Pre-enrichment of radioactive cesium in muddy water separated into suspended and dissolved substances for trace analysis.

A new in-situ pre-enrichment system was developed for trace analysis of radioactive Cs in environmental water such as rivers, ponds, and seas, where the radioactive Cs is separated into suspended substances (SS) and dissolved substances (DS). The SS component was collected as the enrichment slurry by cross-flow filtration, thereby compact systems were realized. The DS component was collected in a small cartridge filled with a non-woven fiber with immobilized adsorbent nanoparticles. The recovery rate was estimated at around 95%. The size distribution of the SS and the concentration of radioactive Cs after enrichment were the same as that of the raw water before enrichment. The condensed SS can be used for other evaluations such as ignition loss. From the field test at a pond in the Fukushima-area, the Cs concentration of the SS was found to be 4-5 times higher than that of the sediment in the same pond. The organic content estimated by ignition loss was also three times higher.

Inversion analysis on vertical radiocesium distribution in pond sediment from γ-ray count measurement.

Evaluation of vertical distribution of radiocesium in bottom sediment by measuring vertical γ-ray count profile was discussed. A stable inversion formula was derived based on the maximum entropy method. Efficiency of the formula was confirmed by using a low-cost apparatus composed of an array of PIN photodiodes and a single board computer with real-time inversion code. In-door experiment by using five model sediment disks showed good reproducibility of vertical radiocesium profile. On-site experiment was also carried out at a pond in Fukushima to confirm the efficiency. It was suggested that combination of the simple apparatus and MEM inversion formula gave reasonable estimates on vertical radiocesium distribution in bottom sediment of 1 kBq/kg-wet level within about 10 min.

Radiocesium removal system for environmental water and drainage.

With the development of the nuclear power generation, it is expected that severe pollution of environmental water by radiocesium (r-Cs) may occur. We developed a r-Cs removal system with a continuous stirring tank reactor (CSTR) and r-Cs adsorbent of non-woven fiber immobilizing Prussian blue nanoparticles (PBN). Results confirmed that this system can remove r-Cs from environmental water with a removal rate higher than 80% at processing speed of 2 m3/h. In this study, the processing speed and processing capacity of this system were confirmed using kinetic and equilibrium analyses of Cs adsorption behavior on PBN. The equilibrium of Cs adsorption was analyzed using a Langmuir equation. Results show that the maximum adsorption capacity was 160 mg/g (PBN). The kinetic data were well fitted using a pseudo-first order kinetic model. This rate constant was correlated to the PBN/liquid ratio in the system.

Variation in available cesium concentration with parameters during temperature induced extraction of cesium from soil.

Cesium extraction behavior of brown forest type soil collected from paddy fields in Fukushima nuclear accident affected areas was studied. In nitric acid or sulfuric acid solutions at elevated temperature, the concentration of Cs in soil available for extraction, m0, has been estimated on the basis of modified canonical equation and the equations derived from assumed equilibria. With the variation in temperature, mixing time, and soil to solvent ratio, the observed m0 values in 0.5 M acid solution ranged between 1.5 and 2.9 mg cesium per kilogram of soil. By increasing the acid concentration to 3 M, the value of m0 could be sharply increased to 5.1 mg/kg even at 95 °C. This variation in the extractable concentration of cesium with the parameters signifies the existence of different binding sites in the soil matrix. The results observed for uncontaminated sample could be reproduced with the radioactive cesium contaminated sample belonging to the same soil group.

Dealing with the aftermath of Fukushima Daiichi nuclear accident: decontamination of radioactive cesium enriched ash.

Environmental radioactivity, mainly in the Tohoku and Kanto areas, due to the long living radioisotopes of cesium is an obstacle to speedy recovery from the impacts of the Fukushima Daiichi Nuclear Power Plant accident. Although incineration of the contaminated wastes is encouraged, safe disposal of the Cs enriched ash is the big challenge. To address this issue, safe incineration of contaminated wastes while restricting the release of volatile Cs to the atmosphere was studied. Detailed study on effective removal of Cs from ash samples generated from wood bark, household garbage, and municipal sewage sludge was performed. For wood ash and garbage ash, washing only with water at ambient conditions removed radioactivity due to (134)Cs and (137)Cs, retaining most of the components other than the alkali metals with the residue. However, removing Cs from sludge ash needed acid treatment at high temperature. This difference in Cs solubility is due to the presence of soil particle originated clay minerals in the sludge ash. Because only removing the contaminated vegetation is found to sharply decrease the environmental radioactivity, volume reduction of contaminated biomass by incineration makes great sense. In addition, need for a long-term leachate monitoring system in the landfill can be avoided by washing the ash with water. Once the Cs in solids is extracted to the solution, it can be loaded to Cs selective adsorbents such as Prussian blue and safely stored in a small volume.

Male chromosomes of sea urchin hybrid andromerogones created with cryopreserved sperm.

We developed a method for preparing male chromosomes from sea urchin hybrid andromerogones created with cryopreserved sperm. We obtained hybrid andromerogones by heterospermic insemination of Hemicentrotus pulcherrimus non-nucleate egg fragments produced by centrifuging unfertilized eggs in a stepwise saccharose density gradient. The hybrid andromerogones showed cleavage rates of 1%-93%, cleaved successively into two- and four- blastomeres and developed to early blastulae. The morulae or early blastulae were treated with colchicine (0.1-1.0 mg/ml), dissociated into single blastomeres by pippeting, swollen with 7%-10% sodium citrate for 10 min and fixed with methanol:acetic acid (3:1). The fixed cells were dropped on slides and air-dried. The andromerogones for 5 sperm species showed a half of their respective diploid chromosome numbers without chromosome elimination. This method is applicable for analysis of the haploid male chromosome complement in sea urchin species for which only sperm can be obtained.