scholarly journals Sonochemical Synthesis of Ce-doped TiO2 Nanostructure: A Visible-Light-Driven Photocatalyst for Degradation of Toluene and O-Xylene

Materials ◽  
2019 ◽  
Vol 12 (8) ◽  
pp. 1265 ◽  
Author(s):  
Lee ◽  
Choi
Keyword(s):  
Surface Area ◽  
Light Source ◽  
Photoelectron Spectroscopy ◽  
Photocatalytic Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
Pure Tio2 ◽  
Doped Tio2 ◽  
White Leds ◽  
Daylight Lamp ◽  
Gaseous Toluene

Ce-doped TiO2 nanostructures (CeT) with different amounts of Ce (0.5, 0.75, 1.0, 1.5, and 2.0 wt.%) were synthesized using a sonochemical processing method. The physicochemical properties of the prepared samples were explored using UV-visible diffuse reflectance spectroscopy (UV-vis DRS), field-emission TEM (FE-TEM), XRD, X-ray photoelectron spectroscopy (XPS), photoluminescence spectroscopy (PL), and surface area and pore size analyzers. The photocatalytic performance of the prepared CeT was assessed by monitoring their degradation efficiencies for gaseous toluene and o-xylene—widely known as significant indoor air pollutants—under daylight irradiation. The prepared CeT exhibited significantly improved photocatalytic performance towards the degradation of toluene and o-xylene, which was much higher than that observed for pure TiO2 and commercial P25 TiO2. Particularly, photocatalytic degradation efficiencies by the prepared CeT catalysts increased remarkably in the case of o-xylene (up to 99.4%) compared to toluene (up to 49.1%). The degradation efficiency by the CeT was greatest for the CeT-0.75 sample, followed by, in order, CeT-1.0, CeT-0.5, CeT-1.5, and CeT-2.0 samples in agreement with the order of the surface area and the particle size of the catalysts. According to the change of light source, the average decomposition efficiencies for toluene and o-xylene by CeT-0.75 were shown in the order of conventional daylight lamp > violet light emitting diodes (LEDs) > white LEDs. The decomposition efficiencies normalized to supplied electric power, however, were estimated to be in the following order of violet LEDs > white LEDs > conventional daylight lamp, indicating that the LEDs could be a much more energy efficient light source for the photodecomposition of target toluene and o-xylene using the CeT-0.75 photocatalyst.

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

Separations ◽  
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.

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

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.

scholarly journals Synthesis, Characterization, and Photocatalytic Evaluation of Manganese (III) Phthalocyanine Sensitized ZnWO4 (ZnWO4MnPc) for Bisphenol A Degradation under UV Irradiation

Nanomaterials ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 2139 ◽  
Author(s):  
Chukwuka Bethel Anucha ◽  
Ilknur Altin ◽  
Zekeriya Biyiklioglu ◽  
Emin Bacaksiz ◽  
Ismail Polat ◽  
...  
Keyword(s):  
Bisphenol A ◽  
Uv Irradiation ◽  
Photoelectron Spectroscopy ◽  
Photocatalytic Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
Degradation Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Uv Visible ◽  
Adsorption Desorption

ZnWO4MnPc was synthesized via a hydrothermal autoclave method with 1 wt.% manganese (iii) phthalocyanine content. The material was characterized for its structural and morphological features via X-ray diffraction (XRD) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, transmission emission microscopy (TEM), scanning electron microscopy-Energy dispersive X-ray spectroscopy (SEM-EDX), N2 adsorption–desorption at 77K, X-ray photoelectron spectroscopy (XPS), and UV-visible/diffuse reflectance spectroscopy(UV-vis/DRS). ZnWO4MnPc photocatalytic performance was tested on the degradation of bisphenol A (BPA). The ZnWO4MnPc material removed 60% of BPA after 4 h of 365 nm UV irradiation. Degradation process improved significantly to about 80% removal in the presence of added 5 mM H2O2 after 4 h irradiation. Almost 100% removal was achieved after 30 min under 450 nm visible light irradiation in the presence of same concentration of H2O2. The effect of ions and humic acid (HA) towards BPA removal was also investigated.

scholarly journals The Photocatalytic and Antibacterial Performance of Nitrogen-Doped TiO2: Surface-Structure Dependence and Silver-Deposition Effect

