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Md. Abdul Gafur

Publications and source records attributed to Md. Abdul Gafur.

2 recordsLinked to original sources

Effect of Dissolved Oxygen Content on Photocatalytic Performance of Graphene Oxide

Graphene, a two-dimensional (2D) promising emergent photocatalyst consisting of earth-abundant elements. This study evaluated the potential of graphene oxide (GO) towards photocatalytic degradation of a novel organic dye, Methylene Blue (MB). In this work, photocatalytic activity of graphene oxide (GO), graphene oxide (GO) along with hydrogen peroxide (H2O2) were tested by photodegrading Methylene Blue (MB) in aqueous solution. The resulted GO nanoparticles were characterized by X-ray powder diffraction, Scanning Electron Microscopy, Energy Dispersive Spectroscopy and Fourier Transform Infrared Ray Spectroscopy. The XRD data confirms the sharp peak centered at 2Theta=10.44 degree corresponding to (002) reflection of GO. Based on our results, it was found that the resulted GO nanoparticles along with H2O2 achieved ~92% photodecolorization of MB compared to ~63% for H2O2 under natural sunlight irradiation at pH~7 in 60 min. The influences of oxygen and hydrogen peroxide (H2O2) on the degradation of MB during sunlight/GO process were investigated. Experimental results indicated that oxygen was a determining parameter for promoting the photocatalytic degradation. The rate constant of degradation (k1) increased from 0.019 to 0.042 per minute for dissolved oxygen content (DOC) 3.5 mg/L when direct photocatalysis (MB/GO) and H2O2-assisted photocatalysis (MB/H2O2/GO) were used. Owing to the fact that H2O2 acted as an electron and hydroxyl radicals scavenger, the addition of H2O2 should in a proper dosage to enhance the degradation of MB. Moreover, as the initial concentration of dissolved oxygen (DO) was increased from 2.8 to 3.9 mg/L, the rate constant of degradation (k1) increased from 0.035 to 0.062 per minute. The mechanism of photodegradation and kinetics were also studied for both direct photocatalysis and H2O2-assisted photocatalysis.

cond-mat.mtrl-sci↗

Significantly enhanced photocatalytic degradation of Methylene Blue using rGO-SnO2 nanocomposite under natural sunlight and UV light irradiation

In this paper, we report the synthesis of reduced Graphene Oxide-Tin Oxide nanocomposite and the effectiveness of this composite in decolorizing and degrading Methylene Blue (MB). Tin Oxide was prepared by liquid phase co-precipitation method and reduced Graphene Oxide-Tin Oxide (rGO-SnO2) nanocomposite was prepared by solution mixing method. Tin Oxide nanoparticles (NPs) have been ardently investigated as photocatalyst for water purification and environment decontamination but the photon generated electron and hole pair (EHP) recombination is one of the limiting factors. Reduced Graphene Oxide-Tin Oxide (rGO-SnO2) nanocomposite is very efficient to overcome this limitation for photocatalytic application. The as-synthesized GO, SnO2, GO-SnO2, rGO and rGO-SnO2 nanocomposite were characterized by X-ray Diffraction, Scanning Electron Microscopy, Energy Dispersive X-ray spectroscopy and Fourier Transform Infrared spectroscopy. The XRD data confirms the sharp peak at 2Theta=10.44 degree corresponding to (002) reflection of GO with interlayer d spacing of 8.46 Angstrom indication of successful preparation of GO by oxidation of graphite. Moreover, the diffraction peak shifts from 2Theta=10.44 degree to 2Theta=23.31 degree confirm successful synthesis of rGO as well. SEM image shows the morphology of all the photocatalysts. EDX studies are carried out to investigate the elemental composition and purity of the sample by giving all the elements present in the nanomaterials. The presence of functional groups was identified by FTIR. The rGO-SnO2 (1:10) nanocomposite shows an efficient photodegradation efficiency of ~94% and ~95% under natural sunlight and UV light irradiation respectively for Methylene Blue (MB) within 15 minutes. Furthermore, the degradation kinetics of MB is also studied in this paper as well.

physics.app-ph↗