Structural Properties of Size Variation of Nanocrystallites

2015 ◽  
Vol 813-814 ◽  
pp. 226-229
Author(s):  
S. Chellamal ◽  
A.P. Karthikeyan ◽  
P. Harsha ◽  
S. Manivannan
Keyword(s):  
Size Variation ◽  
Diffraction Method ◽  
Cadmium Sulphide ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Morphological Studies ◽  
Microscopy Method ◽  
Average Size

Silver doped cadmium sulphide nanocrystallites (CdS:Ag), undoped cadmium sulphide nanocrystallites (CdS), have been synthesized by the chemical precipitation method. Nanocrystalline materials are confirmed by the scanning electron microscopy method. The presented elements are identified by EDAX (Energy Dispersive X-ray Analysis). X-ray diffraction Method (XRD) is used to calculate the average size of the prepared sample. Morphological studies (SEM) are used to analyse the nature of the sample. The results are reported in this paper.

Cadmium Sulphide Nanocrystallites for Optoelectronic Devices

2019 ◽  
Vol 969 ◽  
pp. 237-241
Author(s):  
R. Sivanand ◽  
S. Chellammal ◽  
S. Manivannan
Keyword(s):  
Diffraction Method ◽  
Cadmium Sulphide ◽  
Precipitation Method ◽  
Energy Dispersive Analysis ◽  
X Ray Diffraction ◽  
Visible Spectroscopy ◽  
X Ray ◽  
Morphological Studies ◽  
Scanning Electron Microscopy Measurement ◽  
Microscopy Measurement

Cadmium sulphide nanocrystallites have been synthesized using precipitation method. The average sizes of the prepared samples is determined by XRD (x-ray diffraction) method. Morphological studies are carried out by SEM (scanning electron microscopy) measurement. Necesssary elements present in prepared samples, are confirmed by EDAX (energy dispersive analysis of x-ray spectroscopy) method. By Ultraviolet visible spectroscopy measurement, the value of absorption wavelength, band gap values are calculated in optical method. The electrical properties are analysed using impedance analyser measurement for the Nanocrystallites.

Synthesis, Structural Analysis of Cadmium Sulphide Nanocrystallites

2019 ◽  
Vol 969 ◽  
pp. 169-174
Author(s):  
R. Sivanand ◽  
S. Chellammal ◽  
S. Manivannan
Keyword(s):  
Size Variation ◽  
Cadmium Sulphide ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
Precipitation Method ◽  
Capping Agent ◽  
Energy Dispersive Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

In this paper, the effect of size variation of cadmium sulphide nanocrystallites which have been prepared by precipitation method is analyzed. These prepared samples were studied using X-ray diffraction (XRD), Scanning electron microscopy (SEM), and Energy dispersive analysis of spectroscopy (EDAX) techniques. SEM analysis represents the morphological nature of prepared samples and EDAX indicates the confirmation of elements present in the sample. XRD analysis determines the size of the samples and identifies the structure using miller indices (h k l values) of the nanocrystallies matches with JCPDS. From the XRD analysis, the size variation which depends on dopant, capping agent are discussed and corresponding results are reported in this paper.

scholarly journals Application of Copper doped Cadmium Sulphide Nanocrystallites for controlling Oral Pathogen activity

2020 ◽  
Vol 9 (3) ◽  
pp. 1324-1327
Keyword(s):  
Micrococcus Luteus ◽  
Shigella Flexneri ◽  
Diffraction Method ◽  
Cadmium Sulphide ◽  
Antimicrobial Action ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Oral Pathogens ◽  
Co Precipitation

In this study, we tend to incontestable the synthesis and antimicrobial action of Copper doped Cadmium Sulphide nanomaterials averse oral pathogens.Using Chemical Co-Precipitation method, Copper doped cadmium sulphide (Cu:CdS) nanomaterials are Synthesised. The sizes of the samples prepared are found by XRD (x-ray diffraction) method. SEM (scanning electron microscopy carried out to find the Morphological analysis. Materials present are confirmed by EDAX (energy dispersive analysis of x-ray spectroscopy) method. The outcomes showed that the proteins, which contain amine gatherings, played a diminishing and controlling obligation during the arrangement of Copper doped cadmium sulphide (Cu:CdS) nanomaterials in the colloidal arrangement. The antimicrobial action was evaluated against oral pathogens, for example, Bacillus subtilis, Micrococcus luteus, Staphylococcus aureus, Escherichia coli, Proteus vulgaris and Shigella flexneri and these outcomes affirmed that the Copper doped Cadmium sulphide nanomaterials are showing great bactericial action.

Synthesis and photocatalytic properties of magnetic separable and recyclable p-n heterojunction CoFe2O4/Bi12O17Cl2 photocatalyst

CrystEngComm ◽  
2021 ◽  
Author(s):  
Kexin Fang ◽  
Lei Shi ◽  
Lishuang Cui ◽  
Chunwei Shi ◽  
Weiwei Si
Keyword(s):  
Chemical Precipitation ◽  
Photocatalytic Properties ◽  
Chemical Precipitation Method ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
High Crystallinity

A series of CoFe2O4/Bi12O17Cl2 (CFO/Bi12O17Cl2) nanocomposites have been prepared by chemical precipitation method. The result of X-ray diffraction showed that CFO/Bi12O17Cl2 composites had high crystallinity. It was found that CoFe2O4...

