Photocatalytic Activity of W Doped Ta2O5 Particles for Methylene Blue Degradation under UV-Light

2011 ◽  
Vol 197-198 ◽  
pp. 281-284 ◽  
Author(s):  
Yan Hong Zhao ◽  
Li Chun Hou ◽  
Xiang Li ◽  
Xiaodong Yang ◽  
Xiao Jing Wang
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Uv Light ◽  
Tantalum Oxide ◽  
X Ray Diffraction ◽  
Orthorhombic Crystal ◽  
Methylene Blue Degradation ◽  
X Ray ◽  
First Order ◽  
Kinetics Of

Tungsten doped tantalum oxide (W-Ta2O5) particles were synthesized by a low temperature hydrothermal method. The phase structure of W-Ta2O5particles was characterized by X-ray diffraction (XRD). The XRD results indicated that the samples belonged to orthorhombic crystal. The photocatalytic activity of samples was investigated with degradation methylene blue (MB) under ultraviolet light. The degradation efficiency of MB under the catalysis of W-Ta2O5particles attained 91% when the reaction time was 7 h. The kinetics of MB degradation was respect to the first-order in the presence of the photocatalysts.

Catalytic Activity of Ba Doped Ta2O5 for Methylene Blue Degradation under Visible Light

2010 ◽  
Vol 156-157 ◽  
pp. 1440-1443
Author(s):  
Yan Hong Zhao ◽  
Min Sun ◽  
Shu Wei Wang ◽  
Wen Ming Tong ◽  
Xiao Jing Wang
Keyword(s):  
Methylene Blue ◽  
Catalytic Activity ◽  
Visible Light ◽  
Tantalum Oxide ◽  
X Ray Diffraction ◽  
Methylene Blue Degradation ◽  
X Ray ◽  
First Order ◽  
Good Crystallinity ◽  
Kinetics Of

The Ba doped tantalum oxide (Ba-Ta2O5) particles were synthesized using low temperature hydrothermal method. The phase structure of samples was characterized by X-ray diffraction (XRD). The result showed that Ba-Ta2O5 had still good crystallinity and belonged to rhombic crystal. The catalytic activity of samples was investigated with the degradation methylene blue (MB) under visible light. The degradation efficiency attained 82% when the reaction time was 12 h. The kinetics of MB degradation was respect to the first-order.

Electrochemical Property of Terbium Doped Tantalum Oxide Film Electrode

2011 ◽  
Vol 301-303 ◽  
pp. 16-21 ◽  
Author(s):  
Yan Hong Zhao ◽  
Li Chun Hou ◽  
Wen Fei Liu ◽  
Sheng Liang ◽  
Xiao Jing Wang
Keyword(s):  
Electrochemical Property ◽  
Tantalum Oxide ◽  
Electrochemical Kinetics ◽  
Film Electrode ◽  
X Ray Diffraction ◽  
Orthorhombic Crystal ◽  
X Ray ◽  
Potential Applications ◽  
Kinetics Of ◽  
Tantalum Oxide Film

Terbium doped tantalum oxide (Tb-Ta2O5) particles were synthesized with a low hydrothermal method. The phase structure of Tb-Ta2O5 obtained was performed by X-ray diffraction (XRD). The result revealed that the terbium doped Ta2O5 belongs to orthorhombic crystal. The electrochemical property of methylene blue (MB) at Tb-Ta2O5 film electrode in 0.5 mol dm-3 KCl aqueous solution was investigated with cyclic voltgrammetry (CV). The CV result indicated that the electrochemical kinetics of MB was diffusion controlling at Tb-Ta2O5 film electrode. Tb dopping imporved the electrochemical property of Ta2O5 film electrode. Tb-Ta2O5 is used as a kind of electrode material which has some new potential applications.

scholarly journals Synthesis of copper oxide nano-rice structures for enhancement of photocatalytic activity under natural sunlight

2019 ◽  
Vol 20 (5) ◽  
pp. 253-262
Author(s):  
Roonak Abdul Salam A.Alkareem
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Electron Microscope ◽  
Copper Oxide ◽  
High Photocatalytic Activity ◽  
X Ray Diffraction ◽  
Methylene Blue Degradation ◽  
X Ray ◽  
Uv Visible ◽  
Scanning Electron

In this work, copper oxide (CuO) nano-rice structure was prepared by hydrothermal method. The prepared samples were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FESEM), and UV-visible spectrophotometer. CuO nano-rice structure showed high photocatalytic activity towards degradation of methylene blue (MB). Hydrothermally growth of CuO provided uniformly distributed nano-rice structures with high degradation efficiency (90.41%) and rate constant (kt) 16.6 × 10-2 min-1 for methylene blue degradation.

