scholarly journals Sensitivity Tests of Pellets Made from Manganese Antimonate Nanoparticles in Carbon Monoxide and Propane Atmospheres

Sensors ◽  
2018 ◽  
Vol 18 (7) ◽  
pp. 2299 ◽  
Author(s):  
Héctor Guillén-Bonilla ◽  
Verónica-M. Rodríguez-Betancourtt ◽  
José Guillen-Bonilla ◽  
Lorenzo Gildo-Ortiz ◽  
Alex Guillen-Bonilla ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Carbon Monoxide ◽  
Gas Sensor ◽  
Hexagonal Structure ◽  
Cell Parameters ◽  
Transmission Electron ◽  
Precursor Material ◽  
Colloidal Method ◽  
Antimony Chloride ◽  
Average Size

Nanoparticles of manganese antimonate (MnSb2O6) were prepared using the microwave-assisted colloidal method for its potential application as a gas sensor. For the synthesis of the oxide, manganese nitrate, antimony chloride, ethylenediamine and ethyl alcohol (as a solvent) were used. The precursor material was calcined at 800 °C in air and analyzed by X-ray diffraction. The oxide crystallized into a hexagonal structure with spatial group P321 and cell parameters a = b = 8.8054 Å and c = 4.7229 Å. The microstructure of the material was analyzed by scanning electron microscopy (SEM), finding the growth of microrods with a size of around ~10.27 μm and some other particles with an average size of ~1.3 μm. Photoacoustic spectroscopy (PAS) studies showed that the optical energy band (Eg) of the oxide was of ~1.79 eV. Transmission electron microscopy (TEM) analyses indicated that the size of the nanoparticles was of ~29.5 nm on average. The surface area of the powders was estimated at 14.6 m2/g by the Brunauer–Emmett–Teller (BET) method. Pellets prepared from the nanoparticles were tested in carbon monoxide (CO) and propane (C3H8) atmospheres at different concentrations (0–500 ppm) and operating temperatures (100, 200 and 300 °C). The pellets were very sensitive to changes in gas concentration and temperature: the response of the material rose as the concentration and temperature increased. The results showed that the MnSb2O6 nanoparticles can be a good candidate to be used as a novel gas sensor.

scholarly journals Gas Sensing Properties of NiSb2O6 Micro- and Nanoparticles in Propane and Carbon Monoxide Atmospheres

2017 ◽  
Vol 2017 ◽  
pp. 1-9 ◽  
Author(s):  
Verónica-M. Rodríguez-Betancourtt ◽  
Héctor Guillén Bonilla ◽  
Martín Flores Martínez ◽  
Alex Guillén Bonilla ◽  
J. P. Moran Lazaro ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Carbon Monoxide ◽  
Gas Sensing ◽  
Average Diameter ◽  
Cell Parameters ◽  
Sensing Applications ◽  
Transmission Electron ◽  
Colloidal Method ◽  
Antimony Chloride ◽  
20 Nm

Micro- and nanoparticles of NiSb2O6 were synthesized by the microwave-assisted colloidal method. Nickel nitrate, antimony chloride, ethylenediamine, and ethyl alcohol were used. The oxide was obtained at 600°C and was analyzed by X-ray diffraction (XRD) and Raman spectroscopy, showing a trirutile-type structure with cell parameters a = 4.641 Å, c = 9.223 Å, and a space group P42/mnm (136). Average crystal size was estimated at ~31.19 nm, according to the XRD-peaks. The microstructure was scrutinized by scanning electron microscopy (SEM), observing microrods measuring ~3.32 μm long and ~2.71 μm wide, and microspheres with an average diameter of ~8 μm; the size of the particles shaping the microspheres was measured in the range of ~0.22 to 1.8 μm. Transmission electron microscopy (TEM) revealed that nanoparticles were obtained with sizes in the range of 2 to 20 nm (~10.7 nm on average). Pellets made of oxide’s powders were tested in propane (C3H8) and carbon monoxide (CO) atmospheres at different concentrations and temperatures. The response of the material increased significantly as the temperature and the concentration of the test gases rose. These results show that NiSb2O6 may be a good candidate for gas sensing applications.

