Effects of Mechanical Alloying on the Structure and Properties of Iron Powders

2015 ◽  
Vol 364 ◽  
pp. 132-138
Author(s):  
F. Lemdani ◽  
Mohammed Azzaz ◽  
K. Taïbi ◽  
A. Lounis

A nanostructured iron, elaborated from pure elemental powders by mechanical milling at high energy was characterized by different types of technical of analysis. Scanning electron microscopes (SEM) and laser scattering machine have showed the variation in the size and the shape of particles according to different milling times. Powders obtained were characterized with X-ray diffraction (XRD) , the latter diffraction patterns indicated the body centered cubic (bcc) structure. The crystalline grain was about 13 nm size after only a few hours of milling time. The measurement of both coercive field (Hc) and maximal magnetization (Ms) revealed a change in the magnetic behavior of our samples.

2013 ◽  
Vol 26 ◽  
pp. 75-81 ◽  
Author(s):  
S. Triaa ◽  
L. Faghi ◽  
F. Kali-Ali ◽  
M. Azzaz

Nanostructured iron based alloy, elaborated from pure elemental powders by mechanical milling at high energy was studied. The materials obtained were characterized by several techniques, such as X-ray diffraction (XRD), which allowed the dissolution of chromium in the iron phase as a function of milling time. The peaks indicate that the obtained solid solution has the body centred cubic (bcc) structure, for a speed of 250 rpm after 24 hours milling time. The Williamson - Hall analysis method was used to exploit the recorded XRD patterns. The crystallite size of about 14 nm and the microstrain of about 0.90% were obtained for 48 hours of milling. Scanning electron microscopes (SEM) and EDX analysis have confirmed the refining of milled particles as a function of milling time and the homogenization of our powders. The measurement of reflection coefficient has revealed an increase in the microwave absorption versus milling time and has confirmed the formation of our alloy during 24 hours of milling.


2010 ◽  
Vol 97-101 ◽  
pp. 3879-3883 ◽  
Author(s):  
Zhi Bo Yang ◽  
Jiu Hua Xu ◽  
Ai Ju Liu

Brazing diamond grits onto steel substrate using a Ni-based filler alloy was carried out via laser beam in an argon atmosphere. The microstructure of the interfacial region among the Diamond grits and the filler layer were investigated by means of scanning electron microscopes (SEM), X-ray diffraction (XRD) and energy dispersive X-ray spectroscopy (EDS). Meanwhile, the formation mechanism of carbide layers was discussed. All the results indicated that the active element chromium in the Ni-based alloy concentrated preferentially to the surface of the grits to form a chromium-rich layer, and the hard joint between the alloy and the steel substrate is established through a cross-diffusion of iron and Ni-based alloy through parameters optimization.


1998 ◽  
Vol 13 (5) ◽  
pp. 1171-1176 ◽  
Author(s):  
S-H. Yip ◽  
D. Guay ◽  
S. Jin ◽  
E. Ghali ◽  
A. Van Neste ◽  
...  

The structural and electrochemical properties of the Ti–Ru–Fe–O system have been studied over the whole ternary metal compositional range, keeping constant the oxygen content at 30 at.%. The phase diagram was explored systematically by varying the composition of the material along one of the following axes: (i) constant Ru content of 16 at. %; (ii) constant Ti/Ru ratio of 2; (iii) constant Ti/Fe ratio of 1.6. For O/Ti ratios equal or below unity, the most prominent peaks observed in the x-ray diffraction patterns belong to a B2 structure. For O/Ti ratio larger than unity, stable titanium oxide phases are formed, which coexist with a cubic Fe-like or hcp-Ru like phases depending on the Fe/Ru ratio. Powder compositions with stoichiometry close to Ti2RuFeO2 are of interest due to good electrocatalytic properties, long-term stability, and low Ru content.


Catalysts ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1161
Author(s):  
Tao Ji ◽  
Enna Ha ◽  
Mingzhou Wu ◽  
Xin Hu ◽  
Jie Wang ◽  
...  

Bi2MoO6 with a tunable morphology was synthesized by a facile hydrothermal route using different surfactants, including nanosheet-assembled microspheres, smooth microspheres, nanoparticle aggregates and nanoparticles. The morphology, crystal structure and photocatalytic activity of as-obtained Bi2MoO6 were characterized by scanning electron microscopes (SEM), X-ray diffraction (XRD), photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET) and UV–Vis spectrophotometer. Bi2MoO6 flower-like microspheres using cetyl-trimethyl-ammonium bromide (BET) as the surfactant exhibited much better photocatalytic activity than Bi2MoO6 with the other morphologies, with a degradation efficiency of 98.4%. It can be summarized that the photocatalytic activity of Bi2MoO6 samples depends on their morphology and composition.


