Synthesis of α-Fe2O3 nanoparticles and analyzing the effect of annealing temperature on its properties

2020 ◽  
Vol 38 (1) ◽  
pp. 116-121
Author(s):  
Bhargavi Ram Thimmiah ◽  
Gobi Nallathambi
Keyword(s):  
Size Distribution ◽  
Potassium Hydroxide ◽  
Annealing Temperature ◽  
X Ray Diffraction ◽  
Uniform Size ◽  
X Ray ◽  
The Mean ◽  
Co Precipitation ◽  
Tga Analysis ◽  
Uniform Size Distribution

Abstractα-Fe2O3 nanoparticles were synthesized via co-precipitation technique using ferric and ferrous salts and potassium hydroxide as precipitation agents. The samples were calcined at 350 °C, 550 °C and 750 °C for 3 hours. The obtained iron oxide was characterized by X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and dynamic light scattering (DLS). Crystallinity of the sample was studied by X-ray diffraction. SEM micrographs showed nonuniform size distribution of the particles forming agglomerates. TGA analysis revealed trace amount of weight loss and material stability for the samples calcined at temperatures above 500 °C. DLS results indicated that increasing of annealing temperature resulted in reduction of the particle size and more uniform size distribution. At the maximum annealing temperature of 750 °C, the mean diameter of the particles of 100 nm was observed.

Mechanical Properties of Porous Nanophase Materials Measured by Instrumental Indentation

1995 ◽  
Vol 400 ◽  
Author(s):  
H. Van Swygenhoven ◽  
W. Wagner ◽  
J. Löffler
Keyword(s):  
Mechanical Properties ◽  
Grain Size ◽  
Annealing Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Gas Condensation ◽  
Mean Grain Size ◽  
Nanophase Materials ◽  
The Mean ◽  
Instrumental Indentation

AbstractMechanical properties of nanostructured intermetallic Ni3Al synthesized by the inert-gas condensation technique are studied by means of instrumental indentation using the ICT-CSEMEX indenter. This instrument is a microindenter which continously measures load and displacement. Load-displacement curves are performed as function of grain size, consolidation- and annealing temperature. The mean grain size of the samples are studied by means of x-ray diffraction and small-angle neutron scattering.

The Determination of Crystallite Size and Size Distribution from Broadened X-Ray Diffraction Lines

1961 ◽  
Vol 5 ◽  
pp. 94-103 ◽  
Author(s):  
H. F. Quinn ◽  
P. Cherin
Keyword(s):  
Harmonic Analysis ◽  
Size Distribution ◽  
Fourier Coefficients ◽  
Distribution Functions ◽  
Composite Sample ◽  
X Ray Diffraction ◽  
X Ray ◽  
Mean Size ◽  
The Mean

AbstractMagnesium oxide crystallites having mean dimensions in the range of 25–1000 A can be prepared by controlled thermal decomposition of the carbonate.Following some earlier investigations of Birks and Friedman, we have determined the mean size and size distribution of several such MgO samples from the broadened X-ray diffraction lines which they exhibit. Contrary to the procedure of the above investigators, the harmonic analysis due to Stokes has been used to correct for instrumental broadening and values of mean-size and size-distribution functions obtained from the Fourier coefficients by the methods of Warren and Averbach.The results obtained are compared with average sizes and distributions obtained by direct examination of the samples in an electron microscope.A composite sample has been prepared by mixing known quantities of the sample previously studied. The distribution function obtained by harmonic analysis of one diffraction line of the composite sample is compared with the function calculated from the distributions of its components.Conclusions are drawn concerning the significance of the results obtained by the Warren technique: in particular, the average sizes obtained by this method are compared with those given by the approximate method used by Birks and Friedman.

scholarly journals Модификация структурно-морфологических свойств германия в многослойной нанопериодической структуре Al-=SUB=-2-=/SUB=-O-=SUB=-3-=/SUB=-/Ge с промежуточными слоями Si при отжиге

2021 ◽  
Vol 55 (10) ◽  
pp. 882
Author(s):  
М.В. Байдакова ◽  
Н.А. Берт ◽  
В.Ю. Давыдов ◽  
А.В. Ершов ◽  
А.А. Левин ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Annealing Temperature ◽  
Electron Beam Evaporation ◽  
X Ray Diffraction ◽  
Bimodal Size Distribution ◽  
X Ray ◽  
Transmission Electron ◽  
Mean Size ◽  
The Mean

