scholarly journals Preparation, Properties, and Microbial Impact of Tungsten (VI) Oxide and Zinc (II) Oxide Nanoparticles Enriched Polyethylene Sebacate Nanocomposites

Polymers ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 718
Author(s):  
Amr S. Ismail ◽  
Salah M. Tawfik ◽  
Amr H. Mady ◽  
Yong-Ill Lee
Keyword(s):  
Electron Microscopy ◽  
Pathogenic Bacteria ◽  
Average Molecular Weight ◽  
Gel Permeation Chromatography ◽  
Polymerization Reaction ◽  
Condensation Polymerization ◽  
X Ray Diffraction ◽  
Ion Interactions ◽  
Transmission Electron ◽  
Coprecipitation Process

Nanoparticles of tungsten oxide (WO3) and zinc oxide (ZnO) enriched polyethylene sebacate (PES) nanocomposites were prepared through the coprecipitation process and condensation polymerization reaction. The obtained nano-sized particles of WO3 and ZnO, PES, and nanocomposites (WO3-PES NC and ZnO-PES NC) were investigated. The average molecular weight of the cured PES was measured by employing the gel permeation chromatography (GPC) technique. Fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) spectra assured the formation of the polymeric nanocomposites.WO3 and ZnO nanoparticles supposed a condensed porous spherical phase found implanted in the polymer structure, as detected by scanning electron microscopy (SEM) and transmission electron microscopy (TEM) methods. These nano-scale systems achieved an electrical activity based on the conductive nanoparticles embedded matrix as a result of the ion–ion interactions. The microbial influence of the nanocomposites was examined against pathogenic bacteria; Pseudomonas aeruginosa,Escherichia Coli, Staphylococcus Aureus, and Bacillus subtilis, and Fungi; Aspergillus niger, and Candidaalbicans. Results exhibited that these nanocomposites have antimicrobial effects from moderate to slightly high on bacteria and high on fungi which was confirmed by a clear zone of inhibition. This study contributes to the design of reasonable composites to be under evaluation for their catalytic effect.

scholarly journals SYNTHESIS OF NANO-ALUMINUM OXIDE VIA BIOLOGICAL AND ELECTROCHEMICAL METHODS

2019 ◽  
Vol 29 (4) ◽  
pp. 67
Author(s):  
Barakat A. F. Kamel
Keyword(s):  
Electron Microscopy ◽  
Aluminum Oxide ◽  
Pathogenic Bacteria ◽  
Research Work ◽  
Alumina Nanoparticles ◽  
X Ray Diffraction ◽  
Force Microscopy ◽  
Atomic Force ◽  
Transmission Electron ◽  
Stable Particles

In this research work, the nanoparticles of aluminum oxide were synthesized by two ways. The first way is the biological by using (Pseudomonas aeruginosa) bacteria with a rate diameter (102.35) nm. The second way is the electrochemical with a rate diameter (62) nm. These nanoparticles were characterized by Atomic Force Microscopy (AFM), X-Ray diffraction technique (XRD), Transmission Electron Microscopy (TEM) and Scanninig Electron Microscopy (SEM). Alumina nanoparticles are thermodynamically stable particles over a wide temperature range . The biological activity of these nanoparticles toward different species of pathogenic bacteria (Staphylococcus aureus ) and (Pseudo monas) has been investigated. The results stated that the nanoparticles prepared by chemical way was more effective on the inhibition of bacteria than the nanoparticles prepared by biological way

A linear polycarbosilane containing m-carborane units: Synthesis and characterization as precursor for SiC/B4C ceramics

2017 ◽  
Vol 30 (10) ◽  
pp. 1267-1275 ◽  
Author(s):  
Quan Zhou ◽  
Zhengqiang Peng ◽  
Mingze Yang ◽  
Hao Hu ◽  
Ning Song ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
High Temperature ◽  
Gel Permeation Chromatography ◽  
Inert Atmosphere ◽  
Composite Ceramics ◽  
X Ray Diffraction ◽  
Metathesis Reaction ◽  
X Ray ◽  
Air Atmosphere ◽  
Transmission Electron

