Abstract
The kinetics of Cr(VI) reduction to Cr(III) by carbonate green rust were studied for a range of reactant concentrations and pH values. Carbonate green rust, [FeII4FeIII2(OH)12][4H2O x CO3], was synthesized by induced hydrolysis (i.e., coprecipitation) of an Fe(ll)/Fe(III) solution held at a constant pH of 8. An average specific surface area of 47 +/- 7 m2 g(-1) was measured for five separate batches of freeze-dried green rust precipitate. Heterogeneous reduction by Fe(II) associated with the carbonate green rust appears to be the dominant pathway controlling Cr(VI) loss from solution. The apparent stoichiometry of the reaction between ferrous iron associated with green rust ([Fe(II)GR]) and Cr(VI) was slightly higherthan the expected 3:1 ratio, possibly due to the presence of other oxidants, such as oxygen, protons, or interlayer carbonate ions. The rate of Cr(VI) reduction was proportional to the green rust surface area concentration, and psuedo-first-order rate coefficients (kobs) ranging from 1.2 x 10(-3) to 11.2 x 10(-3) s(-1) were determined. The effect of pH was small with a 5-fold decrease in rate with increasing pH (from 5.0 to 9.0). At low Cr(VI) concentrations (<200 microM), the rate of reaction was first order with respect to Cr(VI) concentration, whereas, at high Cr(VI) concentrations, rates appearto deviate from first-order kinetics and approach a constant value. Estimated amounts of surface Fe(II) and total Fe(II) suggest that the deviation from first-order kinetics observed at higher Cr(VI) concentrations and the 50-fold decrease in rate observed upon three sequential exposures to Cr(VI) is due to exhaustion of available Fe(II).
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.