scholarly journals A Comparison between Chemical Synthesis Magnetite Nanoparticles and Biosynthesis Magnetite

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Seyed Abolghasem Kahani ◽  
Zahra Yagini

The preparation of Fe3O4from ferrous salt by air in alkaline aqueous solution at various temperatures was proposed. The synthetic magnetites have different particle size distributions. We studied the properties of the magnetite prepared by chemical methods compared with magnetotactic bacterial nanoparticles. The results show that crystallite size, morphology, and particle size distribution of chemically prepared magnetite at 293 K are similar to biosynthesis of magnetite. The new preparation of Fe3O4helps to explain the mechanism of formation of magnetosomes in magnetotactic bacteria. The products are characterized by X-ray powder diffraction (XRD), infrared (IR) spectra, vibrating sample magnetometry (VSM), and scanning electron microscopy (SEM).

1989 ◽  
Vol 178 ◽  
Author(s):  
Carol L. Kilgour ◽  
Kenneth L Bergeson ◽  
Scott Schlorholtz

AbstractFly ashes from the Lansing and Ottumwa power plants in Iowa were agglomerated by means of a continuous pan agglomerator, a continuous auger and a batch turbine agglomerator. In order to compare agglomeration mechanisms the following parameters were determined: (a) particle size distributions of the untreated fly ashes; (b) particle size distributions of the agglomerated fly ashes; (c) pore size distribution of agglomerates; (d) crystalline hydration products by X-ray diffraction; and (e) morphological characterization by scanning electron microscopy.In the batch system coalescence mechanisms were favoured. The agglomerates were fairly irregular in shape and had a rough surface texture. As residence time in the system increased breakage of agglomerates occurred, reducing the average agglomerate size. In the continuous systems layering of the fine feed particles onto established agglomerates was the predominant growth mechanism. The agglomerates were smooth and spherical. The layer structure was observed by scanning electron microscopy. Agglomerates of widely varying size, strength, and pore matrix can be produced in both systems. It is envisaged that while agglomerates could be produced with characteristics essential for their proposed end use by either method, continuous pan agglomeration would be the most versatile system to utilize.


1991 ◽  
Vol 245 ◽  
Author(s):  
Carol L. Kilgour

ABSTRACTFluidized bed combustion (FBC) residues from four Iowa power plants were characterized to provide background with respect to chemical, physical, mineralogical and microstructural parameters that might affect their utilization potential. Methodologies used include: bulk chemical analysis; grain size analysis; specific gravity determination; mineralogical analysis by x-ray diffraction; scanning electron microscopy; and thermal analysis.Chemical analysis of the major components showed the separation of the constituents during combustion. The bottom ash is derived from the calcined and partly sulfated limestone, thus the concentration of calcium and sulfur compounds is greater. The fly ash however is derived mostly from the coal and therefore exhibits higher concentrations of coal ash components such as silica (SiO2), alumina (Al2O3), and ferric oxide (Fe2O3). The alkalis appear to be more concentrated in the fly ash.The measured particle size distributions of the bulk samples varied greatly, from extremely coarse (mean particle size ˜2000 μm) to fine (mean particle size ˜25 μm). The size distributions also varied in breadth. Specific gravities values recorded ranged from about 2.65 to about 3.05.X-ray diffraction analyses showed that most of the FBC by-products contain, as easily detectable crystalline components, only quartz, anhydrite and lime, and as is to be expected due to the low combustion temperatures, do not show broad peaks characteristic of glass in conventional fly ashes. Scanning electron microscopy revealed the FBC by-products to be extremely intricate mixtures of particles of complex and variable composition and internal structure.FBC by-products are shown to be extremely complex mixtures of particles of variable composition and internal structure. However, despite their local variation, useful results can be obtained by overall chemical and physico-chemical analyses of their composition. The exploitable properties of FBC residue include the somewhat cementitious nature and the granularity. However, their heterogeneous nature, lack of pozzolanic properties, and elevated sulfate content may limit their uses, especially in construction.


