scholarly journals Preparation of Multicycle GO/TiO2 Composite Photocatalyst and Study on Degradation of Methylene Blue Synthetic Wastewater

2019 ◽  
Vol 9 (16) ◽  
pp. 3282 ◽  
Author(s):  
Zhongtian Fu ◽  
Song Zhang ◽  
Zhongxue Fu
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Raw Materials ◽  
Anatase Phase ◽  
Pure Tio2 ◽  
Synthetic Wastewater ◽  
X Ray Diffraction ◽  
Experimental Conditions ◽  
Composite Photocatalyst ◽  
Initial Ph

A series of composite photocatalysts were prepared by using graphene oxide (GO) prepared by modified Hummers method and TiO2 hydrogel prepared by using butyl titanate as raw materials. The composite photocatalyst was characterized through scanning electron microscope（SEM）, x ray diffraction （XRD）, and Raman spectroscopy, and the degradation effect of pure TiO2 and composite photocatalyst on methylene blue (MB) dye wastewater under different experimental conditions was studied. The results showed that TiO2 in composite photocatalyst was mainly anatase phase and its photocatalytic activity was better than pure TiO2. When the addition of GO reached 15 wt%, the photocatalytic activity was the highest. When 200 mg composite photocatalyst was added to 200 mL synthetic wastewater with a concentration of 10 mg/L and an initial pH of about 8, the degradation rate could reach 95.8% after 2.5 h. It is presumed that the photogenerated charges of GO/TiO2 composite photocatalyst may directly destroy the luminescent groups in the MB molecule and thus decolorize the wastewater, and no other new luminescent groups are generated during the treatment.

scholarly journals Co/TiO2 nanoparticles: preparation, characterization and its application for photocatalytic degradation of methylene blue

2018 ◽  
Author(s):  
azadeh ebrahimian pirbazari ◽  
Pejman Monazzam ◽  
Behnam Fakhari Kisomi
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Tio2 Nanoparticles ◽  
Anatase Phase ◽  
Sol Gel ◽  
Pure Tio2 ◽  
Cobalt Doping ◽  
X Ray Diffraction ◽  
X Ray ◽  
Ft Ir

In this work, TiO2 nanoparticles containing different amounts of cobalt were synthesized by sol-gel method using titanium (IV) isopropoxide and cobalt chloride as titanium and cobalt precursors, respectively. X-ray diffraction (XRD) results showed prepared samples include 100% anatase phase. The presence of cobalt in TiO2 nanoparticle network was established by XRD, scanning electron microscopy equipped with energy dispersive X-ray microanalysis (SEM-EDX), Fourier transform infrared (FT-IR) and N2 physisorption techniques. The increase of cobalt doping enhanced redshif in the diffuse reflectance spectra. The photocatalytic activity of the prepared samples was tested for degradation of methylene blue (MB) as a model of dye. Although the photocatalytic activity of pure TiO2 was found to be higher than that of Co/TiO2 samples under UV irradiation, the presence of 0.24% cobalt dopant in TiO2 nanoparticles resulted in a photocatalyst with the highest activity under visible light

Preparation and Photocatalytic Activity of TiO2/Tourmaline Composite Catalyst

2013 ◽  
Vol 800 ◽  
pp. 464-470 ◽  
Author(s):  
Wei Chao Liu ◽  
Huan Yan Xu ◽  
Tian Nuo Shi ◽  
Li Cheng Wu ◽  
Ping Li
Keyword(s):  
Photocatalytic Activity ◽  
Sintering Temperature ◽  
Anatase Phase ◽  
Sol Gel ◽  
Rutile Phase ◽  
Composite Catalyst ◽  
Nanosized Particles ◽  
X Ray Diffraction ◽  
Composite Photocatalyst ◽  
X Ray

