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Fe-Co-B amorphous alloy powder by chemical reduction

Corrias, A., Ennas, G., Licheri, G., Marongiu, G., Musinu, A., Paschina, G., Piccaluga, G., Pinna, G. (1988) Fe-Co-B amorphous alloy powder by chemical reduction. Journal of Materials Science Letters, 7 (4). pp. 407-409. ISSN 0261-8028. (doi:10.1007/BF01730759) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided) (KAR id:46253)

The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided.
Official URL:
http://dx.doi.org/10.1007/BF01730759

Abstract

Fine boride powders, prepared by reactions between sodium or potassium borohydride and aqueous (or alcoholic) solutions of transition metal salts have long been known to be good catalysts for hydrogenation reactions. New interest around them has recently grown, because they were found to exhibit amorphous structure. Classical chemical reactions may thus offer a simple route to prepare amorphous metal powders, paralleling more sophisticated methods so far used to reach the same goal. To explore the potential of these reactions, we considered the system Fe-Co-B with the aim of examining the characteristics of the product obtained in the easiest way and without any particular precautions. The structure of the amorphous alloy appears to be different from that of materials with a similar Me/B ratio prepared via melt spinning.

Item Type: Article
DOI/Identification number: 10.1007/BF01730759
Uncontrolled keywords: BORON COMPOUNDS - Reduction, GLASS, METALLIC - Structure, POWDER METAL PRODUCTS - Manufacture, AMORPHOUS METAL POWDERS, BORIDE POWDERS, CHEMICAL REDUCTION, POTASSIUM BOROHYDRIDE, IRON COBALT BORON ALLOYS
Subjects: Q Science > QC Physics > QC176.8.N35 Nanoscience, nanotechnology
Divisions: Divisions > Division of Natural Sciences > Physics and Astronomy
Depositing User: Anna Corrias
Date Deposited: 17 Dec 2014 12:11 UTC
Last Modified: 05 Nov 2024 10:29 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/46253 (The current URI for this page, for reference purposes)

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