scholarly journals Gemini surfactant assisted synthesis of mesoporous Mn/Mg bimetal doped TiO2 nanomaterial: characterization and photocatalytic activity studies under visible light irradiation

2021 ◽  
Vol 31 (1) ◽  
Author(s):  
Sankara Rao Miditana ◽  
Siva Rao Tirukkovalluri ◽  
Imandi Manga Raju ◽  
Shaik Abdul Alim ◽  
Genji Jaishree ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Surface Area ◽  
Visible Light Irradiation ◽  
Gemini Surfactant ◽  
Light Irradiation ◽  
Methyl Red ◽  
X Ray ◽  
Ft Ir

AbstractThe 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.

scholarly journals Gemini surfactant assisted synthesis of mesoporous Mn/Mg bimetal doped TiO2 nanomaterial: Characterization and photocatalytic activity studies under visible light irradiation

2021 ◽  
Author(s):  
Sankara Rao Miditana ◽  
Siva Rao Tirukkovalluri ◽  
Imandi Manga Raju ◽  
Shaik Abdul Alim ◽  
Genji Jaishree ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Surface Area ◽  
Visible Light Irradiation ◽  
Gemini Surfactant ◽  
Light Irradiation ◽  
Methyl Red ◽  
X Ray ◽  
Ft Ir

Abstract 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 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 Methyl Red.

scholarly journals Gemini surfactant abetted synthesis of mesoporous Mn/Mg bimetal doped TiO2 nanomaterial: Characterization and photocatalytic activity studies under visible light irradiation

2020 ◽  
Author(s):  
Sankara Rao Miditana ◽  
Siva Rao Tirukkovalluri ◽  
Imandi Manga Raju ◽  
Shaik Abdul Alim ◽  
Genji Jaishree ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Surface Area ◽  
Visible Light Irradiation ◽  
Gemini Surfactant ◽  
Light Irradiation ◽  
Oh Radicals ◽  
X Ray ◽  
Ft Ir

Abstract 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 evinced that Mn2+/Mg2+ bimetal ions doping and encapsulation of GS on TiO2 nanoparticles promote the formation of mesoporous multi-particle anatase TiO2 nanocatalysts with a narrowed band gap, less particle size, and high surface area. 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.

scholarly journals Gemini surfactant assisted synthesis of mesoporous Mn/Mg bimetal doped TiO2 nanomaterial: Characterization and photocatalytic activity studies under visible light irradiation

2020 ◽  
Author(s):  
Sankara Rao Miditana ◽  
Siva Rao Tirukkovalluri ◽  
Imandi Manga Raju ◽  
Shaik Abdul Alim ◽  
Genji Jaishree ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Surface Area ◽  
Visible Light Irradiation ◽  
Gemini Surfactant ◽  
Light Irradiation ◽  
Oh Radicals ◽  
X Ray ◽  
Ft Ir

Abstract 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.

scholarly journals Synthesis, Characterization and Photocatalytic Performance of Poly-3-Thenoic Acid/Cu-TiO2 Nanohybrid for Efficient Visible Light Assisted Degradation of Bismarck Brown R

2022 ◽  
Vol 19 (1) ◽  
pp. 1715
Author(s):  
Imandi Manga Raju ◽  
Tirukkovalluri Siva Rao ◽  
Miditana Sankara Rao
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Surface Area ◽  
Visible Light Irradiation ◽  
Sol Gel ◽  
Anatase Tio2 ◽  
X Ray ◽  
Ft Ir ◽  
Nanohybrid Material

The present work reported on the synthesis and characterization of Poly-3-Thenoic acid/Cu-TiO2 nanohybrid (PCuT) for the photocatalytic degradation of organic azo dye pollutant from wastewater. The as-synthesized nanohybrid by an in-situ modified sol-gel method including chemical oxidative polymerization was characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, UV-visible diffuse reflectance spectroscopy (UV-vis.DRS), scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDX), transmission electron microscopy (TEM) and Brunauer-Emmet-Teller (BET) surface area analysis. The characterization results revealed the formation of small aggregates of polymer contained high crystalline anatase TiO2 nanoparticles (XRD) with narrowed bandgap energy (UV-vis.DRS), decreased particle size (TEM) with smooth surface morphology (SEM) and large surface area (BET). All the constituent elements of the polymer and Cu-TiO2 were found in the PCuT nanohybrid material (EDX) and their chemical interaction studied by FT-IR confirmed the stability of the nanohybrid. The photocatalytic activity of the nanohybrid was tested by the degradation of Bismarck Brown R dye under visible light irradiation. To enhance the photocatalytic efficiency, effects of various catalyst/dye reaction parameters such as polymer content, solution pH, catalyst dosage, and initial dye concentration were studied and optimized. HIGHLIGHTS Poly-3-Thenoic acid/Cu-TiO2 nanohybrid material was successfully synthesized by in situ modified sol-gel process Poly-3-Thenoic acid has enhanced the visible light absorption capacity of anatase TiO2 in nanohybrids Electron-hole recombination in TiO2 was effectively inhibited by Cu doping Bismark Brown R, an organic pollutant was successfully degraded in 75 min of visible light irradiation GRAPHICAL ABSTRACT

