Nanostructured (Sn,Ti, Nb)O2 Solid Solution for Hydrogen Sensing

2006 ◽  
Vol 915 ◽  
Author(s):  
Maria Cristina Carotta ◽  
Michele Benetti ◽  
Vincenzo Guidi ◽  
Sandro Gherardi ◽  
Cesare Malagu' ◽  
...  
Keyword(s):  
Solid Solution ◽  
Screen Printing ◽  
Single Phase ◽  
X Ray Diffraction ◽  
Molar Ratios ◽  
Hydrogen Sensing ◽  
The Mean ◽  
Co Precipitation ◽  
Screen Printing Technology ◽  
Reducing Gases

AbstractA novel co-precipitation route for preparing pure nanograined (Ti, Sn, Nb)O2 solid solution has been accomplished. The solid solution containing the three elements has been synthesized with the molar ratios for Sn:Ti:Nb 100:42:5. Electron microscopy and X-ray diffraction have been adopted to observe the morphology, the crystalline structure and the mean grain radius. Calcining at 550, 650, 850 or 1050 °C for 2h, showed rutile-like single-phase.The prepared powders have been deposited to produce gas sensors in form of thick films through screen-printing technology. SEM micrographs of both powders and films showed regularly-shaped particles with grain dimensions at nanometric level, the nanostructure being maintained up to 1050°C. The sensors have been tested with different reducing gases showing large responses to hydrogen and good selectivity.

Physical and Optical Properties of Indium Oxide: Tin Nanoparticles Synthesized by Co-Precipitation Method

2015 ◽  
Vol 659 ◽  
pp. 604-608 ◽  
Author(s):  
Jiruntanin Kanoksinwuttipong ◽  
Wisanu Pecharapa ◽  
Russameeruk Noonuruk ◽  
Wicharn Techitdheera
Keyword(s):  
Optical Properties ◽  
Single Phase ◽  
Precipitation Method ◽  
Synthesis Process ◽  
X Ray Diffraction ◽  
Optical Absorbance ◽  
Molar Ratios ◽  
Tin Nanoparticles ◽  
Ion Substitution ◽  
Co Precipitation

Indium oxide:tin nanoparticles were synthesized by co-precipitation method using InCl3 and SnCl4·5H2O as starting precursor with different molar ratios of Sn:In. The crystalline structure, optical properties, chemical bonding and morphologies of all samples were characterized by X-ray diffraction (XRD), UV–vis spectrometer, Raman spectroscopy and field emission scanning electron microscope, respectively. The XRD results show that the crystallinity of as-synthesized powders was initially amorphous phase. After calcination at 400 °C for 2 h, a single phase ITO powder with 10% (mol%) SnO2 was obtained. The particle size of each sample is approximately 20-25 nm. The color of indium oxide:tin nanopowders after heat treatment changed from white to yellow due to the substitution of oxygen vacancies in the sample. After calcination, the intensity of Raman peak significantly decreased with increasing amount of Sn loading. This phenomenon indicates that ion substitution may occur during the synthesis process. Moreover, it is noticed that the optical absorbance of obviously changed with increasing Sn loading.

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.

scholarly journals Synthesis of Ce1−xPdxO2−δ Solid Solution in Molten Nitrate

Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 640
Author(s):  
Hideaki Sasaki ◽  
Keisuke Sakamoto ◽  
Masami Mori ◽  
Tatsuaki Sakamoto
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Solid Solutions ◽  
Photoelectron Spectroscopy ◽  
Synthesis Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Co Precipitation ◽  
Ionic States

CeO2-based solid solutions in which Pd partially substitutes for Ce attract considerable attention, owing to their high catalytic performances. In this study, the solid solution (Ce1−xPdxO2−δ) with a high Pd content (x ~ 0.2) was synthesized through co-precipitation under oxidative conditions using molten nitrate, and its structure and thermal decomposition were examined. The characteristics of the solid solution, such as the change in a lattice constant, inhibition of sintering, and ionic states, were examined using X-ray diffraction (XRD), scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM−EDS), transmission electron microscopy (TEM)−EDS, and X-ray photoelectron spectroscopy (XPS). The synthesis method proposed in this study appears suitable for the easy preparation of CeO2 solid solutions with a high Pd content.

