Synthesis and Characterization of Nanocrystalline SnO2 Powder

2011 ◽  
Vol 675-677 ◽  
pp. 267-270
Author(s):  
Shi Min Liu ◽  
Wan Yu Ding ◽  
Wei Wei Jiang ◽  
Wei Ping Chai
Keyword(s):  
Morphological Properties ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Direct Precipitation ◽  
Transmission Electron ◽  
Crystal Structural ◽  
Sno2 Powder ◽  
Direct Precipitation Method

Nanocrystalline SnO2 powder has been synthesized via direct precipitation method starting from Sn, HNO3, HCl, and NH4OH. Thermal properties, crystal structural and morphological properties of the precursor and SnO2 powder were investigated using simultaneous thermogravimetry-differential thermal analysis, X-ray diffraction and transmission electron microscopy. The results indicated that the precursor was SnO2 rather than Sn(OH)2 or Sn(OH)4. On the basis of the precursor, well crystallized SnO2 powder with 4-5 nm in diameter was obtained, after calcined at 350 °C for 2 h.

Synthesis and Characterization of Structure of Fe3O4@Graphene Oxide Nanocomposites

2016 ◽  
Vol 25 (6) ◽  
pp. 096369351602500 ◽  
Author(s):  
Ruimin Fu ◽  
Mingfu Zhu
Keyword(s):  
Graphene Oxide ◽  
Drug Carrier ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Ft Ir ◽  
Co Precipitation ◽  
Ft Ir Spectroscopy

Nowadays, the hummers method for preparation of graphene oxide (GO) was improved. The grapheme oxide @ Fe3O4 magnetic nanocomposites were synthesized by co-precipitation method. After analysing the morphology and structure of obtained nanocomposites by X-ray diffraction (XRD), transmission electron microscope (TEM) and Fourier transform infrared (FT-IR) spectroscopy, the result was shown as follows. The particle size of Fe3O4 in nanocomposites is 30 nm. Many functional groups are found in grapheme oxide, and such groups could be used to bind with the drug. In the test for magnetic properties, the nanocomposites gathered rapidly in the vicinity of the permanent magnet. The nanocomposites, with high superparamagnetism, can be used in the following applications: drug targeting transports, drug carrier, and diagnosis assistant system.

Characterization of two forms of sepiolite and related Mg-rich clay minerals from Yenidoğ an (Sivrihisar, Turkey)

Clay Minerals ◽  
2014 ◽  
Vol 49 (1) ◽  
pp. 91-108 ◽  
Author(s):  
M. Yeniyol
Keyword(s):  
Field Work ◽  
Ion Concentration ◽  
Morphological Properties ◽  
Chemical Analyses ◽  
X Ray Diffraction ◽  
X Ray ◽  
Direct Precipitation ◽  
Extensive Field ◽  
Sedimentary Succession

AbstractAn Early Pliocene sedimentary succession in the Yenidoğan area, Sivrihisar, Turkey, consists of sepiolite, stevensite, kerolite, dolomite and magnesite. The geology, mineralogy and geochemistry of the succession was examined by extensive field work along several trenches and a representative measured section, followed by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), thermal, and chemical analyses.Structurally, two distinct forms of sepiolites were distinguished by XRD: (a) well crystallized sepiolite with a 110 reflection at 12.07–12.3 Å , and (b) poorly crystallized sepiolite in which the 110 reflection occurs at 12.7–13.0 Å (denoted as sepiolite-13Å ). Differences in crystal chemistry, thermal and morphological properties of these forms, the vibrational spectra and XRD characterization of the related phyllosilicates were also documented.Stevensite, kerolite and sepiolite were formed by direct precipitation from alkaline lake water rich in Mg and Si. Sepiolite-13Å was probably formed by transformation from precursor smectite via dissolution-precipitation, more likely during early diagenesis. Environmental conditions such as ion concentration, salinity and variations in pH may have controlled the formation of the phyllosilicates.

