Vol. 9, pp. 75-78, 1975 Printed in the United States
ScriptaMETALLURGICA
ORDERING AND TENSILE DUCTILITY W. N. Roberts*
Pergamon
Press,Inc.
IN A Ti-AI-Ga ALLOY%
and M. J. Godden**
*Head, Metal Physics Section and **Research Scientist, Engineering Physics and Refractory Metals Section, Physical Metallurgy Division, Mines Branch, Department of Energy, Mines and Resources, Ottawa, Canada. (Received November In titanium-aluminum forms by a first-order
18, 1974)
binary alloys,
transformation.
the ordered phase Ti3AI
The single-phase
from 21 at.%Al to 37 at.%Al at 700°C(I).
(~2 type)
field of Ti3AI extends
In the ~ - T i + ~
phase field, ordering
to produce ~2 can be suppressed by rapid quenching when the aluminum content is low.
However,
a long-range
above about 18 at.%Al,
order parameter
ordering cannot be suppressed
approaching
unity at room temperature
Fully-ordered
Ti3AI has limited ductility,
cleavage-type
failure mode.
fracture
surfaces
The lack of significant
Ti3AI , DO19, exhibits
Several workers(4-7)
at.%Ai-7.41
of slip in directions
However Mg3Cd , which is the same structure good ductility
in the fully-ordered
have modified
alloys with ternary element additions characteristics.
the composition
~2 alloys to be brittle, in compression
at.%Ga was ductile
however the alloy
because a second phase
the intense planarity of slip and increased the occurrence In earlier work(6),
sition 12 at.%Al-12 quenching
12.19
Williams et al(5) have re-
12.5 at.%Al-12.5 slip.
of the binary Ti-AI
Hoch et al(4) have reported an alloy of the composition
ported several ternary single-phase
~
type as
condition(3).
in an attempt to modify the deformation
at.%Ga to be single phase and ductile.
Ti2Ga decreased
showing a largely
ductility has been attrib-
uted to the severe planarity of slip and the difficulty other than (2).
and a2 with is found.
we have reported an alloy having the compo-
at.%Ga to be ductile
from 1300°C.
of
in tension at room temperature
after
This work reports the result of aging heat treatments
on this alloy composition. The alloy was melted and worked in a similar manner to that previously reported(6).
Specimen blanks were solution treated
in the B~hase
field at
1300°C in a vacuum of less than 1.3 x 10-4pa for 4 hr and quenched by dropping out of the hot zone into a flowing helium gas stream. rate was 60°C/sec.
After machining
to avoid any possibility
of contamination,
vacuum of 6.5 x 10-4pa for 5 hr at various # Crown Copyright
The approximate
0.5 mm from the surface of the
Reserved. 75
quench
gage length
specimens were aged in a dynamic temperatures
and oil-quenched.
76
ORDERING IN A TI-AI-Ga ALLOY
they were subsequently the results
Vol.
9, No. I
tested in tension at a strain rate of 2 x 10-4sec-l;
are presented
in Table i. TABLE1
Tensile Behavior of Alloy Aged at Various Temperatures Aging Temperature,
0.2% Yield Stress, MPa
°C
As quenched
U.T.S.,
Elongation, %
MPa
648
759
21
200
596
688
21
300
869
893
4
400
807
827
5
500
761
786
5
600
662
666
4
It can be seen that the ductility
shown by this alloy after quench-
ing from the 8-phase field is largely lost when it is aged for 5 hr above 200°C, although the alloy is not completely brittle An examination by transmission the as-quenched
condition,
~ith weak antiphase
Fig.
after quenching long-range
showed no "anomalous
film of the e solid solution(l).
diffraction
spots was also detected,
contrast" The presence
indicating
that even
some level of
order.
