Quantification of the Influence of Citrate/Fe(II) Molar Ratio on Hydroxyl Radical Production and Pollutant Degradation during Fe(II)-Catalyzed O2 and H2O2 Oxidation Processes

Abstract

Ligand-enhanced hydroxyl radical (•OH) production is an important strategy for Fe(II)-catalyzed O2 and H2O2 oxidation processes. However, the influence of the molar ratio of ligands to Fe(II) on •OH production remains elusive. This study employed citrate and inorganic dissolved Fe(II) (Fe(II)dis) as the representative ligand and Fe(II) species, respectively, to quantify this relationship. Results showed that •OH production was highly dependent on the citrate/Fe(II) molar ratio. For instance, for the oxygenation of Fe(II)dis, the •OH accumulations were 2.0–8.5, 3.4–28.5 and 8.1–42.3 μM at low (0.25–0.5), moderate (0.5–1), and high (1–2) citrate/Fe(II) molar ratios, respectively. At low citrate/Fe(II) molar ratio (<0.5), inorganic Fe(II)dis mainly contributed to •OH production, with the increase in the citrate/Fe(II) molar ratio to a high level (1–2), Fe(II)-citrate complex turned to the electron source for •OH production. The change in Fe(II) speciation with the increase of citrate/Fe(II) molar ratio elevated •OH production. For pollutant degradation, 1 mg/L phenol was degraded by 53.6% within 40 min during oxygenation of Fe(II)-citrate system (1:1) at pH 7. Our results suggest that a moderate molar ratio of ligand/Fe(II) (0.5–1) may be optimal for Fe(II)-catalyzed O2 and H2O2 oxidation processes.