scholarly journals Comparison of the structural and photo-catalytic properties of nanostructured Fe3O4/TiO2 core-shell composites synthesized by ultrasonic and Stöber methods

2020 ◽  
Vol 52 (4) ◽  
pp. 415-432
Author(s):  
Faezeh Parast ◽  
Mehdi Montazeri-Pour ◽  
Masoud Rajabi ◽  
Fatemeh Bavarsiha
Keyword(s):  
Electron Microscopy ◽  
Methylene Blue ◽  
Catalytic Properties ◽  
Uv Light ◽  
Oxide Coating ◽  
Blue Dye ◽  
Core Shell ◽  
Methylene Blue Dye ◽  
X Ray ◽  
Titanium Oxide Coating

In the present research, Fe3O4/TiO2 magnetic photo-catalytic nanocomposites with a core/shell structure were successfully synthesized using two techniques of ultrasonic and St?ber. In this way, iron oxide (II, III) nanoparticles as soft magnetic cores of this composite were prepared by utilizing a chemical method assisted by ultrasound with a Fe+3/Fe+2 molar ratio of 1.5 under the nitrogen atmosphere. Thereafter, titanium oxide coating was performed on Fe3O4 nanoparticles by using tetrabutyl orthotitanate (TBOT) and titanium isopropoxide (TTIP) precursors. The resultant nanostructures were characterized by means of X-ray powder diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, energy dispersive X-ray (EDX) analysis, vibrating sample magnetometer (VSM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Through findings obtained from TEM examinations, the formation of core/shell nanostructure was confirmed in the prepared Fe3O4/TiO2 composites. Analysis of magnetic properties revealed that titanium oxide coating on iron oxide nanoparticles reduces saturation magnetization (Ms). The values of saturation magnetization for Fe3O4 powder and Fe3O4/TiO2 nanocomposite powders achieved via ultrasonic and St?ber methods were 60, 23 and 9 emu/g, respectively. Photo-catalytic properties of Fe3O4/TiO2 nanostructures were evaluated by the use of methylene blue dye under UV light. Results indicated that Fe3O4/TiO2 composite obtained by the St?ber method has a better photo-catalytic property as well as a decreased but acceptable magnetic separation. Degradation of methylene blue dye in the presence of photo-catalytic powder prepared by ultrasonic and St?ber procedures was 61 and 69 %, respectively, within 90 minutes of UV light exposure.

scholarly journals Degradation of Methylene Blue Dye in the Presence of Visible Light Using SiO2@α-Fe2O3 Nanocomposites Deposited on SnS2 Flowers

2018 ◽  
Author(s):  
Sridharan Balu ◽  
Kasimayan Uma ◽  
Guan-Ting Pan ◽  
Thomas C.-K. Yang ◽  
Sayee Kannan Ramaraj
Keyword(s):  
Methylene Blue ◽  
Three Dimensional ◽  
Semiconductor Materials ◽  
Blue Dye ◽  
Core Shell ◽  
Methylene Blue Dye ◽  
X Ray Diffraction ◽  
Facile Hydrothermal Method ◽  
X Ray ◽  
Scanning Electron

Semiconductor materials have been shown to have better photocatalytic behavior and can be utilized for the photodegradation of organic pollutants. In this work, three-dimensional flower-like SnS2 were synthesized by a facile hydrothermal method. Core-shell structured SiO2@α-Fe2O3 nanocomposites were then deposited on the top of the SnS2 flowers. The as-synthesized nanocomposites were characterized by X-ray diffraction (XRD), Raman spectroscopy, field emission scanning electron microscopy (FE-SEM), Brunauer-Emmett-Teller (BET) and photoluminescence spectroscopy (PL). The photocatalytic behavior of the SnS2-SiO2@α-Fe2O3 nanocomposites was observed by observing the degradation of methylene blue (MB). The results show an effective enhancement of photocatalytic activity for the degradation of MB especially for the 15 wt. % SiO2@α-Fe2O3 nanocomposites on SnS2 flowers.

