AI Article Synopsis

  • Antibiotics in water and waste raise serious environmental and health issues, prompting the need for effective removal strategies focused on pollutants like cephalexin (CPX).
  • Researchers created a spinning disc photoreactor (SDPR) with a ZnO/Ag/WO photocatalyst to enhance CPX degradation using blue light, achieving a high degradation efficiency of 98.8%.
  • The study highlighted the advantages of this setup, including improved light absorption, mass transfer, and effective radical species involvement, confirming the efficacy and potential for reusability of the developed photocatalyst.

Article Abstract

The presence of antibiotics in wastes and drinking water has led to serious environmental and health concerns, further necessitating the development of an advanced sustainable strategy to eliminate antibiotics from aquatic media. In this context, the present research reports the successful fabrication of a spinning disc photoreactor (SDPR) supported ZnO/Ag/WO S-scheme visible-light-driven thin-film photocatalyst to study the degradation of cephalexin (CPX) as a target pollutant under blue light irradiation. The optical, electrochemical and physicochemical characterization of the as-prepared thin-film samples were carried out by XRD, top-view FE-SEM, EDS-mapping, UV-Vis-DRS, contact angle, EIS, transient photocurrent, mott Schottky and AFM techniques. The rod shape morphology of the samples with moderate surface roughness, desirable hydrophobicity, low bandgap and remarkable band structure alignment confirmed the applicability of as-prepared thin-film with an average photon flux of 1.94 × 10-8.61 × 10 E's m s. The use of a rotating catalytic disc impressively declined the photon propagation distance, decremented the probability of light absorption by the solution, and intensified the mass transfer rate. The maximum throughputs of 98.8% efficiencies for CPX degradation were achieved at a rotational speed of 180 rpm, the solution flow rate of 1.0 L min, the light intensity of 11 mW cm, and initial CPX concentration of 40 mg L, illumination time of 80 min, and pH of 6. Damkohler number (Da) value was found to be 1.23 × 10 at the optimum conditions, indicating the negligibility of the external mass transfer resistance in the SDPR. The photocatalytic mechanism was elucidated for finding the most operative radical species, suggesting the crucial role of ·O in photodegradation of CPX and a drastic improvement of the charge separation by S-scheme heterostructure and facilitation by Ag mediator. Findings indicated that the developed reusable and robust SDPR benefited from an s-scheme photocatalyst can be a promising technology for degradation of the organic compounds.

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http://dx.doi.org/10.1016/j.chemosphere.2022.135812DOI Listing

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