Professional Documents
Culture Documents
Prantil
M. L. Callabresi2
J. F. Lathrop2
Sandia National Laboratories,
Livermore, CA 94551-0969
G. S. Ramaswamy
The General Electric Company,
Niskayuna, NY 12309
M. T. Lusk
Colorado School of Mines,
Golden, CO 80401
Introduction
During heat treatment, furnace and quench schedules produce
complex thermal histories in which parts simultaneously experience significant thermal as well as phase transformation-induced
volume changes. The complex interaction and relative timing of
these competing factors determine the residual stresses and displacements that result. Often thermal processing results in detrimental shape changes. Examples include helical unwinding and
potato chipping in quenched gears and plate warping in multipass
welding. While beneficial residual stresses can be tailored, conditions do arise in which internal stresses are sufficient to cause
fatigue and quench cracks. For parts with complex shapes, undesirable residual stresses can also result from locally constrained
deformation.
In the austenitic, low carbon steels of interest in this work,
successful analysis of these processing steps requires an accurate
material characterization and constitutive description of the material. When quenching low alloy steels, the thermal and mechanical
responses are inherently coupled with evolution of the underlying
material microstructure. In particular, phase transformations drive
microscopic plasticity that, in part, determines the residual
stresses and distortion that result. In order to develop an accurate
numerical simulation capability for carburization and quenching,
one must take care to properly account for the coupling between
the thermal, mechanical, and microstructural physical mechanisms
at work.
The modeling strategy adopted here couples differential equations for phase evolution with a multiphase internal state variable
material model. The kinetic rate equations for each product phase
are derived using a thermodynamic formulation and fit to experimental data. The kinetics model is validated using time temperature transformation TTT data, continuous cooling transformation
CCT data, and by studying the influence of stress on the kinetics
through compression and tension experiments. The elastic-plastic
were partially successful in the thick strip limit, but suffered from
a lack of quantitatively reliable constitutive data. In particular,
data available for rate-independent yield strength, recovery at
large strain and directional hardening have been insufficient to
accurately account for low temperature behavior and load reversals. The computational predictions of Henriksen et al. 4 also
illustrated a significant sensitivity to both phase transformation
kinetics and the flexural rigidity of the thin strips. They correctly
focused attention on the five constitutive parameters most influential in analysis of quenched specimens: the elastic moduli, yield
strength, hardening moduli, thermal expansion and phase transformation volume change. While they relied predominantly on literature data, the work presented here draws on data collected from an
expansive test series on low carbon steels 1.
Empirical methods for incorporating a temperature dependent
yield strength to simulate a phase change do not account for the
volume change or any additional plasticity 6,7. Mimicking the
phase change with large changes in the thermal expansion coefficient can capture the effects of the spherical volume change, but
not the microplasticity that accompanies them 6,8,9. Calculations that account for the dilatational volume change explicitly,
but not the accompanying microscopic deviatoric TRIP strains
exhibit discrepancies with measured residual stresses 10,11. For
problems that are predominantly deformation driven or exhibit
large kinematic constraints, the predicted stresses can be substantially in error. Simulations with and without this augmented plasticity indicate that neglecting this strain contribution can result in
residual stresses that are incorrect in sign and magnitude
6,12,13. Because transformation strains are accounted for locally, their effect on global distortions and residual stresses will,
in general, be problem dependent 8,12.
Finally, while previous empirical models for phase transformation kinetics have proven their utility for reconstructing CCT and
TTT curves, a rate formulation capable of recovering smooth
transformation rates and accurate volume fraction time histories is
required to construct a robust numerical tool for multiphase
behavior.
Physical Mechanisms
Distortion and residual stresses can result from carburizing and
quenching alloy steel components. Both are caused by internal
loading from strains that evolve as a consequence of interstitial
lattice accommodation, cooling and phase transformation-induced
dilatation. In many cases and especially at high temperature, internal stresses are sufficient to exceed the local yield strength.
This gives rise to path dependent plastic flow. The levels of stress
are determined primarily by the timing of phase transformation
strains relative to the thermal contraction and the degree to which
these dilatations are suppressed by the surrounding material.
The carburizing process is performed at high temperature where
the diffusivity of carbon in steel is high. Upon brief exposure to a
carbon-rich atmosphere, carbon diffuses into the alloy lattice interstitial sites expanding the lattice and introducing a carbon gradient through the strip thickness. The carbon rich surface is
harder, more wear resistant and, upon quenching, results in a localized compressive residual stress state that strengthens the part
against imposed tensile stresses that accompany sustained fatigue
loading.