2012 ◽  
Vol 554-556 ◽  
pp. 709-713
Author(s):  
Yan Hong Liu ◽  
Hong Wen Ma ◽  
Mei Tang Liu

The morphology and particle size of boehmite play a decisive role on the application of alumina that derived from it. In this paper, we employed pseudoboehmite that produced from Al2 (SO4)3•18H2O and NH3•H2O at 70 °C, pH 7.5 as precursor to synthesize boehmite, and utilized different seeding when preparing pseudoboehmite and boehmite. To identify the influence of seeding on the microstructure of pseudoboehmite and boehmite, the products were characterized by X-ray powder diffraction (XRD), field-emission scanning electron microscopy (FE-SEM) and BET. The results indicate that the pseudoboehmite seeding has a significant influence on the morphology and particle size of pseudoboehmite to which we should pay high attention. However, the boehmite seeding does not play the role of crystal nucleus as expected. The further intrinsic mechanism study is ongoing.


MRS Advances ◽  
2020 ◽  
Vol 5 (29-30) ◽  
pp. 1623-1623
Author(s):  
Adriana Valério ◽  
Sérgio L. Morelhão ◽  
Alex J. Freitas Cabral ◽  
Márcio M. Soares ◽  
Cláudio M. R. Remédios

2015 ◽  
Vol 1109 ◽  
pp. 314-318
Author(s):  
Nor Diyana Abdul Aziz ◽  
Kelimah Elong ◽  
Norlida Kamarulzaman

Tin Oxide (SnO2) is a metal oxide which has many applications in industry. In this study, SnO2 powders were synthesized by a self-propagating combustion (SPC) method. The product was annealed at 800 °C for 12 and 24 h before characterizing with X-Ray Diffraction (XRD) for phase studies. X-Ray Diffraction results showed that both samples are pure of tetragonal structure with space group P42/mnm. The sample annealed at a longer period, that is, 24 h, shows a higher degree of crystallinity compared to the 12 h annealed sample. It also shows a smaller full width at half maximum (FWHM), indicating larger crystallite size for the 24 h annealed sample. The particle size analysis reveals that there are two groups of particle size distributions for both samples. SEM results give values that are different from the particle sizer results due to the different nature of the measurement methods.


2010 ◽  
Vol 434-435 ◽  
pp. 850-852
Author(s):  
Qi Wang ◽  
Bo Yin ◽  
Zhen Wang ◽  
Gen Li Shen ◽  
Yun Fa Chen

In present work, ceria microspheres were synthesized by template hydrothermal method. Crystalline form of the as-synthesized ceria microspheres was defined by X-ray powder diffraction (XRD) and high resolution transmission electron microscopy (HRTEM). Dispersibility of ceria microspheres was comprehensively characterized using scanning electron microscope (SEM) observation and laser particle size analyzer. Furthermore, the ultraviolet light absorption performances of ceria microspheres with several different sizes were compared by ultraviolet visible spectrophotometer. The results showed that ceria microspheres presented excellent UV absorbent property and the size influence was remarkable.


2016 ◽  
Vol 680 ◽  
pp. 257-260
Author(s):  
Meng Yun Dong ◽  
Cheng Zhang ◽  
Jin Feng Xia ◽  
Hong Qiang Nian ◽  
Dan Yu Jiang

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.


2010 ◽  
Vol 03 (03) ◽  
pp. 185-188 ◽  
Author(s):  
XIAOYUN ZHAN ◽  
ZHAOHUI LI ◽  
JIAOJUN TANG ◽  
QIZHEN XIAO ◽  
GANGTIE LEI ◽  
...  

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.


2010 ◽  
Vol 03 (02) ◽  
pp. 125-129 ◽  
Author(s):  
CAIQUAN ZHANG ◽  
YALI CUI ◽  
DIDI ◽  
KUNPING YAN ◽  
CHAO CHEN ◽  
...  

Facile procedures to synthesize large quantities of uniform and well dispersed magnetite particles in water were developed through a solvothermal method. Magnetite microspheres were obtained by using FeCl 3 · 6H 2 O , urea and polyethylene glycol as the starting materials in ethylene glycol at 200°C for 8 h. The samples were characterized by using X-ray diffraction, transmission electron microscopy, scanning electron microscopy and vibrating sample magnetometry. Experimental results revealed that the particles were well dispersed with uniform particle size and diameters in the range 260 to 280 nm. The saturation magnetization value was 71.5 emu/g with negligible remanence.


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