MICROWAVE-ASSISTED SYNTHESIS AND CHARACTERIZATION OF CaS NANOPARTICLES

2012 ◽  
Vol 11 (05) ◽  
pp. 1250027 ◽  
Author(s):  
ARUP ROY ◽  
JAYANTA BHATTACHARYA
Keyword(s):  
Microwave Irradiation ◽  
Average Particle Size ◽  
Microwave Assisted Synthesis ◽  
Average Particle ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy ◽  
One Step ◽  
Diffraction Patterns ◽  
Powder Analysis

CaS nanoparticles have been synthesized by microwave irradiation, using Ca(Ac)2 as Ca -precursor, and thioacetamide as S -source. The as-prepared sample has a uniform morphology and high purity. After heat treatment similar results were observed. Synthesized nanoparticles were characterized by X-ray powder analysis (XRD), field emission scanning microscopy (FESEM), high resolution transmission electron microscopy (TEM), and UV-Vis absorption spectroscopy. X-ray diffraction patterns suggest the formation of single cubical face of CaS having average particle size of 22 nm. HRTEM micrographs reveal well dispersed cubical morphology with a size distribution of 18–30 nm. Ultraviolet-visible (UV-Vis) spectroscopy shows absorption at 268 nm. In nutshell, microwave irradiation is proved to be a convenient, efficient and environmental-friendly one-step route to synthesize nanoparticles.

scholarly journals Rapid Synthesis of Gold Nanoparticles with Ginger Waste using Microwave Irradiation

2019 ◽  
Vol 32 (2) ◽  
pp. 471-476
Author(s):  
G. Bhagavanth Reddy ◽  
B. Rajkumar ◽  
K. Girija Mangatayaru ◽  
T.V.D. Prasad Rao
Keyword(s):  
Gold Nanoparticles ◽  
Zeta Potential ◽  
Microwave Irradiation ◽  
Pathogenic Bacteria ◽  
Average Particle Size ◽  
Average Particle ◽  
X Ray ◽  
Transmission Electron ◽  
Uv Visible ◽  
The Stability

In the present investigation, synthesis of gold nanoparticles (AuNPs) was carried out with microwave irradiation of HAuCl4 and the extract of ginger waste. Synthesized AuNPs were characterized by various techniques including UV-visible spectroscopy (UV-vis), Fourier transform infrared spectroscopy (FTIR), X-ray powder diffraction (XRD), dynamic light scattering (DLS) and transmission electron microscopy (TEM). The TEM images revealed that the nanoparticles were spherical in shape and the average particle size of the AuNPs was found to be approximately 6 ± 2 nm. The stability of gold nanoparticles was analyzed by zeta potential measurements. A negative zeta potential value of -18.4 mV indicates the stability of the AuNPs. Further, gold nanoparticles exhibited the excellent catalytic activity in reducing 4-nitrophenol to 4-aminophenol in the presence of NaBH4 (reducing agent), and it was found to depend on the amount of AuNPs and temperature. Gold nanoparticles did not show any significant antibacterial activity against the pathogenic bacteria studied.

The Aggregation Study and Characterization of Silver Nanoparticles

2017 ◽  
Vol 263 ◽  
pp. 165-169
Author(s):  
Silvia Chowdhury ◽  
Faridah Yusof ◽  
Nadzril Sulaiman ◽  
Mohammad Omer Faruck
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Particle Size ◽  
Silver Nanoparticles ◽  
Absorption Spectrum ◽  
Average Particle Size ◽  
Average Particle ◽  
Transmission Electron ◽  
Vis Spectroscopy

In this article, we have studied the process of silver nanoparticles (AgNPs) aggregation and to stop aggregation 0.3% Polyvinylpyrrolidone (PVP) was used. Aggregation study carried out via UV-vis spectroscopy and it is reported that the absorption spectrum of spherical silver nanoparticles were found a maximum peak at 420 nm wavelength. Furthermore, Transmission Electron Microscopy (TEM) were used to characterized the size and shape of AgNPs, where the average particle size is around 10 to 25 nm in diameter and the AgNPs shape is spherical. Next, Dynamic Light Scattering (DLS) were used, owing to observed size distribution and self-correlation of AgNPs.

