Preparation of Hollow Nickel Ferrite Microspheres and their Magnetic Properties

2014 ◽  
Vol 1035 ◽  
pp. 488-491
Author(s):  
Jing Jing Li ◽  
Yun Zhao ◽  
Han Sheng Li ◽  
Qin Wu ◽  
Qing Ze Jiao
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Nickel Ferrite ◽  
Room Temperature ◽  
Solvothermal Method ◽  
Magnetization Measurement ◽  
Vibrating Sample Magnetometer ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

Hollow nickel ferrite microspheres with a diameter of about 1.5 to 2.5 μm were synthesized using an emulsion-based solvothermal method in combination with calcination at 550°C. The structures and morphologies of the nickel ferrite microspheres were characterized using an X-ray diffractometer, a transmission electron microscopy and a field emission scanning electron microscopy. Magnetization measurement was carried out using a vibrating sample magnetometer at room temperature. The saturation magnetization and coercivity of nickel ferrite microspheres could reach 19.41 emu/g and 202.28 Oe, respectively. Hollow nickel ferrite microspheres might be used as catalysts, magnetic materials and microwave absorbers.

Synthesis of Silicon Carbide Nanoparticles from Carbon Nanotubes

2012 ◽  
Vol 602-604 ◽  
pp. 183-186 ◽  
Author(s):  
Jing Liu ◽  
Rong Wu ◽  
Jin Li ◽  
Yan Fei Sun ◽  
Ji Kang Jian
Keyword(s):  
Electron Microscopy ◽  
Carbon Nanotubes ◽  
Scanning Electron Microscopy ◽  
Silicon Carbide ◽  
Room Temperature ◽  
Sic Nanoparticles ◽  
X Ray ◽  
Transmission Electron ◽  
Cubic Silicon Carbide ◽  
Scanning Electron

In this paper, we report the synthesis of cubic silicon carbide (3C-SiC) nanoparticles by direction reaction of silicon powders and carbon nanotubes. The as-prepared SiC nanoparticles were characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscopy and Raman scattering at room temperature. The possible growth mechanism is proposed.

scholarly journals Fabrication and magnetic properties of hierarchical nickel microwires with nanothorns

2010 ◽  
Vol 8 (2) ◽  
pp. 434-439 ◽  
Author(s):  
Junhao Zhang ◽  
Ling Yang ◽  
Xiaofang Cheng ◽  
Jinmeng Zhang ◽  
Fucai Li
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Magnetic Properties ◽  
Room Temperature ◽  
Cooperative Effect ◽  
Magnetic Interactions ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

AbstractHierarchical nickel microwires with nanothorns were fabricated through a reduction of nickelous salt with hydrazine in diethanolamine. The product was characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), and energy-dispersive X-ray spectroscopy (EDS). The growth mechanism of the nickel microwires with nanothorns is proposed, based on the evolution of the structures and morphologies, which could be ascribed to the cooperative effect of the complexant of diethanolamine and inherent magnetic interactions. Magnetic properties of the product were measured at room temperature and compared with other shaped counterparts.

Synthesis of NaFeS2 Nanorods by Solvothermal Technique

2013 ◽  
Vol 774-776 ◽  
pp. 603-608 ◽  
Author(s):  
Feng Huang ◽  
Rong Wu ◽  
Jin Li ◽  
Yan Fei Sun ◽  
Ji Kang Jian
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Magnetic Property ◽  
Electron Microscope ◽  
Powder Diffraction ◽  
Vibrating Sample Magnetometer ◽  
X Ray ◽  
Solvothermal Technique ◽  
Transmission Electron ◽  
Scanning Electron

Ternary NaFeS2nanorods were synthesized by solvothermal technique from Fe2O3and Na2S2O3·H2O in ethylenediamine (en) solvent. The phase, morphology, microstructure and magnetic property of the nanorods were characterized by X-ray powder diffraction, scanning electron microscopy, transmission electron microscope and vibrating sample magnetometer. The possible growth mechanism of NaFeS2nanorods was discussed.

