Stress corrosion cracking (SCC) of rapidly solidified magnesium-alumin
um alloys in aqueous solutions of potassium chromate and sodium chlori
de was investigated using electrochemical techniques, constant displac
ement rate tests, and optical and electron microscopy. Microcrystallin
e alloys containing 1 and 9 wt% aluminum were prepared using a melt-sp
inning process which yields continuous ribbons 15-25 mum thick. Potent
ial-pulse and scratched electrode experiments showed that repassivatio
n kinetics are improved both by rapid solidification and increased alu
minum content. The melt-spun alloys experienced relatively uniform att
ack, and repassivated more rapidly and more completely than their as-c
ast counterparts. Both failed by transgranular stress corrosion cracki
ng (TGSCC) in aqueous 0.21M K2CrO4 containing 0.6M NaCl at displacemen
t rates between 5 x 10(-5) and 9 x 10(-3) mm s-1. In 0.6M NaCl, TGSCC
occurred only near 3.6 x 10(-3) mm s-1, while no stress corrosion was
observed in chromate solution without chloride. Constant displacement
rate tests in air after pre-exposure to the electrolyte indicated that
TGSCC probably results from a hydrogen embrittlement process. Using r
easonable estimates of the diffusivity of hydrogen in magnesium, analy
sis of the constant displacement rate and potential-pulse tests for Mg
-9Al supports a model involving the formation of magnesium hydride ahe
ad of the crack tip.