scholarly journals An Efficient Photocatalytic Degradation of Methyl Blue Dye by using Synthesised PbO Nanoparticles

2012 ◽  
Vol 9 (2) ◽  
pp. 705-715 ◽  
Author(s):  
Ashok V. Borhade ◽  
Dipak R. Tope ◽  
Bhagwat K. Uphade

We report here the synthesis of visible light sensitive PbO and Ni doped PbO nanoparticles by hydrothermal method and characterized by UV-DRS, photoluminescence spectroscopy (PL), FTIR, X-ray diffraction (XRD), SEM, EDAX and TGA. Further an efficient approach has been developed for degradation of methyl blue (MB) in aqueous medium. The photodegradation of dye was monitored as a function of dye concentration, pH and catalyst amount has been determined. The reduction in the chemical oxygen demand (COD) revealed the mineralization of dye along with colour removal.

2015 ◽  
Vol 72 (12) ◽  
pp. 2122-2131 ◽  
Author(s):  
MengMeng Xu ◽  
YaLei Zhao ◽  
QiShe Yan

Bi7O9I3, a kind of visible-light-responsive photocatalyst, with hierarchical micro/nano-architecture was successfully synthesized by oil-bath heating method, with ethylene glycol as solvent, and applied to degrade sulfonamide antibiotics. The as-prepared product was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV-visible diffuse reflection spectra and scanning electron microscopy (SEM). XRD and XPS tests confirmed that the product was indeed Bi7O9I3. The result of SEM observation shows that the as-synthesized Bi7O9I3 consists of a large number of micro-sheets with parallel rectangle structure. The optical test exhibited strong photoabsorption in visible light irradiation, with 617 nm of absorption edges. Moreover, the difference in the photocatalytic efficiency of as-prepared Bi7O9I3 at different seasons of a whole year was investigated in this study. The chemical oxygen demand removal efficiency and concentration of NO3− and SO42– of solution after reaction were also researched to confirm whether degradation of the pollutant was complete; the results indicated a high mineralization capacity of Bi7O9I3. The as-synthesized Bi7O9I3 exhibits an excellent oxidizing capacity of sulfadiazine sodium and favorable stability during the photocatalytic reaction.


2020 ◽  
Author(s):  
Chukwunonso Onyenanu ◽  
Lovet Emembolu

Abstract Photocatalytic activity of the natural semiconducting sphalerite mineral from Abuni, Nasarawa State, Nigeria was studied for the degradation of methylene blue (MB). Natural Sphalerite as a visible – light responsive photocatalyst was characterized by X ray diffraction (XRD), X ray fluorescence (XRF) and surface area analysis. To further enhance the photocatalytic activity of natural Sphalerite, the chemical composition of the sphalerite was varied via leaching with oxalic acids. The photocatalytic activity of the Natural sphalerite, leached sphalerite and as well as the calcined leachates was tested for MB degradation under visible light illumination. The result shows a very high percentage of MB degradation by natural sphalerite after 60mintues of light irradiation time. A composite of ZnO -α –Fe2O3 -ϒ-Fe2O3 with traces amount of MoO and MnO2 was synthesized by calcination of the obtained leachates at 1000°C for 4hours. The photocatalytic degradation of methylene blue dye follows pseudo first order kinetics.


Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 332
Author(s):  
Evangelia Vasilaki ◽  
Nikos Katsarakis ◽  
Spyros Dokianakis ◽  
Maria Vamvakaki

Core-shell heterostructures with a complex, flower-like morphology, comprising a ZnO core and a TiO2 shell decorated with reduced graphene oxide (rGO) sheets by hydrothermal wrapping, are reported to extend the absorption properties of the semiconductors toward the visible light range. The ternary photocatalysts were characterized by X-ray diffraction, field emission scanning electron microscopy, Raman spectroscopy, diffuse reflectance UV–Vis, and attenuated total reflectance-Fourier transform infrared spectroscopy. Its photocatalytic performance was evaluated under visible light irradiation using methylene blue dye as a model pollutant. The rGO-modified ZnO–TiO2 photocatalyst exhibited superior photoactivity compared to that of the parent ZnO–TiO2 core-shell structures, which was dependent on its graphene content. The enhanced photocatalytic response was attributed to the higher absorption in the visible light range, as well as the pronounced electron and hole separation in the ternary system.