The Influence of ZnO Components on the Photocatalytic Activity of Fe3O4-CuO-ZnO Nanocomposites

2015 ◽  
Vol 1123 ◽  
pp. 227-232 ◽  
Author(s):  
Iqriah Kalim Susanto ◽  
Ardiansyah Taufik ◽  
Rosari Saleh
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Diffuse Reflectance Spectroscopy ◽  
Uv Light ◽  
Sol Gel ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Uv Visible

Nanocomposite Fe3O4-CuO-ZnO with different molar ratio of Fe3O4:CuO:ZnO were synthesized using sol-gel method and characterized by X-ray diffraction, energy dispersive X-ray spectroscopy, field emission scanning electron microscope, UV-visible diffuse reflectance spectroscopy and vibrating sample magnetometer. The characterization results manifested that the combination of Fe3O4, CuO and ZnO nanoparticles was successful. The photocatalytic activity of nanocomposite with the molar ratio of 1:1:5 was more effective in the degradation of methylene blue under UV light irradiation than pure Fe3O4, CuO, ZnO. The role of photoactive species involved in the photocatalytic reaction was studied and found that holes play the most important role in photodegradation of methylene blue.

Efficient adsorption of chlorpyrifos onto modified activated carbon by gamma irradiation; a plausible adsorption mechanism

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Mohamed S. Yahia ◽  
Ahmed S. Elzaref ◽  
Magdy B. Awad ◽  
Ahmed M. Tony ◽  
Ahmed S. Elfeky
Keyword(s):  
Gamma Irradiation ◽  
Area Measurement ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
First Order ◽  
Pseudo Second Order ◽  
Ft Ir ◽  
Pseudo First Order ◽  
Kinetics Of

Abstract Commercial Granulated Active Carbon (GAC) has been modified using 10 Gy dose Gamma irradiation (GAC10 Gy) for increasing its ability of air purification. Both, the raw and treated samples were applied for removing Chlorpyrifos pesticide (CPF) from ambient midair. Physicochemical properties of the two materials were characterized by Fourier Transform Infrared (FT-IR) and Raman spectroscopy. The phase formation and microstructure were monitored using X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), supported with Energy-Dispersive X-ray (EDX). The Surface area measurement was detected using BET particle size prosometry. Obtained outcomes showed that, the maximum adsorption capacity, given by Langmuir equations, was greatly increased from 172.712 to 272.480 mg/g for GAC and GAC10 Gy, respectively, with high selectivity. The overall removal efficiency of GAC10 Gy was notably comparable to that of the original GAC-sorbent. The present study indicated that, gamma irradiation could be a promising technique for treating GAC and turned it more active in eliminating the pesticides pollutants from surrounding air. The data of equilibrium has been analyzed by Langmuir and Freundlich models, that were considerably better suited for the investigated materials than other models. The process kinetics of CPF adsorbed onto both tested carbon versions were found to obey the pseudo first order at all concentrations with an exception at 70 mg/l using GAC, where, the spontaneous exothermic adsorption of Chlorpyrifos is a strong function for the pseudo-first order (PFO) and pseudo second order (PSO) kinetics.

Photocatalytic Activity of Fe-Doped ZnO/Montmorillonite Nanocomposite for Degradation of Malachite Green

2015 ◽  
Vol 827 ◽  
pp. 19-24 ◽  
Author(s):  
Nur Afifah ◽  
Nadia Febiana Djaja ◽  
Rosari Saleh
Keyword(s):  
Photocatalytic Activity ◽  
Malachite Green ◽  
Organic Dyes ◽  
Uv Light ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Spin Resonance ◽  
Doped Zno ◽  
Co Precipitation

In this study, the photocatalytic activity of pure Fe- doped ZnO and Fe- doped ZnO/Montmorillonite nanocomposite has been investigated for the degradation of malachite green under UV light irradiation. Both photocatalysts were synthesized using co-precipitation method and characterized by X-ray diffraction, energy dispersive X-ray spectroscopy, Fourier-transform infrared absorption, and electron spin resonance. The results showed that the photocatalytic efficiency is better in the presence of montmorillonite compared to pure Fe- doped ZnO. To detect the possible reactive species involved in degradation of organic dyes control experiments with introducing scavengers into the solution of organic dyes were carried out. It is found that electron plays an important role in the degradation of malachite green.

