scholarly journals Surface morphology and particle size analysis of Ba0.5Sr0.5TiO3 nano-powder grown using sol-gel method

Author(s):  
R. Balachandran ◽  
H.K. Yow ◽  
B.H. Ong ◽  
K. Anuar ◽  
W.T. Teoh ◽  
...  
2019 ◽  
Vol 7 (17) ◽  
pp. 4981-4987 ◽  
Author(s):  
Ruiyu Bao ◽  
Chen Chen ◽  
Jianxin Xia ◽  
Huiying Chen ◽  
Hua Li

The surface morphology and particle size of materials can be controlled using DEP technology.


1994 ◽  
Vol 346 ◽  
Author(s):  
Manzheng Ge ◽  
Honghua Kan ◽  
Hui Yang ◽  
Jianmin Qiao ◽  
Zhonghua Jiang

ABSTRACTThe Y2O3-La2O3 additive-coated Si3N4 powders of about 1.5 μm in size were prepared by the sol-gel method. X-ray diffraction, X-ray photoelectron spectroscopy, differential thermal analysis, thermogravimetric analysis, electron microscopies, and particle size analysis were used to study the coating on the Si3N4 particles. The results show that properties of the bulk Si3N4 powder are not affected by using the sol-gel coating and the powders are homogeneously coated by a thin layer of the Y2O3-La2O3 additives. The structure of the Y2O3-La2O3 coating layer is amorphous or microcrystalline with a submicron thickness. The coated powders are then more sinterable, and the mechanical properties of the ceramics prepared from such powders are improved.


2013 ◽  
Vol 756 ◽  
pp. 91-98 ◽  
Author(s):  
Ftema W. Aldbea ◽  
Noor Bahyah Ibrahim ◽  
Mustafa Hj. Abdullah

Terbium –substituted yttrium iron garnet (Tb1.5Y1.5Fe5O12) films nanoparticles were successfully prepared by a sol-gel method. The films were deposited on the quartz substrate using spin coating technique. To study effect of annealing temperature, the annealing process was executed at 700, 800 and 900 °C in air for 2 hours. The X-ray diffraction (XRD) proved that the pure phase of garnet structure was detected for the film annealed at 900 °C. The lattice parameter increased with the increment of annealing temperature and the highest value of 12.35 Å was obtained at 900 °C. Field Emission Scanning Electron Microscope (FE-SEM) results showed that the particle size increased from 43nm to 56nm as annealing temperature increased from 700 to 900°C. The film’s thickness also affected by increasing of annealing temperature and become thin at 900 °C due to densification process occurred at high annealing temperature. The elemental compositions of the Tb1.5Y1.5Fe5O12 film were detected using an Energy Dispersive X-raySpectroscopy (EDX). Magnetic properties at room temperature were measured using a Vibrating Sample Magnetometer (VSM).The saturation magnetization Ms increased with the annealingtemperature and showed a high value of 104emu/cm3, but the coercivity Hc of the film was decreased due to the increment of the particle size. Normal 0 21 false false false MS X-NONE X-NONE MicrosoftInternetExplorer4 Terbium –substituted yttrium iron garnet (Tb1.5Y1.5Fe5O12) films nanoparticles were successfully prepared by a sol-gel method. The films were deposited on the quartz substrate using spin coating technique. To study effect of annealing temperature, the annealing process was executed at 700, 800 and 900°C in air for 2 hours. The X-ray diffraction (XRD) proved that the pure phase of garnet structure was detected for the film annealed at 900 °C. The lattice parameter increased with the increment of annealing temperature and the highest value of 12.35 Å was obtained at 900 °C. Field Emission Scanning Electron Microscope (FE-SEM) results showed that the particle size increased from 43nm to 56nm as annealing temperature increased from 700 to 900 °C. The film’s thickness also affected by increasing of annealing temperature and become thin at 900 °C due to densification process occurred at high annealing temperature. The elemental compositions of the Tb1.5Y1.5Fe5O12 film were detected using an Energy Dispersive X-ray Spectroscopy (EDX). Magnetic properties at room temperature were measured using a Vibrating Sample Magnetometer (VSM).The saturation magnetization Ms increased with the annealing temperature and showed a high value of 104emu/cm3, but the coercivity Hc of the film was decreased due to the increment of the particle size. st1\:*{behavior:url(#ieooui) } /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal"; mso-tstyle-rowband-size:0; mso-tstyle-colband-size:0; mso-style-noshow:yes; mso-style-priority:99; mso-style-qformat:yes; mso-style-parent:""; mso-padding-alt:0cm 5.4pt 0cm 5.4pt; mso-para-margin:0cm; mso-para-margin-bottom:.0001pt; mso-pagination:widow-orphan; font-size:11.0pt; font-family:"Calibri","sans-serif"; mso-ascii-font-family:Calibri; mso-ascii-theme-font:minor-latin; mso-fareast-font-family:"Times New Roman"; mso-fareast-theme-font:minor-fareast; mso-hansi-font-family:Calibri; mso-hansi-theme-font:minor-latin; mso-bidi-font-family:"Times New Roman"; mso-bidi-theme-font:minor-bidi;}


