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河水悬浮颗粒物中放射性铯在海水中的解吸作用。

Desorption of radioactive cesium by seawater from the suspended particles in river water.

机构信息

Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 1-1 Katahira, 2-chome, Aoba-ku, Sendai 980-8577, Japan.

Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 1-1 Katahira, 2-chome, Aoba-ku, Sendai 980-8577, Japan.

出版信息

Chemosphere. 2017 Oct;185:806-815. doi: 10.1016/j.chemosphere.2017.07.078. Epub 2017 Jul 17.

Abstract

In 2011, the accident at the Fukushima-Daiichi nuclear power plant dispersed radioactive cesium throughout the environment, contaminating the land, rivers, and sea. Suspended particles containing clay minerals are the transportation medium for radioactive cesium from rivers to the ocean because cesium is strongly adsorbed between the layers of clay minerals, forming inner sphere complexes. In this study, the adsorption and desorption behaviors of radioactive cesium from suspended clay particles in river water have been investigated. The radioactive cesium adsorption and desorption experiments were performed with two kinds of suspended particulate using a batch method with Cs tracers. In the cesium adsorption treatment performed before the desorption experiments, simulated river water having a total cesium concentration ([Cs]) of 1.3 nM (10 mol/L) was used. The desorption experiments were mainly conducted at a solid-to-liquid ratio of 0.17 g/L. The desorption agents were natural seawater collected at 10 km north of the Fukushima-Daiichi nuclear power plant, artificial seawater, solutions of NaCl, KCl, NHCl, and CsCl, and ultrapure water. The desorption behavior, which depends on the preloaded cesium concentration in the suspended particles, was also investigated. Based on the cesium desorption experiments using suspended particles, which contained about 1000 ng/g loaded cesium, the order of cesium desorption ratios for each desorption agent was determined as 1 M NaCl (80%) > 470 mM NaCl (65%) > 1 M KCl (30%) ≈ seawater (natural seawater and Daigo artificial seawater) > 1 M NHCl (20%) > 1 M CsCl (15%) ≫ ultrapure water (2%). Moreover, an interesting result was obtained: The desorption ratio in the 470 mM NaCl solution was much higher than that in seawater, even though the Na concentrations were identical. These results indicate that the cesium desorption mechanism is not a simple ion exchange reaction but is strongly related to structural changes in the clay minerals in the suspended particles. Hydrated Na ions expand the interlayer distance of the clay minerals, resulting in the facile desorption of cesium; in contrast, dehydrated K ions reduce the interlayer distance and inhibit the desorption of cesium. In conclusion, the desorption of cesium from the suspended particles is controlled by the presence of sodium and potassium ions and the preloaded cesium concentration in the suspended particles.

摘要

2011 年,福岛第一核电站事故使放射性铯散布到环境中,污染了土地、河流和海洋。含有粘土矿物的悬浮颗粒是河流中放射性铯向海洋输送的媒介,因为铯强烈吸附在粘土矿物的层间,形成内球络合物。在这项研究中,研究了河水中悬浮粘土颗粒中放射性铯的吸附和解吸行为。采用 Cs 示踪剂的批量法进行了两种悬浮颗粒的放射性铯吸附和解吸实验。在解吸实验之前进行的铯吸附处理中,使用了总铯浓度([Cs])为 1.3 nM(10 mol/L)的模拟河水。解吸实验主要在固液比为 0.17 g/L 的条件下进行。解吸剂为福岛第一核电站以北 10 公里处采集的天然海水、人工海水、NaCl、KCl、NH4Cl 和 CsCl 溶液以及超纯水。还研究了依赖于悬浮颗粒中预加载铯浓度的解吸行为。基于含有约 1000ng/g 加载铯的悬浮颗粒的铯解吸实验,确定了每种解吸剂的铯解吸率顺序为 1M NaCl(80%)>470mM NaCl(65%)>1M KCl(30%)≈海水(天然海水和大海人工海水)>1M NH4Cl(20%)>1M CsCl(15%)>>超纯水(2%)。此外,得到了一个有趣的结果:尽管 Na 浓度相同,但 470mM NaCl 溶液中的解吸率远高于海水。这些结果表明,铯的解吸机制不是简单的离子交换反应,而是与悬浮颗粒中粘土矿物的结构变化密切相关。水合 Na 离子扩展了粘土矿物的层间距,导致铯的易解吸;相反,脱水 K 离子减小了层间距,抑制了铯的解吸。总之,悬浮颗粒中铯的解吸受钠离子和钾离子的存在以及悬浮颗粒中预加载铯浓度的控制。

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