scholarly journals Sensitivity of Mesoporous CoSb2O6Nanoparticles to Gaseous CO and C3H8at Low Temperatures

2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Héctor Guillén-Bonilla ◽  
Lorenzo Gildo-Ortiz ◽  
M. de la L. Olvera-Amador ◽  
Jaime Santoyo-Salazar ◽  
Verónica M. Rodríguez-Betancourtt ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Gas Sensors ◽  
Low Temperatures ◽  
Cobalt Nitrate ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Precursor Material ◽  
Means Of Transmission ◽  
Average Size

Mesoporous CoSb2O6nanoparticles, synthesized through a nonaqueous method (using cobalt nitrate, antimony trichloride, ethylenediamine, and ethanol as a solvent), were tested to establish their sensitivity to CO and C3H8atmospheres at relatively low temperatures. The precursor material was dried at 200°C and calcined at 600°C. X-ray diffraction and scanning electron microscopy were employed to verify the existence of crystal phases (P42/mnm) and the morphology of this trirutile-type CoSb2O6oxide. Pyramidal and cubic shaped crystals (average size: 41.1 nm), embedded in the material’s surface, were identified. Mesopores (average size: 6.5 nm) on the nanoparticles’ surface were observed by means of transmission electron microscopy. The best sensitivity of the CoSb2O6in a CO atmosphere was at the relatively low temperatures of 250 and 350°C, whereas, in a C3H8atmosphere, the sensitivity increased uniformly with temperature. These results encourage using the CoSb2O6nanoparticles as gas sensors.

scholarly journals Study on Structure, Thermal Behavior, and Viscoelastic Properties of Nanodiamond-Reinforced Poly (vinyl alcohol) Nanocomposites

Polymers ◽  
2021 ◽  
Vol 13 (9) ◽  
pp. 1426
Author(s):  
Tomáš Remiš ◽  
Petr Bělský ◽  
Tomáš Kovářík ◽  
Jaroslav Kadlec ◽  
Mina Ghafouri Azar ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Mechanical Analysis ◽  
Single Step ◽  
Poly Vinyl Alcohol ◽  
Scanning Calorimetry ◽  
X Ray Scattering ◽  
Transmission Electron ◽  
Primary Particles ◽  
Solution Casting Method ◽  
Average Size

In this work, advanced polymer nanocomposites comprising of polyvinyl alcohol (PVA) and nanodiamonds (NDs) were developed using a single-step solution-casting method. The properties of the prepared PVA/NDs nanocomposites were investigated using Raman spectroscopy, small- and wide-angle X-ray scattering (SAXS/WAXS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and dynamic mechanical analysis (DMA). It was revealed that the tensile strength improved dramatically with increasing ND content in the PVA matrix, suggesting a strong interaction between the NDs and the PVA. SEM, TEM, and SAXS showed that NDs were present in the form of agglomerates with an average size of ~60 nm with primary particles of diameter ~5 nm. These results showed that NDs could act as a good nanofiller for PVA in terms of improving its stability and mechanical properties.

Preparation of Poly(Vinylbenzyl Chloride)@Lead Sulfide (PVBC@PbS) Core-Shell Nanospheres and Adsorption of Phenol

2013 ◽  
Vol 704 ◽  
pp. 270-274 ◽  
Author(s):  
Jian Ye ◽  
Lan Ping Sun ◽  
Sheng Ping Gao
Keyword(s):  
Electron Microscopy ◽  
Lead Sulfide ◽  
Chemical Structure ◽  
Methyl Chloride ◽  
Core Shell ◽  
Subsequent Reaction ◽  
Chloride Lead ◽  
Transmission Electron ◽  
The Fourier Transform ◽  
Average Size

