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dc.contributor.authorSreekumar, V M-
dc.contributor.authorPillai, R M-
dc.contributor.authorPai, B C-
dc.contributor.authorChakraborty, M-
dc.date.accessioned2015-01-16T07:43:03Z-
dc.date.available2015-01-16T07:43:03Z-
dc.date.issued2008-
dc.identifier.citationScience and Technology of Advanced Materials 9(1):Article No. 015004;Jan-Mar 2008en_US
dc.identifier.issn1468-6996-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1767-
dc.description.abstractAl/MgAl2O4 in situ metal matrix composites have been synthesized using value-added silica sources (microsilica and rice husk ash) containing similar to 97% SiO2 in Al-5 wt.% Mg alloy. The thermodynamics and kinetics of MgAl2O4 formation are discussed in detail. The MgO and MgAl2O4 phases were found to dominate in microsilica (MS) and rice husk ash (RHA) value-added composites, respectively, during the initial stage of holding the composites at 750 degrees C. A transition phase between MgO and MgAl2O4 was detected by the scanning electron microscopy and energy-dispersive spectroscopy (SEM-EDS) analysis of the particles extracted from the composite using 25% NaOH solution. This confirms that MgO is gradually transformed to MgAl2O4 by the reaction 3SiO(2(s)) + 2MgO((s)) + 4Al((1)) -> 2MgAl(2)O(4(s)) + 3Si((1)). The stoichiometry of MgAl2O4, n, computed by a new methodology is between 0.79 and 1.18. The reaction between the silica sources and the molten metal stopped after 55% of the silica source was consumed. A gradual increase in mean MgAl2O4 crystallite size, D, from 24 to 36 nm was observed in the samples held for 10 h.en_US
dc.language.isoenen_US
dc.publisherIOP Publishingen_US
dc.subjectMgAl2O4en_US
dc.subjectReactive wettingen_US
dc.subjectStoichiometryen_US
dc.subjectConfigurational entropyen_US
dc.subjectDispersoid suspensionsen_US
dc.subjectInterfacial reactionsen_US
dc.titleMicrostructural development in Al/MgAl2O4 in situ metal matrix composite using value-added silica sourcesen_US
dc.typeArticleen_US
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