Biosynthesis and Characterization of Copper Nanoparticles Using a Bioflocculant Extracted from Alcaligenis faecalis HCB2

2019 ◽  
Vol 11 (11) ◽  
pp. 1064-1070 ◽  
Author(s):  
Nkosinathi G. Dlamini ◽  
Albertus K. Basson ◽  
V. S. R. Rajasekhar Pullabhotla
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Copper Nanoparticles ◽  
Average Particle Size ◽  
Thermo Gravimetric Analysis ◽  
Average Particle ◽  
Gravimetric Analysis ◽  
X Ray ◽  
Transmission Electron ◽  
Ft Ir

Bioflocculant from Alcaligenis faecalis HCB2 was used in the eco-friendly synthesis of the copper nanoparticles. Nanoparticles were characterized using a scanning electron microscope (SEM), transmission electron microscopy (TEM), UV-visible spectroscopy, thermo gravimetric analysis (TGA) and Fourier Transform Infrared Spectroscopy (FT-IR). The transmission electron microscopy images showed close to spherical shapes with an average particle size of ∼53 nm. Energy-dispersive X-ray spectroscopy analysis confirmed the presence of the Cu nanopartilces and also the other elements such as O, C, P, Ca, Cl, Na, K, Mg, and S originated from the bioflocculant. FT-IR results showed the presence of the –OH and –NH2 groups, aliphatic bonds, amide and Cu–O bonds. Powder X-ray diffraction peaks confirmed the presence of (111) and (220) planes of fcc structure at 2 of 33° and 47° respectively with no other impurity peaks.

DIELECTRIC PROPERTIES OF ULTRAFINE Zn-DOPED CaCu3Ti4O12 CERAMIC

2012 ◽  
Vol 02 (01) ◽  
pp. 1250007 ◽  
Author(s):  
LAXMAN SINGH ◽  
U. S. RAI ◽  
K. D. MANDAL ◽  
MADHU YASHPAL
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Room Temperature ◽  
Single Phase ◽  
Average Particle Size ◽  
Average Particle ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Sintered Powder

Ultrafine powder of CaCu2.80Zn0.20Ti4O12 ceramic was prepared using a novel semi-wet method. DTA/TG analysis of dry powder gives pre-information about formation of final product around 800°C. The formation of single phase was confirmed by X-ray diffraction analysis. The average particle size of sintered powder of the ceramic obtained from XRD and Transmission electron microscopy was found 59 nm and 102 nm, respectively. Energy Dispersive X-ray studies confirm the stoichiometry of the synthesized ceramic. Dielectric constant of the ceramic was found to be 2617 at room temperature at 1 kHz.

Studies on conducting nanocomposite with gallium nitride–doped ferrite, part-II

2017 ◽  
Vol 231 (1) ◽  
pp. 53-63
Author(s):  
Rajani Indrakanti ◽  
V Brahmaji Rao ◽  
C Udaya Kiran
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Gallium Nitride ◽  
Crystallite Size ◽  
Average Particle Size ◽  
Average Particle ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

This article (a sequel to part-I that appeared earlier in the same journal) presents synthesis and characterisation details of conducting PPY-nanocomposite obtained from gallium nitride–doped ferrite and polypyrrole. The GaN-doped ferrite is synthesised by sol–gel method. GaNFe2O3f-PPY composites are prepared by impregnation technique. Using the SciFinder software we could not trace any report in the literature for this synthesised Ga(2x + 2)NFe2(49 − x)O3-PPY nanocomposites. The doped nanoferrite is combined with polypyrrole, an intrinsic conducting polymer, in three proportions by percentage (70%:30%), (90%:10%) and (97%:3%), to obtain two series each of three compositions for the conducting PPY-nanocomposite. The synthesised polymer composites are characterised by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, selected area electron diffraction, energy dispersive X-ray analysis and Fourier transform infrared spectroscopy. From our studies, it has been observed that the crystallite size of nanocomposites is decreased when compared to crystallite size of GaNFe2O3. The average particle size from histogram is in good agreement with Debye–Scherrer formula calculations. The scanning electron microscopy and transmission electron microscopy micrograms reveal that the particles are varying with the values of X and the percentage of PPY. The shapes observed are Globules,Tetrahedron,Nanorods of short and long lengths. The GaNFe2O3-PPY composites’ spectra revealed the shift in the band in comparison with the PPY spectra. Also, the wavelength is decreased, and vibrational frequency is increased.

