Synthesis and Electromagnetic Properties of Hollow Ceramic Microspheres

2011 ◽  
Vol 492 ◽  
pp. 260-263 ◽  
Author(s):  
Bao Cai Xu ◽  
Jian Jiang Wang ◽  
Rong Xia Duan ◽  
Xing Jian Huo

The hollow ceramic microspheres were prepared by Self-reactive flame spraying method. The structural characteristics and morphology properties of the composite powders were obtained by XRD and SEM. The results show that the obtained particles are hollow ceramic microspheres. The average particle size is about 30μm. An analytical method for the determination of electromagnetic parameters (ε, μ) of materials under test is presented by the analysis of normalized general matrix of equivalent network of coaxial line filled with samples. The analysis of vector network analyzer show that reflectance of hollow composite microspheres could well absorb microwaves in 2-18 GHz. The reflection loss is less than -l0dB in the range of 12.4 to15.2GHz while the minimum reflection loss is -18.5dB at 13.6GHz.

2002 ◽  
Vol 721 ◽  
Author(s):  
Monica Sorescu

AbstractWe propose a two-lattice method for direct determination of the recoilless fraction using a single room-temperature transmission Mössbauer measurement. The method is first demonstrated for the case of iron and metallic glass two-foil system and is next generalized for the case of physical mixtures of two powders. We further apply this method to determine the recoilless fraction of hematite and magnetite particles. Finally, we provide direct measurement of the recoilless fraction in nanohematite and nanomagnetite with an average particle size of 19 nm.


2020 ◽  
Vol 989 ◽  
pp. 199-203
Author(s):  
Ivan N. Egorov ◽  
Nikolay Ya. Egorov ◽  
Viktor P. Kryzhanovsky

The paper presents the results of experimental studies of strontium hexa-ferrite average particle size and structural characteristics changes during milling process. Coarse strontium hexaferrite was milled in beater mill, without and with electromagnetic effect. Electromagnetic effect was produced by constant and alternating gradient magnetic fields with mutually perpendicular induction lines. Particle sizes were measured by microscopic methods, and structural characteristics were calculated by processing of X-ray diffractograms. Diffraction studies showed that during milling process, both with and without electromagnetic effect, the most intensive changes of coherent scattering region (CSR) sizes, dislocation densities and relative deformation of particulate material occur at earlier stage of milling. At this stage the speed of average particle size decrease is maximal. At later stage both average particle size and structural characteristic changes correlate and have asymptotic character.


In this study, by taking the advantage of the facile & controlled synthesis of furosemide derived gold nanoparticles (Fr-AuNps) for rapid and sensitive amperometric determination of dopamine (DP). The one-step synthesis of FrAuNps was carried out at room temperature without the use of strong reducing agents. The synthesized Fr-AuNps were studied by UV-Vis spectroscopy, and a strong absorption band for gold nanoparticles was observed at 520 nm. Transmission electron micrographs (TEM) revealed the average particle size below 100 nm. HRTEM showed excellent crystalline features as prepared gold nanoparticles. The electrochemical behavior of gold nanoparticles was examined by cyclic voltammetry (CV) which demonstrated the enhanced electrocatalytic kinetics activity towards the oxidation of dopamine. The presented dopamine biosensor exhibited a linear response for the dopamine in the range of 0.25 to 7 µM. The calculated the detection limit found to be 18.3 nM and limit of quantification 61.5 nM respectively. The proposed dopamine biosensor was successfully employed for the quantification of trace amount of dopamine from human serum and the obtained results are very satisfactory.


2021 ◽  
Author(s):  
Nelli Maksymovych ◽  
Ludmila Oleksenko ◽  
George Fedorenko

The paper is devoted for a solution of indoors fires prevention at early stage by determination of H2 (fire precursor gas) in air using a semiconductor sensor. A material based on Pt-containing nanosized tin dioxide with an average particle size of 10–11 nm obtained via a sol–gel method was created for a gas sensitive layer of the sensor. The developed sensor has high sensitivity to H2 micro concentration, a wide range of its detectable content in air, selectivity of H2 measuring in the presence of СО and СН4, good dynamic properties. The combination of these properties is very important for prevention of inflammations on their early stages before the open fires appearance. Economic benefit of the proposed sensor is due to a lower cost and higher reliability of the fire situation detection.


1961 ◽  
Vol 34 (2) ◽  
pp. 433-445 ◽  
Author(s):  
E. Schmidt ◽  
P. H. Biddison

