The present work mainly aimed to synthesize different weight percentages (0.25–1.00 wt%) of Manganese (Mn2+) and Magnesium (Mg2+) bimetal ions doped TiO2 nanomaterial assisted with different weight percentages (5–15 wt%) of Gemini surfactant (GS) using sol-gel method. The bimetal doped and undoped TiO2 photocatalysts were characterized by X-ray Diffraction, Scanning Electron Microscopy, Energy Dispersive X-ray Spectroscopy, Fourier Transform Infrared Spectroscopy (FT-IR), UV-Visible Diffused Reflectance Spectroscopy, Transmission Electron Microscopy, Brunauer-Emmett-Teller surface area analyzer, and Photoluminescence Spectroscopy. Characterization results revealed that mesoporous multi-particle anatase TiO2 nanoparticles with a narrowed band gap, small particle size, and high surface area were formed due to the combined effect of Mn2+/Mg2+ bimetal ions doping and effective encapsulation of GS over the initially formed TiO2 nanoparticles. The surface elemental composition of the 0.25 wt% Mn2+ and 1.00 wt% Mg2+ bimetal doped TiO2 in the presence of 10 wt% of GS (after calcination) revealed the presence of both the metal dopants Mn2+ and Mg2+ along with the Ti and O and their chemical interactions were further confirmed by FT-IR results. The photocatalytic activity of these catalysts was assessed by the degradation of Methyl Red using visible light irradiation. To understand the effect of different reaction parameters on the photocatalytic activity of the nanocatalysts such as the dopant concentration, surfactant concentration, catalyst dosage, solution pH, and initial dye concentration were investigated and optimized to achieve the best performance. The photoluminescence results conclude that OH radicals are the crucial reactive species responsible for oxidative photocatalytic degradation of Methyl Red.
The present investigation aimed to design a best performing improved photocatalytic-active material of extensive implications and suitable to achieve the emerging needs of water pollution abatement. In view of the above, the present research work planned to synthesized nickel and phosphorus double-doped TiO 2 (NPT's) by the sol-gel process, characterized by advanced instrumental techniques and applied for the abatement of methylene blue (MB) under visible light. Characterization results demonstrated that nickel and phosphorus co-doped TiO 2 samples showed anatase phase determined by XRD. Structural aspects such as smooth surface with spherical shape morphology, less band gap, less particle size, and high surface area when compared with bare TiO 2 were determined by SEM, UV-Vis. DRS, TEM and BET, respectively. The elemental composition and oxidation states were identified by XPS analysis. The substitutional doping of Ti 4+ ion by Ni 2+ , P 5+ ion and P 3− ion with oxygen in the TiO 2 lattice was evaluated by FT-IR spectroscopy. Based on the characterization results, the catalyst NPT5 was applied for the abatement of MB at various optimum reaction conditions, with pH 10, catalyst weight 0.1 g/l and starting MB concentration 10 mg/l. At these reaction conditions, the degradation was completed within 75 min in the visible light. The photostability of the NPT5 was verified by recycling up to five cycles. Finally, this research work was concluded with a plausible mechanism, using reactive species generated during the degradation process and these species were simultaneously tested using scavenger reagents.
The present work mainly aimed to synthesize different weight percentages (0.25-1.00 wt%) of Manganese (Mn2+) and Magnesium (Mg2+) bimetal ions doped TiO2 nanomaterial assisted with different weight percentages (5-15 wt%) of Gemini Surfactant (GS) using sol-gel method. The bimetal doped and undoped TiO2 photocatalysts were characterized by X-ray Diffraction, Scanning Electron Microscopy, Energy Dispersive X-ray Spectroscopy, Fourier Transform Infrared Spectroscopy (FT-IR), UV-Visible Diffused Reflectance Spectroscopy, Transmission Electron Microscopy, Brunauer-Emmett-Teller surface area analyzer, and Photoluminescence Spectroscopy. Characterization results revealed that mesoporous multi-particle anatase TiO2 nanoparticles with a narrowed band gap, small particle size, and high surface area were formed due to the combined effect of Mn2+/Mg2+ bimetal ions doping and effective encapsulation of GS over the initially formed TiO2 nanoparticles. The surface elemental composition of the 0.25 wt% Mn2+& 1.00 wt% Mg2+ bimetal doped TiO2 in presence of 10 wt% of Gemini surfactant (after calcination) revealed the presence of both the metal dopants Mn2+ and Mg2+ along with the Ti and O and their chemical interactions were further confirmed by FT-IR results. The photocatalytic activity of these catalysts was assessed by the degradation of Methyl Red (MR) using visible light irradiation. To understand the effect of different reaction parameters on the photocatalytic activity of the nanocatalysts such as the dopant concentration, GS concentration, catalyst dosage, solution pH, and initial dye concentrations were investigated and optimized to achieve the best performance. The photoluminescence results conclude that OH radicals are the crucial reactive species responsible for oxidative photocatalytic degradation of MR.
Photocatalyst has been extensive interest because of it’s new innovation to the reduce the contamination in the environment. A straight forward and economical procedure has been employed by sol-gel technique for the co-doping of Mn2+ and Ni2+ into TiO2 . The co-doped and undoped photocatalysts were described by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Energy dispersive X-ray Spectroscopy (EDX), Fourier transform infrared spectroscopy (FT-IR), UV-Visible Diffused Reflectance Spectroscopy (UV Vis-DRS), Transmission electron Microscopy (TEM) and Brunauer-Emmett-Teller (BET). The portrayal results shows that anatase and rutile mixed phase was observed for some co-doped nanocatalysts and the remaining catalysts exhibits anatase phase only. It was observed by FT-IR that the shifting of frequency of Ti-O-Ti in the catalysts was seen due to substitutional doping of Mn and Ni by replace Ti and O, further the photocatalysts shows rough morphology, irregular shape of particle with size (6.5nm) and having high surface area (135.70 m2/g), less band energy (2.7 eV). The photocatalytic action of these materials was assessed by the degradation of Allura red (AR) as a contaminant. The results shows that AR has degraded within 60 minutes at doping concentrations 0.25 Wt% of Mn2+ion and 1.0 Wt% of Ni2+ ion in TiO2 (NMT2) at an optimum reaction parameters pH-4, catalyst dose 0.070g/L and at AR initial dye concentration 0.010g/L.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.