Synthesis and Characterization of Monodisperse Magnetite Nanoparticles by Hydrothermal Method

2017 ◽  
Vol 737 ◽  
pp. 367-372
Author(s):  
Apichon Watcharenwong ◽  
Yotsapon Bailuang ◽  
Puangrat Kajitvichyanukul
Keyword(s):  
Electron Microscope ◽  
Saturation Magnetization ◽  
Hydrothermal Method ◽  
Magnetite Nanoparticles ◽  
Hysteresis Loops ◽  
Spherical Shape ◽  
Pollutant Removal ◽  
Diffraction Field ◽  
X Ray Diffraction ◽  
Transmission Electron

Monodisperse nanoparticles are materials that are not agglomerate. The good characteristic of these materials is the dispersity in water, so they can better react with target pollutants. Accordingly, in this work, the monodisperse magnetite nanoparticles with the superparamagnetic property were synthesized and characterized. The hydrothermal method with the iron compound and polymer as precursors was conducted. The magnetic nanoparticles were characterized by several techniques including X-ray diffraction, field emission scanning electron microscope, transmission electron microscope, and vibrating sample magnetometer. The saturation magnetization (Ms) value, the coercivity (Hc), and the retentivity (Mr) were measured to demonstrate the paramagnetic behavior of the monodisperse magnetite nanoparticles. The results showed that the Fe3O4 nanoparticle were obtained at 200 °C for 16 h. The particles are monodispersed with the size approximately in the range of 60 - 250 nm as confirmed by FE-SEM and TEM images. These are the single grain and had the spherical shape similar to a blackberry. The saturation magnetization of 17.287 emu/g and ratio of retentivity to saturation magnetization (Mr/Ms) characterized the squareness of the hysteresis loops was 0.03653. It can be indicated that the Fe3O4 nanoparticles had superparamagnetic behavior. This property of Fe3O4 nanoparticles can draw pollutants to absorb on the surface of these nanomaterials. Then adsorbed pollutants can be easily removed by separating the Fe3O4 materials from water. This technique can be applied further in water treatment and pollutant removal.

Single-Crystal Iron Nanowire Arrays

2007 ◽  
Vol 121-123 ◽  
pp. 17-20 ◽  
Author(s):  
Yue Ling Sun ◽  
Ying Dai ◽  
L.Q. Zhou ◽  
Wen Chen
Keyword(s):  
Electron Microscope ◽  
Single Crystal ◽  
Hysteresis Loops ◽  
Nanowire Arrays ◽  
X Ray Diffraction ◽  
Easy Magnetization ◽  
Transmission Electron ◽  
Iron Nanowires ◽  
Xrd Patterns ◽  
Different Diameters

Highly ordered single-crystal iron nanowire arrays with different diameters have been fabricated in anodic aluminum oxide (AAO) templates by DC electrodeposition method. The Scanning Electron Microscope (SEM) and Transmission Electron Microscope (TEM) show that the iron nanowires are highly uniform and exhibit a single crystal structure. The X-ray diffraction (XRD) patterns of iron nanowire arrays indicate that most of the iron nanowire arrays have the obvious preferred orientation along the [200] direction. From the hysteresis loops of the iron nanowires, it reveals that the easy magnetization axes of nanowire arrays are along the long axis. The sample with smaller diameter (d=35nm) has a high square ratio (up to 98%) and a high coercive filed (1265Oe) when the external magnetic field is applied along axis of the nanowires. When the diameter decreases, the square ratio and the coercive field increase due to the single-domain structure and the strong shape anisotropy in the smaller diameter nanowire arrays.

