4.6 Article

Degradation of p-chloroaniline by FeO3-xH3-2x/Fe0 in the presence of persulfate in aqueous solution

Journal

RSC ADVANCES
Volume 5, Issue 51, Pages 41079-41087

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5ra02221e

Keywords

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Funding

  1. Fundamental Research Funds of Guangdong Provincial Key Laboratory of Atmospheric environment and Pollution Control (China) [2011A060901011]
  2. Fundamental Research Funds of State Key Lab of Subtropical Building Science, South China University of Technology [2015ZB25]
  3. China Postdoctoral Science Foundation Funded Project [2014M562185]
  4. Fundamental Research Funds of State Key Laboratory of Pulp and Paper Engineering (China) [201477]

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Sulfate radical based advanced oxidation processes are promising techniques for the removal of organic compounds in aqueous solutions. In this study, FeO3-xH3-2x/Fe-0 catalyst was prepared and used to activate persulfate (S2O82-) for the degradation of p-chloroaniline (PCA). The results showed that nearly complete degradation of PCA was observed within 1 h in the persulfate-FeO3-xH3-2x/Fe-0 system under the following optimized reaction conditions: PCA concentration 0.05 mM, FeO3-xH3-2x/Fe-0 1 g L-1, persulfate 2.5 mM and pH 7.0. The PCA degradation was higher under acidic conditions when compared to alkaline conditions. A complete removal of the added PCA (0.05 mM) was achieved within 5 min with the addition of 2.5 mM persulfate and 1 g L-1 FeO3-xH3-2x/Fe-0 at pH 3.0. FeO3-xH3-2x/Fe-0 catalyst was prepared by the calcination of Fe-0 at 200 degrees C. The morphology of the catalyst was investigated with X-ray diffraction patterns (XRD), Scanning electron microscopy (SEM) and Fourier transform infrared spectra (FTIR). The results demonstrated that the catalyst surface was mainly composed of hematite gamma-Fe2O3 and goethite (alpha-FeOOH).

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