Synthesis of TiO2 Nanoparticles Using Acinetobacter baumanii for Photocatalytic Application

2020 ◽  
Vol 979 ◽  
pp. 175-179
Author(s):  
M. Nagalakshmi ◽  
N. Anusuya ◽  
S. Karuppuchamy
Keyword(s):  
Methylene Blue ◽  
Titanium Dioxide ◽  
Uv Light ◽  
Blue Dye ◽  
Biological Method ◽  
Methylene Blue Dye ◽  
Acinetobacter Baumanii ◽  
Uv Light Irradiation ◽  
Photocatalytic Application ◽  
Vis Spectroscopy

Titanium dioxide (TiO2) nanoparticles have been successfully prepared by biological method and the resulting material was characterized by XRD, FTIR, SEM, EDAX and UV-Vis spectroscopy. The synthesized TiO2 materials successfully degraded the methylene blue dye (MB) under UV light irradiation.

scholarly journals Combining the Photocatalysis and Absorption Properties of Core-Shell Cu-BTC@TiO2 Microspheres: Highly Efficient Desulfurization of Thiophenic Compounds from Fuel

Materials ◽  
2018 ◽  
Vol 11 (11) ◽  
pp. 2209 ◽  
Author(s):  
Jing Liu ◽  
Xiao-Min Li ◽  
Jing He ◽  
Lu-Ying Wang ◽  
Jian-Du Lei
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Photocatalytic Oxidation ◽  
Uv Light ◽  
Sulfur Removal ◽  
Oxidation Products ◽  
Core Shell ◽  
Adsorptive Desulfurization ◽  
X Ray ◽  
Tio2 Microspheres

A core-shell Cu-benzene-1,3,5-tricarboxylic acid (Cu-BTC)@TiO2 was successfully synthesized for photocatalysis-assisted adsorptive desulfurization to improve adsorptive desulfurization (ADS) performance. Under ultraviolet (UV) light irradiation, the TiO2 shell on the surface of Cu-BTC achieved photocatalytic oxidation of thiophenic S-compounds, and the Cu-BTC core adsorbed the oxidation products (sulfoxides and sulfones). The photocatalyst and adsorbent were combined using a distinct core-shell structure. The morphology and structure of the fabricated Cu-BTC@TiO2 microspheres were verified by scanning electron microscopy, high-resolution transmission electron microscopy, energy-dispersive x-ray spectroscopy, X-ray powder diffraction, nitrogen adsorption-desorption and X-ray photoelectron spectroscopy analyses. A potential formation mechanism of Cu-BTC@TiO2 is proposed based on complementary experiments. The sulfur removal efficiency of the microspheres was evaluated by selective adsorption of benzothiophene (BT) and dibenzothiophene (DBT) from a model fuel with a sulfur concentration of 1000 ppmw. Within a reaction time of 20 min, the BT and DBT conversion reached 86% and 95%, respectively, and achieved ADS capacities of 63.76 and 59.39 mg/g, respectively. The BT conversion and DBT conversion obtained using Cu-BTC@TiO2 was 6.5 and 4.6 times higher, respectively, than that obtained using Cu-BTC. A desulfurization mechanism was proposed, the interaction between thiophenic sulfur compounds and Cu-BTC@TiO2 microspheres was discussed, and the kinetic behavior was analyzed.

Synthesis and Characterization of SiO2@Y2MoO6:Eu3+ Core–Shell Structured Spherical Phosphors by Sol–Gel Process

2016 ◽  
Vol 16 (4) ◽  
pp. 3914-3920 ◽  
Author(s):  
G. Z Li ◽  
F. H Liu ◽  
Z. S Chu ◽  
D. M Wu ◽  
L. B Yang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Annealing Temperature ◽  
Uv Light ◽  
Sol Gel ◽  
Spherical Shape ◽  
Core Shell ◽  
X Ray ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Average Size

SiO2@Y2MoO6:Eu3+ core–shell phosphors were prepared by the sol–gel process. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectra (EDS), transmission electron microscopy (TEM), photoluminescence (PL) spectra as well as kinetic decays were used to characterize the resulting SiO2@Y2MoO6:Eu3+ core–shell phosphors. The XRD results demonstrated that the Y2MoO6:Eu3+ layers on the SiO2 spheres crystallized after being annealed at 700 °C and the crystallinity increased with raising the annealing temperature. The obtained core–shell phosphors have spherical shape with narrow size distribution (average size ca. 640 nm), non-agglomeration, and smooth surface. The thickness of the Y2MoO6:Eu3+ shells on the SiO2 cores could be easily tailored by varying the number of deposition cycles (70 nm for four deposition cycles). The Eu3+ shows a strong PL emission (dominated by 5D0–7F2 red emission at 614 nm) under the excitation of 347 nm UV light. The PL intensity of Eu3+ increases with increasing the annealing temperature and the number of coating cycles.

scholarly journals Synthesis, Characterization, and Photocatalytic Performance of Mesoporous α-Mn2O3 Microspheres Prepared via a Precipitation Route

