Synthesis and characterization of high-energy ball milled nanostructured Fe50Ni50
Identifieur interne : 000202 ( France/Analysis ); précédent : 000201; suivant : 000203Synthesis and characterization of high-energy ball milled nanostructured Fe50Ni50
Auteurs : A. Djekoun [Algérie] ; A. Otmani [Algérie] ; B. Bouzabata [Algérie] ; L. Bechiri [Algérie] ; N. Randrianantoandro [France] ; J. M. Greneche [France]Source :
- Catalysis today [ 0920-5861 ] ; 2006.
Descripteurs français
- Pascal (Inist)
English descriptors
- KwdEn :
Abstract
Mechanical alloying is a non-equilibrium process for materials synthesis. It has been used to obtain nanocrystalline binary system FeNi. Fe and Ni elemental powders have been ball milled in a planetary mill (Pulverisette 7, Fritsch) for various times up to several hours. The morphology of the powders was examined using scanning electron microscopy (SEM). X-ray diffraction (XRD) has been employed to follow the structural evolution during the ball milling process. The X-ray patterns were analysed by the MAUD procedure, which is based on the Rietveld method combined with a Fourier analysis, well adapted for broadened diffraction peaks. The grain size was found to be about 5 nm and the residual strain was about 0.021% after 322 h of milling. The as-milled samples, characterized by Mössbauer spectroscopy (MS) contain a mixture of a (bcc) and γ (fcc) phases after 48 h of ball milling.
Affiliations:
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Pascal:06-0371433Le document en format XML
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<term>Iron Oxides</term>
<term>Mechanical alloying</term>
<term>Moessbauer spectrometry</term>
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<term>Nickel Oxides</term>
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<term>Caractérisation</term>
<term>Energie</term>
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<term>Alliage mécanique</term>
<term>Spectrométrie Mössbauer</term>
<term>Catalyse hétérogène</term>
<term>Fer Oxyde</term>
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<front><div type="abstract" xml:lang="en">Mechanical alloying is a non-equilibrium process for materials synthesis. It has been used to obtain nanocrystalline binary system FeNi. Fe and Ni elemental powders have been ball milled in a planetary mill (Pulverisette 7, Fritsch) for various times up to several hours. The morphology of the powders was examined using scanning electron microscopy (SEM). X-ray diffraction (XRD) has been employed to follow the structural evolution during the ball milling process. The X-ray patterns were analysed by the MAUD procedure, which is based on the Rietveld method combined with a Fourier analysis, well adapted for broadened diffraction peaks. The grain size was found to be about 5 nm and the residual strain was about 0.021% after 322 h of milling. The as-milled samples, characterized by Mössbauer spectroscopy (MS) contain a mixture of a (bcc) and γ (fcc) phases after 48 h of ball milling.</div>
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