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Tailoring CuO-Fe₂O₃ nanocomposites via mechanochemical synthesis and calcination for efficient photocatalytic fluorescein removal

Maqsoom ZainDepartment of Chemistry, University of Azad Jammu and Kashmir, Muzaffarabad 13100, PakistanKhawaja Ansar YasinDepartment of Chemistry, University of Azad Jammu and Kashmir, Muzaffarabad 13100, PakistanSirajul HaqDepartment of Chemistry, University of Azad Jammu and Kashmir, Muzaffarabad 13100, PakistanShafia ShujaatDepartment of Chemistry, University of Azad Jammu and Kashmir, Muzaffarabad 13100, PakistanMohammad Khalid Al-SadoonDepartment of Zoology, College of Science, King Saud University, PO Box 2455, Riyadh 11451, Saudi ArabiaJamoliddin RazzokovDepartment of Biotechnology, Tashkent State Technical University, Universitet 2, Tashkent 100095, UzbekistanAhsan EjazDepartment of Physics, University of Kotli Azad Jammu and Kashmir, Kotli 11100, Pakistan
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Аннотация

The Copper Oxide-Iron Oxide Nanocomposites (CuO-Fe 2 O 3 NCs) were fabricated via simple grinding process using mortar and pestle and were then subjected for calcination at 300, 600, and 900 °C for 3 h. Various physicochemical techniques including X-ray diffraction (XRD), energy dispersive X-rays (EDX), Fourier Transform Infrared (FTIR) spectroscopy, scanning electron microscopy (SEM), diffuse reflectance spectroscopy (DRS) and N 2 adsorption were employed to analyze the physicochemical properties of CuO-Fe 2 O 3 NCs. It has been observed that the calcination temperature greatly affected the sample crystallinity, morphological features, band gap energy, chemical composition and surface area of the CuO-Fe 2 O 3 NCs. The particles size and crystallinity of the samples increases with increasing calcination temperature whereas as the surface area has an inverse relation with calcination temperature. To degrade fluorescein, the fabricated NCs were utilized as photocatalyst under solar light irradiation. The temperature induced structural and optical variations had strong impact on the photocatalytic behavior of the samples and the activity was seen to decrease with increasing calcination temperature. The highest activity (88.95 %) was recorded for uncalcined sample. Moreover, the effect of initial dye concentration, catalyst dose, and pH along with recycling stability of the catalysts was studied.

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