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首页> 外文期刊>Applied Geochemistry: Journal of the International Association of Geochemistry and Cosmochemistry >Distribution and origin of major and trace elements (particularly REE, U and Th) into labile and residual phases in an acid soil profile (Vosges Mountains, France)
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Distribution and origin of major and trace elements (particularly REE, U and Th) into labile and residual phases in an acid soil profile (Vosges Mountains, France)

机译:在酸性土壤剖面中主要和微量元素(尤其是REE,U和Th)的不稳定相和残留相的分布和起源(法国,孚日山脉)

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摘要

A 7 step sequential extraction procedure has been conducted on a podzolic soil profile from the Vosges Mountains in order to determine the ability of several elements to be released to the environment. Very little Si, K and Al were extractable (< 10% of the total soil concentration) but larger proportions (> 10% of the total soil concentration) of Ca, P, metals (Fe, Pb), REE and actinides (Th, U) could be leached. For each element, preferential binding sites can be recognized. High recovery of P and Ca in the acid soluble fraction (AS) suggests that phosphate minerals are highly involved in this step of the extraction. Organic matter appears to control the adsorption of Ca, Fe, Th, U and REE, even at depths in the soil profile where organic matter content is particularly low (0.5%). Weak acid leaching experiments (with HCl and acetic acid 0.001 N) were also performed in order to characterize the origin of the insoluble material in this soil profile. The leachable REE distributions indicate that a large part of the labile REE in the surface horizon has an atmospheric origin whereas at greater depth phosphate mineral (apatite) alteration is the main factor controlling REE release in the leachate. The study further suggests that adsorbed material holding actinides and REE are not strictly the same. So, caution should be taken when using REE as analogues for actinides in soils systems. (C) 2003 Elsevier Ltd. All rights reserved.
机译:为了确定几种元素释放到环境中的能力,已经对孚日山脉的坡地土壤剖面进行了7步连续提取程序。可提取的硅,钾和铝极少(<占土壤总浓度的10%),但钙,磷,金属(铁,铅),稀土元素和act系元素(Th, U)可能被浸出。对于每个元素,可以识别优先结合位点。酸溶级分(AS)中P和Ca的高回收率表明,磷酸盐矿物质与萃取的这一步骤高度相关。即使在土壤剖面中有机物含量特别低(0.5%)的深度,有机物似乎也能控制Ca,Fe,Th,U和REE的吸附。还进行了弱酸浸提实验(使用HCl和0.001 N的乙酸),以表征这种土壤剖面中不溶物的来源。可浸出的稀土元素分布表明,表层中大部分不稳定的稀土元素都来自大气,而在更深的深度,磷酸盐矿物(磷灰石)的变化是控制渗滤液中稀土元素释放的主要因素。研究进一步表明,吸附有act系元素和REE的物质并不完全相同。因此,在土壤系统中使用稀土元素作为act系元素的类似物时应格外小心。 (C)2003 Elsevier Ltd.保留所有权利。

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