scholarly journals Exploring Structural, Morphological, and Magnetic Properties of Zinc Nickel Ferrites Systems Nanocomposites

2020 ◽  
Vol 11 (1) ◽  
pp. 7785-7793
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Nickel Ferrite ◽  
Room Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Co Precipitation ◽  
Ferrite System ◽  
Zinc Nickel ◽  
Scanning Electron

The formation of Zinc Nickel Ferrites Systems Nanocomposites (ZNFONCs) through Ethylene glycol (PEG) surfactant was achieved by chemical co-precipitation technique. Their structure, shape, and constituents were investigated by X-ray diffraction, dispersion, and scanning electron microscopy. The photocatalyst effect of Zinc-Nickel ferrite system Nanocomposites was determined by methyl Blue (MB), when exposed to ultraviolet light. Magnetization estimation by vibrating magnetometer at room temperature is an additional effort in the present work.

Identification of calcium oxalate crystals in dried or fixed tobacco leaf

1984 ◽  
Vol 42 ◽  
pp. 288-289
Author(s):  
Vicki L. Baliga ◽  
Mary Ellen Counts
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Calcium Oxalate ◽  
Growth And Development ◽  
Polarized Light ◽  
Calcium Oxalate Crystals ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

Calcium is an important element in the growth and development of plants and one form of calcium is calcium oxalate. Calcium oxalate has been found in leaf seed, stem material plant tissue culture, fungi and lichen using one or more of the following methods—polarized light microscopy (PLM), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and x-ray diffraction.Two methods are presented here for qualitatively estimating calcium oxalate in dried or fixed tobacco (Nicotiana) leaf from different stalk positions using PLM. SEM, coupled with energy dispersive x-ray spectrometry (EDS), and powder x-ray diffraction were used to verify that the crystals observed in the dried leaf with PLM were calcium oxalate.

Hydrothermal Synthesis and Characterization of BiFeO3 Polyhedral Crystallites

2012 ◽  
Vol 174-177 ◽  
pp. 508-511
Author(s):  
Lin Lin Yang ◽  
Yong Gang Wang ◽  
Yu Jiang Wang ◽  
Xiao Feng Wang
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Xrd Pattern ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

BiFeO3 polyhedrons had been successfully synthesized via a hydrothermal method. The as-prepared products were characterized by power X-ray diffraction (XRD) pattern, scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The possible mechanisms for the formation of BiFeO3 polyhedrons were discussed. Though comparison experiments, it was found that the kind of precursor played a key role on the morphology control of BiFeO3 crystals.

Identification of Nd163 phase in melt-textured NdBa2Cu3O7−δ bulk samples

2003 ◽  
Vol 18 (9) ◽  
pp. 2050-2054 ◽  
Author(s):  
Marcello Gombos ◽  
Vicente Gomis ◽  
Anna Esther Carrillo ◽  
Antonio Vecchione ◽  
Sandro Pace ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Optical Microscopy ◽  
Room Temperature ◽  
Polarized Light ◽  
Energy Dispersive ◽  
X Ray ◽  
Spontaneous Formation ◽  
The Stability ◽  
Scanning Electron

In this work, we report on the observation of Nd1Ba6Cu3O10,5 (Nd163) phase of the NdBaCuO system in melt-textured Nd123 bulk samples grown from a mixture of Nd123 and Nd210 phase powders. The observation was performed with polarized light optical microscopy and scanning electron microscopy–energy dispersive x-ray analyses. Images of the identified phase crystals show an aspect quite different from Nd422 crystals. Unexpectedly, Nd163 was individuated, even in “pure” Nd123 samples. Moreover, after long exposure to air, Nd163 disappeared completely in samples synthesized from powders containing Nd210. Thermogravimetry analyses of powders show that the stability of this phase in air is limited to temperatures higher than 900 °C, so Nd163 is unstable and highly reactive at room temperature. Moreover, an explanation of the observation of Nd163 in Nd210 free samples, based on the spontaneous formation of Nd163 phase in a Nd123 melt, is proposed.

