structural transitions during leaching of Ni2Al3 phase in a Raney Ni-Al alloy

The microstructure transitions during leaching of a rapidly solidified Ni-Al alloy have been investigated by means of X-ray diffraction, transmission electron microscopic (TEM) and high resolution electron microscopic (HREM) techniques. Ni₂Al₃ was the main phase in the starting Ni-Al alloy. The micr...

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Bibliographic Details
Published in:Journal of materials science Vol. 36; no. 23; pp. 5649 - 5657
Main Authors: Wang, Rong, Lu, Zhilong, Ko, Tsun
Format: Journal Article
Language:English
Published: Heidelberg Kluwer Academic Publishers 01-12-2001
Springer
Springer Nature B.V
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Summary:The microstructure transitions during leaching of a rapidly solidified Ni-Al alloy have been investigated by means of X-ray diffraction, transmission electron microscopic (TEM) and high resolution electron microscopic (HREM) techniques. Ni₂Al₃ was the main phase in the starting Ni-Al alloy. The microstructure of the Raney nickel catalyst consists of nano-scale nickel crystallites, residue of source phases surrounded by nano-scale boundary regions. The transformation during leaching of Ni₂Al₃ phase was an advancing interface type process. Clusters of AuCu-structure type face-centrered tetragonal Ni₃Al₂ as an intermediate phase seems to appear in the reaction front. Based on an analysis of the atomic configurations of phases Ni₂Al₃, Ni₃Al₂ and nickel, a reasonable explanation for the transition mechanism during leaching of Ni₂Al₃ phase and the arc characteristic of diffraction spots was proposed. The nickel crystallites generated during leaching obey an orientation relationship with the source Ni₂Al₃ phase, which is consistent with the Delannay's orientation relationship proposed for nickel and NiAl phases. The nano-scale structural characteristic of the Raney nickel catalyst, especially its porous structure at the boundary regions, provides an excellent hydrogenation catalytic activity and selectivity of the catalyst.
Bibliography:http://dx.doi.org/10.1023/A:1012578002418
ObjectType-Article-2
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0022-2461
1573-4803
DOI:10.1023/A:1012578002418