scholarly journals Synthesis and Characterization of the CaTiO3:Eu3+ Red Phosphor by an Optimized Microwave-Assisted Sintering Process

Materials ◽  
2020 ◽  
Vol 13 (4) ◽  
pp. 874
Author(s):  
Haifeng Wang ◽  
Jianwei Lu ◽  
Ruoxuan Wang ◽  
Yungu Dong ◽  
Linfeng Ding
Keyword(s):  
Red Light ◽  
Precipitation Method ◽  
Synthesis Process ◽  
Sintering Process ◽  
Time Saving ◽  
Red Phosphor ◽  
Microwave Assisted ◽  
Furnace Sintering ◽  
Co Precipitation

The synthesis process has a significant influence on the properties of Ca1-xTiO3:Eu3+x phosphors; thus, an optimized process will lead to a better performance of the Ca1-xTiO3:Eu3+x phosphors. In this work, the feasibility of synthesizing the Ca1-xTiO3:Eu3+x phosphor with a good luminescent performance by combining the chemical co-precipitation method and microwave-assisted sintering was studied. The precursor of Ca1-xTiO3:Eu3+x phosphors were prepared by the chemical co-precipitation method. To find an optimized process, we applied both of the traditional (furnace) sintering and the microwave-assisted sintering to synthesize the Ca1-xTiO3:Eu3+x phosphors. We found out that a sintering power of 528 W for 50 min (temperature around 950 °C) by a microwave oven resulted in similar emission intensity results compared to traditional furnace sintering at 900 °C for 2.5 h. The synthesized Ca1-xTiO3:Eu3+x phosphors has an emission peak at 617 nm (5D0→7F2), which corresponds to the red light band. This new synthesized method is an energy efficient, time saving, and environmentally friendly means for the preparation of Ca1-xTiO3:Eu3+x red phosphor with good luminescent performance.

Preparation and Characterization of Superparamagnetic Fe3O4 Nanoparticles with Controlled Sizes

2011 ◽  
Vol 335-336 ◽  
pp. 960-963
Author(s):  
Jian Bo Qu ◽  
Guang Lun Jing ◽  
Hai Long Xu ◽  
Xiao Xiao Zhang
Keyword(s):  
Particle Size ◽  
Aging Time ◽  
Particle Diameter ◽  
Precipitation Method ◽  
Hydrothermal Temperature ◽  
Microwave Assisted ◽  
Chemical Approach ◽  
Co Precipitation

A facile chemical approach of preparing magnetic Fe3O4nanoparticles with controlled sizes was developed by microwave-assisted co-precipitation method. By changing the synthetic conditions, particle diameter can be tuned from 9.6 to 19 nm. The results indicate that the hydrothermal temperature (HT) and consequent aging time play important roles in controlling of the particle size and crystallization.

scholarly journals A study on synthesis and characterization of Dy-dopedLa0.6Sr0.4Co0.2Fe0.8O3-δvia co precipitation method

2020 ◽  
Author(s):  
Negin Mohammadi ◽  
Zahra Khakpour ◽  
Amir Maghsoudipour ◽  
Aida Faeghinia
Keyword(s):  
Phase Formation ◽  
Perovskite Phase ◽  
Average Particle Size ◽  
Xrd Analysis ◽  
Precipitation Method ◽  
Synthesis Process ◽  
Average Particle ◽  
Powder Morphology ◽  
Co Precipitation

Abstract The perovskite Lanthanum Strontium Cobalt Ferrite (LSCF) is investigated as the cathode material used in intermediate temperature solid oxide fuel cells (IT-SOFCs). In the present study, La0.6-xDyxSr0.4Co0.2Fe0.8O3-δ(x= 0, 0.3, 0.6) was synthesized through co precipitation method. The obtained precipitate was calcined at500, 700,900and 1000°С. Phase characterization of synthesized LSCF and LDySCF powder before and after heat treatment at 700°Сwas carried out by X-ray diffraction (XRD) analysis. XRD patterns revealed that the perovskite phase was obtained at 700 °С in all calcined samples. Chemical bond study to investigate synthesis process was done using the Fourier transform infrared spectroscopy technique. Thermalanalysis of DTA and TG has been utilized to investigate how the calcination temperature affects the peroveskite phase formation. According to the STA results, the perovskite phase formation started at 551°Сafterwarditcompleted at 700°С.The density values of synthesized powders were 6.10, 6.11 and 6.37g.cm-3for the undoped and doped samples calcined at 700°С. Powder morphology was studied by Field emission scanning electron microscopy. (FE-SEM) micrographs showed the spherical shaped particles with the average particle size of 24-131nm.

