Preparation and Characterization of NiO Nanoparticles

2015 ◽  
Vol 31 ◽  
pp. 93-102 ◽  
Author(s):  
Farrakh Shahzad ◽  
Karl Ettinger ◽  
Ilse Letofsky-Papst ◽  
Julia Weber ◽  
Peter Knoll

NiO nanoparticles are successfully prepared by sol-gel technique. A systematic change in preparation parameters like calcination temperature, calcination time and pH value has been done in order to study the influence on crystallite size. The prepared samples are characterized by X-ray diffractometer, Transmission electron microscopy, Energy dispersive x-rays analysis and Raman spectroscopy. It is shown that crystallite size mainly depends on the calcination temperature rather than pH value or calcination time.

2020 ◽  
Vol 3 (3) ◽  
Author(s):  
Jothi M ◽  
Sowmiya K

Nickel Oxide (NiO) is an important transition metal oxide with cubic lattice structure. NiO is thermally stable that is suitable for tremendous applications in the field of optic, ceramic,glass, electro-chromic coatings, plastics, textiles, nanowires, nanofibers, electronics,energy technology, bio-medicine, magnetism and so on. In this present study, NiO nanoparticles were successfully synthesized by sol-gel technique. Nano-sols were prepared by dissolving Nickel-Chloride [NiCl2.6H2O] in NaOH solvent and were converted into nano structured gel on precipitation. A systematic change in preparation parameters like calcination temperature, time, pH value has been noticed in order to predict the influence on crystallite size. Then the prepared samples were characterized by the X-ray Diffraction Spectroscopic (XRD), UV-VIS Spectroscopy, Fourier Transform Infra-Red Spectroscopy (FTIR), Energy Dispersive X-ray Spectroscopy (EDX), Scanning Electron Microscopy (SEM) and Particle Size Analyzer (PSA). From XRD, the average crystalline-size has been calculated by Debye-Scherrer Equation and it was found to be 12.17 nm and the band gap energy of Nickel oxide (NiO) from UV studies reveals around 3.85 eV. Further, EDX and FTIR studies, confirm the presences of NiO nanoparticles. The SEM study exhibits the spherical like morphology of Nickel oxide (NiO). Further from PSA, the mean value of NiO nanoparticles has been determined.


2010 ◽  
Vol 148-149 ◽  
pp. 1575-1579
Author(s):  
Qing Zhang ◽  
Rui Yuan Niu ◽  
Min Wang ◽  
Bin Cui ◽  
Zhu Guo Chang

Li-Ti-O (abbreviated as LTO) nano-composites were synthesized via sol-gel process, and then doped BaTiO3 based X7R type ceramics. The LTO nano-composites and their ceramics were characterized by means of thermaogravimetric, Fourier-transform infrared, X-ray diffraction methods, transmission electron microscopy. We also characterized the dielectric properties of the LTO doped BaTiO3 based ceramics of X7R type. The results indicated that LTO nano-composites were nanometer scale powders. The pH value and calcining temperature had an influence on particle size of LTO sintering aids. At pH about 3 and with calcining at 600 °C, the nano-composites attained minimum particle size (about 10 nm). By adding 0.10 wt% of the LTO nano-composites, the temperature permittivity achieved about 4200 when sintered at 1240 °C for 4 h, and the dielectric properties met X7R standard.


2020 ◽  
Vol 1007 ◽  
pp. 47-51
Author(s):  
Huynh Tuyet Anh Le ◽  
Tuan Anh Nguyen ◽  
Ky Phuong Ha Huynh

Antibacterial materials based on nanotechnology have been attracted considerable attention by the scientific community. In this study, the sol-gel method was applied to prepare of antibacterial materials from tetra-n-butyl orthotitanate, zinc nitrate and ethylenediamine tetraacetic acid (EDTA) as a complexing agent. The effects of the synthesis conditions on the properties of the Ag/ZnTiO3 samples such as the calcination temperature, the calcination time, pH value and ethylene glycol volume, were investigated. The obtained materials were characterized by powder X-ray diffraction (XRD) and their antibacterial activity against Staphylococcus aureus (S. Aureus) was evaluated. The results showed that the optimum conditions for Ag/ZnTiO3 synthesis were: calcination temperature of 650°C, calcination time of 2 h, pH value of 4.5 and ethylene glycol volume of 4.5 mL.


2011 ◽  
Vol 2011 ◽  
pp. 1-6 ◽  
Author(s):  
L. A. García-Cerda ◽  
K. M. Bernal-Ramos ◽  
Sagrario M. Montemayor ◽  
M. A. Quevedo-López ◽  
R. Betancourt-Galindo ◽  
...  

The preparation and characterization of hcp and fcc Ni and Ni/NiO nanoparticles is reported. Ni and Ni/NiO nanoparticles were obtained starting from a precursor material prepared using a citric assisted Pechini-type method and, then, followed by a calcination of the precursor in air at either 400 or 600°C for different times. The precursor was analyzed using thermogravimetric and differential thermal methods (TGA-DTA), and the resulting nanoparticles were characterized by X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), and vibrational sample magnetometry. Nanoparticles showed a phase transformation for Ni from hcp to fcc and/or to fcc NiO structure as the calcination time increased. The influence of the phase transition and the formation of NiO on the magnetic properties of the samples are discussed.


1995 ◽  
Vol 18 (1) ◽  
pp. 53-60 ◽  
Author(s):  
S. D. Han ◽  
S. Y. Huang ◽  
G. Campet ◽  
M. A. Kennard ◽  
Y. M. Son

The evolution of the specific surface area and crystallite size of SnO2powders, prepared from a sol-gel process, was studied as a function of the calcination temperature of the stannic hydroxyde colloid, and for two different pH values (7.5 and 12.5) of the colloïdal state. The samples were characterized by TGA, IR spectroscopy, BET, and XRD techniques. The crystallite size and specific surface area were strongly affected not only by the calcination temperature, but unexpectedly, by the initial pH value of the colloïdal state. A framework model, relating the pH dependence to the resulting properties, is presented.


