Synthesis, characterization and photocatalytic activity evaluation of WO3, TiO2 and WO3/TiO2 supported on zeolite faujasite

AbstractThe present investigation is focused on the preparation, characterization, and photocatalytic activity evaluation of TiO2/zeolite, WO3/zeolite, WO3/TiO2/zeolite, and WO3/TiO2 composites. Zeolite fujasite (FAU) was synthesized by the hydrothermal method, while the semiconductor/zeolite composites by a straightforward physical mixture and calcination treatment. The photocatalytic activity of the materials was evaluated through the methyl orange (MO) degradation under near-UV irradiation (365 nm). The photocatalysts were characterized by X-ray diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscope (SEM), Energy-dispersive X-ray Spectroscopy (EDX), UV–vis diffuse reflectance spectroscopy and nitrogen physisorption. Results indicated that TiO2, WO3, and Zeolite Y kept their crystalline phases after the preparation method. TiO2 and WO3 particles were distributed on zeolite surface. Also, no significant changes in the band gap energies of the photocatalysts were found. The surface area of zeolite FAU decreased with the addition of TiO2 and WO3. The best MO degradation under near-UV irradiation was obtained with WO3/TiO2 heterojunction and TiO2 P25, no synergistic effect was found between semiconductors and zeolite FAU. Additionally, the kinetic data of the photocatalytic elimination of MO with all photocatalysts under near-UV radiation was investigated with several models: Zero-order, First-Order, Second Order, Modified Freundlich and Parabolic Diffusion, they were consistent with Modified Freundlich model. The effect of initial pH and photocatalyst weight was explored for TiO2/Zeolite composite and it was found that the best MO degradation was obtained at natural pH of 10.3 and 0.2 g of composite was the optimal amount of photocatalyst. Finally, the positive hole formation in all photocatalysts was detected by UV–vis spectroscopy and it was discovered that the highest density of positive holes was obtained with TiO2/zeolite composite.

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Photocatalytic Degradation of Estriol Using Iron-Doped TiO2 under High and Low UV-Irradiation

10.20944/preprints201809.0583.v1 ◽

2018 ◽

Author(s):

Irwing M. Ramírez-Sánchez ◽

Erick R. Bandala

Keyword(s):

Photocatalytic Activity ◽

Electron Microscope ◽

Uv Irradiation ◽

Photoelectron Spectroscopy ◽

Diffuse Reflectance Spectroscopy ◽

Bet Surface Area ◽

Doped Tio2 ◽

X Ray ◽

Transmission Electron ◽

Iron Doped

Iron Doped TiO2 nanoparticles (Fe-TiO2) were synthesized and photocatalitically investigated under high and low fluence values of UV-radiation. The Fe-TiO2 physical characterization was performed using X-ray Powder Diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area analysis, Transmission Electron Microscope (TEM), Scanning Electron Microscope (SEM), Diffuse Reflectance Spectroscopy (DRS), and X-Ray Photoelectron Spectroscopy (XPS) technique. The XPS evidenced that ferric ion (Fe3+) was in the lattice of TiO2 and co-dopants no intentionally added were also present due to the precursors of the synthetic method. The Fe3+ concentration played a key role in the photocatalytic generation of hydroxyl radical (•OH) and estriol (E3) degradation. Fe-TiO2 materials accomplished E3 degradation, and it was found that the catalyst with 0.3 at. % content of Fe (0.3 Fe-TiO2) enhanced the photocatalytic activity under low UV-irradiation compared with no intentionally Fe-added TiO2 (zero-iron TiO2) and Aeroxide® TiO2 P25. Furthermore, the enhanced photocatalytic activity of 0.3 Fe-TiO2 under low UV-irradiation may have applications when radiation intensity must be controlled, as in medical applications, or when strong UV absorbing species are present in water.

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Photocatalytic Degradation of Estriol Using Iron-Doped TiO2 under High and Low UV Irradiation

Catalysts ◽

10.3390/catal8120625 ◽

2018 ◽

Vol 8 (12) ◽

pp. 625 ◽

Cited By ~ 11

Author(s):

Irwing Ramírez-Sánchez ◽

Erick Bandala

Keyword(s):