1977 ◽  
Vol 86 (4) ◽  
pp. 525-540 ◽  
Author(s):  
David J. Lim ◽  
William H. Saunders

A total of 32 otosclerotic stapes is thin-sectioned without decalcification and examined using transmission and scanning electron microscopes, with a nondispersive x-ray analyzer attached to the latter. These otosclerotic stapes are classified as spongiotic, sclerotic, or preotosclerotic, according to their pathologic characteristics and state of mineralization. Either diffuse or patchy demineralization in the ground substance appears to be the initial stage of otosclerosis, and this area coincides with preotosclerotic lesions (also known as blue mantle) in light microscopy. Therefore, it is interpreted that demineralization precedes the destruction of ground substance in the preotosclerotic lesion. Bone mineral deposits in new otosclerotic bone appear to be related to the collagen fibrils that are embedded in the ground substance. No mineral deposit could be seen without the ground substance deposition; therefore, it is suggested that this ground substance is the single most important factor in the poor mineralization of the otosclerosis. The sclerotic lesions are well mineralized and show a typical pattern of hydroxyapatite by x-ray diffraction study. We could not confirm the notion that the sclerotic lesion is hypermineralized as compared to the normal stapes. The spongiotic lesions are poorly mineralized, with low calcium salt. Using the Ca/P ratio and x-ray diffraction pattern as criteria, it was determined that spongiotic lesions belong to unstable, immature bone.


2011 ◽  
Vol 672 ◽  
pp. 171-174
Author(s):  
Ionel Chicinaş ◽  
P. Cârlan ◽  
Florin Popa ◽  
Virgiliu Călin Prică ◽  
Lidia Adriana Sorcoi

The Ir-Al powder in the 1:1 atomic ratio was obtained by high energy mechanical alloying in a Pulverisette 4 Fritch planetary mill. The final product was obtained after 28 h of milling in argon atmosphere. Alloy formation was investigated by X-ray diffraction. After 4 h of milling the new structure of IrAl compound is found in the diffraction patterns. The obtained powders are nanocrystalline with a mean crystallite size of 11 nm after 28 h of milling. The particle morphology and the chemical homogeneity were studied using scanning electron microscopy (SEM) and energy dispersive spectrometry (EDX). It was found that the obtained compound present large particles composed by smaller one.


2012 ◽  
Vol 1396 ◽  
Author(s):  
Mohana K. Rajpalke ◽  
Thirumaleshwara N. Bhat ◽  
Basanta Roul ◽  
Mahesh Kumar ◽  
S. B. Krupanidhi

ABSTRACTNonpolar a-plane InN/GaN heterostructures were grown by plasma assisted molecular beam epitaxy. The growth of nonpolar a- plane InN / GaN heterostructures were confirmed by high resolution x-ray diffraction study. Reflection high energy electron diffraction patterns show the reasonably smooth surface of a-plane GaN and island-like growth for nonpolar a-plane InN film, which is further confirmed by scanning electron micrographs. An absorption edge in the optical spectra has the energy of 0.74 eV, showing blueshifts from the fundamental band gap of 0.7 eV. The rectifying behavior of the I-V curve indicates the existence of Schottky barrier at the InN and GaN interface. The Schottky barrier height (φb) and the ideality factor (η) for the InN/GaN heterostructures found to be 0.58 eV and 2.05 respectively.


1992 ◽  
Vol 263 ◽  
Author(s):  
R.J. Matyi ◽  
H.J. Gillespie ◽  
G.E. Crook ◽  
J.K. Wade

ABSTRACTThe growth of high quality Si/GaAs superlattices on GaAs substrates using molecular beam epitaxy is described. A typical superlattice structure consisted of ten periods of thin (<5Å) layers of pseudomorphic silicon alternating with thick GaAs layers; typical GaAs thicknesses range from 100Å to 1850Å. In situ reflection high energy electron diffraction analysis of the structures during growth showed the silicon layers developed a (3 ×1) reconstruction, while the GaAs exhibited a (4×2)→(3×2)→(3×1)→(2×4) reconstruction sequence. Both observations agree with prior studies of the growth of embedded silicon in GaAs/Si/GaAs heterostructures. X-ray diffraction using the (004) reflection showed sharp and intense satellite peaks (out to 22 orders in one case), indicating a high level of structural quality. Very good agreement has been obtained between observed diffraction patterns and those calculated via dynamical simulation.


1970 ◽  
Vol 24 (6) ◽  
pp. 557-566 ◽  
Author(s):  
R. S. Frankel ◽  
D. W. Aitken

A review is given of recent developments in energy-dispersive x-ray emission spectroscopy, with the aim of providing both an introductory and usefully practical look at this innovative field. The review begins with the first principles of x-ray production and observation, including a brief comparison of the performance capabilities of different types of detectors, but then specializes to a major extent in solid state x-ray spectrometers, which have led to the most significant new developments and applications. Evidence is presented which suggests that we are nearing an asymptotic limit in the attainment of ever better resolution with these types of systems. Applications that have been made possible by significant improvements in system resolution are discussed, but in the context of the need for a realistic appraisal of over-all system requirements. The great advantages offered by the marriage of silicon x-ray spectrometers to scanning electron microscopes and electron microprobe analyzers are reviewed and illustrated.


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