Synthesis of Anatase/Brookite Mixtured TiO2 Nanoparticles by a Chimie Douce Technique

2013 ◽  
Vol 734-737 ◽  
pp. 2528-2531
Author(s):  
Yu Mei Gong ◽  
Qing Liang ◽  
Jing Guo ◽  
Hong Zhang ◽  
Fu Cheng Guan
Keyword(s):  
Electron Microscope ◽  
Anatase Phase ◽  
Spherical Shape ◽  
Nitrogen Adsorption ◽  
X Ray Diffraction ◽  
Average Pore ◽  
Specific Pore Volume ◽  
Transmission Electron ◽  
Bet Method ◽  
Ft Ir

Anatase/brookite mixtured TiO2nanoparticles have been synthesized by using a two-step process through a chimie douce technique. The as-prepared powders were characterized by Fourier transform infrared (FT-IR) spectra, X-ray diffraction (XRD), transmission electron microscope (TEM), scanning electron microscope (SEM), and a nitrogen adsorption apparatus in multipoint Brunauer-Emmett-Teller (BET) method. The results indicated that the TiO2nanoparticles were composed of biphasial anatase/brookite mixtures, 38% anatase phase formed in quasi-spherical shape and 62% brookite phase formed in nanorod shape. The specific surface area, the average pore diameter, and the specific pore volume were 100.06 m2/g, 14.0 nm, and 0.561 cm3/g, respectively.

Synthesis and Characterization of Cobalt Nanoparticles Prepared by Arc Discharge Method Using an Ultrasonic Nebulizer

2018 ◽  
Vol 52 ◽  
pp. 88-101 ◽  
Author(s):  
Ahmed M. El-Khatib ◽  
Mohamed S. Badawi ◽  
Gamal D. Roston ◽  
Alaa M. Khalil ◽  
Ramy M. Moussa ◽  
...  
Keyword(s):  
Dielectric Constant ◽  
Electron Microscope ◽  
Ac Conductivity ◽  
Arc Discharge ◽  
Spherical Shape ◽  
X Ray Diffraction ◽  
Ultrasonic Nebulizer ◽  
Transmission Electron ◽  
Co Nanoparticles ◽  
Discharge Method

Magnetic cobalt nanostructured was synthesized by a two-stage method. First, a solution of cobalt precursor droplets was prepared by an ultrasonic nebulizer. Second, the arc discharge method between two electrodes in an inert gas at atmospheric pressure is used to obtain the nanostructured cobalt powder. The sample obtained was characterized by X-ray diffraction (XRD). Scanning electron microscope (SEM), High Resolution Transmission Electron Microscope (HR-TEM), UV-Vis Spectrophotometry, zeta potential (ZP) and vibrating sample magnetometer (VSM). The dielectric constant, and AC conductivity of the prepared sample was determined in the frequency range of 4 Hz to 8 MHz. The investigations showed that the Co nanoparticles prepared in this way have smaller and homogeneous nanoparticles with spherical shape morphology with good stability and unique magnetic properties as compared with the bulky one. The dielectric properties analysis shows an enhancement in the dielectric constant and the AC conductivity of the Co nanoparticles.

scholarly journals Synthesis of BaTiO3 Nanoparticles via Hydrothermal Method

2017 ◽  
Vol 268 ◽  
pp. 172-176 ◽  
Author(s):  
Nurul Norfarina Hasbullah ◽  
Oon Jew Lee ◽  
Josephine Liew Ying Chyi ◽  
Soo Kien Chen ◽  
Zainal Abidin Talib
Keyword(s):  
Electron Microscope ◽  
Hydrothermal Method ◽  
Transmission Electron Microscope ◽  
Hydrothermal Process ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Average Size ◽  
Tga And Dsc