TiO2/tourmaline composite photocatalyst was prepared by sol-gel method using tetrabutyl orthotitanate (Ti (OC4H9)4) as a precursor. As a comparison, pure TiO2 was prepared at the same experimental conditons without the addition of tourmaline. The obtained composite photocatalyst was characterized by X-Ray diffraction (XRD) and scanning electron microscope (SEM) and its photocatalytic activity was also investigated through the photodiscoloration of methyl orange (MO) under UV irradiation. The XRD results indicated that, in the composite photocatalyst, TiO2 existed in the form of anatase and rutile, with the sintering temperature and tourmaline content increasing, the anatase phase trended to the transformation to rutile phase. The SEM results revealed that the nanosized particles of TiO2 were well dispersed and immobilized on the surface of tourmaline, especially for the sample with 2% tourmaline content. Compared with pure TiO2, the composite photocatalyst exhibited a higher photocatalytic activity. When the pure TiO2 was used as the photocatalyst, the MO discoloration ratio only reached 55%. However, the MO discoloration ratio could approach 100% in presence of TiO2/tourmaline composit photocatalyst under the same conditions. The effects of tourmaline content and sintering temperature on the photocatalytic activity of the composite were studied in this work and the results suggested that the sample with 2% tourmaline content and sintered at the temperature of 550°C exhibited the best photocatalytic activity. Finally, the possible mechanism for the photodiscoloration of MO was put forward.

Enhanced photocatalytic activity of CeO2 using β-cyclodextrin on visible light assisted decoloration of methylene blue

2013 ◽  
Vol 69 (1) ◽  
pp. 113-119 ◽  
Author(s):  
Sakthivel Pitchaimuthu ◽  
Ponnusamy Velusamy
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Inclusion Complexation ◽  
Processing Parameters ◽  
Operational Parameters ◽  
Illumination Time ◽  
Operational Conditions ◽  
Electron Microscopy Analysis ◽  
Initial Ph

An attempt has been made to enhance the photocatalytic activity of CeO2 for visible light assisted decoloration of methylene blue (MB) dye in aqueous solutions by β-cyclodextrin (β-CD). The inclusion complexation patterns between host and guest (i.e., β-CD and MB) have been confirmed with UV–visible spectral data. The interaction between CeO2 and β-CD has also been characterized by field emission scanning electron microscopy analysis. The photocatalytic activity of the catalyst under visible light was investigated by measuring the photodegradation of MB in aqueous solution. The effects of key operational parameters such as initial dye concentration, initial pH, CeO2 concentration as well as illumination time on the decolorization extents were investigated. Among the processing parameters, the pH of the reaction solution played an important role in tuning the photocatalytic activity of CeO2. The maximum photodecoloration rate was achieved at basic pH (pH 11). Under the optimum operational conditions, approximately 99.6% dye removal was achieved within 120 min. The observed results indicate that the decolorization of the MB followed a pseudo-first order kinetics.

scholarly journals The Removal of Methylene Blue Dye from Aqueous Solutions Using Activated and Non-Activated Bentonites

2003 ◽  
Vol 21 (5) ◽  
pp. 451-462 ◽  
Author(s):  
Sameer Al-Asheh ◽  
Fawzi Banat ◽  
Leena Abu-Aitah
Keyword(s):  
Methylene Blue ◽  
Ph Value ◽  
Sodium Dodecyl ◽  
Freundlich Isotherm ◽  
Blue Dye ◽  
Batch Adsorption ◽  
Ionic Surfactant ◽  
Methylene Blue Dye ◽  
X Ray Diffraction ◽  
Initial Ph

An improvement in the adsorption capacity of naturally available bentonite towards water pollutants such as Methylene Blue dye (MBD) is certainly needed. For this purpose, sodium bentonite was activated by two methods: (1) treatment with sodium dodecyl sulphate (SDS) as an ionic surfactant and (2) thermal treatment in an oven operated at 850°C. Batch adsorption tests were carried out on removing MBD from aqueous solution using the above-mentioned bentonites. It was found that the effectiveness of bentonites towards MBD removal was in the following order: thermal-bentonite > SDS-bentonite > natural bentonite. X-Ray diffraction analysis showed that an increase in the microscopic bentonite platelets on treatment with SDS was the reason behind the higher uptake of MBD. An increase in sorbent concentration or initial pH value of the solutions resulted in a greater removal of MBD from the solution. An increase in temperature led to an increase in MBD uptake by the bentonites studied in this work. The Freundlich isotherm model was employed and found to represent the experimental data well.

