scholarly journals Synthesis and Characterization of Uniform Spherical Nanoporous TiO2Aerogel Templated by Cellulose Alcohol-Gel with Enhanced Photocatalytic Activity

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
Zhiming Liu ◽  
Peng Wu ◽  
Shaoli Yang ◽  
Haiying Wang ◽  
Chunde Jin
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Thermal Method ◽  
X Ray ◽  
Double Beam ◽  
Methyl Orange Dye

The spherical nanoporous TiO2aerogels were prepared by a simple ethanol-thermal method, using spherical cellulose alcohol-gel as the template. The morphology, crystalline structure, pore size, specific surface area, and the photocatalytic activity of obtained TiO2aerogel were separately characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), N2adsorption-desorption isotherms, and double beam UV-VIS spectrophotometer. The characteristics of TiO2aerogels presented uniform sphere shape, good internal structural morphology, high specific surface area (ranging from 111.88 to 149.95 m2/g), and good crystalline anatase phase. Moreover, methyl orange dye was used as the target pollutant to characterize the photocatalytic activities and the adsorption performance. The photocatalytic experiment shows that the obtained spherical TiO2aerogels had a higher degradation ratio of 92.9% on methyl orange dye compared with aspherical TiO2aerogels prepared from other concentrations of tetrabutyl orthotitanate (TBOT).

scholarly journals Enhanced Photocatalytic Activity for Degradation of Methyl Orange over Silica-Titania

2011 ◽  
Vol 2011 ◽  
pp. 1-9 ◽  
Author(s):  
Yaping Guo ◽  
Shaogui Yang ◽  
Xuefei Zhou ◽  
Chunmian Lin ◽  
Yajun Wang ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Specific Surface ◽  
Surface Area ◽  
Calcination Temperature ◽  
Specific Surface Area ◽  
Photoelectron Spectroscopy ◽  
Anatase Phase ◽  
Solution Treatment ◽  
X Ray

Silica-modified titania (SMT) powders with different atomic ratios of silica to titanium (Rx) were successfully synthesized by a simple ultrasonic irradiation technique. The prepared samples were characterized by X-ray diffraction (XRD), FT-IR spectroscopy, transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and ultraviolet visible spectroscopy. The specific surface area was measured according to BET theory. Results indicate that the addition of silica to titania can suppress the crystalline size growth and the transformation of anatase phase to rutile phase of titania, enlarge specific surface area of the titania particles, and result in a blue shift of absorption edge compared to pure titania. The photocatalytic activity of the SMT samples was evaluated by decolorizing methyl orange aqueous solutions under UV-visible light irradiation. It was found in our study that this activity was affected by silica content, calcination temperature, H2SO4, and oxidants such as KIO4, (NH4)2S2O8and H2O2. The results reveal that the photocatalytic activity of 0.1-SMT catalyst is the best among all samples calcined at550°C for 1 h and it is 1.56 times higher than that of Degussa P-25 titania, which is a widely used commercial TiO2made by Germany Degussa company and has been most widely used in industry as photocatalyst, antiultraviolet product, and thermal stabilizer. The optimal calcination temperature for preparation was550°C. The photocatalytic activity of SMT samples is significantly enhanced by H2SO4solution treatment and oxidants.

scholarly journals Graphene Oxide Hybridised TiO2 for Visible Light Photocatalytic Degradation of Phenol

Symmetry ◽  
2020 ◽  
Vol 12 (9) ◽  
pp. 1420 ◽  
Author(s):  
Guanyu Wang ◽  
Weijie Guo ◽  
Deping Xu ◽  
Di Liu ◽  
Mengtao Qin
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Graphene Oxide ◽  
Visible Light ◽  
Specific Surface ◽  
Tio2 Nanoparticles ◽  
Surface Area ◽  
Specific Surface Area ◽  
Phenol Solution ◽  
X Ray

