Synthesis, characterization and photocatalytic activity of Ag–TiO2 nanoparticulate film

RSC Advances ◽  
2015 ◽  
Vol 5 (2) ◽  
pp. 1309-1314 ◽  
Author(s):  
P. V. R. K. Ramacharyulu ◽  
J. Praveen kumar ◽  
G. K. Prasad ◽  
A. R. Srivastava
Keyword(s):  
Photocatalytic Activity ◽  
Photocatalytic Degradation ◽  
Dip Coating ◽  
Nanoparticulate Film

Ag–TiO2 nanoparticulate film was synthesized by dip coating followed by adsorption and photoreduction. This film has demonstrated enhanced rate of photocatalytic degradation of MP when compared to TiO2 nanoparticulate film.

Photocatalytic degradation of methylene blue from aqueous solutions using nanopillars-TiO2 thin films: Batch reactor studies

2018 ◽  
Vol 18 (3) ◽  
pp. 81-91 ◽  
Author(s):  
C. Lalhriatpuia
Keyword(s):  
Thin Films ◽  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Organic Carbon ◽  
Photocatalytic Degradation ◽  
Batch Reactor ◽  
Tio2 Thin Films ◽  
Initial Concentration ◽  
Bet Specific Surface Area ◽  
Interfering Ions

Nanopillars-TiO2 thin films was obtained on a borosilicate glass substrate with (S1) and without (S2) polyethylene glycol as template. The photocatalytic behaviour of S1 and S2 thin films was assessed inthe degradation of methylene blue (MB) dye from aqueous solution under batch reactor operations. The thin films were characterized by the SEM, XRD, FTIR and AFM analytical methods. BET specific surface area and pore sizes were also obtained. The XRD data confirmed that the TiO2 particles are in its anatase mineral phase. The SEM and AFM images indicated the catalyst is composed with nanosized pillars of TiO2, evenly distributed on the surface of the substrate. The BET specific surface area and pore sizes of S1 and S2 catalyst were found to be 5.217 and 1.420 m2/g and 7.77 and 4.16 nm respectively. The photocatalytic degradation of MB was well studied at wide range of physico-chemical parameters. The effect of solution pH (pH 4.0 to 10.0) and MB initial concentration (1.0 to 10.0 mg/L) was extensively studied and the effect of several interfering ions, i.e., cadmium nitrate, copper sulfate, zinc chloride, sodium chloride, sodium nitrate, sodium nitrite, glycine, oxalic acid and EDTA in the photocatalytic degradation of MB was demonstrated. The maximum percent removal of MB was observed at pH 8.0 beyond which it started decreasing and a low initial concentration of the pollutant highly favoured the photocatalytic degradation using thin films and the presence of several interfering ions diminished the photocatalytic activity of thin films to some extent. The overall photocatalytic activity was in the order: S2 > S1 > UV. The photocatalytic degradation of MB was followed the pseudo-first-order rate kinetics. The mineralization of MB was studied with total organic carbon measurement using the TOC (total organic carbon) analysis.

Use of Nanopillars-TiO2 Thin Films in the Photocatalytic Degradation of Bromophenol Blue from Aqueous Solution

2018 ◽  
Vol 6 (1) ◽  
pp. 22-30
Author(s):  
C. Lalhriatpuia ◽  
◽  
Thanhming liana ◽  
K. Vanlaldinpuia
Keyword(s):  
Thin Films ◽  
Aqueous Solution ◽  
Photocatalytic Activity ◽  
Photocatalytic Degradation ◽  
Batch Reactor ◽  
Bromophenol Blue ◽  
Tio2 Thin Films ◽  
Initial Concentration ◽  
Bet Specific Surface Area ◽  
Interfering Ions

