scholarly journals Influence of Molybdenum Content and MoOxy-Species on the Textural and Structural ZrO2Properties

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Alberto Hernández Zapién ◽  
Juan Manuel Hernández Enríquez ◽  
Ricardo García Alamilla ◽  
Guillermo Sandoval Robles ◽  
Ulises Páramo García ◽  
...  
Keyword(s):  
Thermal Analyses ◽  
Sol Gel ◽  
Textural Properties ◽  
Molybdenum Content ◽  
X Ray Diffraction ◽  
Surface Areas ◽  
Metal Contents ◽  
High Metal ◽  
Synthesized Materials

The present work proposes to study the incorporation of molybdenum into the zirconium oxide precursor (Zr(OH)4), in order to analyze its possible repercussions on the textural and structural zirconia properties (ZrO2). For this, the Zr(OH)4was synthesized by the sol-gel method and modified with 5, 10, and 15 wt% of molybdenum into the stabilized oxide. The synthesized materials were dried at 120°C for 24 h and then were calcined at 600°C for 3 h. The characterization of the solids was carried out by thermal analysis, X-ray diffraction, nitrogen physisorption, infrared spectroscopy, and scanning electron microscopy. The thermal analyses results showed that the change from the amorphous to the crystalline phase of ZrO2is shifted to higher temperatures due to the presence of molybdenum content. Tetragonal phase was identified for all synthesized materials, showing a decrease in crystallinity as a function of the metal content. The textural properties were improved due to the incorporation of molybdenum into the ZrO2structure, developing specific surface areas which are above up to four times the area of pure ZrO2. The synthesized materials presented spherical morphology with particle sizes less than 1 µm, with a change of this morphology for high metal contents (15 wt%) being observed.

scholarly journals REMOVAL OF NORFLOXACIN BY TiO2-SBA-15 PHOTOCATALYST

2020 ◽  
Vol 58 (3A) ◽  
pp. 13
Author(s):  
Nguyễn Thị Thu Trang ◽  
Trần Quang Vinh ◽  
Nguyễn Thành Đồng ◽  
Phạm Tuấn Linh ◽  
Nguyễn Viết Hoàng ◽  
...  
Keyword(s):  
Uv Light ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Surface Areas ◽  
Pluronic P123 ◽  
Adsorption Capacities ◽  
Transmission Electron ◽  
Photocatalytic Activities ◽  
Adsorption Desorption ◽  
Synthesized Materials

Ordered SBA-15 mesoporous silica support was synthesized by a sol-gel method using triblock copolymer Pluronic P123 and immobilized with different amounts of photocatalyst TiO2. The synthesized composites were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM) and N2 adsorption-desorption isotherms. The synthesized materials possessed specific surface areas SBET of 768 m2/g, 544 m2/g, 421 m2/g and 333 m2/g at the TiO2:SiO2 ratio of 0, 0.25, 1.0 and 5.0, respectively. The adsorption capacities and photocatalytic activities under UV light irradiation of these materials were evaluated for Norfloxacin degradation. Experimental results indicate that the highest activity was observed on the sample with TiO2:SiO2 ratio of 1.

scholarly journals Preparation and characterization of magnetite-based silica nanocomposite

2004 ◽  
pp. 121-129 ◽  
Author(s):  
Mihaela Popovici ◽  
Cecilia Savii ◽  
Daniel Niznanský ◽  
Jan Subrt ◽  
Eva Vecernikova ◽  
...  
Keyword(s):  
Thermal Analyses ◽  
Sol Gel ◽  
Nitrogen Atmosphere ◽  
Thermal Treatments ◽  
Vibrating Sample Magnetometry ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Magnetite Phase

Sol-gel method and successive thermal treatments in vacuum and nitrogen atmosphere were employed to synthesize magnetite nanoparticles isolate them with the aid of amorphous silica. Thermogravimetric and differential thermal analyses coupled with mass spectrometry, X-ray diffraction, transmission electron microscopy, M?ssbauer spectroscopy and vibrating sample magnetometry measurements were performed on the obtained nanocomposites. The effect of atmosphere on the formation of magnetite phase was remarkable.

scholarly journals Preparation and Characterization of Novel Mixed Periodic Mesoporous Organosilica Nanoparticles

