Preparation of PS@SiO2, PS@TiO2，PS@TiO2/SiO2 Core-Shell Composites by a Spray Drying Process and Their Hollow Spheres after Removing PS Cores by Calcinations

2011 ◽  
Vol 194-196 ◽  
pp. 389-392
Author(s):  
Ling Li ◽  
Hong Liang Li ◽  
Ying Chun Zhu ◽  
Ai Ping Fu ◽  
Yong Wan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Spray Drying ◽  
Hollow Spheres ◽  
Nitrogen Adsorption ◽  
Core Shell ◽  
Drying Process ◽  
The Core ◽  
Adsorption Desorption ◽  
Drying Chamber ◽  
Scanning Electron

Polystyrene (PS) spheres encapsulated core-shell composites of SiO2or TiO2nanoparticles were prepared by the spray drying technique and hollow spheres of SiO2or TiO2nanoparticles were then derived by removing the PS cores with calcinations. The PS spheres were dispersed into the SiO2or TiO2colloids, forming a suspension and then the suspensions were sprayed to form micrometer-sized droplets, as the droplets rush through the drying chamber, the PS spheres were encapsulated into the core of SiO2or TiO2particles due to the high temperatures and the instant evaporation, obtaining PS@SiO2, PS@TiO2or PS@SiO2/TiO2core-shell composites. After removing the PS core by calcination at 550°C, SiO2or TiO2hollow spheres were then derived. The influence of drying temperature, the concentration of the SiO2or TiO2particles and the ratio of PS sphere to the particles on the structures and specific surface area of the hollow spheres were studied with scanning electron microscopy (SEM) and nitrogen adsorption-desorption measurements.

Synthesis of Novel Core-Shell Structured Hydroxyapatite/Meso-Silica for Removal of Methylene Blue from Aqueous Solutions

2012 ◽  
Vol 463-464 ◽  
pp. 543-547 ◽  
Author(s):  
Cheng Feng Li ◽  
Xiao Lu Ge ◽  
Shu Guang Liu ◽  
Fei Yu Liu
Keyword(s):  
Methylene Blue ◽  
Aqueous Solutions ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Low Cost ◽  
Nitrogen Adsorption ◽  
Precipitation Method ◽  
Core Shell ◽  
Adsorption Desorption

Core-shell structured hydroxyapatite (HA)/meso-silica was prepared and used as absorbance of methylene blue (MB). HA/meso-silica was synthesized in three steps: preparation of nano-sized HA by wet precipitation method, coating of dense silica and deposition of meso-silica shell on HA. As-received samples were characterized by Fourier transformed infare spectra, small angle X-ray diffraction, nitrogen adsorption-desorption isotherm and transmission electron microscopy. A wormhole framework mesostructure was found for HA/meso-silica. The specific surface area and pore volume were 128 m2•g-1 and 0.36 cm3•g-1, respectively. From the adsorption isotherm, HA/meso-silica with the great specific surface area exhibited a prominent adsorption capacity of MB (134.0 mg/g) in comparison with bare HA (0 mg/g). This study might shed light on surface modification of conventional low-cost adsorbents for removal of organic pollutants from aqueous solutions.

scholarly journals Synthesis and Control of the Shell Thickness of Polyaniline and Polypyrrole Half Hollow Spheres Using the Polystyrene Cores

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Su-Ryeon Yun ◽  
Gyeong-Ok Kim ◽  
Chan Woo Lee ◽  
Nam-Ju Jo ◽  
Yongku Kang ◽  
...  
Keyword(s):  
Shell Thickness ◽  
Hollow Spheres ◽  
Core Shell ◽  
Chemical Structures ◽  
The Core ◽  
Vis Spectroscopy ◽  
Ft Ir ◽  
Core Shell Structure ◽  
And Control ◽  
Ft Ir Spectroscopy

Polyaniline (Pani) and polypyrrole (Ppy) half hollow spheres with different shell thicknesses were successfully synthesized by three steps process using polystyrene (PS) as the core. The PS core was synthesized by emulsion polymerization. Aniline and pyrrole monomers were polymerized on the surface of the PS core. The shells of Pani and Ppy were fabricated by adding different amounts of aniline and pyrrole monomers. PS cores were dissolved and removed from the core shell structure by solvent extraction. The thicknesses of the Pani and Ppy half hollow spheres were observed by FE-SEM and FE-TEM. The chemical structures of the Pani and Ppy half hollow spheres were characterized by FT-IR spectroscopy and UV-Vis spectroscopy. The shell thicknesses of the Pani half hollow spheres were 30.2, 38.0, 42.2, 48.2, and 52.4 nm, while the shell thicknesses of the Ppy half hollow spheres were 16.0, 22.0, 27.0, and 34.0 nm. The shell thicknesses of Pani and Ppy half hollow spheres linearly increased as the amount of the monomer increased. Therefore, the shell thickness of the Pani and Ppy half hollow spheres can be controlled in these ranges.

