Encyclopedia

  • Enhanced oxidative activity of zero-valent iron by citric acid complexation
  • Add time:07/16/2019         Source:sciencedirect.com

    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.

    We also recommend Trading Suppliers and Manufacturers of [R-(R*,R*)]-tartaric acid, iron potassium salt (cas 14948-71-1). Pls Click Website Link as below: cas 14948-71-1 suppliers


    Prev:Fluorescence intensity ratio and lifetime thermometry of praseodymium phosphates for temperature sensing
    Next: Corrosion resistance of 2524 Al alloy anodized in tartaric-sulphuric acid at different voltages and protected with a TEOS-GPTMS hybrid sol-gel coating)

About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia

Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog

©2008 LookChem.com,License: ICP

NO.:Zhejiang16009103

complaints:service@lookchem.com Desktop View