Scripta METALLURGICA
Vol. 2, pp. 327-329, 1958 Printed in the United States
ON THE KINETICS
OF STAGE III RECOVERY
IN COLD WORKED ~ T A L S
A. van den Beukel voor Metaalkunde, Technische The Netherlands
Labora~orium
Pergamon P r e s s , Inc.
Hogeschool,
Delft,
(Received April 10, 1968) The results metals
of the study of reaction kinetics
as found in the literature
can roughly
I) The point defect concentration c The isothermal cribed
annealing
in the stage III range o£ cold worked
be divided
c decreases
in two groups:
with
- exp -( ~)P
time according (I).
o curves of cold worked AI in stage lll can be very well des-
by this relation with p - 0,49 as has been shown by Frois
for Fe (Cuddy,
(2)) with p = 0,43.
p - 0,5 describes contains
obtained
2) According
density,
to Wintenberger
diffusion
of vacancies
which can be evalueted
in this way by Frois
the kinetics
(I) with
to dislocations.
The constant
from the experimental
(for instance
of interstitials
The result
(4),
to immobile
for this second order reaction,
tributed and have equal concentrations.
(I). The same is true
(3) the relation
results.
(I) seem reasonable.
to a second group of authors
annealing is due to the migration derived
According
the stress assisted
the dislocation
The values
to the equation
Waits
(6)
when both defects are uniformly
can be written
C O - 1 = Kit½ + K2t O
(5)) stage III
vacancies.
dis-
as follows:
(2)
wi th
K 1 - 8~½r2D½c c
o
(3)
K 2 - 4W/oDc o where
c = number of migrating c
o
=
the
same
at
D = diffusion r ° = capture combines
test
spontaneously
t
=
defects
0
coefficient
radius; with
per cm 3
of the migrating
an interstitial
defects
being at a distance ~ r ° from a vacancy
re-
the vacancy.
In (2) the first term dominates for short times, the second one for longer times. c the validity o f ( 2 ) u s u a l l y ~ - I i s p l o t t e d vs t ~ f o r s h o r t t i m e s and vs t f o r
longer times.
In both cases Stals and Nihoul
Nb. They conclude
that stage III recovery
of about 10 atomic distances, Recently
which
(5) obtain a straight
obeys equation
To
line for cold worked
(2). For r ° they obtain a value
seems to be rather large.
it has been noted by Cuddy
(2),
327
that the isothermals
of Stals and Nihoul
(5)
328
S T A G E HI R E C O V E R Y
IN C O L D W O R K E D
METALS
Vol. 2, No. 6
7Co_, C 6.
Y
I
i
T
Second
order
reaction
satisfying
for cold worked Nb, fitted
to equation
F I G . "I test to a set
equation
just as those of Schultz
(with their totally different
physical
points
(7) for W and of Martin
(I) with p values between 0,40 and 0,46.
why the same set of data can be described
description
of
(I) with p = 0,~
satisfactorily
backgrounds)
(8) for Mo can be
In this note we shall examine
by both equations
(I) and (2)
and how one can possibly
decide which
is the correct one.
First we have constructed curve was submitted
a curve satisfying
the rel~tion (I) with p = 0,5. This o to the second order test by plotting ~-- ~ I vs t. iThe result is
shown in fig.
I. After a small initial part which satisfies _~o c - I,-, t~ as follows from (I), for a large range of c_.. values a straight line is obtained. Figure I is remarkably c similar to the corrsspondin~ plot of Stals and Nihoul (5) for cold worked Nb. The plot of fig.
I seems good enough
to conclude
to second order kinetics,
which is clearly not
correct. After
series expansion
of the exponent Co c
equation
-i.(9)
(I) can be written as follows:
............ (4)
For not too long times the series can be cut off after equations
(4) and (2) have
the same form, which explains
data to both of them. The difference,
however,
the second
is that for the constants
K I and K 2 in (2) and (3) the relation can be deriveds 2
El
B = ~2 whereas
in (4) K I = ~ - ~
= 16r3c
term;
then
the 6cod fit of the experimental
(5)
O O
and E 2 = (2~) -I so that in this case B = 2.
of proportionalit7
Vol. 2, No. 6
S T A G E IH R E C O V E R Y
IN C O L D W O R K E D
METALS
329
From the isothermals of Stale and Nihoul (5) we find values of B between 2 and 3. From their analysis of the isochronal recovery of cold worked Nb, S~als, Nihoul and Gevers (9) conclude that the isochronal can be described by Waite second order kinetics with 4r5c = 1 or 0,25, giving B = 4 or 1. These authors argue that the first value o o is the correct one. The quoted values of B are, however, not sufficiently different from B = 2 to exclude the possibility that the recovery should be described preferentially by equation (1). At any rate the value of B is concentration dependent when equation (2) applies. Therefore it should be useful to measure the stage III reaction kinetics for different degrees of deformation corresponding to point defect concentrations differing by an order of magnitude. References
(1) c. Frois, Acta Met. 14, 1325 (1966). (~) L.J. Cuddy, Acta Met. !~6, 23 (1968). (3) M. Wintenberger,
Acta Met. I, 549 (1959).
(4) F. Ramsteiner, W. Sch~le and A. Seeger, Phys. Stat. Sol. ~, 937 (1964). (5) L. ~tals and J. Nihoul, Phys. Stat. Sol. ~, 785 (1965). (6) T.R. Waits, Phys. Rev. 107, 463 (1957). (7) H. Schultz, Acta Met. 12, 649 (1964). (8) D.G. Martin, Acta Met. ~, 571 (1957). (9) L. Stale, J. Nihoul and R. Gevers, Phys. Stat. Sol. 15, 717 (1966).