scholarly journals Synthesis of C-N-S-Tridoped TiO2 from Vietnam Ilmenite Ore and Its Visible Light-Driven-Photocatalytic Activity for Tetracyline Degradation

2020 ◽  
Vol 2020 ◽  
pp. 1-14 ◽  
Author(s):  
Nguyen Thi Lan ◽  
Vo Hoang Anh ◽  
Hoang Duc An ◽  
Nguyen Phi Hung ◽  
Dao Ngoc Nhiem ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Nitrogen Adsorption ◽  
Photocatalytic Decomposition ◽  
Raman Scattering Spectroscopy ◽  
X Ray ◽  
Visible Light Driven

In this study, C-N-S-tridoped TiO2 composite was fabricated from TiO2 prepared from ilmenite ore and thiourea by means of hydrothermal method. The obtained material was characterized by X-ray diffraction, Raman scattering spectroscopy, UV-Vis diffuse reflectance spectroscopy, nitrogen adsorption-desorption isotherms, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). It was found that C-N-S-tridoped TiO2 material has a large specific surface area, showing good photocatalytic activity on the degradation of antibiotic tetracycline in visible light region. The study on the mechanism of tetracycline photodegradation using the liquid chromatography with mass spectrometry was performed. It was found that tetracycline has been degraded over C-N-S-tridoped TiO2 catalyst into many different intermediates which can eventually be converted into CO2 and H2O. The kinetics of photocatalytic decomposition of tetracycline were investigated. In addition, the obtained material could catalyze well the degradation of other antibiotics (ciprofloxacin and chloramphenicol) and dyes (rhodamine-B, methylene blue, and organe red). The catalyst was stable after five recycles with slight loss of catalytic activity, which indicates great potential for practical application of C-N-S-tridoped TiO2 catalyst in treatment of wastewater containing tetracycline in particular or antibiotics in general.

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

2020 ◽  
Vol 2020 ◽  
pp. 1-9 ◽  
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.

scholarly journals Fabrication of Bi-DopedTiO2Spheres with Ultrasonic Spray Pyrolysis and Investigation of Their Visible-Light Photocatalytic Properties

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Jianhui Huang ◽  
Wahkit Cheuk ◽  
Yifan Wu ◽  
Frank S. C. Lee ◽  
Wingkei Ho
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Spray Pyrolysis ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Ultrasonic Spray Pyrolysis ◽  
X Ray ◽  
Ultrasonic Spray ◽  
Doped Titania

Bismuth-doped TiO2submicrospheres were synthesized by ultrasonic spray pyrolysis. The prepared bismuth-doped titania was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), UV-visible diffuse reflectance spectroscopy (UV-vis DRS), and X-ray photoelectron spectroscopy (XPS). Aqueous photocatalytic activity was evaluated by the decomposition of methyl orange under visible-light irradiation. The results indicate that doping of bismuth remarkably affects the phase composition, crystal structure, and the photocatalytic activity. The sample with 2% Bi exhibits the optimum photocatalytic activity.

Improved visible-light photocatalytic activity of sodium tantalum oxide via biomass-derived silk fibroin doping

2018 ◽  
Vol 89 (7) ◽  
pp. 1332-1339
Author(s):  
Yehua Sun ◽  
Yuzhuo Luo ◽  
Yaofeng Zhu ◽  
Yaqin Fu
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Silk Fibroin ◽  
Photoelectron Spectroscopy ◽  
Structural Changes ◽  
Diffuse Reflectance Spectroscopy ◽  
Hydrothermal Process ◽  
X Ray ◽  
Transmission Electron

Biomass-derived silk fibroin (SF)-doped NaTaO3 catalysts were successfully synthesized by a simple hydrothermal process using SF as the dopant. The as-prepared samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and ultraviolet-visible diffuse reflectance spectroscopy (UV-vis DRS) analyses. The samples were tested as photocatalysts in the degradation of methylene blue under UV and visible light. XRD results showed the monoclinic structure of NaTaO3 lacking significant structural changes after anion doping. SEM and TEM images revealed the nanocubic morphology of the samples, the crystal particle sizes of which were about 100–300 nm. The XPS spectrum showed the peak of Ta4p3&N1s, indicating the combination of N and Ta. The UV-vis DRS results of the samples revealed a cut-off edge that red shifted from 315 nm of the pure NaTaO3 to 324 nm of the SF-doped counterpart. SF doping helped narrow the band gap and rendered the prepared sample sensitive to visible light. Under UV and visible-light irradiation, SF-doped NaTaO3 exhibited higher photocatalytic activity than that the undoped compound. SF-doped NaTaO3 samples also exhibited excellent stability during the recycling photocatalytic process.

scholarly journals Enhanced Visible-Light-Driven Photocatalytic Activity of ZnAl Layered Double Hydroxide by Incorporation of Co2+

