White Rose University Consortium logo
University of Leeds logo University of Sheffield logo York University logo

A revised scheme for the reactivity of iron (oxyhydr)oxide minerals towards dissolved sulfide

Poulton, S.W., Krom, M.D. and Raiswell, R. (2004) A revised scheme for the reactivity of iron (oxyhydr)oxide minerals towards dissolved sulfide. Geochimica et Cosmochimica Acta, 68 (18). pp. 3703-3715. ISSN 0016-7037

Full text available as:
[img]
Preview
Text
raiswellr7.pdf
Available under licence : See the attached licence file.

Download (413Kb)

Abstract

The reaction between dissolved sulfide and synthetic iron (oxyhydr)oxide minerals was studied in artificial seawater and 0.1 M NaCl at pH 7.5 and 25°C. Electron transfer between surface-complexed sulfide and solid phase Fe(III) results in the oxidation of dissolved sulfide to elemental sulfur, and the subsequent dissolution of the surface-reduced Fe. Sulfide oxidation and Fe(II) dissolution kinetics were evaluated for freshly precipitated hydrous ferric oxide (HFO), lepidocrocite, goethite, magnetite, hematite, and Al-substituted lepidocrocite. Reaction kinetics were expressed in terms of an empirical rate equation of the form:

R-i = k(i)(H2S)(t=0)(0.5)A

where Ri is the rate of Fe(II) dissolution (RFe) or the rate of sulfide oxidation (RS), ki is the appropriate rate constant (kFe or kS), (H2S)t=0 is the initial dissolved sulfide concentration, and A is the initial mineral surface area. The rate constants derived from the above equation suggest that the reactivity of Fe (oxyhydr)oxide minerals varies over two orders of magnitude, with increasing reactivity in the order, goethite < hematite < magnetite << lepidocrocite ≈ HFO. Competitive adsorption of major seawater solutes has little effect on reaction kinetics for the most reactive minerals, but results in rates which are reduced by 65-80% for goethite, magnetite, and hematite. This decrease in reaction rates likely arises from the blocking of surface sites for sulfide complexation by the adsorption of seawater solutes during the later, slower stages of adsorption (possibly attributable to diffusion into micropores or aggregates). The derivation of half lives for the sulfide-promoted reductive dissolution of Fe (oxyhydr)oxides in seawater, suggests that mineral reactivity can broadly be considered in terms of two mineral groups. Minerals with a lower degree of crystal order (hydrous ferric oxides and lepidocrocite) are reactive on a time-scale of minutes to hours. The more ordered minerals (goethite, magnetite, and hematite) are reactive on a time-scale of tens of days. Substitution of impurities within the mineral structure (as is likely in nature) has an effect on mineral reactivity. However, these effects are unlikely to have a significant impact on the relative reactivities of the two mineral groups.

Item Type: Article
Copyright, Publisher and Additional Information: Copyright © 2004 Elsevier Ltd. This is an author produced version of an article accepted for publication in Geochimica et Cosmochimica Acta.
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Environment (Leeds) > School of Earth and Environment (Leeds)
Depositing User: Repository Officer
Date Deposited: 20 May 2005
Last Modified: 04 Jun 2014 08:34
Published Version: http://www.sciencedirect.com/science/journal/00167...
Status: Published
Refereed: Yes
Identification Number: 10.1016/j.gca.2004.03.012
URI: http://eprints.whiterose.ac.uk/id/eprint/466

Actions (repository staff only: login required)