Pharmaceutical effluent degradation using hydrogen peroxide-supported zerovalent iron nanoparticles catalyst.

Autor: Imohiosen FA; Department of Chemical Sciences, Mountain Top University, Pakuro, Ogun State, Nigeria., Ofudje EA; Department of Chemical Sciences, Mountain Top University, Pakuro, Ogun State, Nigeria. eaofudje@mtu.edu.ng., Al-Ahmary KM; Department of Chemistry, College of Science, University of Jeddah, Jeddah, Saudi Arabia., Al-Mhyawi SR; Department of Chemistry, College of Science, University of Jeddah, Jeddah, Saudi Arabia., Alshdoukhi IF; Department of Basic Sciences, College of Science and Health Professions, King Saud bin, Abdulaziz University for Health Science, King Abdullah International Medical Research Center, Riyadh, Saudi Arabia., Alrahili MR; Physics Department, School of Science, Taibah University, Medina, 42353, Saudi Arabia., Alsaiari AA; Department of Clinical Laboratory Science, College of Applied Medical Science, Taif University, Taif, Saudi Arabia., Din SU; Department of Chemistry, University of Azad Jammu and Kashmir, Muzaffarabad, 13100, Pakistan.
Jazyk: angličtina
Zdroj: Scientific reports [Sci Rep] 2024 Oct 14; Vol. 14 (1), pp. 23957. Date of Electronic Publication: 2024 Oct 14.
DOI: 10.1038/s41598-024-74627-7
Abstrakt: Pharmaceutical effluents generated during drugs production and application are often times released into the water systems with little or no treatment, which could pose potential danger to the ecosystem. Advanced oxidation processes for organic pollutants treatment have gained wide consideration due to their effectiveness. In this work, hydrogen peroxide (H 2 O 2 ) and hydrogen peroxide-supported nano zerovalent iron (H 2 O 2 @nZVIs) were deployed to study pharmaceutical effluents (PE) degradation via batch experiments, under various reaction time, (H 2 O 2 ) and (H 2 O 2 @nZVIs) concentrations, pH, PE concentration, and temperature. The nZVIs was prepared from the green synthesis of Vernonia amygdalina leaf extract and characterized using different analytical tools such as Fourier Transform-Infrared Spectroscopy (FT-IR), Gas Chromatography Mass Spectroscopy (GC-MS), Scanning Electron Microscopy (SEM), and X-Ray Diffraction Spectroscopy (XRD). The FT-IR results showed the presence of -C = O, -NH, -OH, -C = C and, -C-O functional groups, SEM report showed that the morphology of the nZVIs is round in shape, while GC-MS revealed the presence of several phytochemicals. When the concentration of the effluent was increased from 10 to 30 ml, the percentage decolourization decreased from 74.74 to 51.96% and from 80.36 to 54.38% for H 2 O 2 and H 2 O 2 @nZVI respectively, whereas when the contact time was increased from 10 to 60 min, the percentage decolourization rose from 70.39 to 83.49% for H 2 O 2 and from 85.19 to 89.73% when H 2 O 2 @nZVI was used. When the effect of pH was assessed, it was observed that on increasing the pH from 2 to 10, the percentage decolourization rose from 74.5 to 80.25% for H 2 O 2 , however, with H 2 O 2 @nZVI, the percentage decolourization decreased from 81.50 to 68%. Maximum percentage decolourization of 57.10% and 94.56% for H 2 O 2 and H 2 O 2 @nZVI was achieved at catalyst volume of 25 ml. For all the parameters tested, the H 2 O 2 @nZVIs performed much better indicating that the nZVIs enhanced the decolourization ability of the H 2 O 2 . The kinetic results showed that the decolorization of pharmaceutical effluent by both catalysts fitted very well with the second-order model, while thermodynamic properties of enthalpy change were found to be 10.025 and 27.005 kJ/mol/K for H 2 O 2 and H 2 O 2 @nZVIs respectively suggesting that the oxidation process is endothermic in nature. This technique employed in using hydrogen peroxide-supported zero valent iron, proved to be highly efficient not only for pharmaceutical effluent degradation but also in the elimination of lead from the effluent.
(© 2024. The Author(s).)
Databáze: MEDLINE
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