radionuclides release from fuel under severe accident conditions, 5.4.5 Technical issues of current radionuclide behavior models obtained from the Fukushima accident analyses

Hidaka, Akihide

Fission Product Behavior under Severe Accident, p.85 - 88, 2021/05

no abstracts in English

A Model intercomparison of atmospheric Cs concentrations from the Fukushima Daiichi Nuclear Power Plant accident, phase III; Simulation with an identical source term and meteorological field at 1-km resolution

Sato, Yosuke*; Sekiyama, Tsuyoshi*; Fang, S.*; Kajino, Mizuo*; Qurel, A.*; Qulo, D.*; Kondo, Hiroaki*; Terada, Hiroaki; Kadowaki, Masanao; Takigawa, Masayuki*; et al.

Atmospheric Environment; X (Internet), 7, p.100086_1 - 100086_12, 2020/10

https://doi.org/10.1016/j.aeaoa.2020.100086

The third model intercomparison project for investigating the atmospheric behavior of Cs emitted during the Fukushima Daiichi Nuclear Power Plant (FDNPP) accident (FDNPP-MIP) was conducted. A finer horizontal grid spacing (1 km) was used than in the previous FDNPP-MIP. Nine of the models used in the previous FDNPP-MIP were also used, and all models used identical source terms and meteorological fields. Our analyses indicated that most of the observed high atmospheric Cs concentrations were well simulated, and the good performance of some models improved the performance of the multi-model ensemble. The analyses also confirmed that the use of a finer grid resolution resulted in the meteorological field near FDNPP being better reproduced. The good representation of the wind field resulted in the reasonable simulation of the narrow distribution of high deposition amount to the northwest of FDNPP and the reduction of the overestimation over the area to the south of FDNPP. In contrast, the performance of the models in simulating plumes observed over the Nakadori area, the northern part of Gunma, and the Tokyo metropolitan area was slightly worse.

Seven-year temporal variation of caesium-137 discharge inventory from the port of Fukushima Daiichi Nuclear Power Plant; Continuous monthly estimation of caesium-137 discharge in the period from April 2011 to June 2018

Machida, Masahiko; Yamada, Susumu; Iwata, Ayako; Otosaka, Shigeyoshi; Kobayashi, Takuya; Watanabe, Masahisa; Funasaka, Hideyuki; Morita, Takami*

Journal of Nuclear Science and Technology, 57(8), p.939 - 950, 2020/08

https://doi.org/10.1080/00223131.2020.1740809

After direct discharges of highly contaminated water of the Fukushima Daiichi Nuclear Power Plant (1F) from April to May 2011, Kanda suggested that relatively small amounts of run-off of radionuclides from the 1F port into the Fukushima coastal region subsequently continued by his estimation method. However, the estimation period was limited to up to September 2012. Therefore, this paper estimates the discharge inventory up to June 2018. In the missing period, the Japanese government and Tokyo Electric Power Company Holdings have continued efforts to stop the discharge, and consequently, the radionuclide concentration in seawater inside the 1F port has gradually diminished. We show the monthly discharge inventory of Cs up to June 2018 by two methods, i.e., Kanda method partially improved by the authors and a more sophisticated method using Voronoi tessellation reflecting the increase in the number of monitoring points inside the 1 F port. The results show that the former always yields overestimated results compared with the latter, but the ratio of the former to the latter is less than one order of magnitude. Using these results, we evaluate the impact of the discharge inventory from the 1F port into the coastal area and radiation dose upon fish ingestion.

Vertical and horizontal distributions of Cs on paved surfaces affected by the Fukushima Dai-ichi Nuclear Power Plant accident

Yoshimura, Kazuya; Watanabe, Takayoshi; Kurikami, Hiroshi

Journal of Environmental Radioactivity, 217, p.106213_1 - 106213_6, 2020/06

https://doi.org/10.1016/j.jenvrad.2020.106213

Direct quantitation of Cs in spent Cs adsorbent used for the decontamination of radiocesium-containing water by laser ablation inductively coupled plasma mass spectrometry

Asai, Shiho*; Ohata, Masaki*; Hanzawa, Yukiko; Horita, Takuma; Yomogida, Takumi; Kitatsuji, Yoshihiro

Analytical Chemistry, 92(4), p.3276 - 3284, 2020/02

https://doi.org/10.1021/acs.analchem.9b05161

The long-term safety assessment of spent Cs adsorbents produced during the decontamination of radiocesium-containing water at the Fukushima Daiichi Nuclear Power Plant requires one to estimate their Cs content prior to final disposal. Cs is usually quantified by inductively coupled plasma mass spectrometry (ICP-MS), which necessitates the elution of Cs from Cs adsorbents. However, this approach suffers from the high radiation dose from Cs. To address this challenge, we herein employed laser ablation ICP-MS for direct quantitation of Cs in Cs adsorbents and used a model Cs adsorbent prepared by immersion of a commercially available Cs adsorbent into radiocesium-containing liquid waste to verify the developed technique. The use of the Cs/Cs ratio and Cs radioactivity obtained by gamma spectrometry achieved simple and precise quantitation of Cs and the resulting Cs activity of 0.36 Bq agreed well with that in the original radiocesium-containing liquid waste.

Seven-year temporal variation of cesium-137 discharge inventory from the port of Fukushima Dai-ichi Nuclear Power Plant; Continuous monthly estimation of cesium-137 discharge in the period from April 2011 to June 2018

Machida, Masahiko; Yamada, Susumu; Iwata, Ayako; Otosaka, Shigeyoshi; Kobayashi, Takuya; Watanabe, Masahisa; Funasaka, Hideyuki; Morita, Takami*

Nihon Genshiryoku Gakkai Wabun Rombunshi, 18(4), p.226 - 236, 2019/12

https://doi.org/10.3327/taesj.J18.030

After direct discharges of highly-contaminated water from Unit 2 and 3 in Fukushima Daiichi Nuclear Power Plant (1F) in April to May 2011, Kanda suggested that relatively small run-off of radionuclides from 1F port into Fukushima coastal region has subsequently continued by using his estimation scheme. However, the estimation period was limited until September 2012, and there has been no report on the issue since the work. Therefore, this paper focuses on discharge inventory from 1F port until June 2018. In the missing period, the central government and Tokyo Electric Power Company Holdings have done continuous efforts to stop the discharge, and consequently sea water concentration inside 1F port has diminished gradually. We show monthly discharge inventory of Cs-137 until June 2018 by two schemes, i.e., Kanda's scheme partially improved by authors and more sophisticated one using Voronoi tessellation reflecting the increment of the number of monitoring points inside 1F port. The results show that the former always presents overestimated results compared to the latter but the ratio of former to latter is less than one order. Based on these results, we evaluate impact of discharge inventory from 1F port into the coastal area and radiation does via fish digestion.