Abstract
In this paper, we formulate a theory for the coupling of accretion mechanics and thermoelasticity. We present an analytical formulation of the thermoelastic accretion of an infinite cylinder and of a two-dimensional block. We develop numerical schemes for the solution of these two problems, and numerically calculate residual stresses and observe a strong dependence of the final mechanical state on the parameters of the accretion process. This suggests the possibility to predict and control thermal accretion processes of soft materials by manipulating thermal parameters, and therefore, to realize additively manufactured soft objects with the desired characteristics and performances.
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Notes
We denote by \({\varvec{T}}^{\star }\) the dual of the \((^1_1)\)-rank tensor \({\varvec{T}}\,\): operating on a 1-form \(\varvec{\lambda }\), it contracts its upper index with \(\varvec{\lambda }\), i.e., \({\varvec{T}}^{\star } \varvec{\lambda }=T^B{}_A\lambda _B{{\mathrm {d}}} X^A\). It should not be confused with the adjoint operator \({}^{{\mathsf {T}}}\), cf. footnote 3.
Rank-1 convexity allowed Sozio and Yavari [49] to use an energetic argument to show that the absence of in-layer deformation and the vanishing of out-of-layer stress (tractions) imply \(\bar{{\varvec{F}}}={\varvec{Q}}\). Note that being an isometry, the accretion tensor \({\varvec{Q}}\) represents an undeformed state.
We denote the adjoint of \({\varvec{F}}\) by \({\varvec{F}}^{{\mathsf {T}}}\) and it is defined such that \({\varvec{g}}({\varvec{F}}{\varvec{W}},{\varvec{w}})={\varvec{G}}({\varvec{W}},{\varvec{F}}^{{\mathsf {T}}}{\varvec{w}})\) for any pair \(({\varvec{W}},{\varvec{w}})\in T_X{\mathcal {B}}_t\times T_{\varphi _t(X)}{\mathcal {S}}\). In components, \((F^{{\mathsf {T}}})^A{}_a=g_{ab}F^b{}_BG^{AB}\).
In Appendix D we discuss the derivation of this inequality.
Note that \({\varvec{G}}^{\sharp } {\mathrm {dT}} = {\text {Grad}}T\).
There are many other choices that will result in the same stress calculation. As a matter of fact, for isotropic solids the geometric theory suggests that the material body is represented by a class of infinitely many isometric Riemannian manifolds. The anisotropic case is slightly more complicated as one needs to look at the symmetry group for the constitutive equation, but there is still some arbitrariness. This was discussed in detail in [48, 50].
If the inner boundary is subject to a traction (pressure) \(p_i\), the condition \(\sigma ^{rr}(S(t),t)=-p_i(t)\) gives the following equation
$$\begin{aligned} \int \limits _{R_i}^{S(t)} \frac{\mu (T(\xi ,t))}{{\bar{r}}(\xi )} \left[ 1-\frac{{\bar{r}}^4(\xi ) e^{4\omega (T(\xi ,t))} }{r^4(\xi ,t) }\right] {{\mathrm {d}}}\xi = p_i(t). \end{aligned}$$(34)Note that \(\sigma ^{\theta \theta }(S(t),t)=0\) is not assumed; it is anticipated by virtue of \({\varvec{Q}} = \bar{{\varvec{F}}}\).
It is assumed that throughout the whole accretion process the configuration of the accretion surface is given by points (x, f(x, t) ), for some time-dependent f, so that the vertical addition of material on the whole upper boundary will always be possible.
Unlike the one-dimensional example of the axi-symmetric infinite cylinder, it is not possible to define s(t) as the deformation is not uniform along the width of the block.
AY is grateful to Prof. Marshall Slemrod for a discussion that helped us find and correct this mistake.
These simple relations were written incorrectly in Eq. (62) of [43].
Note that in addition to the last two relations in Eq. (62), Eq. (66) in [43] is incorrect as well, and the final form of the energy balance in Eq. (69) must be changed to read \(\rho T\dot{{\mathcal {N}}}=\rho R-{\text {Div}}{\varvec{H}}+\rho T\frac{\partial {\mathcal {N}}}{\partial {\mathbf {G}}}\!:\!\dot{{\mathbf {G}}}\). Fortunately, nothing else in [43] was affected by this mistake.
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Acknowledgements
This research was supported by NSF-Grant Nos. CMMI 1130856 and ARO W911NF-18-1-0003.
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Appendices
A A nonlinear thermoelastic constitutive model
In this appendix, we present a thermoelastic model following the works of Chadwick [3], Ogden [37,38,39], and Holzapfel and Simo [24]. See [43] for more details. For a homogeneous isotropic solid, we denote by \(\kappa _0\), \(\mu _0\) and \(\beta _0\), the bulk modulus, the shear modulus, and the volumetric coefficient of thermal expansion at \(T_0\), respectively, with \(\beta (X,T) = \frac{\partial }{\partial T}{\text {tr}} \varvec{\omega }(X,T)\), while in the isotropic case \(\beta (X,T) = 3\frac{\partial }{\partial T}\omega (X,T) = 3 \alpha (X,T)\) in 3D, and \(\beta (X,T) = 2\frac{\partial }{\partial T}\omega (X,T) = 2 \alpha (X,T)\) in 2D. We consider the following constitutive model
where \(\tilde{I}=J^{-2/3}I\), \(I={\text {tr}}{\varvec{C}}\), \({J} = \sqrt{\det {\varvec{C}}}\), and \(c_E\) is the specific heat capacity at constant strain. In the incompressible case, we have the constraint \(J=1\) associated with the pressure field p as the Lagrange multiplier and the constitutive model transforms to read
plus the Lagrange multiplier part \(p(J-1)^2\). Note that the shear modulus is linear in temperature, i.e.,
The simplest thermoelastic model for the expansion coefficients is given by a constant \(\alpha \), viz.