Electron Microscopy ◽

Photocatalytic Activity ◽

Uv Irradiation ◽

Photoelectron Spectroscopy ◽

Diffuse Reflectance Spectroscopy ◽

Bet Surface Area ◽

Doped Tio2 ◽

X Ray ◽

Tio2 Lattice ◽

Iron Doped

Iron-doped TiO2 nanoparticles (Fe-TiO2) were synthesized and photocatalitically investigated under high and low fluence values of UV radiation. The Fe-TiO2 physical characterization was performed using X-ray Powder Diffraction (XRD), Brunauer–Emmett–Teller (BET) surface area analysis, Transmission Electron Microscopy (TEM), Scanning Electron Microscopy (SEM), Diffuse Reflectance Spectroscopy (DRS), and X-ray Photoelectron Spectroscopy (XPS). The XPS evidenced that the ferric ion (Fe3+) was in the TiO2 lattice and unintentionally added co-dopants were also present because of the precursors of the synthetic method. The Fe3+ concentration played a key role in the photocatalytic generation of hydroxyl radicals (•OH) and estriol (E3) degradation. Fe-TiO2 accomplished E3 degradation, and it was found that the catalyst with 0.3 at.% content of Fe (0.3 Fe-TiO2) enhanced the photocatalytic activity under low UV irradiation compared with TiO2 without intentionally added Fe (zero-iron TiO2) and Aeroxide® TiO2 P25. Furthermore, the enhanced photocatalytic activity of 0.3 Fe-TiO2 under low UV irradiation may have applications when radiation intensity must be controlled, as in medical applications, or when strong UV absorbing species are present in water.

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Photocatalytic activity of Pr-modified TiO2 for the degradation of bisphenol A

SN Applied Sciences ◽

10.1007/s42452-021-04284-2 ◽

2021 ◽

Vol 3 (2) ◽

Author(s):

Denise S. Cordeiro ◽

Fernando L. Cassio ◽

Larissa Ciccotti ◽

Thiago L. R. Hewer ◽

Paola Corio ◽

...

Keyword(s):

Photocatalytic Activity ◽

Bisphenol A ◽

Pore Diameter ◽

Sol Gel ◽

Bandgap Energy ◽

Photocatalytic Efficiency ◽

Average Pore ◽

X Ray ◽

Vis Spectroscopy ◽

Adsorption Desorption

AbstractPraseodymium doped TiO2 nanoparticles were successfully prepared by the sol–gel method and characterized by X-ray powder diffraction, N2 adsorption–desorption isotherm, and UV–vis spectroscopy. The effects of the dopant on the crystallite size, specific surface area, average pore diameter, pore volume, and bandgap energy were investigated. The photocatalytic activity of the catalysts was evaluated by bisphenol A degradation and mineralization, which is a representative endocrine disruptor. Furthermore, under visible light irradiation the Pr-modified TiO2 photocatalysts exhibited higher photocatalytic efficiency than unmodified TiO2. When praseodymium was loaded (1.0–5.0%) onto the surface of TiO2, the rates of degradation and mineralization were increased 3–5 times.

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Enhanced Photocatalytic Activity of CuWO4 Doped TiO2 Photocatalyst Towards Carbamazepine Removal under UV Irradiation

Separations ◽

10.3390/separations8030025 ◽

2021 ◽

Vol 8 (3) ◽

pp. 25

Author(s):

Chukwuka Bethel Anucha ◽

Ilknur Altin ◽

Emin Bacaksız ◽

Tayfur Kucukomeroglu ◽

Masho Hilawie Belay ◽

...

Keyword(s):

Electron Microscopy ◽

Photocatalytic Activity ◽

Photoelectron Spectroscopy ◽

Diffuse Reflectance Spectroscopy ◽

Sol Gel ◽

Pure Tio2 ◽

Component Part ◽

Energy Yield ◽

Mechanical Agitation ◽

X Ray

Abatement of contaminants of emerging concerns (CECs) in water sources has been widely studied employing TiO2 based heterogeneous photocatalysis. However, low quantum energy yield among other limitations of titania has led to its modification with other semiconductor materials for improved photocatalytic activity. In this work, a 0.05 wt.% CuWO4 over TiO2 was prepared as a powder composite. Each component part synthesized via the sol-gel method for TiO2, and CuWO4 by co-precipitation assisted hydrothermal method from precursor salts, underwent gentle mechanical agitation. Homogenization of the nanopowder precursors was performed by zirconia ball milling for 2 h. The final material was obtained after annealing at 500 °C for 3.5 h. Structural and morphological characterization of the synthesized material has been achieved employing X-ray diffraction (XRD), Fourier transform infra-red (FTIR) spectroscopy, Brunauer–Emmett–Teller (BET) N2 adsorption–desorption analysis, Scanning electron microscopy-coupled Energy dispersive X-ray spectroscopy (SEM-EDS), Transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and UV-Vis diffuse reflectance spectroscopy (UV-vis DRS) for optical characterization. The 0.05 wt.% CuWO4-TiO2 catalyst was investigated for its photocatalytic activity over carbamazepine (CBZ), achieving a degradation of almost 100% after 2 h irradiation. A comparison with pure TiO2 prepared under those same conditions was made. The effect of pH, chemical scavengers, H2O2 as well as contaminant ion effects (anions, cations), and humic acid (HA) was investigated, and their related influences on the photocatalyst efficiency towards CBZ degradation highlighted accordingly.

