Fabrication of Gelatin-Zr (IV) Phosphate and Alginate-Zr (IV) Phosphate Nanocomposite Based Ion Selective Membrane Electrode

2018 ◽  
Vol 20 ◽  
pp. 108-120 ◽  
Author(s):  
Manita Thakur ◽  
Deepak Pathania
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
Membrane Electrode ◽  
Membrane Electrodes ◽  
Ion Exchangers ◽  
Selective Electrode ◽  
Transmission Electron ◽  
Selective Membrane ◽  
Ph Range ◽  
Scanning Electron

Gelatin- Zr (IV) phosphate nanocomposite (GT@ZPNC) and alginate- Zr (IV) phosphate nanocomposite (AG@ZPNC) ion exchangers has been prepared by sol-gel method. The nanocomposites are characterised by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The SEM results of GT@ZPNC and AG@ZPNC confirmed that after the binding of polymer matrix to inorganic part, morphology was completely reformed. TEM results confirmed the synthesised materials were nanocomposite in nature. The GT@ZPNC and AG@ZPNC ion exchangers have been explored to fabricate ion selective electrode for the detection of Cd (II) and Al (III) metal ions. Both ion selective membrane electrodes show wide working concentration and pH range with good response time.

Synthesis and Thermal Stability of Nontransformable Tetragonal (ZrO2)0.96(REO1.5)0.04 (Re=Sc3+, Y3+) Nanocrystals

2013 ◽  
Vol 334-335 ◽  
pp. 60-64 ◽  
Author(s):  
Mohammad Reza Loghman-Estark ◽  
Reza Shoja Razavi ◽  
Hossein Edris
Keyword(s):  
Electron Microscopy ◽  
Thermal Stability ◽  
Scanning Electron Microscopy ◽  
Sol Gel ◽  
Average Diameter ◽  
X Ray ◽  
Transmission Electron ◽  
20 Nm ◽  
Thermal Stability Of ◽  
Scanning Electron

Scandia, yttria doped zirconia ((ZrO2)0.96(REO1.5)0.04(RE=Sc3+, Y3+)) nanoparticles were prepared by the modified sol-gel method. The microstructure of the products was characterized by X-ray diffractometry (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Raman spectroscopy. Thermal stabillity of SYSZ nanocrystals were also investigated. The SYSZ nanocrystals synthesized with EGM:Zr+4mole ratio 4:1, calcined at 700°C, have average diameter of ~20 nm.

The Synthesis of Maghemite and Hematite (γ-Fe2O3, α-Fe2O3) Nanospheres

2007 ◽  
Vol 534-536 ◽  
pp. 157-160 ◽  
Author(s):  
M.A. Dar ◽  
S.G. Ansari ◽  
Rizwan Wahab ◽  
Young Soon Kim ◽  
Hyung Shik Shin
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Iron Oxide ◽  
Pore Size ◽  
Field Emission ◽  
Sol Gel ◽  
Oxide Powder ◽  
Transmission Electron ◽  
Scanning Electron

Maghemite and hematite nanospheres were synthesized by using the Sol-gel technique. The structural properties of these nanosphere powders were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM),and pore size distribution.Hematite phase shows crystalline structures.The mean particle size that resulted from BET and XRD analyses were 4.9 nm and 2 nm. The field emission scanning electron microscopy shows iron-oxide powder is composed of nanosized particles, but in nanosized aggregates (agglomeration of particles). It can be seen from transmission electron microscopy that the size of the particles are very small which is in good agreement with the FESEM and the Xray diffraction. TEM and FESEM confirmed that the iron-oxide powder is composed of sizes from 8 nm to 10 nm. The BET and pore size method were employed for specific surface area determination.

scholarly journals Effects of Varying Alx Moles on the Structure and Luminescence Properties of ZnAlxO1.5x + 1:0.1% Tb3+ Nano Phosphor Prepared using Citrate sol-gel Method

2021 ◽  
Author(s):  
V Maphiri ◽  
L Melato ◽  
Mhlongo ◽  
TT Hlatshwayo ◽  
TE Motaung ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Electron Microscopy ◽  
Single Phase ◽  
Sol Gel ◽  
Gel Method ◽  
X Ray ◽  
Sol Gel Method ◽  
Transmission Electron ◽  
Nano Phosphor ◽  
Scanning Electron

Abstract Un-doped and ZnAlxO(1.5x + 1):0.1% Tb3+ (ZAOT) nano-powders were synthesized via citrate sol-gel method. The Alx moles were varied in the range of 0.25 ≤ x ≤ 5.0. The X-ray powder diffraction (XRD) data revealed that for the x < 1.5, the prepared samples crystal structure consists of mixed phases of the cubic ZnAl2O4 and hexagonal ZnO phases, while for the x ≥ 1.5 the structure consists of single phase of cubic ZnAl2O4. This was confirmed by the Raman and Fourier-Transform Infrared (FTIR) vibrational spectroscopy. Scanning electron microscopy (SEM) showed that varying Alx moles influences the morphology while Transmission electron microscopy (TEM) shows the dual morphology at x < 1.5. The photoluminescence (PL) revealed intense and distinct emissions attributed to both the host and Tb3+ transitions. The emission intensity highly depends on the Alx moles. The International Commission on Illumination (CIE) colour chromaticity showed that the emission colour could be tuned by varying the Alx moles.

