Photocatalytic Polyaromatic hydrocarbons (PAH) utilizing magnetic CrFe2O4 nanoparticle: Green synthesis, characterization, ab initio studies, electronic, magnetic features and water treatment application

Abstract

Polyaromatic hydrocarbons (PAHs) are priority pollutants due to their mutagenicity, persistence, and proven carcinogenicity. Consequently, we investigated the photooxidative degradation of prototypical toxic PAHs, namely anthracene (ANTH) and phenanthrene (PHEN), and naphthalene (NAPH) utilizing magnetic CrFe2O4 nanoparticles under visible light LED irradiation. The prepared nanoparticles, characterized by P-XRD, IR, and SEM, reveal a cubic (FCC) structure and an average particle size of 25.6 nm. On Ab initio study we employed spin polarized first-principle calculations using the Full-Potential Linearized Augmented Plane-Wave (FLAPW) method with GGA-mBJ potentials implemented in the Wien2k package to investigate the properties of CrFe2O4 spinel compound; the calculations reveal that CrFe2O4 adopts a cubic crystal structure with space group 227 (Fd-3 m), and exhibits semiconductor characteristics in both spin channels, featuring indirect band gaps of 1.12 eV (spin-up) and 0.43 eV (spin-down) at the Γ-L and K-Γ points, respectively. Furthermore, the material demonstrates ferromagnetic behavior, with a spin magnetic moment of 20 µB per unit cell. Optical spectra analysis concurs with band structure calculations, suggesting the suitability of this material for photovoltaic applications. The CrFe2O4 magnetic nanoparticles were synthesized through an eco-friendly approach using Boswellia carteri resin as a natural surfactant in an aqueous medium. Our synthesized materials exhibited excellent photocatalytic performance, leading to a rapid exponential decay of ANTH and PHEN over 3 h under visible LED light. The effect of different radical scavengers revealed the role of the percentage of active species OH, h+, and ˙O2− in the oxidation of selected PAHs. At neutral pH, the photo-degradation of PAHs (200 g L−1) by CrFe2O4 (10 mg) followed first-order kinetics and the Langmuir model (R2: 0.99). Exceptional degradation efficiencies were achieved, with ANTH exhibiting a removal efficiency of 99 %, PHEN of 90 %, and NAPH of 86 %. These results show the effectiveness of the synthesized materials as benign and environmentally friendly magnetic nanoparticles for removing carcinogenic PAHs, offering a sustainable, green, and reusable (n = 7) catalytic system to address this environmental challenge.