Preparation and Characterization of Fibrous Hydroxyapatite/Chitosan Nanocomposites with High Hydroxyapatite Dosage

2012 ◽  
Vol 457-458 ◽  
pp. 365-371 ◽  
Author(s):  
Cai Yun Zhang ◽  
Dai Yin Peng ◽  
Chuan Hua Lu ◽  
Xian Ping Wang ◽  
Qian Feng Fang
Keyword(s):  
Morphological Properties ◽  
In Vitro Tests ◽  
X Ray Diffraction ◽  
Permeable Membrane ◽  
X Ray ◽  
Chitosan Matrix ◽  
Transmission Electron

In this paper the hydroxyapatite fibers reinforced chitosan nanocomposites with high hydroxyapatite dosage (70~90 wt%) were synthesized by in-situ hybridization. The semi-permeable membrane was used to control the process of hybridization and morphology of hydroxyapatite. The compositional and morphological properties of nanocomposites were investigated by FTIR spectroscopy, X-ray diffraction, and transmission electron microscopy. The results showed that the hydroxyapatite were carbonated nanometer crystalline fibers with high aspect ratio (about 25) and dispersed uniformly in the nanocomposites. The high-resolution image indicated that the growth of nano-hydroxyapatite crystallites in the chitosan matrix preferred in the c-axis. The mechanical properties of these nanocomposites were enhanced dramatically and the compressive strength increases almost to 170MPa when the hydroxyapatite content is 70 wt%. The in vitro tests indicated that the composites have high bioactivity and degradation. These properties illustrated the potential application of this kind of nanocomposites for bone tissue engineering.

Characterization of Al2(WO4)3 Synthesized by Co-Precipitation Method

2014 ◽  
Vol 798-799 ◽  
pp. 85-89 ◽  
Author(s):  
E.S.G. Junior ◽  
P.M . Jardim
Keyword(s):  
Precipitation Method ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Tem Analysis ◽  
X Ray ◽  
Transmission Electron ◽  
Different Temperatures ◽  
Co Precipitation ◽  
Alpha Alumina

Al2(WO4)3was synthesized by co-precipitation using Na2WO4and Al (NO3)3as precursors. After drying the precipitate, it was calcined at different temperatures between 500°C and 800°C. The crystallization and degradation temperatures of the samples were evaluated by means of Differential Scanning Calorimetry (DSC), Thermogravimetry (TG) and X-Ray Diffraction (XRD). It was observed that the crystallization starts at around 600°C, however Transmission Electron Microscopy (TEM) analysis showed that at this temperature the sample is partially amorphous. The degradation of the material starts at around 1200°C and at 1400°C the tungsten oxide has almost completely evaporated and the material is transformed mainly in alpha-alumina.

SYNTHESIS AND CHARACTERIZATION OF α-Fe2O3@ATO NANOCOMPOSITE PARTICLES

2008 ◽  
Vol 15 (05) ◽  
pp. 545-550 ◽  
Author(s):  
YIN-CUN ZHU ◽  
JI-SEN JIANG
Keyword(s):  
Weight Ratio ◽  
Precipitation Method ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Nanocomposite Particles ◽  
X Ray ◽  
Homogeneous Precipitation Method ◽  
Treatment Conditions ◽  
Transmission Electron

α- Fe 2 O 3@ATO (antimony doped tin oxide) nanocomposite particles with core–shell structure were prepared by homogeneous precipitation method using monodispersed α- Fe 2 O 3 (hematite) nanoparticles as cores, SnCl 4 · 5 H 2 O and SbCl 3 as the precursor of the shell. The morphology and structure of the nanocomposite particles were studied with transmission electron microscopy and X-ray diffraction, respectively. The electricity properties of the nanocomposite were also investigated in terms of coating amount, molar ratio of element Sb to Sn , and heat treatment conditions. The results showed that the conditions of ATO/α- Fe 2 O 3 (weight ratio) = 70%, n( Sb )/n( Sn ) = 10%, calcined at 700°C for 1 h were optimal for the conductivity of the nanocomposite.

