Abstract
An exploration of representations of free energies and associated rates of dissipation for a broad class of nonlinear viscoelastic materials is presented in this work. Also included are expressions for the stress functions and work functions derivable from such free energies. For simplicity, only the scalar case is considered. Certain standard formulae are generalized to include higher power terms.
It is shown that the correct initial procedure in this context is to specify the rate of dissipation as a positive semi-definite functional and then to determine the free energy from this, rather than the other way around, which would be the traditional approach.
Particularly detailed versions of these formulae are given for the model with two memory contributions in the free energy, the first being the well-known quadratic functional leading to constitutive relations with linear history terms, while the second is a quartic functional yielding a cubic term for the stress function memory dependence. Also, the discrete spectrum model, for which each memory kernel is a sum of exponentials, is generalized from the quadratic functional representation for the free energy to that with the quartic functional included.
Finally, a model is considered, allowing functional power series with an infinite number of terms for the free energy, rate of dissipation and stress function.
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1 Introduction
We consider a material with memory, where the independent field variable will be referred to as the strain function. It is taken to be a scalar quantity, for simplicity.
The general representation of a free energy of this material is a functional of the history of strain and a function of the current strain. We assume that this functional can be expanded as a finite or infinite functional Taylor expansion in the history of strain. The most general expansion of this kind has a dependence on the current strain in each kernel of the expansion. This dependence is neglected in the model considered here. The stress function is derivable from the free energy.
What we are dealing with in general is a nonlinear viscoelastic material. The linear memory/quadratic free energy model will be referred to as the linear model. Since the general formulae are quite complicated, the case involving one extra term beyond the linear model will be stated in full, including the linear model terms.
The results presented, or generalizations of these results to tensor form, should have practical applications in the context of numerical analysis of the mechanical behaviour of nonlinear materials with memory. Also, re-interpretation of the strain and stress functions as other physical quantities, combined in some cases with one or two minor changes, broadens the application range to include other thermodynamic systems, such as heat conductors and electromagnetic materials.
Relations within an equation number are referred to by counting the number of =, <, > etc.
Thermodynamical constraints [1] on the theory are not discussed in this work. This is an important topic, requiring separate investigation.
2 Properties of Kernels
The current value of the strain function is \(E(t)\) while the strain history and some relative histories are given by
Equation (2.1)3 differs from (2.1)2 only by a change of notation, but is included to emphasize that the relative strain is not always defined with respect to the current time \(t\). The simple property
will be used later. It is assumed here that
which simplifies certain formulae. Note also that
The stress function is given by \(T(t) = \tilde{T}(E^{t},E(t))\), while we denote a particular free energy at time \(t\) by \(\psi (t) = \tilde{\psi }(E^{t},E(t))\), where \(\tilde{T}(E^{t},E(t))\) and \(\tilde{\psi }(E^{t},E(t))\) are understood to be functionals of \(E^{t}\) and functions of \(E(t)\). Certain properties of free energies were derived in [2] and used to characterize such quantities in [3–5] and elsewhere. They have been referred to as the Graffi [6] definition of (or conditions for) a free energy and are given as follows. Let \(\psi (t) = \tilde{\psi }(E^{t},E(t))\) be a free energy. Then
- P1::
-
$$ \frac{\textstyle \partial }{\textstyle \partial E(t)}\tilde{\psi }(E^{t},E(t)) = \frac{\textstyle \partial }{\textstyle \partial E(t)}\psi (t) = T(t). $$(2.5)
- P2::
-
For any history \(E^{t}\)
$$ \tilde{\psi }(E^{t},E(t)) \geq \tilde{\phi }(E(t)) \;\; \mbox{or} \;\; \psi (t) \geq \phi (t), $$(2.6)where \(\phi (t)> 0\) is the equilibrium value of the free energy \(\psi (t) \), defined as
Thus, equality in (2.6) is achieved for equilibrium conditions. Observe that the classical elastic energy \(\phi (t)\) is always taken to be positive so that, from (2.6), the quantity \(\psi (t)\) also has this property.
- P3::
-
It is assumed that \(\psi \) is differentiable. For any \((E^{t},E(t))\) we have the first law (balance of energy)
$$ \dot{\psi }(t) + D(t) = T(t)\dot{E}(t), $$(2.7)where \(D(t)\geq 0\) is the rate of dissipation of energy associated with \(\psi (t)\). This nonnegativity requirement on \(D(t)\) is an expression of the second law.
