NOTE: This material may be protected by copyright law (Title 17, U.S. Code).

Peak, D., R.G. Ford, and D.L. Sparks. 1999. An in-situ ATR-FTIR investigation of sulfate bonding mechanisms on goethite. J. Colloid Interf. Sci. 218:289-299.



The mechanism of sulfate adsorption on goethite was investigated in situ using attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. Sulfate adsorption was investigated at ionic strengths between 0.005 and 0.1 M, reactant concentrations between 5 and 500 M, and pH values between 3.5 and 9.0. It was determined that sulfate forms both outer-sphere and inner-sphere surface complexes on goethite at pH less than 6. At pH values greater than 6, sulfate adsorbs on goethite only as an outer-sphere complex. The relative amount of outer-sphere sulfate surface complexation increased with decreasing ionic strength. The spectrum of sulfate adsorbed on goethite was also compared to the infrared spectrum of synthetic schwertmannite, an iron(III) oxy-hydroxy-sulfate. It was determined that in situ spectra of both schwertmannite and adsorbed sulfate are quite similar, suggesting that a continuum of outer- and inner-sphere sulfate occurs in both cases. Copyright 1999 Academic Press.

Key Words:  sulfate; surface complexation; ATR-FTIR; goethite; bonding mechanisms; in situ spectroscopy; schwertmannite

Home | Members | News | Links | Research | Photos | Awards | Alumni | Publications