Structural, Microscopy Analysis and Compressive Strength of ZnO–CuO Nanocomposites

2020 ◽  
Vol 12 (2) ◽  
pp. 163-167
Author(s):  
K. Kavitha ◽  
T. Subba Rao ◽  
R. Padma Suvarna ◽  
M. Prasanna Kumar

Currently, researches on nanocomposites become an active research area due its unique properties. Earlier, many researches are done for synthesizing the multidimensional structures for developing efficient and new Nano devices. In this present work, we synthesized ZnO–CuO nanocomposites using sol–gel method. The obtained nanocomposites were characterized by X-ray diffraction (XRD), transmission electron microscope (TEM) analysis and Compressive strength analysis using compressive testing machine (CTM). Herein, the structure and size of the ZnO–CuO nanocomposites were studied using XRD. And the average particle size was found to be 34 nm. The TEM analysis has the evidence of the XRD result. The enhancement in compressive strength of the ZnO–CuO nanocomposites was determined using CTM machine up to 4 wt.%.


2016 ◽  
Vol 709 ◽  
pp. 66-69
Author(s):  
Jeyashelly Andas ◽  
Rahmah Atikah Rosdi ◽  
Nur Izzati Mohd Anuar

A series of Fe-Co nanoparticles were synthesized via sol-gel route at acidic, neutral and basic condition using rice husk as the silica source. The synthesized nanomaterials were designated as Fe-Co3, Fe-Co7 and Fe-Co9 and characterized by Fourier Transform Infrared (FTIR), Transmission Electron Microscope (TEM) and particle size analyzer. The great effect of pH was clearly evidenced from the shifting in the siloxane bond in the FTIR spectrum. TEM investigation confirmed the existence of discrete and almost sphere like nanoparticles. The particle size decreased with an increase in the pH, registering the smallest average particle size at pH 9. In brief, this study promises a fast, rapid and promising method for the conversion of silica rice husk into nanoscale bimetallic materials.



2014 ◽  
Vol 900 ◽  
pp. 187-190
Author(s):  
Zong Hu Xiao ◽  
Wei Zhong ◽  
Kang Ping Xu ◽  
Yong Huang ◽  
Shui Gen Li ◽  
...  

Terbium-doped zinc oxide (ZnO:Tb) nanocrystals were prepared by a direct reactive precipitation progress. Incorporation of terbium in ZnO nanocrystals had been proved by X-ray diffraction (XRD), transmission electron microscope (TEM) and fluorescence spectrophotometer. XRD investigations confirm that the samples of ZnO:Tb nanocrystals with a hexagonal wurtzite crystalline structure don’t exist the diffraction peaks of the compounds of terbium. The results of TEM analysis show that the as-prepared samples with an average particle size less than 20 nm were obtained. The photoluminescence (PL) spectra suggest that there is no luminescence peaks corresponding to the terbium compounds in ZnO:Tb samples; the green emission intensity gradually decreases with the increase of the Tb-doped concentration in ZnO matrix. A core-shell model of rare earth (RE) passivated ZnO is proposed, which the passivation layer existing on the ZnO surface, can generate a barrier to impede the formation of oxygen vacancy, corresponding to the green emission.



2012 ◽  
Vol 15 (2) ◽  
pp. 27-34
Author(s):  
Nguyet Thi Thuy Dao ◽  
Duong Phuc Nguyen ◽  
Hien Duc Than

This paper presents the synthesis and characterization of Y3Fe5O12, Gd3Fe5O12 and Dy3Fe5O12 nanoparticles by sol-gel method using initial salts solution of Y(NO3)3, Gd(NO3)3, Dy(NO3)3, Fe(NO3). The lattice constant, crystallite size and particle morphology of these ferrite garnet nanoparticles were studied by using X-ray diffraction and transmission electron microscopy (TEM). The results showed that the garnet samples prepared by this method were formed at 800oC, which is lower than the sintering temperature for ceramic bulk samples (1400oC). The particle size is in the range 25- 40 nm as observed via TEM image and the average particle size was found to be 37nm using Debye- Scherrer formula.



