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地下水钒的区域分布控制因素。

Factors controlling the regional distribution of vanadium in groundwater.

机构信息

U.S. Geological Survey, California Water Science Center, San Diego, CA 92101, USA.

出版信息

Ground Water. 2010 Jul-Aug;48(4):515-25. doi: 10.1111/j.1745-6584.2009.00666.x. Epub 2010 Jan 20.

DOI:10.1111/j.1745-6584.2009.00666.x
PMID:20100292
Abstract

Although the ingestion of vanadium (V) in drinking water may have possible adverse health effects, there have been relatively few studies of V in groundwater. Given the importance of groundwater as a source of drinking water in many areas of the world, this study examines the potential sources and geochemical processes that control the distribution of V in groundwater on a regional scale. Potential sources of V to groundwater include dissolution of V rich rocks, and waste streams from industrial processes. Geochemical processes such as adsorption/desorption, precipitation/dissolution, and chemical transformations control V concentrations in groundwater. Based on thermodynamic data and laboratory studies, V concentrations are expected to be highest in samples collected from oxic and alkaline groundwater. However, the extent to which thermodynamic data and laboratory results apply to the actual distribution of V in groundwater is not well understood. More than 8400 groundwater samples collected in California were used in this study. Of these samples, high (> or =50 microg/L) and moderate (25 to 49 microg/L) V concentrations were most frequently detected in regions where both source rock and favorable geochemical conditions occurred. The distribution of V concentrations in groundwater samples suggests that significant sources of V are mafic and andesitic rock. Anthropogenic activities do not appear to be a significant contributor of V to groundwater in this study. High V concentrations in groundwater samples analyzed in this study were almost always associated with oxic and alkaline groundwater conditions, which is consistent with predictions based on thermodynamic data.

摘要

虽然饮用水中摄入钒(V)可能会对健康产生不利影响,但关于地下水中钒的研究相对较少。鉴于地下水作为世界许多地区饮用水源的重要性,本研究考察了控制地下水中钒分布的潜在来源和地球化学过程。地下水的潜在钒源包括富含钒的岩石的溶解,以及工业过程的废水。吸附/解吸、沉淀/溶解和化学转化等地球化学过程控制着地下水中钒的浓度。基于热力学数据和实验室研究,预计在有氧和碱性地下水采集的样本中 V 浓度最高。然而,热力学数据和实验室结果对实际地下水中 V 分布的适用程度还不是很清楚。本研究共使用了加利福尼亚州采集的 8400 多个地下水样本。在这些样本中,高(>=50μg/L)和中(25 至 49μg/L)浓度 V 最常出现在源岩和有利地球化学条件同时存在的地区。地下水样本中 V 浓度的分布表明,V 的重要来源是基性和安山岩。在本研究中,人为活动似乎不是地下水 V 的重要来源。本研究分析的地下水样本中高浓度 V 几乎总是与有氧和碱性地下水条件有关,这与基于热力学数据的预测一致。

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