Sol-gel derived Nd1/3La1/3Ca1/3MnO3: Phase evolution and preparation of films and nanopowders

2007 ◽  
Vol 22 (6) ◽  
pp. 1737-1743 ◽  
Author(s):  
A. Pohl ◽  
G. Westin
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Single Phase ◽  
Sol Gel ◽  
Phase Evolution ◽  
Perovskite Oxide ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Cell Parameters ◽  
Transmission Electron

An all-alkoxide sol-gel route to the formation of Nd1/3La1/3Ca1/3MnO3thin films and powders has been developed. The microstructural evolution on heat treatment of the gel to yield the perovskite oxide was monitored by means of thermogravimetric analysis-differential scanning calorimetry, powder x-ray diffraction (XRD), Fourier transform infrared spectroscopy, and transmission electron microscopy (TEM)-energy dispersive spectroscopy (EDS). It was found that the amorphous gel consists of hydrated oxo-carbonate without organic residues, and on heating it decomposes in several steps, finally forming single-phase perovskite at 680 °C. Further heating results in only slight changes in the cell parameters and crystal growth. Films were prepared by spin coating, followed by heat treatment in air to a temperature of 800 °C, and studied by scanning electron microscopy, TEM-EDS, and XRD. Films on Al2O3were more porous, while films on Pt–TiO2–SiO2–Si were rather dense and consisted of areas with different crystal orientations.

Preparation and Property of Al87Ce3Ni8.5Mn1.5 Nanophase Amorphous Composites

2011 ◽  
Vol 412 ◽  
pp. 263-266
Author(s):  
Hong Wei Zhang ◽  
Li Li Zhang ◽  
Feng Rui Zhai ◽  
Jia Jin Tian ◽  
Can Bang Zhang
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Single Phase ◽  
Volume Fraction ◽  
Material Structure ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Different Temperatures

The higher mechanical strength of Al87Ce3Ni8.5Mn1.5 nanophase amorphous composites has been obtained with two methods. The first nanophase amorphous composites are directly produced by the single roller spin quenching technology. The method taken for the second nanophase amorphous composites is at first to obtain amorphous single-phase alloy, followed by annealed at different temperatures .The formative condition, the microstructure, the particle size, the volume fraction of α-Al phase and microhardness of nanophase amorphous composites etc have been investigated and compared by X-ray diffraction (XRD) and transmission electron microscopy (TEM) and differential scanning calorimetry (DSC). The microstructure of composites produced by the second method is higher than the former, the fabricated material structure of the system is more uniform and the process is easier to control.

scholarly journals Process for Producing Nano-Alpha-Alumina Powder

2011 ◽  
Vol 2011 ◽  
pp. 1-5 ◽  
Author(s):  
Fatemeh Mirjalili ◽  
Luqman Chuah Abdullah ◽  
Hasmaliza Mohamad ◽  
A. Fakhru'l-Razi ◽  
A. B. Dayang Radiah ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Particle Size ◽  
Sol Gel ◽  
Alumina Nanoparticles ◽  
Alumina Powder ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Transmission Electron ◽  
Stirring Time ◽  
Particle Size And Shape

This paper is trying to explore the effect of stirring time on the synthesis of nano-α-Alumina particles. In this study, alumina nanoparticles were synthesized through alkoxide route using sol-gel method, where aqueous solutions of aluminum isopropoxide and 0.5 M aluminum nitrate nanohydrate were used for preparing alumina sol. Sodium dodecylbenzen sulfonate (SDBS) was used as the surfactant stabilizing agent. The prepared solution was stirred at different times (24, 36, 48, and 60 hours) at 60°C. The Samples were, then, characterized by X-ray diffraction, thermogravimetry analysis (TGA), differential scanning calorimetry (DSC), scanning electron microscopy (SEM) and Transmission Electron Microscopy(TEM) . The introduction of different stirring times affected the particle size and shape and the degree of aggregation. By increasing the stirring time, (starting from 24 to 48 hours) the particle size decreased, but agglomeration became hard for 60 hours of stirring time. The finest particle size (20–30 nm) was obtained at 48-hour stirring time.

Synthesis and characteristics of nanocrystalline materials in Ti, B, C and N containing system

Open Physics ◽  
2011 ◽  
Vol 9 (2) ◽  
Author(s):  
Anna Biedunkiewicz ◽  
Paweł Figiel ◽  
Urszula Gabriel ◽  
Marta Sabara ◽  
Stanisław Lenart
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Ceramic Materials ◽  
Nanocrystalline Powders ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
C And N ◽  
Two Stages

AbstractIn this work, the results of investigations of manufacturing ceramic materials on the basis of Ti, B, C and N containing systems are presented. The nanocrystalline ceramics were synthesized using a non-hydrolytic sol-gel method. The process was carried out in two stages. In the first low-temperature stage the precursor was obtained. The synthesis of ceramic phases, however, was conducted in the second high-temperature stage, in an argon atmosphere. Depending on the initial composition of the mixtures, the temperature and the time, the following products were obtained: TiCx, TiCxN1−x, TiB2 and B4C.The course of the process was investigated by thermogravimetric and differential scanning calorimetry methods (TG-DSC) coupled with mass spectrometry (MS). The solid state products were identified with use of X-ray diffraction (XRD). The size of the crystallites was estimated by the Scherrer method. The structure and morphology images of nanocrystalline powders were obtained using scanning electron microscopy (SEM) and transmission electron microscopy (TEM).

