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铬在希腊含水层中的来源和浓度分布。

Origin and concentration profile of chromium in a Greek aquifer.

机构信息

School of Civil Engineering, Department of Water Resources and Environmental Engineering, National Technical University of Athens, Iroon Polytechniou 9, 157 80 Zografou, Greece.

School of Civil Engineering, Department of Water Resources and Environmental Engineering, National Technical University of Athens, Iroon Polytechniou 9, 157 80 Zografou, Greece.

出版信息

J Hazard Mater. 2015 Jan 8;281:35-46. doi: 10.1016/j.jhazmat.2014.09.050. Epub 2014 Oct 2.

Abstract

In this paper the origin and concentration of chromium (Cr) in an ophiolitic aquifer in Vergina, northern Greece were investigated. The study area has only agricultural activity so that industrial Cr contamination was precluded. Soil sampling included topsoil and drillcore samples collected down to 98 m depth. Groundwater samples were collected from three existing wells and a spring at the area and from different depths of the soil boring using the discrete sampling method. Mineralogical analysis of soils confirmed the presence of ultramafic minerals, including chrysotile and chromite. Soil elemental analysis showed significant concentration of total chromium (Crtot; max 12,000 mg/kg) and hexavalent chromium (Cr(VI); max 7.5mg/kg). Significant Crtot (91 μg/L) and Cr(VI) (64 μg/L) concentrations exceeding the drinking water limit of 50 μg/L were also detected in groundwater. In both the discrete soil and groundwater samples a decreasing trend of Cr(VI) concentration was observed with increasing depth, while Crtot increased. The increasing trend in Crtot is attributed to the increasing contribution of unweathered ultramafic minerals with depth, while the decreasing Cr(VI) may be related to the increasing soil pH that does not favor Cr(III) oxidation by Mn-oxides.

摘要

本文研究了希腊北部 Vergina 蛇绿岩含水层中铬(Cr)的来源和浓度。研究区域仅开展农业活动,因此排除了工业 Cr 污染的可能性。土壤采样包括采集至 98 米深度的表土和岩芯样本。地下水样本取自该地区现有的三口井和一处泉水,以及土壤钻孔的不同深度,采用离散采样法采集。土壤矿物学分析证实存在超镁铁质矿物,包括纤蛇纹石和铬铁矿。土壤元素分析显示总铬(Crtot;最高 12000mg/kg)和六价铬(Cr(VI);最高 7.5mg/kg)浓度显著升高。地下水中 Crtot(91μg/L)和 Cr(VI)(64μg/L)浓度也超过饮用水限值 50μg/L。在离散的土壤和地下水样本中,Cr(VI)浓度随深度增加呈下降趋势,而 Crtot 则增加。Crtot 的增加趋势归因于未风化的超镁铁质矿物随深度增加而增加,而 Cr(VI)的减少可能与土壤 pH 值增加有关,这不利于 Mn 氧化物氧化 Cr(III)。

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