Photodissolution of Ferrihydrite in the Presence of Oxalic Acid: An In Situ ATR-FTIR/DFT Study

• Published in: Langmuir Vol. 26; no. 21; pp. 16246 - 16253
• Main Authors: Bhandari, Narayan, Hausner, Douglas B, Kubicki, James D, Strongin, Daniel R
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 02.11.2010
• Subjects: Adsorption; Ferric Compounds - chemistry; Interfaces: Adsorption, Reactions, Films, Forces; Oxalic Acid - chemistry; Photochemistry; Quantum Theory; Spectroscopy, Fourier Transform Infrared; Surface Properties; Vibration
• ISSN: 0743-7463; 1520-5827; 1520-5827
• DOI: 10.1021/la101357y

The photodissolution of the iron oxyhydroxide, ferrihydrite, in the presence of oxalic acid was investigated with vibrational spectroscopy, density functional theory (DFT) calculations, and batch geochemical techniques that determined the composition of the solution phase during the dissolution process. Specifically, in situ attenuated total reflection Fourier transform infrared spectroscopy (ATR- FTIR) was used to determine the structure of the adsorbed layer during the dissolution process at a solution pH of 4.5. DFT based computations were used to interpret the vibrational data associated with the surface monolayer in order to help determine the structure of the adsorbed complexes. Results showed that at pH 4.5, oxalate adsorbed on ferrihydrite adopted a mononuclear bidentate (MNBD) binding geometry. Photodissolution at pH 4.5 exhibited an induction period where the rate of Fe(II) release was limited by a low concentration of adsorbed oxalate due to the site-blocking of carbonate that was intrinsic to the surface of the ferrihydrite starting material. Oxalate displaced this initial carbonate over time, and the dissolution rate showed a corresponding increase. Irradiation of oxalate/ferrihydrite at pH 4.5 also ultimately led to the appearance of carbonate reaction product (distinct from carbonate intrinsic to the starting material) on the surface.