The precursor of poly(carborane)(silicon-acetylene) (PCBS) for silicon carbide (SiC)/B4C composite ceramics was synthesized by a salt metathesis reaction. The molecular weight of PCBS was measured by gel permeation chromatography and the corresponding structures were identified by Fourier transform infrared (FTIR) spectroscopy and nuclear magnetic resonance (NMR). After thermal curing, the PCBS was converted to a dark red brittle nonporous monolith and the thermal stability was significantly improved, especially in an air atmosphere. Thermogravimetric analysis indicated that the 5% weight loss temperatures were 595°C and 633°C under nitrogen and air atmospheres, respectively, and the corresponding residues at 1000°C were 86.42% and 90.42%. After a heat treatment at 1600°C under inert atmosphere, the well-dispersed SiC/B4C ceramic was obtained and characterized by FTIR, X-ray diffraction analysis, Raman spectroscopy, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The obtained SiC/B4C ceramic has a good high-temperature and oxidation resistance which can be applied to aviation, aerospace, and other ultra-high temperature conditions.

scholarly journals Effect of Various Temperatures on Bletillae Rhizoma Polysaccharide Extraction and Physicochemical Properties

2018 ◽  
Vol 9 (1) ◽  
pp. 116 ◽  
Author(s):  
Xiaoyan Long ◽  
Quan Yan ◽  
Linwei Peng ◽  
Xinyue Liu ◽  
Xuegang Luo
Keyword(s):  
Electron Microscopy ◽  
Molecular Weight ◽  
Average Molecular Weight ◽  
Gel Permeation Chromatography ◽  
Extraction Temperature ◽  
X Ray Diffraction ◽  
Simple Process ◽  
X Ray ◽  
Gel Permeation ◽  
Scanning Electron

Six fractional polysaccharides were prepared by water extraction and alcohol precipitation under controlled temperature from bletillae rhizoma, a traditional Chinese medicine. Based on this, yields of bletillae rhizome polysaccharides (RBPs) were obtained. The extracting temperature impacted the characteristics of the fractional polysaccharides. The fractional polysaccharides were characterized by glucomannan (GM) content, thermal stability, scanning electron microscopy (SEM), Fourier-transform infrared (FTIR) spectroscopy, gel permeation chromatography (GPC), and x-ray diffraction (XRD). For the analysis, 2.0% w/v dispersions of the six fractional polysaccharides were prepared and their flow behaviors were evaluated using a rotational rheometer. The results showed that increased extraction temperature led to increased GM extraction yields and extraction rate, but GM content was relative stable (over 90%). The average molecular weight (Mw) of fractional polysaccharides obtained at 30, 40, 50, 60, 70, and 80 °C was 3.598 × 104, 4.188 × 104, 8.632 × 104, 8.850 × 104, 2.372 × 105, and 3.081 × 105 g/mol, respectively. SEM revealed that fractional polysaccharides had a porous structure of different sizes and densities. Thermal analysis, FTIR, and XRD results indicated that extraction temperature affects the structure and moisture content of fractional polysaccharides. All results showed that the extraction temperature has an obvious impact on the morphology, molecular weight, and polydispersity of the RBPs. This simple process is a promising method for the preparation of fractional polysaccharides.

A High Resolution Study of G.P. Zones in Aluminum - 4.2 at % Silver

1982 ◽  
Vol 40 ◽  
pp. 722-723 ◽  
Author(s):  
R. Gronsky
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
High Resolution ◽  
Computer Simulations ◽  
Structural Characteristics ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Resolution Study

The phenomenon of clustering in Al-Ag alloys has been extensively studied since the early work of Guinierl, wherein the pre-precipitation state was characterized as an assembly of spherical, ordered, silver-rich G.P. zones. Subsequent x-ray and TEM investigations yielded results in general agreement with this model. However, serious discrepancies were later revealed by the detailed x-ray diffraction - based computer simulations of Gragg and Cohen, i.e., the silver-rich clusters were instead octahedral in shape and fully disordered, atleast below 170°C. The object of the present investigation is to examine directly the structural characteristics of G.P. zones in Al-Ag by high resolution transmission electron microscopy.