2016 ◽  
Vol 2016 ◽  
pp. 1-7 ◽  
Author(s):  
Manoj Pudukudy ◽  
Zahira Yaakob
Keyword(s):  
Electron Microscopy ◽  
Uv Light ◽  
Thermal Transformation ◽  
Xrd Analysis ◽  
Structural Deformation ◽  
Blue Dye ◽  
X Ray Diffraction ◽  
Electron Microscopic ◽  
X Ray ◽  
Transmission Electron

α-Mn2O3 microspheres with high phase purity, crystallinity, and surface area were synthesized by the thermal decomposition of precipitated MnCO3 microspheres without the use of any structure directing agents and tedious reaction conditions. The prepared Mn2O3 microspheres were characterized by Fourier transform infrared (FTIR) spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), and Brunauer-Emmett-Teller (BET) and photoluminescence (PL) studies. The complete thermal transformation of MnCO3 to Mn2O3 was clearly shown by the FTIR and XRD analysis. The electron microscopic images clearly confirmed the microsphere-like morphology of the products with some structural deformation for the calcined Mn2O3 sample. The mesoporous texture generated from the interaggregation of subnanoparticles in the microstructures is visibly evident from the TEM and BET studies. Moreover, the Mn2O3 microstructures showed a moderate photocatalytic activity for the degradation of methylene blue dye pollutant under UV light irradiation, using air as the potential oxidizing agent.

scholarly journals Curd Mediated Facile Synthesis of ZnO/Ag/NiO Heterostructures and Visible Light Assisted Photodegradation of Methylene Blue

2020 ◽  
Vol 32 (12) ◽  
pp. 3203-3208
Author(s):  
J.P. Shubha ◽  
B.S. Prathibha ◽  
N. Jayalakshmi
Keyword(s):  
Electron Microscopy ◽  
Methylene Blue ◽  
Visible Light ◽  
Analytical Techniques ◽  
Zinc Nitrate ◽  
Blue Dye ◽  
Methylene Blue Dye ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Light Concentration

Green fuel perished curd was used to synthesize ZnO/Ag/NiO ternary heterostructure with zinc nitrate, nickel carbonate and silver nitrate as oxidizers. The obtained nanostructure was characterized by various analytical techniques such as powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (FESEM), transmission electron microscopy (TEM). The particles and flakes composition of ZnO/Ag/NiO nanomaterials was confirmed. Photocatalytic activity of ZnO/Ag/NiO was evaluated with methylene blue dye by source of light, concentration of hydrogen ion, catalyst and dye concentrations. The obtained ZnO/Ag/NiO nanoparticles reveal better catalytic property for the photodegradation of methylene blue dye under visible light.

Photocatalytic Degradation of Methylene Blue Dye over Copper(II) Complex Nanoparticle Catalyst.

2021 ◽  
pp. 138-142
Author(s):  
Hassan Wafi Garba ◽  
Abubakar Garba Ashiru ◽  
Rooshan Watanpal ◽  
Mohammed Bello ◽  
Kasimu Abubakar ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Single Phase ◽  
Uv Light ◽  
Blue Dye ◽  
Spectroscopic Techniques ◽  
Methylene Blue Dye ◽  
Ft Ir ◽  
Ir Spectroscopic ◽  
Physicochemical And Structural Properties ◽  
Nanoparticle Catalyst

Abstract—A novel copper(II) complex nanoparticles catalyst was synthesized via precipitation and calcination. The catalyst was applied for the degradation of methylene blue under UV light irradiation. The catalyst was characterized for its physicochemical and structural properties by XRD, SEM, TEM and FT-IR spectroscopic techniques. XRD studies revealed that the particles were monoclinic single phase crystalline structure, the morphology of the nanostructure was confirmed by SEM while the TEM studies revealed that the particles were FCC. FTIR spectra showed the presence of diverse vibrational functional groups. Photolysis of the methylene blue dye indicates no degradation after 1 hour reaction, while the addition of the copper(II) complex nanoparticles catalyst resulted in the decolouration of the dye by ~94%. The efficiency of the catalyst was attributed to the nanoparticle’s morphology.

Decolorization of Methylene Blue by Photocatalyst in the Ag3PO4-AgI System

2014 ◽  
Vol 970 ◽  
pp. 29-32 ◽  
Author(s):  
Pongsaton Amornpitoksuk ◽  
Sumetha Suwanboon
Keyword(s):  
Methylene Blue ◽  
Mixed Phase ◽  
Photocatalytic Properties ◽  
Precipitation Method ◽  
Blue Dye ◽  
Methylene Blue Dye ◽  
X Ray Diffraction ◽  
X Ray ◽  
Diffraction Patterns ◽  
Co Precipitation