A simple method to synthesise Ag-doped TiO2 photocatalysts with different Ag0:Ag2O atomic ratios for enhancing visible-light photocatalytic activity

2017 ◽  
Vol 41 (8) ◽  
pp. 475-483 ◽  
Author(s):  
C. Chen ◽  
X. F. Lei ◽  
M. Z. Xue
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Light Absorption ◽  
Separation Efficiency ◽  
Visible Region ◽  
Light Irradiation ◽  
Electron Hole ◽  
X Ray

Pure anatase TiO2 photocatalysts with different Ag contents were prepared via a simple sol-gel method. The as-prepared anatase Ag-doped TiO2 photocatalysts were characterised by X-ray diffraction, transmission electron microscopy, UV-Vis diffuse reflectance spectra, photoluminescence spectroscopy, X-ray photoelectron spectroscopy, thermal gravity and differential thermal analysis, scanning electron microscopy and N2 adsorption–desorption measurements (BET). Compared with pure TiO2, Ag-doped anatase TiO2 photocatalysts exhibited not only increases in light absorption in the visible region, the separation efficiency of electron–hole pairs and surface area, but also inhibition of the titania phase transition from anatase to rutile. Photoreduction results showed that Ag-doped anatase TiO2 photocatalysts have greatly improved photocatalytic activity, compared with pure TiO2, and the reduction of Cr(VI) under visible light irradiation was much higher than that of pure TiO2. The optimum Ag content was 1.0 mol%, which led to the complete reduction of Cr(VI) under visible light irradiation (λ > 420 nm) for 4 h. The enhanced photocatalytic activity was attributed to the synergic effect of the pure anatase structure, and the increased light absorption in the visible region, separation efficiency of electron–hole pairs and atomic ratio of Ag0:Ag2O.

scholarly journals Gemini Surfactant Abetted Synthesis Of Mesoporous Mn/Mg Bimetal Doped TiO2 Nanomaterial: Characterization And Photocatalytic Activity Studies Under Visible Light Irradiation

2020 ◽  
Author(s):  
Sankara Rao Miditana ◽  
Siva Rao Tirukkovalluri ◽  
Imandi Manga Raju ◽  
Shaik Abdul Alim ◽  
Genji Jaishree ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Gemini Surfactant ◽  
High Surface ◽  
Sol Gel ◽  
Light Irradiation ◽  
Oh Radicals ◽  
Solution Ph ◽  
Ft Ir

Abstract The present work mainly aimed to synthesize different weight percentages (0.25 Wt% - 1.00 Wt%) of Manganese (Mn2+) and Magnesium (Mg2+) bimetal ions doped TiO2 nanomarerial assisted with different weight percentages (5 Wt% - 15 Wt%) of Gemini Surfactant (GS) using sol-gel method. The bimetal doped and undoped TiO2 photocatalysts were characterized by XRD, SEM, EDX, FT-IR, UV Vis-DRS, TEM, BET and PL. Characterization results evinced that Mn2+/Mg2+ bimetal ions doping and encapsulation of GS on TiO2 nanoparticles promote the formation of mesoporous multi-particle anatase TiO2 nanocatalysts with narrowed band gap, less particle size and high surface area. The surface elemental composition of the MMT5-GS2 (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 best performance. The photoluminescence results conclude that OH radicals are the crucial reactive species responsible for oxidative photocatalytic degradation of MR.

Structure and Photocatalytic Activity of Nitrogen-doped HTiNbO5 Nanosheet Aggregation

NANO ◽  
2017 ◽  
Vol 12 (01) ◽  
pp. 1750003 ◽  
Author(s):  
Wei Lv ◽  
Jie He ◽  
Andong Xu ◽  
Lifang Hu ◽  
Liangguo Da
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Diffuse Reflectance Spectroscopy ◽  
Proton Exchange ◽  
Light Irradiation ◽  
Laser Raman Spectroscopy ◽  
X Ray ◽  
Nitrogen Doped

Nitrogen-doped HTiNbO5 nanosheet (N-HTiNbO5-NS) aggregation was successfully obtained through a series of process, including preparation of nitrogen-doped precursor (N-KTiNbO5), proton-exchange of N-KTiNbO5 and exfoliation of N-HTiNbO5. The structures of the as-prepared samples are characterized by means of powder X-ray diffraction (XRD), Scan electron microscopy (SEM), Transmission electron microscopy (TEM), N2 adsorption-desorption isotherms UV-visible diffuse reflectance spectroscopy (UV-Vis-DRS), Laser Raman spectroscopy (LRS), X-ray photoelectron spectroscopy (XPS) and Thermogravimetric analysis-differential scanning calorimetry (TG-DSC). The catalytic activities of the as-prepared samples are evaluated by the photocatalytic degradation of methylene blue (MB) aqueous solution under visible light irradiation. The results reveal that N-HTiNbO5-NS due to the large specific surface area and brilliant visible light response exhibits a relatively excellent photocatalytic activity in the decomposition of MB under visible light irradiation.