In industrial pollutants, phenol is a kind of degradation-resistant hazardous compound. It is generated during industrial processes in factories and treatment at sewage plants. In this study, we analyse the photocatalytic activity of TiO2 and rGO as a composite for the degradation of phenol. Hybridised titanium dioxide/reduced graphene oxide (TiO2/rGO) nanocomposites were synthesised by a simple hydrothermal method using flake graphite and tetrabutyl titanate as raw materials. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Brunauer–Emmet–Teller (BET) specific area analysis, Fourier transform infrared spectroscopy (FTIR), Raman, X-ray photoelectron spectroscopy (XPS), photoelectrochemical analysis, and UV–vis diffuse reflectance spectra (DRS) were employed to characterise the physicochemical properties of the as-prepared nanocomposites. The results showed the TiO2/rGO nanocomposites’ significant anatase phase and a small fraction of the rutile phase the same as that of the as-prepared TiO2 nanoparticles. The spherical TiO2 nanoparticles (diameter 20–50 nm) were agglomerated slightly and the agglomerates were anchored on the rGO sheets and dispersed symmetrically. The specific surface area of TiO2/rGO-4% nanocomposites was 156.4 m2/g, revealing a high specific surface area. Oxygen-containing functional groups that existed in TiO2/rGO-4% nanocomposites were almost removed during hydrothermal processing. The photocurrent response of TiO2/rGO-4% was strongest among the TiO2/rGO nanocomposites, and the bandgap of TiO2/rGO-4% was 2.91 eV, showing a redshift of absorption into the visible region, which was in favour of the high photocatalytic activity of TiO2/rGO nanocomposites under visible light (λ > 420 nm). Moreover, the samples were employed to photodegrade phenol solution under visible light irradiation. TiO2/rGO-4% nanocomposite degraded the phenol solution up to 97.9%, and its degradation rate constant was 0.0190 h−1, which had higher degradation activity than that of other TiO2/rGO nanocomposites. This is a promising candidate catalyst material for organic wastewater treatment.

scholarly journals Combination of mesoporous titanium dioxide with MoS2 nanosheets for high photocatalytic activity

2017 ◽  
Vol 19 (2) ◽  
pp. 56-60 ◽  
Author(s):  
Loghman Karimi
Keyword(s):  
Electron Microscopy ◽  
Titanium Dioxide ◽  
Photocatalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Dye Degradation ◽  
Hydrothermal Process ◽  
Bet Analysis ◽  
Mesoporous Titanium Dioxide

Abstract This study presents a facile approach for the preparation of MoS2 nanosheet decorated by porous titanium dioxide with effective photocatalytic activity. Mesoporous titanium dioxide nanostructures first synthesized by a hydrothermal process using titanium (III) chloride and then the MoS2/TiO2 were prepared through mixing of MoS2 nanosheet with mesoporous titanium dioxide under ultrasonic irradiation. The synthesized nanocomposite was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), and Brunauer-Emmett-Teller (BET) analysis. The results showed that the nanocomposite has mesoporous structure with specific surface area of 176.4 m2/g and pore diameter of 20 nm. The as-prepared MoS2/TiO2 nanocomposites exhibited outstanding photocatalytic activity for dye degradation under sunlight irradiation, which could be attributed to synergistic effect between the molybdenum disulfide nanosheet and mesoporous titanium dioxide. The photocatalytic performance achieved is about 2.2 times higher than that of mesoporous TiO2 alone. It is believed that the extended light absorption ability and the large specific surface area of the 2D MoS2 nanosheets in the nanocomposite, leading to the enhanced photocatalytic degradation activity.

scholarly journals Preparation and photocatalytic activity of the layered titanates

2010 ◽  
Vol 4 (2) ◽  
pp. 69-73 ◽  
Author(s):  
Marija Milanovic ◽  
Ivan Stijepovic ◽  
Ljubica Nikolic
Keyword(s):  
Photocatalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
High Photocatalytic Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Bet Method ◽  
Ft Ir

Titanate structures were synthesized in highly alkaline solution using hydrothermal procedure. As-prepared powders were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and transmission electron microscopy (TEM). A specific surface area of the powders was measured by BET method. Results confirmed formation of layered trititanates, already after one hour of hydrothermal synthesis. To examine the photocatalytic activity of the as-prepared layered titanates, methylene blue (MB) was employed as a target compound in response to visible light at ambient temperature. It was observed that the specific surface area, size distribution and crystallinity are important factors to get high photocatalytic activity for the decomposition of MB. .

Effects of dry grinding on pyrophyllite

Clay Minerals ◽  
1988 ◽  
Vol 23 (4) ◽  
pp. 399-410 ◽  
Author(s):  
J. L. Pérez-Rodríguez ◽  
L. Madrid Sánchez del Villar ◽  
P.J. Sánchez-Soto
Keyword(s):  
Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Grinding Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dry Grinding ◽  
Scanning Electron ◽  
Area Data

AbstractDry grinding of pyrophyllite (Hillsboro, USA) has been studied by X-ray diffraction (XRD), specific surface area measurements (BET) and scanning electron microscopy (SEM). At the beginning of the grinding process, some effects such as delamination, gliding and folding of the layers, and decrease in particle size were detected by SEM and XRD, resulting in a large increase in specific surface area, up to a maximum of ∼60 m2·g−1. Marked changes in the structure take place between 30 and 32 mins grinding. Longer grinding times increase the degree of disorder and SEM and specific surface area data suggest that aggregation occurs. XRD results indicate that some residual order persists in the degraded structure.