In this work, BaTiO3 nanoparticles were synthesized through hydrothermal method. The powder obtained from the hydrothermal process (as-synthesized powder) was calcined at 1000 °C. The phase formation and morphology of the as-synthesized and calcined powders were studied using X-ray diffraction (XRD), thermogravimetric (TGA) and differential scanning calorimetry (DSC) analyzer, and transmission electron microscope (TEM). The XRD data showed that the as-synthesized powder is partially amorphous. Upon calcining the powder at 1000 °C, highly crystalline BaTiO3 with tetragonal structure was obtained. As shown by TGA and DSC analysis, the precursor powder was completely transformed into BaTiO3 at 1000 °C. The presence of BaCO3 as an impurity phase in the powder is due to the lack of Ba2+ / Ti3+/4+. Transmission electron microscope images showed that the particle size of the as-synthesized powder increased after calcination due to crystal growth. In addition, nanocubes with the average size of around 11.66 nm were obtained as a result of the calcination compared to the ellipsoid like particles of the as-synthesized powder.

scholarly journals Synthesis, structure and magnetic properties of Y3Fe5-xAlxO12 garnets prepared by the soft chemical method

2014 ◽  
Vol 8 (4) ◽  
pp. 211-218 ◽  
Author(s):  
Pedro Ortega ◽  
Miguel Ramirez ◽  
César Foschini ◽  
Filiberto Garcia ◽  
Mario Cilense ◽  
...  
Keyword(s):  
Magnetic Properties ◽  
Saturation Magnetization ◽  
Single Phase ◽  
Hysteresis Loops ◽  
Stoichiometric Ratio ◽  
X Ray Diffraction ◽  
Spin Effects ◽  
Transmission Electron ◽  
Surface Spin ◽  
Iron Garnet

A study was undertaken about the structural, morphological and magnetic properties at room temperature of crystalline aluminium substituted yttrium iron garnet, YIG (Y3Fe5-xAlxO12 with 1.5< x < 1.7) nanoparticles prepared by polymeric precursormethod at the temperature of 700?C for 2 hours. The single-phase character and the well-defined structure of YIG nanoparticles were confirmed by X-ray diffraction, excluding the presence of any other phases. The Raman spectra showed that the changes of lattice vibration would influence interaction between the Fe ion and the host. Mean crystallite size of the single-phase powder was about 46-65 nm. Particles? morphology was investigated by high-resolution transmission electron microscopy, which shows that the particles were agglomerated. From hysteresis loops, particles? efficiency range from 91.4% to 95.9% as Fe/Al ratio decreases. Saturation magnetization was affected by the particle size and Fe/Al stoichiometric ratio. We observe that the saturation magnetization increases as the Fe/Al ratio is raised due to enhancement of the surface spin effects.

Strong Ultra-Violet Absorption in Cu Doped CeO2 Nanospheres

2018 ◽  
Vol 24 (8) ◽  
pp. 5947-5952 ◽  
Author(s):  
M Ponnar ◽  
K Pushpanathan
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Cerium Oxide ◽  
Field Emission ◽  
Diffraction Field ◽  
X Ray Diffraction ◽  
X Ray ◽  
Copper Doping ◽  
Transmission Electron ◽  
Scanning Electron

This article focuses the synthesis and characterization of copper doped cerium oxide nanospheres synthesized by chemical precipitation method. Synthesized nanopowders were characterized by means of X-ray diffraction, field emission scanning electron microscopy, transmission electron microscopy, ultraviolet-visible spectrometer and photoluminescence spectrometer. X-ray diffraction study confirmed the copper doping without disturbing the face centred cubic structure of cerium oxide. Field emission scanning electron microscope and transmission electron microscope study also confirmed the existence of sphere like nanoparticles. The optical absorption spectrum shows that the synthesized samples exhibit strong absorption in ultraviolet region and also it confirmed the decrease in energy gap of cerium oxide on copper doping. The photoluminescence study revealed that the blue emission is attributed to the fast oxygen transportation of copper doped cerium oxide nanoparticles.

