The reactivity of iron oxides towards reductive dissolution with ascorbic acid in a shallow sandy aquifer - (Romo, Denmark)

The pool of iron oxides, available in sediments for reductive dissolution, is usually estimated by wet chemical extraction methods. Such methods are basically empirically defined and calibrated against various synthetic iron oxides. However, in natural sediments, iron oxides are present as part of a complex mixture of iron oxides with variable crystallinity, clays and organics etc. Such a mixture is more accurately described by a reactive continuum covering a range from highly reactive iron oxides to non-reactive iron oxide. The reactivity of the pool of iron oxides in sediment can be determined by reductive dissolution in 10 mM ascorbic acid at pH 3. Parallel dissolution experiments in HCl at pH 3 reveal the release of Fe(II) by proton assisted dissolution. The difference in Fe(II)-release between the two experiments is attributed to reductive dissolution of iron oxides and can be quantified using the rate equation J/m(0) = k'(m/m(0))(gamma), where J is the overall rate of dissolution (mol s(-1)), m(0) the initial amount of iron oxide, k' a rate constant (s(-1)), m/m(0) the proportion of undissolved mineral and gamma a parameter describing the change in reaction rate over time. In the Romo aquifer, Denmark, the reduction of iron oxides is an important electron accepting process for organic matter degradation and is reflected by the steep increase in aqueous Fe2+ over depth. Sediment from the Romo aquifer was used for reductive dissolution experiments with ascorbic acid. The rate parameters describing the reactivity of iron oxides in the sediment are in the range k' = 7 center dot 10(-6) to 1 center dot 10(3) s(-1) and y = 1 to 2.4. These values are intermediate between a synthetic 2-line ferrihydrite and a goethite. The rate constant increases by two orders of magnitude over depth suggesting an increase in iron oxide reactivity with depth. This increase was not captured by traditional oxalate and dithionite extractions. (c) 2006 Elsevier Inc. All rights reserved.