Hostname: page-component-78c5997874-g7gxr Total loading time: 0 Render date: 2024-11-05T08:52:19.646Z Has data issue: false hasContentIssue false

AEM Analysis of Grain Boundary Segregation and Precipitation in Al-Mg Alloys

Published online by Cambridge University Press:  02 July 2020

J.S. Vetrano
Affiliation:
Pacific Northwest National Laboratory, Richland, WA99352USA
S.M. Bruemmer
Affiliation:
Pacific Northwest National Laboratory, Richland, WA99352USA
Get access

Extract

Magnesium is an important and common solid solution strengthening agent for aluminum alloys. It has been known for many years that Mg segregation to grain boundaries (GBs) and other structural inhomogeneities can lead to precipitation of the ² (Al3Mg2) phase during low-temperature aging. This phase is anodic with respect to the matrix so its presence degrades the stress corrosion cracking (SCC) resistance of the alloy. The details of P-phase precipitation have been studied in detail in binary Al-Mg alloys [3-5] but there is some indication that ternary elements can alter the precipitation kinetics and spatial distribution which in turn will affect SCC. Therefore we are studying the segregation and precipitation of Mg in a commercially important Al-Mg alloy which contains Mn and Cr as grain refining particles.

Specimens were prepared from a commercial 5083 heat with the composition 4.47% Mg, 0.61% Mn, 0.08% Cr, 0.09% Si, 0.21% Fe, 0.05% Cu, bal. Al (all compositions in weight percent). Following cold rolling they were given a recrystallization anneal of 10 min. @ 500°C and air cooled.

Type
Segregation and Diffusion Analysis in Materials
Copyright
Copyright © Microscopy Society of America 1997

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

1.Eikum, A. and Thomas, G., Acta Met., 12 (1964) 537.10.1016/0001-6160(64)90026-4CrossRefGoogle Scholar
2.Cundy, S.L.et al., Proc. Roy. Soc. A, 307 (1968) 267.Google Scholar
3.Malis, T. and Chaturvedi, M.C., J. Mat. Sci. 17 (1982) 1479.10.1007/BF00752263CrossRefGoogle Scholar
4.Paine, D.C., Weatherly, G.C. and Aust, K.T., J. Mat. Sci., 21 (1986) 4257.10.1007/BF01106539CrossRefGoogle Scholar
5.Perryman, E.C.W. and Hadden, S.E., J. Institute of Metals, 77 (1950) 207.Google Scholar
6.Hamana, D.Nebti, S. and Hamamda, S., Scripta Met. et Mat 24 (1990) 2059.10.1016/0956-716X(90)90486-ZCrossRefGoogle Scholar
7. This work supported by the Materials Division, Office of Basic Energy Sciences, U.S. Department of Energy under Contract DE-AC06-76RLO 1830.Google Scholar