Nanomaterials ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 2261 ◽  
Author(s):  
Abdul Wafi ◽  
Erzsébet Szabó-Bárdos ◽  
Ottó Horváth ◽  
Mihály Pósfai ◽  
Éva Makó ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Visible Light ◽  
Surface Area ◽  
Photocatalytic Performance ◽  
Visible Region ◽  
Bet Surface Area ◽  
Doped Tio2 ◽  
X Ray ◽  
Nitrogen Doped ◽  
Visible Light Driven

Catalysts for visible-light-driven oxidative cleaning processes and antibacterial applications (also in the dark) were developed. In order to extend the photoactivity of titanium dioxide into the visible region, nitrogen-doped TiO2 catalysts with hollow and non-hollow structures were synthesized by co-precipitation (NT-A) and sol–gel (NT-U) methods, respectively. To increase their photocatalytic and antibacterial efficiencies, various amounts of silver were successfully loaded on the surfaces of these catalysts by using a facile photo-deposition technique. Their physical and chemical properties were evaluated by using scanning electron microscopy (SEM), transmission electron microscopy–energy dispersive X-ray spectroscopy (TEM–EDS), Brunauer–Emmett–Teller (BET) surface area, X-ray diffraction (XRD), and diffuse reflectance spectra (DRS). The photocatalytic performances of the synthesized catalysts were examined in coumarin and 1,4-hydroquinone solutions. The results showed that the hollow structure of NT-A played an important role in obtaining high specific surface area and appreciable photoactivity. In addition, Ag-loading on the surface of non-hollow structured NT-U could double the photocatalytic performance with an optimum Ag concentration of 10−6 mol g−1, while a slight but monotonous decrease was caused in this respect for the hollow surface of NTA upon increasing Ag concentration. Comparing the catalysts with different structures regarding the photocatalytic performance, silverized non-hollow NT-U proved competitive with the hollow NT-A catalyst without Ag-loading for efficient visible-light-driven photocatalytic oxidative degradations. The former one, due to the silver nanoparticles on the catalyst surface, displayed an appreciable antibacterial activity, which was comparable to that of a reference material practically applied for disinfection in polymer coatings.

scholarly journals Porous V2O5/TiO2 Nanoheterostructure Films with Enhanced Visible-Light Photocatalytic Performance Prepared by the Sparking Method

Molecules ◽  
2020 ◽  
Vol 25 (15) ◽  
pp. 3327
Author(s):  
Porntipa Pooseekheaw ◽  
Winai Thongpan ◽  
Arisara Panthawan ◽  
Ekkapong Kantarak ◽  
Wattikon Sroila ◽  
...  
Keyword(s):  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Photocatalytic Performance ◽  
Composite Films ◽  
Cost Effective ◽  
Atomic Ratio ◽  
Pure Tio2 ◽  
Sem Images ◽  
Transmission Electron ◽  
Highly Correlated

Porous V2O5/TiO2 nanoheterostructure films with different atomic ratios of Ti/V (4:1, 2:1, 1:1, and 1:2) were synthesized by a sparking method for the first time. The sparking method, which is a simple and cost-effective process, can synthesize highly porous and composite films in one step. Field-emission scanning electron microscope (FE-SEM) images revealed the porosity morphology of all prepared samples. V2O5/TiO2 nanoheterostructure films were confirmed by Raman spectroscopy, high-resolution transmission electron microscopy (HRTEM), and X-ray photoelectron spectroscopy (XPS). The secondary particle size and band gap of the samples were highly correlated to the V2O5 proportion, resulting in enhanced visible-light absorbance. V2O5/TiO2 nanoheterostructure films at an atomic ratio of 1:1 showed the highest photocatalytic performance, which improved the degradation rate up to 24% compared to pure TiO2 film. It is believed that the formed nanoheterostructure and greater portion of V4+ ions are reflected by this ratio.

scholarly journals Enhanced Photocatalytic Performance and Mechanism of Au@CaTiO3 Composites with Au Nanoparticles Assembled on CaTiO3 Nanocuboids