Materials ◽  
2020 ◽  
Vol 13 (7) ◽  
pp. 1569
Author(s):  
Hao Li ◽  
Laurence Raehm ◽  
Clarence Charnay ◽  
Jean-Olivier Durand ◽  
Roser Pleixats
Keyword(s):  
Cetyltrimethylammonium Bromide ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Periodic Mesoporous Organosilica ◽  
X Ray ◽  
Surface Areas ◽  
Mesoporous Organosilica ◽  
Transmission Electron ◽  
Cp Mas Nmr

We report herein the preparation of mixed periodic mesoporous organosilica nanoparticles (E-Pn 75/25 and 90/10 PMO NPs) by sol-gel co-condensation of E-1,2-bis(triethoxysilyl)ethylene ((E)-BTSE or E) with previously synthesized disilylated tert-butyl 3,5-dialkoxybenzoates bearing either sulfide (precursor P1) or carbamate (precursor P2) functionalities in the linker. The syntheses were performed with cetyltrimethylammonium bromide (CTAB) as template in the presence of sodium hydroxide in water at 80 °C. The nanomaterials have been characterized by Transmission Electron Microscopy (TEM), nitrogen-sorption measurements (BET), Dynamic Light Scattering (DLS), zeta-potential, Thermogravimetric Analysis (TGA), FTIR, 13C CP MAS NMR and small angle X-ray diffraction (p-XRD). All the nanomaterials were obtained as mesoporous rodlike-shape nanoparticles. Remarkably, E-Pn 90/10 PMO NPs presented high specific surface areas ranging from 700 to 970 m2g−1, comparable or even higher than pure E PMO nanorods. Moreover, XRD analyses showed an organized porosity for E-P1 90/10 PMO NPs typical for a hexagonal 2D symmetry. The other materials showed a worm-like mesoporosity.

scholarly journals Synthesis and Characterization of Clay Polymer Nanocomposites of P(4VP-co-AAm) and Their Application for the Removal of Atrazine

Polymers ◽  
2019 ◽  
Vol 11 (4) ◽  
pp. 721 ◽  
Author(s):  
Jorge A. Ramírez-Gómez ◽  
Javier Illescas ◽  
María del Carmen Díaz-Nava ◽  
Claudia Muro-Urista ◽  
Sonia Martínez-Gallegos ◽  
...  
Keyword(s):  
Polymer Nanocomposites ◽  
Nanocomposite Materials ◽  
Synthesis And Characterization ◽  
Cross Linking ◽  
X Ray Diffraction ◽  
Numerous Species ◽  
X Ray ◽  
Different Types ◽  
Synthesized Materials

Atrazine (ATZ) is an herbicide which is applied to the soil, and its mechanism of action involves the inhibition of photosynthesis. One of its main functions is to control the appearance of weeds in crops, primarily in corn, sorghum, sugar cane, and wheat; however, it is very toxic for numerous species, including humans. Therefore, this work deals with the adsorption of ATZ from aqueous solutions using nanocomposite materials, synthesized with two different types of organo-modified clays. Those were obtained by the free radical polymerization of 4-vinylpyridine (4VP) and acrylamide (AAm) in different stoichiometric ratios, using tetrabutylphosphonium persulfate (TBPPS) as a radical initiator and N,N′-methylenebisacrylamide (BIS) as cross-linking agent. The structural, morphological, and textural characteristics of clays, copolymers, and nanocomposites were determined through different analytical and instrumental techniques, i.e., X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and thermogravimetric analysis (TGA). Adsorption kinetics experiments of ATZ were determined with the modified and synthesized materials, and the effect of the ratio between 4VP and AAm moieties on the removal capacities of the obtained nanocomposites was evaluated. Finally, from these sets of experiments, it was demonstrated that the synthesized nanocomposites with higher molar fractions of 4VP obtained the highest removal percentages of ATZ.

scholarly journals Green synthesis and characterization of hexaferrite strontium-perovskite strontium photocatalyst nanocomposites

2020 ◽  
Vol 43 (1) ◽  
pp. 26-42 ◽  
Author(s):  
Zahra Hajian Karahroudi ◽  
Kambiz Hedayati ◽  
Mojtaba Goodarzi
Keyword(s):  
Magnetic Properties ◽  
Green Synthesis ◽  
Sol Gel ◽  
Synthesis Method ◽  
Combustion Method ◽  
Lemon Juice ◽  
X Ray Diffraction ◽  
X Ray ◽  
Auto Combustion

