Abstract

ABSTRACT Co-precipitation was employed to synthesize copper-based layered double hydroxides, which were subsequently utilized as heterogeneous catalysts for the ozonation of 4-nitrophenol in aqueous solutions. Various analytical techniques, including X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA), were utilized to characterize CuAl-CO3 and CuAl500.The catalytic activity of CuAl-CO3 was evaluated under different reaction conditions. Notably, at pH 11 and 25 °C, CuAl-CO3 exhibited high catalytic efficiency in the ozonation of 4NP. Increasing the catalyst dose, initial pH, and temperature led to enhanced 4NP degradation. An optimal pH of 11 and a catalyst dose of 0.3 g. L−1 resulted in the removal of 78.6% of the initial 4NP concentration. Additionally, ozonation proved to be more efficient at temperatures of 10 °C and 55 °C. The kinetics of 4NP ozonation over CuAl-CO3 and CuAl500 followed a pseudo-first-order reaction. Furthermore, the study demonstrated that CuAl-CO3 and CuAl500 exhibited stability and repeatability across multiple reaction cycles, highlighting their potential for continuous catalytic applications. Overall, this research emphasizes the effectiveness of CuAl-CO3 and CuAl500 as reliable heterogeneous catalysts for the ozonation of 4NP. The results contribute valuable insights into the development of advanced oxidation processes for the treatment of wastewater containing organic contaminants.

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