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土壤提取液中 pH 值对铁形态的影响:天然有机物与铁矿物纳米粒子的配合物。

The influence of pH on iron speciation in podzol extracts: iron complexes with natural organic matter, and iron mineral nanoparticles.

机构信息

University of Vienna, Department of Environmental Geosciences, Althanstraße 14, 1090 Vienna, Austria.

出版信息

Sci Total Environ. 2013 Sep 1;461-462:108-16. doi: 10.1016/j.scitotenv.2013.04.076. Epub 2013 May 25.

DOI:10.1016/j.scitotenv.2013.04.076
PMID:23712121
Abstract

The quantities of natural organic matter (NOM) and associated iron (Fe) in soil extracts are known to increase with increasing extractant pH. However, it was unclear how the extraction pH affects Fe speciation for particles below 30 nm. We used flow field-flow fractionation (FlowFFF) and transmission electron microscopy (TEM) to investigate the association of Fe and trace elements with NOM and nanoparticulate iron (oxy)hydroxides in podzol extracts. For extracts prepared at the native soil pH (4), and within a 1-30 nm size range, Fe was associated with NOM. In extracts with a pH≥7 from the E and B soil horizons, Fe was associated with NOM as well as with iron (oxy)hydroxide nanoparticles with a size of approximately 10 nm. The iron (oxy)hydroxide nanoparticles may have either formed within the soil extracts in response to the increase in pH, or they were mobilized from the soil. Additionally, pH shift experiments showed that iron (oxy)hydroxides formed when the native soil pH (4) was increased to 9 following the extraction. The iron (oxy)hydroxide nanoparticles aggregated if the pH was decreased from 9 to 4. The speciation of Fe also influenced trace element speciation: lead was partly associated with the iron (oxy)hydroxides (when present), while copper binding to NOM remained unaffected by the presence of iron (oxy)hydroxide nanoparticles. The results of this study are important for interpreting the representativeness of soil extracts prepared at a pH other than the native soil pH, and for understanding the changes in Fe speciation that occur along a pH gradient.

摘要

土壤浸提液中天然有机物(NOM)和相关铁(Fe)的含量已知随浸提剂 pH 值的增加而增加。然而,提取 pH 值如何影响粒径小于 30nm 的颗粒中 Fe 的形态仍不清楚。我们使用流场分离(FlowFFF)和透射电子显微镜(TEM)研究了在灰壤浸提液中,NOM 与痕量元素以及纳米级铁(氢)氧化物之间的结合情况。对于在原生土壤 pH 值(约 4)下制备的提取物,以及在 1-30nm 的粒径范围内,Fe 与 NOM 结合。在 E 和 B 土壤层的 pH 值≥7 的提取物中,Fe 与 NOM 以及粒径约为 10nm 的铁(氢)氧化物纳米颗粒结合。这些铁(氢)氧化物纳米颗粒可能是在 pH 值升高的情况下在土壤浸提液中形成的,也可能是从土壤中迁移出来的。此外,pH 值变化实验表明,在提取后将原生土壤 pH 值(约 4)升高至 9 时会形成铁(氢)氧化物。如果将 pH 值从 9 降低至 4,铁(氢)氧化物纳米颗粒会聚集。Fe 的形态也会影响痕量元素的形态:当存在铁(氢)氧化物时,部分铅与铁(氢)氧化物结合,而铜与 NOM 的结合不受铁(氢)氧化物纳米颗粒的影响。本研究的结果对于解释在原生土壤 pH 值以外的 pH 值下制备的土壤浸提液的代表性以及理解 pH 梯度下 Fe 形态的变化非常重要。

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