| Literature DB >> 11254288 |
John D. Ostergren1, Gordon E. Brown, George A. Parks, Per Persson.
Abstract
The effects of sulfate anions on the uptake of Pb(II) onto goethite were investigated at the molecular level using in situ Pb L(III)-EXAFS and ATR-FTIR spectroscopies. Macroscopic uptake data show that Pb uptake can be enhanced by at least 30% at pH 5 in the presence of 3.16 mM sulfate and that sulfate uptake at pH 7 can be enhanced by more than a factor of 3 in the presence of 1.0 mM Pb. Consistent with behavior in sulfate-free systems, Pb(II) forms inner-sphere complexes sharing either corners or edges with Fe(O,OH)(6) octahedra under all conditions studied. The relative fraction of corner-sharing complexes is, however, significantly enhanced in the presence of sulfate at pH 5, 6, and 7 (all conditions studied) and additional sulfate species with C(3v) or lower point symmetry were noted in the presence of Pb by ATR-FTIR. Drawing on bond valence and structural constraints developed in J. D. Ostergren et al. (2000, J. Colloid Interface Science 224, 000-000), these results indicate formation of Type A ternary complexes bonded to the surface through Pb that is bound as a bridging bidenate complex to two adjacent A-type (singly coordinated) surface oxygens (( identical withFe-O)(2)-Pb-OSO(3)). Copyright 2000 Academic Press.Entities:
Year: 2000 PMID: 11254288 DOI: 10.1006/jcis.1999.6702
Source DB: PubMed Journal: J Colloid Interface Sci ISSN: 0021-9797 Impact factor: 8.128