The basic condition is P3. Relations P1 and P2 follow from P3.
Integrating (2.7) over \((-\infty ,t]\) yields that
The quantity \(W(t)\) is the work function, while \({\mathcal{D}}(t)\) is the total dissipation resulting from the entire history of deformation of the body. It is assumed that the integrals in (2.8) are finite. In particular, we must have
with a similar assumption for \({\mathcal{D}}(t)\). The time derivative of \(\tilde{\psi }(E^{t},E(t))\) consists of the ordinary time derivative of the \(E(t)\) dependence, giving, with the aid of (2.5),
and a functional derivative of the history dependence \(E^{t}\), which yields the dissipation. Note that (2.10) follows from (2.8)4.
Let us now briefly demonstrate that the work function also obeys P1, using a somewhat modified version of the argument in [2], and P2. We can write
where the rightmost term is a Fréchet differential of \({\widetilde{W}}\), defined within a suitable Hilbert space (for example [1], page 104). Thus, (2.10) can be written in the form
The quantity \(\dot{E}(t)\) can take arbitrary values, so that (2.5) or P1 must hold for \(\tilde{\psi }\) replaced by \({\widetilde{W}}\). Thus, we have
giving
It follows that
Also, the quantity \(\delta {\widetilde{W}}\) must vanish.
Note that (2.8)1 implies
2.1 Kernels of Free Energy Terms
The following functions are introduced:
The quantity \(N\) is a positive integer, which may be infinite. If it is infinite, convergence assumptions must be included for the series involved. The superscript on \(G\) indicates the total number of arguments. We shall argue below that, for even \(k\), these may be the kernels of a free energy, while for odd \(k\), a particular choice of these quantities may define the stress function derived from the free energy (see (2.5)).
The quantities \(G^{(k)}\) \(k=1,2, \ldots , N\) and related functions introduced below first enter the model by their occurrence in integrals of the form
where the single integral sign here and below is understood to mean as many integral signs as there are \(d u_{1}\), \(d u_{2}\) etc. The function \(f(u)\), which is always related to the strain history, can be chosen arbitrarily, subject to the requirement that the integral exists. Note that
which follows by using the standard device of renaming integration variables. A similar property holds for any permutation of \(u_{1}, u_{2}, \dots , u_{k}\). The important property here is the complete symmetry of the product of \(f(u_{i})\). Thus, only the totally symmetric part of the kernel contributes to the integral. For simplicity, we assume that
and similarly for any other permutation. In other words, we take \(G^{(k)}\) \(k=1,2, \ldots , N\) and similar related quantities to be completely symmetric in all their arguments.
For odd \(k\), the functional of \(f(u)\) given by (2.18) changes sign if \(f(u)\) is replaced by \(-f(u)\), so that it cannot be positive definite or semi-definite for all choices of \(f(u)\). If \(k\) is even, then this non-negativity property can hold, provided certain restrictions are imposed on the kernel.
We only consider free energies consisting of terms with even \(k\); the constraints on the kernels to guarantee non-negativity are assumed to hold. Each term separately will be non-negative. Equation (2.5) then gives that the stress function will only consist of terms with odd \(k\).
It is assumed that the quantities \(G^{(k)}({\mathbf {u}}^{(k)})\), similar kernels introduced below and indeed the strain histories, have differentiability properties as required in the various contexts discussed in this work.
The constants \(G^{(k)}_{\infty }\) are given by
where \(j\) is any integer in the set \(\{1,2,\ldots ,k\}\). The fact that this quantity is the same for every \(j\) is an expression of the complete symmetry of the dependence of \(G^{(k)}\) on its parameters. We illustrate this with the case \(k=2\), where \(G^{(2)}(u_{1},u_{2})\) is converging to let us say \(G_{1}\) if the first argument is very large and \(G_{2}\) if the second is very large. The symmetry property \(G^{(2)}(u_{1},u_{2})=G^{(2)}(u_{2},u_{1})\) gives that \(G_{2}=G_{1}\).
The quantities \(G^{(k)}_{\infty }\) are non-negative. Let us define
where a subscripted integer \(j\) indicates partial differentiation with respect to the corresponding \(u_{j}\). Thus
where the operator \(\partial _{j}\) is the partial derivative \(\frac{\textstyle \partial }{\textstyle \partial u_{j}}\).
