<p>Macromolecular humic acid (HA) is highly resistant to degradation in wastewater treatment system. Although catalytic wet air oxidation (CWAO) processes can degrade HA, they typically require relatively high temperatures (&gt; 200 °C) to achieve effective degradation. In this study, the effect of hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>) as a radical promoter on the CWAO of HA was investigated using a catalyst of HNO<sub>3</sub>-modified activated carbon (ACNA). Compared with the conventional CWAO process, the addition of H<sub>2</sub>O<sub>2</sub> (44% of the stoichiometric amount needed for complete mineralization of HA) significantly increased the degradation of HA. For example, under moderate conditions of 150 °C and 0.5&#xa0;MPa O<sub>2</sub>, a 4-h treatment with H<sub>2</sub>O<sub>2</sub> achieved a 97.9% reduction in absorbance at 436 nm (Abs<sub>436</sub>) and a 56.9% removal of chemical oxygen demand (COD). In contrast, the conventional system without H<sub>2</sub>O<sub>2</sub> under the same conditions only reached an 82.4% reduction in Abs<sub>436</sub> and a 39.8% removal of COD. In addition, adding H<sub>2</sub>O<sub>2</sub> to the CWAO system (H<sub>2</sub>O<sub>2</sub>-CWAO) significantly enhanced the biodegradability of HA solution. For instance, the BOD<sub>5</sub>/COD ratio increased from 0.19 in the CWAO system to 0.68 in the H<sub>2</sub>O<sub>2</sub>-CWAO system. ACNA showed high stability during HA degradation in the H<sub>2</sub>O<sub>2</sub>-CWAO system, with only minor loss of activity (based on COD removal efficiency) over three cycles. Moreover, the effectiveness of this system was further demonstrated by treating stabilized landfill leachate, increasing the BOD<sub>5</sub>/COD ratio from 0.08 to 0.49.</p>

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Hydrogen Peroxide Promoted Catalytic Wet Air Oxidation of Humic Acid and Landfill Leachate with HNO3-modified Activated Carbon

  • Yanrong Peng,
  • Fen Liu,
  • Shufang Xiong

摘要

Macromolecular humic acid (HA) is highly resistant to degradation in wastewater treatment system. Although catalytic wet air oxidation (CWAO) processes can degrade HA, they typically require relatively high temperatures (> 200 °C) to achieve effective degradation. In this study, the effect of hydrogen peroxide (H2O2) as a radical promoter on the CWAO of HA was investigated using a catalyst of HNO3-modified activated carbon (ACNA). Compared with the conventional CWAO process, the addition of H2O2 (44% of the stoichiometric amount needed for complete mineralization of HA) significantly increased the degradation of HA. For example, under moderate conditions of 150 °C and 0.5 MPa O2, a 4-h treatment with H2O2 achieved a 97.9% reduction in absorbance at 436 nm (Abs436) and a 56.9% removal of chemical oxygen demand (COD). In contrast, the conventional system without H2O2 under the same conditions only reached an 82.4% reduction in Abs436 and a 39.8% removal of COD. In addition, adding H2O2 to the CWAO system (H2O2-CWAO) significantly enhanced the biodegradability of HA solution. For instance, the BOD5/COD ratio increased from 0.19 in the CWAO system to 0.68 in the H2O2-CWAO system. ACNA showed high stability during HA degradation in the H2O2-CWAO system, with only minor loss of activity (based on COD removal efficiency) over three cycles. Moreover, the effectiveness of this system was further demonstrated by treating stabilized landfill leachate, increasing the BOD5/COD ratio from 0.08 to 0.49.