首页> 外文期刊>Soil Science and Plant Nutrition >The distribution coefficient for cesium in different clay fractions in soils developed from granite and Paleozoic shales in Japan.
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The distribution coefficient for cesium in different clay fractions in soils developed from granite and Paleozoic shales in Japan.

机译:在日本花岗岩和古生代页岩发育的土壤中,铯在不同粘土组分中的分布系数。

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摘要

The distribution coefficient of cesium (Cs) (KdCs) was investigated for clays which were collected from upland forest soils developed from granites and Paleozoic shales in Japan. They were divided into three size fractions, coarse (2.0-1.0 micro m), medium (1.0-0.2 micro m), and fine-clay fractions (<0.2 micro m), abbreviated CC, MC, and FC, respectively. The KdCs value increased in the fractions as follows: FC < MC < CC in all the horizon samples. The amount of potassium (K) in the clay fractions also followed this same pattern. As the amount of K in the clay fraction can be a quantitative indicator of illitic minerals, the positive relationship between the KdCs and the amount of K indicated that the coarser clay fraction had a higher 137Cs adsorption potential due to containing higher amounts of illitic minerals. The soil clay fraction from the Paleozoic shales both contained a large amount of K and showed greater KdCs values than that of the granite when comparing the same particle sizes. Hence, the type of parent material can be a significant factor in determining the 137Cs adsorption potential of the soils. In all particle fractions, those collected from deeper in the profile had smaller KdCs values than those from closer to the soil surface in the same profile, although amount of K present was similar. The X-ray diffraction (XRD) analysis showed that the hydroxy-aluminum (Al) polymer was present in the 2:1 interlayer sites to a greater extent in the clay fractions from deeper in the soil profile than in those from upper in the same soil profile. This result suggests that the hydroxy-Al polymers may be fixed at the expanded weathering front of the illitic minerals, blocking Cs adsorption on the frayed edge sites of these minerals. Thus, the KdCs value of the soil clays is determined by the degree of illitic minerals and hydroxy-Al interlayering present, with the larger the amount of illitic minerals the greater the Cs adsorption potential (with any hydroxy-Al interlayering reducing this effect).
机译:研究了从日本花岗岩和古生代页岩发育的山地森林土壤中收集的粘土中铯(Cs)(Kd Cs )的分配系数。它们分为三个尺寸部分,分别为粗颗粒(2.0-1.0微米),中等颗粒(1.0-0.2微米)和细粘土部分(<0.2微米),缩写为CC,MC和FC。 Kd Cs 值按以下比例增加:在所有层位样本中,FC 与K含量之间呈正相关关系,表明较粗的粘土组分具有较高的 137 Cs的吸附潜力,因为其中包含大量的非法矿物。比较相同粒度时,古生代页岩中的土壤黏土部分都含有大量的K,并且比花岗岩中的Kd Cs 值更大。因此,母体材料的类型可能是决定土壤 137 Cs吸附潜力的重要因素。在所有颗粒级分中,尽管存在的K量相似,但从更深的剖面中收集的那些Kd Cs 值要比从更接近土壤表面的剖面中的Kd Cs 值小。 X射线衍射(XRD)分析表明,在土壤剖面较深处的粘土级分中,羟基铝(Al)聚合物在2:1中间层位点存在的程度要高于相同位置的上部土壤中的含量。土壤剖面。该结果表明,羟基-Al聚合物可以固定在硅质矿物的扩展的风化前沿,从而阻止Cs吸附在这些矿物的磨损边缘部位。因此,土壤黏土的Kd Cs 值由存在的非法矿物和羟基-铝中间层的程度决定,非法矿物的含量越大,Cs的吸附潜力就越大(任何羟基-铝中间层减少了这种影响)。

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