Multi-layered nanosized Al2O3/Ge/Si structures manufactured by electron-beam evaporation and annealed at a temperature within the range 700−900◦C are examined using transmission electron microscopy, Raman spectroscopy and X-ray diffraction techniques. The periodic structure with a good layer planarity is confirmed to retain after heat treatment up to 900◦C. At an annealing temperature above 700◦C, nanocrystallites with a bimodal size distribution start to form within initially amorphous Ge layers, the mean size of small crystallites being determined by Ge layer thickness and annealing temperature. An essential loss of Ge from multi-layered structure after 900oC anneal and development of Ge1−x Six solid solution with x up to 0.07 in the nanocrystallites is revealed.

PREPARATION OF MnO2 NANOPARTICLES BY A SOLUTION BASED APPROACH FOR ELECTROCHEMICAL CAPACITOR

2020 ◽  
Vol 27 (08) ◽  
pp. 1950199 ◽  
Author(s):  
ANKUR SOAM ◽  
RAHUL KUMAR
Keyword(s):  
Electrochemical Capacitor ◽  
X Ray Diffraction ◽  
Uniform Size ◽  
X Ray ◽  
Supercapacitor Application ◽  
Energy Storage Application ◽  
Transmission Electron ◽  
Mno2 Nanoparticles ◽  
Scan Rate ◽  
Uniform Size Distribution

We report here the development of MnO2 nanostructure electrode for electrochemical energy storage application. MnO2 nanoparticles synthesized by a facile and efficient precipitation approach have been investigated for supercapacitor application. The structures and morphologies of MnO2 nanoparticles were systematically studied using X-ray diffraction, Raman spectroscopy and transmission electron microscopy. The synthesized nanoparticles are observed spherical in shape with uniform size distribution. The electrochemical properties were studied in two-electrode configuration by cyclic voltammetry process. A specific capacitance of 52.8[Formula: see text]F/g has been obtained for MnO2 nanoparticles at scan rate of 100[Formula: see text]mV/s. The electrode is able to deliver a power density of 0.66[Formula: see text]kW/kg and energy density of 1.8[Formula: see text]Wh/kg.

Effect of Reactive-Al2O3 Addition on the Pore Size Distribution and Thermal Conductivity of Carbon Blocks for Blast Furnace

2010 ◽  
Vol 97-101 ◽  
pp. 453-456 ◽  
Author(s):  
Xi Lai Chen ◽  
Ya Wei Li ◽  
Yuan Bing Li ◽  
Shao Bai Sang ◽  
Lei Zhao
Keyword(s):  
Thermal Conductivity ◽  
Blast Furnace ◽  
Pore Size Distribution ◽  
Pore Size ◽  
Size Distribution ◽  
Mercury Porosimetry ◽  
X Ray Diffraction ◽  
X Ray ◽  
Sic Whiskers ◽  
The Mean

The effect of reactive-Al2O3 addition on the pore size distribution and thermal conductivity of carbon blocks for blast furnace was investigated by using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy-dispersive X-ray, mercury porosimetry, and a laser thermal conductivity meter. The results showed that the pore size distribution and the thermal conductivity of carbon block were mainly influenced by SiC whiskers and reactive-Al2O3. With increasing addition of reactive-Al2O3, the mean pore diameter reduced and < 1μm pore volume increased of open pores owing to the more efficient filling of pores by SiC and reactive-Al2O3, and the thermal conductivities of samples increased due to the facts that the higher thermal conductivity of reactive-Al2O3 than that of brown corundum and the more formation amount of high thermal conductivity of SiC.

