scholarly journals Nanocrystalline composites in TiO2 and SnO2 system for ammonia resistance sensors

2018 ◽  
Vol 12 (3) ◽  
pp. 240-247
Author(s):  
Anna Szczygielska ◽  
Zbigniew Pędzich ◽  
Wojciech Maziarz
Keyword(s):  
Phase Composition ◽  
Sol Gel ◽  
Temperature Treatment ◽  
High Temperature Treatment ◽  
Medium Size ◽  
X Ray Diffraction ◽  
Nanocrystalline Tio2 ◽  
Tio2 Anatase ◽  
Transmission Electron ◽  
Sorption Method

This work describes the production of nanocrystalline TiO2 and SnO2 oxides, as well as their nanocomposites (containing 26.9, 58.7 and 79.0wt.% of SnO2) with two-stage sol-gel method combined with high temperature treatment. The phase composition and medium size crystallites were determined using X-ray diffraction analysis (XRD) and revealed that the nanocomposites crystallize in tetragonal structures of TiO2 - anatase and SnO2 - cassiterite. Specific surface area of the nanopowders, measured using sorption method (BET), changed from 42.1 to 160.8m2/g. The morphology of the nanopowders was observed using transmission electron microscope (TEM). As indicated by TEM images, the manufactured nanopowders were well crystallized and consisted of small, spherical grains. The obtained nanopowders were also tested for NH3 gas detection application. The presented method of nanopowders synthesis enables to obtain nanocrystalline TiO2 and SnO2 oxides, as well as composites from TiO2-SnO2 of known and controlled chemical and phase composition. It also enables to obtain composites used for gas sensors. The sensor made of composite containing 58.7wt.% of SnO2 exhibited the best NH3 sensing features.

Fabrication of TiO2-Aerogel with NiB Nano-Clusters and Its Structural Characterization and Catalysis Evaluation

2006 ◽  
Vol 11-12 ◽  
pp. 7-10
Author(s):  
T. Nishi ◽  
Sakae Tanemura ◽  
Lei Miao ◽  
Masaki Tanemura ◽  
K. Suzuki
Keyword(s):  
Anatase Phase ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
Ground Sample ◽  
Tio2 Anatase ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Infrared Spectrophotometer ◽  
Ft Ir ◽  
The Difference

We have prepared titania aerogel (=AG) embedded by NiB nano-clusters by sol-gel method, immersion of the prepared wet gel into the NiB dispersed solution, and the subsequent super critical drying (=SCD). The AG was characterized by X-ray diffraction (XRD), a transmission electron microscopy (TEM), and a fourier transform infrared spectrophotometer (FT-IR). XRD and selected area electron diffraction (SAED) patterns assured the formation of TiO2 anatase phase. TEM observation reveled the composition of TiO2 crystallites with about 4 nm in size. Catalyst performance for the ground sample was confirmed by chemical reaction of oxidation of benzene at low temperature, and the difference in catalyst performance between TiO2 AGs with and without the embedded NiB nano-clusters has been examined.

Characterization of high-pressure sintered C60 nanowhiskers and C60 powder

2005 ◽  
Vol 20 (3) ◽  
pp. 742-746 ◽  
Author(s):  
Jun-ichi Minato ◽  
Kun'ichi Miyazawa ◽  
Tadatomo Suga ◽  
Hisao Kanda ◽  
Minoru Akaishi ◽  
...  
Keyword(s):  
High Pressure ◽  
Temperature Treatment ◽  
Precipitation Method ◽  
High Temperature Treatment ◽  
Sintering Process ◽  
X Ray Diffraction ◽  
Treatment Comparison ◽  
Transmission Electron ◽  
Infrared And Raman Spectroscopy

C60 nanowhiskers fabricated by liquid–liquid interfacial precipitation method and pristine C60 powder were sintered at 800 °C under 5.5 GPa for 2 h. The specimens showed high micro-Vickers hardness about 1100 kg/mm2 and electrical resistivity as low as several Ωm. Structural characterization by x-ray diffraction, high-resolution transmission electron microscopy, Fourier transform infrared, and Raman spectroscopy revealed that most of C60 molecules were broken to form turbostratic graphite by high-pressure and high-temperature treatment. Comparison with the pristine C60 powder sintered under the same conditions suggests that the structural change depends microscopically on the C60 molecules, but the size and the morphology of the starting material also affect the macroscopic sintering process.

scholarly journals A Systematic Study of the Effect of pH on the Initialization of Ca-deficient Hydroxyapatite to β-TCP Nanoparticles

Materials ◽  
2019 ◽  
Vol 12 (3) ◽  
pp. 354 ◽  
Author(s):  
Feray Bakan
Keyword(s):  
Precursor Solution ◽  
Temperature Treatment ◽  
High Temperature Treatment ◽  
X Ray Diffraction ◽  
Full Transformation ◽  
High Crystallinity ◽  
Transmission Electron ◽  
Bearing Alloy ◽  
Solution Parameters ◽  
Base Load

