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ABSTRACT
There have been a number of
procedures
reported
for
the
prediction of physical properties of
aluminum based on cooling rate data.
One of the most common is the
cooling rate calculation procedure
described by Fink and Willey in
their
now-classic
work
on
7075
characterization.
Staley has more
recently
described
the
use
of
"Quench Factor Analysis" (QFA) to
better predict various properties of
aluminum which is the subject of
this paper. A discussion of the
principles of the calculation
and
the experimental procedure used for
QFA determination from cooling curve
data will be provided here.
The
generation of the multiparametric CT
function from cooling curves will
also be discussed.
C.E. Bates
reported
earlier
by
Willey
illustrating
the
critical
temperature range for the transition
of
pitting
to
intergranular
corrosion for 2024.[3]
Various studies were conducted
after Fink and Willey's work to
determine the relative quench rate
sensitivity to yield
different
properties
for
various
alloys.
Figure 3 illustrates the effect of
cooling rate on tensile strength for
different
aluminum
alloys
and
tempers.[2]
INTRODUCTION
Fink and Willey performed an
extensive study on the effects of
quenching on the strength of 7075-T6
and corrosion behavior 2024-T4.[1]
This was done by constructing Ccurves which were plots illustrating
the times required to precipitate
sufficient alloy content to change
the strength by a certain amount
(7075) or change the corrosion from
pitting to intergranular (2024). The
"critical temperature range", that
temperature range that provided the
highest
precipitation
rates
was
identified.[2] Figure 1 illustrates
Fink and Willey's C-Curve for 7075.
Figure 2 is a C-Curve similar to one
DISCUSSION
Calculation of Quench Factors from
Precipitation Kinetic Data
The properties of aluminum
alloys are dependent on the amount
of alloy precipitation that occurs
during cooling. The rate law for
isothermal
precipitation
kinetics
is:[5]
(1)
where:
is
the
fraction
of
precipitation which has occurred in
time (t) and k is a temperatureindependent constant. The value of k
depends
on
the
degree
of
supersaturation and the rate of
diffusion and is estimated from:[6]
Figure 3 - Tensile strength
function average cooling rate.
as
(2)
where:
CT
= critical time required
to
precipitate
a
constant
amount (the locus of the
critical
line
is
the
Ccurve).
k1 = constant which equals the
natural
logarithm
of
the
fraction untransformed (1 fraction defined by the Ccurve).
k2 = constant related to the
reciprocal of the number of
nucleation sites,
the C-curve.
As illustrated in Figure 4
[5],
the
quench
factor
()
is
obtained by combining the cooling
curve for the quenching process with
the C-curve and the value for is
obtained by:[2]
R = 8.3143 J.K-1.mol-1
(5)
T = temperature in oK.
From these relationships, it
is possible to redefine the equation
for
the
amount
of
solute
precipitated during the quench ()
which can be calculated :[2]
(3)
Cahn
has
shown
that
the
transformation
kinetics
for nonisothermal conditions, such as those
that would be present during a
typical quenching process, may be
described by: [6,7]
(4)
where:
CT = critical time from the Ccurve,
t = time from the cooling
curve,
t0 = time at the start of the
quench,
tf = time at the finish of the
quench,
= measure of the amount
transformed (quench factor).
When =1, the fraction transformed
equals the fraction represented by
(6)
(7)
Effect of Time Step (t) Selection
In order to determine the
effect of the size of the time step
on the quench factor calculation,
the quench factors for 7075-T73
quenched in 100oF (38oC) water at 50
ft/min (0.25 m/s) was studied.
The results of this study are
shown in Table 1. These data show
that time step changes in the range
of 0.1 to 0.4 seconds caused no
appreciable change in the calculated
quench factor.
However, time step
variations
between
0.5
to
0.8
seconds caused considerable scatter
in the calculated quench factor (Q).
Excessively long time steps may
result in an inadequate number of
data points to properly calculate
transition in the critical portion
(knee)
of
the
C-curve.
It
is
suggested
that
the
time
step
interval should be selected such
that the average temperature drop is
not greater than 75oF (25oC) over the
critical cooling range for the alloy
of interest.
Table 1
Effect of Time Step Magnitude on
Quench Factor Calculation
Property Calculation
(8)
where:
K1 = ln (0.995) = -0.00501
Q = quench factor
The
relationship
between
quench factor and yield strength for
7075-T73 is shown in Figure 7.[8]
Figure
7
Yield
strength
of
aluminum 7075-T73 as a function of
quench factor of the material.
Low values of Q are associated
with high quench rates, minimum
precipitation
during
cooling and
high yield strengths. Conversely,
higher Q-values are obtained with
slower
quench
rates
and
are
associated
with
lower
strength
values.
corrosion,
stress
exfoliation.
corrosion
or
Experimental Apparatus
The quench factor provided by
a
particular
quenchant
can
be
determined
experimentally
using
parts or probes instrumented with
thermocouples
and
a
testing
apparatus in which the quenchant
concentration,
flow
rate,
and
temperature can be controlled. In
principle, any quenchant bath could
be used, including the commercial
bath used in practice. Figure 8
illustrates one system that has
performed
well
in
the
laboratory.[10]
However,
it
is
important to note that different
agitation
systems
will
yield
different results due to differences
in the directionality and turbulence
of fluid flow.
An illustration of a bar and
sheet probe used for laboratory
testing is provided in Figures 8 and
9 respectively.[10] A computerized
data acquisition system is used to
collect
and
store
the
timetemperature
data
from
the
instrumented probes or parts during
quenching.[11]
Figure
8
Illustration
of
a
laboratory quench bath capable of
providing a controlled uniform flow
rate
at
a
temperature.
reasonable
constant
Figure 13 (Reference 7)
C-Curve
for
6351-T6.
Table 2
7. J.T.
Analysis
Materials
1987, Vol.