Synthesis Mechanism and Microstructure Characterization of BaIn2O4

2011 ◽  
Vol 347-353 ◽  
pp. 1342-1347 ◽  
Author(s):  
Ping Ren ◽  
Li Cheng Zhou ◽  
Jun Xi Zhang ◽  
Hong Yun
Keyword(s):  
Sintering Temperature ◽  
Precipitation Method ◽  
Sintering Process ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Synthesis Mechanism ◽  
X Ray ◽  
Grain Sizes ◽  
Co Precipitation

The synthesis mechanism and microstructures of BaIn2O4 particles were analyzed by simultaneous thermogravimetry - differential scanning calorimetry (TG-DSC), X-ray diffraction (XRD), and scanning electron microscope (SEM). Firstly, In(OH)3 and BaCO3 precursors were prepared by the co-precipitation method. Next, during the sintering process In(OH)3 initially decomposed into In2O3 and water, and then BaCO3 reacted with In2O3 to synthesize Ba4In6O13. Finally, Ba4In6O13 and In2O3 further reacted to form BaIn2O4. The obtained BaIn2O4 particles were in monoclinic structure and exhibited high crystal quality. The grains were tightly bound together and their boundaries became blurry. The grain sizes increased with increasing the sintering temperature.

Exploring the characterization of Ni doped MgO nanoparticles using co-precipitation method

2020 ◽  
Vol 3 (1) ◽  
pp. 30-33
Author(s):  
Muthulakshmi M ◽  
Madhumitha G
Keyword(s):  
Magnesium Oxide ◽  
Analytical Techniques ◽  
Nickel Chloride ◽  
Precipitation Method ◽  
Crystalline Powder ◽  
High Melting Point ◽  
Design Synthesis ◽  
Mgo Nanoparticles ◽  
Co Precipitation

Nanotechnology is a field of applied science focused on design, synthesis and characterization of nanomaterials. The nickel and magnesium have improved their applications in transparent electrodes and nano electronics. In addition, magnesium oxide has moisture resistance and high melting point properties. In the present work has been carried out in the development of green crystalline powder of nickel doped magnesium oxide nanoparticles by Co-precipitation method, from the mixture of nickel chloride and magnesium chloride with KOH as solvent. From the XRD results, crystalline size of the particle can be observed. Spherical structure of Ni doped MgO nanoparticles were indicated by SEM results and powdered composition of samples were obtained from FTIR. EDAX represents the peak composition of the nanoparticle. The above analytical techniques have confirmed that the Ni doped MgO nanoparticles obtained from the mixture of NiCl2 and MgCl2.

Microstructure Characterization of Metal Mixed Oxides

MRS Advances ◽  
2017 ◽  
Vol 2 (64) ◽  
pp. 4025-4030 ◽  
Author(s):  
T. Kryshtab ◽  
H. A. Calderon ◽  
A. Kryvko
Keyword(s):  
Mixed Oxides ◽  
Profile Analysis ◽  
Atomic Resolution ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
Reconstruction Procedure ◽  
Transmission Electron ◽  
Xrd Patterns ◽  
Co Precipitation

ABSTRACTThe microstructure of Ni-Mg-Al mixed oxides obtained by thermal decomposition of hydrotalcite-like compounds synthesized by a co-precipitation method has been studied by using X-ray diffraction (XRD) and atomic resolution transmission electron microscopy (TEM). XRD patterns revealed the formation of NixMg1-xO (x=0÷1), α-Al2O3 and traces of MgAl2O4 and NiAl2O4 phases. The peaks profile analysis indicated a small grain size, microdeformations and partial overlapping of peaks due to phases with different, but similar interplanar spacings. The microdeformations point out the presence of dislocations and the peaks shift associated with the presence of excess vacancies. The use of atomic resolution TEM made it possible to identify the phases, directly observe dislocations and demonstrate the vacancies excess. Atomic resolution TEM is achieved by applying an Exit Wave Reconstruction procedure with 40 low dose images taken at different defocus. The current results suggest that vacancies of metals are predominant in MgO (NiO) crystals and that vacancies of Oxygen are predominant in Al2O3 crystals.

