Solution-Based Synthesis of Magnesium Oxide Nanorods

1999 ◽  
Vol 581 ◽  
Author(s):  
Q. Wei ◽  
C.M. Lieber
Keyword(s):  
Electron Microscopy ◽  
Magnesium Oxide ◽  
Magnesium Chloride ◽  
Low Cost ◽  
Industrial Applications ◽  
Transformation Process ◽  
Matrix Composites ◽  
X Ray ◽  
Transmission Electron ◽  
Oxide Nanorods

ABSTRACTA solution-based synthesis route was developed to produce large quantities of MgO nanorods. Hydrated basic magnesium chloride, which has needle-like crystal structure, was used as a precursor. A subsequent two-step transformation process with magnesium hydroxide as an intermediate product was used to preserve the morphology of the precursor to yield magnesium oxide nanorods. Scanning electron microscopy, powder X-ray diffraction and energy dispersive X-ray spectroscopy show that the products are very pure (>95%) crystalline MgO nanorods with diameters from 40 nm to 200 nm and lengths 10 microns or longer. High-resolution transmission electron microscopy and electron diffraction further reveal that these MgO nanorods are single crystals and that the rod axis is along the <110> crystal direction. A model for the structural transformation from hydrated basic magnesium chloride to magnesium oxide has been developed and compared to our experimental results. This solution-based process can be easily scaled-up, and is a low-cost source of pure magnesium oxide nanorods needed in many industrial applications, for example, as reinforcing agents in matrix composites and as flux-pinning centers in high-TC superconductors.

scholarly journals Chemical Stability of Ti3C2 MXene with Al in the Temperature Range 500–700 °C

Materials ◽  
2018 ◽  
Vol 11 (10) ◽  
pp. 1979 ◽  
Author(s):  
Jing Zhang ◽  
Shibo Li ◽  
Shujun Hu ◽  
Yang Zhou
Keyword(s):  
Electron Microscopy ◽  
Chemical Stability ◽  
Metal Matrix ◽  
Matrix Composites ◽  
X Ray Diffraction ◽  
X Ray ◽  
Temperature Range ◽  
Transmission Electron ◽  
Work First ◽  
Scanning Electron

Ti3C2Tx MXene, a new 2D nanosheet material, is expected to be an attractive reinforcement of metal matrix composites because its surfaces are terminated with Ti and/or functional groups of –OH, –O, and –F which improve its wettability with metals. Thus, new Ti3C2Tx/Al composites with strong interfaces and novel properties are desired. To prepare such composites, the chemical stability of Ti3C2Tx with Al at high temperatures should be investigated. This work first reports on the chemical stability of Ti3C2Tx MXene with Al in the temperature range 500–700 °C. Ti3C2Tx is thermally stable with Al at temperatures below 700 °C, but it reacts with Al to form Al3Ti and TiC at temperatures above 700 °C. The chemical stability and microstructure of the Ti3C2Tx/Al samples were investigated by differential scanning calorimeter, X-ray diffraction analysis, scanning electron microscopy, and transmission electron microscopy.

scholarly journals A Novel X-Ray Radiation Sensor Based on Networked SnO2 Nanowires

2019 ◽  
Vol 9 (22) ◽  
pp. 4878 ◽  
Author(s):  
Jae-Hun Kim ◽  
Ali Mirzaei ◽  
Hyoun Woo Kim ◽  
Hong Joo Kim ◽  
Phan Quoc Vuong ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Room Temperature ◽  
Low Cost ◽  
X Rays ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Radiation Sensor ◽  
Sno2 Nanowires ◽  
Radiation Sensors

X-Ray radiation sensors that work at room temperature are in demand. In this study, a novel, low-cost real-time X-ray radiation sensor based on SnO2 nanowires (NWs) was designed and tested. Networked SnO2 NWs were produced via the vapor–liquid–solid technique. X-ray diffraction (XRD), transmission electron microscopy (TEM) and field emission scanning electron microscopy (SEM) analyses were used to explore the crystallinity and morphology of synthesized SnO2 NWs. The fabricated sensor was exposed to X-rays (80 kV, 0.0–2.00 mA) and the leakage current variations were recorded at room temperature. The SnO2 NWs sensor showed a high and relatively linear response with respect to the X-ray intensity. The X-ray sensing results show the potential of networked SnO2 NWs as novel X-ray sensors.

