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从铁(III)离子到水铁矿,再到赤铁矿。

From Fe(III) Ions to Ferrihydrite and then to Hematite.

作者信息

Schwertmann U, Friedl J, Stanjek H

机构信息

Institute for Soil Science, Technical University, Freising, Munich, D 85350, Germany

出版信息

J Colloid Interface Sci. 1999 Jan 1;209(1):215-223. doi: 10.1006/jcis.1998.5899.

Abstract

The pathways from soluble Fe(III)-aquo ions to various solid polymeric Fe(III) oxides of increasing thermodynamic stability involve intermediate products which are still only partly known. This paper combines results from the literature with own new results from X-ray diffraction, Mössbauer spectroscopy, and electron microscopy. It is maintained that no intermediate phases were positively identified between mono-, di-, and trimers and a range of solid polynuclear phases. This indicates fast polymerisation as the OH/Fe ratio of the system increases. The immediate solid polynuclear phases are poorly crystalline Fe(III)-oxyhydroxy salts and a range of oxyhydroxides, called ferrihydrites in mineralogy, with varying crystallinity and magnetic ordering behavior. The rate of hydrolysis as affected by pH, rate of OH addition and temperature is of paramount importance for the nature of these polymeric phases. In the presence of free or surface-bound water, the transformation of ferrihydrite into the stable end product hematite (alpha-Fe2O3) proceeds by crystallization within the ferrihydrite aggregate and is enhanced as the pH approaches the zero point of charge as well as by Al in the system. This mechanism is different from that in nonaqueous systems. Copyright 1999 Academic Press.

摘要

从可溶性水合铁(III)离子到热力学稳定性不断增加的各种固态聚合铁(III)氧化物的途径涉及一些中间产物,而这些中间产物目前仍仅部分为人所知。本文将文献结果与来自X射线衍射、穆斯堡尔光谱和电子显微镜的新结果相结合。研究认为,在单体、二聚体和三聚体与一系列固态多核相之间未明确鉴定出中间相。这表明随着体系中OH/Fe比值的增加,聚合反应迅速发生。直接形成的固态多核相是结晶性较差的铁(III)羟基氧盐和一系列氢氧化物,在矿物学中称为水铁矿,它们具有不同的结晶度和磁有序行为。受pH值、OH添加速率和温度影响的水解速率对于这些聚合相的性质至关重要。在存在游离或表面结合水的情况下,水铁矿向稳定终产物赤铁矿(α-Fe2O3)的转变通过在水铁矿聚集体内结晶进行,并且随着pH值接近零电荷点以及体系中Al的存在而增强。这种机制与非水体系中的不同。版权所有1999年学术出版社。

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