Elaboration, Structure and Mössbauer Spectroscopy of Nanostructured Fe100−xSix Powders Elaborated by Mechanical Alloying

SPIN ◽  
2017 ◽  
Vol 07 (02) ◽  
pp. 1750002 ◽  
Author(s):  
M. Hemmous ◽  
A. Guittoum
Keyword(s):  
Magnetic Field ◽  
Solid Solution ◽  
Mechanical Alloying ◽  
Hyperfine Magnetic Field ◽  
Lattice Parameter ◽  
X Ray Diffraction ◽  
X Ray ◽  
Grain Sizes ◽  
The Mean ◽  
Xrd Studies

We have studied the effect of the silicon concentration on the structural and hyperfine properties of nanostructured Fe[Formula: see text]Six powders ([Formula: see text], 20, 25 and 30[Formula: see text]at.%) prepared by mechanical alloying. The X-ray diffraction (XRD) studies indicated that after 72[Formula: see text]h of milling, the solid solution bcc-[Formula: see text]-Fe(Si) is formed. The grain sizes, [Formula: see text]D[Formula: see text] (nm), decreases with increasing Si concentration and reaches a minimum value of 11[Formula: see text]nm. We have found that the lattice parameter decreases with increasing Si concentration. The changes in values are attributed to the substitutional dissolution of Si in Fe matrix. From the adjustment of Mössbauer spectra, we have shown that the mean hyperfine magnetic field, [Formula: see text]H[Formula: see text] (T), decreases with increasing Si concentration. The substitutional dependence of [Formula: see text]H[Formula: see text] (T) can be attributed to the effect of p electrons Si influencing electrons d of Fe.

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.

Influence of Annealing Time on Microstructure of Ni-W Alloys

2013 ◽  
Vol 747-748 ◽  
pp. 613-618
Author(s):  
Qiao Zhang ◽  
Shu Hua Liang ◽  
Chen Zhang ◽  
Jun Tao Zou
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Grain Size ◽  
Grain Boundaries ◽  
Annealing Time ◽  
Single Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Average Grain Size ◽  
Scanning Electron

The as-cast Ni-W alloys with 15wt%W, 25wt%W and 30wt%W were annealed in hydrogen at 1100. The effect of the annealing time on the microstructure of Ni-W alloys was studied, and the phase constituents and microstructure of annealed Ni-W alloys were characterized by the X-ray diffraction (XRD) and scanning electron microscopy (SEM). The results showed that no any phase changed for Ni-15%W, Ni-25%W and Ni-30%W alloys annealed for 60 min, 90 min and 150 min, which were still consisted of single-phase Ni (W) solid solution. However, microstructure had a significant change after annealing. With increase of annealing time, the microstructure of Ni-15%W alloy became more uniform after annealing for 90 min, and the average grain size was 95μm, whereas the grain size of Ni-15%W alloy increased significantly after annealing for 150 min. For Ni-25%W and Ni-30%W, there was no obvious change on the grain size with increase of annealing time, and the amount of oxides at grain boundaries gradually reduced. After annealing for 150 min, the impurities at grain boundaries almost disappeared. Subsequently, the annealing at 1100 for 150 min was beneficial for the desired microstructure of Ni-25%W and Ni-30%W alloys.

Synthesis of Ti3Si0.4Al0.8C1.8 Solid Solution

2008 ◽  
Vol 368-372 ◽  
pp. 995-997
Author(s):  
Cui Wei Li ◽  
Hong Xiang Zhai ◽  
Yang Zhou ◽  
Shi Bo Li ◽  
Zhi Li Zhang
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
Single Phase ◽  
Lattice Parameters ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Powder Mixtures ◽  
X Ray ◽  
Scanning Electron

In this study, free Ti/Si/Al/C powder mixtures with molar ratio of 3:0.4:0.8:1.8 were heated in Argon with various schedules, in order to reveal the possibility for the synthesis of Ti3Si0.4Al0.8C1.8 solid solution powder. X-ray diffraction (XRD) was used for the evaluation of phase identities of the powder after different treatments. Scanning electron microscopy (SEM) was used to observe the morphology of the Ti3Si0.4Al0.8C1.8 solid solution. XRD results showed that predominantly single phase samples of Ti3Si0.4Al0.8C1.8 was prepared after heating at 1400oC for 5 min in Argon and the lattice parameters of Ti3Si0.4Al0.8C1.8 lay between those of Ti3SiC2 and Ti3AlC2.