2018 ◽  
Vol 55 (4C) ◽  
pp. 277 ◽  
Author(s):  
Nguyen Thi Phuong Mai

In the present paper, photocatalytic degradation of paraquat using N-TiO2/SiO2 with different molar ratio of titanium: nitrogen (Ti:N) under visible light was investigated. The catalyst was prepared via immersed SiO2 in N-TiO2. N-TiO2 was synthesized by sol-gel method.  The N-TiO2/SiO2 catalyst was characterized using X-ray diffraction, UV diffuse reflectance spectroscopy, scanning electron microscopy, energy dispersive X-ray spectroscopy. The results from characterizations indicated that N-doped anatase TiO2 had a 20-25 nm size. Degradation of paraquat, at an initial concentration of 10 mg/L was determined by UV-Vis. Chemical oxygen demand (COD) was used for process performance. Based on the COD tests, the COD values in residual paraquat was lower than that in initial paraquat concentration after 8 hours illumination of visible light. Moreover, the experiment’s results indicated that 80% of paraquat was degraded within 8 h of illumination time. These results showed that N-TiO2/SiO2 with molar Ti:N=2:1 gives the highest degradation efficiency of paraquat under visible light. This catalyst was stable and reusable suggesting it can be applied to treat organic pollutant in water. 


2020 ◽  
Vol 20 (9) ◽  
pp. 5759-5764
Author(s):  
V. Karthikeyan ◽  
G. Gnanamoorthy ◽  
P. Varun Prasath ◽  
V. Narayanan ◽  
Suresh Sagadevan ◽  
...  

Herein, we report the facile synthesis, characterization and visible-light-driven photocatalytic degradation of perforated curly Zn0.1Ni0.9O nanosheets synthesized by hydrothermal process. The X-ray diffraction (XRD) and scanning electron microscopy (SEM) studies confirmed the cubic phase crystalline structure and growth of high density perforated curly Zn0.1Ni0.9O nanosheets, respectively. As a photocatalyst, using methylene blue (MB) as model pollutant, the synthesized nanosheets demonstrated a high degradation efficiency of ~76% in 60 min under visible light irradiation. The observed results suggest that the synthesized Zn0.1Ni0.9O nanosheets are attractive photocatalysts for the degradation of toxic organic waste in the water under visible light.


2021 ◽  
pp. 096739112110601
Author(s):  
Mojgan Zendehdel ◽  
Faezeh Hossein Nouri

Ag-Clinoptilolite/Polyethersulfone (PES/Clin/AgNPs) nanofiber was synthesized through the electrospinning method. The effect of solvent, the amount of Ag-Clinoptilolite, and PES were investigated. Parameters such as electric field, spinning distance, and concentration of the dope solution were studied in order to demonstrate their effects on the electrospinning ability and morphology of the nanofiber. The structure of PES/Clin/AgNPs nanofiber was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy-dispersive X-ray spectroscopy (EDX) analyses. In the optimum conditions, the nanofibers could be prepared at the size of 250–800 nm. Then, their ability to remove chemical oxygen demand (COD) from real wastewater was studied. The result revealed about 85% removal of COD at pH = 10 and in 10 min for PES/Clin/AgNPs (25%). A successful fabrication method using low-cost natural zeolite and the green polymer was introduced. The reusability of the column was assessed.