The photocatalytic activity of Nanopillars-TiO2 thin films was assessed in the degradation of Bromophenol blue (BPB) dye from aqueous solution under batch reactor operations. The thin films were characterized by the XRD, SEM and AFM analytical methods. BET specific surface area and pore sizes were also obtained. The XRD data showed anatase phase of TiO2 particles with average particle size of 25.4 and 21.9 nm, for S1 and S2 catalysts respectively. The SEM and AFM images indicated the catalyst composed with Nanosized pillars of TiO2, evenly distributed on the surface of the substrate. The average height of the pillars was found to be 180 and 40 nm respectively for the S1 and S2 catalyst. The BET specific surface area and pore sizes of S1 and S2 catalyst were found to be 5.217 and 1.420 m2/g and 7.77 and 4.16 nm respectively. The photocatalytic degradation of BPB using the UV light was studied at wide range of physico-chemical parametric studies to determine the mechanism of degradation as well as the practical applicability of the technique. The batch reactor operations were conducted at varied pH (pH 4.0 to 10.0), BPB initial concentration (1.0 to 20.0 mg/L) and presence of several interfering ions, i.e., cadmium nitrate, copper sulfate, zinc chloride, sodium chloride, sodium nitrate, sodium nitrite, glycine, oxalic acid and EDTA in the photocatalytic degradation of BPB. The maximum percent removal of BPB was observed at pH 6.0 and a low initial concentration of the pollutant highly favours the photocatalytic degradation using thin films. The presence of several interfering ions suppressed the photocatalytic activity of thin films to some extent. The time dependence photocatalytic degradation of BPB was demonstrated with the pseudo-first-order rate kinetics. Study was further extended with total organic carbon measurement using the TOC (Total Organic Carbon) analysis. This demonstrated an apparent mineralization of BPB from aqueous solutions.

scholarly journals Sulfur-doped CoFe2O4 nanopowders for enhanced visible-light photocatalytic activity and magnetic properties

RSC Advances ◽  
2017 ◽  
Vol 7 (80) ◽  
pp. 50546-50554 ◽  
Author(s):  
Rong Li ◽  
Chencen Sun ◽  
Jia Liu ◽  
Qiang Zhen
Keyword(s):  
Aqueous Solution ◽  
Magnetic Properties ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photocatalytic Degradation ◽  
Visible Light Photocatalytic Activity ◽  
Magnetic Recovery ◽  
Visible Light Photocatalytic

Magnetic recovery S-CoFe2O4 nanopowders showed excellent visible photocatalytic degradation of oxytetracycline and recycling performances in aqueous solution.

Photocatalytic Degradation of Methylene Blue by NiO Thin Films under Solar Light Irradiation

2019 ◽  
Vol 56 ◽  
pp. 152-157 ◽  
Author(s):  
Abdelouahab Noua ◽  
Hichem Farh ◽  
Rebai Guemini ◽  
Oussama Zaoui ◽  
Tarek Diab Ounis ◽  
...  
Keyword(s):  
Thin Films ◽  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Sol Gel ◽  
Visible Region ◽  
Optical Transmittance ◽  
Dip Coating ◽  
Light Irradiation ◽  
Solar Light ◽  
Solar Light Irradiation

Nickel oxide (NiO) thin films were successfully deposited by sol-gel dip-coating method on glass substrates. The structural, morphological and optical properties in addition to the photocatalytic activity of the prepared films were investigated. The results show that the films have a polycrystalline NiO cubic structure with dense NiO grains and average optical transmittance in the visible region. The photocatalytic properties of the films were studied through the degradation of methylene blue and 89% of degradation was achieved for 4.5h of solar light irradiation exposure which indicates the capability of NiO photocatalytic activity.

The Study on the Influential Factors of Photocatalytic Performance of Eosin-Sensitized TiO2 Nanoparticles

2013 ◽  
Vol 827 ◽  
pp. 3-7
Author(s):  
Shun Jiang He ◽  
Xue Yan Du ◽  
Qiao Wang ◽  
Jing Xu
Keyword(s):  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Photocatalytic Degradation ◽  
Degradation Rate ◽  
Photocatalytic Performance ◽  
Influential Factors ◽  
Sunlight Irradiation ◽  
Sensitization Time

The photocatalytic activity of eosin-sensitized TiO2 nanoparticles on photocatalytic degradation rate (PDR) of methyl orange under sunlight irradiation was studied. The influential factors on the degradation, such as eosin concentration, TiO2 dosage, sensitization time and sensitization temperature were also investigated. The results show that: The performance of TiO2 nanoparticles for PDR of methyl orange has been improved obviously for eosin sensitizing. The PDR of methyl orange reached 45.28% under the conditions of eosin concentration of 20mg/L, TiO2 dosage of 0.5000g/L, sensitization time of 24h and sensitization temperature of 20°C.