scholarly journals Structural and magnetic properties of mechanochemically synthesized nanosized yttrium titanate

2012 ◽  
Vol 66 (3) ◽  
pp. 309-315 ◽  
Author(s):  
Tanja Barudzija ◽  
Alexey Gusev ◽  
Dragana Jugovic ◽  
Milena Marinovic-Cincovic ◽  
Miroslav Dramicanin ◽  
...  
Keyword(s):  
Quantum Interference ◽  
Single Phase ◽  
High Energy ◽  
Argon Atmosphere ◽  
Molar Ratio ◽  
Superconducting Quantum Interference Device ◽  
X Ray Diffraction ◽  
X Ray ◽  
The Mean ◽  
First Time

Nanosized perovskite YTiO3 with the mean crystallite size of 18 nm was synthesized for the first time by mechanochemical treatment. The mechanochemical solid state reaction between commercial Y2O3 powder and mechanochemically synthesized TiO powder in molar ratio 0.5:1 was completed for 3 h in a high-energy planetary ball mill in argon atmosphere. The heating in vacuum at 1150 ?C for 12 h transforms nanosized YTiO3 to a well-crystallized single-phase perovskite YTiO3. Both samples were characterized by X-ray diffraction (XRD) and thermogravimetric (TGA/DTA) analyses, as well as superconducting quantum interference device magnetometer (SQUID) measurements.

Effects of V2O5 on the synthesis of Ba2Ti9O20 powders

2005 ◽  
Vol 20 (10) ◽  
pp. 2741-2744 ◽  
Author(s):  
Huixing Lin ◽  
Wei Chen ◽  
Lan Luo
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Scanning Electron Microscopy ◽  
Single Phase ◽  
X Ray Diffraction ◽  
Eutectic Liquid ◽  
X Ray ◽  
Intermediate Phases ◽  
Phase Pure ◽  
Scanning Electron

Phase-pure Ba2Ti9O20 powders were made by doping 3 wt% of V2O5 to a Ba:Ti = 2:9 molar composition, and the effects of the dopant on the phase formation were investigated. The study shows that BaTiO3, BaTi2O5, and BaTi4O9 were the intermediate phases before the formation of Ba2Ti9O20 for samples with or without V2O5. However, with V2O5 doping, the temperature at which Ba2Ti9O20 occurred were lowered from 1150 to 1050 °C and single phase Ba2Ti9O20 powders was easily obtained at 1150 °C for 2 h. Microstructure of the powders was examined by field emission scanning electron microscopy. No evidence of V2O5–Ba2Ti9O20 solid-solution was found by x-ray diffraction and energy-dispersive spectroscopy. The benefit of V2O5 to facilitate the Ba2Ti9O20 synthesis is most probably due to a vanadium-containing eutectic liquid phase which accelerates the migration of reactant species.

On the Precipitation Behavior at 250 and 300 °C of WE54 Supersaturated Solid Solution

2012 ◽  
Vol 629 ◽  
pp. 85-89 ◽  
Author(s):  
S. Tighiouaret ◽  
H. Azzeddine ◽  
A. Sam ◽  
A. Sari ◽  
B. Alili ◽  
...  
Keyword(s):  
Solid Solution ◽  
Supersaturated Solid Solution ◽  
Precipitation Sequence ◽  
Micro Hardness ◽  
X Ray Diffraction ◽  
Precipitation Behavior ◽  
X Ray ◽  
The Mean ◽  
Kinetics Of

The current study seeks to further understand the precipitation sequence in a WE54 Mg alloy using in situ X-ray diffraction, micro-hardness and electrical resistivity during ageing at 250 and 300 °C. We show that the mean hardening effect is due to the precipitation of β' and β1metastable phases. The analysis of the kinetics of the precipitation shows that both phases nucleate at grain boundaries and within grains in the form of plates.

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