At cooling rates specified in the quench history, time scales are
too small for carbon diffusion to take place and austenite transforms via a shear mechanism to a body centered tetragonal structure known as martensite. This athermal transformation induces a
volumetric expansion because the lattice volume of the martensite
is larger than that of the austenite from which it formed. Further,
higher carbon contents reduce the temperature at which the martensite first forms and result in a larger volume change. The net
deflections of the carburized strip result from a series of competing strains imposed by the evolving microstructure.
First, the strip is uniformly heated and carburized resulting in
thermal expansion locally augmented by interstitial accommodation of carbon in the lattice. This results in an initial convex deflection of the strip due to carburization. Upon cooling, the low
carbon side of the strip reaches its transformation temperature
first. Martensite forming on this back side imposes a dilatational
strain that bends the strip back. Once the lower start temperature
of the carbon rich surface is reached, a larger dilatational strain
accompanying the transformation of high carbon martensite
changes the sense of deflection once more.
This series of alternating flexures results in a net convex distortion of the carburized surface and imbedded compressive residual
stresses at both surfaces. The experimental arc deflections reported by Larson 5 are illustrated in Fig. 2. The amplitude of the
arc deflections and severity of residual stress profiles are the result
of a complex path-dependent deformation history resulting from
thermal and phase transformation dilatational strains that are functions of the cooling and deformation rates, temperature and carbon
content.
APRIL 2003, Vol. 125 117
Fig. 2 Distortion of Almen strip set as a function of strip thickness from 5. The top convex surface of the
strip is the carburized surface.
Model Formulation
The modified Almen samples were subjected to a heat treat
schedule composed of furnace carburizing followed by oil and air
quenches, respectively. The process schedule is specified by the
temperature history pictured in Fig. 3 reproduced from Larson
5. The strip is carburized in a three step furnace hold, quenched
in oil, and, finally, air cooled to room temperature. The heat treat
process is broken down into a series of three uncoupled analyses:
carburization, thermal analysis and structural analysis. The interaction of the three modules is schematically represented in Fig. 4.
A diffusion-based carburization analysis is performed by applying a specified carbon potential to one side of the strip. This carburization process is performed at high temperature 900C
where the diffusivity of carbon in steel is high. Carbon diffuses
into interstitial sites expanding the lattice and introducing a car-
i i W ei i i W ei 2 De i
Fig. 3 Heat treatment schedule for the experimental Almen
samples
(1)
Fig. 4 Uncoupled analyses available within the NCMS heat treatment process model
(2)
(3)
(4)
The plastic flow rule is chosen to have a strong nonlinear dependence upon the effective stress
Dpi f i sinh
i Y i
V i
i i
,
i i
(5)
(6)
i D pi , V i sinh1
D pi
f i
(7)
C3
1tanh C 19 C 20 exp C 4 /
2
f i C 5 exp C 6 /
(8)
(9)
(10)
(12)
R s( i ) ( )
and
describe the diffusionThe scalar functions
controlled static or thermal recovery, while r (di ) ( ) and R (di ) ( ) are
scalar functions describing dynamic recovery. The anisotropic
hardening modulus is h ( i ) ( ), and the isotropic hardening modulus is H ( i ) ( ). The temperature dependent hardening and recovery
parameters are given as
r di C 7 exp C 8 /
(13)
h i C 9 C 10
(14)
r si C 11 exp C 12 /
(15)
R di C 13 exp C 14 /
(16)
H C 15C 16
(17)
R si C 17 exp C 18 / .
(18)
Transformation Plasticity
For multiphase materials, the effects of phase transformation
induced plastic strain must be included. When steel alloys are
cooled from above the austenization temperature, a solid state
phase transformation occurs, resulting in product phases that are
larger in volume and harder than the surrounding parent phase.
This volume difference between the crystal structures causes microscopic plastic flow as the transformation proceeds. In the presence of a deviatoric stress field the straining from the volume
misfit exhibits a deviatoric part proportional to the surrounding
stress. Since the product phases are generally stronger, this results
in an internal stress in the austenite. In this pre-loaded state, the
multiphase composite can yield when the applied stress is less
than the yield strength of the virgin austenite. Thus, the multiphase steel exhibits an apparent softening during phase transformation. Accounting for the resulting inelastic straining in the flow
rule provides a natural way to model the multiphase yield drop
and additional plasticity characteristic of transforming alloys.