scholarly journals Development of a novel photocatalyst for the photocatalytic treatment of industrial wastewater

2021 ◽  
Author(s):  
Mohsen Nasirian
Keyword(s):  
Photocatalytic Activity ◽  
Transition Metal ◽  
Visible Light ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Mass Ratio ◽  
Thermal Synthesis ◽  
Composite Photocatalyst ◽  
X Ray

Heterogeneous semiconductor photocatalysts have been shown to be efficient for the degradation of refractory organics into simple compounds. Among all photocatalysts, TiO2 is the most used one. Two issues that arise with the use of unmodified TiO2 as a photocatalyst are the unwanted fast recombination of electron/hole pairs and the lower effectiveness in the presence of visible light irradiation. Doping a transition metal or a non-metal into TiO2 and its combination with another photocatalyst have been used to enhance its photoactivity. This study is to develop a new photocatalyst by the combination of TiO2 with another semiconductor oxide (Fe2O3) and its doping with transition metal such as Ag. Combined photocatalysts of Fe2O3 /TiO2 (with different mass ratio of Fe:TiO2) is synthesized and then silver ion is doped to combine photocatalysts (with different mass ratio of Ag:TiO2) to produce a new composite photocatalyst of Ag/TiO2/Fe2O3. A new method of UV-assisted thermal synthesis is also employed to prepare the new composite photocatalyst. Methyl orange (MO) and Congo red (CR), as model pollutants, are used to test the developed photocatalyst. In addition, nitrogen-doped titanium dioxide photocatalyst (N-TiO2) with heterojunction structures is synthesized by three different approaches including new UV-assisted thermal synthesis, annealing, and microwave techniques. The novel UV-assisted thermal synthesis has produced encouraging results as a preparation method to prepare N-TiO2 at lower temperature and atmospheric pressure as well as a lower cost. Design of Experiment (DOE) along with response surface methodology (RSM) is used to optimize the photocatalytic activity of N-TiO2 as well as the affecting parameters (wavelength, light intensity, pH, and initial TOC) for decomposition of organics. The structure of all synthesized composite photocatalysts are investigated by X-ray diffraction (XRD). Scanning electron microscopy (SEM) combined with energy-dispersive X-ray spectroscopy (EDS) is employed to evaluate surface characteristics and elemental analysis of synthesized photocatalysts. Specific surface area of photocatalysts is measured based on Brunauer, Emmett and Teller (BET) technique. Results show that bare TiO2 has the lowest photocatalytic activity in degradation of organics. When silver is doped to TiO2, the degradation of MO is slightly enhanced at specific mass ratio. The presence of Fe2O3 in the new composite causes a red shift and enhances the potential to absorb higher range of visible light. Results from XRD confirmed that Fe3+ substitutes with Ti4+ in the crystal lattice of TiO2 and crystal defect occurs. The degradation of MO in presence of Ag/TiO2/Fe2O3 (Ag/TiO2=0.005 w:w and Fe:TiO2= 0.01 w:w) reached to 95.6% under sunlight in three hours with a red shift towards visible light. It is observed that there is an optimum specific surface area of photocatalysts by doping and combining photocatalysts.

scholarly journals MECHANOCHEMICAL SYNTHESIS OF CALCIUM TITANATE AND RESEARCH OF ITS PHOTOCATALYTIC ACTIVITY

2018 ◽  
Vol 59 (6) ◽  
pp. 83 ◽  
Author(s):  
Konstantin V. Ivanov ◽  
Alexandr V. Agafonov ◽  
Olyga V. Alexeeva
Keyword(s):  
Particle Size ◽  
Photocatalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Biological Tissues ◽  
Calcium Titanate ◽  
Ceramic Technology ◽  
X Ray Diffraction ◽  
X Ray

