Microstructure Based Creep Constitutive Model For Precipitation Strengthened Alloys: Theory and Application
Microstructure Based Creep Constitutive Model For Precipitation Strengthened Alloys: Theory and Application
Microstructure Based Creep Constitutive Model For Precipitation Strengthened Alloys: Theory and Application
:
cm ~rbug (5)
(ii) ug&Ge(b/rp)wplp; i.e. the glide rate within the
matrix is fast and the shear strain rate is
controlled by the rate at which climbing disloca-
tions are ‘released’ from the particle dispersion
and will be termed the dispersion controlled shear
:
creep rate cd=c
:
cd=c ~rb(b=rp )wp lp Ce (6)
h
Taking the interparticle spacing i square lattice
lp as the
spacing (Fig. 2) lp ~1:6rp (p=4w)1=2 {1 . Inserting lp
into equation (6), gives
2 Point obstacle representation of Fig. 1 illustrating the
: h i
stochastic ‘escape’ of climbing dislocations to enable cd=c ~1:6rb2 wp (p=4w)1=2 {1 Ce (7)
localised glide within matrix
Ge is given by Friedel9 for climb of a vacancy emitting
represented in Fig. 2 by the dotted ‘point’. It is a similar jog ‘e’ (see Fig. 1)
process to thermally activated glide below the athermal
threshold in the absence of diffusion and which has been cj Ds blp
termed ‘jerky glide’.8 There, a dislocation spends most of Ce,e ~ exp bt D {1 (8)
b2 kT
its time stationary but in this case, the ‘stationary’
fraction is in fact climbing and thereby continually where Ds is the volume diffusion coefficient cj the
providing a fresh concentration of potentially ‘glide dislocation line jog density blp is the slip activation area
active’ sites of the type represented by the dotted ‘point’. shown in Fig. 2 and btD, the force on the dislocation,
Climbing and gliding dislocation densities rc and rg where tD is given by tD ~tm {^tnet .
respectively are therefore not independent in this model For a vacancy absorbing jog, the jump frequency Ge,a
and the mobile dislocation density r is given by the is given by
following
cj D s blp
r~rc zrg (1) Ce,a ~ 2 1{exp{ btD (9)
b kT
The climbing dislocation density in contact with The number of vacancy emitting and absorbing jogs will
particles is rcwp and it is assumed that a fraction b/rp be approximately equal when the particulate micro-
will always be in a position to ‘escape’ from the set of structure is spherical or cubic, so the nett frequency Ge
particles after undergoing a single activated jump with will be given by the mean of equations (8) and (9), thus
frequency Ge, followed by localised glide within the
matrix. The dislocation glide density rg will therefore
cj D s tD b2 lp
increase at a rate rcwp(b/rp)Ge but will be immobilised Ce ~ 2
sinh (10)
temporarily at the next particle at a rate rgug/lp, where b kT
rgug is the gliding flux and lp the interparticle spacing. The dispersion controlled shear creep rate within the
: :
Their net rate of increase rg is therefore given by matrix cd=c is given by substituting equation (10) into
: ug equation (7)
rg ~rc wp (b=rp )Ce {rg (2)
lp h i
: tD b2 lp
Equation (2) can be integrated after substituting for rc cd=c ~1:6rwp (p=4w)1=2 {1 cj Ds sinh (11)
kT
using equation (1), with rp and wp constant and setting
rg50 at t50 to give An important point to note that the dispersion term lp is
in the sinh function of equation (11) and therefore very
Ce (b=rp )wp lp sensitive to stress. Particles coarsen with time and so the
rg ~r
ug zCe (b=rp )wp lp rate of change of lp becomes an important factor in
predicting long term performance. The pre sinh term
ug zCe (b=rp )wp lp depends only on volume fraction wp which remains
1{exp { t (3)
lp constant during standard isothermal creep tests, but
decreases with temperature. The change of wp with
The term in square brackets is a transient and will be
temperature requires quantification in order to predict
neglected, giving the following matrix dislocation glide
behaviour at different temperature levels and/or under
flux
variable temperature conditions.
Ce (b=rp )wp lp
rg ug ~ rug (4) Microstructure based equation set
ug zCe (b=rp )wp lp
Equation (11) needs to be expressed in terms of tensile
There are two limits to equation (4) stress and strain in order to analyse the uniaxial datasets
(i) Ce (b=rp )wp lp &ug , i.e. the glide rate within the given in the following section. Standard relationships
matrix is slow and rg increases until can be found in the literature for a polycrystal loaded
rg %r (rc %0) and the matrix shear creep rate under uniaxial tension, giving the dispersion controlled
: :
cm (~brg ug ) is given from equation (4) by tensile strain rate ed=c
h i
: 1:6 1=2 sD b2 lp
ed=c ~ rwp (p=4w) {1 cj Ds sinh (12)
M- MkT
-
where M - is the Taylor factor (%3) and sD ~sm {^snet .