2005 ◽  
Vol 38 (1) ◽  
pp. 211-216 ◽  
Author(s):  
Pang-Hung Liu ◽  
Kuei-Jung Chao ◽  
Xing-Jian Guo ◽  
Kuo-Ying Huang ◽  
Yen-Ru Lee ◽  
...  

A continuous silica film with well aligned mesochannels parallel to the Si(001) surface was found to be formed through sol–gel dip-coating of a silica precursor with nonionic ethylene oxide surfactant. Two two-dimensional mesoporous structures in centered and non-centered rectangular symmetries and with the short axes of elongated ellipsoidal pores normal to the surface were observed by X-ray and electron diffraction. Detailed transmission electron microscopy investigations were employed to view the direction dependence of the channel or pore packing in the continuous film.


2015 ◽  
Vol 29 (01) ◽  
pp. 1450254 ◽  
Author(s):  
M. Shayani Rad ◽  
A. Kompany ◽  
A. Khorsand Zak ◽  
M. E. Abrishami

Pure and silver added zinc oxide nanoparticles ( ZnO -NPs and ZnO : Ag -NPs) were synthesized through a modified sol–gel method. The prepared samples were characterized using X-ray diffraction (XRD), transmission electron microscopy (TEM) and photoluminescence (PL) spectroscopy. In the XRD patterns, silver diffracted peaks were also observed for the samples synthesized at different calcination temperatures of 500°C, 700°C, 900°C except 1100°C, in addition to ZnO . TEM images indicated that the average size of ZnO : Ag -NPs increases with the amount of Ag concentration. The PL spectra of the samples revealed that the increase of Ag concentration results in the increase of the visible emission intensity, whereas by increasing the calcination temperature the intensity of visible emission of the samples decreases.


2013 ◽  
Vol 284-287 ◽  
pp. 230-234
Author(s):  
Yu Jen Chou ◽  
Chi Jen Shih ◽  
Shao Ju Shih

Recent years mesoporous bioactive glasses (MBGs) have become important biomaterials because of their high surface area and the superior bioactivity. Various studies have reported that when MBGs implanted in a human body, hydroxyl apatite layers, constituting the main inorganic components of human bones, will form on the MBG surfaces to increase the bioactivity. Therefore, MBGs have been widely applied in the fields of tissue regeneration and drug delivery. The sol-gel process has replaced the conventional glasses process for MBG synthesis because of the advantages of low contamination, chemical flexibility and lower calcination temperature. In the sol-gel process, several types of surfactants were mixed with MBG precursor solutions to generate micelle structures. Afterwards, these micelles decompose to form porous structures after calcination. Although calcination is significant for contamination, crystalline and surface area in MBG, to the best of the authors’ knowledge, only few systematic studies related to calcination were reported. This study correlated the calcination parameters and the microstructure of MBGs. Microstructure evaluation was characterized by transmission electron microscopy and nitrogen adsorption/desorption. The experimental results show that the surface area and the pore size of MBGs decreased with the increasing of the calcination temperature, and decreased dramatically at 800°C due to the formation of crystalline phases.


2021 ◽  
Vol 317 ◽  
pp. 447-453
Author(s):  
Noor Hidayah Aniza Zakaria ◽  
Nafisah Osman

NiO nanoparticle was synthesized by a sol-gel method with three different pH values namely pH=1, 7 and 11, and then calcined at temperature of 450 ᵒC. The influence of different pH values on the physical properties of NiO nanoparticles were investigated by a particle size analyzer (PSA), field emission scanning electron microscope (FESEM) and X-ray diffractometer (XRD). Structural analysis confirmed that a cubic structure of NiO nanoparticle was obtained without any secondary phase for NiO powders prepared with pH=1, while the peak of secondary phase (Ni) appeared for NiO powders prepared with pH= 7 and 11. Morphological observation showed that the NiO nanoparticles prepared with pH=7 and 11 tend to form more agglomerates compared to one prepared with pH=1. The average diameter of NiO nanoparticles with pH 1, 7 and 11 were approximately in the range of 19-26 nm, 21-28 nm, and 24-30 nm, respectively. NiO powder that was synthesized with pH=1 was further used to prepare composite anode of NiO Nps-BaCe0.54Zr0.36Y0.1O2.95 (BCZY) powder. Unfortunately a composite of NiO Nps-BaCeO3-BaZrO3 was obtained instead of BCZY and governed by agglomerates with size in the range of 70-300 nm.


2016 ◽  
Vol 3 (1) ◽  
pp. 12-14
Author(s):  
Kalpanadevi K ◽  
Manimekalai R

Nickel oxide (NiO) nano-particles were produced via a simple microwave method from the Ni(OH)2 precursor, which was obtained by slow drop-wise addition of 0.1M sodium hydroxide to 0.1M nickel nitrate. The mixture was vigorously stirred until the pH reached 7.2. The mixture was then irradiated with microwave to deposit Ni(OH)2 at a better precipitation rate. Drying the precipitate at 320°C resulted in formation of NiO nanoparticles. High Resolution Transmission Electron Microscope (HRTEM), Scanning Electron Microscope (SEM) and X-ray diffraction (XRD), employed for the structural characterization of the as-prepared NiO nanoparticles, revealed their good crystallinity and high-purity. Microwave irradiation increased homogeneity and decreased the mean particle size of the produced NiO particles.


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