<p>In this work, CoFe-layered double metal oxide (CoFe-LDO) was obtained by a co-precipitation-calcination route using CoFe-layered double metal hydroxide (CoFe-LDH) as precursor material, and then MoS<sub>2</sub> and chitosan-derived N-doped carbon co- modified CoFe-LDO composite catalyst (MoS<sub>2</sub>@CoFe-LDO/NCS) was prepared. This material was characterized by SEM, EDS, FTIR, XRD and XPS, and was synthesized to catalyze ozonation for the degradation of methylene blue (MB). The influence of CoFe-LDO dosage, O<sub>3</sub> flow rate, initial MB concentration, catalyst dosage, initial pH and coexisting compounds on MB&#xa0;removal efficiency were systematically investigated. The decomposition efficiency of 50&#xa0;mg/L MB by 10%MoS<sub>2</sub>@CoFe-LDO/NCS reached 96.47% within 8&#xa0;min under the conditions of 10% CoFe-LDO dosage (CoFe -LDO:CS), pH = 6.8, catalyst dosage of 0.4 g/L, Ozone flow rate of 1.87 mg/(L⋅min) and 25&#xa0;°C. Stability tests and metal ion leaching experiments confirmed the excellent chemical stability and environmental compatibility of 10%MoS<sub>2</sub>@CoFe-LDO/NCS. Electrochemical characterization showed that 10%MoS<sub>2</sub>@CoFe-LDO/NCS possessed enhanced current density, redox activity and excellent electron transfer capability. Quenching experiments revealed that <sup>1</sup>O<sub>2</sub>, O<sub>2</sub><sup><b>∙</b>−</sup> and <b>∙</b>OH contributed to the MB degradation process, with O<sub>2</sub><sup><b>∙</b>−</sup> confirmed as the dominant reactive species.</p>

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Catalytic Ozone Decomposition of Methylene Blue by MoS2 and Chitosan-Derived N-Doped Carbon Co-Modified CoFe-LDO

  • Yuanfang Yang,
  • Yunlan Xu,
  • Danli Tang,
  • Tanxia Xiang

摘要

In this work, CoFe-layered double metal oxide (CoFe-LDO) was obtained by a co-precipitation-calcination route using CoFe-layered double metal hydroxide (CoFe-LDH) as precursor material, and then MoS2 and chitosan-derived N-doped carbon co- modified CoFe-LDO composite catalyst (MoS2@CoFe-LDO/NCS) was prepared. This material was characterized by SEM, EDS, FTIR, XRD and XPS, and was synthesized to catalyze ozonation for the degradation of methylene blue (MB). The influence of CoFe-LDO dosage, O3 flow rate, initial MB concentration, catalyst dosage, initial pH and coexisting compounds on MB removal efficiency were systematically investigated. The decomposition efficiency of 50 mg/L MB by 10%MoS2@CoFe-LDO/NCS reached 96.47% within 8 min under the conditions of 10% CoFe-LDO dosage (CoFe -LDO:CS), pH = 6.8, catalyst dosage of 0.4 g/L, Ozone flow rate of 1.87 mg/(L⋅min) and 25 °C. Stability tests and metal ion leaching experiments confirmed the excellent chemical stability and environmental compatibility of 10%MoS2@CoFe-LDO/NCS. Electrochemical characterization showed that 10%MoS2@CoFe-LDO/NCS possessed enhanced current density, redox activity and excellent electron transfer capability. Quenching experiments revealed that 1O2, O2 and OH contributed to the MB degradation process, with O2 confirmed as the dominant reactive species.