Photocatalytic Degradation of Methylene Blue over Co-Ag3VO4 under Visible Light Irradiation

2011 ◽  
Vol 335-336 ◽  
pp. 1385-1390 ◽  
Author(s):  
Shuo Wiei Zhao ◽  
Hui Xu ◽  
Hua Ming Li ◽  
Yuan Guo Xu
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Visible Light Irradiation ◽  
Absorption Edge ◽  
Diffuse Reflectance Spectroscopy ◽  
Dye Degradation ◽  
Light Irradiation ◽  
Experimental Conditions ◽  
X Ray

In order to improve the photocatalytic activity, Co was successfully loaded into Ag3VO4 by using impregnation process. The samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), energy-dispersive X-ray spectroscopy (EDS) and diffuse reflectance spectroscopy (DRS). The XRD and SEM–EDS analyses revealed that Co ion was dispersed on Ag3VO4. The DRS results indicated that the absorption edge of the Co–Ag3VO4 catalyst shifted to longer wavelength. The enhanced photocatalytic activity of Co–Ag3VO4 for Methylene Blue(MB) dye degradation under visible light irradiation was due to its wider absorption edge and higher separation rate of photo-generated electron and holes. In the experimental conditions, it is demonstrated that the MB was effectively degraded by more than 95% within 40 min when the Co–Ag3VO4 catalyst was calcined at 300°C with 1 wt.% Co content.

scholarly journals Fabrication, N-doping Mechanism and Evaluation of N-doped TiO2 Thin Films Based on Laser Ablation Method

2009 ◽  
Vol 2 (1) ◽  
pp. 17-23 ◽  
Author(s):  
S. Somekawa ◽  
Y. Kusumoto ◽  
H. Yang ◽  
M. Abdulla-Al-Mamun ◽  
B. Ahmmad
Keyword(s):  
Crystal Structure ◽  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Laser Ablation ◽  
Anatase Phase ◽  
Rutile Phase ◽  
Laser Ablation Method ◽  
Dye Decomposition ◽  
N Doping ◽  
Keywords Laser

The relation among the change of the crystal structure, the amount of doped N and the photocatalytic activity for the decomposition of methylene blue was studied. The N-doping was promoted by the change of the crystal structure from the rutile phase to the anatase phase. The photocatalytic activity for the decomposition of methylene blue was enhanced by an increase in the amount of anatase crystals and doped N. Keywords: Laser ablation; N-doping process; Crystal change; N-doped TiO2 thin film; Dye decomposition. © 2010 JSR Publications. ISSN: 2070-0237 (Print); 2070-0245 (Online). All rights reserved. DOI: 10.3329/jsr.v2i1.2992        J. Sci. Res. 2 (1), 17-23 (2010) 

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.

Study on Photocatalytic Properties of Anatase Phase TiO2 Synthesized by Ultrasonic-Assisted Hydrolysis

2012 ◽  
Vol 573-574 ◽  
pp. 110-114 ◽  
Author(s):  
Jin Xia ◽  
Ri Ya Jin ◽  
Kai Xuan Guo ◽  
Si Jing Yang
Keyword(s):  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Uv Light ◽  
Anatase Phase ◽  
Ultrasonic Method ◽  
X Ray Diffraction ◽  
Hydrolysis Method ◽  
Titanium Tetra Isopropoxide ◽  
Ultrasonic Assisted ◽  
Ft Ir

Titanium dioxide powders were synthesized by ultrasonic-assisted hydrolysis reaction of titanium tetra-isopropoxide at the low-temperature. The samples were characterized by Fourier transform infrared spectroscopy (FT-IR), powder X-ray diffraction (XRD). The photocatalytic activity of samples were investigated by the degradation of methyl orange under UV light radiation (6W, λ= 352nm) at room temperature. The results indicated that the products were mainly composed of high homogeneity anatase phases, and the methyl orange degradation rate can reach more than 90% under ultraviolet irradiation 180min. The photocatalytic activity of the samples prepared by ultrasonic method is higher than that of the samples prepared by conventional hydrolysis method.