2018 ◽  
Vol 13 (3) ◽  
pp. 502 ◽  
Author(s):  
Deyang Li ◽  
Lihui Fan ◽  
Min Qi ◽  
Yanming Shen ◽  
Dongbin Liu ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Layered Double Hydroxide ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Degradation Mechanism ◽  
Bet Surface Area ◽  
X Ray ◽  
Visible Light Driven ◽  
Double Hydroxide

Co-doped ZnAl layered double hydroxides (LDH) were papered by coprecipitation. The prepared samples were characterized by multiple techniques including X-ray Diffraction (XRD), Brunauer−Emmett−Teller (BET) surface area, Scanning Electronic Microscopy (SEM), Transmission Electron Microscopy (TEM), X-ray Photoelectron Spectroscopy (XPS) and UV−Vis Diffuse-Reflectance Spectroscopy (UV−Vis DRS). The incorporation of Co2+ into the ZnAl LDH sheets as CrO6 octahedron forms a new  energy level which contributes for the excitation of electrons under visible light. The doped Co2+ at a reasonable content also serves as photo-generated charges separator and improves the visible light photocatalytic activity of ZnAl LDH. A degradation mechanism based on the hydroxyl radical as the active species was proposed. Copyright © 2018 BCREC Group. All rights reservedReceived: 3rd February 2018; Revised: 8th July 2018; Accepted: 13rd July 2018How to Cite: Li, D., Fan, L., Qi, M., Shen, Y., Liu, D., Li, S. (2018). Enhanced Visible-Light-Driven Photocatalytic Activity of ZnAl Layered Double Hydroxide by Incorporation of Co2+. Bulletin of Chemical Reaction Engineering & Catalysis, 13 (3): 502-511 (doi:10.9767/bcrec.13.3.2168.502-511)Permalink/DOI: https://doi.org/10.9767/bcrec.13.3.2168.502-511 

scholarly journals Synthesis of Al-MCM-41@Ag/TiO2 Nanocomposite and Its Photocatalytic Activity for Degradation of Dibenzothiophene

2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
Xuan Nui Pham ◽  
Tuan Dat Pham ◽  
Ba Manh Nguyen ◽  
Hoa Thi Tran ◽  
Dinh Trong Pham
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
High Surface ◽  
Sol Gel ◽  
High Catalytic Activity ◽  
X Ray ◽  
Mcm 41

Mesoporous Al-MCM-41@Ag/TiO2 nanocomposites were synthesized successfully by combining the sol-gel method and hydrothermal treatment, using titanium isopropoxide (TTIP), AgNO3, and Vietnamese bentonite as precursors of Ti, Ag, and Si, respectively. The synthesized materials were well characterized by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), N2 adsorption-desorption isotherm measurements, energy dispersive X-ray spectroscopy (EDX), UV-visible diffuse reflectance spectroscopy (UV-Vis/DRS), and X-ray photoelectron spectroscopy (XPS). The photocatalytic activity was evaluated by the photodegradation of dibenzothiophene (DBT) under both UV and visible light irradiation. MCM-41@Ag/TiO2 catalyst exhibited high catalytic activity for the oxidative desulfurization (ODS) of DBT reaching almost 100% conversions at 50°C after 2 h under UV and visible light irradiations. The significant enhanced degradation of DBT over Al-MCM-41@Ag/TiO2 might be due to the synergy effects of high surface area of MCM-41, well-distributed TiO2 anatase, and reduced electron-hole recombination rates due to the dispersion of Ag nanoparticles.

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 Study on Synthesis and Photocatalytic Activity of Porous Titania Nanotubes

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
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%.

Thermally driven characteristic and highly photocatalytic activity based on N-isopropyl acrylamide/high-substituted hydroxypropyl cellulose/g-C3N4 hydrogel by electron beam pre-radiation method

2020 ◽  
pp. 089270572094421
Author(s):  
Guo Liu ◽  
Ting-Ting Li ◽  
Xiao-Fang Song ◽  
Jin-Yu Yang ◽  
Jiang-Tao Qin ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Electron Beam ◽  
Visible Light ◽  
Diffuse Reflectance Spectroscopy ◽  
Hydroxypropyl Cellulose ◽  
Resonance Spectroscopy ◽  
X Ray ◽  
Isopropyl Acrylamide ◽  
Thermally Driven