Abstract Knowledge of mass distribution of particle sizes in latex is very important to the latex technologist. Therefore, it is desirable to have available a simple method for the determination of mass distribution of particle sizes. This paper presents a method, based on fractional creaming of latex with sodium alginate, which can be used in any laboratory without special equipment. The method is particularly advantageous for analyzing latexes of very wide particle size distributions. When analyzed with an electron microscope, these latexes require counting a very large number of particles. McGavack found that partial creaming of normal hevea latex with ammonium alginate gives concentrates of larger average particle size than the original latex. He found that the average particle size in the cream approaches that of the original latex as the amount of creaming agent is increased. In a previous paper from this laboratory, Schmidt and Kelsey demonstrated that the phenomenon of fractionation according to particle size with increasing amounts of creaming agent is applicable in a wide variety of anionic latex systems and in colloidal silica. Their results indicated also the existence of a quantitative relationship, independent of the nature of the dispersed particles, between the concentration of creaming agent and size of creamed particles. Maron confirmed fractionation with respect to particle size as a consequence of partial creaming with alginate. He showed that the mass average particle sizes of fractions, determined optically, cumulate to that of the original latex. Although the previous paper by Schmidt and Kelsey implied the basic concept of a method of determining particle size distribution by fractional creaming, it was not exploited at that time. In order to adapt the fractional creaming phenomenon to a quantitative method for particle size determination, we required a more precise knowledge of the relation between creaming agent concentration and size of particles creamed. It was proposed to establish this relationship with the aid of the electron microscope. Various factors influencing the creaming of latex, such as polymer concentration, electrolyte, soap content, and variability of the creaming agent, had to be considered in standardizing the creaming procedure.


Coatings ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 848
Author(s):  
Aída Serrano ◽  
Jesús López-Sánchez ◽  
Iciar Arnay ◽  
Rosalía Cid ◽  
María Vila ◽  
...  

In this work, the functional character of complex α-Fe2O3(0001)/SrTiO3(111) and Au(111) islands/α-Fe2O3(0001)/SrTiO3(111) heterostructures has been proven as gas sensors at room temperature. Epitaxial Au islands and α-Fe2O3 thin film are grown by pulsed laser deposition on SrTiO3(111) substrates. Intrinsic parameters such as the composition, particle size and epitaxial character are investigated for their influence on the gas sensing response. Both Au and α-Fe2O3 layer show an island-type growth with an average particle size of 40 and 62 nm, respectively. The epitaxial and incommensurate growth is evidenced, confirming a rotation of 30° between the in-plane crystallographic axes of α-Fe2O3(0001) structure and those of SrTiO3(111) substrate and between the in-plane crystallographic axes of Au(111) and those of α-Fe2O3(0001) structure. α-Fe2O3 is the only phase of iron oxide identified before and after its functionalization with Au nanoparticles. In addition, its structural characteristics are also preserved after Au deposition, with minor changes at short-range order. Conductance measurements of Au(111)/α-Fe2O3(0001)/SrTiO3(111) system show that the incorporation of epitaxial Au islands on top of the α-Fe2O3(0001) layer induces an enhancement of the gas-sensing activity of around 25% under CO and 35% under CH4 gas exposure, in comparison to a bare α-Fe2O3(0001) layer grown on SrTiO3(111) substrates. In addition, the response of the heterostructures to CO gas exposure is around 5–10% higher than to CH4 gas in each case.


2009 ◽  
Vol 3 (1-2) ◽  
pp. 33-38 ◽  
Author(s):  
Songhak Yoon ◽  
Jürgen Dornseiffer ◽  
Detlev Hennings ◽  
Christian Pithan ◽  
Rainer Waser

BaTiO3 - Ag composite nanopowders were synthesized via microemulsion mediated synthesis through the hydrolytic decomposition of mixed metal alkoxide solutions as precursor for the BaTiO3 and the reduction of silver nitrate in the presence of polyvinylpyrrolidone (PVP) as source for the Ag nanoparticles. The X-ray diffraction (XRD) patterns indicate that BaTiO3 and Ag phases were successfully synthesized in the composite powders. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) show that the synthesized BaTiO3 nanoparticles were aggregates of nanosized primary particles as small as 10 nm in diameter and the average particle size of nanocrystalline Ag was about 100 nm. Calcination and sintering studies reveal that there exists a difference in the sintering behaviour of BaTiO3 and Ag in the composite nanopowders. Thermogravimetric analysis (TGA) shows weight losses due to the burnout of organic residues arising from the synthesis, the release of water from the surface and separation of hydroxyl ions from the lattice of BaTiO3 nanoparticles. A dilatometric study of BaTiO3-Ag composite confirmed a strong difference in the shrinkage behaviour compared to that of the pure BaTiO3 obtained by microemulsion mediated synthesis. .


2019 ◽  
Vol 8 (4) ◽  
pp. 6195-6197

In this study the intermetallic-matrix composite powders CoNiCrAlY-2wt. %Al2O3 were characterized in order to investigate the effect of heat exposure time on morphologies, grain growth and phases formed by facile suspension route synthesis. The as-synthesized powders were examined by Scanning Electron Microscopy (SEM), Energy Dispersive X-ray (EDX) and X-ray diffraction (XRD). The formation of NiAl phase was noticed after 1 hour of heat treatment. The average particle size of intermetallic-matrix composite powders CoNiCrAlY-2wt.%Al2O3 increased as the heat exposure time increased. It is found that the reinforcement of alumina allowed the particles to uniformly distributed when the sample was heated for 10 hours. The formation of NiAl started when the sample was heated at 1 hour and NiAl continued to form when heated at 10 hours.


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