A Metastable Ion (III) Oxide Phase (ε-Fe2O3): Preparation and Gas Sensing Properties

2016 ◽  
Vol 697 ◽  
pp. 737-740 ◽  
Author(s):  
Ming Jing Wang ◽  
Hui Ming Ji ◽  
Ya Lu Chen ◽  
Qian Qian Jia
Keyword(s):  
Electron Microscopy ◽  
Gas Sensing ◽  
Sol Gel ◽  
Oxide Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Gas Sensing Properties ◽  
Addition Amount ◽  
Scanning Electron

ε-Fe2O3 is a rare and metastable iron (III) oxide phase. ε-Fe2O3/SiO2 composites were prepared by combining the reverse-micelle and sol-gel methods. An appropriate amount of Ba2+ was needed in this system to promote the formation of ε-Fe2O3 nanorods in SiO2. The size of nanorods varied with different Ba2+ addition amount and sintering procedure. Then pure ε-Fe2O3 nanorods were obtained after stripping SiO2 by etching due to NaOH aqueous solution. The as-synthesized ε-Fe2O3 nanorods were discussed using X-ray diffraction (XRD), scanning electron microscope (SEM) and transmission electron microscopy (TEM). Interestingly, metastable ε-Fe2O3 nanorods showed a promising performance for the response for ethanol, compared with the stable phases of α-Fe2O3 and γ-Fe2O3. It indicates that nanostructure ε-Fe2O3 (including ε-Fe2O3 nanorods) could be a valuable material for the fabrication of advanced sensing devices.

Preparation of Alumina Powders through Pyrocatechol, Resorcinol Mediated Sol-Gel Method

2016 ◽  
Vol 850 ◽  
pp. 742-747
Author(s):  
Xiang Zhang ◽  
Ping Yun Li ◽  
Xiao De Guo ◽  
Ting Yan
Keyword(s):  
Electron Microscopy ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Grain Sizes ◽  
Xrd Study ◽  
Transmission Electron ◽  
Sol Gel Process ◽  
Scanning Electron ◽  
Organic Monomer

Ultrafine alumina powders were synthesized through pyrocatechol and resorcinol mediated sol-gel process. Aluminum nitrate was applied as the Al source and PVP was the dispersant. X-ray diffraction (XRD) study displayed that γ-Al2O3 powders formed in the range of 800-900 °C, and then γ-Al2O3 transformed to α-Al2O3 at higher temperatures, pure α-Al2O3 powders could be obtained at 1000 °C by using resorcinol as organic monomer. The results of transmission electron microscopy (TEM) revealed that Al2O3 nanoparticles with γ crystalline phase had grain sizes in the range of 5-40 nm. Scanning electron microscopy (SEM) observation displayed that the morphology of the prepared α-Al2O3 powders had aggregated bodies formed by Al2O3 grains in the range of 0.2-0.5μm. These results provide a new way of preparation of alumina powders.

scholarly journals Synthesis of hybrid amorphous/crystalline SnO2 1D nanostructures: investigation of morphology, structure and optical properties

2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Wiktor Matysiak ◽  
Tomasz Tański ◽  
Weronika Smok ◽  
Oleg Polishchuk
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Energy Gap ◽  
Energy Dispersive Spectrometer ◽  
Sol Gel ◽  
Band Gaps ◽  
1D Nanostructures ◽  
Transmission Electron ◽  
Chloride Pentahydrate ◽  
Scanning Electron

Abstract The aim of the study was to prepare SnO2 nanowires via a combination of electrospinning and the sol–gel method from a polyvinylpyrrolidone (PVP)/dimetylformamide (DMF)/ethanol(EtOH)/tin(IV) chloride pentahydrate (SnCl4·5H2O) solution. The morphology, structure and chemical composition of the obtained PVP/SnO2 nanofibers and SnO2 nanowires were examined using transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) as well as a scanning electron microscope (SEM) with an energy dispersive spectrometer (EDX). The optical property analysis was performed on the basis of UV–Vis spectra of absorbance as a function of the wavelength, based on which the rated values of band gaps of the fabricated 1D nanostructures were determined. The morphology analysis showed that the obtained amorphous SnO2 nanowires with crystalline protuberances were characterized by a diameter of 50 to 120 nm. Results demonstrated that nanowires with a ratio of 1:1 precursor to polymer in the spinning solution were characterized by the smallest diameter after calcination and the smallest energy gap of 3.3 eV among all investigated samples. The rest of the studied materials were characterized by a larger energy gap (3.8 and 3.9 eV).

scholarly journals Effect of Sintering Temperatures on the Synthesis of SnO2 Nanospheres

