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Autor(en) / Beteiligte
Titel
Effects of phosphate and silicate on the transformation of hydroxycarbonate green rust to ferric oxyhydroxides
Ist Teil von
  • Geochimica et cosmochimica acta, 2015-12, Vol.171, p.1-14
Ort / Verlag
Elsevier Ltd
Erscheinungsjahr
2015
Link zum Volltext
Quelle
Elsevier ScienceDirect Journals Complete
Beschreibungen/Notizen
  • Hydroxycarbonate green rust (GR1(CO32−)) was prepared by oxidation of aerated aqueous suspensions of Fe(II) hydroxide, and the presence of light promoted the transformation of GR1(CO32−) by dissolved O2 at pH 7.8 and 25°C. Further transformation of GR1(CO32−) in the light was conducted in the presence of orthophosphate (P) or silicate (Si) anions, followed by solution analysis and solid product characterization using X-ray diffraction (XRD), transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy (FTIR). Results show that both P and Si anions significantly affect the transformation of GR1(CO32−) through adsorption on the intermediate products. The time required for complete GR1(CO32−) transformation and the phases, crystallinity and morphology of the transformation products all depend on the Fe/anion molar ratio. When compared to the control, the transformation can be promoted by low Si concentrations but retarded by P. With decreasing Fe/P ratio, the products change from acicular goethite (absence of P) to tabular lepidocrocite (Fe/P: 120-48) and to mixed phases of platelets of ferric GR1(CO32−) (EX-GR1) and minor ferrihydrite (Fe/P: 24-3). In terms of Si, the products are goethites when the Fe/Si ratio of 48-12, and with increasing ratio, the goethite crystallinity and particle size decrease and the morphology changes from acicular (absence of Si) to plate-like or isodimensional particles. The goethite morphology at low Fe/Si ratios is comparable to natural goethite samples commonly found in soils. At Fe/Si=3, the products are EX-GR1 platelets with minor ferrihydrite coexisting. The likely pathway of the oxidative GR1(CO32−) transformation in the control system and in the presence of low concentrations of Si (Fe/Si⩾12) is GR1(CO32−)→amorphous γ-FeOOH-like phase→α-FeOOH via a dissolution–oxidation–precipitation mechanism. In addition, Fe(II) released during dissolution of GR1(CO32−) is adsorbed on the products and the transformation of the γ-FeOOH-like phase to goethite is catalyzed by the adsorbed Fe(II). For the P system, the released Fe(II) forms ternary surface complexes with P on the mineral surfaces without any catalytic role, leading to the formation of lepidocrocite at low P concentrations. Clearly, the oxidative transformation of green rust to various crystalline iron oxyhydroxides depends on the type and concentration (Fe/anion molar ratio) of co-existing anions. This study also suggests that the natural goethite formed by Fe(II) oxidation in the form of plate-like or isodimensional particles is most likely related to the ubiquitous presence of silicates in soil environments.
Sprache
Englisch
Identifikatoren
ISSN: 0016-7037
eISSN: 1872-9533
DOI: 10.1016/j.gca.2015.08.020
Titel-ID: cdi_crossref_primary_10_1016_j_gca_2015_08_020
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