Oxidation of Nickel(II) and Manganese(II) by Peroxodisulfate in Aqueous Solution in the Presence of Molybdate. Crystal Structure of the (NH4)6[NiMo9O32].6H2O Product

1992 ◽  
Vol 45 (12) ◽  
pp. 1943 ◽  
Author(s):  
SJ Dunne ◽  
RC Burns ◽  
GA Lawrance
Keyword(s):  
Rate Constant ◽  
Linear Dependence ◽  
Ph Dependence ◽  
Order Rate Constant ◽  
X Ray Diffraction ◽  
X Ray ◽  
First Order ◽  
Oxidant Concentration ◽  
Ph Range ◽  
Kinetics Of

Oxidation of Ni2+,aq, by S2O82- to nickel(IV) in the presence of molybdate ion, as in the analogous manganese system, involves the formation of the soluble heteropolymolybdate anion [MMogO32]2- (M = Ni, Mn ). The nickel(IV) product crystallized as (NH4)6 [NiMogO32].6H2O from the reaction mixture in the rhombohedra1 space group R3, a 15.922(1), c 12.406(1) � ; the structure was determined by X-ray diffraction methods, and refined to a residual of 0.025 for 1741 independent 'observed' reflections. The kinetics of the oxidation were examined at 80 C over the pH range 3.0-5.2; a linear dependence on [S2O82-] and a non-linear dependence on l/[H+] were observed. The influence of variation of the Ni/Mo ratio between 1:10 and 1:25 on the observed rate constant was very small at pH 4.5, a result supporting the view that the precursor exists as the known [NiMo6O24H6]4- or a close analogue in solution. The pH dependence of the observed rate constant at a fixed oxidant concentration (0.025 mol dm-3) fits dequately to the expression kobs = kH [H+]/(Ka+[H+]) where kH = 0.0013 dm3 mol-1 s-1 and Ka = 4-0x10-5. The first-order dependence on peroxodisulfate subsequently yields a second-order rate constant of 0.042 dm3 mol-1 s-1. Under analogous conditions, oxidation of manganese(II) occurs eightfold more slowly than oxidation of nickel(II), whereas oxidation of manganese(II) by peroxomonosulfuric acid is 16-fold faster than oxidation by peroxodisulfate under similar conditions.

scholarly journals Copper oxide supported on graphene for phodegradation of rhodamine B

2015 ◽  
Vol 11 (4) ◽  
Author(s):  
Nurul Sahida Hassan ◽  
Nurul Jamilah Roslani ◽  
Aishah Abdul Jalil ◽  
Sugeng Triwahyono ◽  
Nur Fatien Salleh ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Copper Oxide ◽  
Photocatalytic Degradation ◽  
Rhodamine B ◽  
Industrial Wastewater ◽  
Water Contamination ◽  
X Ray Diffraction ◽  
Composite Photocatalyst ◽  
X Ray ◽  
First Order

In recent years, dyes are one of the major sources of the water contamination that lead to environmental problems. For instance, Rhodamine B (RhB) which was extensively used as a colorant in textile industries is toxic and carcinogenic. Among many techniques, photocatalytic degradation become the promising one to remove those dyes from industrial wastewater. Recently, graphene has shown outstanding performance in this application due to its intrinsic electron delocalisation which promotes electron transport between composite photocatalyst and pollutant molecules. While, copper oxide (CuO) is well-known has a lower bandgap energies compared to other semiconductors. Therefore, in this study, copper oxide supported on graphene (CuO/G) was prepared and its photocatalytic activity was tested on degradation of RhB. The catalysts were characterized by X-Ray Diffraction (XRD) and Fourier Transform Infrared (FTIR) Spectroscopy. The results showed that the interaction between copper and graphene support could enhance the photocatalytic activity. The 5 wt% CuO/G was found to give the highest degradation (95%) of 10 mg L-1 of RhB solution at pH 7 using 1 g L-1 catalyst after 4 hours under visible light irradiation. The photodegradation followed the pseudo first-order Langmuir-Hinshelwood kinetic model. This study demonstrated that the CuO/G has a potential to be used in photocatalytic degradation of various organic pollutants.

