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矿山尾矿在氧化还原活跃环境下:铁地球化学和潜在的环境影响。

Mine tailings in a redox-active environment: Iron geochemistry and potential environmental consequences.

机构信息

Department of Soil Science, "Luiz de Queiroz" College of Agriculture, University of São Paulo, Piracicaba, São Paulo, Brazil.

Department of Soil and Crop Sciences, Texas A&M University, College Station, TX, USA.

出版信息

Sci Total Environ. 2022 Feb 10;807(Pt 3):151050. doi: 10.1016/j.scitotenv.2021.151050. Epub 2021 Oct 19.

Abstract

Iron (Fe) oxyhydroxides provide many functions in soils, mainly owing to their large surface area and high surface charge density. The reactivity of Fe oxyhydroxides is function of their mineralogical characteristics (e.g., crystallinity degree and crystal size). Detailed studies of these features are essential for predicting the stability and reactivity of these minerals within soil and sediments. The present study aimed to evaluate geochemical changes in Fe-rich tailings after the world's largest mining disaster in SE Brazil (in 2015) and to predict the potential environmental implications for the estuary. The mineralogical characteristics of the tailings were studied at three different times (2015, 2107, and 2019) to assess how an active redox environment affects Fe oxyhydroxides and to estimate the time frame within which significant changes occur. The study findings indicate a large decrease in the Fe oxyhydroxides crystallinity, which were initially composed (93%) of highly crystalline Fe oxyhydroxides (i.e., goethite and hematite) and 6.7% of poorly crystalline Fe oxyhydroxides (i.e., lepidocrocite and ferrihydrite). Within 4 years the mineralogical features of Fe oxyhydroxides had shifted, and in 2019 poorly crystalline Fe oxyhydroxides represented 47% of the Fe forms. Scanning electron microscope micrographs and the mean crystal size evidenced a decrease in particle size from 109 nm to 49 nm for goethite in the d direction. The changes in mean crystal size increased the reactivity of Fe oxyhydroxides, resulting in a greater number of interactions with cationic and anionic species. The decreased crystallinity and increased reactivity led to the compounds being more susceptible to reductive dissolution. Overall, the findings show that the decrease in crystallinity along with higher susceptibility to reductive dissolution of Fe oxyhydroxides can affect the fate of environmentally detrimental elements (e.g., phosphorus and trace metals) thereby increasing the concentration of these pollutants in estuarine soils and waters.

摘要

铁(Fe)氢氧化物在土壤中提供了多种功能,主要归因于其较大的表面积和较高的表面电荷密度。Fe 氢氧化物的反应性取决于其矿物学特征(例如,结晶度和晶体尺寸)。详细研究这些特征对于预测这些矿物在土壤和沉积物中的稳定性和反应性至关重要。本研究旨在评估 2015 年巴西东南部发生的世界最大采矿灾难后富铁尾矿中的地球化学变化,并预测对河口的潜在环境影响。在三个不同时间(2015 年、2017 年和 2019 年)研究了尾矿的矿物学特征,以评估活跃的氧化还原环境如何影响 Fe 氢氧化物,并估计发生重大变化的时间范围。研究结果表明,Fe 氢氧化物的结晶度大幅下降,最初由高度结晶的 Fe 氢氧化物(即针铁矿和赤铁矿)组成,占 93%,而结晶度较差的 Fe 氢氧化物(即纤铁矿和水铁矿)占 6.7%。在 4 年内,Fe 氢氧化物的矿物学特征发生了转变,2019 年,结晶度较差的 Fe 氢氧化物占 Fe 形态的 47%。扫描电子显微镜的微观照片和平均晶体尺寸证明,针铁矿在 d 方向上的粒径从 109nm 减小到 49nm。平均晶体尺寸的变化增加了 Fe 氢氧化物的反应性,导致与阳离子和阴离子物种的相互作用增加。结晶度的降低和反应性的增加使化合物更容易受到还原溶解的影响。总的来说,研究结果表明,Fe 氢氧化物的结晶度降低以及对还原溶解的更高敏感性会影响环境有害元素(例如磷和痕量金属)的命运,从而增加河口土壤和水中这些污染物的浓度。

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