2011 ◽  
Vol 10 (2) ◽  
pp. 25
Author(s):  
Anirut Leksomboon ◽  
Bunjerd Jongsomjit

In this present study, the spherical silica support was synthesized from tetraethyloxysilane (TEOS), water, sodium hydroxide, ethylene glycol and n-dodecyltrimethyl ammonium bromide (C12TMABr). The particle size was controlled by variation of the ethylene glycol co-solvent weight ratio of a sol-gel method preparation in the range of 0.10 to 0.50. In addition, the particle size apparently increases with high weight ratio of co-solvent, but the particle size distribution was broader. The standard deviation of particle diameter is large when the co-solvent weight ratio is more than 0.35 and less than 0.15. However, the specific surface area was similar for all weight ratios ranging from 1000 to 1300 m2/g. The synthesized silica was spherical and has high specific surface area. The cobalt was impregnated onto the obtained silica to produce the cobalt catalyst used for CO2 hydrogenation.</


2013 ◽  
Vol 712-715 ◽  
pp. 257-261
Author(s):  
Yin Lin Wu ◽  
Qing Hui Wang ◽  
Ling Wang ◽  
Hai Yan Zhao

The La0.75Sr0.25Cr0.5Mn0.5O3-δnanometer powders were prepared by citric acid sol-gel method.The samples were characterized by DTA, FT-IR, XRD, TEM techniques. The preparation process, morphology of synthesized powders, the best heat-treatment temperature and the electrochemical performance had been studied. The results show that the spherical nanometer powders can be obtained and the best heat-treatment temperature is 800°C. The particle size is about 30nm and Ea is 0.071 eV.


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Anna Prnová ◽  
Jana Valúchová ◽  
Monika Michálková ◽  
Beáta Pecušová ◽  
Milan Parchovianský ◽  
...  

Abstract Glass microspheres with yttria-alumina eutectic composition (76.8 mol % Al2O3 and 23.2 mol % Y2O3) were prepared by sol-gel Pechini method and flame synthesis with or without subsequent milling. Prepared amorphous powders were studied by X-ray powder diffraction (XRD), particle size analysis (PSA), scanning electron microscopy (SEM) and differential thermal analysis (DTA). Hot pressing (HP), rapid hot pressing (RHP) and spark plasma sintering (SPS) were used to sinter amorphous precursor powders at 1600 °C without holding time (0 min). The preparation process including milling step resulted in amorphous powders with narrower particle size distribution and smaller particle size. All applied pressure assisted sintering techniques resulted in dense bulk samples with fine grained microstructure consisting of irregular α-Al2O3 and Y3Al5O12 (YAG) grains. Milling was beneficial in terms of final microstructure refinement and mechanical properties of sintered materials. A material with the Vickers hardness of HV = (17.1 ± 0.3) GPa and indentation fracture resistance of (4.2 ± 0.2) MPa.m1/2 was prepared from the powder milled for 12 h.


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