Isomorphous replacement in electron diffraction of wet crystals of rat hemoglobin

1983 ◽  
Vol 41 ◽  
pp. 446-447
Author(s):  
William F. Tivol ◽  
Murray Vernon King ◽  
D. F. Parsons
Keyword(s):  
Electron Diffraction ◽  
Heavy Atom ◽  
Isomorphous Substitution ◽  
X Ray Diffraction ◽  
Salt Solutions ◽  
X Ray ◽  
Isomorphous Replacement ◽  
Structure Factors ◽  
Diffraction Structure ◽  
The Mean

Feasibility of isomorphous substitution in electron diffraction is supported by a calculation of the mean alteration of the electron-diffraction structure factors for hemoglobin crystals caused by substituting two mercury atoms per molecule, following Green, Ingram & Perutz, but with allowance for the proportionality of f to Z3/4 for electron diffraction. This yields a mean net change in F of 12.5%, as contrasted with 22.8% for x-ray diffraction.Use of the hydration chamber in electron diffraction opens prospects for examining many proteins that yield only very thin crystals not suitable for x-ray diffraction. Examination in the wet state avoids treatments that could cause translocation of the heavy-atom labels or distortion of the crystal. Combined with low-fluence techniques, it enables study of the protein in a state as close to native as possible.We have undertaken a study of crystals of rat hemoglobin by electron diffraction in the wet state. Rat hemoglobin offers a certain advantage for hydration-chamber work over other hemoglobins in that it can be crystallized from distilled water instead of salt solutions.

scholarly journals Photoluminescent Properties of Hydroxyapatite and Hydroxyapatite/Multi-Walled Carbon Nanotube Composites

Crystals ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 832
Author(s):  
Edna X. Figueroa-Rosales ◽  
Javier Martínez-Juárez ◽  
Esmeralda García-Díaz ◽  
Daniel Hernández-Cruz ◽  
Sergio A. Sabinas-Hernández ◽  
...  
Keyword(s):  
Carbon Nanotube ◽  
Hexagonal Phase ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Multi Walled Carbon Nanotube ◽  
Nanotube Composites ◽  
Carbon Nanotube Composites ◽  
Co Precipitation ◽  
Functionalized Mwcnts

Hydroxyapatite (HAp) and hydroxyapatite/multi-walled carbon nanotube (MWCNT) composites were obtained by the co-precipitation method, followed by ultrasound-assisted and microwave radiation and thermal treatment at 250 °C. X-ray diffraction (XRD) confirmed the presence of a hexagonal phase in all the samples, while Fourier-transform infrared (FTIR) spectroscopy elucidated the interaction between HAp and MWCNTs. The photoluminescent technique revealed that HAp and the composite with non-functionalized MWCNTs present a blue luminescence, while the composite with functionalized MWCNTs, under UV-vis radiation shows an intense white emission. These findings allowed presentation of a proposal for the use of HAp and HAp with functionalized MWCNTs as potential materials for optoelectronic and medical applications.

scholarly journals Preparation of high-entropy carbides by different sintering techniques

2021 ◽  
Vol 56 (19) ◽  
pp. 11237-11247 ◽  
Author(s):  
Johannes Pötschke ◽  
Manisha Dahal ◽  
Mathias Herrmann ◽  
Anne Vornberger ◽  
Björn Matthey ◽  
...  
Keyword(s):  
Grain Size ◽  
Single Phase ◽  
X Ray Diffraction ◽  
Vacuum Sintering ◽  
X Ray ◽  
High Entropy ◽  
Mean Grain Size ◽  
The Mean ◽  
Gas Pressure Sintering ◽  
Hardness Values

AbstractDense (Hf, Ta, Nb, Ti, V)C- and (Ta, Nb, Ti, V, W)C-based high-entropy carbides (HEC) were produced by three different sintering techniques: gas pressure sintering/sinter–HIP at 1900 °C and 100 bar Ar, vacuum sintering at 2250 °C and 0.001 bar as well as SPS/FAST at 2000 °C and 60 MPa pressure. The relative density varied from 97.9 to 100%, with SPS producing 100% dense samples with both compositions. Grain size measurements showed that the substitution of Hf with W leads to an increase in the mean grain size of 5–10 times the size of the (Hf, Ta, Nb, Ti, V,)C samples. Vacuum-sintered samples showed uniform grain size distribution regardless of composition. EDS mapping revealed the formation of a solid solution with no intermetallic phases or element clustering. X-ray diffraction analysis showed the structure of mostly single-phase cubic high-entropy carbides. Hardness measurements revealed that (Hf, Ta, Nb, Ti, V)C samples possess higher hardness values than (Ta, Nb, Ti, V, W)C samples.