2010 ◽  
Vol 2010 ◽  
pp. 1-6 ◽  
Author(s):  
Mehrdad Balandeh ◽  
Sirous Asgari

LiNiO2powders were synthesized with acrylic acid, citric acid, oxalic acid, and triethanolamine (TEA) as a chelating agent. CrystallizedLiNiO2was synthesized in air at a calcinations temperature of 500∘Cfor 12 hours, when the molar ratio of chelating agents to total metal ion (RPM) was 1.0. The TEA-assisted method had the highest intensity ratio of (003)/(104) peaks of X-ray diffraction (XRD) spectrum. The transmission electron microscopy (TEM) analysis indicates that the sample prepared with triethanolamine obtained the smallest particle size with average particle size of only 12 nm. The results indicate that chelating agents have an important role in the intensity ratio of (003)/(104) peaks of XRD spectrum, size and shape of powders.



2004 ◽  
Vol 12 (1) ◽  
pp. 30-33
Author(s):  
Paul Beauregard

Historically, one of the first jobs performed by the new instrument called a “transmission electron microscope” (TEM) was the determination of particle size and distribution. Particle size is still important in controlling the properties of sub-micron and nanoparticle products. The width and average particle size can determine the light scattering properties of a pigment like TiO2, for example. The cost of installing a TEM facility and TEM sample preparation issues makes TEM analysis expensive and labor intensive. So decades ago, nitrogen BET (Brunauer, Emmett, and Teller) surface area determinations were used on sub-micron powders and pigments to minimize these costs. The BET measurement of the exposed external surface area of a material is made by detecting and measuring the amount of nitrogen given off after absorption, assuming one atomic layer of nitrogen is adsorbed.



2006 ◽  
Vol 05 (02n03) ◽  
pp. 351-357 ◽  
Author(s):  
YOUNG SOO KANG ◽  
DONG RI ZHANG

Nanoparticles of titanium dioxide ( TiO 2) doped with 5 at.% Sc 3+ ions were synthesized using the sol–gel method and calcined at 500°C to obtain better anatase phase. The crystal structures of the doped TiO 2 nanoparticles were characterized by X-ray powder diffraction (XRD), Raman, UV-vis, FT-IR spectroscopy, high resolution transmission electron microscopy (HRTEM) and selected-area electron diffraction (SAED). XRD patterns and Raman spectra of TiO 2 + 5 at.% Sc -500°C show the anatase phase and the average particle size of the sample calculated from XRD patterns was determined as 5.9 nm. Well-resolved rings of SAED of TiO 2 doped with Sc 3+ ions are easily indexed to those from XRD pattern. HRTEM shows the well-defined lattice fringes and the lattice spacing measured from HRTEM is 0.33 nm, which is in well agreement with the distance between the (101) planes in anatase TiO 2. Energy-dispersive X-ray (EDX) spectrum of the doped TiO 2 confirms the presence of Sc element in the TiO 2 matrix.



Nanomaterials ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 2066
Author(s):  
Yu-Tai Shih ◽  
Yu-Ching Tsai ◽  
Der-Yu Lin

In this paper, the synthesis and characterization of CuIn1−xGaxSe2 (0 ≤ x ≤ 1) nanocrystals are reported with the influences of x value on the structural, morphological, and optical properties of the nanocrystals. The X-ray diffraction (XRD) results showed that the nanocrystals were of chalcopyrite structure with particle size in the range of 11.5–17.4 nm. Their lattice constants decreased with increasing Ga content. Thus, the x value of the CuIn1−xGaxSe2 nanocrystals was estimated by Vegard’s law. Transmission electron microscopy (TEM) analysis revealed that the average particle size of the nanocrystals agreed with the results of XRD. Well-defined lattice fringes were shown in the TEM images. An analysis of the absorption spectra indicated that the band gap energy of these CuIn1−xGaxSe2 nanocrystals was tuned from 1.11 to 1.72 eV by varying the x value from 0 to 1. The Raman spectra indicated that the A1 optical vibrational mode of the nanocrystals gradually shifted to higher wavenumber with increasing x value. A simple theoretical equation for the A1 mode frequency was proposed. The plot of this equation showed the same trend as the experimental data.



