Characterisation of undoped Zns and fecl3 doped Zns nanoparticles are synthesized by chemical precipitation method

2020 ◽  
Vol 3 (2) ◽  
Author(s):  
Aarthe K G ◽  
Kiruthika P
Keyword(s):  
Xrd Analysis ◽  
Chemical Precipitation ◽  
Zinc Sulphide ◽  
Chemical Precipitation Method ◽  
Precipitation Method ◽  
Flat Panel Displays ◽  
X Ray Diffraction ◽  
Nano Structure ◽  
X Ray ◽  
Vibrational Bands

Nanoparticles of Ferric chloride (FeCl3) doped Zinc Sulphide (ZnS) and Undoped Zinc Sulphide (ZnS) had been synthesized successfully by simple chemical precipitation method. Particlesizes have been calculated from X-ray diffraction (XRD) analysis which confirms the nano structure of the samples. The Molecular structure of the compound was determined by theFourier transform infrared spectroscopy (FTIR) analysis and the different vibrational bands confirmed the functional groups present in the sample. The bandwidth of the absorbance isexamined by using (UV)-Visible Spectroscopy. The Morphological structures have been confirmed by using Scanning Electron Microscope (SEM). Energy Dispersive analysis of X-ray (EDAX) shows the composition of elements present in the nanoparticles. The applications of ZnS were used in the field such as Field Emitting Diodes (FET), sensors (gas sensors, biosensors), Flat panel displays, Electroluminescence.

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...

Synthesis and characterization of zinc doped copper oxide nanocrystals by chemical precipitation method

2020 ◽  
Vol 3 (2) ◽  
Author(s):  
Aarthe K G ◽  
Sowmiya V
Keyword(s):  
Copper Oxide ◽  
Copper Acetate ◽  
Morphological Structure ◽  
Visible Spectrum ◽  
Chemical Precipitation ◽  
Copper Oxide Nanoparticles ◽  
Chemical Precipitation Method ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray

Zinc doped copper oxide nanoparticles were synthesized by chemical precipitation method. Copper acetate is act as a precursor and sodium hydroxide will act as a reducing agent. The prepared nanoparticles were characterized by X-ray diffraction (XRD) which reveals the simple monoclinic structure. The Fourier Transform Infrared Spectroscopy confirms the functional groups present in the nano powders. The morphological Structure of the prepared crystals are analyzed by Scanning Electron Microscopy (SEM) were showed that the products consists of flaky in nature. The Bandwidth of the synthesized sample was calculated by UV- visible spectrum. The presence of compounds in nano powders were confirmed by Energy Dispersive X-ray diffraction (EDAX). Copper oxide has applications as a P-type semiconductor, because it has a narrow band gap of energy of 1.2 e V. Zinc doped copper oxide has applications in the wide variety of fields such as medicine, industries, sunscreens, agriculture etc.

X-Ray Diffraction Analysis of YSAG:Yb Ceramic Powders with Different Stoichiometry

2020 ◽  
Vol 310 ◽  
pp. 1-5
Author(s):  
Marina S. Nikova ◽  
Dmitry S. Vakalov ◽  
Vitaly A. Tarala ◽  
Irina S. Chikulina ◽  
Fedor F. Malyavin ◽  
...  
Keyword(s):  
Diffraction Analysis ◽  
Chemical Precipitation ◽  
Chemical Precipitation Method ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Ceramic Powders ◽  
Oxide Composition ◽  
X Ray ◽  
Garnet Phase

Synthesis of YSAG:Yb ceramic powders with different stoichiometry by chemical precipitation method was carried out. It has been established that scandium can replace both dodecahedral and octahedral positions of garnet. It is shown that scandium is embedded in those positions that become available to it when the YAG:Yb composition deviates from stoichiometric. Thus, scandium can compensate for the lack of one of the components of the oxide composition Y2O3, Yb2O3, and Al2O3 during the formation of the garnet phase.

Cadmium Zinc Sulphide Nanoparticles as Sensing Material for Microcontroller Based Ammonia Sensor: Pilot Study

2014 ◽  
Vol 781 ◽  
pp. 119-126
Author(s):  
M. Azimul Haque ◽  
S. Mahalakshmi ◽  
Ritesh Nanwal
Keyword(s):  
Chemical Precipitation ◽  
Zinc Sulphide ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Multiple Parameters ◽  
Ammonia Sensing ◽  
Sensing Material ◽  
Labview Program ◽  
Cadmium Zinc

A microcontroller based sensor was designed for ammonia sensing. Cadmium zinc sulphide (CdZnS) nanoparticles were used as the sensing material. CdZnS nanoparticles were synthesized by chemical precipitation method. Synthesized CdZnS nanoparticles were characterized using X-ray diffraction (XRD), Field emission scanning electron microscope (FE-SEM) and Energy dispersive X-ray spectroscopy (EDS). CdZnS nanoparticles were deposited as thick films on glass substrate to act as gas sensor and its response to ammonia vapours was recorded using LabVIEW program interfaced with the microcontroller. The preliminary studies revealed that CdZnS nanoparticles can be used for ammonia sensing and the microcontroller based sensor design on proper calibration and integration can lead to the fabrication of a handheld sensor for sensing multiple parameters.

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.

scholarly journals Effect of Annealing on the ZnS Nanocrystals Prepared by Chemical Precipitation Method

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Nadana Shanmugam ◽  
Shanmugam Cholan ◽  
Natesan Kannadasan ◽  
Kannadasan Sathishkumar ◽  
G. Viruthagiri
Keyword(s):  
Chemical Precipitation ◽  
Chemical Precipitation Method ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Visible Absorption ◽  
Atomic Force ◽  
Transmission Electron ◽  
Different Temperatures ◽  
Uv Visible ◽  
Dta Curves

Nanocrystals of ZnS have been synthesized through simple chemical precipitation method using thiourea as sulphur source. The synthesized products were annealed at different temperatures in the range of 200–800∘C. The as-synthesized and annealed samples were characterized by X-ray diffraction (XRD), UV-Visible absorption (UV-Vis), and room temperature photoluminescence (PL) measurements. The morphological features of ZnS annealed at 200 and 500∘C were studied by atomic force microscope (AFM) and transmission electron microscope (TEM) techniques. The phase transformation of ZnS and formation of ZnO were confirmed by thermogravimetric (TG) and differential thermal analysis (DTA) curves.

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.

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.

Size Controllable Synthesis and Characterization of CuO Nanostructure

2018 ◽  
Vol 915 ◽  
pp. 98-103 ◽  
Author(s):  
Duygu Candemir ◽  
Filiz Boran
Keyword(s):  
Freeze Drying ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Peg 4000 ◽  
Structure Morphology ◽  
Cuo Nanostructure

In this study, copper oxide (CuO) nanostructures were successfully prepared by adding EG (ethylene glycol) and PEG (4000, 8000) (polyethylene glycol) via an in-situ chemical precipitation method. EG and PEG (4000, 8000) were effective for changing the particular size of CuO and we examined the effects of drying type such as freeze drying, muffle and horizontal furnace on the size of CuO nanostructure. The structure, morphology and elemental analysis of CuO nanostructure were analyzed by field-emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDS). Also, the CuO nanostructures showed excellent electrical conductivity by the changing of PEG’s molecular weight and drying processes.

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