Efficient catalytic reduction of methylene blue and p-Nitrophenol by CuNP/hydrochar nanocomposites synthesized from organic peel waste
Nora A. Hamad, Ahmed A. Galhoum, A. Saad, S. Wageh
Abstract
The study enhances waste-to-resource circularity by transforming orange peel waste into an efficient biocatalyst for wastewater remediation. The excessive industrial use of methylene blue (MB) and p -nitrophenol (PNP) generates hazardous wastewater, posing significant risks to ecosystems and public health. To address this, a spherical copper nanoparticle-decorated hydrochar nanocomposite (CuNP/HC) was developed from orange peel waste via hydrothermal reduction. Structural analysis via XPS analysis confirmed oxygen-functional groups (C–OH, C=O, –COO − ) and zero-valent copper on CuNP/HC surfaces, while XRD revealed highly crystalline Cu⁰ with a face-centered cubic (FCC) structure. The uniformly dispersed spherical CuNPs (10–20 nm) and hydrochar’s carbonaceous framework (evidenced by UV–Vis π-π*/n-π* transitions) endowed the nanocomposite with enhanced catalytic properties. CuNP/HC served as a biocatalyst for the degradation of anthropogenic pollutants (MB and PNP) using NaBH 4 , following pseudo-first-order kinetics. Under optimized conditions (including pollutant concentration, catalyst dosage, NaBH 4 concentration and pH), the apparent rate constants (k app ) were 0.1782 min −1 for PNP (30.58 µM, R 2 = 0.9982) and 0.1546 min −1 for MB (15.63 µM, R 2 = 0.9972), achieving complete degradation within 10.27 and 11.73 min, respectively. Notably, normalized rate constants (K app ) reached 19.44 g −1 s −1 (PNP) and 16.58 g −1 s −1 (MB) at maximal catalyst loading (CuNP/HC dosage), outperforming bare HC (free-CuNPs, via adsorption). The CuNP/HC nanocomposite demonstrated exceptional stability and sustained catalytic efficiency across multiple cycles, confirming scalability for wastewater remediation.