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Reduction of Substituted Nitrobenzenes by Fe(Ⅱ) in Aqueous Mineral Suspensions

机译:Fe(Ⅱ)在矿物质悬浮液中还原取代的硝基苯

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The kinetics of the reduction of 10 monosubstituted nitrobenzenes (NBs) by Fe(Ⅱ) has been investigated under various experimental conditions in aqueous suspensions of minerals commonly present in soils and sediments. Aqueous solutions of Fe(Ⅱ) were unreactive. In suspensions of Fe(Ⅲ)-containing minerals (magnetite, goethite, and lepidocrocite), Fe(Ⅱ) readily reduced the NBs to the corresponding anilines in a strongly pH-dependent reaction. Our results suggest that on other mineral surfaces (γ-aluminum oxide, amorphous silica, titanium dioxide, and kaolinite) iron (hydr)oxide coatings are indispensable to promote the reduction of NBs by adsorbed Fe(Ⅱ). Apparent pseudo-first-order rate constants, k_(obs), were used to describe the initial kinetics of the NB reduction, covering several half-lives of the compounds. The distinct effect of substituents on k_(obs) and the observed pronounced competition between different NBs indicate that precursor complex formation as well as the (re)generation of reactive surface sites are rate-determining steps in the overall reduction of the NBs. The results of this study demonstrate that Fe(Ⅱ) adsorbed on iron (hydr)oxide surfaces or surface coatings may play an important role in the reductive transformation of organic pollutants in subsurface environments. Our findings may also contribute to a better understanding of the various redox processes involved in groundwater remediation techniques based on Fe(0) as the bulk reductant.
机译:在各种实验条件下,研究了土壤和沉积物中通常存在的矿物质的水悬浮液中Fe(Ⅱ)还原10个单取代硝基苯(NBs)的动力学。 Fe(Ⅱ)的水溶液不反应。在含Fe(Ⅲ)的矿物(磁铁矿,针铁矿和纤铁矿)的悬浮液中,Fe(Ⅱ)在很强的pH依赖性反应中很容易将NBs还原为相应的苯胺。我们的结果表明,在其他矿物表面(γ-氧化铝,无定形二氧化硅,二氧化钛和高岭石)上,氧化铁(氢)涂层对于促进吸附的Fe(Ⅱ)还原NBs必不可少。使用表观的伪一级速率常数k_(obs)来描述NB还原的初始动力学,涵盖化合物的数个半衰期。取代基对k_(obs)的不同影响以及不同NB之间观察到的明显竞争表明,前体复合物的形成以及反应性表面位点的(再生)是整个NB还原过程中的决定速率的步骤。这项研究的结果表明,吸附在氧化铁表面或表面涂层上的Fe(Ⅱ)可能在地下环境中有机污染物的还原转化中起重要作用。我们的发现也可能有助于更好地理解基于Fe(0)作为主要还原剂的地下水修复技术中涉及的各种氧化还原过程。

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