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首页> 外文期刊>Applied Geochemistry: Journal of the International Association of Geochemistry and Cosmochemistry >Sulfur isotope studies to quantify sulfate components in water of flooded lignite open pits - Lake Goitsche, Germany
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Sulfur isotope studies to quantify sulfate components in water of flooded lignite open pits - Lake Goitsche, Germany

机译:硫同位素研究以定量淹没褐煤露天矿井水中的硫酸盐成分-德国戈采湖

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摘要

A system of connected lignite mining pits (part of the former Goitsche mining complex, Germany) was flooded with river water between 1999 and 2002. A considerable accumulation of acid associated with oxidized sulfides in sediments was seen as a critical point for the development of the lake water. To characterize the components contributing to the supply of dissolved lake water SO4 hydro-chemical and isotope investigations with respect to groundwater, pore water in the sulfide bearing sediments, river water and lake water were performed. delta S-34 of pore water SO4 that was dominated by oxidized pyrites ranges around -25 parts per thousand. VCDT and differs strongly from river water SO4 with about +4.4 parts per thousand. Thus, interactions between lake water and sediments were particularly pronounced during the first phase of flooding. For this period, a more quantitative estimation of the SO4 components in the lake water was difficult because of the heterogeneous SO4 distributions between the different sub-basins of the lake and according to the flooding process itself. Later, a component separation was attempted following mixing of the whole lake, which first occurred in spring 2002. A very heterogeneous groundwater environment with respect to highly variable SO4 concentrations and delta S-34 values and changing interaction with the forming lakes proved to be one of the most important limitations in the calculations of the mixing. (c) 2006 Elsevier Ltd. All rights reserved.
机译:在1999年至2002年之间,相连的褐煤矿坑系统(德国前Goitsche矿区的一部分)被河水淹没。沉积物中大量与氧化硫化物相关的酸积累被视为该矿床发展的关键点。湖水。为了表征有助于溶解的湖水供应的成分,对地下水,硫化物沉积物中的孔隙水,河水和湖水进行了SO4水化学和同位素研究。孔隙水SO4的δS-34值(被氧化的黄铁矿占主导)范围约为每千分之-25。 VCDT与水中SO4的差别很大,约为千分之4.4。因此,在洪水的第一阶段,湖水和沉积物之间的相互作用特别明显。在此期间,由于湖泊不同子流域之间以及洪水过程本身的SO4分布不均,很难对湖泊水中的SO4成分进行更定量的估算。后来,在整个湖水混合之后尝试进行组分分离,这首先发生在2002年春季。关于高度可变的SO4浓度和δ-S-34值以及与形成的湖水相互作用的变化,非常不均匀的地下水环境被证明是一个原因。混合计算中最重要的限制。 (c)2006 Elsevier Ltd.保留所有权利。

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