不同C/Fe摩尔比铁-黄腐酸配合物对Cr(VI)的吸附-还原行为

Yangyang Zhang, Yuxin Chen, Junwen An, Xiaofei Zhao, Bo Zu
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摘要

水合铁和黄腐酸是土壤中常见的成分,对土壤中Cr(VI)的环境行为有显著影响。先前的研究分别研究了铁酸盐和黄腐酸对Cr(VI)的吸附行为;然而,在土壤中普遍存在的铁-黄腐酸络合物对Cr(VI)的吸附还原能力研究较少。本研究合成了不同C/Fe摩尔比的富里酸-铁酸配合物(Fh-FA),并采用间歇实验、FTIR、BET、XRD、SEM-EDS和XPS等手段研究了Cr(VI)在Fh-FA上的吸附还原行为。结果表明,拟二级动力学模型能较好地描述Fh-FA在Cr(VI)上的吸附过程,该吸附过程可分为快速吸附(0 ~ 30 min)、慢吸附(30 ~ 120 min)和反应平衡(>120 min)三个阶段。Cr(VI)在Fh-FA上的吸附主要通过化学吸附进行。FTIR和XPS分析表明,Cr(VI)最初被Fe-OH吸附在Fh-FA表面。然而,随着Fh-FA的C/Fe摩尔比的增加,更多的Fe- oh被FA中的-COOH络合,导致Fh-FA对Cr(VI)的吸附能力下降。随着C/Fe摩尔比的增加,FA中酚羟基的数量也增加,为Cr(VI)还原为Cr(III)提供了额外的电子。本研究不仅强调了铁-黄腐酸配合物对Cr(VI)的吸附-还原行为,还揭示了C/Fe摩尔比与Cr(VI)吸附-还原之间的相互作用,有助于更全面地了解土壤环境中铁氢氧化物与天然有机质的相对作用。这些发现对土壤中Cr(VI)的管理,提高我们保护和维持环境质量的能力具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Adsorption-Reduction Behavior of Cr(VI) by Ferrihydrite-Fulvic Acid Complexes with Different C/Fe Mole Ratios
Ferrihydrite and fulvic acid are prevalent components of soils and can significantly influence the environmental behavior of Cr(VI) in these matrices. Prior research has investigated the sorption behavior of Cr(VI) by ferrihydrite and fulvic acid independently; however, the sorption-reduction capacity of Cr(VI) by the ferrihydrite-fulvic acid complex, which is ubiquitously present in soils, has been less explored. In this study, ferrihydrite-fulvic acid complexes (Fh-FA) with varying C/Fe mole ratios were synthesized, and the adsorption-reduction behaviors of Cr(VI) on Fh-FA were examined using batch experiments, FTIR, BET, XRD, SEM-EDS, and XPS. The results demonstrate that the pseudo-second-order kinetic model can accurately describe the adsorption process of Fh-FA on Cr(VI), which can be delineated into three stages: rapid adsorption (0-30 min), slow adsorption (30-120 min), and reaction equilibrium (>120 min). The adsorption of Cr(VI) on Fh-FA primarily occurs through chemisorption. FTIR and XPS analyses revealed that Cr(VI) is initially adsorbed by Fe-OH on the Fh-FA surface. However, as the C/Fe mole ratio of Fh-FA increases, more Fe-OH is complexed by -COOH from FA, resulting in a decrease in the adsorption capacity of Cr(VI) by Fh-FA. The number of phenolic hydroxyl groups from FA also increases, providing additional electrons to reduce Cr(VI) to Cr(III) with increasing C/Fe mole ratio. This study not only emphasizes the adsorption-reduction behavior of Cr(VI) by ferrihydrite-fulvic acid complexes but also uncovers the interplay between C/Fe mole ratios and Cr(VI) adsorption-reduction, contributing to a more comprehensive understanding of the relative roles of Fe hydroxides and natural organic matter in soil environments. These findings have significant implications for Cr(VI) management in soils, enhancing our capability to protect and sustain the environmental quality.
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