Synthesis and characterization of tungsten oxide nanorods

2004 ◽  
Vol 19 (12) ◽  
pp. 3665-3670 ◽  
Author(s):  
D.Z. Guo ◽  
K. Yu-Zhang ◽  
A. Gloter ◽  
G.M. Zhang ◽  
Z.Q. Xue
Keyword(s):  
Electron Microscopy ◽  
Tungsten Oxide ◽  
Electric Heating ◽  
Tungsten Oxides ◽  
X Ray ◽  
Preparation Conditions ◽  
Transmission Electron ◽  
Oxide Nanorods ◽  
Electron Energy Loss

Single crystalline nanorods (15–200 nm in diameter and hundreds nanometers in length) have been formed on the carbon-covered W wires by simple electric heating under a vacuum of 5 × 10−4 Pa. The chemical composition and crystalline structure of the nanorods were carefully investigated by various characterization techniques such as scanning electron microscopy, transmission electron microscopy, Raman spectroscopy, energy dispersive x-ray spectroscopy and electron energy loss spectroscopy. After ruling out any possible existence of carbon nanotubes (CNTs), tungsten carbide, W–Fe alloying, and formation of other types of tungsten oxides, monoclinic W18O49 phase has been well identified. The mechanism of nanorod formation of sub-tungsten oxide (∼WO2.7 compared to WO3) will be discussed in relation to the sample preparation conditions.

Novel synthesis of AlN nanowires with controlled diameters

2001 ◽  
Vol 16 (11) ◽  
pp. 3133-3138 ◽  
Author(s):  
Jun Liu ◽  
X. Zhang ◽  
Yingjiu Zhang ◽  
Rongrui He ◽  
Jing Zhu
Keyword(s):  
Electron Microscopy ◽  
Carbon Nanotubes ◽  
High Efficiency ◽  
Low Cost ◽  
X Ray Diffraction ◽  
Synthesis Mechanism ◽  
X Ray ◽  
Novel Synthesis ◽  
Transmission Electron ◽  
New Synthesis

A relatively low-cost, high-efficiency method is reported to synthesize AlN nanowires, using carbon nanotubes as templates. The AlN nanowires were fabricated at 1100 °C, for 60 min. The diameters of the product could be roughly controlled by the sizes of carbon nanotubes selected as starting materials. The AlN nanowires obtained were among the thinnest ever known. X-ray diffraction, selected-area diffraction, energy dispersive spectroscopy, and high-resolution transmission electron microscopy, etc. were employed to characterize the products, which were found to be single crystals with some defects. The axes of the nanowires are normal to {1010} crystal planes. A new synthesis mechanism is proposed.

scholarly journals Structural Characterization and Adsorption Properties of Dunino Raw Halloysite Mineral for Dye Removal from Water

Materials ◽  
2021 ◽  
Vol 14 (13) ◽  
pp. 3676
Author(s):  
Simona Filice ◽  
Corrado Bongiorno ◽  
Sebania Libertino ◽  
Giuseppe Compagnini ◽  
Leon Gradon ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Dye Removal ◽  
Low Cost ◽  
Point Of Zero Charge ◽  
Tubular Structures ◽  
Iron Oxide Particles ◽  
X Ray ◽  
Transmission Electron ◽  
Oxide Particles ◽  
Electron Energy Loss

In this work, raw halloysite mineral from Dunino (Poland) has been characterized and tested as an efficient and low-cost adsorbent for dye removal from water. The morphology and structure of this clay were characterized using scanning electron microscopy (SEM) and transmission electron microscopy (TEM) and the chemical composition was evaluated by means of X-ray fluorescence spectroscopy (XRF), energy dispersive X-ray spectroscopy (EDX), and electron energy loss spectroscopy (EELS). The results showed that it is made up of both platy and tubular structures, mainly composed of Si, Al, and O. Iron oxide particles covering the platy structures were also observed. The surface charge of halloysite was measured by z-potential measurements and by the evaluation of the point of zero charge. The clay was tested as an adsorbent for the removal of positively and negatively charged dye molecules, i.e., methylene blue (MB) and methyl orange (MO), both separately and in a mixed-dye solution. Halloysite showed the ability to efficiently and selectively remove MB molecules by adsorption, both in a single-dye solution and in a mixed one. The adsorption of positive dyes on the clay surface mainly occurred through ion exchange at negatively charged sites on its surface. The possibility of regenerating the clay for further dye removal processes is also shown.

