Synthesis of Powders Nanometer Al2O3 Method by Sol-Gel

2012 ◽  
Vol 727-728 ◽  
pp. 9-13
Author(s):  
Suzana Arleno S. Santos ◽  
Eduardo Sousa Lima ◽  
Luis Henrique Leme Louro ◽  
Célio Albano da Costa
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Particle Size ◽  
Thermogravimetric Analysis ◽  
Calcination Temperature ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Average Size ◽  
Scanning Electron

This study aimed to produce nanometric powders of alumina by sol-gel route. Six samples were produced by varying the amount of water for dilution of aluminum nitrate and the calcination temperature. The final products were evaluated by thermogravimetric analysis, scanning electron microscopy, X-ray diffraction and particle size. It could be noticed that, beyond the time of gelation and calcination temperature, the addition of water also influenced the average size of the clusters.

scholarly journals Structural and optical properties of SnO2–Al2O3 nanocomposite synthesized via sol-gel route

2015 ◽  
Vol 33 (4) ◽  
pp. 714-718 ◽  
Author(s):  
Neeraj K. Mishra ◽  
Chaitnaya Kumar ◽  
Amit Kumar ◽  
Manish Kumar ◽  
Pratibha Chaudhary ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Optical Properties ◽  
Sol Gel ◽  
Physical Interaction ◽  
X Ray Diffraction ◽  
Structural And Optical Properties ◽  
X Ray ◽  
Sensing Applications ◽  
Scanning Electron

AbstractA nanocomposite of 0.5SnO2–0.5Al2O3 has been synthesized using a sol-gel route. Structural and optical properties of the nanocomposite have been discussed in detail. Powder X-ray diffraction and scanning electron microscopy with energy-dispersive X-ray diffraction spectroscopy confirm the phase purity and the particle size of the 0.5SnO2–0.5Al2O3 nanocomposite (13 to 15 nm). The scanning electron microscopy also confirms the porosity in the sample, useful in sensing applications. The FT-IR analysis confirms the presence of physical interaction between SnO2 and Al2O3 due to the slight shifting and broadening of characteristic bands. The UV-Vis analysis confirms the semiconducting nature because of direct transition of electrons into the 0.5SnO2–0.5Al2O3 nanocomposites.

Preparation of Borosilicate Xerogel and Research on its Mineralization

2012 ◽  
Vol 476-478 ◽  
pp. 2059-2062
Author(s):  
Chen Wang ◽  
Ya Dong Li ◽  
Gu Qiao Ding
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Fourier Transform ◽  
Infrared Spectroscopy ◽  
Ph Value ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Compositional Changes ◽  
Scanning Electron

Tributyl borate was first adopted for the introduction of boron in the preparation of bioactive borosilicate xerogel by sol-gel method. The xerogel reacted continuously in 0.25M K2HPO4 solution with a starting pH value of 7.0 at 37 °C for 1day. The structural, morphologies and compositional changes resulting from the conversion were characterized using X-ray diffraction, scanning electron microscopy and Fourier transform infrared spectroscopy. The results indicated that speed of formation of HA was cut way back on the time with the addition of boron and the induction period for the HA nucleation on the surface of the borosilicate xerogel was short than 1 days. The conversion mechanism of the borosilicate xerogels to hydroxyapaptite was also discussed.

scholarly journals Synthesis of Brushite from Phophogypsum Industrial Waste

2021 ◽  
Vol 12 (5) ◽  
pp. 6580-6588
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Industrial Waste ◽  
Sol Gel ◽  
Dicalcium Phosphate Dihydrate ◽  
X Ray Diffraction ◽  
Characterization Methods ◽  
X Ray ◽  
Phosphate Dihydrate ◽  
Scanning Electron

Dicalcium phosphate dihydrate (DCPD) nanoparticles, also known as brushite, are considered an important bioceramic compound. In this study, brushite was prepared from Moroccan phosphogypsum (PG) using a new sol-gel method. A two-step technique undergoes the synthesis of brushite, the preparation of anhydrite from PG followed by adding phosphoric acid in the presence of sodium hydroxide. The morphology, the chemical composition, and the crystallites size were obtained using Scanning Electron Microscopy (SEM-EDAX), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR), respectively. According to the Debye-Scherrer equation, these characterization methods indicated that the synthesized brushite was highly pure according to the Ca/P ratio of 1.14 and an average crystallites size estimated at 66 nm. These results proved that the brushite was successfully synthesized from Moroccan phosphogypsum.