2012 ◽  
Vol 476-478 ◽  
pp. 1138-1141
Author(s):  
Zhi Qiang Wei ◽  
Qiang Wei ◽  
Li Gang Liu ◽  
Hua Yang ◽  
Xiao Juan Wu

Ag nanoparticles were successfully synthesized by hydrothermal method under the polyol system combined with traces of sodium chloride, Silver nitrate(AgNO3) and polyvinylpyrrolidone (PVP) acted as the silver source and dispersant respectively. The samples by this process were characterized via X-ray powder diffraction (XRD), Brunauer–Emmett–Teller (BET) adsorption equation, transmission electron microscopy (TEM) and the corresponding selected area electron diffraction (SAED) to determine the chemical composition, particle size, crystal structure and morphology. The experiment results indicate that the crystal structure of the samples is face centered cubic (FCC) structure as same as the bulk materials, The specific surface area is 24 m2/g, the particle size distribution ranging from10 to 50 nm, with an average particle size about 26 nm obtained by TEM and confirmed by XRD and BET results.



Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 808
Author(s):  
Ahmed Al Saqr ◽  
El-Sayed Khafagy ◽  
Ahmed Alalaiwe ◽  
Mohammed F. Aldawsari ◽  
Saad M. Alshahrani ◽  
...  

Green synthesis of gold nanoparticles (GNPs) with plant extracts has gained considerable interest in the field of biomedicine. Recently, the bioreduction nature of herbal extracts has helped to synthesize spherical GNPs of different potential from gold salt. In this study, a fast ecofriendly method was adopted for the synthesis of GNPs using fresh peel (aqueous) extracts of Benincasa hispida, which acted as reducing and stabilizing agents. The biosynthesized GNPs were characterized by UV–VIS and Fourier transform infrared spectroscopy, transmission electron microscopy (TEM), and dynamic light scattering. In addition, the in vitro antibacterial and anticancer activities of synthesized GNPs were investigated. The formation of gold nanoparticles was confirmed by the existence of a sharp absorption peak at 520 nm, corresponding to the surface plasmon resonance (SPR) band of the GNPs. TEM analysis revealed that the prepared GNPs were spherical in shape and had an average particle size of 22.18 ± 2 nm. Most importantly, the synthesized GNPs exhibited considerable antibacterial activity against different Gram-positive and Gram-negative bacteria. Furthermore, the biosynthesized GNPs exerted remarkable in vitro cytotoxicity against human cervical cancer cell line, while sparing normal human primary osteoblast cells. Such cytotoxic effect was attributed to the increased production of reactive oxygen species (ROS) that contributed to the damage of HeLa cells. Collectively, peel extracts of B. hispida can be efficiently used for the synthesis of GNPs, which can be adopted as a natural source of antimicrobial and anticancer agent.



2016 ◽  
Vol 15 (05n06) ◽  
pp. 1660002 ◽  
Author(s):  
V. Kavitha ◽  
P. S. Ramesh ◽  
D. Geetha

Copper doped Titanium dioxide TiO2 nanoparticles were synthesized by sol–gel method using titanium tetraisopropoxide and copper sulfate as precursors. The synthesized nanoparticles were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Scanning electron microscopy (SEM), UV-Visible spectroscopy (UV-Vis), Photoluminesce spectroscopy (PL) and atomic force microscopy (AFM). XRD analysis confirms the formation of anatase titanium dioxide and average particle size was 35[Formula: see text]nm. Cu– TiO2 exhibits a shift in the absorption edge toward visible spectrum. The rate of recombination and transfer behavior of the photoexcited electron–hole pairs in the semiconductors was recorded by photoluminescence. From SEM spherical shaped nanoparticles was observed. Comparing with pure TiO2 nanoparticles, Cu doped TiO2 photocatalyst exhibited enhanced photocatalytic activity under natural sunlight irradiation in the decomposition of rhodamine B aqueous solution. The maximum 97% of degradation efficiency of Rhodamine B was observed at 0.6% Cu–TiO2 within 180[Formula: see text]min. The photocatalytic efficiency of Rhodamine B of Cu doped TiO2 nanoparticle was higher than the pure TiO2, which could be attributed to the small crystallinity intense light absorption in Sunlight and narrow bandgap energy of Copper.



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