To be of practical use, equation (12) has to be an
explicit function of applied stress s. The method used to
achieve this (i.e. going from the microstructural scale to
the macro or global scale) is developed in the section on
‘Appendix’, based on the work of Ion et al.10 There are
two issues to consider:
(i) the relationship between the local creep rate in
one of the phases and the global creep rate that is
measured in the laboratory
(ii) the necessary transfer of load from weaker to
stronger parts of the microstructure – in this case 3 Comparison of measured volume fraction of gamma
from creeping matrix to elastic particles – and its prime in laboratory prepared In 597 as function of tem-
associated kinetics, along with the mechanism perature with model fit using equations (18) and (19)
and mechanics dictating the magnitude of load
partition. 20 000 h over a range of temperatures.12 These data can
The global creep rate for the dispersion controlled be represented by the following empirical relationship
mechanism is given in equation (30) in the section on
3 3 3|105
‘Appendix’ r ~ri zexp { (17)
RT
: 1:6 h i
eG ~ rwp (1{wp ) (p=4w)1=2 {1 As particle sizes increase, there will be a proportionate
M- increase in |lp| and thus an increasing creep rate,
" #
(s{si {^snet )b2 lp equation (13).
cj Ds sinh (13)
MkT
- Volume fraction of c9
The standard commercial heat treatment of Nimonic 90
where sD has now been replaced by the applied stress s
consists of solution treatment at 1080uC with an ageing
and an internal stress si which has the following
treatment at 700uC for 16 h. The c9 solvus temperature is
evolution equation, derived in equation (33) in the
approximately 1000uC and the mechanical data dis-
section on ‘Appendix’
! cussed below ranges from 600 to 900uC. Since the c9
: wp E si : volume fraction occurs in the pre sinh of equation (13)
si ~ 1{ 1 eG (14) and also indirectly through the |lp| in the sinh function,
1{wp si an analytical expression for the temperature dependence
1
The upper bound value for internal stress si is given by of wp becomes an important requirement. An indirect
method will be presented since no published data were
equation (32) in the section on ‘Appendix’
found in the literature.
1 2wp Figure 3 is from Gibbons and Hopkins13 and shows
si ~ s (15) c9 volume fraction as a function of temperature in a
1z2wp
laboratory alloy based upon commercial IN597. The
Two further evolution equations are required: one for following lever rule equation used here to fit the data
the dislocation density r and another for the inter-
particle spacing lp. The dislocation density appears C0 {Ce (T)
wp (T)~ : (18)
directly in the pre sinh term of equation (13) and 0 23{Ce (T)
indirectly through the network strength term in the sinh where C0 is the concentration of the main c9 forming
function. They act in opposition. Since the initial elements in the alloy and Ce(T), their summed equili-
magnitude of ^snet is of order unity in superalloys – brium matrix solute concentration, given by
because of low initial dislocation densities – and the
7250
applied stresses are usually several hundred MPa, there Ce (T)~17exp { (19)
is invariably a net increase in creep rate due to increasing T
dislocation density, at least in the early stages of creep. At the solvus, wp(T)50 and so C05Ce(Ts) in equa-
There is still no universally accepted equation for the tion (18), where Ts is the solvus temperature.
evolution rate of dislocations in superalloys, so the Substituting C05Ce(Ts) into equation (19) gives the
empirical one suggested by Dyson and McLean11 will be following equation for Ts
used here
: : 7250
r~K e (16) Ts ~ (20)
ln(17=C0 )
where K5300ri The solid line in Fig. 4 is a plot of solvus temperature as
Equation (16) takes no account of the kinetics of a function of C0 given by equation (20). Experimental
trapping or annihilation (by climb processes). data from several superalloys are in good agreement
Coarsening occurs in c9 dispersions and average considering that only a three parameter model has been
particle size data for Nimonic 90 are available up to used. Nimonic 105 has been included to illustrate the
Creep lifetimes
Figure 7 shows rupture lifetime as a function of stress
for Nimonic 90, again using the same digitised database
from the paper by Harrison and Evans.15 Predicted
creep curves are shown as solid lines and were generated
by numerically integrating the same constitutive equa-
tion set used in the previous section, but under constant
load. The lifetime database covers a larger temperature
range than was the case with minimum creep rates. The
two lowest temperatures – where no corresponding 7 Comparison of industry generated rupture lifetime data
minimum creep rate data were supplied – are remark- in temperature range 600–900uC, with predictions of
ably well predicted, particularly the database at 650uC, dispersion controlled creep model
which extends to 20 000 h duration.