Synthesis and Characterization of Fe and Fe2O3 Nanoparticles

2013 ◽  
Vol 678 ◽  
pp. 46-49 ◽  
Author(s):  
Ponnaian Peula Kumari ◽  
Rachel Oommen ◽  
Chinna Kannaiyan Senthil Kumaran ◽  
Mariyappan Thambidurai ◽  
Natarajan Muthukumarasamy ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Secondary Phase ◽  
Chemical Precipitation ◽  
Precipitation Method ◽  
Synthesis And Characterization ◽  
Cubic Phase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron

Fe and Fe2 O3 nanoparticle have been synthesized by chemical precipitation method. The x-ray diffraction studies indicate the formation of Fe and Fe2 O3 nanoparticles with cubic phase and no secondary phase was observed. Surface morphology of Fe and Fe2 O3 has been studied using scanning electron microscopy (SEM). Transmission electron microscopy (TEM) images reveal that Fe and Fe2 O3 nanoparticle have size ranging from 25-41 nm.

Fabrication and Characterization of Hollow Zirconia Microspheres Using Calcium Carbonate as Template

2016 ◽  
Vol 230 (11) ◽  
Author(s):  
Shengsong Ge ◽  
Weixue Zhu ◽  
Qian Shao
Keyword(s):  
Calcium Carbonate ◽  
Nitrogen Adsorption ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Fabrication And Characterization ◽  
Adsorption Desorption ◽  
Spherical Hollow

AbstractStabilized spherical hollow zirconia was fabricated using calcium carbonate as template through a simple precipitation method. The as-prepared products were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscope (TEM) and nitrogen adsorption–desorption isotherms (BET). Adsorption performance of the as-prepared products toward Congo red (CR) aqueous solutions was tested and discussed. Results show that the prepared hollow ZrO

The Use of Advanced Analytical Techniques for Characterization of the Chemical, Physical, and Crystallographic Nature of a Surface

1973 ◽  
Vol 31 ◽  
pp. 132-133 ◽  
Author(s):  
R. E. Herfert
Keyword(s):  
Surface Characterization ◽  
Analytical Techniques ◽  
X Ray Diffraction ◽  
Depth Of Penetration ◽  
X Ray ◽  
The Past ◽  
Transmission Electron ◽  
Scanning Electron

Studies of the nature of a surface, either metallic or nonmetallic, in the past, have been limited to the instrumentation available for these measurements. In the past, optical microscopy, replica transmission electron microscopy, electron or X-ray diffraction and optical or X-ray spectroscopy have provided the means of surface characterization. Actually, some of these techniques are not purely surface; the depth of penetration may be a few thousands of an inch. Within the last five years, instrumentation has been made available which now makes it practical for use to study the outer few 100A of layers and characterize it completely from a chemical, physical, and crystallographic standpoint. The scanning electron microscope (SEM) provides a means of viewing the surface of a material in situ to magnifications as high as 250,000X.

Detonation Synthesis of Nano-Size Materials

1995 ◽  
Vol 418 ◽  
Author(s):  
J. Forbes ◽  
J. Davis ◽  
C. Wong
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Nucleation And Growth ◽  
Detonation Synthesis ◽  
X Ray Diffraction ◽  
Crystalline Materials ◽  
X Ray ◽  
Transmission Electron ◽  
Nano Size

AbstractThe detonation of explosives typically creates 100's of kbar pressures and 1000's K temperatures. These pressures and temperatures last for only a fraction of a microsecond as the products expand. Nucleation and growth of crystalline materials can occur under these conditions. Recovery of these materials is difficult but can occur in some circumstances. This paper describes the detonation synthesis facility, recovery of nano-size diamond, and plans to synthesize other nano-size materials by modifying the chemical composition of explosive compounds. The characterization of nano-size diamonds by transmission electron microscopy and electron diffraction, X-ray diffraction and Raman spectroscopy will also be reported.

One Step Synthesis and Characterization of Zirconia-Graphene Composites

2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  
Keyword(s):  
Synthesis And Characterization ◽  
Two Dimensional ◽  
X Ray Diffraction ◽  
X Ray ◽  
Graphene Composite ◽  
Transmission Electron ◽  
One Step ◽  
Ft Ir ◽  
Xrd Techniques

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.

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