Influence of Salt Aid on Combustion Synthesis of Nanocrystalline CeO2 Powders

2011 ◽  
Vol 412 ◽  
pp. 5-8 ◽  
Author(s):  
Ying Zhang ◽  
Ai Chen ◽  
Hai Rong Wang ◽  
Ze Song Li ◽  
Ying Ping Shen
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Combustion Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Particle Characteristics ◽  
Transmission Electron ◽  
Nanocrystalline Ceria ◽  
Scanning Electron

The present article reports the results of studies related to the synthesis of nanocrystalline ceria powder by combustion process using salt combustion aid. Cerium nitrate as oxidant and urea as fuel were used as reagents, Sodium Chloride was compared as combustion aid. The phase analysis and particle size were compared. The product was characterized by X-ray diffraction, Scanning electron microscopy and Transmission electron microscopy. The results showed that employment of starting fuel with combustion aid resulted in synthesizing nanocrystalline ceria powder with fine agglomerates. By using combustion aid, the energetics of the combustion reaction and particle characteristics have been changed.

A Facile Fynthesis of ZnS Nanostructures via Liquid-Solid Reactions

2014 ◽  
Vol 979 ◽  
pp. 184-187
Author(s):  
Weerachon Phoohinkong ◽  
Thitinat Sukonket ◽  
Udomsak Kitthawee
Keyword(s):  
Electron Microscopy ◽  
Room Temperature ◽  
Inorganic Salts ◽  
Chloride Salt ◽  
X Ray ◽  
Commercial Grade ◽  
Transmission Electron ◽  
Salt Addition ◽  
20 Nm ◽  
Scanning Electron

Zinc sulfide (ZnS) nanostructures are important materials for many technologies such as sensors, infrared windows, transistors, LED displays, and solar cells. However, many methods of synthesizing ZnS nanostructures are complex and require expensive equipment. In this study, a liquid-solid chemical reaction without surfactant was used to synthesize ZnS at room temperature. In addition, commercial grade zinc oxide (ZnO) particles were used as a precursor. The effect of the addition of acids and inorganic salts were investigated. The products were characterized by field emission scanning electron microscopy (FESEM) coupled with energy-dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM). The results show that the nanoparticles of ZnS were obtained in hydrochloric acid and acetic acid addition. The diameters were in the range of 10 to 20 nm and 50 to 100 nm, respectively. In the case of a sodium chloride salt addition, a ZnS structure was obtained with a particle size of approximately 5 nm and a flake-like morphology.

N-type Ba0.2Co4Sb11.5Te0.5: Optimization of thermoelectric properties by different pressures

2019 ◽  
Vol 33 (03) ◽  
pp. 1950027 ◽  
Author(s):  
Jiaxiang Chen ◽  
Xiaopeng Jia ◽  
Yuewen Zhang ◽  
Haiqiang Liu ◽  
Baomin Liu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Seebeck Coefficient ◽  
Room Temperature ◽  
X Ray Diffraction ◽  
Absolute Value ◽  
X Ray ◽  
Coefficient Increase ◽  
Maximum Power Factor ◽  
Scanning Electron

The polycrystalline skutterudite [Formula: see text] were successfully synthesized from 1.5 GPa to 3.5 GPa by the high pressure and high temperature (HPHT) method. Negative Seebeck coefficient confirmed the n-type conductivity of all samples. The phase compositions of samples were investigated by X-ray diffraction (XRD) and the microstructures were observed by scanning electron microscopy (SEM). It was found that the grains appeared smaller and the grain boundaries became more abundant when pressures were higher. We measured the electrical properties from room temperature to 723 K. Both the electrical resistivity and absolute value of Seebeck coefficient increase with the increasing synthetic pressure. At 723 K, the maximum power factor of [Formula: see text] was obtained for the sample synthesized under 3 GPa. The maximum ZT value of 0.61 was reached by [Formula: see text] synthesized under 3 GPa and measured at 723 K.

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