The convergence of the integral (2.19)1 is better at large \(u_{j}\) if \(G^{(k)}(u_{1},u_{2},\dots ,u_{k})\) is replaced by \({\widetilde{G}}^{(k)}(u_{1},u_{2},\dots ,u_{k})\).
Consider the function space \({\mathcal{F}}^{(k)}\), where \(k\) is even, with a norm
This is a non-negative, finite quantity, as indicated. We assume that the function \(f\), which in this context is always related to strain history, belongs to the function space
where \(N\) is even and \({\mathcal{F}}^{(0)}\) contains functions without history dependence, specifically the quantities \(\phi (t)\), defined by (3.3) below, with \(E(t)\) replaced by \(f(t)\).
2.2 The Kernels of the Rate of Dissipation Terms
We also define the functions
which will be shown to be the negative of the kernels making up the rate of dissipation \(D(t)\), introduced in (2.7). These kernels are defined only for the positive even integers. They have the property that
where \(k=2,4, \dots , 2 N\).
A difficulty in constructing free energy functionals arises in making choices that ensure nonnegative functional forms both for the free energy and for the rate of dissipation. A method, proposed in the context of the linear model [7], which renders this task more straightforward, is generalized below to higher terms. Instead of constructing the free energy and determining from this the rate of dissipation, which may not have the required nonnegativity, the procedure is reversed, which guarantees a satisfactory free energy functional [7] (see also [1], pg. 394). One chooses a nonnegative functional for the rate of dissipation. Formulae are presented below which give the associated free energy functional in terms of the dissipation rate kernel. It emerges that the resulting free energy has the required nonnegativity property.
Proposition 2.1
Let us assume that we know the form of the quantities \(K^{(k)}({\mathbf {u}}^{(k)})\) and that they have the required nonnegativity property, namely
for arbitrary \(f\). Then the kernels \(G^{(k)}({\mathbf {u}}^{(k)})\) are determined by
and they have the required nonnegativity properties.
Proof
It follows from (2.29) that
which is (2.26). We have
Let us put
for arbitrary choices of \(f(u)\). Then,
by virtue of (2.28). It follows that \({\widetilde{G}}^{(k)}({\mathbf {u}}^{(k)})\) has the required non-negativity property. □
There are two equivalent alternatives for the developments outlined below, the first being to use \({\widetilde{G}}^{(k)}({\mathbf {u}}^{(k)})\), \(K^{(k)}({\mathbf {u}}^{(k)})\), \(\dot{E}^{t}(s)\) and the second to use \({\mathcal{G}}^{(k)}({\mathbf {u}}^{(k)})\), \({\mathcal{K}}^{(k)}({\mathbf {u}}^{(k)})\), \(E^{t}_{r}(s)\). Both have been widely adopted in discussing the minimum and related free energies for linear constitutive materials. In the present work, we will mainly present formulae in both notations. Moving from one alternative to the other involves a series of integrations by parts.
We can in fact choose either alternative for each parameter \(u_{i}\), rather than fix on the same choice for all \(u_{i}\), as in (3.1), below. For example, for \(u_{i}\), we could switch from \({\widetilde{G}}^{(k)}({\mathbf {u}}^{(k)})\), \(K^{(k)}({\mathbf {u}}^{(k)})\), \(\dot{E}^{t}(u_{i})\) to \(\partial _{i} G^{(k)}({\mathbf {u}}^{(k)})\), \(\partial _{i} K^{(k)}({\mathbf {u}}^{(k)})\), \(E^{t}_{r}(u_{i})\).
3 The General Form of Free Energy and Dissipation Functionals
We now construct (2.7) for the nonlinear material under consideration.
3.1 Free Energies
For a scalar theory the form of a free energy is given by
The quantity \(\phi (t)\) is the static limit of \(\psi (t)\). The multiplying constants are chosen so the they lead to a constant equal to unity on the stress functionals introduced below. Using (3.1)2, we see that
Note that the kernel \(G^{(2 k)}\) has been used here instead of \({\widetilde{G}}^{(2 k)}\). A simple choice for \(\phi (t)\) in (3.1)1 is given by
and we have
Another version of these formulae, obtained by a change of variables, is given by
where .