Environmental Scanning Electron Microscopy Technique to Identify Asbestos Phases Inside Ferruginous Bodies

2013 ◽  
Vol 19 (2) ◽  
pp. 420-424 ◽  
Author(s):  
Alessandro Croce ◽  
Maya Musa ◽  
Mario Allegrina ◽  
Paolo Trivero ◽  
Caterina Rinaudo
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Chemical Elements ◽  
Environmental Scanning Electron Microscopy ◽  
Environmental Scanning ◽  
Thin Sections ◽  
The Core ◽  
Microscopy Technique ◽  
Ferruginous Bodies ◽  
Scanning Electron

AbstractFerruginous bodies observed in lungs of patients affected by mesothelioma, asbestosis, and pulmonary carcinoma are important to relate the illness to exposure, environmental or occupational, to asbestos. Identification of the inorganic phase constituting the core of the ferruginous bodies, formed around asbestos but also around phases different from asbestos, is essential for legal purposes. Environmental scanning electron microscopy/energy dispersive spectroscopy was used to identify the fibrous mineral phase in the core of ferruginous bodies observed directly in thin sections of tissue, without digestion of the biological matrix. Spectra were taken with sequential analyses along a line crossing the core of the ferruginous bodies. By comparing the spectra taken near to and far from the core, the chemical elements that make up the core could be identified.

Formation of bismuth iron oxide based core–shell structures and their dielectric, ferroelectric and magnetic properties

2019 ◽  
Vol 7 (5) ◽  
pp. 1280-1291 ◽  
Author(s):  
Alaka Panda ◽  
R. Govindaraj ◽  
R. Mythili ◽  
G. Amarendra
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Magnetic Properties ◽  
Iron Oxide ◽  
Shell Structures ◽  
Core Shell ◽  
Bismuth Iron Oxide ◽  
The Core ◽  
Shell Nanostructures ◽  
Transmission Electron

Bismuth and iron oxides subjected to ball milling followed by controlled annealing treatments showed the formation of core–shell nanostructures with Bi2Fe4O9 as the core and a shell of BiFeO3 and Bi25FeO40 phases as deduced based on the analysis of transmission electron microscopy results.

Corrosion Behavior of Q235A Steel under Wet-Dry Cyclic Condition

2012 ◽  
Vol 557-559 ◽  
pp. 139-142
Author(s):  
Jian Guo Liu ◽  
Yan Tao Li ◽  
Bao Rong Hou
Keyword(s):  
Electron Microscopy ◽  
Chloride Concentration ◽  
Corrosion Products ◽  
Drying Process ◽  
X Ray Diffraction ◽  
Cathodic Process ◽  
X Ray ◽  
Reduction Processes ◽  
Cyclic Condition ◽  
Scanning Electron

The corrosion processes and mechanisms of Q235A steel under wet-dry cyclic condition were studied using polarization curve compared with immersion samples, while, the corrosion morphologies and corrosion products of the steel samples were characterized using scanning electron microscopy (SEM) and X-ray diffraction (XRD). The cathodic process of wet-dry samples was likely to be controlled not by the oxygen reduction, but rather by the reduction of corrosion products. During the drying process of the wet-dry sample, the electrolyte thickness decreased and chloride concentration increased. Oxygen would be much easier to diffuse into the interface of electrolyte/metal, which improved the cathodic reduction processes. Except for this, the rust itself took part in the reduction processes and hence increased the corrosion rate of the steel samples.

CORE-SHELL Zn/ZnO STRUCTURES WITH IMPROVED PHOTOCATALYTIC PROPERTIES SYNTHESIZED BY AQUEOUS SOLUTION METHOD

2013 ◽  
Vol 06 (06) ◽  
pp. 1350058 ◽  
Author(s):  
YUAN MING HUANG ◽  
QING-LAN MA ◽  
BAO-GAI ZHAI
Keyword(s):  
Aqueous Solution ◽  
Photocatalytic Activity ◽  
Solution Method ◽  
Core Shell ◽  
Green Method ◽  
X Ray ◽  
The Core ◽  
Semiconductor Junction ◽  
Aqueous Solution Method ◽  
Scanning Electron

A facile and green method was utilized to synthesize core-shelled Zn / ZnO microspheres by boiling Zn microparticles in water for improving the photocatalytic activity of ZnO . The synthesized Zn / ZnO core-shells were investigated by means of scanning electron microscope, X-ray diffractometer and photoluminescence spectrometer, respectively. The morphology analysis showed that the metallic Zn core was about 6 μm in diameter while the ZnO shell was about 600 nm in thickness. Compared to ZnO nanoparticles, the core-shelled Zn / ZnO microspheres exhibited improved photocatalytic activity in degrading methyl orange in water. Our results suggest that the metal–semiconductor junction formed at the Zn / ZnO interface is responsible for the enhanced photocatalytic activity of ZnO .