Micromachines ◽  
2019 ◽  
Vol 10 (4) ◽  
pp. 254 ◽  
Author(s):  
Yuxiang Yan ◽  
Hua Yang ◽  
Zao Yi ◽  
Ruishan Li ◽  
Xiangxian Wang
Keyword(s):  
Photoelectron Spectroscopy ◽  
Photocatalytic Performance ◽  
Au Nanoparticles ◽  
Diffuse Reflectance Spectroscopy ◽  
Localized Surface Plasmon ◽  
Hydrothermal Route ◽  
Electron Hole ◽  
Photoexcited Electron ◽  
Au Nps ◽  
X Ray

Using P25 as the titanium source and based on a hydrothermal route, we have synthesized CaTiO3 nanocuboids (NCs) with the width of 0.3–0.5 μm and length of 0.8–1.1 μm, and systematically investigated their growth process. Au nanoparticles (NPs) of 3–7 nm in size were assembled on the surface of CaTiO3 NCs via a photocatalytic reduction method to achieve excellent Au@CaTiO3 composite photocatalysts. Various techniques were used to characterize the as-prepared samples, including X-ray powder diffraction (XRD), scanning/transmission electron microscopy (SEM/TEM), diffuse reflectance spectroscopy (UV-vis DRS), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). Rhodamine B (RhB) in aqueous solution was chosen as the model pollutant to assess the photocatalytic performance of the samples separately under simulated-sunlight, ultraviolet (UV) and visible-light irradiation. Under irradiation of all kinds of light sources, the Au@CaTiO3 composites, particularly the 4.3%Au@CaTiO3 composite, exhibit greatly enhanced photocatalytic performance when compared with bare CaTiO3 NCs. The main roles of Au NPs in the enhanced photocatalytic mechanism of the Au@CaTiO3 composites manifest in the following aspects: (1) Au NPs act as excellent electron sinks to capture the photoexcited electrons in CaTiO3, thus leading to an efficient separation of photoexcited electron/hole pairs in CaTiO3; (2) the electromagnetic field caused by localized surface plasmon resonance (LSPR) of Au NPs could facilitate the generation and separation of electron/hole pairs in CaTiO3; and (3) the LSPR-induced electrons in Au NPs could take part in the photocatalytic reactions.

Enhancement of the Photocatalytic Performance of Ru-Doped TiO2 Nanoparticles

2008 ◽  
Vol 55-57 ◽  
pp. 853-856 ◽  
Author(s):  
Khatcharin Wetchakun ◽  
Natda Wetchakun ◽  
Sukon Phanichphant
Keyword(s):  
Electron Microscopy ◽  
Formic Acid ◽  
Tio2 Nanoparticles ◽  
Photocatalytic Performance ◽  
Condensation Reaction ◽  
Pure Tio2 ◽  
Absolute Ethanol ◽  
Impregnation Method ◽  
Doped Tio2 ◽  
Degussa P25

Pure TiO2 nanoparticles were synthesized by the modified sol-gel method using titanium tetraisopropoxide (TTIP) precursor dissolved in absolute ethanol. A pouch type cellophane membrane was employed as barrier between the precursor solution and the mixture of absolute ethanol (1:1 v/v) and distilled water with 0.5-1.0 % concentrated of ammonia in order to fix the reaction activity inside the pouch and control diffusion rate of hydrolysis and condensation reaction. The doping of TiO2 nanoparticles with 0.1, 0.2, 0.5, 1.0 and 2.0 at.% Ru was performed by the impregnation method using ruthenium acetyl acetonate in toluene as dopant. The properties of the all samples were characterized by X-ray diffraction (XRD), Brunauer, Emmett and Teller (BET)-specific surface area, Scanning electron microscopy-Energy dispersive spectroscopy (SEM-EDS) and transmission electron microscopy (TEM). The crystalline size of pure TiO2 and Ru-doped TiO2 nanopaticles were found to be in the range of 10-20 nm. The photocatalytic mineralization of formic acid, oxalic acid, sucrose and glucose was investigated using Degussa P25, pure TiO2 and Ru-doped TiO2 nanoparticles as photocatalysts in aqueous solutions under UVA irradiation. The rate of 50% mineralization of formic acid by 0.1 at.% Ru-doped TiO2 was 1.53 times and 1.34 times higher than that of pure TiO2 and Degussa P25, respectively showing the enhancement of the photocatalytic performance of TiO2 by doping with an optimum amount of ruthenium.

