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BULLETIN OF THE CHINESE CERAMIC SOCIETY ›› 2021, Vol. 40 ›› Issue (11): 3762-3768.

• Ceramics • Previous Articles     Next Articles

Catalytic Degradation of Malachite Green by SrFe0.6Co0.4O3

LI Jiafei, XU Kai, ZHANG Yongming, PAN Lisha   

  1. Hainan Provincial Fine Chemical Engineering Research Center, Hainan University, Hainan 570228, China
  • Received:2021-05-18 Revised:2021-06-30 Online:2021-11-15 Published:2021-12-08

Abstract: Malachite green (MG) is a triphenylmethane dye with a complex molecular structure, which is difficult to be degraded, and it makes a difficulty in industrial wastewater treatment. In this paper,based on Goldschmidt radius tolerance rule, the ABO3 type catalysts with formula SrFe(1-x)CoxO3 (x=0~1) for degrading MG was designed. After experimental investigation, the SrFe0.6Co0.4O3 with highest catalytic activity was selected as target catalyst for MG degradation. The characteristics of this catalyst were analysed by XRD, SEM, BET and XPS methods. XRD pattern shows that the catalyst is pure perovskite crystal; the SEM image shows the morphology of catalyst particles is “honeycomb” flake with irregular stacking. In the BET adsorption isotherm of the catalyst, there is no obvious hysteresis loop, which means that there is no pore like “ink bottle”. Seeing from the XPS spectrum of the catalyst, the B-position has four ions (Fe2+/Fe3+ and Co2+/Co3+) at the same time, and the distribution ratio of above four ions vary greatly before and after the catalytic reaction. Based on these results, the mechanism of the catalytic reaction is speculated as follow: at first the Co3+ on B-site with the dissolved oxygen to form active oxygen [O2]+ and Co2+; then the [O2]+ oxidizes the MG, as well as the positive charge of [O2]+ is transferred to the Fe2+ on B-site to form Fe3+; at last, the positive charge of Fe3+ could be transferred to Co2+ on the B-site to form Co3+, and the transfer and circulation of the charge in catalytic process is completed.

Key words: SrFe0.6Co0.4O3 catalyst, malachite green, catalysis, degradation, reaction mechanism, charge transfer

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