The formation of β-tricalcium phosphate (β-TCP) nanoparticles via a wet precipitation technique was studied in a systematical way, taking reaction pH and sintering temperature parameters into account. A full transformation of Ca-deficient hydroxyapatite (CDHA) to β-TCP at 750 °C in under 3 hours from Ca++ and PO43- precursor solutions prepared under a pH of 5.5 was observed. For pH values higher than 6.5, CDHA can only partially transform into β-TCP and only at temperatures higher than 750 °C confirmed using X-Ray diffraction and Raman spectroscopy. The morphologies of the particles were also examined by Transmission electron microscopy. The lower temperatures and the shorter sintering time allow for a fine needle-like morphology, but with a high crystallinity, likely eliminating the possibility of excessive grain growth that is otherwise expected to occur under high-temperature treatment with long process times. We show that sintering of nanostructured, high crystallinity β-TCP at relatively low temperatures is possible via adjustment of the precursor solution parameters. Such an outcome is important for the use of β-TCP with a fine morphology imitating that of the skeletal tissues, enhancing the osteointegration of a base, load-bearing alloy to the host tissue. MTT analysis was used to test the effect of the obtained β-TCP particles on the viability of MG-63 human osteoblast-like cells.

scholarly journals The Influence Of NO/O2 On The NOx Storage Properties Over A Pt-Ba-Ce/γ-Al2O3 Catalyst

2019 ◽  
Vol 17 (1) ◽  
pp. 1459-1465
Author(s):  
Xuedong Feng ◽  
Jing Yi ◽  
Peng Luo
Keyword(s):  
Sol Gel ◽  
Chemical Properties ◽  
No Oxidation ◽  
Test Results ◽  
X Ray Diffraction ◽  
Storage Performance ◽  
Transmission Electron ◽  
Temperature Programmed ◽  
Physical And Chemical ◽  
Al2o3 Catalyst

AbstractWith the purpose of studying the influence of NO/O2 on the NOx storage activity, a Pt-Ba-Ce/γ-Al2O3 catalyst was synthesized by an acid-aided sol-gel method. The physical and chemical properties of the catalyst were characterized by X-ray diffraction (XRD) and Transmission Electron Microscope (TEM) methods. The results showed that the composition of the catalyst was well-crystallized and the crystalline size of CeO2 (111) was about 5.7 nm. The mechanism of NO and NO2 storage and NOx temperature programmed desorption (NO-TPD) experiments were investigated to evaluate the NOx storage capacity of the catalyst. Pt-Ba-Ce/γ-Al2O3 catalyst presented the supreme NOx storage performance at 350℃, and the maximum value reached to 668.8 μmol / gcat. Compared with O2-free condition, NO oxidation to NO2 by O2 had a beneficial effect on the storage performance of NOx. NO-TPD test results showed that the NOx species stored on the catalyst surface still kept relatively stable even below 350℃.

scholarly journals V2O3/C composite fabricated by carboxylic acid-assisted sol–gel synthesis as anode material for lithium-ion batteries

2021 ◽  
Author(s):  
G. S. Zakharova ◽  
E. Thauer ◽  
A. N. Enyashin ◽  
L. F. Deeg ◽  
Q. Zhu ◽  
...  
Keyword(s):  
Electrochemical Performance ◽  
Lithium Ion Batteries ◽  
Sol Gel ◽  
Carbon Sources ◽  
Lithium Ion ◽  
X Ray Diffraction ◽  
Electron Microscopies ◽  
Transmission Electron ◽  
Battery Electrode ◽  
Sol Gel Synthesis

AbstractThe potential battery electrode material V2O3/C has been prepared using a sol–gel thermolysis technique, employing vanadyl hydroxide as precursor and different organic acids as both chelating agents and carbon sources. Composition and morphology of resultant materials were characterized by X-ray diffraction, Raman spectroscopy, scanning and transmission electron microscopies, physical sorption, and elemental analysis. Stability and electronic properties of model composites with chemically and physically integrated carbon were studied by means of quantum-chemical calculations. All fabricated composites are hierarchically structured and consist of carbon-covered microparticles assembled of polyhedral V2O3 nanograins with intrusions of amorphous carbon at the grain boundaries. Such V2O3/C phase separation is thermodynamically favored while formation of vanadium (oxy)carbides or heavily doped V2O3 is highly unlikely. When used as anode for lithium-ion batteries, the nanocomposite V2O3/C fabricated with citric acid exhibits superior electrochemical performance with an excellent cycle stability and a specific charge capacity of 335 mAh g−1 in cycle 95 at 100 mA g−1. We also find that the used carbon source has only minor effects on the materials’ electrochemical performance.