Synthesis, Characterization, and Microwave Absorption Properties of SrFe12O19 Ferrites and FeNi3 Nanoplatelets Composites

2010 ◽  
Vol 148-149 ◽  
pp. 893-896 ◽  
Author(s):  
Ze Yang Zhang ◽  
Xiang Xuan Liu ◽  
You Peng Wu
Keyword(s):  
Electron Microscopy ◽  
Microwave Absorption ◽  
Composite Coatings ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Absorption Properties ◽  
Filling Fraction ◽  
Microwave Absorption Properties ◽  
Phase Reduction ◽  
Transmission Electron

M-typical SrFe12O19 ferrites and FeNi3 nanoplatelets were successfully prepared by the sol-gel method and solution phase reduction method, respectively. The crystalline and morphology of particles were studied by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and transmission electron microscopy (TEM). The composite coatings with SrFe12O19 ferrites and FeNi3 nanoplatelets in polyvinylchloride matrix were prepared. The microwave absorption properties of these coatings were investigated in 2-18GHz frequency range. The results showed that the M-typical SrFe12O19 ferrites and FeNi3 nanoplatelets were obtained and they presented irregular sheet shapes. With the increase of the coating thickness, the absorbing peak value moves to the lower frequency. The absorbing peak values of the wave increase along with the increasing of the content of FeNi3 nanoplatelets filling fraction. When 40% SrFe12O19 ferrites is doped with 20% mass fraction FeNi3 nanoplatelets to prepare composite with 1.5mm thickness, the maximum reflection loss is -24.8 dB at 7.9GHz and the -10 dB bandwidth reaches 3.2GHz.

scholarly journals Magnetic PbFe12O19-TiO2 nanocomposites and their photocatalytic performance in the removal of toxic pollutants

2018 ◽  
Vol 41 (3-4) ◽  
pp. 53-62 ◽  
Author(s):  
Behnaz Lahijani ◽  
Kambiz Hedayati ◽  
Mojtaba Goodarzi
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Performance ◽  
Sol Gel ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Gel Method ◽  
Sol Gel Method ◽  
Photocatalytic Effect ◽  
Transmission Electron ◽  
Ultraviolet Light Irradiation

Abstract In this work, the PbFe12O19 nanoparticles were prepared by the simple and optimized precipitation method with different organic surfactants and capping agents. In the next step, the TiO2 nanoparticles were synthesized using the sol-gel method. At the final step, the PbFe12O19-TiO2 nanocomposites were prepared via the sol-gel method. The effect of the precipitating agent on the morphology and particle size of the products was investigated. The prepared products were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and Fourier transform infrared spectroscopy. The results obtained by the vibrating sample magnetometer show the magnetic properties of the ferrite nanostructures. The photocatalytic effect of the PbFe12O19-TiO2 nanocomposite on the elimination of the azo dyes (acid black, acid violet and acid blue) under ultraviolet light irradiation was evaluated. The results indicate that the prepared nanocomposites have acceptable magnetic and photocatalytic performance.

Copper(I) Halide Nanoparticle-dispersed Glasses Prepared by Copper Staining

2005 ◽  
Vol 20 (9) ◽  
pp. 2480-2485 ◽  
Author(s):  
Kohei Kadono ◽  
Tatsuya Suetsugu ◽  
Takeshi Ohtani ◽  
Toshihiko Einishi ◽  
Takashi Tarumi ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Surface Region ◽  
Borosilicate Glasses ◽  
X Ray Diffraction ◽  
X Ray ◽  
Depth Profiles ◽  
Transmission Electron ◽  
Heat Treated ◽  
Glass Heat

Copper(I) chloride and bromide nanoparticle-dispersed glasses were prepared by means of a conventional copper staining. The staining was performed by the following process: copper stain was applied on the surfaces of Cl−- or Br−-ion-containing borosilicate glasses, and the glasses were heat-treated at 510 °C for various times. Typical exciton bands observed in the absorption spectra of the glasses after the heat treatment indicated that CuCl and CuBr particles were formed in the surface region of the glasses. The average sizes of the CuCl and CuBr particles in the glasses heat-treated for 48 h were estimated at 4.8 and 2.7 nm, respectively. The nanoparticles were also characterized by x-ray diffraction and transmission electron microscopy. Depth profiles of Cu and CuBr concentration in the glass heat-treated for 48 h were measured. Copper decreased in concentration monotonously with depth, reaching up to 60 μm, while the CuBr concentration had a maximum at about 25 μm in depth.