SYNTHESIS OF YTTRIA-STABILIZED CUBIC ZIRCONIA NANOCRYSTALS BY ULTRASONIC–MICROWAVE ROUTE

NANO ◽  
2010 ◽  
Vol 05 (05) ◽  
pp. 271-277 ◽  
Author(s):  
JIAN-DONG WANG ◽  
CHONG-XIAO LUO ◽  
JIN-KU LIU ◽  
YI LU ◽  
GUANG-MING LI
Keyword(s):  
Average Particle Size ◽  
Degree Of Crystallinity ◽  
Average Particle ◽  
Stabilized Zirconia ◽  
Uniform Size ◽  
X Ray ◽  
Microwave Assisted ◽  
Transmission Electron ◽  
High Degree ◽  
Microwave Assisted Method

The yttria-stabilized zirconia (YSZ) nanocrystals with uniform size, high purity, and high degree of crystallinity, were prepared by ultrasonic–microwave-assisted method. The structure, optical properties and morphologies of YSZ nanocrystals were characterized by X-ray powder diffraction (XRD), Raman spectroscopy, UV–vis absorption, scanning electron microscope (SEM) and transmission electron microscopy (TEM). The SEM and TEM images of the YSZ nanocrystals indicate that the product is a mono-dispersion structure with an average particle size of about 25 nm.

The Impregnating Reduction Method for Synthesis of Pt–Ru Nanoparticles and Its Catalytic Performance for Methanol Electro-oxidation

2015 ◽  
Vol 12 (4) ◽  
Author(s):  
Long-long Wang ◽  
Hong-min Mao ◽  
Xiao-jin Zhou ◽  
Qun-jie Xu ◽  
Qiao-xia Li
Keyword(s):  
Reduction Method ◽  
Average Particle Size ◽  
Catalytic Performance ◽  
Average Particle ◽  
X Ray ◽  
Onset Potential ◽  
Ru Nanoparticles ◽  
Oxidation Of Methanol ◽  
Transmission Electron ◽  
Electro Oxidation

Well-dispersed and low Pt content Pt–Ru/C nanoparticles were prepared by a developed impregnating reduction method with sodium citrate as stabilizer. The as-prepared Pt–Ru/C catalysts were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), and energy dispersive X-ray (EDX) analysis. TEM showed that the Pt–Ru particles were quite uniformly distributed on the surface of the carbon with an average particle size of 3.5–4.5 nm. The effect of pH values on methanol electro-oxidation reaction was examined by cyclic voltammetry (CV) and chronoamperometry (CA). Pre-adsorbed CO monolayer stripping was used to evaluate the antipoisoning ability. The results showed that Pt–Ru/C (pH = 8) catalyst had the highest catalytic activity and stability toward the oxidation of methanol. Finally, comparing Pt–Ru/C (Pt–Ru 20 wt.%, Pt/Ru = 1:1) catalysts with Pt/C (Pt 20 wt.%), the onset potential was 200 mV lower and electrochemical active area was much bigger.

Investigation on Carbonizing Behaviors of Nanometer-sized Cr2O3 Particles Dispersed on Alumina Particles by Metalorganic Chemical Vapor Deposition in Fluidized Bed

2005 ◽  
Vol 20 (8) ◽  
pp. 2154-2160 ◽  
Author(s):  
Hao-Tung Lin ◽  
Jow-Lay Huang ◽  
Wen-Tse Lo ◽  
Wen-Cheng J. Wei
Keyword(s):  
Chemical Vapor Deposition ◽  
Vapor Deposition ◽  
Graphite Furnace ◽  
Average Particle Size ◽  
Chemical Vapor ◽  
Average Particle ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Alumina Particles

