Structural evolution of Cr(III) polymeric species at the gamma-Al2O3/waterinterface

We have characterized the structure of the predominant Cr(III) species pres ent at the gamma -Al2O3/water interface as a function of equilibration time and Cr(III) surface loading using X-ray absorption fine structure (XAFS) s pectroscopy. The spectroscopic measurements span two distinct time periods of Cr(III) uptake. During the initial period (<2 h), which is characterized by rapid uptake, Cr(III) monomers form inner-sphere complexes on the <gamm a>-Al2O3 surface by bonding to at least two surface functional groups. Duri ng the second period (ranging from 2 h to 1 week), significant quantities o f Cr(III) continue to be removed from solution, but sorption proceeds at a greatly reduced rate. The XAFS spectra collected during the period of slow uptake show an increase in scattering contributions from neighboring Cr(III ) atoms with increasing equilibration time. The inferred structural changes are consistent with a progression from hydroxo-bridged Cr(III) dimers to h igher-order polymers. In combination with spectroscopic evidence, which sho ws that monomeric Cr(III) species are the only significant reactants in sol ution, the observed evolution of Cr(III) surface species suggests that chem ical bonding between adsorbed Cr(III) ions and gamma -Al2O3 surface functio nal groups enhances Cr(III) polymerization. The proposed reaction sequence has important implications for surface complexation modeling used to predic t Cr(III) partitioning by hydroxide sorbents in wastewater treatment and co ntaminant migration scenarios.