Monodisperse Fe3O4/Fe Core/Shell Nanoparticles with Enhanced Magnetic Property

2011 ◽  
Vol 306-307 ◽  
pp. 410-415
Author(s):  
Li Sun ◽  
Fu Tian Liu ◽  
Qi Hui Jiang ◽  
Xiu Xiu Chen ◽  
Ping Yang
Keyword(s):  
Average Diameter ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
Core Shell ◽  
X Ray Diffraction ◽  
Shell Nanoparticles ◽  
X Ray ◽  
Transmission Electron ◽  
Shell Particles ◽  
Core Shell Nanoparticles

Core/shell type nanoparticles with an average diameter of 20nm were synthesized by chemical precipitation method. Firstly, Monodisperse Fe3O4 nanoparticles were synthesized by solvethermal method. FeSO4ž7H2O and NaBH4 were respectively dissolved in distilled water, then moderated Fe3O4 particles and surfactant(PVP) were ultrasonic dispersed into the FeSO4ž7H2O solution. The resulting solution was stirred 2 h at room temperature. Fe could be deposited on the surface of monodispersed Fe3O4 nanoparticles to form core-shell particles. The particles were characterized by using various experimental techniques, such as transmission electron microscopy (TEM), X-ray diffraction (XRD), AGM and DTA. The results suggest that the saturation magnetization of the nanocomposites is 100 emu/g. The composition of the samples show monodisperse and the sides of the core/shell nanoparticles are 20-30nm. It is noted that the formation of Fe3O4/Fe nanocomposites magnetite nanoparticles possess superparamagnetic property.

scholarly journals Crystal Chemistry and Luminescence Properties of Eu-Doped Polycrystalline Hydroxyapatite Synthesized by Chemical Precipitation at Room Temperature

Crystals ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 250 ◽  
Author(s):  
Francesco Baldassarre ◽  
Angela Altomare ◽  
Nicola Corriero ◽  
Ernesto Mesto ◽  
Maria Lacalamita ◽  
...  
Keyword(s):  
Fourier Transform ◽  
High Temperature ◽  
Inductively Coupled Plasma ◽  
Room Temperature ◽  
Annealing Temperature ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Inductively Coupled

Europium-doped hydroxyapatite Ca10(PO4)6(OH)2 (3% mol) powders were synthesized by an optimized chemical precipitation method at 25 °C, followed by drying at 120 °C and calcination at 450 °C and 900 °C. The obtained nanosized crystallite samples were investigated by means of a combination of inductively coupled plasma (ICP) spectroscopy, powder X-ray diffraction (PXRD), Fourier Transform Infrared (FTIR), Raman and photoluminescence (PL) spectroscopies. The Rietveld refinement in the hexagonal P63/m space group showed europium ordered at the Ca2 site at high temperature (900 °C), and at the Ca1 site for lower temperatures (120 °C and 450 °C). FTIR and Raman spectra showed slight band shifts and minor modifications of the (PO4) bands with increasing annealing temperature. PL spectra and decay curves revealed significant luminescence emission for the phase obtained at 900 °C and highlighted the migration of Eu from the Ca1 to Ca2 site as a result of increasing calcinating temperature.

Effect of Ni0.5Zn0.5Fe2O4 Nanoparticles Addition on Tl-1212 High Temperature Superconductor

2020 ◽  
Vol 307 ◽  
pp. 98-103
Author(s):  
Wei Kong ◽  
Christopher Jacob ◽  
Ing Kong ◽  
Cin Kong ◽  
Eng Hwa Yap ◽  
...  
Keyword(s):  
Critical Current ◽  
High Temperature Superconductor ◽  
Diffraction Method ◽  
Solid State Reaction Method ◽  
Transport Critical Current Density ◽  
X Ray Diffraction ◽  
X Ray ◽  
Oxide Powders ◽  
A Value ◽  
Average Size

The effects of Ni0.5Zn0.5Fe2O4 nanoparticle addition on the superconducting and transport properties of (Tl0.85Cr0.15)Sr2CaCu2O7 (Tl-1212) superconductor were investigated in this paper. The Tl-1212 samples were produced by mixing high purity oxide powders through a solid-state reaction method. Nano Ni0.5Zn0.5Fe2O4 particles with compositions of 0.001 wt.%, 0.003 wt.%, 0.005 wt.%, 0.01 wt.% and 0.02wt.% with average size of 60 nm were added into the Tl-1212 powders. The transition temperatures (Tc-zero and Tc-onset) were measured using a four-point probe method. The highest Tc-zero recorded was 97 K which was exhibited by the pure Tl-1212 sample. The transport critical current, Ic, of the Tl-1212 samples were found through the 1 µV/cm criterion with temperature ranging from 30 K to 77 K. The sample with a composition of 0.003 wt.% displayed the highest value of Jc at 77 K with a value ranging up to 1780 mA/cm2. The Tl-1212 samples were characterised using scanning electron microscopy (SEM), powder X-ray diffraction method (XRD), energy dispersive X-Ray analysis (EDX), electrical resistance measurements and transport critical current density measurements. The Jc of the Tl-1212 superconductor has been improved through the addition of Ni0.5Zn0.5Fe2O4 nanoparticles but adding an excessive amount has caused its Jc to degrade.