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Study of the Effect of TiO2 Layer on the Adsorption and Photocatalytic Activity of TiO2-MoS2 Heterostructures under Visible-Infrared Light

International Journal of Photoenergy ◽

10.1155/2020/8740825 ◽

2020 ◽

Vol 2020 ◽

pp. 1-9 ◽

Cited By ~ 2

Author(s):

N. Cruz-González ◽

O. Calzadilla ◽

J. Roque ◽

F. Chalé-Lara ◽

J. K. Olarte ◽

...

Keyword(s):

Electron Microscopy ◽

Photocatalytic Activity ◽

Photoelectron Spectroscopy ◽

Diffuse Reflectance Spectroscopy ◽

Nitrogen Adsorption ◽

High Photocatalytic Activity ◽

Infrared Light ◽

Polluted Water ◽

Light Spectrum ◽

X Ray

In the last decade, the urgent need to environmental protection has promoted the development of new materials with potential applications to remediate air and polluted water. In this work, the effect of the TiO2 thin layer over MoS2 material in photocatalytic activity is reported. We prepared different heterostructures, using a combination of electrospinning, solvothermal, and spin-coating techniques. The properties of the samples were analyzed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), atomic force microscopy (AFM), X-ray diffraction (XRD), nitrogen adsorption-desorption isotherms, UV-Vis diffuse reflectance spectroscopy (UV-Vis-DRS), and X-ray photoelectron spectroscopy (XPS). The adsorption and photocatalytic activity were evaluated by discoloration of rhodamine B solution. The TiO2-MoS2/TiO2 heterostructure presented three optical absorption edges at 1.3 eV, 2.28 eV, and 3.23 eV. The high adsorption capacity of MoS2 was eliminated with the addition of TiO2 thin film. The samples show high photocatalytic activity in the visible-IR light spectrum.

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Study on Synthesis and Photocatalytic Activity of Porous Titania Nanotubes

Advances in Materials Science and Engineering ◽

10.1155/2016/3532817 ◽

2016 ◽

Vol 2016 ◽

pp. 1-10 ◽

Cited By ~ 2

Author(s):

Huang Liu ◽

Yanhua Zhang ◽

Hongtao Yang ◽

Wei Xiao ◽

Lanlan Sun

Keyword(s):

Electron Microscopy ◽

Photocatalytic Activity ◽

Filter Paper ◽

Photoelectron Spectroscopy ◽

Diffuse Reflectance Spectroscopy ◽

Cellulose Nanofibers ◽

Titania Nanotubes ◽

Tetrabutyl Titanate ◽

X Ray ◽

Porous Titania

Using the common natural cellulose substance (filter paper) and triblock copolymer (Pluronic P123) micelles as dual templates, porous titania nanotubes with enhanced photocatalytic activity have been successfully synthesized through sol-gel methods. Firstly, P123 micelles were adsorbed onto the surfaces of cellulose nanofibers of filter paper, followed by hydrolysis and condensation of tetrabutyl titanate around these micelles to form titania layer. After calcination to remove the organic templates, hierarchical titania nanotubes with pores in the walls were obtained. The sample was characterized by X-ray diffraction pattern (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen adsorption/desorption, Fourier Transform Infrared Spectroscopy (FT-IR), Ultraviolet-Visible Diffuse Reflectance Spectroscopy (UV-Vis DRS), and X-ray photoelectron spectroscopy (XPS). As compared with commercial P25 catalyst, the porous titania nanotubes prepared by this method displayed significantly enhanced photocatalytic activity for degrading methyl orange under UV irradiation. Within 10 minutes, the porous titania nanotubes are able to degrade over 70% of the original MO, while the value for the commercial Degussa P25 is only about 33%.

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

Advanced Materials Research ◽

10.4028/www.scientific.net/amr.335-336.1385 ◽

2011 ◽

Vol 335-336 ◽

pp. 1385-1390 ◽

Cited By ~ 1

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.