scholarly journals Kinetics of Highly Active TiO2 Microspheres Formation in a Presence of Ethylammonium Nitrate Ionic Liquid

2018 ◽  
Author(s):  
Anna Gołąbiewska ◽  
Micaela Checa-Suárez ◽  
Marta Paszkiewicz-Gawron ◽  
Wojciech Lisowski ◽  
Edyta Raczuk ◽  
...  
Keyword(s):  
Ionic Liquid ◽  
Surface Area ◽  
Photoelectron Spectroscopy ◽  
High Efficiency ◽  
Diffuse Reflectance Spectroscopy ◽  
Phenol Degradation ◽  
Bet Surface Area ◽  
Synthesis Time ◽  
X Ray ◽  
Highly Active

Spherical microparticles of TiO2 were synthesized by the ionic liquid-assisted solvothermal method at different reaction time (3, 6, 12 and 24h). The properties of the prepared photocatalysts were investigated by means of UV-vis diffuse-reflectance spectroscopy (DRS), BET surface area measurements, scanning electron microscopy (SEM), X-ray diffraction analysis (XRD), and X-ray photoelectron spectroscopy (XPS). The results indicated that the efficiency of phenol degradation was related with a time of the solvothermal synthesis as determined for TiO2_EAN(1:1)_24h sample. Microparticles of TiO2_EAN(1:1)_3h formed during the only 3h of synthesis time revealed really high photoactivity under visible irradiation – 75%. This value increased to 80% and 82% after 12h and 24h, respectively. The photoactivity increase was accompanied by the increase of the specific surface area thus pores size, as well as ability to absorb UV-vis irradiation. The high efficiency of phenol degradation of IL-TiO2 photocatalysts was ascribed to the interaction between the surface of TiO2 and ionic liquid components (carbon and nitrogen).

Synthesis of Hexahydroxy Strontium Stannate/Tin Dioxide Nanocomposites and Their Photocatalytic Properties for Gentian Violet

2021 ◽  
Vol 14 ◽  
Author(s):  
C.H. Yu ◽  
Z.Y. Xue ◽  
Y.J. Mao ◽  
J. F. Huang ◽  
F.H. Tao ◽  
...  
Keyword(s):  
Hydrothermal Method ◽  
Photoelectron Spectroscopy ◽  
Tin Dioxide ◽  
Photocatalytic Performance ◽  
Diffuse Reflectance Spectroscopy ◽  
Irradiation Time ◽  
Gentian Violet ◽  
Human Beings ◽  
X Ray ◽  
Strontium Stannate

Background: Gentian violet dye released from industries into the environment has caused serious water pollution and is a significant environment pollutant to human beings owing to the toxicity. It is urgent to decrease the environmental pollution by removing gentian violet in the wastewater. Objective: The aim is to synthesize hexahydroxy strontium stannate/tin dioxide nanocomposites by a simple hydrothermal method without surfactants and research the photocatalytic performance for gentian violet degradation. Methods: Hexahydroxy strontium stannate/tin dioxide nanocomposites have been obtained via the hydrothermal method. The structure, size, morphology and photocatalytic performance were characterized by X-ray diffraction, electron microscopy, solid ultraviolet-visible diffuse reflectance spectroscopy and X-ray photoelectron spectroscopy. Results : The nanocomposites possess oven-shaped morphology with the size of less than 100 nm and are composed of hexagonal SrSn(OH)6 and tetragonal SnO2 phases. The band gap of the nanocomposites is 3.52 eV. 10 mg hexahydroxy strontium stannate/tin dioxide nanocomposites have the ability to completely degrade 10 mL gentian violet solution with the concentration of 10 mgL-1 under 6 h ultraviolet-visible light irradiation. Hydroxyl radical, hole and superoxide radical are main species for the gentian violet photocatalytic degradation using the nanocomposites. Conclusion: The hexahydroxy strontium stannate/tin dioxide nanocomposites show good photocatalytic performance for the GV degradation. The photocatalytic performance for gentian violet degradation using the hexahydroxy strontium stannate/tin dioxide nanocomposites depends on the irradiation time and content of the nanocomposites.

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