B A remark on the material metric
Equation (2) is a generalization of the isotropic case that appeared in [40]. In section 2.1 of [43], due to a mis-manipulation of the musical operators for raising and lowering indices, the representation of the material metric using the \(({}^{1}_{1})\)-tensor \(\varvec{\omega }\) was mistakenly presented as
Indeed, this representation may violate the symmetry requirement for the Riemannian metric \({\varvec{G}}\), while the representation (2) ensures its symmetry. In what follow, we provide a correction of the proof appearing in section 2.1 of [43]. The manifold \(({\mathcal {B}},{\varvec{G}}_0)\)—which corresponds to the stress-free temperature field \(T_0=T_0(X)\)—is flat. Hence, there exists a local coordinate chart \(\{Y^A\}\) in which
Following Ozakin and Yavari [40], the temperature-dependent material metric can be written as
where \(\{\omega _{A}\}_{A=1,2,3}\) describes the thermal expansion properties of the material such that \(\omega _K\) is related to the thermal expansion coefficient \(\alpha _K\) in the direction \(\frac{\partial }{\partial Y^K}\) by
and \(\omega _K(X,T_0)=0\). Let the change of basis between \(\{Y^A\}_{A=1,2,3}\) and some arbitrary local coordinate chart \(\{X^A\}_{A=1,2,3}\) be written as
which also reads as
Then it follows that
Let \(\varvec{\omega }\) be the \(({}^{1}_{1})\)-tensor
However, in \(\{ X^A\}\), one has
Hence, the material metric transforms to
where \((G_0)_{LM}\) are the components of \({\varvec{G}}_0\) in \(\{ X^A\}\). This is the coordinate representation of (2). Note that even though the general representation for the material metric used in [43] had this symmetry fallacy, the results of the paper and the examples were not affected and remain valid.
C Christoffel symbols for the accreting cylinder
First note that denoting with \((\Gamma _0)^A{}_{BC}\) the Christoffel symbols relative to \({\varvec{G}}_0\) as in (6), one obtains
Therefore, as \({\varvec{G}}_0^{\sharp }:{\varvec{G}}_0={\text {dim}}{\mathcal {B}}\), one has
Under the assumption of a uniform material one has \(\omega _{,C} = \frac{\partial \omega }{\partial T} \,T_{,C} = \alpha \,T_{,C}\), i.e., \({\mathrm {d}}\omega = \alpha \,{\mathrm {d}}T\), so one writes
Now we compute the Christoffel symbols for the material metric \({\varvec{G}}\) of (25). The only nonzero Christoffel symbols are
Now one can compute the material divergence \({\text {Div}}[K(T) {\varvec{G}}^\sharp {\mathrm {dT}}]\) for the heat equation as
D The reduced form of the Clausius–Duhem inequality in thermoelastic accretion
In this appendix, we discuss the restrictions that the second law of thermodynamics imposes on constitutive equations. In particular, we correct a mistake in [43],Footnote 11 which fortunately did not affect any of the results or conclusions of that work. The localized form of the Clausius-Duhem inequality reads
where \({\mathcal {N}}={\mathcal {N}}(X,T,{\varvec{C}}^\flat ,{\varvec{G}})\) is the specific entropy. Expanding Eq. (70) and multiplying by \(T>0\) one obtains
where in a local coordinate chart \(\{X^A\}\), the 1-form \({\mathrm {d}}T\) has the representation \({\mathrm {d}}T=\frac{\partial T}{\partial X^A}dX^A\). The specific free energy function has the form \(\Psi =\Psi (X,T,{\varvec{C}}^\flat ,{\varvec{G}})\). The internal energy is defined as the Legendre transform of the free energy with respect to the conjugate variables T and \({\mathcal {N}}\), i.e., \({\mathcal {E}}=T{\mathcal {N}}+\Psi \), and hence, \({\mathcal {E}}={\mathcal {E}}(X,{\mathcal {N}},{\varvec{C}}^\flat ,{\varvec{G}})\,\). ThereforeFootnote 12
The localized balance of energy reads [43]
This can be rewritten in terms of the specific entropy as
Substituting (74) into (71) one obtains
This inequality must hold for all deformations \(\varphi \) and metrics \({\varvec{G}}\,\). ThereforeFootnote 13
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Sozio, F., Faghih Shojaei, M., Sadik, S. et al. Nonlinear mechanics of thermoelastic accretion. Z. Angew. Math. Phys. 71, 87 (2020). https://doi.org/10.1007/s00033-020-01309-5
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DOI: https://doi.org/10.1007/s00033-020-01309-5