W-Doped TiO2 Preparation and Photocatalytic Degradation of Guaiacol

2014 ◽  
Vol 513-517 ◽  
pp. 33-36 ◽  
Author(s):  
Zi Chang Xie ◽  
Ying Wang ◽  
Peng Wang ◽  
Lei Zhang
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Photocatalytic Degradation ◽  
Degradation Rate ◽  
Amorphous State ◽  
X Ray Diffraction ◽  
Model Compounds ◽  
Plant Fibers ◽  
X Ray ◽  
Crystallite Structure

In this paper, W-doped TiO2 (W-TiO2) powder was prepared in hydrothermal method by mixing TiO2 and ammonium metatungstate. The catalysts were characterized by X-ray diffraction and ultraviolet spectrophotometer. The results displayed that W-TiO2 showed an anatase crystallite structure with 2 % W content. W-element in W-TiO2 was amorphous state. The guaiacol was degraded with the W-TiO2 in the visible light. It was a model compounds of lignin existed in the plant fibers. The degradation rate of guaiacol was increased with the photocatalytic time, as high as 88.21 % after 360 min irradiation. It was concluded that the W-TiO2 had an obvious photocatalytic activity under visible light. It can be used in the photocatalytic degradation of lignin.

scholarly journals Synthesis and Characterization of Ag@C-TiO2 Nanocomposite for Degradation of Sasirangan Textile Wastewater

2019 ◽  
Vol 22 (6) ◽  
pp. 299-304
Author(s):  
Heny Puspita Dewi ◽  
Joko Santoso ◽  
Nur Firda Trianda ◽  
Rodiansono Rodiansono
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Photocatalytic Degradation ◽  
Textile Wastewater ◽  
Band Gap Energy ◽  
Tio2 Photocatalyst ◽  
Composite Photocatalysts ◽  
Xrd Patterns ◽  
Brookite Phase

Carbon-titanium oxide nanocomposite (denoted as @C-TiO2) was successfully synthesized via hydrothermal method at 150°C for 24 h. The C-TiO2 nanocomposite was furtherly modified by adding an Ag metal dopant (denoted as Ag@C-TiO2) to improve and applied to the photocatalytic degradation of Sasirangan textile wastewater. The composite photocatalysts were characterized by XRD and UV–Vis DRS spectroscopies. XRD patterns showed that TiO2 in @C-TiO2 mainly consisted of a brookite phase, as indicated by a series sharp diffraction peak at 2θ = 27.2° (111), 31.5° (121) and 55.9° (241). The calculated band gap energy (Eg) derived from UV-Vis DRS spectra for TiO2, @C-TiO2, and Ag@C-TiO2 were 2.95 eV, 2.54 eV, and 2.74 eV, respectively. Ag@C-TiO2 photocatalyst was found to be active for the photocatalytic degradation of Sasirangan textile wastewater, as indicated by the change of wastewater color from dark to clear. The quantitative photocatalytic activity of Ag@C-TiO2 was evaluated in the degradation of methylene blue, whereas the conversion of methylene blue was 41.3%. The addition of Ag to @C-TiO2 is believed to play an essential role in the enhancement of photocatalytic activity.