Observe, from for example (3.1)3, that \(\psi _{2 k}\) is a polynomial of order \(2 k\) in \(E(t)\). Also, \(\psi (t)=\tilde{\psi }(E^{t}_{r},E(t))\) is a polynomial of order \(2 N\) in \(E(t)\), while the stress function \(T(t)=\tilde{T}(E^{t}_{r},E(t))\), introduced below, is a polynomial of order \(2 N-1\). Examples of these polynomials are given below.
There is a further form for a free energy functional:
where
The first form given for the quantity \(S(t)\) is required to ensure that (2.5) holds. The others result from repeated integrations by parts. The two general terms are
As noted above, all quantities of interest, in the present model, are polynomials in \(E(t)\) of order \(2 N\) or lower, in particular, the stress function \(T(t)\), which is a polynomial of order \(2 N-1\). In this context, we refer to (4.2). Thus, if \(k = 2 N\), the integral and all subsequent terms in (3.8) vanish.
3.2 Dissipation Functionals
The rate of dissipation has the form
A question which immediately arises is what choices of the functions \(K^{(2 k)}({\mathbf {u}}^{(2 k)})\) ensures that \(D(t)\) will be nonnegative? The simplest choice is to assume that \(K^{(2 k)}\) is completely factorizable, giving
so that
This option is discussed further in Sect. 6.
3.3 Non-uniqueness of the Free Energy
The kernels \(G^{(2 k)}({\mathbf {u}}^{(2 k)})\) and \({\mathcal{G}}^{(2 k)}({\mathbf {u}}^{(2 k)})\) are not uniquely given. If we add a term \(G_{1}^{(2 k)}({\mathbf {u}}^{(2 k)})\) to \(G^{(2 k)}({\mathbf {u}}^{(2 k)})\), such that the positivity requirements are preserved but \(G_{1}^{(2 k)}({\mathbf {u}}^{(2 k)})\) has the property
then the functional (3.1) remains a valid free energy, yielding the same stress function. Such a change effects \(K^{(2 k)}({\mathbf {u}}^{(2 k)})\) and \({\mathcal{K}}^{(2 k)}({\mathbf {u}}^{(2 k)})\) also. This line of argument suggests that there are typically many free energies and dissipation functionals corresponding to a given constitutive relation for stress. Such properties are known to exist for the linear model (see for example [8]). Discussion of this issue and how to achieve uniqueness may be found in [9].
3.4 The Stress Function
Let \(T(t)\) be the stress at time \(t\), determined by (2.5). Then the constitutive relation has the equivalent forms
An alternative form is
The quantity \(T_{e}(t)\) is the stress function for the equilibrium limit () and the quantity is the linear relaxation function of the material. The quantity \(T_{e}(t)\) in (2.4) is given by
For odd choices of \(k\), the quantities \(G^{(k)}({\mathbf {u}}^{(k)}), {\mathcal{G}}^{(k)}({\mathbf {u}}^{(k)})\), \(k=1,3, \dots ,2 N-1\) are assumed to be nonnegative, as is true for \(k=1\).
Remark 3.1
Condition (2.5) is satisfied provided that
where \(G^{(2 k-1)}({\mathbf {u}}^{(2 k-1)})\) is the kernel in the stress function (see (3.13)) corresponding to \(G^{(2 k)}({\mathbf {u}}^{(2 k)})\). Any kernel with \(2 k-1\) parameters could be indicated by \(G^{(2 k-1)}({\mathbf {u}}^{(2 k-1)})\), but we choose to reserve this notation for those occurring in the definition of stress, obeying (3.16). An alternative form of (3.16) is given by
The assertion in (3.17) may be demonstrated with the aid of (2.2), (3.1)3 and (3.14)1.
Remark 3.2
The kernels \(G^{(2 k-1)}({\mathbf {u}}^{(2 k-1)})\) are assumed to be determined by the material under consideration. In other words, we can determine the kernel by a series of measurements of the stress function, for given strain histories ([10], Chap. 5, Sect. 2). This means that the stress function \(\tilde{T}(E^{t}, E(t))\) and indeed the quantity \(S(t)\), given by (3.7), are uniquely associated with the material. The non-uniqueness associated with \(\psi (t)\) lies in the term after \(S(t)\) in (3.6).