Effect of pH on the Properties of BiVO4 by Hydrothermal Synthesis Method

2018 ◽  
Vol 281 ◽  
pp. 813-818 ◽  
Author(s):  
Xin Liu ◽  
Jia Ke Li
Keyword(s):  
Methylene Blue ◽  
Raw Materials ◽  
Synthesis Method ◽  
Precursor Solution ◽  
X Ray Diffraction ◽  
Synthetic Sample ◽  
Photocatalytic Ability ◽  
Synthetic Product ◽  
Strong Adsorption ◽  
Blue Solution

Bismuth vanadate (BiVO4 ) powders were synthesized using Bi (NO3)3.5H2O and NH4VO3 as raw materials, NaOH and HNO3 for pH adjustment. The samples were characterized by X-ray diffraction ( XRD ), scanning electron microscopy (SEM ) and UV-vis diffuse reflectance spectra techniques. The results show that the pH of precursor solution has great effect on the composition and morphology of products. Synthetic product was BiVO4 with two kinds of crystal shape ( monoclinic and tetragonal ) with pH of 3; synthetic product was pure monoclinic phase BiVO4 when the pH is between 5-9. Whereas, V2O5 and Bi2O3 appeared when the pH was 11; synthetic product was a mixture of V2O5 and Bi2O3 with pH of 13, and BiVO4 don’t exist. The photocatalytic activity was evaluated by the degradation of methylene blue solution. It is shown that the synthetic sample has the best photocatalytic ability with pH of 5. The degradation of methylene blue reaches 84.7% when irradiated for 240 min by high pressure mercury lamp, and the sample synthesized at 13 for pH has strong adsorption capacity and poor photocatalytic ability.

scholarly journals Hydrothermal Synthesis of rGO-TiO2 Composites as High-Performance UV Photocatalysts for Ethylparaben Degradation

Catalysts ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 520 ◽  
Author(s):  
Miller Ruidíaz-Martínez ◽  
Miguel A. Álvarez ◽  
María Victoria López-Ramón ◽  
Guillermo Cruz-Quesada ◽  
José Rivera-Utrilla ◽  
...  
Keyword(s):  
High Performance ◽  
Photocatalytic Performance ◽  
Raw Materials ◽  
Anatase Phase ◽  
Titanium Isopropoxide ◽  
Rutile Phase ◽  
Pure Tio2 ◽  
New Materials ◽  
Reduced Graphene ◽  
Structural Surface

A series of reduced graphene oxide-TiO2 composites (rGO-TiO2) were prepared by hydrothermal treatment using graphite and titanium isopropoxide as raw materials. The structural, surface, electronic, and optical properties of the prepared composites were extensively characterized by N2 adsorption, FTIR, XRD, XPS, Raman spectroscopy, and DRS. GO was found to be effectively reduced and TiO2 to be in pure anatase phase in all composites obtained. Finally, experiments were performed to evaluate the effectiveness of these new materials as photocatalysts in the degradation of ethylparaben (EtP) by UV radiation. According to the band-gap energies obtained (ranging between 3.09 eV for 4% rGO-TiO2 to 2.55 eV for 30% rGO-TiO2), the rGO-TiO2 composites behave as semiconductor materials. The photocatalytic activity is highest with a rGO content of 7 wt% (7% rGO-TiO2), being higher than observed for pure TiO2 (Eg = 3.20 eV) and achieving 98.6% EtP degradation after only 40 min of treatment. However, the degradation yield decreases with higher percentages of rGO. Comparison with rGO-P25 composites showed that a better photocatalytic performance in EtP degradation is obtained with synthesized TiO2 (rGO-TiO2), probably due to the presence of the rutile phase (14.1 wt %) in commercial P25.

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