AbstractThis study presents a preparation of SrFe12O19– SrTiO3 nanocomposite synthesis via the green auto-combustion method. At first, SrFe12O19 nanoparticles were synthesized as a core and then, SrTiO3 nanoparticles were prepared as a shell for it to manufacture SrFe12O19–SrTiO3 nanocomposite. A novel sol-gel auto-combustion green synthesis method has been used with lemon juice as a capping agent. The prepared SrFe12O19–SrTiO3 nanocomposites were characterized by using several techniques to characterize their structural, morphological and magnetic properties. The crystal structures of the nanocomposite were investigated via X-ray diffraction (XRD). The morphology of SrFe12O19– SrTiO3 nanocomposite was studied by using a scanning electron microscope (SEM). The elemental composition of the materials was analyzed by an energy-dispersive X-ray (EDX). Magnetic properties and hysteresis loop of nanopowder were characterized via vibrating sample magnetometer (VSM) in the room temperature. Fourier transform infrared spectroscopy (FTIR) spectra of the samples showed the molecular bands of nanoparticles. Also, the photocatalytic behavior of nanocomposites has been checked by the degradation of azo dyes under irradiation of ultraviolet light.

Preparation and Characterization of Zn-Containing Hydroxyapatite/TiO2 Composite Coatings on Ti Alloys

2011 ◽  
Vol 685 ◽  
pp. 367-370 ◽  
Author(s):  
Min Qi ◽  
Da Yi Yang ◽  
Jing Ying Zhang ◽  
Hong Jun Ai
Keyword(s):  
Adhesion Strength ◽  
Composite Coatings ◽  
Energy Dispersive Spectrometer ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Zn Content ◽  
Micro Arc Oxidation ◽  
Gel Technique ◽  
Bacteria Resistance

In order to improve the osteoblast growth and bacteria resistance, Zn-containing hydroxyapatite (Zn-HA) and titanium oxide (TiO2) composite coatings were prepared to improve binding between coating and Ti substrate. TiO2 film was prepared on the surface of Ti by micro-arc oxidation (MAO) and Zn-HA coating was deposited on TiO2 using sol–gel technique. Phase structure, composition and microstructure of the surface coatings were analyzed by X-ray diffraction (XRD) and Energy Dispersive Spectrometer (EDS), respectively. The adhesion strength between the coatings with different Zn content was measured by tensile testing. The results showed that there was no significant influence of Zn content on adhesion strength between coating and Ti substrate.

Characterization of SrBi2Nb2O9 Thin Films Prepared by Sol Gel Technique

1996 ◽  
Vol 459 ◽  
Author(s):  
E. Ching-Prado ◽  
W. Pérez ◽  
A. Reynés-Figueroa ◽  
R. S. Katiyar ◽  
D. Ravichandran ◽  
...  
Keyword(s):  
Thin Films ◽  
Raman Band ◽  
Sol Gel ◽  
Orthorhombic Symmetry ◽  
X Ray Diffraction ◽  
Ft Ir ◽  
Gel Technique ◽  
High Degree ◽  
First Time

ABSTRACTThin films of SrBi2Nb2O9 (SBN) with thicknesses of 0.1, 0.2, and 0.4 μ were grown by Sol-gel technique on silicon, and annealed at 650°C. The SBN films were investigated by Raman scatering for the first time. Raman spectra in some of the samples present bands around 60, 167, 196, 222, 302, 451, 560, 771, 837, and 863 cm−1, which correspond to the SBN formation. The study indicates that the films are inhomogeneous, and only in samples with thicknesses 0.4 μ the SBN material was found in some places. The prominent Raman band around 870 cm−1, which is the A1g mode of the orthorhombic symmetry, is assigned to the symmetric stretching of the NbO6 octahedrals. The frequency of this band is found to shift in different places in the same sample, as well as from sample to sample. The frequency shifts and the width of the Raman bands are discussed in term of ions in non-equilibrium positions. FT-IR spectra reveal a sharp peak at 1260 cm−1, and two broad bands around 995 and 772 cm−1. The bandwidths of the latter two bands are believed to be associated with the presence of a high degree of defects in the films. The experimental results of the SBN films are compared with those obtained in SBT (T=Ta) films. X-ray diffraction and SEM techniques are also used for the structural characterization.

