Bridging arsenate surface complexes on the hematite ( 012 ) surface q

The fate of the oxoanion arsenate in diverse systems is strongly affected by its adsorption on the surfaces of iron (oxyhydr)oxide minerals. Predicting this behavior in the environment requires an understanding of the mechanisms of arsenate adsorption. In this study, the binding site and adsorption geometry of arsenate on the hematite (012) surface is investigated. The structure and termination of the hematite (012)-water interface were determined by high resolution X-ray reflectivity, revealing that two distinct terminations exist in a roughly 3:1 proportion. The occurrence of multiple terminations appears to be a result of sample preparation, and is not intrinsic to the hematite (012) surface. X-ray standing wave (XSW) measurements were used to determine the registry of adsorbed arsenate to the hematite structure, and thus the binding site and geometry of the resulting surface complex. Arsenate forms a bridging bidentate complex on two adjacent singly coordinated oxygen groups on each of the two distinct terminations present at the hematite surface. Although this geometry is consistent with that seen in past studies, the derived As–Fe distances are longer, the result of the topology of the FeO6 octahedra on the (012) surface. As EXAFS-derived As–Fe distances are often used to determine the adsorption mechanism in environmental samples (e.g., mine tailings, contaminated sediments), this demonstrates the importance of considering the possible sorbent surface structures and arrangements of adsorbates when interpreting such data. As multiple functional groups are present and multiple binding geometries are possible on the hematite (012) surface, the XSW data suggest that formation of bridging bidentate surface complexes on singly coordinated oxygen sites is the preferred adsorption mechanism on this and most other hematite surfaces (provided those surfaces contain adjacent singly coordinated oxygen groups). These measurements also constrain the likely reaction stoichiometry, with only the protonation state of the surface complex undetermined. Although bridging bidentate inner-sphere surface complexes comprised the majority of the adsorbed arsenate present on the hematite (012) surface, there is an additional population of sorbed arsenate species that could not be characterized by the XSWmeasurements. These species are likely more disordered, and thus more weakly bound, than the bridging bidentate complexes, and may play a role in determining the fate, transport, and bioavailability of arsenate in the environment. Finally, the possibility of obtaining species-specific XSW measurements by tuning the incident beam energy to specific features in a XANES spectrum is described. 2007 Published by Elsevier Ltd. 0016-7037/$ see front matter 2007 Published by Elsevier Ltd. doi:10.1016/j.gca.2007.01.015 q The submitted manuscript has been created by UChicago Argonne, LLC, Operator of Argonne National Laboratory (‘‘Argonne’’). Argonne, a U.S. Department of Energy Office of Science laboratory, is operated under Contract No. DE-AC02-06CH11357. The U.S. Government retains for itself, and others acting on its behalf, a paid-up nonexclusive, irrevocable worldwide license in said article to reproduce, prepare derivative works, distribute copies to the public, and perform publicly and display publicly, by or on behalf of the Government. * Corresponding author. Fax: +1 630 252 9570. E-mail address: [email protected] (J.G. Catalano). 1884 J.G. Catalano et al. / Geochimica et Cosmochimica Acta 71 (2007) 1883–1897