Identification of calcium oxalate crystals in dried or fixed tobacco leaf

1984 ◽  
Vol 42 ◽  
pp. 288-289
Author(s):  
Vicki L. Baliga ◽  
Mary Ellen Counts
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Calcium Oxalate ◽  
Growth And Development ◽  
Polarized Light ◽  
Calcium Oxalate Crystals ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

Calcium is an important element in the growth and development of plants and one form of calcium is calcium oxalate. Calcium oxalate has been found in leaf seed, stem material plant tissue culture, fungi and lichen using one or more of the following methods—polarized light microscopy (PLM), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and x-ray diffraction.Two methods are presented here for qualitatively estimating calcium oxalate in dried or fixed tobacco (Nicotiana) leaf from different stalk positions using PLM. SEM, coupled with energy dispersive x-ray spectrometry (EDS), and powder x-ray diffraction were used to verify that the crystals observed in the dried leaf with PLM were calcium oxalate.

Epitaxy and texture analysis of Bi-Sr-Ca-Cu-O thin films on (100) MgO using Transmission Electron Microscopy

1990 ◽  
Vol 48 (4) ◽  
pp. 68-69
Author(s):  
J. T. Sizemore ◽  
D. G. Schlom ◽  
Z. J. Chen ◽  
J. N. Eckstein ◽  
I. Bozovic ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Transmission Electron Microscopy ◽  
Critical Currents ◽  
Unit Cell ◽  
X Ray Diffraction ◽  
Cell Axis ◽  
Transmission Electron ◽  
Synthesis Procedure

Investigators observe large critical currents for superconducting thin films deposited epitaxially on single crystal substrates. The orientation of these films is often characterized by specifying the unit cell axis that is perpendicular to the substrate. This omits specifying the orientation of the other unit cell axes and grain boundary angles between grains of the thin film. Misorientation between grains of YBa2Cu3O7−δ decreases the critical current, even in those films that are c axis oriented. We presume that these results are similar for bismuth based superconductors and report the epitaxial orientations and textures observed in such films.Thin films of nominally Bi2Sr2CaCu2Ox were deposited on MgO using molecular beam epitaxy (MBE). These films were in situ grown (during growth oxygen was incorporated and the films were not oxygen post-annealed) and shuttering was used to encourage c axis growth. Other papers report the details of the synthesis procedure. The films were characterized using x-ray diffraction (XRD) and transmission electron microscopy (TEM).

Devitrification products of rapidly solidified Ni-Nb amorphous alloys.

1990 ◽  
Vol 48 (4) ◽  
pp. 950-951
Author(s):  
G. A. Bertero ◽  
W.H. Hofmeister ◽  
N.D. Evans ◽  
J.E. Wittig ◽  
R.J. Bayuzick
Keyword(s):  
Electron Microscopy ◽  
Amorphous Structure ◽  
Sulphuric Acid Solution ◽  
X Ray Diffraction ◽  
High Fracture ◽  
Transmission Electron ◽  
Xrd Techniques ◽  
Rapidly Solidified ◽  
Electromagnetically Levitated

Rapid solidification of Ni-Nb alloys promotes the formation of amorphous structure. Preliminary results indicate promising elastic properties and high fracture strength for the metallic glass. Knowledge of the thermal stability of the amorphus alloy and the changes in properties with temperature is therefore of prime importance. In this work rapidly solidified Ni-Nb alloys were analyzed with transmission electron microscopy (TEM) during in-situ heating experiments and after isothermal annealing of bulk samples. Differential thermal analysis (DTA), scanning electron microscopy (SEM) and x-ray diffraction (XRD) techniques were also used to characterize both the solidification and devitrification sequences.Samples of Ni-44 at.% Nb were electromagnetically levitated, melted, and rapidly solidified by splatquenching between two copper chill plates. The resulting samples were 100 to 200 μm thick discs of 2 to 3 cm diameter. TEM specimens were either ion-milled or alternatively electropolished in a methanol-10% sulphuric acid solution at 20 V and −40°C.