Preparation of Amorphous Calcium Phosphate/Triclcium Silicate Composite Powders

2009 ◽  
Vol 79-82 ◽  
pp. 1643-1646 ◽  
Author(s):  
Qing Lin ◽  
Yan Bao Li ◽  
Xiang Hui Lan ◽  
Chun Hua Lu ◽  
Zhong Zi Xu
Keyword(s):  
Calcium Phosphate ◽  
Shell Structure ◽  
Amorphous Calcium Phosphate ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
Core Shell ◽  
X Ray Diffraction ◽  
Composite Powders ◽  
X Ray ◽  
Core Shell Structure

The amorphous calcium phosphate (ACP)/tricalcium silicate (Ca3SiO5, C3S) composite powders were synthesized in this paper. The exothermal behavior of C3S determined by isothermal conduction calorimetry indicated that the ACP could be synthesis by chemical precipitation method during the induction period (stage II) of C3S. The composite powders were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDS). The results indicated that nanosized ACP particles deposited on the surface of C3S particles to form core-shell structure at pH=10.5, and the nCa/nP of ACP could be controlled between 1.0 and 1.5. The core-shell structure is stable after sintered at 500 oC for 3 h to remove the β-cyclodextrin (β-CD). As compared with the irregular C3S particles (1~5 μm), the composite powders particles are spherical with a diameter of 40~150 μm. Therefore, to obtain the smaller size of composite powders, it is expected to avoid the aggregate of C3S particles in the aqueous solution by addition of dispersant. As compared with C3S, the composite powders may contribute better injectability, strength and biocompatibility.

Synthesis and Characterization of Zinc Doped Hydroxyapatite for Bone Substitute Applications

2014 ◽  
Vol 660 ◽  
pp. 942-946
Author(s):  
Mohamad Firdaus Abdul Wahid ◽  
C.M. Mardziah ◽  
Koay Mei Hyie ◽  
N.R. Nik Roselina
Keyword(s):  
Crystal Size ◽  
Diffraction Method ◽  
Lattice Parameters ◽  
Phase Changes ◽  
Precipitation Method ◽  
Zinc Ions ◽  
Crystal Shape ◽  
X Ray Diffraction ◽  
X Ray

Hydroxyapatite was prepared by using precipitation method. The substitution of zinc ions in hydroxyapatite structure was studied by several characterization techniques. Several concentration of zinc ions were substituted into hydroxyapatite. Characterization technique such as X-ray diffraction method was used to study the phase changes and the lattice parameters with the addition of zinc. Field emission scanning electron microscopy was used to examine the influence of zinc on the crystal size and the morphology of the as-synthesized powders. Based on X-ray diffraction result, the addition of zinc affects the lattice parameters and phase. The result showed that zinc ions were substituted in the structure. As zinc substitution increased, the lattice parameters a and c decreased. The crystal shape of hydroxyapatite without zinc ions was regular shapes while hydroxyapatite with zinc ions was irregular and also tends to agglomerates with single particle was calculated about 28 - 34 nm .

scholarly journals The relationship between microstructure and mechanical properties of directly bonded copper-alumina ceramics joints

2014 ◽  
Vol 62 (1) ◽  
pp. 23-32 ◽  
Author(s):  
K. Pietrzak ◽  
W. Olesinska ◽  
D. Kalinski ◽  
A. Strojny-Nedza
Keyword(s):  
Mechanical Strength ◽  
Transition Layer ◽  
Diffraction Method ◽  
Alumina Ceramics ◽  
X Ray Diffraction ◽  
X Ray ◽  
Three Point Bending ◽  
Microscopy Method ◽  
Materials Used ◽  
The Individual

Abstract The effect of phase transformations induced in the surface layer of alumina ceramics during its direct joining with copper activated with oxygen or titanium on the mechanical strength of the ceramic/copper joints was examined. The materials used in the experiments were an alumina single crystal, alumina ceramics (97.5 wt% Al2O3), the cermet mixtures: Cu-Cu2O with 10-50 wt% of Cu2O, copper with 5 wt% of Ti, and copper with 5 wt% of Ti and 10 wt% of Ag. The microstructure of the transition layer was examined by the X-ray diffraction method (XRD), scanning electron microscopy method (SEM) and energy dispersive x-ray spectroscopy (EDX). The mechanical strength of the joints was measured using the three-point bending method. The amount of oxygen optimal for the joining process was determined. It has been demonstrated that the cohesion of the joints depends not only on the formation of the individual phases but also, or even primarily, on the microstructure of the transition layer formed between them.

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