scholarly journals Influence of Cu(NO3)2 content used in thermal shock method on the photocatalytic activity of Cu-Modified ZnO nanoparticles

2021 ◽  
Vol 5 (3) ◽  
pp. first
Author(s):  
Thế Luân Nguyễn ◽  
Tiến Khoa Lê ◽  
Châu Ngọc Hoàng ◽  
Hữu Khánh Hưng Nguyễn ◽  
Thị Kiều Xuân Huỳnh
Keyword(s):  
Crystal Structure ◽  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Thermal Shock ◽  
Photoelectron Spectroscopy ◽  
Copper Content ◽  
Uv Light ◽  
Copper Nitrate ◽  
X Ray ◽  
Doped Zno

The Cu doped ZnO photocatalysts were prepared on ZnO substrate modified with copper nitrate by thermal shock method with different ratio % molar Cu : Zn = 0.3, 0.5, 1.0, 2.0 and 5.0 in order to study the impacts of copper content on the photocatalytic activity of ZnO under both UV and Vis light irradiation. The crystal structure, morphology bulk and surface were investigated by X-ray diffraction (XRD), transmission electron microscopy (TEM), fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). Their photocatalytic activities were studied via time-dependent degradation of methylene blue in aqueous solution. The results exhibit that crystal structure and morphology of Cu doped ZnO photocatalysts is not modified significally than ZnO original but surface charateristicschanged greatly. The photocatalyst was doped with copper content under 2% showed formation of Cu species. These samples perform photocatalytic activity higher than ZnO. The CuNZO-0.05-500 had the highest rate constants for methylene blue degradation (kUV = 6,901 h-1, kVIS = 0,224 h-1), which are about 2.2 times and 1.3 times higher than unmodified ZnO under UV light and Vis light, respectively. However, the CuNZO-5.0-500 which had the formation of CuO phase and unchangeable ZnO's surface has photocatalytic activity similar to pure ZnO.

scholarly journals Photocatalytic Activity and Optical Properties of Blue Persistent Phosphors under UV and Solar Irradiation

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
C. R. García ◽  
L. A. Diaz-Torres ◽  
J. Oliva ◽  
M. T. Romero ◽  
P. Salas
Keyword(s):  
Photocatalytic Activity ◽  
Annealing Temperature ◽  
Uv Light ◽  
Solar Irradiation ◽  
Photoluminescence Spectra ◽  
X Ray Diffraction ◽  
X Ray ◽  
Water Cleaning ◽  
Different Temperatures ◽  
The Eu

Blue phosphorescent strontium aluminosilicate powders were prepared by combustion synthesis route and a postannealing treatments at different temperatures. X-ray diffraction analysis showed that phosphors are composed of two main hexagonal phases: SrAl2O4and Sr3Al32O51. The morphology of the phosphors changed from micrograins (1000°C) to a mixture of bars and hexagons (1200°C) and finally to only hexagons (1300°C) as the annealing temperature is increased. Photoluminescence spectra showed a strong blue-green phosphorescent emission centered atλem=455 nm, which is associated with4f65d1→4f6  (8S7/2)transition of the Eu2+. The sample annealed at 1200°C presents the highest luminance value (40 Cd/m2) with CIE coordinates (0.1589, 0.1972). Also, the photocatalytic degradation of methylene blue (MB) under UV light (at 365 nm) was monitored. Samples annealed at 1000°C and 1300°C presented the highest percentage of degradation (32% and 38.5%, resp.) after 360 min. In the case of photocatalytic activity under solar irradiation, the samples annealed at 1000°C, 1150°C, and 1200°C produced total degradation of MB after only 300 min. Hence, the results obtained with solar photocatalysis suggest that our powders could be useful for water cleaning in water treatment plants.

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