scholarly journals Photocatalytic Degradation of Allura Red by MN-Ni Co-Doped Nanotitania under Visible Light Irradiation

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.

2018 ◽  
Vol 4 (5) ◽  
pp. 555-559
Author(s):  
K.V. Divya Lakshmi ◽  
T. Siva Rao

Nickel and sulfur co-doped TiO2 photocatalyst were prepared by using sol-gel method with dopants precursors of nickel nitrate and thiourea. Prepared samples were characterized by XRD, UV-Vis-DRS, TEM, BET, FT-IR and SEM-EDX. These characterization and experimental results revealed that there is a formation of anatase phase, decreased band gap 2.62 eV for NIST-2, small particle size 7.3 nm and high surface area 142.62 m2/g. The FT-IR frequency shift for Ti-O-Ti was observed from 569 cm-1 to 460-560 cm-1 for co-doped TiO2. The efficiency of photocatalytic and antibacterial was evaluated by degradation of Orange-II dye and Escherichia coli (MTCC-443) respectively. The complete degradation of Orange-II was achieved in 120 min at optimum reaction parameters for NIST-2 at pH-3, catalyst dosage-100 mg/L and initial dye concentration at 10 mg/L.


2021 ◽  
Author(s):  
Ayat Nuri ◽  
Abolfazl Bezaatpour ◽  
Mandana Amiri ◽  
Nemanja Vucetic ◽  
Jyri-Pekka Mikkola ◽  
...  

AbstractMesoporous SBA-15 silicate with a high surface area was prepared by a hydrothermal method, successively modified by organic melamine ligands and then used for deposition of Pd nanoparticles onto it. The synthesized materials were characterized with infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), nitrogen physisorption, scanning electron microscopy (SEM) coupled with energy dispersive X-ray analysis (EDX), transmission electron microscopy (TEM), nuclear magnetic resonance (NMR) and inductively coupled plasma (ICP-OES). The catalyst was effectively used in the Mizoroki–Heck coupling reaction of various reactants in the presence of an organic base giving the desired products in a short reaction time and with small catalysts loadings. The reaction parameters such as the base type, amounts of catalyst, solvents, and the temperature were optimized. The catalyst was easily recovered and reused at least seven times without significant activity losses. Graphic Abstract


2007 ◽  
Vol 43 (3) ◽  
pp. 299-304 ◽  
Author(s):  
Pradeepan Periyat ◽  
K. V. Baiju ◽  
P. Mukundan ◽  
P. Krishna Pillai ◽  
K. G. K. Warrier

Catalysts ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 631 ◽  
Author(s):  
Osmín Avilés-García ◽  
Jaime Espino-Valencia ◽  
Rubí Romero-Romero ◽  
José Rico-Cerda ◽  
Manuel Arroyo-Albiter ◽  
...  

Various W and Mo co-doped titanium dioxide (TiO2) materials were obtained through the EISA (Evaporation-Induced Self-Assembly) method and then tested as photocatalysts in the degradation of 4-chlorophenol. The synthesized materials were characterized by thermogravimetric analysis (TGA), Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD), Raman spectroscopy (RS), N2 physisorption, UV-vis diffuse reflectance spectroscopy (DRS), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). The results showed that the W-Mo-TiO2 catalysts have a high surface area of about 191 m2/g, and the presence of an anatase crystalline phase. The co-doped materials exhibited smaller crystallite sizes than those with one dopant, since the crystallinity is inhibited by the presence of both species. In addition, tungsten and molybdenum dopants are distributed and are incorporated into the anatase structure of TiO2, due to changes in red parameters and lattice expansion. Under our experimental conditions, the co-doped TiO2 catalyst presented 46% more 4-chlorophenol degradation than Degussa P25. The incorporation of two dopant cations in titania improved its photocatalytic performance, which was attributed to a cooperative effect by decreasing the recombination of photogenerated charges, high radiation absorption capacity, high surface areas, and low crystallinity. When TiO2 is co-doped with the same amount of both cations (1 wt.%), the highest degradation and mineralization (97% and 74%, respectively) is achieved. Quinones were the main intermediates in the 4-chlorophenol oxidation by W-Mo-TiO2 and 1,2,4-benzenetriol was incompletely degraded.


2012 ◽  
Vol 626 ◽  
pp. 425-429 ◽  
Author(s):  
N.N. Hafizah ◽  
Mohamed Zahidi Musa ◽  
Mohamad Hafiz Mamat ◽  
M. Rusop

In this study, TiO2nanopowder was synthesized via a sol-gel grinding method. The effects of TiO2precursor concentration of TiO2nanopowder were investigated. The TiO2nanopowder obtained were characterized using X-ray diffraction (XRD), Raman spectroscopy and field emission scanning electron microscopy (FESEM) for their structural properties. From the calculation of the crystallite size in XRD, the size of the nanoparticles obtained is 49.55 nm at the highest TiO2precursor concentration. In contrast, at the lower concentration of 0.4 molar give the cryatallite size of 12.84 nm. Further, XRD and Raman spectrum results confirmed the TiO2nanopowder obtain composed of only anatase phase. The FESEM micrographs of TiO2nanopowder also were discussed in this paper.


