Abstract:In order to effective degradation of organic dye both under visible light or ultrasonic irradiation, the MWCNTs (multiwalled carbon nanotube) deposited with Fe and TiO2 were prepared by a modified sol-gel method. The Fe/TiO2-MWCNT catalyst was characterized by surface area of BET, scanning electron microscope (SEM), Transmission Electron Microscope (TEM), X-ray diffraction (XRD), and energy dispersive X-ray (EDX) and ultraviolet-visible (UV-vis) spectroscopy. The low intensity visible light and low power ultra… Show more
“…There were significant differences in crystallite sizes with increasing amounts of DWCNTs in the nanocomposites (Table 1). Similar studies on Fe/TiO 2 -MWCNT composites reported average crystallite size of 5 nm [29]. Optical properties of the nanocomposites are shown in Figure 4(a).…”
Double walled carbon nanotube (DWCNT)/N,Pd codoped TiO 2 nanocomposites were prepared by a modified sol-gel method and characterised using FTIR, Raman spectroscopy, TGA, DRUV-Vis, XRD, SEM, and TEM analyses. TEM images showed unique pearl-bead-necklace structured morphologies at higher DWCNT ratios. The nanocomposite materials showed characteristic anatase TiO 2 Raman bands in addition to the carbon nanotube D and G bands. Red shifts in the UV-Vis absorption edge were observed at low DWCNT percentages. The photocatalytic activity of DWCNT/N,Pd TiO 2 nanocomposite was evaluated by the photocatalytic degradation of eosin yellow under simulated solar light irradiation and the 2% DWCNT/N,Pd TiO 2 nanocomposite showed the highest photoactivity while the 20% DWCNT/N,Pd TiO 2 hybrid was the least efficient. The photocatalytic enhancement was attributed to the synergistic effects of the supporting and electron channeling role of the DWCNTs as well as the electron trapping effects of the platinum group metal. These phenomena favour the separation of the photogenerated electron-hole pairs, reducing their recombination rate, which consequently lead to significantly enhanced photoactivity.
“…There were significant differences in crystallite sizes with increasing amounts of DWCNTs in the nanocomposites (Table 1). Similar studies on Fe/TiO 2 -MWCNT composites reported average crystallite size of 5 nm [29]. Optical properties of the nanocomposites are shown in Figure 4(a).…”
Double walled carbon nanotube (DWCNT)/N,Pd codoped TiO 2 nanocomposites were prepared by a modified sol-gel method and characterised using FTIR, Raman spectroscopy, TGA, DRUV-Vis, XRD, SEM, and TEM analyses. TEM images showed unique pearl-bead-necklace structured morphologies at higher DWCNT ratios. The nanocomposite materials showed characteristic anatase TiO 2 Raman bands in addition to the carbon nanotube D and G bands. Red shifts in the UV-Vis absorption edge were observed at low DWCNT percentages. The photocatalytic activity of DWCNT/N,Pd TiO 2 nanocomposite was evaluated by the photocatalytic degradation of eosin yellow under simulated solar light irradiation and the 2% DWCNT/N,Pd TiO 2 nanocomposite showed the highest photoactivity while the 20% DWCNT/N,Pd TiO 2 hybrid was the least efficient. The photocatalytic enhancement was attributed to the synergistic effects of the supporting and electron channeling role of the DWCNTs as well as the electron trapping effects of the platinum group metal. These phenomena favour the separation of the photogenerated electron-hole pairs, reducing their recombination rate, which consequently lead to significantly enhanced photoactivity.
“…On the other hand, hydroxyl radicals generated via the sonocatalysis is easily transferred to the surface of the ZnO-biosilica nanocomposite, degrading the adsorbed MB molecules. In fact, the immobilized ZnO nanostructures create photoactive centers for the generation of e À /h + pair, whereas the biosilica supplies active adsorption sites in the vicinity of the sonocatalyst [28,30]. This enhances the potential of the sonocatalyst to efficiently adsorb both dye molecules and the light irradiation produced during the cavitation.…”
Section: The Contribution Of Each Process Involved In the Sonocatalysismentioning
confidence: 97%
“…With increasing the initial pH, the surface of the sonocatalyst will be deprotonated, enhancing the attraction force between the cationic dye and negatively charged sonocatalyst. As an another reason, the generation of OH Å radicals as a result of the reaction between the generated h + and OH À ions will be increased at basic conditions [28]. Besides, the sharp decrease in color removal (%) at strong acidic pH (pH = 3) may be due to the corrosion of the sonocatalyst in acidic conditions.…”
Section: Effect Of the Initial Phmentioning
confidence: 98%
“…In the case of ''sonoluminescence'' phenomenon, the ultrasonic irradiation may lead to the creation of the light irradiation with a wide wavelength range due to the cavitation [28], exciting the semiconductor to act as a photocatalyst for the generation of electron-hole pairs and subsequently, OH Å radicals as represented in the following equations [9]:…”
Section: The Contribution Of Each Process Involved In the Sonocatalysismentioning
In the present study, a porous clay-like support with unique characteristics was used for the synthesis and immobilization of ZnO nanostructures to be used as sonocatalyst for the sonocatalytic decolorization of methylene blue (MB) dye in the aqueous phase. As a result, the sonocatalytic activity of ZnO-biosilica nanocomposite (77.8%) was higher than that of pure ZnO nanostructures (53.6%). Increasing the initial pH from 3 to 10 led to increasing the color removal from 41.8% to 88.2%, respectively. Increasing the sonocatalyst dosage from 0.5 to 2.5 g/L resulted in increasing the color removal, while further increase up to 3g/L caused an obvious drop in the color removal. The sonocatalysis of MB dye over ZnO-biosilica nanocomposite was temperature-dependent. The presence of methanol produced the most adverse effect on the sonocatalysis of MB dye. The addition of chloride and carbonate ions had a negligible effect on the sonocatalysis, while the addition of persulfate ion led to increasing the color removal from 77.8% to 99.4% during 90 min. The reusability test exhibited a 15% drop in the color removal (%) within three consecutive experimental runs. A mineralization efficiency of 63.2% was obtained within 4h.
“…In the case of a nanosized Bi 2 Se 3 and TiO 2 nanocrystal line coupled graphene based photcatalyst system, coupling of two such semiconductors has a beneficial role in improving charge separation and extends TiO 2 in response to visible light compared with our previous experiment results. 34) A mechanism for the degradation of pollutants on a Bi 2 Se 3 coupled TiO 2 catalyst under visible light irradiation and ultrasonic irradiation is shown in Fig. 9.…”
This paper introduces a microwave-assisted synthesis method to prepare hybrid Bi 2 Se 3-GR/TiO 2 nanocomposites, which exhibit superior properties over single component materials. The as-prepared composites were characterized by XRD, UV-vis absorbance spectra, SEM,TEM, EDX, and BET analyses, revealing uniform covering of the graphene nanosheet with Bi 2 Se 3 and TiO 2 nanocrystals. For visible light photocatalysis of Rh.B, a significant enhancement in the reaction rate was consequently observed with Bi 2 Se 3-GR/TiO 2 composites. The degradation rate(k app) obtained for sonophotocatalysis was 6.8× 10-3 min-1 , roughly 2.2 times better than that of VL photocatalysis under higher concentrations of Rh.B. The sonophotocatalysis was faster due to greater formation of reactive radicals as well as an increase of the active surface area of the Bi 2 Se 3-GR/TiO 2 composites. The high activity is attributed to the synergetic effects of high charge mobility and red shift of the absorption edge of Bi 2 Se 3-GR/TiO 2 .
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