The co-effect of PO43- and I- on the formation of a heterosturucture photocatalyst in the Ag3PO4-AgI system was studied by the co-precipitation method between AgNO3 and the precipitating agent. The precipitating agent was prepared by varying the mole ratios between Na2HPO4 and KI. At 10 mol.% KI, the product showed the mixed phase between Ag3PO4 and un-identified phase. For 30 - 90 mol.% KI, the un-identified phase and AgI were detected in the x-ray diffraction patterns. The un-identified phase strongly adsorbed the methylene blue dye. The product prepared from 30 mol.% KI had the highest content of un-identified phase and also showed the highest degree of decolorization in the dark. The photocatalytic properties of products in this system were confirmed by the decolorization of methylene blue under visible illumination.

scholarly journals Synthesis and Characterization of CeO2-SiO2Nanoparticles by Microwave-Assisted Irradiation Method for Photocatalytic Oxidation of Methylene Blue Dye

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
R. M. Mohamed ◽  
E. S. Aazam
Keyword(s):  
Methylene Blue ◽  
Photocatalytic Activity ◽  
Photocatalytic Oxidation ◽  
Uv Light ◽  
Irradiation Time ◽  
High Surface ◽  
Blue Dye ◽  
Methylene Blue Dye ◽  
Microwave Assisted ◽  
Small Pore

CeO2-SiO2nanoparticles were synthesized for the first time by a facile microwave-assisted irradiation process. The effect of irradiation time of microwave was studied. The materials were characterized by N2adsorption, XRD, UV-vis/DR, and TEM. All solids showed mesoporous textures with high surface areas, relatively small pore size diameters, and large pore volume. The X-ray diffraction results indicated that the as-synthesized nanoparticles exhibited cubic CeO2without impurities and amorphous silica. The transmission electron microscopy (TEM) images revealed that the particle size of CeO2-SiO2nanoparticles, which were prepared by microwave method for 30 min irradiation times, was around 8 nm. The photocatalytic activities were evaluated by the decomposition of methylene blue dye under UV light irradiations. The results showed that the irradiation under the microwave produced CeO2-SiO2nanoparticles, which have the best crystallinity under a shorter irradiation time. This indicates that the introduction of the microwave really can save energy and time with faster kinetics of crystallization. The sample prepared by 30 min microwave irradiation time exhibited the highest photocatalytic activity. The photocatalytic activity of CeO2-SiO2nanoparticles, which were prepared by 30 min irradiation times was found to have better performance than commercial reference P25.

scholarly journals Synthesis of bimetallic nanoparticles loaded on to PNIPAM hybrid microgel and their catalytic activity

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Mohib Ullah Kakar ◽  
Khakemin Khan ◽  
Muhammad Akram ◽  
Rokayya Sami ◽  
Ebtihal Khojah ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Methylene Blue ◽  
Metallic Nanoparticles ◽  
Bimetallic Nanoparticles ◽  
Catalytic Properties ◽  
Thiol Group ◽  
Pseudo First Order Reaction ◽  
Efficient Catalyst ◽  
Nitrogenous Compounds ◽  
X Ray

AbstractThis study was designed to preparecarboxyl-functionalized poly (N-isopropylacrylamide) PNIPAM microgels having excellent catalytic properties.Recently, researchers are trying to fabricate cost effective and efficient hybrid catalytic materials for the synthesis of nitrogenous compounds along with enhanced optical properties. For the same motive, synthesis of carboxyl-functionalized PNIPAM microgels was performed by using polymerization of soap-free emulsion of N-isopropyl acrylamide, which is NIPAM along with acrylic acid (AA). The thiol group was introduced through the imide bond mediated by carbodiimide, between carboxyl-functionalized microgels through carboxyl group and aminoethanethiol (AET). Copper, Palladium and Cu/Pd nanoparticles were incorporated successfully into thiol-functionalized PNIPAM microgels through metals thiol linkage. The synthesized microgels and hybrid encompassing metallic nanoparticles were characterized in detail by using Transmission electron microscopy (TEM), Scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron (XPS) and Fourier transformed infrared spectroscopy for structural interpretation. The thermal properties of the pure and hybrid microgels were inspected by TG analysis. The prepared nanocomposites PNIPAM-Cu, PNIPAM-Pd and PNIPAM-Cu/Pd exhibited decent catalytic properties for the degradation of 4-Nitrophenol and methylene blue, but the bimetallic Cu/Pd have remarkable catalytic properties. The catalytic reaction followed pseudo-first-order reaction with rate constants 0.223 min−1, 0.173 min−1 for 4-Nitrophenol and methylene blue in that order. In this study,we were able to establish that Cu/Pd hybrid is an efficient catalyst for 4-Nitrophenol and methylene blue as compared to its atomic analogue.

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