Leblond et al. 17,18 have outlined an extensive theoretical
treatment of transformation plasticity. Leblond et al. 19,20 further provided a mathematical overview wherein the transformation plastic strain rate is given by
TRI P
K V
y V
(19)
E M E A
ij
1E A
(20)
where
E M M 0 M 1 M 2 2 M 3 3
(21)
(22)
is the corresponding temperature dependence in the austenite. Figure 7 illustrates the extensional strain produced in dilatometer
specimens by thermal contraction and martensitic phase transformation as a function of temperature and carbon content. The deviation of each curve from the linear thermal contraction is precisely the transformation strain given in Eq. 18. The coefficients
appearing in Eqs. 21 and 22 are carbon-dependent as well.
This carbon dependence is illustrated for martensite in Fig. 8 for a
series of discrete temperatures.
We propose a new form for the deviatoric TRIP strain rate
motivated by limit behaviors of the Weibull probability distribution function
P
D TRI
Am
B B
m1
exp
(23)
(24)
1.
i
(25)
We presume that athermal transitions are a special case of isothermal kinetics in which the mobility function approaches infinity. This implies that, for martensite formation isothermal martensite is not considered here, a time-dependent kinetic equation
is not necessary since equilibrium is always attained instantaneously upon changing the temperature. Figure 10 illustrates this
idea through a plot of free energy versus temperature. The energy
minimum corresponds to the equilibrium volume fraction of martensite. As temperature decreases during quenching, this minimum
shifts to higher martensite volume fractions. Experimental curves
depicting martensite volume fraction as a function of temperature
can therefore be interpreted as a description of the minimum value
of a temperature dependent energy function.
The most commonly used description of such well states is the
Koistinen-Marburger equation 21,
APRIL 2003, Vol. 125 121
Fig. 12 Comparison of experimental data with the new kinetics DANTE model prediction and the prediction of the
Koistinen-Marburger K-M equation
Fig. 10 Schematic indicating the shifting of the equilibrium
volume fraction of martensite as a function of temperature
1exp b M S U M S ,
(26)
M S
U M S 0,
M S
M S
U M S ,
M S M F
d
d
M C C 1 C U M S
dt
dt
(27)
(28)
where
C 0 1C
C 0 1C
(30)
M C 0 1 C 2 C 2 3 C 3
and C is the carbon content. This equation represents a differential
relationship between martensite volume fraction and temperature,
but it is cast in a time-rate form so that it can be solved incrementally with the thermal simulation. The Koistinen-Marburger equation is recovered as a special case when 0, 1, and b.
The best match with dilatometry experiments was obtained using the Andrews nonlinear equation for the martensite start temperature, M S 25:
M S C 512453C16.9Ni9.5M o217C 2 71.5 C M n
15Cr67.6 C Cr 10Co7.5Si
(29)
(31)
Fig. 13 Almen strip carbon profile with depth from the carburized surface for h 1.30 mm
Fig. 14 Almen strip carbon profile with depth from the carburized surface for h 3.18 mm
Here the alloying elements are given in weight per cent. There are
three additional functions that need to be fitted, , and . As
indicated above, each of these functions is assumed to be a polynomial function of carbon level. A differential fitting routine was
developed to obtain the optimum values of these parameters for
low carbon alloys.
This model was used to generate the martensite volume fraction
thermal histories shown in Fig. 11. Note that the dilatometry data
was used to fit the kinetics model, so the results shown are not so
much a prediction of the model as much as a demonstration that
the model can capture the desired kinetic behavior. Figure 12
compares the predicted martensite volume fraction curve predicted by the new kinetics model with a similar prediction using
the Koistinen-Marburger equation. Note the burst-type behavior
predicted by the Koistinen-Marburger equation at the onset of the
transformation. This abrupt phase change behavior is not observed
experimentally.
References
1 Predictive Model & Methodology for Heat Treatment Distortion, 1997
Phase I Project Summary Report, Constitutive Model Task Team; NCMS
Project, January 1994 December 1997.
2 Lusk, M., Krauss, G., and Jou, H.-J., 1995, A Balance Principle Approach for
Modeling Phase Transformation Kinetics, Journal de Physique IV, C8, pp.
279284.
3 ABAQUS Users Manual V5.8, 1998, Hibbitt, Karlsson and Sorensen Pawtucket, RI.
4 Henriksen, M., Larson, D. B., and Van Tyne, C. J., 1992, On the Analysis of
Distortion and Residual Stress in Carburized Steels, ASME J. Eng. Mater.
Technol., 114, pp. 362367.
5 Larson, D., 1990, Finite Element Analysis of Residual Stress and Distortion
in Forged and Carburized Gear Steel, M.S. thesis T-3932, Colorado School of
Mines, Golden, CO.