Catalysts ◽  
2021 ◽  
Vol 11 (8) ◽  
pp. 899
Author(s):  
Murendeni P. Ravele ◽  
Opeyemi A. Oyewo ◽  
Damian C. Onwudiwe

Pure-phase Cu2−xS (x = 1, 0.2) nanoparticles have been synthesized by the thermal decomposition of copper(II) dithiocarbamate as a single-source precursor in oleylamine as a capping agent. The compositions of the Cu2−xS nanocrystals varied from CuS (covellite) through the mixture of phases (CuS and Cu7.2S4) to Cu9S5 (digenite) by simply varying the temperature of synthesis. The crystallinity and morphology of the copper sulfides were studied using X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM), which showed pure phases at low (120 °C) and high (220 °C) temperatures and a mixture of phases at intermediate temperatures (150 and 180 °C). Covellite was of a spherical morphology, while digenite was rod shaped. The optical properties of these nanocrystals were characterized by UV−vis–NIR and photoluminescence spectroscopies. Both samples had very similar absorption spectra but distinguishable fluorescence properties and exhibited a blue shift in their band gap energies compared to bulk Cu2−xS. The pure phases were used as catalysts for the photocatalytic degradation of tetracycline (TC) under visible-light irradiation. The results demonstrated that the photocatalytic activity of the digenite phase exhibited higher catalytic degradation of 98.5% compared to the covellite phase, which showed 88% degradation within the 120 min reaction time using 80 mg of the catalysts. The higher degradation efficiency achieved with the digenite phase was attributed to its higher absorption of the visible light compared to covellite.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jeasmin Akter ◽  
Md. Abu Hanif ◽  
Md. Akherul Islam ◽  
Kamal Prasad Sapkota ◽  
Jae Ryang Hahn

AbstractA convenient route was developed for the selective preparation of two stable nanocomposites, Ti3+/TiO2/CNT (labeled as TTOC-1 and TTOC-3) and Ti3+/TiO2/carbon layer (labeled as TTOC-2), from the same precursor by varying the amount of single-walled carbon nanotubes used in the synthesis. TiO2 is an effective photocatalyst; however, its wide bandgap limits its usefulness to the UV region. As a solution to this problem, our prepared nanocomposites exhibit a small bandgap and wide visible-light (VL) absorption because of the introduction of carbonaceous species and Ti3+ vacancies. The photocatalytic efficiency of the nanocomposites was examined via the degradation of methylene blue dye under VL. Excellent photocatalytic activity of 83%, 98%, and 93% was observed for TTOC-1, TTOC-2, and TTOC-3 nanocomposites within 25 min. In addition, the photocatalytic degradation efficiency of TTOC-2 toward methyl orange, phenol, rhodamine B, and congo red was 28%, 69%, 71%, and 91%, respectively, under similar experimental conditions after 25 min. Higher reusability and structural integrity of the as-synthesized photocatalyst were confirmed within five consecutive runs by photocatalytic test and X-ray diffraction analysis, respectively. The resulting nanocomposites provide new insights into the development of VL-active and stable photocatalysts with high efficiencies.


2011 ◽  
Vol 383-390 ◽  
pp. 3188-3191
Author(s):  
Han Jie Huang ◽  
Wen Long She ◽  
Ling Wen Yang ◽  
Hai Peng Huang

A visible-light-responsive TiO2-xNx photocatalyst was prepared by a very simple method. Ammonia solution was used as nitrogen resource in this paper. The TiO2-xNx photocatalyst was characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET), UV-Vis diffuse reflection spectra (DRS), and X-ray photoelectron spectroscopy (XPS). The ethylene was selected as a target pollutant under visible light excitation to evaluate the activity of this photocatalyst. The new prepared TiO2-xNx photocatalyst with strong photocatalytic activity under visible light irradiation was demonstrated in the experiment.


2016 ◽  
Vol 703 ◽  
pp. 316-320
Author(s):  
Hai Feng Chen ◽  
Jing Ling Hu ◽  
Bing Xu

Using NH4VO3, Bi (NO3)3•5H2O and Co (NO3)2•6H2O as raw materials, Co doped BiVO4 (Co/BiVO4) photocatalysts were successfully prepared by solid state method. And the photo catalytic properties were test in this work. Crystal structures of these samples were characterized by X-ray diffraction (XRD). The Methyl Orange (MO) was simulated as the sewage under the visible light to explorer the influence of the illumination time and the mass of photocatalyst. The visible-light absorption spectrum of BiVO4 was broadening with doping Co. It was found that the Co/BiVO4 had higher photocatalytic activity than pure BiVO4 .The reason of enhanced catalytic effect also had been analyzed and discussed in the article.


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