A new type of N-isopropyl acrylamide/high-substituted hydroxypropyl cellulose/graphite carbon nitride (NIPAAm/HHPC/g-C3N4) smart hydrogel-based photocatalyst with thermally driven characteristic was successfully prepared by electron beam pre-radiation polymerization and radiation cross-linking methods. The agglomeration and loss of g-C3N4 nanosheets can be avoided effectively, and ensured high photocatalytic activity under visible light, once the g-C3N4 nanosheets are uniformly dispersed into the skeleton of a thermosensitive NIPAAm/HHPC hydrogel. NIPAAm/HHPC/g-C3N4 (NHC) hydrogel was characterized by nuclear magnetic resonance spectroscopy, Fourier-transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, X-ray diffraction, X-ray photoelectron spectroscopy, and diffuse reflectance spectroscopy. The microstructure of NHC was further characterized by scanning electron microscopy, transmission electron microscopy, and Brunauer–Emmett–Teller. The adsorption–photocatalytic removal rate of rhodamine B reached 71.4% at the mass ratio of g-C3N4 of 0.8% (NHC-0.8%) hydrogel in an aqueous medium under visible light. The thermal shrinkage ratio can reach 90.6% at 60°C after 5 min and could effectively achieve the function of recycling-free in a portable photocatalytic reaction device under the optimal conditions. Possible mechanism of adsorption–photocatalysis and thermally driven recycling-free on NHC hydrogel was also obtained. These thermally driven recycling-free characteristic and highly photocatalytic properties of the hybrid hydrogel-based photocatalyst show that it can be used as a promising new material with extensive applications in wastewater treatment.

scholarly journals Preparation and Characterization of Defective TiO2. The Effect of the Reaction Environment on Titanium Vacancies Formation

Materials ◽  
2020 ◽  
Vol 13 (12) ◽  
pp. 2763
Author(s):  
Zuzanna Bielan ◽  
Szymon Dudziak ◽  
Agnieszka Sulowska ◽  
Daniel Pelczarski ◽  
Jacek Ryl ◽  
...  
Keyword(s):  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance Spectroscopy ◽  
Hydrothermal Reaction ◽  
High Photocatalytic Activity ◽  
Paramagnetic Resonance ◽  
X Ray ◽  
Light Activity ◽  
Cheap Alternative

Among various methods of improving visible light activity of titanium(IV) oxide, the formation of defects and vacancies (both oxygen and titanium) in the crystal structure of TiO2 is an easy and relatively cheap alternative to improve the photocatalytic activity. In the presented work, visible light active defective TiO2 was obtained by the hydrothermal reaction in the presence of three different oxidizing agents: HIO3, H2O2, and HNO3. Further study on the effect of used oxidant and calcination temperature on the physicochemical and photocatalytic properties of defective TiO2 was performed. Obtained nanostructures were characterized by X-ray diffractometry (XRD), specific surface area (BET) measurements, UV-Vis diffuse reflectance spectroscopy (DR-UV/Vis), photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR) spectroscopy. Degradation of phenol as a model pollutant was measured in the range of UV-Vis and Vis irradiation, demonstrating a significant increase of photocatalytic activity of defective TiO2 samples above 420 nm, comparing to non-defected TiO2. Correlation of EPR, UV-Vis, PL, and photodegradation results revealed that the optimum concentration of HIO3 to achieve high photocatalytic activity was in the range of 20–50 mol%. Above that dosage, titanium vacancies amount is too high, and the obtained materials’ photoactivity was significantly decreased. Studies on the photocatalytic mechanism using defective TiO2 have also shown that •O2− radical is mainly responsible for pollutant degradation.

scholarly journals Significantly Enhanced Aqueous Cr(VI) Removal Performance of Bi/ZnO Nanocomposites via Synergistic Effect of Adsorption and SPR-Promoted Visible Light Photoreduction

Catalysts ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 426 ◽  
Author(s):  
Xiaoya Yuan ◽  
Zijuan Feng ◽  
Jianjun Zhao ◽  
Jiawei Niu ◽  
Jiasen Liu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Synergistic Effect ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Electrochemical Impedance ◽  
Diffuse Reflectance Spectroscopy ◽  
X Ray ◽  
Enhanced Absorption ◽  
Bismuth Nanoparticles ◽  
Effective Transfer

Bismuth nanoparticles (BiNPs) and Zinc Oxide photocatalysts (BiNPs/ZnO) with different Bi loadings were successfully prepared via a facile chemical method. Their morphology and structure were thoroughly characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), UV-Vis (Ultraviolet-Visible) diffuse reflectance spectroscopy (DRS), photoluminescence spectra (PL), and electrochemical impedance spectroscopy (EIS). The results showed that a modification of hexagonal wurtzite-phase ZnO nanoparticles with Bi is achievable with an intimate interfacial interaction within its composites. The performance of the photocatalytic Cr(VI) removal under visible light irradiation indicated that BiNPs/ZnO exhibited a superior removal performance to bare ZnO, Bi, and the counterpart sample prepared using a physical mixing method. The excellent performance of the BiNPs/ZnO photocatalysts could be ascribed to the synergistic effect between the considerable physical Cr (VI) adsorption and enhanced absorption intensity in the visible light region, due to the surface plasmon resonance (SPR) as well as the effective transfer and separation of the photogenerated charge carriers at the interface.

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