Enhanced oxidative activity of zero-valent iron by citric acid complexation

• Published in: Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2019-10, Vol.373, p.891-901
• Main Authors: Xu, Yake, Zeng, Lingyu, Li, Lanqing, Chang, Yoon-Seok, Gong, Jianyu
• Format: Article
• Language: English
• Subjects: Citric acid; Iron citrate complexes; Reactive oxygen species; Zero valent iron
• ISSN: 1385-8947; 1873-3212
• DOI: 10.1016/j.cej.2019.05.093

[Display omitted] •The degradation of 4-CP by Fe0-CA is much higher than that of Fe0.•CA could significantly accelerate the release of Fe2+.•Fe(II)[Cit]− is the key species on the degradation of 4-CP.•The transportation of electron from Fe0 to O2 was accelerated because of CA. In this study, we systematically investigated the oxidative degradation of 4-chlorophenol (4-CP) using nano zero valent iron (nZVI, Fe0) cooperated with citric acid (CA), and the role of CA as well as the mechanism of oxidation were deeply evaluated. 56.2% of 4-CP was removed after 60 min under dark condition without any ventilation of oxygen in the presence of Fe0 and CA. The addition of CA accelerated the release of ferrous ions and promoted the Fenton reaction to generate much more reactive oxygen species (ROS), which was confirmed by EPR. The MINEQL+ 4.6 soft was utilized to calculated the existent species in Fe0-CA system, and Fe(II)[Cit]− was found to be the key species playing an important role on the degradation of 4-CP. Fe(II)[Cit]− adsorbed on iron surface accelerated the transportation of electron from Fe0 to O2 to produce more OH. This study puts forward the possible mechanism of generating ROS on Fe0 enhanced by CA and provides an application for the oxidation of pollutants.