Nagao Seiya, Terasaki Soichiro, Ochiai Shinya, Fukushi Keisuke, Tomihara Seiichi, Charette Mathew A, Buesseler Ken O
Institute of Nature and Environmental Technology, Kanazawa University, Kakuma, Kanazawa, Ishikawa, 920-1192, Japan.
Graduate School of Natural Science and Engineering, Kanazawa University, Kakuma, Kanazawa, Ishikawa, 920-1192, Japan.
Anal Sci. 2020;36(5):569-573. doi: 10.2116/analsci.19SBP08.
Beach sand samples were collected along a coastal area 32 km south of the Fukushima Daiichi Nuclear Power Plant (FDNPP) in Fukushima Prefecture, Japan, 5 years after the FDNPP accident. Desorption experiments were performed on the sand samples using seawater in a batch experimental system to understand the forms of existence of radiocesium in sand and their desorption behavior in a coastal environment. The percentage of radiocesium desorption decreased exponentially with an increase in the number of desorption experiments for the four sand samples, with Cs radioactivity from 16 to 1077 Bq kg at surface and deeper layers from three sites. Total desorption percentage ranged from 19 to 58% in 12 desorption experiments. The results indicate that the weak adsorption varies with the sampling sites and their depth layer. To understand the desorption behavior of radiocesium in the sand samples, the desorption experiments were performed for a sand sample by using natural and artificial seawater, and NaCl solution in the presence and absence of KCl. The Cs desorption from the sand collected at a depth of 100 - 105 cm from the ground surface (Cs radioactivity 1052 ± 25 Bq kg) was 0.1% by ultrapure water, 3.7% by 1/4 seawater and 7.1% by 1/2 seawater, 2.2% by 470 mM NaCl solution (corresponding to a similar concentration of seawater) and 10 - 12% by seawater, artificial seawater and 470 mM NaCl + 8 mM KCl solution. These results indicate that about 10% of radiocesium adsorbed on the sand is mainly desorbed by ion exchange of potassium ion in seawater, though the concentration of major cation, or sodium ion, in seawater makes a small contribution on Cs desorption from the sand samples.
在福岛第一核电站事故发生5年后,于日本福岛县福岛第一核电站以南32公里的沿海地区采集了海滩砂样。在间歇实验系统中,使用海水对砂样进行解吸实验,以了解砂中放射性铯的存在形式及其在沿海环境中的解吸行为。对于四个砂样,放射性铯的解吸百分比随着解吸实验次数的增加呈指数下降,三个地点表层和深层的铯放射性活度为16至1077 Bq/kg。在12次解吸实验中,总解吸百分比在19%至58%之间。结果表明,弱吸附随采样地点及其深度层而变化。为了解砂样中放射性铯的解吸行为,使用天然海水、人工海水以及存在和不存在氯化钾的氯化钠溶液对一个砂样进行了解吸实验。从距地面100 - 105厘米深处采集的砂样(铯放射性活度为1052 ± 25 Bq/kg),用超纯水解吸的铯为0.1%,用1/4海水为3.7%,用1/2海水为7.1%,用470 mM氯化钠溶液(相当于类似海水浓度)为2.2%,用海水、人工海水和470 mM氯化钠 + 8 mM氯化钾溶液为10 - 12%。这些结果表明,吸附在砂上的约10%的放射性铯主要通过海水中钾离子的离子交换解吸,尽管海水中主要阳离子(即钠离子)的浓度对砂样中铯的解吸贡献较小。