The Ferroelectric and Electrical Properties of CaBi4Ti4O15 Thin Films Prepared by Sol-Gel Technology

2011 ◽  
Vol 239-242 ◽  
pp. 891-894 ◽  
Author(s):  
Tsung Fu Chien ◽  
Jen Hwan Tsai ◽  
Kai Huang Chen ◽  
Chien Min Cheng ◽  
Chia Lin Wu
Keyword(s):  
Thin Film ◽  
Thin Films ◽  
Sol Gel ◽  
Morphological Characterization ◽  
Experimental Result ◽  
X Ray Diffraction ◽  
Solution Deposition ◽  
Capacitance Voltage ◽  
Preferential Crystal Orientation

In this study, thin films of CaBi4Ti4O15with preferential crystal orientation were prepared by the chemical solution deposition (CSD) technique on a SiO2/Si substrate. The films consisted of a crystalline phase of bismuth-layer-structured dielectric. The as-deposited CaBi4Ti4O15thin films were crystallized in a conventional furnace annealing (RTA) under the temperature of 700 to 800°C for 1min. Structural and morphological characterization of the CBT thin films were investigated by X-ray diffraction (XRD) and field-emission scanning electron microscope (FE-SEM). The impedance analyzer HP4294A and HP4156C semiconductor parameters analyzer were used to measurement capacitance voltage (C-V) characteristics and leakage current density of electric field (J-E) characteristics by metal-ferroelectric-insulator- semiconductor (MFIS) structure. By the experimental result the CBT thin film in electrical field 20V, annealing temperature in 750°C the CBT thin film leaks the electric current is 1.88x10-7A/cm2and the memory window is 1.2V. In addition, we found the strongest (119) peak of as-deposited thin films as the annealed temperature of 750°C

scholarly journals A Facile Synthesis and Characterization of Highly Crystalline Submicro-Sized BiFeO3

Materials ◽  
2020 ◽  
Vol 13 (13) ◽  
pp. 3035
Author(s):  
Dovydas Karoblis ◽  
Diana Griesiute ◽  
Kestutis Mazeika ◽  
Dalis Baltrunas ◽  
Dmitry V. Karpinsky ◽  
...  
Keyword(s):  
Bismuth Ferrite ◽  
Cost Effective ◽  
Xrd Analysis ◽  
Synthetic Approach ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Dsc Measurements ◽  
Optimal Annealing Temperature ◽  
Synthesized Materials

In this study, a highly crystalline bismuth ferrite (BFO) powder was synthesized using a novel, very simple, and cost-effective synthetic approach. It was demonstrated that the optimal annealing temperature for the preparation of highly-pure BFO is 650 °C. At lower or higher temperatures, the formation of neighboring crystal phases was observed. The thermal behavior of BFO precursor gel was investigated by thermogravimetric and differential scanning calorimetry (TG-DSC) measurements. X-ray diffraction (XRD) analysis and Mössbauer spectroscopy were employed for the investigation of structural properties. Scanning electron microscopy (SEM) was used to evaluate morphological features of the synthesized materials. The obtained powders were also characterized by magnetization measurements, which showed antiferromagnetic behavior of BFO powders.

Preparation and Characterization of a Novel Flame Retardant

2008 ◽  
Vol 47-50 ◽  
pp. 294-297 ◽  
Author(s):  
Xiu Wei Jia ◽  
Min Zhi Rong ◽  
Ming Qiu Zhang
Keyword(s):  
Flame Retardant ◽  
Sol Gel ◽  
Average Molecular Weight ◽  
Regular Structure ◽  
Gel Permeation Chromatography ◽  
Helical Conformation ◽  
Infrared Spectrometry ◽  
Resonance Spectroscopy ◽  
X Ray Diffraction

A novel flame retardant polymethylsilsesquioxane (PMSQ) was successfully obtained via combination of non-hydrolytic and hydrolytic sol-gel routes. Chemical structure of the resultant PMSQ was determined by nuclear magnetic resonance spectroscopy, Fourier-transform infrared spectrometry and powder X-ray diffraction, respectively. All the measurements demonstrated that the product possessed regular structure with chain-to-chain width of 0.87nm and chain thickness of 0.40nm. Weight average molecular weight of PMSQ was measured to be 3.5×105 using gel permeation chromatography. Numerical simulations of the molecular structure suggested that PMSQ should exhibit cis-isotactic configuration and double helical conformation at undisturbed condition.

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