Dalnegroite, Tl5–xPb2x(As,Sb)2l–xS34, a new thallium sulphosalt from Lengenbach quarry, Binntal, Switzerland

2009 ◽  
Vol 73 (6) ◽  
pp. 1027-1032 ◽  
Author(s):  
F. Nestola ◽  
A. Guastoni ◽  
L. Bindi ◽  
L. Secco
Keyword(s):  
Polarized Light ◽  
New Mineral ◽  
X Ray Diffraction ◽  
X Ray ◽  
Elemental Concentrations ◽  
Reflected Light ◽  
Mohs Hardness ◽  
The Mean ◽  
The University ◽  
Probable Space

AbstractDalnegroite, ideally Tl4Pb2(As12Sb8)Σ20S34, is a new mineral from Lengenbach, Binntal, Switzerland. It occurs as anhedral to subhedral grains up to 200 μm across, closely associated with realgar, pyrite, Sb-rich seligmanite in a gangue of dolomite. Dalnegroite is opaque with a submetallic lustre and shows a brownish-red streak. It is brittle; the Vickers hardness (VHN25) is 87 kg mm-2(range: 69—101) (Mohs hardness ∼3—3½). In reflected light, dalnegroite is highly bireflectant and weakly pleochroic, from white to a slightly greenish-grey. In cross-polarized light, it is highly anisotropic with bluish to green rotation tints and red internal reflections.According to chemical and X-ray diffraction data, dalnegroite appears to be isotypic with chabournéite, Tl5-xPb2x(Sb,As)21-xS34. It is triclinic, probable space groupP1, witha= 16.217(7) Å,b= 42.544(9) Å,c= 8.557(4) Å, α = 95.72(4)°, β = 90.25(4)°, γ = 96.78(4)°,V= 5832(4) Å3,Z= 4.The nine strongest powder-diffraction lines [d(Å) (I/I0) (hkl)] are: 3.927 (100) (10 0); 3.775 (45) (22); 3.685 (45) (60); 3.620 (50) (440); 3.124 (50) (2); 2.929 (60) (42); 2.850 (70) (42); 2.579 (45) (02); 2.097 (60) (024). The mean of 11 electron microprobe analyses gave elemental concentrations as follows: Pb 10.09(1) wt.%, Tl 20.36(1), Sb 23.95(1), As 21.33(8), S 26.16(8), totalling 101.95 wt.%, corresponding to Tl4.15Pb2.03(As11.86Sb8.20)S34. The new mineral is named for Alberto Dal Negro, Professor in Mineralogy and Crystallography at the University of Padova since 1976.

scholarly journals A Study of Thin Film Resistors Prepared Using Ni-Cr-Si-Al-Ta High Entropy Alloy

2015 ◽  
Vol 2015 ◽  
pp. 1-7 ◽  
Author(s):  
Ruei-Cheng Lin ◽  
Tai-Kuang Lee ◽  
Der-Ho Wu ◽  
Ying-Chieh Lee
Keyword(s):  
Annealing Temperature ◽  
Phase Evolution ◽  
Amorphous Structure ◽  
High Entropy Alloy ◽  
X Ray Diffraction ◽  
Temperature Coefficient Of Resistance ◽  
X Ray ◽  
High Entropy ◽  
Transmission Electron ◽  
Thin Film Resistors

Ni-Cr-Si-Al-Ta resistive thin films were prepared on glass and Al2O3substrates by DC magnetron cosputtering from targets of Ni0.35-Cr0.25-Si0.2-Al0.2casting alloy and Ta metal. Electrical properties and microstructures of Ni-Cr-Si-Al-Ta films under different sputtering powers and annealing temperatures were investigated. The phase evolution, microstructure, and composition of Ni-Cr-Si-Al-Ta films were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and Auger electron spectroscopy (AES). When the annealing temperature was set to 300°C, the Ni-Cr-Si-Al-Ta films with an amorphous structure were observed. When the annealing temperature was at 500°C, the Ni-Cr-Si-Al-Ta films crystallized into Al0.9Ni4.22, Cr2Ta, and Ta5Si3phases. The Ni-Cr-Si-Al-Ta films deposited at 100 W and annealed at 300°C which exhibited the higher resistivity 2215 μΩ-cm with −10 ppm/°C of temperature coefficient of resistance (TCR).

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