We have demonstrated the fabrication of novel poly(vinylbenzyl chloride)@lead sulfide (PVBC@PbS) core-shell nanospheres via the atom transfer reversible polymerization (ATRP) of lead dimethacrylate (Pb(MA)2) initiated from methyl chloride groups on surfaces of PVBC nanoparticles and subsequent reaction with ethanethioamide. The chemical structure of the PVBC@PbS nanospheres was confirmed by the fourier transform infrared (FTIR) spectroscopy, and the morphology of the nanospheres were investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The average size of the nanospheres was determined to be about 100 nm. The PVBC@PbS nanospheres were able to absorb phenol in the solution, and the balanced adsorption capability of phenol to nanospheres could reach to 7.2 μg/mg.

scholarly journals Formation of ZnO/Zn0.5Cd0.5Se Alloy Quantum Dots in the Presence of High Oleylamine Contents

Nanomaterials ◽  
2019 ◽  
Vol 9 (7) ◽  
pp. 999
Author(s):  
Yi-An Chen ◽  
Kuo-Hsien Chou ◽  
Yi-Yang Kuo ◽  
Cheng-Ye Wu ◽  
Po-Wen Hsiao ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Quantum Dots ◽  
Particle Size ◽  
X Ray Diffraction ◽  
One Pot ◽  
X Ray ◽  
Transmission Electron ◽  
Average Size ◽  
Alloy Quantum Dots ◽  
First Time

To the best of our knowledge, this report presents, for the first time, the schematic of the possible chemical reaction for a one-pot synthesis of Zn0.5Cd0.5Se alloy quantum dots (QDs) in the presence of low/high oleylamine (OLA) contents. For high OLA contents, high-resolution transmission electron microscopy (HRTEM) results showed that the average size of Zn0.5Cd0.5Se increases significantly from 4 to 9 nm with an increasing OLA content from 4 to 10 mL. First, [Zn(OAc)2]–OLA complex can be formed by a reaction between Zn(OAc)2 and OLA. Then, Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD) data confirmed that ZnO is formed by thermal decomposition of the [Zn(OAc)2]–OLA complex. The results indicated that ZnO grew on the Zn0.5Cd0.5Se surface, thus increasing the particle size. For low OLA contents, HRTEM images were used to estimate the average sizes of the Zn0.5Cd0.5Se alloy QDs, which were approximately 8, 6, and 4 nm with OLA loadings of 0, 2, and 4 mL, respectively. We found that Zn(OAc)2 and OLA could form a [Zn(OAc)2]–OLA complex, which inhibited the growth of the Zn0.5Cd0.5Se alloy QDs, due to the decreasing reaction between Zn(oleic acid)2 and Se2−, which led to a decrease in particle size.

Structural characterization of SmMn2GeO7 single microcrystals by electron microscopy

2005 ◽  
Vol 61 (1) ◽  
pp. 11-16 ◽  
Author(s):  
E. A. Juarez-Arellano ◽  
J. M. Ochoa ◽  
L. Bucio ◽  
J. Reyes-Gasga ◽  
E. Orozco
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Structural Characterization ◽  
Point Group ◽  
Spherical Mirror ◽  
Quaternary Compound ◽  
Cell Parameters ◽  
Transmission Electron ◽  
Electron Energy Loss

Single microcrystals of the new compound samarium dimanganese germanium oxide, SmMn2GeO7, were grown using the flux method in a double spherical mirror furnace (DSMF). The micrometric crystals were observed and chemically analysed with scanning electron microscopy (SEM) and X-ray energy dispersive spectroscopy (EDX). The structural characterization and chemical analysis of these crystals were also carried out using transmission electron microscopy (TEM) and high-resolution transmission electron microscopy (HRTEM), together with electron-energy-loss spectroscopy (EELS). We found that the new quaternary compound crystallizes in the orthorhombic system with the point group mmm (D 2h ), space group Immm (No. 71) and cell parameters a = 8.30 (10), b = 8.18 (10), c = 8.22 (10) Å and V = 558.76 Å3.