2012 ◽  
Vol 2012 ◽  
pp. 1-7 ◽  
Author(s):  
Bharat G. Pawar ◽  
Dipak V. Pinjari ◽  
Sanjay S. Kolekar ◽  
Aniruddha B. Pandit ◽  
Sung H. Han
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Large Scale ◽  
Sol Gel ◽  
Visible Region ◽  
Optoelectronic Devices ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

In this communication we report the rapid nanostructure of SnO2 with a spherical morphology which has been prepared in large scale via sol-gel method. The products were characterized with scanning electron microscopy, X-ray powder diffraction, transmission electron microscopy, FTIR, and photoluminescence spectroscopy. The strong photoluminescence of the nanosphere in visible region suggested possible application in nanoscaled optoelectronic devices. A possible growth mechanism for the SnO2 nanosphere in terms of solvation, hydrolysis, and polymerization was proposed.

Morphology dependence of 1,2-diphenylethylenediamine-derived organogelator templates in solvents and their influence in the production of nanostructured silica

2011 ◽  
Vol 65 (4) ◽  
Author(s):  
Tae Kim ◽  
Euh Jeong ◽  
Chae Oh ◽  
Myung Hyun ◽  
Mee Lee ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Sol Gel ◽  
Outer Diameter ◽  
Transmission Electron ◽  
Tetraethoxy Silane ◽  
Inner Diameter ◽  
Nanostructured Silica ◽  
Scanning Electron ◽  
Made In

AbstractThe 1,2-diphenylethylenediamine-based neutral or cationic organogelator-templates, currently employed in the production of silica nanomaterials, were initially evaluated for their versatile gelation ability and found to be gelled in the majority of organic solvents tested. Scanning electron microscope and transmission electron microscope, images of neutral organogels made from different solvents revealed that they assembled into a plate-shaped, or rod-shaped morphology, respectively in ethanol or butan-1-ol and in acetonitrile or tetrahydrofurane. Similarly, a 1: 1 mixture (mass) of neutral and cationic gelators formed different morphologies in the solvents tested. Sol-gel polycondensation of tetraethoxy silane using either individual gels (neutral or cation) or a 1: 1 mixture of gels was explored. The experimental results and the scanning electron microscopy and transmission electron microscopy images revealed that silica nanotubes with an inner diameter of 82 nm and an outer diameter of 620 nm were obtained from the 1: 1 mixture of neutral and cationic gelator in ethanol, whereas silica nanoparticles were obtained using gels made in the other solvents tested.

Ultrastructural Analysis of the Salivary Glands of Gromphadorhina Portentosa (Schaum)

1977 ◽  
Vol 35 ◽  
pp. 638-639
Author(s):  
P.J. Dailey
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Salivary Glands ◽  
Secretory Vesicles ◽  
The Past ◽  
Transmission Electron ◽  
Means Of Transmission ◽  
Gromphadorhina Portentosa ◽  
Scanning Electron ◽  
Topographical Relief

The structure of insect salivary glands has been extensively investigated during the past decade; however, none have attempted scanning electron microscopy (SEM) in ultrastructural examinations of these secretory organs. This study correlates fine structure by means of SEM cryofractography with that of thin-sectioned epoxy embedded material observed by means of transmission electron microscopy (TEM).Salivary glands of Gromphadorhina portentosa were excised and immediately submerged in cold (4°C) paraformaldehyde-glutaraldehyde fixative1 for 2 hr, washed and post-fixed in 1 per cent 0s04 in phosphosphate buffer (4°C for 2 hr). After ethanolic dehydration half of the samples were embedded in Epon 812 for TEM and half cryofractured and subsequently critical point dried for SEM. Dried specimens were mounted on aluminum stubs and coated with approximately 150 Å of gold in a cold sputtering apparatus.Figure 1 shows a cryofractured plane through a salivary acinus revealing topographical relief of secretory vesicles.

Two- or three-way observations of the identical cell elements within the same sections by LM, TEM and/or SEM

1978 ◽  
Vol 36 (2) ◽  
pp. 82-83 ◽  
Author(s):  
Nakazo Watari ◽  
Yasuaki Hotta ◽  
Yoshio Mabuchi
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Fine Structure ◽  
Light Microscopy ◽  
Thin Sections ◽  
Transmission Electron ◽  
Identical Cell ◽  
Electron Microscopes ◽  
Scanning Electron

It is very useful if we can observe the identical cell elements within the same sections by light microscopy (LM), transmission electron microscopy (TEM) and/or scanning electron microscopy (SEM) sequentially, because, the cell fine structure can not be indicated by LM, while the color is; on the other hand, the cell fine structure can be very easily observed by EM, although its color properties may not. However, there is one problem in that LM requires thick sections of over 1 μm, while EM needs very thin sections of under 100 nm. Recently, we have developed a new method to observe the same cell elements within the same plastic sections using both light and transmission (conventional or high-voltage) electron microscopes.In this paper, we have developed two new observation methods for the identical cell elements within the same sections, both plastic-embedded and paraffin-embedded, using light microscopy, transmission electron microscopy and/or scanning electron microscopy (Fig. 1).

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