3.5 Symmetry Under Sign Inversion
We have
The stress function derivable from a free energy, in accordance with (2.5), only has odd powers of the stress history, so it has the property that
3.6 The Work Function
Basic properties of \(W(t)\) are
Let . Explicit forms of \(W(t)\) can be expressed as follows:
The second integral sign in (3.21)2 indicates the presence of \(2 k-1\) identical integral signs.
3.7 The Energy Equation
Let us now show that the energy conservation equation (2.7) holds, as a consequence of the above formulae. We use the second form of (3.5) for the free energy. The time derivative acting on the upper limit of the integrals give zero since \(E_{r}(t)=0\). The time derivative acting on the arguments \(t-u_{i}\) can be replaced by \(- \partial _{i}\), while if it is acting on \(E_{r}(u_{2 k})\), we obtain \(- \dot{E}(t)\). In this term, the integral and derivative with respect to the selected variable \(u_{2 k}\) cancel out to give \(u_{2 k}\) a value \(t\) so that \(t-u_{2 k} = 0\). Thus,
The total symmetry between the arguments has been invoked. Using the last relation of (2.26), together with (3.9) and (3.14), we see that (3.22) implies (2.7).
4 Formulae for N=2
We now give the explicit version of a free energy, the corresponding rate of dissipation, together with the work and stress functions, all for \(N=2\).
The following identities make explicit the property referred to above, that all quantities of interest are polynomials in \(E(t)\). In the quadratic case,
while for the quartic terms,
The form of a free energy is
or
Relation (3.7) becomes in this context
Alternatively, using (4.1) and (4.2), together with symmetry properties, relation (4.3) takes the form
where
Note that (4.7)2,4 are examples of (3.16).
We can write \(S(t)\) as a polynomial in \(E(t)\), as follows
For \(N=1\), the case where the stress function is a linear history of the strain, \(S(t)\) takes the form
which is familiar in various contexts [1].
The stress function is given by
where \(G_{\infty }^{(2)}\) and \(G_{\infty }^{(4)}\) are special cases of the quantity introduced in (2.21). We have \({\widetilde{G}}_{2}^{(1)}(u_{1}) = G_{2}^{(1)}(u_{1})-G_{\infty }^{(1)}\) where \(G_{2}^{(1)}(u_{1})\) is the linear relaxation function, while \({\mathcal{G}}_{2}^{(1)}(u_{1})\) is the derivative of this linear relaxation function. Also, \({\widetilde{G}}^{(3)}(u_{1},u_{2},u_{3}) = G^{(3)}(u_{1},u_{2},u_{3})-G_{\infty }^{(3)}\), the quantity \(G^{(3)}(u_{1},u_{2},u_{3})\) being a generalization of the linear relaxation in the context of cubic terms. The definitions of \({\mathcal{G}}_{2}^{(1)}(u_{1})\) and \({\mathcal{G}}^{(3)}(u_{1},u_{2},u_{3})\) in terms of more basic quantities are given in (4.7).
Alternatively, we can write the stress function as
Using (4.10)2, the stress function can be written as a polynomial in \(E(t)\):
Substituting (4.12)1 into (4.5), we obtain
or
These relations could also be derived from (4.8) and (4.12).
The rate of dissipation will now be considered. From (2.26), we see that
Inverses of these relations are given by the following special cases of (2.29)
Equations (4.15)1 and (4.16)1 are familiar from the linear model [1, 7]. Similar relations to (4.15) and (4.16) are true for \({\mathcal{K}}^{(2)},{\mathcal{K}}^{(4)}\) and \({\mathcal{G}}^{(2)},{\mathcal{G}}^{(4)}\).
The rate of dissipation is given by
or
For \(N=2\), the expression (3.21) for the work function can be written as
The quadratic term can be written as
The quantity \(W(t)\) cannot be regarded as a free energy if the property discussed in [11] is taken into account. However, from (2.8), it follows that it must be greater than or equal to the maximum free energy associated with the material, an observation which follows from (2.8) for any free energy \(\psi (t)\). Thus, we have in general the requirement that
5 Discrete-Spectrum Materials
We will give the relevant formulae for \(N = 2\). Generalization to larger values of \(N\) is relatively straightforward. Repeating certain relations from (4.3), we find that
where \(n\) is a positive integer and the inverse decay times \(\alpha _{i}\), \(i=1,2, \ldots , n\), are positive. The quantities with components \(C^{(2)}_{i j}\), \(C^{(4)}_{i j k l}\) must be non-negative on , respectively. This means that if \({\lambda }_{1}\), \(i=1,2 \dots , n\) are the components of a vector in then
for all choices of \({\lambda }_{i}\).