Gehlen(8)
any estimation
of the long-range
order parameter
shows that the atoms are slightly displaced
sites in Ti3AI and a similar effect would be expected displacements
would radically change the relative
it is believed that in the as-quenched
condition
is diffi-
from the lattice
in ternary e2"
intensities
spots, making an estimate of the degree of long-range ordered,
e2
such as Ti2Ga, was
from the 8-phase field, the alloy has developed
However, cult.
to be single-phase
No second phase,
domain boundaries
associated with a thin, trapped of weak superlattice
electron microscopy of the alloy in
I, shows the structure
domain boundaries.
observed and the antiphase
in this condition.
These
of the observed
order difficult.
However,
this alloy is only partly
the gallium tending to retard the kinetics of the ordering process.
Shamblen and Rosa(9)
have shown that in s-titanium,
the diffusion
coefficient
for gallium is lower than for aluminum and the activation energy for diffusion is higher for gallium than for aluminum. fusion-controlled,
retention of some disorder ternary additions
Since the ordering process
is dif-
the reduced rate of gallium diffusion could permit the on quenching.
Also, Crossley(7)
tend to slow the formation of ~2"
the lowering of the degree of long-range
has found that some
It would be expected that
order would reduce the antiphase boun-
dary energy which would permit easier cross-slip.
The significant
ductility
shown by specimens aged below 300°C is attributed to enhanced cross-slip.
Vol.
9, No. I
ORDERING IN Ti-AI-Ga ALLOY
77
When aging below T c (estimated to be somewhat below 640°C for this alloy(10)), diffusion permits the degree of long-range order to increase,
causing
the dramatic decrease in ductility for aging temperatures at 300°C and above. Further diffusion causes the growth of domains by the annihilation of antiphase domain boundaries
in a manner analogous to grain growth.
decrease in yield strength as the aging temperature
This results in a
is increased,
a result
similar to that obtained by Blackburn(2). A similar alloy prepared using titanium sponge stead of crystallette titanium
(oxygen <0.01 wt%)
as a base material,
ductility after quenching from the 8-phase field. that oxygen tends to stabilise the ~2 phase.
(oxygen 0.053 wt%)
in-
showed no
This observation suggests
Namboodhiri e~ al(ll)
found that
oxygen stabilised Ti3AI to higher temperatures in two-phase alloys, which would support this view. REFERENCES i.
M. J. Blackburn,
2.
M. J. Blackburn and J. C. Williams,
3.
N. S. Stoloff and R. G. Davies,
4.
M. Hoch, J. V. Hackworth, R. J. Usell and H. L. Gegel, The Science, Technology and Application of Titanium, Eds. R. I. Jaffee and N. E. Promisel 359, Pergamon Press (1970).
5.
J. C. Williams and M. J. Blackburn, Ordered Alloys, Eds. B. H. Kear, C. T. Sims, N. S. Stoloff, and J. H. Westbrook, 425, Claitor's Publishing (1970).
6.
M. J. Godden and W. N. Roberts, Titanium Science and Technology, R. I. Jaffee and H. M. Burte, 2207, Plenum Press (1973).
7.
F. A. Crossley,
8.
P. C. Gehlen, The Science, Technology and Application of Titanium, R. I. Jaffee and N. E. Promisel 349, Pergamon Press (1970).
9.
C. E. Shamblen and C. J. Rosa, Met. Trans.
i0. E. W. Collings, and Technology,
Trans. AIME 239, 1200
Met. Trans.
(1967).
Trans. ASM 62, 398
Trans. ASM 57, 247
i, 1921
(1969).
(1964).
Eds.
(1970).
2, 1925
Eds.
(1971).
J. E. Enderby, H. L. Gegel and J. C. Ho, Titanium Science Eds. R. I. Jaffee and H. M. Burte, 801, Plenum Press (1973).
ii. T.K.G. Namboodhiri,
C. J. McMahon and H. Herman, Met. Trans.
4, 1323
(1973).
78
ORDERING IN A Ti-AI-Ga ALLOY
FIG.
Vol.
1
Antiphase domains in a Ti-12 at.% AI-12 at.% Ga alloy. Dark field taken with a (2110)~ 2 reflection. Zone axis
[Olil] ~2"
9, No.
i