Abstract
We address the fundamental difference between solid-solid and liquid-liquid phase transitions within the Ericksen’s nonlinear elasticity paradigm. To highlight ideas, we consider the simplest nontrivial 2D problem and work with a prototypical two-phase Hadamard material which allows one to weaken the rigidity and explore the nature of solid-solid phase transitions in a “near-liquid” limit. In the language of calculus of variations we probe limits of quasiconvexity in an “almost liquid” solid by comparing the thresholds for cooperative (laminate based) and non-cooperative (inclusion based) nucleation. Using these two types of nucleation tests we obtain for our model material surprisingly tight two-sided bounds on the elastic binodal without directly computing the quasiconvex envelope.
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Notes
In principle, our methodology is also applicable in 3D. In this paper we have chosen a 2D setting to make the ideas and techniques fully transparent and to be able to illustrate them graphically.
Formula (3.2) only needs to hold in an arbitrary neighborhood of \([d_{1},d_{2}]\). The potential \(h(d)\) can be modified outside of that neighborhood arbitrarily, as long as \(h^{**}(d)=h(d)\) there. In particular, the singular behavior of \(h(d)\) as \(d\to 0^{+}\), required in nonlinear elasticity, can be easily assured.
We use the notation ± to make two statements at the same time, one for the “+” sign, the other for the “−” sign. For example, our statement says that the matrix \(\boldsymbol{F}_{+}\) has two singular values \(\varepsilon _{0}\) and \(\varepsilon _{+}\) and the matrix \(\boldsymbol{F}_{-}\) has two singular values \(\varepsilon _{0}\) and \(\varepsilon _{-}\).
Technically, at the W-points there could be other, not necessarily diagonal critical states, however, by continuity, the diagonal critical points would still deliver the global minimum of \(\Psi (\boldsymbol{F})\).
This inequality is equivalent to \(|\mathrm {dev}(\boldsymbol{H})|^{2}\ge 0\), where \(2\mathrm {dev}(\boldsymbol{H})=\boldsymbol{H}+\boldsymbol{H}^{T}-(\mathrm {Tr}\,\boldsymbol{H})\boldsymbol{I}_{2}\).
We can assume. without loss of generality, that \(h(d)\ge 0\) and \(h(d)=0\) only at \(d=d_{1}\) and \(d=d_{2}\).
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YG was supported by the National Science Foundation under Grant No. DMS-2005538. The work of LT was supported by the French grant ANR-10-IDEX-0001-02 PSL.
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Appendix: Calculation of the Jump Set for Hadamard Materials
Appendix: Calculation of the Jump Set for Hadamard Materials
Here we recall the calculation of the jump set from [27] for energies (3.1).
We start with the first equation in (2.3) expressing the kinematic compatibility of the deformation gradients \(\boldsymbol{F}_{+}\) and \(\boldsymbol{F}_{-}\). Taking the determinant of both sides we obtain
Using the formula
for the Piola–Kirchhoff stress we compute
where we have used the well-known relation \(\mathrm {cof}(\boldsymbol{F}_{-}+\boldsymbol{a}\otimes \boldsymbol{n})\boldsymbol{n}=(\mathrm {cof}\boldsymbol{F}_{-})\boldsymbol{n}\). Similarly,
Thus, the second and the third equations in (2.3) become
where \(\boldsymbol{C}_{\pm}=\boldsymbol{F}_{\pm}^{T}\boldsymbol{F}_{\pm}\) is the Cauchy–Green strain tensor. We conclude that \(\boldsymbol{n}\) must be an eigenvector of \(\boldsymbol{C}_{-}\). Equations (A.2) permit us to find a relation between the two Cauchy–Green tensors \(\boldsymbol{C}_{\pm}\). Using the kinematic compatibility equation (2.3)1 we compute
Applying \(\boldsymbol{F}_{-}^{T}\) to the first equation in (A.2) we obtain \(\boldsymbol{F}_{-}^{T}\boldsymbol{a}=-(\lbrack \!\lbrack h' \rbrack \!\rbrack /\mu )d_{-}\boldsymbol{n}\), so that
It follows that the Cauchy–Green tensors \(\boldsymbol{C}_{+}\) and \(\boldsymbol{C}_{-}\) are simultaneously diagonalizable, since, by (A.2) \(\boldsymbol{n}\) is an eigenvector of \(\boldsymbol{C}_{-}\). According to equation (A.3) symmetric matrices \(\boldsymbol{C}_{+}\) and \(\boldsymbol{C}_{-}\) have the same pair of mutually orthogonal eigenvectors \(\boldsymbol{n}\) and \(\boldsymbol{n}^{\perp}\) with the same eigenvalues corresponding to \(\boldsymbol{n}^{\perp}\). Hence, singular values of \(\boldsymbol{F}_{\pm}\) would be \((\varepsilon _{\pm}, \varepsilon _{0})\), the first one corresponding to the eigenvector \(\boldsymbol{n}\) of \(\boldsymbol{C}_{\pm}\). Substituting the first equation in (A.2) into (A.1) we obtain
which can be written in the more symmetric form as
This will be the equation for the jump set, when we determine \(d_{+}\) as a function of \(d_{-}\) from the Maxwell relation (the last equation in (2.3), which hasn’t been used so far). It is well-known that the Maxwell relation does not change if we add any quadratic function of \(\boldsymbol{F}\) to the energy. Thus, the term \(\mu |\boldsymbol{F}|^{2}/2\) can be disregarded and the Maxwell relation becomes
Recalling that due to (A.1) \((\mathrm {cof}\boldsymbol{F}_{+})\boldsymbol{n}\cdot \boldsymbol{a}=(\mathrm {cof}\boldsymbol{F}_{-})\boldsymbol{n}\cdot \boldsymbol{a}=\lbrack \!\lbrack d \rbrack \!\rbrack \) we obtain
Equation (A.5) has a geometric meaning. It says that the secant line joining \((d_{-},h'(d_{-}))\) and \((d_{-},h'(d_{-}))\) together with the graph of \(h'(d)\) bound two regions of equal areas. For a double-well shaped potential \(h(d)\) there exists a single interval \((d_{1},d_{2})\) on which \(h(d)\) differs from its convex hull, which on \((d_{1},d_{2})\) agrees with the common tangent line at \(d_{1}\) and \(d_{2}\) to the graph of \(h(d)\). In terms of \(h'(d)\) this double-tangency can also be interpreted geometrically as the horizontal “Maxwell line” with the equal area property. In that case there exist \(d_{0}\in (d_{1},d_{2})\), such that for any \(d_{-}\in (d_{1},d_{0})\) there is a unique \(d_{+}\in (d_{0},d_{2})\) satisfying (A.5). In other words, for every \(d_{-}\in (d_{1},d_{0})\) there is a unique \(d_{+}=D(d_{-})\) with equal area property. (By continuity we can set \(D(d_{0})=d_{0}\).) Regarding the function \(D(d)\) as known, equation (A.4) provides the explicit description of the jump set in terms of the singular values of \(\boldsymbol{F}_{\pm}\).
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Grabovsky, Y., Truskinovsky, L. Solid Phase Transitions in the Liquid Limit. J Elast (2023). https://doi.org/10.1007/s10659-023-10022-z
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DOI: https://doi.org/10.1007/s10659-023-10022-z