Remark 5.1
We are taking the values of the decay parameters \(\alpha _{j}\), \(j= i,2,\dots , n\) and their total number \(n\) as equal for the quadratic and quartic terms, to avoid proliferation of subscripts and superscripts. In fact, we are free to choose them to be unequal, which can be indicated by assigning extra subscripts or superscripts to these parameters.
Also, from (4.17),
where the summation convention is not in force. The matrices \(\Gamma ^{(2)}_{i j}\), \(\Gamma ^{(4)}_{i j k l}\) are independent of each other (note remark 5.1 in this context), so that, for example, one of them can be put equal to zero, if we wish to focus on the properties of the other.
These quantities \(\Gamma ^{(2)}_{i j}\), \(\Gamma ^{(4)}_{i j k l}\) are assumed to be non-negative in the sense of (5.2). This ensures that the second law \(D(t) \geq 0\) is obeyed. Then, it follows from Proposition 2.1 that \(C^{(2)}_{i j}\), \(C^{(4)}_{i j k l}\) are also positive semi-definite quantities.
Using (4.7), (4.10) and (5.1), we see that the stress function is given by
Thus, we must have
where \(G^{(1)}_{i}\), \(i=1,2, \dots ,n\) are the coefficients of the exponentially decaying terms in the linear relaxation function and \(G^{(3)}_{i j k}\), \(i,j,k=1,2, \dots ,n\) are the corresponding quantities for the cubic nonlinear terms in the constitutive equations. The forms given in terms of \(C^{(2)}_{i j}\) and \(C^{(4)}_{i j k l}\) may be derived from (5.1), together with (4.7)2,4. We note the points made after (4.10), in this context.
The vector \(\mathbf{e}\) in \(\mathbb{R}^{n}\) is defined by [1]
where
The quantities \(E_{+}^{t}(-i\alpha _{i})\) are real. They are the Laplace transforms
We have
Then,
6 Product Formulae for the Rate of Dissipation
Referring to (3.10), (2.29) and (2.27), we look at the case
Let
Also,
where the coefficients \(a_{r}\), \(r= 2,4, \dots \) are assumed to be nonnegative quantities, so that the function \(F(t,z)\) is also nonnegative. If the summations are infinite, we must assume convergence. The form (6.2)3 will be used. Then,
The stress \(T(t)\) emerges from (6.4)5,6,7 and differentiating the term \(E(t)\) in \(E_{r}^{t}(u)=E(t-u)-E(t)\) with respect to \(E(t)\).
Let us check that (2.7) holds. The contribution \(T(t)\dot{E}(t)\) follows from \(T(t)\) determined as above. The quantity \(D(t)\) arises by differentiating \(E^{t}(u)=E(t-u)\) with respect to \(t\) in (6.2)2, treating \(E(t)\) as a constant. This action will be denoted by \(\partial _{d}\). Using the same manipulation as in (2.4), we see that
Then,
so that
Remark 6.1
Observe that discrete spectrum materials, discussed in Sect. 5, are particular examples of (6.1) if the matrices \(\Gamma _{i j}\) and \(\Gamma _{i j k l}\) are factorizable in the sense that
where .
6.1 Exact Summations for a Simple Model
Let us now specialize further to the case where the functions \(d_{2 k}\) are the same for all terms so that
We put
Also,
where the coefficients \(a_{l}\), \(l= 2, 4, 6 \dots \) are assumed to be nonnegative quantities, so that the function \(F(t,z)\) is also nonnegative. Then, the general forms of the rate of dissipation, free energy, total dissipation and stress function are given by the first six relations of (6.4). The general shape of \(D(t)\) should be obtained from experiments. We make a mathematically convenient choice, taking
which gives
where \(C\) is a positive constant. This is zero for vanishing strain and \(C\) for large strain. Thus, using (6.4), we have
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The author thanks Technological University–Dublin for non-financial support during the preparation of this paper. Most recently, this support was supplied by the Environmental Sustainability and Health Institute of the University.
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Golden, J.M. Free Energies for Nonlinear Materials with Memory. J Elast 148, 141–165 (2022). https://doi.org/10.1007/s10659-022-09888-2
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DOI: https://doi.org/10.1007/s10659-022-09888-2