2017 ◽  
Vol 2017 ◽  
pp. 1-5 ◽  
Author(s):  
Sana Ahmad ◽  
Anam Nazir ◽  
Tousif Hussain

Titanium dioxide nanoparticles were prepared by a modified sol-gel route. Titanium butoxide was used as precursor and nebulizer was used for a fine spray of particles. The prepared powders were characterized by FT-IR, SEM, XRD, and TGA-DTA methods. The results indicated that nanoparticles with small size and high surface area were synthesized. XRD result indicated that TiO2 nanoparticles were obtained in pure anatase crystalline form with a crystallite size of 40 nm. The catalytic activity of as-synthesized nanoparticles was tested for the degradation of formic acid and toluene.


2022 ◽  
Vol 19 (1) ◽  
pp. 1715
Author(s):  
Imandi Manga Raju ◽  
Tirukkovalluri Siva Rao ◽  
Miditana Sankara Rao

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


2018 ◽  
Vol 56 (1A) ◽  
pp. 219
Author(s):  
Dao Viet Thang

In this study, multiferroicMultiferroic Bi1-xYxFe0.975Ni0.025O3 (x = 0.00, 0.05, 0.10, and 0.15) called as (Y, Ni)                co-doped BiFeO3 materials were synthesized by a sol-gel method.  and characterized by X-ray diffraction diagrams and(XRD), energy-dispersive X-ray (EDX) and vibrating sample magnetization (VSM) measurements demonstrated. The result showed that Bi1-xYxFe0.975Ni0.025O3all investigated materials waspresent a single phase of the perovskite-type rhombohedral structure. Ferromagnetism and ferroelectricity of the Bi1-xYxFe0.975Ni0.025O3 materials have been investigated. Results showed that the co-doping by (Y, Ni) for (Bi, Fe)  have affected in enhancing by the (Y, Ni) co-doping, as a result the ferroelectric polarization and magnetization of BiFeO3. The magnetic characterization indicated that the ferromagnetic behavior wasthe initial BiFeO3 materialwere enhanced with increasing concentration of Y3+ for (Y, Ni) co-substituted of BiFeO3. Which could beion. It is attributed to the defferentdifference of the magnetic momentmoments of Ni2+ and Fe3+, and+ ions, as well as the Y3+-Fe3+,+ and Y3+-Ni2+ super-exchange interaction. Theinteractions. The characteristics of the investigated materials, such as remanent magnetization (Mr), saturation magnetization (Ms), remanent polarization (2Pr) and saturation polarization (2Ps) continuously increase upon increasing in the range of x from 0.00 to 0.15. When x = 0.15, the values of Mr and Ms are 0.078 and 0.794 emu/g, respectively. The values of 2Pr and 2Ps are 16.58 and 27.99 µC/cm2, respectively. Origin of ferromagnetic and ferroelectric properties of Bi1-xYxFe0.975Ni0.025O3 materials will be discussed in this paper.


2016 ◽  
Vol 720 ◽  
pp. 252-256
Author(s):  
Nadia Mohammed Elmassalami Ayad ◽  
Andre Ben Hur da Silva Figueiredo ◽  
Wilma de Araujo Gonzalez ◽  
Daniel Navarro da Rocha ◽  
Rubens Lincoln Santana Blazutti Marçal ◽  
...  

Bioactive glasses have widely used in biomedical applications such as bone filler due to their excellent biocompatibility, bioactivity and osteoconduction characteristics. In this work, a silicate-rich glass was synthesized by the sol-gel method with 60% SiO2 – 30%CaO – 10% MgO composition where fumed silica acts as the silica precursor. This new method was hypothesized to reduce the gel formation time, due to the high surface area of the fumed silica. In addition, this would presumably increase the nanoporosity of the glass. For comparison purposes, we used a glass of the same composition, but with the conventional silica precursor, tetraethyl orthosilicate (TEOS), through the sol gel method. Both were heat treated at 450°C. FT-IR analysis before and after heat treatment at 450°C showed the presence of nitrate groups, especially in the TEOS samples. This is consistent with the more hygroscopic aspect of those samples. The fumed silica samples had significantly less pronounced peaks corresponding to the nitrate groups, consistent with the more porous structure and the less hygroscopic aspect. The fumed silica samples indeed had a lower gelling time and showed similar results obtained by XRD and FT-IR analyses, showing that the use of fumed silica is viable and advantageous in the glass synthesis by the sol-gel process


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