Luminescent Properties of Gd2MoO6:Eu3+ Nanophosphor for WLEDs

2021 ◽  
Author(s):  
Yan Chen ◽  
Yuemei Lan ◽  
Dong Wang ◽  
Guoxing Zhang ◽  
Wenlong Peng ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Transmission Electron Microscope ◽  
Fluorescence Spectra ◽  
Solvothermal Method ◽  
Luminescent Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron

A series of Gd2-xMoO6:xEu3+(x=0.18-0.38) nanophosphors were synthesized by the solvothermal method. The properties of this nanophosphor were characterized by x-ray diffraction (XRD), transmission electron microscope (TEM), fluorescence spectra and diffuse...

scholarly journals Microscopic study of zinc nanoparticles synthesised using thermosetting polymer

2019 ◽  
Vol 49 (1) ◽  
Author(s):  
Giriraj Tailor ◽  
Jyoti Chaudhay ◽  
Deepshikha Verma ◽  
Bhupendra Kr. Sarma
Keyword(s):  
Electron Microscope ◽  
Xrd Analysis ◽  
The Novel ◽  
X Ray Diffraction ◽  
Zinc Nanoparticles ◽  
Transmission Electron ◽  
Sem Study ◽  
Zinc Salts ◽  
Thermosetting Polymer ◽  
Low Crystalline

AbstractThe present study reports the novel synthesis of Zinc nanoparticles (Zn NPs) by thermal decomposition method and its characterisation by Scanning Electron Microscope (SEM), Transmission Electron Microscope (TEM), and X-ray Diffraction Measurements (XRD). Synthesis of Zn NPs was achieved by using thermosetting polymer and zinc salts as precursor. Zn NPs were obtained on calcination at 850 °C for 30 min. SEM study reveals that synthesized nanoparticles are spherical in shape. XRD analysis shows that the Zn NPs formed are low crystalline in nature.

Formation of Graphite Encapsulated Nickel Nanoparticles by Ball Milling and Annealing of Expanded Graphite with Nickel

2011 ◽  
Vol 80-81 ◽  
pp. 217-220 ◽  
Author(s):  
Xue Qing Yue ◽  
Hai Jun Fu ◽  
Da Jun Li
Keyword(s):  
Electron Microscope ◽  
Ball Milling ◽  
Transmission Electron Microscope ◽  
Nickel Nanoparticles ◽  
Size Range ◽  
Expanded Graphite ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nickel Powders ◽  
Transmission Electron

Graphite encapsulated nickel nanoparticles were prepared by ball milling andsubsequently annealing a mixture of expanded graphite with nickel powders. The products were characterized by transmission electron microscope and X-ray diffraction. The formation mechanism of the products was discussed. Results show that the products have a size range of 20-150 nm. The graphite and nickel in the products all exhibit a high crystallinity.

Organoclay-reinforced polyethersulfone-modified epoxy-based hybrid nanocomposites

2011 ◽  
Vol 23 (7) ◽  
pp. 526-534 ◽  
Author(s):  
Yang Wang ◽  
Boming Zhang ◽  
Jinrui Ye
Keyword(s):  
Electron Microscopy ◽  
Fracture Toughness ◽  
Electron Microscope ◽  
Optical Microscope ◽  
Mechanical Analysis ◽  
Hybrid Nanocomposites ◽  
X Ray Diffraction ◽  
Transmission Electron ◽  
Modified Epoxy ◽  
Scanning Electron

Hybrid nanocomposites were successfully prepared by the incorporation of polyethersulfone (PES) and organoclay into epoxy resin. They had higher fracture toughness than the prepared PES/epoxy blend and organoclay/epoxy nanocomposites. The microstructures of the hybrid nanocomposites were studied. They were comprised of homogeneous PES/epoxy semi-interpenetrating network (semi-IPN) matrices and organoclay micro-agglomerates made up of tactoid-like regions composed of ordered exfoliated organoclay with various orientations. The former was confirmed with dynamic mechanical analysis, scanning electron microscopy and transmission electron microscopy, while the latter was successfully observed with X-ray diffraction measurements, optical microscope, scanning electron microscope and transmission electron microscope. The improvement of their fracture toughness was due to the synergistic toughening effect of the PES and the organoclay and related to their microstructures.

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