scholarly journals Direct Exfoliation of g-C3N4 with Addition of NaOH for Enhanced Photocatalytic Cr(Ⅵ) Reduction

2018 ◽  
Author(s):  
Yaping Guo ◽  
Jianyang Sun ◽  
Hui Chang ◽  
Xu Zhao
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Light Irradiation ◽  
X Ray Diffraction ◽  
Physiochemical Properties ◽  
X Ray ◽  
Transmission Electron ◽  
Ultrasonic Process

A simple, effective and environmental-friendly method was adopted for enhancing the photocatalytic activity of g-C3N4 in the reduction of aqueous Cr(Ⅵ) under visible-light irradiation. The enhancement was achieved via treatment of g-C3N4 in organic solvent with addition of NaOH particles by ultrasonic process for two hours. The results demonstrated that the treated g-C3N4 exhibited much higher photocatalytic activity than pristine g-C3N4 in the reduction of Cr(VI) . Under visible light irradiation for 120 min, the reduced ratios of Cr(VI) with the initial concentration of 50 mg/L in the presence of the treated g-C3N4and pristine g-C3N4 were 100% and 37.1%, respectively. With the addition of fulvic acid, Cr(VI) was efficiently removed at 40 min. Based on the characterization results of the structures and other physiochemical properties of the treated g-C3N4 and pristine g-C3N4 by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and UV Vis diffuse reflectance, the possible reasons responsible for the enhanced photocatalytic activity of the treated g-C3N4 were proposed. The yield and mechanism of different exfoliation methods were compared by semi-quantitative method.

scholarly journals Synthesis of Ag3PO4 using Hydrophylic Polymer and Their Photocatalytic Activities under Visible Light Irradiation

2017 ◽  
Vol 12 (2) ◽  
pp. 206 ◽  
Author(s):  
Uyi Sulaeman ◽  
Bin Liu ◽  
Shu Yin ◽  
Tsugio Sato
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Visible Light Irradiation ◽  
Photoelectron Spectroscopy ◽  
Light Irradiation ◽  
X Ray ◽  
Photocatalytic Activities

The highly active Ag3PO4 photocatalysts were successfully synthesized using the hydrophylic polymer of PVA (polyvinyl alcohol), PEG (polyethylene glycol) and PVP (polyvinyl pyrrolidone). The products were characterized using X-ray diffraction (XRD), Diffuse reflection spectroscopy (DRS), Field emission scanning electron microscope (FE-SEM), Brunauer–Emmett–Teller (BET) specific surface area, and X-ray photoelectron spectroscopy (XPS). Photocatalytic activities were evaluated using decomposition of Rhodamine B (RhB) under visible light irradiation. The results showed that the PVA, PEG, and PVP increased the specific surface area and enhanced the photocatalytic activity of Ag3PO4. The highest photocatalytic activity could be observed in Ag3PO4 synthesized with PVA, mainly due to an increase in electron excitation induced by PVA chemically adsorbed on the surface. Copyright © 2017 BCREC Group. All rights reservedReceived: 13rd November 2016; Revised: 10th February 2017; Accepted: 10th February 2017How to Cite: Sulaeman, U., Liu, B., Yin, S., Sato, T. (2017). Synthesis of Ag3PO4 using Hydrophylic Polymer and Their Photocatalytic Activities under Visible Light Irradiation. Bulletin of Chemical Reaction Engineering & Catalysis, 12 (2): 206-211 (doi:10.9767/bcrec.12.2.767.206-211)Permalink/DOI: http://dx.doi.org/10.9767/bcrec.12.2.767.206-211 

scholarly journals Synthesis of Nitrogen-Doped ZnS with Camellia Brushfield Yellow Nanostructures for Enhanced Photocatalytic Activity under Visible Light Irradiation

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Gang-Juan Lee ◽  
Chi-Lun Hong ◽  
Valentina Batalova ◽  
Gennady Mokrousov ◽  
Jerry Wu
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Photoelectron Spectroscopy ◽  
Light Irradiation ◽  
X Ray ◽  
Nitrogen Doped ◽  
Composite Catalysts ◽  
N Doping

Nitrogen modified zinc sulfide photocatalysts were successfully prepared and characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), high-resolution transmission electron microscopy (HR-TEM), X-ray photoelectron spectroscopy (XPS), and surface area analysis. Thermal decomposition of the semisolid was carried out under nitrogen conditions at 500°C for 2 hours, and a series of nitrogen-doped ZnS photocatalysts were produced by controlling inflow flow rate of nitrogen at 15–140 mL/min. Optical characterizations of the synthesized N-doping ZnS substantially show the shifted photoabsorption properties from ultraviolet (UV) region to visible light. The band gaps of nitrogen-doped ZnS composite catalysts were calculated to be in the range of 2.58~2.74 eV from the absorptions edge position. The 15N/ZnS catalyst shows the highest photocatalytic activity, which results in 75.7% degradation of Orange II dye in 5 hrs by visible light irradiation, compared with pristine ZnS and higher percentage N-doping ZnS photocatalysts.

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