Biomorphic SiC Prepared from Carbonized Millet by Sol-Gel and Carbothermal Reduction Processing

2010 ◽  
Vol 152-153 ◽  
pp. 1683-1686
Author(s):  
Qing Wang ◽  
Ya Hui Zhang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Silicon Carbide ◽  
Phase Composition ◽  
Carbothermal Reduction ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carbon Template ◽  
Scanning Electron

Biomorphic silicon carbide (bioSiC) was prepared by high temperature pyrolysis and sol-gel and carbothermal reduction processing at 1600 oC. The morphology and microstructure of carbon-silica composites and purified bioSiC samples were characterized by scanning electron microscopy. The phase composition of the resulting sample was analyzed by X-ray diffraction. The results suggest that the bioSiC mainly consists of cubic ß-SiC, and principally replicates the shape and microstructure of the carbon template.

SiO2ZrO2 Thin Films as Low Temperature NO2 and O3 Sensors

2015 ◽  
Vol 1088 ◽  
pp. 81-85 ◽  
Author(s):  
T.N. Myasoedova ◽  
Victor V. Petrov ◽  
Nina K. Plugotarenko ◽  
Dmitriy V. Sergeenko ◽  
Galina Yalovega ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thin Films ◽  
Scanning Electron Microscopy ◽  
Low Temperature ◽  
Annealing Temperature ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Operating Temperatures ◽  
Scanning Electron

Thin SiO2ZrO2films were prepared, up to 0.2 μm thick, by means of the sol–gel technology and characterized by a Scanning electron microscopy and X-ray diffraction. It is shown the presence of monoclinic, cubic and tetragonal phases of ZrO2in the SiO2matrix. The crystallites sizes depend on the annealing temperature of the film and amount to 35 and 56 nm for the films annealed at 773 and 973 K, respectively. The films resistance is rather sensitive to the presence of NO2and O3impurity in air at lower operating temperatures in the range of 30-60°C.

Biomorphic TiO2 Ceramics Prepared from Cotton Stalk

2012 ◽  
Vol 602-604 ◽  
pp. 526-529
Author(s):  
Qing Wang ◽  
Lin Zhang ◽  
Ya Hui Zhang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Phase Composition ◽  
High Temperature ◽  
Sol Gel ◽  
Cotton Stalk ◽  
X Ray Diffraction ◽  
X Ray ◽  
Carbon Template ◽  
Scanning Electron

Biomorphic TiO2 was prepared by high temperature pyrolysis and a modified sol-gel route. The morphology and microstructure of TiO2 samples were characterized by scanning electron microscopy. The phase composition of the resulting sample was analyzed by X-ray diffraction. The results suggest that the biomorphic TiO2 mainly consists of rutile TiO2, and replicates the shape and part microstructure of the carbon template.