Preparation, characterization, and properties of polystyrene/Na-montmorillonite composites

2018 ◽  
Vol 32 (8) ◽  
pp. 1078-1091 ◽  
Author(s):  
Sibel Erol Dağ ◽  
Pınar Acar Bozkurt ◽  
Fatma Eroğlu ◽  
Meltem Çelik
Keyword(s):  
Electron Microscopy ◽  
Interlayer Spacing ◽  
Decomposition Temperature ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Sem Images ◽  
Specific Pore Volume ◽  
Transmission Electron ◽  
Thermal Stability Of

A series of polystyrene (PS)/unmodified Na-montmorillonite (Na-MMT) composites were prepared via in situ radical polymerization. The prepared composites were characterized using various techniques. The presence of various functional groups in the unmodified Na-MMT and PS/unmodified Na-MMT composite was confirmed by Fourier transform infrared spectroscopy. Morphology and particle size of prepared composites was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). According to the XRD and TEM results, the interlayer spacing of MMT layers was expanded. SEM images showed a spongy and porous-shaped morphology of composites. TEM revealed the Na-MMT intercalated in PS matrix. The thermal stability of PS/unmodified Na-MMT composites was significantly improved as compared to PS, which is confirmed using thermogravimetric analysis (TGA). The TGA curves indicated that the decomposition temperature of composites is higher at 24–51°C depending on the composition of the mixture than that of pure PS. The differential scanning calorimetry (DSC) results showed that the glass transition temperature of composites was higher as compared to PS. The moisture retention, water uptake, Brunauer–Emmett–Teller specific surface area, and specific pore volume of composites were also investigated. Water resistance of the composites can be greatly improved.

Structure and Optical Properties of ZnO and ZnO2 Nanoparticles

2019 ◽  
Vol 56 ◽  
pp. 49-62 ◽  
Author(s):  
Javier Eliel Morales-Mendoza ◽  
Francisco Paraguay-Delgado ◽  
J.A. Duarte Moller ◽  
Guillermo Herrera-Pérez ◽  
Nicolaza Pariona
Keyword(s):  
Heat Treatment ◽  
Band Edge Emission ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Transmission Electron ◽  
Colloidal Method ◽  
Zinc Peroxide ◽  
Average Size ◽  
Thermal Stability Of ◽  
Raman And Ir Spectroscopy

Zinc oxide (ZnO) and Zinc peroxide (ZnO2) nanoparticles were synthesized by colloidal method at low temperature. The thermal stability of ZnO2was studied by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC) and X-Ray diffraction (XRD). The crystalline structure and phase change from ZnO2to ZnO by heat treatment was studied in detail. Morphology and particle size was examined using Transmission Electron Microscopy (TEM), for as synthesized ZnO and ZnO2the shape of particles were cuasi-spherical for both materials with average size of 10±2.2 nm and 2.5±0.4 nm, respectively; The crystal size for ZnO obtained by heat treatment was 8±2.2 nm. Electron density contours show the chemical bond type ionic and covalent for ZnO and ZnO2. The vibrational properties were analyzed by Raman and IR spectroscopy. Band gap values were obtained from ultraviolet-visible (UV-Vis) absorbance spectrum. Photoluminescence (PL) spectrum for ZnO shows two emission edges located at 445 and 492 nm and in the case of ZnO2presents one edge at 364 nm originated from the band edge emission. The optical spectra present a hypsochromic shift, compared with some reported in the literature.

Preparation and Characterization of Nanocrystalline Gadolinium Oxide Powders and Films

2020 ◽  
Vol 850 ◽  
pp. 267-272 ◽  
Author(s):  
Regina Burve ◽  
Vera Serga ◽  
Aija Krūmiņa ◽  
Raimons Poplausks
Keyword(s):  
Electron Microscopy ◽  
Single Phase ◽  
Gadolinium Oxide ◽  
X Ray Diffraction ◽  
Cubic Crystal ◽  
Glass Substrates ◽  
Oxide Powders ◽  
Transmission Electron ◽  
The Mean

Due to its magnetic, electrical, absorption, and emission properties, nanoscale gadolinium oxide is widely used in various fields. In this research, nanocrystalline Gd2O3 powders and films on glass substrates have been produced by the extraction-pyrolytic method. X-ray diffraction analysis revealed the formation of single phase Gd2O3 with cubic crystal structure and the mean crystallite size from 9 to 25 nm in all produced materials. The morphology of samples has been characterized by scanning electron microscopy and transmission electron microscopy.

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