Nanoscaled Cr2O3 powder with an average particle size of 20–40 nm, coated on alumina particles, has been produced by means of chemical vapor deposition (CVD) in a fluidized chamber, using the pyrolysis of Cr(CO)6 precursor. Amorphous and crystalline Cr2O3 particles were obtained when the temperatures of the pyrolysis were 300 and 400 °C, respectively. To prepare nanoscaled Cr3C2 powder from the nanometer-sized Cr2O3, carbonizing behavior of the Cr2O3 particles was investigated. It was found that, when amorphous Cr2O3 powders were carbonized in graphite furnace at 1150 °C for 2 h in vacuum (10−3 Torr), the powder was transformed into Cr3C2, while the crystalline Cr2O3 was transformed into a mixture of Cr7C3 and Cr3C2. The examinations by x-ray diffraction, transmission electron microscopy, and energy dispersive spectroscopy confirmed the transformation of the nano-sized Cr3C2 powders. The results of thermogravimetry and differential thermal analysis indicated that the transformation temperature was ∼1089 °C for amorphous Cr2O3 and ∼1128 °C for crystalline Cr2O3.

The concentration quenching of photoluminescence in Eu3+-doped La2O3

2013 ◽  
Vol 37 (1) ◽  
pp. 47-54 ◽  
Author(s):  
V. Đorđević ◽  
Ž. Antić ◽  
M. G. Nikolić ◽  
M. D. Dramićanin
Keyword(s):  
Room Temperature ◽  
Hexagonal Phase ◽  
Average Particle Size ◽  
Average Particle ◽  
X Ray Diffraction ◽  
X Ray ◽  
Maximum Lifetime ◽  
Transmission Electron ◽  
Lifetime Value ◽  
Kinetics Of

Abstract This work explores the influence of dopant concentration on photoluminescent emission and kinetics of Eu3+-doped (0.2−10 at.%) nanocrystalline lanthanumoxide powders. The X-ray diffraction analysis confirmed that all samples crystallize in La2O3 hexagonal phase with space group P3¯ m1. Transmission electron microscopy showed particles with non-uniform shape and diverse size distribution with an average particle size of (95 ± 5) nm. The room temperature photoluminescence spectra of all samples contain characteristic Eu3+ luminescence lines with the most pronounced red 5D0 →7F2 emission at about 626 nm. The maximum intensity of red emission is observed for the sample containing 5at.% of Eu3+ ions. The emission kinetics was recorded in the temperature range from 10K to 300 K. The maximum lifetime value of 0.98 ms obtained for the sample with 0.5at.% Eu3+ at room temperature increases up to 1.3ms at 10 K.

scholarly journals Influence of Cr2O3 Nanoparticles on the Structural, Optical, Thermal and Electrical Properties of PEO/CMC Nanocomposites

2021 ◽  
Author(s):  
Laila Gaabour
Keyword(s):  
Energy Gap ◽  
Average Particle Size ◽  
Nanocomposite Films ◽  
Average Particle ◽  
Cole Plot ◽  
Optical Energy Gap ◽  
X Ray ◽  
Vis Spectroscopy ◽  
Cr2o3 Nanoparticles ◽  
A Charge

Abstract In the present paper, different concentrations of chromium oxide (Cr2O3) nanoparticles were incorporated within PEO/CMC polymer blend to produce nanocomposite films using the casting method. The X-ray diffraction was performed on PEO/CMC-Cr2O3 nanocomposites. The main X-ray peaks of Cr2O3 were observed and defined as cubic structure and orthorhombic shape with an average particle size of the Cr2O3 ~ 50-80 nm. The decrease of some IR bands after the addition of Cr2O3 nanoparticles was found attributed to the interactions between PEO/CMC and Cr2O3. Effect of Cr2O3 nanoparticles on optical properties such as absorbance and optical energy gap (Eg) were characterized using UV-Vis spectroscopy. The Eg was reduced after the addition of Cr2O3 nanoparticles. The AC conductivity (sac), dielectric constant (ε′), dielectric loss (ε′′) and the dielectric modulus (M′ and M′′) were calculated at frequency range 0.1 Hz-7 GHz. The increases of direct conductivity (σdc) imply that the free charge density or of the charge mobility that results. The estimated values of both ε′ and ε′′ were decreased with increases of frequency. The addition of Cr2O3 nanoparticles causes the formation of a charge-transfer complex. The Cole-Cole plot between (M′ and M′′) shows a semi-circular shape confirm discuses according to a non‐Debye method.

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