6 Goldak, J. A., 1990, Modeling Thermal Stresses and Distortions in Welds,
Recent Trends in Welding Science and Technology, S. A. David and M. Vitek,
eds., ASM International, Gatlinburg, TN, pp. 71 82.
7 Dubois, D., Devaux, J., and Leblond, J. B., 1984, Numerical Simulation of a
Welding Operation: Calculation of Residual Stresses and Hydrogen Diffusion, Proceedings of the 5th International Conference on Pressure Vessel
Technology, 2, American Society of Mechanical Engineers, New York, pp.
12101239.
8 Sjostrom, S., 1985, Interactions and Constitutive Models for Calculating
Quench Stresses in Steel, Mater. Sci. Technol., 1, pp. 823 829.
9 Goldak, J. A., 1986, Computational Weld Mechanics, Proceedings of the
International Symposium on Computer Modeling of Fabrication Processes and
Constitutive Behavior of Metals, Ottawa, Canada.
10 Oddy, A. S., Goldak, J. A., and McDill, J. M. J., 1992, Transformation Plasticity and Residual Stresses in Single-Pass Repair Welds, ASME J. Pressure
Vessel Technol., 114, pp. 3338.
11 Josefson, B. L., and Karlsson, C. T., 1992, Transformation Plasticity Effects
on Residual Stresses in a Butt-Welded Pipe, ASME J. Pressure Vessel Technol., 114, pp. 376 378.
12 Oddy, A. S., Goldak, J. A., and McDill, J. M. J., 1990, Numerical Analysis of
Transformation Plasticity in 3D Finite Element Analysis of Welds, Eur. J.
Mech. A/Solids, 93, pp. 253263.
13 Goldak, J. A., 1991, Coupling Heat Transfer, Microstructure Evolution and
Thermal Stress Analysis in Weld Mechanics, Proceedings of the IUTAM Symposium, Lulea, Sweden, 131.
14 Bammann, D. J., Chiesa, M. L., and Johnson, G. C., 1996, Modeling Large
Deformation and Failure in Manufacturing Processes, in Proceedings of the
19th International Congress of Theoretical and Applied Mechanics, Tatsumi,
Wannabe and Kambe, eds., Kyoto, Japan, pp. 359376.
15 Bammann, D. J., and Ortega, A. R., 1993, The Influence of the Bauschinger
Effect and Yield Definition on the Modeling of Welding Processes, Welding
and Advanced Solidification Processes-VI, T. S. Piwonka, V. Voller, and L.
Katgerman, eds., The Minerals, Metals & Materials Society, Warrendale, PA,
pp. 543551.
16 Lathrop, J. F., 1997, BFITA Program to Analyze and Fit the Sandia Plasticity BAMMANN Model Parameters to Experimental Data, SAND978218.
17 Leblond, J. B., Mottet, G., and Devaux, J. C., 1986, A Theoretical and Numerical Approach to the Plastic Behavior of Steels During Phase Transformations: IDerivation of General Relations, J. Mech. Phys. Solids, 344, pp.
395 409.
18 Leblond, J. B., Mottet, G., and Devaux, J. C., 1986, A Theoretical and Numerical Approach to the Plastic Behavior of Steels During Phase Transformations: IIStudy of Classical Plasticity for Ideal-Plastic Phases, J. Mech.
Phys. Solids, 344, pp. 411 432.
19 Leblond, J. B., Devaux, J., and Devaux, J. C., 1989, Mathematical Modeling
of Transformation Plasticity in Steels I: Case of Ideal-Plastic Phases, Int. J.
Plast., 5, pp. 551572.
20 Leblond, J. B., Devaux, J., and Devaux, J. C., 1989, Mathematical Modeling
of Transformation Plasticity in Steels II: Coupling With Strain Hardening Phenomena, Int. J. Plast., 5, pp. 573591.
21 Koistinen, D., and Marburger, R., 1959, Acta Metall., 7, p. 59.
22 Skrotzki, B., 1991, J. de Physique IV Colloque, C81, p. 367.
23 Grange, R., and Stewart, H., 1946, Trans. AIME, 167, p. 467.
24 Bammann, D., Prantil, V., Kumar, A., Lathrop, J., Mosher, D., Lusk, M., Jou,
H.-J., Krauss, G., Elliott, W., 1996, Proceedings of the 2nd International Conference on Quenching and the Control of Distortion, G. Totten, M. Howes, S.
Sjostrom, and K. Funatani, eds., ASM, p. 367.
25 Andrews, K. W., 1965, Empirical Formulae for the Calculation of Some
Transformation Temperatures, J. Iron Steel Inst., London, pp. 721727.