Role of Dissolved Organic Matter in the Release of Chromium from Schwertmannite: Kinetics, Repartition, and Mechanisms.

Abstract

Dissolved organic matter (DOM) is an important factor influencing mineral biogeochemistry, although the role of labile DOM in the release of chromium (Cr) from schwertmannite, a mineral with high surface area, is unclear. In this study, the interaction of DOM with synthetic CrO-schwertmannite was investigated to better understand the potential fate of Cr in high-DOM environments. Minerals and their products were analyzed using Fourier transform infrared spectroscopy, X-ray diffraction, transmission electron microscopy, scanning electron microscopy, and X-ray photoelectron spectroscopy. Experiments were conducted at pH 3.2 or 6.5 for different lengths of time, with a shrinking core model developed to describe kinetic processes. The concentration of total Cr in solution reached a maximum when the pH was 6.5 and the concentration of L-tryptophan was 5 mM. The newly formed minerals were confirmed to be mixtures involving residual schwertmannite, goethite, ferrihydrite, and jarosite. A possible mechanism is proposed to be a ligand-controlled binary system, accompanied by possible reduction at acidic pH conditions (3.2), including mass transfer and charge transfer processes. This study gives a new perspective for understanding the reactivity and stability of schwertmannite in the environment; it also provides some predictions on the mobility and fate of Cr. These findings will help design remediation strategies for Cr contamination.