Effect of Calcinations on Characterizations of Fabricated Nano Manganese Ferrite

2013 ◽  
Vol 634-638 ◽  
pp. 2150-2154 ◽  
Author(s):  
Rita Sundari ◽  
Tang Ing Hua ◽  
M. Rusli Yosfiah
Keyword(s):  
Sol Gel ◽  
Volatile Components ◽  
Manganese Ferrite ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Reflectance Analysis ◽  
Transmission Electron Microscope Analysis ◽  
Electron Microscope Analysis ◽  
Nano Size

A citric acid anionic surfactant has been applied for nano manganese ferrite (MnFeO3) fabrication using sol gel method. The calcinations have been varied for 300, 600 and 800oC. The UVDR (UV-Vis Diffused Reflectance) analysis shows a high absorptive band gap after 400 nm for the 600oC calcinated MnFeO3. The DTA (Differential Thermal Analysis) profiles exhibit remarkably trapped volatile matters (H2O, CO2, and NO2) in the fabricated MnFeO3 under sol gel heat treatment at 100oC and the peaks disappeared as the calcination increased to 600oC. As the temperature elevated from 100 to 300oC, the absorption peaks of volatile components are disappeared as demonstrated clearly by the FTIR (Fourier Transform Infrared) spectra of the fabricated material, which 3393 cm-1 corresponded to OH group, 1624 cm-1 to CO group, and 1384 cm-1 to NO group. The XRD (X-Ray Diffraction) spectra show clearly the alteration process from amorphous to crystalline structure as the calcinations increased from 300 to 600oC. In addition, the TEM (Transmission Electron Microscope) analysis exhibits parts of the fabricated MnFeO3 found in cubic nano size of 15-40 nm under interested calcinations and the result is in agreement with that obtained by XRD investigation.

Researches on Preparation of Photosan Loaded Magnetic Silica Anoparticles and their Anti-Tumor Effects in Photodynamic Therapy

2012 ◽  
Vol 622-623 ◽  
pp. 821-826
Author(s):  
Yu Wen ◽  
Xiao Feng Deng ◽  
Liang Liang Liu ◽  
Shu Yun Shi ◽  
Li Xiong
Keyword(s):  
Drug Delivery ◽  
Photodynamic Therapy ◽  
Drug Delivery System ◽  
Delivery System ◽  
Sol Gel ◽  
Haematoporphyrin Derivative ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Good Biocompatibility ◽  
Low Solubility

Photodynamic therapy (PDT) is an effective, noninvasive and nontoxic therapeutics for cancer and some other diseases. It is becoming a alternative of traditional therapeutics for cancers. But the efficacy of PDT was restricted by insufficient selectivity and low solubility. In this study, novel multifunctional silica-based magnetic nanoparticles were prepared as targeting drug delivery system to achieve higher specificity and better solubility. Haematoporphyrin derivative (photosan) was used as photosensitizer. Magnetite nanoparticles (Fe3O4) and photosan were incorporated in silica nanoparticles by microemulsion and sol-gel methods. The prepared nanoparticles were characterized by X-ray diffraction, and transmission electron microscopy. The nanoparticles possessed good biocompatibility and could cause remarkable photodynamic anti-tumor effects. These suggested that photosan-Fe3O4 nanoparticles had great potential as effective drug delivery system in targeting photodynamic therapy.

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.

The effect of silver concentration and calcination temperature on structural and optical properties of ZnO:Ag nanoparticles

2015 ◽  
Vol 29 (01) ◽  
pp. 1450254 ◽  
Author(s):  
M. Shayani Rad ◽  
A. Kompany ◽  
A. Khorsand Zak ◽  
M. E. Abrishami
Keyword(s):  
Calcination Temperature ◽  
Sol Gel ◽  
Visible Emission ◽  
X Ray Diffraction ◽  
Ag Nps ◽  
Zno Nps ◽  
Calcination Temperatures ◽  
Transmission Electron ◽  
Xrd Patterns ◽  
Average Size

Pure and silver added zinc oxide nanoparticles ( ZnO -NPs and ZnO : Ag -NPs) were synthesized through a modified sol–gel method. The prepared samples were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM) and photoluminescence (PL) spectroscopy. In the XRD patterns, silver diffracted peaks were also observed for the samples synthesized at different calcination temperatures of 500°C, 700°C, 900°C except 1100°C, in addition to ZnO . TEM images indicated that the average size of ZnO : Ag -NPs increases with the amount of Ag concentration. The PL spectra of the samples revealed that the increase of Ag concentration results in the increase of the visible emission intensity, whereas by increasing the calcination temperature the intensity of visible emission of the samples decreases.

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