rGO-WO[sub.3] Heterostructure: Synthesis, Characterization and Utilization as an Efficient Adsorbent for the Removal of Fluoroquinolone Antibiotic Levofloxacin in an Aqueous Phase

Herein, the heterostructure rGO-WO[sub.3] was hydrothermally synthesized and characterized by HRTEM (high-resolution transmission electron microscopy), FESEM (field emission scanning electron microscopy), XRD (X-ray diffraction), FT-IR (Fourier transform infrared spectroscopy), XPS (X-ray photoelect...

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2022-10, Vol.27 (20)
Hauptverfasser: Kaur, Manjot, Singh, Shafali, Mehta, Surinder Kumar, Kansal, Sushil Kumar
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Sprache:eng
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Zusammenfassung:Herein, the heterostructure rGO-WO[sub.3] was hydrothermally synthesized and characterized by HRTEM (high-resolution transmission electron microscopy), FESEM (field emission scanning electron microscopy), XRD (X-ray diffraction), FT-IR (Fourier transform infrared spectroscopy), XPS (X-ray photoelectron microscopy), nitrogen physisorption isotherm, Raman, TGA (thermogravimetric analysis) and zeta potential techniques. The HRTEM and FESEM images of the synthesized nanostructure revealed the successful loading of WO[sub.3] nanorods on the surface of rGO nanosheets. The prepared heterostructure was utilized as an efficient adsorbent for the removal of a third-generation fluoroquinolone antibiotic, i.e., levofloxacin (LVX), from water. The adsorption equilibrium data were appropriately described by a Langmuir isotherm model. The prepared rGO-WO[sub.3] heterostructure exhibited a Langmuir adsorption capacity of 73.05 mg/g. The kinetics of LVX adsorption followed a pseudo-second-order kinetic model. The adsorption of LVX onto the rGO-WO[sub.3] heterostructure was spontaneous and exothermic in nature. Electrostatic interactions were found to have played a significant role in the adsorption of LVX onto the rGO-WO[sub.3] heterostructure. Thus, the prepared rGO-WO[sub.3] heterostructure is a highly promising material for the removal of emerging contaminants from aqueous solution.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules27206956