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.

scholarly journals Gold Particle Size Determination on Au/TiO2-CeO2 Catalysts by Means of Carbon Monoxide, Hydrogen Chemisorption and Transmission Electron Microscopy

2009 ◽  
Vol 5 ◽  
pp. 13-23 ◽  
Author(s):  
C. Guzmán ◽  
Gloria Del Angel ◽  
Ricardo Gómez ◽  
F. Galindo ◽  
R. Zanella ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Carbon Monoxide ◽  
Particle Size ◽  
Gold Particle ◽  
Precipitation Method ◽  
Hydrogen Chemisorption ◽  
Gold Particles ◽  
Transmission Electron ◽  
Gold Particle Size

Au/TiO2 and Au/TiO2-CeO2 catalysts were prepared by the sol-gel method and carbon monoxide, hydrogen chemisorption and TEM spectroscopy have been exploited to determine the size of gold particles. The gold nanoparticles (8.1 to 2.1 nm) were deposited by using the deposition-precipitation method. The XRD characterization shows the presence of anatase as the TiO2 crystalline phase; while by XPS spectroscopy, the presence of Au°, Au2O3, Ce3+ and Ce4+ species co-existing in the Au/TiO2-CeO2 catalysts is shown. The characterizations by TPD-CO as well as by TPD-H2 (temperature programmed desorption) showed that on catalysts containing cerium, the gold particle size can be determined with great accuracy by using these chemisorption methods. The gold particle size calculated from either the CO or H2 thermodesorption values is in good agreement with that obtained by High Resolution Transmission Electron Microscopy (HRTEM) and Scanning Transmission Electron Microscopy (STEM) analyses. It was proposed that the TPD-CO and/or TPD-H2 techniques could be helpful for the characterization of the gold particles by TEM; especially when the high contrast in the pictures of the supports containing CeO2 prevents the particle size from being determined.

HRTEM Investigation of Precipitates in Al-Zn-In-Mg-Ti-Ce Anode Alloy

2011 ◽  
Vol 189-193 ◽  
pp. 1036-1039
Author(s):  
Jing Ling Ma ◽  
Jiu Ba Wen ◽  
Yan Fu Yan
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
High Resolution ◽  
Electron Diffraction ◽  
Hexagonal Structure ◽  
Orientation Relation ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Scanning Electron

The precipitates of Al-5Zn-0.02In-1Mg-0.05Ti-0.5Ce (wt %) anode alloy were studied by scanning electron microscopy, X-ray microanalysis, high resolution transmission electron microscopy and selected area electron diffraction analyses in the present work. The results show that the alloy mainly contains hexagonal structure MgZn2 and tetragonal structure Al2CeZn2 precipitates. From high resolution transmission electron microscopy and selected area electron diffraction, aluminium, Al2CeZn2 and MgZn2 phases have [0 1 -1]Al|| [1 -10]Al2CeZn2|| [-1 1 0 1]MgZn2orientation relation, and Al2CeZn2 and MgZn2 phases have the [0 2 -1]Al2CeZn2|| [0 1 -10]MgZn2orientation relation.

Characterization of Zn0.96Al0.02Ga0.02O Thermoelectric Material

2013 ◽  
Vol 802 ◽  
pp. 227-231
Author(s):  
Panida Pilasuta ◽  
Pennapa Muthitamongkol ◽  
Chanchana Thanachayanont ◽  
Tosawat Seetawan
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Single Phase ◽  
Hexagonal Structure ◽  
Hexagonal Crystal Structure ◽  
X Ray Diffraction ◽  
Hexagonal Crystal ◽  
X Ray ◽  
Transmission Electron

Crystal structure of Zn0.96Al0.02Ga0.02O was analyzed by X-Ray diffraction (XRD) technique and the microstructure was observed by scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The XRD results showed single phase and hexagonal structure a = b = 3.24982 Å, and c = 5.20661 Å. The SEM and TEM results showed the grain size of material arrangement changed after sintering and TEM diffraction pattern confirmed hexagonal crystal structure of Zn0.96Al0.02Ga0.02O after sintering.

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