Facile synthesis of carbon supported ternary nickel-cobalt-iron nanocatalyst for the hydrodechlorination of 2-chlorophenol

Introduction: Chlorophenols (CPs) have become prevalent in the manufacture of herbicides, fungicides, pesticides, insecticides, pharmaceuticals, and dyes, contributing significantly to water pollution. Addressing this challenge, various treatment methods such as incineration, electrochemistry, photochemistry, biotechnology, and catalytic hydrodechlorination have been explored to reduce toxic chlorophenol contaminants. Hydrodechlorination stands out as an efficient technique for the removal of chlorine atoms. The dispersion of metal nanoparticles on supported materials significantly enhances the catalytic activity by increasing the specific surface area. Among these, carbon-supported nickel-cobalt-iron nanoparticles emerge as promising catalysts for the hydrodechlorination of 2-chlorophenol. Method: This study employs a chemical reduction method at high temperatures under an inert gas atmosphere to synthesize carbon-supported ternary nickel-cobalt-iron nanocatalysts, aiming to detoxify soil and water from pesticide residues. The physicochemical properties of these nanocatalysts were characterized using energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Their catalytic activity was assessed through gas chromatography with a flame ionization detector (FID). Results: The analysis revealed that metallic nanoparticles are uniformly dispersed on the carbon support, with particle sizes ranging from 10 to 60 nm and an average size of 30 nm. The hydrodechlorination (HDC) of 2-chlorophenol (2-CP) achieved satisfactory conversions under various reaction conditions. Conclusion: The carbon-supported nickel-cobalt-iron nanoparticles demonstrated effective catalytic activity for the hydrodechlorination of 2-chlorophenol, highlighting their potential for application in the treatment of chloroorganic contaminations in the future.