Morphological Investigation of Solute Particles Trapped from an Air-Acetylene Flame

1986 ◽  
Vol 40 (7) ◽  
pp. 939-944 ◽  
Author(s):  
A. G. Childers ◽  
G. M. Hieftje
Keyword(s):  
Electron Microscopy ◽  
Structural Changes ◽  
Hollow Spheres ◽  
Structure Characteristic ◽  
Morphological Investigation ◽  
Droplet Generator ◽  
Trapped Particles ◽  
Morphological Studies ◽  
Uniform Droplet ◽  
Scanning Electron

A uniform-droplet generator has been employed to produce individual desolvated KCl particles in a laminar air-acetylene flame. The resulting particles were collected on various surfaces and at different points in their vaporization history. Morphological studies were then conducted on the trapped particles in order to better characterize the structural changes which occur during desolvation and vaporization. Particles collected early in their vaporization exhibited strong crystalline structure characteristic of KCl, whereas particles gathered later in their volatilization history showed evidence of fusion and, in some cases, the formation of hollow spheres. In addition to the morphological studies, the various collection surfaces and the collection technique itself were assessed. Direct collection on scanning-electron microscopy specimen stubs was judged to be best.

scholarly journals Facile Preparation of g-C3N4-WO3 Composite Gas Sensing Materials with Enhanced Gas Sensing Selectivity to Acetone

2019 ◽  
Vol 2019 ◽  
pp. 1-8 ◽  
Author(s):  
Xiangfeng Chu ◽  
Junsong Liu ◽  
Shiming Liang ◽  
Linshan Bai ◽  
Yongping Dong ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Gas Sensing ◽  
Hydrothermal Processing ◽  
Optimum Temperature ◽  
X Ray ◽  
Gas Sensing Properties ◽  
Facile Preparation ◽  
Adsorption Desorption ◽  
Scanning Electron

In this paper, g-C3N4-WO3 composite materials were prepared by hydrothermal processing. The composites were characterized by means of X-ray powder diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and N2 adsorption-desorption, respectively. The gas sensing properties of the composites were investigated. The results indicated that the addition of appropriate amount of g-C3N4 to WO3 could improve the response and selectivity to acetone. The sensor based on 2 wt% g-C3N4-WO3 composite showed the best gas sensing performances. When operating at optimum temperature of 310°C, the responses to 1000 ppm and 0.5 ppm acetone were 58.2 and 1.6, respectively, and the ratio of the S1000 ppm acetone to S1000 ppm ethanol reached 3.7.

The Preparation and Characterization of Redispersible Polymer Powder with Core-Shell Structure

2013 ◽  
Vol 687 ◽  
pp. 88-93
Author(s):  
Jian Xu ◽  
Zhong Jun Feng ◽  
Le Feng Fu ◽  
Bai Cun Zheng
Keyword(s):  
Electron Microscopy ◽  
Spray Drying ◽  
Shell Morphology ◽  
Core Shell ◽  
Drying Methods ◽  
Seeded Emulsion Polymerization ◽  
Transition Electron Microscopy ◽  
Polymer Powder ◽  
Particle Size Analyzer ◽  
Redispersible Polymer Powder

Acrylate polymer emulsion was synthesized by semi-continuous seeded emulsion polymerization with methacrylic acid (MAA) as the hydrophilic shell monomer. The redispersible polymer powder was prepared by spray drying method. The effects of the amount of MAA, styrene (St) stoichiometry equivalents to methyl methacrylate, and two kinds of spray drying methods on size distribution of the redispersible polymer powder were further systematically investigated. The Malvern laser particle size analyzer, transition electron microscopy (TEM), scanning electron microscopy (SEM) and differential scanning calorimeter were employed to characterize the redispersible polymer powder. Results showed that the redispersible polymer powder obtained by pneumatic spray drying with excellent re-dispersibility could be synthesized at 10 % of MAA, 50 % of St stoichiometry equivalents. The final copolymer emulsion with “perfect” core-shell morphology was approved by TEM, and the comparable film forming ability of the redispersible polymer powder with the original emulsion was observed by SEM, which could form a dense and smooth membrane.

scholarly journals Preparation of BaZrO3 powders by a spray-drying process

2003 ◽  
Vol 18 (6) ◽  
pp. 1325-1332 ◽  
Author(s):  
B. Robertz ◽  
F. Boschini ◽  
A. Rulmont ◽  
R. Cloots ◽  
I. Vandriessche ◽  
...  
Keyword(s):  
Spray Drying ◽  
Precursor Solution ◽  
Barium Zirconate ◽  
Drying Process ◽  
X Ray Diffraction ◽  
High Quality ◽  
Corrosion Resistant ◽  
X Ray ◽  
Potential Use ◽  
Scanning Electron

The potential use of barium zirconate for the manufacture of corrosion-resistant substrates emphasizes the need for a simple, inexpensive, and easily scalable process to produce high-quality powders with well-controlled composition and properties. However, the classical solid-state preparation of barium zirconate leads to an inhomogeneous powder unsuitable for applications in highly corrosive environment. For this paper, the possibility to use the spray-drying technique for the preparation of BaZrO3 powders with a controlled size distribution and morphology was investigated. The influence of the nature and concentration of the precursor solution and the influence of the spray-drying step are discussed on the basis of x-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, and dilatometric measurements.

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