scholarly journals Effects of Pr and Yb Dual Doping on the Thermoelectric Properties of CaMnO3

Materials ◽  
2018 ◽  
Vol 11 (10) ◽  
pp. 1807 ◽  
Author(s):  
Cuiqin Li ◽  
Qianlin Chen ◽  
Yunan Yan
Keyword(s):  
Electron Microscopy ◽  
Figure Of Merit ◽  
Low Cost ◽  
X Ray Diffraction ◽  
Thermoelectric Figure ◽  
X Ray ◽  
Transmission Electron ◽  
New Strategy ◽  
Low Toxicity

There has been research on CaMnO3 with natural abundance, low toxicity, and low cost as promising candidates for n-type thermoelectric (TE) materials. In this paper, Ca1−2xPrxYbxMnO3 with different Pr and Yb contents (x = 0, 0.01, 0.02, 0.03, 0.04 and 0.05) were synthesized by means of coprecipitation. With X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM), researchers characterized the phase structure and morphology of all the samples. The oxidation states of manganese were determined by X-ray photoemission spectroscopy (XPS). The role of Ca-site dual doping in the TE properties was also investigated. Increasing the Pr and Yb contents leads to decreases in the electrical resistivity and Seebeck coefficient, leading to a power factor of 3.48 × 10−4 W·m−1·K−2 for x = 0.04 at 773 K, which is its maximum. Furthermore, the thermal conductivity (κ) decreases with increasing x, and κ = 1.26 W m−1·K−1 is obtained for x = 0.04 at 973 K. Ca0.92Pr0.04Yb0.04MnO3 exhibit a ZT (thermoelectric figure of merit) value of 0.24 at 973 K, approximately 3 times more than that of the pristine CaMnO3. Thus, the reported method is a new strategy to enhance the TE performance of CaMnO3.

scholarly journals Facile Synthesis of Calcium Carbonate Nanoparticles from Cockle Shells

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Kh. Nurul Islam ◽  
A. B. Z. Zuki ◽  
M. E. Ali ◽  
Mohd Zobir Bin Hussein ◽  
M. M. Noordin ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Calcium Carbonate ◽  
Large Scale ◽  
Low Cost ◽  
Analytical Techniques ◽  
Variable Pressure ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Ft Ir

A simple and low-cost method for the synthesis of calcium carbonate nanoparticles from cockle shells was described. Polymorphically, the synthesized nanoparticles were aragonites which are biocompatible and thus frequently used in the repair of fractured bone and development of advanced drug delivery systems, tissue scaffolds and anticarcinogenic drugs. The rod-shaped and pure aragonite particles of30±5 nm in diameter were reproducibly synthesized when micron-sized cockle shells powders were mechanically stirred for 90 min at room temperature in presence of a nontoxic and nonhazardous biomineralization catalyst, dodecyl dimethyl betaine (BS-12). The findings were verified using a combination of analytical techniques such as variable pressure scanning electron microscopy (VPSEM), transmission electron microscopy (TEM), Fourier transmission infrared spectroscopy (FT-IR), X-ray diffraction spectroscopy (XRD), and energy dispersive X-ray analyser (EDX). The reproducibility and low cost of the method suggested that it could be used in industry for the large scale synthesis of aragonite nanoparticles from cockle shells, a low cost and easily available natural resource.

Effect of using polyimide capillaries during thermal experiments on the particle size distribution of supported Pt nanoparticles

2015 ◽  
Vol 48 (5) ◽  
pp. 1599-1603 ◽  
Author(s):  
Liliana Gámez-Mendoza ◽  
Oscar Resto ◽  
María Martínez-Iñesta
Keyword(s):  
Electron Microscopy ◽  
Thermal Stability ◽  
Transmission Electron Microscopy ◽  
Low Cost ◽  
Pt Nanoparticles ◽  
Dark Field ◽  
High Angle ◽  
X Ray ◽  
Transmission Electron ◽  
Annular Dark Field

Kapton HN-type polyimide capillaries are commonly used as sample holders for transmission X-ray experiments at temperatures below 673 K because of their thermal stability, high X-ray transmittance and low cost. Using high-angle annular dark field scanning high-resolution transmission electron microscopy and thermogravimetric analysis, this work shows that using polyimide capillaries leads to the overgrowth of supported Pt nanoparticles during reduction at temperatures below the glass transition temperature (Tg= 658 K) owing to an outgassing of water from the polyimide. Quartz capillaries were also studied and this overgrowth was not observed.