Defect morphology in thick relaxed layers of InGaAs on GaAs

1990 ◽  
Vol 48 (4) ◽  
pp. 668-669
Author(s):  
R H Dixon ◽  
P Kidd ◽  
P J Goodhew
Keyword(s):  
Electron Microscopy ◽  
Surface Morphology ◽  
Growth Conditions ◽  
X Ray Diffraction ◽  
Double Crystal ◽  
Strained Layers ◽  
Good Surface ◽  
Transmission Electron ◽  
Device Structures ◽  
Surface Morphologies

Thick relaxed InGaAs layers grown epitaxially on GaAs are potentially useful substrates for growing high indium percentage strained layers. It is important that these relaxed layers are defect free and have a good surface morphology for the subsequent growth of device structures.3μm relaxed layers of InxGa1-xAs were grown on semi - insulating GaAs substrates by Molecular Beam Epitaxy (MBE), where the indium composition ranged from x=0.1 to 1.0. The interface, bulk and surface of the layers have been examined in planar view and cross-section by Transmission Electron Microscopy (TEM). The surface morphologies have been characterised by Scanning Electron Microscopy (SEM), and the bulk lattice perfection of the layers assessed using Double Crystal X-ray Diffraction (DCXRD).The surface morphology has been found to correlate with the growth conditions, with the type of defects grown-in to the layer (e.g. stacking faults, microtwins), and with the nature and density of dislocations in the interface.

Synthesis of ZnO/ZnFe2O4 nanocomposites in organic-free media and their photocatalytic activity under natural sunlight

2020 ◽  
Vol 14 (2) ◽  
pp. 6801-6810
Author(s):  
Rahmayeni Rahmayeni ◽  
Zulhadjri Zulhadjri ◽  
Yeni Stiadi ◽  
Agusnar Harry ◽  
Syukri Arief
Keyword(s):  
Electron Microscopy ◽  
Hexagonal Wurtzite Structure ◽  
Rice Grain ◽  
X Ray Diffraction ◽  
Homogeneous Sphere ◽  
Natural Sunlight ◽  
Transmission Electron ◽  
Photocatalytic Activities ◽  
Free Media ◽  
Photocatalytic Applications

Nanocomposite ZnO/ZnFe2O4 photocatalysts with different proportions of ZnFe2O4 were synthesized in organic-free media using metal nitric as precursors. The ZnO phase with hexagonal wurtzite structure and low crystallinity of ZnFe2O4 was confirmed using XRD (X-Ray diffraction). Different morphologies of the nanocomposites were obtained ranging from rice grain-like with a porous surface to homogeneous sphere-like nanoparticles as shown in Scanning Electron Microscopy (SEM) and TEM Transmission Electron Microscopy (TEM) studies. Magnetic properties measured by Visible Sampler Magnetometer (VSM) showed diamagnetic and paramagnetic behavior for the nanocomposites. Analysis with Diffuse Reflectance Spectrophotometer (DRS) UV-vis showed an increase the composition of ferrite in composites increasing its ability to absorb visible light. Photocatalytic activities of ZnO/ZnFe2O4 nanocomposites on the degradation of Rhodamine B dye reached 95.6% after 3 h under natural sunlight suggesting their suitability for sunlight driven photocatalytic applications. 

The Effect of the Microstructure of Diffusion Barriers on the Palladium Activation for Electroless Copper Deposition

2002 ◽  
Vol 716 ◽  
Author(s):  
Seok Woo Hong ◽  
Yong Sun Lee ◽  
Ki-Chul Park ◽  
Jong-Wan Park
Keyword(s):  
Electron Microscopy ◽  
Diffusion Barriers ◽  
Copper Deposition ◽  
X Ray Diffraction ◽  
Plan View ◽  
X Ray ◽  
Transmission Electron ◽  
Electroless Copper ◽  
Sheet Resistance Measurement ◽  
Scanning Electron

AbstractThe effect of microstructure of dc magnetron sputtered TiN and TaN diffusion barriers on the palladium activation for autocatalytic electroless copper deposition has been investigated by using X-ray diffraction, sheet resistance measurement, field emission scanning electron microscopy (FE-SEM) and plan view transmission electron microscopy (TEM). The density of palladium nuclei on TaN diffusion barrier increases as the grain size of TaN films decreases, which was caused by increasing nitrogen content in TaN films. Plan view TEM results of TiN and TaN diffusiton barriers showed that palladium nuclei formed mainly on the grain boundaries of the diffusion barriers.

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