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Enhanced visible-active photocatalytic behaviors observed in Mn-doped BiFeO3

Modern Physics Letters B ◽

10.1142/s0217984918501853 ◽

2018 ◽

Vol 32 (17) ◽

pp. 1850185 ◽

Cited By ~ 5

Author(s):

Yun-Hui Si ◽

Yu Xia ◽

Ya-Yun Li ◽

Shao-Ke Shang ◽

Xin-Bo Xiong ◽

...

Keyword(s):

Photocatalytic Activity ◽

Visible Light ◽

Band Gap ◽

Diffuse Reflectance Spectroscopy ◽

X Ray Diffraction ◽

Electron Hole ◽

X Ray ◽

Mn Doped ◽

Hole Recombination ◽

Narrow Band Gap Semiconductors

A series of BiFeO3 and BiFe[Formula: see text]Mn[Formula: see text]O3 (x = 0, 0.02, 0.04, 0.06, 0.08, 0.10) were synthesized by a hydrothermal method. The samples were characterized by X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy (EDS) and UV–Vis diffuse reflectance spectroscopy, and their photocatalytic activity was studied by photocatalytic degradation of methylene blue in aqueous solution under visible light irradiation. The band gap of BiFeO3 was significantly decreased from 2.26 eV to 1.90 eV with the doping of Mn. Furthermore, the 6% Mn-doped BiFeO3 photocatalyst exhibited the best activity with a degradation rate of 94% after irradiation for 100 min. The enhanced photocatalytic activity with Mn doping could be attributed to the enhanced optical absorption, increment of surface reactive sites and reduction of electron–hole recombination. Our results may be conducive to design more efficient photocatalysts responsive to visible light among narrow band gap semiconductors.

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Visible-Light-Induced Photocatalytic Activity of Boron-Doped BiVO4

Materials Science Forum ◽

10.4028/www.scientific.net/msf.809-810.890 ◽

2014 ◽

Vol 809-810 ◽

pp. 890-894

Author(s):

Dan Li ◽

Lian Wei Shan ◽

Gui Lin Wang ◽

Li Min Dong ◽

Wei Li ◽

...

Keyword(s):

Photocatalytic Activity ◽

Visible Light ◽

Diffuse Reflectance ◽

Diffuse Reflectance Spectroscopy ◽

Sol Gel ◽

Reflectance Spectroscopy ◽

Scheelite Structure ◽

X Ray Diffraction ◽

X Ray ◽

Boron Doped

Boron-BiVO4 samples were synthesized by sol-gel method. They were characterized by UV-vis diffuse reflectance spectroscopy, X-ray diffraction. Photocatalytic activity of the obtained BiVO4 samples was investigated through degrading methylene blue (MB). The results reveal that boron-BiVO4 catalysts have monoclinic scheelite structure. The BiVO4 and Co-BiVO4 photocatalysts were responsive to visible light. Co-BiVO4 photocatalyst showed higher photocatalytic activity than pure BiVO4, resulting in the significantly improved efficiency of degradation of MB.

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Hydrothermal Synthesis of Iodine-Doped Nanoplates with Enhanced Visible and Ultraviolet-Induced Photocatalytic Activities

International Journal of Photoenergy ◽

10.1155/2012/915386 ◽

2012 ◽

Vol 2012 ◽

pp. 1-12 ◽

Cited By ~ 5

Author(s):

Jiang Zhang ◽

Zheng-Hong Huang ◽

Yong Xu ◽

Feiyu Kang

Keyword(s):

Photocatalytic Activity ◽

Photoelectron Spectroscopy ◽

Oxygen Vacancies ◽

Diffuse Reflectance Spectroscopy ◽

Synergetic Effect ◽

X Ray Diffraction ◽

X Ray ◽

Selected Area Electron Diffraction ◽

Transmission Electron ◽

Photocatalytic Activities

The iodine-doped Bi2WO6(I-BWO) photocatalyst was prepared via a hydrothermal method using potassium iodide as the source of iodine. The samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscopy (TEM) and selected area electron diffraction (SAED), X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS), and photoluminescence (PL) spectroscopy. The photocatalytic activity of I-BWO for the degradation of rhodamine B (RhB) was higher than that of pure BWO and I2-BWO regardless of visible light (>420 nm) or ultraviolet light (<400 nm) irradiation. The results of DRS analysis showed that the I-BWO and I2-BWO catalysts had narrower band gaps. XPS analysis proved that the multivalent iodine species including I0and were coadsorbed on the defect surface of Bi2WO6in I-BWO. The enhanced PL intensity revealed that a large number of defects of oxygen vacancies were formed by the doping of iodine. The enhanced photocatalytic activity of I-BWO for degradation of RhB was caused by the synergetic effect of a small crystalline size, a narrow band gap, and plenty of oxygen vacancies.

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