Short term lifetimes are also well represented at all necessary to perform pretreatment and subsequent creep
temperatures by the model but not longer lifetimes at tests at the same temperature in order to avoid other
temperatures .700uC. The shortfalls in predicted life- potential changes in microstructure.
time clearly become systematically larger as tempera- The dispersion controlled creep equation (13) has
tures increase. successfully predicted the steep decline in 0?1% proof
stress data at temperatures .700uC. Below 700uC,
Discussion calculations using equation (20), demonstrate that
particle shear truncates the field of activity of creep
The microstructure based kinetic creep equation (13), controlled yielding. Nimonic 90 is therefore weaker at
has been termed ‘dispersion controlled’ because creep lower temperatures than it would have been had shear
rates are predicted to be highly sensitive to changes in not intervened. The value used for capb in computing ^sc
the dispersion parameter lp the interparticle spacing. is higher than the usual range quoted, 0?1–0?2 J m22,
Particle coarsening is an important feature of most, if but is similar to the maximum of 0?3 J m22 measured by
not all, alloys in service. To date, its influence on service Raynor and Silcock,16 who studied a number of low
lifetimes has never been quantitatively assessed, quite volume fraction nickel base alloys.
possibly because no creep law explicitly contains the If the rapid decline in proof stress of Nimonic 90
parameter lp; a necessary requirement. Testing the beyond 700uC is a consequence of dispersion controlled
predictions of equation (13) becomes, therefore, very creep, then proof stress data should be dependent upon
important for assessing its validity. To that extent, the the magnitude of the testing strain rate: the faster the
results presented in Fig. 6 are a disappointment. The imposed strain rate, the higher the Proof Stress.
progressive increase in the magnitude of shortfalls in
predicted lifetime as temperatures rise could be inter-
preted as being the consequence of gross overestimates Conclusions
of the effect of coarsening; thereby essentially condemn- 1. The derived ‘dispersion controlled’ creep rate
ing the dispersion controlled model. However, in (equation (13)) is characterised by its high sensitivity
mitigation, it is also observed that minimum creep rates to the magnitude of interparticle spacing. The creep data
in Fig. 7 progressively overestimate creep rates at higher available in this work was isothermal and has proved
temperatures, suggesting that the cause of progressive inadequate for testing this prediction unambiguously.
shortfalls in lifetime may be related to small errors in This is a consequence either of equation (13) being
initial parameter values within equation (13). Creep wrong or because of small uncertainties in the magni-
rates and lifetimes are inextricably linked. Additionally, tudes of initial parameters in equation (13) and/or in the
there may be errors in the parameter input into the evolution laws. Preaging tests are suggested as being the
empirical dislocation multiplication process. A more best way of establishing whether equation (13) ade-
systematic and rigorous computational effort than quately describes long term behaviour in Nimonic 90.
performed here would be needed to establish or deny 2. Proof stress calculations predict that the rapid
this unambiguously. decline in experimentally determined values at tempera-
A much better and conclusive method would be tures .700uC is a consequence of yield being due to
experimental. Equation (13) predicts that a thermal dispersion controlled creep. If true, then proof stress
treatment of Nimonic 90 under zero load would result data should be dependent upon testing speed. Below
in a subsequent increased creep rate when compared to 700uC, proof stress should be independent of testing
the as received alloy, tested under the same stress. speed, since the particle cutting mechanism is athermal.
Figure 6 suggests that a temperature of 750uC would be
sufficiently high to ensure the need for only relatively Acknowledgements
short pretreatment times. There is anecdotal evidence
that similar testing in other nickel base superalloys does Many thanks are due for many fruitful discussions with
indeed reduce creep resistance. In this case, it would be several colleagues over the years: in particular, Doctor
easily found using the definition of si (;s2sm) and fields would ‘harden’ the matrix, as Pollock and
1 1
equation (25) with sp ~3sm Argon17 have pointed out for very high volume
fraction superalloys (wc’ %70%). Any of the above
1 2wp stress controlled mechanisms may intervene before si
si ~ s (32) 1
1z2wp reaches si . This will become more likely at
1 1 lower temperatures/stronger alloys because the larger
Thus si and therefore sm are proportional to s through stresses involved will favour a stress controlled inter-
a microstructural term f(wp). Equation (32) contrasts vention.
with the one given by Ion et al.,10 which assumed It is likely that there will be a spectrum of critical
diffusion creep to be the stress relaxation mechanism internal stresses within the microstructure – reflecting
and is therefore potentially the lower bound stress local differences in volume fraction for example – rather
controlled mechanism. 1
than a unique value si . A stochastic approach to si
The implicit assumption here is that the strain fields evolution seems therefore to be appropriate and a simple
between particles do not interact significantly. At best, 1{si
this would limit the use of equation (32) to low volume empirical probability function 1
si
has been used to
fraction alloys – a simple slip line argument suggests transform equation (31) into the following
less than 20–30% volume fraction. For larger volume !
1
fractions, si would be expected to be greater than : wp E si :
si ~ 1{ 1 eG (33)
given by equation (32) because the interaction of strain 1{wp si