Magnetic and morphological characterization of Bi2Fe4O9 nanoparticles synthesized via a new reverse chemical co-precipitation method

2017 ◽  
Vol 43 (15) ◽  
pp. 12120-12125 ◽  
Author(s):  
S.A.N.H. Lavasani ◽  
O. Mirzaee ◽  
H. Shokrollahi ◽  
A.K. Moghadam ◽  
M. Salami
Keyword(s):  
Morphological Characterization ◽  
Precipitation Method ◽  
Co Precipitation

Effect of the Synthesis Method on the Properties of Ultrafine YAG Powder

2018 ◽  
Vol 281 ◽  
pp. 40-45
Author(s):  
Jie Guang Song ◽  
Lin Chen ◽  
Cai Liang Pang ◽  
Jia Zhang ◽  
Xian Zhong Wang ◽  
...  
Keyword(s):  
Particle Size ◽  
Calcination Temperature ◽  
Hydrothermal Reaction ◽  
Synthesis Method ◽  
Particle Morphology ◽  
Precipitation Method ◽  
Molar Ratio ◽  
Synthesis Process ◽  
Powder Materials ◽  
Co Precipitation

YAG materials has a number of unique properties, the application is very extensive. In this paper, the superfine YAG powder materials were prepared by co-precipitation method and hydrothermal precipitation method. The influence of synthesis process on the morphology of the powder was investigated. The results showed that the precursor powder prepared via the co-precipitation method is mainly from amorphous to crystalline transition with the increasing calcination temperature, the precursor agglomeration is more serious, In the process of increasing the calcination temperature, the dispersibility of the roasted powder is greatly improved, which is favorable for the growth of the crystal grains, so that the particle size of the powder is gradually increased, the YAG precursor prepared by the co-precipitation method is transformed into YAG crystals, the phase transition occurs mainly between 900 and 1100°C. When the molar ratio of salt to alkali is Y3+: OH-=1: 8 via the hydrothermal reaction, the YAG particles with homogeneous morphology can be obtained. When the molar ratio of salt and alkali is increased continuously, the morphology of YAG particles is not obviously changed. The co-precipitation method is easy to control the particle size, the hydrothermal method is easy to control the particle morphology.

Fabrication and characterization of collagen–hydroxyapatite-based composite scaffolds containing doxycycline via freeze-casting method for bone tissue engineering

2018 ◽  
Vol 33 (4) ◽  
pp. 501-513 ◽  
Author(s):  
Hossein Semyari ◽  
Majid Salehi ◽  
Ferial Taleghani ◽  
Arian Ehterami ◽  
Farshid Bastami ◽  
...  
Keyword(s):  
Cellular Response ◽  
Composite Scaffold ◽  
Precipitation Method ◽  
Structural Isomer ◽  
Freeze Casting ◽  
Hydroxyapatite Nanoparticles ◽  
Casting Method ◽  
Defect Model ◽  
Co Precipitation

In this study, hydroxyapatite nanoparticles containing 10% doxycycline, a structural isomer of tetracycline, was prepared by the co-precipitation method. It was added to collagen solution for the preparation of the scaffold with freeze-casting method in order to develop a composite scaffold with both antibacterial and osteoinductive properties for repairing bone defects. The scaffolds were evaluated regarding their morphology, porosity, degradation and cellular response. The scaffolds for further investigation were added in a rat calvaria defect model. The study showed that after eight weeks, the bone formation was relatively higher in the collagen/nano-hydroxyapatite/doxycycline group with completely filled defect when compared with other groups. Histopathological evaluation showed that the defect in the collagen/nano-hydroxyapatite/doxycycline group was fully replaced by the new bone and connective tissue. Our results provide evidence supporting the possible applicability of doxycycline-containing scaffolds for successful bone regeneration.

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