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 Facile fabrication of Fe-TiO2 thin film and its photocatalytic activity

2021 ◽  
Author(s):  
Almudena Aguinaco ◽  
Beatriz Amaya ◽  
Milagrosa Ramírez-del-Solar
Keyword(s):  
Thin Films ◽  
Photocatalytic Activity ◽  
Impurity Band ◽  
Dip Coating ◽  
Molar Ratio ◽  
Material Surface ◽  
Sem Images ◽  
Xps Spectra ◽  
Oh Groups ◽  
Facile Fabrication

AbstractFe3+-TiO2 (Fe-TiO2) thin films were successfully prepared using a “sandwich” approach. TiO2 NPs were doped with different Fe3+ content (0.05%, 0.1%, 0.2% molar ratio), and the modified TiO2 NPs were deposited on glass flat support by dip coating.Structural, morphological, optical, and photocatalytic properties of Fe-TiO2 thin films were studied. XPS spectra confirm the presence of Ti, Fe, O, and defective –OH groups at the material surface. The Fe 2p spectrum demonstrates the existence of Fe3+. SEM images indicate that the incorporation of Fe3+ deforms in some degree the homogeneity of the TiO2 system. Additionally, incorporation of Fe3+ ions to the network creates an impurity band near the VB due to the oxygen vacancies, resulting in the reduction of the effective optical band gap. Photocatalytic activity of fabricated thin films in the elimination of sulfamethoxazole (SMT) follows pseudo first-order kinetics. The highest SMT removal yields were achieved using the sample with 0.05%Fe. Additionally, the use of greater thicknesses improves the removal performance. However, material detachment limits the maximum usable value around 6 µm.Finally, stability and reusability of catalysts were confirmed studying the photocatalytic activity over three cycles and evaluating that no Fe3+ leaching occurred. Graphical abstract

scholarly journals Studies on Synthesis and Characterization of Fe3O4@SiO2@Ru Hybrid Magnetic Composites for Reusable Photocatalytic Application

2022 ◽  
Vol 2022 ◽  
pp. 1-18
Author(s):  
Avvaru Praveen Kumar ◽  
Dinesh Bilehal ◽  
Tegene Desalegn ◽  
Shalendra Kumar ◽  
Faheem Ahmed ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Photocatalytic Degradation ◽  
Organic Dyes ◽  
Research Work ◽  
Magnetic Microspheres ◽  
Visible Radiation ◽  
Magnetic Composites ◽  
Acid Media ◽  
Dye Pollutants ◽  
Bet Analysis

Degradation of dye pollutants by the photocatalytic process has been regarded as the most efficient green method for removal organic dyes from contaminated water. The current research work describes the synthesis of Fe3O4@SiO2@Ru hybrid magnetic composites (HMCs) and their photocatalytic degradation of two azo dye pollutants, methyl orange (MO) and methyl red (MR), under irradiation of visible light. The synthesis of Fe3O4@SiO2@Ru HMCs involves three stages, including synthesis of Fe3O4 magnetic microspheres (MMSs), followed by silica (SiO2) coating to get Fe3O4@SiO2 MMSs, and then incorporation of presynthesized Ru nanoparticles (~3 nm) onto the surface of Fe3O4@SiO2 HMCs. The synthesized HMCs were characterized by XRD, FTIR, TEM, EDS, XPS, BET analysis, UV-DRS, PL spectroscopy, and VSM to study the physical and chemical properties. Furthermore, the narrow band gap energy of the HMC photocatalyst is a significant parameter that provides high photocatalytic properties due to the high light adsorption. The photocatalytic activity of synthesized Fe3O4@SiO2@Ru HMCs was assessed by researching their ability to degrade the aqueous solution of MO and MR dyes under visible radiation, and the influence of various functional parameters on photocatalytic degradation has also been studied. The results indicate that the photocatalytic degradation of MO and MR dyes is more than 90%, and acid media favors better degradation. The probable mechanism of photodegradation of azo dyes by Fe3O4@SiO2@Ru HMC catalysts has been proposed. Furthermore, due to the strong ferromagnetic Fe3O4 core, HMCs were easily separated from the solution after the photocatalytic degradation process for reuse. Also, the photocatalytic activity after six cycles of use is greater than 90%, suggesting the stability of the synthesized Fe3O4@SiO2@Ru HMCs.

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