Formation of endogenous MgO and MgAl sub(2)O sub(4) particles and their possibility of acting as substrate for heterogeneous nucleation of aluminum grains

Aluminum containing 4wt.% magnesium was oxidized at a temperature for different oxidation times and analyzed by high-resolution electron microscopy. A thin oxidized layer of about 5 mu m, which is composed of MgO, forms at short oxidation time and gradually increases. High-resolution microstructures...

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Bibliographic Details
Published inSurface and interface analysis Vol. 47; no. 4; pp. 429 - 438
Main Author Kim, KeeHyun
Format Journal Article
LanguageEnglish
Published 01.04.2015
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Summary:Aluminum containing 4wt.% magnesium was oxidized at a temperature for different oxidation times and analyzed by high-resolution electron microscopy. A thin oxidized layer of about 5 mu m, which is composed of MgO, forms at short oxidation time and gradually increases. High-resolution microstructures reveal that the oxidized layers are porous regardless of oxidation time. After extended oxidation time, discrete MgAl sub(2)O sub(4) particles formed as a result of the reaction of initially formed MgO, liquid aluminum, and oxygen introduced from air through the porous MgO. Furthermore, it is clear by high-resolution lattice images that MgAl sub(2)O sub(4) particles are covered with thin Al sub(2)O sub(3), whereas MgO is bonded intimately to aluminum. Therefore, MgAl sub(2)O sub(4) particles that form naturally during oxidation are difficult to act as a direct substrate for nucleation of aluminum grains because of the coverage of Al sub(2)O sub(3). In contrast, MgO shows the possibility of acting as a substrate for the aluminum nucleation. The formation mechanism of MgO and MgAl sub(2)O sub(4) and their possibility of acting as substrates for nucleation of aluminum grains suggest that atomic level bonding and mismatches of nucleant/nucleus metal should be considered for correct evaluation of the possibility of heterogeneous nucleation of metallic matrix on a potent nucleant. Copyright copyright 2015 John Wiley & Sons, Ltd.
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ISSN:0142-2421
1096-9918
DOI:10.1002/sia.5726