Bounding the plastic strength of polycrystalline solids by linear-comparison homogenization methods
Martn I. Idiart
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BY MARTN I. IDIART1,2,*
The elastoplastic response of polycrystalline metals and minerals above their brittle
ductile transition temperature is idealized here as rigidperfectly plastic. Bounds on the
overall plastic strength of polycrystalline solids with prescribed microstructural statistics
and single-crystal plastic strength are computed by means of a linear-comparison
homogenization method recently developed by Idiart & Ponte Castaeda (Idiart & Ponte
Castaeda 2007 Proc. R. Soc. A 463, 907924 (doi:10.1098/rspa.2006.1797)). Hashin
Shtrikman and self-consistent results are reported for cubic and hexagonal polycrystals
with varying degrees of crystal anisotropy. Improvements over earlier linear-comparison
bounds are found to be modest for high-symmetry materials but become appreciable for
low-symmetry materials. The largest improvement is observed in self-consistent results
for low-symmetry hexagonal polycrystals, exceeding 15 per cent in some cases. In addition
to providing the sharpest bounds available to date, these results serve to evaluate the
performance of the aforementioned linear-comparison method in the context of realistic
material systems.
1. Motivation
The elastoplastic response of polycrystalline metals and minerals above their
brittleductile transition temperature is to a great extent dictated by the
morphology, lattice orientation and elastoplastic response of each individual
single-crystal grain composing the aggregate. Relating the macroscopic response
with the microscopic properties is necessary to estimate the deformation-induced
plastic anisotropy that develops in these materials when subjected to large
deformations, a problem relevant to various engineering applications such as
metal-forming processessee the monograph by Kocks et al. (1998). Very often
the response of these materials is idealized as elastically rigid and plastically
Bounding the plastic strength
non-hardening. Within this the so-called rigidperfectly plastic model, the above
problem reduces to finding the macroscopic yield surface of the polycrystal
given the yield surface at the single-crystal level and the statistics of the
morphology and orientation distributions of the grains. Owing to their inherent
microstructural randomness, cognate polycrystalline solids do not exhibit a single
response but ahopefully narrowrange of responses. Therefore, one can either
develop estimates that yield a single representative response or derive bounds
for the entire range of possible responses. This work is concerned with bounds.
Bounds are also useful for two additional reasons: they provide benchmarks to
test estimates and they can be used as estimates themselves.
The simplest bounds for the yield surface of polycrystalline solids are the outer
bound of Taylor (1938) and the inner bound of Reuss (1929). Their extremal
character was proved by Bishop & Hill (1951). These elementary bounds are
obtained by assuming uniform strain-rate and uniform stress fields in the classical
minimum energy principles, and make use of one-point microstructural statistics
only. They have proved useful in the context of high-symmetry polycrystalline
solidslike face-centred cubic solidswhere the heterogeneity contrast is low,
but as crystal anisotropy increases their predictions diverge and become highly
inaccurate. This fact has motivated the development of refined bounds that
can incorporate higher order microstructural statistics. Most of those bounds
have been derived in the context of nonlinear viscoplasticity, which includes
rigid-perfect plasticity as a limiting case. The first bounds for polycrystalline
solids that account for two-point statistics were derived by Dendievel et al.
(1991) via the nonlinear HashinShtrikman procedure initially proposed by Willis
(1983) and developed further by Talbot & Willis (1985). A more general method
inspired by the linear-comparison procedure of Ponte Castaeda (1991) was later
proposed by deBotton & Ponte Castaeda (1995) and developed further by Ponte
Castaeda & Suquet (1998). This linear-comparison method allows the use of any
available bound for linearly elastic polycrystals to produce bounds for nonlinear
viscoplastic polycrystals, thus having the potential of incorporating higher order
statistics. The optimal linearization is obtained via suitably designed variational
principles. This linear-comparison method was applied to cubic and hexagonal
polycrystals by Nebozhyn et al. (2000, 2001) and Liu & Ponte Castaeda (2004),
who showed that the linear-comparison predictions for rigidperfectly plastic
polycrystals improve significantly over the elementary predictions of Taylor and
Reuss, especially when crystal anisotropy is large. In addition, their results served
to demonstrate the inconsistency of an incremental theory of polycrystalline
plasticity proposed by Hill (1965) and Hutchinson (1976), which was found to
violate the bounds. More recently, Lebensohn et al. (2011) have reported
linearcomparison bounds for (two-phase) voided polycrystals and have shown that
tangent theories of polycrystalline plasticity such as those proposed by Molinari
et al. (1987), Lebensohn & Tom (1993) and Bornert et al. (2001) can also
violate bounds.
Idiart & Ponte Castaeda (2007a) have recently shown that the
linearcomparison methods of deBotton & Ponte Castaeda (1995) and Ponte
Castaeda & Suquet (1998) make implicit use of a relaxation in their linearization
scheme which weakens the resulting bounds. Eliminating this relaxation leads
to sharper bounds but increases the computational complexity. Idiart & Ponte
Castaeda (2007a,b) derived non-relaxed linear-comparison bounds and applied
them to a model material consisting of a porous single crystal with cylindrical
symmetry under anti-plane loading. They found that the improvement over the
relaxed bounds increased with increasing number of crystal slip systems, being as
much as 10 per cent in some extreme cases. Motivated by these developments, the
method of Idiart & Ponte Castaeda (2007a) is used in this work to bound the
plastic strength of a fairly general class of polycrystalline solids made of cubic and
hexagonal single crystals with varying degrees of plastic anisotropy. In addition
to providing the sharpest bounds available to date for polycrystalline plastic
solids, these results are used to evaluate the performance of the non-relaxed
linear-comparison method in the context of realistic material systems.
2. The polycrystalline solid model
Polycrystals are idealized here as random aggregates of perfectly bonded single
crystals (i.e. grains). Individual grains are (...truncated)