Recently much attention is paid to the synthesis and study of the properties of inorganic materials, based on alkaline earth titanates with a perovskite structure that have various polymorphic forms depending on the temperature. Calcium titatanat (CaTiO3) can be selected from the variety of perovskites because of its relatively high dielectric constant, unique photochemical properties, chemical stability, and compatibility with biological tissues, which leads to its application in microelectronics, photocatalysis and biomedicine as bone implants. In this paper, a solid-phase synthesis of calcium titanate was carried out by ceramic technology using mechanochemistry methods. This method allows to obtain calcium titanate directly by mechanochemical activation from the initial mixture of Ca (OH)2 and TiO2, which significantly reduces the energy consumption for its production. Structural changes in the synthesized material during calcination at 120 °C, 200 °C, 400 °C, 600 °C, and 800 °C were studied. The particle size and specific surface area of powders synthesized and calcined at 800 °C was measured by laser diffraction ("Analysette 22") and the low temperature (77K) nitrogen adsorption-desorption vapor, respectively. The phase composition of the obtained materials was studied by X-ray diffraction. It was found on the basis of studies of the particle size distribution that synthesized and calcined powders contain nanoparticles with sizes of 377 and 422 nm. The samples of CaTiO3 calcined at 120 °C and 800 °C have a mesoporous structure, the specific surface area was 46 and 7 m2/g, respectively, and average pore size in powders was 4 nm. It was found by the X-ray diffraction technique that the uncalcined sample contains admixtures of CaCO3 and TiO2 that can be removed completely at 600 °C.The photocatalytic activity of the synthesized material has been studied by the example of Rhodamine B dye decoloration on the calcium titanate calcined at 800°C. It was found that the decomposition degree of dye in solution was 77% for 80 min at a 6.7% shadow adsorption.

scholarly journals Fabrication of Porous MoS2 with Controllable Morphology and Specific Surface Area for Hydrodeoxygenation

NANO ◽  
2017 ◽  
Vol 12 (09) ◽  
pp. 1750116 ◽  
Author(s):  
Zhenwi Zhang ◽  
Chuanjun Yue ◽  
Jianhen Hu
Keyword(s):  
Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Smooth Surface ◽  
High Selectivity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Large Sheet

SiO2 nanoparticles modified with aminopropyl-triethoxysilane (APTES) were used as hard templates for preparing porous MoS2. The method offers the advantages of simple steps, convenient operation, controllable pore size, and a specific surface area. Two morphologies of MoS2 were obtained by using thiourea and L-cysteine as sulfur sources, respectively. Porous MoS2 prepared by using thiourea had a smooth surface, whereas the surface of porous MoS2 prepared with L-cysteine had many burrs. The MoS2 nanomaterials with the respective morphologies were used to catalyze the hydrodeoxygenation (HDO) reaction. The activity of MoS2 prepared with L-cysteine was lower than that prepared with thiourea. Transmission electron microscopy and X-ray diffraction analyses showed that MoS2 had a large sheet-shaped structure and high crystallinity, leading to high reaction activity and high selectivity for cyclohexane. The reaction temperature also influenced the HDO significantly. The mechanism of hydrogenation of phenol was discussed.

scholarly journals Nanomaterial identification of powders: comparing volume specific surface area, X-ray diffraction and scanning electron microscopy methods

2019 ◽  
Vol 6 (1) ◽  
pp. 152-162 ◽  
Author(s):  
Claire Dazon ◽  
Olivier Witschger ◽  
Sébastien Bau ◽  
Vanessa Fierro ◽  
Philip L. Llewellyn
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
X Ray Diffraction ◽  
Reliable Criterion ◽  
X Ray ◽  
Area X ◽  
Scanning Electron

This work shows that the volume specific surface area could be a reliable criterion for nanomaterial identification.

scholarly journals Structural, photocatalytic and surface analysis of Nb/Ag codoped TiO2 mesoporous nanoparticles

2020 ◽  
Vol 96 (3) ◽  
pp. 728-741
Author(s):  
Mahtab Gorgani ◽  
Behzad Koozegar Kaleji
Keyword(s):  
Photocatalytic Activity ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Band Gap Energy ◽  
Xenon Lamp ◽  
X Ray ◽  
Mesoporous Nanoparticles

Abstract In this study, several TiO2 mesoporous nanoparticles with different mol% of niobium and silver were synthesized using the sol–gel method. The crystalline phase, chemical state, photocatalytic and optical properties, specific surface area, and morphology of mesoporous nanoparticles were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV–Vis reflective spectroscopy (UV–Vis), Brunauer–Emmett–Teller-specific surface area (BET) and field emission scanning electron microscopy (FESEM). With increasing calcination temperature, the photocatalytic activity of the samples gradually increased due to the improvement of crystallization of the anatase and rutile phases. Nb/Ag codoping sample calcined at 550 °C has reduced the band gap energy (3.17 eV to 3.06 eV) and improved the photocatalytic properties of samples under visible light (xenon lamp, 200 W for 1 h and 2 h). Doped TiO2 mesoporous nanoparticles were shown to have the highest photocatalytic activity as compared with the pure TiO2 nanoparticles. The best photocatalytic efficiency of codoped TiO2 mesoporous nanoparticles was observed for the TNA3 sample calcined under 550 °C, containing molar contents of Nb (0.5 mol%) and Ag (1 mol%) dopant ions with 95.60% efficiency.

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