Synthesis of Triethynylborazine-Polyhydromethylsiloxane Copolymers and its Ceramization

2013 ◽  
Vol 774-776 ◽  
pp. 629-633
Author(s):  
Ji Feng Jiang ◽  
Kang Kang Guo ◽  
Ya Ping Zhu ◽  
Fan Wang ◽  
Hui Min Qi
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Nuclear Magnetic Resonance ◽  
Fourier Transform ◽  
Thermogravimetric Analysis ◽  
X Ray Diffraction ◽  
Hydrosilylation Reaction ◽  
X Ray ◽  
Ft Ir ◽  
Scanning Electron

Triethynylborazine-polyhydromethylsiloxane copolymers (TEB-PHMSs) were prepared through hydrosilylation reaction between -C≡CH attached to boron and ≡Si-H. The structures of TEB-PHMSs were characterized by Fourier transform Infrared (FT-IR) and Nuclear Magnetic Resonance (NMR) spectroscopy. Their cure behavior were examined by Differential Scanning Calorimeter (DSC) and FT-IR, and then thermostability and ceramization of cured TEB-PHMS were investigated by Thermogravimetric analysis (TGA), pyrolysis-GC-MS, X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM). The results indicated that TEB-PHMSs could be cured and converted into an outstanding thermostable SiBCN ceramics.

Preparation and Properties of CaF2 Nano-Powder

2016 ◽  
Vol 680 ◽  
pp. 257-260
Author(s):  
Meng Yun Dong ◽  
Cheng Zhang ◽  
Jin Feng Xia ◽  
Hong Qiang Nian ◽  
Dan Yu Jiang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Particle Size ◽  
Sintering Temperature ◽  
Raw Materials ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nano Powder ◽  
Direct Precipitation ◽  
Scanning Electron

CaF2 nano-power was prepared by direct precipitation methods with Ca(NO3)2 and KF as raw materials. The influences of presintering temperature and sintering temperature on the particle size and distribution of CaF2 nano-power were studied by X-ray diffraction (XRD) and field-emission scanning electron microscopy (FESEM). This study provided an experimental method for preparation of CaF2 nano-power. The results show that the best presintering temperature of CaF2 nano-power is 500°C and the best sintering temperature of CaF2 ceramic is 900°C.

CYCLIC IMPROVEMENT OF LiNi0.5Mn1.5O4 POLYHEDRAL SPINELS FOR 5.0 V LITHIUM ION BATTERIES

2010 ◽  
Vol 03 (03) ◽  
pp. 185-188 ◽  
Author(s):  
XIAOYUN ZHAN ◽  
ZHAOHUI LI ◽  
JIAOJUN TANG ◽  
QIZHEN XIAO ◽  
GANGTIE LEI ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Particle Size ◽  
Lithium Ion ◽  
Electrochemical Measurement ◽  
Cycling Performance ◽  
Small Particle Size ◽  
X Ray Diffraction ◽  
X Ray ◽  
Scanning Electron

Highly crystallized and microsized particles of LiNi0.5Mn1.5O4 spinels with different morphologies have been successfully synthesized using polystyrene (PS) as the sacrificial template, and were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and electrochemical measurement. The spinels obtained at 700°C possess abundant porosity with about 200 nm in diameter, while the spinels calcined at 900°C exhibit a well-defined polyhedral morphology with particle size ranged from 0.2 to 2 μm. The materials prepared at 900°C display an excellent cycling performance due probably to better crystallinity and small particle size.

X-ray powder diffraction data for two new compounds (NH4)1.5Ni2V2O7(OH)1.5 · H2O and (NH4)1.5Cu1.125Ni1.125V2O7(OH)2 · H2O

2011 ◽  
Vol 26 (S1) ◽  
pp. S51-S54
Author(s):  
Johana Arboleda ◽  
Adriana Echavarría
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Thermogravimetric Analysis ◽  
Powder Diffraction ◽  
Diffraction Data ◽  
Powder Diffraction Data ◽  
X Ray Diffraction ◽  
X Ray ◽  
New Compounds ◽  
Scanning Electron

Two new bimetallic and trimetallic compounds (NH4)1.5Ni2V2O7(OH)1.5 · H2O and (NH4)1.5Cu1.125 Ni1.125V2O7(OH)2 · H2O were synthesized by hydrothermal method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and X-Ray fluorescence (XRF). Crystallographic studies showed that both compounds are hexagonal with space group P-62c.

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