Facile Synthesis and Electrical Conductivity of Carbon Nanotube Reinforced Nanosilver Composite

2012 ◽  
Vol 67 (12) ◽  
pp. 679-684 ◽  
Author(s):  
Hemant Pal ◽  
Vimal Sharma ◽  
Rajesh Kumar ◽  
Nagesh Thakur
Keyword(s):  
Electron Microscopy ◽  
Electrical Conductivity ◽  
Industrial Applications ◽  
X Ray Diffraction ◽  
Metal Matrix Nanocomposites ◽  
X Ray ◽  
Transmission Electron ◽  
Silver Matrix ◽  
Mixing Method ◽  
Matrix Nanocomposites

Metal matrix nanocomposites reinforced with carbon nanotubes (CNTs) have become popular in industrial applications. Due to their excellent thermophysical and mechanical properties, CNTs are considered as attractive filler for the improvement in properties of metals. In the present work, we have synthesized noncovalently functionalized CNT reinforced nanosilver composites by using a modified molecular level mixing method. The structure and morphology of nanocomposites are characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and energy dispersive spectroscopy. The electrical conductivity of silver-CNT nanocomposites measured by the four-point probe method is found to be more than that of the pure nanosilver. The significant improvement in electrical conductivity of Ag=CNT nanocomposites stems from homogenous and embedded distribution of CNTs in a silver matrix with intact structure resulting from noncovalent functionalization. The low temperature sintering also enhances the electrical conductivity of Ag=CNT nanocomposites.

scholarly journals Assessment of Ag Nanoparticles Interaction over Low-Cost Mesoporous Silica in Deep Desulfurization of Diesel

Catalysts ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 651 ◽  
Author(s):  
Rafael V. Sales ◽  
Heloise O. M. A. Moura ◽  
Anne B. F. Câmara ◽  
Enrique Rodríguez-Castellón ◽  
José A. B. Silva ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Ag Nanoparticles ◽  
Low Cost ◽  
Sulfur Compounds ◽  
Organosulfur Compounds ◽  
Regeneration Rate ◽  
X Ray ◽  
Transmission Electron ◽  
Sulfur Adsorption

Chemical interactions between metal particles (Ag or Ni) dispersed in a low-cost MCM-41M produced from beach sand amorphous silica and sulfur compounds were evaluated in the deep adsorptive desulfurization process of real diesel fuel. N2 adsorption-desorption isotherms, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HRTEM) and scanning transmission electron microscopy coupled to energy-dispersive X-ray spectroscopy (STEM-EDX) were used for characterizing the adsorbents. HRTEM and XPS confirmed the high dispersion of Ag nanoparticles on the MCM-41 surface, and its chemical interaction with support and sulfur compounds by diverse mechanisms such as π-complexation and oxidation. Thermodynamic tests indicated that the adsorption of sulfur compounds over Ag(I)/MCM-41M is an endothermic process under the studied conditions. The magnitude of ΔH° (42.1 kJ/mol) indicates that chemisorptive mechanisms govern the sulfur removal. The best fit of kinetic and equilibrium data to pseudo-second order (R2 > 0.99) and Langmuir models (R2 > 0.98), respectively, along with the results for intraparticle diffusion and Boyd’s film-diffusion kinetic models, suggest that the chemisorptive interaction between organosulfur compounds and Ag nanosites controls sulfur adsorption, as seen in the XPS results. Its adsorption capacity (qm = 31.25 mgS/g) was 10 times higher than that obtained for pure MCM-41M and double the qm for the Ag(I)/MCM-41C adsorbent from commercial silica. Saturated adsorbents presented a satisfactory regeneration rate after a total of five sulfur adsorption cycles.

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