MSE 230
Spring 2010
1. (a) From Fig. 10.11, the curve for recrystallization at 119C is closest to 95% recrystallized in 60 min. (118C would be acceptable, although this level of precision is not practical. (b) i) Impurities in solution usually decrease diffusivity and thereby increase the temperature required for a given degree of recrystallization in a given time; ii) the higher the %CW the higher the driving force (energy difference) for recrystallization and thus the lower the recrystallization temperature. 2.
(a)
(a) 100% P (b) 75% P + 25% M* (c) ~50% M + 50% A** (d) ~100% M* (e) 100% B *M in (b) and (d) contains 5% retained A (i.e., M transformation is 95% complete at RT) **Cooling from 175C, the remaining A would transform to M, the extent of which depending only on decrease in temperature.
(b)
(c)
(a, b, d, e)
3.
(b) (c) (c) (b) (a) (d)
(c)
(a) Fine pearlite and proeutectoid ferrite (b) Martensite (c) Martensite and proeutectoid ferrite (d) Coarse pearlite and proeutectoid ferrite (e) Martensite, fine pearlite and proeutectoid ferrite. Note that martensite + ferrite would be produced under any cooling rate between curve (b) and (c) shown. Cooling rates faster than (c) would yield less ferrite and more martensite. Note that the austenitization temperature is higher than for an eutectoid steel. See the phase diagram to make sure you understand why.
(c) (b)
(e) (a)
(d)
2010 KPTrumble
4.
Hardness
(strength)
of
(b)
>>
(c)
>
(e)
>
(a)
>
(d),
in
the
order
of
decreasing
cooling
rate.
The
rank
order
of
hardness
of
the
microstructure
constituents
is
M
>>
Pfine
>
Pcourse
>>
F.
The
hardness
of
the
structures
containing
multiple
constituents
(all
except
b)
will
be
some
weighted
average
of
the
hardness
of
the
constituents.
Note,
whenever
the
A
=>
F
transformation
is
complete
(cooling
rate
(c)
and
slower)
the
proportion
of
ferrite
in
the
structure
is
the
same,
as
given
by
the
phase
diagram
(wF=0.55).
With
decreasing
cooling
rate,
the
balance
of
the
structure
(0.45)
is
softer
(from
all
M
to
M
+
Pfine,
to
all
Pfine,
to
Pcoarser),
so
the
overall
hardness
must
likewise
decrease
with
decreasing
cooling
rate.
Any
structure
that
contains
any
amount
of
pearlite,
must
also
contain
this
amount
(0.55)
of
primary
ferrite.
5.
Product
2(d)
is
Bainite,
which
when
formed
at
250C
in
a
1080
steel
has
a
hardness
of
550
Brinell
(Fig.
10.31).
Product
2(e)
is
Martensite.
Using
the
tempering
data
in
Fig.
10.35
(right),
only
the
315C
tempering
kinetics
line
allows
tempering
to
a
hardness
of
550
Brinell
in
the
time
range
covered
by
the
data
(~10
s
to
~1
day).
Tempering
for
a
little
over
one
hour
(3800
s)
would
soften
(and
toughen)
the
martensite
to
a
hardness
of
550
Brinell.
6.
The
temperature
versus
time
plot
of
the
solution-treatment
and
aging
cycle
is
shown
on
the
next
page.
In
the
solution-treatment
process,
the
coarse
phase
(CuAl2)
dissolves
into
the
phase
(Al-Cu
solid
solution).
Eventually
(at
equilibrium)
the
is
a
uniform
solid
solution
of
4.4
wt.%
Cu
in
Al.
It
is
important
to
stay
below
the
solvus
temperature
to
avoid
liquid
formation
during
solution
treatment.
Staying
below
the
eutectic
temperature
ensures
that
any
local
regions
of
higher
Cu
concentration
(due
to
segregation
from
solidification)
will
not
remelt.
The
precipitates
that
forms
at
the
usual
aging
temperatures
have
the
composition
CuAl2,
but
slightly
different
crystal
structure
than
the
equilibrium
,
hence
the
designation
.
The
hardness
rises
as
their
number,
size
and
volume
fraction
increases.
At
204C,
the
maximum
hardness
is
reached
in
about
1
to
2
h.
With
continued
aging,
the
precipiates
coarsen,
with
the
larger
ones
growing
and
the
smaller
ones
shrinking
away
(driven
by
the
decrease
in
interface
area).
Thus,
their
number
decreases
and
spacing
increases,
so
the
hardness
drops
(overaging).
The
main
advantage
of
aging
at
lower
temperatures
is
that
the
peak
hardness
(strength)
increases.
At
lower
temperatures,
the
driving
force
(undercooling)
for
nucleation
is
higher,
producing
more
precipitates
and
thus
a
smaller
spacing
between
them,
more
effectively
impeding
dislocation
motion.
The
disadvantage
is
that
the
time
to
reach
the
peak
hardness
is
longer,
about
a
day
at
150C
(in
this
case,
the
relative
peak
hardness
increase
is
small).
2010 KPTrumble
T(C)
Solution-Treatment, 525C/1 h +
+ -CuAl2
TEutectic = 548C
Quench
100 (supersaturated)
time