4.7 Article

Degradation of azo dye Orange G in aqueous solutions by persulfate with ferrous ion

Journal

SEPARATION AND PURIFICATION TECHNOLOGY
Volume 72, Issue 1, Pages 105-111

Publisher

ELSEVIER
DOI: 10.1016/j.seppur.2010.01.012

Keywords

Orange G; Degradation; Kinetics; Persulfate; Fe2+

Funding

  1. Hong Kong Polytechnic University
  2. [G-YX0 M]

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The oxidative degradation of azo dye, Orange G (OG), in aqueous solutions by the persulfate/Fe2+ reagent has been investigated. Effects of pH, dosages of persulfate and Fe2+, temperature, and the presence of inorganic ions (Cl-, NO3-, HCO3- and H2PO4-) on OG degradation were examined in batch experiments. The OG degradation by the persulfate/Fe2+ reagent was found to follow the first-order kinetic model. Under an optimum condition ([persulfate] = 4 mM, [Fe2+] = 4 mM and pH 3.5), the OG degradation in aqueous solutions with an initial concentration of 0.1 mM was achieved by 99% within 30 min. The OG degradation increased with an increased dosage of both persulfate and Fe2+. The experimental results showed that increasing the reaction temperature from 293 to 313 K was beneficial to the OG degradation, but not as efficient as chemical activation with Fe2+ at ambient temperature. In the meantime, the apparent activation energy for the OG degradation was determined to be 92.2 kJ mol(-1). Furthermore, the results demonstrated that the OG degradation could be significantly inhibited due to the existence of inorganic ions in a sequence of NO3- < HCO3-. The experiments also demonstrated that the persulfate/Fe2+ reagent can degrade OG in aqueous solutions to a higher degree than the Fenton's reagent, which is beneficial to the mineralization of azo dyes. (C) 2010 Elsevier B.V. All rights reserved.

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